期刊
APPLIED SURFACE SCIENCE
卷 552, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apsusc.2021.149513
关键词
Adsorption; Carbon-based adsorbents; Endocrine disruptor; Kraft lignin; Surface chemistry
类别
资金
- Spanish MICINN [CTM2017-84033-R]
- Regional Government of Madrid [IND2017/AMB-7720, S2018/EMT-4341]
- European Social Fund
- Associate Laboratory LSRE-LCM - national funds through FCT/MCTES (PIDDAC) [UIDB/50020/2020]
Carbon-based adsorbents were tested for BPA adsorption from water, with modified materials showing enhanced adsorption capacity after treatments, especially high-temperature treatment leading to a 73% increase in adsorption capacity. The correlation between micropore volume, specific surface area, and BPA adsorption capacity was observed, with chemisorption identified as the dominant sorption mechanism.
Carbon-based adsorbents, e.g., xerogel (RFX) and lignin-based activated carbon (KLP) were characterized and tested for the adsorption of the endocrine disrupting compound Bisphenol A (BPA) from water. Then, pristine materials were modified following mechanical, chemical and thermal treatments. Pristine RFX showed a moreopened porous structure, enhancing the adsorption kinetic, c.a. 24 vs. 48 h equilibrium time, for RFX and KLP samples, respectively. Thus, RFX adsorption capacity decreased in comparison to that obtained for KLP (qsat = 78 vs 220 mg g-1). Thus, a clear correlation between micropore volume (Vmicro) and specific surface area (SBET) with BPA adsorption capacity could be established; so, an increment of BPA adsorption capacity was observed with an increase in both textural parameters. Moreover, the dominant sorption mechanism seems to be chemisorption; and DSL isotherm model was found the most suitable for the fitting of BPA adsorption isotherms. Generally, the presence of oxygenated/nitrogenated-groups on carbon surface led to a decrease in BPA adsorption capacity due to the decrease in 7C-7C dispersive interactions and pore blocking phenomena. Finally, an increment in BPA adsorption capacity up to 135 mg g-1 (73% higher than that obtained for the pristine material) was obtained with the sample treated at high temperature.
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