水中锰离子交换效率与离子石类型、形态及其硬度的关系

M. Gomelya, I. Trus, M. Tverdokhlib, Viktor Kamaiev
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引用次数: 0

摘要

饮用水必须符合物理、化学、细菌学和放射化学准则,因此在进入分配系统之前应不断监测其质量。用于人类消费的水可能来自各种来源:地下水、泉水;来自河流、小溪、湖泊等的水。根据各种指标,乌克兰人口的很大一部分使用的饮用水不符合卫生要求。天然水体中经常存在锰化合物。它们的定量含量变化范围很广,根据地区不同,可为0、5-10 mg/dm3。值得注意的是,由于水中锰化合物含量高,去除它们是一项相当困难的任务。可以使用离子交换法从水中去除锰化合物,该方法包括通过盐或酸性形式的负载过滤水。同时,水的软化和淡化可以同时发生。因此,应采用离子交换法进行水的综合净化、软化和锰化合物的去除。本文介绍了用强酸性阳离子矿KU-2-8和弱酸性阳离子矿Dowex MAC-3从蒸馏水和自来水中提取锰离子的结果。阳离子以Na+和Ca2+形式使用。锰离子(Mn2+)浓度在5 ~ 500 mg/dm3之间变化。结果表明:cu -2-8的吸附能力与锰离子的浓度、离子的形态、水中硬度离子的存在有关,而与介质pH的关系不大。弱酸性阳离子矿的吸附量随锰离子浓度的增加和介质pH的增加而增加,随蒸馏水中硫酸镁浓度的变化而变化。与蒸馏水溶液相比,强酸性和弱酸性阳离子对自来水中锰离子的吸附减少,这与硬度离子的竞争性吸附有关。当在自来水溶液中使用Ca2+形式的离子离子时,这一点尤其明显。Ca2+形式离子离子的使用在一定程度上降低了它们对Mn2+和蒸馏水的吸附能力。但与自来水相比,这种影响较小。本文采用Thomas模型估算了弱酸性阳离子矿在低浓度MnSO4溶液中蒸馏水的全交换容量。
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The dependence of the efficiency of the ion exchange of manganese ions from water on the type and form of the ionite and its hardness
Drinking water must comply physical, chemical, bacteriological and radiochemical guidelines therefore its quality should be continuously monitored before being introduced into the distribution system. Water used for human consumption may come from various sources: groundwater, spring water; water from rivers, streams, lakes, among other. A large part of the population of Ukraine uses drinking water that does not meet hygienic requirements according to various indicators. Manganese compounds are quite often present in natural waters. Their quantitative content can vary in a wide range, depending on the region, it can be 0,5-10 mg/dm3. It is worth noting that with a high content of manganese compounds in water, their removal is a rather difficult task. Removal of manganese compounds from water can be implemented using the ion exchange method, which consists of filtering water through loading in salt or acidic form. At the same time, softening and desalination of water can occur simultaneously. Therefore, the ion exchange method should be used for comprehensive water purification, softening, and removal of manganese compounds. The article presents the results of obtained during the extraction of manganese ions from distilled and tap water using the strongly acidic cationite KU-2-8 and the weakly acidic cationite Dowex MAC-3. Cationites were used in Na+ and Ca2+ form. The concentration of manganese ions (Mn2+) was varied from 5 to 500 mg/dm3. It was shown that the sorption capacity of the cationite KU-2-8 depended on the concentration of manganese ions, the form of the ionite, the presence of hardness ions in water and was little dependent on the pH of the medium. The sorption capacity of the weakly acidic cationite increased with the increase in the concentration of manganese ions and with the increase in the pH of the medium, which changed with the change in the concentration of magnesium sulfate in distilled water. Sorption of manganese ions from tap water decreases for strongly acidic and weakly acidic cations, compared to solutions in distilled water, which is associated with competitive sorption of hardness ions. This is especially noticeable when using ionites in Ca2+ form in solutions in tap water. The use of ionites in Ca2+ form reduces their sorption capacity for Mn2+ and in distilled water to a certain extent. But this effect is smaller compared to tap water. The Thomas model was used in the work to estimate the full exchange capacity of weakly acidic cationite at low concentrations of MnSO4 solution in distilled water.
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