Preparation method, application and use method of capsaicin molecularly imprinted magnetic beads
A technology of molecular imprinting and capsaicin, applied in chemical instruments and methods, alkali metal compounds, alkali metal oxides/hydroxides, etc., can solve the problems of poor selectivity and low extraction efficiency of capsaicin
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Embodiment 1
[0027] 1. Double bond modification:
[0028] Add 0.1g of ferric oxide and 2mL of NH to 100mL of absolute ethanol solution 3 ·H 2 O and 1mL of γ-methacryloxypropyltrimethoxysilane (MPS), after ultrasonic mixing, heated to reflux for 5h, after the reaction was complete, washed with ethanol, set to 50mL.
[0029] 2. Molecular imprinting polymerization of capsaicin:
[0030] Add 50mL of double-bond-modified ferric oxide, 50mL of ethanol, 0.05g of dihydrocapsaicin, 90mL of toluene, and 50μL of methacrylic acid (MAA) into a three-necked flask, oscillate ultrasonically for 15min, and keep away from light for 12h to form a template-monomer Prepolymer, then add 1.2mL cross-linking agent ethylene glycol dimethacrylate (EGDMA) and 0.2g initiator 2,2 azobisisobutyronitrile (AIBN) successively, and ultrasonically vibrate for 15min at room temperature. Mechanically stir the reaction in a water bath at 65°C for 10 hours. After cooling, remove unreacted functional monomers and template mol...
Embodiment 2
[0039] 1. Double bond modification:
[0040] Add 0.1g of ferric oxide and 2mL of NH to 100mL of absolute ethanol solution 3 ·H 2 O and 1mL oleic acid, after ultrasonic mixing, heated to reflux for 5h, after the reaction was complete, washed with ethanol until no free oleic acid, toluene to 50mL.
[0041] 2. Molecular imprinting polymerization of capsaicin:
[0042] Add 50mL of double-bond modified ferric oxide, 0.1g of natural capsaicin, 90mL of toluene, and 200μL of methacrylic acid (MAA) into the three-necked flask, oscillate ultrasonically for 15min, and keep away from light for 12h to form a template-monomer prepolymer. Then add 1.2mL of cross-linking agent ethylene glycol dimethacrylate (EGDMA) and 0.2g of initiator 2,2-azobisisobutyronitrile (AIBN) successively, ultrasonically shake for 15min at room temperature, and place in a water bath at 65°C Mechanically stirred and reacted for 12 hours, and after cooling, unreacted functional monomers and template molecules were...
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