IP Library Granted Patent US 9,688,804
Granted Patent B2
US 9,688,804 · App. 14/376,222 · Granted Jun 27, 2017

Polymeric beads, process and composition

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Quick Facts
Patent No.
US 9,688,804
App. No.
14/376,222
Granted
Jun 27, 2017
Kind
B2
Abstract

There are described a dispersion of polymeric beads where the beads comprise a copolymer composition comprising (preferably consisting essentially of): copolymers (and processes for making them) comprising (a) at least 8.5 wt-% preferably >=20 wt-% of a higher itaconate diester (preferably dibutyl itaconate—DBI); (b) less than 23 wt-% acid monomer but also sufficient to have an acid value less than 150 mg KOH/g of polymer, (c) optionally with less than 50 wt-% of other itaconate monomers, and (d) optionally less than 77 wt-% of other monomers not (a) to (c). The DBI may be biorenewable. A further embodiment is an aqueous suspension polymerization process for preparing vinyl polymer beads from olefinically unsaturated monomers and a free-radical initiator, where at least 10 wt-% of the monomer is DBI.

Claims (27)

1. A dispersion of polymeric beads, wherein the polymeric beads have an average diameter of between 50 μm and 1500 μm and comprise a copolymer containing styrene in an amount of less than 1.5% by weight of the copolymer, and wherein the copolymer comprises the following comonomers (a), (b), (c) and optionally (d):

(a) 24 to 70% by weight of one or more monomers represented by the Formula (1):

 where both R 1 and R 2 independently represent an optionally substituted hydrocarbo moiety having from 4 to 10 carbon atoms,

(b) at least one acid functional monomer in an amount from 0.5 to 15% by weight sufficient to a achieve an acid value of the resultant copolymer of 3 to 100 mg KOH per gram of copolymer,

(c) 0.01 to 10% by weight of one or more monomers represented by the Formula (2):

 in which X 1 and X 2 are both O and R 3 and/or R 4 independently represent an optionally substituted hydrocarbo moiety having from 1 to 3 carbon atoms, and

(d) optionally less than 75% by weight of monomer other than comonomers (a), (b) or (c) and does not contain styrene, butyl acrylate, 2-ethyl hexyl acrylate and/or mixtures thereof; wherein

the weight percentages or amounts of comonomers (a), (b), (c) and (d) are calculated as a proportion of the total amount of components (a)+(b)+(c)+(d) which totals 100%; and wherein

independently at least one of the comonomers (a), (b), (c) and/or (d) and/or the copolymer obtained from comonomers (a), (b), (c) and optionally (d) are biorenewable which is defined as comprising an amount of carbon-14 sufficient to produce a decay of at least about 1.5 disintegrations per minute per gram carbon (dpm/gC);

with the provisos that:

(i) when the copolymer is prepared by an emulsion polymerisation a chaser monomer is not used;

(ii) the copolymer is not prepared in the presence of a seed polymer comprising a poly(itaconate ester); and

(iii) the copolymer is not prepared in the presence of an initiator system comprising an organoborane amine complex.

2. The dispersion of polymeric beads as claimed in claim 1 , wherein component (a) comprises dibutyl itaconate.

3. The dispersion of polymeric beads as claimed in claim 1 , wherein;

comonomer (a) is present in an amount of from 30 to 65% by weight and is dibutyl itaconate;

comonomer (b) is present in an amount of up to 10% by weight and comprises an acid functional ethylenically unsaturated monomer and/or anhydride thereof; and

comonomer (c) is present in an amount of from 1 to 10% by weight and is dimethyl itaconate and/or diethyl itaconate; and

optional comonomer (d), if present, is present in an amount such that comonomers (a), (b), (c) and (d) total 100% by weight.

4. A process for preparing a dispersion of polymeric beads as claimed in claim 1 , the process comprising polymerising polymer precursors comprising comonomers (a), (b), (c) and optionally (d) to obtain a copolymer dispersed in a carrier.

5. The process as claimed in claim 4 , wherein the process comprises conducting suspension polymerisation of olefinically unsaturated monomers in the presence of a free radical initiator.

6. A dispersion obtained by the process according to claim 4 .

7. Polymeric beads obtained by isolation of the polymeric beads from the dispersion of polymeric beads as claimed in claim 1 .

8. A coating composition comprising a dispersion of the polymeric beads as claimed in claim 1 .

9. A substrate and/or article having coated thereon the coating composition of claim 8 , wherein the coating composition is optionally cured.

10. A method of preparing a coating composition which comprises mixing the dispersion of polymeric beads of claim 1 with components of a coating formulation.

11. A method for preparing a coated substrate and/or article comprising the steps of applying the coating composition of claim 8 to the substrate and/or article and optionally curing the coating composition in situ to form a cured coating thereon.

Assignments (4)
CHANGE OF CORPORATE ADDRESS Recorded Mar 30, 2022
From: COVESTRO (NETHERLANDS) B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 059546/0570 →
CHANGE OF NAME Recorded Jul 2, 2021
From: MS HOLDING B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 056756/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2021
From: DSM IP ASSETS B.V.
To: MS HOLDING B.V.
Reel/Frame 056726/0106 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2014
From: NABUURS, TIJS; OVERBEEK, GERARDUS CORNELIS; STUBBS, JEFFREY; GEBHARD, MATTHEW STEWART
To: DSM IP ASSETS B.V.
Reel/Frame 034571/0640 →