首页> 外文期刊>Macromolecular chemistry and physics >Adsorption and enthalpic partition in liquid chromatography of non-charged synthetic polymers, 3 - Interphase adsorption versus enthalpic partition of polystyrene in alkane-bonded silica gel
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Adsorption and enthalpic partition in liquid chromatography of non-charged synthetic polymers, 3 - Interphase adsorption versus enthalpic partition of polystyrene in alkane-bonded silica gel

机译:不带电荷的合成聚合物在液相色谱中的吸附和焓分配,烷烃键合硅胶中3-苯乙烯的相间吸附与焓分配

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摘要

Two kinds of retention mechanisms of polystyrene (PS) macromolecules are considered in liquid chromatography (LC) applying alkane-bonded silica gel phases as column packings. They are based on non-polar interactions between polymer segments and alkane groups, which lead to adsorption of polymer species on the surface situated between bonded alkane groups and eluent on the the hand (interphase adsorption) and to partition of macromolecules between bonded phase volume and eluent (enthalpic partition) on the other hand. The roles of both retention mechanisms were assessed for PS species with different molar masses and several series of binary eluents. Bare silica and C-1, C-4, C-8, as well as C-18-bonded phases were compared. The results demonstrated that the eluent had to be a thermodynamically poor solvent for macromolecules to push them onto/into the bonded phase. However, no quantitative dependence between the eluent's thermodynamic quality for macromolecules and the extent of retention of polymer species was found. Similarly, no correlation was identified between eluent quality and prevailing retention mechanism - either interphase adsorption on the trimethyl-silylated silica gel or interphase adsorption plus enthalpic partition in the case of C-4, C-8 and C-18-bonded phases. The explanation is to be sought in the actual "composition" of the preferentially solvated macromolecules and bonded alkane groups. the bonded phase probably has to be a slightly better "solvent" than the eluent for a polymer species to cause their retention. Enthalpic partition of PS plays an especially important role in DMF/THF mixed eluents. The results indicate, however, that only three to five terminal -CH2- groups plus the methyl end-group take part in the enthalpic partition process. the means that silica gel bonded with shorter alkane groups may be advantageous compared to the C-18 packings in some coupled high performance liquid chromatography methods for synthetic polymers, combining entropic and enthalpic retention mechanisms.
机译:在液相色谱(LC)中考虑了两种聚苯乙烯(PS)分子的保留机理,该色谱采用烷烃键合的硅胶相作为色谱柱填料。它们基于聚合物链段与烷烃基团之间的非极性相互作用,这导致聚合物物种吸附在位于键合烷烃基团之间的表面和手上的洗脱液上(相间吸附),并使大分子在键合相体积与另一方面,洗脱液(焓分区)。评估了两种保留机制对具有不同摩尔质量和几种系列二元洗脱液的PS物种的作用。比较了裸二氧化硅和C-1,C-4,C-8以及C-18键合的相。结果表明,洗脱液必须是大分子的热力学不良溶剂,才能将其推入键合相或推入键合相。但是,在洗脱液的大分子热力学质量与聚合物种类的保留程度之间未发现定量依赖性。同样,在洗脱液质量和主要的保留机理之间也没有发现相关性-在C-4,C-8和C-18键合相的情况下,相间吸附在三甲基甲硅烷基化硅胶上,或者相间吸附加焓分配。在优先溶剂化的大分子和键合的烷烃基团的实际“组成”中寻求解释。对于聚合物种类而言,键合相可能必须比洗脱液略好一些,以引起聚合物的保留。 PS的焓分配在DMF / THF混合洗脱液中起特别重要的作用。然而,结果表明,仅三至五个末端-CH 2-基团加上甲基末端基团参与了焓分配过程。这意味着在结合了熵和焓保留机制的合成聚合物的某些高效液相色谱方法中,与较短的烷烃基键合的硅胶与C-18填料相比可能更具优势。

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