| 1. |
- Costa, Carolina, et al.
(författare)
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Lignin enhances cellulose dissolution in cold alkali
- 2021
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Ingår i: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617 .- 1879-1344. ; 274
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Tidskriftsartikel (refereegranskat)abstract
- Aqueous sodium hydroxide solutions are extensively used as solvents for lignin in kraft pulping. These are also appealing systems for cellulose dissolution due to their inexpensiveness, ease to recycle and low toxicity. Cellulose dissolution occurs in a narrow concentration region and at low temperatures. Dissolution is often incomplete but additives, such as zinc oxide or urea, have been found to significantly improve cellulose dissolution. In this work, lignin was explored as a possible beneficial additive for cellulose dissolution. Lignin was found to improve cellulose dissolution in cold alkali, extending the NaOH concentration range to lower values. The regenerated cellulose material from the NaOH-lignin solvents was found to have a lower crystallinity and crystallite size than the samples prepared in the neat NaOH and NaOH-urea solvents. Beneficial lignin-cellulose interactions in solution state appear to be preserved under coagulation and regeneration, reducing the tendency of crystallization of cellulose.
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| 2. |
- Costa, Carolina, et al.
(författare)
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On the formation and stability of cellulose-based emulsions in alkaline systems : Effect of the solvent quality
- 2022
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Ingår i: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617 .- 1879-1344. ; 286
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Tidskriftsartikel (refereegranskat)abstract
- With amphiphilic properties, cellulose molecules are expected to adsorb at the O/W interface and be capable of stabilizing emulsions. The effect of solvent quality on the formation and stability of cellulose-based O/W emulsions was evaluated in different alkaline systems: NaOH, NaOH-urea and tetrabutylammonium hydroxide (TBAH). The optimal solvency conditions for cellulose adsorption at the O/W interface were found for the alkaline solvent with an intermediate polarity (NaOH-urea), which is in line with the favorable conditions for adsorption of an amphiphilic polymer. A very good solvency (in TBAH) and the interfacial activity of the cation lead to lack of stability because of low cellulose adsorption. However, to achieve long-term stability and prevent oil separation in NaOH-urea systems, further reduction in cellulose's solvency was needed, which was achieved by a change in the pH of the emulsions, inducing the regeneration of cellulose at the surface of the oil droplets (in-situ regeneration).
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| 3. |
- Eivazi, Alireza, et al.
(författare)
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On the development of all-cellulose capsules by vesicle-templated layer-by-layer assembly
- 2021
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Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 13:4
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Tidskriftsartikel (refereegranskat)abstract
- Polymeric multilayer capsules formed by the layer-by-layer (LbL) technique are interesting candidates for the purposes of storage, encapsulation, and release of drugs and biomolecules for pharmaceutical and biomedical applications. In the current study, cellulose-based core-shell particles were developed via the LbL technique alternating two cellulose derivatives, anionic carboxymethyl-cellulose (CMC), and cationic quaternized hydroxyethylcellulose ethoxylate (QHECE), onto a cationic vesicular template made of didodecyldimethylammonium bromide (DDAB). The obtained capsules were characterized by dynamic light scattering (DLS), ζ potential measurements, and high-resolution scanning electron microscopy (HR-SEM). DLS measurements reveal that the size of the particles can be tuned from a hundred nanometers with a low polydispersity index (deposition of 2 layers) up to micrometer scale (deposition of 6 layers). Upon the deposition of each cellulose derivative, the particle charge is reversed, and pH is observed to considerably affect the process thus demonstrating the electrostatic driving force for LbL deposition. The HR-SEM characterization suggests that the shape of the core-shell particles formed is reminiscent of the spherical vesicle template. The development of biobased nano-and micro-containers by the alternating deposition of oppositely charged cellulose derivatives onto a vesicle template offers several advantages, such as simplicity, reproducibility, biocompatibility, low-cost, mild reaction conditions, and high controllability over particle size and composition of the shell.
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| 4. |
- Engqvist, Cecilia, et al.
(författare)
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Interactions between single latex particles and silica surfaces studied with AFM
- 2007
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Ingår i: Colloids and Surfaces A. - : Elsevier BV. - 0927-7757 .- 1873-4359. ; 302:03-jan, s. 197-203
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Tidskriftsartikel (refereegranskat)abstract
- The spreading of single styrene-acrylic latex particles on silicon oxide C surfaces was studied using atomic force microscopy (AFM). Three latexes with different glass transition temperature (Tg) were used and the effects of temperature, time and preparation method were investigated. Particle sizes and shape were measured with AFM and the contact angles were calculated. The observed rate for the spreading of latex particles was low and it took several days before the particles reached steady state, even at temperatures well above their T-g. The experimental particle spreading results deviated with two orders of magnitude from predictions Using the WLF equation for polymer diffusion. The deviation could be attributed to polymer-surface interactions that slowed down the particle spreading. The work of adhesion was calculated using two models. The results from using the regular Young-Dupre equation and a modified version of this equation that also included the mechanical properties (E-modulus and Poisson's ratio) of the latexes, were compared. For soft latex particles the results from the two models agreed well and were of the order of 75 J/m(2), but for glassy latexes the Young-Dupre equation underestimated the work of adhesion.
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| 5. |
- Lidenmark, Cecilia, et al.
(författare)
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Changes with aging in the surface hydrophobicity of coated paper
- 2010
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Ingår i: Tappi Journal. - 0734-1415. ; 9:5, s. 40-46
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Tidskriftsartikel (refereegranskat)abstract
- Time-dependent changes in the surface properties of coated papers were studied as the evolution of surface hydrophobicity of laboratory and commercially coated papers. We measured the apparent contact angles on the papers during several weeks post-production. Hydrophobicity upon aging increased for all samples made from traditional coating colors on mechanical base stock and on base stock made from cotton linters. Accelerated aging by heat treatment intensified the increase of the apparent contact angles and accelerated the time-dependent behavior. A key mechanism in these changes may be the spreading of latex particles in a coating.
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| 6. |
- Lidenmark, Cecilia, 1976-, et al.
(författare)
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The adhesive behavior of extracted latex polymers towards silicon oxide and cellulose
- 2013
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Ingår i: International Journal of Adhesion and Adhesives. - : Elsevier. - 0143-7496 .- 1879-0127. ; 44, s. 250-258
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Tidskriftsartikel (refereegranskat)abstract
- The objective with this work is to compare the adhesive behavior for latex polymers of different glass transition temperatures (T-g) at different length scales and with different contact times. This is accomplished by two techniques: AFM colloidal probe force measurements and JKR-measurements. The aim is to compare the results from these two techniques and relate them to the interaction of the latex polymers towards oxidized silicon wafers and silica/cellulose probes. Theory suggests that altering the short timeframes used in the colloidal probe technique does not affect the ranking of the adhesion for the different polymers, but for the macroscopic JKR-technique it influences the measured work of adhesion. It is therefore important to let the system reach a steady state before assuming complete spreading and adhesion. AFM and JKR measurements showed the same trends where the polymer with lowest content of styrene has the lowest T-g and the highest adhesion, due to the larger polymer chain mobility.
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| 7. |
- Lindman, Björn, et al.
(författare)
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Hydrophobic interactions control the self-assembly of DNA and cellulose
- 2021
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Ingår i: Quarterly reviews of biophysics (Print). - 0033-5835 .- 1469-8994. ; 54
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Tidskriftsartikel (refereegranskat)abstract
- Desoxyribosenucleic acid, DNA, and cellulose molecules self-assemble in aqueous systems. This aggregation is the basis of the important functions of these biological macromolecules. Both DNA and cellulose have significant polar and nonpolar parts and there is a delicate balance between hydrophilic and hydrophobic interactions. The hydrophilic interactions related to net charges have been thoroughly studied and are well understood. On the other hand, the detailed roles of hydrogen bonding and hydrophobic interactions have remained controversial. It is found that the contributions of hydrophobic interactions in driving important processes, like the double-helix formation of DNA and the aqueous dissolution of cellulose, are dominating whereas the net contribution from hydrogen bonding is small. In reviewing the roles of different interactions for DNA and cellulose it is useful to compare with the self-assembly features of surfactants, the simplest case of amphiphilic molecules. Pertinent information on the amphiphilic character of cellulose and DNA can be obtained from the association with surfactants, as well as on modifying the hydrophobic interactions by additives.
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| 8. |
- Norgren, Magnus, et al.
(författare)
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Aggregation of Lignin Derivatives under Alkaline Conditions. Kinetics and Aggregate Structure
- 2002
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 18:7, s. 2859-2865
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Tidskriftsartikel (refereegranskat)abstract
- The kinetics of kraft lignin (KL) aggregation at alkaline conditions was studied by quasi-elastic light scattering (QELS) and turbidity measurements. Stability ratios (W) for KL were obtained at 70 °C and various concentrations of sodium chloride. By analyzing the early-time evolution data of aggregate growth obtained from QELS, fractal dimensions of flocs formed in both reaction-limited cluster-cluster aggregation regimes and diffusion-limited cluster-cluster aggregation regimes were determined. Correlations between the fractal dimension and the W-ratio were found in accordance to recent studies of a system containing monodisperse polystyrene colloids. By cryogenic transmission electron microscopy, the fractality of KL aggregate structures in the system was also shown. It was seen from stability studies of KL solutions that the effects of specific co- and counterions follow the Hofmeister series. From the outcome of the investigation, different modes of aggregation occurring in a KL system are proposed. Starting from the macromolecular state of KL and evolving through larger aggregates, the KL clusters finally exhibit a supramolecular structure similar to what earlier has been proposed for native softwood lignin.
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| 9. |
- Yang, Jiayi, et al.
(författare)
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Simple one pot preparation of chemical hydrogels from cellulose dissolved in cold LiOH/Urea
- 2020
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Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 12:2
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Tidskriftsartikel (refereegranskat)abstract
- In this work, non-derivatized cellulose pulp was dissolved in a cold alkali solution (LiOH/urea) and chemically cross-linked with methylenebisacrylamide (MBA) to form a robust hydrogel with superior water absorption properties. Different cellulose concentrations (i.e., 2, 3 and 4 wt%) and MBA/glucose molar ratios (i.e., 0.26, 0.53 and 1.05) were tested. The cellulose hydrogel cured at 60 °C for 30 min, with a MBA/glucose molar ratio of 1.05, exhibited the highest water swelling capacity absorbing ca. 220 g H2O/g dry hydrogel. Moreover, the data suggest that the cross-linking occurs via a basic Michael addition mechanism. This innovative procedure based on the direct dissolution of unmodified cellulose in LiOH/urea followed by MBA cross-linking provides a simple and fast approach to prepare chemically cross-linked non-derivatized high-molecular-weight cellulose hydrogels with superior water uptake capacity.
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