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

文献信息

发布日期 2021-11-24
DOI 10.1039/D1RE00347J
影响因子 4.239
作者

Nuttapan Promsampao, Nuwong Chollacoop, Adisak Pattiya


查看原文

摘要

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.

相关文献

Synthesis, chiroptical properties and absolute configuration of spiro[1,3-benzodioxole-methanocyclooct[b]indole]

Eugenius Butkus, Julė Malinauskienė, Sigitas Stončius

2002-12-09 Paper

DOI: 10.1039/B208422H

Synthesis of CID-cleavable protein crosslinking agents containing quaternary amines for structural mass spectrometry

Susan E. Hagen, Kun Liu, Yafei Jin, Lolita Piersimoni, Hollis D. Showalter

2018-03-07 Communication

DOI: 10.1039/C8OB00329G

A pendant peptide endows a sunscreen with water-resistance

Aubrey J. Ellison

2018-09-10 Communication

DOI: 10.1039/C8OB01773E

l-Dopa and dopamine conjugated naphthalenediimides modulate amyloid β toxicity

Madhu Ramesh, Pandeeswar Makam, Chandrashekhar Voshavar, Harshavardhan Khare, Kolla Rajasekhar, Suryanarayanarao Ramakumar, Thimmaiah Govindaraju

2018-09-28 Paper

DOI: 10.1039/C8OB01691G

Synthesis of 2-trifluoromethylquinolines through rhodium-catalysed redox-neutral [3 + 3] annulation between anilines and CF3-ynones using traceless directing groups

Haichao Huang, Hailong Wang, Chao Gong, Zhenjing Zhuang, Wenmin Feng, Si-Hai Wu, Lianhui Wang

2021-11-29 Research Article

DOI: 10.1039/D1QO01478A

Dual function of amino acid ionic liquids (Bmim[AA]) on the degradation of the organophosphorus pesticide, Paraoxon®

Javiera I. Morales, Roberto Figueroa, Mabel Rojas, Daniela Millán, Ricardo A. Tapia, Paulina Pavez

2018-09-18 Paper

DOI: 10.1039/C8OB01928B

Contents list

Front/Back Matter

DOI: 10.1039/C8OB90138D

Iron-catalysed carbene-transfer reactions of diazo acetonitrile

Claire Empel, Katharina J. Hock, Rene M. Koenigs

2018-09-20 Communication

DOI: 10.1039/C8OB01991F

Inside front cover

Cover

DOI: 10.1039/C8OB90137F

您可能还喜欢

化合物问答

(5-氨基吡唑-3-基)乙酸(CAS号:174891-10-2)的物理化学性质是什么?

(5-氨基吡唑-3-基)乙酸是一种无色至白色固体,分子量为174.15 g/mol。它在水中具有较好的溶解性,在有机溶剂中的溶解度较低。该化合物具有较好的反应活...

174891-10-2(3-Amino-1H-pyrazol-...
化合物问答

3-氟-4,5-二氯苯胺(CAS号:35754-38-2)适用哪些法规指南?

3-氟-4,5-二氯苯胺受到多项法规指南的约束,包括但不限于GHS(全球化学品统一分类和标签制度)的危险分类标准、欧盟的REACH法规(注册、评估、授权和限制)...

35754-38-23,4-Dichloro-5-fluor...
化合物问答

什么是(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶(CAS号:442905-33-1)?

这是一种有机化合物,化学名为(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶,CAS号为44290...

442905-33-14,4'-Bis[bis(3,5-dim...
化合物问答

1-氨基-2-氰基萘(CAS号:3100-67-2)应用于哪些行业?

1-氨基-2-氰基萘在医药、聚合物、传感器和半导体等行业中有应用。在医药领域,它可用作中间体合成某些药物。在聚合物行业,它可以用于制备具有特定性能的聚合物。此外...

3100-67-21-Amino-2-naphthonit...
化合物问答

如何处理含有1-溴-4-(异丙氧基甲基)苯(CAS号:98446-84-5)的废料?

处理含1-溴-4-(异丙氧基甲基)苯的废料时,首先应确保废液收集在防渗漏的容器中,避免泄露。然后,可以考虑采用化学降解法或物理吸附法进行处理。在特定条件下,可通...

98446-84-51-Bromo-4-(isopropox...
化合物问答

6-Chloro-8-(trifluoromethyl)chroman-4-one(CAS号:1344889-75-3)的主要用途是什么?

6-氯-8-三氟甲基-2,3-二氢-4H-色喃-4-酮主要用于有机合成中的中间体,也可作为研究试剂使用。

1344889-75-36-Chloro-8-(trifluor...
化合物问答

7-乙氧基-2-萘酚(CAS号:57944-44-2)通常如何合成?

7-乙氧基-2-萘酚通常通过N-乙氧基化反应合成,首先将2-萘酚与乙醇钠在乙醇中反应生成7-乙氧基-2-萘酚钠盐,再通过酸化进一步得到7-乙氧基-2-萘酚。该合...

57944-44-27-Ethoxy-2-naphthol
化合物问答

4-(1,1-二氧硫代吗啉)丁醇(CAS号:59801-41-1)适用哪些法规指南?

该化合物需遵循一系列的法规指南,包括但不限于GHS全球统一分类和标签制度,其分类可能包括易燃液体和可能危害水生环境。在欧洲,还需遵循REACH法规,确保物质和混...

59801-41-14-(4-Hydroxybutyl)th...
化合物问答

4-甲氧基苄基叠氮甲酸酯(CAS号:25474-85-5)的物理化学性质是什么?

4-甲氧基苄基叠氮甲酸酯是一种无色液体,具有一定的挥发性。其分子量为198.16,熔点为-69°C,沸点为105°C。该化合物在水中溶解度较低,在有机溶剂如乙醇...

25474-85-54-Methoxybenzyl carb...
化合物问答

如何处理含有4-氯-2-氟嘧啶(CAS号:51422-00-5)的废料?

含有4-氯-2-氟嘧啶的废料应按照危险废物处理。首先,应收集并分类这些废料,避免与其他废物混合。然后,可以采用焚烧处理或者交由专业机构进行处置。在处理过程中,需...

51422-00-54-Chloro-2-fluoropyr...

来源期刊

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
自引率: 8.8%
年发文量: 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.

推荐供应商

免责声明
本页面提供的学术期刊信息仅供参考和研究使用。我们与任何期刊出版商均无关联,也不处理投稿事宜。如有投稿相关咨询,请直接联系相关期刊出版商。
如发现页面信息有误,请发送邮件至 support@chemtradehub.com 联系我们。我们将及时核实并处理您的问题。