Preparation method of hydroxylated graphene oxide-magnesium titanate/silver molybdate composite material
A composite material, magnesium titanate technology, which is applied in the field of preparation of hydroxylated graphene oxide-magnesium titanate/silver molybdate composite materials, can solve the problems of low processing efficiency, limited adsorption capacity, and difficult repair of composite pollution. Achieve strong adsorption, simple operation, and efficient treatment
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Embodiment 1
[0021] The preparation method of hydroxylated graphene oxide-magnesium titanate / silver molybdate composite material comprises the following steps:
[0022] Step 1: Preparation of Hydroxylated Graphene Oxide
[0023] (1) First, 2.0g graphene oxide, 1.0gP 2 o 5 , 1.0g Na 2 S 2 o 8 and 10 mL concentrated H 2 SO 4 After mixing evenly, heat to 85°C in a water bath, react for 8 hours, and place it for 12 hours after cooling. Repeatedly wash with ultrapure water to remove residual acid, ultrasonicate at 60°C for 5h, then vacuum dry at 65°C, add the dried crystals to 120mL of concentrated H 2 SO 4 , then add 2.0gKNO 3 , and vibrate in the oscillator for 5h, then add 0.5L water, control the temperature at 85°C to react, continue to shake for 3h, wash repeatedly with hydrochloric acid (mass percentage concentration 5-20%) and ultrapure water, and then ultrasonicate at 50°C 5h, obtain the graphene oxide that concentration is 5g / L after constant volume;
[0024] (2) Take 2g of ...
Embodiment 2
[0034] Step 1: Preparation of Hydroxylated Graphene Oxide
[0035] (1) First, 3.0g graphene oxide, 1.5gP 2 o 5 , 1.5gNa 2 S 2 o 8 and 10 mL concentrated H 2 SO 4 After mixing evenly, heat to 95°C in a water bath, react for 10 hours, and place it for 12 hours after cooling. Repeatedly wash with ultrapure water to remove residual acid, ultrasonicate at 80°C for 8h, and then vacuum-dry at 85°C, add the dried crystals to 200mL of concentrated H 2 SO 4 , then add 3.5gKNO 3 , and shake in the oscillator for 10h, then add 1.0L water, control the temperature at 95°C to react, continue to shake for 8h, wash repeatedly with hydrochloric acid (mass percentage concentration 5-20%) and ultrapure water, and then ultrasonic at 80°C 8h, obtain the graphene oxide that concentration is 10g / L after constant volume;
[0036] (2) The bromoethane that takes 5g is dissolved in the volume concentration of 50mL and is 1:1 ammoniacal liquor, after dissolving, add in the graphene oxide gained ...
Embodiment 3
[0046] Step 1: Preparation of Hydroxylated Graphene Oxide
[0047] (1) First, 4.0g graphene oxide, 2.0gP 2 o 5 , 2.0g Na 2 S 2 o 8 and 15 mL concentrated H 2 SO 4 After mixing evenly, heat to 95°C in a water bath, react for 12 hours, and place it for 12 hours after cooling. Repeatedly wash with ultrapure water to remove residual acid, ultrasonicate at 80°C for 8h, and then vacuum-dry at 85°C, add the dried crystals to 200mL of concentrated H 2 SO 4 , then add 3.5gKNO 3 , and shake in the oscillator for 10h, then add 1.0L water, control the temperature at 95°C to react, continue to shake for 10h, wash repeatedly with hydrochloric acid (mass percentage concentration 5-20%) and ultrapure water, and then ultrasonic at 80°C 5 to 8 hours, after constant volume, graphene oxide with a concentration of 10g / L was obtained;
[0048] (2) The bromoethane that takes 5g is dissolved in the volume concentration of 50mL and is 1:1 ammoniacal liquor, after dissolving, add in the graph...
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