A. H. Knol, K. Lekkerkerker-Teunissen, C. Houtman, J. Scheideler, A. Ried, J. V. Dijk
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引用次数: 10
摘要
在中试规模上,采用O3 / H2O2(过氧酮)对预处理后的默兹河水体进行深度氧化,研究有机微污染物(OMPs)的转化和溴酸盐的形成。将14种选定的模型化合物定期投加到预处理的河水中,以评估过氧化物酮工艺的效率,并确定水基质的影响。臭氧剂量是模式化合物转化的主要因素,但由于溴酸盐的形成,臭氧剂量受到限制。双氧水的添加量对溴酸盐的转化影响较小,但对溴酸盐的生成有较好的抑制作用。在有限的化学品消耗方面,最大的转化,并符合严格的荷兰饮用水法案,溴酸盐为1g L?1、peroxone的实际设置是6mg L?1双氧水和1.5 mg L?1臭氧。在调查期间,模型化合物的平均转化率为78.9%。水温越高、DOC和碳酸氢盐浓度越低,OMPs的转化率越高。在较高的水温和较低的碳酸氢盐浓度下,溴酸盐的生成量也较高,且与溴化物浓度成正比,高于约32 μ g L。1溴化。可根据(导出的)参数(水温、碳酸氢盐和DOC)对过氧化氢过程进行控制。
Conversion of organic micropollutants with limited bromate formation during the Peroxone process in drinking water treatment
Advanced oxidation with O3 / H2O2 (peroxone) was conducted on pilot plant scale on pre-treated Meuse river water to investigate the conversion of organic micropollutants (OMPs) and the formation of bromate. Fourteen selected model compounds were dosed to the pre-treated river water on a regular basis to assess the efficiency of the peroxone process and to establish the influence of the water matrix. The ozone dose was the main factor in the conversion of the model compounds, however, the ozone dose was limited because of bromate formation. The hydrogen peroxide dosage had only a minor effect on the conversion, but it limited the bromate formation effectively. In terms of limited chemical consumption, maximal conversion and to comply the strict Dutch drinking water act for bromate of 1 ?g L?1, a practical peroxone setting was 6 mg L?1 hydrogen peroxide and 1.5 mg L?1 ozone. During the investigation period, the average conversion of the model compounds was 78.9 %. The conversion of OMPs was higher at higher water temperatures and lower concentrations of DOC and bicarbonate. The bromate formation also was higher at higher water temperature and lower bicarbonate concentration and proportional with the bromide concentration, above a threshold of about 32 ?g L?1 bromide. The peroxone process can be controlled on basis of the (derived) parameters water temperature, bicarbonate and DOC.