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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 10 (1979), S. 325-328 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Фотоадсторбция кислорода в области примесного поглощения рутила зависит от степени гидратации поверхности, а максимум активности расположен вобласти собственного поглощения. Фотоадсорбция CO наблюдается в области собственного поглощения.
    Notes: Abstract Oxygen photoadsorption in the range of impurity absorption of rutile is governed by the surface hydration. The activity maximum is in the region of intrinsic absorption, where carbon monoxide is photoadsorbed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 10 (1979), S. 329-332 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract В области собственного поглощения рутила реакция окисления CO протекает по окислительновосстановительному механизму через взаимодействие CO с ион-радикалами O−, причём фотокаталитическая активность определяется плотностью 2р-состяний у потолка валентной зоны.
    Notes: Abstract In the region of intrinsic rutile adsorption, CO oxidation follows a redox mechanism via the interaction of CO with O− ion-radicals, and the photocatalytic activity is determined by the density of 2p states close to the top of the valence band.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 11 (1979), S. 103-106 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Методом ЭПР исследовано образование и свойства ион-раднкалов O 2 − и [O−·O2], возникающих при Фотообпучении окисленного анатаза. Показана ропь Физически адсорбированного кислорода в процессе разделения электрон-дырочных пар.
    Notes: Abstract ESR studies on the formation and properties of O 2 − and [O−·O2] ion-radicals under photo-irradiation of oxidized anatase have been performed. The role of physically adsorbed oxygen in the separation of electrone-hole pairs is shown.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 11 (1979), S. 107-111 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Методом ЭПР изучена адсорбция O2 на восстановленном анатазе. Показано, чко количество наблюдаемых O 2 − связано с наличием адсорбированного кислорода на поверхности, а их параметры можно изменять адсорбцией молекул CO.
    Notes: Abstract ESR studies of O2 adsorption on reduced anatase have been performed. The amount of O 2 − species is determined by adsorbed surface oxygen and their parameters are changed by CO adsorption.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 11 (1979), S. 221-224 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Изучены свойства парамагнитных центров, специфичных для восстановленного анатаза: $$\boxed{O^ - }$$ (g1=1,999, g2=1,984, g3=1,979) и $$\boxed{O_3^ - }$$ (g1=2,046, g2=2,008), связанных со стабилизацией фотоиндуцированных дырок вблизи анионных вакансий. На восстановленном окисле обнаружен новый тип фотоадсорбции O2 при hν〉1 эв, связанный с генерацией на поверхности только электронных центров.
    Notes: Abstract The paramagnetic centers of reduced anatase $$\boxed{O^ - }$$ (g1=1.999, g2=1.984, g3=1.979) and $$\boxed{O_3^ - }$$ (g1=2.046, g2=2.008), assigned to the stabilization of photoinduced holes near anion vacancies, have been studied. For the reduced oxide a new type of O2 photoadsorption at h ν〉1 eV due to the generation of only electron surface centers has been discovered.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 11 (1979), S. 235-239 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Методом ЭПР показано, что низкотемпературное фотовосстановление анатаза в CO имеет место как в области собственного, так и примесного поглощения окисла и сопровождается образованием анионных вакансий. Последующее облучение в присутствии O2 приводит к образованию кислородных комплексов O 3 − , связанных с наличием анионных вакансий.
    Notes: Abstract ESR studies show taht the low temperature photoreduction of anatase in CO proceeds in both the fundamental and impurity light absorption regions of the oxide, leading to anion vacancies. Further irradiation in the presence of O2 leads to $$\boxed{O_3^ - }$$ complexes, assigned to anion vacancies.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 11 (1979), S. 277-280 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Показано, что центры $$\boxed{O^ - }$$ (g1=1,999; g2=1,984; g3=1,979), обусловленные стабилизацией фотоиндуцированных дырок O− на координационно ненасыщенных ионах Ti4+, не взаимодействуя с CO вплоть до 250° K являются центрами активации молекулярного кислорода в виде комплекса $$\boxed{O_3^ - }$$ (g1=2,046; g2=2,008) в реакции окисления CO даже при 87°K с образованием CO 3 − (g‖=2,0285) g⊥=2,0055).
    Notes: Abstract The $$\boxed{O^ - }$$ centers (g1=1,999; g2=1.984 and g3=1.979) assigned to the stabilization of photoinduced O− holes on coordinatively unsaturated Ti4+ ions, not interacting with CO up to 250 K, are shown to be the activation centers of the molecular oxygen as an $$\boxed{O_3^ - }$$ complex (g1=2.046; g2=2.008) for CO oxidation even at 87 K with the formation of CO 3 − (g‖=2.0285, g⊥=2.005).
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 12 (1979), S. 1-4 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Методом ЭПР исследовано образование парамагнитных продуктов при фотооблучении в различных спектральных областях восстановленного анатаза с хемосорбированным O2 и в присутствии адсорбированной CO. Обнаружено образование ион-радикальных комплексов, интерпретируемых как CO 3 − и CO 2 − при энергиях квантов, соответственно, 2,8 и 3,4 эв.
    Notes: Abstract ESR studies have been carried out to investigate the formation of paramagnetic products under photo-irradiation in various spectral regions of reduced anatase with chemisorbed O2 and adsorbed CO. Ion-radical complexes interpreted as CO 3 − and CO 2 − , are formed at quantum energies of 2.8 and 3.4 eV, respectively.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 13 (1980), S. 437-437 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 18 (1981), S. 321-324 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Показано, что фотодсордция кислорода на SnO2 сопровождается образованием анион-радикалов O 2 − . Наиболее эффективно процесс разделения зарядов при освещении и стабилизации фотоиндуцированных центров происходит в пр. сутствии физически адсордированного O2.
    Notes: Abstract Oxygen photoadsorption on SnO2 is shown to be accompanied by the formation of O 2 − ion-radicals. Charge separation under irradiation and stabilization of photoinduced centers is mot effective in the presence of physically adsorbed O2.
    Type of Medium: Electronic Resource
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