In this paper, the modification of natural clinoptilolite and mordenite zeolites from Almaty using acid treatment is addressed for the purposes of improving adsorption performance and for drinking water purification. Structural chemical transformation was characterized by the use of X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Scanning electron microscope (SEM) techniques. Acid treatment led to a partial dealumination that was responsible for an increase in the number of surface defects and micropores, improvement in ion exchange capacity, and selectivity toward heavy metals. Additionally, modifications greatly enhance the uptake capacities of Pb²⁺, Cd²⁺, and As³⁺. The clinoptilolite post-modification removal efficiencies reached 94%, 86%, and 84%, respectively, while mordenite zeolites achieved 95%, 90%, and 87% removal efficiencies, respectively. The enhancement of performance was related to the increase in surface area and active sites for ion exchange, verified from analysis of the Brunauer-Emmett-Teller (BET) surface area. The use of different Bhatt and Kothari methods has revealed that adsorption processes followed Langmuir isotherm models for Pb²⁺ and Cd²⁺, whereas As³⁺ adsorption was better described by the Freundlich isotherm model. However, second-order kinetics indicate that chemisorption was the dominant mechanism. Such evidence indicates spontaneity and an endothermic process, as shown from thermodynamic studies. Results showed that modified zeolites indeed had a high degree of reusability, with over 80% of the adsorption capacity retained even after five cycles. Acid-modified zeolites can provide cheaper, greener methods of purification, generating only negligible secondary waste when compared to conventional methods of water purification, for example, activated carbon and membrane filtration. Results from this study proved that modified clinoptilolite and mordenite zeolites have the potential for sustainable heavy metal treatment in drinking water purification systems.

Potatoes (Solanum tuberosum L.) constitute one of the most economically important annual crops. In terms of tissue culture, potato microtubers (MTs) have a number of advantages over conventional plants. These advantages include their small size, which greatly facilitates storage, transport, and germplasm exchange compared to in vitro plants. One effective solution for the production and mass propagation of healthy MTs is the use of temporary immersion systems (TISs). In this study, in a SETIS^TM system containing kinetin/gibberellic acid (GA)/indole-3-butyric acid (IBA) hormones, we investigated the effects of different nutrient media on the morphological characteristics of potato explants and MTs. We determined the optimal cycling duration (3 h) with an immersion frequency of 2 min. The results revealed that the optimal nutrient medium for culturing single-node potato explants in a SETIS^TM bioreactor was the M7 medium containing kinetin (2 mg/L), GA (0.5 mg/L), and IBA (0.5 mg/L). The optimal nutrient medium for obtaining potato MTs was the M1 medium (hormone-free) with a high concentration of sucrose (9%) at 18 °C under dark growing conditions. Thus, a universal nutrient medium, employed in a bioreactor, was selected for the mass propagation of potato MTs for both domestic and foreign potato varieties.

The sustainable operation of hydroponic systems depends on maintaining the chemical stability of circulating nutrient solutions and preventing the accumulation of toxic compounds. The accumulation of phytotoxic ammonium, heavy metals, and organic metabolites in recirculating nutrient solutions remains one of the key challenges limiting the efficiency, sustainability, and scalability of hydroponic cultivation. This review provides a comprehensive comparative analysis of zeolites, activated carbons (ACs), and their functionalized and composite forms as key sorbents for nutrient management, contaminant removal, and environmental safety in hydroponic cultivation. Natural zeolites, with their well-defined crystalline structure and high ion-exchange selectivity toward ammonium and heavy metal cations, enable effective NH₄⁺/K⁺ balance regulation and phytotoxicity mitigation. ACs, characterized by high specific surface area and tunable surface chemistry, complement zeolites by offering extensive adsorption capacity for organic compounds, root exudates, and pesticide residues, thereby extending the operational lifespan of nutrient solutions and improving overall system performance. Further advancements include the integration of zeolites and ACs with two-dimensional (graphene, g-C₃N₄) and three-dimensional (MOF, COF) frameworks, yielding multifunctional materials that combine adsorption, ion exchange, photocatalysis, and nutrient regulation. Transition-metal modification, particularly with Fe, Mn, Cu, Ni, and Co, introduces redox-active centers that enhance sorption, catalysis, and phosphate stabilization. The comparative synthesis reveals that the combined application of zeolite- and carbon-based composites offers a synergistic strategy for developing adaptive and low-waste hydroponic systems. From a techno-economic and environmental standpoint, the judicious application of these materials paves the way for more resilient, efficient, and circular hydroponic systems, reducing fertilizer and water consumption, lowering contaminant discharge, and enhancing food security. This systematic review was conducted according to the PRISMA 2020 guidelines. Relevant studies were identified through Scopus, Web of Science, and Google Scholar databases using specific inclusion and exclusion criteria.

In this paper the modification of natural clinoptilolite and mordenite zeolites from Almaty using acid treatment is addressed for the purposes of improving adsorption performance and for drinking water purification. Structural chemical transformation was characterized by the use of XRD, FTIR, and SEM techniques. Acid treatment led to a partial dealumination that was responsible for the increase in number of surface defects and micropores, improvement in ion exchange capacity and selectivity toward heavy metals. Additionally, modifications greatly enhance the uptake capacities of Pb²⁺, Cd²⁺ and As³⁺. The clinoptilolite post-modification removal efficiencies reached 94%, 86%, and 84% respectively, while mordenite zeolites achieved 95%, 90%, and 87% removal efficiencies respectively. The enhancement of performance was related to the increase of surface area and active sites for ion exchange, verified from analysis of BET surface area. The use of different Bhatt and Kothari methods has revealed that adsorption processes followed Langmuir isotherm models for Pb²⁺ and Cd²⁺, whereas As³⁺ adsorption was better described by the Freundlich isotherm model. However, second-order kinetics indicate that chemisorption was the dominant mechanism. Such evidence indicates spontaneity and an endothermic process, as shown from thermodynamic studies. Results showed that modified zeolites indeed had a high degree of reusability, with over 80% of the adsorption capacity retained even after five cycles. Acid-modified zeolites can provide cheaper, greener methods of purification, generating only negligible secondary waste when compare to conventional methods of water purification, for example, activated carbon and membrane filtration. Results from this study proved that modified clinoptilolite and mordenite zeolites have the potential for sustainable heavy metal treatment in drinking water purification systems.

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.

Устойчивое развитие сельского хозяйства в условиях глобального изменения климата и ограниченных водных ресурсов требует внедрения инновационных материалов с повышенной влагоудерживающей способностью, включая углеродные субстраты на основе сельскохозяйственных отходов. В данной работе проведено комплексное исследование текстурных, морфологических и адсорбционных характеристик активированного угля (АУ), синтезированного из рисовой шелухи при варьировании массовых соотношений сорбента к гидроксиду калия (KOH) (1:1, 1:2, 1:3 и 1:4). Цель работы – оптимизация условий химической активации для формирования пористой структуры, обеспечивающей эффективное влагоудержание. Методология включала применение теории функционала плотности (DFT) и метода Барретта–Джойнера–Халенды (BJH). Результаты показали, что максимальный суммарный объем пор (1,6 см3/г) и развитая удельная поверхность (2900 м2/г) достигаются при соотношении 1:3. ИК-Фурье спектроскопия подтвердила наличие гидрофильных функциональных групп (O-H, C=O, C-O), играющих ключевую роль в связывании молекул воды. Эксперименты по влагоудержанию, выполненные в трехкратной повторности (n=3), продемонстрировали, что образец 1:3 характеризуется наиболее стабильным сохранением влаги как при 22 ºC, так и при повышенной температуре 50 ºC, значительно превосходя образцы с низкой степенью активации (1:1, 1:2) и переактивированный образец (1:4). Сравнительный анализ показал, что оптимизированный АУ обладает превосходством над традиционным биоуглем и цеолитами по удельной поверхности, обеспечивая долгосрочную стабильность углеродного каркаса в почве. Полученные данные подтверждают ключевую роль баланса микро- и мезопор в процессах замедления испарения воды и свидетельствуют о высокой перспективности использования данных материалов в качестве экологически безопасных влагосберегающих агентов для повышения продуктивности агроценозов в засушливых регионах.