Effects of Non-Ionic Micelles on the Acid-Base Equilibria of a Weak Polyelectrolyte

被引:5
|
作者
Yekymov, Evgenee [1 ]
Attia, David [1 ]
Levi-Kalisman, Yael [2 ,3 ]
Bitton, Ronit [1 ,4 ]
Yerushalmi-Rozen, Rachel [1 ,4 ]
机构
[1] Ben Gurion Univ Negev, Dept Chem Engn, IL-84105 Beer Sheva, Israel
[2] Hebrew Univ Jerusalem, Ctr Nanosci & Nanotechnol, IL-91904 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Inst Life Sci, IL-91904 Jerusalem, Israel
[4] Ben Gurion Univ Negev, Ilse Katz Inst Nanosci & Technol, IL-84105 Beer Sheva, Israel
基金
以色列科学基金会;
关键词
polyacrylic acid; PAA; weak polyelectrolytes; WPEs; acid base; equilibrium; pKa; pH; excluded volume; surfactant; Brij-S20; F108; F127; X-RAY-SCATTERING; POLY(ACRYLIC ACID); AQUEOUS-SOLUTION; PH; BEHAVIOR; ADSORPTION; SOLUBILIZATION; TEMPERATURE; COPOLYMERS; COMPLEXES;
D O I
10.3390/polym14091926
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Weak polyelectrolytes (WPEs) are widely used as pH-responsive materials, pH modulators and charge regulators in biomedical and technological applications that involve multi-component fluid environments. In these complex fluids, coupling between (often weak) interactions induced by micelles, nanoparticles and molecular aggregates modify the pKa as compared to that measured in single component solutions. Here we investigated the effect of coupling between hydrogen bonding and excluded volume interactions on the titration curves and pKa of polyacrylic acid (PAA) in solutions comprising PEO-based micelles (Pluronics and Brij-S20) of different size and volume fraction. Titration experiments of dilute, salt-free solutions of PAA (5 kDa, 30 kDa and 100 kDa) at low degree of polymer ionization (alpha < 0.25) drive spatial re-organization of the system, reduce the degree of ionization and consequentially increase the pKa by up to similar to 0.7 units. These findings indicate that the actual degree of ionization of WPEs measured in complex fluids is significantly lower (at a given pH) than that measured in single-component solutions.
引用
收藏
页数:17
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