PII: S 0 0 4 0 -6 0 9 0 Ž 0 3 . 0 0 0 2 9 -4 In situ measurements of sensor film dynamics by spectroscopic ellipsometry. Demonstration of back-side measurements and the etching of indium tin oxide

Abstract A new liquid flow cell design for in situ ellipsometric measurements on transparent multilayer samples using variable angle spectroscopic ellipsometry is presented. In this cell, films made on transparent substrates are in direct contact with liquid solution. Ellipsometry measurements are made through the transparent substrate, that is, from the back-side relative to the incident light so that films are in continuous contact with the liquid. This cell is not limited to just one angle of incidence of light allowing the films to be characterized at several angles before, during and after liquid contact. The spectral range of measurements is limited only by absorption of light in the underlying transparent substrate and not by the liquid solution that the film is in contact with. As a demonstration, we have measured and analyzed the dynamics of an indium tin oxide film on glass undergoing acid etching. Data from this in situ experiment were successfully modeled and the ITO layer thickness decreased uniformly during the etching process with an average etch rate of 0.23 nmymin

Atomic Energy Commission Report NYO-9786

"Helium, nitrogen, carbon dioxide, and other gases suitable as reactor coolants were evaluated. It is shown that because of the helium conservation program, recently authorized by legislation, sufficient helium will become available for domestic power plants and for the requirements of the Euratom group. Tables of thermodynamic properties for helium and molecular nitrogen were computed from the Beattie-Bridgman equation of state. Specific enthalpy, specific entropy, isobaric specific heat, specific heat ratio, compressibility factor, specific volume, and acoustic velocity are tabulated over the range helium and molecular nitrogen are given.

Electrochemical investigation of Pb²⁺ binding and transport through a polymerized crystalline colloidal array hydrogel containing benzo-18-crown-6

The transport of Pb2+ through a sensory gel, a polymerized crystalline colloidal array hydrogel with immobilized benzo-18-crown-6, is important for understanding and optimizing the sensor. Square wave voltammetry at a Hg/ Au electrode reveals many parameters. The partition coefficient for Pb2+ into a control gel (no crown ether), Kp, is 1.00 ± 0.018 (errors reported are SEM). The porosity, ε, of the gel is 0.90 ± 0.01. Log Kc for complexation in the gel is 2.75 ± 0.014. Log Kc in aqueous solution for Pb2+ with the ligand 4-acryloylamidobenzo-18-crown-6 is 3.01 ± 0.010 with dissociation rate kd = (8.34 ± 0.45) × 102 s-1 and association rate kf = (8.79 ± 0.025) × 107 M-1 s-1. The partition coefficient of the ligand 4-acryloylamidobenzo-18-crown-6 into the control gel, K p,L is 2.07 ± 0.15. The diffusion coefficient of Pb 2+ in the control gel is 6.72 × 10-6 ± 0.12 cm2/s. For the sensor gel, but not control gel, diffusion coefficients are location dependent. The range of diffusion coefficients for Pb2+ in the probed locations was found to be (6.11-12.60) × 10-7 cm2/s for 0.91 mM Pb2+ and (2.84-9.39) × 10-7 cm2/s for 0.35 mM Pb2+. Lead binding in the sensor gel is slightly less avid than in solution. This is attributed, in part, to the demonstrated affinity of the ligand 4-acryloylamidobenzo-18-crown-6 to the gel. Diffusion coefficients determined for the sensor gel were found to be location dependent. This is attributed to heterogeneities in the crown concentration in the gel. Analysis of diffusion coefficients and rate constants show that diffusion and not chemical relaxation will limit the time response of the material

Simultaneous maximization of cell permeabilization and viability in single-cell electroporation using an electrolyte-filled capillary

A549 cells were briefly exposed to Thioglo-1, which converts thiols to fluorescent adducts. The fluorescent cells were exposed to short (50-300 ms) electric field pulses (500 V across a 15 cm capillary) created at the tip of an electrolyte-filled capillary. Fluorescence microscopy revealed varying degrees of cell permeabilization depending on the conditions. Longer pulses and a shorter cell-capillary tip distance led to a greater decrease in the cell's fluorescence. Live/dead (calcein AM and propidium iodide) testing revealed that a certain fraction of cells died. Longer pulses and shorter cell-capillary tip distances were more deadly. An optimum condition exists at a cell-capillary tip distance of 3.5-4.5 mu m and a pulse duration of 120-150 ms. At these conditions, > 90% of the cells are permeabilized and 80-90% survive