Search Results (77)

Hexavalent chromium (Cr(VI)) is a highly toxic, non-biodegradable, and carcinogenic heavy metal. Its continuous release into aquatic ecosystems demands efficient, low-cost adsorbents. In this study, orange peel and peanut shell residues were thermally modified at 250 °C to enhance Cr(VI) remediation. Structural characterization confirmed that low-temperature calcination transforms raw agroindustrial wastes into functional biochars with a chemical architecture primed for cooperative Cr(VI) removal. N₂ physisorption revealed a hierarchical mesoporous network with average pore diameters of 30.6 nm (calcined orange peel) and 15.4 nm (calcined peanut shell), despite low specific surface areas. Batch adsorption experiments demonstrated that removal kinetics reached equilibrium within 5 min for the modified biochars. Isotherm modeling showed that the adsorption process was best described by the Freundlich and Sips models. The calculated Sips heterogeneity factors (β_S > 1) provided evidence of a cooperative multi-layer adsorption mechanism, attributed to the induced mesoporosity: initial chemisorption at high-energy sites facilitates the continuous anchoring of additional Cr(VI) ions without premature saturation. Ultimately, this study demonstrates that low-temperature calcination is a viable strategy to transform agricultural waste into kinetically efficient, cooperative adsorbents for wastewater treatment. Full article

Hexavalent chromium (Cr (VI)) contamination of water resources constitutes a major environmental and public health issue due to its high toxicity, mobility, and carcinogenic properties. This review examines recent advances in Cr (VI) removal technologies from water and wastewater, with emphasis on membrane-based separation processes and adsorption approaches. Conventional treatment methods, including chemical precipitation, ion exchange (IX), electrocoagulation (EC), electrodeionization (EDΙ), bioremediation, and photocatalysis, are comparatively discussed in terms of removal efficiency, operational limitations, and applicability. In parallel, sustainable adsorbent materials derived from biomass and agricultural waste are evaluated as environmentally friendly and cost-effective alternatives for chromium removal. The role of functional groups, adsorption mechanisms, and redox interactions involved in Cr (VI) reduction and immobilization is also analyzed. Attention is given to membrane technologies, such as reverse osmosis (RO), nanofiltration (NF), electrodialysis (ED), and ultrafiltration (UF) after surface modification with the incorporation of nanomaterials and/or the application of Layer-by-Layer (LBL) assembly techniques, which enhance selectivity, permeability, and antifouling behavior. The reviewed studies demonstrate that advanced membrane systems and bio-based adsorbents can achieve high chromium removal efficiencies while supporting sustainable water treatment practices. Overall, the combination of membrane technologies with functionalized materials represents a promising direction for the development of efficient and environmentally sustainable Cr (VI) remediation systems capable of meeting increasingly strict regulatory limits. Full article

For the removal of hexavalent chromium [Cr(VI)] from drinking water, a hybrid biosorbent designated chitosan–natural diatomaceous earth (CNDE) was developed and thoroughly characterized. The material couples the ion-exchange and chelating capacity of chitosan—applied at an 85% degree of deacetylation—with the high-surface-area mineral framework of natural diatomaceous earth, onto which the polymer was deposited as a conformal coating. Surface morphology and internal microstructure were examined by scanning and transmission electron microscopy (SEM/TEM), while elemental composition across the hybrid matrix was resolved by energy-dispersive X-ray spectroscopy (EDX). Fourier transform infrared (FTIR) spectroscopy was employed to identify the surface functional groups responsible for chromate binding, and streaming current measurements established the pH of zero charge (pH_pzc), which governs the electrostatic environment at the sorbent–solution interface. Specific surface area was quantified by the Brunauer–Emmett–Teller (BET) method, and the balance of surface acidic and basic sites was determined through titrimetric analysis of total acidity and alkalinity. Thermogravimetric analysis (TGA) was conducted to assess thermal stability. Batch equilibrium isotherm experiments were performed to evaluate Cr(VI) uptake from model drinking water prepared using dilute potassium dichromate solutions adjusted to target pH levels. The effects of solution pH and competing anions (chloride and sulfate) were also investigated. Kinetic studies were conducted to determine the rate of Cr(VI) adsorption, and residual metal concentrations were measured using inductively coupled plasma mass spectrometry (ICP-MS). Results indicated that CNDE containing 30% chitosan (CNDE30) achieved effective Cr(VI) removal at pH 5. Adsorption was strongly pH-dependent, decreasing as pH increased from 5 to 8. Equilibrium data were well described by both Langmuir and Freundlich isotherm models, while kinetic data followed a pseudo-second-order model. The presence of chloride ions (15 mg/L) reduced adsorption capacity by approximately one-third, whereas sulfate at the same concentration significantly inhibited Cr(VI) removal. Overall, the isotherm results suggest that CNDE30 is a promising material for Cr(VI) removal from drinking water. Its cost-effectiveness, ease of synthesis, and potential for reuse make it particularly attractive for small-scale and decentralized water treatment applications. Full article

Coagulation-based technologies are increasingly recognized as key for controlling fluoride and hexavalent chromium in urban water and wastewater. Combined geogenic and industrial sources often drive chronic exposure and create an underrecognized public health burden. This review synthesizes current knowledge on the occurrence, speciation, and toxicology of F⁻ and Cr(VI) in urban systems, links regulatory targets to health outcomes, and critically examines conventional, advanced, and electrochemical coagulation processes for their removal under realistic water-quality conditions. Mechanistic sections describe how aluminum-, iron-, magnesium- and zirconium-based coagulants, including pre-polymerized and composite formulations (e.g., IPC-type coagulants, PSiFAC-Mg, ZrCl₄), remove fluoride via Al–F complexation, Al–F–OH co-precipitation, ion exchange, and sweep flocculation, while Cr(VI) control relies on Fe(II)-mediated reduction to Cr(III), followed by adsorption and co-precipitation with metal hydroxides. The review assesses how water chemistry and operating conditions affect single- and multi-contaminant removal, highlighting competition among fluoride, Cr(VI), nutrients, and other oxyanions. Performance data from bench-, pilot-, and selected full-scale studies show that optimized coagulation and electrocoagulation can substantially reduce fluoride and Cr(VI) (to drinking-water-relevant levels) in diverse urban waters, but also reveal persistent issues of sludge generation and stability, residual metals, process robustness, and cost. The review identifies priorities, including long-term urban-scale assessments, low-toxicity green coagulants, life-cycle and health impact assessments, and real-time coagulation control for fluoride and Cr(VI). Full article

Major vibrational spectroscopy studies have focused on the preparation of chromium coatings via chemical processes (conversion coatings), and few studies have focused on electrochemical processes (electrodeposition). Initially, the chemical precursors were hexavalent chromium salts, but these compounds are now replaced by less toxic trivalent ions. There is a profound understanding of the process when vibrational spectroscopy is used in combination with other techniques. This is the case for chromium(VI) conversion coatings, and the results of several techniques, such as synchrotron infrared microspectroscopy, have made it possible to understand the structure of the two-layer coating and the chemical composition of each layer. Vibrational spectroscopy confirmed the mechanism for coating formation, in which ferricyanide was a redox mediator. In addition, vibrational spectroscopy was effective in determining the mechanism of corrosion resistance of the coatings. Conversely, there are very few studies on the electrodeposition of trivalent chromium ions, and the mechanics of electrodeposition are unknown. To simplify the use of spectroscopy, spectra of potassium dichromate and chromium(III) sulfate are presented as references for coating studies, and a compilation of $\mathrm{C}\mathrm{r}\left(\mathrm{I}\mathrm{I}\mathrm{I}\right)-\mathrm{O}$ and $\mathrm{C}\mathrm{r}\left(\mathrm{V}\mathrm{I}\right)-\mathrm{O}$ vibrational modes is provided to facilitate band assignment. Our review highlights that spectroscopic techniques have been insufficiently applied in this field; however, the results of vibrational spectroscopy accelerate the transition to safer Cr(III) technology. Full article

In this study, both trivalent and hexavalent forms of chromium were examined in urban and agricultural Mediterranean soils. Chromium partitioning in different soil fractions was studied. Pot experiments included contamination of soil samples using Cr solutions, as well as a further study regarding Cr distribution in naturally contaminated soils. The soils were subjected to quantitative determination of both the available and total Cr concentration, as well as Cu and Zn, which were naturally present in the soil samples. Metal concentrations in the soil fractions were quantified after the application of the BCR fractional extraction method. The numbers of both trivalent and hexavalent Cr ions in each extract were determined. Considerable discrepancies were noticed regarding the Cr content of each soil fraction in both municipal and cultivated soils, indicating the possible origin of the pollution. The increasing impact of pollution is a significant parameter for the availability of chromium ions in both agricultural and urban soils. Increased pollution durations resulted in a significant increase in the non-available fraction of toxic Cr (VI), mainly in urban soil. Variations were also observed in the chromium species, as changes in soil parameters and in the conditions of the experiment seem to affect the conversion of the less harmful trivalent chromium to the toxic hexavalent chromium. In urban soils, the amount of toxic Cr (VI) bound to iron and manganese oxides exceeds 37.8%, while in agricultural soils, the amount of Cr (VI) associated with soil organic matter reaches 35%. Knowing the mechanisms and variables influencing Cr availability in agricultural and urban Mediterranean soils is desirable, as safe living in ecologically acceptable fields and producing safe goods in healthy soil systems are paramount goals. Full article

We investigated the application of an adsorbent fabricated from satsuma mandarin peel biomass using coating with poly(glycidyl methacrylate) followed by sequential treatment with hydroxylamine and hydrochloric acid for the remediation of hexavalent chromium-polluted water. The adsorbent was characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Batch adsorption experiments were conducted wherein initial solution pH, initial chromium concentration, contact time, and temperature were varied. The adsorption equilibrium experimental data were well simulated by the Langmuir and Jovanovic models, pointing toward the formation of a monolayer of adsorbed chromium ions. The total chromium adsorption capacity of the functionalized satsuma mandarin peel adsorbent reached 219.28 mg g⁻¹ at initial pH 1.4 and 60 °C, markedly higher than 110.23 mg g⁻¹ at 30 °C. Where Cr(VI) was the sole chromium oxidation state in the initial solutions synthesized from potassium dichromate, the presence of Cr(III) ions in the final solutions confirmed Cr(VI) reduction. The results of this study show that the functionalized satsuma mandarin peel biomass is a potential candidate for use in the removal of hexavalent chromium from aqueous solution through reduction-coupled adsorption. Full article

Porous carbon-loaded MnO was prepared via a combination of the sol–gel method and the chemical blow molding method using polyvinylpyrrolidone (PVP) and manganese nitrate as starting materials. SEM, EDX, TEM, FTIR, XRD, XPS, nitrogen adsorption–desorption, and elemental analysis were used to assess its physical and chemical characteristics. Furthermore, the adsorption property of porous carbon-loaded MnO for hexavalent chromium (Cr(VI)) in polluted water was investigated in detail. The results demonstrated that large numbers of MnO nanoparticles were evenly mounted on the surfaces of carbon walls, with a uniform distribution of C, N, and O elements. The BET surface area was 46.728 m²/g, and the pore sizes of porous carbon ranged from 2 nm to 10 nm. Additionally, abundant surface functional groups were found in porous carbon-loaded MnO, a result consistent with XPS data and applicable to the adsorption of heavy metals from aqueous solutions containing Cr(VI). The Freundlich model fitted the adsorption isotherm well, and the pseudo−second−order model precisely matched the adsorption kinetics. According to the study results, the adsorption was multilayer, and the adsorption process involved an endothermic reaction. These results indicate that this is a feasible way to synthesize a high−efficiency adsorbent for the removal of harmful heavy−metal ions from wastewater. Full article

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

Hexavalent chromium (Cr(VI)) is of significant interest in the environmental field due to its high toxicity. Biochar is commonly used as an adsorbent for Cr(VI) removal from wastewater. However, its lower removal efficiency remains a persistent challenge. This study develops an iron-modified rice straw biochar through a simple precipitation and pyrolysis method and applies it for Cr(VI) removal in wastewater, which could convert waste into treasure and improve the adsorption performance of adsorbent. In the adsorption experiments, the results revealed that the adsorption efficiency of Cr(VI) reached 95.54% within 480 min (conditions: adsorbent dosage 2.67 g/L, pH 2.5, temperature 25 ± 2 °C). The Langmuir isotherm model was more suitable to describe the adsorption behavior of Cr(VI) by Fe-BC, and the fitted adsorption capacity achieved 10.03 mg/g. The experimental process was better described by the pseudo-second-order kinetic model, indicating that the adsorption process chemical adsorption was the rate-limiting step. The thermodynamic experiments revealed that the adsorption process of Cr(VI) by Fe-BC was spontaneous and endothermic. Column experiments demonstrated that a lower flow speed was beneficial to adsorption performance. Mechanistic studies highlighted the synergistic roles of electrostatic attraction, ion exchange, and reduction in Cr(VI) removal. These findings provide novel perspectives and innovative approaches for the development and application of adsorbents. Full article

Hexavalent chromium Cr (VI) compounds present in ilmenite concentrate not only pose significant environmental hazards due to their toxicity but also complicate further processing, interfering with technological operations in industrial production. The high chromium content in ilmenite concentrates hinders their conversion into titanium-containing slag, necessitating the removal of chromium ions to permissible residual levels to produce titanium dioxide. In this study, various sorbents were investigated for the removal of chromate ions from the industrial effluents generated during ilmenite concentrate processing. The sorbents examined included natural and modified diatomite, activated carbon, taurite (shungite), and the ion-exchange resin Lewatit M500. The structures of both natural and modified diatomite were analyzed using scanning electron microscopy (SEM). It was determined that natural diatomite samples consist of diatom frustules of various shapes and their fragments, with structural element sizes ranging from submicron dimensions to 50 µm. A mathematical analysis of the sorption data for hexavalent chromium ion removal from solutions was performed. The results demonstrated high sorption efficiencies for Lewatit M500 (98.34%) and diatomite modified with iron compounds (98.95%). The findings suggest that diatomite is a promising sorbent for chromate ion removal from wastewater due to its availability and potential for chemical modification. Full article

Hexavalent chromium (Cr(VI)) is toxic, carcinogenic, and harmful to biological systems. Common detection methods, such as colorimetry, atomic absorption spectrometry, ion chromatography, and biological systems, can only be used in the laboratory and do not provide real-time feedback. To address these limitations, the current study cloned the ChrB gene, which exhibits high specificity in detecting Cr(VI), and the ChrA gene, which exhibits high Cr(VI) tolerance, into Escherichia coli. This recombinant strain, ChrA–ChrB–E. coli, was integrated into a single-chamber microbial fuel cell for accurate continual monitoring over a wide range of Cr(VI) concentrations. ChrA–ChrB–E. coli thrived in temperatures from 25 °C to 45 °C and pH levels between 5 and 8. Its ability to reduce Cr(VI) remained consistent across Cr(VI) forms, carbon sources, and oxyanions. Cyclic voltammetry was employed to verify the electrical activity of the biosensor. The biosensor exhibited a detection limit of 0.0075 mg/L. Under conditions simulating the regulatory emission limit for Cr(VI) of 0.5 mg/L in industrial wastewater, the biosensor achieved a response time of 20 s during continual operation. When tested with synthetic wastewater containing Cr(VI) concentrations from 0.02 to 150 mg/L, the system exhibited high adaptability and facilitated stable monitoring (relative standard deviation ≤ 2.7%). Additionally, the biosensor’s accuracy (−1.73% to 2.5%) matched that of traditional batch methods, highlighting its suitability for real-time Cr(VI) monitoring in aquatic environments. Full article

Chromium salt fillers commonly used in current anti-corrosion coatings are highly toxic. However, due to the unique high–low valence transformation and passivation mechanisms of chromium-based functional fillers and their wide applicability, chromium-free coatings find it challenging to achieve the same performance and industry acceptance. This study introduces an innovative approach that uses zinc to reduce molybdate (MoO₄²⁻) in an acidic solution, thereby forming a multivalent MoO₄²⁻ system (PMZ system), and applies it to chromium-free insulating coating for oriented silicon steel. The effects of reductant dosage on the valence composition of molybdenum in the PMZ system and the corrosion resistance of the coating were investigated. Additionally, the difference in the valence composition of molybdenum between the PMZ system and the multivalent phosphomolybdate system (PMNZ system) and its impact on corrosion resistance were studied. The results indicate that the PMZ system contains trivalent molybdenum and hexavalent molybdenum, while the PMNZ system contains pentavalent molybdenum and hexavalent molybdenum. The systems leverage the reactivity of lower-valence molybdenum to delay the corrosion by reacting with oxygen while maintaining the original mechanism of molybdenum salt fillers and forming sediment with iron ions to form a passivation layer. As the content of trivalent molybdenum in the PMZ system increases, the corrosion resistance of the insulating coating improves. When the amount of zinc added in the PMZ system is 0.006 g, the relative proportion of trivalent molybdenum reaches 20.52%, and the salt spray resistance of the coating developed with the PMZ system reaches 248 h with a corrosion area of less than 5%. When the contents of the main components and sodium molybdate in the PMZ coating and the PMNZ coating are the same, the corrosion resistance of the PMZ coating, which contains trivalent molybdenum, is better than that of the PMNZ coating, and the salt spray resistance exceeds 192 h. Full article

Currently, water is being polluted via various anthropogenic activities, resulting in wastewater contaminated with multiple pollutants, including heavy metals. Hexavalent chromium is a toxic heavy metal that poses significant health risks upon exposure. Biocomposites are materials that are partially composed of organic substances that enhance different properties of a composite. The aim of this study was to evaluate the kinetic, isothermal, and thermodynamic behaviour of a cellulose-based biocomposite with polylactic acid (PLA) for the removal of Cr (VI) from synthetic water. The results indicated that the Freundlich and Elovich models provided the best fit for the isothermal and kinetic data, with R² values of 0.671 and 0.973, respectively, suggesting that the adsorption process was chemical in nature and occurred on a heterogeneous, multilayer surface. Additionally, the thermodynamic analysis revealed that the adsorption process was exothermic, irreversible, and non-spontaneous. This study presents an innovative approach to the removal of metal ions using a cellulose–PLA biocomposite for wastewater treatment, offering kinetic, isothermal, and thermodynamic data applicable to the adsorption of other heavy metals. Full article

NiFe-layered double hydroxide (NiFe-LDH) and La-, Mo- or W-doped NiFe-LDH microparticles (NiFeX-LDH, X = La, Mo, W) were synthesized via the co-precipitation method. Their adsorption characteristics were evaluated by the removal of methyl orange (MO) and hexavalent chromium (Cr⁶⁺). The effects of the metal ion doping type, doping concentration (0–3at%), pH and temperature on the MO adsorption properties were systematically studied. The results show that W-doped NiFe-LDH exhibits superior MO removal capacity compared to undoped or La- or Mo-doped NiFe-LDH at the same 1at% doping level, which is attributed to the increased layer charge density and strong affinity for the π-electron systems of MO molecules. The NiFeW-LDH-1at% sample demonstrated the best MO adsorption performance within the W-doping range of 0–3at%, achieving a superior adsorption capability of 666.67 mg/g with a significantly shorter equilibrium time (10–120 min) compared to the similar LDH. NiFeW-LDH-1at% showed promising reusability, with its adsorption efficiency remaining 78.3% of its initial level after five adsorption–desorption cycles. The MO uptake onto NiFeX-LDH was attributed to the combined effect of anion exchange and the attraction of layer charge. In addition, the adsorption of NiFeW-LDH-1at% matched well with the Langmuir isotherm model and pseudo-second-order kinetic model, indicating a monolayer and chemical adsorption. Furthermore, NiFeW-LDH-1at% effectively adsorbed of Cr₂O₇²⁻ in the aqueous solution, revealing that W doping significantly enhances Cr(VI) removal performance. The maximum theoretical adsorption capacity onto NiFeW-LDH-1at% reached 63.25 mg/g, which was notably higher than that of the pristine NiFe-LDH adsorbent (53.56 mg/g). Overall, the W-doped NiFe-LDH material, as a low-cost and highly efficient adsorbent, shows great potential for wastewater treatment application. Full article