Relative efficiencies of substituted aromatic monocarboxylic acids as eluents in ion chromatographic separation of inorganic and organic anions

The eluent strengths of para, ortho and meta substituted hydroxy-, nitro-, amino- and sulfobenzoic acids in single column ion chromatographic separations of inorganic and organic anions have been evaluated and compared with benzoic acid.o-Sulfobenzoic acid turns out to be a stronger and efficient eluent compared to others for the separation and determination of monovalent (Cl^–, NO ₂ ^– , Br^–, NO ₃ ^– ) and divalent (SO ₄ ^2– , SeO ₄ ^2– , S₂O ₃ ^2– , S₂O ₆ ^2– ) inorganic anions. In addition it also functions as an appropriate mobile phase for the detection and quantification of some substituted benzoate ions in an aqueous medium.     

Analytical applications of mercaptan-carbon disulphide reaction: Determination of mixtures containing mercaptans

Summary A method is described for the determination of mercaptans by alkalimetric titration of trithiocarbonic acids formed through their reaction with carbon disulphide in tert.-butanol. The method has been applied to the analysis, on the same sample solution, of mixtures of mercaptans containing titrable hydrogen and those containing nontitrable hydrogen, mercaptans and alkali mercaptides, and mercaptans and mercaptopyrimidines.

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Analytische Anwendung der Merkaptan-Schwefelkohlenstoff-Reaktion: Bestimmung von Merkaptan in Gemischen

Zusammenfassung Ein Verfahren zur Merkaptanbestimmung durch alkalimetrische Titration der Trithiokohlensäure auf der Grundlage seiner Reaktion mit Schwefelkohlenstoff in tert. Butanol wurde beschrieben. Es eignet sich zur Bestimmung von Gemischen aus Merkaptanen mit titrierbarem Wasserstoff und solchen ohne titrierbaren Wasserstoff sowie von Merkaptanen und Merkaptiden, weiters von Merkaptanen und Merkaptopyrimidinen.

     

Dual control mechanism in a Belousov-Zhabotinskii (B-Z) oscillator with glucose and oxalic acid as a double substrate

Oscillations in a Belousov-Zhabotinskii (B-Z) system having oxalic acid (OA) and glucose (G) as a mixed organic substrate, neither of which acts as a bromine scavenger, have been investigated. Studies have been performed for (i) varying the concentration of G while keeping the OA concentration fixed and (ii) varying OA but keeping G fixed in a batch reactor. In both cases upper and lower critical limits occur, between which oscillations are observed. Both single and double frequency oscillations have been observed in a wide range of concentrations of G as well as of OA. The induction period in most of the cases was <1 min. When G is fixed and OA is varied, the time pause between the sequential oscillations increases with an increase in OA. On the other hand when OA is fixed and G is varied, the time-pause decreases with an increase in G. The first type of oscillation is Br(-)-controlled, whereas the second is non-Br(-)-controlled. The order of addition of G and OA in the last has no influence on the induction period. It influences, however, the oscillatory characteristics. Br(2) evolution in the G + OA + Ce(4+) + BrO(3)(-) + H(2)SO(4) reaction system has been investigated spectrophotometrically. ESR and polymerization studies indicate the important role of free radicals in influencing the reaction mechanism. A tentative dual control mechanism has been suggested involving autocatalysis of HBrO(2) and BrO2*.     

Generalization of five q-series identities of Ramanujan and unexplored weighted partition identities

The Ramanujan Journal - Ramanujan recorded five interesting q-series identities in a section that is not as systematically arranged as the other chapters of his second notebook. These five...     

Fabrication and characterization of ‘self-binding’ nanocrystalline SnO2 powder based thick film ethanol sensor

Sensing response of ‘self-binding’ nanoparticles of tin dioxide powder deposited on alumina substrate has been investigated. The nanocrystalline SnO₂ powder has been derived from stannic chloride. It has been prepared through fine crystallization in liquid phase. SnO₂ powder has been characterized using SEM, TEM and XRD techniques, which reveal that the average crystallite size is of 12 nm. The slurry blobs deposited on alumina substrate of the powder-thus-prepared have been studied for sensing response to ethanol at various temperatures and concentrations. The observations reveal that the material prepared is ‘self-binding’ and is very sensitive even without catalyst.     

Effect of injecting electrodes on TSD behaviour of vacuum deposited PVF films

Depolarization behaviour of vacuum deposited polyvinyl fluoride (PVF) films has been studied as a function of nature of the electrode materials used during polarization such as copper, silver, aluminium and indium using the thermally stimulated discharge current (TSD) technique. TSD spectra of these films show a single relaxation peak centered around 430 ± 1 K with activation energies of ∼ 0.65 eV. The peak current and the charge associated with the relaxation peak depend strongly on the electrode material used. This has been attributed to the electrode-polymer interface barrier controlling the injection of the charge carriers into PVF films that results into space charge effects by subsequent trapping of the injected charge carriers at macroscopic distances. Paper presented at the 2nd International Conference on Ionic Devices, Anna University, Chennai, India, Nov. 28–30, 2003.     

Role of polyvinyl alcohol in the conductivity behaviour of polyethylene glycol-based composite gel electrolytes

An attempt has been made in the present work to combine gel and composite polymer electrolyte routes together to form a composite polymeric gel electrolyte that is expected to possess high ionic conductivity with good mechanical integrity. Polyethylene glycol (PEG) based composite gel electrolytes using polyvinyl alcohol (PVA) as guest polymer have been synthesized with 1 molar solution of ammonium thiocyanate (NH₄SCN) in dimethyl sulphoxide (DMSO) and electrically characterized. The ionic conductivity measurements indicate that PEG:PVA:NH₄SCN-based composite gel electrolytes are superior (σ _max = 5.7 × 10⁻² S cm⁻¹) to pristine electrolytes (PEG:NH₄SCN system) and conductivity variation with filler concentration remains within an order of magnitude. The observed conductivity maxima have been correlated to PEG:PVA:NH₄SCN-and PVA:NH₄SCN-type complexes. Temperature dependence of conductivity profiles exhibits Arrhenius behaviour in low temperature regime followed by VTF character at higher temperature.      

J/psi production from proton-proton collisions at square root of s=200 GeV

J/psi production has been measured in proton-proton collisions at square root of s=200 GeV over a wide rapidity and transverse momentum range by the PHENIX experiment at the Relativistic Heavy Ion Collider. Distributions of the rapidity and transverse momentum, along with measurements of the mean transverse momentum and total production cross section are presented and compared to available theoretical calculations. The total J/psi cross section is 4.0+/-0.6(stat)+/-0.6(syst)+/-0.4(abs) mu b. The mean transverse momentum is 1.80+/-0.23(stat)+/-0.16(syst) GeV/c.     

Absence of suppression in particle production at large transverse momentum in sqrt[s(NN)]=200 GeV d+Au collisions

Transverse momentum spectra of charged hadrons with p(T)<8 GeV/c and neutral pions with p(T)<10 GeV/c have been measured at midrapidity by the PHENIX experiment at BNL RHIC in d+Au collisions at sqrt[s(NN)]=200 GeV. The measured yields are compared to those in p+p collisions at the same sqrt[s(NN)] scaled up by the number of underlying nucleon-nucleon collisions in d+Au. The yield ratio does not show the suppression observed in central Au+Au collisions at RHIC. Instead, there is a small enhancement in the yield of high momentum particles.     

Suppressed pi(0) production at large transverse momentum in central Au+Au collisions at sqrt[s(NN)]=200 GeV

Transverse momentum spectra of neutral pions in the range 1相似文献