Indirect kinetic spectrophotometric determination of hydroxylamine based on its reaction with iodate.

A simple, precise and accurate method is proposed for rapid determination of trace amounts of hydroxylamine based on the reaction of hydroxylamine with iodate in acidic media. The reaction of neutral red by the produced nitrite ion was used to monitor the reaction spectrophotometrically at 525 nm by a fixed time method. Hydroxylamine in the range of 0.0400-1.200 microg mL(-1) could be determined. The relative standard deviation for 10 determinations of 0.500 microg mL(-1) hydroxylamine was 1.81% and the limit of detection was 0.010 microg mL(-1). The proposed method was applied to the determination of hydroxylamine in water samples with satisfactory results.     

Pentadiagonal Oscillatory Matrices with Two Spectrum in Common

We denote the spectrum of an square matrix A by σ(A), and that of the matrix obtained by deleting the first i rows and columns of A by σ_i(A). It is known that a symmetric pentadiagonal oscillatory (SPO) matrix may be constructed from σ, σ₁ and σ₂. The pairs σ, σ₁ and σ₁, σ₂ must interlace; the construction is not unique; and the conditions on the data which ensure that A is oscillatory are extremely complicated. Given one SPO matrix A, the paper shows that operations may be applied to A to construct a family of such matrices with σ and σ₁ in common. Moreover, given one totally positive (TP) matrix A, we construct a family of TP matrices with σ, σ₁ and σ₂ in common.     

Synthesis of New Dibenzosulfide and Dibenzosulfoxide Macrocyclic Compounds

Some new dibenzosulfo, dibenzosulfoxo macrocyclic diamides are synthesized.     

Spectrophotometric and AAS determination of trace amounts of cobalt after preconcentration by using alpha-benzilmonoxime-microcrystalline naphthalene.

The formed cobalt-a-benzilmonoxime complex was adsorbed onto microcrystalline naphthalene. Then it was determined by zero and first derivative spectrophotometry and by atomic absorption spectrophotometry (AAS) after dissolving into chloroform and methylisobutylketone (MIBK), respectively. Under optimum conditions, cobalt in the range of 1.0 - 20.0, 0.4 - 30.0 and 2.5 - 50.0 microg could be determined by spectrophotometry, first derivative spectrophotometry and AAS method, respectively. By the method, a preconcentration factor equal to approximately 30 for cobalt was obtained. The effect of diverse ions on the determination of 5.0 microg cobalt was also studied. The method was successfully applied to some pharmaceuticals and synthetic alloy samples.     

Simultaneous kinetic-spectrophotometric determination of hydrazine and acetylhydrazine in micellar media using the H-point standard addition method.

The H-point standard addition method (HPSAM), based on a spectrophotometric measurement for the simultaneous determination of hydrazine and acetylhydrazine, is described. This method is based on the difference between the rates of their reactions with N,N-dimethylaminobenzaldehyde (DAB) in the presence of sodium dodecyl sulfate (SDS) in acidic media. The results showed that hydrazine and acetylhydrazine could be determined simultaneously in the range of 0.020 - 0.70 and 0.20 - 5.0 mg L(-1), respectively. Under the working conditions, the proposed method was successfully applied to the simultaneous determination of hydrazine and acetylhydrazine in several synthetic mixtures and plasma and water samples.     

A Symmetric-Impulse Approximation Applied to the Faddeev Theory on the Charge Transfer Amplitude

Off-the-shell anomalous factors of the two-body Coulomb transition matrices appear in the integral form of the Faddeev second-order nuclear-electronic amplitude, for proton-hydrogen charge transfer scattering in a typical nlm → n′l′m′ transition. A symmetric-impulse approximation (SIA) is applied to eliminate these factors and an induction method is proposed to analytically calculate the remaining integrals. The nuclear-electronic amplitude is derived for the general case, and for totally symmetric collisions, in terms of generalized hypergeometric functions of two variables, F ₄, and of one variable, ₃ F ₂, respectively. The angular distribution of the second-order nuclear-electronic charge transfer amplitude shows the Thomas mechanism as a peak or a hump for symmetric and asymmetric collisions. There also exists a peak in the forward angular distribution of the second-order nuclear-electronic amplitude, which partly cancels the kinematic peak in the angular distribution of the charge transfer differential cross sections.     

Syntheses of 5‐alkylthio‐1,3‐diaryl‐1,2,4‐triazoles

Arylation of the readily available 3‐alkythio‐5‐aryl‐1,2,4‐triazoles gave 5‐alkylthio‐1,3‐diaryl‐1,2,4‐triazoles in moderate yield. The structures of the latter were confirmed by NOE and ¹³C‐NMR.     

Hyers-Ulam-Rassias stability of homomorphisms in quasi-Banach algebras associated to the Pexiderized Cauchy functional equation

In this paper, we prove the Hyers-Ulam-Rassias stability of homomorphisms in quasi-Banach algebras associated to the Pexiderized Cauchy functional equation. This is applied to investigate homomorphisms between quasi-Banach algebras. The concept of Hyers-Ulam-Rassias stability originated from Th.M. Rassias' stability theorem that appeared in his paper [Th.M. Rassias, On the stability of the linear mapping in Banach spaces, Proc. Amer. Math. Soc. 72 (1978) 297-300].