首页> 外文会议>Water quality technology conference and exposition (2005 WQTC conference proceedings) >Concentration and inactivation of bacteria, spores, viruses, andprotozoa from large volumes of drinking water
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Concentration and inactivation of bacteria, spores, viruses, andprotozoa from large volumes of drinking water

机译:大量饮用水中细菌,孢子​​,病毒和原生动物的浓缩和灭活

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A single sample concentration and recovery procedure that can be used for bacteria, protozoa,rnand viruses will greatly improve the ability of water utilities and other agencies to respond torncontamination events. However, it is critical to minimize exposure of sample collectors tornpotential biological and chemical hazards in contaminated water. Therefore, the objective of thisrnstudy was to develop a pathogen detection approach comprising inactivation of microorganismsrnby ultraviolet (UV) light irradiation in a flow through device followed by ultrafiltration (UF) tornconcentrate the sample. Small-scale, low-pressure, flow-through UV lamps achieved inactivationrnlevels of 3-log10 with a UV dose of 35 mJ/cm2 for MS-2 compared to 4-log10 at 140 mJ/cm2 forrnB. subtilis spores. Consequently, a dose of 200 mJ/cm2 was selected as a target that shouldrnprovide an acceptable level of operator safety in the event of contaminated samples beingrncollected. UF involved recirculation of 100 L spiked drinking water samples through 65Krnhollow-fiber capsules, providing a concentration factor of 133 – 1,000 . Average recoveryrnefficiencies were 68% for MS-2, 76% for echovirus 1, 60% for B. subtilis spores, 57% forrnSalmonella typhimurium, 86% for Cryptosporidium parvum, and 56% for Encephalitozoonrnintestinalis. Non-UV irradiated concentrates were compatible with all conventional culturingrnmethods, infectivity assays, and microscopic detection methods. This work demonstrated thernfeasibility of inactivating pathogens using a small-scale UV device and simultaneous recovery ofrnviruses, protozoa, bacteria, and spores from large volumes of drinking water by UF. Currentrnwork involves integrating the UV and UF units into a single system, assessing the impact of UVrnirradiation on the ability to detect target pathogens by culture-independent molecular methods,rnand evaluating whether doses that are high enough to destroy chemical contaminants willrninterfere with molecular detection of pathogens.
机译:可用于细菌,原生动物,蠕虫和病毒的单一样品浓缩和回收程序将大大提高自来水公司和其他机构对污染事件的响应能力。但是,至关重要的是最大程度地减少样品收集器在污水中对潜在的生物和化学危害的暴露。因此,本研究的目的是开发一种病原体检测方法,包括通过流通设备中的紫外线(UV)照射灭活微生物,然后超滤(UF)浓缩样品。与140 mJ / cm2 forrnB的4-log10相比,小尺寸,低压,流通式UV灯对MS-2的灭活水平达到3-log10,UV剂量为35 mJ / cm2。枯草芽孢。因此,选择200 mJ / cm2的剂量作为目标,如果收集了受污染的样品,则应提供可接受的操作员安全水平。超滤涉及通过65克空心纤维胶囊对100升加标饮用水样品进行再循环,其浓缩系数为133 – 1,000。 MS-2的平均恢复效率为68%,回声病毒1为76%,枯草芽孢杆菌孢子为60%,鼠伤寒沙门氏菌为57%,小隐孢子虫为86%,脑肠炎为56%。非紫外线辐照浓缩物与所有常规培养方法,感染性测定法和显微检测方法兼容。这项工作证明了使用小型紫外线设备灭活病原体的可行性,并通过超滤同时从大量饮用水中回收了病毒,原生动物,细菌和孢子。当前的工作涉及将UV和UF单元集成到一个系统中,通过与培养无关的分子方法评估UV辐射对检测目标病原体能力的影响,并评估是否足以破坏化学污染物的剂量会干扰病原体的分子检测。

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