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Application of size exclusion electrochromatography to the microanalytical determination of the molecular mass distribution of celluloses from objects of cultural and historical value

机译:尺寸排阻电色谱法在具有文化和历史价值的物体的纤维素分子质量分布的微观分析中的应用

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The molecular mass distributions (MMD) of celluloses from paper and other sources were determined by size exclusion electrochromatography (SEEC). Prior to the separation the celluloses were chemically modified with phenyl isocyanate into their tricarbanilate derivatives (CTC). Sensitive UV detection of the CTC could be performed at a wavelength of 210 nm. The solvent used for separation was acetone. With this solvent, a high electroosmotic flow could be generated in columns packed with bare silica particles. With a column packed with particles with a nominal pore size of 30 nm, use of a mobile phase with a salt concentration of 0.1 mM was found to be optimal with respect to mass selectivity and efficiency. The workable mass range under these conditions was from 2 kDa to at least 500 kDa for (native) celluloses. The SEEC method was compared to classical pressure-driven size exclusion chromatography (PD-SEC). It is shown that the two methods give comparable results for the MMD of celluloses, while SEEC has important advantages in terms of speed and sample consumption. With SEEC, the analysis time was less than 20 min. The method was applied for the study of cellulose degradation during (artificial) aging of paper samples. A clear reduction of the average molecular mass of cellulose during aging was observed. With SEEC, the required sample amount is strongly reduced compared to classical PD-SEC. With a single paper fiber (after derivatization), multiple analyses could be carried out. It is argued that this is not only important for the analysis of unique objects but that it also allows the detection of MMD heterogeneities on a microscale. The strong reduction in sample size may be relevant when local heterogeneities in other types of polymer samples are studied. [References: 25]
机译:来自纸张和其他来源的纤维素的分子量分布(MMD)通过尺寸排阻电色谱法(SEEC)确定。在分离之前,将纤维素用异氰酸苯酯化学修饰成它们的三氨基甲酸酯衍生物(CTC)。可以在210 nm的波长下对CTC进行敏感的UV检测。用于分离的溶剂是丙酮。使用这种溶剂,可以在装有裸露二氧化硅颗粒的色谱柱中产生高电渗流。对于填充有标称孔径为30 nm的颗粒的色谱柱,发现在质量选择性和效率方面,使用盐浓度为0.1 mM的流动相是最佳的。在这些条件下,(天然)纤维素的有效质量范围为2 kDa至至少500 kDa。将SEEC方法与经典压力驱动式体积排阻色谱法(PD-SEC)进行了比较。结果表明,两种方法对纤维素的MMD给出了可比的结果,而SEEC在速度和样品消耗方面具有重要的优势。使用SEEC,分析时间不到20分钟。该方法用于研究纸样品(人工)老化过程中的纤维素降解。观察到老化期间纤维素的平均分子量明显降低。与经典的PD-SEC相比,使用SEEC可以大大减少所需的样本量。使用单根纸纤维(衍生化后),可以进行多次分析。有人认为,这不仅对独特对象的分析很重要,而且还允许在微尺度上检测MMD异质性。当研究其他类型的聚合物样品中的局部异质性时,样品量的大幅减少可能是相关的。 [参考:25]

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