Simultaneous Determination of Pyridoxine Hydrochloride and Doxylamine Succinate from Tablets by Ion Pair Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC)

A new, simple, precise, and rapid ion pair reversed-phase high-performance liquid chromatography (RP-HPLC) method has been developed for the simultaneous determination of pyridoxine hydrochloride (PYR) and doxylamine succinate (DOX) in tablets. The stationary phase was a Microbondapak C18 column (10 μ, 300 mm × 3.9 mm i.d.). The mobile phase was water:methanol (60:40) containing 10 mM heptanesulfonic acid and 0.25% triethylamine and adjusted to pH 2.2 with orthophosphoric acid. Detection was carried out at 263 nm using an ultraviolet (UV) detector. The flow rate was 1.0 ml/min, and retention times were 3.65 min and 7.32 min for PYR and DOX, respectively. The linearity was obtained in the concentration range 0.5-500 μg/ml for PYR and DOX. Mean percentage recoveries were 100.20% and 101.20% for PYR and DOX, respectively.     

Complex permeability studies of Li1+ substituted Cu-Zn ferrites

Compositions having the general formula Zn_0.5Cu_0.5−tLi_2tFe₂O₄, where t=0.00, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, and 0.1, have been synthesized by using coprecipitation techniques using oxalate precursors. The initial permeability was calculated from the inductance measurements with a torroidal core of 100 turns, using the formula L=0.0046 μ_i N² h log d₂/d₁. There is a decrease in initial permeability (μ_i) with the substitution of Li¹⁺ ions which is explained on the Globus model. The values of rotational permeability (μ_rk) and μ_w have been calculated. In all the compositions, the main contribution to the initial permeability is due to domain wall motion. With addition of Li¹⁺ ions the wall permeability μ_w decreases, which suggest that these ions cause impedance to the domain wall motion. The frequency variation of μ′ and μ″ clearly indicate the low-frequency dispersion which may be attributed to the domain wall movements. From the L.F. studies it is concluded that the losses are minimum in the frequency region of 10 KHz to 1 MHz as expected for lithium ferrites.     

Designing a visualization framework for multidimensional data

Interest in visualization has grown in recent years, producing rapid advances in the diversity of research and in the scope of proposed techniques. Much of the initial focus in computer-based visualization concentrated on display algorithms, often for specific domains. For example, volume, flow, and terrain visualization techniques have generated significant insights into fundamental graphics and visualization theory, aiding the application experts who use these techniques to advance their own research. More recent work has extended visualization to abstract data sets like network intrusion detection, recommender systems, and database query results. This article describes our initial end-to-end system that starts with data management and continues through assisted visualization design, display, navigation, and user interaction. The purposes of this discussion are to (i) promote a more comprehensive visualization framework; (ii) describe how to apply expertise from human psychophysics, databases, rational logic, and artificial intelligence to visualization; and (iii) illustrate the benefits of a more complete framework using examples from our own experiences.     

Enzyme mass transfer coefficient in aqueous two phase system using a packed extraction column

Fractional dispersed phase hold-up and dispersed side mass transfer coefficients for amyloglucosidase were measured in a 56 mm i.d. packed extraction column using a sodium sulphate-polyethylene glycol 4000 system. Raschig rings (3 to 13.3 mm), Berl saddles (12 mm), Pall rings (12.6 mm), glass spheres (5.2 mm) and structured wire gauze were used as packings. The effect of packing size was investigated in the case of ceramic Raschig rings. The effect of phase composition of the aqueous phase system also was studied. Correlations have been developed for fractional dispersed phase hold-up and volumetric mass transfer coefficient with packing voidage, dry surface area of packings, superficial dispersed phase velocity and the liquid phase physical properties.     

Highly active three-dimensional cage type mesoporous ferrosilicate catalysts for the Friedel–Crafts alkylation

Three-dimensional cage type ferrosilicate catalysts with different n_Si/n_Fe ratios (FeSBA-1(x) where x denotes the n_Si/n_Fe molar ratio) have been prepared at a molar hydrochloric acid to silicon ratio of 10 using cetyltriethylammonium bromide as the template. The obtained materials have been unambiguously characterized by XRD, N₂ adsorption, and ESR spectroscopy, and their catalytic activity in the benzylation of benzene and the substituted benzene has also been investigated. The catalytic results of the FeSBA-1 catalysts with different n_Si/n_Fe ratios have been compared with the uni-dimensional FeSBA-15, AlSBA-15 and FeHMS catalysts. It has been found that the activity of the FeSBA-1 catalysts is much higher as compared to that of the FeSBA-15, FeHMS and AlSBA-15 catalysts. The activity of the catalysts declines in the following order: FeSBA-1(36) > FeSBA-1(90) > FeSBA-1(120) > FeSBA-1(344) > FeSBA-15(152) > FeHMS(50) > AlSBA-15(45). The effect of various reaction parameters such as reaction time, reaction temperature, reactant feed ratio and the various electron donating groups on the benzene ring affecting the activity and selectivity of FeSBA-1(344) have also been studied. The catalysts are highly active and show a complete conversion of benzyl chloride and a clean selectivity to diphenylmethane (DPM) within a short period of time under the optimized reaction conditions. The reaction kinetics of the catalysts has been extensively investigated and the results are presented. The apparent rate constant of the FeSBA-1(344) and the BC conversion sharply increase with increasing the reaction temperature. The activity of the FeSBA-1(344) catalyst for the benzylation of different aromatic compounds is in the following order: benzene > anisole > mesitylene > p-xylene > toluene.     

Kinetics of the formation of symmetrical wax esters from the corresponding alcohols with the use of hydrobromic acid and hydrogen peroxide

The primary aliphatic alcohols n-octanol, n-decanol, and n-dodecanol have been converted to their corresponding symmetrical esters by using HBr and H₂O₂ in the absence of a solvent. The reaction was carried out at 30, 40, and 50°C and at mole ratios of alcohol to HBr of 1∶0.1, 1∶0.2, 1∶0.3, and 1∶0.5. The rate of the reaction was found to increase with increase in the reaction temperature and concentration of HBr. The maximal conversion of n-octanol was 72% at 40°C and a mole ratio of n-octanol to HBr of 1∶0.5. The kinetics of the reaction have been established, and the reaction was found to be first-order with respect to alcohol and bromine concentration in the organic phase, and second-order with respect to both. The second-order rate constants for n-octanol, n-decanol, and n-dodecanol are 27.08, 32.58, and 37.42 mL mol⁻¹ min⁻¹, respectively, at 40°C. The activation energy for the esterification reaction of n-octanol was found to be 16.32 kcal mol⁻¹.     

Synthesis,characterization and photoluminescence properties of copper(II)–azido/thiocyanato complexes with thiazolylazo dye and1,2-bis(diphenylphosphino)ethane

A series of copper(II) complexes of the formula [Cu(L)(dppe)(N₃)₂] (1a–3a) and [Cu(L)(dppe)(NCS)₂] (1b–3b) (where L = 4-(2′-thiazolylazo)chlorobenzene (L₁); 4-(2′-thiazolylazo)bromobenzene (L₂) and 4-(2′-thiazolylazo)iodobenzene (L₃); dppe = cis-1,2-bis(diphenylphosphino)ethane) has been prepared and characterized on the basis of their elemental analysis, molar conductance, magnetic moment, IR, UV–vis and ¹H NMR spectral studies. The electrochemical behaviour of the complexes showed that the redox responses of copper(II) complexes shifted to more negative potential in order of decrease in electron withdrawing nature of the substituent on the azo ligands. All the complexes exhibit intraligand (π→π*) fluorescence in blue-green region with high quantum yield in DMF solution.     

The improved electromechanical sensitivity of polymer thin films containing carbon clusters produced in situ by irradiation with metal ions

Greatly enhanced electromechanical sensitivities were observed in ion beam irradiated polyimide films, where high resolution transmission electron microscopy and atomic force microscopy studies showed that 5.5 MeV Cu³⁺ ions produce randomly dispersed and highly oriented conducting nanochannels containing carbon clusters in polyimide with considerable overlap and narrow tunnel gap distributions between neighbouring nanochannels. Selected area electron diffraction studies confirmed the graphitic structure of these carbon clusters and also showed that the graphitic layers had preferential orientation parallel to the ion beam direction arising from relaxation of the graphitic layers within the nanochannels relieving local surface stresses in the polyimide matrix generated during irradiation as well as alignment of graphitic basal layers by volatile gases formed during irradiation escaping to the surface minimising resistance to gas flow. Electron energy loss spectroscopy also confirmed the graphitic structure of these carbon clusters within the nanochannels. Film electrical resistance increased exponentially with applied strain demonstrating the dominant role of tunnel gap modulation under strain. Gauge factors >1000 were achieved in these films at >3000 μstrains. Narrow distribution of tunnel gaps between the overlapping nanochannels is responsible for the high electromechanical sensitivities observed in these films compared to carbon nanotube–polymer (～50) films.