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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 3237-3244 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Fibers were spun from six different, wholly aromatic copolyamides of limited order. Tensile properties of the fibers were obtained at standard conditions and, for selected fibers, at elevated temperatures and after heat-aging at 300°C in air. The dry-heat shrinkage determined up to 400°C on selected fibers was relatively low; zero-strength temperatures ranged from 375°C to 495°C. Resistance to numerous chemical reagents was determined for one of the fibers and found to be comparable to that of the fibers from other wholly aromatic polyamides. Resistance to ultraviolet light appeared to be of the same order as that of unstabilized nylon 66.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1327-1333 
    ISSN: 0887-624X
    Keywords: aromatic polyamides ; polyisophthalamides ; phenylthio pendent groups ; 5-phenylthioisophthalic acid ; phosphorylation polycondensation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyisophthalamides containing pendent phenylthio groups was prepared from seven aromatic diamines and 5-phenylthioisophthalic acid by the phosphorylation polycondensation method. The properties of these polymers were compared with those of the analogous unmodified ones. The modified polymers exhibited better solubility in organic solvents than their unmodified counterparts. They also showed glass transition temperatures that were lower by approximately 30°C. However, the presence of the side groups did not bring about any substantial lowering of the thermal stability as measured by TGA. Other properties investigated were mechanical strength and water sorption.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 873-877 
    ISSN: 0887-624X
    Keywords: 4,4′-diamino-3′-nitrobenzanilide (DNB) ; poly-p-benzamide (PBA) ; poly-p-benzamide end-capped with nitro-p-phenylenediamine ; polyterephthalamide of 4,4′-diamino-3′-nitrobenzanilide ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 653-667 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three types of wholly aromatic block copolymers were synthesized using the phosphorylation reactions of Yamazaki and Higashi. Each copolymer contained blocks of rigid and flexible units. The first copolymer, PBA/PABH-T, contains blocks of poly(p-benzamide) and the polyterephthalamide of p-aminobenzhydrazide. The second copolymer, PBA/MPD-I, contains blocks of poly(p-benzamide) and poly(p-phenylene isophthalamide), whereas the third, PPD T/MPD-I, contains blocks of poly(p-phenylene terephthalamide) and poly(m-phenylene isophthalamide). Three synthetic routes were used for the preparation of the block copolymers. In the two-step polycondensation (A), monomers of the flexible block are added to the rigid prepolymer. The multistep method (B) differs in that the rigid prepolymer is carboxy-terminated prior to addition of the monomers of the flexible block. Carboxy-terminated prepolymer of the rigid block is reacted with amine-terminated prepolymer of the flexible block in the two-pot condensation (C). The presence of a considerable amount of the flexible homopolymer is indicated by viscosity, extraction, and NMR studies, particularly when methods A and C were used. The flexible homopolymer can be extracted by using a nonsolvent for the rigid blocks. Extraction of the rigid homopolymer (which may also be presumed to be produced) entails a more elaborate procedure. In principle, one can use these methods to obtain pure block copolymer for study of mixtures with the rigid and flexible homopolymers. Phase studies of some of these systems will be reported in a following paper.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1175-1195 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four 2,5-biphenylene based difunctional condensation monomers, such as 2,5-diphenyldicar-boxylic acid or phenylterephthalic acid (PTA), 2,5-bis(carbonylimino-4-benzoic acid)biphenyl (2,5-BCIBABP), 2,5-diaminobiphenyl hydrochloride (2,5-DABP.HCl) and 2,5-bis(iminocarbonyl-4-benzoic acid)biphenyl (2,5-BICBABP), have been synthesized and characterized. These monomers were polymerized in combination with terephthalic acid (TA) and p-phenylenediamine (PPD) via the phosphorylation reaction to prepare a series of phenyl-substituted random copolyamides having all amide groups attached to para-positions of the benzene rings. All the copolyamides have been characterized by solubility, solution viscosity, and by differential scanning calorimetry (DSC). Some of these copolyamides have unusual solubility in organic solvents such as N,N-dimethylacetamide (DMAc) and N-methyl-2-pyrrolidinone (NMP) containing dissolved lithium chloride. A few copolyamides were tested for lyotropic behavior and found to form anisotropic solutions at critical concentrations in organic solvents. A randomly distributed unsymmetrical phenyl substituent on the benzene ring of para-oriented wholly aromatic polyamides dramatically changes the solubility and melting point. The phenyl substituent on a terephthalic acid unit is more efficient in decreasing melting point and increasing solubility in organic solvents of aromatic polyamides than the one on a p-phenylenediamine unit. However, the former also introduces a more flexible link in the extended polyamide chain.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 59-63 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
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  • 7
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The history of rigid chain polymers (i.e., polymers that show mesogenic behavior either in the melt or in solution) is traced from its beginnings to the present. Some correlations between certain mesogenic structures and the physical properties of the corresponding polymers are drawn, particularly as they relate to fibers and to a lesser degree to films and molding resins. Some factors relating to the processing of rod-like polymers from thermotropic melts and from lyotropic solutions are dealt with, and some end use applications for rigid chain polymers are given.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 713-715 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 1804-1805 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 1109-1113 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The trifunctional monomers trimesic acid (TMA) and 3,5-diaminobenzoic acid (DAB), each separately and in combination, were used in amounts of 2 to 5 mole-% in order to increase the molecular weight of aromatic polyamides prepared via the Yamazaki phosphorylation reaction. In general, under comparable conditions the use of DAB led to polymer having higher inherent viscosity (IV) values than did TMA. A typical polymer was the polyisophthalamide of 4,4′-methylenedianiline, MDA-I, prepared by the reaction at 100°C of 4,4′-methylenedianiline (MDA) with isophthalic acid (I) in N-methylpyrrolidione (containing 5% dissolved lithium chloride) and employing triphenyl phosphite as condensation agent with pyridine as catalyst. For molar substitutions of 0.0, 2.0, 2.5, and 3.0% of DAB, MDA-I having IV values respectively of 1.1, 1.3, 1.9, and 2.3 was obtained. The latter two samples have IV values in the same range as those obtained for MDA-I prepared from MDA and isophthaloyl chloride in dimethylacetamide (DMAc) via the low-temperature polycondensation method, which prior experience has shown yields polymers that are quite suitable for the spinning of good fibers. At 5 mole-% substitution of DAB, an IV of 3.7 was obtained but a large quantity of gel particles was observed on dissolving the sample in DMAc containing 5% LiCl, indicating that considerable crosslinking had probably occurred. The rod-like polymer poly-p-benzamide (PPB) was prepared in similar fashion to MDA-I from p-aminobenzoic acid and IV values of respectively 1.6, 2.3, 3.8, and 3.9 were obtained when 0.0, 2.0, 2.5, and 3.0 mole-% of mixed trifunctional monomers were present. A solution of the latter sample dissolved in concentrated sulfuric acid contained considerable gel, indicating that crosslinked polymer was probably produced. It would appear that the chain branching approach for producing high molecular weight PPB for spinning to fibers will not prove useful because PPB having an IV value of about 3 to 4 is considered only marginal for the production of commercial-quality fibers (even though PPB of IV value 1.6 can be spun to high-strength/high-modulus fibers) and because the requisite balance of strength and modulus to elongation to break are only obtained for fibers from PPB having an IV value above about 3.5, and preferably about 5 to 6.
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