Prime pigment and its preparation method
A technology of base pigments and metal compounds, applied in inorganic pigment processing, chemical instruments and methods, powder coatings, etc., can solve problems such as low adhesion and easy peeling
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example 1
[0070] Heat 2 liters of deionized water to 85°C under stirring, aiming at maintaining the pH of the solution at 9.0, simultaneously add 1480g of magnesium sulfate aqueous solution (0.45mol / l, MgSO 4 ·7H 2 O) and 32% by weight of sodium oxyoxide in water. After addition of these aqueous solutions, the suspension was filtered, washed with deionized water, and dried at 110°C. The resulting powder was observed using SEM photography to confirm that it was substantially composed of spherical particles with a structure of merged or intersecting leaflets and a particle size of 8 to 17 μm. X-ray diffraction analysis also confirmed that the powder was Mg(OH) 2 .
example 2
[0072] Heat 2 liters of deionized water to 75°C under stirring, aiming to maintain the pH of the solution at 9.0, and simultaneously add 1480g of magnesium sulfate aqueous solution (0.45mol / l, MgSO 4 ·7H 2 O) and 32% by weight aqueous sodium hydroxide solution. After addition of these aqueous solutions, the suspension was filtered, washed with deionized water, and dried at 110°C. The resulting powder was observed by SEM photography to confirm that it was substantially composed of spherical particles with a structure of merged or intersecting leaflets and a particle size of 7 to 10 μm. X-ray diffraction analysis also confirmed that the powder was Mg(OH) 2 .
example 3
[0074] Heat 2 liters of deionized water to 85°C under stirring, aiming at maintaining the pH of the solution at 9.0, simultaneously add 1350 g of water, 28.4 g of sodium sulfate and 150 g of magnesium sulfate (MgSO 4 ·7H 2 O) 1510 g of aqueous solution consisting of 32% by weight aqueous sodium hydroxide solution. After addition of these aqueous solutions, the suspension was filtered, washed with deionized water, and dried at 110°C. The obtained powder was observed by SEM photography to confirm that it was substantially composed of spherical particles with a structure of merged or intersecting leaflet-like flakes and a particle size of 5 to 30 μm. X-ray diffraction analysis also confirmed that the powder was Mg(OH) 2 .
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