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61.
62.
Phenol adsorption on porous and non-porous carbons 总被引:1,自引:0,他引:1
Phenol physisorption on a series of porous and non-porous amorphous carbons was studied at 298 K. Grand Canonical Monte Carlo computer simulations were performed to simulate phenol adsorption from the gas phase. Phenol is adsorbed in a solid-like state within the pores and there is no well-developed multilayer regime. The ‘t’ plot method was adapted to phenol adsorption and the results obtained are in agreement with the model solids employed. The simulated adsorption isotherms were compared with experimental results obtained for adsorption from aqueous solutions of phenol. BET surface areas were calculated. Other characteristics of the adsorption system analyzed were: adsorption energy distribution functions, density profiles, distribution of molecules according to gas-solid energy, and local isotherms. 相似文献
63.
The onset of thermal convection in a translucent porous layer is considered. Attention is focused on the effect of radiative heat transfer on the critical Rayleigh-Darcy number and the convection cell shape. If we consider the contribution of radiative heat transfer, the basic temperature profile is non-linear and the thermal convective instability is influenced by the ratio of conduction to radiation heat flux, the temperatures at the boundary surfaces, and radiative parameters such as wall emissivity, scattering albedo and extinction coefficient as well as the usual Rayleigh-Darcy number. Effects of these parameters on the onset of convective instability are investigated with the help of linear stability theory employing the Darcy's law and the radiative transport equation simplified by the P1 approximation. The increased effective thermal conductivity due lo the radiation inhibits the onset of convection and causes increased critical Rayleigh-Darcy number and decreased convection cell size. The results of the present work may be exploited to find out the optimal diameter of aerogel pellets and the air pressure in the double pane window filled with the translucent silica aerogel granules to suppress natural convection. 相似文献
64.
累托石合成孔梯度多孔陶瓷的研究 总被引:2,自引:0,他引:2
以累托石为主要原料,煤粉为成孔剂,采用压制成形,在1220℃温度下烧成,制得具有一定孔梯度的多孔陶瓷,研究表明,不同的骨粒粒径及不同的成孔剂粒径的相互混合可制得具有成连续变化孔梯度分布的多孔陶瓷,且随着成孔剂含量的提高,显气孔率增加,强度和体积密度均降低。 相似文献
65.
对基于多孔介质模型开发的核电蒸汽发生器三维热工水力分析程序ATHOS进行介绍.并应用ATHOS对核电蒸汽发生器二次侧的复杂传热传质现象进行数值模拟。获得蒸汽发生器二次侧的流动换热状态,以及二次侧三维两相流场分布,分析结果可作为传热管流致振动、磨损分析及结构设计的输入数据。研究工作表明,多孔介质模型在核电蒸汽发生器设计中具有重要的应用价值。 相似文献
66.
One of the important ways to improve photocatalytic efficiency is to prepare catalyst with enhanced surface area. In this
work, titanium dioxide (TiO2) nanoparticles having enhanced surface area were synthesized under the interference of SiO2. The mixed oxide, SiO2-TiO2 (10% mol% Si), was prepared by a sol-gel procedure using titanium tetra-n-butoxide as Ti-precursor. The commercial SiO2 nanoparticles were added into the TiO2 sols after hydrolysis. After condensation and calcination heat treatment, the SiO2-TiO2 nanoparticles were obtained. To achieve the purpose of obtaining the high-surface-area TiO2, the SiO2 was removed subsequently by aqueous NaOH solution. The TiO2 products were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), electron spectroscopy for
chemical analysis (ESCA), and by N2 adsorption-desorption isotherm. A fine mesoporous structure was formed for as-prepared TiO2 after calcination at 400∘C and the average pore diameter was about 7 nm. The porous TiO2 products possess mixing phases of anatase and rutile. Phase transformation from anatase to rutile occurred when the samples
were calcined. The phase transition temperature is sensitive to the silicon content. The particle size of ∼43 nm remained
constant upon calcinations from 500 to 700∘C. The specific surface area was increased up to 66% compared to regular TiO2 samples that were prepared by the similar sol-gel procedure. The porous TiO2 nanostructures exhibited enhanced photocatalytic performance to decompose methylene blue under UV irradiation. 相似文献
67.
A. Serrano Aroca A.J. Campillo Fernndez J.L. Gmez Ribelles M. Monlen Pradas G. Gallego Ferrer P. Pissis 《Polymer》2004,45(26):8949-8955
Dynamic-mechanical and water sorption properties of porous and non-porous hydrogels have been studied as a function of their porosity and crosslinking density. Porous hydrogels with different crosslinking densities were prepared by co-polymerisation of 2-hydroxyethyl acrylate and ethyleneglycol dimethacrylate in solution in methanol. Pores were formed due to the segregation of the solvent from the polymer network during the polymerisation process. The porosity of the samples was observed by scanning electron microscopy. The pores collapse during the drying process after polymerisation but they reopen when the xerogel is immersed in liquid water. Bulk polymer networks with varying crosslinking densities were also synthesised and used as a reference in the analysis of the porous hydrogels. Water sorption from the gas phase and from the liquid phase was studied by means of equilibrium sorption isotherms and immersion experiments, respectively. Dynamic-mechanical spectroscopy conducted on the xerogels shows that the elastic modulus in the rubber-like state highly depends on the amount of solvent used in the polymerisation what is attributed to the presence of discontinuity surfaces in the xerogel although the pores are closed. 相似文献
68.
A novel high strength graphitic foam was produced through the incorporation of carbon nanofibers into a pitch based precursor. The nanofiber reinforced cellular foams were mechanically tested both from a localized and bulk perspective with results indicating enhanced foam performance with nanofiber addition. The magnitude of increased performance was a result of both the nanofiber itself as well as its heat treatment as an increase in each was found to cause an associated increase in foam performance. The increase in mechanical capability is attributed to the formation of a zigzag structure in the ligaments and nodes of the foam. This zigzag structure serves as an interlocking mechanism, preventing easy shearing of the graphene layers. The in situ fracture mechanics experiment shows brittle behavior of a single ligament indicating that only reinforced foam behaves like that of a carbon fiber. 相似文献
69.
A model is developed to address the uniformity of displacement deposition of nickel inside porous silicon with an ultrahigh aspect ratio as high as 200. The nickel distribution is treated as a current distribution issue as in electrodeposition. It is shown that the deposition distribution along the pore depth exhibits a strong dependence on a polarization parameter ξ. High values of ξ correspond to mass transport limitations and lead to non-uniform distributions, whereas small ξ values, representing interfacial reaction control, produce uniform distributions. Non-uniform deposition primarily occurs at an initial stage in which the reaction is dominated by mass transfer. As the deposition process continues, the deposition rate drops to a low value, and the deposition uniformity shifts from Ni2+ mass transport limitations to its interfacial reaction control, leading to uniform Ni2+ concentration and deposition rate distributions. It is predicted that the non-uniformity at the initial stage could be remedied by increasing the bulk concentration of the nickel ions and decreasing the plating bath pH. In addition, the uniformity of the deposition distribution can be significantly improved by introducing inhibiting additive coumarin to the plating solution. 相似文献
70.
As previously reported, high surface area microporous carbons with long-range order can be synthesized by using zeolite Y as a template. In this work, an attempt is made to synthesize porous carbon using several other types of zeolites (zeolite β, ZSM-5, mordenite and zeolite L). Special attention is paid to whether the structural regularity of each zeolite can be transferred to the carbon structure as well as with the case of zeolite Y. The carbon filling method was then examined to see which gives the highest regularity to the carbon structure. It has been found that the optimum carbon filling method for zeolite Y is not an optimum one for the other zeolites and the degree of the regularity of long-range ordering in the carbons strongly depends on zeolite type. The order of the regularity in the resultant carbons is zeolite β>>zeolite L>mordenite>ZSM-5. The effect of zeolite type on the regularity is discussed in relation to the size and the shape of the zeolite channels. 相似文献