No abstract

Previous studies demonstrate anaerobic digestion of hydrothermal liquefaction wastewater (HTL-WW) is significant to the sustainability of algal biofuel development for nutrient reuse and residual energy recovery. HTL-WW contains substantial amounts of residual energy but is toxic to anaerobes. With 6% HTL-WW converted from cyanobacteria (e.g. Spirulina), anaerobes were 50% inhibited. In this study, zeolite, granular activated carbon (GAC), and polyurethane matrices (PM) were used during a two-round anaerobic batch test with HTL-WW, and in the presence of each material, the total methane yields were 136 mL/g COD, 169 mL/g COD, and 168 mL/g COD, respectively, being 11%, 37% and 36% higher than the control. GAC was considered promising due to its highest methane yield of 124 mL/g COD at the second feeding, indicating a good recovery of adsorption capacity. The observed low methane production rates indicated the necessity for anaerobic process optimization. The physicochemical analysis of the digestates demonstrated that most of the compounds identified in the HTL-WW were degraded.

h i g h l i g h t sHydrothermal liquefaction of low-lipid microalgae C. pyrenoidosa. t r a c tThis study investigated the characteristics of aqueous phase from hydrothermal liquefaction of low-lipid microalgae Chlorella pyrenoidosa. The interactions of operating conditions, including reaction temperature, retention time and total solid ratio were evaluated by response surface methodology. The chemical oxygen demand, total nitrogen and total phosphorus were selected as indicators of the property of AP. Results indicated that total solid ratio was found to be the dominant factor affecting the nutrient recovery efficiencies of AP. Based on energy recovery, GC-MS indicated that the AP at two optimized operating conditions (280°C, 60 min, 35 wt.% and 300°C, 60 min, 25 wt.%) were observed to have a higher concentration of organic acids (10.35% and 8.34%) while the sample (260°C, 30 min, 35 wt.%) was observed to have the highest concentration of N&O-heterocyclic compounds (36.16%).