GB1440273A - Aclated nitrogen compounds - Google Patents
Aclated nitrogen compoundsInfo
- Publication number
- GB1440273A GB1440273A GB5583573A GB5583573A GB1440273A GB 1440273 A GB1440273 A GB 1440273A GB 5583573 A GB5583573 A GB 5583573A GB 5583573 A GB5583573 A GB 5583573A GB 1440273 A GB1440273 A GB 1440273A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkylene
- acid
- acylating
- methyl
- triamines
- 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
Links
Classifications
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- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—Amides; Imides
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08F8/00—Chemical modification by after-treatment
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- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
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- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
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- C10L1/221—Organic compounds containing nitrogen compounds of uncertain formula; reaction products where mixtures of compounds are obtained
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1440273 Polyolefin derivatives LUBRIZOL CORP 3 Dec 1973 55835/63 Headings C3P and C3R [Also in Division C5] Oil soluble dispersants having demulsifying properties comprise reaction products obtained by acylating (I) at least one polyoxyalkylene polyamine of molecular weight at least 200 of formula H 2 N - alkylene(O alkylene) m - NH 2 or of formula R-[alkylene(O alkylene) n NH 2 ] 3-6 where m is 3-70, n is 1-40 provided that the sum of all ns is 3-70 and R is a saturated hydrocarbon radical of up to 10 carbon atoms and valence 3 to 6 with (II) a carboxylic acid acylating agent having at least 8 carbon atoms in an aliphatic substituent derived from an olefin polymer and selected from acids, anhydrides, halides and alkyl esters, in amount of at least 0À001 equivalent of (I) per equivalent of (II). The polyolefin may be derived from ethylene, propylene, butenes, hexene-1, octene-1 2-methylheptene-1, 3-cyclohexylbutene-1, 2- methyl - 5 - propylhexene - 1, 3 - pentene or 4-octene, optionally together with minor proportions of cycloolefins, aryl-substituted olefins and polyenes. The products may be added to lubricating and fuel oil compositions. Many suitable reactants are specified and examples describe the reaction of polyisobutenyl succinic anhydride prepared from chlorinated polyisobutene and maleic anhydride with (1,2 and 4-13) polyoxypropylene diamines, (3) polyoxypropylene triamines and (14) polyoxyalkylene triamines; and the reaction of polyoxyethylene diamines with acylating agents prepared from chlorinated polyisobutene and (15) methyl methacrylate, (18 and 19) acrylic acid, (21) propyl α-chloracrylate, and (22) 3-butene-1,2,3- tricarboxylic acid, 1,2-diethyl 3-methyl ester, or with (17) polyethylene substituted malonic acid dimethyl ester or an acylating agent derived from (20) chlorinated polyethylene and ethyl acrylate; polyoxyethylene triamines with acylating agents prepared from (16) brominated polyhexene-1 and 2-pentene-1,3,5-tricarboxylic acid, and from chlorinated polyisobutene and (23) triethyl, (24) trimethyl and (25) 1,2-diethyl-3-methyl esters of 3-butene-1,2,3-tricarboxylic acid; and polyoxypropylene diamines with (27) stearic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5583573A GB1440273A (en) | 1973-12-03 | 1973-12-03 | Aclated nitrogen compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5583573A GB1440273A (en) | 1973-12-03 | 1973-12-03 | Aclated nitrogen compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1440273A true GB1440273A (en) | 1976-06-23 |
Family
ID=10475014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5583573A Expired GB1440273A (en) | 1973-12-03 | 1973-12-03 | Aclated nitrogen compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1440273A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2470140A1 (en) * | 1979-11-27 | 1981-05-29 | Ppg Industries Inc | AMIDATION REACTION PRODUCTS OF POLYAMINES AND MATERIALS CONTAINING POLYCARBOXYL GROUPS AND COATING COMPOSITIONS COMPRISING THEM |
WO1995035329A1 (en) * | 1994-06-17 | 1995-12-28 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine group and secondary or tertiary amines groups |
-
1973
- 1973-12-03 GB GB5583573A patent/GB1440273A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2470140A1 (en) * | 1979-11-27 | 1981-05-29 | Ppg Industries Inc | AMIDATION REACTION PRODUCTS OF POLYAMINES AND MATERIALS CONTAINING POLYCARBOXYL GROUPS AND COATING COMPOSITIONS COMPRISING THEM |
US5643859A (en) | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
WO1995035329A1 (en) * | 1994-06-17 | 1995-12-28 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine group and secondary or tertiary amines groups |
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