Monday, March 30, 2026

Green Chemistry: Ketotifen Detection! #worldresearchawards #Analyticalchemistry #researchawards

 


This study presents a green chemistry-driven quality by design strategy for the sensitive voltammetric determination of ketotifen fumarate using a nano-zirconium oxide modified electrode, enhancing analytical performance, sustainability, selectivity, and reproducibility while minimizing environmental impact and reagent consumption significantly overall.

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Saturday, March 28, 2026

Scientists turn CO2 into fuel using breakthrough single-atom catalyst


Researchers have created a cutting-edge catalyst that turns CO2 into methanol more efficiently than ever before. Instead of using clumps of metal atoms, they engineered a system where each single indium atom actively drives the reaction. This dramatically reduces energy needs while making the process easier to study and optimize. The result could accelerate the shift toward cleaner fuels and sustainable chemical production.



Every chemical reaction must overcome an energy hurdle before it can occur. Substances need an initial input of energy to start reacting. Sometimes this barrier is small, like lighting a match. In many industrial processes, however, the required energy is much higher, which increases costs.

To make reactions easier and more efficient, chemists rely on substances called catalysts. These "reaction helpers" reduce the energy needed. The most effective catalysts often contain metals, including rare and expensive ones.

Breakthrough Catalyst Turns CO2 Into Methanol

Researchers at ETH Zurich have now made a major advance in catalyst design. Their new system significantly lowers the energy needed to produce methanol (an alcohol) from carbon dioxide and hydrogen.

The team also achieved an unusually efficient use of the metal indium. In this catalyst, each individual indium atom acts as its own active site. This is a major shift from traditional approaches, where metals are grouped in particles.

Another key advantage is improved precision. In the past, catalyst development often relied on trial and error. This new design allows scientists to better observe and understand the reactions happening on the surface, opening the door to more deliberate and optimized catalyst development.

Methanol's Role in Sustainable Chemistry

"Methanol is a universal precursor for the production of a wide range of chemicals and materials, such as plastics the Swiss army knife of chemistry, so to speak," says Javier Pérez-Ramírez, Professor of Catalysis Engineering at ETH Zurich.

Methanol is essential for producing fuels and materials, and it plays a growing role in efforts to move away from fossil fuels. If the hydrogen and energy used in the process come from renewable sources, methanol production could become climate neutral.

This approach also offers a new way to use CO2. Instead of releasing it into the atmosphere, it can be captured and turned into a valuable raw material.

Single Atom Catalysts Maximize Efficiency

"Our new catalyst has a single atom architecture, in which isolated active metal atoms are anchored on the surface of a specially developed support material," Pérez-Ramírez explains.

In conventional catalysts, metals are typically grouped into small particles that can contain hundreds or even thousands of atoms. Many of those atoms are not directly involved in the reaction, making the process less efficient.

Single atom catalysts represent a more efficient alternative. By using metals at the level of individual atoms, scientists can make better use of scarce and costly elements. In some cases, this even makes it practical to use precious metals in industrial applications.

Working with isolated atoms can also change how the catalyst behaves. "Indium has already been used in this catalyst for over a decade," says Pérez-Ramírez. "In our study, we show that isolated indium atoms on hafnium oxide allow more efficient CO2-based methanol synthesis than indium in the form of nanoparticles containing large numbers of atoms."

Engineering Stable Single Atom Catalysts

To place individual indium atoms precisely on the surface of hafnium oxide, the ETH team developed several new synthesis methods in collaboration with other research groups. A critical factor was designing a support material that keeps the atoms stable while still allowing them to remain reactive.

One method involves burning the starting materials in a flame at temperatures between 2,000 and 3,000°C, followed by rapid cooling. Under these conditions, indium atoms remain on the surface and become firmly embedded.

The resulting catalyst is highly durable. The researchers showed that these single atom systems can withstand demanding conditions, including high temperatures and pressures. This is important because producing methanol from CO2 and hydrogen typically requires temperatures up to 300°C and pressures up to 50 times normal atmospheric levels.

Clearer Insights Into Reaction Mechanisms

Traditional catalysts made of nanoparticles have long been difficult to study. Although reactions occur at surface atoms, many signals in measurements come from atoms inside the particles that do not participate in the reaction. This makes it harder to interpret what is really happening.

With single atom catalysts, this problem is reduced. Because only isolated atoms are present, scientists can analyze reaction mechanisms with far less interference, leading to clearer insights.

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Friday, March 27, 2026

3D Printing Revolutionizes CO2 Conversion! #worldresearchawards #Analyticalchemistry #researchawards

 


3D printing-enabled fabrication of nitrogen and boron co-doped porous carbon electrodes derived from poly(ionic liquid) offers a scalable strategy for efficient CO₂ electroconversion. The tailored porosity, conductivity, and active sites enhance catalytic performance, selectivity, and sustainability in carbon capture and utilization technologies.

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Thursday, March 26, 2026

Breakthrough Catalyst Turns CO2 Into Fuel With Incredible Efficiency




A redesigned catalyst appears to sidestep a major bottleneck in CO2-to-methanol conversion by separating where key reaction steps occur.

Efficient methanol production could play an important role in carbon recycling, turning captured carbon dioxide (CO2) into a useful chemical feedstock and fuel ingredient. In principle, the chemistry works best at low temperatures, where converting CO2 into methanol is thermodynamically favorable. In practice, though, there is a major obstacle: CO2 is hard to activate under those milder conditions, so catalysts tend to perform poorly.

Turning up the heat helps the reaction move faster, but it creates another problem. Higher temperatures also encourage the reverse water gas shift reaction, which diverts CO2 toward carbon monoxide instead of methanol. That leaves researchers stuck with a familiar trade-off.

Conditions that improve activity often hurt selectivity, and conditions that favor selectivity often reduce output. This balancing act has been a major barrier to boosting methanol yield.

A New Catalyst Design Strategy

In a study published in Chem, a team led by Prof. Jian Sun and Prof. Jiafeng Yu at the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS) introduced a new catalyst design. Their approach separates active sites in space using a strong metal support interaction (SMSI) driven overlayer structure, improving the efficiency of methanol production from CO2.

The team reshaped the catalyst surface and altered how reactants attach and break apart, as well as how the reaction proceeds. Under conditions of 300 ℃ (572 °F) and 3 MPa (about 435 psi), the system reached a space time yield of 1.2 g·gcat-1·h-1. This performance is roughly three times higher than that of standard commercial Cu/Zn/Al catalysts.

How the Reaction Pathway Changes

The researchers discovered that their design directs CO2 to adsorb and activate mainly on zirconia (ZrO2), steering the process toward methanol formation through the formate pathway.

This differs from the usual mechanism on copper sites, where the C=O bond is broken before hydrogenation. In the new system, hydrogenation happens first on ZrO2, followed by cleavage of the C=O bond. This shift reduces the formation of unwanted CO while maintaining the strong ability of copper sites to split H2.

“Our study may provide a new pathway to addressing the long-standing trade-off between activity and selectivity in methanol synthesis from CO2,” said Prof. Sun.

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Molten Slag Magic: Carbon & Syngas! #worldresearchawards #Analyticalchemistry #research

 


This study explores molten slag etching at ultrahigh temperatures to convert carbonaceous materials into porous carbon while upgrading syngas composition. The process enhances surface area, energy efficiency, and valorizes waste streams for sustainable industrial applications with reaction kinetics and selectivity.

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Wednesday, March 25, 2026

Scientists Just Built Atom-Sized Gates That Act Like Living Cells



Scientists have built atom-sized pores that act like living ion channels, opening the door to next-generation nanotech.

Ion channels are extremely narrow pathways that are essential for many processes in living systems. To understand how ions move through these confined spaces, scientists need to build artificial pores at incredibly small scales. The tightest parts of these channels can be only a few angstroms wide, roughly the size of single atoms, which makes precise and repeatable fabrication very difficult with current nanotechnology.

Researchers at the University of Osaka have now tackled this problem. In a study published in Nature Communications, they describe a new approach that uses a miniature electrochemical reactor to form pores that approach subnanometer size.

How Ion Channels Generate Electrical Signals

In living cells, ions pass through protein channels embedded in the cell membrane. This flow of ions creates electrical signals, including nerve impulses that control muscle movement. These protein channels contain extremely narrow regions and can switch between open and closed states. External signals trigger changes in the protein structure, which in turn regulate the flow of ions.

A Solid-State System That Mimics Biology

Inspired by these natural mechanisms, the research team created a solid-state system capable of forming pores close in size to biological ion channels. They started by forming a nanopore in a silicon nitride membrane. This nanopore then acted as a tiny reaction chamber where even smaller pores could be generated.

When a negative voltage was applied across the membrane, it triggered a chemical reaction inside the nanopore that produced a solid precipitate. As this material accumulated, it gradually filled and blocked the pore. Reversing the voltage caused the precipitate to dissolve, restoring pathways for ions to pass through.

“We were able to repeat this opening and closing process hundreds of times over several hours,” explains lead author Makusu Tsutsui. “This demonstrates that the reaction scheme is robust and controllable.”

Electrical Spikes and Tunable Ion Transport

The researchers tracked the flow of ions through the membrane and observed sudden spikes in current. Similar patterns are seen in natural ion channels. Their analysis indicates that these signals likely arise from the formation of many subnanometer pores within the original nanopore.

They also found that the system could be adjusted to change how the pores behave. By modifying the composition and pH of the reactant solutions, they were able to control the size and properties of the ultrasmall pores.

“We were able to vary the behavior and effective size of the ultrasmall pores by changing the composition and pH of the reactant solutions,” reports Tomoji Kawai, senior author. “This enabled selective transport of ions of different effective sizes through the membrane by tuning the ultrasmall pore sizes.”

Potential Uses in Sensing and Brain-Inspired Computing

This new reaction method allows multiple ultrasmall pores to form within a single nanopore. It offers a powerful way to study how ions and fluids move in extremely confined environments similar to those found in biology.

The chemically driven membrane system could also support emerging technologies such as single-molecule sensing (e.g., using nanopores to sequence DNA), neuromorphic computing (using electrical spikes to mimic the behavior of biological neurons), and nanoreactors (creating unique reaction conditions through confinement).

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Monday, March 23, 2026

Scientists Unveil Cheaper and Faster Way To Extract Lithium From Massive Untouched Reserves




A new solvent-based technique could change how lithium is extracted from brines, potentially making the process faster, cheaper, and viable in places where conventional methods fail.

Few elements are as key to the clean energy transition as lithium, and global demand for it is soaring. The metal powers the rechargeable batteries inside electric vehicles and the massive storage systems that allow solar and wind energy to supply electricity long after the sun sets and the wind calms.
Unfortunately, current methods for producing lithium are slow and require high-quality feedstocks found in relatively few locations on Earth.

Ironically, the environmental costs are also significant. Refining the mineral behind clean energy requires large amounts of land and can pollute water supplies that local communities depend on.

In a new paper, researchers from Columbia Engineering describe a method for extracting lithium that could dramatically shorten processing times, unlock reserves that existing methods cannot access, and reduce environmental impact. Their technique uses a temperature-sensitive solvent to extract lithium directly from brines found in deposits around the world.

Unlike current technologies, this approach can efficiently extract lithium even when it is present in very low concentrations or mixed with chemically similar materials.

The results, detailed in a paper published in Joule, show that the innovation called switchable solvent selective extraction, S3E (pronounced S three E) can extract lithium with strong selectivity: up to 10 times higher than for sodium and 12 times higher than for potassium. The process also excludes magnesium, a common contaminant in lithium brines, by triggering a chemical precipitation step that separates it out.

Improving on Solar Evaporation

Roughly 40% of global lithium production begins with salty brines stored in large underground reservoirs beneath deserts. Nearly all of that lithium is extracted using a technique called solar evaporation, in which brine is pumped into sprawling ponds that bake under the desert sun sometimes for up to two years until enough water evaporates.

This approach is only feasible in dry, flat regions with vast areas of land, such as Chile’s Atacama Desert or parts of Nevada. It also consumes large volumes of water in places that can scarcely afford it.

“There’s no way solar evaporation alone can match future demand,” said Ngai Yin Yip, La Von Duddleson Krumb Associate Professor of Earth and Environmental Engineering at Columbia University. “And there are promising lithium-rich brines, like those in California’s Salton Sea, where this method simply can’t be used at all.”

Unlike conventional lithium recovery methods, S3E does not rely on binding chemicals or extensive post-processing. Instead, the process exploits how lithium ions interact with water molecules in a solvent system that changes its behavior with temperature.

At room temperature, the solvent pulls lithium and water from the brine. When heated, it releases the lithium, along with water, into a purified stream and regenerates itself for reuse.

An Approach with Tremendous Potential

In laboratory tests using synthetic brines modeled on the Salton Sea, a geothermal region in Southern California estimated to contain enough lithium to supply more than 375 million EV batteries, the system recovered nearly 40% of the lithium after just four cycles using the same solvent batch. That performance suggests a potential path toward continuous operation.

“This is a new way to do direct lithium extraction,” said Yip. “It’s fast, selective, and easy to scale. And it can be powered by low-grade heat from waste sources or solar collectors.”

The team emphasized that this is a proof-of-concept study. The system hasn’t yet been optimized for yield or efficiency. But even in this early form, S3E appears promising enough to offer an alternative to evaporation ponds and hard-rock mining, the two approaches that dominate the lithium supply chain today and come with steep tradeoffs.

As the global clean energy transition picks up speed, technologies like S3E could play a crucial role in keeping it on track by making it possible to extract lithium faster, more cleanly, and from more places than ever before.

“We talk about green energy all the time,” said Yip. “But we rarely talk about how dirty some of the supply chains are. If we want a truly sustainable transition, we need cleaner ways to get the materials it depends on. This is one step in that direction.”

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Friday, March 20, 2026

Scientists Solve a Long-Standing Chemistry Challenge With Light-Driven Catalysis



Chemists have developed a light-driven method for producing a rare and highly strained molecular structure known as “housane.”

Designing a new drug often starts with a basic but difficult task: making the exact molecular framework needed for a medicine to work. Some important drugs, including penicillin, depend on tiny ring-shaped structures made from three or four connected atoms. Although these compact motifs can have an outsized effect on biological activity, they are not always easy to build in a practical way.

Researchers led by Prof. Frank Glorius at the Institute of Organic Chemistry at the University of Münster have developed a new approach that converts simple and widely available starting materials into these compact ring structures with high efficiency. The resulting molecule has a shape that resembles a simple drawing of a house, which is why chemists refer to it as “housane.” The transformation relies on a photocatalyst that absorbs light and transfers that energy to the reacting molecules, allowing the chemical change to occur.

These small ring systems store a large amount of internal strain, similar to the tension in a bent branch. When that tension is released, it can drive additional chemical reactions. Because of this property, strained ring molecules are useful building blocks for creating more complex and valuable compounds. Despite their usefulness, producing molecules that contain this level of strain has proven challenging.

Earlier strategies for making housane often relied on “harsh” reaction conditions, including very high temperatures. Another limitation is that those methods generally do not tolerate many additional atoms or groups of atoms attached to the starting materials. Chemists refer to these attachments as functional groups, and they strongly influence the behavior and properties of a molecule.

Controlling Light-Driven Reactions

To solve this problem, the team turned to hydrocarbons known as (1,4-dienes). Under light, these molecules usually head off in the wrong direction, producing unwanted side reactions instead of the desired product. The researchers found that by adjusting the side chains on the starting materials, they could steer the chemistry away from those competing pathways and make the process much more selective.

Once those detours were blocked, the molecules were able to fold into the tense ring system needed to form housane. “This process is normally difficult to achieve because it is energetically ‘uphill’ and requires additional momentum. Photocatalysis provides the necessary energy,” Frank Glorius explains. Computer-aided analyses helped the team map out how the reaction proceeds, offering a clearer picture of why the method works.

Computer-aided analysis also helped the researchers clarify how the reaction proceeds at the molecular level.

The technique allows chemists to produce housane more easily and with greater efficiency. It also increases the ways in which this highly strained framework can be used to assemble more complex molecules. According to the researchers, the approach could support both fundamental chemical research and practical applications, including pharmaceutical manufacturing and the development of new materials.

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Wednesday, March 18, 2026

Unlocking Potassium Battery Secrets! #worldresearchawards #Analyticalchemistry#researchawards

 


This study investigates a transient intermediate state that governs the formation and composition of the solid electrolyte interphase in potassium batteries. Understanding this mechanism provides insights into interfacial stability, enhancing battery performance, lifespan, and safety for next-generation energy storage systems.

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Tuesday, March 17, 2026

A Cambridge Lab Mistake Reveals a Powerful New Way to Modify Drug Molecules





A surprising lab discovery reveals a light-powered way to tweak complex drugs faster, cleaner, and later in development.

Researchers at the University of Cambridge have created a new technique for altering complex drug molecules using light instead of hazardous chemicals. The advance could speed up drug development and improve how medicines are produced.

The work, published today (March 12) in Nature Synthesis, introduces what the researchers describe as an “anti-Friedel–Crafts” reaction. In traditional Friedel–Crafts chemistry, powerful reagents or metal catalysts are required under demanding laboratory conditions. Because of these harsh requirements, the reaction typically takes place early in the manufacturing process, followed by many additional steps to complete the final drug.

The Cambridge method flips this approach. Instead of making changes at the beginning, scientists can now adjust drug molecules much later in the production process.

LED Light Powers a Cleaner Chemical Reaction

The reaction does not rely on heavy metal catalysts. Instead, it is activated by an LED lamp at ambient temperature. Once the light initiates the reaction, it starts a chain process that forms new carbon–carbon bonds under gentle conditions and without toxic or costly chemicals.

In practical terms, chemists can now modify a finished or nearly finished drug molecule rather than dismantling it and rebuilding it piece by piece. That conventional process can take months.

“We’ve found a new way to make precise changes to complex drug molecules, particularly ones that have been exceptionally difficult to modify in the past,” said David Vahey, first author and a PhD researcher at St John’s College, Cambridge.

“Scientists can spend months rebuilding large parts of a molecule just to test one small change. Now, instead of doing a multistep process for hundreds of molecules, scientists can start with their hit and make small modifications later on.”

“This reaction lets scientists make precise adjustments much later in the process, under mild conditions and without relying on toxic or expensive reagents. That opens chemical space that has been hard to access before and gives medicinal chemists a cleaner, more efficient tool for exploring new versions of a drug.”

Faster Drug Development With Less Waste

Reducing the number of steps in chemical synthesis lowers the amount of chemicals required, cuts energy use, and reduces environmental impact. It also saves time for chemists working to refine new medicines.

The reaction is highly selective, allowing researchers to alter one specific part of a molecule without disturbing other delicate sections. This precision is crucial in drug development, where even small structural changes can influence how well a medicine works, how it behaves inside the body, or whether it causes unwanted side effects.

The discovery also addresses one of the most fundamental tasks in chemistry: creating carbon carbon bonds. These bonds form the backbone of countless substances, from fuels to complex biological molecules.

Because the reaction tolerates many different chemical groups on a molecule, a property chemists call “high functional-group tolerance,” it is particularly useful for late-stage optimization. This phase of drug development involves fine-tuning molecules to improve their effectiveness and safety.

By avoiding heavy metal catalysts and reducing lengthy synthetic processes, the approach could also significantly cut chemical waste and energy use in pharmaceutical manufacturing. This is increasingly important as the industry works to reduce its environmental footprint.

Inspiration From Sustainable Chemistry

Vahey works in the research group of Professor Erwin Reisner at Cambridge. Reisner’s team is known for developing chemistry systems inspired by photosynthesis. Their work often focuses on using sunlight to convert waste, water, and the greenhouse gas carbon dioxide into useful chemicals and fuels.

Reisner, Professor of Energy and Sustainability in the Yusuf Hamied Department of Chemistry and lead author of the study, said the importance of the discovery lies in expanding what chemists can accomplish under practical conditions while supporting greener chemical production.

“This is a new way to make a fundamental carbon–carbon bond, and that’s why the potential impact is so great. It also means chemists can avoid an undesirable and inefficient drug modification process.”

The researchers tested the reaction on a wide variety of drug-like molecules and showed that it can work in continuous-flow systems often used in industrial production. Collaboration with AstraZeneca helped evaluate whether the method could meet the real-world requirements of large-scale pharmaceutical development.

“Transitioning the chemical industry to a sustainable industry is arguably one of the most difficult parts of the whole energy transition,” explained Reisner.

A Breakthrough Born From a Failed Experiment

The discovery emerged from a laboratory setback, a pattern seen in several well-known scientific breakthroughs, including X-rays, penicillin, Viagra, and modern weight-loss medications.

“Failure after failure, then we found something we weren’t expecting in the mess – a real diamond in the rough. And it is all thanks to a failed control experiment,” Vahey said.

He had been testing a photocatalyst, but removed it during a control experiment. Surprisingly, the reaction still worked and sometimes performed even better without the catalyst.

At first, the unusual product appeared to be an error. Instead of discarding the result, the researchers decided to investigate it further. Reisner said this decision was critical.

“Recognising the value in the unexpected is probably one of the key characteristics of a successful scientist,” he said.

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Monday, March 16, 2026

Unlocking Agarwood's Secrets with Science! #worldresearchawards #Analyticalchemistry #research

 


This study explores the thermal release dynamics and pyrolysis signatures of Agarwood using gas-liquid microextraction coupled with Gas Chromatography–Mass Spectrometry to identify volatile compounds, providing insights into aroma formation, chemical characterization, and quality evaluation relevant to natural product chemistry and analytical science.

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Saturday, March 14, 2026

Scientists May Have Found a Way to Fix Green Hydrogen’s Biggest Problem



A new European project aims to reinvent green hydrogen without toxic PFAS or costly rare metals.

Green hydrogen is widely viewed as a crucial piece of the global shift toward cleaner energy. However, producing it at scale still presents major economic and environmental challenges. One of the most promising methods, PEM (proton exchange membrane) electrolysis, is well-suited for generating hydrogen when renewable electricity from wind and solar fluctuates. Despite that advantage, the process remains significantly more expensive than hydrogen production based on fossil fuels.

There are also sustainability concerns tied to the technology. Current PEM systems rely on substances known as forever chemicals (PFAS), which are considered environmentally harmful and are expected to face restrictions in the European Union. A new European research initiative called SUPREME aims to solve these problems. Over the next three years, an international team led by the University of Southern Denmark and involving Graz University of Technology (TU Graz) will work on a PFAS-free electrolysis technology that is both highly efficient and less dependent on scarce materials such as iridium. The goal is to lower costs while improving environmental safety.

Hydrogen’s Growing Role in Industry and Energy Storage

“Hydrogen is used as a raw material in very large quantities, and this will continue to increase in the future. These include the production of ammonia, methanol production, and the steel industry,” says Merit Bodner from the Institute of Chemical Engineering and Environmental Technology at TU Graz.

“If we succeed in avoiding the use of harmful substances in the production of green hydrogen and we can also bring it to a similar price level as fossil hydrogen in economic terms, we will have taken an important step towards the green transition. This also makes it more attractive for other applications, such as storing surplus energy from renewables.”

Hydrogen already plays a critical role in several major industries, and demand is expected to keep rising. Making green hydrogen more affordable and environmentally responsible could expand its use even further, including helping store excess energy generated by renewable sources.

Testing PFAS Free Materials for Industrial Electrolysis

TU Graz plays a key role in the SUPREME project. The research group led by Merit Bodner is examining which PFAS-free materials are already available on the market and how they perform compared with existing industry standards. A major focus is determining whether these more sustainable alternatives can deliver the same durability and efficiency required for long term industrial operation.

At the same time, the Turkish Science and Technology Council TÜBITAK is developing the next generation of microporous PFAS-free membranes. These membranes will be designed for use in advanced electrolysis systems.

Cutting Iridium Use and Boosting Recycling

Another central objective of the project is reducing dependence on iridium, a rare and expensive platinum group metal used in PEM electrolysis. Researchers at the University of Southern Denmark and the British metal and catalyst company Ceimig are investigating ways to lower iridium use by up to 75 percent. They are also working on processes that could recycle about 90 percent of the iridium still required.

Other partners are contributing key components of the system. Fraunhofer ISE in Germany is responsible for producing the membrane electrode units, while the Norwegian hydrogen company Element One Energy AS (EoneE) is developing a new rotating electrolyser design.

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Friday, March 13, 2026

New Catalyst Turns CO2 Into Valuable Methanol With Unprecedented Efficiency



A new catalyst built from isolated indium atoms allows scientists to convert CO2 into methanol more efficiently while revealing the hidden chemistry that drives the reaction.

Methanol is an important building block for many chemical products. Scientists at ETH Zurich have now developed a highly efficient method for producing this compound from carbon dioxide (CO2) and hydrogen by using catalysts made from individual metal atoms.

Every chemical reaction must overcome an energy barrier before it can occur. In simple situations, this barrier can be relatively small. Striking a match, for example, provides enough energy to start a reaction. In many industrial processes, however, the required energy is much higher. Supplying that energy increases operating costs.

To make reactions easier to start, chemists rely on catalysts. These substances speed up chemical reactions without being consumed in the process. Many of the most effective catalysts contain metals, including some that are rare and expensive.

Better, more efficient, and leaving nothing to chance

Chemists have now reported a major advance in catalyst research:
  • The team created a catalyst that greatly lowers the energy needed to produce methanol, an alcohol, from the greenhouse gas CO2 and hydrogen.
  • Their design uses the metal indium in an extremely efficient way. Each individual indium atom acts as an active site where the chemical reaction occurs.
  • The catalyst also provides scientists with a clearer view of the chemical processes happening on its surface. In the past, catalyst development often relied on trial and error. The new system allows researchers to study reaction mechanisms more precisely, which could support a more systematic approach to designing future catalysts.
The Swiss army knife of green chemistry

“Methanol is a universal precursor for the production of a wide range of chemicals and materials, such as plastics the Swiss army knife of chemistry, so to speak,” says Javier Pérez-Ramírez, Professor of Catalysis Engineering at ETH Zurich. The liquid therefore plays a vital role in the transition to sustainable and fossil-free production of chemical products and fuels.

Because methanol can be transformed into fuels, plastics, and many other products, it plays an important role in efforts to shift toward more sustainable and fossil-free manufacturing.

If the hydrogen required for the reaction and the energy that drives the catalytic process are produced using renewable sources, methanol itself could be made in a climate-neutral way. In that case, CO2 from the atmosphere would become a raw material rather than simply a waste product released into the air.

Maximum use of the metals

“Our new catalyst has a single atom architecture, in which isolated active metal atoms are anchored on the surface of a specially developed support material,” Pérez-Ramírez explains. In conventional catalysts, on the other hand, metals are usually present as aggregates, usually small particles. Although these particles are tiny, they often contain between a hundred and several thousand metal atoms.

In conventional catalysts, metals are typically present as clusters or nanoparticles. Even though these particles are extremely small, each one can contain anywhere from a hundred to several thousand metal atoms. Only the atoms on the surface actively participate in the reaction.

Single-atom catalysts aim to eliminate that inefficiency. By dispersing metals as individual atoms, researchers can maximize the use of scarce and costly elements. In some cases, this strategy could even make precious metals economically practical for large-scale industrial use.

Working at the level of single atoms can also change how a metal behaves chemically. “Indium has already been used in this catalyst for over a decade,” says Pérez-Ramírez. “In our study, we show that isolated indium atoms on hafnium oxide allow more efficient CO2-based methanol synthesis than indium in the form of nanoparticles containing large numbers of atoms.”

Single atoms in the right place

Securing individual indium atoms onto a hafnium oxide surface required careful engineering. The interdisciplinary ETH team developed several synthetic routes in collaboration with researchers from other institutions.

A critical factor was the design of the support material. Its structure provides a setting that is both stable and chemically active, allowing the isolated atoms to remain in place while still participating in the reaction.

In one manufacturing approach tested by the researchers, the starting materials are burned in a flame at temperatures between 2,000 and 3,000°C (about 3,600 to 5,400°F) and then cooled very rapidly. Under these extreme conditions, indium atoms tend to stay on the surface, where they become firmly embedded.

By incorporating the metal atoms into a heat-resistant hafnium oxide support, the scientists demonstrated that single-atom catalysts can remain stable even under demanding conditions. This is crucial because industrial methanol production from CO2 and hydrogen requires temperatures of up to 300°C (about 572°F) and pressures up to 50 times normal atmospheric pressure.
Interaction between the catalyst metal and the matrix

Another advantage of single-atom catalysts is that they are easier to analyze.

With traditional nanoparticle catalysts, most measurement signals come from atoms inside the particles, even though only surface atoms drive the reaction. This makes it difficult to determine exactly what is happening during the process.

In contrast, when metals are dispersed as isolated atoms, there are far fewer extraneous signals. Researchers can more clearly observe the reaction mechanisms taking place.

Pérez-Ramírez has been investigating improved catalysts for methanol production from CO2 at ETH since 2010. He also collaborates closely with industry and holds several patents in this field.

According to Pérez-Ramírez, the strong network of catalysis research in Switzerland played a central role in this achievement. “The development of the methanol catalyst and the detailed analysis of the mechanism would not have been possible without this interdisciplinary expertise.”

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Thursday, March 12, 2026

Scientists Map the Hidden Chemistry of Solar-Powered Catalysts




A new computational approach reveals how subtle structural changes in polyheptazine imides can dramatically influence their ability to convert sunlight into chemical energy.

Photocatalysis offers a promising way to convert abundant sunlight into useful chemical energy. Among the materials attracting attention for this purpose are polyheptazine imides, which possess distinctive structural and functional features that make them strong candidates for solar-driven chemical reactions. Until recently, however, scientists had only a limited understanding of how structural variations influence the electronic and optical behavior of the many materials in this class.

Researchers led by a team from the Center for Advanced Systems Understanding (CASUS) at Helmholtz-Zentrum Dresden-Rossendorf (HZDR) have now developed a dependable theoretical approach that addresses this challenge. Their method produces consistent predictions and was validated through experiments on real polyheptazine imide materials. The researchers believe their findings could significantly accelerate research and development in this field.

Polyheptazine imides belong to the carbon nitride family, a group of layered compounds that resemble graphene in structure. These materials are made from nitrogen-rich ring-shaped building blocks that stack into sheets. Unlike graphene, which conducts electricity extremely well but lacks photocatalytic activity, polyheptazine imides have band gaps that allow them to absorb visible light.

Carbon nitride materials are appealing for practical use because they are inexpensive to manufacture, non-toxic, and thermally stable. However, early versions of these materials performed poorly as photocatalysts because their electronic properties made charge separation inefficient.

When charge separation is weak, an electron excited by incoming light quickly recombines with the hole it left behind. Instead of driving a chemical reaction, the absorbed energy is released as heat or light. “Polyheptazine imides containing positively charged metal ions exhibit markedly improved charge separation. This feature renders them highly suitable for practical applications,” says first author Dr. Zahra Hajiahmadi.

Computer science narrows down options

Improved materials are needed to unlock the economic potential of photocatalytic reactions. Examples include splitting water to produce hydrogen fuel, reducing carbon dioxide to create basic carbohydrates that can serve as fuels or industrial chemicals, and producing hydrogen peroxide, which is widely used in industry.

Designing a polyheptazine imide that efficiently drives a specific reaction requires careful control of many structural details. Testing every possible material combination through laboratory synthesis alone would be impractical. Computational modeling, therefore, plays a crucial role in guiding the search.

“The design space is enormous,” says Prof. Thomas D. Kühne, Director of CASUS, leader of the CASUS research team “Theory of Complex Systems,” and senior author of the study. “One can, for example, add functional groups on the surface or substitute specific nitrogen or carbon atoms with oxygen or phosphorus atoms.” Kühne’s research group develops advanced numerical techniques that balance computational efficiency with an accurate representation of the chemistry and physics governing these materials.

Finding the perfect material in a systematic way

Hajiahmadi’s work focused on a defining structural element of polyheptazine imides: negatively charged pores that can host positively charged metal ions. Adding these ions can significantly enhance catalytic performance.

Her study provides the first comprehensive investigation of how different metal ions affect the optoelectronic properties of polyheptazine imides. The researchers analyzed 53 metal ions in total, categorizing them based on their position within the structure, either in the plane of the layers or between them, and examining whether they caused distortions in the material’s geometry.

“We used a reliable and reproducible computational framework that goes beyond conventional modeling approaches,” says Hajiahmadi. “Standard computational studies of photocatalysts typically focus on ground-state properties and neglect excited-state effects, despite the fact that photocatalysis is inherently driven by photoexcited charge carriers. Specifically, we employ many-body perturbation theory methods.”

These techniques begin with a simplified system in which particles do not interact. Interactions between particles are then introduced as small perturbations, and their effects are calculated as corrections to the original solution. The mathematical expansions that follow allow researchers to approximate how large groups of particles influence one another. Because these calculations require significant computational resources, they are rarely used in this field. The new study demonstrates that the approach can provide a far more accurate picture of how materials absorb light and behave electronically under illumination.

Using this framework, the team systematically examined how various metal ions alter the structure of the polyheptazine imide polymer network. The analysis showed that inserting ions can produce clear structural changes, including shifts in layer spacing and modifications to the local bonding environment.

These structural adjustments directly influence the material’s electronic band structure and optical properties, including its ability to harvest light.

To test the model’s predictions, the researchers synthesized eight polyheptazine imide materials, each containing a different metal ion. The samples were then evaluated for their ability to catalyze the production of hydrogen peroxide.

“The results clearly showed a high degree of agreement to our predictions and outperformed competing calculation methods,” Hajiahmadi concludes.

Kühne adds: “If there was some doubt about polyheptazine imides being one of the most promising platforms for next-generation photocatalytic technologies, I believe this work put them to rest. The path toward the targeted design of efficient polyheptazine imide photocatalysts for sustainable reactions is clearer now. I firmly believe that it will be taken often and successfully.”

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Wednesday, March 11, 2026

Unlocking the Power of Castanopsis! #worldresearchawards #Analyticalchemistry #research

 

This study reports previously undescribed triterpenoid ellagitannins isolated from Castanopsis calathiformis. Structural characterization and bioactivity evaluation reveal promising antiproliferative and hypoglycemic properties, highlighting their potential as natural therapeutic candidates for cancer inhibition and glucose regulation.

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Saturday, March 7, 2026

Scientists Create Powerful New Form of Aluminum That Could Replace Rare Earth Metals




Researchers have uncovered an unusual new form of aluminium that challenges long-held assumptions about how this common metal behaves.

Researchers at King’s College London have identified an unusual new form of aluminum, one of the most abundant metals in Earth’s crust. The discovery points to a much less expensive and more sustainable substitute for rare earth metals that are widely used in modern technology and industry.

Dr. Clare Bakewell, a senior lecturer in the Department of Chemistry, led the study. Her team created highly reactive aluminum-based molecules capable of breaking some of the strongest chemical bonds. Their findings, published in Nature Communications, also describe molecular structures that have never been observed before, opening the door to new types of chemical reactivity.

A central achievement of the research is the first reported example of a cyclotrialumane. This compound consists of three aluminum atoms linked together in a triangular arrangement. The three-atom structure shows an unusual level of reactivity while remaining intact when dissolved in different solutions.

That stability allows it to participate in a variety of chemical processes. Among them are the splitting of dihydrogen and the controlled insertion and chain growth of ethene, a 2-carbon hydrocarbon that serves as a key building block in chemical manufacturing.

Reducing Dependence on Precious Metals

Metals play an essential role in producing both bulk and specialty chemicals. However, many industrial reactions, especially those involving catalysis, depend on precious metals such as platinum. Mining and refining these materials is costly and can cause significant environmental harm.

Scientists have long been searching for alternative metals to use in chemical transformations. Dr. Clare Bakewell said: “Transition metals are the workhorses of chemical synthesis and catalysis – but many of the most useful are becoming increasingly difficult to access and extract often being located in regions of political instability, increasing the demand and price.

“Chemists have been looking towards more common elements from the periodic table, and we chose aluminum, as it’s super abundant, making it ~20,000 times less expensive than precious metals such as platinum and palladium.”

Beyond Mimicking Transition Metals

Beyond designing aluminum compounds for synthetic applications, the team has uncovered entirely new reaction pathways.

Dr. Bakewell said, “What’s special about this work, is that we’re pushing the boundaries of chemical knowledge. Most excitingly, we can use this aluminum trimer to build completely new compounds with levels of reactivity that have never been observed before – these include the 5- and 7-membered aluminum and carbon rings formed through reaction with ethene. These capabilities go beyond the transition metals we were originally trying to mimic, to the forefront of chemical research.”

Bakewell believes this chemistry could enable scientists to invent new reaction types and assemble larger molecular structures with distinctive properties. Such advances may ultimately support the development of new materials and industrial products.

She said, “We’re very much in the exploratory phase, and we’re just at the start of beginning to unlock the capability of these earth-abundant materials.

“But from what we’ve seen already, this chemistry could support a transition to cleaner, greener and cheaper chemical production, whilst making new discoveries along the way.”

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Friday, March 6, 2026

Scientists Uncover the Secret Structure Behind “Nature’s Proton Highway”




By freezing a crucial phosphoric acid complex to near absolute zero, scientists uncovered a single, unexpectedly stable structure at the heart of proton transport.

Phosphoric acid is vital in both biology and modern technology because of its exceptional ability to move electrical charge. Inside the human body and in devices such as fuel cells, this small molecule helps drive essential chemical reactions.

Scientists at the Department of Molecular Physics at the Fritz Haber Institute have now uncovered new details about how it performs this task at the molecular level.

How Tiny Electrical Signals Control Life

Every second, countless electrical charges flow through our bodies. These signals are essential for life. Processes such as cellular communication, energy conversion, and metabolism all rely on the carefully controlled movement of charged particles across membranes and within cells. In many ways, the transport of charge serves as a fundamental regulatory system.

Phosphoric acid (H3PO4) and related phosphate compounds are found throughout living organisms. They form the backbone of DNA and RNA, contribute to the structure of cell membranes, and are part of ATP, the molecule that stores and delivers energy in cells. These compounds are especially important for moving positive charges in biological systems.

Beyond biology, phosphoric acid also plays a significant technological role. It is used in certain types of batteries and in fuel cells. In these systems, engineers take advantage of one standout feature: its unusually high proton conductivity.

Protons carry a positive charge and can move through phosphate-containing materials in a stepwise fashion. They “jump” from one molecule to the next along networks of hydrogen bonds. This process, known as “proton-shuttling”, enables charges to travel extremely quickly.

Although scientists have long understood that this mechanism operates, many of its finer details have remained unclear. In their recent study, researchers from the Fritz Haber Institute, working with collaborators in Leipzig and the USA, focused on determining the structure of a crucial negatively charged phosphoric acid complex. By clarifying its structure, they aimed to better understand the earliest stages of proton transfer.

A Cold Look at Hot Chemistry with Cryogenic Spectroscopy

Earlier research suggested that a specific negatively charged form of phosphoric acid could act as the starting point for the proton-shuttling sequence. This species is the deprotonated dimer H3PO4·H2PO4-.

To examine it more closely, the team created this molecule in the laboratory and studied it under extremely cold conditions. They embedded it inside a helium nanodroplet, cooling it to just 0.37 degrees above absolute zero. Using infrared radiation, they then analyzed its structure.

Cooling the molecule to such low temperatures greatly reduces thermal motion and other disturbances. This allows scientists to measure its structure with high precision. The experimental findings were further supported by quantum chemical calculations, which help predict how molecules are arranged and how they behave.

The Invisible Network: Structure and Hydrogen Bonds Found

When the researchers compared their measurements with theoretical predictions, they found only partial agreement. Computational models had suggested that two structural forms should be equally likely. However, the experimental results clearly showed that the deprotonated phosphoric acid dimer adopts a single stable structure.

This structure is relatively rigid and presents high energy barriers for proton transfer. It contains three hydrogen bonds and features a shared oxygen atom that serves as an acceptor. Similar arrangements have been observed in other phosphoric acid-containing clusters, indicating that this hydrogen-bonding pattern may be common in such systems.

The findings demonstrate that theoretical models alone may not always capture the full picture. Careful experimental work remains essential for determining accurate molecular structures.

Why It Matters

The study offers new insight into the molecular basis of phosphoric acid’s remarkable proton conductivity, “Nature’s proton highway.” By identifying a single stable structure for the key anionic dimer H3PO4·H2PO4- and revealing its distinct hydrogen-bonding motif, the researchers have clarified an important piece of the proton transport puzzle.

In addition, the work provides a valuable reference point for improving quantum chemical methods used to model phosphate-containing clusters. These advances could support the development of better proton-conducting materials and deepen scientific understanding of how proton transfer operates in living systems.

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Thursday, March 5, 2026

What Do Mummies Smell Like? Scientists Unlock 2,000-Year-Old Secrets




Chemical analysis of mummy scents reveals evolving embalming recipes in ancient Egypt. Advanced air sampling detected dozens of compounds, showing increasing sophistication and enabling safer study of fragile remains.

For centuries, mummification has fascinated historians and archaeologists. Now, researchers report that the characteristic musty odor of preserved bodies contains valuable scientific clues. Rather than being simply the result of aging, the smell reflects a blend of embalming substances and treated linens that document how techniques developed over time.

The study was led by chemists at the University of Bristol, who found that the distinctive scent is closely tied to the materials used during embalming.

According to lead author Dr. Wanyue Zhao, Research Associate in Organic Geochemistry at the University of Bristol, “The findings mark a significant step forward in improving our understanding of Egyptian history and the fascinating ritual of mummification. Our analysis of the associated scents has uncovered new insights into how the practice developed through the ages and became increasingly sophisticated.”

Non-Destructive Techniques Capture Volatile Organic Compounds

To carry out the research, the team analyzed the air surrounding tiny mummy fragments about the size of a peppercorn. Conventional approaches often involve dissolving samples with solvents, which can harm fragile artifacts. Instead, the scientists focused on capturing gases released into the surrounding air.

Using solid-phase microextraction together with gas chromatography and high-resolution mass spectrometry, they collected and separated the airborne chemicals, referred to as volatile organic compounds (VOCs), for detailed examination.

Chemical Signatures of Fats, Resins, Beeswax, and Bitumen

Even when present in trace amounts, these compounds could be grouped into four main categories linked to specific materials. Fats and oils generated aromatic compounds and short-chain fatty acids. Beeswax produced monocarboxylic fatty acids and cinnamic compounds. Plant resins emitted aromatic compounds and sesquiterpenoids, while bitumen released naphthenic compounds.

Dr. Zhao explained that the chemical patterns shifted over time. “Our findings showed the chemical patterns varied across historical periods. Earlier mummies had simpler profiles dominated by fats and oils, while later mummies displayed more complex mixtures incorporating imported resins and bitumen. Such materials were more costly and required more specialized preparation, as the practice became more advanced.”

The analysis also revealed differences depending on which part of the body was sampled.

“For instance, samples from heads often contained different patterns than those from torsos, suggesting embalmers applied distinct recipes to separate parts of the body to possibly aid preservation. This is an area which needs further analysis and research to better understand what techniques were used and why,” Dr. Zhao added.

Advancing Mummification Research and Museum Preservation

Study co-author Richard Evershed, professor of chemistry at the University of Bristol, said, “Our volatile analysis proved sensitive enough to detect residues at extremely low concentrations. For example, bitumen biomarkers were previously difficult to detect with earlier soluble residue methods.

“This approach expands the study of ancient Egyptian funerary practices, presenting a clearer, fuller picture of mummification recipes, material choices, and preservation strategies.”

The technique could also assist museums and collections worldwide. Air sampling offers a fast, nondestructive way to screen fragile mummies, helping curators gather chemical data without compromising their condition.

Study co-author Ian Bull, Professor of Analytical Chemistry at the University of Bristol, added, “Physical sampling still plays a role for detailed work, yet volatile analysis provides an effective and enlightening first step for studying embalmed remains across collections and time periods.”

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Wednesday, March 4, 2026

Breakthrough Device Could Slash Ethylene’s Massive Carbon Footprint




A new electrolyzer turns waste-derived syngas into ethylene with significantly lower energy input.

Ethylene sits at the center of modern manufacturing. It is used to make plastics and many other everyday materials, but producing it often comes with a major climate penalty. For every ton of ethylene created, one ton of carbon dioxide is produced. With more than 300 million tons of ethylene produced each year, that adds up to an enormous source of emissions that researchers want to shrink and ultimately remove.

In a new study from Northwestern University, Ted Sargent’s team reports an electrolyzer designed to push ethylene production toward a cleaner model by linking waste and renewable electricity.

The device uses electricity to turn syngas into ethylene. Syngas is a mixture of carbon monoxide and hydrogen that can be made by gasifying plastic waste. That starting point matters because it can be easier to upgrade syngas into valuable chemicals than it is to build the same products directly from carbon dioxide. The researchers also introduced a new material that helps the reaction run effectively, and they built the system to cut the overall energy required.

The results, published in Nature Energy, point to a potential route for making ethylene with renewable power, reducing the need for fossil-based inputs along the supply chain.

“Our goal is to decarbonize chemicals,” Sargent said. “And this work is a big step in that direction.”

Sargent is the Lynn Hopton Davis and Greg Davis Professor of Chemistry at Northwestern’s Weinberg College of Arts and Sciences and a professor of electrical and computer engineering at Northwestern’s McCormick School of Engineering.

“We want to create a circular system that creates chemical building blocks from waste without using fossil fuels,” said Ke Xie, a research faculty member in chemistry at Weinberg. “And this system is part of that new atom-efficient and energy-efficient supply chain.”

Creating energy from waste

Today, most ethylene is made through steam cracking, a process that uses high-temperature steam to break down crude oil into smaller chemical components. While effective, this method relies heavily on fossil fuels and consumes large amounts of energy.

Scientists have been investigating ways to replace it with electricity-driven processes powered by renewable sources. One possibility is to convert carbon dioxide directly into ethylene. However, that reaction requires significant energy input, making it difficult to compete with existing industrial methods.

Instead, Sargent’s team focused on syngas, which is produced by heating plastic waste in a low-oxygen environment. Syngas contains carbon monoxide and hydrogen. Because it is chemically closer to ethylene than carbon dioxide is, transforming it into ethylene requires less electricity.

“A lot of syngas is made into chemicals, so finding a route to take the syngas to ethylene that’s both very selective and very energy efficient is of industrial interest,” Sargent said.

To make this conversion practical, the researchers needed to design a different kind of electrolyzer, a cell that uses electrical energy to drive chemical reactions. Most electrolyzers rely on liquid water mixed with dissolved salts that supply both positive and negative ions.

The team explored whether they could build a system that operates with gases on both sides of the reaction. In their design, carbon monoxide from syngas would enter on one side (the cathode), while hydrogen would be supplied on the other (the anode).

“In initial attempts, we tried to make a gas-gas electrolyzer, but it just didn’t work,” he said. “And what we realized was that we didn’t just need the water we needed the salt.”

A novel device that works with renewable energy

Salt provides the positive ions (cations) that the device’s copper catalyst needs to stabilize key intermediates in the reaction. Bosi Peng, a postdoctoral researcher in the lab and first author on the paper, searched for the right material that could trap those ions while also keeping them loose enough to react within the system.

“We needed to find a material in this Goldilocks zone to make a successful electrolyzer,” Sargent said. “And Bosi found a new way to solve this hard problem, which was really exciting.”

The material, sodium polyacrylate (PANa), creates a micro-environment within the system that mimics a liquid salt bath, while keeping the system dry of liquid water. The result is a process that is more than 60% more efficient than the most energy-efficient prior electrified processes that turn carbon dioxide into ethylene.

“Bosi significantly reduced the electricity needed by lowering the voltage we have to apply across the device,” Sargent said. Even further, the device works well with the intermittent nature of renewable energy sources.

“Solar and wind are very cheap sources of energy, but they come and go,” he said. “We needed to create a device that could deal with intermittent energy, and we found this system could do that. A key ingredient in doing so was to take out the liquid water with the high concentration salt in the electrolyte.”

Next, the team plans to try to reduce the energy consumption of the device even further, so it’s on par with energy used in steam cracking. They are also using artificial intelligence and machine learning tools to find catalysts that would make the device even more efficient.

Ultimately, the goal is to create a device that can scale up to be used in industry to continue to reduce ethylene’s carbon footprint.

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Tuesday, March 3, 2026

Quantum Chemistry Meets Pyrazole: A New Era in Energetic Materials! #worldresearchawards #chemistry

 


This research integrates quantum-chemistry calculations with Bayesian optimization to accelerate discovery of novel pyrazole-based energetic materials. By predicting performance, stability, and sensitivity, the data-driven framework efficiently guides molecular design, reducing experimental workload while enhancing safety and energetic efficiency.

 #worldresearchawards #Analyticalchemistry #research #QuantumChemistry #BayesianOptimization #EnergeticMaterials #Pyrazole #ComputationalChemistry #MaterialsDiscovery #MachineLearning #MolecularDesign #DataDrivenScience #HighEnergyMaterials #PredictiveModeling #ChemicalEngineering #AdvancedMaterials

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Unlocking Health: Resistant Starch in Bread!

  This study explores the preparation of resistant starch type 3 using glycogen debranching enzyme from Corynebacterium glutamicum and its i...