捕集阱顶空-气相色谱/质谱法检测地表水中25种挥发性有机物

建立了捕集阱顶空-气相色谱/质谱法检测地表水中25种挥发性有机物的分析方法。采用正交实验设计对捕集阱顶空条件进行了优化,该方法相关系数0.995,加标回收率为90%~110%,方法检出限为0.08~0.39μg/L,相对标准偏差(n=7)为0.7%~4.8%,仪器检出限低于0.04μg/L。方法准确度和灵敏度较好,可以满足对地表水中25种挥发性有机物的检测要求。     

长江口区域水体半挥发性有机污染物健康风险评价

近年来长江口区域水体的有机物污染日渐严重.主要应用美国环境保护局(USEPA)的健康风险评价方法,并对其进行了一定的修改和补充,对长江口区域水体半挥发性有机污染物的健康风险进行了初步评价.结果表明:长江口区域水体半挥发性有机污染物的非致癌风险指数均小于1,其中单环芳香族类的非致癌风险值均在10-3数量级,卤代烃类的风险值在10-4数量级,均偏高于其他类物质;各类物质的致癌风险指数均在10-4数量级以下,其中六氯苯、双(2-氯乙基)醚和咔唑的风险指数相对较高,在10-5数量级.根据USEPA的建议值,初步认为目前长江口区域水体中单一半挥发性有机污染物不会对人体产生明显的健康危害.由于缺少相关的研究资料,因此各种有机污染物的联合健康效应评价尚无法进行.      

Transformations of particles, metal elements and natural organic matter in different water treatment processes

Characterizing natural organic matter （NOM）, particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Preozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon （GAC） filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant （HPAC） was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.     

西江溶解有机碳的输送对典型洪水过程的响应

对2005年6月西江干流出现特大洪水期间及其前后的溶解有机碳(DOC)进行连续采样分析.结果表明,DOC浓度对流量变化的响应不敏感(n=43,R2=0.23,p＞0.05),尽管流量有6～7倍的变化,但DOC浓度的变化不到30%.洪水前夕、洪水期间及洪水过后DOC平均浓度逐渐降低,且洪水过后西江下游各个采样点的DOC浓度明显低于洪水前夕.DOC的输出量主要受地表径流深度的影响,二者之间存在着显著的线性相关关系.DOC荷载通量与流量密切相关,通过建立二者之间的线性回归方程可以计算出DOC的输出量,洪水期间DOC的输出量为4.5×1010g.     

Organochlorine compounds and polycyclic aromatic hydrocarbons in surface sediment from Baiyangdian Lake, North China： Concentrations, sources profiles and potential risk

Organochlorine pesticides(OCPs),polychlorinated biphenyls(PCBs),and polycyclic aromatic hydrocarbons(PAHs) were determined in nineteen surface sediment samples collected from Baiyangdian Lake and its inflowing river(Fuhe River) in North China.Total concentrations of OCPs,PCBs and PAHs in sediments ranged from 5.4 to 707.6 ng/g,2.3 to 197.8 ng/g,and 101.3 to 6360.5 ng/g,respectively.The levels of contaminants in Fuhe River were significantly higher than those in Baiyandian Lake.For hexachlorocyclohexane(HCHs) and dichlorodiphenytrichloroethanes(DDTs),α-HCH and p,p-DDT were predominant isomers;while for PCBs,PCB 28/31,PCB 40/103,PCB 60,PCB 101,and PCB 118 were predominant congeners.Possible sources derived from historical usage for OCPs and incomplete combustion fuel,wood,and coal and exhaustion of boats or cars for PAHs.Risk assessment of sediment indicated that sediments in Fuhe River were likely to pose potential biological adverse impact.     

海洋酸化与重金属、有机污染物和人工纳米颗粒的联合毒性效应研究进展

由于大量人类活动的影响,大气CO_2浓度持续增加,其中约1/3被海洋吸收,导致表层海水pH值降低和碳酸盐平衡体系波动,即"海洋酸化"现象。污染物的海洋环境效应一直是全球环境科学领域研究的热点。在实际环境中,海洋酸化往往与污染物共同存在并作用于海洋生态系统,且海洋酸化极有可能改变污染物的海洋环境行为从而影响其毒性效应。但现有研究大多针对海洋酸化或者污染物单独作用下的毒性效应展开,对海洋酸化与污染物的联合毒性效应的研究不足、亟待加强。为此,综述了近年来海洋酸化与典型污染物(重金属、有机污染物)及新型污染物(人工纳米颗粒)的相关文献,重点阐述了海洋酸化对污染物环境行为的影响和海洋酸化与污染物对海洋生物的联合毒性效应,指出当前的研究不足,并对未来的研究方向进行了展望。     

可离子化有机污染物对大型溞的毒性及QSAR研究

取代苯酚、苯胺和苯甲酸类化合物是在环境水体中具有较强生物毒性的芳香族可离子化有机化合物,它们在水体中对水生生物和水生生态系统都有较大危害。测定此类化合物在p H值为6、7.8和9的条件下对大型溞的24 h急性毒性,计算化合物在不同p H值条件下的中性态分子所占比例F0。研究毒性与F0的相关性,结果表明F0对取代苯酚和苯甲酸类化合物的毒性的影响较大而对取代苯胺毒性的影响很小。对于卤代苯甲酸类化合物,毒性与疏水性的相关性较好,但是羟基苯甲酸类化合物的毒性与疏水性参数的相关性很差,引入量子化学参数EHOMO和取代羟基个数NOH,可以改进苯甲酸类化合物的模型的质量。     

典型喀斯特城市湖库溶解性有机质成分特征及来源解析

为探索喀斯特城市湖库溶解性有机质（DOM）成分特征及来源信息,以我国贵阳市重要喀斯特湖库——红枫湖、百花湖、松柏山水库和阿哈水库为研究对象,分析了表层水体溶解性有机碳（DOC）、叶绿素a（Chla）和DOM光学参数(a₂₅₄、a₂₈₀、a₃₅₀、 E2∶E3、S_275-295、 FI、β:α、 BIX、 HIX)的空间差异,同时利用荧光吸收峰（B、 T、 A、 M、 C、 D、 N）和三维荧光平行因子分析（EEM-PARAFAC）解释DOM各成分丰度及占比状况,并运用Spearman相关分析及主成分分析（PCA）揭示DOM参数的相关性和主要环境过程.结果表明,喀斯特城市湖库ρ（DOC）和ρ（Chla）范围分别为4.24～11.9 mg·L^-1和0.32～19.7μg·L^-1,松柏山水库腐殖质(a₂₅₄)和芳香类蛋白质(a₂₈₀)较高,导致相对分子质量(E2∶E3和S_275-295)高于其它湖...     

Transformation of Organic Matter of the Larch Forest Soils in the Northern Taiga of Nizhne-Tungusskoe Plateau, Central Siberia

The evaluation of biospheric role of the boreal forests in the accumulation of carbon is connected with the evaluation of organic matter (OM) pool in soils. The research sites were larch forests, they are situated on Nizhne-Tungusskoe Plateau. Larch forests of feather-moss and lichen types (110 and 380 years old) were formed on 'ochric podbur' soils. Litter stocks are 3.5–4.5 kg m^{− 2} with thickness 10–25 cm. Cryomezomorphic northern taiga soils contains 38–73 t (carbon) ha^{− 1}. Pool of fast mineralized OM has average value 38.1 t (carbon) ha^{− 1}, including 20.5 and 6.4 t (Carbon) ha^{− 1} of labile compounds on surface and in the soil, and 11.2 t (carbon) ha^{− 1} of mobile OM. Microbial mass reaches 1.78–3.47 t (carbon) ha^{− 1}, its proportion is 3.6–4.9% of the total OM carbon. Zoomass of feather-moss larch forest is 0.20–0.61 * 10^{− 2}, in lichen larch forest −0.01–0.07 * 10^{− 2} t (carbon) ha^{− 1}. A pool of resistant to biological decomposition and bonded to mineral soil matrix OM is 17.7 t (carbon) ha^{− 1} and it varies from 18.6 to 29.0 in feather-moss larch forest, and from 6.4 to 17.0 t (carbon) ha^{− 1} in lichen larch forest. Two-years field experiment has been performed to determine transformation rates of various plant litter fractions and to clarify the role of soil biota in these processes. The results showed participation of all biota groups in the decomposition of plant residues caused weight loss of larch-needles and root mortmass. Isolation of organic matter from all-size invertebrate groups leads to some decrease of decomposition activity.     

氯化对二级处理出水中溶解性有机物结构的影响

以哈尔滨市W污水处理厂污水为研究对象,利用XAD树脂对二级处理出水中的溶解性有机物(DOM)进行分级分离.按照DOM在不同树脂上的吸附特性将其分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPI-A)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).考察了二级处理出水中有机组分的组成分布、三卤甲烷生成势、紫外光谱和红外光谱.结果表明,二级处理出水中的主要成分是HPO-A和HPI,两者含量之和达70.8%.HPO-A是加氯消毒时产生三卤甲烷的主要有机组分,其三卤甲烷生成活性(STHMFP)为232.9μg/mg.而HPO-N、TPI-A、TPI-N和HPI的STHMFP介于100～125μg/mg之间.氯化反应后,HPO-A、HPO-N、TPI-A和HPI的紫外-可见吸光度均降低,而TPI-N则相反.并且HPO-A、HPO-N、TPI-A和TPI-N中的O-H、C=C和苯环的含量降低,而C-O的含量升高,还生成了C=O和C-Cl.