CN107384325A - A kind of method for extending hydrous salt phase change material service life - Google Patents

A kind of method for extending hydrous salt phase change material service life Download PDF

Info

Publication number
CN107384325A
CN107384325A CN201710559907.5A CN201710559907A CN107384325A CN 107384325 A CN107384325 A CN 107384325A CN 201710559907 A CN201710559907 A CN 201710559907A CN 107384325 A CN107384325 A CN 107384325A
Authority
CN
China
Prior art keywords
change material
phase change
hydrous salt
service life
salt phase
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.)
Granted
Application number
CN201710559907.5A
Other languages
Chinese (zh)
Other versions
CN107384325B (en
Inventor
刘维桥
沈尧胤
郑成
王豪
邹超
潘君丽
周全法
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.)
Jiangsu University of Technology
Original Assignee
Jiangsu University of Technology
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 Jiangsu University of Technology filed Critical Jiangsu University of Technology
Priority to CN201710559907.5A priority Critical patent/CN107384325B/en
Publication of CN107384325A publication Critical patent/CN107384325A/en
Application granted granted Critical
Publication of CN107384325B publication Critical patent/CN107384325B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Thermotherapy And Cooling Therapy Devices (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

The invention discloses a kind of method for extending hydrous salt phase change material service life, phase-change material is placed under 20~30 DEG C lower than its freezing point of temperature atmosphere by this method to be solidified, apply the external condition of ultrasonic activation simultaneously, intense impact caused by low temperature range and vibration destroys original crystalline rate, crystal grain is refined, therefore higher heat of fusion is maintained, so as to extend the service life of phase-change material.The present invention need not add any other crystal and change agent, thickener etc., and the heat enthalpy value of phase-change material is maintained using physical method, extends its service life.The physical method that the invention need to only use, it is simple to operate, securely and reliably.

Description

A kind of method for extending hydrous salt phase change material service life
Technical field
The present invention relates to phase-change accumulation energy field, a kind of specific design to side for extending hydrous salt phase change material service life Method.
Background technology
Phase-change material (PCM-Phase Change Material) refers to vary with temperature and change state of matter and can carry For the material of latent heat.The process of transformation physical property is referred to as phase transition process, and at this moment phase-change material will absorb or release is substantial amounts of latent Heat.This material is once widely used in human lives, by as the optimal green carrier of energy-conserving and environment-protective, in China Sequence is utilized through being classified as national research and development.Phase-change material can be divided into organic (Organic) and inorganic (Inorganic) phase transformation material Material.Also hydrated salt (Hydrated Salts) phase-change material and wax (Paraffin Wax) phase-change material can be divided into.Hydrated salt Class phase transformation material is a kind of phase-change material important in middle low temperature accumulation of energy, it has, and use is extensive, cheap, heat of fusion is high, Many advantages, such as thermal conductivity is good.But in application process, there is also two outstanding problems, problem and phase separation is respectively subcooled in it Problem.When liquid is after multiple solidification dissolving circulation, crystal grain becomes big, just has partial crystals not molten during dissolving Solution, " rust " for hindering solid-liquid contact is formed, original inorganic salt crystal can not be formed, so as to fail.Addition thickener, crystal change The service life of phase-change material can be extended by becoming agent, but also increase cost simultaneously, and be added needed for different phase-change materials Reagent it is also different, sometimes as the increase of cycle-index, its service life can also have a greatly reduced quality.This method both can be in phase transformation It is that can also be used in phase-change material use that material, which makes, and physical method is safe and reliable, substantially increases hydrous salt phase transition material The application prospect of material.
The content of the invention
Present invention aims to overcome that above-mentioned the deficiencies in the prior art, there is provided a kind of physical method extends hydrous salt phase transition The service life of material.
To achieve the above object, the present invention adopts the following technical scheme that:
Phase-change material, which is placed under 20~30 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation Intense impact caused by external condition, low temperature range and vibration can destroy original crystalline rate, refine crystal grain, Therefore higher heat of fusion is maintained, so as to extend the service life of phase-change material.
Preferably, described hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240J/g~252J/g, By the Frozen-thawed cycled of 400~500 times, the heat enthalpy value of normal Frozen-thawed cycled falls below 141J/g~150J/g, heat content loss late Reaching 37%~44%, and use heat enthalpy value 212J/g~219J/g of the Frozen-thawed cycled of this method, heat content loss late is 8%~ 16%.
Preferably, described hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 218J/g~226J/g, By the Frozen-thawed cycled of 400~500 times, the heat enthalpy value of normal Frozen-thawed cycled falls below 112J/g~120J/g, heat content loss late Reach 44%~51%, and use heat enthalpy value 182J/g~194J/g of the Frozen-thawed cycled of this method, heat content loss late is 11% ~19%.
Preferably, described hydrous salt phase change material is 12 crystallization water aluminum sulfate, its initial heat enthalpy value be 257J/g~ 269J/g, by the Frozen-thawed cycled of 400~500 times, the heat enthalpy value of normal Frozen-thawed cycled falls below 164J/g~172J/g, heat content Loss late reaches 33%~39%, and uses heat enthalpy value 223J/g~232J/g of the Frozen-thawed cycled of this method, heat content loss late For 10%~17%.
The invention has the advantages that:
1st, need not add any other thickener and crystal change agent can extend the service life of hydrous salt phase change material.
2nd, method is simple, securely and reliably.
Embodiment
Presently in connection with embodiment, the present invention is further detailed explanation.
Embodiment 1:Hydrous salt phase change material sal glauberi extends the method and comparative experimental research in life-span:Respectively than Its freezing point is low 15 DEG C, 20 DEG C, 25 DEG C, 30 DEG C, solidify under 35 DEG C of temperature atmosphere, other conditions are identical, hotter break value Loss late, specific experiment are as follows:
(1) hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240.134J/g, and the phase-change material is put Solidified under 25 DEG C lower than its freezing point of temperature atmosphere, while apply the jelly that ultrasonic activation passes through 400 times using this method Melt circulation, its enthalpy drops to 214.278J/g, and the loss late of heat enthalpy value is 10.8%.
(2) hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240.134J/g, and the phase-change material is put Solidified under 20 DEG C lower than its freezing point of temperature atmosphere, while apply the jelly that ultrasonic activation passes through 400 times using this method Melt circulation, its enthalpy drops to 212.280J/g, and the loss late of heat enthalpy value is 11.6%.
(3) hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240.134J/g, and the phase-change material is put Solidified under 30 DEG C lower than its freezing point of temperature atmosphere, while apply the jelly that ultrasonic activation passes through 400 times using this method Melt circulation, its enthalpy drops to 203.634J/g, and the loss late of heat enthalpy value is 15.2%.
(4) hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240.134J/g, and the phase-change material is put Solidified under 15 DEG C lower than its freezing point of temperature atmosphere, while apply the jelly that ultrasonic activation passes through 400 times using this method Melt circulation, its enthalpy drops to 154.886J/g, and the loss late of heat enthalpy value is 35.5%.
(5) hydrous salt phase change material is sal glauberi, and its initial heat enthalpy value is 240.134J/g, and the phase-change material is put Solidified under 35 DEG C lower than its freezing point of temperature atmosphere, while apply the jelly that ultrasonic activation passes through 400 times using this method Melt circulation, its enthalpy drops to 177.699J/g, and the loss late of heat enthalpy value is 26.0%.
Case study on implementation 2:Hydrous salt phase change material Sodium acetate trihydrate extends the method and comparative experimental research in life-span:Exist respectively 15 DEG C lower than its freezing point, 20 DEG C, 25 DEG C, 30 DEG C, solidify under 35 DEG C of temperature atmosphere, other conditions are identical, hotter break value Loss late, specific experiment is as follows:
(1) hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 224.167J/g, and the phase-change material is put Solidified under 25 DEG C lower than its freezing point of temperature atmosphere, while apply ultrasonic activation use, passed through 450 times using this method Frozen-thawed cycled, its enthalpy drops to 183.153J/g, and the loss late of heat enthalpy value is 18.3%.
(2) hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 224.167J/g, and the phase-change material is put Solidified under 20 DEG C lower than its freezing point of temperature atmosphere, while apply ultrasonic activation use, passed through 450 times using this method Frozen-thawed cycled, its enthalpy drops to 186.955J/g, and the loss late of heat enthalpy value is 16.6%.
(3) hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 224.167J/g, and the phase-change material is put Solidified under 30 DEG C lower than its freezing point of temperature atmosphere, while apply ultrasonic activation use, passed through 450 times using this method Frozen-thawed cycled, its enthalpy drops to 177.092J/g, and the loss late of heat enthalpy value is 21.0%.
(4) hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 224.167J/g, and the phase-change material is put Solidified under 35 DEG C lower than its freezing point of temperature atmosphere, while apply ultrasonic activation use, passed through 450 times using this method Frozen-thawed cycled, its enthalpy drops to 138.759J/g, and the loss late of heat enthalpy value is 38.1%.
(5) hydrous salt phase change material is Sodium acetate trihydrate, and its initial heat enthalpy value is 224.167J/g, and the phase-change material is put Solidified under 15 DEG C lower than its freezing point of temperature atmosphere, while apply ultrasonic activation use, passed through 450 times using this method Frozen-thawed cycled, its enthalpy drops to 131.586J/g, and the loss late of heat enthalpy value is 41.3%.
Implementation case row 3:The crystallization water aluminum sulfate of hydrous salt phase change material 12 extends the method and comparative experimental research in life-span: Solidified respectively under 15 DEG C lower than its freezing point, 20 DEG C, 25 DEG C, 30 DEG C, 35 DEG C of temperature atmosphere, other conditions are identical, compare The loss late of hot break value, specific experiment are as follows:
(1) hydrous salt phase change material is 12 crystallization water aluminum sulfate, and its initial heat enthalpy value is 259.153J/g, by the phase transformation Material, which is placed under 25 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation use, is passed through using this method The Frozen-thawed cycled of 475 times is crossed, its enthalpy drops to 225.125J/g, and the loss late of heat enthalpy value is 13.1%.
(2) hydrous salt phase change material is 12 crystallization water aluminum sulfate, and its initial heat enthalpy value is 259.153J/g, by the phase transformation Material, which is placed under 30 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation use, is passed through using this method The Frozen-thawed cycled of 475 times is crossed, its enthalpy drops to 218.725J/g, and the loss late of heat enthalpy value is 15.6%.
(3) hydrous salt phase change material is 12 crystallization water aluminum sulfate, and its initial heat enthalpy value is 259.153J/g, by the phase transformation Material, which is placed under 20 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation use, is passed through using this method The Frozen-thawed cycled of 475 times is crossed, its enthalpy drops to 225.722J/g, and the loss late of heat enthalpy value is 12.9%.
(4) hydrous salt phase change material is 12 crystallization water aluminum sulfate, and its initial heat enthalpy value is 259.153J/g, by the phase transformation Material, which is placed under 35 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation use, is passed through using this method The Frozen-thawed cycled of 475 times is crossed, its enthalpy drops to 186.072J/g, and the loss late of heat enthalpy value is 28.2%.
(5) hydrous salt phase change material is 12 crystallization water aluminum sulfate, and its initial heat enthalpy value is 259.153J/g, by the phase transformation Material, which is placed under 15 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation use, is passed through using this method The Frozen-thawed cycled of 475 times is crossed, its enthalpy drops to 174.41J/g, and the loss late of heat enthalpy value is 32.7%.
From above experimental study:Three kinds of different hydrous salt phase change materials are respectively at 20 DEG C lower than its freezing point -- and 30 DEG C temperature atmosphere under solidify, in the case of other conditions identical, the loss late of hot break value is small, and its freezing point it is low 15 DEG C and Solidified under 35 DEG C of temperature atmosphere, hot break value illustrates the application's more relative to big of loss late of the setting temperature of the application Hydrous salt phase change material is respectively at 20 DEG C lower than its freezing point -- and the technical method solidified under 30 DEG C of temperature atmosphere has notable Beneficial effect.

Claims (6)

  1. A kind of 1. method for extending hydrous salt phase change material service life, it is characterised in that the phase-change material is put into than it Solidify at the low temperature of freezing point, constantly vibrated during solidification.
  2. 2. the method according to claim 1 for extending hydrous salt phase change material service life, it is characterised in that by the phase Change material, which is placed under 20~30 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation.
  3. 3. the method according to claim 2 for extending hydrous salt phase change material service life, it is characterised in that by the phase Change material, which is placed under 25 DEG C lower than its freezing point of temperature atmosphere, to be solidified, while applies ultrasonic activation.
  4. 4. as the method for the extension hydrous salt phase change material service life described in claim any one of 1-3, it is characterised in that:Institute The hydrous salt phase change material stated is sal glauberi.
  5. 5. as the method for the extension hydrous salt phase change material service life described in claim any one of 1-3, it is characterised in that institute The hydrous salt phase change material stated is Sodium acetate trihydrate.
  6. 6. as the method for the extension hydrous salt phase change material service life described in claim any one of 1-3, it is characterised in that institute The hydrous salt phase change material stated is 12 crystallization water aluminum sulfate.
CN201710559907.5A 2017-07-11 2017-07-11 Method for prolonging service life of hydrated salt phase change material Active CN107384325B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710559907.5A CN107384325B (en) 2017-07-11 2017-07-11 Method for prolonging service life of hydrated salt phase change material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710559907.5A CN107384325B (en) 2017-07-11 2017-07-11 Method for prolonging service life of hydrated salt phase change material

Publications (2)

Publication Number Publication Date
CN107384325A true CN107384325A (en) 2017-11-24
CN107384325B CN107384325B (en) 2021-01-19

Family

ID=60339219

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710559907.5A Active CN107384325B (en) 2017-07-11 2017-07-11 Method for prolonging service life of hydrated salt phase change material

Country Status (1)

Country Link
CN (1) CN107384325B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1987007630A1 (en) * 1986-06-04 1987-12-17 Edeco Holdings Limited Activation of phase change medium
US20050195469A1 (en) * 2004-03-02 2005-09-08 Van Brocklin Andrew L. Phase change electrophoretic imaging for rewritable applications
CN102504768A (en) * 2011-11-01 2012-06-20 东南大学 Method for reducing supercooling degree of hydrous salt phase change material
CN103205242A (en) * 2013-05-07 2013-07-17 中国科学院青海盐湖研究所 Phase change energy storage material for heat preservation at night and preparation method
CN103743275A (en) * 2014-01-20 2014-04-23 华北电力大学 Device and method for utilizing hydrated salt phase-change material to stabilize supercooling energy storage device and application
US20150152308A1 (en) * 2011-12-05 2015-06-04 Hyundai Motor Company Micro particle for thermal control material and device and method of producing the same using ultrasonic high-temperature vibration scheme

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1987007630A1 (en) * 1986-06-04 1987-12-17 Edeco Holdings Limited Activation of phase change medium
US20050195469A1 (en) * 2004-03-02 2005-09-08 Van Brocklin Andrew L. Phase change electrophoretic imaging for rewritable applications
CN102504768A (en) * 2011-11-01 2012-06-20 东南大学 Method for reducing supercooling degree of hydrous salt phase change material
US20150152308A1 (en) * 2011-12-05 2015-06-04 Hyundai Motor Company Micro particle for thermal control material and device and method of producing the same using ultrasonic high-temperature vibration scheme
CN103205242A (en) * 2013-05-07 2013-07-17 中国科学院青海盐湖研究所 Phase change energy storage material for heat preservation at night and preparation method
CN103743275A (en) * 2014-01-20 2014-04-23 华北电力大学 Device and method for utilizing hydrated salt phase-change material to stabilize supercooling energy storage device and application

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
崔文龙等: ""三水合乙酸钠在相变单元的传热特性及其过冷度改善"", 《化工学报》 *
金星 等: ""三水醋酸钠部分融化相变特性"", 《走中国创造之路-2011中国制冷学会年会论文集》 *

Also Published As

Publication number Publication date
CN107384325B (en) 2021-01-19

Similar Documents

Publication Publication Date Title
CN108467711B (en) Inorganic composite phase change material and preparation method thereof
CN100563871C (en) A kind of crystallizer protecting cinder for continuous casting of crack sensitive steel and preparation method thereof
CN102268241A (en) Phase transition material for cooling with phase transition temperature of 12-29 DEG C and preparation method thereof
CN107418521B (en) Ternary phase change cold storage material and preparation method thereof
WO2009041396A1 (en) Aqueous solution for clathrate hydrate formation, heat-storage agent, process for producing clathrate hydrate or slurry thereof, method of storing/radiating heat, and process for preparing aqueous solution for forming latent-heat-storage agent or major component thereof
CN204138818U (en) A kind of overflow for polycrystalline silicon ingot or purifying furnace is cotton
CN103801240B (en) Normal temperature prepares the method for phase transformation Nano capsule
CN109054763B (en) Hydrated sulfate composite phase-change material and preparation method thereof
CN107384325A (en) A kind of method for extending hydrous salt phase change material service life
Tang et al. Supercooling and phase separation of inorganic salt hydrates as PCMs
CN202591206U (en) Glass phase material hardening and crushing recovery device
CN102757100B (en) Method for improving production efficiency of vacuum crystallization for titaniferous solution
CN105086947A (en) Calcium chloride hexahydrate phase change energy storage material and preparation method therefor
CN106365520A (en) Energy-storage brick component and preparation method thereof
CN102796019A (en) Method for environment-friendly clean production of high-purity ethylene diamine tetraacetic acid (EDTA)
CN102617324B (en) Crystal size controllable continuous crystallization process of sodium acetate trihydrate
CN107075353A (en) The accumulator for power plant based on phase-change material (PCM)
CN202779668U (en) Waste heat recovery device of continuous casting secondary cooling section
CN106431023B (en) A kind of inexpensive activating process method of Boron Slag
CN105623618A (en) Inorganic hydrated salt composite phase change heat storage material and preparation method thereof
CN109135678B (en) Room temperature phase change energy storage material and preparation method thereof
CN115612454A (en) Binary inorganic phase change energy storage material and preparation method thereof
CN106431440B (en) A kind of micro- closed pore alumina refractory aggregate of light weight and preparation method thereof
JP2007314741A (en) Latent heat storage material composition
CN102786913A (en) Energy storage material composition of 58 DEG C

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
GR01 Patent grant
GR01 Patent grant