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聚合物的定量液相色谱-质谱联用:通过尺寸排阻色谱和电喷雾质谱联用及最大熵数据处理测定精确的分子量分布

Quantitative LC-MS of polymers: determining accurate molecular weight distributions by combined size exclusion chromatography and electrospray mass spectrometry with maximum entropy data processing.

作者信息

Gruendling Till, Guilhaus Michael, Barner-Kowollik Christopher

机构信息

Centre for Advanced Macromolecular Design, School of Chemical Sciences and Engineering, The University of New South Wales, Sydney, NSW 2033, Australia.

出版信息

Anal Chem. 2008 Sep 15;80(18):6915-27. doi: 10.1021/ac800591j. Epub 2008 Aug 9.

DOI:10.1021/ac800591j
PMID:18690749
Abstract

We report on the successful application of size exclusion chromatography (SEC) combined with electrospray ionization mass spectrometry (ESI-MS) and refractive index (RI) detection for the determination of accurate molecular weight distributions of synthetic polymers, corrected for chromatographic band broadening. The presented method makes use of the ability of ESI-MS to accurately depict the peak profiles and retention volumes of individual oligomers eluting from the SEC column, whereas quantitative information on the absolute concentration of oligomers is obtained from the RI-detector only. A sophisticated computational algorithm based on the maximum entropy principle is used to process the data gained by both detectors, yielding an accurate molecular weight distribution, corrected for chromatographic band broadening. Poly(methyl methacrylate) standards with molecular weights up to 10 kDa serve as model compounds. Molecular weight distributions (MWDs) obtained by the maximum entropy procedure are compared to MWDs, which were calculated by a conventional calibration of the SEC-retention time axis with peak retention data obtained from the mass spectrometer. Comparison showed that for the employed chromatographic system, distributions below 7 kDa were only weakly influenced by chromatographic band broadening. However, the maximum entropy algorithm could successfully correct the MWD of a 10 kDa standard for band broadening effects. Molecular weight averages were between 5 and 14% lower than the manufacturer stated data obtained by classical means of calibration. The presented method demonstrates a consistent approach for analyzing data obtained by coupling mass spectrometric detectors and concentration sensitive detectors to polymer liquid chromatography.

摘要

我们报道了尺寸排阻色谱法(SEC)结合电喷雾电离质谱法(ESI-MS)和折光指数(RI)检测在测定合成聚合物精确分子量分布方面的成功应用,该方法对色谱峰展宽进行了校正。所提出的方法利用了ESI-MS准确描绘从SEC柱洗脱的各个低聚物的峰形和保留体积的能力,而低聚物绝对浓度的定量信息仅从RI检测器获得。基于最大熵原理的复杂计算算法用于处理两个检测器获得的数据,从而得到校正了色谱峰展宽的准确分子量分布。分子量高达10 kDa的聚甲基丙烯酸甲酯标准品用作模型化合物。将通过最大熵程序获得的分子量分布(MWD)与通过使用从质谱仪获得的峰保留数据对SEC保留时间轴进行常规校准而计算得到的MWD进行比较。比较结果表明,对于所采用的色谱系统,7 kDa以下的分布仅受色谱峰展宽的微弱影响。然而,最大熵算法能够成功校正10 kDa标准品的MWD以消除峰展宽效应。分子量平均值比通过经典校准方法获得的制造商声明数据低5%至14%。所提出的方法展示了一种用于分析通过将质谱检测器和浓度敏感检测器与聚合物液相色谱联用而获得的数据的一致方法。

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