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Efficacy of ultraviolet germicidal irradiation of upper-room air in inactivating airborne bacterial spores and mycobacteria in full-scale studies

机译:大规模研究中紫外线对室内空气的杀菌作用灭活了空气中的细菌孢子和分枝杆菌

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The efficacy of ultraviolet germicidal irradiation (UVGI) for inactivating airborne bacterial spores and vegetative mycobacteria cells was evaluated under full-scale conditions. Airborne bacteria inactivation experiments were conducted in a test room (87 m(3)), fitted with a modern UVGI system (216W all lamps operating, average upper zone UV irradiance 42 +/- 19 muW cm(-2)) and maintained at 25degreesC and 50% relative humidity, at two ventilation rates (0 and 6 air changes per hour). Bacillus subtilis (spores), Mycobacterium parafortuitum, and Mycobacterium bovis BCG cells were aerosolized continuously into the room such that their numbers and physiologic state were comparable both with and without the UVGI and ventilation system operating. Air samples were collected using glass impingers (9 breathing-zone locations) and multi-stage impactors, and collected bacteria were quantified using direct microscopy and standard culturing assays. UVGI reduced the room-average concentration of culturable airborne bacteria between 46% and 80% for B. subtilis spores, between 83% and 98% for M. parafortuitum, and 96-97% for M. bovis BCG cells, depending on the ventilation rate. An additional set of experiments, in which M. parafortuitum was aerosolized into the test room and then allowed to decay under varying UVGI and ventilation rates, yielded an inactivation rate of 16+/-1.2 h(-1) for the UVGI system, all lamps operating. The Z value (inactivation rate normalized to UVGI irradiance) was estimated to be 1.2+/-0.15 x 10(-3) cm(2) muW(-1) s(-1) for aerosolized M. parafortuitum at 50% relative humidity. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 37]
机译:在全面条件下评估了紫外线杀菌辐射(UVGI)灭活空气中细菌孢子和无性分枝杆菌细胞的功效。空气传播的细菌灭活实验在装有现代UVGI系统的试验室(87 m(3))中进行(所有灯工作216W,上部区域的平均紫外线辐照度为42 +/- 19 muW cm(-2)),并保持在25摄氏度和50%相对湿度,两个通风速率(每小时换气0和6)。将枯草芽孢杆菌(孢子),副猪分枝杆菌和牛分枝杆菌BCG细胞连续雾化到房间中,这样,无论是否使用UVGI和通风系统,它们的数量和生理状态都是可比的。使用玻璃撞击器(9个呼吸区域位置)和多级撞击器收集空气样本,并使用直接显微镜和标准培养测定法对收集的细菌进行定量。 UVGI将枯草芽孢杆菌孢子的可培养空气传播细菌的室内平均浓度降低了46%至80%,副手念珠菌降低了83%至98%,牛分枝杆菌BCG细胞降低了96-97%,这取决于通风情况率。另一组实验是将副伤寒沙门氏菌雾化到测试室中,然后在变化的UVGI和通风速率下衰减,对于UVGI系统,灭活速率为16 +/- 1.2 h(-1),所有灯工作。在50%的相对湿度下,雾化的副气单胞菌的Z值(相对于UVGI辐照度的失活率标准化)估计为1.2 +/- 0.15 x 10(-3)cm(2)muW(-1)s(-1) 。 (C)2002 Elsevier Science Ltd.保留所有权利。 [参考:37]

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