GB2208517B - Middle distillate compositions with reduced wax crystal size - Google Patents

Middle distillate compositions with reduced wax crystal size

Info

Publication number
GB2208517B
GB2208517B GB8811911A GB8811911A GB2208517B GB 2208517 B GB2208517 B GB 2208517B GB 8811911 A GB8811911 A GB 8811911A GB 8811911 A GB8811911 A GB 8811911A GB 2208517 B GB2208517 B GB 2208517B
Authority
GB
United Kingdom
Prior art keywords
crystal size
middle distillate
wax crystal
distillate compositions
reduced wax
Prior art date
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 - Lifetime
Application number
GB8811911A
Other versions
GB8811911D0 (en
GB2208517A (en
Inventor
Kenneth Lewtas
Edwin William Lehmann
Richard Dix Kerwood
Kenneth William Bartz
Jacqueline Dawn Bland
David Paul Gillingham
John Edward Maddox
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.)
ExxonMobil Chemical Patents Inc
Original Assignee
Exxon Chemical Patents 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.)
Filing date
Publication date
Priority claimed from GB08622961A external-priority patent/GB2197878A/en
Priority claimed from GB878719423A external-priority patent/GB8719423D0/en
Application filed by Exxon Chemical Patents Inc filed Critical Exxon Chemical Patents Inc
Priority claimed from PCT/GB1987/000675 external-priority patent/WO1988002394A2/en
Publication of GB8811911D0 publication Critical patent/GB8811911D0/en
Publication of GB2208517A publication Critical patent/GB2208517A/en
Application granted granted Critical
Publication of GB2208517B publication Critical patent/GB2208517B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/01Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
    • C07C211/02Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C211/03Monoamines
    • C07C211/07Monoamines containing one, two or three alkyl groups, each having the same number of carbon atoms in excess of three
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/01Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
    • C07C211/02Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C211/03Monoamines
    • C07C211/08Monoamines containing alkyl groups having a different number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/57Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing carboxyl groups bound to the carbon skeleton
    • C07C309/58Carboxylic acid groups or esters thereof
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/57Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing carboxyl groups bound to the carbon skeleton
    • C07C309/59Nitrogen analogues of carboxyl groups
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    • C10L1/00Liquid carbonaceous fuels
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    • C10L1/14Organic compounds
    • C10L1/143Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
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    • C10L1/00Liquid carbonaceous fuels
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    • C10L1/14Organic compounds
    • C10L1/24Organic compounds containing sulfur, selenium and/or tellurium
    • C10L1/2431Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
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    • C10L1/2431Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
    • C10L1/2437Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
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    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
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    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/189Carboxylic acids; metal salts thereof having at least one carboxyl group bound to an aromatic carbon atom
    • C10L1/1895Carboxylic acids; metal salts thereof having at least one carboxyl group bound to an aromatic carbon atom polycarboxylic acid
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    • C10L1/196Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
    • C10L1/1963Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof mono-carboxylic
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    • C10L1/196Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
    • C10L1/1966Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof poly-carboxylic
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    • C10L1/1973Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and an acyloxy group of a saturated carboxylic or carbonic acid mono-carboxylic
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    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
GB8811911A 1986-09-24 1987-09-24 Middle distillate compositions with reduced wax crystal size Expired - Lifetime GB2208517B (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB08622961A GB2197878A (en) 1986-10-07 1986-09-24 Middle distillate compositions with reduced wax crystal size
DE19863634081 DE3634081A1 (en) 1986-10-07 1986-10-07 FUEL OR FUEL OIL BASED ON PETROLEUM DISTILLATES
GB878719423A GB8719423D0 (en) 1986-09-24 1987-08-17 Middle distillate compositions
PCT/GB1987/000675 WO1988002394A2 (en) 1986-09-24 1987-09-24 Middle distillate compositions with reduced wax crystal size

Publications (3)

Publication Number Publication Date
GB8811911D0 GB8811911D0 (en) 1988-07-13
GB2208517A GB2208517A (en) 1989-04-05
GB2208517B true GB2208517B (en) 1990-10-03

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2860040A (en) * 1955-05-25 1958-11-11 Exxon Research Engineering Co Petroleum distillate fuels
GB1138553A (en) * 1966-08-25 1969-01-01 Shell Int Research Method and apparatus for treating wax-bearing oil
US3481939A (en) * 1965-03-15 1969-12-02 Eastman Kodak Co Tertiaryaminocyclobutanes with electronegative substituents
FR2256235A1 (en) * 1973-12-26 1975-07-25 Exxon Research Engineering Co
FR2490669A1 (en) * 1980-09-19 1982-03-26 Elf France NOVEL ADDITIVE COMPOSITIONS FOR IMPROVING FILTRABILITY LIMIT TEMPERATURE AND SIMULTANEOUS INHIBITION OF N-PARAFFIN CRYSTALS FORMED DURING LOW TEMPERATURE STORAGE OF MEDIUM DISTILLATES
EP0061894A2 (en) * 1981-03-31 1982-10-06 Exxon Research And Engineering Company Two-component flow improver additive for middle distillate fuel oils

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2860040A (en) * 1955-05-25 1958-11-11 Exxon Research Engineering Co Petroleum distillate fuels
US3481939A (en) * 1965-03-15 1969-12-02 Eastman Kodak Co Tertiaryaminocyclobutanes with electronegative substituents
GB1138553A (en) * 1966-08-25 1969-01-01 Shell Int Research Method and apparatus for treating wax-bearing oil
FR2256235A1 (en) * 1973-12-26 1975-07-25 Exxon Research Engineering Co
FR2490669A1 (en) * 1980-09-19 1982-03-26 Elf France NOVEL ADDITIVE COMPOSITIONS FOR IMPROVING FILTRABILITY LIMIT TEMPERATURE AND SIMULTANEOUS INHIBITION OF N-PARAFFIN CRYSTALS FORMED DURING LOW TEMPERATURE STORAGE OF MEDIUM DISTILLATES
EP0061894A2 (en) * 1981-03-31 1982-10-06 Exxon Research And Engineering Company Two-component flow improver additive for middle distillate fuel oils

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
ErdÖl und Kohle-Erdgas-Petrochemie, volume 20, no. 2, February 1967, pag *
Hydrocarbon Processing, volume 54, no. 9, September 1975, pages 129-136 *
Industrial and Engineering Chemistry, volume 59, no. 5, May 1967, pages *
Journal of the Institute of Petroleum, volume 51, no. 499, July 1965, pa *
Pôtrole et Techniques, no. 312, December 1984, pages 7-18 *
Revue de l'Institut Fran×ais du P­trole, volume 34, no. 5, September-Oct *

Also Published As

Publication number Publication date
GB8811911D0 (en) 1988-07-13
GB2208517A (en) 1989-04-05

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