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Chemical factors affecting degradation processes of vegetable oils during frying.

机译:影响油炸过程中植物油降解过程的化学因素。

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摘要

Food oils degrade rapidly when exposed to high temperatures in frying, but the mechanisms responsible have never been fully elucidated. Thermal degradation is usually described as a combination of hydrolysis and accelerated autoxidation. Thermal scissions of lipid chains have also been identified but remain controversial and largely ignored. This research sought to elucidate the reactions underlying thermal degradation, reconcile roles of thermal scission and autoxidation, and determine where catalytic factors intervene in degradation at frying temperatures.;Thermal degradation processes were investigated in high oleic sunflower oil:corn oil blends (60:40 w/w) heated in an Oxipres(TM) oxygen bomb at 180°C for three hours under 2 bars (O2, air, or O2/N 2 blends) to determine rates and amounts of oxygen consumed during heating. Degradation products (conjugated dienes, peroxide values, aldehydes, free fatty acids) were measured in samples removed at various time intervals. In a parallel study, volatiles released during heating were trapped and analyzed by GC-MS. Effects of oil state and pre-oxidation were evaluated using stripped, fresh, and steady-state frying versions of the oil blend. Effects of oxygen, metals, water, phospholipids and free fatty acids were tested individually and in combinations to reveal synergistic catalysis of degradation.;Results supported thermal scission of lipid acyl chains as the dominant process controlling degradation at high temperatures, generating radicals that are the precursors for a broad range of downstream products. Terminal peroxyl radicals formed by addition of oxygen to thermal scission radicals abstract hydrogens from lipid chains to initiate autoxidation chains as a secondary process. Oxygen and water were the major forces driving secondary reactions. Traditional catalytic factors known to induce lipid oxidation had relatively minor effects alone but in combination with water triggered rapid consumption of O2. Except for oxygen, catalytic factors affected secondary oxidation processes and product distributions rather than initiating oxidation. Mismatch between O2 consumption and levels of oxidation products demonstrated presence of reaction pathways that consumed oxygen but led to products other than those measured.;Data was integrated to develop a new reaction scheme for thermal degradation of oils. Application of this new information can be used to improve stabilization of frying oils.
机译:食用油在高温下油炸时会迅速降解,但其作用机理尚未完全阐明。通常将热降解描述为水解和加速自氧化的结合。脂质链的热切割也已被发现,但仍存在争议,在很大程度上被忽略。这项研究试图阐明热降解的基本反应,调解和自氧化的作用,并确定在油炸温度下催化因素在降解中介入的位置。;在高油酸向日葵油:玉米油混合物中研究了热降解过程(60:40 w / w)在Oxipres(TM)氧弹中在2巴(O2,空气或O2 / N 2混合气)下于180°C加热3小时,以确定加热期间消耗的氧气的速率和数量。在不同时间间隔取出的样品中测量降解产物(共轭二烯,过氧化物,醛,游离脂肪酸)。在一项平行研究中,捕获了加热过程中释放的挥发物,并通过GC-MS分析。使用脱脂的,新鲜的和稳态油炸的油混合物评估油状态和预氧化的影响。分别测试了氧气,金属,水,磷脂和游离脂肪酸的影响,并进行了组合测试,以揭示降解的协同催化作用;结果支持脂酰基链的热断裂是控制高温降解的主要过程,并产生自由基。各种下游产品的前体。通过将氧添加到热断裂自由基上而形成的末端过氧自由基作为次要过程从脂质链中提取氢以引发自氧化链。氧气和水是驱动次级反应的主要力量。已知可诱导脂质氧化的传统催化因子单独作用相对较小,但与水结合可触发O2的快速消耗。除氧气外,催化因素影响二次氧化过程和产物分布,而不是引发氧化。 O2消耗量与氧化产物水平之间的不匹配表明存在消耗氧气但导致除测出的产物以外的产物的反应途径。数据已集成以开发用于油热降解的新反应方案。此新信息的应用可用于提高煎炸油的稳定性。

著录项

  • 作者

    Tian, Xin.;

  • 作者单位

    Rutgers The State University of New Jersey - New Brunswick.;

  • 授予单位 Rutgers The State University of New Jersey - New Brunswick.;
  • 学科 Agriculture Food Science and Technology.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 165 p.
  • 总页数 165
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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