IP Library Patent Application 12288360
Patent Application
App. No. 12/288,360

Mar resistant thermoplastic alloys

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Quick Facts
Patent No.
US None
App. No.
12/288,360
Filed
Oct 20, 2008
Art Unit
1762
USPC
524/585
Abstract

Methods and compositions of matter that improve the specular gloss retention and mar resistance of articles made from amorphous and semi-crystalline polymers by employing a combination of polydialkylsiloxane and at least one additive selected from the group of organic amines, organic acids, triazynyl compounds, inorganic salts or bases, grafted or copolymerized polyolefins, and aluminum hydroxide.

Claims (31)

1 . A method for forming a thermoplastic alloy that upon forming into an article exhibits 1) an initial specular gloss of at least about 70 measured at a 20° glossmeter geometry, 2) a specular gloss retention of at least about 65% of said initial specular gloss as measured by a crockmeter mar test, and substantial resistance to visible marring, said method comprising preparing a blend consisting essentially of the components

A) from about 60 wt. % to about 95 wt. % of at least one polymer selected from the group consisting of amorphous polymer and semi-crystalline polymer,

B) from about 0.5 wt. % to about 3 wt. % polydialkylsiloxane, and

C) from about 0.2 wt. % to about 0.95 wt. % of at least one material selected from the group consisting of the subgroups 1) at least one organic amine having a boiling point of at least about 150° C. and a molecular weight of from about 110 to about 5,000, 2) at least one organic acid having a boiling point of at least about 150° C. and a molecular weight of from about 120 to about 3,000, 3) at least one triazynyl compound having a boiling point of at least about 150° C. and a molecular weight of from about 200 to about 5,000, 4) at least one alkali metal halide, 5) at least one alkaline earth metal compound, 6) at least one polyolefin backbone which is at least one of grafted or copolymerized with at least one of maleic anhydride, acrylic acid, and acrylic amide, and 7) aluminum hydroxide, all wt. % being based on the total weight of said alloy.

2 . The method of claim 1 wherein said component A) is selected from the group consisting of a homopolymer of propylene, a copolymer of at least 50 wt. % propylene and at least one other C2 to C20 alpha-olefin, acrylonitrile-butadiene-styrene copolymer, styrene-acrylonitrile copolymer, styrene-maleic anhydride copolymer, polymethylmethacrylate, poly(aromatic carbonate)s, and mixtures of two or more thereof.

3 . The method of claim 1 wherein at least one compatibilizer is added in an amount up to about 30 wt. %, said compatibilizer being selected from the group consisting of styrene-butadiene-styrene, styrene-ethylene/butylene-styrene, styrene-ethylene/propylene-styrene, a copolymer of ethylene and at least one other C3 to C20 alpha-olefin, ethylene propylene ethylidene norbornene, and mixtures of two or more thereof.

4 . The method of claim 1 wherein said component B) is a polydimethylsiloxane having the repeating formula —[—Si(CH 3 ) 2 —O—] n —, and a molecular weight of from about 1,000 to about 1,000,000.

5 . The method of claim 1 wherein said subgroups 1) through 7) of material C) are selected from the group consisting of 1) piperidinyl amine, melamine; 2) organic acids having from 4 to 20 carbon atoms per molecule; 3) triazine; 4) alkali metal halides; 5) alkaline earth metal bases, alkaline earth metal salts; 6) grafted polyolefin backbones of an olefin having from 2 to 12 carbon atoms per molecule; and 7) aluminum hydroxide.

6 . The method of claim 1 wherein said subgroups 1) through 7) of material C) are selected from the group consisting of a) bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; b) poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); c) decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl)ester; d) poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; e) a mixture of a), b), and 2-(2′-hydroxy-3′,5′-ditert-butylphenyl)-benzotriazole; f) a mixture of a), b), and 2-hydroxyl-4-n-octoxybenzophenone; g) melamine; h) fumaric acid; i) succinic acid; j) triazine; k) sodium chloride; l) sodium bromide; m) sodium iodide; n) potassium chloride; o) potassium bromide; p) potassium iodide; q) calcium carbonate; r) magnesium carbonate; s) calcium hydroxide; t) magnesium hydroxide; u) aluminum hydroxide; and v) at least one polyolefin backbone of an olefin having from 2 to 12 carbon atoms per molecule which is at least one of grafted or copolymerized with from about 0.5 wt. % to about 10 wt. % based on the total weight of said polyolefin with at least one of maleic anhydride, acrylic acid and acrylic amide.

7 . The method of claim 1 wherein said material C) is at least one material selected from the group consisting of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl) ester; poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-(2′-hydroxy-3′,5′-ditert-butyl phenyl)-benzotriazole; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-hydroxyl-4-n-octoxybenzophenone; melamine; fumaric acid; succinic acid; triazine; sodium chloride; and calcium carbonate.

8 . The method of claim 1 wherein said alloy is formed by mixing components A) through C) at a temperature of from about 165° C. to about 250° C.

9 . The method of claim 1 wherein at least one conventional additive is mixed into said alloy, and the amount of component C) employed in said alloy is in addition to the amount of said conventional additive mixed into said alloy.

10 . A composition consisting essentially of the components

A) from about 60 wt. % to about 95 wt. % of at least one polymer selected from the group consisting of amorphous polymer and semi-crystalline polymer,

B) from about 0.5 wt. % to about 3 wt. % polydialkylsiloxane, and

C) from about 0.2 wt. % to about 0.95 wt. % of at least one material selected from the group consisting of the subgroups 1) at least one organic amine having a boiling point of at least about 150° C. and a molecular weight of from about 110 to about 5,000, 2) at least one organic acid having a boiling point of at least about 150° C. and a molecular weight of from about 120 to about 3,000, 3) at least one triazynyl compound having a boiling point of at least about 150° C. and a molecular weight of from about 200 to about 5,000, 4) at least one alkali metal halide, 5) at least one alkaline earth metal compound, 6) at least one polyolefin backbone which is at least one of grafted or copolymerized with at least one of maleic anhydride, acrylic acid, and acrylic amide, and 7) aluminum hydroxide, all wt. % being based on the total weight of said alloy.

11 . The composition of claim 10 wherein said component A) is selected from the group consisting of a homopolymer of propylene, copolymer of at least 50 wt. % propylene and at least one other C2 to C20 alpha-olefin, acrylonitrile-butadiene-styrene copolymer, styrene-acrylonitrile copolymer, styrene-maleic anhydride copolymer, polymethylmethacrylate, poly(aromatic carbonate)s, and mixtures of two or more thereof.

12 . The composition of claim 10 wherein at least one compatibilizer is added in an amount up to about 30 wt. %, said compatibilizer being selected from the group consisting of styrene-butadiene-styrene, styrene-ethylene/butylene-styrene, styrene-ethylene/propylene-styrene, a copolymer of ethylene and at least one other C3 to C20 alpha-olefin, ethylene propylene ethylidene norbornene, and mixtures of two or more thereof.

13 . The composition of claim 10 wherein said component B) is a polydimethylsiloxane having the formula —[—Si(CH 3 ) 2 —O—] n —, and a molecular weight of from about 1,000 to about 1,000,000.

14 . The composition of claim 10 wherein said subgroups 1) through 7) of material C) are selected from the group consisting of 1) piperidinyl amine, melamine; 2) organic acids having from 4 to 20 carbon atoms per molecule; 3) triazine; 4) alkali metal halides; 5) alkaline earth metal bases, alkaline earth metal salts; 6) grafted polyolefin backbones of an olefin having from 2 to 12 carbon atoms per molecule; and 7) aluminum hydroxide.

15 . The composition of claim 10 wherein said subgroups 1) through 7) of material C) are selected from the group consisting of a) bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; b) poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); c) decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl)ester; d) poly[[6-[(1,1,3,3-tetramethylbutyl )amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; e) a mixture of a), b), and 2-(2′-hydroxy-3′,5′-ditert-butylphenyl)-benzotriazole; f) a mixture of a), b), and 2-hydroxyl-4-n-octoxybenzophenone; g) melamine; h) fumaric acid; i) succinic acid; j) triazine; k) sodium chloride; l) sodium bromide; m) sodium iodide; n) potassium chloride; o) potassium bromide; p) potassium iodide; q) calcium carbonate; r) magnesium carbonate; s) calcium hydroxide; t) magnesium hydroxide; u) aluminum hydroxide; and v) at least one polyolefin backbone of an olefin having from 2 to 12 carbon atoms per molecule grafted or copolymerized with from about 0.5 wt. % to about 10 wt. % based on the total weight of said polyolefin with at least one of maleic anhydride, acrylic acid and acrylic amide.

16 . The composition of claim 10 wherein said material C) is at least one material selected from the group consisting of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl)ester; poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-(2′-hydroxy-3′,5′-ditert-butylphenyl)-benzotriazole; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-hydroxyl-4-n-octoxybenzophenone; melamine; fumaric acid; succinic acid; triazine; sodium chloride; and calcium carbonate.

17 . The composition of claim 10 wherein at least one conventional additive is present in said alloy, and the amount of component C) present in said alloy is in addition to the amount of said conventional additive present.

18 . A molded article of the composition of claim 10 .

19 . An extruded article of the composition of claim 10 .

20 . A thermoplastic additive consisting essentially of from about 0.3 wt. % to about 3 wt. % polydialkylsiloxane, the remainder being at least one material selected from the group consisting of 1) at least one organic amine having a boiling point of at least about 150° C. and a molecular weight of from about 110 to about 5,000; 2) at least one organic acid having a boiling point of at least about 150° C. and a molecular weight of from about 120 to about 3,000; 3) at least one triazynyl compound having a boiling point of at least about 150 C. and a molecular weight of from about 200 to about 5,000; 4) at least one alkali metal halide; 5) at least one alkaline earth metal compound; 6) at least one polyolefin backbone which is at least one of grafted or copolymerized with at least one of maleic anhydride, acrylic acid, and acrylic amide; and 7) aluminum hydroxide, all wt. % being based on the total weight of said additive.

21 . The additive of claim 20 wherein said polydialkylsiloxane is a polydimethylsiloxane having the formula —[—Si(CH 3 ) 2 —O—] n —, and a molecular weight of from about 1,000 to about 1,000,000.

22 . The method of claim 20 wherein said at least one material is selected from the group consisting of piperidinyl amine, melamine; organic acids having from 4 to 20 carbon atoms per molecule; triazine; alkali metal halides; alkaline earth metal bases, alkaline earth metal salts; grafted polyolefin backbones of an olefin having from 2 to 12 carbon atoms per molecule; and aluminum hydroxide.

23 . The additive of claim 20 wherein said at least one material is selected from the group consisting of a) bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; b) poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); c)decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl) ester; d) poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; e) a mixture of a), b), and 2-(2′-hydroxy-3′,5′-ditert-butylphenyl)-benzotriazole; f) a mixture of a), b), and 2-hydroxyl-4-n-octoxybenzophenone; g) melamine; h) fumaric acid; i) succinic acid; j) triazine; k) sodium chloride; l) sodium bromide; m) sodium iodide; n) potassium chloride; o) potassium bromide; p) potassium iodide; q) calcium carbonate; r) magnesium carbonate; s) calcium hydroxide; t) magnesium hydroxide; u) aluminum hydroxide; and v) at least one polyolefin backbone of an olefin having from 2 to 12 carbon atoms per molecule which is at least one of grafted or copolymerized with from about 0.5 wt. % to about 10 wt. % based on the total weight of said polyolefin with at least one of maleic anhydride, acrylic acid and acrylic amide.

24 . The additive of claim 20 wherein said at least one material is selected from the group consisting of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate; poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid); decanedioic acid bis(2,2,6,6-tetramethyl-1-(octyloxy)-4-piperidinyl)ester; poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-(2′-hydroxy-3′,5′-ditert-butylphenyl)-benzotriazole; a mixture of bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate, poly(4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol-alt-1,4-butanedioic acid), and 2-hydroxyl-4-n-octoxybenzophenone; melamine; fumaric acid; succinic acid; triazine; sodium chloride; and calcium carbonate.

25 . A method for making the additive of claim 20 wherein the components of said additive are mixed at a temperature of from about 165° C. to about 250° C.

Assignments (14)
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032112/0786 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 22, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032112/0863 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: CITIBANK, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0644 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0684 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: BANK OF AMERICA, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0730 →
SECURITY AGREEMENT Recorded May 19, 2010
From: EQUISTAR CHEMICALS, LP
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0655 →
SECURITY AGREEMENT Recorded May 18, 2010
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0861 →
SECURITY AGREEMENT Recorded May 7, 2010
From: EQUISTAR CHEMICALS. LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024351/0001 →
SECURITY AGREEMENT Recorded May 6, 2010
From: EQUISTAR CHEMICALS, LP
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0443 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0186 →
RELEASE OF SECURITY INTEREST Recorded May 4, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024329/0535 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: EQUISTAR CHEMICALS, LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0687 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022678/0860 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2008
From: CAI, KEVIN
To: LYONDELLBASELL ADVANCED POLYOLEFINS USA INC.
Reel/Frame 021775/0988 →