中国显示器件行业VOCs排放特征及控制对策

为掌握和了解我国电子行业VOCs的排放特征,以显示器件行业为研究对象,梳理和分析其生产工艺及排污环节;通过典型企业有机废气的实际排放监测,掌握其VOCs排放水平;利用排放因子法,核算了2011-2016年我国显示器件行业VOCs的排放量,分析其排放量的变化趋势及空间分布特征.结果表明:受产量和污染控制效率变化的双重影响,2011-2016年我国显示器件行业VOCs排放量（文中涉及"全国"的各要素范围均未包含港澳台地区）呈先增后降的趋势,2015年达到最大值（15 605 t）,此后在产量增长放缓和污染控制效率提高的作用下,2016年的排放量有所下降;从排放占比来看,显示器件行业无组织VOCs排放占比从2011年的45%升至2016年的53%,车间无组织VOCs逸散,以及废水处理过程、有机原辅料和有机废液储运等环节的VOCs无组织排放是行业污染控制的重点和难点.研究显示,我国显示器件行业VOCs无组织排放量占比逐年上升,为控制未来行业VOCs排放,企业应将无组织排放转化为有组织排放,之后再通过高效的末端处理装置来减少VOCs排放量.      

Investigating missing sources of glyoxal over China using a regional air quality model (RAMS-CMAQ)

Currently, modeling studies tend to significantly underestimate observed space-based glyoxal(CHOCHO) vertical column densities(VCDs), implying the existence of missing sources of glyoxal. Several recent studies suggest that the emissions of aromatic compounds and molar yields of glyoxal in the chemical mechanisms may both be underestimated, which can affect the simulated glyoxal concentrations. In this study, the influences of these two factors on glyoxal amounts over China were investigated using the RAMS-CMAQ modeling system for January and July 2014. Four sensitivity simulations were performed, and the results were compared to satellite observations. These results demonstrated significant impacts on glyoxal concentrations from these two factors.In case 1, where the emissions of aromatic compounds were increased three-fold,improvements to glyoxal VCDs were seen in high anthropogenic emissions regions. In case 2, where molar yields of glyoxal from isoprene were increased five-fold, the resulted concentrations in July were 3–5-fold higher, achieving closer agreement between the modeled and measured glyoxal VCDs. The combined changes from both cases 1 and 2 were applied in case 3, and the model succeeded in further reducing the underestimations of glyoxal VCDs. However, the results over most of the regions with pronounced anthropogenic emissions were still underestimated. So the molar yields of glyoxal from anthropogenic precursors were considered in case 4. With these additional mole yield changes(a two-fold increase), the improved concentrations agreed better with the measurements in regions of the lower reaches of the Yangtze River and Yellow River in January but not in July.     

生物质锅炉羰基化合物排放特征分析

为了探讨生物质锅炉羰基化合物的排放特征,采用气袋采样-PFPH衍生-GC/MS分析的方法测量了6台生物质锅炉排放烟气中的21种羰基化合物.结果表明,这些生物质锅炉的烟气中羰基化合物排放特征存在明显差异,总体而言,己醛和丙醛浓度在测定的21种目标化合物中比重最高,分别占总量的29%~47%和19%~31%,其次为甲醛和丙酮,乙醛和壬醛.通过羰基化合物排放量与消耗的燃料质量比值估算了排放因子,6台锅炉羰基化合物排放因子介于3.06~18.29mg/kg之间,平均为9.45±6.05mg/kg.采用最大增量反应活性法（MIR）评价了羰基化合物的化学反应活性及臭氧生成潜势（OFP）,平均总的臭氧生成潜势（以O₃计）为5.97gO₃/gVOCs;己醛、丙醛、甲醛对OFP的贡献尤为明显,丙酮虽然占有较高的质量浓度,但对OFP的贡献较低.     

Evaluating the e ects of granular and membrane filtrations on chlorine demand in drinking water

In this study, chlorine decay experiments were conducted for the raw water from Nakdong River that is treated by Chilseo Water Treatment Plant (CWTP) situated in Haman, Korea as well as the e uents from sand and granular activated carbon (GAC) filters of CWTP and fitted using a chlorine decay model. The model estimated the fast and slow reacting nitrogenous as well as organic/inorganic compounds that were present in the water. It was found that the chlorine demand due to fast and slow reacting (FRA and SRA) organic/inorganic substances was not reduced significantly by sand as well as GAC filters. However, the treated e uents from those filters contained FRA and SRA that are less reactive and had small reaction rate constants. For the e uents from microfiltration, ultrafiltration, and nanofiltration the chlorine demand because FRA and SRA were further reduced but the reaction rate constants were larger compared to those of sand and GAC filter e uents. This has implications in the formation of disinfection by products (DBPs). If DBPs are assumed to form due to the interactions between chlorine and SRA, then it is possible that the DBP formation potential in the e uents from membrane filtrations could be higher than that in the e uents from granular media filters.     

Determination of polyfluoroalkyl compounds in water and suspended particulate matter in the river Elbe and North Sea, Germany

The distribution of polyfluoroalkyl compounds (PFCs) in the dissolved and particulate phase and their discharge from the river Elbe into the North Sea were studied. The PFCs quantified included C₄-C₈ perfluorinated sulfonates (PFSAs), 6:2 fluorotelomer sulfonate (6:2 FTS), C₆ and C₈ perfluorinated sulfinates (PFSiAs), C₄-C₁₂ perfluorinated carboxylic acids (PFCAs), perfluoro-3,7-dimethyl-octanoic acid (3,7m₂-PFOA), perfluorooctane sulfonamide (FOSA), and n-ethyl perfluroctane sulfonamidoethanol (EtFOSE). PFCs were mostly distributed in the dissolved phase, where perfluorooctanoic acid (PFOA) dominated with 2.9–12.5 ng/L. In the suspended particulate matter FOSA and perfluorooctane sulfonate (PFOS) showed the highest concentrations (4.0 ng/L and 2.3 ng/L, respectively). The total flux of ΣPFCs from the river Elbe was estimated to be 802 kg/year for the dissolved phase and 152 kg/year for the particulate phase. This indicates that the river Elbe acts as a source of PFCs into the North Sea. However, the concentrations of perfluorobutane sulfonate (PFBS) and perfluorobutanoic acid (PFBA) in the North Sea were higher than that in the river Elbe, thus an alternative source must exist for these compounds.     

Airsolution液体在净化有机废气方面的应用

Airsoluton是一系列植物提取液复配而成的,这些植物提取液是含有气味的有机物,它们是从树、草和花等植物中提取的。这些有味的液体含有大量复杂的化合物,它们是绝大多数植物油的主要成分。本文根据Airsolution液体的氧化性,对处理含苯、甲苯和二甲苯的有机工业废气进行了净化研究,结果表明:Airsolution液体用于处理有机废气是可行的,处理后的苯、甲苯和二甲苯可实现达标排放。且该工艺具有运行费用低,投资少的特点。     

新生产空调客车内挥发性有机物浓度水平和来源分析

选取某厂家新生产的、下线时间不超过28d的53座新空调客车,在车辆处于静止状态下采用二次热解析-毛细管气相色谱/质谱联用法测量新空调车内挥发性有机物的分布特征和浓度水平.根据NIST02标准谱图进行匹配检索,结合色谱保留时间定性,共定性检出33种挥发性有机物,包括烷烃(15种、45.4%)、芳香类化合物(9种、27.3%)、醇(4种、12.1%),酮(3种、9.1%)、酯(2种、6.1%),且大多集中在C6～C10的范围内.新车内浓度最高的前5种挥发性有机物分别为癸烷(8.01 mg/m3)、3-甲基己烷(7.10mg/m3)、庚烷(5.10mg/m3)、异庚烷(4.20 ms/m3)和1-甲基,3-乙基苯(3,56 mg/3),总挥发性有机物TV012,52.5mR/m3.烷烃主要来源于空调车内部保温材料如聚氨酯(PU)发泡海绵或者聚乙烯(PE)发泡材料的释放,而车内检出的芳香族化合物主要来自汽车内饰用胶粘剂、密封胶等的释放.     

室内环境中微生物与挥发性有机化合物相关性的初步探讨

采集室内环境空气中菌落,经培养后分别将微球菌属、葡萄球菌属、芽孢杆菌属、曲霉属、青霉属的纯培养物转接到培养皿上,然后放入环境测试舱密闭环境中进行放大培养。分析菌落放大培养前后环境测试舱内空气中VOCs组成及其含量水平。结果表明,检测的100种挥发性有机化合物中有42种化合物在扩大培养后浓度升高,而30种化合物的浓度下降。微生物在生长代谢过程中既能分解空气中的一些毒害性有机污染物,也能产生一些毒害性有机污染物。     

三维电极法处理苯酚废水影响因素研究

根据电解原理,采用自制三维电极反应器对苯酚废水进行处理。在pH值为3,反应时间为120min,电解电压为15V,极板间距为10cm,曝气强度为0.6m3/h反应条件下,苯酚和COD的最大去除率分别为89.1%和83.2%。表明三维电极法适用于处理浓度较高、且有毒性的废水,是快捷、经济、高效的废水处理方法。     

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.