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首页> 外文期刊>Journal of the American Oil Chemists' Society >Liquid Phase Selective Catalytic Oxidation of Oleic Acid to Azelaic Acid Using Air and Transition Metal Acetate Bromide Complex
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Liquid Phase Selective Catalytic Oxidation of Oleic Acid to Azelaic Acid Using Air and Transition Metal Acetate Bromide Complex

机译:使用空气和过渡金属醋酸盐溴络合物液相选择性催化催化氧化油酸与壬二酸

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Industrially important di-carboxylic acids are synthesized from mono-carboxylic unsaturated and unsaturated fatty acids. In this study, the aim is to perform the simultaneous catalytic oxidative C=C cleavage of oleic acid (OA) to azelaic acid and pelargonic acid, and oxidation of the terminal methyl group in pelargonic acid to azelaic acid using cobalt- and manganese-acetate as catalyst, hydrogen bromide as co-catalyst and air in acetic acid at elevated pressure (2.8-5.8 barg) and temperature (353-383 K). Oxygen solubility is determined under varying pressure, temperature and OA loading. The effect of OA loading, pressure and temperature on OA conversion and azelaic acid selectivity is studied by varying one variable at a time; however, the presence of the synergistic effect of the catalyst and co-catalyst is investigated by central composite design assisted response surface methodology. Oxidation of terminal methyl group in saturated fatty acid is also confirmed by the oxidation of stearic acid to octadecanedioic acid using identical oxidation conditions of OA. Oxidation products of fatty acids are quantified by gas chromatographic analysis. The innovation of the work is thus the ability of the catalytic system to perform a total oxidation of a terminal methyl group of the hydrocarbon chain. OA oxidation kinetics relating to catalyst and co-catalyst concentration along with oxygen solubility at elevated temperature and pressure is established. The frequency factor and activation energy for OA oxidation is determined using the Arrhenius equation.
机译:工业上重要的二羧酸由单羧酸不饱和和不饱和脂肪酸合成。在本研究中,目的是使用钴和乙酸钴和乙酸锰对偶酸(OA)的同时催化氧化C = C切割油酸(OA)与偶氮酸和藻酸,对偶氮酸的末端甲基氧化作为催化剂,溴化氢作为乙酸的助催化剂和空气,升高的压力(2.8-5.8副)和温度(353-383k)。在不同的压力,温度和OA负载下测定氧溶解度。通过在一次改变一个变量,研究了OA加载,压力和温度对OA转化和偶氮酸选择性的影响;然而,通过中央复合设计辅助响应面方法研究了催化剂和助催化剂协同作用的存在。使用相同的OA的相同氧化条件,还通过氧化酸至十八烷基二酸的氧化剂氧化末端甲基在饱和脂肪酸中的氧化。通过气相色谱分析量化脂肪酸的氧化产物。因此,作品的创新是催化系统对烃链的总甲基进行总氧化的能力。建立了与催化剂和助催化剂浓度相关的氧化动力学以及在升高的温度和压力下的氧溶解度。使用Arrhenius方程确定OA氧化的频率因数和激活能。

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