2019
DOI: 10.1039/c8cp07751g
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Modeling of type IV and V sigmoidal adsorption isotherms

Abstract: Interpretation of type IV adsorption isotherms not by a composed but unified concept.

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Cited by 150 publications
(87 citation statements)
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References 76 publications
(123 reference statements)
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“…6). This relationship is consistent with the type V isotherm model, which indicates the presence of capillary condensation 51 . This is commonly found in porous media, where a vapour condenses at a pressure below its saturated vapour pressure [52][53][54] .…”
Section: Resultssupporting
confidence: 89%
“…6). This relationship is consistent with the type V isotherm model, which indicates the presence of capillary condensation 51 . This is commonly found in porous media, where a vapour condenses at a pressure below its saturated vapour pressure [52][53][54] .…”
Section: Resultssupporting
confidence: 89%
“…Therefore, the adsorption of VOCs slowly increases and tends to become constant. The Dubinin-Radushkevich (D-R) equation ( 30 ) was adopted to fit the corresponding isotherms; as shown, the two isotherms fit the D-R equation well (fit parameters are given in table S2).…”
Section: Resultsmentioning
confidence: 99%
“…Therefore, the adsorption of VOCs slowly increases and tends to become constant. The Dubinin-Radushkevich (D-R) equation (30) was adopted to fit the corresponding isotherms; as shown, the We measured t dynamic adsorption breakthrough curves of the HNM loaded with toluene and acetone at 200 ppmv, using the experimental apparatus shown in Fig. 6A.…”
Section: Voc Adsorption Performance Of Hnmmentioning
confidence: 99%
“…The type I water adsorption isotherm is characteristic of a hydrophilic material [ 14 , 45 ]. On the other hand, the type IV isotherm showing a sigmoidal course of an adsorption isotherm is usually observed the adsorption of water on hydrophobic porous materials such as aluminum phosphate, zeolite, metal–organic frameworks, and activated carbon [ 46 ]. Therefore, it could be speculated that the active sites of Zr(OH) 4 /GO nanocomposite are more available than those of Zr(OH) 4 , and, as a result, the soman (GD) interacts with more active sites, such that the soman (GD) hydrolysis ability of Zr(OH) 4 could be enhanced even under atmosphere water present at 80% RH.…”
Section: Resultsmentioning
confidence: 99%