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首页> 外文期刊>American journal of enology & viticulture >Mechanism of Autoxidation of Polyphenols and Participation of Sulfite in Wine: Key Role of Iron
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Mechanism of Autoxidation of Polyphenols and Participation of Sulfite in Wine: Key Role of Iron

机译:葡萄酒中多酚的自氧化机理和亚硫酸盐的参与:铁的关键作用

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摘要

The involvement of iron (Fe) in the reaction of wine with oxygen was deduced at least 80 years ago. It was observed that when wine was exposed to air, some O2 reacted rapidly, in part to oxidize the Fe to the ferric state and in part to generate what were thought to be unstable peroxides. It was proposed that it was these intermediate oxidants that oxidized wine polyphenols. In this present work the oxidation of (+)-catechin was reexamined in model wine to determine if different phases of oxidation could be observed. In the absence of sulfite, after an initial uptake of O2 very little further reaction occurred. This initial O2 uptake increased with increasing concentrations of Fe(II) and Cu(II), indicating that Fe was the initial reactant and furthermore was absent when Fe was added as Fe(III). In contrast, in the presence of sulfite, the oxidation of (+)-catechin was markedly accelerated and, again, an initial more rapid phase of oxidation, presumably due to the metals, was discernable. With (+)-catechin, insufficient O2 to oxidize all the Fe was initially taken up and formation of other oxidants such as peroxides was unlikely. Further evidence is presented that nucleophiles such as sulfite accelerate oxidation by reacting with quinones. The rate of oxidation in the presence of sulfite was found to increase in the order (+)-catechin< caffeic acid< (-)-epicatechin < gallic. It is proposed that the rate of oxidation is determined by the relative reactivity of their respective quinones. In the absence of sulfite, these additional phenols were also oxidized extremely slowly. The initial faster phase of oxidation was also observed in a white wine
机译:至少在80年前就推断出铁(Fe)参与葡萄酒与氧气的反应。据观察,当葡萄酒暴露于空气中时,一些氧气会迅速反应,部分将铁氧化为三价铁,部分生成不稳定的过氧化物。有人提出,正是这些中间氧化剂氧化了葡萄酒中的多酚。在本工作中,对模型酒中(+)-儿茶素的氧化进行了重新检查,以确定是否可以观察到不同的氧化相。在不存在亚硫酸盐的情况下,最初吸收O2后几乎没有进一步的反应发生。最初的O2吸收随着Fe(II)和Cu(II)浓度的增加而增加,表明Fe是初始反应物,并且当添加Fe作为Fe(III)时则不存在。相反,在亚硫酸盐的存在下,(+)-儿茶素的氧化被显着加速,并且再次可以看出,可能是由于金属引起的初始的较快速的氧化阶段。使用(+)-儿茶素时,最初吸收的O2不足以氧化所有的Fe,不太可能形成其他氧化剂,例如过氧化物。进一步的证据表明,亲核试剂(如亚硫酸盐)通过与醌反应来加速氧化。发现在亚硫酸盐存在下的氧化速率以(+)-儿茶素<咖啡酸<(-)-表儿茶素<没食子酸>的顺序增加。提出氧化速率由它们各自的醌的相对反应性决定。在没有亚硫酸盐的情况下,这些额外的酚也被非常缓慢地氧化。在白葡萄酒中也观察到初始的较快的氧化阶段

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