JPS6329728Y2 - - Google Patents
Info
- Publication number
- JPS6329728Y2 JPS6329728Y2 JP1979113980U JP11398079U JPS6329728Y2 JP S6329728 Y2 JPS6329728 Y2 JP S6329728Y2 JP 1979113980 U JP1979113980 U JP 1979113980U JP 11398079 U JP11398079 U JP 11398079U JP S6329728 Y2 JPS6329728 Y2 JP S6329728Y2
- Authority
- JP
- Japan
- Prior art keywords
- component
- heat
- containers
- container
- temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000292 calcium oxide Substances 0.000 claims description 10
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- 239000000155 melt Substances 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 3
- 239000008187 granular material Substances 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 238000002425 crystallisation Methods 0.000 claims description 2
- 230000008025 crystallization Effects 0.000 claims description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 5
- 238000005192 partition Methods 0.000 description 5
- 206010037660 Pyrexia Diseases 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 235000011118 potassium hydroxide Nutrition 0.000 description 3
- NGHMEZWZOZEZOH-UHFFFAOYSA-N silicic acid;hydrate Chemical class O.O[Si](O)(O)O NGHMEZWZOZEZOH-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- WWGUMAYGTYQSGA-UHFFFAOYSA-N 2,3-dimethylnaphthalene Chemical compound C1=CC=C2C=C(C)C(C)=CC2=C1 WWGUMAYGTYQSGA-UHFFFAOYSA-N 0.000 description 2
- YGYNBBAUIYTWBF-UHFFFAOYSA-N 2,6-dimethylnaphthalene Chemical compound C1=C(C)C=CC2=CC(C)=CC=C21 YGYNBBAUIYTWBF-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- XYQRXRFVKUPBQN-UHFFFAOYSA-L Sodium carbonate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]C([O-])=O XYQRXRFVKUPBQN-UHFFFAOYSA-L 0.000 description 2
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- LVXHNCUCBXIIPE-UHFFFAOYSA-L disodium;hydrogen phosphate;hydrate Chemical compound O.[Na+].[Na+].OP([O-])([O-])=O LVXHNCUCBXIIPE-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- MFUVDXOKPBAHMC-UHFFFAOYSA-N magnesium;dinitrate;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MFUVDXOKPBAHMC-UHFFFAOYSA-N 0.000 description 2
- 229940018038 sodium carbonate decahydrate Drugs 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 2
- GXZZNUGESLEFGV-UHFFFAOYSA-N trioxomolybdenum;hydrate Chemical compound O.O=[Mo](=O)=O GXZZNUGESLEFGV-UHFFFAOYSA-N 0.000 description 2
- ZSQCNVWYBBKUHS-UHFFFAOYSA-N (2,3-dimethylphenyl)-phenylmethanone Chemical compound CC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1C ZSQCNVWYBBKUHS-UHFFFAOYSA-N 0.000 description 1
- CSVFWMMPUJDVKH-UHFFFAOYSA-N 1,1-dichloropropan-2-one Chemical compound CC(=O)C(Cl)Cl CSVFWMMPUJDVKH-UHFFFAOYSA-N 0.000 description 1
- ZMESHQOXZMOOQQ-UHFFFAOYSA-N 1-(naphthalen-1-ylmethyl)naphthalene Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZMESHQOXZMOOQQ-UHFFFAOYSA-N 0.000 description 1
- RZTDESRVPFKCBH-UHFFFAOYSA-N 1-methyl-4-(4-methylphenyl)benzene Chemical group C1=CC(C)=CC=C1C1=CC=C(C)C=C1 RZTDESRVPFKCBH-UHFFFAOYSA-N 0.000 description 1
- KZNJSFHJUQDYHE-UHFFFAOYSA-N 1-methylanthracene Chemical compound C1=CC=C2C=C3C(C)=CC=CC3=CC2=C1 KZNJSFHJUQDYHE-UHFFFAOYSA-N 0.000 description 1
- LRQYSMQNJLZKPS-UHFFFAOYSA-N 2,7-dimethylnaphthalene Chemical compound C1=CC(C)=CC2=CC(C)=CC=C21 LRQYSMQNJLZKPS-UHFFFAOYSA-N 0.000 description 1
- LUZDYPLAQQGJEA-UHFFFAOYSA-N 2-Methoxynaphthalene Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 description 1
- XNDZQQSKSQTQQD-UHFFFAOYSA-N 3-methylcyclohex-2-en-1-ol Chemical compound CC1=CC(O)CCC1 XNDZQQSKSQTQQD-UHFFFAOYSA-N 0.000 description 1
- ZHJGWYRLJUCMRT-UHFFFAOYSA-N 5-[6-[(4-methylpiperazin-1-yl)methyl]benzimidazol-1-yl]-3-[1-[2-(trifluoromethyl)phenyl]ethoxy]thiophene-2-carboxamide Chemical compound C=1C=CC=C(C(F)(F)F)C=1C(C)OC(=C(S1)C(N)=O)C=C1N(C1=C2)C=NC1=CC=C2CN1CCN(C)CC1 ZHJGWYRLJUCMRT-UHFFFAOYSA-N 0.000 description 1
- WPDAVTSOEQEGMS-UHFFFAOYSA-N 9,10-dihydroanthracene Chemical compound C1=CC=C2CC3=CC=CC=C3CC2=C1 WPDAVTSOEQEGMS-UHFFFAOYSA-N 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 1
- LTAFHSQYBZBQJQ-UHFFFAOYSA-L O.O.O.O.O.O.Br[Cu]Br Chemical compound O.O.O.O.O.O.Br[Cu]Br LTAFHSQYBZBQJQ-UHFFFAOYSA-L 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- QHFQAJHNDKBRBO-UHFFFAOYSA-L calcium chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Ca+2] QHFQAJHNDKBRBO-UHFFFAOYSA-L 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- QGUAJWGNOXCYJF-UHFFFAOYSA-N cobalt dinitrate hexahydrate Chemical compound O.O.O.O.O.O.[Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O QGUAJWGNOXCYJF-UHFFFAOYSA-N 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- VMKYLARTXWTBPI-UHFFFAOYSA-N copper;dinitrate;hydrate Chemical compound O.[Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O VMKYLARTXWTBPI-UHFFFAOYSA-N 0.000 description 1
- 150000004691 decahydrates Chemical class 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- DEOPWJHDYPLPRX-UHFFFAOYSA-M iron chloride hydrate Chemical compound O.[Cl-].[Fe] DEOPWJHDYPLPRX-UHFFFAOYSA-M 0.000 description 1
- SZQUEWJRBJDHSM-UHFFFAOYSA-N iron(3+);trinitrate;nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O SZQUEWJRBJDHSM-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- XEEYVTMVFJEEEY-UHFFFAOYSA-L magnesium;dichloride;tetrahydrate Chemical compound O.O.O.O.[Mg+2].[Cl-].[Cl-] XEEYVTMVFJEEEY-UHFFFAOYSA-L 0.000 description 1
- OQTQHQORDRKHFW-UHFFFAOYSA-L manganese(2+);sulfate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Mn+2].[O-]S([O-])(=O)=O OQTQHQORDRKHFW-UHFFFAOYSA-L 0.000 description 1
- CNFDGXZLMLFIJV-UHFFFAOYSA-L manganese(II) chloride tetrahydrate Chemical compound O.O.O.O.[Cl-].[Cl-].[Mn+2] CNFDGXZLMLFIJV-UHFFFAOYSA-L 0.000 description 1
- ISPYRSDWRDQNSW-UHFFFAOYSA-L manganese(II) sulfate monohydrate Chemical compound O.[Mn+2].[O-]S([O-])(=O)=O ISPYRSDWRDQNSW-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- LAIZPRYFQUWUBN-UHFFFAOYSA-L nickel chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Ni+2] LAIZPRYFQUWUBN-UHFFFAOYSA-L 0.000 description 1
- AOPCKOPZYFFEDA-UHFFFAOYSA-N nickel(2+);dinitrate;hexahydrate Chemical compound O.O.O.O.O.O.[Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O AOPCKOPZYFFEDA-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- -1 oxides Chemical class 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N trans-Stilbene Natural products C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【考案の詳細な説明】
〈産業上の利用分野〉
本考案は、例えば、保温剤,香料,その他薬剤
等の加熱揮散に用いられる新規な発熱構造体に関
する。更に詳しくは、特殊な容器と内容物(発熱
組成物)との組合せにより容易に一定温度に発熱
し得るようにした発熱構造物に関する。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a novel heat-generating structure used for heating and volatilizing heat insulating agents, fragrances, other drugs, etc., for example. More specifically, the present invention relates to a heat generating structure that can easily generate heat to a constant temperature by combining a special container and contents (heat generating composition).
〈従来技術及びその問題点〉
従来、酸化カルシウムの水和熱を利用した殺虫
剤,殺菌剤等の薬剤を加熱蒸散させる構造体に関
してはいくつかの提案がなされているが、これら
はいずれも酸化カルシウムに注水して発熱せしめ
るようにした構造体に関するものである。しか
し、このような外部からの注水を要する発熱体は
使用に不便であるばかりでなく、発熱温度の調整
も困難である。<Prior art and its problems> Several proposals have been made regarding structures that heat and evaporate chemicals such as insecticides and fungicides using the heat of hydration of calcium oxide, but none of these have been proposed. This relates to a structure that generates heat by injecting water into calcium. However, such a heating element that requires external water injection is not only inconvenient to use, but also difficult to adjust the temperature of the heat generated.
また、苛性ソーダ,苛性カリの粉粒体からなる
A成分と結晶水を有する硫酸塩の粉粒体からなる
B成分とを互いに接触しないよう内袋中に分割収
納して両成分の境界部を結束しておき、使用時に
結束部を解いて両成分を混合し、苛性ソーダ,苛
性カリの溶解発熱反応とそれに続く中和発熱反応
とによつて発熱させることも知られている。しか
し、苛性ソーダ,苛性カリは強度のアルカリ性を
有し取扱いに特別の注意を要するばかりでなく、
袋に収納された発熱剤を使用する際は、その都度
内袋を取出して結束部を解き、しかも、袋を手で
揉んでやる必要があり、使用上不便である。 In addition, component A, which consists of granules of caustic soda and caustic potash, and component B, which consists of granules of sulfate containing water of crystallization, are stored separately in an inner bag so that they do not come into contact with each other, and the boundary between the two components is tied together. It is also known that the binder is untied at the time of use, the two components are mixed, and heat is generated through an exothermic reaction of dissolution of caustic soda and caustic potash, followed by an exothermic reaction of neutralization. However, caustic soda and caustic potash not only have strong alkalinity and require special care when handling;
When using the exothermic agent stored in the bag, it is necessary to take out the inner bag, untie the binding, and rub the bag by hand each time, which is inconvenient in use.
〈考案の目的〉
本考案は、前述の如き問題がなく、注水や結束
部の解舒等を行なうことなく、ただ容器を回動さ
せて振るだけで容易に所定温度に発熱する発熱構
造体を提供することを目的とするものである。<Purpose of the invention> The present invention does not have the above-mentioned problems and provides a heat-generating structure that can easily generate heat to a predetermined temperature by simply rotating and shaking the container without having to pour water or unravel the binding part. The purpose is to provide
〈考案の構成〉
本考案は、前述の目的を達成するもので、二つ
の円筒状容器が同心的かつ回動自在に接合され、
両円筒状容器はそれぞれ接合部側の端面のほぼ半
分を開口部となして該容器の少くとも一方を回動
したとき接合部にほぼ半円形の連通孔が形成され
るように仕切られており、かつ、一方の容器には
(a)2〜80メツシユの粒度を有する酸化カルシウム
粉粒体が、他方の容器には(b)酸化カルシウムと接
触することによつて発熱する20メツシユより小さ
い粒度を有する常温で固体の結晶水含有化合物の
粉粒体が、さらに、一方もしくは両方の容器に(c)
前記両成分を接触させたときに発熱する最高温度
より低い温度で融解し、かつ前記(a),(b)両成分の
いずれとも反応しない常温で固体の化合物がそれ
ぞれ収納された発熱構造体である。<Structure of the invention> The present invention achieves the above-mentioned object. Two cylindrical containers are concentrically and rotatably joined,
Both cylindrical containers are partitioned so that approximately half of the end face on the joint side is an opening, and a substantially semicircular communication hole is formed at the joint when at least one of the containers is rotated. , and in one container
(a) Calcium oxide powder with a particle size of 2 to 80 meshes is placed in the other container, and (b) crystalline water, which is solid at room temperature and has a particle size smaller than 20 meshes, generates heat when it comes into contact with calcium oxide. Powder of the contained compound is further placed in one or both containers (c)
A heat-generating structure containing a compound that melts at a temperature lower than the maximum temperature that generates heat when the two components are brought into contact, and that is solid at room temperature and does not react with either of the components (a) and (b). be.
〈実施例〉
次に本考案の発熱構造体の一例を添付図面によ
り説明する。<Example> Next, an example of the heat generating structure of the present invention will be explained with reference to the accompanying drawings.
第1図は発熱構造体の断面図を示したものであ
り、第3図はその斜視図を示したものである。上
下に分かれた二つの円筒状容器1と2とは中央部
(接合部)を境にして回動出来るように同心状に
接合されており、接合部は、上の円筒状容器1に
おける半円形の下部仕切り板(底)2と下の円筒
状容器2における半円形の上部仕切り板(蓋)4
によつて仕切られている。そして上の容器中の収
納空間部分に斜線で示されているように、発熱体
の一方の成分である(a)酸化カルシウム粉粒体を、
下の容器中の収納空間部分にはもう一方の成分で
ある(b)酸化カルシウムと反応し発熱する作用を有
する常温で固体の結晶水化合物の粉粒体を、それ
ぞれ収納するとともに、上下いずれか一方の容器
または両方の容器に(c)前記(a),(b)両成分を接触さ
せたときに発熱する最高到達温度よりも低い温度
で融解し、かつ(a),(b)両成分のいずれとも反応し
ない常温で固体の化合物を収納しておく。この状
態ではたとえばこの容器を振つても成分(a)と(b)は
接触しないので長期の保存において両成分の性質
を損なうことがない。勿論上下の(a),(b)成分を逆
にして入れ替えてもよい。即ち上の容器中の収納
空間部分に(b)成分を、下の容器中の収納部分に(a)
成分を収納してもよい。また第1図の構造体の全
体を逆にして用いても何ら差支えない。 FIG. 1 shows a sectional view of the heat generating structure, and FIG. 3 shows a perspective view thereof. The two upper and lower cylindrical containers 1 and 2 are joined concentrically so that they can rotate with the center (joint) as the border, and the joint is a semicircular shape of the upper cylindrical container 1. A lower partition plate (bottom) 2 of the lower cylindrical container 2 and a semicircular upper partition plate (lid) 4 of the lower cylindrical container 2.
It is divided by. As shown by diagonal lines in the storage space in the upper container, (a) calcium oxide powder, which is one component of the heating element, is
The storage space in the lower container stores the other component (b) powder of a crystalline water compound that is solid at room temperature and has the effect of generating heat when it reacts with calcium oxide. (c) Both components (a) and (b) melt at a temperature lower than the maximum temperature that generates heat when they come into contact with one or both containers, and both components (a) and (b) Store a compound that is solid at room temperature and does not react with any of the following. In this state, even if the container is shaken, components (a) and (b) will not come into contact with each other, so the properties of both components will not be impaired during long-term storage. Of course, the upper and lower components (a) and (b) may be reversed and replaced. In other words, component (b) is placed in the storage space in the upper container, and component (a) is placed in the storage space in the lower container.
Components may be stored. Moreover, there is no problem even if the entire structure shown in FIG. 1 is used in reverse.
使用時においては、第2図に示されているよう
に、上の容器1或いは下の容器2または両方を回
動(約180゜回転)させることによつて半円状の仕
切り板3および4が重なり合い半円形の開口部が
形成され、該開口部を通じて上下の収納部分が連
通する。従つて、この状態で容器を上下に振るこ
とによつて、上の容器の空間部分に収納されてい
た成分(a)と下の容器の空間部分に収納されていた
成分(b)とが混合し接触して発熱を開始する。 In use, as shown in FIG. 2, the semicircular partition plates 3 and 4 are separated by rotating the upper container 1, the lower container 2, or both (about 180° rotation). overlap to form a semicircular opening, through which the upper and lower storage parts communicate. Therefore, by shaking the container up and down in this state, component (a) stored in the space in the upper container and component (b) stored in the space in the lower container are mixed. It starts to generate heat upon contact.
第4図は、第1図および第2図に示された上下
2つの容器の構造の理解を容易にするために分割
して示した斜視図であり、上下2つの部分は使用
前および使用中は第1図〜第3図の如く接合され
相互に回動できる構造になつている。 FIG. 4 is a perspective view showing the upper and lower containers shown in FIGS. are connected to each other as shown in FIGS. 1 to 3, so that they can rotate relative to each other.
本考案における(a)成分の酸化カルシウムはこの
粒度が2〜80メツシユ、好ましくは3〜20メツシ
ユのものが使用される。この範囲の粒度のものは
後述の(b)成分と混合したときに容易に発熱する。 The calcium oxide component (a) used in the present invention has a particle size of 2 to 80 mesh, preferably 3 to 20 mesh. Particles with a particle size within this range easily generate heat when mixed with component (b) described below.
もう一方の発熱成分である(b)成分の酸化カルシ
ウムと接触することにより発熱する常温で固体の
結晶水含有化合物の具体例としては、各種金属の
硫酸塩,硝酸塩,リン酸塩,炭酸塩,硅酸塩,ハ
ロゲン化物,酸化物,水酸化物等の中から選ばれ
る無機化合物の含水塩があげられる。かかる結晶
水含有化合物の好ましい具体例としては、硫酸ナ
トリウム10水和物[Na2 SO4・10H2O],硫酸マ
ンガン7水和物[MnSO4・7H2O],硫酸アルミ
ニウム含水塩[Al2(SO4)2・18H2O],硝酸カル
シウム4水和物[Ca(NO3)2・4H2O],硝酸アル
ミニウム9水和物[Al2(NO3)3・9H2O],硝酸マ
グネシウム6水和物[Mg(NO3)2・6H2O],硝酸
第2鉄9水和物[Fe(NO3)2・9H2O],硝酸ニツ
ケル6水和物[Ni(NO3)2・6H2O],硝酸コバル
ト6水和物[Co(NO3)2・6H2O],硝酸銅含水塩
[Cu(NO3)2・3H2O,Cu(NO3)2・6H2O],燐酸
水素ナトリウム含水塩[Na2 HPO4・12H2O],
炭酸ソーダ10水和物[Na2 CO3・10H2O],オル
ト硅酸[SiO2・2.5H2O・H4SiO4],ピロ硅酸
[SiO2・1.5H2O,SiO2・2.5H2O],メタ硅酸
[SiO2・0.5H2O]等の硅酸含水和物,塩化マグネ
シウム4水和物[MgCl2・4H2O],塩化カルシウ
ム6水和物[CaCl2・6H2O],塩化鉄含水塩
[FeCl2・4H2O,FeCl3・6H2O],塩化マンガン
4水和物[N Cl2・4H2O],塩化ニツケル6水
和物[NiCl2・6H2O],臭化銅6水和物
[CuBr2・6H2O],酸化モリブデン含水和物
[MoO3・2H2O]等があげられる。これらのう
ち、特に好ましい例としては、硫酸ナトリウム10
水和物,硅酸含水和物,炭酸ナトリウム10水和
物,燐酸水素ナトリウム含水和物,硫酸マンガン
含水物,硫酸アルミニウム含水和物,酸化モリブ
デン含水塩があげられ、とりわけ硫酸ナトリウム
10水和物,硅酸含水和物および炭酸ナトリウム10
水和物が安価で入手容易でもあり、最も好ましい
例である。 Specific examples of crystal water-containing compounds that are solid at room temperature and generate heat when they come into contact with calcium oxide, the other exothermic component (component (b)), include sulfates, nitrates, phosphates, carbonates of various metals, Examples include hydrated salts of inorganic compounds selected from silicates, halides, oxides, hydroxides, and the like. Preferred specific examples of such crystal water-containing compounds include sodium sulfate decahydrate [Na 2 SO 4 .10H 2 O], manganese sulfate heptahydrate [MnSO 4 .7H 2 O], aluminum sulfate hydrate [Al 2 (SO 4 ) 2・18H 2 O], calcium nitrate tetrahydrate [Ca(NO 3 ) 2・4H 2 O], aluminum nitrate nonahydrate [Al 2 (NO 3 ) 3・9H 2 O] , magnesium nitrate hexahydrate [Mg(NO 3 ) 2・6H 2 O], ferric nitrate nonahydrate [Fe(NO 3 ) 2・9H 2 O], nickel nitrate hexahydrate [Ni( NO 3 ) 2・6H 2 O], cobalt nitrate hexahydrate [Co(NO 3 ) 2・6H 2 O], copper nitrate hydrate [Cu(NO 3 ) 2・3H 2 O, Cu(NO 3 ) 2・6H 2 O], sodium hydrogen phosphate hydrate [Na 2 HPO 4・12H 2 O],
Sodium carbonate decahydrate [Na 2 CO 3・10H 2 O], orthosilicic acid [SiO 2・2.5H 2 O・H 4 SiO 4 ], pyrosilic acid [SiO 2・1.5H 2 O, SiO 2・2.5H 2 O], silicic acid hydrates such as meta-silicic acid [SiO 2・0.5H 2 O], magnesium chloride tetrahydrate [MgCl 2・4H 2 O], calcium chloride hexahydrate [CaCl 2・6H 2 O], iron chloride hydrate [FeCl 2・4H 2 O, FeCl 3・6H 2 O], manganese chloride tetrahydrate [N Cl 2・4H 2 O], nickel chloride hexahydrate [NiCl 2.6H 2 O], copper bromide hexahydrate [CuBr 2.6H 2 O], and molybdenum oxide hydrate [MoO 3.2H 2 O]. Among these, particularly preferred examples include sodium sulfate 10
hydrate, silicic acid hydrate, sodium carbonate decahydrate, sodium hydrogen phosphate hydrate, manganese sulfate hydrate, aluminum sulfate hydrate, molybdenum oxide hydrate, especially sodium sulfate.
decahydrate, silicic acid hydrate and sodium carbonate 10
Hydrates are the most preferred example because they are inexpensive and easily available.
一方、(b)成分はその粒度が20メツシユよりも小
さいもの、特に好ましくは30メツシユよりも小さ
いものが好適である。 On the other hand, component (b) preferably has a particle size smaller than 20 meshes, particularly preferably smaller than 30 meshes.
さらに、本考案では前記(c)成分が、前記(a)成分
あるいは(b)成分のいずれか、または(a)成分および
(b)成分の両者に混合されている。 Furthermore, in the present invention, the component (c) is either the component (a) or the component (b), or the component (a) and the component (b).
(b) is mixed with both components.
前記(c)成分は、(a)成分と(b)成分とを混合して接
触した場合、発熱する温度を制御し、所望の温度
に維持する作用を有している。かくして(c)成分を
(a)成分および/または(b)成分と予め混合してお
き、使用時に(a)成分と(b)成分とを混合すると、(c)
成分の化合物が融解する温度以上には温度が上昇
せず、ほぼ融解する温度に長時間維持することが
できる。従つてこの(c)成分は温度制御剤としての
作用を有するものである。 The component (c) has the function of controlling the temperature at which heat is generated and maintaining the temperature at a desired level when the components (a) and (b) are mixed and brought into contact. Thus, component (c)
If the components (a) and/or (b) are mixed in advance and the components (a) and (b) are mixed at the time of use, (c)
The temperature does not rise above the temperature at which the component compound melts, and can be maintained at approximately the melting temperature for a long time. Therefore, component (c) functions as a temperature control agent.
かかる(c)成分としては、40〜300℃の温度で融
解するものが好適であり、60〜250℃の温度で融
解するものが特に好ましい。(c)成分としては、無
機化合物,有機化合物のいずれであつてもよい
が、有機化合物が好ましい。適当な有機化合物と
しては、例えば炭化水素類,エステル類,エーテ
ル類,ケトン類があげられ、またこれらの他に高
分子重合体であつてもよい。 Component (c) is preferably one that melts at a temperature of 40 to 300°C, particularly preferably one that melts at a temperature of 60 to 250°C. Component (c) may be either an inorganic compound or an organic compound, but organic compounds are preferred. Suitable organic compounds include, for example, hydrocarbons, esters, ethers, and ketones, and in addition to these, high molecular weight polymers may also be used.
次にこれらの具体例をあげる。なおカツコの中
はそのものの融解温度(℃)を示すが、(c)成分と
して下記のものを使用した場合にはその融解温度
の近辺の温度に発熱温度を制御できるので、所望
の発熱温度により(c)成分を適宜選択すればよい。 Specific examples of these are given below. The inside of the cutlet indicates the melting temperature (℃) of the substance, but if the following is used as component (c), the exothermic temperature can be controlled to a temperature close to the melting temperature, so it can be adjusted according to the desired exothermic temperature. (c) Component may be selected appropriately.
(i) 炭化水素類:
例えば、トランススチルベン(124),クリセン
(225),アントラセン(216),9,10ジヒドロア
ントラセン(108),1−メチルアントラセン
(86),ジフエニル(70.5),4,4′−ジメチルジ
フエニル(125),ナフタリン(80),2,3−ジ
メチルナフタリン(104),2,6−ジメチルナフ
タリン(110),2,7−ジメチルナフタリン
(96),ジ−αナフチルメタン(109),アセナフテ
ン(95),
(ii) エステル類:
例えば、安息香酸フエニル(70),イソフタル
酸ジメチル(71),テレフタル酸ジメチル(141),
アセチル−4−ビフエニル(88),
(iii) エーテル類:
例えば、メチル−β−ナフチルエーテル(75),
(iv) ケトン類:
例えば、ジメチルベンゾフエノン(98),ジク
ロルアセトン(42),
これら(c)成分の粒度は、前記した(b)成分とほぼ
同じ範囲でよい。(i) Hydrocarbons: For example, transstilbene (124), chrysene (225), anthracene (216), 9,10 dihydroanthracene (108), 1-methylanthracene (86), diphenyl (70.5), 4,4 '-dimethyldiphenyl (125), naphthalene (80), 2,3-dimethylnaphthalene (104), 2,6-dimethylnaphthalene (110), 2,7-dimethylnaphthalene (96), di-α-naphthylmethane ( 109), acenaphthene (95), (ii) Esters: For example, phenyl benzoate (70), dimethyl isophthalate (71), dimethyl terephthalate (141),
Acetyl-4-biphenyl (88), (iii) Ethers: For example, methyl-β-naphthyl ether (75), (iv) Ketones: For example, dimethylbenzophenone (98), dichloroacetone (42), The particle size of these component (c) may be within approximately the same range as that of component (b) described above.
本考案において、(a)成分に対する(b)成分の量は
特に限定されるものではないが、(a)成分に対し(b)
成分があまりに少ないと発熱が困難となるか到達
する温度が低くなり経済的でなくなり、一方あま
りに多いと、同様に到達温度が低すぎることがあ
り、ある範囲の値であることが好ましい。例えば
(a)成分1モルに対し、(b)成分は10-8〜50モルの範
囲、好ましくは10-2〜30モルの範囲、特に好まし
くは2×10-2〜25モルの範囲がよい。 In the present invention, the amount of component (b) relative to component (a) is not particularly limited, but the amount of component (b) relative to component (a) is not particularly limited.
If the amount of the component is too small, it will be difficult to generate heat or the temperature reached will be low, making it uneconomical. On the other hand, if it is too large, the temperature reached will be too low, so a value within a certain range is preferable. for example
The amount of component (b) per mole of component (a) is in the range of 10 -8 to 50 moles, preferably in the range of 10 -2 to 30 moles, particularly preferably in the range of 2 x 10 -2 to 25 moles.
また(c)成分の割合は、(a)成分に対して重量で1/
5〜5倍、好ましくは1/4〜4倍、特に1/3〜3倍
の範囲が望ましい。 In addition, the ratio of component (c) is 1/1/by weight of component (a).
A range of 5 to 5 times, preferably 1/4 to 4 times, particularly 1/3 to 3 times is desirable.
また、本考案の発熱構造体は、用途によつて容
器の径や高さおよび大きさを任意に選択でき、ま
た構造体のある部分を伝熱面として利用し、残り
を保温して有効に用いることが有利である。例え
ば下の容器2の部分の底面あるいは側面等の外面
の一部あるいは全部を伝熱面として用い、上の容
器1の上面および側面を保温面として用いること
ができる。 In addition, the heat generating structure of the present invention allows the diameter, height, and size of the container to be arbitrarily selected depending on the application, and a certain part of the structure can be used as a heat transfer surface, and the rest can be effectively kept warm. It is advantageous to use For example, part or all of the outer surface such as the bottom or side surfaces of the lower container 2 can be used as a heat transfer surface, and the upper surface and side surfaces of the upper container 1 can be used as heat retention surfaces.
この例の如く伝熱面と保温面に分けて利用する
場合には容器1および2の材質等の選択や保温部
分に更に保温材を外側に用いることも任意である
が、いずれの場合も使用前後において容器1と2
は相互に回動できることが必要である。 When using the heat transfer surface and heat retention surface separately as in this example, it is optional to select the materials of containers 1 and 2, and to use heat insulating material on the outside of the heat retention part, but in either case, the Containers 1 and 2 in front and back
must be able to rotate relative to each other.
〈作用〉
本考案の発熱構造体において、保存時あるいは
輸送時等発熱を要しないときは、第1図および第
3図に示す如く、上下の容器が仕切られている状
態として、(a),(b)両成分が互いに接触しないよう
に保持し、使用時には、第2図の如く容器を回動
させて相対位置を約180゜変化させることにより、
両容器の接合部に半円状の連通孔を形成させる。
そして、この状態で、例えば数回上下に振ること
によつて、別々に収納されていた(a),(b),(c)各成
分が互いに均一にまざり合い、両成分の反応によ
つて発熱が生ずる。<Function> In the heat generating structure of the present invention, when heat generation is not required during storage or transportation, the upper and lower containers are separated as shown in Figs. 1 and 3, and (a), (b) Hold both components so that they do not come into contact with each other, and when in use, rotate the container to change the relative position by approximately 180° as shown in Figure 2.
A semicircular communication hole is formed at the joint of both containers.
In this state, for example, by shaking it up and down several times, the components (a), (b), and (c) that were stored separately will mix uniformly with each other, and the reaction between the two components will cause Fever occurs.
この場合、両成分の混合が容易に行われるため
には第1図および第2図に示されている如く円筒
状容器1および2に対して、それぞれの成分は(c)
成分を含めてある程度(例えば2割程度)の空間
を残して収納しておくことが望ましい。 In this case, in order to easily mix both components, each component should be (c) in cylindrical containers 1 and 2 as shown in FIGS.
It is desirable to leave a certain amount of space (for example, about 20%) including the ingredients when storing the items.
〈効果〉
本考案においては特定の粒度を有する(a)酸化カ
ルシウム粉末と(b)常温では固体の結晶水含有化合
物粉末とを混合することにより発熱が得られるた
め、注水や通気の必要もなく、使用時に容器を回
動させて振りまぜるだけで容易に発熱を得ること
ができる。しかも、前記(c)成分の種類をあらかじ
め選定することにより、発熱温度を任意に制御が
できる。また、本考案は各成分を使用前までは混
合しない様に上下別々の容器に収納しておき、使
用に際して、上述の如き極めて簡単な操作によつ
て2つの容器の内容物が相互に流通し、所定温度
に発熱する。<Effects> In the present invention, heat generation is obtained by mixing (a) calcium oxide powder with a specific particle size and (b) crystal water-containing compound powder that is solid at room temperature, so there is no need for water injection or ventilation. During use, heat can be easily generated by simply rotating and shaking the container. Moreover, by selecting the type of component (c) in advance, the exothermic temperature can be controlled arbitrarily. In addition, in this invention, each component is stored in separate containers at the top and bottom so that they are not mixed before use, and when used, the contents of the two containers can be mutually distributed by the extremely simple operation described above. , generates heat to a predetermined temperature.
かくして本考案の発熱構造体は、殺虫剤,殺菌
剤,誘引剤,殺鼠剤,殺ゴキブリ剤等、熱発散性
有害生物駆除剤等の加熱揮散用発熱体あるいは冷
凍食品の解凍,非常用あるいは携帯用の各種熱源
として利用できる。 Thus, the heat generating structure of the present invention can be used as a heating element for heating and volatilizing insecticides, bactericides, attractants, rodenticides, cockroach killers, etc., heat-dissipating pest control agents, etc., or for thawing frozen foods, emergency use, or portable use. It can be used as a variety of heat sources.
第1図および第2図はそれぞれ本考案の発熱構
造体の使用前および使用時の状態を示す断面図で
あり、第3図は第1図の構造体の斜視図、第4図
は第1図の構造体における上下の容器を分解した
斜視図である。
各図中、1は上方の円筒状容器、2は下方の円
筒状容器、3は上方の円筒状容器1の下部仕切り
板、4は下方の円筒状容器2の上部仕切り板、a
は発熱剤成分(a)、bは発熱剤成分(b)、cは発熱調
節剤成分(c)を示す。
1 and 2 are cross-sectional views showing the heat generating structure of the present invention before and during use, respectively, FIG. 3 is a perspective view of the structure shown in FIG. 1, and FIG. FIG. 3 is an exploded perspective view of the upper and lower containers in the illustrated structure. In each figure, 1 is the upper cylindrical container, 2 is the lower cylindrical container, 3 is the lower partition plate of the upper cylindrical container 1, 4 is the upper partition plate of the lower cylindrical container 2, a
represents the exothermic agent component (a), b represents the exothermic agent component (b), and c represents the exothermic agent component (c).
Claims (1)
れ、両円筒状容器はそれぞれ接合部側の端面のほ
ぼ半分を開口部となして該容器の少くとも一方を
回動したとき接合部にほぼ半円形の連通孔が形成
されるように仕切られており、かつ、一方の容器
には(a)2〜80メツシユの粒度を有する酸化カルシ
ウム粉粒体が、他方の容器には(b)酸化カルシウム
と接触することによつて発熱する20メツシユより
小さい粒度を有する常温で固体の結晶水含有化合
物の粉粒体が、さらに、一方もしくは両方の容器
に(c)前記両成分を接触させたときに発熱する最高
温度よりも低い温度で融解し、かつ前記(a)(b)両成
分のいずれとも反応しない常温で固体の化合物
が、それぞれ収納された発熱構造体。 Two cylindrical containers are concentrically and rotatably joined, and each cylindrical container has an opening in approximately half of the end face on the joint side, and when at least one of the containers is rotated, approximately half of the end face on the joint side is opened. It is partitioned to form a semicircular communication hole, and one container contains (a) calcium oxide powder with a particle size of 2 to 80 mesh, and the other container contains (b) calcium oxide powder. When the granular material of a compound containing water of crystallization, which is solid at room temperature and has a particle size of less than 20 meshes and which generates heat when it comes into contact with calcium, is further brought into contact with one or both containers of (c) both of the above components. A heat-generating structure containing a compound that melts at a temperature lower than the maximum temperature at which heat is generated and is solid at room temperature and does not react with either of the components (a) and (b).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1979113980U JPS6329728Y2 (en) | 1979-08-21 | 1979-08-21 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1979113980U JPS6329728Y2 (en) | 1979-08-21 | 1979-08-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5631548U JPS5631548U (en) | 1981-03-27 |
JPS6329728Y2 true JPS6329728Y2 (en) | 1988-08-09 |
Family
ID=29346248
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1979113980U Expired JPS6329728Y2 (en) | 1979-08-21 | 1979-08-21 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6329728Y2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4935282A (en) * | 1972-08-07 | 1974-04-01 | ||
JPS53528U (en) * | 1976-06-17 | 1978-01-06 |
-
1979
- 1979-08-21 JP JP1979113980U patent/JPS6329728Y2/ja not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4935282A (en) * | 1972-08-07 | 1974-04-01 | ||
JPS53528U (en) * | 1976-06-17 | 1978-01-06 |
Also Published As
Publication number | Publication date |
---|---|
JPS5631548U (en) | 1981-03-27 |
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