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171.
Mendes Telmo José Siqueira Diego Silva de Figueiredo Eduardo Barretto Bordonal Ricardo de Oliveira Moitinho Mara Regina Marques Júnior José La Scala Jr. Newton 《Environment, Development and Sustainability》2021,23(11):16410-16427
Environment, Development and Sustainability - Soils feature significant variations in soil carbon stocks through land-use changes, management practices, and intrinsic characteristics. The aim of... 相似文献
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173.
T. Valente M. J. Rivera S. F. P. Almeida C. Delgado P. Gomes J. A. Grande M. L. de la Torre M. Santisteban 《Environmental science and pollution research international》2016,23(7):6002-6011
This work presents a combination of geochemical, mineralogical, and biological data obtained in water reservoirs located in one of the most paradigmatic mining regions, suffering from acid mine drainage (AMD) problems: the Iberian Pyrite Belt (IPB). Four water reservoirs located in the Spanish sector of the IBP, storing water for different purposes, were selected to achieve an environmental classification based on the effects of AMD: two mining dams (Gossan and Águas Ácidas), a reservoir for industrial use (Sancho), and one with water used for human supply (Andévalo). The results indicated that the four reservoirs are subject to the effect of metallic loads from polluted rivers, although with different levels: Águas Ácidas > Gossan > Sancho ≥ Andévalo. In accordance, epipsammic diatom communities have differences in the respective composition and dominant taxa. The dominant diatoms in each reservoir indicated acid water: Pinnularia acidophila and Pinnularia aljustrelica were found in the most acidic dams (Gossan and Águas Ácidas, with pH <3), Pinnularia subcapitata in Sancho (pH 2.48–5.82), and Eunotia exigua in Andévalo (pH 2.34–6.15). 相似文献
174.
Petrick A. Soares Tânia F. C. V. Silva Diego R. Manenti Selene M. A. G. U. Souza Rui A. R. Boaventura Vítor J. P. Vilar 《Environmental science and pollution research international》2014,21(2):932-945
Different advanced oxidation processes (AOPs) were applied to the treatment of a real cotton-textile dyeing wastewater as a pre-oxidation step to enhance the biodegradability of the recalcitrant compounds, which can be further oxidized using a biological process. Tests were conducted on a lab-scale prototype using artificial solar radiation and at pilot scale with compound parabolic collectors using natural solar radiation. The cotton-textile dyeing wastewater presents a lilac color, with a maximum absorbance peak at 641 nm, alkaline pH (pH?=?8.2), moderate organic content (DOC?=?152 mg C L?1, COD?=?684 mg O2 L?1) and low-moderate biodegradability (40 % after 28 days in Zahn–Wellens test). All the tested processes contributed to an effective decolorization and mineralization, but the most efficient process was the solar-photo-Fenton with an optimum catalyst concentration of 60 mg Fe2+ L?1, leading to 98.5 % decolorization and 85.5 % mineralization after less than 0.1 and 5.8 kJUV L?1, respectively. In order to achieve a final wastewater with a COD below 250 mg O2 L?1 (discharge limit into water bodies imposed by the Portuguese Legislation-Portaria no. 423/97 of 25 June 1997), considering the combination of a solar-photo-Fenton reaction with a biological process, the phototreatment energy required is 0.5 kJUV L?1, consuming 7.5 mM hydrogen peroxide, resulting in 58.4 % of mineralization $ \left({t}_{30\mathrm{W}}=3.2\ \min; \overline{T}=30.7\ {}^{\circ}\mathrm{C};\overline{\mathrm{pH}}=2.80;{\overline{\mathrm{UV}}}_{G,n}={13\ \mathrm{W}\ \mathrm{m}}^{-2}\right). $ 相似文献
175.
Milena Petriccione Valentina Forte Diego Valente Claudia Ciniglia 《Environmental science and pollution research international》2013,20(7):4859-4871
Catechol is a highly toxic organic pollutant, usually abundant in the waste effluents of industrial processes and agricultural activities. The environmental sources of catechol include pesticides, wood preservatives, tanning lotion, cosmetic creams, dyes, and synthetic intermediates. Genotoxicity of catechol at a concentration range 5?×?10?1–5 mM was evaluated by applying random amplified polymorphic DNA (RAPD) and time-lapse DNA laddering tests using onion (Allium cepa) root cells as the assay system. RAPD analysis revealed polymorphisms in the nucleotidic sequence of DNA that reflected the genotoxic potential of catechol to provoke point mutations, or deletions, or chromosomal rearrangements. Time-lapse DNA laddering test provided evidence that catechol provoked DNA necrosis and apoptosis. Acridine orange/ethidium bromide staining could distinguish apoptotic from necrotic cells in root cells of A. cepa. 相似文献
176.
The dynamic light scattering (DLS) technique can detect the concentration and size distribution of nanoscale particles in aqueous solutions by analyzing photon interactions. This study evaluated the applicability of using photon count rate data from DLS analyses for measuring levels of biogenic and manufactured nanoscale particles in wastewater. Statistical evaluations were performed using secondary wastewater effluent and a Malvern Zetasizer. Dynamic light scattering analyses were performed equally by two analysts over a period of two days using five dilutions and twelve replicates for each dilution. Linearity evaluation using the sixty sample analysis yielded a regression coefficient R(2) = 0.959. The accuracy analysis for various dilutions indicated a recovery of 100 ± 6%. Precision analyses indicated low variance coefficients for the impact of analysts, days, and within sample error. The variation by analysts was apparent only in the most diluted sample (intermediate precision ~12%), where the photon count rate was close to the instrument detection limit. The variation for different days was apparent in the two most concentrated samples, which indicated that wastewater samples must be analyzed for nanoscale particle measurement within the same day of collection. Upon addition of 10 mg l(-1) of nanosilica to wastewater effluent samples, the measured photon count rates were within 5% of the estimated values. The results indicated that photon count rate data can effectively complement various techniques currently available to detect nanoscale particles in wastewaters. 相似文献
177.
P. Gayán C.R. Forero L.F. de Diego A. Abad F. García-Labiano J. Adánez 《International Journal of Greenhouse Gas Control》2010,4(1):13-22
Chemical-Looping Combustion (CLC) is an emerging technology for CO2 capture because separation of this gas from the other flue gas components is inherent to the process and thus no energy is expended for the separation. Natural or refinery gas can be used as gaseous fuels and they may contain different amounts of light hydrocarbons. This paper presents the combustion results obtained with a Cu-based oxygen carrier using mixtures of CH4 and light hydrocarbons (LHC) (C2H6 and C3H8) as fuel. The effect on combustion efficiency of the fuel reactor temperature, solid circulation flow rate and gas composition was studied in a continuous CLC plant (500 Wth). Full combustions were reached at 1073 and 1153 K working at oxygen to fuel ratios, ? higher than 1.5 and 1.2 respectively. Unburnt hydrocarbons were never detected at any experimental conditions at the fuel reactor outlet. Carbon formation can be avoided working at 1153 K or at ? values higher than 1.5 at 1073 K. After 30 h of continuous operation, the oxygen carrier exhibited an adequate behavior regarding attrition and agglomeration. It can be concluded that no special measures should be taken in a CLC process with Cu-based OC with respect to the presence of LHC in the fuel gas. 相似文献
178.
Heitor Evangelista Juan Maldonado Elaine A. dos Santos Ricardo H.M. Godoi Carlos A.E. Garcia Virginia M.T. Garcia Erling Jonhson Kenya Dias da Cunha Carlos Barros Leite René Van Grieken Katleen Van Meel Yaroslava Makarovska Diego M. Gaiero 《Atmospheric environment (Oxford, England : 1994)》2010,44(5):703-712
Iron (Fe) and other trace elements such as Zn, Mn, Ni and Cu are known as key-factors in marine biogeochemical cycles. It is believed that ocean primary productivity blooms in iron deficient regions can be triggered by iron in aeolian dust. Up to now, scarce aerosol elemental composition, based on measurements over sea at the Western South Atlantic (WSA), exist. An association between the Patagonian semi-desert dust/Fe and chlorophyll-a variability at the Argentinean continental shelf is essentially inferred from models. We present here experimental data of Fe enriched aerosols over the WSA between latitudes 22°S–62°S, during 4 oceanographic campaigns between 2002 and 2005. These data allowed inferring the atmospheric Fe flux onto different latitudinal bands which varied from 30.4 to 1688 nmolFe m?2 day?1 (October 29th–November 15th, 2003); 5.83–1586 nmolFe m?2 day?1 (February 15th–March 6th, 2004) and 4.73–586 nmolFe m?2 day?1(October 21st–November 5th, 2005). 相似文献
179.
180.
Townsend-Small A Pataki DE Tseng LY Tsai CY Rosso D 《Journal of environmental quality》2011,40(5):1542-1550
Nitrous oxide (N?O) is a long-lived and potent greenhouse gas produced during microbial nitrification and denitrification. In developed countries, centralized water reclamation plants often use these processes for N removal before effluent is used for irrigation or discharged to surface water, thus making this treatment a potentially large source of N?O in urban areas. In the arid but densely populated southwestern United States, water reclamation for irrigation is an important alternative to long-distance water importation. We measured N?O concentrations and fluxes from several wastewater treatment processes in urban southern California. We found that N removal during water reclamation may lead to in situ N?O emission rates that are three or more times greater than traditional treatment processes (C oxidation only). In the water reclamation plants tested, N?O production was a greater percentage of total N removed (1.2%) than traditional treatment processes (C oxidation only) (0.4%). We also measured stable isotope ratios (δN and δO) of emitted N?O and found distinct δN signatures of N?O from denitrification (0.0 ± 4.0 ‰) and nitrification reactors (-24.5 ± 2.2 ‰), respectively. These isotope data confirm that both nitrification and denitrification contribute to N?O emissions within the same treatment plant. Our estimates indicate that N?O emissions from biological N removal for water reclamation may be several orders of magnitude greater than N?O emissions from agricultural activities in highly urbanized southern California. Our results suggest that wastewater treatment that includes biological nitrogen removal can significantly increase urban N?O emissions. 相似文献