Patent US5509108A successfully refreshed from Google Patents.
Patent US4663430A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4663430A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of high molecular weight polyarylene sulphide in the absence of water

Assignee: Bayer AG
•
Filing: 1986-01-02
•
Granted: 1987-05-05
•
Expires: 2006-01-02
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract This invention relates to a process for the preparation of high molecular weight, optionally branched polyarylene sulphides. These may be prepared from alkali metal sulphides and aromatic halogen compounds in a polar organic solvent in the absence of water.

Inventors

  • 👤 Edgar Ostlinning
  • 👤 Karsten Idel

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 14:50
CPC Classifications
C; C08; C08G; C08G75/00; C08G75/02; C08G75/0204; C08G75/025; C08G75/0254; C08G75/0231

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 270 words
Process for the preparation of high molecular weight polyarylene sulphide having a viscosity of from 0.3×10 3 to 5×10 6 Pascal units which comprises reacting in the absence of water (a) 0-100 mol-% of at least one aromatic dihalogen compound corresponding to the formula ##STR3## and 100-0 mol-% of at least one aromatic dihalogen compound corresponding to the formula ##STR4## wherein X represents halogens in the meta- or para-position to each other and R 1 , which is identical or different, represents hydrogen, alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl and two groups R 1 in the ortho-position to each other are linked together to form an aromatic or heterocyclic ring and one group R 1 is invariably different from hydrogen and (b) 0-5 mol-% based on the sum of components (a) and (b), of an aromatic trihalogen or tetrahalogen compound corresponding to the formula ArX.sub.n (III) wherein Ar represents an aromatic or heterocyclic group, X represents chlorine or bromine and n represents 3 or 4, and (c) alkali metal sulphide alone or together with alkali metal hydroxide, the molar ratio of (a+b):c is within the range of 0.85:1 to 1.15:1, and (d) in an organic solvent which is an N-alkyllactam having a boiling point above 200° C., characterized in that the molar ratio of alkali metal sulphide (c) to organic solvent (d) is within the range of 1:2 to 1:15 and the alkali metal sulphide is dehydrated either solvent-free or in a polar organic solvent with or without the aid of an inert H 2 O carrier before addition of the aromatic halogen compounds of formulae I, II or III.
Claim 2
Dependent Claim 270 words
Process for the preparation of high molecular weight polyarylene sulphide having a viscosity of from 0.3×10 3 to 5×10 6 Pascal units which comprises reacting in the absence of water (a) 0-100 mol-% of at least one aromatic dihalogen compound corresponding to the formula ##STR3## and 100-0 mol-% of at least one aromatic dihalogen compound corresponding to the formula ##STR4## wherein X represents halogens in the meta- or para-position to each other and R 1 , which is identical or different, represents hydrogen, alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl and two groups R 1 in the ortho-position to each other are linked together to form an aromatic or heterocyclic ring and one group R 1 is invariably different from hydrogen and (b) 0-5 mol-% based on the sum of components (a) and (b), of an aromatic trihalogen or tetrahalogen compound corresponding to the formula ArX.sub.n (III) wherein Ar represents an aromatic or heterocyclic group, X represents chlorine or bromine and n represents 3 or 4, and (c) alkali metal sulphide alone or together with alkali metal hydroxide, the molar ratio of (a+b):c is within the range of 0.85:1 to 1.15:1, and (d) in an organic solvent which is an N-alkyllactam having a boiling point above 200° C., characterized in that the molar ratio of alkali metal sulphide (c) to organic solvent (d) is within the range of 1:2 to 1:15 and the alkali metal sulphide is dehydrated either solvent-free or in a polar organic solvent with or without the aid of an inert H 2 O carrier before addition of the aromatic halogen compounds of formulae I, II or III.
Claim 3
Dependent Claim 15 words
Process according to claim 1 wherein the reaction temperature is from 170° to 270° C.
Claim 4
Dependent Claim 14 words
Process according to claim 1 wherein the polar organic solvent is N-methylcaprolactam or N-ethylcaprolactam.
Claim 5
Dependent Claim 14 words
Process according to claim 1 wherein (d) further comprises, N,N-dialkylcarboxylic acid amide as cosolvent.
Claim 6
Dependent Claim 11 words
Process according to claim 1 wherein toluene is the inert carrier.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-05-04 1990-11-03 1991-05-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-05-04 1994-11-03 1995-05-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-05-04 1998-11-03 1999-05-05 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag