Preparing method of porous poly ion liquid catalyst used for synthesizing biodiesel
A technology of polyionic liquid and synthetic biology, applied in the field of catalytic synthesis of biodiesel, can solve problems such as restricting application, and achieve the effects of good reusability, easy separation and recovery, and large comparative area.
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Embodiment 1
[0023] 32mmol of anhydrous iron trichloride, 12.8mmol of trisodium citrate dihydrate, 19.2mmol of anhydrous sodium acetate, and 2560mmol of ethylene glycol were mixed and stirred until completely dissolved. The solution was transferred to a hydrothermal reactor and kept at 180°C for 16h. The product is washed and dried to obtain 2.02g Fe 3 O 4 Particles. 1gFe 3 O 4 Disperse in 40ml absolute ethanol by ultrasonic and add 1ml NH 3 ·H 2 O and 1g of γ-methacryloxypropyltrimethoxysilane were reacted at 30°C for 24h. 1.28g modified magnetic material Fe is obtained after separation, washing and vacuum drying 3 O 4 MPS.
[0024] 1gFe 3 O 4 MPS was dispersed in 40ml of absolute ethanol, and 1g of 1-vinyl-3-propylsulfonic acid imidazole tetrafluoroborate ionic liquid and 0.05g of azobisisobutyronitrile were added. N 2 React at 60°C for 24h in an atmosphere. After product separation, washing and vacuum drying, 1.75g Fe is obtained 3 O 4 PIL. Add hydrochloric acid (8mol / L, 2.5ml) to 50m...
Embodiment 2
[0027] 32mmol of anhydrous iron trichloride, 19.2mmol of trisodium citrate dihydrate, 28.8mmol of anhydrous sodium acetate, and 3200mmol of ethylene glycol were mixed and stirred until completely dissolved, then transferred to a hydrothermal reactor, kept at 220°C for 8 hours. 2.29g Fe after washing and drying 3 O 4 Particles. 1.0gFe 3 O 4 Ultrasonic dispersion in 80ml absolute ethanol, add 2ml NH 3 ·H 2 O and 4.0g γ-methacryloxypropyltrimethoxysilane were reacted at 50°C for 72h. 1.61g of modified magnetic material Fe is obtained after separation, washing and vacuum drying 3 O 4 MPS.
[0028] 1gFe 3 O 4 MPS was dispersed in 50ml of absolute ethanol, and 3g of 1-vinyl-3-propylsulfonic acid imidazole hydrogen sulfate ionic liquid and 0.15g of azobisisobutyronitrile were added. N 2 React at 90°C for 36 hours in an atmosphere. After product separation, washing and vacuum drying, 3.65g Fe is obtained 3 O 4 PIL. Add hydrochloric acid (12mol / L, 5ml) to 50ml ethanol, add 1gFe 3 O 4 P...
Embodiment 3
[0031] 32mmol of anhydrous iron trichloride, 16mmol of trisodium citrate dihydrate, 24mmol of anhydrous sodium acetate, and 2880mmol of ethylene glycol were mixed and stirred until completely dissolved, then transferred to a hydrothermal reaction vessel, kept at 200°C for 12h. 2.15g Fe after washing and drying 3 O 4 Particles. 1gFe 3 O 4 Ultrasonic dispersion in 60ml absolute ethanol, add 2ml NH 3 ·H 2 O and 2.5g of γ-methacryloxypropyltrimethoxysilane were reacted at 40°C for 48h. 1.45g modified magnetic material Fe is obtained after separation, washing and vacuum drying 3 O 4 MPS.
[0032] 1gFe 3 O 4 MPS was dispersed in 40 ml of absolute ethanol, and 3 g of 1-vinyl-3-butanesulfonic acid imidazole hydrogen phosphate ionic liquid and 0.1 g of azobisisobutyronitrile were added. N 2 React at 75°C for 30h in an atmosphere. After product separation, washing and vacuum drying, 3.42g Fe is obtained 3 O 4 PIL. Add hydrochloric acid (10mol / L, 4ml) to 80ml ethanol, add 0.8g Fe 3 O 4 P...
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