JPH0138159B2 - - Google Patents

Info

Publication number: JPH0138159B2
Authority: JP; Japan
Prior art keywords: oil; additive; lubricating oil; carbon atoms; acid
Prior art date: 1980-04-18
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP56054250A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5710695A (en

Inventor

Shidonii Haasuteitsuku Kurisuchan

Terii Uendoraa Kenesu

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Edwin Cooper Inc

Original Assignee

Edwin Cooper Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1980-04-18

Filing date

1981-04-10

Publication date

1989-08-11

1981-04-10 Application filed by Edwin Cooper Inc filed Critical Edwin Cooper Inc

1982-01-20 Publication of JPS5710695A publication Critical patent/JPS5710695A/ja

1989-08-11 Publication of JPH0138159B2 publication Critical patent/JPH0138159B2/ja

Status Granted legal-status Critical Current

Links

-1 alkyl primary amine salt Chemical group 0.000 claims description 47
239000003921 oil Substances 0.000 claims description 22
239000010687 lubricating oil Substances 0.000 claims description 17
125000000217 alkyl group Chemical group 0.000 claims description 12
239000000446 fuel Substances 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 10
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 8
238000002485 combustion reaction Methods 0.000 claims description 7
239000000314 lubricant Substances 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
239000000654 additive Substances 0.000 description 33
230000000996 additive effect Effects 0.000 description 23
239000000203 mixture Substances 0.000 description 18
239000002270 dispersing agent Substances 0.000 description 14
238000012360 testing method Methods 0.000 description 13
235000014113 dietary fatty acids Nutrition 0.000 description 11
150000002148 esters Chemical class 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
239000000194 fatty acid Substances 0.000 description 11
150000004665 fatty acids Chemical class 0.000 description 11
239000011701 zinc Substances 0.000 description 10
229910052725 zinc Inorganic materials 0.000 description 10
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 9
229910052784 alkaline earth metal Inorganic materials 0.000 description 9
150000001412 amines Chemical class 0.000 description 9
239000004215 Carbon black (E152) Substances 0.000 description 8
229930195733 hydrocarbon Natural products 0.000 description 8
239000003208 petroleum Substances 0.000 description 8
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 6
229920002367 Polyisobutene Polymers 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
239000002480 mineral oil Substances 0.000 description 5
230000007935 neutral effect Effects 0.000 description 5
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 5
229920000098 polyolefin Polymers 0.000 description 5
229910052791 calcium Inorganic materials 0.000 description 4
239000011575 calcium Substances 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
FPYLHOQPWCQAIJ-UHFFFAOYSA-N 1-dimethoxyphosphoryloctadecane Chemical compound CCCCCCCCCCCCCCCCCCP(=O)(OC)OC FPYLHOQPWCQAIJ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
235000010446 mineral oil Nutrition 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000010705 motor oil Substances 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
229920000768 polyamine Polymers 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
230000003068 static effect Effects 0.000 description 3
235000011044 succinic acid Nutrition 0.000 description 3
150000003871 sulfonates Chemical class 0.000 description 3
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 3
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
239000005642 Oleic acid Substances 0.000 description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001342 alkaline earth metals Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000004996 alkyl benzenes Chemical class 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
239000004327 boric acid Substances 0.000 description 2
239000003599 detergent Substances 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000003502 gasoline Substances 0.000 description 2
150000003949 imides Chemical class 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000003607 modifier Substances 0.000 description 2
150000002763 monocarboxylic acids Chemical class 0.000 description 2
229940049964 oleate Drugs 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid group Chemical group C(CCC(=O)O)(=O)O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
150000003444 succinic acids Chemical class 0.000 description 2
229960002317 succinimide Drugs 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
239000013638 trimer Substances 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
WJECKFZULSWXPN-UHFFFAOYSA-N 1,2-didodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCC WJECKFZULSWXPN-UHFFFAOYSA-N 0.000 description 1
KDMAJIXYCNOVJB-UHFFFAOYSA-N 2,2-bis(nonanoyloxymethyl)butyl nonanoate Chemical compound CCCCCCCCC(=O)OCC(CC)(COC(=O)CCCCCCCC)COC(=O)CCCCCCCC KDMAJIXYCNOVJB-UHFFFAOYSA-N 0.000 description 1
YQMSJAXVJVDRSO-UHFFFAOYSA-N 2-methylhenicosan-2-amine Chemical compound CCCCCCCCCCCCCCCCCCCC(C)(C)N YQMSJAXVJVDRSO-UHFFFAOYSA-N 0.000 description 1
ISJZMDCFBCMXCK-UHFFFAOYSA-N 2-methylnonadecan-2-amine Chemical compound CCCCCCCCCCCCCCCCCC(C)(C)N ISJZMDCFBCMXCK-UHFFFAOYSA-N 0.000 description 1
OWEJNUBCZDCKRT-UHFFFAOYSA-N 2-methylpentadecan-2-amine Chemical compound CCCCCCCCCCCCCC(C)(C)N OWEJNUBCZDCKRT-UHFFFAOYSA-N 0.000 description 1
WXBXQUFGRJEKPL-UHFFFAOYSA-N 2-methylundecan-2-amine Chemical compound CCCCCCCCCC(C)(C)N WXBXQUFGRJEKPL-UHFFFAOYSA-N 0.000 description 1
ANHQLUBMNSSPBV-UHFFFAOYSA-N 4h-pyrido[3,2-b][1,4]oxazin-3-one Chemical group C1=CN=C2NC(=O)COC2=C1 ANHQLUBMNSSPBV-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
238000006683 Mannich reaction Methods 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
AOZDHFFNBZAHJF-UHFFFAOYSA-N [3-hexanoyloxy-2,2-bis(hexanoyloxymethyl)propyl] hexanoate Chemical compound CCCCCC(=O)OCC(COC(=O)CCCCC)(COC(=O)CCCCC)COC(=O)CCCCC AOZDHFFNBZAHJF-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
125000000746 allylic group Chemical group 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
239000002199 base oil Substances 0.000 description 1
SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
150000001639 boron compounds Chemical class 0.000 description 1
SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
239000002738 chelating agent Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
HIKZOIYUQFYFBB-UHFFFAOYSA-N didodecyl decanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCCCCCC HIKZOIYUQFYFBB-UHFFFAOYSA-N 0.000 description 1
GHKVUVOPHDYRJC-UHFFFAOYSA-N didodecyl hexanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCC GHKVUVOPHDYRJC-UHFFFAOYSA-N 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
239000010710 diesel engine oil Substances 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000007429 general method Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
AGDYNDJUZRMYRG-UHFFFAOYSA-N hexyl nitrate Chemical compound CCCCCCO[N+]([O-])=O AGDYNDJUZRMYRG-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
ZLNMGXQGGUZIJL-UHFFFAOYSA-N n-octyl-n-phenylnaphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(CCCCCCCC)C1=CC=CC=C1 ZLNMGXQGGUZIJL-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
229910052761 rare earth metal Inorganic materials 0.000 description 1
150000002910 rare earth metals Chemical class 0.000 description 1
238000007670 refining Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
JDVPQXZIJDEHAN-UHFFFAOYSA-N succinamic acid Chemical class NC(=O)CCC(O)=O JDVPQXZIJDEHAN-UHFFFAOYSA-N 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
229940072690 valium Drugs 0.000 description 1
PXJZGBFRKRTOPA-UHFFFAOYSA-L zinc;[2,3-di(nonyl)phenyl]sulfanyl-dioxido-sulfanylidene-$l^{5}-phosphane Chemical compound [Zn+2].CCCCCCCCCC1=CC=CC(SP([O-])([O-])=S)=C1CCCCCCCCC PXJZGBFRKRTOPA-UHFFFAOYSA-L 0.000 description 1

Landscapes

Lubricants (AREA)

JP5425081A 1980-04-18 1981-04-10 Lubricant oil containing tertiary amine salt of sulfidized olefinic acid Granted JPS5710695A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US14168280A	1980-04-18	1980-04-18

Publications (2)

Publication Number	Publication Date
JPS5710695A JPS5710695A (en)	1982-01-20
JPH0138159B2 true JPH0138159B2 (es)	1989-08-11

Family

ID=22496740

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5425081A Granted JPS5710695A (en)	1980-04-18	1981-04-10	Lubricant oil containing tertiary amine salt of sulfidized olefinic acid

Country Status (1)

Country	Link
JP (1)	JPS5710695A (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6174900U (es) *	1984-10-20	1986-05-20
US8304181B2 (en)	2004-10-07	2012-11-06	Transmedics, Inc.	Method for ex-vivo organ care and for using lactate as an indication of donor organ status
US12010987B2 (en)	2004-10-07	2024-06-18	Transmedics, Inc.	Systems and methods for ex-vivo organ care and for using lactate as an indication of donor organ status
IL311989A (en)	2004-10-07	2024-06-01	Transmedics Inc	Methods and systems for extracorporeal organ treatment
US9078428B2 (en)	2005-06-28	2015-07-14	Transmedics, Inc.	Systems, methods, compositions and solutions for perfusing an organ
US9457179B2 (en)	2007-03-20	2016-10-04	Transmedics, Inc.	Systems for monitoring and applying electrical currents in an organ perfusion system
CN106659151B (zh)	2014-06-02	2021-06-08	特兰斯迈迪茨公司	离体器官护理***
CN112933394B (zh)	2015-09-09	2023-10-24	特兰斯迈迪茨公司	用于在离体器官护理***中使用的主动脉插管

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1990365A (en) *	1932-03-21	1935-02-05	Standard Oil Co	Top cylinder lubricant

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3755176A (en) *	1971-05-14	1973-08-28	Mobil Oil Corp	Sulfur-containing carboxylic acids as corrosion inhibitors

1981
- 1981-04-10 JP JP5425081A patent/JPS5710695A/ja active Granted

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1990365A (en) *	1932-03-21	1935-02-05	Standard Oil Co	Top cylinder lubricant

Also Published As

Publication number	Publication date
JPS5710695A (en)	1982-01-20

Publication	Publication Date	Title
US3367943A (en)	1968-02-06	Process for preparing oil soluble additives which comprises reacting a c2 to c5 alkylene oxide with (a) reaction product of an alkenylsuccinic anhydride and an aliphaticpolyamine (b) reaction product of alkenylsuccinic anhydride, a c1 to c30 aliphatic hydrocarbon carboxylic acid and an aliphatic polyamine
US4495088A (en)	1985-01-22	Method for improving fuel economy of internal combustion engines
US4455243A (en)	1984-06-19	Succinimide complexes of borated fatty acid esters of glycerol and lubricating oil compositions containing same
EP0020037B1 (en)	1984-08-15	Oil-soluble friction-reducing additive, process for the preparation thereof, and lubricating oil or fuel composition containing the additive
US4192757A (en)	1980-03-11	Alkyl phenol solutions of organo molybdenum complexes as friction reducing antiwear additives
US3637499A (en)	1972-01-25	Amine derivatives of dithiophosphoric acid compounds
US4325827A (en)	1982-04-20	Fuel and lubricating compositions containing N-hydroxymethyl succinimides
US4643838A (en)	1987-02-17	Normally liquid C18 to C24 monoalkyl catechols
US5164102A (en)	1992-11-17	Lubricating oil composition
US4394277A (en)	1983-07-19	Method for improving fuel economy of internal combustion engines using borated sulfur-containing 1,2-alkane diols
EP0072645A2 (en)	1983-02-23	Improved succinimide lubricating oil dispersant
US3224968A (en)	1965-12-21	Lubricating oil compositions
US4228020A (en)	1980-10-14	Lubricating oil composition
US3359203A (en)	1967-12-19	Ashless dithiophosphoric acid derivatives
US3454496A (en)	1969-07-08	Lubricant compositions
JPH0138159B2 (es)	1989-08-11
JPH0438793B2 (es)	1992-06-25
US4356097A (en)	1982-10-26	Alkylphosphonate lubricating oil
US4629577A (en)	1986-12-16	Method for improving fuel economy of internal combustion engines
US4960528A (en)	1990-10-02	Lubricating oil composition
US4938882A (en)	1990-07-03	Borated and non-borated overbased carboxylates as corrosion inhibitors
CA1273344A (en)	1990-08-28	Succinimide complexes of borated alkyl catechols and lubricating oil compositions containing same
US4243538A (en)	1981-01-06	Fuel and lubricating compositions containing N-hydroxymethyl aliphatic hydrocarbylamide friction reducers
US5028345A (en)	1991-07-02	Lubricating oil composition
CA1224470A (en)	1987-07-21	Succinimide complexes of borated fatty acid esters of glycerol and lubricating compositions containing same