CaO/H2O Thermochemical Heat Storage Capacity of a CaO/CeO2 Composite from CO2 Capture Cycles

2020 ◽  
Vol 59 (38) ◽  
pp. 16741-16750
Author(s):  
Zhiguo Bian ◽  
Yingjie Li ◽  
Chaoying Sun ◽  
Chunxiao Zhang ◽  
Zeyan Wang ◽  
...  
2018 ◽  
Vol 320 ◽  
pp. 316-324 ◽  
Author(s):  
Ntuthuko W. Hlongwa ◽  
Daniel Sastre ◽  
Emmanuel Iwuoha ◽  
Alfonso J. Carrillo ◽  
Chinwe Ikpo ◽  
...  

2019 ◽  
Vol 108 ◽  
pp. 02013
Author(s):  
Piotr Babiński ◽  
Michalina Kotyczka – Morańska ◽  
Jarosław Zuwała

The paper presents the results of the fundamental research devoted to the application of MgSO4 as a heat carrier for thermochemical seasonal storage system devoted for household application followed by the results of 35kWh storage tank (TRL IV) charging and discharging tests. Seasonal thermochemical heat storage, based on the reversible reactions of hydratation and dehydratation of a solid medium gives an opportunity to accumulate the energy with a storage capacity exceeding 300-400 kWh/m3.


2018 ◽  
Vol 174 ◽  
pp. 8-19 ◽  
Author(s):  
Yi Yuan ◽  
Yingjie Li ◽  
Lunbo Duan ◽  
Hantao Liu ◽  
Jianli Zhao ◽  
...  

2021 ◽  
Vol 11 (2) ◽  
pp. 682
Author(s):  
Gabriele Seitz ◽  
Farid Mohammadi ◽  
Holger Class

Calcium oxide/Calcium hydroxide can be utilized as a reaction system for thermochemical heat storage. It features a high storage capacity, is cheap, and does not involve major environmental concerns. Operationally, different fixed-bed reactor concepts can be distinguished; direct reactor are characterized by gas flow through the reactive bulk material, while in indirect reactors, the heat-carrying gas flow is separated from the bulk material. This study puts a focus on the indirectly operated fixed-bed reactor setup. The fluxes of the reaction fluid and the heat-carrying flow are decoupled in order to overcome limitations due to heat conduction in the reactive bulk material. The fixed bed represents a porous medium where Darcy-type flow conditions can be assumed. Here, a numerical model for such a reactor concept is presented, which has been implemented in the software DuMux. An attempt to calibrate and validate it with experimental results from the literature is discussed in detail. This allows for the identification of a deficient insulation of the experimental setup. Accordingly, heat-loss mechanisms are included in the model. However, it can be shown that heat losses alone are not sufficient to explain the experimental results. It is evident that another effect plays a role here. Using Bayesian inference, this effect is identified as the reaction rate decreasing with progressing conversion of reactive material. The calibrated model reveals that more heat is lost over the reactor surface than transported in the heat transfer channel, which causes a considerable speed-up of the discharge reaction. An observed deceleration of the reaction rate at progressed conversion is attributed to the presence of agglomerates of the bulk material in the fixed bed. This retardation is represented phenomenologically by mofifying the reaction kinetics. After the calibration, the model is validated with a second set of experimental results. To speed up the calculations for the calibration, the numerical model is replaced by a surrogate model based on Polynomial Chaos Expansion and Principal Component Analysis.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ata Ur Rehman ◽  
Muhammad Zahir Shah ◽  
Shehla Rasheed ◽  
Wasim Afzal ◽  
Muhammad Arsalan ◽  
...  

Abstract Salt hydrates (MgSO4 and ZnSO4) impregnated in zeolites, offer a variety of improvements, mostly providing a large surface area for salt hydrates and water molecules. A composite of 5 and 10% of salt contents were prepared as heat storage materials. The study’s finding showed that dehydration enthalpy of MgSO4 (1817 J g−1) and ZnSO4 (1586 J g−1) were 10 and 15% improved than pure salt hydrates by making composites. During the hydration process of composites, the water sorption is 30–37% improved and further the increasing of salt contents in composites enhances more 10% increase in the water resorption. The cyclicability of MgSO4/zeolite and ZnSO4/zeolite were 45 and 51% improved than their corresponding pure salt hydrates. The effect of humidity on the water sorption result reveals that composites of MgSO4/zeolite and ZnSO4/zeolite at 75% relative humidity (RH), the mass of water are 51 and 40% increase than 55% RH.


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