Wet Spinning of Chitosan Fibers: Effect of Sodium Dodecyl Sulfate Adsorption and Enhanced Dope Temperature

被引:28
作者
Nechyporchuk, Oleksandr [1 ]
Nilsson, Ting Yang [1 ]
Ulmefors, Hanna [1 ]
Kohnke, Tobias [1 ]
机构
[1] RISE Res Inst Sweden, SE-43122 Molndal, Sweden
来源
ACS APPLIED POLYMER MATERIALS | 2020年 / 2卷 / 09期
关键词
chitosan; fibers; fiber formation; fiber spinning; wet spinning; drawing; CELLULOSE NANOCRYSTALS; CHITIN; NANOCELLULOSE; MEMBRANES; FILMS;
D O I
10.1021/acsapm.0c00562
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Production of fibers from nonthermoplastic polymers, such as chitosan, usually requires dissolution with subsequent fiber formation, for instance, via coagulation. Good fiber-forming properties enable simultaneous spinning of multiple fibers into a yarn, which is one of the prerequisites for process scalability. Here, we report a multifilament wet-spinning process that eliminates the use of such volatile organic compounds as methanol and acetone, enhances fiber formation, and allows producing continuous well-separated chitosan fibers after drying. This is achieved by (i) solidification of the extruded solution by alkali and sodium acetate in the coagulation bath and (ii) further stabilization of the fibers by adsorbing the anionic surfactant, sodium dodecyl sulfate. The obtained fibers have a circular cross section and smooth surface. We demonstrate that it is possible to increase fiber breaking tenacity and Young's modulus by applying stretching (draw ratios up to 1.77) or by incorporating cellulose nanofibrils (CNFs, up to 4 wt % based on chitosan) in the spinning solutions. However, the limitation of increased viscosity when adding CNF is needed to be overcome for possible higher reinforcement effects. We demonstrate that fiber breaking tenacity, Young's modulus, and elongation at break can be enhanced even further by increasing the spin dope temperature from 22 to 60 degrees C, with simultaneously increasing the spin dope solid content to keep the same dope viscosity. The fibers with a maximum breaking tenacity of ca. 10 cN/tex at an elongation at break of ca. 7.5% were obtained.
引用
收藏
页码:3867 / 3875
页数:9
相关论文
共 61 条
  • [1] Agboh OC, 1997, POLYM ADVAN TECHNOL, V8, P355, DOI 10.1002/(SICI)1099-1581(199706)8:6<355::AID-PAT651>3.3.CO
  • [2] 2-K
  • [3] Chitosan as biomaterial in drug delivery and tissue engineering
    Ahsan, Saad M.
    Thomas, Mathai
    Reddy, Kranthi K.
    Sooraparaju, Sujata Gopal
    Asthana, Amit
    Bhatnagar, Ira
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 110 : 97 - 109
  • [4] Impact of the wet spinning parameters on the alpaca-based polyacrylonitrile composite fibers: Morphology and enhanced mechanical properties study
    Al Faruque, Md Abdullah
    Remadevi, Rechana
    Razal, Joselito M.
    Naebe, Maryam
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2020, 137 (41)
  • [5] Self-Organized Films from Cellulose I Nanofibrils Using the Layer-by-Layer Technique
    Aulin, Christian
    Johansson, Erik
    Wagberg, Lars
    Lindstrom, Tom
    [J]. BIOMACROMOLECULES, 2010, 11 (04) : 872 - 882
  • [6] Nanocellulose Reinforced Chitosan Composite Films as Affected by Nanofiller Loading and Plasticizer Content
    Azeredo, Henriette M. C.
    Mattoso, Luiz Henrique C.
    Avena-Bustillos, Roberto J.
    Ceotto Filho, Gino
    Munford, Maximiliano L.
    Wood, Delilalh
    McHugh, Tara H.
    [J]. JOURNAL OF FOOD SCIENCE, 2010, 75 (01) : N1 - N7
  • [7] Formation of an ordered nanostructure in surfactant-polyelectrolyte complexes formed by interfacial diffusion
    Babak, VG
    Merkovich, EA
    Desbrières, J
    Rinaudo, M
    [J]. POLYMER BULLETIN, 2000, 45 (01) : 77 - 81
  • [8] Electrospun chitosan-based nanofibers and their cellular compatibility
    Bhattarai, N
    Edmondson, D
    Veiseh, O
    Matsen, FA
    Zhang, MQ
    [J]. BIOMATERIALS, 2005, 26 (31) : 6176 - 6184
  • [9] Carraher C.E., 2017, Congressional Testimony: BOP Director Charles E. Samuels, Jr., P92
  • [10] Chaturvedi V., 2010, INT J APPL BIOL PHAR, V1, P630