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1.
Exchange and oxidation of C16O were investigated at 450°C on 18O-predosed Rh and Pt catalysts supported on A12O3, CeO2 and CeO2-Al2O3. In all cases, a rapid exchange of C16O with the surface can be observed. CO oxidation leads to C16O2, C16O18O and C18O2. Significant formation of C16O2 is due to the relatively high 16O coverage in reaction resulting from the C16O exchange and from an exchange between O surface species and 16O internal atoms. Hydrogen is also formed via a water-gas shift reaction (CO + surface OH) in higher proportion on CeO2-containing catalysts than on A12O3. Chlorine inhibits all the reactions (exchange, oxidation and WGS) and particularly the internal exchange. 相似文献
2.
Tony Maillet Jacques Barbier Jr. Daniel Duprez 《Applied catalysis. B, Environmental》1996,9(1-4):251-266
A 1% Pd catalyst (38% dispersion) was prepared by impregnating a γ-alumina with palladium acetylacetonate dissolved in acetone. The behaviour of this catalyst in oxidation and steam reforming (SR) of propane was investigated. Temperature-programmed reactions of C3H8 with O2 or with O2 + H2O were carried out with different stoichiometric ratios S(S =[O2]/5[C3H8]). The conversion profiles of C3H8 for the reaction carried out in substoichiometry of O2 (S < 1) showed two discrete domains of conversion: oxidation at temperatures below 350°C and SR at temperatures above 350°C. The presence of steam in the inlet gases is not necessary for SR to occur: there is sufficient water produced in the oxidation to form H2 and carbon oxides by this reaction. Contrary to what was observed with Pt, an apparent deactivation between 310 and 385°C could be observed with Pd in oxidation. This is due to a reduction of PdOx into Pd0, which is much less active than the oxide in propane oxidation. Steam added to the reactants inhibits oxidation while it prevents the reduction of PdOx into Pd0. Compared to Pt and to Rh, Pd has a higher thermal resistance: no deactivation occurred after treatment up to 700°C and limited deactivation after treatment up to 900°C, provided that the catalyst is maintained in an oxygen-rich atmosphere during the cooling. 相似文献
3.
PtRh catalysts were prepared by coimpregnation, with chlorine-free precursors of a -alumina. They were sintered at 973 K under a continuous flow of O2 (1% in Ar or air) or of a flow of Ar into which pulses of O2 were injected periodically. Under the latter conditions the sintering was significantly accelerated, particularly for a certain value of the period of O2 pulses. 相似文献
4.
S. Royer C. Ayrault C. Carnevillier F. Epron P. Marcot D. Duprez 《Catalysis Today》2006,117(4):543-548
Oxidation activity and stability under reaction was investigated for a series of mixed oxide catalysts, doped or not by a precious metal (Pd, Pt). The reaction feedstock, containing CO, H2, CH4, CO2 and H2O, simulated gases issued from H2 production processes for fuel cells. Contrarily to conventional noble metal catalysts, mixed oxide samples present generally good stability under reaction at high temperature. The activities measured for the perovskite and hexaaluminate catalysts, are however largely lower than that of the reference Pd/Al2O3 catalyst. High activities were obtained after impregnation of 1.1 wt.% Pd or 0.8 wt.% Pt on the hexaaluminates samples. Even if Pd/Al2O3 was found to present a high activity, this sample suffered from drastic deactivation at 700 °C. Better stability were obtained on perovskite. Furthermore, doping hexaaluminate by Pt led to samples with good activities and high stability. Even if better activities were obtained by doping the hexaaluminate samples by Pd, the Pd/BaAl12O19 strongly deactivated, as it was previously observed for the reference catalyst. Interestingly, this Pd deactivation was not observed when Pd was impregnated on the Mn substituted hexaaluminate, leading to a stable and active catalyst. This suggests that it is possible to stabilize the palladium in its oxidized form at high temperature (700 °C) on the surface of some supports. 相似文献
5.
Sanaa Elbouazzaoui Xavier Courtois Patrice Marecot Daniel Duprez 《Topics in Catalysis》2004,(1):493-496
The deactivation of a Pt/Ba/Al2O3 NO
x
-trap model catalyst submitted to SO2 treatment and/or thermal ageing at 800 °C was studied by H2 temperature programmed reduction (TPR), X-ray diffraction (XRD) and NO
x
storage capacity measurements.The X-ray diffractogram of the fresh sample exhibits peaks characteristic for barium carbonate. Thermal ageing leads to the decomposition of barium carbonate and to the formation of BaAl2O4. The TPR profile of the sulphated sample shows the presence of (i) surface aluminium sulphates, (ii) surface barium sulphates, (iii) bulk barium sulphates. The exposure to SO2 after ageing leads to a small decrease of the surface barium-based sulphates, expected mainly as aluminate barium sulphates. This evolution can be attributed to a sintering of the storage material. TPR experiments also show that thermal treatment at 800 °C after the exposure to SO2 involves the decomposition of aluminium surface sulphates to give mainly bulk barium sulphates, also pointed out by XRD. Thus, the thermal treatment at 800 °C leads to a stabilization of the sulphates.These results are in accordance with the NO
x
storage capacity measurements. On non-sulphated catalysts, the treatment at 800 °C induces to a decrease of the NO
x
storage capacity, showing that barium aluminate presents a lower NO
x
storage capacity than barium carbonate. Sulphation strongly decreases the NO
x
storage capacity of catalysts, whatever the initial thermal treatment, showing that barium sulphates inhibit the NO2 adsorption. Moreover, the platinum activity for the NO to NO2 oxidation is lowered by thermal treatments. 相似文献
6.
The effect of hydrogen pressure (pH2) and temperature (T) was investigated on the hydrogenolytic ring opening of methylcyclopentane (MCP) over silica and alumina supported rhodium catalysts. Strong dependence could be seen in the activity and in distribution of ring opening products as a function of reaction conditions. Temperature and hydrogen pressure did not affect the position of the first C–C bond rupture. However, the final ring opening product distribution was largely influenced by the reaction conditions due to the different ability of intermediates to undergo further hydrogenolysis. 相似文献
7.
A Scalable Architecture for MPEG-4 Wavelet Quantization 总被引:3,自引:0,他引:3
Bart Vanhoof Mercedes Peón Gauthier Lafruit Jan Bormans Lode Nachtergaele Ivo Bolsens 《The Journal of VLSI Signal Processing》1999,23(1):93-107
Wavelet-based image compression has been adopted in MPEG-4 for visual texture coding. All wavelet quantization schemes in MPEG-4—Single Quantization (SQ), Multiple Quantization (MQ) and Bi-level Quantization—use Embedded Zero Tree (EZT) coding followed by an adaptive arithmetic coder for the compression and quantization of a wavelet image. This paper presents the OZONE chip, a dedicated hardware coprocessor for EZT and arithmetic coding. Realized in a 0.5 m CMOS technology and operating at 32 MHz, the EZT coder is capable of processing up to 25.6 Mega pixel-bitplanes per second. This is equivalent to the lossless compression of 31.6 8-bit grayscale CIF images (352 × 288) per second. The adaptive arithmetic coder processes up to 10 Mbit per second. The combination of the performance of the EZT coder and the arithmetic coder allows the OZONE to perform visual-lossless compression of more than 30 CIF images per second. Due to its novel and scalable architecture, parallel operation of multiple OZONEs is supported. The OZONE functionality is demonstrated on a PC-based compression system. 相似文献
8.
Erläuterung der Methoden zur Ermittlung mechanischer Spannungen unter besonderer Berücksichtigung der räumlichen Verhältnisse bei der Röntgenmessung. Darstellung der Verformungsgeometrie und der daraus abgeleiteten Meßverfahren. Vergleichende Gegenüberstellung des Röntgen-φ-Integralverfahrens mit dem Röntgen-ψ-Integralverfahren. 相似文献
9.
10.
Henriette Bretschneider Mandy Quade Anja Lode Michael Gelinsky Stefan Rammelt Corina Vater 《International journal of molecular sciences》2021,22(11)
To develop cost-effective and efficient bone substitutes for improved regeneration of bone defects, heparin-modified mineralized collagen scaffolds were functionalized with concentrated, naturally occurring bioactive factor mixtures derived from adipose tissue, platelet-rich plasma and conditioned medium from a hypoxia-treated human bone marrow-derived mesenchymal stem cell line. Besides the analysis of the release kinetics of functionalized scaffolds, the bioactivity of the released bioactive factors was tested with regard to chemotaxis and angiogenic tube formation. Additionally, functionalized scaffolds were seeded with human bone marrow-derived mesenchymal stromal cells (hBM-MSC) and their osteogenic and angiogenic potential was investigated. The release of bioactive factors from the scaffolds was highest within the first 3 days. Bioactivity of the released factors could be confirmed for all bioactive factor mixtures by successful chemoattraction of hBM-MSC in a transwell assay as well as by the formation of prevascular structures in a 2D co-culture system of hBM-MSC and human umbilical vein endothelial cells. The cells seeded directly onto the functionalized scaffolds were able to express osteogenic markers and form tubular networks. In conclusion, heparin-modified mineralized collagen scaffolds could be successfully functionalized with naturally occurring bioactive factor mixtures promoting cell migration and vascularization. 相似文献