Metal Ion Concentration Research Articles

Inhibition sensitivity of invitro firefly bioluminescence quantum yields to Zn2+ and Cd2+ concentrations in aqueous solutions.

To elucidate the inhibition effects of Zn2+ and Cd2+ on the luciferin-luciferase reaction, we performed quantitative measurements of quantum yields and spectral shapes for invitro firefly bioluminescence in aqueous solutions containing ZnSO4, ZnCl2, CdSO4, and CdCl2 at different concentrations. Particular care was taken toward the equilibrium between metal ions and enzyme proteins, anion difference, solubility, and uncertainty evaluation. The bioluminescence quantum yields decreased almost linearly to the concentration of Zn2+ and Cd2+ below 0.25 mM. No obvious difference was found between the chloride and sulfate anion solutions. We defined inhibition sensitivity as the decrease in relative quantum yield versus the concentration of metal ions, and they were determined to be 1.48 ± 0.13 and 1.13 ± 0.16/mM for Zn2+ and Cd2+, respectively. We estimated the detection limit of inhibition effects as the concentration of metal ions that decrease relative quantum yields by 10%, which were 0.07 mM (4 ppm) and 0.09 mM (10 ppm) for Zn2+ and Cd2+, respectively. The shape of the bioluminescence spectra changed sensitively with the increase in Zn2+ concentrations. The bioluminescence peak energy for 0.10-mM Zn2+ was ~2.2 eV, while that for 0.25-mM Zn2+ was ~2.0 eV. The shape of the spectra changed less sensitively with the increase in Cd2+concentrations, and the peak energy was at ~2.2 eV for Cd2+ concentrations of 0.10 and 0.25 mM.

Competitive adsorption behavior and adsorption mechanism of limestone and activated carbon in polymetallic acid mine water treatment

Acid mine water (AMD) can cause significant environmental hazards due to its high concentration of metal ions, so the development of effective treatment methods is essential to mitigate its impact. In this study, adsorption experiments were conducted using limestone (LS) and activated carbon (AC) to explore the adsorption efficiency for different concentrations of metal ions. Adsorption was evaluated by static and competitive batch tests. The adsorbent mechanism was investigated using analytical techniques such as SEM, FTIR and XRD. The efficacy of LS and AC for competitive adsorption of Fe, Mn, Zn and Cu ions from AMD was evaluated. The study analyzed the effect of environmental conditions such as initial concentration and ionic strength on the adsorption efficiency. The results showed that LS showed high adsorption capacity for Fe and Cu, but was less effective in competitive adsorption of Mn. AC showed superior adsorption performance for Fe and Cu under competitive conditions due to its high surface area and functional groups. Both adsorbents showed selective efficacy influenced by the physicochemical properties of metal ions. This study helps to guide the optimization of adsorbents in AMD treatment and highlights the importance of selecting suitable materials based on specific metal ion properties.

Harnessing Moringa oleifera root powder (MORP) for the sustainable remediation of heavy metal contaminated water.

Heavy metal environmental pollution is rapidly increasing due to the increase in industrialization and urbanization. Industrial processes, such as paint production, mining, and raw materials producing industries release effluents rich in heavy metals, like Pb2+, Cd2+, Cu2+, and Cr3+. These heavy metals are dangerous because they persist in nature, are non-biodegradable and they have high tendency to accumulate in the environment and in living organisms who are exposed to them. This work studied the removal of heavy metals (Cu, Pb, Cr, and Cd) from aqueous solution using Moringa oleifera root powder (MORP) as the adsorbent. The MORP was characterized by SEM, FTIR, BET, and XRD. Batch adsorption experiments carried out investigated the effects of adsorbate concentration, adsorbent dosage, agitation time, pH and temperature on adsorption. The optimum parameters are: contact time (90 min); pH (9); adsorbent dose (0.6); metal ion concentration (30 mg L-1) for Cr and 40 mg L-1 for the rest; and temperature (50 °C) for Cu and Pb, and 70 °C for Cr and Cd. These experimental data were analyzed with 5 isotherm models (Temkin, Flory-Huggins, Langmuir, D-R and Freundlich). The result obtained fitted best to Temkin isotherm in comparison to others. Kinetic studies revealed that the pseudo-second order kinetic model best described the adsorption (with high R2 values ranging from 0.9810-0.9976) compared to pseudo-first order and intra-particle diffusion kinetics model. Results of the thermodynamic study showed that the sorption process was endothermic for Cu and Pb, but exothermic for Cd and Cr. The adsorbent showed good adsorptive tendencies toward the ions studied, and could be applied on an industrial scale for the remediation of metal contaminated water.

In situ synthesis of Chitin/ZIF-67 composite hydrogel for efficient recovery of high purity acetonitrile by removal of Zn2+ and Ag+

The improper disposal of waste high purity acetonitrile (HPA) not only causes environmental degradation but also poses significant risks to human health. One of the major challenges in the recycling and reuse of waste HPA is the removal of trace metal ions. In this study, we successfully fabricated a chitin/ZIF-67 composite hydrogel (CZ-n) by one pot in situ synthesis method for the purification and recovery of waste HPA for the first time. ZIF-67 was embedded into chitin through hydrogen bonding and coordination and provided more active adsorption sites, which resulted in CZ-3 with higher adsorption capacity than CZ-0. The maximum adsorption capacities of CZ-3 for Zn2+ and Ag+, as determined by fitting the Langmuir model, were 85.46 mg·g-1 and 91.26 mg·g-1, respectively. CZ-3 was able to effectively decrease the metal ion (Zn2+ and Ag+) concentration to below 10 ppb within 24 h through a monolayer adsorption process using chelation. Furthermore, the adsorption capacity remained satisfactory even in the presence of an equivalent concentration of NaCl, and CZ-3 exhibited remarkable reusability, with a removal rate exceeding 80 % after five cycles. Additionally, it also displayed notable biodegradability, with complete degradation observed within 60 days. These results indicated that CZ-3 could be a potential absorbent in the purification and recovery of waste HPA.

Heat and mass transfer performance of multi-solute electroplating wastewater in spray evaporation separation process

Electroplating wastewater is complex in composition and contains many harmful substances. Based on the single droplet heat and mass transfer method, a one-dimensional mathematical model for the evaporation separation heat and mass transfer process of multi-solute electroplating wastewater is established. In order to validate the model, the experimental system of evaporation separation tower is established, and Nusselt numbers corresponding to metal ion solutions are fitted, reliabilities of models are also verified. The maximum relative errors of mathematical models are within 10.0 %. In addition, effects of the type and concentration of metal ions and air inlet temperature on heat and mass transfer characteristics of spray separation tower are investigated. Experimental results show that when the wastewater inlet concentration is the same, the improvement effects of increasing air inlet temperature on evaporation and separation performance from high to low are ZnCl2, CuCl2, and NiCl2 solutions. When the air inlet temperature increases from 90 °C to 130 °C, the evaporation speed of ZnCl2, CuCl2 and NiCl2 solutions increase by 90.3 %, 84.3 % and 45.7 %, respectively. When the air inlet temperature is the same, with the increase of wastewater inlet concentration, the evaporation separation performance of electroplating wastewater in descending order is ZnCl2, CuCl2, and NiCl2 solutions.

Waste tea as absorbent for removal of heavy metal present in contaminated water

The goal of this study is to investigate the efficacy of tea-derived absorbents for the removal of heavy metals from contaminated water. For this, absorbents were prepared from milk tea (MT) waste, Ilam tea (IT) waste, and various types of tea leaves, including Immature (IML), mature (ML), and old leaves (OL). The characterization of the absorbents revealed distinct physical and chemical properties from X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR), with varying degrees of effectiveness observed across different absorbent types. Heavy metal removal efficiency was assessed using a chemical-free UV-spectrophotometer. The results show that the maximum removal efficiency for Cd using the IT absorbent reaches up to 82.14 % with 100 ppm cetyltrim ethylammonium bromide (CTAB), while the minimum removal efficiency is 32.14 % using the OL absorbent with 20 ppm CTAB. For Zn, the OL absorbent demonstrates a maximum removal efficiency of 52.59 % with 100 ppm CTAB, whereas the minimum efficiency is 3.70 % using the ML absorbent with 20 ppm CTAB. For Ni, the highest removal efficiency is achieved with the ML absorbent, reaching up to 97.73 % with 100 ppm CTAB, and the lowest is 31.82 % with the MT absorbent with 20 ppm CTAB. The addition of a catalyst further enhanced removal efficiencies in both absorbents and metals. Also, the removal of heavy metal ions using 0.05 g of tea absorbent combined with CTAB at varying concentrations. Results show that the addition of 20 ppm and 100 ppm CTAB significantly reduces metal ion concentrations from an initial 100 mg/L. The metal ion concentration decreases as CTAB concentration increases, demonstrating the effectiveness of CTAB in enhancing the absorption capacity of tea absorbent for heavy metal removal. The investigation of selective adsorption of Ni, Zn, and Cd by an adsorbent, revealing competitive adsorption behavior with Ni and Zn being adsorbed more rapidly than Cd, suggesting the impact of metal ion interference on adsorption efficiency. However, limitations were observed with certain absorbent types; for instance, immature leaves did not effectively remove Ni. Overall, this study underscores the potential of tea-derived absorbents as sustainable solutions for mitigating heavy metal pollution in industrial wastewater. Further research is needed to optimize absorbent formulations and explore their applicability in real-world environmental remediation scenarios.

Volatile fatty acid release and metal ion concentration in hydrothermal carbonization liquid

Volatile fatty acid release and metal ion concentration in hydrothermal carbonization liquid

Catalytic effect of the in-situ rhodium(III) complexes in surfactant medium on the auto-oxidation of 1,2-hydroxyphenylthiourea: A theoretical and experimental study for rhodium(III) sensing

1,2-hydroxyphenylthiourea(HPTU) undergoes auto-oxidation to form an yellow colored dimer. The process of auto-oxidation is enhanced by the presence of trace quantities of transition metal ions and transition metal complexes that act as catalysts. In the current study, catalytic potential of rhodium(III) complexes on the auto-oxidation of 1,2-hydroxyphenylthiourea(HPTU) was studied theoretically using quantum mechanical calculations and experiments were carried out using photometry and fluorometry. DFT studies inferred that [Rh(Py)6]Cl3 showed a better catalytic activity in the dimerization of HPTU. Theoretical studies were subsequently validated through experiments using photometric methods and the range of detection was determined to be 6 ng/mL–100 ng/mL. The detection limit was observed to be 2 ng/mL. Analytical parameters such as pH, reagent concentration, metal ion concentration, appropriate activators and surfactants were established.

A deep treatment process for chemical polishing wastewater towards resource recovery: Optimization and performance

The chemical polishing industry generates abundant wastewater that contains high concentrations of phosphoric acid and metal ions. In light of the rapid growth of the economy and the stringent demands for sustainability, developing cost-effective and energy-efficient technologies for wastewater treatment is crucial. Herein, an EPRC-ICT-ANT process integrating electrodialysis, iron contact, and alkali neutralization, was proposed to deeply treat chemical polishing wastewater and achieve optimal recovery of acid, phosphorus, and aluminum. The results indicated that with the electrochemical phosphoric acid recovery cell (EPRC), the maximum recovery efficiency and final phosphoric acid concentration were 34.6 % and 25.2 g/L. Following the iron contact tank and alkali neutralization tank (ICT-ANT) treatment, a remarkable 99.17 % removal of Al3+ and 49.5 kg/t wastewater yield of AlPO4 were achieved. Simultaneously, the released Fe2+ and remaining PO43- triggered the rapid formation of vivianite with a yield of 120.7 kg/t wastewater. This comprehensive treatment strategy led to the near-complete removal of Al3+ and PO43- (∼100 %) with an impressive recovery of Al3+ (∼100 %) and PO43- (75.7 %), emphasizing its immense potential for chemical polishing wastewater treatment.

WITHDRAWN: Studies on decontamination of cadmium rich water by a novel nano Iron oxide adsorbent

Synthesizing non-toxic adsorbent for abatement of hazardous pollutants from water is important to develop safe environment. In this study, nanocrystalline iron oxide particles were synthesized and utilized as effective nanoadsorbent for removing cadmium through adsorption. The as-prepared nanoadsorbent was characterized using sophisticated techniques. The objective of this study was to improve cadmium adsorption from aqueous solutions under a variety of conditions. With the help of Box-Behnken design, adsorption parameter settings were improved. Response Surface Methodology analysis was conducted to optimize the adsorption conditions, including pH, initial concentration of metal ions, and adsorbent dose. Comparisons were made between the optimal equations for linear and non-linear kinetics, along with isotherm models. Origin's curve fitting tool and the Solver add-in of Microsoft Excel are two non-linear analytical tools. The obtained results showed that the Origin curve fitting tool is superior to solver add in's error analysis method for determining isotherm parameters. The equilibrium data for cadmium removal using nano iron oxide/hydroxide adsorbent was best fitted to Langmuir isotherm model. The adsorption of cadmium was well described by the pseudo-second-order model. The study shows that the system appears to be spontaneous according to the Langmuir constant method and thermodynamic parameter via partition.

Pollution and Potential Ecological Risk Assessment of Heavy Metals in Water Bodies in the Vicinity of Industrial Zones

This research was undertaken to determine the concentrations of heavy metal ions in the surface water and sediment in water bodies that receive wastewater from the Dinh Tram and Pho Noi A industrial zones. The pollution status of the heavy metal ions and their potential ecological risks were evaluated by using the potential ecological risk index (RI) and risk assessment code (RAC). The results showed that some metal ions, namely Fe3+, Ni2+, and Pb2+, exceeded the allowed standards of QCVN 08:2023/BTNMT. The sediments were polluted by Zn2+, As2+, Cr6+, and Fe3+ at concentrations 2.4, 3.7, 1.9, and 2.0 times higher, respectively, than the QCVN 43:2017/BTNMT. The potential ecological risk indices for the heavy metal ions were in order as: (As2+) = 7.94 > (Cd2+) = 3.68 > (Cr6+) = 3.39 > (Pb2+) = 2.73 > (Cu2+) = 2.74 > (Zn2+) = 2.4 (T6 channel) and (As2+) = 11.1 > (Cd2+) = 7.74 > (Cu2+) = 2.64 > (Cr6+) = 2.31 > (Pb2+) = 1.9 > (Zn2+) = 0.87 (Bun River). The risk assessment code (RAC) ranged from 0.17 to 39.42 (T6 channel) and from 0.03 to 38.96 (Bun River). The RAC-based risk assessment results showed that both the T6 channel and Bun River presented a medium risk for Cd2+, a low risk for Mn2+, Zn2+, Cu2+, and Ni2+, and no risk for the remaining metals, Cr6+, Pb2+, As2+, and Fe3+. These results were caused by the differences in environmental quality assessments between using separate parameters versus biological risk assessments.

Influence of pyrolysis time on removal of heavy metals using biochar derived from macroalgal biomass (Oedogonium sp.)

In this study, pyrolysis was performed at different times to convert Oedogonium biomass into biochar. The physicochemical properties show that the pyrolysis time significantly impacts structural and morphological changes in biochar samples. The influence of pyrolysis time on the removal of multiple heavy metals was investigated. Owing to the presence of abundant functional groups, inorganic minerals and porous nature, biochar obtained from a 40 min pyrolysis time showed higher removal efficiency of heavy metals compared to biochars pyrolyzed at 20 mins and 60 mins even with higher concentrations of metal ions. The maximum adsorption capacity was observed 9.33, 10.74, 322.58, 13.70 and 9.11 mg/g with the biochar prepared at the pyrolysis time of 40 mins for Co, Ni, Cu, Zn and Cd, respectively. The adsorption isotherm is well fitted with the Langmuir adsorption model for heavy metals adsorption, and the kinetic study is well-defined by a pseudo second-order model.

Liquid-liquid extraction of selenium (IV) ions from hydrochloric acid solution using Aliquat 336 dissolved in kerosene.

Solvent extraction of selenium(IV) ions from highly concentrated hydrochloric acid using 0.4mol/L Aliquat 336 dissolved in kerosene was investigated. As a modifying agent, 1-octanol (10% v/v) was added to the organic phase to avoid the third phase formation. The effect of different parameters affecting the liquid-liquid extraction of selenium(IV) such as the acid concentration, shaking time, metal ion concentration in the aqueous phase, loading capacity, diluents, and temperature, was studied. The results indicate that selenium(IV) is extracted efficiently by 0.4mol/L Aliquat 336 dissolved in kerosene. It was noticed that the extraction increased with the increase in the acid and Aliquat 336 concentrations, reaching an extraction percentage of about 92% at 8mol/L HCl and 97.1% at 1mol/L extractant. The extracted organic species is postulated to be [H2SeO2Cl2.2R4NCl]org by using the slope analysis method, and the value of Kex for selenium(IV) extraction was found to be 26.17 ± 2 M- 2. The structure of the extracted organic species was confirmed by FT-IR. The effect of diluents using various aliphatic and aromatic diluents indicated that kerosene is the most preferred diluent. This is owing to safety ground purpose, economic consideration, the lower cost, availability, and lower toxicity. Thermodynamic parameters indicate the endothermic nature for the solvent extraction of selenium(IV) for the investigated system according to the positive value obtained of the enthalpy change (ΔH). Depending on the obtained results, the method was used to recover selenium(IV) from a simulated solution synthesized in hydrochloric acid medium, which is expected in anode slime leach liquor solution.

Adsorptive potential of dispersible chitosan-coated biogenic iron oxide nanocomposite for enhanced anti-bacterial activity against gram-positive and gram-negative bacterial pathogens

The use of various biomaterials, such as plants or microbes, to create nanoparticles (NPs), is seen as a viable strategy in green nanotechnology. The synthesis of low-cost, energy-efficient, nontoxic, ecologically acceptable metallic nanoparticles has recently become a critical topic. The biosynthesis of iron oxide NPs using pomegranate peel extract has been investigated. Biogenic iron oxide NPs were coated with highly porous chitosan as a supporting material to enhance applicability of NPs for wastewater remediation. Biogenic magnetic NPs and its composite were characterized by scanning electron microscope, X-ray diffraction, and Fourier Transformer Infrared spectroscopy (FTIR). Our study focused on the ability of biogenic magnetite Fe3O4 NPs and its bio-composite for removal of As+5 ions from wastewater. Adsorption isotherms were obtained using metal ion concentrations ranging from 5 to 25 mg/L. The Langmuir adsorption model was validated by our data. The reaction kinetics of the adsorption process were pseudo-second order. Interestingly, the bio-composite achieved 90% As+5 removal at pH4. In addition, the prepared nanocomposite was characterized using various analytical techniques to confirm its physicochemical properties. The adsorptive capacity of the nanocomposite was evaluated by studying the removal of pollutants and contaminants from aqueous solutions. Additionally, the antibacterial activity of the nanocomposite was assessed against a panel of clinically relevant Gram-positive and Gram-negative bacterial strains, including Staphylococcus epidermidis (RCMB 9241, ATCC 12228), Staphylococcus saprophyticus (RCMB 010028, ATCC 15305), Enterococcus faecalis (RCMB 010052), Streptococcus salivarius (ATCC 13415), Escherichia coli (RCMB 010052, ATCC 25922), Salmonella enterica serovar Typhimurium (RCMB 006(1), ATCC 14028) and Pseudomonas aeruginosa (ATCC 27853). Our findings have important implications in the field of low-cost, easy, and environmentally friendly water bioremediation.

Batch and column studies for the removal of basic red-46 dye and textile by using magnesium oxide (MgO), strontium titanium trioxide (SrTiO3), cobalt- and iron-doped lanthanum chromium trioxide (Co.Fe.LaCrO3), and cadmium sulfide (CdS)-doped graphene oxide nanocomposites.

Despite efforts to reduce the risk of toxic chemicals, colors, and dyes being released into the environment from urban and industrial areas, there is still cause for concern. Colored water must be filtered and sterilized before it can be used for irrigation. The utilization of metal oxide and nanocomposite materials in wastewater treatment procedures appears to be a viable option for the future. Therefore, different compounds were doped with graphene oxide to identify the best material for dye removal by the adsorption process. According to recent studies, the ideal conditions for graphene oxide-doped magnesium oxide (GO/MgO) are as follows: pH 10 showed the highest adsorption capacity (qe) at 49.4mg/g; an adsorbent dosage of 0.01g/50mL showed 48.3mg/g qe; a shaking time of 30min resulted in 44.2mg/g qe; an initial dye concentration of 100mg/L yielded 53.6mg/g qe; and a temperature of 35°C gave 49.5mg/g qe. For graphene oxide-doped strontium titanate (GO/SrTiO3), the optimum conditions were as follows: pH 10 with 45.8mg/g qe; an adsorbent dose of 0.01g/50mL with 40.5mg/g qe; a shaking time of 30min with 75mg/g qe; and a temperature of 35°C with 44.7mg/g qe. Graphene oxide-doped cobalt and iron-doped lanthanum chromium titanate (GO/Co.Fe.LaCrO3) showed optimum conditions of pH 9 with 34.2mg/g qe; an adsorbent dose of 0.01g/50mL with 27.5mg/g qe; a shaking time of 45min with 33.2mg/g qe; an initial dye concentration of 100mg/L with 37.6mg/g qe; and a temperature of 35°C with 42.5mg/g qe. Graphene oxide-doped cadmium sulfide (GO/CdS) showed the following optimum conditions: pH 8 with 23.1mg/g qe; an adsorbent dose of 0.01g/50mL with 25.5mg/g qe; an initial dye concentration of 75mg/L with 28.3mg/g qe; and a temperature of 35°C with 33.5mg/g qe. The pseudo-first-order model was the best fit only for graphene oxide-doped magnesium oxide (GO/MgO) with an R2 value of 0.966, while the pseudo-second-order adsorption isotherm was the best fit for all four products, with R2 values ranging from 0.991 to 0.998. Additionally, the Langmuir adsorption isotherms provided good results for all four products, with R2 values ranging from 0.957 to 0.985. The Freundlich adsorption kinetics showed satisfactory fit only for graphene oxide-doped magnesium oxide (GO/MgO) and graphene oxide-doped cadmium sulfide (GO/CdS), with R2 values of 0.951 and 0.982, respectively. To examine the characteristics and practicality of the adsorption process, certain thermodynamic variables were calculated. The adsorption capability of the most efficient nanocomposites for the degradation of basic red-46 was significantly affected by various concentrations of heavy metal ions and electrolytes. In dye solutions containing surfactants/detergents, the adsorption efficiency of several effective photocatalysts for basic dyes was significantly reduced. A 0.5M HCl solution was found to be the most effective for desorption. In column investigations, the optimal bed height, flow velocity, and dye intake levels were determined to be 3cm, 1.8mL/min, and 70mg/L, respectively, for maximal adsorption of basic red-46. The adsorption investigation of genuine textile waste products has also been carried out to facilitate the practical deployment of this approach. The methods used in this study were cost-effective, easy to handle, and eco-friendly and involved no hazardous materials in the synthesis, making the resulting materials non-hazardous. All these methods were part of green chemistry.

Efficient synthesis of salidroside from tyrosol based on UDPG recycling system

Salidroside is a functional ingredient with wide applications in food and pharmaceutical fields. It is conventionally produced by extraction from plants, the application of which is limited by the scarcity of raw materials and cumbersome process. This study achieved the efficient production of salidroside by biosynthesis with tyrosol as the substrate. While utilizing glycosyltransferases for tyrosol glycosylation, we introduced sucrose synthase to construct the uridine diphosphate glucose (UDPG) recycling system. The glycosyltransferase UGT33 and sucrose synthase AtSUS were screened out by comparison, and the recombinant strain Escherichia coli BL21/pETDuet-AtSUS-UGT33 was constructed. The copy number of the gene was optimized and the optimal copy number ratio of glycosyltransferase to sucrose synthase was determined to be 3:1. The whole-cell transformation conditions (temperature, pH, inoculum amount, substrate concentration, and concentrations of metal ions) of the recombinant strain were optimized, and the highest yield of salidroside reached 8.17 g/L after fermentation under the optimal conditions in a 5 L fermenter for 24 h. This study provides a reference for the efficient production of salidroside by microorganisms.

Synthesis and Characterization of Low-Cost Zirconium Nanocomposites as Novel Adsorbents for Arsenazo III Pollutant

Removing contaminated Arsenazo III dye from contaminated effluent is a challenge and of great interest due to its hazard and environmental impact. Therefore, the biggest challenge was producing highly efficient, easy to recycle, and economically inexpensive adsorbent materials for the contaminated dye. Three chemically stable zirconium nanocomposites with unique properties were synthesized by gel-precipitation technology. The composition, chemical, and physical properties of zirconium molybdate, tungstate, and silicate nanocomposites have been extensively proven using many different and appropriate devices such as XRD, SEM–EDX, TEM, FT-IR, BET, DLS, TGA-DTA, and zeta potential. By utilizing the most effective adsorption techniques, Azo-dye was successfully bound to ZrMo-NPs, ZrW-NPs, and ZrSi-NPs composites. The uptake capacities for these composites were measured at 0.29, 0.79, and 1.61 mmol.g−1, respectively. The sorption parameters were optimized as follows: a feed solution pH of 3 for ZrMo-NPs, a pH of 2.3 for ZrW-NPs, and a pH of 2.3 for ZrSi-NPs. The stirring time was set at 30 min, the metal ion concentration was 1.64 mmol L−1, and the sorbent dose was 7.5 mg. The adsorption results agreed well with the Langmuir isotherm and the pseudo-second-order reaction models and demonstrated the endothermic nature and kinetic improvement by increasing temperatures. The three nanocomposites effectively eliminated tainted dye from lab wastewater, offering promise for their potential applications in the future.Graphical

Green synthesis of platinum nanoparticles using aqueous bark extract of Quercus sp. for potential antioxidant and antimicrobial applications

Oak bark, which is commonly used in the wood industry, has by-products often repurposed as fuel. Its extracts are rich in compounds with anticancer, antibacterial, antifungal, and anti-inflammatory properties. This study synthesized platinum nanoparticles (PtNPs) using aqueous extracts from Quercus dalechampii (QD), Q. frainetto (QF), and Q. petraea (QP). Key factors during nanoparticle formation included reaction time, metal ion concentration, pH, extract-to-metal ion ratio, and temperature. The PtNPs were characterized by dynamic light scattering, Fourier transform infrared spectroscopy, and transmission electron microscopy. The average diameters were 58.5 ± 7.6 nm for QD-PtNPs, 41.6 ± 5.4 nm for QF-PtNPs, and 41 ± 5.3 nm for QP-PtNPs. Antioxidant and antimicrobial activities were also analyzed. The QP-PtNPs had the highest DPPH (2,2-Diphenyl-1-picrylhydrazyl), FRAP (Ferric Reducing Antioxidant Power), and CUPRAC (Cupric Reducing Antioxidant Capacity) free radical scavenging activities, while QD-PtNPs excelled in ABTS (2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)) scavenging. All PtNPs showed strong antimicrobial properties, particularly against Enterococcus faecalis, Escherichia coli, Candida krusei, and Candida auris. These findings suggest that Quercus-mediated PtNPs have significant potential for developing treatments against bacterial and fungal infections, with promising applications in medicine.

Reversible in situ Control over Monolayer Organization.

Cr2+ and Cr3+ ions are shown to mediate the formation, morphology, and organization of arachidic acid (AA) Langmuir-Blodgett (LB) monolayers. This finding, based on cyclic voltammetry (CV), linear sweep voltammetry (LSV) and fluorescence recovery after photobleaching (FRAP) measurements, show that Langmuir monolayer formation depends on subphase pH and metal ion concentration. Following monolayer deposition on indium tin oxide (ITO), the LB monolayer organization can be modified reversibly through control of the Cr oxidation state, which has not been shown before by other monolayers formed with other divalent metal ions. The dynamics and the mobility of a chromophore (perylene) incorporated into the monolayer sense changes in Cr oxidation state-dependent organization of the LB monolayer. Demonstrating reversible changes in monolayer organization provides an opportunity to control chemical and electron access to the interface support.

Impact of Metal Ions on Cellular Functions: A Focus on Mesenchymal Stem/Stromal Cell Differentiation.

Metals play a crucial role in the human body, especially as ions in metalloproteins. Essential metals, such as calcium, iron, and zinc are crucial for various physiological functions, but their interactions within biological networks are complex and not fully understood. Mesenchymal stem/stromal cells (MSCs) are essential for tissue regeneration due to their ability to differentiate into various cell types. This review article addresses the effects of physiological and unphysiological, but not directly toxic, metal ion concentrations, particularly concerning MSCs. Overloading or unbalancing of metal ion concentrations can significantly impair the function and differentiation capacity of MSCs. In addition, excessive or unbalanced metal ion concentrations can lead to oxidative stress, which can affect viability or inflammation. Data on the effects of metal ions on MSC differentiation are limited and often contradictory. Future research should, therefore, aim to clarify the mechanisms by which metal ions affect MSC differentiation, focusing on aspects such as metal ion interactions, ion concentrations, exposure duration, and other environmental conditions. Understanding these interactions could ultimately improve the design of biomaterials and implants to promote MSC-mediated tissue regeneration. It could also lead to the development of innovative therapeutic strategies in regenerative medicine.