Enhancing sulfasalazine solubility in supercritical carbon dioxide with ethanol cosolvent: a comprehensive study.

利用乙醇作为助溶剂提高柳氮磺胺吡啶在超临界二氧化碳中的溶解度:一项综合研究。

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In this study, the solubility of sulfasalazine in supercritical carbon dioxide, using ethanol as a cosolvent, was evaluated at temperatures of 308, 318, 328, and 338 K, and at pressures reaching up to 30 MPa. A comprehensive examination was conducted to ascertain the impact of temperature, pressure, and cosolvent concentration on solubility and density. To this end, SRK as an equation of state and a range of semi-empirical correlations were employed to correlate the solubility. The Soltani-Mazloumi and Madras et al. models were identified as the most suitable model for the experimental data. The mole fraction of sulfasalazine ranged from 0.273 × 10(-4) to 1.654 × 10(-4) in the binary system, and from 1.535 × 10(-4) to 5.211 × 10(-4) and 3.263 × 10(-4) to 11.451 × 10(-4) at concentrations of 1 and 3 mol%, respectively. The findings indicated that the incorporation of a cosolvent, notably ethanol, led to a substantial enhancement in solubility. The sulfasalazine-ethanol-CO(2) system demonstrated the highest solubility at 12 MPa and 338 K, exhibiting approximately 11.95 times greater solubility compared to that observed in pure supercritical CO(2).

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