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  • Articles  (29)
  • Wiley-Blackwell  (18)
  • Springer  (11)
  • Cambridge University Press
  • Mineralogical Society of America
  • Mineralogical Society of Great Britain and Ireland
  • Public Library of Science (PLoS)
  • Chemistry and Pharmacology  (29)
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  • Articles  (29)
  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Nanosize poly(methyl methacrylate) (PMMA) microlatexes with high PMMA/surfactant ratio have been successfully prepared by a modified microemulsion polymerization, i.e., continuous and slow addition of monomer (MMA) to the polymerizing MMA microemulsion with mild stirring. Number-average diameters of 33–46 nm with narrow polydispersity (Dv/Dn= 1.1) and polymer content of 6–24 wt% were achieved using low levels of surfactant (dodecyltrimethylammonium bromide, DTAB) — less than 1 wt% of the reaction mixture. Particle diameter depended on polymerization temperature, MMA content, and concentrations of initiator and surfactant. Larger particles wereformed when temperature was too high, initiator concentration was too high, or surfactant concentration was too low.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4919
    Keywords: creatine kinase ; mitochondria ; respiration ; contraction ; regulation ; thermodynamics ; compartmentation ; functional coupling ; metabolic channelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Some historical aspects of development of the concepts of functional coupling, metabolic channelling, compartmentation and energy transfer networks are reviewed. Different quantitative approaches, including kinetic and mathematical modeling of energy metabolism, intracellular energy transfer and metabolic regulation of energy production and fluxes in the cells in vivo are analyzed. As an example of the system with metabolic channelling, thermodynamic aspects of the functioning the mitochondrial creatine kinase functionally coupled to the oxidative phosphorylation are considered. The internal thermodynamics of the mitochondrial creatine kinase reaction is similar to that for other isoenzymes of creatine kinase, and the oxidative phosphorylation process specifically influences steps of association and dissociation of MgATP with the enzyme due to channelling of ATP from adenine nucleotide translocase. A new paradigm of muscle bioenergetics - the paradigm of energy transfer and feedback signaling networks based on analysis of compartmentation phenomena and structural and functional interactions in the cell is described. Analysis of the results of mathematical modeling of the compartmentalized energy transfer leads to conclusion that both calcium and ADP, which concentration changes synchronously in contraction cycle, may simultaneously activate oxidative phosphorylation in the muscle cells in vivo. The importance of the phosphocreatine circuit among other pathways of intracellular energy transfer network is discussed on the basis of the recent data published in the literature, with some experimental demonstration. The results of studies of perfused rat hearts with completely inhibited creatine kinase show significantly decreased work capacity and respectively, energy fluxes, in these hearts in spite of significant activation of adenylate kinase system (Dzeja et al. this volume). These results, combined with those of mathematical analysis of the energy metabolism of hearts of transgenic mice with switched off creatine kinase isoenzymes confirm the importance of phosphocreatine pathway for energy transfer for cell function and energetics in mature heart and many other types of cells, as one of major parts of intracellular energy transfer network and metabolic regulation.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 18 (1930), S. 751-752 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 256 (1978), S. 96-96 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 5
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 141-163 
    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 previously reported synthetic procedure was used to graft oligo-p-hydroxybenzoic acid (oligo-PHBA) to COOH-functional acrylic copolymers. Most of the products were side-chain LC copolymers. Length of the mesogenic oligo-PHBA groups averaged up to five aromatic rings per group. Because these long mesogenic groups have a strong tendency to form LC domains, it was possible to prepare LC side-chain copolymers having as little as 5 mol % of mesogenic monomer. Thus this synthetic procedure provides a versatile route for exploration of the properties of LC copolymers having relatively few but especially effective mesogenic groups. The potential utility of such LC copolymers as binders for nonbake coatings was assessed. Variables studied were molecular weight and Tg of the acrylic copolymer backbone, number and average length of oligo-PHBA segments, and the presence or absence of a flexible spacer between the acrylic backbone and the PHBA segments. Optimum LC copolymers have moderate (15,000-30,000) Mn, low (-10°C) backbone Tg, and low (5-7.5 mol %) population of long (5 PHBA units) oligo-PHBA units. Such copolymers have two major advantages as coatings binders: They form concentrated, stable, low-viscosity dispersions in common solvents, a very desirable characteristic for application. Coating films have excellent adhesion to metal, and they have an extraordinary combination of hardness (H-2H) and impact resistance (〉 80 in. Ib). These properties are key indicators of coating performance and indicate that LC copolymers have excellent potential for use as binders for nonbake coatings. Other properties remain to be investigated.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1109-1125 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for grafting oligo-(p-hydroxybenzoic acid) to carboxyl-functional oligomers or polymers to give copolymers having mesogenic side chains was developed. The method employs dicyclohexylcarbodiimide (DCC) to promote esterification of PHB at mild temperatures and to remove water. Pyridine is used as solvent, and catalytic amounts of p-TSA are added to suppress side reactions. Grafting efficiencies are estimated to range from 74 to 90%. Ungrafted oligo-PHB and other by-products are readily removed. Structure assignments were supported by IR,1H-NMR, GPC, DSC and model compound studies. The method appears capable of grafting oligo-PHB side chains to any pyridine soluble oligomer or polymer having carboxyl groups and no other reactive groups that could interfere.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1075-1079 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymer nanoparticles were prepared from monomers such as styrene (St), butyl methacrylate (BMA), butyl acrylate (BA), methyl methacrylate (MMA), and methyl acrylate (MA) using a modified microemulsion polymerization process. With this process high polymer: surfactant weight ratios (7 : 1 or greater), relatively concentrated (10-30 wt.-%) latexes and small (10-20 nm) particle diameters were attained. Nucleation mechanisms were investigated through observations of the particle size change during the polymerization.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2517-2520 
    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
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1903-1909 
    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 commercial hexakis(methoxymethyl)melamine (HMMM) resin was fractionated (1) by crystallization of the hexane-soluble fraction from hexane and (2) by partitioning the hexane-soluble and hexane-Insoluble fractions between alumina and various solvents. Crystallization afforded hexakis(methoxymethyl)melamine (1) of 90 to 95% purity. Partitioning afforded 12 fractions with altered proportions of polar and nonpolar species; the least polar fraction was spectroscopically and chromatographically similar to the crystallized material. Relative reactivities of certain fractions were estimated by 1H NMR studies of the rates of reaction with neopentyl alcohol in the presence of catalytic amounts of p-toluenesulfonic acid (p-TSA). It was found that the reactivity of fractions, rich in less-polar species, was substantially greater than that of the commercial HMMM resin, whereas reactivity of fractions, rich in polar species, was less. Reactivity was especially enhanced by removal of all active hydrogen species, notably those containing NH groups. A practical consequence of this result was that fully formylated and alkylated melamine resins could crosslink with polyols at substantially lower temperatures than the commercial HMMM resin, which contained NH groups. Therefore, room-temperature crosslinking was feasible.
    Additional Material: 1 Ill.
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