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  • General Chemistry  (10)
  • Polymer and Materials Science  (7)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 344-345 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 80 (1968), S. 118-119 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 890-890 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrachlorkohlenstoff läßt sich aus Phosgen bei 300 bis 450°C darstellen, wenn man die Reaktion durch Übergangsmetalle der V. bis VIII. Gruppe des Periodensystems auf Aktivkohle katalysiert. Statt Phosgen sind auch Kohlenmonoxyd und Chlor als Ausgangsstoffe brauchbar.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 1607-1612 
    ISSN: 0887-6266
    Keywords: neutron scattering (SANS) from hot stretched polystyrene ; polystyrene, hot stretched, SANS study of ; chain deformation in hot stretched polystyrene, SANS study of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle neutron scattering (SANS) has been used to investigate macromolecular orientation of uniaxially hot-stretched partially deuterated polystyrene. Principle radii of gyration and degree of eccentricity were measured over a range of hot-stretch temperatures, strain rates, and external draw ratios (EDR). Results show affine deformation for EDR 〈4 and an increase in the degree of local molecular orientation with increasing rate of strain and decreasing stretching temperature. It also is found that although the macromolecules follow the external stretching affinely on average, they do not deform uniformly.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 60 (1988), S. 152-153 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 39 (1998), S. 539-548 
    ISSN: 0021-9304
    Keywords: cytokine delivery via covalent binding ; tissue repair ; biomaterials ; collagen ; transforming growth factor β ; polyethylene glycol ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: To overcome rapid diffusion and clearance from the implant site and to increase stability, recombinant transforming growth factor β2 (TGF-β2) was covalently bound to injectable bovine dermal fibrillar collagen (FC) and its activity compared to admixed TGF-β2. Covalent binding was achieved in a two-step procedure: First, TGF-β2 was reacted with the difunctional polyethylene glycol (PEG) linker, and then the PEG-attached TGF-β2 (PEG-TGF-β2) was bound to the fibrillar collagen (FC-PEG-TGF-β2). Initial binding of TGF-β2 to difunctional succinimidyl glutarate (D-SG-PEG) or succinimidyl propionate polyethylene glycol (D-SE-PEG) linkers was completed after reacting for 8 or 10 min as monitored by reverse-phase high-performance liquid chromatography. After reaction with injectable fibrillar collagen, extraction of unbound PEG-TGF-β2 and Western blot analysis, using a TGF-β specific antibody, demonstrated that at least 85% of the TGF-β2 was bound to the fibrillar collagen. The activity of PEG-TGF-β2 was fully stable in phosphate-buffered saline at 4°C and 37°C for at least up to 4 weeks. Unmodified TGF-β2 mixed with fibrillar collagen was completely inactivated after 1 week of incubation, as measured by the mink lung epithelial cell (Mv1Lu) growth inhibition assay. Formulations of FC-PEG-TGF-β2 containing 40 μg/mL TGF-β2 were implanted subcutaneously into rats and analyzed after days 7, 21, and 42. All TGF-β2-containing formulations showed the TGF-β typical fibroblastic response at the day 7 time point. Covalent binding of TGF-β2 to collagen with both difunctional PEG crosslinkers resulted in a significantly stronger and longer-lasting TGF-β2 response than that observed with admixed formulations of collagen and TGF-β. The TGF-β response with FC-PEG-TGF-β2 lasted up to day 42 but was not seen after day 7 for TGF-β2 admixed to FC. These findings clearly demonstrate that TGF-β2 remains fully active after being covalently bound to collagen via difunctional PEG. In addition, covalent binding potentiates and prolongs in vivo TGF-β responses and stabilizes the TGF-β in vitro. Results suggest that this method of formulation could be useful to stabilize and deliver similar peptide growth factors or biologically active agents. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 39, 539-548, 1998.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 47 (1960), S. 417-433 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phosphorus trichloride and oxygen react readily with polyethylene to introduce phosphonic dichloride ( - POCl2) groups into the polymer (chlorophosphonation). Treatment of the resulting intermediate with water, alcohols, and amines yields polymeric alkylphosphonic acids, esters and amides, respectively. Derivatives containing as much as 16% phosphorus have been prepared. With increasing degree of phosphonation, polyethylene crystallinity is reduced, the acid and amide derivatives become stiffer, less extensible, and less soluble in nonpolar solvents, and internal plasticization is observed in the ester derivatives. No significant decrease in flammability is effected by phosphonation unless chlorine is introduced also. The ester and amide derivatives crosslink under mild conditions by an unknown mechanism, the acid derivative will crosslink on heating with litharge. The chlorophosphonation reaction is sensitive to inhibitors and no highly active catalyst was found. The rate appears to be governed by the rate at which oxygen dissolves in the mixture. Substitution of air or chlorine for oxygen, phenyldichlorophosphine or diphenylchlorophosphine for phosphorus trichloride results in introduction of phosphorus-containing groups into polyethylene, also, but at reduced rates. In sharp contrast to polyethylene's apparent stability toward the phosphonation conditions, polystyrene, poly(methyl methacrylate), and polyisobutylene undergo a rapid decrease in molecular weight on treatment with phosphorus trichloride and oxygen. The fact that these four polymers exhibit the same relative behavior, i.e., polyethylene is stable whereas the other three polymers are unstable, in various free radical processes argues for a free radical mechanism in the chlorophosphonation reaction.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 46 (1960), S. 547-550 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0570-0833
    Keywords: Carbon tetrachloride ; Phosgene ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon tetrachloride can be prepared from phosgene at 300-450°C. The catalysts for the reaction are transition metals of Groups V to VIII deposited on activated charcoal as carrier. Carbon monoxide and chlorine may be used as starting materials instead of phosgene.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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