Evaluation of kinetic salt-en ric hment behavior and separation performance of HFC-152a hydrate-based desalination using an experimental measurement and a thermodynamic correlation

Abstract

Hydrate-based desalination (HBD), a type of freezing-based desalination, can concentrate salts of saline water and produce fresh water via hydrate crystal formation. In this study, the thermodynamic stability, crystallographic information, and kinetic growth behavior of HFC-152a hydrate were investigated to estimate the desalination efficiency of HBD. The phase equilibria revealed that the HFC-152a hydrate could be formed at a higher temperature in the presence of NaCl (0 wt%, 3.5 wt%, and 8.0 wt%) than the HFC-134a hydrate at 0.3 MPa. The hydration number of the HFC-152a hydrate (sI) was found to be 7.74 through the Rietveld refinement of the powder X-ray diffraction patterns, and it was also used to determine the dissociation enthalpy of the HFC-152a hydrate. The Hu-Lee-Sum correlation was employed to predict the equilibrium shift and hydrate depression temperature of both HFC-152a and HFC-134a hydrates in the presence of NaCl. Faster hydrate growth kinetics and higher hydrate conversion were observed for the HFC-152a hydrate in saline solutions despite the smaller initial driving force at 0.3 MPa and the subcooling temperature of 3 K. Additionally, to quantify the desalination efficiency of the HFC-152a HBD, the maximum achievable salinity and maximum water yield were examined using the HLS correlation. The salt-enrichment efficiency decreased with an increase in the initial salinity and increased with increasing the subcooling. The overall results indicate that HFC-152a is, potentially, a superior candidate for HBD. The novel approach examined in this study will be useful for assessing the desalination efficiency of the HBD process. (c) 2021 Elsevier Ltd. All rights reserved.