2013 — 2016年西安市臭氧时空变化特性与影响因素

臭氧污染主要是由前体物氮氧化物（NO_x）和挥发性有机物（VOC）的过量排放引起的,通过NO_x/?SO₂的比值可得知西安地区已经受到了光化学烟雾型污染的影响,大气中臭氧含量与NO_x的含量相关性较高;西安13个站点的8小时平均浓度分布变化大体可分为单峰变化和持续递减类型,浓度主要集中在0?—?90 μg???m^?3,不同站点臭氧含量相差较大;2013?—?2016年,高新西区臭氧超标天数最多,为146天,是超标天数最少的兴庆小区的2倍多。高浓度臭氧主要出现在高温度、低湿度、实时风向为东南风或南风的天气。此外,治理臭氧污染必须限制机动车尾气排放,同时研究表明来自秦岭的植物VOC对于西安臭氧浓度影响很大。     

土壤及土壤矿物对类胡敏酸的吸附解吸及其影响因素研究

应用平衡吸附法,研究了不同pH值、离子强度、类胡敏酸浓度和接触时间条件下,黑土、白浆土及蒙脱石对类胡敏酸(HLA)的吸附作用.结果表明:随着HLA浓度的增加,土壤及蒙脱石对HLA的吸附量增加.黑土、白浆土及蒙脱石对HLA的吸附等温线均为L型,其吸附不可逆性表现为白浆土＞蒙脱石＞黑土.通过Langmiur方程计算,蒙脱石、白浆土对HLA达到吸附平衡时的最大吸附量分别为764.7、790.3 mg·g-1,而黑土为35.27 mg·g-1.Freundlich方程可以很好地描述白浆土、蒙脱石对HLA的吸附和解吸等温线,而Temkin方程可以很好地描述黑土对HLA的吸附和解吸等温线.同时,3种材料的吸附自由能△G°＜0,吸附热Qm ＞0,表明其对HLA的吸附是自发的、放热的过程.随着pH的升高,黑土、白浆土及蒙脱石对HLA的吸附量减少;随离子强度的增加,黑土、白浆土及蒙脱石对HLA的吸附量增大.黑土、白浆土及蒙脱石对HLA的吸附动力学过程划分为快反应和慢反应阶段,其中,蒙脱石、白浆土对HLA的吸附动力学过程用一级动力学方程拟合的效果最好,而对黑土而言,用Elovich方程描述更合适.     

Factors influencing the contents of metals and As in soils around the watershed of Guanting Reservoir, China

Topsoil samples from 61 sites around the Guanting Reservoir,China,were measured for Cu,Zn,Cr,Ni,Cd,Pb and As concentrations.The mean concentrations of Cu,Zn,Cr,Ni,Cd,Pb and As were 16.8,59.4,37.8,18.3,0.32,20.1 and 8.67 mg/kg dry weight,respectively.Factors that influence the dynamics of these metals in soils around the watersheds of Beijing reservoirs were examined.The influence of atmospheric deposition,land use,soil texture,soil type and soil chemical parameters on metal contents in soils was investigated.Atmospheric deposition,land use and soil texture were the important factors affecting heavy metal residues.Soil type and soil chemical parameters were also involved in heavy metal retention in soils.The data provided in this study are considered crucial for reservoir remediation,especially since the Guanting Reservoir will serve as one of the main drinking water sources for Beijing in the foreseeable future.     

Sulfur-containing amino acid methionine as the precursor of volatile organic sulfur compounds in algea-induced black bloom

After the application of methionine, a progressive and significant increase occurred in five volatile organic sulfur compounds (VOSCs): methanethiol (MeSH), dimethyl sulfide (DMS), dimethyl disulfide (DMDS), dimethyl trisulfide (DMTS) and dimethyl tetrasulfide (DMTeS). Even in the untreated control without a methionine addition, methionine and its catabolites (VOSCs, mainly DMDS) were found in considerable amounts that were high enough to account for the water’s offensive odor. However, blackening only occurred in two methionine-amended treatments. The VOSCs production was observed to precede black color development, and the reaching of a peak value for total VOSCs was often followed by water blackening. The presence of glucose stimulated the degradation of methionine while postponing the occurrence of the black color and inhibiting the production of VOSCs. In addition, DMDS was found to be the most abundant species produced after the addition of methionine alone, and DMTeS appeared to be the most important compound produced after the addition of methionine+glucose. These results suggest that methionine acted as an important precursor of the VOSCs in lakes suffering from algea-induced black bloom. The existence of glucose may change the transformation pathway of methionine into VOSCs to form larger molecular weight compounds, such as DMTS and DMTeS.     

Competitive sorption between 17α-ethinyl estradiol and bisphenol A/4-n-nonylphenol by soils

The sorption of 17α-ethinyl estradiol(EE2),bisphenol A(BPA),and 4-n-nonylphenol(NP) in single systems and the sorption of EE2 with different initial aqueous concentrations of BPA or NP were examined using three soils.Results showed that all sorption isotherms were nonlinear and fit the Freundlich model.The degree of nonlinearity was in the order BPA(0.537-0.686) > EE2(0.705-0.858) > NP(0.875-0.0.951) in single systems.The isotherm linearity index of EE2 sorption calculated by the Freundlich model for Loam,Silt Loam and Silt increased from 0.758,0.705 and 0.858,to 0.889,0.910 and 0.969,respectively,when BPA concentration increased from 0 to 1000 μg/L,but the effect of NP was comparably minimal.Additionally,EE2 significantly suppressed the sorption of BPA,but insignificantly suppressed that of NP.These findings can be attributed to the difference of sorption affinity of EE2,NP and BPA on the hard carbon(e.g.,black carbon) of soil organic matter that dominated the sorption in the low equilibrium aqueous concentration range of endocrine-disrupting chemicals(EDCs).Competitive sorption among EDCs presents new challenges for predicting the transport and fate of EDCs under the influence of co-solutes.     

Multi-factors influencing the spatial distribution of polycyclic aromatic hydrocarbons in soils surrounding drinking water protection zone

We selected the Guanting Reservoir in Beijing, China as a case where an industrial area locates on the upwind corner to study the influence of human activities and natural processes on the distribution of polycyclic aromatic hydrocarbons (PAHs) in soils. Soil PAH concentrations in the study area follow a log-normal probability distribution function, suggesting that distribution of PAH in soils was affected by human activities. Distribution of PAHs in soils was significantly affected by the point source that high PAH concentrations were observed in near industrial area with an obvious declining trend from the northwest to the southeast which was the prevailing wind direction in this area. Away from the influence of point source, distribution of PAHs in soils was found to significantly correlate with total organic carbon content, while the influences of agricultural land uses and type of soil texture on the total soil PAHs contents and ring compositions were quite limited. The results can provide some evidences and data on the pollutant accumulation in drink water protection area influenced by natural processes and human activities.     

Electrochemical and spectroscopic characteristics of dissolved organic matter in a forest soil profile

Dissolved organic matter （DOM） represents one of the most mobile and reactive organic compounds in ecosystem and plays an important role in the fate and transport of soil organic pollutants, nutrient cycling and more importantly global climate change. Electrochemical methods were first employed to evaluate DOM redox properties, and spectroscopic approaches were utilized to obtain information concerning its composition and structure. DOM was extracted from a forest soil profile with five horizons. Differential pulse voltammetry indicated that there were more redox-active moieties in the DOM from upper horizons than in that from lower horizons. Cyclic voltammetry further showed that these moieties were reversible in electron transfer. Chronoamperometry was employed to quantify the electron transfer capacity of DOM, including electron acceptor capacity and electron donor capacity, both of which decreased sharply with increasing depth. FT-IR, UV-Vis and fluorescence spectra results suggested that DOM from the upper horizons was enriched with aromatic and humic structures while that from the lower horizons was rich in aliphatic carbon, which supported the findings obtained by electrochemical approaches. Electrochemical approaches combined with spectroscopic methods were applied to evaluate the characteristics of DOM extracted along a forest soil profile. The electrochemical properties of DOM, which can be rapidly and simply obtained, provide insight into the migration and transformation of DOM along a soil profile and will aid in better understanding of the biogeochemical role of DOM in natural environments.     

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.     

广州白云国际机场航空垃圾的处理及处置对策

广州白云国际机场是国家三大枢纽机场之一,随着广州白云国际机场航空事业的发展,航空垃圾的排放量越来越大,品种愈来愈多,对环境的影响也越来越明显。本文针对广州白云国际机场航空垃圾的产生情况、航空垃圾的处理现状进行分析,并对其将来航空垃圾的处理处置情况提出对策和建议。     

2种连续提取法提取3种类型土壤中重金属研究

连续提取法作为一种重要的化学分析方法,是土壤中重金属元素形态分析的主要环节,但不同提取法对于不同的土壤类型及同类土壤中不同重金属形态的提取效果差异很大.本文采用Tessier法和Maiz法等2种不同的连续提取法对华中地区常见的3种类型土壤(红壤、黄棕壤和黄褐土)中的Pb、Cd、Cu和Zn分别进行重金属形态分析,同时对Tessier法和Maiz法获得的结果进行了对比和分析.