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首页> 外文期刊>Journal of Cleaner Production >Valorization of biomass from plant microbial fuel cells into levulinic acid by using liquid/solid acids and green solvents
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Valorization of biomass from plant microbial fuel cells into levulinic acid by using liquid/solid acids and green solvents

机译:采用液体/固酸和绿色溶剂将生物量从植物微生物燃料电池中的储度到乙酰丙酸中

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摘要

Plant microbial fuel cells are attractive for treating hexavalent chromium contaminated soils while generating renewable electricity. The end-of-service-life plant microbial fuel cells, however, may pose a risk to secondary pollution. In this study, we propose a novel valorization of Chinese pennisetum plant microbial fuel cell waste into levulinic acid using liquid or solid acid catalyst in green solvents, water and/or gamma-valerolactone, under microwave heating. The results showed that the use of 1 M sulfuric acid at 150 degrees C in 60 min can obtain approximately 15.2 C mol% of levulinic acid. In view of the use of gamma-valerolactone, the addition of H2O showed beneficial effects to improve levulinic acid yield by facilitating cellulose hydration and sugar dehydration-rehydration reactions, for instance, levulinic acid yield increased to 20 C mol% when gamma-valerolactone to water ratio changed from 100/0 v/v to 70/30 v/v. The scanning electron microscope images proved that the cellulose structure was recalcitrant in H2O under the catalysis of Amberlyst 36, while the cellulose structure was altered under gamma-valerolactone to water regardless of the type of catalysts. The X-ray diffraction patterns provided spectroscopic evidence for the enhanced dissolution or hydrolysis of cellulose in a short period of time. The thermal stability of the solid residues after microwave heating at 180 degrees C was enhanced due to polymerization reaction. The C-13 solid-state Nuclear magnetic resonance spectra revealed that remaining gamma-valerolactone and polymerization byproducts were the major residues after the catalytic reaction under pure gamma-valerolactone or at high temperature. The measurement of total chromium and hexavalent chromium distribution confirmed that the metal pre-absorbed in plant biomass all remained in the solid phase, indicating the liquid phase was free of secondary pollution. The proposed valorization plan could innovatively utilize hazardous waste from plant microbial fuel cells to produce value-added chemicals in a sustainable way. (C) 2020 Elsevier Ltd. All rights reserved.
机译:植物微生物燃料电池对于治疗六价铬污染的土壤具有吸引力,同时产生可再生电力。然而,使用寿命植物微生物燃料细胞可能对二次污染构成风险。在这项研究中,我们在微波加热下,在绿色溶剂,水和/或γ-丙酮酮中,使用液体或固体酸催化剂在紫水酸中提出了紫杉醇的新载玻片。结果表明,在60分钟内使用1M硫酸在60分钟内可以获得约15.2℃的乙酰丙酸。鉴于使用γ-戊酮的使用,通过促进纤维素水合和糖脱水 - 再水化反应,增加H2O的加入效果,以改善乙酰丁酸产率,例如,当γ-戊酮时,乙酰丙酸产率增加到20℃摩尔%。水比从100/0 v / v到70/30 v / v变化。扫描电子显微镜图像证明纤维素结构在H2O下在催化剂36的催化下在H 2 O中克隆,而无论催化剂的类型如何,纤维素结构都会在γ-戊酰胺中改变为水。 X射线衍射图案提供了在短时间内增强纤维素的增强或水解的光谱探测。由于聚合反应,增强了在180℃下微波加热后固体残基的热稳定性。 C-13固态核磁共振谱显示,剩余的γ-戊酰胺和聚合副产物是在纯γ-戊内酯或高温下催化反应后的主要残基。总铬和六价铬分布的测量证实,在植物生物质中预先吸收的金属仍然存在于固相中,表明液相不含二次污染。拟议的价值计划可以创新地利用来自植物微生物燃料电池的危险废物,以可持续的方式生产增值化学品。 (c)2020 elestvier有限公司保留所有权利。

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