2.2
惰性离子化合物的添加增加了微溶盐的溶解度。例如,将硝酸钾添加到硫酸钙的饱和溶液中可显著提高硫酸钙的溶解度。勒夏特列原理则无法预测这种均衡的转变。相反,这可以用添加惰性盐时溶液中离子有效浓度的变化来进行解释。
在该溶液中,主要阳离子(钙离子)被主要阴离子(硫酸根离子)包围,而硫酸根离子则又被钙离子所包…
将 50 mmol 硝酸钾加入 1 升饱和的硫酸钙水溶液中,会导致溶解的钙离子和硫酸根离子浓度增加约 30%。
除了已存在的抗衡离子外,所添加的惰性盐(硝酸钾)中的相反电荷离子也会参与形成围绕主要阳离子和阴离子的离子氛。
因此,钙离子和硫酸根离子的净电荷减少,导致它们之间的吸引力减弱。因此,溶解平衡向解离的离子方向移动。
这种阳离子和阴离子相互结合的趋势降低,体现在它们在溶液中浓度的增加,从而提高了微溶硫酸钙的溶解度。
溶液的离子强度越高,离子氛所带电荷越大,盐解离成离子的程度也越大。
这种现象被称为盐效应、电解质效应或多元离子效应。
这种效应在组成离子电荷较高的微溶盐中更为显著。
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Q1: What happens to calcium sulfate solubility when potassium nitrate is added to the solution?
Adding potassium nitrate to a saturated calcium sulfate solution increases the solubility of calcium sulfate by approximately 30%. The inert salt's ions form ionic atmospheres around the primary calcium and sulfate ions, reducing their net charges and weakening the electrostatic attraction between them. This shift toward dissociated ions enhances solubility, a phenomenon known as the salt effect or diverse ion effect.
Q2: Why does Le Châtelier's principle fail to predict the solubility increase from added inert salt?
Le Châtelier's principle cannot predict this equilibrium shift because adding an inert salt like potassium nitrate does not change the concentration of the primary ions directly. Instead, the effect arises from changes in the effective concentration and ionic atmospheres surrounding calcium and sulfate ions, reducing their net charges and altering the equilibrium through activity rather than stoichiometric concentration changes.
Q3: How do ionic atmospheres affect the net charge on primary ions in solution?
Ionic atmospheres form around each primary ion, consisting of oppositely charged ions from both the original salt and the added inert compound. These surrounding ions shield the primary ion's charge, causing its net charge to decrease. The reduced net charge weakens electrostatic attraction between cations and anions, promoting dissociation and increasing solubility of the sparingly soluble salt.
Q4: How does ionic strength influence the magnitude of the salt effect?
Higher ionic strength produces a greater salt effect because more ions diffuse into the ionic atmosphere surrounding primary ions. This increased ion concentration further reduces the net charge on primary ions, facilitating greater dissociation of the salt. The relationship is direct: as ionic strength increases, the dissociation of sparingly soluble salts becomes more pronounced.
Q5: Why do doubly charged ions show a stronger salt effect than singly charged ions?
Doubly charged ions, such as those in barium sulfate, experience a more pronounced salt effect than singly charged ions like those in silver chloride when exposed to the same concentration of inert salt. The higher charge density on doubly charged ions creates stronger electrostatic interactions that are more significantly affected by the shielding effect of ionic atmospheres, resulting in greater solubility enhancement.
Q6: What is the relationship between ionic strength and the dissociation of sparingly soluble salts?
The salt effect depends critically on ionic strength. As ionic strength increases, more ions populate the ionic atmosphere, progressively lowering the net charge on primary ions and reducing precipitation frequency. This direct relationship means that higher ionic strength solutions promote greater dissociation of sparingly soluble salts, shifting the solubility equilibrium toward dissolved ions.
Q7: How do the ions from an inert compound contribute to changes in solubility equilibrium?
Ions from inert compounds like potassium nitrate surround primary ions, forming part of their ionic atmospheres. These oppositely charged ions reduce the effective charge on primary cations and anions, decreasing electrostatic attraction between them. This charge reduction shifts the solubility equilibrium toward dissociated ions, increasing the concentration of dissolved calcium and sulfate ions in solution.