Characterization of Gamma-Ray Source-Term in the Vicinity of Metlinsky Pond at the Techa River. Radionuclide Composition of the Source

IF 0.9 Q4 CHEMISTRY, INORGANIC & NUCLEAR Radiochemistry Pub Date : 2024-03-12 DOI:10.1134/S1066362223070081
Yu. G. Mokrov
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Abstract

The paper is aimed at reconstruction of a source term for external exposure of population that inhabited the banks of the Techa River from 1949 to 1956. The composition of γ-emitting nuclides contributing to radiation environment of the river banks and floodplain is also studied. The γ-emitting nuclides entered the river system both in solutions and as industrial and natural suspended matter. The paper considers archive data on measured parameters of radiation contamination of the Techa bottom sediments and riverside area. Results of the present-day radiation surveys of the Techa River show that the distribution of the exposure dose rate has a pronounced spotted and non-monotonic character along the entire river stretch and is due to sedimentation of suspended particles contaminated with the γ-emitting nuclides on the soil surface. The activity of γ-emitting nuclides accumulated in the upper reaches of the river due to sorption of water-soluble radionuclides onto bottom sediments and to sedimentation of contaminated suspended matter on the surface of bottom sediments was calculated using a stationary sorption model and a hydrodynamic model of settling ponds. Until July 1951, when the river runoff did not exceed 1 m3/s, practically all industrial and natural suspended particles settled to and accumulated at the bottom of Metlinsky Pond. Only a small portion of clay particles could enter the river below the dam of Metlinsky Pond. 95Zr and 95Nb are of high importance for reconstruction of the radiation environment in the Techa riverside area, because before 1953 the activity of the bottom sediments in all segments of the river was predominantly determined by these γ-emitting nuclides. There is practically no sorption of 95Nb onto bottom sediments and suspended matter, and the river flow carries predominantly soluble 95Nb species. 95Zr, on the contrary, is strongly sorbed onto bottom sediments and can be transferred for long distances only as suspended matter or bed silt. Until October 1951, the radiation environment along the entire river stretch below Metlinsky Pond was contributed predominantly by 95Nb and was characterized by uniform and stable contamination level in all swampy areas of the floodplain. Vast contamination of the bottom sediments and the floodplain along the entire river stretch by other γ-emitting nuclides (95Zr, 137Cs, 141,144Ce, 103,106Ru, etc.) could result only from “washing” of Metlinsky Pond in October 1951, when the flow rate in the upper reaches of the river was up to 30 m3/s. This was accompanied by intensive stirring-up of the bottom sediments and activity transfer out of Metlinsky Pond.

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Techa 河 Metlinsky 池塘附近伽马射线源的特征。源的放射性核素组成
摘要 本文旨在重建1949年至1956年期间居住在泰察河两岸的居民所受外部照射的源项。本文还研究了造成河岸和洪泛区辐射环境的γ发射核素的组成。γ发射核素以溶液以及工业和自然悬浮物的形式进入河流系统。本文考虑了 Techa 河底沉积物和河岸地区辐射污染测量参数的档案数据。目前对特查河的辐射调查结果表明,辐照剂量率的分布在整个河段具有明显的斑点和非单调性,这是由于土壤表面受γ发射核素污染的悬浮颗粒沉积所致。利用静止吸附模型和沉淀池水动力模型,计算了由于水溶性放射性核素在底层沉积物上的吸附作用和污染悬浮物在底层沉积物表面的沉积作用而在河流上游积累的γ发射核素的放射性活度。直到 1951 年 7 月,当河流径流量不超过 1 立方米/秒时,几乎所有的工业和自然悬浮颗粒都沉降并积聚在梅特林斯基池塘的底部。只有一小部分粘土颗粒可以进入梅特林斯基池大坝下的河流。95Zr 和 95Nb 对于重建 Techa 河沿岸地区的辐射环境具有重要意义,因为在 1953 年之前,该河流所有河段底部沉积物的放射性活度主要是由这些γ发射核素决定的。底层沉积物和悬浮物上几乎没有 95Nb 的吸附,河水主要携带可溶的 95Nb 物种。相反,95Zr 在底层沉积物上的吸附力很强,只能以悬浮物或河床淤泥的形式远距离转移。直到 1951 年 10 月,梅特林斯基池塘以下整个河段的辐射环境主要由 95Nb 构成,其特点是洪泛区所有沼泽地的污染水平均匀而稳定。只有在 1951 年 10 月对梅特林斯基池塘进行 "冲刷 "时,整个河段的底层沉积物和冲积平原才会受到其他γ发射核素(95Zr、137Cs、141,144Ce、103,106Ru 等)的严重污染,当时河流上游的流速高达 30 立方米/秒。与此同时,河底沉积物受到强烈搅动,活动转移到梅特林斯基池塘之外。
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来源期刊
Radiochemistry
Radiochemistry CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
1.30
自引率
33.30%
发文量
51
期刊介绍: Radiochemistry  is a journal that covers the theoretical and applied aspects of radiochemistry, including basic nuclear physical properties of radionuclides; chemistry of radioactive elements and their compounds; the occurrence and behavior of natural and artificial radionuclides in the environment; nuclear fuel cycle; radiochemical analysis methods and devices; production and isolation of radionuclides, synthesis of labeled compounds, new applications of radioactive tracers; radiochemical aspects of nuclear medicine; radiation chemistry and after-effects of nuclear transformations.
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