Collaborative Research: Advanced Oxidation Processes for the Control of Iodinated Disinfection Byproducts in Drinking Water

在传统的水处理工艺中，氯等化学氧化剂被广泛用作灭活水传播病原体的消毒剂。然而，氯可以与饮用水源中的各种本底成分（如天然有机物、溴化物和碘化物）发生反应，形成不需要的有毒消毒副产物（DBPs）。目前，美国环保署规定饮用水中11种DBPs的最大污染物水平，包括4种三卤甲烷（THMs）、5种卤乙酸（HAAs）、溴酸盐（BrO-3）和亚氯酸盐（ClO2-）。不受管制的碘化DBPs （I-DBPs）受到越来越多的关注，因为它们的毒性明显高于受管制的DBPs，并且可以损害细胞和DNA。在饮用水水源消毒过程中，氯等化学氧化剂与碘和含碘化合物（如含碘x射线造影剂）发生反应，形成i - dbp。因此，碘和碘化化合物（ic）的氧化和转化为碘酸盐（IO3 -），一种无毒的碘营养微量元素来源，已成为控制和减轻水处理系统中I-DBPs形成的有前途的单元过程。然而，目前的水处理工艺将碘和ic有效转化为碘酸盐的能力受到几个挑战，包括溴化氧化为溴酸盐和有毒的溴化dbp，以及碘/ ic不完全转化为碘酸盐，这也可能导致在最终产品水中形成i - dbp和其他受调节的dbp。该合作项目的目标是探索开发高级氧化工艺（AOPs）和综合处理系统，以有效氧化并将碘和ic转化为碘酸盐，同时最大限度地减少和防止产品饮用水中有毒i - dbp和受调节dbp的形成。该项目的成功完成将通过开发新的基础知识来造福社会，这些知识可以指导设计和部署更有效的水处理工艺和系统，以减轻和消除水消毒过程中i - dbp的形成。通过学生教育和培训，包括指导南达科他州矿业与技术学院的一名研究生和一名本科生以及南达科他州立大学的一名研究生，将为社会带来额外的好处。在饮用水处理中形成的碘化消毒副产物（I-DBPs）在低浓度下具有高毒性，并且已发现具有细胞毒性和基因毒性。碘化物（I -）和碘化x射线造影剂（ICM）是两种最常见的碘源，可在饮用水处理过程中与消毒剂（如氯和氯胺）反应产生I- dbp。碘和碘化化合物（如ICM）氧化和转化为碘酸盐（IO3 -）是一种无毒的碘营养微量元素来源，已成为控制和减轻水处理系统中I-DBPs形成的有前途的单元过程。该项目的总体目标是通过精心选择和优化高级氧化工艺（AOPs）以及将AOPs与传统工艺相结合，推进控制饮用水处理中新兴i - dbp和受调节dbp所需的基础科学和工程知识。该研究的核心指导假设是，成功控制饮用水处理系统中新出现的i -DBP和受调节的DBP需要碘种和碘化化合物的有效氧化和转化为碘酸盐，仔细管理溴化物的形成，以及在消毒前部分（适当）去除DBP前体NOM（天然有机物质）。本研究的具体目标是：1)研究高铁酸盐（Fe[VI]）、臭氧（O3）、紫外光解及O3的紫外光解等AOPs的利用，优化碘和ICM氧化生成碘酸盐；2)研究AOPs与常规工艺（包括氯化和活性炭吸附）的整合，以最大限度地减少I-DBPs和调节DBPs的形成；3)发展碘种类和I-DBPs的测量分析方法，揭示和量化碘和ICM向I-DBPs和总有机碘的转化途径。该项目的成功完成有可能促进对AOPs对无机和有机碘物种/化合物的反应性和转化的基本理解，以指导碘源特异性处理工艺的设计和开发，从而有效减轻水处理系统中i - dbp和受调节dbp的影响。为了实现该项目的教育和培训目标，首席调查员（pi）建议利用南达科他州矿业与技术学院（SDSMT）和南达科他州立大学的现有计划招募和指导女学生参与该项目。此外，pi计划与饮用水处理专业人员进行互动和合作，以应对南达科他州的水质挑战，参与当地社区外展活动，并与SDSMT艾芬豪国际中心合作，吸引和指导来自非洲大陆的国际学生。该奖项反映了美国国家科学基金会的法定使命，并通过使用基金会的知识价值和更广泛的影响审查标准进行评估，被认为值得支持。

Chemical oxidants such as chlorine are widely utilized as disinfectants to inactivate waterborne pathogens in conventional water treatment processes. However, chlorine can react with various background constituents in drinking water sources (e.g., natural organic matter, bromide, and iodide) to form undesirable and toxic disinfection byproducts (DBPs). Currently, the US EPA regulates the maximum contaminant levels (MCLs) of 11 DBPs in drinking water including 4 trihalomethanes (THMs), 5 haloacetic acids (HAAs), bromate (BrO-3), and chlorite (ClO2-). Unregulated iodinated DBPs (I-DBPs) are receiving increased attention as they are significantly more toxic than the regulated DBPs and can damage cells and DNA. I-DBPs are formed when chemical oxidants such as chlorine react with iodine and iodinated compounds (e.g., iodinated X-ray contrast media) during the disinfection of drinking water sources. Thus, the oxidation and conversion of iodine and iodinated compounds (ICs) to iodate (IO3–), a nontoxic source of iodine nutritional trace element, has emerged as a promising unit process to control and mitigate the formation of I-DBPs in water treatment systems. However, the ability of current water treatment processes to efficiently convert iodine and ICs to iodate suffer from several challenges including the concurrent oxidation of bromide to bromate and toxic brominated DBPs, and the incomplete transformation of iodine/ICs to iodate which can also lead to the formation of I-DBPs and other regulated DBPs in the final product water. The goal of this collaborative project is to explore the development of advanced oxidation processes (AOPs) and integrated treatment trains that can efficiently oxidize and convert iodine and ICs to iodate while minimizing and preventing the formation of toxic I-DBPs and regulated DBPs in the product drinking water. The successful completion of this project will benefit society through the development of new fundamental knowledge that could guide the design and deployment of more effective water treatment processes and systems for mitigating and eliminating and the formation of I-DBPs during water disinfection. Additional benefits to society will be achieved through student education and training including the mentoring of one graduate student and one undergraduate at the South Dakota School of Mines and Technology and one graduate student at South Dakota State University. Iodinated disinfection byproducts (I-DBPs) formed in drinking water treatment are highly toxic at low concentrations and have been found to be cytotoxic and genotoxic. Iodide (I–) and iodinated X-ray contrast media (ICM) are the two most common iodine sources that can react with disinfectants (e.g., chlorine and chloramines) to produce I-DBPs during drinking water treatment. The oxidation and conversion of iodine and iodinated compounds such as ICM to iodate (IO3–), a nontoxic source of iodine nutritional trace element, has emerged as promising unit process to control and mitigate the formation of I-DBPs in water treatment systems. The overarching goal of this project is to advance the fundamental science and engineering knowledge required to control emerging I-DBPs and regulated DBPs in drinking water treatment through careful selection and optimization of advanced oxidation processes (AOPs) and integration of the AOPs with conventional processes. The core guiding hypothesis of the proposed research is that the successful control of emerging I-DBPs and regulated DBPs in drinking water treatment systems would require the efficient oxidation and conversion of iodine species and iodinated compounds to iodate, the careful management of bromide formation, and the partial (decent) removal of NOM (Natural Organic Matter), a DBP precursor, prior to disinfection. The specific objectives of the research are to 1) to investigate the utilization of AOPs, including ferrate (Fe[VI]), ozone (O3), UV photolysis, and UV photolysis with O3, to optimize the oxidation of iodine and ICM to iodate; 2) investigate the integration of AOPs with conventional processes, including chlorination, and activated carbon sorption, to minimize the formation of both I-DBPs and regulated DBPs; and 3) develop analytical methods for measurement of iodine species and I-DBPs to unravel and quantify the transformation pathways of iodine and ICM to I-DBPs and total organic iodine. The successful completion of this project has the potential to advance the fundamental understanding of the reactivity and transformations of inorganic and organic iodine species/compounds by AOPs to guide the design and development of iodine source-specific treatment processes for effective mitigation of both I-DBPs and regulated DBPs in water treatment systems. To implement the education and training goals of this project, the Principal Investigators (PIs) propose to leverage existing programs at the South Dakota School of Mines and Technology (SDSMT) and South Dakota State University to recruit and mentor female students to work on the project. In addition, the PIs plan to interact and collaborate with drinking water treatment professionals to address water quality challenges in South Dakota, engage in local community outreach events, and collaborate with the SDSMT Ivanhoe International Center to engage and mentor international students from the African continent.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.