1992
DOI: 10.1021/je00006a010
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Adsorption equilibrium data for substituted phenols on activated carbon

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Cited by 27 publications
(18 citation statements)
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“…For this reason, their undesirable appearance in different fluid streams is highly probable, being their separation/removal a necessary step of technical, environmental or economical concerns. There is a variety of works about aqueous-phase adsorption of PA, BA, and SA, onto adsorbent materials, as activated carbons, carbon cloths, and polymeric resins, among others (Oda et al 1981;Shirgaonkar et al 1992;Mazet et al 1994;Brasquet et al 1997;Koh and Nakajima 2000;Franz et al 2000;Ania et al 2002aAnia et al , 2002bTerzyk et al 2003;Otero et al 2005;Ayranci et al 2005;Ayranci and Duman 2006;Khenniche and Aissani 2009). …”
Section: Introductionmentioning
confidence: 99%
“…For this reason, their undesirable appearance in different fluid streams is highly probable, being their separation/removal a necessary step of technical, environmental or economical concerns. There is a variety of works about aqueous-phase adsorption of PA, BA, and SA, onto adsorbent materials, as activated carbons, carbon cloths, and polymeric resins, among others (Oda et al 1981;Shirgaonkar et al 1992;Mazet et al 1994;Brasquet et al 1997;Koh and Nakajima 2000;Franz et al 2000;Ania et al 2002aAnia et al , 2002bTerzyk et al 2003;Otero et al 2005;Ayranci et al 2005;Ayranci and Duman 2006;Khenniche and Aissani 2009). …”
Section: Introductionmentioning
confidence: 99%
“…For adsorbate and solvent the adsorption phenomenon depends on the differences between their chemical properties, structure and interactions (mutual and with solid surface). The adsorption of various series of different organic adsorbates was analyzed to find some correlations between the sorption experimental data and the properties of adsorbate and adsorbent [4,[10][11][12][13][14][15][16][17][18][19]. Many of benzene derivatives possess acidic or basic functional groups.…”
Section: Introductionmentioning
confidence: 99%
“…Equilibrium data fitted well into Langmuir equation expressed as : A glance at QO values show that adsorption capacity of phenols follow the trend P < DC < PMP < PNP < DCP. Monolayer capacity seems to increase with increasing molecuJar weight and decreasing solubility of the adsorbate in the solvent (7,8). The low adsorptive capacity for phenol may also be due to the formation of a strong hydrogen bond between the -OH group and water.…”
Section: Results and Discussion Single Solute Adsorption Systemmentioning
confidence: 99%