scholarly journals Surface Area Modification of Natural Zeolite Through NaCl Counterbalanced Treatment to Apply in Adsorption Heat Storage System

Evergreen ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. 26-31
Author(s):  
Euis Djubaedah ◽  
Arum Wulandari ◽  
Nasruddin ◽  
K. Krisnandi
2019 ◽  
Vol 147 ◽  
pp. 10-28 ◽  
Author(s):  
Hesham O. Helaly ◽  
Mohamed M. Awad ◽  
Ibrahim I. El-Sharkawy ◽  
Ahmed M. Hamed

Energy ◽  
2021 ◽  
pp. 122327
Author(s):  
Ting Yan ◽  
Hong Zhang ◽  
Nan Yu ◽  
Dong Li ◽  
Q.W. Pan

Author(s):  
Reza Yazdanpanah ◽  
Eshagh Moradiyan ◽  
Rouein Halladj ◽  
Sima Askari

Aim and Objective: The research focuses on recent progress in the production of light olefins. Hence, the common catalyst of the reaction (SAPO-34) deactivates quickly because of coke formation, we reorganized the mechanism combining SAPO-34 with a natural zeolite in order to delay the deactivation time. Materials and Methods: The synthesis of nanocomposite catalyst was conducted hydrothermally using experimental design. Firstly, Clinoptilolite was modified using nitric acid in order to achieve nano scaled material. Then, the initial gel of the SAPO-34 was prepared using DEA, aluminum isopropoxide, phosphoric acid and TEOS as the organic template, sources of Aluminum, Phosphor, and Silicate, respectively. Finally, the modified zeolite was combined with SAPO-34's gel. Results: 20 different catalysts due to D-Optimal design were synthesized and the nanocomposite with 50 weight percent of SAPO-34, 4 hours Crystallization and early Clinoptilolite precipitation showed the highest relative crystallinity, partly high BET surface area and hierarchical structure. Conclusion: Different analysis illustrated the existence of both components. The most important property alteration of nanocomposite was the increment of pore mean diameters and reduction in pore volumes in comparison with free SAPO-34. Due to low price of Clinoptilolite, the new catalyst develops the economy of the process. Using this composite, according to formation of multi-sized pores located hierarchically on the surface of the catalyst and increased surface area, significant amounts of Ethylene and Propylene, in comparison with free SAPO-34, were produced, as well as deactivation time that was improved.


Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 217
Author(s):  
Marin Ugrina ◽  
Martin Gaberšek ◽  
Aleksandra Daković ◽  
Ivona Nuić

Sulfur-impregnated zeolite has been obtained from the natural zeolite clinoptilolite by chemical modification with Na2S at 150 °C. The purpose of zeolite impregnation was to enhance the sorption of Hg(II) from aqueous solutions. Chemical analysis, acid and basic properties determined by Bohem’s method, chemical behavior at different pHo values, zeta potential, cation-exchange capacity (CEC), specific surface area, X-ray powder diffraction (XRPD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetry with derivative thermogravimetry (TG-DTG) were used for detailed comparative mineralogical and physico-chemical characterization of natural and sulfur-impregnated zeolites. Results revealed that the surface of the natural zeolite was successfully impregnated with sulfur species in the form of FeS and CaS. Chemical modification caused an increase in basicity and the net negative surface charge due to an increase in oxygen-containing functional groups as well as a decrease in specific surface area and crystallinity due to the formation of sulfur-containing clusters at the zeolite surface. The sorption of Hg(II) species onto the sulfur-impregnated zeolite was affected by the pH, solid/liquid ratio, initial Hg(II) concentration, and contact time. The optimal sorption conditions were determined as pH 2, a solid/liquid ratio of 10 g/L, and a contact time of 800 min. The maximum obtained sorption capacity of the sulfur-impregnated zeolite toward Hg(II) was 1.02 mmol/g. The sorption mechanism of Hg(II) onto the sulfur-impregnated zeolite involves electrostatic attraction, ion exchange, and surface complexation, accompanied by co-precipitation of Hg(II) in the form of HgS. It was found that sulfur-impregnation enhanced the sorption of Hg(II) by 3.6 times compared to the natural zeolite. The leaching test indicated the retention of Hg(II) in the zeolite structure over a wide pH range, making this sulfur-impregnated sorbent a promising material for the remediation of a mercury-polluted environment.


Energies ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3129
Author(s):  
Jewon Oh ◽  
Daisuke Sumiyoshi ◽  
Masatoshi Nishioka ◽  
Hyunbae Kim

The mass introduction of renewable energy is essential to reduce carbon dioxide emissions. We examined an operation method that combines the surplus energy of photovoltaic power generation using demand response (DR), which recognizes the balance between power supply and demand, with an aquifer heat storage system. In the case that predicts the occurrence of DR and performs DR storage and heat dissipation operation, the result was an operation that can suppress daytime power consumption without increasing total power consumption. Case 1-2, which performs nighttime heat storage operation for about 6 h, has become an operation that suppresses daytime power consumption by more than 60%. Furthermore, the increase in total power consumption was suppressed by combining DR heat storage operation. The long night heat storage operation did not use up the heat storage amount. Therefore, it is recommended to the heat storage operation at night as much as possible before DR occurs. In the target area of this study, the underground temperature was 19.1 °C, the room temperature during cooling was about 25 °C and groundwater could be used as the heat source. The aquifer thermal energy storage (ATES) system in this study uses three wells, and consists of a well that pumps groundwater, a heat storage well that stores heat and a well that used heat and then returns it. Care must be taken using such an operation method depending on the layer configuration.


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