Immobilized metal porphyrin enzyme catalyst and preparation method thereof
A technology for immobilizing metals and metalloporphyrins, applied in physical/chemical process catalysts, chemical instruments and methods, organic compounds/hydrides/coordination complex catalysts, etc. And strong corrosiveness and other problems, to achieve mild conditions, promote rapid transformation, and strong specificity
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Embodiment 1
[0032] Embodiment 1 This embodiment illustrates the catalyst method of synthetic metalloporphyrinase
[0033] Pyridyl porphyrin compound in CoCl 2 solution with FeCl 2 Coordination reaction to form metalloporphyrinase;
[0034] The ionic liquid with the anion functional group of hydroxyl and the cationic functional group of amino is reacted with mesoporous activated carbon molecular sieve material in toluene solution at 110° C. for 24 hours; the carrier is obtained by filtration. Then use dichloromethane Soxhlet extraction for 20h to filter to obtain the carrier, then put the metalloporphyrinase solution into 0.0125M Tris-HCl buffer solution (50mL, pH7.0), and introduce the surface-modified mesoporous activated carbon molecular sieve material. The mixed solution was stirred at a temperature of 30 °C and a rotation speed of 150 rpm until the sample reached adsorption equilibrium.
Embodiment 2
[0035] Example 2 This example illustrates embedding
[0036] Immerse the immobilized metalloporphyrinase solution in CaCl 2solution and stirred for 1 h, the mixture was injected into 2% w / v sodium alginate solution for aging, and finally the enzyme was encapsulated by calcium alginate gel to obtain immobilized metalloporphyrinase embedded in calcium alginate gel , and then dried for later use.
Embodiment 3
[0037] Example 3 This example illustrates the use of immobilized metalloporphyrinase catalysts to catalyze the oxidation of hydroxymethylfurfural (HMF) to furandicarboxylic acid (FDCA)
[0038] Take 1.0g of hydroxymethylfurfural and 5mL of acetonitrile solution into a 10mL round bottom flask, and stir the solution until the solution is clear, then add 50mg of immobilized metalloporphyrinase catalyst and 70% of TBHP oxidant, and generate at 110°C After 60 hours of reaction, the oxidant and catalyst are recovered for future use. Finally, the reaction conversion rate and product purity were analyzed by VarianProstar high performance liquid chromatography.
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