Individual and simultaneous electrochemical determination of metanil yellow and curcumin on carbon quantum dots based glassy carbon electrode.

Adulteration of medicinally valuable curcumin (CU) with harmful chemicals as metanil yellow (MY) in recent years have demanded for quick detection techniques of the adulterants. The voltammetric behavior of CU and MY on bare glassy carbon electrode (BGCE) and carbon quantum dots modified glassy carbon electrode (CQDs/GCE) was studied by both cyclic voltammetry (CV) and differential pulse voltammetry (DPV) in phosphate buffer solution of pH 5.4.

Electrochemical synthesis of a gold atomic cluster-chitosan nanocomposite film modified gold electrode for ultra-trace determination of mercury.

Gold atomic cluster based nanocomposites are important in the field of energy and sensing applications due to their interesting optical, electronic, chemical and catalytic properties. In the present study a chitosan stabilized gold atomic cluster nanocomposite was synthesised by a simple electrochemical technique based on the anodic dissolution of a gold electrode in the presence of a cationic surfactant, cetyl trimethyl ammonium bromide (CTAB), and a biopolymer, chitosan, on a gold electrode. The gold clusters formed were characterized by DLS, TEM, MALDI-TOF-MS, XPS, fluorescence and cyclic voltammetry.

Bio-based ionic liquid crystalline quaternary ammonium salts: properties and applications.

In the present work, we describe the preparation, properties, and applications of novel ionic liquid crystalline quaternary ammonium salts (QSs) of 3-pentadecylphenol, a bio-based low-cost material derived from cashew nut shell liquid. Amphotropic liquid crystalline phase formation in QSs was characterized using a combination of techniques, such as DSC, PLM, XRD, SEM, and rheology, which revealed the formation of one, two, and three dimensionally ordered mesophases in different length scales. On the basis of these results, a plausible mechanism for the formation of specific modes of packing in various mesophases was proposed.

Ultrasensitive voltammetric determination of catechol at a gold atomic cluster/poly(3,4-ethylenedioxythiophene) nanocomposite electrode.

A novel gold atomic cluster-poly(3,4-ethylenedioxythiophene) (AuAC/PEDOT/Au) nanocomposite modified gold electrode has been designed for the trace level sensing of catechol. The addition of copper(II) enhanced the electro-catalytic oxidation of catechol via the formation of copper(I). The electrochemically synthesized PEDOT/Au and the AuAC/PEDOT/Au hybrid films were characterized by electrochemical and morphological methods.

Mixed monolayer protected gold atom-oxide cluster synthesis and characterization.

Small atomic gold clusters in solution, Au(n), stabilized by cetyl trimethylammonium bromide (CTAB) and cysteine, have been synthesized potentiodynamically in quiescent aqueous solutions. The electrodissolution of gold to gold ions during an anodic scan and subsequent cluster formation during a cathodic scan in underpotential (UPDD) and overpotential dissolution-deposition (OPDD) regions were studied. The experimental potentiodynamic I-E profiles and chronoamperometric i-t transients are fit into reported theoretical models of adsorption and electrocrystallization.

In situ copper oxide modified molecularly imprinted polypyrrole film based voltammetric sensor for selective recognition of tyrosine.

Organic-inorganic hybrids are promising functional materials as they combine the special characteristics of both organic (polymer) and inorganic phases. Among different existing approaches for the preparation of such polymer-inorganic hybrid coatings, in situ electrochemical methods are very advantageous because of their high sensitivity and simplicity. In the present study, voltammetric sensors for tyrosine are designed and developed via various modifications on glassy carbon electrode such as polypyrrole coated GCE, molecularly imprinted polypyrrole coated GCE (MIPPy) and in situ copper oxide modified MIPPy coated GCE.

Hybrid gold atomic cluster-cobalt oxide scaffolds for dual tandem electrocatalytic sensing of cysteine.

Innovations in nanoelectrochemistry have opened a plethora of techniques for the preparation of nanometer sized electrochemical probes with tunable properties. Atomic clusters emerged at the crossroad of physics and chemistry has immense potential as novel "electron antennaes" in electrocatalysis. Herein, we report the electrochemical synthesis and the synergistic electrocatalytic effect of metal oxide supported gold atomic clusters for subnanomolar level sensing of cysteine.

Ion imprinted polymer particles for separation of yttrium from selected lanthanides.

Lanthanide(III) (Dy, Gd, Tb and Y) ion imprinted polymer (IIP) materials were synthesized via single pot reaction by mixing lanthanide imprint ion with 5,7-dichloroquinoline-8-ol, 4-vinylpyridine, styrene, divinylbenzene and 2,2'-azobisisobutyronitrile in 2-methoxyethanol porogen. The imprint ion was removed by stirring the above materials (after powdering) with 6 mol/L HCl to obtain the respective lanthanide IIP particles. Y-Dy, Y-Gd and Dy-Gd polymer particles were obtained by physically mixing equal amounts of the respective leached individual lanthanide(III) particles.

Removal of toxic uranium from synthetic nuclear power reactor effluents using uranyl ion imprinted polymer particles.

Major quantities of uranium find use as nuclear fuel in nuclear power reactors. In view of the extreme toxicity of uranium and consequent stringent limits fixed by WHO and various national governments, it is essential to remove uranium from nuclear power reactor effluents before discharge into environment. Ion imprinted polymer (IIP) materials have traditionally been used for the recovery of uranium from dilute aqueous solutions prior to detection or from seawater.

Selective recognition of neodymium (III) using ion imprinted polymer particles.

Neodymium (III) ion-imprinted polymer (IIP) materials were prepared by the copolymerization of neodymium (III)-5,7-dichloroquinoline-8-ol-4-vinylpyridine ternary complex with styrene(monomer), divinyl benzene (crosslinking monomer) in the presence of 2,2'-azobisisobutyronitrile (initiator). The synthesis was carried out in 2-methoxy ethanol medium (porogen) and the resultant material was filtered, washed, dried and powdered to form unleached IIP particles. The imprint ion was removed by stirring the above particles with 50% (v/v) HCl for 6 h to obtain leached IIP particles with cavities in the polymer particles.