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Scientists discover ways to break down Polystyrene waste

ANI | Updated: Mar 20, 2021 17:30 IST

Washington [US], March 20 (ANI): Scientists at the U.S. Department of Energy's Ames Laboratory and their partners from Clemson University have discovered a green, low-energy process to break down polystyrene, a type of plastic that is widely used in foam packaging materials, disposable food containers, cutlery, and many other applications.
Polystyrene is part of a much larger global plastic waste problem. Hundreds of millions of metric tons of polymers are produced each year, a large part of which is discarded after use.
Due to the chemical stability and durability of industrial polymers, plastic waste does not easily degrade in landfills and is often burned, which produces carbon dioxide and other hazardous gases. In order to stop the growing flood of polymer waste and reduce carbon dioxide emissions, plastics have to be recycled or converted into new value-added products.
Currently, recycling of the vast majority of plastics is not economically feasible; their sorting and separation are time and labour-intensive, while chemical processing and remanufacturing require significant energy input and toxic solvents. Re-processed polymers often show inferior performance to that of the freshly manufactured "made from scratch" materials.
A team of scientists at Ames Laboratory used processing by ball-milling to deconstruct commercial polystyrene in a single step, at room temperature, in the ambient atmosphere in the absence of harmful solvents.
Ball-milling is a technique that places materials in a milling vial with metal ball bearings which is then agitated until the desired chemical reaction occurs. Called mechanochemistry, this experimental approach has numerous applications in new materials synthesis and attractive features where plastics recycling is concerned.

The deconstruction of polystyrene proceeds through a series of chemical events involving mechanical cutting apart of the macromolecules, which generates free radicals detectable in the milled material even after its prolonged exposure to air.
The metal bearings used for milling and the ambient oxygen act as co-catalysts that enable extraction of the monomeric styrene from the oligomeric radical-bearing species formed. The experiments showed that the temperature rise in the material during milling is not responsible for the observed phenomenon since the temperature inside the milled powder does not exceed 50oC while the thermal decomposition of polystyrene in the air starts at about 325oC.
Clemson's group confirmed the comprehensive deconstruction of the original polymer into smaller fragments, oligomeric materials, suitable for further processing into new value-added products.
"This method represents an important breakthrough that enables dismantling of a polymer simultaneously with its break-down under ambient conditions, that is, ~300oC below the thermal decomposition temperature of the pristine material," said Ames Laboratory Senior Scientist Viktor Balema. "We think this proof of concept is an exciting possibility for developing new recycling technologies for all kinds of plastics, and that will contribute to the establishment of the circular economy."
His partner from Clemson University, Kentwool Distinguished Professor Igor Luzinov, further commented that "this discovery opens new avenues for low-temperature recovery of monomers from multicomponent polymer-based systems such as composites and laminates. Also, our technology will allow extracting the monomer from crosslinked materials containing styrene units in their structures."
Alfred P. Sloan Foundation Research Fellow, Professor Aaron Rossini of Iowa State University, further noted that "electron paramagnetic resonance spectroscopy shows large concentrations of free radical carbon-centred species in polystyrene that was milled in air.
This is a startling result because free radicals are normally very reactive. Also, the presence of the radicals gives direct evidence that the milling directly causes the scission of the polymer chains. We expect that the reactive sites associated with the free radicals can be used to functionalize the processed polymers to obtain new value-added products." (ANI)