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Given that methane (CH₄) and nitrogen (N₂) have similar properties, achieving high-purity enrichment of CH₄ from nitrogen-rich low-grade gas is extremely challenging and is of great significance for sustainable development in energy and the environment. This paper reviews the research progress on carbon-based materials, zeolites, and MOFs as adsorbent materials for CH₄/N₂ separation. It focuses on the relationship between the composition, pore size, surface chemistry of the adsorbents, CH₄/N₂ selectivity, and CH₄ adsorption capacity. The paper also highlights that controlling pore size and atomic-scale composition and optimizing these features for the best match are key directions for the development of new adsorbents. Additionally, it points out that MOFs, which combine the advantages of carbon-based adsorbents and zeolites, are likely to become the most promising adsorbent materials for efficient CH₄/N₂ separation. Full article

The present work deals with the hydrothermal synthesis of a Na-A (LTA) zeolite using rice husk as a starting material. The focus was on defining the most favorable conditions for the synthesis of zeolite Na-A from rice husk in order to economize on both energy (i.e., synthesis temperatures) and reaction time and to enlarge the field of the pure and isolated synthesized phase. Four sets of experiments were carried out at environmental pressure temperatures varying from 40 °C to 85 °C with a SiO₂/Al₂O₃ ratio from 1.75 to 3.5. Optimal conditions for crystallization of the Na-A zeolite from rice husk were reached at 60 °C with a SiO₂/Al₂O₃ ratio of 1.75. Sixty degrees Celsius represents the minimum known temperature used for the synthesis of NaA zeolite from rice husk. The products of synthesis were characterized by X-ray diffraction, scanning electron microscopy, infrared and Raman spectroscopy. The purity of the synthesized zeolite is verified here for the first time through quantitative phase analysis using the combined Rietveld and reference intensity ratio methods. Full article

In oxygen production on plateaus, pressure swing adsorption (PSA) oxygen production is currently the most commonly used oxygen production method. In plateau regions, low pressure leads to a decrease in adsorbent nitrogen–oxygen separation performance, which affects the performance of PSA oxygen production, so it is particularly important to enhance adsorbent nitrogen–oxygen separation performance. In this paper, Li-LSX (lithium low-silicon aluminum X zeolite molecular sieve) adsorbents were modified using the liquid phase ion exchange method, and five kinds of modified adsorbents were obtained, namely AgLi-LSX, CaLi-LSX, ZnLi-LSX, CuLi-LSX, and FeLi-LSX, respectively. The influences of different metal ions and modification time lengths on the adsorbent nitrogen adsorption and nitrogen–oxygen separation coefficients were analyzed. Through theoretical calculations, the nitrogen and oxygen adsorption and separation performances of the modified adsorbents at different altitudes and low adsorption pressures were investigated. It is shown that the nitrogen adsorption capacity of the AgLi-LSX-1 adsorbent obtained from the modification experiment reaches 27.92 mL/g, which is 3.24 mL/g higher than that of Li-LSX; the nitrogen–oxygen separation coefficients of S1 and S2 are 19.24 and 7.54 higher, respectively; and the nitrogen–oxygen separation coefficients of S4 are 20.85 and 7.54 higher than those of Li-LSX, respectively. With the increase in altitude from 50 m to 5000 m, the nitrogen–oxygen separation coefficient of the AgLi-LSX-1 adsorbent increased rapidly from 20.85 to 57, and its nitrogen–oxygen separation coefficient S4 exceeded that of the Li-LSX adsorbent to reach 47.61 at an altitude of 4000 m. Therefore, the modified adsorbent AgLi-LSX-1 in this paper can enhance the performance of the PSA oxygen process for oxygen production in plateau applications. Full article

Although soil stabilization with cement and lime is widely used to overcome the low shear strength of soft clay, which can cause severe damage to the infrastructures founded on such soils, such binders have severe impacts on the environment in terms of increasing emissions of carbon dioxide and the consumption of energy. Therefore, it is necessary to investigate soil improvement using sustainable materials such as byproducts or natural resources as alternatives to conventional binders—cement and lime. In this study, the combination of cement kiln dust as a byproduct and zeolite was used to produce an alkali-activated matrix. The results showed that the strength increased from 124 kPa for the untreated clay to 572 kPa for clay treated with 30% activated stabilizer agent (activated cement kiln dust). Moreover, incorporating zeolite as a partial replacement of the activated cement kiln dust increased the strength drastically to 960 and 2530 kPa for zeolite ratios of 0.1 and 0.6, respectively, which then decreased sharply to 1167 and 800 kPa with further increasing zeolite/pr to 0.8 and 1.0, respectively. The soil that was improved with the activated stabilizer agents was tested under footings subjected to eccentric loading. The results of large-scale loading tests showed clear improvements in terms of increasing the bearing capacity and decreasing the tilt of the footings. Also, a reduction occurred due to the eccentricity decreasing as a result of increasing the thickness of the treated soil layer beneath the footing. Full article

Ammonium ion is a chemical species that is found in abundance in natural waters, whether underground or surface, but also in wastewater resulting from agricultural and industrial activities. Even if the removal of the ammonium ion from water has been studied for a very long time, it has been found that its removal is far from being solved. In this study, we evaluated the performance of the ammonium ion adsorption process on two adsorbents, zeolite clinoptilolite, ZR, a sustainable material (manufacturer: Zeolite Development SRL, Rupea, Brasov, Romania), and the other granular activated carbon type, Norit GAC 830 W. Zeolite ZR is found in very large deposits in Romania; it is a natural, cheap material with costs between 50 and 100 EUR/ton, compared to other adsorbents that cost over 500 EUR/ton and which can be regenerated and reused in the technological process of water treatment and purification, but also after exhaustion, as an amendment for the soil. In the first step, this paper presents the mineralogic (XRD) and structural (SEM and EDX) characterization of the ZR and the determination of the pH zero-point charge, pH_ZPC, for all the adsorbents. Studies were carried out in equilibrium and kinetic conditions. The efficiency of the adsorbent was investigated in different experimental conditions by varying the initial concentration, particle size, temperature, pH, ionic strength, and contact time. The mathematical models and parameters specific to the adsorption isotherms that best describe the experimental results were identified. Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich mathematical models were used for comparison. The Langmuir isotherm proved to be the most appropriate to describe the adsorption of ammonium ions on all types of adsorbents used. The adsorption capacity of ammonium ions from synthetic solutions at 20 °C, pH = 6.09, for the range of initial concentrations 0–50 mg/L for Rupea zeolite is in the range of 10.46 mg/g−12.34 mg/g, and for granular activated carbon GAC W830, it is 16.64 mg/g. It was found that the adsorption capacity of the ammonium ion on both activated carbon and zeolite increases with increasing temperature and pH. Also, it was observed that as the ionic strength increases, the adsorption capacity decreases for all four adsorbents. Kinetic models were also identified that best describe the experimental processes. In this sense, pseudo-first order, pseudo-second order, intra-particle diffusion and the Elovich model were used. The results of the investigation showed that second-order kinetics governs the adsorption process on ZR, and pseudo-first order governs activated carbon. Full article

The release of Neogene volcanism in the southeastern part of the Iberian Peninsula produced a series of volcanic structures in the form of stratovolcanoes and calderas; however, other materials also accumulated such as large amounts of pyroclastic materials such as cinerites, ashes, and lapilli, which were later altered to form deposits of zeolites and bentonites. This work has focused on an area located on the northern flank of the San José-Los Escullos zeolite deposit, the only one of its kind with industrial capacity in Spain. The main objective of this research is to characterize the zeolite (SZ) of this new area from the mineral, chemical, and technical points of view and establish its possible use as a natural pozzolan. In the first stage, a study of the mineralogical and chemical composition of the selected samples was carried out using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray fluorescence (XRF), and thermogravimetric analysis (TGA); in the second stage, chemical-qualitative and pozzolanicity technical tests were carried out at 8 and 15 days. In addition, a chemical analysis was performed using XRF on the specimens of mortars made with a standardized mixture of Portland cement (PC: 75%) and natural zeolite (SZ: 25%) at the ages of 7, 28, and 90 days. The results of the mineralogical analyses indicated that the samples are made up mainly of mordenite and subordinately by smectite, plagioclase, quartz, halloysite, illite, and muscovite. Qualitative chemical assays indicated a high percentage of reactive silica and reactive CaO and also negligible contents of insoluble residues. The results of the pozzolanicity test indicate that all the samples analyzed behave like natural pozzolans of good quality, increasing their pozzolanic reactivity from 8 to 15 days of testing. Chemical analyses of PC/SZ composite mortar specimens showed how a significant part of SiO₂ and Al₂O₃ are released by zeolite while it absorbs a large part of the SO₃ contained in the cement. The results presented in this research could be of great practical and scientific importance as they indicate the continuation of zeolitic mineralization beyond the limits of the San José-Los Escullos deposit, which would result in an increase in geological reserves and the extension of the useful life of the deposit, which is of vital importance to the local mining industry. Full article

Nanofibre-based membranes have shown great potential for removing textile wastewater due to their high porosity and surface area. However, nanofibre membranes exhibit lower dye removal efficiency. Hence, this study aims to improve the dye removal performance of nanofibre membranes by incorporating zeolites. The research involved fabricating composite membranes by electrospinning polyvinyl alcohol (PVA) nanofibres incorporated with zeolites. Mechanical strength was enhanced by placing the PVA/zeolite nanofibre membrane between fusible nonwoven interfacing and woven polyester fabric, followed by heat treatment. Morphological analysis revealed the uniform dispersion of zeolite particles within the PVA nanofibres. EDX analysis confirmed the successful incorporation of zeolites into the fibres. Among all membrane samples, the PZ-0.75 membrane exhibited the highest pure water flux (PWF) with approximately 1358.57 L·m⁻²·min⁻¹ for distilled water and 499.85 L·m⁻²·min⁻¹ for batik wastewater. Turbidity of batik wastewater increased proportionally with zeolite concentration, with removal rates of 84.79%, 78.8%, 76.96%, and 74.19% for PZ-0.75, PZ-0.5, PZ-0.25, and PVA membranes, respectively. Furthermore, the UV/Vis spectrophotometer demonstrated that dye removal efficiency increased from 2.22% to 8.89% as the zeolite concentration increased from 0% to 0.75%. In addition, the PZ-0.75 membrane effectively removed RR dye at a concentration of 1 mg/L, with an optimal contact time of approximately 60 min. The adsorption mechanism of the PZ-0.75 membrane aligns with the Freundlich model, with an R² value of 0.983. Overall, this study demonstrates the efficiency of zeolite in the fabric substrates to improve the filtration and adsorption properties for wastewater treatment, particularly in textile industries. Full article

Plastic pollution is a critical environmental issue due to the widespread use of plastic materials and their long degradation time. Hydrocracking (HDC) offers a promising solution to manage plastic waste by converting it into valuable products, namely chemicals or fuels. This work aims to investigates the effect of catalyst accessibility and acidity on the HDC reaction of high density polyethylene (HDPE). Therefore, a variety of materials with significant differences in both textural and acidic properties were tested as catalysts. These include H-USY and H-ZSM.5 zeolites with various Si/Al molar ratios (H-USY: Si/Al = 2.9, 15, 30 and 40; H-ZSM-5: Si/Al = 11.5, 40, 500) and mesostructured MCM-41 materials modified with Ga and Al, also with different Si/metal ratios (Si/Al = 16 and 30; Si/Ga = 63 and 82). Thermogravimetric analysis under hydrogen atmosphere was used as a preliminary screening tool to evaluate the potential of the various catalysts for this application in terms of energy requirements. In addition, batch autoclave reactor experiments (T = 300 °C, PH₂ = 20 bar, t = 60 min) were conducted to obtain further information on conversion, product yields and product distribution for the most promising systems. The results show that the catalytic performance in HDPE hydrocracking is determined by a balance between the acidity of the catalyst and its structural accessibility. Accordingly, for catalyst series where the structural and textural properties do not vary with the Si/Al ratio, there is a clear correlation of the HDPE degradation temperature and of the HDPE conversion with the Si/metal ratio (which relates to the acidic properties). In contrast, for catalyst series where the structural and textural properties vary with the Si/Al ratio, no consistent trend is observed and the catalytic performance is determined by a balance between the acidic and textural properties. The product distribution was also found to be influenced by the physical and chemical properties of the catalyst. Catalysts with strong acidity and smaller pores were observed to favor the formation of lighter hydrocarbons. In addition to the textural and acidic properties of the catalyst, the role of coke formation should not be neglected to ensure a comprehensive analysis of the catalytic performance. Full article

Black-odor water, which is caused by the excessive accumulation of nitrogen and phosphorus in water, is a significant problem. Immobilized microorganisms are considered to be an effective technical solution, but there are still many key parameters to be determined, such as organic matter dissolution, insufficient stability, and insufficient phosphorus removal capacity, among other problems. In this study, the optimum raw material ratios of immobilized microorganism gel beads were determined by means of a response surface experiment. The optimal ratio of raw materials was 5% polyvinyl alcohol (PVA), 1% sodium alginate (SA), and 6% bacterial powder. In addition, the nitrogen and phosphorus removal performance of the materials was improved by loading inorganic compounds, such as 0.5 wt.% zeolite, 0.5 wt.% iron powder, and 0.2 wt.% activated carbon. Tolerance analysis determined that these gel beads could maintain a good performance in a series of harsh environments, such as during intense agitation, at high temperatures, and at low pH values, etc. The total nitrogen (TN), ammonia nitrogen (NH₃-N), and phosphorus (TP) removal efficiencies were 88.9%, 90%, and 95%. Full article

Diffusional limitations associated with zeolite microporous systems can be overcome by developing hierarchical zeolites, i.e., materials with a micro- and mesoporous framework. In this work, Y and ZSM-5 zeolites were modified using a surfactant-mediated hydrothermal alkaline method, with NaOH and cetyltrimethylammonium bromide (CTAB). For Y zeolite, after a mild acidic pretreatment, the effect of the NaOH+CTAB treatment time was investigated. For ZSM-5 zeolite, different concentrations of the base and acid solutions were tested in the two-step pretreatment preceding the hydrothermal treatment. The properties of the materials were studied with different physical–chemical techniques. Hierarchical Y zeolites were characterized by 3.3–5 nm pores formed during the alkaline treatment through the structure reconstruction around the surfactant aggregates. The effectiveness of the NaOH+CTAB treatment was highly dependent on the duration. For intermediate treatment times (6–12 h), both smaller and larger mesopores were also obtained. Hierarchical ZSM-5 zeolites showed a disordered mesoporosity, mainly resulting from the pretreatment rather than from the subsequent hydrothermal treatment. High mesoporosity was obtained when the concentration of the pretreating base solution was sufficiently high and that of the acid one was not excessive. Hierarchical materials can be obtained for both zeolite structures, but the pretreatment and treatment conditions must be tailored to the starting zeolite and the desired type of mesoporosity. Full article

It is imperative to eliminate heavy metals and pharmaceutical residual pollutants from wastewater to reduce their detrimental effects on the environment. In this work, natural zeolite and a 2-amino terephthalic acid-based multi-metallic organic framework were used to create a new composite that can be utilized as an adsorbent for cadmium and safinamide. The adsorption study was examined in a variety of settings (pH, adsorbent dosage, pollutant concentration, and time). Moreover, Zeta potential, BET, SEM, FTIR, XRD, and SEM measurements were used to characterize the adsorbents. The adsorption process was confirmed using FTIR, XRD, and SEM analysis. Various nonlinear adsorption isotherm models were applied to adsorption results. The results showed a significantly better adsorption ability for safinamide and cadmium using zeolite/MOF compared to zeolite. Adsorption kinetics were represented by five models: pseudo first-order, pseudo second-order, intraparticle diffusion, mixed first- and second-order, and the Avrami model. Regarding both adsorbent substances, safinamide adsorption was best represented by the intraparticle diffusion model. In contrast, the pseudo second-order and intraparticle diffusion models for zeolite and zeolite/MOF, respectively, better fit the experimental results in the case of cadmium adsorption. The thermodynamic parameters ΔH°, ΔS°, and ΔG° were investigated through temperature tests carried out at 25, 35, 45, and 55 °C. Exothermic and spontaneous adsorption processes were demonstrated by the computed values. The study of adsorbent regeneration involved the use of several chemical solvents. The DMSO solvent was shown to have the highest adsorbent regeneration method efficiency at 63%. Safinamide elimination was lessened by organic interfering species like cefixime and humic acid compared to inorganic species like chloride, sulphate, and nitrate, most likely as a result of intense competition for the few available active sites. Using zeolite/MOF nanocomposite, the percentage of safinamide removed from spiked real water samples (tap water, Nile River water, and groundwater samples) was 48.80%, 64.30%, and 44.44%, respectively. Based on cytotoxicity results, the highest percentages of cell viability for zeolite and zeolite/MOF at 24 h were 83% and 81%, respectively, in comparison to untreated controls. According to these results, zeolite and zeolite/MOF composites can be used as effective adsorbents for these pollutants in wastewater. Full article

In porous water filters, the transport and entrapment of contaminants can be modeled as a classic mass transport problem, which employs the conventional convection–dispersion equation to predict the transport of species existing in trace amounts. Using the volume-averaging method (VAM), the upscaling has revealed two possible macroscopic equations for predicting contaminant concentrations in the filters. The first equation is the classical convection–dispersion equation, which incorporates a total dispersion tensor. The second equation involves an additional transport coefficient, identified as the adsorption-induced vector. In this study, the aforementioned equations were solved in 1D for column tests using 3D unit cells. The simulated breakthrough curves (BTCs), using the proposed micro–macro-coupling-based VAM model, are compared with the direct numerical simulation (DNS) results based on BCC-type unit cells arranged one-after-another in a daisy chain manner, as well as with three previously reported experimental works, in which the functionalized zeolite and zero-valent iron fillings were used as an adsorbent to remove phosphorous and arsenic from water, respectively. The disagreement of VAM BTC predictions with DNS and experimental results reveals the need for an alternative closure formulation in VAM. Detailed investigations reveal time constraint violations in all the three cases, suggesting this as the main cause of VAM’s failure. Full article

We herein report successful syntheses of both nickel cobalt sulfide (NCS) and its composite with zeolite (NCS@Z) using a solvothermal method. Techniques such as EDX analysis, SEM, and molar ratio determination were used for product characterization. The incorporation of NCS significantly changed the surface roughness and active sites of the zeolite, improving the efficiency of methylene blue degradation and its reusability, especially under UV irradiation. In comparing the pseudo-first order rates, the highest degradation efficiency of methylene blue was achieved with NCS-2@Z, having a degradation extent of 91.07% under UV irradiation. This environmentally friendly approach offers a promising solution for the remediation of methylene blue contamination in various industries. Full article

A versatile building material, foamed concrete is made of cement, fine aggregate, and foam combined with coarse aggregate. This study provides a description of how constant coarse aggregate replacement (50%) of LECA and foamed concrete, which are lightweight concrete types, by zeolite as a filler and PEG-400 as a plasticizer, water retention agent, and strength enhancer affect the mechanical properties of the cement. A study that examined the characteristics of cellular lightweight concrete in both its fresh and hardened forms was carried out for both foamed concrete and LECA concrete. In order to do this, a composite of zeolite and polyethylene glycol 400 was made using the direct absorption method, and no leakage was seen. Zeolite was loaded to a level of 10% and 20% of the total weight in cement, while 400 g/mol PEG was used at levels of 1%, 1.5%, and 2% of the cement’s weight. Various mixtures having a dry density of 1250 kg/m³ were produced. Properties like dry density, splitting tensile strength, and compressive strength were measured. An increase in the amount of PEG400–zeolite was seen to lower the workability, or slump, of both foamed and LECA concrete, while the replacement of aggregate by zeolite resulted in an exponential drop in both compressive and flexural strengths. Full article