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Keywords = synthetic analcime

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15 pages, 5316 KiB  
Article
Sea Sand as a Silica Source to Hydrothermally Synthesize Analcime
by Wei Xie, Hao Ma, Chuangguang Cao, Yating Wang, Yanhui Qiao, Junjiang Teng, Ning Li and Chaochao Yue
Materials 2025, 18(12), 2818; https://doi.org/10.3390/ma18122818 - 16 Jun 2025
Viewed by 336
Abstract
Analcime has demonstrated potential for a variety of applications in technology, especially in adsorption and heterogeneous catalysis. In this study, synthetic analcime was investigated by using sea sand as a silica source. Sea sand was first treated with HNO3 and NaOH. The [...] Read more.
Analcime has demonstrated potential for a variety of applications in technology, especially in adsorption and heterogeneous catalysis. In this study, synthetic analcime was investigated by using sea sand as a silica source. Sea sand was first treated with HNO3 and NaOH. The pretreated sea sand as the silica resource and Al(NO3)3 as the aluminum source were used for the hydrothermal synthesis of analcime with different ratios of Si/Al and Na/Si. The products obtained under different conditions were characterized by X-ray diffraction. The results showed that analcime synthesized using acid-treated sea sand was mixed with other impurities, such as quartz and sodalite. Pure analcime was obtained using alkali-treated sea sand as the silica source. The analcime prepared under an optimized synthesis condition was further investigated via SEM, FT-IR, and TG. The particle size of the prepared analcime ranged from 40 to 50 μm. The adsorption ability of analcime was studied, and the Cu2+ adsorption process was found to follow a pseudo-second-order kinetic model. Full article
(This article belongs to the Special Issue Application and Modification of Clay Minerals)
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31 pages, 16566 KiB  
Article
The Role of Fluid Chemistry in the Diagenetic Transformation of Detrital Clay Minerals: Experimental Insights from Modern Estuarine Sediments
by Anas Muhammad Salisu, Abdulwahab Muhammad Bello, Abduljamiu O. Amao and Khalid Al-Ramadan
Minerals 2025, 15(3), 317; https://doi.org/10.3390/min15030317 - 19 Mar 2025
Viewed by 697
Abstract
The diagenetic transformation of detrital clay minerals significantly influences sandstone reservoir quality, with fluid chemistry and temperature playing key roles in dictating transformation pathways during burial diagenesis. While these processes are well-documented in basinal settings, the diagenetic alterations of sediments in dynamic environments [...] Read more.
The diagenetic transformation of detrital clay minerals significantly influences sandstone reservoir quality, with fluid chemistry and temperature playing key roles in dictating transformation pathways during burial diagenesis. While these processes are well-documented in basinal settings, the diagenetic alterations of sediments in dynamic environments like estuaries remain underexplored. This study investigates the impact of fluid composition on the transformation of modern estuarine sediments through hydrothermal experiments using sediments from the Gironde estuary, SW France. A range of natural and synthetic solutions including seawater (SW), 0.1 M KCl (SF1), 0.1 M NaCl, KCl, CaCl2·2H2O, MgCl2·6H2O (SF2), estuarine water (EW), and 0.1 M Na2CO3 (SF3) were used under temperatures from 50 °C to 250 °C for 14 days, with a fixed fluid-to-sediment ratio of 10:1. The results revealed distinct mineralogical transformations driven by fluid composition. Dissolution of detrital feldspars and clay materials began at lower temperatures (<100 °C). The authigenic formation of smectite and its subsequent illitization in K-rich fluids (SW, SF1) occurred between 150 °C and 250 °C, replicating potassium-driven illitization processes observed in natural sandstones. Additionally, chlorite formation occurred through the conversion of smectite in SF2 and EW. Geochemical analysis showed that SF2 produced Mg-rich chlorites, while EW yielded Fe-rich chlorites. This aligns with diagenetic trends in coastal environments, where Fe-rich chlorites are typically associated with estuarine systems. The resulting authigenic illite and chlorite exhibited morphological and chemical characteristics similar to those found in natural sandstones, forming through dissolution-crystallization and solid-state transformation mechanisms. In contrast to illite and chlorite, SF3 produced entirely different mineral phases, including halite and analcime (zeolite), attributed to the high alkalinity and Na-rich composition of the solution. These findings provide valuable insights into the role of fluid chemistry in the diagenetic alteration of modern sediments and their implications for the evolution of sandstone reservoirs, which is critical for energy exploration and transition. Full article
(This article belongs to the Section Clays and Engineered Mineral Materials)
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18 pages, 5233 KiB  
Article
Alkaline Hydrothermal Treatment of Chabazite to Enhance Its Ammonium Removal and Recovery Capabilities through Recrystallization
by Dipshika Das and Sukalyan Sengupta
Processes 2024, 12(1), 85; https://doi.org/10.3390/pr12010085 - 29 Dec 2023
Cited by 4 | Viewed by 1586
Abstract
The treatment of chabazite (CHA), a natural zeolite, with the alkaline hydrothermal method to improve its ion-exchange capacity is a widely adopted route by environmental scientists for the purpose of better ammonium (NH4+) removal from wastewater. This work [...] Read more.
The treatment of chabazite (CHA), a natural zeolite, with the alkaline hydrothermal method to improve its ion-exchange capacity is a widely adopted route by environmental scientists for the purpose of better ammonium (NH4+) removal from wastewater. This work addresses a noteworthy trend in environmental science, where researchers, impressed by the increased ion-exchange capacity achieved through alkaline hydrothermal treatment, often bypass the thorough material characterization of treated CHA. The prevalent misconception attributes the improved features solely to the parent zeolitic framework, neglecting the fact that corrosive treatments like this can induce significant alterations in the framework and those must be identified with correct nomenclature. In this work, alkaline-mediated hydrothermally treated CHA has been characterized through X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), solid-state magic-angle spinning nuclear magnetic resonance (MAS-NMR), high-resolution transmission electron microscopy (HRTEM), and energy-dispersive X-ray spectroscopy (EDS) and it is concluded that the treated samples have been transformed into a desilicated, aluminum (Al)-dense framework of analcime (ANA) with a low silica–alumina ratio and with a strikingly different crystal shape than that of parent CHA. This treated sample is further examined for its NH4+ removal capacity from synthetic wastewater in a fixed-bed column arrangement. It achieved a maximum NH4+ removal efficiency of 4.19 meq/g (75.6 mg/g of NH4+), twice that of the parent CHA. Moreover, the regeneration of the exhausted column yielded a regenerant solution, with 94% reclaimed NH4+ in it, which could be used independently as a nitrogenous fertilizer. In this work, the meticulous compositional study of zeolitic materials, a well-established practice in the field of material science, is advocated for adoption by environmental chemists. By embracing this approach, environmental scientists can enhance their comprehension of the intricate changes induced by corrosive treatments, thereby contributing to a more nuanced understanding of zeolitic behavior in environmental contexts. Full article
(This article belongs to the Section Environmental and Green Processes)
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16 pages, 12193 KiB  
Article
Fusion-Assisted Hydrothermal Synthesis of Technogenic-Waste-Derived Zeolites and Nanocomposites: Synthesis, Characterization, and Mercury (II) Adsorption
by Madina Suleimenova, Saule Zharylkan, Meruyert Mekenova, Alibek Mutushev, Seytkhan Azat, Aidana Tolepova, Alzhan Baimenov, Aliya Satayeva and Zhandos Tauanov
Int. J. Mol. Sci. 2023, 24(14), 11317; https://doi.org/10.3390/ijms241411317 - 11 Jul 2023
Cited by 8 | Viewed by 1762
Abstract
This study presents the synthesis of zeolites derived from coal fly ash (CFA) using the fusion-assisted alkaline hydrothermal method. The zeolites were synthesized by combining CFA and NaOH at a molar ratio of 1:1.2 under fusion temperatures of 500, 600, and 700 °C. [...] Read more.
This study presents the synthesis of zeolites derived from coal fly ash (CFA) using the fusion-assisted alkaline hydrothermal method. The zeolites were synthesized by combining CFA and NaOH at a molar ratio of 1:1.2 under fusion temperatures of 500, 600, and 700 °C. Subsequently, the obtained zeolites were subjected to further modifications through the incorporation of magnetic (Fe3O4) and silver (Ag0) nanoparticles (NPs). The Fe3O4 NPs were introduced through co-precipitation of Fe(NO3)2 and FeCl3 at a molar ratio of 1:1, followed by thermal curing at 120 °C. On the other hand, the Ag0 NPs were incorporated via ion exchange of Na+ with Ag+ and subsequent reduction using NaBH4. The synthesized porous materials exhibited the formation of zeolites, specifically analcime and sodalite, as confirmed by X-ray diffraction (XRD) analysis. Additionally, the presence of Fe3O4 and Ag0 NPs was also confirmed by XRD analysis. The elemental composition analysis of the synthesized nanocomposites further validated the successful formation of Fe3O4 and Ag0 NPs. Nitrogen porosimetric analysis revealed the formation of a microporous structure, with the BET surface area of the zeolites and nanocomposites ranging from 48.6 to 128.7 m2/g and pore sizes ranging from 0.6 to 4.8 nm. The porosimetric characteristics of the zeolites exhibited noticeable changes after the modification process, which can be attributed to the impregnation of Fe3O4 and Ag0 NPs. The findings of this research demonstrate the effectiveness of the fusion-assisted method in producing synthetic zeolites and nanocomposites derived from CFA. The resulting composites were evaluated for their potential application in the removal of mercury ions from aqueous solutions. Among the samples tested, the composite containing Ag0 NPs exhibited the highest adsorption capacity, reaching 107.4 mg of Hg2+ per gram of composite. The composites modified with Fe3O4 NPs and Ag/Fe3O4 nanocomposites displayed adsorption capacities of 68.4 mg/g and 71.4 mg/g, respectively. Full article
(This article belongs to the Special Issue Nanocomposites, Hybrids and Nanocrystalline Materials)
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12 pages, 1063 KiB  
Article
Column Adsorption Studies for the Removal of Ammonium Using Na-Zeolite-Based Geopolymers
by Elavarasi Sundhararasu, Hanna Runtti, Teija Kangas, Janne Pesonen, Ulla Lassi and Sari Tuomikoski
Resources 2022, 11(12), 119; https://doi.org/10.3390/resources11120119 - 11 Dec 2022
Cited by 12 | Viewed by 4079
Abstract
The aim of this study was to examine the removal of ammonium ions from a synthetic model solution by using Na-zeolite-based geopolymers. Na-zeolite (=analcime) is a residue from mining industry. Three adsorbents were prepared from Na-zeolite using different production steps and metakaolin as [...] Read more.
The aim of this study was to examine the removal of ammonium ions from a synthetic model solution by using Na-zeolite-based geopolymers. Na-zeolite (=analcime) is a residue from mining industry. Three adsorbents were prepared from Na-zeolite using different production steps and metakaolin as a blending agent. These novel adsorbents were investigated in a fixed-bed column system where the effects of different flow rates with the initial ammonium concentration of 40 mg/L were studied. The Thomas, Bohart–Adams and Yoon–Nelson breakthrough curve models fitted well with the experimental data with a high R2 value. After adsorption experiments, adsorbents were regenerated using a mixture of 0.2 M NaCl and 0.1 M NaOH as a regeneration agent; after that, adsorbents were reutilised for ammonium ion adsorption for three adsorption–regeneration cycles. The results of the experiment indicate that all the prepared analcime-based geopolymers are suitable adsorbents for the removal of ammonium ions and that capacity remains nearly constant for two of them during two adsorption–regeneration cycles. Full article
(This article belongs to the Special Issue Women's Special Issue Series: Sustainable Resource Management)
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26 pages, 3358 KiB  
Article
Fe3+/Mn2+ (Oxy)Hydroxide Nanoparticles Loaded onto Muscovite/Zeolite Composites (Powder, Pellets and Monoliths): Phosphate Carriers from Urban Wastewater to Soil
by Diana Guaya, Luz Maza, Adriana Angamarca, Eda Mendoza, Luis García, César Valderrama and José Luis Cortina
Nanomaterials 2022, 12(21), 3848; https://doi.org/10.3390/nano12213848 - 31 Oct 2022
Cited by 5 | Viewed by 1952
Abstract
The development of an efficient adsorbent is required in tertiary wastewater treatment stages to reduce the phosphate–phosphorous content within regulatory levels (1 mg L−1 total phosphorous). In this study, a natural muscovite was used for the preparation of muscovite/zeolite composites and the [...] Read more.
The development of an efficient adsorbent is required in tertiary wastewater treatment stages to reduce the phosphate–phosphorous content within regulatory levels (1 mg L−1 total phosphorous). In this study, a natural muscovite was used for the preparation of muscovite/zeolite composites and the incorporation of Fe3+/Mn2+ (oxy)hydroxide nanoparticles for the recovery of phosphate from synthetic wastewater. The raw muscovite MC and the obtained muscovite/sodalite composite LMC were used in the powder form for the phosphate adsorption in batch mode. A muscovite/analcime composite was obtained in the pellets PLMCT3 and monolith SLMCT2 forms for the evaluation in fixed-bed mode for continuous operation. The effect of pH, equilibrium and kinetic parameters on phosphate adsorption and its further reuse in sorption–desorption cycles were determined. The characterization of the adsorbents determined the Fe3+ and Mn2+ incorporation into the muscovite/zeolite composite’s structure followed the occupancy of the extra-framework octahedral and in the framework tetrahedral sites, precipitation and inner sphere complexation. The adsorbents used in this study (MC, LMC, PLMCT3 and SLMCT2) were effective for the phosphate recovery without pH adjustment requirements for real treated wastewater. Physical (e.g., electrostatic attraction) and chemical (complexation reactions) adsorption occurred between the protonated Fe3+/Mn2+ (oxy)hydroxy groups and phosphate anions. Higher ratios of adsorption capacities were obtained by powder materials (MC and LMC) than the pellets and monoliths forms (PLMCT3 and SLMCT2). The equilibrium adsorption of phosphate was reached within 30 min for powder forms (MC and LMC) and 150 min for pellets and monoliths forms (PLMCT3 and SLMCT2); because the phosphate adsorption was governed by the diffusion through the internal pores. The adsorbents used in this study can be applied for phosphate recovery from wastewater treatment plants in batch or fixed-bed mode with limited reusability. However, they have the edge of environmentally friendly final disposal being promissory materials for soil amendment applications. Full article
(This article belongs to the Special Issue Advanced Nanocomposite Materials for Water and Wastewater Treatment)
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