高藻水中新生态三价铁混凝行为及其对絮体生长的影响

通过阐释新生态三价铁活性高的机制从而提出混凝剂的连续投加方式对混凝除藻效果的促进作用。与高锰酸钾-铁混凝过程相比,高锰酸钾-亚铁混凝过程初期絮体粒径较小;但经过一段时间后,后者絮体粒径将明显大于前者。Mn(VII)投量为1.7μmol/L时,混凝进行到720 s之前高锰酸钾-亚铁混凝过程中絮体粒径均低于200μm,反应进行到990s时絮体粒径稳步增大到239μm。形成对比的是,高锰酸钾-铁混凝过程进行到720 s和990 s时絮体粒径分别为198μm和204μm。在混凝过程中,亚铁逐步转化生成新生态三价铁,相当于向系统中持续投加混凝剂。在混凝剂总量相同(197.4μmol/L)的情况下,分次连续投加Fe(III)比一次性投加Fe(III)所生成的絮体粒径要大32%。     

Cu-SBA-15催化湿式过氧化氢氧化水溶液中罗丹明B

采用水热晶化法合成了不同含铜量的Cu-SBA-15介孔分子筛,并且用XRD、N2吸附、TEM以及UV-vis对所合成的样品进行表征。以Cu-SBA-15为催化剂,H2O2为氧化剂,催化湿式过氧化水溶液中的罗丹明B,主要考察H2O2浓度、催化剂用量、处理温度、初始pH等因素对罗丹明B氧化效果的影响。结果表明,在同样的处理条件下罗丹明的脱色率明显高于TOC去除率,处理温度、初始pH对罗丹明B的脱色与氧化有重要影响。在罗丹明B初始浓度100 mg/L,H2O2初始浓度1.8 g/L,催化剂量0.3 g/L,温度60℃,pH为7.0,处理时间100 min时,罗丹明B的脱色率为98.6%,TOC去除率为62.8%。     

活性污泥法处理高钙废水中污泥特性的变化

通过单级SBR法处理模拟高钙废水,研究了活性污泥法处理高钙废水的过程中钙离子对COD,MLVSS,MLSS,SVI,污泥增长速率,污泥形态结构及生物相的影响,揭示活性污泥法处理高钙废水的过程中污泥量巨大的原因。采用逐步增加钙离子浓度的方法,检测到在污泥培养期([Ca2+]=0 mg/L),COD去除率为98.1%,MLVSS和MLSS稳定在4 900~5 500mg/L,污泥增长速率为67 mg/(L·d),SVI为55~60 mL/g;在驯化处理期([Ca2+]=120~2 400 mg/L),COD去除率降至87.37%,MLVSS降至2 500 mg/L,MLSS增加至19 300 mg/L,污泥增长速率为212.31 mg/(L·d),SVI降至25 mL/g;在冲击期([Ca2+]=4 000 mg/L),COD去除率降至69.23%,MLVSS降至1 600 mg/L,MLSS迅速增加至24 200 mg/L,污泥增长速率为816.67 mg/(L·d),SVI降至14 mL/g。经显微镜观察发现,污泥絮体由松散变得密实,生物相由钟虫等指示性微生物变为不适应环境的胞囊结构。结果表明,随Ca2+浓度的增加,COD去除率下降,MLSS迅速增加,MLVSS和SVI急剧缩小,说明活性污泥中的活性微生物逐渐减少,而无机物组分逐渐增多;钙离子的加入促使系统碳酸平衡向右移动,使离子状态的钙大部分转化为难降解的碳酸盐,并附着于污泥絮体上,污泥绒粒被压缩,使污泥颗粒密实度及MLSS迅速增加,导致污泥排放量巨大。     

The linear accumulation of atmospheric mercury by vegetable and grass leaves: Potential biomonitors for atmospheric mercury pollution

One question in the use of plants as biomonitors for atmospheric mercury (Hg) is to confirm the linear relationships of Hg concentrations between air and leaves. To explore the origin of Hg in the vegetable and grass leaves, open top chambers (OTCs) experiment was conducted to study the relationships of Hg concentrations between air and leaves of lettuce (Lactuca sativa L.), radish (Raphanus sativus L.), alfalfa (Medicago sativa L.) and ryegrass (Lolium perenne L.). The influence of Hg in soil on Hg accumulation in leaves was studied simultaneously by soil Hg-enriched experiment. Hg concentrations in grass and vegetable leaves and roots were measured in both experiments. Results from OTCs experiment showed that Hg concentrations in leaves of the four species were significantly positively correlated with those in air during the growth time (p?<?0.05), while results from soil Hg-enriched experiment indicated that soil-borne Hg had significant influence on Hg accumulation in the roots of each plant (p?<?0.05), and some influence on vegetable leaves (p?<?0.05), but no significant influence on Hg accumulation in grass leaves (p?>?0.05). Thus, Hg in grass leaves is mainly originated from the atmosphere, and grass leaves are more suitable as potential biomonitors for atmospheric Hg pollution. The effect detection limits (EDLs) for the leaves of alfalfa and ryegrass were 15.1 and 22.2 ng g^–1, respectively, and the biological detection limit (BDL) for alfalfa and ryegrass was 3.4 ng m^–3.     

Effects of soil properties on heavy metal accumulation in flowering Chinese cabbage (Brassica campestris L. ssp. chinensis var. utilis Tsen et Lee) in Pearl River Delta,China

This study was conducted to investigate the effects of soil properties on the heavy metal accumulation in flowering Chinese cabbage (Brassica campestris L. ssp. chinensis var. utilis Tsen et Lee) at the field scale. The concentrations of cadmium (Cd), mercury (Hg), and chromium (Cr) in topsoil and vegetable samples from Nanhai district of Foshan city in the Pearl River Delta (PRD) were analyzed. The results showed that 56.5% of the soil samples exceeded the grade II of the Chinese Soil Environmental Quality Standard (GB 15618-1995) for Hg concentrations, while 8.70% and 17.4% of the vegetable samples exceeded the criteria of the Chinese Safety Qualification of Agricultural Products (GB 18406.1-2001) for Cd and Hg concentrations, respectively. The calculated bio-concentration factor (BCF; i.e., the ratio of the metal concentration in the edible parts of flowering Chinese cabbage to that in soil) values were ranked as: Cd (0.1415) > Cr (0.0061) > Hg (0.0012) (p < 0.01), which demonstrated that Cd was easier to be accumulated in the edible parts of flowering Chinese cabbage than Hg and Cr. Furthermore, the following relationships between (bio-concentration factor) BCF values (BCFs) and soil physicochemical properties were concluded from our results: i) the mean BCFs of coarse-textured soils were higher than those of fine-textured soils; ii) the BCFs decreased with increasing soil pH; iii) the soils with high organic matter(OM) and Cation exchange capacity (CEC) have low BCFs, resulting from their high sorption capacities for Cd, Hg, and Cr. The stepwise linear multiple regression analyses showed that total metal concentrations and available calcium in soils were two main factors controlling the accumulation of Cd, Hg, and Cr in the flowering Chinese cabbage.     

Water–gas exchange of organochlorine pesticides at Lake Chaohu, a large Chinese lake

Organochlorine pesticides (OCPs), a potential threat to ecosystems and human health, are still widely residual in the environment. The residual levels of OCPs in the water and gas phase were monitored in Lake Chaohu, a large Chinese lake, from March 2010 to February 2011. Nineteen types of OCPs were detected in the water with a total concentration of 7.27?±?3.32 ng/l. Aldrin, DDTs and HCHs were the major OCPs in the water, accounting for 38.3 %, 28.9 % and 23.6 % of the total, respectively. The highest mean concentration (12.32 ng/l) in the water was found in September, while the lowest (1.74 ng/l) was found in November. Twenty types of gaseous OCPs were detected in the atmosphere with a total concentration of 542.0?±?636.5 pg/m³. Endosulfan, DDTs and chlordane were the major gaseous OCPs in the atmosphere, accounting for 48.9 %, 22.5 % and 14.4 % of the total, respectively. The mean concentration of gaseous OCPs was significantly higher in summer than in winter. o,p′-DDE was the main metabolite of DDT in both the water and gas phase. Of the HCHs, 52.3 % existed as β-HCH in the water, while α-HCH (37.9 %) and γ-HCH (30.9 %) were dominant isomers in the gas phase. The average fluxes were ?21.11, ?3.30, ?152.41, ?35.50 and ?1314.15 ng/(m²?day) for α-HCH, γ-HCH, HCB, DDT and DDE, respectively. The water–gas exchanges of the five types of OCPs indicate that water was the main potential source of gaseous OCPs in the atmosphere. A sensitivity analysis indicated that the water-gas flux of α-HCH, γ-HCH and DDT is more vulnerable than that of HCB and DDE to the variation of the parameters. The possible source of the HCHs in the water was from the historical usage of lindane; however, that in the air was mainly from the recent usage of lindane. The technical DDT and dicofol might be the source of DDTs in the water and air.     

温度对哑硝化及氧化哑氮释放的影响

采用批次实验的方法探讨了3种不同温度（15℃,25℃,35℃）对亚硝化及其过程中温室气体氧化亚氮释放情况。结果表明,温度对亚硝化过程及氧化亚氮的释放有显著影响。在15～35℃范围内,随着温度的升高,氨氧化率和亚硝化积累率逐渐升高,N2O释放量也逐渐增大,35℃可以作为适宜的亚硝化温度,平均氨氧化率为50．9％,亚硝化积累率为55．6％,NO-2-N与Nrl4-N出水浓度比为1．1,氨氧化率,亚硝化积累率和出水中亚硝氮与氨氮浓度比较合适,从而可以为厌氧氨氧化工艺提供合适的进水,但在此温度下平均N2O释放量相对较高,为1．494la,g／gMLSS。     

Comparison of Analytical Techniques for Measuring Hydrocarbon Emissions from the Manufacture of Fiberglass-Reinforced Plastics

ABSTRACT

Research Triangle Institute and the U.S. Environmental Protection Agency conducted several projects to measure hydrocarbon emissions associated with the manufacture of fiberglass-reinforced plastics. The purpose of these projects was to evaluate pollution prevention techniques to reduce emissions by altering raw materials, application equipment, and operator technique. Analytical techniques were developed to reduce the cost of these emission measurements. Emissions from a small test mold in a temporary total enclosure (TTE) correlated with emissions from full-size production molds in a separate TTE. Gravimetric mass balance measurements inside the TTE generally agreed to within ± 30 % with total hydrocarbon (THC) measurements in the TTE exhaust duct. Pure styrene evaporation tests served as quality control checks for THC measurements and generally agreed to within ± 5 %.     

K-Ca-Mg-Cl-H_2O体系中硫酸钙结晶介稳区的研究

对K-Ca-Mg-Cl-H2O体系中硫酸钙结晶介稳区进行了研究。以一定浓度氯化钙溶液与硫酸镁溶液反应结晶的方式,采用激光散射法测定了不同浓度复合盐溶液和温度下硫酸钙过饱和度与结晶之间的关系,并测定了与之平衡的溶解度,从而确定该体系中硫酸钙结晶介稳区宽度,探讨了影响结晶介稳区的因素,以及硫酸钙结晶和结晶相与复合盐溶液浓度、温度、结晶介稳区之间的关系。     

控制DO及FA条件下短程硝化过程系统稳定性研究

采用SBR工艺以水产品加工废水为研究对象,同时控制进水游离氨（FA）为0．96～1．25mg!L,溶解氧（DO）为1～2mg／L,实现了稳定的短程硝化过程。在此条件下,亚硝化率及氨氮去除率分别大于95％和88％,有机物（COD）去除率在90％以上,亚硝化速率维持在0．9666×10^-3-1．0375×10^-3mgNO2-N／（mgMLSS·h）之间。研究结果表明,同时控制DO及FA在适当范围之内可以获得稳定的短程硝化过程,并可降低系统能耗。本实验采用较低的FA浓度与较高的DO浓度（与OLAND工艺比较）得到了稳定的短程硝化过程,对水产品加工废水处理具有重要应用价值。