γ-射线辐照法改善城市污水厂剩余污泥厌氧消化特性的研究

采用γ-射线辐照法对城市污水厂剩余污泥进行预处理，从固体组分、可溶性组分及厌氧产气量等角度来探讨γ-射线辐照法改善城市污水厂剩余污泥厌氧消化特性的可行性。结果表明，经γ-射线辐照处理后，污泥的平均粒径减小，在辐照剂量为6．51-30．75kGy范围内，粒径的减小率达30％-50％；可溶性有机组分随着辐照剂量升高而增加，当辐照剂量为19．4kGy时，SCOD增加率达552．5％；与未辐照相比，污泥经2．48、6．51、11．24kGy辐照处理后，厌氧消化累计产气量分别增加8．89％、19．74％和35．81％。γ-射线辐照法是一种有效的改善污泥厌氧消化特性的方法，11．24kGy左右的剂量可作为污泥预处理的最佳剂量。     

铁炭法处理高浓度难降解表面活性剂废水的研究

就铁炭法对高浓度难降解拉开粉（阴离子表面活性剂）废水的处理效果进行了接近工业化的动态模型实验研究，结果表明酸化铁炭工艺对橡胶工业拉开粉废水具有显著的去除效果。在Fe：C=2：1，pH=4，停留时间60min，曝气量0．1m^3／h时，拉开粉（BX）和COD的总去除率分别约为80％和45％。     

Using a process-based model to understand dynamics of Chinese agricultural and water technology development from 8000 bc to 1911 ad

Advancements in technology are inextricably bound to our society and the natural environment. However, how the development process of a technology system interacts with both remains unclear. We propose a process model to understand the complex dynamics among technology, society, and the environment via seven interactive elements: technologies, actors, receiving bodies, natural contexts, social contexts, temporal–spatial contexts, and outcomes. The model was applied to agricultural and water technology development in China from 8000 bc to 1911 ad. Our findings show that these elements did not play equally important roles in different periods of the development in ancient China, with social contexts most dominating during the earlier periods and both social and environmental concerns arising towards the later periods. The proposed model, by identifying the elements in the technology development that should be strengthened, can act as an analysis device to assist in reconfiguring a more sustainable socio-technological system.Electronic supplementary materialThe online version of this article (10.1007/s13280-020-01424-7) contains supplementary material, which is available to authorized users.     

城市污水处理厂除臭技术

介绍了城市污水处理厂臭气来源、成分及产量。针对目前国内外除臭技术的研究和发展情况，分析了污水处理厂的各种物理、化学和生物除臭方法的技术原理、优缺点和应用现状。结合日本城市污水处理厂的运行实际，重点介绍了一种不产生臭气的新技术——腐殖活性污泥法的工艺流程、特点及其应用现状。     

Photocatalytic reactions of phenanthrene at TiO2/water interfaces

The photocatalytic oxidation of phenanthrene was investigated in aqueous TiO2 suspensions under UV light irradiation. Chemical oxygen demand (COD) measurements, UV-Vis spectrophotometer, IR spectrometer and gas chromatography-mass spectrometry (GC-MS) analytical techniques were used to monitor the reaction process. Some factors affecting the photodegradation rate were studied and some aromatic intermediates were detected during the reaction process. Fast and complete mineralization of phenanthrene was achieved in this reaction system.     

超声波强化污水厌氧生物处理综述

通过对超声波辐射促进微生物活性以及超声波强化污水好氧生物处理、厌氧污泥减量化处理等作用机制的分析研究,探讨将超声波应用于强化污水厌氧生物处理的可行性.同时对超声波强化污水厌氧生物处理的应用前景进行了展望.     

Generator column determination of aqueous solubilities for non-ortho and mono-ortho substituted polychlorinated biphenyls

Aqueous solubilities of four non-ortho and eight mono-ortho substituted PCBs were determined using a generator-column technique followed by subsequent off-line GC/ECD analysis of the aqueous solutions. The method is based on pumping water through a column containing glass beads coated with the congener being studied and has been used to measure solubilities at room temperature. The method circumvents many of the experimental difficulties encountered with the traditional shake-flask system. Aqueous solubility of 3,3′,4,4′-tetrachlorobiphenyl determined by this procedure is compared with data obtained from the shake-flask method and the computational method. The precision of replicate measurements is better than ±6.5%. Aqueous solubilities determined for 12 congeners ranged from 6.07 × 10⁻¹¹ to 4.47 × ⁻⁹ mol/L and generally decreased with molecular weight and increased with degree of ortho-chlorine substitution within a molecular-weight class.     

白洋淀几种不同食性鱼类对六六六、DDT的富集

对白洋淀几种不同食性鱼体内六六六和ＤＤＴ残留量分析表明，草食性鱼体内农药残留量最少，六六六含量为５９．３μｇ／ｋｇ，ＤＤＴ含量为２９．６μｇ／ｋｇ；其次是杂食性鱼类，六六六含量为９０．４μｇ／ｋｇ，ＤＤＴ含量为１０８．５μｇ／ｋｇ；肉食性鱼体内农药残留量最高，六六六含量为１１０．７μｇ／ｋｇ，ＤＤＴ含量为１２４．４μｇ／ｋｇ。鱼体对ＤＤＴ的浓缩因子为３１１～１２４４，明显高于六六六的１７７～３６８。鱼体内ＢＨＣ４种异构体的残留顺序为δ＞α＞γ＞β，与其在水体中的比例α＞γ＞δ＞β略有不同。鱼体内ＤＤＴ主要以代谢物ｐ，ｐ＇－ＤＤＥ的形式存在，但个别样品中少量的ｐ，ｐ＇－ＤＤＤ及ｏ，ｐ＇－ＤＤＴ的检出，表明白洋淀水生生态系统最近受到ＤＤＴ的轻度污染。本项研果与１９７５～１９７７年检测结果进行比较；白洋淀鱼体内六六六残留量显著下降，下降率为１５．８％～７９．２％；ＤＤＴ残留量却明显增加（草食性鱼类除外），增加率约为４７．８％～９７．８％。     

TiO2 photocatalytic degradation of PCBs in soil-water systems containing fluoro surfactant

Titanium dioxide-mediated photodegradation of Polychlorinated biphenyls (PCBs) in soil/aqueous systems with added fluorinated surfactant was investigated. PCBs can bind tightly to organic matter in the soil, especially in aged, contaminated soil. Experiments showed an effective PCB photocatalytic degradation in mixed systems of soil/clay with anionic fluorinated surfactant FC-143 and TiO2. The FC-143 surfactant is stable in this photochemical process. PCB degradation rates in samples followed the order: spiked clay > spiked soil > Hudson River bank soil. The results suggest that anionic fluorinated surfactant may form semimicelles and/or admicelles on the surface of positively charged TiO2. The hydrophobic surface of TiO2 can provide a nonpolar phase that acts as a partioning medium for hydrophobic PCBs. Therefore, PCBs in soil can be released to the semimicelle and/or admicelle on the TiO2 surface and are effectively photodegraded in a dispersion containing anionic fluorinated surfactant. The combination of surfactant extraction and photooxidation forms the basis for a novel two-stage process for the removal and destruction of PCBs from soil.     

Photooxidation mechanism of nitrogen-containing compounds at TiO2/H2O interfaces: an experimental and theoretical examination of hydrazine derivatives

The photocatalytic oxidation of oxalyldihydrazide, N,N'-bis(hydrazocarbonyl)hydrazide, N,N'-bis(ethoxycarbonyl)hydrazide, malonyldihydrazide, N-malonyl-bis[(N'-ethoxycarbonyl)hydrazide] was examined in aqueous TiO2 dispersions under UV illumination. The photomineralization of nitrogen and carbon atoms in the substrates into N2 gas, NH4+ (and/or NO3-) ions, and CO2 gas was determined by HPLC and GC analysis. The formation of carboxylic acid intermediates also occurred in the photooxidation process. The photocatalytic mechanism is discussed on the basis of the experimental results, and with molecular orbital (MO) simulation of frontier electron density and point charge. Substrate carbonyl groups readily adsorb on the TiO2 surface, and the bonds between carbonyl group carbon atoms and adjacent hydrazo group nitrogen atoms are cleaved predominantly in the initial photooxidation process. The hydrazo groups were photoconverted mainly into N2 gas (in mineralization yields above 70%) and partially to NH4 ions (below 10%). The formation of NO3- ions was scarcely recognized.