scholarly journals Development of a Kriging Assessment Framework and Impact Pathway for Researching Contamination With Potentially Toxic Elements in Urban Landfill Soil

2021 ◽  
Author(s):  
Azizi Abu Bakar ◽  
Minoru Yoneda ◽  
Noor Zalina Mahmood
Keyword(s):  
Ordinary Kriging ◽  
Inductively Coupled Plasma ◽  
Explanatory Variable ◽  
Cost Effective ◽  
Explanatory Variables ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms ◽  
Regression Error ◽  
Impact Pathway

Abstract Landfill post-closure with contaminant concentration in soil below permissible limit assessed at limited spot does not represent the contamination issue. Assessment limit to professionals also does not gives a potential of change to practice constant assessment to a wider context of assessor - citizen living nearby - as a collaborative effort to sustain a safe environment. Therefore sizeable, qualitative, and cost-effective analysis of the concentrations of contaminants is needed and this work recommends kriging assessment and the logical impact pathway framework as factors of change in landfill aftercare management. The kriging framework is developed utilising lead (Pb) and chromium (Cr) data from inductively coupled plasma mass spectrometry (ICP-MS) analysis. The development of the kriging framework is conducted based on the observation of censored data from ICP-MS analysis. The estimation analysis involves the analysis of ordinary kriging with regression analysis, showing the interpolation of spatial correlation and regression error. Hence, ordinary kriging with regression of the variable of interest, i.e., Pb, using the data of the explanatory variable, i.e., Cr, is inappropriate. Further investigation with the utilisation of guess-field kriging analysis hypothetically exposed a potential contaminated area using an existing but limited number of explanatory variables; although, guess-field kriging may possibly result immense uncertainty at the area where the explanatory variable does not exist. Besides, this work anticipated outcomes in societal impact and sustainability practices from the proposed kriging framework by recommending a logical impact pathway. The development of the kriging framework and impact pathway reassure the necessary actions to be executed by responsible parties and act as the stimulus of a wider spectrum of improvement initiatives to oversee real issues, such as the time of occurrence, and to prevent negative impacts on the environment and humans.

scholarly journals Germanium determination in environmental object by the method of mass spectrometry with inductively coupled plasma

2019 ◽  
Vol 85 (4) ◽  
pp. 110-113
Author(s):  
Olexandr Ponomarenko ◽  
Anatolyi Samchuk ◽  
Kateryna Vovk ◽  
Igor Shvaika ◽  
Ganna Grodzinskaya
Keyword(s):  
Mass Spectrometry ◽  
Sample Preparation ◽  
Inductively Coupled Plasma ◽  
Microwave Field ◽  
Antitumor Effects ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms ◽  
Relative Standard

The analytical technologies of sample preparation of rocks and mushrooms using the microwave field for the determination of germanium by the method of mass spectrometry with inductively coupled plasma (ICP-MS analysis) have been developed. Germanium is a rare element. Germanium is homology of silicon and carbon. To date, the definition of low content of germanium in geological objects is a rather complex analytical task, which requires its concentration - extraction, co-precipitation, ion exchange. At present, the harmonious combination of the method of natural objects decomposition in the microwave field and germanium determination using ICP-MS analysis is particularly promising. Sample preparation of silicate rocks for ICP-MS determination of germanium was carried out by decomposition in a mixture of hydrofluoric, phosphate and nitric acids (5: 5: 2) in a microwave oven program at 240°C for 30 min. Sample preparation of mushrooms for ICP-MS germanium determination was carried out according to the following scheme. Initially, the dried sample was sealed in the presence of CaO, after dissolving it in a mixture of HNO3+HF+H3PO4 (6:6:1). Ge solution was extracted by Nazarenko V.A. extraction method. The developed analytical schemes have made it possible to significantly reduce the duration and labor intensity of sample preparation. The obtained solutions were analyzed using an inductively coupled plasma mass spectrometer. The developed method for determining germanium by ICP-MS analysis has been successfully tested on standard rock samples. The obtained results are in accordance with the accepted attribute, the relative standard deviation Sr ranges from 0.7-0.9. The data on the content and distribution of germanium in the Boletales fungi are obtained. They indicate wild mushrooms contain high levels of germanium, especially Boletus and Mushroom biospores. These studies are necessary because the essential properties of germanium and its compounds attract special attention of scientists today. Complementary Ge compounds which have hypotensive, bactericidal, antiviral and antitumor effects have already been synthesized.

scholarly journals Gold Partitioning in a Model Multiphase Mineral-Hydrothermal Fluid System: Distribution Coefficients, Speciation and Segregation

Minerals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 890 ◽  
Author(s):  
Sergey Lipko ◽  
Vladimir Tauson ◽  
Valeriy Bychinskii
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluid Phase ◽  
Distribution Coefficients ◽  
Crystal Defects ◽  
Geothermal Systems ◽  
Fluid System ◽  
Experimental Conditions ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms

The characteristics of Au partitioning in a multiphase, multicomponent hydrothermal system at 450 °C and 1 kbar pressure were obtained using experimental and computational physicochemical modelling and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis. Sphalerite and magnetite contained 0.1–0.16 ± 0.02 µg/g Au and coexisted with galena and bornite which contained up to 73 ± 5 and 42 ± 10 µg/g Au, respectively. Bornite and chalcopyrite were the most effective Au scavengers with cocrystallization coefficients Au/Fe and Au/Cu in mineral-fluid system n–n × 10−2. Sphalerite and magnetite were the weakest Au absorbers, although Fe impurity in sphalerite facilitated Au uptake. Using the phase composition correlation principle, Au solubility in minerals was estimated (µg/g Au): low-Fe sphalerite = 0.7, high-Fe sphalerite = 5, magnetite = 1, pyrite = 3, pyrite-Mn = 7, pyrite-Cu = 10, pyrrhotite = 21, chalcopyrite = 110, bornite = 140 and galena = 240. The sequence reflected increasing metallicity of chemical bonds. Gold segregation occurred at crystal defects, and on surfaces, and influenced Au distribution due to its segregation at crystal interblock boundaries enriched in Cu-containing submicron phases. The LA-ICP-MS analysis of bulk and surficial gold admixtures revealed elevated Au content in surficial crystal layers, especially for bornite and galena, indicating the presence of a superficial nonautonomous phase (NAP) and dualism in the distribution of gold. Thermodynamic calculations showed that changes in experimental conditions, primarily in sulfur regime, increased the content of the main gold species (AuCl2− and AuHS0) and decreased the content of FeCl20, the prevailing form of iron in the fluid phase. The elevation of S2 and H2S fugacity affected Au partitioning and cocrystallization coefficients. Using Au content in pyrite, chalcopyrite, magnetite and bornite from volcanic-sedimentary, skarn-hosted and magmatic-hydrothermal sulfide deposits, the ranges of metal ratios in fluids were estimated: Au/Fe = n × 10−4−n × 10−7 and Au/Cu = n × 10−4−n × 10−6. Pyrite and magnetite were crystallized from solutions enriched in Au compared to chalcopyrite and bornite. The presence of NAP, and associated dualism in distribution coefficients, strongly influenced Au partitioning, but this effect does not fully explain the high gold fractionation into mineral precipitates in low-temperature geothermal systems.

Evaluation of Painted Pottery from the Mesa Verde Region Using Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS)

2002 ◽  
Vol 67 (1) ◽  
pp. 137-144 ◽  
Author(s):  
Robert J. Speakman ◽  
Hector Neff
Keyword(s):  
Mass Spectrometry ◽  
Laser Ablation ◽  
Inductively Coupled Plasma ◽  
Cost Effective ◽  
American Southwest ◽  
Inductively Coupled ◽  
Mesa Verde ◽  
Icp Ms ◽  
Plasma Mass Spectrometry ◽  
Mesa Verde Region

For decades archaeologists have struggled with the problem of accurately determining organic and mineral-based paints in pottery from the American Southwest. Using Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS), we have developed a simple and cost-effective method that permits classification of painted surfaces into mineral and organic-based categories. By applying this method to Mesa Verde and Mancos Black-on-white pottery from the Mesa Verde Region, we were able to distinguish easily between mineral and organic-based paints. Preliminary data also suggest that multiple sub-groups of mineral-based paints exist within these ceramic types, indicating that multiple recipes for manufacturing paint may have been employed by prehistoric potters from this region.

Aerosol extraction and direct laser ablation ICP-MS analysis of the fine and ultrafine fractions of regolith

2019 ◽  
Vol 20 (3) ◽  
pp. 280-298
Author(s):  
Paul A. Morris ◽  
Alex Christ ◽  
Edward J. Mikucki
Keyword(s):  
Mass Spectrometry ◽  
Laser Ablation ◽  
Inductively Coupled Plasma ◽  
Content Type ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms ◽  
Direct Laser ◽  
Plasma Mass Spectrometry ◽  
Supplementary Material

The <10, <4, <2.5 and <1 µm fractions of eight regolith samples have been extracted as aerosols, then analysed for more than 60 elements by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Precision and accuracy rivals that of conventional digestion and ICP-MS analysis for most elements, but the aerosol extraction and ablation approach can be completed within 30 min, avoids compromising the sample by screening, column settling, fusion and/or digestion, and includes data for elements such as Br, Cl, I and Se that are conventionally analysed by individual procedures. Major element chemistry and scanning electron microscope (SEM) imagery show that the aerosol fractions of regolith are dominated by kaolinite, with quartz in aeolian regolith. The aerosol fractions of Si- and Ca-rich regolith have higher trace element concentrations than the coarser fraction (0.45–2 mm), but chalcophile elements are depleted in the aerosols of Fe-rich regolith relative to the coarser fraction. Improvements in in-field analytical technology coupled with aerosol extraction mean that fine and ultrafine fraction chemistry can be used to guide mineral exploration programmes in close to real time.Supplementary material: The results of the laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis of filter papers are available at https://doi.org/10.6084/m9.figshare.c.4562807

scholarly journals Development of an In-Field Method for the Detection of Barium in Various Water Samples Using Differential Pulse Anodic Stripping Voltammetry

2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
S. Ridgway ◽  
M. Wajrak
Keyword(s):  
Inductively Coupled Plasma ◽  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Cost Effective ◽  
Differential Pulse ◽  
Field Method ◽  
Barium Concentration ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Anodic Stripping

This work presents a reliable, cost-effective, rapid and in-field voltammetric method for the detection of barium. The optimized method consists of an ultrathin mercury film deposited in situ on a glassy carbon electrode in dilute potassium chloride without deoxygenation, using differential pulse anodic stripping voltammetry (DP-ASV). Application of the method allowed for the quantitative determination of barium concentration in a variety of waters and brake pad dust samples. Comparative analysis of sample results from DP-ASV with inductively coupled plasma mass spectroscopy (ICP-MS) showed a mean percent difference of 1.8%.

scholarly journals Multi-elemental analysis of high-purity molybdenum by electrothermal vaporization inductively coupled plasma mass spectrometry

2020 ◽  
Author(s):  
N.S. Medvedev ◽  
A.V. Volzhenin ◽  
A.I. Saprykin
Keyword(s):  
Mass Spectrometry ◽  
Trace Elements ◽  
High Purity ◽  
Inductively Coupled Plasma ◽  
Radiation Detectors ◽  
Double Beta Decay ◽  
Electrothermal Vaporization ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms

High purity molybdenum and its compounds are used for the synthesis of ionizing radiation detectors for search for dark matter and double beta decay. Properties of these detectors largely depend on their trace composition. The new mass-spectrometry with inductively coupled plasma (ICP-MS) and electrothermal vaporization (ETV) method was developed for the analysis of high-purity molybdenum. The samples were introduced into the ICP using the ETV device. The vaporization curves of matrix element (molybdenum) and trace elements were studied in detail. The dependence of analytical signal and limits of detection (LODs) of analytes versus ETV-ICP-MS instrumental parameters (ICP power, transport flow, ion optics settings) was established. The proposed method of ETV-ICP-MS analysis allowed us to control the content of 28 trace elements in high-purity molybdenum with a purity of 6N (99.9999% wt.) and provided LODs from 0.3 to 200 ng g-1. Using of ETV for ICP-MS analysis of molybdenum led to decreasing of the LODs of trace elements from 3 to 200 times comparing with ICP-MS analysis with standard sample introduction system. The validation of proposed ETV-ICP-MS method was performed by spike experiment and by comparing the results of ETV-ICP-MS, ICP-MS, and atomic absorption spectrometry with electrothermal vaporization (GFAAS) analysis.

scholarly journals Characterization of Four Copper Materials for Application as Reference Materials for High Precision Copper Isotope Analysis by Laser Ablation Inductively Coupled Plasma Multi-Collector Mass Spectrometry

2021 ◽  
Vol 9 ◽  
Author(s):  
Zhaoping Yang ◽  
Simon Edward Jackson ◽  
Thomas Skulski
Keyword(s):  
Normal Distribution ◽  
Reference Materials ◽  
Inductively Coupled Plasma ◽  
Inductively Coupled ◽  
Ms Analysis ◽  
Icp Ms ◽  
The Mean ◽  
Isotope Measurements ◽  
Cu Isotope

Laser ablation inductively coupled plasma multi-collector mass spectrometry (LA-MC-ICP-MS) allows rapid, in situ, highly precise measurements of Cu isotope ratios of native Cu and Cu-bearing minerals. However, the National Institute of Standards and Technology Cu-metal isotope standard NIST SRM976 that is commonly used to calibrate LA-MC-ICP-MS Cu isotope measurements of native Cu is no longer available. We have investigated the suitability of four Cu metal materials, SSC-1, SSC-3 and SSC-4 (cathode Cu metal rods) and CUPD-1 (Cu anode sawings), originally developed by the Canada Centre for Mineral and Energy Technology (CANMET) as certified reference materials for trace element analysis, as Cu isotope reference materials for LA-MC-ICP-MS analysis and solution nebulization (SN) of Cu. The Cu isotopic composition and homogeneity of these four materials were characterised by SN- and LA-MC-ICP-MS, and are reported for the first time. The bulk Cu isotopic compositions, expressed as δ65CuSRM976 in per mil (‰) relative to NIST SRM976 with combined uncertainties (U, k = 2), of SSC-1, SSC-3 and SSC-4, determined utilizing SN-MC-ICP-MS, are identical within analytical uncertainty at 0.03 ± 0.07‰ (n = 29), 0.04 ± 0.04‰ (n = 28), and 0.05 ± 0.08‰ (n = 29), respectively; the composition of CUPD-1 is 2.14 ± 0.08‰ (n = 28). The compositions are 0.01 ± 0.07‰ (n = 29), 0.04 ± 0.06‰ (n = 29), 0.03 ± 0.06‰ (n = 28) and 2.15 ± 0.06‰ (n = 28), respectively, relative to the European Reference Material ERM®-AE633 Cu isotope standard. The Cu isotope homogeneity of the four new reference materials was assessed by determining whether multiple individual in situ Cu isotope measurements made by LA-MC-ICP-MS analysis (43 µm spot size), using each of the other three reference materials as a calibrator, approximate a single normal distribution. We also investigate whether there are statistically significant differences between the mean δ65Cu values of three independent data sets for each of the Cu isotope reference materials using one-way analysis of variance (ANOVA). Normality tests (graphical assessment of normal distribution quantile-quantile plots, and the Shapiro-Wilk, Jarque-Bera and reduced chi-squared statistic tests) show that: 1) the Cu isotope data acquired on SSC-1, SSC-3, SSC-4 and CUPD-1 do not depart significantly from a normal distribution, 2) the scatter of the Cu isotope data is due to analytical uncertainty with 95% confidence, and 3) there are no other significant sources of scatter; e.g. heterogeneity of the reference materials. The results of one-way ANOVA reveal that the mean difference of the δ65Cu value for each of the reference materials SSC-1, SSC-3, SSC-4 and CUPD-1 is statistically not significant at the 0.05 level. The mean δ65CuSRM976 values with combined uncertainties (U, k = 2) of SSC-1, SSC-3, SSC-4 and CUPD-1, determined by LA-MC-ICP-MS using each of the other three reference materials as a calibration standard, are 0.03 ± 0.09‰ (n = 132), 0.05 ± 0.09‰ (n = 154), 0.03 ± 0.09‰ (n = 144) and 2.14 ± 0.10‰ (n = 106), respectively. These values are in agreement with those determined by SN-MC-ICP-MS analysis at the 95% confidence level and have excellent precision (2 s.d. ≤ 0.10‰). These results suggest that SSC-1, SSC-3, SSC-4 and CUPD-1 can be considered isotopically homogeneous at a spatial resolution of 43 μm, and they are suitable reference materials for calibration and quality control of in situ and solution nebulization Cu isotope analyses of Cu.

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