Modeling of H(2)S solubility in ionic liquids: comparison of white-box machine learning, deep learning and ensemble learning approaches

In the context of gas processing and carbon sequestration, an adequate understanding of the solubility of acid gases in ionic liquids (ILs) under various thermodynamic circumstances is crucial. A poisonous, combustible, and acidic gas that can cause environmental damage is hydrogen sulfide (H(2)S). ILs are good choices for appropriate solvents in gas separation procedures. In this work, a variety of machine learning techniques, such as white-box machine learning, deep learning, and ensemble learning, were established to determine the solubility of H(2)S in ILs. The white-box models are group method of data handling (GMDH) and genetic programming (GP), the deep learning approach is deep belief network (DBN) and extreme gradient boosting (XGBoost) was selected as an ensemble approach. The models were established utilizing an extensive database with 1516 data points on the H(2)S solubility in 37 ILs throughout an extensive pressure and temperature range. Seven input variables, including temperature (T), pressure (P), two critical variables such as temperature (T(c)) and pressure (P(c)), acentric factor (ω), boiling temperature (T(b)), and molecular weight (Mw), were used in these models; the output was the solubility of H(2)S. The findings show that the XGBoost model, with statistical parameters such as an average absolute percent relative error (AAPRE) of 1.14%, root mean square error (RMSE) of 0.002, standard deviation (SD) of 0.01, and a determination coefficient (R(2)) of 0.99, provides more precise calculations for H(2)S solubility in ILs. The sensitivity assessment demonstrated that temperature and pressure had the highest negative and highest positive affect on the H(2)S solubility in ILs, respectively. The Taylor diagram, cumulative frequency plot, cross-plot, and error bar all demonstrated the high effectiveness, accuracy, and reality of the XGBoost approach for predicting the H(2)S solubility in various ILs. The leverage analysis shows that the majority of the data points are experimentally reliable and just a small number of data points are found beyond the application domain of the XGBoost paradigm. Beyond these statistical results, some chemical structure effects were evaluated. First, it was shown that the lengthening of the cation alkyl chain enhances the H(2)S solubility in ILs. As another chemical structure effect, it was shown that higher fluorine content in anion leads to higher solubility in ILs. These phenomena were confirmed by experimental data and the model results. Connecting solubility data to the chemical structure of ILs, the results of this study can further assist to find appropriate ILs for specialized processes (based on the process conditions) as solvents for H(2)S.