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111.
固体吸附式制冷系统中吸附剂一般是多孔介质结构,吸附剂的内部结构特征对传热特性和吸附质的传质特性有直接影响,进而影响吸附解吸时间。本文探讨利用分形理论来分析固体吸附剂的结构特点,为目前通过对吸附剂的固化处理来提高吸附剂的传热速率的处理方法提供理论上的分析,并指出最佳分形维数的分形结构。 相似文献
112.
113.
Adaptation of the microscopic properties of redox catalysts to the type of gas-solid reactor 总被引:1,自引:0,他引:1
Catalysts of selective oxidation usually work in a simultaneous redox mode in reactant/air cofed reactors. The solid must provide selective lattice oxygen according to a kinetic mechanism depending on operating conditions that differ from one reactor to another. Better catalytic performance can be obtained in a recirculating solids reactor because it allows separate optimization of the reduction and oxidation steps. Among the microscopic properties of the catalyst, the crystal morphology is to be taken into account because it influences its reactivity on stream. These considerations lead to a new approach of the catalyst-reaction-reactor trio. 相似文献
114.
聚合物电解质PEO全固态电致变色窗 总被引:3,自引:0,他引:3
本文用聚合物PEO的锂盐络合物作电解质制作全固态电致变色窗,讨论了器件的特性,以及工艺条件的影响。 相似文献
115.
液相对流对固液界面稳定性的影响 总被引:1,自引:0,他引:1
以模型合金丁二腈-乙醇的强制性晶体生长为基础,利用自行研制的液相对流驱动装置,详细考查了液相自然对流及强迫对流作用下,模型合金平界面失稳的动态生长过程,证实了液相的流动加快了液相温度与浓度分布的均匀化,从而增强了液/固界面的稳定性。并且随流动速度的增加,界面稳定性提高。 相似文献
116.
聚氧乙烯 - 聚氧丙烯 - 聚苯乙烯多嵌段聚合物的力学和导电性能研究 总被引:1,自引:0,他引:1
研究了聚苯乙烯含量对聚氧乙烯-聚氧丙烯-聚苯乙烯多嵌段聚合物的力学性能及其与LiClO4络合物的离子导电性能的影响;并以电导率较高的络合物为电解质,Na1+xV3O8复合物和Li片分别为正、负极组装了薄型锂电池并测定其放电性能。 相似文献
117.
Studies of the complete oxidation of methane on a Pt electrode-catalyst in the cell with a solid proton-conducting electrolyte (CH4 + O2, Pt ¦ SrCe0.92Dy0.08O3 ¦ Pt, H2O + N2) were carried out. The non-Faradaic effect of electrochemical hydrogen pumping on the rate of methane oxidation has been demonstrated. The induced change in the reaction rate at anodic polarization of a Pt electrode-catalyst was over two orders of magnitude higher than the rate of hydrogen pumping from the reaction zone through the electrolyte. 相似文献
118.
Catalytic chlorination of methane was studied over SO
4
2–
/ZrO2, Pt/SO
4
2–
/ZrO2, and Fe/Mn/SO
4
2–
/ZrO2 solid superacid catalysts. The reactions were carried out in a continuous flow reactor under atmospheric pressure, at temperatures below 240°C, with a gaseous hourly space velocity of 1000 ml/g h and a methane to chlorine ratio of 4 to 1. At 200°C with 30% chlorine converted the selectivity in methyl chloride exceeds 90%. At more elevated temperatures, the selectivity decreases but stays above 80% in methyl chloride at 225°C using the sulfated zirconia catalysts. The selectivity can be enhanced by adding platinum to sulfated zirconia catalysts. An iron and manganese-doped catalyst exhibited excellent selectivities at somewhat lower conversions. Methyl chloride is obtained at 235°C in selectivities greater than 85%. No chloroform or carbon tetrachloride is formed. The electrophilic insertion involves electron-deficient metal-coordinated chlorine into the methane C-H bond.Catalysis by solid superacids, 29. For part 28 see ref. [14]. 相似文献
119.
Savitree Jungsakulrujirek & Athapol Noomhorm 《International Journal of Food Science & Technology》1998,33(4):367-374
The effect of fruit size and harvesting of Thai tangerine fruit ( Citrus reticulata , Blanco) at different growth stages, 8–12 months after fruit set, on the distribution of limonin in whole fruit as well as in the individual fruit parts and extracted juice was investigated. The highest limonin concentration was observed in seed, followed by albedo, flavedo, segment membrane and juice sacs in decreasing order. The limonin concentration in juice as well as in whole fruit was decreased when fruit was harvested 8–12 months of fruit set. Increasing harvesting time from 8 to 12 months showed corresponding decreases in the amount of limonin in flavedo, albedo and seed. There was a decrease in titrable acidity and increase in total soluble solid and total soluble solid/titrable acidity ratio of juice with a later than normal harvesting time. However, fruit size showed no effect on limonin content and other properties of juice extracted from tangerine. 相似文献
120.
The equilibrium reaction 3'(Fe, Co)O'( ss ) +1/2O2 ( g ) ⇄ (Fe, Co)3 O4 ( ss ) was studied in the temperature range 970 to 1370 K for seven different total compositions of molar ratios 0.5 < Fe/(Fe + Co) ≤ 1.0. The equilibrium pressures of oxygen were determined by using galvanic cells incorporating calcia stabilized zirconia as solid electrolyte and the Fe/Co ratios in the solid-solution phases by wavelength dispersive spectrometry microprobe analyses. The activities of 'FeO' in the cobaltowüstite phase were then derived from the experimental results obtained. 相似文献