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电解质水溶液的表面张力:与离子水合、氧溶解度和气泡聚并的关系

Surface Tension of Aqueous Solutions of Electrolytes: Relationship with Ion Hydration, Oxygen Solubility, and Bubble Coalescence.

作者信息

Weissenborn PK, Pugh RJ

机构信息

Institute for Surface Chemistry, Thin Films Group, Stockholm, S-114 86, Sweden

出版信息

J Colloid Interface Sci. 1996 Dec 25;184(2):550-63. doi: 10.1006/jcis.1996.0651.

Abstract

The surface tension of aqueous solutions of simple inorganic electrolytes (36 in total) have been measured by the maximum bubble pressure method as a function of electrolyte concentration up to 1 M. In most cases the surface tension increased, however in a minority of cases, certain combinations of cations and anions had a negligible effect or decreased surface tension. Results were analysed in terms of surface tension/electrolyte concentration gradients (d(Deltagamma)/dc) and this parameter was found to correlate with the entropies of ion hydration, Jones-Dole viscosity coefficients and dissolved oxygen gradients. Calculation of Gibbs surface deficiencies for selected electrolytes were carried out using the raw surface tension data. Discussion of the surface tension/electrolyte concentration gradients was extended to the mechanism of inhibition of bubble coalescence by electrolytes. The Gibbs-Marangoni effect did not provide a satisfactory explanation for the inhibition of coalescence for all electrolytes and from the present study we suggest that dissolved gas (microbubble) gradients between macroscopic bubbles plays an important role in the coalescence process.

摘要

采用最大气泡压力法,测量了简单无机电解质水溶液(共36种)的表面张力,该表面张力是电解质浓度高达1M时的函数。在大多数情况下,表面张力增加,然而在少数情况下,某些阳离子和阴离子的组合对表面张力的影响可忽略不计或使其降低。根据表面张力/电解质浓度梯度(d(Δγ)/dc)对结果进行了分析,发现该参数与离子水化熵、琼斯-多尔粘度系数和溶解氧梯度相关。利用原始表面张力数据,对选定电解质的吉布斯表面亏缺进行了计算。对表面张力/电解质浓度梯度的讨论扩展到了电解质对气泡聚并的抑制机制。吉布斯-马兰戈尼效应并不能对所有电解质的聚并抑制提供令人满意的解释,从本研究中我们认为,宏观气泡之间的溶解气体(微气泡)梯度在聚并过程中起着重要作用。

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