Potentiometric, Kinetic, and Thermodynamic Investigations into Cu2+ Ion Binding Properties of Vinyl Imidazole Containing IMAC Adsorbent


Cam T., OSMAN B., KARA A., Demirbel E., Besirli N., Irez G.

JOURNAL OF APPLIED POLYMER SCIENCE, cilt.131, sa.2, 2014 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 131 Sayı: 2
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1002/app.39751
  • Dergi Adı: JOURNAL OF APPLIED POLYMER SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: copolymers, crosslinking, functionalization of polymers, METAL-AFFINITY-CHROMATOGRAPHY, HUMAN SERUM-PROTEINS, DEPENDENT INTERACTION CHROMATOGRAPHY, PERFORMANCE LIQUID-CHROMATOGRAPHY, STABILITY-CONSTANTS, POLYELECTROLYTE COMPLEXES, CU(II)-LOADED COPOLYMERS, N-ISOPROPYLACRYLAMIDE, SURFACE DOMAINS, ALPHA-AMYLASE
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

In this study, the use of the potentiometric method for the determination of the protonation constant of vinyl imidazole (VIM) and the stability constant of the Cu2+ ion complex of VIM used in the immobilized metal ion affinity chromatography (IMAC) was investigated. For this purpose, poly(ethylene glycol dimethacrylate-n-vinyl imidazole) [poly(EGDMA-VIM)] microspheres (average diameter 150-200 mu m) were prepared. The microspheres were characterized by elemental analysis, N-2 adsorption/desorption isotherms, elemental analysis, energy dispersive spectroscopy (EDS). Protonation constants of vinyl imidazole and the metal-ligand stability constant of vinyl imidazole with Cu2+ ions have been determined potentiometrically in 0.1M NaCl aqueous solution at 298, 318, and 338 K, respectively. The corresponding thermodynamic parameters of protonation and complexation processes (Delta G, Delta H, and Delta S) were derived and discussed. The formation kinetics of Cu2+-vinyl imidazole complex were also investigated, and the process obeyed the pseudo-second-order kinetic model. (C) 2013 Wiley Periodicals, Inc.