Temperature-induced association and gelation of aqueous solutions of pectin. A dynamic light scattering study

Dynamic light scattering (DLS) measurements were carried out on aqueous solutions of low-methoxyl pectin at different temperatures and polymer concentration. Low temperature and increased polymer concentration promote the formation of multichain aggregates. The time correlation data obtained from the DLS experiments revealed, for all polymer solutions, the existence of two relaxation modes, one single exponential at short times followed by a stretched exponential at longer times. In the semidilute regime, a temperature reduction induced enhanced chain associations in the solutions with high values of the slow relaxation time and a strong wave vector dependence of the slow mode. These features could be rationalized in the framework of the coupling model of Ngai. At low temperatures (10 °C), gelation occurs in the semidilute regime and a transparent gel is formed. In this state, the profile of the correlation function changes and nonergodic signs are observed. The conjecture is that the association complexes and the gel network are stabilized through intermolecular hydrogen bonds, which are broken-up at higher temperatures. The hydrogen-bonded structures are formed in a process where the polymer chains have been “zipped” together in a cooperative manner.     

Viscosity of aqueous DNA solutions determined using dynamic light scattering

Viscosity is a key parameter for characterising the behaviour of liquids and their flow. It is, however, difficult to measure precisely, reproducibly and accurately for aqueous solutions on a micro-litre volume scale, which is what is usually needed for biological samples. We report the development of a new method for measuring dynamic viscosity by measuring dynamic light scattering (DLS) data for a range of particles of well-defined size. Most applications of DLS involve determining particle size for samples of known viscosity. We inverted the usual protocol and endeavoured to determine viscosity for samples of known particle size. Viscosity measurements for water and aqueous solutions of calf thymus DNA made using DLS were compared with those from a U-tube viscometer. The styrene particles, frequently used as particle size standards, gave unsatisfactory results for our DNA samples as did C-6 derivatized silica and positively charged amino polystyrene microspheres. However, negatively charged carboxylate polystyrene microspheres particles readily gave accurate viscosity measurements over a range of temperatures (0-100 °C). The sample volume required depends on the cuvette used to measure DLS, but can be performed with samples sizes ranging from 40 to 3000 μL. The sample can then be recovered for subsequent experiments. The DLS method is simple to perform at different temperatures and provides data of accuracy significantly above that of a U-tube viscometer. Our results also indicate a way forward to account accurately for solution viscosity in the normal applications of DLS to particle size determination by including the appropriate non-interacting particles as an internal standard.     

Dynamic light scattering study of cetyltrimethylammonium bromide aqueous solutions

Cetyltrimethylammonium bromide (CTAB) aqueous solutions are studied by dynamic light scattering method in a wide concentration range covering the first and second critical micelle concentrations (CMC₁ and CMC₂, respectively). Nonmonotonic and ambiguous behavior of diffusion coefficients D with an increase in concentrations above CMC1 is revealed. An increase in the D values in the first decade of CTAB concentration above CMC1 agrees with known published data for aqueous solutions of ionic surfactants. It is shown that an increase in the ionic strength of solution with the addition of KBr leads to a decrease in the positive slope of the dependence of diffusion coefficients on CTAB concentration up to zero at 0.05 M KBr. Two relaxation processes corresponding to large and small D values are simultaneously observed in micellar solutions, beginning with 0.03 M CTAB concentration. The data obtained are compared with published data, as well as with the results of viscosity measurements. The performed analysis indicates that the observed relaxation processes are explained by the coexistence of spherical and nonspherical micelles. It is established that micelles acquire a cylindrical shape at CTAB concentrations ranging from 0.2 to 0.25 M. Hydrodynamic radii and lengths of micelles are calculated.     

Study of aqueous solutions of fullerenol-d by the dynamic light scattering method

Dynamic light scattering method was used to determine the average size of fullerenol-d associates and the dependence of the electrokinetic ζ-potential on the concentration of aqueous solutions of fullerenol-d.     

Supramolecular structure of aqueous solutions of glucose according to dynamic light scattering data

The nature and structure of large-scale fluctuations in aqueous glucose solutions were studied by dynamic light scattering. The two-component model of solution was used. The supramolecular structure of the solutions was determined and their phase diagram at low concentrations was schematically constructed. The volume of clusters in solution was calculated.     

Characterization of riboflavin-photosensitized changes in aqueous solutions of alginate by dynamic light scattering

The effect of irradiation, in the wavelength range of 310-800 nm, on aqueous solutions (pH = 7.4) of alginate in the presence of the photosensitizer riboflavin (RF) has been investigated with the aid of dynamic light scattering (DLS). Under aerobic conditions light irradiation of RF causes scission of the polymer chains which affects the polymer dynamics. The time correlation data obtained from DLS experiments showed at all conditions the existence of two relaxation modes: one single exponential at short times, followed by a stretched exponential at longer times. The slow relaxation time revealed, over the whole considered concentration range, lower values for the alginate/RF system, whereas no effect of photochemical degradation was observed for the fast relaxation time in the semidilute regime. The results suggest that the photochemically induced fragmentation of alginate affects the slow relaxation mode, associated with disengagement relaxation of individual chains or cluster relaxation, in a similar way as the zero-shear viscosity. These findings provide detailed insight into the dynamics of the polymer matrix, and this knowledge can be useful in the context of controlled-release delivery of drugs. The chemical units of alginate (M = mannuronic acid and G = guluronic acid).     

Associative phase separation of beta-lactoglobulin/pectin solutions: a kinetic study by small angle static light scattering

Interpolymer complexation between beta-lactoglobulin (beta-lg) and pectin led to phase separation. Small angle static light scattering and phase contrast microscopy were used to monitor the phase separation of beta-lg/low-methoxyl or high-methoxyl-pectin (LM- or HM-pectin) dispersions as they were slowly acidified from pH 7 to 4 with glucono-delta-lactone (GDL). The monotonic decrease in scattered light intensity with the wave vector was associated with a nucleation and growth phase separation mechanism. Microscopic observations and turbidity measurements showed the increase of complex amounts with lower pH and at higher beta-lg/pectin ratios. The formation of intrapolymer complexes was initiated at pH 6.4 with the LM-pectin and at pH 5.0 with the HM-pectin. Local ordering with increasing amounts of small complexes was observed as scattered light intensity increased at intermediate q values. The beta-lg/LM-pectin complexes at the 5:1 and the 2:1 weight ratios and the beta-lg/HM-pectin complexes at 5:1 weight ratio have fractal structures. The formation of large amounts of small assemblies and sedimentation would be responsible for the decrease in the number and volume mean diameters and fractal dimension of beta-lg/LM-pectin complexes over time.     

Microfluidic light scattering as a tool to study the structure of aqueous polymer solutions

A small-angle light scattering (SALS) apparatus, coupled with a specially designed microfluidic device is shown to monitor the formation and subsequent size distribution of giant multilamellar vesicles of a diblock copolymer in aqueous solution. The closed-face design, fabricated between glass slides using a UV-curable optical adhesive, incorporates multiple inlets, a mixing system, and a viewing window to perform on-line SALS. The mixing of each component is tested using polystyrene latex microspheres. Vesicles of the block copolymer, EO6BO11 in aqueous solution are formed on the SALS chip and the pair distance distribution function determined using an inverse Fourier transformation of the scattered intensity to quantify the population and distribution for a range of vesicle sizes. These experiments provide demonstrations of how SALS on a microfluidic device can be used as a rapid screening tool to optimize processing conditions for a range of polymer solutions.     

Features of light scattering in aqueous solutions of dimethyl sulfoxide

The water-dimethyl sulfoxide (DMSO) system was studied by means of static light scattering in the concentration range of 0 to 60 mol % DMSO at 20 and 50°C. In the concentration range of 10 mol % DMSO, an abnormal maximum of scattered light was detected, the intensity of which decreases with an increase of temperature. The formation of this maximum is related to hydrophobic effects in the system under study and the existence of an unattainable critical point of delayering. Temperature inversion of light scattering intensity was detected at ∼14 mol % DMSO; at higher concentrations of DMSO, the intensity at 50°C is notably higher than at 20°C (due to the increase in the concentration’s degree of fluctuation upon an increase in temperature); at 60 mol % DMSO, intensities of scattered light at 20 and 50°C almost coincide. The apparent molar volumes of DMSO in solutions were calculated from the published data on density in the temperature range of 5 to 50°C. The minima of these values from 10 to 15 mol % DMSO (i.e., in the range of the abnormal maximum of scattered light) were obtained. The manifestation of hydrophobic effects in aqueous solutions of amphiphilic molecules is explained using the example of the DMSO-H₂O system.     

The solubilisation behaviour of some dichloroalkanes in aqueous solutions of PEO-PPO-PEO triblock copolymers: a dynamic light scattering, fluorescence spectroscopy, and SANS study

The aggregation behaviour of PEO-PPO-PEO triblock copolymers in water and in water + chlorinated additive mixtures was studied by means of fluorescence spectroscopy, dynamic light scattering (DLS), and small-angle neutron scattering (SANS). The copolymers were chosen such as to investigate the effects of molecular architecture (L35 and 10R5) and molecular weight by keeping constant the hydrophilic/hydrophobic balance (F88 and F108). 1,2-Dichloroethane was used as a prototype of water basins contaminants. The hydrodynamic radius of the block copolymer aggregates (R(h,M)) and the intensity ratio of pyrene of the first and the third vibrational band (I(1)/I(3)) were determined as a function of temperature (10-45 degrees C) and concentration. The copolymer architecture essentially does not affect R(h,M) in the entire range of temperature and concentration investigated. At a given temperature, increasing macromolecular size leads to a decrease of R(h,M). With rising temperature R(h,M) also decreases. According to the DLS results, the I(1)/I(3) change with temperature clearly detects the aggregation only for F88 and F108. The presence of 1,2-dichloroethane, at concentrations close to its solubility in water, does not lead to changes in the distribution of hydrodynamic radii for L35 and 10R5. Larger quantities of additive induce the formation of quite polydisperse mixed aggregates for L35 and of networks for 10R5. In the case of F88 and F108, low concentrations of additive lead to formation of mixed aggregates with smaller R(h,M). The SANS results corroborate the DLS and fluorescence findings proving enhancement of the copolymer aggregation through the presence of 1,2-dichloroethane. The DLS findings combined with those from the fluorescence spectroscopy provide some insight into the site of solubilisation of the additive in the aggregates.     

Inelastic light scattering measurements from linear polyelectrolyte aqueous salt solutions

Inelastic light scattering experiments demonstrate the existence of a conformational change upon ionization of a weak acid polyelectrolyte in aqueous salt solutions. The swelling of the polymeric coil occurs at a neutralization degree increasing with molecular weight.     

Polarized and depolarized dynamic light scattering of concentrated polystyrene solutions

Polarized and depolarized dynamic light scattering have been used to examine the dynamics of concentrated polystyrene solutions in dioctyl phthalate and toluene. Time-temperature superposition of the depolarized intensity correlation functions gave master curves covering more than 10 decades on the time scale. Polarized correlation functions are resolved into relaxational and diffusive components having different temperature dependences. When the relaxation rate of the concentration fluctuations approaches the reorientational relaxation rate, the concentration fluctuations become q-independent i.e. the diffusional relaxation is rate-determined by the backbone mobility. With a small molecule solvent as toluene, however, a part of the concentration fluctuations relaxes faster than the orientational relaxation, i.e., the diffusion occurs in the free volume within the “frozen” network.     

New class of aggregates in aqueous solution: an NMR, thermodynamic, and dynamic light scattering study

We investigated the aggregation properties of two classes of aromatic and hydrophobic compounds, namely chloroacetamides and ethyl 3-phenyl-2-nitropropionates, in moderately concentrated aqueous solution (millimolar range). The identification of all species present in solution under specific experimental conditions was performed by 1D and 2D NMR, pulsed gradient spin-echo NMR, and dynamic light scattering techniques. Some physical-chemical properties (viscosity, surface tension, and colligative properties) of the aqueous solutions were also determined. Both classes of compounds behave quite similarly: in solution, three distinct species, namely a monomeric species, small and mobile aggregates, and large and stiff aggregates, are observed. The results give insight into a new class of aggregates, held together by pi-pi interactions, which show an unusual associative behavior in water.     

Laser light scattering studies of poly(L-lysine HBr) in aqueous solutions

A simple theory for the relaxation of concentration fluctuations in polyelectrolyte solutions is presented, and particular results for the high-salt and no-salt limiting cases are discussed. Autocorrelation functions for the fluctuating intensity of scattered light from dilute aqueous solutions of poly(L -lysine HBr) (PLL-HBr) with and without added salt have been observed over a wide range of pH. The observed autocorrelation functions are in general very satisfactorily represented by single exponentials except at high pH (>10.5), where considerable aggregation is manifested. Solutions of PLL HBr without added salt exhibit extraordinary behavior, evident at low pH, involving a species with a very slowly decaying autocorrelation function. Though this species is readily annealed to a more ordinary individual free-molecule form by cycling the pH to 9.5 or higher and back, the resulting molecules are found to require unusually long times to reach internal configuration equilibrium under low pH conditions. Solutions of PLL-HBr in 0.2M NaBr and 0.1M NaCl are apparently free of similar extraordinary effects and show the normal isothermal helix–coil transition accompanied by a 15–30% rise in the diffusion coefficient to a maximum at pH 10.5, which is interpreted in terms of a change in molecular dimension of an interrupted helix. The predicted K² dependence of the reciprocal relaxation time and enhancement of the apparent diffusion coefficient of the polyelectrolyte in the absence of salt is confirmed.     

Dynamic light scattering from micelle complexes of cetyltrimethylammonium bromide-sodium salicylate in aqueous solutions

The diffusion coefficient of cetyltrimethylammonium bromide-sodium salicylate in aqueous solutions has been determined, using the dynamic light-scattering technique, as a function of sodium salicylate concentration, as well as of temperature. Using a gel model the results are discussed in terms of intermicellar pseudo-linkages, entanglements of threadlike micelles, and formation of pseudo-network.     

Nonmonotonic concentration dependences of elastic light scattering and its fluctuations in aqueous solutions

A nonmonotonic bimodal dependence of elastic, Rayleigh scattering on the potassium phenosan concentration in an aqueous solution has been revealed. A similar dependence has been found, for the first time, for scattering amplitude fluctuations. The observed correlation is indicative of structural transitions in hydration shells of potassium phenosan, which are responsible for the increase and scatter of their size comparable with the wavelength (527 nm) of a laser spectrometer.     

DNA condensation induced by cationic surfactant: a viscosimetry and dynamic light scattering study

The compaction of DNA induced by two simple amphiphiles, cetyltrimethylammonium bromide [CTAB] and dodecyldimethylamine oxide [DDAO], has been investigated by means of combined viscosity and dynamic light scattering measurements, to demonstrate the formation of soluble DNA/surfactant complexes, undergoing a coil-globule transition, upon the increase of the amphiphile concentration. In both of the two systems investigated, the complexation process reaches a maximum for a value of the surfactant to DNA phosphate groups molar ratio of about X = 1. Below this critical concentration, the coil and the globule state coexist in the solution, as clearly shown by the bimodal size distribution obtained from the light scattering intensity correlation functions. Some suggestions are given to support a molecular mechanism responsible for the complex formation, both in the case of a cationic surfactant (CTAB) and of a pH-dependent neutral or cationic amphiphile (DDAO), where the hydrophobic interactions play an important role.     

Effective interactions in lysozyme aqueous solutions: a small-angle neutron scattering and computer simulation study

We report protein-protein structure factors of aqueous lysozyme solutions at different pH and ionic strengths, as determined by small-angle neutron scattering experiments. The observed upturn of the structure factor at small wavevectors, as the pH increases, marks a crossover between two different regimes, one dominated by repulsive forces, and another one where attractive interactions become prominent, with the ensuing development of enhanced density fluctuations. In order to rationalize such experimental outcome from a microscopic viewpoint, we have carried out extensive simulations of different coarse-grained models. We have first studied a model in which macromolecules are described as soft spheres interacting through an attractive r(-6) potential, plus embedded pH-dependent discrete charges; we show that the uprise undergone by the structure factor is qualitatively predicted. We have then studied a Derjaguin-Landau-Verwey-Overbeek (DLVO) model, in which only central interactions are advocated; we demonstrate that this model leads to a protein-rich/protein-poor coexistence curve that agrees quite well with the experimental counterpart; experimental correlations are instead reproduced only at low pH and ionic strengths. We have finally investigated a third, "mixed" model in which the central attractive term of the DLVO potential is imported within the distributed-charge approach; it turns out that the different balance of interactions, with a much shorter-range attractive contribution, leads in this latter case to an improved agreement with the experimental crossover. We discuss the relationship between experimental correlations, phase coexistence, and features of effective interactions, as well as possible paths toward a quantitative prediction of structural properties of real lysozyme solutions.     

Association under shear flow in aqueous solutions of pectin

Effects of oscillatory and steady shear flows on intermolecular associations in dilute and semidilute aqueous solutions of pectin in the absence and presence of the hydrogen bond breaking agent urea are reported. A weak oscillatory shear perturbation builds up, depending on polymer concentration, multichain aggregates or networks in the course of time and these association structures are mainly stabilized through hydrogen bonds. The association effect is more pronounced at higher concentrations, and the growth of intermolecular interactions is inhibited by the addition of urea. Steady shear measurements on the pectin-water solutions reveal shear thickening at low shear rates for all the concentrations, except the lowest one, and disruption of intermolecular junctions at high shear rates. In the presence of urea, no shear thickening is detected. The polymer concentration dependence of the viscosity at a low shear rate can be described by a power law η ∼ c^x, with x = 1.9 and 1.4 without and with urea, respectively. When a low constant shear rate is applied to pectin solutions and this monitoring shear rate is interrupted periodically by transitory high shear rates perturbations during a short time, prominent association structures evolve upon return to the monitoring shear rate. This effect is more evident at a lower polymer concentration, and in the presence of urea, the growth of the association complexes is damped. The shear-induced alignment and stretching of polymer chains and the formation of hydrogen-bonded structures are analyzed in the framework of a model, where cooperative zipping of stretched chains play an important role. Viscosity enhancement is found for a semidilute pectin-water solution in the presence of moderate levels of salt addition (NaCl), suggesting that partial screening of electrostatic interactions promotes growth of energetic cross-links.     

Zinc-binding activity of different pectin compounds in aqueous solutions

The zinc-binding activity of different water-soluble pectin compounds varying according to their degree of esterification and of insoluble calcium pectate beads in aqueous solution was studied in a batch sorption system. The zinc uptake by all pectin compounds was highest within the pH range from 4.0 to 7.0. The binding capacities and rates of zinc ions by pectin compounds were evaluated. The Langmuir, Freundlich, and BET sorption models were applied to describe the isotherms and constants. Sorption isotherm data could be well interpreted by the Langmuir equation. The results obtained through the study suggest that pectin compounds are favorable sorbents. The largest number of zinc ions are bound by pectin with the degree of esterification close to zero. Therefore, it can be concluded that low-esterified pectins are more effective substances for elimination of zinc ions from aqueous disposals.