The use of chelating agents in affinity chromatography poses significant challenges due to their tendency to form chemical bonds with metals. During the purification process, these agents can dissociate from the matrix, potentially contaminating the purified biomolecule and rendering it unsuitable for therapeutic or other biological applications. This study introduces an innovative approach for the electroadsorption of Cu²⁺ ions onto polyacrylamide (PAam) cryogels using a fixed-bed system under the application of electrical potential. This method reduces the risk of metal contamination by eliminating the need for chelating agents commonly used in immobilized metal ion affinity chromatography (IMAC). The cryogels demonstrated excellent structural integrity, retaining their shape after compression and rehydration. Electroadsorption experiments revealed that a minimum voltage of 3V was required to establish effective removal sites for Cu²⁺ ions, with a maximum removal capacity of approximately 19 mg/g (PAam)". At higher voltages (3V and 5V), the electroadsorbed ions were efficiently desorbed using ethylenediaminetetraacetic acid (EDTA) solution. The distinct d⁹ electron configuration of Cu²⁺ makes it particularly prone to forming coordinated bonds with the lone pairs of N present in the PAam structure. The study also highlights the impact of flow rates on saturation times, with faster rates leading to quicker saturation without compromising removal efficiency. These results demonstrate that electroadsorption in PAam cryogels is a promising alternative to IMAC for metal ion purification in chromatographic applications, providing a cleaner and more cost-effective solution.
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