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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Quantitative analysis of an oligomeric hindered amine light stabilizer in polypropylene by matrix-assisted laser desorption/ionization mass spectrometry using a solid sampling technique
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Quantitative analysis of an oligomeric hindered amine light stabilizer in polypropylene by matrix-assisted laser desorption/ionization mass spectrometry using a solid sampling technique

机译:固相采样技术通过基质辅助激光解吸/电离质谱对聚丙烯中的低聚受阻胺光稳定剂进行定量分析

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摘要

A small amount of an oligomeric hindered amine light stabilizer (HALS) (Adekastab LA-68LD) in polypropylene (PP) materials was directly determined by solid sampling matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) using an internal standard method. First the matrix reagent (dithranol), 20 mg, and the empirically selected internal standard, angiotensin I (MW = 1296.5), 5 mu g, were premixed in the solid state. The matrix mixture was then co-ground with the PP sample containing the HALS in liquid nitrogen using a freezer mill. The powdered sample mixture was spotted on the sample plate, suspended in ion-exchanged water, dried to adhere on the plate, and subjected to MALDI-MS. Three series of the HALS components accompanied by the oxidized species were clearly observed as their molecular ions (M.+) along with that of the internal standard in the mass spectra. A fairly good linear relationship (R-2 = 0.9991) with a relative standard deviation of ca. 11% was observed between the relative peak intensities of the HALS components and the HALS contents ranging from 0.1-2.5 wt%, which could be used as the calibration line to determine the HALS content in PP composites directly by MALDI-MS. The UV-exposed PP composite samples were evaluated by this method to interpret the photostabilizing action of HALS in the PP materials based on the observed change in the relative abundances of the original and oxidized HALS components as a function of UV-exposure time. Copyright (c) 2006 John Wiley & Sons, Ltd.
机译:聚丙烯(PP)材料中的少量低聚受阻胺光稳定剂(HALS)(Adekastab LA-68LD)使用内标方法通过固体样品基质辅助激光解吸/电离质谱(MALDI-MS)直接测定。首先,将20毫克基质试剂(二乙醇胺)和5克根据经验选择的内标血管紧张素I(分子量= 1296.5)预混。然后使用冷冻磨将基质混合物与含有HALS的PP样品在液氮中共研磨。将粉末状的样品混合物点样在样品板上,悬浮在离子交换水中,干燥以粘附在板上,然后进行MALDI-MS处理。质谱图中清楚地观察到伴随着氧化物质的三个系列的HALS组分及其分子离子(M. +)和内标物的分子离子(M. +)。相对良好的线性关系(R-2 = 0.9991),相对标准偏差为。在HALS组分的相对峰强度与HALS含量在0.1-2.5 wt%之间的范围内观察到11%的含量,这可以用作通过MALDI-MS直接测定PP复合材料中HALS含量的校准线。通过这种方法评估了紫外线暴露的PP复合材料样品,以根据观察到的原始HALS组分和氧化后的HALS组分的相对丰度随紫外线暴露时间的变化来解释HALS在PP材料中的光稳定作用。版权所有(c)2006 John Wiley&Sons,Ltd.

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