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匈牙利帕克斯核电站周边大气碳监测进展

Advanced atmospheric C monitoring around the Paks Nuclear Power Plant, Hungary.

作者信息

Varga Tamás, Orsovszki Gergely, Major István, Veres Mihály, Bujtás Tibor, Végh Gábor, Manga László, Jull A J Timothy, Palcsu László, Molnár Mihály

机构信息

Isotope Climatology and Environmental Research Centre, Institute for Nuclear Research, Hungarian Academy of Sciences (Atomki), Debrecen, H-4001, P.O Box 51, Hungary; University of Debrecen, Doctoral School of Physics, Debrecen, Hungary.

Isotoptech Ltd, Debrecen, Hungary.

出版信息

J Environ Radioact. 2020 Mar;213:106138. doi: 10.1016/j.jenvrad.2019.106138. Epub 2019 Dec 17.

Abstract

Atmospheric air samples were collected at 9 monitoring stations (A1 to A9) less than 2 km from the Paks Nuclear Power Plant (Paks NPP) and a background station (B24). The monthly integrated CO and total carbon (CO+hydrocarbons (CH)) samples were collected to determine the excess C activity at the vicinity of the NPP. The measurements providing the C/C ratio of the monthly integrated samples were carried out on a MICADAS type AMS at HEKAL. Due to the relatively low CO emission of PWR type Paks reactors and the local Suess effect, there was negligible excess C activity at the investigated stations in the pure CO fraction during the investigated 2 years period (2015-2016). On the contrary, there was a detectable (although minor) excess at every station in the CH fraction. In case of CO, the average ΔC excess was 3.8‰ and the highest measured value was 91.2‰ at the A3 station in February 2015. In case of CH, the average excess was 31.1‰ and the highest measured value was 319.1‰ at the A4 station in February 2016. We applied PC-CREAM 08 modelling to investigate the observed excess C activity at the environmental sampling stations, which depends on the distance from the NPP and the meteorological conditions, such as wind direction and wind speed. Meteorology data was collected at the operating area of the Paks NPP in a meteorology tower. The direct C-14 emission through the 120 m high stacks was measured in the NPP by liquid scintillation counting. These emission data and our model calculations explain the excess activity in the CH fraction at the A4 station, which is located only 915 m far from the NPP's stacks in the prevailing wind direction. The excess activity at A3 station (the farthest unit) probably came from the nearby NPP wastewater discharge point. The recently observed average excess and highest excess data is similar to the published data in former studies (Molnár et al., 2007; Veres et al., 1995) on Paks NPP, the highest CO and CH excess are just a little higher than it was in the earlier studies, but in these former studies, the A3 station was not equipped with a radiocarbon monitoring unit and the level of radiocarbon emission was almost invisible from the wastewater discharge point.

摘要

在距离帕克斯核电站(Paks NPP)不到2公里的9个监测站(A1至A9)以及一个背景站(B24)采集了大气空气样本。采集每月综合一氧化碳(CO)和总碳(CO + 碳氢化合物(CH))样本,以确定核电站附近的过剩碳活性。在HEKAL的一台MICADAS A型加速器质谱仪上对提供每月综合样本的碳 - 碳(C/C)比值的测量进行了分析。由于帕克斯压水堆型反应堆的一氧化碳排放量相对较低以及当地的苏士效应,在2015 - 2016年的调查期间,在所调查的监测站的纯一氧化碳部分中,过剩碳活性可忽略不计。相反,在碳氢化合物部分的每个监测站都有可检测到的(尽管较小)过剩。对于一氧化碳,平均过剩ΔC为3.8‰,2015年2月在A3站测得的最高值为91.2‰。对于碳氢化合物,平均过剩为31.1‰,2016年2月在A4站测得的最高值为319.1‰。我们应用PC - CREAM 08模型来研究环境采样站观测到的过剩碳活性,其取决于离核电站的距离以及气象条件,如风向和风速。气象数据在帕克斯核电站作业区的一座气象塔上收集。通过液体闪烁计数在核电站测量了通过120米高烟囱的直接碳 - 14排放。这些排放数据和我们的模型计算解释了位于盛行风向且距离核电站烟囱仅915米的A4站碳氢化合物部分的过剩活性。A3站(最远的站点)的过剩活性可能来自附近的核电站废水排放点。最近观测到的平均过剩和最高过剩数据与之前关于帕克斯核电站的研究(Molnár等人,2007年;Veres等人,1995年)中公布的数据相似,一氧化碳和碳氢化合物的最高过剩仅比早期研究略高,但在这些早期研究中,A3站没有配备放射性碳监测装置,且从废水排放点几乎看不到放射性碳的排放水平。

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