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The interaction between water environment and social economy at a basin scale is complex and challenging to quantify. To address this issue, this study proposes an integrated framework that builds parametric connections among water, contaminants, administrative regions, and social activities. The framework, known as the water environmental carrying capacity (WECC) optimization framework, effectively captures the intricacy of the interaction and integrates socio-economic parameter structure relationships, a water environmental model, a WECC optimization model, and a sensitivity analysis of regulatory parameters. Applied to the Anhui-Huaihe Basin in mid-eastern China, the framework considers nine administrative regions and three economic factors: industry, agriculture, and GDP per capita (pGDP). Results show that the current water environmental carrying capacity of the watershed is insufficient to meet socio-economic development requirements. After optimization, the WECC for industry, agriculture, and pGDP in the region increased by 22.40%, 26.59%, and 15.08% respectively. Overall COD and NH4-N discharge decreased by 13.6% and 14.7% respectively, effectively reducing pollution loads in rivers and enhancing sustainable development potential. At the regional scale, optimization for industry, agriculture, and pGDP exhibited different characteristics, but all aimed to improve efficiency by reducing the K value (pollution discharge/output value ratio). Regions with industrial treatment rates (αwt) below 0.8 should prioritize increasing treatment rates, while those above 0.8 should consider industrial upgrading for enhanced efficiency. For agriculture, important sensitive parameters for farming and livestock breeding are the proportion of high standard farmland (αs) and the scale breeding ratio (αb), which should be increased to above 0.15 and 0.83 respectively for all regions to achieve agricultural optimization. For pGDP optimization, the focus is on improving living environments and reducing pollution discharge, with crucial measures including collecting and treating rural domestic sewage, where the rural toilet improvement rate (αt) in each region should be increased to 0.78 or above. The results emphasize the need for both interregional allocation and intraregional planning to achieve comprehensive basin optimization and a harmonious balance between regional development and water environment.
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Conservación de los Recursos Naturales , Agua , Contaminación Ambiental , Ríos/química , Agricultura , ChinaRESUMEN
Graphitic carbon nitride (CN), as a non-metal material, has emerged as a promising photocatalyst to address environmental issues with the favorable band gap and chemical stability. The porous oxygen-doped CN nanosheets (CNO) were synthesized by an ecofriendly and efficient self-assembled approach using a sole urea as the precursor. The CNO photocatalysts were derived from the hydrogen-bonded cyanuric acid-urea supramolecular complex, which were obtained by pretreatment of urea at high temperature and pressure. The homogeneous supramolecular assembly was advantageous to the formation of uniform porous and oxygen-doped CN nanosheets. The formation process of the supramolecular intermediate and the CNO nanosheets were investigated. Moreover, doping amount of O in CNO could be controlled by the time of the high-pressure thermal polymerization of urea. The characterization results shown that the O atoms were successfully doped into the framework of CN by substitution the N atoms to form the C-O structures. The obtained CNO photocatalysts demonstrated the excellent visible-light photocatalytic performances for sulfamerazine (SMR) degradation, which was ascribed to synergistic interaction of porous structure and O doping. The degradation intermediates of SMR were identified and the degradation pathway were also proposed. Furthermore, density functional theory (DFT) calculations proved that O doping changed the electronic structure of CN, resulting in more easier to activate O2. This work provides a novel perceptive for the development of high-performance nonmetal photocatalysts by using the homogeneous supramolecular assembly, which exhibits great potential in the environmental treatment.
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Contaminantes Ambientales , Oxígeno , Antibacterianos , Catálisis , Grafito , Luz , Compuestos de Nitrógeno , Oxígeno/química , UreaRESUMEN
The combination of adsorption-photocatalysis and advanced oxidation processes (AOP) based on sulfate (SO4â¢-) for the treatment of organic pollution has the advantages of a high degradation rate, affordability, and an absence of secondary pollution. This study combined amphiphilic super-crosslinked porous cyclodextrin resin (PBCD-B-D), bismuth oxybromide (BiOBr), a composite material with dual functions of adsorption and photocatalysis, and AOP based on SO4â¢- for the treatment of Acid Orange 7 (AO7) in water. The combination of BiOBr/PBCD-B-D (BOP-24) with peroxymonosulfate (PMS) showed an optimal adsorption-photocatalytic effect. Compared to the 24% PBCD-B-D (BOP-24)/visible light system, the degradation efficiency of BOP-24/PMS system for AO7 is increased from 64.1% to 99.2% within shorter time (â¼60 min). Moreover, the BOP-24/PMS system showed a wide range of pH application (pH = 3-11). The addition of Cl-, SO42-, and NO3- promoted the photodegradation of AO7, whereas the addition of CO32- did not. The free radical capture experiments of the BOP-24/PMS AO7 degradation system showed that â¢O2-, h+, â¢OH, and SO4â¢- are reactive species. The proposed BOP-24 system used adsorption and a unique cavity structure to enrich AO7 near the active site, thereby reducing the path for PMS activation. PMS also acted as an electron (e-) acceptor to promote the transfer of part of e- to PMS, thereby further improving the efficiency of carrier separation. The proposed system is an effective method to improve the degradation of pollutants and broadens the range of application of SO4â¢--based AOP technology.
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Ciclodextrinas , Contaminantes Ambientales , Contaminantes Químicos del Agua , Bismuto , Celulosa , Luz , Oxidación-Reducción , Peróxidos , Agua , Contaminantes Químicos del Agua/análisisRESUMEN
Taihu Lake is the most important drinking water source of the major cities in the Yangtze River Delta. The pollution of endocrine disruptors (EDCs)in Taihu Lake has been increasing recently, the accurate determination is an important guide for predicting its health risks and developing appropriate controls. Monitoring organic pollutants in water using the diffusive gradient in thin film technique (DGT) has attracted much attention due to more accuracy and convenience than the grab sampling methods. In this study, a novel cyclodextrin polymer (CDP) synthesized by the simple and green method in water was taken as an adsorbent for the binding gel. Four endocrine-disrupting chemicals (EDCs), bisphenol A (BPA), 17α-ethinylestradiol (EE2), 17ß-estradiol (E2), and estriol (E3), were taken as models to determine the diffusion coefficients (4.68 × 10-6, 3.38 × 10-6, 3.34 × 10-6 and 4.31 × 10-6 cm2/s) and to test the performance of DGT, such as adsorption capacity and deployment time (1-5 day). The assembled CDP-DGT was adopted to determine four EDCs in a simulated water environment (3-9 of pH, 0.001-0.5 M of ionic strength (IS), and dissolved organic matter (DOM) of 0-20 mg/L). The ability of CDP-DGT sampling was verified in the Jiuxiang River and was carried out for a large-scale field application of in situ sampling EDCs in Taihu Lake basin. The results show that the total EDCs concentration range and the estradiol equivalent concentrations (EEQ) in Taihu Lake and its main rivers are 2.78 ng/L to 11.08 ng/L and 2.62 ng/L to 10.91 ng/L, respectively. The risk quotients (RQs) of all sampling sites in the region were greater than 1, indicating that EDCs pose a serious threat to aquatic organisms in the area. Therefore, the monitoring of EDCs in the Taihu Lake basin should be further strengthened.
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Disruptores Endocrinos , Contaminantes Químicos del Agua , Celulosa , China , Ciclodextrinas , Disruptores Endocrinos/análisis , Monitoreo del Ambiente/métodos , Estradiol , Geles , Lagos/química , Medición de Riesgo , Ríos/química , Agua , Contaminantes Químicos del Agua/análisisRESUMEN
The fractions transformation and dissipation mechanism of Dechlorane Plus (DP) in the rhizosphere of soil-plant system were investigated and characterized by a 150-day experiment using a rhizobox system. The depuration, accumulation, and translocation of DP in rice plants were observed. The contributions of plant uptake, microbial degradation, and bound-residue formation to DP dissipation under the rhizosphere effect were modeled and quantified. The gradients of DP concentrations correlated well with microbial biomass in the rhizosphere (R2 = 0.898). The rhizosphere facilitated the bioavailability of DP (excitation) and modified the bound-residue formation of DP (aging). DP concentrations in roots were positively correlated with the labile fraction of DP in soil (R2 = 0.852-0.961). There were spatiotemporal variations in the DP fractions. Dissolved and soil organic carbon were important influences on fraction transformation. Contributions to total DP dissipation were in the following ranges: microbial degradation (8.33-54.14%), bound-residue formation (3.64-16.43%), and plant uptake (0.54-3.85%). With all of these processes operating, the half-life of DP in the rhizosphere was 105 days. The stereoselectivity of DP isomers in both rice and DP fractions in soil were observed, suggesting a link between stereoselective bioaccumulation of DP in terrestrial organisms and dissipation pathways in soil.
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Hidrocarburos Clorados , Contaminantes del Suelo , Carbono , Hidrocarburos Clorados/análisis , Raíces de Plantas/química , Compuestos Policíclicos , Rizosfera , Suelo , Microbiología del Suelo , Contaminantes del Suelo/análisisRESUMEN
Adsorption is one of the most preferred techniques in the advanced treatment of dyeing wastewater. Magnetic porous materials with good adsorption performance, excellent reusability, and a green synthesis route are highly desirable adsorbents in commerce. In this study, we synthesized a magnetic ß-cyclodextrin polymer (MNP-CM-CDP) containing many macro- and ultramicropores in aqueous phase. CO2 adsorption-desorption isotherms and a dye adsorption method provided Langmuir specific surface areas for the MNP-CM-CDP of 114.4â¯m2â¯g-1 and 153â¯m2â¯g-1, respectively. Model pollutants (BPA, MB, BO2, RhB, Cr(III), Pb(II), Zn(II), and Cu(II)) were rapidly and efficiently removed from the aqueous solution by the MNP-CM-CDP. In addition, the polymer could be easily separated from the solution under an external magnetic field. The adsorption of the contaminants was dependent on pH, while the effects of ionic strength and humic acid were slight in the concentration range studied. The polymer could be easily regenerated at room temperature and retained good adsorption performance. Moreover, the MNP-CM-CDP showed good feasibility for the removal of pollutants from actual dyeing wastewater samples.
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Contaminantes Ambientales , Metales Pesados , Aguas Residuales , Contaminantes Químicos del Agua , Adsorción , Celulosa , Ciclodextrinas , Fenómenos Magnéticos , PolímerosRESUMEN
A 3-step sequential extraction method was developed to characterize the "labile," "stable-adsorbed," and "bound-residue" fractions of Dechlorane Plus (DP) in aging soils. Afterward, the proposed method was used to observe the transformation of DP fractions during aging. Slight decrease of total DP concentrations suggested there was a rather limited degradation, with only 4.2-8.2% of initial DP having degraded after 260 days. The labile fraction, which indicated the bioavailability of DP, decreased from 25.5% to 8.2%. The bound-residue fraction, usually regarded as a route for detoxification, increased from 0.1% to 18.5%. Model simulations were then developed to investigate the transformation, indicating that transformation rates were inconstant and distinguishable over time. Half-lives of DP were estimated to range from 1325 to 2948 days, indicating its environmental persistence in aging soils. Through Sobol Global Sensitivity Analysis (SGSA), degradation was evaluated to be the most sensitive factor of effecting the DP transformation in aging soils. Furthermore, the fsyn values increased from 0.26 to 0.37 in the labile fraction and decreased from 0.25 to 0.18 in the bound-residue fraction. The observed stereoselectivity difference might be the cause of the stereoselective accumulation of DP in terrestrial organisms.
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Contaminantes Ambientales , Retardadores de Llama , Hidrocarburos Clorados , Compuestos Policíclicos , Monitoreo del Ambiente , SueloRESUMEN
Herein we investigated the multi-phase distribution and estrogenic effects of endocrine disrupting chemicals (EDCs) in suspended particulate matter (SPM), colloids, and soluble phases from the Shaying River to assess the composition of estrogenic compounds and associated estrogenic risk. The yeast two hybrid (YES) method, cross-flow ultrafiltration (CFUF), and LC-MS/MS were employed. Risk quotient (RQ) values ranged from 0.72 to 3.88, revealing that the Shaying River posed high estrogenic risk to aquatic organisms. The contribution ratios of the target EDCs to the EEQYES ranged from 62.7% to 92.5%, indicating that these chemicals were major contributors of estrogenic effects in the Shaying River. Further, 54.0-77.8% of the detected EDCs were distributed in the soluble phase, 15.1-31.7% were bound to colloidal substances, and 3.90-19.4% EDCs were associated with SPM. Significant correlation between total EDC abundance and COD contents was detected, and the concentrations of endogenous estrogens (E1, E2, and E3) were positively correlated with total nitrogen (TN) and total phosphorus (TP). In addition, the in-situ SPM-soluble (Kpoc) and colloid-soluble partition (Kcoc) coefficients were calculated. The log Kpoc values of target compounds varied from 4.10 to 5.19, while log Kcoc values ranged from 4.25 to 5.56. Their Kcoc values were larger than the Kpoc values, indicating that organic colloids were the most important carriers of EDCs in the aquatic environment.
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Disruptores Endocrinos/análisis , Estrógenos/análisis , Ríos/química , Contaminantes Químicos del Agua/análisis , Organismos Acuáticos , China , Coloides/química , Disruptores Endocrinos/química , Monitoreo del Ambiente , Estrógenos/química , Material Particulado/química , Medición de Riesgo , Contaminantes Químicos del Agua/químicaRESUMEN
A novel metal-free oxygen-doped graphitic carbon nitride (O-g-C3N4) was synthesized by the pre-treatment of bulk graphitic carbon nitride (g-C3N4) with hydrogen peroxide (H2O2), and combined with high-temperature calcination treatment. The obtained 2-O-g-C3N4 catalyst exhibits high activity in visible light photocatalytic degradation of bisphenol A (BPA) with a mineralization rate as high as 62.3%. According to the characterization results of X-ray diffraction, transmission electron microscopy, UV-visible spectroscopy, Brunauer-Emmett-Teller and photoluminescence spectroscopy analyses, the markedly higher visible-light-driven oxidation activity of 2-O-g-C3N4 is attributed to the larger specific surface area, wider range of light responses and low charge recombination rate. Moreover, the trapping experiment shows that superoxide radicals (â¢O2 -) are the dominant active species in the BPA decomposition process over 2-O-g-C3N4. This study presents a simple and environment-friendly method to synthesise oxygen-doped graphitic carbon nitride.
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Compuestos de Bencidrilo/química , Luz , Nitrilos/química , Oxígeno/química , Fenoles/química , Catálisis , Peróxido de Hidrógeno , Microscopía Electrónica de Transmisión , Contaminantes Químicos del Agua/química , Purificación del Agua , Difracción de Rayos XRESUMEN
Studies have shown the main fate of the flame retardant tetrabromobisphenol A (TBBPA) in soils is the formation of bound residues, and mechanisms on it are less-understood. This study investigated the effect of birnessite (δ-MnO2), a naturally occurring oxidant in soils, on the formation of bound residues. (14)C-labeled TBBPA was used to investigate the pH dependency of TBBPA bound-residue formation to two soil humic acids (HAs), Elliott soil HA and Steinkreuz soil HA, in the presence of δ-MnO2. The binding of TBBPA and its transformation products to both HAs was markedly increased (3- to 17-fold) at all pH values in the presence of δ-MnO2. More bound residues were formed with the more aromatic Elliott soil HA than with Steinkreuz soil HA. Gel-permeation chromatography revealed a uniform distribution of the bound residues within Steinkreuz soil HA and a nonuniform distribution within Elliott soil HA. (13)C NMR spectroscopy of (13)C-TBBPA residues bound to (13)C-depleted HA suggested that in the presence of δ-MnO2, binding occurred via ester and ether and other types of covalent bonds besides HA sequestration. The insights gained in this study contribute to an understanding of the formation of TBBPA bound residues facilitated by δ-MnO2.
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Sustancias Húmicas , Suelo/química , Ésteres , Retardadores de Llama , Contaminantes del SueloRESUMEN
The ecological restoration of rare earth mines and the management of rare earth tailings have consistently posed global challenges, constraining the development of the rare earth industry. In this study, Zeolite A is efficiently prepared from the tailings of an ion-type rare earth mine in the southern Jiangxi Province of China. The resulting Zeolite A boasts exceptional qualities, including high crystallinity, a substantial specific surface area, and robust thermal stability. The optimum conditions for Zeolite synthesis are experimental determination and the adsorption properties of Zeolite A for typical pollutants (Cd2+, Cu2+, NH4+, PO43- and F-) in rare earth mines. The synthesised Zeolite A material is found to have strong adsorption properties. The adsorption mechanism is mainly cation exchange, and the priority of adsorption of pollutants is Cu2+> Cd2+ > NH4+ > PO43- > F-. Notably, the sodium Zeolite A material synthesized at room temperature can be effectively recycled multiple times. In summary, we propose a method to synthesise low cost and high adsorption zeolites using rare earth tailings. This will facilitate the reduction of rare earth tailings and the rehabilitation of rare earth mines. Our method has great potential as a rehabilitation technology for rare earth mines.
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Disinfection is vital in ensuring water safety. However, the traditional chlorine disinfection process is prone to producing toxic and harmful disinfection by-products (DBPs). The combination of quaternary ammonium polymer and the chlorine disinfection process can solve this shortcoming. Currently, research on the control of DBPs through the combined process is not systematic and the control effect between reducing the dosage of disinfectants and DBPs remains to be studied. Quaternized cyclodextrin polymers have attracted increasing attention due to their excellent adsorption and antibacterial properties, but their synergistic effect with chlorine disinfection is still unclear. In this study, a magnetic quaternized cyclodextrin polymer (MQCDP) is synthesized in an ionic liquid green system, and a combined process of MQCDP treatment and chlorine disinfection is established. The disinfection performance of the combined process on the actual water body along with its reducing effect on the amount of chlorine disinfectant as well as the trihalomethanes (THMs) and haloacetic acids (HAAs) DBPs are explored. MQCDP has a porous structure with a specific surface area of 825 m2 g-1 and is easily magnetically separated. MQCDP can remove most of the natural organic matter (UV254 absorbance decreased by 97 %) in the water at the dosage of 1 g L-1 and kill bacteria with a sterilization rate of 85 %. Compared with disinfection using chlorine alone, the combined process has higher disinfection efficiency and significantly reduces the amount of disinfectant used. A concentration of 5 mg/L of NaClO was needed to meet the standard by chlorine disinfectant alone, while only 2 mg/L of NaClO can meet the standard for the combined process, indicating 60 % of the chlorine demand was reduced. More importantly, the combined process can significantly reduce the generation potential of DBPs. When 10 mg/L of NaClO is added, the THMs and HAAs generated by the combined process decreased by 65 % and 34 %, respectively, compared with the levels produced by single chlorine disinfection. The combined process can reduce the dosage of chlorine disinfectant and MQCDP can adsorb humic acid DBP precursors in raw water, thus lowering the generation of DBPs during disinfection. In summary, MQCDP has excellent separation and antibacterial ability, and its synergistic effects combined with the chlorine disinfection process are of great significance for controlling the amount of disinfectant and the formation potential of DBPs, which has potential applications in actual water treatment.
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Celulosa , Ciclodextrinas , Desinfectantes , Contaminantes Químicos del Agua , Purificación del Agua , Desinfección , Cloro/química , Desinfectantes/química , Cloruros/química , Halogenación , Trihalometanos/química , Antibacterianos/farmacología , Fenómenos Magnéticos , Contaminantes Químicos del Agua/análisisRESUMEN
In this paper, the two-dimensional (2D) layered CoAl LDH (CoAl) was coupled with Bi2MoO6 (BMO) nanoplate and used for tetracycline (TC) degradation. Based on the results of UV-visible diffuse reflectance spectrum (UV-vis DRS), Motty-Schottky curves, and in situ X-ray photoelectron spectroscopy (XPS), a novel 2D/2D Bi2MoO6/CoAl LDH S-scheme heterojunction photocatalyst was built. The photodegradation rate constant of TC by the optimized sample BMO/CoAl30 was 3.637 × 10-2 min-1, which was 1.26 times and 4.01 times higher than that of Bi2MoO6 and CoAl LDH, respectively. The favorable photocatalytic performance of the heterojunction was attributed to the increased interfacial contact area of the 2D/2D structure. Besides, the transfer of photogenerated electrons from Bi2MoO6 to CoAl LDH under the effect of the built-in electric field (BIEF) reduced the recombination of photogenerated carriers and further improved the photocatalytic performance. The reactive species of h+, ·O2-, and 1O2 exhibited critical roles to degrade TC molecules by reactive radicals capture experiments and electron spin resonance (ESR) tests. The intermediate products of TC degradation and toxicity of intermediates were analyzed by liquid chromatography-mass spectrometer (LC-MS) and Toxicity Estimation Software Tool (T.E.S.T). Additionally, the BMO/CoAl composite photocatalysts showed high stability and environmental tolerance during the testing of cycles and environmental impacts with various water sources, organic contaminants, initial pH, and inorganic ions. This work provides a new protocol for designing and constructing novel 2D/2D S-scheme heterojunction photocatalysts for wastewater treatment.
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Compuestos Heterocíclicos , Tetraciclina , Antibacterianos , Bismuto , Cromatografía Liquida , Carbón MineralRESUMEN
Nanoscale zerovalent iron (nZVI) has garnered significant attention as an efficient advanced oxidation activator, but its practical application is hindered by aggregation and oxidation. Coating nZVI with carbon can effectively addresses these issues. A simple and scalable production method for carbon-coated nZVI composite is highly desirable. The anti-oxidation and catalytic performance of carbon-coated nZVI composite merit in-depth research. In this study, a highly stable carbon-coated core-shell nZVI composite (Fe0@RF-C) was successfully prepared using a simple method combining phenolic resin embedding and carbothermal reduction. Fe0@RF-C was employed as a heterogeneous persulfate (PS) activator for degrading 2,4-dihydroxybenzophenone (BP-1), an emerging contaminant. Compared to commercial nZVI, Fe0@RF-C exhibited superior PS activation performance and oxidation resistance. Nearly 95% of BP-1 was removed within 10 min in the Fe0@RF-C/PS system. The carbon layer promotes the enrichment of BP-1 and accelerates its degradation through singlet oxygen oxidation and direct electron transfer processes. This study provides a straightforward approach for designing highly stable carbon-coated nZVI composite and elucidates the enhanced catalytic performance mechanism by carbon layers.
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With the intensification of human activities, the amount of phosphorus (P)-containing waste has increased. When such waste is not recycled, P is released into the environment, leading to environmental issues such as the eutrophication of water bodies. In this study, based on the material flow analysis method, a P Waste Flow analysis model (P-WFA) was developed to analyze the P flow in the waste system of Poyang Lake, the largest freshwater lake in China. To address the research gap in long-term P flow analysis at the watershed scale, this study quantified the P content in the waste system of the Poyang Lake Watershed from 1950 to 2020. The analysis revealed that from 1950 to 2020, the total P input into the waste system increased from 5.49 × 104 tons in 1950 to 2.28 × 105 tons in 2020. The breeding industry system was identified as the primary source, accounting for 25.19-41.59 % of the total waste system. Over the past 70 years, P loss to surface water from waste systems has been primarily facilitated by manure from the breeding industry, as well as drainage from crop farming systems (77.74 % in 2020). At the same time, the P recycling rate (PRR) of the waste system exhibited an initial increase followed by a decrease, increasing from 44.14 % to 47.75 % before dropping to 44.41 %. Population growth, urbanization, and changes in consumption levels in Jiangxi Province have led to changes in the dietary structure and fertilizer use, consequently affecting the P cycling pattern. This study presents a comprehensive P flow model for waste systems in the Poyang Lake Watershed. This model can be used as a reference to enhance P cycling and manage P loss in other large freshwater lakes.
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The seasonal occurrence and distribution of phosphite (HPO3(2-), P) in sedimentary interstitial water from Lake Taihu was monitored from 2011 to 2012 to better understand its possible link to P cycle in the eutrophic shallow lake. Phosphite concentrations ranged from < MDL to 14.32 ± 0.19 µg P/kg with a mean concentration of 1.58 ± 0.33 µg P/kg, which accounts for 5.51% total soluble P (TSP(s)) in surficial sediments (0-20 cm). Spatially, the concentrations of sedimentary phosphite in the lake's northern areas were relatively higher than those in the southern areas. Higher phosphite concentrations were always observed in seriously polluted sites. Generally, phosphite in the deeper layers (20-40 cm and 40-60 cm) showed minor fluctuations compared to that in the surficial sediments, which may be associated with the frequent exchange at the sediment-water interface. Phosphite concentrations in surficial or core sediments decreased as spring > autumn > summer > winter. Higher phosphite levels occurred in the areas with lower redox (Eh), higher P contents, and particularly when metal bonded with P to form Al-P(s) and Ca-P(s). Phosphite may be an important media in the P biogeochemical cycle in Lake Taihu and contribute to its internal P transportation.
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Lagos/análisis , Fosfitos/análisis , China , Monitoreo del Ambiente/métodos , Eutrofización , Sedimentos Geológicos/análisis , Sedimentos Geológicos/química , Lagos/química , Fósforo/análisis , Estaciones del Año , Contaminantes Químicos del Agua/análisisRESUMEN
The effects of decabromodiphenyl ether (BDE-209) on avoidance response, survival, growth, and reproduction of earthworms (Eisenia fetida) were investigated under laboratory conditions using natural and artificial soils as substrate. Results showed that no significant avoidance response was observed when earthworms were exposed to 0.1-1000 mg/kg of BDE-209 for 48 h. After 28-days exposure, no significant effects on survival and growth of adult earthworms was induced by 0.1-1000 mg/kg of BDE-209 indicating the Lowest Observed Effect Level (LOEL) of BDE-209 on their survival and body weight was more than 1000 mg/kg. Except for a significant decrease in the number of juveniles per hatched cocoon in artificial soils at 1000 mg/kg of BDE-209, no significant effects on reproductive parameters (e.g. cocoon production per earthworms, weight per cocoon and cocoon hatchability) were observed. These results suggest that adult earthworms have a strong tolerance for BDE-209 exposure in soils, but a potential toxicity does exist for earthworm embryos or juveniles.
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Éteres Difenilos Halogenados/toxicidad , Oligoquetos/efectos de los fármacos , Contaminantes del Suelo/toxicidad , Animales , Conducta Animal/efectos de los fármacos , Éteres Difenilos Halogenados/análisis , Oligoquetos/crecimiento & desarrollo , Oligoquetos/fisiología , Reproducción/efectos de los fármacos , Suelo/química , Contaminantes del Suelo/análisis , Análisis de SupervivenciaRESUMEN
Zero-valent iron (ZVI) is a promising technology for groundwater treatment, and its efficiency primarily depends on the electron transfer. However, there are still some problems such as low electron efficiency of ZVI particles and high yield of iron sludge that limits the performance, which warrant further investigation. In our study, a silicotungsten acidified ZVI composite (m-WZVI) was synthesized by ball milling to activate PS to degrade phenol. m-WZVI has a better performance on phenol degradation (with a removal rate of 91.82%) than ball mill ZVI(m-ZVI) with persulfate (PS) (with a removal rate of 59.37%). Compared with m-ZVI, the first-order kinetic constant (kobs) of m-WZVI/PS is 2-3 times higher than that of the others. Iron ion was gradually leached in m-WZVI/PS system, being only 2.11 mg/L after 30 min, having to avoid excessive consumption of active substances. The underlying mechanisms of m-WZVI for PS activation mainly include: 1) were elucidated through different characterizations analyses that accounted for silictungstic acid (STA) can be combined with ZVI, and a new electron donor (SiW124-) was obtained, which improved the transfer rate performance of electrons for activating PS; 2) singlet oxygen (1O2) is the main active substance for phenol degradation, but other radicals also played an important role. Therefore, m-WZVI has good prospects for improving the electron utilization of ZVI.
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Hierro , Contaminantes Químicos del Agua , Hierro/química , Oxidación-Reducción , Electrones , Contaminantes Químicos del Agua/química , FenolesRESUMEN
In modern geochemistry, phosphorus (P) is considered synonymous with phosphate (Pi) because Pi controls the growth of organisms as a limiting nutrient in many ecosystems. The researchers therefore realised that a complete P cycle is essential. Limited by thermodynamic barriers, P was long believed to be incapable of redox reactions, and the role of the redox cycle of reduced P in the global P cycling system was thus not ascertained. Nevertheless, the phosphite (Phi) form of P is widely present in various environments and participates in the global P redox cycle. Herein, global quantitative evidences of Phi are enumerated and the early origin and modern biotic/abiotic sources of Phi are elaborated. Further, the Phi-based redox pathway for P reduction is analysed and global multienvironmental Phi redox cycle processes are proposed on the basis of this pathway. The possible role of Phi in controlling algae in eutrophic lakes and its ecological benefits to plants are proposed. In this manner, the important role of Phi in the P redox cycle and global P cycle is systematically and comprehensively identified and confirmed. This work will provide scientific guidance for the future production and use of Phi products and arouse attention and interest on clarifying the role of Phi in the environmental phosphorus cycle.
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The COVID-19 pandemic has severely impacted public health and the worldwide economy. The overstretched operation of health systems around the world is accompanied by potential and ongoing environmental threats. At present, comprehensive scientific assessments of research on temporal changes in medical/pharmaceutical wastewater (MPWW), as well as estimations of researcher networks and scientific productivity are lacking. Therefore, we conducted a thorough literature study, using bibliometrics to reproduce research on medical wastewater over nearly half a century. Our primary goal is systematically to map the evolution of keyword clusters over time, and to obtain the structure and credibility of clusters. Our secondary objective was to measure research network performance (country, institution, and author) using CiteSpace and VOSviewer. We extracted 2306 papers published between 1981 and 2022. The co-cited reference network identified 16 clusters with well-structured networks (Q = 0.7716, S = 0.896). The main trends were as follows: 1) Early MPWW research prioritized sources of wastewater, and this cluster was considered to be the mainstream research frontier and direction, representing an important source and priority research area. 2) Mid-term research focused on characteristic contaminants and detection technologies. Particularly during 2000-2010, a period of rapid developments in global medical systems, pharmaceutical compounds (PhCs) in MPWW were recognized as a major threat to human health and the environment. 3) Recent research has focused on novel degradation technologies for PhC-containing MPWW, with high scores for research on biological methods. Wastewater-based epidemiology has emerged as being consistent with or predictive of the number of confirmed COVID-19 cases. Therefore, the application of MPWW in COVID-19 tracing will be of great interest to environmentalists. These results could guide the future direction of funding agencies and research groups.