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通过马来酸酐衍生化,随后采用紫外可见检测的液相色谱法测定脂肪醇聚氧乙烯醚。

Determination of fatty alcohol ethoxylates by derivatisation with maleic anhydride followed by liquid chromatography with UV-vis detection.

作者信息

Micó-Tormos A, Collado-Soriano C, Torres-Lapasió J R, Simó-Alfonso E, Ramis-Ramos G

机构信息

Departament de Química Analítica, Universitat de València, Dr. Moliner 50, 46100 Burjassot, Spain.

出版信息

J Chromatogr A. 2008 Feb 8;1180(1-2):32-41. doi: 10.1016/j.chroma.2007.11.105. Epub 2007 Dec 7.

Abstract

The esterification of fatty alcohol ethoxylates (FAEs) by melting with maleic anhydride has been studied in the presence of urea. The reaction rate and yield of non-ethoxylated and ethoxylated alcohols increase largely when grinded urea is suspended in the reaction medium, a 100% yield being achieved at 80 degrees C in 15 min. The procedure is tolerant to the presence of large amounts of water. The UV-vis response factors of the derivatives of individual FAE oligomers vary little with the number of carbon atoms in the alkyl chain, n, and the number of ethylene oxide units, m. Derivatised samples of industrial FAE mixtures, cleaning products and river and sea waters were chromatographed on a C8 column of the fused-core type using gradient elution with acetonitrile/water mixtures plus 0.1% acetic acid. The hydrocarbon series with even values of n from 8 up to 20, were well resolved using column temperatures in the 15-30 degrees C range. Superior resolution between the consecutive oligomers within the series was also obtained at large values of m; however, reversion of the elution order for the derivatives with m=1 and 0 hindered direct quantitation of a few oligomers at low m values. Full resolution of all the oligomers was achieved by deconvolution with a genetic algorithm assisted by the unconstrained local method of Powell. After preconcentration with C18 solid-phase extraction cartridges, both river and sea water samples also showed the signature of the FAE oligomers. The evaluation of total FAEs in these samples was demonstrated.

摘要

在尿素存在的情况下,研究了脂肪醇乙氧基化物(FAE)与马来酸酐熔融酯化反应。当将研磨后的尿素悬浮于反应介质中时,未乙氧基化和乙氧基化醇的反应速率和产率大幅提高,在80℃下15分钟内可实现100%的产率。该方法能耐受大量水的存在。各个FAE低聚物衍生物的紫外可见响应因子随烷基链中碳原子数n和环氧乙烷单元数m的变化很小。使用乙腈/水混合物加0.1%乙酸进行梯度洗脱,在熔融核型C8柱上对工业FAE混合物、清洁产品以及河水和海水中的衍生化样品进行色谱分析。使用15 - 30℃范围内的柱温,n值从8到20的偶数碳氢化合物系列得到了很好的分离。在m值较大时,该系列中连续低聚物之间也获得了卓越的分离度;然而,m = 1和0的衍生物洗脱顺序的反转阻碍了低m值时少数低聚物的直接定量。通过使用鲍威尔无约束局部方法辅助的遗传算法进行去卷积,实现了所有低聚物的完全分离。在用C18固相萃取柱进行预浓缩后,河水和海水样品也显示出FAE低聚物的特征。展示了这些样品中总FAE的评估方法。

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