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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 463-472 
    ISSN: 0009-2940
    Keywords: Hypervalent compounds ; Tellurium ; Polycations ; Molecular Orbital Theory ; Band structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Approximate MO and band structure calculation are used to analyze the bonding in the recently synthesized paramagnetic, semiconducting phase [Te15Br4]2+. The [Te15Br4]2+ chains are very similar to those in the tellurium subhalide Te2Br. The electronic structure and bonding within these chains is analysed and the possibility of hypervalency in both [Te15Br4][MoOBr4]2 and Te2Br is discussed. The bonding in the classically hypervalent molecule TeBr42- and a model Te3Br24- is compared to that of the infinite system. Our calculations indicate that both [Te15Br4][MoOBr4]2 and Te2Br contain weakly hypervalent Te atoms and that the interesting electronic properties of [Te15Br4][MoOBr4]2 arise within the distinct sublattices, which do not interact significantly.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1583-1588 
    ISSN: 0009-2940
    Keywords: Alkylidyne ligands ; Carbon-carbon coupling ; Tungsten complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of the alkylidyne complexes [W(CR)Br(CO)3L] [2b (L = CO; R = C6H4-OMe-4), 2c (L = CO, R = C6H4-NMe2-4), 3a (L = PPh3; R = Ph), and 3c (L = PPh3; R = C6H4-NMe2-4)] with methyllithium in THF at -78°C affords the alkylidyne acyl tungsten complexes Li[W(CR)(COMe)Br(CO)3L] [4b (L = CO; R = C6H4-OMe-4), 4c (L = CO, R = C6H4-NMe2-4), 5a (L = PPh3; R = Ph), and 5c (L = PPh3; R = C6H4-NMe2-4)]. Reaction of complexes 4 and 5 with C2O2Br2 at -78°C-0°C in CH2Cl2 followed by addition of PPh3 gives the alkyne complexes [WBr2(CO)(CH3C = CR)(PPh3)2] (6). The formation of the alkyne ligands in complexes 6 may be considered as the result of formal coupling of two alkylidyne ligands.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 587-595 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: An engineering equation that describes the steady shear viscosity of polystyrene melts is developed as an extension of the well known power law model for non-Newtonian viscosity. The parameters in the equation have been related to weight and number averaged molecular weights and temperature. The model is tested on data for both narrow and broad molecular weight polystyrenes whose properties span most materials of commercial importance. This equation predicts the melt viscosity-shear rate behavior for both narrow and broad distribution polystyrenes from knowledge of weight and number averaged molecular weights and temperature. Our analysis directly yields shift factors for the shear rate and viscosity axes. Therefore, no secondary calculations are necessary to generate master curves for polystyrenes. The shift factors are related to weight and number averaged molecular weights of the polystyrenes and temperature of the melt.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3575-3585 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A surfactant bis[2-(10-undecenoyloxycarbonyl)ethyl] (p-vinylbenzoyl) methylammonium chloride formed a lamellar liquid crystal in native form and retained the structure after polymerization. Addition of heptadiene, of glycerylmonomethacrylate, and of both to the surfactant monomer gave an isotropic solution, which was transformed to a lamellar liquid crystal after polymerization. Low angle X-ray diffractometry was used to determine the interlayer spacing and to estimate the location of the added molecules. 1.6-Heptadiene was located between methyl group layers of the surfactant chains with 46 vol % of the molecules penetrating between the hydrocarbon chains of the surfactant. Addition of both the polar and the nonpolar monomer followed by polymerization caused the latter to be expelled from the space in between the chains.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 1105-1124 
    ISSN: 0887-624X
    Keywords: liquid crystalline ; epoxy ; kinetic ; curing ; smectic ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The curing kinetics of a system containing 4,4′-diglycidyloxy-α-methylstilbene (DOMS) and different functionality amines, N-ethylaniline (NEA), aniline, benzenesulfonamide (BSA), and sulfanilamide (SAA), have been studied by differential scanning calorimetry (DSC) under isothermal conditions. The phase transformations during curing of the systems have been monitored by a crosspolarized optical microscope equipped with a hot-stage and photo detector. It has been found that the growth of a nematic liquid crystal structure does not cause a discrepancy from the autocatalytic model for the reactions between aniline and epoxy. There is no liquid crystalline structure formed for the systems containing NEA or BSA, which follow the autocatalytic kinetic models within the temperature range of 120-150°C. For the curing reactions between DOMS and SAA, there is a big deviation from the autocatalytic model when the liquid crystals transfer from a nematic structure to a smectic structure. Unlike the usual decrease of reaction rate resulting from diffusion in a heterogeneous reaction, the reaction rate is enhanced. A modified kinetic model has been constructed for this reaction system by introducing a pseudoconcentration term caused from the liquid crystalline structure formation. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1105-1124, 1997
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1457-1471 
    ISSN: 0887-624X
    Keywords: epoxy ; catalyst ; liquid crystalline ; kinetic ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetraalkylphosphonium-Tetrafluoroborate-Tetrafluoroboric Acid was used as a catalyst in the curing of a liquid crystalline epoxy. Under some conditions the Tetraalkylphosphonium-Tetrafluoroborate-Tetrafluoroboric Acid actually retarded the reaction. An extensive experimental and kinetic analysis is presented anda mechanism for the reaction retardation is proposed. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1457-1471, 1998
    Additional Material: 16 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 473-477 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: No Absract.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 202-214 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A single-pellet reactor has been used to investigate the impact of partial external wetting on catalyst performance in a multiphase reaction system. The novel design simulates the local environment within a trickle-bed reactor, and permits the direct measurement of the degree of wetting under reaction conditions. Experimental data of the hydrogenation of α-methylstyrene (AMS) over a Pd/Al2O3 pellet provide unequivocal evidence of effectiveness enhancement by partial wetting, a predicted single-pellet phenomenon (e.g., Harold and Ng, 1987; Funk et al., 1988, 1989). The overall reaction rate is an increasing (decreasing) function of the degree of wetting if the overall limiting reactant is more effectively supplied through the wetted (nonwetted) part of the surface. A maximum in the reaction rate can occur at an intermediate degree of wetting, signaling a transition from an overall AMS-limited to hydrogen-limited reaction. The dependence of the degree of wetting on the liquid flow rate for low reaction rates is consistent with a simple rivulet flow model. At higher reaction rates the degree of wetting decreases, with all other conditions fixed. Possible mechanisms for this interesting link between the degree of wetting and reaction are discussed.
    Additional Material: 14 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 420-430 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The blown film process has been modeled through the transition from liquidlike to solidlike behavior at the freeze line. A new constitutive equation has been developed that, when incorporated into the the kinematic and dynamic equations that describe the process, for the first time yields qualitatively correct predictions of all process variables. It is suggested that the demarcation between liquidlike behavior and solidlike behavior be altered from the conventional, kinematically based constraint, dr/dz = O, to a rheologically based constraint, the plastic-elastic transition (PET). The results are qualitive in nature since the material is modeled as an elastic solid above the PET instead of as a viscoelastic material. The model is tested using the polystyrene data of Gupta (1981).
    Additional Material: 8 Ill.
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