Yellow inorganic pigment taking bismuth and vanadium as basic adulterants as well as preparation method and application thereof
An inorganic pigment and basic technology, applied in inorganic pigment processing, chemical instruments and methods, fibrous fillers, etc., can solve the problems of dull color, complex bismuth vanadate process, poor tinting strength, etc., and achieve high tinting strength and vividness. And the effect of good gloss and excellent weather resistance
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Embodiment 1
[0043] Embodiment 1 (molybdenum bismuth vanadium)
[0044] 107.7 grams of bismuth nitrate in acetic acid solution (specific gravity 1.607 g / cm 3) into a 5-liter reactor, add hot water to adjust to 0.570 L and adjust the temperature to 70°C. A 3.6 liter solution containing 14.779 grams of sodium vanadate and 18.333 grams of sodium molybdate was added with stirring. The dropwise addition was performed within 2 hours. During this time, the pH of the added reaction mixture gradually rose to 0.5; adjusted to 4.5 by dropwise addition of 63 ml of 50% caustic soda. The water bath was heated to 70° C., and after stirring for 1 h, the pH was stabilized at 3.81 h. Then, the mixture was filtered, washed, and dried at 90° C. for 12 hours to obtain 85.5 g of a precursor. Then, the yellow pigment obtained at 620° C. was ball-milled in a ball mill, filtered, dried and ground to obtain the product.
Embodiment 2
[0045] Embodiment 2 (pure bismuth vanadate)
[0046] A sample of pure bismuth vanadate was prepared according to the method of Example 1, except that sodium molybdate was omitted: to 48.98 grams of bismuth nitrate was added 15.12 sodium metavanadate.
Embodiment 3
[0047] Embodiment 3 (silicon coated bismuth vanadate)
[0048] According to the procedure described in Example 1, silicon coated bismuth vanadate was prepared by mixing 102.240 grams of bismuth nitrate, 28.700 grams of sodium vanadate and 3.750 grams of sodium metasilicate. Tinting power and hiding power are higher than the pure bismuth vanadate of embodiment 2.
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