Elements Of X Ray Diffraction

Since their introduction in the late 1970s, sequential extraction procedures have experienced a rapid increase in use. They are now applied for a large number of potentially toxic elements in a wide range of sample types. This review uses evidence from the literature to consider the usefulness and limitations of sequential extraction and thereby to assess its future role in environmental chemical analysis. It is not the intention to provide a comprehensive survey of all applications of sequential extractions or to consider the merits and disadvantages of individual schemes. These aspects have been covered adequately in other, recent reviews. This review focuses in particular on various key issues surrounding sequential extractions such as nomenclature, methodologies, presentation of data and interpretation of data, and discusses typical applications from the recent literature for which sequential extraction can provide useful and meaningful information. Also covered are emerging developments such as accelerated procedures using ultrasound- or microwave energy-assisted extractions, dynamic extractions, the use of chemometrics, the combination of sequential extraction with isotope analysis, and the extension of the approach to non-traditional analytes such as arsenic, mercury, selenium and radionuclides.

Is there a future for sequential chemical extraction

The micronucleus (MN) assay in exfoliated buccal cells is a useful and minimally invasive method for monitoring genetic damage in humans. This overview has concluded that although MN assay in buccal cells has been used since the 1980s to demonstrate cytogenetic effects of environmental and occupational exposures, lifestyle factors, dietary deficiencies, and different diseases, important knowledge gaps remain about the characteristics of micronuclei and other nuclear abnormalities, the basic biology explaining the appearance of various cell types in buccal mucosa samples and effects of diverse staining procedures and scoring criteria in laboratories around the world. To address these uncertainties, the human micronucleus project (HUMN; see http://www.humn.org) has initiated a new international validation project for the buccal cell MN assay similar to that previously performed using human lymphocytes. Future research should explore sources of variability in the assay (e.g. between laboratories and scorers, as well as inter- and intra-individual differences in subjects), and resolve key technical issues, such as the method of buccal cell staining, optimal criteria for classification of normal and degenerated cells and for scoring micronuclei and other abnormalities. The harmonization and standardization of the buccal MN assay will allow more reliable comparison of the data among human populations and laboratories, evaluation of the assay's performance, and consolidation of its world-wide use for biomonitoring of DNA damage.

The micronucleus assay in human buccal cells as a tool for biomonitoring DNA damage: The HUMN project perspective on current status and knowledge gaps

The simultaneous entrapment of biological macromolecules and nanostructured silica-coated magnetite in sol-gel materials using a reverse-micelle technique leads to a bioactive, mechanically stable, nanometer-sized, and magnetically separable particles. These spherical particles have a typical diameter of 53 +/- 4 nm, a large surface area of 330 m(2)/g, an average pore diameter of 1.5 nm, a total pore volume of 1.427 cm(3)/g and a saturated magnetization (M(S)) of 3.2 emu/g. Peroxidase entrapped in these particles shows Michaelis-Mentan kinetics and high activity. The catalytic reaction will take place immediately after adding these particles to the reaction solution. These enzyme entrapping particles catalysts can be easily separated from the reaction mixture by simply using an external magnetic field. Experiments have proved that these catalysts have a long-term stability toward temperature and pH change, as compared to free enzyme molecules. To further prove the application of this novel magnetic biomaterial in analytical chemistry, a magnetic-separation immunoassay system was also developed for the quantitative determination of gentamicin. The calibration for gentamicin has a working range of 200-4000 ng/mL, with a detection limit of 160 ng/mL, which is close to that of the fluorescent polarization immunoassay (FPIA) using the same reactants.

Magnetite-containing spherical silica nanoparticles for biocatalysis and bioseparations （vol 76, pg 1316, 2004）

https://orbit.dtu.dk/files/152734893/Krzeminski2018_PostPrint_Performance_of_secondary_wastewater_treatment_methods_for_the_removal_of_contaminants.pdf

Performance of secondary wastewater treatment methods for the removal of contaminants of emerging concern implicated in crop uptake and antibiotic resistance spread: A review

Ion chromatography–inductively coupled plasma-mass spectrometry (IC–ICP-MS) was used for the identification and quantification of chromium species. Chromium(III) and chromium(VI) were separated and...

Simultaneous Determination of Chromium Species in Water and Plant Samples at Trace Levels by Ion Chromatography–Inductively Coupled Plasma-Mass Spectrometry

In situ atom trapping of Bi on W-coated slotted quartz tube flame atomic absorption spectrometry and interference studies

Speciation Studies in Soil, Sediment and Environmental Samples

A novel, ecofriendly, and easy extraction and preconcentration method named as vortex-assisted spraying-based fine droplet formation liquid-phase microextraction was proposed for the determination of prochloraz at trace levels in orange juice samples by gas chromatography-mass spectrometry (GC-MS). In this novel system, extraction solvent is dispersed by the help of spraying apparatus instead of dispersive solvent. Various parameters of the method were carefully optimized to increase signal-to-noise ratio of the analyte. Under the optimum chromatographic and extraction conditions, limit of detection and limit of quantification were calculated as 3.2 and 10.8 μg/kg, respectively. Moreover, enhancement in quantification power for the GC-MS system was determined as 372 folds based on LOQ comparison. Relative recovery results for orange juice samples were found to be between 95.0-107.7% by utilizing matrix matching calibration. Furthermore, the developed method may be used to efficiently and simply extract other organic compounds for their determinations in several matrices.

A novel and rapid extraction protocol for sensitive and accurate determination of prochloraz in orange juice samples: Vortex-assisted spraying-based fine droplet formation liquid-phase microextraction before gas chromatography-mass spectrometry.

Digestion methods such as dry and wet ashing and microwave oven were examined at various conditions to determine a rapid, reliable, and simple digestion procedure for yogurt. Digestion by microwave oven was found to be an excellent method in comparison with dry and wet ashing methods when only Al and Zn in yogurt samples were determined. Iron in this matrix is not completely digested by the microwave oven method at the examined conditions. From the obtained results, yogurt can also be a good source of essential nutrients such as minerals in human diet, especially zinc. Aluminum concentrations in yogurt samples fermented in Al containers were found to be significantly higher than in plastic containers. Al concentrations of yogurt taken from the bottom of the container were found to be higher than from the center and top of Al containers. The determinations of metals were carried out via an atomic absorption spectrophotometer using calibration curve and standard additions methods. Aluminum concentr...

Sezgin Bakırdere

Papers

Simultaneous Determination of Chromium Species in Water and Plant Samples at Trace Levels by Ion Chromatography–Inductively Coupled Plasma-Mass Spectrometry

In situ atom trapping of Bi on W-coated slotted quartz tube flame atomic absorption spectrometry and interference studies

Speciation Studies in Soil, Sediment and Environmental Samples

A novel and rapid extraction protocol for sensitive and accurate determination of prochloraz in orange juice samples: Vortex-assisted spraying-based fine droplet formation liquid-phase microextraction before gas chromatography-mass spectrometry.

Comparison of Dry, Wet, and Microwave Ashing Methods for the Determination of Al, Zn, and Fe in Yogurt Samples by Atomic Absorption Spectrometry