Department of Chemical Engineering, University of Saskatchewan, 57 Campus Drive, Saskatoon, SK S7N 5A9, Canada.
Environ Technol. 2010 Jan;31(1):47-52. doi: 10.1080/09593330903338403.
The oxidation of phenol by Fenton's reagent was investigated in a medium suitable for bioremediation. An experimental design approach, based on a central composite rotatable design, was used to quantify the effects of H2O2 concentration (2000 to 5000 mg 1(-1)) and FeSO4.7H2O concentration (500 to 2000 mg 1(-1)). Performance of the chemical oxidation by Fenton's reagent was evaluated by determining the percentage of phenol oxidized at equilibrium. The analysis of variance test indicated that both H2O2 and FeSO4.7H2O concentrations had a positive effect on phenol oxidation. Hydrogen peroxide concentration was the dominating parameter for the removal of phenol by Fenton's reagent. The optimal concentrations of H2O2 and FeSO4.7H2O for complete oxidation of 2000 mg 1(-1) phenol in the medium were found to be 4340 mg 1(-1) and 1616 mg 1(-1), respectively, at 25 degrees C and pH 3. Oxidation of phenol in the culture medium was found to be significantly different than in pure water.
芬顿试剂氧化苯酚的研究在适合生物修复的介质中进行。基于中心复合旋转设计的实验设计方法用于量化 H2O2 浓度(2000 至 5000mg/L)和 FeSO4.7H2O 浓度(500 至 2000mg/L)的影响。通过测定平衡时苯酚氧化的百分比来评估芬顿试剂的化学氧化性能。方差分析测试表明,H2O2 和 FeSO4.7H2O 浓度均对苯酚氧化有积极影响。过氧化氢浓度是芬顿试剂去除苯酚的主要参数。在 25°C 和 pH3 下,完全氧化介质中 2000mg/L 苯酚所需的 H2O2 和 FeSO4.7H2O 的最佳浓度分别为 4340mg/L 和 1616mg/L。在培养基中苯酚的氧化明显不同于在纯水中。