Yerlan Doszhanov

This review critically examines physical and chemical strategies used to enhance the adsorption of CO₂, volatile organic compounds (VOCs), SO₂ and H₂S by biochar-based sorbents. The literature indicates that adsorption performance is governed by the combined effects of feedstock properties, thermochemical conversion conditions, pore structure, surface area and surface chemistry. Physical activation, particularly with steam or CO₂, primarily promotes pore development and increases accessible surface area, whereas chemical treatments with KOH, H₃PO₄, H₂SO₄, amine-based compounds, and biopolymers can additionally modify surface functionality and gas–surface interactions. Across the reviewed studies, KOH activation and nitrogen functionalization are frequently associated with enhanced CO₂ uptake, while acidic surface modification can improve interactions with selected polar VOCs. For sulfur-containing gases, pore development together with appropriate surface functional groups can facilitate both physical adsorption and surface reactions. Rather than identifying a universally optimal modification route, the available evidence shows that sorbent design should be tailored to the physicochemical properties of the target gas. The review also examines biomass residues as precursors and key technical factors affecting the scalability of biochar-based gas purification systems. Overall, the literature highlights biochar’s potential for gas adsorption and the need for evaluation of modification strategies and validation under realistic conditions.

This study explores the possibility of making cardboard and molded egg carton packaging from corn residues and common reed as alternatives to wood-based pulp. Six formulations were made: corn husks (CHs), corn leaves (CLs), corn leaves (35%) plus corn husks (30%) and a corn blend (15%) of wollastonite (CaSiO₃) (CH + CL + W), a corn blend (CH + CL: husks 60%, leaves 40%), mixed corn waste (MCW) and shredded common reed (SR). Optical microscopy was used to evaluate the fiber morphology, including the calculation of the flexibility coefficient, the cell wall rigidity and the Runkel ratio, for raw materials and fiber after alkaline hydrolysis and casting of egg cartons in silicone molds. The grammage, burst strength and index, folding endurance, thickness and moisture content were measured in the cardboard samples, while warping, compressive deformation, moisture and ink absorption were measured in the egg cartons. The flexibility coefficient of the common reed fibers (64.5%) was better than that of the corn fibers (23.6%), and so was the Runkel ratio (0.86 vs. 1.2). In the case of cardboard formulations, the maximum burst strength (462.4 kPa) and the maximum burst index (3.0 kPa·g/m²) values were obtained with the MCW formulation, and the highest folding endurance (42 and 38 double folds) was obtained with the CH and SR formulations, respectively. The addition of wollastonite improved folding endurance to 28 double folds and reduced moisture content to 4.1%, whereas the moisture content was reduced but burst strength decreased to 250.5 kPa. Egg cartons made from corn were found to satisfy all the requirements tested for good packaging, while the reed-based cartons were found to have inadequate ink absorbency time (20 min), making them less printable. Overall, mixed corn residues seem to be the most promising raw materials for sustainable packaging, and wollastonite can be used to adjust the flexibility–strength balance.

Ammonium nitrogen (NH₄⁺-N) is a key biogenic pollutant in aquatic systems. This study evaluated natural diatomite (Aktobe region) and zeolite (Shankhanai, Zhetysu region) as low-cost, environmentally benign sorbents for NH₄⁺-N removal, and examined the effects of thermal (200–750 °C; 450 °C selected) and alkaline (0.5 M NaOH) treatments on their structural, textural and adsorption properties. Materials were characterized by XRD, XRF, FTIR, SEM-EDX and adsorption performance was assessed by kinetic and equilibrium experiments. Specific surface area and pore characteristics were determined from low-temperature nitrogen adsorption–desorption measurements, and the specific surface area was calculated using the Brunauer–Emmett–Teller (BET) method. Thermal treatment at 450 °C increased the specific surface area of diatomite (46.3 m²/g) and pore volume, and subsequent alkaline activation further enhanced adsorption activity. The modified diatomite achieved up to 84.6% removal of NH₄⁺-N with an equilibrium capacity q_max = 1.758 mg/g. Adsorption kinetics were best described by the pseudo-second-order (PSO) model, which may indicate a substantive role of surface chemical interactions. Equilibrium data were fitted with Langmuir and Freundlich models: the modified diatomite fitted Langmuir best (R² = 0.999), which may suggest predominance of a monolayer adsorption mechanism under the studied conditions, whereas natural samples and the zeolite were better described by the Freundlich model, reflecting likely surface energetic heterogeneity. Separation factor values (R_L = 0.068–0.643) indicate favorable adsorption within the investigated concentration range. The point of zero charge (pHpzc) was determined for all sorbents (5.3–6.3), confirming that at pH 7 the surface carries a negative charge favorable for electrostatic attraction of NH₄⁺ cations. Reusability tests over five consecutive adsorption–desorption cycles showed that modified diatomite and modified zeolite retained 93.4% and 92.3% of their initial removal efficiency, respectively, indicating acceptable stability under the applied regeneration conditions. These results demonstrate the potential of alkaline-modified diatomite and zeolite as effective sorbents for ammonium removal from wastewaters, contributing to the mitigation of eutrophication risks.

This study evaluates the effectiveness of natural zeolite (Shankhanai deposit, Kazakhstan) as a functional hydroponic substrate compared to a commercial foamed-glass control (GrowPlant). Using the Nutrient Film Technique (NFT), we assessed the growth and metabolic responses of Medicago sativa L. and three cultivars of Lactuca sativa L. Brunauer–Emmett–Teller (BET) analysis confirmed that zeolite (particle size 3.70 ± 1.20 mm) possesses a high specific surface area (21.80 m²/g), significantly exceeding the control (0.49 m²/g). This structure ensured superior moisture retention and cation exchange, even after a moderate decrease in surface area to 16.66 m²/g post-cultivation due to organic pore-filling. In M. sativa experiments, zeolite increased seedling viability and promoted a more branched root system compared to the artificial substrate. Gas chromatography–mass spectrometry (GC–MS) metabolic profiling of L. sativa revealed a significant substrate-driven reprogramming: zeolite increased the relative proportion of fatty acids and their derivatives (up to +51.27% in May King variety roots), suggesting membrane-protective adaptation. Genotype-specific responses were observed, with the Yeralash cultivar showing increased polyol synthesis (+2.93%) for osmoregulation. The results demonstrate that natural zeolite is an efficient, stable substrate for intensive hydroponics, optimizing root development and physiological stability through enhanced nutrient and water management.

This study presents the development of an environmentally benign and economically viable methodology for the synthesis of graphene-containing carbon materials derived from renewable agricultural residues, specifically walnut shells, rice husks, and apricot stones. The proposed synthesis route involves sequential stages of controlled pre-carbonization, desilicification, chemical activation with potassium hydroxide (KOH), and subsequent mild exfoliation, resulting in the formation of few-layer graphene with a high degree of structural ordering. Pre-carbonization carried out at 523–573 K, followed by activation at 1123 K, yields graphene sheets exhibiting a specific surface area of 1300–1800 m²/g, a carbon content of 60–90%, and an average pore diameter below 100 nm. The synthesized materials were subjected to comprehensive physicochemical characterization using BET surface area analysis, Raman spectroscopy, FTIR spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic absorption flame emission spectrophotometry. Raman spectroscopic analysis revealed an I_G/I_2D intensity ratio of approximately 1.5–2.0, indicating the presence of graphene structures consisting of approximately four to five layers. To enhance adsorption performance, the graphene-containing carbon materials were further functionalized with sulfuric acid, and the successful incorporation of surface functional groups was confirmed by FTIR spectroscopy. The adsorption properties of the functionalized graphene-containing carbon materials were evaluated in aqueous solutions containing sodium, potassium, calcium, and magnesium salts, demonstrating adsorption efficiencies of up to 80%. Compared to conventional biomass-derived graphene synthesis methods, the developed approach produces materials with enhanced porosity, higher graphitic ordering, and improved chemical purity. These characteristics highlight the strong potential of the synthesized graphene-containing carbon materials for applications in energy storage systems, adsorption-based water purification technologies, and environmentally sustainable nanotechnological applications.

This review presents a modern comprehensive analysis of the physicochemical characteristics of carbon materials for the sorption of gases. The main classes of carbon sorbents are considered as follows: nanotubes, activated carbon, graphene, fullerene, composite materials, and organic vapors. Modern methods of modification of carbon materials are systematized. Particular attention is paid to the effect of particle size, morphology, and porous structure on the kinetics and equilibrium characteristics of adsorption. The results of experimental and theoretical studies of the adsorption of the gases (CO₂, SO₂, NO_x, H₂S, NH₃, and CO) are analyzed. A comparative economic analysis of carbon materials is carried out, taking into account the cost of production and estimated costs of modification. Modern areas of application of carbon sorbents are analyzed as follows: industrial gas purification, automotive filters, air conditioning systems, personal protective equipment, and gas sensors. Particular attention is paid to the study of the prospects and future of materials. Prospective development directions are considered, including the creation of hierarchically porous structures, the development of self-healing materials, and integration with artificial intelligence to optimize adsorption processes. The cost of graphene and nanotube production is predicted to decrease by 50–70% by 2030, which will lead to an expansion of their commercial application.

In Kazakhstan, food safety is a pressing issue due to water and soil pollution. This study examined the effect of natural zeolite as an alternative hydroponic substrate on the physicochemical properties of the medium and the physiological and metabolic responses of two agricultural crops: Medicago sativa L. and Lactuca sativa L. BET analysis revealed that the zeolite possesses a substancial specific surface area (22 m²/g), ensuring effective moisture retention and gradual nutrient release. After plant cultivation, these parameters decreased moderately, confirming the filling of the pores with organic compounds without loss of key properties. In experiments with Medicago sativa, zeolite provided better aeration and stable moisture, promoting the development of a branched root system and increased seedling viability compared to an artificial substrate. Metabolic analysis of three Lactuca sativa varieties revealed cultivar-specific adaptive responses. Zeolite increased the synthesis of fatty acids and their derivatives, reflecting membrane-protective restructuring, while sugar and terpenoid content varied depending on the variety. The results confirm the suitability of zeolite as a stable substrate for hydroponic production, allowing for optimized water consumption, improved root development, and enhanced physiological stability of plants.

P-cresol, indole and indole-3-acetic acid (IAA) are catabolites of amino acids, formed by the gut microbiome. Most of these aromatic hydrocarbon derivatives are excreted by the colon before reentering the body to form “exogenous” protein-bound uremic toxins (PBUTs), which aggravate chronic kidney disease (CKD). Removal efficiencies of these PBUT precursors from model phosphate-buffered saline solutions by three different surface-modified nanoporous carbon adsorbents (PCs) were studied. PCs were produced by physicochemical and/or acid base activation of carbonized rice husk waste. Removal rates achieved values of 32–96% within a 3 h contact time. High micro/mesoporosity and surface chemistry of the N- and P-doped biochars were established by N₂ adsorption studies, SEM/EDS analysis, XPS and FT-IR-spectroscopy. The ammoxidized PC-N1 had the highest adsorption capacity (1.97 mmol/g for IAA, 2.43 mmol/g for p-cresol and 2.42 mmol/g for indole), followed by “urea-nitrified” PC-N2, whilst the phosphorylated PC-P demonstrated the lowest adsorption capacity for these solutes. These results do not correlate with the total pore volume values for PC-N2 (0.91 cm³/g) < PC-P (1.56 cm³/g) < PC-N1 (1.84 cm³/g), suggesting that other parameters such as the micropore volume (PC-N1 > PC-N2 > PC-P) and the interaction of surface chemical functional groups with the solutes play key roles in the adsorption mechanism. N-doped PC-N1 and PC-N2 have basic functional groups with higher affinity with acidic IAA and p-cresol. The ion-exchange mechanism of phenolic and indolic compound chemisorption by nanoporous carbon adsorbents, modified with surface N- and P-containing functional groups, has been proposed.

This research work provides for the possibility of cleaning soils contaminated with heavy metals with nanostructured sorbents made from plant residues. As the object of the study, soil samples from Almaty, Semey, Aktau and Ridder were taken, and the process of sorption was carried out with biosorbents made from rice husks, Pine buds and sunflower husks. Physico-chemical studies (Sam, bat, RFA) were carried out on samples prepared by carbonization of sorbents in an argon atmosphere at a temperature of 800°C. The results showed that sorbents have a high porosity and a developed surface area, which increases their adsorption capacity. According to 5-day adsorption experiments, manganese (Mn) and rubidium (Rb) were effectively sorbed with all sorbents (30-70 %). At the same time, it was shown that sunflower husks effectively absorb rubidium, Pine buds-manganese and strontium, and rice husks-iron and rubidium. The results obtained show that carbon nanosorbents from plant residues are capable of effectively cleaning soils contaminated with heavy metals and are suitable for their use as an environmentally safe physico-mechanical method.

A new iodine–dextrin–lithium complex (IDLC) was synthesized and structurally characterized as a hybrid supramolecular system combining antiseptic, stabilizing, and biocompatible components. The compound integrates iodine as the primary antimicrobial agent, lithium as a coordination and stabilization element, and dextrin as a biodegradable polysaccharide matrix enabling sustained release. Physicochemical analyses confirmed the formation of a uniform, thermally stable complex. Biological evaluation revealed strong bactericidal activity, with minimum bactericidal concentrations (MBCs) ranging from 1.95 to 15.63 µg mL⁻¹ against both Gram-positive and Gram-negative pathogens, including multidrug-resistant Staphylococcus aureus and Acinetobacter baumannii. Cytotoxicity studies revealed moderate, concentration-dependent effects on human peripheral blood mononuclear cells (CC₅₀ = 0.23–0.48 mg/mL; 11.7–24.4 μg I/mL) and low toxicity toward MDCK cells (CC₅₀ = 10–20 mg/mL; 507–1014 μg I/mL), confirming a favorable safety profile. IDLC exhibited cytotoxic effects on tumor cell lines (HepG2, HeLa, AGS, K562, and H9) as well as on the normal MeT-5A cell line; however, the CC₅₀ values are similar, and selectivity indices are close to 1, indicating no selective cytotoxicity toward tumor cells. Thus, IDLC demonstrates non-specific cytotoxicity at high concentrations, consistent with its iodine content. The research confirms that iodine can be effectively stabilized within a dextrin-lithium framework to yield a biologically active, thermally resistant complex, suitable for pharmaceutical use.