Solketal, also known as 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane, is the main product of the ketalization reaction between glycerol and acetone. This compound can be used as a fuel additive; however, it cannot be blended with diesel in proportions higher than 5% due to physicochemical limitations.
An alternative approach is its alkylation to produce solketal tert-butyl ether (STBE), a compound that is not commercially available and for which, limited information is found in the literature, but which can be used as an oxygenated fuel additive due to its higher physicochemical affinity with diesel.
This work focuses on optimizing STBE synthesis. The conventional route (1) involves ketalization of 1-mono glycerol tert-butyl ether (1-m-GTBE) with acetone followed by isolation of STBE through Column Chromatography, a complex process with high solvent consumption. To reduce the number of steps, two alternative routes were studied: (2) synthesis from a mixture of MTBGs and h-GTBEs, avoiding chromatographic separation after glycerol etherification with tert-butanol; and (3) direct reaction between glycerol, tert-butanol, and acetone with unreacted glycerol removed by liquid-liquid extraction. All three processes were economically evaluated considering reagent, solvent, and energy consumption.
The fractions obtained from the three routes were blended with diesel at 5% v/v and their physicochemical properties were analyzed, confirming compliance with fuel standards (UNE-EN 590:2022). Their performance was evaluated in a diesel engine coupled to an AYERBE generator (5 kVA, 230 V).
Results showed that all three routes reduced pollutant emissions, in some cases substantially, compared to conventional diesel, without significantly affecting engine power output. The economic study indicated that routes 2 (0.88 €/mL) and 3 (0.89 €/mL) substantially lowered costs relative to route 1 (2.54 €/mL). Although product purity decreased, no significant differences were observed in engine performance.