A kind of method for surface modification of magnesium hydroxide flame retardant
A magnesium hydroxide and surface modification technology, which is applied in dyeing polymer organic compound treatment, dyeing physical treatment, fibrous filler, etc., can solve the problems of high cost and cumbersome modification process, and achieve stable structure and remarkable technological progress , Improve the effect of economic and social benefits
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Embodiment 1
[0011] (1) Add 30.00gMg(OH) 2 Place in a beaker and place in 10mL deionized water for ultrasonic dispersion for 15min.
[0012] (2) Add 0.30g sodium lignosulfonate to it respectively, continue ultrasonic dispersion for 10min and then vacuum dry.
[0013] (3) Heat the dried mixture to 100°C in an internal mixer, and banbury at a constant temperature for 0.5 hours.
[0014] (4) Finally, cool to room temperature, centrifuge at 4000r / min for 5min, and vacuum-dry at 80°C for 24h after washing several times, grind and sieve through an 80-mesh standard sieve.
[0015] The contact angle test data of this sample decreased from 88.94 before modification to 45.50.
Embodiment 2
[0017] (1) Add 30.00gMg(OH) 2 Place in a beaker and place in 10mL deionized water for ultrasonic dispersion for 15min.
[0018] (2) Add 0.75g sodium lignosulfonate to it respectively, continue ultrasonic dispersion for 20min and then vacuum dry.
[0019] (3) Heat the dried mixture to 120°C in an internal mixer, and banbury at constant temperature for 1 hour.
[0020] (4) Finally, cool to room temperature, centrifuge at 4000r / min for 5min, and vacuum-dry at 80°C for 24h after washing several times, grind and sieve through an 80-mesh standard sieve.
[0021] The contact angle test data of this sample decreased from 88.94 before modification to 32.42.
Embodiment 3
[0023] (1) Add 30.00gMg(OH) 2 Place in a beaker and place in 10mL deionized water for ultrasonic dispersion for 15min.
[0024] (2) Add 1.5g potassium lignosulfonate to it respectively, continue ultrasonic dispersion for 30min and then vacuum dry.
[0025] (3) Heat the dried mixture to 140°C in an internal mixer, and banbury at constant temperature for 1.5 hours.
[0026] (4) Finally, cool to room temperature, centrifuge at 4000r / min for 5min, and vacuum-dry at 80°C for 24h after washing several times, grind and sieve through an 80-mesh standard sieve.
[0027] The contact angle test data of the sample decreased from 88.94 to 25.44 before modification, which obviously improved its lipophilicity.
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