Search Results (10)

Hexavalent chromium (Cr(VI)) is a high-priority environmental pollutant due to its strong oxidizing properties, which cause DNA damage and other severe health effects. Conventional detection methods are often costly and lack real-time monitoring capabilities, creating a strong demand for cost-effective, real-time biosensors that meet industrial requirements. In this study, we developed a novel biosensor for continuous Cr(VI) monitoring using a single-chamber microbial fuel cell (MFC). The biological element is an engineered Escherichia coli strain (ChrA-ChrB-E. coli), constructed by introducing Cr(VI)-resistant (ChrA) and Cr(VI)-reducing (ChrB) genes. The presence of Cr(VI) affects bacterial metabolism and electron transfer within the MFC, generating a measurable signal proportional to the contaminant’s concentration. The biosensor demonstrated robust performance and characteristics. The recombinant strain retained functional activity after 450 days of storage at −20 °C. The system exhibited high sensitivity and excellent linearity (R² ≥ 0.999) across a broad Cr(VI) concentration range of 0.015–200 mg/L. During continuous monitoring of chrome tanning and electroplating wastewater, measurements deviated by less than 2.33% from the standard diphenylcarbazide (DPC) method; electroplating deviation was further reduced to −0.69% with EDTA pretreatment. In fishery water, the deviation was higher (−7.12%) due to dissolved oxygen (DO) interference but was reduced to −0.75% after mechanical stirring to remove DO. The biofilm bacterial community remained highly stable over six months in both wastewater types, with the inoculated ChrA-ChrB-E. coli strain maintaining dominance (>99.6%). These results substantiate the feasibility of using this biosensor for continuous, online, real-time detection of Cr(VI) in actual wastewater environments. Full article

The tanning of hides is a practice deeply rooted in ancient times, but in the early 20th century, transitioning to an industrial model of leather and hide production, chrome tanning expanded globally due to its practicality, quality, and versatility. However, in recent decades, there has been a growing attention paid to the potential oxidation of the free chromium present in tanned leather, which could transform from an unharmful trivalent status into its carcinogenic hexavalent status. This phenomenon occurs in a very small fraction of hides, which is yet sufficient to exhibit significant activity. Hence, there is an evident need to explore further alternatives that allow avoiding oxidation. In this work, the performance of a sequence of selected antioxidants is evaluated in different oxidation conditions: simple stirring, UV–Vis–IR irradiation, and heating up to 75 °C. The official diphenylcarbazide–UV tool norm was used to quantify the hexavalent chromium amount. The results underline the effectiveness of 2,6-di-tert-butylphenol, and that its greatest preventative method of addition during the tanning process is together with the tanning agent. This approach will pave the way for researching alternative concepts and exploring perspectives to inhibit chromium issues. Full article

A reliable, rapid, and low-cost procedure for determining very low concentrations of hexavalent chromium (Cr) in water is discussed. The procedure is based in the classical reaction of Cr⁶⁺ with diphenylcarbazide. Once this reaction has taken place, sodium dodecylsulfate is added to obtain an ion-pair, and Triton X-114 is incorporated. Next, the heating of the mixture allows two phases that can be separated by centrifugation to be obtained in a cloud point microextraction (CPE) process. The coacervate contains all the Cr⁶⁺ originally present in the water sample, so that the measurement by molecular absorption spectrophotometry allows the concentration of the metal to be calculated. No harmful organic solvents are required. The discrimination of hexavalent and trivalent forms is achieved by including an oxidation stage with Ce⁴⁺. To take full advantage of the pre-concentration effect inherent to the coacervation process, as well as to minimize reagent consumption and waste generation, a portable mini-spectrophotometer which is compatible with microvolumes of liquid samples is used. The preconcentration factor is 415 and a chromium concentration as low as 0.02 µg L⁻¹ can be detected. The procedure shows a good reproducibility (relative standard deviation close to 3%). Full article

Cr(VI) is highly soluble and mobile in water solution and extremely toxic. In order to obtain a specific material with adsorption properties towards Cr(VI), and that can be used in environmental remediation of water contaminated with Cr(VI), one-step sol-gel technique, at low temperature (50 °C), has been optimized to prepare transparent silica-based xerogel monolith by using tetraethyl orthosilicate as precursor. The obtained xerogel, with disk shape, was fully characterized by Raman, BET, FE-SEM and XRD analysis. The results indicated that the material showed silica amorphous phase and high porosity. The study of the adsorption properties towards different concentrations of Cr(VI), in the form of HCrO₄⁻ in acidic condition, showed prominent results. The absorption kinetics were evaluated by studying different models, the final result showing that the absorption of Cr(VI) occurred through intra-particle diffusion process, following two steps, and that the absorption equilibrium is regulated by Freundlich isotherm model. The material can be restored by reducing the hazardous Cr(VI) to Cr(III), a less toxic form of chromium, by 1,5-diphenylcarbazide, and with successive treatment in acidic water. Full article

Coconut oil as a natural solvent is proposed for green downscaling solvent extractive determination. Determination of Cu(II) using 1,5-Diphenylcarbazide (DPC) was selected as a model for the investigation. Cu(II)-DPC complexes in aqueous solution were transferred into coconut oil phase. The change of the color due to Cu(II)-DPC complexes in coconut oil was followed by using a smartphone and image processing. A single standard concept was used for a series of Cu(II) standard solutions. A downscaling procedure using a 2 mL vial provided a calibration: color intensity = −142 [Cu(II)] + 222, (R² = 0.98), 10% RSD. Using a well plate, a calibration was: color intensity = 61 [Cu(II)] + 68 (R² = 0.91), 15% RSD. Both were for the range of 0–1 ppm Cu(II). Application of the developed procedure to water samples was demonstrated. The developed procedures provided a new approach of green chemical analysis. Full article

Hexavalent chromium (Cr (VI)) ion, as highly toxic environmental pollution, severely endangers the ecological environment and public health. Herein, a fluorescent nanosensor (PFO-DPC) was constructed by combining semiconducting polymer dots with diphenylcarbazide (DPC) for sensing Cr (VI) ion in aqueous solution and living cells. DPC and poly (styrene-co-maleic anhydride) (PSMA) polymer mixed with polyfluorene (PFO) were utilized for selectively indicating Cr (VI) ion and improving the efficiency of detection, respectively. The presence of Cr (VI) ion effectively turned off the blue and green fluorescence of PFO-DPC in the aqueous environment, and the fluorescence quenching efficiency exhibited a good linear relationship between the range of 0.0 to 2.31 nM (R² = 0.983) with a limit of detection (LOD) of 0.16 nM. The mechanism of fluorescence quenching could possibly be attributed to the internal filtration effect (IFE). Additionally, PFO-DPC showed a satisfactory performance in monitoring intracellular Cr (VI) ion. Our results indicate that the sensor is promising in various applications. Full article

A flow-based method for the spectrophotometric determination of chromium (VI) in recreational waters with different salinities was developed. Chromium can occur in the environment in different oxidation states with different related physiological properties. With regard to chromium, the speciation is particularly important, as the hexavalent chromium is considered to be carcinogenic. To achieve that purpose, the use of the diphenylcarbazide (DPC) selective colored reaction with the hexavalent chromium was the chosen strategy. The main objective was to develop a direct and simple spectrophotometric method that could cope with the analysis of different types of environmental waters, within different salinity ranges (fresh to marine waters). The potential interference of metal ions, that can usually be present in environmental waters, was assessed and no significant interferences were observed (<10%). For a complete Cr(VI) determination (three replicas) cycle, the corresponding reagents consumption was 75 µg of DPC, 9 mg of ethanol and 54 mg of sulfuric acid. Each cycle takes about 5 min, including the system clean-up. The limit of detection was 6.9 and 12.2 µg L⁻¹ for waters with low and high salt content, respectively. The method was applied for the quantification of chromium (VI) in both fresh and marine water, and the results were in agreement with the reference procedure. Full article

Among chemical water pollutants, Cr(VI) is a highly toxic heavy metal; solar photocatalysis is a cost-effective method to reduce Cr(VI) to innocuous Cr(III). In this research work, an efficient and economically feasible ZnO/CuO nanocomposite was grafted onto the polyester fabric ZnO/CuO/PF through the SILAR method. Characterization by SEM, EDX, XRD, and DRS confirmed the successful grafting of highly crystalline, solar active nanoflakes of ZnO/CuO nanocomposite onto the polyester fabric. The grafting of the ZnO/CuO nanocomposite was confirmed by FTIR analysis of the ZnO/CuO/PF membrane. A solar photocatalytic reduction reaction of Cr(VI) was carried out by ZnO/CuO/PF under natural sunlight (solar flux 5–6 kW h/m²). The response surface methodology was employed to determine the interactive effect of three reaction variables: initial concentration of Cr(VI), pH, and solar irradiation time. According to UV/Vis spectrophotometry, 97% of chromium was removed from wastewater in acidic conditions after four hours of sunlight irradiation. ZnO/CuO/PF demonstrated reusability for 11 batches of wastewater under natural sunlight. Evaluation of Cr(VI) reduction was also executed by complexation of Cr(VI) and Cr(III) with 1, 5-diphenylcarbazide. The total percentage removal of Cr after solar photocatalysis was carried out by AAS of the wastewater sample. The ZnO/CuO/PF enhanced the reduction of Cr(VI) metal from wastewater remarkably. Full article

The photoproduction of superoxide anion radical (O₂^−•) and hydrogen peroxide (H₂O₂) in photosystem II (PSII) preparations depending on the damage to the water-oxidizing complex (WOC) was investigated. The light-induced formation of O₂^−• and H₂O₂ in the PSII preparations rose with the increased destruction of the WOC. The photoproduction of superoxide both in the PSII preparations holding intact WOC and the samples with damage to the WOC was approximately two times higher than H₂O₂. The rise of O₂^−• and H₂O₂ photoproduction in the PSII preparations in the course of the disassembly of the WOC correlated with the increase in the fraction of the low-potential (LP) Cyt b₅₅₉. The restoration of electron flow in the Mn-depleted PSII preparations by exogenous electron donors (diphenylcarbazide, Mn²⁺) suppressed the light-induced formation of O₂^−• and H₂O₂. The decrease of O₂^−• and H₂O₂ photoproduction upon the restoration of electron transport in the Mn-depleted PSII preparations could be due to the re-conversion of the LP Cyt b₅₅₉ into higher potential forms. It is supposed that the conversion of the high potential Cyt b₅₅₉ into its LP form upon damage to the WOC leads to the increase of photoproduction of O₂^−• and H₂O₂ in PSII. Full article

Chromium contamination of drinking water has become a global problem due to its extensive use in industry. The most commonly used methods for chromium detection in water are laboratory-based methods, such as atomic absorption spectroscopy and mass spectroscopy. Although these methods are highly selective and sensitive, they require expensive maintenance and highly trained staff. Therefore, there is a growing demand for cost effective and portable detection methods that would meet the demand for mass monitoring. Microfluidic detection systems based on optical detection have great potential for onsite monitoring applications. Furthermore, their small size enables rapid sample throughput and minimises both reagent consumption and waste generation. In contrast to standard laboratory methods, there is also no requirement for sample transport and storage. The aim of this study is to optimise a colorimetric method based on 1,5-diphenylcarbazide dye for incorporation into a microfluidic detection system. Rapid colour development was observed after the addition of the dye and samples were measured at 543 nm. Beer’s law was obeyed in the range between 0.03–3 mg·L⁻¹. The detection limit and quantitation limit were found to be 0.023 and 0.076 mg·L⁻¹, respectively. Full article