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1.
Studies of breakdown threshold intensity for air at various pressures in the range of 24–760 torr using 0.355, 0.532 and 1.06
μm radiation are reported. We observep
−0.8 scaling ofI
th at 1.06 μm and a weak scaling ofp
−0.4 at 0.532 and 0.355 μm radiation. Strong dependence of breakdown spot size on laser power but weak dependence on air pressure
is observed. 相似文献
2.
Physically meaningful solutions of the field equations for static spherical dust distributions in the Einstein-Cartan theory have been obtained. There is one in which the spin is zero at the center and another with zero spin at the boundary of the sphere. 相似文献
3.
4.
B. S. Narwade P. G. Gawali Rekha Pande G. M. Kalamse 《Journal of Chemical Sciences》2005,117(6):673-676
Dielectric constant (ε’) and dielectric loss (ε") of n-propyl alcohol (PA), ethylenediamine (EDA) and their binary mixtures,
for different mole fractions of ethylenediamine have been experimentally measured at 11.15 GHz microwave frequency. Values
of density (ρ), viscosity (η) and square refractive index (n
D
2
) of binary mixtures as well as those of pure liquids are reported. Excess square refractive index, viscosity and activation
energy of viscous flow have also been estimated. These parameters have been used to explain the formation of complexes in
the system. 相似文献
5.
High pressure behavior of alpha-hydroquinone (1,4-dihydroxybenzene) has been studied using Raman spectroscopy up to pressures of 19 GPa. Evolution of Raman spectra suggests two transitions around 3.3 and 12.0 GPa. The first transition appears to be associated with the lowering of crystal symmetry. Above 12.0 GPa, Raman bands in the internal modes region exhibit continuous broadening suggesting that the system is progressively evolving into a disordered state. This disorder is understood as arising due to distortion of the hydrogen-bonded cage across the second transition around 12 GPa. 相似文献
6.
Single-column ion-chromatography (SCIC) was investigated as a routine, rapid, precise and selective analytical method for the determination of chromium(VI) in aqueous extracts of soil and sewage sludge. Chromatographic parameters were optimized for determination of Cr(VI), NO(-)(3) and SO(2-)(4). A low-capacity resin-based column was used for the separation and the anions were determined by conductometric detection. p-Hydroxybenzoic acid (5mM) at pH 8.5 was used as the eluent. The limit of detection, defined as S/N = 3, was 92 mug/l. The resolution between Cr(VI) and SO(2-)(4) was 2.8, the precision ranged from 0.9% for NO(-)(3) to 2.0% for Cr(VI) with a 500-mul injection. The SCIC results for Cr(VI) agreed closely with those obtained by inductively coupled argon-plasma emission and spectrophotometry. 相似文献
7.
K. Suvardhan K. Suresh Kumar D. Rekha K. Kiran B. Jaya Raj P. Chiranjeevi 《Journal of Analytical Chemistry》2007,62(4):336-341
Newly synthesized 2-propylpiperidine-1-carbodithioate (2-PPC) was used for the extraction of Cr(III), Ni(II), and Zn(II) from
various water samples. In the present investigation, the use of a syringe loaded with sorbent for the separation and enrichment
of Cr(III), Ni(II), and Zn(II) prior to their determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES)
was proposed to substitute the batch and column techniques. The described method was compared with the column technique with
respect to fastness, simplicity, recovery, and risk of contamination. The syringe was loaded with 1.0 g of sorbent in order
to retain the analyte elements. Next, 7.0 mL of sample solution (pH 5.0 ± 0.2) was drawn into the syringe in 15 s and discharged
over 15 s. Then, an eluent (3.0 M HCl) was drawn into the syringe and ejected back to desorb the analyte elements. At the
optimum conditions, the percentage recoveries of Cr(III), Ni(II), and Zn(II) were in the range of 94.50 to 99.62% with a standard
deviation (S.D.) of 0.03%. The elements could be concentrated by drawing and discharging several portions of sample successively
and eluting only one time. The detailed study of various interferences proved the method to be highly selective. The risk
of contamination is less than that with the column technique. The method was successfully applied to the determination of
Cr(III), Ni(II), and Zn(II) in spiked and natural water samples. The results obtained are in good agreement with those obtained
by the reported methods at the 95% confidence level.
The text was submitted by the authors in English. 相似文献
8.
KailasaSuresh Kumar Kanchi Suvardhan Dasari Rekha B. Jayaraj Pattium Chiranjeevi 《Helvetica chimica acta》2005,88(5):1022-1027
A facile, rapid, and sensitive spectrophotometric method for the determination of propoxur in insecticidal formulations, fortified water, vegetables, agricultural wastewater, and agricultural soil samples has been elaborated. The proposed method is based on the hydrolysis of propoxur under basic conditions, followed by instantaneous azo coupling of the resulting 2‐isopropoxyphenol with the anilines 2a – c . This yielded the orange‐red chromophore 3a (λmax=at 470 nm), the pale‐red coupling product 3b (490 nm), or the red derivative 3c (478 nm), which are stable for 46 h, 38 h, and 24 h, respectively, and could be readily analyzed spectrophotometrically. 相似文献
9.
Abdel-Magid AF Carson KG Harris BD Maryanoff CA Shah RD 《The Journal of organic chemistry》1996,61(11):3849-3862
Sodium triacetoxyborohydride is presented as a general reducing agent for the reductive amination of aldehydes and ketones. Procedures for using this mild and selective reagent have been developed for a wide variety of substrates. The scope of the reaction includes aliphatic acyclic and cyclic ketones, aliphatic and aromatic aldehydes, and primary and secondary amines including a variety of weakly basic and nonbasic amines. Limitations include reactions with aromatic and unsaturated ketones and some sterically hindered ketones and amines. 1,2-Dichloroethane (DCE) is the preferred reaction solvent, but reactions can also be carried out in tetrahydrofuran (THF) and occasionally in acetonitrile. Acetic acid may be used as catalyst with ketone reactions, but it is generally not needed with aldehydes. The procedure is carried out effectively in the presence of acid sensitive functional groups such as acetals and ketals; it can also be carried out in the presence of reducible functional groups such as C-C multiple bonds and cyano and nitro groups. Reactions are generally faster in DCE than in THF, and in both solvents, reactions are faster in the presence of AcOH. In comparison with other reductive amination procedures such as NaBH(3)CN/MeOH, borane-pyridine, and catalytic hydrogenation, NaBH(OAc)(3) gave consistently higher yields and fewer side products. In the reductive amination of some aldehydes with primary amines where dialkylation is a problem we adopted a stepwise procedure involving imine formation in MeOH followed by reduction with NaBH(4). 相似文献
10.
Sodium borohydride reduction of 3-methyl-2,3-dioxo-7,8-benzo-3-aza[3.3.3]propellan-6-one (1b) gave 2,4-dioxo-3-methyl-7,8-benzo-3-aza[3.3.3]propellan-6-ol, while lithium aluminum hydride reduction gave 3-methyl-7,8-benzo-3-aza[3.3.3]propellan-6-ol, which on oxidation, gave the corresponding ketone. This ketone formed the corresponding thioketal upon reaction with 1,2-ethanedithiol. Raney nickel desulfurization of the thioketal provided 3-methyl-6,7-benzo-3-aza[3.3.3]propellane. The same compound was also obtained in poor yield by forming the thioketal of Ib followed by lithium aluminum hydride reduction and Raney nickel desulfurization of the product. Desulfurization of the thioketal of Ib gave 2,4-dioxo-6,7-Benzo-3-aza[3.3.3]propellane. 相似文献