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  • Chemistry  (743)
  • Cell & Developmental Biology  (49)
  • Humans
  • Wiley-Blackwell  (792)
  • 2020-2022
  • 1980-1984  (486)
  • 1970-1974  (306)
  • 1980  (486)
  • 1970  (306)
  • 1
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Gram-sized quantities of purified arginine, formylmethionine, glutamic acid, and phenylalanine-2 tRNAs have been prepared from pools of E. coli K-12 MO7 mixed tRNAs by reversed-phase chromatography after preliminary fractionation on DEAE-cellulose. Purified formylmethionine tRNA and partially purified arginine tRNA and glutamie acid tRNA were obtained from large-scale RPC-3 runs (4 × 36 in. column). The arginine tRNA was further purified by rechromatography on RPC-4 columns, and the gluatmic acid tRNA by rechromatography on an RPC-3 column. Two phenylalanine tRNAs were resolved on large-scale (2 × 96 in. column) RPC-3 runs; only the second phenylalanine tRNA reached a satisfactory degree of activity. About 0.88 g of arginine tRNA, 70% activity; 3.32 g of formylmethionine tRNA, 97% activity; 0.80 g of glutamic acid tRNA, 83% activity and O.92 g of phenylalanine-2 tRNA, 78% activity, were produced. The processing steps employed are reliable and reproducible and the procedure is amenable to routine production of these tRNAs.
    Additional Material: 9 Ill.
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  • 2
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As part of a study to make a comparative analysis of selected halogenated compounds in man and the environmental media, a quantitative gas chromatographic mass spectrometric analysis of the levels of the halogenated compounds found in the breath, blood and urine of an exposed population (Old Love Canal area, Niagara, New York) and their immediate environment (air and water) was undertaken. In addition, levels of halogenated hydrocarbons in air samples taken in the general Buffalo, Niagara Falls area were determined.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 4 (1970), S. 145-187 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The influences of the conditioning treatments, surface topography, and crystal structure of carbonaceous surfaces on their ability to sorb heparin and their in vivo compatibility with blood were investigated. The results of the sorption studies indicated that the adsorption of heparin on the surfaces of turbostratic and graphitic materials is not crystallographically selective and that the amount adsorbed on relatively smooth surfaces is near the amount expected for monolayer formation. Although the adsorption of heparin on relatively smooth carbon surfaces is not influenced by the presence of benzalkonium chloride, the sorption of heparin in porous carbons can be greatly increased by a pretreatment with benzalkonium chloride. This increase was found to be due to the formation and entrapment of the insoluble heparin-benzalkonium complex in the accessible porosity. Since the heparin sorptions in Dag-154 coatings were found to be enhanced by a pretreatment with benzalkonium chloride, it was inferred that these coatings contain accessible porosity and that their initial thromboresistance depends on the formation of the benzalkonium-heparin complex in pores. In vivo tests showed that polished and outgassed, impermeable isotropic carbons deposited at low temperatures were significantly thromboresistant without the exogenous application of heparin. There was no relationship between the amount of heparin sorbed on these materials and their compatibility with blood. Polishing, for example, which reduced heparin sorption, enhanced the thromboresistance of these carbons, and while chemisorption of oxygen markedly reduced their thromboresistance, it did not influence the amount of heparin that could be sorbed. Although the heparin-benzalkonium complex sorbed in a porous carbon conferred excellent thromoboresistance in a 2-hr test, the long-tern (14-day) compatibility was not as good as for carbon surfaces that were deposited at low temperatures and then polished and outgassed prior to implanting. In vivo tests of HTI carbon structures and annealed LTI carbons indicate that the blood compatibility of a turbostratic carbon is not significantly dependent on crystallite size, Le. Limited tests of surfaces that had a preponderance of c-faces oriented parallel to the blood-carbon interface at the surface suggest that orientations of this sort are better than others.
    Additional Material: 15 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 2 (1980), S. 5-10 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Mean free paths for inelastic scattering (λ) of low energy electrons in poly(methylmethacrylate) (PMMA) have been determined by measuring Al Kα excited C 1s and Si 2s photoelectron signal intensities as a function of ellipsometrically determined thicknesses of PMMA overlayers on silicon substrates. The λ values obtained are 29 ± 4 Å for 1196 eV electrons and 33 ± 5 Å for 1328 eV electrons. These data are necessary for the quantitative analysis of the surface region of PMMA and similar polymers by X-ray photoelectron spectroscopy (XPS). The magnitude of the λ values determined indicates that XPS measurements can provide chemical information about the surface region of polymers, such as PMMA, in the depth range of ∼6 to 100 Å. The results of this study are compared and discussed with respect to λ values determined for other organic compounds.
    Additional Material: 7 Ill.
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  • 5
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: In the poor solvent acetone/ethanol the viscosity of a 3% solution of 12.6% N pyro nitrocellulose is found to be related to the geometric mean of the number average and weight average molecular weights. The fractional increase in the viscosity of such a solution on the addition of lead ß-resorcylate is a function only of number average molecular weight. Once calibration has been made against osmotic pressure measurements and intrinsic viscosity, both number and weight average may be measured rapidly with an accuracy which is no less than that of the osmotic pressure and intrinsic viscosity measurements themselves.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 9 (1980), S. 230-238 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The IR spectra (1400 cm-1 to 160 cm-1) of the gases at ambient temperature and the Raman spectra (below 1400 cm-1) of the liquids near -196°C are reported for CF3OF and CF3OCl. All fundamentals are assigned under Cs symmetry and the results of a normal coordinate analysis are presented. The assignments of Smardzewski and Fox are adopted with one exception for both CF3OF and CF3OCl: the CF3 rock of A″ symmetry is assigned near 430 cm-1 and the two bands between 200 cm-1 and 300 cm-1 are assigned to an A′ fundamental, involving CF3 rocking and COX bending and a Δν=2 transition in the CF3 torsion. An extra band at 548 cm-1 in the Raman spectrum of liquid CF3 COl near -196°C is assigned to a CF3OCl⃛Cl2 complex. The values of the force constants d(OX) for CF3OX molecules are suggested to be near those for X2O molecules. More than half the normal modes of A′ symmetry show extensive mixing of symmetry coordinates. In some of these cases the symmetry coordinate for which the normal mode is named is the largest but not the dominant contributor to the potential energy distribution, while in others this symmetry coordinate is not even the largest contributor to the potential energy distribution. No normal modes of A′ symmetry are present in which ν(CO), δs(CF3), δ(COX), or δ(CF3) symmetry coordinates are dominant, and the mode conventionally labeled as v(CO) should be labeled as νs(CF3). For the remaining A′ normal modes and all the A″ normal modes, the symmetry coordinate for which the normal mode is named is dominant in the potential energy distribution.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of poly(ε-L-lysine) is described. This is a poly(ε-amino acid) in which the ε-amino group of lysine is condensed with the α-carboxyl group to produce a chain backbone that is a variant of the usual one seen in proteins and the side chain is the α-amino group. Conformational studies of poly(ε-L-lysine) and its t-butyloxycarbonyl derivative suggest the likelihood of a chain order that is formally similar to the antiparallel pleated-sheet conformation of proteins.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1841-1846 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photo-oxidation of solid polymers at ambient temperatures is shown to be greatly affected by the low mobility of radicals in the solid state. When a radical pair, produced by photo-initiation, escapes the initial polymer cage, the probability of its recombination remains high even after several propagation steps. This phenomenon, known as secondary cage recombination, has a pronounced effect on the kinetics of oxidation and on the mechanism of photostabilisation by radical scavengers. The occurrence of secondary cage recombination is demonstrated for polypropylene photo-oxidation and a kinetic analysis is developed to predict the consequences of this effect.
    Additional Material: 2 Ill.
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  • 9
    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 thermal degradation of a bisphenol A-based epoxy resin (EP 274) cured with 4,4′-diaminodiphenyl methane (DDM) and with phthalic anhydride (PA) was studied using a radiochemical pyrolysis gas chromatography technique. Conclusive evidence for some of the degradation mechanisms of these resins was obtained by pyrolyzing samples containing various 14C-labelled groups and analyzing the products using this method.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 611-632 
    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: A stress relaxation technique was used to study the kinetics of the photo-oxidation of plasticized poly(vinyl chloride) film. The effects of ultraviolet irradiation were characterized by the slope of a difference line between the stress relaxation curve of an irradiated test sample and that of a nonirradiated control. An activation energy of 12 kcal/-mole was obtained for the rate-controlling reaction, which was postulated to be hydrogen abstraction from the substrate by peroxy radicals. The rate of relaxation was dependent on the radiation energy, being greater at lower energies. It was also independent of oxygen pressure at “high” pressures and dependent at “low” pressure. The nature of the plasticizer and the presence of stabilizer and ultraviolet absorbers all affected the relaxation behavior.
    Additional Material: 8 Ill.
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