Preparation method of waterproof iron oxide-based desulfurizer
An iron oxide-based, desulfurizing agent technology, applied in chemical instruments and methods, refining with metal oxides, separation methods, etc., can solve the problems of easy agglomeration, mechanical mixing difficulty, low chemical activity of magnesium sulfate, etc. Easy to mix, easy to put into production immediately, low cost effect
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Embodiment 1
[0012] FeSO 4 ·7H 2 O (content ≥99.0%, AR) 70.0g, NaOH (content ≥96.0%, AR) 20g were dissolved in 30°C distilled water, FeSO 4 The solution was slowly added to the NaOH solution while stirring well. After reacting for 20min, centrifuge to wash SO4 2- , until the filtrate meets Ba 2+ No precipitate formed. Put the precipitate in the air and dry it to 20g~25g, add 1.5g of CaO to the precipitate, mix well, oxidize in the air for 2h, then add 1.8g of MgO, MgCl 2 ·7H 2 O2.6g, NaHCO 3 0.2g is mixed thoroughly to form a precursor. The precursor is extruded into a bar-shaped column with a diameter of 3 mm and a length of 5-8 mm. Put it into an oven, dry at 68°C for 3 hours, turn off the oven, and let it cool down to room temperature naturally to prepare desulfurizer A.
Embodiment 2
[0014] In the precipitate obtained in Example 1, add CaO0.5g, MgO1.8g, MgCl 2 ·7H 2 O2.6g, NaHCO 3 0.2g is mixed thoroughly to form a precursor. The precursor is extruded into a bar-shaped column with a diameter of 3 mm and a length of 5-8 mm. Put it into an oven, dry it at 68°C for 3 hours, turn off the oven, and let it cool down to room temperature naturally to prepare desulfurizer B.
Embodiment 3
[0016] In the precipitate obtained in Example 1, add CaO0.5g, MgO0.9g, MgCl 2 ·7H 2 O1.3g, NaHCO 3 0.2g is mixed thoroughly to form a precursor. The precursor is extruded into a bar-shaped column with a diameter of 3 mm and a length of 5-8 mm. Put it into an oven, dry at 68°C for 3 hours, turn off the oven, and let it cool down to room temperature naturally to prepare desulfurizer C.
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