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TGA–FTIR study of the thermal and SBA-15-catalytic pyrolysis of potassium citrate under nitrogen and air atmospheres

机译:TGa-FTIR研究在氮气和空气气氛下热和sBa-15催化热解柠檬酸钾

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摘要

In this work, the thermal and SBA-15 catalytic pyrolysis of potassium citrate has been studied by TGA/FTIR. According to the TGA results, in the absence of a catalyst, a decomposition mechanism based on a sequence of four consecutive reactions is proposed, yielding a solid residue plus potassium carbonate, which at temperatures of 650 °C evolves towards the formation of microporous activated carbons. The reaction scheme in an air atmosphere is quite similar, with the only exception of additional oxidation steps. As a general rule, the presence of SBA-15 as a catalyst seems to reduce the number of decomposition steps and to inhibit the last stages of the formation of porous carbons. The proposed mechanisms are in good agreement with the FTIR analysis of the evolution of the gases evolved at each temperature, as well as with the endothermic or exothermic character of the heat flow involved. A different way to interpret and compare the FTIR intensity data is proposed, which is complementary to the usual analysis based on the normalization with respect to the total amount of sample and permits us to more clearly interpret the role of the catalyst at each temperature. This type of analysis shows that the catalyst actually decreases the yields of volatile compounds obtained at each temperature, and enhances the true effect of the catalyst on the composition of the gases evolved at each temperature.
机译:在这项工作中,通过TGA / FTIR研究了柠檬酸钾的热和SBA-15催化热解。根据TGA结果,在不存在催化剂的情况下,提出了一种基于四个连续反应序列的分解机制,得到固体残余物加上碳酸钾,在650℃的温度下发展朝向形成微孔活化碳的形成。空气气氛中的反应方案非常相似,额外的氧化步骤唯一的例外。作为一般规则,作为催化剂的SBA-15存在似乎减少了分解步骤的数量,并抑制了多孔碳的形成的最后阶段。拟议的机制与在每个温度下进化的气体的进化的FTIR分析良好,以及所涉及的热流的吸热或放热特征。提出了一种解释和比较FTIR强度数据的不同方式,这与常规分析相对于关于样品总量的标准化,并且允许我们更清楚地解释每个温度下催化剂的作用。这种类型的分析表明,催化剂实际上降低了在每个温度下获得的挥发性化合物的产率,并增强了催化剂对在每个温度下进化的气体组合物上的真实效果。

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