试析秦皇岛市汤河带状公园二期工程——红飘带设计的生态理念

红飘带位于秦皇岛市的汤河公园,它在将具有视觉冲击的设计元素溶于一体的同时还有着重要的生态目标,提供了一种保护河岸和生态恢复的有效途径.红飘带设计中体现了保护当地生境、最少干预和简约生态设计等生态理念,这些生态理念的应用使得红飘带在一个简洁和经济的设计中将生态与艺术完美结合,成为现在"资源节约型和环境友好型"园林的典范.由此,本文提出应该在整体上进一步提高汤河生态系统健康水平的建议.     

戊唑醇在环境中的降解迁移和生物富集性研究

戊唑醇属于内吸性三唑类杀菌农药,在国内广泛用于田间病虫防治,故其在环境中的归趋备受关注。采用室内模拟试验方法,研究了戊唑醇在水-沉积物中的降解特性、土壤中的吸附性和在斑马鱼中的生物富集性。结果表明:好氧条件下,戊唑醇在河流与湖泊水-沉积物系统中农药总量的降解半衰期分别为533.2、433.2 d;厌氧条件下,河流与湖泊水-沉积物系统中降解半衰期分别为364.8、1 732.9 d;沉积物系统降解半衰期较长,降解速率主要受水中戊唑醇的降解速率影响。戊唑醇在江西红壤、太湖水稻土、常熟乌杉土、东北黑土中的吸附性符合Freundlich方程,Kd值分别为7.4、11.8、11.2和15;吸附性大小次序为东北黑土太湖水稻土常熟乌杉土江西红壤;以有机碳含量表示的土壤吸附常数KOC在698.9~1 635.5之间;影响戊唑醇土壤吸附性的主要因素为土壤有机质含量和p H。戊唑醇在斑马鱼中的生物富集系数BCF8 d为21.52~25.30,具有中等富集性。戊唑醇在水体环境中具有较强稳定性,不易被土壤吸附,且具有一定的生物富集性,可能会对水体和水体生物造成一定的污染。     

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%。     

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。     

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 %.     

石油污染土壤中孤东原油及其馏分的微生物降解性能

分别以孤东油区石油污染土壤中的原油、柴油馏分(180～360℃)、蜡油馏分(360 ～ 500℃)为研究对象,采用BC-Ⅰ和BC-E 2种菌剂,对其进行微生物降解.研究表明,BC-Ⅰ和BC-E菌剂对石油污染土壤中石油烃的降解效果明显,BC-E菌剂对孤东油区石油污染土壤中石油烃的降解率达35.7％.2种菌剂对石油烃中轻馏分的降解效率均远远高于其对重馏分的降解效率.柴油馏分降解产物中鉴定出O1、O2、N1等多种分子类型,其中O2相对丰度远高于O1、N1类型,研究表明,该类化合物是脂肪酸,油样中脂肪酸存在明显的C16、C18优势,降解后低碳数脂肪酸相对丰度略有增加.蜡油(VGO)降解后以m/z=293(C19双环环烷酸)为中心正态分布,烷基咔唑中C5-咔唑丰度最高,苯并咔唑相对丰度很低.O2类化合物丰度很低,表明脂肪酸含量很低,DBE为4或5的O2类化合物明显占优势,对应3～4环环烷酸丰度较高.     

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%。     

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.