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相对速率法测氯原子与一系列低碳醇的反应速率常数 总被引:2,自引:3,他引:2
在 2 92± 1K温度和 1 0 1× 10 5Pa压力下 ,以丙烷为参照物 ,采用相对速率方法测定了一系列醇与氯原子在气相中的反应速率常数 ,这些醇与氯的反应速率常数分别为 (单位 :10 7m3·mol-1·s-1) :甲醇k1=3 2 9,乙醇k2 =6 14,正丙醇k3=8 97,异丙醇k4 =4 0 0 ,正丁醇k5=11 7,异丁醇k6=12 5 ,叔丁醇k7=2 0 5 ,正戊醇k8=15 8,异戊醇k9=12 3 相似文献
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Characterization of plutonium in deep-sea sediments of the Sulu and South China Seas 总被引:1,自引:0,他引:1
Wei Dong Jian Zheng Qiuju Guo Shaoming Pan 《Journal of environmental radioactivity》2010,101(8):622-1899
Anthropogenic Pu isotopes are important geochemical tracers for sediment studies. Their distributions and sources in the water columns as well as the sediments of the North Pacific have been intensively studied; however, information about Pu in the Southeast Asian seas is limited. To study the isotopic composition of Pu, and thus to identify its sources, we collected sediment core samples in the South China Sea and the Sulu Sea during the KH-96-5 Cruise of the R/V Hakuho Maru. We analysed the activities of 239+240Pu and the atom ratios of 240Pu/239Pu using isotope dilution sector-field inductively coupled plasma mass spectrometry (SF-ICP-MS). The 240Pu/239Pu atom ratios in the sediments of both areas (inventory weighted mean: 0.251 for the South China Sea and 0.280 for the Sulu Sea) were higher than the global fallout value (0.178 ± 0.019), suggesting the existence of Pu from the Pacific Proving Grounds in the North Pacific. Low inventories of 239+240Pu in sediments were observed in the South China Sea (3.75 Bq/m2) and the Sulu Sea (1.38 Bq/m2). Most of the Pu input is still present in the water column. Scavenging and benthic mixing processes were considered to be the main processes controlling the distribution of Pu in the deep-sea sediments of both study areas. 相似文献
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Oikawa S Watabe T Inatomi N Isoyama N Misonoo J Suzuki C Nakahara M Nakamura R Morizono S Fujii S Hara T Kido K 《Journal of environmental radioactivity》2011,102(3):302-310
A radioactivity survey was launched in 1991 to determine the background levels of 239+240Pu in the marine environment off a commercial spent nuclear fuel reprocessing plant before full operation of the facility. Particular attention was focused on the 240Pu/239Pu atom ratio in seawater and bottom sediment to identify the origins of Pu isotopes. The concentration of 239+240Pu was almost uniform in surface water, decreasing slowly over time. Conversely, the 239+240Pu concentration varied markedly in the bottom water and was dependent upon the sampling point, with higher concentrations of 239+240Pu observed in the bottom water sample at sampling points having greater depth. The 240Pu/239Pu atom ratio in the seawater and sediment samples was higher than that of global fallout Pu, and comparable with the data in the other sea area around Japan which has likely been affected by close-in fallout Pu originating from the Pacific Proving Grounds. The 240Pu/239Pu atom ratio in bottom sediment samples decreased with sea depth. The land-originated Pu is not considered as the reason of the increasing 239+240Pu concentration and also decreasing the 240Pu/239Pu atom ratio with sea depth, and further study is required to clarify it. 相似文献
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S.M. Pan S.G. TimsX.Y. Liu L.K. Fifield 《Journal of environmental radioactivity》2011,102(10):930-936
A sediment core collected from the sub-aqueous delta of the Yangtze River estuary was subjected to analyses of 137Cs and plutonium (Pu) isotopes. The 137Cs was measured using γ-spectrometry at the laboratories at the Nanjing University and Pu isotopes were determined with Accelerator Mass Spectrometry (AMS), measurements made at the Australian National University. The results show considerable structure in the depth concentration profiles of the 137Cs and 239+240Pu. The shape of the vertical 137Cs distribution in the sediment core was similar to that of the Pu. The maximum 137Cs and 239+240Pu concentrations were 16.21 ± 0.95 mBq/g and 0.716 ± 0.030 mBq/g, respectively, and appear at same depth. The average 240Pu/239Pu atom ratio was 0.238 ± 0.007 in the sediment core, slightly higher than the average global fallout value. The changes in the 240Pu/239Pu atom ratios in the sediment core indicate the presence of at least two different Pu sources, i.e., global fallout and another source, most likely close-in fallout from the Pacific Proving Grounds (PPG) in the Marshall Islands, and suggest the possibility that Pu isotopes are useful as a geochronological tool for coastal sediment studies. The 137Cs and 239+240Pu inventories were estimated to be 7100 ± 1200 Bq/m2 and 407 ± 27 Bq/m2, respectively. Approximately 40% of the 239+240Pu inventory originated from the PPG close-in fallout and about 50% has derived from land-origin global fallout transported to the estuary by the river. This study confirms that AMS is a useful tool to measure 240Pu/239Pu atom ratio and can provide valuable information on sedimentary processes in the coastal environment. 相似文献
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原子吸收光谱分析通常用来测定微量元素,目前常采用石墨炉原子吸收法测定试液中ppb级或更低的痕量和超痕量元素,因此对实验过程中的污染防治就显得尤为重要.文章阐述了在原子吸收光谱测定微量元素的过程中,实验环境、水和试剂的纯度、器皿清洁度、气体(包括燃气、助燃气和惰性保护气体)的纯度以及原子化器等诸多因素均会对测定结果的准确性产生影响.对以上影响因素逐一分析并提出改进建议,以减少分析误差提高测试准确性. 相似文献
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本文总结了影响有机化合物沸点的主要因素, 详细地概括了沸点与有机物质结构的关系.尤其是在此基础上找到一种估算沸点的方法,并给出了估算式:Tb=Km·e(W/M). 利用该式,可以更准确地计算出许多有机物质的沸点. 相似文献