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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 32 (1983), S. 1105-1107 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. The radiolysis of a series of individual perfluorinated compounds leads to the formation of radicals which are stable not only in the liquid phase in solutions but also in the gas phase. 2. The discovered stable radicals do not react with oxygen either during prolonged storage or during γ irradiation at 300°K. 3. The radiolysis of the compounds in the liquid and solid phases leads to the formation of various unstable radicals.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 32 (1983), S. 1318-1318 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. Strain brought about by external pressures up to 6 kbar does not cause spontaneous initiation of the autowave process, which does not conform to the conception of the definite role of strain in the presumed mechanisms of chemical reactions in the systems investigated. 2. Strengthening the systems under pressure leads to a reduced rate of propagation of the reaction front, and an increase in the inert heating zone, which verifies our previous discovery of the mechanism of the autowave process, showing an exactly opposite effect on the interaction between the destruction of the sample and the chemical reactions.
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  • 4
    ISSN: 1573-9171
    Keywords: solid hydrogen cyanide ; photolysis ; radiolysis ; free radicals ; ions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The photolysis of solid hydrogen cyanide and the effects of UV light on60Co-γ-irradiated HCN at 77 K were studied using an ESR technique. As in the case of radiolysis, the HZ2C=N radical formed due to “sticking” of the H atom to the triple bond of the HCN molecule is the main radical product of low-temperature HCN photolysis. The C=N− radicals are accumulated at 77 K in insignificant amounts (≈3 %). It was established that radical and ionic products stabilized in y-irradiated HCN possess photochromism and under the action of UV light enter photochemical reactions leading to their decomposition. Upon photobleaching, the concentration of H2C=N− radicals first increases two- to threefold because of the decomposition of H2C=N− ions and then decreases. The presence of radicals and ions formed upon the low-temperature radiolysis of HCN broadens the optical absorption band of the system, and the boundary of the action spectrum shifts from 280 nm (for nonirradiated HCN) to the visible region at 400–440 nm.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1401-1416 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results of studying the radiation curing of methacryloyloxyalkyl carbonates (MC), a new type of oligomer, are presented. These oligomers are notable for their high rates of radiation curing. The radiation yield G(-M) is 2 × 105 for MC and 2 × 104 for triethylene glycol dimethyacrylate. The polymerization rate of MC appeared to be proportional, independent of the conversion degree, to the irradiation dose rate in the power of 0.9-1.0 (for dose rates ranging from 0.4 to 15 rad/s). In regard to the temperature dependence of the polymerization rate of MC for small conversion degrees, two temperature regions with different values of effective activation energy (18-20 kcal/mol and 2 kcal/mol, respectively) were observed. When an irradiated MC sample is being unfrozen, its polymerization occus in the region of devitrification (220-240°K). As distinct from mass polymerization, in the polymerization of MC solutions in acetone and benzol the mobility of growing chains increases so that the bimolecular termination becomes possible and the limiting conversion of double bonds is derived. Rather small irradiation doses necessary for curing MC and the proportionality of the radiation-induced polymerization rate to the dose rate make these oligomers valuable for various industrial applications.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1551-1558 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The γ radiolysis of solid C3O2 at 77 K produces paramagnetic centers of several types. The ESR spectrum constitutes a number of narrow lines with an anisotropic g factor. Some of the centers are photounstable and are lost after optical bleaching. Heating the sample results initially in the loss of photounstable centers and then, in the temperature region in which solid C3O2 undergoes a phase transition (140 K), loss of the centers responsible for the center section of the ESR spectrum. In the temperature region 140-270 K concentration of the centers remained at the level of 1015-1016 g-1. At higher temperatures an intense polymerization of liquid C3O2 followed by a sharp increase in concentration of the paramagnetic centers was observed. It is assumed that in radiolysis at 77 K and on subsequent heating the formation of oligomeric centers in solid C3O2 results in a decreasing probability of their loss. Using a calorimetric technique, we studied the kinetics of the postradiation polymerization of C3O2. Small additions of acetone (cationic inhibitor) brought about the loss of the oligomeric centers and suppressed completely all postpolymerization. The polymerization rate increased with the concentration of the resulting polymer. An autocatalytic character of the process is supposed to be connected with the formation of polymer-monomer complexes.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2331-2345 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Low-temperature postirradiation grafting of tetrafluoroethylene (TFE) to polyolefines and silicone elastomers was the subject of study. After preliminary dissolution of TFE in the polymer at 273°K the system was slowly cooled to 77°K. In this process a certain part of TFE in polyolefines (ethylene-propylene copolymer and polypropylene) is retained by the vitreous polymer matrix. When slowly heated after radiolysis at 77°K this system shows graft polymerization of dissolved TFE after Tg. The graft copolymer is soluble and its IR spectra contain absorption bands characteristic of polytetrafluoroethylene. In polydimethylsiloxane rubber (SKT) the dissolved TFE when frozen to 77°K remains sorbed between the SKT crystallites rather than in a separate phase. When these radiolyzed samples are heated the graft-polymerization occurs primarily over the temperature range between the TFE and SKT melting points. The technique provedes for 100-150% grafting of TFE. This method also permits grafting to silicone rubbers and to several other polymers and elastomers.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 287-294 
    ISSN: 1042-7147
    Keywords: Radiation ; crosslinking ; calorimetry ; polymer-monomer composition ; 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
    Notes: This work summarizes the results of a study of the mechanism of polymerization in monomer-polymer compositions initiated by ionizing radiation. Attention was mainly paid to the investigation of the polymerization directly in the γ-radiation field. The next monomers were chosen for monomer-polymer compositions: heptyl acrylate (HA), heptyl methacrylate (HMA) and some other acrylic and methacrylic monomers. The polymer components are: chlorinated polyethylene (CPE) (molecular mass Mn ≅ 1 × 105), chlorinated paraffins (CP) (molecular mass Mr ≅ 450), butadiene-nitrile rubber BN-1 (molecular mass Mw ≅ 3 × 105) and BN-2 (molecular mass Mw ≅ 2500). Compositions that are crosslinked (BN-1+HMA, BN-2+HMA, CPE+HA) and noncrosslinked under γ-radiation were specially selected. The dynamic of radiation polymerization in the system studied was measured by calorimetric technique. A calorimeter was situated directly in the zone of γ-ray60 Co. The dynamic of polymerization was followed by the heat release rate recorded by the calorimeter. Viscosity of the systems was measured on a rotational viscosimeter REOTEST-2 at room temperature. The investigations carried out have allowed us to establish the kinetic regularities of the radiation polymerization processes in the crosslinking and noncrosslinking compositions under irradiation based on HMA and some polymers. A comparison of the main characteristic of these processes was also made. The employment of the crosslinking and noncrosslinking polymers in the compositions significantly changes the radiation polymerization dynamics and allows the construction of the composites at the molecular level to be changed. The results obtained may serve as a basis for choosing the optimal system for producing-radiation-cured monomer-polymer compositions.
    Additional Material: 9 Ill.
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  • 9
  • 10
    Publication Date: 2020-02-01
    Print ISSN: 1070-4272
    Electronic ISSN: 1608-3296
    Topics: Chemistry and Pharmacology
    Published by Springer
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