Although considerable research has been conducted on nitrate reduction by zero-valent iron powder （Fe^0）, these studies were mostly operated under anaerobic conditions with invariable pH that was unsuitable for prac...Although considerable research has been conducted on nitrate reduction by zero-valent iron powder （Fe^0）, these studies were mostly operated under anaerobic conditions with invariable pH that was unsuitable for practical application. Without reaction conditions （dissolved oxygen or reaction pH） control, this work aimed at subjecting the kinetics of denitrification by microscale Fe^0 （160-200 mesh） to analysis the factors affecting the denitrification of nitrate and the composition of iron reductive products coating upon the iron surface. Results of the kinetics study have indicated that a higher initial concentration of nitrate would yield a greater reaction rate constant. The reduction rate of nitrate increased with increasing Fe^0 dosage. The reaction can be described as a pseudo-first order reaction with respect to nitrate concentration or Fe^0 dosage. Experimental results also suggested that nitrate reduction by microscale Fe^0 without reaction condition control primarily was an acid-driven surface-mediated process, and the reaction order was 0.65 with respect to hydrogen ion concentration. The analyses of X-ray diffractometry and X-ray photoelectron spectroscopy indicated that a black coating, consisted of Fe2O3, Fe3O4 and FeO（OH）, was formed on the surface of iron grains as an iron corrosion product when the system initial pH was lower than 5. The proportion of FeO（OH） increased as reaction time went on, whereas the proportion of Fe3O4 decreased.展开更多
The initial corrosion behavior of pure zinc in a simulated tropical marine atmosphere was investigated using gravimetric method,scanning electron microscope combined with energy dispersive spectroscopy(SEM-EDS),X-ray ...The initial corrosion behavior of pure zinc in a simulated tropical marine atmosphere was investigated using gravimetric method,scanning electron microscope combined with energy dispersive spectroscopy(SEM-EDS),X-ray diffractometry(XRD),Fourier transform infrared spectrometry(FTIR)and electrochemical impedance spectroscopy(EIS).The kinetics of corrosion process is a decelerating process following the empirical equation D=At^n(n<1).The protectiveness of the corrosion product layer could be attributed to the formation of simonkolleite,Zn5(OH)8Cl2·H2O,which could inhibit the rate determining step,namely charge transfer step,of the electrochemical corrosion process.A model of the evolution process of the product layers formed on zinc was proposed.In addition,the regularity of the corrosion rate of zinc as a function of the NaCl deposition rate can be described by a power function.展开更多
基金supported by the Development Program for Outstanding Young Teachers in Harbin Institute of Technology (No. HITQNJS. 2007. 038)
文摘Although considerable research has been conducted on nitrate reduction by zero-valent iron powder （Fe^0）, these studies were mostly operated under anaerobic conditions with invariable pH that was unsuitable for practical application. Without reaction conditions （dissolved oxygen or reaction pH） control, this work aimed at subjecting the kinetics of denitrification by microscale Fe^0 （160-200 mesh） to analysis the factors affecting the denitrification of nitrate and the composition of iron reductive products coating upon the iron surface. Results of the kinetics study have indicated that a higher initial concentration of nitrate would yield a greater reaction rate constant. The reduction rate of nitrate increased with increasing Fe^0 dosage. The reaction can be described as a pseudo-first order reaction with respect to nitrate concentration or Fe^0 dosage. Experimental results also suggested that nitrate reduction by microscale Fe^0 without reaction condition control primarily was an acid-driven surface-mediated process, and the reaction order was 0.65 with respect to hydrogen ion concentration. The analyses of X-ray diffractometry and X-ray photoelectron spectroscopy indicated that a black coating, consisted of Fe2O3, Fe3O4 and FeO（OH）, was formed on the surface of iron grains as an iron corrosion product when the system initial pH was lower than 5. The proportion of FeO（OH） increased as reaction time went on, whereas the proportion of Fe3O4 decreased.
基金Project (201604046014) supported by Guangzhou Industry-University-Research Collaborative Innovation Alliance Special Program,ChinaProjects (51671197,51601199) supported by the National Natural Science Foundation of China
文摘The initial corrosion behavior of pure zinc in a simulated tropical marine atmosphere was investigated using gravimetric method,scanning electron microscope combined with energy dispersive spectroscopy(SEM-EDS),X-ray diffractometry(XRD),Fourier transform infrared spectrometry(FTIR)and electrochemical impedance spectroscopy(EIS).The kinetics of corrosion process is a decelerating process following the empirical equation D=At^n(n<1).The protectiveness of the corrosion product layer could be attributed to the formation of simonkolleite,Zn5(OH)8Cl2·H2O,which could inhibit the rate determining step,namely charge transfer step,of the electrochemical corrosion process.A model of the evolution process of the product layers formed on zinc was proposed.In addition,the regularity of the corrosion rate of zinc as a function of the NaCl deposition rate can be described by a power function.
