Biochar amendment rapidly shifts microbial community structure with enhanced thermophilic digestion activity.

Effects of powdered (<0.075 mm) biochar on thermophilic anaerobic digestion were investigated with biochemical methane potential (BMP) assays. The assays had substrate to inoculum ratios (SIR) of 2.2 and 4.4 g-volatile solids (VS)/g-VS and biochar dosing of 6 g/g-total solids (TS)inoculum. Compared to control, biochar amendment enhanced methane production rates by 94%, 75%, and 20% in assays utilizing substrates of acidified sludge at 70 °C, 55 °C and non-acidified mixed sludge, respectively. All controls experienced acute inhibition with lag phases from 12 - 52 days at SIR of 4.4 g-VS/g-VS, while assays with biochar generated methane from day 4. Biochar addition resulted in a rapid shift in microbial community structure associated with an increase in Methanothermobacteraeae (hydrogenotrophic) and Methanosarcinaceae archaea, as well as various volatile fatty acid (VFA)-degrading and hydrogen-producing bacteria. Biochar presents great potential to tackle VFA accumulation, abbreviate lag phase and increase methane rate, particularly at high organic loadings.

Oxidative degradation of Bisphenol A by carbocatalytic activation of persulfate and peroxymonosulfate with reduced graphene oxide.

In the present study, novel metal-free activation of persulfate (PS) and peroxymonosulfate with reduced graphene oxide (rGO) was investigated to degrade Bisphenol A (BPA), one of the most important endocrine disrupting compounds, from different aqueous matrices, namely distilled water (DW) and municipal wastewater treatment plant effluent (TWW). The home-made rGO was characterize and the effect of oxidant (PS and PMS) and catalyst (rGO) concentrations on BPA degradation rates in DW and TWW samples was examined. Complete BPA degradation occurred in DW and TWW with the PS/rGO treatment system after 10 min and 30 min, respectively, whereas 94% (DW) and 83% (TWW) BPA removals were obtained with PMS/rGO for the same treatment period (BPA = 2 mg/L; rGO = 0.02 g/L; PS = 0.25 mM; PMS = 0.5 mM). The radical quenching experiments demonstrated that the SO4- predominated in the activation of PS and PMS with rGO for BPA removal, however, HO contributed to the catalytic oxidation process but to a lower extend. The reusability test results, where the catalyst was deactivated seriously just after second cycle, highlighted the need for further studies to enhance the stability of rGO. This study represented an environmentally benign and efficient oxidative treatment of BPA along with insights into the rGO activated PS or PMS processes.