Colloidal suspensions under external control

In this thesis, we developed ideas to control the structure and the dynamics\ud of colloidal suspensions by manipulating the boundary conditions\ud and applying external elds. The aforementioned manipulations\ud of colloidal \ud uids not only provide opportunities to improve\ud our understanding of fundamental physical phenomena, but also initiate\ud ideas for developing advanced materials. External control over\ud colloidal suspensions with hard-sphere like interactions -arguably the\ud simplest model system for soft matter studies- can be evoked to tune\ud the interplay between structure and dynamics for both equilibrium\ud and out-of-equilibrium systems. Interplay between structure and dynamics\ud is commonly encountered in Soft Matter systems including\ud but not limited to colloidal suspensions, emulsions, polymers, polyelectrolydes\ud and proteins

Industrial Separation Processes:Fundamentals

Separation processes on an industrial scale account for well over half of the capital and operating costs in the chemical industry. Knowledge of these processes is key for every student of chemical or process engineering. This book is ideally suited to university teaching, thanks to its wealth of exercises and solutions. The second edition boasts an even greater number of applied examples and case studies as well as references for further reading. - An authoritative introduction to industrial separation technology. - Contains exercises at the end of each subject as well as solutions. - Now with extended and updated examples and case studies

Calculating the motion of highly confined, arbitrary-shaped particles in Hele-Shaw channels

We combine theory, numerical calculations, and experiments to accurately predict the motion of anisotropic particles in shallow microfluidic channels, in which the particles are strongly confined in the vertical direction. We formulate an effective quasi-two-dimensional description of the Stokes flow around the particle via the Brinkman equation, which can be solved in a time that is two orders of magnitude faster than the three-dimensional problem. The computational speedup enables us to calculate the full trajectories of particles in the channel. To test our scheme, we study the motion of dumbbell-shaped particles that are produced in a microfluidic channel using `continuous flow lithography'. Contrary to what was reported in earlier work (Uspal et al., Nature communications 4 (2013)), we find that the reorientation time of a dumbbell particle in an external flow exhibits a minimum as a function of its disk size ratio. This finding is in excellent agreement with new experiments, thus confirming the predictive power of our scheme.Comment: 18 pages, 5 figures, 4 supplemental movie

Controlling and predicting droplet size of nanoemulsions: scaling relations with experimental validation

Gupta, Ankur et al. “Controlling and Predicting Droplet Size of Nanoemulsions: Scaling Relations with Experimental Validation.” Soft Matter 12.5 (2016): 1452–1458.Eni S.p.A

Nanoemulsions: formation, properties and applications

Nanoemulsions are kinetically stable liquid-in-liquid dispersions with droplet sizes on the order of 100 nm. Their small size leads to useful properties such as high surface area per unit volume, robust stability, optically transparent appearance, and tunable rheology. Nanoemulsions are finding application in diverse areas such as drug delivery, food, cosmetics, pharmaceuticals, and material synthesis. Additionally, they serve as model systems to understand nanoscale colloidal dispersions. High and low energy methods are used to prepare nanoemulsions, including high pressure homogenization, ultrasonication, phase inversion temperature and emulsion inversion point, as well as recently developed approaches such as bubble bursting method. In this review article, we summarize the major methods to prepare nanoemulsions, theories to predict droplet size, physical conditions and chemical additives which affect droplet stability, and recent applications.Eni S.p.A

Charge injection from carbon nanofibers into hexane under ambient conditions

The observation of charge injection from carbon nanofibers (CNFs) into liquid hexane under ambient conditions is reported. A CNF-coated electrode and a counter electrode are brought into micrometer proximity in a quasi-parallel geometry using a strain-gauge-based proximity sensor. Controlled charge injection is obtained at interelectrode distances of 4, 6, 9, and 15 μm. The resulting emission current shows an onset of about 3 V/μm , and it follows the Fowler-Nordheim behavior. The work reported here opens new applications for free electron chemistry in liquids and novel liquid field emitter devices

An Edible Humidity Indicator That Responds to Changes in Humidity Mechanically

Elevated humidity levels in medical, food, and pharmaceutical products may reduce the products' shelf life, trigger bacterial growth, and even lead to complete spoilage. In this study, we report a humidity indicator that mechanically bends and rolls itself irreversibly upon exposure to high humidity conditions. The indicator is made of two food-grade polymer films with distinct ratios of a milk protein, casein, and a plasticizer, glycerol, that are physically attached to each other. Based on the thermogravimetric analysis and microstructural characterization, we hypothesize that the bending mechanism is a result of hygroscopic swelling and consequent counter diffusion of water and glycerol. Guided by this mechanism, we demonstrate that the rolling behavior, including response time and final curvature, can be tuned by the geometric dimensions of the indicator. As the proposed indicator is made of food-grade ingredients, it can be placed directly in contact with perishable products to report exposure to undesirable humidity inside the package, without the risk of contaminating the product or causing oral toxicity in case of accidental digestion, features that commercial inedible electronic and chemo-chromatic sensors cannot provide presently.</p

A review on laser-induced crystallization from solution

Crystallization is abound in nature and industrial practice. A plethora of indispensable products ranging from agrochemicals and pharmaceuticals to battery materials, are produced in crystalline form in industrial practice. Yet, our control over the crystallization process across scales, from molecular to macroscopic, is far from complete. This bottleneck not only hinders our ability to engineer the properties of crystalline products essential for maintaining our quality of life but also hampers progress toward a sustainable circular economy in resource recovery. In recent years, approaches leveraging light fields have emerged as promising alternatives to manipulate crystallization. In this review article, we classify laser-induced crystallization approaches where light-material interactions are utilized to influence crystallization phenomena according to proposed underlying mechanisms and experimental setups. We discuss non-photochemical laser-induced nucleation, high-intensity laser-induced nucleation, laser trapping-induced crystallization, and indirect methods in detail. Throughout the review, we highlight connections amongst these separately evolving sub-fields to encourage interdisciplinary exchange of ideas.Comment: V. Korede and N. Nagalingam contributed equally to this wor

Laser-Induced Cavitation for Controlling Crystallization from Solution

We demonstrate that a cavitation bubble initiated by a Nd:YAG laser pulse below breakdown threshold induces crystallization from supersaturated aqueous solutions with supersaturation and laser-energy dependent nucleation kinetics. Combining high-speed video microscopy and simulations, we argue that a competition between the dissipation of absorbed laser energy as latent and sensible heat dictates the solvent evaporation rate and creates a momentary supersaturation peak at the vapor-liquid interface. The number and morphology of crystals correlate to the characteristics of the simulated supersaturation peak

Universal motion of mirror-symmetric microparticles in confined Stokes flow

Comprehensive understanding of particle motion in microfluidic devices is essential to unlock novel technologies for shape-based separation and sorting of microparticles like microplastics, cells and crystal polymorphs. Such particles interact hydrodynamically with confining surfaces, thus altering their trajectories. These hydrodynamic interactions are shape-dependent and can be tuned to guide a particle along a specific path. We produce strongly confined particles with various shapes in a shallow microfluidic channel via stop flow lithography. Regardless of their exact shape, particles with a single mirror plane have identical modes of motion: in-plane rotation and cross-stream translation along a bell-shaped path. Each mode has a characteristic time, determined by particle geometry. Furthermore, each particle trajectory can be scaled by its respective characteristic times onto two master curves. We propose minimalistic relations linking these timescales to particle shape. Together these master curves yield a trajectory universal to particles with a single mirror plane.Comment: 10 pages, 4 figures, 1 table, 1 PDF file containing Supplementary Text, Figures and Tabl