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控制河水中过氧化氢降解的因素,以及河床砂的作用。

Factors controlling the degradation of hydrogen peroxide in river water, and the role of riverbed sand.

机构信息

Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima 739-8521, Japan.

Center for Health and Environmental Risk Research, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan.

出版信息

Sci Total Environ. 2020 May 10;716:136971. doi: 10.1016/j.scitotenv.2020.136971. Epub 2020 Jan 28.

DOI:10.1016/j.scitotenv.2020.136971
PMID:32044480
Abstract

Diurnal changes of HO in river water during mid-summer were investigated. HO in river water increased with the increase in intensity of solar radiation in the morning, and reached a maximum at 14:00, although solar radiation reached a maximum around 12:00. In the afternoon, a gradual decrease in HO was observed, and HO reached a minimum just before sunrise. Degradation rate constants determined using unfiltered river water samples were 0.081-0.161 h, corresponding to a half-life of 4.3-8.5 h. We simulated diurnal changes in HO using a simple formation, accumulation, and degradation model for static water using formation and degradation rate constants. The results of the modeling suggested that in situ degradation rate constants in rivers could be faster than those determined for unfiltered river water samples. Experiments using river sand indicated that riverbed sand could play an important role in HO decay in rivers. We discussed the decomposition process of HO in rivers.

摘要

研究了夏半年河水中 HO 的日变化。尽管太阳辐射在 12:00 左右达到最大值,但河水中的 HO 随着清晨太阳辐射强度的增加而增加,并在 14:00 达到最大值。下午,HO 逐渐减少,HO 在日出前达到最小值。使用未经过滤的河水样本确定的降解率常数为 0.081-0.161 h,半衰期为 4.3-8.5 h。我们使用形成和降解速率常数,通过一个简单的形成、积累和静态水降解模型来模拟 HO 的日变化。建模结果表明,河流中的原位降解速率常数可能比未经过滤的河水样本中确定的速率常数更快。使用河砂进行的实验表明,河床砂在河流中 HO 的衰减中可能起重要作用。我们讨论了河水中 HO 的分解过程。

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