Method for producing polyarylene sulfide, and polyarylene sulfide
A reactive functional group-containing polyarylene sulfide being narrow in dispersity and little in gas generation amount is produced by heating a cyclic polyarylene sulfide composition in the presence of 0.1 mol % to 25 mol %, per mol of arylene sulfide structural units, of a sulfide compound having a reactive functional group selected from among an amino group, a carboxyl group, a hydroxyl group, an acid anhydride group, an isocyanate group, an epoxy group, a silanol group, and an alkoxysilane group.
1. A method of producing a polyarylene sulfide (c) comprising heating a cyclic polyarylene sulfide composition (a) in the presence of 0.1 mol % to 25 mol %, per mol of arylene sulfide structural units, of a sulfide compound (b) having a reactive functional group represented by formula (A):
wherein at least one of Y and X is a functional group selected from the group consisting of an amino group, a carboxyl group, a hydroxyl group, an acid anhydride group, an isocyanate group, an epoxy group, a silanol group, and an alkoxysilane group, and n represents an integer of 0 to 20.
2. The method according to claim 1 , wherein the cyclic polyarylene sulfide composition (a) comprises 50% by weight or more of a cyclic polyarylene sulfide represented by formula (B), and repetition number m in the formula is 4 to 50;
wherein Ar represents an arylene group.
3. The method according to claim 1 , wherein the heating is performed under a condition containing no solvent.
4. The method according to claim 1 , wherein at least part of the heating is performed under a reduced pressure condition.
5. The method according to claim 1 , wherein the heating temperature is equal to or higher than the melting temperature of a reaction mixture composed of the cyclic polyarylene sulfide composition (a) and the sulfide compound (b) having a reactive functional group.
6. The method according to claim 1 , wherein an amount of the reactive functional groups introduced per mol of the arylene sulfide structural units of the resulting polyarylene sulfide (c) is 0.01 to 5 mol %.
7. The method according to claim 1 , wherein a dispersity represented by weight average molecular weight/number average molecular weight of the resulting polyarylene sulfide (c) is 2.5 or less.
8. The method according to claim 1 , wherein alkali metal content of the resulting polyarylene sulfide (c) is 500 ppm or less.
9. The method according to claim 1 , wherein the resulting polyarylene sulfide (c) has a weight loss ratio at 100 to 330° C. of 0.2% by weight or less when thermogravimetric analysis is performed from 50° C. to 340° C. at a temperature ramp-up rate of 20° C./min under a non-oxidative atmosphere of normal pressure.
10. The method according to claim 1 , wherein the reactive functional group contained in the sulfide compound (b) having a reactive functional group is a group selected the group consisting of an amino group, a carboxyl group, and a hydroxyl group.
11. The method according to claim 1 , wherein the sulfide compound (b) having a reactive functional group is one or more members selected from the group consisting of bis(4-aminophenyl) sulfide, bis(4-carboxyphenyl) sulfide, bis(4-hydroxyphenyl) sulfide, and oligomers thereof.
12. A method of producing a polyarylene sulfide composition (c′) further comprising adding a reactive compound (d) to a polyarylene sulfide (c) obtained by the method according to claim 1 .
13. The method according to claim 12 , wherein the reactive compound (d) is a silane coupling agent having a group selected from the group consisting of an epoxy group, an amino group, and an isocyanate group and an added amount thereof is 0.01 to 5 parts by weight per 100 parts by weight of the polyarylene sulfide (c).
14. The method according to claim 12 , wherein a thickening ratio of the polyarylene sulfide composition (c′) after adding the reactive compound (d) to the polyarylene sulfide (c) before adding the reactive compound (d) is 1.01 or more.