CA2213050A1

CA2213050A1 - Compositions containing thiocarbonates and acylated-nitrogen containing compounds

Info

Publication number: CA2213050A1
Application number: CA002213050A
Authority: CA
Inventors: John S. Manka; James A. Supp; William D. Abraham; Stephen H. Roby
Original assignee: Lubrizol Corp
Current assignee: Lubrizol Corp
Priority date: 1996-08-21
Filing date: 1997-08-15
Publication date: 1998-02-21
Also published as: JPH1088168A; AU3421297A; EP0825247A3; EP0825247A2

Abstract

This invention relates to a composition, comprising: (A) a compound represented by the formula S
¦
R1-X-C-S-(CR2R3)nT (A-I) wherein in Formula (A-I): R1, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;
with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different; and (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms. In one embodiment, the inventive composition further comprises (C) a phosphorus compound. In one embodiment, the inventive composition further comprises (D) an organic sulfide. In one embodiment, the inventive composition further comprises (E) a heterocyclic compound. In one embodiment, the inventive composition further comprises (F) a thiocarbamate. In one embodiment, the invention relates to a process comprising mixing the foregoing components (A) and (B) with an oil of lubricating viscosity, and, optionally, one or more of the foregoing components (C), (D), (E) and/or (F). The inventive compositions are useful in formulating lubricating compositions and functional fluids characterized by enhanced antiwear properties.

Description

- CA 022130~0 1997-08-1~
-Title: COMPOSITIONS CONTAINING THIOCARBONATES AND
ACYLATED-NITROGEN CONTAINING COMPOUNDS

Technical Field Thisinventionrelatestocompositionscontainingthiocarbonates and acylated nitrogen-containing compounds. These compositions are useful in formulating lubricants and functional fluids characterized by enhanced antiwear properties.
Background of the Invention Engine lubricating oils require the presence of additives to protect the engine from wear. For almost 40 years, the principal antiwear additive for engine lubricating oils has been zinc dialkyl dithiophosphate (ZDDP). However, ZDDP is typically used in the lubricating oil at a sufficient concentration to provide a phosphorus content of 0.12% by weight or higher in order to pass required industry standard tests for antiwear. Since phosphates may result in the deactivation of emission control catalysts used in automotive exhaust systems, a reduction in the amount of phosphorus-containing additives (e.g., ZDDP) in the oil would be desirable. The problem sought to be overcome is to provide for a reduction in the amount of phosphorus-containing additive in the lubricating oil and yet provide the lubricating oil with desired antiwear properties. The present invention provides a solution to this problem by providing compositions that can function as either a partial or complete replacement for ZDDP.

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U.S. Patent 2,020,021 discloses the use of thiocarbonates represented by the formulae RO-C(S)-SR1 and RS-C(S)-SRl as lubricant additives for improving the extreme pressure characteristics of lubricants.
U.S. Patents 2,110,281 and 2,206,245 disclose the use of 5xanthic acid esters represented by the formula RO-C(S)-SR as additives for lubricants used on bearing surfaces which are subjected to high pressures and high rubbing velocities during use.
U.S. Patent 5,026,492 discloses the use of alkyl alkoxy alkyl xanthates represented by the formula R1-O-R2-O-C(S)-S-R3 in combination 10with metal thiophosphates as antiwear additives for lubricating oil compositions.
The use of ashless dispersants in lubricants is disclosed in numerous patents, including U.S. Patents 3,172,892; 3,219,666;
3,272,746; 3,310,492; 3,341,542; 3,444,170; 3,455,831; 3,455,832;
153,576,743; 3,630,904; 3,632,511; 3,804,763; and 4,234,435.
The use of metal salts of phosphorodithioic acids as additives for lubricants is disclosed in U.S. Patents 4,263,150; 4,289,635; 4,308,-154; 4,322,479; and 4,417,990. Amine salts of such acids are disclosed as being useful as additives for grease compositions in U.S. Patent 205,256,321.
The use of disulfides represented by the formula (RzYC = S)2S2, wherein Y is O, S or N, and z is 1 when Y is O or S and 2 when Y is N, as lubricant additives is disclosed in U.S. Patents 2,681,316; 2,691,632; and 2,694,682.
25U.S. Patent 2,307,307 discloses the use of compounds represented by the formula (RXC=S)2Sn, wherein X is O or S, and n is greater than 2, as lubricant additives.
The use of compounds represented by the formula (ROC = S)S2 in lubricants for use on bearing surfaces is disclosed in U.S. Patents 2,110,281 and 2,206,245. U.S. Patent 2,431,010 discloses the use of CA 022130~0 1997-08-1~

compounds represented by the formula ~ROC=S)Sn, wherein n is 2-4, as soluble cutting oil additives.
The use of thiuram sulfides as lubricant additives is disclosed in U.S. Patents 2,081,886; 2,201,258; 3,249,542; 3,352,781; 4,207,196;
and 4,501,678.
U.S. Patent 5,034,141 discloses that improved antiwear results can be obtained by combining a thiodixanthogen (e.g., octylthiodixanthogen) with a metal thiophosphate (e.g., ZDDP). U.S. Patent 5,034,142 discloses the addition of a metal alkoxyalkylxanthate (e.g., nickel ethoxyethylxan-thate), a dixanthogen (e.g., diethoxyethyl dixanthogen) and a metal thiophosphate (e.g., ZDDP) to a lubricant to improve antiwear.
European patent application 0 609 623 A1 discloses an engine oil composition containing a metal-containing detergent, zinc dithiophosphate, a boron-containing ashless dispersant, aliphatic amide compound, and either a dithiocarbamate compound or an ester derived from a fatty acid and boric acid. Among the dithiocarbamates that are disclosed are sulfides and disulfides.
U.S. Patent 3,409,635 discloses a process for making cyclic compounds represented by the formula R' R2 Rl _C--~--R2 O~ ,S

S
wherein R1 and R2 are hydrogen or methyl. The reference indicates that the cyclic xanthates are useful as fungicides, and the epithiranes yield polymers which aid in the vulcanization of rubber.
U.S. Patent 3,448,120 discloses a process for making alkylene dithiocarbonates.

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U.S. Patent4,51 1 ,464discloses 1 ,3-oxathiolane-2-thiones and 1 ,3-dithiolane-2-thiones as collectors for concentrating sulfide mineral ores using froth flotation.
U.S. Patent 4,758,362 discloses the addition of a thiocarbamate to a low phosphorus or phosphorus free lubricating oil composition to provide a composition with enhanced extreme-pressure and antiwear properties.
S~..,...~c.r.~ of the Invention This invention relates to a composition, comprising:
(A) a thiocarbonate represented by the formula R1--X--C--S--(CRZR3)nT (A-l~

wherein in Formula (A-l): R~, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;
with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different; and (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms.
In one embodiment, the inventive composition further comprises (C) a phosphorus compound. In one embodiment, the inventive composition further comprises (D) an organic sulfide. In one embodiment, the inventive composition further comprises (E) a heterocyclic compound. In one embodiment, the inventive composition further comprises (F) a thiocarbamate. In one embodiment, the invention relates to a process comprising mixing the foregoing components (A) and (B) with an oil of lubricating viscosity, and, optionally, one or more of the foregoing components (C), (D), (E) and/or (F).

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The inventive compositions are useful in formulating lubricating compositions and functional fluids characterized by enhanced antiwear properties. In one embodiment, these lubricating compositions and functional fluids are characterized by reduced phosphorus levels when compared to those in the prior art, and yet have sufficient antiwear properties to pass industry standard tests for antiwear. In one embodiment, the inventive lubricating compositions are characterized by enhanced extreme pressure properties. In one embodiment, the inventive lubricating compositions are characterized by good seal compatibility. The inventive lubricating compositions are especially suitable for use in lubricating oil compositions for internal combustion engines.
Descri"lion of the ~lef~r,ed Embodiments As used in this specification and in the appended claims, the terms "hydrocarbyl" and "hydrocarbon based" denote a group having a carbon atom directly attached to the remainder of the molecule and having a hydrocarbon or predominantly hydrocarbon character within the context of this invention. Such groups include the following:
(1) Hydrocarbon groups; that is, aliphatic, (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl or cycloalkenyl), aromatic, aliphatic- andalicyclic-substituted aromatic, aromatic-substituted aliphatic and alicyclic groups, and the like, as well as cyclic groups wherein the ring is completed through another portion of the molecule (that is, any two indicated substituents may together form an alicyclic group). Such groups are known to those skilled in the art. Examples include methyl, ethyl, octyl, decyl, octadecyl, cyclohexyl, phenyl, etc.
(2) Substituted hydrocarbon groups; that is, groups containing non-hydrocarbon substituents which, in the context of this invention, do not alter the predominantly hydrocarbon character of the group. Those skilled in the art will be aware of suitable substituents.
Examples include halo, hydroxy, nitro, cyano, alkoxy, acyl, etc.

(3) Hetero groups; that is, groups which, while predominant-ly hydrocarbon in character within the context of this invention, contain atoms other than carbon in a chain or ring otherwise composed of carbon atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for example, nitrogen, oxygen and sulfur.
In general, no more than about three substituents or hetero atoms, and preferably no more than one, will be present for each 10 carbon atoms in the hydrocarbyl group.
Terms such as "alkyl-based," "aryl-based," and the like have meanings analogous to the above with respect to alkyl groups, aryl groups and the like.
The term "hydrocarbon-based" has the same meaning and can be used interchangeably with the term hydrocarbyl when referring to molecular groups having a carbon atom attached directly to the remainder of a molecule.
The term "lower" as used herein in conjunction with terms such as hydrocarbyl, alkyl, alkenyl, alkoxy, and the like, is intended to describe such groups which contain a total of up to 7 carbon atoms.
The term "oil-soluble" refers to a material that is soluble in mineral oil to the extent of at least about one gram per liter at 25~C.
(A) Thiocarbonates The thiocarbonates are compounds represented by the formula 2~ R'--X--C--S--(CR2R3)nT (A-l) wherein in Formula (A~ Rl, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is 0 or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;

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with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different.
The substituent R' is hydrogen or a hydrocarbyl group, but is preferably a hydrocarbyl group. It is generally believed that such hydrocarbyl group is desired in order to provide a measure of oil-solubility to the molecule. However, R1 can be hydrogen, provided the other R groups in the molecule provide sufficient oil solubility to the molecule. In practice this means that at least one R group should be a hydrocarbyl group of at least about 4 carbon atoms. In one embodiment, R1 is a hydrocarbyl group (e.g., aliphatic hydrocarbyl groups such as alkyl groups) of 1 to about 50 carbon atoms, and in one embodiment 1 to about 30 carbon atoms, and in one embodiment 1 to about 18 carbon atoms, and in one embodiment 1 to about 12 carbon atoms.
In one embodiment, R2 and R3 are independently hydrogen or methyl or ethyl groups, with hydrogen being preferred.
In describing T as an "activating group," what is meant is a group which will activate an olefin to which it is attached toward nucleophilic addition by CS2. (This is reflective of a method by which this material can be prepared, by reaction of an activated olefin with CS2 and a mercaptan or an alcohol.) The activating group T can be, for instance, an ester group, typically but not necessarily a carboxylic ester group of the structure -COOR. It can also be an ester group based on a non-carbon acid, such as a sulfonic or sulfinic ester or a phosphonic or phosphinic ester. The activating group can also be any of the acids corresponding to the aforementioned esters. T can also be an amide group, that is, based on the condensation of an acid group, preferably a carboxylic acid group, with an amine. In that case the -(CR2R3)nT group can be derived from acrylamide.
T can also be an ether group, -OR; a carbonyl group, that is, an aldehyde or a ketone group; a cyano group, -CN, or an aryl group.
In one embodiment, T is -R, -OR, -R*OR, -COR, -COOR, -R*COR, -R*COOR, -CONRR, -R*CONRR, -COO(R*O)tR, -R*COO(R*O)tR, -CN, -R*CN, CA 022130~0 1997-OX-l~

O O O O
Il 11 11 11 -SR, -R*SR, -SOR, -R*SOR, O O O O
11 ll ll ll -SR, -R*SR, -S-OR, -R *S-OR

O O O O

wherein each R is independently hydrogen or a hydrocarbyl group, and each R* is independently a hydrocarbylene or hydrocarbylidene group, and t is number of at least 1. The R groups are hydrogen or hydrocarbyl groups generally having from 1 to about 30 carbon atoms, and in one embodiment 1 to about 18 carbon atoms, and in one embodiment 1 to about 12 carbon atoms. Examples include methyl, ethyl, propyl, n-butyl, isobutyl, pentyl, isopentyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, dodecyl, and the corresponding hydroxy-substituted hydrocarbyl groups such as hydroxymethyl, hydroxyethyl, hydroxypropyl, etc. The R * groups are preferably alkylene or alkylidene groups of 1 to about 8 carbon atoms, and in one embodiment 1 to about 4 carbon atoms, and in one embodiment 2 or 3 carbon atoms. Alkylene groups such as ethylene and propylene are especially preferred. t is a number in the range of about 1 to about 30, and in one embodiment 1 to about 20, and in one embodiment 1 to about 12 and in one embodiment 1 to about 8.
In one embodiment, the thiocarbonate is a compound represented by the formula CA 022130~0 1997-08-1~

R1_X--C--S--R (A-ll) wherein in Formula ~A-ll), Rl and R are independently hydrogen or hydrocarbyl groups as discussed above, and X is 0 or S.
In one embodiment, the thiocarbonate is a compo-~nd represented by the formula S ' O
Il 11 Rl_X--C--S--R7 C--O(R30)tR4 (A-lll) wherein in Formula (A-lll): R' and R4 are independently hydrogen or hydrocarbyl groups; R2 and R3 are independently hydrocarbylene or hydrocarbylidene groups; X is 0 or S; and t is a number in the range of 1 to about 12, and in one embodiment 1 to about 8. In one embodiment, R1 and R4 are independently hydrogen or hydrocarbyl groups of 1 to about 50 carbon atoms, and in one embodiment 1 to about 30 carbon atoms, and in one embodiment 1 to about 18 carbon atoms. In one embodiment, R2 and R3 are independently alkylene or alkylidene groups of 1 to about 8 carbon - atoms, and in one embodiment 1 to about 4 carbon atoms, and in one embodiment 2 or 3 carbon atoms.
The thiocarbonate compounds (A) can be made by reacting a mercaptan or an alcohol with a metal base to form a mercaptide or an alkoxide. The mercaptide or alkoxide is then reacted with CS2, or a source material for CS2, to form a thiocarbonate salt represented by the formula S
(R'-X-C-S-)8Ta (A-IV) wherein in Formula (A-lVl, R~ and X are as defined in Formula (A-l), T is a metal, and a is the valence of the metal T. T can be a metal selected from the group consisting of Group IA, IIA or IIB metals, aluminum, tin, iron, cobalt, lead, molybdenum, manganese, nickel, antimony, bismuth, or a CA 022130~0 1997-08-1~

mixture of two or more thereof. Sodium is especially useful. In one embodiment, the thiocarbonate salt represented by Formula (A-IV) is useful as component (A) of the invention. In one embodiment, the thiocarbonate salt is further reacted with an additional reactant to form the structure represented by Formula (A-l). This additional reactant is, in one embodiment, an activated olefin, an hydrocarbyl halide (e.g., chloride, bromide), epoxide, or an olefin in combination with an acid catalyst (e.g., HCI) .
The mercaptans that can be used include the hydrocarbyl mercaptans represented by the formula R1-S-H, wherein R1 is as defined above in Formula (A-l). In one embodiment, R' is an alkyl, an alkenyl, cycloalkyl, or cycloalkenyl group. R1 may be an aryl (e.g., phenyl, naphthyl), alkylaryl, arylalkyl or alkylaryl alkyl group. R1 may also be a haloalkyl, hydroxyalkyl, or hydroxyalkyl-substituted (e.g., hydroxymethyl, hydroxyethyl, etc.) aliphatic group. In one embodiment, R' contains from about 1 to about 30 carbon atoms, or from about 2 to about 24, or from about 3 to about 18 carbon atoms. Examples include butyl mercaptan, amyl mercaptan, hexyl mercaptan, octyl mercaptan, 1-octanethiol, 6-hydroxymethyloctanethiol, nonyl mercaptan, decyl mercaptan, 10-amino-dodecanethiol, dodecyl mercaptan, t-dodecyl mercaptan, 1 O-hydroxymethyl-tetradecanethiol, and tetradecyl mercaptan.
The alcohols that can be used include isopropyl, methyl propyl, n-butyl, isobutyl, amyl, 4-methyl-2-pentyl, hexyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodeceny!, aromatic alcohols such as the phenols, etc. Higher synthetic monohydric alcohols of the type formed by Oxo process (e.g., 2-ethylhexyl), the Aldol condensation, or by organo- aluminum catalyzed oligomerization of alpha-olefins (especially ethylene), followed by oxidation and hydrolysis, also are useful. Examples of useful monohydric alcohols and alcohol mixtures include the commercially available "Alfol"
alcohols marketed by Continental Oil Corporation. Alfol 810 is a mixture of alcohols containing primarily straight chain, primary alcohols having from 8 to 10 carbon atoms. Alfol 12 is a mixture of alcohols containing mostly C12 CA 022130~0 1997-08-1~

fatty alcohols. Alfol 1218 is a mixture of synthetic, primary, straight-chain alcohols containing primarily 12 to 18 carbon atoms. The Alfol 20 +
alcohols are mixtures of Cl8-C28 primary alcohols having mostly, on an alcohol basis, C20 alcohols as determined by GLC (gas-liquid-chromato-graphy). The Alfol 22+ alcohols are Cl8-C28 primary alcohols containing primarily, on an alcohol basis, C 2 alcohols. These Alfol alcohols can contain a fairly large percentage (up to 40% by weight) of paraffinic compounds which can be removed before the reaction if desired.
Another example of a commercially available alcohol mixture is Adol 60 which comprises about 75% by weight of a straight chain C22 primary alcohol, about 15% of a C20 primary alcohol and about 8% of C18 and C24 alcohols. Adol 320 comprises predominantly oleyl alcohol. The Adol alcohols are marketed by Ashland Chemical.
A variety of mixtures of monohydric fatty alcohols derived from naturally occurring triglycerides and ranging in chain length of from C8 to C18 are available from Proctor & Gamble Company. These mixtures contain various amounts of fatty alcohols containing mainly 12, 14, 16, or 18 carbon atoms. For example, CO-1214 is a fatty alcohol mixture containing 0.5% of C10 alcohol, 66.0% of C12 alcohol, 26.0% of C14 alcohol and 6.5%
of C16 alcohol.
Another group of commercially available mixtures include the "Neodol" products available from Shell Chemical Co. For example, Neodol 23 is a mixture of C12 and C13 alcohols; Neodol 25 is a mixture of C12 and C15 alcohols; and Neodol 45 is a mixture of C14 to C15 linear alcohols.
Neodol 91 is a mixture of Cg, C10 and C11 alcohols.
Fatty vicinal diols also are useful and these include those available from Ashland Oil under the general trade designation Adol 1 14 and Adol 158. The former is derived from a straight chain alpha olefin fraction of C11-C14, and the latter is derived from a C15-C18 fraction.

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The metal in the metal base can be a metal selected from the group consisting of Group IA, IIA or IIB metals, aluminum, tin, iron, cobalt, lead, molybdenum, manganese, nickel, antimony, bismuth, or a mixture of two or more thereof. The metal base can be a nitrate, nitrite, halide, carboxylate, phosphate, phosphite, sulfate, sulfite, carbonate, borate, hydroxide or oxide. Sodium hydroxide is a preferred metal base.
The relative amounts of the reactants used to prepare the thiocarbonate salts are not particularly critical. The charge ratios to the reactor can vary over a wide range where economics and the amount of the product desired are controlling factors. Thus, in one embodiment, the charge ratio of the mercaptan or alcohol to the CS2 reactant to metal base may vary from about 5:1:1 to about 1:6:1 to about 1:1:5. In one embodiment, the charge ratio of these reactants is about 1:1:1.
The activated olefins, hydrocarbyl halides, epoxides and olefins that can be used as the additional reactant include compounds generally containing from 1 carbon atom in the case of hydrocarbyl halides, or 2 carbon atoms in the case of activated olefins, epoxides or olefins, up to about 30 carbon atoms, and in one embodiment up to about 18 carbon atoms, and in one embodiment up to about 12 carbon atoms. These include hydrocarbon compounds and hydroxy-substituted hydrocarbon compounds.
The activated olefins that can be used include ethylenically-unsaturated carboxylic acids, or alpha-chloro or alpha-bromo carboxylic acids, or derivatives thereof. These include acrylic acid, methacrylic acid, methylacrylate, ethylacrylate, 2-ethylhexylacrylate, 2-hydroxyethylacrylate, ethylmethacrylate, 2-hydroxyethylmethacrylate, 2-hydroxy-propylmethacrylate, 2-hydroxypropylacrylate, acrylamide, acrylonitrile, ethylsulfonylethene, methylsulfinylethene, and the like. Also, alpha-chloroacetic acid and alpha-bromoacetic acid and derivatives thereof can be used.

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The hydrocarbyl halides can be alkyl halides. These include the methyl, ethyl, propyl, n-butyl, isobutyl, pentyl, isopentyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl and dodecyl chlorides and bromides, as well as the corresponding hydroxy-substituted hydrocarbyl chlorides and bromides such as the hydroxymethyl, hydroxyethyl and hydroxylpropyl chlorides and bromides.
The epoxides include: ethylene oxide; propylene oxide; 1,2-epoxyhexane; 1 ,2-epoxyhexadecane; 1 ,2-epoxybutane; 3,4-epoxyheptane;
1,2-epoxy-cyclohexane; 4,5-epoxydecane; 1,2-epoxydodecane; 1,2-epoxytetradecane; 1 ,2-epoxy-5-oxy-heptane; 1 ,2-epoxy-6-propyltridecane;
oxetanes; 9,1 0-epoxystearic acid esters; styrene oxides; para-chlorostyrene oxide; and mixtures of two or more of these.
Also included are the epoxidized fatty acid esters. Typical fatty acid esters include C1 20 alkyl esters of C8.24 unsaturated fatty acids such as palmitoleic, oleic, ricinoleic, petroselic, linoleic, linolenic, oleostearic, licanic, etc. Specific examples of the fatty acid esters which can be epoxidized include lauryl tallate, methyl oleate, lauryl oleate, cetyl oleate, cetyl linoleate, lauryl ricinoleate, oleyl linoleate, oleyl stearate and alkyl glycerides. Also useful are the saturated fatty acid esters prepared from mixed unsaturated fatty acid esters such as are obtained from animal fats and vegetable oils including tall oil, linseed oil, olive oil, castor oil, soybean oil, peanut oil, rape seed oil, fish oil, sperm oil, etc.
The olefins that can be used include aliphatic compounds, alicylic compounds, aliphatic- and alicyclic-substituted aromatic compounds, and the like. These include ethene, propene, butene, isobutene, pentene, hexene, styrene, and the like.
The relative amounts of the reactants used to prepare the thiocarbonate compounds (A) is not particularly critical. The charge ratios to the reactor can vary over a wide range where economics and the amount of the product desired are controlling factors. Thus, the charge ratio of the thiocarbonate salt to additional reactant (e.g., activated olefin, hydrocarbyl -CA 022130~0 1997-08-1~

halide, epoxide or olefin) may vary from about 5:1 to about 1:5. In one embodiment, the charge ratio of these reactants is about 1:1.
A number of methods for preparing trithiocarbonates are disclosed in the article by H.C. Godt Jr., et al. entitled "The Synthesis of Organic Trithiocarbonates", Journal of Organic Chemistry, Vol. 26, October 1961, pp. 4047-4051, which is incorporated herein by reference. Briefly, this article discloses a number of methods for preparing trithiocarbonates.
One method involves reacting an aryl- or alkylthiol in the presence of a base (e.g., NaOH) with an alkyl or aryl chlorodithioformate. Another method involves reacting an alkylthiol with carbon disulfide in the presence of potassium hydroxide to form a potassium alkyl trithiocarbonate, then reacting the latter with an alkyl or aralkyl bromide to form the desired trithiocarbonate. Another method involves reacting thiophosgene with an aryl thiol in the presence of a base to form diaryl trithiocarbonates. Another method involves reacting m-nitro phenyldiazonium chloride with potassium ethyl trithiocarbonate to form m-nitro phenyl trithiocarbonate.
The following examples illustrate the preparation of the thiocarbonate compounds (A) that are useful with the invention. In the following examples, as well as throughout the specification and in the claims, unless otherwise indicated, all parts and percentages are by weight, all temperatures are in degrees Celsius, and all pressures are atmospheric.
Examr~le A-1 t-Dodecyl mercaptan (606 grams), a 50% aqueous solution of sodium hydroxide (240 grams) and toluene (250 grams) are charged to a reactor and heated at 110-130~C until the water is removed. Carbon disulfide (251 grams) is added. The temperature of the mixture is maintained below 50~C using an ice bath during the carbon disulfide addition. The mixture is heated to 1 1 0~C to remove water. The mixture is cooled to 50~C. Propylene oxide (191.4 grams) is added. A 38% by weight aqueous solution of hydrochloric acid (330 grams) is added dropwise.
The resulting organic layer is decanted, filtered and stripped at 110~C and CA 022130~0 1997-08-1~

20 mm Hg to provide the desired product which is in the form of a brown liquid .
Examole A-2 t-Dodecyl mercaptan (912 grams), a 50% aqueous solution of sodium hydroxide (362 grams) and toluene (900 grams) are charged to a reactor and heated at 1 20~C with a nitrogen purge until 240 grams of water are removed. Carbon disulfide (377 grams) is added. The temperature of the mixture is maintained at 50~C using an ice bath during the carbon disulfide addition. The mixture is stripped at 110~C and 20 mm Hg. The mixture is cooled to room temperature and filtered through diatomaceous earth to provide the desired product which is in the form of a red viscous liquid .
Exa~.~Ple A-3 1-Butanol (222 grams), and a 50% aqueous sodium hydroxide 1 5 solution (240 grams) are charged to a reactor and heated to 1 00~C until the water is removed. The reaction mixture is cooled to ~0~C. Carbon disulfide (251 grams) is added. Acrylic acid (216 grams) is added with the result being the formation of a gel. Acetone (400 grams) is added to disperse the gel with the result being the formation of a two-layered mixture. The upper layer is an orange liquid, and the lower layer is a dark red liquid. The upper layer is separated from the lower layer, and acetone is stripped from the upper layer to provide the desired product which is in the form of a gel.
Example A-4 t-Dodecyl mercaptan (808 grams), a 50% aqueous solution of sodium hydroxide (320 grams) and toluene (200 grams) are charged to a reactor and heated at 110-130~C until 106 grams of water are removed.
The mixture is cooled to 50~C. Carbon disulfide (334 grams) is added. The mixture is heated to 1 1 0 ~ C, then allowed to cool. 2-Hydroxyethylacrylate (464 grams) is added. The mixture is cooled to below 50~C. A 38% by weight aqueous solution of hydrochloric acid (440 grams) is added dropwise. Water is separated from the reaction mixture. The mixture is CA 022130~0 1997-08-1~

filtered and stripped at 110-130~C and 20 mm Hg to provide the desired product which is in the form of a yellow-brown liquid.
ExamDle A-5 t-Dodecyl mercaptan (404 grams), a ~0% aqueous solution of sodium hydroxide (160 grams) and toluene (100 grams) are charged to a reactor and heated to 120~C with a nitrogen purge to remove water. The mixture is cooled to room temperature. Carbon disulfide (167 grams) is added. The mixture is heated to 70~C. 2-Hydroxyethylacrylate (232 grams) is added. The mixture is maintarned at 70~C for one hour. The mixture is cooled to room temperature. A 38% by weight aqueous solution of hydrochloric acid (220 grams) is added. One liter of water is added. An organic layer is formed. The organic layer is drawn off and stripped at 70~C
and 20 mm Hg and filtered through diatomaceous earth to provide the desired product which is in the form of a liquid.
1 5 ExamPle A-6 t-Dodecyl mercaptan (404 grams), a 60% aqueous solution of sodium hydroxide (160 grams) and toluene (500 grams) are charged to a reactor and heated at 1 18-1 30~C to remove water. The mixture is cooled to ~0~C. Carbon disulfide (168 grams) is added dropwise. The mixture is heated to 110~C, then allowed to cool. Methylacrylate (172 grams) is added dropwise. The temperature of the mixture increases exothermically.
A 38% by weight aqueous solution of hydrochloric acid (200 grams) is added dropwise. Water is separated from the reaction mixture. The mixture is filtered and stripped at 110-150~C and 20 mm Hg for two hours to provide the desired product which is in the form of a yellow liquid.
Exsr..,,le A-7 t-Dodecyl merca~ t~,- (404 grams), MoO3 (144 grams) and water (10 grams) are charged to a reactor. Carbon disuifide (167 grams) is added.
A 50% by weight aqueous solution of sodium hydroxide (trace amount) is added. The reaction mixture turns purple. The mixture is heated to 60~C
and the desired product, which is in the form of a mixture of blue solid and a green liquid, is formed.

ExamPle A-8 t-Dodecyl mercaptan (404 grams), a 50% aqueous solution of sodium hydroxide (160 grams) and toluene (200 grams) are charged to a reactor and heated at 110-150~C until 104 grams of water are removed.
The mixture is cooled to 50~C. Carbon disulfide (168 grams) is added.
Acrylic acid ( 144 grams) is added. The temperature of the mixture increases exothermically. The formation of a solid green mass is observed. A 37%
by weight aqueous solution of hydrochloric acid (200 grams) is added. An aqueous layer and an organic layer are formed. The aquous layer is separated from the organic layer. The organic layer is stripped at 1 1 0~C and 20 mm Hg to provide the desired product which is in the form of an orange liquid .
Examole A-9 t-Dodecyl mercaptan (2590 grams), a 50% aqueous solution of sodium hydroxide (515 grams) and toluene 12000 grams) are charged to a reactor and heated to 100~C to remove water. The mixture is cooled to room temperature. Carbon disulfide (1070 grams) is added dropwise. The mixture is heated to 70~C and maintained at that temperature with stirring for four hours. The mixture is filtered through diatomaceous earth to provide the desired product which is in the form of a red liquid.
ExamPle A-10 Part A
Hexadecyl mercaptan (2156 grams), a 50% aqueous solution of sodium hydroxide (735 grams) and toluene (1000 grams) are charged to ~5 a reactor and heated at 1 20~C until 464 grams of water are removed. The mixture is cooled to 60~C. Carbon disulfide (698 grams) is added. The mixture is stripped at 1 20~C and 20 mm Hg and filtered through diatornaceous earth to provide the desired product which is in the form of a red liquid.
Part B
The product from Part A (350 gramsJ is placed in a reactor and propylene oxide (57 grams) is added dropwise. The temperature of the CA 022130~0 1997-08-1~

mixture increases exothermically. The mixture is heated to 70~C and maintained at that temperature for two hours. The mixture is filtered through diatomaceous earth to provide the desired product which is in the form of a liquid.
ExamPle A-11 Hexadecyl mercaptan (201 grams), a 50% aqueous solution of sodium hydroxide 168 grams) and toluene (100 grams) are charged to a reactor and heated at 110~C until 42 grams of water are removed. The mixture is cooled to 60~C. Carbon disulfide 165 grams) is added. The temperature of the mixture is maintained at 60~C for three hours. The mixture is stripped at 1 20~C and 20 mm Hg for three hours. The mixture is filtered through diatomaceous earth to provide the desired product which is in the form of an orange liquid.
(B) Acvlated Nitrogen-CG..tdi--i..g ComPounds The second component of the inventive composition is an acylated nitrogen-containing compound having a substituent of at least about 10 aliphatic carbon atoms. These compounds typically function as ashless dispersants in lubricating compositions.
A number of acylated, nitrogen-containing compounds having a substituent of at least about 10 aliphatic carbon atoms and made by reacting a carboxylic acid acylating agent with an amino compound are known to those skilled in the art. In such compositions the acylating agent is linked to the amino compound through an imido, amido, amidine or salt linkage. The substituent of at least about 10 aliphatic carbon atoms may be in either the carboxylic acid acylating agent derived portion of the molecule or in the amino compound derived portion of the molecule. Preferably, however, it is in the acylating agent portion. The acylating agent can vary from formic acid and its acyl derivatives to acylating agents having high molecular weight aliphatic substituents of up to about 5,000, 10,000 or 20,000 carbon atoms. The amino compounds are characterized by the presence within their structure of at least one HN < group.

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ln one embodiment, the acylating agent will be a mono- or polycarboxylic acid (or reactive equivalent thereof) such as a substituted succinic or propionic acid and the amino compound is a polyamine or mixture of polyamines, most typically, a mixture of ethylene polyamines. The amine also may be a hydroxyalkyl-substituted polyamine. The aliphatic substituent in such acylating agents typically averages at least about 30 or at least about 50 and up to about 400 carbon atoms.
Illustrative hydrocarbon based groups containing at least 10 carbon atoms are n-decyl, n-dodecyl, tetrapropylene, n-octadecyl, oleyl, chlorooctadecyl, triicontanyl, etc. Generally, the hydrocarbon-based substituents are made from homo- or interpolymers (e.g., copolymers, terpolymers) of mono- and di-olefins having 2 to 10 carbon atoms, such as ethylene, propylene, 1-butene, isobutene, butadiene, isoprene, 1-hexene, 1-octene, etc. Typically, these olefins are 1-monoolefins. The substituent can also be derived from the halogenated (e.g., chlorinated or brominated) analogs of such homo- or interpolymers. The substituent can, however, be made from other sources, such as monomeric high molecular weight alkenes (e.g., 1-tetracontene) and chlorinated analogs and hydrochlorinated analogs thereof, aliphatic petroleum fractions, particularly paraffin waxes and cracked and chlorinated analogs and hydrochlorinated analogs thereof, white oils, synthetic alkenes such as those produced by the Ziegler-Natta process (e.g., poly~ethylene) greases) and other sources known to those skilled in the art. Any unsaturation in the substituent may be reduced or eliminated by hydrogenation according to procedures known in the art.
Thehydrocarbon-basedsubstituentsaresubstantiallysaturated, that is, they contain no more than one carbon-to carbon unsaturated bond for every ten carbon-to-carbon single bonds present. Usually, they contain no more than one carbon-to-carbon non-aromatic unsaturated bond for every 50 carbon-to-carbon bonds present.
The hydrocarbon-based substituents are also substantially aliphatic in nature, that is, they contain no more than one non-aliphatic moiety Icycloalkyl, cycloalkenyl or aromatic) group of 6 or less carbon atoms CA 022130~0 1997-08-1~

for every 10 carbon atoms in the substituent. Usually, however, the substituents contain no more than one such non-aliphatic group for every 50 carbon atoms, and in many cases, they contain no such non-aliphatic groups at all; that is, the typical substituents are purely aliphatic. Typically, thesepurely aiiphatic substituents are alkyl or alkenyl groups.
Specific examples of the substantially saturated hydrocarbon-based substituents containing an average of more than 30 carbon atoms are the following:
a mixture of poly(ethylene/propylene) groups of about 35 to about 70 carbon atoms a mixture of the oxidatively or mechanically degraded poly(ethylene/propylene) groups of about 35 to about 70 carbon atoms a mixture of poly(propylene/1-hexene) groups of about 80 to about 150 carbon atoms a mixture of poly(isobutene) groups having an average of about 50 to about 200 carbon atoms A useful source of the substituents are poly(isobutene)s obtained by polymerization of a C4 refinery stream having a butene content of about 35 to about 75 weight percent and isobutene content of about 30 to about 60 weight percent in the presence of a Lewis acid catalyst such as aluminum trichloride or boron trifluoride. These polybutenes contain predominantly ~greater than 80% of total repeating units) isobutene repeating units of the configuration In one embodiment, the carboxylic acid acylating agent is a hydrocarbon substituted succinic acid or anhydride. The substituted CA 022130~0 1997-08-1~

succinic acid or anhydride consists of hydrocarbon-based substituent groups and succinic groups wherein the substituent groups are derived from a polyalkene, said acid or anhydride being characterized by the presence within its structure of an average of at least about 0.9 succinic group for each equivalent weight of substituent groups, and in one embodiment about 0.9 to about 2.5 succinic groups for each equivalent weight of substituent groups. The polyalkene generally has an (Mn) of at least about 700, and in one embodiment about 700 to about 2000, and in one embodiment about 900 to about 1800. The ratio between the weight average molecular weight (Mw) and the (Mn) (that is, the Mw/Mn) can range from about 1 to about 10, or about 1.5 to about 5. In one embodiment the polyalkene has an Mw/Mn value of about 2.5 to about 5. For purposes of this invention, the number of equivalent weights of substituent groups is deemed to be the number corresponding to the quotient obtained by dividing the Mn value of the polyalkene from which the substituent is derived into the total weight of the substituent groups present in the substituted succinic acid. Thus, if a substituted succinic acid is characterized by a total weight of substituent group of 40,000 and the Mn value for the polyalkene from which the substituent groups are derived is 2000, then that substituted succinic acylating agent is characterized by a total of 20 (40,000/2000 = 20) equivalent weights of substituent groups.
In one embodiment the carboxylic acid acylating agent is a substituted succinic acid or anhydride, said substituted succinic acid or anhydride consisting of hydrocarbon-based substituent groups and succinic groups wherein the substituent groups are derived from polybutene in which at least about 50% of the total units derived from butenes is derived from isobutylene. The polybutene is characterized by an Mn value of about 1500 to about 2000 and an Mw/Mn value of about 3 to about 4. These acids or anhydrides are characterized by the presence within their structure of an average of about 1.5 to about 2.5 succinic groups for each equivalent weight of substituent groups.

CA 022130~0 1997-08-1~

In one embodiment the carboxylic acid is at least one substituted succinic acid or anhydride, said substituted succinic acid or anhydride consisting of substituent groups and succinic groups wherein the substituent groups are derived from polybutene in which at least about 50%
of the total units derived from butenes is derived from isobutylene. The polybutene has an Mn value of about 800 to about 1200 and an Mw/Mn value of about 2 to about 3. The acids or anhydrides are characterized by the presence within their structure of an average of about 0.9 to about 1.2 succinic groups for each equiva~ent weight of substituent groups.
The amino compound is characterized by the presence within its structure of at least one HN< group and can be a monoamine or poiyamine. Mixtures of two or more amino compounds can be used in the reaction with one or more acylating reagents. In one embodiment, the amino compound contains at least one primary amino group (i.e., -NH2) and more preferably the amine is a polyamine, especially a polyamine containing at least two -NH- groups, either or both of which are primary or secondary amines. The amines may be aliphatic, cycloaliphatic, aromatic or heterocyclic amines.
Among the useful amines are the alkylene polyamines, including the polyalkylene polyamines. The alkylene polyamines include those conforming to the formula RN-(U-N)n-R
R R
wherein n is from 1 to about 10; each R is independently a hydrogen atom, a hydrocarbyl group or a hydroxy-substituted or amine-substituted hydrocarbyl group having up to about 30 atoms, or two R groups on different nitrogen atoms can be joined together to form a U group, with the proviso that at least one R group is a hydrogen atom and U is an alkylene group of about 2 to about 10 carbon atoms. Preferably, U is ethylene or propylene. Especially preferred are the alkylene polyamines where each R

CA 022130~0 1997-08-1~

is hydrogen or an amino-substituted hydrocarbyl group with the ethylene polyamines and mixtures of ethylene polyamines being the most preferred.
Usually n will have an average value of from about 2 to about 7. Such alkylene polyamines include methylene polyamine, ethylene polyamines, propylene polyamines, butylene polyamines, pentylene polyamines, hexylene polyamines, heptylene polyamines, etc. The higher homologs of such amines and related amino alkyl-substituted piperazines are also included.
Alkylene polyamines that are useful include ethylene diamine, triethylene tetramine, propylene diamine, trimethylene diamine, hexamethylene diamine, decamethylene diamine, octamethylene diamine, di(heptamethylene) l.ia",i"e, tripropylene tel,~,),i,le, tetraethylene pentamine, trimethylene diamine, pentaethylene hexamine, di~trimethylene)triamine, N-(2-aminoethyl)piperazine, 1,4-bis(2-aminoethyl)piperazine, and the like.
Higher homologs as are obtained by condensing two or more of the above-illustrated alkylene amines are useful, as are mixtures of two or more of any of the afore-described polyamines.
Ethylene polyamines, such as those mentioned above, are especially useful for reasons of cost and effectiveness. Such polyamines are described in detail under the heading "Diamines and Higher Amines" in The Encyclopedia of Chemical Technology, Second Edition, Kirk and Othmer, Volume 7, pages 27-39, Interscience Publishers, Division of John Wiley and Sons, 1965, which is hereby incorporated by reference for the disclosure of useful polyamines. Such compounds are prepared most conveniently by the reaction of an alkylene chloride with ammonia or by reaction of an ethylene imine with a ring-opening reagent such as ammonia, etc. These reactions result in the production of the somewhat complex mixtures of alkylene polyamines, including cyclic condensation products such as piperazines.
These mixtures can be used.
Other useful types of polyamine mixtures are those resulting from stripping of the above-described polyamine mi~tures. In this instance, lower molecular weight polyamines and volatile contaminants are removed from an alkylene polyamine mixture to leave as residue what is often termed CA 022130~0 1997-08-1~

-2~
"polyamine bottoms". In general, alkylene polyamine bottoms can be characterized as having less than two, usually less than 1% (by weight) material boiling below about 200~C. In the instance of ethylene polyamine bottoms, which are readily available and found to be quite useful, the bottoms contain less than about 2% (by weight) total diethylene triamine (DETA) or triethylene tetramine (TETAl. A typical sample of such ethylene polyamine bottoms obtained from the Dow Chemical Company of Freeport, Texas designated "E-100" showed a specific gravity at 1 5.6~C of 1.0168, a percent nitrogen by weight of 33.15 and a viscosity at 40~C of 121 centistokes. Gas chromatography analysis of such a sample showed it to contain about 0.93% "Light Ends" Imost probably DETA), 0.72% TETA, 21.74% tetraethylene pentamine and 76.61% pentaethylene hexamine and higher (by weight). These alkylene polyamine bottoms include cyclic condensation products such as piperazine and higher analogs of diethylenetriamine, triethylenetetramine and the like.
These alkylene polyamine bottoms can be reacted solely with the acylating agent, in which case the amino reactant consists essentially of alkylene polyamine bottoms, or they can be used with other amines and polyamines, or alcohols or mixtures thereof. In these latter cases at least one amino reactant comprises alkylene polyamine bottoms.
Other polyamines are described in, for example, U.S. Patents 3,219,666 and 4,234,435, and these patents are hereby incorporated by reference for their disclosures of amines which can be reacted with the acylating agents described above to form the acylated nitrogen-containing compounds (B) of this invention.
In one embodiment, the amine may be a hydroxyamine.
Typically, the hydroxyamines are primary, secondary or tertiary alkanol amines or mixtures thereof. Such amines can be represented by the formulae:

H2N-R'-OH RN(H)-R'-OH RRN-R'-OH

CA 022130~0 1997-08-1~

.

wherein each R is independently a hydrocarbyl group of one to about eight carbon atoms or hydroxyhydrocarbyl group of two to about eight carbon atoms, preferably one to about four, and R' is a divalent hydrocarbyl group of about two to about 18 carbon atoms, preferably two to about four. The group -R '-OH in such formulae represents the hydroxyhydrocarbyl group. R' can be an acyclic, alicyclic or aromatic group. Typically, R' is an acyclic straight or branched alkylene group such as an ethylene, 1 ,2-propylene, 1,2-butylene, 1 ,2-octadecylene, etc. group. Where two R groups are present in the same molecule they can be joined by a direct carbon-to-carbon bond or through a heteroatom le.g., oxygen, nitrogen or sulfur) to form a 5-, 6-, 7-or 8-membered ring structure. Examples of such heterocyclic amines include N-(hydroxyl lower alkyl)-morpholines, -thiomorpholines, -piperidines, -oxazolidines, -thiazolidines and the like. Typically, however, each R', is independently a methyl, ethyl, propyl, butyl, pentyl or hexyl group.
Examples of these alkanolamines include mono-, di-, and triethanol amine, diethylethanolamine, ethylethanolamine, butyldiethanolamine, etc.
The hydroxyamines can also be an ether N-(hydroxyhydrocarbyl)-amine. These are hydroxypoly(hydrocarbyloxy) analogs of the above-described hydroxy amines (these analogs also include hydroxyl-substituted oxyalkylene analogs). Such N-(hydroxyhydrocarbyl) amines can be conveniently prepared by reaction of epoxides with afore-described amines and can be represented by the formulae:

N2N-(R o)x~H RN(H)-(R'O)XH RRN-(R'O)XH
wherein x is a number from about 2 to about 15 and R and R' are as described above. R may also be a hydroxypoly(hydrocarbyloxy) group.
The acylated nitrogen-containing compounds (B) include amine salts, amides, imides, amidines, amidic acids, amidic salts and imidazolines as well as mixtures thereof. To prepare the acylated nitrogen-containing compounds from the acylating reagents and the amino compounds, one or CA 022130~0 1997-08-1~

more acylating reagents and one or more amino compounds are heated, optionally in the presence of a normally liquid, substantially inert organic liquid solventtdiluent, at temperatures in the range of about 80~C up to the decomposition point of either the reactants or the carboxylic derivative but normally at temperatures in the range of about 100~C up to about 300~C
provided 300~C does not exceed the decomposition point. Temperatures of about 125~C to about 250~C are normally used. The acylating reagent and the amino compound are reacted in amounts sufficient to provide from about one-half equivalent up to about 2 moles of amino compound per equivalent of acylating reagent.
Many patents have described useful acylated nitrogen-containing compounds including U.S. Patents 3,172,892; 3,219,666;
3,272,746; 3,310,492; 3,341,542; 3,444,170; 3,455,831; 3,455,832;~
3,576,743; 3,630,904; 3,632,511; 3,804,763; and 4,234,435. A typical acylated nitrogen-containing compound of this class is that made by reacting a poly(isobutene)-substituted succinic acid acylating agent ~e.g., anhydride, acid, ester, etc.) wherein the poly(isobutene) substituent has between about 50 to about 400 carbon atoms with a mixture of ethylenepolyamines having about 3 to about 7 amino nitrogen atoms per ethylenepolyamine and about 1 to about 6 ethylene units made from condensation of ammonia with ethylene chloride. The above-noted U.S. patents are hereby incorporated by reference for their disclosure of acylated amino compounds and their method of preparation.
Another type of acylated nitrogen compound belonging to this class is that made by reacting a carboxylic acid acylating agent with a polyamine, wherein the polyamine is the product made by condensing a hydroxy material with an amine. These compounds are described in U.S.
Patent 5,053,152 which is incorporated herein by reference for its disclosure of such compounds.
Another type of acylated nitrogen compound belonging to this class is that made by reacting the afore-described alkyleneamines with the afore-described substituted succinic acids or anhydrides and aliphatic CA 022130~0 1997-08-1~

monocarboxylic acids having from 2 to about 22 carbon atoms. In these types of acylated nitrogen compounds, the mole ratio of succinic acid to monocarboxylic acid ran~es from about 1 :0.1 to about 1: 1. Typical of the monocarboxylic acid are formic acid, acetic acid, dodecanoic acid, butanoic acid, oleic acid, stearic acid, the commercial mixture of stearic acid isomers known as isostearic acid, tall oil acid, etc. Such materials are more fully described in U.S. Patents 3,216,936 and 3,260,715 which are hereby incorporated by reference for their disclosures in this regard.
Still another type of acylated nitrogen compound useful in making the compositions of this invention is the product of the reaction of a fatty monocarboxylic acid of about 12-30 carbon atoms and the afore-des-cribed alkyleneamines, typically, ethylene-, propylene- or trimethylenepolyamines containing 2 to 8 amino groups and mixtures thereof. The fatty monocarboxylic acids are generally mixtures of straight and branched chain fatty carboxylic acids containing 12-30 carbon atoms.
A widely used type of acylated nitrogen compound is made by reacting the afore-described alkylenepolyamines with a mixture of fatty acids having from 5 to about 30 mole percent straight chain acid and about 70 to about 95%
mole branched chain fatty acids. Among the commercially available mixtures are those known widely in the trade as isostearic acid. These mixtures are produced as a by-product from the dimerization of unsaturated fatty acids as described in U.S. Patents 2,812,342 and 3,260,671.
The branched chain fatty acids can also include those in which the branch is not alkyl in nature, such as found in phenyl and cyclohexyl stearic acid and the chloro-stearic acids. Branched chain fatty carboxylic acidlalkylene polyamine products have been described extensively in the art.
See for example, U.S. Patents 3,110,673; 3,251,853; 3,326,801;
3,337,459; 3,405,064; 3,429,674; 3,468,639; 3,857,791. These patents are hereby incorporated by reference for their disclosure of fatty ac-id/polyamine condensates for use in lubricating oil formulations.

- -CA 022130~0 1997-08-1~

The following specific examples illustrate the preparation of exemplary acylated nitrogen-containing compounds (B) useful with this invention.
ExamDle B-1 1000 parts by weight of polyisobutylene (Mn = 1700) substituted succinic anhydride and 1270 parts by weight of diluent oil are blended together and heated to 110 - C. 59.7 parts by weight of a mixture of polyethyleneamine bottoms and diethylenetriamine are added over a two-hour period. The mixture exotherms to 121 -132 ~ C. The mixture is heated to 149~C with nitrogen blowing. The mixture is maintained at 149-154~C
for one hour with nitrogen blowing. The mixture is then filtered at 149 ~ C.
Diluent oil is added to provide a mixture having an oil content of 55% by weight.
Examr~le B-2 A blend of 800 parts by weight of polyisobutylene (Mn = 940) substituted succinic anhydride and 200 parts by weight of diluent oil is heated to 150 ~ C with a nitrogen sparge. 87.2 parts by weight of methylpentaerythritol are added over a one-hour period while maintaining the temperature at 150-160~C. The mixture is heated to 204~C over a period of eight hours, and maintained at 204-210~ C for six hours. 15.2 parts by weight of a mixture of polyethyleneamine bottoms and diethylenetriamine are added over a one-hour period while maintaining the temperature of the mixture at 204-210~C. 519.5 parts of diluent oil are added to the mixture while maintaining the temperature at a minimum of 177~C. The mixture is cooled to 130~C and filtered to provide the desired product.
(C) PhosPhorus Comr~ound.
The phosphorus compound (C) can be a phosphorus acid, ester or derivative thereof. These include phosphorus acid, phosphorus acid ester, phosphorus acid salt, or derivative thereof. The phosphorus acids include the phosphoric, phosphonic, phosphinic and thiophosphoric acids including dithiophosphoric acid as well as the monothiophosphoric, thiophosphinic and thiophosphonic acids.

CA 022130~0 1997-08-1~

The phosphorus compound (C) can be a phosphorus acid ester derived from a phosphorus acid or anhydride and an alcohol of 1 to about 50 carbon atoms, and in one embodiment 1 to about 30 carbon atoms. It can be a phosphite, a monothiophosphate, a dithiophosphate, or a dithiophosphate disulfide. It can also be a metal, amine or ammonium salt of a phosphorus acid or phosphorus acid ester. It can be a phosphorus containing amide or a phosphorus-containing carboxylic ester.
The phosphorus compound can be a phosphate, phosphonate, phosphinate or phosphine oxide; These compounds can be represented by the formula Rl-(O)a R2-(O)b P = X (C-l) R3-(O)C--wherein in Formula (C-l), R~, R2 and R3 are independently hydrogen or hydrocarbyl groups, X is 0 or S, and a, b and c are independently zero or 1.
The phosphorus compound can be a phosphite, phosphonite, phosphinite or phosphine. These compounds can be represented by the formula Rl-(O)a R2-(O)b ~ P (C-ll) R3-(O)C

wherein in Formula (C-ll), R~, R2 and R3 are independently hydrogen or hydrocarbyl groups, and a, b and c are independently zero or 1.
The total number of carbon atoms in R', R2 and R3 in each of the above Formulae (C-l) and (C-ll) must be sufficient to render the compound soluble in the low-viscosity oil used in formulating the inventive compositions. Generally, the total number of carbon atoms in R', R2 and R3 is at least about 8, and in one embodiment at least about 12, and in one embodiment at least about 16. There is no limit to the total number of CA 022130~0 1997-08-1~

carbon atoms in R', R2 and R3 that is reguired, but a practical upper limit is about 400 or about 500 carbon atoms. In one embodiment, R1, R2 and R3 in each of the above formulae are independently hydrocarbyl groups of 1 to about 100 carbon atoms, or 1 to about 50 carbon atoms, or 1 to about 30 carbon atoms, with the proviso that the total number of carbons is at least about 8. Each R1, R2 and R3 can be the same as the other, although they may be different. Examples of useful R1, R2 and R3 groups include isopropyl, n-butyl, isobutyl, amyl, 4-methyl-2-pentyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, alkylnaph-thyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl, alkylnaphthylalkyl, and the like.
The phosphorus compounds represented by Formulae (C-l) and (C-ll) can be prepared by reacting a phosphorus acid or anhydride with an alcohol or mixture of alcohols corresponding to R1, R2 and R3 in Formulae (C-l) and IC-II). The phosphorus acid or anhydride is generally an inorganic phosphorus reagent such as phosphorus pentoxide, phosphorus trioxide, phosphorus tetraoxide, phosphorus acid, phosphorus halide, or lower phosphorus esters, and the like. Lower phosphorus acid esters contain from 1 to about 7 carbon atoms in each ester group. The phosphorus acid ester may be a mono, di- or triphosphoric acid ester.
The phosphorus compound (C) can be a compound represented by the formula R'(X1)a X3 (C-lll) ~ 11 R2(X2)b wherein in Formula (C-lll): Xl, X2, X3 and X4 are independently oxygen or sulfur, and X1 and X2 can be NR4; a and b are independently zero or one; R', R2 R3 and R4 are independently hydrocarbyl groups, and R3 and R4 can be hydrogen.

CA 022130~0 1997-08-1~

Useful phosphorus compounds of the type represented by Formula (C-Ill) are phosphorus- and sulfur-containing compounds. These include those compounds wherein at least one X3 or X4 iS sulfur, and in one embodiment both X3 and X4 are sulfur, at least one X' or X2 is oxygen or sulfur, and in one embodiment both X' and X2 are oxygen, a and b are each 1, and R3 is hydrogen. Mixtures of these compounds may be employed in accordance with this invention.
In Formula (C-lll), R~ and R2 are independently hydrocarbyl groups that are preferably free from acety~enic unsaturation and usually also from ethylenic unsaturation and in one embodiment have from about 1 to about 50 carbon atoms, and in one embodiment from about 1 to about 30 carbon atoms, and in one embodiment from about 1 to about 18 carbon atoms, and in one embodiment from about 1 to about 8 carbon atoms. Each R' and R2 can be the same as the other, although they may be different and either or both may be mixtures. Examples of R1 and R2 groups include isopropyl, n-butyl, isobutyl, amyl, 4-methyl-2-pentyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, alkylnaph-thyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl, alkylnaphthylalkyl, and mixtures thereof. Particular examples of useful mixtures include, for example, isopropyl/n-butyl; isopropyl/secondarybutyl; isopropyl/4-methyl-2-pentyl; isopropyl/2-ethyl-1 -hexyl; isopropyl/isooctyl; isopropyl/decyl; isopro-pyl/dodecyl; and isopropyl/tridecyl.
In Formula (C-lll), R3 and R4 are independently hydrogen or hydrocarbyl groups (e.g. alkyl) of 1 to about 12 carbon atoms, and in one embodiment 1 to about 4 carbon atoms. R3 is preferably hydrogen.
Phosphorus compounds corresponding to Formula ~C-III) wherein X3 and X4 are sulfur can be obtained by the reaction of phosphorus pentasulfide (P2S5) and an alcohol or mixture of alcohols corresponding to R' and R2. The reaction involves mixing at a temperature of about 20~C to about 200~C, four moles of alcohol with one mole of phosphorus pentasulfide. Hydrogen sulfide is liberated in this reaction. The oxygen-containing analogs of these CA 022130~0 1997-08-1~

compounds can be prepared by treating the dithioic acid with water or steam which, in effect, replaces one or both of the sulfur atoms.
In one embodiment, the phosphorus compound (C) is a monothio-phosphoric acid ester or a monothiophosphate. Monothiophosphates are prepared by the reaction of a sulfur source and a dihydrocarbyl phosphite.
The sulfur source may be elemental sulfur, a sulfide, such as a sulfur coupled olefin or a sulfur coupled dithiophosphate. Elemental sulfur is a useful sulfur source. The preparation of monothiophosphates is disclosed in U.S. Patent 4,755,311 and PCT Publication W0 87/07638 which are 1 0 incorporated herein by reference for their disclosure of monothiophosphates, sulfur sources for preparing monothiophosphates and the process for making monothiophosphates.
Monothiophosphates may also be formed in the lubricant blend or functional fluid by adding a dihydrocarbyl phosphite to a lubricating oil 1~ composition or functional fluid containing a sulfur source. The phosphite may react with thè sulfur source under blending conditions (i.e., tempera-tures from about 30~C to about 100~C or higher) to form the monothio-phosphate.
Useful phosphorus acid esters include those prepared by reacting a phosphoric acid or anhydride with cresol alcohols. An example is tricresol phosphate.
In one embodiment, the phosphorus compound (C) is a dithiophos-phoric acid or phosphorodithioic acid. The dithiophosphoric acid can be reacted with an epoxide or a glycol to form an intermediate. The 2~ intermediate is then reacted with a phosphorus acid, anhydride, or lower ester. The epoxide is generally an aliphatic epoxide or a styrene oxide.
Examples of useful epoxides include ethylene oxide, propylene oxide, butene oxide, octene oxide, dodecene oxide, styrene oxide, etc. Propylene oxide is useful. The glycols may be aliphatic glycols having from 1 to about ~ 2, and in one embodiment about ~ to about 6, and in one embodiment 2 or 3 carbon atoms, or aromatic glycols. Aliphatic glycols include ethylene glycol, propylene glycol, triethylene glycol and the like. Aromatic glycols include CA 022130~0 1997-08-1~

hydroquinone, catechol, resorcinol, and the like. These are described in U.S.
patent 3,1 97,405 which is incorporated herein by reference for its disclosure of dithiophosphoric acids, glycols, epoxides, inorganic phosphorus reagents and methods of reacting the same.
In one embodiment the phosphorus compound (C) is a phosphite. The phosphite can be a di- or trihydrocarbyl phosphite. Each hydrocarbyl group can have from 1 to about 24 carbon atoms, or from 1 to about 18 carbon atoms, or from about 2 to about 8 carbon atoms. Each hydrocarbyl group may be independently alkyl, alkehyl or aryl. When the hydrocarbyl group is an aryl group, then it contains at least about 6 carbon atoms; and in one embodiment about 6 to about 18 carbon atoms. Examples of the alkyl or alkenyl groups include propyl, butyl, hexyl, heptyl, octyl, oleyl, linoleyl, stearyl, etc. Examples of aryl groups include phenyl, naphthyl, heptylphenol, etc. In one embodiment each hydrocarbyl group is independently propyl, butyl, pentyl, hexyl, heptyl, oleyl or phenyl, more preferably butyl, oleyl or phenyl and more preferably butyl or oleyl. Phosphites and their preparation are known and many phosphites are available commercially. Useful phosphites include dibutyl hydrogen phosphite, trioleyl phosphite and triphenyl phosphite.
In one embodiment, the phosphorus compound (C) is a phosphorus-containing amide. The phosphorus-containing amides may be prepared by the reaction of a phosphorus acid (e.g., a dithiophosphoric acid as described above) with an unsaturated amide. Examples of unsaturated amides include acrylamide, N,N'-methylenebisacrylamide, methacrylamide, crotonamide, and the like. The reaction product of the phosphorus acid with the unsaturated amide may be further reacted with linking or coupling compounds, such as formaldehyde or paraformaldehyde to form coupled compounds. The phosphorus-containing amides are known in the art and are disclosed in U.S.
Patents 4,876,374, 4,770,807 and 4,670,169 which are incorporated by reference for their disclosures of phosphorus amides and their preparation.
In one embodiment, the phosphorus compound (C) is a phosphorus-containing carboxylic ester. The phosphorus-containing carboxylic esters CA 022130~0 1997-08-1~

may be prepared by reaction of one of the above-described phosphorus acids, such as a dithiophosphoric acid, and an unsaturated carboxylic acid or ester, such as acrylic acid or a vinyl or allyl carboxylic acid or ester. If the carboxylic acid is used, the ester may then be formed by subsequent reac-tion with an alcohol.
The vinyl ester of a carboxylic acid may be represented by the formula RCH=CH-O(O)CR1 wherein R is a hydrogen or hydrocarbyl group having from 1 to about 30 carbon atoms, preferably hydrogen or a hydrocarbyl group having 1 to about 12,~more preferably hydrogen, and R1 is a hydrocarbyl group having 1 to about 30 carbon atoms, preferably 1 to about 12, more preferably 1 to about 8. Examples of vinyl esters include vinyl acetate, vinyl 2-ethylhexanoate, vinyl butanoate, and vinyl crotonate.
In one embodiment, the unsaturated carboxylic ester is an ester of an unsaturated carboxylic acid, such as maleic, fumaric, acrylic, methacrylic, itaconic, citraconic acids and the like. The ester can be represented by the formula RO-(O)C-HC = CH-C(O)OR wherein each R is independently a hydrocarbyl group having 1 to about 18 carbon atoms, or 1 to about 12, or 1 to about 8 carbon atoms. Examples of unsaturated carboxylic esters that are useful include methylacrylate, ethylacrylate, 2-ethylhexylacrylate, 2-hydroxyethylacrylate, ethylmethacrylate, 2-hydroxyethylmethacrylate, 2-hydroxypropylmethacrylate, 2-hydroxypropylacrylate, ethylmaleate, butylmaleate and 2-ethylhexylmaleate. The above list includes mono- as well as diesters of maleic, fumaric and citraconic acids.
In one embodiment, the phosphorus compound (C) is the reaction product of a phosphorus acid and a vinyl ether. The vinyl ether is represent-ed by the formula R-CH2'CH-OR1 wherein R is hydrogen or a hydrocarbyl group having 1 to about 30, preferably 1 to about 24, more preferably 1 to about 12 carbon atoms, and Rl is a hydrocarbyl group having 1 to about 30 carbon atoms, preferably 1 to about 24, more preferably 1 to about 12 CA 022130~0 1997-08-1~

carbon atoms. Examples of vinyl ethers include vinyl methylether, vinyl propylether, vinyl 2-ethylhexylether and the like.
When the phosphorus compound (C) is acidic, it may be reacted with an ammonia or a source of ammonia, an amine, or metallic base to form the corresponding salt. The salts may be formed separately and then added to the lubricating oil or functional fluid composition. Alternatively, the salts may be formed when the acidic phosphorus compound (C) is blended with other components to form the lubricating oil or functional fluid composition.
The phosphorus compound can then form salts with basic materials which are in the lubricating oil or functional fluid composition such as basic nitrogen containing compounds (e.g., the above-discussed acylated nitrogen-containing compounds (8)) and overbased materials.
The metal salts which are useful with this invention include those salts containing Group IA, IIA or IIB metals, aluminum, lead, tin, iron, molybdenum, manganese, cobalt, nickel or bismuth. Zinc is an especially useful metal. These salts can be neutral salts or basic salts. Examples of useful metal salts of phosphorus-containing acids, and methods for preparing such salts are found in the prior art such as U.S. Patents 4,263,150, 4,289,635; 4,308,154; 4,322,479; 4,417,990; and 4,466,895, and th disclosures of these patents are hereby incorporated by reference. These salts include the Group ll metal phosphorodithioates such as zinc dicyclohex-ylphosphorodithioate, zinc dioctylphosphorodithioate, barium di(heptylphen-yl)-phosphorodithioate, cadmium dinonylphosphorodithioate, and the zinc salt of a phosphorodithioic acid produced by the reaction of phosphorus pentasulfide with an equimolar mixture of isopropyl alcohol and n-hexyl alcohol.
The following examples illustrate the preparation of useful metal salts of the phosphorus compounds (C).

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ExamPle C-1 (a) A mixture of 317.33 grams (5.28 moles) of 2-propanol and 359.67 grams (3.52 moles) of 4-methyl-2-pentanol is prepared and heated to 60~C. Phosphorus pentasulfide (444.54 grams, 2.0 moles) is added to the alcohol mixture while maintaining the temperature at 60 ~ C. Two moles of hydrogen sulfide are liberated and trapped with a 50% aqueous sodium hydroxide trap. The mixture is heated to and maintained at 70~C for two hours. The mixture is cooled to room temperature and filtered through diatomaceous earth to yield a liquid green product having an acid number in the range of 193-203.
(b) 89.1 grams (1.1 mo!es) of ZnO are added to 200 ml of toluene.
566.6 grams (2.0 equivalents based on acid number) of the product from part (a) are added dropwise to the ZnO/toluene mixture. The resulting reaction is exothermic. The reaction mixture is stripped to 70 ~ C and 20 mm Hg to remove water of reaction, toluene and excess aicohol. The residue is filtered through diatomaceous earth. The filtrate, which is the desired product, is a yellow viscous liquid.
Examr le C-2 137.6 grams of zinc oxide are mixed with 149.9 grams of diluent oil.
17.7 grams of 2-ethylhexanoic acid are added. 1000 grams of a phosphorodithioic acid derived from P2S5 and 2-ethylhexanol are then added to the mixture. The mixture is allowed to neutralize. It is then flash dried and vacuum stripped. 81.1 grams of triphenyl phosphite are added. The temperature of the mixture is adjusted to 124-129~C and maintained at that temperature for three hours. The mixture is cooled to room temperature and filtered using filter aid to provide the desired product.
When the phosphorus compound (C) is an ammonium salt, the salt is considered as being derived from ammonia (NH3) or an ammonia yielding compound such as NH40H. Other ammonia yielding compounds will readily occur to those skilled in the art.

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When the phosphorus compound (C) is an amine salt, the salt may be considered as being derived from amines. Any of the amines discussed above under the subtitle"(B) Acylated Nitrogen-Containing Compoundsn can be used.
The following examples illustrate the preparation of amine or ammonium salts of the phosphorus compounds (C) that can be used with this invention.
ExamDle C-3 Phosphorus pentoxide (2û8 grams, 1.41 moles) is added at 50- C to 60~C to hydroxypropyl 0,0'-diisobutylphosphorodithioate (prepared by reacting 280 grams of propylene oxide with 11 84 grams of O,0'-di-isobutylphosphorodithioic acid at 30~C to 60~C). The reaction mixture is heated to 80~C and held at that temperature for 2 hours. To the acidic reaction mixture there is added a stoichiometrically equivalent amount (384 grams) of a commercial aliphatic primary amine at 30~C to 60~C. The product is filtered. The filtrate has a phosphorus content of 9.31%, a sulfur content of 11.37%, a nitrogen content of 2.50%, and a base number of 6.9 (bromphenol blue indicator).
Examnle C-4 (a) 0,O-di-(2-ethylhexyl) dithiophosphoric acid (354 grams) having an acid number of 154 is introduced into a stainless steel "shaker" type autoclave of 1320 ml capacity having a thermostatically controlled heating jacket. Propylene oxide is admitted until the pressure rises to 170 psig at room temperature, and then the autoclave is sealed and shaken for 4 hours at 50~C to 100~C during which time the pressure rises to a maximum of 550 psig. The pressure decreases as the reaction proceeds. The autoclave is cooled to room temperature, the excess propylene oxide is vented and the contents removed. The product (358 grams), a dark liquid having an acid number of 13.4, is substantially 0,0-di-(2-ethylhexyl)-S-hydroxyisopropyl dithiophosphate.

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(b) Ammonia is blown into the product of part ~a) until a substantially neutral product is obtained.
The phosphorus compound (C) can be a phosphorus-containing sulfide represented by the formula R1O-P-S-(S)n-P-OR3 (C-IV) R2O/ \OR4 wherein in Formula (C-IV), R1, R2, R3 and R4 are independently hydrocarbyl groups, Xl and X2 are independently O or S, and n is zero to 3. In one embodiment Xl and X2 are each S, and n is 1. Rl, R2, R3 and R4 are indepen-dently hydrocarbyl groups that are preferably free from acetylenic unsatura-tion and usually also free from ethylenic unsaturation. In one embodiment R1, R2, R3 and R4 independently have from about 1 to about 50 carbon 1 5 atoms, and in one embodiment from about 1 to about 30 carbon atoms, and in one embodiment from about 1 to about 18 carbon atoms, and in one embodiment from about 1 to about 8 carbon atoms. Each Rl, R2, R3 and R4 can be the same as the other, although they may be different and mixtures may be used. Examples of Rl, R2, R3 and R4 groups include isopropyl, butyl, n-butyl, isobutyl, amyl, 4-methyl-2-pentyl, octyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, alkylnaph-thyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl, alkylnaphthylalkyl, and mixtures thereof.
The compounds represented by Formula (C-IV) can be prepared by first reacting an alcohol, phenol or aliphatic or aromatic mercaptan with a sulfide of phosphorus, such as P2S3, P2S6, P4S3, P4S7, P4Slo, and the like, to form a partially esterified thiophosphorus or thiophosphoric acid, and then further reacting this product as such or in the form of a metal salt with an oxidizing agent or with a sulfur halide. Thus, when an alcohol is reacted CA 022130~0 1997-08-1~

with phosphorus trisulfide, a dialkylated monothiophosphorus acid is formed according to the following equation:
4ROH + P2S3~ 2(RO)2PSH + H2S
This alkylated thiophosphorus acid may then be treated with an oxidizing agent such as hydrogen peroxide or with sulfur dichloride or sulfur monochloride to form a disulfide, trisulfide, or tetrasulfide, respectively, according to the following equations:
4(RO)2PSH + ~2 2~RO)2P-S-S-P(OR)2 + 2H2~
2(RO)2PSH + SC12 ~ (RO)2P-S-S-S-P(OR)2 + 2HCI
2(RO)2PSH + S2C12 (RO)2p-s-(s)2-s-p-(oR)2 + 2HCI
Similarly, when the alcohol is reacted with phosphorus pentasulfide, the corresponding di-substituted dithiophosphoric acid is formed, and this may likewise be converted into disulfide, trisulfide or tetrasulfide compounds.
Suitable alcohols such as those discussed below may be employed.
Sulfurized alcohols such as sulfurized oleyl alcohol may also be used.
Corresponding reactions take place by starting with mercaptans, phenols or thiophenols instead of alcohols. Suitable oxidizing agents for converting the thiophosphorus and thiophosphoric acids to disulfides include iodine, potassium triodide, ferric chloride, sodium hypochlorite, hydrogen peroxide, oxygen, etc.
Alcohols that can be used to prepare the phosphorus-containing sulfides of Formula (C-IVJ include the alcohols discussed above under the subtitle "(A) Thiocarbonates".
The following examples illustrate the preparation of phosphorus-containing sulfides (C) represented by Formula (C-IV) that are useful with this invention.
ExamDle C-5 A phosphorodithioic acid derived from P2S6 and an alcohol mixture of 40% by weight isopropyl alcohol and 60% by weight 4-methyl-secondary-amyl alcohol (4518 grams, 14.34 equivalentst is charged to a CA 022130~0 1997-08-1~

reactor. A 30% aqueous hydrogen peroxide solution (1130 grams, 10.0 moles) is added dropwise at a rate of 7.3 grams per minute. The temperature of the reaction mixture increases from 24~C to 38~C. A 50%
aqueous sodium hydroxide solution (40 grams, 0.50 equivalents) is added.
The reaction mixture is stirred for 5 minutes, and then allowed to stand.
The mixture separates into two layers. The aqueous layer contains water, phosphorodithioic acid salt and excess alcohol from the phosphorodithioic acid. The organic layer contains the desired product. The aqueous layer is drawn off (1108 grams) and thb remaining organic portion is stripped at 100~C and 20 mm Hg for two hours. The stripped organic product is filtered using a filter aid to provide the desired product which is a phosphorus-containing disulfide in the form of a clear yellow liquid (4060 grams).
ExamDle C-6 A phosphorodithioic acid derived from 4-methyl-2-pentanol and P2S5 (1202 grams, 3.29 equivalents) is charged to a reactor. A 30%
aqueous hydrogen peroxide solution (319 grams, 2.82 moles) is added dropwise at a rate of 7.3 grams per minute. The temperature of the reaction mixture increases from 24~C to 38~C. A 50% aqueous sodium hydroxide solution (12 grams, 0.15 equivalents) is added. The reaction mixture is stirred for 5 minutes, and then allowed to stand. The mixture separates into two layers. The aqueous layer contains water, phosphorodithioic acid salt and excess methylamyl alcohol from the phosphorodithioic acid. The organic layer contains the desired product. The aqueous layer is drawn off and the remaining organic portion is stripped at 100~C and 20 mm Hg for two hours.
The stripped organic product is filtered using filter aid to provide the desiredphosphorus-containing disulfide product which is a clear yellow liquid (1016 grams).

-CA 022130~0 1997-08-1~

ExamPle C-7 (a) A m;xture of 105.6 grams (1.76 moles) of isoProPYl alcohol and 269.3 grams (2.64 moles) of 4-methyl-2-pentanol is prepared and heated to 70~ C. Phosphorus pentasulfide (222 grams, 1 mole) is added to the alcohol mixture while maintaining the temperature at 70 ~ C. One mole of hydrogen sulfide is liberated. The mixture is maintained at 70~C for an additional four hours. The mixture is filtered through diatomaceous earth to yield a green liquid product having an acid number in the range of 179-189.
(b) 44.6 grams (1.09 equivalents) of ZnO are added to diluent oil to form a slurry. One equivalent (based upon the measured acid number) of the phosphorodithioic acid prepared in (a) are added dropwise to the ZnO slurry. The reaction is exothermic. The reaction mixture is stripped to 100~ C and 20 mm Hg to remove water of reaction and excess alcohol.
The residue is filtered through diatomaceous earth. The filtrate, which is a viscous liquid, is diluted with diluent oil to provide a final product having a 9.5% by weight phosphorus content.
(c) A mixture of the product of part (a) of this example ( 184 grams) and part (b) (130 grams) is placed in a reactor. A 30% aqueous hydrogen peroxide solution (80 grams) is added dropwise. After the hydrogen peroxide addition is complete, the reaction mixture is stripped at 70~C and 20 mm Hg. The reaction mixture is filtered through diatomaceous earth to provide the desired product which is in the form of a yellow liquid.
(D) Organic Sulfide.
The organic sulfides (D) that are useful with this invention are compounds represented by the formula X' X2 Tl-C-S-(S)n-C-T2 (D-l) CA 022130~0 1997-08-1~

wherein in Formula (D-l), T1 and T2 are independently R, OR, SR or NRR
wherein each R is independently a hydrocarbyl group, X1 and X2 are independently O or S, and n is zero to 3. In one embodiment, X' and X2 are each S. In one embodiment, n is 1 to 3, and in one embodiment, n is 1.
Thus, compounds represented by the formula Il 11 T1-C-S-S-C-T2 (D-ll) wherein in Formula (D-ll), T' and T2 are as defined above can be used. In one embodiment, each R is a hydrocarbyl group of 1 to about 50 carbon atoms, and in one embodiment 1 to about 40 carbon atoms, and in one embodiment 1 to about 30 carbon atoms, and in one embodiment 1 to about 20 carbon atoms. In one embodiment, each R is independently methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, amyl, ~methyl-2-pentyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, alkylnaphthyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl or alkylnaphthylalkyl.
In one embodiment, the organic sulfide is a compound represented by the formula:

O O
Il 11 R-C-S-(S)n-C-R (D-lll) wherein in Formula (D-lll), R and n are as defined above, with compounds wherein n is 1 being especially useful.
In one embodiment, the organic sulfide is a compound represented by the formula - - -CA 022130~0 1997-08-1~

S S
Il 11 RO-C-S-(S)n-C-OR (D-IV) wherein in Formula ID-IV), R and n are as defined above, with compounds wherein n is 1 being useful.
In one embodiment, the organic sulfide is a compound represented by the formula Il 11 RS-C-S-(S)n-C-SR (D-V) wherein in Formula (D-V), R and n are as defined above, with compounds wherein n is 1 being especially useful.
In one embodiment, the organic sulfide is a compound represented by the formula S S
Il 11 RRN-C-S-(S)n-C-NRR (D-VI) wherein in Formula (D-VI), R and n are as defined above, with compounds wherein n is 1 being especially useful.
These compounds are known and can be prepared by conventional techniques. For example, an appropriate mercaptan, alcohol or amine can first be reacted with an alkali metal reagent (e.g., NaOH, KOH) and carbon disulfide to form the corresponding thiocarbonate or dithiocarbamate. The thiocarbonate or dithiocarbamate is then reacted with an oxidizing agent (e.g., hydrogen peroxide, cobalt maleonitriledithioate, K2Fe(CN)6, FeCI3, dimethylsulfoxide, dithiobis(thioformate), copper sulfate, etc.) to form a disulfide, or with sulfur dichloride or sulfur monochloride to -CA 022130~0 1997-08-1~

form a trisulfide or tetrasulfide, respectively. The oxygen-containing analogs of these compounds wherein X1 and X2 in Formula (D-l) are oxygen can be prepared by treating the sulfur-containing compounds with water or steam.
Alcohols used to prepare the organic sulfides of Formula (D-l) can be any of those described above under the subtitle "(C) Phosphorus CompoundN.
The amines that can be used include those described above under the subtitle "(B) Acylated Nitrogen-Containing Compounds".
Mercaptans that can be used include those described above under the subtitle ~(A) ThiocarbonatesN.
The following examples illustrate the preparation of organic sulfides (D) that are useful with this invention.
ExamPle D-1 Di-n-butylamine (129 grams, 1 equivalent) is charged to a 1 5 reactor. Carbon disulfide (84.0 grams, 1.1 equivalents) is added dropwise over a period of 2.5 hours. The resulting reaction is exothermic but the temperature of the reaction mixture is maintained below 50~C using an ice bath. After the addition of carbon disulfide is complete the mixture is maintained at room temperature for one hour with stirring. A 50% aqueous sodium hydroxide solution (80 grams) is added and the resulting mixture is stirred for one hour. A 30% aqueous hydrogen peroxide solution (200 grams) is added dropwise. The resulting reaction is exothermic but the temperature of the reaction mixture is maintained below 50~C using an ice bath. The mixture is transferred to a separatory funnel. Toluene (800 2~ grams) is added to the mixture. The organic layer is separated from the product and washed with one liter of distilled water. The separated and washed organic layer is dried over sodium carbonate and filtered through diatomaceous earth. The mixture is stripped on a rotary evaporator at 77~C
and 20 mm Hg to provide the desired dithiocarbamate disulfide product which is in the form of a dark orange liquid.

-CA 022130~0 1997-08-1~

.

ExamPle D-2 Di-n-butyl amine (1350 grams) is charged to a reactor. Carbon disulfide ~875 grams) is added dropwise while maintaining the mixture below 50-C. A 50% aqueous sodium hydroxide solution (838 grams) is added dropwise. A 30% aqueous H2O2 solution (2094 grams) is added dropwise.
The reaction mixture exotherms. An aqueous layer and an organic layer form. The aqueous layer is separated from the organic layer. Diethyl ether (1000 grams) is mixed with the aqueous layer to extract organic material from it. The diethyl ether containing extract is added to the organic layer.
The resulting mixture is stripped at 70~ C and 20 mm Hg, and then filtered through diatomaceous earth to provide the desired disulfide product which is in the form of a brown liquid.
ExamPle D-3 A mixture of 1-octanethiol (200 grams), 50% aqueous NaOH
solution (110 grams) and toluene (200 grams) is prepared and heated to reflux ( 1 20 ~ C) to remove water. The mixture is cooled to room temperature and carbon disulfide (1 14.5 grams) is added. A 30% aqueous H2O2 solution (103 grams) is added dropwise while maintaining the temperature below 50~C. Diethyl ether is added and then extracted. The organic layer is isolated, washed with distilled water, dried and chromotographed using hexane to provide the desired disulfide product which is in the form of a yellow liquid.
ExamPle D-4 (a) A mixture of 4000 grams of dodecyl mercaptan, 1600 grams of a 50% aqueous NaOH solution and 2000 grams of toluene is prepared and heated to 125~C to remove 1100 grams of water. The reaction mixture is cooled to 40~C and 1672 grams of carbon disulfide are added. The mixture is heated to 70~C and maintained at that temperature for ~ hours. The mixture is filtered using diatomaceous earth and stripped -CA 022130~0 1997-08-1~

at 100 ~C and 20 mm Hg to form the desired product which is in the form of a red liquid.
(b) 200 grams of the product from part (a) and 200 grams of hexane are placed in a reactor and cooled to 10 ~ C. 130 grams of a 30%
aqueous H2O2 solution are added dropwise while maintaining the temperature below 45 - C. The mixture is extracted with diethyl ether. The organic portion is washed with water, dried with Na2CO3, filtered, and heated under azeotropic conditions to remove water and provide the desired disulfide product which is in the form of a bright red liquid.
E~ le D-5 1700 grams of methylpentanol and 407 grams of potassium hydroxide are placed in a reactor. The mixture is heated under reflux conditions to remove 130-135 grams of water. The mixture is cooled to 50~C, and 627 grams of carbon disulfide are added. 750 grams of a 30%
aqueous H2Oz solution are added dropwise. The mixture exotherms, and an aqueous layer and an organic layer are formed. The aqueous layer is separated from the organic layer. The organic layer is stripped at 100 ~ C and 20 mm Hg and filtered to provide the desired disulfide product which is in the form of an orange liquid.
Example D-6 1100 grams of methylpentyi alcohol and 863 grams of a 50%
aqueous NaOH solution are placed in a reactor and heated to 120~C to remove 430 grams of water. The mixture is cooled to 50 ~ C and 925 grams of carbon disulfide are added. 623 grams of a 30% aqueous H2O2 solution are added dropwise. The resulting reaction is exothermic, and an aqueous and an organic layer are formed. The aqueous layer is separated. The organic layer is stripped at 100~ C and 20 mm Hg and filtered to provide the desired disulfide product.

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ExamDle D-7 A mixture of isopropyl alcohol (132 grams), methyl pentyl alcohol (330 grams) and a 50% aqueous NaOH solution (435 grams) is prepared. Water (50 grams) is removed using distillation at 70~C. The mixture is cooled to room temperature and carbon disulfide (4~5 grams) is added. A 30% aqueous H202 solution (1352 grams) is added dropwise while ma;ntaining the temperature below 50~C. Water is removed. The resulting organic layer is stripped at 70~C and ~0 mm Hg to form a paste-like composition. The paste-lilce composition is filtered to provide the desired disulfide product which is in the form of a red liquid.
(E)Heterocvclic Com~ounds The heterocyclic compounds are compounds represented by the formula Xl 1 5 ./1~
X2 X3 (E-l) G' ~ ~ G4 wherein in Formula (E-l): X~, X2 and X3 are independently O or S, and X2 and X3 can be NR1 wherein R1 is hydrogen or hydrocarbyl; and G1, G2, G3 and G4 are independently R2, OR2 or R30R2, wherein R2 is hydrogen or hydrocarbyl and R3 is hydrocarbylene or hydrocarbylidene. In one embodiment, G1 is R2, OR2 or R30R2, and G2, G3 and G4 are each hydrogen. In one embodiment, at least one of X1, X2 or X3 is oxygen. In one embodiment, the heterocyclic compound is a compound represented by one of the following formulas:

CA 022130~0 1997-08-1~

S S S
O~S S J~ SHN ~ S
)J '~J ~
G1 G1 G~
(E-IA) (E-IB) (E-IC) wherein in each of the above formulas, G1 has the same meaning as in Formula (A-l).
In one embodiment, each R1 and R2 is, independently, a hydrocarbyl group of 1 to about 100 carbon atoms, and in one embodiment 1 to about 50 carbon atoms, and in one embodiment 1 to about 40 carbon atoms, and in one embodiment 1 to about 30 carbon atoms, and in one embodiment about 4 to about 20 carbon atoms, and in one embodiment about 8 to about 14 carbon atoms. The hydrocarbyl groups can be unsubstituted or they can be substituted with one or more halo, 1 5 carbonylalkoxy, alkoxy, thioalkyl, thiol, cyano, hydroxyl or nitro groups. The hydrocarbyl groups can be alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, alkaryl or aralkyl. Examples include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, amyl, ~methyl-2-pentyl, 2-ethylhexyl, isooctyl, decyl, dodecyl, tetradecyl, 2-pentenyl, dodecenyl, phenyl, naphthyl, alkylphenyl, Z0 alkylnaphthyl, phenylalkyl, naphthylalkyl, alkylphenylalkyl or alkylnaphthyalkyl .
The hydrocarbylene or hydrocarbylidene groups R3 generally have from 1 to about 20 carbon atoms, and in one embodiment 1 to about 12 carbon atoms, and in one embodiment 1 to about 6 carbon atoms.
These groups can be alkylene, alkylidene, arylene, alkylarylene, arylalkylene, etc. Examples include methylene, ethylene, propylene, butylene, isobutylene, pentylene, hexylene, phenylene, methylphenylene, phenylethylene, etc.

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These compounds can be prepared by reacting CS2, COS, C0z, or a source material for these reactants, with a compound represented by the formula.

C C \ (E-ll) G1 l l G4 wherein in Formula (E-ll), X is 0, S or NR1, and R1, G1, G2, G3 and G4 are the same as in Formula (E-l), in the presence of a catalyst. The reactants represented by the Formula (E-ll) can be epoxides, episulfides or aziridines including 1,2-epoxides, 1,2-episulfides, 1,2-aziridines, internal epoxides, internal episulfides, and internal aziridines.
Examples of useful epoxides include: ethylene oxide; propylene oxide; 1,2-epoxyhexane; 1,2-epoxyhexadecane; 1,2-epoxybutane; 3,4-epoxyheptane; 1,2-epoxy-cyclohexane; 4,5-epoxydecane; 1,2-epoxydodecane; 1,2-epoxytetradecane; 1,2-epoxy-5-oxy-heptane; 1,2-epoxy-6-propyltridecane; oxetanes; 9,10-epoxystearic acid esters; styrene oxides; para-chlorostyrene oxide; and mixtures of two or more of these.
Also included are the epoxidized fatty acid esters. Typical fatty acid esters include C1 20 alkyl esters of C8 24 unsaturated fatty acids such as palmitoleic, oleic, ricinoleic, petroselic, linoleic, linolenic, oleostearic, licanic, etc. Specific examples of the fatty acid esters which can be epoxidized include lauryl tallate, methyl oleate, lauryl oleate, cetyl oleate, cetyl linoleate, lauryl ricinoleate, oleyl linoleate, oleyl stearate and alkyl glycerides. Also useful are the saturated fatty acid esters prepared from mixed unsaturated fatty acid esters such as are obtained from animal fats and vegetable oils including tall oil, linseed oil, olive oil, castor oil, soybean oil, peanut oil, rape seed oil, fish oil, sperm oil, etc.

-CA 022130~0 1997-08-1~ .

Examples of useful episulfides include: 1 ,2-epithiohexane; 4,5-epithiooctane; 1 ,2-epithiodecane, 1 ,2-epithiododecane; 1,2-epithiotetradecane; and the episulfides derived from fatty acid esters (e.g., 9,1 0-epithiostearic acid ester) including the fatty acid esters derived from animal fats and vegetable oils (e.g., tall oil, soybean oil, fish oil, etc.).
Examples of useful aziridines include hexylazacyclopropane, octylazacyclopropane, decylazacyclopropane, dodecylazacyclopropane, tetradecylazacyclopropane, and the aziridines derived from fatty acid esters including the fatty acid esters derived from animal fats and vegetable oils.
Generally, any epoxide, episulfide or aziridine which is stable under the reaction conditions employed may be used, but the reactivity of terminal epoxides, episulfides and aziridines make them especially useful.
The higher molecular weight epoxides, episulfides and aziridines (e.g., Cl0.20 epoxides, episulfides and aziridines) are useful for imparting higher levels of oil solubility to the cyclic organic sulfides.
The catalyst can be an alkali metal halide, alkoxide, alkyl xanthate, or quaternary ammonium salt. The alkali metals are preferably lithium, sodium or potassium, with lithium being especially useful. The halides can be fluoride, chloride, bromide or iodide, with bromide being especially useful. The alkyl portion of the alkoxides and alkyl xanthates generally contain from ~ to about 8 carbon atoms. Examples include methoxide, ethoxide, isopropoxide, t-butoxide, hexoxide, octoxidel methyl xanthate, ethylxanthate, butyl xanthate, hexylxanthate and octyl xanthate.
Lithium bromide and sodium methoxide are useful catalysts. Tetraalkyl ammonium halide salts can be used, with tetrabutyl ammonium bromide being especially useful.
The mole ratio of CS2, COS or C02 to the reactants represented by Formula (E-ll) is generally in the range of about 0.5 to about 10, and in one embodiment about 0.5 to about 5, and in one embodiment about 1 to about 1.2. The weight ratio of CS2, COS or CO2 to alkali metal in the alkali CA 022130~0 1997-08-1~ .

metal catalyst is generally from about 0.001 to about 1, and in one embodiment about 0.01 to about 0.5, and in one embodiment about 0.01 to about 0.1, and in one embodiment about 0.01 to about 0.05.
The heterocyclic compounds are made by charging the reactants to a reactor, and stirring, generally without heating, since the reaction is normally exothermic. Once the reaction reaches the temperature of the exotherm (typically up to about 50~C), the reaction mixture is held at that temperature to insure complete reaction. After a reaction time of typically about 1 to about 8 hours, the volatile materials are removed under reduced pressure and the residue is filtered to yield the final product. The reaction can be conducted in the presence of a solvent, examples of which include tetrahydrofuran, diethylether, and the like.
The preparation of heterocyclic compounds within the scope of Formula (E-l) is disclosed in U.S. Patents 3,409,635 and 3,448, 120. Briefly, U.S. Patent 3,409,635 discloses making compounds represented by the formula R'- C--C--R2 'C ' Il S

wherein R' and R2 are hydrogen or methyl, by reacting CS2 with a compound represented by the formula C--C /
R1 ~ R2 CA 022130~0 1997-08-1~

at a temperature in the range of 0-50~C in the presence of a basic catalyst.
The basic catalyst is a sodium or potassium alkoxide. U.S. Patent 3,448,120 discloses the preparation of alkylene dithiocarbonates represented by the formula I
~~c~s . Il S
wherein R is hydrogen or a lower alkyl, aryl or cycloalkyl group, by reacting CS2 with a compound represented by the formula \O

at a temperature in the range of 10-70~C in the presence of a catalyst system containing an alkali metal halide (e.g., Lil, Nal, Kl, LiBr, NaBr, LiCI) and a co-catalyst selected from a sulfonium halide, a xanthate, H2S, an alkali metal sulfide, a thiocarbonate or an alcohol. These patents are incorporated herein by reference for their disclosure of processes for making heterocyclic compounds.
The following examples illustrate the preparation of the heterocyclic compounds (E) that are useful with this invention.
ExamPle E-l A mixture of 9.8 gms of LiBr, 382 gms of CS2 and 500 gms of tetrahydrofuran is placed in a reaction vessel. The reaction vessel is placed in an ice bath and the reactor contents are cooled. 839 gms of 1,2-epoxydodecane are added dropwise to the reactor contents over a period of 4 hours. An exotherm is observed. The temperature is maintained at 10-20~C. After the addition of the 1 ,2-epoxydodecane is complete, the mixture -CA 022130~0 1997-08-1~

is heated to room temperature and stripped at 20 mm Hg. The color of the reaction mixture transforms from colorless to yellow. The mixture is heated to 50~C over a period of 30 minutes and held at a pressure of 20 mm Hg absolute for one hour to remove excess CS2 and tetrahydrofuran. The mixture is cooled to room temperature and filtered through silica gel to provide 1001 gms of the desired product which is in the form of a yellow liquid and is a cyclic xanthate.
Example E-2 The following ingredients are placed in a reaction vessel: 50 gms of 1,2-epoxydodecane, 1.2 gms of LiBr, 23 gms of CS2 and 52 gms of tetrahydrofuran. The reaction vessel is closed and the ingredients are mixed at room temperature for two days. The mixture is rotary-evaporated at 70~C and 20 mm Hg for one hour. The resulting product is dissolved in a 90:10 weight ratio mixture of hexane and ethyl acetate. The mixture is chromatographed on silica gel to remove LiBr and unreacted starting material. The resulting liquid product is stripped at 50~C and 20 mm Hg to provide 55 gms of the desired product which is in the form of a red-orange liquid.
ExamPle E-3 The following ingredients are placed in a reaction vessel: 350 gms of epoxidized soybean oil, 266 gms of CS2, 7.5 gms of LiBr, and 200 gms of tetrahydrofuran. The mixture is mixed overnight at room temperature. The mixture is stripped at 70~C and 20 mm Hg and filtered to provide 350 gms of the desired product which is in the form of a yellow liquid.

CA 022130~0 1997-08-1~ .

Example E-4 The following ingredients are placed in a reaction vessel: 104 gms of CS2, 5 gms of LiBr, and 200 gms of tetrahydrofuran. The reaction vessel is placed in an ice bath. 223 gms of 2-ethylhexyl glycidyl ether are added dropwise while maintaining the temperature of the reaction mixture below 20~C. The reaction mixture is stripped at 50~C and 20 mm Hg and filtered to provide 288 gms of the desired product which is in the form of a liquid .
ExamPle E-5 The following ingredients are placed in a reaction vessel: 1267 gms of 1,2-epoxytetradecane, 500 gms of CS2, 20 gms of LiBr, and 400 gms of tetrahydrofuran. An exotherm is observed. The resulting mixture is mixed overnight. The mixture is stripped at 50~C and 20 mm Hg and filtered to provide 1724 gms of the desired product which upon cooling is in the form of a solid.
Example E-6 The following ingredients are placed in a reaction vessel: 800 gms of CS2, 20 gms of LiBr, and 200 gms of tetrahydrofuran. The reaction vessel is placed in an ice bath and the reactor contents are cooled to 10~C.
1782 gms of 2-ethylhexyl glycidyl ether are added dropwise while maintaining the temperature of the reaction mixture below 30~C. The reaction mixture is stripped at 50~C and 20 mm Hg and filtered through silica gel to provide 2276 gms of the desired product which is in the form of a yellow liquid.
ExamPle E-7 The following ingredients are placed in a reaction vessel: 382 gms of CS2, 9.8 gms of LiBr, and 500 gms of tetrahydrofuran. The reaction vessel is placed in an ice bath. 839 gms of 1,2-epoxydodecane are added dropwise over a period of 4 hours. The reaction mixture is mixed for 8 hours, then is - -CA 022130~0 1997-08-1~

stripped at 70~C and 20 mm Hg and filtered through silica gel to provide 1001 gms of the desired product.
(F) Thiocarbamate.
Component ~F) is a thiocarbamate which can be represented by the formula R'R2N-C(X)S-(CR3R4)aZ (F-l) wherein in Formula (F-l), R1, R2, R3 and R4 are independently hydrogen or hydrocarbyl groups, provided thàt at least one of R' or R2 is a hydrocarbyl group; X is O or S; a is 1 or 2; and Z is a hydrocarbyl group, a hetero group (that is, a group attached through a hetero atom such as 0, N, or S), a hydroxy hydrocarbyl group, an activating group, or a group represented by the formula -(S)C(X)-NR1R2.
When a is 2, Z is an activating group. In describing Z as an "activating group," what is meant is a group which will activate an olefin to which it is attached toward nucleophilic addition by, e.g., CS2 or COS
derived intermediates. (This is reflective of a method by which this material can be prepared, by reaction of an activated olefin with CS2 or COS and an amine.) The activating group Z can be, for instance, an ester group, typically but not necessarily a carboxylic ester group of the structure -COOR5. It can also be an ester group based on a non-carbon acid, such as a sulfonic or sulfinic ester or a phosphonic or phosphinic ester. The activating group can also be any of the acids corresponding to the aforementioned esters. Z can also be an amide group, that is, based on the condensation of an acid group, preferably a carboxylic acid group, with an amine. In that case the -(CR3R4)aZ group can be derived from acrylamide.
Z can also be an ether group, -OR6; a carbonyl group, that is, an aldehyde or a ketone group; a cyano group, -CN, or an aryl group. In one embodiment Z is an ester group of the structure, -COOR5, where R5 is a hydrocarbyl group. R5 can comprise 1 to about 18 carbon atoms, and in one embodi-CA 022130~0 1997-08-1~ .

ment 1 to about 6 carbon atoms. In one embodiment R5 is methyl so that the activating group is-COOCH3.
When a is 1, Z need not be an activating group, because the moiecule is generally prepared by methods, described below, which do not involve nucleophilic addition to an activated double bond.
When Z is a hydrocarbyl or a hydroxy hydrocarbyl group, a can be zero, 1 or 2. These hydrocarbyl groups can have from 1 to about 30 carbon atoms, and in one embodiment 1 to about 18 carbon atoms, and in one embodiment 1 to about 12 carbon atoms. Examples include methyl, ethyl, propyl, n-butyl, isobutyl, pentyl, isopentyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, dodecyl, and the corresponding hydroxy-substituted hydrocarbyl groups such as hydroxymethyl, hydroxyethyl, hydroxypropyl, etc.
R3 and R4 can be, independently, hydrogen or methyl or ethyl groups. When a is 2, at least one of R3 and R4 is normally hydrogen so that this compound will be R1R2N-C~S)S-CR3HCR3R4COOR5. In one embodiment the thiocarbamate is R1R2N-C(S)S-CH2CH2COOCH3. (These materials can be derived from methyl methacrylate and methyl acrylate, respectively.) These and other materials containing appropriate activating groups are disclosed in greater detail in U.S. Patent 4,758,362, which is incorporated herein by reference.
The substituents R' and R2 on the nitrogen atom are likewise hydrogen or hydrocarbyl groups, but at least one should be a hydrocarbyl group. It is generally believed that at least one such hydrocarbyl group is desired in order to provide a measure of oil-solubility to the molecule.
However, R1 and R2 can both be hydrogen, provided the other R groups in the molecule provide sufficient oil solubility to the molecule. In practice thismeans that at least one of the groups R3 or R4 should be a hydrocarbyl group of at least 4 carbon atoms. In one embodiment, R1 and R2 can be indepen-dently hydrocarbyl groups (e.g., aliphatic hydrocarbyl groups such as alkyl -CA 022130~0 1997-08-1~

groups) of 1 to about 50 carbon atoms, and in one embodiment 1 to about 30 carbon atoms, and in one embodiment 1 to about 18 carbon atoms, and in one embodiment 1 to about 12 carbon atoms, and in one embodiment 1 to about 8 carbon atoms.
In one embodiment the thiocarbamate is a compound represent-ed by the formula S O
Il 11 RlR2N-C-S-CH2CH2-C-OR5 (F-ll) wherein in Formula (F-ll) R', R2 and R5 are independently hydrocarbyl (e.g., alkyl) groups. These hydrocarbyl groups can have from 1 to about 18 carbon atoms, and in one embodiment 1 to about 12 carbon atoms, and in one embodiment 1 to about 8 carbon atoms, and in one embodiment 1 to about 4 carbon atoms. These compounds include S-carbomethoxyethyl-N,N-dibutyl dithiocarbamate which can be represented by the formula S O
Il 11 (C4Hg)2N-C-S-CH2CH2C-OCH3 (F-lll) Materials of this type can be prepared by a process described in U.S. Patent 4,758,362. Briefly, these materials are prepared by reacting an amine, carbon disulfide or carbonyl sulfide, or source materials for these reactants, and a reactant containing an activated, ethylenically-unsaturated bond or derivatives thereof. These reactants are charged to a reactor and stirred, generally without heating, since the reaction is normally exothermic.
Once the reaction reaches the temperature of the exotherm (typically 40-65~C), the reaction mixture is held at the temperature to insure complete reaction. After a reaction time of typically 3-5 hours, the volatile materials CA 022130~0 1997-08-1~ .

are removed under reduced pressure and the residue is filtered to yield the final product.
The' relative amounts of the reactants used to prepare these compounds are not critical. The charge ratios to the reactor can vary where economics and the amount of the product desired are controlling factors.
Thus, the molar charge ratio of the amine to the CS2 or COS reactant to the ethylenically unsaturated reactant may vary in the ranges 5:1:1 to 1:5:1 to 1:1:5. In one embodiment, the charge ratios of these reactants is 1:1:1.
In the case where a is 1, the activating group Z is separated from the sulfur atom by a methylene group. Materials of this type can be prepared by reaction of sodium dithiocarbamate with a chlorine-substituted material. Such materials are described in greater detail in U.S. Patent 2,897,152, which is incorporated herein by reference.
The following example illustrates the preparation of a thiocar-bamate (F) that can be used with this invention.
ExamPle F-1 Carbon disulfide (79.8 grams, 1.05 moles) and methyl acrylate (86 grams, 1.0 mole) are placed in a reactor and stirred at room tempera-ture. Di-n-butylamine (129 grams, 1.0 mole) is added dropwise to the mixture. The resulting reaction is exothermic, and the di-n-butylamine addition is done at a sufficient rate to maintain the temperature at 55~C.
After the addition of di-n-butylamine is complete, the reaction mixture is maintained at 55~ C for four hours. The mixture is blown with nitrogen at 85~C for one hour to remove unreacted starting material. The reaction mixture is filtered through filter paper, and the resulting product is a viscousorange liquid.
Lubricating ComPositions and Functional Fluids.
The lubricating compositions and functional fluids of the present invention are based on diverse oils of lubricating viscosity, including natural and synthetic lubricating oils and mixtures thereof. The lubricating -CA 022130~0 1997-08-1~

compositions may be lubricating oils and greases useful in industrial applica-tions and in automotive engines, transmissions and axles. These lubricating compositions are effective in a variety of applications including crankcase lubricating oils for spark-ignited and compression-ignited internal combustion engines, including automobile and truck engines, two-cycle engines, aviation piston engines, marine and low-load diesel engines, and the like. Also, automatic transmission fluids, farm tractor fluids, transaxle lubricants, gear lubricants, metalworking lubricants, hydraulic fluids, and other lubricating oiland grease compositions can beriefit from the incorporation of the composi-tions of this invention. The inventive lubricating compositions are particular-ly effective as engine lubricating oils having enhanced antiwear properties.
The lubricant compositions of this invention employ an oil of lubricating viscosity which is generally present in a major amount (i.e. an amount greater than about 50% by weight). Generally, the oil of lubricating viscosity is present in an amount greater than about 60%, or greater than about 70%, or greater than about 80% by weight of the composition.
The natural oils useful in making the inventive lubricants and functional fluids include animal oils and vegetable oils (e.g., castor oil, lardoil) as well as mineral lubricating oils such as liquid petroleum oils and solvent treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types. Oils of lubricating viscosity derived from coal or shale are also useful. Synthetic lubricating oils include hydrocarbon oils such as polymerized and interpolymerized olefins (e.g., polybutylenes, polypropylenes, propylene-isobutylene copolymers, etc.);
poly(1-hexenes), poly-(1-octenes), poly(1-decenes), etc. and mixtures thereof; alkylbenzenes (e.g., dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)benzenes, etc.); polyphenyls (e.g., biphenyls, terphenyls, alkylated polyphenyls, etc.); alkylated diphenyl ethers and alkylated diphenyl sulfides and the derivatives, analogs and homologs thereof and the like.

CA 022130~0 1997-08-1~

Alkylene oxide polymers and interpolymers and derivatives thereof where the terminal hydroxyl groups have been modified by esterification, etherification, etc., constitute another class of known synthetic lubricating oils that can be used. These are exemplified by the oils prepared through polymerization of ethylene oxide or propylene oxide, the alkyl and aryl ethers of these polyoxyalkylene polymers (e.g., methyl-poly-isopropylene glycol ether having an average molecular weight of about 1000, diphenyl ether of polyethylene glycol having a molecular weight of about 500-1000, diethyl ether of polypropylene glycol having a molecular weight of about 1000-1500, etc.) or mono- and polycarboxylic esters thereof, for example, the acetic acid esters, mixed C3.8 fatty acid esters, or the Cl30xo acid diester of tetraethylene glycol.
Another suitable class of synthetic lubricating oils that can be used comprises the esters of dicarboxylic acids (e.g., phthalic acid, succinic acid, alkyl succinic acids, alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer, malonic acid, alkyl malonic acids, alkenyl malonic acids, etc.) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoether, propylene glycol, etc.) Specific examples of these esters include dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dimer, the complex ester formed by reacting one mole of sebacic acid with two moles of tetraethylene glycol and two moles of 2-ethylhexanoic acid and the like.
Esters useful as synthetic oils also include those made from C5 to C,2 monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylol propane, pentaerythritol, dipentaerythritol, tripentaery-thritol, etc.

-CA 022130~0 1997-08-1~

Silicon-based oils such as the polyalkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane oils and silicate oils comprise another useful class of synthetic lubricants ~e.g., tetraethyl silicate, tetraisopropyl silicate, tetra-(2-ethylhexyl)silicate, tetra-(4-methylhexyl)silicate, tetra-(p-tert-butyl-phenyl) silicate, hexyl-(4-methyl-2-pentoxy)disiloxane, poly(methyl) silox-anes, poly-(methylphenyl)siloxanes, etc.). Other synthetic lubricating oils include liquid esters of phosphorus-containing acids (e.g., tricresyl phos-phate, trioctyl phosphate, diethyl ester of decanephosphonic acid, etc.), polymeric tetrahydrofurans and the like.
Unrefined, refined and rerefined oils, either natural or synthetic (as well as mixtures of two or more of any of these) of the type disclosed hereinabove can be used in the lubricants of the present invention.
Unrefined oils are those obtained directly from a natural or synthetic source without further purification treatment. For example, a shale oil obtained directly from retorting operations, a petroleum oil obtained directly from primary distillation or ester oil obtained directly from an esterification process and used without further treatment would be an unrefined oil. Refined oils are similar to the unrefined oils except they have been further treated in one or more purification steps to improve one or more properties. Many such purification techniques are known to those skilled in the art such as solvent extraction, secondary distillation, acid or base extraction, filtration, percola-tion, etc. Rerefined oils are obtained by processes similar to those used to obtain refined oils applied to refined oils which have been already used in service. Such rerefined oils are also known as reclaimed or reprocessed oils and often are additionally processed by techniques directed to removal of spent additives and oil breakdown products.
In one embodiment, component (A) is employed in the lubricant or functional fluid at a concentration in the range of about 0.001% to about 5% by weight, and in one embodiment about 0.01% to about 3%, and in one embodiment about 0.02% to about 2% by weight based on the total -CA 022130~0 1997-08-1~ .

weight of the lubricant or functional fluid. In one embodiment, component (B) is employed in the lubricant or functional fluid at a concentration in the range of about 0.01% to about 20% by weight, and in one embodiment from about 0.1% to about 10%, and in one embodiment from about 0.5%
to about 10% by weight based on the total weight of the lubricant or functional fluid. In one embodiment, component (C) is employed in the lubricant or functional fluid at a concentration in the range of up to about 20% by weight, and in one embodiment from about 0.01% to about 10%, and in one embodiment from about 0.05% to about 5% by weight based on the total weight of the lubricant or functional fluid. In one embodiment, component (D) is employed in the lubricant or functional fluid at a concentra-tion in the range of up to about 10% by weight, and in one embodiment about 0.01 % to about 5%, and in one embodiment about 0.1 % to about 3%
by weight based on the total weight of the lubricant or functional fluid. In one embodiment, component (E) is employed in the lubricant or functional fluid at a concentration in the range of up to about 10% by weight, and in one embodiment about 0.001% to about 5% by weight, and in one embodiment about 0.01% to about 3%, and in one embodiment about 0.02% to about 2% by weight based on the total weight of the lubricant or functional fluid. In one embodiment, component (F) is employed in the lubricant or functional fluid at a concentration in the range of up to about 10% by weight, and in one embodiment about 0.01% to about 5%, and in one embodiment about 0.1% to about 3% by weight based on the total weight of the lubricant or functional fluid.
In one embodiment these lubricating compositions and functional fluids have a'phosphorus content of up to about 0.12% by weight, and in one embodiment up to about 0.11% by weight, and in one embodiment up to about 0.10% by weight, and in one embodiment up to about 0.09% by weight, and in one embodiment up to about 0.08% by weight, and in one embodiment up to about 0.05% by weight. In one CA 022130~0 1997-08-1~

embodiment the phosphorus content is in the range of about 0.01% to about 0.12% by weight, and in one embodiment about 0.01% to about 0.10% by weight, and in one embodiment about 0.02% to about 0.09% by weight and in one embodiment about 0.05% to about 0.09% by weight.
The invention also provides for the use of lubricants and functional fluids containing other additives in addition to components (A), (B), (C), (D), and (F). Such additives include, for example, detergents and dispersants, corrosion-inhibiting agents, antioxidants, viscosity improving agents, extreme pressure (E.P.r agents, pour point depressants, friction modifiers, fluidity modifiers, anti-foam agents, etc.
The inventive lubricating compositions and functional fluids can contain one or more detergents or dispersants of the ash-producing or ashless type. The ash-producing detergents are exemplified by oil-soluble neutral and basic salts of alkali or alkaline earth metals with sulfonic acids, carboxylic acids, or organic phosphorus acids characterized by at least one direct carbon-to-phosphorus linkage such as those prepared by the treatment of an olefin polymer (e.g., polyisobutene having a molecular weight of 1000) with a phosphorizing agent such as phosphorus trichloride, phosphorus heptasulfide, phosphorus pentasulfide, phosphorus trichloride and sulfur, white phosphorus and a sulfur halide, or phosphorothioic chloride. The most commonly used salts of such acids are those of sodium, potassium, lithium, calcium, magnesium, strontium and barium.
Ashless detergents and dispersants are so called despite the factthat, depending on its constitution, the dispersant may upon combustion yield a non-volatile material such as boric oxide or phosphorus pentoxide;
however, it does not ordinarily contain metal and therefore does not yield a metal-containing ash on combustion. Many types are known in the art, and any of them are suitable for use in the lubricant compositions and functional fluids of this invention. The following are illustrative:

CA 022130~0 1997-08-1~

(1) Reaction products of carboxylic acids (or derivatives thereof) containing at least about 34 and preferably at least about 54 carbon atoms with nitrogen containing compounds such as amine, organic hydroxy compounds such as phenols and alcohols, and/or basic inorganic materials.
Examples of these "carboxylic dispersants" are described in many U.S.
Patents including 3,219,666; 4,234,435; and 4,938,881.
(2) Reaction products of relatively high molecular weight aliphatic or alicyclic halides with amines, preferably oxyalkylene polyamines.
These may be characterized as ~'amine dispersants" and examples thereof are described for example, in the following U.S. Patents: 3,275,554;
3,438,757; 3,454,555; and 3,565,804.
(3) Reaction products of alkyl phenols in which the alkyl group contains at least about 30 carbon atoms with aldehydes (especially formaldehyde) and amines (especially polyalkylene polyamines), which may be characterized as "Mannich dispersants." The materials described in the following U.S. Patents are illustrative: 3,649,229; 3,697,674; 3,725,277;
3,725,480; 3,726,882; and 3,980,569.
(4) Products obtained by post-treating the amine or Mannich dispersants with such reagents as urea, thiourea, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitriles, epoxides, boron compounds, phosphorus compounds or the like. Exemplary materials of this kind are described in the following U.S.
Patents: 3,639,242; 3,649,229; 3,649,659; 3,658,836; 3,697,574;
3,702,757; 3,703,536; 3,704,308; and 3,708,422.
(5) Interpolymers of oil-solubilizing monomers such as decyl methacrylate, vinyl decyl ether and high molecular weight olefins with monomers containing polar substituents, e.g., aminoalkyl acrylates or acrylamides and poly-~oxyethylene)-substituted acrylates. These may be characterized as "polymeric dispersants" and examples thereof are disclosed CA 022130~0 1997-08-1~

in the following U.S. Patents: 3,329,658; 3,449,250; 3,519,565;
3,666,730; 3,687,849; and 3,702,300.
The above-noted patents are incorporated by reference herein for their disclosures of ashless dispersants.
The inventive lubricating compositions and functional fluids can contain one or more extreme pressure, corrosion inhibitors and/or oxidation inhibitors in addition to those that would be considered as being within the scope of the above-discussed components. Extreme pressure agents and corrosion- and oxidation-inhibiting agents which may be included in the lubricants and functional fluids of the invention are exemplified by chlori-nated aliphatic hydrocarbons such as chlorinated wax; organic sulfides and polysulfides such as benzyl disulfide, bis(chlorobenzyl)disulfide, dibutyl tetrasulfide, sulfurized methyl ester of oleic acid, sulfurized alkylphenol, sulfurized dipentene, and sulfurized terpene; phosphosulfurized hydrocarbons such as the reaction product of a phosphorus sulfide with turpentine or methyl oleate; metal thiocarbamates, such as zinc dioctyldithiocarbamate, and barium heptylphenyldithiocarbamate; dithiocarbamate esters from the reaction product of dithiocarbamic acid and acrylic, methacrylic, maleic, fumaric or itaconic esters; dithiocarbamate containing amides prepared from dithiocarbamic acid and an acrylamide; alkylene-coupled dithiocarbamates;
sulfur-coupled dithiocarbamates. Many of the above-mentioned extreme pressure agents and oxidation-inhibitors also serve as antiwear agents.
Pour point depressants are a useful type of additive often included in the lubricating oils and functional fluids described herein. The use of such pour point depressants in oil-based compositions to improve low temperature properties of oil-based compositions is well known in the art.
See, for example, page 8 of "Lubricant Additives" by C.V. Smallheer and R.
Kennedy Smith (Lezius Hiles Co. publishers, Cleveland, Ohio, 1967).
Examples of useful pour point depressants are polymethacrylates; polyacryl-ates; polyacrylamides; condensation products of haloparaffin waxes and CA 022130~0 1997-08-1~ .

aromatic compounds; vinyl carboxylate polymers; and terpolymers of dialkylfumarates, vinyl esters of fatty acids and alkyl vinyl ethers. A specificpour point depressant that can be used is the product made by alkylating naphthalene with polychlorinated paraffin and C,6-ClB alpha-olefin. Pour point depressants useful for the purposes of this invention, techniques for their preparation and their uses are described in U.S. Patents 2,387,501;
2,015,748; 2,65~,479; 1,815,022; 2,191,498; 2,666,746; 2,721,877;
2,721,878; and 3,250,715 which are herein incorporated by reference for their relevant disclosures.
Anti-foam agents are used to reduce or prevent the formation of stable foam. Typical anti-foam agents include silicones or organic polymers. Additional antifoam compositions are described in "Foam Control Agents," by Henry T. Kerner (Noyes Data Corporation, 1976), pages 125-162.
Each of the foregoing additives, when used, is used at a functionally effective amount to impart the desired properties to the lubricant or functional fluid. Thus, for example, if an additive is a dispersant, a functionally effective amount of this dispersant would be an amount sufficient to impart the desired dispersancy characteristics to the lubricant or functional fluid. Similarly, if the additive is an extreme-pressure agent, a functionally effective amount of the extreme-pressure agent would be a sufficient amount to improve the extreme-pressure characteristics of the lubricant or functional fluid. Generally, the concentration of each of these additives, when used, ranges from about 0.001 % to about 20% by weight, and in one embodiment about 0.01 % to about 10% by weight based on the total weight of the lubricant or functional fluid.
The lubricant compositions of the present invention may be in the form of lubricating oils or greases in which any of the above-described oils of lubricating viscosity can be employed as a vehicle. Where the lubricant is to be used in the form of a grease, the lubricating oil generally CA 022130~0 1997-08-1~

is employed in an amount sufficient to balance the total grease composition and generally, the grease compositions will contain various quantities of thickening agents and other additive components of the type described above to provide desirable properties. Generally, the greases will contain from about 0.01 to about 20-30% of such additive components.
A wide variety of thickening agents can be used in the preparation of the greases of this invention. Included among the thickening agents are alkali and alkaline earth metal soaps of fatty acids and fatty materials having from about 12 to about 30 carbon atoms. The metals are typified by sodium, lithium, calcium and barium. Examples of fatty materials include stearic acid, hydroxy stearic acid, stearin, oleic acid, palmetic acid, myristic acid, cottonseed oil acids, and hydrogenated fish oils.
Other thickening agents include salt and salt-soap complexes as calcium stearate-acetate ( U . S. Patent 2, 1 97, 263), barium stearate acetate (U.S. Patent2,564,561 ),calciumstearate-caprylate-acetatecomplexes~U.S.
Patent 2,999,065), calcium caprylate-acetate (U.S. Patent 2,999,066), and calcium salts and soaps of low-, intermediate- and high-molecular weight acids and of nut oil acids.
Useful thickening agents employed in the grease compositions are essentially hydrophilic in character, but which have been converted into a hydrophobic condition by the introduction of long chain hydrocarbon radicals onto the surface of the clay particles prior to their use as a component of a grease composition, as, for example, by being subjected to a preliminary treatment with an organic cationic surface-active agent, such as an onium compound. Typical onium compounds are tetraalkylammonium chlorides, such as dimethyl dioctadecyl ammonium chloride, dimethyl dibenzyl ammonium chloride and mixtures thereof. This method of conversion, being well known to those skilled in the art, and is believed to require no further discussion. More specifically, the clays which are useful as starting materials in forming the thickening agents to be employed in the CA 022130~0 1997-08-1~

grease compositions, can comprise the naturally occurring chemically unmodified clays. These clays are crystalline complex silicates, the exact composition of which is not subject to precise description, since they vary widely from one natural source to another. These clays can be described as complex inorganic silicates such as aluminum silicates, magnesium silicates, barium silicates, and the like, containing, in addition to the silicate iattice,varying amounts of cation-exchangeable groups such as sodium.
Hydrophilic clays which are particularly useful for conversion to desired thickening agents include montmorillonite clays, such as bentonite, attapulgite, hectorite, illite, saponite, sepiolite, biotite, vermiculite, zeolite clays, and the like. The thickening agent is generally employed in an amount from about 0.5 to about 30% by weight, and in one embodiment from about 3% to about 15% by weight of the total grease composition.
Components (A) and (B), and optional components (C) to (F) of the inventive compositions as well as one of the other above-discussed additives or other additives known in the art can be added directly to the lubricant or functional fluid. In one embodiment, however, they are diluted with a substantially inert, normally liquid organic diluent such as mineral oil,naphtha, benzene, toluene or xylene to form an additive concentrate which is then added to the base oil to form the lubricant or functional fluid. These concentrates usually contain from about 1% to about 99% by weight, and in one embodiment about 10% to about 90% by weight of components (A) and (B) and, optionally, one or more of components (C) to (F) as well as one or more other additives known in the art or described hereinabove. The remainder of the concentrate is the substantially inert normally liquid diluent.The following Examples 1-37 illustrate lubricating compositions and functional fluids within the scope of the invention.

CA 022130~0 1997-08-1~

Example 1 Wt. %
Product of Example A-1 0.5 Product of Example B-1 5.0 Base oil Remainder ExamPle 2 Wt. %
Product of Example A-2 1.0 Product of Example B-1 4.0 Base oil Remainder ExamPle 3 Wt. %
Product of Example A-3 1.4 Product of Example B-1 6.0 Base oil Remainder ExamPle 4 Wt. %
Product of Example A-1 0.7 Product of Example B-2 4.5 Base oil Remainder ExamPle 5 Wt. %
Product of Example A-2 2.0 Product of Example B-2 6.5 Base oil Remainder ExamPle 6 Wt. %
Product of Example A-3 0.3 Product of Example B-2 6.5 Base oil Remainder - - - ~ - - - - -CA 022130~0 1997-08-1~

Exam Ple 7 Wt. %
Product of Example A-4 0.5 Product of Example B-1 5.0 Base oil Remainder ExamPle 8 Wt. %
Product of Example A-5 1.0 Product of Example B-1 4.0 Base oil Remainder ExamPle 9 Wt. %
Product of Example A-6 1.4 Product of Example B-1 6.0 Base oil Remainder Example 10 Wt. %
Product of Example A-7 0.7 Product of Example B-1 4.5 Base oil Remainder ExamPle 1 1 Wt. %
Product of Example A-5 2.0 Product of Example B-2 6.5 Base oil Remainder ExamPle 12 Wt. %
Product of Example A-7 0.3 Product of Example B-2 6.5 Base oil Remainder CA 022130~0 1997-08-1~

ExamPle 13 Wt. %
Product of Example A-8 0.5 Product of Example B-1 5.0 Base oil Remainder ExamPle 14 Wt. %
Product of Example A-9 1.0 Product of Example B- 1 4.0 Base oil Remainder ExamPle 15 Wt. %
Product of Example A-10 1.4 Product of Example B-1 6.0 Base oil Remainder Example 16 Wt. %
Product of Example A-11 0.7 Product of Example B-1 4.5 Base oil Remainder ExamPle 17 Wt. %
Product of Example A-9 2.0 Product of Example B-2 6.5 Base oil Remainder Example 18 Wt. %
Prod uct of Example A- 1 1 0. 3 Product of Example B-2 6.5 Base oil Remainder -CA 022130~0 1997-08-1~

Exa,..l~le 19 Wt. %
Product of Example A-1 2.5 Product of Example B-1 5.0 Product of Example C-1 0.5 Base oil Remainder ExamDle 20 Wt. %
Product of Example A-2 0.5 Product of Example B-1 4.0 Product of Example C- 1 0.7 Base oil Remainder ExamDle 21 Wt. %
Product of Example A-3 1.5 Product of Example B-1 5.0 Product of Example C-1 0.5 Base oil Remainder Exal,.pl~ 22 Wt. %
Product of Example A-1 1.0 Product of Example B-2 5.0 Product of Example C-1 0.3 Base oil Remainder ExamDle 23 Wt. %
Product of Example A-2 0.3 Product of Example B-2 4.5 Product of Example C-1 0.7 Base oil Remainder CA 022130~0 1997-08-1~

ExamPle 24 Wt. %
Product of Example A-3 1.0 Product of Example B-2 5. 5 Product of Example C-1 0.5 Base oil Remainder Example 25 Wt. %
Product of Example A-1 1.1 Product of Example B-1 6.5 Product of Example C-2 0.5 Base oil Remainder ExamPle 26 Wt. %
Product of Example A-1 0.9 Product of Example B-1 5.0 Product of Example C-7(a) 0.7 Base oil Remainder Example 27 Wt. %
Product of Example A-1 0.8 Product of Example B- 1 4. 5 Product of Example C-7(b) . 1.4 Base oil Remainder ExamPle 28 Wt. %
Product of Example A-1 1.2 Product of Example B-1 6.0 Product of Example C-7(c) 0. 5 Base oil Remainder CA 022130~0 1997-08-1~

ExamPle 29 Wt. %
Product of Example A-1 1.2 Product of Example B-1 5.0 Product of Example D-1 0.6 Base oil Remainder ExamPle 30 Wt. %
Product of Example A-1 0.6 Product of Example B-1 5.0 Product of Example E-1 0.5 Base oil Remainder ExamPle 31 Wt. %
Product of Example A-1 1.5 Product of Example B-1 4.5 Product of Example F-1 0.5 Base oil Remainder ExamPle 32 Wt. %
Product of Example A-1 1.5 Product of Example B-1 4.5 Product of Example B-2 3.0 Product of Example D-1 0.5 Base oil Remainder CA 022130~0 1997-08-1~

ExamPle 33 Wt. %
Product of Example A-1 1.5 Prod uct of Example B- 1 5 . 5 Product of Example B-2 2.5 Product of Example E-1 0.5 Base oil Remainder Exa~ lc 34 Wt. %
1 0 Product of Example A- 1 1 . 5 Prodùct of Example B-1 4.5 Product of Example B-2 3.5 Product of Example F-1 0.5 Base oil Remainder 1 5 ExamPle 35 Wt. %
Product of Example A-1 0.5 Product of Example B-1 5.5 Product of Example C-1 1.0 Product of Example D-1 0.5 Base oil Remainder Exam~le 36 Wt. %
Product of Example A-1 1.0 Product of Example B-1 5.5 Product of Example C-1 0.5 Product of Example D-1 0.25 Product of Example E-1 0.25 Base oil Remainder CA 022130~0 1997-08-1~

ExamPle 37 Wt. %
Product of Example A-1 0.5 Product of Example B-1 5.0 Product of Example C-1 1.5 Product of Example D-1 0.5 Product of Example E- 1 0. 5 Product of Example F-1 0.5 Base oil Remainder Examples 38-40 disclosed in Table I are provided for the purpose of further illustrating lubricating compositions within the scope of the invention. These compositions are useful as engine lubricating oil compositions. In Table I all numerical values, except for the concentration of the silicone antifoam agent are in percent by weight. The concentration of the silicone antifoam agent is in parts per million, ppm.

CA 022130~0 1997-08-1~

Table I

Examr~le No. 38 39 40 Base oil ~85% 100N + 15% 150N) 80.9 80.9 80.9 Product of Example A-1 0.5 -- --Product of Example A-5 -- 0.5 --Prod uct of Example A- 11 -- -- 0.5 Product of Example B-1 4.03 4.03 4.03 Product of Example B-2 1.37 1.37 1.37 Product of Example C-1 0.72 0.72 0.72 Overbased Mg sulfonate, 0.45 0.45 0.45 metal/sulfonate ratio = 14.7, oil content s 42%
Overbased Ca sulfonate, 0.22 0.22 0.22 metal/sulfonate ratio = 1.2, oil content = 50%
Overbased Na succinate, 0.2 0.2 0.2 oil content = 49%
Ca overbased sulfur coupled 0.5 0.5 0.5 alkyl phenol, oil content = 39%
Olefin copolymer Vl improver 0.7 0.7 0.7 Alkylated diphenylamine 0.6 0.6 0.6 Polymethacrylate pour point 0.2 0.2 0.2 depressant Sulfur monochloride reacted with 0.3 0.3 0.3 alpha olefin mixture followed by contact with sodium disulfide Vegetable oil 0.1 0.1 0.1 Diluent oil 8.3 8.3 8.3 Silicone antifoam agent, ppm 18 18 18 Phosphorus content 0.072 0.072 0.072 CA 022130~0 1997-08-1~

While the invention has been explained in relation to its preferred embodiments, it is to be understood that various modifications thereof will become apparent to those skilled in the art upon reading the specification. Therefore, it is to be understood that the invention disclosed herein is intended to cover such modifications as fall within the scope of the appended claims.

Claims

1. A composition, comprising:
(A) a compound represented by the formula S
¦
R1-X-C-S-(CR2R3)nT (A-I) wherein in Formula (A-I): R1, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;
with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different; and (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms.

2. The composition of claim 1 further comprising:
(C) a phosphorus compound.

3. The composition of claim 1 further comprising:
(D) a compound represented by the formula ¦ ¦
G1-C-S-(S)n-C-G2 (D-1) wherein in Formula (D-1), G1 and G2 are independently R, OR, SR or NRR
wherein each R is independently a hydrocarbyl group, X1 and X2 are independently O or S, and n is zero to 3.

4. The composition of claim 1 further comprising:
(E) a compound represented by the formula (E-I) wherein in Formula (E-I): X1, X2 and X3 are independently O or S, and X2 and X3 can be NR1 wherein R1 is hydrogen or hydrocarbyl; and G1, G2, G3 and G4 are independently R2, OR2 or R3OR2, wherein R2 is hydrogen or hydrocarbyl and R3 is hydrocarbylene or hydrocarbylidene.

5. The composition of claim 1 further comprising:
(F) a compound represented by the formula R1R2N-C(X)S-(CR3R4)aZ (F-I) wherein in Formula (F-I), R1, R2, R3 and R4 are independently hydrogen or hydrocarbyl groups, provided that at least one of R1 and R2 is a hydrocarbyl group; X is O or S; a is 1 or 2, provided that when a is 2, each CR3R4 can be the same or different; and Z is a hydrocarbyl group, a hetero group, a hydroxy hydrocarbyl group, an activating group, or a -(S)C(X)NR1R2 group;
provide that when a is 2, Z is an activating group.

6. The composition of claim 1 wherein in Formula (A-I), T
is -R, -OR, -R*OR, -COR, -COOR, -R*COR, -R*COOR, -CONRR, -R*CONRR, -COO(R*O)tR, -R*COO(R*O)tR, -CN, -R*CN, O O O O
¦ ¦ ¦ ¦
-SR, -R*SR, -SOR, -R*SOR, O O O O
¦ ¦ ¦ ¦
-SR, -R*SR, -S-OR, -R*S-OR
¦ ¦ ¦ ¦
O O O S

wherein each R is independently hydrogen or a hydrocarbyl group, and each R* is independently a hydrocarbylene or hydrocarbylidene group, and t is number of at least 1.

7. The composition of claim 1 wherein n is zero, and T is a metal selected from the group consisting of Group IA, IIA or IIB metals, aluminum, tin, iron, cobalt, lead, molybdenum, manganese, nickel, antimony, bismuth, or a mixture of two or more thereof.

8. The composition of claim 1 wherein in Formula (A-I), X
is S, and R1 and T are independently hydrocarbyl groups.

9. The composition of claim 1 wherein in Formula (A-I), X
is O, and R1 and T are independently hydrocarbyl groups.

10. The composition of claim 1 wherein component (A) is a compound represented by the formula S
¦
R1-X-C-S-R (A-II) wherein in Formula (A-II), R1 and R are independently hydrogen or hydrocarbyl groups, and X is O or S.

11. The composition of claim 1 wherein component (A) is a compound represented by the formula S O
¦ ¦
R1-X-C-S-R2-C-O(R3O)tR4 (A-III) wherein in Formula (A-III), R1 and R4 are independently hydrogen or hydrocarbyl groups, R2 and R3 are independently hydrocarbylene or hydrocarbylidene groups, X is O or S, and t is 1 to about 8.

12. The composition of claim 1 wherein said acylated nitrogen-containing compound (B) is derived from a carboxylic acylating agent and at least one amino compound containing at least one -NH- group, said acylating agent being linked to said amino compound through an imido, amido, amidine or salt linkage.

13. The composition of claim 1 wherein (B) is derived from a substituted succinic acid or anhydride, the substituent groups on said succinic acid or anhydride being derived from polybutene in which at least about 50% of the total units derived from butenes are derived from isobutylene, said polybutene being characterized by an ~n value of about 1500 to about 2000 and an ~w/~n value of about 3 to about 4, said acid or anhydride being characterized within its structure of an average of about 1.5 to about 2.5 succinic groups for each equivalent weight of substituent groups.

14. The composition of claim 1 wherein (B) is derived from a substituted succinic acid or anhydride, the substituent groups on said succinic acid or anhydride being derived from polybutene in which at least about 50% of the total units derived from butenes are derived from isobutylene, said polybutene being characterized by an ~n value of about 800 to about 1200 and an ~w/~n value of about 2 to about 3, said acid or anhydride being characterized within its structure of an average of about 0.9 to about 1.2 succinic groups for each equivalent weight of substituent groups.

15. The composition of claim 2 wherein (C) is a phosphorus acid, phosphorus acid ester, phosphorus acid salt, or derivative thereof.

16. The composition of claim 2 wherein (C) is a compound represented by the formula (C-I) wherein in Formula (C-I), R1, R2 and R3 are independently hydrogen or hydrocarbyl groups, X is O or S, and a, b and c are independently zero or 1.

17. The composition of claim 2 wherein (C) is a compound represented by the formula (C-II) wherein in Formula (C-II), R1, R2 and R3 are independently hydrogen or hydrocarbyl groups, and a, b and c are independently zero or 1.

18. The composition of claim 2 wherein (C) is a compound represented by the formula (C-III) wherein in Formula (C-III): X1, X2 and X3 and X4 are independently O or S, and X1 and X2 can be NR4; a and b are independently zero or 1; and R1, R2, R3 and R4 are independently hydrocarbyl groups, and R3 and R4 can be hydrogen; or a metal, amine or ammonium salt of said compound represented by Formula (C-III).

19. The composition of claim 18 wherein said compound represented by Formula (C-III) is a metal salt, said metal being a Group IA, IIA or IIB metal, aluminum, tin, iron, cobalt, lead, molybdenum, manganese, nickel, antimony, bismuth, or a mixture of two or more thereof.

20. The composition of claim 18 wherein said compound represented by Formula (C-III) is a metal salt, said metal being zinc.

21. The composition of claim 2 wherein (C) is a compound represented by the formula ¦ ¦
R1O-P-S-(S)n-P-OR3 (C-IV) / \

wherein in Formula (C-IV), R1, R2, R3 and R4 are independently hydrocarbyl groups, X1 and X2 are independently O or S, and n is zero to 3.

22. The composition of claim 3 wherein in Formula (D-I), G1 and G2 are OR or SR, X1 and X2 are S, and n is 1.

23. The composition of claim 4 wherein in Formula (E-I), G1 is R2, OR2 or R3OR2; G2, G3 and G4 are hydrogen; and X1, X2 and X3 are S.

24. The composition of claim 5 wherein (F) is a compound represented by the formula S O
¦ ¦
R1R2N-C-S-CH2CH2-C-OR5 (F-II) wherein in Formula (F-II), R1, R2 and R5 are independently hydrocarbyl groups.

25. The composition of claim 5 wherein (F) is a compound represented by the formula S O
¦ ¦
(C4H9)2N-C-S-CH2CH2-C-OCH3 (F-III)

26. The composition of claim 1 further comprising a corrosion-inhibiting agent, detergent, dispersant, antioxidant, viscosity improving agent, antiwear agent, extreme-pressure agent, pour-point depressant, friction-modifier, fluidity-modifier, anti-foam agent, or mixture oftwo or more thereof.

27. A composition, comprising:
(A) a compound represented by the formula S
¦
R1-X-C-S-R (A-II) wherein in Formula (A-II), X is O or S, R1 and R are independently hydrogen or hydrocarbyl groups; and (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms.

28. A composition, comprising:
(A) a compound represented by the formula S
¦
R1-X-C-S-R (A-II) wherein in Formula (A-II): X is O or S; and R1 and R are independently hydrogen or hydrocarbyl groups;
(B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms; and (C) a phosphorus compound.

29. A process comprising mixing:
(A) a compound represented by the formula S
¦
R1-X-C-S-(CR2R3)nT (A-I) wherein in Formula (A-I): R1, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;
with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different; and (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms.

30. A process comprising mixing:
(A) a compound represented by the formula S
¦
R1-X-C-S-(CR2R3)nT (A-I) wherein in Formula (A-I): R1, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group, with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different;
(B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms; and (D) a compound represented by the formula ¦ ¦
G1-C-S-(S)n-C-G2 (D-I) wherein in Formula (D-1), G1 and G2 are independently R, OR, SR or NRR
wherein each R is independently a hydrocarbyl group, X1 and X2 are independently O or S, and n is zero to 3.

31. A process comprising mixing:
(A) a compound represented by the formula S
¦
R1-X-C-S-(CR2R3)nT (A-I) wherein in Formula (A-I): R1, R2 and R3 are independently hydrogen or hydrocarbyl groups; X is O or S; n is zero, 1 or 2; and T is a hydrocarbyl group, a hetero group, a hydroxyhydrocarbyl group, or an activating group;
with the proviso that when n is zero, T can be a metal, and when n is 2, each R2 and R3 can be the same or different (B) an acylated nitrogen-containing compound having a substituent of at least about 10 carbon atoms; and (C) a phosphorus compound.

32. A concentrate comprising a diluent and from about 1%
to about 99% by weight of the composition of claim 1.

33. A lubricant or functional fluid comprising a major amount of an oil of lubricating viscosity and a minor antiwear amount of the composition of claim 1.

34. An engine lubricating oil composition comprising a major amount of an oil of lubricating viscosity and a minor antiwear amount of the composition of claim 1.

35. A process for making a lubricant or a functional fluid comprising mixing an oil of lubricating viscosity with the composition of claim 1.

36. A process for making a lubricant or a functional fluid, comprising:
(1) mixing the composition of claim 1 with a diluent to form a concentrate; and (2) mixing the concentrate of step (1) with an oil of lubricating viscosity to form said lubricant or functional fluid.