In the last few years, extensive research efforts have been made to develop novel bio-char-based electrodes using different strategies starting from a variety of biomass precursors as well as applying different thermochemical conversion paths. In this regard, hydrothermal carbonization method is becoming a more prevalent option among conversion procedures even if pyrolysis remains crucial in converting biomass into carbonaceous materials. The main aim of this study is to develop an innovative supercapacitor electrode from spruce bark waste through a unique low-temperature technique approach, which proved to effectively eliminate the pyrolysis step. Consequently, a hybrid spruce-bark-graphene oxide compound (HySB) was obtained as electrode material for supercapacitors. When compared to a regularly used commercial electrode material, SLC1512P graphite (reference) with 150.3 µF cm⁻² capacitance, the HySB has a substantially higher capacitive performance of 530.5 µF cm⁻². In contrast to the reference, the HySB polarization resistance increases by two orders of magnitude at the stationary potential and by three orders of magnitude at the optimum potential, underlying that the superior performances of HySB extend beyond static conditions. The synthesis strategy provides an appropriate energy-efficient option for converting biomass into carbonaceous materials with meaningful properties suitable for energy storage applications.

In the context of sustainable use of resources, hydrothermal conversion of biomass has received increased consideration. As well, the hydrochar (the solid C-rich phase that occurs after the process) has caused great interest. In this work, spruce bark (Picea abies) wastes were considered as feedstock and the influence of hydrothermal process parameters (temperature, reaction time, and biomass to water ratio) on the conversion degree has been studied. Using the response surface methodology and MiniTab software, the process parameters were set up and showed that temperature was the significant factor influencing the conversion, while residence time and the solid-to-liquid ratio had a low influence. Furthermore, the chemical (proximate and ultimate analysis), structural (Fourier-transform infrared spectroscopy, scanning electron microscopy) and thermal properties (thermogravimetric analysis) of feedstock and hydrochar were analyzed. Hydrochar obtained at 280 °C, 1 h processing time, and 1/5 solid-to-liquid ratio presented a hydrophobic character, numerous functional groups, a lower O and H content, and an improved C matter, as well as a good thermal stability. Alongside the structural features, these characteristics endorsed this waste-based product for applications other than those already known as a heat source.

The conversion of lignocellulosic waste ascends as a promising path to generate new materials with wide industrial and environmental uses. Pyrolytic biochar (PBc), hydrochar (Hc), and activated hydrochar (AcHc) produced from the waste of Picea Abies bark were considered bio-based sorbents for lead uptake from aqueous effluents. PBc was obtained through slow pyrolysis (550 °C), while Hc resulted under hydrothermal conversion (280 °C). In order to enhance the specific surface, Hc was subjected to a physical activation, resulting AcHc. All three carbonaceous materials were prepared through relatively simple processes from a readily locally available resource. The carbonaceous materials were characterized using infrared spectroscopy and scanning electron microscopy. The Pb (II) removal has been tested in batch mode on a synthetic monocomponent wastewater matrix, as well as on a real mine drainage effluent. A significant effect of pH was observed, while the equilibrium was achieved in a short time, about 60 min for PBc and Hc and 120 min for AcHc. Langmuir model predicted a maximum adsorption capacity of 15.94 mg/g for PBc, 9.99 mg/g for Hc, and 37.46 mg/g for AcHc. All materials studied had good uptake capacities for lead with no drastic effect of typical coexisting species.

The relative performance of different porous solids in different applications is highly dependent on the internal pore structure of each material. Highly porous carbon materials can be prepared by evaporative drying and the pyrolysis of resorcinol-formaldehyde gels. By determining the correct synthesis parameters, the pore system of such materials can be reshaped. Depending on some important processing factors such as the dilution ratio or the initial pH of the precursor solution, various porous or non-porous carbon materials can be synthesized. This paper addresses carbon xerogels (CX) designed as a material electrode in capacitive deionization (CDI) systems for water desalination. In this work CX materials were synthesized via poly-condensation reactions of resorcinol with formaldehyde (RF) on a carbon felt sheet followed by pyrolysis. The resulting sheets were used as electrodes to develop a CDI experimental multi-cell laboratory system. The initial pH of the RF solution and the dilution ratio effect on the resulting carbon surface area and structure were analyzed. Surface area measurements using the BET method and an electrochemical capacitance evaluation of the obtained xerogels through electrochemical impedance spectroscopy were also performed. Finally, using our experimental CDI multi-cell laboratory system based on the obtained CX, we discuss the experimental data for the desalination rate as a function of the voltage and salt concentration. As a result, the developed model’s efficiency is demonstrated. The main goal of this work was to develop an efficient electrode-based novel carbon that could be commercially competitive, as well as to create guidelines for future desalination research using CX electrode materials.