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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Selective Adsorption of C-6, C-8, and C-10 Linear alpha-Olefins from Binary Liquid-Phase Olefin/Paraffin Mixtures Using Zeolite Adsorbents: Experiment and Simulations
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Selective Adsorption of C-6, C-8, and C-10 Linear alpha-Olefins from Binary Liquid-Phase Olefin/Paraffin Mixtures Using Zeolite Adsorbents: Experiment and Simulations

机译:使用沸石吸附剂的二元液相烯烃/石蜡混合物选择性吸附C-6,C-8和C-10线性α-烯烃:实验和模拟

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摘要

The adsorption separation of gaseous olefin/paraffin using porous materials has been extensively studied from both experimental and molecular simulation perspectives, while the adsorption separation of liquid-phase olefin/paraffin has been much less studied. One of the most important reasons for this is that it is difficult to measure the actual adsorption capacity of liquid-phase adsorption separation directly through experiments, and the simulation results of most studies are compared to gas-phase measurements. In this paper, the selective adsorption of linear alpha-olefins from three binary liquid-phase olefin/paraffin mixtures, 1-hexene/n-hexane (C-6), 1-octene/n-octane (C-8), and 1-decene/n-decane (C-10), by zeolite adsorbents was systematically investigated using batch adsorption experiments and configurational-bias grand canonical Monte Carlo (CB-GCMC) simulations. In the batch experiments, based on the liquid-phase measurement method of the actual adsorption capacity that we developed, a modified commercial SA zeolite with a relatively large pore volume and surface area was used for adsorption. The results showed that the modified SA zeolite had larger actual adsorption capacities for C-6 and C-8 linear alpha-olefins, which increased by 51% and 56%, respectively, than the standard SA zeolite that was used in our previous work. The adsorption isotherms of C-6, C-8, and C-10 in the SA and 13X zeolites were calculated by CB-GCMC simulations. The visualized results of density profiles showed that the olefin molecules were densely distributed at the edge of the zeolite cages and that there were cases where a single molecule was adsorbed over two adjacent cages. The good agreement between the experimental and simulated data proves the completeness of the liquid-phase measurement method that we developed and the reliability of the simulation prediction.
机译:的吸附分离气态烯烃/链烷烃采用多孔材料已经被广泛地从实验和分子模拟研究的观点,而液体相的吸附分离烯烃/链烷烃已被少得多的影响。一个用于此的最重要原因是,它是难以直接通过实验来测量液相吸附分离的实际吸附能力,和大多数研究的模拟结果进行比较,以气相的测量。在本文中,直链α-烯烃的选择性吸附从三个二进制液相烯烃/链烷烃的混合物,1-己烯/正 - 己烷(C-6),1-辛烯/正辛烷(C-8),和1-癸烯/正癸烷(C-10),由沸石吸附剂是使用分批吸附实验和构型偏压的蒙特卡罗(CB-GCMC)模拟系统地研究。在间歇实验中,基于实际的吸附能力,我们开发的液相测定方法中,用于吸附具有相对大的孔体积和表面积的改性商业SA沸石。结果表明,所述改性SA沸石具有更大的实际吸附量为C-6和C-8直链α-烯烃,其分别增加51%和56%,比在我们以前的工作中使用的标准SA沸石。 C-6,C-8和C-10中的SA和13X沸石的吸附等温线,通过CB-GCMC模拟计算。的密度分布的可视化结果表明,烯烃分子密集分布在沸石笼的边缘,并且有在一个单一的分子被吸附在两个相邻的保持架的情况。所述实验和模拟数据之间的良好的一致性证明液相测定方法,我们开发和模拟预测的可靠性的完整性。

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