ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Publication Date: 1956-03-01
    Print ISSN: 0022-3654
    Electronic ISSN: 1541-5740
    Topics: Chemistry and Pharmacology , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 1957-05-17
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 1960-05-27
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 60 (1956), S. 267-269 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 18 (1988), S. 619-624 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A novel system has been examined in which the charging cycle of a rechargeable cell was photoassisted. Rechargeable cells comprised of ap-type InP semiconductor anode coated with a polyanthraquinone redox polymer film and a polypyrrole-coated Pt cathode immersed in 0.1 M TEAP/CH3CN were photoelectrochemically charged and then discharged in the dark. These systems showed no degradation of electroactivity after 25 cycles. The charge storage capacity and the effectiveness of the photoassistance is limited by incomplete electroactivity of the redox polymer film and the small photovoltages generated by thep-InP/polyanthraquinone electrode. The role of Fermi level pinning in limiting the performance is assessed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 97-107 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Lifetimes of polymer radicals were determined by a direct flow technique. The variation of yield of polymer with the period between initiation by an ultraviolet source and destruction in an inhibitor solution was determined by spectrophotometric analysis. A swiftly falling stream of monomer was irradiated by a sharply focussed beam of intense ultraviolet radiation, and the time of radical growth was controlled by varying the distance of fall at a constant flow rate. The variation of yield of polymer with the time interval between photochemical initiation an destruction in an inhibitor solution was determined by spectrophotometric analysis of the polymer formed. A polished elliptical reflector was used, instead of the customary quartz lenses, with the source and stream at the foci of the ellipse. A water-jacketed capillary was employed to eliminate spurious thermal initiation. Radical lifetimes of 0.24 seconds for styrene and 1.80 seconds for butyl acrylate were obtained. The data were compared with values calculated on the basis of non-stationary state kinetics in a flow system.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 359-364 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Block copolymers of butyl acrylate-styrene and butyl acrylate-2-vinyl pyridine were prepared in a flow system. An intense ultraviolet source was focussed on a stream of monomer falling into a second monomer. The period between photochemical initiation in the stream and block polymer formation was controlled by varying the flow rate and distance of fall. By application of nonstationary state kinetics the yield of polymer in the stream was calculated and compared with the experimental yield determined spectrophotometrically. A comparison was made of the composition of random copolymer based on the copolymerization equation and that determined experimentally. The yields and compositions of the products showed that the desired block copolymers had been formed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 46 (1960), S. 139-149 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the polymerization of methyl methacrylate in the presence of p-benzoquinone were investigated. The course of the reaction was followed by dilatometry and with tracer methods. Alternate experiments were performed C14-tagged azobisisobutyronitrile initiator and inactive p-benzoquinone and, alternatively, radioactive initiator and inactive retarder being used. These data, coupled with number average molecular weights determined by osmometry, served to determine the number of fragments of initiator and retarder incorporated per polymer molecule. It was found that the reaction was retarded at low concentrations of p-benzoquinone but showed a definite transition to inhibition at higher concentrations. Analysis of the data showed that the number of initiator fragments incorporated per polymer molecule was independent of retarder concentration, but that the number of retarder molecules per polymer molecule increased. The results indicate that the rate of chain initiation decreases with retarder concentration until inhibition is observed. The data are interpreted on the basis of interaction of benzoquinone with primary radicals generated by the initiator. The results also furnish distinct evidence against the acceptance of copolymerization or chain transfer as significant steps in the reaction mechanism.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 817-823 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dimethylaniline (DMA) induces chain transfer in the zinc bromide-complexed donor-acceptor polymerizations of styrene-acrylonitrile to form alternating copolymers. The Mayo plots are linear, but the rates decrease with increase in DMA and degradative chain transfer occurs. Although conventional free-radical transfer agents have negligible effect on the rates or molecular weights, a twentyfold reduction of molecular weight is obtained with DMA. Spectroscopic data indicate the formation of an equimolar complex of DMA and ZnBr2, but the lowering of molecular weight is not attributable to the reduction of the effective ZnBr2, concentration. A possible mechanism involving a competition between [ZnBr2(DMA)2] and [ZnBr2,DMA,AN] is suggested.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2639-2647 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate and molecular weight profiles were obtained for the spontaneous alternating copolymerizations conducted with diethylaluminum chloride. The rate formally fitted an expression, R = kp[MMA][Sty], and the rate constant was established by two distinct methods: (1) from the yield versus time data and (2) from initial rate over a range of initial concentrations; it was determined as 5.4 × 10-6 l./mole-sec with Ea = 4.2 kcal/mole. Molecular weights were determined by gel-permeation chromatography. No increase in molecular weight was observed with increased reaction time. Thus living centers or diradicals are not involved in the process. The M̄n shows a steady decrease with increase in monomer-diethylaluminum chloride concentration but the rate is maximum at equimolar monomer concentrations. The data are interpreted on a chain-transfer mechanism and show close agreement to a model in which the excess complexed acceptor monomer is the transfer agent. The chain-transfer constant of 7.1 × 10-4 l./mole-sec is several orders of magnitude greater than for uncomplexed systems.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...