南京市溧水区大气挥发性有机物污染特征及来源解析

为了解南京市溧水区大气挥发性有机物(VOCs)的组分、来源及其对臭氧的贡献,2021年对区域内VOCs开展了为期1 a的走航监测,进行数据分析.结果表明,溧水区ρ(TVOC)年均值为223.45μg·m^-3,其中ρ(烷烃)为49.45μg·m^-3(占比22.13%),ρ[含氧(氮)VOCs]为50.63μg·m^-3(占比22.66%),ρ(卤代烃)为64.73μg·m^-3(占比28.95%),ρ(芳香烃)为35.46μg·m^-3(占比15.87%),ρ(烯烃)为18.26μg·m^-3(占比8.19%),其他为4.9μg·m^-3(占比2.2%).夏季的ρ(TVOC)平均值较高,为263.75μg·m^-3,冬季较低,为187.2μg·m^-3,春季为246.11μg·m^-3,秋季为204.77μg·m^-3.日均TVOC浓度,在09:00～10:00和14...     

广东东江流域多氯萘的大气沉降研究

为考察多氯萘(PCNs)通过大气沉降作用对东江流域的影响,利用通用型大气沉降采样器,在东江流域广东省境内代表性地段布设11个采样点,于2010年冬季(1、2月)和夏季(7、8月)分别采集和分析了沉降样品中PCNs的通量及组成.结果表明,东江流域总PCNs日均沉降通量为828 pg.(m2.d)-1,对应毒性当量(TEQ)为0.14 pg.(m2.d)-1,由此估算东江流域广东境内PCNs年沉降总量为8.5 kg,相应TEQ年沉降总量为1.3 g.地域上,广州和东莞地区沉降通量明显高于惠州,同时城镇采样点的沉降通量显著高于农村;季节上,各采样点总体呈现夏季高于冬季的特点;组成上,三氯萘(tri-CNs)是主要的污染物,占总量的50%以上,但广州、东莞的5～8氯萘含量比惠州高.来源分析表明,东江流域PCNs的大气沉降可能受燃烧源与非燃烧源的共同影响;东莞大气沉降中PCNs多来自燃烧源,广州点大气沉降的PCNs以非燃烧源为主.     

Impacts of invasive plants on ecosystems in natural reserves in Jiangsu of China

To estimate the impacts of invasive plants on ecosystems, a survey has been conducted in three sites including both buffer zones and core zones. 13, 19 species are found in the Yuntai Mountain and Longchi Mountain natural reserve respectively, and 23 in the Purple Mountain Natural Park. Altogether 25 species belonging to 12 families, the majority of which are native to North America, some of them have set up stable reproducible populations. Among them, Solidago canadensis is found in Longchi Mountain and Purple Mountain. Communities of Galinsoga parviflora, Gynura crepidioides, Ageratum conyzoides, and Ambrosia artemisiifolia pose a serious threat to local biodiversity.     

柴油机微粒中可溶性有机成分的真空干燥条件

柴油机碳烟颗粒(PM)中可溶性有机组分(SOF)含量是其重要的特性参数,而真空干燥法可方便、高效、可靠地分析颗粒SOF含量,对其干燥条件的探索具有重要的研究意义和应用价值。首先采用模拟的柴油机颗粒,分析不同的干燥条件对模拟SOF(柴油、润滑油)挥发率的影响规律,得出模拟的SOF分析的最佳干燥条件;在此基础上,探索了真实柴油机颗粒SOF分析的最佳干燥条件为:干燥温度220℃、干燥时间3 h、真空度98 kPa,得知SOF组分干燥的难易程度介于柴油和润滑油之间;同时,根据此干燥条件,分析了排气管末端采集的真实碳烟颗粒的SOF含量特性。     

Extraction of heavy metals from e-waste contaminated soils using EDDS

Environmental contamination due to uncontrolled e-waste recycling activities is drawing increasing attention in the world. Extraction of these metals with biodegradable chelant [S,S]-ethylenediaminedisuccinic acid (EDDS) and the factors influencing extraction efficacy were investigated in the present study. Results showed that the addition of EDDS at low pH (5.5) produced higher metal extraction than that at high pH (8.0) solution. Metal speciation analysis indicated that Cu was completely complexed with EDDS at different pH conditions with various amounts of EDDS applied. For Pb and Zn, at low EDDS dose of 0.304 mol/kg soil, they were present as Pb- and Zn-EDDS. However, at high EDDS dose of 1.26 mol/kg soil, most of Pb was bound with dissolved organic matter. Ca and Al were found to be strong competitors for trace metals to EDDS at low application dose and low pH condition.     

速灭菊酯在水稻-水-鱼系统中的动态

采用同位素示踪技术和模拟生态系统试验法,对水田施用速灭菊酯后对邻近水域的污染、水域中鱼类对速灭菊酯残留物的浓缩和排除等进行了研究,结果表明,在田表水中,残留物浓度随处理后时间而迅速降低。水系中淤泥对水中残留物有明显的吸附净化作用,鱼对水中速灭菊酯残留物的摄取和排除均很迅速。 用二室模型对速灭菊酯残留物在田表水中的消失、用一级输入和输出的单室模型对鱼体中残留物浓度随时间的变化动态研究表明,在田表水中,土壤对水中残留物起着强烈的吸附净化作用;在水系中,鱼体中残留物浓度的消长主要取决于残留物自身在水中的消失速率,只是在前期同时依赖于鱼体对残留物的排除效应,鱼体的摄入常数只对鱼体累积浓度最大值及到达最大值的时间T_m产生影响。     

Evaluation of solubility of polycyclic aromatic hydrocarbons in ethyl lactate/water versus ethanol/water mixtures for contaminated soil remediation applications

Solubility data of recalcitrant contaminants in cosolvents is essential to determine their potential applications in enhanced soil remediation. The solubilities of phenanthrene, anthracene, fluoranthene and benzo[a]pyrene in ethyl lactate/water and ethanol/water mixtures were measured using equilibrium techniques. The cosolvency powers derived from solubility data were then applied to the model developed from the solvophobic approach to predict the capability of ethyl lactate and ethanol in enhancing the desorption of contaminants from soils. Both ethyl lactate and ethanol cosolvents were shown to be able to enhance the solubilisation of the tested four polycyclic aromatic hydrocarbons by > 4 orders of magnitude above the levels obtained with water alone. However, ethyl lactate demonstrated a greater capacity to enhance PAH solubility than ethanol. The cosolvency powers of ethyl lactate/water system obtained from the end-to-end slope (σ) and the end-to-half slope (σ_0.5) of the solubilisation curve were 1.0--1.5 and 2.0--2.9 higher than ethanol/water system respectively. In line with this, ethyl lactate/water was demonstrated to enhance the desorption of contaminants from soil by 20%--37% and 18%--61% higher compared to ethanol/water system in low organic content and high organic content soils respectively, with a 2:1 (V/W) ratio of solution:soil and with cosolvent fraction as low as 0.4. With the exception of benzo[a]pyrene, the experimental desorption results agreed fairly with the predicted values, under an applied solution:soil ratio that was enough to hold the capacity of released contaminants.     

Hexabromocyclododecanes in surface sediments and a sediment core from Rivers and Harbor in the northern Chinese city of Tianjin

In the present study, hexabromocyclododecanes (HBCDs) were investigated in the sediment from Haihe River (HR), Dagu Dainage Canal (DDC) and Tianjin Harbor (TH) at Bohai Bay using a total of 51 samples of surface sediments and a sediment core collected from May to September in 2010, and its diastereomer- and enantiomer-specific profiles were analyzed. The concentration of total HBCDs were generally high, with mean value and ranges of 31.0 and 1.35–634 ng g^?1 dw, respectively. The contamination followed the order of TH > DDC > HR. Higher levels (up to 634 ng g^?1 dw) occurred in the lower reach of HR and DDC located in an industrial area of Tianjin. This is the first time to report so high concentration of HBCDs in sediment in Southeast Asia. The γ-diastereomer dominated in most samples (44 out of 51), and this is in agreement with the diastereomer distribution pattern in industrial products, while α-HBCD was the dominant diastereomer in the other seven samples. However, only few samples exhibited γ-diastereomer ratio similar to that (75–89%) in technical products, indicating the inter-transformation and variable degradation of the different isomers. The high ratio of γ-diastereomer could be used as an indicator for fresh contamination input. Enantiomeric factors (EFs) of HBCD isomers in most of the samples were statistically different from technical products (p < 0.05), showing a trend of more easily enrichment of the (?)-HBCD-enantiomer compared to the (+)-HBCD-enantiomer. The δ- and ε-diastereomers were frequently detected but at low level. The HBCDs in the sediment core showed several peaks, and the greatest value occurred in 2005, when a plastic manufacture plant using HBCD was set up nearby.     

Hexabromocyclododecanes in limnic and marine organisms and terrestrial plants from Tianjin,China: Diastereomer- and enantiomer-specific profiles,biomagnification, and human exposure

To interpret the distribution of hexabromocyclododecanes (HBCDs) in various organisms, we measured the concentrations and diastereomer and enantiomer profiles of HBCDs in 21 different species of limnic and marine cohorts from Tianjin, China. The concentration ranges of HBCDs in limnic and marine organisms were 64.3–1111 ng g⁻¹ lw and 85.5–989 ng g⁻¹ lw, respectively. Living habitat and feeding habits had important impacts on HBCD diastereomer distribution. Most of the species appeared to preferentially select (+)-α-, (−)-β- and (−)-γ-HBCD. There is a tendency that the total and α-HBCDs were magnified as trophic level increased with trophic magnification factors (TMFs) around 2. The concentrations of HBCDs in the limnic and marine fishes were highest in the liver, followed by the gill, skin, and muscle. In terrestrial plants, the highest concentrations of HBCDs were observed in the leaf, followed by the root and the rhizosphere soil. Plants showed enantioselectivity for HBCD enantiomers, which varied with plant species and organs (leaf vs. root) of the same plant. Higher estimated daily intakes (EDIs) of HBCDs were observed from fish than from wheat.     

黄渤海表层沉积物中正构烷烃和甾醇的分布及来源研究

在黄海、渤海湾和莱州湾采集64个表层沉积物样品,分析正构烷烃（C15～C33）和甾醇（菜子甾醇、菜油甾醇、谷甾醇和豆甾醇）的质量分数和分子组合特征,探讨其来源,比较物质来源的空间差异。结果表明：（1）黄海表层沉积物中类脂生物标志物主要呈现陆源和海源共同影响的特征,其中北黄海以陆源输入为主,高碳数正构烷烃（〉C24）具有明显的奇碳优势,陆源高等植物的贡献较大;南黄海陆源输入与海洋自身贡献相当;渤海湾与莱州湾接受来自河流的大量陆源物质;（2）来源于陆源高等植物的甾醇（包括菜油甾醇、谷甾醇和豆甾醇）在黄海表层沉积物中的质量分数远小于渤海湾和莱州湾,但指示硅藻来源的菜子甾醇在整个研究区域均具有较高的质量分数。