scholarly journals Research Status and Prospect on Vanadium-Based Catalysts for NH3-SCR Denitration

Materials ◽  
2018 ◽  
Vol 11 (9) ◽  
pp. 1632 ◽  
Author(s):  
Jie Zhang ◽  
Xiangcheng Li ◽  
Pingan Chen ◽  
Boquan Zhu
Keyword(s):  
Active Sites ◽  
Catalytic Mechanism ◽  
Surface Defects ◽  
Catalytic Reduction ◽  
Surface Acidity ◽  
Industrial Applications ◽  
Future Research ◽  
Medium Temperature ◽  
Temperature Range ◽  
Vanadium Based Catalysts

Selective catalytic reduction of NOx with NH3 is one of the most widely used technologies in denitration. Vanadium-based catalysts have been extensively studied for the deNOx process. V2O5/WO3(MoO3)TiO2 as a commercial catalyst has excellent catalytic activity in the medium temperature range. However, it has usually faced several problems in practical industrial applications, including narrow windows of operation temperatures, and the deactivation of catalysts. The modification of vanadium-based catalysts will be the focus in future research. In this paper, the chemical composition of vanadium-based catalysts, catalytic mechanism, the broadening of the temperature range, and the improvement of erosion resistance are reviewed. Furthermore, the effects of four major systems of copper, iron, cerium and manganese on the modification of vanadium-based catalysts are introduced and analyzed. It is worth noting that the addition of modified elements as promoters has greatly improved the catalytic performance. They can enhance the surface acidity, which leads to the increasing adsorption capacity of NH3. Surface defects and oxygen vacancies have also been increased, resulting in more active sites. Finally, the future development of vanadium-based catalysts for denitration is prospected. It is indicated that the main purpose for the research of vanadium-based modification will help to obtain safe, environmentally friendly, efficient, and economical catalysts.

Research Progress of Low-Temperature SCR DeNOx Catalysts

2013 ◽  
Vol 320 ◽  
pp. 629-638 ◽  
Author(s):  
Yun Sang Feng ◽  
Shao Guang Liu ◽  
Cheng Wu Chen ◽  
He Yong Zhao ◽  
Yu Song Xu
Keyword(s):  
Low Temperature ◽  
Active Sites ◽  
Noble Metals ◽  
Research Progress ◽  
Future Research ◽  
Affecting Factors ◽  
Medium Temperature ◽  
Denox Catalysts ◽  
Temperature Activation ◽  
Low Temperature Scr

Low-temperature SCR DeNOx process is considered to be a potential technique to meet the stringent environment regulations. It can avoid the problem such as blocking and eroding often generated in medium temperature, polluting and poisoning caused by alkali elements and so on. In this paper, a review of DeNOx catalysts about noble metals, molecular sieve, carbon-based and metal oxides catalyst was presented. The affecting factors of the low-temperature activation were comprehensively expounded, such as precursor introduction method, preparation method, supporter pretreatment and catalyst structure. Then mechanism of SO2 poisoning and effect of active compositions were analyzed. The dual effect of SO2 on the activity of low temperature catalysts mainly results from the formation of certain sulfur-containing species on catalyst surface. Water vapor decreased the number of available active sites attributed to competitive adsorption among H2O and other reactants. Moreover, the co-existence of H2O and SO2 resulted in the decrease of activity obviously. So the way to improve resistance of SO2 and H2O poisoning was summed up. Finally, future research and development directions in the developing low-temperature SCR for removal of NOx technology were proposed.

scholarly journals Experimental Study on the Deactivating Effect of KNO3, KCl, and K2SO4on Nanosized Ceria/Titania SCR Catalyst

2015 ◽  
Vol 2015 ◽  
pp. 1-10
Author(s):  
Xiongbo Chen ◽  
Ping Fang ◽  
Wenhao Zeng ◽  
Kunyuan Liu ◽  
Zhixiong Tang ◽  
...  
Keyword(s):  
Oxygen Diffusion ◽  
Surface Defects ◽  
Catalytic Reduction ◽  
Surface Acidity ◽  
Acid Sites ◽  
Ammonia Adsorption ◽  
Scr Catalyst ◽  
No Conversion ◽  
Ceria Reduction ◽  
Potassium Addition

Nanosized Ce/TiO2is effective in selective catalytic reduction of NO with NH3. The NO conversion of Ce/TiO2is 93% at 370°C. However, addition of potassium using KNO3, KCl, or K2SO4as precursors effectively deactivates Ce/TiO2. NO conversion at 370°C is reduced to 45%, 24%, and 16% after addition of KNO3, KCl, and K2SO4, respectively, with a controlled K/Ce molar ration at 0.25. The deactivation may be attributed to the changes in the structural and chemical state of ceria and the degradation of surface acidity. The transformation of amorphous ceria into ceria crystals after potassium addition, together with the decrease of surface defects, is also determined. Oxygen diffusion in the process of ceria reduction is slow, and the redox cycle is slowed down. Moreover, the surface acid sites are markedly destroyed, leading to the reduced capacity of ammonia adsorption. These results may provide useful information for the application and life management of CeO2/TiO2in potassium-rich environments such as biofuel-fired boilers.

Structure of Hydrogenase in Biohydrogen Production Anaerobic Bacteria

2011 ◽  
pp. 251-258 ◽  
Author(s):  
Ming Du ◽  
Lu Zhang
Keyword(s):  
Active Site ◽  
Active Sites ◽  
Catalytic Mechanism ◽  
Anaerobic Bacteria ◽  
Research Direction ◽  
Biohydrogen Production ◽  
Future Research ◽  
Hydrogen Energy ◽  
Industrialization Process ◽  
Catalytic Mechanisms

Hydrogenase plays an important role in the process of biohydrogen production. Hydrogenases have very unique active sites and are classified into three groups according to the metal composition of the active sites: the [Ni-Fe] hydrogenase, [Fe-Fe] hydrogenase, and [Fe-only] hydrogenase. In this paper, the crystal structures and active sites of three kinds of hydrogenases are examined and compared. These enzymes have an unusual structural feature in common. Their similar active site indicates that the catalytic mechanism of hydrogen activation is probably similar. The understanding of the catalytic mechanisms for the three kinds of hydrogenases may help achieve the industrialization process of hydrogen energy production. Moreover, the future research direction about the hydrogenases from auto-aggregative bacteria and the chemical mimic of hydrogenases structure is discussed.

scholarly journals Polyelectrolyte Gels: A Unique Class of Soft Materials

Gels ◽  
2021 ◽  
Vol 7 (3) ◽  
pp. 102
Author(s):  
Ferenc Horkay
Keyword(s):  
Exchange Process ◽  
Interaction Strength ◽  
Soft Materials ◽  
Industrial Applications ◽  
Future Research ◽  
Swelling Kinetics ◽  
Polyelectrolyte Gels ◽  
Ion Exchange Process ◽  
Counter Ions ◽  
Kinetics Of

The objective of this article is to introduce the readers to the field of polyelectrolyte gels. These materials are common in living systems and have great importance in many biomedical and industrial applications. In the first part of this paper, we briefly review some characteristic properties of polymer gels with an emphasis on the unique features of this type of soft material. Unsolved problems and possible future research directions are highlighted. In the second part, we focus on the typical behavior of polyelectrolyte gels. Many biological materials (e.g., tissues) are charged (mainly anionic) polyelectrolyte gels. Examples are shown to illustrate the effect of counter-ions on the osmotic swelling behavior and the kinetics of the swelling of model polyelectrolyte gels. These systems exhibit a volume transition as the concentration of higher valence counter-ions is gradually increased in the equilibrium bath. A hierarchy is established in the interaction strength between the cations and charged polymer molecules according to the chemical group to which the ions belong. The swelling kinetics of sodium polyacrylate hydrogels is investigated in NaCl solutions and in solutions containing both NaCl and CaCl2. In the presence of higher valence counter-ions, the swelling/shrinking behavior of these gels is governed by the diffusion of free ions in the swollen network, the ion exchange process and the coexistence of swollen and collapsed states.

scholarly journals An Experimental Study of the Decomposition and Carbonation of Magnesium Carbonate for Medium Temperature Thermochemical Energy Storage

Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1316
Author(s):  
Daniel Mahon ◽  
Gianfranco Claudio ◽  
Philip Eames
Keyword(s):  
Thermal Analysis ◽  
Thermal Decomposition ◽  
Energy Storage ◽  
Magnesium Carbonate ◽  
Experimental Results ◽  
Future Research ◽  
Medium Temperature ◽  
Different Temperatures ◽  
Decomposition Enthalpy ◽  
Co2 Atmosphere

To improve the energy efficiency of an industrial process thermochemical energy storage (TCES) can be used to store excess or typically wasted thermal energy for utilisation later. Magnesium carbonate (MgCO3) has a turning temperature of 396 °C, a theoretical potential to store 1387 J/g and is low cost (~GBP 400/1000 kg). Research studies that assess MgCO3 for use as a medium temperature TCES material are lacking, and, given its theoretical potential, research to address this is required. Decomposition (charging) tests and carbonation (discharging) tests at a range of different temperatures and pressures, with selected different gases used during the decomposition tests, were conducted to gain a better understanding of the real potential of MgCO3 for medium temperature TCES. The thermal decomposition (charging) of MgCO3 has been investigated using thermal analysis techniques including simultaneous thermogravimetric analysis and differential scanning calorimetry (TGA/DSC), TGA with attached residual gas analyser (RGA) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) (up to 650 °C). TGA, DSC and RGA data have been used to quantify the thermal decomposition enthalpy from each MgCO3.xH2O thermal decomposition step and separate the enthalpy from CO2 decomposition and H2O decomposition. Thermal analysis experiments were conducted at different temperatures and pressures (up to 40 bar) in a CO2 atmosphere to investigate the carbonation (discharging) and reversibility of the decarbonation–carbonation reactions for MgCO3. Experimental results have shown that MgCO3.xH2O has a three-step thermal decomposition, with a total decomposition enthalpy of ~1050 J/g under a nitrogen atmosphere. After normalisation the decomposition enthalpy due to CO2 loss equates to 1030–1054 J/g. A CO2 atmosphere is shown to change the thermal decomposition (charging) of MgCO3.xH2O, requiring a higher final temperature of ~630 °C to complete the decarbonation. The charging input power of MgCO3.xH2O was shown to vary from 4 to 8136 W/kg with different isothermal temperatures. The carbonation (discharging) of MgO was found to be problematic at pressures up to 40 bar in a pure CO2 atmosphere. The experimental results presented show MgCO3 has some characteristics that make it a candidate for thermochemical energy storage (high energy storage potential) and other characteristics that are problematic for its use (slow discharge) under the experimental test conditions. This study provides a comprehensive foundation for future research assessing the feasibility of using MgCO3 as a medium temperature TCES material. Future research to determine conditions that improve the carbonation (discharging) process of MgO is required.

scholarly journals Ferrierite and Its Delaminated Forms Modified with Copper as Effective Catalysts for NH3-SCO Process

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4885
Author(s):  
Aneta Święs ◽  
Małgorzata Rutkowska ◽  
Andrzej Kowalczyk ◽  
Urbano Díaz ◽  
Antonio E. Palomares ◽  
...  
Keyword(s):  
Copper Oxide ◽  
Ammonia Oxidation ◽  
Catalytic Reduction ◽  
Surface Acidity ◽  
Selective Reduction ◽  
Exchange Method ◽  
Copper Species ◽  
Selective Catalytic Oxidation ◽  
Catalytically Active ◽  
Copper Cations

Ferrierites and their delaminated forms (ITQ-6), containing aluminum or titanium in the zeolite framework, were synthetized and modified with copper by an ion-exchange method. The obtained samples were characterized with respect to their chemical composition (ICP-OES), structure (XRD, UV-Vis DRS), textural parameters (N2-sorption), surface acidity (NH3-TPD), form and reducibility of deposited copper species (UV-Vis DRS and H2-TPR). Ferrierites and delaminated ITQ-6 zeolites modified with copper were studied as catalysts for the selective catalytic oxidation of ammonia to dinitrogen (NH3-SCO). It was shown that aggregated copper oxide species, which were preferentially formed on Ti-zeolites, were catalytically active in direct low-temperature ammonia oxidation to NO, while copper introduced into Al-zeolites was present mainly in the form of monomeric copper cations catalytically active in selective reduction of NO by ammonia to dinitrogen. It was postulated that ammonia oxidation in the presence of the studied catalysts proceeds according to the internal-selective catalytic reduction mechanism (i-SCR) and therefore the suitable ratio between aggregated copper oxide species and monomeric copper cations is necessary to obtain active and selective catalysts for the NH3-SCO process. Cu/Al-ITQ-6 presented the best catalytic properties possibly due to the most optimal ratio of these copper species.

scholarly journals Enhanced catalytic ozonation of ibuprofen using a 3D structured catalyst with MnO2 nanosheets on carbon microfibers

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Guhankumar Ponnusamy ◽  
Hajar Farzaneh ◽  
Yongfeng Tong ◽  
Jenny Lawler ◽  
Zhaoyang Liu ◽  
...  
Keyword(s):  
Removal Efficiency ◽  
Active Sites ◽  
Low Cost ◽  
Three Dimensional ◽  
Industrial Applications ◽  
Catalytic Ozonation ◽  
Heterogeneous Catalytic ◽  
Structured Catalyst ◽  
Dimensional Network ◽  
Carbon Microfibers

AbstractHeterogeneous catalytic ozonation is an effective approach to degrade refractory organic pollutants in water. However, ozonation catalysts with combined merits of high activity, good reusability and low cost for practical industrial applications are still rare. This study aims to develop an efficient, stable and economic ozonation catalyst for the degradation of Ibuprofen, a pharmaceutical compound frequently detected as a refractory pollutant in treated wastewaters. The novel three-dimensional network-structured catalyst, comprising of δ-MnO2 nanosheets grown on woven carbon microfibers (MnO2 nanosheets/carbon microfiber), was synthesized via a facile hydrothermal approach. Catalytic ozonation performance of Ibuprofen removal in water using the new catalyst proves a significant enhancement, where Ibuprofen removal efficiency of close to 90% was achieved with a catalyst loading of 1% (w/v). In contrast, conventional ozonation was only able to achieve 65% removal efficiency under the same operating condition. The enhanced performance with the new catalyst could be attributed to its significantly increased available surface active sites and improved mass transfer of reaction media, as a result of the special surface and structure properties of this new three-dimensional network-structured catalyst. Moreover, the new catalyst displays excellent stability and reusability for ibuprofen degradation over successive reaction cycles. The facile synthesis method and low-cost materials render the new catalyst high potential for industrial scaling up. With the combined advantages of high efficiency, high stability, and low cost, this study sheds new light for industrial applications of ozonation catalysts.

scholarly journals A Compact Review of Laser Welding Technologies for Amorphous Alloys

Metals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1690
Author(s):  
Jian Qiao ◽  
Peng Yu ◽  
Yanxiong Wu ◽  
Taixi Chen ◽  
Yixin Du ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Laser Welding ◽  
Amorphous Alloys ◽  
High Energy ◽  
Industrial Applications ◽  
High Energy Density ◽  
Current Status ◽  
Future Research ◽  
Technological Parameters ◽  
Fast Heating

Amorphous alloys have emerged as important materials for precision machinery, energy conversion, information processing, and aerospace components. This is due to their unique structure and excellent properties, including superior strength, high elasticity, and excellent corrosion resistance, which have attracted the attention of many researchers. However, the size of the amorphous alloy components remains limited, which affects industrial applications. Significant developments in connection with this technology are urgently needed. Laser welding represents an efficient welding method that uses a laser beam with high energy-density for heating. Laser welding has gradually become a research hotspot as a joining method for amorphous alloys due to its fast heating and cooling rates. In this compact review, the current status of research into amorphous-alloy laser welding technology is discussed, the influence of technological parameters and other welding conditions on welding quality is analyzed, and an outlook on future research and development is provided. This paper can serve as a useful reference for both fundamental research and engineering applications in this field.

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