大气颗粒物中类腐殖酸的研究进展

类腐殖酸(HULIS)是一类广泛存在于云、雾、雨水和大气气溶胶颗粒中的大分子有机物.HULIS既可通过吸收和散射太阳辐射直接影响大气热平衡,又能参与云凝结核的形成间接影响全球气候,加之其重要的环境和健康效应,近年来引起科学界的广泛关注.本文综述了大气颗粒物中类腐殖酸的研究成果,主要包括HULIS的分离、提取和分析方法,HULIS的主要理化性质、浓度和季节变化,以及HULIS的来源和国内外研究现状,并对该领域的研究前景进行了分析和展望.     

Air pollution characteristics and their relationship with emissions and meteorology in the Yangtze River Delta region during 2014–2016

With rapid economic growth and urbanization, the Yangtze River Delta(YRD) region in China has experienced serious air pollution challenges. In this study, we analyzed the air pollution characteristics and their relationship with emissions and meteorology in the YRD region during 2014–2016. In recent years, the concentrations of all air pollutants, except O_3,decreased. Spatially, the PM_(2.5), PM_(10), SO_2, and CO concentrations were higher in the northern YRD region, and NO_2 and O_3 were higher in the central YRD region. Based on the number of non-attainment days(i.e., days with air quality index greater than 100), PM_(2.5) was the largest contributor to air pollution in the YRD region, followed by O_3, PM_(10), and NO_2.However, particulate matter pollution has declined gradually, while O_3 pollution worsened.Meteorological conditions mainly influenced day-to-day variations in pollutant concentrations. PM_(2.5) concentration was inversely related to wind speed, while O_3 concentration was positively correlated with temperature and negatively correlated with relative humidity.The air quality improvement in recent years was mainly attributed to emission reductions.During 2014–2016, PM_(2.5), PM_(10), SO_2, NO_x, CO, NH_3, and volatile organic compound(VOC)emissions in the YRD region were reduced by 26.3%, 29.2%, 32.4%, 8.1%, 15.9%, 4.5%, and0.3%, respectively. Regional transport also contributed to the air pollution. During regional haze periods, pollutants from North China and East China aggravated the pollution in the YRD region. Our findings suggest that emission reduction and regional joint prevention and control helped to improve the air quality in the YRD region.     

Polycyclic aromatic hydrocarbons (PAHs) in the aerosol in Beijing, China, measured by aminopropylsilane chemically-bonded stationary-phase column chromatography and HPLC/fluorescence detection

We developed a useful analytical method for the determination of polycyclic aromatic hydrocarbons (PAH) concentrations in the aerosol of China. We used an accelerated solvent extraction (ASE) method for the extraction of PAHs from the aerosol samples, in order to reduce the extraction time and the solvent volume used. The optimum purification method was developed, with aminopropylsilane chemically-bonded stationary-phase column chromatography, in order to remove many co-extractives which cannot be removed by conventional purification methods using silica-gel column chromatography. HPLC/fluorescence detection (FLD) was adopted as the analytical method, because it has very high sensitivity to PAH and it is easy to install, operate, and maintain as compared with GC/MS. With the analytical method developed in this study, the recovery and precision (RSD) for most of the PAHs ranged from 75% to 129% and from 2.8% to 22.7%, respectively. The concentrations of PAHs in the aerosol samples collected from October 2003 to April 2005 in Beijing, China were determined using the newly developed method. SigmaPAHs, which is the sum of the concentrations of all detected PAHs, was 177.8 +/- 239.9 ng m(-3) (n = 64). The SigmaPAHs concentration in the heating season (305.1 +/- 279.0 ng m(-3), n = 33) was 7.2 times higher than that in the non-heating season (42.3 +/- 32.0 ng m(-3), n = 31). These strong seasonal variations in atmospheric PAH concentration are possibly due to coal combustion for residential heating in winter.     

中国生态环境保护管理体制改革思路与方向:国际社会的观察和建议

本文对2000年以来国际组织和研究机构针对中国生态环境保护管理体制改革的研究进行了梳理和分析,总结了这些研究中提出的现行生态环境保护管理体制存在的主要问题,以及对于中国生态环境保护管理体制改革思路和方向的政策建议。本文对已实现的建议进行了分析,提出了未来生态环境保护管理体制改革亟待解决的问题。     

氧化镁FGD脱硫过程的建模及其应用

氧化镁烟气脱硫是以氧化镁为脱硫反应剂的一种湿法烟气脱硫技术，目前国内外应用甚少，但开发前景广阔。以实验室小试为基础，从气液传质入手，利用双膜理论建立脱硫过程的数学模型，从而对中试脱硫效率进行预测并进行参数敏感性分析。结果表明，模型预测的脱硫效率与实际脱硫效率有很高的吻合度，其计算参数能反映出实际运行参数对脱硫效率的影响，对实际工况中操作条件的变更以及运行参数的调试有很高的指导意义。     

生物质型煤成型技术开发实验研究

通过原有成型方式的工业成型观察和模压成型实验，提出并验证了完全利用生物质纤维的交联作用实现成型的新机制。其于中高压下物料的不可再压缩性和单向挤压也会导致更高的成型压力的新认识，设计和研制成按新机制成型的型轮。经此改进的工业成型试验达到了比模压成型更好的效果：不用预实送料，且成型性能；成型压力降至120MPa以下，成型许可水分成倍提高，适合的生物质配比范围15％－60％；仅利用送料螺旋的预实功能，即可实现纯生物质型块的成型。     

沈阳地区水环境和生物样品中全氟化合物的污染分布特征

采用高效液相色谱/电喷雾负电离源串联质谱法对沈阳市各类水环境和生物样品中全氟化合物(PFCs)进行测定,研究了PFCs的河流分布及季节分布特征.同时,对通过饮用水及家禽和鱼摄入全氟辛烷磺酸(PFOS)和全氟辛酸(PFOA)的人体健康风险进行了评价.结果表明,沈阳市各类水环境样品中总PFCs浓度范围为nd～6.01ng·L-1,平均浓度为5.23ng·L-1.PFOS和PFOA是沈阳地区所有水环境样品中最主要的PFCs污染物,浓度范围分别为nd～2.83ng·L-1和nd～5.71ng·L-1,平均浓度分别为1.11和2.13ng·L-1.细河的PFOS含量最高,约为浑河PFOS含量的2倍,蒲河PFOS含量的3倍.一些PFCs化合物之间呈正相关关系,说明其可能具有相同的来源.PFOS与PFOA之间无相关关系,由此推断沈阳水体中二者具有不同来源.浑河流经沈阳市时,PFOS和PFOA浓度升高.流经沈阳市区后,PFOS和全氟己烷磺酸钾(PFHxS)浓度明显升高.细河中PFHxS也有检出,表明沈阳市是周边水体中PFOS及PFHxS的主要污染来源.丰水期地表水中PFOS和PFOA浓度与枯水期相比没有明显差异,但丰水期水中PFCs组成更为丰富,出现了大量全氟庚酸(PFHpA).沈阳地区自来水中PFOS和PFOA浓度平均值分别为0.39和0.85ng·L-1,最高浓度分别为1.16和2.55ng·L-1,均低于美国饮用水健康参考值.沈阳生物样品中PFOS和全氟十一酸(PFUnDA)是最普遍的化合物.总PFCs平均含量在鱼样品中为6.59ng.g-1(以干重计),鸡和鸭血清样品中分别为1.65和0.69ng·mL-1,鸡和鸭肝脏样品中分别为0.41和1.68ng.g-1(以干重计),与文献报道相比处于较低水平.     

非接触式超声波局放检测仪校验平台研究

非接触式超声波局放检测仪缺乏统一的性能校验平台,影响电力设备局放检测结果的有效性和可靠性,在现有接触式超声波检测平台校验基础上,建立了相应的非接触式超声波局放检测装置校验平台,并提出了模拟装置,实验室环境联合校验方法。所述的校验方法具有稳定性高,重复性好的特点,弥补了非接触式超声波局部放电检测仪在空间,实用性与理想环境差异等问题,有一定的参考价值。     

Characteristics and mixing state of S-rich particles in haze episodes in Beijing

Direct individual analysis using Scanning Electron Microscopy combined with online observation was conducted to examine the S-rich particles in PM_2.5 of two typical polluted haze episodes in summer and winter from 2014 to 2015 in Beijing. Four major types of S-rich particles, including secondary CaSO₄ particles (mainly observed in summer), S-rich mineral particles (SRM), S-rich water droplets (SRW) and (C, O, S)-rich particles (COS) were identified.We found the different typical morphologies and element distributions of S-rich particles and considered that (C, O, S)-rich particles had two major mixing states in different seasons. On the basis of the S-rich particles’ relative abundances, S concentrations and their relationships with PM_2.5 as well as the seasonal comparison, we revealed that the S-participated formation degrees of SRM and SRW would enhance with increasing PM_2.5 concentration. Moreover, C-rich matter and sulfate had seasonally different but significant impacts on the formation of COS.

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Investigation on sampling artifacts of particle associated PAHs using ozone denuder systems

Polycyclic aromatic hydrocarbons （PAHs） are complex organic compounds which are identified as significant carcinogenic to human health. PAHs （mainly in particle phase） are susceptible to atmospheric oxidant gases, especially ozone, nitrogen oxides （NOx）, hydroxyl radical （OH）, and could be degraded on filters during sampling process, leading to an underestimation of ambient PAH concentrations. The goal of this work was to investigate particle associated PAHs sampling artifacts caused by ozone in summer of Beijing. Comparative sampling systems were operated simultaneously during the whole campaign, one with activated carbon ozone denuder, the other being set as conventional sampling system. Activated carbon denuder was testified to be highly efficient to eliminate ozone from air stream. In general, nine particle-bound PAHs observed from conventional sampler were all lower than those from ozone denuder system. The total PAHs （particle phase） concentration was averagely underestimated by 35.9% in conventional sampling procedure. Benzo[a]pyrene （BaP） had the highest percentage of mass loss. founded to have influences Ambient temperature was on PAHs sampling artifacts. High temperature can increase loss of particle associated PAHs during sampling.