Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
  • C09K5/02—Materials undergoing a change of physical state when used
  • C09K5/06—Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
  • C09K5/063—Materials absorbing or liberating heat during crystallisation; Heat storage materials

Definitions

• the present invention is concerned with thermal energy storage materials and heat-exchange devices containing such materials.
• Thermal energy storage materials may store thermal energy as specific heat and/or as latent heat. It is often desirable to use materials which store thermal energy as latent heat, since this enables the volume occupied by the storage material to be minimised. This is advantageous, for example, in materials operating in the temperature range 10°C to 100°C for the storage of solar energy or of heat extracted during refrigeration.
• a number of hydrated inorganic salts are known which undergo transition to the anhydrous or a less hydrated form at a characteristic temperature on heating and revert to the more hydrated form on cooling.
• a potential drawback in the use of many of these hydrated salts is incongruency of the phase transition, that is, the transformation of the low-temperature solid phase to a two-phase condition where a solid and liquid coexist.
• the difference in densities of the two phases causes segregation thereof, which limits their ability to recombine and form the low-temperature single solid phase. Consequently the amount of heat recoverable on cooling is reduced.
• Thermal energy storage materials have been proposed in which the hydrated inorganic salt is thickened by an organic thickening agent, for example, cellulosic polymers, starch, aliginates or an inorganic thickening agent, such as a clay (as disclosed in U.S. Patent 3 986 969).
• organic thickening agents are natural polymers (or derivatives thereof) and are therefore unstable to hydrolysis and bacterial and enzyme action, which considerably shortens the life of the material.
• the above-mentioned inorganic thickening agents are more stable, but it appears that thermal energy storage materials containing such thickening agents can only be used in very shallow depths (for example, about one inch) and must therefore be disposed horizontally.
• thermo energy storage material in which a hydrated inorganic salt having a transition temperature to the anhydrous or a less hydrated form in the range 10° to 100°C is dispersed and suspended in a hydrogel formed from a water-soluble synthetic polymer having pendant carboxylic or sulphonic acid groups cross-linked with cations of a polyvalent metal.
• this material is that the hydrated inorganic salt is immobilised in close proximity in small volumes throughout the gel. This minimises any segregation which could arise, after fusion of the hydrate phase, by any solid sinking to the bottom of the mixture.
• the material according to the invention in flat horizontal trays; the material can be arranged in vertical columns of substantial height (for example 50 cm. to one metre).
• a further advantage of the material according to the invention is that the cross-linked hydrogel can be prepared in situ by reaction between the respective water-soluble polymer or an alkali metal or ammonium salt thereof and a water-soluble salt of the polyvalent metal.
• Suitable polyvalent metals include, for example, chromium, iron, tin, magnesium and aluminium. Aluminium and magnesium are preferred in view of the ready availability of water-soluble salts thereof. Suitable water-soluble salts of the above metals include, for example, chlorides, nitrates or sulphates, of which aluminium sulphate and magnesium sulphate are preferred.
• the polyvalent metal is preferably present in an amount sufficient to react with all the acid groups in the polymer to form ionic cross-links. The actual amount necessary to achieve complete reaction depends on factors such as the valency of the metal, the proportion of acid groups in the polymer and the amount of polymer in the material. Typical amounts of polyvalent metal are 0.5 to 5% (expressed as the weight of water-soluble salt, based on the weight of the storage material).
• the water-soluble polymer preferably has a backbone containing units of acrylic acid or methacrylic acid, for example, a homopolymer or copolymer or acrylic acid or methacrylic acid, partially hydrolysed polyacrylamide or polymethacrylamide, or an alkali metal or ammonium salt thereof.
• the polymer preferably contains 5 to 50% (for example 10 to 40%) carboxylic groups, the percentages being based on the number of repeating units in the polymer backbone.
• the molecular weight of the polymer may vary over a wide range. For some applications it may be advantageous to use polymers of relatively low molecular weight (for example, 100,000 to 500,000), while for other applications, higher molecular weights (for example 1 million to 8 million) may be preferred.
• the water-soluble polymer is preferably present in the thermal energy storage material in a relatively minor amount, such as from 0.5 to 10% (for example, about 5%), based on the weight of the material.
• Suitable hydrated inorganic salts for use in the material according to the present invention include, for example, calcium chloride hexahydrate (the fusion point of which is 29°C); sodium sulphate decahydrate (the fusion point of which is 32°C); disodium hydrogen phosphate dodecahydrate (the fusion point of which is 35.5°C); sodium thiosulphate pentahydrate (the fusion point of which is 50°C); sodium acetate trihydrate (the fusion point of which is 58°C); barium hydroxide octahydrate (the fusion point of which is 75°C) and zinc nitrate hexahydrate (the fusion point of which is 35°C).
• the hydrated salt preferably has a fusion point in the range 20° to 90°C and is preferably non-toxic, noncorrosive and readily available at low cost.
• Preferred hydrated salts meeting some or all of the above requirements are sodium sulphate decahydrate, disodium hydrogen phosphate dodecahydrate, sodium thiosulphate pentahydrate and sodium carbonate decahydrate.
• the material may be nucleated, for example, by a heat transfer method as disclosed in U.S. Patent 2 677 243, by careful control of the proportions of the ingredients of the composition, or by addition of an insoluble nucleating agent.
• a preferred nucleating agent for sodium sulphate decahydrate is borax, as proposed in U.S. Patent 2 677 664.
• this agent like the inorganic salt, is dispersed and suspended in the hydrogel and effectively immobilized therein. This wide dispersion of immobilized nucleating agent ensures efficient nucleation of the hydrate phase during cooling cycles, thereby inhibiting supercooling.
• the thermal energy storage material according to the invention preferably contains the hydrated salt in an amount of from 66% to 95% by weight and, optionally, a nucleating agent in an amount of from 1 to 10%, based on the weight of the hydrated salt.
• Substantially all the balance of the thermal energy storage material according to the invention is preferably water and, optionally, an organic liquid which is miscible with water.
• a particularly preferred such organic liquid is a lower aliphatic alcohol, such as ethanol (for example, when the hydrated salt is sodium sulphate decahydrate).
• the water is preferably present in an amount sufficient to hydrate all the anhydrous inorganic salt, and is preferably present in a small excess.
• the material may contain water in an amount of, for example, from 25 to 75% by weight.
• a water-miscible organic liquid is included, it is preferably present in a relatively minor amount, compared with water, for example, from 5 to 25%, based on the weight of water.
• the material according to the invention is preferably used in a method of heat exchange in which the material is first heated to a temperature above the transition temperature of the hydrated salt, and the heat is extracted from the material by passing a fluid at a temperature below the above mentioned transition temperature in heat-exchange relationship therewith.
• the alternate heating and cooling of the material can be repeated for many cycles.
• the present invention also comprises a heat-exchange device, which comprises a tank containing the thermal energy storage material according to the invention and means for supplying a cooling fluid in heat-exchange relationship with the thermal energy storage material.
• a sample of the solid was sealed in a square section tube measuring 5 cm. x 5 cm. x 50 cm. long, made of inert plastics. The ends of the tube were sealed by cast epoxy resin plugs.
• the tube was disposed vertically and alternately heated to about 60°C (the heating time being about one hour) and cooled to about 20°C by heat-exchangeing with water circulating outside the tube (the cooling time being three to four hours). Reproducible thermal arrests were obtained for more than 500 cycles of heating and cooling.
• Example 1 was repeated, except that the aluminium sulphate was replaced by the same amount of MgS0 4 .7H 2 0.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Combustion & Propulsion (AREA)
• Thermal Sciences (AREA)
• Physics & Mathematics (AREA)
• Organic Chemistry (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Processes Of Treating Macromolecular Substances (AREA)
• Sorption Type Refrigeration Machines (AREA)
• Thermotherapy And Cooling Therapy Devices (AREA)
• Physical Or Chemical Processes And Apparatus (AREA)

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Publications (2)

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• 1977
  • 1977-06-10 GB GB24279/77A patent/GB1584559A/en not_active Expired
• 1978
  • 1978-06-06 NO NO781971A patent/NO147797C/no unknown
  • 1978-06-06 IE IE1152/78A patent/IE47083B1/en unknown
  • 1978-06-06 IN IN417/DEL/78A patent/IN148032B/en unknown
  • 1978-06-07 US US05/913,351 patent/US4209413A/en not_active Expired - Lifetime
  • 1978-06-07 AU AU36895/78A patent/AU513058B2/en not_active Expired
  • 1978-06-07 ZA ZA00783256A patent/ZA783256B/xx unknown
  • 1978-06-08 AR AR272497A patent/AR217299A1/es active
  • 1978-06-08 PT PT68155A patent/PT68155A/pt unknown
  • 1978-06-08 FI FI781830A patent/FI64808C/fi not_active IP Right Cessation
  • 1978-06-09 NZ NZ187511A patent/NZ187511A/xx unknown
  • 1978-06-09 IT IT24388/78A patent/IT1112264B/it active
  • 1978-06-09 BR BR787803722A patent/BR7803722A/pt unknown
  • 1978-06-09 MX MX173765A patent/MX147710A/es unknown
  • 1978-06-09 DE DE7878300030T patent/DE2860041D1/de not_active Expired
  • 1978-06-09 EP EP78300030A patent/EP0000099B1/en not_active Expired
  • 1978-06-09 DK DK259778A patent/DK259778A/da not_active Application Discontinuation
  • 1978-06-09 AT AT0423478A patent/AT379407B/de not_active IP Right Cessation
  • 1978-06-09 ES ES470660A patent/ES470660A1/es not_active Expired
  • 1978-06-09 GR GR56482A patent/GR64536B/el unknown
  • 1978-06-10 JP JP7028078A patent/JPS5416387A/ja active Granted
  • 1978-06-12 CA CA305,211A patent/CA1103454A/en not_active Expired
  • 1978-06-16 IL IL54932A patent/IL54932A/xx unknown

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