Stability and chemical form of iodine sorbed on silver-exchanged zeolite X.
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概要
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Neutron activation technique was used to measure the amounts of I, Ag and Na elements in zeolite samples. The samples were nonradioactive before the activation analysis ; this facilitated various operations to investigate the chemical form of the sorbed iodine. It was found that the Ag<SUP>+</SUP> ions positioned in three types of sites react differently with iodine as follows : <BR>AgX•I<SUB>2n</SUB>, a physical adsorption product, released iodine immediately upon contact with water. (AgI)<SUP>+</SUP> having a strong chemical bond did not release iodine either by heating or by submerging. (Ag …I)<SUP>+</SUP> has a bond dissociation energy of several kcal•mol<SUP>-1</SUP>. When the sample was placed under water, part of the (Ag …I)<SUP>+</SUP> ions released iodine very slowly and the remainder changed to thermally stable (AgI)<SUP>+</SUP> ions. Ion-exchange reaction with aqueous sodium nitrate solution converted all of the (Ag …I)<SUP>+</SUP> ions into stable AgI product. The Ag (3)<SUP>+</SUP> ions reside in the inaccessible site for I atoms. The ratio of the populations was determined as :Ag(1)<SUP>+</SUP> : Ag (2)<SUP>+</SUP> : Ag (3)<SUP>+</SUP>= 0.33 : 0.51 : 0.16.
- 一般社団法人 日本原子力学会の論文
著者
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Matsuoka Shingo
Nuclear Engineering Research Laboratory, Faculty of Engineering, University of Tokyo
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Nakamura Hirone
Nuclear Engineering Research Laboratory, Faculty of Engineering, University of Tokyo
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Tamura Takaaki
Nuclear Engineering Research Laboratory, Faculty of Engineering, University of Tokyo
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ITO Yasuo
Tokai Division, Research Center for Nuclear Science and Technology, University of Tokyo
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TAKANO Takemi
Tokai Division, Research Center for Nuclear Science and Technology, University of Tokyo
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