EP0773555A1 - Neutron-shielding hydraulic hardening material and method of manufacturing neutron shields using the same - Google Patents
Neutron-shielding hydraulic hardening material and method of manufacturing neutron shields using the same Download PDFInfo
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- EP0773555A1 EP0773555A1 EP96118207A EP96118207A EP0773555A1 EP 0773555 A1 EP0773555 A1 EP 0773555A1 EP 96118207 A EP96118207 A EP 96118207A EP 96118207 A EP96118207 A EP 96118207A EP 0773555 A1 EP0773555 A1 EP 0773555A1
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- weight
- neutron
- shielding
- hardening material
- entraining
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- 239000000463 material Substances 0.000 title claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 46
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 18
- 229910052580 B4C Inorganic materials 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 239000011396 hydraulic cement Substances 0.000 claims abstract description 10
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 9
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000126 substance Substances 0.000 claims abstract description 6
- 239000004088 foaming agent Substances 0.000 claims abstract description 5
- 239000004014 plasticizer Substances 0.000 claims abstract description 4
- 238000004898 kneading Methods 0.000 claims abstract description 3
- 239000011369 resultant mixture Substances 0.000 claims abstract description 3
- 239000002245 particle Substances 0.000 claims description 19
- 238000010079 rubber tapping Methods 0.000 claims description 6
- 238000009415 formwork Methods 0.000 claims description 5
- 239000004570 mortar (masonry) Substances 0.000 abstract description 18
- 230000000694 effects Effects 0.000 abstract description 5
- 238000000034 method Methods 0.000 abstract description 5
- 239000000843 powder Substances 0.000 description 17
- 239000004568 cement Substances 0.000 description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 11
- 229910052796 boron Inorganic materials 0.000 description 11
- 239000000654 additive Substances 0.000 description 7
- 239000011148 porous material Substances 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 238000009826 distribution Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000011398 Portland cement Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 239000003758 nuclear fuel Substances 0.000 description 4
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 3
- 229910001679 gibbsite Inorganic materials 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 229910052810 boron oxide Inorganic materials 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000011402 Portland pozzolan cement Substances 0.000 description 1
- 239000011401 Portland-fly ash cement Substances 0.000 description 1
- 239000011400 blast furnace cement Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910021540 colemanite Inorganic materials 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 229910001648 diaspore Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000002927 high level radioactive waste Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000012958 reprocessing Methods 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002915 spent fuel radioactive waste Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21F—PROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
- G21F1/00—Shielding characterised by the composition of the materials
- G21F1/02—Selection of uniform shielding materials
- G21F1/04—Concretes; Other hydraulic hardening materials
- G21F1/042—Concretes combined with other materials dispersed in the carrier
Definitions
- the present invention relates to a neutron-shielding material which is useful in the fields of nuclear power plants, reprocessing of spent nuclear fuels, spent nuclear fuel disposal, medicine, etc., and particularly useful for shielding neutrons generated from various sources in such fields.
- the invention also relates to a method of manufacturing neutron shields.
- the energetic neutrons be slowed down to thermal neutrons using elements having a small atomic mass number, e.g., hydrogen (H), and that the thermal neutrons be absorbed by a suitable substance such as boron (B).
- H hydrogen
- B boron
- Cement is a relatively good material for shielding neutrons because, when transformed into mortar or concrete, it is mixed with water so as to form a hydrate that traps water therein.
- the amount of water bound as a constituent of hydrate is small, and the greater part of mixed water is free water, which is likely to be lost due to evaporation, etc.
- Plastics such as polyethylene may also contain a relatively large amount of hydrogen.
- plastics are weak against heat and have poor long-term durability. In addition, they are difficult to form into large members of high density. For these reasons, uses of plastics are limited.
- Exemplary substances containing boron include natural minerals such as colemanite (2CaO ⁇ 3B 2 O 3 ⁇ 5H 2 O) and kurnakovite (2MgO ⁇ 3B 2 O 3 ⁇ 13H 2 O).
- these minerals In order to shield neutrons, use of these minerals as aggregate of concrete may be conceivable.
- the boron content in these minerals is as low as 12-17% by weight, so it is difficult to secure boron content at a high concentration.
- these minerals release B 2 O 3 , which inhibits cement from setting or hardening.
- To suppress release of B 2 O 3 there has been made an attempt to coarsen the grain size of aggregate to thereby reduce specific surface area. This approach, however, cannot avoid uneven distribution of boron in concrete.
- control of grain size of powdery aggregate is difficult. As a result, it is not only impossible to obtain highly plasticized concrete, but it also becomes difficult to place concrete into a formwork uniformly.
- conventional neutron shields and materials therefor have the following drawbacks: Limited hydrogen content and boron content; low strength against heat and external physical force; a tendency to leave large voids in concrete products; difficulty in forming large members or members having complex shapes; and difficulty in obtaining shields having a uniform composition. Therefore, they are not satisfactory as neutron shields around nuclear reactors or high level radioactive waste.
- hydraulic hardening materials containing hydraulic cement, aluminum hydroxide, and boron carbide at certain proportions have excellent neutron shielding properties, strength of afterhardening products, and workability of fresh mortar, and that they are capable of forming uniform shields.
- the present invention was accomplished based on these findings.
- the present invention provides a hydraulic hardening material for shielding neutrons (hereinafter may be referred to as neutron-shielding material) characterized by containing 10-50% by weight of hydraulic cement, 30-88% by weight of aluminum hydroxide, and 0.1-35% by weight of boron carbide.
- the present invention also provides a method of manufacturing a neutron shield including the steps of mixing 100 parts by weight of the above-mentioned neutron-shielding hydraulic hardening material, 15-50 parts by weight of water, and not more than 5 parts by weight of at least one chemical admixture selected from the group consisting of air-entraining (AE) agents, air-entraining and water reducing agents, high-range water reducing agents, plasticizers, air-entraining and high-range water reducing agents, and foaming agents; and kneading the resultant mixture.
- AE air-entraining
- the hydraulic cement provides the target afterhardening structure with strength when mixed with water
- aluminum hydroxide provides hydrogen atoms that slow down highly energetic neutrons to thermal neutrons
- boron carbide provides boron atoms that absorb thermal neutrons which have been slowed down by hydrogen atoms.
- Hydraulic cements are not particularly limited so far as they harden when mixed with water to thereby develop strength.
- they may be any one of Portland cements such as ordinary Portland cement and high-early-strength Portland cement; blended cements such as Portland blast-furnace slag cement, Portland pozzolan cement, and Portland fly-ash cement; or ultra-rapid-hardening cement (Jet cement).
- Portland cements such as ordinary Portland cement and high-early-strength Portland cement
- blended cements such as Portland blast-furnace slag cement, Portland pozzolan cement, and Portland fly-ash cement
- ultra-rapid-hardening cement Jet cement
- admixtures such as blast-furnace slag, silica fume, fly ash, limestone powder, and gypsum.
- additives that are ordinarily used in mortar and concrete; e.g., expansive additives, accelerator, corrosion inhibitor, and waterproofing agents.
- Aluminum hydroxide may take a polymorphism such as diaspore, boemite, and gibbsite. In consideration of stability at high temperatures, gibbsite is most preferred. The theoretical hydrogen content of gibbsite is 3.8% by weight.
- B 4 C Boron carbides take the form of B 4 C, B 8 C, B 13 C 2 , etc. Under general circumstances, B 4 C is the easiest one to obtain. Moreover, B 4 C is preferred because of its good stability. The theoretical boron content of B 4 C is as high as 78% by weight.
- hydraulic cement When a neutron-shielding hydraulic hardening material neutrons is mixed with water and thereby hardens to develop enough strength as a structure, it is necessary that hydraulic cement be present in the amount of at least 10% by weight. If hydrogen and boron are both co-present, the neutron absorbing effect may be exerted more effectively. Therefore, it is concluded that proper ranges for the content of hydraulic cement, aluminum hydroxide, and boron carbide are 10-50% by weight, 30-88% by weight, and 0.1-35% by weight, respectively.
- Hydraulic cement is obtained through grinding the clinker that has been burned in a rotary kiln, and mixing it with suitable admixtures such as gypsum.
- Aluminum hydroxide is usually manufactured using a Bayer's process for industrial production.
- Boron carbide is normally manufactured through carbonizing of boron oxide (B 2 O 3 ) using carbon, and the resultant mass is used after being pulverized.
- hydraulic hardening materials obtained by the mixture of these heterogeneous powders have poor fluidity when mixed with water. In extreme cases, flow and slump are barely obtainable.
- ordinary tamping bars cannot achieve uniform filling of the cement into a flow cone or a slump cone; therefore a vibrator is usually required for achieving a uniform placing.
- the powder in a dry state preferably has a filling ratio of not lower than a threshold value.
- the filling rate be not less than 55%, more preferably not less than 60%, when measured in such a manner that the powder in a dry state is put in a hollow cylindrical container having an inner diameter of 5 cm and a height of 5 cm, and then compacted by 180 tappings from the height of 2 cm.
- the particles when sieved through a mesh of 1 mm, be of such distribution that oversize particles are present in an amount of not more than 5% by weight, particles having a diameter of equal to or smaller than 100 ⁇ m are present in an amount of 60-80% by weight, and particles having a diameter of 60-90 ⁇ m are present in an amount of not more than 20% by weight.
- the neutron-shielding hydraulic hardening material of the present invention provides a neutron-shielding product after being mixed with water and then setting. It is not necessarily preferred if the mixing ratio of powders to water is defined by the ratio of water content to cement content as in the case of ordinary mortar and cement. Instead, it is proper that the ratio be defined in terms of the entirety of powders and water. The ratio is preferably such that water is used in an amount of 15-50 parts by weight with respect to 100 parts by weight of the neutron-shielding hydraulic setting material of the present invention.
- the neutron-shielding hydraulic hardening material of the present invention when it is mixed with water, this may be achieved by the addition of water reducing agents or high-range water reducing agents. If lighter neutron-shielding products are desired, this may be achieved by adding air-entraining agents, foaming agents, or similar agents to thereby introduce very fine air bubbles in the material while maintaining the uniformity of the composition.
- the neutron-shielding hydraulic hardening material of the present invention may contain at least one chemical admixture selected from the group consisting of air-entraining agents, air-entraining and water reducing agents, high-range water reducing agents, plasticizers, air-entraining and high-range water reducing agents, and foaming agents.
- these are incorporated in a total amount of not more than 5 parts by weight per 100 parts by weight of the neutron-shielding hydraulic hardening material of the present invention. If the total amount of the additives is in excess of 5 parts by weight, the additives may become separated when mixed with water; thus these amounts are not preferred.
- a fresh mortar obtained through mixing neutron-shielding hydraulic hardening material of the present invention with water is uniform and has an appropriate softness and fluidity. Therefore, it can be uniformly placed into a formwork without the application of violent mechanical vibration as generated by a vibrator.
- This is advantageous because mortar can be placed uniformly and without leaving large voids into complex members to which rod type vibrators cannot be inserted. Consequently, placing work can be considerably simplified, dispersion in quality of afterhardening product that tends to occur due to the application of vibration is reduced, and separation of materials that tends to occur due to the application of vibration can also be avoided.
- neutron-shielding hydraulic hardening material of the present invention and the method of manufacturing neutron shields of the present invention will next be described in detail by way of example, which is given for the purpose of illustration only, and should thus not be construed as limiting the invention.
- the neutron-shielding hydraulic hardening materials shown in Table 1 were prepared.
- the hydraulic cement employed was an high-early-strength Portland cement having a specific surface area of not less than 4,000 cm 2 /g.
- Three types of aluminum hydroxide having different particle sizes were used including A (particle size centered between 1 and 5 ⁇ m), B (particle size centered between 10 and 20 ⁇ m), and C (particle size centered between 90 and 110 ⁇ m).
- the boron carbide employed was B 4 C (particle size centered between 100 and 150 ⁇ m). Given proportions of powders were mixed using a Henschel mixer for 10 minutes.
- each powder sample was mixed with water at a water/powder ratio of 27% by weight, and a flow value was determined in accordance with the flow test method provided in JIS R5201, to thereby assess the fluidity.
- the compressive strength is as small as 2.0 N/mm 2 , which cannot provide the resultant structure with sufficient strength.
- the cement content is 10% by weight or greater (Samples 2 through 11) a certain level of strength is secured and thus the material can be used in practice.
- the flow values are 220 or greater, with the mortar exhibiting even more improved fluidity with excellent results of visual observation of voids.
- Example 7 a typical sample that exhibited excellent fluidity was used. This sample was mixed with water and additives at the indicated water/powder proportions and in the amounts indicated in Table 2.
- the high-range water reducing agent employed was a product of Onoda Cement Corporation (SP-X), and the air-entraining agent was a product of Yamaso Chemical Co., Ltd. (Vinsol W).
- the air volume and the flow value without tapping (unit: mm) of the fresh mortar were determined.
- the flow value without tapping indicates the diameter of mortar spread in a circle on a plane when a cone filled with mortar was placed on the plane and the cone was then removed by being lifted upward.
- a mortar sample having the same composition was placed into a formwork having an inner diameter of 10 cm and a height of 20 cm without the application of vibration, and was then cured for 14 days.
- the size of voids in the cross section of the resultant afterhardening product was determined in the manner described in Example 1. The results are shown in Table 2.
- Sample 21 representing the standard in which no additives were added, exhibited a flow value without tapping of 105, which was almost the same as that of the bottom size of the flow cone, and an air volume of 2% by volume.
- Sample 22 in which a high-range water reducing agent had been added in an amount of 0.4% by weight
- Sample 23 in which an air-entraining agent had been added in an amount of 0.04% by weight
- Sample 24 in which a high-range water reducing agent and an air-entraining agent were simultaneously added
- Sample 24 exhibited slightly reduced effect of the additives, but still was considered satisfactory in terms of achievement of fluidity and a reduction in weight.
- Samples 22 and 24 (in which a high-range water reducing agent was added) show sufficient fluidity, and uniform afterhardening products having no large woids have been obtained by placing without being applied mechanical vibration.
- the neutron-shielding hydraulic setting material of the present invention is a material that provides an excellent neutron shielding effect, satisfactory strength of afterset product, and good workability of fresh mortar. Therefore, when neutron shields are manufactured by the method of the present invention, neutron shields with enhanced uniformity can be obtained.
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Abstract
Description
- The present invention relates to a neutron-shielding material which is useful in the fields of nuclear power plants, reprocessing of spent nuclear fuels, spent nuclear fuel disposal, medicine, etc., and particularly useful for shielding neutrons generated from various sources in such fields. The invention also relates to a method of manufacturing neutron shields.
- In recent years, the percentage of electric power generated by nuclear power plants has been increasing steadily. However, from the viewpoints of nuclear nonproliferation and, particularly in a country like Japan which has very limited natural resources, from the viewpoint of the need to secure effective natural resources, recycling of spent nuclear fuels has become one of the top priority issues. In the processes of nuclear power generation, a considerable amount of neutrons are generated by active nuclear reactions. Moreover, spent nuclear fuels and nuclear fuel wastes generate neutron rays during self-decay of the resultant fission products.
- In order to shield such highly energetic neutrons, it is required that the energetic neutrons be slowed down to thermal neutrons using elements having a small atomic mass number, e.g., hydrogen (H), and that the thermal neutrons be absorbed by a suitable substance such as boron (B). Thus, a material containing both hydrogen and boron at high concentrations is considered to be effective as a neutron shield.
- Cement is a relatively good material for shielding neutrons because, when transformed into mortar or concrete, it is mixed with water so as to form a hydrate that traps water therein. However, the amount of water bound as a constituent of hydrate is small, and the greater part of mixed water is free water, which is likely to be lost due to evaporation, etc. Plastics such as polyethylene may also contain a relatively large amount of hydrogen. However, generally speaking, plastics are weak against heat and have poor long-term durability. In addition, they are difficult to form into large members of high density. For these reasons, uses of plastics are limited.
- Exemplary substances containing boron include natural minerals such as colemanite (2CaO·3B2O3·5H2O) and kurnakovite (2MgO·3B2O3·13H2O). In order to shield neutrons, use of these minerals as aggregate of concrete may be conceivable. However, the boron content in these minerals is as low as 12-17% by weight, so it is difficult to secure boron content at a high concentration. Moreover, these minerals release B2O3, which inhibits cement from setting or hardening. To suppress release of B2O3, there has been made an attempt to coarsen the grain size of aggregate to thereby reduce specific surface area. This approach, however, cannot avoid uneven distribution of boron in concrete. In addition, control of grain size of powdery aggregate is difficult. As a result, it is not only impossible to obtain highly plasticized concrete, but it also becomes difficult to place concrete into a formwork uniformly.
- As described above, conventional neutron shields and materials therefor have the following drawbacks: Limited hydrogen content and boron content; low strength against heat and external physical force; a tendency to leave large voids in concrete products; difficulty in forming large members or members having complex shapes; and difficulty in obtaining shields having a uniform composition. Therefore, they are not satisfactory as neutron shields around nuclear reactors or high level radioactive waste.
- Under the above circumstances, the inventors of the present invention conducted careful studies, and found that hydraulic hardening materials containing hydraulic cement, aluminum hydroxide, and boron carbide at certain proportions have excellent neutron shielding properties, strength of afterhardening products, and workability of fresh mortar, and that they are capable of forming uniform shields. The present invention was accomplished based on these findings.
- Accordingly, the present invention provides a hydraulic hardening material for shielding neutrons (hereinafter may be referred to as neutron-shielding material) characterized by containing 10-50% by weight of hydraulic cement, 30-88% by weight of aluminum hydroxide, and 0.1-35% by weight of boron carbide.
- The present invention also provides a method of manufacturing a neutron shield including the steps of mixing 100 parts by weight of the above-mentioned neutron-shielding hydraulic hardening material, 15-50 parts by weight of water, and not more than 5 parts by weight of at least one chemical admixture selected from the group consisting of air-entraining (AE) agents, air-entraining and water reducing agents, high-range water reducing agents, plasticizers, air-entraining and high-range water reducing agents, and foaming agents; and kneading the resultant mixture.
- Among the constituents of the neutron-shielding hydraulic hardening material of the present invention, the hydraulic cement provides the target afterhardening structure with strength when mixed with water, aluminum hydroxide provides hydrogen atoms that slow down highly energetic neutrons to thermal neutrons, and boron carbide provides boron atoms that absorb thermal neutrons which have been slowed down by hydrogen atoms. These three constituents work together so as to exert a function as a neutron shield.
- Hydraulic cements are not particularly limited so far as they harden when mixed with water to thereby develop strength. For example, they may be any one of Portland cements such as ordinary Portland cement and high-early-strength Portland cement; blended cements such as Portland blast-furnace slag cement, Portland pozzolan cement, and Portland fly-ash cement; or ultra-rapid-hardening cement (Jet cement). In addition to these types of cement, there may be used admixtures such as blast-furnace slag, silica fume, fly ash, limestone powder, and gypsum. If needed, there may also be used additives that are ordinarily used in mortar and concrete; e.g., expansive additives, accelerator, corrosion inhibitor, and waterproofing agents.
- Aluminum hydroxide may take a polymorphism such as diaspore, boemite, and gibbsite. In consideration of stability at high temperatures, gibbsite is most preferred. The theoretical hydrogen content of gibbsite is 3.8% by weight.
- Boron carbides take the form of B4C, B8C, B13C2, etc. Under general circumstances, B4C is the easiest one to obtain. Moreover, B4C is preferred because of its good stability. The theoretical boron content of B4C is as high as 78% by weight.
- When a neutron-shielding hydraulic hardening material neutrons is mixed with water and thereby hardens to develop enough strength as a structure, it is necessary that hydraulic cement be present in the amount of at least 10% by weight.
If hydrogen and boron are both co-present, the neutron absorbing effect may be exerted more effectively.
Therefore, it is concluded that proper ranges for the content of hydraulic cement, aluminum hydroxide, and boron carbide are 10-50% by weight, 30-88% by weight, and 0.1-35% by weight, respectively. In this case, if 10B is extremely concentrated (in nature, 10B is present in an amount of about 20%), 0.1% by weight of boron carbide would yield an effect, whereas if boron present in nature is used, it must be incorporated in amounts of at least 0.5% by weight. - Hydraulic cement is obtained through grinding the clinker that has been burned in a rotary kiln, and mixing it with suitable admixtures such as gypsum. Aluminum hydroxide is usually manufactured using a Bayer's process for industrial production. Boron carbide is normally manufactured through carbonizing of boron oxide (B2O3) using carbon, and the resultant mass is used after being pulverized. Generally, hydraulic hardening materials obtained by the mixture of these heterogeneous powders have poor fluidity when mixed with water. In extreme cases, flow and slump are barely obtainable. In addition, ordinary tamping bars cannot achieve uniform filling of the cement into a flow cone or a slump cone; therefore a vibrator is usually required for achieving a uniform placing. Thus, in order to improve fluidity of mortar after the above-mentioned complexed powder has been mixed with water, the powder in a dry state preferably has a filling ratio of not lower than a threshold value.
Specifically, it is preferred that the filling rate be not less than 55%, more preferably not less than 60%, when measured in such a manner that the powder in a dry state is put in a hollow cylindrical container having an inner diameter of 5 cm and a height of 5 cm, and then compacted by 180 tappings from the height of 2 cm. - In order to enhance the filling ratio of the constituent powdery materials in a dry state to thereby improve the mortar fluidity, it is effective to broaden the distribution of the particle size of the powders.
Alternatively, groups of powders, having peaks at different positions of particle size distribution (i.e., at smaller particle sizes and at larger particle sizes) that are widely apart from one another, may be used. Specifically, it is preferred that the particles, when sieved through a mesh of 1 mm, be of such distribution that oversize particles are present in an amount of not more than 5% by weight, particles having a diameter of equal to or smaller than 100 µm are present in an amount of 60-80% by weight, and particles having a diameter of 60-90 µm are present in an amount of not more than 20% by weight. - The neutron-shielding hydraulic hardening material of the present invention provides a neutron-shielding product after being mixed with water and then setting. It is not necessarily preferred if the mixing ratio of powders to water is defined by the ratio of water content to cement content as in the case of ordinary mortar and cement.
Instead, it is proper that the ratio be defined in terms of the entirety of powders and water. The ratio is preferably such that water is used in an amount of 15-50 parts by weight with respect to 100 parts by weight of the neutron-shielding hydraulic setting material of the present invention. If the water content is less than 15 parts by weight, uniform mortar cannot be obtained, whereas if the water content is in excess of 50 parts by weight, not only is strength of the afterhardening product reduced significantly, but there is also caused considerable separation of materials at the time of concreat placement. - Also, if even more improved fluidity is desired for the neutron-shielding hydraulic hardening material of the present invention when it is mixed with water, this may be achieved by the addition of water reducing agents or high-range water reducing agents. If lighter neutron-shielding products are desired, this may be achieved by adding air-entraining agents, foaming agents, or similar agents to thereby introduce very fine air bubbles in the material while maintaining the uniformity of the composition. That is, the neutron-shielding hydraulic hardening material of the present invention may contain at least one chemical admixture selected from the group consisting of air-entraining agents, air-entraining and water reducing agents, high-range water reducing agents, plasticizers, air-entraining and high-range water reducing agents, and foaming agents. Preferably, these are incorporated in a total amount of not more than 5 parts by weight per 100 parts by weight of the neutron-shielding hydraulic hardening material of the present invention. If the total amount of the additives is in excess of 5 parts by weight, the additives may become separated when mixed with water; thus these amounts are not preferred.
- A fresh mortar obtained through mixing neutron-shielding hydraulic hardening material of the present invention with water is uniform and has an appropriate softness and fluidity. Therefore, it can be uniformly placed into a formwork without the application of violent mechanical vibration as generated by a vibrator. This is advantageous because mortar can be placed uniformly and without leaving large voids into complex members to which rod type vibrators cannot be inserted. Consequently, placing work can be considerably simplified, dispersion in quality of afterhardening product that tends to occur due to the application of vibration is reduced, and separation of materials that tends to occur due to the application of vibration can also be avoided.
- The neutron-shielding hydraulic hardening material of the present invention and the method of manufacturing neutron shields of the present invention will next be described in detail by way of example, which is given for the purpose of illustration only, and should thus not be construed as limiting the invention.
- The neutron-shielding hydraulic hardening materials shown in Table 1 were prepared. The hydraulic cement employed was an high-early-strength Portland cement having a specific surface area of not less than 4,000 cm2/g. Three types of aluminum hydroxide having different particle sizes were used including A (particle size centered between 1 and 5 µm), B (particle size centered between 10 and 20 µm), and C (particle size centered between 90 and 110 µm). The boron carbide employed was B4C (particle size centered between 100 and 150 µm). Given proportions of powders were mixed using a Henschel mixer for 10 minutes.
- Each of the obtained dry powder samples was evaluated in terms of the filling ratio [
- Next, each powder sample was mixed with water at a water/powder ratio of 27% by weight, and a flow value was determined in accordance with the flow test method provided in JIS R5201, to thereby assess the fluidity.
- Separately, mortar samples obtained through mixing under the same conditions as those described above were independently placed in a cylindrical formwork having an inner diameter of 10 cm and a height of 20 cm, and the samples were compacted for 5 seconds with vibration of a rod type vibrator. Subsequently, the compacted samples were cured for 14 days, after which time the compressive strength of each afterhardening product was measured. The cross section of the afterhardening product was also observed, and the size of voids were visually determined in accordance with the following criteria.
-
- A: Pores measuring 1 mm or greater are not present
- B: Pores measuring 1 mm or greater are present; but pores measuring 2 mm or greater are not present
- C: Pores measuring 2 mm or greater are present; but pores measuring 4 mm or greater are not present
- D: Pores measuring 4 mm or greater are present.
- From Table 1, the following are concluded:
- When the amount of cement if less than 10% (Sample 1), the compressive strength is as small as 2.0 N/mm2, which cannot provide the resultant structure with sufficient strength. However, when the cement content is 10% by weight or greater (Samples 2 through 11) a certain level of strength is secured and thus the material can be used in practice.
- When the filling ratio of dry powder is not less than 55% (Samples 3 through 11), flow values can be measured. However, when it is less than 55% (Samples 1 and 2), mortar placed in a flow cone develops cracks after being tapped 15 times. Thus, measurement of flow values cannot be performed. When the filling ratio is not less than 60% (Samples 3, 5, and 7 through 11), the flow values are 200 or greater, affording a good fluidity. Moreover, in the cases where the filling ratio is not less than 60%, particles having a diameter of not more than 100 µm are present in an amount of 60-80% by weight, and particles having a diameter of between 60 and 90 µm are present in an amount of not more than 20% by weight (Samples 3, 7, and 9 through 11), the flow values are 220 or greater, with the mortar exhibiting even more improved fluidity with excellent results of visual observation of voids.
- Among the samples of neutron-shielding hydraulic hardening material of the present invention tested in Example 1, a typical sample that exhibited excellent fluidity (Sample 7) was used. This sample was mixed with water and additives at the indicated water/powder proportions and in the amounts indicated in Table 2. The high-range water reducing agent employed was a product of Onoda Cement Corporation (SP-X), and the air-entraining agent was a product of Yamaso Chemical Co., Ltd. (Vinsol W).
- The air volume and the flow value without tapping (unit: mm) of the fresh mortar were determined. The flow value without tapping indicates the diameter of mortar spread in a circle on a plane when a cone filled with mortar was placed on the plane and the cone was then removed by being lifted upward. In addition, a mortar sample having the same composition was placed into a formwork having an inner diameter of 10 cm and a height of 20 cm without the application of vibration, and was then cured for 14 days. The size of voids in the cross section of the resultant afterhardening product was determined in the manner described in Example 1. The results are shown in Table 2.
- The following can be seen from Table 2.
- Sample 21, representing the standard in which no additives were added, exhibited a flow value without tapping of 105, which was almost the same as that of the bottom size of the flow cone, and an air volume of 2% by volume. In contrast, Sample 22 (in which a high-range water reducing agent had been added in an amount of 0.4% by weight) exhibited an increased flow value without tapping of 220 even though the water/powder ratio had been reduced to 23% by weight. Thus, fluidity was greatly improved. Sample 23 (in which an air-entraining agent had been added in an amount of 0.04% by weight) exhibited a high air content at 9% by volume. The air in this case was so finely dispersed that it could not be observed visually. Therefore, this did not result in an uneven composition. Sample 24 (in which a high-range water reducing agent and an air-entraining agent were simultaneously added) exhibited slightly reduced effect of the additives, but still was considered satisfactory in terms of achievement of fluidity and a reduction in weight.
- Samples 22 and 24 (in which a high-range water reducing agent was added) show sufficient fluidity, and uniform afterhardening products having no large woids have been obtained by placing without being applied mechanical vibration.
- As described above, the neutron-shielding hydraulic setting material of the present invention is a material that provides an excellent neutron shielding effect, satisfactory strength of afterset product, and good workability of fresh mortar. Therefore, when neutron shields are manufactured by the method of the present invention, neutron shields with enhanced uniformity can be obtained.
Claims (5)
- A neutron-shielding hydraulic hardening material characterized by containing 10-50% by weight of hydraulic cement, 30-88% by weight of aluminum hydroxide, and 0.1-35% by weight of boron carbide.
- A hydraulic hardening material for shielding neutrons as described claim 1, which has a filling rate of not less than 55% as measured in such a manner that the material in a dry state is put in a hollow cylindrical container having an inner diameter of 5 cm and a height of 5 cm, and then compacted by 180 tappings from the height of 2 cm.
- A neutron-shielding hydraulic hardening material as described in claim 1 or 2, which is constituted by particles comprising, when sieved through a mesh of 1 mm, not more than 5% by weight of oversize particles, 60-80% by weight of particles having a diameter of equal to or smaller than 100 µm, and not more than 20% by weight of particles having a diameter of 60-90 µm.
- A method of manufacturing a neutron shield characterized by comprising the steps of mixing 100 parts by weight of a neutron-shielding hydraulic hardening material as described in any one of claims 1 through 3, 15-50 parts by weight of water, and not more than 5 parts by weight of at least one chemical admixture selected from the group consisting of air-entraining agents, air-entraining and water reducing agents, high-range water reducing agents, plasticizers, air-entraining and high-range water reducing agents, and foaming agents; and kneading the resultant mixture.
- A method of manufacturing a neutron shield as described in claim 4, wherein the kneaded material is placed into a formwork without being applied mechanical vibration.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP294385/95 | 1995-11-13 | ||
JP7294385A JP2929077B2 (en) | 1995-11-13 | 1995-11-13 | Hydraulic material for neutron shielding and method of manufacturing neutron shielding body using the same |
JP29438595 | 1995-11-13 |
Publications (2)
Publication Number | Publication Date |
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EP0773555A1 true EP0773555A1 (en) | 1997-05-14 |
EP0773555B1 EP0773555B1 (en) | 2000-07-05 |
Family
ID=17807047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP96118207A Expired - Lifetime EP0773555B1 (en) | 1995-11-13 | 1996-11-13 | Neutron-shielding hydraulic hardening material and method of manufacturing neutron shields using the same |
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Country | Link |
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EP (1) | EP0773555B1 (en) |
JP (1) | JP2929077B2 (en) |
DE (1) | DE69609144T2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ304030B6 (en) * | 2011-11-14 | 2013-08-28 | Ústav anorganické chemie AV CR, v.v.i. | Inorganic material with neutron absorbers and process of its preparation |
JP2017062268A (en) * | 2017-01-16 | 2017-03-30 | 富士化学株式会社 | Criticality prevention coating layer and method for forming the same |
CN107342113A (en) * | 2017-07-21 | 2017-11-10 | 中国核动力研究设计院 | A kind of resistance to irradiation inorganic mask material of high temperature resistant |
CN111943612A (en) * | 2020-08-13 | 2020-11-17 | 中国核动力研究设计院 | Irradiation-resistant high-temperature-resistant fast neutron shielding material and preparation method thereof |
CN114171215A (en) * | 2021-12-01 | 2022-03-11 | 中国核电工程有限公司 | Neutron poison material, preparation method thereof and nuclear critical safety storage tank |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10327466B4 (en) * | 2003-01-13 | 2008-08-07 | Jan Forster | Structure for radiation protection structures |
JP2008157801A (en) * | 2006-12-25 | 2008-07-10 | Fujita Corp | Neutron shielding low-activation concrete and mortar |
JP4883634B2 (en) * | 2007-06-07 | 2012-02-22 | 株式会社フジタ | Neutron shield and accelerator chamber formed by the neutron shield |
JP5347075B1 (en) * | 2013-01-25 | 2013-11-20 | 石川島建材工業株式会社 | Neutron shielding concrete |
DE102017006902A1 (en) * | 2017-07-20 | 2019-01-24 | Theodor Pieper GmbH & Co. KG | Concrete composition and method of making such a concrete composition |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5416098A (en) * | 1976-05-12 | 1979-02-06 | Nippon Asbestos Co Ltd | Neutron shielding heat insulator |
FR2546331A1 (en) * | 1983-05-20 | 1984-11-23 | Robatel Slpi | Improvements to hydrogen-containing materials for antineutron protection |
JPH01147399A (en) * | 1987-12-02 | 1989-06-09 | Kuraray Co Ltd | Fiber-reinforced neutron shielding mortar concrete |
JPH0687639A (en) * | 1992-09-01 | 1994-03-29 | Kao Corp | Air-entraining agent |
JPH07165477A (en) * | 1993-12-13 | 1995-06-27 | Daido Concrete Kogyo Kk | Molded article of porous open-cell concrete and production of composite material of the same concrete |
-
1995
- 1995-11-13 JP JP7294385A patent/JP2929077B2/en not_active Expired - Fee Related
-
1996
- 1996-11-13 EP EP96118207A patent/EP0773555B1/en not_active Expired - Lifetime
- 1996-11-13 DE DE69609144T patent/DE69609144T2/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5416098A (en) * | 1976-05-12 | 1979-02-06 | Nippon Asbestos Co Ltd | Neutron shielding heat insulator |
FR2546331A1 (en) * | 1983-05-20 | 1984-11-23 | Robatel Slpi | Improvements to hydrogen-containing materials for antineutron protection |
JPH01147399A (en) * | 1987-12-02 | 1989-06-09 | Kuraray Co Ltd | Fiber-reinforced neutron shielding mortar concrete |
JPH0687639A (en) * | 1992-09-01 | 1994-03-29 | Kao Corp | Air-entraining agent |
JPH07165477A (en) * | 1993-12-13 | 1995-06-27 | Daido Concrete Kogyo Kk | Molded article of porous open-cell concrete and production of composite material of the same concrete |
Non-Patent Citations (4)
Title |
---|
DATABASE WPI Section Ch Week 7911, Derwent World Patents Index; Class K07, AN 79-20806B, XP002023883 * |
DATABASE WPI Section Ch Week 8929, Derwent World Patents Index; Class A93, AN 89-210259, XP002023882 * |
PATENT ABSTRACTS OF JAPAN vol. 018, no. 347 (C - 1219) 30 June 1994 (1994-06-30) * |
PATENT ABSTRACTS OF JAPAN vol. 95, no. 006 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ304030B6 (en) * | 2011-11-14 | 2013-08-28 | Ústav anorganické chemie AV CR, v.v.i. | Inorganic material with neutron absorbers and process of its preparation |
JP2017062268A (en) * | 2017-01-16 | 2017-03-30 | 富士化学株式会社 | Criticality prevention coating layer and method for forming the same |
CN107342113A (en) * | 2017-07-21 | 2017-11-10 | 中国核动力研究设计院 | A kind of resistance to irradiation inorganic mask material of high temperature resistant |
CN111943612A (en) * | 2020-08-13 | 2020-11-17 | 中国核动力研究设计院 | Irradiation-resistant high-temperature-resistant fast neutron shielding material and preparation method thereof |
CN114171215A (en) * | 2021-12-01 | 2022-03-11 | 中国核电工程有限公司 | Neutron poison material, preparation method thereof and nuclear critical safety storage tank |
Also Published As
Publication number | Publication date |
---|---|
JP2929077B2 (en) | 1999-08-03 |
JPH09133790A (en) | 1997-05-20 |
EP0773555B1 (en) | 2000-07-05 |
DE69609144T2 (en) | 2001-03-22 |
DE69609144D1 (en) | 2000-08-10 |
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