Indirect complexometric titration of potassium,rubidium, cesium,thallium and ammonium

A titrimetric method using EDTA for the determination of potassium, rubidium, cesium, thallium and ammonium has been developed. These cations are precipitated as M₂Ag[Co(NO₂)₆] and the blue cobalt thiocyanate complex in acetone-water mixed system is titrated with EDTA. Milligram quantities have been determined in the present work     

Gas-liquid partition chromatography : Column behavior and its reproduction criteria for favorable column behavior

The distribution of a solute in a gas-liquid Chromatographic column has been discussed from the probability view point and its analogy to the Bernoulli trial system has been shown. It has been shown that the reproduction of column behavior is possible by reproducing the probability. The criterion for the optimum column temperature has also been discussed. Recommendations have been made for determining the optimum column conditions and its reproduction.     

Indirect complexometric titration of sodium and potassium with EDTA

Summary Sodium is precipitated as sodium zinc uranyl acetate, filtered and dissolved in water, and zinc is titrated with EDTA using eriochrome black T as indicator. Potassium is precipitated as potassium sodium cobaltinitrite and dissolved in hot water containing little hydrochloric acid. The blue colored solution produced by cobalt in solution, with ammonium thiocyanate and acetone was titrated with EDTA until colorless. The results are good.The author is grateful to Prof. Philip W. West, Boyd Professor of Chemistry, Louisiana State University, for kindly providing the facilities to carry out the investigation.     

HSAB principle applied to the time evolution of chemical reactions

Time evolution of various reactivity parameters such as electronegativity, hardness, and polarizability associated with a collision process between a proton and an X- atom/ion (X = He, Li(+), Be(2+), B(3+), C(4+)) in its ground ((1)S) and excited((1)P,(1)D,(1)F) electronic states as well as various complexions of a two-state ensemble is studied using time-dependent and excited-state density functional theory. This collision process may be considered to be a model mimicking the actual chemical reaction between an X-atom/ion and a proton to give rise to an XH(+) molecule. A favorable dynamical process is characterized by maximum hardness and minimum polarizability values according to the dynamical variants of the principles of maximum hardness and minimum polarizability. An electronic excitation or an increase in the excited-state contribution in a two-state ensemble makes the system softer and more polarizable, and the proton, being a hard acid, gradually prefers less to interact with X as has been discerned through the drop in maximum hardness value and the increase in the minimum polarizability value when the actual chemical process occurs. Among the noble gas elements, Xe is the most reactive. During the reaction: H(2) + H(+) --> H(3)(+) hardness maximizes and polarizability minimizes and H(2) is more reactive in its excited state. Regioselectivity of proton attack in the O-site of CO is clearly delineated wherein HOC(+) may eventually rearrange itself to go to the thermodynamically more stable HCO(+).     

Spectrophotometric determination of gold with phenyl-α-pyridyl ketoxime

A method is described for the spectrophotometric determination of gold in the concentration range of 2 to 16 p.p.m. using phenyl-α-pyridyl ketoxime as the reagent. The reagent permits to detect Iμ of gold in I ml of a solution. The method is particularly free from interference by the ions with which gold is frequently associated.     

Design and Development of Ultrafast Sinapic Acid Sensor Based on Electrochemically Nanotuned Gold Nanoparticles and Solvothermally Reduced Graphene Oxide

We report for the first time sinapic acid (SA) sensing based on nanocomposite comprising electrochemically tuned gold nanoparticles (EAuNPs) and solvothermally reduced graphene oxide (rGO). The synthesized EAuNPs, rGO, and EAuNPs‐rGO nanocomposite were characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), particle size analysis, and Raman spectroscopy. A proof‐of‐concept electrochemical sensor for SA was developed based on synthesized EAuNPs‐rGO nanocomposite, which was characterized by electrochemical techniques such as cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The developed sensor detected SA with a linear dynamic range (LDR) between 20 μM and 200 μM and detection limit (DL) of 33.43 (±0.21) nM (RSD<3.32 %). To show the useful purpose of the sensor probe in clinical applications, SA was detected in human urine samples, which showed the percentage recovery between 82.6 % and 92.8 %. Interferences due to various molecules such as L‐cystine, glycine, alanine, serum albumin, uric acid, citric acid, ascorbic acid, and urea were tested. Long‐term stability of the sensor probe was examined, which was found to be stable up to 6 weeks. The sensor fabricated using EAuNPs‐rGO nanocomposite has many attractive features such as; simplicity, rapidity, and label‐free detection; hence, it could be a method of choice for SA detection in various matrices.     

Highly sensitive method for the determination of omeprazole in human plasma by liquid chromatography-electrospray ionization tandem mass spectrometry: application to a clinical pharmacokinetic study

A highly sensitive, rapid assay method has been developed and validated for the estimation of omeprazole (OPZ) in human plasma with liquid chromatography coupled to tandem mass spectrometry with electrospray ionization in the positive-ion mode. The assay procedure involves alkalinization of plasma followed by simple liquid-liquid extraction of OPZ and lansoprazole (internal standard, IS) from human plasma with acetonitrile. Chromatographic separation was achieved with 0.01 M ammonium acetate:acetonitrile (40:60, v/v) at a flow rate of 0.25 mL/min on an Inertsil ODS 3 column with a total run time 2.5 min. The MS/MS ion transitions monitored were 346.1 --> 198.1 for OPZ and 370.1 --> 252.1 for IS. Method validation and clinical sample analysis were performed as per FDA guidelines and the results met the acceptance criteria. The lower limit of quantitation achieved was 0.05 ng/mL and the linearity was observed from 0.05 to 10.0 ng/mL. The intra-day and inter-day precisions were in the ranges 2.09-8.56 and 5.29-8.19%, respectively. This novel method has been applied to a pharmacokinetic study of OPZ in humans.     

αPicolinic acid as a colorimetric reagent : Determination of iron and aluminium

A new spot test for stannous tin has been evolved, using the ammonium salt of 6-nitro-2-naphthylamine-8-sulphonic acid as reagent, an intense blue fluorescence being produced under ultraviolet light. Of 47 metallic ions tested only Sn⁺² fluoresced under the conditions of the test, as little as one microgram being capable of detection.     

Alternative Strategies for the Calibration and Elimination of Matrix Effects in LC-MS/MS Multiresidue Analysis of Tea Matrix

Journal of Analytical Chemistry - Efficiency of four different calibration techniques was evaluated on 50 pesticides in tea matrix by LC-MS/MS. Further statistical testing by MANOVA, T-tests as...     

Engineered Nanomaterial Assisted Signal‐amplification Strategies for Enhancing Analytical Performance of Electrochemical Biosensors

The design and development of modern biosensors for sensitive and selective detection of various biomarkers is important in diversified arenas including healthcare, environment, and food industries etc. The requirement of more robust and reliant biosensors lead to the development of various sensing modules. The nanomaterials having specific optical, electrical, and mechanical strength can pave the way towards development of ultrafast, robust, and miniaturized modules for biosensors. It can provide not only the point‐of‐care applicability but also has tremendous commercial as well as industrial justification. In order to improve the performance of the sensor systems, various nanostructure materials have been readily studied and applied for development of novel biosensors. In the last few years, researchers are engaged on harnessing the unique atomic and molecular properties of advance‐engineered materials including carbon nanotubes, graphene nanosheets, metal nanoparticles, metal oxide nanoparticles, and their nano‐conjugates. In view of such recent developments in nanomaterial engineering, the current review has been formulated emphasizing the role of these materials in surface engineering, biomolecule conjugation, and signal amplification for development of various ultrasensitive and robust biosensors having commercial as well as industrial viability. Attention is given on the electrochemical biosensors incorporating various nanomaterials and their conjugates. Importance of nanomaterials in the analytical performance of the various biosensor has also been discussed. To put a perceptive insights on the importance of various nanomaterials, an extended table is incorporated, which includes probe design, analyte, LOD, and dynamic range of various electrochemical biosensors.