A multipoint quasi-distributed optical fiber pH sensor

This paper reports the development and characterisation of a multipoint quasi-distributed optical fiber sensor for pH measurement. The system is based on a 170 m length of 200 μm core diameter plastic cladding silica fiber where sections of cladding have been removed and replaced with dye immobilised sol-gel glass to form sensing points. Evanescent wave excitation of a dye, immobilised within 2 mm long sections of cladding, enables the pH value of any spillage material to be determined by optical time domain reflectometry along the length of the fiber. The results suggest a spatial resolution of better than 2.5 meters for this fiber system and indicate that this arrangement could form the basis of a practical sensor/actuator system for chemical spillage, provided that suitable dye/analyte combinations are available.     

Passive Scalar Transport in a Turbulent Mixing Layer

This paper describes a combined experimental and numerical study of scalar transport in spatially developing, two-stream, turbulent mixing layers with velocity ratios of approximately 2:1. The experimental mixing layer was created by an S-shaped splitter plate mounted in a wind tunnel, and the concentration field was realized by releasing incense smoke into the high-speed side boundary layer above the splitter plate. Simultaneous measurements of the velocity and concentration fields were performed. A 12-sensor hot-wire probe was used to measure the velocity field and its gradients, while the concentration field was recorded with digital photographs of the laser-illuminated smoke. In parallel, a large-eddy simulation (LES) of the spatially developing mixing layer was carried out. Auxiliary turbulent boundary layer LES were used to provide high quality inflow boundary conditions for the velocity and concentration fields. By synchronizing the velocity and concentration measurements, concentration fluxes were also determined. Octant analysis based on the sign combinations of the velocity and concentration fuctuations was performed on the flux data to investigate the scalar transport processes. It was found that octants compatible with mean gradient transport of the scalar contribute most to the scalar fluxes. Conditional planar averages of scalar and momentum fluxes were obtained to determine their spatial distribution with respect to the organized roller and rib vortices of the mixing layer, and distinct patterns were observed. The simulation provided additional insight about the flow and scalar flux distribution topology. This topology was found to be partially compatible with simple models of roller and rib vortices that transport the scalar in a mean gradient sense.     

Electrochemical methods for analysing and controlling charge transfer at the electrode–tissue interface

There have been rapid advances in the development of new materials for use in electrode–tissue interfacing. The development of conducting polymers, conducting hydrogels, carbon nanotubes, graphene and other conducting materials has provided a rich landscape for controlling charge transfer at the electrode–tissue interface and hence to monitor and manipulate cell behaviour. These materials have been used in tissue-engineered constructs to direct and control cell proliferation, growth and differentiation. However, their translation to clinical devices has been less successful. In this review, the use of electroanalytical techniques to develop an understanding of charge transfer at the electrode–tissue interface is discussed. In particular, the impact of solution and electrode conditions on charge injection capacity is demonstrated. The importance of standardised testing methods and the correlation of electrochemical and electrophysiological performance show the limitations of empirical studies and help define key electrode properties for clinical devices. The development of a sound theoretical basis for charge transfer at this increasingly important interface is being advocated to improve clinical outcomes and device lifetime and reduce power usage.     

Phospholipid lung surfactant and nanoparticle surface toxicity: Lessons from diesel soots and silicate dusts

Because of their small size, the specific surface areas of nanoparticulate materials (NP), described as particles having at least one dimension smaller than 100 nm, can be large compared with micrometer-sized respirable particles. This high specific surface area or nanostructural surface properties may affect NP toxicity in comparison with micrometer-sized respirable particles of the same overall composition. Respirable particles depositing on the deep lung surfaces of the respiratory bronchioles or alveoli will contact pulmonary surfactants in the surface hypophase. Diesel exhaust ultrafine particles and respirable silicate micrometer-sized insoluble particles can adsorb components of that surfactant onto the particle surfaces, conditioning the particles surfaces and affecting their in vitro expression of cytotoxicity or genotoxicity. Those effects can be particle surface composition-specific. Effects of particle surface conditioning by a primary component of phospholipid pulmonary surfactant, diacyl phosphatidyl choline, are reviewed for in vitro expression of genotoxicity by diesel exhaust particles and of cytotoxicity by respirable quartz and aluminosilicate kaolin clay particles. Those effects suggest methods and cautions for assaying and interpreting NP properties and biological activities.     

Anion sensing 'venus flytrap' hosts: a modular approach

A series of podands based on three hydrogen bonding 'arms' have been prepared and their affinities for simple inorganic anions measured.     

Large amplitude vibration in polyatomic molecules. I. A polar representation of orthogonal relative coordinates

A general expression for the rovib kinetic energy operator in a system of orthogonal internal coordinates is derived for arbitrary amplitudes of motion. Plots of the molecular potential in such coordinates serve to determine coordinate subsets in which the potential approaches separability. A revision of previous theory for the three-body problem is presented. A rovib hamiltonian for non-branched four-atom molecules (such as C₂H₂) is derived. Certain features of application to polyatomic (five-atom) molecules are considered.     

Evaluation of methods for determining the refraction correction for light-scattering photometers

Recent literature reports from three laboratories have treated the refraction correction for the Sofica and a noncommercial light scattering photometer. Our re-evaluation of the data contained in these reports, as well as our experiments, indicate that the usually cited n² refraction correction has not been unquestionably established for these instruments. In some cases, imprecise experimental techniques have been used to support this particular form of the correction. In addition, we find the optical system of the Sofica instrument results in the detector seeing vertically past the horizontal edge of the illuminated volume in violation of a basic assumption in the deduction of the n² correction. Our experiments, as well as our interpretation of recent literature data, support an exponent of less than 2.0 for the Sofica apparatus, which is consistent with an instrument whose detector views outside the illuminated volume. However, the experimental methods available to evaluate the exponent lack the desired precision.