| 1. |
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| 2. |
- Agfors, Gunnar, et al.
(författare)
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KEMI : den gränslösa vetenskapen
- 2011
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Bok (populärvet., debatt m.m.)abstract
- Kemi – handlar inte det bara om farliga ämnen och onödiga tillsatser? Det är kanske bildenmånga har av kemi, men faktum är att utan kemi skulle vi inte ha det höga välstånd vi har i dag.Tack vare kemisk kunskap har vi tillgång till läkemedel som botar sjukdomar och lindrar smärta– med hjälp av syntetiska antibiotika kan infektionssjukdomar som tidigare var dödliga botas,magsår kan behandlas utan dyra och plågsamma operationer och många cancerformer kanframgångsrikt behandlas med syntetiska preparat. Konstgödsel och medel som hindrar skadeinsektergör att skördar kan ökas och svälten i världen därigenom begränsas. Tack vare kemin harvi även tillgång till alla de material vi behöver för att tillverka allt från kläder, rengöringsprodukteroch kosmetika till bilar, TV-apparater och reservdelar till kroppen. Det är genom kemisk syntes vikan framställa dessa och alla de övriga produkter vi behöver för vårt dagliga liv och det är keminsom visar vägen till hållbar produktion som utnyttjar förnybara råvaror och ger minimala mängderavfall. Kemisk kunskap är också oumbärlig för utveckling av nanoteknik och medicinskdiagnostik och andra till kemin angränsande områden. Kemin bidrar alltså till att finna lösningartill många av de komplexa globala problem vi står inför: hälsa, klimat, brist på råvaror, utnyttjandetav nya energikällor och tillgång till livsmedel för att föda jordens ökande befolkning. DET ÄR OM ALLT DETTA DEN HÄR BOKEN HANDLAR.
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| 3. |
- Ankerfors, Caroline, et al.
(författare)
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A comparison of polyelectrolyte complexes and multilayers : Their adsorption behaviour and use for enhancing tensile strength of paper
- 2009
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 24:1, s. 77-86
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Tidskriftsartikel (refereegranskat)abstract
- This paper compares the adsorption behaviour and paper-strength-enhancing properties of polyelectrolyte complexes (PECs) and polyelectrolyte multilayers (PEMs) of polyallylamine hydrochloride and polyacrylic acid. Model adsorption experiments using SPAR (stagnation point adsorption reflectometry) and QCM-D (quartz crystal microbalance with dissipation) showed that the amount of complexes adsorbed was lower than the amount adsorbed when forming a multilayer using the same polymer system. From these experiments, in combination with AFM and ESEM imaging, it was concluded that the PEC adsorption stopped before full surface coverage was reached. Tensile testing of handsheets treated with PECs and PEM showed a significant increase in both tensile index and strain-at-break using both systems. The largest strength improvement was achieved with the fibres treated with the largest number of PEMs, but the largest effect per adsorbed amount of polymer was achieved by PEC treatment.
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| 4. |
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| 5. |
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| 6. |
- Ankerfors, Caroline, et al.
(författare)
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Using jet mixing to prepare polyelectrolyte complexes : Complex properties and their interaction with silicon oxide surfaces
- 2010
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 351:1, s. 88-95
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Tidskriftsartikel (refereegranskat)abstract
- The influence of mixing procedure on the properties of polyelectrolyte complexes (PECs) was investigated using two complexation techniques, polyelectrolyte titration and jet mixing, the latter being a new method for PEC preparation. For the low-molecular-weight polyelectrolytes polyacrylic acid (PAA) and polyallyl amine hydrochloride (PAH), shorter mixing times produced smaller PECs, whereas for higher molecular weights of the same polyelectrolytes, PEC size first decreased with decreasing mixing time to a certain level, after which it started increasing again. This pattern was likely due to the diffusion-controlled formation of "pre-complexes", which, in the case of low-molecular-weight polymers, occurs sufficiently quickly to form stable complexes; when polyelectrolytes are larger, however, non-equilibrium pre-complexes, more prone to aggregation, are formed. Comparing the techniques revealed that jet mixing produced smaller complexes, allowing PEC size to be controlled by mixing time, which was not the case with polyelectrolyte titration. Higher polyelectrolyte concentration during jet mixing led to the formation of larger PECs. It was also demonstrated that PEC size could be changed after preparation: increasing the pH of the PEC dispersion led to an irreversible increase in PEC size, whereas lowering the pH did not influence PEC size. The adsorption behavior of PECs formed from weak polyelectrolytes on model substrates was studied using QCM-D, SPAR, and AFM imaging; the results indicated that increasing the pH increased the amount of PECs adsorbed to model surfaces. However, the amount of PECs adsorbed to the model surfaces was low compared with other systems in all studied cases.
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| 7. |
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| 8. |
- Ansari, Farhan, et al.
(författare)
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Hierarchical wood cellulose fiber/epoxy biocomposites : Materials design of fiber porosity and nanostructure
- 2015
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Ingår i: Composites. Part A, Applied science and manufacturing. - : Elsevier BV. - 1359-835X .- 1878-5840. ; 74, s. 60-68
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Tidskriftsartikel (refereegranskat)abstract
- Delignified chemical wood pulp fibers can be designed to have a controlled structure of cellulose fibril aggregates to serve as porous templates in biocomposites with unique properties. The potential of these fibers as reinforcement for an epoxy matrix (EP) was investigated in this work. Networks of porous wood fibers were impregnated with monomeric epoxy and cured. Microscopy images from ultramicrotomed cross sections and tensile fractured surfaces were used to study the distribution of matrix inside and around the fibers - at two different length scales. Mechanical characterization at different relative humidity showed much improved mechanical properties of biocomposites based on epoxy-impregnated fibers and they were rather insensitive to surrounding humidity. Furthermore, the mechanical properties of cellulose-fiber biocomposites were compared with those of cellulose-nanofibril (CNF) composites; strong similarities were found between the two materials. The reasons for this, some limitations and the role of specific surface area of the fiber are discussed.
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| 9. |
- Castro, Daniele Oliveira, et al.
(författare)
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The use of a pilot-scale continuous paper process for fire retardant cellulose-kaolinite nanocomposites
- 2018
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Ingår i: Composites Science And Technology. - : Elsevier Ltd. - 0266-3538 .- 1879-1050. ; 162, s. 215-224
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Tidskriftsartikel (refereegranskat)abstract
- Nanostructured materials are difficult to prepare rapidly and at large scale. Melt-processed polymer-clay nanocomposites are an exception, but the clay content is typically below 5 wt%. An approach for manufacturing of microfibrillated cellulose (MFC)/kaolinite nanocomposites is here demonstrated in pilot-scale by continuous production of hybrid nanopaper structures with thickness of around 100 μm. The colloidal nature of MFC suspensions disintegrated from chemical wood fiber pulp offers the possibility to add kaolinite clay platelet particles of nanoscale thickness. For initial lab scale optimization purposes, nanocomposite processing (dewatering, small particle retention etc) and characterization (mechanical properties, density etc) were investigated using a sheet former (Rapid Köthen). This was followed by a continuous fabrication of composite paper structures using a pilot-scale web former. Nanocomposite morphology was assessed by scanning electron microscopy (SEM). Mechanical properties were measured in uniaxial tension. The fire retardancy was evaluated by cone calorimetry. Inorganic hybrid composites with high content of in-plane oriented nanocellulose, nanoclay and wood fibers were successfully produced at pilot scale. Potential applications include fire retardant paperboard for semi structural applications and as reinforcement mats in molded thermoset biocomposites.
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| 10. |
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| 11. |
- Ciftci, Göksu Cinar, et al.
(författare)
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Tailoring of rheological properties and structural polydispersity effects in microfibrillated cellulose suspensions
- 2020
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Ingår i: Cellulose. - : Springer Science+Business Media B.V.. - 0969-0239 .- 1572-882X. ; 27:16, s. 9227-9241
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Tidskriftsartikel (refereegranskat)abstract
- Abstract: Industrial production of low-charge microfibrillated cellulose (MFC) typically results in wide fibril size distributions. This polydispersity influences viscosity, overall colloidal stability, and rheological properties of MFC suspensions and gels in aqueous systems. In this work, a systematic rheological analysis is performed for industrially prepared MFC and fractions of different size distributions. Gel formation and flow characteristics (e.g., shear-thinning) of each fraction are examined under neutral and acidic conditions and compared with the unfractionated MFC suspension. The effects of size, aspect ratio, and surface charge on the rheology of semi-dilute MFC suspensions are discussed. The results demonstrate that particle size and aspect ratio distribution control the viscoelasticity and shear-thinning properties of MFC suspensions. An increased fraction of small diameter nanofibrils, by ex situ addition of the fine particles with high aspect ratio or removal of the coarsest particles (with lower aspect ratio) by fractionation, significantly enhances the storage modulus and the yield stress of the complex mixture, compared to the properties of the coarser fractions. New insights are also reported on the tailoring of the rheology of highly polydisperse fibrillar mixtures, where the rheological contributions of each fraction are discussed. Graphic abstract: [Figure not available: see fulltext.].
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| 12. |
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| 13. |
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| 14. |
- Enarsson, Lars-Erik, et al.
(författare)
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Adsorption Kinetics of cationic Polyelectrolytes studied with Stagnation Point Adsorption Reflectometry and Quartz Crystal Microgravimetry
- 2008
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 24:14, s. 7329-7337
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Tidskriftsartikel (refereegranskat)abstract
- The effects of charge density, pH, and salt concentration on polyelectrolyte adsorption onto the oxidized surface of silicon wafers were studied using stagnation point adsorption reflectometry and quartz crystal microgravimetry. Five different polyelectrolytes-cationic polyacrylamides of four charge densities and one cationic dextran-were examined. The adsorption kinetics was characterized using each technique, and the adsorption kinetics observed was in line with the impinging jet theory and the theory for one-dimensional diffusion, respectively. The polyelectrolyte adsorption increased with pH as an effect of the increased silica surface charge. A maximum in the saturation adsorption for both types of polyelectrolytes was found at 10 mM NaCl concentration. A significant adsorption also occurred at I M NaCl, which indicated a significant nonionic contribution to the adsorption mechanism. The fraction of solvent in the adsorbed layer was determined to be 70-80% by combining the two analysis techniques. This indicated a loose structure of the adsorbed layer and an extended conformation at the surface, favoring loops and tails. However, considering the solution structure with a hydrodynamic diameter larger than 100 nm for the CPAM and a thickness of the adsorbed layer on the order of 10 nm, the results showed that the adsorption is accompanied by a drastic change in polymer conformation. Furthermore, this conformation change takes place on a time scale far shorter than seconds.
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| 15. |
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| 16. |
- Enarsson, Lars-Erik, et al.
(författare)
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Conformation of preadsorbed Polyelectrolyte Layers on Silica studied by secondary Adsorption of Colloidal Silica
- 2008
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 325:1, s. 84-92
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Tidskriftsartikel (refereegranskat)abstract
- The conformation of cationic polyelectrolytes preadsorbed on macroscopic silica surfaces was studied before and after addition of colloidal silica (CS) and compared to the fixation capacity of CS. The Study included two polyelectrolytes of equal charge density, cationic polyacrylamide and cationic dextran. Adsorbed amounts were determined with stagnation point adsorption reflectometry (SPAR) and quartz crystal microgravimetry (QCM). Unsaturated layers of polyelectrolyte were formed in SPAR by stopping the adsorption at a fractional coverage relative to saturation adsorption. These layers were probed by secondary saturation adsorption of colloidal silica (CS). At low salt concentrations a high fractional coverage of polyelectrolyte was required to attain adsorption of CS, while significant adsorption of CS was found also for low fractional coverages of polyelectrolyte at salt concentrations above 10 mM NaCl. Saturation adsorption of cationic polyacrylamide (CPAM) and cationic dextran (Cdextran) onto the silica surface was found to be similar, while the secondary adsorption of CS was significantly higher onto preadsorbed CPAM compared with Cdextran. The QCM and SPAR data together indicated that the adsorbed layer of Cdextran was thinner than CPAM, and that a loose, expanded layer was formed after adsorption of CS on CPAM but not on Cdextran.
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| 17. |
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| 18. |
- Enarsson, Lars-Erik, et al.
(författare)
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Kinetics of sequential adsorption of polyelectrolyte multilayers on pulp fibres and their effect on paper strength
- 2007
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 22:2, s. 258-266
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Tidskriftsartikel (refereegranskat)abstract
- Conditions for sequential adsorption of polyelectrolyte multilayers (PEM) onto pulp fibres were investigated in terms of appropriate addition levels and adsorption times. The objective was a technical application for improved tensile strength of paper. Two common polyelectrolytes (PE) in papermaking, polyamideamine epichlorolrydrin (PAE) and carboxymethyl cellulose (CMC), were consecutively adsorbed onto long fibres from a bleached softwood kraft pulp, adding up to four PE layers on the fibre surfaces. Adsorption isotherms and adsorption kinetics were studied layer by layer, giving recommended addition levels and adsorption times for each layer. PAE adsorbed in larger amounts than CMC, 4 and 1 mg/g, respectively on fractionated pulp free of fines. For the kinetics, longer times were required to reach saturation adsorption for PAE compared to CMC, corresponding to three and two minutes, respectively. Tensile testing of handsheets based on both fractionated and beaten pulp showed that four PE layers increased the tensile index by about 50%, reaching levels of 34 (unbeaten) and 88 Nm/g (beaten), respectively. The effect of PEM on strain at break depended on the beating level as the fractionated pulp showed an improvement from 2.5 to 4.1% while beaten pulp showed a reduction from 6.1 to 4.5%.
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| 19. |
- Enarsson, Lars-Erik, 1976-
(författare)
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Polyelectrolyte adsorption on oppositely charged surfaces - Conformation and adsorption kinetics
- 2006
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Denna avhandling presenterar experimentella studier av polyelektrolytadsorption på motsatt laddade ytor, där substrat av både kiseloxid och blekt barrsulfatmassa har använts. Ett huvudsakligt syfte med denna forskning var att karaktärisera konformationen hos adsorberade skikt av katjonisk polyakrylamid (CPAM) i jämförelse med katjonisk dextran (Cdextran) och relatera denna information till inbindningskapaciteten av kolloidal kiselsyra. Ett andra syfte i denna avhandling var att studera kinetiken för sekventiell adsorption av polyamidamin epiklorhydrin (PAE) och karboxymetyl cellulosa (CMC) på massafibrer och att bestämma adsorptionsisotermer för deponering av polyelektrolyter skikt för skikt på massafibrer. Adsorptionen av CPAM på kiseloxidytor studeras med stagnationspunkts-reflektometri och kvartskristalls-mikrogravimetri för att bestämma adsorptionskinetiken och mättnadsadsorptionens beroende av polyelektrolytens laddningstäthet, pH och NaCl koncentration. Konformationen hos adsorberade skikt av CPAM och Cdextran bestämdes både före och efter sekundär tillsats av kolloidal kiselsyra (CS) och adsorptionen av CS kvantifierades också som funktion av yttäckningen av polyelektrolyt. Resultaten indikerar att laddningstätheten hos CPAM kontrollerar den adsorberade mängden på kiseloxidytor vid låga NaCl koncentrationer. Både adsorptionen av CPAM och Cdextran på kiseloxid visades vara effektiv i NaCl koncentrationer upp till 1 M, vilket indikerar ett signifikant bidrag av icke-jonisk interaktion mellan polyelektrolyterna och kiseloxid. Adsorptionen av CS var högre på föradsorberad CPAM än Cdextran. Konformationen hos de adsorberade skikten efter tillsats av CS sågs expandera signifikant för skikt baserade på CPAM medan skikt av Cdextran vid låga salthalter verkade återta sin konformation efter en temporär expansion. I den andra delen av avhandlingen studerades sekventiell adsorption av PAE och CMC på massafibrer. Adsorptionsisotermer skikt för skikt på avkryllad massa visade att PAE adsorberade i större mängd än CMC, både i hänseende av massa och laddning. Adsorptionen av PAE var signifikant långsammare än CMC och adsorptionstiden till 90% av mättnadsadsorptionen bestämdes till 3 respektive 1 minut. Zetapotentialen för kryll bestämdes för adsorption av de två första polyelektrolytskikten och resultaten tydde på att kryllmaterialet omladdade inom en minut efter tillsatserna av polyelektrolyt. Reflektometriförsök inom sekventiell adsorption av PAE och CMC på kiseloxid antydde att den låga molekylviktsfraktionen av PAE störde uppbyggnaden av polyelektrolyt-multiskikten.
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| 20. |
- Enarsson, Lars-Erik, et al.
(författare)
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Polyelectrolyte Adsorption on Thin Cellulose Films Studied with Reflectometry and Quartz Crystal Microgravimetry with Dissipation
- 2009
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 10:1, s. 134-141
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Tidskriftsartikel (refereegranskat)abstract
- Thin cellulose films were prepared by dissolving carboxymethylated cellulose fibers in N-methyl morpholine oxide and forming thin films on silicon wafers by spin-coating. The adsorption of cationic polyacrylamides and polydiallyldimethylammonium chloride onto these films was studied by stagnation point adsorption reflectometry (SPAR) and by quartz crystal microgravimetry with dissipation (QCM-D). The polyelectrolyte adsorption was studied by SPAR as a function of salt concentration, and it was found that the adsorption maximum was located at 1 mM NaCl for polyelectrolytes of low charge density and at 10 mM NaCl for polyelectrolytes of high charge density. Electrostatic screening led to complete elimination of the polyelectrolyte adsorption at salt concentrations of 300 mM NaCl. According to the QCM-D analysis, the cellulose films showed a pronounced swelling in water that took several hours to complete. Subsequent adsorption of polyelectrolytes onto the cellulose films led to a release of water from the cellulose, an effect that was substantial for polyelectrolytes of high charge density at low salt concentrations. The total mass change including water could therefore show either an increase or a decrease during adsorption onto the cellulose films, depending on the experimental conditions.
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| 21. |
- Enarsson, Lars-Erik, et al.
(författare)
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Tailoring the chemistry of polyelectrolytes to control their adsorption on cellulosic surfaces
- 2009
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Ingår i: Colloids and Surfaces A. - : Elsevier BV. - 0927-7757 .- 1873-4359. ; 340:1-3, s. 135-142
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption of two types of cationic polyacrylamides in the presence of a background electrolyte was studied on substrates including silicon oxide, kraft pulp fibres and thin films of regenerated cellulose. One of the polyelectrolytes was a conventional cationic polyacrylamide (MeCPAM) and the other was a benzyl-containing derivative of cationic polyacrylamide (BzCPAM). It was found that the aromatic substituents of BzCPAM strongly enhanced the adsorption on substrates of hydrophobically modified silicon oxide when a background electrolyte was present. A similar effect was also seen in the case of BzCPAM adsorption on unbleached pulp fibres, but in this case MeCPAM also exhibited a strong adsorption at high background electrolyte concentrations. On bleached pulp fibres, BzCPAM maintained a high adsorption up to a concentration of 100 mM NaCl whereas MeCPAM adsorption showed a significant decrease at this salt concentration. On model cellulose films, the adsorption of BzCPAM was similar to that of MeCPAM and the non-ionic interactions with cellulose appeared weak, since there was no adsorption of either polyelectrolyte in 300 mM NaCl.
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| 22. |
- Fall, Andreas, et al.
(författare)
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Colloidal Stability of Aqueous Nanofibrillated Cellulose Dispersions
- 2011
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 27:18, s. 11332-11338
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Tidskriftsartikel (refereegranskat)abstract
- Cellulose nanofibrils constitute an attractive raw material for carbon-neutral, biodegradable, nanostructured materials. Aqueous suspensions of these nanofibrils are stabilized by electrostatic repulsion arising from deprotonated carboxyl groups at the fibril surface. In the present work, a new model is developed for predicting colloidal stability by considering deprotonation and electrostatic screening. This model predicts the fibril-fibril interaction potential at a given pH in a given ionic strength environment. Experiments support the model predictions that aggregation is induced by decreasing the pH, thus reducing the surface charge, or by increasing the salt concentration. It is shown that the primary mechanism for aggregation upon the addition of salt is the surface charge reduction through specific interactions of counterions with the deprotonated carboxyl groups, and the screening effect of the salt is of secondary importance.
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| 23. |
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| 24. |
- Hamedi, Mahiar M., et al.
(författare)
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Highly Conducting, Strong Nanocomposites Based on Nanocellulose-Assisted Aqueous Dispersions of Single-Wall Carbon Nanotubes
- 2014
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 8:3, s. 2467-2476
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Tidskriftsartikel (refereegranskat)abstract
- It is challenging to obtain high-quality dispersions of single-wall nanotubes (SWNTs) in composite matrix materials, in order to reach the full potential of mechanical and electronic properties. The most widely used matrix materials are polymers, and the route to achieving high quality dispersions of SWNT is mainly chemical functionalization of the SWNT. This leads to increased cost, a loss of strength and lower conductivity. In addition full potential of colloidal self-assembly cannot be fully exploited in a polymer matrix. This may limit the possibilities for assembly of highly ordered structural nanocomposites. Here we show that nanofibrillated cellulose (NFC) can act as an excellent aqueous dispersion agent for as-prepared SWNTs, making possible low-cost exfoliation and purification of SWNTs with dispersion limits exceeding 40 wt %. The NFC:SWNT dispersion may also offer a cheap and sustainable alternative for molecular self-assembly of advanced composites. We demonstrate semitransparent conductive films, aerogels and anisotropic microscale fibers with nanoscale composite structure. The NFC:SWNT nanopaper shows increased strength at 3 wt % SWNT, reaching a modulus of 133 GPa, and a strength of 307 MPa. The anisotropic microfiber composites have maximum conductivities above 200 S cm(-1) and current densities reaching 1400 A cm(-2).
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| 25. |
- Illergård, Josefin, et al.
(författare)
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Interactions of Hydrophobically Modified Polyvinylamines : Adsorption Behavior at Charged Surfaces and the Formation of Polyelectrolyte Multilayers with Polyacrylic Acid
- 2010
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 2:2, s. 425-433
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Tidskriftsartikel (refereegranskat)abstract
- The structure and adsorption behaviors of two types of hydrophobically modified polyvinylamines (PVAm) containing substituents of hexyl and octyl chains were compared to a native polyvinylamine sample. The conformation of dissolved polyvinylamines was studied in aqueous salt solutions using dynamic light scattering. Modified PVAm showed hydrodynamic diameters similar to native PVAm, which indicated that all PVAm polymers were present as single molecules in solution. The adsorption of the polyvinylamines, both native and hydrophobically modified, from aqueous solution onto negatively charged silica surfaces was studied in situ by reflectometry and quartz crystal microgravimetry with dissipation. Polyelectrolyte multilayers; (PEM) with up to nine individual layers were formed together with poly(acrylic acid). Obtained PEM structures were rigid and showed high adsorbed amounts combined with low dissipation, with similar results for both the modified and unmodified PVAm. This suggests that electrostatics dominated the PEM formation. At lower salt concentrations, the hydrophobically modified PVAm produced multilayers with low water contents, indicating that secondary interactions induced by the hydrophobic constituents can also have a significant influence on the properties of the formed layers. The surface structure of PEMs with nine individual layers was imaged in dry state using atomic force microscopy in a dynamic mode. Modified PVAm was found to induce a different structure of the PEM at 100 mM, with larger aggregates compared to those of native PVAm. From these results, it is proposed that modified PVAm can induce aggregation within the PEM, whereas PVAm remains as single molecules in solution.
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| 26. |
- Joby Kochumalayil, Jose, et al.
(författare)
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Bioinspired and highly oriented clay nanocomposites with a xyloglucan biopolymer matrix : Extending the range of mechanical and barrier properties
- 2013
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 14:1, s. 84-91
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Tidskriftsartikel (refereegranskat)abstract
- The development of clay bionanocomposites requires processing routes with nanostructural control. Moreover, moisture durability is a concern with water-soluble biopolymers. Here, oriented bionanocomposite coatings with strong in-plane orientation of clay platelets are for the first time prepared by continuous water-based processing. Montmorillonite (MTM) and a "new" unmodified biological polymer (xyloglucan (XG)) are combined. The resulting nanocomposites are characterized by FE-SEM, TEM, and XRD. XG adsorption on MTM is measured by quartz crystal microbalance analysis. Mechanical and gas barrier properties are measured, also at high relative humidity. The reinforcement effects are modeled. XG dimensions in composites are estimated using atomistic simulations. The nanostructure shows highly oriented and intercalated clay platelets. The reinforcement efficiency and effects on barrier properties are remarkable and are likely to be due to highly oriented and well-dispersed MTM and strong XG-MTM interactions. Properties are well preserved in humid conditions and the reasons for this are discussed.
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| 27. |
- Karim, Zoheb, et al.
(författare)
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Forming a cellulose based nanopaper using XPM
- 2017
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Ingår i: International Conference on Nanotechnology for Renewable Materials 2017. - : TAPPI Press. - 9781510850897 ; , s. 399-407
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Konferensbidrag (refereegranskat)
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| 28. |
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| 29. |
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| 30. |
- Larsson, Per A., 1980-
(författare)
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Dimensional Stability of Paper : Influence of Fibre-Fibre Joints and Fibre Wall Oxidation
- 2008
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Papper är ett mycket mångsidigt material. Trots detta finns det ett flertal egenskaper som begränsar papperets användbarhet. Ett av de större problemen med cellulosa- och lignocellulosafibrer är att de sänker sin fria energi genom att sorbera vatten, och denna sorption förändrar papperets dimensioner. Detta fenomen kallas vanligtvis för bristfällig dimensionsstabilitet och uppträder i form av registerfel vid flerfärgstryck eller som krullning, buckling och vågiga papperskanter vid utskrift, kopiering och lagring, eller med en vidare definition som förkortad livslängd hos lådor på grund av mekanosorptivt kryp. Avsikten med denna avhandling har varit att studera och kvantifiera vilka egenskaper som styr, och hur de påverkar, den vatteninducerade dimensionsförändringen som sker hos ett fibernätverk, samt hur dess dimensionsstabilitet kan förbättras. Detta har studerats både genom att ändra fiberns fuktsorptionsegenskaper och genom att förändra adhesionen och kontaktgraden mellan fibrerna i fiber-fiberfogarna. Fogegenskaperna har också varierats genom att tillverka laboratorieark torkade under inspänning samt ark torkade fritt för att minimera mängden inbyggda spänningar i arket. Blekt kraftmassa har behandlats med polyelektrolytmultilager (PEM) för att förbättra adhesionen mellan fibrerna och för att öka kontaktgraden mellan fibrerna i fogen. Kontaktgraden har även minskats genom förhorning av fibrerna före arkformning. För de ark som fick torka fritt gav PEM-behandlingen en ökad hygroexpansionskoefficient, det vill säga dimensionsförändringen normaliserad mot förändringen i fuktinnehåll, vid samma förändring i relativ luftfuktighet medan förhorningen minskade hygroexpansionskoefficienten något. Om arken emellertid torkades under inspänning observerades ingen skillnad i hygroexpansionskoefficient mellan de olika fibermodifieringarna. Detta tolkades som ett resultat av en ökad kontaktzon och en större utbredning ut ur fogens plan, när arken torkades utan inspänning. En utbredning som medför att en större del av fiberns transversella expansion överförs som expansion i pappersplanet. Fibrernas fuktsorptionsegenskaper förändrades genom natriumperjodatoxidering av 1,4-glukanernas C2-C3-bindning. Detta skapade sannolikt tvärbindningar i fiberväggen som förbättrade fiberväggens tålighet både genom att låsa fibrillerna närmare varandra och genom att ta bort potentiella adsorptionssäten som annars är tillgängliga för vattenadsorption. Perjodatoxidationen minskar också fibrernas kristallinitet och således frigjorde oxidationen hydroxylgrupper där vattenmolekyler kan adsorbera. Detta innebar att oxidationen både minskade och ökade interaktionen mellan vatten och fibervägg, men dock på olika strukturell nivå. Tvärbindningarna visade sig också märkbart reducera sorptionshastigheten när arken utsattes för en förändrad luftfuktighet så länge de inte tidigare utsatts för relativa luftfuktigheter nära mättnad. Som ett resultat av den lägre förändringen i fuktinnehåll vid en förändring i luftfuktighet från 20 till 85 % RF minskade dimensionsförändringens amplitud för de tvärbundna arken upp till 30 %. Emellertid uppvisade de tvärbundna arken en högre hygroexpansionskoefficeint, vilket innebär att de blev mer känsliga för absoluta förändringar i fuktinnehåll.
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| 31. |
- Larsson, Per A., et al.
(författare)
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Ductile All-Cellulose Nanocomposite Films Fabricated from Core-Shell Structured Cellulose Nanofibrils
- 2014
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 15:6, s. 2218-2223
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Tidskriftsartikel (refereegranskat)abstract
- Cellulosic materials have many desirable properties such as high mechanical strength and low oxygen permeability and will be an important component in a sustainable biomaterial-based society, but unfortunately they often lack the ductility and formability offered by petroleum-based materials. This paper describes the fabrication and characterization of nanocomposite films made of core-shell modified cellulose nanofibrils (CNEs) surrounded by a shell of ductile dialcohol cellulose, created by heterogeneous periodate oxidation followed by borohydride reduction of the native cellulose in the external parts of the individual fibrils. The oxidation with periodate selectively produces dialdehyde cellulose, and the process does not increase the charge density of the material. Yet the modified cellulose fibers could easily be homogenized to CNFs. Prior to film fabrication, the CNF was shown by atomic force microscopy to be 0.5-2 mu m long and 4-10 nm wide. The films were fabricated by filtration, and besides uniaxial tensile testing at different relative humidities, they were characterized by scanning electron microscopy and oxygen permeability. The strength-at-break at 23 degrees C and 50% RH was 175 MPa, and the films could, before rupture, be strained, mainly by plastic deformation, to about 15% and 37% at 50% RH and 90% RH, respectively. This moisture plasticization was further utilized to form a demonstrator consisting of a double-curved structure with a nominal strain of 24% over the curvature. At a relative humidity of 80%, the films still acted as a good oxygen barrier, having an oxygen permeability of 5.5 mL-mu L/(m(2).24 h.kPa). These properties indicate that this new material has a potential for use as a barrier in complex-shaped structures and hence ultimately reduce the need for petroleum-based plastics.
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| 32. |
- Larsson, Per A., 1980-, et al.
(författare)
-
Ductile cellulose nanocomposite films fabricated from nanofibrillated cellulose after partial conversion to dialcohol cellulose
- 2013
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Konferensbidrag (refereegranskat)abstract
- Ductile nanofibrillar nanocomposite films with a strain at break of 18%, and a tensile strength of 185 MPa, have been fabricated from nanofibrillated bleached kraft fibres partially converted to dialcohol cellulose prior to homogenisation. The conversion to dialcohol cellulose was performed by oxidation with sodium periodate to a degree of oxidation of ca. 30%, followed by reduction with sodium borohydride, and the fabricated films consequentially had one stiff cellulose phase and one flexible dialcohol cellulose phase. The liberated nanofibrils were characterised by AFM, after adsorption onto a silica surface, and imaging in tapping mode showed a blend of elementary fibrils with a width of 5 nm and inter-entangled fibril aggregates with a width of 15-20 nm. Besides good mechanical properties, the films also provided good barrier properties; at 0% RH the oxygen permeability was 2 ml·µm/(m2·d·kPa).
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| 33. |
- Larsson, Per A., et al.
(författare)
-
Highly ductile fibres and sheets by core-shell structuring of the cellulose nanofibrils
- 2014
-
Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 21:1, s. 323-333
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Tidskriftsartikel (refereegranskat)abstract
- A greater ductility of cellulosic materials is important if they are to be used in increasingly advanced applications. This study explores the potential for using chemical core-shell structuring on the nanofibril level to alter the mechanical properties of cellulose fibres and sheets made thereof. The structuring was achieved by a selective oxidation of the cellulose C2-C3 bonds with sodium periodate, followed by a reduction of the aldehydes formed with sodium borohydride, i.e. locally transforming cellulose to dialcohol cellulose. The resulting fibres were morphologically characterised and the sheets made of these modified fibres were mechanically tested. These analyses showed a minor decrease in the degree of polymerisation, a significantly reduced cellulose crystal width and a greater ductility. At 27 % conversion of the available C2-C3 bonds, sheets could be strained 11 %, having a stress at break of about 90 MPa, and consequently a remarkable tensile energy absorption at rupture of about 9 kJ/kg, i.e. 3-4 times higher than a strong conventional paper. Zero-span tensile measurements indicated that the treatment increased the ductility not only of sheets but also of individual fibres. This suggests that the amorphous and molecularly more mobile dialcohol cellulose is located as a shell surrounding the crystalline core of the cellulose fibrils, and that, at deformations beyond the yield point, this facilitates plastic deformation both within and between individual fibres.
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| 34. |
- Larsson, Per A., 1980-, et al.
(författare)
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Towards optimised size distribution in commercial microfibrillated cellulose : a fractionation approach
- 2019
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Ingår i: Cellulose. - : Springer. - 0969-0239 .- 1572-882X. ; 26:3, s. 1565-1575
-
Tidskriftsartikel (refereegranskat)abstract
- For the successful commercialisation of microfibrillated cellulose (MFC) it is of utmost importance to carefully characterise the constituent cellulose particles. This could for instance lead to the development of MFC grades with size distributions tailored for specific applications. Characterization of MFC is challenging due to the heterogeneous chemical and structural nature of MFC. This study describes a fractionation approach that combines two steps of physical sieving of larger particles and a final centrifugation step to separate out the smallest, colloidally stable particles, resulting in four distinctly different size fractions. The properties, such as size and charge, of each fraction were studied, as well as MFC filtration time, film formation, and film properties (mechanical and optical). It was found that virtually all surface charges, determined by polyelectrolyte adsorption, are located in the colloidally stable fraction of the MFC. In addition, the amount of available surface charges can be used as an estimate of the degree of fibrillation of the MFC. The partly fibrillated particles frequently displayed a branching, fringed morphology. Mechanical testing of films from the different fractions revealed that the removal of large particles may be more important for strength than achieving full fibrillation. Overall, this study demonstrates that by controlling the size distribution in MFC grades, property profiles including dewatering time to make films by filtration, rheology, film strength and optical transmittance could be optimised. [GRAPHICS] .
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| 35. |
- Li, Lengwan, et al.
(författare)
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Ultrastrong Ionotronic Films Showing Electrochemical Osmotic Actuation
- 2023
-
Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 35:45
-
Tidskriftsartikel (refereegranskat)abstract
- A multifunctional soft material with high ionic and electrical conductivity, combined with high mechanical properties and the ability to change shape can enable bioinspired responsive devices and systems. The incorporation of all these characteristics in a single material is very challenging, as the improvement of one property tends to reduce other properties. Here, a nanocomposite film based on charged, high-aspect-ratio 1D flexible nanocellulose fibrils, and 2D Ti3C2Tx MXene is presented. The self-assembly process results in a stratified structure with the nanoparticles aligned in-plane, providing high ionotronic conductivity and mechanical strength, as well as large water uptake. In hydrogel form with 20 wt% liquid, the electrical conductivity is over 200 S cm−1 and the in-plane tensile strength is close to 100 MPa. This multifunctional performance results from the uniquely layered composite structure at nano- and mesoscales. A new type of electrical soft actuator is assembled where voltage as low as ±1 V resulted in osmotic effects and giant reversible out-of-plane swelling, reaching 85% strain.
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| 36. |
- Lindgren, J., et al.
(författare)
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Charge determinations of cellulose fibres of different origin - Comparison between different methods
- 2002
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 17:1, s. 89-96
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Tidskriftsartikel (refereegranskat)abstract
- Eleven different pulps, both chemically and thermomechanically produced and of both softwood and hardwood origin, were acid/base characterised. The measurements were performed as series of potentiometric and conductometric titrations. The potentiometric titration data revealed that all pulp materials were characterised by two buffer regions with an intervening buffer minimum at pHapproximate to6 and, from these measurements, it was possible to evaluate the buffer capacity in the low pH region. The capacity of the second buffer region could not be quantified since drifting readings characterised the data and since the region extended beyond the area of accurate pH determinations. With the conductometric titration data it was not possible to strictly separate the two buffer regions, and it was concluded that the method, as used in the present work, determined the low pH region buffer capacity plus a minor part of the buffer capacity in the upper buffer region. This conclusion was based on a finding that the differences in buffer capacity, as evaluated with the two methods, was related to the relative amount of the weaker acidity at pH>6. From the potentiometric titration data it was also possible to evaluate additional information, namely the initial charge of the pulps and the thermodynamic acidity of the acidic groups on the fibre. In an attempt to determine the origin of the weaker acidity and to determine the practical importance of this weaker acidity, paper sheets were made from one of the softwood pulps at neutral and alkaline pH and these sheets were spectroscopically and physically characterised.
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| 37. |
- Marais, Andrew, et al.
(författare)
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Pilot-scale papermaking using Layer-by-Layer treated fibres; comparison between the effects of beating and of sequential addition of polymeric additives
- 2016
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 31:2, s. 308-314
-
Tidskriftsartikel (refereegranskat)abstract
- The Layer-by-Layer (LbL) deposition technique was used to treat fibres before papermaking on a pilot scale. Following a laboratory pre-study performed earlier to determine the adsorption isotherms and the kinetics of formation of multilayers of polyamideamine epichlorydrine (PAE) and carboxymethylated cellulose (CMC) on unbeaten, bleached softwood fibres, online LbL treatment of the furnish was carried out on the EuroFEX pilot paper machine. Papers from fibres coated with up to four layers of polyelectrolytes were produced. Two different LbL systems were investigated, with anionic CMC in combination with either PAE or cationic starch (CS). The results showed that the mechanical strength of the paper significantly increased when the fibres were LbL-treated online. A comparison with conventional beating of the fibres revealed that the LbL treatment was a potential substitute to beating treatment, as the density of the LbL-treated papers remained constant while the mechanical properties were significantly improved. At the same time, the press solids content was significantly higher (2%) when using LbL-treated fibres than with beaten fibres.
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| 38. |
- Nordenström, Malin
(författare)
-
Colloidal interactions and arrested dynamics of cellulose nanofibrils
- 2020
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Over the past decades, concerns for the environment have increased and efforts to achieve a sustainable society have intensified. One particular challenge is to replace fossil-based plastics with biodegradable materials produced from renewable resources. Cellulose nanofibril (CNF)-based materials are strong candidates due to their excellent mechanical properties, nano-dimensions and molecular structure, which is suitable for modification. CNFs can be obtained from wood and are elongated, often charged, particles which are usually handled in aqueous dispersions. The colloidal stability is sensitive, and instability results in aggregation or transition to an arrested state. Since the properties of CNF-based materials rely on dispersion of the CNFs, an understanding of the colloidal behaviour is crucial.This work has focused on the interactions and dynamics of CNFs in different colloidal states. Arrested states of CNFs were studied in detail and it was found that two types of arrested state exist, with different colloidal interactions and mechanisms governing their formation. The dynamics in arrested and dispersed states were studied by tracer diffusion measurements, and it was found that small amounts of CNFs can constitute an excellent stabiliser for other particle dispersions according to a so far unexplored mechanism.The effects of altering the colloidal interactions using different strategies were also evaluated. The counterions of CNFs were exchanged and the impact on the swelling behaviour was measured. Based on the results, different contributions to the counterion-dependent interactions are discussed. Two strategies for using polymers to alter the interactions were furthermore studied. Polyethylene glycol (PEG) was grafted to CNFs in order to increase the arrested state threshold concentration. PEG, carboxymethyl cellulose and lignin, were also used as additives which improved the redispersion of dried CNF, especially in the case of samples containing lignin.
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| 39. |
- Nordenström, Malin, et al.
(författare)
-
Colloidal interactions in nanocellulose systems
- 2016
-
Ingår i: Abstracts of Papers of the American Chemical Society. - : AMER CHEMICAL SOC. - 0065-7727. ; 251
-
Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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| 40. |
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| 41. |
- Ondaral, Sedat, et al.
(författare)
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Surface-Induced Rearrangement of Polyelectrolyte Complexes : Influence of Complex Composition on Adsorbed Layer Properties
- 2010
-
Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 26:18, s. 14606-14614
-
Tidskriftsartikel (refereegranskat)abstract
- The adsorption characteristics of two different types of polyelectrolyte complexes (PECs). prepared by mixing poly(allylamine hydrochloride) and poly(acrylic acid) in a confined impinging jet (CIJ) mixer, have been investigated with the aid of stagnation point adsorption reflectometry (SPAR), a quartz crystal microbalance with dissipation (QCM-D), and atomic force microscopy (A FM) using SiO2 surfaces The two sets of PEC were prepared by combining high molecular mass PAH/FAA (PEC-A) and low molt:cubit mass PAH/PAA (PEC-B) The PEC-A showed a higher adsorption to the SiO2 surfaces than the PEC-B The adsorption of the PEC-A also showed a larger change in the dissipation (AD), according to the QCM-D measurements, suggesting that the adsorbed layer of these complexes had a relatively lower viscosity and a lower shear modulus Complementary investigations of the adsorbed layer using A FM imaging showed that the adsorbed layer of PEC-A was significantly different from that of PEC-B and that the changes in properties with adsorption time were very different for the two types of PECs The PEC-A complexes showed a coalescence into larger block of complexes on the SiO2 surface, but this was not detected with the PEC-B The size determinations of the complexes in solution showed that they were very stable over time, and it was therefore concluded that the coalescence of the complexes was induced I the interaction between the complexes and the surface The results also indicated that polyelectrolytes can migrate between the different complexes adsorbed to the surface The results also give indications that the preparation of PEC-B leads to the formation of two different types of polyelectrolyte complexes differing in the amount of polymer in the complexes: i.e., two populations of complexes were formed with similar sizes but with totally different adsorption structures at the solid-liquid interface.
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| 42. |
- Ondaral, Sedat, et al.
(författare)
-
The adsorption of hyperbranched polymers on silicon oxide surfaces
- 2006
-
Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 301:1, s. 32-39
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Tidskriftsartikel (refereegranskat)abstract
- The electrostatic interaction between quarternised hyperbranched polymers (polyesteramides) and a silicon oxide (SiO2) surface has been studied via adsorption studies with quartz crystal microbalance instrument with dissipation (QCM-D). Frequency shift (Delta f) results show that the increase in both pH and salt concentration positively affect the adsorbed amount of these polymers, calculated by Sauerbrey equation, on the QCM crystal. The adsorbed amount of HA1 (with lower molecular weight and higher charge density) was lower than that of HA2 (with higher molecular weight and lower charge density) in all experiments. It was also observed that there are no significant changes in the dissipation after adsorption of these polymers. This indicated that both hyperbranched polymers formed rigid adsorbed layers on the negative SiO2 surface. Additionally, the results were compared with adsorption of poly-DADMAC and the results showed that the hyperbranched polymers formed thicker and more rigid layers as compared with the poly-DADMAC.
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| 43. |
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| 44. |
- Schütz, Christina, et al.
(författare)
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Hard and Transparent Films Formed by Nanocellulose-TiO2 Nanoparticle Hybrids
- 2012
-
Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 7:10, s. e45828-
-
Tidskriftsartikel (refereegranskat)abstract
- The formation of hybrids of nanofibrillated cellulose and titania nanoparticles in aqueous media has been studied. Their transparency and mechanical behavior have been assessed by spectrophotometry and nanoindentation. The results show that limiting the titania nanoparticle concentration below 16 vol% yields homogeneous hybrids with a very high Young's modulus and hardness, of up to 44 GPa and 3.4 GPa, respectively, and an optical transmittance above 80%. Electron microscopy shows that higher nanoparticle contents result in agglomeration and an inhomogeneous hybrid nanostructure with a concomitant reduction of hardness and optical transmittance. Infrared spectroscopy suggests that the nanostructure of the hybrids is controlled by electrostatic adsorption of the titania nanoparticles on the negatively charged nanocellulose surfaces.
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| 45. |
- Walther, Andreas, et al.
(författare)
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Best Practice for Reporting Wet Mechanical Properties of Nanocellulose-Based Materials
- 2020
-
Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 21:6, s. 2536-2540
-
Tidskriftsartikel (refereegranskat)abstract
- Nanocellulose-based materials and nanocomposites show extraordinary mechanical properties with high stiffness, strength, and toughness. Although the last decade has witnessed great progress in understanding the mechanical properties of these materials, a crucial challenge is to identify pathways to introduce high wet strength, which is a critical parameter for commercial applications. Because of the waterborne fabrication methods, nanocellulose-based materials are prone to swelling by both adsorption of moist air or liquid water. Unfortunately, there is currently no best practice on how to take the swelling into account when reporting mechanical properties at different relative humidity or when measuring the mechanical properties of fully hydrated materials. This limits and in parts fully prevents comparisons between different studies. We review current approaches and propose a best practice for measuring and reporting mechanical properties of wet nanocellulose-based materials, highlighting the importance of swelling and the correlation between mechanical properties and volume expansion.
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| 46. |
- Westman, Eva-Helena, et al.
(författare)
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Assessment of Antibacterial Properties of Polyvinylamine (PVAm) with Different Charge Densities and Hydrophobic Modifications
- 2009
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 10:6, s. 1478-1483
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Tidskriftsartikel (refereegranskat)abstract
- Hydrophobically modified and unmodified polyvinylamines (PVAm), including a total of five polymers, were tested against both gram-negative (Escherichia coli) and gram-positive (Bacillus subtilis) bacteria for antimicrobial activity. The assessment of PVAm in solution against bacteria is described, and the influence of the charge density and of the hydrophobic modification of the polyelectrolyte is discussed. The antimicrobial activity was found to depend upon the concentration of PVAm and also on the type of bacteria used. The results also indicated that no direct relationship exists between antimicrobial activity and charge density of the different PVAms. It was, however, observed that an alkyl chain length of six or eight alkane units had a substantial effect on the bacteria investigated. The best combined antibacterial activity for the two bacteria tested was achieved for PVAm with a C-6 alkane substituent (PVAm C-6). To evaluate the antimicrobial activity on a solid substrate, PVAm C-6 was further studied after being deposited onto a glass slide and the results show a large reduction in bacterial infection.
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| 47. |
- Wohlert, Malin, et al.
(författare)
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Cellulose and the role of hydrogen bonds : not in charge of everything
- 2022
-
Ingår i: Cellulose. - : Springer Nature. - 0969-0239 .- 1572-882X. ; 29:1, s. 1-23
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Tidskriftsartikel (refereegranskat)abstract
- In the cellulose scientific community, hydrogen bonding is often used as the explanation for a large variety of phenomena and properties related to cellulose and cellulose based materials. Yet, hydrogen bonding is just one of several molecular interactions and furthermore is both relatively weak and sensitive to the environment. In this review we present a comprehensive examination of the scientific literature in the area, with focus on theory and molecular simulation, and conclude that the relative importance of hydrogen bonding has been, and still is, frequently exaggerated.
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| 48. |
- Wågberg, Lars, et al.
(författare)
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Hyperbranched polymers as a fixing agent for dissolved and colloidal substances on fiber and SIO2 surfaces
- 2007
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Ingår i: Industrial & Engineering Chemistry Research. - : American Chemical Society (ACS). - 0888-5885 .- 1520-5045. ; 46:7, s. 2212-2219
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Tidskriftsartikel (refereegranskat)abstract
- Hyperbranched polymers (polyesteramides) were used as a cationic fixing agent to remove dissolved and colloidal substances (DCS) from the water phase in a fiber suspension. The relative turbidity, electrophoretic mobility, and average diameter of the colloidal particles were determined as a function of polyelectrolyte concentration. The results indicated that maximum removal of DCS was achieved at about zero electrophoretic mobility of the suspension where the negative surface charges of particles were neutralized by the oppositely charged hyperbranched polymer. The amount of hyperbranched polymers needed to maximize DCS fixation on the fibers was higher than the amount of poly-DADMAC (diallyldimethylammonium chloride) needed to reach the same effect. This was found to be due to the lower molecular weight and lower charge density of hyperbranched polymers. The lower molecular mass allowed penetration of these polymers into pores of fibers that resulted in higher polymer consumption before removal of the dissolved and colloidal substances from the fiber suspensions. A lower charge density further resulted in a higher saturation adsorption of the hyperbranched polymer. Experiments with both DCS and model-latex particles showed that the initial increase in relative turbidity was due to the aggregation of particles before fixation to fibers. The results from quartz crystal microbalance with dissipation (QCM-D) experiments showed that the efficiency of hyperbranched polymer and poly-DADMAC was similar even if they had different structure. Therefore, this study highlights the importance of molecular mass and charge density of the polymers as well as the surface structure of polymer layers which in turn gives implications for development of new structures of fixing agents.
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| 49. |
- Åvitsland, G.A., et al.
(författare)
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AKD sizing of TCP and ECF bleached birch pulp characterized by peroxide edge wicking index
- 2006
-
Ingår i: Nordic Pulp and Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 21:2, s. 237-244
-
Tidskriftsartikel (refereegranskat)abstract
- To study the impact of extractable materials and xylan on the sizing efficiency of totally chlorine-free (TCF) bleached birch pulp and elemental-chlorine-free (ECF) bleached birch pulp, several pulps with different amounts of extractable material were studied. The content of extractable material in the pulp was shown to be detrimental for sizing efficiency, measured both as Cobb60 values and edge penetration in a model liquid packaging board, and a higher content of extractable material causes a reduced sizing efficiency for a given pulp. No significant difference was observed between extracted TCF and ECF bleached birch pulps, while unextracted pulps containing the same amount of extractable material yielded different sizing efficiencies. The TCF bleached birch pulp had a lower sizing efficiency than did the ECF bleached birch, probably because of differences in the fatty acid composition. A greater amount of extractable material also resulted in a smaller fraction of non-extractable alkyl ketene dimers (AKD) relative to the total amount of AKD in the sheet. Enzymatic removal of xylan and thus the reduction of the surface charge had no measurable effect on sizing efficiency. Extracted TCF and ECF bleached pulps only need a content of 0.05 kg/ton non-extractable AKD or 0.08 kg/ton total AKD in the sheets produced to achieve a good sizing effect.
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| 50. |
- Åvitsland, Grete, et al.
(författare)
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AKD sizing of TCF and ECF bleached birch pulp characterized by peroxide edge wicking
- 2006
-
Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 21:2, s. 237-241
-
Tidskriftsartikel (refereegranskat)abstract
- To study the impact of extractable materials and xylan on the sizing efficiency of totally chlorine-free (TCF) bleached birch pulp and elemental-chlorine-free (ECF) bleached birch pulp, several pulps with different amounts of extractable material were studied. The content of extractable material in the pulp was shown to be detrimental for sizing efficiency, measured both as Cobb. values and edge penetration in a model liquid packaging board, and a higher content of extractable material causes a reduced sizing efficiency for a given pulp. No significant difference was observed between extracted TCF and ECF bleached birch pulps, while unextracted pulps containing the same amount of extractable material yielded different sizing efficiencies. The TCF bleached birch pulp had a lower sizing efficiency than did the ECF bleached birch, probably because of differences in the fatty acid composition. A greater amount of extractable material also resulted in a smaller fraction of non-extractable alkyl ketene dimers (AKD) relative to the total amount of AKD in the sheet. Enzymatic removal of xylan and thus the reduction of the surface charge had no measurable effect on sizing efficiency. Extracted TCF and ECF bleached pulps only need a content of 0.05 kg/ton non-extractable AKD or 0.08 kg/ton total AKD in the sheets produced to achieve a good sizing effect.
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