Regeneration of pristine HZSM-5 extrudates during the production of deeply deoxygenated bio-oil from ex situ catalytic fast pyrolysis of biomass in a bench-scale fluidised-bed reactor

Literature Information

Publication Date 2021-11-24
DOI 10.1039/D1RE00347J
Impact Factor 4.239
Authors

Nuttapan Promsampao, Nuwong Chollacoop, Adisak Pattiya


View Original

Abstract

Ex situ catalytic fast pyrolysis (ex-CFP) of biomass applying ZSM-5 catalysts is an effective method for deoxygenating the pyrolysis vapour, thus producing low-oxygen bio-oil in a single step. The catalysts deactivate after reactions but can be regenerated to recover their performance. Most of the previous studies on catalyst regeneration applied modified ZSM-5 catalysts to produce partially deoxygenated bio-oil with an oxygen content of around 10–25 wt%. In the deep deoxygenation region with bio-oil oxygen content below 5 wt%, the regeneration of pristine HZSM-5 catalyst used in ex-CFP where filtered pyrolysis vapour is upgraded has not been elucidated. Therefore, it is the main purpose of the current study to demonstrate the deep-deoxygenation capability of an unmodified HZSM-5 catalyst that has been previously depreciated. In this work, eucalyptus wood was pyrolysed in a bench-scale bubbling fluidised-bed reactor close-coupled with a separate catalytic reactor containing a fixed bed of pristine HZSM-5 extrudates. The produced catalytic bio-oil appears in 3 phases: light bio-oil, medium aqueous phase and heavy bio-oil. The light bio-oil has a very low oxygen content of ∼1 wt%, containing mainly monocyclic aromatic hydrocarbons, especially benzene, toluene and xylene. The heavy liquid had an oxygen content of 5–8 wt%, containing mainly naphthalene derivatives. The average degree of deoxygenation achieved in this work was 91% throughout the 10 experiments using fresh and regenerated catalysts. The unmodified HZSM-5 extrudates can be considered regenerable for up to 9 cycles with minor catalyst deactivation. The yields of main products including total bio-oil, char and gas were unaffected by the catalyst regeneration. However, the yield of light bio-oil appeared to gradually decrease with regeneration cycles. The regenerated catalyst could retain its surface area, morphology and structural framework to a great extent, albeit with small changes occurring on the surface area and volume of the micropores as well as its crystallinity and crystalline size.

Related Literature

Ni(ii)-Catalyzed intermolecular selective Heck-type arylation of unactivated alkenes with arylboronic acids

Cong Lin, Sai Chen, Yihua Wang, Fei Gao, Liang Shen

2021-12-01 Research Article

DOI: 10.1039/D1QO01579F

Aminative Umpolung cyclization for synthesis of chiral exocyclic vicinal diamines

Feng Liu, Guoqing Zhao, Weiqi Cai, Dongfang Xu, Baoguo Zhao

2018-09-26 Paper

DOI: 10.1039/C8OB02000K

Functionalization of diazotetronic acid and application in a stereoselective modular synthesis of pulvinone, aspulvinones A–E, G, Q and their analogues

Amarender Manchoju, Ritesh A. Annadate, Lise Desquien, Sunil V. Pansare

2018-08-10 Paper

DOI: 10.1039/C8OB01511B

Dependence of selective enclathration on types of cholic acid crystals

Nungruethai Yoswathananont, Kazuki Sada, Mikiji Miyata, Shigendo Akita, Kazunori Nakano

2002-11-29 Paper

DOI: 10.1039/B210544F

A stereodivergent, two-directional synthesis of stereoisomeric C-linked disaccharide mimetics

Michael Harding, Robert Hodgson, Tahir Majid, Kenneth J. McDowall

2002-12-17 Paper

DOI: 10.1039/B208781B

From α-keto acids to nitrile oxides enabled by copper nitrate: a facile access to fused isoxazolines

Yuping Zhu, Tianqi Liu, Bingxin Liu, Houguang Shi, Qitao Tan

2021-12-10 Research Article

DOI: 10.1039/D1QO01574E

Reactions of 5-mercaptoazoles and pyridine-2-thiones with acetylenic esters. Selectivity of the formation of novel fused thiazin-4-ones and thiazolidin-4-ones

Vasiliy A. Bakulev, Vera S. Berseneva, Natalia P. Belskaia, Yury Yu. Morzherin, Andreiy Zaitsev, Wim Dehaen, Ingrid Luyten, Suzanne Toppet

2002-12-05 Paper

DOI: 10.1039/B207854F

Back cover

Cover

DOI: 10.1039/C8OB90135J

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

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.