scholarly journals Apatite as a tracer for magmatic-hydrothermal ore-forming processes

2021 ◽  
Author(s):  
S. Karvinen ◽  
◽  
A. Heinonen ◽  
C. Beier
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Trace Element ◽  
Analytical Techniques ◽  
Layered Intrusions ◽  
Minor Phase ◽  
Trace Element Chemistry ◽  
Hydrothermal Processes ◽  
A Minor

This project focuses on the trace element chemistry of igneous apatite in various magmatic systems with the use of in situ analytical techniques. The composition of apatite may possibly be used as a tracer for various magmatic-hydrothermal processes due to the breadth of chemical substitutions possible within the structure. Apatite is found in many mineralized layered intrusions as a minor phase. Apatite may be utilized in the tracking of metasomatic fluids in layered intrusions or in geochronological studies in the absence of other commonly used phases i.e. zircon. Apatite accumulations can be exploited economically for phosphorus and possibly for rare earth elements as well.

Simultaneous determination of Sm–Nd isotopes, trace-element compositions and U–Pb ages of titanite using a laser-ablation split-stream technique with the addition of water vapor

2021 ◽  
Author(s):  
Le Zhang ◽  
Jia-Lin Wu ◽  
Yanqiang Zhang ◽  
Ya-Nan Yang ◽  
Pengli He ◽  
...  
Keyword(s):  
Rare Earth ◽  
Water Vapor ◽  
Laser Ablation ◽  
Rare Earth Elements ◽  
Trace Element ◽  
Simultaneous Determination ◽  
Nd Isotopes ◽  
Trace Element Contents

Titanite is a widespread accessory nesosilicate with high trace-element contents including rare-earth elements, Th, and U, and is thus suitable for in situ isotopic and trace-element analyses and U–Pb dating....

Minor and trace element chemistry of carbonates, apatites and magnetites in some African carbonatites

1996 ◽  
Vol 60 (400) ◽  
pp. 415-425 ◽  
Author(s):  
J. B. Dawson ◽  
I. M. Steele ◽  
J. V. Smith ◽  
M. L. Rivers
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Trace Element ◽  
Light Rare Earth ◽  
Trace Element Chemistry ◽  
Element Chemistry ◽  
Fe And Mn ◽  
Ppm Level ◽  
Light Rare Earth Elements ◽  
Cu And Zn

AbstractIn calcites and dolomites in seven African carbonatites, SrO, FeO and MnO occur in concentrations from 1 to 2 wt.%, whereas Ce, Y, Cu and Zn occur only at the ppm level. Sr, Ce and Y partition preferentially into calcite relative to co-existing dolomite, whereas Fe and Mn favour dolomite. Sr partitions preferentially into calcite relative to co-exisiting apatite, but the light rare-earth elements partition into apatite. Magnetite from Kerimasi contains up to 13 wt.% MgO and 6 wt.% MnO, extending the known ranges in composition of magnetites from carbonatites.

Synthetic zircon doped with hafnium and rare earth elements: A reference material for in situ hafnium isotope analysis

2011 ◽  
Vol 286 (1-2) ◽  
pp. 32-47 ◽  
Author(s):  
Christopher M. Fisher ◽  
John M. Hanchar ◽  
Scott D. Samson ◽  
Bruno Dhuime ◽  
Janne Blichert-Toft ◽  
...  
Keyword(s):  
Rare Earth ◽  
Reference Material ◽  
Rare Earth Elements ◽  
Isotope Analysis

scholarly journals Leaching of Rare Earth Elements from Central Appalachian Coal Seam Underclays

Minerals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 577
Author(s):  
Scott N. Montross ◽  
Jonathan Yang ◽  
James Britton ◽  
Mark McKoy ◽  
Circe Verba
Keyword(s):  
Rare Earth ◽  
Coal Seam ◽  
Rare Earth Elements ◽  
Chelating Agent ◽  
Analytical Techniques ◽  
Leach Solution ◽  
Alternative Source ◽  
Waste Products ◽  
Energy Applications ◽  
Sequential Digestion

Rare earth elements (REE) are necessary for advanced technological and energy applications. To support the emerging need, it is necessary to identify new domestic sources of REE and technologies to separate and recover saleable REE product in a safe and economical manner. Underclay rock associated with Central Appalachian coal seams and prevalent in coal utilization waste products is an alternative source of REE to hard rock ores that are mainly composed of highly refractory REE-bearing minerals. This study utilizes a suite of analytical techniques and benchtop leaching tests to characterize the properties and leachability of the coal seam underclays sampled. Laboratory bench-top and flow-through reactor leaching experiments were conducted on underclay rock powders to produce a pregnant leach solution (PLS) that has relatively low concentrations of gangue elements Al, Si, Fe, and Th and is amenable to further processing steps to recover and produce purified REE product. The leaching method described here uses a chelating agent, the citrate anion, to solubilize elements that are adsorbed, or weakly bonded to the surface of clay minerals or other mineral solid phases in the rock. The citrate PLS produced from leaching specific underclay powders contains relatively higher concentrations of REE and lower concentrations of gangue elements compared to PLS produced from sequential digestion using ammonium sulfate and mineral acids. Citrate solution leaching of underclay produces a PLS with lower concentrations of gangue elements and higher concentrations of REE than achieved with hydrochloric acid or sulfuric acid. The results provide a preliminary assessment of the types of REE-bearing minerals and potential leachability of coal seam underclays from the Central Appalachian basin.

scholarly journals Allanite Geochemical Response to Hydrothermal Alteration by Alkaline, Low-Temperature Fluids

Minerals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 392 ◽  
Author(s):  
Katarzyna Gros ◽  
Ewa Słaby ◽  
Petras Jokubauskas ◽  
Jiří Sláma ◽  
Gabriela Kozub-Budzyń
Keyword(s):  
Rare Earth ◽  
Low Temperature ◽  
Rare Earth Elements ◽  
Geochemical Evolution ◽  
Additional Component ◽  
Second Stage ◽  
Ce Anomaly ◽  
Hydrothermal Processes ◽  
Fluid Infiltration ◽  
Two Stages

Allanite is one of the main rare earth elements (REE)-rich accessory minerals in composite dykes from the granitoid pluton of Karkonosze. These dykes differ in composition from the bulk of the pluton by elevated rare earth elements (REE), Y, Zr, and alkali contents, suggesting contribution of an additional component. Allanite exhibits complex alteration textures, which can be divided into two stages. The first stage is represented by allanite mantles, formed by fluid infiltration into previously crystallized magmatic allanite. These zones have low totals, are Ca-, Al-, Mg-, and light REE (LREE)-depleted, and Y-, heavy REE (HREE)-, Th-, Ti-, and alkali-enriched. The fractionation between LREE and HREE was caused by different mobility of complexes formed by these elements in aqueous fluids. The second stage includes recrystallized LREE-poor, Y-HREE-rich allanite with variable Ca, Al, Mg, and REE-fluorocarbonates. The alteration products from both stages demonstrate higher Fe3+/(Fe2+ + Fe3+) ratios and a negative Ce anomaly. These features point to the alkaline, low-temperature, and oxidized nature of the fluids. The differences in mobility and solubility of respective ligands show that the fluids from the first stage may have been dominated by Cl, whereas those of the second stage may have been dominated by F and CO2 (and PO4 in case of one sample). The inferred chemistry of the fluids resembles the overall geochemical signature of the composite dykes, indicating a major contribution of the hydrothermal processes to their geochemical evolution.

Significance of the metasomatized lithospheric mantle in the formation of early basalts and Cu – platinum group element sulfide mineralization in the Coldwell Complex, Midcontinent Rift, Canada

2019 ◽  
Vol 56 (7) ◽  
pp. 693-714 ◽  
Author(s):  
David J. Good ◽  
Peter C. Lightfoot
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Trace Element ◽  
Lithospheric Mantle ◽  
Group Element ◽  
Light Rare Earth ◽  
Midcontinent Rift ◽  
Northern Margin ◽  
Lithospheric Mantle Source ◽  
Light Rare Earth Elements

A diverse suite of tholeiitic to alkaline basalt and gabbroic intrusions located in the Coldwell Complex on the northern margin of the Midcontinent Rift exhibit unusual trace element signatures that show enriched large ion lithophile elements and light rare earth elements with negative Nb and Zr anomalies. These features are not typical of magmas derived by partial melting within or above a rising mantle plume, as might be expected in an early Midcontinent Rift magmatic event. In this paper, we provide a detailed geochemical study of a 500 m thick sequence of metabasalt that represents the earliest stage of magmatism in the Coldwell Complex. We show that contamination or crystallization processes or subsequent metasomatism cannot explain the trace element variations. Instead, we propose partial melting in a metasomatized Subcontinental Lithospheric Mantle source to explain the decoupled behavior of large ion lithophile elements from light rare earth elements and heavy rare earth elements and rare earth elements from high field strength elements and the enriched Nd isotope signature of metabasalt. Similar features occur in unit 5b of the Mamainse Point Volcanic Group located at the northern margin of the Rift. An objective of this paper is to relate Two Duck Lake gabbro, host rock for low-sulfur, high precious metal sulfide mineralization at the Marathon deposit, to the metabasalt sequence. The excellent match of trace element abundances in Two Duck Lake gabbro to metabasalt unit 3 confirms an early Coldwell Complex age for metabasalt and a Subcontinental Lithospheric Mantle source for Cu – platinum group element mineralized gabbros.

Quantitative Cathodoluminescence Mapping with Application to a Kalgoorlie Scheelite

2009 ◽  
Vol 15 (3) ◽  
pp. 222-230 ◽  
Author(s):  
Colin M. MacRae ◽  
Nicholas C. Wilson ◽  
Joel Brugger
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Trace Element Level ◽  
Gaussian Peak ◽  
X Ray ◽  
Element Abundances ◽  
Inductively Coupled ◽  
Peak Fitting

AbstractA method for the analysis of cathodoluminescence spectra is described that enables quantitative trace-element-level distributions to be mapped within minerals and materials. Cathodoluminescence intensities for a number of rare earth elements are determined by Gaussian peak fitting, and these intensities show positive correlation with independently measured concentrations down to parts per million levels. The ability to quantify cathodoluminescence spectra provides a powerful tool to determine both trace element abundances and charge state, while major elemental levels can be determined using more traditional X-ray spectrometry. To illustrate the approach, a scheelite from Kalgoorlie, Western Australia, is hyperspectrally mapped and the cathodoluminescence is calibrated against microanalyses collected using a laser ablation inductively coupled plasma mass spectrometer. Trace element maps show micron scale zoning for the rare earth elements Sm3+, Dy3+, Er3+, and Eu3+/Eu2+. The distribution of Eu2+/Eu3+ suggests that both valences of Eu have been preserved in the scheelite since its crystallization 1.63 billion years ago.

Sign in / Sign up

Export Citation Format

Share Document