建材资源开发的生态环境补偿费探讨

应用新的资源价值观念与环境经济学中ＭＯＣ框架及其它理论，给出了建材资源的生态环境补偿费的定义与确定方法，建立了相应的理论模型。在此基础上，根据不同地区的经济发展水平与环境现状等实现情况，用认可系数对计算的补偿费进行修正。     

浦东新区大气气溶胶中碳颗粒的分布规律

采用元素相关性分析方法，找出浦东新区大气气溶胶中碳颗粒的污染源，确证该区大气中碳颗粒主要来自煤的燃烧。同时初步找出浦东新区大气中碳颗粒污染的时空分布和粒径分布规律，为改善浦东 新区大气污染状况提供依据。     

分光光度法测定水样中铬

在ｐＨ４．４ＨＡＣ－ＮａＡｃ缓冲介质及乳化剂ＯＰ存在下，Ｃｒ６＋与二溴羟基苯基荧光酮（ＤＢＨＰＦ）显色反应生成桔红色络合物．该络合物最大吸收位于４８２ｎｍ波长处，表现摩尔吸光系数εｍａｘ＝３．４７×１０４．络合物配位比为Ｃｒ６＋：ＤＢＨＰＦ＝２：３，Ｃｒ６＋在０－１６μｇ／２５ｍＬ范围内遵守比耳定律．方法已用于水样中微量铬的测定，结果满意．     

气相色谱法测定室内空气中挥发性卤代烃

建立了活性炭吸附-溶剂解吸-气相色谱测定室内空气中7种挥发性卤代烃的分析方法。样品经活性炭采样管富集后,用二硫化碳解吸,Agilent HP-1色谱柱分离,使用带有电子捕获检测器的气相色谱仪测定,以保留时间定性,外标法定量。当采样体积为10 L时,方法检出限范围是0.03~0.18 g/m3,加标回收率在72%~114%之间,相对标准偏差小于15%。结果表明,该方法可以应用于室内空气中痕量挥发性卤代烃样品的检测分析。     

Daily Bank Erosion Rates in the Lower Yellow River Before and After Dam Construction

During the period of water impoundment and sediment detention of the Sanmenxia Reservoir, riverbank erosion processes played a key role in the channel evolution of the Lower Yellow River (LYR). However, research into bank erosion rates of the LYR has been neglected due to the lack of direct field monitoring. In this study, an indirect method is proposed to determine bank erosion rates at daily time scales by outlining a detailed calculation procedure using measured hydrological data. A total of 810 data points of daily bank erosion rates before and after the construction of Sanmenxia Dam was calculated at seven hydrometric sections along the LYR, with the corresponding values of the bank stability coefficient and the width‐to‐depth ratio also being calculated. Empirical relations were then developed to estimate the daily bank erosion rates, using these parameters at the sections. Temporal and spatial variability in daily bank erosion rates in the LYR before and after dam construction were also investigated, revealing that: (1) the bank erosion rates had a mean value of 16.7‐29.1 m/day in the braided reach, with a maximum value of 290.0 m/day, while they were relatively low in the meandering reach, with a mean value of 2.5 m/day; (2) the erosion rates before dam construction were slightly greater than those after dam construction, with the difference reaching 5‐10 m/day in the braided reach, decreasing in the transitional reach gradually, and being slight in the meandering reach.     

Precise and Economical Dredging Model of Sediments and Its Field Application: Case Study of a River Heavily Polluted by Organic Matter,Nitrogen, and Phosphorus

Environmental dredging is an efficient means to counteract the eutrophication of water bodies caused by endogenous release of nitrogen and/or phosphorus from polluted sediments. The huge operational cost and subsequent disposal cost of the dredged polluted sediments, as well as the adverse effect on the benthic environment caused by excessive dredging, make the currently adopted dredging methods unfavorable. Precise dredging, i.e., determining the dredging depth based on the pollution level, not only significantly decreases the costs but also leaves a uniform favorable environment for benthos. However, there is still no feasible process to make this promising method executable. Taking a river heavily polluted by organic compounds as an example, we proposed an executable precise dredging process, including sediment survey, model establishment, data interpolation, and calculation of dredging amount. Compared with the traditional dredging method, the precise one would save 16 to 45 % of cost according to different pollutant removal demands. This precise dredging method was adopted by the National Water Project of China to treat the endogenous pollution of Nanfei River in 2010. This research provides a universal scientific and engineering basis for sediment dredging projects.     

Occurrence and behaviour of nonylphenol and octylphenol in Nanming River, Guiyang City, China

Occurrence, variation and behaviour of nonylphenol (NP) and octylphenol (OP) were studied in surface water and groundwater in Guiyang, Guizhou Province, southwestern China. Discharge of wastewater from Guiyang City was the main source of alkylphenols (APs) entering the aquatic environment. The concentrations of NP and OP in river water ranged from 40 to 1582 ng L(-1) and from below the lowest limit of detection (LOD) to 67 ng L(-1), respectively. NP and OP were also detected in groundwater. Both NP and OP exhibited spatial and temporal variations in river water and groundwater. It was found that concentrations of NP and OP in river water was low upstream and dramatically increased downstream, and higher concentration of NP was found in winter compared to that in summer. Proportions of NP and OP were trapped by suspended particulate matter (SPM), which accounted for 7.6-50.0% and 3.4-25.6% of their total concentration in the river water system, respectively. Seasonal changes in water flow were responsible for the temporal variations of APs. To determine the behaviour of APs along the river, a mass balance equation based on chloride was used. The results showed that a mixing process was the predominant factor to determine upstream APs concentrations; while the discharge of wastewater controlled the concentrations of APs downstream. Considering the adverse effect of APs on organisms, combined effect modeling was used to assess the toxicity to fish. It was found that the predicted mixture effect for APs in river water on fish vitellogenin induction was low upstream and medium downstream, respectively.     

Penetration of polar brominated DBPs through the activated carbon columns during total organic bromine analysis

Total organic bromine (TOBr) is a collective parameter representing all the brominated organic disinfection byproducts (DBPs) in water samples. TOBr can be measured using the adsorption-pyrolysis method according to Standard Method 5320B. This method involves that brominated organic DBPs are separated from inorganic halides and concentrated from aqueous solution by adsorption onto the activated carbon (AC). Previous studies have reported that some commonly known brominated DBPs can partially penetrate through the AC during this adsorption step. In this work, the penetration of polar brominated DBPs through AC and ozone-modified AC was explored with two simulated drinking water samples and one chlorinated wastewater effluent sample. Polar brominated DBPs were selectively detected with a novel precursor ion scan method using electrospray ionization-triple quadrupole mass spectrometry. The results show that 3.4% and 10.4% of polar brominated DBPs (in terms of total ion intensity) in the chlorinated Suwannee River fulvic acid and humic acid samples, respectively, penetrated through the AC, and 19.6% of polar brominated DBPs in the chlorinated secondary wastewater effluent sample penetrated through the AC. The ozone-modification of AC minimized the penetration of polar brominated DBPs during the TOBr analysis.     

Sorption of phthalate acid esters on black carbon from different sources

Black carbon (BC) is known as a strong sorbent for the sorption of planar hydrophobic organic compounds (HOCs), but there is very little information about the sorption of nonplanar HOCs on BC. In this study, the sorption of di-(2-ethyl-hexyl) phthalate (DEHP), one kind of nonplanar phthalate acid ester (PAE), by environmental BC collected from river sediments and pure BC (char-wood, char-stalk and soot-ash) was investigated. Strong and nonlinear sorption was observed for the sorption of DEHP on both pure BC and environmental BC with the Freundlich exponent ranging from 0.55 to 0.75 except for soot-ash, and the measured K(BC) (BC-water partition coefficient) of DEHP was about one order of magnitude higher than its organic carbon-water partition coefficient. There was a significant difference in sorption capacity among the environmental and pure BC. The presence of di-methyl phthalate (DMP) could significantly decrease the sorption of DEHP on BC, especially for environmental BC. In addition, the contribution of BC to the total sorption of DEHP on original river sediments was more than 50% when the equilibrium concentration of DEHP was less than 10 μg L(-1). This study indicated that ortho-substituted nonplanar PAEs could also be strongly sorbed by BC, and the difference in sorption among the BC samples revealed that it is important to take the source of BC into account when assessing its effects on the fate of HOCs in aquatic environment.     

Aerosol size distributions in urban Jinan: Seasonal characteristics and variations between weekdays and weekends in a heavily polluted atmosphere

Aerosol size distributions, trace gas, and PM(2.5) concentrations have been measured in urban Jinan, China, over 6 months in 2007 and 2008, covering spring, summer, fall, and winter time periods. Number concentrations of particles (10-2,500 nm) were 16,200, 13,900, 11,200, and 21,600 cm(?-3) in spring, summer, fall, and winter, respectively. Compared with other urban studies, Jinan has higher number concentrations of accumulation-mode particles (100-500 nm) and particles (10-2,500 nm), but lower concentrations of ultrafine particles (10-100 nm). The number, surface and volume concentrations, and size distributions of particles showed obvious seasonal variation and are also influenced by traffic emissions. Through correlation analysis, traffic emissions are proposed to be a more important contributor to Atkien-mode and accumulation-mode particles than coal firing. Around midday, the presence of nanoparticles and new particle formation is limited to pre-existing particles from traffic emissions and the mass transport of particles from suburban and rural areas. Compared with other studies in urban areas of Europe and the USA, the variation of particle number concentration and related gas concentration in Jinan between weekdays and weekends is smaller and the reasons has been deduced.