Adhesion to wet cellulose – Comparing adhesive layer-by-layer assembly to coating polyelectrolyte complex suspensions 2nd ICC 2007, Tokyo, Japan, October 25–29, 2007

Holzforschung ◽  
2009 ◽  
Vol 63 (1) ◽  
Author(s):  
Xianhua Feng ◽  
Dan Zhang ◽  
Robert Pelton

Abstract Polyelectrolyte complexes are routinely used as adhesives to strengthen fiber-fiber contacts in paper. This work evaluates different approaches to putting the polyelectrolyte complexes into the adhesive joint. Instead of conventional wet paper mechanical testing, a wet cellulose film delamination technique was employed permitting direct comparison of different approaches to applying the polymeric adhesive to the cellulose-cellulose joint. The adhesion strengths of layer-by-layer polyelectrolyte complexes assembled on wet cellulose films and the adhesion strengths of the corresponding polyelectrolyte complex coated on wet cellulose films are compared. The wet adhesion strengths were measured by peel delamination. The polyelectrolyte complexes were based on mixtures of cationic polyvinylamine (PVAm) and anionic carboxymethyl cellulose (CMC). The layer-by-layer assemblies of PVAm and CMC yielded stronger wet adhesion than did coated films of the corresponding colloidal complexes or pure PVAm at the same coverage (mass of polymer/joint area). The role of CMC was to give ionic crosslinks with PVAm which increase the cohesive strength of thick PVAm layers. PVAm gives much stronger wet adhesion to cellulose compared to the oxidized silicon wafer surfaces. It is proposed that imine and aminal bonds can form between the polyamine and hemiacetals in the regenerated cellulose films which cannot form with silica.

2019 ◽  
Vol 9 (9) ◽  
pp. 1750 ◽  
Author(s):  
Yao-Hsuan Tseng ◽  
Yu-Yin Lee ◽  
Shih-Hsun Chen

In this work, several kinds of quaternary ammonium-based room-temperature ionic liquids (QA RTILs) are synthesized by alkylation and ion-exchange reactions for the rapid dissolution of cellulose. The applications of cellulose materials have been limited due to their poor solubility in conventional organic solvents, because of a high degree of structural regularity and a large number of hydrogen bonds. The prepared ionic liquids were identified by nuclear magnetic resonance, elemental analysis, and liquid chromatography-mass spectrometry. The results indicated that N,N,N-triethylhexan-1-aminium acetate (N6222OAc), tetrahexylammonium acetate (N6666OAc), and N,N,N,N′,N′,N′-hexaethyldecane-1,10-diaminium acetate (C10(N222OAc)2) exhibited good cellulose-dissolution without any pretreatment. The regenerated cellulose films with a low degree of crystallization of the cellulose II phase were also prepared easily in this process using N6222OAc due to its polar and small cation. These QA RTILs can be used as non-derivatizing solvents for cellulose and can also be easily recycled because of their thermostable and nonvolatile properties.


1969 ◽  
Vol 7 (2) ◽  
pp. 325-355 ◽  
Author(s):  
Shunji Nomura ◽  
Sueo Kawabata ◽  
Hiromichi Kawai ◽  
Yutaka Yamaguchi ◽  
Akio Fukushima ◽  
...  

2013 ◽  
Vol 830 ◽  
pp. 163-166 ◽  
Author(s):  
Ri Na Wu ◽  
Hu Zhu ◽  
Bei Hai He

Dissolution of absorbent cotton (DP above 4000) using ionic liquids as solvent and regeneration was investigated. The results show that 1-ally-3-methylimidazolium chloride (AMIMCl) was a good solvent to dissolve absorbent cotton and a solution of 3 wt% can be reached in 18 min at 120°C. Besides, as the dissolving temperature increased the time needed for the cotton linters to dissolve decreased. The physic-chemical properties of the regenerated cellulose films were also characterized by XRD, FTIR and TGA analysis.


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