Spatial distribution of perfluoroalkyl acids in the Pearl River of Southern China

An intensive campaign was conducted in September 2012 to collect surface water samples along the tributaries of the Pearl River in southern China. Thirteen perfluoroalkyl acids (PFAAs), including perfluorocarboxylates (PFCAs, C4–C11) and perfluorosulfonates (PFSAs, C4, C6–C8, and C10), were determined using high-performance liquid chromatography/negative electrospray ionization–tandem mass spectrometry (HPLC/(-)ESI–MS/MS). The concentrations of total PFAAs (ΣPFAAs) ranged from 3.0 to 52 ng L⁻¹, with an average of 19 ± 12 ng L⁻¹. The highest concentrations of ΣPFAAs were detected in the surface water of the Dong Jiang tributary (17–52 ng L⁻¹), followed by the main stream (13–26 ng L⁻¹) and the Sha Wan stream (3.0–4.5 ng L⁻¹). Perfluorooctanoate (PFOA), perfluorobutane sulfonate (PFBS), and perfluorooctane sulfonate (PFOS) were the three most abundant PFAAs and on average accounted for 20%, 24%, and 19% of ΣPFAAs, respectively. PFBS was the most abundant PFAA in the Dong Jiang tributary, and PFOA was the highest PFAA in the samples from the main stream of the Pearl River. A correlation was found between PFBS and PFOA, which suggests that both of these PFAAs originate from common source(s) in the region. Nevertheless, the slope of PFBS/PFOA was different in the different tributaries sampled, which indicates a spatial difference in the source profiles of the PFAAs.     

改良型AO法组合工艺中有机物的三维荧光分析

采用三维荧光(EEM)光谱技术,对上海竹园第二污水处理厂改良型AO法组合工艺运行过程中的各种溶解性有机物(DOM)进行分析,并对比研究传统好氧活性污泥法曝气池出水和A/O脱氮工艺硝化池出水DOM的EEM光谱的迁移变化特性.结果表明,各种DOM中主要的荧光物质有类蛋白质(荧光峰A和B)及类腐殖质(荧光峰C),经改良型AO法组合工艺处理后,荧光峰的强度降低了14％～60％,同时类蛋白质和腐殖质的结构也发生了变化;腐殖酸溯源表明DOM中的腐殖酸以微生物代谢产生的带有荧光基团的腐殖酸类为主.     

两种AHLs信号分子对生物膜法养殖污水处理条件下水体内环境的影响

为提高生物膜法处理养殖污水的效果,对不同信号分子条件下的生物膜处理情况进行研究。在室内循环水养殖系统中,设定3个实验组和1个对照组,分别添加乙醇、C6-HSL、N-3-oxo-C8-HSL和蒸馏水,并在模拟过程中取样分析。实验结果表明,3个实验组附着基上的生物量明显多于对照组,尤其是添加N-3-oxo-C8-HSL组产生的生物量约为对照组的6倍;经添加C6-HSL和N-3-oxo-C8-HSL处理的养殖水体中,亚硝酸盐最终浓度比对照组低28.6%,但无机磷浓度稍高。数据因子分析结果表明,实验过程中(9～27 d),添加AHLs信号因子C6-HSL和N-3-oxo-C8-HSL两组养殖水体内环境的总体得分较高,说明养殖水体的内环境处于较好状态。     

Levels and distribution of Dechlorane Plus in coastal sediments of the Yellow Sea, North China

Dechlorane Plus (DP) has been determined in surface sediments from three Chinese coastal bays, e.g. Jiaozhou, Sishili and Taozi Bay in North China. DP concentrations ranged from <1.2 to 187 pg g⁻¹ dry weight (dw) (mean: 24.7 pg g⁻¹ dw) in Jiaozhou Bay, <1.2 to 135 pg g⁻¹ dw (mean 69.9 pg g⁻¹ dw) in Sishili Bay and <1.2 to 66.7 pg g⁻¹ dw (mean: 40.4 pg g⁻¹ dw) in Taozi Bay, respectively. Additionally, two dechlorinated species were quantified, which accounted for 0.6-5.1% of the ∑DP concentration.The f_syn values (syn-isomer/(syn- + anti-isomer)) in sediments from Jiaozhou Bay (mean 0.29) were close to the technical DP mixture (0.2-0.4), probably indicating local inputs of DP. In contrast, sediments in Sishili and Taozi Bay showed much lower f_syn values (mean 0.16). During transportation the DP isomers are subject to stereo selective degradation which partly resulted in the relative enrichment of anti-DP in coastal sediments.     

树脂吸附-Fenton 试剂氧化法预处理炼油碱渣废水

采用树脂吸附-Fenton 试剂氧化组合工艺对某炼油企业炼油碱渣废水进行预处理.实验确定的最佳工艺条件为:3 种树脂串联吸附,废水流量0.33 mL/ min,H2O2加入量0.20 mol / L,n（H2O2）1 n（Fe2 +）= 12,Fenton 试剂氧化进水pH 3,Fenton 试剂氧化反应时间120 m...     

磁性生物膜载体的规模化制备、表征和应用

利用机械力化学表面改性原理设计了卧式双旋搅拌混合反应设备,通过磁铁矿粉和适量浓硫酸的球磨混合反应制备得到磁性生物膜载体,其XRD、IR、SEM和BET表征分析结果表明,磁性生物膜载体表层生成了多羟基硫酸铁为主的活性组分.进而在膜生物反应器实验装置中投加磁性生物膜载体进行了中试实验,结果表明,磁性生物膜载体能与活性污泥中的微生物聚合形成稳定的菌胶团,活性污泥SV30从实验初期89％降到了稳定期的39％,此外,磁性生物膜载体还具有稳定膜生物反应池出水COD,强化脱氮除磷的能力.     

基于高性能GPU计算的城市建筑群震害模拟

为适应不断提高的震害预测需求,精细化模型已经成为城市区域震害预测的主要发展方向。然而传统的基于CPU平台的计算方法成本过高,使得精细化模型的应用受限。近年来,GPU技术由于其强大的并行计算能力和较为低廉的价格优势,在通用计算领域得到了快速的发展和应用。基于GPU-CPU协同计算技术,建立了城市区域震害的计算模拟方法,显著缩短了城市区域震害预测的时间。并采用该方法对某中型城市的真实震害进行了模拟应用,展示了GPU技术在大区域城市建筑群震害模拟中的独特优势。     

火电燃料消费过程对资源环境的影响评估

我国以化石能源为主要燃料的火电生产导致了严重的资源枯竭和环境污染问题,定量评估火电燃料消费对资源环境的影响是区域可持续发展研究的重要内容。在估算火电燃料燃烧及运输、生产过程中排放的主要大气污染物的基础上,利用成分法计算相应的生态足迹,定量评估火电燃料消费过程对资源环境的影响。结果表明：我国1 kW〖DK〗·h火电的燃料消费过程中排放的CO2、CH4、NOx、SO2、烟尘分别为107 kg、993×10-3 kg、646×10-3 kg、260×10-3 kg、202×10-2 kg;全国火电燃料消费占用的生态足迹由2000年的50 67444万hm2,增加到2007年的123 84208万hm2,年均增长1362％;CO2和NOx的生态足迹平均比重高达836％,是影响资源环境的主要因子,SO2、烟尘与CH4三者合计仅164%,对资源环境的冲击相对较小     

中国人口集疏格局与形成机制研究

人口集聚和疏散是人口空间分布格局最直观和最集中的体现,基于人口集聚度的中国人口集疏的空间格局和形成机制的研究,有助于准确把握中国人口空间分布的基本脉络,具有重要的学术价值和实践意义。研究采用了人口集聚度分级评价的方法,依据人口集聚度的不同,将各个地区划分为不同等级的人口集聚区,并对其分别讨论。在此基础上,结合中国人口分布格局、自然条件的空间分布格局、人居环境自然适宜性评价结果以及经济发展格局和城市化格局,对中国的人口集疏的空间格局进行了归纳,并进一步对相应的形成机制进行了探讨,得出了我国人口分布的空间不平衡日益加剧,并呈现沿海、沿江、沿线集聚的态势的基本结论,并对我国人口分布集疏格局的形成进行了探讨,提出了自然因素奠定我国人口分布的基本格局,而经济发展不平衡与城市化成为人口集聚的动力的观点。     

Impact of carbon source on nitrous oxide emission from anoxic/oxic biological nitrogen removal process and identification of its emission sources

Wastewater treatment is an important source of nitrous oxide (N₂O), which is a strong greenhouse gas and dominate ozone-depleting substance. The purpose of this study was to evaluate the effect of carbon source on N₂O emission from anoxic/oxic biological nitrogen removal process. The mechanisms of N₂O emission were also studied. Long-term experiments were operated to evaluate the effect of three different carbon sources (i.e., glucose, sodium acetate, and soluble starch) on N₂O emission characteristics. And batch experiments, in the presence or absence of specific inhibitors, were carried out to identify the sources of N₂O emission. The ammonia-oxidizing bacteria (AOB) and denitrifiers community compositions under different circumstances were also analyzed based on which the underlying mechanisms of N₂O emission were elucidated. The conversion ratios of N₂O in reactors with glucose, sodium acetate, and soluble starch were 5.3 %, 8.8 %, and 2.8 %, respectively. The primary process responsible for N₂O emission was nitrifier denitrification by Nitrosomonas-like AOB, while denitrification by heterotrophic denitrifiers acted as the sink. Reactor with sodium acetate showed the highest N₂O emission, together with the highest nitrogen and phosphate removal ratios. Carbon source has a significant impact on N₂O emission quantity and relatively minor effect on its production mechanism.