长江口海域悬浮颗粒物中钴、镍、铁、锰的化学形态及分布特征研究

研究了重金属Co、Ni、Fe、Mn在长江口及邻近海域悬浮颗粒中的含量、存在形态以及它们在河水与海水混合过程中迁移转化特征,其变化动态特征表明,Co、Ni、Fe以残渣态为主要存在形式;由于Fe-Mn氧化物的形成和吸附作用,使上述金属从水体经过悬浮颗粒转到沉积物中;以Fe-Mn氧化物和碳酸盐形态存在的重金属含量受水体环境的pH和盐度制约。用多元回归分析求得不同形态重金属含量与盐度、pH值和悬浮物含量的变化方程,以及与环境要素间的相互关系。     

Phosphorus fractionation and bio-availability in Taihu Lake(China) sediments

Introduction Sediment phosphorus has been recognized as the mostcritical nutrient limiting lake productivity (OECD, 1982).The concentration of phosphorus in the sediment is often1000 fold higher than that in lake water and its release…     

Zr、Hf在水合氧化铁上的吸附实验研究

制备了两种不同n(Zr)／n(Hf)的Zr、Hf混合溶液,测定了实时生成的水合氧化铁和预先生成的水合氧化铁在不同pH条件下对Zr、Hf的吸附量,并对其吸附等温线进行了研究。研究结果表明:等价元素Zr、Hf在HFO上的吸附是非线性的,在吸附过程中二者发生了分异,Zr的吸附能力要大于Hf;在天然水体pH值范围内(pH≥6),Zr、Hf的吸附量Q及n(Zr)／n(Hf)不随pH发生变化,显示了Zr、Hf相对惰性的行为;Zr、Hf在吸附过程中表现出惊人的一致性行为,Zr、Hf数据间的相关系数R2在0.98以上;Zr、Hf在HFO上的吸附可能是表面羟基与Zr、Hf表面络合反应的结果,并且络合能力Zr>Hf。     

Carbon and hydrogen isotope effects during sorption of organic contaminants on carbonaceous materials

Stable carbon and hydrogen isotopes can be an efficient means to validate biodegradation of organic contaminants in groundwater since it results in an isotopic fractionation. A prerequisite in applying this method in the field is the proof that other processes decreasing the contaminant concentration are conservative with respect to isotope effects. In this paper we show for carbon isotopes of halogenated hydrocarbon compounds [trichloroethene (TCE), cis-dichloroethene (c-DCE), vinylchloride (VC)] and carbon and hydrogen isotopes of BTEX compounds (benzene, toluene, p-xylene) that no significant fractionation occurs during equilibrium sorption onto activated carbon, lignite coke and lignite. In general, effects were in the range of the reproducibility limit of the analytical instrument (0.5 per thousand for delta13C, and 8 per thousand for delta2H). This observation was made for fractions sorbed of less than 5% to more than 95%. Also for rate-limited sorption of TCE onto activated carbon, no significant fractionation in carbon isotopes could be observed. These findings support the assumption that for these classes of compounds, sorption processes in aquifer systems are conservative with respect to isotope effects.     

利用强化混凝去除水源水中天然有机物的研究进展

总结了近年来利用强化混凝去除水源水中天然有机物的研究,重点讨论了其作用机理和主要影响因素.水源水中天然有机物的含量和成分会因水源地和时间的不同而存在差异,对水源水中天然有机物的了解是保证强化混凝效果的基本前提.不同混凝条件下,强化混凝的主导作用机理不同.铁盐混凝剂、较低pH值、较高混凝剂投量和阳离子有利于提高强化混凝的效果.     

黄河兰州段悬浮颗粒物对菲的吸附行为研究

用黄河兰州段水体天然颗粒、人工贫有机质颗粒、伊利石、高岭土、针铁矿作为模拟悬浮颗粒物,采用批量平衡法研究了菲在不同成分颗粒物上的吸附行为,探讨了黄河中上游水体悬浮颗粒物的各种成分对疏水性有机污染物吸附的能力与机理。研究认为,菲在天然颗粒物及粘土矿物颗粒表面的吸附等温线为“S”形,能较好地符合Freundlich方程。粒径相同的不同类型颗粒物对菲的吸附能力大小依次为:粘土矿物>人工贫有机质颗粒>针铁矿>天然颗粒物。对于低有机质含量的兰州黄河颗粒物而言,NOM对菲吸附的贡献较低;溶剂化作用可被用来解释菲在天然颗粒及粘土颗粒表面的吸附行为。     

碳酸盐岩矿区河流沉积物中重金属的形态特征及潜在生态风险

黔西北土法炼锌及铅锌选矿厂对河流造成严重的重金属污染。河流沉积物中重金属的化学形态研究表明,同一采样点中不同重金属的形态分布和同一重金属在不同采样点中的形态分布均有较大差异。这可能与沉积物组分的不同亲和力,不同河段沉积物中粘土矿物、有机质、Fe Mn氧化物含量的不同以及人为活动(生活污水、选矿剂、矿渣等)的加入等有关,而碳酸盐岩地质背景的河床本身可能也有较大影响。潜在生态危害指数法研究表明,沉积物中重金属表现出强生态风险性,产生生态危害的主要重金属污染物是Pb,其后依次是Cd、Cu和Zn。     

几种有机、无机钝化剂对铜污染土壤的钝化效果研究

利用石灰、棉花秆生物炭、玉米秆生物炭和阴离子聚丙烯酰胺作为钝化剂,对3种浓度梯度的铜污染土壤进行处理。采用Tessier形态分级试验对钝化能力和效果进行评价,并以此研究土壤中铜的形态变化。结果发现,石灰(0.2%)、棉花秆生物炭(1%)和玉米秆生物炭(1%)和阴离子聚丙烯酰胺2‰对Cu污染土壤治理均具有较为良好的效果。在铜浓度为50 mg/kg的试验组中,石灰、棉花秆生物炭、玉米杆生物炭和阴离子聚丙烯酰胺可分别将有效态铜含量降低为6.73%、7.92%、8.16%、8.83%。Tessier形态分级试验结果表明:1)随着时间延长,水溶态+交换态铜含量自然降低;2)加入钝化剂的试验组,有效态Cu含量明显降低,缓和态和无毒态的Cu含量有不同程度地增加。说明施用钝化剂促进Cu由有效态向缓和态和无毒态转化是土壤原位修复的重要机制。     

改良剂对土壤Sb赋存形态和生物可给性的影响

采用室内土壤培养法研究不同改良剂(骨炭、生物调理剂、沸石、石灰、油菜秸秆、生物炭、堆肥和赤泥)对土壤Sb化学形态转化和生物可给性的影响.结果表明,除堆肥处理外,添加5%的其他7种改良剂均显著地提高了土壤的p H值,其中石灰处理p H最为明显.BCR分级提取表明,土壤Sb主要以残渣态形式存在.添加生石灰、骨炭和生物调理剂显著地提高了土壤Sb的移动性,而添加赤泥、生物炭和堆肥却显著地降低了土壤Sb的移动性.添加不同的改良剂对土壤Sb的生物可给性也有影响,但是受不同培养时间影响较大.培养2个月后,添加5%的堆肥、5%赤泥和5%生物炭处理导致土壤Sb的生物可给性含量分别比对照降低38%、23%和20%;而添加5%的石灰、5%油菜秸秆和5%的生物调理剂处理导致土壤Sb的生物可给性含量分别比对照提高1.07倍、1.06倍和1.11倍.堆肥、赤泥和生物炭是钝化Sb污染土壤的潜力材料.     

Spectroscopic studies of dye-surfactant interactions with the co-existence of heavy metal ions for foam fractionation

The interaction between a cationic dye Methylene Blue (MB) and an anionic surfactant sodium dodecyl sulfate (SDS) with the presence of Cd²⁺ was investigated spectrophotometrically in a certain concentration range. The spectrophotometric measurements of dye-metal ion-surfactant system were carried out. The results indicated that the SDS concentration had a significant influence on the dye spectrum, while the addition of Cd²⁺ hardly caused change of the maximum value of absorbance. According to this observation, we concluded that electrostatic and hydrophobic interaction between dye and surfactant occurred up to a certain level, and the homo-ions Cd²⁺ almost exerted no effect on the dye-surfactant complexation, establishing a theoretical foundation for simultaneous removal of organic dye and heavy metal using foam fractionation. Meanwhile, the effects of their interaction on foam performance were investigated. The results showed that the addition of Cd²⁺ favored the tendency to ameliorate foam properties just contrary to MB. The feasibility of foam separation for dye and heavy metal removal from simulated wastewater was also confirmed using a continuous foam fractionator. In the simultaneous removal process, with the initial SDS concentration ranging from 0.5 to 5.0 mmol/L, the maximum removal efficiencies of MB and Cd²⁺ were obtained as 99.69% and 99.61%, respectively. The enrichment ratios were reduced from 24.34 to 7.65 for MB and from 22.01 to 3.35 for Cd²⁺.