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羟基氧化铁催化臭氧氧化对滤后水卤乙酸生成势的影响
摘要点击 1884  全文点击 1340  投稿时间:2005-07-04  修订日期:2005-09-27
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中文关键词  臭氧  催化臭氧氧化  羟基氧化铁  卤乙酸生成势  溴离子  重碳酸根
英文关键词  ozone  catalytic ozonation  FeOOH  HAA5FP  bromide  bicarbonate
作者单位
张涛 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
鲁金凤 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
马军 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
陈忠林 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
申素芳 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
王群 哈尔滨工业大学市政环境工程学院 哈尔滨150090 
中文摘要
      考察了滤后水经过单独臭氧氧化和羟基氧化铁(FeOOH)催化臭氧氧化后5种卤乙酸生成势(HAA5FP)的生成情况.研究了氧化时间、溴离子浓度、滤后水pH值、碱度和O3投量对2种氧化方式下HAA5FP的影响规律.发现该滤后水氯化后的HAA种类为二氯乙酸(DCAA)、三氯乙酸(TCAA)及溴离子存在时有二溴乙酸(DBAA).无溴离子存在时,催化臭氧氧化在5~20min内使得HAA5FP比臭氧氧化后的降低9.5%~18.3%.溴离子浓度增加使HAA5FP减少,催化臭氧氧化后HAA5FP也比臭氧氧化后低更多.中性pH时,催化臭氧氧化比臭氧氧化有更明显的控制HAA5FP的优势.重碳酸盐碱度升高使HAA5FP降低,且2种氧化后HAA5FP的差别减小.O3/TOC比值为0.45~1.43的臭氧投量范围内,催化臭氧氧化后HAA5FP比臭氧氧化后减少11.2%~28.0%.催化臭氧氧化对滤后水HAA5FP的影响与FeOOH催化臭氧生成羟基自由基的特点密切相关.
英文摘要
      Formation potential of five haloacetic acids(HAA5FP) of a filtered surface water was studied after ozonation alone and catalytic ozonation with a ferric hydroxide(FeOOH).Factors studied were oxidation time,bromide,pH,bicarbonate alkalinity,and ozone dosages.The haloacetic acids detected were dichloroacetic acid(DCAA),trichloroacetic acid(TCAA),and dibromoacetic acid(DBAA) when bromide existed.The catalytic ozonation caused a reduction of HAA5FP of the non-bromide containing water for 9.5%~18.3% compared to that of ozonation in 5~20 minutes.Incremental addition of bromide led to a much lower HAA5FP after catalytic ozonation than that after ozonation.HAA5FP of the water at neutral pH was higher than that at acidic and basic conditions.Catalytic ozonation showed a most advantageous potential in controlling HAA5FP over ozonation at neutral pH.The HAA5FP decreased as bicarbonate concentration increased,and the disparity between ozonation and catalytic ozonation was also reduced.The HAA5FP after catalytic ozonation was 11.2% to 28.0% lower than that after ozonation while the ratio of O3/TOC ranging from 0.45 to 1.43.The effect of catalytic ozonation on HAA5FP of the water is closely related to its enhanced generation of hydroxyl radicals in catalytic process.

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