Efficiency and active sites of the synergetic sorption and photocatalysis in Cr(vi) decontamination on a 3D oxidized graphene ribbon framework

被引:45
作者
Ding, Zhe [1 ,2 ,3 ]
Liang, Jianjun [1 ,2 ]
Zhang, Wentao [1 ,2 ,3 ]
Wang, Wei [1 ,2 ,3 ]
Geng, Rongyue [1 ,2 ,3 ]
Wang, Yun [1 ,2 ,3 ]
Li, Ping [1 ,2 ]
Fan, Qiaohui [1 ,2 ]
机构
[1] Chinese Acad Sci, Northwest Inst Ecoenvironm & Resources, Lanzhou 730000, Peoples R China
[2] Key Lab Petr Resources, Lanzhou 730000, Gansu, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 中国科学院西部之光基金;
关键词
VIBRATIONAL-SPECTRA; CARBON NANOTUBES; GRAPHITE OXIDE; REDUCTION; CHROMIUM; ADSORPTION; EVOLUTION; HYDROGEL; KINETICS; REMOVAL;
D O I
10.1039/d0ta01847c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synergetic effect of sorption and photocatalysis for metal sequestration promises unique advantages in environmental remediation; however, the mechanism, especially with regard to the photocatalytic sites, is still ambiguous in carbon catalysts. Here, a metal-free three-dimensional carbon framework, named P-OGR, was fabricatedviathe assembly of oxidized graphene ribbons (OGRs) and polyacrylamide (PA). In the dark, the sorption capacity of Cr(vi) on P-OGR achieved 338.2 mg g(-1)within 2 min. In sunlight for 5 days, P-OGR could immobilize and photo-reduce 687.8 mg g(-1)of Cr(vi) into Cr(2)O(3)nanospheres. The active sites on P-OGR were exploredviamodeling experiments. In the sorption, -NH(3)(+)was the best site due to the electrostatic attraction with Cr(vi) anions. Hydroxyls, followed by carboxyl groups, enabled weak hydrogen bonding to capture Cr(vi). During the photocatalysis, the activities of the catalytic sites were evaluated as follows: carboxyl > hydroxyl > ketone > aldehyde, which were consistent with their Lewis acidities.
引用
收藏
页码:11362 / 11369
页数:8
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