Lifeboat Foundation

To make long-term presence on the Moon viable, we need abundant electrical power. We can make power systems on the Moon directly from materials that exist everywhere on the surface, without special substances brought from Earth. We have pioneered the technology and demonstrated all the steps. Our approach, Blue Alchemist, can scale indefinitely, eliminating power as a constraint anywhere on the Moon.

We start by making regolith simulants that are chemically and mineralogically equivalent to lunar regolith, accounting for representative lunar variability in grain size and bulk chemistry. This ensures our starting material is as realistic as possible, and not just a mixture of lunar-relevant oxides. We have developed and qualified an efficient, scalable, and contactless process for melting and moving molten regolith that is robust to natural variations in regolith properties on the Moon.

Using regolith simulants, our reactor produces iron, silicon, and aluminum through molten regolith electrolysis, in which an electrical current separates those elements from the oxygen to which they are bound. Oxygen for propulsion and life support is a byproduct.

A new chemical process developed by Danish company Vestas can ensure that wind turbine blades are recycled at the end of their life, instead of being abandoned or going to landfill sites.

Wind power is one of the best ways to decarbonise the world’s electricity. Recent years have seen explosive growth in capacity additions, as well as gigantic new turbine designs able to generate as much as 18 MW. The costs keep falling, while efficiencies continue to improve. The trend is now obvious: renewable energy is the future and will inevitably displace fossil fuels.

Artificial intelligence and machine learning have made tremendous progress in the past few years including the recent launch of ChatGPT and art generators, but one thing that is still outstanding is an energy-efficient way to generate and store long-and short-term memories at a form factor that is comparable to a human brain. A team of researchers in the McKelvey School of Engineering at Washington University in St. Louis has developed an energy-efficient way to consolidate long-term memories on a tiny chip.

Shantanu Chakrabartty, the Clifford W. Murphy Professor in the Preston M. Green Department of Electrical & Systems Engineering, and members of his lab developed a relatively simple device that mimics the dynamics of the brain’s synapses, connections between neurons that allows signals to pass information. The artificial synapses used in many modern AI systems are relatively simple, whereas biological synapses can potentially store complex memories due to an exquisite interplay between different chemical pathways.

Chakrabartty’s group showed that their artificial synapse could also mimic some of these dynamics that can allow AI systems to continuously learn new tasks without forgetting how to perform old tasks. Results of the research were published Jan. 13 in Frontiers in Neuroscience.

Is Director of the Division of Research, Innovation and Ventures (DRIVe — https://drive.hhs.gov/) at the Biomedical Advanced Research and Development Authority (https://aspr.hhs.gov/AboutASPR/ProgramOffices/BARDA/Pages/default.aspx), a U.S. Department of Health and Human Services (HHS) office responsible for the procurement and development of medical countermeasures, principally against bioterrorism, including chemical, biological, radiological and nuclear (CBRN) threats, as well as pandemic influenza and emerging diseases.

Dr. Patel is committed to advancing high-impact science, building new products, and launching collaborative programs and initiatives with public and private organizations to advance human health and wellness. As the DRIVe Director, Dr. Patel leads a dynamic team built to tackle complex national health security threats by rapidly developing and deploying innovative technologies and approaches that draw from a broad range of disciplines.

Continue reading “Dr. Sandeep Patel, Ph.D. — BARDA — Developing Effective Life-Saving Medical Countermeasures For All” »

“Every act of creation,” Picasso famously noted, “is first an act of destruction.”

Taking this concept literally, researchers in Canada have now discovered that “breaking” molecular nanomachines basic to life can create new ones that work even better.

Their findings are published today in Nature Chemistry.

Scientists have found a clever way to generate hydrogen straight from salty seawater. This could be another step towards a clean energy future, if renewables power the process.

The new device makes a few chemical modifications to existing technologies, making it possible to extract hydrogen from untreated, unpurified seawater – which could alleviate concerns about using precious water supplies.

“We have split natural seawater into oxygen and hydrogen… to produce green hydrogen by electrolysis, using a non-precious and cheap catalyst in a commercial electrolyzer,” explains chemical engineer Shizhang Qiao of the University of Adelaide in Australia.

With a big assist from artificial intelligence and a heavy dose of human touch, Tim Cernak’s lab at the University of Michigan has made a discovery that dramatically speeds up the time-consuming chemical process of building molecules that will be tomorrow’s medicines, agrichemicals or materials.

The discovery, published in the Feb. 3 issue of Science, is the culmination of years of chemical synthesis and data science research by the Cernak Lab in the College of Pharmacy and Department of Chemistry.

The goal of the research was to identify key reactions in the synthesis of a molecule, ultimately reducing the process to as few steps as possible. In the end, Cernak and his team achieved the synthesis of a complex alkaloid found in nature in just three steps. Previous syntheses had taken between seven and 26 steps.

Claudiu Stan of Rutgers University—Newark, New Jersey, and his colleagues were watching moving drops of supercooled water spontaneously freeze when they noticed something unexpected: drops kept suddenly disappearing. Initially they thought that the lost drops had shattered as they froze. But, on closer inspection, they found that the icy drops were still there, they had just moved out of view. The team has now developed a quantitative model for this behavior, attributing it to a rocket-like propulsion mechanism induced by the freezing process [1]. Stan says that the finding could inspire scientists to design self-propelled systems powered by such phase transitions.

The team’s results add to a growing body of work on self-propelled drops. The mechanisms behind such motion vary wildly, but Stan notes that they all involve symmetry breaking. For the freezing drops, this symmetry breaking arises when the ice nucleation starts off-center. When ice nucleates, the change in structure releases latent heat, causing the local evaporation rate to suddenly increase, and if the nucleation is off-center, this enhanced evaporation occurs unevenly over the drop’s surface. Like a rocket ejecting a propellant heated by a chemical reaction, this asymmetrical evaporation increases the drop’s momentum, with the team’s model predicting peak velocities of nearly 1 m/s.

Stan says that this propulsion mechanism has a unique feature that could make it attractive for applications: unlike most self-propelled particles, it requires no surfaces and no surrounding fluid (the experiments were done under vacuum). But, for him, the findings have another bonus: “I am a fan of space exploration, so it was exciting to realize that [we could] draw an analogy between these tiny droplets and rockets,” he says.

In recent years, organic chemicals containing boron (B) and silicon (Si) have found applications in various fields, including optoelectronics and pharmaceuticals. Moreover, they can also serve as building blocks for complex organic chemicals. As a result, scientists are actively looking for new ways to leverage these versatile chemical tools as well as produce more kinds of organosilicon and organoboron compounds.

One limitation of the synthesis methods currently available for these chemicals is that we cannot introduce multiple B-and Si-containing groups in aromatic nitrogen heterocycles, i.e., carbon rings in which one of the carbon atoms is replaced by a nitrogen atom. If we could produce and freely transform such molecules, it would unlock the synthesis of several compounds relevant in medicinal chemistry.

Fortunately, a research team including Assistant Professor Yuki Nagashima from Tokyo Institute of Technology (Tokyo Tech), Japan has found a straightforward way around this limitation. As explained in their most recent study published in Nature Communications, the team has developed a method that allows them to modify quinolines, small organic molecules with an aromatic nitrogen heterocycle, with B-, Si-, and carbon-containing groups simultaneously.