| 1. |
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| 2. |
- Hedlund, Artur, et al.
(författare)
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Microstructures of cellulose coagulated in water and alcohols from 1-ethyl-3-methylimidazolium acetate : contrasting coagulation mechanisms
- 2019
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Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 26:3, s. 1545-1563
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Tidskriftsartikel (refereegranskat)abstract
- Abstract: Coagulation of cellulose solutions is a process whereby many useful materials with variable microstructures and properties can be produced. This study investigates the complexity of the phase separation that generates the structural heterogeneity of such materials. The ionic liquid, 1-ethyl-3-methylimidazolium acetate ([C2mim][OAc]), and a co-solvent, dimethylsulfoxide (DMSO), are used to dissolve microcrystalline cellulose in concentrations from 5 to 25 wt%. The solutions are coagulated in water or 2-propanol (2PrOH). The coagulated material is then washed and solvent exchanged (water → 2PrOH → butanone → cyclohexane) in order to preserve the generated microstructures upon subsequent drying before analysis. Sweep electron microscopy images of 50 k magnification reveal open-pore fibrillar structures. The crystalline constituents of those fibrils are estimated using wide-angle X-ray spectroscopy and specific surface area data. It is found that the crystalline order or crystallite size is reduced by an increase in cellulose concentration, by the use of the co-solvent DMSO, or by the use of 2PrOH instead of water as the coagulant. Because previous theories cannot explain these trends, an alternative explanation is presented here focused on solid–liquid versus liquid–liquid phase separations. Graphical abstract: [Figure not available: see fulltext.].
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| 3. |
- Karlsson, Mikael, 1978, et al.
(författare)
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Characterisation of silicon, zirconium and aluminium coated titanium dioxide pigments recovered from paint waste
- 2019
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Ingår i: Dyes and Pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 162, s. 145-152
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Tidskriftsartikel (refereegranskat)abstract
- © 2018 Elsevier Ltd Titanium dioxide (TiO2) is the major white pigment used by the paint industry. However, the production of TiO2is associated with a high carbon footprint. An alternative source of pigment could be created by developing a method to recover it from waste paint. In this paper two rutile pigments with different surface treatments were recovered from paint by a thermal recycling process. The pigments were analysed using powder x-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), surface area measurements (BET), laser diffraction for particle size analysis and zeta potential measurements before and after the recycling process. It was concluded that the rutile cores of both pigments were intact and there were no major changes in particle size distribution or surface charge for either pigment induced by the recycling process. However, XPS and zeta potential measurements showed that the surface coating of the pigments can be more or less degraded depending on the chemical nature, which might imply the need for further re-coating after-treatment. Another option would be to find another application for the pigment where the quality and function of the coating is of less importance.
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| 4. |
- Li, Jing, et al.
(författare)
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Towards the mechanism of electrochemical activity and self-healing of 1 wt% PTSA doped polyaniline in alkyd composite polymer coating : Combined AFM-based studies
- 2016
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Ingår i: RSC Advances. - : Royal Society of Chemistry. - 2046-2069. ; 6:23, s. 19111-19127
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Tidskriftsartikel (refereegranskat)abstract
- A composite solvent-borne alkyd coating with 1 wt% p-toluene sulfonic acid (PTSA) doped polyaniline (PANI) was prepared. The mechanisms of electrochemical activity and self-healing properties of the composite coating were investigated by in situ atomic force microscopy (AFM), intermodulation AFM (ImAFM), electrochemical controlled (EC)-AFM combined with cyclic voltammetry (CV), Kelvin force microscopy (KFM), and Fourier transform infrared spectroscopy (FTIR), as well as open-circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) methods. The ImAFM demonstrates the multiphase structure of the composite coating and a high compatibility between the doped PANI and alkyd matrix. The CV and EC-AFM results reveal a high electrochemical activity of the doped PANI in the composite coating as well as reversible redox reactions between the emeraldine salt (ES) and leuco emeraldine base (LB) forms. The Volta potential mapping of KFM demonstrates a strong self-healing ability of the doped PANI in air conditions. The good electrochemical connection between the fine network of PANI in the composite coating and metal surface underneath enable the occurrence of reversible redox reaction between the ES/LB forms of doped PANI and a concomitant release of dopant anions both in air and in 3 wt% NaCl solution as demonstrated by OCP and EIS results. These therefore lead to the strong passivation and self-healing effect of the composite coated on the carbon steel surface.
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| 5. |
- Pradhan, Sulena, et al.
(författare)
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Effect of sonication on particle dispersion, administered dose and metal release of non-functionalized, non-inert metal nanoparticles
- 2016
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Ingår i: Journal of nanoparticle research. - : Springer. - 1388-0764 .- 1572-896X. ; 18:9
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Tidskriftsartikel (refereegranskat)abstract
- In this study, we elucidate the effect of different sonication techniques to efficiently prepare particle dispersions from selected non-functionalized NPs (Cu, Al, Mn, ZnO), and corresponding consequences on the particle dose, surface charge and release of metals. Probe sonication was shown to be the preferred method for dispersing non-inert, non-functionalized metal NPs (Cu, Mn, Al). However, rapid sedimentation during sonication resulted in differences between the real and the administered doses in the order of 30–80 % when sonicating in 1 and 2.56 g/L NP stock solutions. After sonication, extensive agglomeration of the metal NPs resulted in rapid sedimentation of all particles. DLVO calculations supported these findings, showing the strong van der Waals forces of the metal NPs to result in significant NP agglomeration. Metal release from the metal NPs was slightly increased by increased sonication. The addition of a stabilizing agent (bovine serum albumin) had an accelerating effect on the release of metals in sonicated solutions. For Cu and Mn NPs, the extent of particle dissolution increased from <1.6 to ~5 % after sonication for 15 min. A prolonged sonication time (3–15 min) had negligible effects on the zeta potential of the studied NPs. In all, it is shown that it is of utmost importance to carefully investigate how sonication influences the physico-chemical properties of dispersed metal NPs. This should be considered in nanotoxicology investigations of metal NPs. Graphical Abstract: [Figure not available: see fulltext.]
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| 6. |
- Andersson Trojer, Markus, et al.
(författare)
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Elastic strain-hardening and shear-thickening exhibited by thermoreversible physical hydrogels based on poly(alkylene oxide)-grafted hyaluronic acid or carboxymethylcellulose
- 2020
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Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry. - 1463-9076 .- 1463-9084. ; 22:26, s. 14579-14590
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Tidskriftsartikel (refereegranskat)abstract
- The formation of strongly elastic physical gels based on poly(alkylene oxide)-grafted hyaluronan or carboxymethylcellulose, exhibiting both shear-thickening and strain-hardening have been studied using rheometry and explained using a slightly different interpretation of the transient network theory. The graft copolymers were prepared by a quantitative coupling reaction. Their aqueous solutions displayed a thermoreversible continuous transition from Newtonian fluid to viscoelastic solid which could be controlled by the reaction conditions. The evolution of all material properties of the gel could be categorized into two distinct temperature regimes with a fast evolution at low temperatures followed by a slow evolution at high temperatures. The activation energy of the zero shear viscosity and the relaxation time of the graft inside the interconnecting microdomains were almost identical to each other in both temperature regimes. This suggests that the number of microdomains remained approximately constant whereas the aggregation number inside the microdomains increased according to the binodal curve of the thermosensitive graft.
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| 7. |
- Carmona, Pierre, 1995, et al.
(författare)
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Structure formation and coarsening kinetics of phase-separated spin-coated ethylcellulose/hydroxypropylcellulose films
- 2022
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Ingår i: Soft Matter. - : Royal Society of Chemistry. - 1744-683X .- 1744-6848. ; 18:16, s. 3206-3217
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Tidskriftsartikel (refereegranskat)abstract
- Porous phase-separated ethylcellulose/hydroxypropylcellulose (EC/HPC) films are used to control drug transport from pharmaceutical pellets. The drug transport rate is determined by the structure of the porous films that are formed as water-soluble HPC leaches out. However, a detailed understanding of the evolution of the phase-separated structure in the films is lacking. In this work, we have investigated EC/HPC films produced by spin-coating, mimicking the industrial fluidized bed spraying. The aim was to investigate film structure evolution and coarsening kinetics during solvent evaporation. The structure evolution was characterized using confocal laser scanning microscopy and image analysis. The effect of the EC:HPC ratio (15 to 85 wt% HPC) on the structure evolution was determined. Bicontinuous structures were found for 30 to 40 wt% HPC. The growth of the characteristic length scale followed a power law, L(t) ∼ t(n), with n ∼ 1 for bicontinuous structures, and n ∼ 0.45-0.75 for discontinuous structures. The characteristic length scale after kinetic trapping ranged between 3.0 and 6.0 μm for bicontinuous and between 0.6 and 1.6 μm for discontinuous structures. Two main coarsening mechanisms could be identified: interfacial tension-driven hydrodynamic growth for bicontinuous structures and diffusion-driven coalescence for discontinuous structures. The 2D in-plane interface curvature analysis showed that the mean curvature decreased as a function of time for bicontinuous structures, confirming that interfacial tension is driving the growth. The findings of this work provide a good understanding of the mechanisms responsible for morphology development and open for further tailoring of thin EC/HPC film structures for controlled drug release. © 2022 The Royal Society of Chemistry
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| 8. |
- Gao, Jiajia, et al.
(författare)
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Light-induced electrolyte improvement in cobalt tris(bipyridine)-mediated dye-sensitized solar cells
- 2019
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 7:33, s. 19495-19505
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Tidskriftsartikel (refereegranskat)abstract
- Lithium-ion-free tris(2,2′-bipyridine) Co(ii/iii)-mediated electrolytes have previously been proposed for long-term stable dye-sensitized solar cells (DSSCs). Such redox systems also offer an impressive DSSC performance improvement under light soaking exposure, manifested by an increase in photocurrent and fill factor without the expense of decreasing photovoltage. Kinetic studies show that charge transfer and ion diffusion at the electrode/electrolyte interface are improved due to the light exposure. Control experiments reveal that the light effect is unambiguously associated with electrolyte components, [Co(bpy)3]3+ and the Lewis-base additive tert-butylpyridine (TBP). Electrochemical and spectroscopic investigation of the [Co(bpy)3]3+/TBP mixtures points out that the presence of TBP, which retards the electrolyte diffusion, however causes an irreversible redox reaction of [Co(bpy)3]3+ upon light exposure that improves the overall conductivity. This discovery not only provides a new strategy to mitigate the typical Jsc-Voc trade-off in Co(ii/iii)-mediated DSSCs but also highlights the importance of investigating the photochemistry of a photoelectrochemical system.
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| 9. |
- Karlsson, Mikael, 1978, et al.
(författare)
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Surface properties of recycled titanium oxide recovered from paint waste
- 2018
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Ingår i: Progress in organic coatings. - : Elsevier BV. - 0300-9440 .- 1873-331X. ; 125, s. 279-286
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Tidskriftsartikel (refereegranskat)abstract
- Aluminium oxide coated rutile pigment was extracted from a paint matrix by means of a thermal recycling process. The objective was to investigate the effect of the recycling process on the surface properties of the pigment. The pigment was analysed using powder x-ray diffraction (XRD), surface area measurements (BET), laser diffraction for particle size analysis and X-ray photoelectron spectroscopy (XPS) before and after the recycling process. Investigations on the zeta potential and the surface charge were performed as well. It was concluded that the rutile crystalline core and the aluminium oxide coating of the pigment were still intact after the recycling process. The particle size distribution of the recycled pigment was slightly broader compared to the virgin pigment. The measured magnitude in zeta potential of the recycled pigment was lower than for the virgin pigment. This difference is thought to be caused by alteration in the surface hydroxyl concentration. Surface charge titrations showed differences between the virgin and the recycled pigment at alkaline pH and at low salt concentrations.
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| 10. |
- Maffre, Marion, et al.
(författare)
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Investigation of Electrochemical and Chemical Processes Occurring at Positive Potentials in "Water-in-Salt" Electrolytes
- 2021
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Ingår i: Journal of the Electrochemical Society. - : The Electrochemical Society. - 1945-7111 .- 0013-4651. ; 168:5
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Tidskriftsartikel (refereegranskat)abstract
- Lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) based water-in-salt electrolytes (WiSEs) has recently emerged as a new promising class of electrolytes, primarily owing to their wide electrochemical stability windows (similar to 3-4 V), that by far exceed the thermodynamic stability window of water (1.23 V). Upon increasing the salt concentration towards superconcentration the onset of the oxygen evolution reaction (OER) shifts more significantly than the hydrogen evolution reaction (HER) does. The OER shift has been explained by the accumulation of hydrophobic anions blocking water access to the electrode surface, hence by double layer theory. Here we demonstrate that the processes during oxidation are much more complex, involving OER, carbon and salt decomposition by OER intermediates, and salt precipitation upon local oversaturation. The positive shift in the onset potential of oxidation currents was elucidated by combining several advanced analysis techniques: rotating ring-disk electrode voltammetry, online electrochemical mass spectrometry, and X-ray photoelectron spectroscopy, using both dilute and superconcentrated electrolytes. The results demonstrate the importance of reactive OER intermediates and surface films for electrolyte and electrode stability and motivate further studies of the nature of the electrode.
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