Abstract
The adsorption behavior of ionized poly(acrylic acid) on tribasic calcium phosphate surfaces from aqueous solutions has been studied by Fourier transform infrared spectroscopy. Measurements included the amount adsorbed, a parameter proportional to fraction of surface-bound repeating units, and the extent of water-induced desorption. Results indicate that the cationic nature of the adsorbing surface is the main driving force for the intense and largely irreversible adsorption of the anionic polyelectrolyte. Another important factor in the adsorption behavior is the collective drag of macromolecules toward the surface through segmental interactions in solution. Collective surface migration of chains is most prominent in solutions of high concentration or molecular weight. Such adsorbates are partly desorbable and contain low fractions of surface-bound repeating units. The intensity of collective drag decreases significantly in concentrated solutions with ionization of side groups and screening of the surface potential by addition of monovalent ions to the solvating medium.
| Original language | English |
|---|---|
| Pages (from-to) | 1143-1150 |
| Number of pages | 8 |
| Journal | Macromolecules |
| Volume | 16 |
| Issue number | 7 |
| Publication status | Published - 1983 |
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ASJC Scopus subject areas
- Materials Chemistry
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Adsorption of ionizable polymers on ionic surfaces : Poly(acrylic acid). / Belton, Daniel; Stupp, Samuel I.
In: Macromolecules, Vol. 16, No. 7, 1983, p. 1143-1150.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Adsorption of ionizable polymers on ionic surfaces
T2 - Poly(acrylic acid)
AU - Belton, Daniel
AU - Stupp, Samuel I
PY - 1983
Y1 - 1983
N2 - The adsorption behavior of ionized poly(acrylic acid) on tribasic calcium phosphate surfaces from aqueous solutions has been studied by Fourier transform infrared spectroscopy. Measurements included the amount adsorbed, a parameter proportional to fraction of surface-bound repeating units, and the extent of water-induced desorption. Results indicate that the cationic nature of the adsorbing surface is the main driving force for the intense and largely irreversible adsorption of the anionic polyelectrolyte. Another important factor in the adsorption behavior is the collective drag of macromolecules toward the surface through segmental interactions in solution. Collective surface migration of chains is most prominent in solutions of high concentration or molecular weight. Such adsorbates are partly desorbable and contain low fractions of surface-bound repeating units. The intensity of collective drag decreases significantly in concentrated solutions with ionization of side groups and screening of the surface potential by addition of monovalent ions to the solvating medium.
AB - The adsorption behavior of ionized poly(acrylic acid) on tribasic calcium phosphate surfaces from aqueous solutions has been studied by Fourier transform infrared spectroscopy. Measurements included the amount adsorbed, a parameter proportional to fraction of surface-bound repeating units, and the extent of water-induced desorption. Results indicate that the cationic nature of the adsorbing surface is the main driving force for the intense and largely irreversible adsorption of the anionic polyelectrolyte. Another important factor in the adsorption behavior is the collective drag of macromolecules toward the surface through segmental interactions in solution. Collective surface migration of chains is most prominent in solutions of high concentration or molecular weight. Such adsorbates are partly desorbable and contain low fractions of surface-bound repeating units. The intensity of collective drag decreases significantly in concentrated solutions with ionization of side groups and screening of the surface potential by addition of monovalent ions to the solvating medium.
UR - http://www.scopus.com/inward/record.url?scp=0001005388&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0001005388&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0001005388
VL - 16
SP - 1143
EP - 1150
JO - Macromolecules
JF - Macromolecules
SN - 0024-9297
IS - 7
ER -