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Yogesh M Joshi

Publications and source records attributed to Yogesh M Joshi.

At least 19 recordsLinked to original sources

Analysing gelation transition through fractional viscoelasticity and Mittag-Leffler-Prabhakar function

The gelation transition, a process that transforms a flowable liquid into an elastic solid, occurs in a variety of systems, ranging from colloidal to polymeric. During the gelation transition, a system passes through a critical gel state characterized by scale-free power-law viscoelasticity. Interestingly, the fractional calculus provides a natural mathematical language for such power-law viscoelasticity. In this work, we develop physically constrained fractional viscoelastic models, as well as those based on the three-parameter Mittag-Leffler-Prabhakar function, for both the pre-gel and post-gel regimes, ensuring consistency with the conventional scaling relations in each regime. While the fractional pre-gel model is observed to be valid only for a restricted subset of parameter values, the Prabhakar function-based model for relaxation modulus, which translates into Havriliak-Negami function based complex modulus, rigorously removes this limitation while simultaneously providing profound molecular significance. We enforce continuity of the dynamic moduli and their derivatives across the critical gel point, which universally imposes a symmetry in the relaxation dynamics on either side of the critical gel state. Such enforcement further validates the hyper-scaling relation connecting the critical exponents, making it a theoretical necessity rather than an empirical coincidence. We validate the proposed models against time- and frequency-domain experimental data. A model-agnostic, frequency-independent rheological fingerprint of the critical gel state, uniquely determined by two critical exponents, is also identified.

cond-mat.soft

Evolution of Linear Viscoelasticity across the Critical Gelation Transition

In this work, we develop a rigorous theoretical framework for the evolution of linear viscoelastic properties across the sol-gel transition. More specifically, we derive general admissible expressions for the relaxation modulus and dynamic moduli as the critical gel state is approached from the pre-gel or the post-gel side. These expressions possess a generalized multi-mode series representation and recover the critical gel power law spectrum in the limit of vanishing distance from the gel point. We validate these expressions against the experimental data for various polymeric and colloidal systems. A central finding of the present work is the requirement of continuity of the dynamic moduli and their derivatives at the critical gel point, which imposes a profound physical constraint, necessitating the relaxation dynamics on both sides of the transition to be symmetric. This, in turn, leads to the hyper-scaling relation, which is a theoretical requirement rather than an empirical proposal. We further show that the critical relaxation exponent (n) always remains above the relaxation scaling exponent (κ), establishing a previously unrecognized lower bound on n. We also analytically estimate, for the first time, the parameter C that characterizes the relative evolution of the storage modulus with respect to the loss modulus as the critical state is approached. These results reveal that the symmetry, scaling, and hyperscaling properties of the sol-gel transition are all consequences of a single unifying physical requirement originating from the continuity of the linear viscoelastic properties at the critical gel point.

cond-mat.soft

Thermal History Asymmetry and Dissipation in Dense Colloidal Microgel Glasses

Microstructurally arrested matter, from molecular glasses to soft glassy materials, can retain a memory of their thermal or mechanical (shear) histories. Their history-dependent and nonlinear microstructural recoveries have been studied within the Kovacs framework. Here, we applied the temperature ramps of varying magnitudes to dense colloidal suspensions of thermoresponsive, deformable and compressible microgel particles should serve as an effective strategy to probe the nonlinear path-dependent structural recovery of these systems. We synthesised Poly (N-isopropyl acrylamide) (PNIPAM) microgel particles using the free radical precipitation polymerisation method. Using oscillatory rheology, we studied the relaxations of the viscoelastic moduli of dense PNIPAM suspensions that were heated and cooled at various temperature ramp rates. Path-dependent structural recovery was quantified by studying the asymmetric approach of the suspension elastic modulus toward the target temperature during the heating and cooling temperature ramps. The loss modulus peaks, observed at the times of initiation and termination of the temperature ramps, were understood to arise from energy dissipation due to microgel rearrangement events. The heights of the peaks were found to be inversely correlated with the asymmetry in the elastic response. Our work highlights the important role of energy dissipation through microgel rearrangements in eliminating path-dependent asymmetries in the storage moduli of dense PNIPAM suspensions subjected to thermal shocks. By tuning the applied temperature ramp rate and particle packing density, therefore, asymmetric storage modulus relaxations in dense systems can be modulated via adjustments of the accessible free volume.

cond-mat.soft

Shear Stress Build-up Under Constant Strain Conditions in Soft Glassy Materials

In this work, we investigate the transient rheological behavior of two soft glassy materials: a clay dispersion and a silica gel, emphasizing their unconventional shear stress build-up behavior under conditions of constant imposed strain. For both materials, the elastic modulus and static yield stress undergo time-dependent evolution or aging. In addition, following an intense period of pre-shearing (i.e. shear-melting or destructuration), the material relaxation time is observed to show a stronger than linear dependence on the sample age, suggestive of hyper-aging dynamics. We show that these features are consistent with non-monotonic steady-state shear stress/shear rate flow curves characterized by a local stress minimum. When a steady shear flow is suddenly ceased, and the total imposed sample strain is held constant, both materials show an initial relaxation of the shear stress followed by a period of shear stress buildup, resulting in a local minimum in the evolution of shear stress with time. For the clay dispersion, the intensity of these effects increases with higher pre-shear rates, whereas for the silica gel, the effects are largely independent of the pre-shear rate. We also propose a simple time-dependent linear Maxwell model, which qualitatively predicts the experimentally observed trends in which the shear stress build-up is directly related to a monotonic increase in the elastic modulus, giving keen insight into this peculiar phenomenon.

cond-mat.soft

Aqueous Laponite Dispersions are Attractive Gels, Not Repulsive Wigner Glasses: A Critical Commentary

An aqueous dispersion of Laponite has been studied in the literature for over the past three decades. Typically, the aqueous dispersion of Laponite undergoes incessant evolution of its microstructure, wherein its elastic modulus and the mean relaxation time show a continuous increase as a function of time. A considerable amount of discussion has revolved around the nature of this dispersion, specifically whether it can be classified as a repulsive Wigner glass state, characterized by disconnected Laponite particles stabilized by electrostatic repulsions, or an attractive gel state, in which the particles form a percolated space-spanning network. The proponents of the Wigner glass state also conjecture that this system experiences a glass-glass transition after a period of two days has elapsed since its preparation. In this commentary, we explore this topic from a rheological point of view analyzing the published literature and performing new experiments. Aided by additional evidence from the literature, we propose that rheological behavior overwhelmingly suggests that an aqueous dispersion of Laponite undergoes sol - attractive gel transition and remains in the attractive gel state over at least up to 7 days without undergoing any additional transition. Importantly, rheology, despite being a macroscopic tool governed by principles of mechanics, offers profound insight into the microstructure of this particular system. The corresponding analysis conclusively determines the state of an aqueous dispersion of Laponite to be an attractive gel.

cond-mat.soft

Exploring Thixotropic Timescale: Phenomenological Insights and Analytical Perspectives

Thixotropy is characterized by an increase in viscosity when a material is subjected to no flow (quiescent) or weak flow conditions and a decrease in viscosity when it is subjected to strong flow conditions. The characteristic timescale associated with the thixotropic phenomenon, particularly how the viscosity increases with time, has been termed the thixotropic timescale. In the literature, several approaches have been suggested for estimating the thixotropic timescale. The most prominent approach, however, infers it from a specific form of a kinetic expression for structure parameter evolution. In this paper, we study the various kinds of structural kinetic models, and by carrying out a careful analysis of the same, we propose a parameter for the thixotropic timescale that is associated with the most generic form of the kinetic expression for structure parameter evolution. We observe that when the viscosity of the structural kinetic model undergoes continuous increase with time and eventually diverges under quiescent conditions, which we believe is the most practical scenario, our analysis suggests that increasing the thixotropic timescale weakens the thixotropic character of a system. We also propose a new phenomenological measure of the thixotropic timescale: ${{τ}_{thix}}={{\left( d\text{ln}η/dt \right)}^{-1}}$, where $η$ is viscosity and $t$ is time. The proposed definition allows a straightforward and unique way to determine thixotropic timescale through experiments and agrees well with the conventional notion of thixotropy.

cond-mat.soft

Effect of Thermal and Mechanical Rejuvenation on Rheological Behavior of Chocolate

Chocolate is known to undergo solid-liquid transition upon an increase in temperature as well as under application of deformation field. Upon sudden reduction in temperature from a molten state (or thermal rejuvenation), rheological properties of chocolate undergo evolution as a function of time under isothermal conditions, a behavior reminiscent of physical aging in polymeric glasses. Then again, subsequent to cessation of shear flow (or mechanical rejuvenation), chocolate shows temporal evolution of the rheological properties, a behavior similar to physical aging in soft glassy materials. In this work, we evaluate three rheological properties, namely, dynamic moduli, relaxation time spectrum and characteristic relaxation time of chocolate, and compare their evolution after thermal as well as mechanical rejuvenation. We observe that the evolution of the rheological properties subsequent to mechanical rejuvenation is distinctly different from that of thermal rejuvenation, wherein the evolution is more gradual in the former case. On the one hand, this work provides unique insights into how shear affects the rheological behavior of chocolate. On the other hand, this work clearly suggests that chocolate explores different sections of the energy landscape after mechanical rejuvenation compared to that of thermal rejuvenation.

cond-mat.soft

Thixotropy, non-monotonic stress relaxation, and the second law of thermodynamics

Many thixo-viscoelastic materials have been reported to undergo enhancement in elastic modulus with time and decrease in the same under application of deformation field. Incorporation of this feature in a viscoelastic structural kinetic model has an apparent possibility of violating the second law of thermodynamics. Furthermore, in a related experimental observation, stress has been reported to undergo a non-monotonic change as a function of time under the application of constant strain. We analyze both these scenarios through a structural kinetic model that shows viscoelastic aging but undergoes rejuvenation only due to the viscous rate of strain. We observe that such formalism does not violate the second law. Interestingly, the proposed simple formalism predicts the experimental observation of the non-monotonic stress relaxation very well.

cond-mat.soft

Effect of sodium pyrophosphate and understanding microstructure of aqueous LAPONITE(R) dispersion using dissolution study

We investigate physical origin of ergodicity breaking in an aqueous colloidal dispersion of synthetic hectorite clay, LAPONITE(R), by performing dissolution and rheological experiments with monovalent salt and tetrasodium pyrophosphate solution. We also study the effect of interface, nitrogen and paraffin oil on the same. Dissolution experiments carried out for dispersions with both the interfaces show similar results. However, for samples with nitrogen interface, all the effects are observed to get expedited in time compared to paraffin oil interface. When kept in contact with water, 1.5 wt. % and 2.8 wt. % colloidal dispersion at pH 10 swell at small ages, while do not swell at large ages. The solution of tetrasodium pyrophosphate, interestingly, dissolves the entire colloidal dispersion samples with pH 10 irrespective of the clay concentration. Experiments carried out on colloidal dispersions prepared in water having pH 13 demonstrate no effect of water as well as sodium pyrophosphate solution on the same suggesting a possibility of the presence of negative charge on edge at that pH. We believe that all the behaviors observed for samples at pH 10 can be explained by an attractive gel microstructure formed by edge-to-face contact. Furthermore, the absence of swelling in old colloidal dispersion at pH 10 and dissolution of the same by sodium pyrophosphate solution cannot be explained by merely repulsive interactions. This behavior suggests that attractive interactions play an important role in causing ergodicity breaking in the colloidal dispersions at pH 10 at all the ages irrespective of the clay concentration. We substantiate the presence of fractal network structure formed by interparticle edge-face association using rheological tools and cryo-TEM imaging. We also conduct a comprehensive study of the effect of sodium pyrophosphate in the sol-gel transition of LAPONITE(R) dispersion.

cond-mat.mtrl-sci

Phase Behavior of Aqueous Suspension of Laponite: New Insights with Microscopic Evidence

Investigating microstructure of suspensions with particles having anisotropic shape that share complex interactions is a challenging task leading to competing claims. This work investigates phase behavior of one such system: aqueous Laponite suspension, which is highly contested in the literature, using rheological and microscopic tools. Remarkably, we observe that over a broad range of Laponite (1.4 to 4 weight %) and salt concentrations (0 to 7 mM), the system overwhelmingly demonstrates all the rheological characteristics of the sol-gel transition leading to a percolated network. Analysis of the rheological response leads to fractal dimension that primarily depends on the Laponite concentration. We also obtain the activation energy for gelation, which is observed to decrease with increase in Laponite as well as salt concentration. Significantly, the cryo-TEM images of the post-gel state clearly show presence of a percolated network formed by inter-particle bonds. The present work therefore conclusively establishes the system to be in an attractive gel state resolving a long-standing debate in the literature.

cond-mat.soft

Characteristics of the secondary relaxation process in soft colloidal suspensions

A universal secondary relaxation process, known as the Johari-Goldstein (JG) $β$-relaxation process, appears in glass formers. It involves all parts of the molecule and is particularly important in glassy systems because of its very close relationship with the $α$-relaxation process. However, the absence of a J-G $β$-relaxation mode in colloidal glasses raises questions regarding its universality. In the present work, we study the microscopic relaxation processes in Laponite suspensions, a model soft glassy material, by dynamic light scattering (DLS) experiments. $α$ and $β$-relaxation timescales are estimated from the autocorrelation functions obtained by DLS measurements for Laponite suspensions with different concentrations, salt concentrations and temperatures. Our experimental results suggest that the $β$-relaxation process in Laponite suspensions involves all parts of the constituent Laponite particle. The ergodicity breaking time is also seen to be correlated with the characteristic time of the $β$-relaxation process for all Laponite concentrations, salt concentrations and temperatures. The width of the primary relaxation process is observed to be correlated with the secondary relaxation time. The secondary relaxation time is also very sensitive to the concentration of Laponite. We measure primitive relaxation timescales from the $α$-relaxation time and the stretching exponent ($β$) by applying the coupling model for highly correlated systems. The order of magnitude of the primitive relaxation time is very close to the secondary relaxation time. These observations indicate the presence of a J-G $β$-relaxation mode for soft colloidal suspensions of Laponite.

cond-mat.soft

Long Time Response of Aging Glassy Polymers

Aging amorphous polymeric materials undergo free volume relaxation, which causes slowing down of the relaxation dynamics as a function of time. The resulting time dependency poses difficulties in predicting their long time physical behavior. In this work, we apply effective time domain approach to the experimental data on aging amorphous polymers and demonstrate that it enables prediction of long time behavior over the extraordinary time scales. We demonstrate that, unlike the conventional methods, the proposed effective time domain approach can account for physical aging that occurs over the duration of the experiments. Furthermore, this procedure successfully describes time temperature superposition and time stress superposition. It can also allow incorporation of varying dependences of relaxation time on aging time as well as complicated but known deformation history in the same experiments. This work strongly suggests that the effective time domain approach can act as an important tool to analyze the long time physical behavior of aging amorphous polymeric materials. Aging amorphous polymeric materials undergo free volume relaxation, which causes slowing down of the relaxation dynamics as a function of time. The resulting time dependency poses difficulties in predicting their long time physical behavior. In this work, we apply effective time domain approach to the experimental data on aging amorphous polymers and demonstrate that it enables prediction of long time behavior over the extraordinary time scales. We demonstrate that, unlike the conventional methods, the proposed effective time domain approach can account for physical aging that occurs over the duration of the experiments. Furthermore, this procedure successfully describes time temperature superposition and time stress superposition.

cond-mat.mtrl-sci

Chemical Stability of Laponite in Aqueous Media

In this work stability of Laponite against dissolution in its aqueous dispersions is investigated as a function of initial pH of water before mixing Laponite, and concentration of Laponite. Dissolution of Laponite is quantified in terms of concentration of leached magnesium in the dispersions. Interestingly the solvent pH is observed to play no role in dissolution of Laponite in dispersion over the explored range of 3 to 10. Furthermore, contrary to the usual belief that Laponite dissolves when pH of aqueous dispersion decreases below 9, dissolution of the same is observed even though dispersion pH is above 10 for low concentrations of Laponite (1 and 1.7 mass%). On the other hand, for dispersions having high concentration of Laponite (2.8 mass%) and pH in the similar range (>10) no dissolution is observed. Measurement of ionic conductivity of dispersion shows that concentration of sodium ions in dispersion increases with concentration of Laponite, which appears to have a role in preventing the dissolution of Laponite.

cond-mat.mtrl-sci

Rheological Signatures of Gelation and Effect of Shear Melting on Aging Colloidal Suspension

Colloidal suspensions that are out of thermodynamic equilibrium undergo physical aging wherein their structure evolves to lower the free energy. In aqueous suspension of Laponite, physical aging accompanies increases of elastic and viscous moduli as a function of time. In this work we study temporal evolution of elastic and viscous moduli at different frequencies and observe that freshly prepared aqueous suspension of Laponite demonstrates identical rheological behavior reported for the crosslinking polymeric materials undergoing chemical gelation. Consequently at a certain time tanδ is observed to be independent of frequency. However, for samples preserved under rest condition for longer duration before applying the shear melting, the liquid to solid transition subsequent to shear melting shows greater deviation from classical gelation. We also obtain continuous relaxation time spectra from the frequency dependence of viscous modulus. We observe that, with increase in the rest time, continuous relaxation time spectrum shows gradual variation from negative slope, describing dominance of fast relaxation modes to positive slope representing dominance of slow relaxation modes. We propose that the deviation from gelation behavior for the shear melted suspensions originates from inability of shear melting to completely break the percolated structure thereby creating unbroken aggregates. The volume fraction of such unbroken aggregates increases with the rest time. For small rest times presence of fewer number of unbroken aggregates cause deviation from the classical gelation. On the other hand, at high rest times presence of greater fraction of unbroken aggregates subsequent to shear melting demonstrate dynamic arrest leading to inversion of relaxation time spectra.

cond-mat.soft

Thermal Diffusivity and Viscosity of Suspensions of Disc Shaped Nanoparticles

In this work we conduct a transient heat conduction experiment with an aqueous suspension of nanoparticle disks of Laponite JS, a sol forming grade, using laser light interferometry. The image sequence in time is used to measure thermal diffusivity and thermal conductivity of the suspension. Imaging of the temperature distribution is facilitated by the dependence of refractive index of the suspension on temperature itself. We observe that with the addition of 4 volume % of nano-disks in water, thermal conductivity of the suspension increases by around 30%. A theoretical model for thermal conductivity of the suspension of anisotropic particles by Fricke as well as by Hamilton and Crosser explains the trend of data well. In turn, it estimates thermal conductivity of the Laponite nanoparticle itself, which is otherwise difficult to measure in a direct manner. We also measure viscosity of the nanoparticle suspension using a concentric cylinder rheometer. Measurements are seen to follow quite well, the theoretical relation for viscosity of suspensions of oblate particles that includes up to two particle interaction. This result rules out the presence of clusters of particles in the suspension. The effective viscosity and thermal diffusivity data show that the shape of the particle has a role in determining enhancement of thermophysical properties of the suspension.

cond-mat.mes-hall

Physicochemical Effects in Aging Aqueous Laponite Suspensions

We study aging behavior of aqueous suspension of Laponite as a function of concentration of Laponite, concentration of salt, time elapsed since preparation of suspension (idle time) and temperature by carrying extensive rheological and conductivity experiments. We observe that temporal evolution of elastic modulus, which describes structural buildup and aging, shifts to low times for experiments carried out for higher concentration of Laponite, higher concentration of salt, greater temperature and on higher idle time while preserving the curvature of evolution in the solid regime. Consequently appropriate shifting of evolution of elastic modulus in the solid regime leads to aging time idle time salt concentration Laponite concentration temperature superposition. Existence of such superposition suggests generic nature of microstructure buildup irrespective of mentioned variables in the explored range. Behavior of shift factors needed to obtain the superposition indicate that energy barrier associated with structural buildup decreases with increase in idle time and temperature; and decreases linearly with increase in concentration of Laponite and that of salt. The conductivity experiments show that ionic conductivity of the suspension increases with increasing Laponite concentration, salt concentration, temperature and very importantly the idle time. We also analyze the interparticle interactions using DLVO theory that suggests increase in idle time, temperature and salt concentration increases height of repulsive energy barrier while decreases width of the same when particles approach each other in a parallel fashion. Analysis of rheological and conductivity experiments suggest strong influence of attractive interactions on the low energy structures in aqueous suspension of Laponite.

cond-mat.soft

Thermally Activated Asymmetric Structural Recovery in a Soft Glassy Nano-Clay Suspension

In this work we study structural recovery of a soft glassy Laponite suspension by monitoring temporal evolution of elastic modulus under isothermal conditions as well as following step temperature jumps. Interestingly, evolution behavior under isothermal conditions indicates the rate, and not the path of structural recovery, to be dependent on temperature. The experiments carried out under temperature jump conditions however trace a different path of structural recovery, which shows strong dependence on temperature and the direction of change. Further investigation of the system suggests that this behavior can be attributed to restricted mobility of counterions associated with Laponite particle at the time of temperature change, which do not allow counterion concentration to reach equilibrium value associated with the changed temperature. Interestingly this effect is observed to be comparable with other glassy molecular and soft materials, which while evolve in a self-similar fashion under isothermal conditions, show asymmetric behavior upon temperature change.

cond-mat.soft

Enhanced Thermal Transport through Soft Glassy Nano-disc Paste

We study diffusion of heat in an aqueous suspension of disc shaped nanoparticles of Laponite, which has finite elasticity and paste-like consistency, by using the Mach-Zehnder interferometer. We estimate the thermal diffusivity of the suspension by comparing the experimentally obtained temperature distribution to that with analytical solution. We observe that despite highly constrained Brownian diffusivity of particles owing to its soft glassy nature, suspensions at very small concentrations of Laponite demonstrates significant enhancement in thermal diffusivity. We correlate the observed enhancement with the possible microstructures of the Laponite suspension.

cond-mat.soft