Adapted from this Berkeley Lab press release
A new chemical process can essentially vaporize plastics that dominate the waste stream today and turn them into hydrocarbon building blocks for new plastics.
The catalytic process, developed by a team of Foundry users, works equally well with the two dominant types of post-consumer plastic waste: polyethylene, the component of most single-use plastic bags; and polypropylene, the stuff of hard plastics, from microwavable dishes to luggage. It also efficiently degrades a mix of these types of plastics. Their results were recently published in the journal Science.
The process, if scaled up, could help bring about a circular economy for many throwaway plastics, with the plastic waste converted back into the monomers used to make polymers, thereby reducing the fossil fuels used to make new plastics. Clear plastic water bottles made of polyethylene terephthalate (PET), a polyester, were designed in the 1980s to be recycled this way. But the volume of polyester plastics is minuscule compared to that of polyethylene and polypropylene plastics, referred to as polyolefins.
“We have an enormous amount of polyethylene and polypropylene in everyday objects, from lunch bags to laundry soap bottles to milk jugs — so much of what’s around us is made of these polyolefins,” said John Hartwig, a Foundry user as well as a senior faculty scientist in Berkeley Lab’s Chemical Sciences Division and a UC Berkeley professor of chemistry who led the research. “What we can now do, in principle, is take those objects and bring them back to the starting monomer by chemical reactions we’ve devised that cleave the typically stable carbon-carbon bonds. By doing so, we’ve come closer than anyone to give the same kind of circularity to polyethylene and polypropylene that you have for polyesters in water bottles.”
Polyethylene and polypropylene plastics constitute about two-thirds of post-consumer plastic waste worldwide. About 80% ends up in landfills, is incinerated or simply tossed into the streets, often ending up as microplastics in streams and the ocean. The rest is recycled as low-value plastic, becoming decking materials, flowerpots and sporks.
To reduce this waste, researchers have been looking for ways to turn the plastics into something more valuable, such as the monomers that are polymerized to produce new plastics. This would create a circular polymer economy for plastics, reducing the need to make new plastics from petroleum, which generates greenhouse gases.
Two years ago, Hartwig and his team came up with a process for breaking down polyethylene plastic bags into the monomer propylene — also called propene — that could then be reused to make polypropylene plastics. This chemical process employed three different bespoke heavy metal catalysts: one to add a carbon-carbon double bond to the polyethylene polymer and the other two to break the chain at this double bond and repeatedly snip off a carbon atom and, with ethylene, make propylene (C3H6) molecules until the polymer disappeared. But the catalysts were dissolved in the liquid reaction and short-lived, making it hard to recover them in an active form.
In the new process, the expensive, soluble metal catalysts have been replaced by cheaper solid ones commonly used in the chemical industry for continuous flow processes that reuse the catalyst. Continuous flow processes can be scaled up to handle large volumes of material.
Synthesizing a catalyst of sodium on alumina, they found that it efficiently broke or cracked various kinds of polyolefin polymer chains, leaving one of the two pieces with a reactive carbon-carbon double bond at the end. A second catalyst, tungsten oxide on silica, added the carbon atom at the end of the chain to ethylene gas, which is constantly streamed through the reaction chamber to form a propylene molecule. The latter process, called olefin metathesis, leaves behind a double bond that the catalyst can access again and again until the entire chain has been converted to propylene.
The same reaction occurs with polypropylene to form a combination of propene and a hydrocarbon called isobutylene. Isobutylene is used in the chemical industry to make polymers for products ranging from footballs to cosmetics and to make high-octane gasoline additives.
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Surprisingly, the tungsten catalyst was even more effective than the sodium catalyst in breaking polypropylene chains.
“You can’t get much cheaper than sodium,” Hartwig said. “And tungsten is an earth-abundant metal used in the chemical industry in large scale, as opposed to our ruthenium metal catalysts that were more sensitive and more expensive. This combination of tungsten oxide on silica and sodium on alumina is like taking two different types of dirt and having them together disassemble the whole polymer chain into even higher yields of propene from ethylene and a combination of propene and isobutylene from polypropylene than we did with those more complex, expensive catalysts.”
One key advantage of the new catalysts is that they avoid the need to remove hydrogen to form a breakable carbon-carbon double bond in the polymer, which was a feature of the researchers’ earlier process to deconstruct polyethylene. Such double bonds are an Achilles heel of a polymer, in the same way that the reactive carbon-oxygen bonds in polyester or PET make the plastic easier to recycle. Polyethylene and polypropylene don’t have this Achilles heel — their long chains of single carbon bonds are very strong.
The two catalysts together turned a nearly equal mixture of polyethylene and polypropylene into propylene and isobutylene — both gases at room temperature — with an efficiency of nearly 90%. For polyethylene or polypropylene alone, the yield was even higher.
Read the full press release.
