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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 45-49 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8900
    Keywords: Carboxylic acid ; biopolyesters ; daltons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The carboxylic acids derived from olive oil, hazelnut oil, sesame oil and hamci(anchovy) oil were evaluated as substrates for cell growth and the production of reserve polyesters by Pseudomonas oleovorans. Poly-3-hydroxy alkanoates containing both saturated(mainly 3-hydroxy-octanoate and 3-hydroxy-decanoate) and unsaturated repeating units with 8 to 20 carbon atoms, or more, were produced in 26 to 61% yields based on cell dry weights. The number average molecular weights of these polymers varied from 45,000 to 68,000 Daltons.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3349-3354 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new polymeric initiator, oligo(adipoyl-5-peroxy-2,5-dimethyl n-hexyl peroxide), was synthesized by interfacial condensation of adipoyl chloride with 2,5-dimethyl-2,5-dihydroperoxy hexane. This can be used as an initiator to prepare block copolymers by free radical mechanism in a procedure involving several steps, since the colorless, viscous liquid, oligoperoxide, has 8-10 peroxide groups per molecule. The thermal decomposition of this oligoperoxide in benzene solution at 98°C was first order and its half life was 9.75 h. The results of the polymerization kinetics show that this oligoperoxide lies in between of 2,5-dimethyl-2,5-dihydroperoxyhexane and benzoyl peroxide for empirical polymerization rates of styrene and methyl methacrylate at 80°C.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1739-1746 
    ISSN: 0887-624X
    Keywords: macromerinitiator (macroinimer) ; crosslinked block copolymer ; macroinitiator ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several new macroinitiators and macromerinitiators (macroinimers) were synthesized and evaluated for the bulk polymerization of sytrene at 60°C. Macroinitiators were prepared from the reaction of 4,4′-dicyano-4,4′ azovaleryl chloride (1) with poly(ethylene glycol) (PEG) with a Mω of 400 and with either benzoyl chloride, acetyl chloride, phenyl isocyanate, or poly(ethylene glycol) oleyl ether. Macromer initiators were also prepared from the reaction of 1 with PEG having Mω values of 200, 400, 600, 1000, or 1500 and with 4-vinylbenzyl chloride. The bulk polymerization of styrene by macroinimers gave crosslinked styrene-PEG block copolymers, while the polymerization by macroinitiators gave soluble copolymers. The molecular weights of the styrene-PEG block copolymers obtained with macroinitiators having either oleyl, benzoyl, or phenyl urethane end groups were 22000-29000 g/mol. DSC measurements showed that the crosslinked block copolymers had crystalline PEG units with melting transitions ranging from 11-37°C. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2603-2603 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1097-1103 
    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: Scotch pine, eastern spruce, and eastern beech samples sawed longitudinally were impregnated with a new type of polymerization mixture (macroinimer and styrene), leading to crosslinked block copolymers of styrene and poly(ethylene glycol). Weight gains of 36.37-91.13% were obtained after polymerization for 2 h. Water uptake of the polymerized wood was found to be 35.13-72.07% after a water soak test of 144 h. While spruce gave the highest uptake (72.07%), beech showed the lowest value (35.13%). The specimens impregnated with the mixture of macroinimer and styrene showed a water-repellent effectiveness of 35.14-58.15% after a water soaking test of 144 h. The highest values of water-repellent effectiveness were found for spruce, while the lowest values were obtained for pine. A maximum antiswell efficiency (ASE) of 42.43% was obtained for spruce, followed in order by beech and pine, respectively. The ASE value increases with an increase in wt % gain. Improvements of 19.12% in longitudinal compression and 25% in bending strength were also achieved for spruce samples with low weight percent gain. IR spectroscopy was used for chemical characterization of the wood-polymer composite. © 1993 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1415-1426 
    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: α,ω-Amine terminated organofunctional polydimethylsiloxane (PDMS) was condensed with 4,4′-azobis-4-cyanopentanoyl chloride (ACPC) to prepare macroazoinitiators containing siloxane units. Interfacial polycondensation reaction at room temperature was applied: ACPC was slightly dissolved in carbon tetrachloride and it was poured on aqueous NaOH solution of PDMS. Block copolymers containing PDMS as a block segment combined with polystyrene (PS) have been derived by the polymerization of styrene monomer initiated by these macroazoinitiators. PS-b-PDMS block copolymers were characterized by using nuclear magnetic resonance and infrared spectroscopy. Thermal and mechanical properties of the block copolymers were studied by using thermogravimetric analysis, differential scanning calorimetry, and a Tensilon stress-strain instrument. The morphology of block copolymers was investigated by scanning electron microscopy. PDMS-g-polybutadiene (PBd) graft copolymers were also prepared by reaction of PBd with the above macroazo-initiator. Increase in the amount of macroazoinitiator in the mixture of PBd (52% w/w) leads to the formation of crosslinked graft copolymers. Molecular weights of soluble graft copolymer samples were between 450 and 600 K with a polydispersity of 2.0-2.3. © 1996 John Wiley & Sons, Inc.
    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 60 (1996), S. 2141-2147 
    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: Poly(glycidyl azide) (PGA) an energetic polymer and polyepichlorohydrin (PECH) were condensed with 4,4′ azobis(4-cyanopentanoyl chloride) (ACPC) to prepare macro-azo-initiators. Block copolymers containing each of these polyethers as a block segment combined with polystyrene (PS) or poly(vinyl acetate) (PVAc) have been drived by the polymerization of monomers initiated with this macro-azo-initiators. Thermal properties of block copolymers were investigated with differential scanning calorimetry (DSC) and thermogravimetry. DSC traces showed single glass transition temperatures in between the related segments of copolymers. Dynamic thermogravimetric analysis revealed the individual degradation behaviors of block segments © 1996 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 1515-1524 
    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: Polystyrene-PEG crosslinked block copolymers were prepared from styrene copolymerization by either poly(ethylene glycol dimethymethacrylate) (PEG-DM) or macronomer initiators (MIM). Mw values of PEG of PEG-DM were 400, 600, 1000, 1500, 3000, 10,000, and 35,000, and of MIM, 400 and 1500. Swelling in H2O or CHCl3 of the sulfonated and unsulfonated block copolymers were determined under comparable conditions and found to be vary significantly. The ion-exchange capacity and selectivity coefficients of these ionexchange resins were investigated. The capacities of the obtained ion exchangers were varied between 0.4 and 2.9 meq/g. © 1996 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1313-1320 
    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: Polystyrene-poly(β-hydroxynonanoate) (PS-PHN) graft copolymers having 12, 17, 27, 31, 37, 60, 89, and 94% PS contents were prepared using active PS synthesized from styrene and oligododecandioyl peroxide initiator. Then the copolymer films were cast from chlo-roform, toluene, cyclohexanone, and butyl acetate. PS and PHN homopolymer blends were also prepared as films having 8, 12, 28, 34, 44, and 64% PS in the same casting solvents. The contact angles of water, glycerol, ethylene glycol, formamide, trans-decaline, and paraffin oil drops were measured on these cast films. The contact angle results were evaluated in terms of surface free energy components using Van Oss-Good methodology. It was determined that the Lifshitz-van der Waals component (γLWs) of the graft copolymers and blend of homopolymers did not differ so much with the copolymer composition. However, the electron donor component of the surface free energy (γ-s) decreased with the decrease of PHN content to a considerable extent. It was observed that this decrease is more linear than that of homopolymer blends. The effect of the nature of the casting solvents on the surface properties of the polymers was also investigated in terms of their solubility parameter values and it was found that the more H-bonding solvents resulted in higher (γ-s) surfaces. © 1996 John Wiley & Sons, Inc.
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