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磺胺二甲嘧啶分子印迹聚合物制备与光谱特性

磺胺二甲嘧啶分子印迹聚合物制备与光谱特性

磺胺二甲嘧啶分子印迹聚合物制备与光谱特性

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Preparation and Spectral Characteristic of Molecularly Imprinted<br />

Polymers for Sulfamethazine<br />

L IU Hui2jun 1 , XU Wei2jian 2 , L IU Yao2chi 1 , XION G Yuan2qin 2<br />

1. College of Chemistry and Chemical Engineering , University of South China , Hengyang 421001 , China<br />

2. College of Chemistry and Chemical Engineering , Hunan University , Changsha 410082 , China<br />

Abstract Molecularly imprinted polymers (MIPs) were synthesized , which was initiated by UV photo2induction at low tempera2<br />

ture , with sulfamethazine (SM2 ) was used as template , methacrylic acid (MAA) as monomer , and ethylene glycol dimethylacry2<br />

late ( EGDMA) as crosslinker. By UV spectrometry the authors compared the combination action on sulfamethazine with MAA<br />

and researched the static adsorption ability and selective recognition of the molecularly imprinted polymers. The results showed<br />

that the combination action of functional monomer with template molecules was produced , sulfamethazine imprinted polymers u2<br />

sing methacrylic acid as monomer had higher affinity capability than NMIP and comparatively similar structure substrate of sul2<br />

fisoxazole (SIZ) , while SM2 imprinted polymers could specifically recognize the corresponding imprinted molecules. The static<br />

adsorption modulus of SM2 imprinted polymer was 2821 3 mg mL - 1 and the separate factor was 31 9. Then , the prediction im2<br />

printing principle of sulfamethazine template polymer was given. The infrared spectra of methacrylic acid (MAA) and ethylene<br />

glycol dimethylacrylate ( EGDMA) and MIPs of SM2 were analysed. It was found that the absorbability peak of C C function<br />

group in the IMPs turned out to be very low , but the function group of carboxylic acid in the IMPs did not markedly change. The<br />

results showed that there were some functional groups in MIPs which could interact with the template.<br />

Keywords Sulfamethazine ; Molecularly imprinted polymers ; Spectrum analysis ; Molecular recognition<br />

(Received May 10 , 2006 ; accepted Aug. 20 , 2006)

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