Fenton氧化-序批式膜生物反应器耦合处理干法腈纶废水

采用Fenton氧化-序批式膜生物反应器(SBMBR)组合工艺处理干法腈纶废水。结果表明,在废水初始pH值为3.0,H2O2投加量为90.0 mmol/L,Fe2+投加量为20.0 mmol/L,反应时间为2.0 h的条件下,Fenton氧化预处理对腈纶生产废水的COD去除率达到47.0%以上,COD由1 091 mg/L降至560 mg/L,废水的BOD5/COD由0.32升至0.69,废水的可生化性得到显著提高。Fenton处理出水与丙烯腈废水等比例混合后,采用SBMBR进行生化处理,在水力停留时间为24 h,90 min缺氧/150 min好氧交替运行的条件下,COD、NH4+-N和TN的平均去除率分别为71.7%、97.2%和47.4%,碳源不足是限制TN去除效果的主要影响因素。在无外加碳源的条件下,组合工艺处理后出水COD和NH4+-N浓度分别为117 mg/L和1.7 mg/L,出水水质可以稳定达到国家一级排放标准(GB8978-1996)。     

无机陶瓷膜处理油田采出水

针对陶瓷膜在油田采出水处理过程中操作参数的选择及污染机理进行了研究。通过现场实验,分析了不同的操作参数对膜通量的影响,陶瓷膜对含油量及悬浮物的去除效果,膜阻力组成及膜污染清洗方法。实验结果表明,在确定出水水质达到低渗透油田注水水质A1级标准条件下,陶瓷膜过滤最佳操作条件为:跨膜压差0.16 MPa、温度50℃、膜面流速5.0 m/s。同时发现,NaOH和HNO3联合清洗有助于恢复膜通量。     

MFC-MBR耦合系统运行效果

膜生物反应器(MBR)是一种高效的污水处理工艺,而微生物燃料电池(MFC)能有效降解污泥中的胞外生物有机质(EBOM)并回收电能.将MFC与MBR联用,建立了一套能够有效抑制膜污染同时回收电能的新系统——MFC-MBR耦合系统,MBR的剩余污泥经MFC处理后回流.以传统MBR为对照,对耦合系统中污水处理效果、膜污染情况和污泥混合液的性质进行研究.研究表明,耦合系统的污水处理效果没有明显恶化,COD去除率为94％,NH4+-N的去除率为92％.耦合系统能够有效减缓膜污染的发生,清洗周期延长了28％.污泥混合液的MLVSS/MLSS稳定在80％ ～ 88％,系统内几乎没有无机颗粒积累.松散结合态胞外聚合物(LB-EPS)降低了48％,使污泥混合液性质得到改善.较低的污泥比阻(2.69×1012m/kg)和标准化毛细吸水时间(1.67 s·L/g MLSS),证明耦合系统污泥混合液脱水性能提高了.     

乳状液膜法处理煤制兰炭废水

以磷酸三丁酯(TBP)为载体、煤油为膜溶剂、NaOH水溶液为内水相,采用乳状液膜法处理兰炭废水。实验结果表明:当TBP体积分数为4%、表面活性剂质量分数为4%、内水相NaOH质量分数为12%、油内比(乳状液的油相与内水相的体积比)为3∶2、乳水比为1∶5、萃取时间为15min时,废水中的酚类(以苯酚计)去除率达到85%以上,COD去除率达83%以上。     

Mobile passive samplers: concept for a novel mode of exposure

Integrative passive sampling with devices such as semipermeable membrane devices generally relies on rigs for month-long static exposures in water. We evaluate here whether mobile exposures of passive samplers can provide reliable estimates of dissolved contaminant concentrations. Mobile exposures were obtained by towing samplers fastened to the end of a benthic trawl net. Significant and reproducible absorption of polycyclic aromatic hydrocarbons during 5 h-long deployments was made possible by high sampling rates resulting from high water turbulences during towing at 1.2-1.5 knots. Sampling rates (72-215 L d⁻¹) estimated from the dissipation of performance reference compounds were supported by in situ calibration with samplers exposed for a 30 days in the vicinity of the test site. Higher fluoranthene and pyrene absorption in samplers exposed to the trawling-induced sediment plume could be attributed to desorption from re-suspended sediments. This mode of exposure has the potential to be used in monitoring programmes.     

PVC/PES-g-PEGMA共混膜的制备及其耐污染性能

首先将聚乙二醇单甲基甲醚酯(PEGMA)接枝到聚醚砜(PES)上得到PES-g-PEGMA,然后利用溶液共混的方法,将聚氯乙烯(PVC)与PES-g-PEGMA共混,通过溶剂-非溶剂扩散诱导相分离法(NIPS)制备PVC/PES-g-PEGMA共混膜。在此基础上对PVC/PES-g-PEGMA共混膜的断面和表面微观结构、水通量、截留率、机械性能及耐污染等性能进行测试,并采用接触角,含水率(EWC),X射线光电子能谱仪(XPS)来表征PES-g-PEGMA的质量百分含量对PVC/PES-g-PEGMA共混膜亲水性的影响。结果表明,PVC/PES-g-PEGMA共混膜水通量,亲水性较纯PVC有很大程度的提高。耐污染性实验表明,随着PES-g-PEGMA的增加,耐污染性逐渐增强。实验结果同时也表明,该共混体系最佳共混比为7∶3。     

电镀综合废水对DF膜的污染

江苏某电镀厂的电镀综合废水在采用DF膜进行预处理时,膜易受到污染。针对这一问题,采用DF膜生产厂家提供的小试装置,研究探索了膜污染的原因及其具体特征。实验结果表明,在处理电镀综合废水时,DF膜的污染速率较快,而酸洗对DF膜的恢复性较好,研究还证实电镀综合废水中的无氰沉锌水洗液是造成DF膜污染的主要原因。     

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.     

Determination of organochlorine and organophosphate pesticide residues in fruits,vegetables and sediments

Abstract

A method is described for the determination of organochlorine and organophosphate pesticide residues in fruits, vegetables and sediments. The concentrated solvent extract was sealed in a polymeric membrane tube, dialysed in cyclohexane and the solvent replaced with hexane. The organophosphates were analysed on a specific thermionic detector without further clean‐up. For the organochlorine pesticides the extract was eluted through 3 g of alumina and analysed on GC/ECD. The clean‐up for sediment extract was carried out on a10 g alumina column with 100 mL hexane containing 5% acetone and the eluate was concentrated to 5 mL.

The detection limit for organophosphates on a 40 g sample and a final volume of 10 mL was on the average 0.01 mg/kg. The detection limit for organochlorine pesticides, with the final volume of 25 mL, was 0.005 mg/kg for all pesticides except for p,p'‐DDT and endosulfan sulphate, which was 0.01 mg/kg.

The detection limit for oganochlorine pesticides in sediment, with the final volume of 2 mL, was less than 1 μg/kg and for organophosphate pesticides less than 10 μg/kg when the final volume was made to 0.5 mL. At the detection limits the method produced a very high coefficient of variation for both organochlorine and organophosphate pesticides.     

Genotoxicity of chromium in vitro on yeast: Interaction with DNA†

The genotoxicity of chromium chloride was investigated in cells of D₇ strain of Saccharomyces cerevisiae harvested either from logarithmic or stationary growth phase.

A weak induction of mifotic gene conversion and point reverse mutation was obtained when the incubations were performed using phosphate buffer. No genetic effect was observed when the incubations were performed using Tris‐HCl buffer.

The experiments with ⁵¹Cr radiotracer demonstrated that Cr³⁺ ion enters the yeast cells and binds to DNA even if the incubation mixture was performed with Tris HCl buffer. This behaviour could be due to the highest concentration of CrCl₃ that cause some damages to cytoplasmatic membrane.