Amorphous inorganic anion exchanger, resin composition for electronic component sealing, and process for producing amorphous bismuth compound
US-2015321189-A1 · Nov 12, 2015 · US
US2016361701A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016361701-A1 |
| Application number | US-201414580628-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 23, 2014 |
| Priority date | Dec 24, 2013 |
| Publication date | Dec 15, 2016 |
| Grant date | — |
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Provided are an adsorbent for trapping a radioactive iodine gas generated in a process of oxidizing a nuclear fuel at a high temperature after use and a method of preparing the same, and more particularly, a radioactive iodine gas adsorbent which is formed of bismuth as a main component, thereby exhibiting an excellent radioactive iodine gas trapping capability and an excellent thermal stability after trapping, and a method of preparing the same. An adsorbent for trapping a radioactive iodine gas prepared by a method of preparing an adsorbent for trapping a radioactive iodine gas according to the present disclosure may effectively trap a radioactive iodine off-gas generated in a nuclear fuel pre-treated oxidizing process after use. Particularly, the adsorbent may trap iodine in a larger amount, which is twice or more, than a silver-containing zeolite widely used to trap a radioactive iodine gas, and the trapped iodine forms a stable compound, which is more advantageous for long-term storage. In addition, since an iodine gas is trapped using inexpensive bismuth, instead of expensive silver, in consideration of trapping a large amount of a radioactive iodine gas, the adsorbent has very excellent economic feasibility.
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What is claimed is: 1 . A method of manufacturing a radioactive iodine gas adsorbent, comprising the following steps of: (a) preparing a mixed solution by mixing a solution including 10 to 20 wt % of bismuth nitrate and a solution including 10 to 20 wt % of polyvinylalcohol; (b) preparing a mixture by drying the mixed solution to remove moisture; (c) preparing an oxide by heat-treating the mixture in an atmospheric ambience to remove the polyvinylalcohol; and (d) reducing the oxide to a bismuth element state by heat-treating the oxide in a hydrogen ambience. 2 . The method according to claim 1 , wherein, in the step (a), the solution including 10 to 20 wt % of bismuth nitrate includes 10 to 50 ml of nitric acid per 100 ml of distilled water. 3 . The method according to claim 1 , wherein the drying in the step (b) is performed at 40 to 70° C. for 1 to 4 days. 4 . The method according to claim 1 , wherein the thermal treatment in the step (c) is performed in an atmospheric ambience at 400 to 500° C. for 2 to 3 hours. 5 . The method according to claim 1 , wherein the reduction in the step (d) is performed in a 4% hydrogen ambience at 300 to 350° C. for 6 to 12 hours. 6 . A radioactive iodine gas adsorbent manufactured by the manufacturing method according to claim 1 . 7 . The adsorbent according to claim 6 , wherein the adsorbent is a porous. 8 . A method of trapping a radioactive iodine gas, comprising: trapping a gas containing a radioactive iodine gas by passing through the adsorbent of claim 6 . 9 . The method according to claim 8 , which is performed at 200 to 250° C. for 24 hours.
by adsorption, e.g. preparative gas chromatography {(solid sorbent compositions B01J20/00, preparation of inorganic compounds or elements C01)} · CPC title
by treating the gases with solids · CPC title
Treating gases · CPC title
comprising inorganic material · CPC title
Metals · CPC title
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