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Selective Oxidation of Toluene to Benzaldehyde: Investigation of Structure-Reactivity Relationships by in situ-Methods

机译:苯甲醛的选择性氧化苯甲醛:原位方法对结构 - 反应性关系的研究

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(VO)_2P_2O_7 and potassium-doped V_2O_5 catalysts have been studied in the selective oxidation of toluene to benzaldehyde by in situ-EPR, -FTIR, -XRD, -UV/VIS and -XPS. In (VO)_2P_2O_7, Bronsted surface sites formed under reaction conditions favour strong product adsorption and, thus, total oxidation. They can be blocked by adding pyridine, which improves catalystic performance. K-V_2O_5 catalysts are markedly reduced during reaction. Both V~(5+) and V~(4+) species are likely to be active in the catalytic redox cycle. Crystalline K_0.5V_2O_5 formed on the catalyst surface under feed probably lowers the catalytic performance due to structural reasons.
机译:(VO)_2P_2O_7和耐钾掺杂的V_2O_5催化剂已经在原位-EPR,-FFR,-XRD,-UV / VI和-XPS中选择性氧化于苯甲醛至苯甲醛。在(VO)_2P_2O_7中,在反应条件下形成的伪造表面位点有利于强产品吸附,因此,总氧化。它们可以通过加入吡啶来阻止,这提高了催化性能。反应期间K-V_2O_5催化剂显着降低。 V〜(5+)和V〜(4+)种类均在催化氧化还原循环中可能有效。在饲料的催化剂表面上形成的结晶K_0.5V_2O_5可能导致结构原因降低催化性能。

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