Ricerc@Sapienza

This paper evaluates the effects of ultrasonication (US) applied, individually or in combination with a mechanical treatment, to the effluent of anaerobic digestion (AD) of lignocellulosic waste, on methane (CH4) production. US of the substrate downstream of AD is a relatively novel concept aimed at improving the degradation of recalcitrant components in order to enhance the overall energy efficiency of the process. US tests were carried out on real digestate samples at different energies (500−50,000 kJ/kg total solids (TS), corresponding to sonication densities of 0.08−0.45 W/ml).

Degradation of post-consumer PLA to lactic acid was analysed in order to assess the economic feasibility of the PLA chemical recycling process. Hydrolysis of PLA, in batch reactor, was analysed in the temperature range of 443-473K, under autogenous pressure and a constant PLA to water ratio (equal to approximately 0.11 by weight), without the use of a catalyst. The experimental results suggest that the complete degradation of PLA can be obtained using relatively low reaction-times with the production of a mixture containing the monomer and traces of the dimer of lactic acid.

The genusTalaromyceshas gained attention due to its ability to produce pigments with potential industrialapplications in different areas. Prosperous application of fungal pigments has challenges to overcome, like de-veloping a cost-effective bioprocess. Using agroindustrial wastes could provide inexpensive substrates and itcontributes to maximize sustainability. Therefore, this study evaluated the feasibility of using corncob as a low-cost substrate for pigment production byTalaromyces atroroseusGH2. An acid hydrolysis treatment was used torelease sugars from corncob.

The antitumor agent 6-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)thio)hexan-1-ol (1) is a potent inhibitor of GSTP1-1, a glutathione S-transferase capable of inhibiting apoptosis by binding to JNK1 and TRAF2. We recently demonstrated that, unlike its parent compound, the benzoyl ester of 1 (compound 3) exhibits negligible reactivity towards GSH, and has a different mode of interaction with GSTP1-1. Unfortunately, 3 is susceptible to rapid metabolic hydrolysis.