Search

Chromium (Cr), due to its greater contamination in aquifers and distinct eco-toxic impacts, is of greater environmental concern. This study aimed to synthesize nanocomposites of almond shells biochar (BC) with zerovalent bismuth and/or copper (Bi0/BC, Cu0/BC, and Bi0–Cu0/BC) for the removal of Cr from aqueous solution. The synthesized nanocomposites were investigated using various characterization techniques such as XRD, FTIR spectroscopy, SEM, and EDX. The Cr removal potential by the nanocomposites was explored under different Cr concentrations (25–100 mg/L), adsorbent doses (0.5–2.0 g/L), solution pH (2–8), and contact time (10–160 min). The above-mentioned advanced techniques verified successful formation of Bi0/Cu0 and their composite with BC. The synthesized nanocomposites were highly effective in the removal of Cr. The Bi0–Cu0/BC nano-biocomposites showed higher Cr removal efficiency (92%) compared to Cu0/BC (85%), Bi0/BC (76%), and BC (67%). The prepared nanocomposites led to effective Cr removal at lower Cr concentrations (25 mg/L) and acidic pH (4.0). The Cr solubility changes with pH, resulting in different degrees of Cr removal by Bi0–Cu0/BC, with Cr(VI) being more soluble and easier to adsorb at low pH levels and Cr(III) being less soluble and more difficult to adsorb at high pH levels. The experimental Cr adsorption well fitted with the Freundlich adsorption isotherm model (R2 > 0.99) and pseudo-second-order kinetic model. Among the prepared nanocomposites, the Bi0–Cu0/BC showed greater stability and reusability. It was established that the as-synthesized Bi0–Cu0/BC nano-biocomposite showed excellent adsorption potential for practical Cr removal from contaminated water. [ABSTRACT FROM AUTHOR]

Batch scale removal of arsenic (As) from aqueous media was explored using nano-zero valent iron (Fe0) and copper (Cu0) particles. The synthesized particles were characterized using a Brunauer-Emmett–Teller (BET) surface area analyzer, a scanning electron microscope (SEM), and Fourier transform infrared spectroscopy (FTIR). The BET result showed that the surface area (31.5 m2/g) and pore volume (0.0415 cm3/g) of synthesized Fe0 were higher than the surface area (17.56 m2/g) and pore volume (0.0287 cm3/g) of Cu0. The SEM results showed that the morphology of the Fe0 and Cu0 was flowery microspheres and highly agglomerated with thin flakes. The FTIR spectra for Fe0 showed broad and intense peaks as compared to Cu0. The effects of the adsorbent dose (1–4 g/L), initial concentration of As (2 mg/L to 10 mg/L) and solution pH (2–12) were evaluated on the removal of As. Results revealed that effective removal of As was obtained at pH 4 with Fe0 (94.95%) and Cu0 (74.86%). When the dosage increased from 1 to 4 g L−1, the As removal increased from 70.59 to 93.02% with Fe0 and from 67 to 70.59% with Cu0. However, increasing the initial As concentration decreased the As removal significantly. Health risk indices, including estimated daily intake (EDI), hazard quotient (HQ), and cancer risk (CR) were employed and a significant decline (up to 99%) in risk indices was observed in As-treated water using Fe0/Cu0. Among the adsorption isotherm models, the values of R2 showed that isothermal As adsorption by Fe0 and Cu0 was well explained by the Freundlich adsorption isotherm model (R2 > 0.98) while the kinetic experimental data was well-fitted with the Pseudo second order model. The Fe0 showed excellent stability and reusability over five sorption cycles, and it was concluded that, compared to the Cu0, the Fe0 could be a promising technology for remediating As-contaminated groundwater. [ABSTRACT FROM AUTHOR]

Binary composite of zerovalent iron and titanium dioxide (Fe0/TiO2) was synthesized for the catalytic removal of dichlorophene (DCP) in the presence of peroxymonosulfate (PMS). The as-prepared composite (Fe0/TiO2) exhibits synergistic effect and enhanced properties like improved catalytic activity of catalyst and greater magnetic property for facile recycling of catalyst. The results showed that without addition of PMS at reaction time of 50 min, the percent degradation of DCP by TiO2, Fe0, and Fe0/TiO2 was just 5%, 11%, and 12%, respectively. However, with the addition of 0.8 mM PMS, at 10 min of reaction time, the catalytic degradation performance of Fe0, TiO2, and Fe0/TiO2 was significantly improved to 82%, 18%, and 88%, respectively. The as-prepared catalyst was fully characterized to evaluate its structure, chemical states, and morphology. Scanning electron microscopy results showed that in composite TiO2 causes dispersion of agglomerated iron particles which enhances porosity and surface area of the composites and X-ray diffraction (XRD), energy dispersive X-ray (EDX), and Fourier-transform infrared (FTIR) results revealed successful incorporation of Fe0, and oxides of Fe and TiO2 in the composite. The adsorption–desorption analysis verifies that the surface area of Fe0/TiO2 is significantly larger than bare Fe0 and TiO2. Moreover, the surface area, particle size, and crystal size of Fe0/TiO2 was surface area = 85 m2 g−1, particle size = 0.35 μm, and crystal size = 0.16 nm as compared to TiO2 alone (surface area = 22 m2 g−1, particle size = 4.25 μm, and crystal size = 25.4 nm) and Fe0 alone (surface area = 65 m2 g−1, particle size = 0.9 μm, and crystal size = 7.87 nm). The as-synthesized material showed excellent degradation performance in synthesized wastewater as well. The degradation products and their toxicities were evaluated and the resulted degradation mechanism was proposed accordingly. The toxicity values decreased in order of DP1 > DP5 > DP2 > DP3 > DP4 and the LC50 values toward fish for 96-h duration decreased from 0.531 to 67.2. This suggests that the proposed technology is an excellent option for the treatment of antibiotic containing wastewater. [ABSTRACT FROM AUTHOR]

In this work, bismuth-doped titania (BixTiO2) with improved oxygen vacancies was synthesized by sol-gel protocol as a novel peroxymonosulfate (PMS, HSO5−) activator. HSO5− and adsorbed oxygen molecules could efficiently be transformed into their respective radicals through defect ionization to attain charge balance after their trapping on oxygen vacancies of the catalyst. XRD study of BixTiO2 with 5 wt% Bi (5BiT) revealed anatase, crystalline nature, and successful doping of Bi into TiO2 crystal lattice. The particle size obtained from BET data and SEM observations was in good agreement. PL spectra showed the formation rates of •OH by 3BiT, 7BiT, 5BiTC, and 5BiT as 0.720, 1.200, 1.489, and 2.153 μmol/h, respectively. 5BiT catalyst with high surface area (216.87 m2 g−1) and high porosity (29.81%) was observed the excellent HSO5− activator. The catalytic performance of 0BiT, 3BiT, 5BiT, and 7BiT when coupled with 2 mM HSO5− for recalcitrant flumequine (FLU) removal under dark was 10, 27, 55, and 37%, respectively. Only 5.4% decrease in catalytic efficiency was observed at the end of seventh cyclic run. Radical scavenging studies indicate that SO4•− is the dominant species that caused 62.0% degradation. Moreover, strong interaction between Bi and TiO2 through Bi-O-Ti bonds prevents Bi leaching (0.081 mg L−1) as shown by AAS. The kinetics, degradation pathways, ecotoxicity, and catalytic mechanism for recalcitrant FLU were also elucidated. Cost-efficient, environment-friendly, and high mineralization recommends this design strategy; BixTiO2/HSO5− system is a promising advanced oxidation process for the aquatic environment remediation. [ABSTRACT FROM AUTHOR]

Globally, a large number of school-aged children is suffering from water-borne diseases, particularly in low-income countries. Arsenic (As) is a hazardous and potentially carcinogenic metal(loid) in drinking water. Nowadays, alarming levels of As have been reported in the groundwater of Vehari District, Punjab Pakistan. In this study, drinking water supplies for high and higher secondary schools were examined in Vehari District. A total of 164 water samples were collected from schools and subjected to heavy metal(loid) analysis (As) and basic water physicochemical parameters. The results were analyzed with respect to sampling area, school type, school education level, sources of sample collection, and the depth of the source. The results revealed that As concentration of water samples in boys' and girls' schools was 12.8 μg/L and 9.2 μg/L, respectively. However, when the As concentration in drinking water was evaluated at the school education level, a notable higher concentration of As was observed in the higher secondary schools than the high schools with an average of 19.5 and 9.7 μg/L, respectively. The risk assessment indices were calculated based on education level and different age groups of the children (primary, elementary, high, and higher secondary). High carcinogenic (cancer risk = 0.001) and non-carcinogenic (hazard quotient = 2.0) risks were noted for the children in higher secondary school. The current findings anticipated that the drinking water of schools in Vehari District did not meet the requirement of the World Health Organization (WHO) drinking water quality guidelines. Safe drinking water is crucial for the development and growth of children. Therefore, it is important for educational authorities to take steps for provision of As free safe drinking water to students and local inhabitants. [ABSTRACT FROM AUTHOR]

In the current investigation, a new insight into the adsorptive interaction of iron–silicon mixed oxide with arsenate was proposed through comparative studying the behavior of arsenate on the mixed oxide and on the parent oxides, i.e., iron hydroxide and silica. All the oxides were characterized by using different physiochemical methods. The arsenate concentration, pH, temperature, co-ion effect, and calcination of adsorbents were the key parameters of this investigation. The Langmuir model was used for the interpretation of the adsorption data. The thermodynamic parameters and spectroscopic evidences of the samples before and after arsenate adsorption confirmed that the mechanisms of arsenate adsorption by Fe(OH)3 and mixed oxide showed close similarity. [ABSTRACT FROM AUTHOR]

In this study, for the first-time, aqueous solution of Acid Fuchsin (AF) was spectrophotometrically evaluated as a possible chemical dosimeter for food irradiation dosimetry at low dose ranges. A 50 µM solution of AF at natural pH was gamma irradiated and absorbance of the solution was measured at λmax (i.e., 543 nm) in addition to other wavelengths (490, 510, 549 and 564 nm). The response of AF dosimeter was investigated by plotting various variables, i.e., absorbance (A), − log A, change in absorbance (∆A), log Ao/Ai and absorbance % (A %) against absorbed dose. The response plots suggested that the beneficial dose range of AF solution in water was up to 0.82 kGy when absorbance (A), change in absorbance (ΔA) and absorbance % (A %) were extrapolated against absorbed dose. Though, the response was linear and beneficial absorbed dose range was extended up to 1.65 kGy, when − log A and log Ao/Ai were plotted against absorbed dose. It was concluded from pre- and post-irradiation stability studies of AF dosimeter that it should be protected from light and heat during handling and storage. For detection of the reactive specie involved in the bleaching of AF dye the AF dye solution was saturated with O2, N2 and N2O gases. [ABSTRACT FROM AUTHOR]

Soil contamination with heavy metals is a global issue confronting the environmental pollution and human/animal health. Much work has been done on physiological and antioxidant responses of wheat in hydroponic experiments and health risks from individual heavy metal contamination to human, but limited information is available on their combined application in soil. Therefore, this pot study delineates the uptake of lead and cadmium, as well as physiological responses of wheat and associated health risks under different levels of alone and combined Cd and Pb treatments. Metal uptake increased with their increasing applied levels. The highest Cd (4.24, 1.38, and 0.92 mg kg−1) and Pb (763.33, 39.63, and 16.35 mg kg−1) concentrations in root, shoot, and grain, respectively, were observed at highest applied levels (0.4 mM Cd and 10 mM Pb). Furthermore, all the treatments increased lipid peroxidation and activities of superoxide dismutase, catalase, ascorbate peroxidase, and peroxidase, while decreased total chlorophyll contents and membrane stability index. Under combined application of Cd and Pb, the toxicity and detoxification responses of wheat increased compared to alone treatments. Multivariate analysis further confirmed the toxicity and accumulation pattern of metals under alone and combined treatments. Target hazard quotient values of Cd and Pb were < 1 under alone and combined treatments. The health hazard index values of Pb (97.07 and 87.89%) were higher than those of Cd (2.93 and 12.10%) in combined application for human and buffalo, respectively. This study highlights that the multi-metal contamination (Cd and Pb) is detrimental for wheat growth and human/animal health. [ABSTRACT FROM AUTHOR]