CA1041985A - Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle - Google Patents

Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle

Info

Publication number: CA1041985A
Authority: CA; Canada
Prior art keywords: alkyl; succinic acid; alkenyl succinic; water; ester
Prior art date: 1976-09-03
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

CA260,512A

Other languages

English (en)

Inventor

Robert H. Davis

John W. Schick

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.)

Mobil Oil AS

Original Assignee

Mobil Oil AS

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.)

1976-09-03

Filing date

1976-09-03

Publication date

1978-11-07

1976-09-03 Application filed by Mobil Oil AS filed Critical Mobil Oil AS

1976-09-03 Priority to CA260,512A priority Critical patent/CA1041985A/fr

1978-11-07 Application granted granted Critical

1978-11-07 Publication of CA1041985A publication Critical patent/CA1041985A/fr

Status Expired legal-status Critical Current

Links

-1 amine salts Chemical class 0.000 title claims abstract description 18
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 title claims abstract description 11
125000000217 alkyl group Chemical group 0.000 title claims abstract description 11
239000000203 mixture Substances 0.000 title claims abstract description 10
239000000314 lubricant Substances 0.000 title abstract description 16
239000001384 succinic acid Substances 0.000 title abstract description 7
239000012530 fluid Substances 0.000 claims abstract description 16
230000003115 biocidal effect Effects 0.000 claims abstract description 12
150000002148 esters Chemical class 0.000 claims abstract description 9
238000005555 metalworking Methods 0.000 claims abstract description 9
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims abstract description 7
239000003139 biocide Substances 0.000 claims abstract description 4
239000013556 antirust agent Substances 0.000 claims abstract description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
150000003839 salts Chemical class 0.000 claims description 5
GGQRKYMKYMRZTF-UHFFFAOYSA-N 2,2,3,3-tetrakis(prop-1-enyl)butanedioic acid Chemical compound CC=CC(C=CC)(C(O)=O)C(C=CC)(C=CC)C(O)=O GGQRKYMKYMRZTF-UHFFFAOYSA-N 0.000 claims description 3
239000010953 base metal Substances 0.000 claims 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
125000006724 (C1-C5) alkyl ester group Chemical group 0.000 abstract 1
239000003921 oil Substances 0.000 description 12
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 9
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 8
150000001412 amines Chemical class 0.000 description 8
235000011044 succinic acid Nutrition 0.000 description 8
239000000654 additive Substances 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
229910001296 Malleable iron Inorganic materials 0.000 description 4
238000005260 corrosion Methods 0.000 description 4
239000002562 thickening agent Substances 0.000 description 4
229960004418 trolamine Drugs 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
230000001580 bacterial effect Effects 0.000 description 3
230000009849 deactivation Effects 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000463 material Substances 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
239000002826 coolant Substances 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
239000010730 cutting oil Substances 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
230000009036 growth inhibition Effects 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000001050 lubricating effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
ULSIYEODSMZIPX-UHFFFAOYSA-N phenylethanolamine Chemical compound NCC(O)C1=CC=CC=C1 ULSIYEODSMZIPX-UHFFFAOYSA-N 0.000 description 2
230000002265 prevention Effects 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
238000010186 staining Methods 0.000 description 2
239000012085 test solution Substances 0.000 description 2
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
OJPDDQSCZGTACX-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)anilino]ethanol Chemical compound OCCN(CCO)C1=CC=CC=C1 OJPDDQSCZGTACX-UHFFFAOYSA-N 0.000 description 1
BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
PVCJKHHOXFKFRP-UHFFFAOYSA-N N-acetylethanolamine Chemical compound CC(=O)NCCO PVCJKHHOXFKFRP-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
241000589516 Pseudomonas Species 0.000 description 1
206010037660 Pyrexia Diseases 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000005233 alkylalcohol group Chemical group 0.000 description 1
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 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
150000001669 calcium Chemical class 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
239000002173 cutting fluid Substances 0.000 description 1
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
229910001651 emery Inorganic materials 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003349 gelling agent Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000008233 hard water Substances 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000003879 lubricant additive Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
239000006078 metal deactivator Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229950006768 phenylethanolamine Drugs 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003444 succinic acids Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
230000008719 thickening Effects 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1

Landscapes

Lubricants (AREA)

CA260,512A 1976-09-03 1976-09-03 Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle Expired CA1041985A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA260,512A CA1041985A (fr)	1976-09-03	1976-09-03	Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA260,512A CA1041985A (fr)	1976-09-03	1976-09-03	Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle

Publications (1)

Publication Number	Publication Date
CA1041985A true CA1041985A (fr)	1978-11-07

Family

ID=4106784

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA260,512A Expired CA1041985A (fr)	1976-09-03	1976-09-03	Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle

Country Status (1)

Country	Link
CA (1)	CA1041985A (fr)

1976
- 1976-09-03 CA CA260,512A patent/CA1041985A/fr not_active Expired

Publication	Publication Date	Title
US4053426A (en)	1977-10-11	Lubricant compositions
CA1039293A (fr)	1978-09-26	Lubrifiants
JP2902281B2 (ja)	1999-06-07	水溶性金属防食剤
US6984340B1 (en)	2006-01-10	Corrosion inhibiting formulations
US4957641A (en)	1990-09-18	Use of alkoxyhydroxy fatty acids as corrosion inhibitors in oils and oil-containing emulsions
US2481372A (en)	1949-09-06	Rust protective lubricants
JPS58171488A (ja)	1983-10-08	潤滑油組成物
US4289636A (en)	1981-09-15	Aqueous lubricant compositions
US4107060A (en)	1978-08-15	Lubricant compositions containing biocidal, antirust additives
JPH01308495A (ja)	1989-12-13	ホスファイトアミン潤滑添加剤
CA1245211A (fr)	1988-11-22	Methode de travail mecanique de metal renfermant du cobalt et concentre convenant a cette fin, apres dilution a l'eau
JPH06502887A (ja)	1994-03-31	オイル組成物
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US4218329A (en)	1980-08-19	Cooling and lubricating fluid for metal working
US3769214A (en)	1973-10-30	Aqueous lubricant compositions containing alkanolamine salts of carboxylic acids
JPH03229631A (ja)	1991-10-11	新規な耐生分解性界面活性剤およびそれを利用する切削油配合物
US5348670A (en)	1994-09-20	Phosphorous amine lubricant additives
US4414125A (en)	1983-11-08	Alkali metal or amine salts of a mixture of 2- and 3-alkyladipic acids as corrosion inhibitors
US2316903A (en)	1943-04-20	Addition agent for lubricants
US2605226A (en)	1952-07-29	Compounded lubricating oil
CA1041985A (fr)	1978-11-07	Lubrifiant contenant des sels amines de demi-esters d'acide succinique alkyle ou alcenyle
US2516838A (en)	1950-08-01	Soluble oil base
US5316696A (en)	1994-05-31	Composition
US6204228B1 (en)	2001-03-20	Light-colored sulfur-containing extreme pressure lubricant additives