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首页> 外文期刊>Russian Journal of General Chemistry >Structural-Chemical Activity Criteria for Catalysts of Deep Oxidation
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Structural-Chemical Activity Criteria for Catalysts of Deep Oxidation

机译:深度氧化催化剂的结构化学活性标准

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The problem of the determination of the structural-chemical criteria of the redox-catalysts activity evaluation remains one actual for theory and practice of the catalysts synthesis. In the present work we used the industrial domestic catalysts AP-64 (0.62 wt % Pt on an aluminum γ-oxide), catalyst of production of the "Walker" company (USA) (0.2 wt % Pt on a cordierite carrier), and analytically pure cor-dierite. The data of the high resolution IR spectroscopy [1] and analysis of the oxygen thermal desorption [2] made it possible to reveal the special features of the electron-excited states and the factors, which cause the catalytic action. The spectrum of the most active platinum contact shows that the significant modification of the carrier surface in the process of the catalyst preparation, which is accompanied with the notable decrease in the specific surface area (86->18 m~2 g~(-1)), does not practically change the characteristic intensive IR- emission bands (1750, 1370, 1240, and 1050 cm~(-1)) that indicates the localization of the processes of cooperative interaction of the excited states in the bulk.
机译:确定氧化还原催化剂活性评估的结构化学标准的问题仍然是催化剂合成的理论和实践中的一个实际问题。在当前工作中,我们使用了工业家用催化剂AP-64(在γ-氧化铝上的Pt为0.62 wt%),“ Walker”公司(美国)生产的催化剂(在堇青石载体上的Pt为0.2 wt%)和分析纯的堇青石。高分辨率红外光谱数据[1]和氧气热脱附分析[2]使得揭示电子激发态的特殊特征和引起催化作用的因素成为可能。活性最高的铂接触光谱表明,催化剂制备过程中载体表面发生了明显的修饰,比表面积显着减小(86-> 18 m〜2 g〜(-1) ))并没有实际改变特征性强烈的IR发射带(1750、1370、1240和1050 cm〜(-1)),这表明本体中激发态的协同相互作用过程的局部化。

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