Charge density parameter, cationic

Table 1. Ionic Radii, hydration numbers, softness parameters a, surface charge densities, polarizabilities, free energies AG° enthalpies AH° and entropies A S° of hydration of metal cations from groups Za o,nd II ...

The internal structure of the complexes can directly determine the mechanism of transfection [4, 23, 25]. We have found that for Lac CL-DNA complexes, the membrane charge density (aM) is a predictive parameter for transfection efficiency [21] (see Sect. 2), i.e., the data for monovalent and multivalent cationic lipids are described by a simple bell-curve. In contrast, for inverted hexagonal HnC CL-DNA complexes, TE is independent of aM, suggesting a distinctly different mechanism of transfection. Consistent with the TE data, confocal microscopy revealed distinctly different CL-DNA complex pathways and interactions with cells, which depended on both the structure (HnC vs Lac) and, for Lr/ complexes, on aM [25]. Thus, the mechanism of transfection by CL-DNA complexes is dependent both on their structure and, for a given structure, on chemical and physical parameters of the complexes. 

The present review deals mainly with two examples of polyelectrolyte phase behavior as discussed above. As an example for an H-type precipitation, the solution properties of polyvinylpyridinium chains are monitored as function of added inert salt. Here, we focus on the determination of the effective charge density and of the solvent quality parameter which are supposed to play a central role for the understanding of polyelectrolyte solution without specific counterion interactions. The second system under investigation comprises the interaction of polyacrylic acid with alkaline earth cations which exhibit very specific interactions, thus representing an example for type L-precipitation. Here the coil dimensions close to the phase boundary are compared to those close to type H-precipitation with inert added salt. 

Figure 5.39. Theoretical (a) and experimental (b) amount adsorbed as a function of the salt concentration for polyelectrolytes of varying charge density a, as Indicated. The theoretical figure was calculated for 0-6 and a surface charge density

Abstract Two types of membrane are presented free-standing films which are formed from aqueous polyelectrolyte solutions and membranes prepared by alternating electrostatic layer-by-layer assembly of cationic and anionic polyelectrolytes on porous supports. Layer-by-layer assemblies represent versatile membranes suitable for dehydration of organic solvents and ion separation in aqueous solution. The results show that the structuring of the polyelectrolytes in the liquid films and the permeability of the multilayer membranes depends on different internal and environmental parameters, for example molecular weight, polymer charge density, ionic strength, and temperature. 

The chemistry of natural zeolites may have important effects on their ion exchange properties, mainly in terms of selectivity. It is well known that selectivity is a function of various parameters, depending on (1) framework topology, (2) ion size and shape, (3) charge density on the anionic framework, (4) ion valence and (5) electrolyte concentration in the aqueous phase [51]. Within the same zeolite type, the variation of the framework composition (in practice, Si/Al ratio) and therefore of the framework charge density, affects the cation selectivity [52], as it has experimentally been proven for phillipsitc [53]. It is improper, stricto sensu, to compare with each other, in terms of selectivity behaviour, different zeolites having... 

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