Vivianite presents a significant phosphorus pool in iron-rich, reducing environments, necessitating the development of an affordable and routine quantification method. A novel extraction protocol using 2,2′-bipyridine (Bipy) was proposed as a promising approach. However, the efficacy of this protocol in achieving complete vivianite extraction remains uncertain and lacks robust analytical validation.

This study systematically assessed the Bipy extraction protocol on known amount of synthetic and two magnetically recovered environmental vivianite samples, with varying oxidation levels, impurity content, and particle size. Extraction efficiencies of iron and phosphorus were 13–44 % and 13–55 %, respectively, indicating incomplete extraction under the original protocol conditions (0.2 % Bipy, 24 h). An initially rapid release of iron and phosphorus slowed down across all samples, indicating non-constant reaction rates, and suggesting that the extraction is governed by mechanisms beyond kinetic control. Extending the extraction time to 48 h and increasing the Bipy concentration to 1 % yielded marginal improvements, with efficiency gains of 14 % or less. Grinding, which reduced particle size, nearly doubled extraction efficiency. Conversely, the sample with the highest Fe2+ content showed the overall lowest overall extraction efficiencies. Similarly, recovered vivianite samples containing impurities, namely magnesium and calcium, were extracted less efficiently than synthetic vivianite. Additionally, the extracted iron-to‑phosphorus ratio exceeded the theoretical value of 0.67, indicating non-stoichiometric extraction.

To establish Bipy extraction as a reliable analytical method, it is crucial to address incomplete extraction and determine whether vivianite can be fully extracted or only to a certain extent. A potential strategy involves reducing extraction time and repeating the extraction step.

Inhibition effect of humic acid (HA) on anaerobic digestion of cellulose and xylan and the mitigation potential of the inhibition were evaluated in controlled fed batch reactors at 30 °C and a hydraulic retention time (HRT) of 20 days. Reactor performances were evaluated by biogas production and metabolite measurements for 220 days. Microbial population dynamics of the reactors were monitored with next-generation 16S rRNA gene sequencing at nine different sampling times. Our results showed that increasing levels of HA inhibited the hydrolysis efficiency of the digestion by 40% and concomitantly reduced the methane yield. Addition of hydrolytic enzymes helped to reverse the negative effects of HA, whereas calcium addition did not reverse HA inhibition. Microbiological analyses showed that the relative abundance of hydrolytic/fermentative bacterial groups such as Clostridiales, Bacteroidales and Anaerolineales was significantly lowered by the presence of HA. HA also affected the archaeal populations. Mostly hydrogenotrophic methanogens were negatively affected by HA. The relative abundance of Methanobacteriaceae, Methanomicrobiales-WCHA208 and Unassigned Thermoplasmata WCHA1-57 were negatively affected by the presence of HA, whereas Methanosaetacea was not affected.