scholarly journals Synthesis of Mesoporous γ-Alumina Support for Water Composite Sorbents for Low Temperature Sorption Heat Storage

Energies ◽  
2021 ◽  
Vol 14 (22) ◽  
pp. 7809
Author(s):  
Manca Ocvirk ◽  
Alenka Ristić ◽  
Nataša Zabukovec Logar

The efficiency of thermochemical heat storage is crucially determined by the performance of the sorbent used, which includes a high sorption capacity and a low regeneration temperature. The thermochemical salt hydrate– γ-alumina composite sorbents are promising materials for this application but lack systematic study of the influence of γ-alumina structural properties on the final storage performance. In this study, mesoporous γ-Al2O3 supports were prepared by solvothermal and hydrothermal synthesis containing a block copolymer (F-127) surfactant to design thermochemical CaCl2 and LiCl composite water sorbents. Altering the solvent in the synthesis has a significant effect on the structural properties of the γ-Al2O3 mesostructure, which was monitored by powder XRD, nitrogen physisorption, and SEM. Solvothermal synthesis led to a formation of mesoporous γ-Al2O3 with higher specific surface area (213 m2/g) and pore volume (0.542 g/cm3) than hydrothermal synthesis (147 m2/g; 0.414 g/cm3). The highest maximal water sorption capacity (2.87 g/g) and heat storage density (5.17 GJ/m3) was determined for W-46-LiCl containing 15 wt% LiCl for space heating, while the best storage performance in the sense of fast kinetics of sorption, without sorption hysteresis, low desorption temperature, very good cycling stability, and energy storage density of 1.26 GJ/m3 was achieved by W-46-CaCl2.

Nanomaterials ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 27 ◽  
Author(s):  
Alenka Ristić ◽  
Nataša Zabukovec Logar

Sorption heat storage, as one of low-energy consuming technologies, is an approach to reduce CO2 emissions. The efficiency of such technology is governed by the performance of the applied sorbents. Thus, sorbents with high water sorption capacity and regeneration temperature from 80 to 150 °C are required. Incorporation of hygroscopic salt such as calcium chloride into porous materials is a logical strategy for increasing the water sorption capacity. This work reports the study on the development of composites with PHTS (plugged hexagonal templated silicate) matrix with an average pore size of 5.7 nm and different amounts of calcium chloride (4, 10, 20 wt.%) for solar thermal energy storage. These composites were prepared by wetness incipient impregnation method. Structural properties were determined by X-ray diffraction (XRD), nitrogen physisorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). CaCl2 was confined in micro- and mesopores of the matrix. The resulting CaCl2-PHTS materials were used for water sorption at 40 °C, showing an increase of maximal water uptake with higher amount of calcium chloride from 0.78 g/g to 2.44 g/g of the dry composite. A small reduction in water uptake was observed after 20 cycles of sorption/desorption between temperatures of 140 °C and 40 °C, indicating good cycling stability of these composites under the working conditions.


Molecules ◽  
2020 ◽  
Vol 25 (5) ◽  
pp. 1249 ◽  
Author(s):  
Ecaterina Stela Dragan ◽  
Doina Humelnicu

Removal of Cr(VI) from the environment represents a stringent issue because of its tremendous effects on living organisms. In this context, design of sorbents with high sorption capacity for Cr(VI) is getting a strong need. For this purpose, poly(vinylbenzyl chloride), impregnated into porous silica (PSi), was cross-linked with either N,N,N’,N’-tetramethyl-1,2-ethylenediamine (TEMED) or N,N,N’,N’-tetramethyl-1,3-propanediamine, followed by the reaction of the free -CH2Cl groups with N,N-diethyl-2-hydroxyethylamine to generate strong base anion exchangers (ANEX) inside the pores. The PSi/ANEX composite sorbents were deeply characterized by FTIR spectroscopy, SEM-energy dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), and water uptake. The sorption performances of composites against Cr(VI) were investigated as a function of pH, contact time, initial concentration of Cr(VI), and temperature. It was found that the cross-linker structure and the silica morphology are the key factors controlling the sorption capacity. The adsorption process was spontaneous and endothermic and well described by pseudo-second-order kinetic and Sips isotherm models. The maximum sorption capacity of 311.2 mg Cr(VI)/g sorbent was found for the composite prepared with mesoporous silica using TEMED as cross-linker. The PSi/ANEX composite sorbents represent an excellent alternative for the removal of Cr(VI) oxyanions, being endowed with fast kinetics, equilibrium in about 60 min, and a high level of reusability in successive sorption/desorption cycles.


2014 ◽  
Vol 536-537 ◽  
pp. 1477-1480 ◽  
Author(s):  
Dong Dong Wu ◽  
Hua Wang ◽  
Yong Gang Wei ◽  
Kong Zhai Li

Aluminum is supposed to be admirable phase change materials (PCMs) for thermal energy storage due to its excellent heat storage density and thermal conductivity. However, its application is limited because of the flowability and corrosivity when it melt. The Al/AlN-Al2O3composite PCMs with stable thermal energy storage performance were prepared by direct nitridation method. The research showed that nitridation temperature and nitridation time are key parameters of heat storage performance of the composite materials. The morphology and thermal energy storage performance and components of the Al/AlN-Al2O3composite PCMs were investigated by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), X-ray diffraction (XRD). The results showed that the tiny particles of aluminum powders were closely coated by AlN-Al2O3encapsulating materials. This structure can prevent the flowability of the liquid aluminum and also can avoid environmental impact when the it melt, meanwhile , the composite PCMs have the performance such as stability, high thermal storage density.


Energies ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3006
Author(s):  
Serge Nyallang Nyamsi ◽  
Ivan Tolj

Two-tank metal hydride pairs have gained tremendous interest in thermal energy storage systems for concentrating solar power plants or industrial waste heat recovery. Generally, the system’s performance depends on selecting and matching the metal hydride pairs and the thermal management adopted. In this study, the 2D mathematical modeling used to investigate the heat storage system’s performance under different thermal management techniques, including active and passive heat transfer techniques, is analyzed and discussed in detail. The change in the energy storage density, the specific power output, and the energy storage efficiency is studied under different heat transfer measures applied to the two tanks. The results showed that there is a trade-off between the energy storage density and the energy storage efficiency. The adoption of active heat transfer enhancement (convective heat transfer enhancement) leads to a high energy storage density of 670 MJ m−3 (close to the maximum theoretical value of 755.3 MJ m−3). In contrast, the energy storage efficiency decreases dramatically due to the increase in the pumping power. On the other hand, passive heat transfer techniques using the bed’s thermal conductivity enhancers provide a balance between the energy storage density (578 MJ m−3) and the energy efficiency (74%). The utilization of phase change material as an internal heat recovery medium leads to a further reduction in the heat storage performance indicators (142 MJ m−3 and 49%). Nevertheless, such a system combining thermochemical and latent heat storage, if properly optimized, can be promising for thermal energy storage applications.


Energies ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3105
Author(s):  
Mohamed Zbair ◽  
Simona Bennici

To improve the proficiency of energy systems in addition to increasing the usage of renewable energies, thermal energy storage (TES) is a strategic path. The present literature review reports an overview of the recent advancements in the utilization of salt hydrates (single or binary mixtures) and composites as sorbents for sorption heat storage. Starting by introducing various heat storage systems, the operating concept of the adsorption TES was clarified and contrasted to other technologies. Consequently, a deep examination and crucial problems related to the different types of salt hydrates and adsorbents were performed. Recent advances in the composite materials used in sorption heat storage were also reviewed and compared. A deep discussion related to safety, price, availability, and hydrothermal stability issues is reported. Salt hydrates display high theoretical energy densities, which are promising materials in TES. However, they show a number of drawbacks for use in the basic state including low temperature overhydration and deliquescence (e.g., MgCl2), high temperature degradation, sluggish kinetics leading to a low temperature rise (e.g., MgSO4), corrosiveness and toxicity (e.g., Na2S), and low mass transport due to the material macrostructure. The biggest advantage of adsorption materials is that they are more hydrothermally stable. However, since adsorption is the most common sorption phenomenon, such materials have a lower energy content. Furthermore, when compared to salt hydrates, they have higher prices per mass, which reduces their appeal even further when combined with lower energy densities. Economies of scale and the optimization of manufacturing processes may help cut costs. Among the zeolites, Zeolite 13X is among the most promising. Temperature lifts of 35–45 °C were reached in lab-scale reactors and micro-scale experiments under the device operating settings. Although the key disadvantage is an excessively high desorption temperature, which is problematic to attain using heat sources, for instance, solar thermal collectors. To increase the energy densities and enhance the stability of adsorbents, composite materials have been examined to ameliorate the stability and to achieve suitable energy densities. Based on the reviewed materials, MgSO4 has been identified as the most promising salt; it presents a higher energy density compared to other salts and can be impregnated in a porous matrix to prepare composites in order to overcome the drawbacks connected to its use as pure salt. However, due to pore volume reduction, potential deliquescence and salt leakage from the composite as well as degradation, issues with heat and mass transport can still exist. In addition, to increase the kinetics, stability, and energy density, the use of binary salt deposited in a porous matrix is suitable. Nevertheless, this solution should take into account the deliquescence, safety, and cost of the selected salts. Therefore, binary systems can be the solution to design innovative materials with predetermined sorption properties adapted to particular sorption heat storage cycles. Finally, working condition, desorption temperature, material costs, lifetime, and reparation, among others, are the essential point for commercial competitiveness. High material costs and desorption temperatures, combined with lower energy densities under normal device operating conditions, decrease their market attractiveness. As a result, the introduction of performance metrics within the scientific community and the use of economic features on a material scale are suggested.


Author(s):  
Helena Schneider ◽  
Lucas K. Schindel ◽  
Lucas B. Gomes ◽  
Isabel C. Tessaro ◽  
Nilson R. Marcilio

2018 ◽  
Vol 6 (3) ◽  
pp. 035503 ◽  
Author(s):  
Qiwei Shi ◽  
Jianxiong Liu ◽  
Jianzheng Zhen ◽  
Guanqun Zhang ◽  
Cheng Liu ◽  
...  

2018 ◽  
Vol 157 ◽  
pp. 619-630 ◽  
Author(s):  
Qinghua Yu ◽  
Alessandro Romagnoli ◽  
Bushra Al-Duri ◽  
Danmei Xie ◽  
Yulong Ding ◽  
...  

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