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ABSTRACT: The spatial and temporal distributions of polycyclic aromatic hydrocarbons (PAHs) in the Songhua River, Harbin, China, were investigated. Seventy-seven samples, 42 water and 35 sediment samples, were collected in April and October of 2007 and January of 2008. The concentrations of total PAHs in water ranged from 163.54 to 2,746.25 ng/L with the average value of 934.62 ng/L, which were predominated by 2- and 3-ring PAHs. The concentrations of total 16 PAHs in sediment ranged from 68.25 to 654.15 ng/g dw with the average value of 234.15 ng/g dw, which were predominated by 4-, 5- and 6-ring PAHs. Statistical analysis of the PAH concentrations shown that the highest concentrations of the total PAHs were found during rainy season (October of 2007) and the lowest during snowy season (January of 2008). Ratios of specific PAH compounds, including fluoranthene/(fluoranthene + pyrene) (Flu/(Flu + Pyr)) and phenanthrene/(phenanthrene + anthracene) (An/(Ant + PhA)), were calculated to evaluate the possible sources of PAH contaminations. These ratios reflected pyrolytic inputs of PAHs in Songhua River water and a mixed pattern of pyrolytic and petrogenic inputs of PAHs in the Songhua River sediments. Ecotoxicological risk levels calculated for PAHs suggested that there were individual PAHs, which can less frequently cause biological impairment in some samples, but no samples had constituents that may frequently cause biological impairment. Total toxic benzo[a]pyrene equivalent of ΣcPAHs varied from 10.03 to 29.7 ng/g dw and from 0.36 to 1.92 ng/g dw for total toxic tetrachlorodibenzo-p-dioxin equivalent. The level of PAHs indicated a low toxicological risk to this area.
Environmental Geochemistry and Health 04/2013; · 1.62 Impact Factor
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ABSTRACT: Nano-scale zinc oxide (nano-ZnO) is widely used in various industrial and commercial applications. However, the available toxicological information was inadequate to assess the potential ecological risk of nano-ZnO to aquatic organisms and the publics. In this study, the developmental toxicity, oxidative stress and DNA damage of nano-ZnO embryos were investigated in the embryo-larval zebrafish, the toxicity of Zn(2+) releasing from nano-ZnO were also investigated to ascertain the relationship between the nano-ZnO and corresponding Zn(2+). Zebrafish embryos were exposed to 1, 5, 10, 20, 50, and 100mg/L nano-ZnO and 0.59, 2.15, 3.63, 4.07, 5.31, and 6.04mg/L Zn(2+) for 144h post-fertilisation (hpf), respectively. Up to 144hpf, activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx), and malondialdehyde (MDA) contents, the genes related to oxidative damage, reactive oxygen species (ROS) generation and DNA damage in zebrafish embryos were measured. The nano-ZnO was found to exert a dose-dependent toxicity to zebrafish embryos and larvae, reducing the hatching rate and inducing malformation and the acute toxicity to zebrafish embryos was greater than that of the Zn(2+) solution. The generation of ROS was significantly increased at 50 and 100mg/L nano-ZnO. DNA damage of zebrafish embryo was evaluated by single-cell gel electrophoresis and was enhanced with increasing nano-ZnO concentration. Moreover, the transcriptional expression of mitochondrial inner membrane genes related to ROS production, such as Bcl-2, in response to oxidative damage, such as Nqo1, and related to antioxidant response element such as Gstp2 were significantly down-regulated in the nano-ZnO treatment groups. However, the nano-ZnO up-regulated the transcriptional expression of Ucp2-related to ROS production. In conclusion, nano-ZnO induces developmental toxicity, oxidative stress and DNA damage on zebrafish embryos and the dissolved Zn(2+) only partially contributed to the toxicity of nano-ZnO. The adverse effects of nano-ZnO may be the important mechanisms of its toxicity to zebrafish embryos.
Aquatic toxicology (Amsterdam, Netherlands) 04/2013; 136-137C:49-59. · 3.12 Impact Factor
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ABSTRACT: Seasonal variation and influencing factors of perchlorate in snow, surface soil, rain, surface water, groundwater and corn were studied. Seven hundreds and seventy samples were collected in different periods in Harbin and its vicinity, China. Perchlorate concentrations were analyzed by ion chromatography-electrospray mass spectrometry. Results indicate that fireworks and firecrackers display from the Spring Festival to the Lantern Festival (February 2, 2011-February 17, 2011) can result in the occurrence of perchlorate in surface soil and snow. Perchlorate distribution is affected by wind direction in winter. Melting snow which contained perchlorate can dissolve perchlorate in surface soil, and then perchlorate can percolate into groundwater so that perchlorate concentrations in groundwater increased in spring. Perchlorate concentrations in groundwater and surface water decrease after rainy season in summer. Groundwater samples collected in the floodplain areas of the Songhua River and the Ashi River contained higher perchlorate concentrations than that far away with the rivers. The corns have the ability to accumulate perchlorate.
Chemosphere 12/2012; · 3.21 Impact Factor
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ABSTRACT: A comprehensive analytical method based on solid phase extraction-ion chromatography (SPE-IC) has been developed for the determination of trace perchlorate in groundwater. An amount of 0.7 liter of groundwater was enriched by a solid phase extraction column after pretreatment to remove the interference ions and then the column was eluted by 6 mL 1% NaOH solution. After filtration of the concentrated liquor with a filter membrane (0.45 microm), the liquor was analyzed on an ion chromatograph (IC) equipped with an Ion Pac AS20 separation column and a 50 microL injection loop, eluted with 40 mmol/L KOH solution. The method detection limit (MDL) and limit of determination (LOD) of perchlorate were 0.15 microg/L and 0.60 microg/L, respectively. The recovery was in the range of 99.7%-100.5% when the sampling concentrations were in the range of 1-15 microg/L. The method is economical and effective. It can be applied to determine trace perchlorate in groundwater. The perchlorate in groundwater samples got from the areas surrounding Harbin was determined by this method. The relative errors were in the range of 1.85%-9.24% between the results got by the SPE-IC and ion chromatography-tandem single quadrupole mass spectrometry.
Se pu = Chinese journal of chromatography / Zhongguo hua xue hui 01/2012; 30(1):76-9.
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ABSTRACT: The spatial and seasonal variation of polychlorinated biphenyls (PCBs) were investigated in water and sediment samples collected from Songhua River, China, from 2007 to 2008. The total concentration of PCB congeners ranged from 1.1 to 14 ng/l in water and 0.26-9.7 ng/g dry weight (dw) in sediment. The results of seasonal variation may suggest an impact to PCB concentration in water from its atmospheric input, the dilution to PCBs concentrations of high stream in summer, and a general trend towards increased volatilization in warmer conditions. From PCBs concentrations comparison between upstream and downstream of industrial urban cities, it was obvious that industrial urban cities reflect an important pollutant source for PCBs in our study, also with the evidences of high concentrations of PCBs occurring in high development industry and residential areas. Meanwhile, the homologue profile of PCBs in Songhua was analyzed, whose comparison with published data indicates that the sources of PCBs accumulated in the sediment may also came from the residue of PCBs production in China. Total five dioxin-like PCBs (CB-77, 81, 105, 114, and 126) and nine (CB-77, 81, 105, 114, 118, 123, 126, 156, and 167) were found in Songhua water and sediment.
Environmental Geochemistry and Health 11/2010; 33(3):291-9. · 1.62 Impact Factor
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ABSTRACT: The Fe2O3/TiO2/Al2O3 catalyst was prepared by using TiO2/Al2O3 as carrier and the heterogeneous photo-Fenton system was established in the three-phase fluidized bed. A fluorescence technique was developed for the determination of the hydroxyl radicals (*OH) from the heterogeneous photo-Fenton system, using coumarin as the fluorescence probe. In addition, four main factors, namely pH, H2O2 concentration, catalyst loading and UV light intensity, which could influence the concentration of OH produced during the reaction process, was also discussed. The fluorescence method using coumarin as the fluorescence probe was demonstrated to be capable of detecting *OH generated in heterogeneous photo-Fenton system with veracity and high reproducibility. It was also found that the *OH generated in heterogeneous photo-Fenton system conformed to the zero reaction dynamics in 30 min. Moreover, the pH, H2O2 concentration, catalyst loading and UV light intensity influenced the *OH generated during the reaction process.
Huan jing ke xue= Huanjing kexue / [bian ji, Zhongguo ke xue yuan huan jing ke xue wei yuan hui "Huan jing ke xue" bian ji wei yuan hui.] 09/2009; 30(9):2560-4.
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ABSTRACT: This article presents preparation, characterization and evaluation of heterogeneous Fe(III)-SiO(2) catalysts for the photo-Fenton degradation of polyacrylamide (PAM) in aqueous solution. Fe(III)-SiO(2) catalysts are prepared by impregnation method with two iron salts as precursors, namely Fe(NO(3))(3) and FeSO(4), and are characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. The irradiated Fe(III)-SiO(2) is complexed with 1,10-phenanthroline, then is measured by UV-vis-diffuse reflectance spectroscopy (UV-vis-DRS) and XPS to confirm the oxidation state of Fe in solid state. By investigating the photo-Fenton degradation of PAM in aqueous solution, the results indicate that Fe(III)-SiO(2) catalysts exhibit an excellent photocatalytic activity in the degradation of PAM. Moreover, the precursor species and the OH(-)/Fe mole ratio affect the photocatalytic activity of Fe(III)-SiO(2) catalysts to a certain extent. Finally, the amount of Fe ions leaching from the Fe(III)-SiO(2) catalysts is much low.
Journal of Hazardous Materials 06/2008; 162(2-3):860-5. · 4.17 Impact Factor
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ABSTRACT: A novel photo-catalytic reactor of three-phase internal circulation fluidized bed was employed to the photodegradation of Rhodamine B with TiO2/SiO2 carried on porous silica as photocatalyst. The degradation kinetics of Rodaming B is investigated in the reactor. It is found that the degradation of Rodaming B conform hyperbola model, the reciprocal of degradation rate 1/X is proportional to the reciprocal of time 1/t. The reaction rate constant has no relation with initial reactant concentration and is proportional to the light density and volumetric rate of energy absorption. The reaction rate conforms the experiment results quite well, the average relative error being less 3.25%.
Huan jing ke xue= Huanjing kexue / [bian ji, Zhongguo ke xue yuan huan jing ke xue wei yuan hui "Huan jing ke xue" bian ji wei yuan hui.] 12/2006; 27(11):2154-8.
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ABSTRACT: A novel three-phase internal circulating fluidized bed photocatalytic reactor was established and the radiation transformation in which was investigated. The experimental results indicate that with the interaction of gas and solid (gas flux > 0.3m3/h), the radiation transformation in the reactor along radial direction conforms to a definite exponential function, which agrees to formula Rose about the rules of light intensity distribution through evenly suspended particles. The value of radiation energy is affected by the initial light intensity, the concentration of photocatalyst and the thickness of liquid layer. The aerated gas amount only influence the state of the fluidized bed and has little effect on the distribution of light intensity along radical direction. Photocatalytic degradation of Rhodamine B indicate that the efficiency of three-phase internal circulating fluidized bed is much higher than slurry bed. The optimal catalyst concentration of this system is 10 - 12g/L.
Huan jing ke xue= Huanjing kexue / [bian ji, Zhongguo ke xue yuan huan jing ke xue wei yuan hui "Huan jing ke xue" bian ji wei yuan hui.] 02/2005; 26(1):112-6.
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ABSTRACT: A novel activated carbon coating fiber used for solid phase micro-extraction (SPME) was prepared using activated carbon powder and silica resin adhesive. The extraction properties of the novel activated carbon coating fiber were investigated. The results indicate that this coating fiber has high concentration ability, with enrichment factors for chloroform, carbon tetrachloride, trichloroethylene and tetrachloroethylene in the range of 13.8 to 18.7. The fiber is stable at temperature as high as 290 degrees C and it can be used for over 140 times at 250 degrees C. The activated carbon coating fiber was then applied to the analysis of the four halocarbon compounds mentioned above. A linear correlation with correlation coefficients between 0.995 2 and 0.999 4 and the detection limits between 0.008 and 0.05 microg/L were observed. The method was also applied to a real water sample analysis and the recoveries of these halocarbon compounds were from 95.5% to 104.6%.
Se pu = Chinese journal of chromatography / Zhongguo hua xue hui 10/2004; 22(5):547-50.