Contour lines of the optical functions for solids

The well-known equations for the optical functions of reflectance, transmittance and phase changes on reflection and transmission for a solid material have been rearranged into the form of simple geometric figures in the u, v (n, k) plane. The curves for F_p show a singularity on the n-axis.     

A Device to Provide Respiratory-Mechanical Unloading

A commercially available and widely used servo-controlled ventilator has been modified to provide controlled inspiratory resistive unloading of the human respiratory system. This is achieved by establishing a positive mouth pressure throughout inspiration in a constant proportion to instantaneous flow, i.e., the ratio of mouth pressure to flow, which defines the "assistance," remaining constant. The performance of this device has been evaluated in four healthy subjects during steady-state, constant-load cycling (20-120 W). It is demonstrated that i) the device can successfully implement controlled degrees of inspiratory assistance on a breath-to-breath basis; ii) the assistance can be sustained over a substantial range of ventilatory drive (i.e., for ventilations up to some 30 1/min) and to an extent which approaches a 100 percent reduction of the normal respiratory resistance. This device should prove useful in experimental and clinical investigations of the respiratory responses to resistive unloading of the respiratory system.     

Rapid multielemental analysis of Chinese reference soils by laser ablation inductively coupled plasma-source mass spectrometry

Summary Laser ablation inductively coupled plasma-source mass spectrometry has been used to determine thirty elements (Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, As, Rb, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Dy, Ho, Yb, Hf, Ta, W, Th, U) in seven Chinese reference soils. The Surrey prototype spectrometer was employed with sample ablation by a free-running ruby laser. Concentrations in the soils (GSS-2 to GSS-8) were calculated from elemental responses and sensitivities derived from another soil in the series, namely GSS-1. Comparisons with previous neutron activation analyses are made. Rapid semiquantitative analyses are proved feasible. About eighty percent of the LA-ICP-MS determined concentrations were within a factor of two of the concentrations measured by INAA, and many were considerably closer than this. Precisions were typically in the range 2–10% RSD, but some were considerably poorer for elements present at trace levels.     

OR turnaround: looking at problem areas

This is the fourth in a series on management strategies for "turning around an OR." The first three articles appeared in the January, April, and June issues of OR Manager.     

The search for organically bonded iron in New Zealand brown coals

Brown coal from two areas in New Zealand was treated with acids (HF and HCl) to remove the clays. Iron was then introduced into the “cleaned” coal by ion exchange. Mössbauer spectra of the untreated coal, the low temperature ash of the coal, “cleaned” coal and ion-exchanged coal were analysed. From these spectra we conclude that a pair of lines with QS～1 mm s^?1 and IS～0.45 mm s^?1 is probably due to organically bonded iron.     

Kaon production in\bar pp interactions at c.m. energies from 200 to 900 GeV

A detailed analysis ofK _s ⁰ production in \(\bar pp\) |<2.5 the average transverse momentum is found to be 0.53±0.07 GeV/c at 200 GeV and 0.62±0.08 GeV/c at 900 GeV, which is an increase with respect to data at c.m. energies below 60 GeV. TheK _s ⁰ production cross sections in inelastic collisions are 29±4 mb at 200 GeV and 63±6 mb at 900 GeV, showing an increase compared to lower energy data. The central kaon density is found to increase as a logarithmic function of energy. At 900 GeV, where statistics are sufficient to allow one to draw conclusions, the average transverse momentum is higher in events with large charged multiplicity than in events with low multiplicity.     

Nucleophilic substitution by arenethiolates at the carbene carbon of pentacarbonyl(methoxymethylcarbene)-metal(o) complexes (metal = Cr,Mo, or W)

The phenylthiocarbene complexes, [(CO)₅MC(CH₃)(SPh)] (M = Cr, Mo, or W) have been prepared in good yield by the reaction of [(CO)₅MC(CH₃)(OCH₃)] (M = Cr, Mo, or W) with NaSPh in benzene/methanol in the presence of HCl. A series of para-substituted phenylthiocarbene complexes of tungsten. [(CO)₅WC(CH₃)SC₆H₄Y)], (Y = p-Br, p-F, p-H, p-CH₃, p-OCH₃ or p-OH) have also been prepared by the reaction of the appropriate arenethiolate ion with [(CO)₅WC(CH₃)(OCH₃)]. Poor nucleophiles such as p-nitrobenzenethiolate and pentafluorobenzenethiolate did not react with [(CO)₅WC(CH₃)(OCH₃) to form the corresponding phenylthiocarbene complex. A mechanism accounting for the formation of these phenylthiocarbene complexes is proposed. The complexes have been characterized by their infrared, electronic, mass, ¹H NMR, and ¹³C NMR spectra. These spectroscopic data have been used to establish the structure of these complexes in solution and indicate that the phenyl ring bonded to sulfur is probably not coplanar with the “carbene” plane.