scholarly journals Geochemical characteristics of Triassic and Cretaceous phosphorite horizons from the Transdanubian Mountain Range (western Hungary): genetic implications

2018 ◽  
Vol 82 (S1) ◽  
pp. S147-S171 ◽  
Author(s):  
Zsuzsa Molnár ◽  
Gabriella B. Kiss ◽  
István Dunkl ◽  
György Czuppon ◽  
Federica Zaccarini ◽  
...  

ABSTRACTThe carbonate-dominated Mesozoic sequence of the Transdanubian Mountain Range contains Triassic, uranium-enriched phosphorite layers and Cretaceous, REE-enriched nodular phosphorite. Detailed investigation of these deposits may have an economic benefit because of their large U and REE contents. The dominant minerals in the Triassic phosphorite are carbonate-bearing fluorapatite (CFA) and calcite. According to the electron-probe microanalysis (EPMA) the U is mainly associated with the CFA crystals. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) measurement shows that CFA contains 137–612 ppm U and 113–261 ppm total REE + Y. The LA-ICP-MS U-Pb age of the uppermost phosphorite horizon is 237 ± 11 Ma, which conforms with the stratigraphic age of the host limestone.The Cretaceous nodular phosphorite occurs on the base of an Aptian crinoid-bearing limestone mostly in the form of encrustations around bio- and silicic-clasts, but the clasts also contain phosphorite. The main minerals in these crusts are CFA, calcite, quartz, glauconite and Fe-oxide-hydroxides. Based on EPMA the REE enrichment is related to CFA and LA-ICP-MS measurements show that it contains 748–2953 ppm total REE + Y.The redox-sensitive proxies and the shape of NASC normalized REE patterns indicate that both phosphorites formed in anoxic environments. There are significant differences between these deposits such as appearance, rock-forming minerals, and U and REE contents which indicate differences in their sedimentary environments. The present results suggest that the Triassic phosphorite was formed by inorganic precipitation in a reducing environment close to sea-mounts. The Cretaceous occurrence resulted from a concentric growth mechanism in cold, ascending seawater at the continental margin environment during the anoxic Selli Event (OAE 1a) and/or Paquier Episode (OAE 1b). The critical raw material contents were derived from other sources.

Minerals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 236
Author(s):  
Evangelos Tzamos ◽  
Platon N. Gamaletsos ◽  
Giovanni Grieco ◽  
Micol Bussolesi ◽  
Anthimos Xenidis ◽  
...  

Antimony is a common metalloid occurring in the form of Sb-sulfides and sulfosalts, in various base and noble metal deposits. It is also present in corresponding metallurgical products (concentrates) and, although antimony has been considered a penalty element in the past, recently it has gained interest due to its classification as a critical raw material (CRM) by the European Union (EU). In the frame of the present paper, representative ore samples from the main Sb-bearing deposits of Greece (Kilkis prefecture, Chalkidiki prefecture (Kassandra Mines), and Chios Isl.) have been investigated. According to optical microscopy and electron probe microanalysis (EPMA) data, the Greek ores contain stibnite (Sb2S3), boulangerite (Pb5Sb4S11), bournonite (PbCuSbS3), bertherite (FeSbS4), and valentinite (Sb2O3). Bulk analyses by inductively coupled plasma mass spectrometry (ICP-MS) confirmed, for the first time published, the presence of a significant Hg content in the Kilkis Sb-ore. Furthermore, Kassandra Mines ores are found to contain remarkable amounts of Bi, As, Sn, Tl, and Se (excluding Ag, which is a bonus element). The above findings could contribute to potential future exploration and exploitation of Sb ores in Greece.


2019 ◽  
Author(s):  
Ingo Strenge ◽  
Carsten Engelhard

<p>The article demonstrates the importance of using a suitable approach to compensate for dead time relate count losses (a certain measurement artefact) whenever short, but potentially strong transient signals are to be analysed using inductively coupled plasma mass spectrometry (ICP-MS). Findings strongly support the theory that inadequate time resolution, and therefore insufficient compensation for these count losses, is one of the main reasons for size underestimation observed when analysing inorganic nanoparticles using ICP-MS, a topic still controversially discussed.</p>


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