ABR反应器预处理综合印染废水研究

采用ABR反应器预处理难降解印染废水中试研究。结果表明，ABR反应器最佳水力停留时间（HRT）为24 h，ABR反应器稳定运行4个月，当进水COD平均值为769.4 mg/L（最高1 060 mg/L，最低590.6 mg/L），色度平均值为351倍时，出水COD和色度分别为424.2 mg/L和83倍，去除率分别为44.5%和76.1%。印染废水B/C由0.27提高到0.42，废水可生化性明显改善。     

水力停留时间对厌氧折流式反应器处理印染废水运行效果影响的研究

采用厌氧折流式反应器(ABR)处理印染废水。结果表明,在水力停留时间(HRT)为14～32h时,ABR各格室出水COD逐渐降低,HRT越长,COD去除率越高;进水色度为300～500倍,ABR对色度去除效果显著,在HRT为32h时,色度去除率高达75.0%;ABR各格室出水NH3-N均比进水高,第1格室的NH3-N较进水增幅最大;ABR各格室pH呈上升趋势;氧化还原电位(ORP)随ABR格室依次下降;在HRT为14～32h时,BOD5/COD由进水的0.23分别提高到出水的0.31、0.36、0.42、0.40。从运行管理的经济性和提高出水的可生化性考虑,处理印染废水的HRT选择24h为佳。     

厌氧折流板反应器处理生活污水的运行特性

以厌氧消化污泥作为厌氧折流板反应器ABR的接种污泥,研究恒温(35℃)条件下ABR处理生活污水的启动和运行特性。实验结果表明,ABR反应器仅用了39 d就完成初次启动,COD去除率一直稳定在60%左右。在以后运行的5个阶段里,即当水力停留时间为4~10 h,容积负荷为1.17~2.9 kg COD/m3.d,反应器对COD的平均去除率基本稳定在70.49%~80.2%;并且当HRT=7 h,VRL=1.612 kg COD/m3.d时,反应器对COD的去除率平均高达80.2%,平均COD出水低于100 mg/L。在实验过程中(除启动阶段外),反应器出水碱度均远远大于进水碱度,VFA均在1.5 mmol/L以下。     

A/O+MBR工艺处理玉米深加工废水的中试研究

实验基于企业污水站的改造工程,研究了MBR对玉米深加工废水的处理效果并对工艺运行参数优化提出建议.结果表明,该工艺对COD的去除率可以达到90％以上,出水稳定在26 mg/L左右;出水NH4-N达到1 mg/L以下;TN去除率达到70％以上,出水TN达到10 mg/L以下,出水完全达到排放标准.通过4种工况的比较,说明在污泥浓度8 g/L左右,曝气池内DO在3 mg/L左右,MBR内DO＞4 mg/L,好氧段停留时间13.5 h,并保证3h以上的缺氧段水力停留段时间的条件下,A/O+ MBR工艺可以有效去除玉米深加工废水中的污染物.     

ABR-好氧颗粒污泥处理黄连素废水的启动研究

实验研究了ABR-好氧颗粒污泥组合工艺处理黄连素制药废水的启动运行,通过分析发现,ABR装置在HRT为4 d,黄连素浓度为50 mg/L的运行方式下成功启动,反应器运行稳定后每个格室MLSS平均值分别为25 840、21 560、27 500和11 200 mg/L。以ABR出水为营养物,成功培养出粒径在2～10 mm,沉降速率为104～137 m/h,沉降性能优良的好氧颗粒污泥。该组合工艺在启动实验的末期,进水COD浓度为3 000～4 000 mg/L左右,出水COD浓度到达168.4～271mg/L,系统总的去除率保持在90%～95%之间,表明ABR-好氧颗粒污泥组合工艺能够有效地处理黄连素制药废水。     

厌氧-好氧工艺处理制药废水的中试研究

将由厌氧折流板反应器(ABR)、移动床生物膜反应器(MBBR)和膜生物反应器(MBR)组合而成的厌氧-好氧工艺用于处理制药废水的中试研究.试验结果表明,当原水SS平均值为1000 mg/L,COD为10 000 mg/L,NH3-N为500 mg/L时,出水浊度、COD和NH3-N分别为3 NTU、500 mg/L以及10 mg/L以下,去除率分别为98%、95%和98%以上.     

ABR+复合人工湿地处理分散性生活污水的中试研究

研究了ABR+复合人工湿地组合工艺处理分散性生活污水的运行效能及ABR中颗粒污泥的特性。结果表明:在pH和温度的范围分别为6.5～8.5,17.0～28.8℃,ABR和复合人工湿地的HRT分别为3 h(容积负荷平均为1.3 kgCOD/(m3.d)及1.3 d(水力负荷平均为24.6 cm/d)的条件下,系统对COD、NH4+-N、TN、TP和浊度均有较好的去除效果,其平均去除率分别为76%、69%、56%、87%和86%,出水浓度平均分别为37 mg/L、2.73 mg/L、6.93 mg/L、0.18 mg/L和5.05 NTU,ABR中形成了性状良好的颗粒污泥。     

微氧条件下厌氧折流板反应器运行特性研究

对厌氧折流板反应器（anaerobic baffled reactor,ABR)在微氧条件下的运行特性进行试验研究，分析了ABR在微氧条件下高效运行的可行性。研究结果表明，适量氧的加入能使ABR的COD去除率提高，出水VFA浓度降低。进水COD为4 000 mg/L,HRT为12 h的相同条件下与厌氧相比，微氧ABR出水COD和VFA浓度的降幅分别为63.7%和66%；微氧ABR内氨氮的去除主要通过同步硝化反硝化和短程硝化反硝化作用；适量氧的加入可以提高微生物的产甲烷活性。     

移动床生物膜反应器—膜生物反应器深度处理模拟废水及工业园区综合废水

将移动床生物膜反应器(MBBR)与膜生物反应器(MBR)有机结合,研究了该MBBR—MBR串联系统在水力停留时间(HRT)为17.50、11.75h条件下的脱碳脱氮的效果以及对工业园区综合废水污染物的去除情况。结果表明:(1)MBBR—MBR串联系统脱碳脱氮的效果良好,HRT的改变对系统的去除效果有一定的影响,随着总HRT由17.50h变为11.75h,模拟废水中COD的去除效果降低,但氨氮、硝态氮和TN的去除效果基本不受影响。(2)MBBR—MBR串联系统处理印染工业园区综合废水也有较好的效果,当进水COD、氨氮分别为150~450、20~40mg/L时,出水COD、氨氮平均分别为53.1、1.8mg/L,MBBR—MBR串联系统对COD、氨氮的去除率平均分别为80.4%、93.1%,但系统对TN的去除效果不是很理想。     

MBBR处理猪场废水厌氧消化液的研究

采用移动床生物膜反应器(MBBR)处理猪场废水厌氧消化液,考察了水力停留时间(HRT),进水COD和NH3-N浓度对反应器处理效果的影响.结果表明,在温度为20～30℃,填料填充比为50%,进水COD和NH3-N浓度分别为1016 mg/L和496 mg/L条件下,当HRT为12.5 h时,COD和NH3-N去除率可分别达到62%和77%,猪场废水厌氧消化液中可生物降解性有机物基本得到去除,当HRT增至23.8 h时,COD和NH3-N去除率分别为64%和86%,出水COD和NH3-N浓度分别为368 mg/L和70 ms/L,均达到了<畜禽养殖业污染物排放标准>(GB18596-2001)的要求.     

Use of diffuse reflectance spectrometry in spot test reactions for quantitative determination of cations in water

Diffuse reflectance spectroscopy can be successfully used for the quantitative determination of small amounts of pollutants like metals. The remission function was found to be linearly proportional to the concentration, when we applied the Kubelka–Munk equation. The color reactions of Cu(II), Co(II), and Ni(II) with dithiooxamide, were realised on filter paper. Reaction between Fe(III) and ammonium thiocyanate was realized on filter paper and gelatine matrix. All measurements were accomplished with a laboratory-constructed reflectometer. We have obtained a calibration curve by plotting the optical density of reflectance A_R vs log of the mol l⁻¹ concentration. Limits of detection at the 10⁻⁴ M level were estimated for all the compounds. Linear dynamic range extend over one order of magnitude and shows the potential of device for the quantitative analysis of environmental pollutants.     

Distribution and sources of polyfluoroalkyl substances (PFAS) in the River Rhine watershed

The concentration profile of 40 polyfluoroalkyl substances (PFAS) in surface water along the River Rhine watershed from the Lake Constance to the North Sea was investigated. The aim of the study was to investigate the influence of point as well as diffuse sources, to estimate fluxes of PFAS into the North Sea and to identify replacement compounds of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA). In addition, an interlaboratory comparison of the method performance was conducted. The PFAS pattern was dominated by perfluorobutane sulfonate (PFBS) and perfluorobutanoic acid (PFBA) with concentrations up to 181 ng/L and 335 ng/L, respectively, which originated from industrial point sources. Fluxes of ΣPFAS were estimated to be ∼6 tonnes/year which is much higher than previous estimations. Both, the River Rhine and the River Scheldt, seem to act as important sources of PFAS into the North Sea.     

BAT and BEP as instruments for reducing emissions of unintentionally produced POPs and development of guidelines under the stockholm convention

The 6th Intergovernmental Negotiating Committee (INC 6), under the Stockholm Convention on POPs, gave an expert group the mandate to develop guidelines for the application and implementation of best available techniques (BAT) and best environmental practices (BEP) for the prevention and reduction of unintentionally produced and emitted POPs, including polychlorinated dibenzodioxins/-furans (PCDD/Fs), polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB). Measures to reduce or eliminate the release of these POPs to the environment can be found in Article 5 of the Convention. BAT and BEP are already being applied as emission reduction instruments in a number of industrialised countries and are elements of other major international treaties, e.g. the UN ECE Protocol on POPs and the Marine Convention's OSPAR and HELCOM, and of the EU Directive for Integrated Pollution Prevention and Control (IPPC Directive). Existing concepts are presented and compared with the requirements of the Stockholm Convention. Consequences, perspectives and questions for the future intersessional work of the above-mentioned Expert Group are discussed.     

Integrative approach to delineate natural attenuation of chlorinated benzenes in anoxic aquifers

Biodegradation of chlorobenzenes was assessed at an anoxic aquifer by combining hydrogeochemistry and stable isotope analyses. In situ microcosm analysis evidenced microbial assimilation of chlorobenzene (MCB) derived carbon and laboratory investigations asserted mineralization of MCB at low rates. Sequential dehalogenation of chlorinated benzenes may affect the isotope signature of single chlorobenzene species due to simultaneous depletion and enrichment of ¹³C, which complicates the evaluation of degradation. Therefore, the compound-specific isotope analysis was interpreted based on an isotope balance. The enrichment of the cumulative isotope composition of all chlorobenzenes indicated in situ biodegradation. Additionally, the relationship between hydrogeochemistry and degradation activity was investigated by principal component analysis underlining variable hydrogeochemical conditions associated with degradation activity at the plume scale. Although the complexity of the field site did not allow straightforward assessment of natural attenuation processes, the application of an integrative approach appeared relevant to characterize the in situ biodegradation potential.     

土壤改良剂对油菜富集238U、226 Ra及232 Th的影响

通过网室盆栽试验,研究了施加磷矿粉(PR)、羟基磷矿粉(HA)、豆渣(SM)、骨碳(BC)及硫酸亚铁等土壤改良剂对油菜(Brassica oleracea L.)自铀矿区污染农田土壤吸收铀(238U)、镭(226Ra)及钍(232Th)的影响.结果表明,不同处理下油菜茎叶对238U、226Ra及232Th的富集系数分别在3.6×10-3～6.2×10-3、6.2×10-3～10.0×10-3及0.9×10-4～2.0×10-4之间.上述不同改良剂处理均能在一定程度上降低植物对238U、226Ra及232Th的吸收,以SM、HA处理效果较显著,其中SM处理下238U、226Ra及232Th的富集系数分别比对照降低42.9%、39%和71%.SM及HA对降低铀矿区污染土壤中植物对上述核素的吸收和富集具有潜在的应用价值.     

硝化速率法用于活性污泥活性测试的研究

以城市污水厂回流污泥中的硝化细菌(氨氧化细菌和亚硝酸盐氧化细菌)为受试生物,HgCl2为标准毒性物质,通过对两组实验--氨氧化速率实验(NH 4-N→NO-2-N)和亚硝酸盐氧化速率实验(NO-2-N→NO-3-N)的研究表明,氨氧化细菌对HgCl2的灵敏度(IC50=0.034 mmol/L)明显高于亚硝酸盐氧化细菌(IC50=0.20 mmol/L).氨氧化速率法测试活性污泥活性时,使用NH 4-N或NO-X-N指标需要120 min或更长的时间,但使用NO-2-N指标仅需30 min就可完成测试,而且结果重现性要比NH 4-N和NO-X-N好,其变异系数CV为5.9 %.     

Polychlorinated dibenzo-p-dioxins and related compounds: the blood levels of young Japanese women.

We investigated PCDDs and related compounds in the blood of young Japanese women, approximately 20 years of age, who had not yet had children, and discussed how the TEQ level of PCDDs and related compounds in their blood may affect the next generation. Means of total TEQ levels were 0.063 pg/g for whole blood basis and 21 pg/g for lipid basis. TEQ of PCDDs, PCDFs and coplanar PCBs accounted for about 43, 34 and 23% of the total TEQ in the whole blood basis, respectively. In the lipid basis, their values were about 44, 34 and 22%, respectively. Previously, we investigated PCDDs and related compounds levels in mother's breast milk, lymphocyte subpopulation and thyroid function of their children, and found negative correlations between the TEQ level of PCDDs and related compounds and CD4+/CD8+, and/or the TEQ level of PCDDs and related compounds and the T₄ level in 36 mothers and children. Of these cases, the average age was approximately 28 years. PCDDs and related compounds may be related to immunopathy, such as atopic dermatitis. The effects of PCDDs and related compounds on babies of young Japanese women are important and must be further evaluated.     

Assessment of Organochlorine Pesticide Residues in Water,Sediment, and Fish of the Songhua River,China

This study examined residual concentrations and associated ecological risks of the organochlorine pesticides (OCPs) hexa- chlorocyclohexane (HCH) and dichloro-diphenyl-trichloroethane (DDT) in water, sediment, and fish of the Songhua River in Zhaoyuan County, China. In June 2012, 10 water, 10 sediment, and 20 fish samples were collected. Residual concentrations of ΣHCH and ΣDDT ranged from 10.0–35.59 ng L^?1 (mean 28.03 ± 11.66 ng L^?1) and 5.12–39.66 ng L^?1 (mean 32.36 ± 11.58 ng L^?1) for water. Residual concentrations of ΣHCH and ΣDDT ranged from 0.52–3.00 ng g^?1 (mean 2.04 ± 0.73 ng g^?1) and 0.34–3.41 ng g^?1 (mean 2.38 ± 0.92 ng g^?1) for sediment. The ratios of α-HCH/γ-HCH were close to 1 at the majority of sampling points, indicating considerable new pollution from the use of lindane. The ratios of p,p′-DDE + p,p′-DDD/ΣDDT were less than 0.5, indicating recent inputs from DDT impurities in dicofol. All HCH and DDT isomers except for p,p′-DDD were detected in fish tissue samples, but the associated ecological risks were estimated to be below levels of concern. The study revealed a historical usage of OCPs in the Zhaoyuan section of the Songhua River and new OCP from the use of lindane and dicofol.     

复配混凝剂理化特性及性能

用聚二甲基二烯丙基氯化铵（PDM）、聚合氯化铝（PAC）按照质量比1%制备了复配混凝剂，研究了其理化特性及原水污染物去除效果。利用Al-Ferron逐时络合比色法研究了复配混凝剂的铝（Ⅲ）形态分布，结果表明，Al_a、Al_b和Al_c分别占12.62%、16.02%和71.36%。复配混凝剂Zeta电位平均值为41.6 mV。红外吸收光谱分析表明复配混凝剂的羟基缔合程度比PAC要高。扫描电镜结果表明，固体复配混凝剂表面较为粗糙、结构疏松。相同投加量时，复配混凝剂对江河水、水库水的浊度、COD_Mn、UV₂₅₄的去除效率均优于PAC。实验利用针杆藻人工模拟高藻原水，当投加PDM：PAC质量比10%的复配混凝剂10 mg/L时，复配混凝剂对藻类的去除率为80.5%。     

Melting and incineration plants of municipal waste. Chemical and biochemical diagnosis of thermal processing samples (emission,residues)

Control of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) in emissions and thermal residues from incinerators has been a cause of public concern for more than one decade. Recently, several studies showed that other persistent organic pollutants (POPs) such as coplanar polychlorinated biphenyls (co-PCBs) also have dioxin-like activity and are released from incinerators. Therefore, the present study was aimed at making a risk assessment about dioxin-like activity in extracts of thermal waste residues (e.g. combustion gas; fly ash, slag) from incineration and melting processes in Germany and Japan. For this purpose, polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs), coplanar polychlorinated biphenyls (co-PCBs), polychlorinated naphthalenes (PCNs) and polyaromatic hydrocarbons (PAHs) were analyzed by chemical analysis. Additionally, 2, 3, 7, 8-TCDD equivalents (EROD-TEQs) were determined by in vitro Micro-EROD bioassay using rat H4IIE hepatoma cells. EROD-TEQs could be correlated to I-TEQ values (from PCDD/Fs/co-PCBs) analyzed by chemical analysis resulting in a maximal sixfold higher estimate. Our study indicates minor influences of co-PCBs, PAHs and PCNs to the sum of dioxin-like toxicity in the extracts of thermal waste residues as determined here. Furthermore, we showed that the levels of dioxins and co-PCBs contained in slag from melting processes and bottom ashes from incineration processes were lower by 1-2 orders of magnitude than that in fly ash.