共查询到20条相似文献,搜索用时 15 毫秒
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采用高效液相色谱法对太湖梅梁湾水体中微囊藻毒素的质量浓度进行春、夏、秋、冬4个季节的监测,分析了梅梁湾水体中微囊藻毒素(MC-RR,MC-YR,MC-LR)质量浓度的季节变化特征及其与水体中总氮、总磷、CODMn和浮游藻类等富营养化指标的相关关系。分析结果表明:MCs夏季(8月份)质量浓度最高,为(0.78±0.99)μg.L-1,其次为春季(5月份)和秋季(11月份),分别为(0.43±0.96)和(0.50±1.12)μg.L-1,冬季(2月份)质量浓度显著降低,为(0.14±0.27)μg.L-1;水体中MCs的检出质量浓度与常规水化学指标之间相关性分析表明:MC-LR的质量浓度与TP的质量浓度呈极显著正相关与TN/TP呈极显著负相关(P〈0.01),与CODMn呈显著正相关(P〈0.05);水体中MCs的检出质量浓度与浮游藻类生物量相关性分析表明:水体中MCs的检出质量浓度与微囊藻及蓝藻生物量有显著相关关系,太湖梅梁湾的藻毒素主要由微囊藻属(Microcystis)产生。 相似文献
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Xue BAI Hanchang SHI Zhengfang YE Qiujin SUN Qing WANG Zhongyou WANG 《Frontiers of Environmental Science & Engineering》2013,7(6):844-850
In this study, microorganisms (named B111) were immobilized on polyvinyl alcohol microspheres prepared by the inverse suspension crosslinked method. The biodegradation of bisphenol A (BPA) and 4-hydro- xybenzaldehyde, a degradation product of BPA, by free and immobilized B lll was investigated. The BPA degradation studies were carried out at initial BPA concentrations ranging from 25 to 150 mg·L^-1. The affinity constant Ks and maximum degradation rate Rmax were 98.3 mg·L^-1 and 19.7mg·mg^-1VSS·d^-1 for free B111, as well as 87.2mg·L^-1 and 21.1mg·mg^-1VSS·d^-1 for immobilized B 111, respectively. 16S rDNA gene sequence analyses confirmed that the dominant genera were Pseudomonas and Brevundimonas for BPA biodegradation in microorganisms B 111. 相似文献
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Haitao WANG 《Frontiers of Environmental Science & Engineering》2013,7(6):833-835
The outdoor smog chamber was used to thorough investigate the rate constants of gas-phase reaction between dimethyl sulfide (DMS) and ozone (O3) under conditions of relative humidity 55.0%-67.8% at (296±2)K for the first time. The rate constants were measured, at a total pressure of 1 atm, to be (10.4±0.2) × 10^-19 cm^3·molecule^-1·s^-1 at relative humidity of 67.5%±0.3% at 298K, (10.1±0.1) × 10^-19cm^3·molecule^-1·s^-1 at relative humidity of 66.5%±0.5% at 296K, (7.75±0.39) × 10^-19cm^3·molecule^-1·s^-1 at relative humidity of 64.8%± 0.1% at 294K and (3.42±0.21) × 10^-19cm^3·molecu- le^-1·s^-1at relative humidity of 55.8%±0.8% at 295K. Base on these results, it is possible to see the reaction of O3/ DMS in the presence of water vapor as an important sink for DMS in the earth atmosphere. 相似文献
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Xiaoyan MA Shifei HU Hongyu WANG Jun LI Jing HUANG Yun ZHANG Weigang LU Qingsong LI 《Frontiers of Environmental Science & Engineering》2012,6(2):171-176
Metabolites of algae such as geosmin, 2-methylisoborneol etc. are reported to induce pungent odors into drinking water and attract additional scientific attention. Recently, in China, taste and odor outbreaks in drinking water supply have become increasingly common. In source water affected by eutrophication, dimethyl trisulfide, speculated to be produced by decayed algae, was found to be the source of taste and odor issues and can be removed effectively by usual oxidation agents. In this experimental study, batch scale tests were carried out focusing on the removal of dimethyl trisulfide. Reaction kinetics of dimethyl trisulfide oxidized by potassium permanganate in water had been studied; influence factors such as pH, organic substrate, other existed taste, and odor contaminant in equivalent concentration were also discussed. Results showed that dimethyl trisulfide can be removed by potassium permanganate efficiently; the ratio can reach more than 70% with oxidant dosage of 4 mg·L-1 and contact time prolonged to 120 min. The dimethyl trisulfide decomposition followed a second-order kinetics pattern with a rate constant k = 0.00213 L·(min·mg)-1. Typically, the degradation rate of dimethyl trisulfide was increased with the increasing KMnO4 dosage, but dramatically dropped with the increasing levels of humic acid (1.8–4.5 mg·L-1) and other odor-causing compounds (e.g. β -cyclocitral, 0–1886.0 μg·L-1). Solution pH (5.2–9.0) and initial dimethyl trisulfide concentration did not significantly affected the degradation. This study demonstrates that KMnO4 oxidation is an effective option to remove dimethyl trisulfide from water. 相似文献
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太湖蓝藻水华及其次级代谢产物微囊藻毒素(MCs)的生物累积对生态系统和人体健康造成严重威胁,已成为最近环境科学研究的热点。本研究从太湖的不同区域(梅梁湖、西部沿岸区、南部沿岸区和湖心区)采集不同体重和体长的白鲢,利用固相萃取方法提取、高效液相色谱-质谱联用仪测定了白鲢不同器官中MCs的3种异构体MC-RR、MC-YR及MC-LR的含量,结合不同湖区的相关水质指标分析了MCs在白鲢体内的累积规律及其影响因素。研究结果表明:白鲢不同器官MCs的含量由高到低为:肠壁肾脏肝脏肌肉心脏,且肠壁累积的MCs显著高于肾脏、肝脏、肌肉和心脏。MC-RR含量是白鲢各器官累积MCs的异构体的主体,约占MCs的60%。梅梁湖鲢鱼的肌肉、肾脏和心脏中MCs均高于西部沿岸区、南部沿岸区和湖心区。生物指标(体重和体长)是影响白鲢肾脏内MCs和MC-RR含量以及肠壁内MCs含量重要因素。太湖水质指标总磷(TP)、藻细胞数量、湖泊营养指数及环节动物数量尤其是TP对白鲢肝脏累积MCs产生明显影响,TP、总氮(TN)、铵态氮(NH4-N)、内梅罗指数和环节动物数量尤其是NH4-N对肠壁累积MCs产生明显影响。 相似文献
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Tianyi Li Chengwu Zhang Jingyi Zhang Song Yan Chuanyu Qin 《Frontiers of Environmental Science & Engineering》2021,15(5):87
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Jingke Song Chenyang Li Xuejiang Wang Songsong Zhi Xin Wang Jianhui Sun 《Frontiers of Environmental Science & Engineering》2021,15(6):129
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于2017年冬季12月13—21日在青藏高原东缘理塘地区分昼夜采集PM2.5样品,并用DRI2001A热光碳分析仪测定了有机碳(OC)和元素碳(EC)的质量浓度,研究青藏高原PM2.5中碳组分的化学特征及主要来源,以期为理塘地区制定污染排放政策提供参考。结果表明,2017年冬季青藏高原东缘理塘地区PM2.5平均质量浓度为44.34μg·m?3,OC和EC的质量浓度为12.72μg·m?3和3.85μg·m?3,分别占PM2.5质量浓度的29.61%和8.96%。通过经验公式,计算得到总碳气溶胶(TCA)质量浓度为24.20μg·m?3,占PM2.5的54.84%,说明碳质气溶胶对青藏高原东缘理塘地区PM2.5有着十分重要的贡献。OC和EC在白天和夜间都有较高的相关性(相关系数分别为0.74和0.91),表明OC和EC的来源基本一致,受燃烧源影响较大。其中白天的相关系数低于夜间,说明青藏高原东缘理塘地区白天碳组分来源相对复杂。昼夜浓度对比显示,青藏高原东缘理塘地区PM2.5白天和夜间的质量浓度分别为53.88μg·m?3和33.44μg·m?3,OC和EC浓度白天高于夜间,表明白天人为排放相对较高。冬季观测期间,PM2.5中二次有机碳(SOC)昼夜浓度分别为1.11μg·m?3和3.03μg·m?3,分别占OC质量浓度的7.09%、26.59%,表明青藏高原东缘理塘城区白天碳组分主要为一次源。利用PMF 5.0软件对理塘城区碳组分进行进一步的解析,结果显示燃煤和生物质燃烧的混合源对总碳(TC)的贡献高达47.84%,占比最高;其次是汽车尾气和柴油车尾气源,贡献率分别为28.62%和23.54%。 相似文献
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Wenyue Li Min Chen Zhaoxiang Zhong Ming Zhou Weihong Xing 《Frontiers of Environmental Science & Engineering》2020,14(6):102
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为研究中国典型沿海城市冬季PM2.5中碳组分的污染特征及来源,于2018年12月5日—2019年1月30日分别在天津(TJ)、上海(SH)和青岛(QD)同步采集PM2.5样品。结果表明,天津、上海和青岛PM2.5的平均浓度分别为(116.96±66.93)、(31.21±25.62)、(74.93±54.60)μg·m-3,OC和EC的空间分布均为天津(18.69±7.95)μg·m-3和(4.98±2.08)μg·m-3>青岛(16.45±8.94)μg·m-3和(2.01±1.04)μg·m-3>上海(7.28±3.11)μg·m-3和(1.05±1.25)μg·m-3。3个站点的OC和EC均呈现较好的相关性,表明OC和EC具有相似的来源;OC/EC比值范围在2.37—7.53、5.47—46.41和4.77—13.36之间,证明各采样点均存在二次有机碳(SOC)的生成;采用最小R2法(MRS)估算SOC浓度,得到3个采样点SOC的平均质量浓度为(5.09±4.68)、(3.90±1.65)、(4.21±4.31)μg·m-3,分别占OC总量的27.2%、55.8%和19.5%,其中上海的SOC在OC中的占比最大,说明上海二次有机碳污染较为严重,这主要归因于冬季严重污染源排放和有利的二次转化气象条件,而天津和青岛的碳组分主要来自污染源的直接排放。主成分分析(PCA)结果发现,天津PM2.5中碳组分主要来源于道路尘、生物质燃烧和机动车尾气,上海PM2.5中碳组分主要来源于生物质燃烧、道路扬尘和机动车尾气。青岛PM2.5中碳组分主要来源于道路扬尘、机动车尾气。后向轨迹聚类分析表明,来自西北方向的气团对天津的影响较大,PM2.5和碳组分的浓度值最大;而对上海而言,主要受北方气溶胶经过海面又传输回上海的气团的影响;青岛站点主要受华北地区污染物和本地排放源的影响。 相似文献
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Qi YING 《Frontiers of Environmental Science & Engineering》2011,5(3):348-361
The UCD/CIT model was modified to include a process analysis (PA) scheme for gas and particulate matter (PM) to study the formation of secondary nitrate aerosol during a stagnant wintertime air pollution episode during the California Regional PM2.5/PM10 Air Quality Study (CRPAQS) where detailed measurements of PM components are available at a few sites. Secondary nitrate is formed in the urban areas from near the ground to a few hundred meters above the surface during the day with a maximum modeled net increase rate of 4 μg·m-3·d-1 during the study episode. The secondary nitrate formation rate in rural areas is lower due to lower NO2. In the afternoon hours, near-surface temperature can be high enough to evaporate the particulate nitrate. In the nighttime hours, both the gas phase N2O5 reactions with water vapor and the N2O5 heterogeneous reactions with particle-bound water are important for secondary nitrate formation. The N2O5 reactions are most import near the surface to a few hundred meters above surface with a maximum modeled net secondary nitrate increase rate of 1 μg·m-3·d-1 and are more significant in the rural areas where the O3 concentrations are high at night. In general, vertical transport during the day moves the nitrate formed near the surface to higher elevations. During the stagnant days, process analysis indicates that the nitrate concentration in the upper air builds up and leads to a net downward flux of nitrate through vertical diffusion and a rapid increase of surface nitrate concentration. 相似文献
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Xufang Wang Dongli Guo Jinna Zhang Yuan Yao Yanbiao Liu 《Frontiers of Environmental Science & Engineering》2023,17(9):106
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Xiaoliang WANG Curtis ROBBINS S. Kent HOEKMAN Judith C. CHOW John G. WATSON Dennis SCHUETZLE 《Frontiers of Environmental Science & Engineering》2011,5(3):320-330
Thermochemical biomass gasification, followed by conversion of the produced syngas to fuels and electrical power, is a promising energy alternative. Real-world characterization of particulate matter (PM) and other contaminants in the syngas is important to minimize damage and ensure efficient operation of the engines it powers and the fuels created from it. A dilution sampling system is demonstrated to quantify PM in syngas generated from two gasification plants utilizing different biomass feedstocks: a BioMax?15 Biopower System that uses raw and torrefied woodchips as feedstocks, and an integrated biorefinery (IBR) that uses rice hulls and woodchips as feedstocks. PM2.5 mass concentrations in syngas from the IBR downstream of the purification system were 12.8–13.7 μg·m-3, which were significantly lower than the maximum level for catalyst protection (500 μg·m-3) and were 2–3 orders of magnitude lower than those in BioMax?15 syngas (2247–4835 μg·m-3). Ultrafine particle number concentration and PM2.5 chemical constituents were also much lower in the IBR syngas than in the BioMax?15. The dilution sampling system enabled reliable measurements over a wide range of concentrations: the use of high sensitivity instruments allowed measurement at very low concentrations (~1 μg·m-3), while the flexibility of dilution minimized sampling problems that are commonly encountered due to high levels of tars in raw syngas (~1 g·m-3). 相似文献