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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 897-933 
    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: Cast linear polyethylene films subjected to dry and solvent annealing display markedly different sorption and difusion barrier properties than do untreated films. The subsequent sorption of liquid o- and p-xylene and cis- and trans-acetylene dichloride per unit volume of amorphous polymer increases as the annealing temperature and/or treating solvent concentration increases. Integral diffusivities calculated from sorption and steady-state permeation rates show a monotonic increase with sorption per unit volume of amorphous polymer. The concentration dependence, however, is less marked than observed in similar systems at low permeant activity. Apparently the above treatment reduces the effective crosslinking imposed by the crystallites on the amorphous polymer chains through disentangling and incorporating some of these chains into crystallites. Thus the polymer is capable of a greater degree of swelling when brought into contact with a compatible liquid in a spite of a higher degree of crystallinity. The low concentration dependence of the diffusivities is probably due to heterogeneous distribution of excess permeant in a treated film. If the excess permeant were preferentially sorbed in regions of low polymer concentration then the above observations could be explained. Long-duration, osmotic stress-induced swelling and recrystallization have been cited to account for time-dependent permeation rates in treated and untreated films.
    Additional Material: 15 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 331-344 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A quantitative analysis has been made of sorption isotherms and of diffusion data obtained with benzene, acetone, and methanol in ethyl cellulose. The concentration range covered was for volume fractions of penetrant not above 0.1. In this range reproducible measurements were possible. The sorption data show significant departures from the lattice theory of solution. In particular, isotherms tend to curve in the same sense as the Langmuir isotherm; heats of dilution are exothermal; and entropies of dilution are negative. The sign of heats of dilution and the isotherm shapes can be explained if gaps in the polymer provide sorption sites, but the entropy values cannot. An additional ordering or immobilization of the structure around the site, or of penetrant molecules on it, is required. In all these effects it is the nonpolar molecule benzene which shows them most clearly. Diffusion coefficients, D, Arrhenius energies of activation, Ea, and the coefficients D0 in the equation D = D0 exp { -Ea/RT} all depend upon the molecular dimensions of the penetrant. The permeability and D change as the concentration of penetrant increases, except for methanol. These and other aspects of diffusion have been discussed, and compared with results obtained in other polymers.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. 261-275 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The permeabilities and diffusion coefficients of propane, n-butane, and isobutane in stretched peroxide-cured natural rubber have been measured at simple elongations of 0 to 400% in the temperature range 30 to 50°C. To minimize the effect of penetrant on the degree of crystallinity, only regions of low penetrant concentration were chosen. At elongations not sufficient to induce crystallization the permeability did not alter significantly on stretching. At higher elongations the permeability decreased with increasing crystallization. Over a long period of time and at a given temperature the permeability of a crystalline membrane decreased slowly toward an equilibrium value. No such behavior was observed with noncrystalline membranes either stretched or unstretched. Part of the decrease is accounted for by a corresponding slow increase with time in the degree of crystallinity and the remainder is attributed to a partial reorientation or redistribution of the crystallites as the system tends toward an equilibrium state. The data are analyzed in terms of a model in which the crystalline rubber is presented as a rectangular array of small cylindrical crystallites impermeable to penetrant and embedded in an amorphous matrix. To a first approximation the dependence of the permeability on crystallinity and temperature is represented satisfactorily by expressions based on the model. The data indicate that the crystallites may impose slight restrictions on the segmental mobilities in the amorphous regions, but the effect is not pronounced. Some differences between steady and transient state diffusion coefficients are explained in terms of “dead volume” which is present in the steady state of flow to a greater extent than in the transient state.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 315-329 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption and permeation of benzene, acetone, and methanol in and through ethyl cellulose has been investigated from the point of view of hysteresis and time-dependence. The three sorbates are imbibed decreasingly in the order given, at any relative pressure, and so swell the polymer to different extents. The medium is one in which anomalous diffusion is to be expected. The study was made in the lower range of concentrations of penetrant. The initial isotherm of acetone at 50°C. lay below subsequent ones at the same temperature. The higher the temperature the smaller this difference tended to be, while the greater the pressure and so the amount imbibed the greater it became. Eventually “settled” reproducible isotherms were found. If the outgassed polymer, following lower temperature isotherms, was “annealed” at a higher temperature and then cooled again, the initial isotherm at 50°C. was more nearly approached. However, subsequent isotherm determinations at the same temperature again established the “settled” isotherm. Permeation rates were determined as a function of pressure under various treatments. Repeated permeation runs caused the permeability of the polymer to decrease to a “settled” value. This behavior may be ascribed to some orientation of polymer, by mass flow, during permeation. After establishing the settled permeability the polymer was outgassed and “annealed” at a higher temperature, and the permeability at the original temperature then lay below the “settled” value. Benzene, which swelled the membrane more than the other sorbates, showed more pronounced effects of the same kind as acetone. On the other hand methanol, which was least sorbed, showed less pronounced time- and history-dependence. Sorption always occurred more slowly than desorption. The various effects have been discussed in terms of a model of the polymer having rather stiff chains with some semipermanent interchain bonds, but other bonds more easily rearranged. The history-dependent effects can arise at temperatures well above the glass transition usually quoted for ethyl cellulose.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 377-386 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An account has been given of sorption and diffusion of water by ethyl cellulose. In contrast with diffusion coefficients of some other penetrants, those of water decrease with increase of water sorption in the manner previously observed by Rouse for water-polythene systems. The sorption isotherms have the opposite curvature to Langmuir or Freundlich isotherms, and hence also to the isotherms of benzene, C4 and C5 paraffins, or acetone sorbed at low penetrant concentration by the same polymer. The results have been interpreted in terms of cluster formation of water molecules either in preexisting cavities in the polymer or, less probably, in the polymer matrix itself. Visual evidence of cluster formation is provided by the onset of light scattering by the membrane as the relative humidity reaches a critical range. The opacity disappears again as the humidity is decreased.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 23 (1983), S. 653-662 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The shifts in ionization energies which occur when a molecule is incorporated as an asymmetric dimer or in an intermolecular complex are analyzed theoretically. MO—SCF calculations with 4-31G basis sets were performed on closed- and open-shell states of (HF)2, H2O·HF, and their valence-hole ions, as well as on the heterodimers incorporating the higher homologues CH3F, CH3OH, and (CH3)2O. The analysis concerns the influence of electrostatic, polarization, and charge transfer effects associated with complexation on the initial molecular state of each monomer system, as well as monomer-dimer differences in the electronic relaxation mechanism considered as a final state effect in the ionization process. The calculated ionization energy shifts which agree well with the experimental data available for (CH3)2O·HF, show that the shifts are dominated by electrostatic effects, but some effects arising from differences in molecular size and electric polarizability of the monomers can be discerned.
    Additional Material: 3 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1984), S. 583-588 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In recent years stable isotopes have begun to replace radioisotopes as tracers in metabolic studies. However, these are relatively expensive in the enrichments and quantities required by either conventional gas chromatography/mass spectrometry (GC/MS) or stable isotope ratio analysis (SIRA), the former having good sensitivity but low precision and the latter low sensitivity with more than adequate precision. We describe here a technique for 13C which achieves an appropriate balance between precision and sensitivity for such studies. A combustion interface is placed between the output from a capillary gas chromatograph and a dual collector SIRA mass spectrometer. Compounds eluting from the gas chromatograph are converted into discrete pulses of CO2 gas and intensities of 13CO2 and 12CO2 are measured simultaneously. Typically, 13C relative abundances can be obtained from 0.8 nmol of a C10 compound (8 nmol CO2) with a precision (1SD) of better than 1‰ (0.0011 at.%13C). This permits a reduction by at least a factor of 10 in the quantity of tracer required compared with conventional methods.
    Additional Material: 3 Ill.
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  • 8
    ISSN: 0192-253X
    Keywords: Dictyostelium discoideum ; revertants of stmF mutants ; cGMP metabolism ; cGMP-specific phosphodiesterase ; suppressor mutations ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: stmF mutants of Dictyostelium discoideum produce long, banded aggregation streams on growth plates and exhibit altered cGMP metabolism. To learn more about the role of cGMP in chemotaxis and the nature of the defect in these mutants, 15 nonstreaming (Stm+) revertants of two stmF mutants were isolated and characterized. Fourteen of the revertants continued to show the elevated cAMP-induced cGMP response and very low cGMP-specific phosphodiesterase (cGPD) activity characteristic of their stmF parents. Parasexual genetic analysis revealed that many of these Stm+ revertants carried phenotypic suppressors unlinked to stmF. One Stm+ revertant, strain HC344, exhibited a low, prolonged cGMP response and relatively high cGPD activity throughout development. To determine whether the elevated cGPD activity in this revertant resulted from increased enzyme production or enhanced enzyme activity, cGPDs were partially purified from the wild-type strain, the stmF parent and revertant HC344, and properties of the enzymes were compared. cGPDs from the stmF mutant and the revertant showed similar differences from the wild-type enzyme in kinetic properties, thermal stability, and sensitivity to certain inhibitors. These results suggest that stmF is the structural gene of the cGPD. In addition, the unusual cGMP response in revertant HC344 appeared to be due to increased production of an altered cGPD.
    Additional Material: 5 Ill.
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  • 9
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deuterium labelled analogues of the major zeatin derived cytokinins have been synthesized to serve as internal standards for mass spectrometric quantitation. A procedure for the isolation, high performance liquid chromatographic purification and direct probe mass spectrometric analysis of these cytokinins has been devised and applied to the analysis of Zea mays kernels where the levels of endogenous zeatin, zeatin-9β-riboside and zeatin-9β-glucoside were estimated by isotope dilution. Additionally, the deuterated compounds have been utilized to confirm the identity of the in vitro enzymic glucosylation products of zeatin.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 3 (1982), S. 283-297 
    ISSN: 0192-253X
    Keywords: Dictyostelium discoideum ; cAMP-unresponsive mutants ; parasexual genetic analysis ; cell differentiation ; chemotaxis to folate and cAMP ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: To find mutants of Dictyostelium discoideum that are unable to respond to exogenous cAMP signals (frigid mutants), amoebae of 218 independent aggregation-deficient mutants were treated in suspension with artificial pulses of cAMP and screened for the capacity to form EDTA-resistant cohesion sites. Eleven frigid mutants were identified and further characterized. Using parasexual genetic techniques, these strains were assigned to five complementation groups (fgdA-E) and the fgd loci were mapped in three linkage groups: fgdA and D in group II, fgdC in group III, and fgdB and E in group VII. Biochemical and physiological experiments with these strains indicated that fgd mutants are of two general types. When starved, strains in groups fgdB, D, and E failed to produce detectable levels of membrane-associated cAMP phosphodiesterase, surface cAMP receptors, or extracellular phosphodiesterase inhibitor, and the cells continued to respond chemotactically to folate. Thus, these strains are probably arrested in the vegetative phase or very early in development. In contrast, strains in groups fgdA and C produced low levels of cAMP receptors and secreted phosphodiesterase inhibitor. Moreover, after starvation, some of these mutants elicited a weak chemotactic response to cAMP. Therefore, unlike the former group of mutants, these strains appear to initiate development when starved, but the process is blocked at an early stage.
    Additional Material: 1 Ill.
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