Transparent graft copolymers based on acrylate soft phases

Patent metadata

Field	Value
Publication number	US-10858470-B2
Application number	US-201716325440-A
Country	US
Kind code	B2
Filing date	Aug 9, 2017
Priority date	Aug 17, 2016
Publication date	Dec 8, 2020
Grant date	Dec 8, 2020

Abstract

The invention relates to graft copolymers—based on non-cross-linked acrylate soft phases from which styrenic monomers are grafted—with a defined micro-structure, having a high transparency, toughness and weather resistance (UV-stability), a process for their preparation and their use, and also to polymer blends comprising said graft copolymers and styrenic polymers, and shaped articles produced therefrom and their use.

First claim

The invention claimed is:

1. A graft copolymer B, built up from:
(B1) 15 to 45 wt.-%, based on the graft copolymer B, of a non-cross-linked graft substrate polymer B1 having a glass transition temperature T G below 25° C. (DSC, heating rate: 5K/min), consisting of polymerized units derived from monomers B11, B12, and optionally B13:
(B11) from 95 to 99.5 wt.-%, based on the total weight of B11, B12, and B13, of at least one C 1 -C 10 -alkyl acrylate;
(B12) from 0.5 to 5 wt.-%, based on the total weight of B11, B12 and B13, of at least one monomer (=(meth)acrylate) of the formula (I)
H 2 C═CR 1 —CO—O—R 2 —X  (I),

wherein R 1 ═H or CH 3 , R 2 ═C 1 -C 4 -alkanediyl, X═NH 2 , OH or

and (B13) from 0 to 4.5 wt.-%, based on the total weight of B11, B12, and B13, of at least one other copolymerizable, monoethylenically unsaturated monomer; and
(B2) 55 to 85 wt.-%, based on the graft copolymer B, of at least one polymer B2 having a glass transition temperature T G above 25° C., grafted (in the form of branches) from the graft substrate polymer (B1), where polymer B2 consists of polymerized units derived from monomers B21 and optional comonomers B22:
(B21) from 65 to 100 wt.-% of at least one vinylaromatic monomer and/or of a C 1 -C 8 -alkyl-(meth)acrylate; and
(B22) from 0 to 35 wt.-% of at least one other monofunctional comonomer;

where components B1 and B2 give 100 wt.-% in total, and
wherein
the graft substrate polymer B1 has a gel content (non-soluble fraction in toluene) below 5 wt.-%, based on the total amount of B1;
the polymerized units derived from monomer B12 are chemically modified by moieties of the formula (II) H 2 C═CR 1 —CO— (II) (R 1 ═H or CH 3 ) which are covalently bound to the functional groups X; and
the double bond of the moiety of formula (II) is the active site from which polymerized units derived from monomer B21 and optionally comonomer B22 are grafted.

2. The graft copolymer B according to claim 1 having a transmittance T of at least 75% (determined according to ASTM D1003) and a haze coefficient below 10% (determined according to ASTM D1003-95).

3. The graft copolymer B according to claim 1 , wherein monomer B11 is ethyl acrylate, 2-ethylhexyl acrylate, n-butyl acrylate, or mixtures thereof.

4. The graft copolymer B according to claim 1 , wherein monomer B12 of the formula (I) is hydroxyethyl acrylate (HEA), glycidyl methacrylate (GMA), (2-hydroxyethyl) methacrylate (HEMA), or hydroxypropylmethacrylate.

5. The graft copolymer B according to claim 1 , wherein monomer B21 is styrene, α-methylstyrene, or a mixture of styrene or α-methylstyrene with methyl methacrylate.

6. The graft copolymer B according to claim 1 , wherein comonomer B22 is maleic anhydride or acrylonitrile.

7. The graft copolymer B according to claim 1 , wherein polymer B2 has been built up from styrene, or from a mixture consisting of 65 to 85 wt.-% styrene and 15 to 35 wt.-% acrylonitrile, maleic anhydride, or methyl methacrylate.

8. The graft copolymer B according to claim 1 , wherein monomer B13 is not present.

9. The graft copolymer B according to claim 1 built up from:
(B1) 20 to 40 wt.-% of graft substrate polymer B1; and
(B2) 60 to 80 wt.-% of polymer B2.

10. A process for the preparation of the graft copolymer B according to claim 1 , which comprises the following steps:
(i) free radical aqueous emulsion polymerization of monomers B11, B12, and optionally B13 in presence of an initiator PI-1;
(ii) chemical modification of graft substrate polymer B1 obtained in step (i) by reaction of the functional groups X with (meth)acrylic acid, its acid chloride, its acid anhydride, or its salts in presence of a base and a polymerization inhibitor;
(iii) grafting monomer B21 and optional comonomer B22 from graft substrate polymer B1 obtained in step (ii) by free radical emulsion or solution polymerization in presence of an initiator PI-2;

where the initiators PI-1 and PI-2 can be the same or different compounds, and
wherein
step i) is performed in the presence of 0.85 to 2 wt.-% of at least one chain transfer agent, based on the total amount of monomers B11, B12, and B13;
step ii) is performed in aqueous emulsion or in an organic solvent, the amount of graft substrate polymer B1 is 20 to 75 wt.-%, based on the total reaction medium, and the amount of (meth)acrylic acid or its said derivatives is 10 to 20 wt.-%, relative to B1; and
in step iii):
the amount of initiator PI-2 is 0.1 to 3 wt. % relative to the total content of monomers B21 and B22; and
monomer B21 and, if present, comonomer B22, and optionally the initiator PI-2 are fed continuously to the reaction mixture over 8 to 20 hours at a temperature of from 50 to 100° C.

11. The process according to claim 10 , wherein in step i) the chain transfer agent is added stepwise in two or more portions.

12. The process according to claim 10 , wherein in step iii) the monomer, and optional initiator, feed is over 10 to 18 hours.

13. A process for the preparation of the graft copolymer B according to claim 1 , which comprises the following steps:
(i-s) free radical solution polymerization of monomers B11, B12, and optionally B13 in presence of an initiator PI-1;
(ii) chemical modification of graft substrate polymer B1 obtained in step (i) by reaction of the functional groups X with (meth)acrylic acid, its acid chloride, its acid anhydride, or its salts in presence of a base and a polymerization inhibitor;
(iii) grafting monomer B21 and optional comonomer B22 from graft substrate polymer B1 obtained in step (ii) by free radical solution polymerization in presence of an initiator PI-2;

where the initiators PI-1 and PI-2 can be the same or different compounds, and
wherein
step i) is performed in the presence of 0.85 to 2 wt.-% of at least one chain transfer agent, based on the total amount of monomers B11, B12, and B13;
step ii) is performed in aqueous emulsion or in an organic solvent, the amount of graft substrate polymer B1 is 20 to 75 wt.-%, based on the total reaction medium, and the amount of (meth)acrylic acid or its said derivatives is 10 to 20 wt.-%, relative to B1; and
in step iii):
the amount of initiator PI-2 is 0.1 to 3 wt.-% relative to the total content of monomers B21 and B22; and
monomer B21 and, if present, comonomer B22, and optionally the initiator PI-2 are fed continuously to the reaction mixture over 8 to 20 hours at a temperature of from 50 to 100° C.,

wherein in all steps (i-s), (ii), and (iii) an organic solvent is used as reaction medium.

14. A graft copolymer B obtained by the process according to claim 10 .

15. A molding composition comprising at least one graft copolymer B according to claim 1 , and optionally additives and/or auxiliaries C.

16. The molding composition according to claim 15 , further comprising at least one thermoplastic polymer A having a glass transition temperature above 25° C.

17. The molding composition according to claim 16 , wherein the thermoplastic polymer A is selected from standard polystyrene (GPPS, homopolystyrene), styrene-acrylonitrile copolymers (SAN), α-methylstyrene-acrylonitrile copolymers (AMSAN), styrene-maleic anhydride copolymers (SMSA), and styrene-methyl methacrylate copolymers (SMMA).

18. The molding composition according to claim 16 , comprising:
5 to 60 wt.-% of at least one graft copolymer B,
30 to 95 wt.-% of at least one thermoplastic polymer A, and
0 to

Assignees

• Ineos Styrolution Group Gmbh

Inventors

• Niessner Norbert
• Schulz Tobias
• Carstensen Oliver
• Knoll Konrad
• Doering Manfred
• Schoenberger Frank
• Fage Julien

Classifications

• C08F220/1802

  C2-(meth)acrylate, e.g. ethyl (meth)acrylate · CPC title

• C08F220/1804

  C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate · CPC title

• C08F220/20

  of polyhydric alcohols or phenols {, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate} · CPC title

• C08F8/14

  Esterification · CPC title

• C08F2/22

  Emulsion polymerisation · CPC title