Faculty of Environmental Science & Engineering, Kunming University of Science & Technology, Kunming 650500, PR China.
Faculty of Environmental Science & Engineering, Kunming University of Science & Technology, Kunming 650500, PR China.
Sci Total Environ. 2018 Mar 15;618:269-275. doi: 10.1016/j.scitotenv.2017.11.065. Epub 2017 Nov 10.
The dominant adsorption mechanism of ionizable organic chemicals (IOCs) on carbonaceous materials is still unclear. This study used benzoic acid (BA), o-chlorobenzoic acid (2-CBA) and p-chlorobenzoic acid (4-CBA) as representatives of IOCs to investigate the dominant adsorption mechanism on graphene oxide (GO) and graphite (GP), with a specific emphasis on the impact of pH-dependent K. The order of apparent adsorption of the investigated chemicals changed with pH, which could not be explained by their constant K. According to our measurement, K varied greatly with pH. The pH-dependent adsorption of BA, 2-CBA and 4-CBA were significantly correlated with pH-dependent K for both GO and GP. Our observations indicated that the hydrophobic effects may dominate the apparent adsorption of BA, 2-CBA and 4-CBA on GO and GP. Electrostatic repulsion played a minor role in their reduced adsorption at high pH. Negative charge-assisted H-bond and π-π interactions may explain the adsorption of negatively charged BA, 2-CBA and 4-CBA on negatively charged GO. This study implied that pH-dependent K rather than constant K should be incorporated to understand IOC adsorption as affected by pH.
离子化有机化学品(IOCs)在碳质材料上的主要吸附机制仍不清楚。本研究选用苯甲酸(BA)、邻氯苯甲酸(2-CBA)和对氯苯甲酸(4-CBA)作为 IOCs 的代表,研究其在氧化石墨烯(GO)和石墨(GP)上的主要吸附机制,特别关注 pH 依赖性 K 的影响。研究化学品的表观吸附顺序随 pH 而变化,这不能用其常数 K 来解释。根据我们的测量,K 值随 pH 值变化很大。BA、2-CBA 和 4-CBA 的 pH 依赖性吸附与 GO 和 GP 上的 pH 依赖性 K 显著相关。我们的观察表明,疏水力可能主导 BA、2-CBA 和 4-CBA 在 GO 和 GP 上的表观吸附。在高 pH 值下,静电排斥在它们的吸附减少中作用较小。负电荷辅助氢键和π-π相互作用可以解释带负电荷的 BA、2-CBA 和 4-CBA 在带负电荷的 GO 上的吸附。本研究表明,应该结合 pH 依赖性 K 而不是常数 K 来理解 pH 影响下的 IOC 吸附。