| 1. |
- Anugwom, Ikenna, et al.
(författare)
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Switchable ionic liquids as delignification solvents for lignocellulosic materials
- 2014
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Ingår i: ChemSusChem. - : John Wiley & Sons. - 1864-5631 .- 1864-564X. ; 7:4, s. 1170-1176
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Tidskriftsartikel (refereegranskat)abstract
- The transformation of lignocellulosic materials into potentially valuable resources is compromised by their complicated structure. Consequently, new economical and feasible conversion/fractionation techniques that render value-added products are intensely investigated. Herein an unorthodox and feasible fractionation method of birch chips (B. pendula) using a switchable ionic liquid (SIL) derived from an alkanol amine (monoethanol amine, MEA) and an organic super base (1,8-diazabicyclo-[5.4.0]-undec-7-ene, DBU) with two different trigger acid gases (CO2 and SO2 ) is studied. After SIL treatment, the dissolved fractions were selectively separated by a step-wise method using an antisolvent to induce precipitation. The SIL was recycled after concentration and evaporation of anti-solvent. The composition of undissolved wood after MEA-SO2 -SIL treatment resulted in 80 wt % cellulose, 10 wt % hemicelluloses, and 3 wt % lignin, whereas MEA-CO2 -SIL treatment resulted in 66 wt % cellulose, 12 wt % hemicelluloses and 11 wt % lignin. Thus, the MEA-SO2 -SIL proved more efficient than the MEA-CO2 -SIL, and a better solvent for lignin removal. All fractions were analyzed by gas chromatography (GC), Fourier transform infrared spectroscopy (FT-IR), (13) C nuclear magnetic resonance spectroscopy (NMR) and Gel permeation chromatography (GPC).
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| 2. |
- Anugwom, Ikenna, et al.
(författare)
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Towards optimal selective fractionation for Nordic woody biomass using novel amine–organic superbase derived switchable ionic liquids (SILs)
- 2014
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Ingår i: Biomass and Bioenergy. - : Elsevier. - 0961-9534 .- 1873-2909. ; 70, s. 373-381
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Tidskriftsartikel (refereegranskat)abstract
- Abstract Improved fractionation process conditions for wood dissolution with switchable ionic liquids (SILs) were determined. The short time, high temperature (STHT) system was introduced as a selective and efficient way to extract components from lignocellulosic material. A SIL based on monoethanol amine (MEA) and 1,8-diazabicyclo-[5.4.0]-undec-7-ene (DBU) formed via coupling with SO2, was applied as a solvent in a 1:3 weight ratio with water. In essence, selective dissolution of mainly lignin was achieved by means of the aqueous SIL at 160 °C (∼6.1 bar corresponding to the vapor pressure of water) in 2 h and in a pressure vessel, for both hard- and soft-wood. About 95 wt-% of wood lignin was extracted. The dissolved components in the spent SIL were recovered by the addition of an anti-solvent whereupon over 70% of the dissolved components were recovered; the recovered fraction contained 19 wt-% hemicellulose while the rest of the material was in essence lignin. The non-dissolved, fluffy material contained ∼70 wt-% cellulose and ∼20 wt-% hemicellulose – a consistency resembling that of Kraft pulp.
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| 3. |
- Asaadi, Shirin, et al.
(författare)
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Structural analysis of Ioncell-F fibres from birch wood
- 2018
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Ingår i: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617. ; 181, s. 893-901
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Tidskriftsartikel (refereegranskat)abstract
- Quite recently, the Ioncell-F process, a novel and promising Lyocell fibre process, has been developed. The ionic liquid 1,5-diazabicyclo[4.3.0]non-5-enium acetate ([DBNH]OAc) utilized in this process, was identified as an excellent cellulose solvent for dry-jet wet fibre spinning. Fibres spun from cellulose-[DBNH]OAc solution have shown excellent mechanical properties. Herein, various structural features of these ionic liquid-based fibres were analyzed and correlated with their mechanical properties. The highest slope of tenacity increase of these Ioncell-F fibres (from birch wood) observed at low draw ratios (DRs), while a continuous but slower increase occurs to partly very high draws. The improvements in the mechanical properties do not seem to correlate with changes in the crystallite size or the crystalline orientation based on wide-angle X-ray scattering (WAXS) results. More significant differences were seen for the sample crystallinity, the amorphous orientation (measured by birefringence), the orientation of the voids, the specific surface (measured by small-angle X-ray scattering (SAXS)), and the sorption/desorption properties of the fibres.
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| 4. |
- Baird, Zachariah Steven, et al.
(författare)
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Vapor-Liquid Equilibrium of Ionic Liquid 7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-enium Acetate and Its Mixtures with Water
- 2020
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Ingår i: Journal of Chemical and Engineering Data. - : American Chemical Society (ACS). - 0021-9568 .- 1520-5134. ; 65:5, s. 2405-2421
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Tidskriftsartikel (refereegranskat)abstract
- Ionic liquids have the potential to be used forextracting valuable chemicals from raw materials. These processesoften involve water, and after extraction, the water or otherchemicals must be removed from the ionic liquid, so it can bereused. To help in designing such processes, we present data onthe vapor−liquid equilibrium of the system containing protic ionicliquid 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-enium acetate,water, acetic acid, and 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene. Earlier studies have only focused on mixtures of water and anionic liquid with a stoichiometric ratio of the ions. Here, we alsoinvestigated mixtures containing an excess of the acid or basecomponent because in real systems with protic ionic liquids, theamount of acid and base in the mixture can vary. We modeled thedata using both the ePC-SAFT and NRTL models, and we compared the performance of different modeling strategies. We alsoexperimentally determined the vapor composition for a few of the samples, but none of the modeling strategies tested couldaccurately predict the concentration of the acid and base components in the vapor phase.
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| 5. |
- Borrega, Marc, et al.
(författare)
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Birch wood pre-hydrolysis vs pulp post-hydrolysis for the production of xylan-based compounds and cellulose for viscose application
- 2018
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Ingår i: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617 .- 1879-1344. ; 190, s. 212-221
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Tidskriftsartikel (refereegranskat)abstract
- Hydrothermal treatments of birch wood and kraft pulp were compared for their ability to extract the xylan and produce viscose-grade pulp. Water post-hydrolysis of kraft pulp produced a high-purity cellulosic pulp with lower viscosity but higher cellulose yield than traditional pre-hydrolysis kraft pulping of wood. Post-hydrolysis of pulp also increased the crystallite dimensions and degree of crystallinity in cellulose, and promoted a higher extent of fibril aggregation. The lower specific surface area in post-hydrolyzed pulps, derived from their larger fibril aggregates, decreased the accessibility of –OH groups. However, this lower accessibility did not seem to decrease the pulp reactivity to derivatizing chemicals. In the aqueous side-stream, the xylose yield was similar in both pre- and post-hydrolysates, although conducting post-hydrolysis of pulp in a flow-through system enabled the recovery of high purity and molar mass (∌10 kDa) xylan for high-value applications.
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| 6. |
- Brännvall, Elisabet
(författare)
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Aspects on Strenght Delivery and Higher Utilisation of the Strength Potential of Kraft Pulp Fibres
- 2007
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Studies on strength delivery and related fields have so far concentrated on finding the locations in the mill where fibres are damaged and what the damages consist of. However, fibres will invariably encounter mechanical stresses along the fibreline and in this thesis a new concept is introduced; the vulnerability of fibres to mechanical treatment. It is hypothesised that fibres with different properties have different abilities to withstand the mechanical forces they endure as they are discharged from the digester and transported through valves, pumps and various washing and bleaching equipment. In the thesis, results are presented from trials where pulps with significantly different hemicellulose compositions were high-intensity mixed at pH 13, 70°C and 10% pulp consistency and pulp strength evaluated. By varying alkalinity and temperature, pulps with different carbohydrate composition could be obtained. High alkali concentration and low temperature resulted in high glucomannan content and low xylan content, whereas cooking at low alkali concentration and high temperature rendered a pulp with low glucomannan and high xylan content. The high alkalinity pulp was stronger, determined as tear index at given tensile index. The pulp viscosity was also higher for this pulp. However, when the pulps were subjected to high-intensity mixing, the high alkalinity pulp lost in tear strength and the re-wetted zero-span tensile strength was substantially reduced. The pulp cooked at high alkalinity was thus interpreted as being more vulnerable to mechanical treatment than the pulp obtained by cooking at low alkalinity. Another pair of pulps was manufactured at high and low sodium ion concentrations, but otherwise with similar chemical charges. The pulp obtained by cooking at low sodium ion concentration became stronger, evaluated as tear index at a given tensile index and the curl index was substantially lower, 8% compared to 12% for the pulp cooked at a high sodium ion concentration. The viscosity was 170 ml/g higher for the pulp manufactured at low sodium ion concentration. When the pulps were subjected to high-intensity mixing, the tear strength of the pulp manufactured at high sodium ion concentration was reduced. The re-wetted zero-span tensile index decreased also after mixing. The pulp obtained by cooking at higher sodium ion concentration was thus interpreted as being more vulnerable to mechanical treatment than the pulp manufactured at lower sodium ion concentration. In the thesis, two reasons for the low strength delivery of industrially produced pulps compared to laboratory-cooked pulps are put forward. Since the ionic strength of mill cooking liquor systems is much higher than is normally used in laboratory cooking, this can partly explain the difference in strength between mill- and laboratory-cooked pulp. A higher sodium ion concentration was shown in this thesis work to give a pulp of lower strength. Secondly, it is suggested that the difference in retention time of the black liquor in laboratory cooking and continuous mill cooking systems can explain the difference in tensile strength between laboratory-cooked and mill-produced pulp. The black liquor in a continuous digester has a longer retention time in the digester than the chips. This gives a longer time for the dissolved xylan to degrade and, as a consequence, the xylan deposited on the mill pulp fibres will be more degraded than the xylan deposited on the laboratory-cooked pulp fibres. In the thesis, results are also presented from studies using different strength-enhancing chemicals. The fibre surfaces of bleached never-dried and once-dried pulp were modified by the polyelectrolyte multilayer technique using cationic and anionic starch. Although the pulps absorbed the same amount of starch, the never-dried pulp reached a higher tensile index than the once-dried pulp. When the starch-treated never-dried pulp was dried and reslushed it still had higher tensile index than the never-dried untreated pulp. The starch layers were thus able to counteract part of the hornification effect. The never-dried starch treated pulps were subsequently dried, reslushed and beaten. Pulp with starch layers had a better beatability evaluated as the tensile index obtained after given number of PFI revolutions than dried untreated pulp. Hence, there is a potential to increase the tensile index of market pulp by utilising the polyelectrolyte multilayer technique before drying. Addition of CMC to bleached mill pulp and laboratory-cooked pulp increased the tensile strength to the same degree for both pulps. CMC addition had a straightening effect on the fibres, the shape factor increased and this increased the zero-span tensile strength also.
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| 7. |
- Chawachart, Niwat, et al.
(författare)
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Thermal behaviour and tolerance to ionic liquid [emim] OAc in GH10 xylanase from Thermoascus aurantiacus SL16W
- 2014
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Ingår i: Extremophiles. - : Springer Japan. - 1431-0651 .- 1433-4909. ; 18:6, s. 1023-1034
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Tidskriftsartikel (refereegranskat)abstract
- GH10 xylanase from Thermoascus aurantiacus strain SL16W (TasXyn10A) showed high stability and activity up to 70–75 C. The enzyme’s half-lives were 101 h, 65 h, 63 min and 6 min at 60, 70, 75 and 80 C, respectively. The melting point (Tm), as measured by DSC, was 78.5 C, which is in line with a strong activity decrease at 75–80 C. The biomass-dissolving ionic liquid 1-ethyl-3-methylimidazolium acetate ([emim]OAc) in 30 % concentration had a small effect on the stability of TasXyn10A; Tm decreased by only 5 C. It was also observed that [emim]OAc inhibited much less GH10 xylanase (TasXyn10A) than the studied GH11 xylanases. The Km of TasXyn10A increased 3.5-fold in 15 % [emim]OAc with xylan as the substrate, whereas the approximate level of Vmax was not altered. The inhibition of enzyme activity by [emim]OAc was lesser at higher substrate concentrations. Therefore, high solid concentrations in industrial conditions may mitigate the inhibition of enzyme activity by ionic liquids. Molecular docking experiments indicated that the [emim] cation has major binding sites near the catalytic residues but in lower amounts in GH10 than in GH11 xylanases. Therefore, [emim] cation likely competes with the substrate when binding to the active site. The docking results indicated why the effect is lower in GH10.
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| 8. |
- Colson, Jérôme, et al.
(författare)
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Adhesion properties of regenerated lignocellulosic fibres towards poly(lactic acid) microspheres assessed by colloidal probe technique
- 2018
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 1095-7103 .- 0021-9797. ; 532, s. 819-829
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Tidskriftsartikel (refereegranskat)abstract
- In the field of polymer reinforcement, it is important to understand the interactions involved between the polymer matrix and the reinforcing component. This paper is a contribution to the fundamental understanding of the adhesion mechanisms involved in natural fibre reinforced composites. We report on the use of the colloidal probe technique for the assessment of the adhesion behaviour between poly(lactic acid) microspheres and embedded cross-sections of regenerated lignocellulosic fibres. These fibres consisted of tailored mixtures of cellulose, lignin and xylan, the amount of which was determined beforehand. The influence of the chemical composition of the fibres on the adhesion behaviour was studied in ambient air and in dry atmosphere. In ambient air, capillary forces resulted in larger adhesion between the sphere and the fibres. Changing the ambient medium to a dry nitrogen atmosphere allowed reducing the capillary forces, leading to a drop in the adhesion forces. Differences between fibres of distinct chemical compositions could be measured only on freshly cut surfaces. Moreover, the surface energy of the fibres was assessed by inverse gas chromatography. Compared to fibres containing solely cellulose, the presence of lignin and/or hemicellulose led to higher adhesion and lower surface energy, suggesting that these chemicals could serve as natural coupling agents between hydrophobic and hydrophilic components.
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| 9. |
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| 10. |
- Darabi, Sozan, 1994, et al.
(författare)
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Green Conducting Cellulose Yarns for Machine-Sewn Electronic Textiles
- 2020
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 12:50, s. 56403-56412
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Tidskriftsartikel (refereegranskat)abstract
- The emergence of "green"electronics is a response to the pressing global situation where conventional electronics contribute to resource depletion and a global build-up of waste. For wearable applications, green electronic textile (e-textile) materials present an opportunity to unobtrusively incorporate sensing, energy harvesting, and other functionality into the clothes we wear. Here, we demonstrate electrically conducting wood-based yarns produced by a roll-to-roll coating process with an ink based on the biocompatible polymer:polyelectrolyte complex poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS). The developed e-textile yarns display a, for cellulose yarns, record-high bulk conductivity of 36 Scm-1, which could be further increased to 181 Scm-1 by adding silver nanowires. The PEDOT:PSS-coated yarn could be machine washed at least five times without loss in conductivity. We demonstrate the electrochemical functionality of the yarn through incorporation into organic electrochemical transistors (OECTs). Moreover, by using a household sewing machine, we have manufactured an out-of-plane thermoelectric textile device, which can produce 0.2 μW at a temperature gradient of 37 K.
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