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In the name of GOD. Molecular imprinted polymer (MIP). Supervisor Dr. Parchehbaf Presenter Meysam abdi 1391/09/15 2012/12/05. Content. Introduction History Principles Advantage Application Conclusion. Introduction. Base of the method, is recording of target molecule structure
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Molecular imprinted polymer(MIP) Supervisor Dr. Parchehbaf Presenter Meysamabdi 1391/09/15 2012/12/05
Content • Introduction • History • Principles • Advantage • Application • Conclusion
Introduction Base of the method, is recording of target molecule structure In Polymer memory at polymerization process. so that the identification, synthesized polymer only detects the target molecule.
History • 1894, Fischer lock & key theory. • 1930, Polyakov, molecular imprinting in silica’s matrix • 1949, Linuspauling theory, change of antibody structures • 1977, Gunter wulff, molecular imprinting by using covalence banding • 1981, Klaus mosbach, molecular imprinting by using non-covalence banding • 1995, Witcombe, molecular imprinting by using semi-covalence (hybrid) banding www.wikipedia.com www.sciencedirect.com
Research procedure C. Alexander, L. Davidson, and W. Hayes, Tetrahedron 59, 2025-2057 (2003).
Principles www.biotage.com
Fischer Lock & Key theory bonding Remove template molecule PowerPoint of J.jafari thesis Monomer & cross linker Template molecule
Advantage • high selectivity • high pre-Concentration factor • the sorbent is reusable for many times
Sensor Development of a voltammetric sensor based on a molecularly imprinted polymer(MIP) for caffeine measurement Step1:A caffeine-selective molecularly imprinted polymer (MIP) and a non-imprinted polymer (NIP) synthesized. Step2: The MIP, embedded in the carbon paste electrode. Step3:The prepared electrode was used for caffeine measurement via: 1.analyte extraction in the electrode 2.electrode washing 3.electrochemical measurement of caffeine. Step4: DPV were used for determination. A linear range of calibration curve: 6×10-8 to 2.5×10-5 mol/L The detection limit: 1.5×10-8 mol/L. T. Alizadeh et al. / Electrochimica Acta 55 (2010) 1568–1574
A novel high selective and sensitive para-nitrophenol volta- -mmetric sensor, based on a MIP-CP electrode Step1: Para-nitrophenol selective MIP and a non-imprinted polymer (NIP) synthesized Step2:used for carbon paste (CP) electrode preparation. Step3:A dynamic linear range of 8×10-9 to 5×10-6 mol /L was obtained. The detection limit of the sensor was calculated as 3×10-9 mol/L. T. Alizadeh et al. / Talanta 79 (2009) 1197–1203
Application of an Hg2+ selective imprinted polymer for the preparation of a novel highly selective and sensitive electrochemical sensor for the determination of ultra trace Hg2+ Step1: Mercury ion selective cavities were created in the vinyl pyridine based cross-linked polymer. Step2: The interference of different ionic species with the response of the electrode was also studied. Step3: This sensor showed a linear response range of 2.5×10-9 to 5.0×10-7 M and lower detection limit of 5.2×10−10 M (S/N). T. Alizadeh et al. / AnalyticaChimicaActa689 (2011) 52–59
Preparation of nano-sized Pb2+ imprinted polymer and its application as the chemical interface of an electrochemical sensor for toxic lead determination indifferent real samples Step1: a new nano-structured ion imprinted polymer (IIP) was synthesized by copolymerization Step2: A carbon paste electrode modified with IIP-nanoparticles was used for fabrication of a Pb2+ sensitive electrode. Step3: Differential pulse stripping voltammetry method was applied as the determination technique, Step4: The introduced sensor showed a linear range of 1.0×10-9 to 8.1×10-7 M and detection limit of 6.0×10-10 (S/N = 3). T. Alizadeh, S. Amjadi / Journal of Hazardous Materials 190 (2011) 451–459
Determination of Pb2+ in real samples by proposed sensor T. Alizadeh et al. / Talanta 79 (2009) 1197–1203
Prepared electrode T. Alizadeh et al. / Talanta 79 (2009) 1197–1203
Conclusion a new electrochemical sensor for determination of compounds at trace levels was introduced. Application of polymer as a novel modifying agent in the carbon paste electrode made it very selective for compounds determination in the presence of common potential interfering agents. The polymer, used in the carbon paste composition, acted as the selective chemical interface of the sensor as well as a pre-concentration agent.
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