ترغب بنشر مسار تعليمي؟ اضغط هنا

Effect of electrolyte on the microstructure and yielding of aqueous dispersions of colloidal clay

69   0   0.0 ( 0 )
 نشر من قبل Samim Ali
 تاريخ النشر 2015
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Na-montmorillonite is a natural clay mineral and is available in abundance in nature. The aqueous dispersions of charged and anisotropic platelets of this mineral exhibit non-ergodic kinetically arrested states ranging from soft glassy phases dominated by interparticle repulsions to colloidal gels stabilized by salt induced attractive interactions. When the salt concentration in the dispersing medium is varied systematically, viscoelasticity and yield stress of the dispersion show non-monotonic behavior at a critical salt concentration, thus signifying a morphological change in the dispersion microstructures. We directly visualize the microscopic structures of these kinetically arrested phases using cryogenic scanning electron microscopy. We observe the existence of honeycomb-like network morphologies for a wide range of salt concentrations. The transition of the gel morphology, dominated by overlapping coin (OC) and house of cards (HoC) associations of clay particles at low salt concentrations to a new network structure dominated by face-face coagulation of platelets, is observed across the critical salt concentration. We further assess the stability of these gels under gravity using electroacoustics. This study, performed for concentrated clay dispersions for a wide concentration range of externally added salt, is useful in our understanding of many geophysical phenomena that involve the salt induced aggregation of natural clay minerals.

قيم البحث

اقرأ أيضاً

The rheological response, in particular the non-linear response, to oscillatory shear is experimentally investigated in colloidal glasses. The glasses are highly concentrated binary hard-sphere mixtures with relatively large size disparities. For a s ize ratio of 0.2, a strong reduction of the normalized elastic moduli, the yield strain and stress and, for some samples, even melting of the glass to a fluid is observed upon addition of the second species. This is attributed to the more efficient packing, as indicated by the shift of random close packing to larger total volume fractions. This leads to an increase in free volume which favours cage deformations and hence a loosening of the cage. Cage deformations are also favoured by the structural heterogeneity introduced by the second species. For a limited parameter range, we furthermore found indications of two-step yielding, as has been reported previously for attractive glasses. In samples containing spheres with more comparable sizes, namely a size ratio of 0.38, the cage seems less distorted and structural heterogeneities on larger length scales seem to become important. The limited structural changes are reflected in only a small reduction of the moduli, yield strain and stress.
Synthetic hectorite clay Laponite RD/XLG is composed of disk-shaped nanoparticles that acquire dissimilar charges when suspended in an aqueous media. Owing to their property to spontaneously self-assemble, Laponite is used as a rheology modifier in a variety of commercial water-based products. Particularly, aqueous dispersion of Laponite undergoes liquid - to - solid transition at about 1 volume % concentration. The evolution of the physical properties as dispersion transforms to solid state is reminiscent of physical aging in molecular as well as colloidal glasses. The corresponding soft glassy dynamics of an aqueous Laponite dispersion, including the rheological behavior, has been extensively studied in the literature. In this feature article we take an overview of recent advances in understanding soft glassy dynamics and various efforts taken to understand the peculiar rheological behaviors. Furthermore, the continuously developing microstructure that is responsible for eventual formation of soft solid state that supports its own weight against gravity has also been a topic of intense debate and discussion. Particularly extensive experimental and theoretical studies lead to two types of microstructures for this system: an attractive gel-like or repulsive glass like. We carefully examine and critically analyze the literature and propose a state diagram that suggests aqueous Laponite dispersion to be present in an attractive gel state.
Aqueous suspensions of Laponite with discotic particles are well-studied and find a wide range of applications in industry. A new direction of their implementation is polymer composites that can exhibit improved physical properties.We have studied th e aging of aqueous suspensions of Laponite and sodium polystyrene sulfonate (PSS-Na) and both their microscopic (small-angle X-ray scattering, SAXS) and macroscopic (small amplitude oscillatory shear (SAOS) rheometry) properties. The concentration of Laponite, $C_L$, was fixed at 2.5% wt and concentration of PSS-Na, $C_p$, was varied within 0-0.5% wt (0-24.2~mM). It is shown that the adding of PSS-Na significantly accelerates the aging.Nevertheless, the systems were stable against the sedimentation, and the flocculation didnt occur. Polyelectrolyte induced the appearance of large-scale fractal heterogeneities, which became more compact in the course of the aging. Polyelectrolyte induced the appearance of large-scale fractal heterogeneities, which became more compact in the course of the aging.
In directionally-dried colloidal dispersions regular bands can appear behind the drying front, inclined at $pm45^circ$ to the drying line. Although these features have been noted to share visual similarities to shear bands in metal, no physical mecha nism for their formation has ever been suggested, until very recently. Here, through microscopy of silica and polystyrene dispersions, dried in Hele-Shaw cells, we demonstrate that the bands are indeed associated with local shear strains. We further show how the bands form, that they scale with the thickness of the drying layer, and that they are eliminated by the addition of salt to the drying dispersions. Finally, we reveal the origins of these bands in the compressive forces associated with drying, and show how they affect the optical properties (birefringence) of colloidal films and coatings.
This work discusses the sedimentation stability and aging of aqueous suspension of Laponite in the presence of cetyltrimethylammonium bromide (CTAB). The concentration of Laponite was fixed at the constant level $C_l=2$ %wt, which corresponds to the threshold between equilibrium gel IG$_1$ and repulsive gel IG$_2$ phases. The concentration of CTAB $C_s$ was within 0-0.3 %wt. In the presence of CTAB the Laponite aqueous suspensions were unstable against sedimentation and they separated out into upper and bottom layers (U- and B-layers, respectively). The dynamic light scattering technique revealed that the addition of CTAB even at rather small concentration, $C_s=0.0164$ %wt ($0.03 CEC$), induced noticeable changes in the aging dynamics of U-layer, and it was explained by equilibration of CTAB molecules that were initially non-uniformly distributed between different Laponite particles. Accelerated stability analysis by means of analytical centrifugation with rotor speed ${omega}=500-4000$ rpm revealed three sedimentation regimes: continuous (I, $C_s<0.14$ %wt), zone-like (II, $0.14<C_s<0.2$ %wt) and gel-like (III, $C_s >0.2$ %wt). It was demonstrated that B-layer was soft in the zone-like regime. The increase of ${omega}$ resulted in its supplementary compressing and the collapse of soft sediment above certain critical centrifugal acceleration.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا