1995
DOI: 10.1021/ef00050a018
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Pore Structure of the Argonne Premium Coals

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Cited by 92 publications
(120 citation statements)
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(4 reference statements)
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“…The same conclusion can be inferred from the work of Larsen et al 24 Another significant characteristic that can be drawn from the results of the TW series is that the adsorption of CO 2 tends to decrease with the increase in the density of separation, i.e. more microporous material is found at lower relative densities.…”
Section: Adsorption Isotherms In Cosupporting
confidence: 79%
“…The same conclusion can be inferred from the work of Larsen et al 24 Another significant characteristic that can be drawn from the results of the TW series is that the adsorption of CO 2 tends to decrease with the increase in the density of separation, i.e. more microporous material is found at lower relative densities.…”
Section: Adsorption Isotherms In Cosupporting
confidence: 79%
“…The specific surface areas of NOM based on CO 2 adsorption differ significantly from those using N 2 adsorption, primarily due to the molecular sieving phenomenon (De Jonge and Mittelmeijer-Hazeleger, 1996;Xing and Pignatello, 1997). Some internal pores of organic matrices can not be approached by N 2 (Gan et al, 1972;Larsen et al, 1995). Carbon dioxide at 273 K and benzene at 295 K have been used as alternative gases for probing the surface properties of carbonaceous materials (Corley et al, 1996;De Jonge and Mittelmeijer-Hazeleger, 1996;Kwon and Pignatello, 2005;Ravikovitch et al, 2005;Xing and Pignatello, 1997).…”
Section: Introductionmentioning
confidence: 99%
“…where n ex is the experimentally measured amount of adsorption, q is the density of the gas phase, q a is the density of the adsorbed phase, n o is the adsorption/micropore capacity, b is the affinity coefficient between CO 2 and the coal (b = 0.35 for CO 2 ) [40], E o is the characteristic heat of adsorption, j is the structural heterogeneity parameter, P s is the saturation pressure, R is the universal gas constant, T is the temperature, and DV is the unaccounted-for volume due to the gas solubility in the coal matrix, to the coal swelling, and to any over-or under-estimation of the void volume (V o ) in the sample cell due to the assumptions underlying the choice of helium as the reference gas in the adsorption experiments [41][42][43][44][45][46]. The saturation pressure (P s ) and the density of the adsorbed phase (q a ) were calculated using the relationships suggested by Reid et al [47] and Dubinin [48], respectively.…”
Section: Evaluation Of the Adsorption Isotherm Datamentioning
confidence: 99%