US4169932A
Expired / Lapsed
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Method of producing poly-p-phenyleneterephthalamide or its copolymers
Assignee: Ingersoll Equipment Co Inc
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Filing: 1978-08-11
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Granted: 1979-10-02
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Expires: 1998-08-11
Abstract
Abstract A method of producing poly-p-phenyleneterephthalamide or its copolymers residing in that p-phenylenediamine or p-phenylenediamine and an aromatic diamine of the diphenyl series is/are disclosed in amide-salt solvents consisting of linear or cyclic N-alkyl-substituted amides of acids and of salts of alkaline or alkaline-earth metals soluble in said amides in amounts of 1-3 moles per mole of diamines; terephthalic acid dichloride or a mixture of terephthalic acid dichloride and aromatic acid dichloride of the diphenyl series are introduced into the solutions obtained at 0°-20° C. in amounts equimolar to those of the diamines, a reaction mixture being thus formed; tertiary amines are introduced into said reaction mixture in amounts 2-6 moles per mole of the initial diamines; the reaction mixture is stirred for 3-70 minutes and the end product is separated from the mass obtained. The method proposed herein is technologically simple and provides high-molecular polymeric products suitable for manufacturing heat-resistant, high-strength, and high-modulus fibres.
Inventors
- 👤 Lev B. Sokolov
- 👤 Valentin M. Savinov
- 👤 Vyacheslav S. Petrukhin
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-01 23:39
CPC Classifications
C; C08; C08G; C08G69/00; C08G69/38
Claims Analysis
Total Claims: 5
Claim 1
Independent Claim
292 words
A process for producing a fiber forming poly-para-phenyleneterephthalamide or a copoly-para-phenyleneterephthalamide comprising the steps of: (1) dissolving para-phenylenediamine or a mixture of 50 to 95 mol. percent of p-phenylenediamine with 50 to 5 mol. percent of an aromatic diamine of the diphenyl series selected from the group consisting of benzidine, 4,4'-diaminodiphenyl oxide, 4,4'-diaminodiphenyl sulfone, 4,4'-diaminobenzophenone, ortho-tolidine, ortho-dianisidine, in an amide-salt solvent in which the metal salt is used in an amount of between 1 and 3 mole per mole of the dissolved aromatic diamines and is selected from the group consisting of organic or inorganic alkali or alkaline earth metal salts soluble in the amide solvent and in which the amide solvent is selected from the group consisting of linear N-dialkyl-substituted carbamic acids, lower aliphatic acids and inner cyclic N-alkyl-substituted amides of aliphatic aminoacids, to obtain a solution thereof; (2) adding to said solution with stirring at a temperature in the range of from about 0° to +20° C. terephthalic acid dichloride or a mixture of 50 to 95 molar percent of terephthalic acid dichloride with 50 to 5 molar percent of a dichloride of an aromatic diacid of the diphenyl series selected from the group consisting of diphenyl-4,4'-dicarboxylic acid dichloride, diphenyloxide-4,4'-dicarboxylic acid dichloride, benzophenone-4,4'-dicarboxylic acid dichloride in which said aromatic diacid dichloride is employed in equimolar amounts with said aromatic diamine, to obtain a homogeneous reaction mixture; (3) adding to said reaction mixture, with stirring, a tertiary amine selected from the group consisting of α-picoline, β-picoline, N,N-dimethylbenzylamine, N,N-dimethylaniline, quinoline, pyridine, triethylamine, N-methylmorpholine, in an amount of from 2 to 6 moles per mole of the starting aromatic diamines; (4) stirring the resulting reaction mixture for a period of from 3 to 70 minutes to obtain poly-para-phenyleneterephthalamide, and (5) separating the resulting
Claim 2
Dependent Claim
292 words
A process for producing a fiber forming poly-para-phenyleneterephthalamide or a copoly-para-phenyleneterephthalamide comprising the steps of: (1) dissolving para-phenylenediamine or a mixture of 50 to 95 mol. percent of p-phenylenediamine with 50 to 5 mol. percent of an aromatic diamine of the diphenyl series selected from the group consisting of benzidine, 4,4'-diaminodiphenyl oxide, 4,4'-diaminodiphenyl sulfone, 4,4'-diaminobenzophenone, ortho-tolidine, ortho-dianisidine, in an amide-salt solvent in which the metal salt is used in an amount of between 1 and 3 mole per mole of the dissolved aromatic diamines and is selected from the group consisting of organic or inorganic alkali or alkaline earth metal salts soluble in the amide solvent and in which the amide solvent is selected from the group consisting of linear N-dialkyl-substituted carbamic acids, lower aliphatic acids and inner cyclic N-alkyl-substituted amides of aliphatic aminoacids, to obtain a solution thereof; (2) adding to said solution with stirring at a temperature in the range of from about 0° to +20° C. terephthalic acid dichloride or a mixture of 50 to 95 molar percent of terephthalic acid dichloride with 50 to 5 molar percent of a dichloride of an aromatic diacid of the diphenyl series selected from the group consisting of diphenyl-4,4'-dicarboxylic acid dichloride, diphenyloxide-4,4'-dicarboxylic acid dichloride, benzophenone-4,4'-dicarboxylic acid dichloride in which said aromatic diacid dichloride is employed in equimolar amounts with said aromatic diamine, to obtain a homogeneous reaction mixture; (3) adding to said reaction mixture, with stirring, a tertiary amine selected from the group consisting of α-picoline, β-picoline, N,N-dimethylbenzylamine, N,N-dimethylaniline, quinoline, pyridine, triethylamine, N-methylmorpholine, in an amount of from 2 to 6 moles per mole of the starting aromatic diamines; (4) stirring the resulting reaction mixture for a period of from 3 to 70 minutes to obtain poly-para-phenyleneterephthalamide, and (5) separating the resulting
Claim 3
Dependent Claim
38 words
A process as claimed in claim 1, wherein in preparing aromatic diamine solutions, the para-phenylene-diamine is used in the form of para-phenylene-diamine dihydrochloride and wherein 2 to 4 moles of tertiary amine per mole of para-phenylenediamine dihydrochloride is
Claim 4
Dependent Claim
41 words
A process as claimed in claim 1, wherein said amide-salt solvent is selected from the group consisting of dimethylacetamide and lithium chloride, dimethylacetamide and calcium chloride, diethylacetamide and lithium chloride, N-methylpyrrolidone and lithium chloride, dimethylacetamide and magnesium chloride, dimethylacetamide and lithium
Claim 5
Dependent Claim
36 words
A process as claimed in claim 1, wherein, in order to prepare the desired poly-para-phenyleneterephthalamide in the form of granules, the product of the process of claim 1 is granulated, the granules are washed and dried.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-10-01 | 1983-04-02 | 1983-10-02 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-10-01 | 1987-04-02 | 1987-10-02 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-10-01 | 1991-04-02 | 1991-10-02 | $7700.00 | Window Closed / Lapsed |