Please submit manuscripts on new website https://asianpubs.org/index.php/ajchem
Crossref Similarity Check logo Crossref logo Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

Preparation of Molecularly Imprinted Polymer and Its Recognition Property for Acetanilide

Shunli Fan*, Yaqun Cheng, Ruxin Luo and Jing'e Huo

Henan Normal University, Henan Key Laboratory for Environmental Pollution Control, Key Laboratory for Yellow River and Huai River Water Environmental and Pollution Control, Ministry of Education, Xinxiang 453007, Henan Province, P.R. China

*Corresponding author: Tel: +86 373 3325310; E-mail: shunlifan@163.com
Abstract

Molecularly imprinted polymers with highly selective recognition for acetanilide were prepared by precipitation polymerization using acetanilide as template molecule, methacrylic acid as functional monomer and ethylene glycol dimethaerylate as crosslinker. The experiment measured the influence of the molar ratio of the template molecule and the functional monomer upon the adsorption capacity of the polymers and the optimized ratio was obtained to be n(acetanilide) : n(methacrylic acid) = 1:4. Scatchard analysis indicated the imprinted polymer acetanilide template molecule and functional monomer methacrylic acid formed one kind of binding site, binding site dissociation constant KD = 4.35 mmol/L, the apparent maximum binding capacity Qmax = 111.87 μmol/g.
Keywords

Acetanilide, Molecularly imprintied polymer, Adsorption property, Spectrometric detection.
Reference (14)

1.      Q.H. Zhu, J.F. He and J.Y. Feng, J. Eur. Polym., 43, 4043 (2007); doi:10.1016/j.eurpolymj.2007.06.036.

2.      B. Okutucu and S. Önal, Talanta, 87, 74 (2011); doi:10.1016/j.talanta.2011.09.043.

3.      C.-Y. Chen, C.-H. Wang and A.-H. Chen, Talanta, 84, 1038 (2011); doi:10.1016/j.talanta.2011.03.009.

4.      K. Yongfeng, D. Wuping, L. Yan, K. Junxia and X. Jing, Carbohydr. Polym., 88, 459 (2012); doi:10.1016/j.carbpol.2011.12.027.

5.      W.C. Zhang, H.T. Zhang, Q. Zhang, Y.F. Cui, Z.Y. Wu, R.J. Zheng and L. Liu, Sep. Purif. Technol., 81, 411 (2011); doi:10.1016/j.seppur.2011.08.012.

6.      M. Tian, H. Zhang and K.H. Row, Asian J. Chem., 24, 4606 (2012).

7.      Y. Mao, Y. Bao, S.Y. Gan, F.H. Li and L. Niu, Biosens. Bioelectron., 28, 291 (2011); doi:10.1016/j.bios.2011.07.034.

8.      Y. Xiong, H.J. Zhou, Z.J. Zhang, D.Y. He and C. He, Spectrochim. Acta A, 66, 341 (2007); doi:10.1016/j.saa.2006.03.001.

9.      M.B. Gholivand and N. Karimian, Mater. Sci. Eng. C, 31, 1844 (2011); doi:10.1016/j.msec.2011.08.019.

10.  K. Rostamizadeh, M. Vahedpour and S. Bozorgi, Int. J. Pharm., 424, 67 (2012); doi:10.1016/j.ijpharm.2011.12.054.

11.  N. Denderz, J. Lehotay, J. Cizmárik, Z. Cibulková and P. Šimon, J. Chromatogr. A, 1235, 77 (2012); doi:10.1016/j.chroma.2012.02.051.

12.  V. Abbate, A.R. Bassindale, K.F. Brandstadt and P.G. Taylor, J. Catal., 284, 68 (2011), J. Catal., 284, 68 (2011); doi:10.1016/j.jcat.2011.08.019.

13.  C. Liu, M. Turghun, H. Nurmement, V.P. Elena and H.H. Zeng, Chinese J. Anal. Chem., 38, 1652 (2010).

14.  L.J. Schwarz, B. Danylec, S.J. Harris, R.I. Boysen and M.T.W. Hearn, J. Chromatogr. A, 1218, 2189 (2011); doi:10.1016/j.chroma.2011.02.043.
   View Article PDF File Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.