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Novel Method for Preparation of ISSanostrocturecl AU/HG2 on S1O2 Support by Colloidal Synthesis

机译:用胶体合成制备issanostrocturecl Au / hg2的新方法

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The formation of Au/TiC>2 nanostructured interface on SiC>2 support using Au hydrosol and Ti-isopropoxide or Ti(IV)-bis(ammonium lactato) dihydroxide (TALH) precursors has been investigated in context of preparing a novel type of catalysts active in the CO oxidation. Different preparation routes were compared: (i) Au sol was modified by Ti-precursor then adsorbed on silica followed by calcination, (ii) Au/silica was modified by Ti-precursor and calcined, (iii) Au was deposited on S1O2 modified by Ti-precursor and calcined. The enhanced catalytic activity in the CO oxidation compared to that of the analogue anatase supported Au catalyst is possibly due to several factors, such as, the morphology of TiO2 (likely amorphous) and formation of Ti-O-Si interaction, which results in the formation of large and efficient interface between Au and TiO2 This was supported by examination of the mechanical mixtures of SiO2 and anatase supported Au catalysts as well as their modified alternatives.
机译:在制备新型催化剂的背景下研究了使用Au Hydrosol和Ti-异丙氧化钛或Ti(乳酸铵)二羟基氧化物(盐酸盐)二羟基氧化物(盐酸盐)的Au / TiC> 2纳米结构界面的形成活跃在共同氧化。比较了不同的制备途径:(i)通过Ti-prepareors改性Au溶胶,然后在二氧化硅上吸附,然后通过煅烧,通过Ti-precearor(II)修饰Au /二氧化硅并煅烧,(III)在S1O 2上沉积(III)Au被修饰Ti-preparsor和煅烧。与模拟亚脱酶支持的Au催化剂相比,共同氧化的增强催化活性可能是由于若干因素,例如TiO 2(可能是无定形)的形态和Ti-O-Si相互作用的形态,这导致了通过检查SiO 2和Anatase支持的Au催化剂的机械混合物以及其改性替代方法,支持Au和TiO 2之间的大型和有效接口的形成。

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