Effects of SO2 and H2O on low-temperature NO conversion over F-V2O5-WO3/TiO2 catalysts

F-V_2 O_5-WO3/Ti02 catalysts were prepared by the impregnation method.As the content of F ions increased from 0.00 to 0.35 wt.%,the NO conversion of F-V_2 O_5-WO_3/TiO_2 catalysts initially increased and then decreased.The 0.2 F-V_2 O_5-WO_3/TiO_2 catalyst(0.2 wt.% F ion)exhibited the best denitration(De-NOx) performance,with more than 95% NO conversion in the temperature range 160-360℃,and 99.0% N2 selectivity between 110 and 280℃.The addition of an appropriate amount of F ions eroded the surface morphology of the catalyst and reduced its grain size,thus enhancing the NO conversion at low temperature as well as the sulfur and water resistance of the V_2 O_5-WO3/Ti02 catalyst.After selective catalytic reduction(SCR) reaction in a gas flow containing SO_2 and H_2 O,the number of NH3 adsorption sites,active component content,specific surface area and pore volume decreased to different degrees.Ammonium sulfate species deposited on the catalyst surface,which blocked part of the active sites and reduced the NO conversion performance of the catalyst.On-line thermal regeneration could not completely recover the catalyst activity,although it prolonged the cumulative life of the catalyst.In addition,a mechanism for the effects of S02 and H_2 O on catalyst NO conversion was proposed.     

An investigation of changes in water quality throughout the drinking water production/distribution chain using toxicological and fluorescence analyses

Changes in water quality from source water to finished water and tap water at two conventional drinking water treatment plants(DWTPs) were monitored.Beside the routine water quality testing,Caenorhabditis elegans-based toxicity assays and the fluorescence excitation–emission matrices technique were also applied.Both DWTPs supplied drinking water that met government standards.Under current test conditions,both the investigated finished water and tap water samples exhibited stronger lethal,genotoxic and reprotoxic potential than the relative source water sample,and the tap water sample was more lethal but tended to be less genotoxic than the corresponding finished water sample.Meanwhile,the nearly complete removal of tryptophan-like substances and newly generated tyrosine-like substances were observed after the treatment of drinking water,and humic-like substances were identified in the tap water.Based on these findings,toxic pollutants,including genotoxic/reproductive toxicants,are produced in the drinking water treatment and/or distribution processes.Moreover,further studies are needed to clarify the potentially important roles of tyrosine-like and humic-like substances in mediating drinking water toxicity and to identify the potential sources of these contaminants.Additionally,tryptophan-like fluorescence may be adopted as a useful parameter to monitor the treatment performance of DWTPs.Our observations provided insights into the importance of utilizing biotoxicity assays and fluorescence spectroscopy as tools to complement the routine evaluation of drinking water.     

Recent advances in catalytic decomposition of ozone

Ozone (O₃), as a harmful air pollutant, has been of wide concern. Safe, efficient, and economical O₃ removal methods urgently need to be developed. Catalytic decomposition is the most promising method for O₃ removal, especially at room temperature or even subzero temperatures. Great efforts have been made to develop high-efficiency catalysts for O₃ decomposition that can operate at low temperatures, high space velocity and high humidity. First, this review describes the general reaction mechanism of O₃ decomposition on noble metal and transition metal oxide catalysts. Then, progress on the O₃ decomposition performance of various catalysts in the past 30 years is summarized in detail. The main focus is the O₃ decomposition performance of manganese oxides, which are divided into supported manganese oxides and non-supported manganese oxides. Methods to improve the activity, stability, and humidity resistance of manganese oxide catalysts for O₃ decomposition are also summarized. The deactivation mechanisms of manganese oxides under dry and humid conditions are discussed. The O₃ decomposition performance of monolithic catalysts is also summarized from the perspective of industrial applications. Finally, the future development directions and prospects of O₃ catalytic decomposition technology are put forward.     

Effects of calcination temperature on physicochemical property and activity of CuSO4/TiO2 ammonia-selective catalytic reduction catalysts

CuSO_4/TiO_2 catalysts with high catalytic activity and excellent resistant to SO_2 and H_2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH_3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO_4/TiO_2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH_3,temperature-programmed reduction of H_2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO_4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO_4 changed surface reducibility of the catalyst and favored the process of NH_3 oxidation to nitrogen oxides(NO_x).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃) decreased largely.     

UV/H2O2 oxidation of tri(2-chloroethyl) phosphate: Intermediate products, degradation pathway and toxicity evaluation

Tri(2-chloroethyl) phosphate (TCEP) with the initial concentration of 5 mg/L was degraded by UV/H₂O₂ oxidation process. The removal rate of TCEP in the UV/H₂O₂ system was 89.1% with the production of Cl^? and PO₄^3? of 0.23 and 0.64 mg/L. The removal rate of total organic carbon of the reaction was 48.8% and the pH reached 3.3 after the reaction. The oxidative degradation process of TCEP in the UV/H₂O₂ system obeyed the first order kinetic reaction with the apparent rate constant of 0.0025 min^?1 (R²=0.9788). The intermediate products were isolated and identified by gas chromatography-mass spectrometer. The addition reaction of HO? and H₂O and the oxidation reaction with H₂O₂ were found during the degradation pathway of 5 mg/L TCEP in the UV/H₂O₂ system. For the first time, environment risk was estimated via the “ecological structure activity relationships” program and acute and chronic toxicity changes of intermediate products were pointed out. The luminescence inhibition rate of photobacterium was used to evaluate the acute toxicity of intermediate products. The results showed that the toxicity of the intermediate products increased with the increase of reaction time, which may be due to the production of chlorine compounds. Some measures should be introduced to the UV/H₂O₂ system to remove the highly toxic Cl-containing compounds, such as a nanofiltration or reverse osmosis unit.     

污水处理过程专家系统的结构特点与应用研究进展

综述了专家系统在污水处理领域的结构和特点、针对的工艺以及应用现状方面取得的研究成果。重点介绍了专家系统中知识的获取和表示、规则的建立以及与故障树和其他人工智能技术的结合情况,并对专家系统在污水处理工艺选择、运行控制以及故障诊断3个阶段的研究现状进行了细致分析。在此基础上,提出了尚需解决的问题以及进一步研究与发展的方向。     

长江口海域生态环境状况及保护对策

为加快推进长江口海域的生态环境保护和修复工作,结合长江经济带大保护,系统总结分析了近20年长江口环境质量和生态监控区的监测结果.结果表明:①长江口海域生态系统长期处于亚健康状态.②长江径流总量呈现波动变化,年均流量无明显的变化,而长江口海域海水环境状况一直较差.③营养盐污染严重,主要污染物是无机氮和活性磷酸盐;浮游生物和底栖生物群落结构不稳定,存在生境破碎化严重、外来生物入侵、赤潮频发、低氧区等诸多生态问题.为加强长江口海域生态环境的保护与修复,建议:①加强顶层设计,推进落实陆海统筹;②科学规划临港产业布局,加强涉海产业的污染管理;③加强污染物入海排放管控,提升海洋环境保护意识;④保障海洋生态建设资金,强化海洋生态保护与建设.      

基于PCA-SOM的北京市平谷区地下水污染溯源

为了解北京市平谷区地下水污染物来源,以平谷区2010—2018年监测数据为基础,使用PCA(主成分分析法)识别了地下水水质指标因子,使用自组织映射识别了污染物的空间分布.结果表明:通过监测指标间的Pearson检验发现, 平谷区地下水电导率与ρ(Ca2+)(p=0.936)、总碱度与ρ(HCO₃2-)(p=0.981)、ρ(Mg2+)与总硬度(p=0.944)指标之间显著相关.地下水化学类型主要以HCO₃-Ca型为主,其次为HCO₃-Mg型.NH₄+、SO₄2-、Cd、Fe(Ⅱ)、NO₂指标空间分布离散性和差异性较大,存在局部富集现象.通过因子分析法筛选出影响平谷区地下水水质的8个公因子,首要影响因子为溶滤-富集作用(贡献率为22.398%),次要影响因子为农业、养殖业和填埋场等人为活动作用(贡献率为16.533%),雨水下渗作用(贡献率为8.035%)、工业源人为活动(贡献率为7.466%)对地下水也有一定影响.通过比较各指标的SOM(Self-Organizing Map,自组织映射)特征图像和监测井映射特征图像,发现NH₄+受山前地带林业、种植业和平原地带农业、养殖业的双重影响,Na+、Mn受平原地带人为活动的影响;同时,NH₄+、NO₃-、NO₂三者之间及Fe(Ⅱ)与Fe(Ⅲ)之间来源不同,Cd、Al、氰化物三者具有同一来源.研究显示,PCA-SOM(PCA与SOM相结合)可以对地下水化学组分来源进行定性识别与定量分析.      

国土空间规划新时代旅游规划的定位与转型

我国已经迈入以国土空间规划引领“多规合一”的空间治理新时代,对各专项规划的管控约束性更严、技术性和衔接性要求更高。为此,本文重新审视了旅游规划的性质和地位,并基于产业专项性和空间融合性特征,将旅游规划分为战略规划、协调规划、发展规划和开发规划。以旅游发展规划为示例,提出了六大转型:规划理念从无限思维向边界思维、融合理念和空间思维转变,编制思路从甲方意志向市场导向转变,规划内容从大而全向专而精转变,技术路线从概念逻辑向空间逻辑转变,规划方式从封闭向开放转变,规划技术从缺乏技术到技术融合转变以期推动旅游规划衔接和融入新时代国土空间规划体系,进一步引领中国旅游产业的转型升级和高质量发展。     

烟花爆竹燃放对大气污染物及PM2.5组分影响

为了解烟花爆竹燃放对保定市大气污染物和PM_2.5中水溶性离子及有机碳（OC）、元素碳（EC）浓度的影响,对保定市春节期间大气污染物和颗粒物组分的浓度特征进行了分析,并评估了烟花爆竹的贡献.结果表明： 2019年春节期间烟花爆竹集中燃放期PM_2.5、PM₁₀、SO₂、NO₂、CO平均浓度比非集中燃放期分别增加了1.3、1.0、1.1、0.4、0.02倍;保定市春节期间禁燃措施施行后,除夕、初一2d污染物平均浓度、最高浓度和高浓度持续时间均明显下降,集中燃放期烟花爆竹燃放对PM_2.5、PM₁₀和SO₂浓度贡献量从50%左右（2018年、2017年）下降至30%左右（2019年）,其中SO₂贡献量下降幅度超过PM_2.5和PM₁₀;组分分析表明,接待中心站点（主城区）、涿州站点（区县建成区）烟花爆竹燃放期K⁺、Mg²⁺、Cl^-浓度在水溶性离子中的总占比分别为39.3%、51.1%,比非燃放期的占比显著上升;烟花爆竹燃放对PM_2.5中K⁺、Mg²⁺、Cl^-浓度贡献率在50%以上,其中对K⁺贡献占比高达89.0%,涿州站点SO₄^2-、K⁺、Mg²⁺、Cl^-的贡献量分别是接待中心站点的2.2、2.1、1.9、1.8倍,燃放期硫氧化率（SOR）、氮氧化率（NOR）相比于非燃放期均有一定程度的升高;集中燃放期OC、EC浓度较非集中燃放期分别升高了2.5、2.1倍,烟花爆竹燃放对OC影响大于EC.