scholarly journals Dyes Degradation with Fe-Doped Titanium Nanotube Photocatalysts Prepared from Spend Steel Slag

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Chih Ming Ma ◽  
Yu Jung Lin ◽  
Ren Wei Shiue ◽  
Chang Tang Chang
Keyword(s):  
Catalytic Activity ◽  
High Stability ◽  
Waste Treatment ◽  
Steel Slag ◽  
Degradation Efficiency ◽  
High Catalytic Activity ◽  
Electron Hole ◽  
Generate Electron ◽  
Direct Black 22 ◽  
Dyes Degradation

TiO2has been studied most commonly because it has high stability, nontoxicity, high catalytic activity, and high conductivity. Many studies have shown that TiO2would generate electron-hole pairs illuminated with UV and surround more energy than that before being illuminated. In this study, the titanium nanotube (TNT) photocatalysts were prepared to increase the surface area and adsorption capacity. The Fe TNT was also prepared from a slag iron since many slag irons cause waste treatment problems. In this study, a different Fe loading was also assessed since TNT doped with metals can be used to improve the degradation efficiency. Furthermore, five kinds of dye concentration, including 10, 20, 100, 200, and 400 ppm, and five kinds of Fe-doped content, including 0, 0.77, 1.13, 2.24, and 4.50%, were tested. Different kinds of reaction time and dye species were also assessed. In this result, Direct Black 22 was the most difficult to be degraded, although the concentration was decreased or the dose amount was increased. The degradation efficiency of 10 ppm Direct Black 22 was below 40% with 0.04 gL−1TNT under 365 nm UV irradiation.

Sulfur doping enhanced desorption of intermediates on NiCoP for efficient alkaline hydrogen evolution

Nanoscale ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 1985-1993 ◽  
Author(s):  
Yuyang Qi ◽  
Long Zhang ◽  
Lan Sun ◽  
Guanjun Chen ◽  
Qiaomei Luo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
High Stability ◽  
Low Cost ◽  
High Catalytic Activity ◽  
Sulfur Doping

Electrocatalysts with high catalytic activity, high stability and low cost are critical to the hydrogen evolution reaction (HER).

scholarly journals Highly effective photocatalytic performance of {001}-TiO2/MoS2/RGO hybrid heterostructures for the reduction of Rh B

RSC Advances ◽  
2019 ◽  
Vol 9 (26) ◽  
pp. 15033-15041 ◽  
Author(s):  
Ya Gao ◽  
Yongjie Zheng ◽  
Jixing Chai ◽  
Jingzhi Tian ◽  
Tao Jing ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Photocatalytic Performance ◽  
Photogenerated Electron ◽  
High Catalytic Activity ◽  
Electron Hole ◽  
Co Catalysts ◽  
Effective Separation ◽  
Key Features ◽  
Rapid Transfer ◽  
Photocatalytic Materials

Effective separation and rapid transfer of photogenerated electron–hole pairs are key features of photocatalytic materials with high catalytic activity, which could be achieved by co-catalysts.

High catalytic activity and stability of nickel sulfide and cobalt sulfide hierarchical nanospheres on the counter electrodes for dye-sensitized solar cells

2014 ◽  
Vol 50 (37) ◽  
pp. 4824-4826 ◽  
Author(s):  
Jie Yang ◽  
Chunxiong Bao ◽  
Kai Zhu ◽  
Tao Yu ◽  
Faming Li ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
High Stability ◽  
Nickel Sulfide ◽  
Dye Sensitized Solar Cells ◽  
Cobalt Sulfide ◽  
High Catalytic Activity ◽  
Counter Electrodes ◽  
Dye Sensitized ◽  
Sensitized Solar Cells

In situ grown hierarchical nickel sulfide and cobalt sulfide nanospheres on the counter electrodes with high catalytic activity and high stability.

High-efficiency photo-oxidation of thioethers over C60@PCN-222 under air

2019 ◽  
Vol 7 (38) ◽  
pp. 22084-22091 ◽  
Author(s):  
Deng-Yue Zheng ◽  
En-Xuan Chen ◽  
Chun-Rong Ye ◽  
Xiao-Chun Huang
Keyword(s):  
Catalytic Activity ◽  
Photocatalytic Oxidation ◽  
High Efficiency ◽  
Photogenerated Electron ◽  
High Catalytic Activity ◽  
Electron Hole ◽  
Photo Oxidation ◽  
First Time

For the first time, fullerene (C60) was used to enhance the photogenerated electron–hole separation of MOFs as a catalyst and showed high catalytic activity in the photocatalytic oxidation of thioether in air.

Enhanced catalytic activity of low-Pt content nanocatalysts supported on hollow carbon spheres for the ORR in alkaline media

MRS Advances ◽  
2020 ◽  
Vol 5 (57-58) ◽  
pp. 2961-2972
Author(s):  
P.C. Meléndez-González ◽  
E. Garza-Duran ◽  
J.C. Martínez-Loyola ◽  
P. Quintana-Owen ◽  
I.L. Alonso-Lemus ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Anion Exchange ◽  
Average Particle Size ◽  
Synthesis Method ◽  
Alkaline Media ◽  
High Catalytic Activity ◽  
Average Particle ◽  
Carbon Spheres ◽  
Hollow Carbon ◽  
Hollow Carbon Spheres

In this work, low-Pt content nanocatalysts (≈ 5 wt. %) supported on Hollow Carbon Spheres (HCS) were synthesized by two routes: i) colloidal conventional polyol, and ii) surfactant-free Bromide Anion Exchange (BAE). The nanocatalysts were labelled as Pt/HCS-P and Pt/HCS-B for polyol and BAE, respectively. The physicochemical characterization of the nanocatalysts showed that by following both methods, a good control of chemical composition was achieved, obtaining in addition well dispersed nanoparticles of less than 3 nm TEM average particle size (d) on the HCS. Pt/HCS-B contained more Pt0 species than Pt/HCS-P, an effect of the synthesis method. In addition, the structure of the HCS remains more ordered after BAE synthesis, compared to polyol. Regarding the catalytic activity for the Oxygen Reduction Reaction (ORR) in 0.5 M KOH, Pt/HCS-P and Pt/HCS-B showed a similar performance in terms of current density (j) at 0.9 V vs. RHE than the benchmark commercial 20 wt. % Pt/C. However, Pt/HCS-P and Pt/HCS-B demonstrated a 6 and 5-fold increase in mass catalytic activity compared to Pt/C, respectively. A positive effect of the high specific surface area of the HCS and its interactions with metal nanoparticles and electrolyte, which promoted the mass transfer, increased the performance of Pt/HCS-P and Pt/HCS-B. The high catalytic activity showed by Pt/HCS-B and Pt/HCS-P for the ORR, even with a low-Pt content, make them promising cathode nanocatalysts for Anion Exchange Membrane Fuel Cells (AEMFC).

Ordered Intermetallic Nanoparticles with High Catalytic Activity Prepared by an Electrochemically Induced Phase Transformation

2019 ◽  
Author(s):  
Du Sun ◽  
yunfei wang ◽  
Kenneth Livi ◽  
chuhong wang ◽  
ruichun luo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffusion Mechanism ◽  
Reduction Reaction ◽  
Atomic Scale ◽  
High Catalytic Activity ◽  
Ambient Conditions ◽  
Magnetic Devices ◽  
Disordered Alloys ◽  
Ordered Intermetallic ◽  
Intermetallic Nanoparticles

<div> <p>The synthesis of alloys with long range atomic scale ordering (ordered intermetallics) is an emerging field of nanochemistry. Ordered intermetallic nanoparticles are useful for a wide variety of applications such as catalysis, superconductors, and magnetic devices. However, the preparation of nanostructured ordered intermetallics is challenging in comparison to disordered alloys, hindering progress in materials development. We report a process for converting colloidally synthesized ordered intermetallic PdBi<sub>2</sub> to ordered intermetallic Pd<sub>3</sub>Bi nanoparticles under ambient conditions by an electrochemically induced phase transition. The low melting point of PdBi<sub>2</sub> corresponds to low vacancy formation energies which enables the facile removal of the Bi from the surface, while simultaneously enabling interdiffusion of the constituent atoms via a vacancy diffusion mechanism under ambient conditions. The resulting phase-converted ordered intermetallic Pd<sub>3</sub>Bi exhibits 11x and 3.5x higher mass activty and high methanol tolerance for the oxygen reduction reaction compared to Pt/C and Pd/C, respectively,which is the highest reported for a Pd-based catalyst, to the best of our knowledge. These results establish a key development in the synthesis of noble metal rich ordered intermetallic phases with high catalytic activity, and sets forth guidelines for the design of ordered intermetallic compounds under ambient conditions.</p> </div>

Nickel (II) and oxovanadium (IV) complexes supported on MCM-41 mesoporous and their application in catalytic selective sulfide and thiol oxidation

2020 ◽  
Vol 23 ◽  
Author(s):  
Mohsen Nikoorazm ◽  
Maryam Khanmoradi ◽  
Masoumeh Sayadian
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Sol Gel ◽  
Reaction Times ◽  
Significant Loss ◽  
Spectral Studies ◽  
High Catalytic Activity ◽  
Catalytic Systems ◽  
Solvent Free Conditions ◽  
Mcm 41

Introduction:: MCM-41 was synthesized using the sol-gel method. Then two new transition metal complexes of Nickel (II) and Vanadium (IV), were synthesized by immobilization of adenine (6-aminopurine) into MCM-41 mesoporous. The compounds have been characterized by XRD, TGA, SEM, AAS and FT-IR spectral studies. Using these catalysts provided an efficient and enantioselective procedure for oxidation of sulfides to sulfoxides and oxidative coupling of thiols to their corresponding disulfides using hydrogen peroxide at room temperature. Materials and Methods:: To a solution of sulfide or thiol (1 mmol) and H2O2 (5 mmol), a determined amount of the catalyst was added. The reaction mixture was stirred at room temperature for the specific time under solvent free conditions. The progress of the reaction was monitored by TLC using n-hexane: acetone (8:2). Afterwards, the catalyst was removed from the reaction mixture by centrifugation and, then, washed with dichloromethane in order to give the pure products. Results:: All the products were obtained in excellent yields and short reaction times indicating the high activity of the synthesized catalysts. Besides, the catalysts can be recovered and reused for several runs without significant loss in their catalytic activity. Conclusion:: These catalytic systems furnish the products very quickly with excellent yields and VO-6AP-MCM-41 shows high catalytic activity compared to Ni-6AP-MCM-41.

Mechanisms of methane decomposition and carbon species oxidation on the Pr0.42Sr0.6Co0.2Fe0.7Nb0.1O3−σ electrode with high catalytic activity

2015 ◽  
Vol 3 (45) ◽  
pp. 22816-22823 ◽  
Author(s):  
Peng Zhang ◽  
Guoqing Guan ◽  
Deni S. Khaerudini ◽  
Xiaogang Hao ◽  
Chunfeng Xue ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Carbon Deposition ◽  
Methane Decomposition ◽  
High Catalytic Activity ◽  
Carbon Species

Carbon deposition characteristics on PSCFN and Ni–YSZ due to thermal CH4 decomposition are investigated by using TPR technique.

scholarly journals Bio-Derived Catalysts: A Current Trend of Catalysts Used in Biodiesel Production

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 812
Author(s):  
Hoang Chinh Nguyen ◽  
My-Linh Nguyen ◽  
Chia-Hung Su ◽  
Hwai Chyuan Ong ◽  
Horng-Yi Juan ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Fossil Fuels ◽  
Current Trend ◽  
Biodiesel Production ◽  
High Catalytic Activity ◽  
Promising Alternative ◽  
Advantages And Disadvantages ◽  
Biodiesel Synthesis ◽  
Alkali Catalysts ◽  
A Current

Biodiesel is a promising alternative to fossil fuels and mainly produced from oils/fat through the (trans)esterification process. To enhance the reaction efficiency and simplify the production process, various catalysts have been introduced for biodiesel synthesis. Recently, the use of bio-derived catalysts has attracted more interest due to their high catalytic activity and ecofriendly properties. These catalysts include alkali catalysts, acid catalysts, and enzymes (biocatalysts), which are (bio)synthesized from various natural sources. This review summarizes the latest findings on these bio-derived catalysts, as well as their source and catalytic activity. The advantages and disadvantages of these catalysts are also discussed. These bio-based catalysts show a promising future and can be further used as a renewable catalyst for sustainable biodiesel production.

scholarly journals ZnCDs/ZnO@ZIF-8 Zeolite Composites for the Photocatalytic Degradation of Tetracycline

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 934
Author(s):  
Yong Cheng ◽  
Xiuxiu Wang ◽  
Yu Mei ◽  
Dan Wang ◽  
Changchun Ji
Keyword(s):  
Catalytic Activity ◽  
Photocatalytic Degradation ◽  
Photocatalytic Performance ◽  
Active Species ◽  
Degradation Efficiency ◽  
Experimental Result ◽  
Porous Nanostructure ◽  
Resultant Material

Considering the photocatalytic performance of CDs, ZnO, and the unique porous nanostructure and stability of ZIF-8, we prepared ZnCDs/ZnO@ZIF-8 zeolite composites. The resultant material represented an enhanced ability for the photodegradation of TC compared with that of ZnCDs and ZnO. The photocatalytic degradation efficiency reached over 85%. The catalytic activity of the composites was maintained after four cycles. The experimental result indicated that ×O2 radical was the active species in the reaction.

Sign in / Sign up

Export Citation Format

Share Document