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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 2103-2108 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 2093-2102 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 449-452 (Mar. 2004), p. 1157-1160 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A series of polybenzoxazine-silica hybrids was papered by blending benzoxazinemonomer with various ratios of tetraethoxysilane (TEOS) as a precursor for silica. The blendsafter hydrolysis and condensation of TEOS were thermally treated gradually up to 240oC to affordthe hybrids. The IR spectra and DSC showed the completion of the ring opening of benzoxazinemonomer and formation of silica by the end of the 240oC cure. The inclusion of silica intopolybenzoxazine matrix has a noticeable effect on the thermal and mechanical properties
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  • 5
    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: Graphite-reinforced composites were prepared with oligomeric polyimides having biphenylene end-caps and acetylene linkages in the polymer chain. The oligomers were crosslinked by the reaction of the biphenylenes with the diphenyl acetylenes to form 9,10-diphenylphenanthrene units. The resulting composites had good mechanical properties. Thermal oxidative aging studies show that the unidirectional graphite fiber composites maintained good mechanical properties up to 1200 h at 316°C.
    Additional Material: 12 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2205-2211 
    ISSN: 0887-624X
    Keywords: internal acetylene ; crosslinking ; polyimide ; para ; thermally curable ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crosslinking behavior of internal acetylene units linked para to the aromatic rings was investigated by preparing polyimide from 4,4′-diaminodiphenylacetylene (p-intA) and 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA). Polyimide was also prepared from 1,4-phenylenediamine (PDA) and 6FDA for comparison. The polymers were moderately to highly viscous at the stage of polyamide acid. Thermal imidization gave polyimide having acetylene units that are linked para to the aromatic connecting units. Differential scanning calorimetry (DSC) measurement of the polymer revealed that exotherm due to the crosslinking of the acetylene unit appeared at ca. 330°C. After thermal treatment at high temperature such as 350 and 400°C, onset of the exotherm shifted to higher temperature and the amount of the exotherm became smaller. The dynamic mechanical properties of the uncrosslinked polyimide film treated at 250°C had a glass transition temperature (Tg) at 330°C with a considerable drop in the storage modulus at this temperature. After the film was exposed to a higher temperature to induce crosslinking, the Tg was observed to increase to above 400°C and the storage modulus was maintained to higher temperatures. Tensile properties of the polyimide showed that the films had good mechanical properties. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3745-3753 
    ISSN: 0887-624X
    Keywords: poly(urethane-imide) ; polyurethane ; polyimide ; poly(amide acid) ; oligo(amide acid) ; polyurethane prepolymer ; elastomer ; polymer network ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polymer blend consisting of polyimide (PI) and polyurethane (PU) was prepared by means of a novel approach. PU prepolymer was prepared by the reaction of polyester polyol and 2,4-tolylenediisocyanate (2,4-TDI) and then end-capped with phenol. Poly(amide acid) was prepared from pyromellitic dianhydride (PMDA) and oxydianiline (ODA). A series of oligo(amide acid)s were also prepared by controlling the molar ratio of PMDA and ODA. The PU prepolymer and poly(amide acid) or oligo(amide acid) solution were blended at room temperature in various weight ratios. The cast films were obtained from the blend solution and treated at various temperatures. With the increase of polyurethane component, the films changed from plastic to brittle and then to elastic. The poly(urethane-imide) elastomers showed excellent mechanical properties and moderate thermal stability. The elongation of films with elasticity was more than 300%. The elongation set after the breaking of films was small. From the dynamic mechanical analysis, all the samples showed a glass transition temperature (Tg) at ca. -15°C, corresponding to Tg of the urethane component, suggesting that phase separation occurred between the two polymer components, irrespective of polyimide content. TGA and DSC studies indicated that the thermal degradation of poly(urethane-imide) was in the temperature range 250-270°C. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3745-3753, 1997
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3377-3385 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A N-Methylpyrrolidone (NMP) solution of polymic acid having internal acetylene units in the backbone was mixed with a NMP solution of oligomeric amic acid end-capped with biphenylenes to afford a miscible solution. The viscosity of polymic acid solution lowered considerably by the addition of oligomers, which could lead to improved processability. The amic acid mixture was thermally or chemically cyclized to give a blend of internal-reactive polymide and end-reactive oligoimide. Films of imide blends were easily prepared by casting solutions of the amic acid blends followed by imidization. The imide blends were thermally cured at 400°C for 10 min to give cross-linked polyimides that showed excellent thermal stability as confirmed by DSC, TGA, TMA, and viscoelastic analyses of the cured films. A selective co-crosslinking reaction between biphenylene in the oligomide and acetylene in the polyimide to give phenanthrene linkage is supposed to be the cause of the high thermal stability.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2395-2402 
    ISSN: 0887-624X
    Keywords: internal acetylene ; crosslinking ; polyimide ; thermally curable ; high modulus ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4,4′-Diaminodiphenylacetylene (p-intA) was reacted with 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA), 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) and pyromellitic dianhydride (PMDA) in N-methyl-2-pyrrolidone (NMP) to give poly(amic acid) solution of moderate to high viscosity. Thermal imidization gave polyimide having acetylene units that are linked para to the aromatic connecting unit. Polyimide having acetylene units that are linked meta to the aromatic connecting unit also was prepared utilizing 3,3′-diaminodiphenylacetylene (m-intA) for comparison. The crosslinking behavior of the acetylene units was observed with DSC. Exotherm due to the crosslinking of the para-linked acetylene units appeared at ca. 340 to 380°C depending on the structure of polyimide, whereas meta-linked acetylene units appeared at lower temperature as 340-350°C. After thermal treatment at high temperature such as 350 or 400°C, the amount of the exotherm became smaller and finally disappeared on DSC, confirming the progress of crosslinking. Dynamic mechanical properties of the polyimide films show that glass transition temperature increased with higher heat treatment, also confirming the progress of crosslinking. Tensile properties of the polyimide films showed that rigid polyimide films consisting of p-intA with BPDA or PMDA have considerably higher modulus than those consisting of m-intA. Cold-drawing of the poly(amic acid) followed by imidization gave much higher modulus in the case of rigid polyimide. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2395-2402, 1997
    Additional Material: 15 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1989-1994 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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