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Dramatic Simplification of Lignin Heteronuclear Single Quantum Coherence Spectra from Ring-and-Puck Milling Followed by Oxidation

机译:环糊精制粉和氧化后木质素异核单量子相干谱的显着简化

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摘要

Conversion of biomass into usable fuels and chemicals, especially under very low-cost processing, remains a major challenge. Mechanochemical treatment of lignin can greatly improve the yield of monomer products that can be obtained by oxidative deconstruction. In this study, we applied a mechanochemical approach using ring-and-puck milling with KOH in a solvent-free system to promote lignin degradation. We investigated how milling with this larger scale method would affect the success of a two-step oxidative lignin deconstruction strategy, in which we previously employed small-scale ball milling. We monitored changes in the lignin structure and functionality using heteronuclear single quantum coherence (HSQC) and P-31 nuclear magnetic resonance (NMR) spectroscopy. P-31 NMR indicated that 2 h of ring-and-puck milling can generate significant amounts of aliphatic hydroxyls and phenols. Dramatic simplification of the HSQC spectra and a pronounced downfield shift in NMR resonances (to delta(H) 8.5 and 8.8 ppm) after porphyrin oxidation suggests that ring-and-puck milling produced a significantly different set of reactions and products than is produced by the ball-milling technique that we used in a previous study. Also, in contrast to our findings with ball-milled material, porphyrin oxidation of the ring-and-puck milled material produced new products that could not be reduced with NaBH4 to reform the starting material. In addition, Baeyer Villiger oxidation produced a remarkable increase in the amount of the ethyl-acetate-soluble portion as well as a decrease in the insoluble solid compared to the amounts obtained from the ball-milling process. A short 2 h period of ring-and-puck milling produced nearly half of the amount of vanillic acid (isolated as the methyl ester) as was previously isolated after an extended (48 h) period of ball milling. The significant changes in the HSQC spectrum, the irreversibility of the oxidation step, and the dramatic increase in ethyl-acetate-soluble products suggest that previously unobserved chemistry is taking place.
机译:将生物质转化为可用的燃料和化学品,尤其是在非常低成本的处理下,仍然是一个重大挑战。木质素的机械化学处理可以大大提高可通过氧化解构得到的单体产物的产率。在这项研究中,我们采用了机械化学方法,在无溶剂的系统中使用KOH进行环鼓和圆盘磨,以促进木质素降解。我们研究了用这种较大规模的方法进行研磨将如何影响两步氧化木质素解构策略的成功,该策略以前采用了小规模的球磨。我们使用异核单量子相干(HSQC)和P-31核磁共振(NMR)光谱监测了木质素结构和功能的变化。 P-31 NMR表明,圆盘和圆盘研磨2小时可以产生大量的脂肪族羟基和酚。卟啉氧化后,HSQC光谱得到显着简化,NMR共振明显下移(至δ(H)8.5和8.8 ppm),这表明环和冰球磨制得的反应和产物与苯丙氨酸的产生显着不同。我们在先前的研究中使用的球磨技术。此外,与我们对球磨材料的发现相反,环和球磨材料的卟啉氧化产生了新产品,而NaBH4不能还原该新产品以重整原材料。另外,与通过球磨法获得的量相比,Baeyer Villiger氧化显着增加了乙酸乙酯可溶部分的量,并且减少了不溶固体的量。在延长的球磨时间(48 h)之后,之前进行的短短的2 h环球磨制生产了将近一半的香草酸(分离为甲酯)。 HSQC谱图中的显着变化,氧化步骤的不可逆性以及可溶于乙酸乙酯的产物的急剧增加表明发生了以前无法观察到的化学反应。

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  • 来源
    《Energy & fuels》 |2018年第11期|11632-11638|共7页
  • 作者单位

    Univ Kentucky, Dept Chem, Lexington, KY 40506 USA;

    Univ Kentucky, Dept Chem, Lexington, KY 40506 USA;

    Univ Kentucky, Dept Chem, Lexington, KY 40506 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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