Radiation induced in-situ cationic polymerization of polystyrene organogel for selective absorption of cholorophenols from petrochemical wastewater
Résumé
A new in-situ cationic polymerization was performed to synthesize a cross-linked (91%) polystyrene (PS) organogel through tetrachloroethylene radiolysis assisted by 60Co gamma rays. Hoernschemeyer diagram and swelling capacity test show a better selectivity of PS organogel to chlorinated molecules compared to ester, hydrocarbons and alcohols organic molecules by 80–184 folds. Response surface modeling (RSM) of CPs (2,4,6-trichlorophenol) sorption from artificial wastewater confirm superiority of PS organogel to absorb 1746 μmol CPs/g (∼345 mg CPs/g) at broad pH (4–10) and temperature (25–45 °C). Based on ANOVA statistic, simulated CPs absorption model onto PS organogel was successfully developed, with accuracy of prediction of R 2 ≈ R A d j 2 of 0.991–0.995 and lower coefficient of variation of 2.73% with F m o d e l of 611.4 at p < .0001. Particularly, the usage of PS organogel for petroleum wastewater reclamation exhibited higher absorption affinities for all the organic contaminants especially for CPs (>99%) by non-covalent and/or dispersive interaction mechanisms with a well-term reusability and good stability up to 5 cycles.