Biomass-based carbon nanofibers (CNF) were synthesized using lignin extracted from sawdust and polyacrylonitrile (PAN) (30:70) with the help of the electrospinning method and subsequent stabilization at 220 °C and carbonization at 800, 900, and 1000 °C. The synthesized CNFs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method. The temperature effect shows that CNF carbonized at 800 °C has excellent stability at different current densities and high capacitance. CNF 800 in the first test cycle at a current density of 100 mA/g shows an initial capacity of 798 mAh/g and an initial coulomb efficiency of 69.5%. The CNF 900 and 1000 show an initial capacity of 668 mAh/g and 594 mAh/g, and an initial Coulomb efficiency of 52% and 51%. With a long cycle (for 500 cycles), all three samples at a current density of 500 mA/g show stable cycling in different capacities (CNF 800 in the region of 300–400 mAh/g, CNF 900 and 1000 in the region of 100–200 mAh/g).

Activated carbons (ACs) have been the most widespread carbon materials used in supercapacitors (SCs) due to their easy processing methods, good electrical conductivity, and abundant porosity. For the manufacture of electrodes, the obtained activated carbon based on sawdust (karagash and pine) was mixed with conductive carbon and polyvinylidene fluoride as a binder, in ratios of 75% activated carbon, 10% conductive carbon black, and 15% polyvinylidene fluoride (PVDF) in an N-methyl pyrrolidinone solution, to form a slurry and applied to a titanium foil. The total mass of each electrode was limited to vary from 2.0 to 4.0 mg. After that, the electrodes fitted with the separator and electrolyte solution were symmetrically assembled into sandwich-type cell construction. The carbon’s electrochemical properties were evaluated using cyclic voltammetry (CV) and galvanostatic charge–discharge (CGD) studies in a two-electrode cell in 6M KOH. The CV and CGD measurements were realized at different scan rates (5–160 mV s⁻¹) and current densities (0.1–2.0 A g⁻¹) in the potential window of 1 V. ACs from KOH activation showed a high specific capacitance of 202 F g⁻¹ for karagash sawdust and 161 F g⁻¹ for pine sawdust at low mass loading of 1.15 mg cm⁻² and scan rate of 5 mV s⁻¹ in cyclic voltammetry test and 193 and 159 F g⁻¹ at a gravimetric current density of 0.1 A g⁻¹ in the galvanostatic charge–discharge test. The specific discharge capacitance is 177 and 131 F g⁻¹ at a current density of 2 A g⁻¹. Even at a relatively high scan rate of 160 mV s⁻¹, a decent specific capacitance of 147 F g⁻¹ and 114 F g⁻¹ was obtained, leading to high energy densities of 26.0 and 22.1 W h kg⁻¹ based on averaged electrode mass. Surface properties and the porous structure of the ACs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method.

Carbon nanofibers based on lignin from wood waste have a promising potential for the ability to produce electrodes that can modernize existing energy storage technology. The most important detail is that the low cost, as well as the availability of the initial products for the production of lignin, will reduce the cost of energy storage devices and contribute to improving the environment. In this study, pine sawdust and elm sawdust were used as raw materials for the production of lignin, which accumulate in large quantities in metal workshops in Almaty. Lignin extraction was carried out using an organosolvent method, which is environmentally friendly, low-cost, uses minimal amounts of strong acids and metal catalysts, does not pollute water, and does not emit sulfur dioxide (SO₂). A comprehensive study of the characteristics of the obtained lignins from wood waste was carried out. Infrared spectroscopy (IR) revealed that the obtained lignin contains aromatic, phenolic, hydroxyl, methyl, and methoxyl groups. The results of nuclear magnetic resonance (NMR) spectroscopy showed the presence of a high number of syringyl (S) links compared to guaiacyl (G), which contribute to increased efficiency in the thermal processing of lignin. Also, this study investigated the use of the obtained lignins to produce continuous fibers by electrospinning. The effect of lignin mass on the viscosity of the lignin/polyacrylonitrile (PAN) solution and the effect of the carbonization temperature on the physico-chemical characteristics of the lignin/PAN solution were investigated. The following research methods were used for this purpose: Raman spectroscopy, thermogravimetric analysis (TGA), electron scanning microscopy, energy dispersion analysis, IR, NMR, and optical microscopy. The conditions for the production of lignin-containing carbon fibers at temperatures of 800, 900, and the carbonation heating rate, is an important parameter in the production of carbon fibers as it strongly affects the characteristics of the resulting carbon fibers. The heating rate affects were studied, and it was found that, at a heating rate of 5 °C/min and a carbonation temperature of 800 °C, porous carbon nanofibers with a diameter of 47 nm are formed in a nitrogen medium for 60 min.

Cu is central to electrification and low-carbon technologies, while declining ore grades and environmental pressures increase interest in recovery from secondary liquid resources. This review critically evaluates copper separation from mine-affected waters, copper-smelting waste acids, electroplating wastewaters, and secondary-material leachates. Cu is the principal target; co-occurring metals are treated as competitors or sequential recovery targets. Feed origin, Cu concentration and speciation, pH/free acidity, ionic strength, ligands, and polymetallic composition are related to process performance and product form. Conventional precipitation, solvent extraction, ion exchange, and electrowinning are compared with microfiltration, ultrafiltration, nanofiltration, reverse osmosis, electrodialysis, supported liquid membranes, emulsion liquid membranes, and polymer inclusion membranes. High Cu removal or rejection does not by itself demonstrate Cu-selective recovery. MF and UF require conversion of dissolved Cu into retainable species; NF and RO mainly recover water and preconcentrate metals; ED becomes more selective with speciation control; and carrier-mediated membranes can fractionate metals but face stability constraints. Most membrane processes generate a Cu-rich retentate, concentrate, or stripping solution rather than metallic Cu and therefore require downstream crystallisation or electrowinning. Key gaps are long-term operation with variable industrial feeds, fouling and scaling control, mass balances and product-purity reporting, membrane/carrier durability, and consistent techno-economic validation.