D. Hancu et Ej. Beckman, Production of hydrogen peroxide in liquid CO2. I. Design, synthesis, and phase behavior of CO2-miscible anthraquinones, IND ENG RES, 38(7), 1999, pp. 2824-2832
H2O2 production via sequential hydrogenation-oxidation of anthraquinones (A
Qs) represents a potentially efficient process application of liquid or sup
ercritical CO2 (ScCO2). First, the use of CO2 as the organic solvent in the
process will. eliminate the mass-transfer limitation during the hydrogenat
ion and oxidation and also the contamination of the aqueous phase during is
olation of hydrogen peroxide. Further, the hydrogen peroxide can be recover
ed from CO2 solution without depressurization by liquid-liquid extraction,
helping to minimize the energy cost. The primary obstacle to use CO2 as a w
orking fluid in the process is the poor solubility of conventional AQs in C
O2. Therefore, we designed and generated CO2-philic AQs suitable to be used
in the production of hydrogen peroxide. Both mono- and difunctionalized an
thraquinones (FAQs) were synthesized by attaching CO2-philic polymers chain
s (-CF(CF3)CF2O-) either to mono- or diaminoanthraquinones or to (hydroxyme
thyl)anthraquinone. All. FAQs synthesized are highly soluble in CO2 and pre
sent liquid-liquid phase behavior with minimum miscibility pressure between
170 and 210 bar. Cloud-point pressures were shifted to lower values by usi
ng nonhydrogen bonding linkers between AQ block and CO2-philic tails or by
increasing the CO2-philic content of FAQs.