Photocatalytic remediation of γ-HCH contaminated soil induced by α-Fe2O3 and TiO2

Heterogeneous photocatalytic degradation of γ-HCH on soil surfaces was carried out to evaluate the photocatalytic effectiveness of α-Fe2O3 and TiO2 toward degrading γ-HCH on soil surfaces. After being spiked with γ-HCH, soil samples were loaded with α-Fe2O3 or TiO2 and exposed to UV-light irradiation. Different catalyst loads(0%, 2%, 5%, 7%, and 10% (wt). α-Fe2O3; 0%, 0.5%, 1%, 2% wt. TiO2) were tested for up to 7 d irradiation. The effects of soil thickness, acidity, and humic substances were also investigated. The obtained results indicated that the γ-HCH photodegradation follows the pseudo-first-order kinetics. The addition of α-Fe2O3 or TiO2 accelerates the photodegradation of γ-HCH, while the photodegradation rate decreases when the content of α-Fe2O3 exceeds 7%(wt.). The degradation rate increases with the soil pH value. Humic substances inhibit the photocatalytic degradation of γ-HCH. Pentachlorocyclohexene, tetrachlorocyclohexene, and trichlorobenzene are detected as photodegradation intermediates, which are gradually degraded with the photodegradation evolution.     

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.     

中国工业园区生态化发展决策优化方法研究

工业是当前中国经济绿色转型升级的关键行业,而工业园区作为工业集聚化发展的主要载体,工业园区生态化发展是解决资源环境问题、实现经济可持续发展的有效途径。本文关注工业园区生态化发展的中长期发展战略和具体方案,致力于通过仿真模拟的方法提出工业园区生态化发展的方向和优化路径,实现研究方法的创新。研究以3E系统(经济—环境—能源)为基础,综合分析工业园区经济发展与能源环境之间的耦合关系,并结合动态投入产出模型和系统动力学模型构建生态化发展决策模型,通过最优化动态模拟方法开展趋势预测和路径研究。通过辛集工业园区的实证和案例研究,对其生态化发展路径进行深入研究,验证了研究方法的科学性和可靠性,能够为工业园区生态化发展提供实践指导。本文为工业园区生态化发展规划提供新的研究方法,为制定合理有效的工业园区综合战略和实施路径提供科学依据。     

活性污泥法处理焦化污水监测值的统计特性

用活性污泥法处理焦化污水,将一年内监测的曝气池山水和入水中酚、氰、氨氮、COD等指标建立数据库,并进行时间序列、正态分布性、自相关和线性回归分析.统计分析结果表明,多数指标呈正态分布而周期性特征不明显;经多元线性回归分析,出水COD与入水COD、出水酚之间的关系较为密切.     

Fe3O4@SA/Ce微球的表征及对染料的吸附特性

以天然高分子化合物海藻酸钠(sodium alginate,SA)为骨架,结合磁性Fe₃O₄和稀土铈离子Ce(Ⅲ)通过溶液反应制备出一种新型的磁性海藻酸铈复合微球(Fe₃O₄@SA;Ce).采用X射线衍射(XRD)、孔结构比表面积分析(BET)、扫描电子显微镜(SEM)、红外光谱(FT-IR)及振动样品强磁计(VSM)对Fe₃O₄@SA;Ce的结构进行了表征,并以直接桃红12B(direct red 12B,DR 12B)和直接橙S(direct orange S,DO S)两种染料为吸附对象,探讨了Fe₃O₄@SA;Ce的吸附剂性能、吸附动力学和热力学.结果表明,Fe₃O₄@SA;Ce对室温下自然pH染料溶液中DR 12B和DO S均表现出良好的吸附效果,吸附量分别可达464 mg·g^-1和730 mg·g^-1.在不同温度下(298、313、328 K),Fe₃O₄@SA;Ce对DR 12B和DO S的吸附过程均可用拟二级吸附动力学方程准确描述.通过等温吸附研究,发现Fe₃O₄@SA;Ce对两种染料的等温吸附较好地符合Freundlich模型.各种表征结果表明,SA与Ce(Ⅲ)和Fe₃O₄交联反应后生成的Fe₃O₄@SA;Ce凝胶球表面有大量深浅不一的褶皱沟纹,形貌发生了显著变化.作为一种绿色环保、制备方法简单、可高效吸附的磁性高分子复合吸附剂,Fe₃O₄@SA;Ce对高浓度染料具有很好的吸附效果,期望能够在染料废水处理中得到广泛应用.     

Optimization of the O3/H2O2 process with response surface methodology for pretreatment of mother liquor of gas field wastewater

• Real ML-GFW with high salinity and high organics was degraded by O₃/H₂O₂ process. • Successful optimization of operation conditions was attained using RSM based on CCD. • Single-factor experiments in advance ensured optimal experimental conditions. • The satisfactory removal efficiency of TOC was achieved in spite of high salinity. • The initial pH plays the most significant role in the degradation of ML-GFW. The present study reports the use of the O₃/H₂O₂ process in the pretreatment of the mother liquor of gas field wastewater (ML-GFW), obtained from the multi-effect distillation treatment of the gas field wastewater. The range of optimal operation conditions was obtained by single-factor experiments. Response surface methodology (RSM) based on the central composite design (CCD) was used for the optimization procedure. A regression model with Total organic carbon (TOC) removal efficiency as the response value was established (R² = 0.9865). The three key factors were arranged according to their significance as: pH>H₂O₂ dosage>ozone flow rate. The model predicted that the best operation conditions could be obtained at a pH of 10.9, an ozone flow rate of 0.8 L/min, and H₂O₂ dosage of 6.2 mL. The dosing ratio of ozone was calculated to be 9.84 mg O₃/mg TOC. The maximum removal efficiency predicted was 75.9%, while the measured value was 72.3%. The relative deviation was found to be in an acceptable range. The ozone utilization and free radical quenching experiments showed that the addition of H₂O₂ promoted the decomposition of ozone to produce hydroxyl radicals (·OH). This also improved the ozone utilization efficiency. Gas chromatography-mass spectrometry (GC-MS) analysis showed that most of the organic matters in ML-GFW were degraded, while some residuals needed further treatment. This study provided the data and the necessary technical supports for further research on the treatment of ML-GFW.     

克雷伯氏菌NY1产絮凝剂的阳离子修饰研究

为简化微生物絮凝剂投加步骤,消除由于助凝剂添加而引起的环境二次污染问题,以3-氯-2-羟丙基三甲基氯化铵(CTA)修饰荷负电的微生物絮凝剂(~-54mV),从而获得荷正电的改性絮凝剂.实验结果显示,CTA与NaOH的摩尔比值是影响阳离子修饰效果的主要因素;阳离子修饰的的最佳条件为:10g微生物絮凝剂, 0.015mol CTA,20%含水率,CTA与NaOH的摩尔比为0.95,80℃反应2h后.在最佳条件下所得阳离子化微生物絮凝剂的Zeta电位可达+16mV,其对高岭土的絮凝率也由阳离子化前的60.5%上升至91%.由阳离子化絮凝剂的结构表征可知,阳离子修饰过程并未改变微生物絮凝剂的根本结构,只是在原微生物絮凝剂基础上引入阳离子基团,从而增加了絮凝剂整体分子量;同时,由于阳离子基团的大量引入,絮凝剂的结晶度增加,从而使其溶解度增加.将阳离子化前后微生物絮凝剂应用于去除铜绿微囊藻,当阳离子化后微生物絮凝剂添加量为40mg/L时,其对藻类的去除率超过98%;而未阳离子修饰的微生物絮凝剂对该藻几乎没有去除效果.     

结合遥感影像的矿山开采沉陷专题信息三维表达

煤矿井下开采引发地表沉陷是一种严重影响生命财产和生产安全的工程形变灾害 ,其形变信息有效表达和精准制图可大大减少矿区变形控制的成本,为矿山安全生产、 保护煤柱留设、塌陷地治理、压煤村庄搬迁、破坏等级判定与损害补偿评估等方面提供 更可靠的技术保障。基于矿山地图、实时卫星遥感影像与开采沉陷变形预计结果等数据 ,采用GIS空间分析和三维可视化技术,对淮北朔里矿区地表移动与变形的下沉（W）、 水平移动（U）、水平变形（ε）、倾斜（i）和曲率（K）等形变类型进行了三维的专 题信息与应用表达,其专题信息能更加直观有效地表达与准确清晰描述开采沉陷的地理 位置、影响范围、受损害地物类型、形变方向与变形量大小等。     

埋藏深度对盐岩储气库溶腔变形的影响研究

以典型的单一溶腔盐岩地下储气库为例,采用ANSYS15.0建立了盐岩储气库计算模型,并通过ANSYS-FLAC3转换软 件将所建模型导入岩土通用计算软件FLAC3D中,最后通过FLAC3D模拟了七种不同埋藏深度情况下盐岩储气库溶腔的变形 情况。数值模拟结果为:随着埋藏深度的增加,盐岩储气库位移近似呈直线增加,盐岩储气库应力同样近似线性增加; 溶腔中上部及溶腔直径最大处位移及应力最大,溶腔变形最大。根据模拟结果,推荐类似本文所建的盐岩储气库埋藏深 度应控制在800～1 000 m为宜,才能保证其运行过程中最大位移不高于1.19 m,最大应力不高于80 MPa。尽管通过 FLAC3D模拟的盐岩地下储气库溶腔形状过于单一,与实际盐岩地下储气库具有一定距离,但是不乏代表性,同样能够为 盐岩储气库运营期间的安全稳定性提供有益的借鉴作用。     

Preconcentration of cadmium and copper ions on magnetic core–shell nanoparticles for determination by flame atomic absorption

Magnetic core–shell nanoparticles modified by (3-aminopropyl) trimethoxy silane were prepared and used as adsorbent for the extraction and preconcentration of cadmium and copper ions. The ions were desorbed with nitric acid followed by determination with flame atomic absorption spectrometry. The extraction conditions were investigated systematically. The method was applied for the determination of Cd(II) and Cu(II) ions in different water samples. The accuracy was also evaluated through analysis of certified reference material.