3D construction of a cobalt(ii) coordination polymer as a photocatalyst for the degradation of methyl green dye under visible light and its mechanistic pathway

Literature Information

Publication Date 2023-11-29
DOI 10.1039/D3NJ03938B
Impact Factor 3.591
Authors

Rais Ahmad Khan, Amal AlFawaz, Afnan Abdullah Alhamed, Nouf Abdulrahman AlMuryyi, Imran Hasan, Anup Paul, Sandeep Dey, Saad. G. Alshammari, Hadi D. Arman, Ali Alsalme


View Original

Abstract

A new cobalt(II) coordination polymer ‘Cp-Co’ has been designed and synthesized. The construction includes cobalt(II) as the central metal core along with 1,4-benzenedicarboxylic acid and the spacer 3,5-diamino-1,2,4-triazole obtained by a solvothermal method. The architecture of ‘Cp-Co’ was established using single X-ray crystallography and the topology of the coordination polymer. The ‘Cp-Co’ exhibited a periodic 3D framework. Furthermore, infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and Brunauer–Emmett–Teller (BET) analysis further supported the structure of ‘Cp-Co’. The prepared material was explored as a catalyst for the photocatalytic degradation of methyl green (MG) dye and displayed outstanding degradation efficiency under visible light radiation. The experimental design was explored towards optimization of the reaction variables, such as catalyst dose, MG dye concentration, etc. It was found that 10 mg of Cp-Co with 150 mg L−1 MG resulted in 99.77% photocatalytic efficiency within 60 min of visible light irradiation. The kinetic data was simulated using the Langmuir–Hinshelwood kinetic model and the value of the apparent rate constant (Kapp) was found to be 0.020 min−1, 0.024 min−1 and 0.029 min−1 for 50, 100 and 150 mg L−1 MG concentrations. The trapping experiments suggested the involvement of a superoxide anion radical (O2−˙) in the degradation of MG.

Related Literature

A new type of nonsulfide hydrotreating catalyst: nickel phosphide on carbon

Yuying Shu, S. Ted Oyama

2005-01-12 Communication

DOI: 10.1039/B415838E

Reversible and irreversible conformational changes in poly(isocyanide)s: a remote stereoelectronic effect

David B. Amabilino, José-Luis Serrano, Jaume Veciana

2004-12-08 Communication

DOI: 10.1039/B411449C

Encapsulated sulfates: insight to binding propensities

Sung Ok Kang, Md. Alamgir Hossain, Douglas Powell, Kristin Bowman-James

2004-11-29 Communication

DOI: 10.1039/B411904E

Direct quantitative determination of surface Brønsted acidity of solids by H/D exchange using D2O

Nicolas Keller, Guillaume Koehl, François Garin, Valérie Keller

2004-12-06 Communication

DOI: 10.1039/B412242A

A pyrimidine-like nickel(ii) DNA base pair

Christopher Switzer, Dongwon Shin

2005-01-19 Communication

DOI: 10.1039/B415426F

Nanocrystalline and mesostructured Y2O3 as supports for gold catalysts

Javier Guzman, Avelino Corma

2004-12-14 Communication

DOI: 10.1039/B413338B

Inversion of enantioselectivity of asymmetric biocatalytic decarboxylation by site-directed mutagenesis based on the reaction mechanism

Yoichiro Ijima, Kaori Matoishi, Yosuke Terao, Nobuhide Doi, Hiroshi Yanagawa, Hiromichi Ohta

2005-01-10 Communication

DOI: 10.1039/B416398B

Direct mono-insertion of isocyanides into terminal alkynes catalyzed by rare-earth silylamides

Kimihiro Komeyama, Daisuke Sasayama, Tomonori Kawabata, Katsuomi Takehira, Ken Takaki

2004-12-13 Communication

DOI: 10.1039/B414302G

A small peptide stereochemically customized as a globular fold with a molecular cleft

Soumendra Rana, Bijoy Kundu, Susheel Durani

2004-11-17 Communication

DOI: 10.1039/B413802C

You might also like

Compound Q&A

What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?

When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...

79206-94-34-(2-Furylmethyl)thi...
Compound Q&A

What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?

When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...

71320-77-94-Chloro-N-[2-(4-mor...
Compound Q&A

How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?

Waste containing this compound (CAS: 62921-74-8) should be handled according to ...

62921-74-82-[2-(2-Methoxyethox...
Compound Q&A

How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?

Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...

40056-18-6(S)-Methyl 2-amino-3...
166882-70-85-({4-[(2S,4R)-4-Hyd...
Compound Q&A

Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?

There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...

7312-27-8(2E)-3-(3,4-Dichloro...
Compound Q&A

How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?

Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...

925437-84-9Ethyl 6-(2-nitrophen...
Compound Q&A

How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?

Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...

18453-07-12-(1,3-Thiazol-2-yl)...
Compound Q&A

How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?

Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...

103440-54-6Methyl 5-iodo-2-meth...
Compound Q&A

How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?

5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...

1427399-34-55-Chloro[1,2,4]triaz...

Source Journal

New Journal of Chemistry

New Journal of Chemistry
CiteScore: 5.3
Self-citation Rate: 3.7%
Articles per Year: 2153

NJC (New Journal of Chemistry) is a broad-based primary journal encompassing all branches of chemistry and its sub-disciplines. It contains full research articles, communications, perspectives and focus articles. This well-established journal, owned by the Centre National de la Recherche Scientifique (CNRS) of France, has been co-published with the Royal Society of Chemistry since January 1998. NJC is the forum for the publication of high-quality, original and significant work that opens new directions in chemistry or other scientific disciplines. In addition to having a significant chemical component, work published in NJC must demonstrate that it will have an impact on areas of research other than that of the reported work.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.