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.     

基于地形位置指数的赤水河流域植被时空变化研究

地形因子和植被覆盖是区域灾害评价的关键指标,也是山区型村镇建设生态安全评估的重要内容.为探析山区型村镇建设的生态约束条件,以赤水河流域为研究对象,基于1998—2018年SPOT_VGT NDVI数据,利用地形位置指数（Topographic Position Index,TPI）和坡度位置指数方法,研究了赤水河流域植被生长季NDVI时空变化及地形分异特征.结果表明:①赤水河流域内,1998—2018年植被生长季平均NDVI呈缓慢上升趋势,斜率为0.004 7;NDVI>0.60的集中连片区域主要分布在古蔺县北部、赤水市大部和习水县西北部,占赤水河流域总面积的8.42%;Sen's slope在0.009~0.015区间时,赤水河流域植被生长增强趋势最明显,主要集中分布在赤水河中上游、二道河以及下游的大同河干流地区.②TPI在-39.4~34.3区间的面积最多,为6 221.63 km2,占赤水河流域总面积的34.05%;将赤水河流域坡度类型划分为山脊、上坡、中坡、平坡、下坡、山谷6个坡度位置类型,其中,中坡面积（7 792.02 km2）最大,占流域总面积的42.64%,表明TPI数值较小且坡度大于5°的区域是赤水河流域地形主体.③赤水河流域植被在山脊的平均NDVI最高,为0.747,且山脊平均Sen's slope最高,为0.007 2;山谷平均NDVI最低,为0.709.研究显示,赤水河流域植被分布在118.5~486.9的TPI区间或分布在山脊处时整体生长较好,且生长增强趋势最明显.      

辽东湾近岸海域沉积物石油类分布特征及污染状况

利用2015年－2017年海洋环境监测数据,对辽东湾近岸海域沉积物石油类含量时空分布状况进行阐述,对其污染状况进行分析,对其污染来源进行讨论。研究结果表明,2015年－2017年辽东湾近岸海域沉积物石油类含量范围为1.5×10?6~2790.0×10?6,中位值为62.7×10?6。2015年－2017年辽东湾海洋功能区内沉积物石油类含量的总中位值大小顺序（前三位）为港口航运区>保留区>农渔业区。2015年－2017年辽东湾海洋功能区内沉积物石油类站位总超标率大小顺序（前四位）为工业与城镇用海区>保留区>农渔业区>港口航运区。石油类主要产生于港口航运区、工业与城镇用海区沿岸、保留区沿岸、农渔业区等生产活动较为频繁的区域。     

Well-to-wheels greenhouse gas and air pollutant emissions from battery electric vehicles in China

Mitigation and Adaptation Strategies for Global Change - Electric vehicles (EVs) play a crucial role in addressing climate change and urban air quality concerns. China has emerged as the global...     

基层卫生医疗机构财务管理战略对环境污染的影响分析研究

基层卫生医疗机构财务的优化管理能降低环境污染,定量分析基层卫生医疗机构财务管理战略对环境污染的影响,优化基层医疗机构的财务管理水平,从而抑制环境污染,提出基于关联规则统计分析模型的基层卫生医疗机构财务管理模型。结合定量回归分析方法进行环境污染的影响因素分析,采用解释变量的相关性分析方法进行统计平均检验,构建检测统计量和判决统计量进行环境污染影响及医疗卫生结构财务管理的关联规则分析评估,提高基层医疗结构财务管理的智能化水平。     

分光光度法测定染色废水的色度

为消除测定染色废水色度的主观误差，采用分光光度法测定染色废水的色度，与稀释倍数法相比，具有精确，重现性好，适用范围广等特点，ＰＨ值对色度的测定有明显影响，控制ＰＨ值为７．６０，测定色度具有可比性。