Speed of flame propagation in CH<Subscript>3</Subscript>Cl + Cl<Subscript>2</Subscript> mixtures during combustion initiated by continuous UV radiation

Flame propagation in a closed tube over mixtures of chloromethane and chlorine of different compositions following ignition by continuous UV radiation is studied. It is found that the rate of combustion in all mixtures except limiting ones grows along with the propagation of the flame front up to its maximum values at nearly 1/3 the tube length and then slows. In limiting mixtures, the speed’s behavior is completely different. It is greatest near the source of UV light and gradually slows with distance from the source. The high speed in the initial section is due to the effect of UV light. The temperature of combustion is lowest in limiting mixtures, and the rate of chlorine molecule photodissociation at this temperature is comparable to and even faster than that of their thermal dissociation. The light in these mixtures thus contributes substantially to the initiation of the chemical reaction. It is concluded that when limiting mixtures are ignited by UV pulses, the speed of flame propagation falls markedly as it proceeds without the influence of radiation, and the character of changes in the speed’s behavior becomes identical to those for other mixtures.     

Inhibition of the photoinduced ignition of chloromethane–chlorine mixtures by oxygen

The introduction of small amounts of oxygen inhibits the photoinduced ignition of chloromethane–chlorine mixtures. This is accompanied by an increase in the induction period and a decrease in the degree of heating of the reaction mixture. After the consumption of the entire inhibitor, the photochlorination reaction takes place again in the thermal explosion regime but with a lower degree of heating. In the dependence of the mixture temperature on the oxygen concentration, criticality is not pronounced. With an increasing concentration of oxygen, its effect on the induction period weakens.     

System of cryostating wide-aperture nonlinear crystals for generating the fifth harmonic of neodymium-laser radiation

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 51, No. 5, pp. 867–870, November, 1989.     

Copolymerization of N,N-diallyl-N′-benzoylhydrazine with acrylonitrile and sulfur dioxide

Radical copolymerization of N,N-diallyl-N′-benzoylhydrazine with acrylonitrile and sulfur dioxide was studied. The kinetic features of the copolymerization of these systems were examined, the relative activities of the monomers were determined, and the structure of the resulting copolymers was elucidated.     

Existence of Periodic Solutions of a Third-Order Nonlinear System

Differential Equations - We consider a nonlinear autonomous third-order ODE system depending on numerical parameters and describing the motions of an energy harvester that converts residual thermal...     

Time-resolved measurements of hot-electron equilibration dynamics in high-intensity laser interactions with thin-foil solid targets

Time-resolved K(α) spectroscopy has been used to infer the hot-electron equilibration dynamics in high-intensity laser interactions with picosecond pulses and thin-foil solid targets. The measured K(α)-emission pulse width increases from ~3 to 6 ps for laser intensities from ~10(18) to 10(19) W/cm(2). Collisional energy-transfer model calculations suggest that hot electrons with mean energies from ~0.8 to 2 MeV are contained inside the target. The inferred mean hot-electron energies are broadly consistent with ponderomotive scaling over the relevant intensity range.     

Optical properties of laser plasma produced by pulses of different duration

The results of experiments on the interaction of laser radiation pulses (at intensities of up to 1015 W cm−2) of different durations (t = 3ps; 300ps; 30ns) with targets in a vacuum chamber are presented. An investigation was made of the optical characteristics of laser plasma in vacuum ultraviolet and X-ray ranges. The intensity of the laser-produced plasma radiation in the range 1–50nm was estimated to be 1010–1012W cm−2. This revised version was published online in November 2006 with corrections to the Cover Date.     

High-contrast optical-parametric amplifier as a front end of high-power laser systems

A high-contrast preamplifier based on optical-parametric amplification with a short pump pulse is demonstrated. A gain larger than 10(5) and measurement-limited contrast higher than 10(11) are obtained over a large temporal range extending within less than 10 ps of the peak of the pulse, because of the high instantaneous parametric gain provided by a short pump pulse in a nonlinear crystal. The energy gain and high contrast of this preamplifier make it a good seed source for high-power laser systems.     

High-conversion-efficiency optical parametric chirped-pulse amplification system using spatiotemporally shaped pump pulses

High-conversion-efficiency, high-stability optical parametric chirped-pulse amplification is demonstrated with a spatiotemporally shaped pump laser system. Broadband 5-mJ pulses are produced at a 5-Hz repetition rate with a pump-to-signal conversion efficiency of 29% and energy stability better than 2% rms. To our knowledge this is the highest conversion efficiency and stability achieved in an optical parametric chirped-pulse amplification system.     

Copolymerization of N-vinylpyrrolidone with N-allylated acylhydrazines

The free-radical copolymerization of N-vinylpyrrolidone with N,N-diallyl-N′-acetylhydrazine and N,N-diallyl-N′-butanoylhydrazine has been investigated in bulk and solution. The copolymerization yields random copolymers enriched with N-vinylpyrrolidone units. The kinetic study of the reaction has revealed that the rate of copolymerization decreases with a rise in the fraction of an allyl monomer in the initial monomer mixture. Both double bonds of diallylacylhydrazines are involved in the copolymerization to give rise to five-membered pyrrolidine rings.