Polyethylene Glycol/Rice Husk Ash Shape-Stabilized Phase Change Materials: Recovery of Thermal Energy Storage Efficacy via Engineering Porous Support Structure.

This study focuses on modifying the porous structure of acid-treated rice husk ash (ARHA) to enhance the thermal energy storage capacity of poly(ethylene glycol) (PEG) confined within shape-stabilized phase change materials. The modification process involved a cost-effective sol-gel method in which ARHA was initially dissolved in an alkaline solution and subsequently precipitated in an acidic environment. ARHA, being a mesoporous SiO2-based material with a high surface area but low pore volume, had limited capacity to adsorb PEG (50%). Furthermore, it hindered the crystallinity of impregnated PEG by fostering abundant interfacial hydrogen bonds (H-bonds), resulting in a diminished thermal energy storage efficiency. Following modification of the porous structure, the resulting material, termed mARHA, featured a three-dimensional macroporous network, providing ample space to stabilize a significant amount of PEG (70%) without any leakage. Notably, mARHA, with a reduced surface area, effectively mitigated interfacial H-bonds, consequently enhancing the crystallinity of impregnated PEG. This modification led to the recovery of thermal energy storage efficacy from 0 J/g for PEG/ARHA to 109.3 J/g for PEG/mARHA. Additionally, the PEG/mARHA composite displayed improved thermal conductivity, reliable thermal performance, and effective thermal management when used as construction materials. This work introduces a straightforward and economical strategy for revitalizing thermal energy storage in PEG composites confined within RHA-based porous supports, offering promising prospects for large-scale applications in building energy conservation.

Using Carbonized Cotton Fabric Waste to Prepare Poly(ethylene glycol) Composite Phase Change Materials with Improved Thermal Conductivity and Solar-to-Thermal Conversion.

Poly(ethylene glycol) (PEG) boasts excellent thermal energy storage capabilities but lacks efficiency in thermal conductivity and solar absorption. Simultaneously, the escalating concern surrounding the substantial volume of discarded cotton fabric underscores environmental issues. In this study, we devised composite phase change materials (PCMs) by embedding PEG into a carbon cotton material (CCM), varying PEG content from 50 to 80%, and conducted a comprehensive analysis of their thermal properties and solar-to-thermal conversion. The CCM, crafted from a waste 100% cotton towel through carbonization, provided an optimal porous structure that accommodated a significant 70% PEG content without any leakage, thanks to interactions such as surface tension, capillary forces, and interfacial hydrogen bonds. These PEG/CCM composites exhibited impressive crystallization fractions (>92%), resulting in notable thermal energy storage capacities ranging from 85.3 to 143.2 J/g as the PEG content increased from 50 to 80%. Moreover, these composites showed high thermal stability and exceptional cycling durability even after 500 melting/crystallization cycles. Notably, their thermal conductivities markedly increased to a range of 0.46-0.85 W/m·K compared to pure PEG's modest 0.24 W/m·K. Furthermore, the PEG/CCM composites substantially augmented visible and near-infrared (VIS-NIR) light absorption. Evaluation of solar-to-thermal conversion illustrated the composite's ability to efficiently convert solar energy into thermal energy, storing and subsequently releasing it through melting and crystallization processes. This study introduces a novel class of composite PCMs characterized by cost-effectiveness, outstanding thermal performance, and impressive solar-to-thermal conversion capabilities. These composite PCMs hold significant promise for large-scale solar-to-thermal energy storage applications while contributing to the sustainability of cotton waste management.

Polyethylene Glycol Confined in SiO2-Modified Expanded Graphite as Novel Form-Stable Phase Change Materials for Thermal Energy Storage.

Form-stable phase change materials (FSPCMs) composed of poly(ethylene glycol) (PEG) encapsulated in SiO2-modified expanded graphite (EG@SiO2) were prepared and investigated for thermal energy storage behaviors. The modification of SiO2 on EG was done using a simple sol-gel method, and then the resulting EG@SiO2 was introduced to confine PEG at varying content (60-90 wt %). Surface properties (including microstructure, morphology, and functional groups), PEG adsorptivity, leakage-proof ability, and thermal energy storage of the prepared materials were thoroughly characterized and discussed. The EG@SiO2 with 15 wt % SiO2 outstandingly adsorbed PEG as compared to the pristine EG, showing up >80 wt % of PEG. As a result, PEG was well stabilized in EG@SiO2 porous network without leakage, owing to capillary force, surface tension, and hydrogen bonding interactions. The optimal 80 wt % PEG/EG@SiO2 composite possessed high crystallinity (93.5%), high thermal energy storage capacity (132.5 J/g), and excellent thermal conductivity (4.086 W/m·K). In addition, it exhibited good cycling durability after 500 repeated melting/crystallization cycles. The high thermal efficacy and inexpensiveness would make the PEG/EG@SiO2 FSPCMs suitable for scale-up applications in thermal energy storage.

Enhanced Thermal Energy Storage of n-Octadecane-Impregnated Mesoporous Silica as a Novel Shape-Stabilized Phase Change Material.

A series of n-octadecane/mesoporous silica (C18/MS) shape-stabilized phase change materials (SSPCMs) with varying C18 content were prepared, and the effects of adsorbed C18 distributed within porous MS on the thermal properties were analyzed. As characterized, C18 was first infiltrated into the mesoporous space, resulting in a SSPCM with a maximum of ∼52 wt % C18. Additional adsorption of C18 occurred on the external surface of MS. Consequently, the optimum 70 wt % C18 SSPCM had no C18 leakage and exhibited a heat storage capacity of 135.6 J/g and crystallinity of 83.5%, which were much larger than those of 52 wt % C18 SSPCM (60.2 J/g and 68.2%, respectively). The prepared C18/MS SSPCMs showed excellent thermal stability and thermal reliability up to 1000 accelerated thermal cycle tests. Moreover, the C18/MS SSPCM incorporated in gypsum effectively reduced the temperature changes compared with the original gypsum, suggesting the promising application of the prepared C18/MS SSPCM for energy-saving building applications.