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Hornification, a complex phenomenon occurring during drying of lignocellulosic materials because of formation of irreversible chemical bonds, remains a subject of scientific interest. This study aims to shed light on the underlying mechanisms of hornification by investigating interactions between the liquid and solid phases through a solvent exchange treatment. The treatment involved replacing water with various solvents in suspensions of never-dried cellulose samples, including alcohols (methanol, ethanol, isopropanol) capable of forming hydrogen bonds, albeit to a lesser extent than water, as well as non-alcohol solvents (acetone, ethyl acetate, toluene, heptane) that do not possess the ability to form chain of hydrogen bond, and no hydrogen bond between each other. The impact of solvents on the hornification process was evaluated using WRV measurements. Our findings reveal that water, as a solvent, plays a dominant role in the hornification process, primarily due to its excellent capability to form bridges of hydrogen bonds. In comparison, hornification with alcohols was considerably lower than with water, likely attributed to the smaller ability of alcohols to engage in such interactions. Furthermore, our results indicate a tendency for reduced hornification also when using non-hydrogen bond solvents with decreased polarity. This strengthens the hypothesis related to chains of hydrogen bonds. Additionally, the interaction between hydrophobic surfaces on cellulose through hydrophobic interactions could provide another plausible explanation.

In the pulp and paper industry, pulp testing is typically a labor-intensive process performed on hand-made laboratory sheets. Online quality control by automated image analysis and machine learning (ML) could provide a consistent, fast and cost-efficient alternative. In this study, four different supervised ML techniques—Lasso regression, support vector machine (SVM), feed-forward neural networks (FFNN), and recurrent neural networks (RNN)—were applied to fiber data obtained from fiber suspension micrographs analyzed by two separate image analysis software. With the built-in software of a commercial fiber analyzer optimized for speed, the maximum accuracy of 81% was achieved using the FFNN algorithm with Yeo–Johnson preprocessing. With an in-house algorithm adapted for ML by an extended set of particle attributes, a maximum accuracy of 96% was achieved with Lasso regression. A parameter capturing the average intensity of the particle in the micrograph, only available from the latter software, has a particularly strong predictive capability. The high accuracy and sensitivity of the ML results indicate that such a strategy could be very useful for quality control of fiber dispersions.

There is an ever-increasing demand for renewable, recyclable and biodegradable packaging solutions,from consumers, producers of goods, and producers ofpackaging materials. Closing the material loop andincreasing recyclability of fiber-based package materials isone of the keys to move forward towards a more sustainablefuture. While the recyclability rates of fiber-based packagingare high, packaging boards with high wet-strength can poseproblems due to problems with repulping. This manuscriptinvestigated the possibilities to reduce the use of polyamideepichlorohydrin resins (PAE) by supporting the processsystem with carboxy-methylated cellulose (CMC) throughmachine trials in mill scale production. The focus of theinvestigation was on the wet-strength of the board productand the repulpability value. The results given from thefull-scale trial were positive, indicating a potential in usingCMC while reducing the PAE addition. The results showedthat wet tear strength and wet tensile strength of the boardwere maintained, while higher repulpability rates weregiven, encouraging better recyclability of the board material. This will be beneficial to the environment both withlower use of non-renewable chemicals and possibilities forhigher degrees of recycling of the board products.

The development of sustainable and renewable materials is paramount in today’s society. As the most abundant biopolymer on Earth, cellulose from cellulose-rich fibres is an excellent alternative for advanced and innovative material solutions. Nonetheless, competing with the impressive material properties and the low manufacturing costs of fossil-based plastics imposes great challenges. To increase the potential of cellulose fibres in a broader set of applications, the material properties of cellulose need to be tuned depending on the application. An in-depth study of the fibre structure and the application of different tailoring techniques is required to induce tailoring of the physical and chemical properties of the cellulose fibre materials. This thesis focuses on the structure-property relationship of fibrillar hydrogel networks as model structures for the delignified wet-fibre wall. First, a mathematical framework was developed to describe the characteristics of the swelling and mechanical behaviour of anisotropic fibrillar structures, considering the fibril aspect ratio, surface chemistry of the fibrils, and electrolyte concentration in the system. A chemical functionalisation was then introduced to the fibrillar structure, which provided the CNFs with colloidal stability and the ability to participate in free radical polymerisation with monomers and telechelic oligomers. As a result, fibrillar networks were crosslinked with flexible polymer links that provided the network with different mechanical and chemical properties. Additionally, by tailoring the molecular weight of the crosslinks, the ionic strength of the solution, and even the aspect ratio of the fibrils, the mechanical properties of the network were tuned to be either stiffer or more ductile. Finally, an innovative and more sustainable approach was developed to introduce charge and alkene functionality to the fibres. Following the lessons learned from the CNF model investigations, a polymerisation, Utvecklingen av hållbara och förnyelsebara material är avgörande i dagens samhälle. Eftersom cellulosa ifrån växtfibrer är den mest förekommande biopolymeren på jorden är den ett utmärkt alternativ för användning i avancerade och innovativa materiallösningar. Det innebär dock en enorm utmaning att konkurrera med de imponerande materialegenskaperna och låga tillverkningskostnaderna hos fossilbaserade plaster. För att utnyttja den inneboende potentialen hos cellulosafibrerna och utveckla deras egenskapsrymd för användning i vidare tillämpningar är det helt nödvändigt att modifiera cellulosans materialegenskaper för att passa till specifika slutanvändningar. Det är därför nödvändigt att ingående studera hur olika modifieringstekniker kan användas för att skräddarsy fysikaliska och kemiska egenskaper hos cellulosan på olika strukturella nivåer i de delignifierade fibrerna. Arbetet i denna avhandling har fokuserats på att klarlägga struktur-egenskapsförhållandena för cellulosa-rika fibrilstrukturer. Initialt användes fibrillära hydrogelnätverk som modell för den delignifierade våtfibreväggen. Till att börja med utvecklades ett matematiskt ramverk för att beskriva det typiska svällningsbeteendet och de mekaniska egenskaperna hos de anisotropa fibrillstrukturerna med avseende på fibrillernas längs/tvärs förhållande, ytkemi och elektrolytkoncentration i systemet. Efter detta modifierades fibrillerna på ett sådant sätt att de erhöll en god kolloidal stabilitet samtidigt som de försågs med en vinyl-funktionalitet som innebar att de kunde användas i friradikalpolymerisation med olika typer av monomerer och telecheliska oligomerer. Via denna typ av radikalpolymerisation var det möjligt att skapa fibrillnätverk med flexibla polymerkopplingar som resulterade i skräddarsydda mekaniska och kemiska egenskaper. Genom att kontrollera tvärbindningarnas molekylvikt, lösningens jonstyrka och fibrillernas längs/tvärs förhållande kunde nätverkets mekaniska egenskaper kontrolleras så att, QC 20240118Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2024-01-16

The electrification and digitalization of our society has propelled the demand for energy storage solutions. High-end technologies have been developed to satisfy the requirements of demanding applications, such as electromobility and portable consumer electronics, which also increasingly find markets for less demanding applications. These markets include grid and domestic energy storage, as well as Internet of Things (IoT). However, using high-end technologies for low-end applications is a waste of resources that puts unnecessary stress on the supply lines. Thus, more low-cost cost and environmentally friendly alternative technologies are sought, among which renewable biobased materials derived from agriculture and forestry play a prominent role. The dominant chemical constituents in plants, cellulose and lignin, exhibit some intriguing electrochemical and colloidal properties. Cellulose has been found to efficiently stabilize various electronic materials, whereas lignin can be used as an electronic material itself. Lignocellulosic materials also open for papermaking as an alternative manufacturing approach. Taking the step to using papermaking methods is, however, a bit far from the technology readiness level, as the vast majority of the research on paper electrodes is based on nanocellulose. The material properties of such nanopapers are indeed extraordinary, but the lack of large-scale production methods for nanopapers is a serious challenge. To circumvent this obstacle and find a shortcut to the realization of paper electrodes, this thesis has turned to conventional papermaking techniques. Fibres are essentially different to nanofibrils by their difference in size, and the papermaking process requires careful composition of the formulations. Thus, as the research on nanopaper electrodes cannot be directly translated into conventional papermaking techniques, this calls for separate studies on fibre-based systems. This thesis is based on four separate works carrie

Kraft pulping of wood is based on efficient depolymerization and solubilization of lignin, while cellulose is relatively undamaged. Non-cellulose cell wall polysaccharides are however in some cases heavily degraded, especially pectin and to a lesser degree also glucomannan while, xylan is relatively stable. In this mini-review, the most important reactions in lignin and polysaccharide degradation in kraft pulping are described, both the technically favorable and the problematic reactions, and the chemical background to discuss the advantages and drawbacks of the process. An attempt to put the different reactions in the perspective of the goals of the pulping process is made and a special focus is on the development of color in the pulp fiber during the kraft pulping.

This manuscript presents the study of water absorption by paperboard subjected to water at high hydrostatic pressure based on a modified Cobb tester. The new tester is based on TAPPI Standard Test Method T 441; however, the water column can reach up to 550 mm. The evaluation consisted of measurements of water absorption for coated and uncoated paperboard at different exposure times from 5 s to 45 s and water column heights from 10 mm to 500 mm (corresponding to hydrostatic pressures 98 Pa and 4.9 kPa, respectively). The coatings were formulated as a combination of styrene acrylate (SA; two binder levels) and two types of ground calcium carbonates (differing particle sizes) to form the two pre -coating structures: open and closed. The coating weight was 6 g/m2 applied on 210 g/m2 solid bleached board (SBB). In addition, 210 g/m2 uncoated boards were studied. Characterization of the coatings was performed with scanning electron microscopy (SEM), mercury intrusion, and roughness. It was found that the new device properly mimics the conditions of the current Cobb tester. The characterization of the coating also confirmed the presence of more open/larger pores of open coatings, confirming the desired coating structure. The absorption of boards was mainly driven by exposure pressure by comparing with exposure time. This was already evident after shorter periods of exposure time at 5 s and also 15 s exposure time. Paperboards with open coatings showed slightly higher absorption than other boards.

Fundamental research plays a pivotal role in the development of sustainable solutions that benefit both our environment and everyday lives. Cellulose, as an abundant and renewable resource, holds immense potential for sustainable applications. However, navigating the complexities of molecular and supramolecular structure of cellulose poses significant challenges in harnessing its full potential. By delving into fundamental research, we aim to uncover the underlying mechanisms governing cellulose interactions, paving the way for innovative advancements in sustainable material development.This thesis uncovers the intricate relationship between fundamental research and applied methodologies by showing how molecular contact and structure at the interface of cellulose-rich materials will control the development of the macroscopic mechanical properties of networks from cellulose-rich fibres. The study encompasses various facets, ranging from the development of model materials for studying interfacial interactions to the preparation of fibrous networks with tailored properties.In the initial part of the work the research delves into the development of model materials to investigate interactions at smooth interfaces of regenerated cellulose. The study reveals the crucial role of the making and breaking of cellulose interface, or sometimes interphase, in the development of adhesive joints. Experimental findings demonstrate how chemical additives influence the interactions between cellulose surfaces, thereby modulating the structural and adhesive properties at the interface. Furthermore, by utilizing model materials, insights are gained into fibre-fibre interactions and the influence of surface treatments on network formation and mechanical performance. Lastly, the research focused on investigating the preparation of fibrous networks at different densities and amount of adsorbed additives, providing a comprehensive understanding of how network density and composition affect m, Grundläggande forskning spelar naturligtvis en avgörande roll i utvecklingen av hållbara materiallösningar och processer som gynnar både vår miljö och vårt vardagsliv. Cellulosa, som är en förnyelsebar och rikligt tillgänglig råvara, har också en enorm användnings potential i olika typer av hållbara material. Cellulosan har dock en avancerad och komplicerad molekylär och över molekylärstruktur och det är därför svårt att till fullo utnyttja den inneboende potentialen hos denna fascinerande råvara. Genom att fördjupa oss i och klarlägga de molekylära mekanismer som ligger till grund för växelverkan mellan cellulosarika ytor har vi skapat en grundförutsättning för att kunna utnyttja cellulosans inneboende egenskaper i olika typer av fiberbaserade nätverk . Resultaten i avhandlingen understryker den komplicerade och användbara kopplingen som finns mellan grundläggande förståelse och praktiska tillämpningar genom att visa hur den molekylära kontakten och strukturen i gränsytan mellan två cellulosa-rika ytor kommer att kontrollera de makroskopiska egenskaperna hos nätverk ifrån cellulosa rika fibrer. Studierna i avhandlingen omfattar olika aspekter, allt ifrån utvecklingen av väldefinierade och nm-jämna modellmaterial, för att studera molekylära växelverkai gränsytan mellan två cellulosa ytor, till framställningen av fibrösa nätverk med skräddarsydda egenskaper.I den första delen av arbetet har fokus legat på att utveckla väl karakteriserade modellmaterial och väldefinierade metoder för att klarlägga växelverkan i gränsytan eller gränsfasen mellan två cellulosa ytor. Resultaten visar också hur tillsats kemikalier påverkar växelverkan mellan cellulosa ytor och hur valet av kemikalier kan användas för att styra de strukturella och adhesiva egenskaperna hos gränsytan. Genom att använda våra modellmaterial har det också varit möjligt att bättre förstå de grundläggande mekanismerna som kontrollerar fiber-fiberväxelverkningar och därigenom hur tillsatskemikalier eller fibermod, QC 2024-04-08

Nanocellulose, originated from cellulose, the primary structural component of the cell walls of plants, has garnered significant attention for its excellent mechanical, optical, and barrier properties, as well as its renewable and sustainable nature. Various forms of nanocellulose, including cellulose nanocrystals and cellulose nanofibers (CNFs), are produced by breaking down lignocellulosic fibers into nanoscale dimensions, typically through mechanical or chemical processes. The large surface area and rich hydroxyl groups of CNFs are ideal for surface modifications, offering great versatility in the development of functional biocomposite materials. This thesis aims to design CNF-based composites with integrated multifunctionalities, including redispersibility, biocompatibility, mechanical robustness, wet integrity, as well as optical transparency, through surface engineering of cellulose nanofibers. The methodology involves strategically selecting CNFs, integrating CNFs with biopolymers, applying surface modifications, and implementing facile processing techniques. In Paper I, inspiration from plant cell wall was drawn to customize the interaction between water and CNFs. By Incorporating mixed-linkage beta-glucan from barley, superior rehydration, redispersion, and recycling of dried CNFs have been achieved. This advancement holds the potential to enhance the transportation and processability of CNF-based materials. In Paper II, by leveraging the interaction between CNF and water, a facile material processing technique was introduced to fabricate CNF/regenerated silk fibroin (RSF) composites. This involved rehydration and swelling of TEMPO-oxidized CNF nanopaper structures with both random-oriented CNF and nematic-ordered CNF in the RSF solutions. Remarkably, the CNF/RSF composite films thus prepared exhibited exceptional mechanical properties in both dry conditions and in PBS, and demonstrated excellent biocompatibility when cultured with L929 fibroblast cell. In, Nanocellulosa, som ursprungligen kommer från cellulosa, den primära strukturella komponenten i växters cellväggar, har fått betydande uppmärksamhet för sina unika egenskaper, inklusive utmärkta mekaniska, optiska och barriäregenskaper, samt dess förnybara och hållbara natur. Nanocellulosa, inklusive cellulosa nanokristaller och cellulosa nanofibrer (CNF), produceras genom att bryta ned lignocellulosa fibrer till nanoskala dimensioner, vanligtvis genom mekaniska eller kemiska processer. Den stora ytan och de rika hydroxylgrupperna hos CNF är idealiska för ytmodifieringar, vilket avsevärt ökar dess mångsidighet i utvecklingen av funktionella biokompositmaterial. Denna avhandling syftar till att designa CNF-baserade kompositer med integrerade multifunktionaliteter inklusive redispergerbarhet, biokompatibilitet, mekanisk robusthet, våtintegritet, samt optisk transparens genom ytmodifiering av cellulosananofibrer. Metodiken innefattar strategiskt val av CNF, integrering av CNF med biopolymerer, tillämpning av ytmodifieringar och implementering av enkla bearbetningstekniker. I Paper I inspirerades man av växtcellväggen för att anpassa interaktionen mellan vatten och CNF. Genom att tillsätta betaglukan från korn, har bättre rehydrering, redispersion, och återvinning av torkade CNF uppnåtts. Denna framsteg möjliggör förbättring av transporten och bearbetningen av CNF-baserade material. I Paper II, utnyttjades interaktionen mellan CNF och vatten, vilket introducerade en enkel materialbearbetningsteknik för att tillverka CNF/regenererad silkfibroin (RSF) kompositer. Detta involverade rehydrering och svullnad av TEMPO-oxiderade CNF nanopapperstrukturer med både slumpmässigt orienterade CNF och nematiskt ordnade CNF i RSF-lösningarna. De förberedda CNF/RSF kompositfilmerna uppvisade exceptionella mekaniska egenskaper både i torra förhållanden och i PBS, och visade utmärkt biokompatibilitet när de odlades med L929 fibroblastcell. I Paper III, förbereddes CNF/alginate dubbelnätve, QC 20240404Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2024-04-04

Cellulose-based aerogels are emerging bio-based materials for a range of applications in the quest toward a circular and carbon-neutral society. Owing to their lightweight nature, high porosity, high specific surface area, biocompatibility, and biodegradability, cellulose aerogels are suitable for packaging, insulation, wound care products, hygiene products, and water purification. However, their commercial use is hampered by complicated time- and energy-consuming fabrication processes. Hence, industrially relevant processes with upscaling opportunities need to be developed for cellulose-based aerogels to reach their full potential. This thesis explores different scalable and simple methods for preparing and designing highly porous aerogels with high wet integrity using cellulose-rich fibers and cellulose nanofibrils (CNFs). As wet integrity is crucial for specific applications and enables further functionalization of the aerogels using water-based chemistry, different methods were developed to achieve wet integrity without complicated crosslinking procedures. The effects of the raw materials and processing methods on the final material properties were also carefully studied to optimize the performance for the targeted applications. Moreover, the role of the network-forming ability of CNFs in the development of functional materials with structural integrity was explored by incorporating small amounts of CNFs in aerogel systems based on macroscopic cellulose-rich fibers and nanosized metal-organic frameworks. Finally, the potential of the different developed cellulose-based or cellulose-reinforced aerogels with high wet integrity was demonstrated in applications for which the aerogels’ structural integrity and physical and mechanical properties are highly advantageous, such as biomedical applications, gas storage and separation, flame retardancy, and hygiene products. As demonstrated in this thesis, these functional aerogel materials could be a bio-based alternativ, Cellulosabaserade aerogeler har på senare tid visat sig vara användbara biobaserade material för olika tillämpningar i strävan mot ett cirkulärt och kolneutralt samhälle. Materialens mycket låga densitet, höga porositet, höga specifika yta, biokompatibilitet och biologiska nedbrytbarhet innebär att cellulosaaerogeler är lämpliga för förpackningar, isolering, sårvårdsprodukter, hygienprodukter och vattenrening. Den kommersiella användningen har dock bromsats av komplicerade, tid- och energikrävande tillverkningsmetoder. Därmed måste industriellt relevanta processer med uppskalningsmöjligheter utvecklas för att cellulosabaserade aerogeler ska nå sin fulla potential. Denna avhandling utforskar olika skalbara och enkla metoder för att bereda och skräddarsy högporösa och våtstabila aerogeler från cellulosafibrer och cellulosananofibriller (CNFer). Eftersom våtstabilitet är avgörande för vissa tillämpningar och möjliggör ytterligare funktionalisering med vattenbaserad kemi, har ett omfattande arbete genomförts för att identifiera nya metoder för att skapa en god våtstabilitet utan att använda komplicerade tvärbindningsprocedurer. Ett stort fokus har även lagts på att klarlägga råvarans och bearbetningsmetodernas inverkan på de slutliga materialegenskaperna för att optimera prestandan för riktade tillämpningar. Dessutom har CNFers unika nätverksbildande egenskaper också utforskats i att skapa funktionella material med strukturell integritet från mycket små mängder CNFer i aerogelsystem baserade på makroskopiska cellulosarika fibrer och nanopartiklar av metallorganiska nätverk. Slutligen demonstrerades potentialen av de framställda cellulosabaserade och cellulosaförstärkta aerogelerna med utmärkt våtstyrka i tillämpningar där deras strukturella integritet, fysikaliska och mekaniska egenskaper kan användas på ett mycket fördelaktigt sätt, till exempel biomedicinska applikationer, gaslagring och -separering, flamskydd, och hygienprodukter. Mot bakgrund av dessa resultat är d, QC 20240522Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2024-05-14

Expanding our understanding of how cellulose fibers and fibrils interact with water and its effect on their inherent properties is needed to optimize their utilization in the making of novel bio-based materials, but also useful in more traditional products (pulp, paper, and packaging). The overall objective of the work in this thesis was to deepen the understanding of drying-induced structural changes and cellulose-water interactions using cellulosic model materials. Cellulose nanofibrils (CNFs) were employed as they present a distinct advantage with their defined geometry and controlled surface chemistry compared to macroscopic cellulose fibers. The first part considers the fundamental interactions of CNFs in contact with water and by water removal, and is devoted to identifying the molecular mechanisms behind the process known as hornification. This was done by studying the exposure of CNF sheets to different heat treatments to establish a connection between their reswelling properties, chemical and structural characteristics, and mechanical behavior. The findings indicate that hornification is governed by non-covalent interactions and that the diffusion of water back into a hornified CNF network is kinetically limited. Furthermore, the influence of fibril aspect ratio and chemical functionality on the mechanical properties of wet fibrillar networks was studied. Fibrils were prepared from fibers with different hemicellulose content. It was found that longer fibrils formed stiffer and more ductile materials, owing to a longer-range and more uniform distribution of stress transfer. Additionally, high aspect ratio fibrils form networks capable of holding larger amounts of water. It was also possible to elucidate the influence of aspect ratio on the network formation, where long and short fibrils form networks with different topologies. These results were integrated into a mechanical network model to present an improved elastoplastic description of the network propert, Att utvidga vår förståelse för hur cellulosafibrer och fibriller interagerar med vatten och dess effekt på deras inneboende egenskaper är nödvändigt för att optimera deras användning vid tillverkning av nya biobaserade material, men även i traditionella produkter (massa, papper och förpackningar). Det övergripande målet med arbetet i denna avhandling var att fördjupa förståelsen för strukturella förändringar orsakade av torkning och cellulosa-vatten interaktioner med hjälp av cellulosabaserade modellmaterial. Cellulosa nanofibriller (CNFs) användes då de har en fördel med sin definierade geometri och kontrollerade ytkemi i jämförelse med makroskopiska cellulosafibrer. Den första delen avhandlar de grundläggande interaktionerna mellan CNFs i kontakt med vatten och efter vattenborttagning, och ägnas åt att identifiera de molekylära mekanismerna bakom processen som kallas hornifiering. Detta gjordes genom att studera CNF-ark som utsatts för olika värmebehandlingar för att fastställa en koppling mellan deras svällningsegenskaper, kemiska och strukturella egenskaper samt mekaniska beteende. Resultaten indikerar att förhorning styrs av icke-kovalenta interaktioner och att diffusionen av vatten tillbaka in i ett förhornat CNF-nätverk är kinetiskt begränsad. Sedan studerades inflytandet av fibrillernas längd-bredd förhållande och kemisk funktionalitet på de mekaniska egenskaperna hos våta fibrillnätverk. Fibriller framställdes från fibrer med olika hemicellulosahalt. Resultaten visade att längre fibriller bildade styvare och mer töjbara material, tack vare en längre och mer jämn fördelning av belastningsöverföring. Dessutom bildar fibriller med högt längd-bredd förhållande nätverk som kan hålla större mängder vatten. Det var också möjligt att förklara inflytandet av längd-bredd förhållande på nätverksbildningen, där långa och korta fibriller bildar nätverk med olika topologier. Dessa resultat integrerades i en mekanisk nätverksmodell för att presentera en förbättrad elasto, QC 20240508Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2024-05-08

Long, slender cellulose nanofibrils (CNF) are unique with their high axial modulus, small diameter, high flexibility, and the possibility of chemical tailoring of, among other things, their surface charge density. The objective of this work has been to elucidate how the hydrogel network properties and how their related deformation mechanisms depend on CNF properties, concentration, and chemical environment. In addition, the influence of CNF characteristics on the formation of the structure and properties of isotropic hydrogels, anisotropic hydrogels, and aerogels has been studied. This was done by combining theoretical models describing the CNF network's topology and mechanics with high-resolution experiments to validate the theoretical models. Furthermore, the properties of the fibrils have been characterized in detail and linked to the material properties of materials formed from the fibrils. Finally, the CNF networks in this work have been functionalized in two different ways. In the first case, a flow channel was created within the hydrogel network at extremely low CNF concentrations, that could be surface treated with a Layer-by-layer (LbL) methodology with a consecutive addition of oppositely charged polyelectrolytes/nanoparticles to add new functionalities to the channels. Secondly, wet stable aerogels, prepared at higher concentrations of CNFs, were treated using the LbL methodology to adjust the aerogels' surface structure and surface energy, thereby controlling the liquid spreading rate properties of the formed networks. The most important findings in this work are that CNF network topology and network mechanics can be described using theoretical, rather non-complicated, elastoplastic models. Furthermore, at lower concentrations of CNFs, the network structure is formed in a more organized way, meaning that the fibrils have the time and freedom to seek their optimal contact points during the network formation from a thermodynamic free energy point of view., Långa, smala cellulosananofibriller (CNF) är unika med sin höga axiella E-modul, låga diameter, höga flexibilitet och stora möjlighet till kemisk modifiering som bland annat använts för att styra fibrillernas ytladdningstäthet. Syftet med detta arbete har varit att klarlägga hur egenskaperna hos hydrogeler, framställda av nanofibriller, och dess deformationsmekanismer, kan kopplas till olika grundläggande CNF-egenskaper, koncentration och kemisk miljö. Dessutom har vi studerat inverkan av hur CNF-egenskaperna påverkar den bildade nätverksstrukturen och hur de påverkar de slutliga egenskaperna hos isotropa- och anisotropa hydrogeler och aerogeler som formats ifrån de olika fibrillslagen. Den strategi som användes, och visade sig mycket framgångsrik, för att nå dessa mål, var att kombinera teoretiska modeller som beskriver CNF-nätverkets topologi och mekanik med specialdesignade experiment för att validera de teoretiska modellerna. Vidare har ett omfattande arbete lagts ned på att karakterisera fibrillernas kemiska, strukturella och morfologiska egenskaper och att koppla dessa till de funktionella materialegenskaperna hos de material som har tillverkats ifrån dessa fibriller. Slutligen har de färdiga CNF-nätverken funktionaliserats på två olika sätt. I det första fallet skapades en stabil flödeskanal i ett hydrogelnätverk, som preparerats vid extremt låg CNF-koncentration, och det visade sig vara möjligt att ytbehandla denna kanal med en lager för lager (LbL) metod där motladdade polyelektrolyter och/eller nanopartiklar användes för att tillföra nya egenskaper till kanalen. I det andra fallet behandlades förtillverkade, våtstabila aerogeler, som preparerats vid högre koncentration av CNF, med en LbL-behandling för att kontrollera ytstruktur och ytkemi hos aerogelerna, och att därigenom kontrollera vätskespridningshastigheten hos nätverken. De viktigaste resultaten i detta arbete är att CNF-nätverkets topologi och nätverksmekanik kan beskrivas med hjälp av relativt ok, QC 2024-04-30Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2024-04-18.

Paper-based materials, such as paperboard, are commonly used as packaging materials. In addition to the fact that paper is renewable, there are also many other benefits of paperboard. From a mechanical point of view, paperboard has a high bending stiffness compared to its relatively low weight and high foldability, which are properties of significance in the design of packages. However, a distinct drawback of paperboard is its significant sensitivity to moisture. The moisture reduces the mechanical properties of the paperboard and consequently reduces the performance of the package. This thesis addresses the impact of paperboard deformation and damage mechanisms on packaging performance, with the characterization of the material properties as a starting point. Initially, the relations between moisture and different mechanical properties on a continuum material level were investigated. Then, experimental testing and finite element (FE) simulations were applied to evaluate these relations at the packaging design level. In Paper A, a material characterization was performed on five commercial paperboards with different basis weights, from the same producer. Five types of mechanical tests to characterize the paperboards material properties were performed: In-plane tensile test, Out-of-plane tensile test, Short-span Compression Test (SCT), Two-point folding, Double-notch shear test. All tests were performed at several levels of relative humidity (RH). Linear relations between the mechanical properties normalized with their respective value at 50 % RH and moisture ratio were found. Paper B examined whether the linear relationships discovered in Paper A are also valid for other paperboard series. Therefore, this study investigated 15 paperboards from four producers at the same RH levels as in Paper A. The paperboards were chosen to be different in furnish and construction, where four recycled boards were included. Here, the in-plane stiffnesses, strengths and SCT values we, Kartong är ett exempel på ett vanligt, pappersbaserat, förpackningsmaterial. Utöver från att det är återvinningsbart så finns det även andra fördelar med att använda kartong i förpackningar. Ur ett mekaniskt perspektiv har exempelvis kartong hög böjstyvhet i förhållande till sin vikt samt är enkelt att vika, vilket är två betydelsefulla egenskaper vid förpackningsdesign. En uppenbar nackdel med kartong däremot, är dess känslighet för fukt, som försämrar de mekaniska egenskaperna hos kartongmaterialet och således även förpackningsprestandan. Med materialkaraktärisering som utgångspunkt, tar den här avhandlingen upp deformationer och skademekanismers påverkan på kartongförpackningars prestanda. Initialt avhandlas relationen mellan fukt och olika mekaniska egenskaper hos kartongmaterialet på kontinuumnivå. Därefter lyfts dessa relationer upp på förpackningsnivå, genom experimentell förpackningsprovning och datorsimuleringar med finita elementmetoden (FEM). I Artikel A genomfördes en materialkaraktärisering på fem kommersiella kartonger från samma producent, men med olika ytvikt. Följande provmetoder användes vid materialkaraktäriseringen: Dragprov (i planet), Dragprov (ut ur planet), Korta kompressionsprov (SCT), Böjstyvhetsprov, Skjuvprofilsprov. Samtliga prov utfördes vid flera olika nivåer av relativ fuktighet (RH). Linjära relationer mellan mekanisk egenskap normerad med motsvarande värde vid 50 % RH och fukt noterades. Artikel B utvärderade huruvida de linjära samband som noterades i Artikel A gäller för andra kartongserier. Således användes totalt 15 kartongkvalitéer från fyra olika tillverkare. Provningen skedde under samma förhållanden som i Artikel A. Kartongerna valdes noga ut för att säkerställa att de hade olika konstruktion och innehåll. Exempelvis innehöll fyra av kartongerna endast återvunna fibrer. Artikel B avgränsades till att endast utvärdera dragprov i planet, samt SCT som funktion av fukt. Till skillnad från Artikel A så normerades även fuktkvotern, QC 230227

Sustainability has gained a lot of attention in the field of research. Researchers and consumers both prioritize sustainability and environmental issues over previously dominant materials, such as plastic. Packaging and disposable items that used to be made of plastic have largely been replaced with paper. Unfortunately, paper does not perform as well as plastic regarding barrier properties against grease, oxygen, or water vapor. Barrier properties are an important factor when choosing packaging material for food, among other things, as they help maintain the shelf life of the product. In order to improve the properties of the paper packaging and expand its use, the paper is coated with a polymer. However, the polymer contributes to challenges in the recycling of the products as some of the polymer attaches to the fibers, causing difficulties in the separation of each material. Small fragments of plastic may end up in the material streams and the recycled pulp due to the existing challenges in completely removing plastic from cellulosic substrates during recycling. This thesis analyzes the possibilities of identifying and classifying plastic fragments of polyethylene (PE) and polyvinyl alcohol (PVOH) in recycled paper sheets using near-infrared spectroscopy together with multivariate data analysis. The purpose of the work is to develop models that can identify possible residues that may appear in recycled products from various industries. Paper sheets of two different grammages and six different compositions of recycled fiber and virgin fiber were created and scanned by NIR, with and without plastic film under the sheets. The scans were used to develop classification models to identify and categorize scans not included in the calibration data set. The performance of the models was tested by applying them to images of sheets of paper with plastic fragments of different sizes and different type underneath. The results indicated potential in the method. The prediction

We are provided countless products from the forest industry and has been through many years. Paper, paper board, packaging materials and furniture to mention a few. A special type of paper used in food packaging for example, is greaseproof paper. Many producers of greaseproof papers use the toxic and harmful group of chemicals called per- and polyfluorinated alkyl substances (PFAS) in coating since they possess grease resistance. Nordic Paper is a manufacturer of iamKraft® kraft paper and greaseproof paper with over a hundred years of experience without the use of PFAS. Without PFAS, they instead rely on excess refining to form a very dense paper. Nordic Paper has decided to introduce the addition of eucalyptus fibers to the softwood sulfate pulp to enhance the formation of the paper. This study aims to investigate the effects of ~20% addition of eucalyptus fibers to softwood sulfate pulp in regard to refiner energy expended, air permeance (as a measure of grease resistance) and formation. Laboratory work has been done on hand made sheets with a vacuum suction box in laboratory scale. Eight different pulps (four with addition of eucalyptus), provided from Nordic Paper Seffle AB, Säffle, with different refining degree was used in this study. The vacuum pressure used was 20 kPa through all tests, with dwell times 0, 1, 2.5, 5, 10, and 20 ms on sheets with a grammage of 50 g/m2. The study has shown that the pulp with ~20% addition of eucalyptus achieved 86°SR with only 82% expended energy relative to the softwood pulp, which had a refining degree of 87°SR. This small difference in refining degree led to a similar development in dewatering after 20 ms dwell time and 20 kPa, where the softwood pulp achieved a dryness of 9.2% and the pulp with addition of eucalyptus achieved 9.0% dryness. The formation of the softwood pulp was worse, which was the reason for the implementation of addition of eucalyptus. The air permeance on the other hand was not improved by the eucalyptu, Vi tillhandahåller otaliga produkter från skogsindustrin och har gjort i många år. Papper, kartong, förpackningsmaterial och möbler för att nämna några. En speciell typ av papper som används i till exempel livsmedelsförpackningar är fettresistent papper. Många tillverkare av dessa papper använder den giftiga och skadliga gruppen av kemikalier som kallas per- och polyfluorerade alkylämnen (PFAS) i beläggning eftersom de har fettbeständiga egenskaper. Nordic Paper är en tillverkare av iamKraft® kraftpapper och ”greaseproofpapper” med över hundra års erfarenhet utan användning av PFAS. Utan PFAS förlitar de sig istället på extra malning av fibrer för att bilda ett mycket tätt papper. Nordic Paper har beslutat att införa tillsats av eukalyptusfibrer till sulfatmassa av barrved för att förbättra formationen på papperet. Denna studie syftar till att undersöka effekterna av ~20 % tillsats av eukalyptusfibrer till barrsvedssulfatmassan med avseende på förbrukad malningsenergi, luftpermeans (som ett mått på fettbeständighet) och formation. Laborationer har utförts på handgjorda ark med vakuumsuglåda i laboratorieskala. Åtta olika massor (fyra med tillsats av eukalyptus), tillhandahållna från Nordic Paper Seffle AB, Säffle, med olika malningsgrad användes i denna studie. Vakuumtrycket som användes var 20 kPa genom alla tester, med uppehållstider 0, 1, 2.5, 5, 10 och 20 ms på ark med en ytvikt på 50 g/m2. Studien har visat att massan med ~20% tillsats av eukalyptus uppnådde 86°SR med endast 82% förbrukad energi i förhållande till sulfatmassan, som hade en malningsgrad på 87°SR. Denna lilla skillnad i malningsgrad ledde till en liknande utveckling i avvattning efter 20 ms uppehållstid och 20 kPa, där sulfatmassan uppnådde en torrhalt på 9.2% och massan med tillsats av eukalyptus uppnådde 9.0% torrhalt. Formationen på sulfatmassan var sämre, vilket var anledningen till genomförandet av tillsats av eukalyptus. Luftpermeansen å andra sidan förbättrades inte av eukalyptusen, men me

Följande studie syftar till att kartlägga planeringsprocessen och identifiera brister med den, samt ge förbättringsåtgärder för omrullningen på ett fallföretag. Genom utvecklingen av en generell konceptuell modell för att förbättra planeringsprocesser av omrullning. Under alla år har efterbehandlingsprocessen varit nedprioriterad på fallföretaget, och därmed också planeringsprocessen av den. Vid produktion av papper sker, som i många industrier, ett oväntat utfall av produkter som fått defekter under tillverkningen. Produkterna som har defekter kan oftast räddas och säljas genom att efterbehandlas, och en av dessa efterbehandlingar kallas omrullning. Att undersöka och förstå processer inom företag är avgörande för att göra förbättringar. Studien presenterar förbättringsförslag som baserats på de brister som identifierades med planeringsprocessen. Förslagen innefattar bland annat att skapa ett effektivare IT-system, etablera tydliga kommunikationsvägar och öka engagemanget från ledningen. Dessa insatser kan öka effektiviteten, minska slöseri och bättre tillgodose kundernas behov, vilket ökar konkurrenskraften och lönsamheten inom pappersindustrin. Företaget kan implementera detta förbättringsarbete genom att tillsammans analysera och bryta ner målbilden till mindre små mål som går att uppnå på kort sikt. Baserat på insamlade data presenterar studien en konceptuell modell för att analysera och förbättra planeringsprocessen för omrullning. Förslag på vidare studier har getts, där det kan undersökas samma process på flera företag för att se om samma problematik finns där. Det är också vidare forskning att på fler företag använda den framtagna modellen för att analysera och förbättra planeringsprocesser för efterbehandling för att öka generaliserbarheten., The following study aims to map the planning process and identify deficiencies within it, as well as provide improvement measures for the rewinding process in a case company. By developing a general conceptual model to enhance rerolling planning processes. Over the years, post-processing operations have been overseen, including the planning process associated with them. In paper production, like in many industries, defective products are generated during manufacturing. These defective products can often be salvaged and sold through post-processing, with one such process being rewinding. Examining and understanding processes within companies is crucial for making improvements. This study aims to map the planning process of rewinding and develop a conceptual model to enhance post-processing planning. The study presents improvement suggestions based on the deficiencies identified in the planning process. The suggestions include creating a more efficient IT system, establishing clear communication channels, and increasing management involvement. These efforts can enhance efficiency, reduce waste, better meet customer needs, thereby increasing competitiveness and profitability within the paper industry. The company can implement these improvement efforts by collectively analyzing and breaking down the target vision into smaller short-term goals that can be achieved. Based on the collected data, the study presents a conceptual model for analyzing and improving the rerolling planning process. Suggestions for further studies have been provided, where the same process can be examined in multiple companies to determine if similar issues exist. Additionally, further research can be conducted in more companies using the developed model to analyze and improve post-processing planning processes, aiming to increase generalizability.

Carbon fibers (CF) are a material with a composition of over 90% carbon, which has high mechanical properties and low density. This unique combination of properties makes it requirable in applications such as vehicles, aerospace, wind power, and space industries. Commercially made CF are made using the fossil raw material polyacrylonitrile (PAN). In order to make a more sustainable precursor fiber (PF), this project has focused on other raw materials; cellulose and lignin. The PFs were produced with a cellulose and lignin mixture (70:30 wt%). In order to make a more green production of PF, cold alkali system was used as the solution in conjunction with wet spinning with an acid:salt coagulation bath. The acid:salt baths used was the P system with phosphoric acid and ammonium dihydrogen phosphate (ADHP), and the S system with sulphuric acid and sodium sulphate with varying concentrations of both acid and salt. The objectives for this thesis was to evaluate the effect of the acid:salt coagulation bath composition, as well as the spin finish. This was done using tensile tests where Young’s modulus, strain to failure, and tensile strength (TS) were determined. The spin finish was evaluated using thermogravimetric analysis (TGA). The results showed that the P system had a significantly higher Youngs modulus and tensile strength compared to the S system, whilst the S system had a higher strain to failure. For the different concentrations of the S system, the tensile tests showed no significant difference between the concentrations. The fibers contained more phosphorus when ADHP was added to the spin finish, making them more flame retardant.

Munksunds pappersbruk är ett integrerat massa- och pappersbruk som består av två fiberlinjer, en barr- och en lövlinje där båda kokarna är kontinuerliga med efterföljande tvättsteg. En kartering av COD (eng. Chemical Oxygen Demand) och natrium utfördes för båda linjerna för att utvärdera tvätteffektiviteten. COD anger hur mycket syre som krävs för att bryta ned det kvarvarande organiska materialet och natrium används som en indikator på tvättförlusten av kokkemikalierna. Karteringen utfördes genom att analysera in- och utgående flöden vid varje tvättsteg, exklusive kokarna. En förenklad metod användes, där tre flöden analyserades och den fjärde beräknades genom flödes- och massbalanser. Modellen som användes för att beskriva tvätteffektiviteten för respektive utrustning var tvättutbytet Y, som erhölls genom en massbalans. Studien visade att halten COD och Natrium minskar mest från början för respektive linje och når ett gränsvärde runt 8,2 kg COD/adt och 6,6 kg Na/adt för barrlinjen, respektive 8,5 kg COD/adt och 4,8 kg Na/adt för lövlinjen, där ytterligare substans inte kan tvättas bort. Båda linjerna tvättar likvärt med avseende på COD, men lövlinjen tvättar bättre med avseende på natrium. I det sista tvättsteget hade båda fiberlinjerna eliminerat 98% av den inkommande COD-mängden med massan från kokarna. Vidare hade barrlinjen eliminerat 86% och lövlinjen 93% med avseende på natrium i det sista tvättsteget. Utvärderingen av de olika tvättutrustningarna visade att DD-filtret i lövlinjen var effektivast både med avseende på COD och natrium, följt av PO-pressen. På barrlinjen var filter 1 mest effektivt med avseende på COD och natrium., A mapping of COD (Chemical oxygen demand) and sodium will be done to evaluate the different washing steps. COD describe the amount of oxygen needed to dissolve the organic matter left in the pulp and sodium is used as an indicator of the washing loss of the cooking chemicals. The in- and outgoing streams of the washing steps was analyzed to examine the efficiency. A simplified method was applied where three streams were analyzed and the fourth was calculated through flow-and mass balances. The model used to describe the wash efficiency in this study was the wash yield, which can be obtained by mass balances. The study showed that the content of COD and sodium decreased most in the beginning and reaches a limit value of 8,2 kg COD/adt and 6,6 kg Na/adt in the softwood pulp line and 8,5 kg COD/adt and 4,8 kg Na/adt in the soft wood pulp line, where no more content could be removed. Both pulp lines washed efficient with aspect of COD, but the hardwood pulp line washed more efficient in the aspect of natrium compared to the softwood pulp line. In the last washing step, both pulp lines had removed 98% of the ingoing COD from the digester. With aspect to natrium the softwood pulp line had removed 86% and the hardwood pulp line 93% in the last washing step. The evaluation of the different washing equipment showed that the DD-filter in the hardwood pulp line was the most efficient with aspect of both COD and Sodium, followed by the PO-press. In the softwood pulp line, filter 2 was the most efficient regarding both COD and Sodium. The flow- and mass balances turned out to be complicated at some of the washing steps, especially around the Q1-press in the hardwood pulp line and press 1-3 and filter 2 in the softwood pulp line. The reason for this could be that different functional chemicals are added before the Q1-press, which was not considered in this study, additional causes could be unidentified flows that affect the balances. The study was limited to only analyze three st

The environmental concerns that come with the currently used traditional papermaking process where petroleum-based additives are used, has tempted researchers to study “green” additives by introducing environmentally friendly modifications of cellulose as an additive in the papermaking process. This thesis will spin further on that by producing additives with different charge densities and focus on to incorporate an etherification reaction into potentially greens systems based on non-toxic and readily biodegradable deep eutectic solvent (DES). Before modifying the cellulose with DES, an oxidation of cellulose to dialdehyde cellulose (DAC) with sodium periodate as oxidizing agent, took place. The high reactivity of the aldehyde groups in DAC serves as a starting material for further derivatization. The aldehyde content (AC) in the DAC was measured using titration. Additionally, the charge densities (mmol/g) of all modified pulps were determined by using a particle charge detector. The dewatering and drainage abilities of the different modified pulps was determined by measuring the drainage (°SR), the moisture ratio (g/g) before and after vacuum dewatering, and the water retention value (g/g). The tensile strength index was tested on the paper sheets and all parameters were compared with a reference pulp to find out which ionic DES was the most effective in modifying cellulose and using it as a wet-strength additive. From the result gained, one can see that there is a correlation between charge density and mechanical strength as well as the fibres capability to retain water. Generally, swelling considerably improves the strength properties of paper meanwhile the additives with strength-enhancing effects are also the additives that decrease the dewatering capacity. The conclusions from this work are that DESs reagents can work as sustainable modification methods for increasing the mechanical strength of papers together with oxidation of cellulose. In particular the ca

Polymers are often combined with magnetostrictive materials to enhance their toughness. This study reports a cellulose nanofibril (CNF)-based composite paper containing dispersed CoFe2O4 particles (CNF-CoFe2O4). Besides imparting magnetization and magnetostriction, the incorporation of CoFe2O4 particles decreased the ultimate tensile strength and increased the fracture elongation of the CNF-CoFe2O4 composite paper. CNF was responsible for the tensile properties of CNF-CoFe2O4 composite paper. Consequently, the magnetic and magnetostrictive properties and tensile properties of CNF-CoFe2O4 composite paper can be controlled by changing the mixture ratio of CNF and CoFe2O4 particles.

Kraft pulping is more than one hundred years old. The kraft lignin recovery has however been implemented commercially in the last ten years. The lignin is a bio-based by-product and is thus considered a sustainable material with a great potential. These aspects have sparked intense research and development efforts to valorize kraft lignin. This Opinion provides a snapshot of the current state of affairs in the field, highlighting recent examples that either manipulate the kraft lignin to thermoset materials or depolymerize the lignin to obtain biofuels., QC 20230227

If cellulosic materials are to replace materials derived from non-renewable resources, it is necessary to overcome intrinsic limitations such as fragility, permeability to gases, susceptibility to water vapour and poor three-dimensional shaping. Novel properties or the enhancement of existing properties are required to expand the applications of cellulosic materials and will create new market opportunities. Here we have overcome the well-known restrictions that impede melt-processing of high cellulose content composites. Cellulose fibres, partially derivatised to dialcohol cellulose, have been used to manufacture three-dimensional high-density materials by conventional melt processing techniques, with or without the addition of a thermoplastic polymer. This work demonstrates the use of melt processable chemically modified cellulose fibres in the preparation of a new generation of highly sustainable materials with tuneable properties that can be tailored for specific applications requiring complex three-dimensional parts., QC 20230227

Nanoscale infrared (IR) spectroscopy and microscopy, enabling the acquisition of IR spectra and images with a lateral resolution of 20 nm, is employed to chemically characterize individual cellulose nanocrystals (CNCs) and cellulose nanofibrils (CNFs) to elucidate if the CNCs and CNFs consist of alternating crystalline and amorphous domains along the CNF/CNC. The high lateral resolution enables studies of the nanoscale morphology at different domains of the CNFs/CNCs: flat segments, kinks, twisted areas, and end points. The types of nano-cellulose investigated are CNFs from tunicate, CNCs from cotton, and anionic and cationic wood-derived CNFs. All nano-FTIR spectra acquired from the different samples and different domains of the individual nanocellulose particles resemble a spectrum of crystalline cellulose, suggesting that the non-crystalline cellulose signal observed in macroscopic measurements of nanocellulose most likely originate from cellulose chains present at the surface of the nanocellulose particles., QC 20230109

The ability of cationized dialdehyde cellulose to improve the mechanical properties of paper was evaluated. The majority of cationized additives are synthesized by introducing cationic groups through chemical reactions. Here, cationized additives were produced in a more environmentally friendly manner by use of non-toxic and readily biodegradable deep eutectic-like solvent mixtures (DESs). The modified cellulose’s properties were characterized by FTIR, polarized-light optical microscopy, charge titrations, and SEM/EDX. The cationized additives were investigated as strength additives for papermaking. Three different amounts of cationic additive (2%, 5%, and 10%) were added to the pulp, and the properties of handsheets were studied. Because increasing the additive content can affect dewatering of the process, the dewatering capabilities of the pulps with additives were evaluated by Schopper-Riegler (°SR) value, water retention value (WRV), and vacuum dewatering. Finally, the recyclability of the DES was assessed in terms of cationization reaction efficiency and their effect on paper mechanical properties.

Syfte och avgränsningar Studiens syfte har varit att ta fram effektiviseringslösningar kopplat till lager- ochutlastningshanteringen genom att ta fram automatiseringslösningar. Studien har avgränsat sigtill lager- och utlastningshanteringen och inte tagit hänsyn till andra delar i värdeflödet. Fokushar varit lagringen av massabalar men författaren anser att resultaten är tillämpningsbara iandra lager också. Metod Studiens grund ligger i att vara en undersökande studie där tidigare forskningen står förramverket. Primärdata samlades in genom kvalitativa semistrukturerade intervjuer medindivider i olika befattningar för att erhålla en helhetsförståelse av automatiseringens effekter.Intervjuerna analyserades med hjälp av tematisk analys, kompletterad av innehållsanalys. Resultat och analys Studiens resultat lyfter vikten av förståelse om behoven vid automatisering för att undvikaöverdrivet komplexa och kostsamma system. För att automatisera i tung industri anses detbästa alternativet vara traverskranar då den klarar storleken på produkterna. Studien belyserde effekter en automatisering skulle medföra för beslutsfattande. Genomförandet avförändringar kan en viss form av motstånd förväntas, vilket behöver hanteras genom olikametoder såsom att kartlägga och bedöma omfattningen av motståndet.

Kraft lignin, a by-product from the production of pulp, is currently incinerated in the recovery boiler during the chemical recovery cycle, generating valuable bioenergy and recycling inorganic chemicals to the pulping process operation. Removing lignin from the black liquor or its gasification lowers the recovery boiler load enabling increased pulp production. During the past ten years, lignin separation technologies have emerged and the interest of the research community to valorize this underutilized resource has been invigorated. The aim of this Review is to give (1) a dedicated overview of the kraft process with a focus on the lignin, (2) an overview of applications that are being developed, and (3) a techno-economic and life cycle asseeements of value chains from black liquor to different products. Overall, it is anticipated that this effort will inspire further work for developing and using kraft lignin as a commodity raw material for new applications undeniably promoting pivotal global sustainability concerns.

Nanocellulose has a wide range of applications in the field of functional materials, and it has piqued the interest of researchers for some time. This is because nanocellulose inherits the advantages of environmental friendliness and easy availability of plant cell walls in nature, as well as the unique morphology of nanostructures. This review presents four types of nanocellulose including cellulose nanocrystals (CNCs), cellulose nanofibrils (CNFs), regenerated nanocellulose (RNC) and bacterial cellulose (BC), introduces the different preparation routes and their mechanisms, analyzes the advantages and drawbacks between these approaches, and summarizes the potential applications in the field of functional materials such as reinforced composite materials, biomedical materials, soft templates, and optical materials. Finally, future development directions are proposed including further enrichment of nanocellulose raw materials, improvement of preparation methods to adapt to more diversified raw materials, and classification of products according to their morphology and properties to improve the use efficiency.

Fire retardants, although can impart fire-safety in polymeric composites, are detrimental to the mechanical properties. Biochar can be used, in conjunction with fire retardants, to create a balance between fire-safety and mechanical performance. It is possible to thermally dope fire retardants into the pores of biochar to make it functionalised. Thus, the current work is intended in identifying a composite having the combination of the most desirable fire retardant, bioplastic, and a suitable processing method. A comparison was made between two fire retardants (lanosol and ammonium polyphosphate), bioplastics (wheat gluten and polyamide 11), and composite processing methods (compression and injection moulding). It was found that wheat gluten containing ammonium polyphosphate-doped biochar made by compression moulding had the best fire-safety properties with the lowest peak heat release rate (186 kW/m2), the highest fire performance index (0.6 m2s/kW), and the lowest fire growth index (1.6 kW/ms) with acceptable mechanical properties compared to the corresponding neat bioplastic. Thus, for gluten-based polymers, the use of ammonium polyphosphate thermally doped into biochar processed by compression moulding is recommended to both simultaneously improve fire-safety and conserve the mechanical strength of the resulting biocomposites., Validerad;2023;Nivå 2;2023-06-13 (hanlid)

Polyester dendrimers based on 2,2 bis(hydroxymethyl)propionic acid have been reported to be degradable, non-toxic, and exhibit good antimicrobial activity when decorated with cationic charges. However, these systems exhibit rapid depolymerization, from the outer layer inwards in physiological neutral pHs, which potentially restricts their use in biomedical applications. In this study, we present a new generation of amine functional bis-MPA polyester dendrimers with increased hydrolytic stability as well as antibacterial activity for Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa) planktonic bacteria strains. These new derivatives show generally good cytocompatibility for the concentrations they are active toward bacteria, in monocyte/macrophage-like cells (Raw 264.7), and human dermal fibroblasts. Fluoride - promoted esterification chemistry, anhydride chemistry, and click reactions were utilized to produce a library from generations 1–3 and with cationic peripheral groups ranging from 6 to 24 groups, respectively. The dendrimers were successfully purified using conventional purification techniques as well as characterized by matrix-assisted laser desorption ionization time-of-flight mass spectroscopy, nuclear magnetic resonance, and size exclusion chromatography. As proof of synthetic versatility, dendritic-linear-dendritic block copolymer were successfully synthesized to display cysteamine peripheral functionalities as well as the scaffolding ability with biomedically relevant lipoic acid and methoxy polyethylene glycol., QC 20230526

A cohesive interface model based on a master curve is proposed for the analysis of delamination in paperboard under various loading, unloading, and reloading conditions. The model is thermodynamically consistent and considers the effects of elasticity, plasticity, and damage. The proposed model is verified by comparing its predictions with experimental data obtained from multiple loading–unloading–reloading cycle experiments using a split double cantilever beam specimen. The results show that the model can predict the cyclic behavior of shear loading and provide insight into the damage evolution associated with different loading paths by analyzing the shear stress distribution in the fracture process zone. The model’s calibration process requires monotonic normal and shear loading data but only cyclic normal loading data. Additionally, the model accounts for the paperboard’s fiber–fiber friction and normal dilatation due to shear loading. In total, nine parameters are needed to calibrate the mode.

Screening of pulp can be expressed as a process where solid contaminants are removed from a pulp slurry without an excessive loss of fibres of acceptable quality. The impurities originate from the feedstock, or they are generated during the transport, handling, storage, or pulping process. The most typical impurities include bark, fibre bundles or shives, knots, plastic, rubber, and sand. Moreover, there are also other objectives for screening, such as the improvement of the pulp quality, savings in bleaching chemical consumption, and protection of process equipment. In industrial applications, pulp screening is typically carried out with more than one screen for a more beneficial screening result. The pulp screening equipment can be divided into different types by the separation technique employed, such as atmospheric or pressurized screens, centrifugal screens, vibrating screens, etc. In addition, there are other types of related equipment that are common in the pulp screening process, such as knotters, refiners, and hydrocyclones. The main objective of this review is to discuss the advantages and disadvantages of modern screening equipment as well as introduce contemporary screening strategies for chemical pulp mills.

Wood-based panels are indispensable in many areas, such as the construction industry and furniture production. The intensified demand for renewable materials, rising wood prices and increasing protection zones of forest areas make the wood panel industry consider alternative raw materials. The agricultural sector provides, at the same time, large amounts of sustainable and renewable lignocellulosic materials. By-products can arise along the entire agricultural production chain, i.e., during harvesting or further processing into food, but their potential has not yet been fully exploited. This thesis explored the potential of agro-industry feedstocks and side streams as raw materials for wood panel manufacturing. A literature review on the research of agricultural residues as a raw material in wood panels provided an overview of the investigated wood alternatives and their performance in final products. Most of the studies focused on the production of particleboard and its mechanical and physical properties. Often only up to 30% of wood could be replaced by alternative raw materials before the properties decreased remarkably.This thesis focused on an intensive material characterisation of barley husks (BH), oat husks (OH) and wheat bran (WB). Husks are the protective surrounding of their cereal grain and have an anatomical leaf structure. Wheat bran is a side stream of flour production and consists of the grain's outer layers. It was found that BH and OH have at 70% and 66% a slightly lower holocellulose content than wooden materials (poplar, spruce), while their hemicelluloses content exceeding that of cellulose. Additionally, WB had a very high lignin content of 43%. The chemical composition, especially the ash content (5% BH, 6% OH) and the high silicon occurrence on the husks’surfaces, reduced their wettability, as demonstrated by low contact angle measurements. Micromechanical tests showed that OH could resist a higher ultimate stress load than BH and WB, but the

Antimicrobial resistance (AMR) is one of the major global threats to thehealth of humans, animals, plants and ecosystems. AMR arises whenbacteria, viruses, fungi, and parasites undergo changes over time; makingmedicines such as antibiotics, antivirals, antifungals and antiparasiticineffective at treating infections. In 2014, it caused approximately 700 000deaths worldwide which increased to 1.27 million deaths in 2019.Consequently, there is a need to explore novel technologies andtreatments. Within the development of alternatives to conventional smallmoleculeantibiotics, polycationic macromolecules have emerged, such asdendritic polymers and their nanomaterials.Dendrimers are high precision, branched macromolecules with a highdensity of terminal functional groups. Their unique architecture and abilityfor precise control over both shape and surface functionality make themsuitable for biomedical applications such as drug delivery, gene deliveryand antimicrobials.Cellulose nanofibrils (CNFs) are nanoscale fibrils of cellulose, an abundantpolymer typically derived from wood. The prolonged reliance on fossilbasedproducts is associated with a wide range of adverse environmentalconsequences which have prompted the exploration of raw materialsderived from renewable resources. The intriguing properties of CNFs, suchas high elastic moduli and low densities, have made them attractive asstructural materials from sustainable sources that can form 3D networks.The combination of cationic dendritic polymers and cellulose nanofibrils isexplored in this thesis and presents an exciting avenue for the developmentof innovative biomaterials with antibacterial properties andbiocompatibility. Part of the work focuses on the synthesis of cationicdendritic polymers, with varying types of cationic groups at the peripheralthrough the use of fluoride-promoted esterification chemistry and thioleneclick reactions. Another part focuses on creating crosslinked hybridhydrogels using cationic dendrim, Antimikrobiell resistens (AMR) är ett av dem stora globala hoten motmänniskors, djurs, växters och ekosystemens hälsa. AMR uppstår närbakterier, virus, svampar och parasiter genomgår förändringar över tid,vilket gör läkemedel som antibiotika, antivirala, svampdödande ochantiparasitära medel ineffektiva vid behandling av infektioner. År 2014orsakade AMR ungefär 700 000 dödsfall över hela världen och siffranökade till 1,27 miljoner under 2019. Därför finns det ett behov av attutforska nya teknologier och behandlingar. Inom utvecklingen avalternativ till konventionella småmolekylära antibiotika harpolykatjoniska makromolekyler såsom dendritiska polymerer framträtt.Dendrimerer är kraftigt förgrenade makromolekyler och perfektdefinierade med en hög densitet av funktionella grupper. Deras unikaarkitektur gör dem intressanta för biomedicinska applikationer somfrisättning av läkemedel och antimikrobiella material.Cellulosa nanofibriller (CNF) är fibriller av cellulosa med en diameter inanoskala, en polymer som vanligtvis utvinns från trä. Det långvarigaberoendet av fossilbaserade produkter har resulterat i allvarligamiljökonsekvenser, vilket har drivit på utvecklingen av materialproducerade från förnyelsebara råvaror. CNF har fascinerande egenskapersom hög elasticitetsmodul och låga densiteter, vilket har gjort demattraktiva som strukturella material från hållbara källor som kan bilda 3Dnätverk.Kombinationen av katjoniska dendritiska polymerer och cellulosananofibriller utforskas i detta arbete och presenterar en spännandeutveckling av innovativa biomaterial som är antibakteriella ochbiokompatibla. En del av arbetet är fokuserad på syntesen av katjoniskadendritiska polymerer med varierande typer av katjoniska funktionalitetpå ytan genom att använda esterifieringsreaktioner som katalyseras avcesiumfluorid och därefter tiol-en-klickreaktioner. En annan del ärfokuserad på att skapa hybridhydrogeler som består av katjoniskadendritiska polymerer och anjoniska CNF. Vidare undersö, QC 2023-08-21Embargo godkänt av skolchef Amelie Eriksson Karlström via e-post 2023-08-22.

Through 270 million years of evolution, the finely tuned hierarchical structure of wood has been optimized for efficient nutrient transport and exceptional mechanical stability. Its distinctive orthotropic constitution can provide inspiration and design opportunities for the development of novel functional materials. In recent years, top-down modification approaches have adapted the wood structure for innovative applications, utilizing the hierarchical arrangement at different length scales. In doing so, preserving the structural integrity is of the essence. This thesis explores new top-down modification techniques for the functionalization and structural control of wood-based materials. With the intent of better preserving and utilizing the natural wood organization and native components, two different modification routes were explored on softwood Scots pine: complete lignin removal and in-situ lignin modification. Complete delignification was achieved through preventive crosslinking of the polysaccharide matrix, enhancing intercellular adhesion between tracheids and preventing the disintegration of the cellular arrangement after lignin removal. The second approach focused on chemical modification of lignin by sulfonation as an alternative to complete lignin removal, resulting in wood templates of high negative charge up to 375 µmol g-1 and with well-preserved residual lignin. Hot compression of the delignified wood veneers produced thin wood films with high optical transmittance of 71 % alongside exceptional tensile strength of 449 MPa and Young’s modulus of 50 GPa. Densification of lignin-retaining wood veneers yielded strong and transparent thin films with UV blocking ability. Additionally, these densified films could be easily recycled into discrete wood fibers. The integration of conductive polymers including poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) and polypyrrole in in-situ sulfonated wood resulted in bio-composites with high cond, Träets noggranna hierarkiska struktur har genom 270 miljoner års evolution optimerats för effektiv transport av näringsämnen och enastående mekanisk stabilitet. Dess distinkta ortotropa struktur kan inspirera samt ge utvecklingsmöjligheter för nya funktionella material. Via top-down metoder har man under de senaste åren lyckats nyttja träets hierarkiska struktur i olika storleksordningar för innovativa applikationer. I detta sammanhang är bevarandet av den strukturella integriteten av största vikt. Denna avhandling undersöker nya top-down metoder för att funktionalisera och kontrollera trämaterialens struktur. Med avsikt att bättre bevara och nyttja träets naturliga struktur och komponenter har två olika modifieringsmetoder undersökts för tall (pinus sylverstris): fullständig avlägsning av lignin samt in-situ modifiering av lignin. För att motverka cellstrukturens sönderfall efter fullständig delignifiering krävs det att polysackarider tvärbinds för att stärka vidhäftningen mellan trakeiderna. Modifiering av lignin (sulfonering) undersöktes som ett alternativ till fullständig delignifiering och resulterade i trämaterial med hög negativ laddning, upp till 375 µmol g-1, och med välbevarat lignin. Varmpressning av delignifierade träfanér resulterade i tunna träfilmer med hög optisk transmittans på 71 %, enastående draghållfasthet på 449 MPa och Youngs modul på 50 GPa. Förtätning av fanér med bevarat lignin gav starka och transparenta filmer med UV-blockerande förmåga vars massafibrer även kunde återvinnas. Integrering med elektriskt ledande polymerer, som poly(3,4-etylendioxytiopen) polystyrensulfonat (PEDOT:PSS) och polypyrrol, i in-situ-sulfonerat trä resulterade i biokompositer med hög konduktivitet, upp till 203 S m-1, och hög pseudo-kapacitans upp till 38 mF cm-2. Detta visar att kontroll av träkemin och redox-aktivitet hos lignin genom sulfonering är viktiga strategier för att tillverka kompositer med potential för hållbara energitillämpningar. Ett poröst trämat, QC 2023-08-21Embargo godkänt av skolchef Amelie Eriksson Karlström i e-post 2023-08-22.

The fundamental understanding concerning cellulose-cellulose interactions under wet and dry conditions remains unclear. This is especially true regarding the drying-induced association of cellulose, commonly described as an irreversible phenomenon called hornification. A fundamental understanding of the mechanisms behind hornification would contribute to new drying techniques for cellulose-based materials in the pulp and paper industry while at the same time enhancing material properties and facilitating the recyclability of cellulose-rich materials. In the present work, the irreversible joining of cellulose-rich surfaces has been studied by subjecting cellulose nanofibril (CNF) films to different heat treatments to establish a link between reswelling properties, structural characteristics as well as chemical and mechanical analyses. A heating time/temperature dependence was observed for the reswelling of the CNF films, which is related to the extent of hornification and is different for different chemical compositions of the fibrils. Further, the results indicate that hornification is related to a diffusion process and that the reswellability increases very slowly over long time, indicating that equilibrium is not reached. Hence, hornification is suggested to be a kinetically limited phenomenon governed by non-covalent reversible interactions and a time/temperature dependence on their forming and breaking., QC 20230829

Tree bark is normally a side-stream product but by an integrated bark biorefinery approach, valuable compounds may be recovered and used to replace fossil-based products. Norway spruce bark was extracted to obtain cellulose, which was chemically treated to produce cellulose oxalate (COX) which was homogenized to yield nanocellulose. The nanocellulose was used to produce Pickering emulsions with almond oil and hexadecane as organic phases. COX from dissolving pulp was used to study the effect of various raw materials on the emulsifying properties. The COX samples of bark and dissolving pulp contained a significant amount of hemicelluloses, which affected the viscosity results. The emulsion properties were affected by the organic phases and the aspect ratio. Emulsions using hexadecane were more stable than the emulsions using almond oil. Since the aspect ratio of bark was lower than that of the dissolving pulp, the emulsifying properties of the COX dissolving pulp was better. It has been shown that nanocellulose from cellulose oxalate of both spruce bark and dissolving pulp is a promising substitute for petroleum-based emulsifiers and surfactants. By utilizing bark, value-added products can be produced which may be economically beneficial for various industries in the future and their aim for climate-neutral products.

The development of wood-based thermoplastic polymersthat can replacesynthetic plastics is of high environmental importance, and previousstudies have indicated that cellulose-rich fiber containing dialcoholcellulose (ring-opened cellulose) is a very promising candidate material.In this study, molecular dynamics simulations, complemented with experiments,were used to investigate how and why the degree of ring opening influencesthe properties of dialcohol cellulose, and how temperature and presenceof water affect the material properties. Mechanical tensile properties,diffusion/mobility-related properties, densities, glass-transitiontemperatures, potential energies, hydrogen bonds, and free volumeswere simulated for amorphous cellulosic materials with 0-100%ring opening, at ambient and high (150 degrees C) temperatures, withand without water. The simulations showed that the impact of ringopenings, with respect to providing molecular mobility, was higherat high temperatures. This was also observed experimentally. Hence,the ring opening had the strongest beneficial effect on "processability"(reduced stiffness and strength) above the glass-transition temperatureand in wet conditions. It also had the effect of lowering the glass-transitiontemperature. The results here showed that molecular dynamics is avaluable tool in the development of wood-based materials with optimalthermoplastic properties., QC 20230630

In order to develop more economic uses of lignin, greater knowledge regarding its native structure is required. This can inform the development of optimized extraction methods that preserve desired structural properties. Current extraction methods alter the polymeric structure of lignin, leading to a loss of valuable structural groups or the formation of new non-native ones. In this study, Norway spruce (Picea abies) tissue-cultured cells that produce lignin extracellularly in a suspension medium were employed. This system enables the investigation of unaltered native lignin, as no physicochemical extraction steps are required. For the first time, this culture was used to investigate the interactions between lignin and xylan, a secondary cell wall hemicellulose, and to study the importance of lignin-carbohydrate complexes (LCCs) on the polymerization and final structure of extracellular lignin (ECL). This has enabled us to study the impact of xylan on monolignol composition and structure of the final lignin polymer. We find that the addition of xylan to the solid culture medium accelerates cell growth and impacts the ratio of monolignols in the lignin. However, the presence of xylan in the lignin polymerization environment does not significantly alter the structural properties of lignin as analyzed by two-dimensional nuclear magnetic resonance (NMR) spectroscopy and size exclusion chromatography (SEC). Nevertheless, our data indicate that xylan can act as a nucleation point, leading to more rapid lignin polymerization, an important insight into biopolymer interactions during cell wall synthesis in wood. Lignin structure and interactions with a secondary cell wall hemicellulose were investigated in a model cell culture: we found that the polymerization and final structure of lignin are altered when the hemicellulose is present during cell growth and monolignol production. The physicochemical interactions between lignin and xylan partly define the extractability and u, QC 20230630

Mass transport of liberated lignin fragments from pits and fiber walls into black liquor is considered a determining step in the delignification process. However, our current understanding of the diffusion of lignin through cellulose and the influential parameter on this process is very limited. A comprehensive and detailed study of lignin mass transport through cellulosic materials is, therefore, of great importance. In this study, diffusion cell methodology is implemented to systematically investigate the transport of fractionated kraft lignin molecules through model cellulose membranes. Pulping is a complex process and lignin is very heterogenous material therefore to perform a more detailed study on lignin diffusion, we included an additional solvent fractionation step. One of the benefits of this method is that the setup can be adjusted to various experimental conditions allowing the complex chemical reactions occurring during pulping, which would affect the mass transfer of lignin, to be avoided. Here, the effects of the alkalinity of the aqueous solution and molecular weight of the kraft lignin molecules on their diffusion were investigated. Additionally, NMR spectroscopy, size exclusion chromatography, and UV/Vis spectroscopy were used to characterize the starting material and the molecules that passed through the membrane. Lignin molecules detected in the acceptor chamber of the diffusion cells had lower molecular weights, indicating a size fractionation between the donor and acceptor chamber. UV/Vis showed higher concentrations of ionized conjugated kraft lignin molecules in the acceptor chamber, which is a sign of chemical fractionation. This study suggests that the diffusion of lignin through small cellulose pores can be enhanced by decreasing the average molecular weight of the diffusing kraft lignin molecules and increasing alkalinity., QC 20230705

Ultrasonication was used as a mean toincorporate glycerolor urea, yielding paper films with a ductility of up to 35%. Fiber-based materials are attractive sustainable alternativestofossil-based plastics, however, the lack of ductility (i.e., brittleness)limits their applicability in complex shapes as are often utilizedfor plastics. In this study, we hypothesize that it is possible toenhance the ductility of a cellulose-rich material by the incorporationof low molecular weight plasticizers (glycerol, urea, citric acid,and tannic acid). However, no significant effects could be observedafter swelling in the presence of plasticizers. To enhance any potentialeffect, it was decided to employ ultrasonication to mechanically disintegratethe fiber and aid the sorption of plasticizer prior to formation ofsheets from the treated fibers. Glycerol or urea in combination withultrasonication resulted in both internal and external fibrillationof the fibers, and it could be observed that the resulting fines createa film at the surface of the fibers in the formed sheets. Tensiletesting shows that this gives rise to a 100% increase in ductilitycompared to sheets from untreated fibers. The use of citric or tannicacid has the opposite effect, reducing ductility to a third of thatof the reference sheet. This is suggested to be due to the formationof covalent cross-links in the treated fibers, which also leads todifferent internal and external fibrillation mechanisms, as observedby scanning electron microscopy. The exceptionally high improvementof the strain-at-break for sheets from the glycerol- and urea-treatedfibers suggests that low molecular weight plasticizers affect theinternal properties of the fiber wall as well as the interactionsbetween the fine material forming in-between the fibers. The findingsfrom the current study suggest that the proposed approach to obtainductile cellulose-rich materials holds promise for the future, butit is also clear that more in-depth research is req, QC 20230630

Packaging plays a critical role in ensuring food safety and shelf life by protecting against e.g., moisture, gases, and light. Polyethylene (PE) is widely used in food packaging, but it is mainly produced from non-renewable resources and it is an inefficient oxygen and light barrier. In this study, the layer-by-layer (LbL) assembly of a sustainably produced lignin-based polymer (EH) with polyethylenimine (PEI) or chitosan (CH) was used to fabricate (partially or fully) bio-based coatings with the aim of improving barrier properties of PE films. The charge density of EH was calculated using a polyelectrolyte titration method and the hydrodynamic diameters of EH, PEI and CH were determined by Dynamic Light Scattering (DLS). LbL assembly was monitored in situ via Quartz Crystal Microbalance with Dissipation (QCM-D) and Stagnation Point Adsorption Reflectometry (SPAR). PE films were coated with a variable number of PEI/EH or CH/EH bilayers (BL) using an immersive LbL assembly method. Coated films were studied in terms of light-blocking ability, wettability, thermal behaviour, surface structure, as well as oxygen and water vapor barrier properties. QCM-D and SPAR data showed a stepwise multilayer formation and strong interactions between the oppositely charged polymers, with PEI/EH coating having a greater amount of deposited polymer compared to CH/EH coating at the same number of BL. Overall, light barrier properties and wettability of the coated films increased with the number of deposited bilayers. Coated PE films maintained the overall thermal behaviour of PE. A number of BL of 20 was found to be the most promising based on the studied properties. Selected samples showed improved oxygen and water vapor barrier properties, with PEI/EH coating performing better than CH/EH coating. Taken altogether, we demonstrated that a novel and sustainable lignin-based polymer can be combined with PEI or CH to fabricate (partially or fully) bio-based coatings for food packaging., QC 20230706

Adhesion is crucial for the development of mechanical properties in fibre-network materials, such as paper or other cellulose fibre biocomposites. The stress transfer within the network is possible through the fibre-fibre joints, which develop their strength during drying. Model surfaces are useful for studying the adhesive strength of joints by excluding other parameters influencing global performance, such as geometry, fibre fibrillation, or surface roughness. Here, a numerical model describes the development of adhesion between a cellulose bead and a rigid surface using an axisymmetric formulation, including moisture diffusion, hygroexpansion, and cohesive surfaces. It is useful for studying the development of stresses during drying. A calibration of model parameters against previously published contact and geometry measurements shows that the model can replicate the observed behaviour. A parameter study shows the influence of cohesive and material parameters on the contact area. The developed model opens possibilities for further studies on model surfaces, with quantification of the adhesion during pull-off measurements., QC 20230612

Studies have shown that the size of LNP depends on the molecular weight (M-w) of lignin. There is however need for deeper understanding on the role of molecular structure on LNP formation and its properties, in order to build a solid foundation on structure-property relationships. In this study, we show, for similar M-w lignins, that the size and morphology of LNPs depends on the molecular structure of the lignin macromolecule. More specifically, the molecular structure determined the molecular conformations, which in turn affects the inter-molecular assembly to yield size- and morphological-differences between LNPs. This was supported by density functional theory (DFT) modelling of representative structural motifs of three lignins sourced from Kraft and Organosolv processes. The obtained conformational differences are clearly explained by intra-molecular sandwich and/or T-shaped pi-pi stacking, the stacking type determined by the precise lignin structure. Moreover, the experimentally identified structures were detected in the superficial layer of LNPs in aqueous solution, confirming the theoretically predicted self-assembly patterns. The present work demonstrates that LNP properties can be molecularly tailored, consequently creating an avenue for tailored applications., QC 20230621

Improving the redispersion and recycling of dried cellulose nanofibrils (CNFs) without compromising their nanoscopic dimensions and inherent mechanical properties are essential for their large-scale applications. Herein, mixed-linkage (1,3;1,4)-beta-D-glucan (MLG) was studied as a rehydration medium for the redispersion and recycling of dried CNFs, benefiting from the intrinsic affinity of MLG to both cellulose and water molecules as inspired from plant cell wall. MLG from barley with a lower molar ratio of cellotriosyl to cellotetraosyl units was found homogeneously coated on CNFs, facilitating rehydration of the network of individualized CNFs. The addition of barley MLG did not impair the mechanical properties of the CNF/MLG composites as compared to neat CNFs nanopaper. With the addition of 10 wt% barley MLG, dry CNF/MLG composite film was successfully redispersed in water and recycled with well-maintained mechanical properties, while lichenan from Icelandic moss, cationic starch, and xyloglucan could not help the redispersion of dried CNFs., QC 20230607

Recently, chitosan has become attractive due to being biodegradable, biocompatible and renewable. However, the weak mechanical properties of chitosan films limit their large-scale application. In this work, a strategy of blending TEMPO, oxidized CNF (TOCN) and chitosan was developed to fabricate nanocomposite films in order to improve the mechanical properties and maintain biocompatibility. The TOCN/chitosan nanocomposite films exhibited excellent optical transmittance (>85%) and extremely high tensile strength of 235 MPa. The good compatibility of TOCN and chitosan chains, good dispersion of chitosan aggregates and the presence of stiff TOCN crystal domains are the main reasons for getting improved mechanical strength of composite films. The films showed good biocompatible properties based on the cell activity assay results. Furthermore, they were stable in PBS buffer for more than 6 months without significant degradation. The TOCN/chitosan nanocomposite films with these excellent properties could be employed in medical applications., QC 20230612

In light of the need to redesign industrially produced materials by utilizing renewable resources, nanoscopic forms of cellulose are regarded as a valuable asset. In this work, the potential of cellulose nanofibrils (CNFs) as an unconventional nanoadditive for a polyester-melamine coil coating formulation is explored. CNFs, hydrophilic nanomaterials with high aspect ratios, were successfully incorporated in the solvent-borne formulation. Coatings were prepared with extremely low loadings of the nanoadditive (0.5 and 0.7 wt%). At these concentrations, the volume fraction of the nanofibrils in the coatings was calculated to be close to their percolation threshold. Two different pathways of CNF surface modification were applied to allow for a good compatibilization in the resin matrix, and the formulations were cured in two different settings. The effective compatibilization of the nano -additive led to a significant variation of the viscoelastic properties in the coatings containing CNFs. The results from dynamic mechanical analysis (DMA) highlighted the effect of CNFs on the crosslinked network at the nanoscale, resulting in an increase in Tg. Additionally, an increase in the stress at break and Young's modulus was determined by tensile testing, while satisfactory elongation at break was preserved. Other relevant effects induced by the presence of CNFs on the properties of the coatings were highlighted, such as a significant matt effect, increased surface roughness and lower scratch resistance. A preliminary evaluation of the water barrier properties by electrochemical impedance spectroscopy (EIS) is also presented, suggesting that the incorporation of a hydrophilic nanoadditive did not lead to a deterioration of the coatings' performance., QC 20230607

Although organosolv processes using high-boiling solvents have been investigated in recent decades for developing novel industrial processes, there are potential benefits of using high-boiling point solvents for traditional sulphate-based cooking processes, both from an industrial perspective and from a laboratory perspective. Using high-boiling solvents, experiments can be done under atmospheric conditions, thus making it easier to continually monitor laboratory experiments and extracting aliquots at desired intervals. Using such a system, alkaline consumption was monitored during impregnation of spruce chips in glycerol media using chemical charges of 1 M NaOH and 0.1 M NaHS, i. e., kraft pulping conditions, and compared to a similar investigation of alkaline consumption in water media using steel autoclaves. The resulting data was fitted to a first order kinetic model, with an apparent activation energy of 22 kJ mol-1 in glycerol media. Finally, a "normal quality pulp"of kappa number 28 and a viscosity of 1113 ml g-1 was successful produced using a cooking process with an impregnation step at 140 °C for 3 h and a cooking step at 160 °C for 4 h. A nuclear magnetic resonance study on the dissolved lignin produced for said experiment showed characteristics typical of other kraft lignins., QC 20230615