Effects of SOM, surfactant and pH on the sorption-desorption and mobility of prometryne in soils

Sorption and desorption of the herbicide prometryne in two types of soil subjected to the changes of pH and soil organic matter and surfactant were investigated. The sorption and desorption isotherms were expressed by the Freundlich equation. Freundlich K_f and n values indicate that soil organic matter was the major factor affecting prometryne behavior in the test soils. We also quantified the prometryne sorption and desorption behavior in soils, which arose from the application of Triton X-100 (TX100), a nonionic surfactant and change in pH. Application of TX100 led to a general decrease in prometryne sorption to the soils and an increase in desorption from the soils when applied in dosages of the critical micella concentration (CMC) 0.5, 1 and 2. At the concentration below the CMC, the non-ionic surfactant showed a tendency to decrease prometryne sorption and desorption. It appeared that TX100 dosages above CMC were required to effectively mobilize prometryne. Results indicate that the maximum prometryne sorption and minimum prometryne desorption in soils were achieved when the solution pH was near its pK_a. Finally, the influence of TX100 on the mobility of prometryne in soils using soil thin-layer chromatography was examined.     

Removing and recovering gas-phase elemental mercury by Cu(x)Co(3-x)O(4) (0.75< or = x < or =2.25) in the presence of sulphur compounds

The Hg(0) oxidation ability and reusability of Cu(x)Co(3-x)O(4) were investigated in an attempt to improve SO(2) anti-poisoning ability of metal oxide and produce more economic and effective sorbents for the control of Hg(0) emission from combustion processes. The influence of copper content on Cu(x)Co(3-x)O(4)'s (0.75< or = x < or =2.25) oxidation ability of Hg(0) in the presence of SO(2) was investigated. According to the X-ray diffraction, Brunauer-Emmett-Teller (BET) and mass balance analysis on mercury, we found that Cu(1.5)Co(1.5)O(4) showed the highest S(BET) and best Hg(0) oxidation ability. With continuous increase of x from 0.75 to 2.25, Cu(x)Co(3-x)O(4)'s SO(2) anti-poisoning ability increased. The analysis results of the X-ray photoelectron spectroscopy manifested that the adsorptive mercury species on spent Cu(1.5)Co(1.5)O(4) was HgO. The spent Cu(1.5)Co(1.5)O(4) could be regenerated by thermal decomposition at 673K and regenerated Cu(1.5)Co(1.5)O(4) showed higher Hg(0) oxidation ability due to Hg-doping. Regenerated enrichment Hg(0) was collected using activated carbon at an ambient temperature to eliminate the secondary pollution.     

Cobalt and manganese stress in the microalga Pavlova viridis （Prymnesiophyceae）： Effects on lipid peroxidation and antioxidant enzymes

Pollution of marine environment has become an issue of major concern in recent years.Serious environmental pollution by heavy metals results from their increasing utilization in industrial processes and because most heavy metals are transported into the marine environment and accumulated without decomposition.The aim of the present study is to investigate the effects on growth,pigments, lipid peroxidation,and some antioxidant enzyme activities of marine microalga Pavlova viridis,in response to elevated concentrations of cobalt(Co)and manganese(Mn),especially with regard to the involvement of antioxidative defences against heavy metal-induced oxidative stress.In response to Co~(2 ),lipid peroxidation was enhanced compared to the control,as an indication of the oxidative damage caused by metal concentration assayed in the microalgal cells but not Mn~(2 ).Exposure of Pavlova viridis to the two metals caused changes in enzyme activities in a different manner,depending on the metal assayed:after Co~(2 )treatments,total superoxide dismutase(SOD)activity was irregular,although it was not significantly affected by Mn~(2 )exposure.Co~(2 )and Mn~(2 )stimulated the activities of catalase(CAT)and glutathione(GSH),whereas,ghitathione peroxidase(GPX)showed a remarkable increase in activity in response to Co~(2 )treatments and decreased gradually with Mn~(2 )concentration,up to 50μmol/L,and then rose very rapidly,reaching to about 38.98% at 200μmol/L Mn~(2 ).These results suggest that an activation of some antioxidant enzymes was enhanced,to counteract the oxidative stress induced by the two metals at higher concentration.     

21世纪前期湖南可持续发展的工业化对策研究

湖南是我国中部农业精华地带的组成部分，长期以来，由于受资源禀赋、地理区位、国家政策导向和原有基础等多重影响，形成了传统农业发达而工业发展相对滞后的区域经济。21世纪前期，为实现经济总量的快速增长和区域经济质量的提升，追赶上东部经济发达地区，湖南提出了工业化带动的区域经济战略。由于现阶段国内外经济环境已经发生了较大的变化，加之在科技发展、资源结构和区域经济实力等方面存在与东部沿海发达地区较大的差异，湖南的工业化必须在对原有传统工业化战略有所扬弃的基础上，形成具有自身特色的可持续发展的工业化战略。战略的基本点表现为：(1)将优势传统农业产业进行工业化改造，实现高新技术与传统产业的结合；(2)打破城乡户籍隔离体制，依托城镇化的率先突破，带动工业化发展；(3)高度警觉工业化可能产生的负效应，分类推进，实现不同地区可持续发展的工业化战略。     

高能-钝感复合装药结构冲击波感度数值模拟

为得到复合装药结构对冲击波感度的响应情况,采用显式有限元程序AUTODYN对高能炸药和钝感炸药的复合结构进行隔板试验的数值模拟。分析被发药柱内部的压力时程曲线,并据此判定是否发生爆轰,继而得到反映冲击波感度的隔板值。模拟结果显示复合结构尺寸与冲击波感度的非线性关系,拟合得到的公式可为工程中装药结构设计提供参考依据。这种结构用于战斗部装填设计,能够提高战斗部在冲击波载荷下的安全性。     

济南市区加油站附近空气中有机污染特性研究

通过研究济南市市区某加油站邻近空气中挥发性有机物浓度的分布情形,分析加油站作业过程对周围环境空气的影响.结果表明:在加油等操作过程中,逸散排放的挥发性有机物主要为苯类污染物,其最大浓度值出现在逸散源附近,上风向浓度较下风向低,且种类较少.     

强化混凝对二级处理出水中溶解性有机物特性的影响

以沈阳市B污水处理厂二级处理出水为研究对象,采用FeCl3.6H2O作为混凝剂,研究了强化混凝对二级处理出水中溶解性有机物(DOM)的卤代活性和荧光特性的影响.按照DOM在XAD树脂上的吸附特性将其分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPI-A)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明,强化混凝(混凝剂投加量为80mg.L-1,pH=5.00)对DOC的去除率为55.3%.强化混凝对HPO-A的去除率最高,而对HPI的去除率最低.强化混凝后,HPO-N的三卤甲烷生成活性(STHMFP)上升,而其他4种DOM组分的STHMFP下降.强化混凝能够有效去除类富里酸荧光物质和具有高环数和高聚合度的稠环类芳香性荧光物质.强化混凝对DOM组分的去除率和DOM组分的荧光强度下降率的相关性不显著.     

可生物降解吸油材料发展现状与研究进展

综述了近年来国内外可生物降解吸油材料的发展情况，探讨了其相关的降解机理及目前可生物解吸油材料发展中仍存在的一些问题，并指出可生物降解吸油材料将具有广阔的应用前景。     

酚类化合物雌激素效应的比较研究

采用重组人雌激素受体基因片段(hER)及共激活因子(GRIP1)双杂交酵母检测体系,检测9种酚类物质的类雌激素和抗雌激素效应.结果表明,所检测的化合物中有3种同时表现出雌激素诱导与抑制活性;2种只表现出雌激素诱导活性;1种只表现出雌激素抑制活性;3种均没有雌激素诱导与抑制活性.结构分析表明:酚类中产生雌激素活性的物质具有取代基位于对位且邻位没有大的取代基团的结构;烷基在对位的酚类物质也能显示出雌激素拮抗活性.所采用的双杂交酵母检测体系适用于外源物质的雌激素活性检测,具有较高的灵敏度;结合外源物的雌激素诱导与抑制活性,用于分析污染物的体内作用方式.     

交通活动对公路两侧土壤和灰尘中重金属含量的影响

为了解公路交通带来的重金属污染及其在公路两侧土壤中的分布规律,对相关研究结果的分析表明,含铅汽油、润滑油的燃烧,汽车轮胎、刹车里村的机械磨损等是公路两侧土壤和灰尘中重金属污染的重要来源.机动车辆排放的含重金属颗粒物或直接沉积在路面灰尘中,或通过干湿沉降沉积在公路两侧的土壤中,使得公路两侧土壤和灰尘中重金属出现不同程度的积累.一般地,公路两侧土壤中重金属含量随着距公路距离的增加呈指数形式下降.公路两侧土壤中重金属的含量及其分布格局因受交通流量、车辆类型、地形与路况、绿化带配置和风、降雨等气象条件的影响而异.