Method for preparing hydrophobic white carbon black
A technology of hydrophobic silica and precipitation silica, applied in the direction of fibrous fillers, dyed low-molecular-weight organic compounds, etc., can solve the problems of increased modification cost, complicated modification process, environmental pollution, etc., and achieves clean solvent free. The effect of pollution, simple operation process and improved hydrophobicity
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Embodiment 1
[0028] Accurately weigh 0.09g of cetyltrimethylammonium bromide (CTAB) and dissolve it in 90mL of deionized water to obtain a modifier solution, then add 6g of precipitated white carbon black to the above modifier solution to adjust the pH value of the system 8. Stir magnetically in a constant temperature water bath at 50°C for 30 minutes at a speed of 350 rpm. After filtration and drying, hydrophobic silica is obtained. The activation degree is 99.21%.
Embodiment 2
[0030] Accurately weigh 0.18g of cetyltrimethylammonium chloride (CTAC) and dissolve it in 100mL of deionized water to obtain a modifier solution, then add 9g of precipitated white carbon black to the above modifier solution to adjust the pH value of the system 8, magnetically stirred in a constant temperature water bath at 60°C for 40 minutes at a speed of 300 rpm, filtered and dried to obtain hydrophobic silica, and its activation degree was detected to be 99.80%.
Embodiment 3
[0032] Accurately weigh 0.75g of dodecyltrimethylammonium chloride (DTAC) and dissolve it in 135mL of deionized water to obtain a modifier solution, then add 15g of precipitated white carbon black to the above modifier solution to adjust the pH value of the system 8. Stir magnetically in a constant temperature water bath at 75°C for 70 minutes at a speed of 450 rpm. After filtration and drying, hydrophobic silica is obtained. The activation degree is 98.78%.
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