GB898651A - Polymers containing polyamide-acid recurring units and their production - Google Patents

Polymers containing polyamide-acid recurring units and their production

Info

Publication number
GB898651A
GB898651A GB3181159A GB3181159A GB898651A GB 898651 A GB898651 A GB 898651A GB 3181159 A GB3181159 A GB 3181159A GB 3181159 A GB3181159 A GB 3181159A GB 898651 A GB898651 A GB 898651A
Authority
GB
United Kingdom
Prior art keywords
diamine
bis
dimethyl
tetracarboxylic
phenylene diamine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3181159A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB898651A publication Critical patent/GB898651A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • C08G73/1007Preparatory processes from tetracarboxylic acids or derivatives and diamines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Polyamides (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

Polyamide-acids having the recurring unit:- <FORM:0898651/IV (a)/1> or <FORM:0898651/IV (a)/2> where R is a tetravalent radical containing at least 2 carbon atoms, no more than 2 carbonyl groups of each polyamide-acid unit being attached to any one carbon atom of said tetravalent radical, R1 is a divalent radical containing at least 2 carbon atoms, the amide groups of adjacent polyamide-acid units each attached to separate carbon atoms of said divalent radical, said polyamide-acid having an inherent viscosity measured at 30 DEG C. at a concentration of 0,5% by weight of the polymer are made by reacting at least one diamine of the formula H2N-R1-NH2 with at least one tetracarboxylic acid dianhydride having the structural formula <FORM:0898651/IV (a)/3> in an organic solvent for the product and at least one of the reactants whose functional groups do not react with either of the reactants to a greater extent than the reactants do with each other, under substantially anhydrous conditions at a temperature below 60 DEG C. The polyamide-acid may be separated from the reaction mixture by precipitating in a non-solvent such as cyclohexane, dioxane or benzene. Many diamines are specified, examples being m-phenylene diamine, p-phenylene diamine, benzidine, hexamethylene diamine, 3-methoxyhexamethylene diamine, 2:11-diaminododecane and piperazine. Specified tetracarboxylic acid dianhydrides are pyromellitic, 2,3,6,7-naphthalene tetracarboxylic, 3,31,4,41-diphenyl tetracarboxylic, 1,2,5,6-naphthalene tetracarboxylic, 2,21,3,31-diphenyl tetracarboxylic, 2,2-bis(3,4-dicarboxyphenyl)propane, 3,4-dicarboxyphenyl sulphone, perylene 3,4,9,10-tetracarboxylic, bis(3,4-dicarboxyphenyl) ether and ethylene tetracarboxylic dianhydride. Specified solvents are N,N-dimethyl formamide, N, N-dimethyl acetamide, N,N-diethyl formamide, N,N-diethylacetamide, N,N-dimethyl methoxy acetamide, N-methyl caprolactam, dimethyl sulphoxide, N-methyl-2-pyrrolidone, tetramethylene urea, pyridine, dimethyl sulphone, hexamethyl phosphoramide, tetramethylene sulphone, formamide, N-methyl formamide and N-acetyl-2-pyrrolidone alone or in combination with benzene, benzonitrile, dioxane, butyrolactone, xylene, toluene and cyclohexane. In the Examples:- (1), (7), (11) to (13), (22) and (23) m-phenylene diamine; (2) p-phenylene diamine; (3) and (14) benzidine; (4) m-phenylene diamine, p-phenylene diamine and benzidine; (5) 2,2-bis(4-aminophenyl)propane; (6) m-phenylene diamine and bis(4-aminophenyl)methane; (8) bis(4-aminophenyl) methane; (9) m-phenylene diamine and hexamethylene diamine; (10) 4,41-diaminodiphenyl methane and hexamethylene diamine; (15) m-xylylene diamine; (16) 2:11-dodecane diamine; (17) hexamethylene diamine; (18) 4,4-dimethylheptamethylene diamine; (19) and (20) bis(p-aminophenyl) ether; (21) 4,41-diaminodiphenyl methane; (24) diaminodiphenyl sulphide; (25) bis(4-aminophenyl) sulphone and 26) 4,41-diaminodiphenyl ether are reacted with:- (1) to (11), (15) to (19) and (21) to (26) pyromellitic dianhydride; (12) pyromellitic dianhydride and phthalic anhydride; (13), (14) and (25) 2,2-bis(dicarboxyphenyl) propane in the presence of:- (1), (2), (12) to (16), (19) and (26) N:N-dimethyl acetamide; (3) to (11), (17), (18), (21), (22) and (25) N:N-dimethyl formamide (20) pyridine; (23) dimethyl sulphoxide and (24) pyridine and dimethyl formamide.
GB3181159A 1958-09-19 1959-09-18 Polymers containing polyamide-acid recurring units and their production Expired GB898651A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US76196858A 1958-09-19 1958-09-19

Publications (1)

Publication Number Publication Date
GB898651A true GB898651A (en) 1962-06-14

Family

ID=25063747

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3181159A Expired GB898651A (en) 1958-09-19 1959-09-18 Polymers containing polyamide-acid recurring units and their production

Country Status (4)

Country Link
CH (1) CH424259A (en)
DE (2) DE1420706C3 (en)
DK (1) DK107258C (en)
GB (1) GB898651A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3349061A (en) * 1964-01-10 1967-10-24 Du Pont Amide-ester isomers
US4470944A (en) * 1982-02-23 1984-09-11 Toray Industries, Inc. Process for producing an aromatic polyimide film
EP0859023A2 (en) * 1997-02-15 1998-08-19 Dr.Beck & Co. Aktiengesellschaft Mixtures of solutions of polyamidocarboxylic acids and solutions of polyimid precusors
DE102014104223A1 (en) 2014-03-26 2015-10-01 Elantas Italia S.R.L. New solvent for polyamide-imides and polyimides
WO2019038154A1 (en) 2017-08-23 2019-02-28 Heraeus Noblelight Gmbh Method and device for producing a polyimide coating on a substrate

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4269968A (en) * 1979-11-13 1981-05-26 International Business Machines Corporation Synthesis of polyamic acid

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3349061A (en) * 1964-01-10 1967-10-24 Du Pont Amide-ester isomers
US4470944A (en) * 1982-02-23 1984-09-11 Toray Industries, Inc. Process for producing an aromatic polyimide film
EP0859023A2 (en) * 1997-02-15 1998-08-19 Dr.Beck & Co. Aktiengesellschaft Mixtures of solutions of polyamidocarboxylic acids and solutions of polyimid precusors
EP0859023A3 (en) * 1997-02-15 1999-04-21 Dr.Beck & Co. Aktiengesellschaft Mixtures of solutions of polyamidocarboxylic acids and solutions of polyimid precusors
US6074757A (en) * 1997-02-15 2000-06-13 Schenectady Europe Gmbh Mixtures of solutions of polyamidocarboxylic acids and solutions of polyimide-forming starting materials
DE102014104223A1 (en) 2014-03-26 2015-10-01 Elantas Italia S.R.L. New solvent for polyamide-imides and polyimides
WO2015144663A1 (en) 2014-03-26 2015-10-01 Elantas Italia S. R. L. Novel solvent for polyamide imides and polyimides
WO2019038154A1 (en) 2017-08-23 2019-02-28 Heraeus Noblelight Gmbh Method and device for producing a polyimide coating on a substrate

Also Published As

Publication number Publication date
DK107258C (en) 1967-05-08
DE1420706A1 (en) 1968-10-10
DE1795611C3 (en) 1975-11-06
DE1795611A1 (en) 1972-01-27
DE1420706B2 (en) 1971-08-19
DE1795611B2 (en) 1975-03-06
CH424259A (en) 1966-11-15
DE1420706C3 (en) 1974-05-09

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