DocumentCode
527138
Title
Notice of Retraction
Process mechanism of formaldehyde degradation in aqueous solution using the UV-Fenton method
Author
Jiantao Liang ; Xiangxuan Liu ; Yunchao Wang
Author_Institution
No. 503 Fac., Xi´an Res. Inst. of High Technol., Xi´an, China
Volume
3
fYear
2010
fDate
17-18 July 2010
Firstpage
298
Lastpage
301
Abstract
Notice of Retraction
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
This study was performed to further reveal the reaction mechanism and kinetic characters of UV-Fenton process for the degradation of formaldehyde (HCHO) in a batch photochemical reactor. The concentration changes of hydrogen peroxide, ferrous ions, and the intermediate products were analyzed. Through comparing the rate constants (k) of H2O2 consumption and the variation of Fe2+ concentration in the UVH2O2, Fenton and UV-Fenton processes, it indicates that the Fe2+ and the UV light has a synergistic effect for the degradation of HCHO in the UV-Fenton system. The introduction of UV accelerates the reduction of Fe3+, and makes the cycle of iron obtain more paths. The products in the UV-Fenton reaction were analyzed by a gas chromatography-mass spectrometry and a chemical oxygen demand analyzer. Based on the results, the reaction pathways of HCHO degradation in the UV-Fenton system were proposed. The rate constants of the two consecutive first-order reactions in the degradation of HCHO are respectively k1 = 0.543 min-1 and k2 = 0.045 min-1. The mineralizing of formic acid is the rate-controlled step of the reaction.
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
This study was performed to further reveal the reaction mechanism and kinetic characters of UV-Fenton process for the degradation of formaldehyde (HCHO) in a batch photochemical reactor. The concentration changes of hydrogen peroxide, ferrous ions, and the intermediate products were analyzed. Through comparing the rate constants (k) of H2O2 consumption and the variation of Fe2+ concentration in the UVH2O2, Fenton and UV-Fenton processes, it indicates that the Fe2+ and the UV light has a synergistic effect for the degradation of HCHO in the UV-Fenton system. The introduction of UV accelerates the reduction of Fe3+, and makes the cycle of iron obtain more paths. The products in the UV-Fenton reaction were analyzed by a gas chromatography-mass spectrometry and a chemical oxygen demand analyzer. Based on the results, the reaction pathways of HCHO degradation in the UV-Fenton system were proposed. The rate constants of the two consecutive first-order reactions in the degradation of HCHO are respectively k1 = 0.543 min-1 and k2 = 0.045 min-1. The mineralizing of formic acid is the rate-controlled step of the reaction.
Keywords
chemical reactors; chromatography; hydrogen compounds; iron compounds; mass spectroscopy; reaction kinetics; wastewater treatment; HCHO; UV-Fenton method; aqueous solution; batch photochemical reactor; chemical oxygen demand analyzer; ferrous ion; formaldehyde degradation; formic acid; gas chromatography; hydrogen peroxide; iron; kinetic character; mass spectrometry; rate constant; reaction mechanism; Acceleration; Monitoring; UV-Fenton; formaldehyde; process mechanism; rate constants;
fLanguage
English
Publisher
ieee
Conference_Titel
Environmental Science and Information Application Technology (ESIAT), 2010 International Conference on
Conference_Location
Wuhan
Print_ISBN
978-1-4244-7387-8
Type
conf
DOI
10.1109/ESIAT.2010.5568361
Filename
5568361
Link To Document