Green synthesis of the copper and iron phthalocyanine-based metal–organic framework as an efficient catalyst for methylene blue dye degradation and oxidation of cyclohexane

Literature Information

Publication Date 2023-08-22
DOI 10.1039/D3RE00343D
Impact Factor 4.239
Authors

Rupali S. Bhise, Yogesh A. Patil, Ganapati S. Shankarling


View Original

Abstract

We have successfully developed a simple, energy-efficient, and environmentally benign synthesis method for iron phthalocyanine (FePc) and a MOF based on copper under ambient conditions in water. The synthesized Cu–FePc MOF has been thoroughly characterized using various techniques, including PXRD, FTIR, SEM, TGA and BET. The catalytic activity of the synthesized Cu–FePc MOF was tested in two reactions: (a) oxidative dye degradation of methylene blue using H2O2 and (b) oxidation of cyclohexane to cyclohexanone using TBHP under mild reaction conditions. The catalyst showed excellent performance, as 10 mg of Cu–FePc MOF was able to degrade 20 ml of 40 ppm dye solution in just 16 min. Additionally, it achieved 96% conversion of cyclohexane to cyclohexanone in 3 h. The effect of various parameters such as initial pH, temperature, catalyst loading, and the concentration of H2O2 and TBHP on the catalyst's performance was investigated to optimize the reaction conditions. The Cu–FePc MOF demonstrated excellent recyclability without much loss in its catalytic activity.

Related Literature

The interaction of H2S with the ZnO(100) surface

Jakub Goclon, Bernd Meyer

2013-04-26 Paper

DOI: 10.1039/C3CP44546A

Tandem cathode for proton exchange membrane fuel cells

Samira Siahrostami, Mårten E. Björketun, Peter Strasser, Jeff Greeley, Jan Rossmeisl

2013-04-22 Paper

DOI: 10.1039/C3CP51479J

Surface modification imparts selectivity, facilitating redox catalytic studies: quinone mediated oxygen reduction

Joseph Mason, Christopher Batchelor-McAuley, Richard G. Compton

2013-04-22 Paper

DOI: 10.1039/C3CP50607J

Model of the photoexcitation processes of a two-level molecule coherently coupled to an optical antenna

Masatoshi Nakatani, Atsushi Nobuhiro, Nobuhiko Yokoshi, Hajime Ishihara

2013-03-18 Paper

DOI: 10.1039/C3CP43834A

Spectral assignments and NMR parameter–structure relationships in borates using high-resolution 11B NMR and density functional theory

Oliver L. G. Alderman, Dinu Iuga, Andrew P. Howes, Diane Holland, Ray Dupree

2013-04-05 Paper

DOI: 10.1039/C3CP50772F

The impact of spectator species on the interaction of H2O2 with platinum – implications for the oxygen reduction reaction pathways

Ioannis Katsounaros, Josef C. Meier, Udo Benedikt, P. Ulrich Biedermann, Angel Cuesta, Alexander A. Auer, Karl J. J. Mayrhofer

2013-03-01 Paper

DOI: 10.1039/C3CP50649E

A variable temperature synchrotron X-ray diffraction study of the ferroelastic double perovskite Ba2GdMoO6

Thomas K. Wallace, Ross H. Colman, Abbie C. Mclaughlin

2013-01-03 Paper

DOI: 10.1039/C2CP43732E

Controlled electrochemical deposition and transformation of hetero-nanoarchitectured electrodes for energy storage

Jonathon Duay, Eleanor Gillette, Junkai Hu

2013-04-17 Perspective

DOI: 10.1039/C3CP50724F

Atomic pair distribution functions analysis of disordered low-Z materials

V. Petkov, Y. Ren, S. Kabekkodu, D. Murphy

2012-12-13 Paper

DOI: 10.1039/C2CP43378H

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

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.