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Abstracts Book - IMRC 2018

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• SA1-P021<br />

SYNTHESIS OF MESOPOROUS CARBON XEROGELS WITH<br />

CUSTOMIZED POROSITY FOR PROTEIN SEPARATION<br />

Luis Adrián Ramírez Montoya 1 , Ana Arenillas 1 , J. Ángel Menéndez 1 , Miguel Montes Morán 1<br />

1 Instituto Nacional del Carbón (INCAR-CSIC), Procesos químicos en energía y medio ambiente,<br />

Spain.<br />

Protein adsorption on mesoporous materials has been intensively studied and<br />

plenty of technical applications have been envisaged including drug delivery,<br />

biosensing systems, biocatalysis and coating of chemical devices. There have<br />

been many studies of the potential to use mesoporous materials for<br />

biomolecules adsorption and separation. It has been shown that this type of<br />

materials is useful for stable entrapment of biomolecules and the stabilization<br />

of biologically interesting molecules under different conditions. In this sense the<br />

use of mesoporous carbon xerogels are interesting for this purpose since their<br />

properties can be tailored for different proteins and applications. These<br />

materials, obtained after the carbonization under N2 atmosphere in a tubular<br />

furnace a 700 °C of an organic gel product of the polymerization reaction<br />

between resorcinol and formaldehyde in presence of water and methanol<br />

media and using NaOH as catalyst, represent an attractive alternative for use in<br />

protein fractionation. In addition, the use of microwave heating can reduce<br />

drastically the time hence their cost of production. The versatility of these<br />

materials allows producing carbon xerogels with highly controlled porosity with<br />

a narrow pore size distribution in the mesoporous range. In this sense, three<br />

mesoporous carbon xerogels with an average pore size of 15, 30 and 55 nm<br />

were obtained and labelled as CX-15, CX-30 and CX-55 respectively. The<br />

homogeneity and tailored porosity of these carbon xerogels make them<br />

appropriate for application in the separation of complex mixtures of different<br />

biomolecules. Cytochrome C, BSA, Lysozyme and Myoglobin were selected as<br />

model proteins for adsorption and separation tests based on its differences in<br />

molecular size and isoelectric point with a good performance in the separation<br />

of binary mixtures varying the CX used and the experimental conditions in terms<br />

of pH and ionic strength. A selective adsorption of target proteins in these<br />

materials could be achieved through mainly three mechanisms involved: size<br />

exclusion, electrostatic and hydrophobic interactions with the presence of<br />

synergistic and antagonistic effects depending on the protein mixture and<br />

experimental conditions used.

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