TY - JOUR
T1 - Significance of xylan on the stability and water interactions of cellulosic nanofibrils
AU - Tenhunen, Tiia Maria
AU - Peresin, Maria Soledad
AU - Penttilä, Paavo A.
AU - Pere, Jaakko
AU - Serimaa, Ritva
AU - Tammelin, Tekla
PY - 2014/1/1
Y1 - 2014/1/1
N2 - In this paper, the significance of xylan on the behaviour of kraft birch pulp based nanofibrillated cellulose (CNF) is discussed. The influence of CNF xylan content on fibril morphology, charge and stability as well as on the film formation ability was investigated, and the features detected on nanoscale and on macroscale are compared. In addition to this, the ability of fibrils to uptake water molecules were investigated by bulk and surface sensitive methods which are dynamic water sorption analysis (DVS) and quartz crystal microbalance with dissipation monitoring (QCM-D) equipped with the humidity module, respectively. Surface xylan plays a significant role as an electrosteric stabilizer in dilute CNF dispersions when the surface forces are dominant whereas the removal of xylan drastically changes the CNF dispersion properties. The settling of the unstable CNF dispersions displays behaviour which is typical for hindered sedimentation. When considering thin nanoscale layers of CNF, nanofibrillated cellulosic materials with high content of surface xylan has somewhat higher ability to bind water molecules. However, it seems that in more concentrated CNF dispersions where the fibrillar network itself plays also a decisive role, especially with respect to film formation ability, the impact of xylan diminishes. Solvent cast macroscale CNF films are still enough dense to maintain good oxygen barrier performance at higher humid conditions although agglomeration tendency of fibrils is higher due to the excessive xylan removal. These findings are of high relevance when considering nanocellulosic materials, especially in the form of gels and films, as templates for high added value material solutions.
AB - In this paper, the significance of xylan on the behaviour of kraft birch pulp based nanofibrillated cellulose (CNF) is discussed. The influence of CNF xylan content on fibril morphology, charge and stability as well as on the film formation ability was investigated, and the features detected on nanoscale and on macroscale are compared. In addition to this, the ability of fibrils to uptake water molecules were investigated by bulk and surface sensitive methods which are dynamic water sorption analysis (DVS) and quartz crystal microbalance with dissipation monitoring (QCM-D) equipped with the humidity module, respectively. Surface xylan plays a significant role as an electrosteric stabilizer in dilute CNF dispersions when the surface forces are dominant whereas the removal of xylan drastically changes the CNF dispersion properties. The settling of the unstable CNF dispersions displays behaviour which is typical for hindered sedimentation. When considering thin nanoscale layers of CNF, nanofibrillated cellulosic materials with high content of surface xylan has somewhat higher ability to bind water molecules. However, it seems that in more concentrated CNF dispersions where the fibrillar network itself plays also a decisive role, especially with respect to film formation ability, the impact of xylan diminishes. Solvent cast macroscale CNF films are still enough dense to maintain good oxygen barrier performance at higher humid conditions although agglomeration tendency of fibrils is higher due to the excessive xylan removal. These findings are of high relevance when considering nanocellulosic materials, especially in the form of gels and films, as templates for high added value material solutions.
KW - Cellulose nanofibrils
KW - Electrosteric stability
KW - Films
KW - Oxygen barrier
KW - Water interactions
KW - Xylan
UR - http://www.scopus.com/inward/record.url?scp=84912565445&partnerID=8YFLogxK
U2 - 10.1016/j.reactfunctpolym.2014.08.011
DO - 10.1016/j.reactfunctpolym.2014.08.011
M3 - Article
AN - SCOPUS:84912565445
SN - 1381-5148
VL - 85
SP - 157
EP - 166
JO - Reactive and Functional Polymers
JF - Reactive and Functional Polymers
ER -