沙漠油田开发生态环境保护的实践

文章阐述了地处沙漠腹地的石西油田在开发建设过程中开展环境保护工作的具体做法,从加强组织领导、制定并不断完善环保规章制度、加大科技投入等方面分析总结了在沙漠油田中开展环境保护的管理经验,通过加强井场作业、油气集输、建设用地管理、植物种植管理方面的措施,阐述了在沙漠油田开发建设中创建绿色油气田活动所取得的成绩。     

Optimizing model for land use/land cover retrieval from remote sensing imagery based on variable precision rough sets

The suitable spectral mode in remote sensing is often desirable to facilitate the inversion of ecological environment and landscape. This paper put forward an optimizing model based on variable precision rough sets (VPRS) for the land cover discrimination in wetland inventory. In the case study of Lake Baiyangdian which has important ecological functions to the northern China, this model is established successfully according to the domain-experts knowledge. The procedure is as follows. First step is data collection, including remote-sensing data (e.g., Landsat-5 TM bands), the digitized relief maps, and statistical yearbooks. Second, the remote sensing imagery (RSI) and relief maps are co-registered into the same resolution. Third, a condition set, including various attributes is derived from spectral bands, band math or ratio indices based on previous studies, at the same time, the decision set is derived from true land types after investigation and validation. Then, the remote sensing decision table (RSDT) is constructed by linking condition set with decision set according to the sequential pixels in RSI. Fourth, we create one forward greedy searching algorithm based on VPRS to handle this RSDT. After adjusting parameters such as β and knowledge granularity diameter (KGD), we obtain the stable optimized results. Comparative experiments and evaluation show that the discrimination or retrieval accuracy of VPRS model is satisfying (overall accuracy: 87.32% and KHAT: 0.84) and better than original data. Moreover, data dimension has been decreased dramatically (from 12 to 3) and key attributes found by the model may be useful for specific retrieval in wetland inventories.     

Heat of absorption of CO2 in aqueous ammonia and ammonium carbonate/carbamate solutions

A reaction calorimeter was used to determine the enthalpies of absorption of CO₂ in aqueous ammonia and in aqueous solutions of ammonium carbonate at temperatures of 35–80 °C. The heat of absorption of CO₂ with 2.5 wt% aqueous ammonia solution was found to be about 70 kJ/mol CO₂, which is lower than that with MEA (around 85 kJ/mol) at 35 and 40 °C. The value decreases with increased loading, but not to as low a value as expected by the carbonate–bicarbonate reaction (26.88 kJ/mol). The enthalpy of absorption of CO₂ in aqueous ammonia at 60 and 80 °C decreases with loadings at first, then increases between 0.2 mol CO₂/mol NH₃ and 0.6 mol CO₂/mol NH₃, and then decreases again. The behavior of the heat of absorption of CO₂ in 10 wt% ammonium carbonate solution was found to be the same as that of aqueous ammonia at loadings above 0.6 mol CO₂/mol NH₃. The heat of absorption increases with increasing temperature. The heats of absorption are directly related to the extent of the various reactions with CO₂ and can be assessed from the species variation in the liquid phase.     

Assessment of elemental distribution and trace element contamination in surficial wetland sediments, Southern Tibetan Plateau

In order to analyze and evaluate different trace metals on surface water of the Changjiang River, concentrations of dissolved trace metals (Cu, Ni, Fe, Co, Sc, Al, Zn, Pb, Cd, Se, As, Cr, and Hg), major elements(Ca and Mg), and nutrient(NO $_{3}^{-})$ were measured. Samples were taken at 76 positions along Changjiang River in flood and dry seasons during 2007?C2008. Spatial distributions identified two main large zones mainly influenced by mineral erosion (sites 1?C22) and anthropogenic action (sites 23?C76), respectively. Principal component analysis (PCA) and hierarchical cluster analysis were used to identify the variance distinguishing the origin of water. Four significant components were extracted by PCA, explaining 74.91% of total variable. Cu, Ni, Fe, Co, Sc, Al, Ca, and Mg were mainly associated with the weathering and erosion of various rocks and minerals, while an anthropogenic source was identified for Cd and As. Although erosion was one source of Pb and Zn, they were also input by atmospheric deposition and industrial pollutions. NO $_{3}^{-}$ and Se were mainly associated with agriculture activities. However, Hg and Cr showed different sources. CA confirmed and completed the results obtained by PCA, classifying the data into two large groups representing different areas. Group 1 referred to the upper reaches which represented samples mainly corresponding to natural background areas. Group 2 referred to the middle and lower reaches including samples under anthropogenic influence. Meanwhile, group 2 was subdivided into three new groups, representing agricultural, industrial, and various artificial pollution sources, respectively.     

Chemical composition of precipitation and its sources in Hangzhou, China

To understand the origin and chemical characteristics of precipitation in Hangzhou, rainwater samples were collected from June 2006 to May 2008. All samples were analyzed for pH, electrical conductivity, and major ions (NH??, Ca2?, Mg2?, Na?, K?, SO?2?, NO??, F?, and Cl?). Acidification of precipitation in Hangzhou was serious with volume-weighted mean pH value of 4.5, while frequency of acid rain was 95%. The calculated SO?2?/NO?? ratio in Hangzhou precipitation was 2.87, which indicated that the precipitation of Hangzhou belonged to sulfate-based acid rain. The results of acid neutralization analysis showed that not all the acidity in the precipitation of Hangzhou was neutralized by alkaline constituents. The results of sea salt contribution analysis showed that nearly all SO?2?, Ca2?, and Mg2? and 33.7% of K? were of non-sea origins, while all Na? and Cl? and 66.3% of K? originated from sea sources. The principal component analysis which was used to analyze the sources of various ions indicated that chemical compositions of precipitation in Hangzhou mainly came from terrestrial sources, factory emissions, fuel wood burning, and marine sources.     

Polycyclic aromatic hydrocarbons in effluents from wastewater treatment plants and receiving streams in Tianjin, China

Surface water, suspended particulate matter, pore water, and sediment samples were collected and analyzed for polycyclic aromatic hydrocarbons (PAHs) in Yongding New River, South Drainage Canal and North Drainage Canal, which receive most of wastewater from industrial city of Tianjin. PAH concentrations in effluent samples of wastewater treatment plants (WTP) discharging into the South Drainage Canal and North Drainage Canal were quantified for the first time. The results showed that the discharge of the WTPs recently only contributed to the PAH contamination in the canals near the outlets of the WTPs. PAH levels in sediments of the streams were greatly higher than those in soils by riverbank probably due to receiving large amounts of untreated wastewater. Unusually high benz[a] anthracene concentration strongly influenced the seasonal and spatial variation of total PAH concentrations in South Drainage Canal. Paired samples t test of ??Nap, Fl, Phe, Fluo and ??Nap, Phe, Fluo, Chry concentrations, which were dominant components in the air samples from non-heating and heating season, respectively, in the suspended particulate matters from the streams showed that PAH source from air deposition was more important for Yongding New River than that for South Drainage Canal and North Drainage Canal. Source apportionment based on PAH profiles indicated that coal combustion was the major PAH contamination source, and coke oven sources and wood combustion also contributed to the PAH contamination of the streams. This was further indicated by organic petrography analysis.     

Sorption of DDTs on biofilms, suspended particles and river sediments: effects of heavy metals

The sorption by solid materials is one of the most important processes that affect the fate of hydrophobic organic pollutants in aquatic systems. Current studies focus on the sorption of hydrophobic pollutants by single natural solid material, whereas few studies compared the sorption behaviors of different solids. Furthermore, natural aquatic environment is a complex system where hydrophobic pollutants coexist with many other pollutants, but only limited studies reported the effects of coexisting components on the sorption. Here we studied the sorption of dichlorodiphenyltrichloroethanes (DDTs) by three common solids in natural water, i.e., biofilms, suspended particles and sediments. The effects of typical coexisting heavy metals on the sorption were also examined. The results show that the sorption is described by a dual-mode sorption model. Compared with sediments, more DDTs were sorbed by biofilms and suspended particles. Coexisting Pb, Cd and Cu increased the sorption of DDTs on sediments while decreasing the sorption on biofilms slightly, with little effect on the sorption on suspended particles. The different sorption behaviors of the solids were mainly determined by the composition of the solids: more organics were observed in biofilms and suspended particles.     

基于耗散结构理论的驾驶中人因失误分析研究

通过对耗散结构理论的分析,建立了驾驶系统的耗散结构动态模型。基于此模型,从负熵流、扰动、非线性机制以及系统的初始稳定值几个方面对驾驶中人因失误出现的原因进行了分析。文章将耗散结构理论作为分析人因失误的工具,为研究驾驶中的人因失误提供了一种新的视角。     

玉米淀粉粉尘爆炸危险性研究

为研究玉米淀粉粉尘爆炸危险性,采用哈特曼管式爆炸测试装置和20 L球爆炸测试装置对200目(<75μm)以下的玉米淀粉粉尘爆炸危险性进行评估,基于静电火花和粉尘质量浓度对粉尘爆炸的影响,对玉米淀粉的静电火花最小点火能量、爆炸下限质量浓度、最大爆炸压力和爆炸指数进行了研究,根据试验结果对玉米淀粉爆炸危险性进行分级。试验结果表明:温度在25℃,喷粉压力为0.80 MPa,粉尘质量浓度在250～750 g/m3范围内,粉尘的最小点火能量随着粉尘质量浓度增加而降低,其最小点火能量在40～80 mJ之间;在点火能量为10 kJ时,粉尘爆炸下限质量浓度在50～60 g/m3之间;在粉尘质量浓度为750 g/m3时,爆炸压力达到最大,为0.66 MPa;在粉尘质量浓度为500 g/m3时,爆炸指数达到最大,为17.21 MPa.m/s,其粉尘爆炸危险性分级为Ⅰ级。     

省内公路可移动危险源的模糊综合安全预警

为了对公路可移动危险源进行有效控制,分析了影响公路可移动危险源危险程度的因素,采用模糊综合评判方法,并通过公路可移动危险源模糊预警系统实现了公路可移动危险源的实时综合安全预警.结果表明,此方法考虑危险因素较全面,且可在屏幕实时显示各公路可移动危险源的预警结果,有利于提高安全管理水平.