城市地表灰尘颗粒体积分形特征及其吸附性

以地表灰尘颗粒分析数据为基础,运用分形模型,分析了芜湖市高新技术开发区地表灰尘颗粒的分维数.结果表明:19个地表灰尘样品的粒径较粗,粒径的平均值多出现在140～230 gm之间,峰值多出现在200～400 μm之间;分维数为2.5392～2.7408.平均值为2.665 7,pH值为7.97～12.36,平均值为10.22,呈较强的碱性.分维数与pH值之间的相关系数r=-0.221 0,相关性不明显;地表灰尘分维数对吸附性的影响效果不明显.     

Role of interfacial electron transfer reactions on sulfamethoxazole degradation by reduced nontronite activating H2O2

It has been documented that organic contaminants can be degraded by hydroxyl radicals ( • OH) produced by the activation of H₂ O₂ by Fe(II)-bearing clay. However, the interfacial electron transfer reactions between structural Fe(II) and H 2 O 2 for • OH generation and its effects on contaminant remediation are unclear. In this study, we first investigated the relation between • OH generation sites and sulfamethoxazole (SMX) degradation by activating H₂O₂ using nontronite with different reduction extents. SMX (5.2–16.9 μmol/L) degradation first increased and then decreased with an increase in the reduction extent of nontronite from 22% to 62%, while the • OH production increased continually. Passivization treatment of edge sites and structural variation results revealed that interfacial electron transfer reactions between Fe(II) and H 2 O 2 occur at both the edge and basal plane. The enhancement on basal plane interfacial electron transfer reactions in a high reduction extent rNAu-2 leads to the enhancement on utilization efficiencies of structural Fe(II) and H 2 O 2 for • OH generation.However, the • OH produced at the basal planes is less efficient in oxidizing SMX than that of at edge sites. Oxidation of SMX could be sustainable in the H 2 O 2 /rNAu-2 system through chemically reduction. The results of this study show the importance role of • OH generation sites on antibiotic degradation and provide guidance and potential strategies for antibiotic degradation by Fe(II)-bearing clay minerals in H 2 O 2 -based treatments.     

UV/Fenton法处理酸性红B研究

采用UV/Fenton高级氧化技术对酸性红B模拟废水进行处理,当进水浓度为400mg/L时,确定了各影响因素的最佳投加量:H2O2投加量为2 mL/L,Fe2 投加量为0.08g/L,最佳pH值为4;并采用一级动力学公式对酸性红B降解速率进行拟合,研究了反应条件对速率常数的影响.最后通过对单独UV法、单独Fenton法和UV/Fenton法3种处理方法效果的比较,发现UV与Fenton试剂具有协同作用.     

UV／Fenton法处理酸性红B研究

采用UV／Fenton高级氧化技术对酸性红B模拟废水进行处理，当进水浓度为400mg／L时，确定了各影响因素的最佳投加量：H2O2投加量为2mL／L，Fe^2＋投加量为0．08g／L，最佳pH值为4；并采用一级动力学公式对酸性红B降解速率进行拟合，研究了反应条件对速率常数的影响。最后通过对单独UV法、单独Fenton法和UV／Fenton法3种处理方法效果的比较，发现UV与Fenton试剂具有协同作用。     

太湖不同营养类型湖区沉积物磷的形态与吸附行为的比较

选择太湖不同营养类型的湖区开展了沉积物磷形态与磷吸附行为的研究,结果表明,位于藻型湖区梅梁湾的T1点表层沉积物中的总磷(TP)含量高于位于草型湖区T2点的相应值,且沉积物吸附能(K)值与TP含量显著负相关(ppp0)值随深度递增,大型水生植物的存在促使表层沉积物维持磷汇的功能,T1点沉积物距表层10~15cm处EPC0值最低,故相应疏浚深度宜为10~15cm,这一结果为富营养化湖泊的修复提供了理论依据与技术参数。     

Sorption of simazine to corn straw biochars prepared at different pyrolytic temperatures

Simazine sorption to corn straw biochars prepared at various temperatures (100-600 °C) was examined to understand its sorption behavior as influenced by characteristics of biochars. Biochars were characterized via elemental analysis, BET-N₂ surface area (SA), FTIR and ¹³C NMR. Freundlich and dual-mode models described sorption isotherms well. Positive correlation between log K_oc values and aromatic C contents and negative correlation between log K_oc values and (O + N)/C ratios indicate aromatic-rich biochars have high binding affinity to simazine (charge transfer (π-π*) interactions) and hydrophobic binding may overwhelm H-bonding, respectively. Dual-mode model results suggest adsorption contribution to total sorption increases with carbonization degree. Positive correlation between amounts of adsorption (Q_ad) and SA indicates pore-filling mechanism. Comparison between our results and those obtained with other sorbents indicates corn straw biochars produced at higher temperature can effectively retain simazine. These observations will be helpful for designing biochars as engineered sorbents to remove triazine herbicides.     

Cu2+对有机废物联合发酵产乳酸的影响

利用剩余污泥和厨余垃圾2种有机废物联合发酵,研究了在pH 7.0,温度为35℃,Cu2+投加量分别为0、20、40和100 mg·L-1时,乳酸的含量及其手性的变化规律。同时,探讨联合发酵过程中多糖、蛋白质、氨氮、VFA和pH与乳酸的变化关系。结果表明Cu2+在低浓度时可以促进乳酸的产生：当投加量为20 mg·L-1,发酵第3天总乳酸最高浓度为23.22 g·L-1,较空白提高了77.06%,其中L-及D-乳酸浓度分别达到6.95 g·L-1和16.27 g·L-1。随着Cu2+含量继续提高,总乳酸产量随之下降：在Cu2+100 mg·L-1时,乳酸最高浓度下降至16.55 g·L-1,获得最高值的发酵时间滞后至第6 天。响应面分析表明,发酵体系中D-乳酸的光学纯度随Cu2+投加量整体呈上升趋势。深入研究发现,适量Cu2+在厌氧发酵体系过程中促进了多糖和蛋白质的溶出水解速度,从而提高了酸化的发酵潜力。     

Effects of particle composition and environmental parameters on catalytic hydrodechlorination of trichloroethylene by nanoscale bimetallic Ni-Fe

Catalytic nickel was successfully incorporated into nanoscale iron to enhance its dechlorination efficiency for trichloroethylene （TCE）, one of the most commonly detected chlorinated organic compounds in groundwater. Ethane was the predominant product. The greatest dechlorination efficiency was achieved at 22 molar percent of nickel. This nanoscale Ni-Fe is poorly ordered and inhomogeneous; iron dissolution occurred whereas nickel was relatively stable during the 24-hr reaction. The morphological characterization provided significant new insights on the mechanism of catalytic hydrodcchlorination by bimetallic nanoparticles. TCE degradation and ethane production rates were greatly affected by environmental parameters such as solution pH, temperature and common groundwater ions. Both rate constants decreased and then increased over the pH range of 6.5 to 8.0, with the minimum value occurring at pH 7.5. TCE degradation rate constant showed an increasing trend over the temperature range of 10 to 25℃. However, ethane production rate constant increased and then decreased over the range, with the maximum value occurring at 20℃, Most salts in the solution appeared to enhance the reaction in the first half hour but overall they displayed an inhibitory effect. Combined ions showed a similar effect as individual salts.     

环保型花生种衣剂的研制及防病增产试验

探讨不同助剂对环保型花生种衣剂的作用,研究环保型花生种衣剂的防病增产效果。利用正交试验原理,在环保型花生种衣剂中加入不同浓度组合的助剂,根据花生发芽率和幼苗病虫率筛选出最佳种衣剂配方。同时通过花生种子包衣试验、抑菌试验和大田试验研究改良后的环保型花生种衣剂的防病增产效果。在100 g环保型花生种衣剂中加入1.0 g胺鲜酯、1.5 g紫罗兰色素、0.5 g戊二醇和0.5 g 15%粉锈宁可湿性粉剂后改良效果最佳,在改良后的环保型花生种衣剂作用下的花生发芽率显著增大,幼苗病虫率显著降低,同时抑菌试验和大田试验结果也验证了改良后的效果。该研究结果为环保型花生种衣剂配方的改善提供重要参考。     

高硫煤还原分解磷石膏过程中CaS生成机理研究

在N,2气氛下,利用热重分析仪和管式炉研究了高硫煤还原分解磷石膏过程中CaS的生成机理.研究表明.在1000～1150℃温度范围内.磷石膏中的CaSO4与煤粉或汽化产生的CO反应是生成CaS的主要反应.CaS的生成机理可以通过固-固反应机理、气-固反应机理或联合作用机理等模型进行解释.通过对磷石膏分解产物的XRD-SEM图进行分析,结果表明.不同粒径高硫煤对CaS生成量的影响是通过改变CaS的生成机理来实现的.高硫煤粒径较小时.利于气-固反应的发生,而产生大量CaS,反之则以固-固反应机制为主.CaS的生成也相对难些.