1,3 丙二醇 + 二甲亚砜二元体系中稀释二氧化硫的吸收、解吸和机理研究

IF 1.4 4区 化学 Q4 CHEMISTRY, PHYSICAL
Huifang Guo, Ying Zhang, Qiaomin Zhang, Jia Liu, Xiaohong Xie
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引用次数: 0

摘要

这项研究利用 1,3-丙二醇 (PDO) + 二甲基亚砜 (DMSO) 体系研究了二氧化硫 (SO2) 的吸收,并分析了压力为 123.15 kPa、温度范围为 298.15-318.15 K(温度梯度为 5 K)的气液平衡 (GLE) 数据。通过拟合气液平衡数据,可以发现二氧化硫的吸收过程符合亨利定律。同时还计算了二氧化硫吸收过程中的比熵、比焓和吉布斯自由能的变化。此外,还研究了 PDO + DMSO 系统在常压下的捕获和再生特性,再生实验结果表明,通过加热和用 N2 鼓泡,97.3% 的 SO2 可以被解吸。此外,经过多次循环后,吸收溶剂的吸收能力没有明显下降。最后,利用傅立叶变换红外光谱和计算信息分析了二氧化硫与系统之间的相互作用。因此,可以推断出 PDO、DMSO 和 SO2 之间存在分子间氢键联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Absorption, Desorption, and Mechanism Investigation of Dilute SO2 in the 1,3-Propanediol + Dimethyl Sulfoxide Binary System

Absorption, Desorption, and Mechanism Investigation of Dilute SO2 in the 1,3-Propanediol + Dimethyl Sulfoxide Binary System

In this work, the absorption of sulfur dioxide (SO2) was investigated using the 1,3-propanediol (PDO) + dimethyl sulfoxide (DMSO) system, and the gas−liquid equilibrium (GLE) data were analyzed over a temperature range of 298.15–318.15 K (with a temperature gradient of 5 K) at a pressure of 123.15 kPa. By fitting the gas–liquid equilibrium data, it is observed that the process of absorption SO2 conforms to Henry’s Law. The change in specific entropy, enthalpy, and Gibbs free energies of the SO2 absorption process was as well calculated. In addition, the capture and regeneration properties of the PDO + DMSO system were investigated under atmospheric pressure, and the results of regeneration experiments demonstrated that 97.3% of SO2 could be desorbed by heating and bubbling with N2. Furthermore, there was no notable reduction in absorption capacity of the absorbent solvents after multiple cycles. Finally, the FTIR spectra and computational information were noted to analyze the interaction between SO2 and the system. As a result, an intermolecular hydrogen bonding association between PDO, DMSO, and SO2 can be inferred.

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来源期刊
Journal of Solution Chemistry
Journal of Solution Chemistry 化学-物理化学
CiteScore
2.30
自引率
0.00%
发文量
87
审稿时长
3-8 weeks
期刊介绍: Journal of Solution Chemistry offers a forum for research on the physical chemistry of liquid solutions in such fields as physical chemistry, chemical physics, molecular biology, statistical mechanics, biochemistry, and biophysics. The emphasis is on papers in which the solvent plays a dominant rather than incidental role. Featured topics include experimental investigations of the dielectric, spectroscopic, thermodynamic, transport, or relaxation properties of both electrolytes and nonelectrolytes in liquid solutions.
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