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  • Wiley  (2)
  • 1980-1984  (2)
  • Jewish studies  (2)
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  • Wiley  (2)
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  • 1980-1984  (2)
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  • Jewish studies  (2)
  • 1
    In: Israel Journal of Chemistry, Wiley, Vol. 22, No. 2 ( 1982-01), p. 168-172
    Abstract: Photochemical water splitting (H 2 O → H 2 + 1/2O 2 ) has been shown to occur on UV irradiation of aqueous suspensions of strontium titanate, modified by surface photodeposition of rhodium species. 7 Further improvement of the catalytic materials has now been achieved, using thermal deposition techniques. The most active material, prepared by heating rhodium chloride impregnated SrTiO 3 powder at 500°C in air, allowed one to produce appreciable quantities of (H 2 + 1/2O 2 ) gas and to reach high turnover numbers on the catalytic material. The photolysis efficiency presents a strong pH dependence with an optimum around pH ∼ 14 and increases markedly when the wavelength of the light decreases from 400 to 300 nm. The amount of rhodium deposited also has a marked effect with an optimum at about 0.2–0.3% Rh by weight. ESCA studies have provided information about the nature of the catalytic deposit and about its relation to the activity of the materials. Catalytic efficiency and mechanistic aspects are discussed. The oxidation state of the rhodium species has a drastic influence: whereas SrTiO 3 loaded with reduced rhodium shows no catalytic activity, the efficiency increases on progressive oxidation of the deposited metal to surface rhodium(III) species, as detected by ESCA. The photoactive step may involve both band‐gap excitation of the semi‐conductor support and direct UV excitation of the deposited Rh(III) species.
    Type of Medium: Online Resource
    ISSN: 0021-2148 , 1869-5868
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1982
    detail.hit.zdb_id: 2066481-3
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  • 2
    Online Resource
    Online Resource
    Wiley ; 1981
    In:  Israel Journal of Chemistry Vol. 21, No. 2-3 ( 1981-01), p. 145-150
    In: Israel Journal of Chemistry, Wiley, Vol. 21, No. 2-3 ( 1981-01), p. 145-150
    Abstract: In order to study the stereochemistry of thiirane oxide decomposition, syn ‐ and anti ‐2,3‐dideuterothiirane‐1‐oxides and trans ‐2,3‐dideutero‐thiirane‐1‐oxide have been synthesized in three steps from cis ‐ and trans ‐dideuteroethylene via stereospecific formation of the corresponding oxiranes and thiiranes. The presence of the deuterium label was used so as not to perturb the course of the decomposition from that of the parent thiirane oxide. Pyrolysis of the labeled thiirane oxides in both gas and solution phase proceeded with greater than 90% retention of stereochemistry. Analyses were performed by comparison of the infrared spectra of the product mixtures with standard calibrated samples. Attempts to trap possible biradical intermediates with di(p‐anisyl)thioketone gave a low yield of products, possibly derived from addition to thiirane oxide. These results suggest a possible partial contribution of a biradical mechanism to the thiirane oxide decomposition. If bond rotation in the biradical is slow, this mechanism could be the sole mode of sulfur monoxide extrusion.
    Type of Medium: Online Resource
    ISSN: 0021-2148 , 1869-5868
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1981
    detail.hit.zdb_id: 2066481-3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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