O3/·OH簇射烟气脱除甲苯的数值模拟

利用Fluent软件耦合化学反应机理对O₃与·OH簇射烟气脱除甲苯进行了数值模拟。针对圆形面为入射面的圆柱形管道,通过模拟计算不同位置截面上的甲苯平均浓度,得到管道各个位置的甲苯脱除效率。在不同温度、射流速度、气体组分、自由基配比等工况条件下,模拟研究O₃/·OH对甲苯的脱除规律,分析影响O₃/·OH对甲苯脱除效率的关键因素。结果发现,提升温度对脱除效率有较大提升,而自由基浓度、射流速度、水分浓度与氧气浓度等参数均对脱除甲苯效率均有一定影响。由于在复杂的烟道系统中O₃具有更长的活性周期,因此,比·OH有更高的甲苯脱除效率,约4%的优势。当O₃和·OH混合配比为20%时,脱除效率较其他配比情况要高出约5%,这表明·OH和O₃可协同进行甲苯脱除。本研究可为优化含甲苯的焚烧废气脱除净化技术提供参考。     

钙基半干法燃煤烟气脱硫技术的影响因素

半干法烟气脱硫技术因具有耗水量少、产物易处理等特点而备受关注。基于固定床反应器研究了反应温度、脱硫剂Ca(OH)₂颗粒粒径、反应空速及烟气中水蒸气体积分数对Ca(OH)₂脱硫性能的影响。结果表明,Ca(OH)₂颗粒粒径的减小、反应空速的降低、烟气中水蒸气体积分数的提高及低反应温度等因素,有利于SO₂的脱除、Ca(OH)₂利用率的提高及Ca/S的降低。当Ca(OH)₂颗粒的平均粒径为0.58 mm、反应空速为2 500 h⁻¹、模拟烟气中水蒸气体积分数为12%、反应温度为55 ℃时,可获得最佳脱硫效果。在SO₂穿透浓度35 mg·Nm⁻³下,Ca(OH)₂的利用率可达到71.3%,此时Ca/S为1.4。在上述条件下,SO₂达到穿透浓度时,通过实施脉冲增湿可使穿透时间延长、Ca(OH)₂利用率进一步提升至75.7%。本研究结果可为半干法脱硫工艺的改进提供参考。     

顺磁共振法测定气相中OH自由基的研究

采和电子顺磁共振（ＥＰＲ）法测定气相中ＯＨ自由基的研究表明,４＝ＰＯ敢相中ＯＨ交好自旋捕集剂,得到的４－ＰＯＢＮ－ＯＨ加合物稳定性媸,样品避光保存２ｄ后,测得ＥＰＲ谱的峰形和大小不变,测得ＯＨ加合物的ＥＰＲ谱中超精细偶合常数分别为αＮ＝１．４５ｍＴ和αＨβ＝０．２２ｍＴ,除去样品溶液中微量的Ｏ２,将改善ＥＰＲ谱的峰形。还报字用这种方法对上海地区大气中采样实测得到ＯＨ加合物的ＥＰＲ谱,它与实验室模拟     

蜂窝陶瓷催化臭氧化降解水中草酸的研究

实验比较了单独臭氧氧化、蜂窝陶瓷催化臭氧化和蜂窝陶瓷催化剂吸附3种工艺去除水中草酸的降解效果.结果表明,蜂窝陶瓷催化臭氧化、单独臭氧氧化和蜂窝陶瓷催化剂吸附对水中草酸的去除率分别为37 .6%、2 .2%和0 .4%,蜂窝陶瓷催化剂的存在显著提高了臭氧氧化降解水中草酸的去除效果.添加叔丁醇的浓度为5、10和15 mg·L^-1时,催化臭氧化对草酸的去除率分别降低了24 .1%、29 .0%和30 .1%,证明蜂窝陶瓷催化臭氧化降解水中草酸遵循·OH氧化机理,即非均相的催化剂表面强化了·OH的引发.TOC测试结果显示,蜂窝陶瓷催化臭氧化工艺可以将草酸彻底矿化,无中间产物生成.反应温度与草酸的去除效果成正相关性,当水体温度为10、20、30和40℃时,蜂窝陶瓷催化臭氧化降解水中草酸的去除率分别为16 .4%、37 .6%、61 .3%和68 .2%.     

Rates of production of hydroxyl radicals and singlet oxygen from irradiated compost

The use of organic matter from compost to promote the catalytic photodegradation of micropollutants by solar light appears to be environmentally promising. However, quantitative evaluation of the photodegradation potential of the compost is needed. Our goal was to measure the formation rate of hydroxyl radicals and singlet oxygen, two strongly oxidant species, from irradiated compost organic matter. These two reactive species were photogenerated in all of our extracts regardless of the origin of the compost or the extraction procedure; however, their formation rates increased with composting time. Two herbicides and a fungicide were successfully photodegraded when irradiated with simulated or natural solar light in the presence of the compost organic matter or compost suspensions. For reasons of simplification and ease, the use of the latter is recommended in practice.     

锰铜复合催化剂常温催化氧化NO

采用浸渍法,以γA1₂O₃为载体制备了常温下对NO具有良好催化氧化活性的Mn-Cu复合催化剂。系统考察催化剂组分、焙烧温度等与催化剂性能的关系,结果显示200℃干燥所得催化剂的活性最好,催化剂15%Mn-24%Cu/Al₂O₃在常温下对NO的催化氧化效率达到50%以上。XRD分析表明,催化剂活性组分为Cu（OH）Cl,且随反应时间延长催化性能下降,其物相由Cu（OH）Cl转变为活性较低的Cu₂（OH）₃Cl相。     

Heterogeneous reactions of suspended parathion, malathion, and fenthion particles with NO(3) radicals

Organophosphorus pesticides (OPPs) emit into the atmosphere in both gas and particulate phases via spray drift from treatments and post-application emission, but most of their degradations in the atmosphere are not well known. In this study, the heterogeneous reactions of nitrate (NO₃) radicals with three typical OPPs (parathion, malathion, and fenthion) absorbed on azelaic acid particles are investigated using an online vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). The reaction products observed with the VUV-ATOFMS are identified on the basis of GC/MS analysis of the products in the reaction between NO₃ radicals and the coating of the pesticide. Paraoxon is identified as the only product of parathion; malaoxon and bis(1,2-bis-ethoxycarbonylethyl)disulfide as the products of malathion; fenoxon, fenoxon sulfoxide, fenthion sulfoxide, fenoxon sulfone, and fenthion sulfone as the products of fenthion. The degradation rates of parathion, malathion, and fenthion under the experimental conditions are 5.5 × 10⁻³, 5.6 × 10⁻², and 3.3 × 10⁻² s⁻¹, respectively. The pathways of the heterogeneous reactions between the three OPPs and NO₃ radicals are proposed. The experimental results reveal the possible transformations of these OPPs through the oxidation of NO₃ radicals in the atmosphere.     

使用添加剂调质钙基脱硫剂的机理概述

从干法固硫气扩散及气固反应角度回顾了添加剂对钙基脱硫剂调质作用的有关研究情况,指出目前该技术在研究以及工业应用中存在的一些关键问题,并讨论该技术的发展趋势。     

Bacteria inactivation by sulfate radical: progress and non-negligible disinfection by-products

● Status of inactivation of pathogenic microorganisms by SO₄^•− is reviewed. ● Mechanism of SO₄^•− disinfection is outlined. ● Possible generation of DBPs during disinfection using SO₄^•− is discussed. ● Possible problems and challenges of using SO₄^•− for disinfection are presented. Sulfate radicals have been increasingly used for the pathogen inactivation due to their strong redox ability and high selectivity for electron-rich species in the last decade. The application of sulfate radicals in water disinfection has become a very promising technology. However, there is currently a lack of reviews of sulfate radicals inactivated pathogenic microorganisms. At the same time, less attention has been paid to disinfection by-products produced by the use of sulfate radicals to inactivate microorganisms. This paper begins with a brief overview of sulfate radicals’ properties. Then, the progress in water disinfection by sulfate radicals is summarized. The mechanism and inactivation kinetics of inactivating microorganisms are briefly described. After that, the disinfection by-products produced by reactions of sulfate radicals with chlorine, bromine, iodide ions and organic halogens in water are also discussed. In response to these possible challenges, this article concludes with some specific solutions and future research directions.