Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption

Composites ‘salt in porous matrix’ has been considered as a promising candidate for thermal energy storage due to their large sorption capacity, energy density and high cyclic stability. In this study, novel salt composites were prepared by using different mesoporous silica with large pore size and...

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Main Authors: Xin Liu, Haomin Wang, Xiao Liu, Fangming Yang, Li Guan, Suleiman Sani, Chenggong Sun, Yupeng Wu
Format: Article
Language:English
Published: Elsevier 2022-11-01
Series:Energy Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352484722006928
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author Xin Liu
Haomin Wang
Xiao Liu
Fangming Yang
Li Guan
Suleiman Sani
Chenggong Sun
Yupeng Wu
author_facet Xin Liu
Haomin Wang
Xiao Liu
Fangming Yang
Li Guan
Suleiman Sani
Chenggong Sun
Yupeng Wu
author_sort Xin Liu
collection DOAJ
description Composites ‘salt in porous matrix’ has been considered as a promising candidate for thermal energy storage due to their large sorption capacity, energy density and high cyclic stability. In this study, novel salt composites were prepared by using different mesoporous silica with large pore size and pore volume as the porous matrices and MgSO4 via impregnation method. The results demonstrated that both MgSO4 loading level and textural properties of the porous matrices played a critical role in determining tha vapour pressure ofe water adsorption performance of salt composites. Tested at 30 °C and a vapour pressure of 25 mbar, salt composites prepared by using mesostructured cellular foam (MCF) with 3D-interconnected porous structure exhibited excellent water adsorption capacity of 50 wt% at MgSO4 loading level of 50 wt%, which was much higher than that of commercial PQ Silica. Further characterization showed that the 3D-interconnected porous structure and large pore size of MCF benefited the dispersion of salt and the reduced diffusion resistance of vapour flux inside the pores, which could effectively improve the water adsorption capacity and hydration/dehydration rate of salt composites. All the results indicated that the novel composites are expected to be a promising candidate for low temperature energy storage.
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spelling doaj.art-8c8390041f1e4d449e156401531d02542023-04-18T09:27:45ZengElsevierEnergy Reports2352-48472022-11-01849134921Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorptionXin Liu0Haomin Wang1Xiao Liu2Fangming Yang3Li Guan4Suleiman Sani5Chenggong Sun6Yupeng Wu7Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UK; School of Energy and Power Engineering, Shandong University, Jinan, PR ChinaFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKFaculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UK; Corresponding author.Composites ‘salt in porous matrix’ has been considered as a promising candidate for thermal energy storage due to their large sorption capacity, energy density and high cyclic stability. In this study, novel salt composites were prepared by using different mesoporous silica with large pore size and pore volume as the porous matrices and MgSO4 via impregnation method. The results demonstrated that both MgSO4 loading level and textural properties of the porous matrices played a critical role in determining tha vapour pressure ofe water adsorption performance of salt composites. Tested at 30 °C and a vapour pressure of 25 mbar, salt composites prepared by using mesostructured cellular foam (MCF) with 3D-interconnected porous structure exhibited excellent water adsorption capacity of 50 wt% at MgSO4 loading level of 50 wt%, which was much higher than that of commercial PQ Silica. Further characterization showed that the 3D-interconnected porous structure and large pore size of MCF benefited the dispersion of salt and the reduced diffusion resistance of vapour flux inside the pores, which could effectively improve the water adsorption capacity and hydration/dehydration rate of salt composites. All the results indicated that the novel composites are expected to be a promising candidate for low temperature energy storage.http://www.sciencedirect.com/science/article/pii/S2352484722006928Composite materialsMagnesium sulphateMesoporous silicaThermochemical energy storage
spellingShingle Xin Liu
Haomin Wang
Xiao Liu
Fangming Yang
Li Guan
Suleiman Sani
Chenggong Sun
Yupeng Wu
Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
Energy Reports
Composite materials
Magnesium sulphate
Mesoporous silica
Thermochemical energy storage
title Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
title_full Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
title_fullStr Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
title_full_unstemmed Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
title_short Development of MgSO4/mesoporous silica composites for thermochemical energy storage: the role of porous structure on water adsorption
title_sort development of mgso4 mesoporous silica composites for thermochemical energy storage the role of porous structure on water adsorption
topic Composite materials
Magnesium sulphate
Mesoporous silica
Thermochemical energy storage
url http://www.sciencedirect.com/science/article/pii/S2352484722006928
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