MIT researchers have produced practical guidelines for generating hydrogen using scrap aluminum and water. First, they obtained specially fabricated samples of pure aluminum and aluminum alloys designed to replicate the types of scrap aluminum typically available from recycling sources. They then demonstrated ways of treating the samples to ensure that the surfaces of all the aluminum “grains” that make up the solid remain free of deposits throughout the reaction. Next, they showed that they could “tune” the hydrogen output by starting with pure aluminum or specific alloys and by manipulating the size of the internal aluminum grains. Such tuning can be used to meet demands for brief bursts of hydrogen, for example, or for lower, longer-lasting flows. The work confirms that, when combined with water, aluminum can provide a high-energy-density, easily transportable, flexible source of hydrogen to serve as a carbon-free replacement for fossil fuels.
As the world works to move away from fossil fuels, many researchers are investigating whether clean hydrogen fuel can play an expanded role in sectors from transportation and industry to buildings and power generation. It could be used in fuel cell vehicles, heat-producing boilers, electricity-generating gas turbines, systems for storing renewable energy, and more.
But while using hydrogen doesn’t generate carbon emissions, making it typically does. Today, almost all hydrogen is produced using fossil fuel–based processes that together generate more than 2% of all global greenhouse gas emissions. In addition, hydrogen is often produced in one location and consumed in another, which means its use also presents logistical challenges.
Another option for producing hydrogen comes from a perhaps surprising source: reacting aluminum with water. Aluminum metal will readily react with water at room temperature to form aluminum hydroxide and hydrogen. That reaction doesn’t typically take place because a layer of aluminum oxide naturally coats the raw metal, preventing it from coming directly into contact with water.
Using the aluminum-water reaction to generate hydrogen doesn’t produce any greenhouse gas emissions, and it promises to solve the transportation problem for any location with available water. Simply move the aluminum and then react it with water on-site. “Fundamentally, the aluminum becomes a mechanism for storing hydrogen—and a very effective one,” says Douglas P. Hart, professor of mechanical engineering. “Using aluminum as our source, we can ‘store’ hydrogen at a density that’s 10 times greater than if we just store it as a compressed gas.”
Two problems have kept aluminum from being employed as a safe, economical source for hydrogen generation. The first problem is ensuring that the aluminum surface is clean and available to react with water. To that end, a practical system must include a means of first modifying the oxide layer and then keeping it from re-forming as the reaction proceeds.
The second problem is that pure aluminum is energy-intensive to mine and produce, so any practical approach needs to use scrap aluminum from various sources. But scrap aluminum is not an easy starting material. It typically occurs in an alloyed form, meaning that it contains other elements that are added to change the properties or characteristics of the aluminum for different uses. For example, adding magnesium increases strength and corrosion-resistance, adding silicon lowers the melting point, and adding a little of both makes an alloy that’s moderately strong and corrosion-resistant.
Despite considerable research on aluminum as a source of hydrogen, two key questions remain: What’s the best way to prevent the adherence of an oxide layer on the aluminum surface, and how do alloying elements in a piece of scrap aluminum affect the total amount of hydrogen generated and the rate at which it is generated?
“If we’re going to use scrap aluminum for hydrogen generation in a practical application, we need to be able to better predict what hydrogen generation characteristics we’re going to observe from the aluminum-water reaction,” says Laureen Meroueh PhD ’20 of mechanical engineering.
Since the fundamental steps in the reaction aren’t well understood, it’s been hard to predict the rate and volume at which hydrogen forms from scrap aluminum, which can contain varying types and concentrations of alloying elements. So Hart, Meroueh, and Thomas W. Eagar SB ’72, ScD ’75, a professor of materials engineering and engineering management in the Department of Materials Science and Engineering, decided to examine—in a systematic fashion—the impacts of those alloying elements on the aluminum-water reaction and on a promising technique for preventing the formation of the interfering oxide layer.
To prepare, they had experts at Novelis Inc. (Spokane, Washington) fabricate samples of pure aluminum and of specific aluminum alloys made of commercially pure aluminum combined with either 0.6% silicon (by weight), 1.0% magnesium, or both—compositions that are typical of scrap aluminum from a variety of sources. Using those samples, the MIT researchers performed a series of tests to explore different aspects of the aluminum-water reaction.
The first step was to demonstrate an effective means of penetrating the oxide layer that forms on aluminum in the air. Solid aluminum is made up of tiny grains that are packed together with occasional boundaries where they don’t line up perfectly. To maximize hydrogen production, researchers would need to prevent the formation of the oxide layer on all those interior grain surfaces.
Research groups have already tried various ways of keeping the aluminum grains “activated” for reaction with water. Some have crushed scrap samples into particles so tiny that the oxide layer doesn’t adhere. But aluminum powders are dangerous, as they can react with humidity and explode. Another approach calls for grinding up scrap samples and adding liquid metals to prevent oxide deposition. But grinding is a costly and energy-intensive process.
To Hart, Meroueh, and Eagar, the most promising approach—first introduced by Jonathan Slocum ScD ’18 while he was working in Hart’s research group—involved pretreating the solid aluminum by painting liquid metals on top and allowing them to permeate through the grain boundaries, as shown in the diagram below.
To determine the effectiveness of that approach, the researchers needed to confirm that the liquid metals would reach the internal grain surfaces, with and without alloying elements present. And they had to establish how long it would take for the liquid metal to coat all of the grains in pure aluminum and its alloys.
They started by combining two metals—gallium and indium—in specific proportions to create a “eutectic” mixture, that is, a mixture that would remain in liquid form at room temperature. They coated their samples with the eutectic and allowed it to penetrate for time periods ranging from 48 to 96 hours. They then exposed the samples to water and monitored the hydrogen yield (the amount formed) and flow rate for 250 minutes. After 48 hours, they also took high-magnification scanning electron microscope (SEM) images so they could observe the boundaries between adjacent aluminum grains.
Based on the hydrogen yield measurements and the SEM images, the MIT team concluded that the gallium-indium eutectic does naturally permeate and reach the interior grain surfaces. However, the rate and extent of penetration vary with the alloy. The permeation rate was the same in silicon-doped aluminum samples as in pure aluminum samples but slower in magnesium-doped samples.
Perhaps most interesting were the results from samples doped with both silicon and magnesium—an aluminum alloy often found in recycling streams. Silicon and magnesium chemically bond to form magnesium silicide, which occurs as solid deposits on the internal grain surfaces. Meroueh hypothesized that when both silicon and magnesium are present in scrap aluminum, those deposits can act as barriers that impede the flow of the gallium-indium eutectic.
The experiments and images confirmed her hypothesis: The solid deposits did act as barriers, and images of samples pretreated for 48 hours showed that permeation wasn’t complete. Clearly, a lengthy pretreatment period would be critical for maximizing the hydrogen yield from scraps of aluminum containing both silicon and magnesium.
Meroueh cites several benefits to the process they used. “You don’t have to apply any energy for the gallium-indium eutectic to work its magic on aluminum and get rid of that oxide layer,” she says. “Once you’ve activated your aluminum, you can drop it in water, and it’ll generate hydrogen—no energy input required.” Even better, the eutectic doesn’t chemically react with the aluminum. “It just physically moves around in between the grains,” she says. “At the end of the process, I could recover all of the gallium and indium I put in and use it again”—a valuable feature as gallium and (especially) indium are costly and in relatively short supply.
The researchers next investigated how the presence of alloying elements affects hydrogen generation. They tested samples that had been treated with the eutectic for 96 hours; by then, the hydrogen yield and flow rates had leveled off in all the samples. The figures below show the impacts on total hydrogen yield (left) and flow rate (right) over time.
As seen in the left-hand figure, the presence of 0.6% silicon (the red curve) increased the hydrogen yield for a given weight of aluminum by 20% compared to pure aluminum (black)—even though the silicon-containing sample had less aluminum than the pure aluminum sample. In contrast, the presence of 1.0% magnesium (dark blue) produced far less hydrogen, while adding both silicon and magnesium (light blue) pushed the yield up but not to the level of pure aluminum.
The right-hand figure shows that the presence of silicon also greatly accelerated the reaction rate, producing a far higher peak in the flow rate but cutting short the duration of hydrogen output. The presence of magnesium produced a lower flow rate but allowed the hydrogen output to remain fairly steady over time. And once again, aluminum with both alloying elements produced a flow rate between that of magnesium-doped and pure aluminum.
Those results provide practical guidance on how to adjust the hydrogen output to match the operating needs of a hydrogen-consuming device. If the starting material is commercially pure aluminum, adding small amounts of carefully selected alloying elements can tailor the hydrogen yield and flow rate. If the starting material is scrap aluminum, careful choice of the source can be key. For high, brief bursts of hydrogen, pieces of silicon-containing aluminum from an auto junkyard could work well. For lower but longer flows, magnesium-containing scraps from the frame of a demolished building might be better. For results somewhere in between, aluminum containing both silicon and magnesium should work well; such material is abundantly available from scrapped cars and motorcycles, yachts, bicycle frames, and even smartphone cases.
It should also be possible to combine scraps of different aluminum alloys to tune the outcome, notes Meroueh. “If I have a sample of activated aluminum that contains just silicon and another sample that contains just magnesium, I can put them both into a container of water and let them react,” she says. “So I get the fast ramp-up in hydrogen production from the silicon and then the magnesium takes over and has that steady output.”
Another practical way to affect hydrogen production could be to reduce the size of the aluminum grains—a change that should increase the total surface area available for reactions to occur.
To investigate that approach, the researchers requested specially customized samples from their supplier. Using standard industrial procedures, the Novelis experts first fed each sample through two rollers, squeezing it from the top and bottom so that the internal grains were flattened. They then heated each sample until the long, flat grains had reorganized and shrunk to a targeted size.
The figures below present results of decreasing grain size. The left-hand figure shows the change in reaction efficiency, defined as the amount of hydrogen formed per gram of aluminum as a percentage of the theoretical maximum. The curves display results calculated using a widely accepted equation that relates yield strength to grain size. The right-hand figure shows the change in reaction duration. As the figures demonstrate, reducing the grain size increased the efficiency and decreased the duration of the reaction to varying degrees in the different samples.
Throughout their experiments, the researchers encountered some unexpected results. For example, standard corrosion theory predicts that pure aluminum will generate more hydrogen than silicon-doped aluminum will—the opposite of what they observed in their experiments.
To shed light on the underlying chemical reactions, Hart, Meroueh, and Eagar investigated hydrogen “flux,” that is, the volume of hydrogen generated over time on each square centimeter of aluminum surface, including the interior grains. They examined three grain sizes for each of their four compositions and collected thousands of data points measuring hydrogen flux.
Their results show that reducing grain size has significant effects. It increases the peak hydrogen flux from silicon-doped aluminum as much as 100 times and from the other three compositions by 10 times. With both pure aluminum and silicon-containing aluminum, reducing grain size also decreases the delay before the peak flux and increases the rate of decline afterward. With magnesium-containing aluminum, reducing the grain size brings about an increase in peak hydrogen flux and results in a slightly faster decline in the rate of hydrogen output. With both silicon and magnesium present, the hydrogen flux over time resembles that of magnesium-containing aluminum when the grain size is not manipulated. When the grain size is reduced, the hydrogen output characteristics begin to resemble behavior observed in silicon-containing aluminum. That outcome was unexpected because when silicon and magnesium are both present, they react to form magnesium silicide, resulting in a new type of aluminum alloy with its own properties.
The researchers stress the benefits of developing a better fundamental understanding of the underlying chemical reactions involved. In addition to guiding the design of practical systems, it might help them find a replacement for the expensive indium in their pretreatment mixture. Other work has shown that gallium will naturally permeate through the grain boundaries of aluminum. “At this point, we know that the indium in our eutectic is important, but we don’t really understand what it does, so we don’t know how to replace it,” says Hart.
But already Hart, Meroueh, and Eagar have demonstrated two practical ways of tuning the hydrogen reaction rate: by adding certain elements to the aluminum and by manipulating the size of the interior aluminum grains. In combination, those approaches can deliver significant results. “If you go from magnesium-containing aluminum with the largest grain size to silicon-containing aluminum with the smallest grain size, you get a hydrogen reaction rate that differs by two orders of magnitude,” says Meroueh. “That’s huge if you’re trying to design a real system that would use this reaction.”
This research was supported through the MIT Energy Initiative by ExxonMobil-MIT Energy Fellowships awarded to Laureen Meroueh PhD ’20 from 2018 through 2020. Meroueh is now CEO of Alchemr, Inc., a startup that is developing the next generation of scalable water electrolyzers for low-cost green hydrogen production. Further information about the research can be found in:
L. Meroueh, T.W. Eagar, and D.P. Hart. “Effects of Mg and Si doping on hydrogen generation via reduction of aluminum alloys in water.” ACS Applied Energy Materials, vol. 3, no. 2, pp. 1860–1868, 2020. Online: doi.org/10.1021/acsaem.9b02300.
L. Meroueh, L. Neil, T.W. Eagar, and D.P. Hart. “Leveraging grain size effects on hydrogen generated via doped aluminum-water reactions enabled by a liquid metal.” ACS Applied Energy Materials, December 2020. Online: doi.org/10.1021/acsaem.0c02175.