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The influence of pre-adsorbed water on adsorption of methane on fumed and nanoporous silicas

机译:预吸附水对气相二氧化硅和纳米多孔二氧化硅吸附甲烷的影响

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摘要

Co-adsorption of water and methane onto fumed (A-300, A-380) and micro/mesoporous (Gasil 200DF) silicas was studied. FTIR and ~1H NMR spectroscopy with layer-by-layer freezing-out of bound water were used at different levels of hydration (h = 0.005-1.0 g of water per gram of silica). Methane adsorption was largest (l-2wt% at T<280k) for nanosilica A-300 (S_(BET) = 337m~2/g) at hydration h = 0.1g of water per gram of silica for a non-equilibrated system. This sample was characterised by a large amount of weakly associated water (δh≈1 ppm), and maximal clustering of all bound water. These conditions provide the increased microporosity necessary for enhanced methane adsorption. Heating and subsequent wetting, or long equilibration of nanosilica, decreased the adsorption of methane. The adsorption of methane on silica 200DF decreased with increasing amounts of pre-adsorbed water, characterised by significant associativity (δH≈ 5 ppm) at h ≥ 0.005 g/g.
机译:研究了水和甲烷在气相(A-300,A-380)和微/中孔(Gasil 200DF)二氧化硅上的共吸附。 FTIR和〜1H NMR光谱具有逐层冻结结合水的作用,用于不同的水合水平(h =每克二氧化硅0.005-1.0 g水)。对于非平衡体系,在水合作用h = 0.1g水/克二氧化硅时,纳米二氧化硅A-300的甲烷吸附最大(在T <280k时为1-2wt%)(S_(BET)= 337m2 / 2 / g)。该样品的特征是大量的弱缔合水(δh≈1ppm)和所有结合水的最大聚集。这些条件提供了增强的甲烷吸附所需的增加的微孔率。加热和随后的润湿或纳米二氧化硅的长时间平衡降低了甲烷的吸附。甲烷在二氧化硅200DF上的吸附随着预吸附水量的增加而降低,其特征是在h≥0.005 g / g时具有显着的缔合性(δH≈5ppm)。

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