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新型活性炭从水溶液中去除药物化合物,该活性炭由梯牧草(禾本科)合成。

Removal of pharmaceutical compounds from aqueous solution by novel activated carbon synthesized from lovegrass (Poaceae).

机构信息

Postgraduate Program in Engineering, Federal University of Pampa (UNIPAMPA), Bagé, RS, 96412-420, Brazil.

Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.

出版信息

Environ Sci Pollut Res Int. 2020 Jun;27(17):21442-21454. doi: 10.1007/s11356-020-08617-3. Epub 2020 Apr 10.

DOI:10.1007/s11356-020-08617-3
PMID:32277415
Abstract

In this work, lovegrass (Cpa), an abundant grass of the Poaceae family, was employed as feedstock for the production of activated carbon in a conventional furnace using ZnCl as a chemical activator. The prepared material (Cpa-AC) was characterized by pH of the point of zero charges (pH), Boehm's titration method, CHN/O elemental analysis, ATR-FTIR, N adsorption/desorption curves, and SEM. This carbon material was used for adsorption of acetylsalicylic acid (ASA) and sodium diclofenac (DFC). FTIR analysis identified the presence of O-H, N-H, O-C=O), C-O, and aromatic ring bulk and surface of (Cpa-AC) adsorbent. The quantification of the surface functional groups showed the presence of a large amount of acidic functional groups on the surface of the carbon material. The isotherms of adsorption and desorption of N confirm that the Cpa-AC adsorbent is mesopore material with a large surface area of 1040 m g. SEM results showed that the surface of Cpa-AC is rugous. The kinetic study indicates that the system followed the pseudo-second-order model (pH 4.0). The equilibrium time was achieved at 45 (ASA) and 60 min (DCF). The Liu isotherm model best fitted the experimental data. The maxima sorption capacities (Q) for ASA and DFC at 25 °C were 221.7 mg g and 312.4 mg g, respectively. The primary mechanism of ASA and DFC adsorption was justified considering electrostatic interactions and π-π interactions between the Cpa-AC and the adsorbate from the solution.

摘要

在这项工作中,我们使用禾本科的拉拉草(Cpa)作为原料,在常规炉中使用 ZnCl2 作为化学活化剂生产活性炭。通过 pH 滴定法、Boehm 滴定法、CHN/O 元素分析、ATR-FTIR、N2 吸附/解吸曲线和 SEM 对制备的材料(Cpa-AC)进行了表征。该碳材料用于吸附乙酰水杨酸(ASA)和双氯芬酸钠(DFC)。FTIR 分析表明,(Cpa-AC)吸附剂表面存在 O-H、N-H、O-C=O)、C-O 和芳环体。表面官能团的定量分析表明,碳材料表面存在大量酸性官能团。N 的吸附和解吸等温线证实 Cpa-AC 吸附剂是具有 1040 m2/g 大表面积的中孔材料。SEM 结果表明,Cpa-AC 的表面是粗糙的。动力学研究表明,该体系遵循准二级模型(pH 4.0)。在 45 分钟(ASA)和 60 分钟(DFC)时达到平衡时间。Liu 等温线模型最适合实验数据。在 25°C 下,ASA 和 DFC 的最大吸附容量(Q)分别为 221.7mg/g 和 312.4mg/g。从溶液中考虑静电相互作用和 Cpa-AC 与吸附质之间的π-π相互作用,证明了 ASA 和 DFC 吸附的主要机制。

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