期刊
JOURNAL OF HAZARDOUS MATERIALS
卷 391, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jhazmat.2020.122163
关键词
Triazine-formaldehyde phenolic resin; N-doped mesoporous carbon; Block copolymer; CO(2)uptake; Organic dye adsorption
资金
- Ministry of Science and Technology, Taiwan [MOST 106-2221-E-110-067MY3, 108-2638-E-002-003-MY2, 108-2218-E-110-013-MY3, 1082221-E-110-014-MY3]
In this study we synthesized a triazine-formaldehyde phenolic resin as a nitrogen-containing resol (N-resol) through the condensation of 2,4,6-tris(4-hydroxyphenyl)triazine and formaldehyde. We then used this N-resol as a carbon and nitrogen atom source, mixing it with a diblock copolymer of PEO-b-PCL as the soft template, for the direct synthesis of N-doped mesoporous carbons. Interestingly, the self-assembled N-resol/PEO-b-PCL blends underwent a mesophase transition from cylinder to gyroid and back again to cylinder structures upon increasing the N-resol concentration (i.e., cylinder at 50/50; gyroid at 60/40; cylinder at 70/30). After removing the soft template at 700 degrees C, the resultant N-doped mesoporous carbons possessed high N atom contents (up to 13 wt%) and displayed gyroid and cylinder nanostructures. The synthesized N-doped mesoporous carbons exhibited excellent CO2 uptake capacities (up to 72 and 150 mg g(-1) at 298 and 273 K, respectively). Furthermore, the N-doped mesoporous gyroid carbon structure displayed high adsorption capacities toward organic dyes in water. The maximum adsorption capacities of rhodamine B and methylene blue in water reached as high as 204.08 and 308.64 mg g(-1), respectively; furthermore, these N-doped mesoporous carbons also maintained up to 98 % of their maximum adsorption capacities within 45 min.
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