人工生物浮岛载体的研究进展

为改善浮岛性能,减少有机高分子材料所造成的"白色污染",有必要研制开发新型浮岛载体-轻质高效微生物载体.从国内外浮岛的研究现状看,目前在工程实例中广泛采用的是有机高分子材料载体,无机材料的浮岛尚处于实验研究阶段.在对几种典型无机材料-轻质滤料的物理特性、成分、化学稳定性、价格、来源等方面进行综合分析后可知,用无机材料制作有机浮岛载体的替代品是可行的,具有广阔的发展前景,但还需进一步的研究和探索.     

化学药剂处理湖泊沉积物磷污染的实验研究

试验了氢氧化钙、硫酸铝、硝酸钙、硫酸亚铁对抑制湖泊沉积物向水体释放磷的有效性,药剂投加量分别为1：1、1：2和过量,试验历时24d,4种药剂对水体磷去除率最高分别可达到86．2％、91．7％、90．3％和93．1％,但处理效果随时间会发生变化。     

SAF-化学絮凝-微滤膜组合工艺处理高浓度生活污水的试验研究

采用SAF-化学絮凝-微滤分离膜组合工艺对高浓度生活污水进行处理.SAF处理系统对污染物的去除效果良好,CODCr,BOD5,SS和NH4 -N的去除率分别为92%,93%,90%和98%.SAF生物处理系统的出水再经化学絮凝和微滤分离膜深度处理后,CODCr,BOD5,NH4 -N,PO43--P的浓度分别低于40 mg/L,10mg/L,4mg/L,0.3mg/L;浊度小于0.5NTU,色度小于10度.试验结果表明该组合工艺处理后的污水水质优良,可满足生活杂用和市政杂用.     

受污染地表水体生物修复技术研究进展

主要介绍了受污染地表水体生物修复技术的类型及特点,综述了国内外关于受污染地表水体生物修复技术研究及应用的现状,并对生物修复技术的研究及应用进行了展望.     

可吸入颗粒物产生机理的研究

本文指出可吸入颗粒物产生机理的研究与源解析技术之间既有区别又有联系,对国内外在可吸入颗粒物产生机理方面的研究成果进行了综述,国外对可吸入颗粒物产生机理的研究集中在排放特性的研究、模型的建立、内聚力/分离力的研究和物理-化学特性研究上,国内主要进行了有关可吸入颗粒物基本特性的研究.     

北京市公园土壤铜、铅含量及化学形态分布特征

对北京市的12个公园进行表层、深层土壤样品的重金属Cu、Pb含量分析,并对其中10个公园的表层、深层土壤样品进行Cu、Pb的化学形态分析。研究结果表明:北京市部分公园的深层土壤已在某种程度上受到人为扰动,大多数公园表层土壤中存在着一定的Cu、Pb含量积累现象,总体上市区公园比郊区公园明显。公园表层、深层土壤中Cu形态分布的总体规律均为残渣晶格态>有机结合态>铁锰氧化物结合态>碳酸盐结合态>可交换态,表层、深层土壤中Pb形态分布的总体规律均为残渣晶格态>铁锰氧化物结合态>有机结合态>碳酸盐结合态>可交换态,但表层土壤中活性态Cu、Pb的平均比例较深层土壤均有所上升,部分市区公园表层土壤中Cu、Pb的含量较高且活性态比例较大,具有一定的释放潜力和生物有效性。     

HDTMA改性粘土吸附固定沉积物间隙水中多环芳烃的模拟研究

选用经过十六烷三甲基溴化铵(HDTMA-Br)改性的粘土矿物为吸附剂,探讨其对水中多环芳烃类有机污染物的吸附性能。结果表明,HDTMA改性土吸附固定水中多环芳烃的能力比天然沉积物要高得多且吸附稳定。本文还讨论了环境温度、pH值、盐度、振荡时间、污染物初始浓度以及投土量对吸附性能的影响以确定吸附的适宜条件。根据实验结论,将HDTMA改性土投到实际间隙水样品中,经过充分的吸附,结果显示,经HDTMA改性粘土吸附后的间隙水中多环芳烃的含量均在检出线以下,说明HDTMA改性土可以有效地吸附固定沉积物间隙水中的多环芳烃,降低其迁移性,防止其释放产生二次污染。     

卫星光学反射膜光谱反射率空间综合环境退化研究

对玻璃基底和金属基底的铝反射膜在紫外、低能电子、低能质子的综合环境作用下的光谱反射率退化进行了实验研究。试验结果表明两种铝反射膜的光谱反射率均发生了退化,且光谱反射率的退化主要集中在可见光波段,在近红外波段退化很小;玻璃基底铝反射膜退化在420 nm左右出现峰值点,2种金属基底铝反射膜的退化的峰值点在450 nm左右。由于电荷沉积在玻璃中后会抑制带电粒子入射,因此玻璃基底铝反射膜的退化要小于金属基底铝反射膜。     

Observation of atmospheric nitrous acid with DOAS in Beijing, China

Measurements of nitrous acid （HONO） and nitrogen dioxide （NO2） in Beijing City have been performed by means of a developed differential optical absorption spectroscopy （DOAS） system based on photodiode array （PDA）, during the autumn of 2004. HONO and NO2 were simultaneously identified by their characteristic absorption bands in the spectral region between 337 nm and 372 nm with high sensibility and time resolution. The concentrations of HONO exhibit obviously diurnal variation with a nocturnal maximum and a daytime minimum. The highest HONO value up to 11.8 μg/m^3 was observed during the night of 2/3 September. Possible sources of the observed HONO were discussed. Good correlation to NO2 indicates that NO2 is a main source component. The measurement also shows direct emission of HONO is an imnortant source in strongly polluted urban area.     

Effect of humic substances on the precipitation of calcium phosphate

For phosphorus （P） recovery from wastewater, the effect of humic substances （HS） on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate （as P） and 20 mg/L HS （as dissolved organic carbon, DOC） at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium （Ca） and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction （XRD） and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0, the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite （HAP） by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate.