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  • 1
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    Biofuels and Sustainability : Holistic Perspectives for Policy-making (2018)
    Tokyo : Springer
    Details
    Keywords: Environment ; Renewable energy resources ; Energy policy ; Energy and state ; Ecosystems ; Renewable energy sources ; Alternate energy sources ; Green energy industries ; Environmental law ; Environmental policy ; Environmental management ; Sustainable development ; Environment ; Sustainable Development ; Energy Policy, Economics and Management ; Ecosystems ; Environmental Management ; Renewable and Green Energy ; Environmental Law/Policy/Ecojustice
    Description / Table of Contents: Preface.-Introduction.-Part 1: Biofuels and Sustainability Conceptual Framework --- Chapter 1. Sustainability Science Perspective for Biofuels [Takeuchi, Matsuda] --- Chapter 2. Stakeholder perspectives and Multilevel Governance [Shiroyama, Matsuura] --- Chapter 3. Applying stakeholder perspectives to sustainable biofuel strategy: a summary of our analyses [Shiroyama, Matsuura].-Part 2: Impacts on land use and ecosystem services --- Chapter 4. Global Economic and Environmental Impacts - Economic Impacts of biofuels and related policy [Suzuki and Takahashi] --- Chapter 5. Global Economic and Environmental Impacts - Environmental impacts of biofuel production on the GHG emission reduction [Hanaki] --- Chapter 6. Impacts at the National & Regional Scales - Land use change impacts [Hayashi] --- Chapter 7. Impacts at the National & Regional Scales - Socioeconomic impacts in East Asia [Elder, Kozima, Sano and Hayashi] --- Chapter 8. Social, Economic and Political Impacts - Socio-Political impacts to the roles of stakeholders [Shiroyama and Matsuura ] --- Chapter 9. Social, Economic and Political Impacts - Impacts on ecosystem services [Alexandros and Stromberg] --- Part 3: Sustainable biofuels strategy options --- Chapter 10. Roadmap for building sustainable strategy options - Developing sustainable strategy options [Shiroyama and Matsuura] --- Chapter 11. Roadmap for building sustainable strategy options - Application of Ontology for developing strategy options [Kozaki, Mizoguchi and Saito] --- Chapter 12. Key strategies for policy makers - Global Strategies options [Arai, Matsuda and Suzuki] --- Chapter 13. Key strategies for policy makers - Regional Strategy options for East Asia [Elder, Kozima, Sano and Hayashi] --- Chapter 14. Key strategies for policy makers - National strategy options for Japan [Shiroyama, Matsuura and Saito]
    Pages: Online-Ressource (VI, 265 pages) , 72 illustrations, 22 illustrations in color
    ISBN: 9784431548959
    URL: https://link.springer.com/openurl?genre=book&isbn=978-4-431-54895-9
    Language: English
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    E-BOOK
  • 2
    Electronic Resource
    Electronic Resource
    Alternation-regulating activities of metal halides in the copolymerization of methyl methacrylate and styrene (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 901-904 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170230322
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  • 3
    Electronic Resource
    Electronic Resource
    Polymerization of coordinated monomers. XVII. Alternating copolymerization of methyl methacrylate with styrene by boron compounds (1981)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2581-2594 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By the use of various boron compounds methyl methacrylate and styrene were copolymerized under photoirradiations at -20°C. The alternately regulating activities of the boron compounds in the copolymerizations were in the following order: boron trichloride 〉 ethylboron dichloride 〉 boron trifluoride 〉 diethylboron chloride ≫ triethylboron (≃0). Boron trichloride and ethylboron dichloride exhibited such high regulating activities that their presence in 1 mol% in the charged methyl methacrylate was sufficient to complete equimolar alternating copolymerization. The alternating copolymerization proceeded in the steady state. The copolymerization rates decreased in the following order: boron trichloride ≫ ethylboron dichloride 〉 diethylboron chloride ≫ triethylboron (≃0). The cotacticities of methyl methacrylate-centered triads in the resulting copolymers were identical to those prepared with boron trichloride, ethylboron dichloride, and diethylboron chloride. The mechanism of the alternating copolymerization is discussed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1981.170191018
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  • 4
    Electronic Resource
    Electronic Resource
    Polymerization of coordinated monomers. XV. 13C-NMR study on the alternating copolymers of methyl methacrylate with styrene (1979)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1339-1352 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By the use of various metal halides methyl methacrylate and styrene were copolymerized to produce equimolar alternating sequences and different cotacticities. The 13C-NMR spectra of these copolymers were simple in comparison to those of random copolymers because of the fixed monomer sequence which yielded sharply split triplets for carbonyl, methoxy, and quaternary carbons. The relative intensities in these split peaks varied according to the metal halide used. A comparison of the intensities made it possible to obtain clear-cut and quantitative information on the methyl methacrylate-centered triad cotacticity of the copolymers. The spectral assignment with respect to the methoxy carbon was definitely justified by the combined use of partly relaxed Fourier transform and selective decoupling techniques. The spectrum of aromatic C1 carbon in styrene units also split into three main peaks. From their relative intensities the splitting was attributed to styrene-centered triad cotacticity. The assignment of this carbon was compared with two other assignments made for random copolymers of methyl methacrylate with styrene; they were contradictory, however. Furthermore, an apparent discrepancy was observed between methyl methacrylate-and styrene-centered tactic triads of these alternating copolymers. The origin of this discrepancy suggests a close relationship with the copolymerization mechanism.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1979.170170509
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  • 5
    Electronic Resource
    Electronic Resource
    Polymerization of coordinated monomers. XIX. Kinetic study of the alternating copolymerization of methyl methacrylate with styrene by boron trichloride (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 159-172 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating copolymerizations of methyl methacrylate with styrene in the presence of boron trichloride at 0°C in 1,2-dichloroethane were carried out by using benzoyl peroxide as an initiator. Conversion increased proportionally with polymerization time, whereas the degree of polymerization was constant irrespective of time. The rate depended linearly on the square root of the concentration of benzoyl peroxide. The equilibrium constants for the formation of the ternary molecular complex composed of methyl methacrylate, styrene, and boron trichloride in 1,2-dichloroethane at -20, -10, and +4°C were determined by 1H-NMR spectroscopy. The concentrations of the ternary molecular complex in the polymerization mixtures were evaluated from the equilibrium constant of the formation. The rate of the alternating copolymerization was proportional to the first order of the concentration of the ternary molecular complex. The distribution of methyl methacrylate-centered triads in the alternating copolymer was different from that of styrene-centered triads. These results can be explained by a mechanism involving the homopolymerization of a ternary molecular complex.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170200117
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