大气环境数值模拟在煤炭矿区规划环评中的应用研究

为解决煤炭矿区的区域性复合型大气污染问题和探讨煤炭矿区规划的大气环境影响评价技术方法,本文以山西省阳泉矿区为例,通过对比不同模型,选用CALPUFF模型模拟了2013年阳泉矿区及周边地区的大气污染特征,分析污染物超标原因并优化了污染源布局,最后对远期规划实施后不同布局下的环境质量进行预测对比.结果表明,CALPUFF模型可应用于煤炭矿区大气环境质量模拟,矿区总体规划实施以来,研究区内的PM10和N02浓度均达国家二级标准,但是部分地区的SO2浓度超标.通过优化布局可有效提高环境质量,使得现状及远期规划实施完成后的常规污染物年均浓度值均稳定满足国家二级标准.     

大气降水中重金属离子特征研究

大气降水中重金属离子的研究可以反映大气污染、地表水污染的信息.通过对国内外大气降水中重金属研究现状的阐述和大气降水中重金属的来源进行理论分析,并利用实地大气降水采样分析,归纳出其中重金属的特征,监测当前大气的污染状况,从而为区域性的大气中重金属的污染评价及污染治理提供理论依据.降水中的重金属元素主要包括Pb、Mn、Zn、Cu、Cd、Cr等,通过分析测定可以为利用大气降水作为重要饮用水补给源的区域提供饮水安全保障.     

“十一五”期间太原市环境空气质量及影响因素分析研究

依据太原市环境空气质量监测数据,采用Daniel趋势检验法,综合污染指数法和回归分析法研究了“十一五”期间太原市的环境质量变化趋势和影响因素.结果表明,从年均浓度值分析来看,除NO2外,SO2和PM10都存在超标现象,长期来看,三种污染物浓度下降趋势明显,这与太原市环境保护行动密切相关.月际间浓度值差异除PM10在春季出现波动外,SO2和NO2均呈现“U”型曲线,这种规律与气象条件密切相关.三种主要大气污染物污染指数都有所下降,但太原市区空气污染仍以SO2和PM10为主,说明烟煤型污染的空气污染特征没有改变.主要大气污染物的空间浓度分布不均与地形和气象特征以及城市布局和污染源排放有直接关系.太原市“十一五”期间大气环境质量整体改善,但形势依然严峻.     

西安市PM_(2.5)污染源位置确定的模型应用研究

针对空气中PM2.5污染物的传播问题,以西安市的情况为实例,合理考虑风力等天气和季节因素的影响,建立能够刻画该地区PM2.5的发生和演变规律的有风高斯点源扩散数学模型,代入相关数据后,利用MATLAB软件求解出PM2.5污染源由一区扩散到另一区的浓度,最后由综合的各区总浓度得出PM2.5污染源的位置,并与该市实际检测到PM2.5数据进行对比分析。结果表明,确定的位置比较准确,该方法能为城市污染治理提供参考。     

Pd/activated carbon sorbents for mid-temperature capture of mercury from coal-derived fuel gas

Higher concentrations of Hg can be emitted from coal pyrolysis or gasification than from coal combustion, especially elemental Hg. Highly efficient Hg removal technology from coal-derived fuel gas is thus of great importance. Based on the very excellent Hg removal ability of Pd and the high adsorption abilities of activated carbon（AC） for H2 S and Hg, a series of Pd/AC sorbents was prepared by using pore volume impregnation, and their performance in capturing Hg and H2 S from coal-derived fuel gas was investigated using a laboratory-scale fixed-bed reactor. The effects of loading amount, reaction temperature and reaction atmosphere on Hg removal from coal-derived fuel gas were studied. The sorbents were characterized by N2 adsorption, X-ray diffraction（XRD） and X-ray photoelectron spectroscopy（XPS）. The results indicated that the efficiency of Hg removal increased with the increasing of Pd loading amount, but the effective utilization rate of the active component Pd decreased significantly at the same time. High temperature had a negative influence on the Hg removal. The efficiency of Hg removal in the N2-H2S-H2-CO-Hg atmosphere（simulated coal gas） was higher than that in N2-H2S-Hg and N2-Hg atmospheres, which showed that H2 and CO, with their reducing capacity, could benefit promote the removal of Hg. The XPS results suggested that there were two different ways of capturing Hg over sorbents in N2-H2S-Hg and N2-Hg atmospheres.     

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.     

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.     

近10 a来珠江三角洲地区氮收支演变及区域差异分析

采用2000、2005 和2010 年三个不同时期的工业、农业、环保、自然条件和人口等相关数据,通过大量数理统计分析对近10 a 来珠江三角洲（简称“珠三角”）地区的氮收支演变与区域差异进行了评估。结果表明,在过去三个不同时期,珠三角地区氮的年输入、输出量有升有降,但是氮盈余总量却呈现出较显著的增加趋势,单位面积氮盈余量也从2000 年的43.43 kg/（hm²·a）增加到2010 年的51.92 kg/（hm²·a）。整个珠三角地区的负荷氮水平较全国平均水平偏高,但尚低于同样经济发展迅速、人口密集的长江三角洲地区的平均水平。快速的城市化发展和日益增强的人类活动对珠三角地区氮收支变化具有较大影响,且表现出非常显著的内部区域差异,深圳、东莞、佛山和广州等城市均面临较为严峻的氮污染潜势。     

挥发性有机污染物排放控制标准体系的建立与完善

以大气灰霾为代表的区域复合污染问题,导致挥发性有机物(VOCs)成为重点控制的污染物之一.通过对国家和地方挥发性有机污染物排放标准现状分析,依据排放特征以及我国挥发性有机物排放清单,建立和完善挥发性有机物排放控制标准体系.