A novel UV‐cured interpenetrating organic–inorganic hybrid polymer network based phase change materials (IPN‐PCM)

The purpose of this paper is to introduce a novel UV‐cured interpenetrating polymer networked phase change materials (IPN‐PCMs), on which no article has been found in the so far published research. Maleated castor oil (MCO) was synthesized via maleinization reaction of castor oil with maleic anhydride. Organic–inorganic hybrid interpenetrating polymer networked (IPN) materials containing both cationic and radical sections and IPN‐PCMs containing tetradecanol, hexadecanol, and octadecanol were prepared. The chemical structure of MCO and organic–inorganic hybrid IPN‐PCMs were determined by using Fourier Transform Infrared Spectroscopy (FT‐IR). Differential scanning calorimetry (DSC) was used for examining the phase‐change behaviors of the materials. Thermal stability was investigated by thermogravimetric analysis (TGA). Moreover, the surface formation of the specimen was investigated by scanning electron microscopy (SEM). In conclusion, our study proved that because of their high latent heat storage scope and high thermal stability, the obtained organic–inorganic hybrid IPN‐PCMs could be used as thermal energy storage materials. POLYM. ENG. SCI., 58:870–875, 2018. © 2017 Society of Plastics Engineers     

Novel semi‐interpenetrating network structural phase change composites with high phase change enthalpy

High phase change enthalpy, controllable temperature, and stable shape can expand the application of phase change materials (PCMs) in energy storage. In this study, a series of novel form‐stable PCMs with high phase change enthalpy (169–195 J/g) and controllable temperature (45.3–61.4°C) were prepared. The PCMs exhibited a semi‐interpenetrating polymer network (semi‐IPN) structure resulting from the combination of polyethylene glycol (PEG) and a three‐dimensional (3‐D) network gel. The gel itself featured an inherent phase change characteristic and a 3‐D network structure. Thus, it improved the phase transition enthalpy of the materials and facilitated the formation of a semi‐IPN that endowed the materials with excellent form‐stable properties. In addition, the latent heat of the composites (169–195 J/g) is much higher than most of the previously reported composites using PEG as phase change component (68–132 J/g). © 2017 American Institute of Chemical Engineers AIChE J, 64: 688–696, 2018     

Preparation and thermal energy storage properties of poly(n‐butyl methacrylate)/fatty acids composites as form‐stable phase change materials

This work is focused on the preparation, characterization, and determination of thermal energy storage properties of poly(n‐butyl methacrylate) (PnBMA)/fatty acid composites as form‐stable phase change material (PCM). In the composite materials, the fatty acids act as latent heat storage material whereas PnBMA serves as supporting material, which prevents the leakage of the melted fatty acids. The maximum encapsulation ratio for all fatty acids was found to be 40 wt%. The composites that do not allow PCM leakage in melted state were identified as form‐stable PCMs. The compatibility of fatty acids with PnBMA is investigated by optical microscopy (OM) and Fourier Transform Infrared (FT‐IR) spectroscopy. Thermal properties and thermal reliability of the form‐stable composite PCMs were determined using differential scanning calorimetry (DSC). DSC analysis revealed that the form‐stable composite PCMs had melting temperatures between 29.62°C and 53.73°C and latent heat values between 67.23 J/g and 87.34 J/g. Thermal stability of the composite PCMs was studied by thermal gravimetric (TG) analysis and the results indicated that the form‐stable PCMs had good thermal stability. In addition, thermal cycling test showed that the composite PCMs had good thermal reliability with respect to the changes in their thermal properties after accelerated 5,000 thermal cycling. On the basis of all results, it was also concluded that the prepared form‐stable composite PCMs had important potential for many thermal energy storage applications such as solar space heating of buildings by using wallboard, plasterboard or floors integrated with PCM. POLYM. COMPOS., 2012. © 2011 Society of Plastics Engineers     

Poly(ethylene glycol)/poly(methyl methacrylate) blends as novel form‐stable phase‐change materials for thermal energy storage

In this study, we focused on the preparation and characterization of poly(ethylene glycol) (PEG)/poly(methyl methacrylate) (PMMA) blends as novel form‐stable phase‐change materials (PCMs) for latent‐heat thermal energy storage (LHTES) applications. In the blends, PEG acted as a PCM when PMMA was operated as supporting material. We subjected the prepared blends at different mass fractions of PEG (50, 60, 70, 80, and 90% w/w) to leakage tests by heating the blends over the melting temperature of the PCM to determine the maximum encapsulation ratio without leakage. The prepared 70/30 w/w % PEG/PMMA blend as a form‐stable PCM was characterized with optical microscopy and Fourier transform infrared spectroscopy. The thermal properties of the form‐stable PCM were measured with differential scanning calorimetry (DSC). DSC analysis indicated that the form‐stable PEG/PMMA blend melted at 58.07°C and crystallized at 39.28°C and that it had latent heats of 121.24 and 108.36 J/g for melting and crystallization, respectively. These thermal properties give the PCMs potential LHTES purposes, such as for solar space heating and ventilating applications in buildings. Accelerated thermal cycling tests also showed that the form‐stable PEG/PMMA blend as PCMs had good thermal reliability and chemical stability. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Solid–solid phase‐change materials based on hyperbranched polyurethane for thermal energy storage

A hyperbranched polyol (HBP) was synthesized with poly(ethylene glycol) (PEG) as the core molecule and 2,2‐bis(hydroxymethyl) propionic acid as the chain extender. Then, a series of hyperbranched polyurethane phase‐change materials (HP‐PCMs) with different crosslinking densities was synthesized with isophorone diisocyanate and HBP as a molecular skeleton and PEG 6000 as a phase‐change ingredient. ¹H‐NMR, gel permeation chromatography, and Fourier transform infrared spectroscopy confirmed the successful synthesis of the HBP and HP‐PCMs. The polarization optical microscopy and wide‐angle X‐ray diffraction results show that the HP‐PCM exhibited good crystallization properties, but the crystallinity was lower than that of PEG 6000. The analysis results from differential scanning calorimetry indicated that the HP‐PCMs were typical solid–solid phase‐change materials with suitable phase‐transition temperatures. In addition, HP‐PCM‐3, with an appropriate degree of hyperbranched structure, possessed the highest thermal transition enthalpy of 123.5 J/g. Moreover, thermal cycling testing and thermogravimetric analysis showed that the HP‐PCMs exhibited good thermal reliability and stability. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45014.     

Poly(2‐alkyloyloxyethylacrylate) and poly(2‐alkyloyloxyethylacrylate‐co‐methylacrylate) comblike polymers as novel phase‐change materials for thermal energy storage

A series of poly(2‐alkyloyloxyethylacrylate) and poly(2‐alkyloyloxyethylacrylate‐co‐methylacrylate) polymers as novel polymeric phase‐change materials (PCMs) were synthesized starting from 2‐hydroxyethylacrylate and fatty acids. The chemical structure and crystalline morphology of the synthesized copolymers were characterized with Fourier transform infrared and ¹H‐NMR spectroscopy and polarized optical microscopy, respectively, and their thermal energy storage properties and thermal stability were investigated with differential scanning calorimetry and thermogravimetric analysis, respectively. The thermal conductivities of the PCMs were also measured with a thermal property analyzer. Moreover, thermal cycling testing showed that the copolymers had good thermal reliability and chemical stability after they were subjected to 1000 heating/cooling cycles. The synthesized poly(2‐alkyloyloxyethylacrylate) polymers and poly(2‐alkyloyloxyethylacrylate‐co‐methylacrylate) copolymers as novel PCMs have considerable potential for thermal energy storage and temperature‐control applications. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Thermal and Phase Change Material Properties of Comb-Like Polyacrylic Acid-Grafted-Fatty Alcohols

Poly(acrylic acid)-graft-fatty alcohol are synthesized from the esterification of polyacrylic acid with octadecanol and docosanol. The characterization of poly(acrylic acid)-graft-fatty alcohol was performed by attenuated total reflection–Fourier transform infrared spectroscopy. The thermal stability performances and phase change behaviors of poly(acrylic acid)-graft-fatty alcohol were examined by using thermogravimetric analysis system and differential scanning calorimetry. The results indicate that the poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials possess good phase change properties and provide a suitable working temperature range. The heating process phase change enthalpy is measured between 112 and 122?J g^?1, and the freezing process phase change enthalpy is found between 118 and 126?J g^?1. The decomposition of poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials started at 177°C and reached a maximum of 380°C. All of the obtained poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials improved latent heat storage capacity in comparison with the pristine poly(acrylic acid) polymer. With the obtained results we conclude that, these materials promise a great potential in thermal energy storage applications.     

Phase change material with flexible crosslinking for thermal energy storage

The utilization of renewable energy through phase change materials (PCMs) is particularly attractive for the realization of sustainable society. Herein, a flexible but reliable solid–solid PCM was successfully synthesized by the integration of quadruple H-bonding crosslinks with polyethylene glycol (PEG)-based polyurethanes. The strong quadruple H-bonding from the dimerization of 2-ureido-4 [1H]-pyrimidinone (UPy) units could act as dynamic cross-links to maintain shape stability. PEG chains in flexible polymer network serve as phase change ingredients, affording thermal energy storage capacity. The physical crosslink density and phase change enthalpy can be adjusted. In contrast to chemical crosslinks, the physical crosslinks of UPy provide reprocessability of the prepared PCMs and show little hindrance on the crystallization of PEG chains. The chemical structure, phase transformation, crystallization, and thermal properties of prepared PCMs were characterized by fourier transform infrared spectroscopy, differential scanning calorimetry (DSC), X-ray diffraction, polarizing microscope, and thermogravimetric analysis. DSC analysis shows that the prepared PCM can store 101.9 J g⁻¹ when PCMs undergo phase change process. Moreover, the accelerated thermal cycling test and leakage test are also conducted to illustrate the thermal reliability and shape-stable properties. These PCMs that possess high phase change enthalpy and outstanding reprocessability are alternative for solar energy collection and waste heat recovery. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48497.     

Poly(polyethylene glycol methyl ether methacrylate) as novel solid-solid phase change material for thermal energy storage

Poly(polyethylene glycol methyl ether methacrylate) as novel solid–solid phase change materials (PCMs) for thermal energy storage was prepared via the facile bulk polymerization of polyethylene glycol methyl ether methacrylate and was characterized by Fourier transform infrared, ¹³C-NMR, X-ray diffraction, differential scanning calorimetry, and thermogravimetric analysis measurements. Based on the results, it is indicated that the poly (polyethylene glycol methyl ether methacrylate) as novel PCM showed solid–solid properties with suitable transition temperature, high transition enthalpy, and good thermal stability, which was apt to crystallize due to the flexibility of long polyether side chain. This novel PCMs have advantages for the potential application in energy storage. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Development of heat storage gypsum board with paraffin-based mixed SSPCM for application to buildings

Latent heat thermal energy storage using phase change materials (PCMs) is considered to be the method with the most potential to solve the energy shortage problem. In this study, paraffin-based mixed shape-stabilized PCM (SSPCM) (PBMS) was made by vacuum impregnation method. The prepared PBMS was added to gypsum powder as a fine aggregate. In the experiment, the n-hexadecane and n-octadecane was used as the PCM and the materials have latent heat capacities of 254.7 and 247.6 J/g, and melting points of 20.84 and 30.4 °C, respectively. The PBMS was prepared by an impregnation method in a vacuum, following the manufacturing process. The physical and thermal properties of the PBMS gypsum board were analyzed by Fourier transform infrared spectrometry (FTIS), differential scanning calorimetry, enthalpy analysis, and thermogravimetric analysis. From the Fourier transform infrared analysis, PBMS could be maintained in the structure of the gypsum board due to its physical rather than chemical bonding. From the specific heat and enthalpy analysis, the PBMS has high enthalpy and thermal inertia property. In addition, the gypsum board with PBMS has high latent heat capacity and high thermal efficiency.     

Preparation,thermal properties and thermal reliability of eutectic mixtures of fatty acids/expanded vermiculite as novel form-stable composites for energy storage

This paper deals with the preparation, characterization, thermal properties and thermal reliability of novel form-stable composite phase change materials (PCMs) composed of eutectic mixtures of fatty acids and expanded vermiculite for thermal energy storage. The form-stable composite PCMs were prepared by incorporation of eutectic mixtures of fatty acids (capric–lauric, capric–palmitic and capric–stearic acids) within the expanded vermiculite by vacuum impregnation method. The composite PCMs were characterized by SEM and FTIR techniques. Thermal properties of the composite PCMs were determined by differential scanning calorimeter (DSC) method. DSC results showed that the melting temperatures and latent heats of the prepared composite PCMs are in the range of 19.09–25.64 °C and 61.03–72.05 J/g, respectively. The thermal cycling test including 5000 heating and cooling process was conducted to determine the thermal reliability of the composite PCMs. The test results showed that the composite PCMs have good thermal reliability and chemical stability. Furthermore, thermal conductivities of the composite PCMs were increased by adding 10 wt% expanded graphite. Based on all results, the prepared form-stable composites can be considered as promising PCMs for low temperature thermal energy storage applications due to their satisfactory thermal properties, good thermal reliability, chemical stability and thermal conductivities.     

Preparation and characterization of di‐hexadecanol maleic/triallyl isocyanurate cross‐linked copolymer as solid–solid phase change materials

Di‐hexadecanol maleic/Triallyl isocyanurate cross‐linked copolymers as a novel solid–solid phase change materials were successfully synthesized through bulk polymerization. TAIC is the skeleton and DM is a functional side chain that stores and releases heat during its phase transition process. Fourier transform infrared spectroscopy, wide‐angle X‐ray diffraction, polarizing optical microscopy, differential scanning calorimetry, and thermogravimetry were employed to study the composition, chemical structure, crystalline properties, phase transition behaviors, and the thermal stability of the cross‐linked copolymers, respectively. The test results indicate that DM/TAIC cross‐linked copolymers have good thermal reliability and heat storage durability after 500 thermal cycles. The phase change temperatures of DM/TAIC cross‐linked copolymers were approximately 28.24–37.02°C, and it has high latent heat storage capacity of more than 83 J/g. At the same time, DM/TAIC cross‐linked copolymers have good thermal stability, and they can be processed or used in high temperature environments. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44065.     

Polymeric phase change composites for thermal energy storage

This article describes a group of thermal energy storage (TES) composites that combine TES and structural functionality. The composites are encapsulations of low melt temperature phase change materials (PCM) such as paraffin waxes in polymer matrices. Room temperature cured bisphenol‐A epoxy and styrene–ethylene–butylene–styrene (SEBS) polymers are chosen as matrix materials because of their excellent chemical and mechanical properties. The polymeric network structure in the composite encapsulates the PCMs, which transform from the solid to the liquid phase. The PCMs provide the energy storage function via the solid–liquid latent heat effect. The resulting composite exhibits dry‐phase transition in the sense that fluid motion of the PCM, when in the liquid phase, is inhibited by the structure of the polymer matrix. The polymer matrix is formulated to provide structural functionality. The latent heat, thermal conductivity and contact conductance, and structural moduli of composites having various PCM‐to‐matrix volume fractions are measured. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1240–1251, 2004     

Eudragit S (methyl methacrylate methacrylic acid copolymer)/fatty acid blends as form‐stable phase change material for latent heat thermal energy storage

By composing (Eudragit S) with fatty acids (stearic acid (SA), palmitic acid (PA), and myristic acid (MA)), form‐stable phase change materials (PCMs), which can retain the same shape in a solid state even when the temperature of the PCMs is over the melting points of the fatty acids, are prepared. The compatibility of fatty acids with the Eudragit S is proved by microscopic investigation and infrared (FTIR) spectroscopy. The melting and crystallization temperatures and the latent heats of melting and crystallization of the form‐stable PCMs are measured by Differential Scanning Calorimetry (DSC) method. The maximum mass percentage of all fatty acids in the form‐stable PCMs is found as 70%, and no leakage of fatty acid is observed at the temperature range of 50–70°C for several heating cycles. Thermal properties obtained from the DSC analysis indicate that the Eudragit S/fatty acid blends as form‐stable PCM have great potential for passive solar latent heat thermal energy storage (LHTES) applications in terms of their satisfactory thermal properties and utility advantage. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1402–1406, 2006     

New biobased carboxylic acid hardeners for epoxy resins

Soybean oil was modified into a novel biobased polyacid hardener by thiol‐ene coupling with thioglycolic acid. The structure of the initial soybean oil and polyacid triglyceride was carefully analyzed using ¹H NMR and titration. The thermal crosslinking reaction between acid hardener and epoxidized resin was studied by differential scanning calorimetry (DSC) and rheology. Then, the synthesized biobased acid hardener was employed as a novel curing agent for bisphenol A diglycidyl ether to elaborate new partially biobased materials. These materials, formulated in stoichiometry ratio, were characterized by DSC, thermogravimetry analyses, dynamic mechanical analyses and exhibit interesting properties for coatings. Practical applications: The products of the chemistry described in this contribution, i.e., polyacid from soybean oil and thioglycolic acid, provide biobased building blocks for further epoxy resin syntheses by reaction with epoxy groups. The obtained epoxy resins are partially biobased and may be applied as binders and coatings.     

Mechanical properties and thermal stability of double‐shell thermal‐energy‐storage microcapsules

Double‐shell‐structured microcapsules encapsulating phase‐change materials (micro‐PCMs) with an average diameter of 5–10 μm were successfully fabricated with a melamine–formaldehyde resin as the coating material. The mechanical properties of the obtained piled micro‐PCMs, tested under compression, were evaluated with a pressure sensor. Typical stress–strain curves showed that both the single‐shell‐ and double‐shell‐structured microcapsules had yield points and maximum point pressures. The morphological changes in the shell surface confirmed the existence of yield points by scanning electron microscopy. When the pressure was beyond the yield point, the microcapsules showed conventional plastic behavior, and the double‐shell structure was more mechanically stable than the single‐shell one. Differential scanning calorimetry analysis results revealed that the properties of the phase‐change materials experienced no variation after coating with a single‐shell‐ or double‐shell‐structured polymer. Thermogravimetric analysis showed that the double‐shell‐structured micro‐PCMs experienced a weight loss of only about 5% from 86.3 to 232°C but did so more rapidly from 232 to 416°C. Thermoregulation was determined with periodical heating and cooling tests. The data showed that the micro‐PCMs changed temperature in a narrow range of 20–25°C with a time lag of 20 min to reach the maximum or minimum temperature in comparison with a reference temperature of 18–28°C. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1295–1302, 2007     

ESOA modified unsaturated polyester hybrid networks: A new perspective

Hybrid polymer networks based on unsaturated polyester (UPE) and epoxidized soybean oil acrylate (ESOA) were synthesized by reactive blending through free radical addition polymerization reaction. ESOA was prepared by acrylation of epoxidized soybean oil (ESO). The physical, mechanical, thermal and electrical properties of the cured blends were compared with the neat resin. ESOA resin bearing reactive functional groups showed good miscibility and compatibility with the UPE resin. The co‐cured resin showed substantial upgrading in the toughness, impact resistance, thermal properties, and downgrading brittleness up to the addition of 20 wt % of ESOA content. The muddled phase structure was corroborated by Fourier transform infrared spectroscopy, scanning electron microscope, and transmission electron microscopy and proved the formation of excellent hybrid polymer network. An improvement in overall properties has been achieved without seriously affecting any other properties. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44345.     

铜纳米粒子导热增强固-液相变储能材料的性能

使用聚乙烯吡咯烷酮（PVP）和聚乙二醇（PEG）作为钝化剂对铜纳米颗粒进行原位包覆制备了PVP/PEG/Cu复合纳米粒子（CuNP），将其作为导热增强剂引入到PEG中制备了CuNP/PEG固-液相变储能材料（PCMs），并通过FTIR、XRD、DSC以及TGA等表征了CuNP/PEG固-液PCMs的结构及热性能。利用纳米粒子表面的PVP与PEG之间的氢键和空间位阻效应，以及PVP对铜核的保护作用，赋予了铜纳米粒子在PCMs中优异的分散稳定性。结果表明，CuNP的引入能够显著提高复合相变储能材料的导热能力，并能够作为晶核加速材料的结晶行为。当纳米粒子的质量分数为5%时，CuNP/PEG固-液PCMs的相变焓值为157.0 J/g，体系的储热速率、放热速率和结晶速率与纯PEG相比分别提高了34.09%、31.45%和53.33%。     

Latentwärmespeicher: Speichermaterialien,Wärmeübertragung und Anwendungen

Phase change materials (PCMs) can absorb/release heat during the phase change. They are frequently used in thermal storage systems due to their large latent heat und isothermal nature. This paper provides an overview of the various inorganic and organic PCMs. Techniques for improving their thermophysical properties and the corrosion of metallic construction materials by inorganic PCMs are discussed. Finally, typical applications for latent‐heat storage systems are presented.     

The use of lipids as phase change materials for thermal energy storage

Phase change materials (PCMs) are substances capable of absorbing and releasing large amounts of thermal energy (heat or cold) as latent heat at constant temperature as they undergo a change in state of matter (phase transition), commonly, between solid and liquid phases. Since the late 1940s, researchers have recognized the potential for phase change materials to play an essential part in energy storage systems and the search for suitable substances has received increasing interest. Currently, the global PCM market is estimated to grow from $ 460 million in 2013 to approximately $ 1.15 billion by 2018. Fats, oils, and their derivatives are diverse in their structures and among the few renewable feedstocks available that have melting and enthalpy profiles among other properties comparable to those of commercial paraffin waxes currently used in PCM applications. This has led to the investigation of triglycerides, fatty acids, esters, alcohols, and other lipid‐based derivatives as potential PCMs and much research examining lipid‐based materials as PCMs has been published. This article gives a brief overview of phase change materials, highlights the various types of lipid substances examined for PCM applications, and suggests potential future areas of study.