4.7 Article

Facile fabrication of phenylenediamine residue derived N, O co-doped hierarchical hyperporous carbon for high-efficient chloroxylenol removal

期刊

CHEMICAL ENGINEERING JOURNAL
卷 433, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.133635

关键词

Hierarchical hyperporous carbon; Chloroxylenol; Adsorption; DFT calculation; N/O co-doped

资金

  1. National Natural Science Founda-tion of China [22108144]
  2. Primary Research & Development Plan of Shandong Province [2019GSF109055]
  3. Postdoctoral Application Research Project of Qingdao

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In this study, a hierarchical hyperporous carbon material (HHPC) was synthesized using a carbonization-casting-activation strategy, achieving in-situ N/O co-doping. The HHPC exhibited high specific surface area and remarkable adsorption capacity for chloroxylenol, and showed excellent reusability and tolerance under various conditions.
The chloroxylenol (PCMX) has shown well virucidal efficacy against COVID-19, but the large-scale utilization of which will undoubtedly pose extra environmental threaten. In the present study, the recycled industrial phenylenediamine residue was used and an integrated strategy of carbonization-casting-activation using super low-dose of activator and templates was established to achieve in-situ N/O co-doping and facile synthesis of a kind of hierarchical hyperporous carbons (HHPC). The sample of HHPC-1.25-0.5 obtained with activator and template to residue of 1.25 and 0.5 respectively shows super-high specific surface area of 3602 m(2)/g and volume of 2.81 cm(3)/g and demonstrates remarkable adsorption capacity of 1475 mg/g for PCMX in batch and of 1148 mg/g in dynamic column adsorption test. In addition, the HHPC-1.25-0.5 exhibits excellent reusability and tolerance for PCMX adsorption under various ionic backgrounds and real water matrix conditions. The combined physio-chemistry characterization, kinetic study and DFT calculation reveal that the enhanced high performances originate from the hierarchical pore structure and strong electrostatic interaction between PCMX and surface rich pyridinic-N and carbonyl groups.

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