Preparation method of high-purity boric acid
A technology of high-purity boric acid and boric acid, applied in the direction of boron oxyacids, boron oxide compounds, etc., can solve problems such as heat loss, long process flow, complex impurities, etc., reduce production costs, increase mass transfer rate, and simplify the process flow Effect
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Embodiment 1
[0023] At room temperature, dissolve 4g of boric acid in 95.8g of deionized water, then add 0.2g of isopropanol to form 100g of initial circulating mother liquor, put it in a 500ml three-necked flask, then add 30g of industrial boric acid and 0.0006mol of sulfuric acid, stir and heat to 95 ℃, keep warm for 1 hour, stir and cool down to crystallize to room temperature, precipitate wet boric acid crystals, place them in a Buchner funnel, vacuum filter the mother liquor, the mother liquor passes through the cation exchange resin column and the anion exchange resin column in turn, and the obtained clean mother liquor is divided into two Wash the above-mentioned boric acid crystals, and quickly filter out the circulating mother liquor. The drained boric acid is placed in a vacuum drying oven and dried in vacuum at 70° C. for 3 hours to obtain 29 g of granular high-purity boric acid. The circulating mother liquor can be recycled repeatedly.
Embodiment 2
[0025] Add 60g of 95% industrial boric acid to a 1000ml three-necked flask, and 600g of saturated boric acid solution prepared at room temperature as the circulating mother liquor. The circulating mother liquor contains 0.6g of ethanol, then add 0.0012mol of hydrofluoric acid aqueous solution, stir and heat to 80°C, keep warm After 2 hours, stir and cool down to crystallize to room temperature, place the wet boric acid crystals in a Buchner funnel, vacuum filter the mother liquor, pass through the cation exchange resin column and the anion exchange resin column successively, and wash the boric acid crystals twice with the obtained clean mother liquor, The circulating mother liquor was quickly filtered out, and the drained boric acid was placed in a vacuum drying oven, and dried in vacuum at 70° C. for 3 hours to obtain 55 g of granular high-purity boric acid.
Embodiment 3
[0027] Add 60g of industrial boric acid and 300g of the circulating mother liquor obtained from Example 2 into a 500ml three-necked flask, then add 0.001mol of nitric acid, stir and heat to 85°C, keep warm for 2 hours, stop stirring and naturally cool down to room temperature to obtain boric acid crystals, and wet boric acid The crystals are placed in a Buchner funnel, and the vacuum-filtered mother liquor passes through a cation exchange resin column and an anion exchange resin column in turn, and the obtained clean mother liquor washes the boric acid crystals twice, and quickly filters out the circulating mother liquor, and the dried boric acid crystals In a vacuum drying oven, vacuum-dry at 70°C for 3 hours to obtain 60 g of flaky high-purity boric acid, and the circulating mother liquor can be reused repeatedly.
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