东北地区臭氧预氧化对常规净水工艺效果分析

为检验臭氧预氧化在北方地区的效果,结合东北地区某微污染水源做出了分析和探索,发现臭氧氧化对净水处理效果良好。并全面阐述了微污染水源采用臭氧预氧化技术后带来的效果,可用于脱色除臭、控制氯化消毒副产物、去除藻类和藻毒素、助凝和助滤、初步去除或转化污染物,为相关的工程设计奠定了基础。     

“十一五”期间通辽市环境质量存在的主要问题及成因

本文通过对＂十一五＂期间通辽市环境质量监测数据的统计分析,从污染源和环境质量的关系得出存在的问题,从自然环境要素与生态环境两个角度总结＂十一五＂期间存在的问题。通过对环境质量的问题分析,寻找产生这些问题的原因,从而为改善环境质量提供解决的途径。     

Variation of low molecular weight organic acids in precipitation and cloudwater at high elevation in South China

To investigate the sources and chemical behaviors of carboxylic acids in Southern China, precipitation and corresponding cloudwater samples were collected in an acid rain-prone area of Mount Heng. The carboxylic acid levels in the samples were measured, and the concentration patterns were evaluated with respect to temporal and seasonal variations. Formic and acetic acids were predominant among the carboxylic acids identified for both precipitation and cloudwater. Most of the organic acids in the precipitation had a clear seasonal pattern, reaching higher levels during the warm season; these higher levels were attributed to the stronger source strength of biogenic emissions during this season. The cloud–fog samples did not display a similar trend. A distinctive diurnal pattern in carboxylic acids was only observed in the precipitation samples during the warm season. In cloud–fog, the ratio of formic to acetic acid differed considerably with time, with these values varying little in the precipitation samples. This result indicates that the organic acids in precipitation originate consistently from primary sources throughout the entire period, while those in cloud are mainly associated with direct emissions in the earlier stage and with secondary sources in the later period.     

Sources, distribution, and risk assessment of organochlorine pesticides in Nairobi City, Kenya

The distribution and sources of organochlorine pesticides (OCPs) in air and surface waters were monitored in Nairobi City using triolein-filled semipermeable membrane devices (SPMDs). The SPMDs were extracted by dialysis using n-hexane, followed by cleanup by adsorption chromatography on silica gel cartridges. Sample analysis was done by GC-ECD and confirmed by GC–MS. Separation of means was achieved by analysis of variance, followed by pair-wise comparison using the t-test (p≤ 0.05). The total OCPs ranged between 0.018 – 1.277 ng/m³ in the air and <LOD – 1391.000 ng/m³ in surface waters. Based on the results, the means of Industrial Area, Dandora and Kibera were not significantly different (p≤ 0.05), but were higher (p≤ 0.05) than those of City square and Ngong’ Forest. The results revealed non-significant (p≤ 0.05) contribution of long-range transport to OCP pollution in Nairobi City. This indicated possible presence of point sources of environmental OCPs in the city. The water-air fugacity ratios indicated that volatilization and deposition played an important role in the spatial distribution of OCPs in Nairobi City. This indicated that contaminated surface waters could be major sources of human exposure to OCPs, through volatilization. The incremental lifetime cancer risks (ILCR) determined from inhalation of atmospheric OCPs were 2.3745  ×  10^?13 – 1.6845  ×  10^?11 (adult) and 5.5404  ×  10^?13 – 3.9306  ×  10^?11 (child) in the order: Dandora > Kibera > Industrial Area > City Square > Ngong’ Forest. However, these were lower than the USEPA acceptable risks, 10^?6 – 10^?4. This study concluded that atmospheric OCPs did not pose significant cancer risks to the residents.     

农业非点源污染环境影响及防治

非点源污染也称面源污染,因其污染的时空范围广,不确定性大,污染严重,对其治理及管理的难度也较大.由于化肥和农药的大量使用,农业非点源已成为中国水环境的主要污染源.文章中对农业非点源污染的特点、来源和危害进行了系统论述,并提出防治农业非点源污染的具体措施建议.     

气溶胶中多环芳烃的污染源识别方法

文章评述了气溶胶中多环芳烃污染源类型识别的几种方法,即:比值法、轮廓图法、特征化合物法和多元统计方法等.比值法简单可行,应用较多,但常因苯并(a)芘的不稳定性而带来误差,建议与轮廓图法、特征化合物法等配合使用,多元统计法要求样品数多,并且运算复杂,目前应用尚不多见,但其潜力很大。      

大通湖主要污染物浓度空间分布及其污染来源解析

为了解大通湖主要污染物TN、TP和NH3-N的空间分布特征及污染来源,于2017年9月对大通湖及周边河流进行采样分析。结果表明,大通湖周边入湖河流的ρ(TN)为0. 74～2. 18 mg/L,ρ(NH3-N)为0. 094～0. 874 mg/L,ρ(TP)为0. 02～0. 243 mg/L;湖体ρ(TN)为0. 82～1. 47 mg/L,呈现湖体中间低、四周高的特征,ρ(NH3-N)为0. 14～0. 42 mg/L,但整体差异较大,高值区主要在大通湖西南及东部,ρ(TP)为0. 160～0. 289 mg/L,水质为Ⅴ类或劣Ⅴ类,TP为湖体的主要污染物,湖体的ρ(TP)变化呈现出从四周向中部增加的趋势,高值区主要集中在大通湖正南及湖心处;根据2016年大通湖区域污染源统计及入湖污染物计算,大通湖水环境的TP污染负荷大小排序为农田径流畜禽养殖生活污水工业污染网箱养鱼旅游服务。     

丹东市环境空气SO_2总量控制初探

采用GB13201-91中的大气污染物总量控制方法总量计算公式,计算丹东市建成区环境空气SO2总量及污染状况。结果表明,整个采暖季全市SO2总量不需要削减,但低架源排放污染物较多,应进行削减。     

PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) in Beijing: Seasonal variations, sources, and risk assessment

Polycyclic aromatic hydrocarbons(PAHs) have been of health concern due to its carcinogenesis and mutagenesis. In this study, we aimed to assess the variations, sources, and lifetime excessive cancer risk(ECR) attributable to PAHs bound to ambient particulate matters with aerodynamic diameter less than 2.5 μm(PM_(2.5)) in metropolitan Beijing, China. We collected24-hour integrated PM_(2.5) samples on daily basis between November 2014 and June 2015 across both central heating(cold months) and non-heating(warm months) seasons, and further analyzed the PAH components in these daily PM_(2.5) samples. Our results showed that total concentrations of PM_(2.5)-bound PAHs varied between(88.6 ± 75.4) ng/m~3 in the cold months and(11.0 ± 5.9) ng/m~3 in the warm months. Benzo[a]pyrene(Ba P), the carcinogenic marker of PAHs,averaged at 5.7 and 0.4 ng/m~3 in the cold and warm months, respectively. Source apportionment analyses illustrated that gasoline, biomass burning, diesel, coal combustion and cooking were the major contributors, accounting for 12.9%, 17.8%, 24.7%, 24.3% and 6.4% of PM_(2.5)-bound PAHs, respectively. The BaP equivalent lifetime ECR from inhalation of PM_(2.5)-bound PAHs was 16.2 cases per million habitants. Our results suggested that ambient particulate reduction from energy reconstruction and adaption of clean fuels would result in reductions PM_(2.5)-bound PAHs and its associated cancer risks. However, as only particulate phased PAHs was analyzed in the present study, the concentration of ambient PAHs could be underestimated.     

Catchment soils as a factor of trace metal accumulation in sediments of the reservoir Klingenberg (eastern Ore Mountains, Germany)

The release and accumulation dynamics of trace metals in soils and aquatic sediments were exemplarily investigated in the catchment area of the Reservoir Klingenberg(Germany). Catchment soils were examined for mobilizable and total concentrations of arsenic(As), cadmium(Cd), chrome(Cr), iron(Fe), manganese(Mn), nickel(Ni), lead(Pb),and zinc(Zn) and compared with trace metal quantities accumulated in riverbed and reservoir sediments. The comparison of all samples showed relatively small variations of Cr(7.96–46.0 mg/kg), Fe(7.79–40.4 g/kg), and Ni(6.06–56.5 mg/kg), while stronger differences were found for As(11.2–164 mg/kg), Cd(0.14–30.5 mg/kg), Mn(0.08–1.84 g/kg), Pb(20.7–183 mg/kg), and Zn(69.1–916 mg/kg). The catchment soils were slightly enriched by Cd, Pb, and Zn. Especially Cd and Zn were characterized by large mobilizable proportions.The mean trace metal concentrations in riverbed sediments were higher than in catchment soils, while reservoir sediments accumulated the highest amounts of the analyzed elements. The enrichment of trace metals in reservoir sediments was generally determined by the sedimentation of fine particles, while the distribution of As, Fe, and Mn was additionally impacted by redox conditions. For Cd and Zn, which in comparison were most enriched in riverbed and reservoir sediments, a significant release from soils by leaching processes was observed. The accumulation of As and Pb in reservoir sediments was influenced to a greater extent by soil erosion and by anthropogenic or chalcogen sources in the catchment.