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  • Chemistry  (24)
  • 2010-2014
  • 2000-2004
  • 1995-1999  (15)
  • 1960-1964  (9)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 53 (1997), S. 332-338 
    ISSN: 0006-3592
    Keywords: α-hydroxynitrile lyase ; cassava ; cyanogenesis ; cyanohydrin ; Escherichia coli expression vector ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The coding sequence of the cyanogenic α-hydroxynitrile lyase gene of Manihot esculenta Crantz (cassava) was cloned in the plasmid vector pMal-c2 and expressed in Escherichia coli strain JM105. DNA sequencing showed that the recombinant plasmid contained the same sequence as the cDNA clone pHNL10. Peptide sequencing of the recombinant protein showed that the N-terminus was heterogeneous, with either four or six additional amino acid residues compared with the native protein. Circular dichroism spectra indicated similar secondary structure contents for both proteins. Enzyme assays showed that specific activity of native and recombinant proteins were 0.24 and 0.26 mmol CN-/mg/min, respectively; that both proteins had optimal activity at 40°C and pH 5.5; and that both proteins were inhibited by the serine protease inhibitor phenyl-methane sulfonyl flouride (PMSF). Isoelectric focusing of native and recombinant protein revealed multiple isoforms for both proteins; the recombinant protein had a more basic mean isoelectric point (pl) (5.1) than the native protein (4.5). © 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 53: 332-338, 1997.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 18 (1995), S. 54-58 
    ISSN: 0935-6304
    Keywords: High resolution capillary GC ; High resolution GC-MS ; Zeolite ZSM-5 ; Copaiba tree (Copaifera officinalis) ; Copaiba oil ; Fuel oil ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oil extracted from the trunk of the copaiba tree (Copaifera officinalis) is composed of sesquiterpenes, C15H24, and a small amount (〉7 %) of sesquiterpenols, C15H26O; these were identified from their Kováts indices and mass spectra. The use of zeolites in the catalytic transformation of this renewable source of hydrocarbons is of interest in the search for new chemicals and ecologically clean fuels. Oil samples from copaiba trees growing in Colombia's Oriental Plains were circulated over zeolite ZSM-5 in a continuous flow fixed-bed micro reactor at 225, 265, and 325°C, for 1 h and subsequently analyzed by HRGC and GC-MS. Whereas only thirty four sesquiterpenes were identified in the original oil, over two hundred compounds were found in the product of the treatment of copaiba oil with zeolite ZSM-5. This complex mixture of sesquiterpenes, light aromatic compounds, and indene and naphthalene derivatives resulted from reactions such as isomerization, hydrogenation, cracking, and dehydrogenation with and without cracking. The amount of cracking products and aromatic compounds increased with reactor temperature but decreased with catalyst aging.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 51 (1996), S. 112-119 
    ISSN: 0006-3592
    Keywords: biodegradation ; self-cycling fermentation ; phenol ; Pseudomonas putida ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Self-cycling fermentation (SCF) in a stirred tank reactor was applied to the biodegradation of phenol by Pseudomonas putida. The technique resulted in stable and repeatable performance. Complete substrate consumption was achieved under all operating conditions investigated. SCF resulted in substrate utilization rates as high as 14.5 kg of phenol per cubic meter of fermentor volume per day of fermentation, higher than those that have been reported for batch, CSTR, and packed column fermentors. A mathematical model of the self-cycling fermentation process was expanded to include inhibitory substrate-microorganism combinations, and was shown to provide a good fit to both end-of-cycle and intracycle experimental data. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 6 (1964), S. 247-270 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The effects of ambient pressure and ultrasonic power on the disintegration of yeast suspension have been investigated. The results obtained are, in the main, consistent with the theory that cell breakage is primarily a phenomenon dependent on producing gaseous cavitation in the medium. The importance of the experimental results and techniques applied to Commercial cell disintegrators is briefly discussed. A simple flow system is described which is easily attached to probe-type disintegrators. The use of a crystal pickup for tuning and control purposes is described.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 580-588 
    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: Torsional modulus-temperature data have been obtained on heterogeneous polymer compositions prepared by several procedures. Both the state of aggregation of the component chain molecules and their degree of compatibility are significant variables. Modulus curves similar to those for crystalline polymers can be obtained from incompatible polymers having glass temperatures sufficiently far apart. Detailed interpretations are presented for modulus curves of both individual homopolymers and bicomponent heterogeneous polymer mixtures.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 59-69 
    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 isolation of two graft copolymers of styrene on polyethyl acrylate from the ungrafted homopolymers by solvent extraction procedures is discussed. For the grafts and their corresponding mixtures ηsp/c versus c plots were determined, and no anomalies were observed. Qualitative data on the solubilities and phase properties of the grafts are given. Torsional modulus-temperature curves are shown for graft copolymer and the individual homopolymers.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1541-1548 
    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: Differential thermal analysis (DTA) and thermogravimetric analysis (TGA) of poly(ethylene terephthalate) has been carried out on samples of amorphous, cold-drawn, heat-crystallized, and acetone-crystallized polymer. From DTA it appears that for amorphous material a prolonged “secondary” crystallization process follows a primary process in the region of 140°C. For cold-drawn polymer, heat treatment does not reflect differences observed in previous x-ray diffraction studies. The TGA gives evidence that a high temperature endothermic peak observed in DTA may not be directly associated with depolymerization. With acetone-crystallized material a high degree of acetone retention is detected.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 337-348 
    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 predicted general incompatibility of mixtures of polymers has been further confirmed. Thirty-one mixtures of homopolymer pairs showed phase separation in a common solvent. These included closely related polymers such as polyacrylates with both polymethacrylates and other polyacrylates and pairs of different polymethacrylates. Typical immiscible combinations are PMA/PEA and PEMA and PEMA/PMMA. It was also found that the presence of a common monomer constituent did not result in complete compatibility of either a homopolymer with a copolymer or a mixture of two copolymers. Apparently, none of the combinations tried were sufficiently similar to result in heats of interaction small enough to be counteracted by the small entropy change involved. Since another possibility for attaining miscibility is through polar interactions, the effects of ionic and hydrogen-bonding substituents upon polymer-polymer compatibility were considered, and selected experiments were done on a series of carboxyl-containing polymers and their sodium salts. It was concluded that hydrogen bridging occurs preferentially either intramolecularly or between polymer and solvent rather than between two different types of chains each having hydrogen-bonding ability. Thus, poly(acrylic acid) and poly(methacrylic acid) show two-phase separation in water. Although poly(sodium acrylate) and poly(sodium methacrylate) are completely miscible, mixtures of the partially neutralized acids, e.g., PAA and PNaMA mixtures, show separation. In contrast to predictions for less polar polymers, compatibility of mixtures of polymers containing high mole fractions of carboxylic acid monomers showed a pronounced dependence upon solvent. Thus, the two copolymers 45/53 EA-MAA and 47/53 MMA-MAA are incompatible in methanol or ethanol but form homogeneous solutions in DMF or DMS.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The behavior of polymer - solvent systems has been studied as a function of hydrostatic pressure to 3000 atm. The swelling of crosslinked neoprene and crosslinked Hevea has been studied in several solvents, and the temperature of phase separation of polystyrene in cyclohexane has been determined. These measurements permit an indirect evaluation of the volume of mixing that is felt to have advantages over the direct method due to the small magnitude of the effect in polymer systems. In all of the cases studied by the swelling technique, the volume of mixing is negative and tends to be greater in magnitude the better the solvent. For the very poor solvent - polymer system studied by the precipitation technique, a small positive value is obtained. In addition, the compressibility of swollen polymers is compared with that expected from an assumption of additivity and found to be much smaller. These phenomena are presumably the result of a more tightly packed liquid structure within the polymer network. This explanation suggests that the descriptions of the volume of mixing in terms of the apparent specific volume, while certainly formally correct, may be misleading physically. An attempt to relate the observations on these systems to a theory involving a power series expansion in terms of the solvent fugacity was unsuccessful due to the slow convergence of the series.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 61 (1962), S. S28 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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