JPS6340456B2 - - Google Patents
Info
- Publication number
- JPS6340456B2 JPS6340456B2 JP58090995A JP9099583A JPS6340456B2 JP S6340456 B2 JPS6340456 B2 JP S6340456B2 JP 58090995 A JP58090995 A JP 58090995A JP 9099583 A JP9099583 A JP 9099583A JP S6340456 B2 JPS6340456 B2 JP S6340456B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- hydrogel
- water
- aluminate
- silicates
- 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 27
- 150000003839 salts Chemical class 0.000 claims description 23
- 239000000499 gel Substances 0.000 claims description 13
- 239000000017 hydrogel Substances 0.000 claims description 13
- 150000004645 aluminates Chemical class 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- 230000003472 neutralizing effect Effects 0.000 claims description 8
- 229910001388 sodium aluminate Inorganic materials 0.000 claims description 8
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- 150000004760 silicates Chemical class 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 239000003456 ion exchange resin Substances 0.000 claims description 6
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 6
- 239000004115 Sodium Silicate Substances 0.000 claims description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- 239000004111 Potassium silicate Substances 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
- -1 aluminate salts Chemical class 0.000 claims description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
- 239000003729 cation exchange resin Substances 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 claims description 2
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052912 lithium silicate Inorganic materials 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 2
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 2
- 235000019353 potassium silicate Nutrition 0.000 claims description 2
- KVOIJEARBNBHHP-UHFFFAOYSA-N potassium;oxido(oxo)alumane Chemical compound [K+].[O-][Al]=O KVOIJEARBNBHHP-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 239000011259 mixed solution Substances 0.000 claims 3
- 150000001447 alkali salts Chemical class 0.000 claims 2
- 229940023913 cation exchange resins Drugs 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 238000005338 heat storage Methods 0.000 description 10
- 238000001879 gelation Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 239000011232 storage material Substances 0.000 description 8
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 7
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 6
- 230000005855 radiation Effects 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000013505 freshwater Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000004397 blinking Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Landscapes
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Description
【発明の詳細な説明】
本発明は新しい蓄熱材料として包水ゲルを用い
たソーラポンドに関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a solar pond using hydrogel as a new heat storage material.
ソーラポンドとは太陽光を熱の形で吸収し、貯
蔵することができる池のことである。 A solar pond is a pond that can absorb and store sunlight in the form of heat.
従来のソーラポンドの集熱および蓄熱の特徴は
対流を防止する非対流層を形成し、放熱を抑制す
ることである。放熱を抑制するには塩類の濃度勾
配を作り、この濃度勾配による密度差で温度差に
よる密度差の発生を防止し、これによつて浮力に
よる対流の発生を防止すればよい。対流が防止さ
れれば放熱が抑制され、長期の蓄熱が可能とな
る。 The heat collection and storage feature of conventional solar ponds is that they form a non-convection layer that prevents convection and suppresses heat radiation. To suppress heat radiation, a concentration gradient of salts is created, and the density difference due to this concentration gradient prevents the occurrence of a density difference due to a temperature difference, thereby preventing the occurrence of convection due to buoyancy. If convection is prevented, heat radiation is suppressed and long-term heat storage becomes possible.
しかしながら塩類水のソーラポンドでは次に記
すような欠点がある。濃度勾配の作製には濃塩類
溶液の上層部に真水を流して濃度勾配を強制的に
形成することにより、上層部が希薄な塩溶液にな
るため、上層部では対流が起り常に真水を流して
おく必要があるので保守管理に経費と手数が必要
である。この塩類水ポンドは塩類水勾配の形成が
成立するまでにかなりの日数を要し蓄熱を開始す
るまでに数ケ月の期間がかかる。また少量の漏水
でも濃厚塩水であるため魚の孵化や養殖などの塩
害が致命的な場所には使用できない。さらに塩類
水の濃度は20%以上にしなければ対流が防止でき
ないので大量の塩類が必要であり経済的にも不利
である。塩類の内、硼酸ナトリウムのように長期
間使用すると塩が沈降し底部が白くなる欠点があ
るものもある。また蓄熱量は比熱と温度および質
量の積によつて表わされるが、水の比熱が一番大
きく、塩類は比較的小さいので、水単独の熱量が
一番大きく、塩類の濃度が増加するにつれて減少
する。密度勾配法による塩類ソーラポンドの熱量
は濃厚塩類水溶液のため、低濃度塩類水溶液と比
較すると同温、同質量の場合では低濃度の塩類水
溶液の方が大きい。それ故濃厚塩水ソーラポンド
は効率が悪い方法といえる。また藻、泥や砂など
が混入した場合には大量の濃厚塩類水のため、塩
害が起るなどして投棄できないなどの欠点があ
る。 However, saline water solar ponds have the following drawbacks. To create a concentration gradient, fresh water is forced into the upper layer of a concentrated salt solution to forcibly form a concentration gradient, resulting in a dilute salt solution in the upper layer.Convection occurs in the upper layer and fresh water is constantly flowing. Therefore, maintenance and management costs and effort are required. This salt water pond takes a considerable number of days to form a salt water gradient and several months to start storing heat. In addition, even a small amount of water leakage results in highly concentrated salt water, so it cannot be used in areas where salt damage is fatal, such as when hatching or cultivating fish. Furthermore, since convection cannot be prevented unless the concentration of salt water is 20% or more, a large amount of salt is required, which is economically disadvantageous. Some salts, such as sodium borate, have the disadvantage that if used for a long period of time, the salt will settle and the bottom will turn white. Also, the amount of heat stored is expressed as the product of specific heat, temperature, and mass, but the specific heat of water is the largest, and since salts are relatively small, the amount of heat stored in water alone is the largest, and decreases as the concentration of salts increases. do. The calorific value of a salt solar pond determined by the density gradient method is a concentrated salt aqueous solution, so compared to a low concentration salt aqueous solution, a low concentration salt aqueous solution is larger at the same temperature and mass. Therefore, concentrated salt water solar ponds can be said to be an inefficient method. Furthermore, if algae, mud, or sand is mixed in, the large amount of concentrated saline water can cause salt damage and cannot be dumped.
本発明は上記欠点を種々考慮して、大量の集熱
蓄熱可能なソーラポンド用蓄熱材料を鋭意研究し
た結果、全く新しいソーラポンド用蓄熱材料とし
てゲル状物質を用いることにより、その目的を達
成しうることを見出し、この知見に基づいて本発
明に至つた。 The present invention has been made as a result of intensive research into a heat storage material for solar ponds that can collect and store a large amount of heat, taking into consideration the various drawbacks mentioned above, and has found that the purpose can be achieved by using a gel-like material as a completely new heat storage material for solar ponds. Based on this finding, we have arrived at the present invention.
本発明はケイ酸塩類にアルミン酸塩類を溶解し
た水溶液を酸により中和してゲル状物質を生成せ
しめ、これをソーラポンドの蓄熱材料として用い
るもので、蓄熱効率を従来の塩類水ソーラポンド
より大巾に改善することを特徴とする蓄熱材料を
提供するものである。 The present invention neutralizes an aqueous solution of aluminates in silicates with acid to generate a gel-like substance, which is used as a heat storage material for solar ponds.The heat storage efficiency is much greater than that of conventional salt water solar ponds. The present invention provides a heat storage material characterized by improved properties.
本発明の蓄熱材料について、さらに詳しく記
す。先づ原料のケイ酸塩類であるケイ酸ナトリウ
ム、ケイ酸カリウムおよびケイ酸リチウムは粉末
でも濃厚溶液(アメ状)でもよく、またアルミン
酸ナトリウム、アルミン酸カリウムおよびアルミ
ン酸リチウムは粉末状でも溶液でもよい。中和剤
としての酸類は塩酸、硫酸、硝酸あるいは酢酸、
コハク酸、クエン酸、フマル酸などである。中和
剤としてのイオン交換樹脂は弱酸性、強酸性陽イ
オン交換樹脂ならばいずれのものでもよい。 The heat storage material of the present invention will be described in more detail. First, the raw silicates, sodium silicate, potassium silicate, and lithium silicate, may be in powder or concentrated solution (candy-like), and sodium aluminate, potassium aluminate, and lithium aluminate may be in powder form or solution. good. Acids used as neutralizing agents include hydrochloric acid, sulfuric acid, nitric acid, or acetic acid;
These include succinic acid, citric acid, and fumaric acid. The ion exchange resin used as the neutralizing agent may be any weakly acidic or strongly acidic cation exchange resin.
ゲル生成の反応条件および蓄熱材料としての最
適条件を記すと、ゲルの生成はケイ酸塩とアルミ
ン酸塩を溶解したのち、酸やイオン交換樹脂を加
えて中和すれば、水を多量に含んだ、いわゆる包
水ゲルが生成する。ケイ酸塩単独の場合よりアル
ミン酸塩を添加した場合の方がゲル化時間が速く
なる。経済的にはゲル化時間が速く、なおかつ、
低濃度で流動性が起らないようなケイ酸塩および
アルミン酸塩の濃度が望ましい。通常用いられる
ケイ酸塩濃度としては0.1%から10%が、またア
ルミン酸塩濃度としてはケイ酸塩の重量に対して
0.1%か30%が最適である。 Regarding the reaction conditions for gel formation and the optimal conditions for use as a heat storage material, gels can be formed by dissolving silicate and aluminate and then neutralizing them by adding acid or ion exchange resin, which contains a large amount of water. A so-called hydrogel is produced. The gelation time is faster with the addition of aluminate than with silicate alone. Economically, the gelation time is fast, and
Concentrations of silicates and aluminates such that flowability does not occur at low concentrations are desirable. The commonly used silicate concentrations are 0.1% to 10%, and the aluminate concentrations are based on the weight of the silicate.
0.1% or 30% is optimal.
中和する条件としては、酸やイオン交換樹脂な
どの種類によつて、濃度や量が異なるが、通常の
中和条件は水素イオン濃度が6〜8の間が適当で
ある。溶液がゲル状になるいわゆるゲル化時間は
水素イオン濃度で決まるが、ケイ酸塩単独に比較
してアルミン酸塩を添加した場合には水素イオン
濃度の広い範囲でゲル化が起るし、そのゲル化時
間も速い。たとえば5%のケイ酸ナトリウムと1
%のアルミン酸ナトリウムとの混合溶液を50%の
硫酸で水素イオン濃度6.0に中和したとき、5分
でゲル化が始まり、30分で完結する。アルミン酸
ナトリウムがケイ酸ナトリウムに対して増加する
に従つてゲル化時間が速くなるし、またゲル化す
る水素イオン濃度の範囲はアルミン酸ナトリウム
の増加に従つて広がる。ゲル化に使用する酸やイ
オン交換樹脂は要求されるゲル化速度にしたがつ
て選択すればよく、簡単に大量の包水ゲルを製造
することができる。 Although the concentration and amount of neutralizing conditions vary depending on the type of acid and ion exchange resin, the normal neutralizing condition is a hydrogen ion concentration of 6 to 8. The so-called gelation time when a solution becomes gel-like is determined by the hydrogen ion concentration, but gelation occurs over a wider range of hydrogen ion concentrations when aluminate is added compared to silicate alone. Gel time is also fast. For example, 5% sodium silicate and 1
% sodium aluminate is neutralized with 50% sulfuric acid to a hydrogen ion concentration of 6.0, gelation begins in 5 minutes and completes in 30 minutes. As the amount of sodium aluminate increases relative to the amount of sodium silicate, the gelation time becomes faster, and the range of hydrogen ion concentrations at which gelation occurs widens as the amount of sodium aluminate increases. The acid and ion exchange resin used for gelation can be selected according to the required gelation rate, and a large amount of encapsulated water gel can be easily produced.
以上の方法で製造したアルミノケイ酸包水ゲル
は低濃度のケイ酸塩およびアルミン酸塩で製造さ
れ蓄熱材料として用いることができるので経済的
に廉価である。 The aluminosilicate hydrogel produced by the above method is economically inexpensive because it is produced with low concentrations of silicate and aluminate and can be used as a heat storage material.
アルミノケイ酸包水ゲルは中性であるからポン
ドから漏水しても全く無害である。包水ゲルは大
量の水を抱え込むため、水の対流を防止すること
ができ、そのため放熱が抑制され、熱が効果的に
蓄えられる。また熱量の目安である比熱は少量の
ケイ酸塩とアルミン酸塩を含有する希薄な溶液で
あるから、水の比熱とほとんど変らず、それに比
較して、塩類水ポンドは比熱の小さい塩類を多量
に使用するため比熱が小さくなり、同温度、同質
量の熱量ならば包水ゲルポンドの方がはるかに多
量の熱量が蓄積していることになる。以上の諸点
は本発明の最も有利な特徴とするところである。 Since aluminosilicate hydrogel is neutral, it is completely harmless even if water leaks from the pond. Because the hydrogel contains a large amount of water, it can prevent water convection, thereby suppressing heat radiation and effectively storing heat. In addition, the specific heat, which is a measure of calorific value, is almost the same as water because it is a dilute solution containing a small amount of silicate and aluminate. Because it is used for water, its specific heat is small, and if the same temperature and mass are used, the hydrogel pond will accumulate a much larger amount of heat. The above points are the most advantageous features of the present invention.
次に本発明を実施例によ詳細に説明するが、本
発明はその要旨をこえない限り以下の実施例に限
定されるものではない。 Next, the present invention will be explained in detail with reference to examples, but the present invention is not limited to the following examples unless it exceeds the gist thereof.
実施例 1
25gの粉末ケイ酸ナトリウムを955mlの水に溶
解したのち、2.5gのアルミン酸ナトリウムを添加
し均一に溶解したのち、5.0gの硫酸を20mlの水に
溶解した溶液を先のケイ酸ナトリウム―アルミン
酸ナトリウム溶液に撹拌しながら滴下し、水素イ
オン濃度が6.8になるように中和した。中和した
ケイ酸ナトリウム―アルミン酸ナトリウム溶液を
1の魔法瓶(内径90mm、深さ230mm)に750ml注
ぎ、約20分後に溶液がゲル化し始め、2時間後に
静かに250mlの水を注入して、ゲル相と水相で1
とした。一方同じ1の魔法瓶に25%の塩化ナ
トリウムを750ml注ぎ、静かに250mlの水を注いで
1とした。Example 1 After dissolving 25g of powdered sodium silicate in 955ml of water, 2.5g of sodium aluminate was added and dissolved uniformly, and a solution of 5.0g of sulfuric acid dissolved in 20ml of water was added to the silicic acid. It was added dropwise to a sodium-sodium aluminate solution with stirring to neutralize the hydrogen ion concentration to 6.8. Pour 750ml of the neutralized sodium silicate-sodium aluminate solution into a thermos flask (inner diameter 90mm, depth 230mm), the solution will begin to gel after about 20 minutes, and after 2 hours, gently pour in 250ml of water. 1 in gel phase and water phase
And so. On the other hand, pour 750 ml of 25% sodium chloride into the same thermos flask, and then gently pour 250 ml of water to make 1.
500Wのタングステン電球の真下に魔法瓶を2
個並べて設置した。電球と魔法瓶の間隔は魔法瓶
の開口部から電球ガラス表面まで300mmで、日射
計による光量は0.804cal・cm-2・mm-1であつた。
温度の測定は各々の魔法瓶の開口部から190mmの
ところに熱電対を設置し、記録計を用いて行なつ
た。光の照射は電球を6時間点灯し、18時間消灯
を反復することによつて太陽の日射とほぼ同じよ
うにした。この点滅行程を長期に経つて測定した
ところ、温度の上昇経過は包水ゲルと食塩を比較
すると包水ゲルの方が常に食塩より高い温度で保
たれた。すなわち6時間点灯した直後の最高温度
と消灯したのち18時間経過した直後の最低温度を
比較すると、包水ゲルの方が食塩よりも高い温度
であつた。約4日間経過した82時間後の最低温度
は包水ゲルの方が4.7℃も高く、また92時間後の
最高温度は包水ゲルの方が8.0℃も高い値が得ら
れた。 Place two thermos bottles directly under the 500W tungsten light bulb.
I installed them side by side. The distance between the bulb and the thermos was 300 mm from the opening of the thermos to the bulb glass surface, and the amount of light measured by the pyranometer was 0.804 cal cm -2 mm -1 .
The temperature was measured using a thermocouple placed 190 mm from the opening of each thermos flask and a recorder. The light irradiation was made to be similar to the solar radiation by repeatedly turning on a light bulb for 6 hours and turning it off for 18 hours. When we measured this blinking process over a long period of time, we found that when we compared the temperature rise of the hydrogel and the salt, the hydrogel was always maintained at a higher temperature than the salt. That is, when comparing the highest temperature immediately after 6 hours of lighting and the lowest temperature immediately after 18 hours had passed after the lights were turned off, the water encapsulation gel had a higher temperature than the salt. The lowest temperature after 82 hours, which was about 4 days, was 4.7°C higher for the water-encapsulant gel, and the highest temperature after 92 hours was 8.0°C higher for the water-enclosed gel.
Claims (1)
酸またはイオン交換樹脂で中和することによつて
得られる反応生成物であるアルミノケイ酸塩包水
ゲルを用いることを特徴とするソーラポンド。 2 包水ゲルが生成するケイ酸塩類としてケイ酸
ナトリウム、ケイ酸カリウム、ケイ酸リチウムな
どのアルカリ塩およびアルカリ土類塩の1種又は
2種以上を使用する特許請求の範囲の第1項記載
の包水ゲルソーラポンド。 3 包水ゲルが生成するアルミン酸塩類としてア
ルミン酸ナトリウム、アルミン酸カリウム、アル
ミン酸リチウムなどのアルカリ塩、アルカリ土類
塩の1種又は2種以上を使用する特許請求の範囲
の第1項記載の包水ゲルソーラポンド。 4 包水ゲルを生成するケイ酸塩類とアルミン酸
塩類との混合溶液の中和剤としての酸は塩酸、硫
酸、硝酸あるいは酢酸、コハク酸、クエン酸、フ
マル酸などの有機酸の1種又は2種以上を使用す
る特許請求の範囲の第1項記載の包水ゲルソーラ
ポンド。 5 包水ゲルを生成するケイ酸塩とアルミン酸塩
類との混合溶液の中和剤としてのイオン交換樹脂
としては弱酸性および強酸性陽イオン交換樹脂の
1種又は2種以上を使用する特許請求の範囲の第
1項記載の包水ゲルソーラポンド。[Claims] 1. The invention is characterized by the use of an aluminosilicate hydrogel, which is a reaction product obtained by neutralizing a mixed solution of silicates and aluminates with an acid or an ion exchange resin. and solar pond. 2. Claim 1 states that one or more of alkali salts and alkaline earth salts such as sodium silicate, potassium silicate, and lithium silicate are used as the silicates from which the hydrogel is produced. Water gel solar pond. 3. Claim 1 states that one or more of alkali salts and alkaline earth salts such as sodium aluminate, potassium aluminate, and lithium aluminate are used as the aluminate salts that form the hydrogel. Water gel solar pond. 4. The acid used as a neutralizing agent for the mixed solution of silicates and aluminates that forms the hydrogel is hydrochloric acid, sulfuric acid, nitric acid, or one of organic acids such as acetic acid, succinic acid, citric acid, fumaric acid, etc. The water-encased gel solar pond according to claim 1, in which two or more types are used. 5. A patent claim that uses one or more of weakly acidic and strongly acidic cation exchange resins as an ion exchange resin as a neutralizing agent for a mixed solution of silicates and aluminates that produce encapsulated water gel. The hydrogel solar pond according to item 1 in the scope of .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58090995A JPS59215381A (en) | 1983-05-24 | 1983-05-24 | Solar pond in gel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58090995A JPS59215381A (en) | 1983-05-24 | 1983-05-24 | Solar pond in gel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59215381A JPS59215381A (en) | 1984-12-05 |
| JPS6340456B2 true JPS6340456B2 (en) | 1988-08-11 |
Family
ID=14014083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58090995A Granted JPS59215381A (en) | 1983-05-24 | 1983-05-24 | Solar pond in gel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59215381A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104249065B (en) * | 2013-06-26 | 2016-12-28 | 浙江昱辉阳光能源有限公司 | A kind of cleaning method of silicon material waste gas absorption tower |
-
1983
- 1983-05-24 JP JP58090995A patent/JPS59215381A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59215381A (en) | 1984-12-05 |
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