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  • 1990-1994  (19)
  • Chemistry  (15)
  • Life and Medical Sciences  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2953-2960 
    ISSN: 0887-624X
    Keywords: benzobisthiazole ; bicyclo[2.2.2]octane ; rigid-rod ; colorless ; 3-dimensional ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polycondensation in polyphosphoric acid of 2,5-diamino-1,4-benzene dithiol dihydrochloride with bicyclo[2.2.2]octane-1,4-dicarboxylic acid, as well as the corresponding dimethyl ester or diacid chloride, led to rigid-rod benzobisthiazole polymers. Colorless and soluble polymers with intrinsic viscosities as high as 30.6 dL/g (methanesulfonic acid, 30°C) were obtained. The ultraviolet-visible spectrum of a polymer film cast from methanesulfonic acid under reduced pressure displayed no absorptions in the visible range (400-900 °m). The polymer was thermooxidatively stable up to 420°C in air as determined by thermogravimetric analysis. Fibers spun from a lyotropic polyphosphoric acid solution exhibited a tensile strength of 300-450 Ksi, a modulus of 26 Msi, and a compressive strength of 53 Ksi. Wide-angle X-ray scattering patterns of polymer fibers indicated a 3-dimensional crystal structure rather than a nematic liquid crystal structure. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 407-418 
    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 population-balance-equation model is employed for the analysis of liquid-liquid extraction columns. This model considers drop breakage, coalescence, and exit phenomena for the drop phase caused by drop-drop and drop-continuous phase interactions. Drop breakage and coalescence rates are employed from a previous study on liquid dispersions in stirred-tank contactors. A drop exit frequency is developed based on a stochastic modeling approach. The model is tested by drop size distribution and dispersed-phase volume fraction (holdup) data obtained for a multistage column contactor of pilot-plant scale. Steady-state drop size distribution and transient holdup measurements are obtained by a photomicrographic technique and an ultrasonic technique, respectively. The model can predict flooding of the column. The effect of mass transfer on the hydrodynamic parameters of the contactor is also examined. The population-balance-equation model can be used for the control of extraction columns and can be extended to include mass-transfer calculations for the prediction of extraction efficiency.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 419-423 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Three-dimensional Stokes flow through a thin screen which has a regular array of holes with two orthogonal axes of symmetry has been studied. The governing equation is simplified by the Roscoe potential and solved by an efficient eigenfunction expansion and collocation method. The resistance is found for circular and square holes in square arrays, and circular and hexagonal holes in triangular arrays.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 4 (1992), S. 84-90 
    ISSN: 0899-0042
    Keywords: high-performance liquid chromatography (HPLC) ; chiral assay ; naproxen chloride ; pharmacokinetics ; racemate ; stereoselective ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A stereospecific high-performance liquid chromatographic (HPLC) method was developed for the quantitation of the enantiomers of venlafaxine, an antidepressant, in dog, rat, and human plasma. The procedure involves derivatization of venlafaxine with the chiral reagent, (+)-S-naproxen chloride, and a postderivatization procedure. The method was linear in the range of 50 to 5,000 ng of each enantiomer per ml of plasma. No interference by endogenous substances or known metabolites of venlafaxine occurred. Studies to characterize the disposition of the enantiomers of venlafaxine were conducted in dog, rat, and human, following oral administration of venlafaxine. The Cmax, area under the curve (AUC) and (S)/(R) concentration ratios of the (R)- and (S)-enantiomers were compared. In rats, the mean plasma ratio of (S)-venlafaxine to that of (R)-venlafaxine over 0.5 to 6.0 h varied from 2.97 to 8.50 with a mean value of 5.51 ± 2.45. The Cmax, AUC0 - ∞, and t1/2 values of the (R)- and (S)-enantiomers in dogs were not significantly different from one another (P〉0.1). The mean ratios [(S)/(R)] of enantiomers of venlafaxine in human over a 2 to 6 h interval ranged from 1.33 to 1.35 with an overall ratio of 1.34 ± 0.26 (n = 12). These ratios of the enantiomers [(S)/(R)] were not statistically different from unity (P〉0.1) indicating that the disposition of venlafaxine enantiomers in humans is not stereoselective and is more similar to that in dogs than that in rats.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 81-84 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new nicotine sensor for the simple, rapid determination of nicotine in tobacco products without prior separation is described. The sensor is a coated graphite electrode with silicotungstic acid as the active material in polyvinyl chloride with di(2-ethylhexyl) phthalate as the plasticizer. At pH 5.5-6.0, it provides a Nernstian response to nicotine over 10-1 to 10-6 M; the detection limit is 7.4 × 10-7 M, and the average slope is 58 mV/pN. The analytical recovery is 98.1 to 102.3%. Satisfactory results are obtained in comparison with silicotungstate gravimetric method and UV spectrometry.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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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: We have used the molecular dynamics (MD) simulation package AMBER4 to search the conformation of a peptide predicted as a leucine zipper motif for the human immunodeficiency virus type I integrase protein (HIV IN-LZM). The peptide is composed of 22 amino acid residues and its location is from Val 151 to Leu 172. The searching procedure also includes two known α-helices that served as positive controls - namely, a 22-residue GCN4-p1 (LZM) and a 20-residue poly(L-alanine) (PLA). A 21-residue peptide extracted from a cytochrome C crystal (CCC-t) with determined conformation as a β-turn is also included as a negative control. At the beginning of the search, two starting conformations - namely, the standard right-handed α-helix and the fully stretched conformations - are generated for each peptide. Structures generated as standard α-helix are equilibrated at room temperature for 90 ps while structures generated as a fully stretched one are equilibrated at 600 K for 120 ps. The CCC-t and PLA helices are nearly destroyed from the beginning of equilibration. However, for both the HIV IN-LZM and the GCN4-p1 LZM structures, there is substantial helicity being retained throughout the entire course of equilibration. Although helix propagation profiles calculated indicate that both peptides possess about the same propensity to form an α-helix, the HIV IN-LZM helix appears to be more stable than the GCN4-p1 one as judged by a variety of analyses on both structures generated during the equilibration course. The fact that predicted HIV IN-LZM can exist as an α-helix is also supported by the results of high temperature equilibration run on the fully stretched structures generated. In this run, the RMS deviations between the backbone atoms of the structures with the lowest potential energy (PE) identified within every 2 ps and the structure with the lowest PE searched in the same course of simulation are calculated. For both the HIV IN-LZM and the GCN4-p1 LZM, these rms values decrease with the decrease of PE, which indicates that both structures are closer in conformations as their PEs are moved deeper into the PE well. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 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 28 (1990), S. 963-971 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diffusion coefficients of camphorquinone (CQ) and its photoproduct (CQP) in two poly(methyl metbacrylate) (PMMA) samples with different molecular weights are measured as a function of temperature. Above the glass transition, the temperature dependence is not Arrhenius and can be described by the Williams-Landel-Ferry equation. It is also shown that the difference in the temperature dependence of the diffusion coefficients of CQ in the two PMMA samples is attributable to the difference in glass transition temperatures.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2615-2624 
    ISSN: 0887-6266
    Keywords: second harmonic generation ; correlated dipolar orientation ; trapped charges ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Second harmonic generation (SHG) in three corona-poled, pure, bulk polymers is studied as a function of temperature. It is found that this technique readily yields dynamical information that is complementary to that obtained from the technique of dielectric relaxation (DR). The SHG results are compared to those from DR in the same temperature ranges above Tg. It is found that in the temperature ranges examined, the relaxation times obtained from SHG are several orders fo magnitude longer than those measured by dielectric relaxation. This is explained as being due to the strong correlation between oriented dipoles and to trapped charges injected by the poling process. Fitting measured data to the Williams-Landau-Ferry (WLF) equation indicates that more free volume is needed in SHG for dipolar reorientation than is needed in DR. An SHG relaxation elongation phenomenon at constant temperature is found to occur in the pure bulk polymers and is similar to that found in chromophore-doped polymers previously studied. The SHG technique is developed as a new tool to directly study the reorientational dynamics of polar polymer segments. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1799-1807 
    ISSN: 0887-6266
    Keywords: ion implantation ; rigid-rod polymer ; poly(p-phenylene benzobisthiazole) ; poly(p-phenylene benzobisoxazole) ; rigid-rod pseudo-ladder polymer ; poly(p-(2,5 dihydroxy) phenylene benzobisthiazole) ; poly(p-(2,5-dihydroxy) phenylene benzobisoxazole) ; poly(p-(2,5-dihydroxy) phenylene benzobisimidazole) ; ladder polymer ; poly(benzimidazobenzophenanthroline) ; electrical conductivity ; molecular structure effect ; molecular orientation effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isotropic and oriented thin films of rigid-rod, rigid-rod pseudo-ladder, and ladder polymers were ion-bombarded with 84Kr+ to a dose of 4 × 1016 ions/cm2. The bombardment was conducted at two conditions: one at 190 keV energy with 0.12 μA/cm2 current density and the other at 200 keV energy with 2.0 μA/cm2 current density. With the low current density, the polymers developed a uniform ion-bombarded layer of about 0.35 μm at the surface. This layer showed an electrical conductivity on the order of 10-3s/cm at ambient conditions, an enhancement of 6 to 9 orders of magnitude from the pristine polymers. The enhanced conductivity was found to decrease to 10-6s/cm after the implanted krypton was removed by heating under reduced pressure. It suggests that the enhanced conductivity was due to a synergistic effect of structural change of the polymers and chemical doping by the im-planted ions. With the high current density, most polymer films, except that of rigid-rod pseudo-ladder poly(p-(2,5-dihydroxy) phenylene benzobisthiazole) (DPBT), developed an additional fibrous network structure over the uniform ion-bombarded layer. The comparable conductivity, 53 to 157 s/cm, measured for the various ion-bombarded films in-dicated that neither the molecular structure, rigid-rod or ladder, nor the molecular packing order, isotropic or oriented, constituted significant effect on the conductivity of ion-bombarded polymers. Since krypton could not be detected in the polymers ion-bombarded with high current density, the enhanced conductivity was attributed to the structural change of the polymers. The DPBT films ion-bombarded with high current density showed holes of micron size, probably due to the decomposition of hydroxy pendents from the rigid-rod backbone. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1437-1442 
    ISSN: 0887-6266
    Keywords: polycarbonate ; orientation ; anisotropic diffusion ; stretched film ; strain rate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Employing the laser-induced holographic grating relaxation technique, we have measured tracer diffusion coefficients of a phtochromous dye, camphorquinone, in uniaxially drawn polycarbonate films as a function of stretch ratio. Anisotropy in the tracer diffusion coefficient has been observed with D∥ greater than D⊥ by at least a factor of 4 for the film stretched to the stretch ratio δ = 2.3. The diffusion coefficient along the direction of stretch D∥ increases significantly with increasing δ, whereas D⊥ decreases slightly with increasing δ. The stretch ratio dependence of D∥ and D⊥ is interpreted according to a modified free volume theory. The strain rate and stretch temperature dependence of the anisotropic tracer diffusion coefficient has also been investigated. © 1992 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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