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Dive into the research topics where A. Chatt is active.

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Featured researches published by A. Chatt.


Analytica Chimica Acta | 1989

Hair analysis : applications in the biomedical and environmental sciences

A. Chatt; Sidney A. Katz; Alan Townshend

This book reviews the theory and practice of using hair as a biopsy tissue for trace elements and discusses the pros and cons of this methodology. The authors examine in detail past and present use of hair trace-element levels as indicators of nutritional status, disease, heavy-metal poisoning and environmental exposure. This book also describes methods for collecting and preparing hair samples for determining their trace-element content. The authors also discuss the various theories explaining the biological incorporation of trace elements into hair and the external factors that may affect trace-element absorption.


Journal of Nanophotonics | 2012

Properties and applications of protein-stabilized fluorescent gold nanoclusters: short review

Daniel M. Chevrier; A. Chatt; Peng Zhang

Research is turning toward nanotechnology for solutions to current limitations in bio- medical imaging and analytical detection applications. New to fluorescent nanomaterials that could help advance such applications are protein-stabilized gold nanoclusters. They are potential candidates for imaging agents and sensitive fluorescence sensors because of their biocompat- ibility and intense photoluminescence. This review discusses the strategy for synthesizing fluorescent protein-gold nanoclusters and the characterization methods employed to study these systems. Optical properties and relevant light-emitting applications are reported to present the versatility of protein-gold nanoclusters. These new bio-nano hybrids are an exciting new system that remains to be explored in many aspects, especially regarding the determination of gold nanocluster local structure and the enhancement of quantum yields. Understanding how to finely tune the optical properties will be pivotal for improving fluorescence imaging and other nanocluster applications. There is a promising future for fluorescent protein-gold nanoclusters as long as research continues to uncover fundamental structure-property relation- ships.


Environmental Pollution | 1997

Extractable organohalogens in tissues of beluga whales from the Canadian Arctic and the St. Lawrence estuary

Joe W. Kiceniuk; J. Holzbecher; A. Chatt

Samples of blubber, brain, kidney, liver, and muscle of individual beluga whales were extracted and analyzed for extractable organic Cl (EOCl), Br (EOBr), and I (EOI) by neutron activation analysis. The highest levels of EOCl (554 microg g(-1) lipid) were found in the kidney of Arctic beluga and the lowest (24 microg g(-1) lipid) in the blubber. Levels in brain and liver lipids were on average of equal magnitude. The unequal distribution of EOCl in tissue lipids is in marked contrast to the equal distribution, in lipid, demonstrated for organochlorines such as DDTs and PCBs by a number of investigations. The distribution of brominated (EOBr) and iodinated (EOI) compounds was similar and markedly different from that of EOCl. The tissue distribution of EOCl seems to be related to the proportion to polar lipids in the tissues. Beluga from St. Lawrence had significantly higher brain EOCl levels than the Arctic samples whereas the levels of EOCl in liver and kidney were higher in the Arctic whales.


Journal of Radioanalytical and Nuclear Chemistry | 1988

Determination of trace elements in food by neutron activation analysis

A. Chatt; H. S. Dang; B. B. Fong; C. K. Jayawickreme; L. S. McDowell; D. L. Pegg

Neutron activation analysis (NAA) methods have been developed for the determination of major, minor and trace elements in duplicate diets and individual food items. These include a cyclic instrumental NAA (CINAA) method for measuring Se content through its short-lived nuclide77mSe; epithermal INAA (EINAA) for I and As; conventional INAA for Br, Ca, Cl, Co, Cr, Fe, K, Mg, Mn, Na, Rb, Sb, Sc, Sn and Zn; combination of EINAA and INAA for Al; radiochemical NAA (RNAA) for As, Au, Co, Cu, Fe, Hg, Mo, Sb, Se and Zn; and preconcentration NAA (PNAA) for U and Th. Accuracy of measurements have been evaluated by analyzing a number of biological and diet reference materials. Multielement concentrations of diets and foods have been measured by these methods.


Geochemistry-exploration Environment Analysis | 2006

The physical and chemical evolution of aerosols in smelter and power plant plumes: an airborne study

Catharine M. Banic; W. Richard Leaitch; Kevin Bruce Strawbridge; Richard Tanabe; H. K. T. Wong; Clément Gariépy; Antonio Simonetti; Zdenek Nejedly; John Campbell; Julia Lu; Jim Skeaff; Dogan Paktunc; J.I. MacPherson; Sreerama M. Daggupaty; Hélène Geonac'h; A. Chatt; Marc Lamoureux

National and international concern about the health effects and continued use of Pb, Cd, As and Hg as well as other metals has defined a need for improved estimates of the long-term risks to ecosystems and human health from metals released from mining, metallurgical and energy production activities. A research aircraft was used to determine the microphysical and chemical properties of airborne particulate metal emissions from the Nanticoke coal-fired power-generating station located on the north shore of Lake Erie, Ontario, and the Horne copper smelter at Rouyn-Noranda, Quebec. These properties are critical to the determination of the deposition rates of the metals emitted, and hence the potential for these species to have impacts on local or distant ecosystems. An overview of the measurements made during the study is given. The size distributions of particles emitted from the stacks and observed within 5 km of the point of emission are briefly described. After dilution by ambient air, the concentration of particles smaller than 0.135 μm in diameter in the plumes is tens of thousands per cubic centimetre, far exceeding the concentrations found in ambient air. However, in the size range 0.135 to 3 μm diameter the plumes generally contribute about one to four times more particles than present in ambient air.


Fresenius Journal of Analytical Chemistry | 1995

Epithermal instrumental neutron activation analysis of biological reference materials for iodine

R. R. Rao; J. Holzbecher; A. Chatt

Epithermal instrumental neutron activation analysis (EINAA) methods have been optimized and applied to several biological reference materials and selected food items for the determination of iodine. The method involves irradiation of the samples for different periods in epi-cadmium and/or epi-boron flux of the Dalhousie University SLOWPOKE-2 reactor and direct counting without any pre-treatment on a 25-cm3 hyperpure Ge detector. The 443 keV photopeak of 128I is used for assaying the iodine content. Precision of measurements, expressed as the relative standard deviation, is 10–15% at 200–500 ppb and 3–12% at 500–6000 ppb levels of iodine. Accuracy of iodine measurements is within 5%. The detection limits for iodine in several biological materials with cadmium and boron, either alone or a combination of the two, as thermal neutron shields have been found to vary between 0.1 and 0.4 mg · kg−1 for different periods of irradiation, decay and counting. The results suggest that the EINAA methods can be successfully applied to biological materials for routine analysis of iodine at levels higher than 200 ppb.


Applied Radiation and Isotopes | 2008

Neutron Activation analysis for Dy, Hf, Rb, Sc and Se in some Ghanaian cereals and vegetables using short-lived nuclides and Compton suppression spectrometry

B. J. B. Nyarko; E.H.K. Akaho; J.J. Fletcher; A. Chatt

A pseudo-cyclic instrumental neutron activation analysis (PCINAA) method has been developed to determine selected elements in various types of cereal and vegetable from Ghana using relatively short-lived nuclides (t1/2<80 s) and the Compton suppression counting. The samples were irradiated for 10 s at the Dalhousie University SLOWPOKE-2 research reactor facility (DUSR) and allowed to decay for 20 s, and counted for 40 s. The process is repeated every 50 s for 4 cycles to quantify Dy, Hf, Rb, Sc and Se through 165mDy, 179Hf, 86mRb, 46mSc, and 77mSe. The detection limits were generally of the order of 1.0 ng g(-1) except for Rb which is about 1 microg g(-1). Both precision and accuracy of the method were found to be good.


Journal of Radioanalytical and Nuclear Chemistry | 1987

Determination of selenium in individual food items using the short-lived nuclide77mSe

L. S. McDowell; P. R. Giffen; A. Chatt

The selenium content of a variety of food items representing a normal hospital diet has been determined by cyclic instrumental neutron activation analysis (CINAA) through the 162-keV gamma-ray of the77mSe nuclide. The CINAA method is very simple and rapid. It involves irradiation of a sample for 20 s, decay for 20 s, and counting for 20 s. The precision of the method has been significantly improved by recycling the samples up to 4 times. The accuracy has been evaluated by analyzing a number of certified reference materials of varied selenium levels.


Analytica Chimica Acta | 1987

Analysis for trace elements with a slowpoke reactor

D.E. Ryan; A. Chatt; J. Holzbecher

Abstract The SLOWPOKE reactor is very useful for neutron activation analysis and has been in operation at Dalhousie University for ten years. Improvements to the reactor are out-lined and flux evaluations after major changes are reported. Its use for the determination of trace elements in a broad variety of materials is described.


Analytica Chimica Acta | 1983

Determination of gold in silicate rocks and ores by coprecipitation with tellurium and neutron activation—γ-spectrometry

C.M. Elson; A. Chatt

Abstract The method described for determining ultra-trace levels of gold in geological materials and water samples involves the coprecipitation of gold with elemental tellurium followed by neutron activation of the precipitate. Gold-198 is measured, with detection and determination limits of 0.7 and 2.3 ng Au g−1, respectively. The main interferences in the γ-spectrum are due to tellurium, iodine, and bromine, all of which were significantly reduced by evaporation without the loss of gold. The method also collects palladium and rhodium quantitatively.

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Rongchao Jin

Carnegie Mellon University

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