Oxidation of polycyclic aromatic hydrocarbons by horseradish peroxidase in water containing an organic cosolvent

Polycyclic aromatic hydrocarbons (PAHs) are environmental contaminants that are toxic, mutagenic, and carcinogenic. We investigated the horseradish peroxidase (HRP)-catalyzed oxidation of PAHs in water containing N,N-dimethylformamide. Four PAHs (anthracene, phenanthrene, pyrene, and fluoranthene) were investigated using single-PAH and mixed-PAH systems. The results provide useful information regarding the preferential oxidation of anthracene over other PAHs regardless of the reaction time, enzyme dosage, and hydrogen peroxide concentration. The removal of PAHs was found to be very strongly correlated with the ionization potential (IP), and much greater PAH oxidation was observed at a lower IP. The oxidation of anthracene was specifically pH- and temperature-dependent, with the optimal pH and temperature being 8.0 and 40 °C, respectively. The redox mediators 1-hydroxybenzotriazole and veratryl alcohol promoted the transformation of anthracene by HRP; 9,10-anthraquinone was the main product detected from the anthracene oxidation system. The results of this study not only provide a better understanding of the oxidation of PAHs by utilizing a plant biocatalyst, but also provide a theoretical basis for establishing the HRP-catalyzed treatment of PAH-contaminated wastewater.     

Effect of organic amendments on the mobility of trace elements in phytoremediated techno-soils: role of the humic substances

The efficiency of aided phytostabilization using organic amendments such as ramial chipped wood (RCW) and composted sewage sludge (CSS) was studied on contaminated techno-soils, on nine experimental plots. The objective was to characterize the role of fulvic (FA) and humic acids (HA) on the mobilization of trace elements, specifically As, Cu, Mo, Pb and Zn. Results showed that the addition of CSS increased the total organic carbon and nitrogen content more than with RCW and as a result, the C/N ratio in the CSS soil was higher than in the RCW and non-amended (NE) soil, reflecting the high decomposition of soil organic matter in the CSS soil compared with the other soils. The RCW and CSS amendments increased the hydrogen index (HI) values and the oxygen index (OI) values compared with the NE soil, especially for the soil treated with CSS which contained more aliphatic than aromatic compounds. The addition of CSS to the techno-soil significantly increased the percentage of C _org associated with the HA fractions compared with the RCW and NE soils. The soil amended with CSS showed the highest E ₄/E ₆ ratio and the lowest E ₂/E ₃ ratio of FA. Zn and As were more abundant in the FA fraction than in the HA fraction, whereas Pb, Cu and Mo were more associated to HA than to FA in the treated and untreated soils, which may explain the difference in their mobility and availability.     

Degradation of aqueous Rhodamine B by plasma generated along the water surface and its enhancement using nanocrystalline Fe-, Mn-, and Ce-doped TiO2 films

The degradation of aqueous Rhodamine B (RhB) was examined using a dual-channel spark switch module designed to regulate the steepness of pulsed high voltage with microsecond rise time. Depending on the energy per pulse, a spark along the water surface (SPWS) or streamer along the water surface (STWS) was formed. STWS was found to have a better degradation effect and energy efficiency toward RhB than SPWS at the same power; however, addition of H₂O₂ amounts resulted in increased degradation, the effect being more pronounced using SPWS. The initial concentration of RhB also appeared to influence the rate constant of the degradation reaction. Furthermore, TiO₂ films doped with Fe, Mn, and Ce were found to enhance the degradation performance of plasma. A possible reaction mechanism of plasma formation along the water surface was concluded by determination of the main inorganic products in the liquid and gas phases.     

含氨氮催化剂生产废水的处理

采用加入淀粉的短程硝化-反硝化一体化技术处理低碳含NH3-N催化剂废水。通过中试确定了适宜的工艺参数,并在工业化装置上进行了验证。试验结果表明：在DO为0.5 mg/L左右、淀粉加入量为0.25 kg/ m3、HRT=30 h的条件下,短程硝化-反硝化一体化技术具有较好的处理效果,NH3-N去除率大于97%,且具有较强的抗冲击负荷的能力; 出水的COD<100 mg/L,ρ（NH3-N）<10 mg/L,达到GB 8978—1996《污水综合排放标准》的一级排放标准。工业化装置的运行费用以NH3-N计为2.3 元/kg、以废水计为4.6 元/t。该法适用于中低浓度（ρ（NH3-N）<300 mg/L）废水的处理。     

燃煤烟气低温SCR脱硝中试研究

低温选择性催化还原(SCR)脱硝是国内外脱硝技术研发的热点,但目前主要集中在实验室小试范围,无法完全反映催化剂在实际烟气中的运行状况。在30 t/h循环流化床燃煤锅炉脱硫除尘装置后建设了2 000~5 000 m3/h的SCR脱硝中试装置,经系统研究发现,中试使用的蜂窝式催化剂对SO2和NO具有很强的吸附能力,且反应温度、喷氨速率和气体空速均会影响催化脱硝效率。为期5 d的连续运行实验结果表明,催化剂的脱硝效率一直稳定在30%~50%,并未发现明显的失活,这证明设计除雾除尘器、较大的混合器、混合器与反应器间较长的管路均有利于缓解催化剂因SO2、H2O和飞灰中的碱性金属导致的失活。     

微磁场条件下pH冲击对微氧活性污泥表面性质的影响

研究了微磁场条件下pH冲击对处理低负荷葡萄糖废水的微氧活性污泥表面性质的影响。在pH=6.0和9.0的条件下对添加磁粉和无磁粉反应器微氧活性污泥进行15 d的冲击,而后调整pH=7.5进行5 d的恢复实验。对pH冲击下污泥絮凝能力FA、疏水性RH和表面电荷SC的变化情况进行考察,结果表明,有磁粉反应器的各项指标均优于无磁粉反应器。经过5 d的恢复实验,添加磁粉反应器污泥的各指标均能恢复到接近初始值,而无磁粉反应器污泥难以恢复到接近初始值。     

镍基催化剂对污泥微波热解制生物气效能的影响

为实现污水污泥减量化、无害化及资源化的目标,在微波热解污水污泥基础上,进行了镍基催化剂对制取生物气效能影响的研究。采用元素分析对污泥元素进行检测,气/质联用分析(GC-MS)和气相色谱(GC)对热解生物气的组成和含量进行测定。实验结果表明,镍基催化剂的添加对微波热解污水污泥制取生物气有较大促进作用。5%添加量与800℃热解终温条件下具有最佳催化效果:生物气中H2、CO产量最大,H2产量由29 g/kg增加到35.8 g/kg,提升23.4%,CO产量由302.7 g/kg增加到383.3 g/kg,提升26.6%;同时催化剂还能提高热能利用效率,降低热解终温,即5%添加量在700℃热解终温时可达到空白800℃时的产气效果;镍基催化剂主要在500~600℃时发挥催化作用,加快了H2和CO的释放。微波热解污泥制取的生物气具有产量大、富含H2与CO等优点,可推动污水污泥的资源化进程。     

接种微生物与人粪便同步连续投加对好氧堆肥效果的影响简

利用新型梨形筒式好氧堆肥反应器,在通风量为3.0 L/min,搅拌频率为5 min/h的条件下,就不接种微生物、接种土著菌种、枯草芽孢杆菌与酵母菌时人粪便连续投加好氧堆肥效果进行了对比。堆制20 d即2个运行周期中各堆体的温度、含水率、COD、总氮、pH值与GI等的变化表明,接种微生物可以显著提高堆体的升温速率与堆体平均温度、COD降解率、GI（P<0.01）,堆肥可迅速达到完全腐熟。接种土著菌种效果最为明显（P<0.01）,其后相继为枯草芽孢杆菌与酵母菌。接种土著菌种可使堆体温度在50℃以上维持18 d,第8天COD降解率达到61.17%、总氮损失率为25.75%,第6天时GI达到108.22%。     

As(V)在金红石TiO_2颗粒表面吸附特性及机理

通过静态动力学和热力学吸附实验,研究了温度、共存离子以及溶质的初始浓度对As(V)在金红石TiO2颗粒表面吸附的影响,探讨了As(V)在金红石TiO2颗粒表面吸附特性及机理。结果表明,在As(V)初始浓度为10 mg/L,pH为7的条件下,25℃时的吸附量0.41 mg/g高于30℃时的吸附量0.31 mg/g,As(V)在金红石TiO2上的吸附为放热过程。CaCl2和MgCl2的添加对As(V)在金红石TiO2表面吸附起到明显的促进作用。T=25℃,Ca2+或Mg2+浓度为10 mmol/L时,As(V)吸附量分别为0.64和0.56 mg/g,Ca2+比Mg2+对As(V)吸附促进作用强。As(V)在金红石TiO2的吸附等温线符合Frendlich方程,Lagergren二级动力学方程能较好地描述As(V)在金红石TiO2颗粒表面吸附的动力学过程。     

偶氮类染料脱色率的定量构效关系

偶氮类染料的生产和使用过程中存在着三废多、难脱色和污染严重等问题,该染料是印染工业的主要污染物。选取偶氮类染料的分子结构参数和其光催化氧化脱色率之间建立定量结构活性关系(QSAR),进而得到回归方程,为印染废水处理和染料环境行为评价提供理论预测。结果表明,偶氮类染料的光催化氧化脱色率与其结构之间存在着线性相关性,线性方程为:D=0.647μ+66.277,(D为脱色率、μ为偶极矩)R=0.989方程具有预测能力。