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Consolidates the many different chemistries being employed to provide environmentally acceptable products through the upstream oil and gas industry.-- Provided by publisher.

Desalination and industrial plants all around the world generate large amounts of saline wastewater (brine). The discharge of brine from facilities poses a severe environmental threat, while at the same time, the opportunity to recover resources is being lost as discharged brine is rich in valuable metals that could be recovered as salts/minerals. To this aim, this study presents and analyzes for the first time the characteristics of different brine effluents (from industries such as desalination, oil and gas production, petrochemical, aquaculture, pharmaceutical, textile) to prevent environmental pollution and to recover valuable resources (i.e., salts, minerals, metals, chemicals) enabling the concept of waste-to-resource (circular water economy model). The results revealed that the common salinity values in brine effluents range from 0.5 to 150 g/L, while the only exception is the produced water from the oil and gas industry (up to 400 g/L). Brine effluents from all sectors contain sodium, chloride, calcium, and potassium ions in high concentrations, while the production of common salts such as NaCl, CaCl 2 , and MgCl 2 from brine can be economically profitable. Besides common ions, precious metals such as lithium, rubidium, and cesium are present in low concentrations (<25 mg/L); however, their extraction from brine effluents can be significantly profitable due to their very high sale price. The treatment and valorization of brine can be implemented by the hybridization of membrane-based, chemical, biological, and thermal-based technologies/processes in minimal and zero liquid discharge (MLD/ZLD) systems. Graphical abstract

Proper disposal of industrial brine has been a critical environmental challenge. Zero liquid discharge (ZLD) brine treatment holds great promise to the brine disposal, but its application is limited by the intensive energy consumption of its crystallization process. Here we propose a new strategy that employs an advanced solar crystallizer coupled with a salt crystallization inhibitor to eliminate highly concentrated waste brine. The rationally designed solar crystallizer exhibited a high water evaporation rate of 2.42 kg m −2 h −1 under one sun illumination when treating real concentrated seawater reverse osmosis (SWRO) brine (21.6 wt%). The solar crystallizer array showed an even higher water evaporation rate of 48.0 kg m −2 per day in the outdoor field test, suggesting a great potential for practical application. The solar crystallizer design and the salt crystallization inhibition strategy proposed and confirmed in this work provide a low-cost and sustainable solution for industrial brine disposal with ZLD. Proper disposal of industrial brine remains a critical environmental challenge. Here, the authors devise a solar crystallizer and propose a salt crystallization inhibition strategy, which together provide a low-cost and sustainable solution for industrial brine disposal with zero liquid discharge.

Lithium-aluminum layered double hydroxides (LiAl-LDH) have been be successfully applied in commercial-scale for lithium extraction from salt lake brine, however, further advancement of their applications is hampered by suboptimal Li+ adsorption performance and ambiguous extraction process. Herein, a doping engineering strategy was developed to fabricate novel Zn 2+ -doped LiAl-LDH (LiZnAl-LDH) with remarkable higher Li + adsorption capacity (13.4 mg/g) and selectivity (separation factors of 213, 834, 171 for Li + /K + , Li + /Na + , Li + /Mg 2+ , respectively), as well as lossless reusability in Luobupo brine compared to the pristine LiAl-LDH. Further, combining experiments and simulation calculations, it was revealed that the specific surface area, hydrophilic, and surface attraction for Li + of LiZnAl-LDH were significantly improved, reducing the adsorption energy ( E ad ) and Gibbs free energy (ΔG), thus facilitating the transfer of Li + from brine into interface followed by insertion into voids. Importantly, the intrinsic oxygen vacancies derived from Zn-doping depressed the diffusion energy barrier of Li + , which accelerated the diffusion process of Li + in the internal bulk of LiZnAl-LDH. This work provides a general strategy to overcome the existing limitations of Li + recovery and deepens the understanding of Li + extraction on LiAl-LDH.

The demand for lithium is growing rapidly with the increase in electric vehicles, batteries and electronic equipments. Lithium can be extracted from brines, yet the separation of lithium ions Li + from magnesium ions Mg 2+ is challenging at high Mg/Li ratios. Here, we review methods to extract lithium from brines, such as extraction, adsorption, nanofiltration, selective electrodialysis and electrochemical intercalation/de-intercalation, with focus on the selective separation of lithium at high Mg/Li ratios. Extraction can be done with organic solvents and ionic liquids. Adsorption is performed with aluminum-, manganese- and titanate-based adsorbents.

Background Climate change threatens Earth’s ice-based ecosystems which currently offer archives and eco-evolutionary experiments in the extreme. Arctic cryopeg brine (marine-derived, within permafrost) and sea ice brine, similar in subzero temperature and high salinity but different in temporal stability, are inhabited by microbes adapted to these extreme conditions. However, little is known about their viruses (community composition, diversity, interaction with hosts, or evolution) or how they might respond to geologically stable cryopeg versus fluctuating sea ice conditions. Results We used long- and short-read viromics and metatranscriptomics to study viruses in Arctic cryopeg brine, sea ice brine, and underlying seawater, recovering 11,088 vOTUs (~species-level taxonomic unit), a 4.4-fold increase of known viruses in these brines. More specifically, the long-read-powered viromes doubled the number of longer (≥25 kb) vOTUs generated and recovered more hypervariable regions by >5-fold compared to short-read viromes. Distribution assessment, by comparing to known viruses in public databases, supported that cryopeg brine viruses were of marine origin yet distinct from either sea ice brine or seawater viruses, while 94% of sea ice brine viruses were also present in seawater. A virus-encoded, ecologically important exopolysaccharide biosynthesis gene was identified, and many viruses (~half of metatranscriptome-inferred “active” vOTUs) were predicted as actively infecting the dominant microbial genera Marinobacter and Polaribacter in cryopeg and sea ice brines, respectively. Evolutionarily, microdiversity (intra-species genetic variations) analyses suggested that viruses within the stable cryopeg brine were under significantly lower evolutionary pressures than those in the fluctuating sea ice environment, while many sea ice brine virus-tail genes were under positive selection, indicating virus-host co-evolutionary arms races. Conclusions Our results confirmed the benefits of long-read-powered viromics in understanding the environmental virosphere through significantly improved genomic recovery, expanding viral discovery and the potential for biological inference. Evidence of viruses actively infecting the dominant microbes in subzero brines and modulating host metabolism underscored the potential impact of viruses on these remote and underexplored extreme ecosystems. Microdiversity results shed light on different strategies viruses use to evolve and adapt when extreme conditions are stable versus fluctuating. Together, these findings verify the value of long-read-powered viromics and provide foundational data on viral evolution and virus-microbe interactions in Earth’s destabilized and rapidly disappearing cryosphere. B3KUN5MJ8EAz4vqucsgZtL Video Abstract

Desalination plays a critical role in addressing global water scarcity, yet brine disposal remains a significant environmental challenge. This study evaluates a minimal liquid discharge (MLD) membrane-based system integrating high-pressure reverse osmosis (HPRO) and membrane distillation (MD) for brine treatment, with a focus on the Eastern Mediterranean. A techno-economic assessment (TEA) was conducted to analyze the system’s feasibility, water recovery performance, energy consumption, and cost-effectiveness. The results indicate that the hybrid HPRO-MD system achieves a high water recovery rate of 78.65%, with 39.65 m3/day recovered from MD and 39 m3/day from HPRO. The specific energy consumption is 23.2 kWh/m3, with MD accounting for 89% of the demand. The system’s cost is USD 0.99/m3, generating daily revenues of USD 228 in Cyprus and USD 157 in Greece. Compared to conventional brine disposal methods, MLD proves more cost-effective, particularly when considering evaporation ponds. While MLD offers a sustainable alternative for brine management, challenges remain regarding energy consumption and the disposal of concentrated waste streams. Future research should focus on renewable energy integration, advanced membrane technologies, and resource recovery through brine mining. The findings highlight the HPRO-MD MLD system as a promising approach for sustainable desalination and circular water resource management.

In this study, we conduct a statistical analysis using the 4-plot, visibility graph, and horizontal visibility graph methods on brine extraction data from the Salar de Atacama basin in Chile. The 4-plot reveals real trends in the data that could lead model proposals. Conversely, complex networks analysis yields no significant findings, suggesting that the data lacks internal structural features and appears random. This randomness underscores the decision-making processes and highlights areas for potential optimization.

NaCl-saturated brines such as saltern crystalliser ponds, inland salt lakes, deep-sea brines and liquids-of-deliquescence on halite are commonly regarded as a paradigm for the limit of life on Earth. There are, however, other habitats that are thermodynamically more extreme. Typically, NaCl-saturated environments contain all domains of life and perform complete biogeochemical cycling. Despite their reduced water activity, ∼0.755 at 5 M NaCl, some halophiles belonging to the Archaea and Bacteria exhibit optimum growth/metabolism in these brines. Furthermore, the recognised water-activity limit for microbial function, ∼0.585 for some strains of fungi, lies far below 0.755. Other biophysical constraints on the microbial biosphere (temperatures of >121°C; pH > 12; and high chaotropicity; e.g. ethanol at >18.9% w/v (24% v/v) and MgCl2 at >3.03 M) can prevent any cellular metabolism or ecosystem function. By contrast, NaCl-saturated environments contain biomass-dense, metabolically diverse, highly active and complex microbial ecosystems; and this underscores their moderate character. Here, we survey the evidence that NaCl-saturated brines are biologically permissive, fertile habitats that are thermodynamically mid-range rather than extreme. Indeed, were NaCl sufficiently soluble, some halophiles might grow at concentrations of up to 8 M. It may be that the finite solubility of NaCl has stabilised the genetic composition of halophile populations and limited the action of natural selection in driving halophile evolution towards greater xerophilicity. Further implications are considered for the origin(s) of life and other aspects of astrobiology.

Achieving high selectivity of Li + and Mg 2+ is of paramount importance for effective lithium extraction from brines, and nanofiltration (NF) membrane plays a critical role in this process. The key to achieving high selectivity lies in the on-demand design of NF membrane pores in accordance with the size difference between Li + and Mg 2+ ions, but this poses a huge challenge for traditional NF membranes and difficult to be realized. In this work, we report the fabrication of polyamide (PA) NF membranes with ultra-high Li + /Mg 2+ selectivity by modifying the interfacial polymerization (IP) process between piperazine (PIP) and trimesoyl chloride (TMC) with an oil-soluble surfactant that forms a monolayer at oil/water interface, referred to as OSARIP. The OSARIP benefits to regulate the membrane pores so that all of them are smaller than Mg 2+ ions. Under the solely size sieving effect, an exceptional Mg 2+ rejection rate of over 99.9% is achieved. This results in an exceptionally high Li + /Mg 2+ selectivity, which is one to two orders of magnitude higher than all the currently reported pressure-driven membranes, and even higher than the microporous framework materials, including COFs, MOFs, and POPs. The large enhancement of ion separation performance of NF membranes may innovate the current lithium extraction process and greatly improve the lithium extraction efficiency. Achieving high selectivity of Li+ and Mg2+ is of paramount importance for effective lithium extraction from brines, and nanofiltration (NF) membrane plays a critical role in this process. Here the authors report the fabrication of polyamide NF membranes with ultra-high Li + /Mg2+ selectivity by modifying the interfacial polymerization process with an oil-soluble surfactant.