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

文献情報

出版日 2021-11-24
DOI 10.1039/D1RE00347J
インパクトファクター 4.239
著者

Nuttapan Promsampao, Nuwong Chollacoop, Adisak Pattiya


原文を見る

要旨

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.

関連文献

Cobalt promoted copper manganese oxide catalysts for ambient temperature carbon monoxide oxidation

Christopher Jones, Stuart H. Taylor, Andrew Burrows, Mandy J. Crudace, Christopher J. Kiely, Graham J. Hutchings

2008-02-01 Communication

DOI: 10.1039/B800052M

Front cover

Cover

DOI: 10.1039/B805043K

Interpenetrating single helical capsules

Emanuela Berni, Joachim Garric, Corinne Lamit, Brice Kauffmann, Jean-Michel Léger, Ivan Huc

2008-02-28 Communication

DOI: 10.1039/B719712H

Chromonic liquid crystals: properties and applications as functional materials

Suk-Wah Tam-Chang, Liming Huang

2008-01-07 Feature Article

DOI: 10.1039/B714319B

Contents and Chemical Technology

Front/Back Matter

DOI: 10.1039/B804231B

Photo-responsive gel droplet as a nano- or pico-litre container comprising a supramolecular hydrogel

Shinji Matsumoto, Satoshi Yamaguchi, Atsuhiko Wada, Toshihiro Matsui, Masato Ikeda

2008-02-25 Communication

DOI: 10.1039/B719004B

Angle-controlled arrangement of single-walled carbon nanotubes solubilised by 8-quinolinol metal chelate derivatives on mica

Kazuyuki Nobusawa, Atsushi Ikeda, Yasunori Tanaka, Mineo Hashizume, Jun-ichi Kikuchi, Michihiro Shirakawa, Tatsuya Kitahara, Norifumi Fujita, Seiji Shinkai

2008-02-26 Communication

DOI: 10.1039/B715960A

One-pot synthesis of reverse type-I In2O3@In2S3 core–shell nanoparticles

Zhaoyong Sun, Amar Kumbhar, Kai Sun, Qingsheng Liu

2008-03-18 Communication

DOI: 10.1039/B719176F

Synthesis and reactivity of tetrakis(imino)pyracene (TIP) ligands; bifunctional analogues of the BIAN ligand class

Kalyan V. Vasudevan, Michael Findlater, Alan H. Cowley

2008-03-03 Communication

DOI: 10.1039/B719251G

Functionalized polyesters from organocatalyzed ROP of gluOCA, the O-carboxyanhydride derived from glutamic acid

Olivier Thillaye du Boullay, Colin Bonduelle, Blanca Martin-Vaca, Didier Bourissou

2008-03-17 Communication

DOI: 10.1039/B800852C

こちらもおすすめ

化合物よくある質問

3-イチチルビフェニルはどのように合成されますか?

3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。

5668-93-93-Ethylbiphenyl
化合物よくある質問

8-溴-5-三氟甲基喹啉はどのように合成されますか?

8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...

917251-92-48-Bromo-5-(trifluoro...
化合物よくある質問

ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?

ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...

741709-66-0Dimethyl 4-(4,4,5,5-...
化合物よくある質問

N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?

N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...

199871-63-1N-(3,5-Dichloro-4-py...
化合物よくある質問

イソステアロイルグリセリルは安全ですか?

イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...

222723-55-92-[(5Z,8Z,11Z,14Z)-5...
化合物よくある質問

1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?

1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...

288315-02-61-Benzhydryl-3,3-dif...
化合物よくある質問

3-チオフェンスチオールの物理化学的性質は何ですか?

3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...

7774-73-43-Thiophenethiol
化合物よくある質問

2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?

2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...

475105-35-22-Methyl-2-propanyl ...
化合物よくある質問

CAS番号1316822-90-8の化合物は安全ですか?

CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...

1316822-90-8Gal beta(1-3)[Neu5Ac...
化合物よくある質問

Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?

Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。

517866-79-4Tert-butyl 2-(2-hydr...

掲載誌

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
自己引用率: 8.8%
年間論文数: 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.

おすすめサプライヤー

免責事項
このページに表示される学術雑誌情報は、参考および研究目的のみを目的としています。当社は雑誌出版社とは提携しておらず、投稿の取り扱いも行っておりません。出版に関するお問い合わせは、各雑誌出版社に直接ご連絡ください。
表示されている情報に誤りがある場合は、support@chemtradehub.com までご連絡ください。迅速に確認し、対応いたします。