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  • 1
    ISSN: 1432-0649
    Keywords: 42.60 ; 42.55
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Conclusion We have demonstrated the existence of an anomalous polarization coupling mechanism present in the injection locked TEA CO2 laser. As a direct consequence of this work, a new injection technique has been formulated which permits efficient injection coupling and maximises energy extraction whilst eliminating the detrimental optical feedback effects to which other injection locking systems are prone.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0649
    Keywords: 42.55 ; 42.60
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We report a comparative study of a pulsed as well as continuous-wave (cw) injection seeding of a Ti:Sapphire laser pumped by aQ-switched frequency-doubled Nd3+:YAG laser for achieving narrow spectral bandwidth. The results have indicated that the Ti:Sapphire laser using either a pulsed or a cw injection seeding could achieve efficient energy extraction in a narrow spectral bandwidth. In the case of pulsed injection seeding, the injection energy required for the complete injection seeding critically depended upon the timing of the Ti:Sapphire laser with respect to the delayed onset of the slave laser. On the other hand, in the case of cw injection seeding, the spectral bandwidth of the Ti:Sapphire laser was efficiently narrowed down to approximately 0.01 cm−1 with an injection power of less than 1 mW. In both types of injection seeding, characteristics observed experimentally were compared with those obtained by a numerical simulation code based on the one-dimensional rate-equation model.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 26 (1984), S. 412-418 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Pyridoxaminephosphate oxidase (EC 1.4.3.5, deaminating) that was partially purified about 40-fold from dry baker's yeast was immobilized to iodo- and bromoacetyl polysaccharides. The most effective carrier was an iodoacetyl cellulose, to which almost complete activity of pyridoxine 5′-phosphate oxidase was immobilized in 0.02M potassium phosphate buffer (pH 8.5) containing 2M ammonium sulfate at 4°C. The immobilized enzyme was more stable than the purified, soluble enzyme against heat and pH change. It was confirmed that N-(5′-phosphopyridoxyl)-L-serine was degradedly oxidized to pyridoxal 5′-phosphate and L-serine by the immobilized enzyme as comparable rate as pyridoxine 5′-phosphate, whereas N-(5′-phosphopyridoxyl)-D-serine did not serve as substrate, as in the purified, soluble enzyme.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 3311-3325 
    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: Radiation-induced polymerization of water-saturated styrene (water content 3.5 × 10-2 mole/liter) was carried out in a wide range of dose rate between 1.2 × 103 and 1.8 × 107 rad/sec, and compared with the polymerization of the moderately dried styrene (water content 3.2 × 10-3 mole/liter). Molecular weight distribution curves of the polymerization products showed that they were generally consisted of four parts, namely, oligomers, radical, cationic, and super polymers. Contributions of the four constitutents to the polymerization and the number average degrees of polymerization (DP) of the four kinds of polymers were calculated by the graphical analysis of the curves. The rate of radical polymerization and DP of radical polymers are independent of the water content; the dose rate dependences of the polymerization rate and DP agree with the well known square root and inverse square root laws, respectively, of the radical polymerization of styrene. The rate of ionic polymerization is directly proportional to the dose rate, but it decreases, at a given dose rate, inversely proportional to the water content of styrene. DP of ionic polymer is independent of the dose rate but decreases with increasing water content. The super polymer of DP about 104 is not formed in the case of the moderately dried styrene. G values for the initiating radical and ion formation are calculated to be, independently of the dose rate and water content, 0.66 and 0.027, respectively. It was suggested that oligomer was formed in the early stage by the interaction of cation with anion and only those cations which had survived underwent polymerization.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 2683-2693 
    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: A kinetic equation was derived for the radiation-induced polymerization of styrene under the assumption that both radical and cationic polymerizations take place concurrently throughout the whole range of the dose rate of radiation and the water content of the styrene. The equation enables one to calculate rates of the total, radical, and cationic polymerization at a given dose rate and water content and agrees satisfactorily with experimental results, which cover dose rates from 4.2 × 10 to 2.1 × 105 rad/sec and water contents from 3.2 × 10-3 to 3.5 × 10-2 mol/l. Experimental estimation of the contribution of radical and cationic mechanisms was done by GPC curves of polymers obtained under various conditions. When the contribution of ionic mechanism is expressed in weight percent, it changes from 0% to 100% in the range of the experiment; on the other hand, if it is expressed in mole percent, it is independent of the dose rate and remains constant throughout the whole range of the experiment.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 108-109 
    ISSN: 0935-6304
    Keywords: Ion-exchange liquid chromatography ; Acid phosphatase ; Alkaline phosphatase ; Chemistry ; Analytical Chemistry and Spectroscopy
    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
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 9 (1986), S. 479-480 
    ISSN: 0935-6304
    Keywords: High-performance liquid chromatography, HPLC ; Alkaline phosphatase, AP ; Lactate dehydrogenase, LD ; γ-Glutamyltransferase ; γ-GT ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On décrit comment la méthyl-5-diphényl-6,7-tétrahydro-5,6,7,8-ptérine s'autoxyde en milieu alcalin en utilisant un atome-équivalent d'oxygène pour former l'hydroxy-4a-méthyl-5-tétrahydroptérine quinolique correspondante. L'oxydation est catalysée par Fe3+, qui forme d'abord un complexe avec la tétrahydroptérine. Dans ce complexe un électron est transféré de la tétrahydroptérine sur le fer. Un mécanisme radicalaire d'oxydation des tétrahydroptérines, basé sur ces données expérimentales, est proposé et discuté.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 50 (1967), S. 411-416 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By oxydation of N(5)-methyl-6,7-diphenyl-5,6-dihydro- and N(5)-methyl-6,7-diphenyl-5,6,7,8-tetrahydro-pterine derivatives with perhydrol 8-monohydro- and 6,7,8-trihydro-pteridine radical cations are produced which are sufficiently stable for detection and structural elucidation by ESR. hyperfine analysis. The biological implications of these radicals for pteridine dependent hydroxylation and methyl transfer from 5-methylfolinic acid are discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: En milieu acide la méthyl-5-diphényl-6, 7-dihydro-5, 6-ptérine perd rapidement son reste méthyle et un H pour être transforméee en diphényl-6, 7-ptérine. Il semble qu'un des produits intermédiaires de la transformation soit la méthyl-5-diphényl-6, 7-dihydro-5, 8-ptérine. On suppose qu'à partir de cette ptérine il se forme un radical-cation perdant spontanément un proton en N(8) et le radical méthyle, phénomène qui pourrait bien être lié à la transéthylation biologique catalysée par les méthyl-5-ptérines hydrogénées.
    Type of Medium: Electronic Resource
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