RESUMEN
Zeolite nanoparticles were synthesized by means of a hydrothermal method and the sorption performances were tested in batch experiments using single and binary components of Pb2+, Ni2+and Cu2+ synthetic solutions. Fast adsorption was observed and the majority of sorption occurred within the first 5 min for each case of metal cations. Percentage metal removal increased with the adsorbent dosage and it was adversely affected by the initial metal concentrations. XRD, FTIR-ATR and XPS analyses revealed that the removal of metal ions occurred mainly on the basis of ion-exchange. Equilibrium sorption data were best described by Sips isotherm model and the maximum attainable metal amount on the NaX were estimated as 1.23, 1.76 and 2.20 mmol/g for the Pb2+, Ni2+, and Cu2+ cations, respectively. A single step desorption process conducted in NaCl solution seemed to be practically applicable for regeneration and after three adsorption/desorption cycles, 79, 76 and 48% of initial sorption capacity of NaX were preserved for lead, nickel and copper ions, respectively. Single isotherm parameters used for the prediction of binary equilibrium data were satisfactory. Binary sorption experiments for Pb2+-Ni2+, Pb2+-Cu2+ and Ni2+-Cu2+ couples reflected that the presence of secondary ions decreased the uptake of the primary one. Lead exhibited greater inhibition of the sorption of nickel and copper, demonstrating the stronger affinity of NaX for Pb2+. Extended Freundlich model best described all the three binary metal systems. Adsorption experiments carried out in real wastewater demonstrated that NaX nanoparticle has a high affinity for all the cations except copper.
RESUMEN
Membrane adsorbers are promising candidates for the efficient and effective removal of heavy metals in waste water due to their unattainable adsorption and filtration capabilities. In the present study, zeolite nanoparticles incorporated polysulfone (PSf10) membrane was synthesized by means of non-solvent induced phase separation technique for the removal of lead and nickel ions in water. PSf10 showed a remarkable sorption capability and after repeated (adsorption/desorption)5 cycles in batch experiments, it preserved 77% and 92% of its initial sorption capacity for the lead and nickel, respectively. Addition of nanoparticles increased the pore radius of the native PSf from 10 to 19nm, while bovine serum albumin rejection remained unchanged at 98%. Increments in the pore size and enhancement in hydrophilicity caused to increase hydraulic permeability of the native PSf from 23 to 57L/m2hbar. Cross-flow filtration studies revealed that the filtrate concentrations were inversely affected by the initial metal concentration and transmembrane pressure due to reaction limited region. Nonlinear rational regression model perfectly described the filtration behavior of the PSf10 within the experimental range and suggested that lower initial metal concentration and pressure with a short filtration time should be selected for the target response to be minimum.
RESUMEN
In this study, the adsorption and the filtration processes were coupled by a zeolite nanoparticle impregnated polysulfone (PSf) membrane which was used to remove the lead and the nickel cations from synthetically prepared solutions. The results obtained from X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) analysis indicated that the synthesized zeolite nanoparticles, using conventional hydrothermal method, produced a pure NaX with ultrafine and uniform particles. The performance of the hybrid membrane was determined under dynamic conditions. The results also revealed that the sorption capacity as well as the water hydraulic permeability of the membranes could both be improved by simply tuning the membrane fabricating conditions such as evaporation period of the casting film and NaX loading. The maximum sorption capacity of the hybrid membrane for the lead and nickel ions was measured as 682 and 122 mg/g respectively at the end of 60 min of filtration, under 1 bar of transmembrane pressure. The coupling process suggested that the membrane architecture could be efficiently used for treating metal solutions with low concentrations and transmembrane pressures.