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采用核磁共振氢谱法对苹果酒中丙烯醛进行定量测定。

Quantitative Determination of Acrolein in Cider by H NMR Spectrometry.

作者信息

de Las Heras Enaitz, Zuriarrain-Ocio Andoni, Zuriarrain Juan, Bordagaray Ane, Dueñas María Teresa, Berregi Iñaki

机构信息

Faculty of Chemistry, University of the Basque Country EHU/UPV, 20018 Donostia-San Sebastián, Spain.

出版信息

Foods. 2020 Dec 8;9(12):1820. doi: 10.3390/foods9121820.

Abstract

Acrolein occasionally appears in cider, completely spoiling its quality due to its bitter taste. It is crucial to detect it in the early steps, before the taste is severely affected, to apply the appropriate treatment. A simple and rapid analytical method to determine this compound in cider is therefore desirable. In this work, a quantitative determination method of acrolein in cider is proposed using the proton nuclear magnetic resonance technique (H NMR). Acrolein produces a doublet signal in the spectrum at 9.49 ppm, whose area is used to determine the concentration of this compound. Importantly, 3-(Trimethylsilyl)-2,2,3,3-d-propionic acid sodium salt is added to the cider as a reference for 0.00 ppm and 1,3,5-benzenetricarboxylic acid as an internal standard for acrolein determination. The method is validated by gas chromatography (GC). There is a good correlation between the acrolein concentrations obtained by H NMR and by gas chromatography in different commercial ciders (Pearson coefficient 0.9994). The 95% confidence interval for the intercept is 0.15 ± 0.49 (includes 0) and for the slope is 0.98 ± 0.03 (includes 1). When applying the paired test, no significant difference is observed. The proposed method is direct, and no prior derivatization is needed.

摘要

丙烯醛偶尔会出现在苹果酒中,因其苦味会完全破坏苹果酒的品质。在味道受到严重影响之前的早期阶段检测到它,以便采取适当的处理措施至关重要。因此,需要一种简单快速的分析方法来测定苹果酒中的这种化合物。在这项工作中,提出了一种使用质子核磁共振技术(¹H NMR)测定苹果酒中丙烯醛的定量方法。丙烯醛在光谱中9.49 ppm处产生双峰信号,其面积用于确定该化合物的浓度。重要的是,将3-(三甲基硅基)-2,2,3,3-d-丙酸三钠盐作为0.00 ppm的内标添加到苹果酒中,并将1,3,5-苯三甲酸作为测定丙烯醛的内标。该方法通过气相色谱(GC)进行验证。在不同市售苹果酒中,¹H NMR和气相色谱法测得的丙烯醛浓度之间存在良好的相关性(皮尔逊系数为0.9994)。截距的95%置信区间为0.15±0.49(包括0),斜率的95%置信区间为0.98±0.03(包括1)。应用配对检验时,未观察到显著差异。所提出的方法是直接的,无需预先衍生化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aa6/7762539/9f51940df917/foods-09-01820-g001.jpg

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