排序方式: 共有6条查询结果,搜索用时 0 毫秒
1
1.
Ivančev-Tumbas Ivana Lužanin Zorana Česen Marjeta Bogunović Minja Sekulić Tatjana Djaković Heath David Heath Ester 《Environmental science and pollution research international》2021,28(42):59368-59381
Environmental Science and Pollution Research - This study reports how adding a membrane filter (0.45-μm cellulose nitrate filter) between a glass fibre filter and the solid phase extraction... 相似文献
2.
3.
de Nazelle A Nieuwenhuijsen MJ Antó JM Brauer M Briggs D Braun-Fahrlander C Cavill N Cooper AR Desqueyroux H Fruin S Hoek G Panis LI Janssen N Jerrett M Joffe M Andersen ZJ van Kempen E Kingham S Kubesch N Leyden KM Marshall JD Matamala J Mellios G Mendez M Nassif H Ogilvie D Peiró R Pérez K Rabl A Ragettli M Rodríguez D Rojas D Ruiz P Sallis JF Terwoert J Toussaint JF Tuomisto J Zuurbier M Lebret E 《Environment international》2011,37(4):766-777
4.
Kožul D Herceg Romanić S Kljaković-Gašpić Z Veža J 《Environmental monitoring and assessment》2011,179(1-4):325-333
Levels of 24 organochlorine compounds were investigated in wild mussels collected at two locations (Krka estuary and Ka?tela Bay) on the Croatian Adriatic coast in 2003, 2005, 2006, 2007, and 2008. PCB and OCP ranges found at the two locations overlapped and followed similar profiles despite the differences between the two locations indicating that they share a common pollutants source. Among organochlorine pesticides, the dominant compound was DDT. Among indicator PCBs, the dominant compound was PCB-153, while PCB-118 was dominant among the remaining 11 congeners. Generally, the sum of six indicator PCBs was constantly greater than the sum of 11 congeners at both locations. α-HCH/γ-HCH and DDE/DDT ratios were below 1, indicating recent input of γ-HCH and DDT into the marine environment. In the investigated period, almost all organochlorine compounds reached the highest values in 2006. The levels of PCBs and OCPs in this study were considerably below the Croatian maximum permissible levels, confirming that they do not pose any threat for human health. 相似文献
5.
Zorana Kljaković-Gašpić Snježana Herceg Romanić Tomislav Bituh Vilena Kašuba Irena Brčić Karačonji Nataša Brajenović Iva Franulović Jasna Jurasović Darija Klinčić Nevenka Kopjar Gordana Marović Mirta Milić Tatjana Orct Ankica Sekovanić Davor Želježić 《Environmental monitoring and assessment》2018,190(11):694
In this study, the influence of anthropogenic pollution on the aquatic environment of Plitvice Lakes National Park (PLNP) was investigated during 2011–2012 using a combination of chemical and cytogenetic analyses. Four groups of major contaminants [(volatile organic compounds: benzene, toluene, ethylbenzene, and xylenes (BTEX); persistent organochlorine pollutants: organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs); major and trace elements; anthropogenic radionuclides (90Sr, 134Cs, and 137Cs)] were determined in three aquatic compartments (water, sediment, fish). Mass fractions of inorganic constituents in different compartments reflected the geological background of the area, indicating their origin from predominantly natural sources. Levels of volatile and persistent organic compounds in water and fish, respectively, were very low, at levels typical for remote pristine areas. Analysis of anthropogenic radionuclides in water and sediment revealed elevated activity concentrations of 137Cs in water, and measurable 134Cs in the upper sediment layers from April 2011, possibly as a consequence of the Fukushima nuclear accident in March 2011. The potential genotoxicity of river and lake water and lake sediment was assessed under laboratory conditions using the alkaline comet assay on human peripheral blood lymphocytes, and measured levels of primary DNA damage were within acceptable boundaries. The results showed that despite the protected status of the park, anthropogenic impact exists in both its terrestrial and aquatic components. Although contaminant levels were low, further monitoring is recommended to make sure that they will not rise and cause potentially hazardous anthropogenic impacts. 相似文献
6.
Rabih Sa Zorana Radovic-Hrapovi Behzad Ahvazi Sonia Thiboutot Guy Ampleman Jalal Hawari 《环境科学学报(英文版)》2012,24(5):808-813
The present study describes the use of two commercially available lignins, namely, alkali and organosolv lignin, for the removal of 2,4-dinitroanisole (DNAN), a chemical widely used by the military and the dye industry, from water. Sorption of DNAN on both lignins reached equilibrium within 10 hr and followed pseudo second-order kinetics with sorption being faster with alkali than with organosolv lignin, i.e. k2 10.3 and 0.3 g/(mg hr), respectively. In a separate study we investigated sorption of DNAN between 10 and 40°C and found that the removal of DNAN by organosolv lignin increased from 0.8 to 7.5 mg/g but reduced slightly from 8.5 to 7.6 mg/g in the case of alkali lignin. Sorption isotherms for either alkali or organosolv lignin best fitted Freundlich equation with enthalpy of formation, ΔH0 equaled to 14 or 80 kJ/mol. To help understand DNAN sorption mechanisms we characterized the two lignins by elemental analysis, BET nitrogen adsorption-desorption and 31P NMR. Variations in elemental compositions between the two lignins indicated that alkali lignin should have more sites (O- and S-containing functionalities) for H-bonding. The BET surface area and calculated total pore volume of alkali lignin were almost 10 times greater than that of organosolv lignin suggesting that alkali lignin should provide more sites for sorption. 31P NMR showed that organosolv lignin contains more phenolic -OH groups than alkali lignin, i.e., 70% and 45%, respectively. The variations in the type of OH groups between the two lignins might have affected the strength of H-bonding between DNAN and the type of lignin used. 相似文献
1