Preparation method of molecularly imprinted polymeric microspheres for 2,4,6-trinitrophenol detection
A technology of molecularly imprinted microspheres and trinitrophenol, applied in the field of detection 2
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[0052] A preparation method of molecularly imprinted polymer microspheres for detection of 2,4,6-trinitrophenol, characterized in that: 2,4,6-trinitrophenol and N,N'-diisopropyl The polynitrophenol derivatives generated by the carbodiimide reaction have bright yellow fluorescence, and their fluorescence has open-close characteristics under acid-base conditions. The molecularly imprinted polymer microspheres are eluted in the imprinted layer. Molecules, the inner formation of the imprinting layer has a cavity structure that is complementary to the structure, size and functional group of the imprinted molecule, and the polymer microspheres that elute the imprinted molecule have specific recognition sites for the target analyte molecule. Molecular selective identification and detection, the above-mentioned preparation process includes the following four steps:
[0053] The first step is the synthesis of 2,4,6-trinitrophenol derivatives: Weigh 0.4-0.6 g of the treated 2,4,6-trinit...
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[0058] 2,4,6-Trinitrophenol and N,N'-diisopropylcarbodiimide are produced by nucleophilic addition reaction of polynitrophenol derivatives. After separation and purification, 2,4,6- Molecularly imprinted polymer microspheres were prepared by copolymerization of trinitrophenol derivative PAD1 with functional monomers, cross-linking agents and initiators. After eluting the template molecule PAD1, polymer microspheres with selective recognition and fluorescence signal output for PAD1 were obtained .
[0059] The first step is the synthesis of 2,4,6-trinitrophenol derivatives: Weigh 0.5 g of the treated 2,4,6-trinitrophenol into a 100 mL three-necked flask, and then add 7.5 mL of dichloromethane After ultrasonic dispersion, 0.3 g of N,N'-diisopropylcarbodiimide was added, and the solution immediately turned reddish-brown. It was stirred for 2 h under nitrogen atmosphere. Due to the volatilization of dichloromethane, the solution became viscous. dried in a vacuum drying oven at 40...
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