1977
DOI: 10.1147/rd.212.0131
|View full text |Cite
|
Sign up to set email alerts
|

Model for the Kinematics of Polymer Dissolution

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
56
0
1

Year Published

1999
1999
2011
2011

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 90 publications
(59 citation statements)
references
References 2 publications
2
56
0
1
Order By: Relevance
“…Tu and Ouano [83] proposed one of the first models for polymer dissolution, assuming Fickian solvent diffusion into the polymer followed by the establishment of two distinct boundaries characterized by sharp changes in the concentration of the solvent. They also assumed that the conditions of constant chain disassociation concentration and rate are established immediately upon wetting the polymer surface and that the solvent and the polymer are incompressible.…”
Section: The Multi-phase Stefan Problemmentioning
confidence: 99%
See 1 more Smart Citation
“…Tu and Ouano [83] proposed one of the first models for polymer dissolution, assuming Fickian solvent diffusion into the polymer followed by the establishment of two distinct boundaries characterized by sharp changes in the concentration of the solvent. They also assumed that the conditions of constant chain disassociation concentration and rate are established immediately upon wetting the polymer surface and that the solvent and the polymer are incompressible.…”
Section: The Multi-phase Stefan Problemmentioning
confidence: 99%
“…Experimental data from the literature [83] was compared with the model predictions with good results.…”
Section: External Mass Transfer Model Imentioning
confidence: 99%
“…Equations (3.12)-(3.13) show explicitly how the flux of drug from the polymer ball is O(1) and the normalized drug release is O(t) in the small-time limit, and the effect the kinetic parameter μ has on these processes. In particular, the kinetic boundary condition (2.9) (which leads to the so-called Case II diffusion of solvent through the polymer) dictates the scalings of drug release for small time, and without this empirical law the time-dependence would be qualitatively different (as in [26,39,41,51,52], for example). Clearly (3.12)-(3.13) break down in the limit μ → 0 + , and in fact (3.11)-(3.13) are valid only for t = O(μ 2 ) in this limit (see the related discussion in section 2.3).…”
Section: Asymptotic Limitsmentioning
confidence: 99%
“…There exists a number of mathematical models for the above processes, including the early studies [2,21,39,26,51,52] and good reviews by [37,38]. Here we are interested in those mathematical models for which the glassy-rubbery inter-face is described by a moving boundary whose kinetics is governed by an empirical law that relates the concentration of solvent there to the velocity of the interface.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation