Tuesday, September 30, 2025

Alpha amino acids' stability may explain their role as early life's protein building blocks



A new study from the Hebrew University of Jerusalem published in the Proceedings of the National Academy of Sciences sheds light on one of life's greatest mysteries: why biology is based on a very specific set of amino acids, and in particular, why nature selected alpha amino acids as the foundation for proteins.

The research, led by Dr. Moran Frenkel-Pinter and her lab members Sarah Fisher and Yishi Ezerzer of the Institute of Chemistry and the Center for Nanoscience and Nanotechnology at the Hebrew University, explored the properties of depsipeptides simple model peptide-like molecules that could have formed on early Earth through natural processes.

Unlike modern peptides, depsipeptides contain a mix of ester and amide bonds, making them easier to form under prebiotic conditions but less stable over time.

Every living organism on Earth forms its proteins from the exact same set of 20 amino acids. Why that specific set? The new study suggests that life's dependence on these 20 amino acids is no accident. A key question has puzzled scientists for decades: why did life favor alpha amino acids over their beta or gamma counterparts, even though all were abundant on prebiotic Earth?

To test whether molecular assembly played a role, Frenkel-Pinter and her team synthesized depsipeptides using a wide range of hydroxy and amino acids, then observed their ability to self-assemble in solution.

The results were striking. Depsipeptides built from alpha acids readily formed stable, droplet-like assemblies that persisted for weeks, even after freezing and thawing. In contrast, beta-based assemblies, if formed, phase-separated more quickly in solution and showed significantly lower physical stability. This difference, the researchers argue, could have been a decisive factor in the evolutionary "choice" of the alpha backbone.

"Self-assembly is one of life's most fundamental prerequisites," said Dr. Frenkel-Pinter. "Our findings suggest that the superior ability of alpha-based proto-peptides to form stable compartments may have given them a crucial evolutionary edge, setting the stage for the protein backbones we see in biology today."

"The question of why evolution handpicked a specific set of amino acids has remained a mystery for a very long time. Taking even a single step toward answering this long-lasting question is remarkable, and it is a privilege to contribute to this pursuit," said Ezerzer, a master's student co-leading this project together with Fisher.

"We demonstrate here, for the first time, the ability of depsipeptides to self-assemble, similar to modern peptides. While these findings are a breakthrough in the field of chemical evolution, they may also have future implications for other fields such as the pharmaceutical industry," said Fisher.

The study marks the first time that the assembly properties of alpha and beta proto-peptide backbones have been directly compared. By demonstrating that stability at the molecular level could have influenced chemical evolution, the research proposes an assembly-driven selection model for life's earliest building blocks.

These findings add a new dimension to origins-of-life studies, suggesting that it was not just chemical reactivity but also the capacity for long-lasting self-assembly that shaped the transition from prebiotic chemistry to biology.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Unlocking Sulfonation Secrets of Acridine! #sciencefather #Analytical Ch...

Monday, September 29, 2025

Mushrooms Evolved Psychedelics Twice, and Scientists Just Found Out




Scientists have uncovered that mushrooms evolved the ability to make psilocybin not once but twice, using completely different biochemical toolkits.

This rare case of convergent evolution shows nature arriving at the same mind-altering molecule by two separate paths. The true reason fungi produce psilocybin remains unsolved, but theories range from predator defense to chemical communication. Beyond evolutionary intrigue, the discovery also offers new enzyme tools that could help produce psilocybin more efficiently for future medicines.

Ancient Molecule With a Modern Role

“This concerns the biosynthesis of a molecule that has a very long history with humans,” explains Prof. Dirk Hoffmeister, head of the research group Pharmaceutical Microbiology at Friedrich Schiller University Jena and the Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI).

“We are referring to psilocybin, a substance found in so-called ‘magic mushrooms’, which our body converts into psilocin a compound that can profoundly alter consciousness. However, psilocybin not only triggers psychedelic experiences, but is also considered a promising active compound in the treatment of therapy-resistant depression,” says Hoffmeister.

Two Evolutionary Paths to Psilocybin

The study, carried out within the Cluster of Excellence ‘Balance of the Microverse’, reveals that fungi developed the ability to produce psilocybin on at least two separate occasions in evolutionary history. Psilocybe mushrooms rely on a familiar set of enzymes to make the molecule, while fiber cap mushrooms use an entirely different biochemical toolkit. Despite these very different methods, both groups arrive at the same compound. Scientists call this convergent evolution, when unrelated species independently evolve the same trait.

Hidden Clues in Fungal Genomes

Lead author Tim Schäfer, a doctoral researcher in Hoffmeister’s lab, explains: “It was like looking at two different workshops, but both ultimately delivering the same product. In the fiber caps, we found a unique set of enzymes that have nothing to do with those found in Psilocybe mushrooms. Nevertheless, they all catalyze the steps necessary to form psilocybin.”

The team then studied these enzymes in the lab. Using protein models built by Innsbruck chemist Bernhard Rupp, they confirmed that the reaction sequence in fiber caps differs greatly from what is known in Psilocybe. “Here, nature has actually invented the same active compound twice,” notes Schäfer.

Mysteries Behind the Molecule’s Purpose

However, why two such different groups of fungi produce the same active compound remains unclear. “The real answer is: we don’t know,” emphasizes Hoffmeister. “Nature does nothing without reason. So there must be an advantage to both fiber cap mushrooms in the forest and Psilocybe species on manure or wood mulch producing this molecule we just don’t know what it is yet.”

“One possible reason could be that psilocybin is intended to deter predators. Even the smallest injuries cause Psilocybe mushrooms to turn blue through a chemical chain reaction, revealing the breakdown products of psilocybin. Perhaps the molecule is a type of chemical defense mechanism,” says Hoffmeister.

Biotech Opportunities From Fungal Chemistry

Although it is still unclear why different fungi ultimately produce the same molecule, the discovery nevertheless has practical implications: “Now that we know about additional enzymes, we have more tools in our toolbox for the biotechnological production of psilocybin,” explains Hoffmeister.

Schäfer is also looking ahead: “We hope that our results will contribute to the future production of psilocybin for pharmaceuticals in bioreactors without the need for complex chemical syntheses.” At the Leibniz-HKI in Jena, Hoffmeister’s team is working closely with the Bio Pilot Plant, which is developing processes for producing natural products, such as psilocybin, on an industrial scale.

Unlocking Nature’s Hidden Strategies

At the same time, the study provides exciting insights into the diversity of chemical strategies used by fungi and their interactions with their environment. It thus addresses central questions of the Collaborative Research Center ChemBioSys and the Cluster of Excellence ׅ‘Balance of the Microverse’ at Friedrich Schiller University Jena, within the framework of which the work was carried out and funded by the German Research Foundation (DFG), among others. While the CRC ChemBioSys investigates how natural compounds shape biological communities, the Cluster of Excellence focuses on the complex dynamics of microorganisms and their environment.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Eco-Friendly Pesticide Extraction Hack! #sciencefather #Analytical Chemi...

Saturday, September 27, 2025

Smart Film: Meat Freshness Game-Changer! #sciencefather #Analytical Chem...

Hydroxylamine discovery complicates water purification efforts

Hydroxylamine, a reactive inorganic compound and potential carcinogen, has been identified as a key intermediate in the catalytic reduction of nitrogenous pollutants. The finding raises concerns for researchers developing water purification catalysts, as it suggests that some treatment processes might inadvertently introduce hydroxylamine into drinking water.

Nitrate and nitrite enter water systems through inorganic fertilisers and can lead to health conditions such as methaemoglobinaemia in children. Consequently, the European Union has mandated a concentration limit of 50mg/l and 0.5mg/l for nitrate and nitrite in drinking water, respectively.

While there has been extensive research into developing metal catalysts for removing nitrate and nitrite from water, incomplete mass balance calculations mean these studies had not fully elucidated the role of hydroxylamine as an intermediate before. ‘The issue with this reaction is that you have gas phase products and liquid phase products,’ comments Janek Betting, who led the study. ‘Typically, this reaction is done at relatively low nitrate and nitrite concentrations of less than 1mmol/l and a tiny nitrogen leak can mess up your mass balance.’

Now, Betting and colleagues Jimmy Faria Albanese and Leon Lefferts at the University of Twente in the Netherlands have studied the extent to which hydroxylamine accumulates during nitrate and nitrite reduction over metal catalysts. The researchers used benzaldehyde to trap the hydroxylamine, which formed during the reaction and quantified the resulting oxime with liquid chromatography. Crucially, they noted that hydroxylamine accumulated during the reduction reaction and accounted for up to 56% of the reaction mixture as the reaction progressed before being converted to nitrogen and ammonia, depending on the metal catalyst they used.

‘I was surprised the percent conversion to hydroxylamine was as high as it was for the different catalyst formulations,’ comments Charles Werth, an expert in civil and environmental engineering at the University of Texas at Austin in the US.

This hydroxylamine intermediate now presents a challenge for both catalysis researchers and chemical engineers. ‘I think investigating which catalyst formulations give rise to fast hydroxylamine kinetics is an important next step,’ continues Werth. ‘The water quality conditions may also affect how the hydroxylamine intermediate persists … its production might be affected in the presence of other constituents in water. When we think about scale-up, it’s going to be important to design a reactor with hydroxylamine explicitly in mind to ensure that it isn’t discharged into treated water.’

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Friday, September 26, 2025

From chemistry to life: Building synthetic cells with metabolism


At some point during the evolution of life on Earth, inorganic matter became organic, nonliving matter became living. How this happened is one of humankind's greatest mysteries. Today, scientists work to develop synthetic cells that mimic living cells, hoping to uncover clues that will help answer the question: how did life on Earth begin?

While there's no single definition of life, three elements recur across biology:
  • compartmentalization – a barrier that separates a cell's interior from the environment;
  • metabolism – building up and breaking down molecules to carry out cell function; and
  • selection – a process in which certain molecules are favored over others.
In the past, researchers have focused on compartmentalization, but not on metabolism. Yet this cycle of building up and breaking down molecules is a critical aspect of how living cells respond to environmental stimuli, replicate and evolve.

Now researchers from the University of California San Diego have designed a system that synthesizes cell membranes and incorporates metabolic activity.

Lipids are fatty compounds that play a crucial role in many cell functions. In living cells, lipid membranes serve as barriers, separating cells from the external environment. Lipid membranes are dynamic, capable of remodeling themselves in response to cellular demands.

As a crucial step in understanding how living cells evolved, Devaraj's lab designed a system where lipids can not only form membranes, but through metabolism, can also break them down. The system they created was abiotic, meaning only nonliving matter was used. This is important in helping understand how life emerged on prebiotic Earth, when only nonliving matter existed.

"We are trying to answer the fundamental question: what are the minimal systems that have the properties of life?" said Alessandro Fracassi, a postdoctoral scholar in Devaraj's lab and first author on the paper.

The chemical cycle they created uses a chemical fuel to activate fatty acids. The fatty acids then couple with lysophospholipids, which generate phospholipids. These phospholipids spontaneously form membranes, but in the absence of fuel, they break down and return to the fatty acid and lysophospholipid components. The cycle begins anew.

Now that they've shown they can create an artificial cell membrane, they want to continue adding layers of complexity until they have created something that has many more of the properties we associate with "life."

"We know a lot about living cells and what they're made of," stated Fracassi. "But if you laid out all the separate components, we don't actually understand how to put them together to make the cell function as it does. We're trying to recreate a primitive yet functional cell, one layer at a time."

In addition to shedding light on how life may have begun in an abiotic environment, the development of artificial cells can have a real-world impact. Drug delivery, biomanufacturing, environmental remediation, biomimetic sensors are all possibilities over the coming decades as we continue to deepen our understanding of how life on Earth came to be.

"We may not see these kinds of advancements for 10 or 20 years," Devaraj noted. "But we have to do the work today, because we still have so much to learn."

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Unlocking Acetone Detection with In2O3! #sciencefather #Analytical Chemi...

Thursday, September 25, 2025

Plasticizers: From Impact to Innovation! #sciencefather #Analytical Chem...

A simple metal could solve the world’s plastic recycling problem




A new nickel-based catalyst could revolutionize recycling by turning everyday single-use plastics into useful products without tedious sorting. Credit: Shutterstock

The future of plastic recycling may soon get much less complicated, frustrating and tedious.

In a new study, Northwestern University chemists have introduced a new plastic upcycling process that can drastically reduce or perhaps even fully bypass the laborious chore of pre-sorting mixed plastic waste.

The process harnesses a new, inexpensive nickel-based catalyst that selectively breaks down polyolefin plastics consisting of polyethylenes and polypropylenes the single-use kind that dominates nearly two-thirds of global plastic consumption. This means industrial users could apply the catalyst to large volumes of unsorted polyolefin waste.

When the catalyst breaks down polyolefins, the low-value solid plastics transform into liquid oils and waxes, which can be upcycled into higher-value products, including lubricants, fuels and candles. Not only can it be used multiple times, but the new catalyst can also break down plastics contaminated with polyvinyl chloride (PVC), a toxic polymer that notoriously makes plastics "unrecyclable."

"One of the biggest hurdles in plastic recycling has always been the necessity of meticulously sorting plastic waste by type," said Northwestern's Tobin Marks, the study's senior author. "Our new catalyst could bypass this costly and labor-intensive step for common polyolefin plastics, making recycling more efficient, practical and economically viable than current strategies."

"When people think of plastic, they likely are thinking about polyolefins," said Northwestern's Yosi Kratish, a co-corresponding author on the paper. "Basically, almost everything in your refrigerator is polyolefin based squeeze bottles for condiments and salad dressings, milk jugs, plastic wrap, trash bags, disposable utensils, juice cartons and much more. These plastics have a very short lifetime, so they are mostly single-use. If we don't have an efficient way to recycle them, then they end up in landfills and in the environment, where they linger for decades before degrading into harmful microplastics."

A world-renowned catalysis expert, Marks is the Vladimir N. Ipatieff Professor of Catalytic Chemistry at Northwestern's Weinberg College of Arts and Sciences and a professor of chemical and biological engineering at Northwestern's McCormick School of Engineering. He is also a faculty affiliate at the Paula M. Trienens Institute for Sustainability and Energy. Kratish is a research assistant professor in Marks' group, and an affiliated faculty member at the Trienens Institute. Qingheng Lai, a research associate in Marks' group, is the study's first author. Marks, Kratish and Lai co-led the study with Jeffrey Miller, a professor of chemical engineering at Purdue University; Michael Wasielewski, Clare Hamilton Hall Professor of Chemistry at Weinberg; and Takeshi Kobayashi a research scientist at Ames National Laboratory.

The polyolefin predicament

From yogurt cups and snack wrappers to shampoo bottles and medical masks, most people interact with polyolefin plastics multiple times throughout the day. Because of its versatility, polyolefins are the most used plastic in the world. By some estimates, industry produces more than 220 million tons of polyolefin products globally each year. Yet, according to a 2023 report in the journal Nature, recycling rates for polyolefin plastics are alarmingly low, ranging from less than 1% to 10% worldwide.

The main reason for this disappointing recycling rate is polyolefin's sturdy, stubborn composition. It contains small molecules linked together with carbon-carbon bonds, which are famously difficult to break.

"When we design catalysts, we target weak spots," Kratish said. "But polyolefins don't have any weak links. Every bond is incredibly strong and chemically unreactive."

Problems with current processes

Currently, only a few, less-than-ideal processes exist that can recycle polyolefin. It can be shredded into flakes, which are then melted and downcycled to form low-quality plastic pellets. But because different types of plastics have different properties and melting points, the process requires workers to scrupulously separate various types of plastics. Even small amounts of other plastics, food residue or non-plastic materials can compromise an entire batch. And those compromised batches go straight into the landfill.

Another option involves heating plastics to incredibly high temperatures, reaching 400 to 700 degrees Celsius. Although this process degrades polyolefin plastics into a useful mixture of gases and liquids, it's extremely energy intensive.

"Everything can be burned, of course," Kratish said. "If you apply enough energy, you can convert anything to carbon dioxide and water. But we wanted to find an elegant way to add the minimum amount of energy to derive the maximum value product."

Precision engineering

To uncover that elegant solution, Marks, Kratish and their team looked to hydrogenolysis, a process that uses hydrogen gas and a catalyst to break down polyolefin plastics into smaller, useful hydrocarbons. While hydrogenolysis approaches already exist, they typically require extremely high temperatures and expensive catalysts made from noble metals like platinum and palladium.

"The polyolefin production scale is huge, but the global noble metal reserves are very limited," Lai said. "We cannot use the entire metal supply for chemistry. And, even if we did, there still would not be enough to address the plastic problem. That's why we're interested in Earth-abundant metals."

For its polyolefin recycling catalyst, the Northwestern team pinpointed cationic nickel, which is synthesized from an abundant, inexpensive and commercially available nickel compound. While other nickel nanoparticle-based catalysts have multiple reaction sites, the team designed a single-site molecular catalyst.

The single-site design enables the catalyst to act like a highly specialized scalpel preferentially cutting carbon-carbon bonds rather than a less controlled blunt instrument that indiscriminately breaks down the plastic's entire structure. As a result, the catalyst allows for the selective breakdown of branched polyolefins (such as isotactic polypropylene) when they are mixed with unbranched polyolefins effectively separating them chemically.

"Compared to other nickel-based catalysts, our process uses a single-site catalyst that operates at a temperature 100 degrees lower and at half the hydrogen gas pressure," Kratish said. "We also use 10 times less catalyst loading, and our activity is 10 times greater. So, we are winning across all categories."

Accelerated by contamination

With its single, precisely defined and isolated active site, the nickel-based catalyst possesses unprecedented activity and stability. The catalyst is so thermally and chemically stable, in fact, that it maintains control even when exposed to contaminants like PVC. Used in pipes, flooring and medical devices, PVC is visually similar to other types of plastics but significantly less stable upon heating. Upon decomposition, PVC releases hydrogen chloride gas, a highly corrosive byproduct that typically deactivates catalysts and disrupts the recycling process.

Amazingly, not only did Northwestern's catalyst withstand PVC contamination, PVC actually accelerated its activity. Even when the total weight of the waste mixture is made up of 25% PVC, the scientists found their catalyst still worked with improved performance. This unexpected result suggests the team's method might overcome one of the biggest hurdles in mixed plastic recycling -- breaking down waste currently deemed "unrecyclable" due to PVC contamination. The catalyst also can be regenerated over multiple cycles through a simple treatment with inexpensive alkylaluminium.

"Adding PVC to a recycling mixture has always been forbidden," Kratish said. "But apparently, it makes our process even better. That is crazy. It's definitely not something anybody expected."

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Wednesday, September 24, 2025

Solar fuel conundrum in iron-based systems nears solution




Solar energy stored in the form of fuel is something scientists hope could partially replace fossil fuels in the future. Researchers at Lund University in Sweden may have solved a long-standing problem that has hindered the development of sustainable solar fuels. If solar energy can be used more efficiently using iron-based systems, this could pave the way for cheaper solar fuels.

"We can now see previously hidden mechanisms that would allow iron-based molecules to transfer charge more efficiently to acceptor molecules. This could effectively remove one of the biggest obstacles to producing solar fuels using common metals," says Petter Persson, a chemistry researcher at Lund University and an author of the study published in the Journal of the American Chemical Society.

An intense search for new ways to produce environmentally friendly fuels is underway. These could help phase out the fossil fuels that currently dominate global energy. One promising strategy is to develop catalysts that utilize solar energy to produce fuels such as green hydrogen.

In recent years, significant progress has been made in this area, including the development of solar-powered catalysts based on iron and other common elements. Despite these achievements, the conversion of energy from solar to fuel has proved too inefficient in iron-based systems.

To produce solar fuels such as green hydrogen, the light-absorbing molecules must transfer electrical charge to an acceptor molecule. If the transfer does not work well, much of the energy is lost before it can be stored in the solar fuel. Although iron is inexpensive and environmentally friendly, this problem has made it difficult to make iron-based systems work as efficiently as more expensive systems based on rare earth metals.

Using advanced calculations, the researchers have now been able to analyze the process at the molecular level. The study shows that much of the energy is lost because the acceptor molecules often stick to the catalysts before the charge has time to transfer.

However, the researchers discovered unexpected mechanisms whereby acceptor molecules can enlist the help of neighboring molecules to complete the charge transfer. This can significantly reduce energy losses and increase efficiency in iron-based solar energy systems.

"It was surprising that the surroundings play such a crucial role. Our simulations show several unexpected ways in which the interaction with neighboring molecules can facilitate the formation of energy-rich products," says Persson.

This is an important step towards viable solar fuel production with common metals. The study shows how the crucial first step of charge separation can be optimized, but further steps are necessary before the process can lead to finished solar fuels.

"The study provides new insights into how solar energy can be converted more efficiently using common metals such as iron. In the long run, this can contribute to the development of cheaper and more sustainable solar fuels an important piece of the puzzle in the global energy transition," concludes Persson.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Revolutionizing Chemistry: Trideuteromethylselenation! #sciencefather #A...

Tuesday, September 23, 2025

Enceladus’ ocean may not have produced precursor chemicals for life



Enceladus’ chilly geysers spew chemical compounds that hint at the potential for life in the moon of Saturn’s subsurface ocean.

But some compounds within the plumes may have formed via high-energy radiation above ground, a new study suggests. Researchers described the findings in a September 9 presentation at the Europlanet Science Congress–Division for Planetary Sciences of the American Astronomical Society joint meeting in Helsinki.

“We need to be careful when we’re thinking about Enceladus’ habitability, because it may not necessarily originate from the subsurface ocean,” says planetary scientist Grace Richards of the National Institute for Astrophysics in Rome.

When NASA’s Cassini spacecraft, which surveyed Saturn and its moons from 2004 to 2017, flew through plumes of ice and water sprayed from geysers near Enceladus’ south pole, the probe found organic compounds carbon-based building blocks of life. “What’s exciting about Enceladus is we have detected all the elements that we expect that we definitely need to find life,” Richards says.

Living things are thought to need liquid water, and the geysers provide a way to probe the ocean beneath the moon’s icy shell for signs of life or its precursors. But Richards wanted to determine whether some substances in and around the plumes originated from outside the ocean. Incoming radiation from Saturn’s surroundings could spark similar chemical reactions above ground.

Richards and colleagues created ices made of water, carbon dioxide, methane and ammonia at about –200° Celsius, the moon’s average surface temperature, and blasted them with charged particles. Afterward, the team heated the irradiated ices to around –100° C to mimic warmer spots on the moon, turning the ice to gas and exposing molecules trapped within.

The gas components and wavelengths of light absorbed by the ices revealed that the experiments produced some simple organic compounds, such as acetylene. Chemical reactions with these components can create complex molecules that could lead to life, Richards says.

Some of the lab-created molecules matched ones that were detected within Enceladus’ plumes, suggesting that these substances may not have come from the moon’s subsurface ocean after all. That doesn’t rule out the possibility of microbial life arising on Enceladus, Richards says. But researchers should take caution when interpreting molecules that could suggest life at least some may not be associated with biology.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Unlocking Aryl Radical Chemistry! #sciencefather #Analytical Chemistry# ...

Saturday, September 20, 2025

Nanoparticles Unveil Secrets of Ancient Ivories! #sciencefather #Analyti...

High-pressure hydride sees gold show its reactive side


Scientists at the European x-ray free-electron laser facility in Germany have created a solid gold hydride by compressing gold with hydrocarbons at pressures above 40GPa and heating it with ultrafast x-ray pulses above 2000K. The extreme conditions allow hydrogen atoms to occupy gaps in a hexagonal close-packed gold lattice, forming a compound that exists only at high temperatures and reverts to ordinary gold upon cooling.

This hydride forms near gold’s melting point. Computer simulations confirmed its structure, showing disordered hydrogen throughout the lattice and diffusing rapidly in a superionic fashion. The gold–hydrogen bonds have an unusually covalent nature for a metal–hydrogen interaction due to gold’s high electronegativity.




The compound is stable only at extreme temperatures, suggesting it forms through an entropy-driven reaction. On cooling, it reverts to ordinary face-centred cubic gold and molecular hydrogen. That explains why previous attempts to find gold hydrides had failed because the compound vanishes before it can be recovered under ambient conditions.

The discovery pushes chemists to rethink how chemically inert gold really is and raises questions about whether other ‘inert’ systems might have unexpected chemistry at extreme pressures and temperatures.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Friday, September 19, 2025

New Catalyst Could Make Plastic Recycling a Whole Lot Less Complicated




A new catalyst may enable mixed plastic recycling

The future of plastic recycling could soon become far simpler and more efficient.

Researchers at Northwestern University have developed a new plastic upcycling method that greatly reduces and may even eliminate the need to pre-sort mixed plastic waste.

At the heart of the process is a low-cost nickel-based catalyst that selectively targets polyolefin plastics, including polyethylenes and polypropylenes, which make up nearly two-thirds of global single-use plastic consumption. This means the catalyst could be applied to large volumes of unsorted polyolefin waste.

When activated, the catalyst converts these low-value solid plastics into liquid oils and waxes that can be repurposed into higher-value products such as fuels, lubricants, and candles. The catalyst can be reused multiple times and, notably, is also capable of breaking down plastics contaminated with polyvinyl chloride (PVC), a toxic material long considered to make plastics “unrecyclable.”

Key challenges and breakthrough potential

“One of the biggest hurdles in plastic recycling has always been the necessity of meticulously sorting plastic waste by type,” said Northwestern’s Tobin Marks, the study’s senior author. “Our new catalyst could bypass this costly and labor-intensive step for common polyolefin plastics, making recycling more efficient, practical, and economically viable than current strategies.”

“When people think of plastic, they likely are thinking about polyolefins,” said Northwestern’s Yosi Kratish, a co-corresponding author on the paper. “Basically, almost everything in your refrigerator is polyolefin-based squeeze bottles for condiments and salad dressings, milk jugs, plastic wrap, trash bags, disposable utensils, juice cartons and much more. These plastics have a very short lifetime, so they are mostly single-use. If we don’t have an efficient way to recycle them, then they end up in landfills and in the environment, where they linger for decades before degrading into harmful microplastics.”

A world-renowned catalysis expert, Marks is the Vladimir N. Ipatieff Professor of Catalytic Chemistry at Northwestern’s Weinberg College of Arts and Sciences and a professor of chemical and biological engineering at Northwestern’s McCormick School of Engineering. He is also a faculty affiliate at the Paula M. Trienens Institute for Sustainability and Energy. Kratish is a research assistant professor in Marks’ group, and an affiliated faculty member at the Trienens Institute. Qingheng Lai, a research associate in Marks’ group, is the study’s first author. Marks, Kratish and Lai co-led the study with Jeffrey Miller, a professor of chemical engineering at Purdue University; Michael Wasielewski, Clare Hamilton Hall Professor of Chemistry at Weinberg; and Takeshi Kobayashi a research scientist at Ames National Laboratory.

The polyolefin predicament

From yogurt cups and snack wrappers to shampoo bottles and medical masks, polyolefin plastics are part of everyday life. They are the most widely used plastics in the world, produced in enormous quantities. By some estimates, more than 220 million tons of polyolefin products are manufactured globally each year. Yet, according to a 2023 report in the journal Nature, recycling rates for these plastics remain troublingly low, falling between less than 1% and 10% worldwide.

This poor recycling record is largely due to the durability of polyolefins. Their structure is made up of small molecules connected by carbon-carbon bonds, which are notoriously strong and difficult to break apart.

“When we design catalysts, we target weak spots,” Kratish said. “But polyolefins don’t have any weak links. Every bond is incredibly strong and chemically unreactive.”

Problems with current processes

Currently, only a few, less-than-ideal processes exist that can recycle polyolefin. It can be shredded into flakes, which are then melted and downcycled to form low-quality plastic pellets. But because different types of plastics have different properties and melting points, the process requires workers to scrupulously separate various types of plastics. Even small amounts of other plastics, food residue, or non-plastic materials can compromise an entire batch. And those compromised batches go straight into the landfill.

Another option involves heating plastics to incredibly high temperatures, reaching 400 to 700 degrees Celsius. Although this process degrades polyolefin plastics into a useful mixture of gases and liquids, it’s extremely energy-intensive.

“Everything can be burned, of course,” Kratish said. “If you apply enough energy, you can convert anything to carbon dioxide and water. But we wanted to find an elegant way to add the minimum amount of energy to derive the maximum value product.”

Precision engineering

To uncover that elegant solution, Marks, Kratish, and their team looked to hydrogenolysis, a process that uses hydrogen gas and a catalyst to break down polyolefin plastics into smaller, useful hydrocarbons. While hydrogenolysis approaches already exist, they typically require extremely high temperatures and expensive catalysts made from noble metals like platinum and palladium.

“The polyolefin production scale is huge, but the global noble metal reserves are very limited,” Lai said. “We cannot use the entire metal supply for chemistry. And, even if we did, there still would not be enough to address the plastic problem. That’s why we’re interested in Earth-abundant metals.”

For its polyolefin recycling catalyst, the Northwestern team pinpointed cationic nickel, which is synthesized from an abundant, inexpensive, and commercially available nickel compound. While other nickel nanoparticle-based catalysts have multiple reaction sites, the team designed a single-site molecular catalyst.

The single-site design enables the catalyst to act like a highly specialized scalpel preferentially cutting carbon-carbon bonds rather than a less controlled blunt instrument that indiscriminately breaks down the plastic’s entire structure. As a result, the catalyst allows for the selective breakdown of branched polyolefins (such as isotactic polypropylene) when they are mixed with unbranched polyolefins effectively separating them chemically.

“Compared to other nickel-based catalysts, our process uses a single-site catalyst that operates at a temperature 100 degrees lower and at half the hydrogen gas pressure,” Kratish said. “We also use 10 times less catalyst loading, and our activity is 10 times greater. So, we are winning across all categories.”

Accelerated by contamination

With its single, precisely defined, and isolated active site, the nickel-based catalyst possesses unprecedented activity and stability. The catalyst is so thermally and chemically stable, in fact, that it maintains control even when exposed to contaminants like PVC. Used in pipes, flooring, and medical devices, PVC is visually similar to other types of plastics but significantly less stable upon heating. Upon decomposition, PVC releases hydrogen chloride gas, a highly corrosive byproduct that typically deactivates catalysts and disrupts the recycling process.

Amazingly, not only did Northwestern’s catalyst withstand PVC contamination, PVC actually accelerated its activity. Even when the total weight of the waste mixture is made up of 25% PVC, the scientists found their catalyst still worked with improved performance. This unexpected result suggests the team’s method might overcome one of the biggest hurdles in mixed plastic recycling breaking down waste currently deemed “unrecyclable” due to PVC contamination. The catalyst also can be regenerated over multiple cycles through a simple treatment with inexpensive alkylaluminium.

“Adding PVC to a recycling mixture has always been forbidden,” Kratish said. “But apparently, it makes our process even better. That is crazy. It’s definitely not something anybody expected.”

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Revolutionary Dual-Mode Biosensor Unveiled! #sciencefather #Analytical C...

Thursday, September 18, 2025

Scientists Grow “Gold Quantum Needles” for Sharper Biomedical Imaging




Potential applications range from biomedical imaging to the conversion of light energy.

University of Tokyo researchers Shinjiro Takano, Yuya Hamasaki, and Tatsuya Tsukuda have directly imaged how the geometric arrangement of atoms in gold nanoclusters develops at the very earliest stages of growth.

Under the same conditions, the team also “grew” an unexpected elongated nanocluster structure that they named “gold quantum needles.” Because these “needles” respond strongly to near-infrared light, they could enable much sharper biomedical imaging and more effective light-energy conversion. The findings were reported in the Journal of the American Chemical Society.

Gold may evoke luxury, yet at the nanoscale, it is a vital material in modern technology because it forms unusual structures with distinct properties. Gold nanoclusters with fewer than 100 atoms are typically produced by reducing, that is, adding electrons, gold precursor ions in the presence of protective ligands. Despite this, achieving precise control over size, shape, and composition remains difficult.

Opening the “Black Box” of Cluster Formation

“Over the past years,” says Tsukuda, the principal investigator, “much effort has been devoted to understanding the correlation between the structure and physicochemical properties of the nanoclusters. However, the formation process is regarded as a black box. We initiated this project with the belief that understanding the initial stages of cluster formation will lead to the development of new, targeted synthesis methods for desired structures.”

The researchers thus set out to determine the geometric structures of gold nanoclusters at the initial stages of their formation. They used slightly unusual synthesis conditions to trap the nanoclusters in the very first stages of growth. Single-crystal X-ray diffraction analysis, an X-ray for chemical compounds, if you will, revealed that gold nanoclusters grew anisotropically, at a different rate in different directions.

The Discovery of Gold Quantum Needles

Moreover, the analysis revealed an entirely new structure: pencil-shaped nanoclusters composed of triangular trimers and tetrahedral tetramers. The researchers named them “gold quantum needles” because the electrons confined in these nanoclusters demonstrated quantized behavior, a quantum phenomenon in which electrons can take only specific potential energies.

“We could retroactively explain the formation processes of a series of small gold nanoclusters under our unusual synthetic conditions,” Tsukuda explains. “However, the formation of needles with a base of a triangle of three gold atoms instead of a nearly spherical cluster is a serendipitous finding that was far beyond our imagination.”

The structural snapshots the researchers acquired of the stepwise growth of gold nanoclusters greatly contribute to our understanding of the formation mechanism. However, Tsukuda is already thinking about the next steps.

“We would like to explore synthesizing other, unique nanoclusters by refining the synthesis conditions further. We would also like to collaborate with other experts to promote the application of gold quantum needles, leveraging their exceptional optical properties.”

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Revolutionary Adhesives: The Future of Bonding! #sciencefather #Analytic...

Wednesday, September 17, 2025

Bimetallic Motors : Chemical Magnetism in Action! #sciencefather #Analyt...

Worse Than We Thought: “Forever Chemicals” Are Far More Acidic Than Previously Believed




New and more precise acidity measurements may help make PFAS easier to track.

Per- and polyfluoroalkyl substances (PFAS) are nicknamed “forever chemicals” in part because their acidity helps them linger in the environment.

Many of these toxic chemicals are strongly acidic, so they readily shed protons and take on a negative charge, which lets them dissolve in water and spread more easily.

New work shows some PFAS are even more acidic than earlier estimates a key piece of information for forecasting their movement through the environment and their potential effects on human health.

The study, led by the University at Buffalo, introduced a rigorous experimental approach to determine acidity for 10 PFAS types and three common breakdown products.

The lower the pKa, the more likely a chemical is to give up a proton and exist in its charged form.

“These findings suggest that previous measurements have underestimated PFAS’ acidity. This means their ability to persist and spread in the environment has been mischaracterized, too,” says the study’s corresponding author, Alexander Hoepker, PhD, a senior research scientist with the UB RENEW Institute.

More accurate pKa measurements help efforts to understand the behavior of PFAS in the environment. A chemical’s pKa could mean the difference as to whether it remains dissolved in water, sticks to soil or a biological membrane, or perhaps volatilizes into the air.

“If we’re going to understand how these concerning chemicals spread, it’s very important we have a reliable method for the accurate determination of their pKa values,” says Diana Aga, PhD, director of RENEW and SUNY Distinguished Professor and Henry M. Woodburn Chair in the UB Department of Chemistry.

Combining experiments with computations

PFAS are made of a highly fluorinated, water-repelling tail and a more water-loving headgroup. Many of the most scrutinized PFAS have a highly acidic headgroup, making them more likely to give up a proton and exist in its charged form.

Whether a PFAS exists in its neutral or charged form depends on the pH level of their surrounding environment. That’s where pKa comes in. It tells scientists the pH level at which a given PFAS is equal to flip from neutral to charged, or vice versa.

But there has been much disagreement about the pKa measurements of some PFAS, like PFOA, with different teams coming up with widely different values. One of the reasons for this may be the glass used during their experiments.

“PFAS likes to stick to glass. When that happens, it throws off traditional, so-called bulk measurements that quantify how much PFAS is in a solution,” Hoepker says. “In other cases, too much organic solvent is used to get PFAS into solution, which similarly biases the pKa measurement.”

To address this challenge, the UB team used fluorine and proton (hydrogen) nuclear magnetic resonance (NMR) spectroscopy think MRI for molecules. NMR places a sample in a strong magnetic field and probes its atomic nuclei with radio waves.

When a PFAS headgroup is negatively charged, nearby fluorine atoms respond at a different (radio) frequency.

Reading these atom-level signatures lets the researchers tell whether a PFAS molecule is charged or neutral capabilities that other methods that have been used previously cannot provide.

“This unique measurement allows NMR to inherently account for PFAS losses to glass or other adsorption behaviors, so your pKa measurements don’t end up way off the mark,” Hoepker says.

Some PFAS are so acidic (pKa of less than zero) that generating them in their neutral form would require super-acidic conditions (a pH level of less than zero) that are impractical in standard labs. In those cases, the research team paired NMR experiments with electronic-structure calculations using density functional theory to predict the NMR shifts of the neutral and ionized forms.

“We augmented partial NMR datasets with computational predictions to arrive at more accurate pKa values,” Hoepker says. “This NMR-centered hybrid approach integrating experimental measurements with computational analyses enhanced our confidence in the results and, to our knowledge, has not previously been applied to PFAS acidity.”

Problem PFAS measured more accurately

The PFAS that has been the most difficult to measure is PFOA, once commonly used in nonstick pans and deemed hazardous by the Environmental Protection Agency last year.

The team found its pKa to be –0.27, meaning it will be negatively charged at practically any realistic pH level. Previous experimental studies had measured its pKa as high as 3.8 and more commonly around 1, while the computational methods COSMO-RS and OPERA had determined its pKa at 0.24 and 0.34, respectively.

Trifluoroacetic acid (TFA) an emerging PFAS increasingly detected in waters worldwide and likely transported through the atmosphere and deposited by rain was found to be far more acidic than previously reported, with a pKa of around 0.03. Earlier estimates had anywhere from 0.30 to 1.1.

Notably, the team determined the pKa values for several prominent emerging PFAS that had never been measured, such as 5:3 fluorotelomer carboxylic acid (5:3 FTCA), and PFAS ethers like NFDHA and PFMPA that are newer PFAS but are also likely to pose challenges for regulators due to their health effects.

“This new experimental approach of determining pKa values for PFAS will have wide-ranging applications, from being able to validate computationally derived values, to facilitating the development of machine learning models that can better predict pKa values of newly discovered PFAS contaminants when reference standards are not available,” Aga says. “In turn, knowledge of the pKa values of emerging PFAS will allow researchers to develop appropriate analytical methods, remediation technologies, and risk assessment strategies more efficiently.”

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Tuesday, September 16, 2025

Chemists Create Next-Gen Rocket Fuel Compound That Packs 150% More Energy




UAlbany chemists created manganese diboride, a high-energy material with potential for rocket fuel and new technologies.

Chemists at the University at Albany have developed a high-energy compound that could transform rocket fuel and make space travel more efficient. When ignited, this compound produces significantly more energy per unit of weight and volume than current propellants.

For rockets, this means that less fuel would be needed to achieve the same mission duration or payload capacity, leaving more space for essential equipment and supplies. The research was published in the Journal of the American Chemical Society.

“In rocket ships, space is at a premium,” said Assistant Professor of Chemistry Michael Yeung, whose lab led the work. “Every inch must be packed efficiently, and everything onboard needs to be as light as possible. Creating more efficient fuel using our new compound would mean less space is needed for fuel storage, freeing up room for equipment, including instruments used for research. On the return voyage, this could mean more space is available to bring samples home.”

The compound, manganese diboride (MnB2), is more than 20% higher in energy density by weight and about 150% higher by volume compared with aluminum, which is currently used in solid rocket boosters. Despite its potency, it is remarkably stable and only ignites when exposed to an ignition source such as kerosene.

Beyond rocket propulsion, the boron-based structure of MnB2 shows wide-ranging potential. Work from the Yeung lab indicates it could also strengthen catalytic converters in automobiles and act as a catalyst for breaking down plastics.

It Takes Heat to Make Heat

Manganese diboride is part of a group of chemical compounds long suspected to have unusual properties, but progress in studying them has been limited by the challenge of actually producing the material.

“Diborides first started getting attention in the 1960s,” said UAlbany PhD student Joseph Doane, who works with Yeung. “Since these initial looks, new technologies are allowing us to actually synthesize chemical compounds that were once only hypothesized to exist.

“Knowing what we do about the elements on the periodic table, we suspected that manganese diboride would be structurally asymmetrical and unstable factors which together would make it highly energetic but until recently, we couldn’t test it because it couldn’t be made. Successfully synthesizing pure manganese diboride is an exciting achievement in and of itself. And now, we can test it experimentally and discover new ways to put it to use.”

Producing manganese diboride requires extreme heat, generated by a device known as an “arc melter.” To begin, manganese and boron powders are pressed into a pellet and sealed inside a reinforced glass chamber. A narrow electrical current is then directed at the pellet, heating it to nearly 3,000°C (over 5,000°F). The molten substance is rapidly cooled to preserve its structure. On the atomic scale, this process forces the central manganese atom to bond with more atoms than usual, creating a crowded arrangement tightly compressed like a coiled spring.

Unlocking the structure through deformation

When exploring new chemical compounds, being able to physically produce the compound is critical. You also need to be able to define its molecular structure in order to better understand why it behaves the way it does.

UAlbany PhD student Gregory John, who works with computational chemist Alan Chen, built computer models to visualize manganese diboride’s molecular structure. These models revealed something critical: a subtle skew, known as “deformation,” which gives the compound its high potential energy.

“Our model of the manganese diboride compound looks like a cross-section of an ice cream sandwich, where the outer cookies are made of a lattice structure comprised of interlocking hexagons,” said John. “When you look closely, you can see that the hexagons aren’t perfectly symmetrical; they’re all a little skewed. This is what we call ‘deformation.’ By measuring the degree of deformation, we can use that measure as a proxy to determine the amount of energy stored in the material. That skew is where the energy is stored.”

“Imagine a flat trampoline; there’s no energy there when it’s flat,” said Yeung. “If I put a gigantic weight in the center of the trampoline, it will stretch. That stretch represents energy being stored by the trampoline, which it will release when the object is removed. When our compound ignites, it’s like removing the weight from the trampoline and the energy is released.”

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Nanotech & AI: Revolutionizing Thermal Energy! #sciencefather #Analytica...

Friday, September 12, 2025

Nobelium becomes heaviest element with identified compounds

Nobelium is now the heaviest element to have been directly detected as part of a larger molecule. The new nobelium complexes were created as part of a series of investigations charting the chemistry on the edge of the actinide series.

Nobelium is element 102, and is too unstable to exist naturally on Earth. It was first made in particle accelerators in the 1950s, with Swedish, US and Russian teams all claiming to have been the first to have created it. As it has to be produced through nuclear reactions a single atom at a time, nobelium has remained one of the most mysterious elements on the periodic table, with no known uses and very few of its chemical properties confirmed experimentally.

In the new work, a team at Lawrence Berkeley National Laboratory in California, US, first created nobelium by firing a calcium beam into a lead target using a cyclotron particle accelerator, resulting in nuclear fusion. The team had then hoped to introduce the atom to water and nitrogen to form simple molecules, but soon found it had already happened. ‘We had a bit of a surprise,’ says physical chemist Jennifer Pore, who led the project. ‘We were producing nobelium molecules even before we tried. The nobelium ions were reacting with trace contaminants of nitrogen and water in our gases.’

The results, confirmed by a mass spectrometer, included a variety of nobelium complexes containing hydroxide, water and dinitrogen ligands. While compounds containing heavier elements have likely been made, the short-lived nature of the isotopes  usually measured in seconds  means that definitive confirmation is not possible, and instead relies indirect measurements. This new experiment means nobelium is now the heaviest element with a definitively identified compound.

The experiment is part of a wider programme of research by Pore that aims to investigate one of the periodic table’s most enduring mysteries: which end of the lanthanide and actinide series of elements belong in group 3? ‘You can learn a lot of interesting things about these molecules,’ Pore explains. ‘You can learn about preferred oxidation states, and that has a good tie-in to periodic table placement. But gas-phase chemistry can give you direct information about electronic orbitals, and how accessible electron configurations are.’ While nobelium fits the trend for the actinides as expected, Pore is now planning to investigate the next elements in sequence, including lawrencium (element 103), rutherfordium (element 104) and dubnium (element 105).

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Aryl Radical Chemistry! #sciencefather #Analytical Chemistry # chemistry...

Wednesday, September 10, 2025

Cracking the Code: Transthyretin Isolation! #sciencefather #Analytical C...

Chromatography and its importance


Chromatography is a laboratory technique used for separating the components of a mixture based on differences in how they interact with a stationary phase (e.g., a solid or gel) and a mobile phase (e.g., a liquid or gas).

Chromatography involves two key phases:

Stationary phase: Usually a solid or viscous liquid fixed in place (e.g., column material).


Mobile phase: A solvent that flows through the stationary phase, carrying the sample with it.

As the sample moves with the mobile phase, its components interact differently with the stationary phase, causing them to separate.

🌟 Importance of Chromatography

Purity – Essential for purifying compounds in pharmaceuticals and research.

Identification – Helps identify unknown substances in complex mixtures.

Quantification – Measures the amount of specific components in a sample.

Diagnosis – Used in medical diagnostics to analyze blood, urine, etc.

Research – Crucial for studying proteins, DNA, metabolites, and chemicals.

Uses of Chromatography

Chromatography has a wide range of applications across multiple disciplines. In pharmaceuticals, it’s used to ensure the safety and efficacy of drugs by analyzing their components. In biotechnology, chromatography is employed to purify proteins like insulin or antibodies from complex mixtures. Environmental scientists use it to detect harmful pollutants in air, water, and soil. In the food industry, it identifies additives, preservatives, and any harmful contaminants. Forensic experts rely on it for toxicology reports and to analyze samples from crime scenes. Clinical laboratories use it for diagnostic tests by analyzing blood or urine to detect specific biomarkers or disease indicators. Each of these uses highlights the versatility and necessity of chromatography in modern science and industry.

Types of Chromatography

There are several types of chromatography, each suited for specific applications:

Column Chromatography involves passing a mixture through a column packed with a stationary phase. It is commonly used in laboratories to separate and purify individual chemical compounds, especially proteins and enzymes.

Gas Chromatography (GC)
uses an inert gas as the mobile phase and is ideal for separating volatile substances. It is widely used in forensic science, environmental analysis, and testing for drug residues.

Liquid Chromatography (LC), especially High-Performance Liquid Chromatography (HPLC), uses a liquid mobile phase under high pressure. It is a standard method in pharmaceutical and biochemical labs for analyzing complex mixtures with high precision.

Thin-Layer Chromatography (TLC) is a simple and cost-effective method where a sample moves across a coated glass or plastic plate. It’s often used for quick checks of compound identity or reaction progress.

Affinity Chromatography utilizes specific interactions between molecules, such as antigen-antibody or enzyme-substrate binding. This method is highly selective and is particularly useful in purifying biomolecules like antibodies or hormones.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Tuesday, September 9, 2025

Researchers Crack One of Aromatic Chemistry’s Toughest Challenges




The method has applications in organic chemistry, particularly within the pharmaceutical industry.

A team of scientists has developed an electrochemical technique that enables precise, para-position single-carbon insertion into polysubstituted pyrroles. This advancement holds significant promise for synthetic organic chemistry, particularly in the development of pharmaceutical compounds.

“We set out to address the longstanding challenge of achieving single-carbon insertion into aromatic rings with precise positional control,” said Mahito Atobe, Professor, Faculty of Engineering, Yokohama National University.

Chemical transformations that alter aromatic rings are fundamental to creating pharmaceuticals and advanced materials. However, introducing a single carbon atom at a specific site, especially at the para position, has been extremely difficult to achieve. The para position refers to the specific arrangement of atoms in a molecule, where substituents (atoms that replace a hydrogen atom) are located opposite each other on an aromatic ring.

In this method, a single carbon atom is added directly into the molecular framework. This can extend a carbon chain or increase the size of a ring structure by one carbon atom, offering a powerful new tool for molecular design.

Introducing a Novel Electrochemical Strategy

“Our goal was to develop a new, electrochemically driven method that enables this transformation selectively and efficiently, while gaining mechanistic insights into how the electronic structure of the substrate controls the insertion position,” said Atobe. This study presents a novel concept for single-carbon insertion chemistry and expands a researcher’s chemical toolbox for synthesizing polysubstituted (hetero)aromatic compounds. Polysubstituted pyrroles are organic compounds that have a pyrrole ring and multiple substituents are joined to it. These compounds play a crucial role in diverse fields, such as natural products, pharmaceuticals, and functional materials. They hold particular interest for pharmaceuticals, where they are fundamental to many approved drugs.

“We discovered an electrochemical method that enables highly selective para-position single-carbon insertion into polysubstituted pyrroles an unprecedented transformation,” said Naoki Shida, Associate Professor, Faculty of Engineering, Yokohama National University. This reaction is enabled with distonic radical cation intermediates and is governed by the electronic properties of nitrogen-protecting groups. “Our findings establish a new strategy for site-selective molecular editing of aromatic rings, expanding the toolkit for synthetic organic chemistry,” said Shida.

Mechanism and Proof of Concept

The team demonstrated the electrochemical ring expansion reaction using α-H diazo esters as a carbynyl anion equivalent. This approach allowed efficient single-carbon insertion into a range of polysubstituted pyrroles, affording structurally diverse pyridine derivatives. They controlled the insertion position through electronic perturbation by the N-protecting group (PG), and achieved unprecedented para-selective insertion by introducing an electron-withdrawing protecting group to the pyrrole derivatives.

The team used in-situ spectroscopy and theoretical calculations to support the reaction mechanism involving a distonic radical cation intermediate. The spectroscopy and calculations suggest distonic radical cation intermediates are involved, facilitating carbon-atom migration on the aromatic ring and enabling insertion at different positions.

Approved drugs like Netupitant, Esomeprazole, Pyridoxine, and Opicapone contain benzene and pyridine rings with more than three substituents. These drugs are important medications for wide-ranging health challenges, such as Parkinson’s disease, stomach ulcers, or the control of chemotherapy-induced nausea. To synthesize these compounds, researchers have used multiple methods, such as coupling reactions, carbon-hydrogen functionalization, and cyclization reactions.

Single-carbon insertion is yet another approach scientists have used to modify polysubstituted (hetero)aromatic compounds. The single-carbon insertion approach significantly alters the structure of the parent skeletons. But up to this point in time, controlling the insertion position had been a significant challenge for researchers. The team’s novel electrochemical method introduces a new concept for single-carbon insertion chemistry.

Looking to the Future

Looking ahead, the team’s next step is to expand the scope of this reaction to a broader range of heteroaromatic compounds and complex molecules, including pharmaceutical intermediates.

“We also aim to integrate this methodology into flow electrolysis systems to improve scalability and efficiency. Ultimately, our goal is to establish a general platform for precise molecular editing of aromatic frameworks using electricity as a clean and controllable driving force,” said Atobe.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Water's Magic on Arylazo Sulfonates! #sciencefather #Analytical Chemistr...

Monday, September 8, 2025

Scientists Use Lightning To Make Ammonia out of Thin Air




A lightning-inspired process creates ammonia from air. The approach may support future green energy solutions.

Researchers at the University of Sydney have used artificial lightning to create a more efficient technique for producing ammonia, a chemical essential to modern life. Ammonia plays a key role in fertilizers that contribute to nearly half of global food production.

The team developed a simplified process to produce ammonia (NH₃) directly in its gaseous form. In contrast, earlier methods developed by other labs yielded ammonium (NH₄⁺) in solution, which demands additional energy and conversion steps to obtain usable ammonia gas.

Traditionally, ammonia is produced using the Haber-Bosch process, a method with a substantial environmental impact due to its high carbon emissions. This approach also requires large-scale infrastructure and proximity to inexpensive natural gas sources to remain economically viable.

The chemical process that fed the world, and the Sydney team looking to revolutionize it

Ammonia was once so highly valued primarily in the form of bird droppings that it became a source of conflict.

The development of the Haber-Bosch process in the 19th century enabled the large-scale production of synthetic ammonia, transforming both agriculture and industry. Today, approximately 90 percent of the world’s ammonia is still produced using this method.

“Industry’s appetite for ammonia is only growing. For the past decade, the global scientific community, including our lab, wants to uncover a more sustainable way to produce ammonia that doesn’t rely on fossil fuels.

“Currently, generating ammonia requires centralized production and long-distance transportation of the product. We need a low-cost, decentralized and scalable ‘green ammonia’,” said lead researcher Professor PJ Cullen from the University of Sydney’s School of Chemical and Biomolecular Engineering and the Net Zero Institute. His team has been working on ‘green ammonia’ production for six years.

“In this research, we’ve successfully developed a method that allows air to be converted to ammonia in its gaseous form using electricity. A huge step towards our goals.”

Ammonia is composed of three hydrogen atoms, making it a promising carrier and source of hydrogen for energy applications. It also offers potential for storing and transporting hydrogen, as the hydrogen can be extracted by a process known as “cracking,” which separates the molecules.

Because of its chemical properties, ammonia is being explored as a carbon-free fuel alternative. This has drawn attention from the shipping sector, which contributes roughly 3 percent of global greenhouse gas emissions.

Cracking a chemical conundrum

Professor Cullen’s team’s new method to generate ammonia works by harnessing the power of plasma, by electrifying or exciting the air.

But the star is a membrane-based electrolyzer, a seemingly non-descript silver box, where the conversion to gaseous ammonia happens.

During the Haber-Bosch process, ammonia (NH3) is made by combining nitrogen (N2) and hydrogen (H2) gases under high temperatures and pressure in the presence of a catalyst (a substance that speeds up a chemical reaction).

The plasma-based method Professor Cullen’s team developed uses electricity to excite nitrogen and oxygen molecules in the air. The team then passes these excited molecules to the membrane-based electrolyser to convert the excited molecules to ammonia.

The researchers said this is a more straightforward pathway for ammonia production.

Professor Cullen said the findings signal a new phase in making green ammonia possible. The team is now working on making the method more energy efficient and competitive compared to the Haber-Bosch process.

“This new approach is a two-step process, namely combining plasma and electrolysis. We have already made the plasma component viable in terms of energy efficiency and scalability.

“To create a more complete solution to a sustainable ammonia productive, we need to push the energy efficiency of the electrolyser component,” Professor Cullen said.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Revolutionary Dual-Mode Biosensor Unveiled! #sciencefather #Analytical C...

Saturday, September 6, 2025

Green Chemistry:Sustainable Analysis! #sciencefather #Analytical Chemist...

New Catalyst Breakthrough Slashes Platinum Use in Green Hydrogen Tech




Researchers engineered a graphene-encased catalyst with ultra-low platinum use that delivers high-efficiency, industrial-scale hydrogen production.

Proton exchange membrane (PEM) water electrolysis plays a key role in the production of green hydrogen on a large scale. One of the most commonly used materials in this process is Platinum on Carbon (Pt/C), which serves as an advanced cathode catalyst. Its popularity comes from its ability to effectively bind hydrogen and its strong resistance to acidic environments. However, using high amounts of platinum makes this approach expensive and limits its broader adoption.

Their innovation centers around a unique “chainmail” catalyst made from a cobalt-nickel (CoNi) nano-alloy that is enclosed within a single layer of graphene. The team found that electrons transferred from the CoNi alloy into the surrounding carbon layer. This process, combined with a 3d-2p electronic interaction, caused the surface of the graphene to accumulate an uneven distribution of Ï€ electronic states, which played a critical role in enhancing catalytic behavior.
Synergistic Confinement and Platinum Stability

After depositing Pt single atoms using atomic layer deposition, these enriched asymmetric π electrons exhibited a unique confinement effect on the Pt atoms.

This confinement operated through two synergistic mechanisms. Electron transfer from CoNi to Pt via the graphene layer resulted in an electron-rich Pt site, optimizing hydrogen adsorption energy and promoting hydrogen desorption, thereby improving catalytic activity. Besides, strong interactions between the asymmetric π electrons and the Pt 5d orbital enhanced the structural stability of Pt sites, boosting the durability of the catalyst.

The researchers assembled a PEM water electrolyzer using this catalyst, which achieved an ultra-high current density of 4.0 A cm−2 at 2.02 V and maintained excellent durability over 1,000 hours at 2 A cm−2, using only 1.2 μgPt cm−2 Pt loading. They also assembled a 2.85 kW PEM water electrolyzer using this catalyst, which operated stably for over 300 hours at an industrial current density of 1.5 A cm−2, highlighting its outstanding industrial application potential.

“This work provides a new idea for developing high-performance, long-life, and low-cost catalysts for hydrogen production via acid water electrolysis,” said Prof. Deng.

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com

Thursday, September 4, 2025

Rewriting Chemical Rules: Researchers Accidentally Create Unprecedented New Gold Compound




SLAC scientists created gold hydride in extreme lab conditions. The work sheds light on dense hydrogen and fusion processes.

By chance and for the first time, an international team of researchers led by scientists at the U.S. Department of Energy’s SLAC National Accelerator Laboratory succeeded in creating solid binary gold hydride a compound composed solely of gold and hydrogen atoms.

The team had originally set out to investigate how hydrocarbons, molecules made of carbon and hydrogen, transform into diamonds under extreme pressure and heat. During experiments at the European XFEL (X-ray Free-Electron Laser) in Germany, they placed hydrocarbon samples with a thin layer of gold foil, intended only to absorb X-rays and transfer heat to the relatively weakly absorbing hydrocarbons. Unexpectedly, alongside diamond formation, they observed the creation of gold hydride.

“It was unexpected because gold is typically chemically very boring and unreactive – that’s why we use it as an X-ray absorber in these experiments,” explained Mungo Frost, a staff scientist at SLAC and the study’s lead author. “These results suggest there’s potentially a lot of new chemistry to be discovered at extreme conditions where the effects of temperature and pressure start competing with conventional chemistry, and you can form these exotic compounds.”

The findings, published in Angewandte Chemie International Edition, demonstrate how chemical behavior can shift dramatically under extreme environments, such as those found deep inside planets or within hydrogen-fusing stars.

Studying dense hydrogen

To achieve these results, the researchers compressed hydrocarbon samples to pressures exceeding those inside Earth’s mantle using a diamond anvil cell. They then exposed the samples to bursts of X-ray pulses from the European XFEL, heating them above 3,500 degrees Fahrenheit. By analyzing how the X-rays scattered from the samples, the team tracked the structural changes taking place.

As anticipated, the data confirmed that carbon atoms had arranged into a diamond lattice. However, they also revealed unexpected signals: hydrogen atoms had reacted with the gold foil to form gold hydride.

At the conditions generated in the experiment, hydrogen existed in a dense, “superionic” state, in which hydrogen atoms moved freely within the rigid gold lattice. This behavior enhanced the conductivity of the gold hydride, offering new insight into the behavior of materials under extreme pressures and temperatures.

Hydrogen, which is the lightest element of the periodic table, is tricky to study with X-rays because it scatters X-rays only weakly. Here, however, the superionic hydrogen interacted with the much heavier gold atoms, and the team was able to observe hydrogen’s impact on how the gold lattice scattered X-rays. “We can use the gold lattice as a witness for what the hydrogen is doing,” Mungo said.

The gold hydride offers a way to study dense atomic hydrogen under conditions that might also apply to other situations that are experimentally not directly accessible. For example, dense hydrogen makes up the interiors of certain planets, so studying it in the lab could teach us more about those foreign worlds. It could also provide new insights into nuclear fusion processes inside stars like our sun and help develop technology to harness fusion energy here on Earth.

Exploring new chemistry

In addition to paving the way for studies of dense hydrogen, the research also offers an avenue for exploring new chemistry. Gold, which is commonly regarded as an unreactive metal, was found to form a stable hydride at extremely high pressure and temperature. In fact, it appears to be only stable at those extreme conditions as when it cools down, the gold and hydrogen separate. The simulations also showed that more hydrogen could fit in the gold lattice at higher pressure.

The simulation framework could also be extended beyond gold hydride. “It’s important that we can experimentally produce and model these states under these extreme conditions,” said Siegfried Glenzer, High Energy Density Division director and professor for photon science at SLAC and the study’s principal investigator. “These simulation tools could be applied to model other exotic material properties in extreme conditions.”

#AnalyticalChemistry, #ScienceOfSolutions, #ChemicalAnalysis, #Spectroscopy, #Chromatography, #LabScience, #PrecisionMatters, #ScienceInEveryDrop, #ChemistryMatters, #InnovationThroughAnalysis

For More Details

🌎Visit Our Website : analyticalchemistry.org

✉️Contact Us: mail@analyticalchemistry.org

Get Connected Here:
=====================
Twitter : x.com/ChemistryAwards
Facebook : www.facebook.com/profile.php?id=61566931868357
Pinterest : in.pinterest.com/analyticalchemistry25
Blog : analyticalchemistryawards.blogspot.com