Lignin as a polymer of monomeric aromatic compounds retains great potential to be a source for liquid fuels and valuable chemicals. However, lignin from biomass has been traditionally treated as a waste byproduct and in most applications burned for its heat value. In this work, we report the catalytic conversion of lignin in Miscanthus into aromatic products by using earth-abundant Ni catalyst supported on activated carbon, under relatively mild conditions. The special ferulate linkage in grasses gives methyl ferulate ester and its derivatives, which were not observed for wood biomass substrates. By modification of the reaction conditions, saturated or unsaturated branched products can be obtained selectively. Optimal conditions give over 68% yield of select aromatic products from lignin. Furthermore, after lignin depolymerization and upgrading, the carbohydrates of miscanthus were recovered as a solid residue, which upon treatment with iron chloride produced useful platform chemicals (furfurals and levulinic acid). On the basis of our study, all three major components of biomass (lignin, cellulose and hemicellulose) are effectively utilized, with an overall 55% conversion of total accessible biomass into high value chemicals with 98% mass balance.

The high performance multi-walled carbon nanotubes (MWNTs) reinforced epoxy polymer nanocomposites (PNCs) have been synthesized at different MWNT loading levels. The surface functionalization of MWNTs with conductive PANI was achieved by using a facile surface initiated polymerization method with the aid of the oxidations of CNTs and subsequent anilines by hexavalent chromium (Cr(VI)) oxidant. The effects of MWNT loading, surface functionalization and temperature on the rheological behaviors of liquid epoxy resin nanosuspensions and on the physicochemical properties of cured solid PNCs were systematically investigated. The glass transition temperature (T g ) of the cured epoxy PNCs filled with functionalized MWNTs obtained from the dynamic mechanical analysis (DMA)test was increased about 6-25 C than that of cured pure epoxy. The PNCs reinforced with functionalized MWNTs demonstrated an enhanced tensile strength than either cured pure epoxy or its PNCs filled with the as-received MWNTs. The electrical conductivity of cured epoxy PNCs with functionalized MWNTs was improved by 5.5 orders of magnitude compared with cured pure epoxy.Thermogravimetric analysis (TGA) revealed an enhanced thermo-stability in the cured epoxy PNCs filled with functionalized MWNTs than that of cured pure epoxy and its PNCs filled with the as-received MWNTs. The observed strong interfacial interaction between MWNTs and the epoxy resin matrix was responsible for the enhanced mechanical tensile strength. The nanocomposite formation mechanism is proposed based on the analysis from Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman and differential scanning calorimetry (DSC) tests.

Maleic acid (MA) and AlCl 3 self-assemble into catalytic complexes (Al-(MA) 2 -(OH) 2 (aq)) with improved selectivity for converting glucose to HMF, and levulinic acid. The calculated activation energy (E a ) of the MA-aluminum catalyzed glucose-to-fructose isomerization is 95 kJ·mol -1 compared to 149 kJ·mol -1 for HCl and AlCl 3 alone. Furthermore, conversion of fructose to HMF is enhanced. The catalytic conversion of fructose to HMF by MA and AlCl 3 at 180 o C is 1.7× faster