基于循环特性的镍氢和锂离子电池环境影响机制分析

为了了解镍氢电池和锂离子电池在生产、使用、废弃或回收过程中的环境影响,建立了一种简单快速的二次电池环境影响机制分析方法。通过生命周期评价(LCA)方法,采用Eco-indicator99体系,综合考虑电池循环容量衰减和循环次数的影响,建立了二次电池环境影响机制分析模型,并运用此模型对两种实验用二次电池(镍氢电池和锂离子电池)的环境影响机制进行了研究。结果表明:1)在所选取的两种二次电池当中,锂离子(Li-ion)电池的环境影响明显比镍氢(Ni-MH)电池的低;2)随着循环次数的增加Li-ion电池环境影响衰减比Ni-MH电池的明显,即随着使用循环次数的增加,Li-ion电池对环境的影响会降低到更多。综合来说,所选取的Li-ion电池比Ni-MH电池更具环境可持续性。文中所提出的环境影响机制分析模型同样可以应用于其他二次电池,以期为环境友好型二次电池的开发提供帮助。     

第二松花江中下游水体邻苯二甲酸酯分布特征

通过采集和分析第二松花江中下游水和底泥样品,探讨了该河段水体中邻苯二甲酸酯(PAEs)含量及其分布特征。结果表明第二松花江中下游水体中PAEs以邻苯二甲酸二丁酯(DBP)和邻苯二甲酸双(2-乙基己基)酯(DEHP)两种为主。水中PAEs总量较高,DBP和DEHP含量均已超过我国地表水标准限值。底泥中PAEs总量与国内外一些河流底泥中的含量相近,但DBP和DEHP含量均已超过了美国华盛顿州的警戒标准。底泥中PAEs含量沿程分布总体上均呈现先增加后减少的特征;水体中PAEs含量及其分布特征主要受流域内工农业活动的影响。     

Changes in heavy metal contents in animal feeds and manures in an intensive animal production region of China

The 360 feed and manure samples were collected from 150 animal farms in Jiangsu Province, China and analyzed for heavy metals. Concentrations of Zn and Cu in animal feeds were 15.9-2041.8 and undetected-392.1 mg/kg respectively, while Hg, As, Pb, Cd, and Cr in all feeds were below 10 mg/kg. Concentrations of Cu, Zn, and Cr in animal manures were 8.4-1726, 39.5-11379, and 1.0-1602 mg/kg respectively, while As, Cd, Hg, and Pb were 〈 10 mg/kg. The concentration of Cu, Zn, As and Cr in animal feed and manure were positively correlated （p 〈 0.001）, but the Cd, Hg, and Pb were not statistically correlated between the feed and the manure. Concentrations of Cu and Zn were highest in pig feed and manure, followed by poultry and dairy feeds and manures. During 1990- 2008, Cu, Zn, As, Cr, Cd contents increased by 771%, 410%, 420%, 220%, and 63% in pig manure, 212%, 95%, 200%, 791%, and -63% in dairy manure, and 181%, 197%, 1500%, 261, and 196% in poultry manure. Most of the increases occurred from 2002 to 2008, which reflects the extensive use of feed additives after 2002. In contrast, Pb and Hg in manures continuously decreased from 1990 to 2008. The results suggest that the heavy metal contents in animal manure have been greatly increased over 18 years and the contribution of manures to soil should be considered.     

大气污染总量控制规划专家系统中知识库子系统的研究

论述了大气污染总量控制规划专家系统（ＥＡＳＰＴＥＣＥＰ）中知识库的基本设计思想,知识库分为无级知识库和领域级知识库,元级知识库由类文件和元规则文件构成,领域级知识库则文件和参量文件构成,并在此基础上阐述了ＥＳＡＰＴＥＣＰ中知识库演绎推理系统,知识库解释系统,知识库管理系统等的设计与实现方法。     

基于景观生态学的生态功能区划研究——以重庆市长寿区为例

针对目前生态功能区划仅从区域生态要素、生态敏感性与生态服务功能空间分异规律等方面考虑,而很少涉及景观格局特征与景观稳定度等景观生态学的内容;文章在景观生态学理论基础上,提出一套基于景观生态学的区域生态功能区划理论;一方面有助于生态功能小区的划分;另一方面可以弥补原有生态保育措施只考虑生态敏感性和生态服务功能重要性的不足,从景观生态学角度提出具有针对性的生态保育措施。文章将所建立的理论与方法用于重庆市长寿区生态功能区划,区划结果为:将重庆市长寿区划分为3个生态亚区,9个生态功能区和21个生态功能小区,与未考虑景观稳定度的生态功能区划相比,考虑景观稳定度的生态功能区划多了四个生态功能小区,而这四个生态功能小区的划出,有助于进一步针对具体问题,从生态学和景观生态学的角度提出生态保育措施,对重庆市长寿区环境保护和生态建设具有重要的指导意义。     

污水生物处理实际工艺中氧化亚氮的释放：现状与挑战

介绍了污水生物处理过程中N2O的产生途径,重点分析了污水厂典型脱氮工艺的N2O释放差异及其原因,提出了城市污水脱氮处理过程N2O减排的具体措施,并估算出全国城镇污水处理厂2011年N2O释放总量约为1.26×109g(以N计),对今后关于城市污水脱氮处理过程N2O产生及减排的研究趋势进行了评估.     

溶解性有机质对罗红霉素光降解的影响研究

近年来,罗红霉素(ROX)因其用量大、检出频率高和生态风险大引起了广泛关注.本文主要研究了环境pH条件下不同的溶解性有机质(DOM),包括富里酸(PLFA)、腐殖酸(SRHA)和天然有机质(SRNOM)对罗红霉素光降解的影响及主要活性物种对其光降解的贡献.结果表明:纯水中罗红霉素可发生自敏化光降解,在pH 6～8条件下,罗红霉素光降解的一级反应速率常数为0.0033～0.0049 h~(-1).DOM促进了罗红霉素光降解,其促进效果从大到小为PLFASRNOMSRHA.DOM共存时罗红霉素光降解的反应速率常数随pH增加而增加,在pH 6时为0.0145～0.0266 h~(-1),在pH 8时为0.0273～0.0577 h~(-1).通过异丙醇淬灭实验发现,羟基自由基(·OH)对罗红霉素光降解起主要贡献,其贡献率在pH 6时为83.45%～98.70%,在pH 8时降低至76.76%～78.02%;3种DOM体系中产生的单态氧(~1O_2)的稳态浓度在(5.15～7.86)×10~(-14) mol·L~(-1)范围内;在pH 6、7和8的条件下,~1O_2与罗红霉素的二级反应速率常数分别为2.27×10~5、1.96×10~6和1.51×10~7 L·mol~(-1)·s~(-1).~1O_2对罗红霉素的光降解的贡献随pH升高而升高,在pH 6时为0.21%～0.43%,在pH 8时为4.85%～11.33%.     

L-抗坏血酸还原降解六价铬的影响因素

对L-抗坏血酸(维生素C,VC)还原降解六价铬(Cr(Ⅵ))的影响因素进行了试验研究. 当ρ(VC)∶ρ(Cr(Ⅵ))为5∶1时,ρ(Cr(Ⅵ))降至检测限以下. 低温条件下仍能取得较高的Cr(Ⅵ)去除率,当反应体系温度维持在35 ℃时,Cr(Ⅵ)的去除率达到95.5%. 在饱和溶解氧条件下,Cr(Ⅵ)的去除率仍能达到85.5%. 氧化还原体系中VC和零价铁同时作为电子供体,存在竞争关系. VC还原降解Cr(Ⅵ)的产物为三价铬(Cr(Ⅲ))和脱氢抗坏血酸,反应化学计量比(n(VC)∶n(Cr(Ⅵ)))为3∶2.      

An online monitoring system for atmospheric nitrous acid (HONO) based on stripping coil and ion chromatography

A new instrument for measuring atmospheric nitrous acid(HONO) was developed,consisting of a double-wall glass stripping coil sampler coupled with ion chromatography(SC-IC).SC-IC is featured by small size(50 × 35 × 25 cm) and modular construction,including three independent parts:the sampling unit,the transfer and supporting unit,and the detection unit.High collection efficiency(> 99%) was achieved with 25 μmol/L Na2CO3 as absorption solution even in the presence of highly acidic compounds.This instrument has a detection limit of 8 pptv at 15 min time resolution,with a measurement uncertainty of 7%.Potential interferences from NOx,NO2+SO2,NO2+VOCs,HONO+O3,HNO3,peroxyacetyl nitrite(PAN) and particle nitrite were quantified in laboratory studies and were found to be insignificant under typical atmospheric conditions.Within the framework of the 3C-STAR project,inter-comparison between the SC-IC and LOPAP(long path liquid absorption photometer) was conducted at a rural site in the Pearl River Delta.Good agreement was achieved between the two instruments over three weeks.Both instruments determined a clear diurnal profile of ambient HONO concentrations from 0.1 to 2.5 ppbv.However,deviations were found for low ambient HONO concentrations(i.e.< 0.3 ppbv),which cannot be explained by previous investigated interference species.To accurately determine the HONO budget under illuminated conditions,more intercomparison of HONO measurement techniques is still needed in future studies,especially at low HONO concentrations.     

石油化工行业特征挥发性有机物主要成分研究

2014年青奥会期间,南京市采用苏玛罐采样和GC-MS分析的方法对2家石油化工企业部分典型工艺的特征挥发性有机物进行监测分析.结果表明:石油化工行业挥发性有机物主要组分为烷烃、苯系物、含氧有机物、卤代烃和烯烃;主要特征污染物包括异丁烷、正戊烷、正丁烷、正己烷、正庚烷、正辛烷、苯、甲苯、二甲苯、甲醇、乙醛、丙酮、二氯乙烷、三氯苯等.对石油化工行业挥发性有机物主要成分分析,为“十三五”开展的石油化工行业自行监测和环境管理提供了基础资料.