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Homogeneous Redox Catalysts Based on Heteropoly Acid Solutions: I. Pilot Testing of a Catalyst and Methyl Ethyl Ketone Synthesis

机译:基于杂多酸溶液的均相氧化还原催化剂:I.催化剂和甲基乙基酮合成的中试

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The pilot experiments on methyl ethyl ketone (MEK) synthesis in 2005-2006 were aimed at developing a technology for highly selective n-butylene oxidation with oxygen into MEK in the presence of a new homogeneous catalyst. This catalyst was a chloride-free aqueous solution of Pd(II) + HPA-7', where HPA-7' is a vanadium-rich molybdovanadophosphoric acid of modified (non-Keggin) composition with the empirical formula H_(12)P_3Mo_(18)V_7O_(85). For ensuring the explosion and fire safety of the pilot unit, the MEK synthesis process was carried out in two steps conducted in different reactors. The catalyst solution in the pilot plant circulated in a closed loop. The target reaction (step (1)) was performed at 60°C and an n-butylene pressure of 9 bar in a tubular plug-flow reactor 1 in the absence of O_2. The high oxidation potential of the HPA-7' solution ensured a high rate of the reaction, which lasted <20 min. The separation of MEK from the reduced catalyst was carried out in a film evaporator (stripping column) at 100°C. Subsequent catalyst regeneration with atmospheric oxygen (step (2)) was performed in an original perfect-mixing reactor 2. At 160-190°C and a pressure of 20 bar (P_(O_2) = 4 bar), this step lasted 40-50 min. The regenerated catalyst was returned into reactor 1 to be involved in the next catalytic cycle. Thus, the catalytic oxidation of n-butylene with oxygen in the pilot plant was carried out in two steps, while MEK was drawn off continuously. The pilot tests demonstrated that the unsteady-state catalysis mode is appropriate for the two-step MEK synthesis. The Pd(II) + HPA-7' catalyst developed has a near-optimum composition. An analysis of the drawbacks of the pilot plant design showed the ways of attaining the rated production capacity, 250 (kg MEK)/day. The results of carrying out the MEK synthesis process on the pilot scale will be taken into consideration in developing two-step technologies for the oxidation of other organic compounds with oxygen in the presence of an HPA solution.
机译:在2005-2006年间进行的甲基乙基酮(MEK)合成的中试实验旨在开发一种在新的均相催化剂存在下,用氧气将氧选择性氧化成MEK的高选择性技术。该催化剂是Pd(II)+ HPA-7'的无氯化物水溶液,其中HPA-7'是改性钒组成的富含钒的钼钒钼酸,其经验式为H_(12)P_3Mo_( 18)V_7O_(85)。为了确保中试装置的爆炸和火灾安全,MEK合成过程分两步在不同的反应堆中进行。中试装置中的催化剂溶液在闭环中循环。目标反应(步骤(1))在不存在O_2的情况下,在管式活塞流反应器1中于60℃,正丁烯压力为9bar的条件下进行。 HPA-7'溶液的高氧化电位确保了高的反应速率,持续了不到20分钟。在膜蒸发器(汽提塔)中于100℃进行MEK与还原催化剂的分离。随后在原始的完美混合反应器2中用大气氧进行催化剂再生(步骤(2))。在160-190℃和20 bar的压力(P_(O_2)= 4 bar)下,该步骤持续40- 50分钟再生的催化剂返回到反应器1以参与下一个催化循环。因此,在中试装置中用氧气催化氧化正丁烯分两步进行,同时连续排出MEK。中试测试表明,非稳态催化模式适用于两步MEK合成。开发的Pd(II)+ HPA-7'催化剂的组成接近最佳。对中试工厂设计的弊端进行分析后,得出了达到250(kg MEK)/天的额定生产能力的方法。在开发在HPA溶液存在下用氧气氧化其他有机化合物的两步技术时,将考虑在中试规模上进行MEK合成过程的结果。

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