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Para-xylene adsorption separation process using nano-zeolite Ba-X

机译:纳米沸石Ba-X吸附对二甲苯的分离工艺

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The liquid phase adsorption process was studied on nano-zeolite Ba-X for separating para-xylene from a feed mixture containing all C8 aromatics. Nano-zeolite Ba-X with different ratios of SiO2/Al2O3 was synthesized through hydrothermal process and ion-exchanged with barium. The product was characterized by X-ray diffraction, scanning electron microscopy (SEM), nitrogen adsorption and in situ Fourier transform infrared (FTIR) spectroscopy. The adsorption process was carried out in a breakthrough system at temperature range of 120-160 °C under 4-7 atm pressure. The influence of nano-zeolite water content on the separation process was studied. The optimization of adsorption process was also investigated by changing the operation conditions. The adsorption isotherm for all C8 aromatic isomers and also desorbents indicated the typical Langmuir type. The selectivity factor of adsorbent for para-xylene and the adsorption capacity at saturation of the different adsorbate samples with each component from C8 aromatic mixture were determined. It was observed that the selectivity of para-xylene increased by barium ion-exchange of cationic sites in nano-zeolite X and the adsorbent selectivity for para-xylene relative to each of meta-xylene, ortho-xylene and ethyl-benzene under the optimum conditions was found to be 7.191, 2.819 and 3.745, in the order given. It was also studied the influence of desorbent type on its selectivity for para-xylene compared to each isomer from the C8 aromatic mixture.
机译:在纳米沸石Ba-X上研究了液相吸附过程,以从含有所有C8芳烃的进料混合物中分离对二甲苯。通过水热法合成了不同SiO2 / Al2O3比的纳米沸石Ba-X,并与钡进行了离子交换。通过X射线衍射,扫描电子显微镜(SEM),氮吸附和原位傅里叶变换红外(FTIR)光谱对产物进行表征。吸附过程是在突破系统中于4-7大气压下在120-160°C的温度范围内进行的。研究了纳米沸石含水量对分离过程的影响。通过改变操作条件对吸附过程的优化进行了研究。所有C8芳族异构体的吸附等温线以及解吸剂均显示了典型的Langmuir类型。确定了对二甲苯的吸附剂的选择性因子和不同吸附物样品中C8芳烃混合物中每种组分的饱和吸附容量。观察到在最佳条件下,相对于间二甲苯,邻二甲苯和乙基苯,纳米沸石X中阳离子位的钡离子交换和对二甲苯的吸附选择性相对于间二甲苯,邻二甲苯和乙苯均提高了对二甲苯的选择性。根据给定的顺序,发现条件为7.191、2.819和3.745。还研究了与C8芳香族混合物中每种异构体相比,解吸剂类型对其对二甲苯选择性的影响。

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