首页> 外文期刊>Energy & fuels >Depolymerization of Polyester Polymers from the Oxidation of Soybean Biodiesel
【24h】

Depolymerization of Polyester Polymers from the Oxidation of Soybean Biodiesel

机译:大豆生物柴油氧化对聚酯聚合物的解聚作用

获取原文
获取原文并翻译 | 示例
           

摘要

Aging of soybean biodiesel at an elevated temperature (90 degrees C) with aeration, simulating diesel engine fuel system conditions, yielded higher molecular weight materials and increased kinematic viscosity. A considerable proportion of the incorporated oxygen was identified as new ester bonds, beyond those in the biodiesel fatty acid methyl esters (FAMEs). The purpose of this study was to characterize the high molecular weight components of oxidized biodiesel fuel and understand the contribution of esters to the increased viscosity through experiments to depolymerize ester and ether bonds. Methods used to characterize high molecular weight materials included acid and base transesterification of oxidized biodiesel with methanol; hydrolysis with hydroiodic acid (HI); and GC-MS, gel permeation chromatography, FTIR, and C-13 NMR of the aged and transesterified materials. Depolymerization via transesterification with NaOCH3 or CH3OH/HCl, specifically targeting ester bonds, resulted in a marked reduction in the molecular weight distribution and viscosity of the aged biodiesel. Depolymerization with HI, targeting both ester and ether bonds, showed no additional reduction in molecular weight or kinematic viscosity, suggesting that ether bonds play a negligible role. FTIR spectra showed a shift in carbonyl stretching vibrations after depolymerization treatments consistent with ester involvement. With GC-MS, dicarboxylic acids were tentatively identified in the depolymerized products that were not present in the untreated aged biodiesel, suggesting a role as cross-linking agents in forming polyester products. Finally, C-13 NMR showed data consistent with biodiesel having undergone significant oxidation yielding new carboxylic acid and ester groups and a decrease in unsaturation. No evidence of tertiary carbons was found in C-13 135 degrees DEPT NMR spectra that would be characteristic of products of free radical vinyl polymerization, Diels-Alder reactions, or aldol condensation reactions. Thus, the data presented here suggest that esters are responsible for the majority of the polymerization reactions in this, and presumably other, aged/oxidized biodiesel fuel.
机译:大豆生物柴油在高温(90摄氏度)下通气老化,模拟柴油发动机燃料系统条件,产生了更高分子量的材料,并增加了运动粘度。除生物柴油脂肪酸甲酯(FAME)中的氧键外,还确定有相当一部分引入的氧为新的酯键。这项研究的目的是表征经过氧化的生物柴油燃料的高分子量成分,并通过将酯和醚键解聚的实验来了解酯对粘度增加的贡献。表征高分子量材料的方法包括酸和氧化生物柴油与甲醇的碱酯交换反应;用氢碘酸(HI)水解;老化和酯交换的材料的GC-MS,凝胶渗透色谱,FTIR和C-13 NMR。通过与NaOCH3或CH3OH / HCl的酯交换反应进行的解聚反应,特别是针对酯键的解聚反应,使老化的生物柴油的分子量分布和粘度显着降低。针对酯和醚键的HI解聚反应未显示分子量或运动粘度的进一步降低,这表明醚键的作用可忽略不计。 FTIR光谱表明,解聚处理后的羰基拉伸振动发生了变化,这与酯的参与一致。借助GC-MS,可在未处理的老化生物柴油中不存在的解聚产物中初步鉴定出二羧酸,这表明它在形成聚酯产品中起交联剂的作用。最后,C-13 NMR显示的数据与生物柴油发生重大氧化相一致,产生新的羧酸和酯基,并且不饱和度降低。在C-13 135度DEPT NMR光谱中没有发现叔碳的证据,叔碳是自由基乙烯基聚合,狄尔斯-阿尔德反应或羟醛缩合反应产物的特征。因此,此处提供的数据表明,酯是这种(大概是其他的)老化/氧化生物柴油燃料中大部分聚合反应的原因。

著录项

  • 来源
    《Energy & fuels》 |2018年第12期|12587-12596|共10页
  • 作者单位

    Ford Motor Co, Res & Adv Engn, Dearborn, MI 48124 USA;

    Ford Motor Co, Res & Adv Engn, Dearborn, MI 48124 USA;

    Ford Motor Co, Res & Adv Engn, Dearborn, MI 48124 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
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号