JPS6342958B2 - - Google Patents
Info
- Publication number
- JPS6342958B2 JPS6342958B2 JP58079720A JP7972083A JPS6342958B2 JP S6342958 B2 JPS6342958 B2 JP S6342958B2 JP 58079720 A JP58079720 A JP 58079720A JP 7972083 A JP7972083 A JP 7972083A JP S6342958 B2 JPS6342958 B2 JP S6342958B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- hydrogel
- water
- salts
- solar pond
- 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
- 150000003839 salts Chemical class 0.000 claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 239000000017 hydrogel Substances 0.000 claims description 21
- 239000000499 gel Substances 0.000 claims description 13
- 229920000620 organic polymer Polymers 0.000 claims description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 7
- 230000003472 neutralizing effect Effects 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229920000856 Amylose Polymers 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- 150000004676 glycans Chemical class 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 2
- 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
- 229920002125 Sokalan® Polymers 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 2
- 235000010977 hydroxypropyl cellulose Nutrition 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
- 239000001923 methylcellulose Substances 0.000 claims description 2
- 235000010981 methylcellulose Nutrition 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 239000004584 polyacrylic acid Substances 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 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
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims 3
- 150000007524 organic acids Chemical class 0.000 claims 2
- 235000005985 organic acids Nutrition 0.000 claims 2
- PGYZAKRTYUHXRA-UHFFFAOYSA-N 2,10-dinitro-12h-[1,4]benzothiazino[3,2-b]phenothiazin-3-one Chemical compound S1C2=CC(=O)C([N+]([O-])=O)=CC2=NC2=C1C=C1SC3=CC=C([N+](=O)[O-])C=C3NC1=C2 PGYZAKRTYUHXRA-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical class [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 235000012709 brilliant black BN Nutrition 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 229910003460 diamond Inorganic materials 0.000 claims 1
- 239000010432 diamond Substances 0.000 claims 1
- 238000005538 encapsulation Methods 0.000 claims 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims 1
- 229910017053 inorganic salt Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 239000011259 mixed solution Substances 0.000 claims 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical class Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 claims 1
- 235000002639 sodium chloride Nutrition 0.000 description 32
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 10
- 238000005338 heat storage Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000002952 polymeric resin Substances 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 239000011232 storage material Substances 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 7
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 6
- 239000012266 salt solution Substances 0.000 description 5
- 238000001879 gelation Methods 0.000 description 4
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 239000013505 freshwater Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 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 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229940009827 aluminum acetate Drugs 0.000 description 1
- 238000009360 aquaculture Methods 0.000 description 1
- 244000144974 aquaculture Species 0.000 description 1
- 230000004397 blinking Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- FNAQSUUGMSOBHW-UHFFFAOYSA-H calcium citrate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FNAQSUUGMSOBHW-UHFFFAOYSA-H 0.000 description 1
- 239000001354 calcium citrate Substances 0.000 description 1
- 229960004256 calcium citrate Drugs 0.000 description 1
- GUPPESBEIQALOS-UHFFFAOYSA-L calcium tartrate Chemical compound [Ca+2].[O-]C(=O)C(O)C(O)C([O-])=O GUPPESBEIQALOS-UHFFFAOYSA-L 0.000 description 1
- 239000001427 calcium tartrate Substances 0.000 description 1
- 235000011035 calcium tartrate Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000004337 magnesium citrate Substances 0.000 description 1
- 229960005336 magnesium citrate Drugs 0.000 description 1
- 235000002538 magnesium citrate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229940095060 magnesium tartrate Drugs 0.000 description 1
- MUZDLCBWNVUYIR-ZVGUSBNCSA-L magnesium;(2r,3r)-2,3-dihydroxybutanedioate Chemical compound [Mg+2].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O MUZDLCBWNVUYIR-ZVGUSBNCSA-L 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- PLSARIKBYIPYPF-UHFFFAOYSA-H trimagnesium dicitrate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O PLSARIKBYIPYPF-UHFFFAOYSA-H 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
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/40—Solar thermal energy, e.g. solar towers
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方法は
塩類溶液を用いて濃度勾配を作り対流を防いで断
熱効果を上げて放熱を抑制することである。この
濃度勾配を形成するには、塩の種類や濃度によつ
て異なるが濃厚塩溶液に真水を注入すればよい。
この濃度勾配に応じて密度勾配が形成され、この
密度勾配により、温度差による密度差の発生を防
止し、さらに浮力による対流の発生をも防止する
ことができる。対流が防止されれば放熱が抑制さ
れて長期の蓄熱が可能となる。 The conventional method of collecting and storing heat in a solar pond is to use a salt solution to create a concentration gradient to prevent convection, increase the heat insulation effect, and suppress heat radiation. To form this concentration gradient, fresh water may be injected into the concentrated salt solution, depending on the type and concentration of the salt.
A density gradient is formed in accordance with this concentration gradient, and this density gradient prevents the occurrence of a density difference due to a temperature difference, and also prevents 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のよ
うな欠点がある。 However, salt water solar ponds have the following drawbacks.
第一に濃塩類溶液に真水を流して、濃度勾配を
強制的に形成する方法であるため、常時上層部に
真水を流す必要があるので保守管理に経費と手数
が必要である。第二にこの方法は塩類水勾配の形
成を行つて蓄熱を開始するまでに数カ月の期間を
要する。第三に漏水による塩害があるので魚の孵
化や養殖などの塩害が致命的なものには使用でき
ない。第四に塩類水は20%以上にしなければなら
ないため大量の塩類が必要であることは経済的に
有利でない。第五に塩類の内、硼酸のソーダは長
期間使用すると塩が沈降し底部が白くなる。その
他塩類は透明であるが、食塩の価格と比べて高
く、食塩以外は経済的に使えない。第六に蓄熱量
は比熱と温度および質量の積によつて現わされる
が、水の比熱が一番大きい、それ故同温度で同質
量の熱量は水が一番大きいことになる。一般に塩
類は比熱が小さく、塩類溶液の比熱は溶液の比重
が大きくななるにしたがつて小さくなるから同温
度で同質量の高濃度塩類溶液の熱量は少なくな
る。それ故濃厚塩水ソーラポンドは効率が悪いと
いえる。第七に藻、泥や砂など混入した場合には
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。 First, since it is a method of forcing fresh water to flow through a concentrated salt solution to form a concentration gradient, it is necessary to constantly flow fresh water into the upper layer, which requires maintenance and management costs and effort. Second, this method requires several months to build up the saline gradient and begin heat storage. Third, it causes salt damage due to water leakage, so it cannot be used for fish hatching or aquaculture where salt damage is fatal. Fourth, since the saline water content must be at least 20%, the need for a large amount of salt is not economically advantageous. Fifth, among salts, if boric acid soda is used for a long period of time, the salt will settle and the bottom will turn white. Although other salts are transparent, they are expensive compared to table salt, and anything other than table salt cannot be used economically. Sixth, the amount of heat stored is expressed as the product of specific heat, temperature, and mass, and the specific heat of water is the largest, so water has the largest amount of heat for the same mass at the same temperature. Generally, salts have a small specific heat, and the specific heat of a salt solution decreases as the specific gravity of the solution increases, so the amount of heat of a highly concentrated salt solution of the same mass at the same temperature decreases. Therefore, it can be said that concentrated salt water solar ponds are inefficient. Seventh, 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 takes into account the above-mentioned drawbacks, and as a result of intensive research into a heat storage material for solar ponds that can collect and store a large amount of heat, it is possible to achieve the objective 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水溶液有機高分子を溶解
した水溶液を酸、塩化物など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、蓄熱効果を従来の塩類
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。 In the present invention, an aqueous solution of an aqueous organic polymer dissolved in a silicate is neutralized with an acid, chloride, etc. to generate a gel-like substance, and this is used as a heat storage material for a solar pond. The present invention provides a heat storage material that is significantly improved over water solar ponds.
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)でもよい。また水溶性有
機高分子樹脂としてはカルボキシメチルセルロー
ス、ヒドロキシプロピルセルロース、ヒドロキシ
メチルセルロース、メチルセルロースなどのセル
ロース系、アミロースなどの多糖類誘導体、ポリ
アクリル酸ヒドロキシエチル、ポリアクリル酸お
よびその塩、ポリメタクリル酸およびその塩、ポ
リビニルピロリドン、ポリビニルアルコールのい
ずれでもケイ酸塩とよく混合し均一な包水ゲルが
生成する。中和剤としての塩類は塩化マグネシウ
ム、塩化カルシウム、塩化アルミニウムなどの塩
化物、または硝酸マグネシウム、硝酸カルシウ
ム、硝酸アルミニウムなどの硝酸塩、または硫酸
マグネシウム、硫酸カルシウム、硫酸アルミニウ
ムなどの硫酸塩、または酢酸マグネシウム、酢酸
カルシウム、酢酸アルミニウムなどの酢酸塩およ
び他の酸類、例えば有機酸塩であるクエン酸マグ
ネシウムクエン酸カルシウム、酒石酸マグネシウ
ム、酒石酸カルシウムなどの有機塩類で、上記い
ずれの塩類でもゲルが生成する。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。 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 the form of a powder or a concentrated solution (candy-like). Water-soluble organic polymer resins include cellulose-based resins such as carboxymethylcellulose, hydroxypropylcellulose, hydroxymethylcellulose, and methylcellulose, polysaccharide derivatives such as amylose, hydroxyethyl polyacrylate, polyacrylic acid and its salts, polymethacrylic acid and its salts, etc. Salt, polyvinylpyrrolidone, and polyvinyl alcohol all mix well with silicate to form a uniform hydrogel. Salts as neutralizing agents include chlorides such as magnesium chloride, calcium chloride, and aluminum chloride, or nitrates such as magnesium nitrate, calcium nitrate, and aluminum nitrate, or sulfates such as magnesium sulfate, calcium sulfate, and aluminum sulfate, or magnesium acetate. , acetates such as calcium acetate, aluminum acetate, and other acids, such as organic salts such as magnesium citrate, calcium citrate, magnesium tartrate, and calcium tartrate. Gels are formed with any of the above salts. Acids used as neutralizing agents include hydrochloric acid, sulfuric acid, nitric acid, acetic acid, succinic acid, citric acid, and fumaric acid.
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を溶解し
たのち、水溶性有機高分子樹脂を加えて完全に溶
解したのち、酸や塩で中和すれば、水を多量に含
んだ、いわゆる包水ゲルが生成するが、ケイ酸塩
単独の包水ゲルより水溶性有機高分子樹脂を添加
した場合の方がケイ酸塩が少なくても包水ゲルが
生成し、なおかつ透明度がよくなり、光の吸収効
率が上昇する。経済的にはゲルが多量の水を含
み、なおかつ流動性が起らないようなケイ酸塩お
よび水溶性有機高分子樹脂の濃度が望ましい。通
常用いられるケイ酸塩濃度としては0.1%から10
%が、また水溶性有機高分子樹脂の濃度としては
0.1%から5%が最適である。 The reaction conditions for gel production and the optimal conditions for use as a heat storage material are as follows: After dissolving the silicate, a water-soluble organic polymer resin is added to completely dissolve the gel, and then the gel is neutralized with acid or salt. For example, a so-called hydrogel containing a large amount of water is formed, but a hydrogel containing a water-soluble organic polymer resin is better than a hydrogel containing only silicate even if the silicate content is small. is generated, the transparency is improved, and the light absorption efficiency is increased. Economically, it is desirable to have a concentration of the silicate and water-soluble organic polymer resin such that the gel contains a large amount of water and does not cause fluidity. The commonly used silicate concentrations range from 0.1% to 10
%, and the concentration of water-soluble organic polymer resin
0.1% to 5% is optimal.
中和する条件としては、酸や塩などの種類によ
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
度によつて決まるが、たとえば20℃で25%のケイ
酸ナトリウムと2%のポリビニルアルコールを溶
解した溶液を50%の硫酸で水素イオン濃度7.0に
中和したとき、1時間でゲル化が始まり、2〜3
時間で完結する。また塩類である塩化アルミニウ
ムの場合にはケイ酸ナトリウム―ポリビニルアル
コール水溶液に塩化アルミニウム水溶液を添加し
た時点で直ちにゲル化が起る。ゲル化に使用する
酸、塩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。さらに墨や黒色の染料を用いれば一
層光吸収が上がる。 Although the concentration and amount of neutralizing conditions vary depending on the type of acid or salt, 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. For example, a solution of 25% sodium silicate and 2% polyvinyl alcohol at 20°C is mixed with 50% sulfuric acid at a hydrogen ion concentration of 7.0. When neutralized to
It will be completed in time. In the case of aluminum chloride, which is a salt, gelation occurs immediately upon adding the aluminum chloride aqueous solution to the sodium silicate-polyvinyl alcohol aqueous solution. The acid and salt used for gelation can be selected according to the required gelation rate, and a large amount of encapsulated water gel can be easily produced. Furthermore, using ink or black dye will further increase light absorption.
以上の方法で製造した包水ゲルは低濃度のケイ
酸塩および水溶性有機高分子樹脂で蓄熱材料とし
て用いることができるので経済的に廉価である。 The hydrogel produced by the above method is economically inexpensive because it can be used as a heat storage material with a low concentration of silicate and water-soluble organic polymer resin.
ケイ酸塩は粉末あるいはアメ状であるし、水溶
性有機高分子樹脂もまた粉末状であるから僻地へ
の運般は容易であるし、生成した包水ゲルは中性
であるからポンドから漏水しても全く無害であ
る。包水ゲルは少量のケイ酸塩と水溶性有機高分
子樹脂によつて大量の水を抱え込むため、水の対
流を防止し、放熱を抑制するため、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
ケイ酸塩および比熱の小さい有機高分子樹脂を含
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。 Silicates are powder or candy-like, and water-soluble organic polymer resins are also powder, so they can be easily transported to remote areas, and the water gel produced is neutral, so there is no possibility of water leaking from the pond. However, it is completely harmless. Hydrogel contains a large amount of water with a small amount of silicate and a water-soluble organic polymer resin, which prevents water convection and suppresses heat radiation, so heat can be stored effectively. In addition, the specific heat, which is a measure of the amount of heat, is almost the same as that of water because it is a dilute solution containing a small amount of silicate and an organic polymer resin with a small specific heat.In comparison, salt water has a small specific heat. Because a large amount of salt is used, the 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り詳細に説明するが、
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 by examples.
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、2gのポリビニルアルコールを添加
し均一に溶解したのち、4.5g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―ポリビ
ニルアルコール溶液に撹拌しながら滴下し、水素
イオン濃度を7.0になるように中和した。中和し
たケイ酸ソーダ―ポリビニルアルコール溶液を1
の魔法瓶(内径90mm、深さ230mm)に750mlを注
ぎ、約1時間後に溶液がゲル化し始め、3時間後
に静かに250mlの水を注入し、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, 2g of polyvinyl alcohol was added and dissolved uniformly, and a solution of 4.5g of sulfuric acid dissolved in 20ml of water was added to the sodium silicate solution. It was added dropwise to a polyvinyl alcohol solution with stirring to neutralize the hydrogen ion concentration to 7.0. 1 neutralized sodium silicate-polyvinyl alcohol solution
Pour 750ml into a thermos flask (inner diameter 90mm, depth 230mm), the solution will start to gel after about 1 hour, and after 3 hours, gently pour in 250ml of water, and the gel phase and water phase will be combined.
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・min-1である。
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常に高い
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5.2℃も高く、また92時間
後の最高温度は包水ゲルの方が8.5℃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 is 300 mm from the opening of the thermos to the bulb glass surface, and the amount of light measured by the pyranometer is 0.804 cal cm -2 min -1 .
The temperature was measured using a thermocouple placed 190 mm from the opening of each thermos flask and a recorder. Light irradiation was achieved by repeatedly turning on a light bulb for 6 hours and then turning it off for 18 hours to make it almost the same as the solar radiation. 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 always maintained a higher temperature than the salt. In other words, 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 temperature of the encapsulated water gel was always higher than that of common salt. The minimum temperature after 82 hours, which is about 4 days, was 5.2°C higher for the hydrogel, and the maximum temperature after 92 hours was 8.5°C higher for the hydrogel.
Claims (1)
たはそれに染料を添加した水溶液を酸、塩類で中
和することによつて得られる反応生成物である包
水ゲルを用いることを特徴とする包水ゲルソーラ
ポンド。 2 包水ゲルが生成する無機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 包水ゲル中に含有する水溶性有機高分子とし
てポリビニルアルコール、カルボキシメチルセル
ロース、ヒドロキシプロピルセルロース、ヒドロ
キシエチルセルロース、メチルセルロースなどの
セルロース系水溶性樹脂、アミロースなどの多糖
類誘導体、ポリアクリル酸ヒドロキシエチル、ポ
リメタアクリル酸およびその塩、ポリアクリル酸
およびその塩、ポリビニルピロリドンの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無機塩類の中和剤として
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で、その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無機塩類の中和剤として
の塩類はマグネシウム、カルシウム、マンガン、
アルミニウム、第一銅、第二銅、第一鉄、第二
鉄、ニツケルの塩化物、硝酸または硫酸の酸金属
塩および酢酸、フマル酸、クエン酸、コハク酸な
どの有機酸の酸金属塩の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。 6 包水ゲル中に含有する染料は墨、サルフアブ
ラツク、ダイアモンドブラツク、ナフトールブラ
ツクなど黒色を発色する染料の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。[Scope of Claims] 1. Uses a hydrogel, which is a reaction product obtained by neutralizing a mixed solution of an inorganic salt and a water-soluble organic polymer or an aqueous solution to which a dye is added, with an acid or a salt. A hydrogel solar pond characterized by: 2. One or two of alkali salts and alkaline earth salts such as sodium silicate, potassium silicate, and lithium silicate as the inorganic salts that form the hydrogel.
1. The water-enriched gel solar pond according to claim 1, wherein more than one species is used. 3 Water-soluble organic polymers contained in the hydrogel include polyvinyl alcohol, cellulose-based water-soluble resins such as carboxymethyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose, and methyl cellulose, polysaccharide derivatives such as amylose, polyhydroxyethyl acrylate, and polysaccharide derivatives such as amylose. The water-encapsulated gel solar pond according to claim 1, which uses one or more of methacrylic acid and its salts, polyacrylic acid and its salts, and polyvinylpyrrolidone. 4 Acids that can be used as neutralizing agents for inorganic salts that produce hydrogel include hydrochloric acid, sulfuric acid, nitric acid, or organic acids such as acetic acid, succinic acid, citric acid, and fumaric acid.
The first claim using a species or two or more species
Water encapsulation gel solar pond described in section. 5 Salts used as neutralizing agents for inorganic salts that produce hydrogel include magnesium, calcium, manganese,
Acid metal salts of aluminum, cuprous, cupric, ferrous, ferric, nickel chlorides, nitric or sulfuric acids and organic acids such as acetic acid, fumaric acid, citric acid, succinic acid, etc. The hydrogel solar pond according to claim 1, in which one or more types are used. 6. The hydrogel solar pond according to claim 1, wherein the dye contained in the hydrogel is one or more of black coloring dyes such as ink, sulfur black, diamond black, and naphthol black. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58079720A JPS59204681A (en) | 1983-05-06 | 1983-05-06 | Solar gel pond |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58079720A JPS59204681A (en) | 1983-05-06 | 1983-05-06 | Solar gel pond |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59204681A JPS59204681A (en) | 1984-11-20 |
| JPS6342958B2 true JPS6342958B2 (en) | 1988-08-26 |
Family
ID=13698031
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58079720A Granted JPS59204681A (en) | 1983-05-06 | 1983-05-06 | Solar gel pond |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59204681A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0241723U (en) * | 1988-09-14 | 1990-03-22 |
-
1983
- 1983-05-06 JP JP58079720A patent/JPS59204681A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0241723U (en) * | 1988-09-14 | 1990-03-22 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59204681A (en) | 1984-11-20 |
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