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1.
氧化铈气凝胶担载氧化铜催化剂上的一氧化碳氧化   总被引:15,自引:1,他引:15  
 以一氧化碳氧化为探针反应,考察了氧化铈气凝胶担载氧化铜催化剂的催化活性,研究了催化剂中氧化铜的含量、载体及催化剂的焙烧温度对催化剂活性的影响.结果表明,氧化铈气凝胶担载的氧化铜催化剂对一氧化碳氧化反应呈现出高催化活性,适当温度下焙烧载体及催化剂有利于提高催化剂的催化活性;随着催化剂中氧化铜含量的增加,一氧化碳完全转化的温度降低,但当w(CuO)>12%时,过量的氧化铜以体相形式而不是以高分散形式存在,对催化剂活性的影响很小.  相似文献   

2.
A γ-alumina-supported copper-manganese oxide catalyst prepared by an impregnation method was used for DME synthesis from CO/H2 (syngas). The Cu-Mn/γ-Al2O3 catalyst exhibits high catalytic activity in CO hydrogenation. The effect of the loading amount of Cu, the ratio of n(Cu)/n(Mn) and the reaction conditions on the activity and selectivity to dimethyl ether (DME) from CO/H2 (syngas) were investigated. The activity was found to increase with increasing surface area of metallic copper to some extent, but it is not a linear relationship. This indicated that the catalytic activity depends on both the metallic copper area and the synergy between the copper and manganese oxide. This revised version was published online in June 2006 with corrections to the Cover Date.  相似文献   

3.
并流共沉淀法制备了CuO/ZnO/Al2O3催化剂前驱体及催化剂,用XRD、TG-DTG、TPR、N2吸附及加压微反活性评价技术,考察了母料老化时间对催化剂前驱体物相组成及焙烧后物料中CuO-ZnO间的作用和物化性能的影响,提出了催化剂母料物相随老化时间的变化。研究表明,老化时间对催化剂活性的影响是通过改变催化剂比表面积及形成CuO ZnO固溶体的结果。  相似文献   

4.
The catalytic conversion of methane and carbon dioxide was studied in a fluidized bed reactor supported by a 13.56?Hz driven coaxial DBD-reactor. Palladium or cupper catalyst which are covered on Al2O3 particles were used. The goal was to test whether biogas can be used for the production of synthesis gas. The influences of discharge power, catalysts and temperature of the catalyst bed on the product yield were studied. The starting material and product stream was analyzed by quadrupole mass spectrometry and infrared spectroscopy. H2/CO ratios can be adjusted in a range between 0.65 (without a catalyst) and 1.75 (using a copper catalyst). The process is highly selective for hydrogen production (up to 83%, using a Palladium catalyst). A copper catalyst increases the H2/CO ratio can from 1.04 to 1.16 and the palladium catalyst from 1.11 to 1.43 by heating the catalyst to a temperature of 250°C.  相似文献   

5.
湿混法制备甲醇氧化重整制氢CuZnAlZr催化剂   总被引:3,自引:1,他引:3  
用简易湿混法制备了用于甲醇氧化重整制氢的CuZnAlZr催化剂,与共沉淀法制备的催化剂比较,结果表明,湿混法制备的催化剂具有相当的中高温活性和略低的低温活性,有较高的CO2选择性。XRD、TPR、TG-DSC等表征结果显示,湿混法制备的催化剂中铜组分易于向表面迁移和富集,并可能与氧化铝作用生成铜铝复合氧化物,具有了更高的Cu分散度和Cu0比表面浓度。湿混法制备的催化剂对甲醇氧化重整反应有较好的稳定性,经100 h的连续反应,在275 ℃时甲醇转化率在90%以上,重整气中氢气体积分数大于60%,CO2选择性接近99%。  相似文献   

6.
自从ICI低压、低温甲醇合成过程取代高压过程以来,人们对该过程所使用的Cu/ZnO/Al_2O_3或Cu/ZnO/Cr_2O_3催化剂有极大的兴趣。Herman、Klier等人已证明这种低压、低温下的活性应归属于Cu-ZnO间的相互作用,在相同的条件下,单纯的铜或氧化锌的活性几乎可以忽略不计,而氧化铝或氧化铬主要起结构助剂的作用。由此可见,控制适宜的Cu-ZnO间的相互作用是提高甲醇合成活性的关键,因此,如何才能产生这种适宜的相互作用就成了人们极为重视的研究课题。到目前为止,人们普遍采用沉淀法制备铜基甲醇合成催化剂,试图通过改变各种制备条件来开发更好的  相似文献   

7.
将醋酸铜热解制备的Cu2O/AC(活性炭)催化剂,在氧化(O2/N2)和还原(H2/N2、CO/N2)气氛下进行预处理。350 ℃下预处理4 h,氧化气氛中Cu2O完全被氧化为CuO,还原气氛中Cu2O被还原为单质铜。经CO/N2预处理的催化剂表面Cu0分散性好,催化活性显著升高。在常压固定床微型反应装置上测试,在140 ℃的反应温度下,碳酸二甲酯的时空收率和选择性分别达到了261.9 mg/(g·h)和74.7%。反应后,还原气氛(H2/N2、CO/N2)预处理的催化剂与Cu2O/AC催化剂中铜物种价态组成趋于一致,催化活性亦趋于一致。关联反应前后催化剂表面铜物种的变化和催化活性的差异,可以认为Cu0具有较高的初始催化活性,Cu2O活性和价态均较为稳定,CuO活性较低。  相似文献   

8.
Carbon monoxide (CO) is a very poisonous gas present in the atmosphere. It has significant effects on human beings, animals, plants and the climate. Automobile vehicle exhaust contributes 64% of the CO pollution in urban areas. To control this exhaust pollution, various types of catalysts in catalytic converters have been investigated. Increasing costs of noble metals as a catalyst in automobile vehicles motivates the investigation of material that can be substituted for noble metals. Among the non-noble metals, copper (Cu) is found to be the most capable and highly active catalyst for CO oxidation, compared to precious metal catalysts. Lower cost, easy availability and advance preparation conditions with stabilizers, promoters and so on, make Cu a good choice as an auto exhaust purification catalyst. The oxidation of CO proceeds very quickly over Cu°, followed by Cu+ and Cu2+. The Cu2O catalyst is more active in an O2-rich atmosphere than in O2-lean conditions. The reduced species of copper (Cu0, Cu+) are essential for better CO oxidation but smaller Cu particles could be less active than the higher ones. There is a great deal of research available on the Cu catalyst for CO oxidation, but there is a gap in the literature for a review article individually applied to the Cu catalyst for CO oxidation. To fill this gap, the present review updates information on Cu catalysts in the purification of exhaust gases.  相似文献   

9.
过渡金属氧化物掺杂对铜锰氧化物催化CO氧化性能的影响   总被引:2,自引:0,他引:2  
以乙酸铜和乙酸锰为铜锰前驱体,以NH4HCO3为沉淀剂,相应金属硝酸盐为掺杂剂,采用共沉淀法制备了不同过渡金属氧化物掺杂的铜锰氧化物催化剂.?采用N2物理吸附、X射线衍射,氢气-程序升温还原和原位红外漫反射光谱等方法对催化剂进行了表征,考察了系列催化剂上CO反应性能.?结果表明,掺杂过渡金属氧化物可以调变催化剂对CO的吸附能力,进而影响催化剂性能.  相似文献   

10.
The characterization of La(Co,Cu)O3 perovskites has been performed by several techniques including XRD, BET, H2-TPR, O2-TPO, TPRS, and the solids tested as catalysts for the hydrogenation of CO. The reducibility of the perovskites is strongly affected by the preparation route, calcination temperature, catalyst morphology, and the amount of remnant alkali. Compared with the citrate-derived perovskite, LaCoO3 sample prepared by mechano-synthesis has various distinct Co3+ ions in perovskite lattice, which are reduced at different temperatures. Under typical conditions, the reduction of cobalt ions occurs in two consecutive steps: Co3+/Co2+ and Co2+/Co0, while the intra-lattice copper ions are directly reduced from Cu2+ to Cu0. The reducibility of cobalt ions is promoted by the presence of metallic copper, which is formed at a lower reduction temperature. The re-oxidation of the reduced lanthanum cobaltite perovskite could regenerate the original structure, whereas that of the reduced Co-Cu-based samples is less reversible under the same experimental conditions.The cobalt atom in the reduced perovskites plays an important role in the dissociation of CO, but the presence of a neighboring copper along with remnant sodium ions on the catalyst surface has remarkably affected the reactivity of cobalt for CO hydrogenation. The addition of copper into the perovskite framework leads to a change in the product distribution of CO hydrogenation and a decrease in reaction temperature. An increased copper content leads to a substantial decline in the rate of methanation and an increase in the formation of higher alcohols. A close proximity between cobalt and copper sites on the Na+-modified catalyst surface of the reduced nanocrystalline Co-Cu-based perovskites plays a crucial role in the synthesis of higher alcohols from syngas.  相似文献   

11.
研究了Cu、K助剂对共沉淀型FeMn/SiO2催化剂还原行为、吸附行为及费托(F-T)合成活性和选择性的影响. Cu助剂以与Fe、Mn、SiO2共沉淀的方式引入, 而K助剂是在喷雾干燥前均匀加入沉淀浆料引入的. 结果表明, Cu可明显提高催化剂的还原性能, K助剂能促进催化剂在CO中的还原但抑制在H2中的还原, 而同时加入Cu和K会进一步促进催化剂在H2或CO中的还原; Cu助剂能促进H2吸附而K助剂对H2吸附无明显影响; Cu在一定程度上提高了F-T合成活性, 缩短了反应诱导期, K明显促进了CO的转化而相对抑制了H2的转化, 并且延长了反应的诱导期, Cu与K协同作用不仅提高反应的转化率而且缩短了反应的诱导期; K使得烃产物平均分子量增加, Cu单独对烃产物分布影响不明显, 而与K共同作用会进一步增加烃产物的分子量.  相似文献   

12.
An efficient O-arylation of phenols and aliphatic alcohols with aryl halides was developed that uses an air-stable copper(I) complex as the catalyst. This arylation reaction can be performed in good yield in the absence of Cs2CO3. A variety of functional groups are compatible with these reaction conditions with low catalyst loading levels.  相似文献   

13.
采用原位合成法在γ-Al2O3表面合成了锌铝水滑石,再通过顺次浸渍法制备了一系列掺杂稀土改性的M(M=Y、La、Ce、Sm、Gd)/Cu/ZnAl催化材料,并将其应用于甲醇水蒸气重整制氢反应。探讨了稀土掺杂改性对Cu/ZnAl催化剂催化性能的影响,并采用XRD、SEM-EDS、BET、H2-TPR、XPS和N2O滴定等手段对催化剂进行了表征。结果表明,催化剂的活性与Cu比表面积和催化剂的还原性质密切相关,Cu比表面积越大,还原温度越低,催化活性越高。稀土Ce、Sm、Gd的引入能改善活性组分Cu的分散度、Cu比表面积以及催化剂的还原性质,进而提高催化剂的催化活性。其中,Ce/Cu/ZnAl催化剂表现出最佳的催化活性,在反应温度为250 ℃时,甲醇转化率达到100%,CO含量为0.39%,相比Cu/ZnAl催化剂,甲醇转化率提高了近40%。  相似文献   

14.
Zhang WZ  Li WJ  Zhang X  Zhou H  Lu XB 《Organic letters》2010,12(21):4748-4751
A highly selective synthesis of a variety of functionalized allylic 2-alkynoates was realized via the carboxylative coupling of terminal alkynes, allylic chlorides, and CO(2) catalyzed by the N-heterocyclic carbene copper(I) complex (IPr)CuCl. The catalyst can be easily recovered without any loss in activity and product selectivity.  相似文献   

15.
The La2CuO4 crystal nanofibers were prepared by using single-walled carbon nanotubes as templates under mild hydrothermal conditions. The steam reforming of methanol (SRM) to CO2 and H2 over such nanofiber catalysts was studied. At the low temperature of 150 °C and steam/methanol=1.3, methanol was completely (100%, 13.8 g/h g catalyst) converted to hydrogen and CO2 without the generation of CO. Within the 60 h catalyst lifespan test, methanol conversion was maintained at 98.6% (13.6 g/h g catalyst) and with 100% CO2 selectivity. In the meantime, for distinguishing the advantage of nanoscale catalyst, the La2CuO4 bulk powder was prepared and tested for the SRM reaction for comparison. Compared with the La2CuO4 nanofiber, the bulk powder La2CuO4 showed worse catalytic activity for the SRM reaction. The 100% conversion of methanol was achieved at the temperature of 400 °C, with the products being H2 and CO2 together with CO. The catalytic activity in terms of methanol conversion dropped to 88.7% (12.2 g/h g catalyst) in 60 h. The reduction temperature for nanofiber La2CuO4 was much lower than that for the La2CuO4 bulk powder. The nanofibers were of higher specific surface area (105.0 m2/g), metal copper area and copper dispersion. The in situ FTIR and EPR experiments were employed to study the catalysts and catalytic process. In the nanofiber catalyst, there were oxygen vacancies. H2-reduction resulted in the generation of trapped electrons [e] on the vacancy sites. Over the nanofiber catalyst, the intermediate H2CO/HCO was stable and was reformed to CO2 and H2 by steam rather than being decomposed directly to CO and H2. Over the bulk counterpart, apart from the direct decomposition of H2CO/HCO to CO and H2, the intermediate H2COO might go through two decomposition ways: H2COO=CO+H2O and H2COO=CO2+H2.  相似文献   

16.
《天然气化学杂志》2012,(4):374-380
In this work,experimental studies of biomass gasification under different operating conditions were carried out in an updraft gasifier combined with a copper slag reformer.The influence of gasification temperature,equivalence ratio(ER) and copper slag catalyst addition on gas production and tar yield were investigated.The experimental results showed that the content of H2 and CO,gas yield and LHV increased,while the tar yield and the content of CO2,CH4 and C2Hx in the gas product decreased with the temperature.At 800C,with the increase of ER,the LHV,the tar yield and the content of H2,CO,CH4 and C2Hx in gas products decreased,while the gas yield and the content of CO2 increased.Copper slag was introduced into the secondary reformer for tar decomposition.The Fe3O4 phase in the fresh copper slag was reduced to FeO(Fe2+) and metallic Fe by the gas product.Fe species(FeO and metallic Fe) acted as the active sites for tar catalytic decomposition.The catalytic temperature had a significant influence on tar conversion and the composition of the gas product.Typically,the tar conversion of about 17%-54% could be achieved when the catalytic temperature was varied from 750 to 950 C.Also,the content of H2 and CO increased with the catalytic temperature,while that of CO2,CH4 and C2Hx in the gas product decreased.It was demonstrated that copper slag was a good catalyst for upgrading the gas product from biomass gasification.  相似文献   

17.
氧化铈气凝胶担载氧化铜催化剂的TPR研究   总被引:8,自引:0,他引:8  
 采用程序升温还原研究了氧化铈气凝胶担载氧化铜催化剂的还原行为,并与其对一氧化碳氧化反应的催化活性进行了关联.发现此类催化剂中存在两种类型的氧化铜,即体相氧化铜和分散于载体表面的氧化铜,且后者中的部分氧化铜还原后易被氧化.随着此易被氧化的铜含量的增加,催化剂对一氧化碳氧化反应的催化活性升高,表明此种类型的铜为催化剂的活性组分.  相似文献   

18.
An improved procedure for the preparation of Re2(CO)10 is reported. Carbonylation of methanol solutions of NaReO4 (3200 psi, 230°C, 48 h) in the presence of a metallic copper catalyst affords Re2(CO)10 in 90% yield.  相似文献   

19.
Selective CO oxidation in a mixture simulating the methanol steam reforming product with an air admixture was studied over Ru/Al2O3 catalysts in a quasi-adiabatic reactor. On-line monitoring of the gas temperature in the catalyst bed and of the residual CO concentration at different reaction conditions made it possible to observe the ignition and quenching of the catalyst surface, including transitional regimes. A sharp decrease in the residual CO concentration takes place when the reaction passes to the ignition regime. The evolution of the temperature distribution in the catalyst bed in the ignition regime and the specific features of the steady-state and transitional regimes are considered, including the effect of the sample history. In selective CO oxidation and in H2 oxidation in the absence of CO, the catalyst is deactivated slowly because of ruthenium oxidation. In both reactions, the deactivated catalyst can be reactivated by short-term treatment with hydrogen. A 0.1% Ru/Al2O3 catalyst is suggested. In the surface ignition regime, this catalyst can reduce the residual CO concentration from 0.8 vol % to 10–15 ppm at O2/CO = 1 even in the presence of H2O and CO2 (up to ~20 vol %) at a volumetric flow rate of ~100 1 (g Cat)?1 h?1, which is one magnitude higher than the flow rates reported for this process in the literature.  相似文献   

20.
A series of beta-diketone ligands, R(1)COCH(2)COR(2) [tmhdH (R(1) = R(2) = C(CH(3))(3)); tfacH (R(1) = CF(3); R(2) = CH(3)); hfacH (R(1) = R(2) = CF(3))], in combination with tert-butyl peracetate (t-BuPA), have been investigated as etchant solutions for dissolution of copper metal into carbon dioxide solvent. Copper removal in CO(2) increases in the order tfacH < tmhdH < hfacH. A study of the reactions of the hfacH/t-BuPA etchant solution with metallic copper and zinc was conducted in three solvents: scCO(2) (supercrical CO(2)); hexanes; CD(2)Cl(2). The etchant solution/metallic zinc reaction produced a diamagnetic Zn(II) complex, which allowed NMR identification of the t-BuPA decomposition products as tert-butyl alcohol and acetic acid. Gravimetric analysis of the amount of zinc consumed, together with NMR studies, confirmed the 1:1:2 Zn:t-BuPA:hfacH reaction stoichiometry, showing t-BuPA to be an overall two-electron oxidant for Zn(0). The metal-containing products of the copper and zinc reactions were characterized by elemental analysis, IR spectroscopy, and, as appropriate, NMR spectroscopy and single-crystal X-ray diffraction [trans-M(hfac)(2)(H(2)O)(CH(3)CO(2)H) (1, M = Cu; 2, M = Zn)]. On the basis of the experimental results, a working model of the oxidative dissolution reaction is proposed, which delineates the key chemical variables in the etching reaction. These t-BuPA/hfacH etchant solutions may find application in a CO(2)-based chemical mechanical planarization (CMP) process.  相似文献   

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