CN112480871A - Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof - Google Patents

Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof Download PDF

Info

Publication number
CN112480871A
CN112480871A CN202011271745.3A CN202011271745A CN112480871A CN 112480871 A CN112480871 A CN 112480871A CN 202011271745 A CN202011271745 A CN 202011271745A CN 112480871 A CN112480871 A CN 112480871A
Authority
CN
China
Prior art keywords
parts
change material
inorganic
phase
phase change
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.)
Pending
Application number
CN202011271745.3A
Other languages
Chinese (zh)
Inventor
曾祖铭
温伟东
温之行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenzhen Guoxin Energy Storage Technology Co ltd
Original Assignee
Shenzhen Guoxin Energy Storage Technology Co ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shenzhen Guoxin Energy Storage Technology Co ltd filed Critical Shenzhen Guoxin Energy Storage Technology Co ltd
Priority to CN202011271745.3A priority Critical patent/CN112480871A/en
Publication of CN112480871A publication Critical patent/CN112480871A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • 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
    • C09K5/063Materials absorbing or liberating heat during crystallisation; Heat storage materials

Abstract

The invention discloses an inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax and nano SiO21-2 parts of thickening agent, 11-15 parts of inorganic thickening agent, 4-10 parts of nano C powder and 120-170 parts of deionized water. The phase change temperature of the inorganic phase change material prepared by the invention is 5 ℃, the supercooling degree is 1.5 ℃, the phase change latent heat reaches 146.5KJ/KG, the inorganic phase change material can be recycled for more than 10000 times, the phase change process is reversible, the process is simple, the product recycling rate is high, the large-scale production can be realized, and the prepared inorganic phase change material is non-toxic and non-combustible, has high energy storage density, small volume, constant temperature control, obvious energy-saving effect, wide phase change temperature selection range and easy control.

Description

Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof
Technical Field
The invention relates to the technical field of preparation of inorganic phase change materials, in particular to an inorganic phase change material with a phase change temperature of 5 ℃ and a preparation method thereof.
Background
A Phase Change Material (PCM-Phase Change Material) refers to a substance that changes the state of a substance with a Change in temperature and can provide latent heat, and a process of changing a physical property is called a Phase Change process, and when the Phase Change Material absorbs or releases a large amount of latent heat. When the physical state changes, the temperature of the material itself is almost kept unchanged before the phase change is completed, a wide temperature platform is formed, although the temperature is unchanged, the latent heat absorbed or released is quite large, so the functions of the phase change material can be summarized as two points: constant temperature and energy storage, which are also dual properties of phase change materials. The common phase-change material is water, and the interconversion between liquid water and solid ice is a common phase-change process, but the ice volume is too large, so that the dissolving process needs a long time, and the latent heat provided is less, so that the ice phase-change material cannot be effectively and widely applied.
At present, phase-change materials are widely researched and applied in the fields of aviation, buildings, refrigeration equipment, communication, electric power and the like, for example: aviation aspect: by utilizing the constant temperature characteristic of the phase change material, the phase change material is applied to the space suit to help astronauts resist the environment temperature which is changed violently in space, so that the astronauts are in the temperature at which human beings normally live; the phase change material is applied to equipment such as a satellite, so that the equipment can be in a normal working temperature environment. In the aspect of refrigeration equipment: the refrigerating machine is mainly applied to equipment such as air conditioners, refrigerated vehicles, cold storages and the like, the traditional method utilizes the refrigerating machine to keep the temperature constant at a specific temperature required by the environment or the storage, utilizes the latent heat refrigerating principle of phase-change materials, can better meet the requirement in the aspect of refrigeration, and saves electric power.
Disclosure of Invention
The invention mainly aims at the problems in the prior art and provides an inorganic phase-change material with the phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Preferably, the thickener is one or a combination of more of carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol and polyvinylpyrrolidone.
Preferably, the inorganic thickener is one or a combination of more of diatomite, silica gel, sodium bentonite and attapulgite.
Preferably, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the latent heat of phase change is 146.5 KJ/KG.
Compared with the prior art, the invention has the beneficial effects that:
the phase change temperature of the inorganic phase change material prepared by the invention is 5 ℃, the supercooling degree is 1.5 ℃, the phase change latent heat reaches 146.5KJ/KG, the inorganic phase change material can be recycled for more than 10000 times, the phase change process is reversible, the process is simple, the product recycling rate is high, the large-scale production can be realized, and the prepared inorganic phase change material is non-toxic and non-combustible, has high energy storage density, small volume, constant temperature control, obvious energy-saving effect, wide phase change temperature selection range and easy control.
Drawings
FIG. 1 is a schematic flow chart of a process for preparing an inorganic phase-change material according to the present invention;
FIG. 2 is a graph of temperature control capability versus time for the inorganic phase change material of example 1 of the present invention;
FIG. 3 is a graph of recondensation temperature versus time for the inorganic phase change material of example 1 of the present invention.
Detailed Description
Example 1
As shown in the attached figure 1, an inorganic phase-change material with the phase-change temperature of 5 ℃ and a preparation method thereof are disclosed, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Specifically, the thickener is one or a combination of more of carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol and polyvinylpyrrolidone.
Specifically, the inorganic thickener is one or a combination of more of diatomite, silica gel, sodium bentonite and attapulgite.
Specifically, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
Example 2
An inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Specifically, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
Example 3
An inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Specifically, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
Comparative example 1
An inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Specifically, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
Comparative example 2
An inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof, wherein the inorganic phase-change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax, 11-15 parts of nano SiO 21-2 parts of thickening agent, 4-10 parts of inorganic thickening agent, 0.5 part of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: putting 10-20 parts of water into a preparation dish, sequentially adding the nano SiO2, the nano C powder, the thickening agent and the inorganic thickening agent into the preparation dish, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
Specifically, the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
Comparative example 3
Inorganic phase-change materials sold by other companies are adopted, the obtained supercooling degree is 1.5 ℃, and the phase-change latent heat is 146.5 KJ/KG.
As shown in fig. 2 and 3, recondensation refers to recondensation of the phase change material to start another energy absorption-release cycle, and the inorganic phase change material starts recondensation at 3.5 ℃, the condensation time is 7.5h, and is correspondingly shortened along with the reduction of the temperature, the condensation time at 3 ℃ is 6.5h, and the condensation time at 2 ℃ is 5 h.
When the environment temperature is 25 ℃, the temperature control capacity of the inorganic phase change material is inversely proportional to the time, the cold quantity released by the phase change material begins to decrease along with the increase of the time, the phase change material begins to release the cold quantity at 5 ℃, the temperature can be kept for 12 hours, and then the temperature is gradually increased until the phase change material is completely melted and is equal to the environment temperature.

Claims (4)

1. An inorganic phase-change material with a phase-change temperature of 5 ℃ and a preparation method thereof are characterized in that: the inorganic phase change material comprises the following components in parts by weight: 60-80 parts of sodium sulfate decahydrate, 12-25 parts of potassium chloride, 10-15 parts of ammonium chloride, 3-5 parts of sodium nitrate, 3-5 parts of borax and nano SiO2 1-2 parts of thickening agent, 11-15 parts of inorganic thickening agent, 4-10 parts of nano C powder and 120-170 parts of deionized water, wherein the preparation method of the inorganic phase-change material comprises the following specific steps:
the method comprises the following steps: placing 80-100 parts of water at 52-60 deg.C into a preparation vessel, slowly adding sodium sulfate decahydrate, stirring, and standing at constant temperature of 52-60 deg.C for 20-30 min to obtain solution A;
step two: sequentially putting potassium chloride, ammonium chloride, sodium nitrate and borax into a preparation dish, adding 30-50 parts of deionized water for dissolving, fully and uniformly mixing to obtain a solution B, slowly adding the solution B into the solution A, and continuously and uniformly stirring to obtain a solution C;
step three: taking 10-20 parts of water, putting the water into a preparation vessel, and adding nano SiO2Adding the nano C powder, the thickening agent and the inorganic thickening agent into a preparation vessel in sequence, and fully and uniformly stirring to obtain a solution D;
step four: and slowly adding the solution D into the solution C, uniformly stirring at the temperature of 70-90 ℃, keeping the constant temperature for 30-40 min, and naturally cooling to room temperature to obtain the inorganic phase change material.
2. The inorganic phase-change material with the phase-change temperature of 5 ℃ and the preparation method thereof as claimed in claim 1 are characterized in that: the thickening agent is one or a combination of more of carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol and polyvinylpyrrolidone.
3. The inorganic phase-change material with the phase-change temperature of 5 ℃ and the preparation method thereof as claimed in claim 1 are characterized in that: the inorganic thickener is one or a combination of more of diatomite, silica gel, sodium bentonite and attapulgite.
4. The inorganic phase-change material with the phase-change temperature of 5 ℃ and the preparation method thereof as claimed in claim 1 are characterized in that: the phase change temperature of the inorganic phase change material is 5 ℃, the supercooling degree is 1.5 ℃, and the phase change latent heat is 146.5 KJ/KG.
CN202011271745.3A 2020-11-13 2020-11-13 Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof Pending CN112480871A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011271745.3A CN112480871A (en) 2020-11-13 2020-11-13 Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011271745.3A CN112480871A (en) 2020-11-13 2020-11-13 Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof

Publications (1)

Publication Number Publication Date
CN112480871A true CN112480871A (en) 2021-03-12

Family

ID=74930676

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011271745.3A Pending CN112480871A (en) 2020-11-13 2020-11-13 Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112480871A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113214796A (en) * 2021-04-12 2021-08-06 东南大学 Composite inorganic salt phase change cold storage agent and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08218063A (en) * 1995-02-10 1996-08-27 Asahi Denka Kogyo Kk Latent heat-storing material composition
CN105038715A (en) * 2015-06-23 2015-11-11 江南大学 Hydrous salt cold storage agent with phase-transition temperature of 5-8 DEG C 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
CN107841292A (en) * 2017-09-29 2018-03-27 江苏理工学院 A kind of inorganic phase-changing material and its application
CN108300418A (en) * 2018-01-17 2018-07-20 松冷(武汉)科技有限公司 A kind of gel phase-change material and preparation method thereof, application process
CN109181653A (en) * 2018-10-09 2019-01-11 北京物资学院 Cold-storage material and application for the fresh cold chain transportation of fruits and vegetables

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08218063A (en) * 1995-02-10 1996-08-27 Asahi Denka Kogyo Kk Latent heat-storing material composition
CN105038715A (en) * 2015-06-23 2015-11-11 江南大学 Hydrous salt cold storage agent with phase-transition temperature of 5-8 DEG C 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
CN107841292A (en) * 2017-09-29 2018-03-27 江苏理工学院 A kind of inorganic phase-changing material and its application
CN108300418A (en) * 2018-01-17 2018-07-20 松冷(武汉)科技有限公司 A kind of gel phase-change material and preparation method thereof, application process
CN109181653A (en) * 2018-10-09 2019-01-11 北京物资学院 Cold-storage material and application for the fresh cold chain transportation of fruits and vegetables

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113214796A (en) * 2021-04-12 2021-08-06 东南大学 Composite inorganic salt phase change cold storage agent and preparation method thereof

Similar Documents

Publication Publication Date Title
CN104140786B (en) Composite phase-change thermal storage material
US4237023A (en) Aqueous heat-storage compositions containing fumed silicon dioxide and having prolonged heat-storage efficiencies
CN106753255B (en) Low-temperature phase-change material with phase-change temperature of-26 to-28 DEG C
CN105195068A (en) Preparation method of modified aerosil-based composite phase-change material
CN108676550B (en) Inorganic hydrated salt porous carbon composite phase change material and preparation method thereof
CN102660230A (en) Heat superconducting composite phase change energy storage material
CN107523272B (en) High-thermal-conductivity binary low-eutectic-temperature-coefficient hydrated salt phase-change material and preparation method thereof
CN105154021A (en) Highly heat-conducting phase change heat storage material and preparation method therefor
CN101747868B (en) Composite phase change energy storage material and preparation method thereof
CN112480871A (en) Inorganic phase-change material with phase-change temperature of 5 ℃ and preparation method thereof
CN104293304A (en) Solar heat accumulation type vacuum heat pipe, heat accumulation phase change material and preparation technology of heat accumulation phase change material
CN105154023A (en) Phase change cold-accumulation material and preparation method thereof
Man et al. Review on the thermal property enhancement of inorganic salt hydrate phase change materials
CN102268245B (en) Preparation method of room temperature inorganic phase-change material
CN101560376B (en) Shaped compound phase-change material and preparation method thereof
CN103468216B (en) A kind of Phosphate inorganic nano phase change energy storage material and preparation method thereof
CN114316915A (en) High-latent-heat low-supercooling low-temperature inorganic phase change energy storage material and preparation method thereof
CN103468220B (en) A kind of method reducing Inorganic nano phase change energy storage material fusing point
CN103484075A (en) Room-temperature inorganic nano phase-change energy storage material and preparation method thereof
CN104650815A (en) Composite figuration phase change cold-storage material and preparation method thereof
CN101974313B (en) Phase change thermal storage material and manufacturing method thereof
CN105154022A (en) Metal substrate highly heat-conducting heat storage material and preparation method therefor
CN105586011A (en) Inorganic hydrated salt phase-change heat-storage material and preparation method thereof
CN108822804A (en) A kind of phase-changing energy storage material and preparation method thereof encapsulated with porous material
CN103468218B (en) A kind of Inorganic nano phase change energy storage material and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination