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Preparation of Crystalline OVO4 Catalyst by Soft Chemistry Technique and Application for Vapor-phase Oxidation of Picolines

机译:软化学技术制备结晶型OVO4催化剂及其在二甲酚的气相氧化中的应用

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摘要

A series of Cr-V mixed oxide catalysts (CrVO4, Cr_(1-x)Al_xVO4 and CrV_(1-x)P_xO4) have been prepared by "soft chemistry" technique. By mixing the aqueous solution of the raw materials and controlling the pH value, chromium vanadates (CrVO4-I and HI) were prepared as the pure orthovanadate crystalline form. Prepared chromium vanadates were employed in the vapor phase oxidation of 2-, 3-, and 4-picolines in order to investigate the relationship between the catalysis and structure of chromium vanadate. CrVO4-I (monoclinic) showed much higher activity than CrVO4-III (orthorhombic), suggesting that the bridging oxygen in the V-O-Cr bond is responsible for the catalytic activity. When a part of Cr or V was replaced with Al or P without changing the CrVO4-I type structure, the activities were enhanced. The acidity increased by the replacement of Cr with Al and V with P in CrVO4-I, resulting in the accelerating desorption of products. A partial replacement of V with P significantly improved activity and this is probably due to the modification of the redox properties of V-O-Cr site in addition to the accelerating desorption of products. An addition of large amount of steam in the reactants improved the yield of desired products. Both Lewis and Bronsted acid sites were detected on the surface of CrV0.95P0.05O4, and the number of the latter increased by the addition of steam. The enhanced activity by the addition of steam is interpreted by the fact that Bronsted acid sites are produced by the hydrolysis of V-O-Cr bond on the surface and activate picoline molecules by withdrawing the electrons of the pyridine ring, and at the same time, enable to accelerate the desorption of the acid products. Even in the absence of gaseous oxygen, the oxygenated products were formed, thus, a Mars and van Krevelen mechanism was suggested.
机译:已经通过“软化学”技术制备了一系列Cr-V混合氧化物催化剂(CrVO4,Cr_(1-x)Al_xVO4和CrV_(1-x)P_xO4)。通过混合原料的水溶液并控制pH值,制得纯钒酸钒结晶形式的钒酸铬(CrVO4-I和HI)。为了研究钒酸铬的催化与结构之间的关系,将制备的钒酸铬用于2-,3-和4-甲基吡啶的气相氧化中。 CrVO4-I(单斜晶)显示出比CrVO4-III(斜方晶)高得多的活性,表明V-O-Cr键中的桥连氧是催化活性的原因。在不改变CrVO4-I型结构的情况下,用Al或P代替一部分Cr或V的活性。通过在CrVO4-I中用Al替代Cr和用P替代V来提高酸度,从而加速产物的解吸。用P部分取代V可以显着提高活性,这可能是由于V-O-Cr位点的氧化还原特性得到了改善,同时产物的脱附加速了。在反应物中添加大量的蒸汽提高了所需产物的产率。在CrV0.95P0.05O4的表面上均检测到Lewis和Bronsted酸性位点,并且通过添加蒸汽增加了后者的数量。通过添加蒸汽来增强活性的解释是,布朗斯台德酸位是通过表面上的VO-Cr键的水解产生的,并通过吸收吡啶环的电子来激活甲基吡啶分子,同时使加速酸性产物的解吸。即使在没有气态氧气的情况下,也会形成氧化产物,因此提出了Mars and van Krevelen机制。

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