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Reaction enthalpy from the binding of multivalent cations to anionic polyelectrolytes in dilute solutions

机译:从多价阳离子结合到稀溶液中阴离子聚电解质的反应焓

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Dilute solutions of sodium poly(styrene sulfonate) (NaPSS) in the presence of Al3+, Ca2+, and Ba2+ were analysed by means of isothermal titration calorimetry (ITC) in order to investigate the heat effect of bond formation between those cations and the anionic SO3- residues of NaPSS. The selection of the cations was guided by the solution behavior of the corresponding PSS salts from a preceding study [M. Hansch et al., J. Chem. Phys. 148(1), 014901 (2018)], where bonds between Ba2+ and anionic PSS showed an increasing solubility with decreasing temperature and Al3+ exhibited the inverse trend. Unlike to Al3+ and Ba2+, Ca2+ is expected to behave as a purely electrostatically interacting bivalent cation and was thus included in the present study. Results from ITC satisfactorily succeeded to explain the temperature-dependent solution behavior of the salts with Al3+ and Ba2+ and confirmed the non-specific behavior of Ca2+. Additional ITC experiments with salts of Ca2+ and Ba2+ and sodium poly(acrylate) complemented the results on PSS by data from a chemically different polyanion. Availability of these joint sets of polyanion-cation combinations not only offers the chance to identify common features and subtle differences in the solution behavior of polyelectrolytes in the presence of multi-valent cations but also points to a new class of responsive materials. Published by AIP Publishing.
机译:通过等温滴定热量法(ITC)分析在Al3 +,Ca2 +和Ba2 +存在下稀释钠(苯乙烯磺酸盐)(酸丁酸酯)(滴定)的溶液,以研究这些阳离子和阴离子SO3之间的键形成的热效应 - 水滴的残留物。通过前述研究中的相应PSS盐的溶液行为引导阳离子的选择[M。 Hansch等人。,J.Chem。物理。 148(1),014901(2018)],其中Ba2 +和阴离子PS之间的键显示出随温度降低的溶解度越来越大,Al3 +表现出逆趋势。与Al3 +和Ba2 +不同,Ca2 +预期表现为纯粹静电相互作用的二价阳离子,因此包括在本研究中。 ITC的结果令人满意地成功地解释了用Al3 +和Ba2 +盐的温度依赖性溶液行为,并确认了Ca2 +的非特异性行为。额外的ITC实验,具有Ca2 +和Ba2 +和Polylium(丙烯酸酯)的盐通过来自化学不同的聚沉变的数据将PSS的结果互补。这些联合阳离子组合的可用性不仅提供了识别多价阳离子存在的聚电解质解决方案行为的共同特征和微妙差异,而且还指向一类新的响应材料。通过AIP发布发布。

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