Enzymatic hydrolysis combined with mechanical shearing and high-pressure homogenization for nanoscale cellulose fibrils and strong gels

被引:1497
作者
Paakko, M.
Ankerfors, M.
Kosonen, H.
Nykanen, A.
Ahola, S.
Osterberg, M.
Ruokolainen, J.
Laine, J.
Larsson, P. T.
Ikkala, O.
Lindstrom, T.
机构
[1] Aalto Univ, Lab Opt & Mol Mat, Dept Engn Phys & Mat, FIN-02015 Espoo, Finland
[2] Aalto Univ, Ctr New Mat, FIN-02015 Espoo, Finland
[3] STFI Packforsk AB, SE-11486 Stockholm, Sweden
[4] KTH, Royal Inst Technol, Dept Fibre & Polymer Technol, Stockholm, Sweden
[5] Trinity Coll Dublin, Dept Phys, Dublin, Ireland
[6] Aalto Univ, Dept Forest Prod Technol, Lab Forest Prod Chem, FIN-02015 Espoo, Finland
关键词
D O I
10.1021/bm061215p
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Toward exploiting the attractive mechanical properties of cellulose I nanoelements, a novel route is demonstrated, which combines enzymatic hydrolysis and mechanical shearing. Previously, an aggressive acid hydrolysis and sonication of cellulose I containing fibers was shown to lead to a network of weakly hydrogen-bonded rodlike cellulose elements typically with a low aspect ratio. On the other hand, high mechanical shearing resulted in longer and entangled nanoscale cellulose elements leading to stronger networks and gels. Nevertheless, a widespread use of the latter concept has been hindered because of lack of feasible methods of preparation, suggesting a combination of mild hydrolysis and shearing to disintegrate cellulose I containing fibers into high aspect ratio cellulose I nanoscale elements. In this work, mild enzymatic hydrolysis has been introduced and combined with mechanical shearing and a high-pressure homogenization, leading to a controlled fibrillation down to nanoscale and a network of long and highly entangled cellulose I elements. The resulting strong aqueous gels exhibit more than 5 orders of magnitude tunable storage modulus G' upon changing the concentration. Cryotransmission electron microscopy, atomic force microscopy, and cross-polarization/magic-angle spinning (CP/MAS) C-13 NMR suggest that the cellulose I structural elements obtained are dominated by two fractions, one with lateral dimension of 5-6 nm and one with lateral dimensions of about 10-20 nm. The thicker diameter regions may act as the junction zones for the networks. The resulting material will herein be referred to as MFC (microfibrillated cellulose). Dynamical rheology showed that the aqueous suspensions behaved as gels in the whole investigated concentration range 0.125-5.9% w/w, G' ranging from 1.5 Pa to 10(5) Pa. The maximum G' was high, about 2 orders of magnitude larger than typically observed for the corresponding nonentangled low aspect ratio cellulose I gels, and G' scales with concentration with the power of approximately three. The described preparation method of MFC allows control over the final properties that opens novel applications in materials science, for example, as reinforcement in composites and as templates for surface modification.
引用
收藏
页码:1934 / 1941
页数:8
相关论文
共 47 条
  • [1] [Anonymous], CHEM PHYS NETWORKS F
  • [2] Flow properties of microcrystalline cellulose suspension prepared by acid treatment of native cellulose
    Araki, J
    Wada, M
    Kuga, S
    Okano, T
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1998, 142 (01) : 75 - 82
  • [3] ATALLA RH, 1984, SCIENCE, V223, P283, DOI 10.1126/science.223.4633.283
  • [4] ATALLA RH, 1985, SCIENCE, V227, P79, DOI 10.1126/science.227.4682.79-a
  • [5] HYDROLYSIS AND CRYSTALLIZATION OF CELLULOSE
    BATTISTA, OA
    [J]. INDUSTRIAL AND ENGINEERING CHEMISTRY, 1950, 42 (03): : 502 - 507
  • [6] BATTISTA OA, 1975, MICROCRYSTAL POLYMER
  • [7] Shear Dynamics of Aqueous Suspensions of Cellulose Whiskers
    Bercea, M
    Navard, P
    [J]. MACROMOLECULES, 2000, 33 (16) : 6011 - 6016
  • [8] Berglund L, 2005, NATURAL FIBERS, BIOPOLYMERS, AND BIOCOMPOSITES, P807
  • [9] CAWS Peter., 1988, STRUCTURALISM ART IN
  • [10] Daoud M.M., 1999, SOFT MATTER PHYS