土壤胡敏素对铜离子的吸附作用及其机理研究

以暗棕壤为供试土壤,研究了不同溶液pH值、离子强度、接触时间、反应温度和初始铜离子(Cu~(2+))浓度条件下,胡敏素对Cu~(2+)的吸附作用;利用扫描电子显微镜(SEM)、X-射线能量色散谱(EDS)、傅立叶变换红外光谱(FTIR)和X-射线光电子能谱(XPS),对胡敏素/胡敏素-Cu~(2+)复合物的表面形貌、元素分布和官能团组成进行了分析;应用延展X-射线吸收精细结构谱(EXAFS),对吸附态Cu~(2+)的局域配位结构进行了表征.结果表明:胡敏素对Cu~(2+)的吸附量随pH值、接触时间、反应温度和Cu~(2+)浓度的增加而增加,但随离子强度的增加而下降;吸附动力学符合准二级动力学方程,而吸附等温线用Langmuir方程的拟合效果较好;吸附过程需要能量,是自发、吸热和自由度增加的缔合反应;吸附Cu~(2+)之后,胡敏素表面产生了团聚现象,表面羧基、羟基、吡啶氮和N—O基团参与了Cu~(2+)的吸附作用,同时吸附态Cu~(2+)是以内层配位形式与胡敏素表面的O/N和C原子结合.     

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.     

Synthesis of novel CeO2-BiVO4/FAC composites with enhanced visible-light photocatalytic properties

To utilize visible light more effectively in photocatalytic reactions, a fly ash cenosphere （FAC）-supported CeO2-BiV04 （CeO2-BiVO4/FAC） composite photocatalyst was prepared by modified metalorganic decomposition and impregnation methods. The physical and photophysical properties of the composite have been characterized by X-ray diffraction （XRD）, scanning electron microscope （SEM） and energy dispersive X-ray spectroscopy （EDX）, X-ray photoelectron spectroscopy （XPS）, and UV-Visible diffuse reflectance spectra. The XRD patterns exhibited characteristic diffraction peaks of both BiVO4 and Ce02 crystalline phases. The XPS results showed that Ce was present as both Ce4＋ and Ce3＋ oxidation states in Ce02 and dispersed on the surface of BiV04 to constitute a p-n heterojunction composite. The absorption threshold of the CeO2-BiVO4/FAC composite shifted to a longer wavelength in the UV-Vis absorption spectrum compared to the pure Ce02 and pure BiV04. The composites exhibited enhanced photocatalytic activity for Methylene Blue （MB） degradation under visible light irradiation. It was found that the 7.5 wt.% CeO2-BiVO4/FAC composite showed the highest photocatalytic activity for MB dye wastewater treatment.     

Graphene-supported nanoscale zero-valent iron：Removal of phosphorus from aqueous solution and mechanistic study

Excess phosphorus from non-point pollution sources is one of the key factors causing eutrophication in many lakes in China,so finding a cost-effective method to remove phosphorus from non-point pollution sources is very important for the health of the aqueous environment. Graphene was selected to support nanoscale zero-valent iron(nZVI)for phosphorus removal from synthetic rainwater runoff in this article. Compared with nZVI supported on other porous materials,graphene-supported nZVI(G-nZVI) could remove phosphorus more efficiently. The amount of nZVI in G-nZVI was an important factor in the removal of phosphorus by G-nZVI,and G-nZVI with 20 wt.% nZVI(20% G-nZVI)could remove phosphorus most efficiently. The nZVI was very stable and could disperse very well on graphene,as characterized by transmission electron microscopy(TEM) and scanning electron microscopy(SEM). X-ray photoelectron spectroscopy(XPS),Fourier Transform infrared spectroscopy(FT-IR) and Raman spectroscopy were used to elucidate the reaction process,and the results indicated that Fe-O-P was formed after phosphorus was adsorbed by G-nZVI. The results obtained from X-ray diffraction(XRD) indicated that the reaction product between nZVI supported on graphene and phosphorus was Fe3(PO4)2·8H2O(Vivianite). It was confirmed that the specific reaction mechanism for the removal of phosphorus with nZVI or G-nZVI was mainly due to chemical reaction between nZVI and phosphorus.     

PM2.5监测市场暗战 国货何时能扬眉吐气?

小余是国内一在环境空气自动监测系统领域颇有口碑的厂家驻安徽办事处的代表。自2011年以来,他就不断游走于各地环保局之间,打听留意各种采购PM2.5监测设备的信息,以期抢得先机。5月10日,周末,在合肥一咖啡厅,他在向本刊记者回顾两年来的心路历程时,更多地是在用"起个大早却赶了个晚集"一词来形容。     

污水厂二级出水中难凝聚有机物的臭氧化特性

以城市污水处理厂二级出水为原水,研究臭氧化处理对水中难凝聚有机物的去除效果.结果表明单独混凝对水中有机物的去除率较低,混凝过程中未被去除的有机物属于难凝聚有机物,加入臭氧进行氧化,随着臭氧投加量的增加,二级出水色度和UV254去除率逐渐增大,而DOC去除率变化较小.当臭氧投加量(以O3/DOC计)增加至1.5 mg·mg-1时,色度、UV254和DOC的去除率分别为45%、34%和20%,说明臭氧易于与不饱和结构有机物反应,而直接氧化的矿化能力较弱.为进一步明确二级出水有机物种类和含量的变化,测定了混凝和不同臭氧投加量下有机物的相对分子质量和三维荧光光谱.结果表明混凝对有机物含量的影响很小,而臭氧能够优先氧化分解难凝聚有机物中的大分子物质,明显减弱腐殖质类物质的荧光峰强度,但不改变荧光峰位置.同时采用光电子能谱分析有机物结构的变化规律,结果表明混凝能够去除含羧基类官能团有机物,而臭氧则易于与含苯环类难凝聚有机物反应,随着臭氧投加量的增大,脂肪类饱和有机物含量有所升高.     

外绝缘用液体硅橡胶老化现象的微观表征

本文针对近年来出现在一些变电站SF6电压、电流互感器的液体硅橡胶绝缘护套出现龟裂老化这一现象,对发生老化的硅橡胶材料进行了性能测试和试验,并利用红外光谱分析、XPS分析、热失重等手段分析了其微观结构和物质组成的变化。研究发现老化后的液体硅橡胶中Si-C、Si-O官能团和Si、C、O元素的相对含量发生了变化,且随着老化程度的增加呈现出较为明显的规律,老化越严重,Si-C键含量越少,C元素的含量越少,O元素含量越多。本文认为,用官能团含量、元素相对含量可以准确地表征液体硅橡胶材料的老化程度。通过对不同老化程度的液体硅橡胶进行的憎水性、耐漏电起痕性能的试验也证实了本文的观点。     

Cation exchange resin supported nanoscale zero-valent iron for removal of phosphorus in rainwater runoff

Self-made cation exchange resin supported nanoscale zero-valent iron （R-nZVI） was used to remove phosphorus in rainwater runoff. 80% of phosphorus in rainwater runoff from grassland was removed with an initial concentration of 0.72 mg. L-1 phosphorus when the dosage of R-nZVl is 8 g per liter rainwater, while only 26% of phosphorus was removed when using cation exchange resin without supported nanoscale zero-valent iron under the same condition. The adsorption capacity of R-nZVI increased up to 185 times of that of the cation exchange resin at a saturated equilibrium phosphorous concentration of 0.42 mg. L-1. Various techniques were implemented to characterize the R-nZVI and explore the mechanism of its removal of phosphate. Scanning electron microscopy （SEM） indicated that new crystal had been formed on the surface of R-nZVI. The result from inductive coupled plasma （ICP） indicated that 2.1% of nZVI was loaded on the support material. The specific surface area was increased after the load of nanoscale zero-valent iron （nZVI）, according to the measurement of BET-N2 method. The result of specific surface area analysis also proved that phosphorus was removed mainly through chemical adsorption process. X-ray photoelectron spectroscopy （XPS） analysis showed that the new product obtained from chemical reaction between phosphate and iron was ferrous phosphate.     

生物矿化针铁矿吸附铬的机理探讨

针铁矿在自然界中广泛存在,对重金属离子在地表的迁移和转化有重要影响.利用天然生物矿化针铁矿进行了Cr(Ⅲ)吸附研究,并利用扫描电子显微镜(SEM)和X射线光电子能谱(XPS)等对吸附后的样品进行表征,发现样品中铬的含量随着Al2O3含量的增加而增加,说明表面带负电荷的含高岭土等的粘土较针铁矿对Cr(Ⅲ)有更强的吸附能力.样品的XPS研究表明,NO3-也参与了反应,且促进了Cr(Ⅲ)的氧化.研究还发现,Cr(Ⅲ)在针铁矿上的吸附不均匀,与文献报道的情况不同.     

Shewanella oneidensis MR-1和Shewanella putrefaciens对V(V)的还原及其影响因素

在实验室模拟培养条件下,研究Shewanella oneidensis MR-1和Shewanella putrefaciens在厌氧体系中对V（V）的耐性试验,探讨在不同的V（V）浓度、接菌量、pH值和不同蒽醌-2,6-二磺酸（AQDS）浓度下对V（V）还原的影响,并通过扫描电镜（SEM）和X射线光电子能谱（XPS）进行表征.结果表明V（V）浓度低于10mg/L时对S.oneidensis MR-1和S.putrefaciens的生长影响较小,V（V）浓度超过20mg/L则会抑制其生长和V（V）的还原;随着接菌量的增加,2种微生物对V（V）的还原能力逐渐增强;2种微生物最适生长pH值均为7.0左右,弱碱性环境下2种微生物对V（V）的还原率高于弱酸性环境;添加1mmol/L AQDS会加快2种微生物对V（V）的还原.菌株培养3d后通过SEM分析,S.oneidensis MR-1和S.putrefaciens进行V（V）还原的同时也伴有少量的吸附作用.利用XPS能谱分析表明S.oneidensis MR-1和S.putrefaciens将V（V）还原为V（IV）.