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Review of Oxidative Processes in Wine and Value of Reduction Potentials in Enology

机译:葡萄酒中的氧化过程及其在葡萄酒中的还原潜力

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The reduction potential of wines has been thought to indicate their level of oxidation or reduction, but how that relates to wine composition has remained vague. Reduction potentials are generated by redox couples, which are at equilibrium and both adsorbed on the measuring electrode, the magnitude of the potential for any couple being determined by the relative proportion of the oxidized and reduced component. However, redox couples associated with polyphenols, which are most likely to determine reduction potentials, are not at equilibrium in wine due to the instability of quinones. Reduction potentials are highly dependent on oxygen concentration and it is proposed that they are generated by the oxidation of ethanol coupled to the reduction of protons or of oxygen. While the so-called reduction potential is therefore of little value for wine, cyclic voltammetry has proved very useful in determining the reduction potential of wine constituents and estimating the concentration of the most readily reduced polyphenols. The reduction potentials of proposed redox couples involved in the reduction of oxygen and oxidation of polyphenols, ethanol, and sulfite are useful in determining the thermodynamic feasibility of possible interactions. The reaction of polyphenols with oxygen is mediated by iron, which redox cycles between them assisted by copper. Catechol-quinone and oxygen-hydrogen peroxide couples have similar reduction potentials. Consequently, the oxidation of catechols such as (+)-catechin cannot proceed to completion and is accelerated by substances that react with quinones, such as sulfite, which reduces them back to polyphenols. Sulfite, therefore, has multiple antioxidant activities. It accelerates oxygen consumption, prevents loss of polyphenols by regenerating them, and intercepts hydrogen peroxide, thus preventing ethanol oxidation.
机译:人们认为葡萄酒的还原潜力表明了其氧化或还原的水平,但与葡萄酒成分的关系仍不清楚。还原电势由处于平衡状态且均吸附在测量电极上的氧化还原对产生,任何一对电势的大小均取决于被氧化和还原的组分的相对比例。但是,由于醌类的不稳定性,与多酚相关的氧化还原对最有可能确定还原电位,因此在葡萄酒中并未达到平衡。还原电势高度依赖于氧浓度,并且提出它们是通过乙醇的氧化与质子或氧气的还原相结合而产生的。因此,尽管所谓的还原电位对葡萄酒几乎没有价值,但是循环伏安法已被证明在确定葡萄酒成分的还原电位和估计最易还原的多酚的浓度方面非常有用。拟议的氧化还原对的还原电位涉及氧气的还原以及多酚,乙醇和亚硫酸盐的氧化,可用于确定可能发生相互作用的热力学可行性。多酚与氧的反应由铁介导,铁之间的氧化还原循环在铜的辅助下进行。邻苯二酚醌和过氧化氢氧对具有相似的还原电位。因此,邻苯二酚(如(+)-儿茶素)的氧化无法继续完成,而会与与醌反应的物质(如亚硫酸盐)加速氧化,从而将它们还原成多酚。因此,亚硫酸盐具有多种抗氧化活性。它加快了氧气消耗,通过再生多酚防止了多酚的损失,并拦截了过氧化氢,从而防止了乙醇的氧化。

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