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COLLABORATIVE RESEARCH: Virus removal in membrane bioreactors: Role of virus aggregation and adhesion

COLLABORATIVE RESEARCH: Virus removal in membrane bioreactors: Role of virus aggregation and adhesion
合作研究:膜生物反应器中的病毒去除:病毒聚集和粘附的作用
批准号:
1236672
负责人:
Thanh Nguyen
金额:
$19.06万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2016-12-31

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中文摘要
翻译
1236672/1236393 Nguyen/Tarabara好氧膜生物反应器(MBR)已成为市政和工业废水处理的最先进技术。与传统的活性污泥反应器相比,MBR的优点包括占地面积小,出水水质更好。MBR已成为水回用的一种特别有吸引力的处理选择。在再利用应用中或当废水被释放到敏感水体(如娱乐用水)时,去除病毒病原体以使公共健康不受威胁尤为重要。目前缺乏对MBR中病毒命运的全面研究,但需要更广泛地应用MBR技术,包括分散的进水水质变化的水再利用。 PI将系统地研究病毒粘附和聚集对MBR中病毒清除的作用。核心假设是,病毒粘附到胞外聚合物(EPS)和可溶性微生物产物(SMP)的程度与病毒通过膜相反。实验计划包括以下工作:(1)进行实验室规模的好氧膜生物反应器的研究与平板和中空纤维膜的不同孔径;在试验的子集中,操作条件将模拟在密歇根州特拉弗斯城的CH 2 MHill全规模MBR设备中使用的那些,(2)表征从实验室规模MBR系统和全规模MBR装置收获的SMP、EPS和膜生物膜,(3)使用任务2中表征的SMP和EPS定量病毒聚集和粘附到污染膜上,(4)将粘附和聚集与在生物膜发展的不同阶段通过污染膜去除病毒相关联,以及(5)使用细胞培养依赖性方法和定量PCR评估MBR中的病毒去除。 选择腺病毒作为本研究的靶病毒。这些发现将有可能改变MBR的设计标准,特别是因为它们涉及膜的选择。虽然基于MBR的处理依赖于膜以确保适当的分离屏障,但病毒去除并不是设计MBR的标准。随着我们对水的技术,经济和社会态度和方法从单向的资源到废物的方法转向可持续再利用的概念,对处理过的废水的微生物质量进行更严格的控制成为一个何时而不是是否的问题。考虑到这一点,我们看到了我们提出的研究的实际目的,即为不久的将来制定水再利用政策和法规所需的决策过程提供信息。 该项目的成功完成将为重新构思MBR设计和运行提供科学依据,以适应病毒去除作为设计标准和处理目标之一。该项目汇集了一个多元化的PI团队,他们拥有一套免费的技能,包括界面科学,膜工艺和环境微生物学,以及代表全规模MBR设施的工业合作伙伴。由所有PI共同指导的一组研究生和本科生将在结合学术研究,与工业部门合作的实验室研究和国际工作的环境中提供一系列学习机会。我们将组织年度小型研讨会-在UIUC(第1年),MSU(第2年)和特拉弗斯城MBR设施(第3年),项目参与者将展示他们的研究结果,讨论未来的研究并从工业合作伙伴那里获得反馈。
英文摘要
1236672/1236393Nguyen/Tarabara Aerobic membrane bioreactors (MBRs) have become a state-of-the-art technology for municipal and industrial wastewater treatment. Compared to traditional activated sludge reactors, advantages of MBR include smaller footprint and better effluent quality. MBRs have become a particularly attractive treatment choice for water reuse. In reuse applications or when the effluent is released to sensitive water bodies such as recreational water, it is especially important that viral pathogens are removed so that public health is not threatened. Comprehensive studies of virus fate in MBRs are currently lacking yet required for wider application of MBR technology, including decentralized water reuse with variable influent quality. The PIs will systematically investigate the role of virus adhesion and aggregation on virus removal in MBRs. The central hypothesis is that the extent of virus adhesion to extracellular polymeric substances (EPS) and soluble microbial products (SMP) counter-correlates with virus passage through the membrane. The experimental plan consists of the following tasks: (1) conduct bench-scale aerobic MBR studies with flat sheet and hollow fiber membranes of varied pore size; in a subset of tests operating conditions will mimic those used in the CH2M Hill full-scale MBR facility in Traverse City, MI, (2) characterize SMP, EPS, and membrane biofilm harvested from the bench-scale MBR system and the full-scale MBR plant, (3) quantify virus aggregation and adhesion to fouled membranes using SMP and EPS characterized in Task 2, (4) correlate adhesion and aggregation with the removal of virus by fouled membranes at different stages of biofilm development, and (5) evaluate virus removal in MBRs using cell culture-dependent methods and quantitative PCR. Adenovirus is selected as target virus for this study. The findings will have the potential for transforming MBR design criteria particularly as they pertain to membrane selection. While MBR-based treatment relies on the membrane to ensure an appropriate separation barrier, virus removal has not been a criterion in designing MBRs. As our technological, economic and social attitudes and approaches toward water shift from the unidirectional resource-to-waste approach toward the concept of sustainable reuse, stricter control over microbiological quality of treated used water becomes a question of when rather than if. With this in mind, we see the practical end of the research we propose in informing the decision-making process reqiered for the development of water reuse policies and regulations of the near future. Successful completion of this project will provide scientific basis for re-conceptualizing MBR design and operation to accommodate virus removal as one of design criteria and treatment goals. The project brings together a diverse team of PIs with a complimentary set of skills including interfacial science, membrane processes, and environmental microbiology and an industrial partner representing a full-scale MBR facility. A group of graduate and undergraduate students co-advised by all PIs will be provided a range of learning opportunities in an environment that combines academic studies, laboratory research in collaboration with the industrial sector, and international work. We will organize annual mini-symposia - at UIUC (year 1), MSU (year 2), and at the Traverse City MBR facility (year 3) where project participants will present their findings, discuss future research and receive feedback from the industrial partner.
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