Natural organic matter reacted with chlorine used for disinfection, and finally, trihalomethanes (THMs) are formatted. The main purpose of this study was to determine four THM concentrations and human health cancer risk and non-cancer risk assessment from exposure through oral ingestion, dermal contact, and inhalation for males and females in Abadan. Two sampling sites were selected, and five samples before and after treatment by two different water treatment systems (RO and ion exchange) were collected every week. Results showed that total THM concentrations before and after treatment by RO were 98.1 and 8.88 μg/L, and ion exchange ranged between 101.9 and 14.96 μg/L, respectively, that before treatment was upper than the maximum of 80 mg/L recommended by USEPA. Inhalation was the primary route of exposure by around 80–90% of cancer risk. Total cancer risk was higher than the USEPA acceptable limit of 10?6 via three exposure routes. Oral route has the higher hazard index values than dermal ways.
The environmental assessment of potential effects of contaminated harbor sediments stabilized with hydraulic binders and the determination of remediation endpoints require the determination of pollutants leaching potentials. Moreover, little information about the speciation and mobility of inorganic contaminants in these specific solid matrices is available in the literature. The objective of this paper is to investigate the relationship between mineralogy and leachability of contaminants (copper, lead, and zinc) present in a French harbor sediment stabilized with quicklime and Portland cement. Batch equilibrium leaching tests at various pH, chemical analysis of leachates, and mineralogical studies (X-ray diffraction, scanning electron microscopy–energy dispersive spectroscopy, and diffuse reflectance infrared Fourier transform) have been combined in the present investigation. The acid neutralization capacity of the stabilized matrix studied is first controlled by the dissolution of portlandite (pH?~12), followed by the dissolution of C–S–H (pH?~11) and the dissolution of ettringite (pH?~10). Finally, a very high buffering capacity of this stabilized sediment is observed for pH values around 6. This equilibrium is mainly controlled by the dissolution of iron sulfides and carbonate minerals. Consequently, the mobilization of inorganic contaminants as a function of pH remains very low (<0.1 wt%) for pH values above 6 and significantly increases for pH below these values. This research confirms the importance of a combined methodology for the intrinsic characterization of potential mobilization of contaminants in a stabilized sediment and for a better understanding of geochemical processes that affect contaminant fate, transformation, and transport in the subsurface environment. 相似文献
One of the most pressing issues in studying the impacts of sea level rise (SLR) triggered by climate change is understanding the development of the hazard of permanent coastal flooding. The issue persists because available approaches are based on the mapping of the inundated area where they explore the coastal flooding development across terrain elevations, that is—horizontally. In addition, they overlook the existing structures along or in the vicinity of the coastline, which have inherent hydraulic properties that may affect the development of such flooding. The purpose of this study is to develop a novel approach for assessing the development of permanent coastal flooding due to SLR at cross sections along the coastline, that is—vertically, in full consideration of underlying hydraulic properties of the existing coastline. An approach was developed using analogy of existing coastline to a contiguous weir. This approach was named crestline approach and was developed as a four step GIS-based approach that could be applied at any coastal zone. An example application on one of the top ranked cities in the world prone to the SLR threat has been provided to illustrate exactly how to apply the crestline approach. The novelty of this approach lies in its ability to accurately identify the specific locations where coastal flooding will initiate, in full consideration of existing natural/manmade coastal structures. This study is significant for the opportunities it provides to analysts and decision makers to better understand the development of permanent coastal flooding. 相似文献
In the last three decades, the industrial and human activities in the coastal area of Saudi Arabia have increased dramatically and resulted in the continuous invasion of different types of pollutants including heavy metals. Seven sediment cores were collected from three major industrialized areas; Jeddah, Rabigh and Yanbu, along the coast of Saudi Arabia to determine the spatial and temporal distribution of metals and to assess the magnitude of pollution and their potential biological effects. Sediments were analyzed for texture, calcium carbonate contents, organic matter and metals (Al, Fe, Mn, Cd, Cr, Cu, Ni, Pb and Zn). Some metals like, Cr, Mn, Ni and Zn, were enriched in the upper 15 cm of core samples (recent deposition of sediments). Cadmium concentrations showed high fluctuations with depth and reverse pattern to that for Al, Fe and Mn which indicated land based sources of this element to the studied areas. Elevated concentrations of lead were recorded in the bottom layers of cores in Jeddah that indicated the most dramatic increase in usage of gasoline in early 1970s. The calculated contamination factors (CF's) were found in the following sequences: Cd > Pb > Ni > Cu > Zn > Cr > Mn for all studied areas. Results of Pollution Load Index (PLI) revealed that Jeddah is the most polluted area, followed by Rabigh while Yanbu is the least contaminated area. Except for Ni, the concentrations of most metals in the majority of sediment samples were believed to be safe for living organisms. As no data were available on the concentration of metals in core sediments in the coastal area of Saudi Arabia, the results of this study would serve as a baseline against which future anthropogenic effects can be assessed. 相似文献
Abstract Potato tubers were applied with radiolabelled lindane (U‐14C γ‐ 1,2,3,4,5,6 hexachlorocyclohexane) at three dose levels 30, 150, and 300 ppm and stored for 30, 60 and 90 days at room temperature. The data revealed that lindane penetrated into the pulp tissues through the epidermal layer. The amounts recovered in the peel were found to increase with a greater storage period up to 60 days followed by a drop at 90 days. On the other hand, there was a slight increase in radioactivity in the pulp tissue from 30 to 60 days followed by significant increase after 90 days. The incorporation of the compound in the tubers was dose independent. Methanol extraction showed binding of about 8.1% and 5.8% ofthe applied dose in peel and pulp tissues, respectively. The insecticide was found to be bioavailable when rats health hazard. It is therefore, desirable to demonstrate that the quantity of the terminal residues may be safe for the consumer. In the present investigation an attempt was made to determine the fate and bioavailability of lindane when applied to stored potato tubers. 相似文献
Abstract3H‐Trifluralin was synthesized by condensation of 3H‐4‐chloro‐3,5‐dinitro‐α, α, α‐trifluorotoluene with di‐n‐propylamine. After incubation of trifluralin with Aspergillus carneus, Fusarium oxysporum and Trichoderma viride for 10 days, a small percentage (less than 10%) of unchanged herbicide was recovered in the extractable fraction. This indicates a fairly rapid degradation of the herbicide by the fungal species. Other than trifluralin, the culture medium contained at least five labelled products: 2, 6‐dinitro‐N‐n‐propyl‐α, α, α‐tri‐fluoro‐p‐toluidine; 2, 6‐dinitro‐α, α, α‐trifluoro‐p‐toluidine; 2‐amino‐6‐nitro‐α, α,‐trifluoro‐p‐toluidine, 2, 6‐dinitro‐4‐trifluoromethyl phenol and a major polar product which constituted more than 50% of the total extractable transformation products. A pathway, which similates that of aerobic degradation of the herbicide in soil, is suggested for the microbiological degradation of trifluralin. 相似文献
Natural bituminous coal was used as a precursor in the synthesis of different modified products. The modification of coal was performed by treating it with nitric acid (N-coal), coating its surface by zinc oxide nanoparticles (Z-coal), and converting it into porous graphite (PG). The effect of modification processes on the structures, morphologies, and optical properties was followed by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectrum (FT-IR), and UV/VIS spectrophotometer analysis. The surface of N-coal grains becomes smoother than the surface of raw coal grains due to the removal of the associated impurities and the formation of nitrogen function groups. For Z-coal, the whole surface of coal grains appears to be completely covered by agglomerated ZnO nanoparticles of massive density and irregular shapes. The average crystallite size of the formed ZnO is ~22.2 nm and density of dislocations is 2.029 × 10?3 dislocation/nm2. Also, the removal of safranin-T dye by natural bituminous coal and its modified forms was investigated as a function of contact time, adsorbent mass, initial dye concentration, and pH value. At pH 8, the PG showed higher efficiency (96%) than Z-coal (93.5%), N-coal (74.5%), and natural coal (62%) after 2 h for 0.1 g on 100 mg/L dye. The obtained results are well fitted by pseudo-second-order kinetic than by intraparticle diffusion and Elovich kinetic models for the adsorption by N-coal, Z-coal, and PG, whereas the adsorption by raw coal is well fitted with both pseudo-second-order and Elovich kinetic models. The Langmuir isotherm model fits well the equilibrium adsorption isotherm of safranin by raw coal and its modified forms. The values of maximum adsorption capacity were calculated for raw coal, N-coal, Z-coal, and PG to be 21.3, 27.4, 32.46, and 33.67 mg/g, respectively. A monolayer model with one energy and a monolayer model with two energies as advanced equilibrium models were investigated for more physical interpretation of the adsorption process. The calculated parameters (number of adsorbed molecules per site and number of receptor sites per unit mass) reflected the role of modification processes in the adsorption behavior of safranin.
Abstract The effect of methomyl and cypermethrin insecticides on the B6‐dependent kynurenine hydrolase(KH) and kynurenine aminotransferase (KATE) was studied. These insecticides induced pronounced inhibition on the (KH) and (KATE) enzymes after single dose treatment. Repeated doses of methomyl induced inhibition on the (KH) and (KATE) activities, whereas repeated treatment with cypermethrin had no effect on the activities of these enzymes. In vitro methomyl inhibited (KH) and (KATE) enzymes at 10 M up to 10‐3 M, through a competitive mechanism. Methomyl and cypermethrin are capable of causing alterations in the kynurenine metabolizing enzymes of mouse liver. 相似文献