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In this study, beeswax-tetradecanol/expanded perlite composited with carbon fiber (BW-TD-CF/EP) composite phase change materials (CPCMs) have been prepared via vacuum impregnation method for solar energy utilization. The chemical compatibility, microstructure and thermal properties of CPCMs are characterized and measured, which proves that it is no chemical interaction among the raw materials but physical combination and BW-TD-CF is sufficiently absorbed into the EP porous structure with no leakage even in the molten state. According to differential scanning calorimeter (DSC) results, BW-TD-CF/EP composite melts at 34 °C with high enthalpy value of 178.7 kJ/kg, while thermal cycling measurements show that the form-stable composite PCM has adequate stability after being subjected to 200 melting/freezing cycles. Morever, thermal conductivity of BW-TD/EP composite is enhanced from 0.443 Wm−1 K−1 to 1.245 Wm−1 K−1 by adding CF. In result, the form-stable composite PCMs have more appropriate thermal properties and better thermal stability in building for solar energy utilization.

In this study, the effect of the introduction of carbon nanotubes (CNTs) as a filler for enhancing the thermal conductivity of paraffin-carbon nanotubes/expanded perlite form-stable composite phase change materials (PA-CNTs/EP FS-CPCMs) was experimentally investigated. Four samples of PA-CNTs/EP FS-CPCMs with different CNT mass fractions were prepared by vacuum impregnation. Scanning electron microscopy was employed to investigate the morphology and microstructure of CNTs, EP, and PA-CNTs/EP FS-CPCMs. Differential scanning calorimetry was employed to examine the thermal properties of PA-CNTs/EP FS-CPCMs, and results indicated that the latent heat and phase-change temperatures of the PA-CNTs/EP FS-CPCMs slightly change with the CNTs mass fractions. The thermal conductivity of PA-CNTs/EP FS-CPCMs5.27 (0.516 W m −1 K −1 ) was 4.82 times that of PA-CNTs/EP FS-CPCMs0. The thermal storage and release properties of PA-CNTs/EP FS-CPCMs were significantly improved as compared with those of PA-CNTs/EP FS-CPCMs0. Results obtained from Fourier transform infrared spectroscopy, thermogravimetric analysis, and thermal cycling tests showed that PA-CNTs/EP FS-CPCMs exhibit good chemical and thermal stabilities. The as-prepared PA-CNTs/EP FS-CPCMs demonstrate considerable potential as thermal energy storage materials.

In this study, the fatty acid eutectics (capric acid (CA) and lauric acid (LA) eutectics) were impregnated into the expanded perlite (EP) and expanded vermiculite (EVM) to form the two kinds of composite phase change material (PCM). The chemical structure, crystalloid phase were determined by the Fourier transformation infrared spectroscope, X-ray diffractometer. The results show that the eutectics with the EP and EVM do not undergo a chemical reaction and only undergo a physical combination. The SEM results proved that eutectics are well adsorbed in the porous structure of the EP and EVM. The thermal properties were determined by the differential scanning calorimeter (DSC). The DSC result shows that the melting temperatures and latent heat values of the PCMs are in the range of about 21–23 °C and 81–117 J/g. The maximum impregnation ratio of fatty acid eutectics into EP and EVM were 82.93% and 57.48%. The thermal cycling test proves that the composites have good thermal reliability. TG analysis revealed that the composite PCMs had high thermal durability property above their working temperature ranges. Besides, thermal conductivity of the CA-LA/EP and CA-LA/EVM was increased approximately as 89.14% and 87.41% by adding 5 wt.% expanded graphite (EG). It is envisioned that the prepared shape-stabilized PCMs have considerable potential for developing their roles in thermal energy storage system.

In this study, novel polyethylene glycol @ Si3N4 nanowires as phase-change materials (PCMs) were developed by using ultrasonic cell disruptor. The results obtained herein indicate that these nanowires can be a potential carrier for preparing PCMs. The results show that PEG is composited in a fluffy nano-network structure of Si3N4 nanowires, which could not be easily leaked from this structure for the solid–liquid phase transition. X-ray diffraction and Fourier transform infrared spectroscopy were employed for investigating the structures of PCMs; the results show that a chemical reaction does not occur between PEG and Si3N4 nanowires. Differential scanning calorimetry analysis results indicated that PCMs exhibit appropriate phase-change temperature and excellent high-phase change enthalpy. From the TGA results, PCMs exhibit perfect thermal stability. The PCMs could perfectly maintain their phase transition after 100 melting–freezing cycles. The thermal conductivity of PCMs-1 was 0.362 W/(mK), which was enhanced by 88.54% in comparison with that to pure PEG. The heat storage or release rate of PCMs is significantly more rapid than that of pure PEG for practical applications.

In this study, polyethylene glycol/expanded perlite composite with carbon layer phase-change materials were prepared. EP was impregnated with a sucrose solution, followed by carbonation in situ by the carbon-bed method, for obtaining EPC composite, thus providing an important method for enhancing the thermal conductivity of composite PCMs. Scanning electron microscopy images showed that the EPC composite with a highly porous structure composed of rough micro-pores could act as a good supporting material for absorbing molten PEG. The results obtained from differential scanning calorimeter analysis indicated that the values for the latent heat and temperature of PEPC composite during melting were 134.93 J/g and 55.19 °C, respectively, while, these values were 129.27 J/g and 46.71 °C during freezing, respectively. The thermal conductivity of PEPC composite was 0.479 W/(mK), which was 2.975 times that of PEP composite. The results obtained from Fourier transform infrared spectroscopy and thermo-gravimetric analysis showed that PEPC composite exhibited good chemical stability and thermal stability, respectively. Furthermore, thermal cycling tests indicated that PEPC composite exhibited good thermal reliability after 200 melting/freezing cycles. In conclusion, PEPC composite with excellent thermal properties, ideal thermal conductivity, good thermal reliability and chemical stability could act as the promising building filler materials for the sustainable development of energy-efficient buildings.

In this work, the mechanical properties and solid particle erosion wear behavior of LaMgAl11O19–Al2O3 ceramics toughened and reinforced with LaMgAl11O19 platelets were investigated. The effects of LaMgAl11O19 additions, impingement angles (30°, 45°, 60°, 75°, and 90°), and erosion temperatures varying from room temperature to 1400°C on the erosion rates and material removal mechanisms of LaMgAl11O19–Al2O3 composites were systematically studied. The results indicated that LaMgAl11O19–Al2O3 ceramics exhibited superior erosive wear resistance compared to monolithic Al2O3 ceramics at room and elevated temperatures due to their enhanced mechanical properties and improved microstructure resulting from the introduction of an appropriate amount of LaMgAl11O19 platelets. Examination of the eroded surfaces of LaMgAl11O19–Al2O3 composites revealed that erosion temperatures and impingement angles play important roles in determining the erosion behavior and mechanisms of the tested materials. For the case of elevated temperature and oblique erosion, plowing and subsurface intergranular fracture are the predominant mechanisms resulting in material removal, whereas at room temperature and normal impact, the erosion process of the targets is primarily dominated by grain ejection and lateral crack intersection.

Lauric acid(LA)/expanded vermiculite (EVM) form-stable phase change materials were synthesized via vacuum impregnation method. In the composites, lauric acid was utilized as a thermal energy storage material and the expanded vermiculite behaved as the supporting material. XRD and FT-IR results demonstrate that lauric acid and expanded vermiculite in the composite do not undergo a chemical reaction and only undergo a physical combination. Microstructural analysis indicates that lauric acid is sufficiently absorbed in the expanded vermiculite porous network, while displaying negligible leakage even under the molten state. According to DSC results, the 70 wt.% LA/EVM sample melts at 41.88 °C with a latent heat of 126.8 J/g and solidifies at 39.89 °C with a latent heat of 125.6 J/g. Thermal cycling measurements show that the form-stable composite PCM has adequate stability even after being subjected to 200 melting/freezing cycles. Furthermore, the thermal conductivity of the composite PCM increased by approximately 78% with the addition of 10 wt.% expanded graphite (EG). Thus, the form-stable composite PCM is a suitable option for thermal energy storage for building and solar heating system applications.

Novel form-stable composite phase change materials (FS-CPCMs) of polyethylene glycol (PEG)/Cu/SiO2 were prepared by adding Cu powder to PEG and SiO2 via the ultrasound-assisted sol–gel method. This method ensured the uniform distribution of Cu powder in the FS-CPCMs, thus providing an important method to develop composite phase change materials (CPCMs) with a high thermal conductivity. The FS-CPCMs were characterized by various techniques. The results showed that the FS-CPCMs remained in the solid state without leakage above the melting point of PEG. The XRD and FTIR results indicated that no new chemical bond was formed between the constituents of FS-CPCMs: Cu, PEG, and SiO2. The DSC and TGA analyses showed that the FS-CPCMs had an optimum phase-change temperature, a high enthalpy of phase change, an excellent thermal stability, and a good form-stable performance. The thermal conductivity was 0.431 W m−1 K−1 for 3.45 wt% Cu powder in the FS-CPCMs, an increase of 49.13% compared to pure PEG.

Carbon foam/expanded graphite composite (CEC) was prepared from a sucrose-expandable graphite resin using a thermal foaming method. This CEC was impregnated through its pores with paraffin to obtain a paraffin/carbon foam/expanded graphite composite (PCEC). In the case of CECs, when the amount of added expandable graphite reached 10 wt% to 15 wt%, the microstructure of the CEC was damaged because of the expansion in volume of the expandable graphite. Fourier transform infra-red spectroscopy and X-ray diffraction analysis of PCECs showed that there was no chemical interaction between the paraffin and CECs. With an increase in the amount of expandable graphite in CECs, the adsorption capacity of paraffin and the latent heat first showed an increase and then decreased. The heat transfer capability of the paraffin was truly improved by the CECs. The processes for the preparation of the CECs and PCECs were environmentally friendly, convenient, and inexpensive. The PCECs, with good thermal properties and chemical stabilities, are suitable for low temperature (40–50 °C) thermal energy storage applications.

Sialon–ZrN powders were synthesized from low-grade bauxite using a zirconite additive by carbothermal reduction nitridation (CRN). The as-synthesized Sialon–ZrN powders were subsequently used as SiC-based free-fired refractories. Their phase compositions and microstructures of the powders were determined using X-ray diffraction and scanning electron microscopy. The physical properties and blast furnace (BF) slag resistance of the SiC–Sialon–ZrN free-fired refractories were also studied. The results show that the low-grade bauxite and zirconite powders were transformed to β-Sialon and ZrN by the CRN process at 1600 °C. The phenolic resin provided a strongly bonded interface between the Sialon–ZrN matrix and SiC particles and thus enhanced their combined strength after drying at 150 °C. The strength increased as the temperature was elevated from 1000 °C to 1500 °C. As the ZrN content increased, the slag erosion rate of the SiC–Sialon–ZrN free-fired refractories initially decreased and then increased after being heated at 1500 °C. The presence of ZrO 2 in the slag (oxidized from ZrN) revealed that the ZrO 2 did not react with other oxides in the BF slag to form low melting point phases. This may play a crucial role in its BF slag erosion resistance. The corrosion mechanism of the BF slag towards the as-prepared SiC–Sialon–ZrN free-fired refractories was determined to be oxidation-erosion-dissolution-penetration.

Nanostructure reinforced nitride ceramics play an important role in the family of structural ceramics. In this study, large scale of one-dimensional (1D) β-sialon nanostructures and β-sialon-β-Si3N4 composite powders were synthesized simultaneously via a reduction nitridation process by using powders of silicon, aluminum, and silica as raw materials. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM/HRTEM), Fourier-transform infrared spectroscopy (FT-IR) and energy dispersive x-ray spectroscopy (EDS) were used to characterize the phase composition, morphology, and microstructure of the as-obtained products. As a result, large scale of 1D β-sialon nanostructures can be prepared at 1600 °C. The diameter of the as-prepared nanowires in the range of 80 to 170 nm can be tailored by the addition of aluminum. The growth of 1D β-sialon nanostructures is achieved by a vapor-solid (VS) mechanism. Photoluminescence (PL) of the 1D β-sialon nanostructures was characterized which exhibit violet/blue emission peaks, making it have the potential to be applied in optoelectronic nanodevices. Besides, nitride ceramic composite powders including β-Si3N4 and β-sialon with in situ formed β-sialon nanowires were also achieved. The phase transformation behavior and the thermodynamical analysis of the ceramic composite powders were also studied by characterizing the phase composition of the products synthesized at different temperature. The as-grown β-sialon nanowires and the composite powders have great potential to be applied in nanostructure reinforced structural ceramics.

Radial mesoporous silica (RMS) sphere was tailor-made for further applications in producing shape-stabilized composite phase change materials (ss-CPCMs) through a facile self-assembly process using CTAB as the main template and TEOS as SiO2 precursor. Novel ss-CPCMs composed of polyethylene glycol (PEG) and RMS were prepared through vacuum impregnating method. Various techniques were employed to characterize the structural and thermal properties of the ss-CPCMs. The DSC results indicated that the PEG/RMS ss-CPCM was a promising candidate for building thermal energy storage applications due to its large latent heat, suitable phase change temperature, good thermal reliability, as well as the excellent chemical compatibility and thermal stability. Importantly, the possible formation mechanisms of both RMS sphere and PEG/RMS composite have also been proposed. The results also indicated that the properties of the PEG/RMS ss-CPCMs are influenced by the adsorption limitation of the PEG molecule from RMS sphere with mesoporous structure and the effect of RMS, as the impurities, on the perfect crystallization of PEG.