Catalytic sugarcane bagasse transformation into a suitable biocrude for hydrocarbon production in typical refinery processes

Literature Information

Publication Date 2020-05-26
DOI 10.1039/D0SE00220H
Impact Factor 6.367
Authors

Débora N. dos Santos, Igor V. Pedrosa, Abdou Lachgar, Marcio Neli, Rafael Garrett, Yiu Lau Lam, Marcelo M. Pereira


View Original

Abstract

The conversion of biomass to green hydrocarbons offers great advantages to shorten our path to sustainability. Unfortunately, none of the existing approaches produces a biocrude that is compatible (in terms of density, viscosity, and reactivity) with current refinery processes. In this work, sugarcane bagasse was converted completely to a biocrude rich in O-isopropylidene acetals by an acetalization process using a continuous flow reactor. Hemicellulose is the first component that transformed into acetals followed by amorphous and crystalline cellulose. Hence, the composition of the biocrude to be collected under specific reaction conditions could be tuned in terms of the type of carbohydrate (pentoses and hexoses) and their derivatives. The process was also applied at a larger scale (20-fold increase) to produce a stable biocrude with density ≈1.2 g cm−3, viscosity of 200 cp (60 °C) and specific heat 1.8 J g °C−1 confirming its properties for conversion in typical refinery processes.

Related Literature

The base-catalysed cyclisation of phenyl N-(2-hydroxybenzyl)-N-methylcarbamates is concerted

Vojeslav Štěrba, Oldřich Hrabík, Jaromír Kaválek, Jaromír Mindl, Andrew Williams

2002-12-11 Paper

DOI: 10.1039/B209323P

Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum

Yi Guo, Na Zhang, Weiguang Sun, Xueyan Duan, Qing Zhang, Qun Zhou, Chunmei Chen, Hucheng Zhu, Zengwei Luo, Junjun Liu, Xiao-Nian Li, Yongbo Xue, Yonghui Zhang

2018-10-08 Paper

DOI: 10.1039/C8OB02067A

A donor–acceptor substituted molecular motor: unidirectional rotation driven by visible light

Richard A. van Delden, Nagatoshi Koumura, Annemarie Schoevaars, Auke Meetsma, Ben L. Feringa

2002-11-08 Communication

DOI: 10.1039/B209378B

A facile tandem decyanation/cyanation reaction of α-iminonitriles toward cyano-substituted amides

Pei Liang, Botao Liu, Haiqing Luo, Jing Zheng, Xiaowei Wen, Tanggao Liu, Min Ye

2018-10-25 Communication

DOI: 10.1039/C8OB02186D

DNA recognition by the anthracycline antibiotic respinomycin D: NMR structure of the intercalation complex with d(AGACGTCT)2

Mark S. Searle, Allister J. Maynard, Huw E. L. Williams

2002-12-05 Paper

DOI: 10.1039/B208622K

Intramolecular charge transfer with N-benzoylaminonaphthalenes. 1-Aminonaphthaleneversus2-aminonaphthalene as electron donors

Xuan Zhang, Chun-Hua Liu, Li-Hong Liu, Lin Guo, Chao-Jie Wang, Yun-Bao Jiang

2003-01-29 Paper

DOI: 10.1039/B210106H

Tuning the keto equilibrium in 4-substituted dipicolinic acid derivatives

Anne-Sophie Chauvin, Sandrine Gras, Jean-Claude G. Bünzli

2003-01-22 Paper

DOI: 10.1039/B211267C

Palladium-catalyzed cascade carboesterification of norbornene with alkynes

Can Li, Jianxiao Li, Huanfeng Jiang

2018-08-29 Paper

DOI: 10.1039/C8OB01799A

HIV-1 protease: mechanism and drug discovery

Ashraf Brik, Chi-Huey Wong

2002-11-26 Perspective

DOI: 10.1039/B208248A

Inherently chiral cone-calix[4]arenes via a subsequent upper rim ring-closing/opening methodology

José Augusto Berrocal, Matthew B. Baker, Laura Baldini, Alessandro Casnati, Stefano Di Stefano

2018-09-22 Paper

DOI: 10.1039/C8OB01813H

You might also like

Compound Q&A

Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?

4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...

84761-04-64-Benzyl-2,2-dimethy...
Compound Q&A

What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?

(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...

1346526-61-1(5,6-Dimethoxy-3-pyr...
Compound Q&A

How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?

1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...

67875-55-21,1,3,3-Tetramethyl-...
Compound Q&A

What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?

(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...

1018818-04-6(2R,4S)-1-Boc-4-meth...
Compound Q&A

What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?

When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...

22410-58-82,3-Dichloroacryloni...
Compound Q&A

How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?

(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...

1332832-16-2(S)-1-(o-Tolyl)ethan...
Compound Q&A

What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?

Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...

518047-98-8Benzyl [1-(hydroxyam...
Compound Q&A

What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?

2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...

885273-42-72-Methyloxazole-5-ca...
Compound Q&A

What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?

The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...

389889-82-12-Methyl-2-propanyl ...
Compound Q&A

Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?

1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...

26576-85-21-Butyl-3-methylpyri...
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.