Journal
ACS OMEGA
Volume 5, Issue 6, Pages 2575-2593Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.9b02842
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Funding
- Department of Science and Technology (DST) [DST/TM/WTI/2K15/121]
- Department of Science and Technology, New Delhi, India
- University Grant Commission (UGC), New Delhi
- Mississippi State University, USA [F.194-1/2014(IC)]
- Jawaharlal Nehru University [ID 189]
- DST PURSE, Government of India
- Advance Instrumentation Research Facility (AIRF) Jawaharlal Nehru University
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Rice and wheat husks were converted to biochars by slow pyrolysis (1 h) at 600 degrees C. Iron oxide rice husk hybrid biochar (RHIOB) and wheat husk hybrid biochar (WHIOB) were synthesized by copyrolysis of FeCl3-impregnated rice or wheat husks at 600 degrees C. These hybrid sorbents were characterized using X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy (SEM), SEM-energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, transmission electron microscopy, physical parameter measurement system, and Brunauer-Emmett-Teller (BET) surface area techniques. Fe3O4 was the predominant iron oxide present with some Fe3O4. RHIOB and WHIOB rapidly chemisorbed As(III) from water (similar to 24% removal in first half an hour reaching up to -100% removal in 24 h) at surface Fe-OH functions forming monodentate Fe-OAs(OH)(2) and bidentate ( Fe-O)(2)AsOH complexes. Optimum removal occurred in the pH 7.5-8.5 range for both RHIOB and WHIOB, but excellent removal occurred from pH 3 to 10. Batch kinetic studies at various initial adsorbate-adsorbent concentrations, temperatures, and contact times gave excellent pseudo-second-order model fits. Equilibrium data were fitted to different sorption isotherm models. Fits to isotherm models (based on R-2 and chi(2)) on RHIOB and WHIOB followed the order: Redlich-Peterson > Toth > Sips = Koble-Corrigan > Langmuir > Freundlich = Radke-Prausnitz > Temkin and Sips = Koble-Corrigan > Toth > Redlich-Peterson > Langmuir > Temkin > Freundlich = Radke-Prausnitz, respectively. Maximum adsorption capacities, Q(RHIOB)(0)= 96 mu g/g and Q(W)(HIOB)(0) = 111 mu g/g, were obtained. No As(III) oxidation to As(V) was detected. Arsenic adsorption was endothermic. Particle diffusion was a rate-determining step at low (<= 50 mu g/L) concentrations, but film diffusion controls the rate at >= 100-200 mu g/L. Binding interactions with RHIOB and WHIOB were established, and the mechanism was carefully discussed. RHIOB and WHIOB can successfully be used for As(III) removal in single and multicomponent systems with no significant decrease in adsorption capacity in the presence of interfering ions mainly Cl- , HCO3- , NO3- , SO4(2)(-), PO43-, K+, Na+, Ca2+. Simultaneous As(III) desorption and regeneration of RHIOB and WHIOB was successfully achieved. A very nominal decrease in As(III) removal capacity in four consecutive cycles demonstrates the reusability of RHIOB and WHIOB. Furthermore, these sustainable composites had good sorption efficiencies and may be removed magnetically to avoid slow filtration.
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