An investigation of changes in element distribution and chemical states during differentiation of embryonic stem cells

International Nuclear Information System (INIS)

Sugimoto, T.; Ide-Ektessabi, A.; Ishihara, R.; Tanigaki, M.

2004-01-01

Metallic elements and their organic compounds have dynamic regulatory functions in cells. In this study, we implemented a new approach to investigate the mechanism of differentiation of embryonic stem cells, by measuring and analyzing the change in distribution and chemical states of intracellular trace elements. We anticipate that trace metal elements and metalloproteins play important roles in the direction of differentiation, both as active centers, and as factors in the death of neural cells in neurodegenerative disorders. The aim of this study is to analyze the distribution and chemical states of trace elements during the process of differentiation of mouse embryonic stem cells, and to understand how these factors relate to the differentiation process. Using the experimental results, some previously unexplained points are considered, namely (1) how the intracellular elements change during the process of neuronal differentiation, and (2) what the optimal conditions of such elements are for neuronal differentiation. The information obtained during this study is relevant to nervous system development and evolution

An investigation of changes in element distribution and chemical states during differentiation of embryonic stem cells

Energy Technology Data Exchange (ETDEWEB)

Sugimoto, T.; Ide-Ektessabi, A. E-mail: h51167@sakura.kudpc.kyoto-u.ac.jp; Ishihara, R.; Tanigaki, M

2004-07-01

Metallic elements and their organic compounds have dynamic regulatory functions in cells. In this study, we implemented a new approach to investigate the mechanism of differentiation of embryonic stem cells, by measuring and analyzing the change in distribution and chemical states of intracellular trace elements. We anticipate that trace metal elements and metalloproteins play important roles in the direction of differentiation, both as active centers, and as factors in the death of neural cells in neurodegenerative disorders. The aim of this study is to analyze the distribution and chemical states of trace elements during the process of differentiation of mouse embryonic stem cells, and to understand how these factors relate to the differentiation process. Using the experimental results, some previously unexplained points are considered, namely (1) how the intracellular elements change during the process of neuronal differentiation, and (2) what the optimal conditions of such elements are for neuronal differentiation. The information obtained during this study is relevant to nervous system development and evolution.

A scalable machine-learning approach to recognize chemical names within large text databases

Directory of Open Access Journals (Sweden)

Wren Jonathan D

2006-09-01

Full Text Available Abstract Motivation The use or study of chemical compounds permeates almost every scientific field and in each of them, the amount of textual information is growing rapidly. There is a need to accurately identify chemical names within text for a number of informatics efforts such as database curation, report summarization, tagging of named entities and keywords, or the development/curation of reference databases. Results A first-order Markov Model (MM was evaluated for its ability to distinguish chemical names from words, yielding ~93% recall in recognizing chemical terms and ~99% precision in rejecting non-chemical terms on smaller test sets. However, because total false-positive events increase with the number of words analyzed, the scalability of name recognition was measured by processing 13.1 million MEDLINE records. The method yielded precision ranges from 54.7% to 100%, depending upon the cutoff score used, averaging 82.7% for approximately 1.05 million putative chemical terms extracted. Extracted chemical terms were analyzed to estimate the number of spelling variants per term, which correlated with the total number of times the chemical name appeared in MEDLINE. This variability in term construction was found to affect both information retrieval and term mapping when using PubMed and Ovid.

Chemical and nuclear properties of Rutherfordium (Element 104)

International Nuclear Information System (INIS)

Kacher, C.D.

1995-01-01

The chemical-properties of rutherfordium (Rf) and its group 4 homologs were studied by sorption on glass support surfaces coated with cobalt(II)ferrocyanide and by solvent extraction with tributylphosphate (TBP) and triisooctylamine (TIOA). The surface studies showed that the hydrolysis trend in the group 4 elements and the pseudogroup 4 element, lb, decreases in the order Rf>Zr∼Hf>Th. This trend was attributed to relativistic effects which predicted that Rf would be more prone to having a coordination number of 6 than 8 in most aqueous solutions due to a destabilization of the 6d 5/2 shell and a stabilization of the 7p l/2 shell. This hydrolysis trend was confirmed in the TBP/HBr solvent extraction studies which showed that the extraction trend decreased in the order Zr>Hf>Rf?Ti for HBr, showing that Rf and Ti did not extract as well because they hydrolyzed more easily than Zr and Hf. The TIOA/HF solvent extraction studies showed that the extraction trend for the group 4 elements decreased in the order Ti>Zr∼Hf>Rf, in inverse order from the trend of ionic radii Rf>Zr∼Hf>Ti. An attempt was made to produce 263 Rf (a) via the 248 Cm( 22 Ne, α3n) reaction employing thenoyltrifluoroacetone (TTA) solvent extraction chemistry and (b) via the 249 Bk( 18 O,4n) reaction employing the Automated Rapid Chemistry Apparatus (ARCA). In the TTA studies, 16 fissions were observed but were all attributed to 256 Fm. No alpha events were observed in the Rf chemical fraction. A 0.2 nb upper limit production cross section for the 248 Cm( 22 Ne, α3n) 263 Rf reaction was calculated assuming the 500-sec half-life reported previously by Czerwinski et al. [CZE92A

An Educational Card Game for Learning Families of Chemical Elements

Science.gov (United States)

Mariscal, Antonio Joaquin Franco; Martinez, Jose Maria Oliva; Marquez, Serafin Bernal

2012-01-01

This paper describes an educational card game designed to help high school students (grade 10, 15-16 years old) "understand," as opposed to memorize, the periodic table. The game may also be used to identify different chemical elements found in daily life objects. As an additional value, students learn the names and symbols of the displayed…

Soil-leaf transfer of chemical elements for the Atlantic Forest

International Nuclear Information System (INIS)

Joacir De Franca, E.; De Nadai Fernandes, E.A.; Bacchi, M.A.; Tagliaferro, F.S.

2007-01-01

Soil analysis could improve environmental studies since soil is the main source of chemical elements for plants. In this study, soil samples collected at 0-10 cm depth under tree crown projection were analyzed by INAA. Using the chemical composition of the leaf previously determined, the leaf-soil transfer factors of chemical elements could be estimated for the Atlantic Forest. Despite the variability of the intra-species, the transfer factors were specific for some plant species due to their element accumulation in the leaves. Similar Br-Zn combined transfer factors were obtained for the species grouped according to habitats in relation to their position (understory or dominant species) in the forest canopy. (author)

Transuranium elements: Past, present, and future

International Nuclear Information System (INIS)

Seaborg, G.T.

1995-01-01

In this illustrative Account the authors shall concentrate on four of these elements, chosen for their current interest or pivotal role. The story of plutonium is one of the most dramatic in the history of science, and today, plutonium is at the focus of an extraordinary dilemma. Mendelevium (element 101) has played a pivotal role in blazing the trail for the discovery of the heaviest elements on the basis of open-quotes one atom at a timeclose quotes production. Seaborgium (element 106) was recently named in my honor by the discoverers and may be the last element, at least for some time, for which it will be possible to determine many chemical properties. And element 110 represents recent evidence, after a lapse of 10 years, for the discovery of a chemical element. Recent (1994) recommendations of the IUPAC Commission on the Nomenclature of Inorganic Chemistry for the renaming of elements 104-108 have met with widespread rejection. The author is using the names proposed by the acknowledged discoverers (elements 106-109) or, in the case of the disputed elements 104 and 105, the most logical names. 21 refs., 5 figs

Use of chemical elements of 1A family by tropical tree species

International Nuclear Information System (INIS)

Carmo, Andrius M.J.; Paiva, Jose Daniel S. de; Magalhaes, Marcelo R.L. de; Franca, Elvis J. de; Hazin, Clovis A.; Bacchi, Marcio A.; Fernandes, Elisabete A.N.

2013-01-01

This study aims to evaluate the distribution of K, Rb and Cs in leaves of trees of the Atlantic Forest through studies of correlation between the chemical elements. For this, we used the Instrumental Neutron Activation Analysis for the quantification of the chemical elements. The concentration ranges found were 6700-24000 mg / kg for K, 16 to 72mg / kg for Rb and 0.08 to 0,92mg / kg for Cs. As Rb has chemical similarity to K, is easily absorbed by plants, leading to a high value (0.9) of the Pearson correlation. For the correlation between K and Cs, no significant values were detected except for some species of the Myrtaceae family. However, average correlations (0.6 < r <0.8) between Rb-Cs were obtained for seven plant species of different families. The absence of a specific pattern using of K, Rb and Cs by plants showed great complexity in the distribution of chemical elements in the ecosystem

Atlantic Forest. A natural reservoir of chemical elements

International Nuclear Information System (INIS)

De Franca, E.J.; De Nadai Fernandes, E.A.; Bacchi, M.A.; Elias, C.

2008-01-01

The accumulation of chemical elements in biological compartments is one of the strategies of tropical species to adapt to a low-nutrient soil. This study focuses on the Atlantic Forest because of its eco-environmental importance as a natural reservoir of chemical elements. About 20 elements were determined by INAA in leaf, soil, litter and epiphyte compartments. There was no seasonality for chemical element concentrations in leaves, which probably indicated the maintenance of chemical elements in this compartment. Considering the estimated quantities, past deforestation events could have released large amounts of chemical elements to the environment. (author)

Recent studies of nuclear and chemical properties of elements 103, 104 and 105

International Nuclear Information System (INIS)

Hoffman, D.C.

1990-08-01

Information obtained since 1983 on the nuclear and chemical properties of element 103, the last on the actinide series, and elements 104 and 105, at the beginning of the transactinide series, is reviewed. Their chemical properties are compared with their lanthanide and lighter group 4 and 5 homologs and evidence for possible relativistic effects is discussed. The current knowledge of the nuclear properties of these elements and how these affect of the study of chemical properties is discussed. Some of the challenges involved in the study of short-lived isotopes which can only be produced an ''atom-at-a-time'' at an appropriate accelerator and the prognosis for future studies of these and still heavier elements are considered. 40 refs., 4 figs

What's in a name? Group fitness class names and women's reasons for exercising.

Science.gov (United States)

Brown, Theresa C; Miller, Bridget M; Adams, Bailey M

2017-01-01

The benefits of intrinsic exercise motivation are well recognized, yet extrinsically focused group-fitness class names/descriptions dominate the fitness industry. To explore the impact of how fitness classes are marketed, women (N = 389) were asked to indicate their preference for either intrinsically or extrinsically focused fitness classes based on title/description. Participants who favored intrinsic class names/descriptions were more likely to report greater interest/enjoyment, perceived competence, and greater effort and report exercising for health/fitness-related reasons. Those favoring extrinsic class names/descriptions were more likely to experience tension/pressure when exercising and report exercising for appearance/weight-related reasons. The results demonstrate the importance of wording when marketing fitness classes.

Chemical and nuclear properties of Rutherfordium (Element 104)

Energy Technology Data Exchange (ETDEWEB)

Kacher, Christian D. [Univ. of California, Berkeley, CA (United States)

1995-10-30

The chemical-properties of rutherfordium (Rf) and its group 4 homologs were studied by sorption on glass support surfaces coated with cobalt(II)ferrocyanide and by solvent extraction with tributylphosphate (TBP) and triisooctylamine (TIOA). The surface studies showed that the hydrolysis trend in the group 4 elements and the pseudogroup 4 element, lb, decreases in the order Rf>Zr≈Hf>Th. This trend was attributed to relativistic effects which predicted that Rf would be more prone to having a coordination number of 6 than 8 in most aqueous solutions due to a destabilization of the 6d_5/2 shell and a stabilization of the 7p_I/2 shell. This hydrolysis trend was confirmed in the TBP/HBr solvent extraction studies which showed that the extraction trend decreased in the order Zr>Hf>Rf?Ti for HBr, showing that Rf and Ti did not extract as well because they hydrolyzed more easily than Zr and Hf. The TIOA/HF solvent extraction studies showed that the extraction trend for the group 4 elements decreased in the order Ti>Zr≈Hf>Rf, in inverse order from the trend of ionic radii Rf>Zr≈Hf>Ti. An attempt was made to produce ²⁶³Rf (a) via the ²⁴⁸Cm(²²Ne, α3n) reaction employing thenoyltrifluoroacetone (TTA) solvent extraction chemistry and (b) via the ²⁴⁹Bk(¹⁸O,4n) reaction employing the Automated Rapid Chemistry Apparatus (ARCA). In the TTA studies, 16 fissions were observed but were all attributed to ²⁵⁶Fm. No alpha events were observed in the Rf chemical fraction. A 0.2 nb upper limit production cross section for the ²⁴⁸Cm(²²Ne, α3n)²⁶³Rf reaction was calculated assuming the 500-sec half-life reported previously by Czerwinski et al. [CZE92A].

Mass spectrographic analysis of selected chemical elements by microbial leaching of zircon

International Nuclear Information System (INIS)

Becker, S.; Dietze, H.J.; Bullmann, M.; Iske, U.

1986-01-01

Spark source mass spectrometry is a useful method for chemical element analysis of geological and biological samples. This sensitive technique (detection limit down to the ppb-range) is used to analyze leaching processes by means of several microorganisms. The problem of microbial leaching of chemical resistent materials was tested under laboratory conditions with regard to possible analytical and technical applications. Leaching of metals with chemolithotrophic and heterotrophic, organic acids producing microorganisms has been investigated with zircon from the Baltic Shield containing 0.7% rare earth elements and 1.67% hafnium. When zircon is leached with strains of thiobacillus ferrooxidans about 80% of the rare earth elements, Hf, Th and U can be recovered. (orig.) [de

Group separation of rare earth elements by liquid-liquid extraction for the neutron activation analysis of silicate rocks

International Nuclear Information System (INIS)

Wyttenbach, A.; Bajo, S.; Tobler, L.

1983-01-01

Rare earth elements are isolated as a group from neutron activated rock samples by a new radiochemical procedure based on extraction with thenoyltrifluoracetone/phenanthroline in CHCl 3 . The procedure consists of three extraction steps, obviates the use of inactive carriers and gives practically quantitative chemical yields, thereby avoiding fractionation of the individual rare earths. Details of the dissolution, chemical separations. and counting procedure are given together with an analysis of BCR-1. (author)

An Alternate Graphical Representation of Periodic table of Chemical Elements

OpenAIRE

Abubakr, Mohd

2009-01-01

Periodic table of chemical elements symbolizes an elegant graphical representation of symmetry at atomic level and provides an overview on arrangement of electrons. It started merely as tabular representation of chemical elements, later got strengthened with quantum mechanical description of atomic structure and recent studies have revealed that periodic table can be formulated using SO(4,2)* SU(2) group. IUPAC, the governing body in Chemistry, doesn't approve any periodic table as a standard...

HISTORY OF THE ORIGIN OF THE CHEMICAL ELEMENTS AND THEIR DISCOVERERS

International Nuclear Information System (INIS)

Holden, N.E.

2001-01-01

What do we mean by a chemical element? A chemical element is matter, all of whose atoms are alike in having the same positive charge on the nucleus and the same number of extra-nuclear electrons. As we shall see in the following elemental review, the origin of the chemical elements show a wide diversity with some of these elements having an origin in antiquity, other elements having been discovered within the past few hundred years and still others have been synthesized within the past fifty years via nuclear reactions on heavy elements since these other elements are unstable and radioactive and do not exist in nature

HISTORY OF THE ORIGIN OF THE CHEMICAL ELEMENTS AND THEIR DISCOVERIES.

Energy Technology Data Exchange (ETDEWEB)

HOLDEN,N.E.

2001-06-29

What do we mean by a chemical element? A chemical element is matter, all of whose atoms are alike in having the same positive charge on the nucleus and the same number of extra-nuclear electrons. As we shall see in the following elemental review, the origin of the chemical elements show a wide diversity with some of these elements having an origin in antiquity, other elements having been discovered within the past few hundred years and still others have been synthesized within the past fifty years via nuclear reactions on heavy elements since these other elements are unstable and radioactive and do not exist in nature.

The Need for Systematic Naming Software Tools for Exchange of Chemical Information

Directory of Open Access Journals (Sweden)

Andrey Yerin

1999-09-01

Full Text Available The availability of systematic names can enable the simple textual exchange of chemical structure information. The exchange of molecular structures in graphical format or connection tables has become well established in the field of cheminformatics and many structure drawing tools exist to enable this exchange. However, even with the availability of systematic naming rules, software tools to allow the generation of names from structures, and hopefully the reversal of these systematic names back to the original chemical structure, have been sorely lacking in capability and quality. Here we review the need for systematic naming as well as some of the tools and approaches being taken today in this area.

Statistic analysis of grouping in evaluation of the behavior of stable chemical elements and physical-chemical parameters in effluent from uranium mining; Analise de agrupamento na avaliacao do comportamento de elementos quimicos estaveis e parametros fisico-quimicos em efluente de mineracao de uranio

Energy Technology Data Exchange (ETDEWEB)

Pereira, Wagner de S., E-mail: wspereira@inb.gov.br, E-mail: pereirarsj@gmail.com [Universidade Federal Fluminense (GETA/LARARA-PLS/UFF), Niteroi, RJ (Brazil). Grupo de Estudos em Temas Ambientais. Laboratorio de Radiobiologia e Radiometria Pedro Lopes dos Santos; Py Junior, Delcy de A.; Dores, Luis A. de C.B.; Campelo, Emanuele L.C.; Morais, Gustavo F. de; Kelecom, Alphonse, E-mail: delcy@inb.gov.br, E-mail: kclecom@uol.com.br [lndustrias Nucleares do Brasil (UTM/INB), Pocos de Caldas, MG (Brazil). Unidade de Tratamento de Minerios; Pereira, Juliana R. de S., E-mail: pereirarsj@gmail.com [Universidade Federal de Alfenas, Pocos de Caldas, MG (Brazil)

2013-10-01

The Ore Treatment Unit (UTM) is a uranium mine off. The statistical analysis of clustering was used to evaluate the behavior of stable chemical elements and physico-chemical variables in their effluents. The use of cluster analysis proved effective in the evaluation, allowing to identify groups of chemical elements in physico-chemical variables and group analyzes (element and variables ). As a result, we can say, based on the analysis of the data, a strong link between Ca and Mg and between Al and TR{sub 2}O{sub 3} (rare earth oxides) in the UTM effluents. The SO{sub 4} was also identified as strongly linked to total solids and dissolved and these linked to electrical conductivity. Other associations existed, but were not as strongly linked. Additional collections for seasonal evaluation are required so that assessments can be confirmed. Additional statistics analysis (ordination techniques) should be used to help identify the origins of the groups identified in this analysis. (author)

Validation of new superheavy elements and IUPAC-IUPAP joint working group

International Nuclear Information System (INIS)

Jarlskog, Cecilia

2016-01-01

The great chemist Glenn Seaborg has written a delightful little book “Man-made Transuranium Elements”, published in 1963, in which he points out that: “The former basic criterion for the discovery of a new element – namely, chemical identification and separation from all previously-known elements – had to be changed in the case of lawrencium (element 103). This also may be true for elements beyond lawrencium.” Indeed this is what has happened. The elements with Z ≥ 103 are produced in nuclear reactions and are detected by counters. The detectors have undergone substantial refinement. For example one uses multiwire proportional chambers [for which George Charpak received the 1992 Nobel Prize in Physics] as well as solid state micro-strip detectors. In spite of this remarkable shift from chemistry to physics, the managerial staff of the International Union of Pure and Applied Chemistry (IUPAC) does not seem to be aware of what has been going on. The validation of superheavy elements should be done by physicists as the chemists lack the relevant competence as I will discuss here below. This article is about a collaboration between International Union of Pure and Applied Chemistry (IUPAC) and its sister organization International Union of Pure and Applied Physics (IUPAP), to deal with discovery of superheavy elements beyond Z = 112. I spent a great deal of time on this issue. In my opinion, the collaboration turned out to be a failure. For the sake of science, which should be our most important concern (and not politics), the rules for the future collaborations, if any, should be accurately defined and respected. The validation of new elements should be done by people who have the relevant competence – the physicists.

Chemistry of the superheavy elements.

Science.gov (United States)

Schädel, Matthias

2015-03-13

The quest for superheavy elements (SHEs) is driven by the desire to find and explore one of the extreme limits of existence of matter. These elements exist solely due to their nuclear shell stabilization. All 15 presently 'known' SHEs (11 are officially 'discovered' and named) up to element 118 are short-lived and are man-made atom-at-a-time in heavy ion induced nuclear reactions. They are identical to the transactinide elements located in the seventh period of the periodic table beginning with rutherfordium (element 104), dubnium (element 105) and seaborgium (element 106) in groups 4, 5 and 6, respectively. Their chemical properties are often surprising and unexpected from simple extrapolations. After hassium (element 108), chemistry has now reached copernicium (element 112) and flerovium (element 114). For the later ones, the focus is on questions of their metallic or possibly noble gas-like character originating from interplay of most pronounced relativistic effects and electron-shell effects. SHEs provide unique opportunities to get insights into the influence of strong relativistic effects on the atomic electrons and to probe 'relativistically' influenced chemical properties and the architecture of the periodic table at its farthest reach. In addition, they establish a test bench to challenge the validity and predictive power of modern fully relativistic quantum chemical models. © 2015 The Author(s) Published by the Royal Society. All rights reserved.

Piracicaba River Basin: evaluation of chemical elements in deep sediment profile by INAA

Energy Technology Data Exchange (ETDEWEB)

França, Elvis J. de; Santos, Robson A.; Santos, Katarine M. Barbosa; Silva, Gleyce K. A. [Centro Regional de Ciencias Nucleares do Nordeste (DIAMB/CRCN-NE/CNEN-PE), Recife, PE (Brazil). Div, de Monitoração Ambiental; Fernandes, Elisabete A. de Nadai; Rodrigues, Vanessa S.; Cavalca, Isabel P.O., E-mail: ejfranca@cnen.gov.br, E-mail: lis@cena.usp.br [Centro de Energia Nuclear na Agricultura (CENA/USP), Piracicaba, SP (Brazil)

2017-07-01

Many hydrographic basins have been impacted by anthropogenic sources, the Piracicaba River Basin of the State of São Paulo, is one of that. The total concentrations of chemical elements in deep sediments of basin may be indicate those available in ecosystem. Therefore, in this research concentration of chemical elements on deep sediment profile sampled of Piracicaba River Basin was determined by k0-Instrumental Neutron Activation Analysis. After collecting the 60 cm depth profile, samples were obtained by sectioning the sediment profile in 5 cm layers, totalizing 12 samples. Analytical portions were transferred to polyethylene vials for neutron irradiation at the Nuclear Research Reactor IEA-R1 from the Instituto de Pesquisas Energéticas e Nucleares IPEN/CNEN. After waiting for radiation safe levels, irradiated samples were transported to the Radioisotopes Laboratory from the Centro de Energia Nuclear na Agricultura CENA/USP. High Resolution Gamma-Ray Spectrometry using HPGe detectors was applied to measure the induced radioactivity. The chemical element mass fractions and their respective expanded analytical uncertainties (95% confidence level) were determined by k0-INAA using the in-house software Quantu. Geological reference materials were analyzed with samples to evaluate the quality of the analytical procedure. Results indicated the presence of enriched surface sediments (0-10 cm depth) for As, Ba, Ca, Co, Cs, Fe, Sb, Sc, Sr, Yb and Zn, despite no alteration was observed for Eu, Ta and Tb. Therefore, the evaluation of deep sediment profile afford the chemical element dynamics for the Piracicaba Basin. (author)

Piracicaba River Basin: evaluation of chemical elements in deep sediment profile by INAA

International Nuclear Information System (INIS)

França, Elvis J. de; Santos, Robson A.; Santos, Katarine M. Barbosa; Silva, Gleyce K. A.

2017-01-01

Many hydrographic basins have been impacted by anthropogenic sources, the Piracicaba River Basin of the State of São Paulo, is one of that. The total concentrations of chemical elements in deep sediments of basin may be indicate those available in ecosystem. Therefore, in this research concentration of chemical elements on deep sediment profile sampled of Piracicaba River Basin was determined by k0-Instrumental Neutron Activation Analysis. After collecting the 60 cm depth profile, samples were obtained by sectioning the sediment profile in 5 cm layers, totalizing 12 samples. Analytical portions were transferred to polyethylene vials for neutron irradiation at the Nuclear Research Reactor IEA-R1 from the Instituto de Pesquisas Energéticas e Nucleares IPEN/CNEN. After waiting for radiation safe levels, irradiated samples were transported to the Radioisotopes Laboratory from the Centro de Energia Nuclear na Agricultura CENA/USP. High Resolution Gamma-Ray Spectrometry using HPGe detectors was applied to measure the induced radioactivity. The chemical element mass fractions and their respective expanded analytical uncertainties (95% confidence level) were determined by k0-INAA using the in-house software Quantu. Geological reference materials were analyzed with samples to evaluate the quality of the analytical procedure. Results indicated the presence of enriched surface sediments (0-10 cm depth) for As, Ba, Ca, Co, Cs, Fe, Sb, Sc, Sr, Yb and Zn, despite no alteration was observed for Eu, Ta and Tb. Therefore, the evaluation of deep sediment profile afford the chemical element dynamics for the Piracicaba Basin. (author)

Carbon black vs. black carbon and other airborne materials containing elemental carbon: Physical and chemical distinctions

International Nuclear Information System (INIS)

Long, Christopher M.; Nascarella, Marc A.; Valberg, Peter A.

2013-01-01

Airborne particles containing elemental carbon (EC) are currently at the forefront of scientific and regulatory scrutiny, including black carbon, carbon black, and engineered carbon-based nanomaterials, e.g., carbon nanotubes, fullerenes, and graphene. Scientists and regulators sometimes group these EC-containing particles together, for example, interchangeably using the terms carbon black and black carbon despite one being a manufactured product with well-controlled properties and the other being an undesired, incomplete-combustion byproduct with diverse properties. In this critical review, we synthesize information on the contrasting properties of EC-containing particles in order to highlight significant differences that can affect hazard potential. We demonstrate why carbon black should not be considered a model particle representative of either combustion soots or engineered carbon-based nanomaterials. Overall, scientific studies need to distinguish these highly different EC-containing particles with care and precision so as to forestall unwarranted extrapolation of properties, hazard potential, and study conclusions from one material to another. -- Highlights: •Major classes of elemental carbon-containing particles have distinct properties. •Despite similar names, carbon black should not be confused with black carbon. •Carbon black is distinguished by a high EC content and well-controlled properties. •Black carbon particles are characterized by their heterogenous properties. •Carbon black is not a model particle representative of engineered nanomaterials. -- This review demonstrates the significant physical and chemical distinctions between elemental carbon-containing particles e.g., carbon black, black carbon, and engineered nanomaterials

Three Packets of Minerals of the Periodic Table of Chemical Elements and Chemical Compounds

OpenAIRE

Labushev, Mikhail M.

2013-01-01

The concepts of alpha- and beta-packets of the periodic table of chemical elements and chemical compounds are defined. The first of the 47 minerals alpha-packets is composed. In it all minerals are arranged in increasing Iav index of proportionality of atomic weights of composing chemical elements, the same way as chemical elements are located in increasing atomic weights in the Periodic table. The packet includes 93 known minerals and two compounds - N2O5 and CO2 - being actually minerals. B...

Measurements of radon and chemical elements: Popocatepetl volcano

International Nuclear Information System (INIS)

Pena, P.; Segovia, N.; Lopez, B.; Reyes, A.V.; Armienta, M.A.; Valdes, C.; Mena, M.; Seidel, J.L.; Monnin, M.

2002-01-01

The Popocatepetl volcano is a higher risk volcano located at 60 Km from Mexico City. Radon measurements on soil in two fixed seasons located in the north slope of volcano were carried out. Moreover the radon content, major chemical elements and tracks in water samples of three springs was studied. The radon of soil was determined with solid detectors of nuclear tracks (DSTN). The radon in subterranean water was evaluated through the liquid scintillation method and it was corroborated with an Alpha Guard equipment. The major chemical elements were determined with conventional chemical methods and the track elements were measured using an Icp-Ms equipment. The radon on soil levels were lower, indicating a moderate diffusion of the gas across the slope of the volcano. The radon in subterranean water shown few changes in relation with the active scene of the volcano. The major chemical elements and tracks showed a stable behavior during the sampling period. (Author)

Ion-selective electrodes in organic elemental and functional group analysis: a review

Energy Technology Data Exchange (ETDEWEB)

Selig, W.

1977-11-08

The literature on the use of ion-selective electrodes in organic elemental and functional group analysis is surveyed in some detail. The survey is complete through Chemical Abstracts, Vol. 83 (1975). 40 figures, 52 tables, 236 references.

Ion-selective electrodes in organic elemental and functional group analysis: a review

International Nuclear Information System (INIS)

Selig, W.

1977-01-01

The literature on the use of ion-selective electrodes in organic elemental and functional group analysis is surveyed in some detail. The survey is complete through Chemical Abstracts, Vol. 83 (1975). 40 figures, 52 tables, 236 references

Cumulative and competitive effects of chemical elements on nuclear glass alteration

International Nuclear Information System (INIS)

Arena, Helene

2016-01-01

This work takes place in the context of the long-term behavior of nuclear glasses under repository conditions. The main objective is to identify, understand and compare the effects of some chemical elements present in the glass composition and/or in the repository media (Zn, Mg, Ni, Co, Fe, Ca, Gd, Ce, K, Cs, Cr and Ag) on the processes involved in glass alteration by water. The cumulative or competitive nature of the effects of these chemical elements was determined. To reach this goal, a 6 oxides simple glass (ISG) has been altered for more than 500 days in a solution containing one or more of the chemical elements of interest. The results indicate that Zn, Mg, Ni, Co and Fe elements increase glass alteration forming secondary phases with the same structure and stoichiometry (tri-octahedral smectites). To form, these silicates consume chemical elements (Si, Al) from the environment and induce a pH decrease until a limiting value of pH. Beyond this pH the precipitation of secondary phases is inhibited and these chemical elements can be integrated into the gel, replacing Ca whose solubility increases at lower pH. As long as they form secondary phases, the effects of these elements are cumulative. Rare earths Gd and Ce also increase glass alteration forming secondary phases but their effects are lower as they contain less silicon. These elements are not integrated in the gel. Chromium increases glass alteration by precipitating with Ca and leading to a less protective gel, depleted in Ca. Silver precipitates as AgCl and has no effect on the alteration of the glass. The chemical elements K, Cs and Ca limit glass alteration by integrating into the gel and slowing down the transport phenomena therein. This integration is competitive: the order of integration (quantity and effectiveness glass alteration limitation) is the following Ca≥≥Cs≥K. Thus, the increase of glass alteration may be proportional to the quantity of elements promoting the precipitation of

Element 74, the Wolfram Versus Tungsten Controversy

Energy Technology Data Exchange (ETDEWEB)

Holden,N.E.

2008-08-11

Two and a quarter centuries ago, a heavy mineral ore was found which was thought to contain a new chemical element called heavy stone (or tungsten in Swedish). A few years later, the metal was separated from its oxide and the new element (Z=74) was called wolfram. Over the years since that time, both the names wolfram and tungsten were attached to this element in various countries. Sixty years ago, IUPAC chose wolfram as the official name for the element. A few years later, under pressure from the press in the USA, the alternative name tungsten was also allowed by IUPAC. Now the original, official name 'wolfram' has been deleted by IUPAC as one of the two alternate names for the element. The history of this controversy is described here.

EDXRF applied to the chemical element determination of small invertebrate samples

International Nuclear Information System (INIS)

Magalhaes, Marcelo L.R.; Santos, Mariana L.O.; Cantinha, Rebeca S.; Souza, Thomas Marques de; Franca, Elvis J. de

2015-01-01

Energy Dispersion X-Ray Fluorescence - EDXRF is a fast analytical technique of easy operation, however demanding reliable analytical curves due to the intrinsic matrix dependence and interference during the analysis. By using biological materials of diverse matrices, multielemental analytical protocols can be implemented and a group of chemical elements could be determined in diverse biological matrices depending on the chemical element concentration. Particularly for invertebrates, EDXRF presents some advantages associated to the possibility of the analysis of small size samples, in which a collimator can be used that directing the incidence of X-rays to a small surface of the analyzed samples. In this work, EDXRF was applied to determine Cl, Fe, P, S and Zn in invertebrate samples using the collimator of 3 mm and 10 mm. For the assessment of the analytical protocol, the SRM 2976 Trace Elements in Mollusk produced and SRM 8415 Whole Egg Powder by the National Institute of Standards and Technology - NIST were also analyzed. After sampling by using pitfall traps, invertebrate were lyophilized, milled and transferred to polyethylene vials covered by XRF polyethylene. Analyses were performed at atmosphere lower than 30 Pa, varying voltage and electric current according to the chemical element to be analyzed. For comparison, Zn in the invertebrate material was also quantified by graphite furnace atomic absorption spectrometry after acid treatment (mixture of nitric acid and hydrogen peroxide) of samples have. Compared to the collimator of 10 mm, the SRM 2976 and SRM 8415 results obtained by the 3 mm collimator agreed well at the 95% confidence level since the E n Number were in the range of -1 and 1. Results from GFAAS were in accordance to the EDXRF values for composite samples. Therefore, determination of some chemical elements by EDXRF can be recommended for very small invertebrate samples (lower than 100 mg) with advantage of preserving the samples. (author)

Origin of the chemical elements

Energy Technology Data Exchange (ETDEWEB)

Tayler, R J

1984-05-01

The subject is discussed in relation to the composition of initially created matter and changes which have occurred during the life history of the universe, with particular reference to our galaxy and nearby galaxies. Headings are: observations of element abundances (stars, gas clouds in our own and nearby galaxies, hot gas in galaxy clusters, the solar system); the originally created matter (Big Bang theory and early nuclear reactions); processes changing observed composition (galactic evolution; nuclear fusion reactions in stellar interiors; chemical composition of a highly evolved massive star); supernovae (production of heavy elements); chemical evolution of the galaxy; production of very heavy elements (s process, r process).

The periodic system of chemical elements: old and new developments

International Nuclear Information System (INIS)

Kibler, M.

1987-09-01

Some historical facts about the construction of a periodic system of chemical elements are reviewed. The Madelung rule is used to generate an unusual format for the periodic table. Following the work of Byakov, Kulakov, Rumer and Fet, such a format is further refined on the basis of a chain of groups starting with SU(2)xS0(4.2)

Dataset on elemental concentration and group identification of ancient potteries from Tamil Nadu, India

Directory of Open Access Journals (Sweden)

A. Chandrasekaran

2017-02-01

Full Text Available The dataset contains concentration of major and trace elements of ancient potteries from Tamilnadu and grouping different potteries from the statistical techniques of factor and cluster analysis (Figs. 2, 3 and 4. The major and trace elemental concentration data generated using energy dispersive X-ray fluorescence technique (EDXRF and factor and cluster analysis data obtained using STATISTICA (10.0 version software. The concentration of major and trace elements determines the type of clay minerals (Calcareous/Non-Calcareous and either low or high refractory and firing atmosphere adopted by the artisans at the time of manufacture. The statistical tool examined graphically the grouping pattern of the samples in terms of chemical composition and extract information about their provenance. The compilation of this data provides a resource for the wider research community in archeology.

Exploring the Everyday Context of Chemical Elements: Discovering the Elements of Car Components

Science.gov (United States)

Franco-Mariscal, Antonio Joaquín

2015-01-01

This paper presents a project about the chemical elements made by 15-year-old Spanish high school students of Chemistry. It focuses on context-based teaching combined with the advantages of creating a large mural which subsequently is exposed in the school. The project consisted of researching the chemical elements in the different materials that…

Present status of research activities conducted by research group for heavy elements microbiology in JAERI

International Nuclear Information System (INIS)

Ohnuki, Toshihiko; Ozaki, Takuo; Yoshida, Takahiro

2004-01-01

It has been recognized that microbial transformations of radionuclides and toxic metals could be significant in the environment, but there is a paucity of information on the mechanisms of biotransformation of radionuclides by the microorganisms. An understanding at the fundamental level the mechanisms of mobilization, immobilization and bioavailability of radioactive elements in particular the actinides is important from the standpoint of mobility of actinides in the environment, disposal of radioactive wastes in deep geological formation, remediation of contaminated soils and materials, and development of strategies for the long-term stewardship of the contaminated sites. The microbiology research group in Japan Atomic Energy Research Institute (JAERI) is conducting basic scientific research on microbial interactions with actinides. Fundamental research on microbial transformations of actinides include elucidation of the mechanisms of dissolution and precipitation of various chemical forms such as ionic, oxides, organic and inorganic complexes of actinides by aerobic or anaerobic microorganisms under relevant microbial process conditions. State-of-the-art analytical techniques are used to determine the interaction of actinides with microorganisms at the molecular level to understand the structure function relationship. These techniques include time-resolved laser fluorescence spectroscopy (TRLFS) to determine the coordination number, oxidation states and the nearest neighbor by X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) at the Synchrotron Light Source, identification of functional groups by nuclear magnetic resonance (NMR), determination of chemical forms by transmission electron microscopy (TEM), and genomic (DNA) manipulation by molecular techniques. We here report the present status of our research activities on accumulation of lanthanides(III) by microorganisms, application of micro-particle induced X

Chemical experiments with superheavy elements.

Science.gov (United States)

Türler, Andreas

2010-01-01

Unnoticed by many chemists, the Periodic Table of the Elements has been extended significantly in the last couple of years and the 7th period has very recently been completed with eka-Rn (element 118) currently being the heaviest element whose synthesis has been reported. These 'superheavy' elements (also called transactinides with atomic number > or = 104 (Rf)) have been artificially synthesized in fusion reactions at accelerators in minute quantities of a few single atoms. In addition, all isotopes of the transactinide elements are radioactive and decay with rather short half-lives. Nevertheless, it has been possible in some cases to investigate experimentally chemical properties of transactinide elements and even synthesize simple compounds. The experimental investigation of superheavy elements is especially intriguing, since theoretical calculations predict significant deviations from periodic trends due to the influence of strong relativistic effects. In this contribution first experiments with hassium (Hs, atomic number 108), copernicium (Cn, atomic number 112) and element 114 (eka-Pb) are reviewed.

Chemical Abundance Analysis of Moving Group W11450 (Latham 1)

Science.gov (United States)

O'Connell, Julia E.; Martens, Kylee; Frinchaboy, Peter M.

2016-12-01

We present elemental abundances for all seven stars in Moving Group W11450 (Latham 1) to determine if they may be chemically related. These stars appear to be both spatially and kinematically related, but no spectroscopic abundance analysis exists in literature. Abundances for eight elements were derived via equivalent width analyses of high-resolution (R ˜ 60,000), high-signal-to-noise ratio ( ˜ 100) spectra obtained with the Otto Struve 2.1 m telescope and the Sandiford Echelle Spectrograph at McDonald Observatory. The large star-to-star scatter in metallicity, -0.55 ≤ [Fe/H] ≤slant 0.06 dex (σ = 0.25), implies these stars were not produced from the same chemically homogeneous molecular cloud, and are therefore not part of a remnant or open cluster as previously proposed. Prior to this analysis, it was suggested that two stars in the group, W11449 and W11450, are possible wide binaries. The candidate wide binary pair show similar chemical abundance patterns with not only iron but with other elements analyzed in this study, suggesting the proposed connection between these two stars may be real.

Uptake of traffic-related heavy metals and platinum group elements (PGE) by plants

Energy Technology Data Exchange (ETDEWEB)

Schaefer, J.; Hannker, D.; Eckhardt, J.D.; Stueben, D. [Institute of Petrography and Geochemistry, University of Karlsruhe, Karlsruhe (Germany)

1998-04-23

The distribution of the platinum group elements (PGE) caused by traffic emissions from autoexhaust catalysts has been determined in soils and different types of plants. The plants (spinach, cress, phacelia, stinging nettle) were cultivated on different soils collected from areas adjacent to a German highway and on uncontaminated sandy and clayey soils. The main result of the experiments was a measurable transfer of PGE from contaminated soil to plants. Following the definition of Sauerbeck (Beurteilung von Schwermetallkontaminationen im Boden. Frankfurt/Main: Dechema-Fachgespraeche, 1989:281-316), Pt, Rh and Pd transfer coefficients are within the range of immobile to moderately mobile elements, such as Cu. The transfer coefficient decreases from Pd>Pt{>=}Rh. Palladium therefore is the most biologically available of this element group

Electronic Transmutation (ET): Chemically Turning One Element into Another.

Science.gov (United States)

Zhang, Xinxing; Lundell, Katie A; Olson, Jared K; Bowen, Kit H; Boldyrev, Alexander I

2018-03-08

The concept of electronic transmutation (ET) depicts the processes that by acquiring an extra electron, an element with the atomic number Z begins to have properties that were known to only belong to its neighboring element with the atomic number Z+1. Based on ET, signature compounds and chemical bonds that are composed of certain elements can now be designed and formed by other electronically transmutated elements. This Minireview summarizes the recent developments and applications of ET on both the theoretical and experimental fronts. Examples on the ET of Group 13 elements into Group 14 elements, Group 14 elements into Group 15 elements, and Group 15 elements into Group 16 elements are discussed. Compounds and chemical bonding composed of carbon, silicon, germanium, phosphorous, oxygen and sulfur now have analogues using transmutated boron, aluminum, gallium, silicon, nitrogen, and phosphorous. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Accumulation of platinum group elements by the marine gastropod Littorina littorea

Energy Technology Data Exchange (ETDEWEB)

Mulholland, Rachel [School of Geography, Earth and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom); Turner, Andrew, E-mail: aturner@plymouth.ac.uk [School of Geography, Earth and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom)

2011-04-15

The accumulation and trophic transfer of the platinum group elements (PGE): Rh, Pd and Pt; have been studied in short-term (5 day) exposures conducted in aquaria containing the marine macroalga, Ulva lactuca, and/or the grazing mollusc, Littorina littorea. Metals added to sea water (to concentrations of 20 {mu}g L{sup -1}) were taken up by U. lactuca in the order Rh, Pt > Pd and by L. littorea in the order Pd {>=} Pt {>=} Rh, with greatest metal accumulation in the latter generally occurring in the visceral complex and kidney. When fed contaminated alga, accumulation of Rh and Pd by L. littorea, relative to total available metal, increased by an order of magnitude, while accumulation of Pt was not readily detected. We conclude that the diet is the most important vector for accumulation of Rh and Pd, while accumulation of Pt appears to proceed mainly from the aqueous phase. - Research highlights: > Platinum group elements are accumulated by, Littorina littorea. > The aqueous phase and diet are important vehicles for Rh and Pd accumulation by the snail. > Grazing molluscs may serve as biomonitors of coastal PGE contamination. - Platinum group elements are accumulated by the marine snail, Littorina littorea, from both the aqueous phase and the diet.

EDXRF applied to the chemical element determination of small invertebrate samples

Energy Technology Data Exchange (ETDEWEB)

Magalhaes, Marcelo L.R.; Santos, Mariana L.O.; Cantinha, Rebeca S.; Souza, Thomas Marques de; Franca, Elvis J. de, E-mail: marcelo_rlm@hotmail.com, E-mail: marianasantos_ufpe@hotmail.com, E-mail: rebecanuclear@gmail.com, E-mail: thomasmarques@live.com.pt, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

2015-07-01

Energy Dispersion X-Ray Fluorescence - EDXRF is a fast analytical technique of easy operation, however demanding reliable analytical curves due to the intrinsic matrix dependence and interference during the analysis. By using biological materials of diverse matrices, multielemental analytical protocols can be implemented and a group of chemical elements could be determined in diverse biological matrices depending on the chemical element concentration. Particularly for invertebrates, EDXRF presents some advantages associated to the possibility of the analysis of small size samples, in which a collimator can be used that directing the incidence of X-rays to a small surface of the analyzed samples. In this work, EDXRF was applied to determine Cl, Fe, P, S and Zn in invertebrate samples using the collimator of 3 mm and 10 mm. For the assessment of the analytical protocol, the SRM 2976 Trace Elements in Mollusk produced and SRM 8415 Whole Egg Powder by the National Institute of Standards and Technology - NIST were also analyzed. After sampling by using pitfall traps, invertebrate were lyophilized, milled and transferred to polyethylene vials covered by XRF polyethylene. Analyses were performed at atmosphere lower than 30 Pa, varying voltage and electric current according to the chemical element to be analyzed. For comparison, Zn in the invertebrate material was also quantified by graphite furnace atomic absorption spectrometry after acid treatment (mixture of nitric acid and hydrogen peroxide) of samples have. Compared to the collimator of 10 mm, the SRM 2976 and SRM 8415 results obtained by the 3 mm collimator agreed well at the 95% confidence level since the E{sub n} Number were in the range of -1 and 1. Results from GFAAS were in accordance to the EDXRF values for composite samples. Therefore, determination of some chemical elements by EDXRF can be recommended for very small invertebrate samples (lower than 100 mg) with advantage of preserving the samples. (author)

Gesture and naming therapy for people with severe aphasia: a group study.

Science.gov (United States)

Marshall, Jane; Best, Wendy; Cocks, Naomi; Cruice, Madeline; Pring, Tim; Bulcock, Gemma; Creek, Gemma; Eales, Nancy; Mummery, Alice Lockhart; Matthews, Niina; Caute, Anna

2012-06-01

In this study, the authors (a) investigated whether a group of people with severe aphasia could learn a vocabulary of pantomime gestures through therapy and (b) compared their learning of gestures with their learning of words. The authors also examined whether gesture therapy cued word production and whether naming therapy cued gestures. Fourteen people with severe aphasia received 15 hr of gesture and naming treatments. Evaluations comprised repeated measures of gesture and word production, comparing treated and untreated items. Baseline measures were stable but improved significantly following therapy. Across the group, improvements in naming were greater than improvements in gesture. This trend was evident in most individuals' results, although 3 participants made better progress in gesture. Gains were item specific, and there was no evidence of cross-modality cueing. Items that received gesture therapy did not improve in naming, and items that received naming therapy did not improve in gesture. Results show that people with severe aphasia can respond to gesture and naming therapies. Given the unequal gains, naming may be a more productive therapy target than gesture for many (although not all) individuals with severe aphasia. The communicative benefits of therapy were not examined but are addressed in a follow-up article.

Mineralogy of the rare earth elements

International Nuclear Information System (INIS)

Clark, A.M.

1984-01-01

This paper contains mineralogic properties of the rare earth elements (REE). Notes are given on total REE abundances, distribution patterns, and modes of occurrence. References are confined as far as possible to papers containing usable REE data. The minerals are grouped alphabetically within each major cationic group. The paper includes an alphabetic table of mineral names, chemical formulas, crystal system and section number. It functions as a handy entrance to the mineralogic and bibliographic paper. (G.J.P.)

Enhancing of chemical compound and drug name recognition using representative tag scheme and fine-grained tokenization.

Science.gov (United States)

Dai, Hong-Jie; Lai, Po-Ting; Chang, Yung-Chun; Tsai, Richard Tzong-Han

2015-01-01

The functions of chemical compounds and drugs that affect biological processes and their particular effect on the onset and treatment of diseases have attracted increasing interest with the advancement of research in the life sciences. To extract knowledge from the extensive literatures on such compounds and drugs, the organizers of BioCreative IV administered the CHEMical Compound and Drug Named Entity Recognition (CHEMDNER) task to establish a standard dataset for evaluating state-of-the-art chemical entity recognition methods. This study introduces the approach of our CHEMDNER system. Instead of emphasizing the development of novel feature sets for machine learning, this study investigates the effect of various tag schemes on the recognition of the names of chemicals and drugs by using conditional random fields. Experiments were conducted using combinations of different tokenization strategies and tag schemes to investigate the effects of tag set selection and tokenization method on the CHEMDNER task. This study presents the performance of CHEMDNER of three more representative tag schemes-IOBE, IOBES, and IOB12E-when applied to a widely utilized IOB tag set and combined with the coarse-/fine-grained tokenization methods. The experimental results thus reveal that the fine-grained tokenization strategy performance best in terms of precision, recall and F-scores when the IOBES tag set was utilized. The IOBES model with fine-grained tokenization yielded the best-F-scores in the six chemical entity categories other than the "Multiple" entity category. Nonetheless, no significant improvement was observed when a more representative tag schemes was used with the coarse or fine-grained tokenization rules. The best F-scores that were achieved using the developed system on the test dataset of the CHEMDNER task were 0.833 and 0.815 for the chemical documents indexing and the chemical entity mention recognition tasks, respectively. The results herein highlight the importance

Adaptive Finite Element Method Assisted by Stochastic Simulation of Chemical Systems

KAUST Repository

Cotter, Simon L.; Vejchodský , Tomá š; Erban, Radek

2013-01-01

Stochastic models of chemical systems are often analyzed by solving the corresponding Fokker-Planck equation, which is a drift-diffusion partial differential equation for the probability distribution function. Efficient numerical solution of the Fokker-Planck equation requires adaptive mesh refinements. In this paper, we present a mesh refinement approach which makes use of a stochastic simulation of the underlying chemical system. By observing the stochastic trajectory for a relatively short amount of time, the areas of the state space with nonnegligible probability density are identified. By refining the finite element mesh in these areas, and coarsening elsewhere, a suitable mesh is constructed and used for the computation of the stationary probability density. Numerical examples demonstrate that the presented method is competitive with existing a posteriori methods. © 2013 Society for Industrial and Applied Mathematics.

The origin of the chemical elements

International Nuclear Information System (INIS)

Tayler, R.J.

1984-01-01

The subject is discussed in relation to the composition of initially created matter and changes which have occurred during the life history of the universe, with particular reference to our galaxy and nearby galaxies. Headings are: observations of element abundances (stars, gas clouds in our own and nearby galaxies, hot gas in galaxy clusters, the solar system); the originally created matter (Big Bang theory and early nuclear reactions); processes changing observed composition (galactic evolution; nuclear fusion reactions in stellar interiors; chemical composition of a highly evolved massive star); supernovae (production of heavy elements); chemical evolution of the galaxy; production of very heavy elements (s process, r process). (U.K.)

Content of Chemical Elements in Wood-Destroying Fungi

Directory of Open Access Journals (Sweden)

Strapáč I.

2016-12-01

Full Text Available The aim of this study was to examine the content of chemical elements in the dried fruiting bodies of edible wood decaying fungi such as Honey mushrooms (Armillaria mellea, Shiitakes (Lentinus edodes and Oyster mushrooms (Pleurotus ostreatus. Powdered samples of fungi were mineralized in a microwave digestion. Twenty-one (21 chemical elements were detected in the plasma of the device ICP-MS AGILENT 7500c by accredited methods with the aid of calibration curves. The content of individual elements varied within a considerable range. The highest contents of K, Mn, Cu and Cd were found in the fruiting bodies of Honey mushrooms (Armillaria mellea. Shiitakes (Lentinus edodes had the highest content of B and Mo. Significant differences were found in the content of elements in the Oyster mushrooms (Pleurotus ostreatus from Slovakia, Hungary and China. The highest content of Al was found in the Oyster mushrooms (Pleurotus ostreatus from Hungary. The Chinese oysters had a maximum contents of Ca, Mg, Co, Pb, As and U. The Oyster mushrooms (Pleurotus ostreatus from Lemešany (Slovakia had the highest contents of Na, Zn, Fe, Se, Ag, Hg and Cr. The difference of chemical element content could be influenced by the genotype of the fungus and by the composition of substrate on which mushroom grow up.

Chemical functionalization and edge doping of zigzag graphene nanoribbon with L-(+)-leucine and group IB elements-A DFT study

Science.gov (United States)

Janani, K.; John Thiruvadigal, D.

2017-10-01

First-principles based density functional theory (DFT) calculations have been carried out on the chemically functionalized pure and Cu, Ag and Au doped zigzag graphene nanoribbon (ZGNR(6,0)) with the use of the branched chain amino acid L-(+)-Leucine named as LLZGNR(6,0), LLCuZGNR(6,0), LLAgZGNR(6,0) and LLAuZGNR(6,0) respectively. The structural stability for minimum total energy was confirmed by perturbating the geometry of the relaxed structures. The physical and chemical properties, such as band gap, chemical potential, transmission spectrum, charge transfer, bonding character and Gibb's free energy of solvation were analysed for all the four systems. It has been observed that the edge doping assisted functionalized systems (LLCuZGNR(6,0), LLAgZGNR(6,0) and LLAuZGNR(6,0)) without the inclusion of spin polarisation are semiconducting in nature. Whereas, barely functionalized system is found to be semi-metallic. An effective space charge polarisation in functionalized graphene nanoribbon has been revealed through charge transfer studies. Hence, it signifies the effective solubility of the nanoribbon in aqueous media. The results indicate the possibility of using such system as nanocarriers in targeted drug delivery applications.

Purposeful synthesis of chemical elements and ecologically pure mobile sources of energy

International Nuclear Information System (INIS)

Krivitsky, V. A.; Gareev, F. A.

2007-01-01

It is well known [1] that the natural geo-transmutation of chemical elements occurs in the atmosphere and earth in the regions of a strong change in geo-, bio-, acoustic-, and electromagnetic fields. The mineral row materials contain the same accompanying chemical combinations which are independent of mineral deposit [2]. This means that the formation of chemical elements occurs in the same physical and chemical conditions. These conditions were simulated on the fundamental cooperative resonance synchronization principle [1]. The experimental facility was constructed on the basis of our model which provided with the calculated final chemical elements. These experimental results indicate new possibilities for, simulating, inducing and controlling nuclear reactions by low energy external fields. The borrowing from the geo-transmutation mechanisms of chemical elements creates the fundamental directions in low energy nuclear reaction researches for construction of new ecologically pure mobile sources of energy independent of oil, gas and coal, new substances, and technologies. References [1] F.A. Gareev, I.E. Zhidkova, E-print arXiv Nucl-th/0610002 2006. [2] V.A. Krivzskii, Transmutazija ximicheskix elementov v evolyuzii Semli (in Russian), Moscow 2003

Pyrometallurgical partitioning of uranium and transuranic elements from rare earth elements by electrorefining and reductive extraction

International Nuclear Information System (INIS)

Uozumi, Koichi; Kinoshita, Kensuke; Inoue, Tadashi; Storvick, T.S.; Krueger, C.L.; Nabelek, C.R.

2001-01-01

High-level liquid waste generated from PUREX reprocessing contains a small amount of transuranic elements, such as Np, Pu, Am, and Cm, with long-lived radioactivities. A pyrometallurgical partitioning process is being developed to recover transuranic elements from such waste. Small amounts of U contained in the high-level liquid waste are also recovered in the process. A key issue for developing the process is effective separation of U and the transuranic elements from the rare-earth elements, because the two elemental groups are chemically analogous. A series of process tests were carried out in the present study to demonstrate that a combination of electrorefining and reductive extraction is useful for separating U and transuranic elements from the rare-earth elements. The results indicate that 99% of U and each transuranic elements is recovered by the combination process as a product, and that the quantity of rare-earth elements contained in the product is smaller than the transuranic elements by weight. The overall mass balance of U and transuranic elements in the system ranged within the experimental errors assigned to sampling and analysis. (author)

Several nomenclatural clarifications on genus-group names in the Aphididae (Hemiptera Sternorrhyncha)

Science.gov (United States)

The aphidologists attending the Eighth International Symposium on Aphids, held in Fremantle (Western Australia, 2005), charged us with the preparation of a Part of the List of Available Names in Zoology devoted to the aphid genus-group names. Our work was greatly facilitated by reference to the list...

Advances in chemical investigations of the heaviest elements

Directory of Open Access Journals (Sweden)

Türler Andreas

2016-01-01

Full Text Available Although somewhat in the shadow of the discoveries of new elements, experimental chemical investigations of the heaviest elements have made tremendous progress in the last decades. Indeed, it was possible to experimentally determine thermochemical properties of heavy transactinide elements such as copernicium or flerovium. But will it be possible to chemically study all currently known elements of the periodic table up to element 118? While it is experimentally feasible to work with single atoms, the short half-lives of even the longest currently known isotopes of elements 115 through 118 call for new experimental approaches.

Pesticides, selected elements, and other chemicals in adult total diet samples October 1979-September 1980

International Nuclear Information System (INIS)

Gartrell, M.J.; Craun, J.C.; Podrebarac, D.S.; Gunderson, E.L.

1985-01-01

The US Food and Drug Administration (FDA) conducts Total Diet Studies to determine the dietary intake of selected pesticides, industrial chemicals, and elements (including radionuclides). These studies involve the retail purchase and analysis of foods representative of the diets of infants, toddlers, and adults. The individual food items are separated into a number of food groups, each of which is analyzed as a composite. This report summarizes the results for adult Total Diet samples collected in 20 cities between October 1979 and September 1980. The average concentration, range of concentrations, and calculated average daily intake of each chemical found are presented by food group. The average daily intakes of the chemicals are similar to those found in the several preceding years and are within acceptable limits. The results for samples collected during the same period that represent the diets of infants and toddlers are reported separately

Plants' essential chemical elements

Science.gov (United States)

Kevin T. Smith

2007-01-01

Every garden center and hardware store sells fertilizer guaranteed to "feed" plants. In a strict sense, we can't feed plants. Food contains an energy source. Green plants capture solar energy and make their own food through photosynthesis! Photosynthesis and other metabolic processes require chemical elements in appropriate doses for plants to survive...

Chemical element abundance in K giant atmospheres

International Nuclear Information System (INIS)

Komarov, N.S.; Shcherbak, A.N.

1980-01-01

With the help of modified method of differential curves of growth studied are physical parameters of atmospheres of giant stars of KO111 spectral class of the NGC 752, M25 and UMa cluster. Observations have been made on reflector of Crimea astrophysical observatory of Academy of Sciences of the USSR in the period from February to May, 1978. Spectograms are obtained for the wave length range from 5000-5500 A. It is shown that the change of chemical content in the wide range in heavy element composition does not influence the star atmosphere structUre. It follows from the results of the investigation that the abundance of chemical elements in stars of various scattered clusters, is the same in the range of errors of measurements and is similar to the abundance of chemical elements in the Sun atmosphere

Multi trace element analysis of dry biological materials by neutron activation analysis including a chemical group separation

International Nuclear Information System (INIS)

Weers, C.A.

1980-01-01

The principles of activation analysis and the practical aspects of neutron activation analysis are outlined. The limits which are set to accuracy and precision are defined. The description of the evaporation process is summarised in terms of the half-volume. This quantity is then used to define the resolving power. The formulation is checked by radiotracer experiments. Dried animal blood is used as the testing material. The pretreatment of the samples and (the development of) the destruction-evaporation apparatus is described. Four successive devices were built and tested. The development of the successive adsorption steps with active charcoal, Al 2 O 3 and coprecipitation with Fe(OH) 3 is presented. Seven groups of about 25 elements in total can be determined this way. The results obtained for standard reference materials are summarized and compared with literature data. (Auth.)

EDXRF for determination of chemical elements in the beetle Alphitobius diaperinus

International Nuclear Information System (INIS)

Cantinha, Rebeca S.; Farias, Emerson E.G. de; Magalhaes, Marcelo L.R. de; Franca, Elvis J. de; Cunha, Franklin M. da; Zacarias, Vyvyane L.

2015-01-01

Energy Dispersion X-Ray Fluorescence (EDXRF) spectrometry has been widely employed for chemical element determination of biological matrices, including insects. The beetle Alphitobius diaperinus is a major problem in poultry production, thereby infesting poultry litter and stored grains. Up to now, little is known about the behavior, physiology and environmental interactions of this insect. In this paper, EDXRF was applied to quantify the main chemical elements in A. diaperinus. For the quality of the analytical protocol, certified reference materials produced by National Institute of Standards and Technology - NIST were analyzed together with the samples. The technique was able to quantify Cl, P, S and Zn in this insect, presenting no significant variation at the 95% confidence level among the repetitions (n = 4). A different pattern of chemical element accumulation in this beetle was noticed compared to other Coleoptera species, in which the concentration of the chemical elements were markedly lower in A. diaperinus, probably associated to the restricted availability of chemical elements in food. Since no result has been found in the literature before, A. diaperinus was firstly chemically characterized in this paper. (author)

EDXRF for determination of chemical elements in the beetle Alphitobius diaperinus

Energy Technology Data Exchange (ETDEWEB)

Cantinha, Rebeca S.; Farias, Emerson E.G. de; Magalhaes, Marcelo L.R. de; Franca, Elvis J. de, E-mail: rebecanuclear@gmail.com, E-mail: emersonemiliano@yahoo.com.br, E-mail: marcelo_rlm@hotmail.com, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Cunha, Franklin M. da; Zacarias, Vyvyane L., E-mail: ukento@yahoo.com.br, E-mail: vyvyanebiologicas@gmail.com [Universidade Federal Rural de Pernambuco (UFRPE), Recife, PE (Brazil)

2015-07-01

Energy Dispersion X-Ray Fluorescence (EDXRF) spectrometry has been widely employed for chemical element determination of biological matrices, including insects. The beetle Alphitobius diaperinus is a major problem in poultry production, thereby infesting poultry litter and stored grains. Up to now, little is known about the behavior, physiology and environmental interactions of this insect. In this paper, EDXRF was applied to quantify the main chemical elements in A. diaperinus. For the quality of the analytical protocol, certified reference materials produced by National Institute of Standards and Technology - NIST were analyzed together with the samples. The technique was able to quantify Cl, P, S and Zn in this insect, presenting no significant variation at the 95% confidence level among the repetitions (n = 4). A different pattern of chemical element accumulation in this beetle was noticed compared to other Coleoptera species, in which the concentration of the chemical elements were markedly lower in A. diaperinus, probably associated to the restricted availability of chemical elements in food. Since no result has been found in the literature before, A. diaperinus was firstly chemically characterized in this paper. (author)

Structure and magnetism in novel group IV element-based magnetic materials

Energy Technology Data Exchange (ETDEWEB)

Tsui, Frank [Univ. of North Carolina, Chapel Hill, NC (United States)

2013-08-14

The project is to investigate structure, magnetism and spin dependent states of novel group IV element-based magnetic thin films and heterostructures as a function of composition and epitaxial constraints. The materials systems of interest are Si-compatible epitaxial films and heterostructures of Si/Ge-based magnetic ternary alloys grown by non-equilibrium molecular beam epitaxy (MBE) techniques, specifically doped magnetic semiconductors (DMS) and half-metallic Heusler alloys. Systematic structural, chemical, magnetic, and electrical measurements are carried out, using x-ray microbeam techniques, magnetotunneling spectroscopy and microscopy, and magnetotransport. The work is aimed at elucidating the nature and interplay between structure, chemical order, magnetism, and spin-dependent states in these novel materials, at developing materials and techniques to realize and control fully spin polarized states, and at exploring fundamental processes that stabilize the epitaxial magnetic nanostructures and control the electronic and magnetic states in these complex materials. Combinatorial approach provides the means for the systematic studies, and the complex nature of the work necessitates this approach.

Chemical Differentiation of Osseous, Dental, and Non-skeletal Materials in Forensic Anthropology using Elemental Analysis.

Science.gov (United States)

Zimmerman, Heather A; Meizel-Lambert, Cayli J; Schultz, John J; Sigman, Michael E

2015-03-01

Forensic anthropologists are generally able to identify skeletal materials (bone and tooth) using gross anatomical features; however, highly fragmented or taphonomically altered materials may be problematic to identify. Several chemical analysis techniques have been shown to be reliable laboratory methods that can be used to determine if questionable fragments are osseous, dental, or non-skeletal in nature. The purpose of this review is to provide a detailed background of chemical analysis techniques focusing on elemental compositions that have been assessed for use in differentiating osseous, dental, and non-skeletal materials. More recently, chemical analysis studies have also focused on using the elemental composition of osseous/dental materials to evaluate species and provide individual discrimination, but have generally been successful only in small, closed groups, limiting their use forensically. Despite significant advances incorporating a variety of instruments, including handheld devices, further research is necessary to address issues in standardization, error rates, and sample size/diversity. Copyright © 2014 Forensic Science Society. Published by Elsevier Ireland Ltd. All rights reserved.

Proceedings of transuranium elements

International Nuclear Information System (INIS)

Anon.

1992-01-01

The identification of the first synthetic elements was established by chemical evidence. Conclusive proof of the synthesis of the first artificial element, technetium, was published in 1937 by Perrier and Segre. An essential aspect of their achievement was the prediction of the chemical properties of element 43, which had been missing from the periodic table and which was expected to have properties similar to those of manganese and rhenium. The discovery of other artificial elements, astatine and francium, was facilitated in 1939-1940 by the prediction of their chemical properties. A little more than 50 years ago, in the spring of 1940, Edwin McMillan and Philip Abelson synthesized element 93, neptunium, and confirmed its uniqueness by chemical means. On August 30, 1940, Glenn Seaborg, Arthur Wahl, and the late Joseph Kennedy began their neutron irradiations of uranium nitrate hexahydrate. A few months later they synthesized element 94, later named plutonium, by observing the alpha particles emitted from uranium oxide targets that had been bombarded with deuterons. Shortly thereafter they proved that is was the second transuranium element by establishing its unique oxidation-reduction behavior. The symposium honored the scientists and engineers whose vision and dedication led to the discovery of the transuranium elements and to the understanding of the influence of 5f electrons on their electronic structure and bonding. This volume represents a record of papers presented at the symposium

A study of essential elements in ancient Thai fighting swords by chemical and nuclear techniques

International Nuclear Information System (INIS)

Janposri, K.

1980-01-01

Four ancient Thai fighting swords from the Bangkok National Museum and iron ore from Kao Tab Kwai, Lopburi were studied by neutron activation analysis, metallography and chemical analysis. The results of these scientific studies show that all of these four swords are made of plain carbon steel, containing trace elements which have no effect on the physical and mechanical properties of the steel. The trace elements which were found in the iron ore are quite similar to those found in one of these swords. This means that the iron in one of the swords may have come from ore found at Kao Tab Kwai, Lopburi

Nomenclatural studies toward a world list of Diptera genus-group names. Part V

DEFF Research Database (Denmark)

Evenhuis, Neal L.; Pape, Thomas; Pont, Adrian C.

and method of fixation, current status of the name, family placement, and a list of any emendations of it that have been found in the literature. Remarks are given to clarify nomenclatural or taxonomic information. In addition, an index to all the species-group names of Diptera proposed by Macquart (3...

Determination of chemical elements in Eucalyptus grandis, manured with Ballad's, by neutrons activation analysis

International Nuclear Information System (INIS)

Mateus, Natalina de Fatima; Madi Filho, Tufic

2007-01-01

The biosolid is a mud resulting from the biological treatment of wasted liquids. It is considered as a profitable alternative and important to minimize the environmental impact generated by the sewage thrown in to sanitary lands, in forest cultures like the Eucalyptus grandis. The objective of this work was to detect which chemical elements are present in Eucalyptus grandis samples, fertilized with different quantities of biosolid. The eucalyptuses of Estacao Experimental de Ciencias Florestais of Itatinga were planted in March of 1998 and collected with five years old. The used biosolid was produced by Station of Treatment of Sewer of Barueri - SP, classified as kind B. For the determination of the presence and quantity of chemical elements in the eucalyptus samples, an analysis technique by neutronic activation (NAA) was used followed by gamma rays spectroscopy. The samples were irradiated in the Nuclear Reactor IEA-R1 of IPEN-SP, followed by the measure of induced gamma rays activity, using a Detector HPGe. The presence, mainly of Br, Mn, Na and K, was detected in all analyzed samples. (author)

Versatile protein recognition by the encoded display of multiple chemical elements on a constant macrocyclic scaffold

Science.gov (United States)

Li, Yizhou; De Luca, Roberto; Cazzamalli, Samuele; Pretto, Francesca; Bajic, Davor; Scheuermann, Jörg; Neri, Dario

2018-03-01

In nature, specific antibodies can be generated as a result of an adaptive selection and expansion of lymphocytes with suitable protein binding properties. We attempted to mimic antibody-antigen recognition by displaying multiple chemical diversity elements on a defined macrocyclic scaffold. Encoding of the displayed combinations was achieved using distinctive DNA tags, resulting in a library size of 35,393,112. Specific binders could be isolated against a variety of proteins, including carbonic anhydrase IX, horseradish peroxidase, tankyrase 1, human serum albumin, alpha-1 acid glycoprotein, calmodulin, prostate-specific antigen and tumour necrosis factor. Similar to antibodies, the encoded display of multiple chemical elements on a constant scaffold enabled practical applications, such as fluorescence microscopy procedures or the selective in vivo delivery of payloads to tumours. Furthermore, the versatile structure of the scaffold facilitated the generation of protein-specific chemical probes, as illustrated by photo-crosslinking.

Solution of the diffusion equations for several groups by the finite elements method

International Nuclear Information System (INIS)

Arredondo S, C.

1975-01-01

The code DELFIN has been implemented for the solution of the neutrons diffusion equations in two dimensions obtained by applying the approximation of several groups of energy. The code works with any number of groups and regions, and can be applied to thermal reactors as well as fast reactor. Providing it with the diffusion coefficients, the effective sections and the fission spectrum we obtain the results for the systems multiplying constant and the flows of each groups. The code was established using the method of finite elements, which is a form of resolution of the variational formulation of the equations applying the Ritz-Galerkin method with continuous polynomial functions by parts, in one case of the Lagrange type with rectangular geometry and up to the third grade. The obtained results and the comparison with the results in the literature, permit to reach the conclusion that it is convenient, to use the rectangular elements in all the cases where the geometry permits it, and demonstrate also that the finite elements method is better than the finite differences method. (author)

Advanced chemical analysis service for elements, radionuclides and phases

International Nuclear Information System (INIS)

Sansoni, B.

1986-01-01

A review is given on the structure, organisation and performance of the chemical analysis service of the Central Department for Chemical Analysis at the Kernforschungsanlage Juelich GmbH. The research and development programs together with the infrastructure of the Centre afford to analyse almost all stable elements of the periodical table in almost any material. The corresponding chemical analysis service has been organized according to a new modular system of analytical steps. According to this, the most complicated and, therefore, most general case of an analytical scheme for element and radionuclide analysis in any type of material can be differentiated into about 14 different steps, the modules. They are more or less independent of the special problem. The laboratory is designed and organized according to these steps. (orig./PW) [de

Behavior of radon, chemical compounds and stable elements in underground water

International Nuclear Information System (INIS)

Lopez R, N.; Segovia, N.; Lopez, M.B.E.; Pena, P.; Armienta, M.A.; Godinez, L.; Seidel, J.L.

2001-01-01

The radon behavior, chemical compounds, major and trace elements in water samples of four springs and three wells of urban and agricultural zones around the Jocotitlan volcano and El Oro region was determined, both of them located in the medium part of the Mexican neo-volcanic axis. The 222 Rn was measured by the liquid scintillation method, the analysis of major components was realized with conventional chemical techniques, while the trace elements were quantified using an Icp-Ms. The average values of the radon concentrations obtained during one year were constant relatively, in an interval from 0.97 to 4.99 Bq/lt indicating a fast transport from the reload area toward the sampling points. the compounds, major and trace elements showed differences which indicate distinct origins of water from the site studies. (Author)

Provenance determination of pottery by trace element analysis. Problems, solutions and applications

International Nuclear Information System (INIS)

Mommsen, H.

2001-01-01

Provenance determinations of pottery by chemical analysis is reviewed and shown to work well. Since pottery is produced from a well homogenized clay paste according to a certain recipe, sharp elemental patterns are expected for a series of products having the same origin. To obtain such patterns when forming compositional groups of pottery, a consideration of experimental errors, a correction for dilution and a choice of only stable elements is necessary. The patterns thus obtained will have low probability of overlap with groups of different origin. Examples for well defined groups of German stonewares and of Mycenaean wares from the Peloponnese are recorded. (author)

A Chemical Eight Group Separation Method for Routine Use in Gamma Spectrometric Analysis

Energy Technology Data Exchange (ETDEWEB)

Samsahl, K

1961-04-15

A method for the separation of chemical elements in 8 groups suitable for gamma spectrometric analysis has been developed. One group of elements is separated by distillation during dissolution of the sample. The other groups are obtained by means of short ion exchange columns coupled in series An anion exchange column saturated with chloride ions separates chloride complexes, peroxides and other anions from a 3-n HCl + 0.3 % H{sub 2}O{sub 2} sample solution. Some of the chloride complexes are eluted with 0.1-n HCl + 0.3 % H{sub 2}O{sub 2} and subsequently adsorbed as cations on a cation exchange column in hydrogen form. A few eluted elements which do not form cations in this case are found in the effluent. Elements passing the anion exchange column in chloride form without adsorption are separated from a H{sub 2}O solution as citrate complexes, hydroxides, cations and hexametaphosphate complexes. This is done by coupling in series two anion exchange columns subsequently in citrate and hydroxide form and followed by a cation exchanger in sodium form. A mixed bed column ends the series. The behaviour in the separation series of most elements forming gamma emitting isotopes with half lives exceeding 10 minutes on irradiation with thermal neutrons has been studied. The method has been used, routinely for one year.

Cytogenetic mapping of the Muller F element genes in Drosophila willistoni group.

Science.gov (United States)

Pita, Sebastián; Panzera, Yanina; Lúcia da Silva Valente, Vera; de Melo, Zilpa das Graças Silva; Garcia, Carolina; Garcia, Ana Cristina Lauer; Montes, Martín Alejandro; Rohde, Claudia

2014-10-01

Comparative genomics in Drosophila began in 1940, when Muller stated that the ancestral haploid karyotype of this genus is constituted by five acrocentric chromosomes and one dot chromosome, named A to F elements. In some species of the willistoni group such as Drosophila willistoni and D. insularis, the F element, instead of a dot chromosome, has been incorporated into the E element, forming chromosome III (E + F fusion). The aim of this study was to investigate the scope of the E + F fusion in the willistoni group, evaluating six other species. Fluorescent in situ hybridization was used to locate two genes of the F element previously studied-cubitus interruptus (ci) and eyeless (ey)-in species of the willistoni and bocainensis subgroups. Moreover, polytene chromosome photomaps corresponding to the F element (basal portion of chromosome III) were constructed for each species studied. In D. willistoni, D. paulistorum and D. equinoxialis, the ci gene was located in subSectction 78B and the ey gene in 78C. In D. tropicalis, ci was located in subSection 76B and ey in 76C. In species of the bocainensis subgroup, ci and ey were localized, respectively, at subsections 76B and 76C in D. nebulosa and D. capricorni, and 76A and 76C in D. fumipennis. Despite the differences in the subsection numbers, all species showed the same position for ci and ey. The results confirm the synteny of E + F fusion in willistoni and bocainensis subgroups, and allow estimating the occurrence of this event at 15 Mya, at least.

Chemical elements in invertebrate orders for environmental quality studies

Energy Technology Data Exchange (ETDEWEB)

Magalhaes, Marcelo R.L.; Franca, Elvis J.; Paiva, Jose D.S.; Hazin, Clovis A., E-mail: marcelo_rlm@hotmail.com, E-mail: ejfranca@cnen.gov.br, E-mail: dan-paiva@hotmail.com, E-mail: chazin@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Fonseca, Felipe Y.; Fernandes, Elisabete A. de Nadai; Bacchi, Marcio A., E-mail: felipe-yamada@hotmail.com, E-mail: lis@cena.usp.br, E-mail: mabacchi@cena.usp.br [Centro de Energia Nuclear na Agricultura (CENA/USP), Piracicaba, SP (Brazil)

2013-07-01

Among the biomonitors of environmental quality, there is a lack of studies on using invertebrates to evaluate quantitatively chemical elements in ecosystems. This group of animals is quite numerous, widely distributed and adaptable to the most diverse environmental conditions. These features are very useful for the environmental quality assessment, as well as the several occurring insect-plant interactions performing essential functions in ecosystems. The objective of this work is to study the variability of chemical composition of invertebrate orders for using in environmental quality monitoring studies. Instrumental neutron activation analysis - INAA was applied to determine some nutrients and trace elements in invertebrate samples. Sampling by pitfall traps was carried out in riverine ecosystems from the urban area from the Piracicaba Municipality, State of Sao Paulo, Brazil. Invertebrate and reference material samples were irradiated in the nuclear research reactor IEA-R1, Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN. Fragments of a Ni-Cr alloy were irradiated for monitoring the thermal neutron flux. Hymenoptera order was considered the most representative according to the total number of sampled species (about 60%). Significant amounts of Ba, Br, Fe and Sc were found in invertebrates of the order Opiliones. Potassium, rubidium and zinc were highly accumulated in species from Blattodea order, indicating a consistent pattern of accumulation for this invertebrate order. Taking into account the abundance of Hymenoptera order, the chemical composition of its species was significant different at the 95% confidence level for Br and Na in the sampled locals. (author)

Chemical elements in invertebrate orders for environmental quality studies

International Nuclear Information System (INIS)

Magalhaes, Marcelo R.L.; Franca, Elvis J.; Paiva, Jose D.S.; Hazin, Clovis A.; Fonseca, Felipe Y.; Fernandes, Elisabete A. de Nadai; Bacchi, Marcio A.

2013-01-01

Among the biomonitors of environmental quality, there is a lack of studies on using invertebrates to evaluate quantitatively chemical elements in ecosystems. This group of animals is quite numerous, widely distributed and adaptable to the most diverse environmental conditions. These features are very useful for the environmental quality assessment, as well as the several occurring insect-plant interactions performing essential functions in ecosystems. The objective of this work is to study the variability of chemical composition of invertebrate orders for using in environmental quality monitoring studies. Instrumental neutron activation analysis - INAA was applied to determine some nutrients and trace elements in invertebrate samples. Sampling by pitfall traps was carried out in riverine ecosystems from the urban area from the Piracicaba Municipality, State of Sao Paulo, Brazil. Invertebrate and reference material samples were irradiated in the nuclear research reactor IEA-R1, Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN. Fragments of a Ni-Cr alloy were irradiated for monitoring the thermal neutron flux. Hymenoptera order was considered the most representative according to the total number of sampled species (about 60%). Significant amounts of Ba, Br, Fe and Sc were found in invertebrates of the order Opiliones. Potassium, rubidium and zinc were highly accumulated in species from Blattodea order, indicating a consistent pattern of accumulation for this invertebrate order. Taking into account the abundance of Hymenoptera order, the chemical composition of its species was significant different at the 95% confidence level for Br and Na in the sampled locals. (author)

Platinum-group elements fractionation by selective complexing, the Os, Ir, Ru, Rh-arsenide-sulfide systems above 1020 °C

Science.gov (United States)

Helmy, Hassan M.; Bragagni, Alessandro

2017-11-01

The platinum-group element (PGE) contents in magmatic ores and rocks are normally in the low μg/g (even in the ng/g) level, yet they form discrete platinum-group mineral (PGM) phases. IPGE (Os, Ir, Ru) + Rh form alloys, sulfides, and sulfarsenides while Pt and Pd form arsenides, tellurides, bismuthoids and antimonides. We experimentally investigate the behavior of Os, Ru, Ir and Rh in As-bearing sulfide system between 1300 and 1020 °C and show that the prominent mineralogical difference between IPGE (+Rh) and Pt and Pd reflects different chemical preference in the sulfide melt. At temperatures above 1200 °C, Os shows a tendency to form alloys. Ruthenium forms a sulfide (laurite RuS2) while Ir and Rh form sulfarsenides (irarsite IrAsS and hollingworthite RhAsS, respectively). The chemical preference of PGE is selective: IPGE + Rh form metal-metal, metal-S and metal-AsS complexes while Pt and Pd form semimetal complexes. Selective complexing followed by mechanical separation of IPGE (and Rh)-ligand from Pt- and Pd-ligand associations lead to PGE fractionation.

GLOBAL AND REGIONAL GEOCHEMICAL INDEXES OF PRODUCTION OF CHEMICAL ELEMENTS

Directory of Open Access Journals (Sweden)

Nikolay S. Kasimov

2014-01-01

Full Text Available This paper presents a geochemical assessment of the primary involvement of chemical elements in technogenesis in the world and individual countries. In order to compare the intensity of production of various chemical elements in different countries, the authors have introduced a number of new terms and parameters. The new term is “abstract rock” (AR - an elemental equivalent, whose average composition corresponds to the average chemical composition of the upper continental crust. The new parameters are: “conditional technophility of an element” (TY, “specific technophility” (TYN “regional conditional technophility” (TYR, “specific regional technophility” (TN, and “density of regional conditional technophility” (TS. TY equals to the tons of AR per year necessary for the production of the current level of the element. TY of different elements has been estimated for 2008-2010. The highest TY values are associated with C, S, N, Ra, and Au. TY of many micro- and ultramicroelements is of the order of n•1011t. TYN reflects the volume of AR per the world’s capita. TYN changes from the 1960s to 2010 indicates that the Earth’s population is growing much faster than its demand for many chemical elements. TYR, TN, and TS were used for the integrated assessment of technogenesis at the regional scale; they reflect the intensity of the technogenesis process at the level of individual countries and allow comparing countries with different levels of elements production, population, and areas. The TN and TS levels of the leaders in extraction of natural resources are below these values in other countries due to the large territories (Russia, USA, Canada, Australia, Saudi Arabia, Kazakhstan, Argentina, Bolivia, Venezuela, Colombia, Zambia, Mali, Libya, Mongolia, and Sudan, to the large population (Indonesia, Vietnam, the Philippines, Bangladesh, Nigeria, or to both high spatial and demographic dimensions (India, Brazil, France, Egypt

Prompt gamma-ray spectroscopy and its use for the elemental chemical analysis

International Nuclear Information System (INIS)

Deconninck, G.; Demortier, G.; Bodart, F.

The elemental chemical analysis by nuclear techniques has been widely developed since a quarter of century. In this review the analysis by irradiation of the the sample (solid or liquid) of a majority of chemical elements by means of the charged particles and the detection during this irradiation of the gamma photons characteristic of the element are considered. After a brief account of the physical phenomena peculiar to the prompt detection of photons in comparison with the activation methods where a delayed activity is measured, a brief description of the experimental equipment for this kind of analysis is given. A comprehensive critical survey of the recent applications to the analysis of metals, semiconductors and electric insulating substances is presented. The necessary informations for the choice of the nuclear reaction to use for a specific analysis are contained in a set of tables. (AF)

Influence of relativistic effect on chemical properties of element 104; Wplyw efektu relatywistycznego na wlasnosci chemiczne pierwiastka 104

Energy Technology Data Exchange (ETDEWEB)

Bilewicz, A.

1997-12-31

The influence of relativistic effect upon chemical properties of element 104 is discussed. An original method of measurements of adsorption on the surface of thin film of cobalt ferrocyanate was developed and applied for the studies of 104{sup 4+} hydrolysis. Results of this experiments indicate that in the Group 4 tendency to hydrolysis decreases in the order 104{sup 4+}>Zr{sup 4+}>Hf{sup 4+}. The results were explained on the basis of relativistic effect. Unexpected chemical properties of element 104 in aqueous solutions indicate, that due to relativistic effect element 104 differs distinctly from its congeners - Zr and Hf. In contrary it becomes similar to the lightest element in the Group, Ti, through atomic mass of latter is 213 unit less. (author). 119 refs, 22 figs, 7 tabs.

Anthroponyms in Finno-Permic Compound Plant Names

Directory of Open Access Journals (Sweden)

Igor V. Brodsky

2017-07-01

Full Text Available With reference to Finno-Permic languages (a branch of Finno-Ugric languages excluding Ugric languages, the article analyses compound names of plants (phytonyms containing Permic languages, which, inter alia, can be explained by the incompleteness of collected data. Most of phytonyms with anthroponymic elements are attested in the Finnish and Estonian languages, while in the other Finno-Permic languages such attestations are rare. The anthroponyms appearing in names of plants are divided into two groups: a personal names of Biblical origin (e.g. Finnish Aapraham, Aatam, Jeesus, Maaria, b other anthroponyms. In the first group, the most numerous are Balto-Fennic phytonyms with the names Johannes and Maria and their national variants. The name Johannes (Finnish Juhannus, Estonian Jaan is most often present in the names of herbaceous plants flourishing in the period of celebration of Saint John’s Eve. Traditionally, this feast is associated with numerous rites and customs in which some plants play a significant role. An interesting formal feature of Balto-Fennic deanthroponymic compound names of plants is alliteration, i.e. repetition of identical or similar sound clusters in the beginning of each part of the word, as in Finnish liisanlilukka ‘stone bramble,’ simonsien’ ‘chanterelle, girolle’.

Oxidative Addition and Reductive Elimination at Main-Group Element Centers.

Science.gov (United States)

Chu, Terry; Nikonov, Georgii I

2018-04-11

Oxidative addition and reductive elimination are key steps in a wide variety of catalytic reactions mediated by transition-metal complexes. Historically, this reactivity has been considered to be the exclusive domain of d-block elements. However, this paradigm has changed in recent years with the demonstration of transition-metal-like reactivity by main-group compounds. This Review highlights the substantial progress achieved in the past decade for the activation of robust single bonds by main-group compounds and the more recently realized activation of multiple bonds by these elements. We also discuss the significant discovery of reversible activation of single bonds and distinct examples of reductive elimination at main-group element centers. The review consists of three major parts, starting with oxidative addition of single bonds, proceeding to cleavage of multiple bonds, and culminated by the discussion of reversible bond activation and reductive elimination. Within each subsection, the discussion is arranged according to the type of bond being cleaved or formed and considers elements from the left to the right of each period and down each group of the periodic table. The majority of results discussed in this Review come from the past decade; however, earlier reports are also included to ensure completeness.

Determination of Elements in Normal and Leukemic Human Whole Blood by Neutron Activation Analysis

Energy Technology Data Exchange (ETDEWEB)

Brune, D; Frykberg, B; Samsahl, K; Wester, P O

1961-11-15

By means of gamma-spectrometry the following elements were simultaneously determined in normal and leukemic human whole blood: Cu, Mn, Zn, Sr, Na, P, Ca, Rb, Cd, Sb, Au, Cs and Fe. Chemical separations were performed according to a group separation method using ion-exchange technique. No significant difference between the concentrations of the elements in normal- and leukemic blood was observed.

Determination of Elements in Normal and Leukemic Human Whole Blood by Neutron Activation Analysis

International Nuclear Information System (INIS)

Brune, D.; Frykberg, B.; Samsahl, K.; Wester, P.O.

1961-11-01

By means of gamma-spectrometry the following elements were simultaneously determined in normal and leukemic human whole blood: Cu, Mn, Zn, Sr, Na, P, Ca, Rb, Cd, Sb, Au, Cs and Fe. Chemical separations were performed according to a group separation method using ion-exchange technique. No significant difference between the concentrations of the elements in normal- and leukemic blood was observed

Elemental Food for Thought

Science.gov (United States)

Cady, Susan

2005-01-01

One of the first tasks students learn in chemistry is to pronounce and spell the names of elements and learn their corresponding chemical symbols. Repetitive oral recitation is commonly used to learn this information, but games and puzzles can make this task creative, variable, and fun. Elemental Food for Thought is a puzzlelike activity that…

[Distribution of chemical elements in whole blood and plasma].

Science.gov (United States)

Barashkov, G K; Zaĭtseva, L I; Kondakhchan, M A; Konstantinova, E A

2003-01-01

The distribution factor (Fd) of 35 elements of plasma and whole blood in 26 healthy men and women was detected by ICP-OES. Usilig this parameter the elements were subdivided in 3 pools. 9 of them have Fd higher than 1.5 ("elements of plasma"-Ag, Ca, Cu, In, Li, Na, Se, Si, Sr); 6 have lower than 0.5 ("elements of blood cells"-Fe, K, Mn, Ni, V, Zn), other 20-about 1 ("blood elements"). Fd of all elements depends on ionic radius. Elements of 2nd sub-groups of all groups of Mendeleev's periodic table ("heavy metals") depend on the similar law: "with growing of ionic radius the concentration of elements in plasma enhances". In alkaline metals Fd depends on the opposite law:" with growing of ionic radius of alkaline metal the quantity of elements in blood cells enhance". Dependence of Fd on the value of atomic mass in periods or in exterior electronic cloud (s-, p-, d-, f-) was not established. The table of distribution of all detected elements in whole blood in relation to 8 macroelements (Ca, Mg, K, Na, S, P, Fe, Zn,) is presented, as a basic diagnostic criteria in metal-ligand homeostasis disturbance.

Chemistry of the transactinide elements

International Nuclear Information System (INIS)

Schaedel, M.

1995-01-01

The experimentally known chemical properties of the transactinide elements 104 and 105, and the experimental techniques used to study these properties on an atom-at-a-time base, are reviewed. The production of transactinides in heavy ion reactions and the specific aspects of chemical separations with single atoms is briefly discussed. The chemical properties of the first two transactinide elements are compared with the lighter element homologs in group 4 and 5 of the Periodic Table and with the expected behaviour obtained from most recent atomic and molecular calculations which take the increasingly strong relativistic effect into account. Elements 104 and 105 behave as transactinide elements and, in general, exhibit properties characteristic of their position in group 4 and 5 of the Periodic Table. However, surprising deviations of the chemical properties from expectations based on simple extrapolations have been observed. It is shown that the chemical properties of the heaviest elements cannot reliably be predicted by simple extrapolations. Prospects to extend our chemical knowledge at the top end of the Periodic Table are discussed. (orig.)

Evaluation of group electronegativities and hardness (softness) of group 14 elements and containing functional groups through density functional theory and correlation with NMR spectra data

International Nuclear Information System (INIS)

Vivas-Reyes, R.; Aria, A.

2008-01-01

Quantum Chemical calculations for group 14 elements of Periodic Table (C, Si, Ge, Sn, Pb) and their functional groups have been carried out using Density Functional Theory (DFT) based reactivity descriptors such as group electronegativities, hardness and softness. DFT calculations were performed for a large series of tetra coordinated Sn compounds of the CH 3 SnRR'X type, where X is a halogen and R and R' are alkyl, halogenated alkyl, alkoxy, or alkyl thio groups. The results were interpreted in terms of calculated electronegativity and hardness of the SnRR'X groups, applying a methodology previously developed by Geerlings and coworkers (J. Phys. Chem. 1993, 97, 1826). These calculations allowed to see the regularities concerning the influence of the nature of organic groups RR' and inorganic group X on electronegativities and hardness of the SnRR'X groups; in this case, it was found a very good correlation between the electronegativity of the fragment and experimental 119 Sn chemical shifts, a property that sensitively reflects the change in the valence electronic structure of molecules. This work was complemented with the study of some compounds of the EX and ER types, where E= C, Si, Ge, Sn and R= CH 3 , H, which was performed to study the influence that the central atom has on the electronegativity and hardness of molecules, or whether these properties are mainly affected for the type of ligand bound to the central atom. All these calculations were performed using the B3PW91 functional together with the 6-3 1 1 + + G basis set level for H, C, Si, Ge, F, Cl and Br atoms and the 3-21G for Sn and I atoms. (author)

Evaluation of group electronegativities and hardness (softness) of group 14 elements and containing functional groups through density functional theory and correlation with NMR spectra data

Energy Technology Data Exchange (ETDEWEB)

Vivas-Reyes, R.; Aria, A. [Universidad de Cartagena, Cartagena (Colombia). Facultad de Ciencias Naturales y Exactas. Grupo de Quimica Cuantica y Computacional]. E-mail: rvivasr@unicartagena.edu.co

2008-07-01

Quantum Chemical calculations for group 14 elements of Periodic Table (C, Si, Ge, Sn, Pb) and their functional groups have been carried out using Density Functional Theory (DFT) based reactivity descriptors such as group electronegativities, hardness and softness. DFT calculations were performed for a large series of tetra coordinated Sn compounds of the CH{sub 3}SnRR'X type, where X is a halogen and R and R' are alkyl, halogenated alkyl, alkoxy, or alkyl thio groups. The results were interpreted in terms of calculated electronegativity and hardness of the SnRR'X groups, applying a methodology previously developed by Geerlings and coworkers (J. Phys. Chem. 1993, 97, 1826). These calculations allowed to see the regularities concerning the influence of the nature of organic groups RR' and inorganic group X on electronegativities and hardness of the SnRR'X groups; in this case, it was found a very good correlation between the electronegativity of the fragment and experimental {sup 119}Sn chemical shifts, a property that sensitively reflects the change in the valence electronic structure of molecules. This work was complemented with the study of some compounds of the EX and ER types, where E= C, Si, Ge, Sn and R= CH{sub 3}, H, which was performed to study the influence that the central atom has on the electronegativity and hardness of molecules, or whether these properties are mainly affected for the type of ligand bound to the central atom. All these calculations were performed using the B3PW91 functional together with the 6-3 1 1 + + G basis set level for H, C, Si, Ge, F, Cl and Br atoms and the 3-21G for Sn and I atoms. (author)

Redox reactions for group 5 elements, including element 105, in aqueous solutions

International Nuclear Information System (INIS)

Ionova, G.V.; Pershina, V.; Johnson, E.; Fricke, B.; Schaedel, M.

1992-08-01

Standard redox potentials Edeg(M z+x /M z+ ) in acidic solutions for group 5 elements including element 105 (Ha) and the actinide, Pa, have been estimated on the basis of the ionization potentials calculated via the multiconfiguration Dirac-Fock method. Stability of the pentavalent state was shown to increase along the group from V to Ha, while that of the tetra- and trivalent states decreases in this direction. Our estimates have shown no extra stability of the trivalent state of hahnium. Element 105 should form mixed-valence complexes by analogy with Nb due to the similar values of their potentials Edeg(M 3+ /M 2+ ). The stability of the maximum oxidation state of the elements decreases in the direction 103 > 104 > 105. (orig.)

LLNL Chemical Kinetics Modeling Group

Energy Technology Data Exchange (ETDEWEB)

Pitz, W J; Westbrook, C K; Mehl, M; Herbinet, O; Curran, H J; Silke, E J

2008-09-24

The LLNL chemical kinetics modeling group has been responsible for much progress in the development of chemical kinetic models for practical fuels. The group began its work in the early 1970s, developing chemical kinetic models for methane, ethane, ethanol and halogenated inhibitors. Most recently, it has been developing chemical kinetic models for large n-alkanes, cycloalkanes, hexenes, and large methyl esters. These component models are needed to represent gasoline, diesel, jet, and oil-sand-derived fuels.

Survey of chemical speciation of trace elements using synchrotron radiation

International Nuclear Information System (INIS)

Gordon, B.M.

1985-01-01

Information concerning the chemical state of trace elements in biological systems generally has not been available. Such information for toxic elements and metals in metalloproteins could prove extremely valuable in the elucidation of their metabolism and other biological processes. The shielding of core electrons by binding electrons affect the energy required for creating inner-shell holes. Furthermore, the molecular binding and the symmetry of the local environment of an atom affect the absorption spectrum in the neighborhood of the absorption edge. X-ray absorption near-edge structure (XANES) using synchrotron radiation excitation can be used to provide chemical speciation information for trace elements at concentrations as low as 10 ppM. The structure and position of the absorption curve in the region of an edge can yield vital data about the local structure and oxidation state of the trace element in question. Data are most easily interpreted by comparing the observed edge structure and position with those of model compounds of the element covering the entire range of possible oxidation states. Examples of such analyses are reviewed. 14 refs., 1 fig

Genetic interpretations of elemental and chemical differences in a soil chronosequence, California

Science.gov (United States)

Harden, J.W.

1988-01-01

Soils developed on fluvial terraces in central California have similar parent materials, climatic settings, vegetation cover and slopes but range in age from 40,000 to 3,000,000 years. The soils have chemical compositions that change systematically with increasing age. Such chemical differentiation is most likely the result of long-term weathering and mineralogical transformations that occurred since deposition of terrace fills and stabilization of the geomorphic surfaces. The changes in composition with time closely mimic other studies on mineral weathering, in which alkali and alkali-earth elements are lost more rapidly than transitional elements. The relative rates of element loss were determined by changes in element ratios over time. Net losses and gains of elements in different size fractions were monitored by their concentrations relative to Zr, the most stable constituent. Both sand and finer size fractions have lost considerable amounts of Ca, Mg, Na and K. Aluminum appears to have been lost from the sand fraction and gained in the fine fraction over a 3-million-year-time-span. Although there is no evidence for losses of Fe and Ti from sands, there is a net influx of Fe and Ti into finer fractions, probably gained from undetectable yet significant weathering of sand grains. Etching of sand grains, clay mineralogy, and microprobe analyses also indicate that the soils have undergone these chemical transformations during their formation. Mineralogical analyses also mimic other studies on mineral weathering, in which the pyroxenes weather more rapidly than hornblende, which weathers more rapidly than sphene or zircon. ?? 1988.

Zinc and group V element co-implantation in indium phosphide

International Nuclear Information System (INIS)

Yu, Kin Man; Ridgway, M.C.

2000-01-01

Group V elements with mass ranging from 35 to 122 amu have been co-implanted with Zn in InP substrates. Co-implantation with all group V elements drastically reduced Zn out-diffusion and to a certain extent also inhibited Zn in-diffusion. The reduction in out-diffusion was insensitive to the group V element mass and thus, to implantation-induced damage. We believe the group V element excess created an In-vacancy excess that enhanced Zn substitution into the In sublattice. A maximum hole concentration of 7x10 18 cm -3 was achieved with P co-implantation. Electrochemical capacitance-voltage profiling clearly showed a decrease in hole concentration as a function of increasing group V element mass. This was attributed to differences in compensating residual implantation-induced damage

Contents of chemical elements in tissues of European badger (Meles meles affected by ovarian tumour – a case report

Directory of Open Access Journals (Sweden)

Karel Bukovjan

2014-01-01

Full Text Available Higher concentrations of chemical elements in animal tissues may be associated with tumours and may explain cancerogenity. In this study, selected chemical elements were measured in the liver, kidneys, muscles and tissues affected by tumour in a dead female European badger (Meles meles with a metastatic ovarian carcinoma. Atomic absorption spectroscopy was used for the assessment of concentrations of arsenic, cadmium, chromium, copper, lead, and zinc. AMA 254 analyser was used for the assessment of mercury concentration. Concentrations of heavy metals such as As, Cr, Cu, Zn, Cd, Pb, and total Hg amounted to 0.031, 0.16, 7.74, 44.54, 0.67, 0.67, and 0.36 mg·kg-1 in the tumour tissue. This is the first detection of ovarian tumour in a European badger (Meles meles which was systematically examined for the presence of chemical elements.

Encoding of Fundamental Chemical Entities of Organic Reactivity Interest using chemical ontology and XML.

Science.gov (United States)

Durairaj, Vijayasarathi; Punnaivanam, Sankar

2015-09-01

Fundamental chemical entities are identified in the context of organic reactivity and classified as appropriate concept classes namely ElectronEntity, AtomEntity, AtomGroupEntity, FunctionalGroupEntity and MolecularEntity. The entity classes and their subclasses are organized into a chemical ontology named "ChemEnt" for the purpose of assertion, restriction and modification of properties through entity relations. Individual instances of entity classes are defined and encoded as a library of chemical entities in XML. The instances of entity classes are distinguished with a unique notation and identification values in order to map them with the ontology definitions. A model GUI named Entity Table is created to view graphical representations of all the entity instances. The detection of chemical entities in chemical structures is achieved through suitable algorithms. The possibility of asserting properties to the entities at different levels and the mechanism of property flow within the hierarchical entity levels is outlined. Copyright © 2015 Elsevier Inc. All rights reserved.

Reconstruction of centennial-scale fluxes of chemical elements in the Australian coastal environment using seagrass archives

KAUST Repository

Serrano, Oscar; Davis, Grace; Lavery, Paul S.; Duarte, Carlos M.; Martinez-Cortizas, Antonio; Mateo, Miguel Angel; Masqué , Pere; Arias-Ortiz, Ariane; Rozaimi, Mohammad; Kendrick, Gary A.

2015-01-01

The study of a Posidonia australis sedimentary archive has provided a record of changes in element concentrations (Al, Fe, Mn, Pb, Zn, Cr, Cd, Co, As, Cu, Ni and S) over the last 3000 years in the Australian marine environment. Human-derived contamination in Oyster Harbor (SW Australia) started ~. 100 years ago (AD ~. 1900) and exponentially increased until present. This appears to be related to European colonization of Australia and the subsequent impact of human activities, namely mining, coal and metal production, and extensive agriculture. Two contamination periods of different magnitude have been identified: Expansion period (EXP, AD ~. 1900-1970) and Establishment period (EST, AD ~. 1970 to present). Enrichments of chemical elements with respect to baseline concentrations (in samples older than ~. 115 cal. years BP) were found for all elements studied in both periods, except for Ni, As and S. The highest enrichment factors were obtained for the EST period (ranging from 1.3-fold increase in Cu to 7.2-fold in Zn concentrations) compared to the EXP period (1.1-fold increase for Cu and Cr to 2.4-fold increase for Pb). Zinc, Pb, Mn and Co concentrations during both periods were 2- to 7-fold higher than baseline levels. This study demonstrates the value of Posidonia mats as long-term archives of element concentrations and trends in coastal ecosystems. We also provide preliminary evidence on the potential for Posidonia meadows to act as significant long-term biogeochemical sinks of chemical elements.

Reconstruction of centennial-scale fluxes of chemical elements in the Australian coastal environment using seagrass archives

KAUST Repository

Serrano, Oscar

2015-10-02

The study of a Posidonia australis sedimentary archive has provided a record of changes in element concentrations (Al, Fe, Mn, Pb, Zn, Cr, Cd, Co, As, Cu, Ni and S) over the last 3000 years in the Australian marine environment. Human-derived contamination in Oyster Harbor (SW Australia) started ~. 100 years ago (AD ~. 1900) and exponentially increased until present. This appears to be related to European colonization of Australia and the subsequent impact of human activities, namely mining, coal and metal production, and extensive agriculture. Two contamination periods of different magnitude have been identified: Expansion period (EXP, AD ~. 1900-1970) and Establishment period (EST, AD ~. 1970 to present). Enrichments of chemical elements with respect to baseline concentrations (in samples older than ~. 115 cal. years BP) were found for all elements studied in both periods, except for Ni, As and S. The highest enrichment factors were obtained for the EST period (ranging from 1.3-fold increase in Cu to 7.2-fold in Zn concentrations) compared to the EXP period (1.1-fold increase for Cu and Cr to 2.4-fold increase for Pb). Zinc, Pb, Mn and Co concentrations during both periods were 2- to 7-fold higher than baseline levels. This study demonstrates the value of Posidonia mats as long-term archives of element concentrations and trends in coastal ecosystems. We also provide preliminary evidence on the potential for Posidonia meadows to act as significant long-term biogeochemical sinks of chemical elements.

Speciation of trace elements in biological samples by nuclear analytical and related techniques coupled with chemical and biochemical separation

International Nuclear Information System (INIS)

Chen, C.Y.; Gao, Y.X.; Li, B.; Yu, H.W.; Li, Y.F.; Sun, J.; Chai, Z.F.

2005-01-01

In the past, most analytical problems relating to biological systems were addressed by measuring the total concentrations of elements. Now there is increasing interest of the importance of their chemical forms, in which an element is present in biological systems, e.g., the oxidation state, the binding state with macromolecules, or even the molecular structure. The biological effects of chromium, which is classified as an essential nutrient, are dependent upon its oxidation. state. In general, trivalent chromium is biochemically active, whereas hexavalent chromium is considered to be toxic. Mercury is one of serious environmental persistent pollutants. However, organic forms of mercury are known to possess much higher toxicity than inorganic mercury. Therefore, information on speciation is critically required in order to better understanding of their bioavailability, metabolism, transformation, and toxicity in vivo. Recently, chemical speciation of selenium, mercury, copper, zinc, iron, and so on, has been investigated by INAA, ICP-MS, XRF, EXAFS and related techniques combined with chemical and biochemical separation (extraction, chromatography, gel electrophoresis, etc.). INAA, XRF, and ICP-MS have superior advantages in aspect of multielemental analysis with high accuracy and sensitivity, which render the possibility of analyzing various elements of interest simultaneously. These offline or online techniques have been flexibly applied to different biological matrixes, such as human hair, serum, urine, various tissues and organs in our researches. In addition, EXAFS provides structural information about the moiety of metal centers up to a distance of approximately 4-5 Anstrom. For instance, hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. Imbalance of elements, such as Se, Zn, Fe, Cu, Cd, Ca, etc., has been found in the whole blood or serum of patients with HCC. We found that the profiles of Se, Cd, Fe, Zn and Cu-containing proteins

Chemical Abundances of Hydrostatic and Explosive Alpha-elements in Sagittarius Stream Stars

Science.gov (United States)

Carlin, Jeffrey L.; Sheffield, Allyson A.; Cunha, Katia; Smith, Verne V.

2018-05-01

We analyze chemical abundances of stars in the Sagittarius (Sgr) tidal stream using high-resolution Gemini+GRACES spectra of 42 members of the highest surface-brightness portions of both the trailing and leading arms. Targets were chosen using a 2MASS+WISE color–color selection, combined with the Large Sky Area Multi-Object Fibre Spectroscopic Telescope (LAMOST) radial velocities. In this Letter, we analyze [Fe/H] and α-elements produced by both hydrostatic (O, Mg) and explosive (Si, Ca, Ti) nucleosynthetic processes. The average [Fe/H] for our Sgr stream stars is lower than that for stars in the Sgr core, and stars in the trailing and leading arms show systematic differences in [Fe/H]. Both hydrostatic and explosive elements are depleted relative to Milky Way (MW) disk and halo stars, with a larger gap between the MW trend and Sgr stars for the hydrostatic elements. Chemical abundances of Sgr stream stars show similar patterns to those measured in the core of the Sgr dSph. We explore the ratio of hydrostatic to explosive α-elements [α h/ex] (which we refer to as the “HEx ratio”). Our observed HEx ratio trends for Sgr debris are deficient relative to MW stars. Via simple chemical evolution modeling, we show that these HEx ratio patterns are consistent with a Sgr IMF that lacks the most massive stars. This study provides a link between the chemical properties in the intact Sgr core and the significant portion of the Sgr system’s luminosity that is estimated to currently reside in the streams.

Effects of chemical functional groups on elemental mercury adsorption on carbonaceous surfaces

Energy Technology Data Exchange (ETDEWEB)

Liu Jing, E-mail: liujing27@mail.hust.edu.cn [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan 430074 (China); Cheney, Marcos A. [Department of Natural Sciences, University of Maryland Eastern Shore, Princess Anne, MD 21853 (United States); Wu Fan; Li Meng [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan 430074 (China)

2011-02-15

A systematic theoretical study using density functional theory is performed to provide molecular-level understanding of the effects of chemical functional groups on mercury adsorption on carbonaceous surfaces. The zigzag and armchair edges were used in modeling the carbonaceous surfaces to simulate different adsorption sites. The edge atoms on the upper side of the models are unsaturated to simulate active sites. All calculations (optimizations, energies, and frequencies) were made at B3PW91 density functional theory level, using RCEP60VDZ basis set for mercury and 6-31G(d) pople basis set for other atoms. The results indicate that the embedding of halogen atom can increase the activity of its neighboring site which in turn increases the adsorption capacity of the carbonaceous surface for Hg{sup 0}. The adsorption belongs to chemisorptions, which is in good agreement with the experimental results. For the effects of oxygen functional groups, lactone, carbonyl and semiquinone favor Hg{sup 0} adsorption because they increase the neighboring site's activity for mercury adsorption. On the contrary, phenol and carboxyl functional groups show a physisorption of Hg{sup 0}, and reduce Hg capture. This result can explain the seemingly conflicting experimental results reported in the literature concerning the influence of oxygen functional groups on mercury adsorption on carbonaceous surface.

Flavour chemicals in a sample of non-cigarette tobacco products without explicit flavour names sold in New York City in 2015.

Science.gov (United States)

Farley, Shannon M; Schroth, Kevin Rj; Grimshaw, Victoria; Luo, Wentai; DeGagne, Julia L; Tierney, Peyton A; Kim, Kilsun; Pankow, James F

2018-03-01

Youth who experiment with tobacco often start with flavoured products. In New York City (NYC), local law restricts sales of all tobacco products with 'characterising flavours' except for 'tobacco, menthol, mint and wintergreen'. Enforcement is based on packaging: explicit use of a flavour name (eg, 'strawberry') or image depicting a flavour (eg, a fruit) is presumptive evidence that a product is flavoured and therefore prohibited. However, a tobacco product may contain significant levels of added flavour chemicals even when the label does not explicitly use a flavour name. Sixteen tobacco products were purchased within NYC in 2015 that did not have explicit flavour names, along with three with flavour names. These were analysed for 92 known flavour chemicals plus triacetin by gas chromatography/mass spectrometry. 14 of the 16 products had total determined flavour chemical levels that were higher (>0.3 mg/g) than in previously studied flavour-labelled products and of a chemical profile indicating added flavour chemicals. The results suggest that the tobacco industry has responded to sales restrictions by renaming flavoured products to avoid explicitly identifying them as flavoured. While chemical analysis is the most precise means of identifying flavours in tobacco products, federal tobacco laws pre-empt localities from basing regulations on that approach, limiting enforcement options. If the Food and Drug Administration would mandate that all tobacco products must indicate when flavourings are present above a specific level, local jurisdictions could enforce their sales restrictions. A level of 0.1 mg/g for total added flavour chemicals is suggested here as a relevant reference value for regulating added flavour chemicals in tobacco products. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

k{sub 0}-INAA for determining chemical elements in bird feathers

Energy Technology Data Exchange (ETDEWEB)

Franca, Elvis J., E-mail: ejfranca@usp.b [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil); Fernandes, Elisabete A.N.; Fonseca, Felipe Y. [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil); Antunes, Alexsander Z. [IF, Instituto Florestal do Estado de Sao Paulo, Rua do Horto 931, Horto Florestal 02377-000, Sao Paulo, SP (Brazil); Bardini Junior, Claudiney; Bacchi, Marcio A.; Rodrigues, Vanessa S.; Cavalca, Isabel P.O. [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil)

2010-10-11

The k{sub 0}-method instrumental neutron activation analysis (k{sub 0}-INAA) was employed for determining chemical elements in bird feathers. A collection was obtained taking into account several bird species from wet ecosystems in diverse regions of Brazil. For comparison reason, feathers were actively sampled in a riparian forest from the Marins Stream, Piracicaba, Sao Paulo State, using mist nets specific for capturing birds. Biological certified reference materials were used for assessing the quality of analytical procedure. Quantification of chemical elements was performed using the k{sub 0}-INAA Quantu Software. Sixteen chemical elements, including macro and micronutrients, and trace elements, have been quantified in feathers, in which analytical uncertainties varied from 2% to 40% depending on the chemical element mass fraction. Results indicated high mass fractions of Br (max=7.9 mg kg{sup -1}), Co (max=0.47 mg kg{sup -1}), Cr (max=68 mg kg{sup -1}), Hg (max=2.79 mg kg{sup -1}), Sb (max=0.20 mg kg{sup -1}), Se (max=1.3 mg kg{sup -1}) and Zn (max=192 mg kg{sup -1}) in bird feathers, probably associated with the degree of pollution of the areas evaluated. In order to corroborate the use of k{sub 0}-INAA results in biomonitoring studies using avian community, different factor analysis methods were used to check chemical element source apportionment and locality clustering based on feather chemical composition.

On the occurrence of metallic character in the periodic table of the chemical elements.

Science.gov (United States)

Hensel, Friedrich; Slocombe, Daniel R; Edwards, Peter P

2015-03-13

The classification of a chemical element as either 'metal' or 'non-metal' continues to form the basis of an instantly recognizable, universal representation of the periodic table (Mendeleeff D. 1905 The principles of chemistry, vol. II, p. 23; Poliakoff M. & Tang S. 2015 Phil. Trans. R. Soc. A 373: , 20140211). Here, we review major, pre-quantum-mechanical innovations (Goldhammer DA. 1913 Dispersion und Absorption des Lichtes; Herzfeld KF. 1927 Phys. Rev. 29: , 701-705) that allow an understanding of the metallic or non-metallic status of the chemical elements under both ambient and extreme conditions. A special emphasis will be placed on recent experimental advances that investigate how the electronic properties of chemical elements vary with temperature and density, and how this invariably relates to a changing status of the chemical elements. Thus, the prototypical non-metals, hydrogen and helium, becomes metallic at high densities; and the acknowledged metals, mercury, rubidium and caesium, transform into their non-metallic forms at low elemental densities. This reflects the fundamental fact that, at temperatures above the absolute zero of temperature, there is therefore no clear dividing line between metals and non-metals. Our conventional demarcation of chemical elements as metals or non-metals within the periodic table is of course governed by our experience of the nature of the elements under ambient conditions. Examination of these other situations helps us to examine the exact divisions of the chemical elements into metals and non-metals (Mendeleeff D. 1905 The principles of chemistry, vol. II, p. 23). © 2015 The Author(s) Published by the Royal Society. All rights reserved.

Characterization of chemical elements in soil submitted to different systems use and management by energy dispersive x-ray fluorescence spectrometry (EDXRF)

International Nuclear Information System (INIS)

Wastowski, Arci Dirceu; Rosa, Genesio Mario da; Cherubin, Mauricio Roberto; Rigon, Joao Paulo Gonsiorkiewicz

2010-01-01

This study aimed to evaluate the chemical elements levels in soil, submitted to different management systems and use by the Energy Dispersive X-Ray Fluorescence Spectrometry - EDXRF. The systems were T1 - agroforestry (SAF), T2 - native field (CN), T3 - native forest (NM), T4 - tillage forest (PF); T5 - conventional tillage system (SPC) and T6 - system tillage (NT). Samples were collected at 0-10 and 10-20 cm, dried and ground for analysis in EDX-720. The soil showed no difference in the average concentrations of chemical elements analyzed in the profiles, but the systems presented different concentrations of metal elements, and T3 had the highest K, Ca and Zn at 0-10 cm and higher contents of K, Ca, Cu, Zn and Mn in the layer of 10-20 cm. (author)

Chemical behaviour of transuranic elements in the natural environment

International Nuclear Information System (INIS)

Kim, J.I.

1991-01-01

The chemical behaviour of transuranic elements in natural aquifer systems is governed by a variety of geochemical reactions, such as dissolution reaction (solubility), hydrolysis, complexation with inorganics or organics, redox reaction, colloid formation, geochemical interaction with surfaces of various minerals, coprecipitation, mineralisation etc. This paper reviews the present state of knowledge on some of these particular reactions. The emphasis is placed on how the individual reactions can be appraised for the long-term prediction of the geochemical behaviour of transuranic elements in the natural environment. Of the various reactions, the primary thermodynamic processes of dissolution of transuranic compounds in aquatic solution, complexation with important anions present in groundwater and colloid generation are discussed with notable examples. Various laser spectroscopy in use for the chemical speciation are mentioned briefly as for their spectroscopic capability as well as applicability. The present review discussion is primarily directed to a better understanding of the migration behaviour of transuranic elements in natural aquifer systems. (author) 100 refs

Chemical form of transuranic elements in underground environment and its effect on adsorption

International Nuclear Information System (INIS)

Tanaka, Tomo

1990-01-01

Many of the transuranic elements such as Np, Pu and Am contained in high-level radioactive wastes are highly dangerous to humans and have extremely long lives. Therefore, safety evaluation of them is highly important after their disposal into the ground. Particularly important processes include the migration of these transuranic elements in near and far fields. The migration of a nuclide depends largely on its chemical form in the underground environment. The present report first describes various chemical forms of transuranic elements in underground environments and outlines their migration behaviors. Techniques that have recently become available for determining their chemical forms include photo-acoustic spectroscopy, thermal lensing spectroscopy, laser induced fluorescence, photo-acoustic detection of light scattering, auto-correlation photon spectroscopy, and laser-induced time-resolved spectrofluorometry. Chemical forms of these elements are then discussed focusing on underground environmental conditions, pH-Eh diagram, deposition/dissolution, formation of complex, formation of colloid, and organic complexes. Migration is discussed in relation to ions, insoluble matters, and colloids. (N.K.)

Features of adsorbed chemical elements and their isotopes distribution in iodine air filters AU-1500 of nuclear power plant

International Nuclear Information System (INIS)

Neklyudov, I.M.; Dovbnya, A.N.; Dikiy, N.P.; Ledenyov, O.P.; Lyashko, Yu.V.

2013-01-01

The main aim of research is to investigate the physical features of spatial distribution of the adsorbed chemical elements and their isotopes in the granular filtering medium in the iodine air filters of the type of AU-1500 in the forced-exhaust ventilation at the nuclear power plant. The ?-activation analysis method is applied to accurately characterize the distribution of the adsorbed radioactive chemical elements and their isotopes in the granular filtering medium in the AU-1500 iodine air filter after its long term operation at the nuclear power plant. The typical spectrum of the detected chemical elements and their isotopes in the AU-1500 iodine air filter, which was exposed by the irradiation of bremsstrahlung gamma-quantum producing by the accelerating electrons in the tantalum target, are obtained. The spatial distributions of the detected chemical element 127 I and some other chemical elements and their isotopes in the layer of absorber, which was made of the cylindrical coal granules of the type of SKT-3, in the AU-1500 iodine air filter are also researched. The possible influences by the standing wave of air pressure in the iodine air filter on the spatial distribution of the chemical elements and their isotopes in the iodine air filter are discussed. The comprehensive analysis of obtained research results on the distribution of the adsorbed chemical elements and their isotopes in the absorber of iodine air filter is performed.

On-stream chemical element monitor

International Nuclear Information System (INIS)

Averitt, O.R.; Dorsch, R.R.

1979-01-01

An apparatus and method for on-stream chemical element monitoring are described wherein a multiplicity of sample streams are flowed continuously through individual analytical cells and fluorescence analyses are performed on the sample streams in sequence, together with a method of controlling the time duration of each analysis as a function of the concomitant radiation exposure of a preselected perforate reference material interposed in the sample-radiation source path

Gas-phase chemistry of element 114, flerovium

Directory of Open Access Journals (Sweden)

Yakushev Alexander

2016-01-01

Full Text Available Element 114 was discovered in 2000 by the Dubna-Livermore collaboration, and in 2012 it was named flerovium. It belongs to the group 14 of the periodic table of elements. A strong relativistic stabilisation of the valence shell 7s27p21/2 is expected due to the orbital splitting and the contraction not only of the 7s2 but also of the spherical 7p21/2 closed subshell, resulting in the enhanced volatility and inertness. Flerovium was studied chemically by gas-solid chromatography upon its adsorption on a gold surface. Two experimental results on Fl chemistry have been published so far. Based on observation of three atoms, a weak interaction of flerovium with gold was suggested in the first study. Authors of the second study concluded on the metallic character after the observation of two Fl atoms deposited on gold at room temperature.

Platinum-group elements in southern Africa: mineral inventory and an assessment of undiscovered mineral resources: Chapter Q in Global mineral resource assessment

Science.gov (United States)

Zientek, Michael L.; Causey, J. Douglas; Parks, Heather L.; Miller, Robert J.

2014-01-01

The platinum-group elements, platinum, palladium, rhodium, ruthenium, iridium, and osmium, possess unique physical and chemical characteristics that make them indispensable to modern technology and industry. However, mineral deposits that are the main sources of these elements occur only in three countries in the world, raising concerns about potential disruption in mineral supply. Using information in the public domain, mineral resource and reserve information has been compiled for mafic and ultramafic rocks in South Africa and Zimbabwe that host most of the world’s platinum-group element resources.

Superheavy element chemistry. Achievements and perspectives

International Nuclear Information System (INIS)

Schaedel, M.

2007-01-01

Superheavy elements have been synthesized and chemically characterized one-atom-at-a-time up to element 108. Presently, the quest for element 112 is one of the hottest topics in this field. The transactinide elements 104 to 108 are members of group 4 to 8 of the Periodic Table and element 112 belongs into group 12. Chemical properties of some of these elements, like elements 104 and 105, show stunning deviations from simple extrapolations within their respective group while others exhibit great similarities with their lighter homologues elements. First experiments to investigate seaborgium (Sg, element 106) in aqueous solution were performed. Again, in large international collaborations at the GSI, several gas-phase chemistry experiments were performed with hassium (Hs, element 108). Recently, the highly efficient and very clean separation of Hs was applied for nuclear studies of various Hs nuclides investigating their cross section and their nuclear decay properties in the region of the doubly-magic 270 Hs (Z=108, N=162). To overcome certain limitations of the presently used on-line chemical separations the new TransActinide Separation and Chemistry Apparatus (TASCA) - with a gas-filled recoil separator as a front-end tool - was designed and built at the GSI in a collaborative effort. Presently in its commissioning phase, TASCA shall be a key instrument for a big leap into quantitatively and qualitatively new experiments in the region of superheavy elements. (author)

The TSCA interagency testing committee`s approaches to screening and scoring chemicals and chemical groups: 1977-1983

Energy Technology Data Exchange (ETDEWEB)

Walker, J.D. [Environmental Protection Agency, Washington, DC (United States)

1990-12-31

This paper describes the TSCA interagency testing committee`s (ITC) approaches to screening and scoring chemicals and chemical groups between 1977 and 1983. During this time the ITC conducted five scoring exercises to select chemicals and chemical groups for detailed review and to determine which of these chemicals and chemical groups should be added to the TSCA Section 4(e) Priority Testing List. 29 refs., 1 fig., 2 tabs.

Fractionation of chemical elements including the REEs and 226Ra in stream contaminated with coal-mine effluent

International Nuclear Information System (INIS)

Centeno, L.M.; Faure, G.; Lee, G.; Talnagi, J.

2004-01-01

Water draining from abandoned open-pit coal mines in southeastern Ohio typically has a low pH and high concentrations of Fe, Al and Mn, as well as of trace metals (Pb, Cu, Zn, Ni, Co, etc.) and of the rare earth elements (REEs). The cations of different elements are sorbed selectively by Fe and Al hydroxide precipitates which form with increasing pH. As a result, the trace elements are separated from each other when the hydroxide precipitates are deposited in the channel of a flowing stream. Therefore, the low-energy environment of a stream contaminated by mine effluent is a favorable site for the chemical fractionation of the REEs and of other groups of elements with similar chemical properties. The interpretation of chemical analyses of water collected along a 30-km-stretch of Rush Creek near the town of New Lexington, Perry County, Ohio, indicates that the abundances of the REEs in the water appear to change downstream when they are normalized to the REE concentrations of the mine effluent. In addition, the Ce/La ratios (and those of all REEs) in the water decrease consistently downstream. The evidence indicates that the REEs which remain in solution are enriched La and Ce because the other REEs are sorbed more efficiently. The solid Fe(OH) 3 precipitates in the channel of Rush Creek upstream of New Lexington also contain radioactive 226 Ra that was sorbed from the water. This isotope of Ra is a decay product of 238 U which occurs in the Middle Pennsylvanian (Upper Carboniferous) coal and in the associated shale of southeastern Ohio. The activity of 226 Ra of the Fe(OH) 3 precipitates increases with rising pH, but then declines farther downstream as the concentration of Ra remaining in the water decreases

Chemical elements dynamic in the fermentation process of ethanol producing

International Nuclear Information System (INIS)

Nepomuceno, N.; Nadai Fernandes, E.A. de; Bacchi, M.A.

1994-01-01

This paper provides useful information about the dynamics of chemical elements analysed by instrumental neutron activation analysis (INAA) and, found in the various segments of the fermentation process of producing ethanol from sugar cane. For this, a mass balance of Ce, Co, Cs, Eu, Fe, Hf, La, Sc, Sm, and Th, terrigenous elements, as well as Br, K, Rb, and Zn, sugar cane plant elements, has been demonstrated for the fermentation vats in industrial conditions of ethanol production. (author). 10 refs, 4 figs, 1 tab

Concentration and measuring Platinum Group Elements (PGE) Transfer Factor in soil and vegetations

International Nuclear Information System (INIS)

Adibah Sakinah Oyub

2012-01-01

This study was conducted to determine the concentration and to measure platinum group elements (PGE) transfer factor in environmental samples of roadside soil and vegetation. The use of vehicle catalytic converter has released platinum group elements (PGE) and other gases into the environment. Thus, roadside soil and plants were exposed to this element and has become the medium for the movement of this elements. Samples of roadside soil and vegetation were taken at various locations in UKM Bangi Toll and the concentration of platinum group elements (PGE) is determined using mass spectrometry-inductively coupled plasma (ICP-MS). Overall, the concentrations of platinum group elements (PGE), which is the element platinum (Pt) in soil was 0.016 ± 0.036 μgg -1 . While the concentration of the elements palladium (Pd) was 0.079 ± 0.019 μgg -1 and element rhodium (Rh) is at a concentration of 0.013 ± 0.020 μgg -1 . Overall, the transfer factor for the element platinum (Pt) is 1. While the transfer factor of the element palladium (Pd) is 0.96 and the element rhodium (Rh) is 1.11. In conclusion, the concentration of platinum group elements (PGE) in soils have increased. (author)

Solution of two energy-group neutron diffusion equation by triangular elements

International Nuclear Information System (INIS)

Correia Filho, A.

1981-01-01

The application of the triangular finite elements of first order in the solution of two energy-group neutron diffusion equation in steady-state conditions is aimed at. The EFTDN (triangular finite elements in neutrons diffusion) computer code in FORTRAN IV language is developed. The discrete formulation of the diffusion equation is obtained applying the Galerkin method. The power method is used to solve the eigenvalues' problem and the convergence is accelerated through the use of Chebshev polynomials. For the equation systems solution the Gauss method is applied. The results of the analysis of two test-problems are presented. (Author) [pt

Method to determine trace elements in water samples by neutron activation analysis

International Nuclear Information System (INIS)

Kueppers, G.; Erdtmann, G.

1981-05-01

For the determination of trace elements in water by neutron activation analysis irradiation porcedures and chemical separation procedures have been developed. Irradiation in melted quarz glass ampoules in the presence of a platinum wire (for recombination of the oxyhydrogen gas produced by radiolysis) proved successfull with different variants of the irradiation methods, as long irradiation periods without pressure build-up could be achieved. Possible falsifications of the analysis results were investigated in detail (losses by absorption on vessel walls etc.). The irradiated samples can be measured directly with a gamma ray spectrometer and from the radionuclides found the trace element contents may be calculated. More sensitive determinations are possible if the radionuclides are chemically separated. Procedures for removing the matrix activities, for the separation of the radionuclides in groups of elements and for the isolation of single elements have been developed. For especially sensitive determination of some elements selective separation procedures for antimony, cadmium, selenium, mercury and uranium have been developed. The analytical procedures described have been applied to trace element determinations in river water, glacier ice and water solutions from technical processes. (orig./RB) [de

Some chemical elements in gamma irradiated adults of the mediterranean fruit fly , Ceratitis Capitata (WIED.)

International Nuclear Information System (INIS)

El-akhdar, E.A.H.

2005-01-01

The chemical analysis of the elemental compositions of both males and females of the Mediterranean fruit fly, Ceratitis capitata (Wied.), was conducted on adult flies irradiated in the full grown pupae with 50, 70, 90 and 110 Gray at different ages (newly emerged, 7 and 15 days old). The data revealed the presence of ten elements, three of which are major (Na, K and N), four are moderate (P, Ca, Fe and Mg) and three are minors (Zn, Mn and Cu). Their quantities, however, varied according to adult sex, age and radiation dose. In all cases, the major elements remained major, the moderate elements remained moderate and the minor elements remained minor although the elements of each group differed in their arrangement according to changes in their quantities

The Superheavy Elements and Anti-Gravity

International Nuclear Information System (INIS)

Anastasovski, Petar K.

2004-01-01

The essence of any propulsion concept is to overcome gravity. Anti-gravity is a natural means to achieve this. Thus, the technology to pursue anti-gravity, by using superheavy elements, may provide a new propulsion paradigm. The theory of superluminal relativity provides a hypothesis for existence of elements with atomic number up to Z = 145, some of which may possess anti-gravity properties. Analysis results show that curved space-time exists demonstrating both gravitic and anti-gravitic properties not only around nuclei but inside the nuclei as well. Two groups of elements (Z < 64 and 63 < Z <145) exist that demonstrate these capabilities. The nuclei of the first group of elements have the masses with only the property of gravity. The nuclei of the elements of the second group have the masses with both properties: gravity and anti-gravity in two different ranges of curved space-time around the nuclei.. The hypothetical element with Z = 145 is the unique among all elements whose nucleus has only anti-gravity property. It is proposed that this element be named Hawking, in honour of Stephen W. Hawking

Black poplar-tree (Populus nigra L.) bark as an alternative indicator of urban air pollution by chemical elements

International Nuclear Information System (INIS)

Berlizov, A.N.; Malyuk, I.A.; Tryshyn, V.V.

2008-01-01

Capabilities of black poplar-tree (Populus nigra L.) bark as a biomonitor of atmospheric air pollution by chemical elements were tested against epiphytic lichens Xanthoria parietina (L.) and Physcia adscendens (Fr.). Concentrations of 40 macro and trace elements were determined using epicadmium and instrumental NAA. The data obtained were processed using non-parametric tests. A good correlation was found between concentrations of majority of elements in bark and lichens. On the accumulation capability bark turned out to be competitive with both lichens examined. The main inorganic components of black poplar-tree bark were revealed. A substrate influence on the concentrations of some elements in epiphytic lichens was established. An optimized procedure of bark pre-irradiation treatment was suggested. (author)

Platinum-group element mineralization

International Nuclear Information System (INIS)

Gruenewaldt, G.

1985-01-01

The purpose of this investigation is to determine the geological processes responsible for the abnormal enrichment of the platinum-group elements (PGE) in the mineralized layers of the Bushveld Complex. Questions asked are: what processes caused enrichment of the Bushveld magma in the PGE ; by what processes were these PGE concentrated in the mineralized layers ; was contamination of the Bushveld magma from external sources important in the formation of the PGE enriched layers ; what are the effects of fractional crystallization on the PGE ratios

Correlation study of chemical elements in phosphate ores

International Nuclear Information System (INIS)

Braganca, Maura Julia Camara da Silva

1999-07-01

Geological phenomena, 1) endogenous (volcanism, magmatic flow, metasomatism); 2) metamorphic (resultant of action of high temperature and pressure) and; 3) exogenous (intemperism, contamination) can modify the chemical composition of rocks soils. Thus, chemical elements with little mobility can be used as indicators of the previous geological situation before the occurrence of these phenomena and can sign the chemical composition of the initial formation. The elements with great mobility can already be used as indicators of the characteristic and intensity of the changes, can point out the influence factors and its space and time conditions. In this work the results of the study of phosphated samples ores coming from two alkaline-carbonatitic chimneys (Araxa and Catalao) and from a meta sedimentary rock (Patos de Minas), located phosphate rock deposit, are presented. The results were obtained using the instrumental neutron activation analysis, inductively coupled plasma-mass spectrometry (ICP-MS) and ICP-AES techniques. A comparison of the three types of samples ores, using chemical, crystallographic and statistical methods, shows that the Araxa and Catalao present some geochemical similarities and they are distinguished of Patos de Minas, despite its geographic proximity. (author)

INVESTIGATION OF BRAND NAME-COUNTRY OF ORIGIN PREFERENCE IN FOUR DIFFERENT PRODUCT GROUPS WITH RESPECT TO CONSPICUOUS CONSUMPTION TENDENCY

Directory of Open Access Journals (Sweden)

Volkan Doğan

2013-10-01

Full Text Available The aim of this study is to examine different preferences for brand name–country of origin shaped in line with levels of conspicuous consumption tendency and to determine Turkish consumers’ preferences for brand name–country of origin combinations in different product groups. The study was conducted in Eskisehir (Turkey with a sample of 413 people chosen through convenience sampling. The study data were collected with a questionnaire and face-face-to interviews. The participants’ preferences for brand name-country of origin combinations were determined separately based on four different product groups(hedonic, utilitarian, durable and non-durable. The study showed that, for all the four product groups, the participants preferred the products with a Turkish brand name and Turkey as the country of origin most, followed by the products with a French brand name and France as the country of origin. This finding suggests that, with respect to the four product groups in the study, Turkish consumers preferred domestic products over foreign products. Also, the participants who preferred French brand name-France as the country of origin for the hedonic product, French brand name-Turkey as the country of origin for the utilitarian product, French brand name-Turkey as the country of origin for the durable product and French brand name-France as the country of origin for the non-durable product were found to have highest tendency of conspicuous consumption in the corresponding product groups. In other words, as the level of conspicuous consumption increased, the participants tended to prefer French brand name-France as the country of origin for the hedonic product, French brand name-Turkey as the country of origin for the utilitarian product, French brand name-Turkey as the country of origin for the durable product and French brand name-France as the country of origin for the non-durable product.

The distributions of chemical elements and Caesium-137 in the Northern-Crimean canal ecosystem

International Nuclear Information System (INIS)

Lazorenko, G.

1998-01-01

The distributions in 1992-1995 of some chemical elements and 137 Cs concentrations in components of the Northern-Crimean Canal (NCC) ecosystem and agricultural fields of the Kherson District and the Northern Crimea irrigated by the Dnieper River water are presented in the work. Five main sampling were selected between the Kakhovka Reservior (at the beginning of the NCC) and the Karkinitsky Bay along the 150 km of the main Canal. Two additional stations were selected in discharge canals to study of the role of irrigated agricultural fields in the accumulation of 137 Cs and chemical elements from water. (author)

Multielement analysis of reagents used in chemical identification of transuranic elements

International Nuclear Information System (INIS)

Montalvan Estrada, A.; Brigido Flores, O.; Maslov, O.D.; Dmitriev, S.N.

2006-01-01

For more than 40 years, chemical identification of transuranic elements has been used at the Laboratory of Nuclear Reactions of the Join Institute for Nuclear Research, Dubna, Russia, as a secondary method of identification. Chlorination of transuranic elements obtained by nuclear reactions is an important step of the procedure in order to obtain volatile compounds able to pass through a thermo chromatographic process. To access the quality of the reagents TiCl 4 and SOCl 2 multielement analysis was carried out using both X-rays fluorescence and gamma activation. It was followed the simplest procedure for reagents samples pretreatment, so further interferences from other chemical products were avoided. X-rays fluorescence analysis was performed in a spectrometer with Si(Li) detector with a resolution for Fe (K?) of 190 eV. Both Cd-109 and Am-241 were used as isotopic sources of excitation. Gamma activation analysis was carried out using the compact electron accelerator MT-25, where gamma rays are produced in a stopping target. Among the parameters of the MT-25 are the following: energy range-10-25 MeV, gamma-ray flux-10 14 photon/s, power consumption-20 kw. Measurements of the induced activity were performed with the help of a HPGe detector, thin and coaxial Ge(Li) detectors. There were identified two elements in SOCl 2 -Nickel (3*10 -6 g/g) and Antimony (2*10 -7 g/g), while there were identified three elements in TiCl 4 - Zirconium (8*10 -7 g/g), Arsenic (9*10 -7 g/g) and Antimony (5*10 -7 g/g). Only five elements were detected in trace concentrations in the two analyzed reagents, that is for more than 57 elements capable of being detected using gamma activation analysis with the MT-25 only 5 had concentrations above the detection limits of the method. Not being chemical analogs of the synthesized transuranic elements (Z-104 and 106) and not being able to alpha or fission disintegrations there is not expected any interference from them in the chemical

Chemical elements in egg shell of a commercial strain of domestic ...

African Journals Online (AJOL)

A study was conducted to determine the chemical elements of the egg shell of exotic commercial pullets (Lohmann) in their first laying year. A total of 160 eggs from eighty pullets were randomly selected at three-monthly intervals during the production year for the ddermination of chemical elements or the eggshell.

INAA application in the assessment of chemical element mass fractions in adult and geriatric prostate glands

International Nuclear Information System (INIS)

Zaichick, Vladimir; Zaichick, Sofia

2014-01-01

The variation with age of the mass fraction of 37 chemical elements in intact nonhyperplastic prostate of 65 healthy 21–87 year old males was investigated by instrumental neutron activation analysis with high resolution spectrometry of short- and long-lived radionuclides. Mean values (M±SΕΜ) for mass fractions (mg kg −1 , dry mass basis) of the chemical elements studied were: Ag—0.055±0.007, Br—33.2±3.3, Ca—2150±118, Cl—13014±703, Co—0.038±0.003, Cr—0.47±0.05, Fe—99.3±6.1, Hg—0.044±0.006, K—11896±356, Mg—1149±68, Mn—1.41±0.07, Na—10886±339, Rb—12.3±0.6, Sb—0.049±0.005, Sc—0.021±0.003, Se—0.65±0.03, and Zn—795±71. The mass fraction of other chemical elements measured in this study were lower than the corresponding detection limits (mg kg −1 , dry mass basis): As<0.1, Au<0.01, Ba<100, Cd<2, Ce<0.1, Cs<0.05, Eu<0.001, Gd<0.02, Hf<0.2, La<0.5, Lu<0.003, Nd<0.1, Sm<0.01, Sr<3, Ta<0.01, Tb<0.03, Th<0.05, U<0.07, Yb<0.03, and Zr<0.3. This work revealed that there is a significant trend for increase with age in mass fractions of Co (p<0.0085), Fe (p<0.037), Hg (p<0.035), Sc (p<0.015), and Zn (p<0.0014) and for a decrease in the mass fraction of Mn (p<0.018) in prostates, obtained from young adult up to about 60 years, with age. In the nonhyperplastic prostates of males in the sixth to ninth decades, the magnitude of mass fractions of all chemical element were maintained at near constant levels. Our finding of correlation between the prostatic chemical element mass fractions indicates that there is a great variation of chemical element relationships with age. - Highlights: • 37 trace elements were determined in prostate of 65 healthy 21–87 year old males by NAA. • Co, Fe, Hg, Sc, and Zn contents significantly increase with age. • Mn content significantly decreases with age. • All elemental contents in the sixth to ninth decades are near constant level. • There is a great disturbance of chemical element

Results of the Experiment on Chemical Identification of Db as a Decay Product of Element 115

CERN Document Server

Dmitriev, S N; Utyonkov, V K; Shishkin, S V; Eremin, A V; Lobanov, Yu V; Tsyganov, Yu S; Chepigin, V I; Sokol, E A; Vostokin, G K; Aksenov, N V; Hussonnois, M; Itkis, M G; Aggeler, H W; Schumann, D; Bruchertseifer, H; Eichler, R; Shaughnessy, D A; Wilk, P A; Kenneally, J M; Stoyer, M A; Wild, J F

2004-01-01

For the first time the chemical identification of Db as the terminal isotope of the decay element 115 produced via the $^{243}{\\text{Am}}(^{48}{\\text{Ca}},3n)^{288}115$ reaction was realized. The experiment was performed on the U400 cyclotron of FLNR, JINR. The $^{243}$Am target was bombarded with a beam dose of $3.4\\cdot 10^{18}$ $^{48}$Ca projectiles at an energy of 247 MeV in the center of the target. The reaction products were collected in the surface of a copper catcher block, which was removed with a lathe and then dissolved in concentrated HNO$_3$. The group 5 elements were separated by sorption onto Dowex 50$\\times$8 cation-exchange resin with subsequent desorption using 1M HF, which forms anionic fluoride complexes of group 5 elements. The eluant was evaporated onto 0.4 $\\mu$m thick polyethylene foils which were placed between a pair of semiconductor detectors surrounded by $^3$He neutron counters for measurement of $\\alpha$ particles, fission fragments and neutrons. Over the course of the experiment...

Describing of elements IO field in a testing computer program

Directory of Open Access Journals (Sweden)

Igor V. Loshkov

2017-01-01

Full Text Available A standard of describing the process of displaying interactive windows on a computer monitor, through which an output of questions and input of answers are implemented during computer testing, is presented in the article [11]. According to the proposed standard, the description of the process mentioned above is performed with a format line, containing element names, their parameters as well as grouping and auxiliary symbols. Program objects are described using elements of standard. The majority of objects create input and output windows on a computer monitor. The aim of our research was to develop a minimum possible set of elements of standard to perform mathematical and computer science testing.The choice of elements of the standard was conducted in parallel with the development and testing of the program that uses them. This approach made it possible to choose a sufficiently complete set of elements for testing in fields of study mentioned above. For the proposed elements, names were selected in such a way: firstly, they indicate their function and secondly, they coincide with the names of elements in other programming languages that are similar by function. Parameters, their names, their assignments and accepted values are proposed for the elements. The principle of name selection for the parameters was the same as for elements of the standard: the names should correspond to their assignments or coincide with names of similar parameters in other programming languages. The parameters define properties of objects. Particularly, while the elements of standard create windows, the parameters define object properties (location, size, appearance and the sequence in which windows are created. All elements of standard, proposed in this article are composed in a table, the columns of which have names and functions of these elements. Inside the table, the elements of standard are grouped row by row into four sets: input elements, output elements, input

Chemical characterization of archaeological ceramics fragments by X-ray (μ-XRF) micro fluorescence

International Nuclear Information System (INIS)

Silva, Richard Maximiliano da Cunha e; Nascimento Filho, Virgilio Franco do; Appoloni, Carlos Roberto; Perez, Carlos Alberto

2002-01-01

The concentrations of the inorganic chemical elements presents in archaeological ceramic samples and clay samples allows the study about the clay sources determination used in the ceramic production. The analyzed samples are fragments of Brazilian indigenous ceramic, found in the area of the city of Londrina, North of Parana, and they belong to the archaeological collection of the 'Padre Carlos Weiss' Historical Museum, of the State University of Londrina. The determination of the chemical elements in these fragments was performed by energy dispersive X-ray microfluorescence (μ-XRF), for being not destructive and multielementar. The analytic technique allowed the identification of the K, Ca, Ti, Mn, Fe minority elements, and the Cr, Ni, Cu, Zn and Rb trace elements. The cluster analysis for the method of the medium grouping was used, and it was obtained two different groups, taking to conclude that indigenous Tupiguaranis used two clay sources in the making of its ceramic. (author)

A Kine-chemical Investigation of the AB Dor Moving Group "Stream"

Science.gov (United States)

Barenfeld, Scott A.; Bubar, Eric J.; Mamajek, Eric E.; Young, Patrick A.

2013-03-01

The AB Dor Moving Group consists of a "nucleus" of ~10 stars at d ~= 20 pc, along with dozens of purported "stream" members distributed across the sky. We perform a chemical and kinematic analysis of a subsample of AB Dor stream stars to test whether they constitute a physical stellar group. We use the NEMO Galactic kinematic code to investigate the orbits of the stream members, and perform a chemical abundance analysis using high resolution spectra taken with the Magellan Clay 6.5 m telescope. Using a χ2 test with the measured abundances for 10 different elements, we find that only half of the purported AB Dor stream members could possibly constitute a statistically chemically homogeneous sample. Some stream members with three-dimensional velocities were hundreds of parsecs from the AB Dor nucleus ~108 yr ago, and hence were unlikely to share a common origin. We conclude that the published lists of AB Dor moving group stream members are unlikely to represent the dispersed remnant of a single star formation episode. A subsample of the stream stars appears to be both statistically chemically homogeneous and in the vicinity of the AB Dor nucleus at birth. Their mean metallicity is [Fe/H] = 0.02 ± 0.02 dex, which we consider representative for the AB Dor group. Finally, we report a strong lower limit on the age of the AB Dor nucleus of >110 Myr based on the pre-main sequence contraction times for K-type members which have reached the main sequence.

Seasonal variations in the concentration and solubility of elements in atmospheric particulate matter: a case study in Northern Italy

Directory of Open Access Journals (Sweden)

Canepari S.

2013-04-01

Full Text Available Atmospheric particulate matter is characterized by a variety of chemical components, generally produced by different sources. Chemical fractionation of elements, namely the determination of their extractable and residual fractions, may reliably increase the selectivity of some elements as tracers of specific PM sources. Seasonal variations of atmospheric particulate matter concentration in PM10 and PM2.5, of elemental concentration in PM10 and PM2.5, of the extractable and residual fraction of elements in different size fractions in the range 0.18 – 18 μm are reported in this paper. The effect of the ageing of the air masses is discussed.

Platinum-group elements in the Eastern Deccan volcanic province ...

Indian Academy of Sciences (India)

This study is the first detailed investigation of the platinum-group elements (PGE) at the eastern mar- ... A Zr vs. Pd scattergram found a strong positive correlation for these two elements ..... and the PGE and Au collected by co-precipitation.

Single electron detachment of carbon group and oxygen group elements incident on helium

International Nuclear Information System (INIS)

Huang Yongyi; Li Guangwu; Gao Yinghui; Yang Enbo; Gao Mei; Lu Fuquan; Zhang Xuemei

2006-01-01

The absolute single electron detachment (SED) cross sections of carbon group elements C - , Si - , Ge - in the energy range of 0.05-0.29 a.u. (5 keV-30 keV) and oxygen group elements O - and S - 0.08-0.27 a.u. (5 keV-30 keV), incident on helium are measured with growth rate method. In our energy region, the SED cross sections of C - , Si - , S - and Ge - increase with the projectiles velocity, at the same time, O - cross sections reach a conspicuous maximum at 0.18 a.u. Some abnormal behavior occurs in measurement of SED cross sections for the oxygen group collision with helium. Our results have been compared with a previous work

Quality in the chemical analysis of biological matrices by fluorescence X-ray by energy dispersive

International Nuclear Information System (INIS)

Sousa, Evely E. de; Paiva, Jose Daniel S. de; Franca, Elvis J. de; Almeida, Macio E.S.; Cantinha, Rebeca S.; Hazin, Clovis A.

2013-01-01

The aim of this study was to obtain multielement analytical curves of high analytical rigor to the analysis of biological matrices by the technique of fluorescence x-ray energy dispersive - EDXRF. Calibration curves were constructed from the reference materials IAEA 140, IAEA 155, IAEA V8, V10 to the International Atomic Energy Agency - IAEA, and SRM1515, SRM 1547, SRM 1570a, SRM 1573a, SEM 1567a, to the National Institute of Standards and Technology - NIST. After energy calibration, all samples were subjected to vacuum to the analyzes by 100 seconds for each group of chemical elements. The voltages used were respectively 15 keV for chemical elements with less than atomic number 22 and 50 keV for the others. After the construction of the curves, the analytical quality was assessed by the analysis of a portion-test of the reference material SRM 2976, also produced by NIST. Based on the number of certified reference materials used for construction of calibration curves in this work, quality analytical protocol was originated with considerable reliability for quantification of chemical elements in biological samples by EDXR

The Natural Selection of the Chemical Elements (by R. J. P. Williams and J. J. R. Fraústo da Silva)

Science.gov (United States)

Kauffman, George B.

1998-12-01

Clarendon: New York, 1996. xxvi + 646 pp. Figs., tables. 20.5 x 25.6 cm. ISBN 0-19-855843-0. $80.00. R. J. P. Williams, Royal Society Research Professor Emeritus at Wadham College, Oxford University, and J. J. R. Fraústo da Silva, Professor of Analytical Chemistry at the Instituto Superior Técnico, Universidade Técnica de Lisboa, have collaborated on two previous volumes: New Trends in Bio-inorganic Chemistry (1978) and The Biological Chemistry of the Elements (3rd printing, 1994). Their latest collaborative effort is a book whose ambitious objective is "to show the relationship of every kind of material around us, living and nonliving, to the properties of the chemical elements of the periodic table." The "natural selection" of the chemical elements results from a number of factors, all of which are described in detail. Among these are chemical affinity related to the electronic configuration of their atoms, thermodynamic and kinetic stability, and "functional value to an organisation such as a living system". The physicist's approach to material through phase structure and the phase rule is stressed rather than the chemist's approach through bonding theories. The entire book possesses a strong environmental and interdisciplinary emphasis.

Chemical composition and mineral elements of edible insects (at ...

African Journals Online (AJOL)

The Chemical Composition and Mineral Elements of two edible insects' larvae and termite soldiers were assayed. Their ash content were between 1.01% and 7.50%. The legless larva (LS) had 28.52% fat, while the solider ant had 7.14% and the Legged larva (LG) had 1.50%. The white ant (SA) had 15.61% protein while ...

Use of chemical elements of 1A family by tropical tree species; Uso de elementos quimicos da familia 1A por especies arboreas tropicais

Energy Technology Data Exchange (ETDEWEB)

Carmo, Andrius M.J.; Paiva, Jose Daniel S. de; Magalhaes, Marcelo R.L. de; Franca, Elvis J. de; Hazin, Clovis A., E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Bacchi, Marcio A.; Fernandes, Elisabete A.N., E-mail: mabacchi@cena.usp.br [Centro de Energia Nuclear na Agricultura (CENA/USP), Piracicaba, SP (Brazil).

2013-07-01

This study aims to evaluate the distribution of K, Rb and Cs in leaves of trees of the Atlantic Forest through studies of correlation between the chemical elements. For this, we used the Instrumental Neutron Activation Analysis for the quantification of the chemical elements. The concentration ranges found were 6700-24000 mg / kg for K, 16 to 72mg / kg for Rb and 0.08 to 0,92mg / kg for Cs. As Rb has chemical similarity to K, is easily absorbed by plants, leading to a high value (0.9) of the Pearson correlation. For the correlation between K and Cs, no significant values were detected except for some species of the Myrtaceae family. However, average correlations (0.6 and Cs by plants showed great complexity in the distribution of chemical elements in the ecosystem.

On-line gas chromatographic studies of rutherfordium (Element 104), hahnium (Element 105), and homologs

International Nuclear Information System (INIS)

Kadkhodayan, B.

1993-05-01

Gas-phase isothermal chromatogaphy is a method by which volatile compounds of different chemical elements can be separated according to their volatilities. The technique, coupled with theoretical modeling of the processes occurring in the chromatogaphy column, provides accurate determination of thermodynamic properties (e.g., adsorption enthalpies) for compounds of elements, such as the transactinides, which can only be produced on an atom-at-a-time basis. In addition, the chemical selectivity of the isothermal chromatogaphy technique provides the decontamination from interfering activities necessary for the determination of the nuclear decay properties of isotopes of the transactinide elements. Volatility measurements were performed on chloride species of Rf and its group 4 homologs, Zr and Hf, as well as Ha and its group 5 homologs, Nb and Ta. Adsorption enthalpies were calculated for all species using a Monte Carlo code simulation based on a microscopic model for gas thermochromatography in open columns with laminar flow of the carrier gas. Preliminary results are presented for Zr- and Nb-bromides

Chemical aspects of pellet-cladding interaction in light water reactor fuel elements

International Nuclear Information System (INIS)

Olander, D.R.

1982-01-01

In contrast to the extensive literature on the mechanical aspects of pellet-cladding interaction (PCI) in light water reactor fuel elements, the chemical features of this phenomenon are so poorly understood that there is still disagreement concerning the chemical agent responsible. Since the earliest work by Rosenbaum, Davies and Pon, laboratory and in-reactor experiments designed to elucidate the mechanism of PCI fuel rod failures have concentrated almost exclusively on iodine. The assumption that this is the reponsible chemical agent is contained in models of PCI which have been constructed for incorporation into fuel performance codes. The evidence implicating iodine is circumstantial, being based primarily upon the volatility and significant fission yield of this element and on the microstructural similarity of the failed Zircaloy specimens exposed to iodine in laboratory stress corrosion cracking (SCC) tests to cladding failures by PCI

Fates of Chemical Elements in Biomass during Its Pyrolysis.

Science.gov (United States)

Liu, Wu-Jun; Li, Wen-Wei; Jiang, Hong; Yu, Han-Qing

2017-05-10

Biomass is increasingly perceived as a renewable resource rather than as an organic solid waste today, as it can be converted to various chemicals, biofuels, and solid biochar using modern processes. In the past few years, pyrolysis has attracted growing interest as a promising versatile platform to convert biomass into valuable resources. However, an efficient and selective conversion process is still difficult to be realized due to the complex nature of biomass, which usually makes the products complicated. Furthermore, various contaminants and inorganic elements (e.g., heavy metals, nitrogen, phosphorus, sulfur, and chlorine) embodied in biomass may be transferred into pyrolysis products or released into the environment, arousing environmental pollution concerns. Understanding their behaviors in biomass pyrolysis is essential to optimizing the pyrolysis process for efficient resource recovery and less environmental pollution. However, there is no comprehensive review so far about the fates of chemical elements in biomass during its pyrolysis. Here, we provide a critical review about the fates of main chemical elements (C, H, O, N, P, Cl, S, and metals) in biomass during its pyrolysis. We overview the research advances about the emission, transformation, and distribution of elements in biomass pyrolysis, discuss the present challenges for resource-oriented conversion and pollution abatement, highlight the importance and significance of understanding the fate of elements during pyrolysis, and outlook the future development directions for process control. The review provides useful information for developing sustainable biomass pyrolysis processes with an improved efficiency and selectivity as well as minimized environmental impacts, and encourages more research efforts from the scientific communities of chemistry, the environment, and energy.

Chemical portioning and speciation of some trace elements in soil and street dust from Khartoum state, Sudan

International Nuclear Information System (INIS)

Ahmed, Amel Yousif

2000-09-01

In this study, surface soil and street dust samples were collected from Khartoum State, from areas exposed to industrial and traffic emission and from areas expected to be free from elemental emission to serve as control. Samples were digested using wet digestion method to determine the total concentration of Na, K, Cr, Mn, Fe, Cu, Zn and Pb using Atomic Absorption spectrophotometer (Aas), X-Ray fluorescence and flame photometer. Also samples were chemically fractionated using chemical specification method, and the solutions analyzed using Aas to determine the chemical form of the elements. Quality assurance of the data was achieved through the analysis of certified reference material. The range of the total concentration for Na, K, Mn, Fe, Cu, Zn and Pb are 400-5175, 220-4690, 0.07-315.25, 20-250, 2050.8-46000, 0.5-2305, 4.5-280, 9.5-6200 mg/kg respectively. results obtained agree with expected emission profile as inferred from the emitting source locations. Distribution of elements from emitting source locations and control samples in different chemical fractions was carried out, and the findings reinforced by enrichment factors calculations as well by the results obtained by statistical multi-variate analysis methods such as principle compared with previous literature.(Author)

Rare Earth and other Chemical Elements Accumulation in Vines of Fogo Island (Cape Verde)

Science.gov (United States)

Marques, Rosa; Prudêncio, Maria Isabel; Rocha, Fernando; Dias, Maria Isabel; Franco, Dulce

2017-04-01

The Fogo Island is the fourth bigger island of the Cape Verde (central Atlantic Ocean). This archipelago is located 570 kilometres off the coast of West Africa, and is characterized by a semi-arid climate. The volcanic soils of the caldera of this island, with an active volcanism during historical times, have been used for viticulture. The study of uptake of chemical elements by vines - absorption and translocation to grapes - grown in soils developed on alkaline pyroclasts is the main goal of this work. The concentrations of 27 chemical elements in bark, leafs and grapes of two vines, as well as in the corresponding soils ( 50). The bioavailable fraction of Cr and As in these soils may be due to the low percentage of iron oxides (particularly in the form of nanoparticles), which play an important role in the retention of these elements. The factors responsible for the phytoavailability of Sb in soils and its uptake by plants it's still poorly known. Although the Sb concentrations in earth's crust are low, higher concentrations of this element in soils may be related with hydrothermal and volcanic processes. Also, the temperature may influence the accumulation of Sb in plants, with an increase of the Sb uptake by plants at higher temperatures, due to an increased desorption rate of Sb from soil particles. Concerning U, its mobility and dispersion in soils is controlled by its oxidation state, its adsorption capacity in clay minerals or iron oxides, and the ability to form more or less soluble complexes. Although U concentrations in these volcanic soils are low, there is a fraction available for absorption and accumulation by grapes. Concerning the rare earth elements (REE), it should be noted that the light REE are not enriched in any part of the vines studied, and only the heavy REE are enriched in grapes (EF = 20-50); this can be explained by the preferential uptake of the heavy REE, after primary minerals breakdown and the formation of more soluble compounds

The use of x-ray fluorescence in the detection of inorganic elements in medicines drugs

International Nuclear Information System (INIS)

Freitas, Tatiana Pereira da Silva de; Ricci Junior, Eduardo; Zucchi, Orgheda Luiza Araujo Domingues

1997-01-01

Based on the instrumental wavelength dispersive X-ray fluorescence technique of analysis (W D-X R F), the inorganic elements in four samples of commercial medicines drugs were analyzed. The samples were used without any chemical separation of the elements or chemical pre-treatment. Eleven elements could be identified, namely Si, P, S, Cl, K, Ca, Ti, Mn, Fe, Cu and Zn. However, Si, Ti and Mn have not been mentioned in the printed instructions for the use of the medicines drugs by the producers. (author)

Multi trace element analysis of dry biological materials by neutron activation analysis including a chemical group separation

International Nuclear Information System (INIS)

Weers, C.A.

1980-07-01

Multi-element analysis of dry biological material by neutron activation analysis has to include radiochemical separation. The evaporation process is described in terms of the half-volume. The pretreatment of the samples and the development of the destruction-evaporation apparatus are described. The successive adsorption steps with active charcoal, Al 2 O 3 and coprecipitation with Fe(OH) 3 are described. Results obtained for standard reference materials are summarized. (G.T.H.)

Real Elements and p-Nilpotence of Finite Groups

Directory of Open Access Journals (Sweden)

Adolfo Ballester-Bolinches

2016-12-01

Full Text Available Our first main result proves that every element of order 4 of a Sylow 2-subgroup S of a minimal non-2-nilpotent group G, is a real element of S. This allows to give a character-free proof of a theorem due to Isaacs and Navarro (see [9, Theorem B]. As an application, the authors show a common extension of the p-nilpotence criteria proved in [3] and [9].

The Relationship Between Confrontation Naming and Story Gist Production in Aphasia.

Science.gov (United States)

Richardson, Jessica D; Dalton, Sarah Grace; Fromm, Davida; Forbes, Margaret; Holland, Audrey; MacWhinney, Brian

2018-03-01

The purpose of this study was to examine the relationship between picture naming performance and the ability to communicate the gist, or essential elements, of a story. We also sought to determine if this relationship varied according to Western Aphasia Battery-Revised (WAB-R; Kertesz, 2007) aphasia subtype. Demographic information, test scores, and transcripts of 258 individuals with aphasia completing 3 narrative tasks were retrieved from the AphasiaBank database. Narratives were subjected to a main concept analysis to determine gist production. A correlation analysis was used to investigate the relationship between naming scores and main concept production for the whole group of persons with aphasia and for WAB-R subtypes separately. We found strong correlations between naming test scores and narrative gist production for the large sample of persons with aphasia. However, the strength of the correlations varied by WAB-R subtype. Picture naming may accurately predict gist production for individuals with Broca's and Wernicke's aphasia, but not for other WAB-R subtypes. Given the current reprioritization of outcome measurement, picture naming may not be an appropriate surrogate measure for functional communication for all persons with aphasia. https://doi.org/10.23641/asha.5851848.

The discovery of plutonium reorganized the periodic table and aided the discovery of new elements

International Nuclear Information System (INIS)

Clark, David L.

2009-01-01

The modern Periodic Table derives principally from the work of the great Russian scientist Dimitri Mendeleev, who in 1869 enunciated a 'periodic law' that the properties of the elements are a periodic function of their atomic weights, and arranged the 65 known elements in a 'periodic table'. Fundamentally, every column in the main body of the Periodic Table is a grouping of elements that display similar chemical and physical behavior. Similar properties are therefore exhibited by elements with widely different mass. Chemical periodicity is central to the study of chemistry, and no other generalization comes close to its ability to systematize and rationalize known chemical facts. With the development of atomic theory, and an understanding of the electronic structure of atoms, chemical periodicity and the periodic table now find their natural explanation in the electronic structure of atoms. Moving from left to right along any row, the elements are arranged sequentially according to nuclear charge (the atomic number). Electrons counter balance that nuclear charge, hence each successive element has one more electron in its configuration. The electron configuration, or distribution of electrons among atomic orbitals, may be determined by application of the Pauli principle (paired spin in the same orbital) and the aufbau principle (which outlines the order of filling of electrons into shells of orbitals - s, p, d, f, etc.) such that in a given atom, no two electrons may have all four quantum numbers identical. In 1939, only three elements were known to be heavier than actinium: thorium, protactinium, and uranium. All three exhibited variable oxidation states and a complex chemistry. Thorium, protactinium and uranium were assumed to be d-transition metals and were placed in the Periodic Table under hafnium, tantalum, and tungsten, respectively. By 1940, McMillan and Abelson bombarded uranium atoms with slow neutrons and successfully identified atoms of element 93, which

TheoSSA - Model WD Spectra on Demand: The Impact of Ne, Na, Mg, and Iron-group Elements on the Balmer Lines

Science.gov (United States)

Reindl, N.; Rauch, T.

2015-06-01

The registered German Astrophysical Virtual Observatory (GAVO) service TheoSSA provides easy access to synthetic stellar spectra. This GAVO database contains already ten thousands of these, which were calculated with different chemical compositions of the elements H to Ni. In addition to the database, it is possible to calculate individual spectra for hot, compact stars based on the Tübingen NLTE Model-Atmosphere Package (TMAP) via the TMAW service. The TMAW models were, in the pilot phase, restricted to the elements H, He, C, N, and O. Now, TMAW is extended to additionally consider opacities from Ne, Na, and Mg. Soon, TMAW will also be able to include the opacities from the so-called iron-group elements (Ca - Ni). We describe the improvements and show the impact of Ne, Na, Mg, and iron-group elements on the Balmer lines.

Coprecipitation experiment with Sm hydroxide using a multitracer produced by nuclear spallation reaction: A tool for chemical studies with superheavy elements

International Nuclear Information System (INIS)

Kasamatsu, Yoshitaka; Yokokita, Takuya; Toyomura, Keigo; Shigekawa, Yudai; Haba, Hiromitsu; Kanaya, Jumpei; Huang, Minghui; Ezaki, Yutaka; Yoshimura, Takashi; Morita, Kosuke; Shinohara, Atsushi

2016-01-01

To establish a new methodology for superheavy element chemistry, the coprecipitation behaviors of 34 elements with samarium hydroxide were investigated using multitracer produced by a spallation of Ta. The chemical reactions were rapidly equilibrated within 10 s for many elements. In addition, these elements exhibited individual coprecipitation behaviors, and the behaviors were qualitatively related to their hydroxide precipitation behaviors. It was demonstrated that the ammine and hydroxide complex formations of superheavy elements could be investigated using the established method. - Highlights: • We established a new methodology for superheavy element (SHE) chemistry. • Coprecipitation behaviors of 34 elements with Sm hydroxide could be simultaneously investigated by using multitracer. • The complex formations were investigated from the coprecipitation behaviors. • The established method will lead to the study on various precipitates of SHEs.

PETROS - Worldwide Databank of Major Element Chemical Analyses of Igneous Rocks

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — PETROS is a worldwide data bank of major element chemical analyses of igneous rocks compiled for research and teaching purposes by Dr. Felix Mutschler and Staff at...

Foreign Language Translation of Chemical Nomenclature by Computer

Science.gov (United States)

2009-01-01

Chemical compound names remain the primary method for conveying molecular structures between chemists and researchers. In research articles, patents, chemical catalogues, government legislation, and textbooks, the use of IUPAC and traditional compound names is universal, despite efforts to introduce more machine-friendly representations such as identifiers and line notations. Fortunately, advances in computing power now allow chemical names to be parsed and generated (read and written) with almost the same ease as conventional connection tables. A significant complication, however, is that although the vast majority of chemistry uses English nomenclature, a significant fraction is in other languages. This complicates the task of filing and analyzing chemical patents, purchasing from compound vendors, and text mining research articles or Web pages. We describe some issues with manipulating chemical names in various languages, including British, American, German, Japanese, Chinese, Spanish, Swedish, Polish, and Hungarian, and describe the current state-of-the-art in software tools to simplify the process. PMID:19239237

"Just as the Structural Formula Does": Names, Diagrams, and the Structure of Organic Chemistry at the 1892 Geneva Nomenclature Congress.

Science.gov (United States)

Hepler-Smith, Evan

2015-02-01

At the Geneva Nomenclature Congress of 1892, some of the foremost organic chemists of the late nineteenth century crafted a novel relationship between chemical substances, chemical diagrams, and chemical names that has shaped practices of chemical representation ever since. During the 1880s, the French chemist Charles Friedel organised the nomenclature reform effort that culminated in the Geneva Congress; in the disorderly nomenclature of German synthetic chemistry, Friedel saw an opportunity to advance French national interests and his own pedagogical goals. Friedel and a group of close colleagues reconceived nomenclature as a unified field, in which all chemical names ought to relate clearly to one another and to the structure of the compounds they represented. The German chemist Adolf von Baeyer went a step farther, arguing for names that precisely and uniquely corresponded to the structural formula of each compound, tailored for use in chemical dictionaries and handbooks. Baeyer's vision prevailed at the Geneva Congress, which consequently codified rules for rigorously mapping structural formulas into names, resulting in names that faithfully represented the features of these diagrams but not always the chemical behaviour of the compounds themselves. This approach ultimately limited both the number of chemical compounds that the Geneva rules were able to encompass and the breadth of their application. However, the relationship between diagram and name established at the Geneva Congress became the foundation not only of subsequent systems of chemical nomenclature but of methods of organising information that have supported the modern chemical sciences.

Determination of platinum-group elements in the geological standard reference materials by isotope dilution-ICPMS

Energy Technology Data Exchange (ETDEWEB)

Mingyue, Hu; Hongliao, He [National Research Center for Geoanalysis, Beijing (China)

2005-10-15

Platinum group elements (PGEs) includes platinum, palladium, iridium, osmium, rhodium and ruthenium. It has very high economic and scientific value in the field of geoscience and environmental science. But the analysis data referred by the different lab are very disperse because of the difficulty of the determination of PGEs. It makes very difficult to fix the value of the PGEs in the standard reference materials. In the article, the values of the PGEs in the standard reference materials of ocean sediment are determined by isotope dilution technique and dependable values of these elements are provided. (authors)

Determination of platinum-group elements in the geological standard reference materials by isotope dilution-ICPMS

International Nuclear Information System (INIS)

Hu Mingyue; He Hongliao

2005-01-01

Platinum group elements (PGEs) includes platinum, palladium, iridium, osmium, rhodium and ruthenium. It has very high economic and scientific value in the field of geoscience and environmental science. But the analysis data referred by the different lab are very disperse because of the difficulty of the determination of PGEs. It makes very difficult to fix the value of the PGEs in the standard reference materials. In the article, the values of the PGEs in the standard reference materials of ocean sediment are determined by isotope dilution technique and dependable values of these elements are provided. (authors)

Newer trace elements measured by RNNA and AAS

International Nuclear Information System (INIS)

Gharib, A.G.

2004-01-01

Very recently, special attention has been made on a few more trace elements in foodstuff as newer essential for animal and human health in certain ranges of concentration or intakes. These traces are namely: Aluminium, Nickel, Vanadium and Tin. A1 and Ni have been measured by Atomic Absorption Spectroscopy and two latter ones measured by Radiochemical Neutron Activation Analysis in some references laboratories. Here also scandium was analyzed by Instrumental Neutron Activation Analysis as well. These measurements were made for the most of Iranian diets and other participant countries' diets in frame of coordinated research project led by International Atomic Energy Agency period of 1986-1994, but practically it took more years. Here in this work the daily dietary intakes of aforesaid trace elements are given and discussed while the results of other 20 more nutritionally important trace elements were appeared somewhere else

Platinum group elements geochemistry of ultramafic and associated ...

Indian Academy of Sciences (India)

group element (PGE) and associated gold mineralization in these ultramafic rocks. A mineral ... Paleoproterozoic age, mostly emplaced into the .... tified reference materials (CRM) from the US Geo- ..... Classification diagram (Barnes et al.

Contamination of Kallar Kahar Lake by Inorganic Elements and ...

African Journals Online (AJOL)

The present study was conducted to find out the contamination of Kallar Kahar Lake by inorganic elements and heavy metals and the temporal variation of these chemicals in the lake water. Water samples were collected on monthly basis during December 2001 to November 2002. Concentration of 10 inorganic elements ...

The uses of synchrotron radiation sources for elemental and chemical microanalysis

Science.gov (United States)

Chen, J.R.; Chao, E.C.T.; Minkin, J.A.; Back, J.M.; Jones, K.W.; Rivers, M.L.; Sutton, S.R.

1990-01-01

Synchrotron radiation sources offer important features for the analysis of a material. Among these features is the ability to determine both the elemental composition of the material and the chemical state of its elements. For microscopic analysis synchrotron X-ray fluorescence (SXRF) microprobes now offer spatial resolutions of 10 ??m with minimum detection limits in the 1-10 ppm range depending on the nature of the sample and the synchrotron source used. This paper describes the properties of synchrotron radiation and their importance for elemental analysis, existing synchrotron facilities and those under construction that are optimum for SXRF microanalysis, and a number of applications including the high energy excitation of the K lines of heavy elements, microtomography, and XANES and EXAFS spectroscopies. ?? 1990.

Toxic industrial chemicals and chemical weapons: exposure, identification, and management by syndrome.

Science.gov (United States)

Tomassoni, Anthony J; French, Robert N E; Walter, Frank G

2015-02-01

Toxidromes aid emergency care providers in the context of the patient presenting with suspected poisoning, unexplained altered mental status, unknown hazardous materials or chemical weapons exposure, or the unknown overdose. The ability to capture an adequate chemical exposure history and to recognize toxidromes may reduce dependence on laboratory tests, speed time to delivery of specific antidote therapy, and improve selection of supportive care practices tailored to the etiologic agent. This article highlights elements of the exposure history and presents selected toxidromes that may be caused by toxic industrial chemicals and chemical weapons. Specific antidotes for toxidromes and points regarding their use, and special supportive measures, are presented. Copyright © 2015 Elsevier Inc. All rights reserved.

Molecular clusters of the main group elements

CERN Document Server

Driess, Matthias

2008-01-01

""To summarize, Molecular Clusters of the Main Group Elements is certainly not a popular science book, nor is it a textbook; it is a very good, up-to-date collection of articles for the specialist. Als Fazit bleibt: Molecular Clusters of the Main Group Elements ist sicher kein populissenschaftliches Werk, auch kein Lehrbuch, aber eine gelungene, hoch aktuelle Zusammenstellung fen interessierten Fachmann."" -Michael Ruck, TU Dresden, Angewandte Chemie, 2004 - 116/36 + International Edition 2004 - 43/36

Measurements of radon and chemical elements: Popocatepetl volcano; Mediciones de radon y elementos quimicos: Volcan Popocatepetl

Energy Technology Data Exchange (ETDEWEB)

Pena, P.; Segovia, N.; Lopez, B.; Reyes, A.V. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Armienta, M.A.; Valdes, C.; Mena, M. [IGFUNAM, Ciudad Universitaria, 04510 Mexico D.F. (Mexico); Seidel, J.L.; Monnin, M. [UMR 5569 CNRS Hydrosciences, Montpellier (France)

2002-07-01

The Popocatepetl volcano is a higher risk volcano located at 60 Km from Mexico City. Radon measurements on soil in two fixed seasons located in the north slope of volcano were carried out. Moreover the radon content, major chemical elements and tracks in water samples of three springs was studied. The radon of soil was determined with solid detectors of nuclear tracks (DSTN). The radon in subterranean water was evaluated through the liquid scintillation method and it was corroborated with an Alpha Guard equipment. The major chemical elements were determined with conventional chemical methods and the track elements were measured using an Icp-Ms equipment. The radon on soil levels were lower, indicating a moderate diffusion of the gas across the slope of the volcano. The radon in subterranean water shown few changes in relation with the active scene of the volcano. The major chemical elements and tracks showed a stable behavior during the sampling period. (Author)

Origin and Evolution of the Elements

Science.gov (United States)

McWilliam, Andrew; Rauch, Michael

2004-09-01

Introduction; List of participants; 1. Mount Wilson Observatory contributions to the study of cosmic abundances of the chemical elements George W. Preston; 2. Synthesis of the elements in stars: B2FH and beyond E. Margaret Burbidge; 3. Stellar nucleosynthesis: a status report 2003 David Arnett; 4. Advances in r-process nucleosynthesis John J. Cowan and Christopher Sneden; 5. Element yields of intermediate-mass stars Richard B. C. Henry; 6. The impact of rotation on chemical abundances in red giant branch stars Corinne Charbonnel; 7. s-processing in AGB stars and the composition of carbon stars Maurizio Busso, Oscar Straniero, Roberto Gallino, and Carlos Abia; 8. Models of chemical evolution Francesca Matteucci; 9. Model atmospheres and stellar abundance analysis Bengt Gustafsson; 10. The light elements: lithium, beryllium, and boron Ann Merchant Boesgaard; 11. Extremely metal-poor stars John E. Norris; 12. Thin and thick galactic disks Poul E. Nissen; 13. Globular clusters and halo field stars Christopher Sneden, Inese I. Ivans and Jon P. Fulbright; 14. Chemical evolution in ω Centauri Verne V. Smith; 15. Chemical composition of the Magellanic Clouds, from young to old stars Vanessa Hill; 16. Detailed composition of stars in dwarf spheroidal galaxies Matthew D. Shetrone; 17. The evolutionary history of Local Group irregular galaxies Eva K. Grebel; 18. Chemical evolution of the old stellar populations of M31 R. Michael Rich; 19. Stellar winds of hot massive stars nearby and beyond the Local Group Fabio Bresolin and Rolf P. Kudritzki; 20. Presolar stardust grains Donald D. Clayton and Larry R. Nittler; 21. Interstellar dust B. T. Draine; 22. Interstellar atomic abundances Edward B. Jenkins; 23. Molecules in the interstellar medium Tommy Wiklind; 24. Metal ejection by galactic winds Crystal L. Martin; 25. Abundances from the integrated light of globular clusters and galaxies Scott C. Trager; 26. Abundances in spiral and irregular galaxies Donald R. Garnett; 27

Modifications of chemical functional groups of Pandanus amaryllifolius Roxb and its effect towards biosorption of heavy metals

Energy Technology Data Exchange (ETDEWEB)

Abdullah, Mohd Zamri, E-mail: zamriab@petronas.com.my; Ismail, Siti Salwa [Chemical Engineering Department, Universiti Teknologi PETRONAS, 31750 Bandar Seri Iskandar, Perak (Malaysia)

2015-07-22

The utilization of non-living biomass as an alternative biosorbent for heavy metal removal has gain a tremendous consideration through the years. Pandanus amaryllifolius Roxb or pandan leaves, which is widely used as food additives in the South East Asia region, has been selected for its viability in the said effort due to the presence of chemical functional groups on its cellular network that enables the sorption to occur. In order to elucidate the possible mechanisms participated during the heavy metal removal process, the biosorbent undergone a series of modification techniques to alter the chemical functional groups present on its constituent. From the outcome of the chemically-modified biosorbent being subjected to the contact with metal cations, nitrogen- and oxygen-containing groups present on the biosorbent are believed to be responsible for the metal uptake to occur through complexation mechanism. Modifying amine groups causes 14% reduction of Cu(II) uptake, whereas removing protein element increases the uptake to 26% as compared to the unmodified biosorbent. Also, scanning electron micrographs further suggested that the adsorption mechanism could perform in parallel, as attributed to the evidence of porous structure throughout the biosorbent fibrous nature.

Modifications of chemical functional groups of Pandanus amaryllifolius Roxb and its effect towards biosorption of heavy metals

International Nuclear Information System (INIS)

Abdullah, Mohd Zamri; Ismail, Siti Salwa

2015-01-01

The utilization of non-living biomass as an alternative biosorbent for heavy metal removal has gain a tremendous consideration through the years. Pandanus amaryllifolius Roxb or pandan leaves, which is widely used as food additives in the South East Asia region, has been selected for its viability in the said effort due to the presence of chemical functional groups on its cellular network that enables the sorption to occur. In order to elucidate the possible mechanisms participated during the heavy metal removal process, the biosorbent undergone a series of modification techniques to alter the chemical functional groups present on its constituent. From the outcome of the chemically-modified biosorbent being subjected to the contact with metal cations, nitrogen- and oxygen-containing groups present on the biosorbent are believed to be responsible for the metal uptake to occur through complexation mechanism. Modifying amine groups causes 14% reduction of Cu(II) uptake, whereas removing protein element increases the uptake to 26% as compared to the unmodified biosorbent. Also, scanning electron micrographs further suggested that the adsorption mechanism could perform in parallel, as attributed to the evidence of porous structure throughout the biosorbent fibrous nature

"gnparser": a powerful parser for scientific names based on Parsing Expression Grammar.

Science.gov (United States)

Mozzherin, Dmitry Y; Myltsev, Alexander A; Patterson, David J

2017-05-26

Scientific names in biology act as universal links. They allow us to cross-reference information about organisms globally. However variations in spelling of scientific names greatly diminish their ability to interconnect data. Such variations may include abbreviations, annotations, misspellings, etc. Authorship is a part of a scientific name and may also differ significantly. To match all possible variations of a name we need to divide them into their elements and classify each element according to its role. We refer to this as 'parsing' the name. Parsing categorizes name's elements into those that are stable and those that are prone to change. Names are matched first by combining them according to their stable elements. Matches are then refined by examining their varying elements. This two stage process dramatically improves the number and quality of matches. It is especially useful for the automatic data exchange within the context of "Big Data" in biology. We introduce Global Names Parser (gnparser). It is a Java tool written in Scala language (a language for Java Virtual Machine) to parse scientific names. It is based on a Parsing Expression Grammar. The parser can be applied to scientific names of any complexity. It assigns a semantic meaning (such as genus name, species epithet, rank, year of publication, authorship, annotations, etc.) to all elements of a name. It is able to work with nested structures as in the names of hybrids. gnparser performs with ≈99% accuracy and processes 30 million name-strings/hour per CPU thread. The gnparser library is compatible with Scala, Java, R, Jython, and JRuby. The parser can be used as a command line application, as a socket server, a web-app or as a RESTful HTTP-service. It is released under an Open source MIT license. Global Names Parser (gnparser) is a fast, high precision tool for biodiversity informaticians and biologists working with large numbers of scientific names. It can replace expensive and error

Effects of chemical elements in the trophic levels of natural salt marshes.

Science.gov (United States)

Kamiński, Piotr; Barczak, Tadeusz; Bennewicz, Janina; Jerzak, Leszek; Bogdzińska, Maria; Aleksandrowicz, Oleg; Koim-Puchowska, Beata; Szady-Grad, Małgorzata; Klawe, Jacek J; Woźniak, Alina

2016-06-01

The relationships between the bioaccumulation of Na, K, Ca, Mg, Fe, Zn, Cu, Mn, Co, Cd, and Pb, acidity (pH), salinity (Ec), and organic matter content within trophic levels (water-soil-plants-invertebrates) were studied in saline environments in Poland. Environments included sodium manufactures, wastes utilization areas, dumping grounds, and agriculture cultivation, where disturbed Ca, Mg, and Fe exist and the impact of Cd and Pb is high. We found Zn, Cu, Mn, Co, and Cd accumulation in the leaves of plants and in invertebrates. Our aim was to determine the selectivity exhibited by soil for nutrients and heavy metals and to estimate whether it is important in elucidating how these metals are available for plant/animal uptake in addition to their mobility and stability within soils. We examined four ecological plant groups: trees, shrubs, minor green plants, and water macrophytes. Among invertebrates, we sampled breastplates Malacostraca, small arachnids Arachnida, diplopods Diplopoda, small insects Insecta, and snails Gastropoda. A higher level of chemical elements was found in saline polluted areas (sodium manufactures and anthropogenic sites). Soil acidity and salinity determined the bioaccumulation of free radicals in the trophic levels measured. A pH decrease caused Zn and Cd to increase in sodium manufactures and an increase in Ca, Zn, Cu, Cd, and Pb in the anthropogenic sites. pH increase also caused Na, Mg, and Fe to increase in sodium manufactures and an increase in Na, Fe, Mn, and Co in the anthropogenic sites. There was a significant correlation between these chemical elements and Ec in soils. We found significant relationships between pH and Ec, which were positive in saline areas of sodium manufactures and negative in the anthropogenic and control sites. These dependencies testify that the measurement of the selectivity of cations and their fluctuation in soils provide essential information on the affinity and binding strength in these environments. The

A simple chemical method for the separation of phosphorus interfering the trace element determinations by neutron activation analysis in high doped silicon wafers

International Nuclear Information System (INIS)

Wagler, H.; Flachowsky, J.

1986-01-01

Neutron activation analysis is one of the most available method for the determination of trace elements, but in the case of P-doped silicon wafers the 32 P-activity interferes the gamma spectrometry. It is not possible to determine the trace elements without chemical manipulations. On the other hand, time consuming chemical separations should be avoided. Therefore, a simple and rapid P-separation method has to be developed, in which the following twelve trace elements should be taken into consideration: Ag, As, Au, Co, Cr, Cu, Fe, Mo, Na, Sb, W, and Zn. After acid oxidative dissolution of the activated sample, P is present as phosphate ion. The phosphate ion is removed by precipitation as BiPO 4 . (author)

The uses of synchrotron radiation sources for elemental and chemical microanalysis

International Nuclear Information System (INIS)

Chen, J.R.; Chao, E.C.T.; Minkin, J.A.; Back, J.M.; Jones, K.W.; Rivers, M.L.; Sutton, S.R.

1989-08-01

Synchrotron radiation sources offer important features for the analysis of a material. Among these features is the ability to determine both the elemental composition of the material and the chemical state of its elements. For microscopic analysis synchrotron x-ray fluorescence (SXRF) microprobes now offer spatial resolutions of 10μm with minimum detection limits in the 1--10 ppM range depending on the nature of the sample and the synchrotron source used. This paper describes the properties of synchrotron radiation and their importance for elemental analysis, existing synchrotron facilities and those under construction that are optimum for SXRF microanalysis, and a number of applications including the high energy excitation of the K lines of heavy elements, microtomography, and XANES and EXAFS spectroscopies. 45 refs., 8 figs., 1 tab

A study on chemical element determinations in human nails by neutron activation analysis

International Nuclear Information System (INIS)

Sanches, Thalita Pinheiro; Saiki, Mitiko

2013-01-01

Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10 12 n cm -2 s -1 at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO 3 solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in replicate. A

A study on chemical element determinations in human nails by neutron activation analysis

International Nuclear Information System (INIS)

Sanches, Thalita Pinheiro

2012-01-01

Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10 12 n cm -2 s -1 at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO 3 solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in replicate. A

A study on chemical element determinations in human nails by neutron activation analysis

Energy Technology Data Exchange (ETDEWEB)

Sanches, Thalita Pinheiro; Saiki, Mitiko, E-mail: thalitapsanches@usp.br, E-mail: mitiko@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2013-07-01

Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10{sup 12} n cm{sup -2} s{sup -1} at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO{sub 3} solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in

Chemical properties of some elements in a molten lithium chloride, potassium chloride eutectic (1962)

International Nuclear Information System (INIS)

Molina, R.

1961-12-01

The increasing use of molten media especially in chemical preparations and for certain technological applications, has made it more necessary to have a knowledge of the chemical properties of elements in these solvents. Structural studies on molten solutions show the existence of certain species such as ions and complexes known to exist in aqueous solutions. This fact, together with certain experiments on chemical reactions in molten media has led us to establish a comparison between these media and aqueous solutions. We wish to show that the same fundamental phenomena occur in these media as are found in the chemistry of aqueous solutions and that this makes it possible to predict certain reactions. We have taken as examples the chemical properties of vanadium, uranium and sulphur in a LiCl-KCl eutectic melted at 480 deg. C. The first problem is to identify the various degrees of oxidation of these elements existing in the solvent chosen. We have tried to resolve it by comparing the absorption spectra obtained in aqueous solution and in the molten eutectic. We consider the possibilities of this method in a chapter on absorption spectrophotometry in the LiCl-KCl eutectic. During the study of the chemical properties we stress the various methods of displacing the equilibria: complex formation, variation of the oxidation-reduction properties with complex formation. The complexes of the O 2- ion are considered in particular. The study of the exchange of this particle is facilitated by the use of a classification of some of its complexes which we call the pO 2- scale by analogy with the pH scale; the value pO 2- is defined by the relationship: pO 2- = log O 2- Similarly, the use of apparent potential diagrams pO 2- makes it possible to predict and to interpret reactions involving the simultaneous exchange of electrons and O 2- ions between the various degrees of oxidation of the same element. It is possible, by studying some reactions of this type between two elements

Fractionation of elements by particle size of ashes ejected from Copahue Volcano, Argentina.

Science.gov (United States)

Gómez, Dario; Smichowski, Patricia; Polla, Griselda; Ledesma, Ariel; Resnizky, Sara; Rosa, Susana

2002-12-01

The volcano Copahue, Neuquén province, Argentina has shown infrequent explosive eruptions since the 18th century. Recently, eruptive activity and seismicity were registered in the period July-October, 2000. As a consequence, ash clouds were dispersed by winds and affected Caviahue village located at about 9 km east of the volcano. Samples of deposited particles from this area were collected during this episode for their chemical analysis to determine elements of concern with respect to the health of the local population and its environment. Different techniques were used to evaluate the distribution of elements in four particle size ranges from 36 to 300 microm. X-ray powder diffraction (XRD) was selected to detect major components namely, minerals, silicate glass, fragments of rocks and sulfurs. Major and minor elements (Al, Ca, Cl, Fe, K, Mg, Mn, Na, S, Si and Ti), were detected by energy dispersive X ray analysis (EDAX). Trace element (As, Cd, Cr, Cu, Hg, Ni, Pb, Sb, U, V and Zn) content was quantified by inductively coupled plasma-mass spectrometry (ICP-MS). Nuclear activation analysis (NAA) was employed for the determination of Ce, Co, Cs, Eu, Hf, La, Lu, Rb, Sc, Sm, Ta and Yb. An enrichment was observed in the smallest size fraction of volcanic ashes for four elements (As, Cd, Cu and Sb) of particular interest from the environmental and human health point of view.

Airborne chemical elements in Spanish moss

Energy Technology Data Exchange (ETDEWEB)

Shacklette, H.T.; Connor, J.J.

1973-01-01

Spanish moss (Tillandsia usneoides L.), collected from its geographic range in Southern United States, was analyzed for 38 chemical elements in 123 samples. Analyses of Spanish moss samples collected at rural, residential, highway, and industrial locations reflected significant differences in concentrations of metals. Samples from industrial and highway locations are characterized as containing greater-than-average amounts of arsenic, cadmium, chromium, cobalt, copper, lead, nickel, and vanadium. The high levels of lead found in some samples from highway locations are especially noteworthy. Many samples from sites near the seashore contained greater-than-average amounts of sodium that is thought to have been derived from ocean spray. Samples from rural locations commonly contain low concentrations of the metal usually associated with industrial or urban activity but may contain large amounts of the elements that are ordinary constituents of soil dust. Four of six samples containing detectable amounts of tin were collected within 50 miles of the only tin smelter in the United States; this result suggests that elemental analyses of Spanish moss samples can provide an economical and rapid method of estimating the kind and relative degree of local atmospheric metal pollution.

Improving lead adsorption through chemical modification of wheat straw by lactic acid

Science.gov (United States)

Mu, Ruimin; Wang, Minxiang; Bu, Qingwei; Liu, Dong; Zhao, Yanli

2018-01-01

This work describes the creation of a new cellulosic material derived from wheat straw modified by lactic acid for adsorption of lead in aqueous solution, called 0.3LANS (the concentration of the lactic acid were 0.3mol/L). Batch experiments were conducted to study the effects of initial pH value, contact time, adsorbent dose, initial concentration and temperature. Fourier transform infrared (FTIR), Elemental analysis, BET surface area and Scanning electron micrographs (SEM) analysis were used to investigate the chemical modification. Adsorption isotherm models namely, Langmuir, Freundlich were used to analyse the equilibrium data, and the Langmuir isotherm model provided the best correlation, means that the adsorption was chemical monolayer adsorption and the adsorption capacity qm was increased with increasing temperature, and reached 51.49mg/g for 0.3LANS at 35°C, showing adsorption was exothermic.

Levels of platinum group elements and rare-earth elements in wild mushroom species growing in Poland.

Science.gov (United States)

Mleczek, Mirosław; Niedzielski, Przemysław; Kalač, Pavel; Siwulski, Marek; Rzymski, Piotr; Gąsecka, Monika

2016-01-01

Due to limited data-describing abilities of mushrooms to accumulate platinum group elements (PGEs) and rare-earth elements (REEs), the aim of this study was to determine, by inductively coupled plasma optical emission spectrometry followed by microwave-assisted sample digestion by nitric acid, the content of these elements in 20 mushroom species (10 above ground and 10 growing on wood), mostly edible, collected near a busy trunk road. The highest content of PGEs in above-ground mushroom species was observed in Lepista gilva and Suillus bovinus fruit bodies (0.38 ± 0.05 and 0.37 ± 0.03 mg kg(-1) DW, respectively), while in mushrooms growing on wood, the highest content was observed in Pleurotus ostreatus (0.35 ± 0.04 mg kg(-1) DW). The mean content of PGEs for both these groups was 0.23 ± 0.08 and 0.26 ± 0.07 mg kg(-1) DW, respectively. The highest content of REEs in Suillus luteus and Tricholoma equestra was 5.03 ± 0.50 and 2.18 ± 0.56 mg kg(-1) DW, respectively, but within mushrooms growing on wood in Ganoderma applanatum fruiting bodies it was 4.19 ± 0.78 mg kg(-1) DW. Mean contents of REEs were 1.39 ± 1.21 and 1.61 ± 0.97 mg kg(-1) DW in above-ground species and species growing on wood, respectively. Generally, the group of mushroom species growing on wood was capable of slightly higher accumulation of both REEs and PGEs. No limits have been established for both the groups until now.

Socioeconomic determinants of first names

NARCIS (Netherlands)

Bloothooft, G.; Onland, D.

2011-01-01

Modern naming practices in the Netherlands between 1982 and 2005 were studied on the basis of 1409 popular first names, divided into fourteen name groups determined by the common preferences of parents for the names involved. Socioeconomic variables such as family income, parents' level of

Phase distribution of ecologically controlled chemical elements in production of extraction phosphoric acid

International Nuclear Information System (INIS)

Kazak, V.G.; Agnelov, A.I.; Zajtsev, P.M.

1995-01-01

Content of 16 ecologically controlled chemical element (among them Cd, Sr, Th, U, V, Y) in solid and liquid phases of extraction phosphorus acid (EPA) production is determined. These elements are recommended to control by Scientific research institute of human ecology and environment to establish their extraction coefficients to phosphogypsum and EPA and optimal variant of production of ecologically sate phosphorus fertilizers. X-ray fluorescent, atomic-absorption and polarographic methods are used for analysis these elements

Solutions of group IV elements in liquid lithium

International Nuclear Information System (INIS)

Dadd, A.T.; Hubberstey, P.; Roberts, P.G.

1982-01-01

The solubilities of tin (0.00 = 22 Sn 5 . A simple thermochemical cycle is used to demonstrate that, whereas carbon dissolves endothermically in both liquid lithium and liquid sodium, the heavier Group IV elements dissolve exothermically. A similar cycle is used to derive solvation enthalpies (for the neutral gaseous species) for all Group IV elements in the two solvents. The trend in solvation enthalpy: C > Si > Ge > Sn > Pb is indicative of a diminishing affinity of solvent for solute and is attributed to the increasing metallic character of the solute as the Group is descended. (author)

Untangling the brand name from the branded entity

OpenAIRE

Round, Griff; Roper, Stuart

2015-01-01

Purpose\\ud – The purpose of this study is to investigate the value to consumers of the brand name element for established brands, given that the focus in the literature has been on new brands. To accomplish this, conceptual development was initially undertaken to illuminate the links between the brand name element and the brand entity and to provide a theoretical framework for looking at changes in value of the brand name element to consumers over time.\\ud \\ud Design/methodology/approach\\ud –...

The Open Cluster Chemical Abundances and Mapping (OCCAM) Survey: Optical Extension for Neutron Capture Elements

Science.gov (United States)

Melendez, Matthew; O'Connell, Julia; Frinchaboy, Peter M.; Donor, John; Cunha, Katia M. L.; Shetrone, Matthew D.; Majewski, Steven R.; Zasowski, Gail; Pinsonneault, Marc H.; Roman-Lopes, Alexandre; Stassun, Keivan G.; APOGEE Team

2017-01-01

The Open Cluster Chemical Abundance & Mapping (OCCAM) survey is a systematic survey of Galactic open clusters using data primarily from the SDSS-III/APOGEE-1 survey. However, neutron capture elements are very limited in the IR region covered by APOGEE. In an effort to fully study detailed Galactic chemical evolution, we are conducting a high resolution (R~60,000) spectroscopic abundance analysis of neutron capture elements for OCCAM clusters in the optical regime to complement the APOGEE results. As part of this effort, we present Ba II, La II, Ce II and Eu II results for a few open clusters without previous abundance measurements using data obtained at McDonald Observatory with the 2.1m Otto Struve telescope and Sandiford Echelle Spectrograph.This work is supported by an NSF AAG grant AST-1311835.

Mechanism and degree of chemical elements effect on atmosphere corrosion resistance of steels

International Nuclear Information System (INIS)

Vu Din' Vuj

1991-01-01

It follows from the proposed regression equations that falourable effect of chemical elements on steel resistance to atmospheric corrosion is determined by their ability to increase interatom bond stability in iron crystal lattice and form corrosion products with high protection properties. Element positive influence on steel corrosion resistance decreases in the following order: S, P, Si, Mn, Cu, Cr, Ni, C in semiurban tropical atmosphere and S, Mn, Sr, Cu, Ni, Cr in coastal atmosphere. In the latter case C increases corrosion in a greater degree as compared to P. Small ammounts of Mo decrease steel resistance in semiurban atmosphere and almost do not influence it in the coastal one. Possible mechanisms of individual element influence on steel corrosion resistance are considered

Elements of theory of abelian groups

International Nuclear Information System (INIS)

Lebedenko, V.M.

1977-01-01

Some methods and results of studies on the abelian group theory being an important branch of modern algebra are presented. Some examples of the application of the abelian groups in physics are given. A primary information on commutative groups is presented. The concepts of a group, a subgroup, homomorphism, an order of element are given; those of torsion, torsion-free and mixed groups are considered, as well as the concepts of direct and full direct sums. The concepts of a free group and defining relations, of linear dependence and a rank are given. The main classes of abelian groups and subgroup types are described. Some classical results on the abelian group theory are presented, its modern state is described, the links with other regions of algebra are presented

Rare earths: critical elements for various applications and challenges in their separation

International Nuclear Information System (INIS)

Singh, D.K.; Chakravartty, J.K.

2015-01-01

High purity rare earths oxides, metal and alloys find wide applications in high tech area such as nuclear energy, permanent magnets, materials for storing hydrogen, phosphors, laser, etc. Rare earths consists a group of 15 elements from La to Lu in the periodic table and it also includes Sc and Y. Due to similar chemical nature owing to common oxidation state of +3, rare earths are very difficult to separate from each other. They have very low separation factors with acidic extractants like D2EHPA and EHEHPA and hence require large number of stages in various cascade of extraction process. Monazite (a source of rare earths, thorium and uranium) is processed at IREL to separate rare earths from thorium and uranium. The rare earths are fractionated into three groups namely light rare earths (LRE), middle rare earths (MRE) and heavy rare earths (HRE) by solvent extraction method employing EHEHPA as extractant

Periodic table of elements

International Nuclear Information System (INIS)

Fluck, E.; Heumann, K.G.

1985-01-01

Following a recommendation by the International Union for Pure and Applied Chemistry (IUPAC), the groups of the periodic table shall be numbered from 1 to 18, instead of I to VIII as before. The recommendations has been approved of by the Committee on Nomenclature of the American Chemical Society. The new system abandons the distinction between main groups (a) and auxiliary groups (b), which in the past frequently has been the reason for misunderstandings between European and American chemists, due to different handling. The publishing house VCH Verlagsgesellschaft recently produced a new periodic table that shows the old and the new numbering system together at a glance, so that chemists will have time to get familiar with the new system. In addition the new periodic table represents an extensive data compilation arranged by elements. The front page lists the chemical properties of elements, the back page their physical properties. (orig./EF) [de

Dynamics of chemical elements in the fermentation process of ethanol production

International Nuclear Information System (INIS)

Nepomuceno, N.; Fernandes, E.A.N.; Bacchi, M.A.

1997-01-01

Brazil has become the largest producer of biomass ethanol derived from sugar cane. The industrial production is based on the fermentation of sugar cane juice by yeast, inside of large volume vats, in a fed-batch process that recycles yeast cells. To study the dynamics of chemical elements in each operating cycle, five stages of the fermentation process were considered: must, yeast suspension, wine, non-yeast wine and yeast cream. For this, a mass balance of the terrigenous elements, Ce, Co, Cs, Eu, Fe, Hf, La, Na, Sc, Sm, and Th, and the sugar cane plant elements, Br, K, Rb, and Zn, were established in fermentation vats of an industrial scale unit, with sampling undertaken during different climatic conditions (dry and rainy periods). A similar distribution of the sugar cane characteristics elements was found for the stages analysed, while for the terrigenous elements a trend of accumulation in the yeast cream was observed. Preferential absorption of Br, K, Rb, and Zn by yeast cells was indicated by the smaller concentrations observed in yeast suspension than in yeast cream. (author)

Matching Element Symbols with State Abbreviations: A Fun Activity for Browsing the Periodic Table of Chemical Elements

Science.gov (United States)

Woelk, Klaus

2009-01-01

A classroom activity is presented in which students are challenged to find matches between the United States two-letter postal abbreviations for states and chemical element symbols. The activity aims to lessen negative apprehensions students might have when the periodic table of the elements with its more than 100 combinations of letters is first…

Organometallic compounds of the 2-6 group elements of periodic system as perspective substances for microelectrnics

International Nuclear Information System (INIS)

Fedorov, V.A.

1986-01-01

Results of investigating methods of preparation and analysis of organometallic compounds (OMC) of the 2B-6B group elements, behaviour of microimpurities in the process of their complete purification, physical-chemical properties for developing rational flowsheets of OMC purification are presented. Results of microimpurities quantitative transition from OMC to gallium arsenide epitaxial layers are presented. Prospects for OMC application in microelectronics are discussed

Elemental investigation on Spanish dinosaur bones by x-ray fluorescence

International Nuclear Information System (INIS)

Brunetti, Antonio; Golosio, Bruno; Stegel, Giovanni; Piga, Giampaolo; Lasio, Barbara; Oliva, Piernicola; Enzo, Stefano

2013-01-01

In this paper we examine the chemical composition results obtained on a collection of 18 dinosaur fossil bones from Spain studied using a portable x-ray fluorescence spectrometer together with a reverse Monte Carlo numerical technique of data analysis. This approach is applied to the hypothesis of arbitrarily rough surfaces in order to account for the influence of the surface state of specimens on the chemical content evaluation. It is confirmed that the chemical content of elements is essential for understanding the changes brought about by diagenetic and taphonomic processes. However, for precise knowledge of what changes fossil bones have undergone after animal life and burial, it is necessary to use a multi-technique approach making use of other instruments like x-ray diffraction in order to describe accurately the transformations undergone by the mineralogical and bioinorganic phases and the properties of specific molecular groups. (paper)

Risk from environmental chemicals

Energy Technology Data Exchange (ETDEWEB)

Somers, E [Environmental Health Directorate, Health Protection Branch, Health and Welfare Canada, Ontario

1982-01-01

The elements of risk assessment, namely risk identification, risk estimation, risk evaluation and risk management, are described with respect to the control of environmental chemicals. The methodology of risk estimation is outlined and examples given of its application to regulatory decision-making for a number of chemicals in Canada. Finally, the extent and limitations of the process of risk evaluation are considered together with the need to recognize the importance of the public's perception of the level of risk.

Method and System for Name Resolution Across Heterogeneous Architectures

Science.gov (United States)

Sevilla, Spencer (Inventor); Mahadevan, Priya (Inventor); Garcia-Luna-Aceves, Jose J. (Inventor)

2018-01-01

One embodiment of the present invention provides a system for resolving a name request in a network comprising a plurality of groups that use different name-resolution schemes. During operation, the system receives, at a first group, the name request; identifies a parent group of the first group, which is a member of the parent group; and in response to failing to resolve the name request within the first group, forwards the name request to the identified parent group.

Heavy elements abundances in metal-poor stars

International Nuclear Information System (INIS)

Magain, P.; Jehin, E.; Neuforge, C.; Noels, A.

1998-01-01

A sample of 21 metal-poor stars have been analysed on the basis of high resolution and high signal-to-noise spectra. Correlations between relative abundances of 16 elements have been studied, with a special emphasis on the neutron-capture ones. This analysis reveals the existence of two sub-populations of field halo stars, namely Pop IIa and Pop IIb. They differ by the behaviour of the s-process elements versus the α and r-process elements. We suggest a scenario of formation of these stars, which closely relates the field halo stars to the evolution of globular clusters. The two sub-populations would have evaporated the clusters during two different stages of their chemical evolution

Chemical elements in common vegetable components of Portuguese diets, determined by k 0-INAA

International Nuclear Information System (INIS)

Pacheco, A.M.G.; Freitas, M.C.; Ventura, M.G.; Dionisio, I.; Ermakova, E.

2006-01-01

Vegetables play an important role in national diets, as a side dish to many a main-course fare the whole year round, and, especially in what concerns raw lettuce and tomato, with a higher seasonal rate of consumption during summer months, as associated to the traditional charcoal-grilled sardines. In March 2004, lettuces, tomatoes, carrots and cabbages of Portuguese origin (except for the carrots from one site) were purchased from large commercial areas or central markets of two central and southern regional hubs, respectively Coimbra and Evora. Even if from different growers, all vegetables had come from horticultural plots in the same general area of western Portugal, north of Lisboa. For lettuce plants, the inner leaves were separated from the external ones and processed as different samples for further analysis. In this work, the reactor and detector parameters were re-evaluated for the new IAEA k 0 -INAA software. Quality assessment was obtained through analysis of IAEA-359 (cabbage material) and BCR-679 (Bowen's kale). Traces of hazardous elements-namely, antimony, arsenic and bromine-could be found throughout, and, for lettuce samples, the overall results indicate that outer leaves feature higher concentrations than inner ones. Interestingly enough, vegetables from Coimbra and Evora appeared to differ from each other in their elemental levels, even if originally grown at relatively close range. Concentrations of trace elements are compared to available data from other countries' cultivars

The probability that a pair of group elements is autoconjugate

Indian Academy of Sciences (India)

[1] Alghamdi A M and Russo F G, A generalization of the probability that the commutator of two group elements is equal to a given element, Bull. Iranian Math. Soc. 38 (2012). 973–986. [2] Blackburn S R, Britnell J R and Wildon M, The probability that a pair of elements of a finite group are conjugate, J. London Math. Soc.

Induction by Coinduction and Control Operators in Call-by-Name

Directory of Open Access Journals (Sweden)

Yoshihiko Kakutani

2013-09-01

Full Text Available This paper studies emulation of induction by coinduction in a call-by-name language with control operators. Since it is known that call-by-name programming languages with control operators cannot have general initial algebras, interaction of induction and control operators is often restricted to effect-free functions. We show that some class of such restricted inductive types can be derived from full coinductive types by the power of control operators. As a typical example of our results, the type of natural numbers is represented by the type of streams. The underlying idea is a counterpart of the fact that some coinductive types can be expressed by inductive types in call-by-name pure language without side-effects.

Model Experiments on Chemical Properties of Superheavy Elements in Aqueous Solutions

CERN Document Server

Szeglowski, Z

2003-01-01

This paper presents a brief review of model experiments on investigation of chemical properties of transactinide elements, ranging from 104 to 116. The possibilities of isolation of the nuclei of these elements from nuclear reaction products, using the ion-exchange method, are also considered.

Chemical elements in Leucaena leucocephala leaves of riparian zones of the municipality of Piracicaba, São Paulo, Brazil

International Nuclear Information System (INIS)

França, Elvis J. de; Fernandes, Elisabete A.N.; Lira, Marcelo G.; Ferreira, Fabiano S.; Cavalca, Isabel P.O.; Rodrigues, Vanessa S.; Camilli, Leandro

2017-01-01

The species Leucaena leucocephala can be found in several riparian ecosystems, acting as one of the main invasive and harmful species for the forest restoration of the permanent preservation areas. It has also been studied for the phytoremediation of some chemical elements, due to their potential accumulation of chemical substances. Therefore, the present study aimed to evaluate the accumulation of chemical elements in leaves of Leucaena leucocephala trees by Instrumental Neutronic Activation Analysis - INAA. Samples of leaves were collected in eight samples from riverside areas of the Piracicaba Municipality, São Paulo, Brazil, during the dry and rainy season. After collection, washing with water and drying in a forced circulation oven, the samples were comminuted and encapsulated in polyethylene capsules and subjected to a thermal neutron flux of 10 13 cm -2 s -1 for 8 hours in the Nuclear Research Reactor IEA-R1 of IPEN / CNEN. Thermal neutron flux monitoring was performed by Ni-Cr alloy fragments with known concentrations of the chemical monitors elements. After measurements of radioactivity induced by HPGe detectors, the concentrations of the chemical elements were calculated by the k0 method using the Quantu computer program. Certified reference materials were also analyzed for quality assurance of the analytical procedure. The results indicated high concentrations of La and lanthanoids (Ce, Eu, Sm, Tb and Yb) in leaves of L. leucocephala in both periods analyzed. It was possible to observe a decrease in the concentrations of the chemical elements in the rainy season, probably associated to the washing of the geological material deposited on the leaves of the trees by the rains, except for K, Mo, Rb, Sb and Zn, whose values remained or increased in the leaves collected during the rainy season. Considering the constant leaf production, L. leucocephala can greatly affect the cycling of chemical elements due to its accumulation capacity demonstrated by this

Determination of minor-and trace elements in magnesite samples, by activation analysis

International Nuclear Information System (INIS)

Sepulveda Munita, C.J.A.

1979-01-01

A method employing activation analysis with thermal neutron was developed for the determination of minor and trace elements in magnesite samples from the states of Ceara and Bahia (Brazil). Ten samples were analyzed. A qualitative analysis of the samples indicated the presence of Mn, Fe, Sc, Ca, Cu, Co and some of the lanthanides. The experimental part includes a non-destructive analysis of manganese and analysis with chemical separation of the other elements, individually or in groups, after sample dissolution, The dissolutions were made with concentrated HCl and the further separations were carried out in 8 N HCl medium. Iron was separated by means of an extraction of HFeCl 4 with isopropyl ether. Scandium and calcium were determined by retention of scandium with di-(2-ehylhexyl) phosphoric acid (HDEHP). The activities of 46 Sc and 47 Sc (a 47 Ca descendant) were employed for the analysis of scandium and calcium in the sample. In the effluent of the kieselguhr column copper and cobalt were determined, after retention in an anionic resin of the CuCl - 3 and CoCl - 3 complexes. Finally, in the effluent of the resin, the lanthanide group was separated by oxalate precipitation. In the gamma-ray spectrum of this precipitate the elements europium, cerium, samarium and lanthanum were determined. A detailed study of the possible interferences in the neutron activation analysis of the elements analysed was also made. The precision and accuracy of the results obtained and the sensitivity of the method are discussed. (Author) [pt

Simultaneous topographic and elemental chemical and magnetic contrast in scanning tunneling microscopy

Science.gov (United States)

Rose, Volker; Preissner, Curt A; Hla, Saw-Wai; Wang, Kangkang; Rosenmann, Daniel

2014-09-30

A method and system for performing simultaneous topographic and elemental chemical and magnetic contrast analysis in a scanning, tunneling microscope. The method and system also includes nanofabricated coaxial multilayer tips with a nanoscale conducting apex and a programmable in-situ nanomanipulator to fabricate these tips and also to rotate tips controllably.

MARKED PERSONAL NAMES: AN ANTROPONIMIC STUDY OF BALINESE STUDENTS’ NAMES IN DENPASAR

Directory of Open Access Journals (Sweden)

Ni Made Iwan Indrawan

2015-07-01

Full Text Available The research aims to account for the Marked Balinese Students’ Personal Names. Four research problems are studied, namely (1 the criteria used to distinguish the marked names (NDMBmk and the unmarked ones (NDMTBmk, (2 the functions of the markedness, (3 the factors that influence it, and (4 the ideologies that operate behind it. The markedness of personal names reflect a relation between the arbitrariness in language uses and the extralinguistic factors influencing it. In the context of Balinese, the tradition, legal practices, and the globalisation may affect the arbitrariness. In order to determine NDMBmk, criteria of markedness was constructed. According to the criteria, structurally, NDMBmk consist of at least five elements, as Anak Agung Arim Kasunu Arya Penarungan. Behaviorally, they may consist of names not derived from Balinese and/or Sanskrit, such as Giovani on I Gede Adeyaka Giovani, adopt a foreign spelling system as Chrisna on Ni Putu Chrisna Wulandari, or use no markers of Balinese ethnics or caste as Yunisari Wira Putri. Out of 698 sampled names, NDMBmk are found 54. Besides denoting, the marked elements also function to distinguish personal identities, to shape the existence of the name holder, to connote particular perception, and to reflect the changing era. The factors influencing the markedness are the need to express something new, a wish to acculturate, to raise status or keep a distance socially, and to demonstrate a linguistic expertise, or when seeing from the concept of imagery, the factors are the imagery on something new and on social status or distancing. The ideologies behind the phenomenon are globalist, nationalist, and the casteless-Balinese.

MARKED PERSONAL NAMES: AN ANTROPONIMIC STUDY OF BALINESE STUDENTS’ NAMES IN DENPASAR

Directory of Open Access Journals (Sweden)

Ni Made Iwan Indrawan

2012-07-01

Full Text Available The research aims to account for the Marked Balinese Students’ Personal Names. Four research problems are studied, namely (1 the criteria used to distinguish the marked names (NDMBmk and the unmarked ones (NDMTBmk, (2 the functions of the markedness, (3 the factors that influence it, and (4 the ideologies that operate behind it. The markedness of personal names reflect a relation between the arbitrariness in language uses and the extralinguistic factors influencing it. In the context of Balinese, the tradition, legal practices, and the globalisation may affect the arbitrariness. In order to determine NDMBmk, criteria of markedness was constructed. According to the criteria, structurally, NDMBmk consist of at least five elements, as Anak Agung Arim Kasunu Arya Penarungan. Behaviorally, they may consist of names not derived from Balinese and/or Sanskrit, such as Giovani on I Gede Adeyaka Giovani, adopt a foreign spelling system as Chrisna on Ni Putu Chrisna Wulandari, or use no markers of Balinese ethnics or caste as Yunisari Wira Putri. Out of 698 sampled names, NDMBmk are found 54. Besides denoting, the marked elements also function to distinguish personal identities, to shape the existence of the name holder, to connote particular perception, and to reflect the changing era. The factors influencing the markedness are the need to express something new, a wish to acculturate, to raise status or keep a distance socially, and to demonstrate a linguistic expertise, or when seeing from the concept of imagery, the factors are the imagery on something new and on social status or distancing. The ideologies behind the phenomenon are globalist, nationalist, and the casteless-Balinese.

Parallel and Serial Grouping of Image Elements in Visual Perception

Science.gov (United States)

Houtkamp, Roos; Roelfsema, Pieter R.

2010-01-01

The visual system groups image elements that belong to an object and segregates them from other objects and the background. Important cues for this grouping process are the Gestalt criteria, and most theories propose that these are applied in parallel across the visual scene. Here, we find that Gestalt grouping can indeed occur in parallel in some…

Distribution of chemical elements in attic dust as reflection of their geogenic and anthropogenic sources in the vicinity of the copper mine and flotation plant.

Science.gov (United States)

Balabanova, Biljana; Stafilov, Trajče; Sajn, Robert; Bačeva, Katerina

2011-08-01

The main aim of this article was to assess the atmospheric pollution with heavy metals due to copper mining Bučim near Radoviš, the Republic of Macedonia. The open pit and mine waste and flotation tailings are continually exposed to open air, which leads to winds carrying the fine particles into the atmosphere. Samples of attic dust were examined as historical archives of mine emissions, with the aim of elucidating the pathways of pollution. Dust was collected from the attics of 29 houses, built between 1920 and 1970. Nineteen elements (Ag, Al, As, Ba, Ca, Cd, Co, Cr, Cu, Li, Fe, K, Mg, Mn, Na, Ni, Pb, Sr, and Zn) were analyzed by atomic emission spectrometry with inductively coupled plasma. The obtained values of the investigated elements in attic dust samples were statistically processed using nonparametric and parametric analysis. Factor analysis revealed three factors governing the source of individual chemical elements. Two of them grouping Ca, Li, Mg, Mn, and Sr (Factor 1) and Co, Cr, and Ni (Factor 2) can be characterized as geogenic. The third factor grouping As, Cu, and Pb is anthropogenic and mirrors dust fallout from mining operation and from flotation tailings. Maps of areal deposition were prepared for this group of elements, from which correlation of these anthropogenic born elements was confirmed.

The probability that a pair of group elements is autoconjugate

Indian Academy of Sciences (India)

Let and ℎ be arbitrary elements of a given finite group . Then and ℎ are said to be autoconjugate if there exists some automorphism of such that ℎ = . In this article, we construct some sharp bounds for the probability that two random elements of are autoconjugate, denoted by P a ( G ) . It is also shown that P ...

Quantum Chemical: New name and focus for National Distillers

Energy Technology Data Exchange (ETDEWEB)

Reisch, M.S.

1988-03-14

This article explains why the National Distillers and Chemical Corporation has narrowed its focus on petrochemicals and energy. At one time the company had diversified into wine and spirits, insurance, metals, chemicals and energy. However, the company decided to reexamine where its commitments should be. It decided to stick with chemicals and energy because it could be a leader in these fields and not in its other interests. The article explains how the new company, Quantum Chemical, is doing and where it is headed in the future.

Platinum-group elements

Science.gov (United States)

Zientek, Michael L.; Loferski, Patricia J.; Parks, Heather L.; Schulte, Ruth F.; Seal, Robert R.; Schulz, Klaus J.; DeYoung,, John H.; Seal, Robert R.; Bradley, Dwight C.

2017-12-19

The platinum-group elements (PGEs)—platinum, palladium, rhodium, ruthenium, iridium, and osmium—are metals that have similar physical and chemical properties and tend to occur together in nature. PGEs are indispensable to many industrial applications but are mined in only a few places. The availability and accessibility of PGEs could be disrupted by economic, environmental, political, and social events. The United States net import reliance as a percentage of apparent consumption is about 90 percent.PGEs have many industrial applications. They are used in catalytic converters to reduce carbon monoxide, hydrocarbon, and nitrous oxide emissions in automobile exhaust. The chemical industry requires platinum or platinum-rhodium alloys to manufacture nitric oxide, which is the raw material used to manufacture explosives, fertilizers, and nitric acid. In the petrochemical industry, platinum-supported catalysts are needed to refine crude oil and to produce aromatic compounds and high-octane gasoline. Alloys of PGEs are exceptionally hard and durable, making them the best known coating for industrial crucibles used in the manufacture of chemicals and synthetic materials. PGEs are used by the glass manufacturing industry in the production of fiberglass and flat-panel and liquid crystal displays. In the electronics industry, PGEs are used in computer hard disks, hybridized integrated circuits, and multilayer ceramic capacitors.Aside from their industrial applications, PGEs are used in such other fields as health, consumer goods, and finance. Platinum, for example, is used in medical implants, such as pacemakers, and PGEs are used in cancer-fighting drugs. Platinum alloys are an ideal choice for jewelry because of their white color, strength, and resistance to tarnish. Platinum, palladium, and rhodium in the form of coins and bars are also used as investment commodities, and various financial instruments based on the value of these PGEs are traded on major exchanges

Quantitative analysis of chemical elements in single cells using nuclear microprobe and nano-probe

International Nuclear Information System (INIS)

Deves, Guillaume

2010-01-01

The study of the role of trace elements at cellular level requires the use of state-of-the-art analytical tools that could achieve enough sensitivity and spatial resolution. We developed a new methodology for the accurate quantification of chemical element distribution in single cells based on a combination of ion beam analysis techniques STIM, PIXE and RBS. The quantification procedure relies on the development of a STIM data analysis software (Paparamborde). Validity of this methodology and limits are discussed here. The method allows the quantification of trace elements (μg/g) with a 19.8 % uncertainty in cellular compartments with mass below 0.1 ng. The main limit of the method lies in the poor number of samples that can be analyzed, due to long irradiation times required and limited access to ion beam analysis facilities. This is the reason why we developed a database for cellular chemical composition capitalization (BDC4). BDC4 has been designed in order to use cellular chemical composition as a tracer for biological activities and is expected to provide in the future reference chemical compositions for any cellular type or compartment. Application of the STIM-PIXE-RBS methodology to the study of nuclear toxicology of cobalt compounds is presented here showing that STIM analysis is absolutely needed when organic mass loss appears during PIXE-RBS irradiation. (author)

Toxic Release Inventory Chemicals by Groupings

Data.gov (United States)

U.S. Environmental Protection Agency — The Toxics Release Inventory (TRI) makes available information for more than 600 toxic chemicals that are being used, manufactured, treated, transported, or released...

Method of Improving Personal Name Search in Academic Information Service

Directory of Open Access Journals (Sweden)

Heejun Han

2012-12-01

Full Text Available All academic information on the web or elsewhere has its creator, that is, a subject who has created the information. The subject can be an individual, a group, or an institution, and can be a nation depending on the nature of the relevant information. Most information is composed of a title, an author, and contents. An essay which is under the academic information category has metadata including a title, an author, keyword, abstract, data about publication, place of publication, ISSN, and the like. A patent has metadata including the title, an applicant, an inventor, an attorney, IPC, number of application, and claims of the invention. Most web-based academic information services enable users to search the information by processing the meta-information. An important element is to search information by using the author field which corresponds to a personal name. This study suggests a method of efficient indexing and using the adjacent operation result ranking algorithm to which phrase search-based boosting elements are applied, and thus improving the accuracy of the search results of personal names. It also describes a method for providing the results of searching co-authors and related researchers in searching personal names. This method can be effectively applied to providing accurate and additional search results in the academic information services.

Elemental chemical characterization of coins of currently national circulating by X-ray fluorescence non-destructive techniques

International Nuclear Information System (INIS)

Olivera, Paula; Calcina, Esly

2013-01-01

Given the frequent counterfeit bills and coins is proposed in this paper to identify the elemental chemical composition; for now, the current official currencies circulating in our country, by Energy Dispersive X-ray Fluorescence technique and non-destructive methods, the goal is to compare with the false and establish the differences that could help identify them immediately taking advantage of the fast response of this technique. Have been identified the elements Al in the coins of 5 cents, Cu and Zn for 10 and 20 cents, Ni, Cu and Zn for 50 cents and a Un Nuevo Sol and Cr, Cu and Zn 2 coins 5 Nuevos Soles. 57 Peruvian coins of different production years and a counterfeit coin of 5 Nuevos Soles have been analyzed, finding Cu and Zn in central part and Fe in circulating edge ring, looking for this one the absence of Ni and Cr, which in the official currency was found. (authors).

The Chemistry of Superheavy Elements

CERN Document Server

Schädel, M

2003-01-01

The chemistry of transactinide or superheavy elements has reached element 108. Preparations are under way to leap to element 112 and beyond. The current status of this atom-at-a-time chemical research and its future perspectives are reviewed from an experimental point of view together with some of the interesting results from n -rich nuclides near and at the N=162 neutron shell. Experimental techniques and important results enlightening typical chemical properties of elements 104 through 108 are presented in an exemplary way. From the results of these experiments it is justified to place these elements in the Periodic Table of the Elements in to groups 4 through 8, respectively. However, mainly due to the influence of relativistic effects, it is no longer possible to deduce detailed chemical properties of these superheavy elements simply from this position.

Elemental analysis of pottery from Cerro de las Ventanas, Zacatecas, by INAA

Energy Technology Data Exchange (ETDEWEB)

Lopez del Rio, H.; Mireles G, F. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Calle Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico); Mendez C, R. Y. [Universidad Autonoma de Zacatecas, Unidad Academica de Antropologia, Apdo. Postal 555 Suc. C, Zacatecas (Mexico); Nicolas C, M. [Universidad Autonoma de San Luis Potosi, Coordinacion de Ciencias Sociales y Humanidades, Av. Industrias 101-A, Fracc. Talleres, 78494 San Luis Potosi (Mexico); Speakman, R. J. [Museum Conservation Institute, Smithsonian Institution, Suitland, 20746 Maryland (United States); Glascock, M. D. [Reactor Center, University of Missouri, Columbia, 65211 Missouri (United States)

2009-10-15

Fifteen ceramic fragments samples from Cerro de las Ventanas site, Zacatecas, were analyzed by instrumental neutron activation analysis. Thirty-two elements were measured: Al, As, Ba, Ca, Ce, Co, Cr, Cs, Dy, Eu, Fe, Hf, K, La, Lu, Mn, Na, Nd, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Ti, Th, U, V, Yb, Zn, and Zr. Cluster analysis and principal component analysis were performed on the dataset to examine similarities between samples and to establish compositional groups. The statistical analyses of the dataset suggest that the pottery samples form a unique chemically homogeneous group, with the exception of one pottery sample. The compositional data were compared to an existing Meso american ceramic database. It was found that the newly generated data fit best with data from a previous chemical analysis of pottery from the Mal paso Valley. However, despite the apparent similarity, pottery samples from the site of Cerro de las Ventanas represent a new and unique chemical fingerprint in the region. (Author)

Elemental analysis of pottery from Cerro de las Ventanas, Zacatecas, by INAA

International Nuclear Information System (INIS)

Lopez del Rio, H.; Mireles G, F.; Mendez C, R. Y.; Nicolas C, M.; Speakman, R. J.; Glascock, M. D.

2009-10-01

Fifteen ceramic fragments samples from Cerro de las Ventanas site, Zacatecas, were analyzed by instrumental neutron activation analysis. Thirty-two elements were measured: Al, As, Ba, Ca, Ce, Co, Cr, Cs, Dy, Eu, Fe, Hf, K, La, Lu, Mn, Na, Nd, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Ti, Th, U, V, Yb, Zn, and Zr. Cluster analysis and principal component analysis were performed on the dataset to examine similarities between samples and to establish compositional groups. The statistical analyses of the dataset suggest that the pottery samples form a unique chemically homogeneous group, with the exception of one pottery sample. The compositional data were compared to an existing Meso american ceramic database. It was found that the newly generated data fit best with data from a previous chemical analysis of pottery from the Mal paso Valley. However, despite the apparent similarity, pottery samples from the site of Cerro de las Ventanas represent a new and unique chemical fingerprint in the region. (Author)

Chemical Safety Vulnerability Working Group report. Volume 3

Energy Technology Data Exchange (ETDEWEB)

1994-09-01

The Chemical Safety Vulnerability (CSV) Working Group was established to identify adverse conditions involving hazardous chemicals at DOE facilities that might result in fires or explosions, release of hazardous chemicals to the environment, or exposure of workers or the public to chemicals. A CSV Review was conducted in 148 facilities at 29 sites. Eight generic vulnerabilities were documented related to: abandoned chemicals and chemical residuals; past chemical spills and ground releases; characterization of legacy chemicals and wastes; disposition of legacy chemicals; storage facilities and conditions; condition of facilities and support systems; unanalyzed and unaddressed hazards; and inventory control and tracking. Weaknesses in five programmatic areas were also identified related to: management commitment and planning; chemical safety management programs; aging facilities that continue to operate; nonoperating facilities awaiting deactivation; and resource allocations. Volume 3 consists of eleven appendices containing the following: Field verification reports for Idaho National Engineering Lab., Rocky Flats Plant, Brookhaven National Lab., Los Alamos National Lab., and Sandia National Laboratories (NM); Mini-visits to small DOE sites; Working Group meeting, June 7--8, 1994; Commendable practices; Related chemical safety initiatives at DOE; Regulatory framework and industry initiatives related to chemical safety; and Chemical inventory data from field self-evaluation reports.

Chemical Safety Vulnerability Working Group report. Volume 3

International Nuclear Information System (INIS)

1994-09-01

The Chemical Safety Vulnerability (CSV) Working Group was established to identify adverse conditions involving hazardous chemicals at DOE facilities that might result in fires or explosions, release of hazardous chemicals to the environment, or exposure of workers or the public to chemicals. A CSV Review was conducted in 148 facilities at 29 sites. Eight generic vulnerabilities were documented related to: abandoned chemicals and chemical residuals; past chemical spills and ground releases; characterization of legacy chemicals and wastes; disposition of legacy chemicals; storage facilities and conditions; condition of facilities and support systems; unanalyzed and unaddressed hazards; and inventory control and tracking. Weaknesses in five programmatic areas were also identified related to: management commitment and planning; chemical safety management programs; aging facilities that continue to operate; nonoperating facilities awaiting deactivation; and resource allocations. Volume 3 consists of eleven appendices containing the following: Field verification reports for Idaho National Engineering Lab., Rocky Flats Plant, Brookhaven National Lab., Los Alamos National Lab., and Sandia National Laboratories (NM); Mini-visits to small DOE sites; Working Group meeting, June 7--8, 1994; Commendable practices; Related chemical safety initiatives at DOE; Regulatory framework and industry initiatives related to chemical safety; and Chemical inventory data from field self-evaluation reports

Results of the experiment on chemical identification of Db as a decay product of element 115

International Nuclear Information System (INIS)

Dmitriev, S.N.; Oganesyan, Yu.Ts.; Utenkov, V.K.

2004-01-01

For the first time the chemical identification of Db as the terminal isotope of the decay element 115 produced via the 243 Am( 48 Ca, 3n) 288 115 reaction was realized. The experiment was performed on the U400 cyclotron of FLNR, JINR. The 243 Am target was bombarded with a beam dose of 3.4 · 10 18 48 Ca projectiles at an energy of 247 MeV in the center of the target. The reaction products were collected in the surface of a copper catcher block, which was removed with a lathe and then dissolved in concentrated HNO 3 . The group 5 elements were separated by sorption onto Dowex 50X8 cation-exchange resin with subsequent desorption using 1 M HF, which forms anionic fluoride complexes of group 5 elements. The eluant was evaporated onto 0.4 μm thick polyethylene foils which were placed between a pair of semiconductor detectors surrounded by 3 He neutron counters for measurement of α particles, fission fragments and neutrons. Over the course of the experiment, we observed 15 spontaneous fission events with T 1/2 = 32 -7 +11 h which we attribute to 268 Db. The production cross section for the 243 Am + 48 Ca reaction was 4.2 -1.2 + 1 .6 pb. These results agree with the original element 115 synthesis experiment where 268 Db was first observed as the terminal isotope following the five consecutive α decays from the 288 115 parent nucleus at the Dubna gas-filled separator. The data from the present experiment give independent evidence for the synthesis of element 115 as well as element 113 via the 243 Am + 48 Ca reaction

Nuclear analytical methods for platinum group elements

International Nuclear Information System (INIS)

2005-04-01

Platinum group elements (PGE) are of special interest for analytical research due to their economic importance like chemical peculiarities as catalysts, medical applications as anticancer drugs, and possible environmental detrimental impact as exhaust from automobile catalyzers. Natural levels of PGE are so low in concentration that most of the current analytical techniques approach their limit of detection capacity. In addition, Ru, Rh, Pd, Re, Os, Ir, and Pt analyses still constitute a challenge in accuracy and precision of quantification in natural matrices. Nuclear analytical techniques, such as neutron activation analysis, X ray fluorescence, or proton-induced X ray emission (PIXE), which are generally considered as reference methods for many analytical problems, are useful as well. However, due to methodological restrictions, they can, in most cases, only be applied after pre-concentration and under special irradiation conditions. This report was prepared following a coordinated research project and a consultants meeting addressing the subject from different viewpoints. The experts involved suggested to discuss the issue according to the (1) application, hence, the concentration levels encountered, and (2) method applied for analysis. Each of the different fields of application needs special consideration for sample preparation, PGE pre-concentration, and determination. Additionally, each analytical method requires special attention regarding the sensitivity and sample type. Quality assurance/quality control aspects are considered towards the end of the report. It is intended to provide the reader of this publication with state-of-the-art information on the various aspects of PGE analysis and to advise which technique might be most suitable for a particular analytical problem related to platinum group elements. In particular, many case studies described in detail from the authors' laboratory experience might help to decide which way to go. As in many cases

Investigation on trace and major elements in anti-asthmatic medicinal plants by PIXE and PIGE techniques

Science.gov (United States)

Bhanisana Devi, R. K.; Nandakumar Sarma, H.; Kumar, Sanjiv

2015-01-01

Five widely used anti-asthmatic medicinal plants of north-eastern region of India have been investigated by using Proton Induced X-ray Emission (PIXE) and Proton Induced Gamma ray Emission (PIGE) techniques. The elements namely K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se and Br were detected with different concentrations (in ppm level) by PIXE technique whereas light elements namely F, Na, Mg, Al, P and Cl by PIGE technique in the studied plants. No toxic heavy metals such as Hg, Pb, Cd were detected. Analysis was performed on thick targets (pellets) prepared using the powders of specimens through a series of processing steps. Thick targets of plant based Certified Reference Materials (CRMs) were served as standardization of PIXE and PIGE set up. The trace elements present in the studied plants have been correlated with their medicinal properties.

Investigation on trace and major elements in anti-asthmatic medicinal plants by PIXE and PIGE techniques

Energy Technology Data Exchange (ETDEWEB)

Bhanisana Devi, R.K., E-mail: bhanisanark@gmail.com [Department of Physics, Manipur University, Canchipur 795003 (India); Nandakumar Sarma, H. [Department of Physics, Manipur University, Canchipur 795003 (India); Kumar, Sanjiv [National Centre for Compositional Characterization of Materials (NCCCM), Hyderabad 500062 (India)

2015-01-15

Five widely used anti-asthmatic medicinal plants of north-eastern region of India have been investigated by using Proton Induced X-ray Emission (PIXE) and Proton Induced Gamma ray Emission (PIGE) techniques. The elements namely K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se and Br were detected with different concentrations (in ppm level) by PIXE technique whereas light elements namely F, Na, Mg, Al, P and Cl by PIGE technique in the studied plants. No toxic heavy metals such as Hg, Pb, Cd were detected. Analysis was performed on thick targets (pellets) prepared using the powders of specimens through a series of processing steps. Thick targets of plant based Certified Reference Materials (CRMs) were served as standardization of PIXE and PIGE set up. The trace elements present in the studied plants have been correlated with their medicinal properties.

[Bioinorganic chemical composition of the lens and methods of its investigation].

Science.gov (United States)

Avetisov, S E; Novikov, I A; Pakhomova, N A; Motalov, V G

2018-01-01

Bioinorganic chemical composition of the lens of human and experimental animals (cows, dogs, rats, rabbits) have been analyzed in various studies. In most cases, the studies employed different methods to determine the gross (total) composition of chemical elements and their concentrations in the examined samples. Less frequently, they included an assessment of the distribution of chemical elements in the lens and correlation of their concentration with its morphological changes. Chemical elements from all groups (series) of the periodic classification system were discovered in the lens substance. Despite similar investigation methods, different authors obtained contradicting results on the chemical composition of the lens. This article presents data suggesting possible correlation between inorganic chemical elements in the lens substance with the development and formation of lenticular opacities. All currently employed methods are known to only analyze limited number of select chemical elements in the tissues and do not consider the whole range of elements that can be analyzed with existing technology; furthermore, the majority of studies are conducted on the animal model lens. Therefore, it is feasible to continue the development of the chemical microanalysis method by increasing the sensitivity of Scanning Electron Microscopy with Energy Dispersive Spectroscopy (SEM/EDS) with the purpose of assessing the gross chemical composition and distribution of the elements in the lens substance, as well as revealing possible correlation between element concentration and morphological changes in the lens.

Parallel and serial grouping of image elements in visual perception

NARCIS (Netherlands)

Houtkamp, R.; Roelfsema, P.R.

2010-01-01

The visual system groups image elements that belong to an object and segregates them from other objects and the background. Important cues for this grouping process are the Gestalt criteria, and most theories propose that these are applied in parallel across the visual scene. Here, we find that

Exposure assessment of a cyclist to particles and chemical elements.

Science.gov (United States)

Ramos, C A; Silva, J R; Faria, T; Wolterbeek, T H; Almeida, S M

2017-05-01

Cycle paths can be used as a route for active transportation or simply to cycle for physical activity and leisure. However, exposure to air pollutants can be boosted while cycling, in urban environments, due to the proximity to vehicular emissions and elevated breathing rates. The objective of this work was to assess the exposure of a cyclist to particles and to chemical elements by combining real-time aerosol mass concentration reading equipment and biomonitoring techniques. PM 10 and PM 2.5 were measured on three cycle paths located in Lisbon, during weekdays and weekends and during rush hours and off-peak hours resulting in a total of 60 campaigns. Lichens were exposed along cycle paths for 3 months, and their element contents were measured by instrumental neutron activation analysis using the k 0 methodology (k 0 -INAA). Using a bicycle commute route of lower traffic intensity and avoiding rush hours or other times with elevated vehicular congestion facilitate a reduction in exposure to pollutants. The implementation of cycle paths in cities is important to stimulate physical activity and active transportation; however, it is essential to consider ambient air and pollutant sources to create safer infrastructures.

Selecting chemical and ecotoxicological test batteries for risk assessment of trace element-contaminated soils (phyto)managed by gentle remediation options (GRO).

Science.gov (United States)

Kumpiene, Jurate; Bert, Valérie; Dimitriou, Ioannis; Eriksson, Jan; Friesl-Hanl, Wolfgang; Galazka, Rafal; Herzig, Rolf; Janssen, Jolien; Kidd, Petra; Mench, Michel; Müller, Ingo; Neu, Silke; Oustriere, Nadège; Puschenreiter, Markus; Renella, Giancarlo; Roumier, Pierre-Hervé; Siebielec, Grzegorz; Vangronsveld, Jaco; Manier, Nicolas

2014-10-15

During the past decades a number of field trials with gentle remediation options (GRO) have been established on trace element (TE) contaminated sites throughout Europe. Each research group selects different methods to assess the remediation success making it difficult to compare efficacy between various sites and treatments. This study aimed at selecting a minimum risk assessment battery combining chemical and ecotoxicological assays for assessing and comparing the effectiveness of GRO implemented in seven European case studies. Two test batteries were pre-selected; a chemical one for quantifying TE exposure in untreated soils and GRO-managed soils and a biological one for characterizing soil functionality and ecotoxicity. Soil samples from field studies representing one of the main GROs (phytoextraction in Belgium, Sweden, Germany and Switzerland, aided phytoextraction in France, and aided phytostabilization or in situ stabilization/phytoexclusion in Poland, France and Austria) were collected and assessed using the selected test batteries. The best correlations were obtained between NH4NO3-extractable, followed by NaNO3-extractable TE and the ecotoxicological responses. Biometrical parameters and biomarkers of dwarf beans were the most responsive indicators for the soil treatments and changes in soil TE exposures. Plant growth was inhibited at the higher extractable TE concentrations, while plant stress enzyme activities increased with the higher TE extractability. Based on these results, a minimum risk assessment battery to compare/biomonitor the sites phytomanaged by GROs might consist of the NH4NO3 extraction and the bean Plantox test including the stress enzyme activities. Copyright © 2014 Elsevier B.V. All rights reserved.

A class of chemical pinning centers including two elements foreign to HTS

Energy Technology Data Exchange (ETDEWEB)

Weinstein, Roy; Sawh, Ravi-Persad

2003-01-01

Very small deposits are formed when two foreign elements, A and B, are added to textured (RE)BCO. These deposits increase the J{sub c} of samples and hence the maximum trapped field. Deposit sizes are generally in the range 200-400 nm. Their chemical composition is (A{sub x},B{sub y})(RE)Ba{sub 2}O{sub 6}, where x+y=1 and x=y{+-}0.1. Their structure is double perovskite. The deposits produce two types of pinning, one by refinement (e.g., of the Y211 phase) and the other due to the double perovskite deposits themselves. In those cases tested, the refinement increases J{sub c} by factors exceeding 1.33, and the deposits increase J{sub c} by factors exceeding 2, for a total increase by a factor exceeding 2.66. Element A can be U, W or Mo. Element B can be Pt or Zr. We speculate on possible additional elements in classes A and B.

On the enrichment of low-abundant isotopes of light chemical elements by gas centrifuges

International Nuclear Information System (INIS)

Borisevich, V.D.; Morozov, O.E.; Zaozerskiy, Yu.P.; Shmelev, G.M.; Shipilov, Yu.D.

2000-01-01

A brief review of the main areas for the application of the isotopes 15 N and 13 C is made. Separation of the nitrogen isotopes in a single gas centrifuge in the form of pure nitrogen, ammonia, and trifluoride of nitrogen as well as the carbon isotopes in the form of carbon dioxide has been studied by means of numerical simulation. The parameters of the centrifugal machine investigated were close to the parameters of the Iguassu machine. The dependence of the efficiency criterion versus the basic parameters of the separation process has been explored in the computational experiments. Comparisons of the calculated results with the experimental data have shown good agreement. The results obtained have demonstrated the possibility of using gas centrifuge technology to enrich successfully the low-abundant isotopes of light chemical elements

Clustering of samples and elements based on multi-variable chemical data

International Nuclear Information System (INIS)

Op de Beeck, J.

1984-01-01

Clustering and classification are defined in the context of multivariable chemical analysis data. Classical multi-variate techniques, commonly used to interpret such data, are shown to be based on probabilistic and geometrical principles which are not justified for analytical data, since in that case one assumes or expects a system of more or less systematically related objects (samples) as defined by measurements on more or less systematically interdependent variables (elements). For the specific analytical problem of data set concerning a large number of trace elements determined in a large number of samples, a deterministic cluster analysis can be used to develop the underlying classification structure. Three main steps can be distinguished: diagnostic evaluation and preprocessing of the raw input data; computation of a symmetric matrix with pairwise standardized dissimilarity values between all possible pairs of samples and/or elements; and ultrametric clustering strategy to produce the final classification as a dendrogram. The software packages designed to perform these tasks are discussed and final results are given. Conclusions are formulated concerning the dangers of using multivariate, clustering and classification software packages as a black-box

Magnetically assisted chemical separation (MACS) process: Preparation and optimization of particles for removal of transuranic elements

International Nuclear Information System (INIS)

Nunez, L.; Kaminski, M.; Bradley, C.; Buchholz, B.A.; Aase, S.B.; Tuazon, H.E.; Vandegrift, G.F.; Landsberger, S.

1995-05-01

The Magnetically Assisted Chemical Separation (MACS) process combines the selectivity afforded by solvent extractants with magnetic separation by using specially coated magnetic particles to provide a more efficient chemical separation of transuranic (TRU) elements, other radionuclides, and heavy metals from waste streams. Development of the MACS process uses chemical and physical techniques to elucidate the properties of particle coatings and the extent of radiolytic and chemical damage to the particles, and to optimize the stages of loading, extraction, and particle regeneration. This report describes the development of a separation process for TRU elements from various high-level waste streams. Polymer-coated ferromagnetic particles with an adsorbed layer of octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) diluted with tributyl phosphate (TBP) were evaluated for use in the separation and recovery of americium and plutonium from nuclear waste solutions. Due to their chemical nature, these extractants selectively complex americium and plutonium contaminants onto the particles, which can then be recovered from the solution by using a magnet. The partition coefficients were larger than those expected based on liquid[liquid extractions, and the extraction proceeded with rapid kinetics. Extractants were stripped from the particles with alcohols and 400-fold volume reductions were achieved. Particles were more sensitive to acid hydrolysis than to radiolysis. Overall, the optimization of a suitable NMCS particle for TRU separation was achieved under simulant conditions, and a MACS unit is currently being designed for an in-lab demonstration

Synthesis of Y2O3: Eu added the group 1 or 2 elements using complex-polymerization and its luminescent properties

International Nuclear Information System (INIS)

Park, Sang Mi; Jang, Ho G.; Kim, Chang Hae; Park, Joung Kyu; Park, Hee Dong

2001-01-01

Europium activated yttrium oxide (Y 2 O 3 :Eu) is extensively applied to red phosphor for Flat Panel Display because of its high efficiency and the thermal and chemical stability. Flat Panel Display screen which have a high resolution and high efficiency needs to the phosphors of ideally small size spherical particle. In this study, we prepared a Y 2 O 3 :Eu phosphor using polymeric precursor methods and investigated the codoping effect by introducing the group 1 or 2 elements to Y 2 O 3 :Eu phosphor in view of improvement of luminance efficiency

Elemental distribution imaging by energy-filtering transmission electron microscopy (EFTEM) and its applications

International Nuclear Information System (INIS)

Kurata, Hiroki

1996-01-01

EFTEM is new microscopy with the object of visualizing high resolution quantitative elemental distribution. The measurement principles and the present state of EFTEM studies are explained by the examples of measurement of the elemental distributions. EFTEM is a combination of the transmission electron microscope with the electron energy loss spectroscopy (EFLS). EFTEM method sets the slit in the specific energy field and put the electron passing the slit back in the microscopic image. The qualitative elemental analysis is obtained by observing the position of the absorption end of core electronic excitation spectrum and the quantitative one by determining the core electronic excitation strength of the specific atom depend on filtering with energy selector slit. The binding state and the local structure in the neighborhood of excited atom is determined by the fine structure of absorption end. By the chemical mapping method, the distribution image of chemical binding state is visualized by the imaging chemical map obtained by filtering the specific peak strength of fine structure with the narrow energy selector slit. The fine powder of lead chromate (PbCrO 4 ) covered with silica glass was shown as a typical example of the elemental distribution image of core electronic excitation spectrum. The quantitative analysis method of elemental distribution image is explained. The possibility of single atom analysis at nanometer was shown by the example of nanotube observed by EFTEM. (S.Y.)

Effects of Responding to a Name and Group Call on Preschoolers' Compliance

Science.gov (United States)

Beaulieu, Lauren; Hanley, Gregory P.; Roberson, Aleasha A.

2012-01-01

We assessed teacher-child relations with respect to children's name calls, instructions, and compliance in a preschool classroom. The most frequent consequence to a child's name being called was the provision of instructions. We also observed a higher probability of compliance when children attended to a name call. Next, we evaluated the effects…

Mineralogy and chemical composition and distribution of rare earth elements of clay-rich sediments, Central Uganda

International Nuclear Information System (INIS)

Nyakairu, G.W.A.

2001-02-01

In Uganda, Precambrian rocks are extensively weathered to sediments, which are locally altered to form considerable clay deposits. Clay-rich sediment samples were collected from the Kajjansi, Kitiko, Kitetika, and Ntawo valleys (central Uganda), all of which are currently used for traditional brick, tile, and pottery manufacture. The mineralogical and chemical characteristics, and source rocks of these clay-rich sediments is not well understood. A study using modern analytical techniques, such as XRD, to obtain the bulk mineralogical composition, and XRF and INAA analyses for whole rock major and trace element abundances was performed. The results show that the sediments are dominated by kaolinite and quartz, and minor phases include smectite, chlorite, and illite/muscovite. Whole rock chemistry shows that sediment samples rich in SiO2 have low Al, Fe, Sc and Cr contents. The high chemical index of alteration (CIA) values (87 to 96), chemical index of weathering (CIW) values around 98 and low contents of the alkali and alkali earth elements of the clay-rich sediments suggest a relatively more intense weathering source area. The clay-rich sediments as raw materials for industry were classified as silty clays from grain size analysis. The chemical and mineralogical composition results show that, taken as a whole, the clay-rich sediments possess characteristics satisfactory for brick production. The chondrite-normalized rare earth elements (REE) patterns of the clay-rich sediments show LREE enrichments and a negative Eu anomaly. The high chondrite-normalized La/Yb ratios, and Gd/Yb ratios lower than 2.0, confirm that the sediments are enriched in the LREEs. The mineralogical composition, REE contents, and elemental ratios in these sediments suggest a provenance from mainly felsic rocks, with only minor contributions from basic sources. The basic sediments were most likely derived from metasedimentary rocks, such as muscovite-biotite schists, which are characteristic

Investigation of Chemical and Physical Changes to Bioapatite During Fossilization Using Trace Element Geochemistry, Infrared Spectroscopy and Stable Isotopes

Science.gov (United States)

Suarez, C. A.; Kohn, M. J.

2013-12-01

Bioapatite in the form of vertebrate bone can be used for a wide variety of paleo-proxies, from determination of ancient diet to the isotopic composition of meteoric water. Bioapatite alteration during diagenesis is a constant barrier to the use of fossil bone as a paleo-proxy. To elucidate the physical and chemical alteration of bone apatite during fossilization, we analyzed an assortment of fossil bones of different ages for trace elements, using LA-ICP-MS, stable isotopes, and reflected IR spectroscopy. One set of fossil bones from the Pleistocene of Idaho show a diffusion recrystallization profile, however, rare earth element (REE) profiles indicate diffusion adsorption. This suggests that REE diffusion is controlled by changing (namely decreasing) boundary conditions (i.e. decreasing concentration of REE in surrounding pore fluids). Reflected IR analysis along this concentration profile reveal that areas high in U have lost type A carbonate from the crystal structure in addition to water and organics. Stable isotopic analysis of carbon and oxygen will determine what, if any, change in the isotopic composition of the carbonate component of apatite has occurred do to the diffusion and recrystallization process. Analysis of much older bone from the Cretaceous of China reveal shallow REE and U concentration profiles and very uniform reflected IR spectra with a significant loss of type A carbonate throughout the entire bone cortex. Analysis of stable isotopes through the bone cortex will be compared to the stable isotopes collected from the Pleistocene of Idaho.

Molecules and Models The molecular structures of main group element compounds

CERN Document Server

Haaland, Arne

2008-01-01

This book provides a systematic description of the molecular structures and bonding in simple compounds of the main group elements with particular emphasis on bond distances, bond energies and coordination geometries. The description includes the structures of hydrogen, halogen and methyl derivatives of the elements in each group, some of these molecules are ionic, some polar covalent. The survey of molecules whose structures conform to well-established trends is followed byrepresentative examples of molecules that do not conform. We also describe electron donor-acceptor and hydrogen bonded co

Diversity of Chemical Bonding and Oxidation States in MS ₄ Molecules of Group 8 Elements

Energy Technology Data Exchange (ETDEWEB)

Huang, Wei [Department of Chemistry and Key Laboratory of Organic Optoelectronics & Molecular Engineering of the Ministry of Education, Tsinghua University, Beijing 100084 P.R. China; Jiang, Ning [Department of Chemistry and Key Laboratory of Organic Optoelectronics & Molecular Engineering of the Ministry of Education, Tsinghua University, Beijing 100084 P.R. China; Schwarz, W. H. Eugen [Department of Chemistry and Key Laboratory of Organic Optoelectronics & Molecular Engineering of the Ministry of Education, Tsinghua University, Beijing 100084 P.R. China; Physical and Theoretical Chemistry, University of Siegen, Siegen 57068 Germany; Yang, Ping [Theoretical Division, Los Alamos National Laboratory, Los Alamos New Mexico 87545 USA; Environmental Molecular Science Laboratory, Pacific Northwest National Laboratory, Richland Washington 953002 USA; Li, Jun [Department of Chemistry and Key Laboratory of Organic Optoelectronics & Molecular Engineering of the Ministry of Education, Tsinghua University, Beijing 100084 P.R. China; Environmental Molecular Science Laboratory, Pacific Northwest National Laboratory, Richland Washington 953002 USA

2017-07-11

The geometric and electronic ground-state structures of six MS₄ molecules (M = group-8 metals Fe, Ru, Os, Hs, Sm, and Pu) have been studied by using quantum-chemical density-functional and correlated wave-function approaches. The MS₄ species are compared to analogous MO₄ species recently investi-gated (Inorg. Chem. 2016, 55: 4616). Metal oxidation state (MOS) of high value VIII appears in low- spin singlet Td geometric species (Os,Hs)S₄ and (Ru,Os,Hs)O₄, whereas low MOS=II appears in high- spin septet D_2d species Fe(S₂)₂ and (slightly excited) metastable Fe(O₂)₂. The ground states of all other molecules have intermediate MOS values, containing S^2-, S₂^2-, S2^1- (and resp. O^2--, O^1-, O₂^2-, O₂^1-) ligands, bonded by ionic, covalent and correlative contributions.

Trace-element analysis of Antarctic H chondrites: Chemical weathering and comparisons with their non-Antarctic counterparts

International Nuclear Information System (INIS)

Kwok, J.E.

1986-01-01

Large numbers of meteorites have been discovered in Antarctica over the last decade (7000 fragments probably representing over 1200 separate events). They are important for their numbers and for their complement of unique or rare specimens; they also have long terrestrial ages (up to 1,000,000 years) compared to non-Antarctic falls (usually < 200 years). We report compositional data for mobile/volatile trace elements Ag, Au, Bi, Cd, Co, Cs, In, Rb, Sb, Se, Te, Ti, U, and Zn in a suite of Antarctic H chondrites. Our data show that heavily oxidized H chondrites are leached of a portion of their trace elements and, therefore, have been chemically compromised by their stay in Antarctica. The less oxidized specimens seem to have retained their chemical integrity. We suggest possibilities for using chemical data to measure the degree of a chondrite's chemical weathering. We compare our data to that obtained previously for non-Antarctic H chondrites (Linger et al., 1986), by petrologic type (H4, H5, H6, H4-6) and shock-loading (moderately shocked facies a-c, heavily shocked facies d-f). Many statistically significant differences are found between non-Antarctic and Victoria Land, Antarctica H chondrites of each petrologic type and of shock facies d-f

The platinum group elements and gold: analysis by radiochemical and instrumental neutron activation analysis and relevance to geological exploration and related problems

Energy Technology Data Exchange (ETDEWEB)

Reeves, S; Plimer, I R [Melbourne Univ., Parkville, VIC (Australia). School of Physics

1997-12-31

This paper presents an overview of research conducted with the support of the Australian Institute of Nuclear Science and Engineering, at the University of Melbourne, School of Earth Sciences, Radiochemical Neutron Activation Laboratory. The primary objective of this research is to realize the high potential of the platinum group elements (PGE) and gold to the solution of petrogenetic problems, the study of magma generation and magmatic processes in mafic/ultramafic rock suites, as tracers in hydrothermal ore formation. The PGEs (Os, Ru, Ir, Pt, Pd and Rh) are among the least abundant of all elements on earth with unique properties such as high melting points, high electrical and thermal conductivity, high density, strength and toughness as alloys. They exhibit both siderophile and chalcophile characteristics and are valuable tools in providing information about magmatic processes, in particular S-saturation, as well as crystal fractionation trends. Two distinct groups of PGEs are discerned; the IPGEs (Ru, Os, Ir) and the PPGEs (Pt, Pd, Rh, Au) on the basis of their behaviour during fractionation processes. Using chondrite normalized PGE patterns it is possible to distinguish between sulphides that segregated from primitive magmas, such as komatiites, and sulphides which segregated from more fractionated magmas, such as tholeiites. It is critical to the understanding of these processes to be able to analyse key elements, such as the PGE and gold, in the parts per billion to parts per trillion range. Platinum group elements and Au were determined by radiochemical neutron activation analysis using a modified NiS fire-assay preconcentration technique, adapted from procedures first used by Robert, R.V. D. and van Wyk, E. (1975) . Detection limits are generally 0.005-0.01 ppb (Au and Ir), 0.1-0.2 ppb (Pd and Pt), and 0.1-0.5 ppb for Ru. 9 refs.

The platinum group elements and gold: analysis by radiochemical and instrumental neutron activation analysis and relevance to geological exploration and related problems

Energy Technology Data Exchange (ETDEWEB)

Reeves, S.; Plimer, I. R. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

1996-12-31

This paper presents an overview of research conducted with the support of the Australian Institute of Nuclear Science and Engineering, at the University of Melbourne, School of Earth Sciences, Radiochemical Neutron Activation Laboratory. The primary objective of this research is to realize the high potential of the platinum group elements (PGE) and gold to the solution of petrogenetic problems, the study of magma generation and magmatic processes in mafic/ultramafic rock suites, as tracers in hydrothermal ore formation. The PGEs (Os, Ru, Ir, Pt, Pd and Rh) are among the least abundant of all elements on earth with unique properties such as high melting points, high electrical and thermal conductivity, high density, strength and toughness as alloys. They exhibit both siderophile and chalcophile characteristics and are valuable tools in providing information about magmatic processes, in particular S-saturation, as well as crystal fractionation trends. Two distinct groups of PGEs are discerned; the IPGEs (Ru, Os, Ir) and the PPGEs (Pt, Pd, Rh, Au) on the basis of their behaviour during fractionation processes. Using chondrite normalized PGE patterns it is possible to distinguish between sulphides that segregated from primitive magmas, such as komatiites, and sulphides which segregated from more fractionated magmas, such as tholeiites. It is critical to the understanding of these processes to be able to analyse key elements, such as the PGE and gold, in the parts per billion to parts per trillion range. Platinum group elements and Au were determined by radiochemical neutron activation analysis using a modified NiS fire-assay preconcentration technique, adapted from procedures first used by Robert, R.V. D. and van Wyk, E. (1975) . Detection limits are generally 0.005-0.01 ppb (Au and Ir), 0.1-0.2 ppb (Pd and Pt), and 0.1-0.5 ppb for Ru. 9 refs.

The platinum group elements and gold: analysis by radiochemical and instrumental neutron activation analysis and relevance to geological exploration and related problems

International Nuclear Information System (INIS)

Reeves, S.; Plimer, I. R.

1996-01-01

This paper presents an overview of research conducted with the support of the Australian Institute of Nuclear Science and Engineering, at the University of Melbourne, School of Earth Sciences, Radiochemical Neutron Activation Laboratory. The primary objective of this research is to realize the high potential of the platinum group elements (PGE) and gold to the solution of petrogenetic problems, the study of magma generation and magmatic processes in mafic/ultramafic rock suites, as tracers in hydrothermal ore formation. The PGEs (Os, Ru, Ir, Pt, Pd and Rh) are among the least abundant of all elements on earth with unique properties such as high melting points, high electrical and thermal conductivity, high density, strength and toughness as alloys. They exhibit both siderophile and chalcophile characteristics and are valuable tools in providing information about magmatic processes, in particular S-saturation, as well as crystal fractionation trends. Two distinct groups of PGEs are discerned; the IPGEs (Ru, Os, Ir) and the PPGEs (Pt, Pd, Rh, Au) on the basis of their behaviour during fractionation processes. Using chondrite normalized PGE patterns it is possible to distinguish between sulphides that segregated from primitive magmas, such as komatiites, and sulphides which segregated from more fractionated magmas, such as tholeiites. It is critical to the understanding of these processes to be able to analyse key elements, such as the PGE and gold, in the parts per billion to parts per trillion range. Platinum group elements and Au were determined by radiochemical neutron activation analysis using a modified NiS fire-assay preconcentration technique, adapted from procedures first used by Robert, R.V. D. and van Wyk, E. (1975) . Detection limits are generally 0.005-0.01 ppb (Au and Ir), 0.1-0.2 ppb (Pd and Pt), and 0.1-0.5 ppb for Ru. 9 refs

Gardner's commercially important chemicals: synonyms, trade names, and properties

National Research Council Canada - National Science Library

Milne, George W. A

2005-01-01

... provided for individual chemical compounds. Book In the preparation of this an effort has been made to include useful information on chemicals that play a significant role in commerce. The US Environmental Protection Agency (EPA), in cooperation with industry, maintains a list of "High Production Volume" (HPV) chemicals whose productio...

Structural alterations in rat myocardium induced by chronic l-arginine and l-NAME supplementation

Directory of Open Access Journals (Sweden)

Amal Abdussalam Ali A. Hmaid

2018-03-01

Full Text Available Structural changes affecting cardiomyocyte function may contribute to the pathophysiological remodeling underlying cardiac function impairment. Recent reports have shown that endogenous nitric oxide (NO plays an important role in this process. In order to examine the role of NO in cardiomyocyte remodeling, male rats were acclimated to room temperature (22 ± 1 °C or cold (4 ± 1 °C and treated with 2.25% l-arginine·HCl or 0.01% l-NAME (Nω-nitro-l-arginine methyl ester·HCl for 45 days. Untreated groups served as controls. Right heart ventricles were routinely prepared for light microscopic examination. Stereological estimations of volume densities of cardiomyocytes, surrounding blood vessels and connective tissue, as well as the morphometric measurements of cardiomyocyte diameters were performed. Tissue sections were also analyzed for structural alterations. We observed that both l-arginine and l-NAME supplementation induced cardiomyocyte hypertrophy, regardless of ambient temperature. However, cardiomyocyte hypertrophy was associated with fibrosis and extra collagen deposition only in the l-NAME treated group. Taken together, our results suggest that NO has a modulatory role in right heart ventricle remodeling by coordinating hypertrophy of cardiomyocytes and fibrous tissue preventing cardiac fibrosis. Keywords: Cardiomyocyte, Cardiac hypertrophy, l-Arginine, l-NAME, Myocardium

Selected elements and organic chemicals in bed sediment and fish tissue of the Tualatin River basin, Oregon, 1992-96

Science.gov (United States)

Bonn, Bernadine A.

1999-01-01

A variety of elements and organic compounds have entered the environment as a result of human activities. Such substances find their way to aquatic sediments from direct discharges to waterways, atmospheric emissions, and runoff. Some of these chemicals are known to harm fish or wildlife, either by direct toxicity, by reducing viability, or by limiting reproductive success. In aquatic systems, sediments become the eventual sink for most of these chemicals. Analyzing the sediments provides a first step in a chemical inventory that can lead to an assessment of potential biological impacts (Kennicutt and others, 1994).

Morphology and chemical characteristics of micro- and Nano-particles in the haze in Beijing studied by XPS and TEM/EDX

Energy Technology Data Exchange (ETDEWEB)

Xu, Peng [Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, Key Laboratory of Advanced Functional Materials, Education Ministry of China, and Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124 (China); CAS Key Laboratory of Standardization and Measurement for Nanotechnology, National Center for Nanoscience and Technology, Beijing, 100190 (China); Xu, Jianxun; He, Meng [CAS Key Laboratory of Standardization and Measurement for Nanotechnology, National Center for Nanoscience and Technology, Beijing, 100190 (China); Song, Lexin [Department of Chemistry, University of Science and Technology of China, Hefei, 230026 (China); Chen, Dongliang, E-mail: chendl@mail.buct.edu.cn [College of Mechanical and Electrical Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Guo, Guangsheng, E-mail: guogs@bjut.edu.cn [Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, Key Laboratory of Advanced Functional Materials, Education Ministry of China, and Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124 (China); Dai, Hongxing, E-mail: hxdai@bjut.edu.cn [Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, Key Laboratory of Advanced Functional Materials, Education Ministry of China, and Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124 (China)

2016-09-15

X-ray Photoelectron Spectroscopy (XPS) is a useful surface sensitive tool to explore the particulate matter with different particle sizes. In this work, we report the analysis of elemental species in particulate matter with size ranging from 100 nm to 10 μm during the autumn haze of 2014 in Beijing. The size dependence of element composition and chemical state distribution on the particle surface was investigated. It was found that the number of investigated element species decreased from 8 (at stage 2) to 4 (at stage 10) with the decrease of particle sizes down to 100 nm, which is in accordance with the result from Transmission electron microscopy (TEM/EDX) observations. Three chemical states of nitrogen, the amide group (399.9 eV), the ammonium group (401.6 eV), and the nitrate group (407.2 eV), were confirmed according to the different binding energies. Nitrate was the main composition on the coarse particles, while the percentage of amide and ammonium at stage 3 (13.9% and 10.8% respectively) increased on the fine particles at stage 9 (46.8% and 38.8% respectively). The relative ratio of sulfate and ammonium (calculated 1:1) in the fine particles suggests that there is no enough NH{sub 4}{sup +} to neutralize the sulfuric acid and the surface of the PM is acidic. The result is useful to investigate the generation processes and the sources of collected particles. - Highlights: • The element composition of particles from 100 nm to 10 μm in haze was discussed • The chemical state was dominated by the particle size • The surface of PM was acidity • XPS was shown a useful tool in the aerosol research.

40 CFR 721.5350 - Substituted nitrile (generic name).

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Substituted nitrile (generic name... Substances § 721.5350 Substituted nitrile (generic name). (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted nitrile (PMN P-83...

Tuning electronic properties in graphene quantum dots by chemical functionalization: Density functional theory calculations

Science.gov (United States)

Abdelsalam, Hazem; Elhaes, Hanan; Ibrahim, Medhat A.

2018-03-01

The energy gap and dipole moment of chemically functionalized graphene quantum dots are investigated by density functional theory. The energy gap can be tuned through edge passivation by different elements or groups. Edge passivation by oxygen considerably decreases the energy gap in hexagonal nanodots. Edge states in triangular quantum dots can also be manipulated by passivation with fluorine. The dipole moment depends on: (a) shape and edge termination of the quantum dot, (b) attached group, and (c) position to which the groups are attached. Depending on the position of attached groups, the total dipole can be increased, decreased, or eliminated.

Semantic Web Compatible Names and Descriptions for Organisms

Science.gov (United States)

Wang, H.; Wilson, N.; McGuinness, D. L.

2012-12-01

Modern scientific names are critical for understanding the biological literature and provide a valuable way to understand evolutionary relationships. To validly publish a name, a description is required to separate the described group of organisms from those described by other names at the same level of the taxonomic hierarchy. The frequent revision of descriptions due to new evolutionary evidence has lead to situations where a single given scientific name may over time have multiple descriptions associated with it and a given published description may apply to multiple scientific names. Because of these many-to-many relationships between scientific names and descriptions, the usage of scientific names as a proxy for descriptions is inevitably ambiguous. Another issue lies in the fact that the precise application of scientific names often requires careful microscopic work, or increasingly, genetic sequencing, as scientific names are focused on the evolutionary relatedness between and within named groups such as species, genera, families, etc. This is problematic to many audiences, especially field biologists, who often do not have access to the instruments and tools required to make identifications on a microscopic or genetic basis. To better connect scientific names to descriptions and find a more convenient way to support computer assisted identification, we proposed the Semantic Vernacular System, a novel naming system that creates named, machine-interpretable descriptions for groups of organisms, and is compatible with the Semantic Web. Unlike the evolutionary relationship based scientific naming system, it emphasizes the observable features of organisms. By independently naming the descriptions composed of sets of observational features, as well as maintaining connections to scientific names, it preserves the observational data used to identify organisms. The system is designed to support a peer-review mechanism for creating new names, and uses a controlled

Chemical fractionation of radionuclides and stable elements in aquatic plants of the Yenisei River.

Science.gov (United States)

Bolsunovsky, Alexander

2011-09-01

The Yenisei River is contaminated with artificial radionuclides released by one of the Russian nuclear plants. The aquatic plants growing in the radioactively contaminated parts of the river contain artificial radionuclides. The aim of the study was to investigate accumulation of artificial radionuclides and stable elements by submerged plants of the Yenisei River and estimate the strength of their binding to plant biomass by using a new sequential extraction scheme. The aquatic plants sampled were: Potamogeton lucens, Fontinalis antipyretica, and Batrachium kauffmanii. Gamma-spectrometric analysis of the samples of aquatic plants has revealed more than 20 radionuclides. We also investigated the chemical fractionation of radionuclides and stable elements in the biomass and rated radionuclides and stable elements based on their distribution in biomass. The greatest number of radionuclides strongly bound to biomass cell structures was found for Potamogeton lucens and the smallest for Batrachium kauffmanii. For Fontinalis antipyretica, the number of distribution patterns that were similar for both radioactive isotopes and their stable counterparts was greater than for the other studied species. The transuranic elements (239)Np and (241)Am were found in the intracellular fraction of the biomass, and this suggested their active accumulation by the plants.

Search for chemical separations of the element 106 homologues in HF and HF-HCl media

International Nuclear Information System (INIS)

Trubert, D.; Monroy-Guzman, F.; Hussonnois, M.; Brillard, L.; Le Naour, C.; Constantinescu, O.

1996-01-01

In order to study the chemical properties of element 263 106 in aqueous media, fast, efficient and reproducible chromatographic separations were tested on its assumed homologous: Mo, W and U. Corroborative static and dynamic off-line experiments have shown that after fixation of these three elements on anion-exchange resin in HF medium, selective elution could be achieved by using suitable concentration of HCl - HF and HCl solutions. Separations of short-lived W isotopes, produced through heavy ion irradiation were also performed on-line. (author). 27 refs., 14 figs

PIXE - a new method for elemental analysis

International Nuclear Information System (INIS)

Johansson, S.A.E.

1983-01-01

With elemental analysis we mean the determination of which chemical elements are present in a sample and of their concentration. This is an old and important problem in chemistry. The earliest methods were purely chemical and many such methods are still used. However, various methods based on physical principles have gradually become more and more important. One such method is neutron activation. When the sample is bombarded with neutrons it becomes radioactive and the various radioactive isotopes produced can be identified by the radiation they emit. From the measured intensity of the radiation one can calculate how much of a certain element that is present in the sample. Another possibility is to study the light emitted when the sample is excited in various ways. A spectroscopic investigation of the light can identify the chemical elements and allows also a determination of their concentration in the sample. In the same way, if a sample can be brought to emit X-rays, this radiation is also characteristic for the elements present and can be used to determine the elemental concentration. One such X-ray method which has been developed recently is PIXE. The name is an acronym for Particle Induced X-ray Emission and indicates the principle of the method. Particles in this context means heavy, charged particles such as protons and a-particles of rather high energy. Hence, in PIXE-analysis the sample is irradiated in the beam of an accelerator and the emitted X-rays are studied. (author)

Chemistry of the heaviest elements

International Nuclear Information System (INIS)

Schaedel, M.

1992-08-01

The experimentally known chemical properties of elements 103,104, and 105, and the experimental techniques to obtain these properties on a one-atom- at-a-time base, are summarized. The chemical properties are compared with the lighter group 3,4 and 5 homologs and with the expected behaviour as obtained from theoretical calculations. In this transition region from the last actinide element to the beginning of the transactinide series one may expect to find evidence for increasingly strong relativistic effects altering the chemical behaviour. (orig.)

Determination of trace elements in tea by wavelength dispersive X-ray fluorescence spectroscopy

International Nuclear Information System (INIS)

Gong Chunhui; Zeng Guoqiang; Ge Liangquan; Li Jun; Wen Ziqiang

2013-01-01

Background: Measuring trace elements in tea can determine its nutritional value, verify the authenticity and place of origin, and detect the poisonous and harmful elements remaining in tea due to the application of chemical fertilizers and pesticides. Purpose: In order to reduce the time for sample preparation and the costs of equipment maintenance, wavelength dispersive X-ray fluorescence (WDXRF) spectroscopy was used to determine the trace elements in tea which is rapid, non-destructive and accurate. The contents of more than 20 elements can be measured simultaneously. Methods: Sample pieces were made by the sample preparation method of boric acid rebasing. To avoid the exogenous environmental pollution subjected in the growth of tea, we removed the residual dust of the tea by cleaning it. According to the principle that the standard samples should be similar types with the samples to be analyzed to select standard samples. The curves were built by SuperQ, which contained compiling the measurement conditions, establishing the measurement conditions, checking the angles, determining the measurement times, checking PHD and adding the contents and the names of sample pieces. The accuracy of the method can be obtained by comparing the measured values with the trace element contents of standard samples. The contents of trace elements in tea determined by WDXRF can be used to classify the tea attribution and the tea species through cluster analysis of SPSS software. Results: (1) The results show that the biggest relative standard deviation is 0.43% of Pb, and the precision is very good. (2) Five kinds of tea are taken separately in Fujian and Yunnan, measured three times with the established working curves. And tree diagram of cluster analysis can be obtained with SPSS software to analyze the measured average values with cluster analysis, coupling method between groups and Minkowski distance measurement techniques. It can be seen that in the tree diagram, when the

Introduction to the Chemical Management System

International Nuclear Information System (INIS)

Sawyer, J.G.

1993-01-01

The CMS, a Laboratory-wide electronic chemical inventory tracking system, will assist PNL by establishing comprehensive, integrated, Laboratory-wide databases supported by consistent and standardized procedures for chemical inventory management. It will provide PNL with the information needed to meet its current chemical management responsibilities and regulatory requirements. Its objectives are to provide an inventory of all chemicals being held at PNL facilities, to provide a specific location for all chemical containers, to ensure that health and safety regulatory codes are being upheld, and to provide PNL staff and managers with hazardous-chemical information for better inventory management. It is composed of 5 modules: chemical purchasing; chemical inventory; chemical names, properties, and hazardous groups; reporting; and system manager

Replacement names and nomenclatural comments for problematic species-group names in Europe's Neogene freshwater Gastropoda. Part 2

Directory of Open Access Journals (Sweden)

Thomas Neubauer

2014-07-01

Full Text Available In the course of a new database project on Miocene to Recent freshwater gastropods of Europe, a great many of primary and secondary homonyms were revealed. Such nomenclatural issues need clarification in order to avoid misunderstandings and wrong statements about geographical distributions and temporal ranges. The following 16 new names are introduced to replace existing homonyms: Theodoxus militaris jurisicpolsakae nom. n., Viviparus stevanovici nom. n., Melanopsis haueri ripanjensis nom. n., Melanopsis wolfgangfischeri nom. n., Micromelania ramacanensis nom. n., Pseudamnicola welterschultesi nom. n., Muellerpalia haszprunari nom. n., Muellerpalia pseudovalvatoides nom. n., Lithoglyphus gozhiki nom. n., Valvata heidemariae willmanni nom. n., Radix macaleti nom. n., Gyraulus okrugljakensis nom. n., Gyraulus rasseri nom. n., Gyraulus vrapceanus nom. n., Planorbarius halavatsi nom. n., and Segmentina mosbachensis nom. n. Additionally, six cases of homonyms are discussed that are not replaced by new names, because they are considered junior synonyms.

Geophagy practices and the content of chemical elements in the soil eaten by pregnant women in artisanal and small scale gold mining communities in Tanzania.

Science.gov (United States)

Nyanza, Elias C; Joseph, Mary; Premji, Shahirose S; Thomas, Deborah Sk; Mannion, Cynthia

2014-04-15

Geophagy, a form of pica, is the deliberate consumption of soil and is relatively common across Sub-Saharan Africa. In Tanzania, pregnant women commonly eat soil sticks sold in the market (pemba), soil from walls of houses, termite mounds, and ground soil (kichuguu). The present study examined geophagy practices of pregnant women in a gold mining area of Geita District in northwestern Tanzania, and also examined the potential for exposure to chemical elements by testing soil samples. We conducted a cross sectional study using a convenience sample of 340 pregnant women, ranging in age from 15-49 years, who attended six government antenatal clinics in the Geita District, Tanzania. Structured interviews were conducted in June-August, 2012, to understand geophagy practices. In addition, soil samples taken from sources identified by pregnant women practicing geophagy were analysed for mineral element content. Geophagy was reported by 155 (45.6%) pregnant women with 85 (54.8%) initiating the practice in the first trimester. A total of 101 (65%) pregnant women reported eating soil 2 to 3 times per day while 20 (13%) ate soil more than 3 times per day. Of 155 pregnant women 107 (69%) bought pemba from local shops, while 48 (31%) consumed ground soil kichuguu. The estimated mean quantity of soil consumed from pemba was 62.5 grams/day. Arsenic, chromium, copper, iron, manganese, nickel and zinc levels were found in both pemba and kichuguu samples. Cadmium and mercury were found only in the kichuguu samples. Based on daily intake estimates, arsenic, copper and manganese for kichuguu and copper and manganese for pemba samples exceed the oral Minimum Risk Levels designated by the U.S. Agency for Toxic Substance and Disease Registry. Almost 50% of participants practiced geophagy in Geita District consistent with other reports from Africa. Both pemba and kichuguu contained chemical elements at varying concentration, mostly above MRLs. As such, pregnant women who eat soil in Geita

The effect of pre-eclampsia-like syndrome induced by L-NAME on learning and memory and hippocampal glucocorticoid receptor expression: A rat model.

Science.gov (United States)

Zhu, Hao; Zhu, Weimin; Hu, Rong; Wang, Huijun; Ma, Duan; Li, Xiaotian

2017-02-01

We aimed to study the impacts of pre-eclampsia on the cognitive and learning capabilities of adolescent rat offspring and to explore the possible underlying mechanisms at the molecular level. Pregnant rats were subcutaneously injected with saline solution (control) (n = 16) or NG-nitro-L-arginine methyl ester (L-NAME) (n = 16) from the 13th day of gestation until parturition. The brain tissues from fetal rats delivered by cesarean section were examined in both groups with hematoxylin and eosin (H&E) staining. Rats born vaginally in both groups were subjected to the Morris water maze test when 8-week-old and their hippocampi were analyzed for glucocorticoid receptor (GR) expression. A pre-eclampsia-like model was successfully built in pregnant rats by infusion of the NO synthase inhibitor L-NAME, including phenotypes as maternal hypertension and proteinuria, high stillbirth rate, and fetal growth retardation. Neuroepithelial cell proliferation was found in the hippocampus of fetal rats in the L-NAME group. Grown to 8-week-old, the L-NAME group showed significantly longer escape latency than the control group in the beginning as well as in the end of navigation trials. At the same time, the swimming distance achieved by the L-NAME group was significantly longer than that of the control group. Such differences in cognitive and learning capabilities between the two groups were not gender dependent. Besides, the 8-week-old rats in the L-NAME group had increased GR expression in the hippocampus than the control group. Pre-eclampsia would impair cognitive and learning capabilities in adolescent offspring, and the upregulated expression of hippocampal GR may be involved in the underlying mechanisms.

Chemical profile of size-fractionated soils collected in a semiarid industrial area of Argentina

Science.gov (United States)

Morales Del Mastro, Anabella; Pereyra, Marcelo; Londonio, Agustín; Pereyra, Victoria; Rebagliati, Raúl Jiménez; Dawidowski, Laura; Gómez, Darío; Smichowski, Patricia

2014-12-01

A study was undertaken to assess the chemical profile of soil collected in Bahía Blanca (Argentina). In this industrial city, semiarid soils are affected by different industrial and agricultural activities, the presence of a saltpeter extraction facility, traffic and increasing urbanization. Sixteen soil samples (superficial and sub-superficial) were collected. Samples were sieved in two fractions (A plasma optical emission spectrometry (ICP OES). Anions (Cl-, F-, SO42-) and cations (K+, Na+ and NH4+) were determined by high performance liquid chromatography (HPLC) after an aqueous extraction. As expected, crustal elements namely, Al, Ca, Fe, Mg and Ti exhibited the highest concentrations. Mean elemental concentration ranged from Na+ ≅ SO42- > K+ > NO3-. Three indicators, namely, (i) coefficient of variation, (ii) coefficient of divergence and (iii) ratio of elemental concentration with respect to Ca were used to assess chemical, spatial and inter-profile variability. Chloride > Ca > Na+ > Mo > SO42-, dominated the variability indicating that these are key chemical markers for future assessment of crustal contribution to airborne particles in the area. The ratios Xi/Ca allowed discriminating the soil of the semi-arid region surrounding Bahía Blanca. The chemical profiles obtained in this study, particularly those of topsoil, will be a key input to characterize soil resuspension and its contribution to airborne particulate matter in a forthcoming receptor model analysis.

Closing in on chemical bonds by opening up relativity theory.

Science.gov (United States)

Whitney, Cynthia K

2008-03-01

This paper develops a connection between the phenomenology of chemical bonding and the theory of relativity. Empirical correlations between electron numbers in atoms and chemical bond stabilities in molecules are first reviewed and extended. Quantitative chemical bond strengths are then related to ionization potentials in elements. Striking patterns in ionization potentials are revealed when the data are viewed in an element-independent way, where element-specific details are removed via an appropriate scaling law. The scale factor involved is not explained by quantum mechanics; it is revealed only when one goes back further, to the development of Einstein's special relativity theory.

Multielement determination and speciation of major-to-ultratrace elements in green tea leaves by ICP-AES and ICP-MS

International Nuclear Information System (INIS)

Matsuura, Hirotaka; Hokura, Akiko; Haraguchi, Hiroki

2000-01-01

In order to investigate the multi-elemental composition of green tea leaves as well as chemical species in tea infusions, inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) were used for elemental analysis and elemental speciation with the aid of size exclusion chromatography (SEC). As a result, the multielement determination of major-to-ultratrace elements in green tea leaves and green tea infusions was carried out by ICP-AES and ICP-MS. About 40 elements in these tea samples could be determined in a wide concentration range of over 8 orders of magnitude. The extraction efficiency of each element was estimated as the ratio of its concentration in tea infusion to that in tea leaves. It was found from the experimental results that the elements in tea leaves could be classified into three characteristic groups, depending on their extraction efficiencies. Furthermore, tea infusions were analyzed by a combined system of SEC, UV absorption detector, and ICP-AES (or ICP-MS) for the speciation of major-to-ultratrace elements. Most of the elements in tea infusions were found to be present as associated complexes with large organic molecules. (author)

Chemical elements contamination of snow cover in region of coal production 'Karazhyra'

International Nuclear Information System (INIS)

Evlampieva, E.P.; Panin, M.S.

2008-01-01

Peculiarities of space distribution of chemical elements in hardphase and water-soluble falls of snow cover in region of coal deposit 'Karazhyra' are investigated. The maximal, minimal and background areas of elements accumulation in the snow of this region and distribution of their cumulative rates are determined. The main pollutants of snow cover unto background level are revealed.

Lexical Retrieval is not by Competition: Evidence from the Blocked Naming Paradigm

Science.gov (United States)

Navarrete, Eduardo; Del Prato, Paul; Peressotti, Francesca; Mahon, Bradford Z.

2014-01-01

A central issue in research on speech production is whether or not the retrieval of words from the mental lexicon is a competitive process. An important experimental paradigm to study the dynamics of lexical retrieval is the blocked naming paradigm, in which participants name pictures of objects that are grouped by semantic category (‘homogenous’ or ‘related’ blocks) or not grouped by semantic category (‘heterogeneous’ or ‘unrelated’ blocks). Typically, pictures are repeated multiple times (or cycles) within both related and unrelated blocks. It is known that participants are slower in related than in unrelated blocks when the data are collapsed over all within-block repetitions. This semantic interference effect, as observed in the blocked naming task, is the strongest empirical evidence for the hypothesis of lexical selection by competition. Here we show, contrary to the accepted view, that the default polarity of semantic context effects in the blocked naming paradigm is facilitation, rather than interference. In a series of experiments we find that interference arises only when items repeat within a block, and only because of that repetition: What looks to be ‘semantic interference’ in the blocked naming paradigm is actually less repetition priming in related compared to unrelated blocks. These data undermine the theory of lexical selection by competition and indicate a model in which the most highly activated word is retrieved, regardless of the activation levels of nontarget words. We conclude that the theory of lexical selection by competition, and by extension the important psycholinguistic models based on that assumption, are no longer viable, and frame a new way to approach the question of how words are retrieved in spoken language production. PMID:25284954

Elemental analyses of bulk and individual particles by PIXE and SEM-EDX

International Nuclear Information System (INIS)

Kasahara, Mikio; Shinoda, Kazuyuki; Takahashi, Kanji; Yoshida, Kouji.

1993-01-01

The atmospheric aerosol samples were collected by a stacked filter method under the various environmental conditions. The elemental concentrations of aerosol particles were measured using PIXE analysis as a bulk sample. And also elemental compositions of about 200 individual particles per each sample were measured by SEM-EDX analysis. In this study, the correspondencies of analytical results measured by both analyses as well as chemical characteristics of individual and bulk aerosols were investigated. (author)