Studies on plutonium in terrigenous air-dust
Studies on plutonium in terrigenous air-dust
批准号:
09640581
负责人:
NAKANISHI Takashi
金额:
$2.18万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1999
中文摘要
为了利用环境钚作为示踪剂估计陆源空气粉尘对海洋的通量,对1993 ~ 1998年在日本金泽采集的空气粉尘样品中的Pu-239、240和Fe进行了测定。采用5级(粒径<1.1 μm、1.1 ~ 2.0 μm、2.0 ~ 3.3 μm、3.3 ~ 7.0 μm、7.0 μm<)安徒生式大容量空气采样器采集空气粉尘样品,每月更换捕集板和备用过滤器;每1-8个月收集一次的空气粉尘作为一个批次进行分析。在上述采样年份和粒径范围内,空气粉尘样品中Pu-239、240和Fe - I的浓度分别在0.1 ~ 10 μBq-Pu/mg-dust和2 ~ 30 μg-Fe/mg-dust之间。在较细的空气粉尘中,Pu/Fe浓度比趋于较高,表明Pu被吸附在陆源空气粉尘表面。通过分析po - 210 / pb - 210活性比air-dust样本收集偶尔几天使用Andersen-type少量空气取样器,从9到140天的明显的浮动时间估计air-dust(颗粒大小:O.06 ~ 0.13μm, O.13 ~ 0.22μm, O.22 ~ 0.33μm, 0.33 ~ 0.52μm, 0.52 ~ 0.76μm, 0.76 ~ 1.3μm, 1.3 ~ 2.5μm, 2.5 ~ 3.9μm, 3.9 ~ 5.7μm, 5.7 ~ 8.5μm, 8.5 ~ 12.1μm)。
英文摘要
For a study to estimate terrigenous air-dust fluxes to oceanic region by using environmental plutonium as a tracer, Pu-239, 240 and Fe were determined in air-dust samples collected in Kanazawa, Japan through the years from 1993 to 1998. The air-dust samples were collected using a five-stages (particle size : <1.1 μm, 1.1〜2.0 μm, 2.0〜3.3 μm, 3.3〜7.0 μm, 7.0 μm<) Andersen-type high-volume air sampler, and catcher plates and backup filter were replaced monthly ; air-dust collected every 1-8 months was analyzed as one batch.Throughout the above mentioned sampling years and particle sizes, the concentrations of Pu-239, 240 and Fe I n the air-dust samples were in a range from 0.1 to 10 μBq-Pu/mg-dust and from 2 to 30 μg-Fe/mg-dust. The Pu/Fe concentration ratios tend to be high in finer air-dust, suggesting that Pu is adsorbed on the surface of terrigenous air-dust. Through the analyses of Po-210/Pb-210 activity ratios in air-dust samples collected occasionally for a few days using Andersen-type low-volume air sampler, from 9 to 140 days were estimated as the apparent floating time of air-dust (particle size : O.06〜0.13 μm, O.13〜0.22 μm, O.22〜0.33 μm, 0.33〜0.52 μm, 0.52〜0.76 μm, 0.76〜1.3 μm, 1.3〜2.5 μm, 2.5〜3.9 μm, 3.9〜5.7 μm, 5.7〜8.5 μm, 8.5〜12.1 μm).
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M. A. Haque, T. Nakanishi: "Host phase of ィイD1239,240ィエD1Pu and ィイD1241ィエD1Am in deep-sea sediment"J. Radioanal. Nucl. Chem.. 239(3). 565-569 (1999)
M. A. Haque,T. Nakanishi:“深海沉积物中 D1239、240D1Pu 和 D1241D1Am 的宿主相”J. Radioanal Chem. 239(3) (1999)。
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M.A.Haque,T.Nakanishi: "Chemical dissolution of total content of fallout plutonium in deep-sea sediment"J.Radional.Nucl.Chem.. 241(3). 575-579 (1999)
M.A.Haque,T.Nakanishi:“深海沉积物中沉降钚总含量的化学溶解”J.Radional.Nucl.Chem.. 241(3)。
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Y. Miyamoto: "Interferences in neutron and photon activation analysis"J. Radioanal. Nucl. Chem.. 239(1). 165-175 (1999)
Y. Miyamoto:“中子和光子激活分析中的干扰”J。
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Y.Nozaki,M.Yamada,T.Nakanishi,Y.Nagaya,K.Nakamura,K.Shitashima,H.Tsubota: "The distribution of radionuclides and some trace metals in the water columns of the Japan and Bonin trenches" Occanologica Acta. 印刷中.
Y. Nozaki、M. Yamada、T. Nakanishi、Y. Nagaya、K. Nakamura、K. Shitashima、H. Tsubota:“日本和小笠原海沟水柱中放射性核素和一些痕量金属的分布”《海洋学学报》正在打印。
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Y. Miyamoto, H. Haba, A. Kajikawa, K. Masumoto, T. Nakanishi, K. Sakamoto: "Interferences in neutron and photon activation analysis"J. Radioanal. Nucl. Chem.. 239(1). 165-175 (1999)
Y. Miyamoto、H. Haba、A. Kajikawa、K. Masumoto、T. Nakanishi、K. Sakamoto:“中子和光子活化分析中的干扰”J.
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