Search results for "polyelectrolyte"

1995

About 340 g of a cycloaliphatic ionene (see formula given in the introduction) were fractionated by a continuous countercurrent extraction method (CPF). The efficiency of the separation was checked by viscometry and gel permeation chromatography (GPC). Ten different fractions with number average molecular masses between 16 000 and 29 000 D were obtained and their glass transition temperatures T g determined by differential scanning calorimetry (DSC) for their bromide and tetrafluoroborate salts. No molecular weight dependence of T g was found, in contrast to recently reported results with aliphatic ionenes, where - in case of the bromide - T g increases with rising molecular weight.

Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Mobile supported monolayers of ionic amphiphiles: variation of domain morphology via preadsorbed polyelectrolytes

1992

Advanced Functional Structures Based on Interpolyelectrolyte Complexes

2013

This review considers interpolyelectrolyte complexes, with a particular emphasis on advanced macromolecular co-assemblies based on polyionic species with nonlinear topology and on polymer–inorganic hybrids formed by interpolyelectrolyte complexes containing metal ions and/or metal nanoparticles.

Modelling of natural and synthetic polyelectrolyte interactions in natural waters.

2006

In this paper SIT and Pitzer models are used for the first time to describe the interactions of natural and synthetic polyelectrolytes in natural waters. Measurements were made potentiometrically at 25 °C in single electrolyte media, such as Et4NI and NaCl (for fulvic acid 0.1 < I /mol L− 1 < 0.75), and in a multi-component medium simulating the composition of natural waters at a wide range of salinities (for fulvic and alginic acids: 5 < S < 45) with particular reference to sea water [Synthetic Sea Water for Equilibrium studies, SSWE]. In order to simplify calculations, SSWE was considered to be a “single salt” BA, with cation B and anion A representing all the major cations (Na+, K+, Mg2+…

Passive Transport of Ionic Drugs through Membranes with pH-Dependent Fixed Charges

2001

We have studied both theoretically and experimentally the passive transport of ionic drugs through membranes with pH-dependent fixed charge. The system considered constitutes a simplified model for pH-controlled drug delivery through membranes of biochemical and pharmaceutical interest. The theoretical approach employed is based on the Nernst-Planck flux equations and all of the species present in the system (the neutral or ionic drug and the hydrogen and hydroxide ions) have been taken into account together with a Langmuir-type isotherm for the adsorption of the ionic drug onto the membrane surface. The membrane permeabilities of cationic, anionic, and neutral drugs through porous membrane…

The Electrostatic Expansion of Linear Polyelectrolytes:  Effects of Gegenions, Co-ions, and Hydrophobicity

1997

The molar mass and ionic strength dependence of the dimensions of hydrophobically modified poly(vinylpyridinium) cations are demonstrated to be almost perfectly described by a theoretical expression derived on the basis of only excluded volume considerations. Generally, the effective charge density of the polyions decreases significantly with increasing hydrophobicity and with increasing polarizability of the gegenions. Unexpectedly, the intrinsic excluded volume effect which becomes dominating at high ionic strength not only depends on the hydrophobicity of the polyion but also significantly increases with decreasing polarizability of the gegenions (i.e., if the iodide gegenions are replac…

Micelles of polyisobutylene-block-poly(methacrylic acid) diblock copolymers and their water-soluble interpolyelectrolyte complexes formed with quater…

2004

The micellization of ionic amphiphilic diblock copolymers, polyisobutylene-block-poly(methacrylic acid) (PIB-b-PMAA), with a constant degree of polymerization of the non-ionic block ðDPn ¼ 20Þ and various degrees of polymerization of the polyelectrolyte block ðDPn ¼ 100 – 425Þ was examined in aqueous media by means of fluorescence spectroscopy using pyrene as a polarity probe. The molar values of the critical micellization concentration (cmc) were found to be around 2 £ 10 26 mol/l, being nearly independent of the length of the polyelectrolyte block as well as pH (in the range 6 – 9) and ionic strength (# 0.5 M NaCl) while the specific cmc values varied from 20 to 100 mg/l. Small-angle neut…

1990

It is shown that the block-like structure of the polyampholyte poly(methacrylic acid)-block-poly(1-methyl-4-vinylpyridinium chloride) considerably influences its conformational behaviour. This specific behaviour is explained by the formation of intra-macromolecular polyelectrolyte complexes stabilized by cooperative ionic contacts between acidic and basic units near the isoelectric point (i. e. p.). The structure of the block-polyampholyte at the i. e. p. is suggested to be close to the structure of non-stoichiometric polyelectrolyte complexes. The complex formation ability of the block-polyampholyte with respect to anionic, cationic, and nonionic polymers is also studied. By means of poten…

Hyperbranched polyethylenimines as versatile precursors for the preparation of different type of unimolecular micelles

2007

Abstract Hyperbranched polyethylenimine (HPEI) was successfully employed as precursor for the preparation of unimolecular inverted and aqueous micelles. The unimolecular inverted micelles (UIMs) obtained by the amidation of HPEI with 1,1′-carbonyldiimidazole (CDI) activated palmitic acid exhibited high encapsulation efficiency for hydrophilic anionic dyes and the efficiency could be enhanced significantly by decreasing the degree of amidation or quaternizing the residual amines. The weight ratio of loaded guests to the amidated HPEIs was not dependent on the molecular weight of HPEI core when the degree of amidation was kept constant. Decreasing the length of the aliphatic chain from 16 to …