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  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 20 (1993), S. 949-954 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Transmission Móssbauer spectra of binary coprecipitated nickel(II)-iron(III) hydroxides (molar ratios 9:1 and 4:1) are analysed and compared with the results of AES analyses of their surface composition. A correlation between the data of the above techniques has been noted, indicating a redistribution of the components (i.e. Ni and Fe) in the surface layers, the latter being enriched with iron(III) as compared to the bulk. The results obtained are in good agreement with an excellent electrocatalytic activity of composite Ni-Fe hydroxide systems towards anodic oxygen evolution in alkaline electrolytes, taking into account a distinctly exhibited ‘surface’ electrocatalytic effect of ferric species on the nickel hydroxide electrode in the anodic oxygen evolution process revealed previously. Transmission Móssbauer spectroscopy has been shown to be a highly effective probe sensitive both to various bulk and surface effects related to the solid phases studied.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 2 (1993), S. 929-938 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The main factors determining molar mass characteristics of copolymers formed in nonterminating copolymerization under the conditions of chain transfer to solvent are studied theoretically. The dependences of the mean polymerization degrees on conversion and monomer feed composition for various values of reactivity ratios are obtained. The results obtained greately differ from those for homopolymerization. This is explained by the contribution of cross-propagation reactions. In particular, it is shown that at ≪ and ≪ the azeotropic copolymerization proceeds like the living one even if homopolymerization of each monomer is accompained by extensive chain transfer to solvent.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 1 (1992), S. 321-331 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new theoretical consideration of chain transfer to monomer in the anionic polymerization of hydrocarbon monomers is presented. It is shown that the kinetic scheme used in theoretical studies reported previously contradicts the widespread views on the chemical mechanism of carbanionic reactions. It is suggested that the most probable path of the transfer reaction is the proton abstraction from the side group of the monomer; the terminal double bond of the monomer molecule remains unchanged, and therefore the intermediate species can participate in succeeding reactions as a macromonomer. The molecular characteristics of polymer formed in processes with monomer transfer by side-group substitution are determined. At high conversion, the polymer formed in such a process is shown to possess a number-average degree of polymerization, P̄n, approaching the theoretical value for living polymers, and a P̄w exceeding it the more the higher the intensity of transfer. Furthermore, it shows a broad molecular weight distribution and a fairly noticeable degree of branching. These results considerably differ from those previously reported.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1040-0397
    Keywords: Enzymatic methods ; Enzymes inhibition ; Acetylcholinesterase ; Butyrylcholinesterase ; Organophosphorus ; pesticides ; Pesticides assay ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Disposable conductometric microbiosensors based on immobilization of acetyl and butyrylcholinesterases (BuChEs) on interdigitated electrodes were fabricated. Enzymes were immobilized by crosslinking with bovine serum albumin and the differential output between the pair of electrodes covered with the enzyme membrane and the pair covered with albumin only was recorded. On the basis of these biosensors, a biochemical assay for pesticides in liquids was developed. Respective detection limits were 5 × 10-11 M for diisopropyl fluorophosphate (DFP), 10-7 M for trichlorfon, and 10-6 M for paracoxon-methyl and paraoxon-ethyl for the assays based on the enzymes tested. The presence of pesticides in the sample in concentration exceeding the detection limits can be detected after only 10 minutes of incubation, whereas, in order to extend the range of the determined pesticide concentration and to improve the accuracy of the assay, it is better to use incubation times longer than 30 minutes. Use of pyridin-2-aldoximide methiodide as reactivating agent allowed one to achieve the complete recovery of the sensor response when it was incubated in low-concentrated pesticide solutions, e.g., less than 10-6 M for paraoxon-methyl and during a short time, e.g., 10 to 20 minutes, for 10-5 M paraoxon-methyl solution.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Mössbauer parameters for ferric hydroxo forms in alkaline matrices, ferric oxyhydroxide and its admixture at the nickel hydroxide electrode surface as well as for ferric hydroxo species absorbed at nickel hydroxides from strongly alkaline solutions have been compared. The feasibility of transmission Mössbauer spectra acquisition for the adsorbed species in the presence of dissolved forms (e.g. in situ) is based on the principle that the latter give no Mössbauer effect at room temperature owing to their diffusional mobility, while the former, being fixed at the adsorbent surface, have been shown to exhibit a sufficient resonant absorption. The effects of adsorption and water have been noted. Some questions connected with anodic oxygen evolution electrocatalysis by iron species involved in the anodic process at the nickel hydroxide electrode are also discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 7 (1969), S. 829-834 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 985-995 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of methyl acrylate in water and in dilute, aqueous, soap solutions, initiated by potassium peroxydisulfate, has been investigated, a dilatometric method being used to follow the conversion. It has been shown that small amounts of an anionic soap increase the rate of reaction while a cationic soap has the reverse effect. The change of molecular weight with conversion has also been examined as well as the effect of the exclusion of oxygen from the system.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 1833-1839 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of acrylamide in aqueous surfactant solutions, initiated by potassium persulfate, has been investigated, dilatometry being used to follow the conversion. It has been shown that below the critical micellar concentration (CMC), cationic, anionic and non-ionic surfactants have no effect, while above the CMC only cationic soaps have an effect, lowering both the rate of polymerization and the molecular weight of the resultant polymer.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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