高压脉冲电晕处理发动机尾气中的NO的实验研究

本文通过对高压脉冲电晕放电产生的等离子体活性物质对发动机尾气中的NO进行活化，研究其净化率与电压、频率、风速以及初始浓度的关系及其相互之间的影响，同时研究NO的产物NO2随电压、频率、风速以及初始浓度的生成关系，实验表明，NO的净化率能够达到50％以上，在风速不大的条件下，NO转化的主要产物为NO2。     

介质阻挡放电净化硫化氢气体的实验研究

采用介质阻挡放电等离子体技术净化恶臭气体硫化氢。考察了电压、频率、硫化氢初始浓度以及停留时间对硫化氢净化效果的影响。结果表明,介质阻挡放电可以有效消除硫化氢污染,硫化氢净化率随电压、频率以及停留时间的增加而升高,随硫化氢初始浓度增加而下降。当电压≥19kV,频率为300Hz,停留时间为1.56s,硫化氢初始质量浓度为30.1mg/m3时,硫化氢净化率接近100%。     

低温等离子体治理H2S污染的实验研究

低温等离子体技术是一种高效、快速的污染消除技术,国内外都在对其进行广泛而深入的研究.采用脉冲电晕放电等离子体对空气中的硫化氢进行降解研究,探索了、脉冲峰压、脉冲频率、气体流量以及气体初始浓度对净化效果的影响,气体浓度由气相色谱仪测定.结果表明,脉冲电晕放电可以有效消除硫化氢污染,净化率随脉冲峰压和脉冲频率的增加而提高,随气体初始浓度和流量的增加而下降,且在初始浓度360 mg/m3、流量1200 mL/min、脉冲峰压30 kV、脉冲频率80 Hz的条件下,处理后的气体中已检测不到H2S,根据色谱检测限(0.29 mg/m3)计算出的净化率≥99.92%.采用离子色谱对产物进行了定性分析,发现H2S经放电处理后主要产物为SO2和SO3.     

低温等离子体治理H2S污染的实验研究

低温等离子体技术是一种高效、快速的污染消除技术，国内外都在对其进行广泛而深入的研究。采用脉冲电晕放电等离子体对空气中的硫化氢进行降解研究，探索了、脉冲峰压、脉冲频率、气体流量以及气体初始浓度对净化效果的影响，气体浓度由气相色谱仪测定。结果表明，脉冲电晕放电可以有效消除硫化氢污染，净化率随脉冲峰压和脉冲频率的增加而提高，随气体初始浓度和流量的增加而下降，且在初始浓度360mg／m^2、流量1200mL／min、脉冲峰压30kV、脉冲频率80Hz的条件下，处理后的气体中已检测不到H2S，根据色谱检测限（0．29mg／m^3）计算出的净化率≥99．92％。采用离子色谱对产物进行了定性分析，发现H2S经放电处理后主要产物为SO2和SO3。     

组合式脉冲电晕反应器处理二氯甲烷废气实验研究

利用线-板和线-筒式串联成组合式脉冲电晕反应器对二氯甲烷(DCM)的降解效果进行了研究,考察了脉冲电源参数、DCM初始浓度、气体流量以及载气等因素对去除效果的影响。结果表明:DCM的去除效果与脉冲高压电源的峰值电压和脉冲频率成正比,与其自身初始浓度和气体流量成反比。在空气作为载气、峰值电压22.5kV、脉冲频率50 Hz、DCM初始质量浓度300mg/m3和气体流量1.2L/min时,DCM的去除率可达到79.5%;傅立叶红外光谱检测可知,主要产物为CO2、N2O、COCl2、CO和H2O等。     

和田绿洲沙尘暴强度及其影响因子分析——以墨玉县为例

以和田绿洲西北部的墨玉县为研究区域,对该地区2016—2018年发生的沙尘暴天气资料以及气象因子(气温、风速、湿度、气压、水汽压、日照时数)和大气污染物(PM2.5、PM10、SO2、NO2、CO、O3)进行分析。结果表明,墨玉县沙尘暴天气主要发生在春夏季(3—8月),平均占全年发生频率的77.12%。墨玉县沙尘暴强度主要由气象因子决定,特别是气温、风速、日照时数和湿度。沙尘暴强度与大气颗粒物(PM10和PM2.5)存在着明显的间接关系,主要因为两者均受风速影响较大,沙尘暴强度越大,大气中PM10和PM2.5浓度越高。沙尘暴强度与SO2、NO2、CO、O3等大气污染物的关系非常微弱,但O3与沙尘暴的形成季节比较一致。     

脉冲电晕低温等离子体提高一氧化氮氧化效率的实验研究

提高一氧化氮（NO）的氧化效率对于提高生物法处理该类废气的净化效率具有重要意义。实验研究了低温等离子体在脉冲电晕条件下氧化废气中NO的过程,考察了不同峰值电压、氧气含量、气体停留时间和添加有机物等因素对提高NO氧化效率的影响。结果表明：低温等离子法可有效地提高NO的氧化效率,主要产物为NO₂;室温条件下,当进气NO浓度590 mg/m³、脉冲频率50 Hz时,增大峰值电压、气体停留时间和进气中的氧气含量可提高NO的氧化效率;在最适峰值电压15 kV,气体停留时间5 s时,NO氧化效率为20%;在进气NO中添加甲苯、乙醇后,NO氧化效率可增加至30%以上,甲苯的效果要好于乙醇。     

多针-板脉冲放电处理模拟尾气中的NO_x

机动车尾气中NO_x受到人们普遍关注。采用多针-板放电反应器,研究NO_x浓度变化随电气、气体等参数的变化规律,为脉冲放电去除NO_x提供一定理论支撑。结果表明:在一定条件下提高脉冲电压有利于NO转化;脉冲重复频率增大可提升NO_x去除率,脉冲重复频率达到一定值时NO_x去除率增幅不明显;流量增大利于NO转化,不利于NO_x去除;随氧浓度的升高NO转化率呈现先降低后升高,NO_x去除率逐渐降低。当氧浓度低于5%时,NO_x主要是通过NO还原成N_2;氧浓度高于5%时,NO主要通过氧化转化为NO_2。     

隔膜电解海水氧化耦合吸收脱硫脱硝净化船舶尾气技术

采用隔膜电解技术对海水进行改性,生成的氧化液和碱性液分别喷淋进入氧化洗涤塔和碱式吸收塔,通过耦合的二段式反应研究脱除模拟船舶尾气中NO与SO_2的性能,实验详细考察了NO与SO_2的气体流量与初始浓度、海水电解时间和氧化液有效氯浓度对SO_2和NO脱除效率的影响。结果表明:隔膜电解海水能够高效地脱除船舶尾气中的SO_2和NO;SO_2脱除效率高,在实验条件范围内几乎不受各因素的影响;NO脱除效率随NO初始浓度、海水电解时间、氧化液有效氯浓度的提升而增大,随SO_2初始浓度、气体流量的提升而减小。当气体流量为1 m~3·h~(-1),初始SO_2、NO浓度分别为600mL·m~(-3)和900 mL·m~(-3),海水电解时间为60 min,氧化液有效氯浓度为540 mg·L~(-1)时,模拟船舶尾气中SO_2和NO的去除效率可以分别达到98.6%和84.4%。     

ClO_2气相氧化联合CaCO_3浆液吸收同时脱硫脱硝试验研究

采用ClO_2气相氧化联合CaCO_3浆液吸收工艺对模拟烟气进行同时脱硫脱硝,研究了ClO_2/NO摩尔比、SO_2初始浓度对气相氧化段NO氧化率的影响及液相吸收段中CaCO_3浆液pH、温度和液气比对同时脱硫脱硝效果的影响。结果表明,在气相氧化段,NO的氧化率随着ClO_2/NO摩尔比的增加呈先快速增加后逐渐平稳的变化趋势;在给定的ClO_2/NO摩尔比(0.8)下,随着SO_2初始浓度的增加,NO氧化率稍有下降,高浓度SO2的存在对ClO_2氧化NO的抑制作用有限,说明ClO_2对NO的氧化反应具有良好的选择性。ClO_2气相氧化联合CaCO_3浆液吸收工艺最优反应条件:ClO_2/NO摩尔比为0.8,CaCO_3浆液初始pH为7.0、温度为55℃,液气比为18L/m3。当SO2初始质量浓度为1 000 mg/m~3、NO_x初始质量浓度为509 mg/m3时,最佳反应条件下SO_2去除率达100.00%,NO_x去除率达81%左右。     

循环水养殖系统中流化床生物滤器净水效果影响因素

为优化流化床生物滤器的工作性能,采用新型填料玻璃珠作为滤器的基质,并将其应用于罗非鱼循环水养殖系统,研究了玻璃珠粒径、床层膨胀率、碱度和氨氮负荷4个可控因素对其处理养殖废水效果的影响。结果表明,流化床生物滤器挂膜23d后生物膜成熟稳定,当床层膨胀率低于160％时,床层增高和填料流失现象不明显。选用0．2～0．4mm粒径的玻璃珠为填料时,对TAN和NO2--N的去除率显著高于以0．4～0．6mm玻璃珠为填料的滤器;随着床层膨胀率的提高,滤器对TAN和NO2--N的去除率逐渐下降,但对TAN的去除负荷有一定的提高;碱度和TAN负荷的增加有利于滤器的硝化作用。流化床生物滤器对养殖水体中的TAN的平均去除负荷和NO2--N的去除率分别可以达到（673．11±23．26）g／（m3·d）和（90．24±3．45）％,显示出较好的硝化性能。     

低温净化氮氧化物的改性活性炭材料

针对活性炭室温净化NO₂过程中生成NO的问题,分别用还原性物质和强氧化性物质对活性炭进行了改性研究,并分析了NO的生成原因和各种改性材料处理氮氧化物的作用机理。金属氧化物改性活性炭性能最好,室温条件下,对NO₂的净化效率在20 h内保持在98%以上,NO生成量为活性炭处理时的1/2弱。     

OH-initiated oxidation of DMS/DMSO: reaction products at high NOx levels

Dimethylsulphide (DMS) gas phase oxidation with OH radicals was investigated by long path FT-IR spectroscopy and by ion chromatography (IC) and HPLC-MS2 to quantify the reaction products and evaluate heterogeneous processes. The experiments were performed considering two different NOx (NO2+NO) levels. The initial concentration of NO2 was varied from 24 ppbV (NOx=1 ppmV) to 953 ppbV (NOx=10 ppmV). Photolysis of H2O2 was used as the OH-radical source. SO2, dimethylsulphoxide (DMSO), dimethylsulphone (DMSO2), methanesulphonic acid (MSA), methanesulphinic acid (MSIA) and methane sulphonyl peroxynitrate (MSPN) were identified as the main sulphur-containing products. The results indicate that higher NOx levels play a significant role in the chemistry of CH3S(O)x radical, influencing both the SO2/MSPN ratio and the amount of the sulphur species in the condensed phase, and that the NO2/NO ratio could influence the trends in the molar yields of the different products. For this reason the NOx content results a limiting parameter when on measure DMS in atmospheric environment.     

Short-term effects of gaseous pollutants on cause-specific mortality in Wuhan, China

In Asia, limited studies have been published on the association between daily mortality and gaseous pollutants of nitrogen dioxide (NO2), ozone (O3), and sulfur dioxide (SO2). Our previous studies in Wuhan, China, demonstrated long-term air pollution effects. However, no study has been conducted to determine mortality effects of air pollution in this region. This study was to determine the acute mortality effects of the gaseous pollutants in Wuhan, a city with 7.5 million permanent residents during the period from 2000 to 2004. There are approximately 4.5 million residents in Wuhan who live in the city's core area of 201 km2, where air pollution levels are highest, and pollution ranges are wider than the majority of the cities in the published literature. We used the generalized additive model to analyze pollution, mortality, and covariate data. We found consistent NO2 effects on mortality with the strongest effects on the same day. Every 10-microg/m3 increase in NO2 daily concentration on the same day was associated with an increase in nonaccidental (1.43%; 95% confidence interval [CI]: 0.87-1.99%), cardiovascular (1.65%; 95% CI: 0.87-2.45%), stroke (1.49%; 95% CI: 0.56-2.43%), cardiac (1.77%; 95% CI: 0.44-3.12%), respiratory (2.23%; 95% CI: 0.52-3.96%), and cardiopulmonary mortality (1.60%; 95% CI: 0.85-2.35%). These effects were stronger among the elderly than among the young. Formal examination of exposure-response curves suggests no-threshold linear relationships between daily mortality and NO2, where the NO2 concentrations ranged from 19.2 to 127.4 microg/m3. SO2 and O3 were not associated with daily mortality. The exposure-response relationships demonstrated heterogeneity, with some curves showing nonlinear relationships for SO2 and O3. We conclude that there is consistent evidence of acute effects of NO2 on mortality and suggest that a no-threshold linear relationship exists between NO2 and mortality.     

利用无泵水幕废气净化器治理高浓度NOx的工程实践

介绍了无泵水幕废气净化器的工作原理和运行特点,采用该设备处理某金刚石公司的酸洗车间高浓度的NOx气体,其净化效率达90%以上,净化后的NOx气体可直接达标排放.无泵水幕废气净化器解决了传统的水喷淋塔普遍存在的喷嘴堵塞、单级净化效率低、运行费用高等问题,在高浓度酸性气体治理方面具有很好的推广应用前景.     

用活性填料催化氧化-硝酸吸收法脱除氮氧化物的研究

为了提高硝酸吸收氮氧化物的效率，对活性填料催化氧化-硝酸吸收NOx进行了研究。结果表明：活性填料能明显提高NOx的吸收效率；当NOx中NO2体积百分含量增加，其吸收效率增加；随进气浓度和液气比的增大，NOx吸收效率增加；随NO2浓度的增加，NO的吸收效率先增加后减少，在NO／NO2为3时，NO吸收效率最高；随NO的增加NO2的吸收效率先增加后减少，在NO／NO2为0．6～1之间，NO2的吸收效果较好。     

负载IB族金属海泡石吸附NO性能的研究

采用浸渍法制备了负载IB族元素的系列金属基海泡石,用气相色谱等手段对制得的金属基海泡石对NO的吸附性能进行研究,并且对灼烧温度、金属负载量、分散度和压力等影响因素进行了讨论。实验结果表明,经过酸改性、负载金属后的海泡石对NO的吸附能力比原矿有很大的提高;选择出Cu/海泡石的最佳灼烧温度为300℃,最佳Cu负载量为5％;并证明在实验条件下Cu/海泡石上的NO吸附符合经验吸附等温式。     

The electrochemical selective reduction of NO using CoSe2@CNTs hybrid

Converting the NO from gaseous pollutant into NH₄ ⁺ through electrocatalytical reduction using cost-effective materials holds great promise for pollutant purifying and resources recycling. In this work, we developed a highly selective and stable catalyst CoSe₂ nanoparticle hybridized with carbon nanotubes (CoSe₂@CNTs). The CoSe₂@CNTs hybrid catalysts performed an extraordinary high selectivity for NH₄ ⁺ formation in NO electroreduction with minimal N₂O production and H₂ evolution. The specific spatial structure of CoSe₂ is conductive to the predominant formation of N-H bond between the N from adsorbed NO and H and inhibition of N-N formation from adjacent adsorbed NO. It was also the first time to convert the coordinated NO into NH₄ ⁺ using non-noble metal catalysis. Moreover, the original concept of employing CoSe₂ as eletrocatalyst for NO hydrogenation presented in this work can broaden horizons and provide new dimensions in the design of new highly efficient catalysts for NH₄ ⁺ synthesis in aqueous solution.

     

负载型Mn-Ce／TiO2催化剂的制备及其低温脱硝活性

以成型TiO2作为载体,通过浸渍法制备了Mn-Ce／TiO2低温SCR催化剂,并系统研究了制备方法、煅烧条件、活性组分担载量、Mn含量等参数对催化剂催化还原NO性能的影响。结果表明,煅烧温度的升高会促使活性组分结晶度的提高,从而引起催化活性的降低,在500℃和600℃下所得Mn-Ce／TiO2催化剂活性组分为无定型态,表现出较高的脱硝活性。活性组分担载量的增加有利于催化活性的提高。Mn含量对Mn-Ce／TiO2催化剂的活性有较大影响,当Mn／（Mn＋Ce）摩尔比为40％和85％时,催化剂活性最高。     

Characteristic behavior of peroxyacetyl nitrate (PAN) in Seoul megacity, Korea

We measured the concentrations of peroxyacetyl nitrate (PAN) and other photochemically reactive species, including O(3), NO(2), and non-methane hydrocarbons (NMHCs), in the Seoul Metropolitan area (SMA) during May through June in 2004 and 2005. PAN was determined using a fast chromatograph with luminol-based chemiluminescence detection. Mixing ratios of PAN ranged from below the detection limit (0.1ppbv) to 10.4ppbv with an average of 0.8ppbv. O(3) concentrations ranged from 0 to 141ppbv. The average PAN/O(3) ratio of 0.07 was higher than that observed in cities of Europe and North America (0.02) where control strategies have been enforced to reduce hydrocarbon emissions through extensively reformulated gasoline programs. Strong positive correlations between daily PAN and O(3) maxima during the day demonstrate that similar photochemical factors controlled the production of these two chemicals. However, relationships between PAN and its precursors, NO(2) and NMHCs, suggest that PAN production was more sensitive to NO(2) than NMHCs levels whereas O(3) production was limited by the overall availability of NMHCs. It is likely that the compositions of NMHCs in SMA were favorable for PAN production because of the low fractions of oxygenated compounds in automobile fuels. PAN maxima were observed around noon, which was 2-3h earlier than the much broader O(3) maxima that occurred in the midafternoon. After reaching the maximum, PAN concentrations rapidly dropped within a few hours, which could be largely due to thermal destruction and to limited production under the typically low NO(2) levels that occurred in the early afternoon. The heterogeneous destruction of particulate matter could be an additional sink for PAN in SMA.