Newswise — ALBUQUERQUE, N.M. —When Sandia scientists Ryan Davis and Nathan Bays set out to find a better way to absorb and degrade PFAS in water sources, they kept running into the same issue: Detecting the chemicals in samples took too long.

So, they came up with their own solution.

They’ve developed a faster, cheaper way to test for PFAS.

The problem of PFAS and solving it

PFAS, or per-and polyfluoroalkyl substances, are commonly called forever chemicals because they don’t break down naturally in the environment. They can move through soil and water and build up in wildlife and humans.

Ryan, a chemist, has spent years developing technologies that can eliminate PFAS on both large and small scales. But that research has been time-consuming. Depending on the concentration, it can take hours to days to detect PFAS in a single sample.

“A common complaint of ours and others who are doing PFAS analysis is that it’s slow and can be costly depending on the technology,” Ryan said.

Traditional testing processes requires repetitive extraction, concentration and processing.

 It starts with a liter or more of liquid, suspected to contain PFAS. The liquid is forced through a cartridge to extract the PFAS. The collected PFAS is then added to a smaller volume of water, and the process is repeated with new cartridges until enough PFAS concentrated for detection.  

The process is not only time-consuming but also costly. Cartridges can cost several hundred dollars apiece.

That process not only slows research and development but puts testing out of reach for the average person.

“We want a technology that can be broadly accessible, not only for researchers but for the broader public and government,” Ryan said. “It will allow regulators to track PFAS in the environment, and for people to test their own tap water.”  

A new way to detect PFAS

Ryan and Sandia postdoctoral researcher Nathan Bays have developed that technology.

The pair stumbled onto the approach while experimenting with a mass spectrometer and a technique called desorption electrospray ionization, or DESI. The process uses electrically charged droplets sprayed at the surface of an adsorbent that ionizes only the target chemical, not the adsorbent itself.

 Bays and Ryan said the results were unexpected.

“We had toyed with the idea of using DESI to confirm the presence of PFAS on adsorbent materials,” Ryan said. “When we did some preliminary testing, not only did we confirm the presence of PFAS, but we noticed that we got results well beyond our standard analysis.”

“At this point, it became very clear we had an opportunity to push further on this work,” Bays said. “One step at a time, we went from just being able to see PFAS at parts-per-million—to levels at parts-per-billion, and finally low parts-per-trillion.”

Ryan and Bays’ technique starts with an adsorbent about the size of a Rice Krispy. The adsorbent is placed in a solution for testing. Three minutes later, it is removed and placed in front of a mass spectrometer where it is sprayed with electrically charged droplets. The droplets remove PFAS from the adsorbent and carry it into the mass spectrometer, where it is analyzed for PFAS concentration and type.

The entire process can take as little as five minutes.

“It’s one of those outcomes that wasn’t exactly planned as we had initially envisioned it,” Ryan said. “It was surprising to see the concentration of PFAS so clearly. That may be why it hadn’t been done before. It was just unexpected.”

The pair has published details of the process in hopes it can be commercialized for widespread use. They also hope it can be developed to tackle other environmental pollutants besides PFAS and used for environmental analytics and testing such as off- gassing measurements tied to Sandia’s nuclear deterrence work.   

“It could help researchers understand the system’s environment and the off-gassing of chemicals in certain work,” Ryan said. “While our first phase worked with liquid, our more recent work has delved into the gas phase.”

Why they do it

Both Ryan and Nathan are passionate about this technology and PFAS remediation. Developing the new test is just a small part of the broader work they do aimed at reducing PFAS pollution.

“I’ve been working on this specific project since I joined Sandia two and a half years ago,” Nathan said. “My whole career has evolved around environmental remediation, so this was a natural fit. I’m a big outdoors person. My wife and I like to go out in nature, and we don’t like to see our world be polluted like this.”

One of the biggest focuses of PFAS remediation has been at U.S. Air Force bases, where soil and groundwater have been impacted by the long-term use of firefighting foam.

Ryan’s big goal, however, is to give people more power over their health. “More and more research shows that PFAS can have negative outcomes at even low concentrations, so detecting at those low concentrations is key,” Ryan said. “We don’t want families to worry about whether they can afford groceries this week or test their water for safety.”

Newswise — In a study published in Bioresource Technology Journal, scientists from the universities of Portsmouth and Manchester report that a specially engineered enzyme can significantly speed up the breakdown of PET – the plastic used in water bottles, food packaging and polyester clothing – when it is processed at high concentrations similar to those used in industry. 

PET, short for poly (ethylene terephthalate), is cheap, durable, and widely used. But those same qualities mean it builds up in vast quantities once thrown away. 

Polyester textiles are notoriously difficult to recycle. Their fibres are tightly packed and highly ordered into a structure created during manufacturing, which makes them resistant to biological breakdown. 

Enzymes are natural proteins that can speed up chemical reactions. The team combined two different components into one fusion enzyme. The first was a heat-tolerant cutinase; a natural enzyme that normally breaks down a protective polyester found on plant surfaces called cutin. The second was a binding module designed to help the enzyme to attach more tightly to plastic. 

The two components were carefully matched, so they work best at the same temperature and are suited to the same kinds of plastic structure. The aim was to make the enzyme stick to PET and ensure it could continue breaking it down efficiently under realistic recycling conditions. 

While the modified enzyme did attach more strongly to highly crystalline PET – the tough, tightly packed form found in many plastics – did not automatically lead to faster breakdown. In fact, when the plastic structure remained highly ordered, there was limited gain. 

The real progress came when the plastic was less crystalline and as a result more accessible to the enzyme. Under controlled conditions that mimic industrial recycling – including carefully managed pH and plastic concentrations of 20 per cent by weight – the fused enzyme broke down less-ordered PET much more quickly. 

The biggest improvement was seen in a pre-consumer polyester textile that had been specially treated to make it less crystalline and finely ground. In that case, the amount of useful breakdown products doubled. 

“By matching the enzyme with the right binding module and preparing the plastic in the right way, we can overcome a major bottleneck in plastic recycling,” said Professor Andrew Pickford, Director of the University of Portsmouth’s Centre for Enzyme Innovation (CEI). “This isn’t just about helping the enzyme stick to the surface – it’s about making sure the chemical reaction can run efficiently at the high plastic concentrations used in industry.” 

The findings also help explain why earlier studies of similar enzyme combinations have produced mixed results. If an enzyme binds too tightly to the surface, it can slow the reaction – a well-established concept in chemistry known as the Sabatier principle. 

The study suggests that enzyme-based recycling of PET – a promising but technically challenging solution – could become more practical at scale but success, depends on getting three factors right: the enzyme, any helper module that guides it to the plastic, and the structure of the material itself. 

Catalytic treatment of industrial pollutants has long faced a practical bottleneck. Noble metal nanoparticles are highly active, but they often tend to aggregate, reducing the number of active usable reaction sites. Traditional methods for producing polymer-supported catalysts can also be slow, multistep, and dependent on toxic reagents, surfactants, or poorly controlled batch conditions. Meanwhile, 4-nitrophenol remains a hazardous pollutant commonly found in industrial wastewater, and existing catalytic systems often suffer from limited surface area, uneven active-species distribution, and inefficient mass transfer. Based on these challenges, in-depth research is needed on controllable catalyst supports and continuous-flow catalytic platforms.

In a study published (DOI: 10.1038/s41378-026-01176-6) in 2026 in Microsystems & Nanoengineering, Li Ma and colleagues from Xi’an Jiaotong University and collaborating institutions reported a spiral-microchannel platform for continuously producing morphology-tailored polystyrene microspheres loaded with Ag, Ag-Au, or Ag-Pt nanoparticles. Corresponding author Nanjing Hao and the team showed that tuning the structure of the polymer carrier could directly improve catalytic behavior in the reduction of 4-nitrophenol.

The researchers began with uniform solid polystyrene seeds averaging 1.48 μm in diameter, then used water-ethanol and water-toluene systems to drive them into hollow, dimpled, bowl-like, and open-hole forms. In one striking transformation, unsymmetrical dimples evolved into open-hole structures within 5 minutes after introducing a small amount of toluene. These evolving microspheres were then passed through a spiral microreactor, where rapid microscale mixing enabled metal precursors to form and anchor onto the polymer surface in minutes rather than hours. Hollow and open-hole structures provided larger surface areas and confined microenvironments, helping load more nanoparticles and improve mass transfer. The system produced evenly distributed Ag, Ag-Pt, and Ag-Au nanoparticles, while also reducing aggregation. Among all tested catalysts, open-hole Ag-Pt microspheres performed best, reaching a reaction rate constant of 1.73 × 10^^-2 s^{^-1} and an activity parameter of 692 s^^-1·g^^-1, while maintaining catalytic activity over five reuse cycles.

The study suggests that catalyst performance can be engineered not only by changing the metal itself, but also by reshaping the support beneath it. By controlling carrier morphology, the team was able to regulate nanoparticle immobilization, improve accessibility of active sites, and strengthen confined synergistic catalysis. In this sense, the microreactor becomes more than a synthesis tool: it becomes a way to manufacture catalytic function with precision.

The implications go beyond a single wastewater reaction. A scalable continuous-flow strategy for robust bimetallic catalysts could be valuable in environmental remediation, fine chemical synthesis, and other industrial processes where fast mixing, stable active sites, and reusable catalytic materials are essential. Just as importantly, the study turns a toxic pollutant into a useful product, pointing toward a broader model of greener chemistry in which waste treatment and value creation can happen together.

###

References

DOI

10.1038/s41378-026-01176-6

Original Source URL

https://doi.org/10.1038/s41378-026-01176-6

Funding information

This work was supported by the National Key R&D Program of China (2023YFC3904301), the Key R&D Program of Shaanxi Province (2024GX-YBXM-471), the Qin Chuang Yuan Talent Program (2021QCYRC4-33), and the Distinguished Overseas Young Scholars of the National Natural Science Foundation of China (GYKP032).

About Microsystems & Nanoengineering

Microsystems & Nanoengineering is an online-only, open access international journal devoted to publishing original research results and reviews on all aspects of Micro and Nano Electro Mechanical Systems from fundamental to applied research. The journal is published by Springer Nature in partnership with the Aerospace Information Research Institute, Chinese Academy of Sciences, supported by the State Key Laboratory of Transducer Technology.

Newswise — UPTON, N.Y. — Mike Jensen, a meteorologist and interim chair of the Environmental Science and Technologies Department at the U.S. Department of Energy’s (DOE) Brookhaven National Laboratory, is a recipient of the DOE Distinguished Mentor Award for Workforce Development, a new award program that recognizes outstanding mentors from across DOE’s 17 national laboratories and their essential roles in developing STEM professionals.

Jensen is one of four mentors honored by DOE’s Office of Science for their excellence in guiding future scientists, engineers, and technical professionals through unique access to world-leading expertise, scientific user facilities, and research tools found at multidisciplinary national laboratories.

“The establishment of the DOE Distinguished Mentor Award for Workforce Development directly aligns with our strategic objectives to not only recognize exceptional mentorship but also to actively cultivate best practices across our National Laboratories,” said DOE Under Secretary for Science Darío Gil. “By illuminating these exemplary efforts, we reinforce a vibrant mentoring ecosystem crucial for advancing the DOE’s mission and strengthening the U.S. workforce. We look forward to celebrating our inaugural awardees and hearing their insights and experiences.”  

The mentors will be celebrated at a virtual ceremony later this year. Each awardee will receive $10,000 to be used for research and mentoring-related development.

Over the years, Jensen has mentored dozens of students — from high schoolers to graduate-level researchers — through programs supported by DOE’s Office of Science and Brookhaven Lab. His mentees have participated in DOE programs such as Science Undergraduate Laboratory Internships (SULI), Office of Science Graduate Student Research, the Workforce Development for Teachers and Scientists Pathway Summer Schools, and various Brookhaven pre-college offerings such as the High School Research Program (HSRP).

“I’m honored and humbled to be awarded,” said Jensen, who leads his department’s Cloud Processes and Measurement Group and is a principal investigator for the Atmospheric System Research (ASR) program’s Process-level AdvancementS of Coupled Cloud and Aerosol LifecycleS (PASCCALS) Science Focus Area and an active participant with the Atmospheric Radiation Measurement (ARM) User Facility, a multi-laboratory, DOE scientific user facility. “I consider mentorship an important part of my job as a scientist to help with the next generation, and I enjoy that part. It’s nice to be rewarded for something that I like doing.”

In his scientific work, Jensen collects data in the field to analyze and better understand the processes that drive the evolution of cloud systems and their role in the water cycle and the Earth’s energy balance. In field campaigns such as the TRacking Aerosol Convection interactions ExpeRiment, he and the ARM facility team deploy advanced atmospheric instruments to measure cloud structure, precipitation, and radiation.

Through Jensen’s mentorship, students see what atmospheric science looks like in practice. They learn about tools used in the field, such as radars and weather balloons, analyze datasets using coding and visualization tools like Python, and participate in exciting moments when new insights emerge from their data.

Jensen’s mentorship goes beyond helping students leave internships with new skills in data science and experimental analysis, said Aleida Pérez, manager of Brookhaven’s Office of Workforce Development and Science Education.

“He makes sure students are engaged with the broader network of atmospheric science researchers, helping them understand the impact of the research they collaborate on and see themselves as part of the research community,” Pérez said.

Jensen said he and his colleagues encourage students to embrace trial-and-error, whether they’re trying out ideas for experiments or exploring career pathways.

“We talk to them a lot about not being fearful of the research they’re doing and to go ahead and try new things,” Jensen said.

Those who nominated Jensen for the DOE award cited his accessibility, patience, and ability to instill confidence in aspiring scientists.

“To say that Mike had an impact on my life and career would be a severe understatement,” said Diana Apoznanski, a mentee of Jensen’s through HSRP and SULI. “Mike molded a timid high school student who had an interest in weather into a confident Ph.D. candidate studying Earth system modeling and impacts, and he has consistently and enthusiastically supported my career for an entire decade.”

Apoznanski is now pursuing a Ph.D. in atmospheric science at Rutgers University.

Jensen has also served as a mentor to new mentors, inspiring early-career researchers in his department to step into mentoring roles, Pérez said.

“He has supported his colleagues by serving as a co-mentor, providing guidance, and sharing what he has learned from collaborating with many students who have continued in STEM fields,” Pérez said.

Brookhaven National Laboratory is supported by the Office of Science of the U.S. Department of Energy. The Office of Science is the single largest supporter of basic research in the physical sciences in the United States and is working to address some of the most pressing challenges of our time. For more information, visit science.energy.gov.

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Newswise — By comparing natural microbial adaptation with targeted bioaugmentation using an antibiotic-degrading strain, the study reveals how biodegradation capacity fundamentally reshapes microbial succession, stability, and resilience under sustained antibiotic exposure.

Environmental risk assessments often judge antibiotics solely by concentration and intrinsic toxicity, assuming uniform microbial responses. However, microbial communities actively shape contaminant fate, particularly when they include antibiotic-degrading organisms. Sulfamethoxazole (SMX), a common sulfonamide found in wastewater and surface waters, illustrates this complexity. Even at low levels, SMX can suppress sensitive taxa, disrupt community structure, and impair essential functions such as nutrient removal. Yet some bacteria possess specialized genes that enzymatically inactivate SMX, reducing antibiotic pressure for the broader community. How such biodegradation capacity governs microbial succession and community stability remains insufficiently understood.

A study (DOI:10.48130/biocontam-0025-0016) published in Biocontaminant on 12 December 2025 by Bin Liang’s team, Harbin Institute of Technology, demonstrates that antibiotic-degrading bacteria act as keystone protectors that mitigate antibiotic stress, stabilize microbial community succession, and enhance ecosystem resilience, highlighting biodegradation capacity as a critical determinant of environmental risk.

Using a controlled sequencing batch reactor framework, the study first isolated and characterized an SMX-degrading bacterium from activated sludge by continuous subculture with SMX as the sole carbon source, then tested how degrader-enabled biodegradation reshapes community succession by inoculating the strain under defined antibiotic stress and tracking community dynamics with SMX degradation assays, ex situ degradation tests, and 16S rRNA sequencing across multiple reactor phases. The isolated strain, Paenarthrobacter sp. M5 (100% 16S rRNA similarity to P. ureafaciens), fully degraded 30 mg/L SMX within 10 h, producing equimolar 3-amino-5-methylisoxazole and carrying the key gene sadA; mechanistically, a SadA/SadC two-component system drove ipso-hydroxylation and cleavage of the -C–S–N- bond, yielding non-antibacterial intermediates (including p-aminophenol that could be further metabolized for growth). Four reactor treatments were established—NN (no SMX), SN (natural adaptation with SMX), NM (M5 inoculated without SMX), and SM (pre-adaptation: M5 inoculated with SMX)—revealing that SN communities acquired biodegradation gradually (over ~28 cycles at 2 mg/L SMX), whereas SM communities showed immediate, efficient degradation after inoculation; with increasing SMX loads, both SMX-exposed groups ultimately achieved complete removal, indicating inducible biodegradation under sustained selection. When SMX exposure was paused and then reintroduced at high levels, functional recovery ranked SN > SM > NM, while NN showed ~70% degradation with high replicate variability, underscoring how evolutionary history governs resilience. Ex situ assays reinforced these trends: SN improved to 36.3%, 62.3%, and 100% removal at 2, 5, and 10 mg/L SMX, SM remained consistently complete across phases, NN stayed low (12.2%–16.6%), and NM declined (30.5%→13.4%), highlighting antibiotics as the key driver sustaining degrader colonization. 16S/OTU analyses showed a shared core microbiome across all groups, but shared OTUs dropped sharply during restructuring (from 1,035 to ~440) before stabilizing (~533–578), while α-diversity patterns revealed that slower biodegradation in SN retarded succession and preserved higher diversity during T2–T4, whereas efficient degradation in SM buffered antibiotic stress and restored “regular” successional dynamics. Multivariate statistics (ADONIS/MRPP) confirmed dose-dependent SMX-driven divergence in SN versus NN, but minimal structural differences between SM and NN through most phases, indicating that bioaugmentation-mediated biodegradation can protect community structure from antibiotic perturbation.

These findings have direct relevance for wastewater treatment and environmental management. Antibiotic-degrading bacteria can stabilize treatment performance by protecting key microbial functions from antibiotic disruption. Targeted bioaugmentation or monitoring of native degrader populations could reduce the risk of treatment failure and limit conditions that favor the spread of antibiotic resistance.

###

References

DOI

10.48130/biocontam-0025-0016

Original Source URL

https://doi.org/10.48130/biocontam-0025-0016

Funding Information

The study was funded by the National Natural Science Foundation of China (Grant No. 52322007), the Guangdong Basic and Applied Basic Research Foundation (Grant No. 2023B1515020077), and Shenzhen Science and Technology Program (Grant No. JCYJ20240813105125034).

About Biocontaminant

Biocontaminant is a multidisciplinary platform dedicated to advancing fundamental and applied research on biological contaminants across diverse environments and systems. The journal serves as an innovative, efficient, and professional forum for global researchers to disseminate findings in this rapidly evolving field.

Newswise — Algae blooms make a pond’s surface shine in mesmerizing green hues. But if the microorganisms responsible are cyanobacteria, they can also release toxins that harm humans and wildlife alike. So, a team reporting in ACS ES&T Water has designed a “set it and forget it” system for distributing algaecide using specialized buoys tethered at the site of a bloom. In tests, the buoys removed nearly all cyanobacteria without the need for frequent reapplication.

Algae blooms occur when extra nutrients in the water — likely from fertilizer runoff — cause tiny microorganisms like algae and cyanobacteria to proliferate. In 2014, one such algae bloom in Lake Erie near Toledo, Ohio, rendered drinking water unsafe for hundreds of thousands of residents. And now, a team of researchers from the University of Toledo are looking to create an algaecide treatment system that puts a stop to a bloom before it has even started. The team, including Umberto Kober, Hanieh Barikbin, Youngwoo Seo, Yakov Lapitsky and colleagues, designed a system that releases algaecide steadily over a period of weeks or months, making it less expensive and more efficient than existing options that require frequent reapplication.

The team constructed small, medium, and large-sized buoys out of PVC pipes, forming either a “T” or cross shape. Hydrogel disks were inserted into the pipe openings to control the diffusion of the liquid algaecide into the surrounding water. The buoys were then filled with a commercial hydrogen peroxide-based algaecide, which, upon immersion, slowly diffused through the hydrogel disks. The buoys were also engineered so that once the algaecide was gone, the buoy fell to its side, visually indicating that a refill was needed.

To test their performance, the small, algaecide-loaded buoys were put in a beaker with 1 liter of cyanobacteria-containing water collected from Lake Erie and monitored for two weeks. Every day a small portion of water was replaced with new lake water to ensure the buoys were continually exposed to fresh cyanobacteria. This way, the team could evaluate whether the buoys provided sustained algicidal activity rather than killing the cyanobacteria early in the process. Researchers found that the cyanobacteria were almost entirely eliminated within a week, and other microbes remained largely unscathed. Researchers estimate that their buoys could reliably release algaecide for at least four consecutive release cycles, each lasting 35 days.

Though further research is needed, including enhancements to prevent microbe growth on the buoy’s surface, the researchers say that this work overcomes challenges in sustained and targeted algaecide treatment.

“If successfully scaled up, this concept could enable early mitigation of harmful algal blooms without the need for labor-intensive repeated algaecide applications,” says Lapitsky.

The authors acknowledge funding from the U.S. Army Corps of Engineers. The algaecide used in these experiments was provided by the SePRO Corporation, an algaecide manufacturer.

Authors Yakov Lapitsky, Umberto Kober and Youngwoo Seo have filed a patent application on this research.

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Newswise — Labeled glass containers full of liquids stirred by spinning magnets are connected to humming machines with neatly organized tubes. Here in this lab space at the Idaho National Laboratory (INL), scientists are pioneering ways to extract critical materials from recycled waste products.

Critical materials are essential to modern life because they possess properties that make them difficult to replace. They’re used in smartphones, satellites, computer chips, rechargeable batteries, fighter jets, advanced weapons systems and other technologies. But they can be hard to find; that’s where INL’s research comes in.

The national challenge

The U.S. has deposits of nearly all critical materials, but mining capabilities cannot meet the nation’s growing demand. Most extraction and processing are done overseas, much of it in China. This reliance on foreign critical materials risks supply disruptions that could affect U.S. national security, economic growth and everyday life. After mining, rocks are crushed and processed to separate valuable materials from waste. This step, called beneficiation, prepares the material for further refining. These materials are then concentrated for easier transport and treated with heat or chemicals to fully extract and purify them. However, modern processing isn’t always sufficient and often produces significant waste.

In copper mines, for example, the ore contains up to 0.2% copper, meaning about 99.8% of the rock is discarded. That waste still contains other metals and critical materials, but most processing facilities are only designed to extract one or two materials.

The critical materials in discarded rocks, e-waste and other sources don’t degrade over time and can be recovered. However, the U.S. lacks the infrastructure to recycle them.

Recycling facilities could tap into these largely untouched sources, helping meet U.S. demand. These facilities could be built far more quickly than new mines, which can take over a decade due to permitting, costs and infrastructure needs.

“The U.S. doesn’t recycle well,” said Bob Fox, a senior manager at INL. “There’s a willingness to recover critical materials from recycled sources, but there’s no infrastructure or market for it. Right now, critical materials recycling doesn’t have the economic incentives to drive infrastructure development.”

INL is working to change that by making recycling more efficient, less energy-intensive and economically viable.

“Recycling represents a crucial pathway for the U.S. to obtain critical materials, including rare earth elements like dysprosium,” said Arindam Mukhopadhyay, a staff scientist at INL. “Even critical materials we mine domestically, such as lithium, cobalt, nickel and manganese, can be recovered through recycling.”

INL’s recycling research

Since the early 2010s, INL has developed technologies that reduce chemical use, energy consumption and waste, making recycling more sustainable and cost-effective. These innovations improve recovery from sources such as electronic and agricultural waste, mine tailings and industrial wastewater.

“INL has developed a comprehensive portfolio of critical materials recycling technologies,” said Mukhopadhyay. “We have the expertise and proven processes to help make recycling economically competitive, which is essential for building a reliable domestic supply of the materials our nation depends on.”

One area INL has worked in for many years is biohydrometallurgy, which uses biological systems to dissolve and recover metals. INL’s research examines how microbial populations fed agricultural or municipal waste biomass produce organic acids that break down metals in both metallic and mineral forms. These biologically produced acids dissolve the material and release valuable metals such as rare earth elements, cobalt and lithium. The dissolved metals can then be recovered from the liquid using natural biology-based molecules instead of man-made chemicals. INL’s work is improving the efficiency, effectiveness and affordability of biohydrometallurgy and offers a promising, cost-effective alternative to harsh chemical reagents.

Ether-based Aqueous Separation and Extraction (EASE) uses water-soluble, ether-based chemicals that pull specific materials from mixtures to recover critical materials from industrial wastewater, desalination brines, mine runoff and geothermal fluids. This process uses less energy and fewer chemicals than conventional extraction methods and produces less waste.

Another area of innovation is INL’s electrochemistry work. Electrochemistry uses electricity to trigger chemical reactions that separate and recover critical materials from waste.

Electrons are easier and less expensive to generate than the chemicals required for traditional extraction methods. Electrochemistry can reduce the use of chemicals, some of which can be toxic, by 88% to 90%, and the process uses up to 75% less energy.

Electrochemical Leach (EC-Leach)

EC-Leach uses electricity to cause chemical reactions in liquids to extract critical materials like lithium, cobalt, nickel and manganese. The process was originally developed to extract critical materials from used lithium-ion batteries, but INL is adapting it for mining applications.

Pilot systems show EC-Leach can recover more than 95% of these critical materials. INL researchers are working to scale this technology for commercial deployment.

Electrochemical Recycling of Electronic Constituents of Value (E-RECOV)

E-RECOV uses an electrochemical cell to recover critical materials from electronic scrap. Electrochemical cells use chemical reactions to produce electricity used in electrochemistry. E-RECOV operates at room temperature, uses up to 75% fewer chemicals than traditional processes and doesn’t produce toxic emissions.

The technology has received a TechConnect National Innovation Award and was a finalist for an R&D 100 Award. The U.S. Department of Energy’s Critical Materials Institute supports the development of TechConnect.

Free Flowing Electrophoretic System (FFES)

The FFE unit uses an electric field with tailored ligand systems (small molecules that bind to metal ions) to separate critical materials from complex mixtures into distinct, isolated streams. The device can be moved closer to, or into, mines to separate critical materials from metal-rich liquids.

Electrochemical Membrane Reactor

Researchers at INL developed an electrochemical membrane reactor that removes contaminants from spent lithium-ion battery leachates, the mineral-rich liquids produced during recycling. The reactor recovers more than 95% of valuable metals such as nickel and cobalt using only water, air and electricity. It also produces acid that can be reused in the extraction process. The system has the potential to serve as a cost-effective closed-loop solution for recycling critical materials from batteries.

Improving purity

Most modern applications need critical materials to be at 99.999% purity or higher, but most conventional separation processing can only achieve 85% to 95% purity unless the process is run over weeks or months. INL’s electrochemical work can achieve 99.9999% purity in fewer cycles, dramatically reducing processing time and costs.

Rare Earth Element-Metal (RE-Metal)

RE-Metal is a process that recovers rare earth elements from waste materials using electricity. First, the elements are dissolved using nontoxic solutions. Then an electric current is applied to turn the dissolved materials into solid metal on an electrode.

Other projects include generating hydrogen peroxide from air to help dissolve minerals and separating graphite, copper and arsenic while immobilizing toxic chemicals.

Real-world impact

“Our goal is to make recycling economically viable,” said Mukhopadhyay. “To do that, we’ve focused on reducing chemical use, energy consumption and waste generation while maximizing recovery rates.”

INL’s technologies offer cost-effective options to secure the domestic critical materials supply chain and meet the nation’s growing demand. By advancing recycling and recovery methods, INL helps ensure the U.S. has the materials it needs to overcome current and future challenges.

About Idaho National Laboratory

Battelle Energy Alliance manages INL for the U.S. Department of Energy’s Office of Nuclear Energy. INL is the nation’s center for nuclear energy research and development, and also performs research in each of DOE’s strategic goal areas: energy, national security, science and the environment. For more information, visit www.inl.gov.

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Newswise — University of Utah professors Hilary Coon, PhD, David Grunwald, PhD, and Chris Hill, DPhil, have been elected by the Council of the American Association for the Advancement of Science as AAAS Fellows. This prestigious lifetime honor recognizes scientists who have advanced their fields through research, leadership, or mentorship.

Hill, Grunwald, and Coon are among nearly 500 scientists, engineers, and innovators who have been elected 2025 Fellows for their scientifically and socially distinguished achievements throughout their careers.

“The election of Drs. Coon, Grunwald, and Hill reflects the lifetime of outstanding work that they have contributed to their scientific fields as researchers, leaders, and collaborators,” says Rachel Hess, MD, MS, Associate Vice President for Research at U of U Health. “They are key members of our Utah community, and we are so excited for them to receive this recognition.”

Hilary Coon

Coon, Benning Endowed Presidential Professor of psychiatry and researcher at Huntsman Mental Health Institute, studies the complex genetic and environmental factors that contribute to psychiatric conditions.

Her research currently focuses on a large population-based study of risks leading to suicide mortality which she developed over a span of two decades. This study has begun to reveal clinical, demographic, and genetic changes that are linked to suicide risk. By better identifying who’s at risk, Coon’s research opens the door to targeted interventions and new treatments to save lives. Her work has also spanned studies focused on other psychiatric conditions and complex medical disorders. 

Newswise — The marginal ice zone marks the boundary between open ocean and sea-ice cover and represents one of the most dynamic environments in polar oceans. Ocean eddies generated near ice edges influence sea-ice transport, mixing processes, and energy exchange between the ocean and atmosphere. These rotating structures can redistribute floating sea ice, modify heat transport, and affect regional ecosystems and climate feedback mechanisms. However, direct observations of eddy evolution remain limited because of harsh polar conditions and sparse in-situ measurements. Satellite synthetic aperture radar (SAR) has become an important tool for detecting eddies through sea-ice patterns, yet most previous studies mainly analyzed spatial distributions rather than the dynamic evolution of individual eddies. Because of these challenges, deeper investigation of the spatiotemporal evolution of ice-edge eddies is required.

Researchers from the Aerospace Information Research Institute of the Chinese Academy of Sciences reported a new framework for analyzing the evolution of ice-edge eddies using sequential SAR satellite imagery. Their findings were published (DOI: 10.34133/remotesensing.1031) on March 2, 2026, in the journal Journal of Remote Sensing. The study focuses on an eddy observed in the Fram Strait, a key passage connecting the Arctic Ocean and the North Atlantic. By integrating sea-ice motion tracking with hydrodynamic vortex modeling, the researchers quantified key physical characteristics of the eddy, including rotational velocity, circulation strength, and radius, providing new insight into polar ocean dynamics.

The study introduces a dynamical parameter inversion framework capable of reconstructing the structure and temporal evolution of ice-edge eddies. Using sequential SAR images, the researchers tracked the displacement of floating sea ice to derive high-resolution surface current fields. These currents were then analyzed using a vortex-based hydrodynamic model to estimate key parameters such as suction intensity, angular velocity, and circulation strength.

Applying the framework to an Arctic eddy revealed a complete life cycle lasting about 22 days. During the early stage, the eddy gradually intensified as both its radius and circulation strength increased. The vortex reached a mature phase when its structure became most coherent and energetic. Afterward, the eddy weakened and gradually dissipated. The results demonstrate how polar ocean eddies evolve dynamically and provide quantitative evidence of their growth, maturity, and decay processes. The research focused on the Fram Strait, where complex interactions between the southward-flowing East Greenland Current and the northward-flowing West Svalbard Current frequently generate ocean eddies. Researchers analyzed time-series SAR images collected by the Sentinel-1A and Sentinel-1B satellites, which provide high-resolution radar observations capable of monitoring sea-ice patterns regardless of cloud cover or lighting conditions. To reconstruct eddy dynamics, the team first tracked the displacement of floating sea ice between consecutive SAR images separated by roughly 50 minutes, allowing them to retrieve the horizontal surface current field associated with the eddy. The retrieved currents were then processed using singular value decomposition to isolate the dominant rotational component while suppressing background currents and noise.

Next, the Burgers–Rott vortex model—derived from the Navier–Stokes equations—was applied to invert the dynamical parameters describing the eddy. Analysis showed that the eddy radius expanded from roughly 28 km to over 35 km, while circulation strength peaked at about 4.5 × 10⁴ m²/s. The reconstructed current fields closely matched satellite-derived observations, confirming the reliability of the proposed method for capturing real ocean dynamics.

The researchers emphasized that ice-edge eddies are crucial components of polar ocean circulation. “These eddies strongly influence sea-ice redistribution and ocean mixing in Arctic waters,” the team explained. By enabling continuous monitoring of eddy evolution using satellite radar imagery, the new framework provides a valuable observational tool for studying ocean–ice interactions and improving understanding of polar climate dynamics.

The framework integrates satellite remote sensing with physical modeling techniques. Sequential SAR images were first preprocessed through radiometric calibration, filtering, and image registration. The displacement of floating sea ice between image pairs was calculated using a maximum cross-correlation method to retrieve horizontal current vectors. Singular value decomposition was then applied to isolate the dominant eddy structure from the current field. Finally, a Burgers–Rott vortex model combined with a Levenberg–Marquardt optimization algorithm was used to invert the eddy’s key dynamical parameters, enabling quantitative analysis of its evolution.

The proposed approach opens new opportunities for monitoring ocean dynamics in polar environments using satellite observations. As high-resolution SAR datasets continue to expand, researchers will be able to track multiple eddies simultaneously and analyze their interactions with sea ice, ocean currents, and atmospheric forcing. Such insights could improve numerical models of Arctic circulation and enhance understanding of how polar oceans respond to climate change. In the future, combining satellite observations with oceanographic models and in-situ measurements may provide a more comprehensive picture of Arctic marine processes and their global impacts.

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References

DOI

10.34133/remotesensing.1031

Original Souce URL

https://doi.org/10.34133/remotesensing.1031

Funding information

This work was supported by the National Natural Science Foundation of China (grant number 62231024).

About Journal of Remote Sensing

The Journal of Remote Sensing, an online-only Open Access journal published in association with AIR-CAS, promotes the theory, science, and technology of remote sensing, as well as interdisciplinary research within earth and information science.

Newswise — ATLANTA, March 22, 2026 — Hawaii has a plastic problem. The island state faces economic and logistical challenges in recycling plastic waste, including marine debris that lingers in its ocean waters. Researchers in Hawaii are pioneering a method to recycle the islands’ derelict fishing nets and residential plastic trash into asphalt roads. Early demonstrations show that these recycled materials may provide a viable end-of-life fate for the region’s garbage.

Jeremy Axworthy, a researcher at the Center for Marine Debris Research (CMDR) at Hawaiʻi Pacific University, will present the team’s results at the spring meeting of the American Chemical Society (ACS). ACS Spring 2026 is being held March 22-26; it features nearly 11,000 presentations on a range of science topics.

“This work investigates whether it’s responsible to use recycled plastics in Hawaii’s roads,” shares Axworthy. “By reusing plastic waste that is already in Hawaii, we can reduce the environmental and economic impacts of transporting waste plastics from the islands, incinerating it or dumping it in Hawaii’s overflowing landfills.”

Since 2020, Hawaii’s roads have predominantly been paved with polymer-modified asphalt (PMA) to increase pavement strength and durability. Compared to standard asphalt pavement, PMA pavement is more elastic and more resistant to cracking, rutting and water damage — qualities that are especially important for the state’s tropical climate. PMA pavement is made by first melting pellets of styrene-butadiene-styrene (SBS; a type of copolymer) into a sticky, petroleum-based asphalt binder. Then, the PMA binder is tumbled with heated aggregates (rocks and sand) in a mixing drum, causing the PMA binder to fully coat the aggregates.

But why not see if discarded plastics could be incorporated into asphalt pavements as an environmentally friendly disposal option? How would modified pavements made with recycled plastics perform, and would they release microplastics or associated chemicals into the environment? These are the questions the Hawaii Department of Transportation (HDOT) aimed to answer when they reached out to environmental chemist Jennifer Lynch, CMDR director and team lead.

HDOT asked Lynch’s team for two things. The first was to provide derelict fishing nets removed from Hawaii’s marine environment for the creation of recycled plastic-modified asphalt pavements. “Foreign plastic derelict fishing gear is the largest contributor of Hawaii’s marine debris problem,” shares Lynch. “To date, CMDR’s Bounty Project, which pays a financial reward to licensed commercial fishers for marine debris removal, has removed 84 tons of large, derelict fishing gear from the Pacific Ocean.”

HDOT’s second request was to measure possible microplastic shedding from pavements made with plastic waste versus that from standard SBS-modified pavement. “CMDR’s laboratory is equipped with state-of-the-art chemical instrumentation for quantifying and characterizing microplastics in environmental samples,” explains Lynch. “This capability is incredibly unique and impactful, especially when coupled to our marine debris-removal project and our mission to recycle the debris into long-term, locally necessary infrastructure products.”

Once a U.S.-based company converted the waste into products that could be incorporated into asphalt, HDOT took the experimental asphalt mixes to Hawaii’s streets. A local paving company laid down sections of a residential road on the island of Oahu with asphalt pavement containing standard SBS, repurposed polyethylene from Honolulu’s recycling containers and polyethylene from fishing nets. After about 11 months of regular traffic usage, Lynch’s team stepped in to collect road dust samples from each section of pavement to test for microplastic shedding, which could contaminate the surrounding soil.

The researchers processed the road dust using a method that separates different types of polymers from other materials in the dust, including microplastics, larger chunks of plastic and tire rubber. Using pyrolysis gas chromatography-mass spectrometry (Py-GC-MS), they identified and measured the source of the polymers: styrene and butadiene from the standard PMA, polyethylene from the plastic-waste and fishing-net PMA, and isoprene and butadiene rubber from tires.

Initial tests showed that pavements made with recycled polyethylene did not release more polymers than the control pavement made with SBS. Lynch’s team showed this was true during mechanical performance tests with pavement samples as well as in simulated stormwater collected from the experimental road sections. Microplastic-sized particles were detected, but very few of these were identified as polyethylene regardless of the pavement type tested. This is likely because the polymers are melted into the asphalt binder, meaning particles that break off are not plastic alone; they are a mixture of rock, binder and melted polymer chains.

The CMDR team is also comparing the amount of polymers shed from the pavement to the amount of polymers shed by tires in the road dust. “In our initial Py-GC-MS data,” continues Lynch, “we saw tire wear swamps the signal of polyethylene by orders of magnitude, like gigantic peaks! We had to search the weeds of the chromatogram to find signs of polyethylene.”

Additional research is needed to assess pavement durability. But the researchers are hopeful that someday, repurposing used plastics into pavement could help reduce landfill and marine debris in Hawaii.

“Some people think plastic recycling is a hoax — that it doesn’t work; it’s too challenging,” Lynch shares. “But this work demonstrates that recycling can work when society prioritizes sustainability.”

The research was funded by the Hawaii Department of Transportation.

Visit the ACS Spring 2026 program to learn more about this presentation, “Harvesting ocean plastics to pave hawaiian roads: Evaluation of microplastic and plastic additive release from asphalt incorporating recycled plastic from various waste streams,” and other science presentations.

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Title
Harvesting ocean plastics to pave hawaiian roads: Evaluation of microplastic and plastic additive release from asphalt incorporating recycled plastic from various waste streams

Abstract
Polymer modified asphalt (PMA) is used to increase strength and durability of roads. In Hawaii, PMA is typically produced using the virgin co-polymer styrene-butadiene-styrene (SBS). Recycled plastics, such as high-density polyethylene (HDPE), may also be added to asphalt serving to sequester plastic waste. In the state of Hawaii, derelict fishing gear (DFG) is a significant problem, yet it is also a source of HDPE that can be used in recycling. However, asphalt performance and the consequences of adding recycled polymers to asphalt are not well understood. In collaboration with the Hawaii Department of Transportation (HDOT) and the University of Hawaii (UH), the Center for Marine Debris Research (CMDR) are testing the feasibility of using recycled HDPE in asphalt by quantifying microplastics and plastic additives release from roads paved with asphalts made from different combinations of virgin and recycled polymers. The specific asphalt combinations being tested are: SBS (Control-PMA), DFG with and without SBS (DFG-PMA and DFG-neat), Local Waste recycled HDPE with and without SBS (LW-PMA and LW-neat), and Commercially Available, post-industrial recycled HDPE with and without SBS (CA-PMA and CA-neat). Microplastic and plastic additive release under laboratory conditions were performed using a Hamburg Wheel Tracker Test (HWTT) with water sample analyses. Field trials were conducted on a residential road on the island of Oahu, Hawaii. Road dust was swept and analyzed for microplastics by direct analysis and solvent extraction to separate bound plastic from asphalt and plastic additives by water extraction. Microplastic samples utilized pyrolysis gas chromatography mass spectrometry for analysis. Plastic additives are subjected to solid phase extraction with analysis by gas chromatography mass spectrometry. Results produced using these novel analytical methods provide guidance on the use of recycled plastics over virgin plastics in roadways. Moreover, results of this study may provide a viable end of life fate for plastic marine debris, leading to cleaner and healthier oceans.