基于可调二极管激光技术的汽车尾气遥感监测系统

汽车尾气排放已成为最主要的城市污染源之一。汽车尾气的遥感监测系统作为一种高效实时监测汽车正常运行状况下的尾气排放方法已越来越受到人们的广泛关注。本文主要介绍基于可调二极管激光(TDL)技术的汽车尾气遥感监测系统。首先介绍遥感监测系统的产生与发展以及TDL技术的基本原理,其次阐述遥感监测系统的组成、关键技术以及系统的优点,并分析遥感监测系统在国内外的应用现状,最后提出目前应用中尚待解决的若干关键技术问题。     

响应曲面法优化絮凝处理木薯淀粉废水

采用中心复合实验设计和响应面分析法研究复合絮凝剂聚合氯化铝锌(PAZC)和聚合氯化铝(PAC)混凝处理木薯淀粉废水,进行设计和分析,以溶液pH值和絮凝剂用量为考察因素,分别以COD、浊度去除率为考察指标,选用最佳优化数学模型描述考察指标和考察因素之间的数学关系,并以设定PAZC和PAC对COD去除率(65%),浊度去除率(90%)和SS去除率(90%)的目标值,通过等高线叠加图预测最优实验条件,得到PAZC投量为6.5 mg/L,pH为7.7时,COD去除率和浊度去除率分别达到最大为76.6%和99.9%;PAC投量为19.2 mg/L,pH为7.8时,COD去除率和浊度去除率最大值分别为64.4%和97.1%。经对最优条件进行验证,预测值与验证实验平均值接近。     

Screening 31 endocrine-disrupting pesticides in water and surface sediment samples from Beijing Guanting reservoir

For screening 31 potential or suspected endocrine-disrupting pesticides in water and surface sediments, a multiresidue analysis method based on gas chromatography with electron capture detection (GC/ECD) was developed. Solid phase extraction (SPE) technology with Oasis^® HLB cartridge was also applied in sample extraction. The relevant mean recoveries were 70–103% and 71–103% for water and sediment, respectively. Relative standard deviations (RSD) are 2.0–7.0%, 4.0–8.0% for water and sediment, respectively. Thirty one pesticides (-HCH, β-HCH, γ-HCH, δ-HCH, hexachlorobenzene (HCB), aldrin, heptachlor, endosulfan I & II, p,p′-DDD, o,p′-DDT, p,p′-DDT, p,p′-DDE, endrin aldehyde, endosulfan sulphate, methoxychlor, hepachlor epoxide, -chlordane, γ-chlordane, dieldrin, endrin, dicofol, acetochlor, alachlor, metolachlor, chlorpyriphos, nitrofen, trifluralin, cypermethrin, fenvalerate, deltamethrin) in water and surface sediment samples from Beijing Guanting reservoir were analyzed. Concentrations of pesticides ranged from 7.59 to 36.0 ng g⁻¹ on a dry wt. basis for sediment samples, from 279.3 to 2740 ng l⁻¹ for pore waters and from 48.8 to 890 ng l⁻¹ for water samples, respectively, with a mean concentration of 10.7 ng g⁻¹ in sediment, 735 ng l⁻¹ in pore water and 295 ng l⁻¹ in water, respectively. The data obtained provides information on the levels and sources of endocrine-disrupting pesticides in Guanting reservoir. These results underscore the need to improved environmental protection measures in order to reduce the exposure of the population and aquatic biota to these endocrine-disrupting compounds.     

Kinetics and pathways for the debromination of polybrominated diphenyl ethers by bimetallic and nanoscale zerovalent iron: effects of particle properties and catalyst

Polybrominated diphenyl ethers (PBDEs) are recognized as a new class of widely-distributed and persistent contaminants for which effective treatment and remediation technologies are needed. In this study, two kinds of commercially available nanoscale Fe⁰ slurries (Nanofer N25 and N25S), a freeze-dried laboratory-synthesized Fe⁰ nanoparticle (nZVI), and their palladized forms were used to investigate the effect of particle properties and catalyst on PBDE debromination kinetics and pathways. Nanofers and their palladized forms were found to debrominate PBDEs effectively. The laboratory-synthesized Fe⁰ nanoparticles also debrominated PBDEs, but were slower due to deactivation by the freeze-drying and stabilization processes in the laboratory synthesis. An organic modifier, polyacrylic acid (PAA), bound on N25S slowed PBDE debromination by a factor of three to four compared to N25. The activity of palladized nZVI (nZVI/Pd) was optimized at 0.3 Pd/Fe wt% in our system. N25 could debrominate selected environmentally-abundant PBDEs, including BDE 209, 183, 153, 99, and 47, to end products di-BDEs, mono-BDEs and diphenyl ether (DE) in one week, while nZVI/Pd (0.3 Pd/Fe wt%) mainly resulted in DE as a final product. Step-wise major PBDE debromination pathways by unamended and palladized Fe⁰ are described and compared. Surface precursor complex formation is an important limiting factor for palladized Fe⁰ reduction as demonstrated by PBDE pathways where steric hindrance and rapid sequential debromination of adjacent bromines play an important role.     

Occurrence, sources, and inventory of hexabromocyclododecanes (HBCDs) in soils from Chongming Island, the Yangtze River Delta (YRD)

Hexabromocyclododecanes (HBCDs) is a concern due to their large usage combining with physico-chemical properties and toxicity to wildlife and human. However, very limited data were reported on HBCDs in soils, especially from rural area. In this study, 22 soil samples were collected from Chongming Island at estuary of the Yangtze River Delta, to investigate the level, diasteroisomer profile, potential sources, and mass inventory of HBCDs. The total concentrations ranged from not detected to 93.8 pg g⁻¹ dry weight (dw) with a mean of 23.3 pg g⁻¹ dw, which was at the low end of the global levels. The wide distribution of HBCDs in soils suggested that the local emissions of HBCD-containing materials and/or the inputs via atmospheric transport from other regions were two possible sources. Variation of HBCDs levels was observed in different types of soils. Woodland, tideland and road soils contained slightly higher HBCDs than those of farmland and grassland. Overall, γ-HBCD was the dominant diasteroisomer in soils, followed by α-HBCD and β-HBCD. Significant but weak correlations were only found between α-HBCD and β-HBCD versus TOC content in soils. Currently, the mass inventory of HBCDs in soils of Chongming Island was 5.3 kg. Based on these data, we gave perspective on human intake of HBCDs via soil ingestion by age. Local resident’s intakes ranged from 15.5 to 97.8 fg kg body weight⁻¹ d⁻¹, in which children are exposed more than adults.     

An overview of the methods used in the characterisation of natural organic matter (NOM) in relation to drinking water treatment

Natural organic matter (NOM) is found in all surface, ground and soil waters. During recent decades, reports worldwide show a continuing increase in the color and NOM of the surface water, which has an adverse affect on drinking water purification. For several practical and hygienic reasons, the presence of NOM is undesirable in drinking water. Various technologies have been proposed for NOM removal with varying degrees of success. The properties and amount of NOM, however, can significantly affect the process efficiency. In order to improve and optimise these processes, the characterisation and quantification of NOM at different purification and treatment processes stages is important. It is also important to be able to understand and predict the reactivity of NOM or its fractions in different steps of the treatment. Methods used in the characterisation of NOM include resin adsorption, size exclusion chromatography (SEC), nuclear magnetic resonance (NMR) spectroscopy, and fluorescence spectroscopy. The amount of NOM in water has been predicted with parameters including UV-Vis, total organic carbon (TOC), and specific UV-absorbance (SUVA). Recently, methods by which NOM structures can be more precisely determined have been developed; pyrolysis gas chromatography-mass spectrometry (Py-GC-MS), multidimensional NMR techniques, and Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS). The present review focuses on the methods used for characterisation and quantification of NOM in relation to drinking water treatment.     

活性污泥法的动力学方程讨论及数学模型研究

活性污泥法水处理过程是一个复杂的生化反应过程,伴随有物理化学反应、生化反应、相变过程及物质与能量的转化和传递过程.通过对微生物动力学方程的讨论,进而建立动力学模型,比较了Monod方程和Contois方程分别来模拟有机碳在曝气条件下的生化去除过程.模型主要预测底物浓度、溶解氧、微生物增长等引起的系统响应,为污水处理厂的运行提供指导.     

基于层次分析法的Pedersen人因失误模型研究

科技的发展,使机器设备可靠性有了显著提高,工作环境也得到了改善,但由于人的复杂性,人因失误成为主要的致因因素,如何预防和控制人的失误就成为一个非常重要的课题.运用层次分析法的基本原理,结合Pedersen人因失误模型,构建了导致人因失误的层次分析模型,计算结果显示,人在某种状态下承受负荷的能力大小是影响其失误的主要原因.通过实例,证明了计算结果的可靠性,并提出了减少人因失误的建议.     

典型化工集中区环境空气SVOCs污染特征及来源解析

于冬春两季在华东3个典型石化化工集中区设置环境空气观测点,利用PUF大气被动采样技术(PUF-PAS)采集大气中半挥发性有机化合物(SVOCs),使用气相色谱-质谱联用仪(GC-MS)进行分析.获得59种SVOCs的浓度,包括25种多环芳烃(PAHs)、24种正构烷烃及10种藿烷,并结合主成分分析和特征比值法解析PAHs来源.结果表明:①各观测点正构烷烃贡献率最高,其次是PAHs,分别超过60％和30％;②根据各化合物冬春季浓度变化并结合风向进行分析,推测正构烷烃C18、C29 αβ-藿烷和C30αβ-藿烷与石油化工排放有关;③PAHs单体以菲(Phe)、荧蒽(Fla)、萘(Nap)、芴(Flu)和芘(Pyr)为主,合计占比高达90.0％;④主成分分析显示观测点PAHs主要来自化石燃料燃烧、机动车尾气和石化工艺排放等,3类来源对PAHs的贡献率分别为56.0％、19.2％和8.6％,基于特征比值法的PAHs来源解析予以了验证.     

外源甜菜碱投加增强高盐废水厌氧氨氧化脱氮性能

废水因含盐量高而导致其生物处理效率降低,对于如何提高高盐环境下的生物处理效率已成为目前的研究热点.采用厌氧氨氧化工艺处理高盐废水,以不同甜菜碱浓度对厌氧氨氧化脱氮效能为研究对象,探讨了甜菜碱对厌氧氨氧化脱氮效能的影响.结果表明：①投加甜菜碱对系统脱氮效能有明显的改善作用,甜菜碱浓度为0.1~0.4 mmol·L^-1时,添加甜菜碱缓解了盐胁迫对厌氧氨氧化菌生长的抑制,也促进了反硝化菌的生长;甜菜碱浓度为0.4~0.5 mmol·L^-1时,推测反硝化菌为优势菌群,但对总氮去除表现为促进作用.甜菜碱浓度大于0.5 mmol·L^-1后,添加甜菜碱已无法缓解盐胁迫对反应器脱氮效能的抑制,最终在甜菜碱浓度0.8 mmol·L^-1时对反应器产生完全抑制.②甜菜碱的添加浓度为0.3 mmol·L^-1时,反应去除效能达到最佳,NH₄⁺-N和NO₂^--N分别提升了16%和32%,NRR提升了26.8%.③在最后的恢复试验中,随着甜菜碱浓度的降低反应器脱氮效能得到快速恢复,NH₄⁺-N恢复到50.6%,NO₂^--N平均去除率为63.7%,NRR恢复到0.65 kg·（m³·d）^-1,这说明甜菜碱对反应器的影响是可逆的.