Multiresidue analytical method for the determination of antimicrobials, preservatives, benzotriazole UV stabilizers, flame retardants and plasticizers in fish using ultra high performance liquid chromatography coupled with tandem mass spectrometry

A multiresidue analytical method for the determination of emerging pollutants belonging to personal care products (PCPs) (antimicrobials, preservatives), benzotriazole UV stabilizers (BUVSs) and organophosphorus compounds (OPCs) in fish has been developed using high speed solvent extraction (HSSE) followed by silica gel clean up and ultra fast liquid chromatography coupled with tandem mass spectrometry (UFLC–MS/MS) analysis. Developed extraction and clean up method yielded good recovery (>70%) for all the four groups of emerging pollutants, i.e. antimicrobials (78.5–85.6%), preservatives (85.0–89.4%), BUVSs (70.9–112%) and OPCs (81.6–114%; except for TEP – 68.9% and TPeP – 58.1%) with RSDs ranging from 0.7 to 15.4%. Intra- and inter-day repeatabilities were less than 19.8% and 19.0%, respectively at three spiked levels. The concentrations were given in lipid weight (lw) basis, and the method detection limits were achieved in the lowest range of 0.001–0.006 ng g⁻¹ for two antimicrobials, 0.001–0.015 ng g⁻¹ for four preservatives, 0.0002–0.009 ng g⁻¹ for eight BUVSs and 0.001–0.014 ng g⁻¹ for nine OPCs. Finally, the method was successfully validated as a simple and fast extraction method for the determination of 23 compounds belonging to PCPs, BUVSs and OPCs and applied to the analysis of three species of fish from Manila Bay, the Philippines. Concentrations ranged from 27 to 278 ng g⁻¹ for antimicrobials, 6.61 to 1580 ng g⁻¹ for paraben preservatives, −1 for BUVSs and ND (not detected) to 266 ng g⁻¹ for OPCs suggesting the ubiquitous contamination by these emerging pollutants in Manila Bay. This is the first method developed for the determination of triclocarban, four paraben preservatives and four BUVSs, in fish.     

Structural assignment of monothiocarbonohydrazones by 1H NMR spectroscopy

Analysis of the ¹H NMR spectra of several monothiocarbonohydrazones, some of them synthesized for the first time, shows that they exist as two structural isomers. Whereas, in general, the derivatives of aromatic aldehydes conform to a linear structure, the aliphatic carbonyl derivatives conform to heterocyclic or linear structures, depending on the size of the substituent groups. This dual behaviour is explained in terms of extended conjugation and steric hindrance.     

Electrochemical oxidation of cinnamic acid using stainless steel electrodes

The electro-organic technique is observed to be the modern tool in achieving the oxidation of organic acids to some other useful organic molecules. In the present study, the favourable experimental conditions for carrying out the electrochemical oxidation of cinnamic acid, the experimental set up required and probe for the various products formed have been tried. The anodic process has been carried out at low cost and readily available stainless steel electrode undar aqueous conditions. On identification of the products using chromatographic and spectroscopic techniques, the most probable mechanism has been proposed. To confirm the positive occurrence of the oxidative process under electrolytic conditions, the current — potential study was carried out. The product was analysed by TLC technique, UV and IR spectral studies and identified as 1,4-diphenylbut — 1,3-diene. This work paves a humble way of opening up a new area wherein other electro analytical parameters like polarography, cyclic voltammetry, electrode variation, temperature variation, solvent effects etc. can be studied, along with innumerable substituent effect studies. Paper presented at the 2nd international Conference on Ionic Devices, Anna University, Chennai, India, Nov. 28–30, 2003.     

Recent results from the D? detector

The D? Experiment started taking data in August 1992. We present preliminary results on inclusive jet production, direct photon production, W/Z production and decays, b Physics and first searches fort t production and new particles beyond the Standard Model.     

Two-Stage Flowshop Scheduling Problem with Bicriteria

The two-stage flowshop scheduling problem with the objective of minimizing total flowtime subject to obtaining the optimal makespan is discussed. A branch-and-bound algorithm and two heuristic algorithms have been developed. The results of the experimental investigation of the effectiveness of the algorithms are also presented.     

Enantioseparation of 1-phenyl-1-propanol by supercritical fluid-simulated moving bed chromatography

The enantioseparation of 1-phenyl-1-propanol through the supercritical fluid-simulated moving bed (SF-SMB) process is studied. Non-linear isotherms were measured on an analytical column, and used together with the triangle theory for SMB design to select operating conditions for the SF-SMB. Experiments were carried out on a pilot-scale SF-SMB plant at conditions that corresponded to the non-linear range of the isotherm. Under conditions of low feed concentration, complete separation (extract purity = 99.5%; raffinate purity = 98.4%) was achieved. Under conditions of larger feed concentration, the best separation corresponded to an extract purity of 98.0% and a raffinate purity of 94.0%, and yielded a productivity of 110 g of racemate per kg stationary phase per day.     

Luminescence enhancement induced by aggregation of alkoxy-bridged rhenium(I) molecular rectangles

Self-assembly of rhenium(I)-based molecular rectangles containing long alkyl chains has been achieved in one-pot synthesis by solvothermal methods. An enormous enhancement in the emission intensity, quantum yield, and lifetime of the rectangles has been observed when the solvent medium is changed from organic to aqueous. Addition of water favors the aggregation of Re(I) molecular rectangle resulting in the luminescence enhancement, and this phenomenon has been traced out using light scattering techniques.     

A new synthesis of atanine,khaplofoline and their analogues

A facile synthesis of Atanine, Khaplofoline and their analogues is described. The method involves condensation of an appropriately substituted 2-quinolone-3-acetic acid with isobutryaldehyde, as the starting point.     

Studies on cellulose acetate and sulfonated poly(ether ether ketone) blend ultrafiltration membranes

New ultrafiltration membranes based on chemically and thermally stable arylene main-chain polymers have been prepared by blending the sulfonated poly(ether ether ketone) with cellulose acetate in various compositions in N,N^′-dimethylformamide as solvent by phase inversion technique. Prepared membranes have been subjected to ultrafiltration characterizations such as compaction, pure water flux, water content, and membrane hydraulic resistance. The pore statistics and molecular weight cut-off (MWCO) of the membranes have been estimated using proteins such as trypsin, pepsin, egg albumin and bovine serum albumin. The pore size increased with increasing concentrations of sulfonated poly(ether ether ketone) in the casting solution. Similarly, the MWCOs of the membranes ranged from 20 to 69 kDa, depending on the various polymer compositions. Surface and cross-sectional morphologies of membranes were analyzed using scanning electron microscopy. The effects of polymer compositions on the above parameters were analyzed and the results are compared and discussed with those of pure cellulose acetate membranes.