Valorization of sponge iron industrial waste into iron-modified zeolite X for ciprofloxacin removal: a multi-parameter optimization study.

Ciprofloxacin (CIP), a commonly used antibiotic, is frequently detected in water bodies and the natural environment. The profound health consequences of CIP have led to growing attention focusing on environmental concerns. Adsorption is highly preferred because of its adaptability and remarkable efficiency in removing CIP. Therefore, the current work focuses on synthesizing an eco-friendly and economical adsorbent for removing CIP. The work aims to remove CIP using zeolite X (ZX), synthesized from dolochar, and subsequently modified ZX into iron-modified zeolite X (FeZX) via ion exchange. The synthesized FeZX had a crystallinity of 82.701%, an average pore size of 5.917 nm, a micropore volume of 0.298 cc/g, a micropore area of 451.807 m2/g, and a total surface area of 478.521 m2/g. The effect of parameters such as initial CIP concentration, pH, contact period, adsorbent dosage, and iron dosage was analyzed in the batch adsorption studies of CIP using ZX and FeZX. CIP removal of 37.786% was achieved using ZX; hence, the adsorption parameters were optimized to maximize the CIP removal using response surface methodology (RSM), specifically Box-Behnken Design (BBD) using FeZX. Maximum removal of 97.974% was achieved under optimum conditions of 8.06 pH, contact period of 59.422 min, CIP concentration of 17.117 mg/L, and adsorbent dosage of 0.478 g/L. Freundlich isotherm and pseudo-second-order kinetic models were the most accurate representations of the experimental data. The findings indicate the significance of using this iron-modified mesoporous zeolite as an adsorbent for efficiently treating CIP wastewater.

Novel chitosan-zeolite X composite beads prepared by phase-inversion method for CO2 adsorptive capture.

The urgent need to mitigate carbon emissions from industrial heat production has led to the exploration of novel carbon-based materials for carbon capture. Chitosan, a versatile framework, has been widely utilized for embedding many materials such as grafted graphene oxide, zeolite, and activated carbon to enhance the carbon capture capacity of diverse carbon-based materials. Remarkably, the combination of chitosan and zeolite overcomes the inherent drawbacks of powdery zeolite, resulting in improved stability and efficiency in carbon capture applications. In this study, zeolite X-chitosan composite was successfully synthesized using phase inversion method followed by solvent exchange and air drying. The synthesis procedure described in this study presents a notable advantage in terms of simplicity and ease of fabrication. The combination of SEM and XRD analyses provided evidence that the composite exhibited a uniform arrangement of zeolite within the chitosan framework and maintained the original properties of the powdered zeolite. The adsorption capacity of the composite was first investigated by varying mass ratio of zeolite per chitosan. The composite with mass ratio that gave the best adsorption capacity were then tested under various temperatures (-20 °C, 0 °C, 30 °C, and 50 °C) and pressures (1 kPa, 3 kPa, 5 kPa, and 30 kPa). The application of different adsorption models was also employed to simulate the breakthrough curves. Furthermore, the material also underwent multiple continuous adsorption-desorption cycles showing its potential for repeated rechargeability. In contrast, the synthesis and characterization of copper ion-exchanged composite yielded significant drop in adsorption capacity, likely due to the formation of ligands or the inherent reactivity of Cu2+ ions towards hydroxide.

High-Performance Novel MoS2@Zeolite X Nanocomposite-Modified Thin-Film Nanocomposite Forward Osmosis Membranes: A Study of Desalination and Antifouling Performance.

Novel thin-film nanocomposite (TFN) membranes modified by the MoS2@Zeolite X nanocomposite were made and studied for desalination by the forward osmosis (FO) method. Herein, MoS2@Zeolite X nanocomposite (MoS2@Z) and zeolite X particles are integrated into the polyamide (PA) selective layer of the TFN membranes, separately. The aim of this study is the synthesis of nanocomposites containing hydrophilic zeolite X particles with a modified surface and pore and improvement of their effective properties on desalination and antifouling performance. For this purpose, MoS2 nanosheets with a high hydrophilicity were selected. The existence of polymer-matrix-compatible MoS2@Z inside the PA active layer caused the formation of a defect-free smooth surface with further channels within this layer that could increase the water flux and fouling resistance of the TFN membranes. The TFN-MZ2 membrane (containing 0.01 wt % MoS2@Z) showed the top desalination performance in the FO process. In contrast to the pristine thin-film composite (TFC) and TFN-Z2 membrane (containing 0.025 wt % zeolite X, the most optimal membrane among the zeolite-modified membranes), its water flux has increased by 2.6 and 1.8 times, respectively. Furthermore, in the fouling test, this optimal TFN-MZ2 membrane with a flux decrement of 19.6% revealed an ∼2.2- and 1.8-fold enhancement in antifouling tendency compared to the TFC and TFN-Z2, respectively. Also, based on the antibiofouling test, the water flux drop of 48.6% for the TFC membrane has reached 36.9% for the optimal membrane. Hence, this high-performance TFN-MZ2 membrane shows good capability for commercial employment in FO desalination application.

Effects of Cold Sintering on the Performance of Zeolite 13X as a Consolidated Adsorbent for Cesium.

Cold sintering, a novel low-temperature consolidation technique, has shown promising results in various inorganic materials. However, the application of this technique to nanoporous materials for energy and environmental fields is not yet fully understood. This study investigates the effects of cold sintering on the relative densities, compressive strengths, chemical durabilities, crystal structures, specific surface areas, and adsorption capacities of zeolites. Cold sintering at 200 °C achieved 10 to 20% greater densification than conventional high temperature (700 °C) sintering; however, the original nanoporous structure of dry cold sintered zeolite was not maintained. Introducing liquid agents during the cold sintering process resulted in reduced degradation of the SSA and increased densification. Using NaOH as the liquid agent increased the solubility of elements in zeolite, which promoted chemical mobility and achieved the highest relative density (96.7 ± 2.8%). However, soluble layers between the particles led to fragmentation, making it unsuitable for aqueous applications. Using H2O as the liquid agent resulted in a relative density of 90.4 ± 4.1% while maintaining the nanoporous properties and structural integrity of zeolite under water. The cesium adsorption capacity (19.0 ± 0.1 mg·g-1) was similar to that of conventional zeolite ion exchangers, indicating that cold sintering with H2O was an efficient, economical, and safer alternative to conventional high-temperature consolidation method. Our findings suggest that this cold sintering can be applied to other nanoporous materials, such as metal-organic frameworks and covalent organic frameworks, in separation, catalysis, and adsorption applications.

Magnetic Induction Assisted Heating Technique in Hydrothermal Zeolite Synthesis.

The magnetic induction assisted technique is an alternative heating method for hydrothermal zeolite synthesis with a higher heat-transfer rate than that of the conventional convection oil bath technique. The research demonstrates, for the first time, the application of the magnetic induction heating technique with direct surface contact for zeolite synthesis. The magnetic induction enables direct contact between the heat source and the reactor, thereby bypassing the resistance of the heating medium layer. A comparative heat-transfer analysis between the two methods shows the higher heat-transfer rate by the magnetic induction heating technique is due to (1) eight-time higher overall heat-transfer coefficient, attributed to the absence of the resistance of the heating medium layer and (2) the higher temperature difference between the heating source and the zeolite gel. Thereby, this heating technique shows promise for application in the large-scale synthesis of zeolites due to its associated efficient heat transfer. Thus, it can provide more flexibility to the synthesis method under the non-stirred condition, which can create possibilities for the successful large-scale synthesis of a broad range of zeolites.

Synthesis of nano-crystalline zeolite-A and zeolite-X from Indian coal fly ash, its characterization and performance evaluation for the removal of Cs+ and Sr2+ from simulated nuclear waste.

Phase pure zeolite-A and zeolite-X were synthesized using coal fly ash (CFA) obtained from Indian thermal power plants by employing alkali fusion method followed by hydrothermal technique. The fusion of fly ash with Na2CO3 was accomplished by heating at 800 °C/2 h by maintaining fly ash to Na2CO3 ratio at 1.2. The fused mass was found to be nepheline (Na4Al4Si4O16); and on subsequent treatment of the fused mass with 3 M NaOH under hydrothermal condition transformed to zeolite-A (Na12Al12Si12O48.27H2O) and zeolite-X (Na88Al88Si104O384.194H2O). The effluent solution from zeolite-A synthesis was utilized to prepare cancrinite. The zeolites were characterized by XRD, FTIR, TG-DTA, SEM and surface area of the powders were measured by BET technique. The specific surface area of the zeolite-A and zeolite-X were found to be 58.29 ± 0.20 and 164.34 ± 5.4 m2g-1 respectively. The TG-DTA studies showed the conversion of nano-crystalline to micro-crystalline zeolites with loss of adsorbed water. The ion exchange capacities of these nano-crystalline zeolites were evaluated by using simulated nuclear waste solutions containing Cs+or Sr2+ ions. The adsorption capacity of zeolite-A was found to be 95.74 mg/g and 54.12 mg/g respectively for Sr2+ and Cs+ions. Similarly, zeolite-X shows the adsorption capacity of 93.14 mg/g and 53.14 mg/g respectively for Sr2+ and Cs+ ions.

Removal of methylene blue from textile waste water using kaolin and zeolite-x synthesized from Ethiopian kaolin.

The wastewater generated from textile factories is linked to one of the main water pollution problems; therefore, it is important to reduce the pollutants in industrial effluents before their discharge into environment. The present study was to investigate the appropriateness zeolite-x and kaolin as effective adsorbents for removal of methylene blue from the textile wastewater. Batch adsorption experiments were carried out to assess parameters that influence the adsorption process. The prepared zeolite-x and kaolin were characterized by Fourier Transform Infrared and X-ray diffraction techniques. The results of this study showed that the particle size is 40.77 nm and 0.45 nm kaolin and zeolite-x respectively. The performance of zeolite-x adsorbent is best at the optimum pH 4 with removal efficiency of 97.77% and kaolin adsorbent at pH 6 with removal efficiency of 86.86%. The optimum contact time was obtained at 60 and 80 minutes for zeolite-x and kaolin respectively. While optimum adsorbent dosage was obtained at 0.4 and 0.6 grams with removal efficiency of 97.12% and 87.75% for the zeolite-x and kaolin adsorption experiment respectively. The confirmed square sum errors values are 1.0×10-4 and 1.0×10-3 for zeolite-x and kaolin, respectively. The Adsorption isotherms results have well fitted to Freundlich isotherm than Langmuir isotherm. The adsorption kinetics results were best fitted the pseudo second order model. The result shows that the zeolite-x has high removal efficiency than kaolin at the same operating conditions. Application of this method can be economically, environmentally, and socially feasible to address wastewater problems. Further research has to be carried out on the removal capacity of this adsorbent for organic dyes not only from the textile industry but also from leather industries and soap industries.

Quantum Dots of [Na4 Cs6 PbBr4 ]8+ , Water Stable in Zeolite X, Luminesce Sharply in the Green.

Nanocrystals (NCs) of CsPbX3 , X = Cl, Br, or I, have excellent photoluminescent properties: high quantum yield, tunable emission wavelengths (410-700 nm), and narrow emission band widths. CsPbBr3 NCs show high promise as a green-emitting material for use in wide color gamut displays. CsPbBr3 NCs have, however, not been commercialized because they are sensitive to moisture and heat. To avoid these problems, this work attempts to introduce CsPbBr3 into five zeolites. The zeolite X product, Pb,Br,H,Cs,Na-X, shows superior stability toward moisture, maintaining its initial luminescence properties after being under water for more than a month. Its structure, determined using single-crystal X-ray crystallography, shows that quantum dots (QDs) of [Na4 Cs6 PbBr4 ]8+ (not of CsPbBr3 ) have formed. They are tetrahedral PbBr4 2- ions (Pb-Br = 3.091(11) Å) surrounded by Na+ and Cs+ ions. Each fills the zeolite's supercage with its Pb2+ ion precisely at the center, a position of high symmetry. The peaks in the emission spectra of Pb,Br,H,Cs,Na-X and the CsPbBr3 NCs are both at about 520 nm. The FWHM of Pb,Br,H,Cs,Na-X, however, is narrower than any previously reported for any of the CsPbBr3 NCs, and for zeolite Y and the various mesoporous materials treated with CsPbBr3 .

A Study on Magnetic Removal of Hexavalent Chromium from Aqueous Solutions Using Magnetite/Zeolite-X Composite Particles as Adsorbing Material.

Toxic and heavy metals are considered harmful derivatives of industrial activities; they are not biodegradable and their accumulation in living organisms can become lethal. Among other heavy and toxic metals, chromium is considered hazardous, especially in the hexavalent (Cr6+) form. Numerous established studies show that exposure to Cr6+ via drinking water leads to elevated chromium levels in tissues, which may result in various forms of cancer. The purpose of this research is to synthesize magnetite/zeolite-X composite particles for the adsorption and magnetic removal of Cr6+ ions from aqueous solutions. Synthesis and characterization of such composite nanomaterials, along with an initial experimental evaluation of Cr6+ removal from water-based solution, are presented. Results show that zeolite-X is a very promising zeolite form, that when bound to magnetic nanoparticles can be used to trap and magnetically remove toxic ions from aqueous solutions.

Impact of fly ash fractionation on the zeolitization process.

Coal combustion product in the form of fly ash has been sieved and successfully utilised as a main substrate and a carrier of silicon and aluminium in a set of hydrothermal syntheses of zeolites. The final product was abundant in zeolite X phase (Faujasite framework). Raw fly ash as well as its derivatives, after being sieved (fractions: ≤ 63, 63-125, 125-180 and ≥ 180 µm), and the obtained zeolite materials were subjected to mineralogical characterisation using powder X-ray diffraction, energy-dispersive X-ray fluorescence, laser diffraction-based particle size analysis and scanning electron microscopy. The influence of fraction separation on the zeolitization process under hydrothermal synthesis was investigated. Analyses performed on the derived zeolite X samples revealed a meaningful impact of the given fly ash fraction on synthesis efficiency, chemistry, quality as well as physicochemical properties, while favouring a given morphological form of zeolite crystals. The obtained zeolites possess great potential for use in many areas of industry and environmental protection or engineering.

Copper doped zeolite composite for antimicrobial activity and heavy metal removal from waste water.

BACKGROUND: The existence of heavy metals and coliform bacteria contaminants in aquatic system of Akaki river basin, a sub city of Addis Ababa, Ethiopia has become a public concern as human population increases and land development continues. Hence, it is the right time to design treatment technologies that can handle multiple pollutants. RESULTS: In this study, we prepared a synthetic zeolites and copper doped zeolite composite adsorbents as cost effective and simple approach to simultaneously remove heavy metals and total coliforms from wastewater of Akaki river. The synthesized copper-zeolite X composite was obtained by ion exchange method of copper ions into zeolites frameworks. Iodine test, XRD, FTIR and autosorb IQ automated gas sorption analyzer were used to characterize the adsorbents. The mean concentrations of Cd, Cr, and Pb in untreated sample were 0.795, 0.654 and 0.7025 mg/L respectively. These concentrations decreased to Cd (0.005 mg/L), Cr (0.052 mg/L) and Pb (bellow detection limit, BDL) for sample treated with bare zeolite X while a further decrease in concentration of Cd (0.005 mg/L), Cr (BDL) and Pb (BDL) was observed for the sample treated with copper-zeolite composite. Zeolite X and copper-modified zeolite X showed complete elimination of total coliforms after 90 and 50 min contact time respectively. CONCLUSION: The results obtained in this study showed high antimicrobial disinfection and heavy metal removal efficiencies of the synthesized adsorbents. Furthermore, these sorbents are efficient in significantly reducing physical parameters such as electrical conductivity, turbidity, BOD and COD.

The Use of POSS-Based Nanoadditives for Cable-Grade PVC: Effects on its Thermal Stability.

Plasticized-Poly(vinyl chloride) (P-PVC) for cables and insulation requires performances related to outdoor, indoor and submarine contexts and reduction of noxious release of HCl-containing fumes in case of thermal degradation or fire. Introducing suitable nanomaterials in polymer-based nanocomposites can be an answer to this clue. In this work, an industry-compliant cable-grade P-PVC formulation was added with nanostructured materials belonging to the family of Polyhedral Oligomeric Silsesquioxane (POSS). The effects of the nanomaterials, alone and in synergy with HCl scavenging agents as zeolites and hydrotalcites, on the thermal stability and HCl evolution of P-PVC were deeply investigated by thermogravimetric analysis and reference ASTM methods. Moreover, hardness and mechanical properties were studied in order to highlight the effects of these additives in the perspective of final industrial uses. The data demonstrated relevant improvements in the thermal stability of the samples added with nanomaterials, already with concentrations of POSS down to 0.31 phr and interesting additive effects of POSS with zeolites and hydrotalcites for HCl release reduction without losing mechanical performances.

Preparation of Zeolite X by the Aluminum Residue From Coal Fly Ash for the Adsorption of Volatile Organic Compounds.

In China, coal fly ash is a large-scale solid waste generated by power plants. The high value utilization of coal fly ash has always been a hot research issue in China for these years. In this paper, the synthesis of zeolite X using aluminum residue from coal fly ash can not only realize the resource utilization of waste, but also achieve the effect of energy saving and emission reduction. Zeolite X prepared by hydrothermal synthesis method have been found to have higher purity and better crystallinity by chemical composition analysis. By comparing and analyzing the adsorption performance of zeolite X and activated carbon on volatile organic compounds, it is found that the adsorption capacity of zeolite X is higher than that of activated carbon, and it has stronger stability. This indicates that the zeolite X synthesized by this environmentally friendly and economical method has a good application prospect in adsorbing volatile organic compounds.

Nitrate reduction on surface of Pd/Sn catalysts supported by coal fly ash-derived zeolites.

In this study, we synthesized four zeolites (i.e., Zeolite-X&A9, -X&A&HS12, -X&HS15, -X&HS18) from coal fly ash (CFA), and evaluated their potential for use as support materials to fabricate novel Pd-Sn bimetallic catalysts for reactive and selective reduction of NO3- to N2. The successive transformation of zeolite (Na-A and Na-X to hydroxy sodalite (HS)) was observed with increasing crystallization time from 9 to 18 h, which resulted in different degrees of crystallinity, morphology, BET surface area, and pore volume. Compared to other monometallic and bimetallic catalysts, Pd-Sn/Zeolite-X&HS15 (crystallization time = 15 h) showed remarkable nitrate removal (100%) with the highest kinetic rate constant (k = 0.055 min-1, K' = 0.219 min-1 gcat-1, K'' = 2.922 L min-1 gPd-1) and N2 selectivity (88.1%). These results can be attributed to high surface area and stability of each of the zeolite phases (i.e., Na-X and HS). The reaction mechanism was elucidated by Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy analyses, demonstrating the presence of Pd°, Sn°, and Sn2+ and the uniform distribution of proximate Pd-Sn ensembles on the surface. These results suggest new promising strategies for applying industrial solid waste-derived zeolites to the synthesis of novel bimetallic catalysts to ensure efficient and economical denitrification of wastewater.

An ultra-fast non-conventional waste management protocol to recycle of industrial fly ash into zeolite X.

An ultra-fast non-conventional waste management protocol was being designed and applied to recycle and reuse industrial coal fly ash (CFA) waste to generate highly pure nanozeolite X. Both microwave heating-assisted hydrothermal treatment method and ultrasonic waves-assisted hydrothermal method have been successfully used for the fast valorization of power plant CFA waste, and the results were compared with conversional valorization method for CFA conversion to zeolite. While conventional methods like hydrothermal treatment using sodium hydroxide took up to 4 days in valorization of the solid CFA waste into a useful zeolitic X material; the non-conventional methods using microwave irradiation of frequency 2.45 GHz and ultrasound irradiation of frequency 20 kHz took 90 min and 20 min respectively to fast-valorize the solid waste into highly pure zeolite material with high cation-exchanged capacity. The unconventional techniques, therefore, can be used in the large-scale valorization of solid waste recycling and reuse to yield highly pure zeolite.

Selective synthesis of zeolites A and X from two industrial wastes: Crushed stone powder and aluminum ash.

Crushed stone powder and aluminum ash are industrial wastes, and effective utilization of these wastes has been highly expected. Since the main components of the two wastes are Si, Al and O, those wastes can be used as starting materials for synthesis of zeolites of which some types have been commercialized as catalysts and ion-exchangers. In this study, zeolites A and X well-known as practical materials were successfully synthesized with high purity using the two industrial wastes by a mild process based on two hydrothermal treatments with intermediate acid treatment. In the first hydrothermal treatment at 150 °C, quartz in the crushed stone powder was dissolved and acid-soluble hydroxysodalite (Na8(AlSiO4)6(H2O)2(OH)2) with Si/Al = 1 and sodium aluminosilicate (Na6(AlSiO4)6) were formed. Those compounds were dissolved with HCl aq. solution. The zeolites were successfully synthesized from the second hydrothermal treatment of the yellow dried filtrates at 80 °C in NaOH aq. solution. In the process proposed, removal of Ca from the crushed stone powder was effective to formation of zeolites A and/or X. Selective synthesis of zeolites A and X was achieved by controlling the acid treatment conditions. Furthermore, the effect of the drying condition of the filtrate obtained after the acid treatment was also investigated on the differences in the product phase.

Zeolite X from coal fly ash inhibits proliferation of human breast cancer cell lines (MCF-7) via induction of S phase arrest and apoptosis.

In this study, zeolite X synthesised from coal fly ash (CFA) was examined for its anti-proliferative effects on human breast cancer MCF-7 cells by in vitro studies and allied probable molecular mechanism were also assessed. MTT assay exposed that zeolite X showed a concentration-dependent inhibitory result on the proliferation of MCF-7 cells and caused early apoptotic death and does not induce cytotoxicity in non-cancerous cells (MCF-12A). Flow cytometric study specified the accrual of cells at S phase suggest induction of apoptosis which was avowed through fluorescence and confocal microscopy following annexin V-FITC/propidium iodide (PI). MCF-7 cells treated by 10, 15 and 20 µg/ml concentrations of zeolite X showed internucleosomal DNA fragments in ladder form, thereby indicates cell death is associated with apoptosis. Mechanistically, our data support the induction of apoptosis through the activation of mitochondrial dependent pathway as indicated by an up-regulation of Bax and downregulation of Bcl-2 ratio, the expulsion of cytochrome c from the mitochondria to the cytosol and cleavage of pro-caspase-3 into activation of caspase-3 in MCF-7 cells. Based on these outcomes zeolite X induced early apoptosis and strongly provided experimental evidence for the usage of zeolite X as an essential therapeutic agent in the prevention and therapy of human breast cancer.

Induction of apoptotic effects of anti-proliferative zeolite X from coal fly ash on cervical cancer (HeLa) cell lines.

The synthesised zeolite X from coal fly ash showed significant cytotoxic activity in contradiction of HeLa cells (cervical cancer) in a concentration-dependent way at concentrations ranges from 200 µg to 0.781 µg/ml as shown by MTT assay and failed to cause cytotoxic effect in normal cells (Gh239). Cell cycle analysis exposed that zeolite X (10 and 15 µg/ml) endorses cell growth inhibition by inducing G2/M phase arrest in HeLa cells as observed using flow cytometry. The confocal microscopic results depicted increased early apoptotic related changes in HeLa cell lines induced by zeolite X at a dosage of 10, 15 and 20 µg/ml. Zeolite X at a dosage of 10, 15 and 20 µg/ml in HeLa cells showed fragmentation of DNA by ladder pattern thereby indicates that cell death is related with apoptosis. By the increase of Bax/Bcl-2 ratio, zeolite X leads to the caspase-3 and caspase-9 activation and allow the cells to enter apoptosis. These collective results evidently showed that the influence of mitochondria-mediated signalling pathway in zeolite X induced apoptosis and intensely delivered investigational suggestion for the use of zeolite X as a significant curative agent in the preclusion and therapy of human cervical carcinoma.

One-Step Hydrothermal Synthesis of Zeolite X Powder from Natural Low-Grade Diatomite.

Zeolite X powder was synthesized using natural low-grade diatomite as the main source of Si but only as a partial source of Al via a simple and green hydrothermal method. The microstructure and surface properties of the obtained samples were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), wavelength dispersive X-ray fluorescence (XRF), calcium ion exchange capacity (CEC), thermogravimetric-differential thermal (TG-DTA) analysis, and N2 adsorption-desorption technique. The influence of various synthesis factors, including aging time and temperature, crystallization time and temperature, Na2O/SiO2 and H2O/Na2O ratio on the CEC of zeolite, were systematically investigated. The as-synthesized zeolite X with binary meso-microporous structure possessed remarkable thermal stability, high calcium ion exchange capacity of 248 mg/g and large surface area of 453 m²/g. In addition, the calcium ion exchange capacity of zeolite X was found to be mainly determined by the crystallization degree. In conclusion, the synthesized zeolite X using diatomite as a cost-effective raw material in this study has great potential for industrial application such as catalyst support and adsorbent.

Sorption of Cu(II) Ions on Chitosan-Zeolite X Composites: Impact of Gelling and Drying Conditions.

Chitosan-zeolite Na-X composite beads with open porosity and different zeolite contents were prepared by an encapsulation method. Preparation conditions had to be optimised in order to stabilize the zeolite network during the polysaccharide gelling process. Composites and pure reference components were characterized using X-ray diffraction (XRD); scanning electron microscopy (SEM); N2 adsorption-desorption; and thermogravimetric analysis (TG). Cu(II) sorption was investigated at pH 6. The choice of drying method used for the storage of the adsorbent severely affects the textural properties of the composite and the copper sorption effectiveness. The copper sorption capacity of chitosan hydrogel is about 190 mg·g(-1). More than 70% of this capacity is retained when the polysaccharide is stored as an aerogel after supercrititcal CO2 drying, but nearly 90% of the capacity is lost after evaporative drying to a xerogel. Textural data and Cu(II) sorption data indicate that the properties of the zeolite-polysaccharide composites are not just the sum of the properties of the individual components. Whereas a chitosan coating impairs the accessibility of the microporosity of the zeolite; the presence of the zeolite improves the stability of the dispersion of chitosan upon supercritical drying and increases the affinity of the composites for Cu(II) cations. Chitosan-zeolite aerogels present Cu(II) sorption properties.