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  • 2020-2024
  • 1990-1994  (8)
  • 1992  (8)
  • Polymer and Materials Science  (7)
  • Candida blankii  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 479-484 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of industrial microbiology and biotechnology 9 (1992), S. 109-113 
    ISSN: 1476-5535
    Keywords: Candida blankii ; Biomass ; d-Xylose ; l-Arabinose ; Acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary All fourCandida blankii isolates evaluated for growth in simulated bagasse hemicellulose hydrolysate utilized the sugars and acetic acid completely. The utilization ofd-xylose,l-arabinose and acetic acid were delayed by the presence ofd-glucose, but after glucose depletion the other carbon sources were utilized simultaneously. The maximum specific growth rate of 0.36 h−1 and cell yield of 0.47 g cells/g carbon source assimilate compared with published results obtained withC. utilis. C. blankii appeared superior toC. utilis for biomass production from hemicellulose hydrolysate in that it utilizedl-arabinose and was capable of growth at higher temperatures.
    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 30 (1992), S. 2735-2747 
    ISSN: 0887-624X
    Keywords: alternating copolymerization ; ethylene-carbon monoxide polymers ; palladium catalysis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new [(PPh2CH2CH2CH2PPh2)Pd(CH3CN)2](BF4)2/CH3OH catalyst for olefin/carbon monoxide alternating copolymerization has been found which is far more active and more stable than previous monodente phosphine Pd catalysts. Methanol is a coinitiator as well as a chain transfer agent. Protonic acid is not a coinitiator but causes chain transfers. In the absence of methanol, the copolymerization was characterized by long induction period and slow rate © 1992 John Wiley & Sons, Inc.
    Additional Material: 11 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 30 (1992), S. 1899-1909 
    ISSN: 0887-624X
    Keywords: spiro(benzoxasilole) ; oxetane ; catalysis ; polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A spiro(benzoxasilole) catalyst, 3,3,3′,3′-tetrakis(trifluoromethyl)-1,1′-(3H,3H′)-spirobis(1,2-benzoxasilole) was used to polymerize 3,3-R,R′-oxetanes: BEMO (R, R′ = ethoxymethyl), AMMO (R = azidomethyl, R′ = methyl), NMMO (R = nitratomethyl, R′ = methyl), BAMO (R, R′ = azidomethyl), and BCMO (R, R′ = chloromethyl) with descending rates in this order. 31P-NMR of polymerization mixtures quenched using Bu3P are consistent with an oxonium ion propagating species. Water is not a cocatalyst because it increases the induction period which is not eliminated by the proton trap 2,6-di-t-bu-tylpyridine. The propagating chains were terminated by transfer with the ether oxygen of the polymer either intermolecularly or intramolecularly. The index of propagation to chain transfer, Kkikp/ktr, varies over more than three orders of magnitude for BEMO 〉 AMMO 〉 NMMO 〉 BAMO. However, kp/ktr for the four monomers differ by less than a factor of five indicating the same factors are affecting propagation and chain transfer. Addition of benzyl alcohol and propandiol produced poly(BEMO) having one and two hydroxyl termini, respectively. These telechelic polymers can be used to synthesize linear triblock or multiblock copolymers of oxetane derivatives. © 1992 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0887-624X
    Keywords: Ziegler-Natta catalysts ; ansa-metallocene catalyst ; thermoplastic elastomeric poly(propylene) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Racemic-anti-[ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dimethyltitanium (6) has been synthesized and its molecular structure determined by x-ray diffraction methods. The two Ti=Me(1) and Ti=Me(2) units have bond distances differing by 0.08 Å and their proton NMR resonances are separated by over 1 ppm. Using this compound and methylaluminoxane (MAO) as the activator, at 25°C the 6/MAO catalyst produced polypropylene having crystalline domain with physical crosslinks. The polymers obtained at lower polymerization temperatures are rheologically liquids. The behaviors of this catalyst system resembles closely the previously reported rac-[anti-ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dichlorotitanium (4)/MAO system. The structure of 6 determined here furnishes tangible support for the proposed two-state (isomeric)-switching propagation mechanism. Addition of MAO to 6 causes broadening of the Me(1) resonance in the 1H-NMR spectra, and 6 is decomposed by Ph3C+B(C6F5)-4. © 1992 John Wiley & Sons, Inc.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 1603-1611 
    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: Linear ABA triblock and (AB)n segmented block copolymers of energetic monomers have been synthesized. The rigid and soft blocks are prepared from 3,3-bis(azidomethyl)oxetane (BAMO) and 3-nitratomethyl-3-methyloxetane (NMMO), respectively. Polymerization of BAMO initiated by triethyloxonium tetrafluoroborate and by spiro(benzoxasilole)/propanediol produced α,ω-monohydroxy-PBAMO (3) and α,ω-dihydroxy-PBAMO (4) of M̄n 16,000 and 2,000, respectively, and α,ω-dihydroxy-PNMMO (5) of M̄n = 13,000 was synthesized by the latter method. The block copolymers were prepared from the appropriate telechelic polymers and toluene diisocyanate. The PBAMO - PNMMO - PBAMO copolymer 6 has Tm = 82°C, Tg = -3°C, and is strongly phase separated even in the melt. It decomposes sharply within 1°C at 224°C evolving 0.69 kJ/g of heat. Copolymer 6 has excellent mechanical properties with elongation of 683% at break, 5.25 MPa stress, and 82% recovery. The (PBAMO - PNMMO)n copolymer 7 has similar thermal properties and spectroscopic characteristic, but is inferior to copolymer 6 in all rheological and mechanical properties. © 1992 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 455-463 
    ISSN: 0887-6266
    Keywords: degradation kinetics, model equation for multiple reaction mechanisms in ; polyether-ether-ketone (PEEK), model for predicting isothermal degradation kinetics of ; thermal degradation of polymers, generalized model for kinetics of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A composite degradation methodology is extended to the conversion-dependence function in order to explain the importance of multiple reaction mechanisms which might be considered to be involved in degradation processes. Based on two elementary reaction mechanisms, a specific form of the model equation is derived, which is capable of describing various types of degradation behavior showing sigmoidal rate as well as deceleratory rate. The conversion-dependence function is derived to be independent of the Arrhenius-type reaction constant or temperature, and thus the kinetic parameters are determined by analytic methods that have been developed for isothermal and dynamic-heating experiments without any modification or additional assumptions. The developed model equation is tested by predicting the isothermal master curve of polyether-ether-ketone (PEEK), which is used as a model system in this study. The activation energies of the model system are analyzed using comparable methods for isothermal and dynamic experiments, which compare favorably in terms of the activation energy as a function of conversion. The resulting model equation, based on the kinetic parameters determined by isothermal experiments, can accurately predict both isothermal and dynamic-heating thermogravimetry utilizing the same constants and identical reaction mechanisms without additional assumption.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 41-53 
    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: Poly(amide imide) (PAI) has proven to be an excellent engineering thermoplastic. Injection and compression molding processes are currently used to produce poly(amide imide) parts when superior toughness, solvent resistance, and high-temperature heat performance are required. The objective of this work was to determine the essential features necessary to use these systems as matrices for carbon-fiber-reinforced composites. The principal steps utilized were: impregnation of the carbon fibers with a PAI solution, drying the solvent from the individual plies, stacking the plies for final consolidation, and a postcure. A processing cycle was developed applicable to resins with different solvent concentration and molecular weight, giving special attention to the solvent evaporation step. A model capable of predicting the rate of evaporation as a function of temperature was developed using the principle of time-temperature superposition. A viscosity model similar to that for a curing thermoset was developed by combining Arrhenius expressions for the temperature and concentration effects. Collectively, this work then provided insight for matrix requirements in the formulation of PAI composites by solvent impregnation.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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