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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Catalytic wet-air oxidation of aqueous solutions of formic acid, acetic acid and phenol in a continuous-flow trickle-bed reactor over Ru/TiO2 catalysts
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Catalytic wet-air oxidation of aqueous solutions of formic acid, acetic acid and phenol in a continuous-flow trickle-bed reactor over Ru/TiO2 catalysts

机译:Ru / TiO2催化剂上连续滴流床反应器中甲酸,乙酸和苯酚水溶液的催化湿空气氧化

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Catalytic wet-air oxidation of aqueous solutions of formic acid, acetic acid and phenol was carried out in a trickle-bed reactor at T= 328-523 K and total pressures up to 50 bar over various Ru/TiO2 catalysts. Complete oxidation of formic acid was obtained at mild operating conditions, and no catalyst deactivation occurred that could be attributed to the dissolution of active ingredient material. It was observed that besides oxidation route thermal decomposition contributes significantly to the removal of formic acid; Ru/TiO2 catalysts could be thus efficiently used for transformation of HCOOH to H2 and CO2 in an inert atmosphere. Liquid-phase oxidation of acetic acid was found to be structure sensitive; the highest catalyst activity was obtained, when Ru phase on the catalyst surface prevailed in zero-valent state. Due to simultaneous oxidation of metallic Ru to RuO2 during the reaction course, correspondingly lower conversion of acetic acid was measured in the reactor outlet. The employed Ru/TiO2 catalysts enable complete removal of phenol and TOC at temperatures above 483 K; at these conditions, no carbonaceous deposits were accumulated on the catalyst surface. Apparent catalyst deactivation observed at temperatures below 463 K is attributed to strong adsorption of partially oxidized intermediates on the catalyst surface, which can be avoided by conducting the CWAO process at sufficiently high temperatures. The acute toxicity to Daphnia magna and Vibrio fischeri of end-product solutions compared with that of the feed solutions was significantly reduced by oxidative treatment over Ru/TiO2 catalysts.
机译:在滴流床反应器中,在T = 328-523 K,总压力高达50 bar的各种Ru / TiO2催化剂上,进行甲酸,乙酸和苯酚水溶液的催化湿式空气氧化。在温和的操作条件下,甲酸被完全氧化,没有发生催化剂失活的现象,这可能归因于活性成分物质的溶解。观察到,除氧化途径外,热分解还显着促进了甲酸的去除。因此,Ru / TiO2催化剂可在惰性气氛下有效地用于将HCOOH转化为H2和CO2。乙酸的液相氧化被发现对结构敏感。当催化剂表面上的Ru相占零价状态时,可获得最高的催化剂活性。由于在反应过程中金属Ru同时氧化成RuO2,因此在反应器出口测得乙酸转化率较低。使用的Ru / TiO2催化剂能够在483 K以上的温度下完全去除苯酚和TOC;在这些条件下,在催化剂表面上没有积碳的沉积物。在低于463 K的温度下观察到的明显的催化剂失活归因于部分氧化的中间体在催化剂表面的强烈吸附,这可以通过在足够高的温度下进行CWAO工艺来避免。通过在Ru / TiO2催化剂上进行氧化处理,与进料溶液相比,最终产品溶液对水蚤和费氏弧菌的急性毒性大大降低。

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