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Molecular Weight Determination of Block Copolymers by Pulsed Gradient Spin Echo NMR

机译:脉冲梯度自旋回波核磁共振法测定嵌段共聚物的分子量

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摘要

Matrix-assisted laser desorption/ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS) is the technique of choice to achieve molecular weight data for synthetic polymers. Because the success of a MALDI-MS analysis critically depends on a proper matrix and cation selection, which in turn relates closely to the polymer chemical nature and size, prior estimation of the polymer size range strongly helps in rationalizing MALDI sample preparation. We recently showed how pulsed gradient spin echo (PGSE) nuclear magnetic resonance could be used as an advantageous alternative to size exclusion chromatography, to rationalize MALDI sample preparation and confidently interpret MALDI mass spectra for homopolymers. Our aim here is to extend this methodology to the demanding case of amphiphilic block copolymers, for which obtaining prior estimates on the M_(w) values appears as an even more stringent prerequisite. Specifically, by studying poly(ethylene oxide) polystyrene block copolymers of distinct molecular weights and relative block weight fractions, we show how PGSE data can be used to derive the block M_(w) values. In contrast to homopolymers, such determination requires not only properly recorded calibration curves for each of the polymers constituting the block copolymers but also an appropriate hydrodynamic model to correctly interpret the diffusion data.
机译:基质辅助激光解吸/电离(MALDI)飞行时间(TOF)质谱(MS)是获得合成聚合物分子量数据的首选技术。由于MALDI-MS分析的成功关键取决于适当的基质和阳离子选择,而这又与聚合物的化学性质和尺寸密切相关,因此,对聚合物尺寸范围的事先估算在很大程度上有助于合理化MALDI样品的制备。我们最近展示了如何将脉冲梯度自旋回波(PGSE)核磁共振用作尺寸排阻色谱的一种有利替代方案,以合理化MALDI样品制备并自信地解释均聚物的MALDI质谱图。我们的目标是将这种方法扩展到两亲性嵌段共聚物的苛刻情况,对于这种情况,获得M_(w)值的先前估计似乎是更为严格的前提。具体来说,通过研究具有不同分子量和相对嵌段重量分数的聚(环氧乙烷)聚苯乙烯嵌段共聚物,我们展示了如何使用PGSE数据得出嵌段M_(w)值。与均聚物相比,这种确定不仅需要正确记录构成嵌段共聚物的每种聚合物的校准曲线,而且需要适当的流体动力学模型以正确解释扩散数据。

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