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Process for the preparation of aminated polymers useful as additives for fuels and lubricants

Assignee: ExxonMobil Technology and Engineering Co
•
Filing: 1975-09-15
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Granted: 1977-06-28
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Expires: 1995-09-15
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Abstract

Abstract Preparation of aminated polymeric additives useful as oil additives, for example as dispersants for hydrocarbon fuels and lubricants, and as multifunctional dispersant-viscosity index improvers for lubricants, by the reaction of amine with a halogen containing copolymer of ethylene, a C 3 to C 18 straight or branched chain α-olefin and a C 5 to C 14 acyclic or alicyclic nonconjugated diolefin, said halogen containing copolymer being prepared by the halogenation of said copolymer.

Inventors

  • 👤 Won R. Song
  • 👤 John Brooke Gardiner
  • 👤 Lawrence James Engel

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 08:54
CPC Classifications
C; C10; C10M; C10M147/00; C10M147/02; C08; C08F; C08F8/00; C08F8/30; C08F8/32; C10M1/00; C10M1/08; C10M143/00; C10M143/02; C08F2800/00; C08F2800/20; C10M2205/00; C10M2205/02; C10M2205/026; C10M2207/00; C10M2207/02; C10M2207/023; C10M2207/024; C10M2207/28; C10M2207/282; C10M2207/32; C10M2207/34; C10M2209/00; C10M2209/02; C10M2209/08; C10M2209/084; C10M2209/086; C10M2209/10; C10M2209/103; C10M2209/109; C10M2209/11; C10M2209/111; C10M2209/112; C10M2211/00; C10M2211/06; C10M2213/00; C10M2213/02; C10M2213/06; C10M2213/062; C10M2215/00; C10M2215/02; C10M2215/04; C10M2215/042; C10M2215/06; C10M2215/064; C10M2215/065; C10M2215/22; C10M2215/221; C10M2215/223; C10M2215/224; C10M2215/225; C10M2215/226; C10M2215/24; C10M2215/26; C10M2215/30; C10M2217/00; C10M2217/02; C10M2217/022; C10M2217/028; C10M2217/04; C10M2217/046; C10M2217/06; C10M2219/00; C10M2219/08; C10M2219/082; C10M2219/087; C10M2219/088; C10M2219/089; C10M2223/00; C10M2223/02; C10M2223/04; C10M2223/041; C10M2223/042; C10M2223/045; C10N; C10N2010/00; C10N2010/04; C10N2070/00; C10N2070/02

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 212 words
A method for preparing an oil-soluble, sludge dispersing, aminated copolymer, said aminated copolymer having a molecular weight in the range of about 1000 to 500,000 Mn, and containing about 0.02 to about 2.0 wt. % nitrogen, based on the weight of said aminated copolymer, comprising the steps of solution brominating a terpolymer having an olefinic double bond in a hydrocarbon moiety which is pendant to the backbone chain of carbon atoms with a brominating agent to incorporate from about 0.1 to 10 wt. % viscinally substituted bromine in said pendant hydrocarbon moiety, said terpolymer comprising ethylene, a C 3 to C 18 straight or branched chain α-olefin and a C 5 to C 14 acyclic or alicyclic non-conjugated diolefin, said solution brominating step being carried out at a temperature of from 0° to 100° C.; and thereafter aminating said brominated terpolymer with a C 1 to C 60 amine containing 1 to 12 amine groups by reacting said amine with said brominated terpolymer until from about 10 to 100 mole percent of the bromine content of said terpolymer is replaced by amination groups, said reacting being carried out at a temperature in the range of about 20° C. to about 150° C. and for a period of from 0.1 to 10 hours.
Claim 2
Independent Claim 212 words
A method for preparing an oil-soluble, sludge dispersing, aminated copolymer, said aminated copolymer having a molecular weight in the range of about 1000 to 500,000 Mn, and containing about 0.02 to about 2.0 wt. % nitrogen, based on the weight of said aminated copolymer, comprising the steps of solution brominating a terpolymer having an olefinic double bond in a hydrocarbon moiety which is pendant to the backbone chain of carbon atoms with a brominating agent to incorporate from about 0.1 to 10 wt. % viscinally substituted bromine in said pendant hydrocarbon moiety, said terpolymer comprising ethylene, a C 3 to C 18 straight or branched chain α-olefin and a C 5 to C 14 acyclic or alicyclic non-conjugated diolefin, said solution brominating step being carried out at a temperature of from 0° to 100° C.; and thereafter aminating said brominated terpolymer with a C 1 to C 60 amine containing 1 to 12 amine groups by reacting said amine with said brominated terpolymer until from about 10 to 100 mole percent of the bromine content of said terpolymer is replaced by amination groups, said reacting being carried out at a temperature in the range of about 20° C. to about 150° C. and for a period of from 0.1 to 10 hours.
Claim 3
Dependent Claim 39 words
A method according to claim 1 wherein said brominating agent is bromine and said reacting is at a temperature in the range of about 25° C. to about 120° C. and for a period of 0.5 to 5 hours.
Claim 4
Dependent Claim 13 words
In a process according to claim 1 wherein said solvent is mineral oil.
Claim 5
Dependent Claim 45 words
A process according to claim 1 wherein said molecular weight is about 20,000 to 100,000, said nitrogen content is about 0.1 to 1.0 wt. % nitrogen, and said alpha olefin is a C 3 to C 8 olefin and said solvent is a liquid hydrocarbon.
Claim 6
Dependent Claim 18 words
A process according to claim 4 wherein said terpolymer is a copolymer of ethylene, propylene and said diolefin.
Claim 7
Dependent Claim 20 words
A process according to claim 5 wherein said diolefin is selected from the group consisting of 5-ethylidene norbornene-2 and 1,4-hexadiene.
Claim 8
Dependent Claim 17 words
A process according to claim 5, wherein said amine is a poly(ethyleneamine) of 2 to 6 nitrogens.
Claim 9
Independent Claim 212 words
A method for preparing an oil-soluble, sludge dispersing, aminated copolymer, said aminated copolymer having a molecular weight in the range of about 1000 to 500,000 Mn, and containing about 0.02 to about 2.0 wt. % nitrogen, based on the weight of said aminated copolymer, comprising the steps of solution chlorinating a terpolymer having an olefinic double bond in a hydrocarbon moiety which is pendant to the backbone chain of carbon atoms with a chlorinating agent to incorporate from about 0.1 to 10 wt. % allylically substituted chlorine in said pendant hydrocarbon moiety, said terpolymer comprising ethylene, a C 3 to C 18 staight or branched chain α-olefin and a C 5 to C 14 acyclic or alicyclic non-conjugated diolefin, said solution chlorinating step being carried out at a temperature of from 0° to 100° C.; and thereafter aminating said chlorinated terpolymer with a C 1 to C 60 amine containing 1 to 12 amine groups by reacting said amine with said chlorinated terpolymer until from about 10 to 100 mole percent of the chlorine content of said terpolymer is replaced by amination groups, said reacting being carried out at a temperature in the range of about 80° C. to about 200° C. and for a period of from 3 to 100 hours.
Claim 10
Independent Claim 212 words
A method for preparing an oil-soluble, sludge dispersing, aminated copolymer, said aminated copolymer having a molecular weight in the range of about 1000 to 500,000 Mn, and containing about 0.02 to about 2.0 wt. % nitrogen, based on the weight of said aminated copolymer, comprising the steps of solution chlorinating a terpolymer having an olefinic double bond in a hydrocarbon moiety which is pendant to the backbone chain of carbon atoms with a chlorinating agent to incorporate from about 0.1 to 10 wt. % allylically substituted chlorine in said pendant hydrocarbon moiety, said terpolymer comprising ethylene, a C 3 to C 18 staight or branched chain α-olefin and a C 5 to C 14 acyclic or alicyclic non-conjugated diolefin, said solution chlorinating step being carried out at a temperature of from 0° to 100° C.; and thereafter aminating said chlorinated terpolymer with a C 1 to C 60 amine containing 1 to 12 amine groups by reacting said amine with said chlorinated terpolymer until from about 10 to 100 mole percent of the chlorine content of said terpolymer is replaced by amination groups, said reacting being carried out at a temperature in the range of about 80° C. to about 200° C. and for a period of from 3 to 100 hours.
Claim 11
Dependent Claim 39 words
A method according to claim 8 wherein said chlorinating agent is chlorine and said reacting is at a temperature in the range of about 135° C. to about 180° C. and for a period of 5 to 20 hours.

References Cited (Backward Citations)

US3445387A Cited
US3524826A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-27 1980-12-27 1981-06-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-27 1984-12-27 1985-06-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-27 1988-12-27 1989-06-28 $7700.00 Window Closed / Lapsed

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