Extraction of osmium thiocyanate and its separation from ruthenium by polyurethane foam

A detailed investigation of the conditions for formation and extraction of the thiocyanate complex of osmium by polyether-type polyurethane foam is reported. The complex which formed in solution was extracted through the “cation-chelation” mechanism and distribution coefficients of more than 10⁴ were obtained. By using conditions which inhibit the formation of the osmium-thiocyanate complex, it was possible to leave 95% of osmium in the aqueous phase while extracting more than 95% of ruthenium into polyurethane foam.     

A hologram of large field depth

A hologram of an object with field depth greatly exceeding the coherence length has been made with an ordinary gas laser, taking account of the reoccurence of the temporal coherence and its stability dependence on operating time. Only one object beam is used for a number of seperate exposures, so that the full output power is used.     

Nonlinear reaction-diffusion models for interacting populations

This paper proves that several initial-boundary value problems for a wide class of nonlinear reaction-diffusion equations have solutions c_i(x, t), 1 ? i ? N (with c_i(x, t) representing the concentration of the ith species at position x in a set $\text{Ω}$ at time t ? 0), which exist for all t ? 0 and are unique, smooth, nonnegative, and strictly positive for t > 0. The Volterra-Lotka predator-prey model with diffusion (to which the results above are proved to apply) is then studied in more detail. It is proved that any bounded solution of this model loses its spatial dependence and behaves like a periodic function of time alone as t → ∞. It is proved that if the spatial dimension is one or if the diffusion coefficients of the two species are equal, then all solutions are bounded.     

When electron exchange is chemical exchange-assignment of 1H NMR spectra of paramagnetic cobalt(II)-2,2':6'2''-terpyridine complexes

Electron exchange between [Co(terpy)2]3+ and [Co(terpy)2]2+ can be monitored by 1H NMR exchange spectroscopy and allows the cobalt(II) spectra to be fully assigned.     

Ordering of hydrogen bonds in high-pressure low-temperature H2O

The near K-edge structure of oxygen in liquid water and ices III, II, and IX at 0.25 GPa and several low temperatures down to 4 K has been studied using inelastic x-ray scattering at 9884.7 eV with a total energy resolution of 305 and 175 meV. A marked decrease of the preedge intensity from the liquid phase and ice III to ices II and IX is attributed to ordering of the hydrogen bonds in the proton-ordered lattice of the latter phases. Density functional theory calculations including the influence of the Madelung potential of the ice IX crystal correctly account for the remaining preedge feature. Furthermore, we obtain spectroscopic evidence suggesting a possible new phase of ice at temperatures between 4 and 50 K.     

Local structure of isolated positively charged muonium as an analog for the hydrogen ion in p-type GaAs

We determine the local structure of isolated positively charged muonium (Mu+) in heavily doped p-type GaAs based on muon level crossing resonance and zero applied field muon spin depolarization data. These measurements provide the first direct experimental confirmation that Mu+, and by analogy H+, is located within a stretched Ga-As bond. The distances between Mu+ and the nearest neighbor Ga and As atoms are estimated to be 1.83 +/- 0.10 A; and 1.76 +/- 0.10 A, respectively. These results are compared to existing theoretical calculations on the structure of hydrogen in GaAs and additionally provide data on the induced electric field gradients.