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Atomic Emission Spectrometry (atomic + emission_spectrometry)
Kinds of Atomic Emission Spectrometry Selected AbstractsBIOREMEDIATIVE POTENTIAL OF CHROMULINA FREIBURGENSIS IN CULTURE FROM THE BERKELEY PITJOURNAL OF PHYCOLOGY, Issue 2001Article first published online: 24 SEP 200 Dakel, S. M.1 & Mitman, G. G.2 1Department of Environmental Engineering; 2Department of Biological Sciences, Montana Tech of The University of Montana, Butte, MT 59701 USA The Berkeley Pit, part of the largest Superfund site in the United States, is an open-pit copper mine that operated from 1955 through 1982. Today, the Berkeley Pit contains approximately 1200 billion liters of metal laden water with an average pH of 2.7, and 12 grams/liter of dissolved solids. The principle dissolved ions include aluminum, arsenic, calcium, cadmium, copper, iron, potassium, magnesium, manganese, sulfates, and zinc. A species from Division Chrysophyta,Chromulina freiburgensis Dofl. was isolated from this extreme environment. This species has been tested in the laboratory through a series of controlled experiments to determine bioremediative potential. Optimal temperature was determined by monitoring growth with cell counts at temperatures ranging from 5°C to 40°C . The optimal nutrient ratio was determined by varying nitrogen (NaNO3) and phosphorus (Na2HPO4) levels. An experimental matrix varying nutrients was developed to test for bioremediative potential which included: initial and final pH measurements; initial and final Ion Chromatography Pairing,Atomic Emission Spectrometry (ICP-AES) for dissolved metals; and examination of final samples under Transmission Electron Microscopy (TEM). From these experiments, Chromulina freiburgensis was found to grow optimally in Berkeley Pit surface water with cell densities reaching ten million cells per milliliter at 10°C with additions of 50 mg NaNO3/L and 5 mg Na2HPO4/L. This large biomass was also found to increase diversity and abundance of heterotrophs. At the optimal nutrient level, this species was found to increase pH from 2.21 to 2.47 over 90 days. Significant removal of calcium, iron, nickel, and silica was observed. [source] Flux growth of La-doped lead zirconate stannate titanate antiferroelectric crystalsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 10 2008Lin Wang Abstract Relaxor antiferroelectric single crystals lead lanthanum zirconate stannate titanate (PLZST) with the composition around the morphotropic phase boundary (MPB) have been grown by flux method using 50 wt% PbO-PbF2 -B2O3 as a flux. The obtained crystals are light yellow in color. The XRD patterns revealed that the habitual faces of the obtained crystal are (001). The crystal morphology was studied and related to a layer growth mechanism controlled by two-dimensional growth. The chemical composition of as-grown crystal was analyzed by inductively coupled plasma atomic emission spectrometry (ICP), indicating a slight decrease of the amount of Ti compared to the starting materials. The result was verified by the XRD patterns with the phase transformation from the co-existence of tetragonal and rhombohedra phases to the single tetragonal phase. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Arsenic, lead, and other trace elements in soils contaminated with pesticide residues at the Hanford site (USA)ENVIRONMENTAL TOXICOLOGY, Issue 2 2003Jerry Yokel Abstract The primary purpose of this study was to characterize arsenic (As) and lead (Pb) concentrations in former orchard soils contaminated with lead arsenate pesticides at the Hanford site in Washington state (USA). Surface samples (n = 31) were collected from former orchard soils (in cultivation during the pre-Hanford period) at five locations at the 100 Areas and at one location at the Old Hanford Townsite (OHT). Another set of samples (n = 17) was collected over a soil depth interval of 10,50 cm at the four locations with the highest As and Pb surface concentrations. All samples were analyzed for 22 trace elements (including As and Pb) with inductively coupled plasma,atomic emission spectrometry (ICP,AES). The mean, standard deviation, and range for As in the surface soils were 30, 61, and 2.9,270 mg/kg dry wt, respectively. The corresponding statistics for Pb were 220, 460, and 6.5,1900 mg/kg dry wt, respectively. As and Pb concentrations in the surface soils were positively and significantly correlated (r = 0.91, Bonferroni p < 0.05). Descriptive statistics and bivariate correlations were also computed for other trace elements. As and Pb mean concentrations in the surface soils each differed significantly (p < 0.05) among Hanford locations, with the highest concentrations at the 100-H and 100-F Areas. Although both As and Pb mean concentrations decreased with soil depth, regression and correlation coefficients only, for Pb significantly differed from zero (b = ,0.0372, r = ,0.805, Bonferroni p < 0.05). Compared with data in the literature As and Pb concentrations found in this study exceeded background levels but were typical of orchard soils. Furthermore, mean As and Pb soil concentrations were in the range of various toxicological benchmarks derived for protection of human and ecological receptors. © 2003 Wiley Periodicals, Inc. Environ Toxicol 18: 104,114, 2003 [source] Multiple Functionalization of Mesoporous Silica in One-Pot: Direct Synthesis of Aluminum-Containing Plugged SBA-15 from Aqueous Nitrate Solutions,ADVANCED FUNCTIONAL MATERIALS, Issue 1 2008Y. Wu Abstract Aluminum-containing plugged mesoporous silica has been successfully prepared in an aqueous solution that contains triblock copolymer templates, nitrates, and silica sources but without using mineral acid. The acidity of the solution can be finely tuned from pH 1.4 to 2.8 according to the amount of the introduced aluminum species which ranged from an Al/Si molar ratio of 0.25/1 to 4.0/1. The aluminum nitrate additive in the starting mixture, along with the weak acidity produced by the nitrates, contributes to the formation of plugged hexagonal structures and the introduction of different amounts of aluminum species into the mesostructure. Characterization by X-ray diffraction, transmission electron microscopy, and N2 sorption measurements show that the Al-containing plugged silicas possess well-ordered hexagonal mesostructures with high surface areas (700,860 m2,g,1), large pore volume (0.77,1.05 cm3,g,1) and, more importantly, combined micropores and/or small mesopores in the cylindrical channels. Inductively coupled plasma,atomic emission spectrometry results show that 0.7,3.0 wt,% aluminum can be introduced into the final samples. 27Al MAS NMR results display that about 43,60% aluminum species are incorporated into the skeleton of the Al-containing silicas and the amount of the framework aluminum increases as the initial added nitrates rises. Scanning electron microscopy images reveal that the directly synthesized Al-containing plugged silica has a similar morphology to that of traditional SBA-15. Furthermore, the Al-containing plugged samples have excellent performances in the adsorption and the catalytic decomposition of isopropyl alcohol and nitrosamine. Finally, the direct synthesis method is used to produce plugged mesoporous silicas that contain other metals such as chromium and copper, and the resultant samples also show good catalytic activities. [source] Effects of hydrological processes on the chemical composition of riverine suspended sediment in the Zhujiang River, ChinaHYDROLOGICAL PROCESSES, Issue 12 2003Quanzhou Gao Abstract The chemical composition of riverine suspended sediment is the integration of the weathering crust minerals, soil organic matter and erosion agency within a specific drainage basin, which has been largely disturbed by the human activities. Selected metal elements of the riverine suspended sediment in the Zhujiang River were analysed using inductively coupled plasma,atomic emission spectrometry (ICP,AES) in three different hydrological phases from 1997 to 1998 at Makou and Sanshui hydrographic gauge stations, located at the lower reaches of the two main tributaries of the Zhujiang River, i.e. the Xijiang and the Beijing Rivers respectively. Organic carbon and nitrogen were also analysed using a conventional element analyser. The results demonstrate that the chemical composition of the riverine suspended sediment show obvious variability in different hydrological phases, which closely correlate to the organic matter content in suspended sediment. Intensified erosion in the flood phase results in lower concentration of the organic matter than that in the lower water level phase. The riverine suspended sediment with rich organic matter in the lower water level phase adsorbs some metal elements from the river water. Copyright © 2003 John Wiley & Sons, Ltd. [source] Comparison of some properties on the different types of pestil: a traditional product in TurkeyINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 8 2005Ozlem Cagindi Summary Pestil is a traditional dried fruit snack, which is consumed in Turkey. Wheat starch is mixed with different clarified fruit juices such as grape, mulberry, apricot or plum and cooked using traditional techniques. In this work the proximate chemical composition (moisture, ash, fat, crude protein and total carbohydrate), energy value and thickness of grape, apricot and mulberry pestils were investigated. The colour properties (Hunter L, a and b) were determined by a Minolta Chroma-Meter and the mineral content (Ca, Fe, K, Mg, Na, Cu, Zn, Mn) of each product was determined by inductively coupled plasma atomic emission spectrometry (ICP-AES). The carbohydrate value of pestil samples ranged between 73.7 and 82.4% and energy value was between 321.5 and 356.4 kcal 100 g,1. Mulberry pestil was a better source of energy than grape and apricot pestils. Apricot pestils were rich in calcium, sodium and zinc, and mulberry pestil samples were rich in magnesium. [source] Ion imprinted polymer particles for separation of yttrium from selected lanthanidesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 9 2006Ramakrishnan Kala Abstract Lanthanide(III) (Dy, Gd, Tb and Y) ion imprinted polymer (IIP) materials were synthesized via single pot reaction by mixing lanthanide imprint ion with 5,7-dichloroquinoline-8-ol, 4-vinylpyridine, styrene, divinylbenzene and 2,2,-azobisisobutyronitrile in 2-methoxyethanol porogen. The imprint ion was removed by stirring the above materials (after powdering) with 6 mol/L HCl to obtain the respective lanthanide IIP particles. Y-Dy, Y-Gd and Dy-Gd polymer particles were obtained by physically mixing equal amounts of the respective leached individual lanthanide(III) particles. Control polymer (CP) particles were similarly prepared without imprint ion. Application of the above synthesized polymer particles was tested for separation of Y from Dy, Gd and Tb employing batch and column SPE methods using inductively coupled plasma atomic emission spectrometry for the determination. Optimization studies show that Y present in 500 mL can be preconcentrated using Dy-Gd IIP particles and eluted with 20 mL of 1.0 mol/L of HCl, providing an enrichment factor of , 25. Dy-Gd IIP particles offer higher selectivity coefficients for Y over other lanthanides compared to other IIP particles and commercial liquid,liquid extractants. Selectivity studies for Y over other coexisting inorganic species (other than lanthanides) were also conducted and the results obtained show a quantitative separation of Y from other inorganics other than Cu(II) and Fe(III). Furthermore, both batch and column studies indicate the purification of yttrium concentrate from 55.0 ± 0.2 to 65.2 ± 0.2% in a single stage of operation. [source] Differentiation of eight tea (Camellia sinensis) cultivars in China by elemental fingerprint of their leavesJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 14 2009Yingxu Chen Abstract BACKGROUND: Tea is an infusion made from dried leaves of tea (Camellia sinensis) and can be a good dietary source of essential trace metals for humans. Therefore, it is necessary to consider variations in element content of tea leaves among tea cultivars. Thus, elemental fingerprint techniques, based on elemental contents (Al, B, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, P, Pb, and Zn) determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) and multivariate statistical analysis, have been used to differentiate eight tea cultivars. RESULTS: The ranges of element concentrations in leaves of the eight cultivars were in good agreement with those obtained in previous studies and the level of most elements in tea leaves was significantly different among cultivars. The classifications of eight tea cultivars were 100% accurate in total by principal component analysis (PCA), hierarchical cluster analysis (HCA), linear discriminant analysis (LDA), and back-propagation neural network (BPNN) analysis. CONCLUSION: Each cultivar presented a distinctive element fingerprint and the elements in tea leaves can be significant predictors in differentiating tea cultivars. Copyright © 2009 Society of Chemical Industry [source] Volatile organoselenium monitoring in production and gastric digestion processes of selenized yeast by solid-phase microextraction-multicapillary gas chromatography coupled microwave-induced plasma atomic emission spectrometry,APPLIED ORGANOMETALLIC CHEMISTRY, Issue 12 2004J. Sanz Landaluze Abstract Evolution of volatile organoselenium compounds in the production and gastric digestion of selenized yeast has been monitored. The industrial production of these kinds of material, employed as food supplements, has been simulated in a process of yeast enrichment with inorganic selenium selenium (IV) in different growth media, with variation of the pH value. The in vitro gastric digestion process was carried out with pepsin in an acid and salt mixture. Determination of volatile species of selenium was achieved coupling solid-phase microextraction (SPME) for preconcentration and sample,matrix separation and microwave-induced plasma atomic emission spectrometry, in combination with multicapillary (MC) gas chromatography for separation and detection of the selenium species. The MC column was operated at low temperatures (,30 °C). The method was optimized, using a chemometric approach, with respect to the detection of organoselenium species such as dimethylselenide, diethylselenide and dimethyldiselenide. SPME sampling was carried out in the headspace above the corresponding solutions. Separation is fast, with a chromatogram being obtained in less than 5 min, and the detection limits were at the low parts per billion level for all species investigated. The results of the yeast enrichment process demonstrate inorganic selenium transformation into volatile organic species. The presence of inorganic selenium gave rise to at least five different volatile species after metabolization by yeast, with dimethylselenide and dimethyldiselenide being the predominant species. Commercial pasteurized yeast, containing mainly selenomethionine for use as a food supplement, and tablets were found to be still active under conditions of the simulation of the digestion process, even though producing relatively low amounts of organoselenium compounds. Copyright © 2004 John Wiley & Sons, Ltd. [source] Nutrients apparent digestibility coefficients of selected protein sources for juvenile Siberian sturgeon (Acipenser baerii Brandt), compared by two chromic oxide analyses methodsAQUACULTURE NUTRITION, Issue 6 2009H. LIU Abstract Apparent digestibility coefficients (ADCs) of dry matter (ADCd), crude protein (ADCp), energy (ADCe) and amino acids in selected feedstuffs were determined for juvenile Siberian sturgeon (8.38 ± 0.20 g). The tested feedstuffs were fishmeal (FM), meat and bone meal (MBM), poultry by-product meal, hydrolysed feather meal, fermented feather meal solvent-extracted cottonseed meal and soybean meal. ADCs were determined using a reference diet and test diets at 7 : 3 ratios with 5 g kg,1 chromic oxide (Cr2O3) as an inert marker. Fish were reared in a recirculating system and fed to apparent satiation five times daily. Cr2O3 in diets and faeces samples were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) and acid-digestion colorimetry (AC) methods, respectively. The results showed that ICP-AES method was more accurate for Cr2O3 determination than AC method, and the results determined by ICP-AES method were used in this study. ADCd and ADCp of seven tested ingredients were lowest for MBM (59.1 and 84.5%) and highest for FM (79.9 and 94.5%); ADCe of tested ingredients were from 71.8% for SECM to 93.2% for FM. ADCs of amino acid in test ingredients followed similar trend to the ADCp. The ADCs of individual amino acids varied from 61.6% (histidine in MBM) to 98.8% (valine in FM). [source] Comparison of Artificial Neural Networks with Partial Least Squares Regression for Simultaneous Determinations by ICP-AESCHINESE JOURNAL OF CHEMISTRY, Issue 11 2007Mohamad KHAYATZADEH MAHANI Abstract Simultaneous determination of several elements (U, Ta, Mn, Zr and W) with inductively coupled plasma atomic emission spectrometry (ICP-AES) in the presence of spectral interference was performed using chemometrics methods. True comparison between artificial neural network (ANN) and partial least squares regression (PLS) for simultaneous determination in different degrees of overlap was investigated. The emission spectra were recorded at uranium analytical line (263.553 nm) with a 0.06 nm spectral window by ICP-AES. Principal component analysis was applied to data and scores on 5 dominant principal components were subjected to ANN. A 5-5-5 (input, hidden and output neurons) network was used with linear transfer function after both hidden and output layers. The PLS model was trained with five latent variables and 20 samples in calibration set. The relative errors of predictions (REP) in test set were 3.75% and 3.56% for ANN and PLS respectively. [source] Underpotential Deposition Study and Determination of Bismuth on Gold Electrode by Using VoltammetryCHINESE JOURNAL OF CHEMISTRY, Issue 6 2002Yong-Ling Du Abstract The cyclic voltammetry (CV) and the semidifferential anodic stripping voltammetry (SdASV) were used for investigation of bismuth(III) underpotential deposition (UPD) on gold electrode. Based on the excellent electrochemical properties of Au/ Bi UPD system, a new method for determining bismuth (III) was established. A solution of 0.1 mol/L HNO3 was selected as the supporting electrolyte. Factors affecting the Bi(III) UPD and stripping steps were investigated and an optimized analytical procedure was developed. The calibration plots for Bi(III) concentration in the range 1.25 × 10,8 -1.0 × 10,7 mol/L were obtained. The detection limit, calculated as three times the standard deviation of the analytical signal of 8.3 × 10,8 mol/L for a 90 s electrodeposition at 0.00 V (while the solution magnetically stirred at a speed of 300 rpm), was 7.5 × 10,9 mol/ L. For 8 successive determinations of 1.25 × 10,7 mol/L Bi(III), the obtained RSD (relative standard deviation) was 0.4%. The developed method was applied to bismuth determining in medicine and urine samples. The analytical results were compared with that of atomic emission spectrometry (AES) method. [source] | |||||||||||||