IP Library Granted Patent US 9,309,331
Granted Patent B2
US 9,309,331 · App. 14/431,166 · Granted Apr 12, 2016

Alkyl hydroxylamine compounds and their use for shortstopping free radical polymerizations

Inventors: Charles E. Coburn (Vernon Hills, IL); Mrunalini S. Dhamdhere (Vernon Hills, IL); Kaustubh Gupte (Mumbai, IN); Mahesh Sawant (Pune, IN)
Assignee: ANGUS CHEMICAL COMPANY
C08F2/42C08F36/06
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Quick Facts
Patent No.
US 9,309,331
App. No.
14/431,166
Granted
Apr 12, 2016
Kind
B2
Abstract

This invention provides a method for shortstopping free radical polymerization reactions using a shortstopping agent comprising at least two alkyl hydroxylamines (AHAs) selected from the group consisting of primary AHAs, a mixture of at least one of each of primary and secondary AHAs, and salts thereof. A method for producing elastomers using the aforesaid shortstopping agents is also provided.

Claims (30)

1. A method for terminating a free radical initiated emulsion polymerization reaction comprising: adding a shortstopping agent to an emulsion comprising at least one monomer to be polymerized, wherein

the shortstopping agent comprises at least two alkyl hydroxylamine compounds selected from the group consisting of

primary alkyl hydroxylamines, and

a mixture of at least one each of primary and secondary alkyl hydroxylamines,

with the proviso that N,N′-diethylhydroxylamine (DEHA) and isopropylhydroxylamine (IPHA) are absent.

2. The method of claim 1 , wherein the shortstopping agent comprises:

a. from 10% to 70% by weight of the at least two alkyl hydroxylamine compounds, based on the total weight of the shortstopping agent; and

b. from 30% to 90% by weight of a solvent, based on the total weight of the shortstopping agent.

3. The method of claim 1 , wherein said primary alkyl hydroxylamines are selected from the group consisting of: N-methylhydroxylamine (MHA), N-ethylhydroxylamine (EHA), N-propylhydroxylamine (PHA), N-tertiary-butylhydroxylamine (TBHA), and mixtures thereof.

4. The method of claim 1 , wherein said secondary alkyl hydroxylamines are selected from the group consisting of: N,N-dimethylhydroxylamine (DMHA), N,N-isopropylmethylhydroxylamine (IPMHA), and mixtures thereof.

5. The method of claim 1 , wherein the at least two alkyl hydroxylamines comprise a first primary alkyl hydroxylamine and a second primary alkyl hydroxylamine, wherein the first primary alkyl hydroxylamine and the second primary alkyl hydroxylamine are present in a weight ratio of from 10:90 to 65:35.

6. The method of claim 1 , wherein the at least two alkyl hydroxylamines comprise a mixture of at least one primary alkyl hydroxylamine and at least one secondary alkyl hydroxylamine, wherein the at least one primary alkyl hydroxylamine and the at least one secondary alkyl hydroxylamine are present in a weight ratio of from 90:10 to 50:50.

7. The method of claim 6 , wherein said mixture comprises greater than 50% by weight of the at least one primary alkyl hydroxylamine, based on the total weight of the primary and secondary alkyl hydroxylamines.

8. The method of claim 1 , wherein said shortstopping agent is added to said emulsion in an amount of from 0.01 to 0.25 parts per hundred parts of the at least one monomer.

9. A method for producing an elastomer comprising:

1) conducting in an emulsion, a free-radical emulsion polymerization of a latex comprising a conjugated diene, thereby producing polymerized material;

2) adding to the emulsion a shortstopping agent comprising at least two alkyl hydroxylamine compounds selected from the group consisting of:

(a) primary alkyl hydroxylamines, and

(b) a mixture of at least one of each of primary and secondary alkyl hydroxylamines,

with the proviso that N,N′-diethylhydroxylamine (DEHA) and isopropylhydroxylamine (IPHA) are absent; and

3) processing the polymerized material to form said elastomer.

10. The method of claim 9 , wherein said elastomer is a rubber selected from the group consisting of styrene-butadiene rubber, butadiene rubber, and acrylonitrile-butadiene rubber.

11. The method of claim 9 , wherein the free-radical emulsion polymerization is performed in a batch-wise mode.

12. The method of claim 9 , wherein the free-radical emulsion polymerization is performed in a continuous mode.

13. The method of claim 9 , wherein the free-radical emulsion polymerization has a temperature from 0° C. to 100° C.

14. The method of claim 1 , wherein the shortstopping agent comprises at least two or more primary alkyl hydroxylamines and at least one secondary alkyl hydroxylamine.

15. The method of claim 1 , wherein the shortstopping agent comprises at least one primary alkyl hydroxylamine and at least two or more secondary alkyl hydroxylamines.

16. The method of claim 1 , wherein said shortstopping agent is added to said emulsion in an amount of from 0.04 to 0.2 parts per hundred parts of the at least one monomer.

17. The method of claim 1 , wherein the at least two alkyl hydroxylamines comprise a mixture of at least one primary alkyl hydroxylamine and at least one secondary alkyl hydroxylamine, wherein the at least one primary alkyl hydroxylamine and the at least one secondary alkyl hydroxylamine are present in a weight ratio of from 90:10 to 60:40.

18. A method for terminating a free radical initiated emulsion polymerization reaction comprising: adding a shortstopping agent to an emulsion comprising at least one monomer to be polymerized, wherein the shortstopping agent comprises at least two primary alkylhydroxylamines selected from the group consisting of N-ethylhydroxylamine (EHA), N-tertiary-butylhydroxylamine (TBHA), and salts thereof, wherein the EHA and TBHA are present in a weight ratio of from 10:90 to 65:35.

Assignments (7)
CHANGE OF NAME Recorded Sep 21, 2023
From: ANGUS CHEMICAL COMPANY
To: ADVANCION CORPORATION
Reel/Frame 065020/0865 →
PATENT SECURITY AGREEMENT (1ST LIEN) Recorded Dec 1, 2020
From: ANGUS CHEMICAL COMPANY
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 054553/0706 →
PATENT SECURITY AGREEMENT (2ND LIEN) Recorded Dec 1, 2020
From: ANGUS CHEMICAL COMPANY
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 054553/0719 →
RELEASE OF SECURITY INTEREST Recorded Nov 24, 2020
From: JPMORGAN CHASE BANK, N.A.
To: ANGUS CHEMICAL COMPANY
Reel/Frame 054462/0821 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2020
From: COBURN, CHARLES E.; DHAMDHERE, MRUNALINI S.; GUPTE, KAUSTUBH; SAWANT, MAHESH
To: ANGUS CHEMICAL COMPANY
Reel/Frame 053943/0936 →
SUPPLEMENTAL SECURITY AGREEMENT Recorded Jun 10, 2016
From: ANGUS CHEMICAL COMPANY
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 038950/0373 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2016
From: DOW GLOBAL TECHNOLOGIES LLC
To: ANGUS CHEMICAL COMPANY
Reel/Frame 037512/0802 →
Continuity (1)
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