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91.
92.
SAPO-34/SiO_2催化甲醇制烯烃 总被引:2,自引:0,他引:2
采用水热法合成了SAPO-34分子筛,并用X射线粉末衍射仪和扫描电子显微镜对SAPO-34分子筛的结构进行了表征,同时探讨了黏合剂种类、甲醇分压、催化剂粒径和硅源等对SAPO-34分子筛催化甲醇制烯烃(MTO)反应性能的影响。实验结果表明,在MTO反应中,三烯(乙烯、丙烯和丁烯)选择性在反应初期存在明显的诱导期;以S iO2为黏合剂合成的SAPO-34/S iO2催化剂不但可缩短MTO反应的诱导期,三烯选择性也较未添加黏合剂或以A l2O3为黏合剂时高1~2个百分点;且当催化剂活性明显下降时,三烯选择性下降的幅度较小。催化剂粒径、甲醇分压及硅源对催化剂的诱导期也有明显的作用。在甲醇分压低于19kPa、催化剂粒径0.25~0.38mm、S iO2为黏合剂、硅酸四乙酯为硅源时,SAPO-34/S iO2催化剂的MTO性能明显提高。 相似文献
93.
F.A Harraz 《Electrochimica acta》2002,47(8):1249-1257
The effect of chloride ions (Cl−) during the immersion plating of copper onto porous silicon (PS) from a methanol (MeOH) solution has been studied. The presence of Cl− in the Cu2+ solution was found to slow down the rate of copper deposition, as confirmed by inductively coupled argon plasma emission spectroscopy and X-ray photoelectron spectroscopy measurements. The threshold concentration of Cl− at which the deposition of copper is very severely diminished was found to be 0.1 M. The inhibition effect is discussed on the basis of the rest potential values of PS and polarization curve measurements. They revealed that the rest potential of PS upon dipping in these solutions appears to direct the metal deposition. Current density-potential curves show that at Cl− concentrations higher than 0.1 M, the reduction of Cu ions proceeds in two steps; the reduction of Cu(II) to Cu(I) followed by the reduction of Cu(I) to Cu(0). This suggests that Cu(I) species in MeOH solution can be stable over a certain potential range and this stability of Cu(I) is responsible for the inhibition of metal deposition. Fourier transform infrared spectroscopy and scanning electron microscopy (SEM) were also performed to investigate the structural changes and characterizations of PS samples after the plating process. 相似文献
94.
The surface-crack-in-flexure (SCF) method uses a Knoop indenter to create small, semielliptical surface precracks in beam specimens. Lateral cracks may interfere with the primary median crack and cause errors of up to 10% in determination of fracture toughness, particularly for materials for which the fracture toughness is ∼3 MPa·m1/2 or less. Although the residual-stress-damage zone is ground or polished away by hand by removing 4.5–5 times the indentation depth, this amount may not be sufficient to completely remove the lateral cracks in low-fracture-toughness materials. A series of tests were conducted on sintered alpha silicon carbide with different amounts of material removed after indentation. Once the lateral cracks were fully removed, the SCF results concurred with single-edged-precracked-beam and chevron-notched-beam data collected in accordance with ASTM Designation C1421. A simple remedy for the SCF method is to examine the outer ground surface for remnants of lateral cracks before fracture and to remove more material if necessary. 相似文献
95.
96.
Mechanical activation before carbothermic reduction can substantially enhance the formation of SiC from SiO2 and carbon mixtures. However, the morphology (e.g., particles or whiskers) of SiC formed from mechanically activated SiO2 and carbon mixtures is dependent of the degree of mechanical activation and the condition of the subsequent carbothermic reduction. These phenomena are investigated and rationalized based on the increased reactivity of the reactants and SiC formation mechanisms. 相似文献
97.
98.
This work employs porous silicon as a gas diffusion layer (GDL) in a micro-fuel cell. Pt catalyst is deposited on the surface of, and inside, the porous silicon by the physical vapor deposition (PVD) method, to improve the porous silicon conductivity. Porous silicon with Pt catalyst replaces traditional GDL, and the Pt metal that remains on the rib is used to form a micro-thermal sensor in a single lithographic process. 相似文献
99.
100.
草酸二甲酯加氢合成乙二醇反应的研究 总被引:7,自引:2,他引:5
在微型管式反应器中,采用Cu/SiO2催化剂,在温度190~210℃、压力1~3MPa、草酸二甲酯(DMO)与氢气的摩尔比(氢酯比)40~120、DMO空速6.0~25.0mmol/(g.h)的条件下,对DMO加氢制乙二醇的反应进行了研究。实验结果表明,高温、高压、高氢酯比和低DMO空速都能提高DMO的转化率和乙二醇的收率,但同时也增加了副产物的选择性。较适合的反应条件为:压力2MPa,温度205~210℃,氢酯比80~100,DMO空速10.0mmol/(g.h)。动力学研究表明,DMO加氢反应符合Langmuir-Hinshelwood吸附反应动力学模型,表面反应为速率控制步骤,氢气不解离吸附,由此得到了相应的动力学方程及参数。统计检验结果表明,该模型对DMO加氢反应高度适定。 相似文献