Diffusion and Saponification Inside Porous Cellulose Triacetate Fibers
| Autor: | John F. Kadla, Jennifer L. Braun |
|---|---|
| Rok vydání: | 2004 |
| Předmět: |
Polymers and Plastics
Chemistry Hydrolysis Membranes Artificial Bioengineering Alkaline hydrolysis (body disposal) Cellulose acetate Diffusion Biomaterials Kinetics chemistry.chemical_compound Cellulose triacetate Reaction rate constant Reagent Polymer chemistry Materials Chemistry Fiber Solvent effects Cellulose Mathematics Saponification Nuclear chemistry |
| Zdroj: | Biomacromolecules. 6:152-160 |
| ISSN: | 1526-4602 1525-7797 |
| DOI: | 10.1021/bm0496413 |
| Popis: | Cellulose triacetate (CTA) fibers were partially hydrolyzed in 0.054 N solutions of NaOH/H(2)O and NaOMe/MeOH. The surface concentration of acetyl groups was determined using ATR-FTIR. Total acetyl content was determined by the alkaline hydrolysis method. Fiber cross-sections were stained with Congo red in order to examine the interface between reacted and unreacted material; these data were used to estimate the rate constant k and effective diffusivity D(B) for each reagent during the early stages of reaction by means of a volume-based unreacted core model. For NaOH/H(2)O, k = 0.37 L mol(-1) min(-1) and D(B) = 6.2 x 10(-7) cm(2)/sec; for NaOMe/MeOH, k = 4.0 L mol(-1) min(-1) and D(B) = 5.7 x 10(-6) cm(2)/sec. The NaOMe/MeOH reaction has a larger rate constant due to solvent effects and the greater nucleophilicity of MeO(-) as compared to OH(-); the reaction has a larger effective diffusivity because CTA swells more in MeOH than it does in water. Similarities between calculated concentration profiles for each case indicate that the relatively diffuse interface seen in fibers from the NaOMe/MeOH reaction results from factors not considered in the model; shrinkage of stained fiber cross-sections suggests that increased disruption of intermolecular forces may be the cause. |
| Databáze: | OpenAIRE |
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