某有色金属企业污水处理厂污水处理工艺

对有色金属冶炼过程中产生的废水按特征因子的不同进行分质处理。其中,高浓度氨氮废水采用三级氨氮吹脱、吸收工艺进行脱氨预处理;含砷酸性废水采用三段中和-铁盐混凝法预处理;经预处理废水混合后,采用石灰法分级沉淀处理废水中重金属离子;然后根据各单位对回用水水质的不同要求,对废水进行深度处理,实现了污水处理后全部回用,污水零排放的目的。并且对污水中的氨、石膏、镍等资源进行回收利用,为企业降低了运行成本,并且防止了二次污染。     

北京市地面街尘与径流中重金属的污染特征（Characteristics of Heavy Metals in Street Dusts and Urban Runoff in Beijing）

街尘作为城市各种污染物的载体和地表径流污染物的主要来源对水环境的影响日益受到关注.论文分析了北京市城区街尘与地表径流中重金属浓度和颗粒的粒径分布.结果表明:不同城市土地利用类型对街尘和径流中的重金属含量、颗粒粒径分布具有重要影响.在商业区、主要道路、住宅区、城中村4种土地利用类型中,街尘重金属浓度和地面单位面积重金属质量均以主要道路最高;径流重金属浓度由高到低顺序依次为:主要道路>城中村>居民区;主要道路和商业区街尘颗粒中细粒径占的比例较高,在全部土地利用类型的径流水样中颗粒物粒径分布差别不大;随着街尘中颗粒物粒径的减小,重金属浓度增加;街尘中小于149μm的颗粒物质量百分比和重金属浓度均较高,且在径流中这个粒径段的颗粒物含量也高,体积比达80%以上.建议在今后的城市街尘面源污染控制中应特别关注土地利用类型和街尘粒径的影响.     

贵阳市城市道路灰尘重金属铅污染及评价

对贵阳市城市道路灰尘重金属铅污染进行了研究。结果表明：2008年贵阳市各行政区道路灰尘中铅的含量按南明区、乌当区、白云区、花溪区、云岩区、小河区顺序分别为81.19～174.94mg/kg、54.33～177.62mg/kg、59.75～275.93mg/kg、59.45～143.41mg/kg、61.32～106.05mg/kg、57.84～115.53mg/kg,平均含量分别为110.94mg/kg、78.49mg/kg、105.35mg/kg、96.87mg/kg、81.51mg/kg、88.11mg/kg,分别为环境背景值的3.0倍、2.1倍、2.8倍、2.6倍、2.2倍、2.4倍;不同行政区铅含量存在较大差异,铅在空间分布上也存在较大差异,其中白云区差异最大,云岩区差异最小。地积累指数及铅污染指数评价表明：贵阳市城市道路灰尘中铅污染总体上处于轻度污染水平,但局部区域处于偏中度至中度污染水平。     

兰州远郊区黑碳气溶胶浓度特征

利用兰州大学半干旱气候与环境观测站(SACOL)2007年1月1日至2009年8月28日黑碳气溶胶浓度和同期常规气象资料,分析了兰州远郊区黑碳气溶胶浓度特征.结果表明,该区黑碳气溶胶日平均浓度为1568ng/m3,低于东部地区区域本底站浓度,表明该地区污染较轻;黑碳浓度具有明显的季节变化,从春季到冬季平均浓度依次增大,分别为1234.74,1290.23,1669.06,2088.73ng/m3,日变化具有明显的双峰结构,最大值出现在09:00,最小值出现在17:00.黑碳浓度的变化特征与本地区的盛行风向、人类活动及天气过程有密切关系.沙尘气溶胶对黑碳浓度的影响取决沙尘过程的强度、沙尘携带的人为污染物的种类及数量、黑碳颗粒被其他气溶胶混合和包裹的程度.统计分析得出该地区大气黑碳气溶胶本底浓度约为1000ng/m3.     

港口煤翻车机房粉尘污染捕集的设计与应用

对煤翻车机房煤尘的污染现状进行了实际测量与数据分析,得到煤尘上扬的数学模型,设计了翻车机房扬尘的捕集系统,并对系统内各个装置的功能进行了分析。采用吹、吸互补并利用导流板的捕尘方式,使无序飞扬的粉尘变成了有序的流动,该方法解决了大区域、复杂工况环境捕集粉尘的问题。     

福州市公交枢纽站地表灰尘重金属含量、来源及其健康风险评价

城市地表灰尘中的重金属已成为城市环境和人类健康最重要的威胁之一. 为评价地表灰尘重金属的污染水平,研究了福州市公交枢纽站地表灰尘中的重金属质量分数、来源及其可能产生的健康风险. 结果表明:福州市公交枢纽站地表灰尘中w(Cr)、w(Cu)、w(Zn)和w(Cd)分别是福州市城区土壤的2.74、4.21、4.01和4.68倍. 灰尘中重金属Co、Ni和Mn主要来源于城市土壤,Cd、Pb和Cu来源于交通运输过程,Cr来源于城市土壤和交通运输,Zn主要来源于交通运输、城市生活污染和工业活动等复合污染源. 不同暴露途径的重金属暴露剂量和非致癌风险大小排序为消化道>皮肤接触>呼吸吸入. 地表灰尘中重金属非致癌总风险为儿童高于成人. 致癌重金属的暴露风险为Cd>Ni>Cr. 城市公交枢纽站地表灰尘中重金属污染受交通运输影响较大.      

尘卷风对沙尘气溶胶的贡献及其与太阳辐射的关系

利用塔克拉玛干沙漠及周边地区观测资料,依据尘卷风热力学理论和方法,估算出在塔克拉玛干沙漠地区尘卷风对沙尘气溶胶贡献的年平均量为4.0× 106t,年最大量为5.0×106t,与该地区沙尘暴的沙尘气溶胶年均贡献量相当.依赖于太阳辐射强度季节变化,尘卷风的起沙量具有与地面温度同步的季节变化规律.     

夏季学生宿舍室内降尘中PAEs污染特征和暴露评价

利用CH2Cl2和超声对35个南开大学学生宿舍室内降尘样品中的DMP、DEP、DBP、BBP、DEHP 和DOP等6种PAES进行提取分离,采用GC-MS定量分析,研究了PAEs污染变化特征及暴露风险.结果表明,南开大学学生宿舍室内降尘中PAEs污染以DEHP和DBP为主,中位值浓度分别为126.916μg/g和123.591μg/g,两者之和占Σ6PAEs浓度的99%以上,室内降尘中PAEs污染程度和类型与室内含增塑剂产品的数量、室内清洁通风情况及成员性别有关;经口暴露水平大于皮肤,其中DBP、DEHP的暴露量高于美国,占人体总PAEs摄入量比例较高,故学生宿舍降尘中PAEs暴露应给予重视.     

Suitability of various chemically prepared activated carbons for the removal of copper(II) ions

Studies on the suitability of various chemically prepared activated carbons (CPACs) like straw carbon (SC), sawdust carbon (SDC), dates nut carbon (DNC) and commercial activated carbon (CAC) for the removal of copper(II) ions by adsorption from simulated wastewater have been carried out under batch mode at 30?±?1°C and the results are compared. The percentage removal of Cu(II) ions increased with a decrease in initial concentration, particle size and added electrolytes (ionic strength) and increased with an increase in contact time, dose of adsorbent and initial pH of the solution. The adsorption data were fitted with the Langmuir isotherm. The applicability of the first order kinetic equation viz. Lagergren equation was tested by correlation analysis. The adsorption process is concluded to be a spontaneous, first order reaction, occurring with increased randomness at the solid–liquid interface. Studies on the desorption of Cu²⁺-loaded activated carbons (ACs) were carried out with nitric acid (0.2–1?N). The possibility of reuse of the regenerated ACs in cycle (in cue-one after another) was tested. SC was found to be a suitable adsorbent alternative to CAC among CPACs for the removal of metal ions, in general, and Cu²⁺ ions, in particular.     

Size-resolved aerosol ionic composition and secondary formation at Mount Heng in South Central China

To understand the size-resolved aerosol ionic composition and the factors influencing secondary aerosol formation in the upper boundary layer in South Central China, size-segregated aerosol samples were collected using a micro-orifice uniform deposit irnpactor （MOUDI） in spring 2009 at the summit of Mount Heng （1269 m asl）, followed by subsequent laboratory analyses of 13 inorganic and organic water-soluble ions. During non- dust-storm periods, the average PM1.8 concentration was 41.8 μg·m^-3, contributing to 55% of the PM10. Sulfates, nitrates, and ammonium, the dominant ions in the fine particles, amounted to 46.8% of the PM1.8. Compared with Mount Tai in the North China Plain, the concentrations of both fine and coarse particles and the ions contained therein were substantially lower. When the air masses from Southeast Asia prevailed, intensive biomass burning there led to elevated concentrations of sulfates, nitrates, ammonium, potassium, and chloride in the fine particles at Mount Heng. The air masses originating from the north Gobi brought heavy dust storms that resulted in the remarkable production of sulfates, ammonium, methane sulfonic acid, and oxalates in the coarse particles. Generally, the sulfates were primarily produced in the form of （NH4）2SO4 in the droplet mode via heterogeneous aqueous reactions. Only approximately one-third of the nitrates were distributed in the fine mode, and high humidity facilitated the secondary formation of fine nitrates. The heterogeneous formation of coarse nitrates and ammonium on dry alkaline dust surfaces was found to be less efficient than that on the coarse particles during non-dust-storm periods.