Muck and Mystery
   Loitering With Intent
blog - at - crumbtrail.org
June 14, 2007
Chemistry . . .

is starting to get interesting.

Glucose, in plant starch and cellulose, is nature’s most abundant sugar. “But getting a commercially viable yield of HMF [hydroxymethylfurfural, a promising surrogate for petroleum-based chemicals] from glucose has been very challenging,” Zhang said. “In addition to low yield until now, we always generate many different byproducts,” including levulinic acid, making product purification expensive and uncompetitive with petroleum-based chemicals. . .

The solvent, called an ionic liquid, enabled the metal chlorides to convert the sugars to HMF. Ionic liquids provide an additional benefit: It is reusable, thus produces none of the wastewater in other methods that convert fructose to HMF.

Metal chlorides belong to a class of ionic-liquid-soluble materials called halides, which “in general work well for converting fructose to HMF,” Zhang said — but not so well when glucose is the initial stock. In fact, attempts at direct glucose conversion created so many impurities that it was simpler to start with the fructose, less common in nature than glucose.

Zhang and his team, working with a high-throughput reactor capable of testing 96 metal halide catalysts at various temperatures, discovered that a particular metal — chromium chloride — was by far the most effective at converting glucose to HMF with few impurities and, as such reactions go, at low temperature, 100 degrees centigrade. . .

The chemistry at work remains largely a mystery, Zhang said, but he suspects that metal chloride catalysts work during an atom-swapping phase that sugar molecules go through called mutarotation, in which an H (hydrogen) and OH (hydroxyl group) trade places.

This sounds a lot better than an ethanol refinery.
Posted by back40 at 07:28 PM | Energy

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