Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 8, Issue 22, Pages 11362-11369Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta01847c
Keywords
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Funding
- National Natural Science Foundation of China [21876172, 21906073, 11675210, 21976089]
- Natural Science Foundation of Gansu Province [17JR5RA309]
- West Light Foundation of The Chinese Academy of Sciences
- Key Laboratory Project of Gansu Province [1309RTSA041]
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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.
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