JPH0523504Y2 - - Google Patents
Info
- Publication number
- JPH0523504Y2 JPH0523504Y2 JP18841087U JP18841087U JPH0523504Y2 JP H0523504 Y2 JPH0523504 Y2 JP H0523504Y2 JP 18841087 U JP18841087 U JP 18841087U JP 18841087 U JP18841087 U JP 18841087U JP H0523504 Y2 JPH0523504 Y2 JP H0523504Y2
- Authority
- JP
- Japan
- Prior art keywords
- water
- container
- drug
- endothermic reaction
- drugs
- 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 - Lifetime
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 43
- 239000003814 drug Substances 0.000 claims description 38
- 229940079593 drug Drugs 0.000 claims description 36
- 238000001816 cooling Methods 0.000 claims description 15
- 239000012528 membrane Substances 0.000 claims description 13
- 238000000926 separation method Methods 0.000 claims description 13
- 238000005192 partition Methods 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- DBTMGCOVALSLOR-UHFFFAOYSA-N 32-alpha-galactosyl-3-alpha-galactosyl-galactose Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(OC2C(C(CO)OC(O)C2O)O)OC(CO)C1O DBTMGCOVALSLOR-UHFFFAOYSA-N 0.000 claims description 2
- RXVWSYJTUUKTEA-UHFFFAOYSA-N D-maltotriose Natural products OC1C(O)C(OC(C(O)CO)C(O)C(O)C=O)OC(CO)C1OC1C(O)C(O)C(O)C(CO)O1 RXVWSYJTUUKTEA-UHFFFAOYSA-N 0.000 claims description 2
- 150000004676 glycans Chemical class 0.000 claims description 2
- FYGDTMLNYKFZSV-UHFFFAOYSA-N mannotriose Natural products OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(OC2C(OC(O)C(O)C2O)CO)C(O)C1O FYGDTMLNYKFZSV-UHFFFAOYSA-N 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 229920001282 polysaccharide Polymers 0.000 claims description 2
- 239000005017 polysaccharide Substances 0.000 claims description 2
- 239000002195 soluble material Substances 0.000 claims description 2
- FYGDTMLNYKFZSV-BYLHFPJWSA-N β-1,4-galactotrioside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@H](CO)O[C@@H](O[C@@H]2[C@@H](O[C@@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-BYLHFPJWSA-N 0.000 claims description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 229920001218 Pullulan Polymers 0.000 description 3
- 239000004373 Pullulan Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000019423 pullulan Nutrition 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Packages (AREA)
- Cookers (AREA)
Description
<産業上の利用分野>
本考案は、物理化学的な吸熱反応を利用して、
必要時に飲食物等を短時間のうちに冷却すること
のできる冷却容器に関するものである。
<従来の技術>
従来の冷却容器において、反応水に加えて吸熱
反応を起こさせて使用される薬剤は、硝酸アンモ
ニウムと尿素の混合体あるいは硝酸アンモニウム
と塩化アンモニウムの混合体が知られている。
これらの薬剤は単独で用いられる場合もある
が、上述のように2種以上を併用することにより
冷却効果が上がる場合があり、よく用いられてい
た。
<考案が解決しようとする問題点>
しかしながら、硝酸アンモニウムと有機物を粉
体状態、顆粒状態で混合しておくと、爆発の可能
性があるため危険性が知られている。
また、薬剤の組み合わせ方によつては、2種の
薬剤が直接接する状態で高温保存した場合、薬剤
同士が反応乃至変質することが実験により判明し
た。
<問題点を解決するための手段>
本考案は以上の事情に鑑み検討がなされたもの
であつて、被冷却物である食品等を、薬剤が水へ
溶解する際の吸熱反応を利用して冷却するよう
に、吸熱反応室と被冷却物収容室の2室を持つ構
造の冷却容器において、吸熱反応室には外圧を加
えることにより水容器を破壊する手段を有する水
容器および2種以上の薬剤を区画して収容し、さ
らに、該2種以上の薬剤を2以上に区画する、水
溶性材料からなる分離膜を設けたことを特徴とす
る冷却容器であり、保存時には各薬剤同士が接触
しないように構成したものである。
<作用>
本考案の冷却容器は適宜手段例えば外圧を水容
器に伝達する機構に人為的に加圧することにより
水容器を破壊させ反応水を流出させて薬剤の周囲
を反応水で満たすことにより、薬剤を区画する分
離膜が取り除かれ、薬剤と反応水が混合されこの
とき初めて吸熱反応が起きる。
<実施例>
以下図面を参照して本考案を詳細に説明する。
第1図は本考案の冷却容器の1実施例を示す断面
図である。
容器本体9の内部は薬剤容器8で2室に区切ら
れている。この両者は端部で互いに巻締めること
により固定されている。薬剤容器8の外側部分と
容器本体9に囲まれる空間には、内容物11が充
填されている。薬剤容器8の内部には反応水7と
反応して吸熱反応を起こす2種以上の薬剤10が
分離膜12でそれぞれ区画されて収納されてい
る。この2種以上の薬剤10の上には反応水7の
入つた水容器5が収容され、蓋2により薬剤容器
8は封止されている。さらに、蓋2上には、取り
はずし可能な保護キヤツプ1が設けられている。
容器本体9は、紙、金属、プラスチツクあるい
はこれらの複合材料からなる筒状体である。また
薬剤容器8は後述する吸熱反応による熱が内容物
11と交換され易いよう金属製の物を用いる。薬
剤容器8内には反応水7と混合することにより、
吸熱反応を生じる2種以上の薬剤10が収納さ
れ、各薬剤10は互いに直接接触しないように分
離膜12で区画されている。薬剤10としては、
硝酸アンモニウム、尿素、塩化アンモニウム等の
公知の材料を、要求される反応温度に応じて任意
の割合に調整して用いる。分離膜12としては少
なくとも易水溶性であり、好ましくは10℃以下の
低温時においても水に可溶な材料を用いる。具体
的には、ポリビニルアルコール等の水溶性樹脂、
あるいはマルトトリオースがα−1,6結合した
中性単純多糖類(以下プルランと呼ぶ)が使用可
能である。特にこのプルランは、低温時でも容易
に水に溶けるので好ましい。2種以上の薬剤10
をそれぞれ区画するには、図示の如く各薬剤10
の少なくとも一種を前述の分離膜12にて包装す
るか、あるいは薬剤10を層状に設け各薬剤10
層間に分離膜12を隔壁として設けてもよい。い
ずれにしても、各薬剤10が直接接触しない状態
に分離膜12を設けることが必要である。水容器
5は適宜手段により破壊され反応水7が流出する
構造となつており、第1図の実施例においては、
天面3が外部操作により凸状から凹状へ変位する
ことが可能な構造を持ち、その反対側の開口部は
封止部材6により封止されており、その天面3に
柱状の破壊部材4が水容器5の中心に向かつて傾
斜した形で設けられてなる水容器5である。第2
図は第1図の実施例の使用状態を示したものであ
る。まず、蓋2は中へ押し込まれることにより凸
状から凹状へ変形する。そして水容器5の天面3
もそれに応じて同様に変形する。すると柱状の破
壊部材4は天面3が凸状から凹状へ変形するのに
応じて扇形に広がり、かつ破壊部材4の先端部
4′は封止部材6よりも下方に突出するため、封
止部材6は大きく開裂し、水容器5中の反応水7
は薬剤10の上に注がれる。反応水7が注がれる
と薬剤10を包んでいた分離膜12は溶解するた
め、反応水7と薬剤10が混合する。この後必要
に応じて振盪撹拌することにより吸熱反応が始ま
る。この冷却反応により内容物11は薬剤容器8
の壁を介して冷却される。
本考案において水容器5の構造、即ち反応水7
を流出させる方法は、上記実施例に限らず任意で
あり、たとえば水容器5の可動な内天面にピンを
設けて封止部材6を穿孔する構造や、別体のピン
を準備し、容器外部よりピンを突き刺して水容器
(水袋)5を破壊するようにしてもよい。
<試験例>
薬剤の高温保存性およびその後の冷却能力を測
定するために、以下の実験を行つた。
薬剤として、硝酸アンモニウムおよび尿素を各
40g準備し、硝酸アンモニウムをプルランにて包
装し、金属容器中に上記薬剤を収納し密封した。
その後上記試験品を、20℃、40℃、60℃の各定温
室に24時間保存した。試験品を室温まで徐冷し、
反応水として20℃の純水80gを加え、撹拌した後
この金属容器を、20℃の水200gを収納したプラ
スチツク容器中に投じ、水を冷却した。冷却され
た水の温度を経時的に測定した。
比較例として、硝酸アンモニウム単体80g(比
較例1)、尿素単体80g(比較例2)、硝酸アンモ
ニウム40gと尿素40gを混合した薬剤(比較例
3)をそれぞれ準備し、同様の実験を行つた。結
果を表に示す。
<Industrial Application Field> This invention utilizes a physicochemical endothermic reaction,
The present invention relates to a cooling container that can cool food and drinks in a short time when necessary. <Prior Art> In conventional cooling containers, a mixture of ammonium nitrate and urea or a mixture of ammonium nitrate and ammonium chloride is known as a chemical used in addition to reaction water to cause an endothermic reaction. These agents may be used alone, but as mentioned above, the cooling effect may be enhanced by using two or more in combination, and they have often been used. <Problems to be solved by the invention> However, mixing ammonium nitrate and organic substances in powder or granule form is known to be dangerous as it may cause an explosion. Furthermore, it has been found through experiments that depending on the combination of drugs, if two types of drugs are stored at high temperatures in direct contact with each other, the drugs may react with each other or change in quality. <Means for Solving the Problems> The present invention was developed in view of the above circumstances, and uses an endothermic reaction to cool the object, such as food, by utilizing the endothermic reaction when the drug dissolves in water. In a cooling container having two chambers, an endothermic reaction chamber and a cooling object storage chamber, the endothermic reaction chamber includes a water container having a means for destroying the water container by applying external pressure, and two or more types of cooling containers. A cooling container that compartmentally stores drugs and is further equipped with a separation membrane made of a water-soluble material that partitions the two or more drugs into two or more, so that the drugs do not come into contact with each other during storage. It is configured so that it does not occur. <Function> The cooling container of the present invention can be used by appropriate means, such as artificially pressurizing the mechanism that transmits external pressure to the water container, thereby destroying the water container and causing the reaction water to flow out, filling the area around the drug with the reaction water. The separation membrane that partitions the drug is removed, the drug and reaction water are mixed, and only then does an endothermic reaction occur. <Example> The present invention will be described in detail below with reference to the drawings.
FIG. 1 is a sectional view showing one embodiment of the cooling container of the present invention. The inside of the container body 9 is divided into two chambers by the medicine container 8. These two parts are fixed by winding them together at their ends. A space surrounded by the outer portion of the drug container 8 and the container body 9 is filled with contents 11 . Inside the drug container 8, two or more types of drugs 10 that react with the reaction water 7 to cause an endothermic reaction are stored and separated by separation membranes 12, respectively. A water container 5 containing reaction water 7 is housed above the two or more types of chemicals 10, and the medicine container 8 is sealed with a lid 2. Furthermore, a removable protective cap 1 is provided on the lid 2. The container body 9 is a cylindrical body made of paper, metal, plastic, or a composite material thereof. Further, the drug container 8 is made of metal so that heat due to an endothermic reaction, which will be described later, can be easily exchanged with the contents 11. By mixing with the reaction water 7 in the drug container 8,
Two or more types of drugs 10 that cause an endothermic reaction are housed, and each drug 10 is separated by a separation membrane 12 so as not to come into direct contact with each other. As drug 10,
Known materials such as ammonium nitrate, urea, ammonium chloride, etc. are used in arbitrary proportions depending on the required reaction temperature. The separation membrane 12 is made of a material that is at least easily soluble in water, and preferably soluble in water even at low temperatures of 10° C. or lower. Specifically, water-soluble resins such as polyvinyl alcohol,
Alternatively, a neutral simple polysaccharide (hereinafter referred to as pullulan) in which maltotriose is linked with α-1,6 bonds can be used. Particularly, this pullulan is preferable because it easily dissolves in water even at low temperatures. 2 or more types of drugs 10
In order to separate each drug 10 as shown in the figure,
At least one of the above is packaged with the above-mentioned separation membrane 12, or the drugs 10 are arranged in layers, and each drug 10 is packaged with the separation membrane 12 described above.
A separation membrane 12 may be provided between the layers as a partition wall. In any case, it is necessary to provide the separation membrane 12 in a state where the respective drugs 10 do not come into direct contact with each other. The water container 5 is constructed to be destroyed by appropriate means and the reaction water 7 flows out, and in the embodiment shown in FIG.
The top surface 3 has a structure that can be displaced from a convex shape to a concave shape by external operation, the opening on the opposite side is sealed with a sealing member 6, and a column-shaped breakable member 4 is attached to the top surface 3. The water container 5 is provided in an inclined manner toward the center of the water container 5. Second
The figure shows the state in which the embodiment of FIG. 1 is used. First, the lid 2 is deformed from a convex shape to a concave shape by being pushed inside. and the top surface 3 of the water container 5
is similarly transformed accordingly. Then, as the top surface 3 deforms from a convex shape to a concave shape, the columnar destructive member 4 spreads out in a fan shape, and the tip 4' of the destructive member 4 protrudes below the sealing member 6. The member 6 is greatly cleaved, and the reaction water 7 in the water container 5 is released.
is poured onto the drug 10. When the reaction water 7 is poured, the separation membrane 12 surrounding the drug 10 is dissolved, so that the reaction water 7 and the drug 10 are mixed. After this, an endothermic reaction is started by shaking and stirring as necessary. Due to this cooling reaction, the contents 11 are transferred to the drug container 8.
cooled through the walls of the In the present invention, the structure of the water container 5, that is, the reaction water 7
The method for draining water is not limited to the above-mentioned embodiments, but may be arbitrary. For example, a pin may be provided on the movable inner top surface of the water container 5 to pierce the sealing member 6, or a separate pin may be prepared to drain the water from the container. The water container (water bag) 5 may be destroyed by piercing a pin from the outside. <Test Example> The following experiment was conducted to measure the high temperature storage stability and subsequent cooling ability of the drug. Ammonium nitrate and urea are used as drugs.
40g of ammonium nitrate was prepared, packaged with pullulan, and the drug was placed in a metal container and sealed.
Thereafter, the above test products were stored in constant temperature chambers at 20°C, 40°C, and 60°C for 24 hours. Slowly cool the test item to room temperature,
After adding 80 g of pure water at 20° C. as reaction water and stirring, the metal container was poured into a plastic container containing 200 g of water at 20° C., and the water was cooled. The temperature of the cooled water was measured over time. As comparative examples, 80 g of ammonium nitrate alone (Comparative Example 1), 80 g of urea alone (Comparative Example 2), and a mixture of 40 g of ammonium nitrate and 40 g of urea (Comparative Example 3) were prepared and similar experiments were conducted. The results are shown in the table.
【表】
<考案の効果>
本考案は以上述べた構成からなつているので、
使用前には薬剤が相互に接触しておらず爆発する
恐れはなく、さらに薬剤が変質することもないの
で使用時には所定の吸熱反応を生じ内容物を適切
に冷却することができ実用上優れた冷却容器であ
る。[Table] <Effects of the invention> Since the invention consists of the above-mentioned configuration,
Before use, the drugs do not come into contact with each other, so there is no risk of explosion, and since the drugs do not change in quality, a predetermined endothermic reaction occurs during use, allowing the contents to be cooled appropriately, which is excellent in practical use. It is a cooling container.
第1図は本考案の一実施例を示す断面図、第2
図は同実施例の使用状態を示す断面図である。
3……天面、4……破壊部材、5……水容器、
6……封止部材、7……反応水、8……薬剤容
器、9……容器本体、10……薬剤、11……内
容物、12……分離膜。
Fig. 1 is a sectional view showing one embodiment of the present invention;
The figure is a sectional view showing the usage state of the same embodiment. 3...Top surface, 4...Destructible member, 5...Water container,
6... Sealing member, 7... Reaction water, 8... Drug container, 9... Container body, 10... Drug, 11... Contents, 12... Separation membrane.
Claims (1)
る際の吸熱反応を利用して冷却するように、吸
熱反応室と被冷却物収容室の2室を持つ構造の
冷却容器において、吸熱反応室には外圧を加え
ることにより水容器を破壊する手段を有する水
容器および2種以上の薬剤を区画して収容し、
さらに、該2種以上の薬剤を2以上に区画す
る、水溶性材料からなる分離膜を設けたことを
特徴とする冷却容器。 2 前記分離膜は、マルトトリオースがα−1,
6結合した中性単純多糖類からなるフイルムで
あることを特徴とする、実用新案登録請求の範
囲第1項に記載の冷却容器。[Claims for Utility Model Registration] 1. Two chambers, an endothermic reaction chamber and a storage chamber for objects to be cooled, are designed to cool objects to be cooled, such as food, by utilizing an endothermic reaction when a drug is dissolved in water. In the cooling container having a structure in which the endothermic reaction chamber contains a water container having means for destroying the water container by applying external pressure and two or more types of chemicals, the water container is partitioned and accommodated;
A cooling container further comprising a separation membrane made of a water-soluble material that partitions the two or more types of drugs into two or more. 2 In the separation membrane, maltotriose is α-1,
The cooling container according to claim 1, which is a film made of a neutral simple polysaccharide having six bonds.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18841087U JPH0523504Y2 (en) | 1987-12-11 | 1987-12-11 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18841087U JPH0523504Y2 (en) | 1987-12-11 | 1987-12-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0191776U JPH0191776U (en) | 1989-06-15 |
| JPH0523504Y2 true JPH0523504Y2 (en) | 1993-06-16 |
Family
ID=31479506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18841087U Expired - Lifetime JPH0523504Y2 (en) | 1987-12-11 | 1987-12-11 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0523504Y2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0621411Y2 (en) * | 1989-11-06 | 1994-06-08 | 大和製罐株式会社 | Container with heating function |
| US20100206889A1 (en) * | 2007-07-13 | 2010-08-19 | Fast Drinks 2005, S.L | Self-heatable container |
| JP2020172289A (en) * | 2019-04-10 | 2020-10-22 | シーバイエス株式会社 | Drug container |
-
1987
- 1987-12-11 JP JP18841087U patent/JPH0523504Y2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0191776U (en) | 1989-06-15 |
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