Low Al2O3 Contents Research Articles

Petrogenesis and an Evaluation of the Melting Conditions of the Late Permian ELIP Picrites, SW China: Constraints Due to Primary Magma and Olivine Composition

The late Permian Emeishan large igneous province (ELIP) in SW China is a melting product of the Emeishan mantle plume. Recently, it has been debated whether peridotite or pyroxenite is the dominant lithology of the mantle source in the ELIP. To address this, systematic analyses of bulk-rock and coexisting spinel and olivine compositions were conducted on picrites from Lijiang–Yongsheng, Dali–Binchuan, Yumen, Muli, and Ertan. The ELIP picrites exhibit positive TiO2–CaO and negative MgO–CaO correlations, as well as low FC3MS values (−0.24–0.1), supporting a peridotite-dominated mantle source. This lithology of the mantle source is also supported by the high 100 × Mn–Fe (1.43–1.73) and Mn–Zn (13.6–18.4) values but low 10,000 × Zn–Fe (8.0–12.7) ratios of the olivine phenocrysts. The estimated mantle potential temperature for Lijiang, Yongsheng, Yumen–Ertan, Muli, and Dali–Binchuan picrites decreased away from Lijiang and Yongsheng, suggesting that the Lijiang and Yongsheng areas were the center of the ELIP. The Lijiang–Yongsheng primary magma shows similar SiO2 content but lower Al2O3 contents (average of 8.24 wt.%) and higher MgO contents (average of 21.42 wt.%) than those of Dali–Binchuan primary magma (Al2O3: 9.86 wt.%; MgO: 19.02 wt.%). Also considering the high Gd–Yb (average of 3.05) and La–Yb (average of 14.61) ratios and mantle potential temperature (average of 1599 °C), we proposed that Lijiang–Yongsheng lavas are produced via the melting of a garnet–peridotitic mantle. In contrast, the Dali–Binchuan lavas with low Gd–Yb (average of 1.91) and La–Yb (average of 5.88) ratios can be explained by their formation in the garnet–spinel transition zone of a peridotitic mantle. The Yumen–Ertan primary magma displays similar mantle potential temperature (average of 1600 °C), Al2O3 and FeO content, and Gd–Yb ratios to those of Lijiang–Yongsheng lavas, indicating that YumenvErtan primary magma may be attributed to the partial melting of garnet with minor peridotite. Therefore, heterogeneous plume-head mantle sources lead to the evaluation of melting conditions of the late Permian ELIP picrites.

Al2O3 Concentration Effect on Deep Hydrodesulfurization of 4,6-Dimethyldibenzothiophene over NiWS/Al2O3-ZrO2 Catalysts.

The Al2O3 concentration effect over NiWS/Al x Zr100-x catalysts was investigated for deep hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT). The sol-gel method changed the wt % Al2O3 concentrations used to synthesize the Al x Zr100-x supports. The NiWS/Al x Zr100-x catalysts were prepared with ammonium metatungstate hydrate and nickel(II) nitrate hexahydrate by sequential incipient impregnation, calcination, and H2S/H2 activation. The catalytic evaluation data fit a pseudo-first-order trend in the 4,6-DMDBT HDS reactions. In the oxide phase, the catalysts presented Ni and W species in tetrahedral (td) and octahedral (oh) coordination, with the oh species prevailing as a function of the Al2O3 amount. The lower amount of Al2O3 can facilitate the "Type II" NiWS phase formation by weakening the interaction of the W-O-Al bond and promoting W and Ni species sulfidation. In the sulfide phase, catalysts with (oh) coordination and surface WO X species promote the formation of WS2 and NiWS species during the catalyst activation step. This species favors the reaction yield, where the hydrogenation route is predominant, with the highest initial reaction rate using the NiWS/Al25Zr75 catalyst. A direct correlation was found between high hydrogenation/hydrogenolysis ratio values and low Al2O3 concentrations.

Mesoproterozoic depleted spinel peridotites metasomatized by high-K hydrous melt in the Patagonian back-arc

Here we report the first investigation of spinel-bearing mantle xenoliths from Los Gemelos volcano, Canquel Plateau, Patagonia. They are highly-depleted Mesoproterozoic (ReOs model ages of 1.3–0.9 Ga) harzburgites and clinopyroxene-poor lherzolites characterized by typical indicators of partial melt extraction, such as low whole-rock Al2O3 and CaO contents (<1.5 wt%), high Mg# of silicate phases (90–95), and Cr-rich spinel (Cr# 0.20–0.42). Depletion of incompatible highly siderophile elements (Re, Ru, Pd) relative to the primitive upper mantle supports high degrees of melt extraction. The occurrence of phlogopite and K-rich alkaline glass veins with high- and low-SiO2 compositions is clear evidence of modal metasomatism. The light rare earth element (LREE) enrichment in clinopyroxene, as well as the whole-rock U-shaped REE pattern, confirms cryptic metasomatism. This melt-rock interaction is corroborated by major (i.e., Mg# vs. basaltic elements) and trace (i.e., La/YbN vs. Sr/Y and Ti/Eu; and Sr vs. Ti/Eu) element contents of pyroxenes. The calculated compositions of melts in equilibrium with clinopyroxene coexisting with phlogopite suggest interaction with slab-derived materials. This metasomatism has been generated by a chromatographic fractionation-reaction process, from deep to shallow mantle domains. The percolation of a high-K hydrous magma probably is associated with the upwelling of asthenospheric material through a slab-window, which caused partial melting of oceanic crust and overlying sediments during the Paleocene. The varying intensities of metasomatic imprints recorded by mantle xenoliths from Los Gemelos provide valuable insights into the interaction of slab-derived materials near the lithosphere-asthenosphere boundary, at a distance of ∼600 km from the Andean volcanic arc.

Formation and removal mechanism of SiO2-MnO-Al2O3 inclusions in Al-killed 42CrMo4 wind turbine bearing steel forgings

SiO2-MnO-Al2O3 (SMA) inclusions were identified in the defective areas during the ultrasonic inspection of Al-killed 42CrMo4 wind turbine bearing steel forgings. To explore their formation mechanism, we systematically sampled 42CrMo4 steel through industrial experiments, analysing SMA inclusions’ morphology and composition at various stages. Thermodynamic calculations were also employed to assess the origin and formation of these inclusions. It was observed that these inclusions primarily formed during electric arc furnace tapping, where the mass ratio of SiO2 to MnO was close to 1, while the Al2O3 content varied. Despite undergoing the ladle furnace and vacuum degassing (VD) refining processes, these inclusions persisted in the molten steel. Following the conclusion of electric furnace smelting, the dissolved oxygen content in the molten steel could reach 193 ppm. During the tapping process, high oxidising steel comes into direct contact with silicon-manganese alloy. During this phase, the uneven distribution of Al content around the alloy results in the formation of SMA inclusions with varying Al2O3 content. Dynamic calculations suggest that in subsequent smelting processes, SMA inclusions with high Al2O3 content and large size are relatively easier to eliminate, while those with low Al2O3 content and small size are more likely to persist in the molten steel. During solidification, residual SMA inclusions agglomerate, forming larger sizes, consequently resulting in the ultrasonic inspection failure of 42CrMo4 steel forgings. After the process improvement, the SMA inclusions are greatly reduced and the effect is obvious.

Effects of Al2O3 content on the microstructure and performance of Inconel 625-xAl2O3 composite non-skid coatings by plasma enhanced high-velocity arc spraying

The efficient preparation of metal/ceramic composite coatings with excellent performance has been a hot research topic in the field of thermal spraying. In this study, a novel plasma enhanced high-velocity arc spraying (PE-HAS) technique is developed. A series of Inconel 625-xAl2O3 composite non-skid coatings are deposited by PE-HAS with different feeding ratio of alloy wire (1.6 mm in diameter) and ceramic powder (13.5 μm in average particle size). Specifically, the microstructure, mechanical properties, corrosion resistance and tribological performances of the coatings have been comprehensively investigated. Results indicate that all of the composite coatings with different Al2O3 contents are characterized by high densities, low defects (porosity≤3.52 %), strong bonding (≥50 MPa) and high friction coefficient (≤ 1.034). The coatings with low Al2O3 content feature a more homogeneous structure and superior bonding strength. The microhardness and wear resistance of the coatings increases significantly with increasing Al2O3 content, which should be attributed to the formation of many localised enhancement areas composed of different forms of Al2O3 phases. It is worth noting that the unique feedstock feeding method promotes the formation of the in-situ double-layer structure of coatings with high Al2O3 content, which further improves the wear and corrosion resistance. However, the friction coefficient gradually decreases when the Al2O3 content is too high, thus affecting the anti-slip performance of the coating.

Ultrahigh-temperature crustal anatexis and final cratonization in Eastern Hebei, North China Craton: Insights from ca. 2.46 Ga Taipingzhai enderbites

Charnockitic rocks are a suite of granulite-facies plutonic rocks that include dominantly granitic−tonalitic and partly dioritic rocks. The Na-rich endmembers of the charnockite series, including dioritic to tonalitic rocks, are also termed enderbites. Charnockitic rocks are the main component of the cratonic-type lower continental crust in Precambrian cratons worldwide. These rocks are generally considered to be products of the anatexis of the lower crust under high- to ultrahigh-temperature conditions and play a key role in stratification between upper and lower crustal layers as well as the cratonic stabilization (cratonization) of Precambrian continents, although further study is required to gather detailed information about these rocks. In this study, a group of igneous enderbites (dioritic−tonalitic charnockites) from Eastern Hebei, North China Craton, is investigated. Zircon U-Pb dating reveals that the enderbites formed at ca. 2.46 Ga, which is coeval with the regional granulite-facies metamorphic overprinting. The enderbites are primarily composed of clinopyroxene, orthopyroxene, plagioclase, and quartz, with minor amphibole, biotite, K-feldspar, and Fe-Ti oxides. The rocks are characterized by high Fe2O3T + MgO (9.80−15.9 wt%), Cr (71.0−292 ppm), and Ni (41.2−107 ppm) contents, as well as low Al2O3 (13.9−16.6 wt%) and K2O (1.07−2.43 wt%) contents, with high Na2O/K2O ratios (1.51−4.43) and low Sr/Y (24.5−49.5) ratios. Moreover, these rocks are enriched in light rare earth elements (LREEs), (La/Yb)N = 8.06−17.8, and yield weak Eu anomalies, (Eu/Eu* = 0.80−1.18), with negative Th, U, Ta, Nb, and Ti anomalies. Various mineral thermobarometers, oxybarometers, and hydrometers are used to constrain the crystallized P-T-ƒO2-H2O conditions of the enderbites. These rocks crystallized at high temperature (860−1000 °C), crystallization pressure (8.0 ± 1.0 kbar), and H2O-poor (1.5−2.4 wt%) conditions, with oxygen fugacities (ΔQFM) of 0.0−3.0, which suggests “hot” (high-temperature) and “dry” (water-poor) crystallization conditions. The enderbites also have heterogeneous in situ zircon Hf-O isotopic compositions: εHf(t) = 2.4−7.5; δ18O = 5.78‰−7.74‰. These new data, combined with trace element characteristics, suggest that the enderbites were derived from the partial melting of metabasites, and that assimilation and fractional crystallization controlled the compositional variation in the enderbites. Further thermodynamic and geochemical modeling suggests that the anatexis of Mg-Fe−rich metabasite under ultrahigh-temperature (&amp;gt;1000 °C) and H2O-poor (1.0−1.5 wt%) conditions at a low crustal depth (∼9.0 kbar) could yield a melt composition comparable to that of the observed enderbites. Postcollisional lithospheric extension and mafic magma underplating prompted the partial melting of lower crustal metabasite at ultrahigh temperatures and normal lower crustal depths, resulting in the formation of enderbites. This study demonstrates that the enderbites could be formed by ultrahigh-temperature anatexis of metabasite with amphibole dehydration melting (Pl + Amp → Opx + Cpx + melt) and offers robust evidence of the genetic links between the ultrahigh-temperature anatexis of basic rocks and the generation of enderbites. In addition, the occurrence of ca. 2.46 Ga enderbites may mark the final cratonization of the North China Craton, and the ca. 2.50−2.45 Ga tectono-thermal event was an ultrahigh-temperature metamorphic-anatexis process rather than simple regional granulite metamorphic overprinting. Therefore, the generation and emplacement of enderbites involved not only a magmatic process but also an element redistribution process in the lower crust, which has important implications for stabilization of the North China Craton at ca. 2.5 Ga.

Petrology and Geochemistry of an Unusual Granulite Facies Xenolith of the Late Oligocene Post-Obduction Koum Granodiorite (New Caledonia, Southwest Pacific): Geodynamic Inferences

Pressure–temperature estimates of a xenolith found within a post-obduction granodiorite in southern New Caledonia provide evidence for subcrustal, granulite facies, peak crystallisation conditions (ca. 850 °C—8.5 ± 1.0 kbar), followed by isobaric cooling to 700 °C, and final decompression with partial rehydration at ca. 650 °C—3.5 kbar. The xenolith, dated at 24.7 Ma (U-Pb zircon), i.e., the same age as the granodiorite host rock, has low SiO2 (35.5 wt%) and high Al2O3 (33.2 wt%) contents, suggesting that it is the restite of a previous melting episode, while the elevated Ca (Ba and Sr) contents suggest mantle metasomatism. Although the concentrations of Rb, K, Ca, Ba, and Sr have been strongly modified, some geochemical (REE patterns and some “immobile” trace element ratios) and isotopic (Sr and Nd isotopic ratios, U-Pb zircon age) characteristics of the granulite facies xenolith are similar to those of the xenoliths found in other Late Oligocene intrusions in southern New Caledonia; therefore, this rock is interpreted to be related to an early magmatic episode. The rock protolith was emplaced and equilibrated at the base of the crust where it underwent ductile deformation. Younger ascending magma picked it up and they eventually crystallised together at a shallow crustal level, near the tectonic sole of the ophiolite. The recrystallisation and ductile deformation at ~8.5 kbar suggest that a rheological discontinuity existed at about 25–28 km, probably representing the Moho. It is concluded that a continental crust of normal thickness must have existed beneath New Caledonia at about 24 Ma, i.e., 10 Ma after obduction.

Unravelling the genesis and depositional setting of Neoproterozoic banded iron formation from central Eastern Desert, Egypt

The Neoproterozoic banded iron formations (BIFs) are widely occurred in the Egyptian Eastern Desert. This study integrates field observations, petrographic studies, geochemical data, and lead isotopes to construct the genesis and depositional environment of Wadi El-Mis hama BIF deposits. The iron layers, primarily of oxide facies within a volcano-sedimentary sequence, comprise magnetite-rich beds alternating with jaspilite or silicate laminae. The studied BIFs exhibit a dominant composition of SiO2 and Fe2O3t with relatively low contents of TiO2 and Al2O3. The positive correlation of REEs (La, Sm, Yb) with Zr and low concentrations of HFSEs (Ta, Nb, Th, Hf) indicate a primary formation mechanism of chemical precipitation, maintaining original geochemical signatures. Geochemical patterns show depletion in LREEs, enrichment in HREEs (La/YbPAAS = 0.08–0.12), and positive La anomalies (La/LaPAAS = 1.15–8.57), consistent with seawater influence. Additionally, various geochemical discrimination diagrams supported by elevated super-chondritic Y/Ho values (29.6–38.7), weak positive Eu anomalies, and low contents of transition metals (Cu and Zn), point to the interaction of low-temperature (&amp;lt;200°C) hydrothermal fluids (bearing Fe and Si) with seawater during the deposition of the BIFs. The lack of significant negative Ce anomalies along with low Ni/Co, U/Th, and Cu/Zn ratios, imply that the iron mineralization was precipitated from dysoxic to oxic conditions. The geochemical and Pb isotopic data suggest that the iron deposits formed in an extensional geodynamic setting (intra-oceanic arc basin environment) due to the subduction of the Mozambique Plate, with signatures closely matching other Precambrian Algoma-type BIFs.

The Petrography and geochemistry of iron-bearing units from Mingo’o area (Ntem complex, southern Cameroon)

The banded iron formation (BIF) of the Mingo’o region is located on the northern edge of the Congo Craton. They constitute a significant component of the southern Cameroonian Archean to Paleoproterozoic. Petrographic description indicates that the most characteristic facies of the Mingo'o BIFs are quartz-magnetite BIFs (QMB), which are mostly composed of magnetite and quartz. Geochemistry analyses show that the major elements of this BIF are very simple, with SiO2 and Fe2O3 representing 95.25 wt. % of the bulk rock on average. The low concentrations of Al2O3, TiO2, and HFSE reveal that these chemical sediments are detritus-free. According to Paerson's major element correlation matrix, there is a slight contribution of detrital material to chemical sediment, as confirmed by the strong positive correlation (r = 0.72) of Al and Ti, also by the binary diagrams Al vs. Σ(Y + Nb + Zr) with a weak positive correlation (r2 = 0.31) and Al vs. ΣREE with a zero correlation (r2 = 0.08), indicating that the detrital input was insignificant. The transition metals Zn, Cr, Sr, and V are among the trace elements with low enrichments. This suggests the direction of the volcanogenic hydrothermal input in chemical precipitates. The mean ∑REE concentration of the studied BIF is 26.74 ppm, with a range of 8.82 to 36.74 ppm. Pure chemical sediments are comparable to that. The shale-normalized patterns display minor positive europium anomalies, a sharp decrease in heavy REE, and enrichment in light REE. These geochemical characteristics suggest that the hydrothermal activity in the deep ocean, coupled with seawater, was the source of the Fe and Si. Low-temperature hydrothermal solutions play a key role in the studied BIF, as shown by the absence of a notable positive Eu anomaly. Ce anomalies are seen in the chrondrite-normalized REE patterns, which are characterized by LREE-enriched (mean LaCN/YbCN = 5.28) and HREE depletion (mean TbCN/YbCN = 1.04) patterns. This may indicate that the BIF within the Mingo’o region was formed in place of the basin towards redoxcline, alternating at different times and under various influences from the influx of seawater that has been oxidized.

Large-scale Mesoproterozoic iron formations in northwestern China

Iron formations (IFs) represent an economically important iron-rich rock type in the Precambrian geologic record. It is generally assumed that after ca. 1.85 Ga, large-scale IFs were not deposited for approximately 1.1 Gy. However, substantial IFs, including over 15 large- to small-scale iron deposits, have been identified recently in Northwest China, and they would constitute the largest Mesoproterozoic IFs globally if their Mesoproterozoic ages can be confirmed. Field observations reveal that these iron deposits are dominantly stratiform and stratoid within the thick clastic-carbonate and volcanic-sedimentary succession. The ores mainly comprise Fe-rich (specularite, hematite, and siderite) and Si-rich (jasper and quartz) minerals with banded or massive structures. Geochemical investigations of typical iron ores show high SiO2 and TFe2O3 and relatively low Al2O3 and TiO2 contents, indicating that they are primary chemical sediments with high hydrothermal and low detrital contributions. These features suggest that these iron deposits in the NQOB are typical IFs, which resemble the Archean and Paleoproterozoic IFs worldwide. New zircon U-Pb dating and lithostratigraphic correlations indicate that these IFs were deposited at ca. 1.1 Ga. The sizable ore reserves and Mesoproterozoic ages confirm that these IFs are the largest reported IFs for the billion years between 1.8 and 0.8 Ga. The large-scale Mesoproterozoic-aged IFs help fill the longest gap in Earth history where the IFs were thought absent from the geologic record and provide an unusual perspective to understand the reappearance mechanism of Precambrian IFs.

Retrogression of ultrahigh-pressure eclogite, Western Gneiss Region, Norway

Abstract. The Western Gneiss Region (WGR) in western Norway exposes ultrahigh-pressure (UHP) eclogites that occur repeatedly, within an area of high-pressure (HP) eclogites, without evidence of being separated by tectonic shear or ductile flow structures. We studied 10 eclogites from two northern UHP areas and the interjacent HP area to evaluate the significance of this pattern. The orthopyroxene in orthopyroxene-bearing samples has low Al2O3 contents (0.17 wt %–0.37 wt %), provided its grain boundaries were unaffected by partial recrystallisation or replacement. Classical geothermobarometry based on element partitioning between coexisting mineral phases suggests metamorphic conditions within the diamond stability field for the samples from both the HP and UHP areas. The primary clinopyroxene in the associated orthopyroxene-free eclogites contains aligned inclusions of either needle-shaped quartz ± pargasite or lamellar albite, which are absent from the secondary (symplectic) clinopyroxene. Reconstructed mineral compositions of the primary clinopyroxene obtained from grain cross-section surfaces using a scanning electron beam or image processing are non-stoichiometric, and they have higher Ca-Eskola and lower Ca-Tschermak components than the inclusion-bearing host clinopyroxene. The molar ratios of these endmembers are consistent with the needles in the primary clinopyroxene being formed from vacancy-bearing precursor clinopyroxene by the exsolution reaction 2 Ca-Eskola = Ca-Tschermak + 3 quartz during early eclogite-facies retrogression. Further retrogression partially transformed the needle-shaped quartz to irregularly shaped albite within the clinopyroxene and partially transformed both clinopyroxene generations to amphibole that occasionally preserves the needles. The similarity of both the maximum metamorphic conditions and the mineral exsolution microstructures in the eclogites from UHP and HP areas indicates a shared metamorphic history within the stability field of diamond, but a history that diverged during retrogression. Consequently, the alternations of UHP and HP areas in the WGR may have formed by a process that allowed for spatial variations in retrogression efficiency, such as the localisation of strain (recrystallisation) or fluid flow (diffusion) or both, rather than by tectonic stacking of UHP and HP units. Evidence for the UHP metamorphism of WGR crustal rocks is now found from NE to SW along the entire coastal section that covers previously recognised UHP and interjacent areas.

Mesoarchean synchronous emplacement of TTG gneisses and potassic granitoids in the Nyabessane granite-greenstone terranes, NW Congo Craton (southern Cameroon): Zircon U[sbnd]Pb geochronology, petrogenesis and tectonic implications

Archean granitoids played key roles in the generation and differentiation of the Archean continental crust and provide clues to understand crustal processes in the early Earth. Abundant Mesoarchean granitoids were emplaced in the Nyabessane granite-greenstone terrane (NGB), part of the Ntem Complex of the Northwest Congo Craton. They include charnockites, tonalite-trondhjemite-granodiorite (TTG), granitic and monzogranitic gneisses. Here, we present a geochemical and geochronological (zircon LA-ICP-SF-MS UPb) study of these granitoids to determine their petrogenesis and to better constrain the crustal evolution of the Ntem Complex. Field and petrographic observations indicate that most of these granitoids underwent extensive metamorphism and deformations, associated with anatexis. Zircon UPb dating results suggest that the charnockite, TTGs and granitic gneisses, and monzogranites have emplacement ages of 2910 ± 11 Ma, 2870–2865 Ma and 2852 ± 31 Ma, respectively. The charnockites have low SiO2 (55–58 wt%) and high Al2O3 (16–18 wt%), CaO (7–8 wt%) and MgO (∼ 4.5 wt%) content with Mg# ∼ 54, and exhibit magnesian, metaluminous characteristics of the Cordilleran granitoid-type formed in magmatic arc. The 2.87–2.86 Ga TTG gneisses are silica-rich (55–58 wt% SiO2), sodic (3–5 wt% Na2O, Na2O/K2O = 1–3), with HREE-depleted, and display the typical Archean medium- to low pressure TTG geochemical features groups. Their chemical compositions are characteristics of TTG-like melts derived from the partial melting of hydrated low- to high-K metabasic/thickened lower crust at various depths followed by magmatic differentiation during ascent. When compared to the TTG gneisses in the NGB, the ∼2.87 Ga granitic gneisses are K-rich, and high Gd/Yb, Th/Yb, Th/Nb, Sr/Y and La/Yb ratios but lower MgO, Yb, V, Y, Cr, Ni and Sr contents, matching typical Archean hybrid and potassic granitic rocks. We propose that the granitic gneisses were derived from the intra-crustal melting of a pre-existing felsic crust. The granitic and the TTG gneisses were generated contemporaneously through the same magmatic event at ∼2.87–2.86 Ga. The ∼2852 Ma monzogranitic gneisses are ferroan and metaluminous rocks, and show LREE enrichment with strongly fractionated REE patterns and positive Eu anomalies. Geochemical features, together with the presence of ∼2.9 Ga-old inherited zircon grains are consistent with the remelting of Mesoarchean granitoids. Considering the petrogenetic, regional geological and geochronological data, the Mesoarchean granitoid magmatism of the Ntem Complex was likely generated via complex transitional geodynamic regimes involving subduction and accretion processes.

Geochemical variations of anatectic melts in response to changes of P–T–H2O conditions: Implication for the relationship between dehydration and hydration melting in the Himalayan orogen

The anatectic mechanism is the most fundamental criterion in determining the petrogenetic relationship between migmatite, granulite and granite at convergent plate margins. Although two main anatectic mechanisms, namely water-absent (dehydration) and water-fluxed (hydration) melting, have been identified in many collisional orogens, their spatiotemporal relationship and genetic connection remain obscure. To address this issue, we conduct an integrated study of forward phase equilibrium and trace element modelling for partial melting of metapelite in the Himalayan orogen. The results are used to decipher changes of phase relation and melt composition in response to changes of temperature, pressure and water content. Pressure and water content mainly affect the solidus and evolving residual mineral assemblages, whereas temperature controls the anatectic reaction. Hydration melting at lower pressure and temperature would produce anatectic melts with relatively high SiO2, FeOT + MgO, CaO, K2O, and Ba contents and SiO2/Al2O3 ratios, but low Al2O3 and Na2O contents and Na2O/K2O and Rb/Sr ratios. In contrast, dehydration melting at higher pressure and temperature would generate anatectic melts with relatively high Al2O3 and Na2O contents and Na2O/K2O and Rb/Sr ratios, but low SiO2, FeOT + MgO, CaO, K2O, and Ba contents and SiO2/Al2O3 ratios. A comparison of geochemical compositions between the modelled melts and the two groups of well-characterized leucogranites in the Himalayan orogen indicates that the coeval dehydration and hydration melting would likely occur at the deeper and shallower crustal levels, respectively. In combination with the secular evolution of metamorphic facies series in the Himalayan orogen, we propose a spatiotemporally coupled dehydration-hydration melting mechanism. The early metamorphism at lower geothermal gradients would result in metamorphic dehydration in the lower crust and hydration in the upper crust during the syn-collisional period in the Early Cenozoic. As a result, the later metamorphism at higher geothermal gradients would lead to dehydration melting in the lower crust and hydration melting in the upper crust during the post-collisional period in the Late Cenozoic. This study highlights the applicability of phase equilibrium and trace element modelling to reveal the geochemical variations of anatectic melts in response to changes of P–T–H2O conditions. This provides new insights into the relationship between dehydration and hydration melting in collisional orogens.

Effect of Main Composition on the Viscosity and Thermal Stability of BaO-Containing Slag

The authors of this study systematically investigate the influence of the main components of BaO-containing slag on its viscosity and thermal stability. The results indicate that the viscosity of slag significantly increases with the mass fraction of the crystalline phase. Increasing the slag basicity from 1.00 to 1.10 and the MgO content from 5.0% to 9.5% is an effective way to weaken the influence of crystallization on slag viscosity and improve the stability of BaO-containing slag. Al2O3 content over 11% is necessary to maintain a higher slag temperature, which enhances the ability of BaO-containing slag to resist the influence of crystallization on relative viscosity. When the heat of BaO slag is greatly reduced, increasing the slag basicity from 1.05 to 1.15 and MgO content to over 6.5% can help maintain the thermal stability of slag. The effect of Al2O3 content on the viscosity of slag under conditions of fixed heat is greater than that under constant temperature conditions. As the heat decreases, the Al2O3 content increase from 9% to 13% has a more significant effect on the viscosity and temperature of slag. A lower Al2O3 content in slag is advantageous for reducing the influence of heat fluctuation on slag viscosity.

Chronolgy and Geochemistry of the Sijiaying Iron Deposit in Eastern Hebei Province, North China Craton: Implications for the Genesis of High-Grade Iron Ores

The Sijiaying iron deposit is located in the Eastern Hebei area of the southern section of the northern margin of the North China Craton (NCC) and is the largest single iron deposit in China. The deposit contains many banded iron formations (BIFs) and was proven to have more than 3 million tons of high-grade iron ore resources. This study carried out geochemistry and zircon U–Pb analysis of normal-grade iron ore, high-grade iron ore, and wall rock (biotite–leptynite, chlorite–sericite schist) in the Sijiaying deposit and discussed the genesis and metallogenic age of high-grade iron ore. BIFs have low concentrations of Al2O3 and TiO2 and high field strength element (HFSE) depletion, indicating almost no contamination via terrestrial debris. The standardized post-Archean Australian shale (PAAS) rare earth element (REE) distribution pattern indicates that the iron formation exhibits positive Eu, Y, and heavy rare earth element (HREE) anomalies and lacks negative Ce anomalies, indicating that the Sijiaying BIF was enriched with iron sources via high-temperature hydrothermal fluids from the seabed and deposited in an anoxic ancient marine environment. In addition, geological field work identified two types of high-grade iron ore in the mining area: primitive sedimentary and hydrothermally altered high-grade iron ore. Further ore geochemical research showed that the primitive sedimentary-type iron ore is similar in geochemistry to the BIF. In addition to low Eu/Eu* values, the hydrothermally altered high-grade iron ore shows geochemical characteristics similar to those of the BIF, suggesting that they share the same iron source but did not form at the same time. The total large ion lithophile element (LILE) (Sr, Ba, Pb) contents in primitive sedimentary-type high-grade iron ore are higher than those in hydrothermally altered high-grade iron ore, indicating that LILEs are carried away via fluids during the hydrothermal alteration process in normal-grade iron ore. The geochemical characteristics of biotite–leptynite and chlorite–sericite schist include high contents of SiO2 and Al2O3, light rare earth elements (LREEs), LILE enrichment (Rb, Ba, Sr, Zr), and HFSE depletion (Nb, Ta, P, Ti), characteristics that are similar to island arc volcanic rocks. The reconstruction of the original rock indicates that the wall rock is a product of volcanic sedimentary cycles in an island arc setting. Zircon cathodoluminescence images and LA–ICP–MS zircon U–Pb dating can be divided into four age groups (3283 Ma, 2547 Ma, 2500 Ma, and 2407 Ma), which correspond to the earliest volcanic activity in eastern Hebei, the main mineralization age of the Sijiaying BIF (the mineralization age of primitive sedimentary high-grade iron ore), a regional tectonic–metamorphic event, and the occurrence of migmatization (the mineralization age of hydrothermally altered high-grade iron ore), respectively. Therefore, the Sijiaying BIF and primitive sedimentary high-grade iron ores were deposited and mineralized at 2547 Ma, and the iron orebody was later altered via the hydrothermal solution at 2407 Ma, forming large-scale high-grade iron ores.

Geochemistry of granulite facies BIFs from the Luis Alves Craton (Southern Brazil): Implications for Archean-Paleoproterozoic depositional and tectonic settings

Banded Iron Formations (BIF) developed strongly during the Neoarchean – Paleoproterozoic Eras linked with global environmental processes such as the Great Oxidation Event (GOE) and changes in geodynamics, sea level, geobiology, hydrothermal systems, and sediment deposition conditions. BIF development and distribution worldwide are also related to supercontinent cycles, being a powerful tool to understand the evolution of plate tectonics. In this paper, we used field-based geological-structural data, petrography, X-ray diffraction, and lithogeochemical analyses to perform the first characterization of Banded Iron Formations at the Luis Alves Craton (LAC), Southern Brazil. The LAC BIF are classified as oxide and silicate facies, both with granoblastic texture. Oxide facies consists of quartz and magnetite. Besides these minerals, silicate facies contains olivine and ferrosilite, evidencing granulite metamorphism. Based on major elements oxide facies has a hydrothermal signature, with low content of Al2O3 and TiO2, whereas silicate facies register a continental sediment contribution been more enriched in these elements, MgO, MnO, and CaO. Trace-elements also indicate the main source for both silicate and oxide facies, which is seawater with a major influence of low-T hydrothermal sources, besides continental sedimentation sources. The Ce/Ce × anomaly is true negative, representing oxidizing waters, which also may represent a shallow water column depth. The depositional environment is inferred as a shallow, restricted basin. Oxide facies represents sedimentation closer to hydrothermal vents and with weak influence from continental clastic sedimentation, while silicate facies represent sedimentation closer to an adjoining continental landmass. Oxide facies has more Algoma-like characteristics, such as higher Fe and Eu contents, Sm/Yb and Eu/Sm typical of higher hydrothermal fluid inputs, and low siliciclastic contribution. On the other hand, silicate facies resembles Superior-type BIF, with higher siliciclastic contribution, negative Ce/Ce × anomalies, and Eu/Eu* <1.8. In summary, we propose the LAC BIF is representative of a transitional environment from Algoma-to Superior-type. The first depositions of the LAC BIFs may have developed within an Algoma-like environment during the Neoarchean. The waning tectonic and volcanic activity during the Siderian shifted to a platformal environment, with shallower waters that may induce the deposition of carbonates typical of Superior-type deposits. The depositional basin may have been closed by the Rhyacian and those sediments were then pushed down to the lower crust and underwent granulite facies metamorphism.

Nanoscale hydrous silicate melt inclusions at the clinopyroxene-amphibole interface in a mantle xenolith from the Perșani Mountains Volcanic Field

We studied amphibole lamellae and associated hydrous nano-silicate melt inclusions (NSMI) in upper mantle xenoliths from the Perșani Mountains Volcanic Field, southeastern Transylvania (Romania). Transmission Electron Microscope (TEM) results revealed submicron-scale pieces of evidence of escaped fluids in the form of nano-silicate melt inclusions along clinopyroxene-amphibole interfaces. These NSMIs consist of ∼80 vol% silicate glass and ∼ 20 vol% volatile bubble from which the former has a high SiO2 (>60 wt%) and Al2O3 (>20 wt%) and low CaO, FeO and MgO (<8 wt%) content determined by SDD-EDS analyses. We calculated the original bulk composition of the nano-silicate melt inclusions with Monte Carlo simulation, using hydrated fluid molecules and suggest that originally the nano-silicate melt inclusions had most probably low SiO2 (∼ 43.6 wt%) and high Al2O3 (∼ 15.5 wt%), Na2O (∼11.9 wt%) and H2O (∼ 30.3 wt%) contents. Using petrographic evidence, we propose that the amphibole lamellae formed as a result of post-entrapment reaction between clinopyroxene and the trapped fluid of the fluid inclusion. The presence of the hydrous nano-silicate melt inclusions suggest fluid migration along the clinopyroxene-amphibole interface, supporting the continuous growth of the studied amphibole. The association of the studied amphibole with hydrous nano-silicate melt inclusions suggests that H2O consumption from the fluid found in the micrometer-scale fluid inclusion continued at the nanoscale after a metasomatic event in the lithospheric mantle. This nanoscale process may also give information about the behavior of H2O globally in the lithospheric mantle where amphibole is stable, and along the lithosphere-asthenosphere boundary in younger oceanic and continental plates.

Zircon U–Pb Dating and Geochemical Characteristics of Chahannuo Gabbros in the Northern Margin of Qaidam Basin, Northern Tibetan Plateau

Late Paleozoic–early Mesozoic intrusive rocks are distributed widely along the northern margin of the Qaidam Basin in the northern Tibetan Plateau. To constrain the tectonic evolution, we carried out petrological, chronological, and geochemical studies of the Chahannuo gabbros. LA-ICP-MS Zircon U–Pb dating yields an age of 255.0 ± 0.9 Ma for the gabbros, which confirms the existence of Indosinian tectono-magmatic activity on the northern margin of the Qaidam Basin. The Chahannuo gabbros have low whole-rock SiO2, Fe2O3 contents, and high Al2O3 contents, which suggests a calc-alkaline affinity. In addition, the gabbros have high MgO, Cr, and Ni contents and Mg#, similar to those predicted of the regional basaltic melts, and indicating that they were affected mainly by fluid from the subducted slab. The Chahannuo gabbros are characterized by arc-like trace element patterns, with enrichment in LREE and LILE, and depletion in HREE and HFSE. No obvious negative Eu anomalies also indicate that no significant magmatic differentiation has occurred. The low Nb/La ratio and Ti content in gabbros samples suggests that the Chahannuo gabbros were partially contaminated by the crust during their formation. The Chahannuo gabbros have high incompatible element ratios (Rb/Sr, Th/Nd, and Th/La), which are closer to the category of enriched mantle. Combing our data with previous data from contemporaneous magmatism in the region, we suggest that the Chahannuo gabbros formed in a continental arc environment related to the northward subduction of the Paleo-Tethyan oceanic plate.

Fe-Si-C isotope constraints on the genesis of iron ores in Gongchangling iron deposit in northeastern China

The Gongchangling iron deposit is an oxide-facies Algoma-type banded iron formation (BIF) and one of the most representative iron deposits in northeastern China. We present new data from petrological, whole-rock geochemical, and Fe-Si-O isotope compositional data from the Gongchangling BIFs to constrain the origin of ore-forming materials and mineralization processes. The low Al2O3 and TiO2 contents in iron ores indicate that the sources of the BIFs were not contaminated by terrigenous clastic sediments. The Gongchangling BIFs are characterized by depletions in LREEs and 30Si and enrichments in HREEs, with positive Eu and Y anomalies. Given these and the Fe isotope results, we conclude that both high-temperature hydrothermal fluid and seawater contributed to the formation of the BIFs and that a mixture of seawater and ~ 0.1 % hydrothermal fluid, which percolated and dissolved the submarine volcanic rocks, provided the ore-forming materials. Combining the Ce anomalies, enrichments in heavy Fe isotopes and low δ13C compositions, we conclude that the fO2 of Archean seawater was limited. Integrated petrographic and geochemical evidence indicates that the high-grade iron ores from the Gongchangling BIFs experienced incomplete oxidation and low amounts of Fe precipitation in a marine environment and that dissimilatory iron reduction and metamorphic hydrothermal fluid played important roles.

Environmentally friendly and efficient green recovery of fluoride from waste aluminum electrolytic sediment using Al2O3

Green and efficient recovery of solid waste from aluminum electrolysis is of great significance. In this study, the sediment generated by aluminum electrolysis at the bottom of the waste tank was used as an alternative F resource. A new process of low-temperature acidification roasting with Al2O3 as the catalyst was performed to effectively recover F. The results of the single-factor experiment showed that a long reaction time and high acid-material ratio were conducive to improving the extraction rate of F. Under the conditions of 275 °C and 5 doses of sulfuric acid, the optimum F extraction rate was realized by roasting for 4 h with 1 dose of Al2O3 as the catalyst. The results of the XRD, SEM and chemical analyses showed that NaAl(SO4)2 was the main component produced in the calcination reaction using Al2O3 as the catalyst, rather than NaHSO4 (produced in the calcination process without a catalyst). This ensured complete combination of H and F, which greatly improved the extraction rate of F (from 80.76 to 99.76%). The proposed mechanism can provide not only an optimization scheme for the roasting of waste sediment at the furnace bottom, but also a more effective recovery treatment for the acidification roasting of other solid wastes with low Al2O3 content.