Concept of multipole magnetic field rotation in ECRIS

The conventional type of magnetic well is formed by superposition of two types of magnetic field, axial bumpy field and radial multipole field. It is used to contain plasma that consists of neutrals, ions and electrons. These particles are in constant motion in the well and energetic electrons create plasma by violent collisions with neutrals and ions. The confined electrons are constantly heated by ECR technique in the presence of magnetic field. In this paper it has been shown theoretically that how the electron motion is influenced in terms of heating, containment and azimuthal uniformity of plasma, by the axial rotation of the multipole magnetic field [1,2]. Afterwards, the feasibility of achieving a rotating magnetic multipole field is discussed to some extent. And it is seen that it is not beyond the capability of the scientific community in the present scenario of the advanced technology. Presently, it can be achieved for lesser field and slightly larger size of the multipole electromagnet and can be used for improvement of the ECR ion source (ECRIS).     

The analysis of alkyl-capped alcohol ethoxylates and alcohol ethoxycarboxylates from alcohol ethoxylates by atmospheric pressure chemical ionization mass spectrometry

Alcohol ethoxylates (AEs) are nonionic surfactants. They are industrially important compounds that have historically been difficult to analyze, with the best results to date achieved through derivatization (e.g., silylation) followed by analysis by gas chromatography/mass spectrometry (GC/MS). Recently, mass spectrometric techniques such as field desorption (FD), time-of-flight secondary ion mass spectrometry (TOF-SIMS), fast atom bombardment (FAB), electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI) have been employed to analyze surfynol(R) 4xx. In an effort to produce low-cost alkyl-capped AEs and anionic detergents from AEs, a fast and reliable measure of the product yields and conversions from AEs is required in research. We found that the product yields and conversions from reactions of AEs, obtained by the employment of atmospheric pressure chemical ionization (APCI), were in good agreement with those obtained from proton nuclear magnetic resonance spectroscopy ((1)H-NMR). Therefore, APCI can be used as a validated tool for studying AE reactions. Mixtures that contain either silylated or unsilylated ethoxylates and/or carboxylates yield the same APCI mass spectra. Copyright -Copyright 1999 John Wiley & Sons, Ltd.     

Poly(arylene sulfide)s via nucleophilic aromatic substitution reactions of halogenated pyromellitic diimides

Nucleophilic aromatic substitution (SNAr) reactions are exploited to prepare poly(arylene sulfide)s (PAS's) via the reaction of bis-thiolates and dibrominated pyromellitic diimide (PMDI) derivatives. Small-molecule model studies reveal the reaction is well-defined and proceeds in quantitative yield in practical times at room temperature. Variation in comonomer feed ratios allowed some control over target polymer molecular weights in the step polymerization, but control was likely limited by the relatively poor polymer solubility in the dipolar aprotic solvents typically employed to promote SNAr reactions. One substitution pattern produces a steric “pocket” around the PMDI units, inducing a peculiar solubility trend in halogenated solvents; that is, greatly reduced solubility in CHCl₃ relative to CH₂Cl₂ and C₂H₂Cl₄. One example small-molecule readily dissolves in CHCl₃ at room temperature, then rapidly grows poorly soluble crystals revealed by single-crystal XRD to contain CHCl₃ molecules in the steric pockets. Finally, the recently demonstrated depolymerization of phthalonitrile-based PAS's via ipso substitution with monothiolates as chain scission agents yields quantitative molecular weight reduction to monomeric species from the polymers reported here.     

Application of Flying Jet Plasma for Production of Biodiesel Fuel from Wasted Vegetable Oil

Biodiesel, a good partial or total substitute for petrodiesel, is a renewable clean burning fuel which can be produced from transesterification of vegetable oils and animal fats with an alcohol in presence of a catalyst. Since the feedstock costs in this process constitutes more than 70 % of the overall cost, use of wasted vegetable oil (i.e. consumed cooking oil) for biodiesel production is a big challenge in terms of cost reduction and environmental impacts. Nonetheless, the content of residues in the wasted vegetable oil, formed during frying, is a major drawback could be faced in this direction. In this research, we applied an unconventional design of flying jet dielectric barrier discharge plasma torch to treat several specimens of wasted cooking oil collected from different resources before transesterification. In other experiments, the jet plasma itself was used to catalyze the reaction process. The examined plasma torch was found more feasible than conventional DBD reactor design in terms of gas and power consumptions. Upon inducting plasma treatment, the transesterification process resulted in higher biodiesel yield, lower reaction time and easier product separation than the conventional path. Upon catalyzing the reaction by the sole jet plasma effect, the biodiesel content of saturated methyl esters was higher than conventional tranesterification. Also, the yield and properties were found within commercial standards.     

Fuzzy closure spaces

Fuzzy topological spaces do not constitute a natural boundary for the validity of theorems, but many results can be extended to what are called fuzzy closure spaces (or fcs's, for short). The notions of a subspace, a sum, and a product are extended to fcs's. The hereditary, additivity, and productivity behaviour of compactness in fcs's is investigated and some weak forms of compactness and fuzzy continuous functions in fcs's are introduced. The interaction between fuzzy proximity spaces and fcs's is investigated; A necessary background is included for completeness.     

A novel method for the synthesis of 1-aryltetrahydroisoquinolines

Carbenium ions generated from substituted benzhydryls using acid catalysis undergo smooth intramolecular trapping by pendant sulfonamide groups to provide excellent yields of 1-aryltetrahydroisoquinolines.     

Features of Triaxial Superdeformed Bands in Odd Mass Nuclei Using the Cranked Nilsson–Strutinsky Model

Physics of Atomic Nuclei - The axial asymmetry deformation parameter $$\gamma$$ , the gamma transition energies, rotational frequencies, kinematic and dynamic moments of inertia in triaxial...     

Aloeverasides A and B: Two Bioactive C‐Glucosyl Chromones from Aloe vera Resin

Two new C‐glucosyl chromones named aloeverasides A ( 1 ) and B ( 2 ) were isolated from the resin of Aloe vera (L.) Burm.f . The structures of the two new natural products were elucidated based on 1D‐ (¹H‐ and ¹³C‐NMR) and 2D‐NMR (COSY, HSQC, and HMBC) spectroscopic techniques and mass spectrometry (ESI‐MS). Aloeverasides A ( 1 ) and B ( 2 ) were evaluated for their anticancer activity, and both induced a 76.4 and 70.5% growth inhibition of the breast cancer cell line (MDA‐MB‐231) at a concentration of 100 μm . Both compounds were also evaluated for their 1,1‐diphenyl‐2‐picryl‐hydrazyl antioxidant, urease enzyme, and α‐glucosidase enzyme inhibition activities. Aloeverasides A ( 1 ) and B ( 2 ) displayed good urease enzyme inhibition activities (62 and 55%, resp.), as well as antioxidant activity in which aloeveraside A ( 1 ) had a value of 60% inhibition, while aloeveraside B ( 2 ) demonstrated a more potent antioxidant activity with 80% inhibition.