IP Library Granted Patent US 10,731,097
Granted Patent B2
US 10,731,097 · App. 16/119,878 · Granted Aug 4, 2020

Viscosity index improvers with defined molecular weight distributions

Inventors: Katrin Schöller (Darmstadt, DE); Sarah Lippert (Darmstadt, DE); Wolfgang Tschepat (Darmstadt, DE); Klaus Schimossek (Bensheim, DE)
Assignee: Evonik Operations GmbH
C10M145/14C08C19/28C08F220/18C08F290/048C08F220/1804C08L2203/40C10M2209/084C10N2020/02C10N2020/04C10N2030/02C10N2030/54C10N2030/68C10N2030/74C10N2040/25C10N2070/00
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Quick Facts
Patent No.
US 10,731,097
App. No.
16/119,878
Granted
Aug 4, 2020
Kind
B2
Abstract

Polyalkyl(meth)acrylate based comb polymers with weight-average molecular weights of 700,000 g/mol or greater and number-average molecular weights of 130,000 g/mol or greater can be used to improve the high temperature-high shear performance of lubricant compositions, especially of engine oil (EO) compositions. These polymers can be obtained in a reaction mixture comprising monomers, a dilution oil, and an initiator. The resulting lubricant compositions can have improved kinematic viscosity and high temperature high shear performance.

Claims (65)

1. A polyalkyl(meth)acrylate based comb polymer, consisting of:

(a) 10 to 25% by weight of an ester of (meth)acrylic acid and a hydroxylated hydrogenated polybutadiene;

(b) 0% to 5% by weight of at least one C 4-18 alkyl acrylate;

(c) 0% to 0.3% by weight of methyl methacrylate;

(d) 60% to 75% by weight of n-butyl methacrylate;

(e) 5% to 20% by weight of at least one C 10-30 alkyl (meth)acrylate; and

(f) 0% to 2% by weight of at least one styrene monomer,

wherein the polyalkyl(meth)acrylate based comb polymer has a weight-average molecular weight M w of 700,000 g/mol or greater and a number-average molecular weight M n of 130,000 g/mol or greater, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard.

2. The polyalkyl(meth)acrylate based comb polymer according to claim 1 , wherein the weight-average molecular weight M w is from 700,000 to 2,000,000 g/mol and the number-average molecular weight M n is from 130,000 to 300,000 g/mol, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard.

3. The polyalkyl(meth)acrylate based comb polymer according to claim 1 , having a value P of 1.5 or lower:

P

=

M

w

-

0.8

M

n

×

10

10

1.5

.

4. A method of increasing KV 100 and in parallel decreasing HTHS 100 and HTHS 80 of a lubricating oil composition, the method comprising adding the polyalkyl(meth)acrylate based comb polymer according to claim 1 to a lubricating oil composition in need thereof.

5. An additive composition, comprising:

(A) 60 to 80% by weight of a base oil, and

(B) 20 to 40% by weight of a polyalkyl(meth)acrylate based comb polymer, which has a weight-average molecular weight M w of 700,000 g/mol or greater and a number-average molecular weight M n of 130,000 g/mol or greater, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard,

wherein the polyalkyl(meth)acrylate based comb polymer (B) consists of the following monomers:

(a) 10 to 25% by weight of an ester of (meth)acrylic acid and a hydroxylated hydrogenated polybutadiene;

(b) 0% to 5% by weight of at least one C 4-18 alkyl acrylate;

(c) 0% to 0.3% by weight of methyl methacrylate;

(d) 60% to 75% by weight of n-butyl methacrylate;

(e) 5% to 20% by weight of at least one C 10-30 alkyl (meth)acrylate; and

(f) 0% to 2% by weight of at least one styrene monomer.

6. The additive composition according to claim 5 , wherein the weight-average molecular weight M w of component (B) is from 700,000 to 2,000,000 g/mol and the number-average molecular weight M n is from 130,000 to 300,000 g/mol, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard.

7. A method of increasing KV 100 and in parallel decreasing HTHS 100 of a lubricating oil composition, the method comprising adding the additive composition according to claim 5 to a lubricating oil composition in need thereof.

8. A lubricating oil composition, comprising:

(A) 80 to 99.5% by weight of a base oil;

(B) 0.5 to 5% by weight of a polyalkyl(meth)acrylate based comb polymer, which has a weight-average molecular weight M w of 700,000 g/mol or greater and a number-average molecular weight M n of 130,000 g/mol or greater, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard; and

(C) 0 to 15% by weight of one or more further additives,

wherein component (B) consists of:

(a) 10 to 25% by weight of an ester of (meth)acrylic acid and a hydroxylated hydrogenated polybutadiene;

(b) 0% to 5% by weight of at least one C 4-18 alkyl acrylate;

(c) 0% to 0.3% by weight of methyl methacrylate;

(d) 60% to 75% by weight of n-butyl methacrylate;

(e) 5% to 20% by weight of at least one C 10-30 alkyl (meth)acrylate; and

(f) 0% to 2% by weight of at least one styrene monomer.

9. The lubricating oil composition according to claim 8 , wherein the weight-average molecular weight M w of component (B) is from 700,000 to 2,000,000 g/mol and the number-average molecular weight M n is from 130,000 to 300,000 g/mol, determined by size exclusion chromatography (SEC) using a polymethylmethacrylate standard.

10. The lubricating oil composition according to claim 8 , wherein component (C) is at least one selected from the group consisting of conventional VI improvers, dispersants, defoamers, detergents, antioxidants, pour point depressants, antiwear additives, extreme pressure additives, friction modifiers, anticorrosion additives, dyes and mixtures thereof.

11. A process for preparing the polyalkyl(meth)acrylate based comb polymer according to claim 1 , the process comprising:

(a) preparing a reaction mixture comprising monomers and a first dilution oil, wherein the monomers are present in an amount of 40 to 65% by weight;

(b) heating 50% of the reaction mixture prepared under (a) to a first temperature of from 80 to 120° C.;

(c) adding 0.05 to 0.1%, based on the total amount of the monomers, of a first initiator to the reaction mixture as prepared under (b), the first initiator having a half-life T 1/2 of from 100 to 200 minutes, at the first temperature according to (b);

(d) adding a further amount of the reaction mixture prepared under and further 0.05 to 0.1% of the first initiator during a time of from 2 to 4 hours;

(e) maintaining the reaction mixture prepared under (d) for a time of 0.5 to 3 hours at the first temperature;

(f) diluting the reaction mixture prepared under (e) during a time of 0.5 to 3 hours to 30% with a second dilution oil, which can be the same or different than the first dilution oil, comprising a further amount of the first initiator;

(g) optionally adding further amount of the first initiator or a second initiator, which can be the same as or different than the first initiator, to the reaction mixture prepared under (e) and maintaining for at least 2 hours; and

(h) diluting the reaction mixture prepared under (g) by addition of the first dilution oil or the second dilution oil.

12. The process according to claim 11 , wherein the first and second initiators are the same or different and are each independently selected from the group consisting of azo initiators, and peroxy compounds.

13. The process according to claim 11 , wherein the first initiator is 1,1-di-tert-butylperoxy-3,3,5-trimethylcyclohexan and the second initiator is tert-butylperoxy 2-ethylhexanoate or 1,1-di-tert-butylperoxy-3,3,5-trimethylcyclohexan.

14. The process according to claim 11 , wherein the first and second dilution oils are the same or different and are each independently selected from the group consisting of API Group I, II, III, IV, V and mixtures thereof.

15. The process according to claim 12 , wherein the first and second initiators are each independently at least one selected from the group consisting of azobis-isobutyronitrile (AIBN), 2,2′-azobis(2-methylbutyronitrile) (AMBN), 1,1-azobiscyclohexanecarbonitrile, methyl ethyl ketone peroxide, acetylacetone peroxide, dilauryl peroxide, tert-butyl per-2-ethylhexanoate, ketone peroxide, tert-butyl peroctoate, methyl isobutyl ketone peroxide, cyclohexanone peroxide, dibenzoyl peroxide, tert-butyl peroxybenzoate, tert-butyl peroxyisopropylcarbonate, 2,5-bis(2-ethylhexanoylperoxy)-2,5-dimethylhexane, tert-butyl peroxy-2-ethylhexanoate, tert-butyl peroxy-3,5,5-trimethylhexanoate, dicumyl peroxide, 1,1-bis(tert-butylperoxy)cyclohexane, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, cumyl hydroperoxide, tert-butyl hydroperoxide and bis(4-tert-butylcyclohexyl) peroxydicarbonate.

16. The lubricating oil composition of claim 8 , having a KV 100 of at least 6.9 mm 2 /s.

17. The lubricating oil composition of claim 8 , having a KV 100 of at least 6.9 mm 2 /s and an HTHS 80 of 6.0 mPas or less.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNOR PREVIOUSLY RECORDED ON REEL 051418 FRAME 0620. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER.. Recorded Jan 7, 2020
From: EVONIK OIL ADDITIVES GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 051496/0300 →
MERGER Recorded Jan 6, 2020
From: EVONIK OIL ADDITIVES
To: EVONIK DEGUSSA GMBH
Reel/Frame 051418/0620 →
CHANGE OF NAME Recorded Jan 6, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051418/0628 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2018
From: SCHÖLLER, KATRIN; LIPPERT, SARAH; TSCHEPAT, WOLFGANG; SCHIMOSSEK, KLAUS
To: EVONIK OIL ADDITIVES GMBH
Reel/Frame 047095/0650 →
Priority Claims (1)
EP 17189194 · Sep 4, 2017 · regional
Continuity (1)
Related Publication 20190071615A1 · Mar 7, 2019