Probing the effects of fructose concentration on the evolution of humins during fructose dehydration

Literature Information

Publication Date 2022-10-11
DOI 10.1039/D2RE00324D
Impact Factor 4.239
Authors

Yexin Hu, Hui Li, Ping Hu, Linzhen Li, Di Wu, Zhidan Xue, Liangfang Zhu, Changwei Hu


View Original

Abstract

5-Hydroxymethylfurfural (HMF), considered as a “sleeping giant” of sustainable chemistry, is generally produced by fructose dehydration. Till now, high HMF yields have been achieved, whereas large-scale production of HMF is hampered by the formation of undesired humins, especially at higher fructose concentrations (>10 wt%). In this work, we report the effects of fructose concentration (4.5–360.0 wt%) on the evolution pathways of humins during the H2SO4-catalyzed dehydration of fructose in water. We show that both etherification–dehydration–condensation and degradative condensation of fructose and/or HMF are involved in the formation of humins, wherein the increase of fructose concentration promotes the former path and inhibits the latter one because of the promotional effect on the formation of difructose anhydride (DFA) species. The progressive dehydrations and condensations of DFAs under experimental conditions lead to humins, but the reversible hydrolysis of DFAs to fructose favors the HMF formation. Further, we demonstrate that the addition of a typical polar aprotic solvent such as tetrahydrofuran (THF) or 1,4-dioxane (DIO) to water as a co-solvent could stabilize the DFA species and increase the HMF yield by more than 10% in the conversion of high-concentration fructose (72.0 wt%). This understanding provides an indispensable insight on factors influencing humin formation for future advances on HMF biorefineries.

Related Literature

Revealing the base pair stepping dynamics of nucleic acidmotorproteins with optical traps

Yann R. Chemla

2010-02-19 Perspective

DOI: 10.1039/B920234J

On the use and influence of electron-blocking interlayers in polymer light-emitting diodes

Peter A. Levermore, Jingsong Huang, Xuhua Wang, Donal D. C. Bradley

2009-03-06 Paper

DOI: 10.1039/B819200F

Combining density functional theory (DFT) and pair distribution function (PDF) analysis to solve the structure of metastable materials: the case of metakaolin

Claire E. White, John L. Provis, Thomas Proffen, Daniel P. Riley, Jannie S. J. van Deventer

2010-02-22 Paper

DOI: 10.1039/B922993K

Dipole effects on molecular and electronic structures in a novel conjugate of oligo(phenyleneethynylene) and helical peptide

Hidenori Nakayama, Tomoyuki Morita, Shunsaku Kimura

2009-03-10 Paper

DOI: 10.1039/B817685J

Bifunctional polyacrylamide based polymers for the specific binding of hexahistidine tagged proteins on gold surfaces

Lucas B. Thompson, Nathan H. Mack, Ralph G. Nuzzo

2009-12-04 Paper

DOI: 10.1039/B920713A

Inside front cover

Front/Back Matter

DOI: 10.1039/C003911J

Back matter

Front/Back Matter

DOI: 10.1039/C004807K

Synthesis and characterization of V2O3 nanorods

Alexander C. Santulli, Wenqian Xu, Liusuo Wu, Fen Zhang, Chang-Yong Nam, Charles T. Black, Amanda L. Tiano

2009-03-12 Paper

DOI: 10.1039/B822902C

Probing the hydrogen-bond network of watervia time-resolved soft X-ray spectroscopy

Nils Huse, Haidan Wen, Dennis Nordlund

2009-03-10 Paper

DOI: 10.1039/B822210J

You might also like

Compound Q&A

How should waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) be handled?

Waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) ...

88634-80-42-Ethyl-4-Methyl-1H-...
Compound Q&A

What industries use Triethoxy(octyl)silane (CAS: 1385031-14-0)?

Triethoxy(octyl)silane (CAS: 1385031-14-0) is widely used in the pharmaceuticals...

1385031-14-0Triethoxy(octyl)sila...
Compound Q&A

Are there alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) in synthesis?

Several alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) exist in t...

864724-64-13-iodo-7-nitro-1H-in...
Compound Q&A

Are there alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317-71-9) in synthesis?

Yes, there are alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317...

266317-71-9Benzene, bis[(trimet...
Compound Q&A

Is Isothiazole-3-carbonitrile (CAS: 1452-17-1) safe?

Isothiazole-3-carbonitrile (CAS: 1452-17-1) is generally considered safe when us...

1452-17-1Isothiazole-3-carbon...
Compound Q&A

Is (3-Chlorophenyl)methanol (CAS: 873-63-2) safe?

(3-Chlorophenyl)methanol (CAS: 873-63-2) is considered low to moderately toxic. ...

873-63-2(3-Chlorophenyl)meth...
Compound Q&A

How is (2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)propanoic acid (CAS: 959583-98-3) typically synthesized?

(2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)pr...

959583-98-3(2S,3S)-2-Hydroxy-3-...
Compound Q&A

What precautions should be taken when handling Methyl 2-(bromomethyl)-5-methoxybenzoate (CAS: 788081-99-2)?

Proper handling of methyl 2-(bromomethyl)-5-methoxybenzoate requires the use of ...

788081-99-2Methyl 2-(bromomethy...
Compound Q&A

What is 6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3)?

6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3) is an aro...

904805-36-36,8-Dibromoimidazo[1...
Compound Q&A

Is 3-Amino-5-bromo-2-pyridinecarbonitrile (CAS: 573675-27-1) safe?

3-Amino-5-bromo-2-pyridinecarbonitrile is considered safe when handled under pro...

573675-27-13-Amino-5-bromo-2-py...

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.