scholarly journals Aluminium-induced component engineering of mesoporous composite materials for low-temperature NH3-SCR

2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Ge Li ◽  
Baodong Wang ◽  
Ziran Ma ◽  
Hongyan Wang ◽  
Jing Ma ◽  
...  
2016 ◽  
Vol 31 (6) ◽  
pp. 561
Author(s):  
FAN Gui-Fen ◽  
XU Xing ◽  
WANG Kai ◽  
LV Wen-Zhong ◽  
LIANG Fei ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 618
Author(s):  
Huan Du ◽  
Zhitao Han ◽  
Xitian Wu ◽  
Chenglong Li ◽  
Yu Gao ◽  
...  

Er-modified FeMn/TiO2 catalysts were prepared through the wet impregnation method, and their NH3-SCR activities were tested. The results showed that Er modification could obviously promote SO2 resistance of FeMn/TiO2 catalysts at a low temperature. The promoting effect and mechanism were explored in detail using various techniques, such as BET, XRD, H2-TPR, XPS, TG, and in-situ DRIFTS. The characterization results indicated that Er modification on FeMn/TiO2 catalysts could increase the Mn4+ concentration and surface chemisorbed labile oxygen ratio, which was favorable for NO oxidation to NO2, further accelerating low-temperature SCR activity through the “fast SCR” reaction. As fast SCR reaction could accelerate the consumption of adsorbed NH3 species, it would benefit to restrain the competitive adsorption of SO2 and limit the reaction between adsorbed SO2 and NH3 species. XPS results indicated that ammonium sulfates and Mn sulfates formed were found on Er-modified FeMn/TiO2 catalyst surface seemed much less than those on FeMn/TiO2 catalyst surface, suggested that Er modification was helpful for reducing the generation or deposition of sulfate salts on the catalyst surface. According to in-situ DRIFTS the results of, the presence of SO2 in feeding gas imposed a stronger impact on the NO adsorption than NH3 adsorption on Lewis acid sites of Er-modified FeMn/TiO2 catalysts, gradually making NH3-SCR reaction to proceed in E–R mechanism rather than L–H mechanism. DRIFTS.


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.


2021 ◽  
Vol 49 (1) ◽  
pp. 113-120
Author(s):  
Dong-jie YAN ◽  
Tong GUO ◽  
Ya YU ◽  
Zhao-hui CHEN

Fuel ◽  
2021 ◽  
Vol 303 ◽  
pp. 121239
Author(s):  
Zhiping Zhang ◽  
Yingying Li ◽  
Piaoping Yang ◽  
Yushi Li ◽  
Chen Zhao ◽  
...  

2021 ◽  
Vol 9 (5) ◽  
pp. 106323
Author(s):  
Yuhan Zhou ◽  
Buxin Su ◽  
Shan Ren ◽  
Zhichao Chen ◽  
Zenghui Su ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4273
Author(s):  
Jian Zhang ◽  
Xiaojun Wang ◽  
Xinjun Fu

Chopped carbon fiber-reinforced low-density unsaturated polyester resin (CCFR-LDUPR) composite materials with light weight and high mechanical properties were prepared at low temperature and under the synergistic action of methyl ethyl ketone peroxide (MEKP-II) and cobalt naphthenate. Optimal preparation conditions were obtained through an orthogonal experiment, which were preparation temperature at 58.0 °C, 2.00 parts per hundred of resin (phr) of NH4HCO3, 4.00 phr of chopped carbon fibers (CCFs) in a length of 6.0 mm, 1.25 phr of initiator and 0.08 phr of cobalt naphthenate. CCFR-LDUPR composite sample presented its optimal properties for which the density (ρ) was 0.58 ± 0.02 g·cm−3 and the specific compressive strength (Ps) was 53.56 ± 0.83 MPa·g−1·cm3, which is 38.9% higher than that of chopped glass fiber-reinforced low-density unsaturated polyester resin (CGFR-LDUPR) composite materials. Synergistic effects of initiator and accelerator accelerated the specific polymerization of resin in facile preparation at low temperature. Unique “dimples”, “plate microstructure” and “surface defect” fabricated the specific microstructure of the matrix of CCFR-LDUPR composite samples, which was different from that of cured unsaturated polyester resin (UPR) with “body defect” or that of CGFR-LDUPR with coexistence of “surface defect” and “body defect”.


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