Development of a selective, solvent-free epoxidation of limonene using hydrogen peroxide and a tungsten-based catalyst

Literature Information

Publication Date 2018-08-08
DOI 10.1039/C8RE00094H
Impact Factor 4.239
Authors

Ana María López Fernández, Abdul Rehman, Adam P. Harvey


View Original

Abstract

The development of a limonene epoxidation process using environment-friendly H2O2, with high H2O2 conversion (∼95%) and selectivity to the epoxide (100%), is reported in this paper. Parametric studies of temperature, oxidant, solvent, acid concentration and sodium sulphate amounts were performed with the focus on establishing a rapid and highly selective process. Approximately 95% conversion of H2O2 at 100% selectivity to limonene-1,2-epoxide was achieved in 15 minutes with a single-step addition of oxidant. The operating conditions included a 323 K temperature in a solvent-free environment, with a limonene/H2O2/catalyst molar ratio of 4 : 1 : 0.005, using a tungsten-based polyoxometalates. To prevent the hydrolysis of the epoxide, the reaction mixture was saturated with sodium sulphate. An acid concentration of lower than 0.04 M was used and found to have significant effect on the selectivity. Kinetic studies were performed to allow modelling of the reaction scheme. The activation energy was determined to be ∼36 kJ mol−1.

Related Literature

Aqueous emulsion polymerizations of methacrylates and styrene via reversible complexation mediated polymerization (RCMP)

Weijia Mao, Jit Sarkar, Bo Peng, Atsushi Goto

2021-09-28 Paper

DOI: 10.1039/D1PY01087E

Energetically accessible reconstructions along interstitial rows on the rutile (110) surface

Simon D. Elliott, Simon P. Bates

2001-04-30 Communication

DOI: 10.1039/B101804N

Experimental and theoretical study of the recombination reactions of FS(O2)O with FC(O)O and CO

M. E. Tucceri, M. P. Badenes, A. E. Croce, C. J. Cobos

2001-04-23 Paper

DOI: 10.1039/B100348H

Rate coefficients and Arrhenius parameters for the reaction of the NO3 radical with acetaldehyde and acetaldehyde-1d

Barbara D'Anna, Sarka Langer, Evert Ljungström, Claus J. Nielsen, Maria Ullerstam

2001-04-05 Paper

DOI: 10.1039/B100855M

A reinterpretation of the EPR spectra of Cu(II) in zeolites A, Y and ZK4, based on ab initio cluster model calculations

Kristine Pierloot, Annelies Delabie, Marijke H. Groothaert, Robert A. Schoonheydt

2001-04-26 Paper

DOI: 10.1039/B100531F

Quantification of aluminium coordinations in alumina and silica–alumina by Al K-edge XANES

Yuko Kato, Ken-ichi Shimizu, Norimitsu Matsushita, Tomoko Yoshida, Hisao Yoshida, Atsushi Satsuma, Tadashi Hattori

2001-04-20 Paper

DOI: 10.1039/B100610J

Contents list

2021-10-05 Front/Back Matter

DOI: 10.1039/D1PY90128A

You might also like

Compound Q&A

What regulatory guidelines apply to 6-Bromo-2-methylimidazo[1,2-a]pyrimidine (CAS: 1111638-05-1)?

6-Bromo-2-methylimidazo[1,2-a]pyrimidine (CAS: 1111638-05-1) falls under various...

1111638-05-16-Bromo-2-methylimid...
Compound Q&A

Are there alternatives to 1-Pyrrolidineethanol, β-methyl-α-phenyl-, (αS,βR) (CAS: 123620-80-4) in synthesis?

While there are no direct alternatives, similar compounds like 1-Pyrrolidineetha...

123620-80-41-Pyrrolidineethanol...
Compound Q&A

Is 4-Methyl-2,6-bis(2-methyl-2-propanyl)phenyl methylcarbamate (CAS: 1918-11-2) safe?

4-Methyl-2,6-bis(2-methyl-2-propanyl)phenyl methylcarbamate (CAS: 1918-11-2) is ...

1918-11-24-Methyl-2,6-bis(2-m...
Compound Q&A

How should 2-(3-Bromo-4-fluorophenyl)-1,3-dioxolane (CAS: 77771-04-1) be stored?

2-(3-Bromo-4-fluorophenyl)-1,3-dioxolane (CAS: 77771-04-1) should be stored in a...

77771-04-12-(3-Bromo-4-fluorop...
Compound Q&A

What are the physical and chemical properties of 4,5,6,7-Tetrahydro-1H-indazole hydrochloride (CAS: 18161-11-0)?

4,5,6,7-Tetrahydro-1H-indazole hydrochloride is a white crystalline solid with a...

18161-11-04,5,6,7-Tetrahydro-1...
Compound Q&A

What is (2R)-1-Methoxy-3-phenyl-2-propanamine (CAS: 59919-07-2)?

(2R)-1-Methoxy-3-phenyl-2-propanamine is a chiral organic compound with the CAS ...

59919-07-2(2R)-1-Methoxy-3-phe...
Compound Q&A

What industries use Ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate (CAS: 56649-47-9)?

Ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate is used in various industries...

56649-47-9Ethyl 1-(1-phenyleth...
Compound Q&A

What regulatory guidelines apply to 4-[(1E,3S)-1-(4-Hydroxyphenyl)-1,4-pentadien-3-yl]phenol (CAS: 17676-24-3)?

4-[(1E,3S)-1-(4-Hydroxyphenyl)-1,4-pentadien-3-yl]phenol (CAS: 17676-24-3) falls...

17676-24-34-[(1E,3S)-1-(4-Hydr...
Compound Q&A

What industries use (S)-3-Amino-5-phenylpentanoic acid hydrochloride (CAS: 331846-97-0)?

(S)-3-Amino-5-phenylpentanoic acid hydrochloride is primarily used in the pharma...

331846-97-0(S)-3-Amino-5-phenyl...
Compound Q&A

How is 7-methoxy-1-benzothiophene-2-carboxylic acid (CAS: 88791-07-5) typically synthesized?

7-Methoxy-1-benzothiophene-2-carboxylic acid is typically synthesized by reactin...

88791-07-57-methoxy-1-benzothi...

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 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.