首页> 外文会议>5th International Symposium on the Characterisation of Porous Solids (COPS-V), Heidelberg, Germany, May 30-June 2, 1999 >Adsorption mechanism of water on carbon micropore with in situ small angle x-ray scattering
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Adsorption mechanism of water on carbon micropore with in situ small angle x-ray scattering

机译:原位小角X射线散射对水在碳微孔上的吸附机理

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The in situ small-angle X-ray scattering (SAXS) profiles of water adsorbed on pitch-based activated carbon fibers (ACF) of the pore width omega = 0.8 and 1.1 nm were measured at 303K and different relative pressures. The SAXS spectrum of ACF of omega = 1.1 nm in the direction of desorption did not overlap that in the adsorption direction, showing the hysteresis behavior. The Ornstein-Zernike (OZ) theory was applied to analyze the SAXS data in order to investigate hte structure of water molecular assembly in the carbon micropore using the density fluctuation of the system. These data lead that water molecules produce the large clusters in the micropore, and these clusters have different structures on the courses of adsorption and desorption. On the other hand, the SAXS profiles of ACF of omega = 0.8 nm at different relative pressures has no hysteresis coinciding that the water adsorption isotherm has no hysteresis. These results explicitly suggest that the structures of the water molecular assemblies on absorption and desorption are different from each other in case of the presence of adsorption hysteresis.
机译:在303K和不同的相对压力下测量了吸附在孔径为ω= 0.8和1.1 nm的沥青基活性炭纤维(ACF)上的水的原位小角X射线散射(SAXS)曲线。在解吸方向上,ω= 1.1 nm的ACF的SAXS光谱与吸附方向上的SAXS光谱不重叠,显示出滞后行为。为了通过系统的密度波动研究碳微孔中水分子组装的结构,采用了Ornstein-Zernike(OZ)理论来分析SAXS数据。这些数据导致水分子在微孔中产生大的簇,并且这些簇在吸附和解吸过程中具有不同的结构。另一方面,在不同的相对压力下,ω= 0.8 nm的ACF的SAXS曲线没有滞后现象,这说明吸水等温线没有滞后现象。这些结果明确表明,在存在吸附滞后的情况下,水分子组装体在吸收和解吸时的结构彼此不同。

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