Detailed kinetics of substituted phenolic species in pyrolysis bio-oils
Literature Information
Matteo Pelucchi, Carlo Cavallotti, Alberto Cuoci, Tiziano Faravelli, Alessio Frassoldati, Eliseo Ranzi
Fast biomass pyrolysis is an effective and promising process to obtain high yields of bio-oils, whose upgrading provides valuable fuels for energy application or chemicals for industry. The growing interest in the use of bio-oils in combustion devices to produce energy motivates this study, in which we present the first comprehensive kinetic model to describe systematically the pyrolysis and combustion of substituted phenolic species, considered as reference components in bio-oil surrogate mixtures. In fact, bio-oils are complex liquid mixtures, containing a large variety of oxygenated organic species. Within these species, substituted phenolic compounds are one of the most significant fractions (∼20–30 wt%). A reliable characterization of the combustion properties and pollution potential of bio-oils strongly depends on the accurate knowledge of their combustion chemistry. While some experimental and kinetic modeling studies on pyrolysis and combustion of phenol, anisole, and catechol are available in the literature, only limited efforts have been devoted to the understanding of the decomposition and oxidation kinetics of guaiacol (2-methoxyphenol) and vanillin (4-hydroxy-3-methoxybenzaldehyde). Accurate theoretical calculations of bond dissociation energies have been performed to assess proximity effects originating from multiple substitutions on the aromatic ring. Based on these evaluations and on previous studies, rate rules and reference kinetic parameters are proposed for major pyrolysis and combustion reaction classes. Satisfactory comparisons of model predictions with experimental data of pyrolysis and combustion of anisole, catechol, guaiacol, and vanillin hierarchically support the development and the reliability of the proposed kinetic model. This work provides a valuable basis for further developments and strongly motivates additional experimental, theoretical, and kinetic modelling efforts in the area of reference components for bio-oil surrogates.
Related Literature
Homo- and copolymerization of norbornene using tridentate IzQO palladium catalysts with dimethylaminoethyl as a side arm‡
Jie Dong
DOI: 10.1039/D1PY00699A
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
DOI: 10.1039/B100610J
Dissociate transfer exchange of tandem dynamic bonds endows covalent adaptable networks with fast reprocessability and high performance
Songqi Ma, Zhen Yu, Jin Zhu
DOI: 10.1039/D1PY01045J
The dissociation kinetics of dissolved metal–humate complexes
Samantha J. King, Peter Warwick, Anthony Hall, Nicholas D. Bryan
DOI: 10.1039/B004899M
Molecular simulation of hydrogen adsorption in graphitic nanofibres
DOI: 10.1039/B100144M
Laser induced, dispersed fluorescence spectroscopy, and ab initio calculations of p-cyanophenol
Wolfgang Roth, Petra Imhof, Karl Kleinermanns
DOI: 10.1039/B100883H
Induction, fixation and recovery of self-organized helical superstructures in achiral liquid crystalline polymer
Tengfei Miao, Xiaoxiao Cheng, Haotian Ma, Wei Zhang, Xiulin Zhu
DOI: 10.1039/D1PY01206A
You might also like
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...
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...
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 ...
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...
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...
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 ...
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...
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...
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...
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...
Source Journal
Reaction Chemistry & Engineering

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.












![Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, compd. with 1-pyrrolidineethanol (1:1) structure Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, compd. with 1-pyrrolidineethanol (1:1) structure](https://static.chemtradehub.com/structs/119/119623-66-4-5301.webp)

