铁锰复合氧化物同时吸附锑镉性能研究

以五价锑（Sb（V））和镉（Cd²⁺）为对象,考察了二者单独存在和共存体系下铁锰复合氧化物（FMBO）对其吸附性能,探讨了Sb（V）（或Cd²⁺）的吸附对Cd²⁺（或Sb（V））吸附的影响.研究发现,单独存在体系下Sb（V）和Cd²⁺的吸附常数K_F分别为0.48和1.13 L·mg^-1,而共存体系下则分别提高至1.88和1.51 L·mg^-1;Elovich动力学模型可较好地描述共存条件下Cd²⁺与Sb（V）在FMBO表面的吸附,表明该体系的吸附为多层吸附且为非均相扩散过程;吸附48 h后Sb（V）和Cd²⁺的最大吸附量分别达到0.32和1.43 mmol·g^-1;Sb（V）在偏酸性而Cd²⁺在偏碱性pH范围具有较好的吸附效果.Sb（V）（或Cd²⁺）通过改变FMBO表面ζ电位和反应平衡pH等机制影响Cd²⁺（或Sb（V））的吸附.此外,XPS和吸附后水相铁锰浓度结果显示,Cd²⁺可能与FMBO体相中Mn²⁺进行晶格置换并促进Mn²⁺的溶出,进而促进了Sb（V）的吸附.     

Synthesis of a novel ternary HA/Fe-Mn oxides-loaded biochar composite and its application in cadmium(II) and arsenic(V) adsorption

Cadmium (Cd) and arsenic (As) are two of the most toxic elements. However, the chemical behaviors of these two elements are different, making it challenging to utilize a single adsorbent with high adsorption capacity for both Cd(II) and As(V) removal. To solve this problem, we synthesized HA/Fe-Mn oxides-loaded biochar (HFMB), a novel ternary material, to perform this task, wherein scanning electron microscopy (SEM) combined with EDS (SEM-EDS) was used to characterize its morphological and physicochemical properties. The maximum adsorption capacity of HFMB was 67.11?mg/g for Cd(II) and 35.59?mg/g for As(V), which is much higher compared to pristine biochar (11.06?mg/g, 0?mg/g for Cd(II) and As(V), respectively). The adsorption characteristics were investigated by adsorption kinetics and the effects of the ionic strength and pH of solutions. X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FT-IR) revealed that chelation and deposition were the adsorption mechanisms that bound Cd(II) to HFMB, while ligand exchange was the adsorption mechanism that bound As(V).     

Ultrasensitive and selective 4-aminophenol chemical sensor development based on nickel oxide nanoparticles decorated carbon nanotube nanocomposites for green environment

Nickel oxide nanoparticles decorated carbon nanotube nanocomposites(Ni O·CNT NCs)were prepared in a basic medium by using facile wet-chemical routes. The optical,morphological, and structural properties of Ni O·CNT NCs were characterized using Fourier transformed infra-red(FT-IR), Ultra-violet visible(UV/Vis) spectroscopy, field-emission scanning electron microscopy(FESEM), X-ray energy dispersed spectroscopy(XEDS), X-ray photoelectron spectroscopy(XPS), and powder X-ray diffraction(XRD) methods. Selective4-aminophenol(4-AP) chemical sensor was developed by a flat glassy carbon electrode(GCE, surface area: 0.0316 cm~2) fabricated with a thin-layer of NCs. Electrochemical responses including higher sensitivity, large dynamic range(LDR), limit of detection(LOD), and long-term stability towards 4-AP were obtained using the fabricated chemical sensors. The calibration curve was found linear(R~2= 0.914) over a wide range of 4-AP concentration(0.1 nmol/L–0.1 mol/L). In perspective of slope(2 × 10~(-5)μA/μM), LOD and sensitivity were calculated as 15.0 ± 0.1 pM and ~ 6.33 × 10~(-4)μA/(μM·cm) respectively. The synthesized Ni O·CNT NCs using a wet-chemical method is a significant route for the development of ultrasensitive and selective phenolic sensor based on nano-materials for environmental toxic substances. It is suggested that a pioneer and selective development of 4-AP sensitive sensor using Ni O·CNT NCs by a facile and reliable current vs voltage(I–V)method for the major application of toxic agents in biological, green environmental, and health-care fields in near future.     

Dynamic changes of microbial community diversity in a photohydrogen producing reactor monitored by PCR-DGGE

A PCR-DGGE (denaturing gradient gel electrophoresis of polymerase chain reaction) protocol was used for monitoring the dynamic changes in the microbial population during photohydrogen production. Total DNA was extracted directly from the mixed bacterial community in the reactor and subjected to PCR with V3-16S rDNA and pufM gene primers, and the amplifications were then analyzed by DGGE. The DGGE patterns demonstrated the dynamics of community structure and the shift of microbial diversity, which correspond...     

复合吸附材料TLA的制备及其砷氟共除性能的研究

以硫酸钛、硝酸镧和活性炭为原料,制备了新型的TLA复合吸附剂.比较了TLA和活性氧化铝除砷除氟吸附等温线、吸附动力学和pH对除砷除氟效果的影响;通过X射线衍射仪(XRD)和扫描电镜(SEM)对吸附剂进行了表征,并对吸附机理进行了探讨.结果表明,TLA对砷氟的吸附容量显著优于活性氧化铝.在pH为7,砷氟单独存在时,TLA对砷和氟的Langmuir吸附容量分别是30.3mg.g-1和27.8mg.g-1;当砷氟共存时,TLA对砷和氟的Langmuir吸附容量分别是25.1mg.g-1和17.0mg.g-1.TLA对砷、氟的吸附符合拟二级动力学方程.溶液pH值显著影响砷、氟去除效果.电荷分布多位络合模型(Charge-distribution multisite complexation model,CDMUSIC)能准确模拟砷、氟的吸附行为.     

三种氧化铁吸附水环境中砷的试验研究

采用两种人工合成的氧化铁(针铁矿、水铁矿)和赤铁矿作为吸附剂,对含砷(三价砷及三价五价砷混合液)水进行了吸附试验。结果表明,在初始浓度为1200μg/L的As(Ⅲ)溶液中,水铁矿的吸附效果最好,针铁矿和赤铁矿吸附效果较差;在初始pH为7,As(Ⅲ)和As(Ⅴ)摩尔比为1:1的混合液中时,三种铁矿对总砷的吸附效果均随着As/Fe摩尔比的增大而减小;在A(sⅢ)和As(Ⅴ)摩尔比为1:1的混合液中,吸附总砷效果最好的是针铁矿,水铁矿次之,赤铁矿的吸附效果最差;A(sⅤ)的存在对除砷效果有一定的影响,三价砷和五价砷共存时,三种铁矿对其吸附具有一定的选择性。     

Pollutant loads of surface runo inWuhan City Zoo, an urban tourist area

The pollutant loads of surface runoff in an urban tourist area have been investigated for two years in the Wuhan City Zoo, China. Eight sampling sites, including two woodlands, three animal yards, two roofs and one road, were selected for sampling and study. The results indicate that pollutants ranked in a predictable order of decreasing load （e.g. animal yard〉roof〉woodland〉road）, with animal yards acting as the key pollution source in the zoo. Pollutants were transported mainly by particulate form in runoff. Particulate nitrogen and particulate phosphorous accounted on average for 61%, 78% of total pollutant, respectively, over 13 monitored rainfall events. These results indicate the treatment practices should be implemented to improve particulate nutrient removal. Analysis of the M（V） curve indicate that no first flush effect existed in the surface runoff from pervious areas （e.g. woodland, animal ground yard）, whereas a first flush effect was evident in runoff from impervious surfaces （e.g. animal cement yard, roof, road）.     

Tissue distribution of antimony (Sb) in piglets orally given graded levels of Sb (V)

The potential risks from oral intake of soil antimony (Sb) depends mainly on the amount of metal ingested and its bioavailability. Relative bioavailability may be determined by comparing Sb present in soil to a reference compound, taking into account accumulation in different target tissues or excretion. However, due to the lack of scientific knowledge concerning the fate of Sb in the organism, there is a need to study the absorption and distribution of Sb in order to select target tissues for assessment of bioavailability of Sb in soils. Thus, 45 piglets were exposed to a soluble pentavalent antimony salt (KSb(OH)₆), for 15 days at concentrations ranging from 0–1600 µg Sb/kg body weight (BW) per day. Following the exposure period, blood, plasma, liver, spleen, kidneys, hair, bone, bile and urine were obtained to measure Sb concentrations by ICP-MS. Results showed that tissue Sb levels were dose-related. Higher Sb concentrations were found in urine, kidneys, hair, bone and liver. Sb(V) was not detectable in blood and plasma. In the case of highly contaminated soil with soluble forms of Sb in concentrations ranging from 200–1600 µg Sb/kg BW, kidneys, liver and spleen are the most reliable compartments to determine Sb bioavailability from soil. However, for the soils with lower levels of contamination and a low Sb bioaccessibility, urine may serve as a relevant compartment.     

助剂Ga对V2O5-MoO3/TiO2催化剂脱硝性能的影响

对V₂O₅-MoO₃/TiO₂脱硝催化剂进行Ga改性处理,制备了一系列不同Ga₂O₃质量分数的V₂O₅-MoO₃-Ga₂O₃/TiO₂脱硝催化剂。采用XRD、N₂-吸附脱附、H₂-TPR、UV-vis、拉曼光谱、NH₃-TPD等手段对催化剂进行表征。结果显示：Ga的添加对催化剂上MoO_x物种的影响不大,但降低了催化剂上VO_x物种的聚合度,从而提升催化剂的还原性能,同时Ga的添加还减少了催化剂的酸性位。当Ga₂O₃质量分数为0.2%时,V₂O₅-MoO₃-Ga₂O₃/TiO₂催化剂的脱硝性能最佳。     

苦草光合作用日变化对水体环境因子及磷质量浓度的影响

在静态实验系统中通过水下饱和脉冲荧光仪（Diving-PAM）和多参数水质监测仪（YSI）监测沉水植物苦草（Vallisneria natans）叶绿素荧光参数与水质物理指标的日变化,并同时跟踪测定水体中各形态磷的质量浓度,以研究苦草光合作用日变化对水体物理因子和磷质量浓度的影响。结果表明,苦草叶片光合作用的相对电子传递速率（rETR）,非光化学淬灭系数（qN）及快速光响应曲线的变化趋势和叶片表明的光照强度日变化同步,呈单峰曲线变化;光系统Ⅱ（PSⅡ）实际量子产量（Yield）和光化学淬灭系数（qP）与叶片表明的光照强度日变化相反,呈单槽型曲线变化。水体中溶解氧（DO）、pH和氧化还原电位（Eh）的日变化趋势和与苦草光合作用趋势一致,也呈单峰曲线,均在12：00—13：00时达到最高值。水体总磷（TP）与溶解性总磷（DTP）质量浓度在14：00达到最低值（TP 0.015 mg.L-1,DTP 0.010 mg.L-1）,在24：00达到最大值（TP 0.031 mg.L-1,DTP 0.025 mg.L-1）,溶解性活性磷（SRP）质量浓度在6：00—18：00保持在较低的水平,且无明显波动（0.38~2.46μg.L-1）,在24：00达到最大值（9.62μg.L-1）。水体各形态磷的质量浓度变化呈白天降低、夜间升高趋势,水体中各形态磷的质量浓度变化与苦草光合作用日变化趋势相反。实验结果表明,苦草光合作用引起的水体中环境因子的日变化影响了沉积物磷释放的动态平衡过程,从而引起水体磷质量浓度的日变化。