Preparation and characterization of molecularly imprinted polymers for the selective separation of 2,4-dichlorophenoxyacetic acid
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Abstract
As a method of preparing ligand-selective cavities in a synthetic polymer matrix, molecular imprinting technique has been attracting significant interest from a large number of areas in chemistry and analytical sciences. In this study, molecularly imprinted polymers (MIPs) were prepared with styrene, 4-vinylpyridine (4-VPy), and divinylbenzene (DVB) for the separation of hazardous 2,4-dichlorophenoxyacetic acid (2,4-D), and the selectivity of MIPs as adsorbed 2,4-D and structurally similar materials was evaluated. The template was removed through the swelling process of toluene/ethanol, and the removal ratio was about 95–99%, respectively. MIPs synthesized in this study had good adsorption selectivity in the presence of other materials, although there was a difference of adsorption quantities (uptake) in the functional monomer (4-VPy contents) and the cross-linker (DVB contents). The results exhibit that the selectivity of MIPs was improved significantly by controlling the cross-linker. We expect that molecular imprinting technique will serve as a novel method for selective separation of specific materials in various fields, especially in the fields of environment and pharmaceutics.
Keywords
Benzoic Acid Guest Molecule Functional Monomer Imprint Polymer Selectivity FactorNotes
Acknowledgements
This work was supported by the Korea Research Foundation Grant funded by the Korean Government (MOEHRD) (KRF-2007-412-J02001).
References
- 1.Kempe M, Mosbach K (1995) J Chromatogr A 691:317CrossRefGoogle Scholar
- 2.Sreenivasan K, Sivakumar R (1997) J Appl Polym Sci 66:2539CrossRefGoogle Scholar
- 3.Sreenivasan K (1998) J Appl Polym Sci 70:15CrossRefGoogle Scholar
- 4.Sreenivasan K (2007) J Mater Sci 42:7575. doi: https://doi.org/10.1007/s10853-007-1625-7 CrossRefGoogle Scholar
- 5.Park HR, Yoon SD, Bang EY, Rogers KR, Chough SH (2005) J Appl Polym Sci 96:650CrossRefGoogle Scholar
- 6.Svenson J, Nicholls IA (2001) Anal Chim Acta 435:19CrossRefGoogle Scholar
- 7.Wulff G (1995) Angew Chem Int Ed Engl 34:1812CrossRefGoogle Scholar
- 8.Mosbach K, Mayes AG (1997) Trends in analytical chemistry. Elsevier, AmsterdamGoogle Scholar
- 9.Matsui J, Doblhoff-Dier O, Takeuchi T (1995) Chem Lett 67:4404Google Scholar
- 10.Fisccher L, Muller R, Ekberg B, Mosbach K (1991) J Am Chem Soc 113:9358CrossRefGoogle Scholar
- 11.Vlatakis G, Andersson LI, Muller R, Mosbach K (1993) Nature 361:645CrossRefGoogle Scholar
- 12.Muldoon MT, Stanker LH, Agric J (1995) Food Chem 43:1424CrossRefGoogle Scholar
- 13.Mosbach K, Nicholls IA, Ramstrom O (1992) Swed Pat Appl 9203914Google Scholar
- 14.Bystrom SE, Borje A, Akermark B (1993) J Am Chem Soc 115:2081CrossRefGoogle Scholar
- 15.Yano K, Karube I (1999) Trends Anal Chem 18:199CrossRefGoogle Scholar
- 16.Kriz D, Mosbach K (1995) Anal Chim Acta 300:71CrossRefGoogle Scholar
- 17.Mullett WM, Lai EPC (1998) Anal Chem 70:3636CrossRefGoogle Scholar
- 18.Mullett WM, Dirie MF, Lai EPC, Guo HS, He XW (2000) Anal Chim Acta 414:123CrossRefGoogle Scholar
- 19.Shea KJ (1994) Trends Polym Sci 2:199Google Scholar
- 20.Park HR, Yoon SD, Lee JC, Chough SH (2007) J Appl Polym Sci 105:2824CrossRefGoogle Scholar