ES2620681T3 - Lubricación de motores marinos - Google Patents

Lubricación de motores marinos Download PDF

Info

Publication number: ES2620681T3
Authority: ES; Spain
Prior art keywords: composition; oil; engine; lubricating; hydrocarbyl
Prior art date: 2014-12-04
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.): Active

Application number

ES15195322.1T

Other languages

English (en)

Spanish (es)

Inventor

Tushar Bera

Rachel Tundel

Laura Gregory

Peter Wright

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.)

Infineum International Ltd

Original Assignee

Infineum International Ltd

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.)

2014-12-04

Filing date

2015-11-19

Publication date

2017-06-29

2014-12-04 Priority claimed from US14/560,231 external-priority patent/US9879202B2/en

2015-10-27 Priority claimed from US14/923,535 external-priority patent/US10364404B2/en

2015-11-19 Application filed by Infineum International Ltd filed Critical Infineum International Ltd

2017-06-29 Application granted granted Critical

2017-06-29 Publication of ES2620681T3 publication Critical patent/ES2620681T3/es

Status Active legal-status Critical Current

2035-11-19 Anticipated expiration legal-status Critical

Links

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WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
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230000002378 acidificating effect Effects 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
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238000005054 agglomeration Methods 0.000 description 1
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150000004703 alkoxides Chemical class 0.000 description 1
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239000012298 atmosphere Substances 0.000 description 1
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BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
WLLCYXDFVBWGBU-UHFFFAOYSA-N bis(8-methylnonyl) nonanedioate Chemical compound CC(C)CCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC(C)C WLLCYXDFVBWGBU-UHFFFAOYSA-N 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
VBIGULIJWJPALH-UHFFFAOYSA-L calcium;2-carboxyphenolate Chemical class [Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O VBIGULIJWJPALH-UHFFFAOYSA-L 0.000 description 1
AVVIDTZRJBSXML-UHFFFAOYSA-L calcium;2-carboxyphenolate;dihydrate Chemical compound O.O.[Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O AVVIDTZRJBSXML-UHFFFAOYSA-L 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
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230000021523 carboxylation Effects 0.000 description 1
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239000000567 combustion gas Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
DZQISOJKASMITI-UHFFFAOYSA-N decyl-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound CCCCCCCCCCP(O)(O)=O DZQISOJKASMITI-UHFFFAOYSA-N 0.000 description 1
230000008021 deposition Effects 0.000 description 1
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150000001993 dienes Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
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238000006073 displacement reaction Methods 0.000 description 1
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238000011067 equilibration Methods 0.000 description 1
239000010696 ester oil Substances 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
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238000004880 explosion Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
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150000004665 fatty acids Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
230000014509 gene expression Effects 0.000 description 1
238000007429 general method Methods 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
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230000002140 halogenating effect Effects 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
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230000002209 hydrophobic effect Effects 0.000 description 1
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150000002500 ions Chemical class 0.000 description 1
238000005304 joining Methods 0.000 description 1
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239000011968 lewis acid catalyst Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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238000004519 manufacturing process Methods 0.000 description 1
230000013011 mating Effects 0.000 description 1
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150000004692 metal hydroxides Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
239000000693 micelle Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000003345 natural gas Substances 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
PJLHTVIBELQURV-UHFFFAOYSA-N pentadecene Natural products CCCCCCCCCCCCCC=C PJLHTVIBELQURV-UHFFFAOYSA-N 0.000 description 1
238000005325 percolation Methods 0.000 description 1
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229920000573 polyethylene Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
235000013824 polyphenols Nutrition 0.000 description 1
229920006389 polyphenyl polymer Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
229920001384 propylene homopolymer Polymers 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
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239000003079 shale oil Substances 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
238000000629 steam reforming Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
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CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
235000011044 succinic acid Nutrition 0.000 description 1
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
150000001911 terphenyls Chemical class 0.000 description 1
JZALLXAUNPOCEU-UHFFFAOYSA-N tetradecylbenzene Chemical class CCCCCCCCCCCCCCC1=CC=CC=C1 JZALLXAUNPOCEU-UHFFFAOYSA-N 0.000 description 1
MQHSFMJHURNQIE-UHFFFAOYSA-N tetrakis(2-ethylhexyl) silicate Chemical compound CCCCC(CC)CO[Si](OCC(CC)CCCC)(OCC(CC)CCCC)OCC(CC)CCCC MQHSFMJHURNQIE-UHFFFAOYSA-N 0.000 description 1
ZUEKXCXHTXJYAR-UHFFFAOYSA-N tetrapropan-2-yl silicate Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)OC(C)C ZUEKXCXHTXJYAR-UHFFFAOYSA-N 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
238000004448 titration Methods 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
ZAGXLQIHXTXRFW-UHFFFAOYSA-N tris(2-ethyl-4-methylhexyl)-tris(2-ethyl-4-methylhexyl)silyloxysilane Chemical compound CCC(C)CC(CC)C[Si](CC(CC)CC(C)CC)(CC(CC)CC(C)CC)O[Si](CC(CC)CC(C)CC)(CC(CC)CC(C)CC)CC(CC)CC(C)CC ZAGXLQIHXTXRFW-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M165/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/04—Molecular weight; Molecular weight distribution
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/52—Base number [TBN]
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Chemistry (AREA)
Lubricants (AREA)
Engineering & Computer Science (AREA)
Combustion & Propulsion (AREA)
Mechanical Engineering (AREA)
Ocean & Marine Engineering (AREA)

ES15195322.1T 2014-12-04 2015-11-19 Lubricación de motores marinos Active ES2620681T3 (es)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
US201414560231		2014-12-04
US14/560,231 US9879202B2 (en)	2014-12-04	2014-12-04	Marine engine lubrication
EP15153647		2015-02-03
EP15153647		2015-02-03
US201514923535		2015-10-27
US14/923,535 US10364404B2 (en)	2014-12-04	2015-10-27	Marine engine lubrication

Publications (1)

Publication Number	Publication Date
ES2620681T3 true ES2620681T3 (es)	2017-06-29

Family

ID=54540992

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES15195322.1T Active ES2620681T3 (es)	2014-12-04	2015-11-19	Lubricación de motores marinos

Country Status (8)

Country	Link
EP (1)	EP3029133B1 (fr)
JP (1)	JP6777395B2 (fr)
KR (1)	KR102481890B1 (fr)
CN (2)	CN105670746A (fr)
AU (1)	AU2015264882B2 (fr)
CA (1)	CA2913603C (fr)
ES (1)	ES2620681T3 (fr)
SG (1)	SG10201509951RA (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP3421576B8 (fr) *	2017-06-30	2021-09-08	Infineum International Limited	Procédé anti-encrassement de raffinerie
CA3064222C (fr)	2018-12-20	2025-02-18	Infineum International Limited	Mazout marin d’hydrocarbures
SG10201911804SA (en) *	2018-12-20	2020-07-29	Infineum Int Ltd	Oil anti-foulant and/or asphaltene agglomeration process

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1248643B (de)	1959-03-30	1967-08-31	The Lubrizol Corporation, Cleveland, Ohio (V. St. A.)	Verfahren zur Herstellung von öllöslichen aeylierten Aminen
US3231587A (en)	1960-06-07	1966-01-25	Lubrizol Corp	Process for the preparation of substituted succinic acid compounds
US3215707A (en)	1960-06-07	1965-11-02	Lubrizol Corp	Lubricant
US3087936A (en)	1961-08-18	1963-04-30	Lubrizol Corp	Reaction product of an aliphatic olefinpolymer-succinic acid producing compound with an amine and reacting the resulting product with a boron compound
US3381022A (en)	1963-04-23	1968-04-30	Lubrizol Corp	Polymerized olefin substituted succinic acid esters
NL296139A (fr)	1963-08-02
US3574576A (en)	1965-08-23	1971-04-13	Chevron Res	Distillate fuel compositions having a hydrocarbon substituted alkylene polyamine
US3272746A (en)	1965-11-22	1966-09-13	Lubrizol Corp	Lubricating composition containing an acylated nitrogen compound
US3442808A (en)	1966-11-01	1969-05-06	Standard Oil Co	Lubricating oil additives
US3912764A (en)	1972-09-29	1975-10-14	Cooper Edwin Inc	Preparation of alkenyl succinic anhydrides
US4110349A (en)	1976-06-11	1978-08-29	The Lubrizol Corporation	Two-step method for the alkenylation of maleic anhydride and related compounds
DE2702604C2 (de)	1977-01-22	1984-08-30	Basf Ag, 6700 Ludwigshafen	Polyisobutene
US4234435A (en)	1979-02-23	1980-11-18	The Lubrizol Corporation	Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation
GB8818711D0 (en) *	1988-08-05	1988-09-07	Shell Int Research	Lubricating oil dispersants
US4952739A (en)	1988-10-26	1990-08-28	Exxon Chemical Patents Inc.	Organo-Al-chloride catalyzed poly-n-butenes process
CA1335895C (fr)	1989-02-07	1995-06-13	Exxon Chemical Patents Inc.	Methode basse temperature utilisant un melange en zone multiple pour l'obtention de derives de substitution par une longue chaine hydrocarbylee d'acides mono- ou dicarboxyliques
CA1338288C (fr)	1989-02-07	1996-04-30	Jai Gopal Bansal	Methode de preparation de derives de substitution hydrocarbyles a longue chaine d'acides dicarboxyliques
IL107927A0 (en)	1992-12-17	1994-04-12	Exxon Chemical Patents Inc	Oil soluble ethylene/1-butene copolymers and lubricating oils containing the same
CA2110654C (fr)	1992-12-17	2006-03-21	Albert Rossi	Procede pour la polymerisation d'un copolymere ethylene-alpha-olefine utilisant des catalyseurs a base de metallocene, en milieu dilue
TW291486B (fr)	1992-12-17	1996-11-21	Exxon Chemical Patents Inc
US5334321A (en)	1993-03-09	1994-08-02	Chevron Research And Technology Company, A Division Of Chevron U.S.A. Inc.	Modified high molecular weight succinimides
US5777025A (en)	1996-02-09	1998-07-07	Exxon Chemical Patents Inc.	Process for preparing polyalkenyl substituted C4 to C10 dicarboxylic acid producing materials
US5891953A (en)	1996-02-09	1999-04-06	Exxon Chemical Patents Inc	Process for preparing polyalkenyl substituted mono- and dicarboxylic acid producing materials (PT-1302)
US6165235A (en) *	1997-08-26	2000-12-26	The Lubrizol Corporation	Low chlorine content compositions for use in lubricants and fuels
GB9908771D0 (en) *	1999-04-17	1999-06-09	Infineum Uk Ltd	Lubricity oil composition
JP2004256668A (ja) *	2003-02-26	2004-09-16	Mitsui Chemicals Inc	ポリアルキレンコハク酸無水物の製造方法
US7339007B2 (en)	2003-06-20	2008-03-04	Infineum International Limited	Low sediment process for thermally reacting highly reactive polymers and enophiles
US7956022B2 (en)	2005-07-29	2011-06-07	Chevron Oronite Company Llc	Low sulfur metal detergent-dispersants
US20080128184A1 (en) *	2006-11-30	2008-06-05	Loper John T	Lubricating oil compositions having improved corrosion and seal protection properties
EP2155657B1 (fr) *	2007-06-08	2017-05-03	Infineum International Limited	Additifs et compositions d'huiles de graissage les contenant
EP2123739B1 (fr) *	2008-05-20	2017-09-27	Infineum International Limited	Lubrification de moteur marin
US20120028521A1 (en) *	2009-04-07	2012-02-02	Terence Garner	Marine engine lubrication
EP2424965B1 (fr) *	2009-05-01	2015-05-20	Infineum International Limited	Lubrification de moteur marin
US8349776B2 (en) *	2009-09-29	2013-01-08	Chevron Oronite Company Llc	Trunk piston engine lubricating oil compositions
GB2496732B (en) *	2011-11-17	2014-03-12	Infineum Int Ltd	Marine engine lubrication
EP2644687B1 (fr) *	2012-03-29	2016-09-28	Infineum International Limited	Lubrification de moteur marin
ES2586531T3 (es) *	2012-11-21	2016-10-17	Infineum International Limited	Lubricación de motor marino
EP2765179B1 (fr) *	2013-02-07	2016-09-28	Infineum International Limited	Lubrification de moteur marin

2015
- 2015-11-19 ES ES15195322.1T patent/ES2620681T3/es active Active
- 2015-11-19 EP EP15195322.1A patent/EP3029133B1/fr active Active
- 2015-11-30 CA CA2913603A patent/CA2913603C/fr active Active
- 2015-12-03 CN CN201510882756.8A patent/CN105670746A/zh active Pending
- 2015-12-03 AU AU2015264882A patent/AU2015264882B2/en active Active
- 2015-12-03 JP JP2015236868A patent/JP6777395B2/ja active Active
- 2015-12-03 CN CN202211019360.7A patent/CN115353926A/zh active Pending
- 2015-12-03 SG SG10201509951RA patent/SG10201509951RA/en unknown
- 2015-12-03 KR KR1020150171342A patent/KR102481890B1/ko active Active

Also Published As

Publication number	Publication date
EP3029133B1 (fr)	2017-03-15
JP6777395B2 (ja)	2020-10-28
AU2015264882A1 (en)	2016-06-23
AU2015264882B2 (en)	2016-12-08
KR102481890B1 (ko)	2022-12-28
CN105670746A (zh)	2016-06-15
EP3029133A1 (fr)	2016-06-08
KR20160067774A (ko)	2016-06-14
CN115353926A (zh)	2022-11-18
CA2913603A1 (fr)	2016-06-04
SG10201509951RA (en)	2016-07-28
CA2913603C (fr)	2023-01-03
JP2016108565A (ja)	2016-06-20

Publication	Publication Date	Title
ES2425957T3 (es)	2013-10-18	Lubricación de motor marino
ES2608805T3 (es)	2017-04-17	Lubricación de motor marino
ES2646051T3 (es)	2017-12-11	Lubricación de motores marinos
ES2586531T3 (es)	2016-10-17	Lubricación de motor marino
ES2612336T3 (es)	2017-05-16	Lubrificación de motor marino
ES2620681T3 (es)	2017-06-29	Lubricación de motores marinos
ES2712955T3 (es)	2019-05-16	Lubricación de motor marino
US10364404B2 (en)	2019-07-30	Marine engine lubrication
US9879202B2 (en)	2018-01-30	Marine engine lubrication