Zhe Yang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Zhe Yang has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Bo Liu
School of Mathematics and Physics, Xi’an Jiaotong-Liverpool University, Suzhou 215123, China
3 shared publications - Huijie Zhu
Henan International Joint Laboratory of New Civil Engineering Structure, School of Intelligent Construction and Civil Engineering, Luoyang Institute of Science and Technology, Luoyang 471023, China
3 shared publications - Jianhong Lu
North China University of Water Resources and Electric Power, School of Ecology and Environment, Zhengzhou, China
3 shared publications - Mingyan Shi
College of Civil Engineering, Guangzhou University, Guangzhou 510006, China
3 shared publications - Qiang Huang
Henan International Joint Laboratory of New Civil Engineering Structure, College of Civil Engineering, Luoyang Institute of Science and Technology, Luoyang 471023, China
3 shared publications - Shuai Fu
School of Intelligent Construction and Civil Engineering, Intelligent Water Research Institute, Luoyang Institute of Technology, Luoyang 471000, China
3 shared publications
Latest Publications
- Open Access
Accumulation of Vanadium by Nanoscale Zero-Valent Iron Supported by Activated Carbon under Simulation Water Conditions: A Batch Study
Vanadium (V(V)) removal from simulation water (SW) was successfully accomplished using nanoscale zero-valent iron that was immobilized by activated carbon (NZVI/AC) which was used as an adsorbent. We investigated the effects of different parameters on V(V) removal, such as pH, dissolved oxygen (DO), common ions and adsorption kinetics for SW. The intraparticle diffusion model fits this study well (R2 > 0.9) according to the results of the kinetics investigation which showed that the adsorption of vanadium by NZVI/AC was rapid in the first 12 h and that equilibrium was reached in about 72 h. The amount of V(V) that was removed from the solution increased when it was subjected to pH 2 to pH 8, and this decreased after pH 8. While the effects of other anions and humic acid were negligible, the elimination of V(V) was significantly reduced by using phosphate and silicate. Fe2+ and Al3+, two common metal cations, improved the V(V) adsorption. High oxygen levels impeded the vanadium elimination, while anoxic conditions encouraged it. Elution with 0.1 M NaOH can be used to renew NZVI/AC in an efficient manner.
Open AccessAccumulation of Vanadium by Nanoscale Zero-Valent Iron Supported by Activated Carbon under Simulation Water Conditions: A Batch Study
Vanadium (V(V)) removal from simulation water (SW) was successfully accomplished using nanoscale zero-valent iron that was immobilized by activated carbon (NZVI/AC) which was used as an adsorbent. We investigated the effects of different parameters on V(V) removal, such as pH, dissolved oxygen (DO), common ions and adsorption kinetics for SW. The intraparticle diffusion model fits this study well (R2 > 0.9) according to the results of the kinetics investigation which showed that the adsorption of vanadium by NZVI/AC was rapid in the first 12 h and that equilibrium was reached in about 72 h. The amount of V(V) that was removed from the solution increased when it was subjected to pH 2 to pH 8, and this decreased after pH 8. While the effects of other anions and humic acid were negligible, the elimination of V(V) was significantly reduced by using phosphate and silicate. Fe2+ and Al3+, two common metal cations, improved the V(V) adsorption. High oxygen levels impeded the vanadium elimination, while anoxic conditions encouraged it. Elution with 0.1 M NaOH can be used to renew NZVI/AC in an efficient manner.
- Open Access
Removal of Antimony(V) from Drinking Water Using nZVI/AC: Optimization of Batch and Fix Bed Conditions
Antimony (Sb) traces in water pose a serious threat to human health due to their negative effects. In this work, nanoscale zero-valent iron (Fe0) supported on activated carbon (nZVI) was employed for eliminating Sb(V) from the drinking water. To better understand the overall process, the effects of several experimental variables, including pH, dissolved oxygen (DO), coexisting ions, and adsorption kinetics on the removal of Sb(V) from the SW were investigated by employing fixed-bed column runs or batch-adsorption methods. A pH of 4.5 and 72 h of equilibrium time were found to be the ideal conditions for drinking water. The presence of phosphate (), silicate (), chromate () and arsenate () significantly decreased the rate of Sb(V) removal, while humic acid and other anions exhibited a negligible effect. The capacity for Sb(V) uptake decreased from 6.665 to 2.433 mg when the flow rate was increased from 5 to 10 mL·min−1. The dynamic adsorption penetration curves of Sb(V) were 116.4% and 144.1% with the weak magnetic field (WMF) in fixed-bed column runs. Considering the removal rate of Sb(V), reusability, operability, no release of Sb(V) after being incorporated into the iron (hydr)oxides structure, it can be concluded that WMF coupled with ZVI would be an effective Sb(V) immobilization technology for drinking water.Open AccessRemoval of Antimony(V) from Drinking Water Using nZVI/AC: Optimization of Batch and Fix Bed Conditions
Antimony (Sb) traces in water pose a serious threat to human health due to their negative effects. In this work, nanoscale zero-valent iron (Fe0) supported on activated carbon (nZVI) was employed for eliminating Sb(V) from the drinking water. To better understand the overall process, the effects of several experimental variables, including pH, dissolved oxygen (DO), coexisting ions, and adsorption kinetics on the removal of Sb(V) from the SW were investigated by employing fixed-bed column runs or batch-adsorption methods. A pH of 4.5 and 72 h of equilibrium time were found to be the ideal conditions for drinking water. The presence of phosphate (), silicate (), chromate () and arsenate () significantly decreased the rate of Sb(V) removal, while humic acid and other anions exhibited a negligible effect. The capacity for Sb(V) uptake decreased from 6.665 to 2.433 mg when the flow rate was increased from 5 to 10 mL·min−1. The dynamic adsorption penetration curves of Sb(V) were 116.4% and 144.1% with the weak magnetic field (WMF) in fixed-bed column runs. Considering the removal rate of Sb(V), reusability, operability, no release of Sb(V) after being incorporated into the iron (hydr)oxides structure, it can be concluded that WMF coupled with ZVI would be an effective Sb(V) immobilization technology for drinking water. - Open Access
- 25 July 2021
- Published by MDPI AG in Nanomaterials
- Vol. 11 (8) , 1912
Adsorption of Sb(III) from Aqueous Solution by nZVI/AC: A Magnetic Fixed-Bed Column Study
The effectiveness of nanoscale zero-valent iron(nZVI) immobilized on activated carbon (nZVI/AC) in removing antimonite (Sb(III)) from simulated contaminated water was investigated with and without a magnetic fix-bed column reactor. The experiments were all conducted in fixed-bed columns. A weak magnetic field (WMF) was proposed to increase the exclusion of paramagnetic Sb(III) ions by nZVI/AC. The Sb(III) adsorption to the nZVI and AC surfaces, as well as the transformation of Sb(III) to Sb(V) by them, were both increased by using a WMF in nZVI/AC. The increased sequestration of Sb(III) by nZVI/AC in the presence of WMF was followed by faster nZVI corrosion and dissolution. Experiments were conducted as a function of the pH of the feed solution (pH 5.0–9.0), liquid flow rate (5–15 mL·min−1), starting Sb(III) concentration (0.5–1.5 mg·L−1), bed height nZVI/AC (10–40 cm), and starting Sb(III) concentration (0.5–1.5 mg·L−1). By analyzing the breakthrough curves generated by different flow rates, different pH values, different inlet Sb(III) concentrations, and different bed heights, the adsorbed amounts, equilibrium nZVI uptakes, and total Sb(III) removal percentage were calculated in relation to effluent volumes. At pH 5.0, the longest nZVI breakthrough time and maximal Sb(III) adsorption were achieved. The findings revealed that the column performed effectively at the lowest flow rate. With increasing bed height, column bed capacity and exhaustion time increased as well. Increasing the Sb(III) initial concentration from 0.5 to 1.5 mg·L−1 resulted in the rise of adsorption bed capacity from 3.45 to 6.33 mg·g−1.
- 25 July 2021
- Published by MDPI AG in Nanomaterials
- Vol. 11 (8) , 1912
Open AccessAdsorption of Sb(III) from Aqueous Solution by nZVI/AC: A Magnetic Fixed-Bed Column Study
The effectiveness of nanoscale zero-valent iron(nZVI) immobilized on activated carbon (nZVI/AC) in removing antimonite (Sb(III)) from simulated contaminated water was investigated with and without a magnetic fix-bed column reactor. The experiments were all conducted in fixed-bed columns. A weak magnetic field (WMF) was proposed to increase the exclusion of paramagnetic Sb(III) ions by nZVI/AC. The Sb(III) adsorption to the nZVI and AC surfaces, as well as the transformation of Sb(III) to Sb(V) by them, were both increased by using a WMF in nZVI/AC. The increased sequestration of Sb(III) by nZVI/AC in the presence of WMF was followed by faster nZVI corrosion and dissolution. Experiments were conducted as a function of the pH of the feed solution (pH 5.0–9.0), liquid flow rate (5–15 mL·min−1), starting Sb(III) concentration (0.5–1.5 mg·L−1), bed height nZVI/AC (10–40 cm), and starting Sb(III) concentration (0.5–1.5 mg·L−1). By analyzing the breakthrough curves generated by different flow rates, different pH values, different inlet Sb(III) concentrations, and different bed heights, the adsorbed amounts, equilibrium nZVI uptakes, and total Sb(III) removal percentage were calculated in relation to effluent volumes. At pH 5.0, the longest nZVI breakthrough time and maximal Sb(III) adsorption were achieved. The findings revealed that the column performed effectively at the lowest flow rate. With increasing bed height, column bed capacity and exhaustion time increased as well. Increasing the Sb(III) initial concentration from 0.5 to 1.5 mg·L−1 resulted in the rise of adsorption bed capacity from 3.45 to 6.33 mg·g−1.