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How to remove sulfate ions?

2015-09-10View Original

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To remove a small amount of sulfate ions in an alkaline or acidic environment, an hydrofluoric acid solution is used in acidic conditions, while a fluoride-containing ammonia solution is used in alkaline conditions. The concentrations of sulfate ions are 2 g/L, 25 g/L, and 280 g/L. How can these ions be removed effectively? I found that barium sulfate has the lowest solubility product, on the order of -10; so which barium salt would be suitable to use? Barium carbonate, barium chloride, barium fluoride, barium oxide, barium hydroxide, … Please experts analyze this: from a process perspective, what method is the most feasible and easy to control in terms of operation?
Reply #22015-09-11
If no requirements are imposed on the pH value, barium oxide or barium hydroxide can be used, without introducing any new anions
Reply #32015-09-11
In industry, barium chloride is generally used for removing sulfate ions, as it is cost-effective, efficient, and requires a small amount. For example, in the chlor-alkali industry, sulfate ions in brine can be removed very thoroughly.
Reply #42015-09-11
An acidic environment with barium fluoride and barium oxide; barium hydroxide is also a good option. It depends on whether your solution allows the introduction of new ions
Reply #52015-09-14
Thank you, but these chloride ions of mine will also affect the product quality.
Reply #62015-09-14
Thank you. The introduction of new ions may have an impact on product quality; I would still choose barium oxide and barium hydroxide, as well as barium fluoride. However, these are all substances that are insoluble in water. Will this lead to the consumption of F- ions? Could barium sulfate be formed directly on the surface of these solids? I wonder if such a situation could occur. On the surfaces of these insoluble particles, there is relatively high solubility; the farther away from the surface, the lower the solubility. A concentration gradient exists, with the highest concentration at the particle surface, which makes it easy for barium sulfate to form there, resulting in the particles being coated by precipitates. Would this increase the amount of material consumed? I hope the experts can provide more guidance.
Reply #72015-09-18
Small-scale tests in the laboratory should be conducted first before moving to industrial production, so as to avoid future problems
Reply #82015-11-10
Barium carbonate is the best choice, as it contains no additional substances. Barium chloride produces chlorides, and even if it is a purification agent, it still results in chlorides; therefore, using barium chloride is more cost-effective.

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