Lauri K. J. Hauru

Role of Solvent Parameters in the Regeneration of Cellulose from Ionic Liquid Solutions

The ionic liquids 1-ethyl-3-methylimidazolium acetate [emim]OAc, N,N,N,N-tetramethylguanidium propionate [TMGH]EtCO(2), and N,N,N,N-tetramethylguanidium acetate [TMGH]OAc, and the traditional cellulose solvent N-methylmorpholine N-oxide NMMO were characterized for their Kamlet-Taft (KT) values at several water contents and temperatures. For the ionic liquids and NMMO, thresholds of regeneration of cellulose solutions by water were determined using nephelometry and rheometry. Regeneration from wet IL was found to be asymmetric compared to dissolution into wet IL. KT parameters were found to remain almost constant at temperatures, between 20-100 °C, even at different water contents. Among the KT parameters, the β value was found to change most drastically, with an almost linear decrease upon addition of water. The ability of the mixtures to dissolve cellulose was best explained by the difference β-α (net basicity), rather than β alone. Regeneration of cellulose starts at thresholds values of approximately β < 0.8 (β-α < 0.35) and displayed four phases.

Predicting Cellulose Solvating Capabilities of Acid-Base Conjugate Ionic Liquids

Different acid-base conjugates were made by combining a range of bases and superbases with acetic and propionic acid. Only the combinations that contained superbases were capable of dissolving cellulose. Proton affinities were calculated for the bases. A range, within which cellulose dissolution occurred, when combined with acetic or propionic acid, was defined for further use. This was above a proton affinity value of about 240 kcal mol(-1) at the MP2/6-311+G(d,p)//MP2/ 6-311+G(d,p) ab initio level. Understanding dissolution allowed us to determine that cation acidity contributed considerably to the ability of ionic liquids to dissolve cellulose and not just the basicity of the anion. By XRD analyses of suitable crystals, hydrogen bonding interactions between anion and cation were found to be the dominant interactions in the crystalline state. From determination of viscosities of these conjugates over a temperature range, certain structures were found to have as low a viscosity as 1-ethyl-3-methylimidazolium acetate, which was reflected in their high rate of cellulose dissolution but not necessarily the quantitative solubility of cellulose in those ionic liquids. 1,5-Diazabicyclo[4.3.0]non-5-enium propionate, which is one of the best structures for cellulose dissolution, was then distilled using laboratory equipment to demonstrate its recyclability.

Relative and inherent reactivities of imidazolium-based ionic liquids: the implications for lignocellulose processing applications

Novel methods for the fractionation of wood, as a major renewable chemical and material feedstock, are in demand. Ionic liquids, such as 1-ethyl-3-methylimidazolium acetate ([emim][OAc]), are promoted as potential media for these processes. However, the chemical stabilities of such ionic liquids are in question as they may have an effect on process sustainability or efficiency. With anion nucleophilicity and basicity being implicated more in ionic liquid reactivity, a rough scale of the relative reactivities for [emim]-based ionic liquids is demonstrated, based upon their TGA decomposition temperatures. These values are compared to the proton affinities for the anions of those ionic liquids, as a crude measure of nucleophilicity or basicity. The implications for the temperature-dependent chemical stability of imidazolium-based ionic liquids are discussed, in regard to their interactions with wood biopolymers. It is observed that for ionic liquids with less diffuse anions (more nucleophilic or basic), such as [emim][OAc], they unfortunately become more unstable. This is exhibited by a decrease in the thermal stability and an increase in the degree of interaction with the biomass, to the point of better solvation and even covalent interactions with dissolved components. The ab initio proton affinities, dipole moments, van der Waals surface area, and volumes, are presented for an extended series of anions, commonly used in ionic liquids.

Enhancement of ionic liquid-aided fractionation of birchwood. Part 1: autohydrolysis pretreatment

Ionic liquid-cosolvent systems have been proposed as selective solvent media for lignocellulosic materials. We present the ionic liquid-aided fractionation of silver birch (Betula pendula) combined with an autohydrolysis pretreatment. Contrary to untreated birchwood meal, autohydrolyzed birchwood meal reveals quantitative dissolution in 1-ethyl-3-methylimidazolium acetate and distinct separation into the individual wood polymers upon regeneration in acetone/water. The process yields two main fractions, a cellulose-rich precipitate with a residual lignin content of 13–15% and another virtually pure lignin fraction. No cellulose yield loss is observed during the ionic liquid processing step. A comprehensive mass balance of the process, including insoluble material, wash waters, and soluble residues, is provided. The product fractions are characterised for their chemical compositions, molar mass distributions and structural characteristics by Klason lignin and sugar analysis, 13C NMR, GPC and WAXS. The study investigates the effects of wood particle size and autohydrolysis intensity on fractionation efficiency and selectivity.

High‐Strength Composite Fibers from Cellulose–Lignin Blends Regenerated from Ionic Liquid Solution

Composite fibres that contain cellulose and lignin were produced from ionic liquid solutions by dry-jet wet spinning. Eucalyptus dissolving pulp and organosolv/kraft lignin blends in different ratios were dissolved in the ionic liquid 1,5-diazabicyclo[4.3.0]non-5-enium acetate to prepare a spinning dope from which composite fibres were spun successfully. The composite fibres had a high strength with slightly decreasing values for fibres with an increasing share of lignin, which is because of the reduction in crystallinity. The total orientation of composite fibres and SEM images show morphological changes caused by the presence of lignin. The hydrophobic contribution of lignin reduced the vapour adsorption in the fibre. Thermogravimetric analysis curves of the composite fibres reveal the positive effect of the lignin on the carbonisation yield. Finally, the composite fibre was found to be a potential raw material for textile manufacturing and as a precursor for carbon fibre production.

Ionic Liquids for the Production of Man-Made Cellulosic Fibers: Opportunities and Challenges

The constant worldwide increase in consumption of goods will also affect the textile market. The demand for cellulosic textile fibers is predicted to increase at such a rate that by 2030 there will be a considerable shortage, estimated at ~15 million tons annually. Currently, man-made cellulosic fibers are produced commercially via the viscose and Lyocell™ processes. Ionic liquids (ILs) have been proposed as alternative solvents to circumvent certain problems associated with these existing processes. We first provide a comprehensive review of the progress in fiber spinning based on ILs over the last decade. A summary of the reports on the preparation of pure cellulosic and composite fibers is complemented by an overview of the rheological characteristics and thermal degradation of cellulose–IL solutions. In the second part, we present a non-imidazolium-based ionic liquid, 1,5-diazabicyclo[4.3.0]non-5-enium acetate, as an excellent solvent for cellulose fiber spinning. The use of moderate process temperatures in this process avoids the otherwise extensive cellulose degradation. The structural and morphological properties of the spun fibers are described, as determined by WAXS, birefringence, and SEM measurements. Mechanical properties are also reported. Further, the suitability of the spun fibers to produce yarns for various textile applications is discussed.

Dimethyl phosphorothioate and phosphoroselenoate ionic liquids as solvent media for cellulosic materials

A series of novel ionic liquids comprising two asymmetric phosphate-derived anions, namely dimethyl phosphorothioate and dimethyl phosphoroselenoate, and several imidazolium and non-imidazolium-based cations was prepared via a facile synthetic route. Thermal degradation was studied by dynamic thermogravimetric analysis (TGA) revealing a slightly higher stability of the imidazolium ionic liquids and an overall low thermal stability for the phosphoroselenoate salts. Long-term moisture sorption analysis showed correlation with the polarity of the cation and differences in absorption and desorption kinetics. Finally, a Eucalyptus globulus kraft paper grade pulp was dissolved and subsequently regenerated to assess the degradation of the various molecular weight fractions by size exclusion chromatography. In addition, pre-extracted xylan was subjected to the same dissolution procedure to examine the degradation of low-molecular weight components in more detail.

Erratum to: Dry jet-wet spinning of strong cellulose filaments from ionic liquid solution

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