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在含有酸性离子液体的介质中由松木多糖制备平台化学品

Manufacture of Platform Chemicals from Pine Wood Polysaccharides in Media Containing Acidic Ionic Liquids.

作者信息

López Mar, Vila Carlos, Santos Valentín, Parajó Juan Carlos

机构信息

Chemical Engineering Department, University of Vigo (Campus Ourense), Polytechnical Building, As Lagoas, 32004 Ourense, Spain.

出版信息

Polymers (Basel). 2020 May 27;12(6):1215. doi: 10.3390/polym12061215.

Abstract

wood samples were subjected to chemical processing for manufacturing furans and organic acids from the polysaccharide fractions (cellulose and hemicellulose). The operation was performed in a single reaction stage at 180 or 190 °C, using a microwave reactor. The reaction media contained wood, water, methyl isobutyl ketone, and an acidic ionic liquid, which acted as a catalyst. In media catalyzed with 1-butyl-3-methylimidazolium hydrogen sulfate, up to 60.5% pentosan conversion into furfural was achieved, but the conversions of cellulose and (galacto) glucomannan in levulinic acid were low. Improved results were achieved when AILs bearing a sulfonated alkyl chain were employed as catalysts. In media containing 1-(3-sulfopropyl)-3-methylimidazolium hydrogen sulfate as a catalyst, near quantitative conversion of pentosans into furfural was achieved at a short reaction time (7.5 min), together with 32.8% conversion of hexosans into levulinic acid. Longer reaction times improved the production of organic acids, but resulted in some furfural consumption. A similar reaction pattern was observed in experiments using 1-(3-sulfobutyl)-3-methylimidazolium hydrogen sulfate as a catalyst.

摘要

木材样品经过化学处理,以从多糖组分(纤维素和半纤维素)制造呋喃和有机酸。该操作在180或190°C的单一反应阶段中,使用微波反应器进行。反应介质包含木材、水、甲基异丁基酮和一种酸性离子液体,该酸性离子液体用作催化剂。在用硫酸氢1-丁基-3-甲基咪唑鎓催化的介质中,戊聚糖转化为糠醛的转化率高达60.5%,但纤维素和(半乳)葡甘露聚糖转化为乙酰丙酸的转化率较低。当使用带有磺化烷基链的酸性离子液体作为催化剂时,可获得更好的结果。在含有硫酸氢1-(3-磺丙基)-3-甲基咪唑鎓作为催化剂的介质中,在较短的反应时间(7.5分钟)内实现了戊聚糖几乎定量转化为糠醛,同时己聚糖转化为乙酰丙酸的转化率为32.8%。更长的反应时间提高了有机酸的产量,但导致了一些糠醛的消耗。在使用硫酸氢1-(3-磺丁基)-3-甲基咪唑鎓作为催化剂的实验中观察到了类似的反应模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a253/7362180/0f7520620c7b/polymers-12-01215-g001.jpg

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