Adsorption kinetics and thermodynamics of azo-dye Orange II onto highly porous titania aerogel

被引:282
作者
Abramian, Lara [1 ]
El-Rassy, Houssam [1 ]
机构
[1] Amer Univ Beirut, Dept Chem, Beirut 11072020, Lebanon
关键词
Adsorption isotherm; Adsorption kinetics; Titania aerogel; Azo-dye; Orange II; AQUEOUS-SOLUTIONS; ACTIVATED CARBON; SILICA AEROGELS; WASTE MATERIALS; ACID ORANGE-7; BOTTOM ASH; REMOVAL; ADSORBENT; SURFACE; WATER;
D O I
10.1016/j.cej.2009.01.019
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We report herein a kinetic and thermodynamic study of the adsorption of azo-dye Orange II from aqueous solutions onto titania aerogels. Aerogels structure was confirmed by MR and N-2 adsorption revealed their specific surface area (500 m(2)/g), pore volume (2.86 cm(3)/g) and pore size (mean 13.9 nm). Adsorption tests were conducted in batch reactors under various conditions where the effect of pH, temperature. contact time, dye concentration, and adsorbent dose were studied. Experiments performed at pH 2 show the optimal adsorption due to the best surface charge interactions. The temperature shows a weak influence with a decrease in the adsorption uptake as the temperature increases. Adsorption kinetics is shown to be very fast and follows a pseudo second-order indicating the coexistence of chemisorption and physisorption with the intra-particle diffusion being the rate controlling step. The experimental data fit perfectly with Sips isotherms and reveal the ability of titania aerogel to adsorb 420 mg of Orange II per gram of adsorbent at the optimal conditions. The thermodynamic study reveals the activation energy (42.1 kJ mol(-1)) and the changes in Gibbs free energy (1.2 kJ mol(-1)), enthalpy (-16.4 kJ mol(-1)), and entropy(-58 J mol(-1) K-1). The entire regeneration of the titania aerogel adsorption sites at pH 11 and 30 degrees C shows a total recovery of the dye and the efficient reusability and the economic interest of these adsorbing materials for environmental purposes. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 410
页数:8
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