水源水生物处理系统启动与再启动过程的硝化性能

基于中试规模试验 ,考察了微污染水源水生物接触氧化处理系统启动与再启动过程的硝化性能 ,探讨了处理系统启动过程的影响因素 ,比较了启动与再启动过程的氨氮去除效果。研究结果表明 ,氨氮去除量上升速率近似反映了启动与再启动过程硝化细菌的对数增长速率 ,是启动与再启动进程的重要量度 ;水温影响启动与再启动过程所需的时间 ,气水比影响处理系统可达到的氨氮硝化能力 ;保持长有成熟生物膜的填料浸没于水中 ,再启动过程较新填料挂膜的启动过程硝化细菌适应期短。     

城市环境空气中颗粒物源解析研究

颗粒物是我国大多数城市环境空气中的首要污染物.由于缺乏对颗粒物成分及来源的研究,导致目前的控制措施常常缺乏针对性.为全面弄清城市环境空气中颗粒物的来源,分采暖期和非采暖期对城市的主要大气污染源进行识别和采样,包括煤烟尘、建筑水泥尘、扬尘、土壤风沙尘、海盐粒子和二次粒子,并利用原子发射光谱、离子色谱等仪器对其成分进行定性定量分析,建立可吸入颗粒物的源成分谱.从而得出颗粒物元素成分谱,通过化学质量平衡(CMB)受体模型进行解析,得出各污染源对受体的贡献值和分担率.确定主要污染源,为采取针对性的措施治理污染提供依据.     

经济手段对环境保护的作用

经济手段对环境保护的作用王奇,李庆伦（沈阳市环境保护投资公司沈阳１１０００３）（东北大学表面所）ＩＭＰＲＯＶＩＮＧＴＨＥＴＲＥＡＴＭＥＮＴＥＦＦＣＴＯＦＷＡＳＴＥＷＡＴＥＲＣＯＮＴＡＩＮＩＮＧＬＥＡＤＡＮＤＡＣＩＤＢＹＳＣＩＥＮＴＩＦＩＣＭＡＮＡＧＥ...     

南京市大气气溶胶中颗粒物和正构烷烃特征及来源分析

于2002年夏季（7月）和冬季（12月）采集南京市5个功能区的大气气溶胶（PM2．5和PM10）样品，对两个季节不同功能区颗粒物及其颗粒物中正构烷烃的分布特征和污染来源进行了分析。结果表明，南京市大气颗粒物含量冬季高于夏季，细颗粒高于粗颗粒。正构烷烃的变化规律同颗粒物一致，且主要分布在细颗粒物上。根据各个功能区正构烷烃（C15-C32）的CPI（CPI1、CPI2和CPI3）结果，可知南京市大气气溶胶中正构烷烃由生物源和人为源共同排放产生。％waxCn的结果表明生物源对气溶胶中正构烷烃的贡献率为20％～43％，对南京市大气颗粒物的贡献率为1．66％～4．76％。     

Sources of organic aerosol: Positive matrix factorization of molecular marker data and comparison of results from different source apportionment models

This paper presents results from positive matrix factorization (PMF) of organic molecular marker data to investigate the sources of organic carbon (OC) in Pittsburgh, Pennsylvania. PMF analysis of 21 different combinations of input species found essentially the same seven factors with distinctive source-class-specific groupings of molecular markers. To link factors with source classes we directly compare PMF factor profiles with actual source profiles. Six of the PMF factors appear related to primary emissions from sources such as motor vehicles, biomass combustion, and food cooking. Each primary factor contributed between 5% and 10% of the annual-average OC with the exception of the cooking related factor which contributed 20% of the OC. However, the contribution of the cooking factor was sensitive to the specific combinations of input species. PMF could not differentiate between gasoline and diesel emissions, but the aggregate contribution of primary emissions from these two source classes is estimated to be less than 10% of the annual-average OC. One factor appears related to secondary organic aerosol based on its substantial contribution to biogenic oxidation products. This secondary factor contributed more than 50% of the summertime average OC. Reasonable agreement was observed between the PMF results and those of a previously published chemical mass balance (CMB) analysis of the same molecular marker dataset. Individual PMF factors are correlated with specific CMB sources, but systematic biases exist between the two estimates. These biases were generally within the uncertainty of the two estimates, but there is also evidence that PMF is not cleanly differentiating between source classes.     

Spatiotemporal variations of nitrate sources and dynamics in a typical agricultural riverine system under monsoon climate

Nitrogen pollution is a serious environmental issue in the Danjiangkou Reservoir region (DRR), the water source of the South-to-North Water Diversion Project of China. In this research, seasonal surveys and a bi-weekly time series survey were conducted in the Qihe River Basin, one of the most densely populated agricultural basins in the DRR. Hydrochemical compositions (NO₃^? and Cl^?), dual isotopes (δD-H₂O, δ¹⁸O-H₂O, δ¹⁵N-NO₃^?, and δ¹⁸O-NO₃^?), and a Markov Chain Monte Carlo isotope mixing model were jointly applied to unravel the sources, migrations, and transformations of the nitrate (NO₃^?) in the basin. It was revealed that the mixing between different sources was the main process controlling the isotopic compositions of the riverine NO₃^? in the upper-middle reaches. In contrast, denitrification occurred in the lower reaches. For the first time, the sources of NO₃^? were quantified at a basin scale in the DRR. Overall, the river transported 484.2 tons/year of NO₃-N to the reservoir, of which 32.6%, 36.4%, 28.0%, and 3.0% was from soil organic nitrogen, chemical fertilizer, residential sewage and atmospheric precipitation, respectively. The NO₃-N fluxes of the different sources were regulated by the monsoon climate and anthropogenic activities. For example, high precipitation and intense fertilization resulted in severe nonpoint source pollution. Denitrification thrived in soils and reservoirs in wet seasons. Temperature could regulate the migration, nitrification and denitrification processes. Based on the results, we suggest that the management strategies dealing with nitrogen pollution issue in the DRR should follow the specific spatiotemporal characteristics of NO₃^? sources, migration and transformation mechanisms.     

Chemical characteristics and sources of water-soluble organic aerosol in southwest suburb of Beijing

PM_2.5 filter sampling and components measurement were conducted in autumn and winter from 2014 to 2015 at a suburban site (referred herein as “LLH site”) located in the southwest of Beijing. The offline aerosol mass spectrometry (offline-AMS) analysis and positive matrix factorization (PMF) were applied for measurement and source apportionment of water-soluble organic aerosol (WSOA). Organic aerosol (OA) always dominated PM_2.5 during the sampling period, especially in winter. WSOA pollution was serious during the polluted period both in autumn (31.1 µg/m³) and winter (31.9 µg/m³), while WSOA accounted for 54.4% of OA during the polluted period in autumn, much more than that (21.3%) in winter. The oxidation degree of WSOA at LLH site was at a high level (oxygen-to-carbon ratio, O/C=0.91) and secondary organic aerosol (SOA) contributed more mass ratio of WSOA than primary organic aerosol (POA) during the whole observation period. In winter, coal combustion OA (CCOA) was a stable source of OA and on average accounted for 25.1% of WSOA. In autumn, biomass burning OA (BBOA) from household combustion contributed 38.3% of WSOA during polluted period. In addition to oxygenated OA (OOA), aqueous-oxygenated OA (aq-OOA) was identified as an important factor of SOA. During heavy pollution period, the mass proportion of aq-OOA to WSOA increased significantly, implying the significant SOA formation through aqueous-phase process. The result of this study highlights the concentration on controlling the residential coal and biomass burning, as well as the research needs on aqueous chemistry in OA formation.     

Temporal variations and source apportionment of volatile organic compounds at an urban site in Shijiazhuang, China

Shijiazhuang, the city with the worst air quality in China, is suffering from severe ozone pollution in summer. As the key precursors of ozone generation, it is necessary to control the Volatile Organic Compounds (VOCs) pollution. To have a better understanding of the pollution status and source contribution, the concentrations of 117 ambient VOCs were analyzed from April to August 2018 in an urban site in Shijiazhuang. Results showed that the monthly average concentration of total VOCs was 66.27 ppbv, in which, the oxygenated VOCs (37.89%), alkanes (33.89%), and halogenated hydrocarbons (13.31%) were the main composite on. Eight major sources were identified using Positive Matrix Factorization modeling with an accurate VOCs emission inventory as inter-complementary methods revealed that the petrochemical industry (26.24%), other industrial sources (15.19%), and traffic source (12.24%) were the major sources for ambient VOCs in Shijiazhuang. The spatial distributions of major industrial activities emissions were identified by using geographic information statistics system, which illustrated the VOCs was mainly from the north and southeast of Shijiazhuang. The inverse trajectory analysis using Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) and Potential Source Contribution Function (PSCF) clearly demonstrated the features of pollutant transport to Shijiazhuang. These findings can provide references for local governments regarding control strategies to reduce VOCs emissions.     

The pollution levels, variation characteristics, sources and implications of atmospheric carbonyls in a typical rural area of North China Plain during winter

Atmospheric carbonyls were measured at a typical rural area of the North China Plain (NCP) from November 13 to December 24, 2017 to investigate the pollution characteristics, sources and environmental implications. Fifteen carbonyls were detected, and formaldehyde, acetaldehyde and acetone accounted for about 81% at most. The concentration of the total carbonyls in heavily polluted days was twice more than that in clean days. In contrast to other carbonyls, m-tolualdehyde exhibited relatively high concentrations in the clean days in comparison with the polluted days. The ratios of three principal carbonyls to CO showed similar daily variations at different pollution levels with significant daytime peaks. Multiple linear regression analysis revealed that the contributions of background, primary and secondary sources to three principal carbonyls showed similar variation trends from the clean level to the heavily polluted level. The OH formation rate of formaldehyde showed a similar variation trend to its photodegradation rate, reaching the peak value at noon, which is important to maintain relatively high OH levels to initiate the oxidation of various gas-phase pollutants for secondary pollutant formation at the rural site. OH radical consumption rate and ozone formation potential (OFP) calculations showed that formaldehyde and acetaldehyde were the dominant oxidative species among measured carbonyls. As for OH radical consumption, n-butyraldehyde and m-tolualdehyde were important contributors, while for ozone formation potential, n-butyraldehyde and propionaldehyde made significant contributions. In addition, the contribution of carbonyl compounds to secondary organic aerosol (SOA) formation was also important and needs further investigation.     

Characteristics of atmospheric volatile organic compounds in urban area of Beijing: Variations, photochemical reactivity and source apportionment

Atmospheric volatile organic compounds (VOCs) were observed by an on-line gas chromatography-flame ionization detector monitoring system from November 2016 to August 2017 in Beijing. The average concentrations were winter (40.27 ± 25.25 μg/m³) > autumn (34.25 ± 19.90 µg/m³) > summer (32.53 ± 17.39 µg/m³) > spring (24.72 ± 17.22 µg/m³). Although benzene (15.70%), propane (11.02%), ethane (9.32%) and n-butane (6.77%) were the most abundant species, ethylene (14.07%) and propene (11.20%) were the key reactive species to ozone formation potential (OFP), and benzene, toluene, ethylbenzene, m-xylene + p-xylene and o-xylene (54.13%) were the most reactive species to secondary organic aerosol formation potential (SOAFP). The diurnal and seasonal variations indicated that diesel vehicle emission during early morning, gasoline vehicle emission at the traffic rush hours and coal burning during the heating period might be important sources. Five major sources were further identified by positive matrix factorization (PMF). The vehicle exhaust (gasoline exhaust and diesel exhaust) was found to be contributed most to atmospheric VOCs, with 43.59%, 41.91%, 50.45% and 43.91%, respectively in spring, summer, autumn and winter; while solvent usage contributed least, with 11.10%, 7.13%, 14.00% and 19.87%, respectively. Biogenic emission sources (13.11%) were only identified in summer. However, both vehicle exhaust and solvent usage were identified to be the key sources considering contributions to the OFP and SOAFP. Besides, the contributions of combustion during heating period and gasoline evaporation source during warm seasons to OFP and SOAFP should not be overlooked.