Heterogeneous catalytic oxidation of hypophosphite by H2O2: pH effect

2007 ◽  
Vol 55 (12) ◽  
pp. 89-93 ◽  
Author(s):  
C.-C. Hung ◽  
Y.-H. Huang ◽  
C.-Y. Chen

Phosphorus chemicals control key aspects of eutrophication and other environmental process. Hypophosphite (HP) originating from manmade and natural sources was evidenced as present in the environment and was investigated rarely. Recently, iron oxide has been used as a catalyst for oxidising organic contaminants with hydrogen peroxide (i.e. heterogeneous Fenton-like reaction). This study focused mainly on the oxidation of 1.0 mM HP by hydrogen peroxide in the presence of a novel iron oxide catalyst (B1 catalyst) which was prepared through a fluidised-bed Fenton reactor (FBR-Fenton). The background experiments including the oxidation experiment of HP by air only, by H2O2 only and adsorption of HP by B1 catalyst were first elucidated. It was found that HP could not be oxidised at all by air and H2O2 at pH 2.5–12 in 24 hours. On the other hand, it could be adsorbed by B1 catalyst with 89.8% removal at pH 2.5 in 5 hours and complete desorption at pH 11.0. Then, we investigated the effects of pH and Fe leaching from the catalyst on the oxidative efficiency of HP. We found that although the removal rate of HP at pH 2.5 is faster than that at pH 4.0, B1 catalyst has a higher HP oxidation efficiency at pH 4.0 than that at pH 2.5. We conclude that it is a major heterogeneous catalytic oxidation by our novel iron oxide catalyst to oxidise HP at pH 4.0. Also, B1 could be a useful and potential catalyst for the treatment of HP wastewater.

2009 ◽  
Vol 43 (23) ◽  
pp. 8930-8935 ◽  
Author(s):  
Anh Le-Tuan Pham ◽  
Changha Lee ◽  
Fiona M. Doyle ◽  
David L. Sedlak

2001 ◽  
Vol 1 (4) ◽  
pp. 131-138
Author(s):  
M.D. Gurol ◽  
S-S. Lin

This paper describes a novel heterogeneous catalytic oxidation process involving the use of hydrogen peroxide ( H2O2) with granular size iron oxide particles (FeOOH) in aqueous phase. The generation of hydroxyl radical (OH•) in the process is demonstrated through the use of a probe chemical, n-chlorobutane (BuCl). Based on the experimental evidence, it is concluded that the OH•, which is produced through the interaction of H2O2 with the surface sites, reacts with solutes adsorbed on the iron oxide surface, causing oxidation of the organic compounds. The generation rate of OH• increases slightly with increasing pH in the range of 5-9. The oxidation rate of BuCl by OH• is relatively insensitive to the pH and the level of bicarbonate ion in subject water due to low affinity of bicarbonate for the surface. Phosphate, on the other hand, inhibits the oxidation rate by preferential adsorption on the surface. This new process provides a viable alternative to the existing oxidation technologies, especially when water has high alkalinity and/or it is desired to oxidize target compounds that have high affinity for the surface selectively.


Author(s):  
Mirat D. Gurol ◽  
Shu-Sung Lin

AbstractThis paper describes a novel heterogeneous catalytic oxidation process involving the use of hydrogen peroxide (H


1995 ◽  
Vol 31 (6) ◽  
pp. 288-292 ◽  
Author(s):  
�. G. Telyashev ◽  
R. R. Vezirov ◽  
I. R. Yavgil'din ◽  
I. O. Tuktarova ◽  
G. G. Telyashev ◽  
...  

1995 ◽  
Vol 2 (1-4) ◽  
pp. 1-15 ◽  
Author(s):  
Robert J. O'Brien ◽  
Liguang Xu ◽  
Diane R. Milburn ◽  
Yong-Xi Li ◽  
Kenneth J. Klabunde ◽  
...  

Fuel ◽  
1989 ◽  
Vol 68 (5) ◽  
pp. 618-621 ◽  
Author(s):  
T KOTANIGAWA ◽  
S YOKOYAMA ◽  
M YAMAMOTO ◽  
Y MAEKAWA

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