Intercalating negatively charged pillars into graphene oxide sheets to enhance sulfonamide pharmaceutical removal from water

被引:4
作者
Wang, Wei [1 ]
Wang, Shiyi [1 ]
Vakili, Mohammadtaghi [2 ]
Wang, Yan [1 ]
Sun, Chang [1 ]
Yang, Haoru [3 ]
Xiao, Guotao [1 ]
Gong, Minjuan [1 ]
Zhou, Shuangxi [1 ]
机构
[1] Qinghai Univ, State Key Lab Plateau Ecol & Agr, Xining 810016, Qinghai, Peoples R China
[2] Yangtze Normal Univ, Green Intelligence Environm Sch, Chongqing 408100, Peoples R China
[3] Colorado Coll, Colorado Springs, CO 80903 USA
关键词
Graphene oxide; Rigid molecules; Sulfadiazine; Density functional theory; PPCPs; POROUS CARBON; ADSORPTION; ANTIBIOTICS; SULFAMETHAZINE; NANOSHEETS; BIOCHAR; DYE;
D O I
10.1007/s11356-022-20949-w
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Herein, novel composite materials were prepared by intercalating functional pillars, i.e., pentafluorobenzene (PFB) and sodium 2,3,4,5,6-pentafluorobenzoate (PFBS), into graphene oxide (GO) sheets. It led to forming size hives and increased availability of intrinsic area of GO. The synthesized materials (GO-PFB and GO-PFBS) were investigated as adsorbents to eliminate sulfadiazine (SD) from aqueous solutions. The adsorption capacities of GO-PFBS (1002.21 mu mol/g) and GO-PFB (564.17 mu mol/g) were 6.37 and 3.59 times higher than that of GO (157.21 mu mol/g), respectively. The adsorption of SD onto GO-PFBS decreased with increasing solution pH. Density functional theory (DFT) results revealed that the SD adsorption onto the adsorbents was exothermic, and the introduction of the carboxylate groups showed lower binding energy. It was found that hydrophobic interaction fully participates in the adsorption process, and the electrostatic complementation of hydrogen bonding further enhances the SD adsorption. Obtained results showed that intercalating functional rigid molecules as pillars to support GO sheets could improve its adsorption behavior.
引用
收藏
页码:72545 / 72555
页数:11
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