铁碳微电解法预处理垃圾渗滤液膜滤浓缩液

对垃圾渗滤液膜滤浓缩液采用铁碳微电解法进行预处理,探讨了p H值、反应时间及气液比对COD去除效率的影响。结果表明,当p H值为3、反应时间120 min、气液比10∶1时,COD、TN的去除率分别为79.6%,56.4%;NH3-N由进水的70.9 mg/L上升为77.0 mg/L;预处理效果较好。但是由于铁碳微电解对盐度没有去除效果,影响后续反应进行。如何经济有效地降低含盐量成为今后研究重点。     

铁碳微电解法预处理猪场沼液中氨氮的研究

铁碳微电解是新型的污水处理技术,为了研究猪场沼液中氨氮的去除,将铁碳微电解技术应用于预处理难降解的厌氧沼液中的氨氮。经预先浸泡处理后的铁碳已达到吸附饱和,以此铁碳材料,分别采用了单因素实验和正交试验,用可见光分光光度法测试氨氮的浓度。单因素实验确定了铁碳微电解法影响氨氮去除的因素,选取pH值、反应时间、铁碳比为正交试验因素,通过正交试验得到,当温度为(20±1)℃,铁碳比为1∶1,pH值为3,反应时间为60 min时去除氨氮的效果最好,去除率为34.01%。铁碳微电解法预处理猪场沼液有一定的应用前景。     

木兰县饮用水源地水质状况分析研究

2012年木兰县监测站对木兰县饮用水源地水质状况进行了监测,监测了六项常规的监测项目,其中包括:pH、总硬度、铁、锰、浑浊度、总大肠菌群.通过这些监测数据可知,木兰县饮用水源地中pH、总硬度、浑浊度均能达到中国《生活饮用水卫生标准》和国家《地下水质量标准》(GB 14848-93)规定,总大肠菌群四个季度均未检出,但铁的含量在第三季度出现超标情况,锰的含量在第一、二、三季度出现超标,本文分析了超标的成因及处理的方法,并提出建议.     

钢铁工业氮氧化物污染防治途径研究

针对钢铁工业氮氧化物减排的紧迫形势,首先介绍了钢铁工业氮氧化物主要排放源,提出了烧结工序和自备电厂是氮氧化物排放的主要污染源,其烟气中氮氧化物控制是钢铁企业氮氧化物减排的重点;其次对钢铁工业氮氧化物生成机理,热力型、燃料型、快速型进行了分析;在此基础上,总结了钢铁工业烧结、自备电厂、焦化、炼铁、轧钢工序氮氧化物污染防治技术途径,为钢铁工业进一步开展氮氧化物减排工作提供了技术支撑.     

Modulation-assisted high speed machining of compacted graphite iron (CGI)

The application of controlled, low-frequency modulation (～100 Hz) superimposed onto the cutting process in the feed-direction – modulation-assisted machining (MAM) – is shown to be quite effective in reducing the wear of cubic boron nitride (CBN) tools when machining compacted graphite iron (CGI) at high machining speeds (>500 m/min). The tool life is at least 20 times greater than in conventional machining. This significant reduction in wear is a consequence of the multiple effects realized by MAM, including periodic disruption of the tool–workpiece contact, formation of discrete chips, enhanced fluid action and lower cutting temperatures. The propensity for thermochemical wear of CBN, the principal wear mode at high speeds in CGI machining, is thus reduced. The tool wear in MAM is also found to be smaller at the higher cutting speeds (730 m/min) tested. The feed-direction MAM appears feasible for implementation in industrial machining applications involving high speeds.     

Fe2+和Fe3+对厌氧氨氧化污泥活性的影响

通过接种厌氧氨氧化污泥研究了Fe离子浓度及价态变化对厌氧氨氧化污泥活性的影响.短期浓度影响结果表明,当进水铁离子浓度由0升高到5 mg·L-1时,厌氧氨氧化污泥活性因受刺激而逐渐增强;当进水铁离子浓度大于5 mg·L-1时,因厌氧氨氧化反应产碱,铁离子形成氢氧化物沉淀,生物活性未受到影响.不同价态铁离子浓度变化对厌氧氨氧化污泥活性的影响无明显区别.长期价态影响结果表明,经过71个周期培养,含Fe2+进水的厌氧氨氧化反应器R1脱氮效能(以氮计)由0.28 kg·(m3·d)-1升高到0.65 kg·(m3·d)-1,是含Fe3+进水反应器R2的1.28倍.因此Fe2+更适合厌氧氨氧化菌生长的需求.实验结果进一步表明,Fe3+易导致厌氧氨氧化反应器R2内氨氮过量转化,亚硝氮与氨氮转化比(1.17)明显低于含Fe2+进水的反应器R1内亚硝氮与氨氮转化比(1.24).     

地下水中常见离子对纳米零价铁除Se（Ⅳ）动力学的影响

采用间歇实验对纳米零价铁(nZVI)除四价硒(Se(Ⅳ))进行实验性研究,考察了地下水中共存离子对nZVI除Se(Ⅳ)动力学的影响.结果表明,在厌氧条件下,当nZVI投加量为0.1 g·L-1,Se(Ⅳ)浓度为100μmol·L-1,NaCl浓度为0.01 mol·L-1,pH=7.0,T=25℃±1℃时,投加CO2-3或SO2-4浓度为1 mmol·L-1、腐殖酸(humic acid,HA)为5 mg·L-1时,明显抑制了Se(Ⅳ)的去除.投加0.5 mmol·L-1Ca2+或Mg2+时,对除Se(Ⅳ)影响不大;而Ca2+(3 mmol·L-1)、Mg2+(3 mmol·L-1)时,Se(Ⅳ)的去除效率明显下降.未加共存离子时,Se(Ⅳ)在20 min时基本去除完,共存离子存在的情况下,nZVI对Se(Ⅳ)的去除率在30 min时达到100%.反应过程中二价铁(Fe2+)随着Se(Ⅳ)的去除趋于平稳.ORP在反应过程中快速从正值下降至负值,由此说明nZVI除Se(Ⅳ)的过程发生了还原反应.     

Remediation of alachlor and atrazine contaminated water with zero-valent iron nanoparticles

Zero-valent iron nanoparticles (nZVI, diameter < 90 nm, specific surface area = 25 m² g^?1) have been used under anoxic conditions for the remediation of pesticides alachlor and atrazine in water. While alachlor (10, 20, 40 mg L^?1) was reduced by 92–96% within 72 h, no degradation of atrazine was observed. The alachlor degradation reaction was found to obey first-order kinetics very closely. The reaction rate (35.5 × 10^?3–43.0 × 10^?3 h^?1) increased with increasing alachlor concentration. The results are in conformity with other researchers who worked on these pesticides but mostly with micro ZVI and iron filings. This is for the first time that alachlor has been degraded under reductive environment using nZVI. The authors contend that nZVI may prove to be a simple method for on-site treatment of high concentration pesticide rinse water (100 mg L^?1) and for use in flooring materials in pesticide filling and storage stations.     

铁炭复配修复地下水中NO_3~--N的条件研究

采用了铁炭复配修复地下水中NO3--N,探讨了实验条件对修复效果的影响。结果表明,在pH值近中性条件(初始pH 6.42)下,反应时间为1 h时NO3--N修复率达到60.85%;Fe/C=1∶1时介质最佳用量分别为4~5 g;Fe/C=1/1.5时修复率为72.80%;反应速率在高振荡强度下大于低振荡强度;氧化铜的催化效果最好,可使修复率提高7.5个百分点。铁炭复配介质修复地下水中NO3--N是有效可行的,修复率随反应时间的增加而提高,在Fe/C=1∶1时修复率与介质用量呈正相关,无限减小Fe/C比并不能无限提高修复率,振荡强度对修复具有显著影响,低振荡强度下的修复过程较高强度存在滞后现象,并非所有金属氧化物催化剂对铁炭修复NO3--N均有促进作用。     

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.