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Artykuły w czasopismach na temat "Cellulose fibre"
Ouajai, Sirisart, Peerachai Ruangwilairat, Kitti Ongwongsakul, Thanawadee Leejarkpai i Robert A. Shanks. "Morphology and Structure of Modified Oil Palm Empty Fruit Bunch Cellulose Fibre". Advanced Materials Research 93-94 (styczeń 2010): 607–10. http://dx.doi.org/10.4028/www.scientific.net/amr.93-94.607.
Pełny tekst źródłaCordin, Michael, i Thomas Bechtold. "Physical properties of lyocell-reinforced polypropylene composites from intermingled fibre with varying fibre volume fractions". Journal of Thermoplastic Composite Materials 31, nr 8 (19.10.2017): 1029–41. http://dx.doi.org/10.1177/0892705717734594.
Pełny tekst źródłaSobczak, L., A. Limper, H. Keuter, K. Fischer i A. Haider. "Polypropylene-cellulose Innovative Compounding Technology". Polymers from Renewable Resources 3, nr 1 (luty 2012): 27–32. http://dx.doi.org/10.1177/204124791200300103.
Pełny tekst źródłaSumithra, Murugesan, i Gayathri Murugan. "Extraction and characterization of natural fibres form Elettaria Cardamomum". Tekstilna industrija 69, nr 2 (2021): 30–33. http://dx.doi.org/10.5937/tekstind2102030s.
Pełny tekst źródłaStevulova, Nadezda, Viola Hospodarova, Vojtech Vaclavik, Tomas Dvorsky i Tomas Danek. "Characterization of cement composites based on recycled cellulosic waste paper fibres". Open Engineering 8, nr 1 (10.11.2018): 363–67. http://dx.doi.org/10.1515/eng-2018-0046.
Pełny tekst źródłaAbdullah, ABM, Maruf Abony, MT Islam, MS Hasan, MAK Oyon i Md Bokhtiar Rahman. "Extraction and Proximate Study of Sansevieria Trifasciata L. As Fibre Source for Textile and Other Uses". Journal of the Asiatic Society of Bangladesh, Science 46, nr 2 (29.06.2021): 155–62. http://dx.doi.org/10.3329/jasbs.v46i2.54411.
Pełny tekst źródłaArdanuy, Mònica, Marcelo Antunes i Jose Ignacio Velasco. "Preparation and Characterization of Cellulosic Fibre-Reinforced Polypropylene Foams". Advanced Materials Research 123-125 (sierpień 2010): 1183–86. http://dx.doi.org/10.4028/www.scientific.net/amr.123-125.1183.
Pełny tekst źródłaSchmidt, Vivian Consuelo Reolon, i João Borges Laurindo. "Characterization of foams obtained from cassava starch, cellulose fibres and dolomitic limestone by a thermopressing process". Brazilian Archives of Biology and Technology 53, nr 1 (luty 2010): 185–92. http://dx.doi.org/10.1590/s1516-89132010000100023.
Pełny tekst źródłaRuan, Yong-Ling. "Rapid cell expansion and cellulose synthesis regulated by plasmodesmata and sugar: insights from the single-celled cotton fibre". Functional Plant Biology 34, nr 1 (2007): 1. http://dx.doi.org/10.1071/fp06234.
Pełny tekst źródłaAuernhammer, Julia, Tom Keil, Binbin Lin, Jan-Lukas Schäfer, Bai-Xiang Xu, Markus Biesalski i Robert W. Stark. "Mapping humidity-dependent mechanical properties of a single cellulose fibre". Cellulose 28, nr 13 (14.07.2021): 8313–32. http://dx.doi.org/10.1007/s10570-021-04058-4.
Pełny tekst źródłaRozprawy doktorskie na temat "Cellulose fibre"
Larsson, Per A. "Dimensional Stability of Paper : Influence of Fibre-Fibre Joints and Fibre Wall Oxidation". Licentiate thesis, KTH, Fiberteknologi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4635.
Pełny tekst źródłaPaper is a very versatile material. Nevertheless, there are several factors limiting its usefulness, and one of the major issues is that cellulosic and ligno-cellulosic fibres lower their free energy by sorbing water and this water changes the dimensions of the paper. This phenomenon is usually referred to as a lack of dimensional stability and is often evident as misregister during multicolour printing or curl, cockle and wavy edges during printing, copying and storage or, with a wider definition, also as a shortened life-time of boxes during storage due to mechano-sorptive creep. The work described in this thesis aims to study and quantify the importance of the different mechanisms causing water-induced dimensional changes in a fibre network and to investigate how to improve the dimensional stability of ligno-cellulosic materials. This has been done both by altering the fiber properties such as the moisture sorptivity and by changing the adhesion and degree of contact within the fibre-fibre joints. The properties of the fibre-fibre joints have been varied by drying laboratory sheets both under restraint and freely to minimise the generation of built-in stresses. Bleached kraft fibres were treated using the polyelectrolyte multilayer (PEM) technique to improve the adhesion between the fibres and to increase the molecular contact within the joints. In contrast, the degree of contact was impaired by hornifying the fibres before sheet preparation. For sheets allowed to dry freely, the PEM-treatment increased the hygroexpansion coefficient, i.e. the dimensional movement normalised with respect to the change in moisture content, when subjected to changes in relative humidity whereas the hornification process resulted in a slightly lowered hygroexpansion coefficient. However, when the sheets were dried under restraint, the different joint and fibre modifications led to no difference in hygroexpansion coefficient. This was interpreted as being a result of an increase in the total contact zone between the fibres when the sheets were dried under restraint, with a greater extension in the outof- plain direction of the joint resulting in a transfer of a larger part of the transverse swelling to the in-plane expansion. The sorptivity of the fibres was changed by oxidising the C2-C3 bond of the 1,4- glucans with periodate. This most likely created covalent cross-links in the fibre wall both improved the integrity of the fibre wall by locking adjacent fibril lamellae to each other and also removed possible sites for water sorption onto the cellulose surfaces. Periodate oxidation also led to a decrease in the crystallinity of the cellulose within the fibres, making more cellulose hydroxyl groups available for the adsorption of water molecules. This means that the oxidation both decreased and increased the interaction between the fibre wall and moisture but, on two different structural levels. The crosslinks significantly reduced the sorption rate when the papers was subjected to changes in relative humidity, as long as the fibres were not subjected to humidities close to saturation. The smaller change in moisture content when the relative humidity was changed between 20 and 85 % RH meant that the dimensional stability of the crosslinked sheets was increased. On the other hand, the hygroexpansion coefficient was increased in the case of papers made from fibres with the highest degree of oxidation, i.e. the sheets became more sensitive to absolute changes in moisture content.
QC 20101117
Larsson, Per. "Dimensional Stability of Paper Influence of Fibre-Fibre Joints and Fibre Wall Oxidation". Licentiate thesis, KTH, Fibre and Polymer Technology, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4635.
Pełny tekst źródłaPapper är ett mycket mångsidigt material. Trots detta finns det ett flertal egenskaper som begränsar papperets användbarhet. Ett av de större problemen med cellulosa- och lignocellulosafibrer är att de sänker sin fria energi genom att sorbera vatten, och denna sorption förändrar papperets dimensioner. Detta fenomen kallas vanligtvis för bristfällig dimensionsstabilitet och uppträder i form av registerfel vid flerfärgstryck eller som krullning, buckling och vågiga papperskanter vid utskrift, kopiering och lagring, eller med en vidare definition som förkortad livslängd hos lådor på grund av mekanosorptivt kryp.
Avsikten med denna avhandling har varit att studera och kvantifiera vilka egenskaper som styr, och hur de påverkar, den vatteninducerade dimensionsförändringen som sker hos ett fibernätverk, samt hur dess dimensionsstabilitet kan förbättras. Detta har studerats både genom att ändra fiberns fuktsorptionsegenskaper och genom att förändra adhesionen och kontaktgraden mellan fibrerna i fiber-fiberfogarna. Fogegenskaperna har också varierats genom att tillverka laboratorieark torkade under inspänning samt ark torkade fritt för att minimera mängden inbyggda spänningar i arket.
Blekt kraftmassa har behandlats med polyelektrolytmultilager (PEM) för att förbättra adhesionen mellan fibrerna och för att öka kontaktgraden mellan fibrerna i fogen. Kontaktgraden har även minskats genom förhorning av fibrerna före arkformning. För de ark som fick torka fritt gav PEM-behandlingen en ökad hygroexpansionskoefficient, det vill säga dimensionsförändringen normaliserad mot förändringen i fuktinnehåll, vid samma förändring i relativ luftfuktighet medan förhorningen minskade hygroexpansionskoefficienten något. Om arken emellertid torkades under inspänning observerades ingen skillnad i hygroexpansionskoefficient mellan de olika fibermodifieringarna. Detta tolkades som ett resultat av en ökad kontaktzon och en större utbredning ut ur fogens plan, när arken torkades utan inspänning. En utbredning som medför att en större del av fiberns transversella expansion överförs som expansion i pappersplanet.
Fibrernas fuktsorptionsegenskaper förändrades genom natriumperjodatoxidering av 1,4-glukanernas C2-C3-bindning. Detta skapade sannolikt tvärbindningar i fiberväggen som förbättrade fiberväggens tålighet både genom att låsa fibrillerna närmare varandra och genom att ta bort potentiella adsorptionssäten som annars är tillgängliga för vattenadsorption. Perjodatoxidationen minskar också fibrernas kristallinitet och således frigjorde oxidationen hydroxylgrupper där vattenmolekyler kan adsorbera. Detta innebar att oxidationen både minskade och ökade interaktionen mellan vatten och fibervägg, men dock på olika strukturell nivå. Tvärbindningarna visade sig också märkbart reducera sorptionshastigheten när arken utsattes för en förändrad luftfuktighet så länge de inte tidigare utsatts för relativa luftfuktigheter nära mättnad. Som ett resultat av den lägre förändringen i fuktinnehåll vid en förändring i luftfuktighet från 20 till 85 % RF minskade dimensionsförändringens amplitud för de tvärbundna arken upp till 30 %. Emellertid uppvisade de tvärbundna arken en högre hygroexpansionskoefficeint, vilket innebär att de blev mer känsliga för absoluta förändringar i fuktinnehåll.
Paper is a very versatile material. Nevertheless, there are several factors limiting its usefulness, and one of the major issues is that cellulosic and ligno-cellulosic fibres lower their free energy by sorbing water and this water changes the dimensions of the paper. This phenomenon is usually referred to as a lack of dimensional stability and is often evident as misregister during multicolour printing or curl, cockle and wavy edges during printing, copying and storage or, with a wider definition, also as a shortened life-time of boxes during storage due to mechano-sorptive creep.
The work described in this thesis aims to study and quantify the importance of the different mechanisms causing water-induced dimensional changes in a fibre network and to investigate how to improve the dimensional stability of ligno-cellulosic materials. This has been done both by altering the fiber properties such as the moisture sorptivity and by changing the adhesion and degree of contact within the fibre-fibre joints. The properties of the fibre-fibre joints have been varied by drying laboratory sheets both under restraint and freely to minimise the generation of built-in stresses.
Bleached kraft fibres were treated using the polyelectrolyte multilayer (PEM) technique to improve the adhesion between the fibres and to increase the molecular contact within the joints. In contrast, the degree of contact was impaired by hornifying the fibres before sheet preparation. For sheets allowed to dry freely, the PEM-treatment increased the hygroexpansion coefficient, i.e. the dimensional movement normalised with respect to the change in moisture content, when subjected to changes in relative humidity whereas the hornification process resulted in a slightly lowered hygroexpansion coefficient. However, when the sheets were dried under restraint, the different joint and fibre modifications led to no difference in hygroexpansion coefficient. This was interpreted as being a result of an increase in the total contact zone between the fibres when the sheets were dried under restraint, with a greater extension in the outof- plain direction of the joint resulting in a transfer of a larger part of the transverse swelling to the in-plane expansion.
The sorptivity of the fibres was changed by oxidising the C2-C3 bond of the 1,4- glucans with periodate. This most likely created covalent cross-links in the fibre wall both improved the integrity of the fibre wall by locking adjacent fibril lamellae to each other and also removed possible sites for water sorption onto the cellulose surfaces. Periodate oxidation also led to a decrease in the crystallinity of the cellulose within the fibres, making more cellulose hydroxyl groups available for the adsorption of water molecules. This means that the oxidation both decreased and increased the interaction between the fibre wall and moisture but, on two different structural levels. The crosslinks significantly reduced the sorption rate when the papers was subjected to changes in relative humidity, as long as the fibres were not subjected to humidities close to saturation. The smaller change in moisture content when the relative humidity was changed between 20 and 85 % RH meant that the dimensional stability of the crosslinked sheets was increased. On the other hand, the hygroexpansion coefficient was increased in the case of papers made from fibres with the highest degree of oxidation, i.e. the sheets became more sensitive to absolute changes in moisture content.
Svensson, Anna. "Nanocomposites made from nanoporous cellulose fibre". Licentiate thesis, KTH, Fiberteknologi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-103342.
Pełny tekst źródłaQC 20121011
Almgren, Karin M. "Wood-fibre composites : Stress transfer and hygroexpansion". Doctoral thesis, KTH, Träkemi och massateknologi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-12309.
Pełny tekst źródłaQC20100714
Kihlman, Martin. "Dissolution of cellulose for textile fibre applications". Licentiate thesis, Karlstads universitet, Avdelningen för kemiteknik, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-12798.
Pełny tekst źródłaCelluNova
Paterson, Daniel Thomas. "Understanding rapid dewatering of cellulose fibre suspensions". Thesis, University of British Columbia, 2016. http://hdl.handle.net/2429/58195.
Pełny tekst źródłaApplied Science, Faculty of
Mechanical Engineering, Department of
Graduate
Bergström, Roger. "Fibre flow mechanisms". Doctoral thesis, KTH, Fiber- och polymerteknik, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-240.
Pełny tekst źródłaQC 20100901
Solberg, Daniel. "Adsorption kinetics of cationic polyacrylamides on cellulose fibres and its influence on fibre flocculation". Licentiate thesis, KTH, Fibre and Polymer Technology, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-1665.
Pełny tekst źródłaThe 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 electrostaticequilibrium. 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 Healys 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.
Keywords:Adsorption, bridging, cationic polymers,cellulose fibres, electrosteric stabilisation flocculation,ionic strength, nanoparticle, polyelectrolyte, reconformation,retention aids and silica
Tawari, Akram. "Development of a cellulose acetate hollow-fine-fibre membrane". Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/4253.
Pełny tekst źródłaENGLISH ABSTRACT: The goal of this study is to produce cellulose acetate (CA) hollow-fine-fibre membranes with good water flux performance in the 95 – 96% salt retention range for brackish water desalination from first principles. First, the acceptable range of fibre dimensions was determined by means of a collapse pressure calculation using the elastic buckling pressure equation (thin shell assumption). Second, the pressure drop across the fibre wall in the hollow-fine fibre was determined by using the Hagen-Poiseuille equation, in order to determine how this would affect the chosen fibre dimensions. It was determined that the acceptable range of fibre dimensions was 222 – 247 m, and the wall thickness was 50 m. Fibres with these dimensions exhibited a high resistance to brackish water operating pressure of 20 – 25 bar, without collapse. The pressure drop calculations of these dimensions showed a sufficiently low pressure drop across the fibres. A dry-wet spinning technique was used for the preparation of the hollow-fine-fibre membranes. Hollow-fine fibres were spun using CA dissolved in a suitable solvent and non-solvent mixture comprising acetone and formamide. The effects of the dope composition and spinning parameters such as solvent to non-solvent ratio, bore fluid ratio, take-up speed, dope extrusion rate and heat treatment on the membrane morphology and performance were investigated. The spun fibres showed a good morphological structure, with no macrovoids (sponge-like structure), which is favourable for reverse osmosis (RO) applications. The hollow-fine-fibre membranes showed a good brackish water desalination performance within brackish water operating conditions. Statistical analysis was used to generate a fabrication formulation for producing cellulose acetate hollow-fine-fibre membrane for brackish water desalination with improved salt retention and flux. A three-level three-factor factorial was used to the study of the effect of spinning parameters (solvent to non-solvent ratio, bore fluid ratio and air gap distance). A regression equation was successfully established and was used to predictably produce membranes with good performance within the limits of the factors studied. RO performance of these hollow-fine-fibre membranes was good: The salt retention ranged from 96 to 98% and the permeate flux ranged from 60 to 46 L/m2.d (2 000 ppm, NaCl, 20 bar, 24 oC).
AFRIKAANSE OPSOMMING: Die studie het ten doel gehad om selluloseasetaat holveselmembrane vanaf eerste beginsels vir brakwaterontsouting te ontwikkel. Die ontsoutingsvlakke van die membrane moet tussen 95 en 96% lê met ’n aanvaarbare waterproduksievermoë. Aanvaarbare deursneë vir die holvesels is eerstens bepaal deur platval-berekeninge met behulp van die inmekaarvouvergelyking uit te voer (dunwand aanname). Hierna is drukval oor die wand van die holvesel met behulp van die Hagen-Poiseuille vergelyking bepaal ten einde vas te stel hoe dit die gekose dimensies sal beïnvloed. Daar is vasgestel dat vesel deursneë tussen 222 en 247 um met ’n 50 um wand aanvaarbaar is. Vesels met hierdie dimensies het ’n hoë weerstand teen inval getoon by brakwater opereringsdrukke tussen 20 en 25 bar. ’n Droë-nat spintegniek is in die voorbereiding van die holveselmembrane gebruik. Holvesel membrane is met ’n selluloseasetaat stroop gespin wat uit ’n oplosmiddel (asetoon) en nieoplossmiddel (formamied) bestaan het. Die effek van die spinstroop samestelling en spinparameters soos die oplosmiddel tot nieoplosmiddel verhouding, lumen-vloeistof verhouding, opneemspoed, spinstroop ekstrusie tempo en hittebehandeling op membraan morfologie en werkverrigting is ondersoek. Die gespinde vesels toon ’n sponsagtige struktuur sonder die teenwoordigheid van enige mikroleemtes wat voordelig is vir tru-osmose toepassings. Die holvesel membrane het aanvaarbare brakwater ontsoutings werkverrigting. Statistiese analise is gebruik in die generasie van produksieformulasies vir die produksie van brakwater ontsoutingsmembrane met verbeterde retensie en vloed. ’n Drie-vlak driefaktoriaal ontwerp is tydens die studie gebruik om die effek van spinparameters (oplosmiddel tot nie-oplosmiddel verhouding, lumen vloeistof verhouding, en lug-gaping) te ondersoek. ’n Regressie vergelyking is suksesvol daargestel en gebruik om voorspelbaar membrane met goeie werkverrigting binne die limiete van die studie te produseer. Die tru-osmose werkverrigting van die membrane was goed: die sout retensie het tussen 96 en 98% gelê en die permeaatvloed tussen 60 en 46 L/m2.d (2 000 ppm NaCl, 20 bar, 24oC).
Källgren, Rasmus. "Influence of level of cellulose oxidation and surface treatment on the adhesion between cellulose beads". Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-276412.
Pełny tekst źródłaMed klimatfrågans växande inverkan på både politiska beslut och hur företagen utvecklar sina produkter så läggs det allt större vikt vid att hitta miljövänliga alternativ till fossilbaserade material. Ett av de mer intressanta materialen är cellulosa vilket är världens mest naturligt förekommande polymer och som kan användas i en rad olika tillämpningar. Ett sätt att modifiera fibrerna och att ändra deras egenskaper är att använda sig av en metod som kalls Layer-by-layer (LbL) behandling där två polymerer mot motsatt laddning växelvis adsorberas till fiberytan. En annan möjlighet är att oxidera cellulosan i fibrerna så att de erhåller de en högre laddning. Detta innebär dels att fibrerna kan adsorbera en högre mängd katjoniska tillsatskemikalier samt att fibrerna sväller mera vilket innebär att de plasticeras och kan skapa starkare fogar mellan fiberytorna i torrt tillstånd vilket resulterar i starkare torra fibernätverk. Vedbaserade fibrer är dock små och inhomogena såväl kemiskt som morfologiskt vilket innebär att det är nödvändigt att använda modellsystem för att kunna klarlägga, i detalj, hur behandlade och icke behandlade ytor växelverkar med varandra på en molekylär nivå. Ett modellsystem som kan användas för att undersöka hur cellulosafibrer påverkas av att beläggas med hjälp av LbL metoden är att använda sig av sfäriska kulor tillverkade från regenererad cellulosa. I föreliggande arbete behandlades dessa kulor med polyallylaminhydroklorid (PAH) och hylauronsyra (HA) samt med PAH och alginat (Alg) innan de tilläts torka ihop och därefter utsattes för dragprovning för att klarlägga adhesionen mellan ytorna. Kulorna behandlades med fem respektive tio bilager av dessa polymerer och torkades sedan ihop på en AKD-belagd yta, för att undvika adhesion till den underliggande ytan, för att undersöka adhesionen mellan kulorna. Adhesionen ökade när de behandlades med LbL och blev högre vid adsorption av flera lager polyelektrolyter och systemet med Alg/PAH resulterade i den största ökningen. Prover med tio lager av Alg/PAH testades även efter att en lösning av kalciumklorid tillsattes under torkningen vilket resulterade i en sämre adhesion mellan kulorna.
Książki na temat "Cellulose fibre"
Vares, Sirje. Cellulose fibre concrete. Espoo, Finland: Technical Research Centre of Finland, 1997.
Znajdź pełny tekst źródłaAkbulut, Huseyin. The properties and performance of cellulose fibre reinforced stone mastic asphalt. [s.l: The Author], 1999.
Znajdź pełny tekst źródłaPlatts, R. E. Development of "stud hugger" systems for insulating walls with cellulose fibre insulation: Report for the Housing Technology Incentives Program, Canada Mortgage and Housing Corporation. Ottawa, Ont: Canada Mortgage and Housing Corporation, 1995.
Znajdź pełny tekst źródłaSfiligoj Smole, Majda, Silvo Hribernik, Manja Kurečič, Andreja Urbanek Krajnc, Tatjana Kreže i Karin Stana Kleinschek. Surface Properties of Non-conventional Cellulose Fibres. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-10407-8.
Pełny tekst źródłaKamide, Kenji. Regenerated cellulose fiber industry: A history of technological and economical advances. Fukuoka-shi, Japan: Kyushu University Press, 2006.
Znajdź pełny tekst źródłaSuleman, A. U. M. AFM studies of cellulosic fibres. Manchester: UMIST, 1996.
Znajdź pełny tekst źródłaPeltonen, Petri. Asphalt mixtures modified with tall oil pitches and cellulose fibres. Espoo, Finland: VTT, Technical Research Centre of Finland, 1992.
Znajdź pełny tekst źródłaCellulosic materials: Fibers, networks, and composites. Boston, Mass: Kluwer Academic Publishers, 2002.
Znajdź pełny tekst źródłaOhlemiller, T. J. Forced smolder propagation and the transition to flaming in cellulosic insulation. Gaithersburg, MD: U.S. Dept. of Commerce, National Bureau of Standards, 1985.
Znajdź pełny tekst źródłaHussain, A. J. Fractal simulation of material damage accumulation in cellulosic fibres. Manchester: UMIST, 1996.
Znajdź pełny tekst źródłaCzęści książek na temat "Cellulose fibre"
Rana, Sohel, Shama Parveen, Subramani Pichandi i Raul Fangueiro. "Development and Characterization of Microcrystalline Cellulose Based Novel Multi-scale Biocomposites". W Advances in Natural Fibre Composites, 159–73. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64641-1_15.
Pełny tekst źródłaNjuguna, James, Paul Wambua, Krzysztof Pielichowski i Kambiz Kayvantash. "Natural Fibre-Reinforced Polymer Composites and Nanocomposites for Automotive Applications". W Cellulose Fibers: Bio- and Nano-Polymer Composites, 661–700. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-17370-7_23.
Pełny tekst źródłaOnyianta, Amaka Joy, i Rhodri Williams. "The Use of Sedimentation for the Estimation of Aspect Ratios of Charged Cellulose Nanofibrils". W Advances in Natural Fibre Composites, 195–203. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64641-1_17.
Pełny tekst źródłaMathew, Lovely, M. K. Joshy i Rani Joseph. "Isora Fibre: A Natural Reinforcement for the Development of High Performance Engineering Materials". W Cellulose Fibers: Bio- and Nano-Polymer Composites, 291–324. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-17370-7_11.
Pełny tekst źródłade Lhoneux, B., E. Baes i T. Avella. "Ultrastructural Aspects of Fibre—Matrix Bond in Cellulose Cement Composites". W Interfaces in New Materials, 129–38. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3680-8_13.
Pełny tekst źródłaYang, Muhamad Firdaus Muhamad, Hisham Hamid i Ahmad Makarimi Abdullah. "Potential Use of Cellulose Fibre Composites in Marine Environment—A Review". W Engineering Applications for New Materials and Technologies, 25–55. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-72697-7_3.
Pełny tekst źródłaRusina, O., R. Kirmeier, A. Molinero, C. R. Rambo i H. Sieber. "Manufacturing of Highly-Porous SIC-Ceramics from SI-Filled Cellulose Fibre Papers". W Ceramic Transactions Series, 169–76. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118407820.ch16.
Pełny tekst źródłaGooch, Jan W. "Cellulose Fiber". W Encyclopedic Dictionary of Polymers, 128. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_2111.
Pełny tekst źródłaSrinivasababu, Nadendla. "Mechanical Performance of Nanoclay-Cellulose Fibre Particulate Composites Fabricated by Modified Two Stage Wet/Hand Layup Method". W Nanoclay Reinforced Polymer Composites, 239–61. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-0950-1_10.
Pełny tekst źródłaKasakov, M. Ye, L. L. Kalachyeva, Yu N. Movchan i G. M. Butyrin. "Influence of Thermal and Electrical-Chemical Treatments on Some Properties of Carbon Fibre Materials from Hydrated Cellulose". W MICC 90, 204–8. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3676-1_25.
Pełny tekst źródłaStreszczenia konferencji na temat "Cellulose fibre"
Hospodarova, Viola, Nadezda Stevulova, Vojtech Vaclavik, Tomas Dvorsky i Jaroslav Briancin. "Cellulose Fibres as a Reinforcing Element in Building Materials". W Environmental Engineering. VGTU Technika, 2017. http://dx.doi.org/10.3846/enviro.2017.104.
Pełny tekst źródłaCiambella, Jacopo, i David C. Stanier. "Orientation Effects in Short Fibre-Reinforced Elastomers". W ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-40430.
Pełny tekst źródłaNaqiya, F. M. Z., I. Ahmad i O. B. Airianah. "Resistant-hemicelluloses toward successive chemical treatment during cellulose fibre extraction". W THE 2017 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the University Kebangsaan Malaysia, Faculty of Science and Technology 2017 Postgraduate Colloquium. Author(s), 2018. http://dx.doi.org/10.1063/1.5027975.
Pełny tekst źródłaSouza, N. F., J. A. Pinheiro, N. F. Vasconcelos, M. F. Rosa, J. P. S. Morais, A. R. Cassales i M. S. M. S. Filho. "CRYSTALLOGRAPHIC CHARACTERISATION OF CELLULOSE NANOWHISKERS FROM OIL PALM FIBRE WASTE". W International Symposium on Crystallography. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/phypro-sic100-092.
Pełny tekst źródłaSaavedra Flores, Erick I., Senthil Murugan, Michael I. Friswell i Eduardo A. de Souza Neto. "Fully Coupled Three-Scale Finite Element Model for the Mechanical Response of a New Bio-Inspired Composite". W ASME 2011 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2011. http://dx.doi.org/10.1115/smasis2011-4946.
Pełny tekst źródłaCennamo, Nunzio, Carlo Trigona, Salvatore Graziani, Luigi Zeni, Francesco Arcadio, Giovanna Di Pasquale i Antonino Pollicino. "Extrinsic plasmonic optical fiber sensors based on POFs and bacterial cellulose slab waveguides". W Seventh European Workshop on Optical Fibre Sensors (EWOFS 2019), redaktorzy Kyriacos Kalli, Gilberto Brambilla i Sinead O. O'Keeffe. SPIE, 2019. http://dx.doi.org/10.1117/12.2539335.
Pełny tekst źródłaFunar-Timofei, Simona, Ludovic Kuruntzi, Walter Fabian i Daniela Ionescu. "Structure-Affinity Modeling of Azo Dye Adsorption on Cellulose Fibre by MLR". W The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01283.
Pełny tekst źródłaChan, Wei Bin, Siew Wei Phang i Li Wan Yoon. "Thermal and biodegradability study for garden waste cellulose fibre in thermoplastic starch composite". W 13TH INTERNATIONAL ENGINEERING RESEARCH CONFERENCE (13TH EURECA 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001496.
Pełny tekst źródłaKarlovits, Igor. "Lignocellulosic bio-refinery downstream products in future packaging applications". W 10th International Symposium on Graphic Engineering and Design. University of Novi Sad, Faculty of technical sciences, Department of graphic engineering and design,, 2020. http://dx.doi.org/10.24867/grid-2020-p2.
Pełny tekst źródłaMondal, Sabyasachi, Puja Agarwala, Suvankar Dutta, Vishvas Naik-Nimbalkar, Pratik Pande i Sunil Dhumal. "Cellulosic fibre drying: fundamental understanding and process modeling". W 21st International Drying Symposium. Valencia: Universitat Politècnica València, 2018. http://dx.doi.org/10.4995/ids2018.2018.7384.
Pełny tekst źródłaRaporty organizacyjne na temat "Cellulose fibre"
Kosny, Jan, David W. Yarbrough, William A. Miller, Thomas Petrie, Phillip W. Childs i Azam M. Syed. 2006/07 Field Testing of Cellulose Fiber Insulation Enhanced with Phase Change Material. Office of Scientific and Technical Information (OSTI), grudzień 2008. http://dx.doi.org/10.2172/983811.
Pełny tekst źródłaMizell, Steve A., i Craig A. Shadel. Radiological results for samples collected on paired glass- and cellulose-fiber filters at the Sandia complex, Tonopah Test Range, Nevada. Office of Scientific and Technical Information (OSTI), marzec 2016. http://dx.doi.org/10.2172/1242391.
Pełny tekst źródłaLundy, Erika L., Daniel D. Loy i Stephanie L. Hansen. Influence of Distillers Grains from a Cellulosic Ethanol Process Utilizing Corn Kernel Fiber on Nutrient Digestibility of Lambs and Steer Feedlot Performance. Ames (Iowa): Iowa State University, styczeń 2015. http://dx.doi.org/10.31274/ans_air-180814-1273.
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