Mesoporous Biphasic C and N Codoped Anatase Nanocrystal–Carbon Composites and their Derived Doped Anatase Nanoparticles in Phenol Elimination under Visible Light. Issue 18 (14th July 2015)
- Record Type:
- Journal Article
- Title:
- Mesoporous Biphasic C and N Codoped Anatase Nanocrystal–Carbon Composites and their Derived Doped Anatase Nanoparticles in Phenol Elimination under Visible Light. Issue 18 (14th July 2015)
- Main Title:
- Mesoporous Biphasic C and N Codoped Anatase Nanocrystal–Carbon Composites and their Derived Doped Anatase Nanoparticles in Phenol Elimination under Visible Light
- Authors:
- Zhu, Xiaojuan
Wei, Wei
Wan, Ying - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Mesoporous C and N codoped anatase nanocrystal–carbon composites have been synthesized by chelation‐assisted coassembly of urea, TiCl<sub>4</sub>, resols, and triblock copolymer. The composite catalysts have biphasic constituents in the pore walls of amorphous carbon and C, N‐codoped anatase nanoparticles (≈4.0 nm) that are "glued" together; the composite catalysts also have open mesopores with high surface areas (≈340 m<sup>2</sup> g<sup>−1</sup>), large pore volumes (≈0.20 cm<sup>3</sup> g<sup>−1</sup>), and uniform pore sizes (≈5.0 nm). Upon calcination in air at 350 °C, the main‐group‐elements‐codoped anatase nanoparticles with a size of 4.3 nm can be obtained. The C, N‐codoped anatase nanoparticles feature a clear redshift absorption towards the visible‐light region and exhibit remarkable degradation efficiency for phenol. A repeated accumulation–photodegradation process is adopted to remove high concentrations of phenol (100 mg L<sup>−1</sup>) from water, thereby avoiding the use of organic solvent and the posttreatment of the catalyst. After six cycles, phenol is almost completely degraded. The features of the two constituents of the composite are discussed. The mesoporous carbon support shows a high adsorption capacity for phenol, which accumulates inside its pores, and the main‐group‐elements‐doped anatase nanoparticles can be well accessible to phenol, which it mineralizes under artificial<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Mesoporous C and N codoped anatase nanocrystal–carbon composites have been synthesized by chelation‐assisted coassembly of urea, TiCl<sub>4</sub>, resols, and triblock copolymer. The composite catalysts have biphasic constituents in the pore walls of amorphous carbon and C, N‐codoped anatase nanoparticles (≈4.0 nm) that are "glued" together; the composite catalysts also have open mesopores with high surface areas (≈340 m<sup>2</sup> g<sup>−1</sup>), large pore volumes (≈0.20 cm<sup>3</sup> g<sup>−1</sup>), and uniform pore sizes (≈5.0 nm). Upon calcination in air at 350 °C, the main‐group‐elements‐codoped anatase nanoparticles with a size of 4.3 nm can be obtained. The C, N‐codoped anatase nanoparticles feature a clear redshift absorption towards the visible‐light region and exhibit remarkable degradation efficiency for phenol. A repeated accumulation–photodegradation process is adopted to remove high concentrations of phenol (100 mg L<sup>−1</sup>) from water, thereby avoiding the use of organic solvent and the posttreatment of the catalyst. After six cycles, phenol is almost completely degraded. The features of the two constituents of the composite are discussed. The mesoporous carbon support shows a high adsorption capacity for phenol, which accumulates inside its pores, and the main‐group‐elements‐doped anatase nanoparticles can be well accessible to phenol, which it mineralizes under artificial visible light. Simultaneously, the "glue" role of the amorphous carbon can overcome the disadvantages of possible particle aggregation during processes and allow the catalyst to be reused.</p> </abstract> … (more)
- Is Part Of:
- ChemCatChem. Volume 7:Issue 18(2015:Sep.)
- Journal:
- ChemCatChem
- Issue:
- Volume 7:Issue 18(2015:Sep.)
- Issue Display:
- Volume 7, Issue 18 (2015)
- Year:
- 2015
- Volume:
- 7
- Issue:
- 18
- Issue Sort Value:
- 2015-0007-0018-0000
- Page Start:
- 2945
- Page End:
- 2956
- Publication Date:
- 2015-07-14
- Subjects:
- Catalysis -- Periodicals
541.39505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cctc.201500341 ↗
- Languages:
- English
- ISSNs:
- 1867-3880
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4050.xml