Spherical crosslinked polystyrene-isocyanuric acid resin was synthesized by reaction of chloromethylated polystyrene with isocyanuric acid. The sorption isotherms of phenol from aqueous solution and cyclohexane soluti...Spherical crosslinked polystyrene-isocyanuric acid resin was synthesized by reaction of chloromethylated polystyrene with isocyanuric acid. The sorption isotherms of phenol from aqueous solution and cyclohexane solution onto the resin were measured. It is of interest to notice that the resin sorbed phenol efficiently though its specific surface area was 0 and did not swell in water, and the sorption capacity.from aqueous solution was close to that of phenol onto XAD-4 at the same equilibrium concentration. Sorption enthalpies calculated from the isotherms according to the Clausius-Clapeyron equation were -2I~ -25lJ/mol and -39~ -41kJ/mol respectively. These values implied that the sorption processes were based on hydrogen bonding. In addition the details of the hydrogen bonding between the active sites of the resin and phenol were suggested.展开更多
The adsorption of two phenols, namely, phenol and salicylic acid(SA) onto a water-compatible hypercrosslinked polymeric resin(NJ-8) were studied in terms of pseudo-second-order and first order mechanisms for chemical ...The adsorption of two phenols, namely, phenol and salicylic acid(SA) onto a water-compatible hypercrosslinked polymeric resin(NJ-8) were studied in terms of pseudo-second-order and first order mechanisms for chemical sorption as well as an intraparticle diffusion mechanism process. Kinetic analysis showed that the intraparticle diffusion process was the essential rate-controlling step. The activation energies of sorption have also been evaluated with the pseudo-second-order and intraparticle diffusion constants, respectively. Adsorption equilibrium data were well fitted by the Langmuir, Freundlich and Redlich-Peterson isotherms. Adsorption was exothermic and basically of a type of transition between physical and chemical character. The sorption capacity was higher for SA due to its more hydrophobic. Phenol has a higher adsorption enthalpy since it could form stronger hydrogen bonding on NJ-8.展开更多
基金Supported by the National Natural Science Foundation of China !(Grant No. 29574164 and 29974015)
文摘Spherical crosslinked polystyrene-isocyanuric acid resin was synthesized by reaction of chloromethylated polystyrene with isocyanuric acid. The sorption isotherms of phenol from aqueous solution and cyclohexane solution onto the resin were measured. It is of interest to notice that the resin sorbed phenol efficiently though its specific surface area was 0 and did not swell in water, and the sorption capacity.from aqueous solution was close to that of phenol onto XAD-4 at the same equilibrium concentration. Sorption enthalpies calculated from the isotherms according to the Clausius-Clapeyron equation were -2I~ -25lJ/mol and -39~ -41kJ/mol respectively. These values implied that the sorption processes were based on hydrogen bonding. In addition the details of the hydrogen bonding between the active sites of the resin and phenol were suggested.
文摘The adsorption of two phenols, namely, phenol and salicylic acid(SA) onto a water-compatible hypercrosslinked polymeric resin(NJ-8) were studied in terms of pseudo-second-order and first order mechanisms for chemical sorption as well as an intraparticle diffusion mechanism process. Kinetic analysis showed that the intraparticle diffusion process was the essential rate-controlling step. The activation energies of sorption have also been evaluated with the pseudo-second-order and intraparticle diffusion constants, respectively. Adsorption equilibrium data were well fitted by the Langmuir, Freundlich and Redlich-Peterson isotherms. Adsorption was exothermic and basically of a type of transition between physical and chemical character. The sorption capacity was higher for SA due to its more hydrophobic. Phenol has a higher adsorption enthalpy since it could form stronger hydrogen bonding on NJ-8.
