Polypyrrole–montmorillonite nanocomposite as sorbent for solid‐phase microextraction of phenolic compounds in water

A fiber‐coated polypyrrole–montmorillonite nanocomposite was prepared for solid‐phase microextraction. The fiber coating can be prepared easily; it is mechanically stable and exhibits relatively high thermal stability. The prepared fiber was evaluated for the extraction of some phenolic compounds from aqueous sample solutions by gas chromatography–mass spectrometry. The effects of the extraction and desorption parameters including extraction time, extraction temperature, stirring rate, ionic strength, pH and desorption temperature and time have been studied. At optimum conditions, the repeatability for one fiber (n = 5), expressed as % relative standard deviation was between 6.5 and 7.8% for the phenolic compounds. The detection limits for the studied phenolic compounds were between 0.05–1.3 ng/mL. The developed method offers the advantage of being simple to use, with shorter analysis time, lower cost, thermal stability of the fibers, and high relative recovery in comparison to conventional methods of analysis.     

Polyol‐enhanced dispersive liquid–liquid microextraction coupled with gas chromatography and nitrogen phosphorous detection for the determination of organophosphorus pesticides from aqueous samples,fruit juices,and vegetables

Polyol‐enhanced dispersive liquid–liquid microextraction has been proposed for the extraction and preconcentration of some organophosphorus pesticides from different samples. In the present study, a high volume of an aqueous phase containing a polyol (sorbitol) is prepared and then a disperser solvent along with an extraction solvent is rapidly injected into it. Sorbitol showed the best results and it was more effective on the extraction recoveries of the analytes than inorganic salts such as sodium chloride, potassium chloride, and sodium sulfate. Under the optimum extraction conditions, the method showed low limits of detection and quantification within the ranges of 12–56 and 44–162 pg/mL, respectively. Enrichment factors and extraction recoveries were in the ranges of 2799–3033 and 84–92%, respectively. The method precision was evaluated at a concentration of 10 ng/mL of each analyte, and relative standard deviations were found to be less than 5.9% for intraday (n = 6) and less than 7.8% for interday (n = 4). Finally, some aqueous samples were successfully analyzed using the proposed method and four analytes (diazinon, dimethoate, chlorpyrifos, and phosalone) were determined, some of them at ng/mL level.     

On the existence of chaotic circumferential waves in spinning disks

We use a third-order perturbation theory and Melnikov's method to prove the existence of chaos in spinning circular disks subject to a lateral point load. We show that the emergence of transverse homoclinic and heteroclinic points lead, respectively, to a random reversal in the traveling direction of circumferential waves and a random phase shift of magnitude pi for both forward and backward wave components. These long-term phenomena occur in imperfect low-speed disks sufficiently far from fundamental resonances.     

Headspace SPME–GC Method for Acetone Analysis and its Biomedical Application

A new method for extraction and analysis of acetone in human urine based on headspace solid phase microextraction using a mixture of activated carbon and zeolite as sorbents in a PVC matrix coated on a silver wire and its application to the determination of ketone bodies is described. Unlike commercial fibers, which are coated on fused silica, the coating adheres strongly to the silver wire and is thermally stable up to 250 °C. After optimization of coating composition and microextraction conditions the fiber was used for the analysis of acetone in human urine.     

Theoretical Treatment of a Cathodic Stripping Mechanism of an Insoluble Salt Coupled with a Chemical Reaction in Conditions of Square Wave Voltammetry. Application to 6‐Mercaptopurine‐9‐D‐Riboside in the Presence of Ni(II)

Cathodic stripping mechanism of an insoluble salt coupled with a homogenous chemical reaction is considered both theoretically and experimentally under conditions of square‐wave voltammetry. For the mercury electrode in aqueous solution, the electrode reaction is described as L(aq)+Hg(l)=HgL(s)+2e^?, where L(aq) is the reactive ligand that forms a sparingly soluble compound HgL(s). The electrode reaction is coupled with a homogenous, first‐order chemical reaction, A(aq)=L(aq). Theoretical predictions are confirmed by experiments with 6‐mercaptopurine‐9‐D‐riboside in the presence of nickel(II) ions.     

Search for lepton flavor violation in the decay tau+/- --> mu+ gamma

A search for the nonconservation of lepton flavor number in the decay tau(+/-) --> mu(+/-) has been performed using 2.07 x 10(8) e(+ )e(-) tau(+) tau(-) events produced at a center-of-mass energy near 10.58 GeV with the BABAR detector at the PEP-II storage ring. We find no evidence for a signal and set an upper limit on the branching ratio of Beta(tau(+/-) --> mu(+/-) gamma) < 6.8 x 10(-8) at 90% confidence level.     

On ideals with the Rees property

A homogeneous ideal I of a polynomial ring S is said to have the Rees property if, for any homogeneous ideal ${J \subset S}$ which contains I, the number of generators of J is smaller than or equal to that of I. A homogeneous ideal ${I \subset S}$ is said to be ${\mathfrak{m}}$ -full if ${\mathfrak{m}I:y=I}$ for some ${y \in \mathfrak{m}}$ , where ${\mathfrak{m}}$ is the graded maximal ideal of ${S}$ . It was proved by one of the authors that ${\mathfrak{m}}$ -full ideals have the Rees property and that the converse holds in a polynomial ring with two variables. In this note, we give examples of ideals which have the Rees property but are not ${\mathfrak{m}}$ -full in a polynomial ring with more than two variables. To prove this result, we also show that every Artinian monomial almost complete intersection in three variables has the Sperner property.     

Energetic Silver Salts with 5-Aminotetrazole Ligands

Methylation of 5-amino-1H-tetrazole ( 1 ) gives 1-methyl-5-amino-1H-tetrazole ( 2 ) and 2-methyl-5-amino-1H-tetrazole ( 3 ). A new family of energetic silver complexes based on ligands 1 , 2 and 3 with perchlorate and nitrate anions ( 10 – 15 ) were synthesized and characterized by using IR, Raman, and NMR (¹H, ¹³C, ¹⁴N, and ³⁵Cl NMR) spectroscopy, elemental analysis, and mass spectrometry. The crystal structures of the compounds were determined where possible and reveal interesting structural details that are discussed herein. Additionally, differential scanning calorimetry was used to assess the thermal stability of the new salts, which showed excellent thermal stabilities at temperatures up to and above 225 °C. Standard tests were also used to assess the sensitivity of the materials towards impact and friction. All the silver complexes showed increased sensitivity values in comparison with analogous protonated 5-amino-1H-tetrazolium perchlorate and nitrate salts. Some of these materials have sensitivity values that are comparable to commonly used primary explosives and all of them either deflagrate ( 12 – 14 ) or detonate loudly ( 10 and 11 ) on contact with an open flame. Lastly, nitrate salt 11 is easily initiated by thermal shock. It shows reasonably low sensitivity in comparison with other silver salts (e.g., silver azide or silver fulminate), which makes handling it much less hazardous. Compound 11 also has good thermal stability, decomposing at ≈300 °C, and shows interesting properties as a more environmentally benign alternative to lead(II) diazide in initiation devices for civil and military applications.     

Gas chromatographic technique for determination of Irgafos 168 in polyolefin samples after conversion to the related phenolic compound by saponification

A gas chromatographic technique is reported for the determination of a secondary antioxidant, Irgafos 168, in polymeric samples. Irgafos 168 [tris(2,4-di-tert-butyl phenyl)phosphite] is extracted by dissolution/precipitation, saponified to 2,4-di-tert-butyl phenol by refluxing in the presence of methanolic potassium hydroxide, and determined by gas chromatography-flame ionization detection. The method’s repeatability is good, and the relative standard deviation is 7.5% (between runs) and 15.5% (between days). This method was applied to the determination of Irgafos 168 in commercial polymers, and the obtained results were in relatively good agreement with those obtained by the previously reported spectrophotometric method. Correspondence: Mir Ali Farajzadeh, Department of Chemistry, Faculty of Science, Urmia University, Urmia, Iran