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ZnS photocatalyst for hydrogen production, preparation therefor and method for producing hydrogen by use of the same

机译:用于制氢的ZnS光催化剂,其制备方法和使用该催化剂的制氢方法

摘要

The present invention relates to a novel photocatalyst, to preparing the photocatalyst and to a method for producing hydrogen in the presence of the photocatalyst. The novel photocatalyst of this present invention is characterized by the following formula IV: Pt(x)/ZnÄM(y)ÜS wherein "x" represents a percentage by weight of Pt in the photocatalyst ranging from 0.05 to 2.50; "M" is a promoter selected from the group consisting of V, Cr, Mo, Mn, Re, Ru, Os, Rh, Ir, Cu, Al and Ga; and "y" represents a mole % of M/(M+Zn) ranging from 0.01 to 20.00. The method for preparing the photocatalyst comprises the steps of: dissolving Zn-containing and M-containing compounds in water in such a way that M/(M+Zn) ranges, in mole %, from 0.01 to 20.00; adding H2S or Na2S as a reactant in the solution with stirring to precipitate ZnÄMÜS; washing the precipitate with water until pH reaches 7 and vacuum-drying the precipitate in a nitrogen(stream) atmosphere; adding Pt-containing compound to this precipitate in such a way that Pt ranges, in percentage by weight, from 0.05 to 2.50; illuminating the platinum-enhanced precipitate with ultraviolet light in a nitrogen atmosphere; washing the Pt-impregnated ZnÄMÜS thus obtained with water until the wash water pH reaches 7; vacuum-drying and then oxidation sintering the dried precipitate at from 280 to 420 DEG C for 1 to 3 hours, reduction sintering at the previously-sintered product at from 280 to 420 DEG C for from 1 to 3 hours.
机译:本发明涉及新型光催化剂,光催化剂的制备以及在光催化剂的存在下生产氢的方法。本发明的新型光催化剂的特征在于下式IV:Pt(x)/ZnÄM(y)ÜS其中“ x”表示光催化剂中Pt的重量百分比为0.05至2.50;和“ M”是选自V,Cr,Mo,Mn,Re,Ru,Os,Rh,Ir,Cu,Al和Ga的启动子; “ y”表示M /(M + Zn)的摩尔%,为0.01〜20.00。制备光催化剂的方法包括以下步骤:将含Zn和含M的化合物溶解在水中,使得M /(M + Zn)以摩尔%计为0.01至20.00;在搅拌下向溶液中加入H2S或Na2S作为反应物以沉淀ZnÄMÜS;用水洗涤沉淀物直至pH达到7,并在氮气(气流)气氛中真空干燥沉淀物;以这种方式将含Pt化合物加入该沉淀物中,使得Pt的重量百分比范围为0.05至2.50。在氮气氛下用紫外线照射增强铂的沉淀物;用水洗涤由此获得的浸有Pt的ZnÄMÜS,直到洗涤水的pH值达到7;真空干燥,然后氧化,将干燥的沉淀物在280至420℃下烧结1至3小时,在先前烧结的产物中在280至420℃下还原烧结1至3小时。

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