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Effect of nitrification on lead corrosion in chloraminated distribution systems.

机译:硝化作用对氯化分配系统中铅腐蚀的影响。

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摘要

Water treatment facilities have been shifting from using chlorination to chloramination as a primary disinfectant since 2004, when the EPA enacted the Disinfectants/Disinfection By-Products (D/DBP) Rule mandating the decrease of DBPs. After the switch to chloramination, an unexpected lead concentration increase was detected in the Washington, D. C., and Greenville, NC water systems. These increases may be associated with the switch from chlorination to chloramination. Decomposition of chloramines results in higher ammonia loading to drinking water distribution systems, which may increase nitrification. Nitrifying bacteria may facilitate lead corrosion via two mechanisms: use of nitrite or nitrate as an alternative electron acceptor and destruction of alkalinity leading to a reduction of pH.;This project explored the roles that nitrifying bacteria play in lead corrosion in drinking water distribution systems. Hypothesized lead corrosion factors provided by nitrification (the presence of nitrate, nitrite, and an acidic environment) were imposed under abiotic conditions. The effect of nitrifying bacteria on lead corrosion was also examined. The effectiveness of several lead corrosion inhibitors (orthophosphate, zinc orthophosphate, alkalinity dosing, and pH control) was examined in the presence of nitrifying bacteria and under abiotic conditions. Nitrifying bacteria were also tested for tolerance to different concentrations of chloramines.;The presence of 2 mM nitrate or nitrite significantly increased lead corrosion. Nitrate served as an electron acceptor in the corrosion process. Lead corrosion occurred concurrently with the disappearance of nitrate and formation of nitrite. Reduction of nitrite was not quantified despite increased lead corrosion. Lead corrosion, arising from abiotic denitrification, was greater for aged coupons than for freshly cleaned coupons in the presence of nitrate. The presence of an acidic environment also significantly increased lead corrosion. When nitrifying bacteria were allowed to grow, lead corrosion factors (the presence of nitrite and an acidic environment) developed. Increased lead corrosion occurred in the presence of ammonia bio-oxidation to nitrite. Lead corrosion was higher for aged coupons than freshly cleaned coupons in biotic treatments. This suggested that the primary cause of lead corrosion for biotic treatments with a freshly cleaned coupon was the development of an acidic environment while biotic treatments with an aged coupon were susceptible to development of an acidic environment and abiotic denitrification of nitrite.;Under biotic conditions, total lead concentrations were significantly reduced for orthophosphate, pH control, and zinc orthophosphate treatments. pH control showed the greatest reduction in lead corrosion (86.9%). Zinc orthophosphate inhibited the growth of nitrifying bacteria and reduced total lead concentrations by 56.2%. Orthophosphate reduced total lead concentrations by 30.1%. Orthophosphate and alkalinity treatments also reduced total lead concentrations under abiotic conditions.;Chloramine doses as low as 0.10 mg/L Cl2 effectively inhibited ammonia bio-oxidation to nitrite when added to an AOB culture growing in a defined medium. Chloramine doses of 0.10 or 0.25 mg/L Cl2 were not inhibitory when added to an AOB culture following four days of growth in a defined mineral medium, in the absence of chloramine. Chloramine doses as low as 0.10 mg/L Cl2 effectively inhibited ammonia bio-oxidation to nitrite when added to an AOB culture growing in tap water, when the chloramine was added immediately or following eight days of growth in tap water in the absence of chloramine.
机译:自2004年EPA颁布强制要求减少DBP的《消毒剂/消毒副产物(D / DBP)规则》以来,水处理设施已从使用氯化法转变为使用氯化法作为主要消毒剂。转换为氯化胺后,在华盛顿特区和北卡罗来纳州格林维尔的水系统中发现了意外的铅浓度增加。这些增加可能与从氯化反应转向氯化反应有关。氯胺的分解会导致饮用水分配系统中氨含量的增加,从而增加硝化作用。硝化细菌可能通过两种机制促进铅腐蚀:使用亚硝酸盐或硝酸盐作为替代电子受体和破坏碱度导致pH降低。该项目探讨了硝化细菌在饮用水分配系统中铅腐蚀中的作用。在非生物条件下施加了由硝化作用(假设存在硝酸盐,亚硝酸盐和酸性环境)提供的假定的铅腐蚀因子。还检查了硝化细菌对铅腐蚀的影响。在存在硝化细菌的情况下以及在非生物条件下,检查了几种铅腐蚀抑制剂(正磷酸盐,正磷酸盐锌,碱度和pH值控制)的有效性。还测试了硝化细菌对不同浓度的氯胺的耐受性。2 mM硝酸盐或亚硝酸盐的存在显着增加了铅腐蚀。硝酸盐在腐蚀过程中用作电子受体。铅腐蚀与硝酸盐消失和亚硝酸盐形成同时发生。尽管铅腐蚀增加,但亚硝酸盐的还原没有量化。非生物性反硝化引起的铅腐蚀,在硝酸盐存在下,老化的试样比刚清洗过的试样要大。酸性环境的存在也显着增加了铅腐蚀。当硝化细菌生长时,会产生铅腐蚀因子(存在亚硝酸盐和酸性环境)。在氨生物氧化为亚硝酸盐的情况下,铅腐蚀增加。在生物处理中,老化试样的铅腐蚀高于新鲜清洗的试样。这表明使用新鲜清洁的试样进行生物处理的铅腐蚀的主要原因是酸性环境的发展,而使用老化的试样进行的生物处理易受酸性环境的影响和亚硝酸盐的非生物反硝化作用;在生物条件下,对于正磷酸盐,pH控制和正磷酸盐锌处理,总铅浓度显着降低。 pH控制显示最大程度的铅腐蚀降低(86.9%)。正磷酸锌抑制硝化细菌的生长,并使总铅浓度降低56.2%。正磷酸盐使总铅浓度降低了30.1%。在非生物条件下,正磷酸盐和碱度处理还降低了总铅浓度。当添加到在确定的培养基中生长的AOB培养物中时,低至0.10 mg / L Cl2的氯胺剂量可有效抑制氨生物氧化成亚硝酸盐。在不存在氯胺的情况下,在限定的矿物培养基中生长四天后,将0.10或0.25 mg / L Cl2的氯胺剂量添加到AOB培养物中时没有抑制作用。当将氯胺立即添加到自来水中生长的AOB培养物中或在无氯胺的情况下在自来水中生长八天后,低至0.10 mg / L Cl2的氯胺剂量可有效抑制氨生物氧化成亚硝酸盐。

著录项

  • 作者

    Shade, Michael Edward.;

  • 作者单位

    Clemson University.;

  • 授予单位 Clemson University.;
  • 学科 Engineering Environmental.
  • 学位 M.S.
  • 年度 2008
  • 页码 145 p.
  • 总页数 145
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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