scholarly journals Post-Depositional Alteration of Calcium Carbonate Phases in Archaeological Ceramics: Depletion and Redistribution Effects

Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 749
Author(s):  
William D. Gilstrap ◽  
Jennifer L. Meanwell ◽  
Elizabeth H. Paris ◽  
Roberto López Bravo ◽  
Peter M. Day
Keyword(s):  
Inductively Coupled Plasma ◽  
Bulk Composition ◽  
Optical Emission ◽  
Depositional Environments ◽  
Emission Spectrometry ◽  
Archaeological Ceramics ◽  
Inductively Coupled ◽  
Prehistoric Pottery ◽  
Plasma Mass Spectrometry ◽  
History Of

The final stage in the life history of prehistoric pottery prior to archaeological recovery is usually the longest, and frequently the most dynamic. The remains of archaeological ceramics spend hundreds to thousands of years deposited within the upper layers of the earth’s crust where they encounter the same diagenetic environmental processes as the surrounding natural materials. Harsh conditions of subterranean environments induce physical stresses and chemical reactions, causing alterations of ceramic structure and composition. This is especially true of carbonate-rich ceramics, as carbonate phases are soluble when deposited within acidic environments. This paper examines common carbonate depletion and accretion effects of post-depositional environments on ancient ceramics from two rather different geological and archaeological contexts: Mesoamerica and the Mediterranean. Potters in both regions produce vessels with carbonate-rich materials—clays, calcite, limestone—that alter due to long exposure to low-pH sediments and continual water table fluctuations. Ceramic petrography is employed to identify traces of carbonate alterations within ceramic microstructure and to characterize fabrics. Elemental compositions of the same sherds are characterized through either scanning electron microscopy coupled with energy-dispersive spectrometry (SEM-EDS), inductively coupled plasma mass spectrometry and optical emission spectrometry (ICP-MS/OES) or neutron activation analysis (NAA). This method enabled comparison of the differing effects of post-depositional alteration of carbonate phases on bulk composition signatures commonly used to determine provenance.

Geochemistry of major, trace and rare earth elements in coals from the Tazareh mine, eastern Alborz coalfield, NE Iran

2020 ◽  
Vol 20 (3) ◽  
pp. 381-398
Author(s):  
Afieh Tatar ◽  
Masood Alipour-Asll
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Inductively Coupled Plasma ◽  
Hanging Wall ◽  
Optical Emission ◽  
Emission Spectrometry ◽  
Humid Climate ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry ◽  
Host Rocks

The Tazareh mine in the eastern Alborz coalfield is one of the most important coal-producing areas in Iran and contains medium volatile (19.1–31.5%), low sulfur (0.015–0.491%) and variable ash yield (3–31.5%) bituminous coal. In this research, a total of 21 samples were collected from the Tazareh coal layers, footwall and hanging wall. The concentrations of rare earth elements (REEs) and other elements were determined by inductively coupled-plasma mass spectrometry (ICP-MS) and inductively coupled plasma-optical emission spectrometry (ICP-OES). Additionally, traditional features of coal and host rocks were studied by X-ray diffraction (XRD) and petrographic methods. The concentration coefficient (CC) of Tazareh coal samples show that Sc (CC = 2.71), Be (CC = 2.68) and Ni (CC = 2.30) are slightly enriched, Li, Cr, Pb, Sb, V, Cs, As, Co, Cu, Nb, Y, Rb, Tl, REE, Zr, Zn, Ta and Th (0.5 < CC < 2) are normal, and concentrations of remaining trace elements are lower than the average world hard coals. The NASC-normalized REEs pattern and (La/Yb)n, (La/Sm)n, (Gd/Yb)n, and (La/Lu)n ratios in the Tazareh coal confirm that the LREEs are enriched relative to HREEs, and comparatively, the degree of LREE enrichment of coal is lower than that of coal-bearing shale and argillaceous shale. Coal-bearing strata were deposited under oxic conditions in a warm-humid climate. The average content of REE + Y in Tazareh coal (58 ppm) is lower than world coals (83 ppm), while Sc is enriched.

scholarly journals P2O5-Free Cerium Containing Glasses: Bioactivity and Cytocompatibility Evaluation

Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3267
Author(s):  
Gigliola Lusvardi ◽  
Francesca Sgarbi Stabellini ◽  
Roberta Salvatori
Keyword(s):  
Inductively Coupled Plasma ◽  
Optical Emission ◽  
Emission Spectrometry ◽  
X Ray Diffraction ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Doped Glasses ◽  
Plasma Mass Spectrometry ◽  
Sbf Solution ◽  
Xrd Techniques

(1) Background: valuation of the bioactivity and cytocompatibility of P2O5-free and CeO2 doped glasses. (2) Methods: all glasses are based on the Kokubo (K) composition and prepared by a melting method. Doped glassed, K1.2, K3.6 and K5.3 contain 1.2, 3.6, and 5.3 mol% of CeO2. Bioactivity and cytotoxicity tests were carried out in simulated body fluid (SBF) solution and murine osteocyte (MLO-Y4) cell lines, respectively. Leaching of ions concentration in SBF was determined by inductively coupled plasma mass spectrometry (ICP-MS) and optical emission spectrometry (ICP-OES). The surface of the glasses were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. (3) Results: P2O5-free cerium doped glasses are proactive according to European directives. Cerium increases durability and retards, but does not inhibit, (Ca10(PO4)6(OH)2, HA) formation at higher cerium amounts (K3.6 and K5.3); however, cell proliferation increases with the amount of cerium especially evident for K5.3. (4) Conclusions: These results enforce the use of P2O5-free cerium doped bioactive glasses as a new class of biomaterials.

Advantages, drawbacks and applications of mixed Ar–N2 sources in inductively coupled plasma-based techniques: an overview

2014 ◽  
Vol 6 (16) ◽  
pp. 6170-6182 ◽  
Author(s):  
G. L. Scheffler ◽  
D. Pozebon
Keyword(s):  
Mass Spectrometry ◽  
Inductively Coupled Plasma ◽  
Optical Emission ◽  
Emission Spectrometry ◽  
Icp Oes ◽  
Mixed Gas ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Plasma Mass Spectrometry ◽  
Plasma Optical Emission Spectrometry

This review deals with mixed gas Ar–N2 plasmas, highlighting advantages, limitations and applications of them in inductively coupled plasma optical emission spectrometry (ICP OES), inductively coupled plasma mass spectrometry (ICP-MS) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) techniques, covering publications in the last three decades.

scholarly journals Multi-element analysis of Macedonian wines by inductively coupled plasma–mass spectrometry (ICP–MS) and inductively coupled plasma–optical emission spectrometry (IP–OES) for regional classification

2013 ◽  
Vol 32 (1) ◽  
pp. 265 ◽  
Author(s):  
Violeta Ivanova-Petropulos ◽  
Helmar Wiltsche ◽  
Trajče Stafilov ◽  
Marina Stefova ◽  
Herber Motter ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Inductively Coupled Plasma ◽  
Accurate Determination ◽  
Optical Emission ◽  
Optical Emission Spectrometry ◽  
Emission Spectrometry ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Plasma Mass Spectrometry ◽  
Plasma Optical Emission Spectrometry

Major, minor, and trace elements in wines from the Republic of Macedonia were determined in this study. Both inductively coupled plasma–mass spectrometry (ICP-MS) and inductively coupled plasma– optical emission spectrometry (ICP-OES) were used for accurate determination of the concentration of 42 elements (Ag, Al, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Ho, La, Lu, Mg, Mn, Mo, Na, Nd, Ni, P, Pb, Pr, S, Sm, Tb, Ti, Tl, Tm, U, V, Yb, Zn, Zr) in 25 Macedonian white, rose, and red wines from different wine regions. By means of factor and cluster analyses, the wines were discriminated according to wine type (white vs. red) and geographical origin. The main discriminant elements were B, Ba, Ca, Fe, Mg, Mn, P, and S. 

scholarly journals The effect of collecting area on the element content of Hungarian acacia honeys

2018 ◽  
pp. 129-138
Author(s):  
Nikolett Czipa ◽  
Andrea Kántor ◽  
Loránd Alexa ◽  
Béla Kovács
Keyword(s):  
Inductively Coupled Plasma ◽  
Geographical Origin ◽  
Optical Emission ◽  
Emission Spectrometry ◽  
Linear Discriminant ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Plasma Mass Spectrometry ◽  
Plasma Optical Emission Spectrometry ◽  
One Way Anova

Six macroelements and twelve microelements were identified in thirty-six Hungarian acacia honeys collected from ten counties by inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS). One-Way ANOVA (LSD and Dunnett T3 test) and linear discriminant analysis (LDA) were used to determine the statistically verified differences among the honey samples with different geographical origin. Significant differences were established among the samples from different counties in Na, P, S, Fe, Ni, Cu and Sr concentrations. Based on the macroelement content of honeys, the separation of samples with different geographical origin was not successful because the percent of correctly categorised cases was only 64.9%. However, examining the As, B, Ba, Cu, Fe Mn, Ni and Sr concentration, the separation of different groups was convincing since the percent of correctly classified cases was 97.2%. Thus, the examination of microelement concentration may be able to determine the geographical origin of acacia honeys.

scholarly journals An overview of methods used for quantification of heavy metal contents in vegetal samples

2021 ◽  
Vol 3 (2) ◽  
pp. 7-15
Author(s):  
Gina Vasile Scaeteanu ◽  
◽  
Rodica Maria Majdar ◽  
Andrei Mot ◽  
Keyword(s):  
Heavy Metals ◽  
Inductively Coupled Plasma ◽  
Anodic Stripping Voltammetry ◽  
Accurate Determination ◽  
Optical Emission ◽  
Stripping Voltammetry ◽  
Absorption Spectrometry ◽  
Emission Spectrometry ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry

Continuous monitoring of heavy metals content in vegetal products is a priority for food control and a risk assessment strategy for human health. Having in view the importance of heavy metals surveillance, the aim of this paper is to identify, on the basis of literature data, the most suitable procedures and techniques used for accurate determination of them in vegetal samples. In most cases, quantification of heavy metals in the vegetal matrix is preceded by digestion performed through different protocols chosen carefully because this is a critical step for obtaining accurate results. Among most used techniques for heavy metals’ assessment from vegetal products reported by literature it worth to be mentioned: atomic absorption spectrometry (AAS), inductively coupled plasma-mass spectrometry (ICP-MS), inductively coupled plasma - optical emission spectrometry (ICP-OES), X-ray fluorescence (XRF), neutron activation analysis (NAA), anodic stripping voltammetry (ASV).

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