Fe/Mn nanoparticles encapsulated in nitrogen-doped carbon nanotubes as a peroxymonosulfate activator for acetamiprid degradation
N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for peroxymonosulfate activation to degrade acetamiprid. The FeMn@NCNTs showed uniform nanotubes with rich N doping and the encapsulated FeMn na...
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Published in | Environmental science. Nano Vol. 6; no. 6; pp. 1799 - 1811 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
13.06.2019
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Abstract | N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for peroxymonosulfate activation to degrade acetamiprid. The FeMn@NCNTs showed uniform nanotubes with rich N doping and the encapsulated FeMn nanoparticles were doubly protected by both NCNTs and a clingy graphitic structure. The results indicated that the confined FeMn nanoparticles were designated as Fe
2.7
Mn
0.3
C according to the XRD pattern and elemental composition. Radical quenching indicated that SO
4
&z.rad;
−
and &z.rad;OH were the dominant radicals in the FeMn@NCNTs/PMS system. The indispensable roles of both radical pathways of O
2
&z.rad;
−
and non-radical
1
O
2
in the superior catalytic performance were also confirmed. As a result, both the embedded FeMn nanoparticles and NCNTs in FeMn@NCNTs contributed to the acetamiprid degradation with multiple degradation mechanisms. XPS results confirmed the formation of redox cycles between the multiple valence states of Mn and Fe, which ensured the superior catalytic activity of FeMn@NCNTs for PMS activation. In addition, only a small decrease in the catalytic performance from 99.5% to 90% was observed after four cycles. The catalytic activity of used FeMn@NCNTs was mostly recovered after heat regeneration (350 °C), which exhibited the excellent stability and reusability of the FeMn@NCNTs.
Bimetallic Fe/Mn nanoparticles and N-doped carbon nanotubes in FeMn@NCNT synergistically activate peroxymonosulfate to form SO
4
&z.rad;
−
, &z.rad;OH, O
2
&z.rad;
−
and
1
O
2
for decomposing acetamiprid. |
---|---|
AbstractList | N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for peroxymonosulfate activation to degrade acetamiprid. The FeMn@NCNTs showed uniform nanotubes with rich N doping and the encapsulated FeMn nanoparticles were doubly protected by both NCNTs and a clingy graphitic structure. The results indicated that the confined FeMn nanoparticles were designated as Fe
2.7
Mn
0.3
C according to the XRD pattern and elemental composition. Radical quenching indicated that SO
4
&z.rad;
−
and &z.rad;OH were the dominant radicals in the FeMn@NCNTs/PMS system. The indispensable roles of both radical pathways of O
2
&z.rad;
−
and non-radical
1
O
2
in the superior catalytic performance were also confirmed. As a result, both the embedded FeMn nanoparticles and NCNTs in FeMn@NCNTs contributed to the acetamiprid degradation with multiple degradation mechanisms. XPS results confirmed the formation of redox cycles between the multiple valence states of Mn and Fe, which ensured the superior catalytic activity of FeMn@NCNTs for PMS activation. In addition, only a small decrease in the catalytic performance from 99.5% to 90% was observed after four cycles. The catalytic activity of used FeMn@NCNTs was mostly recovered after heat regeneration (350 °C), which exhibited the excellent stability and reusability of the FeMn@NCNTs.
Bimetallic Fe/Mn nanoparticles and N-doped carbon nanotubes in FeMn@NCNT synergistically activate peroxymonosulfate to form SO
4
&z.rad;
−
, &z.rad;OH, O
2
&z.rad;
−
and
1
O
2
for decomposing acetamiprid. N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for peroxymonosulfate activation to degrade acetamiprid. The FeMn@NCNTs showed uniform nanotubes with rich N doping and the encapsulated FeMn nanoparticles were doubly protected by both NCNTs and a clingy graphitic structure. The results indicated that the confined FeMn nanoparticles were designated as Fe2.7Mn0.3C according to the XRD pattern and elemental composition. Radical quenching indicated that SO4·− and ·OH were the dominant radicals in the FeMn@NCNTs/PMS system. The indispensable roles of both radical pathways of O2·− and non-radical 1O2 in the superior catalytic performance were also confirmed. As a result, both the embedded FeMn nanoparticles and NCNTs in FeMn@NCNTs contributed to the acetamiprid degradation with multiple degradation mechanisms. XPS results confirmed the formation of redox cycles between the multiple valence states of Mn and Fe, which ensured the superior catalytic activity of FeMn@NCNTs for PMS activation. In addition, only a small decrease in the catalytic performance from 99.5% to 90% was observed after four cycles. The catalytic activity of used FeMn@NCNTs was mostly recovered after heat regeneration (350 °C), which exhibited the excellent stability and reusability of the FeMn@NCNTs. N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for peroxymonosulfate activation to degrade acetamiprid. The FeMn@NCNTs showed uniform nanotubes with rich N doping and the encapsulated FeMn nanoparticles were doubly protected by both NCNTs and a clingy graphitic structure. The results indicated that the confined FeMn nanoparticles were designated as Fe 2.7 Mn 0.3 C according to the XRD pattern and elemental composition. Radical quenching indicated that SO 4 ˙ − and ˙OH were the dominant radicals in the FeMn@NCNTs/PMS system. The indispensable roles of both radical pathways of O 2 ˙ − and non-radical 1 O 2 in the superior catalytic performance were also confirmed. As a result, both the embedded FeMn nanoparticles and NCNTs in FeMn@NCNTs contributed to the acetamiprid degradation with multiple degradation mechanisms. XPS results confirmed the formation of redox cycles between the multiple valence states of Mn and Fe, which ensured the superior catalytic activity of FeMn@NCNTs for PMS activation. In addition, only a small decrease in the catalytic performance from 99.5% to 90% was observed after four cycles. The catalytic activity of used FeMn@NCNTs was mostly recovered after heat regeneration (350 °C), which exhibited the excellent stability and reusability of the FeMn@NCNTs. |
Author | Ma, Tengfei Li, Yanwei Zhang, Xue Zhang, Qingzhu Gao, Baoyu Xu, Xing Yue, Yue Yue, Qinyan Duan, Pijun Shang, Yanan |
AuthorAffiliation | Shandong Key Laboratory of Water Pollution Control and Resource Reuse Shandong University School of Environmental Science and Engineering Environment Research Institute |
AuthorAffiliation_xml | – name: School of Environmental Science and Engineering – name: Environment Research Institute – name: Shandong Key Laboratory of Water Pollution Control and Resource Reuse – name: Shandong University |
Author_xml | – sequence: 1 givenname: Pijun surname: Duan fullname: Duan, Pijun – sequence: 2 givenname: Tengfei surname: Ma fullname: Ma, Tengfei – sequence: 3 givenname: Yue surname: Yue fullname: Yue, Yue – sequence: 4 givenname: Yanwei surname: Li fullname: Li, Yanwei – sequence: 5 givenname: Xue surname: Zhang fullname: Zhang, Xue – sequence: 6 givenname: Yanan surname: Shang fullname: Shang, Yanan – sequence: 7 givenname: Baoyu surname: Gao fullname: Gao, Baoyu – sequence: 8 givenname: Qingzhu surname: Zhang fullname: Zhang, Qingzhu – sequence: 9 givenname: Qinyan surname: Yue fullname: Yue, Qinyan – sequence: 10 givenname: Xing surname: Xu fullname: Xu, Xing |
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Snippet | N-Doped carbon nanotubes encapsulating bimetallic Fe/Mn nanoparticles (FeMn@NCNTs) were fabricated after a one-step pyrolysis and were used as the catalyst for... |
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SubjectTerms | Activation Bimetals Carbon nanotubes Catalysis Catalysts Catalytic activity Chemical composition Cycles Degradation Encapsulation Free radicals Graphitic structure Iron Manganese Nanoparticles Nanotechnology Nanotubes Nitrogen Oxidoreductions Pyrolysis Regeneration Stability Sulphates |
Title | Fe/Mn nanoparticles encapsulated in nitrogen-doped carbon nanotubes as a peroxymonosulfate activator for acetamiprid degradation |
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