scholarly journals Sequential extraction of carbonaceous siltstone rock for multi-element analysis by ICP OES

2018 ◽  
Vol 7 (2) ◽  
pp. 145-152 ◽  
Author(s):  
Medet Junussov ◽  
Ferenc Mádai ◽  
Bánhidi Olivér
Keyword(s):  
Sequential Extraction ◽  
Inductively Coupled Plasma ◽  
Mineralogical Composition ◽  
Water Soluble ◽  
Residual Fraction ◽  
Emission Spectrometry ◽  
Chemical Extraction ◽  
Element Analysis ◽  
X Ray

Abstract The carbonaceous siltstone rock material is a disseminated sulfide-rich sedimentary rock from a sediment-hosted gold deposit of Bakyrchik. The Bakyrchik deposit is located in Eastern Kazakhstan, which includes in Qalba gold province. The main purpose of this paper is a demonstration on chemical extraction of heavy metals from the carbonaceous siltstone rock and detection of its elemental concentrations. In the work was used a rock sample from the deposit which is a sericizited carbonaceous-siltstone rock. In sequential extraction method was selected four stages such as water soluble fraction (reaction with deionized water) for extraction of water soluble metals, reducible metal fraction (reaction with hydroxyl ammonium chloride) for extracting all reducible metals, organics and sulfides (reaction with hydrogen peroxide) for dissolution of organics and copper sulfide, and extraction of metal oxides and residual fraction (reaction with aqua regia) for extracting of all remaining metals. The paper comprises analytical methods for research outlooks. They are X-Ray Diffraction (determination of mineralogical composition), X-Ray Fluorescence (determination of chemical composition) and Inductively Coupled Plasma – Optical Emission Spectrometry (determination of heavy metal concentrations).

scholarly journals Geochemistry and Mineralogy of Ice-Dammed Lake Sediments of the Lębork Deposit

2021 ◽  
Author(s):  
Radosław Rogoziński ◽  
Alina Maciejewska
Keyword(s):  
Chemical Composition ◽  
Lake Sediments ◽  
Inductively Coupled Plasma ◽  
Mineralogical Composition ◽  
Raw Material ◽  
Element Analysis ◽  
X Ray ◽  
Dominant Component ◽  
Clay Deposits ◽  
Dammed Lake

AbstractVarved clay deposits from ice-dammed lakes are a particularly important and broadly applied raw material used for the production of high-quality ceramics (red bricks, roof tiles, etc.), but the mineralogy and geochemistry of these sediments are not fully understood. The aim of the present study was to determine the chemical and mineralogical composition of ice-dammed lake sediments of the Lębork deposit. Major-element analysis of the compositions of selected samples from the ice-dammed lake clays was performed by X-ray fluorescence (XRF) and trace elements were determined by inductively coupled plasma-mass spectrometry. The mineralogical composition of clay samples was determined by X-ray diffraction (XRD). Analyses of the chemical composition of the ice-dammed lake clays of the Lębork deposit showed that the dominant component was SiO2 with a mean content of 56.13 wt.%; the second most abundant component was Al2O3, with a mean content for the entire deposit of 11.61 wt.%. Analysis by ICP-MS indicated the presence of rare earth elements (REE), e.g. cerium, neodymium, lanthanum, and praseodymium; their mean contents are: 56.9, 27.0, 26.3, and 7.3 ppm, respectively. Mineralogical analysis of the varved clays identified quartz, muscovite, calcite, and clay minerals – illite, kaolinite, and montmorillonite. The material filling the Lębork basin is characterized by small lateral and vertical variability in chemical composition. The results of the present study may be of considerable importance in determining the parent igneous, metamorphic, and sedimentary rocks, the weathering products of which supplied material to the ice-dammed lake, as well as in determining the mechanisms and character of the sedimentation process itself.

Determination of Nitrogen, Phosphorus, and Potassium in Water-Soluble Fertilizers by Inductively Coupled Plasma Emission Spectrometry

1987 ◽  
Vol 70 (4) ◽  
pp. 760-761
Author(s):  
Danton D. Nygaard ◽  
John J. Sotera
Keyword(s):  
Inductively Coupled Plasma ◽  
Water Soluble ◽  
Emission Spectrometry ◽  
Inductively Coupled ◽  
Extension Tube ◽  
Plasma Emission Spectrometry ◽  
Phosphorus And Potassium ◽  
Icp Torch ◽  
Nitrogen Phosphorus

Abstract A modification of an inductively coupled plasma (ICP) emission spectrometer is described that enables the simultaneous determination of nitrogen, phosphorus, and potassium in water-soluble fertilizers. A quartz extension tube is added to the ICP torch to exclude air from the plasma, thus allowing accurate nitrogen determination without adversely affecting sensitivity for other analytes. The modification also requires an 18 mg/L argon coolant flow to protect the tube from the heat of the plasma. Detection limits are 20 mg/L for nitrogen and 50 μg/L for phosphorus and potassium. Three NBS reference salts and 2 commercially available fertilizers were analyzed by the method, and results are in excellent agreement with known values.

scholarly journals Determination of Phosphorus in Fertilizers by Inductively Coupled Plasma Atomic Emission Spectrometry

2002 ◽  
Vol 85 (6) ◽  
pp. 1241-1246 ◽  
Author(s):  
Wei Min Yang ◽  
Rhonda L Boles ◽  
Thomas P Mawhinney
Keyword(s):  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Water Soluble ◽  
Atomic Emission Spectrometry ◽  
Emission Spectrometry ◽  
Plasma Atomic Emission ◽  
Plasma Atomic Emission Spectrometry ◽  
Inductively Coupled ◽  
Phosphorus Determination

Abstract An inductively coupled plasma atomic emission spectrometry (ICP-AES) method was developed for the determination of phosphorus in fertilizers. Total phosphorus, direct extraction available phosphorus (EDTA), and water-soluble phosphorus, reported as phosphorus pentoxide (P2O5), in 15 Magruder check fertilizers were measured by ICP-AES, and the results were compared with those obtained by the AOAC official method. Five analytical wavelengths of phosphorus, 177.499, 178.287, 213.618, 214.914, and 253.565 nm, were tested for the determination of phosphorus in fertilizers, and their detection limits were obtained. Acid effects of perchloric acid and possible matrix effects of aluminum, calcium, magnesium, potassium, and sodium were negligible for phosphorus determination. Wavelength 213.618 nm was the best analytical wavelength for phosphorus determination by all 3 sample preparation methods for the selected Magruder fertilizers. The results demonstrated that the accuracy and precision of the ICP-AES method were comparable with those of the official methods.

scholarly journals Simplified ICP OES-Based Method for Determination of 12 Elements in Commercial Bottled Birch Saps: Validation and Bioaccessibility Study

Molecules ◽  
2020 ◽  
Vol 25 (5) ◽  
pp. 1256
Author(s):  
Maja Welna ◽  
Anna Szymczycha-Madeja ◽  
Pawel Pohl
Keyword(s):  
Inductively Coupled Plasma ◽  
Optical Emission ◽  
Direct Analysis ◽  
Emission Spectrometry ◽  
Dietary Intakes ◽  
Icp Oes ◽  
Element Analysis ◽  
Inductively Coupled

Commercially bottled birch saps (BSs) were analyzed for several nutrient (Ca, Cu, Fe, Mg, and Zn) and toxic (As, Cd, Ni, and Pb) elements using inductively coupled plasma optical emission spectrometry (ICP OES). The method was validated under the conditions of several sample preparation procedures, including a traditional digestion as well as alternative non-digestion schemes. It was found that the direct analysis of untreated BSs gives the best results, i.e., limits of detection at 0.02–5.8 ng mL−1, precision better than 5%, accuracy from 98.0% to 104.5% and determination of 12 elements in a short time (~1 min per sample). The multi-element analysis of nine commercially available bottled BSs showed that they contained mainly Mg and Ca, small quantities of Mn, Zn, Cu, and Fe, but are free from toxic elements such as As, Cd, Ni, and Pb. Additionally, the nutritional value of BSs was examined using in vitro gastro-intestinal digestion (GID) to determine the bioaccessible fraction of elements. Accordingly, bioaccessibility of nutritious ones (Ca, Cu, Fe, Mg, Zn) was <40%. Drinking daily 1 L of BSs covered <2.5% of recommended dietary intakes (RDIs) of the aforementioned elements. Only the bioaccessibility of Mn highly contributes to its RDI.

Determination of Heavy Metals and Their Speciation in Street Dusts by Inductively Coupled Plasma-Optical Emission Spectrometry after a Community Bureau of Reference Sequential Extraction Procedure

2013 ◽  
Vol 96 (4) ◽  
pp. 864-869 ◽  
Author(s):  
Huseyin Altundag ◽  
Mustafa Imamoglu ◽  
Secil Doganci ◽  
Erkan Baysal ◽  
Sinem Albayrak ◽  
...  
Keyword(s):  
Sequential Extraction ◽  
Inductively Coupled Plasma ◽  
Extraction Procedure ◽  
Optical Emission ◽  
Optical Emission Spectrometry ◽  
Sequential Extraction Procedure ◽  
Emission Spectrometry ◽  
Inductively Coupled ◽  
Plasma Optical Emission Spectrometry

Abstract Sequential selective extraction techniques are commonly used to fractionate the solid-phase forms of metals in soils. This procedure provides measurements of extractable metals from media, such as acetic acid (0.11 M), hydroxyl ammonium chloride (0.1 M), hydrogen peroxide (8.8 M) plus ammonium acetate (1 M), and aqua regia stages of the sequential extraction procedure. In this work, the extractable Pb, Cu, Mn, Sr, Ni, V, Fe, Zn, and Cr were evaluated in street dust samples from Sakarya, Turkey, between May and October 2009 using the three-step sequential extraction procedure described by the Community Bureau of Reference (BCR, now the Standards, Measurements, and Testing Programme) of the European Union. The sampling sites were divided into 10 categories; a total of 50 street dusts were analyzed. The determination of multielements in the samples was performed by inductively coupled plasma-optical emission spectrometry. Validation of the proposed method was performed using BCR 701 certified reference material. The results showed good agreement between the obtained and the certified values for the metals analyzed.

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