scholarly journals Low Temperature Oxidation of Carbon Monoxide over Mesoporous Au-Fe2O3Catalysts

2017 ◽  
Vol 2017 ◽  
pp. 1-14 ◽  
Author(s):  
Abdulmohsen Ali Alshehri ◽  
Katabathini Narasimharao

Low temperature active and stable mesoporous Au (0.1, 0.2, 0.5, and 1.0 wt.%) supportedα-Fe2O3catalysts were prepared via deposition-precipitation method. The H2-pretreated catalyst with 0.5 wt.% Au loading offered CO conversion of 100% at 323 K and showed continual activity for at least 120 h. X-ray diffraction and transmission electron microscopy analysis indicate that Au species were highly dispersed as nanoparticles (20–40 nm) on the surface ofα-Fe2O3support even after thermal treatment at 773 K. The N2-physisorption measurements show that the synthesizedα-Fe2O3support and Au-Fe2O3nanocomposites possessed mesopores with high specific surface area of about 158 m2 g−1. X-ray photoelectron spectroscopy and H2-TPR results reveal that the Au species exist in metallic and partially oxidized state due to strong interaction with the support. Effective Au-Fe2O3interaction resulted in a high activity for Au nanoparticles, locally generated by the thermal treatment at 773 K in air.

2009 ◽  
Vol 08 (03) ◽  
pp. 281-283 ◽  
Author(s):  
MASOUD SALAVATI-NIASARI ◽  
FATEMEH DAVAR

Mn3O4 nanocrystals have been prepared using [bis(2-hydroxyacetophenato)manganese(II)] as precursor. Transmission electron microscopy analysis demonstrated nanocrystals Mn3O4 with an average diameter of about 20 nm. The structural study by X-ray diffraction indicates that these nanocrystals have pure tetragonal phase. The phase pure samples were characterized using X-ray Photoelectron Spectroscopy for Mn 2p level. The values of binding energies are consistent with the relative values reported in the literature.


Processes ◽  
2020 ◽  
Vol 8 (8) ◽  
pp. 926
Author(s):  
Shamim Ahmed Hira ◽  
Mohammad Yusuf ◽  
Dicky Annas ◽  
Hu Shi Hui ◽  
Kang Hyun Park

Activated carbon (AC) was fabricated from carrot waste using ZnCl2 as the activating agent and calcined at 700 °C for 2 h in a tube furnace. The as-synthesized AC was characterized using Fourier-transform infrared spectroscopy, X-ray diffraction analysis, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller analysis; the results revealed that it exhibited a high specific surface area and high porosity. Moreover, this material displayed superior catalytic activity for the degradation of toxic Rhodamine B (RhB) dye. Rate constant for the degradation of RhB was ascertained at different experimental conditions. Lastly, we used the Arrhenius equation and determined that the activation energy for the decomposition of RhB using AC was approximately 35.9 kJ mol−1, which was very low. Hopefully it will create a great platform for the degradation of other toxic dye in near future.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 202
Author(s):  
Long Lu ◽  
Xueman Wang ◽  
Chunhua Hu ◽  
Ying Liu ◽  
Xiongbo Chen ◽  
...  

Nanosized V-Ce oxides supported on TiO2 (VCT) were prepared and utilized in the low-temperature selective catalytic reduction (SCR) of NO with NH3. Compared with the other V-Ce oxides-based catalysts supported on Al2O3, ZrO2, and ZSM-5, VCT showed the best SCR activity in a low-temperature range. The NOx conversion of 90% could be achieved at 220 °C. Characterizations including X-ray diffraction (XRD), scanning election micrograph (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption with NH3 (NH3-TPD), and temperature-programmed reduction with H2 (H2-TPR) showed that V1.05Ce1/TiO2 exhibited a good dispersion of V2O5, enrichment of surface Ce3+ and chemical-absorbed oxygen, and excellent redox capacity and acidity, which resulted in the best SCR performance at low temperature.


Metals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1307
Author(s):  
Oscar Hernández ◽  
Claudio Aguilar ◽  
Ariosto Medina

Mechanical Alloying (MA) has the ability to extend the solubility limits of immiscible alloys in a solid state. In this work, a Cu-10 wt% Mo alloy was synthesized by mechanical alloying, using a high-energy mill type SPEX. The X-ray diffraction and Rietveld results show a crystallite size of 24 and 22 nm of Cu and Mo, respectively, with an occupation value of Mo inside the Cu structure of 27%, which was identificated by Energy Dispersive X-ray Spectroscopy and High-Resolution Transmission Electron Microscopy analysis. After that, the alloy was sinterized in an oven, heating the alloy to 1000 °C—close to the melting point of Cu (1085 °C). Electrochemical tests were carried out under a saline environment of synthetic seawater. The results show that the polarization curve of the alloy showed a pitting corrosion at about 134.83 mV, as well as a repasivation phenomenon (Erp = 241.47 mV) in the cathodic branch. Finally, three time constants were observed in the Nyquist diagrams: formation of a corrosion product film, load transfer, and diffusion, indicating that the corrosion properties in this alloy were improved compared with other Cu–alloys.


2011 ◽  
Vol 77 (16) ◽  
pp. 5584-5590 ◽  
Author(s):  
Liang Shi ◽  
Sara M. Belchik ◽  
Andrew E. Plymale ◽  
Steve Heald ◽  
Alice C. Dohnalkova ◽  
...  

ABSTRACTShewanella oneidensisMR-1 possesses a periplasmic [NiFe]-hydrogenase (MR-1 [NiFe]-H2ase) that has been implicated in H2production and oxidation as well as technetium [Tc(VII)] reduction. To characterize the roles of MR-1 [NiFe]-H2ase in these proposed reactions, the genes encoding both subunits of MR-1 [NiFe]-H2ase were cloned and then expressed in an MR-1 mutant withouthyaBandhydAgenes. Expression of recombinant MR-1 [NiFe]-H2ase intransrestored the mutant's ability to produce H2at 37% of that for the wild type. Following purification, MR-1 [NiFe]-H2ase coupled H2oxidation to reduction of Tc(VII)O4−and methyl viologen. Change of the buffers used affected MR-1 [NiFe]-H2ase-mediated reduction of Tc(VII)O4−but not methyl viologen. Under the conditions tested, all Tc(VII)O4−used was reduced in Tris buffer, while in HEPES buffer, only 20% of Tc(VII)O4−was reduced. The reduced products were soluble in Tris buffer but insoluble in HEPES buffer. Transmission electron microscopy analysis revealed that Tc precipitates reduced in HEPES buffer were aggregates of crystallites with diameters of ∼5 nm. Measurements with X-ray absorption near-edge spectroscopy revealed that the reduction products were a mixture of Tc(IV) and Tc(V) in Tris buffer but only Tc(IV) in HEPES buffer. Measurements with extended X-ray adsorption fine structure showed that while the Tc bonding environment in Tris buffer could not be determined, the Tc(IV) product in HEPES buffer was very similar to Tc(IV)O2·nH2O, which was also the product of Tc(VII)O4−reduction by MR-1 cells. These results shows for the first time that MR-1 [NiFe]-H2ase catalyzes Tc(VII)O4−reduction directly by coupling to H2oxidation.


2007 ◽  
Vol 280-283 ◽  
pp. 305-310
Author(s):  
Tao Yan ◽  
Xiao Lin Liu ◽  
Jian Feng Chen

The sensitivity of CuO dispersed on fluorite-type oxide, namely CeO2 was studied in this work. Mixed oxide sample of nanostructured CuxCe1-xO2-y of various composition were generated by step chemical precipitation method. Distinct copper species were identified as a function of copper content by X-ray photoelectron spectroscopy, X-ray powder diffraction, the special surface areas, transmission electron microscopy, scanning electron microscopy analysis, and sensing properties to CO. It was found that only small amounts of copper are sufficient to promote the sensitivity of CeO2 by several orders of magnitude, which excessive amounts of copper (Cu/(Cu+Ce)>0.12) are detrimental to the sensing properties of nanocompositions. The possible causes for this behavior are also discussed.


Sign in / Sign up

Export Citation Format

Share Document