Search Results (82)

Chabazite, a tectosilicate mineral, belongs to the zeolite group and has been widely used for the adsorptive removal of a number of cationic contaminants from the aqueous phase. However, a negatively charged chabazite surface can be altered by chemical modification in order to change its adsorption abilities towards anions. This study reports the potential for the removal of hexavalent chromium ions from aqueous solutions by modified chabazite. In this regard, natural chabazite was modified by the immobilization of HDTMA-Br to achieve double-layer coverage on its surface, defined as the double external cation exchange capacity. Next, a batch adsorption system was applied to study the adsorption of inorganic Cr(VI) anions from aqueous solutions. The process equilibrium was described by 11 theoretical isotherm equations, while 6 adsorption kinetics were represented by four models. Among those tested, the most appropriate model for the description of the studied process kinetics was the pseudo-second order irreversible model. The obtained results suggest that Cr(VI) adsorption takes place according to a complex mechanism comprising both Langmuir-type sorption with the maximum adsorption capacity of modified chabazite, approx. 9.3–9.9 mg g⁻¹, and the trapping of Cr(VI) inside the capillaries of the amorphous sorbent, making it a viable option for water treatment applications. Full article

Under China’s “dual carbon” goals (carbon peaking and carbon neutrality), the utilization of high-chlorine coal faces significant challenges due to its abundant reserves in regions such as Xinjiang and its notable environmental impacts. This study systematically investigates the combustion characteristics, environmental risks, and control strategies for high-chlorine coal. Key findings reveal that chlorine release occurs in three distinct stages, namely low-temperature desorption, medium-temperature organic bond cleavage, and high-temperature inorganic decomposition, with release kinetics governed by coal metamorphism and the reaction atmosphere. Chlorine synergistically enhances mercury oxidation through low-activation-energy pathways but exacerbates boiler corrosion via chloride–sulfate interactions. Advanced control technologies—such as water washing, calcium-based sorbents, and integrated pyrolysis–gasification systems—demonstrate substantial emission reductions. However, challenges remain in addressing high-temperature corrosion and optimizing multi-pollutant synergistic control. This study provides critical insights into the clean utilization of high-chlorine coal, supporting sustainable energy transitions. Full article

In this study, polymer films based on the inorganic sorbents Al₂O₃, ZrO₂ and SiO₂-phenyl with repellent N,N-diethyl-3-methylbenzamide were prepared and used as functional textile coatings. The high sorption activity of oxides with respect to N,N-diethyl-3-methylbenzamide (63–239 mg/g) allows for the use of these compounds as repellent carrier materials, and their mixture with polyacrylates allows for the formation of functional coatings–polymer films. Scanning electron microscopy and Fourier transform infrared spectroscopy results revealed that the inorganic sorbents Al₂O₃, ZrO₂ and SiO₂-phenyl were successfully anchored in the polyacrylate structure, and the FTIR spectra confirmed the presence of repellent molecules. The thermal diffusion parameters of N,N-diethyl-3-methylbenzamide were also calculated via thermogravimetric analysis and high-performance liquid chromatography with diode array detection. The highest thermal diffusion rates and concentrations were observed for the material with Al₂O₃ (up to 148.3∙10⁻⁹ mol at 200 °C), and lower values for ZrO₂ and SiO₂-phenyl (up to 15.2∙10⁻⁹ mol and 34.3∙10⁻⁹ mol at 200 °C, respectively). The heat flux parameter J_f was also calculated according to Onsager’s theory and Fourier’s law. The release of repellent from polymeric materials can be achieved by applying less heat than that required to reach the boiling point of N,N-diethyl-3-methylbenzamide. Full article

A sol-gel approach was used to prepare a thin hydrogel membrane based on an organic-inorganic polymer matrix embedded with pre-synthesized gold nanoparticles (AuNPs). The organic polymers utilized were poly(vinyl alcohol) (PVA) and poly(ethylene oxide) 400 (PEO) while tetraethoxysilane (TEOS) served as a precursor for the inorganic silica polymer. AuNPs were synthesized using D-glucose as a reducing agent and starch as a capping agent. A mixture of PVA, PEO, pre-hydrolyzed TEOS, and AuNP dispersions was cast and dried at 50 °C to obtain the hybrid hydrogel membrane. The structure, morphology, and optical properties of the nanocomposite membrane were analyzed using TEM, SEM, XRD, and UV-Vis spectroscopy. The newly designed hybrid hydrogel membrane was utilized as an efficient sorbent for the simultaneous speciation analysis of valence species of chromium and manganese in water samples via solid-phase extraction. This study revealed that Cr(III) and Mn(II) could be simultaneously adsorbed onto the PVA/PEO/SiO₂/AuNP membrane at pH 9 while Cr(VI) and Mn(VII) remained in solution due to their inability to bind under these conditions. Under optimized parameters, detection limits and relative standard deviations were determined for chromium and manganese species. The developed analytical method was successfully applied for the simultaneous speciation analysis of chromium and manganese in drinking water and wastewater samples. Full article

Although total selenium content is still useful in many areas, knowledge of its speciation is gaining importance as its various chemical forms have different environmental effects, toxicities and biological utilization. Among several methods used for the isolation and enrichment of selenium species, solid-phase extraction and its alternative approaches are often applied due to their simplicity and high efficiency. This brief overview summarizes the progress made in using different nanostructure sorbents to separate and preconcentrate inorganic selenium species in environmental waters. Nanomaterials are finding increasing applications as they have a large specific surface area and high chemical stability. Functionalizing their surface by covalent or noncovalent interactions with other components, grafting or doping with heteroatoms can improve the separation and removal efficiency. Strategies based on combining selective chemical reactions and separation procedures are discussed. Full article

Metal–organic frameworks (MOFs) are hybrid inorganic–organic 3D coordination polymers with metal sites and organic linkers, which are a “hot” topic in the research of sorption, separations, catalysis, sensing, and environmental remediation. In this study, we explore the molecular mechanism and kinetics of interaction of the new copper porphyrin aluminum metal–organic framework (actAl-MOF-TCPPCu) compound 4 with a vapor of the volatile organic sulfur compound (VOSC) diethyl sulfide (DES). First, compound 4 was synthesized by post-synthetic modification (PSM) of Al-MOF-TCPPH₂ compound 2 by inserting Cu²⁺ ions into the porphyrin ring and characterized by complementary qualitative and quantitative chemical, structural, and spectroscopic analysis. Second, the interaction of compound 4 with DES vapor was analyzed dynamically by the novel method of in situ time-dependent attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy at controlled humidity levels. The sorbent–adsorbate interactions, as analyzed by the shifts in IR peaks, indicate that the bonding includes the hydroxy O-H, carboxylate COO⁻, and phenyl groups. The kinetics of sorption obeys the Langmuir pseudo-first-order rate law. The pre-adsorption of water vapor by compound 4 at the controlled relative humidity under static (equilibrium) conditions yields the binary stoichiometric adsorption complex (Al-MOF-TCPPCu)_1.0(H₂O)_8.0. The pre-adsorption of water vapor makes the subsequent sorption of DES slower, while the kinetics obey the same rate law. Then, static pre-adsorption of water vapor was followed by static sorption of DES vapor, and the ternary adsorption complex (Al-MOF-TCPPCu)_1.0(H₂O)_8.0(DES)₃.₈ was obtained. Despite the pre-adsorption of significant amounts of water, the binary complex adsorbs a large amount of DES: ca. 36.6 wt. % (per compound 4). Finally, the ternary complex is facilely regenerated by gentle heating under vacuum. Compound 4 and related MOFs are promising for adsorptive removal of vapor of DES and related VOSCs from dry and humid air. Full article

With an output of more than two million tons of alumina per year, Venezuela is an important producer. As observed, this mining extraction activity generates a large number of by-products poorly valorized for many reasons (economic, technical, and due to environmental standards and regulations) Venezuela production generates wastes (more than 15 million of m³) called red muds, which are dumped in old lagoons near the Orinoco river or stored. This sludge has a high alkalinity (pH between 10 and 13) and a chemical composition containing some heavy metals (40 ppm Cr, 107 ppm La, 178 ppm Ce) that means it is considered environmentally problematic waste. However, their mineralogical, textural and structural characteristics make them adsorption materials. So, the aim of the study presented here was to investigate the sorption properties of these residues in the case of treatment of water from acid mine drainage. In fact, with an important reactive surface, their capacities to trap by adsorption trace elements such as cadmium, lead or zinc has been studied. Batch sorption tests revealed significant retention of contaminants such as Pb, Zn and As. These retention processes were interpreted using the Langmuir isotherm model. The promising first results indicate that the red mud named Venezuelan bauxite residue (VBR) reveals its great potential as a sorbent of inorganic pollutants. The sorption process is chemically dependent and efficient for certain pH and IS ranges. In addition, the material showed a strong affinity for the adsorption of arsenate (As⁵⁺). This was observed during post adsorption chemical speciation experiments, through the very high affinity of this element for the least mobile fractions, including oxyhydroxides mobile fractions, including Fe oxyhydroxides (amorphous). Nevertheless, these mining by-products could be considered as valuable absorbent materials. Despite this promising results, further studies are required to evaluate their potential in different conditions (dynamic tests, pH, IS, inorganic and organic contaminants, concentration and time effect). Full article

The escalating demand for lithium has intensified the need to process critical lithium ores into battery-grade materials efficiently. This review paper overviews the transformation processes and cost of converting critical lithium ores, primarily spodumene and brine, into high-purity battery-grade precursors. We systematically examine the study findings on various approaches for lithium recovery from spodumene and brine. Dense media separation (DMS) and froth flotation are the most often used processes for spodumene beneficiation. Magnetic separation (MS) and ore gravity concentration techniques in spodumene processing have also been considered. To produce battery-grade lithium salts, the beneficiated-concentrated spodumene must be treated further, with or without heat, in the presence of acidic or alkaline media. As a result, various pyro and hydrometallurgical techniques have been explored. Moreover, the process of extracting lithium from brine through precipitation, liquid–liquid extraction, and polymer inclusion membrane separation employing different organic, inorganic, and composite polymer sorbents has also been reviewed. Full article

This article provides an overview of the use of layered double hydroxides (LDHs) as effective sorbents in various extraction methods, including column-based solid-phase extraction (SPE), dispersive solid-phase extraction (DSPE), and magnetic solid-phase extraction (MSPE), for the separation and preconcentration of inorganic oxyanions of chromium, arsenic, and selenium. The primary focus is on enhancing the analytical performance of spectrometric detection techniques, particularly in terms of sensitivity and selectivity when analyzing low concentrations of target analytes in complex matrices. LDHs, which can be readily prepared and structurally modified with various substances, offer promising potential for the development of novel analytical methods. When used in analytical extraction procedures and following careful optimization of experimental conditions, the developed methods have yielded satisfactory results, as documented by studies reviewed in this paper. This review is intended to assist analytical chemists in scientific laboratories involved in developing new extraction procedures. Full article

For many decades, natural and modified clay minerals have been used as adsorbents to clean up aquatic and soil ecosystems contaminated with organic and inorganic pollutants. In this study, organoclays based on bentonite and various amphoteric and nonionic surfactants were synthesized and tested as effective sorbents for lead ions. The maximum values of R were obtained when describing the sorption processes using the Langmuir model, which ranged from 0.97 to 0.99. The adsorption of lead ions by these organoclays was investigated using different sorption models including the Langmuir, Freundlich, and BET. It was found that, according to the values of limiting adsorption to the Langmuir equation, the synthesized organoclays formed an increasing series: organoclay with cocamide diethanolamine < bentonite < organoclay with lauramine oxide < organoclay with sodium cocoiminodipropionate < organoclay with disodium cocoamphodiacetate < organoclay with alkyl polyglucoside. The Gibbs energy for all of the analyzed samples was calculated and found to be negative, indicating the spontaneity of the cation adsorption process in the forward direction. The maximum value of the adsorption capacity of lead cations on organoclay-based bentonite with alkyl polyglucoside was 1.49 ± 0.05 mmol/g according to the Langmuir model, and 0.523 ± 0.003 mmol/g as determined by the BET model. In the process of modifying bentonite, there was an increase in negative values of the zeta potential for organoclays compared to the initial mineral, which clearly enhanced their electrostatic interactions with the positively charged lead ions. It was hypothesized, based on the physicochemical principles, that exchange adsorption is the main mechanism for lead absorption. Based on chemical approaches, organoclays based on amphoteric surfactants absorb lead mainly through the mechanisms of electrostatic attraction, ion exchange, and complexation as well as the formation of insoluble precipitates. Organoclays based on nonionic surfactants, on the other hand, absorb lead through mechanisms of complexation (including chelation) and the formation of insoluble chemical precipitates. The comparison of isotherms from different models allows us to find the most accurate match between the model and the experimental data, and to better understand the nature of the processes involved. Full article

The presence of pharmaceuticals or their active metabolites in receiving waters is a sign of the inefficient removal of bioactive substrates from wastewater. Adsorption seems to be the most effective and inexpensive method of their removal. Waste management aimed at sorbents is a promising way to sustain several sustainable development goals. In the presented paper, the removal of the two most widely used drugs in the wastewater was examined. Diclofenac and carbamazepine were removed from water and wastewater using textile waste-derived sorbents. Their removal efficiency was verified by testing several process parameters such as the time of the sorption, the presence of interfering inorganic ions, the presence of dissolved organic matter, the initial pH and ionic strength of the solution, and various water matrices. The adsorption capacity was noted for diclofenac (57.1 mg/g) and carbamazepine (21.25 mg/g). The tested process parameters (pH, presence of inorganic ions, dissolved organic matter, ionic strength, water matrix) confirmed that the presented waste materials possessed a great potential for pharmaceutical removal from water matrices. Full article

Contaminated sediments may induce long-term risks to humans and ecosystems due to the accumulation of priority and emerging inorganic and organic pollutants having toxic and bio-accumulation properties that could become a secondary pollution source. This study focused on the screening of novel bio-based materials to be used in the decontamination of marine sediments considering technical and environmental criteria. It aimed to compare the environmental impacts of cellulose-based adsorbents produced at lab scale by using different syntheses protocols that involved cellulose functionalization by oxidation and branching, followed by structuring of an aerogel-like material via Soxhlet extraction and freeze-drying or their combination. As model pollutants, we used 4-nitrobenzaldehyde, 4-nitrophenol, methylene blue, and two heavy metals, i.e., cadmium and chromium. When comparing the three materials obtained by only employing the Soxhlet extractor with different solvents (without freeze-dying), it was observed that the material obtained with methanol did not have a good structure and was rigid and more compact than the others. A Life Cycle Assessment (LCA) was conducted to evaluate the environmental performance of the novel materials. Apart from the hierarchical categorization of the materials based on their technical and environmental performance in eliminating organic pollutants and heavy metal ions, it was demonstrated that the cellulose-based material obtained via Soxhlet extraction with ethanol was a better choice, since it had lower environmental impacts and highest adsorption capacity for the model pollutants. LCA is a useful tool to optimize the sustainability of sorbent materials alongside lab-scale experiments and confirms that the right direction to produce new performant and sustainable adsorbent materials involves not only choosing wastes as starting materials, but also optimizing the consumption of electricity used for the production processes. The main results also highlight the need for precise data in LCA studies based on lab-scale processes and the potential for small-scale optimization to reduce the environmental impacts. Full article

The rapid industrial development of civilization has led to the need for the development of new materials to clean up chemically contaminated wastewater and soils. Organoclays, based on smectite minerals and various types of surfactants, are one of the most effective sorbents for adsorbing organic and inorganic pollutants. Organoclays are clay minerals that have been modified by the intercalation or grafting of organic molecules. The main mechanism of interaction between organic substances and organoclays involves the adsorption of the substances onto the surface of the clay mineral, which has an expanded structural cell. Various types of surfactants can be used to synthesize organoclays, including cationic, anionic, and amphoteric surfactants. Each type of surfactant has different properties that affect the clay’s ability to sorb. Cationic forms of trace elements, such as heavy metals, can also be adsorbed by organoclays. Data on the adsorption of these substances by organoclays are provided, along with information on how to synthesize them using various surfactants. This review also discusses the main mechanisms of interaction between these substances and clays and the various methods used to create organoclays. It is clear that the adsorption of heavy metals by organoclays is not influenced by their structure or properties, as they belong to the category of surfactant, but rather by their overall chemical structure and characteristics. The wide variety of surfactant types leads to different effects on the adsorption properties of trace elements. Full article

A new ionic liquid modified polymer gel containing methylimidazolium groups (poly(MIA)) is proposed as a sorbent for the separation and enrichment of trace inorganic and organic arsenic species in surface waters. The poly(MIA) was synthesized by chemical modification of polymeric precursor using post-polymerization modification of poly(glycidyl methacrylate-co-trimethylolpropane trimethacrylate). The composition, structure, morphology, and surface properties of the prepared particles were characterized using elemental analysis, Fourier transform infrared spectroscopy, scanning electron microscopy, and nitrogen adsorption–desorption measurements. Optimization experiments showed that at pH 8, monomethylarsonic acid (MMAs), dimethylarsinic acid (DMAs), and As(V) were completely retained on the poly(MIA), while the sorption of As(III) was insignificant. The desorption experiments revealed that due to the weaker binding of organic arsenic species, selective elution with 1 mol/L acetic acid for MMAs + DMAs, followed by elution with 2 mol/L hydrochloric acid for As(V), ensured their quantitative separation. The adsorption kinetic and mechanism were defined. The analytical procedure for As(III), As(V), MMAs, and DMAs determination in surface waters was developed and validated through the analysis of certified reference material. Full article

Pharmaceuticals and heavy metals pose significant risks to human health and aquatic ecosystems, necessitating their removal from water and wastewater. A promising alternative for this purpose involves their removal by adsorption on composite sorbents prepared using a conventional layer-by-layer (LbL) method or an innovative coacervate direct deposition approach. In this study, four novel composite materials based on a silica core (IS) and a polyelectrolyte coacervate shell were used for the investigation of dynamic adsorption of three heavy metals (lead, nickel and cadmium) and an organic drug model (diclofenac sodium salt, DCF-Na). The four types of composite sorbents were tested for the first time in dynamic conditions (columns with continuous flow), and the column conditions were similar to those used in wastewater treatment plants. The influence of the polyanion nature (poly(acrylic acid) (PAA) vs. poly(sodium methacrylate) (PMAA)), maintaining a constant poly(ethyleneimine) (PEI), and the cross-linking degree (r = 0.1 and r = 1.0) of PEI chains on the immobilization of these pollutants (inorganic vs. organic) on the same type of composite was also studied. The experiments involved both single- and multi-component aqueous solutions. The kinetics of the dynamic adsorption process were examined using two non-linear models: the Thomas and Yoon–Nelson models. The tested sorbents demonstrated good adsorption capacities with affinities for the metal ions in the following order: Pb²⁺ > Cd²⁺ > Ni²⁺. An increase in the initial diclofenac sodium concentration led to an enhanced adsorption capacity of the IS/(PEI-PAA)_c-r1 sorbent. The calculated sorption capacities were in good agreement with the adsorption capacity predicted by the Thomas and Yoon–Nelson models. The substantial affinity observed between DCF-Na and a column containing composite microparticles saturated with heavy metal ions was explained. Full article