4.7 Article

Electrospun cellulose acetate fibers: effect of solvent system on morphology and fiber diameter

Journal

CELLULOSE
Volume 14, Issue 6, Pages 563-575

Publisher

SPRINGER
DOI: 10.1007/s10570-007-9113-4

Keywords

electrospinning; ultrafine fibers; cellulose acetate; solvent

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This paper reports an investigation of the effects of solvent system, solution concentration, and applied electrostatic field strength (EFS) on the morphological appearance and/or size of as-spun cellulose acetate (CA) products. The single-solvent systems were acetone, chloroform, N,N -dimethylformamide (DMF), dichloromethane (DCM), methanol (MeOH), formic acid, and pyridine. The mixed-solvent systems were acetone-DMAc, chloroform-MeOH, and DCM-MeOH. Chloroform, DMF, DCM, MeOH, formic acid, and pyridine were able to dissolve CA, forming clear solutions (at 5% w/v), but electrospinning of these solutions produced mainly discrete beads. In contrast, electrospinning of the solution of CA in acetone produced short and beaded fibers. At the same solution concentration of 5% (w/v) electrospinning of the CA solutions was improved by addition of MeOH to either chloroform or DCM. For all the solvent systems investigated smooth fibers were obtained from 16% (w/v) CA solutions in 1:1, 2:1, and 3:1 (v/v) acetone-DMAc, 14-20% (w/v) CA solutions in 2:1 (v/v) acetone-DMAc, and 8-12% (w/v) CA solutions in 4:1 (v/v) DCM-MeOH. For the as-spun fibers from CA solutions in acetone-DMAc the average diameter ranged between 0.14 and 0.37 mu m whereas for the fibers from solutions in DCM-MeOH it ranged between 0.48 and 1.58 mu m. After submersion in distilled water for 24 h the as-spun CA fibers swelled appreciably (i.e. from 620 to 1110%) but the physical integrity of the fibrous structure remained intact.

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