<p>The adsorption of cationic polyacrylamide (C-PAM) and silicananoparticles onto a model surface of silicon oxide wascompared with the adsorption of C-PAM to fibres and theirinfluence on flocculation of a fibre suspension. An increase inionic strength affects the polyelectrolyte adsorption indifferent ways for these two systems. With the silica surface,an increase in the ionic strength leads to a continuousincrease in the adsorption. However, on a cellulose fibre, theadsorption increases at low ionic strength (1 to 10 mM NaCl)and then decreases at higher ionic strength (10 to 100 mMNaCl). It was shown that the adsorption of nanoparticles ontopolyelectrolyte-covered surfaces has a great effect on both theadsorbed amount and the thickness of the adsorbed layer. Theresults showed that electrostatic interactions were thedominating force for the interaction between both the fibresand the polyelectrolytes, and between the polyelectrolytes andthe silica particles. Furthermore, at higher NaClconcentrations, a significant non-ionic interaction between thesilicon oxide surface/particles and the C-PAM was observed.</p><p>The adsorption rate of C-PAM onto fibres was rapid andquantitative adsorption was detected in the time range between1 and 8 s at polyelectrolyte addition levels below 0.4 mg/g.Conversely, an increase in the amount of added polymer leads toan increased polymer adsorption up to a quasi-static saturationlevel. However, after a few seconds this quasi-staticsaturation level was significantly lower than the level reachedat electrostatic“equilibrium”. The adsorbed amountof charges at full surface coverage after 1 to 8 s contact timecorresponded to only 2 % of the total fibre charge, whereasafter 30 minutes it corresponded to 15 % of the total fibrecharge. This shows that a full surface coverage at shortcontact times is not controlled by surface charge. Based onthese results, it is suggested that a combination of anon-equilibrium charge barrier against adsorption and ageometric restriction can explain the difference between theadsorption during 1 to 8 s and the adsorption after 30 minutes.With increasing time, the cationic groups are neutralised bythe charges on the fibre as the polyelectrolyte reconforms to aflat conformation on the surface.</p><p>The addition of a high concentration of C-PAM to a fibresuspension resulted in dispersion rather than flocculation.This behaviour is most likely due to an electrostericstabilisation of the fibres when the polyelectrolyte isadsorbed. Flocculation of the fibre suspension occurred at lowadditions of C-PAM. A maximum in flocculation was found ataround 50 % surface coverage and dispersion occurred above 100% surface coverage. It was also shown that for a given level ofadsorbed polymer, a difference in adsorption time between 1 and2 seconds influenced the flocculation behaviour. An optimum inflocculation at 50 % surface coverage in combination with theimportance of polymer reconformation time at these shortcontact times showed that the C-PAM induced fibre flocculationagrees with La Mer and Healy’s description of bridgingflocculation.</p><p>A greater degree of flocculation was observed with theaddition of silica nanoparticles to the fibre suspension thanin the single polyelectrolyte system. Flocculation increased asa function of the concentration of added nanoparticles until0.5 mg/g. At higher additions the flocculation decreased againand this behaviour is in agreement with an extended model formicroparticle-induced flocculation. An increase in flocculationwas especially pronounced for the more extended silica-2particles. This effect is attributed to the more extendedpolyelectrolyte layer, since the adsorbed amount wasessentially the same for both silica particles.</p><p>Finally it was found that fines from the wood fibres had asignificant effect on the flocculation. When fines were added,a greater degree of flocculation was detected. Furthermore, itwas also more difficult to redisperse the fibres with polymerin the presence of fines.</p><p><b>Keywords:</b>Adsorption, bridging, cationic polymers,cellulose fibres, electrosteric stabilisation flocculation,ionic strength, nanoparticle, polyelectrolyte, reconformation,retention aids and silica</p>

Cationized tannins as a retention aid for cellulose fibre Daniel Bäckström   Abstract The purpose of this study was to try cationized tannins as a potential retention aid for cellulose fibres in papermaking and to compare their potential with starch which already is commonly used. The study also tried to find other advantages with using tannins as a retention aid. Synthetic retention aids like polyacrylamide is also commonly used in papermaking, with good results. Synthetic retention aids are long-lived and their long-term effect on the environment is unkown. Therefore the demands are growing for more bio-degradable products. Measure glass, turbidity removal and COD was used in this study to analyse tannins as a retention aid on cellulose fibres. The results showed very clear water and a higher flocculation compared to the glass without tannins. 500 ppm tannins added to recycled fibres showed the best results for both flocculation and clear water as well as the highest turbidity removal, from 85 to 24 FTU. Different tannins was used in this study, and Tanfloc from the bark of the Acacia tree showed the best results. In the comparison between cationized starch and Tanfloc, Tanfloc showed better results for both flocculation and clearer water. Tannins shows potential as a retention aid for cellulose fibres, but clearer water and higher flocculation is not enough to determine tannins as a retention aid. They also show potential to solve the problem with bacteria in paper making because of their antibacterial effect. However, more tests and other methods needs to be done to show tannins potential as a retention aid.

The adsorption of cationic polyacrylamide (C-PAM) and silicananoparticles onto a model surface of silicon oxide wascompared with the adsorption of C-PAM to fibres and theirinfluence on flocculation of a fibre suspension. An increase inionic strength affects the polyelectrolyte adsorption indifferent ways for these two systems. With the silica surface,an increase in the ionic strength leads to a continuousincrease in the adsorption. However, on a cellulose fibre, theadsorption increases at low ionic strength (1 to 10 mM NaCl)and then decreases at higher ionic strength (10 to 100 mMNaCl). It was shown that the adsorption of nanoparticles ontopolyelectrolyte-covered surfaces has a great effect on both theadsorbed amount and the thickness of the adsorbed layer. Theresults showed that electrostatic interactions were thedominating force for the interaction between both the fibresand the polyelectrolytes, and between the polyelectrolytes andthe silica particles. Furthermore, at higher NaClconcentrations, a significant non-ionic interaction between thesilicon oxide surface/particles and the C-PAM was observed. The adsorption rate of C-PAM onto fibres was rapid andquantitative adsorption was detected in the time range between1 and 8 s at polyelectrolyte addition levels below 0.4 mg/g.Conversely, an increase in the amount of added polymer leads toan increased polymer adsorption up to a quasi-static saturationlevel. However, after a few seconds this quasi-staticsaturation level was significantly lower than the level reachedat electrostatic“equilibrium”. The adsorbed amountof charges at full surface coverage after 1 to 8 s contact timecorresponded to only 2 % of the total fibre charge, whereasafter 30 minutes it corresponded to 15 % of the total fibrecharge. This shows that a full surface coverage at shortcontact times is not controlled by surface charge. Based onthese results, it is suggested that a combination of anon-equilibrium charge barrier against adsorption and ageometric restriction can explain the difference between theadsorption during 1 to 8 s and the adsorption after 30 minutes.With increasing time, the cationic groups are neutralised bythe charges on the fibre as the polyelectrolyte reconforms to aflat conformation on the surface. The addition of a high concentration of C-PAM to a fibresuspension resulted in dispersion rather than flocculation.This behaviour is most likely due to an electrostericstabilisation of the fibres when the polyelectrolyte isadsorbed. Flocculation of the fibre suspension occurred at lowadditions of C-PAM. A maximum in flocculation was found ataround 50 % surface coverage and dispersion occurred above 100% surface coverage. It was also shown that for a given level ofadsorbed polymer, a difference in adsorption time between 1 and2 seconds influenced the flocculation behaviour. An optimum inflocculation at 50 % surface coverage in combination with theimportance of polymer reconformation time at these shortcontact times showed that the C-PAM induced fibre flocculationagrees with La Mer and Healy’s description of bridgingflocculation. A greater degree of flocculation was observed with theaddition of silica nanoparticles to the fibre suspension thanin the single polyelectrolyte system. Flocculation increased asa function of the concentration of added nanoparticles until0.5 mg/g. At higher additions the flocculation decreased againand this behaviour is in agreement with an extended model formicroparticle-induced flocculation. An increase in flocculationwas especially pronounced for the more extended silica-2particles. This effect is attributed to the more extendedpolyelectrolyte layer, since the adsorbed amount wasessentially the same for both silica particles. Finally it was found that fines from the wood fibres had asignificant effect on the flocculation. When fines were added,a greater degree of flocculation was detected. Furthermore, itwas also more difficult to redisperse the fibres with polymerin the presence of fines. <b>Keywords:</b>Adsorption, bridging, cationic polymers,cellulose fibres, electrosteric stabilisation flocculation,ionic strength, nanoparticle, polyelectrolyte, reconformation,retention aids and silica / NR 20140805

Modificações químicas foram aplicadas às fibras celulósicas e ao amido com o objetivo de obter produtos com uma camada termoplástica externa, preservando a parte interna desses substratos (não modificada). O produto final deveria se comportar como um material compósito onde a parte interna não modificada é o agente de reforço e a camada termoplástica a matriz. As modificações foram realizadas através da inserção de pequenas cadeias de óxido propileno a cadeia carbônica do polissacarídeo (celulose e amido). As cadeias de poli(oxido propileno) enxertadas proporcionará uma camada termoplástica em torno da porção de polissacarídeo não modificada. A obtenção destes materiais pode dispensar as etapas de mistura e permitir o processamento térmico sem a necessidade de utilização de um segundo componente (matriz), uma vez que a própria capa polimérica desempenharia este papel. A construção da capa polimérica envolvente foi conduzida através da reação da celulose ou amido pré-ativados com o óxido de propileno. A etapa de ativação foi realizada com o tratamento dos substratos com KOH ou DABCO e a reação de enxertia foi realizada em sistema heterogêneo. Os materiais obtidos utilizando esses tratamentos foram caracterizados por diferentes técnicas (FTIR, Raios-X, MEV, TG, DSC, Ângulo de contato e ensaios de Resistência à Tração). Os resultados obtidos demonstraram que é possível de produzir materiais com características termoplásticas reforçadas através da reação em uma única etapa, sem a necessidade de laboriosos procedimentos sintéticos. / Chemical modifications were applied to cellulosic materials and starch with the objective to obtain products with an external thermoplastic layer while preserving the inner part of these substrates. The final products should behave as composite materials where the unmodified inner part is the reinforcement agent and the thermoplastic layer the matrix. The modifications were performed by grafting polypropylene oxide short chains to the polysaccharide backbone (cellulose and starch). The grafted polypropylene oxide chains will render a thermoplastic layer around the unmodified polysaccharide portions. The attainment of these materials can excuse the stages of mixture and allow the thermal processing without the necessity of use the second component (matriz), a time that the proper polymeric layer would play this role. The construction of the involving polymeric layer was conducted by reacting pre-activated cellulose (or starch) and propylene oxide (PO). The activation step was performed with KOH (or DABCO) treatment and the grafting reaction was carried through in heterogeneous system. The materials obtained following these treatments were characterized by different techniques (FTIR, X-Ray, MEV, TG, DSC, Contact Angle and Mechanical Analyses). The results had demonstrated that it is possible to produce materials with strengthened thermoplastic characteristics through the reaction in an only stage, without the necessity of laborious synthetic procedures.

Analysis of calcium and oxygen atom arrays of known cement minerals and the structures of cellulose polymorphs were performed to see if it was possible to arrange a cellulose fibre on a cement mineral face such that the fibre is bonded by a repeating array of hydrogen or hydroxide coordination bonds for the full length of the attachment. Of the sixteen important cement minerals modelled, xonotlite, foshagite, tricalcium aluminate hydrate, chondronite and rosenhahnite could form such bonds to modified cellulose fibre. However, this was not the case for other cement minerals, especially tobermorite. Alumium hydroxide, when added to cement-quartz pastes and autoclaved at 180 degrees C, was found to improve the cement's ability to resist carbonation. / Doctor of Philosophy (PhD)

Das maximale Trubaufnahmevermögen eines Filterkuchens ist ein wichtiges Kriterium für die Vorhersagbarkeit der Standzeit des Filters. In Praxisfiltrationen in Brauereien konnte nachgewiesen werden, dass sich die Filtration mit Zellulose als Filterhilfsmittel grundsätzlich in zwei Bereiche unterteilen lässt. Zunächst verläuft der Anstieg der Druckdifferenz linear, geht dann aber zu jeweils versuchsspezifisch unterschiedlichen Zeitpunkten in den exponentiellen Verlauf über, was auf eine Kompaktierung der freien Durchgangskanäle des Filterkuchens zurückzuführen ist. Mehrmalige Regenerationen verbessern die Trübungsreduzierung der Filterhilfsmittelmischung, was durch verminderte Wasserwerte und Darcy-Werte im Labor nachgewiesen werden konnte. Wie bereits aus der Kieselgurfiltration bekannt, sind Standzeit und Trübungsreduzierung der Zellulosefiltration in entscheidendem Maß von der Filtrierbarkeit der Biere abhängig und mit den Werten eines Kieselgurfilters vergleichbar.

Thesis (PhD) -- University of Western Sydney, 2001. / "A thesis submitted for the degree of Doctor of Philosophy in the University of Western Sydney." Bibliography: leaves 163 - 170.

Modificações químicas foram aplicadas às fibras celulósicas e ao amido com o objetivo de obter produtos com uma camada termoplástica externa, preservando a parte interna desses substratos (não modificada). O produto final deveria se comportar como um material compósito onde a parte interna não modificada é o agente de reforço e a camada termoplástica a matriz. As modificações foram realizadas através da inserção de pequenas cadeias de óxido propileno a cadeia carbônica do polissacarídeo (celulose e amido). As cadeias de poli(oxido propileno) enxertadas proporcionará uma camada termoplástica em torno da porção de polissacarídeo não modificada. A obtenção destes materiais pode dispensar as etapas de mistura e permitir o processamento térmico sem a necessidade de utilização de um segundo componente (matriz), uma vez que a própria capa polimérica desempenharia este papel. A construção da capa polimérica envolvente foi conduzida através da reação da celulose ou amido pré-ativados com o óxido de propileno. A etapa de ativação foi realizada com o tratamento dos substratos com KOH ou DABCO e a reação de enxertia foi realizada em sistema heterogêneo. Os materiais obtidos utilizando esses tratamentos foram caracterizados por diferentes técnicas (FTIR, Raios-X, MEV, TG, DSC, Ângulo de contato e ensaios de Resistência à Tração). Os resultados obtidos demonstraram que é possível de produzir materiais com características termoplásticas reforçadas através da reação em uma única etapa, sem a necessidade de laboriosos procedimentos sintéticos. / Chemical modifications were applied to cellulosic materials and starch with the objective to obtain products with an external thermoplastic layer while preserving the inner part of these substrates. The final products should behave as composite materials where the unmodified inner part is the reinforcement agent and the thermoplastic layer the matrix. The modifications were performed by grafting polypropylene oxide short chains to the polysaccharide backbone (cellulose and starch). The grafted polypropylene oxide chains will render a thermoplastic layer around the unmodified polysaccharide portions. The attainment of these materials can excuse the stages of mixture and allow the thermal processing without the necessity of use the second component (matriz), a time that the proper polymeric layer would play this role. The construction of the involving polymeric layer was conducted by reacting pre-activated cellulose (or starch) and propylene oxide (PO). The activation step was performed with KOH (or DABCO) treatment and the grafting reaction was carried through in heterogeneous system. The materials obtained following these treatments were characterized by different techniques (FTIR, X-Ray, MEV, TG, DSC, Contact Angle and Mechanical Analyses). The results had demonstrated that it is possible to produce materials with strengthened thermoplastic characteristics through the reaction in an only stage, without the necessity of laborious synthetic procedures.

Naturskyddsföreningen gav författarna uppgiften att undersöka förekommande viskosprocesser och alternativa regenereringsprocesser, detta för att identifiera hur hållbara de är ur ett miljöperspektiv och vilka processer som går att applicera på bambu. Detta för att se möjligheten att märka bambuviskos med Bra Miljöval och för att klargöra frekvent uppkommande frågor angående bambuviskos. Syftet är att se på de olika processernas kemiska innehåll samt vilka utsläpp de orsakar till luft och vatten. Ett delmål med rapporten är att den ska kunna användas som material vid vidareutveckling av kriterierna för Bra Miljöval Textil. Resultat som erhållits vid jämförelser av studerad litteratur är att de betydande faktorerna för miljöpåverkan från massaframställningen samt viskos- och lyocellprocessen beror av: använda kemikalier i processen, energianvändningen och vilken typ av energi, möjligheten till rening av utsläpp till luft och vatten samt återvinning av energi och kemikalier. Beroende på vilket råmaterial som används vid massaframställningen kan skillnader i markanvändning, användning av bekämpningsmedel och gödningsmedel samt upptagande av koldioxid skilja sig. Massa- och fiberframställning bör vara integrerade då energiförbrukning och mängd kemikalier kan minskas. Energin kan dessutom återvinnas till större utsträckning.Genom miljömärkningar från oberoende organisationer blir det lättare för konsumenter att göra miljömedvetna val och veta vad märkningarna står för. Sammanfattningsvis ska det påpekas att om regenererad bambu framställs som den görs idag är den ingen hållbar fiber, men sker framställningen i en integrerad process där kemikalier och energi återvinns samt rening av utsläpp till luft och vatten sker, kan bambuviskos bli en hållbar fiber för framtiden. The Swedish Society for Nature Conservation (SSNC) gave the authors the task to investigative present viscose processes and alternative regeneration processes to identify how sustainable they are from an environmental perspective, and examine which processes that can be applied to bamboo. This to see the possibility to label bamboo viscose with “Bra Miljöval” (Good Environmental Choice), which is the eco-label of SSNC, and to clarify the frequently emerging issues concerning bamboo viscose. The aim is to look at the various processes, their chemical content and the emissions they cause to air and water. Another objective of the report is that it can be used as material for further development of the criteria for “Bra Miljöval”.Results obtained when comparing the studied literature is that the significant factors of the environmental impact from the pulp production, the viscose and lyocell processes depends on: chemicals used in the process, energy and energy source, the possibility of purifying emissions to air and water and recycling of energy and chemicals. Depending on the raw materials used for pulp production, differences in land use, use of pesticides and fertilizers as well as absorption of carbon dioxide differ. Pulp and fibre production should be integrated to reduce energy consumption and the amount of chemicals used. The energy can also be recycled to a greater extent.Eco-labels from independent organizations will make it easier for consumers to make environmentally conscious choices and be aware of what the labels stand for.In conclusion, it should be noted that if the regenerated bamboo is produced as it is today, it is not a sustainable fibre. If the production is done through an integrated process in which chemicals and energy recovery and purification of air and water occurs, bamboo viscose can be a sustainable fibre for the future. / Program: Textilingenjörsutbildningen

Das maximale Trubaufnahmevermögen eines Filterkuchens ist ein wichtiges Kriterium für die Vorhersagbarkeit der Standzeit des Filters. In Praxisfiltrationen in Brauereien konnte nachgewiesen werden, dass sich die Filtration mit Zellulose als Filterhilfsmittel grundsätzlich in zwei Bereiche unterteilen lässt. Zunächst verläuft der Anstieg der Druckdifferenz linear, geht dann aber zu jeweils versuchsspezifisch unterschiedlichen Zeitpunkten in den exponentiellen Verlauf über, was auf eine Kompaktierung der freien Durchgangskanäle des Filterkuchens zurückzuführen ist. Mehrmalige Regenerationen verbessern die Trübungsreduzierung der Filterhilfsmittelmischung, was durch verminderte Wasserwerte und Darcy-Werte im Labor nachgewiesen werden konnte. Wie bereits aus der Kieselgurfiltration bekannt, sind Standzeit und Trübungsreduzierung der Zellulosefiltration in entscheidendem Maß von der Filtrierbarkeit der Biere abhängig und mit den Werten eines Kieselgurfilters vergleichbar.