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Chemistry

Breaking Down Barriers in Chemical Reactions: Oregon State University Researchers Revolutionize Hydrogenation Process

A chemical reaction that’s vital to a range of commercial and industrial goods may soon be initiated more effectively and less expensively.

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Breaking Down Barriers in Chemical Reactions: Oregon State University Researchers Revolutionize Hydrogenation Process

Chemical reactions are the backbone of various industries, from food production to fuel refining. However, many of these processes rely on expensive and inefficient catalysts that hinder their economic viability. Researchers at Oregon State University College of Engineering have joined forces with international collaborators to tackle this challenge by investigating single-atom catalysts (SACs), a relatively new class of catalysts that shows immense potential.

According to Zhenxing Feng, an associate professor of chemical engineering, hydrogenation – the process of adding diatomic hydrogen molecules to other compounds – is a critical and diverse reaction used in the creation of food products, fuels, commodity chemicals, and pharmaceuticals. However, this process requires expensive catalysts like palladium or platinum to increase its reaction rate and lower costs.

Feng and his team took a deep dive into SACs, which are catalysts where metal catalytic sites exist as isolated single atoms on a supporting substrate. They collaborated with researchers from four institutions in China to create and characterize 34 palladium SACs on 14 semiconductor supports.

The advanced X-ray, infrared, and electrochemical characterization techniques used by the team revealed that the effectiveness of SACs depended on how well a substrate could accept electrons. This connection was consistent and predictable, showing that the catalytic abilities of palladium SACs have a universal linear relationship with the molecular orbital position of their supporting substrates.

This groundbreaking discovery opens up new avenues for screening metal-support pairs for high activity and stability. The researchers also found that the molecular orbital position can be tuned by reducing support particle size, leading to SACs with record-high activities and excellent stabilities.

The team tested this newfound understanding on the semihydrogenation of acetylene in excess ethylene, a common industrial process used to convert vegetable oils into margarine and shortening. Their results demonstrated that SACs can be used more effectively and less expensively than traditional catalysts, making this breakthrough a significant step towards improving various commercial processes.

This study was funded by the OSU China Experience Fund, the National Natural Science Foundation of China Center for Single-Atom Catalysis, and other international collaborators, including researchers from the National University of Defense Technology and Suzhou Laboratory. The findings have been published in Nature and mark a major milestone in the field of chemical engineering research.

Chemistry

Revolutionizing Magnetic Field Technology: A Breakthrough Design for MRI and Magnetic Levitation

Two German physicists have reimagined how to create powerful and uniform magnetic fields using compact permanent magnets. By overcoming the limitations of the well-known Halbach array, which works only with infinitely long magnets, they engineered innovative 3D magnet arrangements that work in practical, finite-size setups. Their designs not only boost field strength but also enhance homogeneity, verified through real-world experiments. This game-changing advancement could help bring affordable MRI technology to underserved regions and power applications like particle accelerators and magnetic levitation systems.

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Physicists at the University of Bayreuth and Johannes Gutenberg University Mainz have made a groundbreaking discovery that could transform the way we generate magnetic fields. Prof. Dr. Ingo Rehberg and Dr. Peter Blümler developed an innovative approach to create homogeneous magnetic fields using compact, permanent magnets. This breakthrough design outperforms the traditional Halbach arrangement, which is ideal only for infinitely long and therefore unrealizable magnets.

The new approach presents optimal three-dimensional arrangements of very compact magnets, idealized by point dipoles. The researchers investigated the optimal orientation of the magnets for two geometries relevant to practical use: a single ring and a stacked double ring. This “focused” design allows the generation of homogeneous fields outside the magnet plane, enabling applications such as magnetic levitation systems.

To validate their theoretical predictions, Rehberg and Blümler constructed magnet arrays from 16 FeNdB cuboids mounted on 3D-printed supports. The resulting magnetic fields were measured and compared with theoretical calculations, revealing excellent agreement. In terms of both magnetic field strength and homogeneity, the new configurations clearly outperform the classical Halbach arrangement.

The potential applications of this breakthrough design are vast. Conventional MRI technology relies on powerful superconducting magnets, which are technically complex and extremely costly. The new approach offers a promising alternative for generating homogeneous magnetic fields using permanent magnets. Additionally, this innovation could lead to advancements in particle accelerators and magnetic levitation systems.

This study was published in the renowned interdisciplinary journal Physical Review Applied, showcasing significant advances at the intersection of physics with engineering, materials science, chemistry, biology, and medicine. The implications of this breakthrough design are far-reaching, and further research is expected to uncover new possibilities for its applications.

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Chemistry

Breakthrough at Rice University Keeps CO2 Electrolyzers Running 50x Longer with a Surprisingly Simple Method

A Rice University team discovered that bubbling CO₂ through a mild acid dramatically improves the lifespan and efficiency of electrochemical devices that convert CO₂ into useful fuels. This simple trick prevents salt buildup—a major barrier to commercialization—by altering local chemistry just enough to keep salts dissolved and flowing. The result? A device that ran for over 4,500 hours without clogging, using common catalysts and scalable technology. It’s a breakthrough that could make green CO₂ conversion far more viable in the real world.

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The researchers at Rice University have made a groundbreaking discovery that vastly improves the stability of electrochemical devices converting carbon dioxide into useful fuels and chemicals. Their innovative approach involves simply sending the CO2 through an acid bubbler, which dramatically extends the operational life of these devices by more than 50 times.

Electrochemical CO2 reduction (CO2RR) is a promising green technology that uses electricity to transform climate-warming CO2 into valuable products like carbon monoxide, ethylene, or alcohols. These products can be further refined into fuels or used in industrial processes, potentially turning a major pollutant into a feedstock.

However, the practical implementation of this technology has been hindered by poor system stability due to salt buildup in gas flow channels. This issue occurs when potassium ions migrate from the anolyte across the anion exchange membrane to the cathode reaction zone and combine with CO2 under high pH conditions.

To combat this problem, the Rice team tried a clever twist on standard procedures. Instead of using water to humidify the CO2 gas input into the reactor, they bubbled the gas through an acid solution such as hydrochloric, formic, or acetic acid.

The vapor from the acid altered local chemistry in trace amounts, preventing salt crystallization and channel blockage. The effect was remarkable: systems operated stably for over 4,500 hours in a scaled-up electrolyzer, compared to just about 80 hours under standard water-humidified CO2 conditions.

This breakthrough has significant implications for the development of carbon capture and utilization technologies. By extending the lifespan of CO2 electrolyzers, this innovation can help make these technologies more commercially viable and sustainable.

The simplicity of this approach is noteworthy, as it requires only small tweaks to existing humidification setups, which means it can be adopted without significant redesigns or added costs. This makes it an attractive solution for industries looking to integrate carbon utilization technologies into their operations.

This work was supported by the Robert A. Welch Foundation, Rice University, the National Science Foundation, and the David and Lucile Packard Foundation. The researchers’ findings have the potential to transform the field of CO2RR and pave the way for more durable, scalable electrochemical devices that can efficiently convert CO2 into valuable products.

The study’s authors highlight the significance of this discovery, saying it “addresses a long-standing obstacle with a low-cost, easily implementable solution.” They also emphasize its potential impact on making carbon utilization technologies more commercially viable and sustainable.

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Chemistry

“Rewriting Chemistry with Light: A Breakthrough in Fossil Fuel Transformation”

Researchers at Colorado State University have developed a new photoredox catalysis system that uses visible light mimicking photosynthesis to drive energy-intensive chemical reactions at room temperature. This groundbreaking process could significantly reduce the energy required in chemical manufacturing, especially in industries reliant on fossil fuels.

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The world is on the cusp of a revolutionary change in the way we transform fossil fuels into useful modern chemicals. Researchers at Colorado State University have made a groundbreaking discovery that uses light to rewrite the chemistry of fossil fuels, reducing energy demands and associated pollution. This breakthrough, published in Science, could be a game-changer for industries reliant on chemical manufacturing.

At the forefront of this research are professors Garret Miyake and Robert Paton from the Department of Chemistry and the Center for Sustainable Photoredox Catalysis (SuPRCat). Inspired by photosynthesis, their organic photoredox catalysis system harnesses visible light to gently alter the properties of chemical compounds. By exposing them to two separate photons, the team’s system generates energy needed for desired reactions, performing super-reducing reactions that are normally difficult and energy-intensive.

The research has shown remarkable results on aromatic hydrocarbons – resistant compounds like benzene in fossil fuels. Miyake boasts that their technology is “the most efficient system currently available” for reducing these compounds, paving the way for the production of chemicals needed for plastics and medicine.

This work continues the efforts of the U.S. National Science Foundation Center for Sustainable Photoredox Catalysis at CSU, led by Miyake as its director. This multi-institution research effort aims to transform chemical synthesis processes across various uses, making synthetic and computational chemists team up to understand the fundamental chemical nature of photoredox catalysis.

Katharine Covert, program director for the NSF Centers for Chemical Innovation program, highlights the importance of photoredox catalysis in pharmaceutical development and other industries. Through the NSF Center for Sustainable Photoredox Catalysis, researchers are developing catalysis systems similar to the one described in this paper to support energy-efficient production of ammonia for fertilizers, the breakdown of PFAS forever chemicals, and the upcycling of plastics.

Miyake emphasizes the urgency of meeting these challenges and making a more sustainable future for our world. He concludes that “the world has a timeclock that is expiring,” and we must develop sustainable technologies before it’s too late.

This breakthrough has far-reaching implications, not just in chemical manufacturing but also in addressing pressing environmental concerns. As researchers continue to push the boundaries of what’s possible with light-based chemistry, one thing is certain – the future of fossil fuel transformation has never looked brighter.

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