WHO-IRC和IAEA-AQCS国际比对样品的γ谱分析

报道了本实验室１９９１－１９９４年间参加ＷＨＯ－ＩＲＣ和ＩＡＥＡ－ＡＱＣＳ组织的环境样品放射性测量国际化对工作。用２台ＨＰＧｅγ谱仪,相对方法和效率曲线方法测量了土壤样品,用自吸收校正方法测量了生物样品。对ＷＨＯ－ＩＲＣ Ｎｏ．５７Ｖｉ３００号样品,在２８个报出实验室中,本实验室测量值与推荐值的平均相对偏差最小,为３．０４％。     

厌氧氨氧化启动过程细菌群落多样性及PICRUSt2功能预测分析

细菌群落是实现厌氧氨氧化系统高效脱氮的核心,而厌氧氨氧化启动过程细菌群落多样性及其功能特征仍未被充分阐明.本研究采用升流式厌氧污泥床（UASB）反应器进行厌氧氨氧化系统启动,利用16S rRNA基因高通量测序技术并结合PICRUSt2功能预测分析,研究启动过程不同时间（d0、d30、d60和d90）细菌群落多样性及功能动态变化特征.结果表明,启动过程共检测到48个门、111个纲、269个目、457个科、840个属和1497个种;Candidatus_Brocadia和Candidatus_Kuenenia为检测到的厌氧氨氧化菌,且它们的相对丰度在启动过程不同时间存在显著差异（P<0.05）.启动过程,细菌群落α多样性指数整体呈现显著的降低趋势（P<0.05）,细菌群落结构呈现出明显的空间分异特征,且差异显著（R=0.846,P<0.01）.PICRUSt2功能预测分析表明,启动过程,细菌群落具有丰富的功能多样性,一级功能层表现为有机系统和代谢方面较为活跃,二级功能层子功能基因丰度在厌氧氨氧化启动过程发生明显变化;细菌群落涉及49个参与氮素代谢的相关功能基因,且不同时间阶段参与硝化、反硝化、厌氧氨氧化、硝酸盐同化/异化还原和亚硝酸盐同化/异化还原过程的相关功能基因丰度发生明显变化.     

海底铁锰氧化还原过程的模拟研究

本文用室内海水-沉积物平衡箱研究了沉积物间隙水中铁、锰的垂直变化分布和随时间变化的分布,Fe~(2+)随深度、时间的变化幅度大,在六个月的实验期内均是如此,而Mn~(2+)在放置三个月后即趋于稳定;Fe~(2+),Mn~(2+)产生的宏观经验动力学表明:Fe~(2+)受pH影响远比Mn~(2+)大,且随着深度的增加更为明显,Fe~(2+)在较下层产生速率大,而Mn~(2+)反之;Fe~(2+)的扩散转移是上覆海水向沉积物中转移,扩散量为-60.7ug/m~2d,Nn~(2+)转移方向相反,扩散量为1746.2ug/m~2.d。     

聚硅硫酸铁（PFSS）的混凝性能及其应用

本文研究了聚硅硫酸铁的混凝性能和稳定性，试验了它对煤矿洗煤水，矿井水，以及城市废水的混凝处理效果，结果发现，随Ｆｅ／Ｓｉ摩尔比的增大，聚硅硫酸铁的混凝效果明显提高；与聚硅酸相比，聚硅硫酸具有较好的稳定性和较强的除浊脱色性能。     

直接驯化嗜盐菌处理高盐废水的研究

从大连旅顺盐场底泥中筛选出适合高盐度的嗜盐菌,在序批式间歇反应器(SBR)中对其进行3.5%(质量分数)盐度的驯化,污泥混合液悬浮固体(MLSS)平均质量浓度达600mg/L。污泥比耗氧速率(SOUR)测量结果显示,内源呼吸阶段污泥SOUR为10.36mg/(g.h),外源呼吸阶段污泥SOUR达到29.09mg/(g.h),表明所筛选的嗜盐菌培养的污泥具有较高活性。利用培养的污泥进行高盐模拟废水处理试验,结果表明,对盐度为3.5%、COD为240～340mg/L的高盐废水,在每周期12h、曝气量0.6L/min、污泥MLSS为600mg/L、污泥龄为18d条件下,COD去除率达95%以上,NH4+-N去除率达61%,TP去除率达55%。改变进水有机负荷对出水COD去除影响不大,该系统耐有机负荷冲击能力较强;盐度负荷的改变对COD的去除影响不大,而NH4+-N去除率有明显变化,在3.5%和5.0%的盐度下,NH4+-N去除率分别为61%和31%。     

Effects of solution conditions on the precipitation of phosphate for recovery. A thermodynamic evaluation

To understand the effects of solution conditions on the precipitation of calcium phosphates from wastewater for recovery, a computer programme PHREEQC was employed to calculate the speciation and saturation-index (SI) with respect to hydroxyapatite of a chemically defined precipitation system, which contains phosphate of 1–200 mg P/l, with Ca/P molar ratios of one to 10 times of the stoichiometric calcium to phosphorus molar ratio of hydroxyapatite, at a pH range of 7.0–11.0. The results show that the SI is respectively the logarithmic function of the phosphate concentration and the calcium concentration, increasing with the increase of either of them; the SI is a polynomial function of the solution pH value and increases with its increase, and the effect of solution pH value is due to its influence on base uptake of the precipitation reaction and the speciation of phosphate and calcium ions; the SI is also a logarithmic function of the solution ionic strength but decreases with its increase; at the temperature range of 5–30 °C the SI increases linearly with solution temperature and the effect of temperature is also due to its influence on the speciation of phosphate and calcium ions.     

一体化间歇曝气完全混合活性污泥法

一体化间歇曝气完全混合活性污泥法处理装置采取特殊的沉淀区构造,改变了活性污泥的循环流动方式,通过间歇曝气,反应区交替处于好氧/缺氧状态,达到了有机物高效去除、高效硝化反硝化及控制污泥膨胀的效果.该方法具有出水水质好、运行稳定、能耗低、流程简洁和操作管理方便的特点,是一种很有发展潜力的一体化中小型生活污水、城市污水处理系统.     

Comparative study of extraction methods for the determination of PAHs from contaminated soils and sediments

The following four methods were compared on the extraction efficiency of 16 EPA (US Environmental Protection Agency) polycyclic aromatic hydrocarbons (PAHs): German method of the Verband Deutscher Landwirtschaftlicher Untersuchungs und Forschungsanstalten (VDLUFA), two methods of the International Organization for Standardization using shaking (ISO A) and Soxhlet extraction (ISO B) and an ultrasonic method. Recovery rates of 16 PAHs were determined in two soils. Extraction efficiency was evaluated in five soils and three sediments. Effect of drying soils and sediments on extraction efficiency was tested using the VDLUFA and the ultrasonic methods. Our study shows that the number of aromatic rings, rather than extraction procedures, significantly influenced recovery rates of individual PAHs. No significant differences in extraction efficiency of the four methods were observed for less polluted samples. For highly polluted soils, extraction efficiency decreased in the following order: VDLUFA method > ISO A > ultrasonic method > ISO B. Influence of soil moisture on extraction efficiency depended to some extent on both solvent used and content of PAHs in samples. A mixture of dichloromethane/acetone (5:1) is recommended for PAH extraction from moist samples when the ultrasonic method is used.     

Distribution of polycyclic aromatic hydrocarbons in agricultural soils in South Korea

The content and type of polycyclic aromatic hydrocarbons (PAH) in soils from paddy fields and upland areas in South Korea were determined using gas chromatography linked to mass spectrometry (GC–MS). The distribution map of total PAH content was obtained as a contour plot using a geographical information system. The overall distribution of PAH was found to be closely related to the pollution sources, the size of city and the type of industry. The average content of total PAH in all samples was 236 μg kg⁻¹, and the range was from 23.3 to 2834 μg kg⁻¹. The highest concentrations were found in soils sampled near iron processing plants. The concentration of PAH decreased in the order fluoroanthene>benzo(b)fluoroanthene>pyrene. Special PAH compound ratios, such as phenanthrene/anthracene and fluoroanthene/pyrene, were calculated to evaluate the origin. The collected data suggested that the pyrogenic origins such as motor vehicle exhaust and heavy industry emission were the dominant source of PAH in Korean soils.     

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.