Nitrogen-doped carbon dots in transesterification reactions for biodiesel synthesis
Literature Information
João P. de Mesquita
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
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
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
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
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
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
DOI: 10.1039/B411649F
Crystallography and magnetism of radicals with hindered hydroxyl groups: 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole-3-oxide-1-oxyl and 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole-1-oxyl
Patrick Taylor, Paul M. Lahti
DOI: 10.1039/B411574K
Attachment of glycosaminoglycan oligosaccharides to thiol-derivatised gold surfaces
Susannah J. Patey, Jeremy E. Turnbull
DOI: 10.1039/B411726C
Dispersing palladium nanoparticles using a water-in-oil microemulsion—homogenization of heterogeneous catalysis
Byunghoon Yoon, Hakwon Kim, Chien M. Wai
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
DOI: 10.1039/B315911F
You might also like
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...
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...
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 ...
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...
Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?
Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...
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...
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) ...
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...
What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?
Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...
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...















