Rongshu Zhu
Harbin Institute of Technology
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Rongshu Zhu.
environmental science and information application technology | 2010
Fei Tian; Rongshu Zhu; Lingling Zhang; Weiqian Pan; Feng Ouyang; Wenyi Dong
The effects of various inorganic anions (SO<sub>4</sub><sup>2-</sup>, NO<sub>3</sub><sup>-</sup>, H<sub>2</sub>PO<sub>4</sub><sup>-</sup>, HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup>, F<sup>-</sup>, Cl<sup>-</sup>, Br<sup>-</sup> and I<sup>-</sup>) on the photocatalytic degradation of phenol were investigated under UV light irradiation. In present work, low initial pH value in the presence of H<sub>2</sub>PO<sub>4</sub><sup>-</sup> increased the photocatalytic degradation efficiency of TiO<sub>2</sub>, high initial pH value in the presence of HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup> and F<sup>-</sup> decreased the photocatalytic degradation efficiency of TiO<sub>2</sub>, and no change of initial pH value in the presence of SO<sub>4</sub><sup>2-</sup> and NO<sub>3</sub><sup>-</sup> had little effect on the photocatalytic degradation efficiency of TiO<sub>2</sub>. The results indicated that the effects of the inorganic anions on the photocatalytic degradation of phenol depended strongly on the pH, which was related with the adsorption of phenol on the surface of TiO<sub>2</sub>. No significant relationship between the initial pH and the photocatalytic degradation efficiency of TiO<sub>2</sub> was observed in the experiment with the addition of Cl<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup>, indicating that inorganic anions inhibited the photocatalytic degradation efficiency of TiO<sub>2</sub> by their trapping hydroxyl radicals (OH·).
environmental science and information application technology | 2010
Fei Tian; Rongshu Zhu; Lingling Zhang; Weiqian Pan; Feng Ouyang; Wenyi Dong
The effects of various inorganic anions (SO<sub>4</sub><sup>2-</sup>, NO<sub>3</sub><sup>-</sup>, H<sub>2</sub>PO<sub>4</sub><sup>-</sup>, HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup>, F<sup>-</sup>, Cl<sup>-</sup>, Br<sup>-</sup> and I<sup>-</sup>) on the photocatalytic degradation of phenol were investigated under UV light irradiation. In present work, low initial pH value in the presence of H<sub>2</sub>PO<sub>4</sub><sup>-</sup> increased the photocatalytic degradation efficiency of TiO<sub>2</sub>, high initial pH value in the presence of HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup> and F<sup>-</sup> decreased the photocatalytic degradation efficiency of TiO<sub>2</sub>, and no change of initial pH value in the presence of SO<sub>4</sub><sup>2-</sup> and NO<sub>3</sub><sup>-</sup> had little effect on the photocatalytic degradation efficiency of TiO<sub>2</sub>. The results indicated that the effects of the inorganic anions on the photocatalytic degradation of phenol depended strongly on the pH, which was related with the adsorption of phenol on the surface of TiO<sub>2</sub>. No significant relationship between the initial pH and the photocatalytic degradation efficiency of TiO<sub>2</sub> was observed in the experiment with the addition of Cl<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup>, indicating that inorganic anions inhibited the photocatalytic degradation efficiency of TiO<sub>2</sub> by their trapping hydroxyl radicals (OH·).
environmental science and information application technology | 2010
Fei Tian; Rongshu Zhu; Lingling Zhang; Weiqian Pan; Feng Ouyang; Wenyi Dong
The effects of various inorganic anions (SO<sub>4</sub><sup>2-</sup>, NO<sub>3</sub><sup>-</sup>, H<sub>2</sub>PO<sub>4</sub><sup>-</sup>, HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup>, F<sup>-</sup>, Cl<sup>-</sup>, Br<sup>-</sup> and I<sup>-</sup>) on the photocatalytic degradation of phenol were investigated under UV light irradiation. In present work, low initial pH value in the presence of H<sub>2</sub>PO<sub>4</sub><sup>-</sup> increased the photocatalytic degradation efficiency of TiO<sub>2</sub>, high initial pH value in the presence of HCO<sub>3</sub><sup>-</sup>, CO<sub>3</sub><sup>2-</sup> and F<sup>-</sup> decreased the photocatalytic degradation efficiency of TiO<sub>2</sub>, and no change of initial pH value in the presence of SO<sub>4</sub><sup>2-</sup> and NO<sub>3</sub><sup>-</sup> had little effect on the photocatalytic degradation efficiency of TiO<sub>2</sub>. The results indicated that the effects of the inorganic anions on the photocatalytic degradation of phenol depended strongly on the pH, which was related with the adsorption of phenol on the surface of TiO<sub>2</sub>. No significant relationship between the initial pH and the photocatalytic degradation efficiency of TiO<sub>2</sub> was observed in the experiment with the addition of Cl<sup>-</sup>, Br<sup>-</sup> or I<sup>-</sup>, indicating that inorganic anions inhibited the photocatalytic degradation efficiency of TiO<sub>2</sub> by their trapping hydroxyl radicals (OH·).
international conference on energy and environment technology | 2009
Wenyi Dong; Zijun Dong; Rongshu Zhu; Yang Dong; Feng Ouyang
Batch experiments were conducted to make a comparison in bromate removal between the silver-supported activated carbon (silver-AC) and virgin grander activated carbon(GAC). The probable mechanism of the better behavior of silver-AC was discussed. The effect of initial bromate concentration, pH and co-exist anions were also investigated in the study. Results showed that the removal efficiency of bromate increased about 25% by using silver-AC, a much better removal. Bromate reduction by silver-AC increases as the solution pH decreases. And the bigger the initial concentration was, the larger of BrO3- removal capacity by silver-AC was. Cl-¿F- and Br- had a slight effect on the removal of BrO3- while SO42-¿CO32-¿NO3- and PO43- showed a stronger influence. The affinity of the anions for silver-AC sites decreased in the following order CO32- ≫ PO43-≫ SO42- ≫ NO3- ≫ Br-≫ Cl-≫ F- when the co-exist anion concentration was 10mg/L.
International Journal of Hydrogen Energy | 2016
Fei Tian; Rongshu Zhu; Jian Zhong; Peng Wang; Feng Ouyang; Gang Cao
Reaction Kinetics, Mechanisms and Catalysis | 2012
Zijun Dong; Wenyi Dong; Feiyun Sun; Rongshu Zhu; Feng Ouyang
Archive | 2010
Wenyi Dong; Yang Dong; Zijun Dong; Liu Jun; Xiaona Zhang; Rongshu Zhu
Renewable Energy | 2017
Rongshu Zhu; Fei Tian; Sainan Che; Gang Cao; Feng Ouyang
International Journal of Hydrogen Energy | 2017
Rongshu Zhu; Fei Tian; Gang Cao; Feng Ouyang
International Journal of Hydrogen Energy | 2017
Yong Qiu; Feng Ouyang; Rongshu Zhu