Galactitol hexa stearate and galactitol hexa palmitate as novel solid-liquid phase change materials for thermal energy storage

Galactitol has a melting point of 187.41 °C and a fusion enthalpy of 401.76 J g⁻¹. Its melting temperature is not suitable for many thermal energy storage applications although it has good latent heat storage capacity compared to the several traditional phase change materials (PCMs). The galactitol also has high supercooling degree as about 72 °C. These unfavorable properties limit the usage potential of galactitol in thermal energy storage applications. However, the phase change temperature and supercooling degree of galactitol can be reduced to a reasonable value and therefore its feasibility for energy storage systems can be increased. For this aim, in this study, galactitol hexa stearate (GHS) and galactitol hexa palmitate (GHP) were prepared as novel solid-liquid PCM by means of esterification reaction of the galactitol with palmitic acid and stearic acid. The GHP and GHS esters were characterized chemically using FT-IR and ¹H NMR techniques. By using DSC analysis method, the melting temperature and latent heat value of the PCMs were determined as 31.78 °C and 201.66 J g⁻¹ for GHP ester and 47.79 °C and 251.05 J g⁻¹ for GHS ester. Thermal cycling test showed that the prepared PCMs had good thermal reliability after thermal 1000 melting-freezing cycles. Thermogravimetric analysis (TGA) results revealed that the PCMs have good thermal stability over their working temperatures. In addition, thermal conductivity of the prepared PCMs was increased as about 26.3% for GHP and 53.3% for GHS by addition of 5 wt.% expanded graphite. Based on all results it can be concluded that the prepared GHP and GHS esters can be considered as promising solid-liquid PCMs for many energy storage applications such as solar energy storage, indoor temperature controlling in buildings, production of smart textile and insulation clothing due to their good energy storage properties.     

Energy balance model of combined photovoltaic solar-thermal system incorporating phase change material

In this paper an energy balance model and simulation results are presented for a generic combined photovoltaic (PV) solar thermal (ST) system that incorporates phase change material (PCM). This is a promising integration of technology because the PV converts visible and ultra-violet parts of the solar spectrum, the ST utilises infra-red parts of the spectrum and waste heat from the PV, and the PCM reduces the temperature of the PV which increases PV efficiency. Parameters that are investigated cover PCM physical and thermal properties and water flow schemes. By including an appropriate PCM in an optimised system, the PV output can be increased by typically 9% with an average water temperature rise of 20 °C. Although any increase in PV performance has an associated decrease in ST performance, a practical and worthwhile compromise can still be achieved. This paper demonstrates that there is considerable scope for experimental realisation of the combined PV/ST/PCM system particularly if this is coupled with the development of PCMs with tuneable melting points and high thermal conductivity.     

Self regulation of photovoltaic module temperature in V-trough using a metal-wax composite phase change matrix

The present study was carried out to take advantage of the enhanced solar insolation in V-trough while limiting the temperature of the photovoltaic (PV) module at around the maximum (ca. 65 °C) observed for conventional usage without any concentration. Paraffin wax of 56-58 °C melting range was chosen as phase change material (PCM) and incorporated at the rear of the module to absorb the excess heat. The problem of low thermal conductivity of the wax was solved with the help of packed metal turnings wherein the wax resided. Two sets of experiments were performed indoor and outdoor. Employing a 0.06 m thick bed of the PCM matrix, the module temperature in the indoor experiment could be maintained at 65-68 °C for 3 h whereas in its absence the temperature rose beyond 90 °C within 15 min. In outdoor studies, the module temperature in V-trough could be reduced from 78 °C to 62 °C with the PCM assembly and operation could be sustained throughout the day. Using the V-trough PV-PCM system, the output power over the day could be enhanced 1.55 times with self regulation of temperature. The molten wax formed during operation re-solidified during the evening and night and could be re-used. A significant finding was the safe operation of the module even under low wind velocity conditions without sacrificing operational simplicity.     

High latent heat storage and high thermal conductive phase change materials using exfoliated graphite nanoplatelets

Using exfoliated graphite nanoplatelets (xGnP), paraffin/xGnP composite phase change materials (PCMs) were prepared by the stirring of xGnP in liquid paraffin for high electric conductivity, thermal conductivity and latent heat storage. xGnP of 1, 2, 3, 5 and 7 wt% was added to pure paraffin at 75 °C. Scanning electron microscopy (SEM) morphology showed uniform dispersion of xGnP in the paraffin wax. Good dispersion of xGnP in paraffin/xGnP composite PCMs led to high electric conductivity. The percolation threshold of paraffin/xGnP composite PCMs was between 1 and 2 wt% in resistivity measurement. The thermal conductivity of paraffin/xGnP composite PCMs was increased as xGnP loading contents. Also, reproducibility of paraffin/xGnP composite PCMs as continuous PCMs was manifested in results of electric and thermal conductivity. Paraffin/xGnP composite PCMs showed two peaks in the heating curve by differential scanning calorimeter (DSC) measurement. The first phase change peak at around 35 °C is lower and corresponds to the solid-solid phase transition of the paraffin, and the second peak is high at around 55 °C, corresponding to the solid-liquid phase change. The latent heat of paraffin/xGnP composite PCMs did not decrease as loading xGnP contents to paraffin. xGnP can be considered as an effective heat-diffusion promoter to improve thermal conductivity of PCMs without reducing its latent heat storage capacity in paraffin wax.     

The effect of using two PCMs on the thermal regulation performance of BIPV systems

Building Integrated Photovoltaics (BIPVs) is one of the most promising applications for Photovoltaics (PVs). However, when the temperature in the BIPV increases, the conversion efficiency deteriorates. A PV/PCM system using Phase Change Materials (PCM) for BIPV thermal control has been experimentally and numerically studied previously. One of the main barriers for this application is how to improve the low thermal conductivity of the PCM in order to achieve a quick thermal dissipation response with longer thermal regulation in PVs. Although the metal fins inserted inside the PCM can improve the heat transfer, the thermal regulation period declines as the volume of the PCM is substituted by the metal mass of the PV/PCM system. A modified PV/PCM system integrated with two PCMs with different phase transient temperatures for improving the heat regulation needs to be investigated. The use of combinations of PCMs, each with a set of different phase transient temperatures, is expected to enhance the thermal regulation effect of the PV/PCM system and lengthen the thermal regulation time in PVs. In this study a developed PV/PCM numerical simulation model for single PCM application has been modified to predict the thermal performance of the multi-PCMs in a triangular cell in the PV/PCM system. A series of numerical simulations tests have been carried out in static state and realistic conditions in UK. The thermal regulation of the PV/PCM system with a different range of phase transient temperature PCMs has been discussed.     

Exergy analysis of two phase change materials storage system for solar thermal power with finite-time thermodynamics

A mathematical model for the overall exergetic efficiency of two phase change materials named PCM1 and PCM2 storage system with a concentrating collector for solar thermal power based on finite-time thermodynamics is developed. The model takes into consideration the effects of melting temperatures and number of heat transfer unit of PCM1 and PCM2 on the overall exergetic efficiency. The analysis is based on a lumped model for the PCMs which assumes that a PCM is a thermal reservoir with a constant temperature of its melting point and a distributed model for the air which assumes that the temperature of the air varies in its flow path. The results show that the overall exergetic efficiency can be improved by 19.0-53.8% using two PCMs compared with a single PCM. It is found that melting temperatures of PCM1 and PCM2 have different influences on the overall exergetic efficiency, and the overall exergetic efficiency decreases with increasing the melting temperature of PCM1, increases with increasing the melting temperature of PCM2. It is also found that for PCM1, increasing its number of heat transfer unit can increase the overall exergetic efficiency, however, for PCM2, only when the melting temperature of PCM1 is less than 1150 K and the melting temperature of PCM2 is more than 750 K, increasing the number of heat transfer unit of PCM2 can increase the overall exergetic efficiency. Considering actual application of solar thermal power, we suggest that the optimum melting temperature range of PCM1 is 1000-1150 K and that of PCM2 is 750-900 K. The present analysis provides theoretical guidance for applications of two PCMs storage system for solar thermal power.     

High-chain fatty acid esters of myristyl alcohol with odd carbon number: Novel organic phase change materials for thermal energy storage—2

A series of high-chain fatty acid esters of 1-tetradecanol (myristyl alcohol) were synthesized via esterification of 1-tridecanoic, 1-pentadecanoic, 1-heptadecanoic and 1-nonadecanoic acids under vacuum and in the absence of catalyst. The esterification reactions were controlled by FT-IR spectroscopy. Differential scanning calorimeter (DSC) and thermo-gravimetric analyzer (TGA) were intensively used to determine the thermal properties of the presented novel organic phase change materials (PCM). The thermal properties were given in terms of phase change temperature, enthalpy, specific heat (C_p) and thermal decomposition temperature with related statistical calculations. The thermal reliability of the synthesized PCMs, which is an important property for utilization, was determined via measuring the change in thermal properties after 1000 thermal cycles. The DSC analyses indicated that the melting points of the novel organic PCMs were between 40 and 50 °C with phase change enthalpy above 200 kJ/kg. The results showed that these thermal storage materials were favorable for low temperature heat transfer applications with superior thermal properties and reliability among the known PCMs.     

Highly conductive composites made of phase change materials and graphite for thermal storage

Conventional phase change materials (PCMs) are already well known for their high thermal capacity and constant working temperature for thermal storage applications. Nevertheless, their low thermal conductivity (around 1 W m⁻¹ K⁻¹) leads to low and decreasing heat storage and discharge powers. Up to now, this major drawback has drastically inhibited their possible applications in industrial or domestic fields. The use of graphite to enhance the thermal conductivity of those materials has been already proposed in the case of paraffin but the corresponding applications are restricted to low-melting temperatures (below 150 °C). For many applications, especially for solar concentrated technologies, this temperature range is too low. In the present paper, new composites made of salts or eutectics and graphite flakes, in a melting temperature range of 200-300 °C are presented in terms of stability, storage capacity and thermal conductivity. The application of those materials to thermal storage is illustrated through simulated results according to different possible designs. The synergy between the storage composite properties and the interfacial area available for heat transfer with the working fluid is presented and discussed.     

Analysis of thermal and electrical performance of semi-transparent photovoltaic (PV) module

Building-integrated PhotoVoltaic (BIPV) is one of the most fascinating PV application technologies these days. To apply PV modules in buildings, various factors should be considered, such as the installation angle and orientation of PV module, shading, and temperature. The temperature of PV modules that are attached to building surfaces especially is one of the most important factors, as it affects both the electrical efficiency of a PV module and the energy load in a building. This study investigates the electrical and thermal performance of a semi-transparent PV module that was designed as a glazing component. The study evaluates the effects of the PV module's thermal characteristics on its electrical generation performance. The experiment was performed under both Standard Test Condition (STC) and outdoor conditions. The results showed that the power decreased about 0.48% (in STC with the exception of the temperature condition) and 0.52%(in outdoor conditions, under 500 W/m²) per the 1 °C increase of the PV module temperature. It was also found that the property of the glass used for the module affected the PV module temperature followed by its electrical performance.     

Cellulose-based solid-solid phase change materials synthesized in ionic liquid

A series of cellulose graft poly(ethylene glycol) (cellulose-graft-PEG) copolymers as phase change materials (PCMs) were synthesized in ionic liquid by using 4, 4-diphenylmethane diisocyanate as coupling reagent. FTIR and ¹H NMR characterized the structure of the copolymers. Differential scanning calorimetry (DSC) indicated that the copolymers showed phase transitions with large thermal storage density, and the phase change temperature is in the range of 40-60 °C. The transition temperature and enthalpy can be tailored by changing the molecular weight and the content of poly(ethylene glycol) (PEG) side chains. The copolymers are solid-solid PCMs with good thermal stability. Expanded graphite (EG) with 2, 5 and 10 wt% was added to the PCMs to improve the thermal conductivity. It was found that the thermal conductivity enhanced significantly with increasing EG content. The cellulose-graft-PEG/EG composite PCMs have potential applications in thermal energy storage and temperature control.     

Preparation and characterization of flame retardant form-stable phase change materials composed by EPDM,paraffin and nano magnesium hydroxide

Paraffin, one of the important thermal energy storage materials, possesses various desirable characteristics (e.g. high heat of fusion, variable phase change temperature, self-nucleating, no phase segregation and low cost), but has low thermal stability and is flammable. In the current study, form-stable phase change materials (PCMs) based on EPDM (supported material), paraffin (dispersed phase change material), nano structured magnesium hydroxide (nano-MH) and red phosphorus (RP) with various compositions were prepared. The self-synthesized nano-MH has a kind of lamellar structure with good dispersal as characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The constructional morphology, thermal stability, latent heat and flame retardant properties of as-prepared form-stable PCM blends were evaluated by using a scanning electron microscope (SEM), thermogravimetric analysis (TGA), a differential scanning calorimeter (DSC) and limited oxygen index (LOI) tester, respectively. The SEM and DSC results show that addition of nano-MH and RP has no apparent negative effect on EPDM/paraffin three dimensional netted structures and latent heat. The TGA curves indicate that inducing the nano-MH into the form-stable PCM blends leads to the reinforcement of thermal stability, increasing the amount of char residuals at 700 °C thereby improving the flame retarding performance.     

Study on preparation and thermal properties of binary fatty acid/diatomite shape-stabilized phase change materials

The choice of fatty acids as shape-stabilized phase change materials (PCMs) will increase the feasibilities of PCMs in practical applications due to the low price of the fatty acids. Compounding different fatty acids for each other is an effective way to obtain a PCM with a suitable phase-transition temperature. In this study, a series of binary fatty acids composed by capric acid, lauric acid, palmitic acid and stearic acid for each other were prepared using the phase diagram thermal dynamics calculation method. Then these binary fatty acids are absorbed in four kinds of diatomites with different specific areas, which act as a supporting material, to prepare shape-stabilized PCMs. The prepared shape-stabilized PCMs are characterized by the Scanning electron microscope (SEM) and the differential scanning calorimetry (DSC) analysis method. The results show that there is an optimum absorption ratio between binary fatty acids and the diatomite. The latent heat of capric-lauric acid/diatomite decreases to 57% of that of capric-lauric acid, and the phase-transition temperature rises from 16.36 to 16.74 °C when the capric-lauric acid is absorbed in the diatomite. The prepared capric-lauric acid/diatomite composite PCM has proper melting temperatures and latent heat for thermal energy storage application in buildings.     

Synthesis and thermal energy storage properties of ethylene dilauroyl, dimyristoyl, and dipalmitoyl amides as novel solid-liquid phase change materials

Ethylene dilauroyl, dimyristoyl, and dipalmitoyl amides were synthesized as novel solid-liquid phase change materials (PCMs) via condensation of ethylene diamine with the respective carboxyl chlorides (lauroyl chloride, myristoyl chloride, and palmytoyl chloride). The synthesized ethylene dilauroyl amide (EDLA), ethylene dimyristoyl amide (EDMA), and ethylene dipalmytoyl amide (EDPA) were characterized structurally by FT-IR and ¹H NMR spectroscopy techniques. Latent heats of melting and freezing determined using DSC technique were found to be 127.83 and −118.30 J/g for EDLA, 129.95 and −132.40 J/g for EDMA, and 150.66 and −145.22 J/g for EDPA, respectively. Phase change temperatures of these PCMs were ranged between 38.5 and 52.5 °C. The synthesized PCMs were tested for durability by accelerated thermal cyclings including 1000 melting/freezing cycles. Besides the thermal endurance of the PCMs were determined by TG analysis. Based on the results it was concluded that EDLA, EDMA, and EDPA compounds synthesized as novel solid-liquid PCMs have considerable amount of thermal energy storage potential in terms of suitable phase change temperatures, high latent heats, thermal reliability, and thermal stability. Moreover, the other advantages of the synthesized PCMs over the fatty acids used are better odor, low corrosivity, and low sublimation rates.     

Study on preparation and thermal property of binary fatty acid and the binary fatty acids/diatomite composite phase change materials

This study prepared a series of binary phase change materials by mixing decanoic acid, dodecanoic acid, hexadecanoic acid and octadecanoic acid each other. The phase-transition temperature of binary fatty acid and its corresponding mixing proportion are calculated with phase diagram thermodynamic method. The results are verified by the experimental result of the heat absorption curve and the Differential Scanning Calorimetry (DSC) analysis curve. The results show that the calculation method of phase diagram thermodynamic calculation can be taken as a basis for mixing proportion of binary fatty acid phase change materials. In addition, the decanoic–dodecanoic acid/diatomite composite phase change material (PCM) are prepared and its microstructure, thermal property and thermal reliability are characterized. The result shows that the decanoic–dodecanoic acid is uniformly adsorbed into diatomite and the form-stable PCM are formed. The phase-transition temperature and the latent heat of the decanoic–dodecanoic acid/diatomite composite PCMs is 16.74 °C and 66.8114 J/g, respectively.     

Numerical study on thermal energy storage performance of phase change material under non-steady-state inlet boundary

Due to the solar radiation intensity variation over time, the outlet temperature or mass flow rate of heat transfer fluid (HTF) presents non-steady-state characteristics for solar collector. So, in the phase change thermal energy storage (PCTES) unit which is connected to solar collector, the phase change process occurs under the non-steady-state inlet boundary condition. In present paper, regarding the non-steady-state boundary, based on enthalpy method, a two dimensional physical and mathematical model for a shell-and-tube PCTES unit was established and the simulation code was self-developed. The effects of the non-steady-state inlet condition of HTF on the thermal performance of the PCTES unit were numerically analyzed. The results show that when the average HTF inlet temperature in an hour is fixed at a constant value, the melting time (time required for PCM completely melting) decreases with the increase of initial inlet temperature. When the initial inlet temperature increases from 30 °C to 90 °C, the melting time will decrease from 42.75 min to 20.58 min. However, the total TES capacity in an hour reduces from 338.9 kJ/kg to 211.5 kJ/kg. When the average inlet mass flow rate in an hour is fixed at a constant value, with the initial HTF inlet mass flow rate increasing, the melting time of PCM decreases. The initial inlet mass flow rate increasing from 2.0 × 10⁻⁴ kg/s to 8.0 × 10⁻⁴ kg/s will lead to the melting time decreasing from 37.42 min to 23.75 min and the TES capacity of PCM increasing from 265.8 kJ/kg to 273.8 kJ/kg. Under all the studied cases, the heat flux on the tube surface increases at first, until it reaches a maximum then it decreases over time. And the larger the initial inlet temperature or mass flow rate, the earlier the maximum value appearance and the larger the maximum value.     

Study on preparation,structure and thermal energy storage property of capric–palmitic acid/attapulgite composite phase change materials

Fatty acid phase change materials (PCMs) have some advantages such as less corrosivity, no separation of subcooling phase and low price. In this paper, capric acid and palmitic acid are composited according to a certain mass ratio to prepare binary fatty acid. Capric–palmitic acid are absorbed into attapulgite by vacuum method to prepare capric–palmitic acid/attapulgite composite PCMs. Analysis methods such as differential scanning analysis (DSC), scanning electron microscope (SEM), Fourier transform infrared (FT-IR) and specific surface analysis (BET method) are used to test the thermal properties, structure and composition of the prepared composite PCM. The results indicate that the pore structure of the caplic–paltimic acid/attapulgite composite PCM is open-ended tubular capillary, which is beneficial to the adsorption. Capric acid and palmitic acid can be absorbed uniformly into attapulgite and the optimum absorption ratio of capric–palmitic binary fatty acid is 35%. There is no chemical reaction between the capric–palmitic acid and attapulgite. The phase change temperature of the capric–palmitic acid/attapulgite composite PCM is 21.71 °C and the latent heat is 48.2 J/g.     

Numerical analysis on the thermal characteristics of photovoltaic module with ambient temperature variation

A silicon photovoltaic module converts sunlight energy into electricity applying the photovoltaic effect of the semiconductor. But the performance of PV module is affected by ambient temperature. It is well known that the power and efficiency of PV module usually falls at a rate of ∼0.5%/°C and ∼0.05%/°C, respectively as increase of ambient temperature. In this study, the thermal characteristics of a PV module by change of ambient temperature from −25 °C in minimum to 50 °C in maximum is investigated through a thermal analysis simulation program. In the end, a simulation method to attach fins to the backside of PV module is discussed. This work shows the comparison of the thermal characteristics between a PV module with and without fins.     

Thermal aspects of c-Si photovoltaic module energy rating

Standard test conditions (STC) of photovoltaic (PV) modules are not representative of field conditions; PV module operating temperature often rises up to 30 °C above STC temperature (25 °C), causing a performance drop of 0.5%/°C for crystalline silicium modules. Normal operating cell temperature (NOCT) provides better estimates of PV module temperature rise. It has nevertheless to be measured; moreover NOCT wind speed conditions do not always fit field conditions. The purpose of this work is to model average PV module temperature at given irradiance levels as a function of meteorological parameters and PV module implementation. Thus, no empirical knowledge of PV module thermal behaviour is required for energy rating basing on irradiation distributions over irradiance levels.     

Platinum/tin oxide/carbon cathode catalyst for high temperature PEM fuel cell

The performance of high temperature polymer electrolyte fuel cell (HT-PEMFC) using platinum supported over tin oxide and Vulcan carbon (Pt/SnOx/C) as cathode catalyst was evaluated at 160-200 °C and compared with Pt/C. This paper reports first time the Pt/SnOx/C preparation, fuel cell performance, and durability test up to 200 h. Pt/SnOx/C of varying SnO compositions were characterized using XRD, SEM, TEM, EDX and EIS. The face-centered cubic structure of nanosized Pt becomes evident from XRD data. TEM and EDX measurements established that the average size of the Pt nanoparticles were ∼6 nm. Low ionic resistances were derived from EIS, which ranged from 0.5 to 5 Ω-cm² for cathode and 0.05 to 0.1 Ω-cm² for phosphoric acid, doped PBI membrane. The addition of the SnOx to Pt/C significantly promoted the catalytic activity for the oxygen reduction reaction (ORR). The 7 wt.% SnO in Pt/SnO₂/C catalyst showed the highest electro-oxidation activity for ORR. High temperature PEMFC measurements performed at 180 °C under dry gases (H₂ and O₂) showed 0.58 V at a current density of 200 mA cm⁻², while only 0.40 V was obtained in the case of Pt/C catalyst. When the catalyst contained higher concentrations of tin oxide, the performance decreased as a result of mass transport limitations within the electrode. Durability tests showed that Pt/SnOx/C catalysts prepared in this work were stable under fuel cell working conditions, during 200 h at 180 °C demonstrate as potential cathode catalyst for HT-PEMFCs.     

Design and experimental testing of the performance of an outdoor LiBr/H2O solar thermal absorption cooling system with a cold store

A domestic-scale prototype experimental solar cooling system has been developed based on a LiBr/H₂O absorption system and tested during the 2007 summer and autumn months in Cardiff University, UK. The system consisted of a 12 m² vacuum tube solar collector, a 4.5 kW LiBr/H₂O absorption chiller, a 1000 l cold storage tank and a 6 kW fan coil. The system performance, as well as the performances of the individual components in the system, were evaluated based on the physical measurements of the daily solar radiation, ambient temperature, inlet and outlet fluid temperatures, mass flow rates and electrical consumption by component. The average coefficient of thermal performance (COP) of the system was 0.58, based on the thermal cooling power output per unit of available thermal solar energy from the 12 m² Thermomax DF100 vacuum tube collector on a hot sunny day with average peak insolation of 800 W/m² (between 11 and 13.30 h) and ambient temperature of 24 °C. The system produced an electrical COP of 3.6. Experimental results prove the feasibility of the new concept of cold store at this scale, with chilled water temperatures as low as 7.4 °C, demonstrating its potential use in cooling domestic scale buildings.