Kinetics and corrosion products of aqueous nitrate reduction by iron powder without reaction conditions control

• Published in: Journal of environmental sciences (China) 2009, Vol.21 (8), p.1028-1035
• Main Authors: FAN, Xiaomeng, GUAN, Xiaohong, MA, Jun, AI, Hengyu
• Format: Article
• Language: English
• Subjects: Coating; Corrosion; Corrosion products; Hydrogen-Ion Concentration; Iron; Iron - chemistry; Kinetics; nitrate reduction; Nitrates; Nitrates - chemistry; Oxidation-Reduction; Reaction kinetics; Reduction; X-rays; X射线光电子能谱; zero-valent iron; 反应pH值; 条件控制; 水动力学; 涂料产品; 硝酸盐浓度; 腐蚀产物; 还原铁粉
• ISSN: 1001-0742; 1878-7320
• DOI: 10.1016/S1001-0742(08)62378-5

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.