赭石对模拟重金属废水的吸附效果研究

采用模拟重金属废水的正交试验设计,进行赭石对模拟重金属废水的吸附效果研究,探讨pH、赭石加入量和振荡时间等影响因素对吸附效果的影响。结果表明,在一定pH、赭石加入量和振荡时间条件下,赭石对6种重金属（Pb、Cd、Mn、Zn、Cr和Ni）均有较好吸附效果,对Pb、Cd、Mn、Zn和Cr的最大吸附率可达100%,对Ni的吸附率达8963%。处理后废水中重金属达到污水排放标准。各影响因素对Mn、Zn和Cr吸附效率的影响大小表现为：pH＞赭石加入量＞振荡时间,Ni和Cd表现为：赭石加入量＞pH＞振荡时间,Pb表现为：pH＞振荡时间＞赭石加入量。赭石对废水中重金属吸附的最佳条件为赭石加入量40 g/L,pH 10～10.5,振荡时间2 h。     

利用UVC去除低浓度苯的实验研究

探讨了不同实验参数对苯的UVC去除效果的影响,获得了苯的去除率与苯的初始浓度、气体流量、相对湿度和氧气含量等参数之间的关系。数据表明,在实验条件范围内,苯的去除率的倒数与苯初始浓度、气体流量之间为线性关系;苯的去除率随相对湿度的增加呈现先升高后缓慢降低的关系,最佳相对湿度值在30%～50%之间;苯的去除率随氧气量的增加而缓慢增加;波长为185+254 nm的UV与254 nm的UV相比净化效果更为理想。还分析了苯降解产生的中间产物,探讨了苯的降解机理。     

湖岸缓冲带反硝化作用的研究进展

反硝化作用是湖岸缓冲带去除硝酸盐的重要途径。湖岸缓冲带是联系陆地与湖泊生态系的纽带,不仅为许多动植物提供适宜生境,而且通过反硝化作用能去除地下水中的硝酸盐,提高湖泊水质。概述不同检测反硝化速率的方法,并对比各种方法的优点与缺点。阐述反硝化作用的影响因素：厌氧环境、有机碳、湖岸坡度、缓冲带坡度、pH与温度、硝酸盐浓度。介绍反硝化速率模型的研究开发状况。最后,提出了目前国内外反硝化研究中存在的不足及发展方向。     

固定化假单胞菌降解油烟废气的研究

将从受油烟废气污染严重的土壤中分离筛选的具有较强降解油烟能力的假单胞菌利用活性炭为填料吸附固定后制成填料床生物反应器。实验考察了进气浓度、气体流量、气体停留时间、容积负荷等对油烟去除率的影响,初步研究了生物反应器的抗冲击能力。结果表明,活性炭填料对菌体具有良好的吸附能力,当油烟进气浓度小于100 mg/L,气体流速小于8 L/h,停留时间大于30 s,容积负荷为2.6～18.9 g油烟废气/(m³·h),生物反应器的降解效率可达到95%以上,且活性炭填料床反应器具有较强的抗冲击能力。     

微电解-催化氧化法处理高浓度甲醇废水

采用微电解一催化氧化法处理某化工厂的高浓度甲醇生产废水。实验结果表明：在进水pH为2．0、铁炭质量比为2、微电解时间为14h、空气流量为500mL／min的条件下,废水经微电解处理后,出水COD由原来的约7000mg/L降至约1000mg／L,COD去除率达85％以上;在过滤后微电解出水COD约为950mg／L、微电解出水pH为6．5、空气流量为300mL／min、催化氧化时间为3h时的条件下,经催化氧化处理后,出水COD降至100mg/L以下,出水水质达到GB8978--1996《污水综合排放标准》的二级标准。     

Concentration Effects on Competitive Sorption of Trichloroethylene and Tetrachloroethylene to the Roots of Typha latifolia: Implications for Phytomonitoring

Uptake of organic contaminants by plant roots consists of two consecutive steps: sorption to plant roots and entrance into root xylem tissues through epidermal and endodermic membranes. Most research pertaining to phytoremediation assumed that sorption to plant roots is linear and non-competitive. A growing body of evidence, however, is suggesting that sorption to plant roots is nonlinear and competitive. The objective of this study was to examine the concentration effects of chemical constituents on the competitive sorption of trichloroethylene (TCE) and tetrachloroethylene (PCE) to the roots of Typha latifolia. Competitive sorption was clearly demonstrated by the reduced sorption of TCE and PCE in bi-solute systems than in single-solute systems. Concentration is an important factor affecting the extent of competition. In bi-solute systems, the PCE/TCE ratio on root surface approximately reflected the contaminant footprints in solution. The result was attributed to limited high energetically favorable sorption sites on the root surface and similar sorption mechanisms of TCE and PCE. The results hold significant importance for the application of phytomonitoring of organic contaminant mixtures.     

安全社区建设过程中的科学方法研究

随着安全社区在我国推广工作的不断深入开展,与之相适应的科学方法的运用水平与有效性已经显得相对不足。由于安全社区建设和伤害预防工作涉及社会学、管理学、预防医学、安全科学、心理学等多个学科,其学科跨度及巨大复杂性,使得没有任何一个学科可以单独地应用完成,并且它具有许多不同于其他学科的特殊性,因此,关于安全社区建设过程中的科学方法研究十分必要。     

Ecological risk assessment of open coal mine area

The coal mine areas in China have the serious conflicts between resources exploitation and ecology safety, therefore the coal mine ecological risk assessment is an important problem which relates to the sustainability of coal mines to regions and the whole country. In this study, open coal mine area serves as researching object, heavy metals, soil erosion and coast are screened out as risk resources, soil wireworm as the receiver of heavy metals risk, biotope ecosystem as the receiver of soil erosion and coast risk; ecological indexes are calculated with species background index, biological diversity index and natural degree index, ecological friability indexes are calculated with soil fertility index, plant coverage, plant species diversity index, soil wireworm index and maturity index, and the typical coal mine area assessment indexes system is established. In addition, the regional ecological risk assessment is conducted on the friable ecological system of Fuxin Haizhou open coal mine area. Examples are researched of Haizhou open coal mine, the coal mine risk distribution is established, and foundations are provided for the administrative decision-making.     

Distribution, sources, and potential risk of polycyclic aromatic hydrocarbons (PAHs) in drinking water resources from Henan Province in middle of China

Distribution and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in drinking water resources have been carried out for the first time in Henan Province, China. Water samples collected from four river systems and their tributaries, as well as groundwater resources, were analyzed according to EPA method 525.2. Total of 68 water samples were collected in 18 cities in Henan province in May, August and November, 2001. Concentrations of sum of 16 priority PAHs in water samples ranged from 15 to 844 ng/L with a mean value of 178 +/- 210 ng/L (n = 68). The spatial and temporal distribution of PAHs showed that the Huanghe and the Huaihe river systems had relatively higher concentrations of total PAHs. Higher concentrations of total PAHs were observed in August and November than in May, with respective mean values of 262, 232 and 33.6 ng/L. Ratios of Ant/(Ant + Phe) and Flur/(Flur + Pyr) were calculated to evaluate the possible sources of PAH contamination, which indicated that the coal combustion sources were the main contributors to PAHs in most drinking water resources. Some petrogenic (or pyrolytic) sources of PAHs were also found. The toxic equivalency factors (TEFs) were used to calculate benzo[a]pyrene equivalents (BaPE) for water samples. The average value of BaPE was 0.6 ng/L. The values in most stations were much lower than the guideline values in drinking water of Chinese Environmental Protection Agency (CEPA, 2.8 ng/L) and the US Environmental Protection Agency (US EPA, 200 ng/L). Overall, the drinking water resources in Henan province showed some carcinogenic potential.     

Concentrations and inventories of polycyclic aromatic hydrocarbons and organochlorine pesticides in watershed soils in the Pearl River Delta,China

The concentration levels, source, and inventories of polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) in 55 surface vegetable soils in the watershed of the Pearl River Delta (PRD) were analyzed and compared with those of the surface sediments in the Pearl River Estuary (PRE) and northern South China Sea (SCS). The 16 priority PAHs on US EPA list range from 58 to 3,077 microg/kg (average: 315 microg/kg). The concentrations of DDTs and HCHs range from 3.58 to 831 microg/kg (average: 82.1 microg/kg) and from 0.19 to 42.3 microg/kg (average: 4.42 microg/kg). The ratios of DDT/ (DDD+DDE) are higher than 2 in majority of the soil samples, suggesting that DDT contamination still exists. The PAH ratios suggest that the source of PAHs is petroleum, and combustion of fossil fuel, biomass, and coal. The average concentrations of PAHs and the linear regression slope between PAHs and TOC for the soils and the sediments are quite similar. It was estimated that the soil mass inventories at 0-20 cm depth are 1,292 metric tons for PAHs and 356 metric tons for OCPs in the studied region. The average PAHs inventory per unit area for the soil samples investigated in PRD is about 0.86 time that of surface sediments in the Pearl River Estuary, and about 2.43 times that of surface sediments in the northern South China Sea. PAHs in the soils in PRD have similar source to those of the surface sediments in PRE. All of those may suggest that PAHs in PRE and SCS are probably mainly inputted from the soils in PRD via soil erosion and river transport.