Dissolution of microcrystalline cellulose (MCC) in pure ionic liquids (ILs) and IL/dimethyl sulfoxide (DMSO) mixtures (mole fraction χDMSO = 0.2–0.9) was quantified using a specially constructed mechanical stirring system that allows reproducible agitation speed; temperature control, and minimum solution-air contact. The electrolytes employed were: 1-(n-butyl)-3-methylimidazolium acetate (C4MeIm AcO), 1-(methoxyethyl)-3-methylimidazolium acetate (C3OMeIm AcO), 1,8-diazabicyclo[5.4.0]undec-7-enium acetate (DBU AcO), tetramethylguanidinium acetate (TMG AcO), and tetra(n-butyl)ammonium fluoride hydrate (TBAF·xH2O). The effects on MCC dissolution of IL/DMSO composition, and temperature (50, 70°C) were studied. C4MeIm AcO and C4MeIm AcO/DMSO were more efficient solvents than their C3OMeIm AcO counterparts, due to “deactivation” of the ether oxygen of C3OMeIm AcO. MCC dissolution by C4MeIm AcO/DMSO was compared with DBU AcO/DMSO, TMG AcO/DMSO at χDMSO = 0.6, and TBAF·xH2O/DMSO at χDMSO = 0.95. The relative efficiency was (solutions in DMSO): C4MeIm AcO > C3OMeIm AcO > DBU AcO > TMG AcO > TBAF·xH2O. The efficiency of C4MeIm AcO relative to C3OMeIm AcO is due to higher solution basicity. Isothermal titration calorimetry was used to study cellobiose-solvent interactions. Except for TBAF·xH2O/DMSO, these interactions are exothermic; the relative solvent efficiency increases with increasing dissolution |enthalpy|. Using the mole fraction concentration scale to report cellulose dissolution avoids possible ambiguities.
The physical dissolution of carbohydrates (cellulose, chitin, and starch), i.e., without formation of covalent bonds requires that the solvent possess certain physicochemical properties. Concentrating on cellulose, the solvent should act...
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 °C) and DMSO mole fraction (χDMSO = 0.5 to 0.9). The ILs included BuMeImAcO, C3OMeImAcO, AlBzMe2NAcO, 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 χDMSO. 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 C3OMeImAcO-DMSO is more sensitive to variation of T than of χDMSO; the inverse is observed for the quaternary ammonium ILs. Using BuMeImAcO, AlBzMe2NAcO, 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 > C3OMeImAcO-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.
We studied the dissolution of microcrystalline cellulose (MCC) in binary mixtures of dimethyl sulfoxide (DMSO) and the ionic liquids: allylbenzyldimethylammonium acetate; 1-(2-methoxyethyl)-3-methylimidazolium acetate; 1,8-diazabicyclo [5.4.0]undec-7-ene-8-ium acetate; tetramethylguanidinium acetate. Using chemometrics, we determined the dependence of the mass fraction (in %) of dissolved cellulose (MCC-m%) on the temperature, T = 40, 60, and 80 °C, and the mole fraction of DMSO, χDMSO = 0.4, 0.6, and 0.8. We derived equations that quantified the dependence of MCC-m% on T and χDMSO. Cellulose dissolution increased as a function of increasing both variables; the contribution of χDMSO was larger than that of T in some cases. Solvent empirical polarity was qualitatively employed to rationalize the cellulose dissolution efficiency of the solvent. Using the solvatochromic probe 2,6-dichloro-4-(2,4,6-triphenylpyridinium-1-yl)phenolate (WB), we calculated the empirical polarity ET(WB) of cellobiose (a model for MCC) in ionic liquid (IL)–DMSO mixtures. The ET(WB) correlated perfectly with T (fixed χDMSO) and with χDMSO (fixed T). These results show that there is ground for using medium empirical polarity to assess cellulose dissolution efficiency. We calculated values of MCC-m% under conditions other than those employed to generate the statistical model and determined the corresponding MCC-m% experimentally. The excellent agreement between both values shows the robustness of the statistical model and the usefulness of our approach to predict cellulose dissolution, thus saving time, labor, and material.
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