CN109504352A - 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof - Google Patents

8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof Download PDF

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Publication number
CN109504352A
CN109504352A CN201811635401.9A CN201811635401A CN109504352A CN 109504352 A CN109504352 A CN 109504352A CN 201811635401 A CN201811635401 A CN 201811635401A CN 109504352 A CN109504352 A CN 109504352A
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Prior art keywords
parts
preparation
phase change
cool storage
storage materials
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CN201811635401.9A
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Chinese (zh)
Inventor
孟帅
贾维
杜海兵
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Beijing Hua Yuan Energy Technology Co Ltd
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Beijing Hua Yuan Energy Technology Co Ltd
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Priority to CN201811635401.9A priority Critical patent/CN109504352A/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-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
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/06Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
    • C09K5/066Cooling mixtures; De-icing compositions
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/14Thermal energy storage

Abstract

The invention discloses a kind of 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials and preparation method thereof, comprising mass fraction be 50 ~ 60 parts sal glauberi as material of main part;8 ~ 15 parts of potassium chloride, 3 ~ 5 parts of ammonium sulfate, 2 ~ 5 parts of boric acid, 1 ~ 3 part of borax is as nucleating agent;2 ~ 4 parts of attapulgite clays, 2 ~ 4 lithium magnesium silicates, as thickener;1 ~ 5 part of hydrophily aeroge is as suspending agent and 10 ~ 25 parts of deionized water.Phase transformation enthalpy reaches 200 ~ 220kJ/kg, and degree of supercooling is small, and energy storage density is big, and without mutually separating, stability is high, and be widely used market in cold chain, chilling air conditioning system and process industrial.

Description

8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof
Technical field
The present invention relates to energy storage material fields, more specifically to a kind of 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials And preparation method thereof.
Background technique
With China's Energy restructuring, renewable energy ratio is risen year by year, and integrated energy system and service become hair Exhibition trend is coordinated further promote efficiency of energy utilization with the cascade utilization of the energy by multipotency.In this respect, energy storage technology Technical support is provided for the conversion of a variety of clean energy resourcies.Wherein phase change cold-storage material can be applied to Solar use, Heating,Ventilating and Air Conditioning system System and process industrial etc..For phase transition temperature within the scope of 8 ~ 10 DEG C, in combination with water cold storage and ice-storage system, energy conservation drop This, is obviously improved the refrigerating efficiency of refrigeration machine.But compare existing cool storage material, often exist cold storage capacity it is low, layering and not Can crystal counter the problems such as, Chinese patent CN10760182A and CN108251068 China using sodium carboxymethylcellulose as ten water The thickener of sodium sulphate system, it may appear that phase transition temperature hysteresis effect is larger, and corruption is degradable;And Chinese patent The disodium hydrogen phosphate dodecahydrate of CN103059816A patent, sal glauberi, washing soda system system, preparation use poly- third Olefin(e) acid sodium is as thickener.
Summary of the invention
For overcome the deficiencies in the prior art, the purpose of the present invention be directed to a kind of 8 ~ 10 DEG C of composite phase-change materials and its Preparation method, the material have the characteristics that cheap, nontoxic, degree of supercooling is small, energy storage density is high, performance is stable, can be applied to cold chain Transport, the phase change cold-storage system of air-conditioning and process industrial need in 8 ~ 10 DEG C of usage scenario.
To achieve the above objectives, the technical solution adopted by the present invention is that:
8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof, the ten water sulphur for being 50 ~ 60 parts comprising mass fraction Sour sodium is as material of main part;8 ~ 15 parts of potassium chloride, 3 ~ 5 parts of ammonium sulfate, 2 ~ 5 parts of boric acid, 1 ~ 3 part of borax is as nucleation Agent;2 ~ 4 parts of attapulgite clays, 2 ~ 4 lithium magnesium silicates, as thickener;1 ~ 5 part of hydrophily aeroge as suspending agent and 10 ~ 25 parts of deionized water.
Preferably, thickener is mixed in proportion using attapulgite clay and lithium magnesium silicate.
A kind of preparation method of 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials, includes the following steps:
Step 1: anhydrous sodium sulfate, potassium chloride, ammonium sulfate, boric acid, borax are uniformly mixed in proportion, obtain original mixture;
Step 2: original mixture is heated to 65 ~ 70 DEG C of molten conditions in the reaction vessel, is heated while stirring, in proportion Lithium magnesium silicate, attapulgite clay is added, part hydrophily aeroge supplements and deionized water is added, continues to stir 30min after adding, Then lotion is naturally cooled to, uniformly mixed phase-change material is obtained.
Compared with prior art, beneficial effects of the present invention:
(1) thickener is used as using the collaboration system of attapulgite clay and lithium magnesium silicate, decrease phase transition temperature hysteresis with mutually separate Phenomenon, system are more uniform.
(2) phase transition temperature is 8 ~ 10 DEG C, and using inorganic phase-changing material system, raw material are easily obtained, safe and non-toxic, enthalpy model It is trapped among 200 ~ 220kJ/kg, material circulation stability is good, lower phase transition temperature hysteresis, in chilling air conditioning system and process industrial And other need 8 ~ 10 DEG C of temperature occasions to have very big application value.
Detailed description of the invention
Fig. 1 is the cooling curve of various embodiments of the present invention, wherein A is embodiment 1, and B is embodiment 2, and C is embodiment 3.
Specific embodiment
To further illustrate the present invention, illustrate with the following Examples.
Embodiment 1
Step 1: according to the mass fraction of each raw material, weighing 55 parts of sal glauberis, 8 parts of potassium chloride, 5 parts of ammonium sulfate, and 2 parts Boric acid, 2 parts of boraxs uniformly mix, obtain original mixture;
Step 2: original mixture is heated to 65 ~ 70 DEG C of molten conditions in the reaction vessel, is heated while stirring, in proportion 2 parts of lithium magnesium silicates, 3 parts of attapulgite clays are added, 2 parts of hydrophily aeroges supplement and 13 parts of deionized waters are added, continue after adding 30min is stirred, lotion is then naturally cooled to, obtains uniformly mixed phase-change material.8.2 ~ 9.1 DEG C of transition temperature range.
Embodiment 2
Step 1: according to the mass fraction of each raw material, weighing 50 parts of sal glauberis, 10 parts of potassium chloride, 3 parts of ammonium sulfate, and 2 parts Boric acid, 3 parts of boraxs uniformly mix, obtain original mixture;
Step 2: original mixture is heated to 65 ~ 70 DEG C of molten conditions in the reaction vessel, is heated while stirring, in proportion 2 parts of lithium magnesium silicates, 3 parts of attapulgite clays are added, 2 parts of hydrophily aeroges supplement and 21.5 parts of deionized waters are added, add subsequent Continuous stirring 30min, then naturally cools to lotion, obtains uniformly mixed phase-change material.8.4 ~ 9.4 DEG C of transition temperature range.
Embodiment 3
Step 1: according to the mass fraction of each raw material, weighing 60 parts of sal glauberis, 15 parts of potassium chloride, 3 parts of ammonium sulfate, and 3 parts Boric acid, 3 parts of boraxs uniformly mix, obtain original mixture;
Step 2: original mixture is heated to 65 ~ 70 DEG C of molten conditions in the reaction vessel, is heated while stirring, in proportion 2 parts of lithium magnesium silicates, 2 parts of attapulgite clays are added, 2 parts of hydrophily aeroges supplement and 10 parts of deionized waters are added, continue after adding 30min is stirred, lotion is then naturally cooled to, obtains uniformly mixed phase-change material.9.2 ~ 10.5 DEG C of transition temperature range.
Specific embodiments of the present invention are described above.It is to be appreciated that the present invention is not limited to above-mentioned spies Determine embodiment, those skilled in the art can make various deformations or amendments within the scope of the claims, have no effect on this hair Bright substantive content.

Claims (2)

1. 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof, it is characterised in that: comprising mass fraction be 30 ~ 50 parts of anhydrous sodium sulfate is as material of main part;It is 50 ~ 60 parts of sal glauberi as material of main part comprising mass fraction;8~ 15 parts of potassium chloride, 3 ~ 5 parts of ammonium sulfate, 2 ~ 5 parts of boric acid, 1 ~ 3 part of borax is as nucleating agent;2 ~ 4 parts of attapulgite clays, 2 ~ 4 lithium magnesium silicates, as thickener;1 ~ 5 part of hydrophily aeroge is as suspending agent and 10 ~ 25 parts of deionized water.
2. the preparation method of 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind, includes the following steps:
Step 1: anhydrous sodium sulfate, potassium chloride, ammonium sulfate, boric acid, borax are uniformly mixed in proportion, obtain original mixture;
Step 2: original mixture is heated to 65 ~ 70 DEG C of molten conditions in the reaction vessel, is heated while stirring, in proportion Lithium magnesium silicate, attapulgite clay is added, part hydrophily aeroge supplements and deionized water is added, continues to stir 30min after adding, Then lotion is naturally cooled to, uniformly mixed phase-change material is obtained.
CN201811635401.9A 2018-12-29 2018-12-29 8 ~ 10 DEG C of composite phase change energy-storing cool storage materials of one kind and preparation method thereof Withdrawn CN109504352A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113861943A (en) * 2021-10-19 2021-12-31 佛山市顺德区美的洗涤电器制造有限公司 Phase-change material composition, phase-change material, and preparation method and application thereof
CN113861944A (en) * 2021-10-19 2021-12-31 佛山市顺德区美的洗涤电器制造有限公司 Inorganic hydrated salt phase-change material composition, inorganic hydrated salt phase-change material, and preparation method and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105154023A (en) * 2015-09-29 2015-12-16 苏州三拓冷链技术有限公司 Phase change cold-accumulation material and preparation method thereof
CN107189765A (en) * 2017-07-06 2017-09-22 贺迈新能源科技(上海)有限公司 A kind of deepfreeze hydrous salt phase change material and its preparation method and application
CN107418521A (en) * 2017-07-11 2017-12-01 江苏理工学院 A kind of ternary phase-change material for cold storage and preparation method thereof
CN108531136A (en) * 2018-04-08 2018-09-14 曹斌斌 A kind of high efficiency composition phase-change material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105154023A (en) * 2015-09-29 2015-12-16 苏州三拓冷链技术有限公司 Phase change cold-accumulation material and preparation method thereof
CN107189765A (en) * 2017-07-06 2017-09-22 贺迈新能源科技(上海)有限公司 A kind of deepfreeze hydrous salt phase change material and its preparation method and application
CN107418521A (en) * 2017-07-11 2017-12-01 江苏理工学院 A kind of ternary phase-change material for cold storage and preparation method thereof
CN108531136A (en) * 2018-04-08 2018-09-14 曹斌斌 A kind of high efficiency composition phase-change material and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113861943A (en) * 2021-10-19 2021-12-31 佛山市顺德区美的洗涤电器制造有限公司 Phase-change material composition, phase-change material, and preparation method and application thereof
CN113861944A (en) * 2021-10-19 2021-12-31 佛山市顺德区美的洗涤电器制造有限公司 Inorganic hydrated salt phase-change material composition, inorganic hydrated salt phase-change material, and preparation method and application thereof
CN113861944B (en) * 2021-10-19 2023-10-27 佛山市顺德区美的洗涤电器制造有限公司 Inorganic hydrated salt phase-change material composition, inorganic hydrated salt phase-change material, and preparation method and application thereof
CN113861943B (en) * 2021-10-19 2023-11-10 佛山市顺德区美的洗涤电器制造有限公司 Phase change material composition, phase change material, preparation method and application thereof

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