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Process for the preparation of polyarylene sulphides

Assignee: Bayer AG
•
Filing: 1982-09-13
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Granted: 1984-01-03
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Expires: 2002-09-13
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Abstract

Abstract Process for preparing polyarylensulfides by reacting dihalogenobenzenes, optionally substituted with polyhalogenoaromatic compounds with 3 or 4 halogeno substituents, and alkali metal sulfide in polar solvents using alkali metal sulfites and/or alkaline earth metal sulfites as catalysts.

Inventors

  • 👤 Karsten Idel
  • 👤 Edgar Ostlinning
  • 👤 Dieter Freitag
  • 👤 Ludwig Bottenbruch

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 22:44
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 253 words
Process for the preparation of high molecular weight branched polyarylene sulphides, characterised in that (a) dihalogenobenzenes, of which 50 to 100 mole % correspond to the formula I ##STR3## and 0 to 50 mole % correspond to the formula II ##STR4## wherein X is fluorine, chlorine, bromine or iodine, and R 1 is identical or different and is hydrogen, C 1 -C 20 -alkyl, C 5 -C 20 -cycloalkyl, C 6 -C 24 -aryl, C 7 -C 24 -alkaryl or C 7 -C 24 -aralkyl, or at least one pair of radicals R 1 can be linked to an aromatic or heterocyclic ring, and always at least one radical R 1 is different from hydrogen, and (b) 0.1 to 2.4 mole %, relative to the dihalogenobenzenes, of a polyhalogenoaromatic of the formula III, ArX.sub.n (III) wherein Ar is a trivalent or tetravalent aromatic or heterocyclic radical having 6-24 C atoms, X has the same meaning as in formula I and II, and n=3 or 4, and (c) an alkali metal sulphide are reacted in (d) a polar solvent, the molar ratio of (a) to (c) being in the range from 0.85:1 to 1.15:1, and (c) to (d) in the range from 1:2 to 1:15, a polycondensation time of up to 10 hours and a polycondensation temperature from 160° to 300° C. being maintained, and the reaction being carried out in the presence of 2 to 30 mole %, relative to alkali metal sulphide, of an alkali metal sulphite and/or alkaline earth metal sulphite.
Claim 2
Dependent Claim 253 words
Process for the preparation of high molecular weight branched polyarylene sulphides, characterised in that (a) dihalogenobenzenes, of which 50 to 100 mole % correspond to the formula I ##STR3## and 0 to 50 mole % correspond to the formula II ##STR4## wherein X is fluorine, chlorine, bromine or iodine, and R 1 is identical or different and is hydrogen, C 1 -C 20 -alkyl, C 5 -C 20 -cycloalkyl, C 6 -C 24 -aryl, C 7 -C 24 -alkaryl or C 7 -C 24 -aralkyl, or at least one pair of radicals R 1 can be linked to an aromatic or heterocyclic ring, and always at least one radical R 1 is different from hydrogen, and (b) 0.1 to 2.4 mole %, relative to the dihalogenobenzenes, of a polyhalogenoaromatic of the formula III, ArX.sub.n (III) wherein Ar is a trivalent or tetravalent aromatic or heterocyclic radical having 6-24 C atoms, X has the same meaning as in formula I and II, and n=3 or 4, and (c) an alkali metal sulphide are reacted in (d) a polar solvent, the molar ratio of (a) to (c) being in the range from 0.85:1 to 1.15:1, and (c) to (d) in the range from 1:2 to 1:15, a polycondensation time of up to 10 hours and a polycondensation temperature from 160° to 300° C. being maintained, and the reaction being carried out in the presence of 2 to 30 mole %, relative to alkali metal sulphide, of an alkali metal sulphite and/or alkaline earth metal sulphite.
Claim 3
Dependent Claim 16 words
Process according to claim 1, characterised in that p-dichlorobenzene or p-dibromobenzene is employed as component (a).
Claim 4
Dependent Claim 25 words
Process according to claim 1, characterised in that 0.4 to 2.0 mole %, relative to dihalogenobenzene, of a polyhalogenoaromatic of the formula III is employed.
Claim 5
Dependent Claim 26 words
Process according to claim 1, characterised in that 2 to 30 mole %, relative to alkali metal sulphide, of sodium sulphite or potassium sulphite are employed.
Claim 6
Dependent Claim 21 words
Process according to claim 1, characterised in that at least one amide completely alkylated at the nitrogen is employed as solvent.

References Cited (Backward Citations)

US3354129A Cited
US3763124A Cited
US3919177A Cited
US4116947A Cited
DE2817731A1 Cited
US4331801A Cited
US4362864A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-01-02 1987-07-04 1988-01-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-01-02 1991-07-04 1992-01-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-01-02 1995-07-04 1996-01-03 $7700.00 Window Closed / Lapsed

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