Die Festigkeitseigenschaften des Papiers hängen vom Gehalt und der Verteilung der Hemicellulosen über den Querschnitt der Faserwand ab. Hemicellulosen werden durch verschiedene Bleichverfahren unterschiedlich stark angegriffen und herausgelöst. Durch Untersuchungen an einem Fichtensulfitzellstoff ist es gelungen, die Auswirkungen einzelner Bleichstufen [Peroxidverstärkte Sauerstoffstufe (EOP), Ozonstufe (Z) und Peressigsäurestufe (PAA)] und Bleichsequenzen (EOP-Z-P, EOP-PAA-P) auf Faseroberfläche, Hemicellulosenzusammensetzung und -verteilung sowie auf die optischen und mechanischen Eigenschaften des daraus gebildeten Papiers aufzuzeigen. Um die Verteilung der Hemicellulosen über den Querschnitt der Faser zu beschreiben, wird das Verfahren des chemischen Abschälens verwendet und schrittweise die Faserwand entfernt. Der gebleichte bzw. abgeschälte Zellstoff wird rasterelektronenmikroskopisch untersucht, hydrolysiert und anschließend die Hemicellulosenzusammensetzung quantitativ mittels Hochdruckflüssigkeitschromatographie (HPLC) unter Nutzung eines Flüssigkeitsmassenspektrometers (LCMS) als Detektor bestimmt. Zusätzlich erfolgt die Bestimmung der Papiereigenschaften. Diese Untersuchungen bestätigen, dass die verschiedenen Hemicellulosengehalte nach den Bleichstufen Unterschiede bei den Festigkeitseigenschaften bewirken. Die Untersuchungen zeigen den positiven Effekt der Peressigsäurestufe für die Papierherstellung im direkten Vergleich zur Ozonstufe. Zusätzlich wurde auch der Einfluss des Aufschlusses geprüft. Hierzu wurden die endgebleichten Sulfitzellstoffe mit einem endgebleichten Sulfatzellstoff verglichen. / The mechanical strength of paper pulp depends strongly on the hemicellulose content and the hemicellulose distribution across the cell wall layers. Hemicelluloses get differently attacked and dissolved by different bleaching methods. The investigations with a paper grade sulphite pulp show the influence of the separate bleaching steps [hydrogen peroxide reinforced oxygen stage (EOP), ozone (Z) und peracetic acid (PAA)] and bleaching sequences (EOP-Z-P, EOP-PAA-P) of the fibre surface, hemicellulose content and distribution as well as the optical and mechanical characteristics of paper. To describe the hemicellulose distribution across the cell wall layers a procedure of a precise chemical peeling was used in order to remove stepwise the cell wall. The bleached and peeled pulp was investigated by scanning electronic microscope (SEM) to get more information about the penetration of the bleaching chemicals into the fibre surface. The hemicelluloses were determined by high performance liquid chromatography (HPLC) using a liquid chromatography mass spectrometer (LCMS) after hydrolysing polysaccharides to monosaccharides. In addition to this paper properties were analysed. This research confirms the effect of different hemicellulose compositions of the mechanical strength. The analyses represent the positive effect for paper production of the peracetic acid step in contrast to the ozone step. Additional the influence of the pulping process was determined by a sulphate pulp comparing with the sulphite pulp.

Die Festigkeitseigenschaften des Papiers hängen vom Gehalt und der Verteilung der Hemicellulosen über den Querschnitt der Faserwand ab. Hemicellulosen werden durch verschiedene Bleichverfahren unterschiedlich stark angegriffen und herausgelöst. Durch Untersuchungen an einem Fichtensulfitzellstoff ist es gelungen, die Auswirkungen einzelner Bleichstufen [Peroxidverstärkte Sauerstoffstufe (EOP), Ozonstufe (Z) und Peressigsäurestufe (PAA)] und Bleichsequenzen (EOP-Z-P, EOP-PAA-P) auf Faseroberfläche, Hemicellulosenzusammensetzung und -verteilung sowie auf die optischen und mechanischen Eigenschaften des daraus gebildeten Papiers aufzuzeigen. Um die Verteilung der Hemicellulosen über den Querschnitt der Faser zu beschreiben, wird das Verfahren des chemischen Abschälens verwendet und schrittweise die Faserwand entfernt. Der gebleichte bzw. abgeschälte Zellstoff wird rasterelektronenmikroskopisch untersucht, hydrolysiert und anschließend die Hemicellulosenzusammensetzung quantitativ mittels Hochdruckflüssigkeitschromatographie (HPLC) unter Nutzung eines Flüssigkeitsmassenspektrometers (LCMS) als Detektor bestimmt. Zusätzlich erfolgt die Bestimmung der Papiereigenschaften. Diese Untersuchungen bestätigen, dass die verschiedenen Hemicellulosengehalte nach den Bleichstufen Unterschiede bei den Festigkeitseigenschaften bewirken. Die Untersuchungen zeigen den positiven Effekt der Peressigsäurestufe für die Papierherstellung im direkten Vergleich zur Ozonstufe. Zusätzlich wurde auch der Einfluss des Aufschlusses geprüft. Hierzu wurden die endgebleichten Sulfitzellstoffe mit einem endgebleichten Sulfatzellstoff verglichen. / The mechanical strength of paper pulp depends strongly on the hemicellulose content and the hemicellulose distribution across the cell wall layers. Hemicelluloses get differently attacked and dissolved by different bleaching methods. The investigations with a paper grade sulphite pulp show the influence of the separate bleaching steps [hydrogen peroxide reinforced oxygen stage (EOP), ozone (Z) und peracetic acid (PAA)] and bleaching sequences (EOP-Z-P, EOP-PAA-P) of the fibre surface, hemicellulose content and distribution as well as the optical and mechanical characteristics of paper. To describe the hemicellulose distribution across the cell wall layers a procedure of a precise chemical peeling was used in order to remove stepwise the cell wall. The bleached and peeled pulp was investigated by scanning electronic microscope (SEM) to get more information about the penetration of the bleaching chemicals into the fibre surface. The hemicelluloses were determined by high performance liquid chromatography (HPLC) using a liquid chromatography mass spectrometer (LCMS) after hydrolysing polysaccharides to monosaccharides. In addition to this paper properties were analysed. This research confirms the effect of different hemicellulose compositions of the mechanical strength. The analyses represent the positive effect for paper production of the peracetic acid step in contrast to the ozone step. Additional the influence of the pulping process was determined by a sulphate pulp comparing with the sulphite pulp.

Dynamic (or 2D) FT-IR spectroscopy in combination withpolarized IR irradiation has been used in this work to studywood polymer orientation and interactions on theultrastructural level in wood fibers in the native state aswell as the effects of different pulping processes. The woodpolymer interactions were studied under both dry and humidconditions. The matrix of lignin and hemicelluloses located between thewell-ordered cellulose fibrils in the wood cell wall of sprucewas here shown to be more highly ordered than has earlier beenrevealed. It was confirmed that glucomannan is orientedparallel to the cellulose fibrils and is highly coupled to it.The lignin was also shown to have a main orientation in thestructure although this is probably not as strong as that ofglucomannan. The orientation of the lignin may derive from thefact that the polysaccharides act as templates during thelignification of the cell wall. This organization implies thatnot only the cellulose but also the lignin and thehemicelluloses have different mechanical properties in thelongitudinal and cross-fiber directions. The ability to gain molecular information on the stresstransfer in polymers with dynamic FT-IR spectroscopy made itpossible to verify experimentally earlier molecularcalculations on the stress transfer within the cellulose chain.It was also possible to show, on the molecular level, thedominant importance of the cellulose fibrils for the stresstransfer in the longitudinal direction of pulp fibers,including lignin-rich mechanical pulp fibers. The glucomannanof softwood fibers was also shown to participate in the stresstransfer in the fiber direction indicating a close associationwith the cellulose, whereas the xylan showed no dynamicresponse. Already under dry conditions, the lignin was shown tohave a more viscoelastic response than the polysaccharidesduring the loading of pulp fibers and it was thus able to moveindependently of the cellulose. The enhanced spectral resolution obtained with dynamic FT-IRspectroscopy made it possible to study the crystalstructure/chain order of cellulose in pulp fibers. Thepossibility of following changes in the relative cellulose Iallomorph composition of pulp fibers was demonstrated for somechemical pulps. Dynamic FT-IR experiments under humid conditions and ofelevated temperatures made it possible to study the softeningof the biopolymers in their native environment. This was alsodemonstrated for some different pulps, and this may be apromising tool for obtaining viscoelastic information on themolecular level in composite systems such as wood fibers. <b>Keywords:</b>cellulose, cooperation, crystallinity, dynamictest, glucomannan, hardwood, holocellulose, humidity, infraredspectroscopy, kraft pulp, lignin, mechanical pulp, orientation,polarised light, softwood, strain, sulphite pulp,viscoelasticity, xylan

<p>Dynamic (or 2D) FT-IR spectroscopy in combination withpolarized IR irradiation has been used in this work to studywood polymer orientation and interactions on theultrastructural level in wood fibers in the native state aswell as the effects of different pulping processes. The woodpolymer interactions were studied under both dry and humidconditions.</p><p>The matrix of lignin and hemicelluloses located between thewell-ordered cellulose fibrils in the wood cell wall of sprucewas here shown to be more highly ordered than has earlier beenrevealed. It was confirmed that glucomannan is orientedparallel to the cellulose fibrils and is highly coupled to it.The lignin was also shown to have a main orientation in thestructure although this is probably not as strong as that ofglucomannan. The orientation of the lignin may derive from thefact that the polysaccharides act as templates during thelignification of the cell wall. This organization implies thatnot only the cellulose but also the lignin and thehemicelluloses have different mechanical properties in thelongitudinal and cross-fiber directions.</p><p>The ability to gain molecular information on the stresstransfer in polymers with dynamic FT-IR spectroscopy made itpossible to verify experimentally earlier molecularcalculations on the stress transfer within the cellulose chain.It was also possible to show, on the molecular level, thedominant importance of the cellulose fibrils for the stresstransfer in the longitudinal direction of pulp fibers,including lignin-rich mechanical pulp fibers. The glucomannanof softwood fibers was also shown to participate in the stresstransfer in the fiber direction indicating a close associationwith the cellulose, whereas the xylan showed no dynamicresponse. Already under dry conditions, the lignin was shown tohave a more viscoelastic response than the polysaccharidesduring the loading of pulp fibers and it was thus able to moveindependently of the cellulose.</p><p>The enhanced spectral resolution obtained with dynamic FT-IRspectroscopy made it possible to study the crystalstructure/chain order of cellulose in pulp fibers. Thepossibility of following changes in the relative cellulose Iallomorph composition of pulp fibers was demonstrated for somechemical pulps.</p><p>Dynamic FT-IR experiments under humid conditions and ofelevated temperatures made it possible to study the softeningof the biopolymers in their native environment. This was alsodemonstrated for some different pulps, and this may be apromising tool for obtaining viscoelastic information on themolecular level in composite systems such as wood fibers.</p><p><b>Keywords:</b>cellulose, cooperation, crystallinity, dynamictest, glucomannan, hardwood, holocellulose, humidity, infraredspectroscopy, kraft pulp, lignin, mechanical pulp, orientation,polarised light, softwood, strain, sulphite pulp,viscoelasticity, xylan</p>