团粒喷播在废弃采石场生态恢复方面的应用

废弃采石场严重影响城市周边的生态景观,极易导致生态环境的继续恶化。以文登某一采石场破损山体的绿化工程为例,运用团粒喷播生态修复技术对废弃矿山进行生态性治理,并探讨其生态恢复方法,以期为今后废弃矿山的残损山体植被恢复和生态环境重建提供参考。     

低温A/O-MBR工艺启动试验研究

研究了A/O-MBR工艺低温(水温在5~12℃)启动效能,结果表明,低温下A/O-MBR工艺启动迅速,活性污泥的培养驯化时间较短。启动过程中根据出水水质情况,逐渐提高负荷,运行34 d,系统对COD的去除率能达到90%以上,系统对氨氮的去除率能达到96%以上,至稳定运行后氨氮的负荷平均可达到0.419kg/(m3.d),反硝化效果系统去除率基本能稳定在60%左右。     

电渗析法再生CO_2电还原电解液的研究

探索了电渗析法再生CO2电还原电解液的可行性。以HCOOK溶液作为CO2电还原反应后的模拟液,采用单室电渗析装置对其进行再生,考察了电流、时间、温度等操作条件对电流效率和再生率的影响,研究结果表明:在常温条件下,操作电流低于极限电流时,采用电渗析法再生CO2电还原电解液具有高的电流效率和再生率。     

电沉积法处理电解锌漂洗废水的动力学研究

采用电沉积法处理电解锌漂洗工艺废水,以回收废水中的重金属资源。在不同实验条件下对电沉积反应过程中电沉积反应速率及其影响因素进行了研究,结果表明,电沉积回收重金属锌符合准一级动力学规律,当V=6 V时,速率常数k=0.0214。最佳实验条件为:槽电压V=6 V、电解时间为45~60 min、pH为2.5~3.5,反应过程中应充分搅拌。利用电沉积法处理电解锌漂洗废水,将重金属Zn2+还原为单质锌,处理废水的同时实现重金属资源的回收,在工业中有较好的应用前景。     

电石渣和石灰对污泥的改性效果比较

在含水率为86.1%的脱水污泥中分别添加10%的电石渣和工业生石灰,其搅拌30min后及自然晾晒24,48,72,96,120 h后的含水率持续线性下降,自然晾晒120 h后可达到填埋标准;添加电石渣及石灰的污泥,其单位质量水分蒸发速率与原污泥有本质差异;两种改性剂均可使污泥比阻降低50%左右;经板框压滤机压滤出的泥饼...     

CFD技术在水处理紫外消毒中的应用

介绍了紫外消毒在水处理中应用的现状,阐述了计算流体力学(CFD)的基本原理及其应用背景;论述了CFD技术在紫外消毒模型建立方面的关键因素:水力、辐射和剂量模拟;从消毒效率预测和设备结构优化两个方面对CFD技术在水处理紫外消毒中的应用进行了分析,并对其前景进行了展望,提出了今后的研究重点。     

四川某中小城镇污水处理厂进水水质统计分析

生活污水水质对处理工艺的选择、设计参数的选取以及稳定运行十分重要。运用SPSS软件,对四川某中小城镇污水处理厂为期一年的进水指标(水量、COD、氨氮、总磷、pH、SS)进行方差和相关性分析。方差分析结果显示进水量、氨氮和SS在月份和季节之间存在显著性差异,而总磷和pH仅在月份之间存在显著差异,COD在季度和月份之间无显著性差异;指标相关性分析表明,进水量和氨氮之间呈负相关,氨氮和总磷、COD和总磷之间呈正相关,且相关性显著。在此分析的基础上对污水处理厂设计、工艺选择及运行管理提出了一些建议。     

Effect of platinum on the photocatalytic degradation of chlorinated organic compound

TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2, H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of e ciently decomposing gaseous DCM in air.     

Removal of copper ions from aqueous solution by calcium alginate immobilized kaolin

Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin (kaolin/CA), was prepared using a sol-gel method. The e ects of contact time, pH, adsorbent dose, and temperature on Cu2+ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.     

Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous silicates hybrid materials

Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water. A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment.