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Titlebook: Characterization of Porous Solids and Powders: Surface Area, Pore Size and Density; S. Lowell,Joan E. Shields,Matthias Thommes Book 2004 S

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11#
發(fā)表于 2025-3-23 13:37:04 | 只看該作者
,Die Preiskompetenz des Verk?ufers,The vacuum volumetric, or static, method is used to determine the monolayer capacity of a catalyst sample from which certain important characteristics such as active metal area, dispersion, crystallite size, etc., may be derived by the acquisition of adsorption isotherms.
12#
發(fā)表于 2025-3-23 17:18:46 | 只看該作者
Preisvergleich und Preisstrukturen,Under conditions of dynamic flow, controlled heating rates can be used to acquire characteristic reaction rate curves that can be used to classify, or fingerprint, different catalysts.
13#
發(fā)表于 2025-3-23 20:20:44 | 只看該作者
14#
發(fā)表于 2025-3-24 01:15:44 | 只看該作者
Mercury Porosimetry: Non-wetting Liquid PenetrationThe method of mercury porosimetry for the determination of the porous properties of solids is dependent on several variables. One of these is the wetting or contact angle between mercury and the surface of the solid.
15#
發(fā)表于 2025-3-24 02:56:39 | 只看該作者
16#
發(fā)表于 2025-3-24 08:38:38 | 只看該作者
Volumetric Chemisorption: Catalyst Characterization by Static MethodsThe vacuum volumetric, or static, method is used to determine the monolayer capacity of a catalyst sample from which certain important characteristics such as active metal area, dispersion, crystallite size, etc., may be derived by the acquisition of adsorption isotherms.
17#
發(fā)表于 2025-3-24 12:44:18 | 只看該作者
18#
發(fā)表于 2025-3-24 17:45:56 | 只看該作者
https://doi.org/10.1007/978-1-4020-2303-3Activation energy; Adsorption Isotherms; Chemisorption; Gas Adsorption; Langmuir and BET Theories; Non-We
19#
發(fā)表于 2025-3-24 19:01:52 | 只看該作者
978-90-481-6633-6Springer Science+Business Media B.V. 2004
20#
發(fā)表于 2025-3-25 03:10:39 | 只看該作者
Surface Area Analysis from the Langmuir and BET Theoriesphysisorption isotherms of type I. Although this type of isotherm is usually observed with microporous adsorbents, due to the high adsorption potential, a separation between monolayer adsorption and pore filling is not possible for many such adsorbents.
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