Metal Resources Research Articles

A Planetary Boundary for Mineral, Metal, and Fossil Resource Extraction Rates: How Much Primary Materials Can a Circular Economy Extract?

Resource consumption is expected to further increase in the next decades. A circular economy could decrease the environmental impact of this resource consumption by minimizing the primary raw materials consumption and minimizing emissions that render materials inaccessible for further use. However, such a circular economy will still have primary raw material inflows, due to population growth, stock expansion, energy transition, and inevitable dissipation. The potential magnitude of such primary raw material inflows in a circular economy remains unclear. To address this uncertainty, the planetary boundary framework, which defines absolute limits on resource and emission flows, could be utilized. Although this framework incorporates aspects of biomass, water, and land use, mineral, metal, and fossil resources are not included. This study provides a principle for a planetary boundary for these three resources, based on the net accessibility rate and an allocated share of the accessible resource stock in the ecosphere. Inter- and intragenerational equality are crucial for determining this allocated share and for quantifying a sustainable rate of resource extraction in (an economy transitioning toward) a circular economy. Next steps to operationalize this principle provide further guidance to determine the safe operating space for mineral, metal, and fossil resource extraction.

Sustainable extraction and recycling of non-ferrous metals: a review from a European perspective.

This review article provides a comprehensive examination of sustainable extraction and recycling methods for non-ferrous metals, which are critical to a wide range of industries including electronics, construction and renewable energy. Focusing on metals such as aluminium, copper and silicon, the study highlights the importance of recycling in conserving resources and minimizing environmental impact. It discusses the challenges posed by material diversity in recycling processes and the advances in recycling technologies that have emerged in response. Special emphasis is placed on the importance of a circular economy in maintaining a sustainable balance between consumption and conservation of metal resources. Through detailed analysis, it advocates innovative recycling practices and improved design for recyclability and highlights the role of policy, industry and consumer behaviour in achieving sustainability goals. The findings contribute to the discourse on strategic self-sufficiency in Europe through recycling, providing insights into how to improve efficiency and manage the complexity of the global material cycle. This work calls for a collaborative effort towards sustainable metallurgy and underlines the critical need for advances in recycling infrastructure and technology to ensure the long-term availability and environmental stewardship of non-ferrous metals.This article is part of the discussion meeting issue 'Sustainable metals: science and systems'.

Self-catalytic enhancement of Cu-EDTA decomplexation and simultaneous Cu recovery via a dual-cathode electrochemical process

Heavy metals that are readily chelated with coexisting organic ligands in industrial wastewaters impose threats to environment and human health but are also valuable metal resources. Traditional treatment methods generally require additional chemicals and generate secondary contaminants. Here, a reagent-free dual-cathode electrochemical system was proposed for the efficient destruction of Cu-organic complexes and synchronous cathodic recovery of Cu, whereby in situ production of H2O2 at carbon aerogel (CA) cathode was coupled with the reduction of Cu(II) to Cu(I) and finally to Cu(0) at Ti cathode. The intermediate Cu(II) complexes enabled the self-reinforced degradation owing to their higher activities toward •OH generation by activating H2O2 in contrast to initial Cu-ethylenediaminetetraacetic acid (Cu-EDTA). The enhanced production of Cu(I) by Ti cathode facilitated both •OH and Cu(III) formation, and the copper redox cycle was realized in the self-reinforced system, maintaining its sustainable catalytic activity. The energy cost of the dual-cathode system is 0.011 kWh/g for decomplexation and 0.057 kWh/g for Cu recovery, which is much lower than single Ti or CA cathode system. This established process provides a prospective approach for cost-effective destruction of chelating metal complexes and metal resources recovery from heavy metal wastewaters.

Full radionuclide analysis of polymetallic nodules from the Clarion-Clipperton-Fracture Zone in the NE Pacific

Polymetallic Nodules from the deep sea are currently being targeted for mineral exploration as they are a significant resource for various critical metals. In addition to accumulating such metals, nodules are also known to adsorb naturally occurring radioactive nuclides. With the possibility of exploitation of nodules becoming more likely within the next years, it is important to assess the potential radiation exposures resulting from the handling of polymetallic nodules. In this study we present, for the first time, specific activities of all long-lived alpha, beta and gamma emitters from the natural decay chains of Uranium-238, Uranium-235 and Thorium-232, in bulk and surface material of the same nodules obtained from 10 locations within the Clarion-Clipperton Zone. The results show elevated specific activities for the nuclides Th-230, Ra-226, Pb-210, Po-210, as well as Pa-231 and Ac-227 in accordance with prior reported activities. However, in contrast to assumptions made in previous studies, our analyses show that Pa-231 is not in equilibrium with its daughter nuclide Ac-227. The emanation factor of Rn-222 for dry and water-saturated nodules has also been determined and is higher than previously reported. The results presented here are a key ingredient to assess human radiation exposure during the processes of polymetallic nodule mining, storage and beneficiation.

A Typology and Lead Isotope and Cultural Exchange Study on Bronze Knives from Shuangyuan Cemetery, Chengdu City, Southwest China

Background: Bronze knives, which have been excavated in large quantities and acquired hierarchical significance, are essential artifacts in Shu State in Southwest China. Building upon previous typological analyses of bronze knives, it is hypothesized that Shu culture may have imported foreign-style bronze knives. However, further demonstration of the provenance of metal materials, the typology of knives, and the cultural exchange necessitates a comprehensive examination through the lens of scientific analysis. The purpose of this study is to investigate the differences in the manufacturing processes and metal resources of Shu bronze knives with various cultural styles and whether bronze knives in the foreign styles were imported or locally imitated. Methods: In this study, the typology, portable X-ray fluorescence spectrometry and multi-collector inductively coupled plasma mass spectrometry were used to analyze twenty-four bronze knives unearthed from Shuangyuan cemetery, a cemetery of the Eastern Zhou Dynasty in Chengdu City, Sichuan Province, Southwest China. Results: The results of the study show that the knives of Shuangyuan Cemetery can be classified typologically into five types, encompassing both local and foreign styles. The predominant alloy composition of these knives is lead-tin bronze, characterized by a notably high tin content. Lead isotope ratios indicate that metal materials from the South China geochemical province and Yangtze geochemical province were mainly used to manufacture the bronze knives unearthed from the Shu state Conclusion: While the majority of foreign-style knives with ring-shaped heads were likely imported from neighboring regions like Chu state, distinctively styled type D and type E bronze knives appear to have been locally imitated by the Shu, showcasing a blend of external influences and indigenous innovation. The combination of typology and scientific analysis of the bronze knife may shed new light on the study of the Shu culture of the Eastern Zhou period.

Zero-Shot Discovery of High-Performance, Low-Cost Organic Battery Materials Using Machine Learning.

Organic electrode materials (OEMs), composed of abundant elements such as carbon, nitrogen, and oxygen, offer sustainable alternatives to conventional electrode materials that depend on finite metal resources. The vast structural diversity of organic compounds provides a virtually unlimited design space; however, exploring this space through Edisonian trial-and-error approaches is costly and time-consuming. In this work, we develop a new framework, SPARKLE, that combines computational chemistry, molecular generation, and machine learning to achieve zero-shot predictions of OEMs that simultaneously balance reward (specific energy), risk (solubility), and cost (synthesizability). We demonstrate that SPARKLE significantly outperforms alternative black-box machine learning algorithms on interpolation and extrapolation tasks. By deploying SPARKLE over a design space of more than 670,000 organic compounds, we identified ≈5000 novel OEM candidates. Twenty-seven of them were synthesized and fabricated into coin-cell batteries for experimental testing. Among SPARKLE-discovered OEMs, 62.9% exceeded benchmark performance metrics, representing a 3-fold improvement over OEMs selected by human intuition alone (20.8% based on six years of prior lab experience). The top-performing OEMs among the 27 candidates exhibit specific energy and cycling stability that surpass the state-of-the-art while being synthesizable at a fraction of the cost.

Thiourea-linked covalent triazine frameworks enable efficient and selective gold recovery from e-waste leachate

The surging electronic waste (e-waste) has been stimulating the unremitting exploration about the advanced gold recycling technology, which is of great significance to alleviate the shortage of metal resources and minimize the negative environmental impact. Herein, the thiourea-linked covalent triazine frameworks (denoted as PbTu-CTFs) have been designed and constructed by the nucleophilic substitution between cyanuric chloride (CC) and 1,4-phenylene bis(thiourea) (named PbTu) for gold recovery from the actual e-waste leachate. Benefiting from the unique structural characteristics, including large surface areas, abundant porosity, excellent chemical stability, and high-density S, N coordinative sites, the fabricated PbTu-CTFs afford ultrahigh gold adsorption capacity up to 2255 mg/g and fast kinetics, as reflected by 99 % of Au recovery efficiency within 5 min. Meanwhile, satisfactory recyclability and regeneration are maintained after six rounds of consecutive adsorption/desorption tests. Furthermore, the resulting adsorbent is well competent for highly efficient and selective gold recovery from the acidic leaching solution of wasted central processing unit (CPU), exemplify its promising actual application potential.

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.

Efficient leaching of valuable metals from spent lithium-ion batteries using green deep eutectic solvents: Process optimization, mechanistic analysis, and environmental impact assessment

The accumulation of over 11 million tons of spent lithium-ion batteries (LIBs) by 2030 highlights a critical environmental challenge posed by their large-scale retirement. The efficient recycling valuable metals from spent LIBs can both reduces environmental impact and mitigates the pressing issue of metal resource scarcity. In this context, deep eutectic solvents (DESs) have become a promising option as an eco-friendly solvent, exhibiting great potential for recycling spent LIBs. Therefore, this work proposed an innovative green DES system consisting of choline chloride (ChCl), DL-malic acid (MAL), and glycerol for the efficient leaching of valuable metals from spent LIBs. Comprehensive experiments were conducted to determine the optimum leaching conditions (130 °C, 60 g/L, MChCl:MAL:Glycerol of 1:1:3, 3 h), achieving high leaching efficiencies of 94.6% for Ni, 96.8% for Co, 93.8% for Mn, and 96.4% for Li. Through characterization techniques, kinetics studies, and density functional theory (DFT) calculations, the leaching process was predominantly governed by surface chemical reaction (1-(1-x)1/3 = kt) within the shrinking core model, exhibited activation energies of 49.89 kJ/mol, 47.66 kJ/mol, 50.51 kJ/mol, and 22.24 kJ/mol for Ni, Co, Mn, and Li, respectively. The propensity for DES to leach metal ions followed the order: Li > Co > Ni > Mn, determined by binding energy and energy gaps. Cl− and −COOH within the DES were capable of forming stable complexes with reduced transition metal ions, revealing an efficient coordination leaching mechanism. Additionally, a life cycle assessment (LCA) was conducted on the environmental impacts of the DES leaching process, confirming it as an effective and environmentally friendly method for recycling spent LIBs. This work avoided the employment of corrosive acids and alleviated the generally harsh conditions associated with DESs leaching, providing a viable solution for recovering spent LIBs.

The rise and transformation of Bronze Age pastoralists in the Caucasus.

The Caucasus and surrounding areas, with their rich metal resources, became a crucible of the Bronze Age1 and the birthplace of the earliest steppe pastoralist societies2. Yet, despite this region having a large influence on the subsequent development of Europe and Asia, questions remain regarding its hunter-gatherer past and its formation of expansionist mobile steppe societies3-5. Here we present new genome-wide data for 131 individuals from 38 archaeological sites spanning 6,000 years. We find a strong genetic differentiation between populations north and south of the Caucasus mountains during the Mesolithic, with Eastern hunter-gatherer ancestry4,6 in the north, and a distinct Caucasus hunter-gatherer ancestry7 with increasing East Anatolian farmer admixture in the south. During the subsequent Eneolithic period, we observe the formation of the characteristic West Eurasian steppe ancestry and heightened interaction between the mountain and steppe regions, facilitated by technological developments of the Maykop cultural complex8. By contrast, the peak of pastoralist activities and territorial expansions during the Early and Middle Bronze Age is characterized by long-term genetic stability. The Late Bronze Age marks another period of gene flow from multiple distinct sources that coincides with a decline of steppe cultures, followed by a transformation and absorption of the steppe ancestry into highland populations.

Classification and progress of extraction technologies for nonferrous metal resources

Classification and progress of extraction technologies for nonferrous metal resources

High-performance bacterium-enhanced dual-compartment microbial fuel cells for simultaneous treatment of food waste oil and copper-containing wastewater

Microbial fuel cells (MFCs) use the metabolic actions of microorganisms in an anode chamber to convert the chemical energy from wastewater into electrical energy. To improve the MFC power generation performance and chemical oxygen demand (COD) removal efficiency, Stenotrophomonas acidaminiphila was added to the anode chamber of a dual-compartment MFC. In this process, Stenotrophomonas acidaminiphila promotes the degradation of macromolecules such as bis(2-ethylhexyl) phthalate in food waste oil. Additionally, the generated electrical energy reduced Cu2+ in the copper-containing wastewater in the cathode chamber to Cu monomers. The maximum power density of the MFC was 49.5 ± 3.5 mW/m2, the maximum removal efficiencies of COD and Cu2+ were 63.5 ± 5.8% and 96.5 ± 1.0%, respectively, and Cu2+ was reduced to brick-red Cu monomers. This study provides insights into the simultaneous implementation of food waste oil treatment and metal resource recovery.

Sulfide trace element enrichments in the metamorphic basement-hosted Xinhua Pb-Zn-Cu vein-type deposit, eastern Guizhou province (SW China)

Cambrian carbonate formations are widespread in the western Hunan-eastern Guizhou (WHEG) region (southwestern China), which hosts many Mississippi Valley-Type (MVT) lead–zinc (Pb-Zn) deposits. Regional Pb-Zn mineralization is well developed in the low-grade metamorphic rocks of the basal Proterozoic Banxi Group. The mineralization is associated with quartz veins and generally distributed along NE-trending fault zones. Moreover, these deposits have an extensive distribution and high grade, and are associated with Cu-Ag endowment. However, geological and geochemical research on these Pb-Zn vein-type deposits is relatively limited, and their relationship with the regional MVT mineralization remains unclear. The representative Xinhua deposit in Danzhai district is selected as the study subject. We conducted in situ trace element analyses on the sphalerite and chalcopyrite from the various metallogenic stages, and compared them with published sphalerite trace element data from the MVT Pb-Zn deposits in the western Hunan-eastern Guizhou metallogenic belt. Seven orebodies in Xinhua Pb-Zn deposit have been discovered so far, with a metal resource of over 120,000 metric tonnes of Zn + Pb. Field geology and microscopic petrography have revealed two mineralization stages: An early-stage black sphalerite (Sp-I) followed by reddish-brown sphalerite (Sp-II) mineralization, which corresponds to the main chalcopyrite mineralization stage, and a later-stage light-yellow sphalerite (Sp-III), Cu ore-barren mineralization.LA-ICPMS data indicate that the sphalerite from Xinhua has similar trace element compositions to those from the MVT Pb-Zn deposits in the region. They are relatively enriched in Ga, Cd, and Ge, while depleted in Fe, Co, and Mn. Critical metal Ge and Ga are particularly enriched in sphalerite, especially in Sp-I (Ge max 937 ppm, Ga max 824 ppm). The substitution mechanism of Ge and Ga in sphalerite are likely 2Cu+ + Ge4+ ↔ 3Zn2+ and Cu+ + Ga3+ ↔ 2Zn2+. Indium and Sn are mainly present in Sp-I and Sp-III. Chalcopyrite contains Zn and Sn both exceeding 100 ppm. Contents of Se, Ag, In, and Sn in chalcopyrite are significantly higher than those in sphalerite. Calculation of the sphalerite trace element geothermometer (GGIMFis) suggests that the average sphalerite ore-forming temperatures are 164 °C (Sp-I), 156 °C (Sp-II), and 205 °C (Sp-III), implying medium- to low-temperature mineralization. This indicates a possible influx of high-temperature, in-bearing fluid during the late-stage mineralization.In summary, the faults-controlled vein-type Pb-Zn deposits (e.g., Xinhua) may have been products of the same Kwangsian orogeny as other strata bound MVT deposits, and the Xinhua deposit features two mineralization stages with multiple ore metal sources. During the ore-forming fluid ascent, some ore-forming materials may have precipitated in the fluid conduits. And exposed after the erosion of the shallower stratiform orebodies and strata. Consequently, the Xinhua Pb-Zn deposit represents the preserved ore-fluid conduit phase (in the basement strata) of the MVT mineralization.

Experiment on selective dynamic extraction of germanium by ultrasonic enhanced N235 extraction resin under complex system

Germanium plays an irreplaceable role in the field of modern high-tech materials and is an important strategic metal resource. N235 extraction resin was used to selectively extract [Ge(C4O6H4)3]2-. Under the condition of ultrasonic power at 120 W in a water bath, the extraction rate of germanium was 97.32%. The extraction rate of zinc was 2.37% under the conditions of a three-stage solid phase extraction column in series (single-stage filling N235 extraction resin 0.8 g), reaction temperature 25 °C, tartaric acid concentration of 2.0 g/L, and the dwell time is 4.1min. The saturated adsorption capacity of the resin is 51.90 mg/g. The extraction rate of germanium increased by 14.4% under ultrasonic-assisted strengthening conditions. The [Ge(C4O6H4)3]2- can be separated from the resin by NaOH solution. The desorption rate of germanium was 94.12% under the condition of water bath ultrasonic power of 120W, 30 ml concentration of 3.5 mol/L NaOH solution, and the dwell time is 5.2min. Under the optimum conditions, the extraction rate of N235 extraction resin was 85.23% after repeated regeneration five times. The results demonstrate that the extraction resin exhibits high selectivity and reproducibility in complex systems, presenting a new method for extracting germanium under complex conditions.

Selective electrosorption of silver ions from wastewater by biomass-derived N, S co-doped hierarchical porous carbon

The recovery of precious silver (Ag) from wastewater, a dual pursuit of environmental sustainability and economic benefits, faces a formidable challenge in the selective extraction of Ag+ ions amidst a matrix of other metal ions. To address this, we developed a novel N, S co-doped hierarchical porous carbon (NSPC) derived from a renewable precursor of Camellia oleifera shell. As the electrode material for capacitive deionization (CDI), the NSPC exhibited a high electrosorption capacity of 480.5 mg g−1 for Ag+ ions under an operating voltage of 1.2 V. Owing to the strong reaction between Ag+ and S functional groups and the synergistic effect from a hierarchical porous structure and N doping, the formation of Ag2S and elemental Ag is facilitated, and the NSPC cathode could selectively remove nearly 100 % of Ag+ ions from saline water and a solution containing Ni2+, Co2+, Pb2+, Zn2+, and Fe3+ ions. Furthermore, the NSPC cathode showed a high anti-interference ability in the presence of anions (C10H14N2O82−, C4H4O62−, C5H7O5COO− and HCO3−) and excellent reusability until 9 cycles. The impressive results show that the biomass-derived NSPC has the potential for rapid and selective recovery of silver from wastewater and offers a solution for environmental remediation and metal resource recovery.

The prenatal assimilation of minerals and metals in nestlings of a small passerine bird

Although certain metals can reach their highest concentrations in tissues of newly hatched nestlings, their sources have yet to be fully elucidated. Evidence for the differentiation of body reserves, including some chemical elements, during avian embryonic life and early post-hatching period is limited mostly to studies on poultry. Here, we present novel findings on the bioaccumulation and egg-to-nestling transfer of 10 minerals and metals, including non-essential potentially toxic chemical elements (Cu, Ni Cd, Pb, Zn, Ag, Mg, Fe, Co and Ca) in the tissues of the gastrointestinal tract (GT), whole body (WB) and carcass (CA) of nestlings of a small passerine bird, the Eurasian Reed Warbler Acrocephalus scirpaceus, breeding in an intensively fertilized fishpond habitat. Our findings show that concentrations of metals that are relevant to contaminated systems (Cu, Ni, Cd, Pb, Zn, Fe and Co) are the highest in GT tissues across all the nestling age classes examined (from hatching to day 9 of life). The important question emerged from our findings: why the hatchlings were characterized by higher metal concentrations in GT, WB and CA compared to older nestlings. We suggest that the prenatal accumulation of chemical elements assimilated from egg contents, and their subsequent utilization for building various tissues/internal organs by the growing embryo, is a reasonable explanation for this finding. More specifically, the potential functional mechanism explaining the highest concentrations of some trace metals in hatchlings seems to be associated with an extremely high rate of utilization of residual yolk metal resources that survived from the embryonic until the post-natal period. On the basis of our own work and literature data, we identified a presumable significant discrepancy in the actual rate of egg-to-nestling and egg-to-embryo metal transfer due to the eggshell being ignored (a commonly occurrence), and only the egg contents being treated as the basic repository of chemical elements for developing embryos. Much more research is needed on the prenatal assimilation and subsequent accumulation of chemical elements in a developing avian embryo, representing both the transition from near-to-hatching embryos to hatchlings, and then to older nestlings.

Bronze technology and metal resources in the Zhouyuan area before and after the replacement of Shang and Zhou Dynasties

Bronze technology and metal resources in the Zhouyuan area before and after the replacement of Shang and Zhou Dynasties

Digitalization of the economy and sustainability of metallic mineral production

Due to the adverse impacts of climate change on the environment and biodiversity, sustainability has become a critical issue. This paper investigates the impact of digitalization on the sustainability of metallic mineral production, particularly CO2 emissions, within the Regional Comprehensive Economic Partnership (RCEP). Using data from 1998 to 2020 and the cross-sectional FMOLS technique, the study finds that a 1% increase in ICT investment reduces CO2 emissions by 0.32%, and a 1% rise in Internet access decreases emissions by 0.28%. However, electrification increases emissions due to higher energy demand and fossil fuel reliance. Economic growth and metallic resource trade volume also elevate emissions. Policy recommendations include smart urban development, sustainable rural electrification, fostering internet access, and implementing green logistics in metallic production trade to enhance sustainability in RCEP countries.

Unusual cobalt behaviors and enrichment in cobalt-rich crust from the Magellan seamounts in the Western Pacific

Marine cobalt-rich (Co-rich) crusts are submarine critical metal resources with high economic value. In this study, detailed in-situ fine-scale morphological, mineralogical, and geochemical analyses were conducted on Co-rich crust from the Western Pacific. The Co-rich crust can be divided into three layers: (1) Layer 1 is the oldest anthracite layer and contacts with the substrate, showing a very dense laminated/columnar texture. Layer 1 can be further divided into two distinct sublayers: a lower black, massive, dense sublayer (Layer 1–1) and an upper black-to-brown sublayer (Layer 1–2). (2) Layer 2 is porous and locally vuggy, and its pore space is filled with a large amount of silicate detrital minerals and clay minerals. (3) Layer 3, on the top, is black and dense, with a dendritic, columnar/laminated texture. Co is very unevenly distributed throughout the whole crust, with three distinct Co-rich areas. Layer 3 is a typical hydrogenetic crust and has not undergone late alteration. The main processes for Co enrichment are specific adsorption-oxidation on Mn-oxides and the structural incorporation of Co3+ into Mn-oxide phases. The average Co content of the Layer 3 is much higher than that of the other two layers. The presence of abundant detrital and clay minerals, along with high levels of Al, Si, and Ti in Layer 2, indicates the incorporation of terrigenous material, resulting in a high average growth rate. However, these processes are not conducive to Co enrichment. In the phosphatized Layer 1, fluctuations in element content are significantly greater than in the upper, non-phosphatized layers. Phosphatization has resulted in the partial decomposition of the initial Co-rich micro-layers, which may have reactivated and migrated Co, contributing to secondary Co enrichment.

Life cycle environmental trade-off of decarbonising UK industrial clusters — A cradle to gate approach

The industrial sector is a major source of greenhouse gas (GHG) emissions due to process emissions and a heavy reliance on fossil fuels for heat and power. Methods exist to produce low carbon versions of products made in industrial clusters, including hydrogen, carbon capture and storage and alternative production methods, but these could increase burdens to other areas of the environment, such as resource depletion and water scarcity. This study compares different decarbonisation pathways for ammonia, cement, methanol and steel produced in the UK, to determine whether decarbonising could result in unintended environmental consequences. To determine this, life cycle assessment was applied to compare 267 different pathways to the conventional (fossil fuel) baseline. We find that most pathways lead to GHG emission reductions (43 to 78 % on average) but would increase impacts to other areas of the environment, including metal resources and ecotoxicity (8 % to 5-fold and 19 % to 24-fold, on average respectively). This study is the first to assess decarbonisation pathways for unintended environmental impacts and is of interest to industry, policy makers and anyone modelling industrial lifecycle emissions.