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  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Structural and Sorption Characteristics of Nano-Structured Polysaccharide Biopolymers Derived from Plants of the Asteraceae Family
    This study investigates the structural and sorption characteristics of nanostructured polysaccharide biopolymers isolated from plants of the Asteraceae family (Dahlia tubers and Helianthus tuberosus) toward Pb2+ ions in model aqueous solutions. The biopolymers were obtained by acid extraction at pH 1.5-2.5 and 80-90 °C, followed by ethanol precipitation, with a yield of 10-14%.Surface morphology examined by scanning electron microscopy revealed a hierarchically organized nano- and micro structured matrix with particle agglomeration and developed interaggregate porosity. The presence of lamellar structures and a porous network promotes diffusion of metal ions to active functional centers.The interaction mechanism between the biopolymer matrix and Pb2+ was studied by FTIR spectroscopy. Shifts and intensity changes of absorption bands corresponding to carboxyl and hydroxyl groups confirmed a coordination-chelate complexation mechanism without destruction of the polysaccharide backbone.Sorption experiments were performed using model Pb2+ solutions prepared from analytical-grade lead (II) acetate. The residual Pb2+ concentration after contact with the biopolymer was determined by atomic absorption spectrometry at 283.3 nm using calibration. Additional control measurements were conducted by complexometric titration in acetate buffer medium (pH 5.5) with 0.01 M Trilon B.Up to 76-77% of Pb2+ was removed within the first 10 min, and sorption equilibrium was reached after 60 min. The maximum removal efficiency reached 87%. The Freundlich model best described the process, indicating heterogeneous surface structure and multilayer adsorption. These results demonstrate the potential of Asteraceae-derived polysaccharide biopolymers as environmentally safe sorbents for heavy metal removal from aqueous media.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Адсорбция препарата «Вольтарен» на пористых углеродных материалах в статических и динамических условиях
    (2026-04-06)
    Jakpar Jandosov
    ;
    Alzhan Baimenov
    ;
    ;
    Е.О. Досжанов
    ;
    D. Chenchik
    The article investigates the adsorption of diclofenac (pure API and as part of the Voltaren preparation) on porous carbon materials obtained from rice husks by chemical activation methods (H3PO4, K2CO3, KOH), as well as on synthetic carbon from xerogel. A comparative assessment of the sorption capacity and the kinetics of the process was carried out under static and dynamic conditions. It was found that the KOH-activated sample (SBET = 2610 m2/g) has the highest microporosity and demonstrates the maximum adsorption capacity (up to 956 mg/g in static and up to 1016 mg/g in a column with a fixed layer). Kinetic data is well described by a pseudo second-order model (R2 > 0.99), and dynamic adsorption is described by the Thomas model (R2 = 0.998). This allows us to predict the efficiency of sorbents in flow systems. There was no significant effect of the auxiliary components of the dosage form on the sorption process. The established patterns indicate the predominant interaction of the diclofenac molecule with the microporous carbon matrix through π–π interactions and electrostatic effects. The results obtained confirm the prospects of alkaline-activated carbon materials based on biomass for the development of effective enterosorbents for intoxication with nonsteroidal anti-inflammatory drugs.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    One-stage synthesis of 1,1-diethoxyethane from ethanol using copper-containing catalysts
    (2021-10-12) ;
    Kusman Dossumov
    ;
    G.E. Ergaziyeva
    ;
    Moldir Anissova
    ;
    Bedelzhan B. Baizhomartov
    The conversion of ethanol on low-percentage copper-containing catalysts at temperatures of 300 oC and 350 oC was studied. γ-Al2O3, SiO2 and HZSM-5 were studied as the carrier of the active phase. It is shown that the main direction of ethanol conversion on low percentage copper-containing catalysts is its dehydrogenation and subsequent conversion of the resulting products into 1,1-diethoxyethane. Among the studied catalysts (1 wt.% CuO/Al2O3, 1 wt.% CuO/SiO2 and 1 wt.% CuO/ HZSM-5 the most active in the production of 1,1-diethoxyethane was 1 wt.% CuO/Al2O3, modification of it with cerium oxide led to an increase in its activity in the formation of 1,1-diethoxyethane, at the reaction temperature of 350 oС, the yield of the target product was 27 vol.%. The results showed that the modification of CuO/Al2O3 leads to an increase in the catalytic activity of the sample.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Conversion of bioethanol over oxide catalysts
    (2019-01-24)
    Gaukhar Yergaziyeva
    ;
    Samal Tayrabekova
    ;
    ; ;
    S. Smagulova
    The conversion of bioethanol over supported oxide catalysts (CuO, ZnO, Cr2O3, CeO2) was studied, among which the most active in the production of hydrogen is 3% CuO/γ-Al2O3. Modification of 3% CuO/γ-Al2O3 catalyst with Cr2O3, ZnO and CeO2 promotes the growth of hydrogen yield. The highest concentration of hydrogen at 300° C and a space velocity of 1 h-1 on CuO-ZnO / γ-Al2O3 was 48% by volume. The acidity of catalysts for adsorption-desorption of pyridine by infrared spectroscopy (ITI Matson FTIR) was determined. When the content of CuO in the catalyst is increased from 1 to 3%, the amount of Lewis acidic centers (LAS) increases from 58 to 82 μmol/gcat. Modification with chromium oxide of the copper catalyst increases the number of LAS from 82 to 156 μmol/gcat by adsorption of pyridine at 150° C and from 79 to 120 μmol/gcat with pyridine adsorption at 250 °C. It has been established that an increase in the number of Lewis acid sites has a positive effect on the yield of hydrogen in the conversion of bioethanol. According to electron microscopy, the modification of catalysts leads to an increase in the dispersity of the catalyst and to a uniform distribution of particles on the surface of the catalyst, which also contributes to its greater activity in the production of hydrogen.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Combined-Method Synthesis of CaTiO3 and SrTiO3 Perovskites with n-Hexane: Impact on Structure and Microstructure
    (2026-07-17) ; ; ; ;
    K. Ramachandran
    This study reports the synthesis of CaTiO3 and SrTiO3 with a perovskite structure by a combined route involving preliminary wet mixing of CaCO3/SrCO3 carbonates and TiO2 in n-hexane, followed by a solid – state reaction during high-temperature calcination. The phase composition and crystal structure of the obtained materials were examined by X-ray diffraction with Rietveld refinement, while the microstructure and elemental distribution were studied using SEM\EDX, and local structure and surface groups were probed by ATR– FTIR spectroscopy. It is shown that the presence of the organic solvent and the applied thermal treatment lead to the formation of single-phase CaTiO3 and SrTiO3 with orthorhombic and cubic modifications, respectively, and with crystallographic parameters with reference PDF cards. The average crystallite size calculated using the Sherrer equation confirmed the nanocrystalline nature of the powders, whereas SEM/EDX analysis reveals a highly porous microstructure and a homogeneous elemental distribution without noticeable metallic impurities. It is established that A-site cation substitution Ca2+/Sr2+ in combination with n-hexane wet mixing induces systematic changes in lattice symmetry, IR band positions and agglomerate morphology, enabling targeted tuning of the texture and potential functional properties of perovskite titanates. The proposed combined approach is a technologically simple and scalable method for producing nanostructured oxide perovskites that are promising as supports and active phases in catalytic systems for combustion processes, plasma-chemical oxidation and functional ceramics.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Биошикізат негізіндегі кеуекті көміртекті сорбциялық материалдар алу және физика-химиялық қасиеттерін зерттеу
    (2026-04-06)
    А.Р. Керимкулова
    ;
    Е.Ж. Ермолданов
    ;
    Н.М. Асанбек
    ;
    ;
    А.Н. Жумагалиева
    For the first time, an approach to the production of highly efficient porous carbon sorption materials based on lignocellulose agricultural waste has been developed and a comprehensive assessment of their physico-chemical properties has been carried out. Rice husks (RH), walnut shells (WSh), wheat straw (WSt) and pine sawdust (PS) were used as raw materials. The resulting carbonysates were chemically activated with potassium hydroxide at different mass ratios of the activating agent and the carbon matrix. To increase the surface chemical activity of sorbents, potassium hydroxide was used. The morphology of the surface and the elemental composition of the synthesized materials were studied using scanning electron microscopy and energy dispersion analysis, and the functional groups were studied using Fourier transform infrared spectroscopy (FTIR). It has been established that an increase in the degree of activation leads to the development of a hierarchical porous structure with the formation of micro-, meso- and macropores, as well as to an increase in the content of oxygen- and nitrogen-containing functional groups on the surface of carbon materials. The greatest microporosity was achieved with a KOH:carbon mass ratio of 1:4. The formed functional structure helps to increase the sorption capacity of materials in relation to toxic pollutants of various nature. The results obtained confirm the prospects of using synthesized carbon sorbents as environmentally safe and economically feasible materials for cleaning air and water environments.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Synthesis and structure of polycrystals MnCo2O4-GdCrO4
    The article discusses the synthesis and structure of polycrystalline nanocomposite MnCo2O4-GdCrO4 material. The sol-gel method was used as a synthesis of the study. Using X-ray phase analysis (XPA), the structure of the synthesized nanomaterial composition was determined: spinel – cobalt manganate and perovskite – gadolinium chromite. Based on the results of the analysis, it was established that the polycrystalline two-phase composite is a system of spinel-cubic and perovskite-tetragonal types. Morphological analysis of the nanocomposite was carried out using a scanning electron microscope (SEM). According to the data obtained as a result of SEM, the elemental composition was confirmed and the average nanosize of the nanomaterial was obtained, and the content of the compound increased to x2000 was determined, the particle size of MnCo2O4 is 383-281 nm, GdCrO4 – 1.63-1.34 µm; increased to x4000, particle size – MnCo2O4 277-219 nm, GdCrO4 – 1.48-1.27 µm; increased to x6000, particle size – MnCo2O4 239-209 nm, GdCrO4 –1.21-1.07 µm.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Получение и кинетический анализ термического разложения координационного комплекса на основе меди
    (2025-12-03)
    А. Акинжанова
    ;
    ;
    Жандос Турегулович Тауанов
    ;
    Т.Д. Махсутов
    ;
    Е. Мусатай
    This paper presents the results of the synthesis and study of the thermal decomposition of the tetraamminecopper(II) nitrate coordination complex (TACN). The morphological structure of the obtained crystals was examined using scanning electron microscopy (SEM). The crystallite sizes were analyzed with a diffractometer. The average crystallite size, calculated by the Debye-Scherrer formula for the most intense diffraction peak, was found to be 37 nm. According to thermogravimetric analysis (DTG), mass loss begins at approximately 170 °C, with the main decomposition occurring at 237 °C. Gas evolution is observed within the temperature range of 170-275 °C.
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Production and optimization of activated carbon from plant waste with high specific surface area for moisture-saving applications in agriculture
    (2024-10-20)
    Yerlan Doszhanov
    ;
    ;
    Karina Saurykova
    ;
    Zulkhair Aimukhametovich Mansurov
    ;
    In conditions of water shortage, sustainable agricultural development requires the use of water-saving technologies, including the use of water-retaining substrates based on activated carbon. In this work, the textural and adsorption characteristics of activated carbon obtained from plant waste were studied at different mass ratios of the sorbent and KOH (1:1, 1:2, 1:3 and 1:4). The aim of the study was to determine the optimal activation conditions for creating a material with a high specific surface area and a developed porous structure. The results showed that the largest pore volume (1.6 cm3/g) and a high degree of microporosity are achieved at a ratio of 1:3, which is confirmed by the analysis of pore distribution using the DFT and BJH methods. FTIR spectroscopy revealed the presence of functional groups (O–H, C=O and C–O) that contribute to water conservation. The differential pore volume distribution (dv(r), cm3/Å/g) also demonstrated that at a ratio of sorbent and KOH (1:3), the sample structure optimally combines micropores and mesopores, which increases the adsorption capacity of carbon.
    Цитирования (OpenAlex) 1
  • Некоторые метрики заблокированы вашими 
    Тип записи:Публикация,
    Механохимическая обработка природного сырья и техногенных отходов для получения теплоизоляционных материалов
    (2025-10-17)
    Alua Maten
    ;
    Bakhtiyar S. Sadykov
    ;
    Aida Artykbayeva
    ;
    А.С. Әділхан
    ;
    Re-using ash-slag waste from coal-fired power plants for thermal-insulation products offers a viable route to waste valorisation and energy saving. In this work, natural diatomite and ash-slag waste were jointly mechanochemically activated for 20 min in a «NXQM-2A» centrifugal planetary mill (powder-to-ball mass ratio 1:4) and simultaneously modified with graphite. High-energy milling destroyed residual crystalline phases, increased the amorphous aluminosilicate fraction and preserved an intrinsic pore network, which lowered the thermal conductivity of the composites to 0.10-0.12 W/m·K while raising bulk density and compressive strength (diatomite: 5.6-23.2 MPa; fly ash: 10.5-37.6 MPa). Addition of 10 wt % graphite further enhanced the hydrophobicity of diatomite – reducing water uptake by about 50% produced the minimum λ-value (0.11 W/m·K) for the ash-slag system. Conversely, 20 wt% graphite generated excessive macroporosity, lowering strength to 4-2 MPa and diminishing moisture resistance. Thus, mechanochemical activation combined with moderate graphite dosing markedly improves the thermal (lower λ) and mechanical (higher strength) performance of diatomite- and ash-based composites while simultaneously decreasing water absorption. The results confirm the feasibility of upcycling ash-slag waste into high-efficiency insulation materials suitable for building envelopes and other thermal-barrier applications.