Untreated wastewater is a risk factor for the spread of antibiotic resistance in the environment. However, little is known about the contribution of untreated wastewater to the burden of antibiotic resistance in the Nigerian environment. In this study, a total of 143 ceftazidime-/cefpodoxime-resistant bacteria isolated from untreated wastewater and untreated wastewater-contaminated surface and groundwater in Nigeria were screened for extended-spectrum β-lactamase (ESBL) genes, integrons and integron gene cassettes by PCR. The genetic environment of bla CTX₋M₋₁₅ was mapped by PCR and potentially conjugative plasmids were detected among the isolates by degenerate primer MOB typing (DPMT). ESBL production was confirmed in 114 (79.7%) isolates and ESBL genes (bla SHV, bla CTX₋M₋₁₅ and bla TEM) were detected in 85 (74.6%) ESBL-producing isolates. bla CTX₋M₋₁₅ was associated with ISEcp1 and with orf477 in 12 isolates and with ISEcp1, IS26 and orf477 in six others. To the best of our knowledge, this is the first report of bla CTX₋M₋₁₅ in hand-dug wells and borehole serving as sources of drinking water and a first report of the genetic environment of bla CTX₋M₋₁₅ in environmental bacteria from Nigeria. The results of this study confirm untreated wastewater as an important medium for the spread of ESBL-producing bacteria within the Nigerian environment. Hence, the widespread practice of discharging untreated wastewater into the aquatic ecosystem in Nigeria is a serious risk to public health.

The aim of this study was to investigate the concentrations of five essential (Fe, Mn, Zn, Cu and Se) and four non-essential/toxic elements (Cr, Cd, Ni and Pb) in 35 different starter infant formulas (0–6 months) sold in Italy. In addition, a safety assessment of these trace elements was carried out, by comparing the estimated daily intake (EDI) with the adequate intake (AI) and the provisional tolerable daily intake (PTDI), with a view to provide information on the metal distribution patterns and health risk to infants arising from the consumption of these products. The concentrations were determined by using inductively coupled plasma mass spectrometry after microwave digestion. The concentrations expressed in geometric mean ± geometric standard deviation of Fe (6.17 ± 1.61 mg/L), Zn (6.21 ± 1.31 mg/L), Cu (416.4 ± 1.21 μg/L), Mn (121.5 ± 1.85 μg/L) and Se (13.27 ± 1.67 μg/L) were within legal limits. In spite of this, the mean EDIs of Fe (4.81 mg/day) and Mn (94.75 μg/day) were many times higher than the recommended AI, especially for Mn. Chromium, Ni, Cd and Pb concentrations were not detectable in 11, 37, 57 and 66% of the samples, respectively. Considering the overall sample, the GM ± GSD of these elements were 4.80 ± 5.35 μg/L for Cr, 1.02 ± 11.65 μg/L for Ni, 0.21 ± 14.83 μg/L for Cd and 0.14 ± 17.13 μg/L for Pb. The mean EDIs were far below the respective PTDI. When the safety assessment was based on the 75° percentile level of each elements, all EDIs remained well below the PTDI, with the exception of Cd, whose EDI approached (74.7%), albeit remaining below the PTDI. In conclusion, our results and the increased awareness on the potential risks of excessive Mn and Fe for infants support that an urgent scientific-based definition of the appropriated levels of fortification in formulas is required. Moreover, regular monitoring of all the stages of production of infant formulas is essential in order to limit toxic metal contamination.

The application or disposal of char derived from tannery sludge is directly influenced by the mobility and bioavailability of Cr during pyrolysis process. This study focused on the changes of Cr speciation and organic matter in tannery sludge during low-temperature pyrolysis (100–400 °C) to evaluate the toxicity of char in terms of the leaching possibility of Cr. The results showed that (1) lower char yield and more porous structure were observed after pyrolysis. (2) Higher pyrolysis temperature increased Cr content in the char; however, Cr in this case was converted into the residual fraction which minimized its bioavailability therefore lowers its potential risk to the environment. (3) Organic matters in the acid and alkali leachates were mainly humic acid-like substance, and condensed organic matter might appear at 200 °C and then destruct. (4) Despite the comparatively high content of Cr in the char, the leaching toxicity of char was within the security range according to the national standard of China. The Cr content in the acid and alkali leachates decreased to the range of 16.5–35.3 and 0.2–6.8 mg/L, respectively. It was suggested that the potential toxicity of tannery sludge from Cr could be reduced before utilization or disposal by pyrolysis, especially under 400 °C.

One of the most important features of photocatalytic materials intended to be used for water treatment is their long-term stability. The study is focused on the application of thermal and chemical treatments for the reactivation of TiO₂-SnS₂ composite photocatalyst, prepared by hydrothermal synthesis and immobilized on the glass support using titania/silica binder. Such a catalytic system was applied in solar-driven treatment, solar/TiO₂-SnS₂/H₂O₂, for the purification of water contaminated with diclofenac (DCF). The effectiveness of studied reactivation methods for retaining TiO₂-SnS₂ activity in consecutive cycles was evaluated on basis of DCF removal and conversion, and TOC removal and mineralization of organic content. Besides these water quality parameters, biodegradability changes in DCF aqueous solution treated by solar/TiO₂-SnS₂/H₂O₂ process using simply reused (air-dried) and thermally and chemically reactivated composite photocatalyst through six consecutive cycles were monitored. It was established that both thermal and chemical reactivation retain TiO₂-SnS₂ activity in the second cycle of its reuse. However, both treatments caused the alteration in the TiO₂-SnS₂ morphology due to the partial transformation of visible-active SnS₂ into non-active SnO₂. Such alteration, repeated through consecutive reactivation and reuse, was reflected through gradual activity loss of TiO₂-SnS₂ composite in applied solar-driven water treatment.

Polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) were labeled potential persistent organic pollutants by the Stockholm Convention and have structures and toxicities similar to those of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), which has caused considerable concern. This article reviews the current available literature on the status, sources, formation pathways, and analysis of PBDD/Fs. PBDD/Fs are widely generated in industrial thermal processes, such as those for brominated flame retardant (BFR) products, e-waste dismantling, metal smelting processes, and waste incineration. PBDD/Fs can form via the following routes: precursor formation, de novo formation, biosynthesis, and natural formation. The levels of PBDD/Fs in the environment and in organisms and humans have increased due to extensive consumption and the increasing inventory of BFRs; thus, the risk of human exposure to PBDD/Fs is expected to be high.

Airborne pollutant characteristics, potential sources, and variation trends of cause are investigated based on the hourly air concentrations of gaseous pollutants and particulate matter from 2013 to 2016 in Lanzhou. The mean concentration of SO₂, NO₂, CO, 8-hO₃, PM₂.₅, and PM₁₀ was 25.2 ± 16.0 μg m⁻³, 46.5 ± 21.1 μg m⁻³, 1.3 ± 0.7 mg m⁻³, 77.8 ± 45.5 μg m⁻³, 58.7 ± 32.9 μg m⁻³, and 131.1 ± 86.2 μg m⁻³, respectively. The concentrations of SO₂, PM₁₀, and PM₂.₅ present decreasing trends while NO₂, CO, and O₃ present increasing trends. PM is the most frequent major pollutants with much higher value than standard limit. However, NO₂ pollution had obvious trends to reach the limit and was more serious in Lanzhou compared with other Chinese cities. Relationship between air pollutants and meteorological parameters suggested that lower primary pollutants were associated with higher wind speed from north and west. Modeled back trajectory demonstrated that the transport of air masses from the Hexi Corridor and Inner Mongolia was responsible for the high concentrations of the air pollutants in wintertime, and high PM₁₀ level in springtime was related to long-range transport of dust from desert areas of the Sinkiang and the Central Asia. Effects of local pollutant emissions and meteorological condition were preliminary analyzed. Improvement of air quality might be related to the decreasing of pollutant emissions due to strict emissions controls, and the contribution of meteorological condition was not explicit and should be further investigated.

The lack of management in small-scale mining operations has the potential for negative repercussions, e.g., mine collapses, compared with well-regulated large-scale mines. Here, we used an in vitro model to investigate heavy metal soil pollution characteristics and their attendant health risks in an abandoned, small-scale lead (Pb) and zinc (Zn) mine located in southwestern China that had suffered from collapse. Our results showed the following: (1) Even the mine had been closed for many years, the soil was still heavily polluted by Pb, cadmium (Cd), and Zn, and there is a risk of secondary pollution. Pb, Zn, and Cd concentrations in the mining areas were all approximately 22–42 times higher than the background soil levels of Guangxi Province. (2) Cd had the largest bioaccessibility, and mining areas tend to have soils containing more bioaccessible metals (78 ± 14%, 27 ± 4%, and 38 ± 12% for Cd, Pb, and Zn in gastric phase and 40 ± 12%, 10 ± 5%, and 19 ± 8% in intestinal phase correspondingly). (3) Results of a stepwise, multiple regression analysis revealed that the total soil content of the three metals (Pb, Zn, and Cd), TOC (total organic carbon), soil composition, and Mn content were the main impact factors for the Pb, Cd, and Zn soil bioaccessibility in study area (R² = 0.37~0.93). (4) A health risk assessment based on Pb, Cd, and Zn bioaccessibility indicated that the health risk for people in mine area is not high (HI is 1.07 at most and CR 2.40E−6 at most for children).

Di(isononyl)cyclohexane-1,2-dicarboxylate (DINCH) is a plasticizer used in polyvinyl chloride (PVC) products, such as toys and food packaging. Because the use of DINCH is on the rise, the risk of human exposure to this chemical may likewise increase. Discovering markers for assessing human chemical exposure is difficult because the metabolism of chemicals within humans is complex. In this study, two mass spectrometry (MS)-based metabolite profiling data processing methods, the mass defect filter (MDF) method and the signal mining algorithm with isotope tracing (SMAIT) method, were used for DINCH metabolite discovery, and 110 and 18 potential DINCH metabolite signal candidates were discovered, respectively, from in vitro DINCH incubation samples. Of these, the 21 signals were validated as tentative exposure marker signals in a rat model. Interestingly, the two methods generated rather different sets of DINCH exposure markers. Five of the 21 tentative exposure marker signals were verified as the probable DINCH structure-related metabolite signals based on their MS/MS product ion profiles. These five signals were detected in at least one human urine sample. Of the five probable DINCH structure-related metabolite signals, two novel signals might be suitable exposure markers that should be further investigated for their application in human DINCH exposure assessments. These observations indicate that the MDF and SMAIT methods may be used to discover a relatively different set of potential DINCH exposure markers.

Sonicated activated carbon (SAC) was developed and used to remove ibuprofen and ketoprofen from aqueous media by adsorption. A standard activated carbon sample (AC) was used as comparison. Both adsorbents were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), N₂ adsorption isotherms (Brunauer, Emmett, and Teller (BET)), helium gas pycnometry, and scanning electron microscopy (SEM). In the adsorption study, kinetics, equilibrium, and thermodynamics were evaluated. SAC presented better characteristics than AC. Pseudo-second-order model was adequate to predict the kinetic curves. The isotherm data obeyed the Sips model. Thermodynamic results revealed a spontaneous and endothermic process, where physisorption was involved. The maximum adsorption capacities of SAC were 134.5 and 89.2 mg g⁻¹ for ibuprofen and ketoprofen, respectively. For AC, the maximum adsorption capacities were 115.1 and 79.1 mg g⁻¹ for ibuprofen and ketoprofen, respectively. The sonication technique presented great potential to improve the AC characteristics, generating a promising material (SAC) for ibuprofen and ketoprofen adsorption.

The study mainly focuses on surface properties to investigate the deactivation factors of Pt/MnO ₓ -CeO₂ by H₂ temperature-programmed reduction, CO chemical adsorption, NO ₓ -temperature-programmed desorption (TPD), O₂-TPD, NO temperature-programmed oxidation, SEM, TEM, in situ diffuse reflectance infrared Fourier transform spectra, Raman, and thermogravimetric methods. The results show that there are three main factors to lead to hydrothermal deactivation of the catalyst: redox property, oxygen vacancy, and surface nitrates. The loss of oxygen vacancies decreases the generation and desorption of active oxygen and that of surface nitrates weakens the production of NO₂ and surface peroxides (-O₂⁻). These factors greatly result in the damage of the C-NO₂-O₂ cooperative reaction.