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  • Articles: DFG German National Licenses  (8)
  • tensile properties  (6)
  • aromatic polyimides  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1111-1117 
    ISSN: 0887-624X
    Keywords: poly(ether sulfone)-aramid block copolymers ; high-temperature polymers ; solubility ; thermal behavior ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New poly(ether sulfone)-aramid block copolymers were synthesized from an α, ω-diamineterminated poly(ether sulfone) oligomer, aromatic diamines, and aromatic dicarboxylic acid chlorides by the low-temperature solution polycondensation in N-methyl-2-pyrrolidone. By the introduction of aramid into the poly(ether sulfone), the glass transition temperatures of the block copolymers rose and the mechanical properties were significantly improved. Microphase separation, which often takes place in many block copolymers, did not occur in the present block copolymers. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 933-938 
    ISSN: 0887-624X
    Keywords: poly(ether sulfone)-polyimide block copolymers ; high-temperature polymers ; microphase separation ; thermal behavior ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New poly(ether sulfone)-polyimide block copolymers were synthesized from α,ω-diamineterminated poly(ether sulfone) oligomer, aromatic diamines, and aromatic tetracarboxylic dianhydrides by low-temperature solution polymerization and subsequent thermal imidization. The block copolymers were insoluble in organic solvents. The multiblock copolymers obtained by the two-pot method showed microphase separation, while the random block copolymers by the one-pot method had single phase morphology. The mechanical properties of the block copolymers were greatly improved by the introduction of polyimide into the poly(ether sulfone). © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3425-3432 
    ISSN: 0887-624X
    Keywords: polydimethylsiloxane-polyimide block copolymers ; disiloxane-containing random copolyimides ; solubility behavior ; thermal behavior ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New polydimethylsiloxane (PDMS)-polyimide block copolymers were synthesized by the solution polycondensation of aminopropyl-terminated polydimethylsiloxane, 1,1-bis(4-aminophenyl)-2,2-diphenylethylene, and 3,3′,4,4′-benzophenonetetracarboxylic dithioanhydride in pyridine. New 1,3-bis(3-aminopropyl)tetramethyldisiloxane (BADS)-based random copolyimides were also prepared. The inherent viscosities of all the random and block copolyimides were in the range of 0.13-0.90 dL/g in N-methyl-2-pyrrolidone. These copolymers were soluble in N,N-dimethylacetamide, N-methyl-2-pyrrolidone, and m-cresol. All the BADS-based random copolymers and PDMS-containing copolymers with PDMS content above 42 wt % were soluble in tetrahydrofuran and chloroform. Transparent or somewhat cpaque films were prepared by casting from the reaction solutions. The BADS-based random copolyimides had one glass transition temperature (Tg) in the whole composition ranges, which showed single phase nature of the copolymers. On the other hand, the PDMS-polyimide block copolymers had double TgS, indicating phase-separated morphology. The block copolymers containing PDMS content above 73 wt % behaved like a high temperature elastomer. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2021-2027 
    ISSN: 0887-624X
    Keywords: 2,2′-bis(3,4-dicarboxyphenoxy)biphenyl dianhydride ; aromatic polyimides ; solubility ; thermal behavior ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new aromatic tetracarboxylic dianhydride having a crank and twisted noncoplannar structure, 2,2′-bis(3,4-dicarboxyphenoxy)biphenyl dianhydride, was synthesized by the reaction of 4-nitrophthalonitrile with biphenyl-2,2′-diol, followed by hydrolysis and cyclodehydration. The biphenyl-2,2′-diyl-containing aromatic polyimides having inherent viscosities up to 0.66 dL/g were obtained by the conventional two-step procedure starting from the dianhydride monomer and various aromatic diamines. Most of the polyimides were readily soluble in amide-type solvents such as N,N-dimethylacetamide and N-methyl-2-pyrrolidone. The aromatic polyimides had glass transition temperatures in the range of 205-242°C, and began to lose weight around 415°C, with 10% weight loss being recorded at about 500°C in air. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2021-2027, 1998
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0887-624X
    Keywords: disiloxane-containing diamine ; disiloxane-containing copolyamides ; random and block copolyamides ; solubility behavior ; thermal behavior ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Random and block disiloxane-containing copolyamides were prepared through one- and two-step procedures, respectively, by the low temperature solution polycondensation in chloroform containing triethylamine hydrochloride starting from 1,3-bis(3-aminopropyl)tetramethyldisiloxane, an aromatic diamine [3,4'-diaminodiphenyl ether (ODA) or m-phenylenediamine], and isophthaloyl chloride. The random copolyamides exhibited composition-dependent single glass transition temperature (Tg), and gave transparent and tough films by solution casting or hot pressing. The ODA-based block copolyamides had two Tg's, and the solvent-cast transparent films exhibited microphase separated morphology. The block copolymers gave better quality films than the single-phase random copolymers. © 1992 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0887-624X
    Keywords: 2,2′-bis(p-aminophenoxy) biphenyl ; 2,2′-bis(p-aminophenoxy)-1,1′-binaphthyl ; aromatic polyimides ; solubility ; thermal behavior ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New aromatic polyimides containing a biphenyl-2,2′-diyl or 1,1′-binaphthyl-2,2′-diyl unit were prepared by a conventional two-step method starting from 2,2′-bis(p-aminophenoxy) biphenyl or 2,2′-bis(p-aminophenoxy)-1,1′-binaphthyl and aromatic tetracarboxylic dianhydrides. The polyimides having inherent viscosities of 0.69-0.99 and 0.51-0.59 dL/g, respectively, were obtained. Some of these polymers were readily soluble in a variety of organic solvents including N,N-dimethylacetamide (DMAc), N-methyl-2-pyrrolidone (NMP), dimethyl sulfoxide, and pyridine. Transparent, flexible, and pale yellow to brown films of these polymers could be cast from the DMAc or NMP polyamic acid solutions. These aromatic polyimides containing biphenyl and binaphthyl units had glass transition temperatures in the range of 200-235 and 286-358°C, respectively. They began to lose weight around 380°C, with 10% weight loss being recorded at about 470°C in air. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0887-624X
    Keywords: high temperature polymers ; fluorine-containing polyimides ; soluble polyimides ; thermal behavior ; tensile properties ; low dielectric constant polyimides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0887-624X
    Keywords: fluorine-containing polyamides ; copolyamides ; hexafluoroisopropylidene ; isopropylidene ; soluble polyamides ; thermal stability ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic soluble polyamides and copolyamides having hexafluoroisopropylidene and isopropylidene moieties in the molecular structure of polymer chain were prepared by reacting the aromatic diacid chlorides and fluorine or nonfluorine containing aromatic diamines using low-temperature polycondensation process. Polymers were produced with high yield and moderate to high inherent viscosity. All polyimides and copolyamides showed thermal stability above 440°C and glass transition temperature above 200°C. Some of the polyamides were cast into transparent bulk films which were further characterized by mechanical, x-ray, and water absorption analysis. Fluoro polyamides showed superior structural properties as compared to nonfluoro polyamides. © 1996 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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