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Ferronato Navarro Moresco Luca Guisbert Lizarazu Gabriela Edith Gorritty Portillo Marcelo Antonio Conti Fabio Torretta Vincenzo 《Environmental science and pollution research international》2023,30(4):8548-8562
Environmental Science and Pollution Research - Construction and demolition waste (CDW) and municipal solid waste (MSW) are the waste flows mostly generated at a global level. In developing... 相似文献
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Jéssica Manfrin Daniel Schwantes Affonso Celso Gonçalves Jr. Michelli Caroline Ferronato Valdemir Aleixo Andréia da Paz Schiller 《Environmental monitoring and assessment》2018,190(4):243
Due to intense agricultural and industrial activities, the environment has been affected by increasing amounts of pollutants, such as lead, a toxic heavy metal. When introduced to the environment, toxic metals are distributed and incorporated into the liquid medium, sediments, and aquatic biota; bioaccumulating. This research aimed to identify and quantify the levels of toxic metals present in the waters and sediments of Toledo River, compare the obtained results with legislation and other studies, as well as to evaluate the possible pollutant sources of the water body. Six water and sediment samples were taken at seven strategic sites. The concentrations of Cu, Zn, Fe, Mn, Cd, Pb, and Cr in water were compared to the maximum limits established by Brazilian legislation IN CONAMA No. 357/05, for class II fresh waters. The sediment samples were submitted to nitroperchloric digestion, and then the total concentrations of the metals were determined by flame atomic absorption spectrometry (FAAS). The toxicological quality of the Toledo River has been considerably affected by the activities carried out in its surroundings, such as extensive areas of agriculture, pig farming and industrial areas, causing concentrations of Cd, Fe, and mainly Pb, which is observed at concentrations higher than value allowed by the legislation. 相似文献
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Lei Zhou Mohamad Sleiman Corinne Ferronato Jean-Marc Chovelon Claire Richard 《Environmental Chemistry Letters》2017,15(4):733-737
Advanced oxidation processes based on sulfate radicals (SO 4 ·? ) are capable of efficiently degrade organic pollutants from ground, surface and wastewaters. However, this degradation may be limited by aqueous natural organic matter (NOM). Here we measured the absolute rate constants of reaction of SO 4 ·? with four types of organic matter: two fulvic acids and two lake organic matter. We used laser flash photolysis technique to monitor the SO 4 ·? decay and the formation of the transients from organic matters. Reaction rate constants comprised between 1530 and 3500 s?1 mgC?1 L were obtained by numerical analysis of differential equations and the weighted average of the extinction coefficient of the generated organic matters radicals between 400 and 800 M?1 cm?1. 相似文献
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Rada Elena Cristina Ionescu Gabriela Ferronato Navarro Ragazzi Marco Raspanti Mario Conti Fabio Torretta Vincenzo 《Environmental science and pollution research international》2021,28(42):59076-59082
Environmental Science and Pollution Research - In the present paper, different types of pure and commercial plastic waste from different EU countries (UK, France, Italy, and Romania) were... 相似文献
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Nitrate-induced photodegradation of atenolol in aqueous solution: kinetics, toxicity and degradation pathways 总被引:2,自引:0,他引:2
The extensive utilization of β-blockers worldwide led to frequent detection in natural water. In this study the photolysis behavior of atenolol (ATL) and toxicity of its photodegradation products were investigated in the presence of nitrate ions. The results showed that ATL photodegradation followed pseudo-first-order kinetics upon simulated solar irradiation. The photodegradation was found to be dependent on nitrate concentration and increasing the nitrate from 0.5 mM L−1 to 10 mM L−1 led to the enhancement of rate constant from 0.00101 min−1 to 0.00716 min−1. Hydroxyl radical was determined to play a key role in the photolysis process by using isopropanol as molecular probe. Increasing the solution pH from 4.8 to 10.4, the photodegradation rate slightly decreased from 0.00246 min−1 to 0.00195 min−1, probably due to pH-dependent effect of nitrate-induced OH formation. Bicarbonate decreased the photodegradation of ATL in the presence of nitrate ions mainly through pH effect, while humic substance inhibited the photodegradation via both attenuating light and competing radicals. Upon irradiation for 240 min, only 10% reduction of total organic carbon (TOC) can be achieved in spite of 72% transformation rate of ATL, implying a majority of ATL transformed into intermediate products rather than complete mineralization. The main photoproducts of ATL were identified by using solid phase extraction-liquid chromatography-mass spectrometry (SPE-LC-MS) techniques and possible nitrate-induced photodegradation pathways were proposed. The toxicity of the phototransformation products was evaluated using aquatic species Daphnia magna, and the results revealed that photodegradation was an effective mechanism for ATL toxicity reduction in natural waters. 相似文献
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Ji Yuefei Yang Yan Wang Lu Lu Junhe Ferronato Corinne Chovelon Jean-Marc 《Environmental Chemistry Letters》2019,17(2):1111-1116
Environmental Chemistry Letters - Sulfate radical ( $${\text{SO}}_{4}^{ \cdot - }$$ )-based advanced oxidation processes (SR-AOPs) are promising in situ chemical oxidation technologies that... 相似文献
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Brigante M Emmelin C Ferronato C Greca MD Previtera L Paisse JO Chovelon JM 《Chemosphere》2007,68(3):464-471
The effect of positional isomerism on chemical and photochemical degradations of the Imazamethabenz-methyl (IMBM), a pesticide of the imidazolinone family, has been studied. IMBM is proposed in the form of a mixture of the two positional isomers: meta and para. The development of an effective HPLC method (resolution factor R=1.3) allows us to follow either the abiotic disappearance of the meta and para IMBM and the formation of their breakdown products. The abiotic degradation studies include the chemical hydrolysis, as well as the direct and the indirect photodecomposition. We used TiO(2), a well-known initiator of hydroxyl radicals, to highlight the role of *OH in the indirect photodegradation. This work confirms the different behaviours of positional isomers in the environment. Indeed the chemical or direct photochemical degradation is faster for the meta isomer than for the para. Whereas, concerning IMBM, there is not any prevalent influence of this type of isomerism on the indirect photochemical degradation. The degradation products were tentatively identified by LC-MS, NMR and IR and a degradation pathway was proposed. 相似文献
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