制备高纯二氧化氯技术的重大突破

四川大学化学学院与成都川大金钟科技有限公司联合开发成功一种新型还原剂，与氯酸盐在酸性条件下反应，可生产纯度大于95％的二氧化氯，并在500g／h生产高纯二氧化氯发生器上应用成功。     

酸性甲醛改性对花生壳吸附重金属离子的影响

花生壳的酸性甲醛改性对重金属离子的吸附有较大影响.改性过程使花生壳中一些含有羟基、羧基、芳香环、C-O和C-O-C键的混合物被脱除.改性后花生壳的等电点略有升高,而和羧基有关的表面负电荷量则明显降低.混合物的脱除使Pb2 的吸附量明显降低,Cr3 、Cu2 的吸附量改变不大.改性使羧基减少的同时也暴露了新的Cr3 、Cu2 的吸附位点.改性还有利于增加重金属离子在花生壳内孔中的传质速率,从而使吸附达到平衡的时间略有减少.     

ARIMA模型在苏州河总磷预测中的应用

目前苏州河面临潜在的富营养化危机,氮、磷含量较高的污染源是富营养化形成的直接诱因.选择总磷指标为研究对象,介绍运用时间序列分析法对总磷进行ARIMA建模预测,确定ARIMA(11,0,0)即AR(11)为最终模型,用1986～2003年数据对2004和2005年进行预测,结果得出苏州河总磷在未来2年呈波动下降趋势,最终在0.4～0.6 mg/L之间上下波动,但仍高于地面水Ⅴ类标准.模型适用于苏州河总磷的短期预测,完善苏州河富营养化预测管理系统.     

SRT影响MBR污泥体系去除污染物动力学研究

利用Eckenfelder公式得出了MBR系统中不同污泥停留时间底物降解速率和氨氮的去除速率,结果表明在对数增长阶段和减数增长阶段,SRT为17 d时,对有机底物的降解速率和氨氮的去除速率都高于SRT为8、27、37和42 d的污泥系统对两者的去除,说明SRT对MBR污泥系统的活性有较大影响,确定排泥时间应综合考虑污泥活性、污泥产量和膜通量等因素.     

生物法和化学法回收制革污泥中铬的对比研究

研究了嗜酸性硫杆菌(Thiobacillus)生物沥滤法和1:1硫酸化学沥滤法分离回收制革污泥中的铬.比较了嗜酸性硫杆菌生物沥滤法和化学沥滤法回收制革污泥铬过程中pH、氧化还原电位(ORP)、沉降比(SV)以及铬的沥滤率的变化.试验结果表明,pH是影响制革污泥中铬的沥滤率的关键因素.生物沥滤法在使污泥pH大幅度降低的同时,能很好地改善污泥的沉降性能,对铬的沥滤效果好于化学沥滤法.     

机油高效降解菌群筛选及降解效果初探

从多处受石油污染的土壤中经过初步筛选、混合驯化得到以机油为唯一碳源进行生长代谢的混合菌群.利用此混合菌群进行的降解实验结果表明,该菌群对高浓度机油废水具有较强的降解能力,初始含机油约2.0 g/L的人工废水.接种量为0.1%(菌体湿重/培养液体积),经过7 d的降解,机油可降至403 mg/L,降解率达81.4%;对不同浓度机油废水的降解实验结果表明,在静态实验条件下,机油质量浓度在不高于1 000 mg/L(含1 075 mg/L),混合菌群在降解过程中能自行从降解产酸的不良环境中恢复,机油质量浓度在2 000 mg/L以上,初期产酸较多,pH下降幅度较大,在7 d的周期内,废水pH无法恢复,说明在降解后期仍有大量有机酸积累而未被彻底降解;与葡萄糖共基质的降解实验结果表明,经过7 d的降解.不超过150 mg/L,的葡萄糖与1 000 mg/L机油组成的共基质体系中,机油降解基本不受葡萄糖加入的影响,但可加强早期的降解速率.而葡萄糖高于150 mg/L时,则会对混合菌群的除油率产生抑制,抑制程度随着葡萄糖浓度的提高而加大.     

《太湖流域管理条例》11月实施

我国第一部流域综合性行政法规——《太湖流域管理条例》(以下简称《条例》)近日获得国务院通过,自2011年11月1日起施行。水利部、环境保护部、国务院法制办公室于10月9日就此联合召开新闻发布     

确定大气环境标准方法的探讨

对使用或生产我国尚无环境控制标准污染物质的企业如何管理．经对有关法规、资料的研究，推荐采用确定环境控制标准的方法，以控制这些污染物质的排放及其对环境的影响。     

九寨沟公路和栈道降雨径流污染负荷过程的研究

对九寨沟国家公园中的公路和游客栈道进行了人工降雨试验的设计、操作和测试数据分析.模拟试验选择6处公路和栈道试验区,采用人工降雨方法模拟雨量出现概率60%、历时30 min的降雨.试验按3 min间隔对各试验场降雨径流带出的总磷负荷进行现场监测.研究结果提供了在具有代表性的降雨条件对总磷营养物输出的定量估计.尤其对公路和栈道降雨径流特征获得了认识:污染物初始冲刷浓度期延续约3 min;在降雨强度不变的情况下,污染物负荷率接近常量.大部分污染物负荷可由出现频率较大的小降雨事件输出.表明研究结果提供了一种思路,即可采用平均负荷方式取代过去的平均浓度方式去构建公路和栈道的负荷模型.     

六种“药茶”配方

(1)明目茶:冬桑叶、野菊花,可疏散风热、平肝明目,用于结膜炎。(2)活血茶:红花、檀香,可活血化瘀止痛,用于冠心病、心胶痛。(3)降压茶:菊花、槐花、草决明,可平肝降压、软化血管,用于高血压病、动脉硬化、高血脂症。(4)清暑茶:藿香、佩兰叶、茶叶,可清暑化湿,用于中暑轻症。     

Occurrence and treatment of arsenic in groundwater and soil in northern Mexico and southwestern USA

This review focuses on the occurrence and treatment of arsenic (As) in the arid region of northern Mexico (states of Chihuahua and Coahuila) and bordering states of the southwestern US (New Mexico, Arizona, and Texas), an area known for having high As concentrations. Information assembled and assessed includes the content and probable source of As in water, soil, and sediments and treatment methods that have been applied in the area. High As concentrations were found mainly in groundwater, their source being mostly from natural origin related to volcanic processes with significant anthropogenic contributions near mining and smelting of ores containing arsenic. The affinity of As for solid phases in alkaline conditions common to arid areas precludes it from being present in surface waters, accumulating instead in sediments and shifting its threat to its potential remobilization in reservoir sediments and irrigation waterways. Factors such as oxidation and pH that affect the mobility of As in the subsurface environment are mentioned. Independent of socio-demographic variables, nutritional status, and levels of blood lead, cognitive development in children is being affected when exposed to As. Treatments known to effectively reduce As content to safe drinking water levels as well as those that are capable of reducing As content in soils are discussed. Besides conventional methods, emergent technologies, such as phytoremediation, offer a viable solution to As contamination in drinking water.     

Accumulation in and effects of lead and cadmium on waterfowl and passerines in northern Idaho

Waterfowl and passerines in northern Idaho in 1987 had high levels of lead in their blood and tissues that originated primarily from mining and smelting activities. Four Canada geese (Branta canadensis) and one common goldeneye (Bucephala clangula) found dead contained 8 to 38 microg/g (wet mass) of lead in their livers. These levels exceed the lower lethal limit of 5 microg/g in experimental birds. Two of the Canada geese (one each from the contaminated and reference areas) died with ingested lead shotgun pellets (shot) in their gizzards, whereas the other three birds from the contaminated area contained no ingested shot and evidently died from ingesting environmental lead in sediment or biota. Lead burdens in most American robins (Turdus migratorius) and mallards (Anas platyrhynchos) were high, whereas those in tree swallows (Tachycineta bicolor) were slightly elevated. Lead accumulated to potentially hazardous levels in blood and tissues of some nestling robins (maxima of 0.87 microg/g in blood and 5.6 microg/g in liver) and mallards (maxima of 10.2 microg/g in blood and 2.8 microg/g in liver). In mallards, lead levels and associated physiological characteristics of blood were significantly different in juveniles (HY) versus adults (AHY). Activity of delta-aminolevulinic acid dehydratase (ALAD) was about 87 to 95% lower than values for control birds in experimental studies. Activity of ALAD was significantly inversely correlated with blood lead levels. Cadmium was detected in kidneys of most birds, but even the maximum concentration of 7.5 microg/g in an AHY mallard was below known harmful levels.     

Photodegradation of polychlorinated dibenzo-p-dioxins and dibenzofurans in aqueous solutions and in organic solvents

Aqueous solutions of selected polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were prepared using a generator column and exposed to UV (300 nm) light in the laboratory and to sunlight in an outdoor environment. In the laboratory, additional exposures were also carried out using 60% acetonitrile/water solutions. At 300 nm di- and tetra PCDDs had higher first-order photodegradation rate constants in 60% acetonitrile/water than in pure water. The solvent effect was reversed for PCDFs. These results may be a reflection of the higher polarity of PCDFs compared to PCDDs. In both the indoor and outdoor exposures photodegradation rates decreased with increasing concentrations of chlorination. However, OCDF exposed to 300 nm light in 60% acetonitrile/water and to sunlight in pure water photodegraded more rapidly than tetra CDF. Photolysis rates in sunlight were considerably slower (t(1/2) of 6.4-23 h) than photolysis rates at 300 nm in the laboratory (t(1/2) of 4.3-680 min), reflecting the lower intensity of sunlight in the 300 nm region of the UV/Vis spectrum. The extent of dechlorination of the PCDDs/PCDFs was less than 20% and reductive dechlorination does not appear to be a major process in the photodegradation of PCDDs/PCDFs in aqueous solutions.     

Sorption and degradation of imidacloprid in soil and water

Imidacloprid, the major component of many widely used insecticide formulations, is highly persistent in soils. In this study, the sorption of imidacloprid by six soils as well as its photodegradation and hydrolysis in water were studied. The soils differed significantly in organic matter content and other physical and chemical properties. Sorption increased with increasing soil organic matter content but was not significantly correlated with other soil properties. Removal of organic matter via H2O2 oxidation decreased the sorption. By normalizing the Freundlich coefficients (Kf) to organic matter contents, the variability in obtained sorption coefficient (Kom) was substantially reduced. These results indicate that soil organic matter was the primary sorptive medium for imidacloprid. The low heat of sorption calculated from Kom suggests that partition into soil organic matter was most likely the mechanism. The photodegradation and hydrolysis of imidacloprid in water followed pseudo-first-order kinetics; however, the latter process needed a six-time-higher activation energy. While both processes produced the same main intermediate, they occurred via different pathways. The hydrolysis of imidacloprid was not catalyzed by the high interlayer pH in the presence of metal-saturated clays, which appeared to result from the lack of the pesticide adsorption in the interlayers of clays.     

Kinetics of aerobic and anaerobic biomineralization of atrazine in surface and subsurface agricultural soils in Ohio

The purpose of this study was to assess atrazine mineralization in surface and subsurface samples retrieved from vertical cores of agricultural soils from two farm sites in Ohio. The Defiance site (NW-Ohio) was on soybean-corn rotation and Piketon (S-Ohio) was on continuous corn cultivation. Both sites had a history of atrazine application for at least a couple of decades. The clay fraction increased at the Defiance site and the organic matter and total N content decreased with depth at both sites. Mineralization of atrazine was assessed by measurement of ¹⁴CO₂ during incubation of soil samples with [U-ring-¹⁴C]-atrazine. Abiotic mineralization was negligible in all soil samples. Aerobic mineralization rate constants declined and the corresponding half-lives increased with depth at the Defiance site. Anaerobic mineralization (supplemented with nitrate) was mostly below the detection at the Defiance site. In Piketon samples, the kinetic parameters of aerobic and anaerobic biomineralization of atrazine displayed considerable scatter among replicate cores and duplicate biometers. In general, this study concludes that data especially for anaerobic biomineralization of atrazine can be more variable as compared to aerobic conditions and cannot be extrapolated from one agricultural site to another.     

武汉市秋、冬季大气PM_(2.5)中水溶性离子污染特征及来源分析

采用离子色谱法测定武汉市秋、冬季大气PM2.5中水溶性离子浓度,对其化学组成、质量浓度变化特征及源解析等方面进行了研究。结果表明,NO-3、SO2-4、NH+4为武汉市秋、冬季大气PM2.5中主要的水溶性离子,相关性分析表明,燃烧源是秋、冬季大气PM2.5中水溶性离子的共同来源。成分分析表明,工业区的水溶性离子主要来源于燃烧源,交通区的水溶性离子主要来源于二次污染源,其中包括垃圾焚烧源,植物园的水溶性离子主要来源于二次污染源。     

Concentrations and fluxes of tin in aerosols and rain

The concentration of tin in atmospheric aerosols has been measured at land and ship based sites in the northern and southern hemispheres. Tin concentrations in the northern hemisphere are up to three orders of magnitude greater than those in the southern hemisphere, indicating the importance of anthropogenic inputs to the atmospheric tin cycle. In aerosols sampled in Tallahassee, Florida, tin is correlated with soot carbon in air masses originating in the central U.S., but is not correlated with locally produced soot carbon. Rainwaters collected in Tallahassee, Florida have been analyzed for dissolved tin and major ions. Factor analysis of the results indicates a continental and pollution source for tin. The dissolved fraction of tin in rain represents only a minor component of the deposition flux of tin. Rates of deposition of atmospheric tin are consistent with estimated fluxes of tin to the atmosphere.     

Occurrence and profiles of organic sun-blocking agents in surface waters and sediments in Japanese rivers and lakes

Sun-blocking agents including eight UV filters (UVF) and 10 UV light stabilizers (UVLS) were measured in water and sediment collected from 22 rivers, four sewage treatment plant effluents (STPE) and three lakes in Japan. Total sun blocking agents levels ranged from N.D. to 4928 ng/L and from 2.0 to 3422 μg/kg dry wt in surface water and in sediment, respectively. Benzyl salicylate, benzophenone-3, 2-ethyl hexyl-4-methoxycinnamte (EHMC) and octyl salicylate were dominant in surface water receiving wastewater effluents and STPE, although UV-328, benzophenone and EHMC were dominant in other surface water except background sites. Three UVF and nine UVLS were observed from all sediment and their compositions showed similar patterns with UV-328 and UV-234 as the most prevalent compounds. Homosalate, octocrylene, UV-326, UV-327, UV-328 and UV-234 were significantly correlated with Galaxolide^® in sediments. Concentrations of UV-327 and UV-328 also had strong correlation between those of UV-326 in sediment.     

Measurements and analyses of nitrogen oxides and ozone in the yard and on the roof of a street-canyon in Suzhou

The concentrations of air pollutants such as nitrogen oxides and ozone characterised by very fast chemical reactions can significantly vary within urban street-canyon due to the short distances between sources and receptor. With the primary objective to analyse this issue, NO, NO₂, NO_x, O₃, BTX, and wind flow field were continuously measured for 1 week at two heights (a street-level yard and a 25-m-high rooftop) in an urban canyon in Suzhou (China). The yard ozone concentrations were found to be up to six times lower than on the roof. Different frequency distributions (FD), dynamical and chemical processes of the pollutant variations from yard to roof are discussed to explain the findings. The predominant factors for the dissimilar pollutant vertical diffusion at the two measurement locations were associated to dissimilar fluid-dynamic and heterogeneous removal effects that likely induced dissimilar ozone chemical processes relative to NO_x and BTX precursors.