日本森林大气中过氧化物的浓度及其对森林植物的影响

为了研究森林衰退的原因,于2000,2001和2002年的8月,分别选择出现森林衰退的日本奥日光白根山落叶树森林和未出现森林衰退的长野县大芝高原红松森林设立监测点,对光化学氧化剂臭氧(O3)和过氧化物的浓度进行监测,同时利用人工气候室对森林植物山毛榉和白桦进行了50′10-9O3、100′10-9O3和50′10-9O3+2′10-9~3′10-9过氧化物(过氧化氢(H2O2)及甲基过氧化氢(MHP))的暴露实验.野外监测结果表明,监测期间奥日光和长野的O3平均浓度相同,奥日光的H2O2及MHP平均浓度均高于长野;大气中的H2O2和MHP总是与O3共存,并且其浓度随O3浓度的增加而增加.暴露实验结果表明,暴露于50′10-9O3+2′10-9~3′10-9过氧化物的山毛榉和白桦出现了不同于O3暴露的叶片伤害症状;与100′10-9O3相比,50′10-9O3+2′10-9~3′10-9过氧化物导致植物出现了严重的叶片伤害和显著的光合速率下降.研究结果表明,除O3外,大气中的过氧化物也是导致森林衰退的原因之一.     

钢铁行业大气环境影响评价方法与建议

按钢铁行业大气环评报告书的结构和顺序,结合HJ 2.2-2008《环境影响评价技术导则大气环境》中的相关技术要求,从评价因子、源强、评价等级、大气监测、大气预测、防护距离等方面出发,分析了钢铁行业大气环评中的评价等级确定、大气监测、大气预测等工作中存在的问题,并提出解决方案和建议对策。     

Potential particulate pollution derived from UV-induced degradation of odorous dimethyl sulfide

UV-induced degradation of odorous dimethyl sulfide (DMS) was carried out in a static White cell chamber with UV irradiation. The combination of in situ Fourier transform infrared (FT-IR) spectrometer, gas chromatograph-mass spectrometer (GC-MS), wide-range particle spectrometer (WPS) technique, filter sampling and ion chromatographic (IC) analysis was used to monitor the gaseous and potential particulate products. During 240 min of UV irradiation, the degradation e ciency of DMS attained 20.9%, and partially oxidized sulfur-containing gaseous products, such as sulfur dioxide (SO2), carbonyl sulfide (OCS), dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO2) and dimethyl disulfide (DMDS) were identified by in situ FT-IR and GC-MS analysis, respectively. Accompanying with the oxidation of DMS, suspended particles were directly detected to be formed by WPS techniques. These particles were measured mainly in the size range of accumulation mode, and increased their count median diameter throughout the whole removal process. IC analysis of the filter samples revealed that methanesulfonic acid (MSA), sulfuric acid (H2SO4) and other unidentified chemicals accounted for the major non-refractory compositions of these particles. Based on products analysis and possible intermediates formed, the degradation pathways of DMS were proposed as the combination of the O(1D)- and the OH- initiated oxidation mechanisms. A plausible formation mechanism of the suspended particles was also analyzed. It is concluded that UV-induced degradation of odorous DMS is potentially a source of particulate pollutants in the atmosphere.     

Experimental study on filtration and continuous regeneration of a particulate filter system for heavy-duty diesel engines

This study investigated the filtration and continuous regeneration of a particulate filter system on an engine test bench, consisting of a diesel oxidation catalyst（DOC） and a catalyzed diesel particulate filter（CDPF）. Both the DOC and the CDPF led to a high conversion of NO to NO2 for continuous regeneration. The filtration efficiency on solid particle number（SPN） was close to100%. The post-CDPF particles were mainly in accumulation mode. The downstream SPN was sensitively influenced by the variation of the soot loading. This phenomenon provides a method for determining the balance point temperature by measuring the trend of SPN concentration.     

Seasonal and diurnal variations of atmospheric peroxyacetyl nitrate, peroxypropionyl nitrate, and carbon tetrachloride in Beijing

Atmospheric peroxyacetyl nitrate(PAN), peroxypropionyl nitrate(PPN), and carbon tetrachloride(CCl4) were measured from September 2010 to August 2011 in Beijing. PAN exhibited low values from mid-autumn to early spring(October to March) with monthly average concentrations ranging from 0.28 to 0.73 ppbV, and increased from early spring to summer(March to August), ranging from 1.37–3.79 ppbV. The monthly variation of PPN was similar to PAN, with low values(below detection limit to 0.18 ppbV) from mid-autumn to early spring, and a monthly maximum in September(1.14 ppbV). The monthly variation of CCl4was tightly related to the variation of temperature, exhibiting a minimum in winter(69.3 pptV) and a maximum of 180.6 pptV in summer. Due to weak solar intensity and short duration, PAN and O3showed no distinct diurnal patterns from morning to night during winter, whereas for other seasons, they both exhibited maximal values in the late afternoon(ca. 15:00 to 16:00 local time) and minimal values during early morning and midnight. Good linear correlations between PAN and PPN were found in autumn(R = 0.91), spring(R = 0.94), and summer(R = 0.81), with slopes of 0.130, 0.222, and 0.133, respectively, suggesting that anthropogenic hydrocarbons dominated the photochemical formation of PANs in Beijing. Positive correlation between PAN and O3 in summer with the low slopes( O3 / PAN) ranging from 9.92 to 18.0 indicated serious air pollution in Beijing, and strong negative correlation in winter reflected strong O3consumption by NO titration and less thermal decompositin of PAN.     

Characteristics of atmospheric particles and heavy metals in winter in Chang-Zhu-Tan city clusters, China

To understand the pollution characteristics of atmospheric particles and heavy metals in winter in Chang-Zhu-Tan city clusters, China, total suspended particulate(TSP) and PM10samples were collected in cities of Changsha, Zhuzhou and Xiangtan from December 2011 to January 2012, and heavy metals of Cd, Pb, Cr, and As were analyzed. It shows that the average TSP concentration in Changsha, Zhuzhou and Xiangtan were(183 ± 73),(201 ± 84) and(190 ± 66) μg/m3respectively, and the average PM10 were(171 ± 82),(178 ± 65) and(179 ± 55) μg/m3respectively. The lowest TSP and PM10concentrations occurred at the background Shaping site of Changsha. The average ratio of ρ(PM10)/ρ(TSP) was 91.9%, ranging from 81.3% to 98.9%. Concerning heavy metals, in TSP samples, the concentration of Cr, As, Cd and Pb were 28.8–56.5, 18.1–76.3, 3.9–26.1 and 148.0–460.9 ng/m3, respectively, while in PM10samples, were 16.4–42.1, 15.5–67.9, 3.3–22.2 and 127.9–389.3 ng/m3, respectively. The enrichment factor of Cd was the highest, followed by Pb and As, while that of Cr was the lowest.     

北京市PM5.0可吸入颗粒物反演及其时空分布分析

分析城市可吸入颗粒物的空间特征及影响因素对于制定更为有效的可吸入颗粒物污染控制政策具有重要的现实意义.本研究在实际采样和遥感数据处理基础上,构造差值植被指数(DVI),通过建立TM影像与对应PM5.0颗粒物实测值之间的相关关系模型,对北京市2008~2010年3 a的PM5.0的分布进行了反演计算和精度分析;研究了NDBI和NDMI对PM5.0浓度的影响,进一步揭示了北京五环区域范围内可吸入颗粒物的时空分布特征.结果表明,采用DVI反演PM5.0分布的方法可行,反演精度在可接受范围内;整体上研究区2008年PM5.0颗粒物污染最轻,西南三环和四环以及东南三四环之间为颗粒物污染的高值区,西北五环附近颗粒物污染较轻;NDBI(归一化建筑指数)、NDMI(归一化水汽指数)与PM5.0可吸入颗粒物的分布分别呈现显著的负相关和正相关关系,且二者对PM5.0的影响相近.     

汉江上游金水河流域氮湿沉降

汉江上游金水河流域是南水北调工程的重要水源涵养区,但是氮污染已成为该流域水质的主要威胁因素.该研究对汉江的金水河流域开展了为期1 a(2012-02~2013-02)的氮湿沉降观测,并利用氮输出模型估算了氮湿沉降对河流氮负荷的贡献量.结果表明雨水中总氮(DTN)的浓度在0.24~2.89 mg·L-1之间,铵态氮(NH+4-N)、硝态氮(NO-3N)及有机氮(DON)分别占42.8%、13.3%和43.9%;雨水氮浓度随降雨量增大而变小,明显受到降雨的稀释作用.流域内氮湿沉降主要来自人类活动,沉降负荷在4.97~7.00 kg·(hm2·a)-1之间,受降雨量的主要影响,上游地区的氮湿沉降负荷>下游地区>中游地区,春夏两季约占全年氮湿沉降的81%.流域氮湿沉降对河流氮负荷贡献量约为34 000~46 000 kg,只占流域氮肥贡献量的5.05%~6.78%,远小于流域内农业活动化肥氮的贡献量,不是河流氮的主要来源.     

桂江主要离子及溶解无机碳的生物地球化学过程

河流水体的化学组成记录了流域内各种自然过程与人类活动的信息.对西江一级支流桂江化学径流的分析结果表明,桂江水体的离子组成主要受碳酸盐岩化学风化过程的控制,CO2是这一过程的主要侵蚀介质;H2SO4对碳酸盐岩的风化影响桂江河水的化学组成.大气沉降、人类活动、碳酸盐岩和硅酸盐岩化学风化对桂江水体贡献的溶解物质分别占总溶解物质的2.7%、6.3%、72.8%和18.2%.河流溶解无机碳(DIC)的稳定同位素组成(δ13CDIC)揭示桂江河水中的DIC明显被浮游植物的光合作用所利用.浮游植物初级生产力对桂江颗粒有机碳(POC)的贡献达22.3%~30.9%,这表明岩石风化来源的DIC经浮游植物的光合作用转化为有机碳,并在迁移过程中部分沉积水体底部,进而形成埋藏有机碳.     

焦炉排放多环芳烃与人体健康风险评价研究

焦炉炼焦产生多环芳烃物质(PAHs)具有较强毒性和致癌作用,本研究以某大型钢铁企业焦炉为例,采用AERMOD扩散模式来预测分析焦炉排放PAHs共13种污染物在大气中迁移扩散情况,采用BREEZE Risk Analyst根据人体健康风险评价导则HHRAP计算评价范围内受体人群PAHs污染物致癌和危害指数,对焦炉排放PAHs的健康风险进行了定量评价.结果表明,应重点关注焦炉排放萘危害指数值影响(最大值为0.97).焦炉排放各污染物单因子致癌风险均小于1.0E-06,而综合考虑多环芳烃总致癌风险值最大达到2.65E-06,对当地居民的人体健康可能存在一定的影响.