Measurement and interpretation of unary supercritical gas adsorption isotherms in micro-mesoporous solids
Autor: | Ronny Pini, Humera Ansari, Junyoung Hwang |
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Rok vydání: | 2021 |
Předmět: |
Technology
Engineering Chemical Materials science Excess and net adsorption General Chemical Engineering 0904 Chemical Engineering Thermodynamics 02 engineering and technology 010402 general chemistry 01 natural sciences High-pressure gas storage Textural characterisation Engineering Adsorption Physisorption Phase (matter) 0912 Materials Engineering Zeolite Science & Technology Chemical Physics Chemistry Physical Surfaces and Interfaces General Chemistry Microporous material 021001 nanoscience & nanotechnology Supercritical fluid 0104 chemical sciences Chemistry Physical Sciences Supercritical adsorption 0210 nano-technology Mesoporous material |
Zdroj: | Adsorption. 27:659-671 |
ISSN: | 1572-8757 0929-5607 |
DOI: | 10.1007/s10450-021-00313-z |
Popis: | Gas adsorption at high pressures in porous solids is commonly quantified in terms of the excess amount adsorbed. Despite the wide spectrum of adsorbent morphologies available, the analysis of excess adsorption isotherms has mostly focused on microporous materials and the role of mesoporosity remains largely unexplored. Here, we present supercritical CO2 adsorption isotherms measured at $$T=308$$ T = 308 K in the pressure range $$p=0.02{-}21$$ p = 0.02 - 21 MPa on three adsorbents with distinct fractions of microporosity, $$\phi_2$$ ϕ 2 , namely a microporous metal-organic framework ($$\phi_2=70$$ ϕ 2 = 70 %), a micro-mesoporous zeolite ($$\phi_2=38$$ ϕ 2 = 38 %) and a mesoporous carbon ($$\phi_2 ϕ 2 < 0.1 %). The results are compared systematically in terms of excess and net adsorption relative to two distinct reference states–the space filled with gas in the presence/absence of adsorbent–that are defined from two separate experiments using helium as the probing gas. We discuss the inherent difficulties in extracting from the supercritical adsorption isotherms quantitative information on the properties of the adsorbed phase (its density or volume), because of the nonuniform distribution of the latter within and across the different classes of pore sizes. Yet, the data clearly reveal pore-size dependent adsorption behaviour, which can be used to identify characteristic types of isotherm and to complement the information obtained using the more traditional textural analysis by physisorption. |
Databáze: | OpenAIRE |
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