Method of preparing polyphenylene sulfide and high-viscosity polyphenylene sulfide prepared using the same

Patent metadata

Field	Value
Publication number	US-10941249-B2
Application number	US-201716320420-A
Country	US
Kind code	B2
Filing date	Nov 14, 2017
Priority date	Dec 23, 2016
Publication date	Mar 9, 2021
Grant date	Mar 9, 2021

Abstract

The present invention relates to a method of preparing a polyphenylene sulfide and a high-viscosity polyphenylene sulfide prepared using the method. In this method, the ratio of an organic phase to an aqueous phase is controlled by controlling dehydration conditions, so that high viscosity may be realized without adversely affecting a reaction or physical properties during preparation of the polyphenylene sulfide.

First claim

The invention claimed is:

1. A method of preparing a polyphenylene sulfide, comprising:
(a) a step of mixing a sulfur source, an alkali metal hydroxide, a polymerization agent, an organic solvent, and water to obtain an initial mixture;
(b) a step of heating the initial mixture while stirring to obtain a residual mixture; and
(c) a step of adding a dihalogenated aromatic compound and an organic solvent to the residual mixture to obtain a mixed solution, and polymerizing the mixed solution,
wherein in step (b), a molar ratio of water to sulfur (H 2 O/S) in the residual mixture is 2.14 to 2.5, and
wherein in step (c), a molar ratio of water to the organic solvent (H 2 O/organic solvent) in the mixed solution is 0.5 to 0.85.

2. The method according to claim 1 , wherein the sulfur source is one or more selected from the group consisting of sodium hydrogen sulfate, sodium sulfide, and potassium sulfide.

3. The method according to claim 1 , wherein the polymerization agent is one or more selected from the group consisting of an organic acid metal salt, an alkali metal chloride, an organic sulfonate, and an alkali metal sulfate.

4. The method according to claim 1 , wherein the organic solvent is one or more selected from the group consisting of an alcohol, an alkylene oxide, N-methylpyrrolidone, and a polyhydric alcohol.

5. The method according to claim 1 , wherein, in step (b), the mixture is heated to a temperature of 130 to 210° C. and stirred to reduce an amount of water.

6. The method according to claim 1 , wherein the dihalogenated aromatic compound is one or more selected from the group consisting of polyhalogenated aromatic compounds consisting of p-dichlorobenzene, m-dichlorobenzene, o-dichlorobenzene, 1,3,5-trichlorobenzene, 1,2,4-trichlorobenzene, 1,2,4,5-tetrachlorobenzene, hexachlorobenzene, 2,5-dichlorotoluene, 2,5-dichloro-p-xylene, 1,4-dibromobenzene, 1,4-diiodobenzene, and 1-methoxy-2,5-dichlorobenzene.

7. The method according to claim 1 , wherein an equivalence ratio (S/DH) of the sulfur source (S) in step (a) to the dihalogenated aromatic compound (DH) in step (c) is 0.80 to 1.30.

8. The method according to claim 1 , wherein an equivalence ratio (WM/S) of the polymerization agent (WM) to the sulfur source (S) in step (a) is 0.05 to 1.0.

9. The method according to claim 1 , wherein, in step (c), the polymerization is performed by heating the mixed solution to a temperature of 200 to 280° C. and stirring the mixed solution.

Assignees

• Lg Chemical Ltd

Inventors

• Jung Kwonsu
• Han Joong Jin
• Park Eun Ju
• Ryu Hyun Woog

Classifications

• C08G75/0259

  metal hydrogensulfides · CPC title

• C08L81/02

  Polythioethers; Polythioether-ethers · CPC title

• C08G75/14 Primary

  Polysulfides · CPC title

• C08G75/02 Primary

  Polythioethers · CPC title

• C08G75/0254

  using metal sulfides · CPC title