生物膜微环境和传质现象研究进展

生物膜法污水处理工艺对污染物的降解去除主要依赖活性生物膜,研究生物膜的结构和传质特性是揭示反应机理和提高反应器处理效率的重要手段.综述了近年来国外在生物膜微环境和微观传质过程中的研究进展,包括对生物膜微观结构的解析、膜内不同菌系的分布特征及其功能以及生物膜的传质现象和数学模型.在此基础上,提出了生物膜研究领域今后应开展的研究方向.     

THE EFFECT OF ICE COVER ON VERTICAL TRANSFER IN STREAM CHANNELS1

ABSTRACT: The effect of ice cover on vertical transfer is examined based on the Reynolds' analogy and composite logarithmic velocity distributions. A finite difference scheme is used to predict concentration profiles in a two-dimensional channel. Comparisons made between the ice-covered condition and the ice-free condition show that considerable reduction in mixing capacity of the channel is caused by the ice cover.     

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.     

基于车载诊断系统的轻型乘用车实际道路油耗特征分析

近年来的一系列研究表明,轻型车实际道路油耗与型式认证油耗间的差异在不断增大,之前的实际道路油耗研究大多基于用户上报数据或车载排放测试系统(PEMS).车载诊断系统(OBD)是一种监测发动机及排放控制系统实时工作状态的仪器.本研究通过OBD解码器采集瞬时发动机进气量计算机动车瞬态油耗并通过2辆轻型汽油车的实验室台架测试证明该方法具有很好的准确性(差异在±5%以内).本研究进一步在北京选取了7辆轻型汽油车,利用OBD解码器开展实际道路油耗测试,并研究运行工况及车辆载重对其实际道路油耗的影响.实际道路结果显示测试车辆在典型工况下的油耗比型式认证油耗高23.1%~46.4%,平均差异为29.2%.通过微观运行模态方法将实际道路油耗修正到法规测试循环(NEDC工况)的交通特征下,道路油耗仍然比型式认证油耗高18.7%±7.1%.研究表明,平均速度与实际道路油耗具有很强的相关性.实际道路油耗在30 km·h-1以下时会随速度降低而显著上升.此外,研究还发现如果车辆载重增加260 kg,实际道路油耗将上升6.2%±2.2%.     

基于动态质量平衡的室内颗粒物沉降规律研究

目前室内颗粒物污染问题已经受到广泛关注.越来越多的流行病学研究表明,大气悬浮颗粒物浓度对人体健康存在显著的负影响.由于个人在室内滞留的时间可能超过全天时间的90％,因此剖析室外颗粒物向室内的传输渗透机理,对掌握室内微环境下的颗粒浓度水平至关重要.本实验以青岛一办公室为研究对象,使用具有4个尺寸间隔的光学计数器同时测量室内和室外的颗粒物浓度,粒径分布范围在0.3~2.5μm,采集时间为2016年4月~9月.根据实验数据,采用基于时间的动态质量平衡模型,估算了换气次数在0.03~0.25h^-1范围内的室内颗粒物渗透率和沉降速率分别为0.45~0.82h^-1和0.94~2.82m/h,并分析了这些参数随粒径大小的变化规律.其结论为进一步研究颗粒物在室内的传输机理和运动轨迹提供参数.     

南极拉森北部冰架表面物质损失机制探讨

基于解密航片、光学遥感影像以及卫星雷达测高数据,完成一个较长时间序列的拉森A和B冰架的范围及表面高程变化监测.在此基础上,结合NCEP/NCAR夏季逐月平均气温数据和GPCP全球降水数据这两种气象数据来探讨拉森北部冰架表面物质平衡机制.结果表明：随着气温的升高,拉森A和B冰架自1968年以来总共消失了14 000km²的浮冰.当前,拉森A冰架已经完全消失,拉森B冰架仅存2 000km².伴随着冰架的持续崩塌与退缩,拉森北部冰架展现出高程持续降低的趋势,而且拉森A冰架的降低速度（-0.45m/a）明显高于拉森B冰架（-0.09m/a）.作为冰架表面物质平衡估算的两个主要参数,拉森A冰架的夏季平均气温从1968年的0.16℃升高到近期的0.84℃;拉森B冰架的夏季平均气温从1968年的0.04℃升高到近期的0.66℃.过去几十年的降水量变化对拉森北部冰架表面物质累积产生的影响很小,反倒是夏季温暖的降雨进一步加剧该地区的表面物质负平衡.对于持续崩塌与退缩型的拉森北部冰架来说,其高程降低除了受到冰架表面冰雪融化与再凝结导致的积雪致密化驱动外,还受到冰架后退导致的背向应力减少,进而导致的冰架物质输送加快的深刻影响.总之,在全球气候变暖的背景下,拉森A和B冰架的表面物质体现出越来越明显的负平衡趋势.     

Measurement of hydrogen peroxide and organic hydroperoxide concentrations during autumn in Beijing, China

Gaseous peroxides play important roles in atmospheric chemistry. To understand the pathways of the formation and removal of peroxides, atmospheric peroxide concentrations and their controlling factors were measured from 7:00 to 20:00 in September, October, and November 2013 at a heavily trafficked residential site in Beijing, China, with average concentrations of hydrogen peroxide (H₂O₂) and methyl hydroperoxide (MHP) at 0.55 ppb and 0.063 ppb, respectively. H₂O₂ concentrations were higher in the afternoon and lower in the morning and evening, while MHP concentrations did not exhibit a regular diurnal pattern. Both H₂O₂ and MHP concentrations increased at dusk in most cases. Both peroxides displayed monthly variations with higher concentrations in September. These results suggested that photochemical activity was the main controlling factor on variations of H₂O₂ concentrations during the measurement period. Increasing concentrations of volatile organic compounds emitted by motor vehicles were important contributors to H₂O₂ and MHP enrichment. High levels of H₂O₂ and MHP concentrations which occurred during the measurement period probably resulted from the transport of a polluted air mass with high water vapor content passing over the Bohai Bay, China.     

Removal of hydrophobic volatile organic compounds with sodium hypochlorite and surfactant in a co-current rotating packed bed

A co-current flow rotating packed bed was applied to remove volatile organic compounds(VOCs) by sodium hypochlorite(Na Cl O) and surfactant(sodium dodecyl benzene sulfonate,SDBS) from air stream. Xylene was used as a model VOC herein. The effect of p H,concentration of Na Cl O and SDBS solution, liquid flow rate, gas flow rate and rotational speed on xylene removal efficiency and overall mass transfer coefficient(KGa) were discussed. Then, a correlation for KGa of the co-current rotating packed bed was proposed by fitting the experimental data of KGa and independent variables of liquid/gas ratio,rotational speed, p H, Na Cl O concentration and treatment time, which was in good agreement with the experimental data(the deviation ≤± 30%).     

京津冀中部夏季大气颗粒物空间分布特征

为研究京津冀地区雾霾成因,以Y-12（运-12）飞机为大气颗粒物观测平台,对2016年夏季京津冀中部大气颗粒物污染特征进行了观测研究.结果表明,天津市颗粒物数浓度垂直分布特征为1 500 m（以下均为标准气压高度）以下呈单峰分布,1 500 m以上呈单调下降,峰值均出现在0.35~0.40 μm之间,峰值的最大值出现在900 m左右;颗粒物体积浓度谱呈三峰分布,分别在0.30~0.40、0.50~0.60和1.00~2.00 μm之间,峰值的最大值出现在450 m左右.天津市、保定市和衡水市600与2 400 m数浓度谱分布特征为单调下降和单峰分布并存;600 m表面积浓度谱呈三峰分布,分别在0.30~0.40、0.50~0.60和0.90~1.00 μm之间;2 400 m表面积浓度谱呈双峰分布,分别在0.30~0.40和0.50~0.60 μm之间;600与2 400 m体积浓度谱均呈三峰分布,分别在0.30~0.40、0.50~0.60和1.00~3.00 μm之间.天津市大气颗粒物数浓度谱峰值的最大值出现在900 m左右,说明逆温层对气溶胶累积的形成有重要影响.城市间数浓度谱峰值高低受地面颗粒物质量浓度大小影响.京津冀中部大气颗粒物表面积浓度谱在600 m呈三峰分布,在2 400 m呈双峰分布,可能是因为2 400 m空中以细粒子为主.京津冀中部大气颗粒物体积浓度谱在600与2 400 m空中均为三峰分布,而国外为双峰分布,发现粗粒子峰值粒径范围差别较大,这是由于国内PM_2.5在PM₁₀中占比较大.研究显示,京津冀中部600和1 200 m大气颗粒物多来源于山东、河南,经近地面输送;2 400 m大气颗粒物多来源于内蒙古地区,经高空和近地面两种途径输送.      

郑州市PM2.5化学组分的季节变化特征及来源解析

为了解析郑州市PM_2.5的污染特征和来源,同时为了研究不同季节以及市区和市郊之间的差异,本研究于2018年四季在郑州市环境保护监测中心站（市区）和郑州大学（市郊）点位共计采集环境PM_2.5有效样品1284个.通过离子色谱仪、碳分析仪和X射线荧光光谱仪分别测试得到9种无机水溶性离子、两种碳组分和27种元素浓度,分析了郑州市城郊PM_2.5中化学组分的季节变化特征,使用富集因子法、地累积指数法、化学质量平衡模型、后向轨迹法和潜在源贡献因子法,研究了郑州市城郊不同季节PM_2.5的来源差异.结果表明,市区和市郊点位年平均PM_2.5浓度达到（59.7±24.0）μg ·m^-3和（74.7±13.5）μg ·m^-3,郊区点位（除冬季外）季节平均浓度均高于市区点位,季节均值呈现冬季 > 秋季 > 春季 > 夏季的变化.市郊春季受地壳物质的影响较大,夏秋两季全部组分浓度均高于市区;冬季市区受燃煤源和机动车源影响更大.Cu、As、Zn、Pb和Sb受到人为源的影响强烈,市区富集程度更大,Zn、Cu、As和Pb存在一定的潜在生态风险.源解析结果显示,两点位春夏秋冬四季均分别受到扬尘源、二次硫酸盐、二次硝酸盐和燃煤源的较大影响,此外,市区四季受二次污染源和机动车源的影响较大,而市郊秋冬季受生物质源影响较大.来自山东的气团、西北方向的气团（除夏季外）、南方气团（除冬季外）对郑州市PM_2.5的污染水平影响较大,其潜在来源区域主要为省内及与邻省的交界处.