Sedimentary record of polycyclic aromatic hydrocarbons in Lake Erhai, Southwest China

The temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in a sediment core from Lake Erhal in Southwest China using gas-chromatography/mass spectrometry (GC/MS) method.The total organic carbon (TOC) normalized total PAHs concentrations (sum of US Environmental Protection Agency proposed 16 priority PAHs) ranged from 31.9 to 269 μg/g dry weight (dw),and were characterized by a slowly increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments.The PAHs in the sediments were dominated by low molecular weight (LMW) PAHs,suggesting that the primary source of PAHs was low- and moderate temperature combustion processes.However,both the significant increase in high molecular weight (HMW) PAHs in the upper sediments and the vertical profile of diagnostic ratios pointed out a change in the sources of PAHs from low-temperature combustion to high-temperature combustion.The ecotoxicological assessment based on consensus-based sediment quality guidelines implied that potential adverse biological impacts were possible for benzo(ghi)perylenelene and most LMW PAHs.In addition,the total BaP equivalent quotient of seven carcinogenic polycyclic aromatic hydrocarbons (BaA,CHr,BbF,BkF,BaP,DBA and INP) was 106.1 ng/g,according to the toxic equivalency factors.Although there was no great biological impact associated with the HMW PAlls,great attention should be paid to these PAH components based on their rapid increase in the upper sediments.     

Adsorption of zinc on manganite(γ-MnOOH): particle concentration effect and adsorption reversibility

The adsorption and desorption processes of Zn(Ⅱ) on τ-MnOOH as a function of particle concentrations (Cp) were studied. An obvious Cp effect was observed in this adsorption system. The degree of adsorption hysteresis increased greatly with the increasing of Cp, indicating that the extent of the real metastable-equilibrium states deviating from the ideal equilibrium state was enhanced with the increasing of Cp. The Cp-reversibility relationship confirmed the metastable-equilibrium adsorption (MEA) inequality (Pan, 1998a), which was the core formulation of the MEA theory. Because the MEA inequality was based on the basic hypothesis of MEA theory that adsorption densitιy ι is not a state variable, the Cp-reversibility relationship gave indirect evidence to the basic hypothesis of MEA theory.     

RBCA、CLEA及CalTOX模型在苯并[a]芘污染场地健康风险评估中的应用比较

为探讨不同模型对污染场地健康风险评估结果的影响,以苯并[a]芘为例,采用RBCA、CLEA和CalTOX模型对某工业污染场地表层土壤进行健康风险评估,分析了评估结果的差异和原因,同时对模型的主要暴露参数进行了敏感性分析,并推导出基于风险概率分布的土壤修复限值.结果表明,RBCA、CLEA和CalTOX模型计算的苯并[a]芘致癌总风险分别为2.40×10-4、632×10-4和7.04×10-6,且经口摄入和皮肤接触2个途径对人体健康造成的危害最大.降解作用是影响CalTOX模型风险评估结果不同于RBCA和CLEA模型的重要因素,3个模型间参数取值及方法学的差异也会导致风险评估结果不同.各模型暴     

天津地区大气污染状况和气溶胶硫酸盐的研究

我们于1980—1981年对天津市大气污染物浓度做了同步监测,对天津市大气污染状况,二氧化硫转化为硫酸盐的过程及其对大气能见度的影响做了研究。以超C_i几率和的方法处理数据,研究结果表明,大气污染以早晨最严重,傍晚次之,中午较轻:冬季比夏季污染严重。各种污染物中以硫酸盐对大气能见度的影响最大,总颗粒物次之。当大气相对湿度大于70%时,对大气能见度的影响比较突出。颗粒物中的苯溶物对大气能见度有一定的影响。城市中相对湿度高时硫酸盐浓度大,可能是产生冬季烟雾事件的原因。下风方向的硫酸根浓度与二氧化硫浓度的比值和硫酸根含硫浓度与大气总硫浓度的比值均比上风方向相应的数值高,说明城市燃煤烟气是硫酸盐的来源。城市中硫酸根浓度与二氧化硫浓度的相关系数为0.77,硫酸根与颗粒物浓度的相关系数为0.95。在形成硫酸根的过程中二氧化硫浓度和颗粒物可能有贡献。以一维有源简化模式估算二氧化硫转化为硫酸根的速率常数,约为2.3±1.1%/hr,冬季约1.5%/hr。二氧化硫的迁移距离约为17—340km。     

组合阳极联合气体扩散阴极电催化降解苯胺

采用气体扩散电极为阴极,钛基氧化物（Ti／SnO2-Sb2O5-IrO2）和金属铁构成组合阳极,构建了新型电化学氧化体系用于降解有机污染物。利用该氧化体系,在不同实验条件下考察了苯胺降解的效果与降解过程的相关规律。结果表明,阴极电位、铁阳极通电时间以及苯胺初始浓度均显著影响苯胺的降解效果。当阴极电位为-0．7V,pH3．0,铁阳极通电时间20min时,电化学处理200mg／L苯胺480min,TOC的去除效率达到80．4％,矿化电流效率（MCE）为8．6％,显示了该氧化体系具有良好的有机物降解能力。此外,苯胺降解过程中氨氮和硝态氮浓度的变化表明,苯胺分子中的氮主要转化为NH4和NO3^-。     

污水厂污泥一体化竖式强化渗滤浓缩自然干化与消化研究

针对目前国内污泥处理处置存在的问题,为实现污泥浓缩消化一体化,开发了污泥一体化强化渗滤浓缩自然干化与消化新工艺反应器,并进行了城市水厂污泥处理试验.结果表明,在有机负荷为0.8 kg VSS/(m3·d)、平均水力停留时间为8.3 d、污泥停留时间为120 d的条件下,污泥有机物去除率可达到44.4%,排泥含水率达到79.1%,污泥消化与浓缩过程起到了相互促进的作用.渗滤液须抽回至污水处理厂处理.     

两相分配式生物反应器处理高盐废水中的苯酚

采用新型两相分配式生物反应器(TPPB)和前期研究得到的高效苯酚降解菌对高盐废水中苯酚的降解进行研究,研究中确定煤油为反应系统的最佳有机溶剂,并考察了废水苯酚含量、废水盐度以及搅拌器搅拌速度对苯酚降解的影响。结果表明,反应系统能正常降解苯酚含量为1 000～2 500 mg/L的高盐苯酚废水;反应系统在含盐量为100 g NaCl/L、搅拌速度为50 r/min的运行工况条件下,降解时间缩短为52 h,总酚去除率为20.58 mg/(L.h)。     

新疆油田高含硫化氢区块污染防治措施研究

针对车89井区的高含硫问题,新疆油田研究出化学除硫、负压闪蒸除硫和催化曝气除硫技术以及相关的配套工艺,并成功进行了现场试验;同时,为杜绝在车89井区环境敏感区域内污染事故的发生,新疆油田加大内外环保宣传软硬件建设力度,并依据专业评价实施了一系列防控管理措施,达到了预防在先、技术在先、管理在先的工作目标。     

环境影响评价中的公众参与机制研究

通过梳理分析环境影响评价相关法中公众参与的规定,对照UNEP有效的公众参与五要素,剖析环境影响评价中公众参与机制的不足,并提出完善环境影响评价中公众参与机制的对策。     

电解锰渣无害化处理技术

电解锰渣是湿法电解金属锰工艺产生的废渣,环境危害性大、治理难度大。为消除锰渣的污染性,实验研究了锰渣浸出液中污染物种类,并分别采用生石灰和氢氧化钠作处理剂,从成本、处理效果方面进行比较,确定处理剂以及最佳运行条件。得出结论：锰渣中主要污染物为锰和氨氮（分别超过相关标准453倍和26倍）,选取生石灰做处理剂,处理后的锰渣,浸出液中锰离子和氨氮的减排量分别达到99%和97%以上,水溶性锰离子浓度低于5 mg/L、氨氮浓度低于25 mg/L,均达到《污水综合排放标准》（GB8978-1996）中的排放标准;反应时间30 h以上、避免雨淋、不通风、无日照为最佳反应条件。