α-Oxidation of banana lignin with atmospheric oxygen catalyzed by Co3O4
文献情報
Carlos Augusto Cabral Kramer, Luciene Santos de Carvalho
Lignin is an important macromolecule present in biomass, and its structure contains a great diversity of aromatic rings and organic chains that can potentially be converted into smaller molecules with high added value. Several methods for the derivatization of lignin are considered in the literature; however, they come up against the high recalcitrance of lignin. As an alternative, oxidation of α-hydroxyls, as a preliminary step, facilitates the breakdown of its polymeric chain. An efficient oxidative method was developed in this work, consisting of the oxidation of banana organosolv lignin via atmospheric oxygen gas in the presence of Co3O4 as a heterogeneous catalyst at a temperature of 80 °C and ambient pressure. The ideal concentration of the catalyst is 1% (mol/mol), which after 54 hours of reaction was sufficient for the maximum growth of the intensity of the carbonyl band at 1710 cm−1 (by FTIR), increasing the transmittance by 0.32%. A decrease in intensity by 0.31% of the band at 3400–3430 cm−1 is also observed (hydroxyls), confirming the effectiveness of the method and the conversion capacity of the catalyst. The non-appearance/intensification of other bands is attributed to the good selectivity of Co3O4.
関連文献
Vibrationally promoted electron emission at a metal surface: electron kinetic energy distributions
Jerry LaRue, Tim Schäfer, Daniel Matsiev, Luis Velarde, N. Hendrik Nahler, Daniel J. Auerbach
DOI: 10.1039/C0CP01626H
Folding oligomers of difluorinated thienylfurans: a DFT study
DOI: 10.1039/B916415D
An ab initio insight into the Cu(111)-mediated Ullmann reaction
Manh-Thuong Nguyen, Carlo A. Pignedoli, Daniele Passerone
DOI: 10.1039/C0CP00759E
Solvent polarity effect on intramolecular electron transfer in a corrole–naphthalene bisimide dyad
Lucia Flamigni, Dagmara Wyrostek, Roman Voloshchuk, Daniel T. Gryko
DOI: 10.1039/B916525H
The interaction of H2O2 with ice surfaces between 203 and 233 K
N. Pouvesle, M. Kippenberger, G. Schuster, J. N. Crowley
DOI: 10.1039/C0CP01656J
NMR study on relationships between reorientational dynamics and phase behaviour of room-temperature ionic liquids: 1-alkyl-3-methylimidazolium cations
Mamoru Imanari, Kei-ichi Uchida, Kozue Miyano, Hiroko Seki, Keiko Nishikawa
DOI: 10.1039/B922931K
ZnO-based dye solar cell with pure ionic-liquid electrolyte and organic sensitizer: the relevance of the dye–oxide interaction in an ionic-liquid medium
E. Guillén, J. Idígoras, T. Berger, J. A. Anta, C. Fernández-Lorenzo, R. Alcántara, J. Navas, J. Martín-Calleja
DOI: 10.1039/C0CP00507J
The zone-refine driven growth of jellyfish-like core–shell nanowires
Jyun-Lin Wu, Hsin-Fu Kuo, Ping-Tzu Chen, Hung-Jen Chen, Su-Jien Lin, Wen-Kuang Hsu
DOI: 10.1039/C0CP00890G
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Reaction Chemistry & Engineering

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.














