Chemical engineers discover 'ultraselective' process to make valuable chemical from biomass

May 29, 2013

(Phys.org) —Chemical engineering researchers Wei Fan, Paul Dauenhauer and colleagues at the University of Massachusetts Amherst report this week that they've discovered a new chemical process to make p-xylene, an important ingredient of common plastics, at 90 percent yield from lignocellulosic biomass, the highest yield achieved to date. Details are in the current issue of Green Chemistry.

As Dauenhauer explains, the chemical industry currently produces p-xylene from more expensive petroleum, while the new process will make the same chemical from lower-cost, renewable biomass. He and colleagues call the process "ultraselective" because of its ability to achieve 90 percent selectivity for the desired product. "The biomass-derived p-xylene can be mixed with petroleum-based plastics, and consumers will not be able to tell the difference. But manufacturers and chemical companies will be able to operate more sustainably and at lower cost in the future because of this discovery," he adds.

Consumers already know the plastics made from this new process by the triangular recycling label "#1" on . Xylene chemicals are used to produce a plastic called PET (), which is currently used in many products including soda bottles, food packaging, for clothing and even automotive parts, Dauenhauer says.

The UMass Amherst team's discovery reveals the impact of nano-structured catalyst design on renewable chemical processes. Led by Fan, they examined a large number of nano-porous , including zeolites, investigating their capability for producing p-xylene. A specific material identified as 'zeolite beta' was found to be optimal. "We discovered that the performance of the biomass reaction was strongly affected by the nanostructure of the catalyst, which we were able to engineer and achieve 90 percent yield," Fan says.

Explore further: A new approach to creating organic zeolites

More information: pubs.rsc.org/en/content/articl… g/2013/gc/c3gc40740c

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