Tetrahydrofuran-based two-step solvent liquefaction process for production of lignocellulosic sugars
文献情報
Arpa Ghosh, Martin R. Haverly, Jake K. Lindstrom, Patrick A. Johnston
Large-scale production of biofuels and chemicals will require cost-effective, sustainable, and rapid deconstruction of woody biomass into its constituent sugars. Here, we introduce a novel two-step liquefaction process for producing fermentable sugars from red oak using a mixture of tetrahydrofuran (THF), water and dilute sulfuric acid. THF promotes acid-catalyzed solubilization of lignin and hemicellulose in biomass achieving 61% lignin extraction and 64% xylose recovery in a mild pretreatment step. The pretreatment opens the structure of biomass through delignification and produces a cellulose-rich biomass, which is readily solubilized at low temperature giving 65% total sugar yields in a subsequent liquefaction process employing the same solvent mixture. This process achieves competitive sugar yields at high volumetric productivity compared to conventional saccharification methods. THF, which can be derived from renewable resources, has several benefits as solvent including ease of recovery from the sugar solution and relatively low toxicity and cost.
関連文献
Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Amelia García Fraile, David G. Morris, Antonio García Martínez, Santiago de la Moya Cerero, Kenneth W. Muir, Karl S. Ryder, Enrique Teso Vilar
DOI: 10.1039/B209427D
From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties
DOI: 10.1039/D0QO00723D
Stereoselective synthesis and applications of spirocyclic oxindoles
Alexander J. Boddy, James A. Bull
DOI: 10.1039/D0QO01085E
Trimeric and dimeric sesquiterpenoids from Artemisia atrovirens and their cytotoxicities
Tian-Ze Li, Chang-An Geng, Yun-Bao Ma, Xiao-Yan Huang, Jin-Ping Wang, Xue-Mei Zhang
DOI: 10.1039/D0QO01615B
An electrochemical perspective on the roles of ligands in the merger of transition-metal catalysis and electrochemistry
Jun-Song Zhong, Yi Yu, Zhaojiang Shi, Ke-Yin Ye
DOI: 10.1039/D0QO01227K
Recent advances in quinazolinones as an emerging molecular platform for luminescent materials and bioimaging
Zhiming Xing, Wanhui Wu, Yongxiang Miao, Yingqun Tang, Youkang Zhou, Lifang Zheng, Yang Fu, Zhibin Song, Yiyuan Peng
DOI: 10.1039/D0QO01425G
Rhodium-catalyzed annulation of pyrrole substituted BODIPYs with alkynes to access π-extended polycyclic heteroaromatic molecules and NIR absorption
Bixiang Zhou, Mengjie Guo, Qingjie Pan, Mingbo Zhou, Ling Xu, Yutao Rao, Kaisheng Wang, Bangshao Yin, Jie Zhou, Jianxin Song
DOI: 10.1039/D0QO01625J
Direct determination of rate constants for coupling between aromatic radical anions and alkyl and benzyl radicals by laser-flash photolysis
Torben Lund, Peter Christensen, Robert Wilbrandt
DOI: 10.1039/B209594G
こちらもおすすめ
1-{3-[5-(エチルカルボンイル)-2,4-ジメチル-1H-ピロロール-3-基]プロパニル}ピペリジン-4-カルボン酸について、適用される法規ガイドラインは何ですか?
この化合物はCAS番号1142209-81-1であり、GHS分類では corrosive (腐食性物質) と classified (分類物質) として指定され...
2,2-二氟-1,3-ベンゾジオキサン-5-カルボキシlic酸とは何ですか?
2,2-二氟-1,3-ベンゾジオキサン-5-カルボキシlic酸は、CAS番号656-46-2の化合物で、化学式はC8H4F2O4です。この化合物は白色の結晶性粉...
8-氯-4-色原酮の代替品はありますか?
8-氯-4-色原酮(CAS番号: 49701-11-3)の代替品には、他の色原酮類似物や、構造が似ている化合物があります。例えば、8-メチル-4-色原酮や、他の...
エチル6,6-ジメチル-4,5,6,7-テトラヒドロ-1H-インドアゼー-3-カルボキシレートとは何ですか?
エチル6,6-ジメチル-4,5,6,7-テトラヒドロ-1H-インドアゼー-3-カルボキシレートは、CAS番号1233243-56-5を有する化合物です。これは有...
4-叔丁基-6-氯-嘧啶に適用される法規ガイドラインは何ですか?
4-叔丁基-6-氯-嘧啶はCAS番号3435-24-3で、GHS分類では毒性物質とみなし、GHSの危険性分類が適用されます。REACH規則では登録が必要で、Eu...
維库溴铵杂质Bはどのように合成されますか?
維库溴铵杂质Bは、アンドロステンデンから始まり、一連の合成反応、包括的な選択性と高い収率で合成されます。具体的には、ブロミド化、酸化、ジマーゼ反応、アミド化など...
2-(4-氟苄基)-吡咯烷の物理化学的性質は何ですか?
CAS番号350017-04-8の2-(4-氟苄基)-吡咯烷は、結晶性の白色粉末です。分子量は199.17 g/molで、水に溶けにくいです。化学反応では比較的...
3-喹啉甲醛(2-チロール-8-エチル)は安全ですか?
3-喹啉甲醛(2-チロール-8-エチル)は一定の毒性を持つため、取扱には注意が必要です。使用する際は適切な防護具を着用し、密閉容器で保管・搬送し、直接的な接触を...
エチル3-(ヒドロキシメチル)-1H-ピロール-2-カルボキシレートはどのように保存すればよいですか?
エチル3-(ヒドロキシメチル)-1H-ピロール-2-カルボキシレートは、室温(25℃)以下で保存し、直射日光を避け、乾燥した環境で保管することが推奨されます。ま...
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.










![Ethyl (3aS,6aS)-1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate structure Ethyl (3aS,6aS)-1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate structure](https://static.chemtradehub.com/structs/894/894853-99-7-e175.webp)
![4-Chloro-1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridine structure 4-Chloro-1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridine structure](https://static.chemtradehub.com/structs/348/348640-05-1-7db8.webp)

![(S,S)-2-{1-Carboxy-2-[3-(3,5-dichloro-benzyl)-3H-imidazol-4-YL]-ethylamino}-4-methyl-pentanoic acid structure (S,S)-2-{1-Carboxy-2-[3-(3,5-dichloro-benzyl)-3H-imidazol-4-YL]-ethylamino}-4-methyl-pentanoic acid structure](https://static.chemtradehub.com/structs/305/305335-31-3-1724.webp)
