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61.
A spatially resolved infrared (IR) imaging technique to monitor the linear adsorbed CO coverage on supported catalyst surface combining an IR bandpass filter and an IR thermography camera has been developed. Images acquired during the CO adsorption/desorption and ignition indicate that the technique provides an excellent method to image the change of surface coverage with a spatial resolution. It is expected that the combination of infrared thermography with spatially resolved imaging of surface coverage will provide a deeper insight in the dynamics of spatio-temporal patterns on heterogeneous catalysts. 相似文献
62.
The interactions of VOHPO4· 0.5H2O and (VO)2P2O7 with the ammoxidation feed and the single components such as ammonia, oxygen, water and component mixtures were studied in detail using XRD and temperature-programmed reaction spectroscopy. The aim of this work was to improve the knowledge of the formation of the active phases or active sites of the catalysts from their precursors under the condition of the ammoxidation reaction. Similar catalytic properties of various applied VPO materials were discussed in terms of the presence of similar structure elements (domains of adjacent edge-sharing VO6 octahedra-units and P-O-NH4 groups). 相似文献
63.
形态学边缘检测的新算法及其应用 总被引:3,自引:0,他引:3
刘岚岚 《红外与毫米波学报》1998,17(5):386-390
提出了一种基于数学形态学的边缘检测的所算法,该算法具有简便和灵活可编程控制等优点,比原来主算法更国完善,在实际应用中有着很好的前景,并给出了实验结果。 相似文献
64.
Zakaria Chajar Michel Primet Hélène Praliaud Michèle Chevrier Catherine Gauthier Frédéric Mathis 《Catalysis Letters》1994,28(1):33-40
The role of nitrogen dioxide in the selective reduction of NO by propane over a Cu-MFI zeolite is investigated. NO2 and NO reductions were carried out under similar conditions of reaction. In the presence of oxygen, the reduction of NO by C3H8 does not differ significantly from that of NO2. In the absence of oxygen, the reduction of NO2 by propane occurs with a partial decomposition of the nitric dioxide molecule. Such a decomposition leads to the formation of oxygen, which is responsible for the increase in catalytic activity by comparison with the same reaction performed with NO. NO2 formed and released in the gas phase during the reduction of NO by propane in the presence of oxygen does not play a predominant role in the catalytic process. 相似文献
65.
An algorithm for reconstructing a binary array of size N sx N from its forest of quadtree representation is presented. The algorithm traverses each tree of the forest in preorder and maps each ‘black’ node into the spatial domain. The time complexity in mapping is O(log N × Bn + Bp), where Bn is the number of black nodes in the forest and Bp is the number of black pixels in the N × N array. The algorithm has been implemented on an Apple II. 相似文献
66.
The partial oxidation of methane over the supported Rh (0.8 wt.%) catalysts was investigated. Two kinds of supports were used, MgO and Ti-modified MgO (prepared by grafting technique). Among the Ti-modified MgO supports, two different compounds were used as source of Ti: inorganic (chloride) and organic (alkoxide). The catalytic performance of Rh-supported catalysts depends on the support and varies in the sequence: Ti-MgO/I > Ti-MgO/O > MgO. Ti-containing catalysts exhibited higher activity and selectivity compared to MgO, which is especially noticeable at low temperature. Possible explanations for the phenomena observed were proposed on the basis of characterization results. 相似文献
67.
FTIR spectra of CO adsorbed on Pt/KL catalysts show that the relative band intensities and the total dispersion markedly depend on the catalyst preparation method (ion exchange, incipient wetness impregnation or co-impregnation with KCl). The CO stretching frequency of the dominant band for linear CO is shifted to higher wavenumbers, parallel with the proton concentration in the reduced catalyst, which is derived independently from the intensity of the IR bands of the OH groups. The results are in accordance with the model that electron-deficient platinum particles are platinum-proton adducts.On leave from: N.D. Zelinsky Institute of Organic Chemistry, Academy of Sciences, Moscow, USSR. 相似文献
68.
Michael W. Anderson 《Topics in Catalysis》1996,3(1-2):195-220
The power of solid-state NMR for the interrogation of porous catalytic materials is illustrated using three examples. First,
for the investigation of catalytic processes occurring within the confines of a microporous catalyst NMR is shown to reveal
both the details of shape-selectivity and the nature of internal surface species. Second, NMR is shown to be a powerful short-range
tool to reveal precise structural information on highly disordered microporous titanosilicates. Despite long-range disorder
the short-range order is maintained and can be easily studied. Finally, the same utility of probing short-range chemical phenomena
is shown to be crucial for the investigation of novel-ordered-amorphous-mesoporous materials known generically as M41S. This
class of material is currently one of the most important with potential catalytic application. 相似文献
69.
制备轻油蒸汽转化制氢镍催化剂新的共浸法 总被引:2,自引:0,他引:2
用一种新的共浸法制备一批轻油蒸汽转化催化剂样品。运用TG、DTG、DSC和XRD进行的研究发现,与一般共浸法相比,这种着重提高组份间相互作用的新制法有利于提高镍催化剂的活性、抗积炭性、稳定性和金属镍的分散度,并发现用新法制备的催化剂样品,在水热初期约30小时的过程中,出现了镍晶粒先聚集再分散的新现象。 相似文献
70.
Cu ion co-ordination-location in zeolites of MFI, erionite, mordenite matrices has been determined and the activity of the individual Cu sites compared for NO decomposition and its selective reduction by hydrocarbons or ammonia. It appears that Cu ions in the vicinity of one framework Al (site II), able to form stable Cu+-dinitrosyl complexes, and abundant in MFI structure, are responsible for high activity in NO decomposition. The Cu ions neighbouring two framework Al atoms (site I), and forming mostly mononitrosyl complexes, which dominate in erionite structure, provide a high activity in selective reduction of NO. 相似文献