Microwave assisted and conventional hydrothermal treatment of waste seaweed: Comparison of hydrochar properties and energy efficiency.

Waste seaweed is a valuable source for converting into value-added carbon materials. In this study, the production of hydrochar from waste seaweed was optimized for hydrothermal carbonization in a microwave process. The produced hydrochar was compared with hydrochar synthesized by the regular process using a conventional heating oven. The results show that hydrochar produced with a holding time of 1 h by microwave heating has similar properties to the hydrochar produced in a conventionally heated oven for 4 h (200 °C and water/biomass ratio 5): carbon mass fraction (52.4 ± 3.9 %), methylene blue adsorption capacity (40.2 ± 0.2 mg g-1) and similar observations on surface functional groups and thermal stability were made between hydrochars produced by both methods. The analysis of energy consumption showed microwave assisted carbonization consume higher energy in compare to conventional oven. The present results suggest that hydrochar made from waste seaweed and using the microwave technique could be an energy-saving technology for producing hydrochar with similar specifications to hydrochar produced by conventional heating methods.

Cell Behavior Changes and Enzymatic Biodegradation of Hybrid Electrospun Poly(3-hydroxybutyrate)-Based Scaffolds with an Enhanced Piezoresponse after the Addition of Reduced Graphene Oxide.

This is the first comprehensive study of the impact of biodegradation on the structure, surface potential, mechanical and piezoelectric properties of poly(3-hydroxybutyrate) (PHB) scaffolds supplemented with reduced graphene oxide (rGO) as well as cell behavior under static and dynamic mechanical conditions. There is no effect of the rGO addition up to 1.0 wt% on the rate of enzymatic biodegradation of PHB scaffolds for 30 d. The biodegradation of scaffolds leads to the depolymerization of the amorphous phase, resulting in an increase in the degree of crystallinity. Because of more regular dipole order in the crystalline phase, surface potential of all fibers increases after the biodegradation, with a maximum (361 ± 5 mV) after the addition of 1 wt% rGO into PHB as compared to pristine PHB fibers. By contrast, PHB-0.7rGO fibers manifest the strongest effective vertical (0.59 ± 0.03 pm V-1 ) and lateral (1.06 ± 0.02 pm V-1 ) piezoresponse owing to a greater presence of electroactive ß-phase. In vitro assays involving primary human fibroblasts reveal equal biocompatibility and faster cell proliferation on PHB-0.7rGO scaffolds compared to pure PHB and nonpiezoelectric polycaprolactone scaffolds. Thus, the developed biodegradable PHB-rGO scaffolds with enhanced piezoresponse are promising for tissue-engineering applications.

Improving biochar properties by co-pyrolysis of pig manure with bio-invasive weed for use as the soil amendment.

Over recent years, pyrolysis has grown into a mature technology with added value for producing soil improvers. Further innovations of this technology lie in developing tailor-made products from specific feedstocks (or mixtures thereof) in combination with adjusted mixing ratio-temperature regimes. In this context, co-pyrolysis of pig manure (PM) and the invasive plant Japanese knotweed (JK) at different mixture ratios (w/w) of 3:1 (P3J1), 1:1 (P1J1), and 1:3 (P1J3) and varying temperatures (400-700 °C) was studied to address the low carbon properties and heavy metals (HMs) risks of manure-derive biochars and beneficially ameliorate the bio-invasion situation by creating value from the plant biomass. Co-pyrolysis of PM with JK increased by nearly 1.5 folds the fixed carbon contents in the combined feedstock biochars obtained at 600 °C compared with PM-derived biochar alone, and all combined feedstock biochars met the requirements for soil improvement and carbon sequestration. The total HMs in PM biochars were significantly reduced by adding JK. The combined feedstock biochar P1J1 generated at 600 °C was the most effective in transforming Cu and Zn into more stable forms, accordingly reducing the associated environmental risk of heavy metal leaching from the biochar. In addition, the accumulation of macronutrients can be an added benefit of the co-pyrolysis process, and P1J1-600 was also the biochar that retained the most nutrients (P, Ca, Mg, and K).

Biochar and activated carbon enhance ethanol conversion and selectivity to caproic acid by Clostridium kluyveri.

Syngas from biomass or steel mills can be fermented into a dilute stream of ethanol and acetic acid, which requires energy intensive distillation for product recovery. This can be circumvented by selective secondary fermentation of the syngas fermentation effluent to caproic acid as easier recoverable platform chemical with Clostridium kluyveri. Here, we explore the impact of biochar and activated carbon on this process. Changes during the fermentation with biochar or activated carbon were monitored, different doses were tested and the recyclability of biochar and activated carbon was assessed. Biochar decreased the lag phase and increased the caproic acid production rate (up to 0.50 g·L-1·h-1). Upon recycling for subsequent fermentation, biochar retained this property largely. Activated carbon addition, especially at high dose, could potentially increase the conversion and selectivity towards caproic acid to 14.15 g·L-1 (control: 11.01 g·L-1) and 92% (control: 84%), respectively.

Effluent recirculation enables near-complete oxidation of organics during supercritical water oxidation at mild conditions: A proof of principle.

This work presents a continuous set-up for SCWO, which was operated at mild conditions (380 °C, 25 MPa, oxidant equivalence ratio of 2.0 and residence time of 26 s) to oxidize cellulose, lignin, and acetic acid as model compounds. The aim was to oxidize different organics consecutively to near completion in the same mild reaction conditions and set-up. These conditions can overcome some drawbacks associated to SCWO. To combine near complete oxidation with the applied mild process conditions, aqueous effluent from SCWO, containing intermediates from incomplete oxidation, was recycled for consecutive oxidation. Meanwhile, fresh feedstock was continuously fed to retain the process capacity. Upon recycling the aqueous effluent three to four times, depending on the feedstock, the oxidation efficiency increased from 63.9%, 45.3% and 28.3% in a single pass for cellulose, lignin, and acetic acid, respectively, to near 100%. The principle of effluent recirculation should allow a compact set-up to perform almost complete oxidation of different organics at mild conditions. The principles and effects of effluent recirculation are outlined, as well as practical consequences and perspectives of this novel principle to SCWO.

Targeted poly(3-hydroxybutyrate-co-3-hydroxyvalerate) bioplastic production from carbon dioxide.

A microbial production process was developed to convert CO2 and valeric acid into tailored poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) bioplastics. The aim was to understand microbial PHBV production in mixotrophic conditions and to control the monomer distribution in the polymer. Continuous sparging of CO2 with pulse and pH-stat feeding of valeric acid were evaluated to produce PHBV copolyesters with predefined properties. The desired random monomer distribution was obtained by limiting the valeric acid concentration (below 1 gL-1). 1H-NMR, 13C-NMR and chromatographic analysis of the PHBV copolymer confirmed both the monomer distribution and the 3-hydroxyvalerate (3HV) fraction in the produced PHBV. A physical-based model was developed for mixotrophic PHBV production, which was calibrated and validated with independent experimental datasets. To produce PHBV with a predefined 3HV fraction, an operating diagram was constructed. This tool was able to predict the 3HV fraction with a very good accuracy (2% deviation).