Chromium Ions Research Articles

Efficient Cr(VI) remediation by electrospun composite porous nanofibers incorporating biomass with metal oxides and metal-organic framework

To develop a highly efficient adsorbent to remediate and remove hexavalent chromium ions (Cr(VI)) from polluted water, cellulose acetate (CA) and chitosan (CS), along with metal oxides (titanium dioxide (TiO2) and ferroferric oxide (Fe3O4)), and a zirconium-based metal-organic framework (UiO-66) were used to fabricate the composite porous nanofiber membranes through electrospinning. The adsorption performance, influencing factors, adsorption kinetics and isotherms of composite nanofiber membranes were comprehensively investigated. The multi-layer membrane with interpenetrating nanofibers and surface functional groups enhanced the natural physical adsorption and provided potential chemical sites. The thermal stability was improved by introducing TiO2 and UiO-66. CA/CS/UiO-66 exhibited the highest adsorption capacity (118.81 mg g−1) and removal rate (60.76%), which were twice higher than those of the control. The correlation coefficients (R2) of all the composite nanofibers regressed by the Langmuir model were significantly higher than those by the Freundlich model. The pseudo-first-order kinetic curve of CA/CS composite nanofibers showed the highest R2 (0.973), demonstrating that the whole adsorption process involved a combination of strong physical adsorption and weak chemical adsorption by the amino groups of CS. However, the R2 values of the pseudo-second-order kinetic model increased after incorporating TiO2, Fe3O4, and UiO-66 into the CA/CS composite nanofiber membranes since an enhanced chemical reaction with Cr (VI) occured during the adsorption

Polypyrrole Coating via Lemieux-von Rudloff Oxidation on Magnetite Nanoparticles for Highly Efficient Removal of Chromium(VI) from Wastewater.

An alternative way for the coating of polypyrrole (PPy) polymer on hydrophobic magnetite (Fe3O4) nanoparticles is reported here to capture toxic chromium ions, Cr (VI), present in water. Iron oxide magnetic nanoparticles (Fe3O4) were synthesized by the conventional coprecipitation technique using FeCl3·6H2O and FeSO4·7H2O iron precursors and subsequently modified with oleic acid (OA). Then OA-Fe3O4 hydrophobic nanoparticles were oxidized using the Lemieux-von Rudloff reaction to transfer OA into hydrophilic azelaic acid (AA) (HOOC(CH2)7COOH-modified magnetic nanoparticles (AA-Fe3O4). Finally, a PPy polymer coating was formed by a seeded polymerization of pyrrole, using AA-Fe3O4 as seeds. The average size of PPy/Fe3O4 nanocomposites is 12.33 nm and is almost spherical in shape. The surface composition is confirmed by FTIR and thermogravimetry analyses. An X-ray diffraction study confirmed the formation of highly crystalline Fe3O4 nanoparticles, and the crystallinity was retained after the surface modification. The adsorption study suggested that the Cr(VI) ion adsorption is highly pH-dependent and the maximum amount of adsorption is obtained at pH 2.0. The adsorption results revealed that the Langmuir model provided the best fit for the isotherm, with a maximum adsorption capacity reaching approximately 173.22 mg g-1 at 323 K. Spontaneous and endothermic adsorption processes were confirmed by evaluating the thermodynamic parameters obtained in this investigation. The kinetics study showed that the interaction between Cr(VI) ions and magnetic nanocomposites was directed by a pseudo-second-order rate process indicating chemisorption. The prepared PPy/Fe3O4 nanocomposites would be promising adsorbents to purify water by eliminating Cr(VI) metal ions from wastewater.

A promising approach for the removal of hexavalent and trivalent chromium from aqueous solution using low-cost biomaterial.

Heavy metal pollution is an enduring environmental challenge that calls for sustainable and eco-friendly solutions. One promising approach is to harness discarded plant biomass as a highly efficient environmental friendly adsorbents. In this context, a noteworthy study has spotlighted the employment of Euryale ferox Salisbury seed coat (E.feroxSC) for the exclusion of trivalent and hexavalent chromium ions. This study aims to transform discarded plant residue into a novel, environmentally friendly, and cost-effective alternative adsorbent, offering a compelling alternative to more expensive adsorption methods. By repurposing natural materials, we can contribute to mitigating heavy-metal pollution while promoting sustainable and economically viable solutions in environmental remediation. The effect of different parameters, i.e., chromium ions' initial concentration (5-25mg L-1), solution pH (2-7), adsorbent dosage (0.2-2.4g L-1), contact time (20-240min), and temperature (298-313K), were investigated. E.feroxSC proved highly effective, achieving 96.5% removal of Cr(III) ions at pH 6 and 97.7% removal of Cr(VI) ions at pH 2, with a maximum biosorption capacity of 18.33mg/g for Cr(III) and 13.64mg/g for Cr(VI), making it a promising, eco-friendly adsorbent for tackling heavy-metal pollution. The adsorption process followed the pseudo-second-order kinetic model, aligning well with the Langmuir isotherm, exhibited favorable thermodynamics, and was characterized as feasible, spontaneous, and endothermic with physisorption mechanisms. The investigation revealed that E.feroxSC effectively adsorbed Cr(VI) which could be rejuvenated in a basic solution with minimal depletion in its adsorption capacity. Conversely, E.feroxSC's adsorption of Cr(III) demanded rejuvenation in an acidic milieu, exhibiting comparatively less efficient restoration.

Advances in Water Resource Management: An In Situ Sensor Solution for Monitoring High Concentrations of Chromium in the Electroplating Industry

Concerning environmental safety and mitigating the risk of water pollution, the electroplating industry, historically reliant on the use of elevated concentrations of heavy metals to achieve high-quality products, faces a crucial challenge in monitoring wastewater enriched with these metals, notorious for their adverse effects on ecosystems and human health. Chromium, in both oxidation states Cr (III) and Cr (VI), emerges as a prominently employed metal, yielding noteworthy outcomes throughout the galvanisation process. This research showcases the prototype of an automatic in situ sensor tailored to industry sustainability efforts to facilitate real-time monitoring and efficient water management. This custom sensor, characterized by sensitivity, reliability, and user-friendliness, utilizes UV-Vis colorimetric principle to detect Cr in both oxidation forms ranging from grams per litre (g/L) to parts per million (ppm). This is made possible by the unique vibrant colours induced by chromium ions, enabling the precise measurement of analyte concentrations. Thanks to 3D printing, this sensor system interacts with customized parts, designed and validated through simulation processes, for filtering out particulate that may interfere with the analysis. The outcome represents a synergistic blend of technology and environmental responsibility, aligning industrial processes with the goal of safeguarding water resources and ecosystems.

Synthesis, characterization, and breakthrough modeling of low-cost graphene oxide-sand supported adsorbent filter for the separation of lead and chromium ions

The existence of lead and chromium ions in waterbodies severely affects the biological activities of aquatic creatures that directly affect human health. A graphene oxide-sand (GO-sand)-based composite filter has been successfully used as a Rapid Sand Filter (RSF) to remove Lead (II) and Chromium (III) ions in water. Boehm titration, FTIR, RAMAN, XRD, and SEM-EDX analyses confirmed GO-sand’s active sites, semicrystalline, and irregular morphology. Moreover, lead and chromium adsorption using a GO-sand composite was established by XPS and SEM-EDX analyses. The results of the batch study showed significant adsorption (289.68 mg g−1 and 258.87 mg g−1) along with significant removal (96.4 % and 95.6 %) of Pb (II) and Cr (III), respectively. Among Langmuir, Freundlich, and Liu isotherms, the adsorption isotherm showed an excellent fit with Liu isotherm. The response surface methodology (RSM) study suggested adequate quadratic models and exceptional covenant between the predicted and actual figures with a significant coefficient determination (R2 > 0.920). The kinetic study finding revealed the best fit for the Elovich kinetic model (R2 = 0.995 (Pb), R2 = 0.967 (Cr)), and the thermodynamics study confirmed endothermic adsorption. Pareto analysis confirmed that solution pH was the most significant parameter towards adsorption. Furthermore, the regenerated adsorbent demonstrated practical reusability up to four adsorption–desorption cycles, revealing the process’s sustainability.

Rapid wet grinding carbonation of sintering red mud for highly efficient CO2 sequestration and Cr solidification

Sintering red mud (SRM) is an alkaline and aqueous solid waste from bauxite sintering for alumina production. The challenges in the effective utilization of SRM are strong alkalinity, aqueous state and leaching toxicity of the heavy metals. Herein, a rapid wet grinding carbonation technique of simultaneous injection of CO2 in wet grinding process was proposed. The rapid carbonation of alkaline metal ions and the efficient solidification of heavy metal ions were achieved in the wet grinding carbonation. After 40 min of short-term carbonation, the CO2 uptake and carbonation degree of SRM reached 30.25 g CO2/100 g SRM and 79.31% respectively. The high-efficiency CO2 uptake of SRM was attributed to the continuous stripping of the attached surface CaCO3 layer by wet grinding, the constantly exposed new surface area after refinement and the largely increased Ca2+ concentration, which was 12.5 times the initial value at 10 min. Furthermore, the simultaneous carbonation realized the solidification of dissolved chromium ion (Cr(III)/Cr(VI)), which was transformed into CaCrO4, Ca3Cr2(OH)12 or Cr(OH)n(CO3)n(3n-3)- complexes under the weak acid environment of CO2. After 40 min of wet grinding carbonation, the Cr concentration was notably decreased by 85.71 %, which was lower than the limit of groundwater standard requirement.

Broadband near-infrared emission in barium gallo-germanate glasses co-doped with bismuth, chromium and erbium ions

This work presents barium gallo-germanate glasses co-doped with Bi+/Er3+ and Cr3+/Er3+ ions for NIR luminescence. The addition of Al2O3 content in the glass matrix made it possible to obtain luminescence corresponding to the 3P1→3P0 transition of Bi+ ions. Co-doping with the Bi+/Er3+ system resulted in a broad luminescence spectrum of 1.0-1.6 µm and Cr3+/Er3+ co-doping in selected glass matrix resulted in luminescence in 0.9-1.6 µm band. However, the luminescence of the Cr3+ ions is much lower than that of Er3+ ions. Full Text: PDF References T. Suzuki, G.S. Murugan, and Y. Ohishi, 'Optical properties of transparent Li2O-Ga2O3-SiO2 glass-ceramics embedding Ni-doped nanocrystals', Appl. Phys. Lett., 86(13), 131903 (2005). CrossRef N.V. Golubev et al., 'Pre-crystallization heat treatment and infrared luminescence enhancement in Ni2+-doped transparent glass-ceramics', J. Non-Cryst. Solids, 515, 42 (2019) CrossRef Z. Xu, W. Feng, T. Chen, X. Liu, and J. Qiu, 'Tuning optical properties in PbSe quantum dot-doped borosilicate glass fiber by modulation of network topology', Opt. Laser Technol., 158, 108910 (2023). CrossRef M.A. Hughes, T. Suzuki, and Y. Ohishi, 'Spectroscopy of bismuth-doped lead-aluminum-germanate glass and yttrium-aluminum-silicate glass', J. Non-Cryst. Solids, 356(44), 2302 (2010). CrossRef J. Song, Z. Zhou, B. Zhong, M. Zhang, J. Huang, and L. Han, 'Ultra-broadband near-infrared Cr3+-doped multi-phase glass-ceramics realized by the selective enrichment strategy for near-infrared spectroscopy applications', J. Alloys Compd., 968, 172126 (2023). CrossRef M.A.U. Martines, M.R. Davolos, M.J. Júnior, D.F. de Souza, and L.A.O. Nunes, 'Cr3+ and Cr4+ luminescence in glass ceramic silica', J. Lumin., 128(11), 1787 (2008). CrossRef S. Zhou, H. Dong, H. Zeng, J. Hao, J. Chen, and J. Qiu, 'Infrared luminescence and amplification properties of Bi-doped GeO2−Ga2O3−Al2O3 glasses', J. Appl. Phys., 103(10), 103532 (2008). CrossRef T. Suzuki and Y. Ohishi, 'Ultrabroadband near-infrared emission from Bi-doped Li2O-Al2O3-SiO2 glass', Appl. Phys. Lett., 88(19), 191912 (2006). CrossRef T. Minh Hau et al., 'Super broadband near-infrared emission and energy transfer in Bi-Er co-doped lanthanum aluminosilicate glasses', Opt. Mater., 35(3), 487 (2013). CrossRef H.K. Dan et al., 'Effects of Y3+on the enhancement NIR emission of Bi+-Er3+ co-doped in transparent silicate glass-ceramics for Erbium-doped fiber amplifier (EDFA)', J. Lumin., 219, 116942 (2020). CrossRef E.M. Dianov, 'Bismuth-doped optical fibers: a challenging active medium for near-IR lasers and optical amplifiers', Light Sci. Appl., 1(5) (2012). CrossRef L. Wang, L. Tan, Y. Yue, M. Peng, and J. Qiu, 'Efficient Enhancement of Bismuth NIR Luminescence by Aluminum and Its Mechanism in Bismuth‐Doped Germanate Laser Glass', J. Am. Ceram. Soc., 99(6), 2071 (2016). CrossRef Z. Jiang et al., 'Effects of Al2O3 composition on the near-infrared emission in Bi-doped and Yb-Bi-codoped silicate glasses for broadband optical amplification', J. Non-Cryst. Solids, 383, 196 (2014). CrossRef

Metal Ion Release in Cancer Patients Following Megaprosthesis Salvage Surgery

BackgroundMegaprostheses contain many more modular components than conventional total hip and knee arthroplasty, which may lead to higher serum levels of metal ions. The aim of this study was to determine serum concentrations of titanium, chromium, and cobalt ions in cancer patients after limb salvage surgery with a megaprosthesis. MethodsA retrospective, descriptive cohort analysis consisting of patients who underwent cancer-related limb salvage surgery with a megaprosthesis at our hospital between 2010 and 2020 was conducted. Baseline and follow-up data were extracted from clinical and surgical records. Blood samples were prospectively obtained. Descriptive statistics were used for the analysis. ResultsA total of 71 patients underwent limb salvage surgery during the study period. Of these, 22 (10 women, 12 men) were included in the study. The mean age was 52 years (range, 21 to 80). Most cases (n = 16; 72.7%) involved the femur. Most patients (n = 14, 63.6%) underwent total knee megaprosthesis surgery. Implant revision surgery was required in 45% of cases (n = 10), with a mean interval of 4.32 years between the initial and revision surgeries. The mean follow-up time after revision surgery was 4.05 years. High levels of chromium were observed in 22.7% of patients (n = 5). High cobalt levels were found in 68.2% (n = 15) of patients, with toxic levels in 9.1% (n = 2). Titanium levels were high in 77.3% (n = 17) of cases and toxic in 22.7% (n = 5). Postoperative chemotherapy was significantly associated with titanium levels (P = .017). No correlation was observed between metal ion levels and time from primary or revision surgery or time from the first to revision surgery. ConclusionsThis study shows that cancer-related limb salvage surgery with megaprosthesis is associated with metal ion levels that exceed established safe thresholds. Compared to conventional hip arthroplasty, a higher proportion of the patients in this cohort presented elevated levels of metal ions. Level of evidenceIII.

Green synthesis of iron nanoparticles using Pistacia-atlantica leaf extract for enhanced removal of Cr(VI) from aqueous solution

The discharge of chromium-containing wastewater from various industries into aqueous environments is regarded as an important and challengeable matter due to its high toxicity. The application of conventional methods for eliminating this pollutant are often very expensive and difficult. Therefore, the adsorption process has been introduced as a desirable and effective method for removing chromium ions from aqueous media. In this research, iron nanoparticles (Fe-NPs) were synthesized using Pistacia-atlantica leaf extract as a reducing agent, then they were characterized by DLS, XRD, FT-IR, FESEM/EDS, and TEM techniques and its effectiveness to eliminate hexavalent chromium (Cr (VI)) from aqueous solutions was carried out. The capability of the batch adsorption procedure was assessed under different operational factors, such as initial pH, adsorbent dose and initial Cr (VI) concentration. Optimum adsorption conditions were determined at initial pH of 2, Cr (VI) concentration of 25 mg L−1 and adsorbent dose of 0.24 g L−1. Based on the obtained results, the highest removal efficiency (99.9%) by the adsorption process was occurred at pH of 2, concentration of 5 mg L−1 and 30 min of operational time. On the other hand, the results showed that the percentage of the pollutant elevated by increasing the contact time and amount of adsorbent dose, whereas that of was declined by increasing the initial concentration of Cr (VI). Besides, the experimental equilibrium data was evaluated by Langmuir, Freundlich, and Temkin isotherm models, and the outcomes revealed conformity with the Langmuir isotherm model. The Cr (VI) adsorption utilizing Fe-NPs adhered to a pseudo-first-order kinetic model. Eventually, thermodynamic studies demonstrated that the adsorption of Cr (VI) onto the surface of the Fe-NPs is endothermic and spontaneous.

Targeted Redox Balancing through Pulmonary Nanomedicine Delivery Reverses Oxidative Stress Induced Lung Inflammation.

Non-invasive delivery of drugs is important for the reversal of respiratory diseases essentially by-passing metabolic pathways and targeting large surface area of drug absorption. Here, we study the inhalation of a redox nano medicine namely citrate functionalized Mn3O4 (C-Mn3O4) duly encapsulated in droplet evaporated aerosols for the balancing of oxidative stress generated by the exposure of Chromium (VI) ion, a potential lung carcinogenic agent. Our optical spectroscopic in-vitro experiments demonstrates the efficacy of redox balancing of the encapsulated nanoparticles (NP) for the maintenance of a homeostatic condition. The formation of Cr-NP complex as an excretion of the heavy metal is also demonstrated through optical spectroscopic and high resolution transmission optical microscopy (HRTEM). Our studies confirm the oxidative stress mitigation activity of the Cr-NP complex. A detailed immunological assay followed by histopathological studies and assessment of mitochondrial parameters in pre-clinical mice model with chromium (Cr) induced lung inflammation establishes the mechanism of drug action to be redox-buffering. Thus, localised delivery of C-Mn3O4 NPs in the respiratory tract via aerosols can act as an effective nanotherapeutic agent against oxidative stress induced lung inflammation.

NaY zeolite synthesis from rice husk ash for Chromium(VI) ion adsorption

NaY zeolite in this study is novelly synthesized from rice husk ash with a one-stage process instead of passing the solid silica recovery process as usual. NaY zeolite applies to assess adsorption ability of chromium(VI) ions in water with varying key factors. The as-synthesized zeolite is characterized by X-ray diffraction, X-ray fluorescence, scanning electron microscope, specific surface area analysis and inductively coupled plasma mass spectrometry with optical emission spectroscopy. As a result, the optimal conditions for silica extraction are at 90oC with a NaOH concentration of 4 M for 4 h with recovery efficiency 87.5%. NaY zeolite is successfully synthesized with Si/Al ratio of 10, aging time of 24 h and crystallization time of 24 h with synthesis yield of 31.25% and crystallinity of 96%. The optimal conditions for the chromium(VI) adsorption in aqueous solution are at pH 2.0, adsorption time of 120 min, initial concentration of 20 mg/L with an adsorbent mass of 0.1 g. The kinetics and adsorption isotherms show a good agreement with pseudo-second order and Freundlich adsorption isotherm model. NaY zeolite is synthesized via environmentally friendly approach with time and energy savings and shows its high adsorb-ability of chromium(VI) in water.

Tris buffer-accelerated ligand exchange rate for instant fluorescence detection of trivalent chromium ion

Functional nucleic acids (FNAs) have attracted a lot of attention for the rapid detection of metal ions. Cr3+ is one of the major heavy metal ions in natural waters. Due to the slow ligand exchange rate of Cr3+, the FNA-based Cr3+ sensors require long assay times, limiting the on-site applications. In this study, we report that the good's buffers containing amino and polyhydroxy groups greatly increase the ligand exchange rate of Cr3+. Using EDTA as a model coordinate ligand, the Tris buffer (100 mM, pH 7.0) showed the best acceleration effect among the eight buffers. It improved the rate constant ∼20-fold, shorten the half-time 19-fold, and lowered the activation energy ∼70% at 40 °C. The Tris buffer was then applied for sensor based on the Cr3+-binding induced fluorescence quenching of fluorescein (FAM)-labeled and single-stranded DNA (ssDNA), which shortened the assay time from 1 h to 1 min. The Tris buffer also ∼100% enhanced the fluorescence intensity of FAM, achieving the 11.4-fold lower limit of detection (LOD = 6.97 nM, S/N = 3). By the combination use of the Tris buffer and ascorbic acid, the strong interference from Cu2+, Pb2+, and Fe3+ suffered in many previous reported Cr3+ sensors was avoided. The practical application of the sensor for the detection of Cr3+ spiked in the real water samples were demonstrated with high recovery percentages. The Tris buffer could be applied for other metal ions with slow ligand exchange rate (such as V2+, Co3+ and Fe2+) to solve diverse issues such as long assay time and low synthesis yield of metal complexes, without the need of heating treatment.

Power benefitted bioremediation of hexavalent chromium ions in biochar blended soil microbial fuel cell

Power benefitted bioremediation of hexavalent chromium ions in biochar blended soil microbial fuel cell

Synthesis, XPS and NEXAFS spectroscopy study of Zn, Cr codoped bismuth tantalate pyrochlores

The study investigated the formation of inhomophase ceramics through Zn doping in Bi2СrTa2O9.5–Δ. It was found that all Bi2ZnxCr1–xTa2O9.5–Δ (0.3 ≤ x ≤ 0.7) investigated samples crystallized in the pyrochlore structural type (sp. Gr. Fd-3m) and contained an admixture of triclinic β-BiTaO4 (up to 24 wt %, sp. gr. P-1), with the admixture concentration proportional to the degree of zinc doping. It was shown that impurities in the samples could be eliminated by creating a defective bismuth sublattice proportional to the impurity content, resulting in single-phase Bi2–yZnxCr1–xTa2O9.5–Δ (y ≤ 0.5, 0.3 ≤ x ≤ 0.7) samples with the pyrochlore structure. The unit cell parameter of pyrochlore increased with an increase in zinc ion content in the samples from 10.4493 Å (x = 0.3) to 10.4976 Å (x = 0.7). The microstructure of ceramics was represented by individual slightly melted grains 0.5–2 μm in size, which increased in size and fuse with each other with an increase in zinc content. The near edge X-ray absorption fine structure (NEXAFS) and X-ray photoelectron spectroscopy (XPS) data showed that zinc doping did not change the oxidation degree of bismuth and tantalum in pyrochlore, with the ions in charge states Bi(+3), Zn(+2) and Ta(+5). The study also observed an energy shift of the absorption band in the Ta 4f spectrum toward lower energies (ΔE = 0.55 eV) characteristic of tantalum ions with an effective charge (+5–δ) and a shift of the Bi 4f7/2 and Bi 4f5/2 bands shift to lower energies with increase in x(Zn), due to the distribution of some Zn(II) ions in the bismuth position. The oxidation degree of chromium ions in the samples was mainly (+3), with some chromium ions oxidized and having an oxidation degree close to (+6) according to NEXAFS data. The studied ceramics showed promise as dielectrics for multilayer ceramic capacitors and devices for microwave applications due to their low sintering temperature and high porosity.

Trivalent chromium ion doping garnet phosphor with broadband near-infrared emission for night-vision applications

Trivalent chromium ion doping garnet phosphor with broadband near-infrared emission for night-vision applications

Green redox separation and efficient extraction of vanadium and chromium from leaching solution of chrome-vanadium slag

Green separation and efficient extraction of vanadium and chromium from vanadium-chromium leaching solution are serious challenges for the utilization of chrome-vanadium slag. A green sucrose reduction-H2O2 selective oxidation route is proposed for deep separation of vanadium and chromium from vanadium-chromium leaching solution based on different redox properties. Eh-pH diagram of V-Cr-H2O system and existence forms of vanadium and chromium ions are calculated. Obvious difference of redox properties between V(V) and Cr(VI) exists in acidic environment. The dependences of selective separation on pH for reduction, temperature, m(sucrose)/m(Cr(VI)) and n(H2O2)/n(V(V)) are studied. The concentration ratio of vanadium to chromium in solution after selective separation of chromium decreases from 1.6 to 0.06. The extraction ratios of Cr2O3 and V2O5 are 96.3% and 93.8%, respectively. The redox behavior of V(V) and Cr(VI) is revealed. Cr(VI) and V(V) are reduced to Cr(Ⅲ) and V(IV) by 5-hydroxymethylfurfural, a hydrolysate of sucrose, and then V(IV) is selectively oxidized to V(V) by H2O2. Cr2O3·n(H2O) and ammonium polyvanadate obtained by hydrolysis and ammonium precipitation are calcined to Cr2O3 and V2O5, respectively. Cr2O3 with the purity of 99.4% can be used as high-quality pigment. The purity of V2O5 meets the requirements of YB/T 5304–2011 for 98 V2O5.

Solidification/Stabilization of Chromium-Contaminated Soils by Polyurethane during Freeze-Thaw Cycles: Mechanical, Leaching and Microstructure Characterization.

The treatment of chromium-contaminated soil in seasonal frozen soil areas has been the subject of recent interest. Polyurethane (PU), as a polymer material with excellent freeze-thaw resistance and abrasion resistance, has the potential to solidify Chromium-Contaminated soil in seasonal frozen soil areas. However, there is a lack of research on the mechanism of PU involved in solidifying/stabilizing chromium-contaminated soil in seasonal frozen regions from the perspective of pore structure and functional group coordination bonds. In this study, the leaching behavior of PU with different contents under different freeze-thaw cycles was analyzed, and the mechanism of PU in seasonal frozen regions was explored from the perspective of pores and functional groups by combining various microscopic characterization methods. The results show that PU can effectively resist the deterioration of chromium-contaminated soil after freeze-thaw cycles and can better prevent the harm of secondary leaching. The leaching concentration of chromium ion is only 1.09 mg/L, which is below China's regulatory limits. PU is beneficial for inhibiting the expansion of ice crystals in chromium-contaminated soil in seasonal frozen soil areas. PU solidifies chromium by physical encapsulation and complexation reactions. The amide functional groups, methyl-CH3 and isocyanate groups in PU play a leading role in the complexation with chromium. Although the freeze-thaw cycle will destroy the coordination bond between the PU functional group and chromium, chromium cannot break through the bond of PU film. This study confirmed the feasibility of using PU to solidify Chromium-Contaminated soil in seasonal frozen soil areas, which can provide research support and reference for in situ engineering in the future.

Adsorption of lead and chromium ions from electroplating wastewater using plantain stalk modified by amorphous alumina developed from waste cans

Waste beneficiation is key to environmental protection and the realisation of a circular economy. Herein, amorphous alumina (a-Al2O3) derived from aluminium waste cans (AWC) was used to modify plantain stalk as an adsorbent for sequestration of lead (II) and chromium (VI) ions from electroplating wastewater. Raw plantain-stalk (RPS) and amorphous-alumina modified plantain stalk (APS) developed as adsorbents were characterised using various equipment such as x-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET). The FTIR revealed that the adsorbents are rich in functional groups that could promote the adsorption process which includes carboxyl, hydroxyl, and aliphatic groups. Also, the BET analysis showed a substantial increase in the surface area of APS (174.448 m2/g) compared to that of RPS (40.531 m2/g) which could be due to the effect of modification by the a-Al2O3. The batch adsorption studies revealed that the APS achieved 99.38% and 98.33% removal of Cr(VI) and Pb(II), respectively, which is superior to RPS adsorption efficiency. Also, the estimated and experimental data for the APS compared well under all the kinetic models studied with R2 > 0.88. This suggested that chemisorption is the most plausible adsorption mechanism of Cr(VI) and Pb(II) onto the APS. Further analysis showed that the Cr(VI) and Pb(II) adsorption followed the Langmuir model with the RL value of 0.038 and 0.999, respectively, which indicated that the two metal ions were effectively adsorbed onto the APS. Therefore, this work demonstrated that the modification of plantain-stalk with amorphous-alumina derived from AWC enhanced the characteristics of the APS and favoured its adsorption of the selected heavy metals.

Investigation on the valence state stability and optical properties of Mg2GeO4:Cr

In this work, the valence states and optical properties of chromium-doped Mg2GeO4 are investigated via first-principles methods. The formation energies and thermal charge transition levels show that the site occupation and valence states of chromium are strongly related to the growth condition: Cr3+ dominates in the Mg sites under Mg-poor conditions, and Cr4+ dominates in the Ge sites under Ge-poor conditions. With the lithium co-doping, the Fermi-level is pinned below the midgap, and the formation energies of chromium-doped Mg sites become the lowest either Mg-poor or Ge-poor conditions, suggesting that the co-doping of lithium ions promotes the chromium to preferentially occupy Mg sites, in good agreement with experiments. Furthermore, the excitation and emission processes of chromium ions are investigated, and our results recommend that the near-infrared emission is related to the 4T2 to 4A2 transition of Cr3+ at the Mg sites and the infrared emission is related to the 3T2-3A2 transition of Cr4+ at the Ge site. Our results help to understand the stability of the valence states of chromium ions doped Mg2GeO4 and the effects of ions co-doping in regulating the chromium valence states, as well as the corresponding optical properties of different types of chromium ions.

Humic acid-nanoceria composite as a sustainable adsorbent for simultaneous removal of uranium(VI), chromium(VI), and fluoride ions from aqueous solutions.

In this article, the multifunctional behavior of novel, efficient, and cost-effective humic acid-coated nanoceria (HA@CeO2 NPs) was utilized for the sorptive removal of U(VI), Cr(VI), and F- ions at different conditions. The production cost of HA@CeO2 was $19.28/kg and was well characterized by DLS, FESEM, HRTEM, FTIR, XRD, XPS, and TGA. Batch adsorption study for U(VI) (at pH ~ 8), Cr(VI) (at pH ~ 1), and F- (at pH ~ 2) revealed that the maximum percentage of sorption was > 80% for all the cases. From the contact time experiment, it was concluded that pseudo-second-order kinetics followed, and hence, the process should be a chemisorption. The adsorption study revealed that U(VI) and Cr(VI) followed the Freundlich isotherm, whereas F- followed the Langmuir isotherm. Maximum adsorption capacity for F- was 96mgg-1. Experiments in real water suggest that adsorption is decreased in Kaljani River water (~ 12% for Cr(VI) and ~ 11% for F-) and Kochbihar Lake water (25.04% for Cr(VI) and 20.5% for F-) because of competing ion effect. Mechanism was well established by the kinetic study as well as XPS analysis. Because of high adsorption efficiency, HA@CeO2 NPs can be used for the removal of other harmful water contaminants to make healthy aquatic life as well as purified drinking water.