WO2014148466A1 - 塗布型放射線遮蔽材及び放射線遮蔽性エラストマー材料 - Google Patents
塗布型放射線遮蔽材及び放射線遮蔽性エラストマー材料 Download PDFInfo
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- WO2014148466A1 WO2014148466A1 PCT/JP2014/057268 JP2014057268W WO2014148466A1 WO 2014148466 A1 WO2014148466 A1 WO 2014148466A1 JP 2014057268 W JP2014057268 W JP 2014057268W WO 2014148466 A1 WO2014148466 A1 WO 2014148466A1
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- 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
- G21F1/10—Organic substances; Dispersions in organic carriers
- G21F1/103—Dispersions in organic carriers
- G21F1/106—Dispersions in organic carriers metallic dispersions
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D119/00—Coating compositions based on rubbers, not provided for in groups C09D107/00 - C09D117/00
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- 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
- G21F3/00—Shielding characterised by its physical form, e.g. granules, or shape of the material
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
- C08K2003/0887—Tungsten
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
Definitions
- the present invention relates to a coating-type radiation shielding material and a radiation shielding elastomer material cured using this material.
- Radiation includes alpha rays, beta rays, and neutron rays, which are particle rays, and gamma rays and X rays, which are electromagnetic waves.
- Alpha rays are weakly permeable and can be shielded even with a sheet of paper, and beta rays are also a few mm thick aluminum. Can be prevented with foil.
- gamma rays have strong penetrating power, and a thickness of 29 cm is required for concrete and 2.5 cm for lead to obtain a 90% shielding rate.
- Neutron beams are more penetrating and can only be blocked by hydrogen atoms contained in thick walls of water or concrete.
- iron although density lighter than the 7.8 g / cm 3 and 11.3 g / cm 3 of lead, in order to obtain a 90% Cs137 gamma ray shielding rate required 75mm compared to NamariAtsu of 25mm As a result, the weight is about twice that of lead and cannot be an effective shielding material.
- Patent Document 7 there is a technique that uses a solvent to reduce the liquid viscosity of the shielding material and enables casting into a mold.
- the thickness of the sheet and the molded body is described as 5 mm at the maximum, and it is said that it is possible to use the thickness more than that, but it is difficult to maintain the shape due to the increase in the number of sheets. It is difficult to apply widely.
- the radiation shielding rate is greatly influenced by the density of the shielding material, in Patent Documents 3 and 4, the filling rate of heavy metals and the like is low, and therefore the density of the shielding material is small, so that the X-ray shielding rate is also small.
- the heavy metal filling rate is set to 90% by weight or more, and the density of the shielding material is increased to the level of lead to ensure a shielding rate equivalent to lead. is there.
- the object is to obtain a radiation shielding material capable of forming an elastic coating film exceeding 10 cm by coating or casting while the density is equivalent to iron and the radiation shielding ratio is almost equivalent to lead. .
- the shielding material also enables thick film sheet processing.
- a high-concentration tungsten powder having a high radiation shielding power is blended in an elastomer precursor having a liquid viscosity of 10 to 1000 mPa ⁇ s, and the mixture is kept at 50 to 80 ° C. and stirred at a high speed with a disper, Obtain a low-viscosity liquid from 4,000 to 20,000 mPa ⁇ s and form it freely by coating or casting to obtain an elastic coating film from a thin film of about 50 ⁇ m to a thick film exceeding 10 cm. It has been solved.
- a sheet processing of 0.5 to 1 mm is performed using a shielding material liquid obtained by evaporating a solvent contained in a small amount in the radiation shielding material to obtain a highly viscous liquid of 50,000 to 100,000 mPa ⁇ s.
- the problem is solved by obtaining a sheet up to about 10 mm thick by laminating and thermocompression bonding.
- a coating-type radiation shielding material comprising tungsten powder, an elastomer precursor, and a lithium compound.
- Radiation shielding material has a solid content of 50 to 100 wt%, and a viscosity of 10 to 1000 mPa ⁇ s.
- Radiation shielding material [3] The radiation shielding material according to [1], wherein the blending ratio of the tungsten powder and the elastomer precursor is 5:95 to 20:80 (parts by weight) as a solid content.
- [6] The coating type radiation shielding material according to any one of [1] to [5] above, comprising (1) boron or boron compound powder, or (2) ferrite powder.
- [7] The coating type radiation shielding material according to any one of [1] to [5] above, comprising (1) boron or a boron compound powder, and (2) a ferrite powder.
- [8] A radiation shielding elastomer material obtained by applying and curing the coating type radiation shielding material according to any one of [1] to [7] on a substrate surface.
- the radiation shielding material obtained in the present invention can be cured by a crosslinking reaction or the like by room temperature and heating, and a cured radiation shielding material having elasticity can be produced. Because it has elasticity, it is resistant to impact and does not crack even when it is thickened. Moreover, sewing processing etc. are also attained by thin film formation.
- the present invention it is possible to produce a coating material, a casting mold, and a sheet processing capable of producing a cured shielding material having a high radiation shielding rate equivalent to that of lead at an iron-like density in a free form and thickness.
- a radiation shielding material can be provided. This makes it possible to reduce the weight of radiation waste containers and storage containers, radiation shields of existing and new structures and buildings, and radiation shield protective clothing while ensuring a high radiation shielding rate.
- This invention increases the radiation shielding rate by increasing the density of the shielding material by blending tungsten powder or the like in a high concentration with the elastomer precursor having a liquid property, and leaves the coating / casting / sheet processing characteristics,
- a coating-type radiation shielding material and its cured product which are characterized by being cured by a crosslinking reaction or the like after the operation of coating, etc., and further improving the radiation shielding rate by adding a lithium compound or the like. is there.
- the solid content (residue after heating at 105 ° C. for 3 hours) of the elastomer precursor cured by a crosslinking reaction after coating is preferably 30 to 100 wt%, and more preferably 50 to 100 wt%.
- the solid content is lower than 30 wt%, the volatile components present in the shielding material increase, and after evaporation, a large amount of voids are formed in the cured product, resulting in a decrease in the shielding rate.
- the viscosity of the elastomer precursor is preferably 1 to 2000 mPa ⁇ s, more preferably 10 to 1000 mPa ⁇ s. If the viscosity is lower than 1 mPa ⁇ s, the viscosity of the shielding material becomes too low, and the tungsten powder may settle and separate. On the other hand, if the viscosity is higher than 2000 mPa ⁇ s, it becomes difficult to blend the tungsten powder at a high concentration, and the viscosity of the shielding material becomes too high to be applied.
- the mixing ratio of the elastomer precursor and tungsten powder according to the present invention is preferably 3:97 to 25:75 by weight, and more preferably 5:95 to 20:80. If the mixing ratio is less than 3:97, it becomes difficult to form a sound coating film by coating, and the adhesion and strength after curing will be insufficient. On the other hand, when the mixing ratio is larger than 25:75, the density of the shielding material is lowered, and a high radiation shielding rate cannot be ensured.
- the elastomer precursor examples include thermosetting elastomers, natural rubber and synthetic rubber before crosslinking reaction, such as acrylic rubber, nitrile rubber, isoprene rubber, urethane rubber, ethylene propylene rubber, chlorosulfonated polyethylene rubber, epichlorohydrin rubber, chloroprene.
- thermosetting elastomers such as acrylic rubber, nitrile rubber, isoprene rubber, urethane rubber, ethylene propylene rubber, chlorosulfonated polyethylene rubber, epichlorohydrin rubber, chloroprene.
- examples thereof include rubber, silicone rubber, styrene / butadiene rubber, fluorine rubber, and polyisobutylene rubber.
- thermoplastic elastomers such as styrene, olefin, vinyl chloride, urethane, ester, amide and the like can be mentioned.
- the tungsten powder preferably has an average particle size of 0.5 to 10 ⁇ m, more preferably 1 to 5 ⁇ m. If the average particle size is smaller than 0.5 ⁇ m, it is necessary to add many elastomer precursors in order to obtain a coating-type shielding material, making it difficult to blend a high concentration of tungsten, while the average particle size is larger than 10 ⁇ m. Then, the tungsten powder tends to settle, making it difficult to use as a coating type shielding material.
- lithium compound examples include lithium chloride, lithium fluoride, lithium bromide, lithium iodide, lithium hydroxide, lithium hexafluorotrilophosphate, lithium niobate, n-butyl lithium, lithium acetate, lithium carbonate, lithium citrate. And lithium orophosphate.
- the addition amount of these lithium compounds is preferably 0.1 to 3.0 parts by weight, more preferably 0.2 to 1.0 parts by weight, based on 100 parts by weight of the total amount of the elastomer precursor and the tungsten powder. When the addition amount is less than 0.1 parts by weight, the radiation shielding rate is not improved.
- the addition amount exceeds 3.0 parts by weight, the amount of the solvent for dissolving the lithium compound increases, so that the liquid viscosity of the radiation shielding material is increased. There is a possibility that the tungsten powder may be settled and separated, and pinholes may be generated in the coating film due to the evaporation of a large amount of solvent, resulting in non-uniform radiation shielding.
- a strontium compound, a magnesium compound, and a lanthanoid element compound such as a europium compound, an erbium compound, and a dysprosium compound may be added singly or in combination.
- strontium carbonate, magnesium oxide, europium oxide, erbium oxide, and dysprosium oxide can be added singly or in combination.
- These addition amounts are preferably 0.5 to 5.0 parts by weight, more preferably 1.0 to 3.0 parts by weight, based on 100 parts by weight of the total amount of the elastomer precursor and the tungsten powder. When the addition amount is less than 0.5 parts by weight, the radiation shielding rate is not improved, and when it exceeds 5.0 parts by weight, the effect of improving the shielding rate by increasing the addition amount is reduced.
- boron or boron compound powder, molybdenum powder, silver powder and other compounds having radiation shielding ability may be added.
- the shape is not limited to a spherical shape, and may be a flake shape, a needle shape, a fiber shape, or the like.
- the radiation shielding material of the coating or casting mold according to this invention it is possible to produce a radiation shielding material cured product of various shapes and thicknesses, a radiation shielding room for securing a work space in a radiation environment, radioactive It can be used for storage containers and transport containers for waste containing substances, protective clothing and equipment for preventing radiation exposure in a radiation environment including medical sites.
- lithium citrate Strontium carbonate, europium oxide, erbium oxide, dysprosium oxide: strontium carbonate, europium oxide, erbium oxide, dysprosium oxide produced by Wuxi Decorative Prodcts Co., Ltd Called dysprosium
- the prepared radiation shielding material is poured into an acrylic box with a side wall of a certain height and a thickness of 5 mm and left at room temperature for 24 hours to produce cured radiation shielding materials having various thicknesses.
- the shielding rate of gamma rays was measured using a radiation source number 8101 ⁇ 10 MBq.
- Example 2 Results of carrying out an evaluation test in the same manner as in Example 1 using a shielded cured product (density 7.8 g / cm 3 ) obtained in the same manner as in Example 1 except that lithium citrate was used as the lithium compound. Is shown in Table 2.
- Table 3 shows the results of an evaluation test conducted in the same manner as in Example 1 using the shielding material cured product (density 7.8 g / cm 3 ) obtained in the same manner as in Example 1 except that no lithium compound was added. Show.
- Example 4 A 5 mm thick shield obtained in the same manner as in Example 1 except that 2.0 parts by weight of a methanol solution of lithium acetate in Example 1 was added, and then strontium carbonate, europium oxide, erbium oxide, and dysprosium oxide were added.
- Table 4 shows the results of an evaluation test using the cured material in the same manner as in Example 1 and the results of measuring the gamma ray shielding rate using Cobalt 60 radiation source number 2225.
- Table 5 shows the results of casting the radiation shielding material prepared in the same manner as in Example 1 into a steel box having a bottom plate thickness of 12 mm having a side wall of a certain height and carrying out an evaluation test in the same manner as in Example 1. Show.
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Abstract
Description
また、コンクリートは、特許文献1、2、及び非特許文献1にあるように、高い遮蔽率を得るためには厚みを増す必要があり、固定建造物であれば問題ないが、放射性物質の保管・搬送に用いるドラム缶やコンテナの容器サイズになると収容できる量も少なくなり、さらに容器重量が重くなり搬送に問題を生じるとともに、コンクリートは水和反応の進捗とともにひび割れを起こすことも多く、内容物の漏れ出しの危険性もある。
一方、鉄は、密度が7.8g/cm3と鉛の11.3g/cm3と比べて軽いものの、Cs137ガンマ線遮蔽率90%を得るためには、鉛厚さ25mmに比べ75mmが必要となることで、重量が鉛の2倍程度となり、有効な遮蔽材とはなりえない
また、特許文献7のように、溶剤を用いることで遮蔽材の液粘度を低下させ、型への流し込み成形を可能としたものもある。
但し、シートおよび成形体の厚さは最大でも5mmと記載されており、それ以上の厚さについては重ねて使用することができるとされているが、シート枚数の増加により、形状の保持が困難になるといったこともあることから幅広い適用は難しい。
更に、放射線の遮蔽率は遮蔽材の密度に大きく影響されるため、特許文献3、4においては、重金属等の充填率が低く、よって遮蔽材の密度が小さいことにより、そのエックス線遮蔽率も小さいものとなっているが、特許文献5、6、7においては重金属の充填率を90重量%以上とし、遮蔽材の密度を鉛程度まで上げて、鉛並みの遮蔽率を確保できているものもある。
また、上記放射線遮蔽材中に少量含有される溶剤を蒸発させて、50,000から100,000mPa・sの高粘稠液とした遮蔽材液を用いて、0.5から1mmのシート加工を行い、それを積層し熱圧着することにより厚さ10mm程度までのシートを得ることにより問題を解決したものである。
[1] タングステン粉末、エラストマー前駆体及びリチウム化合物とからなることを特徴とする塗布型放射線遮蔽材。
[2] 前記エラストマー前駆体は、更に架橋等の硬化反応を行うことができ、固形分が50~100wt%、粘度が10~1000mPa・sであることを特徴とする前項[1]に記載の放射線遮蔽材。
[3] タングステン粉末とエラストマー前駆体の配合比が固形分として5:95~20:80(重量部比)であることを特徴とする前項[1]に記載の放射線遮蔽材。
[5] ストロンチウム化合物、マグネシウム化合物、及びランタノイド元素化合物例えばユウロピウム化合物、エルビウム化合物およびジスプロシウム化合物を単独もしくは複数種混合して含有することを特徴とする前項[1]~[4]のいずれか1項に記載の放射線遮蔽材。
[7] (1)ホウ素又はホウ素化合物粉末、及び(2)フェライト粉末を含有することを特徴とする前項[1]~[5]のいずれか1項に記載の塗布型放射線遮蔽材。
[8] 前項[1]~[7]のいずれか1項に記載の塗布型放射線遮蔽材を基材面に塗布し硬化させてなることを特徴とする放射線遮蔽性エラストマー材料。
この発明は、液性状を持つエラストマー前駆体にタングステン粉末等を高濃度配合させることで遮蔽材を高密度化させて放射線遮蔽率を大きくし、かつ塗布・流し込み成形・シート加工特性を残存させ、塗布等の操作後に架橋反応等により硬化させて塗膜化させることを特長としており、またリチウム化合物等を添加することによって更に放射能遮蔽率を向上させた塗布型放射線遮蔽材とその硬化物である。
これらリチウム化合物の添加量は、エラストマー前駆体とタングステン粉末の合計100重量部に対して0.1~3.0重量部が好ましく、0.2~1.0重量部がより好ましい。添加量が0.1重量部未満では、放射線遮蔽率の向上が見られず、3.0重量部を超えると、リチウム化合物を溶解させる溶剤量が多くなることで、放射線遮蔽材の液粘度が低下しタングステン粉末が沈降分離する恐れがあるとともに、溶剤の多量蒸発による塗膜にピンホールが発生し放射線遮蔽が不均一となる恐れがある。
これらの添加量は、エラストマー前駆体とタングステン粉末の合計100重量部に対して0.5~5.0重量部が好ましく、1.0~3.0重量部がより好ましい。添加量が0.5重量部未満では放射線遮蔽率の向上が見られず、5.0重量部を超えると、添加量増加による遮蔽率向上効果が小さくなる。
矩形をなす平鋼および/または溝形鋼にこの放射線高遮蔽材を塗布してなる遮蔽パネルを作製し、これらを組み立てることにより放射線の高遮蔽率を確保できる組み立てコンテナおよび遮蔽塀を提供することもでき、また容器を2重化し、その内側と外側容器の間の空隙にこの遮蔽材を流し込み成形することにより、任意の遮蔽率をもった遮蔽容器および遮蔽パネルを制作することが可能となる。さらに遮蔽材をシート化し、これを任意な形状に切断し鋼等の基材に貼り付けることにより遮蔽壁等の制作することが可能となる。
エラストマー前駆体
一液RTVゴム:信越化学工業(株)製KE-4895-T(以下「KE4895」と称する)室温硬化型シリコーンゴム。粘度500mPa・s
タングステン粉末
(株)アライドマテリアル製タングステン粉C20(以下「C20」と称する)
リチウム化合物
酢酸リチウム:和光純薬工業(株)製酢酸リチウム(以下「酢酸リチウム」と称する)
クエン酸リチウム:和光純薬工業(株)製クエン酸リチウム(以下「クエン酸リチウム」と称する)
炭酸ストロンチウム、酸化ユウロピウム、酸化エルビウム、酸化ジスプロシウム:Wuxi Decorative Prodcts Co.,Ltd製炭酸ストロンチウム、酸化ユウロピウム、酸化エルビウム、酸化ジスプロシウム(以下「炭酸ストロンチウム」、「酸化ユウロピウム」、「酸化エルビウム」、「酸化ジスプロシウム」と称する)
一定高さの側壁を持った底板厚さ5mmのアクリル箱に、調製した放射線遮蔽材を流し込み、常温で24時間放置することにより、種々厚みを持った放射線遮蔽材硬化物を作製し、セシウム137線源番号8101・10MBqを用いてガンマ線の遮蔽率を測定した。
プライミクス(株)T.K.ホモディスパーModel2.5(俗称ラボディスパー)により、8.0重量部のKE4895に対して、酢酸リチウム0.4重量部をメタノール1.6重量部により溶解した酢酸リチウム溶液2.0重量部およびトルエン4.0重量部を加え、1,000RPMにて15分程度撹拌し、次いで、ラボディスパー容器を70℃に設定されたウォーターバス中に設置し、撹拌速度を3,000RPMに上げて、92.0重量部のC20を徐々に添加し、液温度を70℃に維持しつつ約30分間攪拌した後、常温付近まで冷却し、これに純水0.2重量部を添加して5分間撹拌混合し、放射線遮蔽材を調製した。この遮蔽材の粘度は、6,000mPa・sであった。またこの遮蔽材から作製された遮蔽材硬化物の密度は7.8g/cm3であった。この遮蔽材硬化物のガンマ線遮蔽率の評価試験結果を表1に示す。
実施例1において酢酸リチウムのメタノール溶液2.0重量部を添加した後、炭酸ストロンチウム、酸化ユウロピウム、酸化エルビウムおよび酸化ジスプロシウムを加えた以外は実施例1と同様にして得られた5mm厚さの遮蔽材硬化物を用いて、実施例1と同様に評価試験を実施した結果およびコバルト60線源番号2225を用いてガンマ線遮蔽率を測定した結果を表4に示す。
Claims (8)
- タングステン粉末、エラストマー前駆体及びリチウム化合物とからなることを特徴とする塗布型放射線遮蔽材。
- 前記エラストマー前駆体は、更に架橋等の硬化反応を行うことができ、固形分が50~100wt%、粘度が10~1000mPa・sであることを特徴とする請求項1に記載の放射線遮蔽材。
- タングステン粉末とエラストマー前駆体の配合比が固形分として5:95~20:80であることを特徴とする請求項1に記載の放射線遮蔽材。
- 前記リチウム化合物の前記エラストマー前駆体と前記タングステン粉末の混合物100重量部に対する配合比が0.1~2.0重量部であることを特徴とする請求項1に記載の放射線遮蔽材。
- ストロンチウム化合物、マグネシウム化合物、及びランタノイド元素化合物例えばユウロピウム化合物、エルビウム化合物およびジスプロシウム化合物を単独もしくは複数種混合して含有することを特徴とする請求項1~4のいずれか1項に記載の放射線遮蔽材。
- (1)ホウ素又はホウ素化合物粉末、又は(2)フェライト粉末を含有することを特徴とする請求項1~5のいずれか1項に記載の塗布型放射線遮蔽材。
- (1)ホウ素又はホウ素化合物粉末、及び(2)フェライト粉末を含有することを特徴とする請求項1~5のいずれか1項に記載の塗布型放射線遮蔽材。
- 請求項1~7のいずれか1項に記載の塗布型放射線遮蔽材を基材面に塗布し硬化させてなることを特徴とする放射線遮蔽性エラストマー材料。
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WO2016068241A1 (ja) * | 2014-10-30 | 2016-05-06 | 株式会社Ricanal | シート状放射線遮蔽材 |
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---|---|---|---|---|
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Citations (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57172297A (en) * | 1981-04-17 | 1982-10-23 | Showa Denko Kk | Neutron shielding material |
JPH08201581A (ja) * | 1995-01-30 | 1996-08-09 | Sutaaraito Kogyo Kk | 放射線遮蔽用組成物並びにその用途 |
JPH10153690A (ja) | 1997-11-28 | 1998-06-09 | Hitachi Ltd | 放射性廃棄物充填容器及び放射性廃棄物の固化体 |
JP2001511202A (ja) * | 1997-01-30 | 2001-08-07 | スペース エレクトロニクス,インコーポレイテッド | 放射線遮蔽材をイオン化するための方法及び組成物関連出願のクロスレファレンス |
JP2001242288A (ja) * | 2000-02-29 | 2001-09-07 | Toshiba Corp | 放射線遮蔽素材、同素材を用いた放射線遮蔽服、放射線遮蔽盾および放射線遮蔽機器 |
WO2001099119A1 (fr) * | 2000-06-20 | 2001-12-27 | Kanebo, Limited | Materiau de protection contre les rayonnements |
JP2002048892A (ja) * | 2000-08-04 | 2002-02-15 | Daicel Chem Ind Ltd | 放射線遮蔽用樹脂組成物およびその製法 |
JP2003004892A (ja) * | 2001-04-16 | 2003-01-08 | Kanebo Ltd | 放射線遮蔽容器 |
JP2003287590A (ja) | 2003-05-09 | 2003-10-10 | Sumitomo Electric Ind Ltd | 放射線遮蔽材 |
JP2004523759A (ja) * | 2001-03-12 | 2004-08-05 | ノースロップ・グルマン・ニューポート・ニューズ | 放射線シールディング |
JP2004531730A (ja) * | 2001-05-21 | 2004-10-14 | ルメール パクス | 新しい放射線減衰材料及びその製造方法 |
JP2006258459A (ja) | 2005-03-15 | 2006-09-28 | Magx Co Ltd | 可撓性放射線遮蔽・遮音材 |
JP2008175811A (ja) | 2006-12-19 | 2008-07-31 | Nippon Tungsten Co Ltd | 電子線遮蔽用シート |
JP2008538136A (ja) * | 2004-12-20 | 2008-10-09 | メリディアン リサーチ アンド ディベロップメント | 放射線検出性防護物品 |
JP2009276194A (ja) | 2008-05-14 | 2009-11-26 | Toden Kogyo Co Ltd | 放射線遮蔽用コンクリート組成物及びその打設装置並びに放射性廃棄物収容器 |
JP2011099791A (ja) | 2009-11-06 | 2011-05-19 | Kitagawa Ind Co Ltd | 放射線遮蔽シート |
JP2012230101A (ja) * | 2011-04-13 | 2012-11-22 | Sanyo Chem Ind Ltd | 放射線遮蔽用組成物 |
JP2013018878A (ja) | 2011-07-12 | 2013-01-31 | Trust Life:Kk | 不燃及び放射線遮蔽シート |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3609372A (en) * | 1963-06-04 | 1971-09-28 | Marxen Friedrich | Shaped polymeric shield against neutron and gamma radiation |
US6261508B1 (en) | 1994-04-01 | 2001-07-17 | Maxwell Electronic Components Group, Inc. | Method for making a shielding composition |
US20030102463A1 (en) | 2001-03-12 | 2003-06-05 | Smith David M. | Radiation shielding |
US6608319B2 (en) * | 2001-06-08 | 2003-08-19 | Adrian Joseph | Flexible amorphous composition for high level radiation and environmental protection |
US20040124374A1 (en) * | 2001-06-08 | 2004-07-01 | Adrian Joseph | Amorphous composition for high level radiation and environmental protection |
JP2003255081A (ja) * | 2002-03-04 | 2003-09-10 | National Maritime Research Institute | 放射線遮蔽材組成物 |
FR2847352B1 (fr) | 2002-11-18 | 2005-01-28 | Airbus France | Systeme de commandes de vol electriques pour aeronef comportant une detection de couplages oscillatoires de pilotage et organe de pilotage pour un tel systeme |
DE50304311D1 (de) * | 2002-12-17 | 2006-08-31 | Lanxess Deutschland Gmbh | Bleifreie mischung als strahlenschutz-additiv |
US20070102672A1 (en) * | 2004-12-06 | 2007-05-10 | Hamilton Judd D | Ceramic radiation shielding material and method of preparation |
US20080085962A1 (en) * | 2006-10-06 | 2008-04-10 | General Electric Company | Composition and associated method |
KR100860333B1 (ko) * | 2008-08-26 | 2008-09-25 | 주식회사 텍시빌 | 방사선 차폐재 |
KR20100047510A (ko) * | 2008-10-29 | 2010-05-10 | 한국원자력연구원 | 나노 크기의 방사선 차폐물질을 포함하는 방사선 차폐재 및이의 제조방법 |
JP4779029B2 (ja) * | 2009-03-26 | 2011-09-21 | 義正 穴山 | 可撓性中性子遮蔽材、可撓性中性子遮蔽材製造用ストック、中性子遮蔽用テープ、中性子遮蔽用パッキング、および中性子遮蔽用充填材 |
JP5145507B1 (ja) * | 2011-09-14 | 2013-02-20 | 株式会社カワハラ技研 | 放射線遮蔽材及びその製造方法 |
-
2014
- 2014-03-17 JP JP2014053979A patent/JP6433134B2/ja active Active
- 2014-03-18 WO PCT/JP2014/057268 patent/WO2014148466A1/ja active Application Filing
- 2014-03-18 EP EP14769239.6A patent/EP2977990B1/en active Active
- 2014-03-18 CN CN201480016898.XA patent/CN105144303B/zh active Active
- 2014-03-18 US US14/778,393 patent/US9947424B2/en active Active
Patent Citations (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57172297A (en) * | 1981-04-17 | 1982-10-23 | Showa Denko Kk | Neutron shielding material |
JPH08201581A (ja) * | 1995-01-30 | 1996-08-09 | Sutaaraito Kogyo Kk | 放射線遮蔽用組成物並びにその用途 |
JP2001511202A (ja) * | 1997-01-30 | 2001-08-07 | スペース エレクトロニクス,インコーポレイテッド | 放射線遮蔽材をイオン化するための方法及び組成物関連出願のクロスレファレンス |
JPH10153690A (ja) | 1997-11-28 | 1998-06-09 | Hitachi Ltd | 放射性廃棄物充填容器及び放射性廃棄物の固化体 |
JP2001242288A (ja) * | 2000-02-29 | 2001-09-07 | Toshiba Corp | 放射線遮蔽素材、同素材を用いた放射線遮蔽服、放射線遮蔽盾および放射線遮蔽機器 |
WO2001099119A1 (fr) * | 2000-06-20 | 2001-12-27 | Kanebo, Limited | Materiau de protection contre les rayonnements |
JP2002048892A (ja) * | 2000-08-04 | 2002-02-15 | Daicel Chem Ind Ltd | 放射線遮蔽用樹脂組成物およびその製法 |
JP2004523759A (ja) * | 2001-03-12 | 2004-08-05 | ノースロップ・グルマン・ニューポート・ニューズ | 放射線シールディング |
JP2003004892A (ja) * | 2001-04-16 | 2003-01-08 | Kanebo Ltd | 放射線遮蔽容器 |
JP2004531730A (ja) * | 2001-05-21 | 2004-10-14 | ルメール パクス | 新しい放射線減衰材料及びその製造方法 |
JP2003287590A (ja) | 2003-05-09 | 2003-10-10 | Sumitomo Electric Ind Ltd | 放射線遮蔽材 |
JP2008538136A (ja) * | 2004-12-20 | 2008-10-09 | メリディアン リサーチ アンド ディベロップメント | 放射線検出性防護物品 |
JP2006258459A (ja) | 2005-03-15 | 2006-09-28 | Magx Co Ltd | 可撓性放射線遮蔽・遮音材 |
JP2008175811A (ja) | 2006-12-19 | 2008-07-31 | Nippon Tungsten Co Ltd | 電子線遮蔽用シート |
JP2009276194A (ja) | 2008-05-14 | 2009-11-26 | Toden Kogyo Co Ltd | 放射線遮蔽用コンクリート組成物及びその打設装置並びに放射性廃棄物収容器 |
JP2011099791A (ja) | 2009-11-06 | 2011-05-19 | Kitagawa Ind Co Ltd | 放射線遮蔽シート |
JP2012230101A (ja) * | 2011-04-13 | 2012-11-22 | Sanyo Chem Ind Ltd | 放射線遮蔽用組成物 |
JP2013018878A (ja) | 2011-07-12 | 2013-01-31 | Trust Life:Kk | 不燃及び放射線遮蔽シート |
Non-Patent Citations (2)
Title |
---|
DEVELOPMENT OF RADIOACTIVE WASTE STORAGE CONTAINER WHILE TAKING INTO ACCOUNT MOVEMENT CAPABLE OF ENHANCING SHIELDING FUNCTION AND SHIELDING CAPABILITY EXPERIMENTS |
See also references of EP2977990A4 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016068241A1 (ja) * | 2014-10-30 | 2016-05-06 | 株式会社Ricanal | シート状放射線遮蔽材 |
CN110289115A (zh) * | 2019-02-22 | 2019-09-27 | 西南科技大学 | 一种高强型硅橡胶基柔性中子屏蔽材料及其制备方法 |
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CN105144303B (zh) | 2018-05-08 |
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