Sulfur Elements Research Articles

Pressure-tolerant survival mechanism of Schizophyllum commune 20R-7-F01 isolated from deep sediments 2 kilometers below the seafloor

In anaerobic high hydrostatic pressure (HHP) sedimentary environments below the seafloor, fungi are found to dominate the eukaryotic communities, playing crucial ecological roles. However, the specific mechanisms by which fungi adapt to anaerobic HHP environments remain unclear. In this study, we investigated Schizophyllum commune 20R-7-F01 isolated from coal-bearing sediments at a depth of 2 km below the seafloor. By assessing the cell viability, biomass, and cell wall thickness changes of strain 20-7-1 under different HHP conditions, we observed that, compared to 0.1 MPa, strain 20-7-1 exhibited slower growth rates and decreased cell viability at 15 MPa and 35 MPa, yet demonstrated significant pressure tolerance. Transcriptomic and metabolomic analyses revealed that this strain activated the carbohydrate metabolic process to simultaneously utilize ethanol and lactic acid fermentation pathway. Additionally, it activates the oxidoreductase activity and hydrolase activity pathways to detoxify intracellular reactive oxygen species (ROS). Activation of the metal ion binding pathway increases the proportion of unsaturated fatty acids in the cell membrane, while instigation of the integral component of membrane pathway maintains cell wall structural stability. Furthermore, activation of the DNA repair pathway repairs DNA damage, demonstrating its comprehensive adaptive mechanisms against the HHP stress. These research findings deepen our understanding of fungal survival strategies and adaptation mechanisms in extreme environments, laying the groundwork for further exploration of their roles in cycling of carbon, nitrogen, sulfur, and other elements in the deep biosphere.

Metallogenic model of sandstone-hosted copper deposits: a case study from the Paleogene in Jiashi area, northwestern China

Sandstone-hosted copper deposits, a type of Sediment-Hosted Stratiform Copper (SSC) deposits, are widely distributed globally. While economically viable deposits of SSC are relatively scarce, they account for approximately 30 % of the world's total discovered copper resources. However, there is still a lack of comprehensive and in-depth research into the depositional and metallogenic models of these deposits. The Jiashi area of the Tarim Basin in northwestern China, known for its economically significant Paleogene SSC deposit, lacks in-depth studies on metallogenic processes. To address this, field profile observations were conducted to analyze the sedimentary evolution, sequence stratigraphy, and tectonism of the Paleogene strata in the Jiashi area. Combined with elemental geochemical analysis of samples, the provenance of sediment, and the source of metallogenic materials, a robust metallogenic model was established. The results reveal the influence of provenance for the origin of Paleogene copper-rich strata. Sedimentary evolution played a crucial role in controlling the distribution of copper and sulfur elements, as well as the spatial arrangement of metallogenic beds. Additionally, nappe movement potentially generated faults, allowing upward movement of basin fluids, which played a crucial role in the formation of copper deposits within sandstone-hosted systems. Thus, this study offers a comprehensive analysis of the metallogenic processes involved in sandstone-hosted copper deposits, thereby contributing significant insights to the broader research on SSC deposits worldwide.

Synergistic promotion mechanism and structure-function relationship of nonmetallic atoms doped carbon nanodots driving Tagetes patula L. to remediate cadmium-contaminated soils

Phytoremediation is an economical and effective strategy to remove cadmium (Cd) from polluted environments. To improve its efficiency, nanotechnology has been proposed to collaborate with hyperaccumulators in the remediation of Cd-polluted soils. However, the intricate structure-function relationship and the underlying regulatory mechanisms by which nanomaterials regulate Cd migration and conversion within the soil-plant system remained unrevealed. In this study, functional carbon nanodots (FCNs) were modified by doping with nitrogen and (or) sulfur elements. The synthesized nonmetallic atoms-doped FCNs were utilized to investigate their structure-function relationship and the regulatory mechanisms underlying their role in the phytoremediation of Cd-polluted soils by Tagetes patula L. FCNs-based nanomaterials can regulate the migration and bioaccumulation of Cd in the soil-plant system, which exhibits an obvious structural dependency. Specifically, the synergistic application of sulfur doped FCNs and Tagetes patula L. had the highest Cd removal efficiency of 53.2%, which was 20.1% higher than Tagetes patula L. alone. The uptake and migration of Cd in the soil-plant system are regulated by FCNs-based nanomaterials through both direct and indirect mechanisms, involving interfacial reactions, plant physiology regulation and environmental influence. This study not only sheds light on the fate of FCNs-based nanomaterials and Cd in the soil-plant system, but also provides innovative nanotools for reinforcing phytoremediation efficiency in contaminated soils.

Transforming Element Sulfur to High Performance Closed‐Loop Recyclable Polymer via Proton Transfer Enabled Anionic Hybrid Copolymerization

AbstractThe utilization of sulfur has been a global issue. Copolymerization of element sulfur (S8) with other monomers is a promising route to convert it to useful materials but is limited by the comonomers. Here, we report anionic hybrid copolymerization of S8 with acrylate and epoxide at room temperature, where S8 does not copolymerize with epoxide in the absence of acrylate. Yet, the proton transfer from the methyne in acrylate to the oxygen anion enables the ring‐opening of the cyclic comonomer and hence the copolymerization. The cyclic comonomers can be expanded to lactone and cyclic carbonate. Specifically, the copolymer of S8 with bisphenl A diglycidyl ether and diacrylate displays mechanical properties comparable to those of most common plastics, namely, it has ultimate tensile strength as high as 60.8 MPa and Young's modulus up to 680 MPa. It also exhibits high UV resistance and good transparency. Particularly, it has excellent UV‐induced self‐healing, reprocessability and closed‐loop recyclability due to the abundant dynamic S−S bonds and ester groups. This study provides an efficient strategy to turn element sulfur into closed‐loop recyclable polymer with high mechanical and optical performances.

Green fabrication of cost-effective and sustainable nanoporous carbons for efficient hydrogen storage and CO2/H2 separation

In this study, sustainable nanoporous carbon materials that are efficient, renewable, cost-effective and adaptable were developed. These microporous feature carbon adsorbents were synthesized utilizing a straightforward and efficient method. Plum stones are residual fruit materials that offer a financially feasible and sustainable carbon source with exceptional porosity and desirable elemental composition. The plum stones underwent carbonization and were subsequently chemically modified with polyaniline nanofibers and then subjected to chemical activation using different activating agents. This yielded sustainable nanoporous carbon with a high degree of porosity, in conjunction with doping with precious high electron density elements such as O, N and S. The sustainable nanoporous carbons that have been developed exhibits exceptional microporosity, with BET-SSA of 1705 m2 g−1 and a pore volume of 0.726 cm3 g−1, besides, the dominance of ultramicropores of 0.6 nm size. This in addition to convenient doping of oxygen, nitrogen and sulfur elements which are crucial for H2 uptake. The developed nanoporous carbon demonstrated highly promising capabilities for storing H2 molecules at cryogenic and ambient temperatures. The sustainable adsorbent achieved hydrogen storage capacities of 4.63 and 0.45 wt% at 77, 296 K, and a pressure of 40 and 80 bar, respectively. This H2 storage capacity at RT is often regarded as one of the highest reported in the literature for nanoporous adsorbents. Moreover, study investigated the separation selectivity of developed adsorbents for CO2/H2 based on uptake ratio at 30 bar and RT. The results demonstrated a significant separation selectivity reaching a value of 382.5 for the CO2/H2, which is regarded as one of the most elevated values documented in the existing literature for nanoporous carbon materials. Thus, the presented sustainable nanoporous materials have shown great promise for hydrogen storage, pre-combustion CO2 capture and H2 purification applications at ambient temperature.

The Application of Sulfur–Metal Mass Ratios in Metal Sulfides in Assessing Prospects for Deep Metallogeny: A Case Study of the Tongshan Copper Deposit in Heilongjiang Province, Northeast China

Sulfur–metal mass ratios (SMMRs) between sulfur and metal elements (Cu, Pb, Zn, Ag, Fe, etc.) in metal sulfides are fixed in idealized compositions, so they should have a relatively fixed proportion in terms of mass without considering the presence of structural defects such as vacancies or substitution elements. Rock bodies with an SMMR of S far greater than the common metal sulfides may contain additional sulfides of other metals. We studied the Tongshan copper deposit in NE China and calculated the mass transfer of various elements in drill hole ZK611 samples. The data show a S influx of 7160 g/t, a Cu influx of 5469 g/t, and an Fe influx of 8796 g/t in the Cu ore body. Below the Cu ores, the average influx is 18,600 g/t of S, 650 g/t of Cu, and 5360 g/t of Fe, which provides an SMMR far above common mineral sulfide values. Further studies indicated that this rock unit contains fine-grained sphalerite and galenite, and when Zn and Pb are included in the rock SMMR calculations, values closer to the mineral sulfides emerge. These results imply that the coordinating balance relationship of S content with Fe and other ore-forming metals could provide direct information for assessing metallogenic prospects.

Impact of Sulfur Deficiency and Excess on the Growth and Development of Soybean Seedlings.

Sulfur is a critical element for plant growth and development, serving as a component of amino acids (cysteine and methionine), iron-sulfur clusters, proteins, glutathione, coenzymes, and auxin precursors. Deficiency or low concentrations of sulfur in the soil can lead to significant growth retardation in plants. The objective of our study was to examine the effects of sulfur (S) deficiency and excess on morphological symptoms, sulfur and nitrogen (N) metabolism, as well as antioxidant activity in soybean. We found that S starvation decreased the fine root length, biomass, and activity, and the chlorophyll content was reduced, while excess sulfur promotes lateral root growth. In contrast to sulfur excess, sulfur deficiency inhibits N and S metabolism levels in both subsurface and above-ground parts, and induced the expression of some sulfur transporters (SULTRs). In this study, we created soybean hairy root lines overexpressing the SULTR gene (GmSULTR2;1a) to observe metabolic changes following sulfur deficiency treatment. The results showed that GmSULTR2;1a saved the sulfur-deficient phenotype, and the antioxidant enzyme activity was much higher than that of the wildtype in the absence of sulfur. Our study revealed the important role of sulfur element in soybean growth and development and the regulation of sulfur deficiency by GmSULTR2;1a.

Effects of Anchovy, Mussel, and Shrimp Powders on the Flame Retardancy of Bacterial Cellulose

ABSTRACT This study aims to fabricate bacterial cellulose with improved flame retardancy by applying anchovy, mussel, and shrimp powders. The elemental analysis confirmed that raw marine powders contained nitrogen and sulfur elements which could play important roles in enhancing the flame retardancy of bacterial cellulose. Thermogravimetric analysis revealed the improved thermal stability of bacterial cellulose following entrapping and crosslinking of the marine powders. The fabricated bacterial celluloses with marine powders had similar levels of flame retardancy as that of bacterial cellulose treated with a commercial flame-retardant, sodium metasilicate nonahydrate, which was confirmed by the vertical flammability test and limiting oxygen index. The char morphology analysis revealed intumescent char on the surface of the samples, confirming the effect of marine powders on the flame retardancy of bacterial cellulose. Moreover, the marine powders were entrapped and crosslinked with bacterial cellulose nanostructures, and the chemical and crystalline structures of bacterial cellulose were retained. This study proposes an efficient method to improve the flame retardancy of bacterial cellulose by introducing marine powders via the combined entrapment and crosslinking method.

3D Tunnel Copper Tetrathiovanadate Nanocube Cathode Achieving Ultrafast Magnesium Storage Reactions through a Charge Delocalization and Displacement Mechanism.

Rechargeable magnesium batteries are attractive candidates for large-scale energy storage applications because of the low cost and high safety, but the scarcity and inferior performance of the cathode materials are hindering the development. In the present study, a kind of copper tetrathiovanadate (Cu3VS4) cathode is designed and developed with a comprehensive consideration of the chemical and electronic structures. The vanadium and sulfur atoms form chemical bonds with high covalent proportion, facilitating electron delocalization via the vanadium-sulfur bonds. This reduces the interaction with the bivalent magnesium cation and induces the coredox of vanadium and sulfur. The crystal structure of Cu3VS4 has interlaced 3D tunnels for solid-state magnesium cation transport. The Cu3VS4 cathode shows a high capacity of 350 mA h g-1 at 100 mA g-1, an outstanding rate performance of 67 mA h g-1 at 10 A g-1, and stable cycling for 1000 cycles at 5 A g-1 without obvious capacity fading. Prominently, a high areal mass load of 3.5 mg cm-2 could be achieved without obvious rate capability decay, which is quite favorable to pair with the high-capacity magnesium metal anode in practical application. The mechanism investigation and theoretical computation demonstrate that Cu3VS4 undergoes first a magnesium intercalation and then a displacement reaction, during which the crystal structure is maintained, assisting the reaction reversibility and cycling stability. All the copper, vanadium, and sulfur elements experience redox and contribute to the high capacity. Moreover, the weakened interaction with magnesium cations, well-kept 3D cation transport tunnels, and high electronic conductivity result in the superior rate performance and high areal active material loading. The present study develops a high-performance cathode for rechargeable magnesium batteries and reveal the design principle based on both of chemical and electronic structures.

Cyclosulfate additive inhibits Li dendrite disorder growth to achieve stable cycles of Li metal battery

ABSTRACT The high reactivity of lithium metal leads to the uncontrolled growth of lithium dendrites during the charging and discharging process of lithium metal batteries, which results in the poor cycle performance of batteries. In this paper, we innovatively utilized 1, 3-propanediol cyclic sulfate (PCS) as an additive to successfully construct a smooth and dense SEI layer containing sulfur element on the lithium metal anode surface. Under the action of PCS, the cells show excellent performance. After 200 cycles, cells with baseline electrolyte (BE) + 1 wt.% PCS still has a high capacity of of 148mAh g−1 and 81.38% capacity retention compared with cells with BE. In-situ optical microscopy is pioneeringly applied to showcase the generation and growth of lithium dendrites which showed that PCS participated in the formation of the SEI layer, indicating that this optimized SEI layer has better conductivity of Li+ and chemical stability, thus inhibiting malignant lithium deposition and electrolyte decomposition above the lithium metal anode.

Efficient Synthesis of Dithieno[3,2‐B:2’,3’‐d]Thiophenes Derivatives with Promising Optoelectronic Properties Via a One‐Pot, Two‐Step Method with Elemental Sulfur

AbstractDithieno[3,2‐b:2’,3’‐d]thiophene (DTT) derivative contains three annulated thiophene rings, which have attracted great attention in the field of materials due to its planar and conjugated molecular, structural rigidity, and increased solubility. Herein, the one‐step modular construction of a series of structurally well‐defined 2,6‐disubstituted dithieno[3,2‐b:2’,3’‐d]thiophenes (2,6‐DTT) involves Pd/Cu(I)‐catalyzed Sonogashira coupling and LiNH2‐mediated ring‐closing reaction with element sulfur was reported. The method allows the selective and straightforward introduction of different aryl substitution into DTT without otherwise tedious separation and purification processes. The preliminary study of the thermal and photophysical properties demonstrated that the introduction of substituent in phenyl has great impact for the parent molecule, which enable this protocol to synthesis high‐performance 2,6‐DTT through the different alkynes.

Sulfur modified N-doped carbocatalysts promote the selectivity for H2S selective oxidation

Sulfur element is widely applied as a non-metallic dopant into carbon framework for the modulation of their chemical activities. An interesting question is whether the intrinsic catalytic performances for the H2S selective oxidation to sulfur can be manipulated by sulfur element introduction into carbocatalysts. In this study, we employ a simple solvent-free method to introduce S atoms into framework of N-doped carbocatalysts, resulting in a notable enhancement of the product S selectivity with negligible loss of H2S selective oxidation. The experimental results show that the as-synthesized N-S-C-2 catalyst exhibits a H2S conversion of 97.5 % and sulfur selectivity of >80 % at a high O2-to-H2S ratio (2.5) under continuous mode (over the dew point temperature of sulfur, c.a. 210 °C), while also demonstrating robust stability (> 100 h), anti-CO2 (up to 50 vol%) and anti-oxidation properties. Kinetic analysis and H2S/O2-TPD-MS results reveal that S introduction attenuates the adsorption and dissociation of H2S and O2 by the N-doped carbon catalyst. Furthermore, density functional theory calculations elucidate that S doping elevates the adsorption energies of H2S and O2 at the pyridinic N site, thereby moderately reducing the adsorption of H2S and O2, consequently preventing the over-oxidation of H2S to SO2 and enhancing S selectivity. The double doping promotion effect of carbon materials reported in this investigation offers an alternative insight for the development of highly selective carbon desulfurization catalysts.

Acidophilic sulphate-reducing bacteria: Diversity, ecophysiology, and applications.

Acidophilic sulphate-reducing bacteria (aSRB) are widespread anaerobic microorganisms that perform dissimilatory sulphate reduction and have key adaptations to tolerate acidic environments (pH <5.0), such as proton impermeability and Donnan potential. This diverse prokaryotic group is of interest from physiological, ecological, and applicational viewpoints. In this review, we summarize the interactions between aSRB and other microbial guilds, such as syntrophy, and their roles in the biogeochemical cycling of sulphur, iron, carbon, and other elements. We discuss the biotechnological applications of aSRB in treating acid mine drainage (AMD, pH <3), focusing on their ability to produce biogenic sulphide and precipitate metals, particularly in the context of utilizing microbial consortia instead of pure isolates. Metal sulphide nanoparticles recovered after AMD treatment have multiple potential technological uses, including in electronics and biomedicine, contributing to a cost-effective circular economy. The products of aSRB metabolisms, such as biominerals and isotopes, could also serve as biosignatures to understand ancient and extant microbial life in the universe. Overall, aSRB are active components of the sulphur and carbon cycles under acidic conditions, with potential natural and technological implications for the world around us.

Improving the Performance of LiFePO4 Cathodes with a Sulfur-Modified Carbon Layer

LiFePO₄ (LFP) cathodes are popular due to their safety and cyclic performance, despite limitations in lithium-ion diffusion and conductivity. These can be improved with carbon coating, but further advancements are possible despite commercial success. In this study, we modified the carbon coating layer using sulfur to enhance the electronic conductivity and stabilize the carbon surface layer via two methods: 1-step and 2-step processes. In the 1-step process, sulfur powder was mixed with cellulose followed by heat treatment to form a coating layer; in the 2-step process, an additional coating layer was applied on top of the carbon coating layer. Electrochemical measurements demonstrated that the 1-step sulfur-modified LFP significantly improved the discharge capacity (~152 mAh·g−1 at 0.5 C rate) and rate capability compared to pristine LFP. Raman analyses indicated that sulfur mixed with a carbon source increases the graphitization of the carbon layer. Although the 2-step sulfur modification did not exceed the 1-step process in enhancing rate capability, it improved the storage characteristics of LFP at high temperatures. The residual sulfur elements apparently protected the surface. These findings confirm that sulfur modification of the carbon layer is effective for improving LFP cathode properties, offering a promising approach to enhance the performance and stability of LFP-based lithium-ion batteries.

Unveiling the competitive mechanism between SO2 and PCDD/Fs on activated carbon adsorption

In municipal solid waste incineration (MSWI) plants, activated carbon (AC) adsorption is the key technique for eliminating Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from flue gases. This research thoroughly investigates the potential competitive adsorption between SO2 and PCDD/Fs and examines how adsorption at the center and the edge of the AC layer impacts the adsorption process. The findings show a decline in the removal efficiency of PCDD/Fs from 86.8 % to 84.2 % and further to 74.4 % when using SO2 pre-treated (AC-A3) and H2SO4-impregnated (AC-B2) activated carbon, respectively. Multiple characterization methods reveal that sulfur elements occupy active sites within the inner pores of the activated carbon, reducing the availability of its pore structure, particularly affecting microporous more than mesoporous structures. DFT calculations suggest that the π-π EDA effect facilitates the adsorption of 2,3,7,8-Tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD), whereas dispersion force drive SO2 adsorption. Comparisons among various oxygenated functional groups show that the organic acid anhydride (CO-CO) has better adsorption selectivity toward TCDD and less adsorption to SO2. This study provides a novel perspective on the adsorption mechanisms of PCDD/Fs on AC and the competitive dynamics of sulfur in the flue gas.

Nutrient removal performance and the nitrogen-sulfur conversion pathways in sulfur-iron based biofilter under acidic/alkaline conditions

The nitrate and phosphate removal in sulfur based (Vp) and sulfur-iron based autotrophic denitrification systems (Sp) with sponge iron as the iron source was investigated under different pH (6–9). In this study, Sp (>98 %) and Vp (>97 %) had higher nitrate removal efficiency at pH 7–8 and the highest phosphate removal efficiency (94.9 % ± 3.57 %) at pH 6. The flow cytometry detection revealed that the cell integrity was damaged due to the formation of iron crusts at pH 6, which resulted in irreversible inhibition in Sp. Electron transfer and nitrogen transformation showed that compared with the sustained inhibition of denitrification at pH 6, the inhibition at pH 9 occurred mainly in the initial 0–2 h due to the enhanced flow of electrons toward the formation of biological element sulfur (Sbio0). Coupled sponge iron promoted the adsorption and reduction of NO2−/N2O and reduced N2O emissions. Metatranscriptomics analysis showed that significant upregulation of key gene expression for nitrogen and sulfur metabolism in Sp, with complex regulatory mechanisms enhancing system stability and performance. Acidic conditions reduced the abundance of denitrification and sulfur oxidation functional genes. However, alkaline conditions (pH of 9) mainly caused the decreased abundance of denitrification functional genes, which was favorable for accumulation of Sbio0. This study provides a theoretical basis for the stable operation and regulation of the sulfur-iron based autotrophic denitrification process.

A novel magnetic S/N co-doped tea residue biochar applied to tetracycline adsorption in water environment

The issue of tetracycline (TC) contamination has attracted widespread attention. Adsorption technology has great potential for application in the field of TC remediation. This study achieved the production of nitrogen self-doped biochar using waste tea leaves as raw materials, and further improved its TC removal effect by doping sulfur elements. A recyclable high-performance TC adsorbent magnetic S/N co-doped tea residue biochar (MSNB) was obtained through ferromagnetic modification, which could be used as an effective TC adsorbent. The effects of MSNB dosage and initial solution pH on TC removal were evaluated. The recovery performance of MSNB adsorbent on TC was studied. The maximum adsorption performance at 298 K calculated using the Langmuir model was 140.76 mg g−1. The fitting results of adsorption kinetics indicated that chemical adsorption was the main factor affecting the adsorption reaction. After 5 cycles of adsorption, the removal of TC by MSNB remained above 88.30 %. This study could provide theoretical support for the treatment of tetracycline wastewater by biochar adsorption.

Mechanistic insights into Fe3O4-mediated inhibition of H2S gas production in sludge anaerobic digestion

The addition of iron-based conductive materials has been extensively validated as a highly effective approach to augment methane generation from anaerobic digestion (AD) process. In this work, it was additionally discovered that Fe3O4 notably suppressed the production of hazardous H2S gas during sludge AD. As the addition of Fe3O4 increased from 0 to 20 g/L, the accumulative H2S yields decreased by 89.2 % while the content of element sulfur and acid volatile sulfide (AVS) respectively increased by 55.0 % and 30.4 %. Mechanism analyses showed that the added Fe3O4 facilitated sludge conductive capacity, and boosted the efficiency of extracellular electron transfer, which accelerated the bioprocess of sulfide oxidation. Although Fe3O4 can chemically oxidize sulfide to elemental sulfur, microbial oxidation plays a major role in reducing H2S accumulation. Moreover, the released iron ions reacted with soluble sulfide, which promoted the chemical equilibrium of sulfide species from H2S to metal sulfide. Microbial analysis showed that some SRBs (i.e., Desulfomicrobium and Defluviicoccus) and SOB (i.e., Sulfuritalea) changed into keystone taxa (i.e., connectors and module hubs) in the reactor with Fe3O4 addition, showing that the functions of sulfate reduction and sulfur oxidation may play important roles in Fe3O4-present system. Fe3O4 presence also increased the content of functional genes encoding sulfide quinone reductase and flavocytochrome c sulfidedehydrogenase (e.g., Sqr and Fcc) that could oxidize sulfide to sulfur. The impact of other iron-based conductive material (i.e., zero-valent iron) was also verified, and the results showed that it could also significantly reduce H2S production. These findings provide new insights into the effect of iron-based conductive materials on anaerobic process, especially sulfur conversion.

Genesis of Yongping copper deposit in the Qin-Hang Metallogenic Belt, SE China: Insights from sulfide geochemistry and sulfur isotopic data

Yongping copper deposit is a large-scale polymetallic mine that contains 1.6 Mt of proven Cu metal reserves with an average grade of 0.74 % and contributes significantly to China’s production of copper. This deposit is situated in the eastern part of the Qin-Hang Metallogenic Belt (Jiangxi province, SE China) at the contact zone between the Yangtze Cu–Mo metallogenic belt and the Jiangxi W–Sn–REE metallogenic belt. The thick stratiform and lenticular-shaped orebodies are hosted in the Carboniferous Yejiawan Formation, consisting of sandstone, limestone, mudstone, and chert-rich clastic rocks. Dominant metal-bearing minerals are chalcopyrite and pyrite with a minor amount of sphalerite, tetrahedrite, galena, molybdenite, pyrrhotite, magnetite, hematite, and scheelite. Although intensive research has been done on its geological setting, geochemical characteristics, and geodynamic evolution over the past thirty years, the origin and depositional environments have remained controversial. In the current research, in situ trace element geochemistry and sulfur isotope analyses, coupled with microscopic investigation, were conducted on sulfide minerals using the LA-ICP-MS technique. The results display that Yongping pyrite rich in Co, As, Ni, Zn, Cu, and Te and deplete in other trace elements. Sphalerite rich in Fe, Mn, Cu, and Cd, followed by In, Co and Ga. The calculation results of formula T(°C) = (Fe/Zn + 0.2953)/(0.0013) reveal that sphalerite was formed in medium–high temperature conditions (262 °C–377 °C). The δ34SV-CDT values of studied sulfides (pyrite, chalcopyrite, sphalerite, and tetrahedrite) varied from −1.52 ‰ to 5.13 ‰ with an average of 2.36 ‰, which are highly consistent with those recorded from porphyritic biotite granite stock of Shizitou (from 2.20 ‰ to 4.5 ‰), suggesting a dominantly magmatic origin. Collectively, trace element compositions of analyzed sphalerite and pyrite from the Yongping area exhibit characteristics of typical skarn deposits. Combined with previous studies, we can conclude that the Yongping Cu deposit is a skarn deposit that was most likely formed by contact metasomatism after the intrusion of the Jurassic Huoshaogang-Shizitou granitic stock into the Carboniferous Yejiawan Formation.

Transforming Element Sulfur to High Performance Closed-Loop Recyclable Polymer via Proton Transfer Enabled Anionic Hybrid Copolymerization.

The utilization of sulfur has been a global issue. Copolymerization of element sulfur (S8) with other monomers is a promising route to convert it to useful materials but is limited by the comonomers. Here, we report anionic hybrid copolymerization of S8 with acrylate and epoxide at room temperature, where S8 does not copolymerize with epoxide in the absence of acrylate. Yet, the proton transfer from the methyne in acrylate to the oxygen anion enables the ring-opening of the cyclic comonomer and hence the copolymerization. The cyclic comonomers can be expanded to lactone and cyclic carbonate. Specifically, the copolymer of S8 with bisphenl A diglycidyl ether and diacrylate displays mechanical properties comparable to those of most common plastics, namely, it has ultimate tensile strength as high as 60.8 MPa and Young's modulus up to 680 MPa. It also exhibits high UV resistance and good transparency. Particularly, it has excellent UV-induced self-healing, reprocessability and closed-loop recyclability due to the abundant dynamic S-S bonds and ester groups. This study provides an efficient strategy to turn element sulfur into closed-loop recyclable polymer with high mechanical and optical performances.