Roles of manganese oxides in degradation of phenol under UV-Vis irradiation: Adsorption, oxidation, and photocatalysis

The effect of crystal structure on photocatalytic activities of manganese oxides and underlying reaction mechanism were investigated.     

中心组合设计优化S-Cr-TiO2催化剂光降解工艺条件

在确定的温度和光照条件下,采用中心组合设计法研究了固相反应法合成的硫与铬共掺杂二氧化钛(S-Cr-TiO2)光催化剂与水溶苯胺蓝(ANB)可见光降解过程中的三个作用因子:催化剂的浓度、水溶苯胺蓝水溶液的pH值及其初始浓度之间的相互作用关系,得到了影响因子与降解速率之间的回归方程及因素之间相互作用的响应面图.结果表明,S...     

等离子体催化降解有机废水研究

研究了多种因素对高压脉冲介质阻挡放电低温等离子体法处理印染废水效果的影响。通过实验得出结论:随着有效处理时间和峰值外施电压的增加,废水中的有机物的去除率增加;随着水样浓度的增加,废水中有机物的去除率降低;随着催化剂(TiO)2量的增加,废水中有机物的去除率先升高后降低,最佳催化剂的加入量为0.5 g/L TiO2悬浮液0.5 mL。     

纳米零价铁铜双金属对铬污染土壤中Cr(Ⅵ)的还原动力学

采用液相还原法制备纳米零价铁铜双金属(n ZVI/Cu),通过扫描电子显微镜(SEM)和X射线衍射(XRD)对其进行形貌观测和表征分析,用制备的n ZVI/Cu修复Cr(Ⅵ)污染的土壤,研究了不同反应条件对修复效果的影响,探讨了还原动力学规律.结果表明,n ZVI/Cu对土壤中的Cr(Ⅵ)有很好的降解效果,反应初始p H为7,温度为30℃时,加入2 g·L~(-1)的n ZVI/Cu材料,在10 min内Cr(Ⅵ)含量为88 mg·kg~(-1)的污染土壤中的Cr(Ⅵ)去除率可以达到99%以上.改变n ZVI/Cu加入量、p H值、反应温度以及添加腐殖酸都会对Cr(Ⅵ)的去除效果产生影响.改变p H值和反应温度对去除土壤中Cr(Ⅵ)的影响都比较明显,p H值越小,反应温度越高Cr(Ⅵ)的去除效果越好,添加腐殖酸对去除土壤中的Cr(Ⅵ)有一定的影响.n ZVI/Cu降解Cr(Ⅵ)的过程符合伪一级还原动力学模型,还原速率与反应温度的关系符合阿仑尼乌斯(Arrhenius)定律,反应活化能Ea为104.26 k J·mol~(-1).     

Reaction mechanism and metal ion transformation in photocatalytic ozonation of phenol and oxalic acid with Ag+/TiO2

Photocatalytic ozonation of phenol and oxalic acid （OA） was conducted with a Ag^＋/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag^＋ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger. It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag＋ was easily reduced and deposited on the surface of Tit2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag^＋ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants.     

Ultrasonic preparation of nano-nickel/activated carbon composite using spent electroless nickel plating bath and application in degradation of 2,6-dichlorophenol

Ni was effectively recovered from spent electroless nickel （EN） plating baths by forming a nano-nickel coated activated carbon composite. With the aid of ultrasonication, melamine- formaldehyde-tetraoxalyl-ethylenediamine chelating resins were grafted on activated carbon （MFT/AG）. PdC12 sol was adsorbed on MFT/AC, which was then immersed in spent electroless nickel plating bath; then nano-nickel could be reduced by ascorbic acid to form a nano-nickel coating on the activated carbon composite （Ni/AC） in situ. The materials present were carefully examined by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectroscopy and electro- chemistry techniques. The resins were well distributed on the inside and outside surfaces of activated carbon with a size of 120 ± 30 nm in MFT/AC, and a great deal of nano-nickel particles were evenly deposited with a size of 3.8 ± 1.1 nm in Ni/MFT. Moreover, Ni/AC was successfully used as a catalyst for ultrasonic degradation of 2.6-dichloronhenol.     

Photocatalytic activity of Fe-doped CaTiO3 under UV-visible light

The photocatalytic degradation of methylene blue（MB） over Fe-doped CaTiO3 under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction（XRD）, scanning electron microscope（SEM） equipped with an energy dispersive spectrometer（EDS） system, Fourier transform infrared spectra（FT-IR）, and UV-visible diffuse reflectance spectroscopy（DRS）. The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO3 in the visible light region. The Fe-doped CaTiO3 exhibited higher photocatalytic activity than CaTiO3 for the degradation of MB.However, the photocatalytic activity of the Fe-doped CaTiO3 was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO3 prepared at500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB（10 ppm）under UV-visible light for 180 min.     

贫营养条件下17β-雌二醇厌氧生物降解规律研究

17β-雌二醇作为环境甾体雌激素污染的主要污染物之一,广泛分布于自然环境中。采用批次实验,研究了在贫营养条件下17β-雌二醇厌氧生物降解规律。结果表明,在贫营养条件下,厌氧污泥对17β-雌二醇的去除率达到90%(35℃,76 d),且降解作用主要集中在快速降解阶段,降解规律符合一级降解动力学模型(R2=0.95);厌氧污泥对17β-雌二醇的去除主要是通过转化为雌性效力较低的雌酮,再由雌酮转化为其他的转化产物,如17α-雌二醇;Fe(Ⅲ)对17β-雌二醇的去除和转化没有显著的影响。接种污泥的内源代谢作用产生甲烷,Fe(Ⅲ)的存在可以提高甲烷的产率,但对甲烷的总量没有显著影响。     

厌氧共代谢分解难降解有机物的研究进展

文章介绍了厌氧共代谢的提出、作用机制、调控研究及应用现状,从共代谢技术的基质类型、菌群结构和代谢途径三方面综述了国内外有关厌氧共代谢作用机制的研究现状、发展趋势,并着重分析了厌氧共代谢的调控技术和应用情况,展望了厌氧共代谢技术的未来研究方向,为解决难降解有机污染物的治理瓶颈提供借鉴和参考。     

农田土壤酞酸酯的生物降解及真菌生长动态试验研究

室内模拟研究了农田土壤中酞酸酯(PAEs)含量、土壤基础呼吸量和真菌数量在PAEs降解过程中的变化。试验设对照(CK)、接种(JZ)和补种(BZ)3种处理,补接种的PAEs降解真菌(棒束梗霉属F3、芽枝状枝孢F4和爪哇正青霉F9)以每种2%的接种量加入土中,补种量与接种量相同,补种周期为20 d。结果表明,3种处理对土壤PAEs都有一定的降解作用,但接种和补种处理的土壤中4种复合PAEs总降解率分别比对照处理高出46.53%和51.54%。在试验周期内,补种处理的土壤麦角固醇含量维持在2.5~3.0μg/g,表明真菌数量稳定,而对照处理的土壤麦角固醇含量表现为先升高随后逐渐降低的趋势,60 d时下降到1.9μg/g;3种处理的土壤基础呼吸量也均呈下降趋势。因此,接种真菌可提高土壤PAEs的降解效率,而补种措施是保持土壤中真菌数量稳定的有效方法。