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Characterization and analysis of non-ionic surfactants by supercritical fluid chromatography combined with ion mobility spectrometry-mass spectrometry

机译:超临界流体色谱结合离子迁移光谱 - 质谱法,对非离子表面活性剂的表征及分析

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Comprehensive separation and analysis of non-ionic surfactants have been conducted by coupling supercritical fluid chromatography (SFC) with ion mobility spectrometry-mass spectrometry (IMS-MS). Representative non-ionic surfactants were investigated, including alkylphenol ethoxylates (APEOs), e.g., octylphenol ethoxylates (OPEOs) and fatty alcohol ethoxylates (FAEs), e.g., lauryl alcohol ethoxylates (LAEs). A sub-2-m high-density diol column was used for chromatographic separation by the first-dimensional SFC due to the differences in ethoxy chain prior to electrospray ionization (ESI). Maintaining the fidelity of pre-ionization separation in the first dimension, the introduction of IMS provided additional post-ionization resolution by broadly fractionating the oligometric ethoxymers based on their size and electric charge within 13.78ms. Distinguishable series of singly and multiply charged non-ionic species could be clearly observed. The millisecond timescale ion mobility separation perfectly fits the elution time of a chromatographic peak, while effectively feeding components into the fast-scanning time-of-flight (TOF) mass analyzer for characterization and analysis. The orthogonality of the developed separation and analysis system was evaluated, revealing a correlation coefficient and peak spreading angle of 0.2729 and 74.16 degrees for the studied OPEOs and 0.1962 and 78.69 degrees for LAEs. Significant enhancement in peak capacity was achieved for the developed SFC-IMS-MS system with the actual peak capacity measured to be approximately 41 and 160 times higher than that of the dimensions of SFC and IMS, respectively, when used alone
机译:通过将超临界流体色谱(SFC)与离子迁移率光谱 - 质谱(IMS-MS)偶联,通过耦合超临界流体色谱(SFC)进行综合分离和分析。研究了代表性的非离子表面活性剂,包括烷基酚乙氧基化物(APEOS),例如辛基苯酚乙氧基化物(OPEOS)和脂肪醇乙氧基化物(FEES),例如月桂醇乙氧基化物(Laes)。由于电喷雾电离(ESI)之前,通过第一维SFC用于通过第一维SFC进行色谱分离的亚2M高密度二醇塔。在第一尺寸中保持预电离分离的保真度,通过基于其尺寸和电荷在13.78ms内的尺寸和电荷的大小分馏,IMS的引入提供了额外的电离后分辨率。可以清楚地观察到单独和繁殖的非离子物质的可区分系列。毫秒秒的离子迁移率分离完美地适合色谱峰的洗脱时间,同时有效地将组件送入快速扫描飞行时间(TOF)质量分析仪以表征和分析。评估了开发的分离和分析系统的正交性,揭示了研究的OPEOS和0.1962和78.69度的0.2729和74.16度的相关系数和峰值扩散角。对于显影的SFC-IMS-MS系统实现了峰值容量的显着增强,其实际峰值容量分别在单独使用时分别比SFC和IMS的尺寸高约41和160倍。

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