Dielectrophoresis of nanoparticles

A numerical scheme based on the distributed Lagrange multiplier method (DLM) is used to study the motion of nano-sized particles of dielectric suspensions subjected to uniform and nonuniform electric fields. Particles are subjected to both electrostatic and hydrodynamic forces, as well as Brownian motion. The results of the simulations presented in this paper show that uniform electric fields the evolution of the particle structures depends on the ratio of electrostatic particle-particle interactions and Brownian forces. When this ratio is of the order of 100 or greater, particles form stable chains and columns, whereas when it is of the order of 10 or smaller the particle distribution is random. For the nonuniform electric field cases considered in this paper, the relative magnitude of Brownian forces is in the range such that it does not influence the eventual collection of particles by dielectrophoresis and the particular locations where the particles are collected. However, Brownian motion is observed to influence the transient particle trajectories. The deviation of the particle trajectories compared to those determined by the electrostatic and hydrodynamic forces alone is characterized by the ratio of Brownian and dielectrophoretic forces.     

Dielectrophoresis induced clustering regimes of viable yeast cells

We experimentally study the transient clustering behavior of viable yeast cells in a dilute suspension suddenly subjected to a nonuniform alternating current (AC) electric field of a microelectrode device. The frequency of the applied electric field is varied to identify two distinct regimes of positive dielectrophoresis. In both regimes, the yeast cells eventually cluster at electrodes' edges, but their transient behavior as well as their final arrangement is quite different. Specifically, when the frequency is much smaller than the cross-over frequency, the nearby yeast cells quickly rearrange in well-defined chains which then move toward the electrodes' edges and remain aligned as elongated chains at their final location. However, when the frequency is close to the cross-over frequency, cells move individually toward the regions of collection and simply agglomerate along the electrodes' edges. Our analysis shows that in the first regime both the dielectrophoretic (DEP) force and the mutual DEP force, which arises due to the electrostatic particle-particle interactions, are important. In the second regime, on the other hand, the DEP force dominates.     

Identification of a novel series of alkylitaconic acids in wood cultures of Ceriporiopsis subvermispora by gas chromatography/mass spectrometry.

A novel series of long-chain unsaturated dicarboxylic acids consisting of a long aliphatic chain attached to the C-3 position of itaconic acid has been identified by gas chromatography/mass spectrometry during in vitro decay of eucalypt wood by the white-rot basidiomycete Ceriporiopsis subvermispora. The major compounds were identified as tetradecyl-, 7-hexadecenyl- and hexadecylitaconic acids by their mass fragmentation patterns. Other members of the same compound series, identified as dodecanyl-, tridecanyl-, tetradecenyl-, pentadecanyl-, octadecenyl- and octadecanylitaconic acids, were present in very minor amounts or traces. Whereas hexadecenylitaconic acid has already been reported in cultures of C. subvermispora, to our knowledge this is the first report of the presence of the other alkylitaconic acids in fungal cultures. These new alkylitaconic-type metabolites may constitute a source for peroxidizable lipids involved in lignin degradation during wood decay by C. subvermispora and other white-rot basidiomycetes.     

Manipulation of particles using dielectrophoresis

A numerical scheme based on the distributed Lagrange multiplier method (DLM) is used to study the motion of particles of electrorheological suspensions subjected to non-uniform electric fields. At small Reynolds number, the time taken by the particles to collect at the minimums or maximums of the electric field is primarily determined by a parameter defined to be the ratio of the dielectrophoretic and viscous forces. Simulations show that in non-uniform electric fields the collection time is also influenced by a parameter defined by the ratio of the electrostatic particle–particle interaction and dielectrophoretic forces. The collection time decreases as this parameter decreases because when this parameter is less than one, particles move to the regions of high or low electric field regions individually. However, when this parameter is greater than one, particles regroup into chains which then move toward the electric field maximums or minimums without breaking. It is also shown that when the real part of the Clausius–Mosotti factor (β) is negative the positions of the local minimums of the electric field, and thus also the locations where particles collect, can be modified by changing the electric potential boundary conditions.     

Permeability of periodic arrays of spheres

For periodic arrays of spheres the permeability is obtained numerically as a function of the dimensionless wave number kD in the flow direction, where D is the sphere diameter, k = 2π/λ is the wave number, and λ is the distance between the spheres in the flow direction. Our numerical results for the solids fraction of 0.45 show that for kD < 6.5 the permeability increases with increasing kD. But, it decreases for 6.5 < kD < 8.5 and reaches a local minimum at kD  8.5, and then increases again with increasing kD. Since the Fourier spectrum of the area fraction is zero for kD = 8.98, this result suggests that the area fraction plays an important role in determining the dependence of permeability on the distance between the spheres in the flow direction. For smaller solids fractions, the positions of the local maximum and minimum of permeability shift to slightly smaller kD’s.     

Quenching of giant hysteresis effects in La(1-z)Y(z)Hx switchable mirrors

Hydrogen atoms adsorbed on TiO2(110)-(1x1) surfaces have been characterized by scanning tunneling microscopy (STM) combined with electron stimulated desorption (ESD) technique. Certain amounts of H atoms are unexpectedly found on the TiO2 surfaces annealed at 900 K. Two forms of adsorption were discriminated in STM images from the different sensitivity to ESD and tentatively assigned to hydroxyl-type (O-H) and hydride-type (Ti-H) species.