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  • 1975-1979  (12)
  • 1979  (10)
  • 1977  (2)
Material
Years
  • 1975-1979  (12)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 3541-3552 
    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: Polyimide fibers were prepared by wet spinning of poly(p,p′ -diaminodiphenylmethanepyro-mellitamic acid). Density measurements and x-ray diffraction studies were carried out to study the structure of the resultant polyimide fibers. Polyamic acid as well as undrawn polyimide fibers were essentially amorphous with two amorphous haloes. Hot drawing of the fibers at 300°C resulted in increase in crystallinity, and a simultaneous decrease in density also took place. X-ray data revealed that meridional reflections correspond to the repeat unit length in the fiber. Scanning electron micrography studies indicated that polyamic acid fibers prepared by a wet-spinning technique developed voids during spinning which increased on cyclodehydration to the polyimide state. Hot drawing of fibers resulted in enlargement of these voids. However, a highly fibrillated structure was developed during drawing which could account for the strength of the fibers.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 2913-2920 
    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: Radiolysis of poly(vinyl alcohol) fibers (PVA) in the presence of chloroform and carbon tetrachloride was investigated. Decrease in intrinsic viscosity was observed at lower dosages (up to 2.3 megarads); and above this, an increase was noted. The blank samples irradiated under similar conditions showed a continuous decrease in intrinsic viscosity. A discoloration in the samples irradiated in the presence of CCl4 and CHCl3 was also observed. It is attributed to double bond formation in the backbone. A marginal decrease in the tensile strength of the irradiated fibers was observed. However, the surface characteristics of the fibers did not change on irradiation. The thermogravimetric analysis revealed a better heat resistance in irradiated fibers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 1061-1072 
    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: Polyimides were synthesized from 4,4′-diamino diphenyl methane and pyromellitic dianhydride using low-temperature solution polycondensation. Solutions of these polyamic acids in dimethyl-formamide (DMF) were spun into fibers by the wet spinning technique using a mixture of DMF and water as coagulants. Various spinning parameters such as dope concentration, bath composition, and jet stretch were standardized to get polyimide fibers with optimum properties. It was observed that fibers spun at higher jet stretch did not cyclize satisfactorily. Higher dope concentrations gave fibers with better properties. Cyclodehydrated fibers were hot-drawn at 300°C. Fibers with a tenacity of 380 mN/tex, an extension at break of 10%, and initial modulus of 4060 mN/tex were obtained. Mechanical properties of fibers at elevated temperatures, i.e., 100 and 200°C were also measured. Heat aging at 100, 200, and 300°C was carried out for 10 hr. This resulted in an increase in the initial modulus of fibers. However, a 28% decrease in tenacity was observed when the fibers were heat-aged at 300°C. The dynamic thermogravimetry in air showed that fibers were stable up to 400°C. The activation energy of decomposition, calculated from these thermograms in the temperature range 540-610°C was 101 kJ/mole.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 2933-2938 
    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 potential of 2-hydroxyethyl methacrylate and ethyl acrylate copolymers as negative photoresists was studied. Negative photoresist solution was prepared by esterfication of copolymers with cinnamoyl chloride. The effects of photosensitizer concentration, copolymer composition, and exposure time were investigated. A resolution of 30 μm was attained from these photoresists.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 64 (1977), S. 101-113 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyamidsäuren wurden aus Pyromellithsäuredianhydrid und Benzidin (B) sowie Hydrazin (H) dargestellt und druch Viskositätsmessungen in Dimethylformamid (DMF) charakterisiert. Die Hydrolysestabilitßat wurde nach 20tägige Aufewahrung der DMF-Lösungen an der Luft bei Raumtemperatur ermittelt. Es ergab sich eine Viskositätsabnahme für die B-Polymeren und die Copolymeren mit B und H. Diese Verminderung ist für die Copolymeren geringer.Das thermische Verhalten der Polyamidsäuren und Polyimide wurde mittels thermogravimetrischer und differentialthermoanalytischer Methoden untersucht. Die Copolyamidsäuren wiesen eine größere thermische Stabilität als die Polyamidsären aus B auf, während die Copolyimide eine geringere Stabilität als die Polyimide aus B aufwiesen. Die thermische Cyclodehydrierung der Polyamidsäuren zu den polyimiden fand bei den Copolymeren bei geringeren Temperaturen als bei den B-Polymeren statt.
    Notes: The polyamic acids from pyromellitic dianhydride, benzidine (B) and hydrazine (H) were prepared and characterized by intrinsic viscosity measurements in dimethylformamide (DMF) solutions. The hydrolytic stability of these polymers was determined by keeping the DMF solution in presence of air at room temperature for 20 days. A decrease in ηinh was observed for the B-polymers and copolymers of B and H. This reduction was less in the copolymers.The thermal behaviour of polyamic acids and polyimides was studied by thermogravimetric and differential thermal analysis techniques. The copolyamic acids were found to be thermally more stable than polyamic acid from B at higher weight losses (about 50%), whereas copolyimides were found to be less stable than polyimide from B. Thermal cyclodehydration of polyamic acids to polyimide occurred at lower temperatures in copolymers than the polymer of B.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 78 (1979), S. 181-193 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Absorptionsspektrum von in Äthylbenzoat bei 200°C in Anwesenheit von Maleinsäureanhydrid (MA), Benzochinon (BQ) und Anthrachinon (AQ) abgebautem PVC wurde untersucht. Die Polyensequenzlängenverteilung wurde berechnet und festgestellt, daß die Bildung von Polyenen mit 6 konjugierten Doppelbindungen durch MA, nicht hingegen durch BQ und AQ reduziert wird. BQ und AQ verringern aber die Bildung von längeren Polyenen (n=8). Das Alterungsverhalten der abgebauten Polymerproben wird ebenfalls untersucht.
    Notes: Electronic absorption spectra of PVC degraded in ethyl benzoate at 200°C in presence of maleic anhydride (MA), benzoquinone (BQ) und anthraquinone (AQ), were studied. The distribution of polyene sequence length was calculated. It was observed that the rate of formation of polyenes having 6 conjugated double bonds was reduced in presence of MA. In case of BQ and AQ, no such inhibiting effect was observed. However, formation of polyenes having a higher number of double bonds (i. e. n=8) was reduced in the presence of these additives. The ageing behaviour of the degraded polymer samples was also investigated.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 79 (1979), S. 147-155 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Veränderungen der Molekulargewichte und der Molekulargewichtsverteilung von PVC, das in Gegenwart von Maleinsäureanhydrid, Benzochinon oder Anthrachinon abgebaut wurde, wurden durch Gelchromatographie untersucht. Ketten-Spaltungs- und Vernetzungsreaktionen waren durch den M̄w und M̄n-Wert zu erkennen. In Gegenwart von Anthrachinon waren Vernetzungsreaktionen vorherrschend.
    Notes: The changes in molecular weight and molecular weight distribution of PVC degraded in presence of maleic anhydride, benzoquinone and anthraquinone were studied by gel permeation chromatography. Chain scission and crosslinking reactions were indicated on the basis of M̄n and M̄w of degraded samples. Crosslinking was predominant when degradation was carried out in presence of anthraquinone.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 80 (1979), S. 119-127 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zahlreiche Copolymere mit Benzimidazolringen, Alkylen- und Arylengruppen in der Kette wurden aus 3,3′-Diaminobenzidintetrahydrochlorid-dihydrat und Dicarbonsäuren in Polyphosphorsäure hergestellt. Die Viskositätszahlen dieser Polymeren in conc. H2SO4 wurden bei 30, 40 und 50°C bestimmt. Es wurde kein systematischer Gang der Huggins-Konstante mit der Temperatur gefunden. Q- und A-Werte der Gleichung η = A · exp(Q/RT) wurden für diese Polymeren in H2SO4 bestimmt. Aus den A-Werten wurde geschlossen, daß die meisten Polymeren steife Ketten bilden, mit Ausnahme derer, die cis-Vinylengruppen in der Kette enthalten.
    Notes: Various copolymers having benzimidazole rings along with alkylene and arylene groups in the backbone were prepared from 3,3′-diaminobenzidine tetrahydrochloride dihydrate and dicarboxylic acids in polyphosphoric acid. The viscosities of these polymers in concentrated sulphuric acid (98%) have been determined at 30, 40 and 50°C. There is no systematic variation in the value of K′ (Huggins constant) with temperature. Values of Q and A in the expression η = A exp(Q/RT) were obtained for these polymer samples in H2SO4. On the basis of the ‘A’ values, it has been concluded that most of these polymers were stiff chains with the exception of those containing cis-vinylene groups in the backbone.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 82 (1979), S. 63-78 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurden Polyetherterephthalate (PET), die Ethersegmente enthalten, durch Schmelzkondensation unter Verwendung von Dimethylterephthalat (DMT) und unterschiedlichen Mengen von Ethylenglykol (EG) und Polyethylenglykol (PEG) als Ausgangsmonomere hergestellt.Die Charakterisierung der Polymeren erfolgte durch Messungen der Viskosität und der dynamischen Thermogravimetrie in Luft. Der Schmelzpunkt erniedrigte sich von 258°C bis 244°C mit zunehmendem Anteil von Polyethersegmenten in der Polymerkette.Diese Polymeren wurden unter Verwendung der Schmelzspinntechnik zu Fasern versponnen. Die Fasern wurden bis zu unterschiedlichen Verstreckungsverhältnissen verstreckt und dann getempert. Mit der Zunahme der Polyethersegmente im Copolymeren, wurde eine Erniedrigung von ReiRfestigkeit und Anfangsmoduln festgestellt, wahrend sich die prozentuale Dehnung erhohte. Eine optimale Festigkeit wurde mit BL 3 Fasern erzielt, und eine weitere Erhohung von PEG (BL 4) beeinfluRt die Festigkeit und Anfangsmoduln nicht mehr.Die Farbaufnahme und Wasserdampfsorption der Copolyester war deutlich erhoht, verglichen mit PET.Die Kristallinitat und Orientierung wurde durch Rontgenbeugung bestimmt. In den zug- und hitzebehandelten Fasern erniedrigte sich die Dichte mit der Erhohung des PEG-Anteils, dagegen war erwartungsgemaR die Dichte in BL 4 hoher als in PET.
    Notes: Poly(ethylene terephthalate) (PET) having ether segments have been prepared by melt condensation by taking dimethyl terephthalate (DMT) and different quantities of ethylene glycol (EG) and polyethyl'ene glycol (PEG) in the initial monomer feed.The polymers were characterized by intrinsic viscosity measurements. The relative thermal stability of the polymers was evaluated by dynamic thermogravimetry in air. The melting point was found to decrease from 258-244°C with increase of polyethylene oxide segments in the polymer backbone.These polymers were spun into fibres by using melt spinning technique. The fibres were drawn to different draw ratios and then heat-set. With the increase of the mole percentage of polyether segments in the copolymers, a decrease in tensile strength and initial modulus of the fibres was observed while percentage elongation increased. An optimum tenacity was obtained with BL 3 fibres, and further increase of PEG (BL 4) did not affect the tenacity of initial modulus. The dye uptake and moisture regain in copolyesters was greatly enhanced compared to PET. The crystallinity and orientation of fibres was studied by X-ray diffraction pattern. In the drawn and heat set fibres, the density decreased on increasing the PEG content except in BL 4 where the density was higher than in PET.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3279-3289 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several copolymers of 2-hydroxyethyl methacrylate (HEMA) with methyl acrylate (MA), ethyl acrylate (EA), n-butyl acrylate (BA), and methyl methacrylate (MMA) were prepared at 70°C in nitrogen atmosphere using 0.2% (w/v) benzoyl peroxide as initiator. The copolymer composition was evaluated by estimation of hydroxyl group in the copolymers. Intrinsic viscosity of HEMA-EA, HEMA-BA, and HEMA-MMA copolymers was determined at 35°C in dimethyl formamide. Molecular weight distribution of copolymer samples was evaluated by gel permeation chromatography. Thermal behavior of the copolymers was investigated by dynamic thermogravimetry. Thermal stability decreased on increasing HEMA content in MA, EA, and BA copolymers. However, a reverse trend was observed in HEMA-MMA copolymers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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