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91.
Storage-Reduction of NOx over Combined Catalysts of Pt/Ba/Al2O3-Mn/Ba/Al2O3: Carbon Monoxide as Reductant
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Sha Deng Xuehui Li Jianhua Xiao Furong Wang Lefu Wang 《天然气化学杂志》2007,16(2):213-216
Storage-reduction of NOx by carbon monoxide was investigated over combined catalysts of Mn/Ba/Al2O3-Pt/Ba/Al2O3. Combination of Mn/Ba/Al2O3 and Pt/Ba/Al2O3 catalysts in different ways showed excellent NOx storage-reduction performance and the content of Pt could be reduced by 50%. Not only the addition of 5Mn/15Ba/Al2O3 to lPt/15Ba/Al2O3 could improve its storage ability, but also enhance the NOx conversion consequently. NOx conversion over the combined catalysts (the combined catalysts I and II) was increased under dynamic lean-rich burn conditions, the maximum NOx conversion increased from 69.4% to respectively 78.8% and 75.7% over two combined catalysts. 相似文献
92.
A convenient synthetic approach is established to prepare a new class of 1-l-α-amino acid derivatives of phospholene oxides by amination of (±)-1-chloro-2-phospholene-1-oxides with several optically pure l-α-amino acid esters. All compounds obtained as a diastereomeric mixture in good to high yields. The two diastereomers were successfully separated by column chromatography and structurally identified by their spectral analyses. 相似文献
93.
G. A. Vorob'eva S. D. Chemerisov A. V. Kozintsev Ya. S. Lebedev 《Russian Chemical Bulletin》1997,46(2):284-288
A new simple method was developed for the preparation of organometallic bi- and triradicals by the heterogeneous reaction
of γ-Al2O3 or analogous oxides with free radicals generated in solution through the interaction of 3,6-di-tert-butyl-o-benzoquinone with 3,6-di-tert-butylpyrocatechol. An explanation was offered for the plus sign of the dipoledipole coupling constant observed previously
in the ESR spectra recorded in a superstrong field at low temperatures.
Deceased.
Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 2, pp. 298–302, February, 1997. 相似文献
94.
95.
G. S. Zakharova L. Yu. Buldakova V. L. Volkov L. S. Molochnikov E. G. Kovaleva 《Russian Journal of Electrochemistry》2006,42(1):53-58
Complex vanadium and titanium oxides modified by copper ions are studied by the electrochemical and ESR methods. Oxides Cu x V2?y Ti y O5?δ·nH2O (0<y<1.33) have a layered structure and oxides Cu x Ti1?y V y O5+δ·nH2O (0<y<0.25), an anatase structure. The intercalation of cations Cu2+ into the hydrates leads to oxidation of V4+. According to ESR data, V4+ exists in the oxides in the form of VO2+ and an octahedral surround of oxygen (V4+?O6), respectively. The electroreduction of ions of d-elements and chemisorbed oxygen in the oxides is analyzed. The intercalation of cations Cu2+ alters the content of V4+ and the chemisorption ability of the oxides. Possible reasons for this phenomenon are discussed. 相似文献
96.
97.
In the Claus process hydrogen sulfide reacts to elemental sulfur. Because the Claus reaction is thermodynamically limited, sulfur compounds are still present in Claus tailgas. To avoid air pollution, the tailgas has to be treated.Alfa- and gamma-alumina are being used either as a catalyst or as a support for an active component in the Claus process and some tailgas treatment processes. In order to elucidate the mechanism of the Claus reaction, the adsorption of sulfur dioxide on both of the above aluminas was investigated using Fourier transform infrared spectroscopy.Different adsorbed species displaying a different heat of adsorption were detected. A broad band near 3500 cm–1 is associated with the basic hydroxyl groups. This band is assigned to a hydrogen bond between the surface of alumina and a bisulfite species. As bisulfite species are reactive towards hydrogen sulfide, we assume that bisulfite species are active intermediates on alumina in the Claus reaction. 相似文献
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99.
Maria Grazia Bonicelli Gianfranco Ceccaroni Franco Gauzzi Giuseppe Mariano 《Thermochimica Acta》2005,430(1-2):95-99
Differential scanning calorimetry (DSC) and particle size measurements were carried out on disproportionation products of pure SnO to investigate the fusion and solidification behaviour of Sn droplets and their catalytic nucleation on Sn oxides. If disproportionation reaction takes place at T ≥ 798 K, the products are metallic Sn and SnO2; but for 523 < T < 798 K, SnO2 is replaced by an intermediate oxide (IO) SnxO(1+x). On melting, samples with IO show a drop of melting point of metallic tin due to Gibbs–Thomson effect; no lowering of melting point was observed in samples with SnO2. On the other hand, if solidification occurs in the presence of IO, Tin droplets always displayed three distinct exothermic solidification peaks, but if it takes place in the presence of SnO2, only one exothermic peak is observed. Undercooling values and contact angles were determined for each of the heterogeneous nucleation processes. The different behaviour of metallic Tin droplets was related to the different lattice symmetry of SnO2 and IO, which act as nucleation catalysts. 相似文献
100.