1999
DOI: 10.1016/s0008-6223(98)00182-1
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Vapor adsorption on coal- and wood-based chemically activated carbons

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Cited by 36 publications
(12 citation statements)
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“…However, for the adsorbent samples prepared by H 2 SO 4 activation, the data obtained are dispersed, suggesting that the adsorptive capacity is not solely a function of the BET surface area. A similar observation was also reported by Lee and Reucroft when they studied the adsorption of NH 3 onto wood-base activated carbons prepared by phosphoric acid (H 3 PO 4 ) in the very low relative pressure range [14]. Besides the tests carried out at 323 K, NH 3 adsorption tests for a wide range of temperatures from 303 to 373 K were also carried out for the activated carbons prepared at 973 K for 2 h by thermal activation and chemical activation (20% H 2 SO 4 impregnation).…”
Section: Resultssupporting
confidence: 85%
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“…However, for the adsorbent samples prepared by H 2 SO 4 activation, the data obtained are dispersed, suggesting that the adsorptive capacity is not solely a function of the BET surface area. A similar observation was also reported by Lee and Reucroft when they studied the adsorption of NH 3 onto wood-base activated carbons prepared by phosphoric acid (H 3 PO 4 ) in the very low relative pressure range [14]. Besides the tests carried out at 323 K, NH 3 adsorption tests for a wide range of temperatures from 303 to 373 K were also carried out for the activated carbons prepared at 973 K for 2 h by thermal activation and chemical activation (20% H 2 SO 4 impregnation).…”
Section: Resultssupporting
confidence: 85%
“…Their hydrogen bonding (N-H· · ·O) energy has been reported to be as much as 3 kcal/mol [14]. NH 3 can therefore preferably adsorb onto active adsorption sites provided by oxygen functional groups via hydrogen boding besides on pure carbon sites.…”
Section: Resultsmentioning
confidence: 99%
“…However, several works report a decrease in phenol adsorption from water with surface oxidation Mahajan et al, 1980;Leng, 1996;Franz et al, 2000;Terzyk, 2003Terzyk, , 2004Moreno-Castilla, 2004). Since lignites are rich in oxygen surface groups Küçükbayrak et al, 2000), they have a high affinity for water (Allardice and Evans, 1971;Schafer, 1972;Kaji et al, 1986;Müller and Gubbins, 1998;Lee and Reucroft, 1999). Therefore, the decrease in adsorption with oxidation is attributed to the preferential hydration of the surface oxygen groups over the hydrogen-bonding of the -OH of the phenol molecule.…”
Section: Discussionmentioning
confidence: 99%
“…Those adsorbents include untreated zeolites, carbonaceous materials, and alumina [1,[8][9][10][11][12][13][14][15][16][17][18][19][20]. Ammonia adsorption was studied either from the air filtration standpoint or as a way to characterize the acid-base nature of an adsorbent.…”
Section: Introductionmentioning
confidence: 99%