Claims
- 1. A process for preparing a polyarylene sulfide of increased molecular weight comprising admixing a dihalogenated aromatic compound and an undehydrated source of sulfur containing up to 9 moles of water per mole of said source of sulfur in an organic polar solvent without dehydration, and then polycondensing said dihalogenated aromatic compound and said source of sulfur while substantially simultaneously dehydrating the reaction mixture in a single reaction zone under the pressure and temperature at which said polycondensation is performed wherein said pressure and temperature are escalated during said polycondensation and dehydration in a stepwise manner.
- 2. A process as claimed in claim 1, wherein the source of sulfur is an alkali metal sulfide, an alkali metal hydrosulfide or hydrogen sulfide.
- 3. A process as claimed in claim 1, wherein the source of sulfur is a hydrous alkali metal sulfide.
- 4. A process as claimed in claim 1, wherein the dihalogenated aromatic compound is a dihalobenzene.
- 5. A process as claimed in claim 1, wherein the dihalogenated aromatic compound is p-dichlorobenzene.
- 6. A process as claimed in claim 1, wherein the organic polar solvent is a non-protonic organic solvent.
- 7. A process as claimed in claim 1, wherein the organic polar solvent is a lactam.
- 8. A process as claimed in claim 1, wherein the organic polar solvent is a pyrrolidone.
- 9. A process as claimed in claim 1, wherein the pressure ranges from 2 to 10 kg/cm.sup.2.
- 10. A process as claimed in claim 1, wherein polycondensation is carried out at temperature ranging from 220.degree. C. to 300.degree. C.
- 11. In a process for preparing a polyarylene sulfide of increased molecular weight by polycondensing a dihalogenated aromatic compound with a source of sulfur which process comprises first dehydrating said source of sulfur and then polycondensing such dehydrated source of sulfur with said aromatic in an organic polar solvent, the improvement comprising:
- admixing said dihalogenated aromatic compound, an undehydrated source of sulfur, and said organic solvent;
- polycondensing said dihalogenated aromatic compound with said undehydrated source of sulfur in said organic polar solvent while substantially simultaneously dehydrating the reaction mixture under a stepwise escalating pressure up to 2 to 10 kg/cm.sup.2 and at a stepwise escalating temperature up to 220.degree. C. to 300.degree. C.; and
- recovering said polycondensate from said reaction zone.
- 12. The process as claimed in claim 1 wherein said source of sulfur contains up to about 1.2 moles of water per mole, water is added to the reaction mixture, and said polycondensation and said dehydration are carried out batchwise in a single reaction zone.
- 13. The process as claimed in claim 1 wherein said source of sulfur contains at least about 1.2 moles of water per mole of sulfur containing compound.
- 14. A process for preparing a polyarylene sulfide of increased molecular weight consisting essentially of polycondensing a batch of dihalogenated aromatic compound with a source of sulfur containing water in an organic polar solvent in a single reactor while dehydrating the reaction mixture under the pressure at which the polycondensation is carried out wherein said polycondensation and dehydration are carried out under stepwise increasing pressure conditions.
- 15. A process for preparing a polyarylene sulfide having increased molecular weight comprising polycondensing a reaction mixture of a dihalogenated aromatic compound and a source of sulfur containing water in an organic polar solvent, while substantially simultaneously dehydrating the reaction mixture under conditions including pressure and temperature, at which said polycondensation and dehydration is performed wherein said pressure and said temperature are increased during the course of said reaction.
Priority Claims (1)
Number |
Date |
Country |
Kind |
1-168779 |
Jun 1989 |
JPX |
|
Parent Case Info
This application is a continuation of application Ser. No. 546,226, filed Jun. 29, 1990, now abandoned.
US Referenced Citations (11)
Foreign Referenced Citations (4)
Number |
Date |
Country |
59-98133 |
Jun 1984 |
JPX |
59-105027 |
Jun 1984 |
JPX |
60-212429 |
Oct 1985 |
JPX |
2-45531 |
Feb 1990 |
JPX |
Continuations (1)
|
Number |
Date |
Country |
Parent |
546226 |
Jun 1990 |
|