厌氧-Carrousel氧化沟处理亚麻沤制废水的试验研究

亚麻沤制废水是一种高浓度有机废水,经厌氧处理后,出水仍不达标.采用厌氧-Carrousel氧化沟进行后续处理试验,并引进了ACF32微生物制剂进行污泥培养,出水CODCr值在200 mg/L左右,TN值维持在22 mg/L左右,TP值维持在3 mg/L以下,最后讨论了试验中影响处理效果的主要因素.     

SBR处理铁路洗涤废水试验研究

铁路洗涤废水中含有的主要污染物直链烷基苯磺酸钠(LAS)是我国环境标准中第2类污染物质.目前,铁路洗涤废水的处理以物理和化学法为主,存在效果不稳定、成本较高和工艺复杂等问题,急需寻求一种适合铁路洗涤废水特点的处理工艺.用SBR小试装置进行铁路洗涤废水处理实验研究,并且投加LAS降解菌于SBR中,进行了工艺参数的确定,处理效果考察和投菌前后对比等方面的初步研究.     

矿化垃圾混配种植介质的盆栽实验研究

矿化垃圾营养成分和有机质含量较高,但含有重金属和盐分.为了解矿化垃圾的施加比例对植物的生长影响以及植物对矿化垃圾混配种植介质中营养成分的吸收和重金属的富集,将矿化垃圾和本地绿化土按照不同比例混配,研究混配种植介质的理化性质的改善条件、矿化垃圾对植物体内的生物量和叶绿素含量的影响、植物对混配种植介质中营养成分的吸收量以及植物体内各种重金属累积浓度,探索矿化垃圾的最佳施用比例.实验结果表明,矿化垃圾可改善上海本地土壤贫瘠的普遍状况,其添加质量分数在50%～75%合适,对植物生长有利.     

聚硅硫酸铝的形貌结构和絮凝机理

以工业水玻璃、工业硫酸铝为原料制得聚硅硫酸铝(PASS)复合絮凝剂,采用电子显微镜观察了不同,nAl/n(Si)的PASS的形貌,借助倒置式生物显微镜分析了PASS所形成絮体的形貌并用激光粒度分析仪对絮体粒度分布进行了测定,通过红外光谱和X-射线衍射研究了PASS中铝与聚硅酸的相互作用情况,考察了模拟江水中胶体颗粒物和PASS水解物的Zeta电位随pH值的变化,在此基础上探讨分析了PASS的絮凝机理和絮凝过程.结果发现:nAl/n(Si)对PASS的形貌有较大影响,絮体粒度分布的数据印证了该结果;红外光谱图表明PASS中有Si-O-Al振动峰出现,峰强度随nAl/n(Si)减小而增大;X-射线衍射图证实了聚硅硫酸铝不是晶体,而是铝水解产物与聚硅酸共同作用形成的无定型聚合物;吸附架桥及粘结卷裹作用是PASS絮凝时的主导作用.     

面向灾害应用的遥感影像融合统一理论体系设计

由于缺乏统一的理论体系指导,目前遥感影像融合研究相对比较混乱。针对像素级融合统一理论框架的思想,指出了遥感影像融合研究的方向和思路,将像素级融合统一理论框架逐步向特征级和决策级推广,着重发展了一套遥感影像融合统一理论体系。在统一体系下,面向灾害监测应用,按照理论研究、方法研究和应用研究的3个层次进行该理论体系的设计。     

Anaerobic degradation of nonylphenol in soil

This study investigated the effects of various factors on the anaerobic degradation of nonylphenol (NP) in soil. The results show that the optimal pH for NP degradation was 7.0 and that the degradation rate was enhanced when the temperature was increased. The addition of compost enhanced NP degradation. The individual addition of the electron donors lactate, acetate, and pyruvate inhibited NP degradation. The high-to-low order of NP degradation rates under three anaerobic conditions was sulfate-reducing conditions > methanogenic conditions > nitrate-reducing conditions. The results show that sulfate-reducing bacteria, methanogen, and eubacteria are involved in the anaerobic degradation of NP, with sulfate-reducing bacteria being a major component of the soil. Of the anaerobic strains isolated from the soil samples, strain AT3 expressed the best ability to biodegrade NP.     

Temporal change in the distribution patterns of hexachlorobenzene and dichlorodiphenyltrichloroethane among various soil organic matter fractions

Residence time-dependent distribution patterns of hexachlorobenzene (HCB) and dichlorodiphenyltrichloroethane (DDT) among different soil organic matter fractions of three Chinese soils were investigated. Soil organic matter (SOM) was fractionated into fulvic acid (FA), humic acid (HA), bound-humic acid (BHA), lipid, and insoluble residue (IR) fractions using methyl isobutyl ketone (MIBK) method. Results revealed that as the residence time prolonged, the amounts of HCB and DDT in the FA, HA and BHA fractions decreased, while those in the lipid and IR fractions increased. One- and two-compartment first order, and one- and two-parameter pore-diffusion kinetic models were used to describe the mobility of HCB and DDT from the FA, HA and BHA fractions. The results suggest that excellent agreements were achieved between the experimental data and fits to the two-compartment first order kinetic model (R2>0.97). The transfer rates of HCB and DDT followed the order FA>HA>BHA.     

Distribution of elements in needles of Pinus massoniana (Lamb.) was uneven and affected by needle age

Macronutrients (P, S, K, Na, Mg, Ca), heavy metals (Fe, Zn, Mn, Cu, Pb, Cr, Ni, Cd,) and Al concentrations as well as values of Ca/Al in the tip, middle and base sections, and sheaths of current year and previous year needles of Pinus massoniana from Xiqiao Mountain were analyzed and the distribution patterns of those elements were compared. The results indicated that many elements were unevenly distributed among the different components of needles. Possible deficiency of P, K, Ca, Mn and Al toxicity occurred in needles under air pollution. Heavy metals may threaten the health of Masson pine. Needle sheaths were good places to look for particulate pollutants, in this case including Fe, Cu, Zn, Pb, Cr, Cd and Al.     

Heavy metals in bark of <Emphasis Type="Italic">Pinus massoniana</Emphasis> (Lamb.) as an indicator of atmospheric deposition near a smeltery at Qujiang,China

Goal, Scope and Background Rapid urbanization and the expansion of industrial activities in the past several decades have led to large increases in emissions of pollutants in the Pearl River Delta of south China. Recent reports have suggested that industrial emission is a major factor contributing to the damages in current natural ecosystem in the Delta area. Tree barks have been used successfully to monitor the levels of atmospheric metal deposition in many areas, but rarely in China. This study aimed at determining whether atmospheric heavy metal deposition from a Pb-Zn smeltery at Qujiang, Guangdong province, could be accurately reflected both in the inner bark and the outer bark of Masson pine (Pinus massoniana L.). The impact of the emission from smeltery on the soils beneath the trees and the relationships of the concentrations between the soils and the barks were also analyzed. Methods Barks around the bole of Pinus massoniana from a pine forest near a Pb-Zn smeltery at Qujiang and a reference forest at Dinghushan natural reserve were sampled with a stainless knife at an average height of 1.5 m above the ground. Mosses and lichens on the surface barks were cleaned prior to sampling. The samples were carefully divided into the inner bark (living part) and the outer bark (dead part) in the laboratory, and dried and ground, respectively. After being dry-ashed, the powder of the barks was dissolved in HNO₃. The solutions were analyzed for iron (Fe), manganese (Mn), copper (Cu), zinc (Zn), chromium (Cr), nickel (Ni) and cobalt (Co) by inductively coupled plasmas emission spectrometry (ICP, PS-1000AT, USA) and Cadmium (Cd) and lead (Pb) by graphite furnace atomic absorption spectrometry (GFAAS, ZEENIT 60, Germany). Surface soils (0–10 cm) beneath the sample trees were also collected and analyzed for the selected metals. Results and Discussion Concentrations of the selected metals in soils at Qujiang were far above their environmental background values in the area, except for Fe and Mn, whilst at Dinghushan, they were far below their background values, except for Cd and Co. Levels of the metals, in particular Pb and Zn, in the soils beneath the sample trees at Qujiang were higher than those at Dinghushan with statistical significance. The result suggested that the pine forest soils at Qujiang had a great input of heavy metals from wet and dry atmospheric deposition, with the Pb-Zn smeltery most probably being the source. Levels of Cu, Fe, Mn, Zn, Ni and Pb at Qujiang, both in the inner and the outer bark, were statistically higher than those at Dinghushan. Higher concentrations of Pb, Fe, Zn and Cu may come from the stem-flow of elements leached from the canopy, soil splash on the 1.5 m height and sorption of metals in the mosses and lichens growing on the bark, which were direct or indirect results from the atmospheric deposition. Levels of heavy metals in the outer barks were associated well with the metal concentrations in the soil, reflecting the close relationships between the metal atmospheric deposition and their accumulation in the outer bark of Masson pine. The significant (p<0.01) correlations of Fe-Cu, Fe-Cr, Fe-Pb, Fe-Ni, Pb-Ni, and Pb-Zn in the outer barks at Qujiang again suggested a common source for the metals. The correlation only occurred between Pb and Ni, Cd and Co in the outer barks at Dinghushan, which suggested that those metals must possibly have other uncommon sources. Conclusions Atmospheric deposition of the selected metals was great at Qujiang, based on the levels in the bark of Pinus massoniana and on the concentrations in the soils beneath the trees compared with that at Dinghushan. Bark of Pinus massoniana, especially the outer bark, was an indicator of metal loading at least at the time of sampling. Recommendations and Perspectives The results from this study and the techniques employed constituted a new contribution to the development of biogeochemical methods for environmental monitoring particularly in areas with high frequency of pollution in China. The method would be of value for follow up studies aimed at the assessment of industrial pollution in other areas similar with the Pearl River Delta.     

固相萃取-气相色谱法测定水中硝基氯苯类化合物

建立固相萃取-气相色谱法测定水中15种硝基氯苯类化合物的方法。选用HLB柱为固相萃取柱,选用环己烷∶丙酮(3∶1,V∶V)混合溶剂作洗脱剂,得到方法检出限为0.011～0.040μg/L。空白水样加标回收率为73.6%～119%,相对标准偏差为6.1%～13.9%,精密度和准确度良好。对成分不复杂的实际水样进行测定,加标回收率为64.1%～118%,相对标准偏差为5.8%～15.6%,该方法能够基本满足成分不复杂的环境水体中痕量硝基氯苯类化合物的测定。