用Wilson-NRF模型研究CO2在K2CO3水溶液中的溶解度

R. Moradi, S. Mazloumi
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引用次数: 0

摘要

与胺溶液相比,热碳酸钾(PC)溶液具有较低的再生能量和较高的化学溶解度。为了得到该体系的汽液方程(VLE)并预测其溶解度,本研究采用了离子特异性非电解质Wilson-NRF局部组成模型(isNWN);这个模型的框架是分子的。因此,它适用于电解质和非电解质溶液。本研究采用NWN模型和Pitzer-Debye-Huckel理论来评估电解液溶液在短期和长期的过量吉布斯能的贡献。在考虑温度范围和压力范围的情况下,模型中溶解度和水溶液体系的数据相互关联。()和()系统的平均绝对误差分别为和。实验结果及与其他模型的比较表明,该模型的实验数据是完全相关的。
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Investigating the Solubility of CO2 in the Solution of Aqueous K2CO3 Using Wilson-NRF Model
Hot potassium carbonate (PC) solution in comparison with amine solution had a decreased energy of regeneration and a high chemical solubility of . To present vapor and liquid equation (VLE) of this system and predict  solubility, the ion specific non-electrolyte Wilson-NRF local composition model (isNWN) was used in this study; the framework of this model was molecular. Therefore, it was suitable for both electrolyte and non-electrolyte solutions. The present research employed the NWN model and the Pitzer-Debye-Huckel theory in order to assess the contribution of the excess Gibbs energy of electrolyte solutions in a short and long range. The data of  solubility in water and the system of aqueous  were correlated in the model considering a temperature range of  and a pressure range of and . The average absolute error of ( ) and ( ) systems were  and  respectively. The results and comparisons with other models proved that the experimental data were exactly correlated in the model.
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