Superbase-based protic ionic liquids for cellulose filament spinning

Cellulosic fibers long dominated the man-made fiber market until the synthetic fiber production surpassed cellulosics in the late 1960s (The Fiber Year 2013). Ever since, the man-made cellulose fibers have been in the shadow of polyesters, polyamides and acrylics. However, more and more problems are emerging in connection with the ubiquitous use of plastics. For instance, an increasing share of the plastic debris is discharged during laundering and enters the marine environment, where weathering causes fragmentation into so-called secondary microplastics that even small marine invertebrates may ingest (Goldstein and Goodwin 2013). By 2100, a 50-fold increase of buoyant microplastic particles (ca. 50 particles m⁻³) and ca. 8000 particles kg⁻¹ of sedimented microplastic particles are predicted (Everaert et al. 2018). This and other environment and health-threatening issues have led to a renaissance of cellulosic fibers. In 2018, the total man-made cellulosics production was 6.8 million tonnes, with viscose accounting for 5.6 million tonnes (The Fiber Year 2019). The viscose technology, however, is associated with a number of drawbacks and limitations. It consists of a long processing cascade and requires large amounts of CS₂ and caustic, which results in hazardous byproducts such as H₂S gases and other volatile thio-compounds posing severe threats on the environment and work forces. Alternative solutions to satisfy the increasing demand for cellulosic fibers are thus needed. At present, only one lyocell-type fiber has a noteworthy share on the fiber market. Lyocell is a generic name which is derived from the Greek word lyein (meaning dissolve) and cell from cellulose, and describes a process in which cellulose is dissolved without chemical modification in a direct solvent and spun in a dry-jet wet spinning process via an air gap into an aqueous coagulation bath. Currently, the only commercial lyocell solution is based on the solvent N-methylmorpholine N-oxide (NMMO) monohydrate. With the development starting as early as in the late 1960s, the first commercial production plant started operation in the early 1990s. In 2018, this fiber type, sold under the trademark Tencel, had a market volume of ca. 220,000 annual tones with another 100,000 tonnes plant being built. The continuous expansion of the global lyocell capacity reflects the increasing demand for sustainably produced bio-based fibers. This and certain stability issues associated with NMMO (Buijtenhuijs et al. 1986; Rosenau et al. 2001; Jusner et al. 2020), have motivated research on other cellulose solvents that allow for direct dissolution and subsequent fiber spinning. Meanwhile, a wide spectrum of cellulose solvent systems is known, including electrolyte solutions [DMAc/LiCl (Hansen and Björkman 1998), DMSO/TBAF (Heinze et al. 2000; Köhler and Heinze 2007), ammonia or amine/thiocyanate (Hattori et al. 2002, 2004), [BMIM]Cl/DMI (Rinaldi 2011)], phosphoric acids (Bredereck and Hermanutz 2005; Liebert 2010), metal complex-based solvents (Horvath 2006; Liebert 2010), and aqueous sodium hydroxide (with and without additives) (Budtova and Navard 2016; Kamida et al. 1984; Kamide et al. 1992; Yamashiki et al. 1992). However, all of them suffer from certain problems and shortcomings which have yet prevented them from scaling-up to commercially relevant levels.

Strictly speaking, this also applies to ionic liquids (ILs) which are the subject of the article at hand. Although ILs have been described already at the beginning of the 20th century (Walden 1914), notable research activities in this field emerged only in the 1990s. The definition of ILs and a comprehensive overview can be found in the seminal review by Welton (1999). At the beginning of the 21st century, ILs were found to dissolve biopolymers such as cellulose, but also secondary wood polymers (hemicellulose, lignin) and wood in its entirety. For details, the reader is referred to a set of earlier published reviews (Brandt et al. 2013; Lê et al. 2019; Maeki-Arvela et al. 2010; Pinkert et al. 2009; Singh and Simmons 2013; Wang et al. 2012). Notably, most of the described biomass-dissolving ILs were imidazolium-based and only very few comprised other heterocycles such as 1-alkylpyridinium, 1-alkyl-1-methylpyrrolidinium, and guanidinium or non-cyclic quaternary cations like tetraalkylammonium and phosphonium ions (El Seoud et al. 2007; Laus et al. 2005; Maeki-Arvela et al. 2010). Further, they all included an anion with a high hydrogen-bond (net) basicity (Crowhurst et al. 2003; Doherty et al. 2010; Hauru et al. 2012). The most prominent ones regarding cellulose-dissolving ILs are halides (Swatloski et al. 2002), carboxylates (Fukaya et al. 2006), and phosphates (Brandt et al. 2010; Fukaya et al. 2008). Various ILs representing combinations of above mentioned cations and anions have been proposed for spinning of (ligno-)cellulosic filaments. A comprehensive summary of IL-based fiber spinning was given earlier (Hummel et al. 2016). The majority of those studies focus on imidazolium chlorides and acetates. They can dissolve cellulose and other biopolymers in high concentrations, and in particular imidazolium acetate ILs are characterized by low viscosity, facilitating handling and dissolution. Yet, imidazolium-ILs suffer from a number of drawbacks limiting their potential for large-scale fiber spinning. Usually, the halide-containing IL require a comparatively high dissolution and processing temperatures at which the IL can decompose (Kosmulski et al. 2004; Meine et al. 2010), and cellulose polymers are degraded substantially even if stabilizers are added (Bentivoglio et al. 2006; Gazit and Katz 2012; Laus et al. 2005). These problems can be alleviated to some extent when replacing the halide anion with acetate (Michud et al. 2015a). Nonetheless, side reactions induced by the imidazolium moiety such as cellulose modification (Clough et al. 2015; Ebner et al. 2008) and acetylation through trans-acylation may occur (Zweckmair et al. 2015).

Apart from thermal and chemical integrity, the spinning of filaments requires distinct visco-elastic properties of the cellulose-IL solutions. These requirements are less strict for wet spinning where the coagulation of the filaments happens instantly after the solutions exit the spinneret. Hence, no or very limited draw is applied to the filament. Consequently, the total orientation and crystallinity of the resulting fibers are low, resulting in moderate mechanical properties. In contrast, dry-jet wet spinning results in filaments and fibers with a pronounced macromolecular orientation and high mechanical properties. The decisive difference between wet and dry-jet wet spinning is that in the case of the latter the spinneret is outside the spin bath and the visco-elastic filaments pass through an air gap (typically only a few centimeters long) before they immerge into a coagulating medium. By adjusting the filament take-up velocity to a multiple of the linear extrusion velocity, the filaments are stretched predominately in the air gap. Once the filaments get into contact with the spin bath rapid solvent exchange causes instant coagulation which is believed to follow spinodal decomposition (Nishiyama et al. 2019). The stretch of the filament is called draw and creates a uniaxial stress tensor acting on the polymer chains in solution. The polymers adopt an oriented structure with a predominant direction parallel to the filament axis, which is preserved in the final solid fiber due to the rapid solidification in the spin bath. This axial orientation results in high tensile strength and modulus known for lyocell-type fibers and is usually not accessible through classical wet-spinning processes.

Evidently, the filament draw also reduces the diameter of the final cellulosic fiber. A final fiber diameter of ca. 10–13 µm (correspond to 1–2 dtex) is mandatory for technical applications such as composite reinforcement and in particular to produce yarns for textiles and clothing. Although the reduction of the diameter may seem trivial, it is one of the key issues that disqualifies most cellulose-IL solutions, which lack the necessary viscoelasticity for filament draw. Various breaching mechanisms in the air gap depend on the initial filament diameter, which limits the minimum diameter of the spinneret orifices (Ziabicki and Takserman-Krozer 1964a, b). If the filament is too thin when exiting the spinneret it will breach in the air gap. Thus, the draw-ability of an initially thick filament is a central requirement for dry-jet wet spinning to yield thin and strong fibers. The archetypical IL [emim]OAc does not provide the addressed viscoelasticity and its suitability as solvent for dry-jet wet spinning is thus limited (Hauru et al. 2016).

We found earlier that the amidine-based ionic liquid 1,5-diazabicyclo[4.3.0]non-5-ene-1-ium acetate ([DBNH]OAc) is an excellent solvent to process cellulose in a lyocell-type spin process (Hummel et al. 2016; Michud et al. 2016b; Sixta et al. 2015). It contains acetate as an established anion that provides the necessary hydrogen bond basicity to dissolve cellulose. Obtained through simple mixture of the superbase with equimolar acetic acid, the resulting IL dissolves lignocellulose rapidly at mild processing temperatures (≤ 80 °C). More importantly, the resulting solutions depict visco-elastic properties suitable for dry-jet wet spinning at high draw ratios (up to 20) (Ma et al. 2016a). After studying systematically the influence of the composition (Ma et al. 2016a, b) and molecular weight distribution (Michud et al. 2015b) of the lignocellulosic solute on the spinnability, we now looked at alternative superbase-based ILs: 1,8-Diazabicyclo[5.4.0]undec-7-enium acetate ([DBUH]OAc), an amidine-based IL, and 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-enium acetate ([mTBDH]OAc), a guanidine-based IL. Similar to DBN, both DBU and mTBD ILs are capable of dissolving high cellulose contents (Parviainen et al. 2013; Kuzmina et al. 2017; Elsayed et al. 2020). Herein, we report on the suitability of these ILs as spinning solvents and compare their performance with NMMO monohydrate as a benchmark.

The superbases were received as follows; DBN (Fluorochem, United Kingdom), DBU (Merck, Germany), and mTBD (BOC Sciences, USA). Respective ILs were prepared by the addition of equimolar glacial acetic acid (Merck, Germany) to the superbases (DBN, DBU and mTBD). [emim]OAc was available from Merck, Germany. The IL preparation was carried out in a controlled temperature glass reactor under continuous stirring for 1 h. The reaction temperature was set to 70 °C for the synthesis of [DBNH]OAc and [DBUH]OAc, and 80 °C for the synthesis of [mTBDH]OAc. NMMO monohydrate (Alfa Aesar, Germany) was used as received. Propyl gallate powder (Merck, Germany) and NaOH pellets (VWR, Finland) were used as stabilizers during the NMMO dope preparation. Cellulose pulp sheets, birch prehydrolysis kraft (PHK) (intrinsic viscosity = 494 ml/g, Mw = 160.5 kD_a, polydispersity index 3.6, Pure by Stora Enso, Enocell mill, Finland), was received and ground in a Wiley mill.

Cellulose dissolution took place in a vertical kneader by adding 13 wt% of cellulose (of the total mass) to the ILs and NMMO, respectively. An additional 0.3 wt% (oven-dry mass of pulp) propyl gallate and 0.13 wt% (oven-dry mass of pulp) NaOH were added to the NMMO/pulp mixture prior to mixing. Thereafter, the kneader was closed and let to stir for 90 min with 30 RPM under a vacuum pressure of 20 mbar. The applied temperature was 80 °C for the [DBNH]OAc-cellulose and [emim]OAc-cellulose solutions, 85 °C for [mTBDH]OAc-cellulose solution and 95 °C for [DBUH]OAc and NMMO-cellulose solutions. Following dissolution, the cellulose-IL solutions also referred to as dopes, were filtrated in a hydraulic press system (170 bar, metal filter fleece, 5–6 μm absolute fineness) to remove any undissolved cellulose particles. Finally, the clear solutions were wrapped and sealed against moisture and preserved in cold room storage.

Fiber spinning was performed by the means of a dry-jet wet piston unit (Fourné Polymertechnik, Germany). The dope was fed to the spinning cylinder and extruded through the spinneret capillaries. The filaments were aligned and stretched in an air gap before regenerating in a ca. 110 L water spin bath and finally collected around a spinning godet. The extrusion velocity was 3.5 m/min, whilst the take-up velocity gradually increased from 7 to 42 m/min, i.e., the draw ratio (DR) range of 2–12. The spinneret was of 200 holes, 100 μm capillary diameter and a length-to-diameter ratio of 0.2. The air gap distance was 1 cm and the temperature of the bath was fixed to 12 °C throughout the process. Over the course of the spinning process, different temperatures were employed for the various dopes. The temperatures were ca. 80 °C for the [DBNH]OAc, 85 °C for the [mTBDH]OAc, and 95 °C [DBUH]OAc and NMMO dopes. Directly after spinning, the regenerated filaments were cut into 10 cm fibers and washed at 80 °C for 2 h to rinse off the residual IL. The washing water was changed to fresh water after the first hour interval.

All superbase-based ILs studied herein dissolved pulp cellulose readily, resulting in solutions with similar rheological properties. The importance of the rheological behavior for the spinnability in the dry-jet wet spinning process has been discussed in detail earlier (Hummel et al. 2016; Michud et al. 2015b). A defined balance between viscous fluidity and elastic behavior is a key parameter. High-throughput extrusion of the dope requires shear thinning upon shear stress in the spin capillary to avoid overly high pressures. The resulting filaments must then depict a certain elasticity to withstand the uniaxial stress exerted through the draw in the air gap before they immerge into the coagulation bath where they solidify (Nishiyama et al. 2019). Oscillatory shear measurements at various temperatures provided the complex viscosity and dynamic moduli for each cellulose-IL solution. As expected, they were all non-Newtonian fluids with strong shear thinning. At low angular frequency, the complex viscosity curves approached the Newtonian plateau. Through WLF time–temperature superposition, the data points could be shifted to even lower angular frequency than accessed during the measurement, making the Newtonian plateau even more visible (Fig. 1, left).

The Cross model was used to fit the complex viscosity and calculate the limiting value further referred to as the “zero shear” viscosity (η₀). However, this value would only correspond to the real (= dynamic) η₀ if the Cox–Merz rule is valid (i.e., complex and dynamic viscosity as function of shear rate and angular frequency, respectively, superimpose perfectly). This has been confirmed by some authors (Haward et al. 2012), whereas others found pronounced differences in complex and dynamic viscosities (Chen et al. 2011; Lu et al. 2012). Using the master curve to calculate the η₀ value should be more accurate since the data set reaches further into the Newtonian plateau. However, we found that the difference between the limiting values calculated from the original data at the respective measurement temperature and those calculated through extrapolation of the master curve were statistically insignificant. Thus, η₀ values can also be calculated straight from the measurement data. Additional information of the η₀ values are available in the ESI Fig. S2.

NMMO and [DBNH]OAc are already known solvents in the lyocell technology. The respective cellulose solutions depict visco-elastic properties adequate for the dry-jet wet spinning (Fink et al. 2001; Hummel et al. 2016; Sixta et al. 2015). The rheological measurements of the dopes prepared with [mTBDH]OAc and [DBUH]OAc revealed similar properties. Figure 1 (left) shows the complex viscosity curves of the pulp solutions from the superbase ILs and NMMO at 90 °C. Both NMMO and [DBUH]OAc dopes express the highest η₀, while [mTBDH]OAc and [DBNH]OAc dopes are slightly lower. At higher angular frequency, all solutions reveal strong shear thinning until the curves virtually superimpose. Storage and loss moduli of the same solutions and temperature are shown in Fig. 1 (right). The differences between the solutions are even less pronounced than for the complex viscosity. As reported already earlier, the regions in which the storage modulus G’ scales with ω² and G’’ scales with ω were outside the measurement range, typical for highly concentrated cellulose solutions (Hummel et al. 2016).

The dynamic moduli also allowed for the calculation of the relaxation time spectrum of the pulp cellulose in the respective IL. Since pulp cellulose is not a monodisperse uniform polymer, each carbohydrate chain is characterized by an individual relaxation time. The resulting relaxation time spectrum can be directly correlated to the molecular weight distribution. Figure 2 (right) shows the relaxation time spectrum of the pulp in each ionic liquid.

H(lambda) is related to the number of molecules or components with a certain relaxation time (Ayad et al. 2001; Fulchiron et al. 1995; Meister and Kosan 2015). Besides differences in intensity of H(lambda)*lambda, the relaxation time spectra of all spinnable solutions have a similar distribution. For comparison, the spectrum of the same pulp cellulose dissolved at 13 wt% in [emim]OAc was added. This particular solution was found non-spinnable under the dry-jet wet conditions applied to all other spin dopes (Hauru et al. 2016). The intensity is significantly reduced, and the maximum shifted to lower relaxation time values. This is in line with the observed reduced elastic and more viscose behavior of the [emim]OAc dope, leading to capillary breach in the air gap and impeding stable spinning (Ziabicki and Takserman-Krozer 1964a, b). A summary of the rheology data can be found in the ESI Table S2.

The temperature dependence of the η₀ is shown in the Arrhenius plot in Fig. 2 (left). The activation energy of flow (E_A) was calculated using the Arrhenius equation η₀ = A*exp(E_A/RT), with R as the universal gas constant and the temperature (T) in K. It was noted earlier that ILs and their polymer solutions might not show a fully linear trend in the Arrhenius plot but rather depict a slightly convex evolution, which is more accurately represented by the Vogel-Fulcher-Tamman equation typically used for glass-forming liquids (Fröba et al. 2008). However, we and others found earlier that a simple Arrhenius fit is sufficiently accurate for a qualitative comparison of the different solutions (Gericke et al. 2009; Hummel et al. 2019). The activation energy of flow was in the range of 57–67 kJ/mol for all pulp solutions studied herein. This values are in line with previously reported activation energies for pulps with a similar DP in ionic liquid (40–70 kJ/mol) (Gericke et al. 2009) or NMMO solutions (40–90 kJ/mol) (Blachot et al. 1998; Gavillon and Budtova 2007).

In numerous earlier studies we have found that the dopes are spinnable at temperatures where the η₀ is in the range of 30 kPa.s and the cross-over point (COP) of the dynamic moduli occurs at 0.8–1.2 s⁻¹ and around 4000 Pa (Hummel et al. 2016; Michud et al. 2015b; Sixta et al. 2015). The spinning temperature was then chosen accordingly so that above criteria were met. The angular frequency of the COP was 0.8 s⁻¹ for [DBNH]OAc at 80 °C, 0.83 s⁻¹ for [mTBD]OAc at 85 °C, 1.17 and 1.02 s⁻¹ for NMMO and [DBUH]OAc at 95 °C, respectively. Although these temperature differences are small, they might have a notable impact on the overall process economics when scaled to commercial scale.

While NMMO and [DBNH]OAc have been established as excellent solvents for cellulose dry-jet wet spinning in numerous studies, good spinnability was also observed for pulp solutions in [mTBDH]OAc and [DBUH]OAc. Homogenous filaments were extruded, drawn in the air gap and regenerated in the coagulation bath. The DR of the filaments could be increased gradually to reach a maximum DR of 12, a value that yields fibers with a linear density of 1.2–1.35 dtex (using spinnerets with a capillary diameter of 100 µm). Throughout the spinning process, no systematic filament breach in the air gap or in the spin bath was noticed apart from a few filament breaks that are inevitable in a batch-type process. Fibers at various DRs were collected for subsequent analyses.

The structural properties of the regenerated fibers are characterized and quantified through various parameters. The total polymer orientation is accessible via birefringence measurements. The crystalline orientation is obtained through diffraction measurements while the amorphous orientation is derived from the crystalline and total orientation as discussed in the materials and methods section. In general, fibers with high crystallinity and crystalline orientation have pronounced strength values. Table 1 summarizes the development of the birefringence and chain orientation parameters as a function of DR for the different solvents.

Interestingly, all fibers show a high total orientation (0.61–0.68) and crystallinity (0.32–0.35) even at a low DR of 2. Moreover, at the same DR, the birefringence value of the fibers is ca. 0.04, which is significantly higher than that of a regular viscose fiber (0.025) (Jiang et al. 2012). The increased axial orientation of the cellulose polymers is attributed to the high shear stress acting on the polymer chains during the draw in the air gap while cellulose is still in the dissolved state. A gradual increase in DR increased the total orientation of [mTBDH]OAc and [DBNH]OAc fibers. However, the effect was far less pronounced in the case of NMMO and [DBUH]OAc fibers. The crystalline orientation developed with higher draws for all solvents. It is noteworthy, that fibers spun from superbase-based ILs exhibited a higher total and crystalline orientation than that of NMMO at DR 12. On the other hand, the increase in DR had little influence on the crystallinity, which was on a high level already at low DR. This is in alignment with our previous findings for [DBNH]OAc fibers (Hummel et al. 2016). In a similar manner, the amorphous orientation was not affected by the higher DRs except for [mTBDH]OAc fibers, which showed an increase from 0.6 to 0.77.

The morphology of the regenerated fibers at DR 2 and 12 was compared via scanning electron microscope (SEM) imaging, presented in Fig. 3.

At a lower DR, the cross-sectional images reveal more irregularities and non-homogeneities present in all the fibers. Polymer orientation is mostly induced by shear forces that occur during the extrusion of the dope through the spin capillaries. The shear strain, however, is only moderate due to the very low aspect ratio of the spin capillaries. At DR 12, the fibers possess a uniform circular cross section with a clearly fibrillar fiber body illustrating the improved orientation. As mentioned earlier, this is due to the predominant elongational polymer orientation in the air gap.

Figure 4 a displays the evolution of tenacity, elongation and linear density of the spun fibers as a function of the DR.

At a low DR of 3, all fibers exhibited linear density of 4.1–5.6 dtex and pronounced tenacities of 33.4–45.6 cN/tex. Compared to viscose fibers of DR 12, the ILs-based fibers possess higher tenacities even at such low draw (Hummel et al. 2016). Further increase in the take-up velocity only strengthened the filaments with minor decrease in the elongation. At the highest applied draw (12), the fibers titer was 1.2–1.3 dtex, ESI Fig. S3. As presented in Fig. 4 b, NMMO fibers showed the best elongation at break (12.4%) with a tensile strength of 46.5 cN/tex. On the other hand, [DBUH]OAc fibers expressed the highest strength (56.3 cN/tex) and a 9.8% elongation. [DBNH]OAc and [mTBDH]OAc fibers had somehow comparable tenacities of 49.5 and 49.9 cN/tex, respectively. However, higher elongation was depicted by the [DBNH]OAc fibers (12.2%) than [mTBDH]OAc fibers (9.8%), indicating that the latter fibers are slightly stiff. This is also shown in the modulus of elasticity of the [mTBDH]OAc and [DBUH]OAc fibers, where due to their lower elongation, they display the most pronounced modulus at DR 12 with 17.4 and 16.2 GPa, respectively. Contrarily, a lower modulus for NMMO (14.4 GPa) and [DBNH]OAc (13.9 GPa) fibers reflects higher elasticity. The elongation figures of the lyocell fibers discussed here are undoubtedly inferior when compared to the regular viscous ones. As explained earlier, this is due to the difference in the mechanism of regeneration of the wet spinning method, which enforces instant regeneration of the filaments once extruded. Hence, forming highly amorphous randomly distributed cellulose chains of low strength. Meanwhile, the fibers elongation can exceed 20% (Hummel et al. 2016).

It is well known that under wet conditions only cotton fibers preserve their strength and can even demonstrate wet-to-dry tenacities > 1. Viscose fibers, contrarily, exhibit considerably lower values of close to or even lower than 0.5 (Hummel et al. 2016).This is associated with the high amorphous orientation of the viscose fibers, which allows the accessibility of water to the inner core, thereby swelling it and cleaving the hydrogen bonds responsible for its strength (Hummel et al. 2016). However, the lyocell fibers, observed in Fig. 4 c, express improved wet-to-dry tenacities with the lowest of 0.85 and highest of 1. The intrinsically high crystallinity and crystalline orientation of the fibers seem to preserve their strength under the wet state.

Whilst all ionic liquids resulted in fibers of high quality, their potential for commercialization also depends on several other factors. [DBNH]OAc solutions could be spun at considerably lower temperatures than the only commercialized solvent NMMO monohydrate. This could offer energy and cost savings. However, the lyocell process requires almost complete solvent recycling to be commercially feasible. The recycling scheme for NMMO has been optimized over several decades and reached a recovery rate of > 99% (Rosenau et al. 2001). This is yet to be developed for ILs. The recovery rate depends on several crucial key points. One is the removal of the residual IL during the fiber washing step, since ILs can exhibit different affinities towards water and cellulose, which may vary the amount of required washing water and subsequently rise the costs because of extended washing lines. Another important feature is the hydrothermal stability of the solvent. Degradations has to be prevented to avoid detrimental solvent losses over the course of multiple cycles in a continuous process operation. For instance, DBN and its salts can undergo hydrolysis and subsequent irreversible amide formation that needs to be prevented or efficiently reversed (Parviainen et al. 2015). Recently, we successfully demonstrated that [mTBDH]OAc could be thermally recovered in the lyocell process without losing its dissolution power (Elsayed et al. 2020). This is due to the higher electron density of the sp²-hybridized carbon of the guanidine that relatively protects the base against water nucleophilic reactions, whereas a fast relief in the ring strain of the amidines is dominant, producing the primary amines (Hyde et al. 2019). When [DBNH]OAc was subjected to the same recycling scheme, significant deviation in the solvent composition was detected that hindered cellulose dissolution in the following cycles (Elsayed et al. 2020).

The presented results show a high potential of IL solvents in the field of regenerated cellulose fibers. All solvents exhibited excellent cellulose dissolution power whilst producing a homogeneous solution adequate for the dry-jet wet spinning process. The rheological properties showed similar visco-elastic behavior for all dopes suitable for dry-jet wet spinning. NMMO and [DBUH]OAc dopes possessed higher complex viscosity and dynamic moduli than the other solvents. Consequently, their spinning process demands a higher temperature than [mTBDH]OAc and [DBNH]OAc dopes. All fibers revealed both high crystallinity and crystalline orientation even at low DRs. Moreover, the tenacities of the superbase-based fibers were moderately above than those of NMMO fibers at DR 12. On the other hand, NMMO fibers had the best elongation that is similar to the [DBNH]OAc fibers. All fibers retained a high wet-to-dry tenacity, which is a unique property of the lyocell technology. In comparison to viscose fibers, the lyocell fibers exhibit higher crystallinity and orientation (higher strength) but lower elongation at break.

While the demonstrated fibers possess high quality, the selection and success of a new solvent for the lyocell process certainly depend on its recyclability. The proof-of-concept of successful and feasible recovery of the ILs is of significant importance for their commercialization. The long-term hydrothermal stability in a closed-loop operation process and the final recovery rate can only be evaluated once the size of the processing equipment exceeds a critical volume. Hence, pilot plant operations are needed to define the equilibrium of the possible degradations and side products from both the solvent and the solute.