Method for solidifying radioactive waste comprising boron, and solid radioactive waste formed thereby

Abstract

The present invention relates to a method solidifying radioactive waste containing boron, The method includes (a) mixing the radioactive waste, metakaolin, fumed silica, potassium hydroxide, and water to generate a second mixture, in which the radioactive waste contains boron.

Claims

1. A method of solidifying radioactive waste, comprising: (a) mixing the radioactive waste, metakaolin, fumed silica, potassium hydroxide, and water to generate a second mixture; wherein the radioactive waste contains boron, and wherein a part by weight of boron is 60 or more and a part by weight of sodium is 10 or more based on 100 parts by weight of the radioactive waste.

2. The method of claim 1, wherein the (a) includes: (a-1) mixing the radioactive waste, the fumed silica, the potassium hydroxide, and the water to generate a first mixture; and (a-2) after the (a-1), mixing the metakaolin with the first mixture to generate the second mixture.

3. The method of claim 2, wherein the (a-2) proceeds after the first mixture generated in the (a-1) is stirred for 10 to 14 hours.

4. The method of claim 1, wherein a part by weight of the radioactive waste is 8 to 15 based on 100 parts by weight of the second mixture.

5. The method of claim 1, wherein a part by weight of the metakaolin is 26 to 31 based on 100 parts by weight of the second mixture.

6. The method of claim 1, wherein a part by weight of the potassium hydroxide is 18 to 21 based on 100 parts by weight of the second mixture.

7. The method of claim 1, wherein a part by weight of the fumed silica is 14 to 16 based on 100 parts by weight of the second mixture.

8. The method of claim 1, wherein a part by weight of the water is 24 to 27 based on 100 parts by weight of the second mixture, and the water is deionized water.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a diagram schematically illustrating a method of solidifying radioactive waste according to the present invention.

(2) FIG. 2 is a diagram illustrating a compressive strength of a solidified radioactive waste prepared according to a weight ratio of each chemical composition in the method of solidifying radioactive waste according to the present invention.

(3) FIG. 3 is a result of 11B solid-state nuclear magnetic resonance analysis of a solidified radioactive waste prepared by the method of solidifying radioactive waste according to the present invention.

BEST MODE

(4) Hereinafter, a method according to the present disclosure will be described in detail with reference to the accompanying drawings. In this process, thicknesses of lines, sizes of components, and the like, illustrated in the accompanying drawings may be exaggerated for clearness of explanation and convenience. In addition, terms to be described below are defined in consideration of functions in the present disclosure and may be construed in different ways by the intention of users or practice. Therefore, these terms should be defined on the basis of the contents throughout the present specification.

(5) Referring to FIG. 1, a method of solidifying radioactive waste for solidifying radioactive waste containing boron will be described.

(6) In the present invention, the solidified radioactive waste refers to being solidified in a state in which a solidifying material and radioactive waste are mixed. The present invention is to propose a method of preparing a solidified radioactive waste using metakaolin-based geopolymer.

(7) The solidified radioactive waste was prepared using radioactive waste containing boron, deionized water (DWI), sodium hydroxide (NaOH), and fumed silica were used or using radioactive waste containing boron, deionized water (DWI), potassium hydroxide (KOH), and fumed silica.

(8) The radioactive waste according to the present invention may be concentrated liquid waste in a powder form in which liquid waste containing boron as liquid waste generated from a reactor is concentrated and dried.

(9) The metakaolin according to the present invention may be metakaolin having a main component of amorphous aluminosilicate and having 1% or less of calcium.

(10) TABLE-US-00001 TABLE 1 Molar ratio of Parts by weight of Molar ration of chemical composition of solidified radioactive waste Si/(Al + B) radioactive waste Solidified radioactive waste using Na.sub.2O:(B.sub.2O.sub.3 + Al.sub.2O.sub.3):3.0SiO.sub.2:9H.sub.2O 1.5 10 sodium hydroxide alkali activator Na.sub.2O:(B.sub.2O.sub.3 + Al.sub.2O.sub.3):2.8SiO.sub.2:9H.sub.2O 1.4 12 Na.sub.2O:(B.sub.2O.sub.3 + Al.sub.2O.sub.3):2.6SiO.sub.2:9H.sub.2O 1.3 15 Solidified radioactive waste using (Na.sub.2O + K.sub.2O):(B.sub.2O.sub.3 + Al.sub.2O.sub.3):3.0SiO.sub.2:9H.sub.2O 1.5 9 potassium hydroxide alkali activator (Na.sub.2O + K.sub.2O):(B.sub.2O.sub.3 + Al.sub.2O.sub.3):2.8SiO.sub.2:9H.sub.2O 1.4 12 (Na.sub.2O + K.sub.2O):(B.sub.2O.sub.3 + Al.sub.2O.sub.3):2.6SiO.sub.2:9H.sub.2O 1.3 14

(11) TABLE-US-00002 TABLE 2 Si/(Al + B) 1.5 Si/(Al + B) 1.4 Si/(Al + B) 1.3 Feedstock g wt % Feedstock g wt % Feedstock g wt % MK 55.08 32.40% MK 52.04 30.61% MK 50.94 28.30% Waste 17.03 10.02% Waste 20.94 12.32% Waste 27.07 15.04% Fumed silica 28.71 16.89% Fumed silica 27.20 16.00% Fumed silica 27.56 15.31% NaOH 23.24 13.67% NaOH 23.17 13.63% NaOH 24.32 13.51% Water 45.93 27.02% Water 46.65 27.44% Water 50.11 27.84% Total 170.00 100.00% Total 170.00 100.00% Total 180.00 100.00% MK 54.11 30.06% MK 50.63 28.13% MK 48.37 26.87% Waste 16.76 9.31% Waste 21.01 11.67% Waste 25.09 13.94% Fumed silica 28.22 15.68% Fumed silica 26.82 14.90% Fumed silica 25.51 14.17% KOH 36.20 20.11% KOH 36.14 20.08% KOH 33.89 18.83% Water 44.71 24.84% Water 45.40 25.22% Water 47.16 26.20% Total 180.00 100.00% Total 180.00 100.00% Total 180.00 100.01%

(12) TABLE-US-00003 TABLE 3 Si(Al + B) 1.5 Feedstock g wt % MK 56.67 31.47% Waste 18.00 10.00% Fumed silica 29.66 16.48% KOH 51.05 28.36% Water 24.62 13.699% Total 180.00 100.00%

(13) Table 1 shows the molar ratio of the chemical composition of the solidified radioactive waste prepared according to each case of Table 2, which shows a weight ratio of a chemical composition, and a weight ratio of the radioactive waste to a total weight of the solidified radioactive waste.

(14) Table 2 shows the weight ratio of the chemical composition used to prepare the solidified radioactive waste corresponding to the Si/(Al+B) ratio in Table 1.

(15) Table 3 for comparing the effect on the compressive strength of the solidified radioactive waste according to the weight ratio of the chemical composition shows the weight ratio of the chemical composition used to prepare the solidified radioactive waste with a Si/(Al+B) ratio of 1.5. The weight ratio of the chemical composition in Table 3 is a weight ratio with a certain degree of difference from the weight ratio of the chemical composition in Table 2 in that range.

(16) 1. Preparation of Alkali Activator

(17) Preferentially, a sodium hydroxide alkali activator was prepared by mixing deionized water, sodium hydroxide (NaOH), and fumed silica so that the chemical composition of the solidified radioactive waste prepared was as shown in Table 1. In addition, a potassium hydroxide alkali activator was prepared by mixing deionized water, potassium hydroxide (KOH), and fumed silica so that the chemical composition of the solidified radioactive waste prepared was as shown in Table 1.

(18) Furthermore, the alkali activators corresponding to the weight ratios in Table 3 were prepared.

(19) 2. Preparation of First Mixture and Third Mixture

(20) Thereafter, the radioactive waste containing boron was added to each potassium hydroxide alkali activator so that the chemical composition of the prepared solidified radioactive waste was as shown in Table 1 to generate a first mixture, and then the first mixture was stirred at 25 C. for about 12 hours.

(21) Similarly, the radioactive waste containing boron was added to each sodium hydroxide alkali activator so that the chemical composition of the prepared solidified radioactive waste was as shown in Table 1 to generate a third mixture, and then the third mixture was stirred at 25 C. for about 12 hours.

(22) Similarly, the radioactive waste containing boron was added to the sodium hydroxide alkali activator in the weight ratio of Table 3 to generate a mixture, and then the mixture was stirred at 25 C. for about 12 hours.

(23) The radioactive waste used in the experiment is simulated radioactive waste prepared by mixing reagents in accordance with the component ratio of actual radioactive waste.

(24) 3. Preparation of Second Mixture and Fourth Mixture

(25) Next, the metakaolin was added to the potassium hydroxide alkali activator containing radioactive waste containing boron so that the chemical composition of the prepared solidified radioactive waste was as shown in Table 1 to generate a second mixture, and then a centrifugal mixer was used to stir the second mixture at 1800 RPM for about 2 minutes.

(26) Similarly, the metakaolin was added to the sodium hydroxide alkali activator containing radioactive waste containing boron so that the chemical composition of the prepared solidified radioactive waste was as shown in Table 1 to generate a fourth mixture, and then a centrifugal mixer was used to stir the fourth mixture at 1800 RPM for about 2 minutes.

(27) Similarly, the metakaolin is added to the sodium hydroxide alkali activator containing the radioactive waste containing boron in the weight ratio of Table 3 to generate a mixture, and then the centrifugal mixer was used to stir the fourth mixture at 1800 RPM for about 2 minutes.

(28) 4. Curing

(29) Next, the second mixture and the fourth mixture were poured into a cylindrical mold having a diameter and ratio of 1:2. Thereafter, the second mixture and the fourth mixture were cured in an oven maintained at 60 C. for 6 days and then stored at room temperature for 1 day. Thereafter, compressive strength was measured after 7 days of age.

(30) The same applies to the mixture generated by adding the metakaolin to the sodium hydroxide alkali activator containing the radioactive waste containing boron in the weight ratio of Table 3.

(31) The weight ratio will be described.

(32) In Table 2, Si/(Al+B) represents the mole of silicon to the mole obtained by summing the mole of boron and the mole of aluminum in the prepared solidified radioactive waste shown in Table 1.

(33) In Table 3, Si/(Al+B) represents the mole of silicon to the mole obtained by summing the mole of boron and the mole of aluminum in the solidified radioactive waste prepared according to the weight ratio of Table 3.

(34) As it is known that the content of silicon in the solidified radioactive waste has a great effect on the mechanical properties (including the compressive strength) of the solidified radioactive waste form, this is to review the compressive strength according to the case where the molar ratio of silicon may be changed based on the mole obtained by summing the mole of boron and the mole of aluminum.

(35) In Table 1, sodium (Na) in the solidified radioactive waste using the potassium hydroxide alkali activator is sodium contained in the radioactive waste, not the alkali activator.

(36) Further, the molar ratio of water to the mole obtained by summing the mole of boron and the mole of aluminum may be 9.

(37) In addition, Table 2 shows the weight ratio of the chemical composition in the second mixture for preparing the solidified radioactive waste using the potassium hydroxide alkali activator and the weight ratio of the chemical composition in the fourth mixture for preparing the solidified radioactive waste using the sodium hydroxide alkali activator, in preparing each solidified radioactive waste.

(38) The weight ratio of the solidified radioactive waste using the potassium hydroxide alkali activator is as follows.

(39) The content of boron in the radioactive waste used may be 60 parts by weight or more based on 100 parts by weight of the radioactive waste, and the content of sodium in the radioactive waste used may be 10 parts by weight or more based on 100 parts by weight of the radioactive waste.

(40) Preferably, a part by weight of the radioactive waste containing boron may be 8 to 15 based on 100 parts by weight of the second mixture.

(41) Preferably, a part by weight of the metakaolin may be 26 to 31 based on 100 parts by weight of the second mixture.

(42) Preferably, a part by weight of the potassium hydroxide may be 18 to 21 based on 100 parts by weight of the second mixture.

(43) Preferably, a part by weight of the fumed silica may be 14 to 16 based on 100 parts by weight of the second mixture.

(44) Preferably, a part by weight of water is 24 to 27 based on 100 parts by weight of the second mixture, and as described above, water may be deionized water.

(45) The weight ratio of the solidified radioactive waste using the sodium hydroxide alkali activator is as follows.

(46) The content of boron in the radioactive waste used may be 60 parts by weight or more based on 100 parts by weight of the radioactive waste, and the content of sodium in the radioactive waste used may be 10 parts by weight or more based on 100 parts by weight of the radioactive waste.

(47) Preferably, a part by weight of the radioactive waste containing boron may be 9 to 16 based on 100 parts by weight of the fourth mixture.

(48) Preferably, a part by weight of the metakaolin may be 28 to 33 based on 100 parts by weight of the fourth mixture.

(49) Preferably, a part by weight of the sodium hydroxide may be 13 to 14 based on 100 parts by weight of the fourth mixture.

(50) Preferably, a part by weight of the fumed silica may be 15 to 17 based on 100 parts by weight of the fourth mixture.

(51) Preferably, a part by weight of water is 27 to 28 based on 100 parts by weight of the fourth mixture, and as described above, water may be deionized water.

(52) The weight ratio of the solidified radioactive waste to compare the effect on the compressive strength of the solidified radioactive waste form according to the weight ratio is shown in Table 3. Similarly, the content of boron in the radioactive waste used may be 60 parts by weight or more based on 100 parts by weight of the radioactive waste and the content of sodium in the radioactive waste used may be 10 or more parts by weight based on 100 parts by weight of the radioactive waste.

(53) Referring to FIG. 2, the compressive strength of each solidified radioactive waste will be described.

(54) As described above, the compressive strength is the compressive strength after 7 days of age after pouring the second mixture and the fourth mixture into the cylindrical mold having a diameter and ratio of 1:2, curing the mixtures in an oven maintained at 60 C. for 6 days, and then storing the mixtures at room temperature for 1 day. The same goes for the mixture according to the weight ratio of Table 3.

(55) In order to compare the compressive strength of solidified radioactive waste using the potassium hydroxide alkali activator and the compressive strength of solidified radioactive waste using the potassium hydroxide alkali activator, as shown in Table 1, the molar ratio of the aluminum and boron to the sodium in the solidified radioactive waste using the sodium hydroxide alkali activator was the same as the molar ratio of the aluminum and boron to the potassium in the solidified radioactive waste using the potassium hydroxide alkali activator.

(56) The compressive strength of the solidified radioactive waste using the potassium hydroxide alkali activator was generally higher than that of the solidified radioactive waste using the sodium hydroxide alkali activator. Therefore, it can be seen that the solidified radioactive waste using the potassium hydroxide is more suitable than the case of using the sodium hydroxide as the alkali activator.

(57) The compressive strength of the metakaolin-based geopolymer increases in proportion to the silicon content up to a specific silicon/aluminum ratio (1.9 to 2.1), which is known to be due to an increase in the SiOSi bond ratio.

(58) It has been known that potassium, which has a larger ion size than sodium, is bonded with silicate oligomer with a long molecular chain to increase the connectivity of microstructures, thereby having a positive effect on the compressive strength.

(59) Additionally, in the case of the solidified radioactive waste prepared according to the weight ratio of Table 3, the compressive strength is shown as 0.

(60) That is, as it can be seen that there is a significant difference between the compressive strength of the solidified radioactive waste using the potassium hydroxide alkali activator according to Table 2 and the compressive strength of the solidified radioactive waste prepared according to Table 3, it can be seen that the compressive strength of the prepared solidified radioactive waste is changed depending on the weight ratio of the chemical composition.

(61) In the case of the weight ratio of Table 3, the compressive strength is 0, indicating a state in which the solidified radioactive waste is not formed because the radioactive waste is not solidified. That is, in the case of the radioactive waste containing boron, when prepared within a certain range of weight ratios including the weight ratios of Table 3, it can be seen that the solidified radioactive waste is not generated because the radioactive waste is not solidified.

(62) Referring to FIG. 3, the bonding structure of the boron and silicon included in the solidified radioactive waste will be described.

(63) Regardless of the type of alkali activator, a .sup.4B (1B, 3Si) peak indicating boron and silicon bonding was found in all the solidified radioactive wastes, which means that boron, the main component of the radioactive waste, was bonded by substituting silicon in the geopolymer structure.

(64) Hereinabove, the present specification has been described with reference to the embodiments illustrated in the drawings so that those skilled in the art can easily understand and reproduce the present invention, but this is only exemplary, and those skilled in n the art will understood that other embodiments equivalents variously modified from and equivalent to the embodiments of the present invention are possible. Therefore, the scope of protection of the present invention should be defined by the claims.