选择性去除香烟烟气中亚硝胺的研究

沸石具有选择性吸附和催化去除亚硝胺的功能.使用沸石添加剂和/或微波辐射预处理,可将香烟侧流烟气中致癌性物质亚硝胺的含量降低约50%,主流烟气中降低60-90%,能有效地减轻吸烟对于环境的污染.     

生物膜与A/O工艺耦合快速降解氨氮

应用由城市污水处理厂序批式间歇反应器(SBR)中筛选得到的4株特殊氨氧化菌,分别在SBR和有回流的生物膜与A/O工艺耦合体系培养中,考察其降解低碳高氨氮废水的功能.结果表明,自养硝化与异养氨氧化菌的混合菌群较单一自养硝化菌株降解氨氮速率快;在生物膜与A/O工艺耦合系统中,自养硝化与异养氨氧化菌协同代谢加速氨氮氧化脱除,氨氮脱除速率远比SBR系统快.对生物膜与A/O工艺耦合系统中氨氮脱除动力学进行了研究,模拟了NH4 、NO2-质量浓度与氨氮脱除比速率之间的关系,模型得到了较好的验证.     

生物酶催化技术在垃圾渗滤液处理中的应用

针对垃圾渗滤液的特性及目前处理工艺普遍无法达标的问题,提出应用生物酶催化技术处理垃圾渗滤液的方法,可以高效迅速降解污染物,提高污染物去除效率,减少投资及处理费用,为垃圾渗滤液处理的技术升级与工艺探索提供新思路。     

Comparison of Catalytic Degradation of Aniline by Immobilized Iron Oxide Catalysts

Abstract In this study, iron oxides immobilized onto silica and alumina granular carriers in a fluidized-bed reactor were applied as silica granule (SG) and alumina granule (AG) catalysts, respectively; the SG and AG catalysts were used to explore the catalytic decomposition of H2O2. Effects of H2O2 concentration and temperature on the oxidation of aniline were determined to compare the reactive efficiencies of the SG and AG catalysts. Results showed that H2O2 decomposition could be efficiently catalyzed by the SG and AG catalysts. Degradation rates of aniline increased with increasing H2O2 concentration and temperature in both catalyst systems. The AG catalyst (smaller particle size) had more surface sites for precipitation of iron oxide than the SG catalyst (larger particle size). Consequently, in the initial stages of the reaction, hydroxyl radicals (?OH) were generated more rapidly with the AG catalyst than with the SG catalyst and the degradation of aniline by the AG catalyst was faster than that by ...     

活性炭催化臭氧氧化处理染料废水生化出水研究

采用饱和活性炭作为臭氧氧化催化剂,对染料废水生化出水进行深度处理.以废水COD、DOC去除率为指标,考察饱和活性炭对臭氧的催化效果.使用6种不同的活性炭作为催化剂(编号1^#~6^#),并将6^#活性炭采用KMnO₄、NaOH、ZnCl₂、H₂SO₄、H₃PO₄进行表面处理,在活性炭的孔体积、酸碱基团等表面性质测定的基础上,探讨活性炭性质与催化臭氧化效率的关系.结果显示,活性炭催化效果与大孔体积密切相关;另一方面,使用微孔膜片减小臭氧气泡尺寸,增大臭氧的传质面积,提高臭氧利用率,可以改善臭氧/活性炭催化氧化处理效果.     

Fe3O4/FeS2活化H2O2降解典型苯胂酸类污染物

利用水热法成功制备了Fe₃O₄/FeS₂催化剂,并将其用于构建非均相芬顿体系降解典型的苯胂酸类污染物（洛克沙胂,ROX）.XRD、SEM、XPS和磁学测量系统（VSM）等表征结果表明,Fe₃O₄/FeS₂呈明显的颗粒状且具有良好的磁性.降解实验结果显示,在最优条件下（初始pH值为4.5、ROX起始浓度为20mg/L、Fe₃O₄/FeS₂投加量为0.15g/L和H₂O₂浓度为0.034g/L,Fe₃O₄/FeS₂介导的非均相芬顿体系可以超快速降解ROX,1min后的降解效率达到96.74%,明显优于单独的Fe₃O₄或FeS₂体系.此外,Fe₃O₄/FeS₂可以通过磁铁进行快速回收利用,同时也具有良好的重复利用性能,使用3次后,ROX的降解效率仍超过80%.机理分析表明,Fe₃O₄/FeS₂能够快速地催化H₂O₂产生具有强氧化性的羟基自由基（·OH）.在·OH的作-用下,ROX分子结构中C-As、C-N和C-C等化学键发生断裂,发生脱砷、脱硝和开环等反应,进而生成一系列的有机产物（如酚类、醌类、小分子有机酸等）和无机产物（As （V）和NO₃^-）.之后,无机砷能够被吸附在催化剂表面,而有机产物则进一步被矿化.     

Enhanced activation of peroxydisulfate by strontium modified BiFeO3perovskite for ciprofloxacin degradation

A series of Sr-doped BiFeO₃ perovskites (Bi_1-xSr_xFeO₃, BSFO) fabricated via sol-gel method was applied as peroxydisulfate (PDS) activator for ciprofloxacin (CIP) degradation. Various technologies were used to characterize the morphology and physicochemical features of prepared BSFO samples and the results indicated that Sr was successfully inserted into the perovskites lattice. The catalytic performance of BiFeO₃ was significantly boosted by strontium doping. Specifically, Bi_0.9Sr_0.1FeO₃ (0.1BSFO) exhibited the highest catalytic performance for PDS activation to remove CIP, where 95% of CIP (10 mg/L) could be degraded with the addition of 1 g/L 0.1BSFO and 1 mmol/L PDS within 60 min. Moreover, 0.1BSFO displayed high reusability and stability with lower metal leaching. Weak acidic condition was preferred to neutral and alkaline conditions in 0.1BSFO/PDS system. The boosted catalytic performance can be interpreted as the lower oxidation state of Fe and the existence of affluent oxygen vacancies generated by Sr doping, that induced the formation of singlet oxygen (¹O₂) which was confirmed as the dominant reactive species by radical scavenging studies and electron spin resonance (ESR) tests. The catalytic oxidation mechanism related to major ¹O₂ and minor free radicals was proposed. Current study opens a new avenue to develop effective A-site modified perovskite and expands their application for PDS activation in wastewater remediation.     

KCeO_2MnPcX对表面活性剂的催化氧化性能研究

研究了一种新型含稀土酞菁锰(KCeO2MnPcX)催化剂对水中表面活性剂直链烷基苯磺酸钠氧化降解的催化性能,讨论了影响催化氧化反应的各种因素,并确定了最佳反应条件。同时初步探讨了这种催化剂对表面活性剂的催化氧化机理,为处理表面活性剂废水提供了新的途径。     

Carbon‐neutral jet‐fuel re‐synthesised from sequestrated CO2

A chemical pathway combining reverse water gas shift, Fischer‐Tropsch synthesis and hydro‐cracking was considered to re‐synthesise jet fuel from CO₂ captured at high purity by oxy‐fuelling of a typical coal‐fired power station (Drax, UK). The oxygen for oxy‐fuelling and hydrogen for the fuel re‐synthesis process are sourced by electrolysis of water. According to material and energy balances , 3.1 MT/year of jet fuel and 1.6 MT/year each of gas oil and naphtha can be produced from the Drax annual emissions of 20 MT of CO₂, sufficient to supply 23% of the UK jet fuel requirements. The overall re‐synthesis requires 16.9 GW, to be sourced renewably from (offshore) wind power, and releases 4.4 GW of exothermic energy giving scope for improvements via process integration. The energy re‐synthesis penalty was 82% ideally and 95% on a practical basis. With the cost of offshore wind power predicted to reduce to 2.0 p/kWh by 2020, this ‘re‐syn’ jet fuel would be competitive with conventional jet fuel, especially if carbon taxes apply. The re‐use of CO₂ sequestrated from coal power stations to form jet‐fuel would halve the combined CO₂ emissions from the coal power and aviation sectors.     

Removing lignin model pollutants with BiFeO3–g-C3N4 compound as an efficient visible-light-heterogeneous Fenton-like catalyst

BiFeO_3–g-C_3N_4 nanoscaled composite was prepared with a hydrothermal method and evaluated as a highly efficient photo-Fenton like catalyst under visible light irradiation. The BiFeO_3–g-C_3N_4 composite exhibited much stronger adsorption ability to lignin model pollutant(guaiacol) than that of BiFeO_3, which may be due to the higher specific surface area(BiFeO_3–g-C_3N_4: 35.59 m~2/g BiFeO_3: 7.42 m~2/g) and the adsorption form of π–π stack between g-C_3N_4 and guaiacol. The composite exhibited excellent visible light-Fenton like catalysis activity, being influenced by the solution pH value and the proportions of BiFeO_3 and g-C_3N_4 nanosheets. Under optimal conditions with visible light irradiation, the BiFeO_3–g-C_3N_4 composite yielded fast degradation of guaiacol with an apparent rate constant of 0.0452 min~(-1), which were 5.21 and 6.80 folds of that achieved by using BiFeO_3 and the mixture of BiFeO_3 and g-C_3N_4 nanosheets, respectively. The significantly enhanced visible light-Fenton like catalytic properties of the BiFeO_3–g-C_3N_4 composite in comparison with that of BiFeO_3 was attributed to a large surface area, much increased adsorption capacity and the semiconductor coupling effect between BiFeO_3 and g-C_3N_4 in the composite.