JPH0552993A - Eliminating method for radioactive iodine ion - Google Patents

Abstract

PURPOSE:To efficiently eliminate radioactive iodine ion contained in solution by stabilizing as BI5O7I single phase. CONSTITUTION:Radioactive iodine ion and bismuth oxide (alpha-Bi2O3) included in KI and LiI solutions are directly reacted by adjusting the ratio of bismuth oxide gram molecule number and iodine ion gram ion number at 4 to 1 through 1 to 4 for KI solution and 5 to 2 through 1 to 2 for LiI solution. Radioactive iodine ion is thus stabilized into alpha-Bi5O7I and more than 99% thereof is eliminated.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for removing radioactive iodine ions, which is suitable for removing iodine ions in radioactive waste liquid generated in a nuclear power plant, for example.

[0002]

2. Description of the Related Art In a nuclear power plant, radioactive iodine gas produced by nuclear fission in a nuclear reactor is suddenly released when a fuel is inspected or replaced and when a fuel handling accident or a nuclear reactor runaway accident occurs. Dangerous and can be continuously released during operation of the fuel reprocessing plant. For such various situations, as a treatment method of radioactive iodine gas, a cleaning treatment method, a physical / chemical treatment method by filling a solid adsorbent, a treatment with an ion exchange agent, and the like are being studied.

[0003]

However, in the cleaning treatment method using a liquid adsorbent, if it is stored as a liquid for a long time (half-life is 17 million years), there is a problem in terms of quantity and safety. There are many. Also, in the physical / chemical treatment method by filling the solid adsorbent, the captured iodine is always exposed to the possibility of exchange with other gas, and the adsorbate is easily released when the temperature rises. There are difficulties. Furthermore, in the treatment method using an ion exchange agent, the heat resistance stability of the exchange resin is maintained up to about 100 ° C., and at a temperature higher than this, sufficient performance is not exhibited. In addition, since it is flammable itself, there is a problem in safety management.

From such a point of view, an attempt (reaction method) of reacting radioactive iodine ions in a solution with other elements to extract them as a stable compound for storage is also being studied. In this method, bismuth oxide (α-Bi ₂ O ₃ ) is added to a NaI solution and reacted, and iodine ions in the solution are reacted with α-Bi ₅ O ₇ I.
It is to change into and take out. In this reaction, the cation (Na +) coexisting with the iodine ion also plays an important role. If α-Bi ₂ O ₃ is added to the NH ₄ I solution and reacted with iodide ions, the product is not an α-Bi ₅ O ₇ I single phase. The cause is a cation that coexists with iodine ion.

[Chemical 1] It seems to be in.

The present invention solves the problems of the prior art described above, and reacts radioactive iodine ions contained in a KI solution or a LiI solution with bismuth oxide to produce only a Bi ₅ O ₇ I single phase and immobilize it. It is an object of the present invention to provide a method that can be efficiently converted into a product.

[0006]

In order to solve the above-mentioned problems, the present inventor has found that even when a radioiodine ion is reacted with bismuth oxide, only Bi ₅ O ₇ I single phase is produced, and other compounds As a result of earnest research on the condition that does not generate,
The present invention has been completed here.

That is, according to the present invention, radioactive iodine ions and bismuth oxide (α-B) contained in KI and LiI solutions are contained.
i ₂ O ₃ ) is 4: 1 when the ratio of the number of gram molecules of bismuth oxide to the number of gram ions of iodine ions is 4: 1.
From 1: 4 to 1: 4, and in the case of LiI solution, from 5: 2 to 1: 2, the reaction is carried out directly, and the radioactive iodine ion is immobilized as α-Bi ₅ O ₇ I to be removed. It is a feature.

The present invention will be described in more detail below.

[0009]

[Action]

For bismuth oxide, α-, β-, γ-, δ-
There are polymorphs of phases, α type is a low temperature stable phase, δ phase is a high temperature stable phase, and the others are metastable phases. Bi ₅ O ₇ I also has α and β polymorphs. In the following description, Bi ₂ O ₃ and Bi ₅ O ₇ I both represent α-form compounds.

The compounds of bismuth (Bi), oxygen (O) and iodine (I) include α-Bi ₅ O ₇ I, β-Bi ₅ O ₇ I and Bi ₇ O.
Five kinds of compounds, ₉ I ₃ , Bi ₄ O ₅ I ₂ and BioI, have been reported. These have different crystal structures,
Solid at room temperature. Among these compounds, α-Bi ₅ O ₇
I is the most stable to water and heat. For example, the concentration of iodine ion that is decomposed in a non-acidic solution (25 ° C) is about 10 ^-17 mol · dm ^-3, which is extremely small. Is.
Further, it is stable up to about 550 ° C. against heating in air, and these stability are incomparably higher than those of other methods.

In the present invention, a KI solution or a LiI solution is used to react radioiodine ions in the solution with bismuth oxide (α-Bi ₂ O ₃ ) to form a Bi ₅ O ₇ I single phase. The solution is stored separately from the solution. This reaction proceeds according to the following equation.

5α-Bi ₂ O ₃ + 2I ⁻ + H ₂ O → 2α-Bi ₅ O ₇ I + 2OH ⁻ (1)

In carrying out this chemical reaction, the only product is Bi ₅ O ₇ I, and in order to prevent the formation of other compounds, the number of gram molecules of bismuth oxide involved in the reaction and the iodine ion The ratio with the number of gram ions is KI
It should be adjusted between 4: 1 and 1: 4 for solutions and between 5: 2 and 1: 2 for LiI solutions. If the proportion of iodine is higher or lower than this, compounds other than Bi ₅ O ₇ I will grow.

Further, according to the present invention, the kinds of cations coexisting with iodine ions are

[Chemical 2] not,

[Chemical 3] Or

[Chemical 4] Or even if they coexist, Bi ₅ O ₇
I Solidification by a single phase is possible. Moreover, Bi ₅ O ₇ I
The upper limit of the conditions (ratio between the number of gram molecules of bismuth oxide and the number of gram ions of iodine ions) for producing only
It is 1: 4 in the case of the I solution, which is larger than the upper limit (1: 2) in the case of the NaI solution, and the range over which Bi ₅ O ₇ I can stably grow is wider.

Next, examples of the present invention will be described.

[0017]

Example 1 About 233 mg (5 × 1) of bismuth oxide (Bi ₂ O ₃ ).
^0-4 gram molecule) and 0.2 mol · dm ^-3 of potassium iodide solution 1000 μl (2 × 10 ^-4 gram ion) are put in a container with a lid and hermetically sealed at 25 ° C and 50 ° C in a constant temperature bath. It was made to react. Do not stir. After a certain period of time, the solid was separated from the solution, dried, and then identified by a powder X-ray diffraction method. The progress of the reaction was examined by comparing this with the powder X-ray diffraction pattern of the solid (Bi ₂ O ₃ ) before the reaction. Chemical formula (1)
According to the above, when the reaction is completed, the residual amount of Bi ₂ O ₃ should be zero, and the X-ray diffraction pattern should disappear, examples of which are shown in A (before reaction) and B (after reaction) of FIG.

[Table 1] As is clear from the results shown in Table 1, the reaction rate varies slightly depending on the temperature, but at 50 ° C., the reaction is completed within 48 hours, and a Bi ₅ O ₇ I single phase is obtained. It takes more time to obtain this single phase at 25 ° C.

[0018]

Example 2 Bismuth oxide (Bi ₂ O ₃ ) about 233 mg (5 × 1)
(0 ⁻⁴ gram molecule) and 0.8 mol · dm ⁻³ of potassium iodide solution (250 μl, 2 × 10 ⁻⁴ gram ion) were reacted at 50 ° C. to examine the progress. The experimental procedure is the same as in Example 1.

[Table 2] As is clear from the results shown in the above, the reaction was completed within 24 hours, and a Bi ₅ O ₇ I single phase was obtained.

[0019]

Example 3 Approximately 233 mg of bismuth oxide (Bi ₂ O ₃ ) and 1000 μl of potassium iodide solution having various concentrations were mixed at 50 ° C. for 9 days.
The result of reacting for 6 hours

[Table 3] Shown in. It can be seen that Bi ₅ O ₇ I single phase is obtained under conditions within the scope of the present invention.

[0020]

Example 4 About 233 mg of bismuth oxide (Bi ₂ O ₃ ) and 250 μl of potassium iodide solution having various concentrations were added at 50 ° C. for 48 hours.
The result of the reaction

[Table 4] Shown in. It can be seen that Bi ₅ O ₇ I single phase is obtained under conditions within the scope of the present invention.

[0021]

Example 5 About 233 mg of bismuth oxide (Bi ₂ O ₃ ) and 1000 μl of a lithium iodide solution having various concentrations were mixed at 50 ° C. for 9 hours.
The result of reacting for 6

[Table 5] Shown in. It can be seen that Bi ₅ O ₇ I single phase is obtained under conditions within the scope of the present invention.

[0022]

Example 6 To examine the reaction rate of iodine ions, about 255 mg (5.5 × 10 ⁻⁴ gram molecule) of bismuth oxide (Bi ₂ O ₃ ) and 0.2 mol · dm ⁻³ potassium iodide solution and After reacting 1000 μl (2 × 10 ⁻⁴ gram ion) of the iodium iodide solution at 50 ° C. for 72 hours, the concentration of the iodine ion remaining in the solution was analyzed. As a result, the concentration of iodine ions remaining after the reaction was 0.32% of the concentration of the solution before the reaction in the case of the KI solution, and 0.23% of the concentration of the solution before the reaction in the case of the LiI solution. .. All other iodine ions are considered to have changed to solids.

As is clear from the results of Examples 1 and 2,
When the volume ratio of the raw material solid to the reaction solution is changed, the reaction rate also changes. The reaction rate slows as the volume of the solution increases.
In addition, as is clear from the results of Examples 3, 4, and 5, B
It was confirmed that the condition necessary for producing only i ₅ O ₇ I was to keep the ratio of the number of gram molecules of Bi ₂ O _{3 to} the number of gram ions of I ⁻ within a certain range.

[0024]

As described above, according to the present invention, radioactive iodine ions present in a solution can be reacted with bismuth oxide to take out only Bi ₅ O ₇ I simple phase, and 99% or more can be taken out. It can be removed as a solid. Further, the stability against water, heat and various gases is remarkably improved. Moreover, since this compound is a solid crystal, it is not bulky in quantity and is easy to store and handle.

[Brief description of drawings]

FIG. 1 is a diagram showing a powder X-ray diffraction pattern, in which A is a raw material.
In the case of (Bi ₂ O ₃ ), B is the case where the product is Bi ₅ O ₇ I only.

Claims (1)

[Claims] 1. A radioactive iodine ion contained in a KI and LiI solution and bismuth oxide (α-Bi ₂ O ₃ ) are contained in a KI solution having a ratio of the gram molecular number of bismuth oxide to the gram ion number of iodine ion. In some cases between 4: 1 and 1: 4,
In the case of LiI solution, it is adjusted between 5: 2 and 1: 2 for direct reaction, and radioiodine ion is immobilized and removed as α-Bi ₅ O ₇ I to remove radioiodine ion. Method.