Nitrogen-doped carbon dots in transesterification reactions for biodiesel synthesis

Literature Information

Publication Date 2023-09-22
DOI 10.1039/D3LF00060E
Impact Factor 0
Authors

João P. de Mesquita


View Original

Abstract

Biodiesel has emerged as a sustainable renewable energy option and a promising substitute for traditional fossil fuel-derived petroleum. However, its current industrial production is financially impractical requiring novel approaches to ensure sustainability and commercial viability. Carbon dots (CDs) have recently been reported as promising heterogeneous catalysts for transesterification of oil to biodiesel yet the role of the surface chemistry remains vaguely understood. Here, we present amine-passivated CDs (N-CDs) as a model in which their surface chemistry, namely the degree of carboxylic acid to amine and amide functionalization, can be controlled by modifying the amine passivating agent. We thoroughly investigated the N-CDs physico-chemical properties and applied them as heterogeneous catalysts to transesterify canola oil to biodiesel. We report biodiesel conversions of ≥97% using 1 wt% catalyst loading at 100 °C for 3 hours even when the catalyst is reused for five reaction cycles. Lastly, we investigate the effects of modifying the carbon dot surface groups and postulate a plausible governing mechanism for the N-CD-catalyzed transesterification of canola oil to biodiesel. Our findings suggest that both carboxylic acids and amines can act as active catalytic sites, and depending on their concentration, two different reaction mechanisms are possible.

Related Literature

Facile protocol for the highly regioselective and stereodivergent synthesis of substituted bishomoallylic alcohols from esters

Martin Oestreich, Fernando Sempere-Culler

2004-02-17 Communication

DOI: 10.1039/B315758J

Palladium catalysed cyclisation–carbonylation of enynes to give cyclic γ,δ-unsaturated acids

Varinder K. Aggarwal, Mike Butters, Paul W. Davies

2003-04-02 Communication

DOI: 10.1039/B300719G

Formation of dimers of inclusion cryptand/paraquat complexes driven by dipole–dipole and face-to-face π-stacking interactions

Feihe Huang, Liang Zhou, Jason W. Jones, Harry W. Gibson, Mehdi Ashraf-Khorassani

2004-10-14 Communication

DOI: 10.1039/B411234B

Ensemble hybridisation – a new method for exploring sequence dependent fluorescence of dye–nucleic acid conjugates

Olaf Köhler, Dilip Venkatrao Jarikote, Oliver Seitz

2004-10-14 Communication

DOI: 10.1039/B411877D

Monitoring the formation of biosilica catalysed by histidine-tagged silicatein

Muhammad Nawaz Tahir, Patrick Théato, Werner E. G. Müller, Heinz C. Schröder, Andreas Janshoff, Jian Zhang, Joachim Huth, Wolfgang Tremel

2004-10-27 Communication

DOI: 10.1039/B410283E

Selective growth of a less stable polymorph of 2-iodo-4-nitroaniline on a self-assembled monolayer template

Rupa Hiremath, Stephen W. Varney, Jennifer A. Swift

2004-10-15 Communication

DOI: 10.1039/B411649F

Attachment of glycosaminoglycan oligosaccharides to thiol-derivatised gold surfaces

Susannah J. Patey, Jeremy E. Turnbull

2004-10-11 Communication

DOI: 10.1039/B411726C

Dispersing palladium nanoparticles using a water-in-oil microemulsion—homogenization of heterogeneous catalysis

Byunghoon Yoon, Hakwon Kim, Chien M. Wai

2003-04-02 Communication

DOI: 10.1039/B211836J

Cyclopropyl fatty acids implicate a radical but not a cation as an intermediate in P450BM3-catalysed hydroxylations

Max J. Cryle, Julia M. U. Stuthe, Paul R. Ortiz de Montellano, James J. De Voss

2004-01-27 Communication

DOI: 10.1039/B315911F

You might also like

Compound Q&A

What industries use (1R,3S)-1,3-Cyclopentanediol (CAS: 16326-97-9)?

(1R,3S)-1,3-Cyclopentanediol finds applications in various industries. In the ph...

16326-97-9(1R,3S)-1,3-Cyclopen...
Compound Q&A

What precautions should be taken when handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine (CAS: 637-31-0)?

When handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine, it i...

637-31-0N'-[4-(Dimethylamino...
Compound Q&A

Are there alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine (CAS: 1352318-16-1) in synthesis?

There are several alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine in ...

1352318-16-15-(2,4-Difluoropheny...
Compound Q&A

What regulatory guidelines apply to 1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6)?

1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6) must comply with the Globally...

382141-68-61-(3-Methoxyphenoxy)...
Compound Q&A

Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?

Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...

18660-81-6Tetrodotoxin Citrate
Compound Q&A

What are the main uses of 2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9)?

2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9) i...

225641-84-92-Methyl-2-propanyl ...
Compound Q&A

How should waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) be handled?

Waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) ...

16261-80-64-(2-Hydroxyhexafluo...
Compound Q&A

How is 2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl}carbamate (CAS: 102507-19-7) typically synthesized?

2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl...

102507-19-72-Methyl-2-propanyl ...
Compound Q&A

What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?

Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...

20735-15-3Benzeneethanamine, α...
Compound Q&A

Are there alternatives to 3-{(E)-[4-(Dimethylamino)phenyl]diazenyl}benzoic acid (CAS: 20691-84-3) in synthesis?

In the synthesis of compounds similar to 3-{(E)-[4-(Dimethylamino)phenyl]diazeny...

20691-84-33-{(E)-[4-(Dimethyla...
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.