Homogenization Temperatures Research Articles

Genesis of the Bailugou Vein-Type Zinc-Lead-Silver Deposit, Eastern Qinling Orogen, China: Constraints from Ore Geology and Fluid Inclusions

The Bailugou vein-type zinc-lead-silver deposit is located in the Eastern Qinling Orogen, China. There has been a long-standing debate about whether its formation is related to magmatism or metamorphism. To determine the origin of ore-forming materials and fluids, we conducted a geological and fluid inclusion investigation of the Bailugou. Field surveys show that the vein-type orebodies are controlled by faults in the dolomitic marbles of the Mesoproterozoic Guandaokou Group, and they are distal to the regional Yanshanian intrusions. Four ore stages, i.e., quartz–pyrite ± sphalerite (Stage 1), quartz–polymetallic sulfides (Stage 2), dolomite–polymetallic sulfides (Stage 3), and calcite (Stage 4), are identified through microscopic observation. The homogenization temperatures of measured fluid inclusions vary in the range of 100 °C to 400 °C, with the dominating concentration at 350 °C to 400 °C, displaying a descending trend from early to late stages. The estimated formation depth of the Bailugou deposit varies from 2 km to 12 km, which is deeper than the metallogenic limit of the epithermal hydrothermal deposit but conforms to the typical characteristics of a fault-controlled deposit. The ore-forming fluid in Stage 1 originates from a fluid mixture and experiences a phase separation (or fluid immiscibility) between the metamorphic-sourced fluid and the fluids associated with ore-bearing carbonate-shale-chert association (CSC) strata. This process results in the transition to metamorphic hydrothermal fluid due to water–rock interactions in Stage 2, culminating in gradual weakening and potential fluid boiling during the mineralization of Stage 3. Collectively, the Bailugou lead-zinc-silver mineralization resembles an orogenic-type deposit formed by metamorphic fluids in the Qinling Yanshanian intracontinental orogeny.

Formation of the intrusion-hosted orogenic-type gold lodes: Exemplified by the Axile gold deposit in the Chinese Altai

Unlike the gold deposits typically hosted in metamorphosed volcanic-sedimentary sequences, the recently discovered Axile gold deposit (over 13 t Au at 5.35 g/t) is a unique example in the Chinese Altai for evaluating the genesis of intrusion-hosted lode gold deposits in metamorphic terranes. The orebodies in this deposit occur as quartz veins and altered tectonites hosted in the sinistrally sheared quartz diorite and biotite granite zones in the Habahe intrusion. The quartz vein-type ores are composed of quartz-pyrite veins and quartz-polymetallic sulfide veins, in which gold-tellurides also occur. The altered tectonites, spatially associated with the quartz veins, are composed of deformed and altered rocks of quartz diorite and biotite granite. Main alterations include quartz, sericite, calcite, chlorite, albite, pyrite, chalcopyrite, and gold-tellurides. Two types of fluid inclusions are identified in the ores, i.e., (1) carbonic-aqueous (C-type) and (2) aqueous (W-type), with the C-type being dominated. These fluid inclusions yield salinity ranging from 3.6 to 9.0 wt% NaCl equivalent and homogenization temperatures in the range of 249 − 387 ℃, suggesting a typical mesothermal NaCl-CO2-H2O system. The Axile deposit thus corresponds to an orogenic-type gold deposit.The hydrothermal titanites in the auriferous quartz-pyrite veins yield in situ U-Pb ages around 278.4 ± 2.4 Ma (MSWD = 3.1, 2σ), which constrain the gold mineralization timing as Permian. The mineralized quartz diorite and biotite granite yield zircon U-Pb ages of 377.0 ± 1.0 Ma (MSWD = 0.1; 1σ) and 394.0 ± 1.2 Ma (MSWD = 0.4; 1σ), respectively, which show that the ore-hosting intrusions were emplaced in the Devonian, obviously earlier than the gold mineralization. The light δ13CV-PDB values (−15.5 ‰ to −6.7 ‰, average −10.7 ‰) of the CO2 extracted from the fluid inclusions display a significant contribution from the organic carbon in sediments. Given the sedimentary rocks underwent Permian greenschist to amphibolite facies metamorphism in the Chinese Altai, accompanied by the synchronous structural deformation and shearing activities, it could be concluded that the Axile gold deposit is formed by a shear zone-controlled mesothermal system that originated from metamorphic-devolatilization. The Chinese Altai Orogen is an orogenic-type gold metallogenic belt, containing both the intrusion- and metamorphic rock-hosted gold deposits, illustrated by a consistent genetic model.

Impact of temperature on sphalerite chemistry: Simulation experiments of sphalerite in MVT Zn-Pb sulfide deposits in the Beiba Dome, northern Sichuan Basin, China

Many sedimentary metal deposits are rich in organic matter, and some organic deposits are metal deposits themselves. These metal deposits, represented by MVT Zn-Pb deposits, are widely distributed in the world, and their industrial types (Pb + Zn > 5 %) are also very rich, which has important theoretical and economic significance. However, there is no systematic research on the metallogenic mechanism of MVT Zn-Pb deposits in the participating organic matter. Therefore, geochemical simulation experiments and thermodynamic calculations have been used to examine the role of organic matter in reconstructing the ore-forming process of MVT Zn-Pb sulfide deposits. Additionally, the precipitation chemistry of sphalerite under the mineralization process mediated by organic matter is explained. Guided by the evidence on the homogenization temperature of fluid inclusion, the temperature range, from 60 °C to 200 °C, has drawn a close relationship between the temperature and the ore-forming mechanism. Notably, this reflects sphalerite’s chemical composition and morphology, even assisting in interpreting its chemical formation. The results showed that 80 °C is the beginning temperature for ZnS formation calculated from the inductively coupled plasma mass spectrometry analysis (ICP-MS) under the precipitation simulation experiments with the participation of organic matter. With the increased temperature, the rate of ZnS formation showed a trend of rapid growth in the early stage (80–140 °C) and relatively slow in the later stage (160–200 °C). This finding suggests a closer coupling relationship between metal mineralization and the maturation-genesis of organic matter, mainly the formation of the ancient oil reservoir. Following the continued increase in temperature, the morphology of ZnS was significantly different from that of the scanning electron microscope (SEM), with an apparent fine granular structure at high temperature. Likewise, more ZnO was also found through the X-ray photoelectron spectroscopy analysis (XPS), reducing the purity of the ZnS in sphalerite. Thus, this study helps reveal the metallogenic mechanism of MVT Zn-Pb sulfide deposits from the viewpoint of sphalerite chemistry under the participation of organic matter from temperature change. Furthermore, it provides a valuable theoretical and experimental basis for the later prospecting of the metal deposits.

Numerical simulation of a base metal deposit related to a fossil geothermal system

Fossil and active geothermal systems that produce ore deposits are sites of complex physicochemical processes and a favorable combination of factors related to the amount of metal-bearing fluid that flows through the system, ore fluid metal concentrations, depositional efficiency, and the duration of ore deposition. Of all these factors, the length of the mineralizing event is one of the least understood aspects of ore genesis.We used fluid inclusion data, chemical compositions of base metal sulfides, and fluid flow rates to constrain a reactive-transport model of a fossil geothermal system - the Patricia Zn-Pb-Ag deposit in northern Chile. The Patricia deposit consists of quartz and base metal sulfide veins of hydrothermal origin with structural control, hosted in a volcanic succession with intense propylitic alteration. The fluid inclusions are liquid-rich, with homogenization temperatures ranging from 250 to 150 °C and salinities between 22 and 1 wt% NaCl equiv., with an early fluid mixing trend and no evidence of boiling in the system. Sulfide mineralogy indicates intermediate sulfidation conditions.To identify the most relevant geochemical and transport parameters controlling the formation of this fossil geothermal system >1000 simulations were performed using the reactive-transport code TOUGHREACT. The paragenesis of the deposit is mimicked by a model of successive stages of fluid circulation consistent with the observed mineral assemblage distribution, the fluid inclusion data, and the estimated resources in the deposit.The entire geothermal activity of the system was modeled considering 10,000 years of fluid-rock interaction, with periods of circulation of metal-barren fluids followed by metal-rich fluids driving the ore formation. In the initial model, base metal solubility with predominant chloride complexing suggests that the most efficient ore-forming mechanism for the Patricia deposit was the result of the interaction of two different fluids, one fluid transporting metals and another fluid transporting reduced sulfur, mixing in a rock volume of high permeability. Mass balance estimations with this model give a period of 3500 to 5000 years for the ore stage duration in which all the ore resources of the Patricia deposit could have been precipitated by fluid mixing.In a second model, the previous estimates for the duration of the main ore stage were used to simulate the fluid-rock interaction during the ore stage for 3500 years. The results indicated the importance of the permeability of the host rock enhanced by fractures to concentrate the volume of the mineralization and the role of the hydrothermal alteration assemblage in controlling the circulating fluid acidity. A higher efficiency in forming sulfide minerals appears to coincide with pH values ranging from 5.1 to 5.3.The results of both models are validated by replicating the system evolution, reproducing the same mineral alteration assemblage, the expected base metal resource distribution, and similar amounts of ore resources to those of the Patricia deposit: a total of 52,602 tons of lead and 157,731 tons of zinc. The models indicate that the hydrothermal event might be two times longer than the ore stage.

Genesis of the Mamuniyeh copper deposit in the central Urumieh-Dokhtar Magmatic Arc, Iran: Constraints from geology, geochemistry, fluid inclusions, and H–O–S isotopes

The Mamuniyeh Cu deposit is located in the central part of the Urumieh-Dokhtar Magmatic Arc (UDMA), 10 km south of the city of Mamuniyeh, Iran. Mineralization is controlled by faults with a NW-SE trend and hosted within an Eocene volcanic sequence and Oligo-Miocene hypabyssal calc-alkaline monzonitic and gabbroic bodies. Quartz + chalcopyrite veins are most abundant and high-grade ore containing up to 5 wt% Cu, although quartz + pyrite veins have the most abundant sulphide content. In addition, quartz + chalcopyrite + specular hematite ± pyrite veins/veinlets are another common mineralized assemblage in the Mamuniyeh copper deposit, with pyrite, chalcopyrite, bornite, and oxide minerals (specular hematite, titanomagnetite, and magnetite) typical of the hypogene stage. Chalcocite, covellite, and dignite also formed at the margins of primary sulphides in the supergene (paleoweathering) stage. The mineralized veins exhibit colloform, crustiform, open space-fillings, replacements, and dissemination textural characteristics associated with mineralizing assemblages with silicification, argillization, chloritization, and sericitization assemblages. The salinity for L > V fluid inclusions is between 1.74 to 11.7 wt% NaCl and for (V > L) inclusions between 1.7 to 11.4 wt% NaCl. The average homogenization temperature and salinity for quartz + chalcopyrite + pyrite veins is 186 °C and 4.9 wt% NaCl. In the quartz + chalcopyrite assemblage an average of 185 °C and 4.5 wt% NaCl and for quartz + chalcopyrite + specularite ± pyrite (QCSP) an average of 195 °C and 5.59 wt% NaCl was determined. In these three vein types, the fluid density has almost identical values ranging from 0.8 to 1.0 g/cm3. The mineralizing system evolved in two-stages; the first metal precipitation occurred at less than 1 km of crustal depths and second metal deposition stage at shallower crustal levels (less than 500 m). Although it appears that the boiling process occurred within the fluids of the area, the primary factor contributing to Cu mineralization was influenced by fluidmixing processes. The δ18O and δD values of ore fluids computed vary from + 6.08 to −0.50 ‰ and −92 to −71 ‰, respectively, indicative of the blending of oxidizing and cooler meteoric waters with primary magmatic fluids. Calculated values of δ34S of H2S in equilibrium with chalcopyrite ranges from −7.6 to −1.9 ‰ and H2S in equilibrium with pyrite ranges from −7.1 to −3.8 ‰, respectively; this is consistent with monzodiorite to gabbro as the magmatic sulphur source for copper mineralizing fluids. Furthermore, the QCSP vein data align more closely with primary magmatic water compared to other veins, suggesting that precipitation occurred mainly from magmatic fluids, which experienced depletion in δ18O due to mixing with meteoric waters (shallow oxygenated ground waters), which caused sulphide deposition. The geochemical features for these magmas show that contamination with crustal materials occurred during the ascent of the parent magma, as well as the role of suprasubduction fluids released from the subducting plate in mantle metasomatism. Based on all evidence, Cu mineralization in the Mamuniyeh deposit has been categorized as a low-sulphidation epithermal-type system, which formed during active magmatism in the central part of UDMA.

Improvements in Injection Moulds Cooling and Manufacturing Efficiency Achieved by Wire Arc Additive Manufacturing Using Conformal Cooling Concept.

The plastic injection moulding industry is a constantly developing industrial field. This industrial process requires the manufacturing of metal moulds using complex heating and cooling systems. The purpose of this research is to optimize both the plastic injection moulding process and the mould manufacturing process itself by combining practices in this industry with current additive manufacturing technologies, specifically Wire Arc Additive Manufacturing (WAAM) technology. A mould punch was manufactured by using both WAAM technology, whose internal cooling system has been designed under the concept of Conformal Cooling, and conventional cooling channel designs and manufacturing techniques in order to carry out a comparative analysis. Theoretical results obtained by CAE methods showed an improvement in heat extraction in the WAAM mould. In addition, the WAAM mould was able to achieve better temperature homogeneity in the final part, minimizing deformations in the final part after extraction. Finally, the WAAM manufacturing process was proven to be more efficient in terms of material consumption than the conventional mould, reducing the buy-to-fly ratio of the part by 5.11.

An experimental and comparative study on passive and active PCM cooling of a battery with/out copper mesh and investigation of PCM mixtures

The carbon emission contribution to global warming accelerated both research on and transition to electric vehicles (EVs). Drivers demand high power, fast acceleration and less charging times. All these demands require high C rate charging/discharging demands from batteries. The rate of heat generation is exponentially proportional to C rates which decreases battery lifetime and may lead to thermal runaway. However, a battery thermal management system decreases thermal runaway risk and decelerates battery degradation via controlling battery temperature. In this paper, we first document the thermal conductivity enhancement via copper foam into phase change material (PCM) domain to uncover their possible use in EV thermal management applications. Maximum 15.93 times increment is achieved with a specific copper foam. Then, physical properties and behaviors of distinct PCM mixtures are documented. Homogeneity of mixtures is associated with the chemistry of PCMs and the mixture melting point is proportional to the volume weighted average of melting temperatures. The results document that the PCM with relatively lower melting point is beneficial when end of discharge temperatures considered, except for high discharge rate of 2C. Temperature uniformity across the battery increases with relatively higher melting point PCM. Experiments also document that the amount of PCM volume lost via insertion of copper foam yields higher end of discharge temperatures. Overall, both PCM and copper foam enhances temperature homogeneity and their benefit becomes more sensible during drive cycles relative to continuous charge/discharge use cases.

Magma Degassing andGoldMineralizationinthe Alkaline Intrusion- HostedGiltEdgeGoldDeposit,NorthernBlackHills, SouthDakota,USA

Gold mineralization in the Gilt Edge deposit was closely associated with magmatic differentiation and the formation of a Tertiary alkaline intrusive complex within the Lead–Deadwood dome.. Fluid inclusions and trace element geochemistry were used to study fluid evolution and determine sources. Quartz disseminated in unaltered trachyte porphyry hosts two populations of primary inclusions: 1) hypersaline i S–L–V a red hematite crystal and 2) mixtures of L–V and V– L that record phase separation at ~700oC. Whereas samples of hydrothermal quartz collected from in ore zones within and beyond structures (e.g., fault and breccia zones) contain dominant populations of V–L and L–V inclusions, respectively. Mineralization in structures formed from complex fluids of magmatic origin based on inclusions containing five transparent salt crystals and opaque crystals with cubic and round habits that have homogenization temperatures (Th) 650oC and salinities 63 wt.% NaCl equiv. In contrast, broader areas of disseminated mineralization in argillized and propylitized rocks contain hydrothermal quartz hosting large populations of L–V inclusions with Th of 200o360oC and salinities of 10–30 wt.% NaCl equiv., which reflect fluid mixing. Trace element concentrations are significantly higher in samples from structures and define zones of near surface Ag–As–Zn–Pb and deep Au–W–Mo–Cu. Whereas low trace element concentrations characterize propylitized quartz trachyte porphyry, except for high concentrations of Sb and Hg that occur at depth and likely track the retreat of isotherms as the hydrothermal system collapsed. These data show that during differentiation in a deep magma chamber, volatile-rich low-density fluids were periodically degassed into preexisting structures that were reactivated. Gold deposition during four stages of mineralization likely occurred due to boiling, changes in oxygen fugacity, and fluid mixing.

Source of Ore-Forming Fluids and Ore Genesis of the Batailing Au Deposit, Central Jilin Province, Northeast China: Constraints from Fluid Inclusions and H-O-C-S-Pb Isotopes

The Batailing Au deposit is a vein-type deposit in central Jilin Province, situated in the southern sector of the Lesser Xing’an–Zhangguangcai Range within the eastern Central Asian Orogenic Belt. NE-trending fault-controlled orebodies occur in the Upper Permian Yangjiagou Formation and quartz diorite–porphyrite. The mineralisation process was delineated into three stages: (I) quartz–arsenopyrite–pyrite, (II) quartz–polymetallic sulphides (main Au mineralisation stage), and (III) quartz–pyrite–carbonate. Fluid inclusions (FIs) in quartz were identified as four types: PC-type (pure CO2), C1-type (CO2-bearing), C2-type (CO2-rich), and W-type (aqueous two-phase). Raman spectroscopy analysis revealed that the vapor components of the FIs predominantly comprised CO2 with minor quantities of CH4 in stages I–II. Stages I and II encompassed four types of FIs with homogenisation temperature ranging from 264 to 332 °C and 213 to 292 °C and salinity spanning from 4.7 to 11.2 wt% and 1.8 to 11.6 wt%, respectively. Stage III exclusively contained W-type FIs with homogenisation temperature ranging from 152 to 215 °C and salinity spanning from 1.4 to 6.4 wt%. H-O isotopic values (δD = −84 to −79.6‰, δ18OH2O = 6.2 to 6.4‰ in stage I and δD = −96.4 to −90.4‰, δ18OH2O = 2.8 to 4.4‰ in stage II) and microthermometric data indicated that the ore-forming fluids are initially from a magmatic source, with later meteoric water input. Low C isotopic data from CO2 in FIs in quartz (−24.4 to −24.3‰ in stage I and −23.7 to −22.6‰ in stage II) indicated an organic carbon source. Ore precipitation is mainly attributable to fluid immiscibility. S-Pb isotopic data (δ34S = −3.5 to −1.6‰; 206Pb/204Pb = 18.325–18.362, 207Pb/204Pb = 15.523–5.562, 208Pb/204Pb = 38.064–38.221) revealed that ore metals primarily originated from magma. Based on this research, the origin of the Batailing Au deposit is of the mesothermal magmatic–hydrothermal lode type.

Phase Composition of AlTiNbMoV, AlTiNbTaZr and AlTiNbMoCr Refractory Complex Concentrated Alloys: A Correlation of Predictions and Experiment

Designing complex concentrated alloys (CCA), also known as high entropy alloys (HEA), requires reliable and accessible thermodynamic predictions due to vast space of possible compositions. Numerous semiempirical parameters have been developed for phase predictions over the years. However, in this paper we show that none of these parameters is a robust indicator of phase content in various refractory CCA. CALPHAD proved to be a more powerful tool for phase predictions, however, the predictions face several limitations. AlTiNbMoV, AlTiNbTaZr and AlTiNbMoCr alloys were prepared using blended elemental powder metallurgy. Their phase and chemical composition were investigated by the means of scanning electron microscopy, energy-dispersive X-ray spectroscopy and X-ray diffraction. Apart from the minor contamination phases (Al2O3 and Ti(C,N,O)), AlTiNbMoV and AlTiNbMoCr exhibited single-phase solid solution microstructure at the homogenization temperature of 1400 °C, while Al3Zr5 based intermetallics were present in the AlTiNbTaZr alloy. None of the simple semiempirical parameter was able to predict phase content correctly in all three alloys. Predictions by CALPHAD (TCHEA4 database) were able to predict the phases with limited accuracy only. Critical limitation of the TCHEA4 database is that only binary and ternary phase diagrams are assessed and some more complex phases cannot be predicted.

Formation of the Lianhuashan Cu deposit in the southern Great Xing’an Range, NE China: Constraints from fluid inclusions, whole-rock geochemistry, zircon U–Pb geochronology, and H–O–S–Pb isotopes

The medium-sized Lianhuashan Cu sulfide deposit is located in the southern Xing’an Range of Inner Mongolia, NE China. The zoned massive sulfide vein ores are hosted mainly in the Permian Dashizhai Formation, and the ore veins are controlled by NW–NNW-trending structures. The ore-forming process comprises four stages: arsenopyrite–quartz (I); chalcopyrite–pyrite–quartz (II); pyrite–chalcopyrite–sphalerite–galena–quartz (III); and ore-barren sulfide–quartz–carbonate (IV). Three types of fluid inclusions (FIs), namely vapor-rich two-phase (LV-type), liquid-rich two-phase (VL-type), and daughter mineral-bearing three-phase (SL-type), are distinguished. Stage I, II and III contain all types of FIs (LV-, VL-, and SL-type), with homogenization temperatures (Th) of 268–462°C, 230–382°C and 180–340°C and salinities of 3.4–52.3, 3.4–44.5 and 3.7–39.9 wt% NaCl eqv., respectively, whereas stage IV has only VL-type FIs, with Th = 152–232°C and salinity = 3.4–7.9 wt%. Fluid geochemical data show that the Lianhuashan ore fluids were of medium–high temperature (236–382 °C), high-salinity (31.5–44.5 wt%), and relatively oxidizing conditions, typical of a NaCl-H2O system. The microthermometric and H–O isotope data (δ18OH2O = − 9.0 to 6.1 ‰; δD = − 149.0 to − 99.0 ‰) indicate that the ore fluids were initially magmatic with later meteoric water incursion. The sulfide S (δ34S = − 2.9–3.8 ‰) and Pb (206Pb/204Pb = 17.954 − 18.492, 207Pb/204Pb = 15.427 − 15.739, 208Pb/ 204Pb = 37.815 − 38.357) isotopes support that the metals were magmatic-derived. Fluid boiling, cooling, and meteoric water mixing were likely the main ore precipitation mechanism at Lianhuashan.We suggest that Cu minerals at Lianhuashan were precipitated with boiling at ∼ 1km depth. For the ore-forming granodiorite porphyry (zircon U-Pb age: 252.8 ± 1.8 Ma), geochemical data indicate that the primary magma was formed by partial melting of the thickened or delaminated lower crust. Integrating the available age, geological, and geochemical evidence, we suggest that mineralization at Lianhuashan is spatial–temporal and genetically associated with the granodiorite porphyry, and was formed in a volcanic arc setting after the Paleo-Asian Ocean closure.

Multistage fluid mixing events induced Sn polymetallic super-enrichment at Dulong in Yunnan Province, South China

Dulong Sn polymetallic deposit is a world-class skarn tin deposit situated at the Youjiang basin with a reserve of 0.4 Mt Sn at 0.56 %, 5.0 Mt Zn at 5.12 %, together with 7 kt In. The deposit predominantly occurs within the Neoproterozoic Xinzhaiyan Formation and is controlled by NS-trending faults. Based on elaborate field and petrographic observations, the Dulong Sn polymetallic deposit was divided into four mineralization stages: stage 1 (prograde stage), stage 2 (retrograde stage), stage 3 (quartz-sulfide stage) and stage 4 (carbonate stage). Tin mineralization primarily occurs as cassiterite during stage 2, with additional cassiterite-stannite formation noted in stage 3. Analysis of fluid inclusions across these stages reveals the evolutionary history of the mineralizing fluids and the precipitation mechanisms at Dulong. During stage 1, diopside hosts both daughter-bearing multiphase inclusions and vapor-rich inclusions. The daughter-bearing multiphase inclusions exhibit homogenization temperatures ranging from 510 to 574 °C and salinities between 44.7 and 49.6 wt% NaCl equiv., whereas the vapor-rich inclusions display homogenization temperatures of 573–586 °C and salinities from 2.9 to 4.0 wt% NaCl equiv., indicating a boiling fluid process. Cassiterite (stage 2) features primarily liquid-rich two-phase inclusions, with homogenization temperatures of 351–410 °C and salinities of 6.3–9.6 wt% NaCl equiv. These inclusions document the mixing of magmatic fluid with meteoric water, which is likely the principal mechanism driving initial tin mineralization. Similarly, the same type of inclusions is also recorded in cassiterite of stage 3. The homogenization temperature of the inclusions in cassiterite is 290–334 °C and the salinities of the inclusions is 3.4–8.4 wt% NaCl equiv. Comparatively, the temperature continued to decrease in stage 3, indicating that fluid mixing may have persisted during this stage which could also explain the occurrence of cassiterite and stannite in this stage. In addition, redox reaction where CO2 and/or As (III) serve as oxidants may also be another mechanism to exact cassiterite from ore-forming fluid. Our Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data suggests that cassiterite of the Dulong deposit involves a variety of complex substitutional mechanism. Due to the differing geochemical properties of the elements and variations in their concentrations, there is an indication that two phases distinct mineralizing fluids may have been present. The varying geochemical properties and concentrations of elements such as Nb, Ta, Zr, Fe, In, and Ga align with microthermometric results, indicating a reduction in magmatic hydrothermal fluid contribution and/or a transition from high to low temperatures in the hydrothermal system. This variation is also likely attributable to fluid mixing processes.

Fluid inclusion and pyrite geochemistry of the Jiapigou gold deposit, North China Craton: Implication for origin of orogenic gold deposit?

The Jiapigou auriferous belt in Jilin province has been recognized as substantial gold-producers in the North China Craton (NCC). Gold mineralization in this district mainly occurs in mineralized quartz veins and alteration zones, characterized by silicification, pyritization, and argillitization. The quartz veins contain three generations of mineralized quartz, namely, qtz1 (probably oldest), qtz2 (slightly younger), and qtz3 (probably youngest) were identified using SEM-CL. The fluid inclusions in all three generations of quartz are broadly of three types, viz., bi-phase Ia (H2O-CO2), tri-phase Ib (H2O-CO2-NaCl ± CH4), and II (H2O-NaCl).The micro-thermometric analysis of the type Ia and Ib fluid inclusion in qtz1 & qtz2 have aqueous-carbonic composition and exhibit a similar salinity of 1.1 to 7.8 wt% NaCl equivalent, whereas the homogenization temperature (Th) range varies from ∼237 to ∼350 °C. These ore-related fluid inclusions are of low to moderate salinity, and show mixture of CO2 and CH4. On the other hand, Type II fluid inclusions are dominant in qtz3. They have salinity of 3.2 to 12.7 wt% NaCl equivalent and homogenization temperature varying between 180 °C and 210 °C. These data indicate that the ore-forming fluid evolved from a CO2–H2O–NaCl ± CH4 system during the mineralization period.The X-ray elemental maps of pyrite acquired using electron microprobe analysis (EPMA) show irregular zones of Co and Ni indicating two generations of pyrite. The early-stage pyrite which occupies core portion shows high Co and Ni, whereas the later-stage pyrite occupying rim has lower Co and Ni. The laser ablation-inductively coupled plasma-mass spectrometer (LA-ICPMS) analyses of pyrite has indicated that pyrite-1 is rich in Au + Ag + Se + Cu + Co + Ni, whereas, pyrite-2 has lower concentration of these elements. A positive correlation between Fe and other chalcophile elements reported here (i.e. Au + Ag + Se + Cu + Co + Ni), might be due to fluid-rock interaction resulting into a saturated fluid that subsequently precipitated along the microfractures within earlier-formed pyrite and quartz. The in-situ δ34S values in pyrite from Jiapigou deposits overlap in the range of +4.5 to +9.6 ‰, which is consistent with the ore-forming fluids of the crustal origin input during fluid-rock interaction. The systematic pyrite compositional observations and fluid inclusions study documented here to provide new insight into the process of ore formation for the Au enrichment in the Jiapigou deposit

Coupled Effects of Paleofluid Evolution on Ultra-deep Microbialite Reservoir Modification: A case study of the upper Ediacaran Deng-2 Member within the Penglai area of central Sichuan Basin, SW China

Paleofluid-rock interaction results in the modification of the ultra-deep reservoir quality, but the coupling effects of the paleofluid evolution on reservoir quality modification are still underestimated. Here, the multi-stage dolomite cements have been studied by means of core observations, thin section identification, fluid inclusions, and in situ elements and isotopic analyses in order to reaveal the paleofluid evolution processes and their effects on the reservoir quality. The fibrous dolomite cement (FDC) and bladed dolomite cement (BDC) both have similar geochemical properties and homogenization temperature (Th) to the matrix dolostone. Subsequent early silicification occurs (QZ1). However, silt- to fine-sized crystalline dolomite cement (CD2) has higher concentration of Fe and medium rare earth element, more negative δ18O than for FDC and BDC, and 103.4 to 150.2 °C in Th. The first petroleum charge episode solid bitumen 1 (SB1) followed the CD2. The medium to coarse sized crystalline dolomite cement (CD3) is characterized by the higher Mn and lower Sr concentration than CD2, positive δEu anomaly, negative δ13C and δ18O, high 87Sr/86Sr ratio and 138.9 °C to 184.3 °C in Th. The solid bitumen 2 (SB2) occurs after CD3. Subsequently, the saddle dolomite (SD) has higher Fe and Mn concentration and lower Na and Sr than others cement, δEu positive anomaly, negative δ13C and δ18O, high 87Sr/86Sr ratio and 177.5 °C to 243.6 °C in Th. Eventually massive silicification (QZ2) took place. The FDC, BDC, QZ1 and SB1 formed in the early diagenetic stage and have little negative effect on the reservoir quality. But the CD2 and CD3 dramatically decreased the reservoir quality related to a quantity of hydrothermal fluids entrance in the mesodiagenetic stage along the strike-slip faults and the unconformity surface at top of the Deng-2 Member during the late stage of the Caledonian orogeny. The reservoir spaces were retained and enlarged during the late diagenetic stage when the peak petroleum charge occurred, massive silicification and thermochemical sulphate reduction took place with SB2, SD and QZ2 being formed. The research outcome may update our understanding on the retention mechanism and the insights for further hydrocarbon exploration of Precambrian ultra-deep microbial reservoirs.

Mechanism of homogenization temperature and time on Fe-containing phase transition in AA8014 aluminum alloy

The presence of coarse Fe-containing phases detrimentally affects the fracture toughness of 8xxx aluminum alloys, and their complete dissolution during homogenization is unattainable. Therefore, it is essential to determine the optimal homogenization temperature and time to facilitate particle breakup during hot rolling, necessitating the development of effective homogenization processes. This study systematically examines the effect of homogenization temperature and time on the transition of Fe-containing phases in AA8014 aluminum alloy using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The transition mechanisms of Fe-containing phases during homogenization were elucidated through first-principles calculations, thermodynamics, and kinetics calculations. Under homogenization conditions of 610–650 ℃/12 h and 630 ℃/1–20 h, the Al6(Fe,Mn) phase initially transforms into the α-Al12(Fe,Mn)3Si phase with a “micropore structure” via the reaction. Subsequently, the α-Al12(Fe,Mn)3Si phase transforms into the Al3(Fe,Mn) phase. First-principles calculations confirm the sequential stability enhancement of the Al6(Fe,Mn), α-Al12(Fe,Mn)3Si+6Al, and Al3(Fe,Mn) phases. Homogenization kinetics indicate an optimal homogenization time of 11.5 h at 630 ℃, rationalizing the observed phase transitions and homogenization treatment. This study provides a foundation for the manufacture of 8xxx series aluminum alloys.

Fluid evolution and genesis of the Shipenggou gold deposit in Central Jilin Province, China: Constraints from C–H–O and in–situ sulphur isotopes of pyrite and fluid inclusions

The origin and evolution of the Shipenggou gold deposit in the Shipenggou–Jiapigou–Jinchengdong (SJJ) gold belt in Jilin Province, Northeast China, remain poorly understood. In this study, fluid inclusion and C–H–O–S isotopes from the Shipenggou deposit were investigated to clarify the fluid evolution and mineralisation process. The gold mineralisation is hosted in the biotite plagiogneiss of the Archaean Sandaogou Formation and is dominated by gold–bearing quartz veins. The orebodies are controlled by NNE– and NEE–striking brittle–ductile structures. Four stages of mineralisation have been identified: (I) milky quartz–minor pyrite, (II) quartz–pyrite–minor gold, (III) gold–quartz–polymetallic sulphide, and (IV) quartz–carbonate. Fluid inclusions were identified as four types: aqueous (VL–type), CO2–bearing (CL–type), CO2–rich (LC–type), and carbonic (PC–type). VL–, CL–, LC–, and PC–type FIs were developed within quartz from Stages I–II. Stage III quartz contains both CL– and VL–type FIs. Only VL–type FIs were observed in calcite from Stage IV. The total homogenisation temperatures (Tht) of FIs in Stages I, II, III, and IV are of 281.5–324.8, 215.5–269.1, 151.2–198.3, and 125.4–149.5 °C with salinities of 2.8–13.2, 2.8–9.6, 3.2–8.4, and 3.0–5.9 wt% NaCl eqv. Laser Raman spectroscopy analysis indicated the CL– and PC–type FIs from Stages I and II contain CO2 and minor quantities of CH4. The ore–forming fluids have developed from a medium temperature, low–medium salinity immiscible NaCl–H2O–CO2 ± CH4 system to a low temperature, low salinity homogeneous NaCl–H2O system. The HO isotopic compositions indicate that the initial ore–forming fluids were mantle–derived magmatic water. Subsequently, the ore–forming fluids were gradually joined by meteoric water. δ13C values indicate C in the fluids have originated from organic matter. Organic matter may have originated from the mantle, which mixed crust materials influenced by the subduction of the Palaeo–Pacific slab. In–situ, S isotope data of pyrite indicate that the origin of sulphur at the Shipenggou deposit is the mantle containing a crust component. Based on the above analysis results, the Shipenggou gold deposit is a mesothermal magma-hydrothermal vein–type gold deposit.

Microtectonics and fluid evolution in the Katanga Supergroup (Tenke Fungurume Mining District): Evidence of pre- to post-orogenic Cu-Co mineralization in the Central Africa Copperbelt

The sediment-hosted stratiform copper-cobalt deposits in the Central African Copperbelt (CACB) are renowned for their resource potential, encompassing Cu-Co (Ni, U) and Cu-Zn-Pb (Ag, Ge, Mo, Cd) mineralization. Microstructural and microthermometric analyses of carbonate-quartz veins from the Tenke Fungurume mining district, situated in the central part of the Katanga Copperbelt (KCB), have delineated a pre- to post-folding paragenesis of vein formation and hypogene Cu-Co ore mineralization. The mineralization primarily consists of chalcopyrite, chalcocite, carrollite, and bornite.Pre-folding veins comprise bedding-normal veins related to the extension stage, occasionally linked with mullion development during the following compressional stage, as well as bedding-parallel beef veins. Syn-folding mineralization manifests as saddle reef veins within fold hinge zones, fracture-filling veins aligned with tangential longitudinal strain in hinge zones of folded bedding-parallel veins, thin veinlets forming parallel to an axial-planar and shear-band cleavage, and bedding-parallel shear veinlets with oblique fiber orientations. The post-folding Cu-Co mineralization consists of veins that cross-cut earlier veins and folds.Microthermometric analysis of fluid inclusion assemblages from the pre-, syn-, as well as post-folding veins reveals the presence of different fluid types. A high-temperature (180–340 °C) and high-salinity (27–52.5 wt% NaCl + (KCl) eq.) fluid was responsible for the Cu-Co mineralization during the pre- to syn-folding stages. A hypersaline fluid (27.0–42.1 wt% NaCl eq.) with a broad range in temperature (45–387 °C) circulated during the post-folding stage of the Lufilian orogeny. A fluid exhibiting low to moderate homogenization temperatures (28–215 °C) and low to moderate salinity (3.4–23.0 wt% NaCl eq.) is related to fluid circulation during the post-Lufilian epoch. The wide range and variations in salinity of these three fluid types associated with Cu-Co mineralization provide evidence for a multistage fluid flow and a complex hydrothermal system linked to the deposition of Cu-Co ores within the Tenke Fungurume Mining District and the broader Katanga basin. This hydrothermal system has operated during diagenesis, the basin development stage to the Lufilian orogeny and the subsequent post-Lufilian period.

Genetic mechanism and petroleum geological significance of calcite veins in organic-rich shales of lacustrine basin: A case study of Cretaceous Qingshankou Formation in Songliao Basin, China

Based on the observation and analysis of cores and thin sections, and combined with cathodoluminescence, laser Raman, fluid inclusions, and in-situ LA-ICP-MS U-Pb dating, the genetic mechanism and petroleum geological significance of calcite veins in shales of the Cretaceous Qingshankou Formation in the Songliao Basin were investigated. Macroscopically, the calcite veins are bedding parallel, and show lenticular, S-shaped, cone-in-cone and pinnate structures. Microscopically, they can be divided into syntaxial blocky or columnar calcite veins and antitaxial fibrous calcite veins. The aqueous fluid inclusions in blocky calcite veins have a homogenization temperature of 132.5–145.1 °C, the in-situ U-Pb dating age of blocky calcite veins is (69.9±5.2) Ma, suggesting that the middle maturity period of source rocks and the conventional oil formation period in the Qingshankou Formation are the sedimentary period of Mingshui Formation in Late Cretaceous. The aqueous fluid inclusions in fibrous calcite veins with the homogenization temperature of 141.2–157.4 °C, yields the U-Pb age of (44.7±6.9) Ma, indicating that the middle-high maturity period of source rocks and the Gulong shale oil formation period in the Qingshankou Formation are the sedimentary period of Paleocene Yi'an Formaiton. The syntaxial blocky or columnar calcite veins were formed sensitively to the diagenetic evolution and hydrocarbon generation, mainly in three stages (fracture opening, vein-forming fluid filling, and vein growth). Tectonic extrusion activities and fluid overpressure are induction factors for the formation of fractures, and vein-forming fluid flows mainly as diffusion in a short distance. These veins generally follow a competitive growth mode. The antitaxial fibrous calcite veins were formed under the driving of the force of crystallization in a non-competitive growth environment. It is considered that the calcite veins in organic-rich shale of the Qingshankou Formation in the study area has important implications for local tectonic activities, fluid overpressure, hydrocarbon generation and expulsion, and diagenesis-hydrocarbon accumulation dating of the Songliao Basin.

Understanding the Hydrocarbon Accumulation Process in Deep–ultradeep Oil and Gas Reservoirs in Complex Structural Areas—The Qixia Formation in the Shuangyushi Structure in Northwestern Sichuan Basin, China

Deep-ultradeep oil and gas reservoirs in complex structural areas have typically undergone multistage tectonic processes that have a considerable influence on the hydrocarbon composition, isotopic composition, and other geochemical characteristics of petroleum. By assessing the charging period of hydrocarbon accumulation during a particular age we can determin these changes. We studied the characteristics of fluid inclusions developed in the dolomite reservoir in the Middle Permian Qixia Formation in the Shuangyushi structure of the northwestern Sichuan Basin using methods such as inclusion petrography, microbeam fluorescence fluorescence spectroscopy, and inclusion homogenization temperature. Furthermore, the main peak wavelength of the fluorescence spectrum, red–green ratio/chromatic parameter, Q650/500, as well as the chromatic parameter corresponding to emission flux at 535 nm (QF535) and their correlations with the homogenization temperature distribution, were used to identify the charging period of hydrocarbons in the Qixia Formation. The results show that different types of fluid inclusions were developed in the Qixia Formation. The fluorescence of hydrocarbon inclusions is mainly blue, with a small amount of yellow–green and orange–yellow. The max of orange–yellow, yellow–green, and blue fluorescence of the hydrocarbon inclusions range between 562 ∼ 579 nm, 497 ∼ 548 nm, and 447 ∼ 497 nm, respectively. The distribution of the homogenization temperatures during the same period ranges from 100 °C to 110 °C, from 120 °C to 140 °C, and from 160 °C to 170 °C, respectively. By combining the burial and thermal evolution histories of the Qixia Formation, we concluded that the Qixia Formation has experienced three stages of oil and gas charging, with the time of 204, 185 and 158 Ma. This method is of great significance to determine the date and duration of oil and gas accumulation, and provides technical support for the recovery of ultra-deep hydrocarbon accumulations in complex structural areas.

An efficient two-stage heating strategy for embedded heat pipe system considering power and energy requirements from battery

The battery thermal management system (BTMS) embedded heat pipe system cannot only quickly heat the battery, but also improve its temperature consistency. In order to accurate predict the electro-thermal performance of the battery pack with such a BTMS, an electro-thermal model integrating heat pipe model is established for the pack. This model extends the traditional RC model to a dual-RC model at the cell level for predicting the cell anode potential, which clearly senses the status of lithium plating during the heating process. At the pack level, a distributed electro-thermal model combined with a thermal resistance network-based heat pipe model is proposed for the precise determination of the overall pack temperature. To further enhance the accurate monitoring of lithium plating status and control of the heating process for each cell within the pack, the control criterion is based on the terminal voltage rather than the state of charge (SOC). Additionally, an absolute SOC is defined to unify the SOC calculation across different low-temperature scenarios. With the assistance of the model frameworks above, a two-stage heating strategy is proposed for the BTMS, including the power requirement stage to ensure the heating rate and energy requirement for more available depth of discharge (DoD). In the stage of power requirement, air parameters are determined as Vair = 9 m/s and Tair = 60 °C, and the corresponding temperature rising rates are 1.05 °C/min under discharge and 1.08 °C/min under charge condition, respectively. Additionally, in order to ensure the high heating rate and 98 % available DoD, the second stage heats the pack with the air parameters of Vair = 5 m/s and Tair = 60 °C, with the temperature rising rates of 1.02°C/min under discharge and 1.74°C/min under charge condition. Unlike the air parameters used in the first phase, those in second phase also considers the energy conservation of the BTMS and temperature homogeneity inside the pack. The energy consumptions of BTMS are 0.323 kW·h for the discharging and 0.133 kW·h for the charging. Moreover, the tested temperature difference among cells in the whole heating process is no more than 1.3 °C.