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911.
Pd-supported on WO3–ZrO2 (W/Zr atomic ratio=0.2) calcined at 1073 K was found to be highly active and selective for gas-phase oxidation of ethylene to acetic acid in the presence of water at 423 K and 0.6 MPa. Contact time dependence demonstrated that acetic acid is formed via acetaldehyde formed by a Wacker-type reaction, not through ethanol by hydration of ethylene.  相似文献   
912.
A new concept for the processing and fabrication of rigid-rod molecular composites aiming at the elimination or minimization of phase separation is proposed. This approach calls for a coil-like aromatic polyisoimide which is soluble and compatible with an amorphous matrix polymer or thermosettable oligomer and can undergo facile transformation to the corresponding rigid-rod polyimide in solid composite state, thus imparting the inherently high strength/high modulus properties to the final form. To this end, various synthetic routes were explored to obtain para-diamines which could afford high molecular weight and aprotic-solvent-soluble polyisoimides upon polymerization with pyromellitic dianhydride (PMDA). Four such polyisoimides were prepared, with their inherent viscosities ranging from 0.25 to 1.89 dl g−1 in dimethylacetamide at 30°C. Facile thermally induced isoimide-imide conversion was demonstrated by solid-state (film) Fourier transform infrared spectroscopy. A preliminary evaluation of the compatibility of the polyisoimide/matrix resin was made. In one instance, a film prepared from the polyisoimide derived from PMDA and 3,3′,5,5′-tetramethylbenzidine (TMB) showed no visually detectable phase separation.  相似文献   
913.
利用微波介电加热和微波干燥水解法制备TiO2微粒   总被引:4,自引:0,他引:4  
欧阳志强  刘桂华 《江西化工》2003,(4):133-136,150
利用微波介电加热和微波干燥条件下TiCl4直接水解的方法制备出平均尺寸为40m,粒径分布窄,均为球形且形态均一,团聚较少,金红石型的TiO2纳米粒子,其内部品粒平均大小为17nm。而传统加热和干燥条件下形成的纳米微粒平均为60nm,粒经大小不均一,形态较不规则,团聚严重。微波加热和干燥方法具有清洁、快速均匀高效、环境友好的优点,推广前景良好。TiCl4水解法经济便利,适于工业化生产。  相似文献   
914.
A VPO/TiO2 catalyst tested in the oxydehydrogenation reaction (ODH) of propane between 300 and 400°C shows satisfactory performances (up to 80% of propene selectivity at 2% of propane conversion at 300°C or 56% of propene selectivity at 9% of propane conversion at 400°C). Addition of water or pyridine in the feed gas tends to decrease the propane conversion and enhances the propene selectivity. It is shown that water increases the number of Brönsted surface acid sites by dissociative adsorption which, in turn, enhances propene selectivity at the expense of the COx selectivity. These results are in good agreement with spectroscopic IR observations performed under catalytic conditions showing that the Lewis acid sites are linked to COxformation, whereas it seems that Brönsted sites would rather be linked to propene formation.  相似文献   
915.
Co-evaporation technique from three sources was used to prepare Cu(In, Ga)Se2 polycrystalline thin films for photovoltaic conversion. Their conductivity was studied in the range 20–300 K. The grain boundary scattering mechanism is mainly responsible for the diffusion process in the latter materials. In the low temperature region, we interpret the data in terms of Mott law and the analysis is very consistent with the variable range hopping. However, thermoionic emission is predominant at high temperatures. When the conductivity deviates from the classical grain boundary conduction models, inhomogeneity is then considered and parameters such as the standard deviation and the mean potential barrier height are derived. Transmittance measurements yielded band gap values of 1.07 and 1.64 eV for CuInSe2 and CuGaSe2, respectively.  相似文献   
916.
A novel technology of removing H2S with cupric chloride solution was developed in this paper. Cupric as the form of CuS deposition, the CuS produced was then oxidized by excessive cupric ion in another reactor meanwhile cupric ion that has been consumed can be recovered by the oxidization of CuCl2- with oxygen in air,and the solution can be circulated. Moreover, the leaching kinetics of CuS by cupric ion was studied. The removal efficiency of H2S is close to 100%, and the required operating condition is mild. Compared with other wet oxidization methods, no raw material is consumed except O2 in air, the process has no secondary pollution and no problem of degradation and scale, and the absorbent is much stable and reliable.  相似文献   
917.
用氧指数 (LOI) ,TG法测定研究了 2 ,4,6-三溴苯胺 (TBA)对环氧树脂酸酐固化物阻燃耐热性的影响 ,结果表明 TBA能较好地阻燃树脂固化物 ,TBA与 Sb2 O3 和磷酸三苯酯 (TPP)配用时具有阻燃协同效应 ,且对环氧树脂酸酐固化物的热稳定性影响较小。  相似文献   
918.
以新型稀土复合固体超强酸为催化剂,在微波辐射下苯甲醇和乙酸反应合成了乙酸苄酯,探索反应各因素对酯化率的影响。实验结果表明:SO4^2-/ZrO2-Nd2O3具有较高的催化活性。最佳反应条件为:醇酸摩尔比2.0(乙酸用量为0.2mol前提下),催化剂用量为1.8g,带水剂环己烷12mL,微波辐射功率550W,辐射时间25min,酯化率可达96.3%。该催化剂易于回收且可重复使用,具有良好的活性稳定性。  相似文献   
919.
Au-based catalysts, known for ambient temperature CO oxidation, have to provide stable performance of up to 5000 h in order to be commercially applicable in automotive fuel cells. In this report, the on-line deactivation characteristics of Au/TiO2 in unconventional PROX conditions are discussed. As opposed to CO removal from air, results in this report suggests that carbonates have a minor effect on deactivation of Au/TiO2 in dry H2-rich conditions. Also, no conclusive correlation between surface hydration and deactivation was observed. Rather, deactivation appeared to have occurred as a result of an intrinsic transformation in the oxidation state of the active species in the reducing operating conditions; a process which was reversible in an oxidizing atmosphere.  相似文献   
920.
绘制了阳离子表面活性剂R12TAB/正丁醇/正癸烷/水体系的拟三元相图,确定了微乳液区、微乳液/液晶共存区及不同液晶区域的范围。用^2HNMR和差示扫描量热法(DSC)与液晶纹理相互对照,研究了该体系的液晶结构特点。结果表明:含质量分数为25%~75%正癸烷的各相图内,除了存在着层状、六角状单相液晶区和层状/六角状/立方状共存的混合液晶区域外,还存在着液晶/微乳液共存的区域,且随着正癸烷质量分数的增加,微乳液及液晶区域逐渐缩小。  相似文献   
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