Simple and sensitive spectrophotometric method for determination of tricyclic antidepressant imipramine using Fe(III)-SCN<Superscript>−</Superscript> complex

A new simple procedure for the spectrophotometric determination of tricyclic antidepressant drug imipramine is proposed. The method is based on the enhancement of the colour intensity of the Fe(III)-SCN⁻ complex due to the addition of the drug imipramine. The value of molar absorptivity of the Fe(III)-SCN⁻ imipramine complex in terms of the drug lies in the range of (2.77–3.16) × 10³ L/mol cm at the absorption maximum 460 nm. The detection limit of the method was 250 μg/L. The slope, intercept, and correlation co-efficient for the present method were found to be 0.008, 0.005, and 0.998, respectively. The effect of analytical variables on the determination of the drug and the composition of the complex are discussed. The method is applicable to the determination of imipramine in the drug samples.     

Observation and polarization measurements of B+/- -->phiK1 +/- and B +/- -->phiK2 *+/-

With the full BABAR data sample of 465 x 10(6) B(over)B pairs, we observe the decays B+/- -->phiK_(1)(1270) +/- and B +/- -->phiK*_(2)(1430)+/-. We measure the branching fractions (6.1+/-1.6+/-1.1) x 10(-6) and (8.4+/-1.8+/-1.0) x 10(-6) and the fractions of longitudinal polarization 0.46 (+0.12+0.06) _(-0.13-0.07) and 0.80(+0.09)_(-0.10)+/-0.03, respectively. We also report on the B+/- -->phiK*_(0)(1430)+/- decay branching fraction of (7.0+/-1.3+/-0.9) x 10(-6) and several parameters sensitive to CP violation and interference in the above three decays. Upper limits are placed on the B+/- decay rates to final states with phi and K_1(1400)+/-, K*(1410)+/-, K2(1770)+/-, or K_2(1820)+/-. Understanding the observed polarization pattern requires amplitude contributions from an uncertain source.     

Measurements of B --> {pi,eta,eta;{'}}lnu_{l} branching fractions and determination of |V_{ub}| with semileptonically tagged B mesons

We report measurements of branching fractions for the decays B-->Plnu_{l}, where P are the pseudoscalar charmless mesons pi;{-}, pi;{0}, eta and eta;{'}, based on 348 fb;{-1} of data collected with the BABAR detector, using B0 and B+ mesons found in the recoil of a second B meson decaying as B-->D;{(*)}lnu_{l}. Assuming isospin symmetry, we combine pionic branching fractions to obtain B(B;{0}-->pi;{-}l;{+}nu_{l})=(1.54+/-0.17_{(stat)}+/-0.09_{(syst)})x10;{-4}; we find 3.2sigma evidence of the decay B;{+}-->etal;{+}nu_{l} and measure its branching fraction to be (0.64+/-0.20_{(stat)}+/-0.03_{(syst)})x10;{-4}, and determine B(B;{+}-->eta;{'}l;{+}nu_{l})<0.47x10;{-4} to 90% confidence level. Using partial branching fractions for the pionic decays in ranges of the momentum transfer and a variety of form factor calculation, we obtain values of the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element |V_{ub}| in ranging from 3.6x10;{-3} to 4.1x10;{-3}.     

Synthesis of composite gold/tin-oxide nanoparticles by nano-soldering

Composite Au–SnO₂ nanoparticles (NPs) are synthesized by nano-soldering of pure Au and SnO₂ NPs. The multi-step process involves synthesis of pure Au and SnO₂ NPs separately by nanosecond pulse laser ablation of pure gold and pure tin targets in deionized water and post-ablation laser heating of mixed solution of Au colloidal and SnO₂ colloidal to form nanocomposite. Transmission Electron Microscopy (TEM) and High-Resolution Transmission Electron Microscopy (HRTEM) were used to study the effect of laser irradiation time on morphology of the composite Au–SnO₂ NPs. The spherical particles of 4 nm mean size were obtained for 5 min of post-laser heating. Increased mean size and elongated particles were observed on further laser heating. UV–vis spectra of Au–SnO₂ nanocomposites show red shift in the plasmon resonance absorption peak and line shape broadening with respect to pure Au NPs. The negative binding energy shift of Au 4f_7/2 peak observed in X-ray Photoelectron Spectra (XPS) indicates charge transfer in the nano-soldered Au–SnO₂ between gold and tin oxide and formation of soldered nanocomposite.     

$$Q\bar{Q}$$ ($$Q\in \{b,c\}$$Q∈{b,c}) spectroscopy using the Cornell potential

The mass spectra and decay properties of heavy quarkonia are computed in nonrelativistic quark-antiquark Cornell potential model. We have employed the numerical solution of Schrödinger equation to obtain their mass spectra using only four parameters namely quark mass (\(m_c\), \(m_b\)) and confinement strength (\(A_{c\bar{c}}\), \(A_{b\bar{b}}\)). The spin hyperfine, spin-orbit and tensor components of the one gluon exchange interaction are computed perturbatively to determine the mass spectra of excited S, P, D and F states. Digamma, digluon and dilepton decays of these mesons are computed using the model parameters and numerical wave functions. The predicted spectroscopy and decay properties for quarkonia are found to be consistent with available data from experiments, lattice QCD and other theoretical approaches. We also compute mass spectra and life time of the \(B_c\) meson without additional parameters. The computed electromagnetic transition widths of heavy quarkonia and \(B_c\) mesons are in tune with available experimental data and other theoretical approaches.     

Coagulation Behavior of Antimony Oxyanions in Water: Influence of pH,Inorganic and Organic Matter on the Physicochemical Characteristics of Iron Precipitates

The presence of inorganic and organic substances may alter the physicochemical properties of iron (Fe) salt precipitates, thereby stabilizing the antimony (Sb) oxyanions in potable water during the chemical treatment process. Therefore, the present study aimed to examine the surface characteristics, size of Fe flocs and coagulation performance of Sb oxyanions under different aqueous matrices. The results showed that surface properties of Fe flocs significantly varies with pH in both Sb(III, V) suspensions, thereby increasing the mobility of Sb(V) ions in alkaline conditions. The negligible change in surface characteristics of Fe flocs was observed in pure water and Sb(III, V) suspension at pH 7. The key role of Van der Waals forces of attraction as well as hydration force in the aggregation of early formed flocs were found, with greater agglomeration capability at higher more ferric chloride dosage. The higher Sb(V) loading decreased the size of Fe flocs and reversed the surface charge of precipitates, resulting in a significant reduction in Sb(V) removal efficiency. The competitive inhibition effect on Sb(III, V) removal was noticed in the presence of phosphate anions, owing to lowering of ζ-potential values towards more negative trajectory. The presence of hydrophobic organic matter (humic acid) significantly altered the surface characteristics of Fe flocs, thereby affecting the coagulation behavior of Sb in water as compared to the hydrophilic (salicylic acid). Overall, the findings of this research may provide a new insight into the variation in physicochemical characteristics of Fe flocs and Sb removal behavior in the presence of inorganic and organic compounds during the drinking water treatment process.     

Catalytic reduction of 4-nitrophenol using synthesized and characterized CoS@MorphcdtH/CoS@4-MPipzcdtH nanoparticles

CoS@MorphcdtH NPs and CoS@4-MPipzcdtH NPs were synthesized by precipitation method involving three mechanisms: inclusion, occlusion, and adsorption. The synthesized NPs were characterized with the help of UV-Vis spectroscopy, FESEM-EDAX, powder x-ray diffraction, TEM, ESIMS, TG/DSC analysis. The morphology of the CoS@MorphcdtH NPs and CoS@4-MPipzcdtH NPs were hexagonal and rectangular, and the particles were in the range 7–12 nm. UV–visible spectral measurements showed surface plasmon resonance at 320 nm–340 nm with band gap of 3.65 eV–3.86 eV. The catalytically active CoSNPs called were investigated for the reduction of 4-nitrophenol (4-NP) via hydrogenation using sodium borohydride (NaBH₄) as a reducing agent. Both the CoS NPs successfully reduced 4-NP to 4- aminophenol (4-AP) in a short time, catalytic performances are almost unchanged for the first five cycles. Herein, we report the preparation and characterizations of efficient active CoS NPs consisting carbodithioic acid framework as a support/capping material, along with catalytic property.     

An analytical approach to solve the fractional-order (2 + 1)-dimensional Wu–Zhang equation

This paper considers time-fractional $(2+1)$-dimensional Wu–Zhang nonlinear system of partial differential equation describing a long dispersive wave. An approximate analytical solution of the dispersion relation of the long wave has been obtained by the fractional reduced differential transform method (FRDTM). The effect of fractional-order $\alpha$ on the wave profile of the solution is discussed graphically and comparing the exact solution of Wu–Zhang equation when $\alpha =1$. The result shows that the present method reveals the effectiveness, efficiency, and reliability of computed mathematical results to easily solve the fractional-order Wu–Zhang (WZ) system of differential equations.