Forward osmosis with direct contact membrane distillation using tetrabutylphosphonium p-toluenesulfonate as an effective and safe thermo-recyclable osmotic agent for seawater desalination.
Chemosphere
; 263: 128070, 2021 Jan.
Article
em En
| MEDLINE
| ID: mdl-33297074
A phosphonium-based ionic liquid (IL) with lower critical solution temperature (LCST) property was assessed as a reusable draw solution (DS) for forward osmosis (FO). Tetrabutylphosphonium p-toluenesulfonate ([P4444]TsO) was successfully synthesized by neutralization reaction. Characterization results reveal its ability to generate sufficient osmotic pressure (14-68 bars for 0.5-2 M DS) to create a gradient across the FO membrane. Its thermal, physico-chemical and other colligative properties are favorable for its application as an osmotic agent. The LCST behavior of [P4444]TsO was found reversible and its phase separation from water can be done above its cloud point temperature Tc â¼57 °C. In vitro cytotoxicity tests from LDH and MTT assay reveal that it can be safely used as DS at an effective concentration EC30 â¼57 mg L-1 as its non-toxic level. Results from FO operations demonstrate that 2 M [P4444]TsO DS can effectively treat saline feed like seawater (0.6 M NaCl) with reasonable Jv = 1.35 ± 0.15 L m-2h-1, low Js = 0.0038 ± 0.00049 mol m-2h-1, and considerably low specific solute flux (Js/Jv â¼ 0.0028 mol L-1). After FO, â¼98% of [P4444]TsO was precipitated by heating the DS at 60 °C and conveniently reused with consistent FO performance. Direct contact membrane distillation (DCMD) was found effective in removing the residual 2% [P4444]TsO in the DS supernatant to finally produce high-quality effluent with concentrations way below the EC30 limit. Cost estimates for the entire process reveal the potential of FO combined with thermo-cyclic [P4444]TsO regeneration with DCMD for desalination application.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Destilação
/
Purificação da Água
Idioma:
En
Revista:
Chemosphere
Ano de publicação:
2021
Tipo de documento:
Article