响应面法优化聚丙烯酸/腐殖酸/累托石吸附剂的制备条件

以累托石、丙烯酸及腐殖酸为原料制备出能同时吸附重金属和多环芳烃的吸附剂聚丙烯酸/腐殖酸/累托石,采用响应面试验设计法优化吸附剂的制备条件。利用Design Expert软件,建立了预测吸附剂对Cd2+、菲吸附量的二次回归模型,对回归模型进行了方差分析,并确定了吸附剂的最佳制备条件。结果表明,二次回归模型能较好地模拟Cd2+、菲的吸附量与影响因子丙烯酸中和度、引发剂量和交联剂量之间的关系。各因子对Cd2+吸附量的影响次序为:交联剂量>引发剂量>丙烯酸中和度;对菲吸附量的影响次序为引发剂量>交联剂量>丙烯酸中和度。吸附剂的最佳制备条件为:累托石、丙烯酸和腐殖酸三者的质量比为65∶30∶5,丙烯酸中和度、引发剂量和交联剂量分别为75.16%、2.57%和0.44%。在此优化条件下制备的吸附剂对Cd2+和菲的吸附量分别为170.19 mg/g和7.36 mg/g。     

不同处理条件对石油污染土壤植物修复的影响

针对石油烃植物修复过程中的主要影响因素,研究了不同植物种类、不同土壤调理剂和菌剂使用等不同条件对土壤中石油烃植物修复效果的影响.结果表明,不同种类的植物修复可使总石油烃的年降解率达到37.8％ ～ 73.98％,其中大豆和碱蓬具有较好的修复效果;3种不同土壤调理剂对石油烃污染土壤修复的效果为商业添加剂＞牛粪＞蛭石;先微生物修复后种植植物的处理要优于单独的微生物修复及微生物、植物修复同步进行的处理.     

Photodegradation of quinestrol in waters and the transformation products by UV irradiation

Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through sewage discharge and waste disposal produced by human excretions. In this study, the photodegradation kinetics of quinestrol in various conditions was investigated by UV and solar irradiation. The affecting factors were studied including concentration of hydrogen peroxide, different water types, and the initial concentrations of quinestrol. Concurrently, the transformation products and presumed pathways of quinestrol in distilled water by UV irradiation were identified and proposed. The results showed that the degradation of quinestrol in both irradiation conditions followed the pseudo-first-order kinetics. More rapid degradation was observed by UV irradiation (k = 0.018 min⁻¹) than solar irradiation (k = 0.004 h⁻¹), and the photodegradation rate of quinestrol depended on the concentration of hydrogen peroxide, the initial concentration of quinestrol and water types. The transformation products of quinestrol in distilled water were identified by gas chromatography/mass spectrometry. When exposed to UV irradiation, quinestrol in aqueous solution was rapidly degraded, giving at least ten photodegradation products. The chemical structures of ten degradation products were identified on the basis of mass spectrum interpretation and literature data.     

Comparison of homologous and heterologous formats in nanocolloidal gold-based immunoassays for parathion residue determination

The effectiveness of homologous and heterologous formats in a nanocolloidal gold-based immunoassay for pesticide residue determination was investigated. Parathion, one of the most toxic organophosphorus pesticides, was used as the target analyte. One-step homologous and heterologous test strips based on a nanocolloidal gold-labeled monoclonal antibody were developed for the rapid detection of parathion residues. The results showed that the heterologous format was more effective than the homologous format, being more sensitive, more specific to parathion and more tolerant of matrix interferences. The best competitive hapten was found to have a moderate heterology and the opposite electronic distribution to the immunizing hapten. The detection limits for parathion using the preferred heterologous strip were 1 μg/L in water samples and 5 μg/kg in soil and food samples.     

Persistence of repeated triadimefon application and its impact on soil microbial functional diversity

The effects of repeated applications of the fungicide triadimefon in agricultural soil on the microbial functional diversity of the soil and on the persistence of the fungicide in the soil were investigated under laboratory conditions. The degradation half-lives of triadimefon at the recommended dosage, simulated by a first-order kinetic model, were 23.90, 22.95, and 21.52 days for the first, second, and third applications, respectively. Throughout this study, no significant inhibition of the Shannon-Wiener index (H') was observed. However, the Simpson index (1/D) and the McIntosh index (U) were obviously reduced (p ≤ 0.05) during the initial 3 days after the first triadimefon application and thereafter, gradually recovered to or exceeded the level of the control soil. A similar trend in variation but with a faster recovery in the 1/D and U was observed after the second and third triadimefon applications, respectively. Taken together, the above results indicate that the repeated application of triadimefon enhanced the degradation rate of the fungicide and the recovery rate of the soil microbial functional diversity. It is concluded that repeated triadimefon applications in soil have a transient or temporary inhibitory effect on soil microbial communities.     

Characteristics of precipitation chemistry at Lushan Mountain, East China: 1992–2009

Introduction

Trends in precipitation pH and conductivity during 1992?C2009, and in ionic compositions from January 2007 to June 2009, are reported from Lushan Mountain, one of the highest mountains in mid-east China. Annual mean pH was in the range of 4.35?C5.01 and showed a statistically very significant (P?P?Results and discussions Over the period of study, Lushan Mountain received more rainfall in spring and summer. The pH values varied seasonally with winter minima. The winter multiyear seasonal mean pH was 4.35. The corresponding summer value was 4.88. SO ₄ ^2? and NO ₃ ^? were the main anions, and NH ₄ ⁺ and Ca²⁺ the main cations. The anion to cation ratio was 0.8?C1.0, and that of [SO ₄ ^2? ] to [NO ₃ ^? ] was 2.4-3.0, much lower than that of the 1980s. However, sulfuric acid was still the main acid present. The ratio of [NH ₄ ⁺ ] to [Ca²⁺] was about 1.0, suggesting that these two alkaline substances provided close acid neutralizing capacity. The ratio of [Cl^?] to [Na⁺] was about 0.67, somewhat lower than that of natural precipitation.

Conclusions

Ionic composition varied seasonally and was closely correlated to the amounts of rainfall and pollution. Trajectory analyses showed that the trajectories to Lushan Mountain could be classified in six clusters and trajectories originating from the South Sea and the areas surrounding Lushan Mountain had the greatest impacts on precipitation chemistry.     

VFAs、TOC及COD作为生物除磷能力指标的探讨

在实际生活污水的处理中,研究了通过A/O运行模式对生物除磷过程中磷的变化情况及在厌氧释磷过程中COD、TOC与VFAs变化之间的关系。结果表明,在厌氧释磷过程中VFAs的变化更能准确地反映系统内释磷进程,实际生活污水中能直接用于磷释放的有机物含量占COD的13.33%,并且释放1 mg P所需VFAs为1.401 mg,此值明显低于前期研究结果。通过对COD、TOC和VFAs 3种组分的分析,可将实际生活污水中的有机底物分为3类:易生物降解含碳有机物、难降解的含碳有机物和水中存在的无机性还原物质,含量分别占COD的13.33%、31.7%和54.97%,其中只有13.33%的含量对生物释磷有直接作用,并可对实际生活污水除磷有指导意义。     

磷酸铵镁沉淀法预处理垃圾渗滤液

探讨了用磷酸铵镁沉淀法预处理垃圾渗滤液时,沉淀剂种类、pH值、物质摩尔配比和反应时间等因素对氨氮去除效果的影响。得出了处理氨氮浓度为2 677.34 mg/L的垃圾渗滤液时,在兼顾所用镁盐量尽量低和处理出水氨氮或磷酸盐的残留量都比较低的较佳实验条件为:沉淀剂种类为:MgSO4.7H2O和Na2HPO4.12H2O,反应时间为20 min,pH=9.5,n(Mg)∶n(P)∶n(N)=1.3∶1.15∶1.0。在较佳实验条件下,垃圾渗滤液的NH3-N去除率为97.05%,处理出水PO34--P含量为8.35 mg/L,NH3-N含量为75.86 mg/L。对所得沉淀物进行了成分分析和X-衍射光谱、扫描电镜表征,表明大部分沉淀物为磷酸铵镁物质。     

响应面法优化超临界水氧化处理农药废水

在间歇式超临界水氧化系统中对草甘膦农药废水进行降解实验。选取温度、反应时间、过氧量3个量为因素量,总有机碳(TOC)去除率为响应量进行中心组合设计（CCD）。在实验的基础上,利用响应面分析法（RSM）对实验结果进行分析及参数优化：建立了TOC去除率与各个因素关系的二次多项式数学模型;分析了各个因素单独的及相互作用对TOC去除率的影响;优化结果表明,在温度483℃、反应时间29.2 min、过氧量148.4%的条件下,达到了最佳效果,此时TOC的去除率为100%。     

改性粉煤灰对糖蜜废水的吸附效果及机理

采用改性粉煤灰(MCFA)吸附糖蜜废水中的有机污染物,对吸附行为和机理进行了考察和分析。结果表明,MCFA投加量为30 g/L及pH为5.0的优化条件下,COD去除率为88.6%,饱和吸附量为89.7 mg COD/g MCFA。准二级方程能更好地描述糖蜜废水在MCFA上的吸附动力学。颗粒内扩散方程结果表明孔扩散并非唯一的速度控制步骤。吸附平衡表明,Freundlich等温线最符合吸附模式,为优惠吸附。D-R模式中的吸附自由能Ea值推断更可能是物理吸附而不是化学吸附。吸附热力学参数ΔG0(<0)、ΔH0(5.130 kJ/mol)和ΔS0(19.936 J/(mol.K))表明MCFA对糖蜜废水的吸附过程为可行的,自发性的吸热反应。