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An assessment of the checkpoint bioassay concept for full scale wastewater UV reactor validation

机译:全面废水UV反应器验证的检查点生物测定概念评估

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摘要

In an effort to help policy makers and manufacturers understand the impact of parameternuncertainties on UV reactor performance, a numerical bioassay model was developed by integratingna UV reactor model based on computational fluid dynamics with a Monte Carlo model developed tonaccount for parameter uncertainty. For the model implemented, it was determined that reactornperformance uncertainty was less than 6%. The integrated model was used to evaluate severalncheckpoint bioassay criteria including one currently used by the California Department of PublicnHealth. The model showed that these criteria failed to take into account the fact that in an ideal case,na full scale reactor will pass a single checkpoint test 50% of the time. In reality, differences innequipment measurement errors between the system validation and checkpoint bioassay, andnlimitations of the power law form of the dose monitoring equation in accurately representing systemnvalidation data will result in poorer than expected performance. It was suggested that suchncheckpoint criteria be modified by crediting the inherent over-sizing of full scale reactors.
机译:为了帮助决策者和制造商了解参数不确定性对紫外线反应器性能的影响,通过将基于计算流体动力学的紫外线反应器模型与为参数不确定性开发的蒙特卡洛模型相集成的紫外线反应器模型,开发了数值生物测定模型。对于实施的模型,已确定反应堆性能不确定性小于6%。集成模型用于评估多个ncheckpoint生物测定标准,包括加利福尼亚公共卫生部门当前使用的标准。该模型表明,这些标准没有考虑到在理想情况下,全规模反应堆将在50%的时间内通过单个检查点测试这一事实。实际上,系统验证和检查点生物测定之间的设备测量误差的差异,以及在准确表示系统验证数据时剂量监测方程的幂律形式的局限性,将导致性能不及预期。建议通过考虑固有规模的全尺寸反应堆来修改这种检查点标准。

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