The activity of the heterometallic alkoxide [FeCl{Ti2(OiPr)9}] (1) towards polymerization of rac-lactide (rac-LA) and ε-caprolactone (ε-CL) was investigated in toluene solution and in bulk at various temperatures, monomer/heterometallic alkoxide molar ratio and reaction times. The alkoxide 1 was active in solution for ε-CL and in bulk for both monomers. Polymers were obtained in good yields with molecular weights ranging from 3890 to 15000 g moL-1 and polydispersity indexes (PDI) values varying from 1.3 to 2.5. Based on the 1H nuclear magnetic resonance (NMR) end-group analysis of polymers, a coordination-insertion mechanism was suggested for both monomers. The average number of growing chains per molecule of initiator (4 to 5 for rac-LA and 7 to 8 for ε-CL) indicates that both bridging and terminal isopropoxides are active initiating groups. Kinetic studies with ε-CL indicated that the polymerization rate is first order with respect to monomer concentration. The catalytic properties of 1 were compared to those found for other titanium(IV) and iron(II) complexes using ε-CL as a model monomer.

The effect of moisture content in the steam treatment and enzymatic hydrolysis of sugarcane bagasse was evaluated. Steam treatment was perfomed at 195-210 ºC for 4-8 min using cane bagasse with moisture contents in the range 16-100 wt% (dry basis). Increased moisture contents not only had a positive influence in recovery of main cane biomass components but also resulted in better substrates for enzymatic hydrolysis. As a result, drying is not required for optimal pretreatment and enzymatic hydrolysis of sugarcane bagasse, which can be processed into second generation ethanol immediately after crushing and hot water washing.