Colloidal single crystals of silica spheres in the presence of simple- and poly-electrolytes,and ionic detergents

Colloidal single crystals of silica spheres (103 nm in diameter) are formed in the presence of various kinds of salts 1 simple electrolytes, i.e., sodium chloride, calcium chloride and lanthanum chloride, 2 polyelectrolytes such as 3–6 type ionen polymer (polybrene), poly-N-ethylpyridinium bromide, a copolymer ofN-benzyl pyridinium chloride andN-hexadecyl pyridinium bromide, and sodium polyethylene sulfonate, and 3 cationic and anionic detergents, hexadecyltrimethylammonium bromide and sodium dodecylsulfate. Shape and size of their single crystals, phase diagram, and the relationship between the two parameters among the critical concentration of melting, conductance and pH of the crystal-like suspensions have been studied. Colloidal single crystals ofpositively charged spheres have been formed in this study by the method of the charge reversal of spheres through the strong adsorption of cationic polyelectrolytes onto the anionic silica spheres.     

Electron microscopic study on nucleation and growth of silver particles in a thin glass film

Nucleation and crystal growth of silver particles in a thin glass film of Li₂O·2.6SiO₂ glass containing 0.1 wt% of Ag₂O were observed by transmission electron microscopy and studied by an electron diffraction technique. Anomalies of the image contrast which appeared in the heat-treated specimens were explained to be caused by phase separation of the glass. Nucleation of silver particles was found to occur on the surface of the phase-separated silica-rich droplets. As the silver particles grew, their shape changed into that of a regular cube which was covered with a thin diffusion layer of silver ions about 50 Å in thickness. The presence of this thin layer and the cubic shape suggest that the growth of silver particles proceeds by a layer-by-layer growth mechanism.     

Soft-x-ray harmonic comb from relativistic electron spikes

We demonstrate a new high-order harmonic generation mechanism reaching the "water window" spectral region in experiments with multiterawatt femtosecond lasers irradiating gas jets. A few hundred harmonic orders are resolved, giving μJ/sr pulses. Harmonics are collectively emitted by an oscillating electron spike formed at the joint of the boundaries of a cavity and bow wave created by a relativistically self-focusing laser in underdense plasma. The spike sharpness and stability are explained by catastrophe theory. The mechanism is corroborated by particle-in-cell simulations.     

High-contrast, high-intensity laser pulse generation using a nonlinear preamplifier in a Ti:sapphire laser system

We report a high-contrast, high-intensity Ti:sapphire chirped-pulse amplification system that incorporates a nonlinear preamplifier based on optical parametric chirped-pulse amplification (OPCPA). By cooling the Ti:sapphire crystal in the final amplifier down to 77 K, the chirped-pulses are amplified to 2.9 J at a 10 Hz repetition rate without a thermal lensing effect. Pulse compression down to 19 fs duration obtained after amplification indicates a peak power of 80 TW. With the OPCPA, the temporal contrast is significantly improved to better than 7x10(-9) in a few picoseconds interval prior to the main laser pulse.     

Measurement of tritium in tree rings: Isolation of α-cellulose from wood chips using explosive depressurization

Explosive depressurization offered an effective pre-treatment for isolating -cellulose from wood chips using the common chlorite method. This operation shortened the time required for isolation of -cellulose of relatively high purity by up to 6 h, and raised the relative crystallinity of the product to 65–72% from 50% or below for the unexploded samples. The steam-explosion was carried out by combining 2 min of pre-hydrolysis at a pressure of 3.55 MPa with a rapid decompression. This was found to be the best operating condition for pine wood chips of 1 mm thickness to analyze the tritium content in tree rings accurately.     

Application of anion-exchange techniques to the determination of traces of molybdenum in sea-water

A combined ion-exchange spectrophotometric method has been developed for the determination of molybdenum in sea-water. Molybdenum is sorbed strongly on Amberlite CG 400 (Cl(-)) at pH 3 from sea-water containing ascorbic acid and is easily eluted with 6M nitric acid. Molybdenum in the effluent can be determined spectrophotometrically with potassium thiocyanate and stannous chloride. The combined method allows selective and sensitive determination of traces of molybdenum in sea-water. The precision of the method is 2% at a molybdenum level of ~ 10 mug l .     

Determination of uranium and thorium in phosphate rocks by a combined ion-exchange — Spectrophotometric method

Summary Determination of Uranium and Thorium in Phosphate Rocks by a Combined Ion-Exchange — Spectrophotometric Method A selective anion-exchange separation and Spectrophotometric method has been developed for the determination of uranium and thorium in phosphate rocks. About 0.2 g of rock sample is decomposed with nitric acid. Uranium and thorium are adsorbed by anion-exchange on an Amberlite CG 400 (NO₃ ^–) column from the sample solution adjusted to 2.5M in magnesium nitrate and 0.1M in nitric acid. Uranium and thorium are eluted consecutively with 6.6M nitric acid and 0.1M nitric acid, respectively. Uranium and thorium in the respective effluents are determined spectrophotometrically with Arsenazo III. Results are quoted on uranium and thorium in NBS standard phosphate rock and others.     

Theoretical calculation of the reduced viscosity of aqueous suspensions of charged spherical particles

The origin of the variety of characteristics of the reduced viscosity of aqueous suspensions of charged spherical particles has been an unsolved problem. To solve the problem, the reduced viscosity due to interparticle electrostatic interactions between charged spherical particles are calculated as a function of particle concentration with scanning various parameters, such as diameter of particle, number of charges per particle, and added‐salt concentration. The result successfully reproduced the variety of characteristics. Of all the scanned parameters, the diameter of the particle has a significant role to display the variety of characteristics when other parameters are fixed. When the diameter is very small (～0 Å), the calculated reduced viscosity of aqueous suspensions of charged spherical particles increases with decreasing particle concentration and it shows a maximum. This behavior is very similar to the reduced viscosity of linear chain polyelectrolyte solutions. Whereas, when the diameter is large (>2000 Å), the calculated reduced viscosity decreases with decreasing particle concentration and it does not show a maximum. When the diameter is <1000 Å, the calculated reduced viscosity shows both the maximum and minimum. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 1068–1074, 2004     

Effects of the self-absorption of X-ray spectral lines in the presence of the laser-cluster interaction

The effects of self-absorption of X-ray spectral lines have been experimentally observed in the plasma of cluster targets. It has been shown that, since a cluster target is condensed in the femtosecond time scale and gaseous in the picosecond time scale, self-absorption effects can observed for X-ray spectral lines that are predominantly emitted during the action of a laser pre-pulse. The self-absorption effects are manifested as spectral lines with asymmetric profiles where the long-wavelength wing is suppressed compared to the short-wavelength wing. The observation of asymmetric contours is important for the diagnostics of the laser-cluster interaction because it enables the conclusion of whether the laser pre-pulse completely destroys the cluster and makes it possible to quantitatively estimate the size of the central region of the cluster, which has a solid-state density to the moment of the arrival of the main laser pulse.     

The effects of film thickness and incorporated anions on pitting corrosion of aluminum with barrier-type oxide films formed in neutral borate and phosphate electrolytes

The pitting corrosion behavior of high-purity aluminum covered with barrier-type anodic films, which are formed in neutral borate and phosphate electrolytes, has been examined in 0.5 mol dm^?3 NaCl solution at an applied potential of ?0.6 V versus Ag/AgCl, which is slightly nobler than the pitting potential of ?0.64 V in the same solution. The pitting current density, i _p, increased with time after an incubation time, t _i. The double logarithmic plot of i _p and polarization time, t, reveal two straight lines, which are separated at the time, τ. The slope becomes larger after τ for the specimens anodized in the phosphate electrolyte, while it becomes smaller for those in the borate electrolyte. Both the t _i and τ increase with the thickness of the anodic films, and at the similar film thickness, they are much larger for the anodic films formed in the phosphate electrolyte than for those in the borate electrolyte. The corrosion process can be divided into three stages: the incubation period up to t _i, the pit nucleation period before τ, and the pit growth period after τ. We have discussed the different pitting corrosion behavior of the aluminum specimens covered with the anodic films formed in the borate and phosphate electrolytes in terms of ion selectivity of the anodic films.