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Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type

[Image: see text] The application of solid electrolyte reactors for methane oxidation to co-generation of power and chemicals could be interesting, mainly with the use of materials that could come from renewable sources and abundant metals, such as the [6,6′- (2, 2′-bipyridine-6, 6′-diyl)bis (1,3,5-...

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Autores principales: Garcia, Luis M. S., Rajak, Sanil, Chair, Khaoula, Godoy, Camila M., Silva, Araceli Jardim, Gomes, Paulo V. R., Sanches, Edgar Aparecido, Ramos, Andrezza S., De Souza, Rodrigo F. B., Duong, Adam, Neto, Almir O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346244/
https://www.ncbi.nlm.nih.gov/pubmed/32656421
http://dx.doi.org/10.1021/acsomega.0c01363
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author Garcia, Luis M. S.
Rajak, Sanil
Chair, Khaoula
Godoy, Camila M.
Silva, Araceli Jardim
Gomes, Paulo V. R.
Sanches, Edgar Aparecido
Ramos, Andrezza S.
De Souza, Rodrigo F. B.
Duong, Adam
Neto, Almir O.
author_facet Garcia, Luis M. S.
Rajak, Sanil
Chair, Khaoula
Godoy, Camila M.
Silva, Araceli Jardim
Gomes, Paulo V. R.
Sanches, Edgar Aparecido
Ramos, Andrezza S.
De Souza, Rodrigo F. B.
Duong, Adam
Neto, Almir O.
author_sort Garcia, Luis M. S.
collection PubMed
description [Image: see text] The application of solid electrolyte reactors for methane oxidation to co-generation of power and chemicals could be interesting, mainly with the use of materials that could come from renewable sources and abundant metals, such as the [6,6′- (2, 2′-bipyridine-6, 6′-diyl)bis (1,3,5-triazine-2, 4-diamine)](nitrate-O)copper (II) complex. In this study, we investigated the optimal ratio between this complex and carbon to obtain a stable, conductive, and functional reagent diffusion electrode. The most active Cu-complex compositions were 2.5 and 5% carbon, which were measured with higher values of open circuit and electric current, in addition to the higher methanol production with reaction rates of 1.85 mol L(–1) h(–1) close to the short circuit potential and 1.65 mol L(–1) h(–1) close to the open circuit potential, respectively. This activity was attributed to the ability of these compositions to activate water due to better distribution of the Cu complex in the carbon matrix as observed in the rotating ring disk electrode experiments.
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spelling pubmed-73462442020-07-10 Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type Garcia, Luis M. S. Rajak, Sanil Chair, Khaoula Godoy, Camila M. Silva, Araceli Jardim Gomes, Paulo V. R. Sanches, Edgar Aparecido Ramos, Andrezza S. De Souza, Rodrigo F. B. Duong, Adam Neto, Almir O. ACS Omega [Image: see text] The application of solid electrolyte reactors for methane oxidation to co-generation of power and chemicals could be interesting, mainly with the use of materials that could come from renewable sources and abundant metals, such as the [6,6′- (2, 2′-bipyridine-6, 6′-diyl)bis (1,3,5-triazine-2, 4-diamine)](nitrate-O)copper (II) complex. In this study, we investigated the optimal ratio between this complex and carbon to obtain a stable, conductive, and functional reagent diffusion electrode. The most active Cu-complex compositions were 2.5 and 5% carbon, which were measured with higher values of open circuit and electric current, in addition to the higher methanol production with reaction rates of 1.85 mol L(–1) h(–1) close to the short circuit potential and 1.65 mol L(–1) h(–1) close to the open circuit potential, respectively. This activity was attributed to the ability of these compositions to activate water due to better distribution of the Cu complex in the carbon matrix as observed in the rotating ring disk electrode experiments. American Chemical Society 2020-06-25 /pmc/articles/PMC7346244/ /pubmed/32656421 http://dx.doi.org/10.1021/acsomega.0c01363 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Garcia, Luis M. S.
Rajak, Sanil
Chair, Khaoula
Godoy, Camila M.
Silva, Araceli Jardim
Gomes, Paulo V. R.
Sanches, Edgar Aparecido
Ramos, Andrezza S.
De Souza, Rodrigo F. B.
Duong, Adam
Neto, Almir O.
Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title_full Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title_fullStr Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title_full_unstemmed Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title_short Conversion of Methane into Methanol Using the [6,6′-(2,2′-Bipyridine-6,6′-Diyl)bis(1,3,5-Triazine-2,4-Diamine)](Nitrato-O)Copper(II) Complex in a Solid Electrolyte Reactor Fuel Cell Type
title_sort conversion of methane into methanol using the [6,6′-(2,2′-bipyridine-6,6′-diyl)bis(1,3,5-triazine-2,4-diamine)](nitrato-o)copper(ii) complex in a solid electrolyte reactor fuel cell type
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346244/
https://www.ncbi.nlm.nih.gov/pubmed/32656421
http://dx.doi.org/10.1021/acsomega.0c01363
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