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Identification of 3-(trifluoromethyl)phenol as the malodorous compound in a pollution incident in the water supply in Catalonia (N.E. Spain) Texte intégral
2019
Quintana, Jordi | Hernández, Alejandra | Ventura, Francesc | Devesa, Ricard | Boleda, Maria Rosa
Identification of 3-(trifluoromethyl)phenol as the malodorous compound in a pollution incident in the water supply in Catalonia (N.E. Spain) Texte intégral
2019
Quintana, Jordi | Hernández, Alejandra | Ventura, Francesc | Devesa, Ricard | Boleda, Maria Rosa
A study of organic compounds that caused a serious taste and odor episode of water supply in two residential areas in Catalonia (N.E. Spain) was carried out. Sweet and paint/solvent odor were the main descriptors used by consumers. Some cases of sickness and nausea were also associated with drinking water consumption by the consumers. Closed-loop stripping analysis (CLSA) combined with sensory gas chromatography and gas chromatography mass spectrometry detection were used to study the problem. As a result, 3-(trifluoromethyl)phenol (CAS number 98-17-9) was for the first time identified as a responsible of an odor incident in drinking water. Concentration levels of this compound were up to 17,000 ng/L in groundwater and up to 600 ng/L in distributed water. Odor threshold in water for 3-(trifluoromethyl)phenol was determined as 13 ng/L (45 °C).
Afficher plus [+] Moins [-]Identification of 3-(trifluoromethyl)phenol as the malodorous compound in a pollution incident in the water supply in Catalonia (N.E. Spain) Texte intégral
2019
Quintana, Jordi | Hernández, Alejandra | Ventura, Francesc | Devesa, Ricard | Boleda, M. Rosa
A study of organic compounds that caused a serious taste and odor episode of water supply in two residential areas in Catalonia (N.E. Spain) was carried out. Sweet and paint/solvent odor were the main descriptors used by consumers. Some cases of sickness and nausea were also associated with drinking water consumption by the consumers. Closed-loop stripping analysis (CLSA) combined with sensory gas chromatography and gas chromatography mass spectrometry detection were used to study the problem. As a result, 3-(trifluoromethyl)phenol (CAS number 98-17-9) was for the first time identified as a responsible of an odor incident in drinking water. Concentration levels of this compound were up to 17,000 ng/L in groundwater and up to 600 ng/L in distributed water. Odor threshold in water for 3-(trifluoromethyl)phenol was determined as 13 ng/L (45 °C). © 2019, Springer-Verlag GmbH Germany, part of Springer Nature. | We are grateful to Dr. Auguste Bruchet for his explanations about past episodes in France involving fluoro-related compounds and to M.J. Domínguez-Cereijo for the details of the distribution system and sampling coordination. We are also grateful to all our colleagues of the Analytical Organic Chemistry Department for dealing with the daily work and spending time to move forward this study. We would also like to thank you I. Pérez and all the members and volunteers of the panel. | Peer reviewed
Afficher plus [+] Moins [-]Application of Carboxymethyl Cellulose–Stabilized Sulfidated Nano Zerovalent Iron for Removal of Cr(VI) in Simulated Groundwater Texte intégral
2019
Zhao, Lingzi | Zhao, Yongsheng | Yang, Bingjun | Teng, Honghui
Carboxymethyl cellulose–stabilized sulfidated nano zerovalent iron (CMC-S-nZVI) was tested for its capacity to the removal of Cr(VI) in this study. The effect of synthesis approaches on morphology and properties of CMC-S-nZVI was studied. Results revealed CMC-S-nZVI prepared by the surface corrosion method had favorable homogeneity and corrosion resistance. The structure and morphology of CMC-S-nZVI particles were investigated by transmission electron microscopy, X-ray powder diffraction, and Fourier-transform infrared spectrometry. Batch experiments showed that the removal efficiency of Cr(VI) by the CMC-S-nZVI particles was influenced by the S/Fe molar ratio, initial pH, initial Cr(VI) concentration, and the reaction temperature. Increasing S/Fe molar ratio from 0 to 0.35 enhanced Cr(VI) removal efficiency from 65.37 to 85.08%. Reducing pH value and improving the reaction temperature have a positive impact on Cr(VI) removal. The removal amount was 535 mg/g (total iron) CMC-S-nZVI with initial Cr(VI) concentration of 50 mg/L. Compared with CMC-nZVI, CMC-S-nZVI had better performance in Cr(VI) removal in a simulated groundwater system. The results indicated that CMC-S-nZVI might be applicable for in situ treatment of the Cr(VI)-containing groundwater.
Afficher plus [+] Moins [-]Triclosan in Treated Wastewater from a City Wastewater Treatment Plant and its Environmental Risk Assessment Texte intégral
2019
Mōhan, Es. | Balakrishnan, P.
Triclosan (TCS) is a potential endocrine-disrupting compound (EDC), which produces an adverse impact on aquatic life and human beings. Wastewater discharge is considered as the primary source of triclosan in water bodies. The study is aimed to investigate the occurrence and environmental risk of triclosan released by municipal wastewater treatment plants (WWTP). An analytical protocol was developed and validated to determine the presence of TCS in the samples through offline solid-phase extraction (SPE) and liquid chromatography - electron spray ionization (ESI)—quadrupole mass spectrum (LC/ESI/MS). The limit of detection and quantification of protocol was estimated as 2.8 ng/L and 6.25 ng/L, respectively. The season-wise influent and effluent samples from two WWTP in Chennai, India, were monitored. The TCS concentrations in samples were found in the range of 443 to 1757 ng/L. The Risk Quotient (RQ) method was performed to evaluate the environmental (ecotoxicological and human health) risk associated with the exposure of TCS-containing wastewater. The results of the study revealed that primary producer (algae) was highly vulnerable to exposure of TCS in the aquatic environment. The estimated daily intake of TCS was much lower than the reference dosage, and this indicates that TCS did not produce any considerable risk to human health. Also, it suggested that additional treatment was required for complete removal of triclosan residues.
Afficher plus [+] Moins [-]Application of modified receptor model for soil heavy metal sources apportionment: a case study of an industrial city, China Texte intégral
2019
Li, Yufeng | Zhao, Zhongqiu | Yuan, Ye | Zhu, Peitian | Li, Xuezhen | Guo, Anning | Yang, Qiao
As we all know, geochemical data usually contain outliers and they are heterogeneous, which will severely affect the use of receptor models based on classical estimates. In this paper, an advanced modified RAPCS-RGWR (robust absolute principal component scores-robust geographically weighted regression) receptor model was introduced to analyze the pollution sources of eight heavy metals (Cd, Hg, As, Pb, Ni, Cu, Zn) in a city of southern China. The results showed that source identification and source apportionment are more consistent by this advanced model even though the soil types and farming patterns are diverse. Moreover, this model decreased the occurrence of negative values of the source contribution. For these reasons, the pollution sources were classified into five types by the new model in the study area: agricultural sources, industrial sources, traffic sources, comprehensive sources, and natural sources. (1) The contributions of agricultural sources to Cr and Ni were 243.36% and 242.61%, respectively; (2) the contribution of industrial sources to Cd was 79.25%; (3) the contribution of traffic sources to Cu was 100.31%; (4) the contributions of comprehensive sources to Hg, Pb, and Zn were 253.90%, 242.31%, and 93.32%, respectively; and (5) the contribution of natural sources to As was 208.21%. Overall, the RAPCS-RGWR receptor model improved the validity of the receptor models. It is of great realistic significance to understand and popularize the advanced model in soil source apportionment in agricultural land.
Afficher plus [+] Moins [-]Manganese dioxide nanoparticles/activated carbon composite as efficient UV and visible-light photocatalyst Texte intégral
2019
Khan, Idrees | Sadiq, Muhammad | Khan, Ibrahim | Saeed, Khalid
Manganese dioxide nanoparticles/activated carbon (MnO₂/AC) composites and manganese dioxide nanoparticles (MnO₂ NPs) are prepared through chemical reduction method. Morphological study shows that MnO₂ NPs had cylindrical and spherical shape. The morphological study also revealed that MnO₂ NPs were well dispersed on AC while neat Mn NPs present both in dispersed and in agglomerated form. The FT-IR study confirms the synthesis of MnO₂ NPs. Zetasizer study presented that the Mn NPs had uniform size and below 100 nm in size and had zeta potential of − 20 mV, which represent its stability in the suspension form. The synthesized Mn/AC composite and Mn NPs were utilized as photocatalysts for the photodegradation of Congo red (CR) dye. The degradation study shows that MnO₂/AC composite degraded CR dye more efficiently than MnO₂ NPs under UV and normal light irradiation. The efficient degradation of dye by Mn/AC composite is due to the synergistic effect between dye adsorption on AC and rapid photodegradation by supported MnO₂ NPs. The results revealed that Mn/AC composite degraded about 98.53% of CR dye within 5 min while MnO₂ NPs degraded 66.57% of dye within the same irradiation time. The recycled catalyst also significantly degraded dye which verifies its sustainability. The effect of catalyst dosage and initial dye concentration was conducted. The degradation rate of dye was found drastically faster in tap water (in presence of catalyst), which might be due to the presence of various mineral ions in the tap water.
Afficher plus [+] Moins [-]Increasingly Distant from Eden—a Look at the Soils of Protected Areas Using Ecotoxicological Tests and Chemical Analysis Texte intégral
2019
Honscha, Laiz Coutelle | de Moura, Renata Rodrigues | Baisch, Paulo Roberto Martins | Da Silva Júnior, Flavio Manoel Rodrigues
On the basis of the assumption that legally protected areas are created to maintain environmental quality that, in turn, is indispensable for quality of life, this study aims to evaluate the soil conditions in protected areas that are located near urban regions by using ecotoxicological assays and chemical analysis. The study was carried out using surface soil samples collected from seven protected areas in southern Brazil. For the protected area to be considered “clean,” the results of the ecotoxicological tests should be within the criteria accepted for negative control according to standardized protocols, and the concentration of chemical elements should be below the maximum levels allowed by Brazilian law. On the basis of the criteria adopted for ecotoxicological assays and chemical analysis, soil from only two of the seven protected areas (28.6%) met the criteria for being considered “clean.” This probably reflects the influence of anthropogenic activities within the protected areas, demonstrating drawbacks of delimitation and management. The strategy used in this study could be used to assess the anthropogenic impact on protected areas in other parts of the world.
Afficher plus [+] Moins [-]Residue concentrations and profiles of PCDD/Fs in ash samples from multiple thermal industrial processes in Vietnam: Formation, emission levels, and risk assessment Texte intégral
2019
Pham, Mai Thi Ngoc | Hoang, Anh Quoc | Nghiem, Xuan Truong | Tu, Binh Minh | Dao, Thi Nhung | Vu, Duc Nam
The residue concentrations and congener profiles of polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) were examined in fly ash and bottom ash released from different thermal industrial processes in Vietnam. PCDD/F concentrations and toxic equivalents (TEQs) in the ash samples varied greatly and decreased in the following order: steel making > aluminum recycling > medical waste incinerator > boilers > municipal waste incinerator > tin production > brick production > coal-fired power plant. Both the precursor and de novo synthesis were estimated as possible formation mechanisms of dioxins in the ash, but the latter pathway was more prevalent. The highest emission factors were estimated for the ash released from some steel-making plants, aluminum-recycling facilities, and a medical waste incinerator. The emission factors of PCDD/Fs in ash released from some steel plants of this study were two to six times higher than the UNEP Toolkit default value. The annual emission amount of ash-bound dioxins produced by 15 facilities in our study was estimated to be 26.2 to 28.4 g TEQ year⁻¹, which mainly contributed by 3 steel plants. Health risk related to the dioxin-containing ash was evaluated for workers at the studied facilities, indicating acceptable risk levels for almost all individuals. More comprehensive studies on the occurrence and impacts of dioxins in waste streams from incineration and industrial processes and receiving environments should be conducted, in order to promote effective waste management and health protection scheme for dioxins and related compounds in this rapidly industrializing country.
Afficher plus [+] Moins [-]Study on new artificial floating island removing pollutants Texte intégral
2019
Kong, Lingwei | Wang, Lu | Wang, Qirui | Mei, Rongwu | Yang, Yifan
In this study, two types of artificial floating islands (AFIs), group A (consists of 1# and 2# traditional AFIs with plant and soil) and group B (consists of 4# and 5# new-type AFIs with plant, substrate, and with luffa sponge and corncob hanging at the bottom), were constructed, respectively. The removal effects and degradation mechanisms of luffa sponge and corncob in group B were compared and investigated. Plant height, root growth, and packing degradation of the two types of AFIs were studied. Temperature, dissolved oxygen (DO), and pH on the decontamination effects of AFI were discussed. The results showed that group A and group B AFIs showed great significant differences in removal of CODCᵣ, TN, NO₃⁻−N, NH₄⁺−N, and TP (p < 0.05). The TP removal of group B was 92.8 ± 0.6%, and the TN removal and NO₃⁻−N removal were significantly higher than that of group A, which was 90.3 ± 0.8% and 96.0 ± 2.2%, respectively; The addition of luffa sponge and corncob could enhance the biodegradability of sewage and the nitrogen and phosphorus removal efficiency of group B. The plant growth height of group B planted with Lythrum salicaria was 2.36 times higher than that of group A. The effect of temperature on TP was significantly greater than that of TN, and both groups of AFIs presented continuous improvement capacities of TN and TP removal when the temperature was above 15 °C. Group B was observed with a lower pH range of 6.69~7.12, which was more suitable for denitrification than group A. The release of carbon source of 5#-corncob AFI was 2.51 times higher than 4#-luffa sponge AFI at the end of the experiment.
Afficher plus [+] Moins [-]Advanced SiO2 Composite Materials for Heavy Metal Removal from Wastewater Texte intégral
2019
Olteanu, Marius | Baraitaru, Andreea | Panait, Ana-Maria | Dumitru, Diana | Boboc, Mădălina | Deák, György
Thermal processing of materials is used in a very broad sense to cover all sets of technologies and processes for a wide range of industrial sectors and it refers to material development with a specific application potential due to its advantages over conventional synthesis methods. By applying hydrothermal technique, the development of advanced materials has been pursued, in order to retain heavy metals from wastewater. This research refers to nanosilica-based materials, specifically mesoporous silica, for which the heavy metal retention properties were improved by using nano-TiO₂ and nano-CeO₂, considering the properties of titanium and cerium. Advanced methods have been used to characterize the materials obtained as X-ray fluorescence (XRF) and energy-dispersive X-ray spectroscopy (EDS) for chemical composition; X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) for microstructural properties and BET analyser for pores and specific surface area characterization. The results showed higher retention efficiencies for the doped nanosilica.
Afficher plus [+] Moins [-]Influence of electronic cigarette vaping on the composition of indoor organic pollutants, particles, and exhaled breath of bystanders Texte intégral
2019
van Drooge, Barend L. | Marco, Esther | Perez, Noemi | Grimalt, Joan O.
Influence of electronic cigarette vaping on the composition of indoor organic pollutants, particles, and exhaled breath of bystanders Texte intégral
2019
van Drooge, Barend L. | Marco, Esther | Perez, Noemi | Grimalt, Joan O.
The changes of particles and organic pollutants in indoor atmospheres as consequence of vaping with electronic cigarettes have been analyzed. Changes in the composition of volatile organic compounds (VOCs) in exhaled breath of non-smoking volunteers present in the vaping environments have also been studied. The exposure experiments involved non-vaping (n = 5) and vaping (n = 5) volunteers staying 12 h together in a room (54 m²) without external ventilation. The same experiment was repeated without vaping for comparison. Changes in the distributions of particles in the 8–400 nm range were observed, involving losses of nucleation-mode particles (below 20 nm) and increases of coagulation processes leading to larger size particles. In quantitative terms, vaping involved doubling the indoor concentrations of particles smaller than 10 μm, 5 μm, and 1 μm observed during no vaping. The increase of particle mass concentrations was probably produced from bulk ingredients of the e-liquid exhaled by the e-cigarette users. Black carbon concentrations in the indoor and outdoor air were similar in the presence and absence of electronic cigarette emissions. Changes in the qualitative composition of PAHs were observed when comparing vaping and non-vaping days. The nicotine concentrations were examined separately in the gas and in the particulate phases showing that most of the differences between both days were recorded in the former. The particulate phase should therefore be included in nicotine monitoring during vaping (and smoking). The concentration increases of nicotine and formaldehyde were small when compared with those described in other studies of indoor atmospheres or health regulatory thresholds. No significant changes were observed when comparing the concentrations of exhaled breath in vaping and no vaping days. Even the exhaled breath nicotine concentrations in both conditions were similar. As expected, toluene, xylenes, benzene, ethylbenzene, and naphthalene did not show increases in the vaping days since combustion was not involved.
Afficher plus [+] Moins [-]Influence of electronic cigarette vaping on the composition of indoor organic pollutants, particles, and exhaled breath of bystanders Texte intégral
2019
Van Drooge, Barend L. | Marco, Esther | Pérez, Noemí | Grimalt, Joan O. | European Commission | Van Drooge, Barend L. [0000-0002-6434-3390] | Marco, Esther [0000-0002-9870-3470] | Grimalt, Joan O. [0000-0002-7391-5768]
The changes of particles and organic pollutants in indoor atmospheres as consequence of vaping with electronic cigarettes have been analyzed. Changes in the composition of volatile organic compounds (VOCs) in exhaled breath of non-smoking volunteers present in the vaping environments have also been studied. The exposure experiments involved non-vaping (n = 5) and vaping (n = 5) volunteers staying 12 h together in a room (54 m 2 ) without external ventilation. The same experiment was repeated without vaping for comparison. Changes in the distributions of particles in the 8–400 nm range were observed, involving losses of nucleation-mode particles (below 20 nm) and increases of coagulation processes leading to larger size particles. In quantitative terms, vaping involved doubling the indoor concentrations of particles smaller than 10 μm, 5 μm, and 1 μm observed during no vaping. The increase of particle mass concentrations was probably produced from bulk ingredients of the e-liquid exhaled by the e-cigarette users. Black carbon concentrations in the indoor and outdoor air were similar in the presence and absence of electronic cigarette emissions. Changes in the qualitative composition of PAHs were observed when comparing vaping and non-vaping days. The nicotine concentrations were examined separately in the gas and in the particulate phases showing that most of the differences between both days were recorded in the former. The particulate phase should therefore be included in nicotine monitoring during vaping (and smoking). The concentration increases of nicotine and formaldehyde were small when compared with those described in other studies of indoor atmospheres or health regulatory thresholds. No significant changes were observed when comparing the concentrations of exhaled breath in vaping and no vaping days. Even the exhaled breath nicotine concentrations in both conditions were similar. As expected, toluene, xylenes, benzene, ethylbenzene, and naphthalene did not show increases in the vaping days since combustion was not involved. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature. | Funding Partial funding from EU projects HEALS (FP7-ENV-2013-603946), NEUROSOME (H2020-MSCA-ITN-2017 SEP-210411486), and EPPA S.A has been received. | Peer reviewed
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