Large Ionic Strength Research Articles

Granular aqueous suspensions with controlled interparticular friction and adhesion.

We present a simple route to obtain large quantities of suspensions of non-Brownian particles with stimuli-responsive surface properties to study the relation between their flow and interparticle interactions. We perform an alkaline hydrolysis reaction on poly(methyl methacrylate) (PMMA) particles to obtain poly(sodium methacrylate) (PMAA-Na) particles. We characterize the quasi-static macroscopic frictional response of their aqueous suspensions using a rotating drum. The suspensions are frictionless when the particles are dispersed in pure water. We relate this state to the presence of electrosteric repulsion between the charged surfaces of the ionized PMAA-Na particles in water. Then we add monovalent and multivalent ions (Na+, Ca2+, La3+) and we observe that the suspensions become frictional whatever the valency. For divalent and trivalent ions, the quasi-static avalanche angle θc at large ionic strength is greater than that of frictional PMMA particles in water, suggesting the presence of adhesion. Finally, a decrease in the pH of the suspending solution leads to a transition between a frictionless plateau and a frictional one. We perform atomic force microscopy (AFM) to relate our macroscopic observations to the surface features of the particles. In particular, we show that the increase in friction in the presence of multivalent ions or under acidic conditions is driven by a nanoscopic phase separation and the bundling of polyelectrolyte chains at the surface of the particle. Our results highlight the importance of surface interactions in the rheology of granular suspensions. Our particles provide a simple, yet flexible platform to study frictional suspension flows.

Contact between water vapor and silicate surface causes abiotic formation of reactive oxygen species in an anoxic atmosphere

Spontaneous generation of reactive oxygen species (ROS) in aqueous microdroplets or at a water vapor-silicate interface is a new source of redox chemistry. However, such generation occurs with difficulty in liquid water having a large ionic strength. We report that ROS is spontaneously produced when water vapor contacts hydrogen-bonded hydroxyl groups on a silicate surface. The evolution of hydrogen-bonded species such as hydroxyl groups was investigated by using two-dimensional, time-resolved FT-IR spectroscopy. The participation of water vapor in ROS generation is confirmed by investigating the reaction of D2O vapor and hydroxyl groups on a silicate surface. We propose a reaction pathway for ROS generation based on the change of the hydrogen-bonding network and corresponding electron transfer onto the silicate surface in the water vapor-solid contact process. Our observations suggest that ROS production from water vapor-silicate contact electrification could have contributed to oxidation during the Archean Eon before the Great Oxidation Event.

Removal of impurities from bismuth pickling solution using solvent extraction with TBP

This work proposes an extraction process for thorough removal of various impurities in crude bismuth. In the process, crude bismuth was pickled with nitric acid, and then the bismuth in the filtrate was extracted into the organic phase by TBP. After scrubbing with a saturated NaNO3 solution, stripping was carried out by NaOH solution, and a rod-shaped α-Bi2O3 precipitate was obtained. Increasing the concentration of NO3− and TBP and the ratio of Vo/Va could greatly increase the extraction efficiency of bismuth or the separation factor of impurities. Bismuth is extracted in the form of Bi(NO3)3·TBP, and the results of quantum chemical calculations indicated that both intermolecular forces and chemical bonds exist between the Bi(NO3)3 and TBP molecules. Thermodynamic analysis based on the Debye-Hückel equation under large ionic strength conditions showed that the extraction reaction is exothermic and proceeds spontaneously. Under the optimized extraction conditions, the extraction efficiency, elution efficiency, and stripping efficiency of bismuth were 98.5%, 0.55%, and 96.2%, respectively. All of the impurity elements were thoroughly removed after extraction. In particular, the separation factor βBi/M of M = Te, As, Cu, and Sb, which are prone to codeposition with bismuth during electrodeposition, were 160, 183, 982, and 359, respectively. The purity of α-Bi2O3 obtained by this method was as high as 99.95%

Co-transport of ball‐milled biochar and Cd2+ in saturated porous media

The combination of ball milling technology and biochar materials provides new prospects for environmentally friendly and sustainable environmental pollution control technologies, but comes with opportunities and risks. In this study, column experiments were used to evaluate the environmental behavior of ball‑milled biochar (BMBC). The results of the column experiments showed that BMBC transport increased with a high flow velocity, large medium size, high pH, and low ionic strength. Owing to the strong adsorption of Cd2+ by BMBC, the presence of BMBC in the medium led to a decrease in effluent Cd2+. The presence of Cd2+ in the solution slightly inhibited the transport of BMBC. The transport of Cd2+ was facilitated by BMBC due to the high affinity. Therefore, attention should be paid to favorable conditions for BMBC transport. This study provides a perspective to assess the behavior of BMBC in the environment and whether its interaction with Cd2+ will introduce new environmental hazards.

The desalting/salting pathway: a route to form metastable aggregates with tuneable morphologies and lifetimes.

We investigate the formation/re-dissociation mechanisms of hybrid complexes made from negatively charged PAA2k coated γ-Fe2O3 nanoparticles (NP) and positively charged polycations (PDADMAC) in aqueous solution in the regime of very high ionic strength (I). When the building blocks are mixed at large ionic strength (1 M NH4Cl), the electrostatic interaction is screened and complexation does not occur. If the ionic strength is then lowered down to a targeted ionic strength Itarget, there is a critical threshold Ic = 0.62 M at which complexation occurs, that is independent of the charge ratio Z and the pathway used to reduce salinity (drop-by-drop mixing or fast mixing). If salt is added back up to 1 M, the transition is not reversible and persistent out-of-equilibrium aggregates are formed. The lifetimes of such aggregates depends on Itarget: the closer Itarget to Ic is, the more difficult it is to dissolve the aggregates. Such peculiar behavior is driven by the inner structure of the complexes that are formed after desalting. When Itarget is far below Ic, strong electrostatic interactions induce the formation of dense, compact and frozen aggregates. Such aggregates can only poorly reorganize further on with time, which makes their dissolution upon resalting almost reversible. Conversely, when Itarget is close to Ic more open aggregates are formed due to weaker electrostatic interactions upon desalting. The system can thus rearrange with time to lower its free energy and reach more stable out-of-equilibrium states which are very difficult to dissociate back upon resalting, even at very high ionic strength.

Surface and Interfacial Interactions in Dodecane/Brine Pickering Emulsions Stabilized by the Combination of Cellulose Nanocrystals and Emulsifiers.

Interfacial properties of cellulose nanocrystals (CNC) and surfactants were studied in high ionic strength (I) brines and correlated to the stability of dodecane/brine Pickering emulsions. Bis-(2-hydroxyethyl) cocoalkylamine (CAA), dodecyltrimethylammonium bromide (DTAB), and octyl-β-d-glucopyranoside (OGP) were adsorbed onto CNC in American Petroleum Institute (API) brine (I = 1.9 M) and synthetic seawater (SSW), with I = 0.65 M. Raman spectroscopy indicated that hydroxyl groups on the CNC surface interact with all three surfactants in high ionic strength media. Ionic interactions still play a role at the very large ionic strengths studied herein. Despite all surfactants adsorbing onto CNC, only the surface tension of CAA solutions in both brines was increased by the addition of 0.5 wt % CNC. The effect was much more prominent in API than in SSW. Contact angle measurements indicated that CAA increased the wettability of CNC by both brines in dodecane; DTAB, on the other hand, decreased wettability. Emulsion stability studies revealed that ionic strength, wettability, adsorption energy, and oil content strongly affect emulsion stability, more so than surfactant adsorption. In API, CNC aggregates alone stabilized the emulsions better compared to samples with additional emulsifiers; the same was true in SSW for oil contents below 50% v/v. For oil contents above 50% v/v in SSW, CAA was either detrimental or failed to improve emulsion stability. On the other hand, DTAB increased the stability of dodecane in SSW emulsions. Emulsions stable for over 21 months were prepared with oil contents of 75% v/v. The adsorption of CAA onto CNC limits the migration of both CNC and CAA to the dodecane/brine interface, while DTAB adsorption has the opposite effect.

Functional groups ionization effect on conformational properties of dendritic molecular brushes

Conformational properties of dendronized molecular brushes with ionized terminal groups in the dilute solution were studied by the Scheutjens-Fleer numerical self-consistent field method. Brushes with the same molecular mass and grafting density of dendrons but different generation number were compared. The ionic strength was varied within the conditions of the good (athermal) solvent. It was shown that the brush thickness increases with the ionic strength decrease as a result of the deformation of grafted dendrons. The induced persistence length, which characterizes the contribution of the grafted branches into the bending elasticity of the brush, behaves differently at large and small ionic strengths. At high salt concentration the brushes with more branched dendrons show smaller bending elasticity similar to their neutral analogs. At low ionic strengths the induced persistence length increases by an order and depends very weakly on the dendron architecture.

Biocompatible Stimuli-Responsive W/O/W Multiple Emulsions Prepared by One-Step Mixing with a Single Diblock Copolymer Emulsifier

Multiple water-in-oil-in-water (W/O/W) emulsions are promising materials in designing carriers of hydrophilic molecules or drug delivery systems, provided stability issues are solved and biocompatible chemicals can be used. In this work, we designed a biocompatible amphiphilic copolymer, poly(dimethylsiloxane)-b-poly(2-(dimethylamino)ethyl methacrylate) (PDMS-b-PDMAEMA), that can stabilize emulsions made with various biocompatible oils. The hydrophilic/hydrophobic properties of the copolymer can be adjusted using both pH and ionic strength stimuli. Consequently, the making of O/W (oil in water), W/O (water in oil), and W/O/W emulsions can be achieved by sweeping the pH and ionic strength. Of importance, W/O/W emulsions are formulated over a large pH and ionic strength domain in a one-step emulsification process via transitional phase inversion and are stable for several months. Cryo-TEM and interfacial tension studies show that the formation of these W/O/W emulsions is likely to be correlated to the interfacial film curvature and microemulsion morphology.

Modeling the effects of water content on TiO2 nanoparticles transport in porous media

The transport of manufactured titanium dioxide (TiO2, rutile) nanoparticles (NP) in porous media was investigated by metric scale column experiments under different water saturation and ionic strength (IS) conditions.The NP breakthrough curves showed that TiO2 NP retention on the interface between air and water (AWI) and the interface between the solid and the fluid (SWI) is insignificant for an IS equal to or smaller than 3mM KCl. For larger IS, the retention is depending on the water content and the fluid velocity. The experiments, conducted with an IS of 5mM KCl, showed a significantly higher retention of NP than that observed under saturated conditions and very similar experimental conditions.Water flow was simulated using the standard Richards equation. The hydrodynamic model parameters for unsaturated flow were estimated through independent drainage experiments. A new mathematical model was developed to describe TiO2 NP transport and retention on SWI and AWI. The model accounts for the variation of water content and water velocity as a function of depth and takes into account the presence of the AWI and its role as a NP collector. Comparisons with experimental data showed that the suggested modeled processes can be used to quantify the NPs retentions at the AWI and SWI. The suggested model can be used for both saturated and unsaturated conditions and for a rather large range of velocities.

Structural and multi-scale rheophysical investigation of diphasic magneto-sensitive materials based on biopolymers.

We present a structural and a multi-scale rheophysical investigation of magneto-sensitive materials based on biopolymers, namely aqueous solutions of sodium alginate incorporating magnetic maghemite nanoparticles, functionalized with adsorbed negative citrate ions. The large alginate ionic strength impacts the structure and the rheology of these nanocomposites in zero magnetic field. In given physico-chemical conditions, the system is fluid and homogeneous on macroscopic scales while it is diphasic on microscopic ones, containing micro-droplets coming from the demixion of the system. These micro-droplets are liquid and deformable under magnetic field. Their under-field elongation and their zero-field relaxation are directly observed by optical microscopy to determine their interfacial tension, their magnetic susceptibility and their internal viscosity. A structural analysis of the solutions of alginate chains and of the phase-separated mixtures of alginate and nanoparticles by Small Angle Scattering completes the local description of the system.

Designing small-molecule catalysts for CO2 capture

One method for CO2 capture is to dissolve CO2 in water to form carbonic acid. This reaction (CO2+H20→H2CO3(aq)) is remarkably slow but is catalyzed in biological systems by an enzyme called carbonic anhydrase (CA). The catalyzed reaction is diffusion limited and occurs at near neutral pH. The enzyme catalytic center is composed of a Zn(II) ion that is coordinated by 3 histidine residues and an axial water/hydroxyl group. A nucleophilic attack by the hydroxyl group on the CO2 molecule is the first step in the reaction mechanism. Cu(II), Hg(II), Cd(II), Ni(II), Co(II) and Mn(II) can bind the CA binding site and substitute the zinc ion; however, only Co(II) yields rates comparable to Zn(II). Unfortunately, an enzyme, such as carbonic anhydrase, is not amenable for industrial applications where a wide range of physico-chemical conditions exist. Enzymes are vulnerable to large pressures, high temperature, and high ionic strength. Efforts to isolate the key structural features responsible for catalysis led to the development of small-molecule mimetics of the CA catalytic site. These mimetics can, in turn, be used as catalyst for CO2 sequestration. Two of the fastest catalyst are the cyclic molecules: 1, 4, 7, 10-tetraazacyclododedacane and 1, 5, 9-triazacyclododedacane (both complexed with a Zn(II) ion). Nitrogen atoms in these cyclic molecules mimic the imidazole nitrogens of the CA active site. It is possible to examine the energetics of these compounds using transition state theory for the purposes of designing more efficient catalysts. Transition state theory predicts that the reaction rate constant is proportional to exp(−Ea/kT), where Ea denotes the activation energy, k the Boltzmann constant, and T the temperature of the reaction. The activation energy is the energetic cost of forming the reaction transition state from the reactants. Ab initio calculations can yield the activation energy, which can, in principle, be used as a design metric for more efficient catalysts. Using this approach, the difference in kinetic rate constant between the tetra- and tri-aza dodecane catalysts can be determined. Furthermore, the rates of the corresponding Co(II) catalysts were explored. Our data suggests this is a viable method for the design of inorganic small-molecule catalysts.

Preliminary kinetic characterization of a copper amine oxidase from rat liver mitochondria matrix

Kinetic measurements of a novel copper-dependent amine oxidase, purified from rat liver mitochondria matrix, were carried out using various substrates in a large pH (5.6-10.2) and ionic strength range (5-200 mM), in order to study the docking of substrates to the enzyme and, as a consequence, to verify the physicochemical characteristics of the active site. Relatively small changes of V(max) values (approx. 2.5-folds) over the substrates tested, suggest that the rate determining step of the catalysis is only slightly affected by amine chemical structure. In contrast, the strong change of K(M) and k(c)/K(M) values (approx. two orders of magnitude) indicates electrostatic control of the docking process, since the changes of K(M) and k(c)/K(M) values appear due to the presence of positively charged groups in the substrate molecules. These results suggest the presence in the enzyme active site of two negatively charged amino acid residues which seem to interact with positively charged groups of the substrate molecules. Analogies and differences with bovine serum amine oxidase are also described.

On the Domain of Applicability of Currently used Force Fields for the Calculation of the Activity of Alkali Ions at Physiological Ionic Strength

Alkali ions are present in virtually all biological processes. Their energetic properties have been so far predicted mostly by MD or MC calculations based on effective potentials derived for infinite diluted conditions (i.e. a single ion surrounding solely by water molecules) [1]. However, in physiological conditions, the concentration of K+ is sub-molar in the cytoplasm [2], and it may be by one, or even two, orders of magnitude larger near globular proteins or nucleic acids and in the active sites of of enzymes or channels [3-5]. The presence of a large ionic strength I is likely to limit the accuracy of the currently used potentials.Here we will discuss recent calculations of the activity coefficients for K+,Na+ ions at increasing I. Such coefficients have been obtained by calculating the excess chemical potentials from thermodynamics integration [6], with several commonly used biomolecular force fields. Preliminary results show that classical force fields generally overestimate the activity coefficients of ions.[1] M. Patra and M. Karttunen. J. Comput. Chem., 25:678-689, 2004.[2] F.M. Ashcroft. Ion Channels and Disease. Academic Press, 1999.[3] D. A. Doyle, J. M. Cabral, R. A. Pfuetzner, A. Kuo, J. M. Gulbis, S. L. Cohen, B. T. Chait, and R. MacKinnon. Science, 280:69-77, 1998[4] C. Domene, S. Vemparala, S. Furini, K. Sharp, and M. L. Klein. J. Am. Chem. Soc, 130:11, 2008.[5] P. Auffinger and Y. Hashem. Curr. Opin. Stru. Biol, 17:325-333, 2007.[6] M. Ferrrario, G. Ciccoti, E. Spohr, T. Cartailler, and P. Turq. J. Chem. Phys., 117:4947-4953, 2002

Ferredoxin:NADP+ Oxidoreductase Association with Phycocyanin Modulates Its Properties

In photosynthetic organisms, ferredoxin:NADP(+) oxidoreductase (FNR) is known to provide NADPH for CO(2) assimilation, but it also utilizes NADPH to provide reduced ferredoxin. The cyanobacterium Synechocystis sp. strain PCC6803 produces two FNR isoforms, a small one (FNR(S)) similar to the one found in plant plastids and a large one (FNR(L)) that is associated with the phycobilisome, a light-harvesting complex. Here we show that a mutant lacking FNR(L) exhibits a higher NADP(+)/NADPH ratio. We also purified to homogeneity a phycobilisome subcomplex comprising FNR(L,) named FNR(L)-PC. The enzymatic activities of FNR(L)-PC were compared with those of FNR(S). During NADPH oxidation, FNR(L)-PC exhibits a 30% decrease in the Michaelis constant K(m)((NADPH)), and a 70% increase in K(m)((ferredoxin)), which is in agreement with its predicted lower activity of ferredoxin reduction. During NADP(+) reduction, the FNR(L)-PC shows a 29/43% decrease in the rate of single electron transfer from reduced ferredoxin in the presence/absence of NADP(+). The increase in K(m)((ferredoxin)) and the rate decrease of single reduction are attributed to steric hindrance by the phycocyanin moiety of FNR(L)-PC. Both isoforms are capable of catalyzing the NADP(+) reduction under multiple turnover conditions. Furthermore, we obtained evidence that, under high ionic strength conditions, electron transfer from reduced ferredoxin is rate limiting during this process. The differences that we observe might not fully explain the in vivo properties of the Synechocystis mutants expressing only one of the isoforms. Therefore, we advocate that FNR localization and/or substrates availability are essential in vivo.

Modeling the Adsorption and Coagulation of Fulvic Acids on Colloids by Brownian Dynamics Simulations

Humic substances (HS) play an important role in the reactivity and transport of colloids in natural environments. In particular, the presence of fulvic acids (FA) in natural waters modifies the interactions between inorganic particles and biopolymers and makes difficult to predict their stability with regard to aggregation processes. In this study, Brownian dynamics (BD) modeling is applied to quantify the interactions between negatively charged FA and (i) a positively charged inorganic particle and (ii) a rigid neutral polysaccharide in aqueous solutions. Hematite and schizophyllan are respectively used as model colloids. Modeling the adsorption of FA at the hematite particle surface and on the polysaccharide is based on van der Waals attractive forces and electrostatic interactions. Possible applications of the model, however, are not restricted to this system and any interaction potential or colloidal particle can be considered. The competition between FA adsorption and FA homocoagulation in solution is studied as function of the solution ionic strength. Results show that, under the conditions used, the amount of adsorbed FA is largely controlled by the solution ionic strength. At low ionic strength the amount of adsorbed FA is limited by the electrostatic repulsion between FA at the colloid surfaces and FA monolayers are formed. By increasing the ionic strength the number of adsorbed FA is found to increase. At a sufficiently large ionic strength, however, FA coagulation in solution may strongly compete with FA adsorption at the hematite and polysaccharide surfaces. FA aggregates then adsorb at the colloid surfaces to form extended and porous structures. Results also suggest that FA adsorption and structure of the adsorbed layers are mainly driven by the complex interplay between electrostatic attractive and repulsive interactions.

Stability of titania nanoparticles in soil suspensions and transport in saturated homogeneous soil columns

The stability of TiO 2 nanoparticles in soil suspensions and their transport behavior through saturated homogeneous soil columns were studied. The results showed that TiO 2 could remain suspended in soil suspensions even after settling for 10 days. The suspended TiO 2 contents in soil suspensions after 24 h were positively correlated with the dissolved organic carbon and clay content of the soils, but were negatively correlated with ionic strength, pH and zeta potential. In soils containing soil particles of relatively large diameters and lower solution ionic strengths, a significant portion of the TiO 2 (18.8–83.0%) readily passed through the soils columns, while TiO 2 was significantly retained by soils with higher clay contents and salinity. TiO 2 aggregate sizes in the column outflow significantly increased after passing through the soil columns. The estimated transport distances of TiO 2 in some soils ranged from 41.3 to 370 cm, indicating potential environmental risk of TiO 2 nanoparticles to deep soil layers.

Novel 4-carboxyphenyl-grafted screen-printed electrode for trace Cu(II) determination

This paper reports the interest of 4-carboxyphenyl-grafted screen-printed electrodes (4-CP-SPEs) for trace Cu(II) measurement in water samples. These novel sensors were easily prepared via electrochemically reduction of the corresponding diazonium salt. Detection of Cu(II) was then achieved by immersing the grafted electrode into the sample solution for 10 min, followed by the electrochemical measurement of accumulated metallic ions. The efficiency of the Cu(II) adsorption at the grafted layer was clearly demonstrated. 4-CP-SPEs were able to detect and quantify Cu(II) as low as 5 × 10 −9 and 10 −8 M in a large ionic strength range. Moreover, no major interference of Pb(II) in the determination of Cu(II) is expected in natural water. Electrodes were finally successfully applied for Cu(II) determination in tap water and in estuarine water demonstrating the convenience of such sensors for environmental analysis.

Liquid-Liquid Interfacial Tension of Electrolyte Solutions

It is theoretically shown that the excess liquid-liquid interfacial tension between two electrolyte solutions as a function of the ionic strength I behaves asymptotically as O(-sqrt[I]) for small I and as O(+/-I) for large I. The former regime is dominated by the electrostatic potential due to an unequal partitioning of ions between the two liquids whereas the latter regime is related to a finite interfacial thickness. The crossover between the two asymptotic regimes depends sensitively on material parameters suggesting that the experimentally accessible range of ionic strengths can correspond to either the small or the large ionic strength regime. In the limiting case of a liquid-gas surface where ion partitioning is absent, the image charge interaction can dominate the surface tension for small ionic strength I such that an Onsager-Samaras limiting law O(-Iln(I)) is expected.

Aggregation and surface properties of F-specific RNA phages: Implication for membrane filtration processes

We report an experimental investigation of the electrokinetic properties and size variations of four F-specific bacteriophages of the types MS2, GA, Qβ and SP (21–30nm in diameter) over a broad range of pH values (1.5–7.5) and NaNO3 electrolyte concentrations (1–100mM). The results obtained by dynamic light scattering show that the aggregation of SP and GA particles takes place over the whole range of pH and ionic strength conditions examined. For MS2 phages, the aggregation of MS2 particles is not observed for pH higher than the isoelectric point (pI) and large ionic strengths for which interparticular repulsive electrostatic interactions are however expected to be sufficiently screened. Aggregation of the MS2 phages, dispersed in 1 and 100mM electrolyte concentration, occurs at pH 4, which basically corresponds to the pI as determined by electrophoresis measurements. The Qβ particles suspended in solutions of low electrolyte concentrations aggregate at low pH values (pI∼3) and, unlike MS2, at large ionic strengths over the whole range of pH conditions considered in this study. These elements allow the determination of the hydrophobic sequence for the four phages SP∼GA>Qβ>MS2. Close inspection of the electrokinetic results reveals small to significant variations of the pI values—depending on the phage considered—with respect to the concentration of indifferent NaNO3 electrolyte. This indicates that features other than chemical and electrostatic in nature play a key role in determining the pI and more generally the electrophoretic mobility μ of viral particles. A qualitative interpretation is given and is based on the consideration of inner electro-osmotic flow within the isolated or aggregated particles. The impact of the flow properties within the particles is further in agreement with recent theoretical formalism developed for the electrokinetics of soft multiplayer particles, the phages analyzed here being some illustrative examples. The determination and qualitative interpretation of the surface properties of the viral particles as reported in the current study are commented within the context of water treatment especially concerning viral removal by membrane filtration processes.

Relationship between Swelling and the Electrohydrodynamic Properties of Functionalized Carboxymethyldextran Macromolecules

The electrostatic, hydrodynamic, and swelling properties of a well-defined, functionalized carboxymethyldextran (CMD) polysaccharide are investigated in aqueous NaNO3 solution over a broad ionic strength range. The impact of the polycarboxylate charge and molar mass of the CMD macromolecules on their electrohydrodynamic features is thoroughly examined by combined protolytic titration, dynamic light scattering, and electrokinetic analyses. Electrophoretic mobility data obtained for sufficiently high electrolyte concentrations reveal a typical soft particle behavior. Upon decrease of the ionic strength, mobilities strongly increase in magnitude while significant electrostatic swelling takes place, as reflected in a decrease in the diffusion coefficients. CMD entities undergo conformational transitions from compact random coil at large ionic strengths to swollen coil and possibly a wormlike structure at lower NaNO3 concentrations. The magnitude of the variations in size and mobility with electrolyte concentration strongly depends on the overall charge of the CMD entity as well as on its molar mass. These factors control the stiffness of the constituent polymer chains and thus the degree of macromolecular permeability ("softness"). Using the soft-diffuse interface formalism previously developed for the electrohydrodynamics of charged permeable macromolecules, a quantitative analysis of the electrophoretic mobility data is presented. The measured values of the diffusion coefficient and space charge density Gamma degrees, as evaluated independently from the modeling of potentiometric titration curves, are taken into account in a self-consistent manner. It is found that large CMD entities of low charge densities are the most permeable to flow penetration with a limited heterogeneous electrostatic stiffening of the chains, whereas small CMD entities of larger Gamma degrees significantly expand upon lowering the ionic strength, giving rise to a strong anisotropy for the spatial distribution of polymer chain density.