Adsorptive Removal of Sulfamethoxazole and Bisphenol A from Contaminated Water using Functionalized Carbonaceous Material Derived from Tea Leaves. Issue 4 (August 2018)

• Record Type: Journal Article
• Authors: Ahsan, Md Ariful; Islam, Md Tariqul; Hernandez, Cesar; Kim, Hoejin; Lin, Yirong; Curry, Michael L.; Gardea-Torresdey, Jorge; Noveron, Juan C.
• Is Part Of: Journal of environmental chemical engineering. Volume 6:Issue 4(2018)
• Page Start: 4215
• Page End: 4225
• Publication Date: 2018-08
• Subjects: Adsorption -- Bisphenol A -- Carbonaceous material -- Sulfonation -- Tea leaves -- Sulfamethoxazole; Chemical engineering -- Environmental aspects -- Periodicals; Environmental engineering -- Periodicals; Chemical engineering -- Environmental aspects; Environmental engineering; Periodicals; 660.0286
• DOI: 10.1016/j.jece.2018.06.022
• Languages: English
• ISSNs: 2213-2929

Abstract

Abstract: In this study, we report a facile method for the preparation of sulfonic acid functionalized carbonaceous adsorbent (TW-SO3 H) from tea leaves. The adsorbent was characterized using Fourier-transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Energy-dispersive X-ray Spectroscopy (EDS), Thermogravimetric analysis (TGA), Raman Spectroscopy and Zeta potential measurements. The adsorbent was utilized for the adsorptive removal of antibiotics such as sulfamethoxazole (SMX) and endocrine disrupting chemicals such as bisphenol A (BPA) from water. The calculated adsorption capacities of TW-SO3 H were 258.87 mg/g and 236.80 mg/g towards the removal of SMX and BPA, respectively at 25 °C. The new adsorbent has the ability to form electrostatic interaction and π–π stacking that allow the efficient adsorption of SMX and BPA. The Langmuir and Temkin isotherm models best fit the experimental data for the BPA and SMX adsorption processes, respectively. The results of the kinetic studies showed that the removal of SMX and BPA by TW-SO3 H followed pseudo-second order kinetic model. A thermodynamic study indicated that the adsorption process was spontaneous as well as exothermic. The adsorbent was facilely regenerated and recycled for three cycles with a nominal loss of adsorption capacity. Our results indicated that TW-SO3 H could be utilized as a promising adsorbent for the rapid removal of SMX and BPA from the contaminated water.