IP Library Granted Patent US 12,359,010
Granted Patent B2
US 12,359,010 · App. 18/616,251 · Granted Jul 15, 2025

Polymer latex for dip-molding applications

Inventors: Andrew Kells (Kuala Lumpur, MY); Sören Butz (Dülmen, DE); Alexandra Abele (Dülmen, DE); Peter L. Shaw (Bishop's Stortford, GB); Brian Saunders (Sale, GB); Gareth Simpson (Sawston, GB)
Assignee: Synthomer Sdn. Bhd.
C08F265/04B29C41/003B29C41/14C08F293/005C09D5/022C09D151/003C09D153/02B29K2105/0064B29L2031/4864C08F220/1804C08F2438/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,359,010
App. No.
18/616,251
Granted
Jul 15, 2025
Kind
B2
Abstract

The present invention relates to a polymer latex for dip-molding applications obtainable by free-radical emulsion polymerization of a mixture of ethylenically unsaturated monomers comprising at least one conjugated diene and at least one ethylenically unsaturated nitrile compound in an aqueous medium in presence of seed latex particles having a glass transition temperature (mid point temperature Tmg) measured by DSC according to ASTM D3418-03 of −50° C. to 50° C. wherein the seed latex particles do not contain structural units derived from ethylenically unsaturated nitrile compounds, to a method of preparing said polymer latex, to articles made by using said polymer latex and to a method for preparing dip-molded articles from said polymer latex.

Claims (37)

1. A polymer latex for dip-molding applications obtained by free-radical emulsion polymerization of a mixture of ethylenically unsaturated monomers comprising at least one conjugated diene and at least one ethylenically unsaturated nitrile compound, wherein the unsaturated nitrile is present in amounts of at least 22 wt.-% based on the total weight of the ethylenically unsaturated monomers in an aqueous medium in presence of seed latex particles having a glass transition temperature (mid point temperature Tmg) measured by DSC according to ASTM D3418-03 of −40° C. to 50° C. wherein the seed latex particles do not contain structural units derived from ethylenically unsaturated nitrile compounds, wherein the seed latex particles comprise structural units derived from 80 to 99.95 wt.-% of alkyl esters of ethylenically unsaturated acids, and 0.05 to 10 wt.-% of ethylenically unsaturated acids, based on the total weight of monomers constituting the seed particles, and wherein a z-average particle size measured with a Malvern zetasizer nano S (ZEN 1600) using dynamic light scattering of the seed latex particles is 10 to 80 nm.

2. The polymer latex of claim 1 , wherein the seed latex particles comprise structural units derived from monomers selected from:

vinyl aromatic monomers;

alkyl esters of ethylenically unsaturated acids;

hydroxyalkyl esters of ethylenically unsaturated acids,

amides of ethylenically unsaturated acids;

ethylenically unsaturated acids;

vinyl carboxylates;

conjugated dienes;

monomers having at least two ethylenically unsaturated groups; and

combinations thereof.

3. The polymer latex of claim 1 , wherein the Tmg of the seed latex particles is −40° C. to 40° C.

4. The polymer latex of claim 1 , wherein the seed latex particles are present in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of total ethylenically unsaturated monomers employed in the emulsion polymerization.

5. The polymer latex of claim 1 , wherein the z-average particle size measured with a Malvern zetasizer nano S (ZEN 1600) using dynamic light scattering of the seed latex particles is 15 to 80 nm.

6. The polymer latex of claim 1 , wherein

the conjugated diene is selected from butadiene, isoprene and combinations thereof;

the ethylenically unsaturated nitrile compound is selected from (meth)acrylonitrile, alpha-cyanoethyl acrylonitrile, fumaronitrile, and combinations thereof; and

the mixture of ethylenically unsaturated monomers optionally comprises ethylenically unsaturated monomers selected from:

vinyl aromatic monomers;

alkyl esters of ethylenically unsaturated acids;

hydroxyalkyl esters of ethylenically unsaturated acids;

amides of ethylenically unsaturated acids;

vinyl carboxylates; and

combinations thereof.

7. The polymer latex of claim 1 , wherein the ethylenically unsaturated monomers are selected from:

15 to 99 wt.-% of conjugated dienes;

22 to 80 wt.-% of monomers selected from ethylenically unsaturated nitrile compounds;

0 to 40 wt.-% of vinyl aromatic monomers;

0 to 25 wt.-% of C 1 to C 8 alkyl (meth)acrylate;

0 to 10 wt.-% of ethylenically unsaturated acids;

0 to 10 wt.-% of ethylenically unsaturated compounds bearing silane, sulfonate, sulfonic acid, amide and/or N-methylolamide groups,

the weight percentages being based on the total monomers employed in the emulsion polymerization.

8. The polymer latex of claim 2 , wherein the alkyl esters of ethylenically unsaturated acids comprise a combination of 2 or more alkyl esters of ethylenically unsaturated acids.

9. A compounded latex composition suitable for the production of dip-molded

articles comprising the polymer latex according to claim 1 and optionally adjuvants selected from sulfur, accelerators for sulfur vulcanization, crosslinkers, polyvalent cations, and combinations thereof.

10. An article made using the polymer latex according to claim 1 .

11. The article of claim 10 , being selected from surgical gloves, examination gloves, condoms, catheters, industrial gloves, textile-supported gloves and household gloves.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2024
From: KELLS, ANDREW; BUTZ, SÖREN; ABELE, ALEXANDRA; SHAW, PETER; SAUNDERS, BRIAN; SIMPSON, GARETH
To: SYNTHOMER SDN. BHD.
Reel/Frame 066897/0133 →
Continuity (2)
Continuation 16086775
Related Publication 20240343851A1 · Oct 17, 2024
References Cited (25)
US 4525519A · Leising · 1985 [cited by applicant]
US 5084514A · Szczechura et al. · 1992 [cited by applicant]
US 5750618A · Vogt et al. · 1998 [cited by applicant]
US 6492446B1 · Kajiwara et al. · 2002 [cited by applicant]
US 6870019B2 · Kajiwara et al. · 2005 [cited by applicant]
US 8557934B2 · Takeno et al. · 2013 [cited by applicant]
US 10982075B2 · Wei et al. · 2021 [cited by applicant]
US 11965046B2 · Kells · 2024 [cited by examiner]
US 20030138579A1 · Savoca et al. · 2003 [cited by applicant]
US 20030175500A1 · Mukherjee et al. · 2003 [cited by applicant]
US 20060052513A1 · Butz et al. · 2006 [cited by applicant]
EP 0486183A1 · 1992 [cited by applicant]
EP 0792891A1 · 1997 [cited by applicant]
EP 1063258A2 · 2000 [cited by applicant]
EP 1215236A2 · 2002 [cited by applicant]
EP 2298823A1 · 2011 [cited by applicant]
JP H06248030A · 1994 [cited by applicant]
JP H0848705A · 1996 [cited by applicant]
JP 2001310976A · 2001 [cited by examiner]
JP 2002220406A · 2002 [cited by applicant]
JP 2005133009A · 2005 [cited by applicant]
JP 2005200559A · 2005 [cited by applicant]
JP 3920633B2 · 2007 [cited by applicant]
WO 0011980 · 2000 [cited by applicant]
“Standard Test Method for Transition Temperatures of Ploymers By Differential Scanning Calorimetry,” D 3418-03, 2003, ASTM International, West Conshohocken, PA. [cited by applicant]