Some necessary and sufficient conditions for Hypercyclicity Criterion

We give necessary and sufficient conditions for an operator on a separable Hilbert space to satisfy the hypercyclicity criterion. This paper is a part of the second author’s Doctoral thesis, written at Shiraz University under the direction of the first author.     

Synthesis of New Dibenzosulfide and Dibenzosulfoxide Macrocyclic Compounds

Some new dibenzosulfo, dibenzosulfoxo macrocyclic diamides are synthesized.     

On the nonlinear distortion of subcarrier multiplexed systems owing to stimulated Brillouin scattering

Analytical expressions are obtained for predicting the harmonic and intermodulation performance of subcarrier multiplexed systems owing to stimulated Brilloun scattering. These expressions are in terms of the ordinary Bessel functions with arguments depenedent on the modulation index.     

Large signal performance of micromachined silicon inductive microphones

A mathematical model for the open-circuit output voltage of a micromachined silicon inductive microphone is presented. The model, basically a sine-series function, can easily yield closed-form expressions for the amplitudes of the output components resulting from a multisinusoidal input acoustic pressure. The special case of an equal-amplitude two-tone acoustic pressure input is considered in detail. The results show that, the microphone generates both even and odd-order harmonic and intermodulation products.     

Empirical model for the current-voltage characteristic of resonant-tunneling devices

An empirical model is presented for the current-voltage characteristics of resonanttunneling (RT) devices. By using this model an analytical study of millimeter-band electronic circuits employing RT devices can be performed.     

Solid-liquid extraction and preconcentration of trace nickel using 2-nitroso-1-naphthol-4-sulfonic acid (Nitroso-S) and TDBA onto benzophenone and determination by atomic absorption spectrometry.

Nickel was quantitatively retained by 2-nitroso-1-naphthol-4-sulfonic acid (Nitroso-S) and tetradecyldimethylbenzylammonium chloride (TDBA Cl) onto benzophenone in the pH range 5.0-6.0 from large volumes of aqueous solutions of various samples. After filtration, each solid mass consisting of a nickel complex and benzophenone was dissolved with 5 ml of dimethylformamide (DMF) and the metal was determined by atomic absorption spectrometry (AAS). About 0.6 microg of nickel could be concentrated from 200 ml of an aqueous sample, where its concentration was as low as 3.0 ng/ml. Eight replicate determinations of 2.5 microg/ml of nickel in the final DMF solution gave a mean absorbance of 0.112 with a relative standard deviation of 1.9%. The sensitivity for 1% absorption was 98 ng/ml. The interference of a number of anions and cations was studied and the developed optimized conditions were utilized for the trace determination of nickel in various alloys and biological samples.     

Harmonic and intermodulation generation in quantum-well diodes

A Fourier-series model describing the current-voltage characteristic of a quantum-well diode (QWD) is presented. Using this model, closed-form expressions are obtained for the harmonic and intermodulation performance of a QWD excited by a multisinusoidal voltage superimposed on a dc voltage.     

Highly selective thiocyanate poly(vinyl chloride) membrane electrode based on a cadmium-Schiff's base complex

A PVC membrane electrode based on a cadmium-salen (N,N'-bis-salicylidene-1,2-ethylenediamine) complex as an anion carrier is described. The electrode has an anti-Hofmeister selectivity sequence with a preference for thiocyanate at pH 1.5-11.0. It has a linear response to thiocyanate from 1.0 x 10(-6) to 1.0 x 10(-1) mol L(-1) with a slope of 59.1 +/- 0.2 mV per decade, and a detection limit of 7 x 10(-7) mol L(-1). This electrode has high selectivity for thiocyanate relative to many common organic and inorganic anions. The proposed sensor has a fast response time of approximately 15 s. It was applied to the determination of thiocyanate in a milk sample.     

Differential Pulse Polarographic Determination of Trace Amounts of Lead in Alloys and Biological Samples after Column Preconcentration Using Nitroso-S and TDBA

A highly selective, sensitive, rapid, and economical differential pulse polarographic method has been developed for the determination of trace amounts of lead in various standard alloys and biological samples after the adsorption of its 2-nitroso-l-naphthol-4-sulfonic acid (nitroso-S)—tetradecyldimethylbenzylammonium (TDBA) chloride on microcrystalline naphthalene in the pH range of 8.0–10.5. After filtration, the solid mass is shaken with 9.0 mL of 1 M hydrochloric acid, and lead is determined by differential pulse polarography (DPP). Lead can alternatively be quantitatively adsorbed on 2-nitroso-l-naphthol-4-sulfonic acid-tetradecyldimethylbenzylammonium-naphthalene adsorbent packed in a column and determined similarly. In this case, 1.0 g of lead can be concentrated in a column from 500 mL of an aqueous sample in which its concentration is as low as 2 ng/mL. Characterization of the electroactive process included an examination of the degree of reversibility. Various parameters, such as the pH effect, volume of aqueous phase, HCl concentration, reagent concentration, naphthalene concentration, shaking time, and the interference of a number of metal ions on the determination of lead were studied in detail to optimize the conditions for determination in standard alloys and standard biological samples.     

Column preconcentration of trace manganese with the ion pair of 2-nitroso-1-naphthol-4-sulfonic acid tetradecyldimethylbenzyl-ammonium chloride supported on naphthalene and determination by derivative spectrophotometry

A column preconcentration method has been developed for the determination of trace amounts of manganese by preconcentration on 2-nitroso-1-naphthol-4-sulfonic acid (nitroso-S)-tetradecyldimethylbenzylammonium (TDBA) naphthalene as an adsorbent using a simple funnel tipped glass tube. Manganese reacts with nitroso-S to form a water soluble brown colored chelate anion. The chelate anion forms a water insoluble Mn-Nitroso-S-TDBA ion pair on naphthalene packed in a column in the pH range 9.6-10.5 at a flow rate of 1-2 ml/min. The solid mass consisting of manganese complex and naphthalene is dissolved in 5 ml of dimethylformamide (DMF) and the metal determined by second derivative spectrophotometry. The calibration curve is linear in the concentration range 0.25-35.0 micrograms of Mn in 5 ml of the final DMF solution. Eight replicate determinations of 25 micrograms of standard manganese solution give a mean peak height of 4.0 with a correlation coefficient of 0.9995 and relative standard deviation of +/- 1.1%. The sensitivity was calculated to be 0.502(d2 A/d lambda 2)/microgram ml-1 from the slope of the calibration curve. The detection limit was 0.020 microgram ml-1 for manganese at the minimum instrumental settings (signal to noise ratio = 2). Various parameters effecting the method such as the effect of pH, volume of aqueous phase and interference of a number of metal ions on the determination of manganese have been evaluated to optimize the conditions for its determination in standard alloys and biological samples.