← Back to Patent Explorer
US4182851A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for reducing the residual monomer content in the polymerization of vinyl-lactams and vinyl esters

Assignee: BASF SE
•
Filing: 1978-06-27
•
Granted: 1980-01-08
•
Expires: 1998-06-27
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A process for reducing the residual monomer content of a copolymer prepared by copolymerizing vinyl esters and N-vinyl-lactams in a solvent in the presence of a free radical polymerization initiator. Following the main polymerization, from 0.05 to 0.5% by weight, based on the monomers employed, of di-tert.-butyl peroxide, di-tert.-amyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-bis-(tert.-butylperoxy)-hexane, 2,2-bis-(tert.-butylperoxy)-butane, 1,1-bis-(tert.-butylperoxy)-3,3,5-trimethylcyclohexane, 4,4-di-(tert.-butylperoxy)-butyl valerate, or a mixture of these, is added to the reaction mixture and the after-polymerization is carried out at a higher temperature than the main polymerization.

Inventors

  • 👤 Ferdinand Straub
  • 👤 Herbert Spoor
  • 👤 Hans-Uwe Schenck
  • 👤 Wolfgang Schwarz

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 01:54
CPC Classifications
C; C08; C08F; C08F263/00; C08F263/02; C08F271/00

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 141 words
A process for reducing the residual monomer content in a polymer solution obtained from the copolymerization of vinyl ester and N-vinyl-lactams in a solvent, the copolymer produced containing from 10 to 90% by weight of N-vinyl-lactam and from 90 to 10% by weight of vinyl ester, based on the monomers, which comprises: (a) polymerizing the vinyl esters and N-vinyl-lactams to completion of the polymerization reaction at temperatures of from 45° to 100° C.; (b) adding from 0.05 to 0.5% by weight, based on the monomers employed, of at least one peroxide selected from the group consisting of di-tert.-butyl peroxide, di-tert.-amyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-bis-(tert.-butylperoxy)-hexane, 2,2-bis-(tert.-butyl peroxy)-butane, 1,1-bis-(tert.-butylperoxy)-3,3,5-trimethylcyclohexane or 4,4-di-(tert.-butylperoxy)-butyl valerate, and then (c) after-polymerizing the mixture obtained from step (b) at temperatures of from 110° to 160° C. to reduce the residual monomer content to a value less than about 0.1%.
Claim 2
Dependent Claim 141 words
A process for reducing the residual monomer content in a polymer solution obtained from the copolymerization of vinyl ester and N-vinyl-lactams in a solvent, the copolymer produced containing from 10 to 90% by weight of N-vinyl-lactam and from 90 to 10% by weight of vinyl ester, based on the monomers, which comprises: (a) polymerizing the vinyl esters and N-vinyl-lactams to completion of the polymerization reaction at temperatures of from 45° to 100° C.; (b) adding from 0.05 to 0.5% by weight, based on the monomers employed, of at least one peroxide selected from the group consisting of di-tert.-butyl peroxide, di-tert.-amyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-bis-(tert.-butylperoxy)-hexane, 2,2-bis-(tert.-butyl peroxy)-butane, 1,1-bis-(tert.-butylperoxy)-3,3,5-trimethylcyclohexane or 4,4-di-(tert.-butylperoxy)-butyl valerate, and then (c) after-polymerizing the mixture obtained from step (b) at temperatures of from 110° to 160° C. to reduce the residual monomer content to a value less than about 0.1%.
Claim 3
Dependent Claim 35 words
A process as set forth in claim 1, wherein the polymerization of step (a) is carried out under atmospheric pressure and the after-polymerization is carried out under a pressure of from 1 to 50 bars.
Claim 4
Dependent Claim 15 words
A process as set forth in claim 1, wherein N-vinylpyrrolidone is employed as the vinyl-lactam.
Claim 5
Dependent Claim 20 words
A process as set forth in claim 1, wherein the after-polymerization is carried out for from 0.5 to 5 hours.
Claim 6
Dependent Claim 16 words
A process as set forth in claim 3, wherein the vinyl ester employed is vinyl acetate.

References Cited (Backward Citations)

US2497705A Cited
US2665271A Cited
US2667473A Cited
US2914516A Cited
US4020267A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-01-07 1983-07-09 1984-01-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-01-07 1987-07-09 1988-01-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-01-07 1991-07-09 1992-01-08 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag