When a tunnel catches fire, temperatures inside the concrete lining can soar to 800 or 900 degrees Celsius, and the emergency response almost always involves dousing the structure with water. A new study suggests that this familiar firefighting image—flames followed by a torrent of cooling water—may be doing far more damage to the concrete than engineers have typically accounted for. Researchers investigating basalt fiber-reinforced concrete have found that how a fire-damaged structure is cooled can be as important as how hot it got in the first place, with water quenching consistently inflicting greater strength loss than slow, natural cooling across every temperature they tested.

The research, published in Case Studies in Construction Materials, systematically examined how heating temperature, cooling regime, fiber content, and impact loading combine to determine whether concrete survives a fire with its load-bearing capacity intact. The team, led by Yang Liu and colleagues including Delin Li, Jinyue Dong, Yingda Zhang, Xianliang Zhou, and Qiong Zhou, chose basalt fiber-reinforced concrete, or BFRC, as their test material because of the fiber’s unusual combination of properties. Basalt fibers, drawn from volcanic rock, offer high tensile strength, thermal stability up to melting points between 1350 and 1450 degrees Celsius, and a cost profile far more attractive than premium alternatives such as carbon fiber. This makes them an appealing candidate for tunnel linings, where fire resistance and economy must be balanced.

The experimental design was exhaustive. The researchers prepared a C35-grade concrete mix—the grade commonly recommended for tunnel design—using ordinary Portland cement, medium sand, and continuously graded gravel between 5 and 10 millimeters. Into this base mix they incorporated chopped basalt fibers, 12 millimeters long with a monofilament diameter of 17 micrometers, at volume fractions of 0, 0.1, and 0.2 percent. The fibers were added in small batches during dry mixing to prevent agglomeration, and the fresh concrete was cast into cylindrical specimens measuring 50 millimeters in diameter and 25 millimeters in height, then cured under standard conditions at 20 degrees Celsius and 95 percent relative humidity.

The thermal assault began in a high-temperature electric oven capable of reaching 1200 degrees Celsius. Specimens were heated at a controlled rate of 5 degrees Celsius per minute to target temperatures of 200, 400, 600, and 800 degrees Celsius, then held at temperature for a full hour to ensure the heat penetrated the interior. Half the specimens were then removed and allowed to cool naturally in ambient air, mimicking a structure left to cool on its own after a fire. The other half were plunged immediately into a tank of tap water, replicating the thermal shock of firefighting operations. After cooling, the water-immersed specimens were conditioned in air for seven days to return them to a natural moisture state before testing.

The dynamic mechanical properties were then probed using a split Hopkinson pressure bar, the workhorse instrument for measuring how materials behave under the extreme strain rates produced by impacts and blasts. The apparatus used bars 75 millimeters in diameter, made of high-strength steel with an elastic modulus of 210 gigapascals, with a striker bar propelled by compressed gas striking an incident bar that transmitted stress waves through the specimen. Three impact velocities—3.5, 4.4, and 5.2 meters per second—were tested, achieved by varying the operating gas pressure, with three specimens per condition. A thin pulse shaper was pasted at the impact end of the incident bar to smooth out high-frequency oscillations, and stress equilibrium between the two faces of each specimen was verified from strain-gauge signals, confirming the reliability of the data. Fragments from each impact were sieved through meshes ranging from 4.75 millimeters down to 75 micrometers so that a fractal dimension could be calculated, providing a quantitative measure of how thoroughly each specimen shattered.

The visual evidence of thermal damage followed a familiar but telling progression. At 200 degrees Celsius, the concrete surfaces turned bluish-gray, with no cracking. By 400 degrees, the color shifted to yellowish-gray, still structurally sound. At 600 degrees, fine cracks appeared along with slight surface peeling, and by 800 degrees the specimens showed severe cracking, spalling, and edge breakage. Water-cooled specimens generally exhibited more pronounced surface damage than their naturally cooled counterparts, and at 800 degrees the concave shape at the start of the stress-strain curve—evidence of pre-existing microcracks being closed under compression—was especially marked in the water-quenched samples.

The strength data told a stark quantitative story. For naturally cooled specimens containing 0.2 percent basalt fiber, the dynamic peak stress at an impact velocity of 3.5 meters per second fell from 51.1 megapascals at room temperature to 18.6 megapascals at 800 degrees—a reduction of 63.6 percent. Water cooling made matters worse across the board: at the same impact velocity, the reductions reached 23.9 percent at just 200 degrees and climbed to 64.9 percent at 800 degrees. Averaged across the temperature range, each 100-degree increment cost naturally cooled specimens roughly 6.7 to 8.0 percent of their strength, while water-cooled specimens lost about 7.5 to 8.1 percent per 100 degrees. The gap between the two cooling regimes widened at higher impact velocities: at 5.2 meters per second and 800 degrees, the water-cooled specimens suffered 6.4 percent greater strength loss than the naturally cooled ones, whereas at the lowest velocity the difference was a mere 1.3 percent. The explanation lies in competing timescales—at slow loading rates, cracks have time to propagate and dissipate energy, blunting the effect of water-induced damage, but at high rates the loading outpaces the material’s energy dissipation, and the microcracks created by thermal shock propagate catastrophically.

Against this backdrop of degradation, the basalt fibers demonstrated genuine protective power. At every temperature from 200 to 800 degrees, specimens with 0.2 percent fiber content outperformed both plain concrete and the 0.1 percent mix. At 400 degrees and an impact velocity of 3.5 meters per second, the naturally cooled fiber-reinforced specimens reached peak stresses of 40.1 megapascals, some 16.9 percent above plain concrete, while at 200 degrees under water cooling the 0.2 percent mix achieved 38.8 megapascals—a remarkable 32.4 percent improvement over unreinforced concrete. The mechanism, the authors explain, is architectural: randomly distributed fibers form a three-dimensional network that binds tightly with the cementitious matrix, reduces internal pores and cracks, and bridges microcracks before they can coalesce into fracture surfaces. But this protection has a ceiling. Above roughly 600 degrees, the fibers begin to degrade and lose their reinforcing capability, and the fiber-matrix interface—already weakened by thermal mismatch between fiber and paste—becomes a liability during water quenching.

Fractal analysis of the impact debris added another layer of insight. The fractal dimension of the fragments rose steadily with temperature, from around 1.82 at 200 degrees to above 2.3 at 800 degrees under the highest loading rate, indicating progressively finer and more complex fragmentation. Water-cooled specimens consistently shattered into finer pieces than naturally cooled ones, particularly at 600 and 800 degrees, confirming that the steep thermal gradients during quenching seed dense populations of microcracks that later explode into fracture networks under impact.

Microstructural investigation grounded these observations in chemistry and physics. X-ray diffraction of specimens heated to 800 degrees showed the disappearance of calcium hydroxide peaks and weakened calcium carbonate signals, evidence that these phases had thermally decomposed—reactions that release vapor, increase porosity, and weaken the matrix. Scanning electron microscopy revealed the deterioration in vivid detail: an unheated specimen showed a dense microstructure with abundant calcium-silicate-hydrate gel and a compact interfacial transition zone around each aggregate, while specimens heated to 800 degrees contained no detectable C-S-H gel at all, their structure riddled with pores and cracks and hosting instead a dicalcium silicate-like phase. Comparing cooling regimes at 400 degrees, the naturally cooled sample remained relatively dense and rich in hydration products, whereas its water-quenched twin displayed obvious cracks at the interfacial transition zone and a loosened surrounding matrix—the fingerprint of thermal shock stress racing through the cooling material.

The practical implications reach well beyond the laboratory. Tunnel linings that survive a fire are routinely assessed and, if necessary, repaired, but this study shows that the assessment itself must account for the cooling history. A lining quenched by firefighting water may be significantly weaker than its peak temperature alone would suggest, particularly if it subsequently faces dynamic loads from traffic vibration, rockfall impacts, or secondary events. Conversely, the results give engineers a positive tool: specifying basalt fiber reinforcement at around 0.2 percent by volume can meaningfully bolster the impact resistance of fire-exposed concrete below 600 degrees, at a modest material cost. The authors frame their work as a theoretical foundation for post-fire safety assessment of tunnel linings and for the wider engineering adoption of basalt fiber-reinforced concrete—a reminder that in structural fire engineering, what happens in the minutes after the flames matter almost as much as the fire itself.

Scientists have unveiled a computational design for a terahertz metasurface biosensor that combines five distinct materials—graphene, MXene, tungsten disulfide, gold, and copper—into a single multilayer architecture capable of detecting refractive-index changes associated with chikungunya virus infection. The study, published in Results in Optics by G. Arunachalam, A.R. Kalaiarasi, Giri.G. Hallur, and V. Parthasarathy, reports a numerically predicted sensitivity of 907 GHz per refractive-index unit, among the highest values reported for hybrid-material terahertz biosensors, and couples the electromagnetic design to an XGBoost machine-learning surrogate model that predicts sensor behavior with accuracies exceeding 99.8 percent.

Chikungunya virus is an enveloped, positive-sense single-stranded RNA alphavirus transmitted primarily by Aedes aegypti and Aedes albopictus mosquitoes. While mortality remains low, generally below 0.1 percent, the broader public health burden arises from severe polyarthralgia that can persist for months or even years in a substantial fraction of patients across tropical and subtropical regions. With no approved antiviral therapy or licensed vaccine currently available, diagnostic accuracy sits at the center of clinical management and transmission control. Yet existing diagnostic tools face significant practical constraints, particularly in point-of-care and field settings.

Serological methods such as enzyme-linked immunosorbent assay suffer from cross-reactivity with related alphaviruses, including Ross River and O’nyong-nyong viruses, reducing diagnostic specificity. Real-time reverse transcription polymerase chain reaction offers high sensitivity during the acute phase but depends on laboratory infrastructure, trained personnel, and controlled sample handling. Virus isolation in cell culture provides confirmatory results but requires biosafety level-3 facilities and extended processing time. These limitations have motivated the search for rapid, label-free sensing approaches capable of operating at clinically relevant concentrations in decentralized environments.

The new work turns to the terahertz band, spanning roughly 0.1 to 10 THz, which lies between microwave and infrared regions of the electromagnetic spectrum. Terahertz radiation is non-ionising, with photon energies in the millielectronvolt range, allowing interaction with biological samples without causing ionising damage. Crucially, terahertz waves couple to low-frequency vibrational and rotational modes of biomolecules such as proteins, nucleic acids, and polysaccharides, producing measurable spectral features that support label-free detection. Because biological media including blood plasma and viral suspensions exhibit refractive-index variations in this domain, differences on the order of 0.01 to 0.02 refractive-index units can shift resonance frequency and field distribution when coupled to resonant sensing structures.

The proposed sensor is built around a periodically repeated square unit cell containing two identical square resonators, 2000 nanometers on a side, coated with tungsten disulfide—a two-dimensional transition metal dichalcogenide with strong light–matter interaction, high carrier mobility, and excellent dielectric confinement. This layer localizes the electric field in the sensing region and increases the interaction volume between the resonant field and the surrounding analyte. A pair of concentric circular rings, 3200 and 3800 nanometers in diameter and functionalized with MXene, surrounds the resonators, enhancing electromagnetic coupling, promoting efficient charge transport, and strengthening plasmonic interactions between resonator elements. An outer gold ring, 6000 nanometers in diameter, serves as the main plasmonic resonator supporting strong localized surface plasmon resonances with low optical loss. The entire multi-resonant assembly is embedded within a monolayer graphene sheet measuring 14,000 by 14,000 nanometers, which acts as a broadband absorber and a high-mobility charge transport medium whose electrically tunable chemical potential allows dynamic, active control of the resonance characteristics. Copper elements woven into the architecture provide supplementary conductive pathways that reinforce current distribution and coupling among the hybrid resonators. The structure rests on a silicon dioxide substrate, chosen for its low dielectric loss and mechanical robustness, which preserves the resonance quality factor.

The authors stress that the multilayer design is compatible with established microfabrication techniques. Fabrication would begin with a cleaned silicon dioxide substrate, followed by polymer-assisted transfer of monolayer graphene and thermal annealing. Gold and copper resonators can be deposited through electron-beam evaporation or magnetron sputtering with lift-off patterning, MXene rings through solution-based deposition, and the tungsten disulfide layer through chemical vapor deposition or thin-film transfer. With a unit-cell dimension of approximately 14 micrometers, the required feature sizes fall comfortably within conventional photolithography capabilities, and because fabrication imperfections remain far smaller than the operating terahertz wavelength, moderate tolerances are expected to have only limited influence on the electromagnetic response. For biosensing, the graphene surface could subsequently be functionalized with chikungunya-specific antibodies or aptamers using EDC/NHS or pyrene-based linker chemistries.

The electromagnetic modeling, performed in COMSOL Multiphysics, reveals a pronounced resonance at 0.355 THz, where electric-field simulations show the strongest and most spatially extensive enhancement. Varying the graphene chemical potential from 0.1 to 0.9 electronvolts produced dramatic modulation of the transmission contrast, which increased roughly 36-fold at the highest bias, from less than one percentage point to more than 27 percentage points, while peak transmission remained essentially unchanged above 98.6 percent. This asymmetric response—stable maxima paired with strongly modulated minima—arises because increasing chemical potential enhances graphene’s intraband conductivity, deepening resonant absorption through stronger light–matter interaction. The sensor also demonstrated remarkable angular robustness, maintaining peak transmittance above 97.8 percent across incident angles from 0 to 80 degrees, an important tolerance for realistic deployment where normal incidence cannot always be guaranteed.

Geometric optimization identified an outer circular resonator radius of 2500 nanometers and a square resonator side length of 2500 nanometers as the dimensions that maximize resonance strength, driving minimum transmittance down to approximately 65 to 67 percent and signifying optimal electromagnetic confinement within the active sensing region. When evaluated across refractive indices from 1.33 to 1.39, a range encompassing reported values for healthy plasma (approximately 1.35 RIU), healthy platelets (1.39 RIU), chikungunya-infected plasma (1.33 RIU), and infected platelets (1.38 RIU), the optimized configuration achieved a maximum sensitivity of 907 GHz/RIU, a figure of merit of 18.519 RIU⁻¹, a minimum detection limit of 0.061 RIU, a sensor resolution of 55.178, and a refractive-index resolution of 0.001 RIU. In comparative benchmarks against recently reported graphene- and hybrid-material-based terahertz biosensors—including graphene/copper/aluminum, graphene/silicon dioxide, MXene–graphene–black phosphorus, and graphene-integrated copper–silver designs—the proposed architecture’s sensitivity exceeded most published values, reflecting the synergistic field confinement produced by the five-material stack.

The machine-learning component addresses one of the central bottlenecks in metasurface development: the computational cost of repeated full-wave finite-element simulations during structural optimization. The team trained an XGBoost regressor, an ensemble method based on gradient-boosted decision trees, on simulation data covering incidence-angle variation and circular-ring dimension variation, using stratified sampling with 80 percent of data for training and 20 percent held out for independent testing, alongside five-fold cross-validation and grid-search hyperparameter optimization. The model captured more than 99.7 percent of response variance on unseen data, with mean absolute percentage errors below 0.162 percent and prediction accuracies from 99.838 to 99.959 percent. Acting as a computational surrogate, the trained model enables rapid interpolation across the design space without sacrificing the fidelity of the underlying electromagnetic model.

The authors are careful to frame the work as a computational proof-of-concept rather than an experimentally validated diagnostic. The sensor detects changes in the local dielectric environment surrounding the resonators, not viral particles or nucleic acids directly, and refractive-index sensing alone cannot intrinsically distinguish chikungunya from other viruses with similar dielectric properties. Analytical specificity in practice will depend on surface biofunctionalization with chikungunya-specific recognition molecules immobilized on the graphene or gold sensing surface. Future work will focus on device fabrication, biofunctionalization, calibration with reference refractive-index standards, experimental validation with clinically relevant plasma and platelet samples, and systematic evaluation of selectivity against related arboviruses—steps that would transform this numerically validated platform into a practical tool for rapid, label-free infectious disease diagnostics in the field.

The ocean has quietly absorbed billions of tons of humanity’s carbon emissions over the past two centuries, but scientists and companies racing to supercharge that natural service have long been hampered by a stubborn and costly engineering problem. Now researchers at Stony Brook University, working with the Research Foundation for the State University of New York, have unveiled a method for electrochemical ocean alkalinity enhancement that they say can dramatically lower the cost of ocean-based carbon dioxide removal by eliminating one of the most expensive steps in the entire process: the pretreatment of seawater before it enters an electrochemical reactor. The innovation, now available for licensing through SUNY TechConnect, promises high-quality carbon offsets at a substantially reduced cost while simultaneously helping to counteract the acidification that threatens marine ecosystems worldwide.

At the heart of the challenge is a delicate chemical balancing act. As atmospheric carbon dioxide dissolves into seawater, it forms carbonic acid, which lowers the ocean’s pH and erodes the carbonate chemistry that corals, shellfish and other calcifying organisms depend upon. Ocean carbon dioxide capture exploits a simple principle: if the ocean becomes more alkaline, it can absorb more CO2 from the air and lock it away safely as bicarbonate, one of the most stable and abundant forms of inorganic carbon on Earth. This process, known as ocean alkalinity enhancement, effectively turns the surface ocean into a vast, distributed carbon sink. But adding alkalinity to seawater is not trivial, and doing it in a way that is energy-efficient, scalable and safe has become one of the central engineering puzzles of the emerging carbon removal industry.

One of the most promising approaches relies on electrochemistry, specifically a technique called bipolar membrane electrodialysis. In this system, ion-selective membranes are stacked between two end electrodes, and the arrangement allows operators to split ordinary saltwater into its constituent acid and base. When brine containing sodium chloride flows through the stack, the process generates hydrochloric acid on one side and sodium hydroxide, a strong base, on the other. The elegance of the scheme lies in its product handling: if the hydrochloric acid is kept on land, where it can be stored, neutralized or put to industrial use, and only the sodium hydroxide along with the treated seawater is returned to the ocean, the receiving waters gain a net infusion of alkalinity. That added alkalinity shifts the carbonate equilibrium, allowing the ocean to draw down carbon dioxide from the atmosphere and convert it into dissolved bicarbonate that remains stable for millennia.

This electrochemical pathway has attracted serious commercial interest precisely because it produces what carbon markets call negative emissions, meaning carbon dioxide is durably removed from the atmosphere rather than merely avoided. Companies pursuing net-zero targets increasingly rely on such carbon removal credits to offset their residual emissions, and ocean alkalinity enhancement is widely regarded as one of the largest-capacity avenues available, given the sheer scale of the world’s oceans. Yet the technology has been held back by a deceptively mundane problem: what flows into the reactor matters just as much as what flows out.

Seawater, and many other brine streams that might feed these systems, contains divalent cations, most notably calcium and magnesium ions, alongside the sodium and chloride that the process is designed to split. When these divalent ions encounter the high-pH conditions created at the base-producing side of a bipolar membrane stack, they precipitate as solid calcium and magnesium compounds that coat the membranes in a crust known as scale. The consequences are cascading. Scaled membranes lose their ion-selective efficiency, forcing the system to push harder and consume more electricity to achieve the same output. Over time, the deposits shorten membrane lifetime, increasing maintenance frequency and replacement costs. The conventional answer has been water softening pretreatment, in which the incoming seawater is stripped of calcium and magnesium before it ever reaches the electrodialysis unit. While effective, such pretreatment adds significant capital and operating expense, undermining the economic case for the entire carbon removal operation and eroding the value proposition of the resulting carbon credits.

The Stony Brook researchers behind the new method have essentially designed around this bottleneck. Their technology enables electrochemical enhancement of ocean alkalinity without any pretreatment of the incoming seawater at all. By rethinking how the electrochemical system handles brine streams laden with divalent cations, the researchers have created a process that tolerates raw seawater directly, sidestepping the water softening infrastructure that previous designs demanded. According to the announcement from the Research Foundation for SUNY, the result is a system that produces negative emission carbon offsets of very high quality at a substantially reduced cost, simply because the most expensive upstream step has been engineered out of existence. The advantages claimed for the approach are straightforward and commercially significant: it is cheaper, more energy efficient, and requires no expensive water softening pretreatment.

The implications ripple across both the carbon markets and the broader climate technology landscape. Carbon offset buyers, including corporations striving to meet net-zero commitments, place a premium on removal credits that are durable, verifiable and cost-competitive. Ocean alkalinity enhancement already offers exceptional permanence, since bicarbonate dissolved in seawater represents one of the most long-lived forms of carbon storage known. By cutting costs at the front end, the Stony Brook method could help push the price of these high-quality ocean-based offsets toward levels that make them viable at gigatonne scale, a threshold that analysts consider essential if carbon removal is to play a meaningful role in stabilizing the global climate. Cheaper alkalinity generation also strengthens the second major application of the technology: mitigating ocean acidification directly, without necessarily framing it as a carbon market product at all.

Ocean acidification itself is a mounting crisis. Since the industrial revolution, the average surface ocean pH has dropped measurably as the sea has absorbed roughly a quarter to a third of anthropogenic CO2 emissions. The consequences have been documented across coral reefs, oyster hatcheries, pteropods and other calcifying organisms whose shells and skeletons become harder to build in increasingly acidic waters. A technology that adds alkalinity to coastal waters and open ocean regions simultaneously addresses this chemical stress and harvests the carbon removal benefit, a dual function that distinguishes ocean alkalinity enhancement from many other carbon removal approaches. In regions where fisheries, aquaculture and reef ecosystems are economically vital, localized deployment of alkalinity-enhancing electrochemical systems could offer both environmental resilience and revenue through carbon credit sales.

The scientific pedigree of the work reflects the growing maturity of the carbon removal field. Stony Brook University, a flagship research institution within the SUNY system, has become an active hub for climate and energy innovation, and the new method is protected under intellectual property identified in the licensing announcement. The Research Foundation for the State University of New York, the nation’s largest research foundation supporting the nation’s largest public university system, is actively seeking development partners, commercial partners and licensees to translate the laboratory advance into deployed systems. The foundation describes a broad portfolio of SUNY-led research spanning artificial intelligence for the public good, quantum technologies, next-generation semiconductors, biotechnology and medicine, and energy and climate solutions, with system-wide research expenditures approaching 1.5 billion dollars in fiscal year 2025.

For the carbon removal industry, the timing of the announcement is notable. As voluntary and compliance carbon markets mature, buyers are demanding higher fidelity in the offsets they purchase, favoring durable removal over avoidance-based credits. Electrochemical ocean alkalinity enhancement, with its well-understood chemistry and measurable inputs and outputs, is well positioned to meet rigorous monitoring, reporting and verification standards. The obstacle has always been cost, and the pretreatment bottleneck has been a substantial contributor. If the Stony Brook design performs as described at industrial scale, it could remove one of the largest cost wedges standing between laboratory demonstration and commercial deployment, accelerating a technology class that many climate analysts view as indispensable to achieving deep decarbonization.

The broader lesson of the advance may be as important as the technology itself. In the race to scale carbon removal, progress often comes not from exotic new chemistry but from eliminating the hidden costs and fragilities that make promising concepts uneconomic in practice. Water softening pretreatment is exactly the kind of unglamorous engineering detail that determines whether a climate technology remains a paper exercise or becomes infrastructure. By designing a bipolar membrane electrodialysis system that thrives on untreated seawater, the Stony Brook researchers have addressed one of those decisive details. The ocean, meanwhile, stands ready. Every unit of alkalinity added is an invitation for the sea to take up more carbon dioxide and, in doing so, to heal a little of the acidification that a warming world has inflicted upon it. What remains now is the work of scaling, partnering and commercializing, and the SUNY licensing announcement signals that the researchers and their institution intend to see this chemistry leave the laboratory and reach the sea.

Artificial intelligence (AI) combined with virtual reality (VR) could guide us through tomorrow's cities before they are even built, according to research in the International Journal of Environment and Pollution. Such models could be useful for architects, planners and policymakers.

Researchers from the European AM2SoftMag project have developed a new iron-based metallic glass that could lead to 3D-printed components for the manufacture of more efficient electric motors. The new alloy, designed by researchers at Saarland University (UdS) in Germany, is free of critical elements with significant social impacts, such as cobalt, and elements with unstable supply chains, such as rare earths. In addition, it can be 3D printed in a fully amorphous state and with a density exceeding 92%, giving it exceptional magnetic properties.

Researchers at AIST, in collaboration with researchers at the National Institute of Technology, Kagoshima College, have developed the Anaerobic Baffled Continuous Stirring (ABCS) reactor, a device capable of simultaneously treating solid waste and wastewater from biomanufacturing processes while recovering methane for energy self-sufficiency.

In order to survive, the first humans to reach Mars will immediately need a safe and reliable place to set up shop. But building on Earth’s neighbor is immensely more challenging than construction projects at home. The Martian surface is a practically airless vacuum, constantly bombarded with radiation, and regularly reaches temperatures as low as -81 degrees Fahrenheit.

However, there is a very specific process on Earth that approximates similar conditions to the Red Planet: freeze-drying. According to researchers at The Hong Kong University of Science and Technology, the same method used to preserve perishable foods could also inspire sturdy and even recyclable 3D-printed houses on Mars. The secret ingredients? Everyday gelatin and yeast. The novel approach is detailed in a study published today in the journal Chem Circularity.

“My inspiration came from freeze-dried fruits that become harder. So I asked myself if we can take advantage of that and make some materials,” Jishen Qiu, a study co-author and civil engineer, said in a statement.

The combination of materials are simple: sand and an adhesive binder. Since gluing tiny rocks together requires specialized stickiness, Qiu’s team invented a new concoction from gelatin and lab engineered yeast. When mixed, the yeast microbes become coated with adhesive proteins similar to those used by mussels to anchor on stones underwater. The goop is then extruded through a 3D printer nozzle into an extremely cold, low-pressure environment, where it solidifies as the water instantly freezes and converts from ice to vapor. The final result is a light, porous, foam-like material that remains very resilient.

“This is actually strong enough to build a one- or two-story building on Earth—whose gravity is three times that of Mars,” explained Qiu. “So, you can probably easily build a multistory building on Mars with the material.”

Qiu and his collaborators know they must first start small before expanding to Martian neighborhoods. Their prototype domes are only about the size of a wine cork at this point, but their compressive strength is comparable to low-grade concrete.

Engineers have experimented with 3D-printed structures to use on the moon and Mars for years, but many of these still require steps like melting down rocks or lunar regolith. These methods usually require a lot of extra energy, which may limit their utility. Qiu’s technique requires comparatively little energy, although he admits it’s still unclear if yeasts can withstand life on Mars. That said, the team’s early results are a promising step towards simple, efficient, and sturdy buildings beyond Earth. If nothing else, yeast also lends itself to trial-and-error.

“As long as there’s one yeast that’s still alive, you can grow them again,” added Qiu.

The post Mars astronauts could live in houses 3D-printed from freeze-dried yeast appeared first on Popular Science.

Signals that appear to show ions moving through a battery material may sometimes be caused by nothing more than a rough surface, according to new research from the Korea Advanced Institute of Science and Technology, or KAIST. The discovery could help scientists avoid misleading measurements while developing faster-charging and longer-lasting batteries. It may be especially […]

The post Scientists Discover Hidden Flaw in Nanoscale Battery Testing appeared first on Knowridge Science Report.

Drilling for electricity or geothermal energy is a common human-caused source of earthquakes. Drillers or engineers inject water into the earth to fracture underground rock through a process known as fracking. This allows scientists to produce clean energy almost anywhere on Earth by heating up water in the cracks using facilities called enhanced geothermal systems or EGS plants. However, fracking causes earthquakes, which are a major concern for people’s safety globally. Therefore, scientists are looking for new fracking methods that cause fewer earthquakes.

Fracking for EGS plants can trigger earthquakes by changing the pressure underground and adding stress to the surrounding rock. However, these earthquakes happen at pre-existing, naturally occurring cracks called faults, which are different from the newly formed, man-made cracks. Faults are naturally under pressure from the overlying rock and the surrounding earth since they reach deep underground. As pressure builds up over time, it eventually causes the rocks to shift along these faults and release energy in the form of earthquakes. 

During fracking, engineers use 4 different shut-in strategies to finish off water pumping. The standard industry strategy is called instant shut-in, where the injection pump is turned off immediately, but the water stays underground, causing the pressure to lower naturally. In a similar strategy, known as the tapered shut-in, engineers gradually reduce the water injection rate to zero instead of immediately turning it off. For the high-rate and low-rate extraction strategies, they pump the water back out after injection is complete, at different pump rates.

Recently, scientists aimed to mitigate the risk of earthquakes by testing these 4 shut-in strategies to determine which is most effective. They compared the shut-in strategies using crystalline basement rock with low porosity and permeability, meaning water couldn’t easily flow through it. Engineers use this same type of rock for EGS plants so they can control where the water flows. The scientists pumped water into the rock, then measured the pressure and stress levels where rocks began to move along faults, determining the point at which earthquakes would occur. 

The scientists applied high-rate and low-rate extraction methods to the rock and found that pressure and fault movements decreased. However, when they applied instant and tapered shut-in methods to the same rock, they increased the pressure and caused continuous fault slipping. They measured stress in the rock during these methods and found that high-rate extraction stabilized the fastest, while low-rate extraction stabilized more slowly. In contrast, instant shut-in continuously increased the pressure and slip, and tapered shut-in caused the highest stress of all.

The scientists also used a computer model to simulate what happened at an EGS site in South Korea, where earthquakes occurred after injections using the instant shut-in method. They set up the model using a rock with the same characteristics, injection wells, and faults as that site. Then, they simulated periods of injection based on the previous real-world events and modeled the effects of pressure and stress to determine if the earthquakes could have been prevented. 

The team used the model to compare how a site like this would respond to the instant shut-in method versus the other shut-in methods. They found that the tapered shut-in method increased pressure and stress in the rock, while the high-rate and low-rate methods both decreased pressure and stress. The high-rate method decreased pressure and stress more than the low-rate method. 

The scientists concluded that high-rate extraction is the most effective method for reducing the risks of post-injection earthquakes during EGS fracking in crystalline basement rock. Additionally, the scientists determined that the earthquakes in South Korea could have been prevented if engineers had used either the high-rate or low-rate extraction methods. They recommend using high-rate extraction to reduce earthquakes during EGS fracking, which would allow EGS plants to generate clean energy more safely.

The post Reducing earthquakes caused by fracking appeared first on Sciworthy.

Além de servir como uma rede social com conteúdos para passar o tempo, o TikTok também possui um grande número de criadores de conteúdo focados em publicações de cunho educacional.

Para incentivar e expandir o acesso a esses posts, a rede social permite ativar o chamado Feed STEM (Science, Technology, Engineering and Mathematics, ou Ciência, Tecnologia, Engenharia e Matemática).

Apesar de já vir ativado para usuários entre 13 e 17 anos, todos podem ativar o filtro STEM manualmente. Veja como! 😄

1. Com o app do TikTok aberto, toque na aba “Perfil”;
2. Toque nos três risquinhos (no canto superior direito);
3. Vá até “Configurações e privacidade”;
4. Escolha “Preferências de conteúdo”;
5. Toque em “Feed STEM”;
6. Selecione “Ativar”.

Volte à tela inicial do TikTok e deslize o dedo da esquerda para a direita (na parte superior) para escolher “STEM”.

Opcionalmente, também é possível ativar as legendas.

The Korea Research Institute of Standards and Science (KRISS) has developed a deep learning technology that predicts, in real time, vibrations at multiple locations inside a nuclear power plant using the signal from just a single seismometer and quantifies the risk at each location to enable the prioritization of inspections. In particular, because the AI model can be flexibly designed to match the vibration characteristics of a structure, it is expected to be widely applicable to major industrial facilities such as semiconductor plants and data centers in the future.

Scientists project that by 2050, nearly half the global urban population will not have enough potable water—a 50% increase since 2016. New and sustainable methods for desalination are needed, and Cornell researchers have one potential solution—in part inspired by the bird of paradise.