Rare Earth Element Concentrations Research Articles

Preparation of (Nd, Ce)-Fe-B Regenerated Magnets by In-Situ Restoration of Grain Boundary Structure Using Nascent Nd-Fe-B Powder.

Rare earth resource recycling is an important endeavor for environmental protection and resource utilization. This study explores the method of preparing regenerated magnets using waste magnets as raw materials based on existing processes. By utilizing existing Nd-Fe-B production equipment, various waste magnets are transformed into recycled powder. Next, nascent Nd-Fe-B powders with slightly higher rare earth content are selected as the repairing agent. The regenerated magnets are prepared by incorporating the nascent powder into the recycled powder. The focus lies in investigating the repairing effect of the nascent powder repairing agent on the microstructure of regenerated magnets and exploring the influence of sintering temperature and powder addition on the magnetic properties and microstructure of the regenerated magnets. The results showed that the nascent powder increased the proportion of grain boundary phases and effectively repaired the grain boundary structure of the regenerated magnets. In addition, the Pr element in the nascent powder replaces the Ce element in the recycled powder, which ultimately improves the magnetic properties of the regenerated magnet in a comprehensive manner. This study provides valuable insights and guidance for rare earth resource recycling and the preparation of regenerated magnets.

La-Modified SBA-15 Prepared by Direct Synthesis: Importance of Determining Actual Composition

Lanthanum (La) integration (at various nominal contents) in SBA-15 prepared under acidic medium was intended from corresponding direct nitrate addition during mesoporous silica formation. Materials were impregnated with Pt (1.5 wt%) and studied through several textural (N2 physisorption), structural (XRD, TG-DTG), and surface (FTIR, STEM-HAADF, SEM-EDS, NH3, and CO2 TPD) instrumental techniques. Pt-impregnated solids were tested in phenol hydrodeoxygenation (HDO, T = 250 °C, 3.2 MPa, batch reactor, n-decane as solvent). Catalytic activity (in pseudo-first-order kinetic constant, kHDO basis) was not directly related to Pt dispersion, which was not determined by nominal rare earth content. Determining the actual composition of modified SBA-15 materials is crucial in reaching sound conclusions regarding their physicochemical properties, especially when La modifier is directly added during mesoporous matrix formation, where efficient interaction among constituents could be difficult to get. Otherwise, results from some characterization techniques (N2 physisorption and FTIR, for instance) could be misleading and even contradictory. Indeed, extant modifier precursors, when under SBA-15 synthesis conditions, could affect the properties of prepared materials even though they were absent in obtained formulations. Performing simple compositional analysis could eliminate uncertainties regarding the role of various modifiers on characteristics of final catalysts. However, several groups have failed in doing so.

An unusual occurrence of carbonatites derived from the crust in the UHT granulite facies metamorphic terrain of Sri Lanka

The special calcite bodies (CBs) exposed within the ultrahigh temperature (UHT) granulite facies terrain in the Balangoda area of Sri Lanka preserve shreds of evidence for the generation of crust-derived carbonatite in the crust. The CBs are exclusively made up of massive calcites and appear as concordant bands extending tens of meters or as meso-scale isolated pockets hosting the massive dolomitic marble band. Various sizes of mafic and calc-silicate enclaves occur as rotated or tilted structures within the CBs. The contact between the CBs and the host marble is texturally and mineralogically gradational, while the contact between the enclaves and the CBs is sharp. The large-ion lithophile elements and rare earth element contents of the CBs show enrichment compared to the host marble, while depletion compared to typical carbonatites. Furthermore, the Sr content and C-O isotope values in CBs differ from those found in known carbonatites, hydrothermal carbonates, or metasomatic carbonates. We suggested that the crustal anatexis of marble should be hypothesized as the possible mechanism for the origin of the CBs. Microtexural evidence of the calcite grains shows indications of the melting of the host marble. The release of CO2-rich fluids from the collision and thrusting of HC over VC, or related metamorphic events, likely lowered the solidus of carbonates, triggering crustal anatexis of marble during UHT granulite facies metamorphism. The generated low viscous carbonate melt may have moved rapidly, resulting in a low degree of mixing of silicates and fragmentation and dislocation of enclaves. The results of the present study reflect the existence of anatexis of carbonates under extreme crustal conditions and provide a better understanding of the sources, migration paths and reservoirs of the carbon recycling processes.

Rare earth elements in apatite: A proxy for unravelling carbonatite melt compositions

Carbonatites are fascinating magmatic rocks because of their anomalous compositions, including the fact that some of these rocks host major rare earth element (REE) deposits. Despite much recent work, our understanding of their genesis and the composition of initial carbonatite melts is hindered by two major obstacles: most carbonatites we see are intrusive rocks, and they are commonly affected by metasomatic overprint. Here, we report experimental data in which we use apatite as a geochemical proxy to see back through crystallization and metasomatic events, thus making it possible to decipher the composition of carbonatite melts. We determined partition coefficients between apatite and carbonatite melts for a broad range of elements. The Na-rich nature of carbonatite melts plays an important role in apatite-melt partition coefficients, which are in the range of 1–7 for Sr, Y and REE in carbonatite systems. Using our new experimental data combined with >700 apatite composition data from carbonatites in various geodynamic settings, we show that carbonatite melt REE contents vary by more than two orders of magnitude. This variation cannot be solely produced by crystal-melt fractionation, implying that some carbonatite melts must be REE-rich or REE-poor initially, and that they mostly remain so during differentiation. We conclude that the degree of REE enrichment reflects carbonatite melts produced by immiscibility from variably differentiated alkaline magmas.

Features of Distribution of Rare-Earth Elements in Coals of the Far East

For the first time, the distribution of rare earth elements (REE) has been studied in detail for a number of coal facilities (30 deposits, 650 samples of coal and 210 samples of carbonaceous rocks). The ubiquitous presence of elevated concentrations of REE in coals has been noted. The REE mineral cluster in coals includes the association: ash content of coals – SiO2 – K2O – Al2o3 – TiO2 – Sc – Y – Dy – Ho – Er – Tm – Yb – Lu, and the association La – Ce – Pr – Nd – Sm – Eu – Gd – Tb. The presence of these elements of the mineral part of the coals is preferably in the composition of phosphate minerals – monazite and apatite (according to electron microscopy with microanalysis, the correlation of REE with P2o5). The content of individual REE in humic acids isolated from coals and fractions of coals of different densities has been studied. The specific role of organic matter(s) in the concentration of REE, their presence in the humus component of S and in low-ash coals is shown. Selective accumulation (fractionation) of heavy REE by organic matter has been experimentally established for the first time. Two genetic types of REE mineralization have been identified in coals: mainly terrigenous (hydrogenic) and tufogenic. The increased concentrations of REE in coals are due to the influence of the petrofund. The deposits were ranked according to the degree of prospects for REE based on an assessment of the resource potential of associated REE in the coals of the studied brown coal deposits. REE raw materials (lanthanides in coal ash) differ significantly from traditional types of rare earths ores by an incomparably large relative amount of heavy REE (on average 3–4 times), sometimes reaching 46% of the total REE content. Thus, coal ash is a unique non–traditional source of heavy lanthanides – more rare, valuable and expensive. The coals of the studied deposits should be considered as associated raw materials for rare earths.

POTENSI ANCAMAN HILANGNYA KANDUNGAN MINERAL ALAMI (TENORM) DI WILAYAH PENGHASIL TAMBANG KABUPATEN BANGKA TENGAH

The community in Central Bangka Regency carried out an increase in illegal mining in 2021, which could potentially threaten the loss of strategic natural resources. Rocking table miners in Central Bangka Regency produce zircon sand, tin sand, monazite, ilmenite, and tailings, which are potential natural resources containing rare earth metal elements. This research aims to analyze the radioactive content of the minerals zircon sand, tin sand, monazite, ilmenite, and tailings as a threat to human health. The research showed that monazite samples from all villages still had a lot of rare earth metals in them, like yttrium (Y), lanthanum (La), cerium (Ce), samarium (Sm), neodymium (Nd), and gadolinium (Gd). The test results showed that monazite had the highest average concentrations of Rare Earth Elements (REEs), with values of 10.27±3% for La, 12.15±3% for Ce, 24.40±3% for Sm, 7.37±3% for Nd, and 0.69±3% for Gd. For tin samples, the average (Ce) was 2.79±3%, zircon samples had an average (Ce) of 4.33±3%, and (Nd) 1.04±3%. In the ilmenite samples, the average value (Y) was 6.64 ± 3%. Monazite has the most rare earth metal elements, but it has a very low selling price. Monazite plays a crucial role in safeguarding and preventing the loss of strategic natural resources and health threats. It provides policy advice to related institutions through various roles and functions, including investigation, early prevention, and forecasting of these threats.

Fate and potential ecological risk of rare earth elements in 3000-year reclaimed soil chronosequences

The introduction of anthropogenic inputs into natural systems may lead to enduring alterations in the innate characteristics of Rare Earth Elements (REEs). Against this backdrop, the evolutionary processes and environmental drivers of REEs in soil remain uncertain. A 3000-year soil chronosequence with uniform parent material was established in reclaimed farmland along the Yangtze River, reconstructing, for the first time, the dynamic processes of REE accumulation and fractionation over a long-time scale. Analysis of 122 soil samples showed REE concentrations ranging from 146.00 to 216.56 μg/g. Based on reclamation duration, three significant stages of REE evolution were identified: natural leaching, rapid accumulation, and stable accumulation with differentiation. Reclaimed soil after 3000 years exhibited a 14.1 % increase in REE concentrations compared to fresh sediments, attributed to anthro -pedogenic processes. Moreover, Heavy Rare Earth Elements (HREEs) accumulated faster than Light Rare Earth Elements (LREEs), particularly in deeper soils (60–100 cm), where HREE concentrations rose by 34.3 %, mainly due to acidic environments promoting HREE fixation. Additionally, the potential ecological risk posed by REEs heightened with reclamation duration, with HREEs exhibiting a sensitivity of 83 % to 94 %. Our findings stress the urgency of carefully monitoring exogenous REEs introduced through anthropogenic activities, particularly HREEs.

Palaeoenvironmental implications of a turritelline-dominated assemblage from Upper Cretaceous carbonate rocks of Narmada Basin, India

Turritelline-dominated assemblages (TDAs) occur in modern siliciclastic seas within shallow depths, under normal to below normal salinity, high nutrient flux, high ocean upwelling current and/or runoff and cool water conditions. Similar assemblages in carbonate sediments are rare in modern oceans. However, TDA in carbonate rocks are common during the Cretaceous. In this study, we report the presence of a TDA in the late Turonian Nodular Limestone Formation of the Bagh Group, Narmada Basin, central India. An unusually small species of Turritella, T. bardhani Halder, n. sp., is described from the TDA. The TDA, in terms of host rock microfacies and taphonomy, indicates shallow water to intertidal, low to moderate energy, eutrophic to mesotrophic conditions, that prevailed in restricted lagoonal to marginal lagoonal, back-reef environments. The turritellines, based on trace elements and Rare Earth Elements concentration, thrived under dysoxic conditions and experienced above-normal marine salinities. The preferences of modern TDAs do not fully represent such past ecological and lithological conditions, indicating an example of a non-uniformitarian shift in habitat.

Incorporation of Multi‐Elements Into Diatom Frustules in the Scotia Sea, Antarctica, Since the Last Glacial Maximum

AbstractThe glacial‐interglacial cycle of elements and the linkage with biological production is very important. Nonetheless, records on incorporation of elements into diatom frustules are very poor in the Southern Ocean where diatom productivity is very high. As a result, there is a big gap in our understanding of elemental cycles in association with biological production and the controlling mechanisms. Here, we documented concentrations of major, trace, and rare earth elements of diatom frustules in two cores collected from the Southern Ocean since the Last Glacial Maximum to understand changes of incorporation of these elements into diatom frustules and to investigate mechanisms for changing incorporation. We found that there are three types of glacial‐interglacial variation patterns. Most elements showed increased (decreased) concentrations during the glacial period (interglacial) with decreased (increased) diatom production in the surface water following the variation pattern of magnetic susceptibility, whereas P, Ge, and Sb showed the opposite trend following the variation pattern of biogenic opal. Li, Ni, Ag, W, U, and I showed no clear glacial‐interglacial variation pattern. These different variation patterns imply that elemental incorporation into diatom frustules are also different according to elements. Our results revealed that biologically mediated removal of most elements from surface water to deep‐sea is comparable between glacial (low diatom production with high elements assimilation) and interglacial (high diatom production with low elements assimilation) periods in the Southern Ocean. However, more removal of P, Sb, and Ge in the surface water by diatoms occurs during interglacial periods in the Southern Ocean.

Tin-polymetallic mineralization and granitic rocks in the Nanling daping mining area: Geochemical and geochronological constraints

The Daping polymetallic deposit in the Nanling is a recently discovered deposit with significant potential in the Dayishan area. High-precision geochronological studies indicate that the emplacement ages of two fine-grained porphyritic (containing tourmaline) biotite granite units are 153.2 ± 0.9 Ma and 152.3 ± 1.0 Ma, representing products of the fifth magmatic activity in the Dayishan intrusion. The cassiterite U-Pb ages from the residual skarn type and greisen-type tin ores are 153.4 ± 3.6 Ma and 150.22 ± 0.37 Ma, respectively, and they are consistent within the error range, both belonging to the Yanshanian Early period. Petrogeochemical analyses of the granite reveal characteristics of high silica content (73.56 ∼ 75.91 %), alkali (K2O = 4.04 ∼ 5.58 %, Na2O = 2.22 ∼ 3.67 %), low calcium (0.42 ∼ 0.80 %), low magnesium (0.075 ∼ 0.29 %), and peraluminous nature (A/CNK = 1.26 ∼ 1.35). The rare earth element (REE) contents range from 35.78 × 10-6 to 111.57 × 10-6, with δEu values between 0.006 and 0.026, LREE/HREE ratios of 2.23 ∼ 3.41, and (La/Yb)N values of 1.20 ∼ 2.42. The granite is enriched in elements such as Rb, K, Th, U, Nd, Hf, and depleted in Ba, Sr, P, Nb, Ti, indicating strong crystal differentiation in the area. Sr, Nd, and Hf isotope studies show that the granite samples have ISr values of 0.67612–0.70040, εNd(t) values of −5.83 ∼ -8.23, εHf(t) values of −6.1 ∼ -1.9, (Nd)TDM2 values ranging from 1361 to 1573 Ma, and (Hf)TDM2 values ranging from 1147 to 1408 Ma. It is proposed that the Dayishan intrusion originated from the mixing of a mid-Paleoproterozoic mafic rock and a metamorphic sedimentary source region, with the latter being predominant. The detachment of source rocks from the mantle reservoir occurred in the mid-Paleoproterozoic. Combining lithological, petrogeochemical, and comparative analyses, it is classified as a highly fractionated A-type granite formed in a local extensional setting related to the subduction of the Pacific Plate. Additionally, this paper constructs a ore-forming model for the Daping tin deposit, aiming to provide reference for regional rare metal ore exploration.

Magmatic degassing and fluid metasomatism promote compositional variation from I-type to peralkaline A-type granite in the late Cretaceous Fuzhou felsic complex, SE China

Abstract A-type granites generally have much lower water, higher temperature, and incompatible element concentrations than I-type granitoids. Yet it remains unclear why I-A-type granitic complexes occur in convergent plate margins. Here we conduct geochemical analyses on apatite and mafic minerals from the late Cretaceous I-A-type granitic complex in Fuzhou area, SE China, aiming to decipher differentiation, fluid metasomatism, and degassing that primarily control the compositional diversity of felsic magmas. Apatites in both rock types are F-rich and show large H2O and δD variations, i.e., 341–3892 ppm H2O and –325 to +336‰ δD in I-type granitoids; 67–1366 ppm H2O and –251 to +1439‰ δD in A-type granites. H2O in apatite is negatively correlated with La/Sm and Sr/Y in the I-type granitoids, whereas it is positively correlated with Ce and total rare earth element (REE) concentrations in the A-type granites. Once H2O increases up to hundreds of ppm, both rock types show a rapid decrease of H2O/Ce, an increase of F/Cl, and extensive H isotope fractionation. Arfvedsonite occurs as a late crystallizing mineral in the A-type granite and has much higher contents of Na2O, K2O, F, and high field strength elements (HFSE) than hornblende in the I-type granitoids, indicating the addition of F-HFSE-rich alkaline fluids during its magmatic evolution. The consumption of arfvedsonite and formation of aegirine further indicate the role of fluid metasomatism and H2 degassing via a reaction of 3Na3Fe5Si8O22(OH)2 + 2H2O = 9NaFeSi2O6 + 2Fe3O4 + 6SiO2+5H2. The combined geochemical data demonstrate that the systematic differences in mineral assemblage, whole-rock composition, magma temperature, H2O content, and δD of apatite between the I- and A-type granites are likely attributed to varying degrees of differentiation, fluid metasomatism and magmatic degassing. The I-type granitoids experienced hornblende, biotite, plagioclase, K-feldspar, and apatite fractionation and close-system degassing. The A-type granite was likely formed from the I-type monzogranitic magma that was metasomatized by the mantle-derived F-HFSE-rich alkaline fluids to produce the peralkaline magma, which further experienced K-feldspar + plagioclase + biotite + apatite fractionation and open-system degassing. Further numerical estimation indicates that the primary magma of Fuzhou granitic complex contained ~3.0 wt% H2O, and the lower water content of A-type granite was likely attributed to strong degassing during its emplacement. Our results indicate that some peralkaline A-type granites can be generated from relatively water-poor I-type granitic magmas by fluid metasomatism and degassing.

Removal and Recovery of Europium with a New Functionalized Mesoporous Silica-Based Adsorbent

The discharge of acid mine drainage (AMD), characterized by a high concentration of rare earth elements (REEs), poses a significant threat to the health of ecosystems surrounding water sources. The global market demand for REEs has experienced a notable surge in the past decade. Consequently, recovering REEs from waste streams like AMD not only benefits the environment but also offers financial advantages. Europium (Eu), the rarest among REEs, constitutes only 0.1% w/w in monazite and bastnaesite ores. Eu is extensively used in the production of phosphors, alloys, and additives, and is a critical raw material for developing smart devices, ranging from high-resolution color screens to circuitry. Traditional adsorbents typically exhibit limited selectivity towards REE recovery. Mesoporous silica materials, such as SBA15 (Santa Barbara Amorphous-15), provide excellent tunability and modification capabilities, making them an attractive and cost-effective alternative. This research focused on two key aspects: (i) evaluating the dynamic adsorption column performance of granulated SBA15–NH–PMIDA to preferentially recover Eu, and (ii) employing mathematical modeling to optimize the dynamic adsorption column’s operating conditions for real-world applications with a minimal number of experimental runs. Granulated SBA15–NH–PMIDA was chosen as the adsorbent due to its high adsorptive capacity and selectivity in capturing Eu. The study revealed that granulated SBA15–NH–PMIDA exhibited 57.47 mg/g adsorption capacity and an 81% selectivity towards Eu. Furthermore, SBA15–NH–PMIDA demonstrated preferential adsorption toward Eu in complex multi-component solutions, such as AMD. The linear driven force approximation model (LDFAM) provided an acceptable simulation (R2 > 0.91) under varying operational conditions. This validates the use of the model as a tool to effectively simulate and optimize column experiments that used granulated SBA15–NH–PMIDA to recover Eu.

Hydrothermal enrichment of rare earth elements in the Lower Permian Lijiatian bauxite deposit, southern China

Bauxite deposits are an important source of Al and also host a variety of critical metals, including rare earth elements (REEs). However, the parent rocks of bauxite deposits generally have low REE contents, leading to uncertainty over the REE sources and enrichment mechanisms. In this study, we report high REE (2095 ppm; Ce = 1340 ppm) contents in the Lijiatian bauxite deposit in Luxi County, western Hunan Province, South China. The Lijiatian bauxite deposit is the largest deposit in Hunan Province, with a total Al resources exceeding 7 × 106 tons. The ore-bearing strata in the lower Permian Liangshan Formation (ca. 275 Ma) are comprised a 3–5-m-thick bauxite layer (bauxite ore/clay) and an underlying 4–8-m-thick Fe layer (Fe ore/Fe-rich clay). The high REE contents in the bauxites can be attributed to the widespread presence of bastnäsite. The bastnäsite commonly coexists with authigenic chlorite, which formed at temperatures of 221–285 °C, indicative of a hydrothermal origin. Uranium–Pb dating of the bastnäsite yielded an age of 141.4 ± 7.0 Ma, indicating a hydrothermal overprint occurred during the Early Cretaceous, which resulted in the enrichment of REEs in the bauxites. The high contents of REEs, Ba, and P in the Cambrian Niutitang Formation black shales indicate it was a potential source of these elements for bastnäsite and coexisting barite and apatite. The deep-seated hydrothermal fluids (enriched in HF, CO2, and H2S) associated with the late Yanshanian extensional tectonic event in South China (155–123 Ma) ascended along fractures. The ascending fluids interacted with the black shales, extracting REEs, Ba, and P. When the fluids reached a certain depth, they mixed with the infiltrating basinal waters to form a mineralising fluid. The fluid then migrated towards the bauxite layers, underwent cooling and depressurisation, and precipitated bastnäsite, barite, apatite, and chlorite. We propose that a hydrothermal event led to the enrichment of REEs in the bauxites in Hunan Province. Considering the scarcity of REEs in the parent rocks of bauxites worldwide, hydrothermal activity likely has a key role in REE enrichment in bauxites.

The 2.03–2.02 Ga arc–back-arc mafic magmatism from the Zhongxiang Complex, northern Yangtze Block: Implications for Columbia supercontinent assembly

To better understand Paleoproterozoic tectonic processes in the Yangtze Block during the assembly of the Columbia supercontinent, an integrated geochronological and geochemical study of amphibolite facies mafic rocks exposed in the Zhongxiang Complex in the northern Yangtze Block is presented. Based on trace element and rare earth element (REE) characteristics, these mafic rocks can be divided into two coeval groups. The MORB-like mafic rocks show flat REE patterns and are enriched in large-ion lithophile elements (e.g. Rb, Ba, K, Sr). Their zircon ɛHf(t) values range from + 3.43 to + 4.90. The other mafic rocks are arc-like and have elevated REE contents and display relatively light REE enriched patterns, as well as depletion in high field strength elements (e.g. Nb, Ta, Ti). The zircon ɛHf(t) values of the latter group range from + 0.17 to + 2.68. Zircon U-Pb dating yielded a weighted mean 207Pb/206Pb age of 2029 ± 15 Ma for the MORB-like mafic rocks, and 2023 ± 14 Ma for the arc-like mafic rocks, respectively. The elemental and isotopic characteristics indicate that the MORB-like mafic rocks may be derived from a depleted asthenospheric mantle source, whereas its counterpart with arc-like signatures originated from a lithospheric mantle source. The low (La/Yb)CN (1.10–2.84) and Sm/Yb (0.99–1.29) ratios indicate that the mafic rocks are formed by partial melting of spinel lherzolite mantle. Combined with other geological observations, these mafic rocks are inferred to constitute part of a mid-Paleoproterozoic continental arc–back-arc basin system. The 2.03–2.02 Ga mafic rocks from the northern Yangtze Block indicate that the continental margin experienced subduction in response to assembly of the Columbia supercontinent.

Evaluation of garnet phenocrysts in volcanic rocks (Görece/İzmir – Western Türkiye) for their usability as a semi-precious gemstone by multi-analytical methods

Garnets are observed as phenocrysts in blocky rhyolites of Cumaovası Volcanites and are reddish-blackish in color, show vitreous luster, and have dodecahedron forms varying between 0.5 and 2.0 cm in size. In optical microscope investigations, they exhibit fractured structures and contain quartz, hematite, chlorite, and acicular rutile inclusions. Garnet phenocrysts are highly consistent with spessartine-type garnet end members in the Raman spectrum. This result is supported by the mineral chemistry results determined as spessartine (Sps)0.50–0.52 almandine (Alm)0.47–0.48 grossular (Grs)0.01–0.02. In the chondrite, primitive mantle, and Mid-Oceanic Ridge Basalt normalized multi element variation diagrams, garnet phenocrysts show enrichment in all elements (except Sr, K, P, and Ti). In contrast, in the upper continental crust normalized multi element variation diagram, garnet phenocrysts show depletion in large ion lithophile elements (Rb, Ba, K, and Sr) relative to high field strength elements. They exhibit slight enrichment in light rare earth elements ((La/Sm)N = 0.11–1.07) relative to heavy rare earth elements ((Sm/Yb)N=0.78–0.97). Furthermore, garnet phenocrysts have significant negative europium (Eu) ((Eu/Eu*)N = 0.01–0.02) and mildly positive cerium ((Ce/Ce*)N = 2.43–13.77) anomalies indicating hot and reduced magma conditions. The Y/Ho ratios have ranged from 18.9 to 20.3 and are close to the chondrite value. The zircon saturation temperatures (TZr) of the garnet’s host rock was determined to be 756 °C. As a result of mineralogical, geochemical and gemological studies, it was concluded that Görece garnet phenocrysts have glassy luster and semi-transparent dodecahedral crystal shapes, so they can be classified as semi-precious gemstones. In addition, the rare earth element content of the garnet phenocrysts is similar to that of industrial garnet sands and it is thought that they may have potential.

Grain size control on organo-clay complexation and REE fractionation in the Paleozoic strata of the Permian Basin (West Texas, U.S.A.)

As a major component of mudstone, clay minerals are known to conserve organic matter (OM) as well as a range of trace elements through the mechanisms of adsorption, encapsulation, and/or intercalation. The associations of the clay minerals on one hand and trace elements and OM on the other hand impact the diagenetic evolution of such rocks and is of substantial importance for their characterization and assessment. Subsurface core samples collected from Late Paleozoic mudstone within the Permian Basin of Texas were separated into four grain size fractions (>2 µm, 2 to 1 µm, 1 to 0.6 µm, and <0.6 µm) to determine the clay mineralogy, OM abundances, and rock geochemistry using a suite of diffraction, spectroscopic, and chemical analysis. All separates were largely consisted of illite-smectite (I-S), illite-tobelite-smectite (I-T-S), mica/illite and chlorite coupled with some minor quartz and feldspar. The smectite component of I-S was shown to increase with decreasing grain size fractions. Additionally, t he rise in the content of smectite interlayers correlated with an increase in the total organic carbon (TOC) content towards the finest grain size separates in all samples. This suggested that a significant portion of the TOC content resided in the fraction below 2 µm and that smectite interlayers promoted the preservation of OM. Rare earth elements (REE) concentrations were found to be the highest in the finest grain size separates and align with an increased content of smectite interlayers, denoting a plausible interaction between the two. Further on, REE and TOC concentrations display a significant positive correlation in all size fractions and increase with respect to smectite interlayer content. This three-component relation suggests the REE adsorption to illite-smectite was likely promoted by OM. Understanding the close relation between the clay minerals, OM, and trace element content is indicative of polyvalent cationic bridging, ligand exchange, and organo-metallic complexation, which eventually l eads to the enrichment of OM and fractionation of REE in mudstone.

Rare earth elements as tracers: A study on post-wildfire effects in soil by neutron activation analysis

This study investigated using rare earth elements as tracers to study wildfire impacts. The study area was Antalya, located in the Mediterranean region of Türkiye. This region is known for the frequent occurrence of wildfires, which cause significant damage to the flora and fauna of the area. A series of wildfires occurred in the region in 2016. Soil samples were collected from the affected areas to understand these wildfires' impact better. Instrumental neutron activation analysis was used to analyze the samples. The study found that the north-facing aspect had higher concentrations of rare earth elements. This could be because north-facing aspects are cooler and more humid, with less erosion, leading to better ecological restoration and less transportation of rare earth elements.

Specification for Light Rare Earth Concentrates Prepared from Egyptian Crude Monazite Spectrophotometrically

Specification for Light Rare Earth Concentrates Prepared from Egyptian Crude Monazite Spectrophotometrically

Petrology and association of rare earth elements in magmatically altered high-ash coal of Indian origin

The extraction of valuables from waste has gained momentum. Thermal influence alters both the organic and inorganic components of coal. Insufficient knowledge on the association of rare earth elements (REEs) with the parent matrix of thermally altered high-ash coals (63% ash) limits the potential for such coals being utilized for isolation of valuables. In this study, we analyzed the distribution and occurrence modes of REEs within a magmatically altered high-ash coal via nine-step sequential extraction, combining Tessier and BCR methods. The total concentration of REEs in the coal sample, on whole coal basis, was found to be 820 ppm, which is significantly higher than the world average. Major mineral oxides were deduced to be those of Si, Fe, Al, Ca, Mg, and Ti. Sequential extraction confirmed that about 66% of HREE and 25% of LREE were included in the residual fraction. LREEs were concluded to be primarily in ionic form, whereas HREEs were speculated to be associated with the TiO2 phase. XRD analyses showed that thermal alteration affected the dolomite phase specifically, which selectively got removed where carbonate-bound elements were assessed. Petrographic analysis supported the magmatic influence and demonstrated the presence of mosaic structures and pores containing unfused vitrinite, with a reflectance value of 3.6. To summarize, the present study pertaining to delineation of association of valuables in high-ash heat-altered coals from an Eastern coalfield in India can potentially open up new avenues for utilizing such coals, which are otherwise considered waste.

The depositional redox conditions of Fe‐speciation reference materials (BHW and WHIT) using redox‐sensitive trace metal enrichment

Iron speciation has emerged as a robust proxy for discerning oceanic redox conditions; nonetheless, it is subject to certain limitations. Specifically, the applicability of the degree of pyritization is contingent upon the presence of unequivocal evidence of an anoxic water column and its discriminatory capacity is limited to distinguish between ferruginous (anoxic) and euxinic conditions. This study highlights that through the integration of redox‐sensitive trace metal enrichment data with Fe‐speciation data, the depositional redox conditions for marine sediments can be established with greater certainty. Recently, a set of dedicated geological reference materials (BHW and WHIT) have been developed for validating the Fe‐speciation analytical results for redox reconstruction studies; however, to the best of our knowledge, these reference materials are not characterized for trace and rare earth elements (REEs). In this connection, the BHW (oxic) and WHIT (anoxic) reference materials are measured for major, trace and REEs. After careful statistical considerations for these reference standards, a complete set of trace and REEs is reported. Furthermore, considering BHW and WHIT as oxic and anoxic end‐members, respectively, the utility of trace metal enrichment and Fe‐speciation data in combination has been discussed. The trace and REE concentrations of BHW and WHIT reported in this study will enhance their applicability as a reference material to understand ocean chemistry and the oxidation state of the ancient oceans.