Search results for "NOX"
showing 10 items of 727 documents
Palladium-Catalyzed Hydroxycarbonylation of Aryl and Vinyl Bromides by Mixed Acetic Formic Anhydride
2006
The palladium-catalyzed hydroxycarbonylation of aryl and vinyl bromides in the presence of acetic anhydride and lithium formate as a carbon monoxide source has been developed. The combination of palladium(II) acetate with 1,1'-bis(diphenylphosphino)ferrocene (dppf) is an efficient catalytic system when the reaction is carried out at 120 °C.
High affinity of "arbor" iron porphyrins for dioxygen
1998
International audience; The equilibrium rates of dioxygen and carbon monoxide binding have been measured for a series of capped iron porphyrins called "arbor". The affinity for dioxygen of these models is 100-fold higher than the highest previously reported values.
Nitric oxide metabolites (nitrite and nitrate) in several clinical condition.
2013
We determined the concentration of nitric oxide metabolites (NO2-+NO3-), expressed as NOx, in several clinical conditions. Regarding this, we have examined 25 subjects with arterial hypertension, 41 subjects with chronic kidney disease in conservative treatment, 106 subjects with metabolic syndrome subdivided according to the presence (n = 43) or not (n = 63) of diabetes mellitus, 48 subjects with obstructive sleep apnea syndrome (OSAS), 14 women with systemic sclerosis complicated with Raynaud's phenomenon, 42 dialyzed subjects and 105 young subjects with acute myocardial infarction (AMI). In subjects with arterial hypertension, chronic kidney disease, metabolic syndrome, systemic sclerosi…
First Synthesis of β-Keto Sulfoxides by a Palladium-Catalyzed Carbonylative Suzuki Reaction
2005
[reaction: see text] An unprecedented palladium-catalyzed three-component cross-coupling reaction between alpha-bromo sulfoxide, carbon monoxide, and aromatic boronic acids provides a new and efficient approach to the synthesis of beta-ketosulfoxides. The reaction takes place under mild conditions with a wide range of variously substituted aryl and heteroaryl boronic acids. The carbonylative cross-coupling reaction is strongly favored over competing direct cross-coupling and homocoupling processes, except with boronic acids carrying strong electron-withdrawing substituents.
Fe-doped Beta zeolite from organotemplate-free synthesis for NH3-SCR of NOx
2016
Two types of Beta zeolites, one from organotemplate-free synthesis with a Si/Al ratio of 9 and the other from a commercial one with a Si/Al ratio of 19, were employed here to dope Fe for NH3-SCR of NOx. Fe-Beta (Si/Al = 9) exhibits much higher activity than Fe-Beta (Si/Al = 19), especially at low-temperature regions (<250 °C). In addition, it also exhibits better hydrothermal stability as compared with Fe-Beta (Si/Al = 19), which demonstrates that it is a promising SCR catalyst with good activity as well as hydrothermal stability. The correlation between the quantitative calculation of the content of isolated Fe3+ in Beta zeolites and the NO conversion rate at 150 °C shows a linear relation…
Improvement of catalytic activity over Cu--Fe modified Al-rich Beta catalyst for the selective catalytic reduction of NOx with NH3
2016
Copper and iron bimetal modified Al-rich Beta zeolites from template-free synthesis were prepared for selective catalytic reduction (SCR) of NOx with NH3 in exhaust gas streams. Comparing to the Cu-based and Fe-based mono-component Beta catalysts, Cu(3.0)-Fe(1.3)-Beta bi-component catalyst shows better low-temperature activity and wider reaction-temperature window. Over 80% of NO conversion can be achieved at the temperature region of 125–500 °C. Due to the synergistic effect of copper and iron evidenced by XRD, UV–Vis–NIR, EPR and XPS measurements, the dispersion state of active components as well as the ratio of Cu2+/Cu+ and Fe3+/Fe2+ were improved over Cu(3.0)-Fe(1.3)-Beta. Isolated Cu2+…
Pumice-Supported Nickel Catalysts
1997
A series of nickel catalysts supported on pumice was prepared by precipitation and impregnation techniques. The influence of the calcination and reduction temperatures on the structural properties such as lattice parameters and particle dimensions of the oxide precursors and of the reduced catalysts was investigated by X-ray diffraction measurements. The effect of structural changes on the catalytic activity in the hydrogenation of carbon monoxide has been evaluated. The turnover frequencies, as well as product distributions, are discussed in terms of the influence of the support properties and of its interaction with the metal. Changes of the C2+yield over CH4yield ratio versus nickel disp…
Surface Study of Pumice Supported Nickel Catalysts Used in the Hydrogenation of CO
1998
A series of pumice supported nickel catalysts used in the CO hydrogenation reaction were characterised by X-ray photoelectron spectroscopy. Qualitative and quantitative analysis of the XPS peaks have shown the effect of the calcination conditions on the chemical state of the nickel before hydrogenation and the particle size of the metal after reduction. Calcination at high temperature determined enrichment of sodium ions on the surface of the support and also on the metal particles. After exposure to the gas mixture CO/H2, formation of nickel carbides and other carbon species was checked. The correlation found between the surface atomic ratio Na/Si and the activity and selectivity of the ca…
NOx selective catalytic reduction at high temperatures with mixed oxides derived from layered double hydroxides
2012
[EN] Mixed oxides derived from layered double hydroxides (LDHs) have been investigated as potential catalysts for the NOx removal at high temperatures. The best results were obtained with Co–Al mixed oxides derived from LDHs that are active at 750 ◦C in the presence of oxygen and water. These catalysts could reduce or/and decompose the NOx formed in the dense phase of the FCC regenerator, being deactivated at oxygen concentrations higher than 1.5%. Nevertheless this deactivation is not permanent and they would be regenerated after reduction with hydrogen at 530 ◦C. The influence of the layered double hydroxides (LDHs) preparation method on the catalyst activity was studied, observing that t…
Tailoring polymers through interplay of ligands within precatalysts: 8-(Nitro/benzhydryl-arylimino)-7,7-dimethyl-5,6-dihydroquinolylnickel halides in…
2017
A series of 8-(nitro/benzhydryl-substituted arylimino)-7,7-dimethyl-5,6-dihydroquinolines and the corresponding nickel halide complexes were synthesized and characterized. Molecular structures of representative nickel complexes were determined by single crystal X-ray diffraction, showing the dinuclear dimers with distorted square-pyramidal geometry around the nickel center. The binding energies determined by X-ray photoelectron spectroscopy (XPS) indicate the effective coordination between the sp2-nitrogen and nickel atoms as well as the influence of both the halogen ligands and the substituents within dihydroquinolines on the strength of the NiN bond. Ethylene polymerization with the nicke…