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Orlin D Velev

Publications and source records attributed to Orlin D Velev.

18 recordsLinked to original sources

Evaporation-induced particle microseparations inside droplets floating on a chip.

We describe phenomena of colloidal particle transport and separation inside single microdroplets of water floating on the surface of dense fluorinated oil. The experiments were performed on microfluidic chips, where single droplets were manipulated with alternating electric fields applied to arrays of electrodes below the oil. The particles suspended in the droplets were collected in their top region during the evaporation process. Experimental results and numerical simulations show that this microsepration occurs as a result of a series of processes driven by mass and heat transfer. An interfacial tension gradient develops on the surface of the droplet as a result of the nonuniform temperature distribution during the evaporation. This gradient generates an internal convective Marangoni flow. The colloidal particles transported by the flow are collected in the top of the droplets by the hydrodynamic flux, compensating for evaporation through the exposed top surface. The internal flow pattern and temperature distribution within evaporating droplets were simulated using finite element calculations. The results of the simulation were consistent with experiments using tracer particles. Such microseparation processes can be used for on-chip synthesis of advanced particles and innovative microbioassays.

Colloids↗

Formation of polymer microrods in shear flow by emulsification--solvent attrition mechanism.

Rodlike polymer particles could have interesting properties and could find many practical applications; however, few methods for the production of such particles are available. We report a systematic study of a droplet shearing process for the formation of polymer rods with micrometer or submicrometer diameter and a length of up to tens of micrometers. The process is based on emulsification of a polymer solution under shear, combined with solvent attrition in the surrounding organic medium. The droplets deform and elongate into cylinders, which solidify when the solvent transfers to the dispersion medium. Stopped flow experiments allow distinguishing all stages of the mechanism. The results are interpreted on the basis of the theory of droplet elongation and breakup under shear. The effects of the viscosity ratio and shear stress are matched against the theoretical expectations. The method is simple, efficient, and scalable, and we demonstrate how it can be controlled and modified. The experimental parameters that allow varying the rod size and aspect ratio include shear rate, medium viscosity, and polymer concentration. Examples of the specific properties of the polymer rods, including self-organization, alignment in external fields and in fluid flows, and stabilization of bubbles, droplets, and capsules, are presented.

Emulsions↗

An AC electrokinetic technique for collection and concentration of particles and cells on patterned electrodes.

We report an electrohydrodynamic effect arising from the application of alternating electric fields to patterned electrode surfaces. The AC fields were applied to dilute suspensions of latex microspheres enclosed between a patterned silicon wafer and an ITO-coated glass slide in a small chamber. The latex particles became collected in the center of the conductive "corrals" on the silicon wafer acting as bottom electrode. The particle collection efficiency and speed depended only on the frequency and strength of the field and were independent of the material properties of the particles or the electrodes. The leading effect in the particle collection process is AC electrohydrodynamics. We discuss how the electrohydrodynamic flows emerge from the spatially nonuniform field and interpret the experimental results by means of electrostatic and hydrodynamic simulations. The technique allows three-dimensional microfluidic pumping and transport by the use of two-dimensional patterns. We demonstrate on-chip collection of latex particles, yeast cells, and microbes.

Journal Article↗

Ordered silicon nanocavity arrays in surface-assisted desorption/ionization mass spectrometry.

We report here a simple method to generate ordered nanocavity arrays on a Si wafer and use it in surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS). A close-packed SiO2 nanosphere array was first deposited on a low-resistivity Si wafer using a convective self-assembly method. The nanoparticle array was then used as a mask in a reactive ion etching (RIE) process to selectively remove portions of the Si surface. Subsequent sonication removed those physically adsorbed SiO2 nanoparticles and exposed an ordered nanocavity array underneath. The importance of this approach is its capability of systematically varying surface geometries to achieve desired features, which makes detailed studies of the impacts of surface features on the desorption/ionization mechanism feasible. We demonstrated that the in-plane width and out-of-plane depth of the cavities were adjustable by varying etching times, and the intercavity spacing was controllable by varying the number of particle layers deposited. MS detection of small peptides on these substrates showed comparable sensitivity to conventional porous Si substrates (DIOS, desorption/ ionization on porous silicon). The desorption and ionization efficiency of these roughened surfaces exhibited a nonmonotonic relationship to the increased total surface area. Several possible factors contributing to the observed phenomenon are speculated upon. The application of this arrayed surface in metabolite detection of Arabidopsis thaliana root extracts is also demonstrated.

Arabidopsis↗

Role of the micro- and nanostructure in the performance of surface-enhanced Raman scattering substrates assembled from gold nanoparticles.

Highly active and stable substrates for surface-enhanced Raman scattering (SERS) can be fabricated by using colloidal crystals to template gold nanoparticles into structured porous films. The structure-dependent performance of these SERS substrates was systematically characterized with cyanide in continuous flow microfluidic chambers. A matrix of experiments was designed to isolate the SERS contributions arising from nano- and microscale porosity, long-range ordering of the micropores, and the thickness of the nanoparticle layer. The SERS results were compared to the substrate structure observed by scanning electron microscopy (SEM) and optical microscopy to correlate substrate structure to SERS performance. The Raman peak intensity was consistently highest for nanoporous substrates with three-dimensionally ordered micropores, and decreases if the micropores are not ordered or not templated. Removing the nanoscale porosity by fusion of the nanoparticles (without removing the large micropores) leads to a drastic plunge in substrate performance. The peak intensity does not strongly correlate to the thickness of the nanoparticle films. The results make possible the efficient controlled fabrication of stable, reproducible, and highly active substrates for SERS based chemical sensors with continuous sampling.

Adsorption↗

Anisotropic particle synthesis in dielectrophoretically controlled microdroplet reactors.

The miniaturization of chemical and biological processes in microfluidic devices and bioarrays is a major technological achievement. Microchips performing multiphase material synthesis operations could be a future step in this trend of miniaturizing technology. Here we show how electrically controlled chips can be used for the synthesis and manipulation of new types of particles with advanced structure. The method is based on a technique that allows freely suspended droplets and particles to be entrapped and transported using electric fields. The fields that hold and guide the droplets and particles are applied through arrays of electrodes submerged in the oil. Each of the microdroplets suspended on the surface of fluorinated liquid serves as a microscopic reactor, where the particles are formed by solidification of the carrier droplets. Controlled on-chip assembly, drying, encapsulation and polymerization were used to make anisotropic 'eyeball' and striped particles, polymer capsules and semiconducting microbeads.

Anisotropy↗

Foam superstabilization by polymer microrods.

Few foam systems stabilized by solid particles have been reported, and usually the particles have been used in combination with surfactants. We report how foams can be stabilized solely with a new class of anisotropic particles, hydrophobic polymer microrods of diameter less than 1 mum and length of a few tens of micrometers. The obtained foams were extraordinary stable, retaining a constant volume over many days and even surviving drying of most of the free liquid. The bubbles in these foams were sterically stabilized by dense thick "hairy" layers. The rigid intertwined protective shells around the bubbles did not allow the formation of thin films between them. The lifetime of these foams was orders of magnitude longer than the ones stabilized with typical foaming surfactants such as sodium dodecyl sulfate. The addition of sodium dodecyl sulfate led to hydrophilization of the microrods and suppressed the superstabilization effect. Thus, common foaming agents effectively act as defoamers for the ultrastable foams stabilized by microrods.

Letter↗

Cooling effects on a model rennet casein gel system: part I. Rheological characterization.

The gelation of a model rennet casein system was studied during cooling at different rates. During cooling, casein network structure development was proposed to evolve over a few steps at different length scales: molecules, particles, flocs, or network. Rennet casein flocs are fractal in nature, and fractal dimension and floc size are two variables affecting the rheology and microstructure of a rennet casein gel. Casein structure formation during cooling from 80 to 5 degrees C at four different rates (0.5, 0.1, 0.05, and 0.025 degrees C/min) was monitored by dynamic rheological tests, and a stronger gel developed at a slower cooling rate. During different cooling schedules, similar fractal dimensions were observed due to a lack of difference in the colloidal interactions. Differences among rheological data were possibly caused by variability in floc size, as observed in the second part of this paper. A larger number of smaller-sized flocs enabled gelation at a higher temperature and created a stronger network at a slower cooling rate. Controlling cooling schemes thus provides an approach for manipulating casein gelation and the microstructure for a system of fixed chemical compositions.

Journal Article↗

Cooling effects on a model rennet casein gel system: part II. Permeability and microscopy.

Microscopy and permeability studies were performed to further illustrate the cooling effects on rennet casein gel structure and help interpret the rheological observations in the first part of this paper. Samples of gels cooled from 80 to 5 degrees C at four rates (0.5, 0.1, 0.05, and 0.025 degrees C/min) were studied with a confocal laser scanning microscope. A larger number of smaller flocs were generated at slower cooling rates, creating more cross-links within a network and corresponding to a stronger gel. Formation of a larger number of smaller flocs was hypothesized to result from a greater degree of doublet formation because the system spent more time within the temperature region where doublet formation is favored when cooled at slower rates. The doublets represent sites available for floc growth, similar to nucleation sites for crystal growth. Microscopy results further substantiated that the cooling effects were different from the aging effects because cooling affected floc size, and aging enabled the addition of idle flocs into the casein network. The conclusions for the cooling effects on floc size were further supported by permeability tests. A smaller permeability coefficient resulted from smaller flocs obtained with a slower cooling schedule. This study showed the importance of controlling floc numbers to modulate the strength of a gel, and cooling rates provide an approach of modulating functional properties when the chemical composition of a system is fixed.

Journal Article↗

Fabrication of "hairy" colloidosomes with shells of polymeric microrods.

Novel colloidosome microcapsules with aqueous gel cores and integral shells of rodlike polymeric particles have been prepared and characterized. The synthesis is based on templating water-in-oil emulsions stabilized by rodlike particles followed by gelling of the aqueous phase, dissolution of the oil phase in ethanol, and redispersion of the obtained colloidosome capsules in water. Such capsules may find applications as vehicles for delivery and controlled release of drugs, cosmetics, and food supplements.

Journal Article↗

Controlled, rapid deposition of structured coatings from micro- and nanoparticle suspensions.

The objective of the study was to develop the operational basis for rapid and controlled deposition of crystal coatings from particles of a wide size range. We deposited such structured coatings by dragging with constant velocity a small volume of liquid confined in a meniscus between two plates. Two types of structured coatings were characterized: latex colloidal crystals and thin layers from metallic nanoparticles. The crystal deposition was sped up by use of preconcentrated suspensions. Crystal coatings larger than a few square centimeters were deposited in minutes from aqueous suspension volumes of approximately 10 microL. The governing mechanism of crystal deposition is convective assembly at high volume fractions. The two major process parameters that allow control over the coating thickness and structure were the deposition speed and particle volume fraction. The evaporation rate was not found to affect the process to a large extent. A volumetric flux balance was used to relate the deposition parameters to coating structure and properties. Operational "phase" diagrams were constructed, relating the crystal layer thickness and packing symmetry to the process parameters. These diagrams could be instrumental in transforming the convective colloidal deposition into a robust scaleable technology.

Journal Article↗

Two-dimensional crystallization of microspheres by a coplanar AC electric field.

The particle-field and particle-particle interactions induced by alternating electric fields can be conveniently used for on-chip assembly of colloidal crystals. Two coplanar electrodes with a millimeter-sized gap between them are used here to assemble two-dimensional crystals from suspensions of either latex or silica microspheres. When an AC voltage is applied, the particles accumulate and crystallize on the surface between the electrodes. Light diffraction and microscopic observations demonstrate that the hexagonal crystal is always oriented with one axis along the direction of the field. The particles disassemble when the field is turned off, and the process can be repeated many times. The diffraction patterns from all consecutively formed crystals are identical. This assembly is driven by forces that depend on the electric field gradient, and a model is proposed involving a combination of dielectrophoresis and induced dipole chaining. The organization of large two-dimensional crystals allows characterization of the electrostatic interactions in the particle ensembles. The process can be controlled via the field strength, the frequency, and the viscosity of the liquid media. It could be used to make rudimentary optical switches or to separate mixtures of particles of different sizes.

Journal Article↗

Control and modeling of the dielectrophoretic assembly of on-chip nanoparticle wires.

Suspensions of metallic nanoparticles in water were assembled via the action of an alternating electric field (dielectrophoresis) into wires of micrometer thickness. Two modes of microwire assembly, one through the bulk of the suspension and one as half-cylinders on the glass surface between the electrodes, were identified. The operating conditions responsible for the two assembly modes were recognized. The control of the process parameters allows making, for example, straight single connectors or massively parallel arrays of microwires on the surface of the chip, which can be extracted in dry form. The microwire assembly process was modeled using finite element electrostatic calculations. The direction of growth can be guided by introducing conductive islands or particles in the suspension. The experiments, supported by electrostatic calculations, show that the wires grow in the direction of highest field intensity, "automatically" making electrical connections to the objects between the electrodes. The results point the way to controlled dielectrophoretic assembly of nanoparticles into on-chip electrical connectors, switches, and networks.

Journal Article↗

Effect of pH and Ca2+-induced associations of soybean proteins.

An experimental procedure was developed to characterize the solubility of the soybean protein fractions close to the isoelectric point. The results show that the 7S fraction is precipitated in a much narrower range of pH values than the 11S fraction. Surprisingly, the addition of salt to the solutions leads to increased solubility of proteins, unlike the common "salting out" effect generally expected for proteins in solution in this range of salt concentrations. The precipitation equilibria of both soybean fractions in the presence of calcium ions and electrolyte were characterized. The amount of calcium ions required to precipitate a mole of the 7S fraction is much larger than that required for the 11S fractions. The precipitation pattern can be correlated to the charge density per surface area of the proteins.

Calcium↗