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Adsorpcja monopodstawionych fenoli na węglach aktywnych o zróżnicowanym charakterze chemicznym powierzchni

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EN
Adsorption of monosubstituted phenols onto activated carbons with different surface characteristics
Języki publikacji
PL
Abstrakty
PL
W pracy zbadano wpływ charakteru chemicznego powierzchni węgla aktywnego na adsorpcję wybranych monopodstawionych fenoli. Wyjściowy węgiel aktywny CWZ 22 poddano demineralizacji, działaniu nadtlenku wodoru, amoniaku i wygrzewaniu w wysokiej temperaturze w atmosferze inertnej. Otrzymane węgle różniły się zawartością kwasowych i zasadowych grup funkcyjnych i wartością pHPZC. Procesy modyfikacji nie wpłynęły zasadniczo na strukturę porowatą węgli aktywnych. Adsorpcję 2-chlorofenolu (OCF), 4-chlorofenolu (PCF) i 4-nitrofenolu (PNF) przeprowadzono w warunkach statycznych. Czasy osiągania stanu równowagi rosły w kierunku OCF < PCF < PNF. Wyznaczone nadmiarowe izotermy adsorpcji interpretowano, opierając się na modelu Freundlicha i Langmuira. Wykazano, że do stężenia równowagowego około 125 mg/dm³ równanie Langmuira lepiej opisuje adsorpcję fenoli niż równanie Freundlicha. Węgiel aktywny po wygrzewaniu w temperaturze 800°C w atmosferze azotu charakteryzował się największą pojemnością sorpcyjną względem badanych monopodstawionych fenoli. Obróbka termiczna w podanych warunkach spowodowała wyraźny wzrost wartości pHPZC i zmniejszenie zawartości powierzchniowych tlenowych grup kwasowych.
EN
The effect of the carbon surface chemistry on the adsorption of 2-chlorophenol (OCF), 4-chlorophenol (OCP) and 4-nitrophenol (PNP) has been studied. To obtain a series of activated carbons with different content of acidic and basic functionalities and pHPZC value, the initial activated carbon CWZ 22 was subjected to the demineralization with inorganic acids (CWZ dem), the treatment with 20% hydrogen peroxide (CWZ H2O2), the treatment with ammonia at 450°C (CWZ NH3), and heat treatment in an inert atmosphere at 800°C (CWZ N2). For the obtained carbons, pHPZC ranged from 5.85 to 10.08 and increased in the following direction: CWZ H2O2 < CWZ dem < CWZ 22 < CWZ NH3 < CWZ N2. The applied treatments changed insignificantly the porous structure of the activated carbon. The adsorption process of selected monosubstituted phenols was carried out in static conditions, maintaining solution pH below pKa of a given adsorbate. The equilibrium time of adsorption process of phenols increased in the direction: OCF < PCF < PNF. For CWZ NH3 and CWZ N2 carbons the equilibrium time was the shortest whereas the longest time was required in the case of CWZ H2O2. The adsorption of phenols on the tested activated carbons proceeded relatively fast. Around 50% of the maximum sorption capacity was attained after 1 h of the process. The Langmuir and Freundlich models were applied to interpret the adsorption isotherm data. It was found that up to around 125 mg/dm³ of the equilibrium concentration, the Langmuir model better describes the adsorption system than the Freundlich equation. In this range of concentrations the extent of adsorption decreased with increasing the adsorbate solubility. For studied activated carbons, except for CWZ H2O2, the calculated surface monolayer coverage by adsorbate molecules is higher than 0.7. The obtained results suggest that the multilayer adsorption was probably responsible for a rapid increase in the adsorbed amount that was observed at higher equilibrium concentrations. The activated carbon heated under nitrogen flow at high temperature showed the highest adsorption capacity toward monosubstituted phenols. Heat treatment of initial activated carbon led to a marked increase in the pHPZC value and a decrease in the acidic groups content. The oxidation of CWZ 22 resulted in a increase in the oxygen surface functionalities and as a result, CWZ H2O2 was characterized by the lowest efficiency in the removal of phenols from aqueous solution.
Rocznik
Strony
173--184
Opis fizyczny
Bibliogr. 21 poz.
Twórcy
  • Politechnika Wrocławska, Wydział Chemiczny, Zakład Materiałów Polimerowych i Węglowych, ul. Gdańska 7/9, 50-344 Wrocław
Bibliografia
  • [1] Daifullah A.A.M., Girgis B.S., Removal of some substituted phenols by activated carbon obtained from agricultural waste, Water Res. 1998, 32,1169-1177.
  • [2] Environmental Protection Agency, Methods 604, Phenols in Federal Register, October 26, Part VIII, 40 cfr, Part 136, 5879, 1984.
  • [3] Jain A.K., Bhatnagar S., Bhatnagar A., Methylphenols removal from water by low-cost adsorbents, J. Colloid Interface Sci. 2002, 251, 39-45.
  • [4] Hsieh C.T., Teng H., Liquid-phase adsorption of phenol onto activated carbons prepared with different activation levels, J. Colloid Interface Sci. 2000, 230, 171-175.
  • [5] Streat M., Partick J. W., Camporro Perez M.J., Sorption of phenol and para-chlorophenol from water using conventional and novel activated carbons, Water Res. 1995, 29, 467-472.
  • [6] Radovic L.R., Moreno-Castilla C, Rivera-Utrilla J., Carbon materials as adsorbents in aqueous solution, (w:) (ed. Radovic L.R.) Chemistry and Physics of Carbon, Volume 27, Marcel Decker, New York, Basel 2001.
  • [7] Dębowski Z., Kryteria doboru węgla aktywnego, Prace Naukowe, Główny Instytut Górnictwa, Katowice 1994.
  • [8] Julien F., Baudu M., Mazet M., Relationship between chemical and physical surface properties of activated carbon, Water Res. 1998, 32, 3414-3424.
  • [9] Radovic L.R., Silva I.F., Ume J.I., Menendez J.A., Leon Y Leon C.A., Scaroni A.W., An experimental and theoretical study of the adsorption of aromatics possessing electron-withdrawing and electron-donating functional groups by chemically modified activated carbons, Carbon 1997, 35, 1339-1348.
  • [10] Ania CO., Parra J.B., Pis J.J., Influence of oxygen-containing functional groups on active carbon adsorption of selected organic compounds, Fuel Process. Technol. 2002, 79, 265-271.
  • [11] Yenisoy-Karakas S., Aygun A., Gunes M., Tahtasakal E., Physical and chemical characteristics of polymer-based spherical activated carbon and its ability to adsorb organics, Carbon 2004,42,477-484.
  • [12] Vinke P., van der Eijk M., Verbree M., Voskamp A.F., van Bekkum H., Modification of the surfaces of a gas-activated carbon and a chemically activated carbon with nitric acid, hypochlorite and ammonia, Carbon 1994, 32, 675-686.
  • [13] Moreno-Castilla C, Lopez-Ramon M.V., Carrasco-Marin F., Changes in surface chemistry of activated carbons by wet oxidation, Carbon 2000, 38, 1995-2001.
  • [14] Daifullah A.A.M., Girgis B.S., Removal of some substituted phenols by activated carbon obtained from agricultural waste, Water Res. 1998, 32, 1169-1177.
  • [15] Mattson J.S., Mark Jr. H.B., Malbin M.D., Weber Jr. W.J., Crittenden J.C., Surface chemistry of active carbon: specific adsorption of phenols, J. Colloid Interface Sci. 1969, 31,116-130.
  • [16] Nevskaia D.M., Santianes A., Munoz V., Guerrero-Ruiz A., Interaction of aqueous solutions of phenol with commercial activated carbons: an adsorption and kinetic study, Carbon 1999, 37,1065-1074.
  • [17] Franz M., Arafat A.H., Pinto N.G., Effect of chemical surface heterogeneity on me adsorption mechanism of dissolved aromatics on activated carbon, Carbon 2000, 38, 1807-1819.
  • [18] Muller E., Gubbins K., Molecular simulation study of hydrophilic and hydrophobic behavior of activated carbon surface, Carbon 1998, 36, 1433-1438.
  • [19] Haghseresht F., Lu G.Q., Whittaker A.K., Carbon structure and porosity of carbonaceous adsorbents in relation to their adsorption properties, Carbon 1999, 37, 1491-1497.
  • [20] Nevskaia D.M., Castillejos-Lopez E., Guerrero-Ruiz A., Munoz V., Effects of the surface chemistry of carbon materials on the adsorption of phenol-aniline mixtures from water, Carbon 2004, 42, 653-665.
  • [21] Trochimczuk A.W., Aoki S., Yamabe K., Jyo A., Synthesis of porous divinylbiphenyl copolymers and their sorptive properties towards phenol and its derivatives, Eur. Polym. J. 2002, 38, 1175-1181.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-LOD3-0005-0003
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