4.7 Article

Dissolution of Silk Fibroin in Mixtures of Ionic Liquids and Dimethyl Sulfoxide: On the Relative Importance of Temperature and Binary Solvent Composition

Journal

POLYMERS
Volume 14, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/polym14010013

Keywords

silk fibroin dissolution; effects of temperature; ionic liquid molecular structure; design of experiments; molecular dynamics simulations

Funding

  1. FAPESP (Fundacao de Amparo a pesquisa do estado de Sao Paulo) [2014/22136-4]
  2. CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico) [306108/2019-4]
  3. FAPESP [2016/22869-7]

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The dependence of silk fibroin dissolution in mixtures of DMSO with ionic liquids on temperature and DMSO mole fraction was studied. Design of experiments was used to determine the relationship between mass fraction of dissolved silk fibroin and temperature and DMSO mole fraction. The results showed that different ionic liquids have different effects on silk fibroin dissolution.
We studied the dependence of dissolution of silk fibroin (SF) in mixtures of DMSO with ionic liquids (ILs) on the temperature (T = 40 to 80 degrees C) and DMSO mole fraction (chi(DMSO) = 0.5 to 0.9). The ILs included BuMeImAcO, C(3)OMeImAcO, AlBzMe(2)NAcO, and Bu4NAcO; see the names and structures below. We used design of experiments (DOE) to determine the dependence of mass fraction of dissolved SF (SF-m%) on T and chi(DMSO). We successfully employed a second-order polynomial to fit the biopolymer dissolution data. The resulting regression coefficients showed that the dissolution of SF in BuMeImAcO-DMSO and C(3)OMeImAcO-DMSO is more sensitive to variation of T than of chi(DMSO); the inverse is observed for the quaternary ammonium ILs. Using BuMeImAcO, AlBzMe(2)NAcO, and molecular dynamics simulations, we attribute the difference in IL efficiency to stronger SF-IL hydrogen bonding with the former IL, which is coupled with the difference in the molecular volumes and the rigidity of the phenyl ring of the latter IL. The order of SF dissolution is BuMeImAcO-DMSO > C(3)OMeImAcO-DMSO; this was attributed to the formation of intramolecular H-bonding between the ether oxygen in the side chain of the latter IL and the relatively acidic hydrogens of the imidazolium cation. Using DOE, we were able to predict values of SF-m%; this is satisfactory and important because it results in economy of labor, time, and material.

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