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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 173-196 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Miyazawa-Blout-Krimm (M-B-K) treatment of polypeptide absorption in the infrared is extended to the calculation of circular dichroism (CD), linear dichroism, and oriented CD for the amide I and amide II transitions. Matrix methods are applied to the α helix and β structures using measured values for the strengths and directions of the transition dipole moments and empirical values from M-B-K for the coupling constants.Relatively small aggregates, a 36-residue helix, and 8-chain × 4-residue β sheets, are large enough to show calculated absorption agreeing with M-B-K results, which are based on infinite lattices.In all cases the predicted CD is an approximately conservative couple. The strongest CD should appear in the α helix, Δε/ε ≃± 10-3 for both transitions. The amide II transition should show moderate CD couples in both β structures, Δε/ε ≃ (+2 to -1) × 10-4. The amide I transitions in β structures should show weak CD couples, Δε/ε = (+3 to -2) × 10-5, except that the negative branch in the antiparallel structure may be detectable (Δε/ε ≃ -2 × 10-4) because absorption is very low at its wavelength peak.CD on oriented samples should be enhanced over the unoriented cases, giving values as large as Δε/ε = 3 × 10-3 because particular directions of observation allow the light to avoid much of the absorption in the sample.If all three structures are considered as helices, then the larger distance of the transition dipoles from the axis in the α helix, and the orientations of the transitions in the different structures, are the factors that, in terms of our previous theoretical work [Snir and Schellman (1973) J. Phys. Chem. 77, 1653] satisfactorily explain the calculated results. Simple dipole-dipole interaction is calculated to make a substantial contribution to the coupling between groups.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3383-3388 
    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 interfacial polymerization technique was used in the preparation of organotion polyesters. Dialkyltin dihalides dissolved in an organic solvent immiscible with water were reacted with the dialkali metal or ammonium salt of a dicarboxylic acid. High yields of polyesters were obtained after short reaction times. The polyesters were generally insoluble and were high melting. Copolymers were also obtained.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 38 (1992), S. 535-543 
    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 hybrid model is developed and implemented for predicting the limiting bound of the reactant conversion rate in an isotropic turbulent flow under the influence of a reaction of the type A + B Products. This model is based on the amplitude mapping closure of Kraichnan for the molecular mixing of a stochastically distributed scalar, and the eddy-damped quasi-normal Markovian (EDQNM) spectral closure for the two-point scalar covariance. The results predicted by this model compare well with available experimental data in both gaseous and aqueous plug-flow reactors, but point to the need for more detailed measurements in future experimental studies. With the implementation of the mapping closure, a simple analytical expression is obtained for the decay rate of the unmixedness. This expression is very convenient and is recommended for direct practical applications in the modeling and design of plug-flow reactors.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 899-903 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 258-266 
    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 linear eddy model (LEM) is used for statistical predictions of stationary, homogeneous turbulent flows under the influence of isothermal chemical reactions. Nonpremixed reacting systems are considered with two reaction mechanisms: a binary, irreversible single-step reaction A + B ↦ P; the series-parallel reaction A + B ↦ R, A + R ↦ P. In both systems, the influence of various flow parameters on the reactant conversion rate is elucidated. For the second reaction scheme, effects of the flow parameters on the “selectivity” are also investigated. The trends predicted by the LEM agree with those produced previously by direct numerical simulation (DNS) at moderate values of the Reynolds number, Schmidt number and Damköhler number. An important feature of the LEM is its capability to extend the parameter range well beyond that currently attainable by DNS. The LEM generated results for a wide range of Schmidt and Damköhler numbers are discussed as well as their effects on the selectivity. These results assess the performance of some of the existing closures for modeling of the selectivity. None of the closures are capable of reproducing the LEM results.
    Additional Material: 14 Ill.
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  • 6
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerizations of the N-carboxyanhydrides of 1-aminocyclopropanecarboxylic acid, 1-aminocyclobutanecarboxylic acid, 1-aminocyclopentanecarboxylic acid, and 1-aminocyclohexanecarboxylic acid were investigated. These N-carboxyanhydrides did not polymerize in bulk when heated to their melting points under reduced pressure. In solution, they polymerized extremely slowly on initiation with n-hexylamine and relatively slowly when initiated by sodium methoxide-methanol. The polymerization rates of the above NCAs in dimethyl sulfoxide solution, initiated by sodium methoxide-methanol were found to increase in the following order: NCA of 1-aminocyclohexanecarboxylic acid, NCA of 1-aminocyclopropanecarboxylic acid, NCA of 1-aminocyclopentanecarboxylic acid and NCA of 1-aminocyclobutanecarboxylic acid. The influence of the alicyclic side rings on the relative rates of polymerization of the respective NACs is considered.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 396-401 
    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: This paper describes an investigation into some fundamental aspects of ultrasonic welding of thermoplastics. A simple model was developed to characterize the temperature rise at the weld interface up to the glass transition temperature. Beyond this point, the temperature increases more rapidly and almost directly proportional to weld time. The rate of temperature rise increases with increase of amplitude of vibration. The correlation between weld strength and interface temperature was established using the method of dimensional analysis. It was found that the process can be optimized in terms of weld strength by monitoring the power input. There is an optimal load one can apply to achieve high weld strength. The overall efficiency of the process is rather low in terms of energy usage.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 387-394 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low and atmospheric pressure polymerizations of ethylene using catalysts prepared from n-butyl lithium or isoamyl lithium and titanium tetrachloride were studied. The efficiency of the catalyst depended on the molecular ratio of the alkyl lithium to titanium tetrachloride. Optimum molecular ratio for the n-butyl lithium-titanium tetrachloride was found to be between 2.15-2.47 with a sharp drop between 2.15-1.49; for the isoamyl lithium the optimum was between 2.5-4.3. Within the examined interval (of atmospheric pressure to a pressure of 60-70 lb./sq. in.) higher pressure caused an increase in the yield of polyethylene. No pronounced effect in polymerization was found in the temperature interval of -10-55°. The catalyst is stable for a few days if kept refrigerated. Petroleum ether, b.p. 40-80°, was the best solvent both for the preparation of the catalyst and for the polymerization. Ligroin, toluene, and especially ether interfered with the polymerization. The polyethylenes obtained melted between 125-135°.
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 39 (1959), S. 347-356 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low pressure polymerization of ethylene by use of catalysts prepared from either butyl or amyl potassium, or the reaction product of potassium with chlorobenzene and titanium tetrachloride was studied. The efficiency of the catalysts depended on the molar ratio of the potassium alkyl to titanium tetrachloride but was in every case considerably lower than that of the corresponding lithium or sodium alkyl containing catalysts. Optimum molar ratios of the butyl potassium-titanium tetrachloride catalysts were between 2.8 to 6.1 with sharp drops on both sides of the optimum; for the amyl potassium between 1.1 to 3.7. The reaction product of potassium with chlorobenzene yielded much weaker catalysts with titanium tetrachloride, and the properties of the polymers obtained were different. The physical properties of the polyethylenes obtained, as determined from x-ray diffraction diagrams, infrared spectra, and from melting points, showed similarity to those obtained with the lower alkali metal catalysts. The lower activity of the potassium catalysts may be related to the large ionic radius of the potassium, which influences the properties of the catalyst complex formed with titanium tetrachloride. Propylene did not undergo polymerization with the potassium alkyl containing catalysts at low pressure.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 40 (1959), S. 149-158 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low pressure polymerization of propylene was investigated using catalysts prepared from alkali metal alkyls and titanium tetrachloride. In all cases the efficiency of the catalysts depended on the molecular ratio of the metal alkyl to the titanium tetrachloride. In general the polymerization conditions were similar to those for ethylene although the propylene polymerized much more slowly. With n-butyllithium-titanium tetrachloride, optimum molecular ratios were found between 1.8-2.5, with sharp drops on both sides. With amylsodium-titanium tetrachloride the optimum extended over a wide range (5.7-15), the activity decreasing sharply with lower molecular ratios. The catalysts prepared from sodium alkyls were more active than those prepared from lithium alkyls. Increasing yield was obtained on lowering the concentration of the catalyst. Up to a pressure of about 3 atmospheres, increase in the rate of polymerization was observed with increase in pressure; above this no influence of the pressure was observed. Isotactic polymers were isolated from the polymerization products by successive fractionation of the crude polymers in acetone, ether, and isooctane which dissolved the atactic polymers. With butyllithium-titanium tetrachloride catalysts, at and above optimum ratios, the isotactic fractions were about 60%. At lower ratios there was a great increase in atactic polymers. With amylsodium-titanium tetrachloride catalysts the isotactic fractions were about 70%. Phenylsodium-titanium tetrachloride catalysts were found to be very weak in the polymerization of propylene.
    Additional Material: 3 Ill.
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