好氧条件下生物转鼓同步脱硫脱硝性能及相应动力学模型的优化

为探究高效同步脱硫脱硝的生物工艺,以生物转鼓反应器为实验对象,研究了好氧条件下SO2质量浓度、NOx质量浓度、营养液体积和气体停留时间(EBRT)的变化对生物转鼓同步脱硫脱硝效果的影响,并用动力学模型拟合值与实验数据进行了对比.实验结果表明:生物转鼓同步脱硫脱硝最适条件为SO2质量浓度1200 mg·m-3,NOx质量...     

改性Ti/SnO2-Sb电极催化降解1,4-二氯苯废水试验研究

采用聚合物前驱体法制备了未掺杂、掺杂Cu、掺杂Bi、掺杂Ni的4种Ti/Sn O2-Sb电极,运用SEM和XRD分析电极表面形貌及结构,通过线性极化扫描、循环伏安等测试考察其电化学性能,同时进行1,4二氯苯(p-DCB)降解实验进一步探究电极的电催化氧化特性.SEM和XRD结果表明,掺杂金属可改善电极表面形貌,增大其比表面积;电化学测试表明,Ti/Sn O2-Sb电极的析氧电位并未因金属掺杂而有明显改变,掺杂金属后,Ti/Sn O2-Sb电极具有更优的电催化活性和稳定性.p-DCB降解实验表明,改性Ti/Sn O2-Sb电极对p-DCB的降解效率明显提高,其中Ti/Sn O2-Sb-Cu电极的电催化处理效果最优,电解2 h后p-DCB的去除率即达到87.6%,且p-DCB的降解反应遵循一级反应动力学规律.     

Kinetics of aniline oxidation with chlorine dioxide

For the first time, kinetics of aniline oxidation with chlorine dioxide(ClO2) were investigated systematically by detecting concentration of aniline with HPLC at regular intervals. Results showed that the reaction was first-order both in ClO2 and in aniline, and the oxidation reaction could be described as second-order reaction. Stoichiometric factor η was experimentally determined to be 2.44. The second-order-reaction rate constant k was 0.11L/(mol.s)under condition of pH 6.86 and water temperature(Tw) 287K. Reaction activation energy was 72.31 kJ/mol, indicating that the reaction could take place under usual water treatment conditions. The reaction rate constants in acidic and alkali media were greater than that in neutral medium. Chlorite ion could slightly increase reaction rate in acidic medium. p-aminophenol and azobenzene were detected by GC-MS as intermediates.     

UV-catalytic treatment of spent caustic from ethene plant with hydrogen peroxide and ozone oxidation

The performance of UV/H2O2, UV/O3 and UV/H2O2/O3 oxidation systems for treating spent caustic from an ethylene plant was investigated, in UV/H2O2 system, with the increase of H202 dosage, removal efficiencies of COD and the ratio of biochemical oxygen demand(BOD) to chemical oxygen demand(COD) of the effluent were increased and a better performance was obtained than the H2O2 system alone. In UV/H2O2 system, removal efficiency of COD reach 68% under the optimum condition, and BOD/COD ratio was significantly increased from 0.22 to 0.52. In UV/O3 system, with the increase of O3 dosage, removal efficiency of COD and BOD/COD ratio were increased, and a better performance was obtained than the O3 system alone. Under the optimum condition, removal efficiency of COD was 54%, and BOD/COD ratio was significantly increased from 0.22 to 0.48. In UV/H2O2/O3 system, COD removal efficiency was found to be 22.0% higher than UV/O3 system.     

Preparation and catalytic properties of ZrO2-Al2O3 composite oxide supported nickel catalysts for methane reforming with carbon dioxide

ZrO2-Al2O3 composite oxides and supported Ni catalysts were prepared, and characterized by N2 adsorption/desorption, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques. The catalytic performance and carbon deposition was also investigated. This mesoporous composite oxide is shown to be a promising catalyst support. An increase in the catalytic activity and stability of methane and carbon dioxide reforming reaction was resulted from the zirconia addition, especially at 5wt% ZrO2 content. The Ni catalyst supported ZrO2-Al2O3 has a strong resistance to sintering and the carbon deposition in a relatively long-term reaction.     

Photodegradation mechanism of two dyes: the influence of adsorption behavior on the novel TiO2 particles

The relationship between adsorption behavior and photocatalytic mechanism of the two dyes was investigated. Adsorption isotherms showed that the adsorption of cationic pink FG was Langmuir type behavior, while the reactive brilliant red k-2G was Freundlich type behavior. The increasing pH favored the adsorption of FG but have little effect on the photodegradation. The increasing pH favored the adsorption and the photodegradation of k-2G. The presence of scavenger of hvb^ and OH. radical potassium iodide inhibited the degradation of k-2G, free radicals scavenger tetranitromethane inhibited the photodegradation of FG. These results indicated that the photodegradation of FG mainly via free radicals in solution, and the photodegradation of k-2G was mainly on the catalysts surface or near the interface of solid and solution by react with hvb^ and surface-bound OH.. The different effect of SO4^2- , HCO3^- on the adsorption and photodegradation of two dyes confirmed these results.     

闽江河口短叶茳芏湿地CH4和N2 O排放对氮输入的短期响应

利用静态箱-气相色谱法,研究了氮输入对闽江河口短叶茳芏湿地CH4和N2O排放通量的短期影响.结果表明,高氮输入在不同采样时间均促进了湿地CH4排放,低氮输入在不同时间则具有不同的变化特征.与对照处理相比,低氮和高氮2种处理分别使湿地CH4排放通量增加了-44.35%～1 057.35%和7.15%～667.37%.外源氮输入在24 h内对湿地N2O排放通量具有明显的正激发效应,最高可增加171.60倍和177.79倍,但在8 d后,氮输入对湿地N2O排放的激发效应减弱甚至消失.氮输入在短时间内对湿地土壤Ec、pH和Eh均未产生显著影响.湿地CH4排放通量在对照处理下仅与5 cm Eh存在显著负相关,在低氮处理下仅与10 cm地温呈显著负相关,在高氮处理下则与5 cm Ec、0、5 cm pH以及0、5、10 cm土壤Eh均呈显著相关性,而N2O排放通量在不同处理下与湿地气温、地温、盐度、pH和Eh等环境因子均不存在显著相关性.研究表明,探讨氮输入对湿地温室气体排放的影响应考虑其时间变异性.     

^35S标记法研究土壤中SO^2—4的吸附—解吸行为

本文比较了＾３５Ｓ同位素标记法和两种常规化学分析、一种电化学分析法测定环境样品中ＳＯ＾２－４的优劣。用本法和ＢａＣｒＯ４分光光度法研究土壤对ＳＯ＾２－４的吸附－解吸特征，表明两者测定结果接近，且所得规律一致。酸雨研究中，在样品数量多、ＳＯ＾２－４分析任务重且仪器、设备条件具备时，本法为便捷、准确、较理想的ＳＯ＾２－４测定技术。     

新生态MnO2吸附剂对酸性媒介染料废水脱色特性研究

本文主要报道了一种用于染料废水处理的新型材料即新生态MnO2 及其对三种酸性媒介染料染色废水的脱色作用及影响脱色效果的主要因素。研究结果表明 ,新生态MnO2 对酸性媒介染料的吸附能力很强 ,当染料浓度为2 0 0mg/L、pH <2时 ,其对酸性媒介黑T、酸性媒介绿G和酸性媒介黄GG的脱色率分别达 98.2 %、94.5 %和 96 .4%。染料吸附效果受体系pH值、MnO2 投加量、吸附时间及温度等因素的影响 ,其中pH值是最主要的影响因素。新生态MnO2 对酸性媒介黄GG的吸附作用符合Langmuir吸附等温式     

胶结液注入轮数和体积对微生物加固粉土的影响∗

通过微生物诱导碳酸钙沉积可以将松散土颗粒胶结成整体从而达到加固目的。胶结液的注入轮数和每轮使用的胶结液体积会影响加固效果,但目前关于这方面的研究还不充分。以海相粉土为处理对象,通过室内试验来研究胶结液的注入轮数和体积对加固效果的影响。改变胶结液注入轮数的试验结果表明:随着注入轮数的增加,试样中沉积生成的碳酸钙逐渐增多,碳酸钙的分布比较均匀,加固后的无侧限抗压强度逐渐提高;但当胶结液的注入达到一定轮数后,强度的增长幅度逐渐减缓。改变每轮胶结液体积用量的试验结果表明:胶结液体积的增加会带来碳酸钙数量的增加和强度的提高,但当胶结液体积从1.5Vv(孔隙体积)增加至2Vv后,效果改善不明显。从钙离子用量与无侧限抗压强度的关系也表明,每轮注入的胶结液体积应选择1.5Vv。