Singh Prachi, Sarswat Ankur, Pittman Charles U, Mlsna Todd, Mohan Dinesh
School of Environmental Sciences, Jawaharlal Nehru University, New Delhi 110067, India.
Department of Chemistry, Mississippi State University, Starkville, Mississippi State 39762, United States.
ACS Omega. 2020 Feb 6;5(6):2575-2593. doi: 10.1021/acsomega.9b02842. eCollection 2020 Feb 18.
Rice and wheat husks were converted to biochars by slow pyrolysis (1 h) at 600 °C. Iron oxide rice husk hybrid biochar (RHIOB) and wheat husk hybrid biochar (WHIOB) were synthesized by copyrolysis of FeCl-impregnated rice or wheat husks at 600 °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. FeO was the predominant iron oxide present with some FeO. RHIOB and WHIOB rapidly chemisorbed As(III) from water (∼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) and bidentate (≡Fe-O)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 and χ) 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, = 96 μg/g and = 111 μg/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 μg/L) concentrations, but film diffusion controls the rate at ≥100-200 μg/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, HCO , NO , SO , PO , K, Na, Ca. 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.
稻壳和麦壳通过在600℃下缓慢热解(1小时)转化为生物炭。通过在600℃下对浸渍FeCl的稻壳或麦壳进行共热解,合成了氧化铁稻壳混合生物炭(RHIOB)和麦壳混合生物炭(WHIOB)。使用X射线光电子能谱、X射线衍射、扫描电子显微镜(SEM)、SEM能量色散X射线光谱、傅里叶变换红外光谱、透射电子显微镜、物理参数测量系统和布鲁诺尔-埃米特-泰勒(BET)表面积技术对这些混合吸附剂进行了表征。FeO是存在的主要氧化铁,还有一些Fe₂O₃。RHIOB和WHIOB在表面Fe-OH官能团处迅速从水中化学吸附As(III)(前半小时去除率约为24%,24小时内达到约100%的去除率),形成单齿≡Fe-OAs(OH)和双齿(≡Fe-O)AsOH配合物。RHIOB和WHIOB在pH 7.5 - 8.5范围内实现最佳去除,但在pH 3至10范围内也有出色的去除效果。在不同的初始吸附质-吸附剂浓度、温度和接触时间下进行的批次动力学研究与伪二级模型拟合良好。平衡数据拟合到不同的吸附等温线模型。RHIOB和WHIOB对等温线模型(基于 和χ)的拟合顺序分别为:Redlich-Peterson > Toth > Sips = Koble-Corrigan > Langmuir > Freundlich = Radke-Prausnitz > Temkin和Sips = Koble-Corrigan > Toth > Redlich-Peterson > Langmuir > Temkin > Freundlich = Radke-Prausnitz。获得了最大吸附容量, = 96 μg/g和 = 111 μg/g。未检测到As(III)氧化为As(V)。砷吸附是吸热的。在低(≤50 μg/L)浓度下,颗粒扩散是速率决定步骤,但在≥100 - 200 μg/L时,膜扩散控制速率。建立了与RHIOB和WHIOB的结合相互作用,并仔细讨论了其机制。RHIOB和WHIOB可成功用于单组分和多组分系统中As(III) 的去除,在主要为Cl、HCO 、NO 、SO 、PO 、K、Na、Ca的干扰离子存在下,吸附容量无显著降低。成功实现了RHIOB和WHIOB的As(III)同时解吸和再生。在四个连续循环中,As(III)去除能力的非常小的下降证明了RHIOB和WHIOB的可重复使用性。此外,这些可持续复合材料具有良好的吸附效率,并且可以通过磁性去除以避免缓慢过滤。