淮南市平山头水源地水中PAEs污染情况分析

以淮南市平山头水厂水源4种邻苯二甲酸酯类（PAEs）：邻苯二甲酸二甲酯（DMP）、邻苯二甲酸二乙酯（DEP）、邻苯二甲酸丁基苄基酯（BBP）、邻苯二甲酸二丁酯（DBP）为研究对象,研究了水源地水中PAEs的污染情况。研究结果表明：DMP、DEP、BBP、DBP的检出率分别为50％、83．3％、83．3％、100％,DBP的达标率为100％;DMP、DEP、BBP、DBP对∑4PAEs污染的贡献率依次为：5．2％、3．7％、20．1％、71．1％,说明平山头水厂水源地水中PAEs污染主要以DBP为主。水源地各采样点∑4PAEs的含量范围0．632～1．623μg／L,其采样断面平均浓度顺序为：上游〉中游〉下游。     

Recent development of a refined multiple air pollutant emission inventory of vehicles in the Central Plains of China

Central Plains region of China,represented by Henan Province,is facing serious air pollution problems.Vehicular exhaust emissions had adverse impacts on the atmospheric environment.The first comprehensive and novel vehicle emission inventory for Henan Province using vehicle kilometers traveled,localized emission factors,and activity data at city-level was developed.Furthermore,3 km×3 km gridded emission and temporal variations were determined by using localized information.Results show that the total emissions of sulfur dioxide(SO_2),nitrogen oxides(NOx),carbon monoxide(CO),particular matter with aerodynamic diameter10μm(PM_(10)),aerodynamic diameter2.5μm(PM_(2.5)),volatile organic compounds(VOCs),VOCs-evaporation and ammonia in 2015 were 9.1,533.4,1190.7,23.7,21.6,150.8,31.5 and 10.4 Gg,respectively,and the emission intensities of the above pollutants were 0.05,2.7,6.0,0.1,0.1,0.8,0.2 and 0.05 g/km,respectively.Vehicles meeting the Primary China 1,China 3 and China 4 contributed 89.1%,82.7%,75.3%,75.5%,75.5%,68.2%,68.4%and 82.3%for SO_2,NO_x,CO,PM_(10),PM_(2.5),VOCs,VOCs-evaporation and ammonia emissions,respectively.Zhengzhou,Zhoukou,Nanyang,Luoyang,Shangqiu and Xinyang showed relatively higher emissions and contributed more than 50%of each pollutant.The spatial distribution indicated obvious characteristics of the road network,and high-level emission was concentrated in the downtown areas.Additionally,the ozone formation potential(OFP)based on the estimated speciated VOC emissions was 569.6 Gg in Henan Province.Aliphatic and aromatic hydrocarbons were the main species of VOCs,whereas olefins contributed the largest proportion of OFP,with 42.2%.     

Chemical characterization of size-resolved aerosols in four seasons and hazy days in the megacity Beijing of China

Size-resolved aerosol samples were collected by MOUDI in four seasons in 2007 in Beijing. The PM₁₀ and PM_1.8 mass concentrations were 166.0 ± 120.5 and 91.6 ± 69.7 μg/m³, respectively, throughout the measurement, with seasonal variation: nearly two times higher in autumn than in summer and spring. Serious fine particle pollution occurred in winter with the PM_1.8/PM₁₀ ratio of 0.63, which was higher than other seasons. The size distribution of PM showed obvious seasonal and diurnal variation, with a smaller fine mode peak in spring and in the daytime. OM (organic matter = 1.6 × OC (organic carbon)) and SIA (secondary inorganic aerosol) were major components of fine particles, while OM, SIA and Ca^2 + were major components in coarse particles. Moreover, secondary components, mainly SOA (secondary organic aerosol) and SIA, accounted for 46%–96% of each size bin in fine particles, which meant that secondary pollution existed all year. Sulfates and nitrates, primarily in the form of (NH₄)₂SO₄, NH₄NO₃, CaSO₄, Na₂SO₄ and K₂SO₄, calculated by the model ISORROPIA II, were major components of the solid phase in fine particles. The PM concentration and size distribution were similar in the four seasons on non-haze days, while large differences occurred on haze days, which indicated seasonal variation of PM concentration and size distribution were dominated by haze days. The SIA concentrations and fractions of nearly all size bins were higher on haze days than on non-haze days, which was attributed to heterogeneous aqueous reactions on haze days in the four seasons.     

略论大气污染物总量控制方法

本文阐述了大气污染物总量控制的基本方法,内容包括:排放源数据,计算网络划分,污染源在网格中的安放,大气污染总量控制设计条件和方法,总量控制模型,计算参数选择,采样时间和衰减修正,模式的校准。最后介绍了总量控制优化模型。     

在微波辐射下用ACF处理吲哚溶液的实验研究

在ACF存在下微波辐射能除去焦化废水中的吲哚污染物。实验研究了微波辐射时间。微波功率，吲哚溶液初始浓度，pH值等因素对微波处理吲哚溶液的影响。并用活性炭代替ACF作了对比实验，实验结果表明，在微波辐射下，用ACF处理吲哚溶液具有明显高的效果，3.5min去除率即可达98%，微波辐射不能使吲哚发生降解。其作用是使ACF的孔隙结构发生变化，增加了其吸附能力。     

膜生物反应器工艺参数控制研究

以外压管式膜生物反应器和中空纤维一体式膜生物反应器处理城市污水试验为基础,对膜生物反应器工艺参数控制进行了研究。试验首次建立了曝气池容积与膜面积比的计算关系式,即V/A=J·S_O/N·X。验证了膜通量与污泥浓度的对数呈线性关系,污泥浓度愈高,膜通量愈低。还讨论了HRT和SRT对膜生物反应器生物性能以及出水水质的影响。     

天津冬季PM2.5与PM10中有机碳、元素碳的污染特征

研究了天津冬季PM2.5和PM10中碳成分的污染特征.结果表明,天津冬季PM2.5和PM10的平均质量浓度分别为(124.4±60.9)、(224.6±131.2)μg/m3;总碳(TC)、有机碳(OC)与元素碳(EC)在PM2.5中的平均质量分数比在PM10中分别高出5.0%、3.6%、1.2%;PM2.5中OC、EC的相关系数较高,为0.95,表明OC、EC的来源相对简单,可能主要反应了燃煤和机动车尾气的贡献.OC/EC的平均值在PM2.5和PM10中分别为3.9、4.9.次生有机碳(SOC)在PM2.55和PM10中的平均质量浓度分别为14.9、23.4/μg/m3,分别占OC的48.5%(质量分数,下同)、49.8%,OC/EC较高可能主要与直接排放源有关;PM2.5中的OC1与OC2的比例明显高于PM10,而聚合碳(OPC)的比例又低于PM10,同时PM2.5与PM10中的EC1含量均较高,表明天津冬季燃煤取暖和机动车尾气是重要的污染源.     

厌氧、缺氧、好氧多级交替SBR脱氮除磷试验研究

以实际生活污水为研究对象,采用厌氧、缺氧、好氧多级交替序批式反应器(SBR)工艺,通过曝气时间、交替次数的凋整对该系统的脱氮除磷效果进行了研究,最终将工艺确定为厌氧1.5 h-好氧1.0h-缺氧1.0h-好氧20 min-缺氧 1.0 h-好氧20min.试验结果表明:该系统与传统的SBR相比节省了44%的曝气量,且对COD、TN、TP去除率分别达85%、78%、99.5%,同时发现曝气过程 NO2-N和NO3-N的累积可能会对好氧吸磷产生抑制作用.     

活性炭纤维吸附废水中对硝基苯酚及其脱附研究

采用新型高效吸附剂--活性炭纤维吸附废水中对硝基苯酚,对其吸附和脱附影响因素进行了较详细的研究,确定了最佳工艺参数,并对动态吸附-脱附进行了稳定性实验.在最佳的吸附条件下,装填4 g活性炭纤维可处理含对硝基苯酚1000 mg/L的废水1400 mL,出水对硝基苯酚浓度＜2 mg/L,达到国家综合污水一级排放标准,活性炭纤维有效吸附量可达349.87 mg/g.在最佳脱附条件下,脱附率＞99%,并可从高浓度脱附液中回收对硝基苯酚.稳定性实验表明,吸附-脱附性能稳定,采用活性炭纤维吸附处理对硝基苯酚废水是一种行之有效的处理方法.     

阿尔泰多拉纳萨依金矿床初探

新疆多拉纳萨依金矿床位于阿尔泰克兰海西褶皱带玛尔卡库里大断裂的西南侧,西与苏联矿区阿尔泰之列宁诺戈尔斯克—孜里亚诺夫斯克构造成矿亚带相接。地层为中泥盆统托克萨雷组浅变质岩,大致呈南北走向的长条状分布在三个斜长花岗岩侵入体之间,并有许多钠长斑岩岩脉穿插。主要构造线方向为北北东,向西倾斜。金矿体赋存在沿断裂带侵入于灰岩中的石英钠长岩(或钠长石化斜长花岗岩)中。蚀变围岩主要为千糜岩化、白云母化的石英钠长岩。石英脉中金的品位虽然较高,但工业储量主要赋存于蚀变围岩中。自然金主要以显微和次显微状独立矿物被包裹于黄铁矿等矿物中,成色很高(932—967),其中的少量元素为银、汞和铋。为与斜长花岗岩有关的岩浆期后高—中温热液充填—交代矿床。