活性焦表面性质对CUO/AC脱硫性能的影响

分别以不同浓度的硝酸处理活性焦载体,采用硝酸铜溶液浸渍法制备CuO/AC催化剂,利用BET、FT-IR和XRD等方法对载体及催化剂进行表征.考察了不同浓度的硝酸处理对活性焦载体性质的影响,并对制得的催化剂的脱硫性能进行了比较.结果表明,活性焦经过硝酸处理后孔结构参数变化很小,而表面含氧酸性官能团的含量有了很大的提高,使...     

铜铈掺杂六铝酸盐的脱硝性能

用共沉淀法制备用于脱除NO的六铝酸盐催化剂LaMxAl12-xO19(M =Cu,Ce,CuCe).用XRD、H2-TPR和BET对催化剂进行了结构和物性表征.用微型催化反应装置考察了催化剂在CO选择性催化还原NO中的活性.结果表明,Cu离子易于进入六铝酸盐晶格内,形成完整的六铝酸盐结构.Ce离子不易于进入六铝酸盐晶格内,主要以CeO2的形式存在.在CO+ NO条件下,3种催化剂都表现出较好的脱硝活性,LaCuCeAl10O19中由于Cu离子与Ce离子间产生协同作用,该催化剂的脱硝活性有所增加.加入SO2后,3种催化剂都有不同程度的失活现象发生,其中LaCuAl11O19催化剂受SO2中毒影响最严重,LaCuCeAl10O19催化剂的脱硝活性在三者中最好.     

Study on the removal of elemental mercury from simulated flue gas by Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-CeO<Subscript>2</Subscript>/AC at low temperature

Fe₂O₃ and CeO₂ modified activated coke (AC) synthesized by the equivalent-volume impregnation were employed to remove elemental mercury (Hg⁰) from simulated flue gas at a low temperature. Effects of the mass ratio of Fe₂O₃ and CeO₂, reaction temperature, and individual flue gas components including O₂, NO, SO₂, and H₂O (g) on Hg⁰ removal efficiency of impregnated AC were investigated. The samples were characterized by Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Results showed that with optimal mass percentage of 3 % Fe₂O₃ and 3 % CeO₂ on Fe3Ce3/AC, the Hg⁰ removal efficiency could reach an average of 88.29 % at 110 °C. Besides, it was observed that O₂ and NO exhibited a promotional effect on Hg⁰ removal, H₂O (g) exerted a suppressive effect, and SO₂ showed an insignificant inhibition without O₂ to some extent. The analysis of XPS indicated that the main species of mercury on used Fe3Ce3/AC was HgO, which implied that adsorption and catalytic oxidation were both included in Hg⁰ removal. Furthermore, the lattice oxygen, chemisorbed oxygen, and/or weakly bonded oxygen species made a contribution to Hg⁰ oxidation.     

燃煤烟气低温SCR脱硝中试研究

低温选择性催化还原(SCR)脱硝是国内外脱硝技术研发的热点,但目前主要集中在实验室小试范围,无法完全反映催化剂在实际烟气中的运行状况。在30 t/h循环流化床燃煤锅炉脱硫除尘装置后建设了2 000~5 000 m3/h的SCR脱硝中试装置,经系统研究发现,中试使用的蜂窝式催化剂对SO2和NO具有很强的吸附能力,且反应温度、喷氨速率和气体空速均会影响催化脱硝效率。为期5 d的连续运行实验结果表明,催化剂的脱硝效率一直稳定在30%~50%,并未发现明显的失活,这证明设计除雾除尘器、较大的混合器、混合器与反应器间较长的管路均有利于缓解催化剂因SO2、H2O和飞灰中的碱性金属导致的失活。     

Direct N2O decomposition over La2NiO4-based perovskite-type oxides

Direct decomposition of N₂O by perovskite-structure catalysts including La₂NiO₄, LaSrNiO₄, and La_0.7Ce_0.3SrNiO₄ was investigated. The catalysts were prepared by the Pechini method and characterized by x-ray diffraction (XRD), BET, scanning electron microscopy (SEM), and O₂-TPD. Experimental results indicate that the properties of La₂NiO₄ are significantly improved by partially substituting La with Sr and Ce. N₂O decomposition efficiencies achieved with LaSrNiO₄ and La_0.7Ce_0.3SrNiO₄ are 44 and 36%, respectively, at 400ºC. As the temperature was increased to 600ºC, N₂O decomposition efficiency achieved with LaSrNiO₄ and La_0.7Ce_0.3SrNiO₄ reached 100% at an inlet N₂O concentration of 1,000 ppm, while the space velocity was fixed at 8,000 hr^?1. In addition, effects of various parameters including oxygen, water vapor, and space velocity were also explored. The results indicate that N₂O decomposition efficiencies achieved with LaSrNiO₄ and La_0.7Ce_0.3SrNiO₄ are not significantly affected as space velocity is increased from 8,000 to 20,000 hr^?1, while La_0.7Ce_0.3SrNiO₄ shows better tolerance for O₂ and H₂O_(g). On the other hand, N₂ yield with LaSrNiO₄ as catalyst can be significantly improved by doping Ce. At a gas hour space velocity of 8,000 hr^?1, and a temperature of 600ºC, high N₂O decomposition efficiency and N₂ yield were maintained throughout the durability test of 60 hr, indicating the long-term stability of La_0.7Ce_0.3SrNiO₄ for N₂O decomposition.

Implications:Nitrous oxide (N₂O) not only has a high global warming potential (GWP₁₀₀ = 310), but also potentially destroys ozone in the stratosphere. Pervoskite-type catalysts including La₂NiO₄, LaSrNiO₄, and La_0.7Ce_0.3SrNiO₄ are applied for direct N₂O decomposition. The results show that N₂O decomposition can be enhanced as Sr and Ce are doped into La₂NiO₄. At 600ºC, N₂O decomposition efficiencies achieved with LaSrNiO₄ and La_0.7Ce_0.3SrNiO₄ reach 100%, demonstrating high activity and good potential for direct N₂O decomposition. Effects of O₂ and H₂O_(g) contents on catalytic activities are also evaluated and discussed.     

Trends and Relationships of O3, NOx and HC in the South Coast Air Basin of California

A basin-wide air quality trend analysis for the South Coast Air Basin of California is conducted for hydrocarbons (HC), NO_x, O₃ and CO using multi-station composite daily maximum-hour average ambient concentrations for the third quarter (July, August and September) from 1968 to 1985. Emissions and air quality trends are compared for the period 1968-1984. Ambient HC and NOX trends are somewhat different from estimated emission trends of HC and NO_x, while a definite, downward trend of ambient CO is consistent with vehicular emission control measures. Basin-wide ambient HC, NO_x and O₃ appear to show downward trends for the period 1970-1985, but because of high fluctuations it is difficult to delineate trends for shorter periods. The meteorology (850 mb temperature)-adjusted O₃ shows a more consistent downward trend than does unadjusted O₃. Polynomial and multiplicative regression models for basin-wide empirical O₃-HC-NO_x relationships Indicate that the O₃ variation is explained largely by the meteorological variable (850 mb temperature) although model estimations are improved by adding HC and NO_x concentration terms.     

Selective Reduction of Nitrogen Oxides In Combustion Flue Gases

The body of Information presented in this paper is directed to those Individuals concerned with the removal of NO_x in combustion flue gases. A catalytic process for the selective reduction of nitrogen oxides by ammonia has been investigated. Efforts were made toward the development of catalysts resistant to SO_x poisoning. Nitrogen oxides were reduced over various metal oxide catalysts in the presence or absence of SO_x(SO₂ and SO₃). Catalysts consisting of oxides of base metals (for example, Fe₂O₃) were easily poisoned by SO₃, forming sulfates of the base metals. A series of catalysts which are not susceptible to the SO_x poisoning has been developed. The catalysts possess a high activity and selectivity over a wide range of temperatures, 250—450°C. The catalysts were tested in a pilot plant which treated a flue gas containing 110-150 ppm NO_x, 660-750 ppm SO₂, and 40-90 ppm SO₃. The pilot plant was operated at 350°C and at a space velocity of 10,000 h^-1. The removal of nitrogen oxides was more than 90% for several months.

A mechanism of the NO-NH₃ reaction has also been investigated. It is found that NO reacts with NH₃ at a 1:1 mole ratio in the presence of oxygen and the reaction is completely inhibited by the absence of oxygen. The experimental data show that the NO-NH₃ reaction in the presence of oxygen is represented byNO + NH₃ + 1/4 O₂ = N₂ + 3/2 H₂O.     

Control of Diesel Gaseous and Particulate Emissions with a Tube-Type Wet Electrostatic Precipitator

Abstract

In this study, experiments were performed with a bench-scale tube-type wet electrostatic precipitator (wESPs) to investigate its effectiveness for the removal of mass- and number-based diesel particulate matter (DPM), hydrocarbons (HCs), carbon monoxide (CO), and oxides of nitrogen (NO_x) from diesel exhaust emissions. The concentration of ozone (O₃) present in the exhaust that underwent a nonthermal plasma treatment process inside the wESP was also measured. A nonroad diesel generator operating at varying load conditions was used as a stationary diesel emission source. The DPM mass analysis was conducted by means of isokinetic sampling and the DPM mass concentration was determined by a gravimetric method. An electrical low-pressure impactor (ELPI) was used to quantify the DPM number concentration. The HC compounds, n-alkanes, and polycyclic aromatic hydrocarbons (PAHs) were collected on a moisture-free quartz filter together with a PUF/XAD/PUF cartridge and extracted in dichloromethane with sonication. Gas chromatography (GC)/mass spectroscopy (MS) was used to determine HC concentrations in the extracted solution. A calibrated gas combustion analyzer (Testo 350) and an O₃ analyzer were used for quantifying the inlet and outlet concentrations of CO and NO_x (nitric oxide [NO] + nitrogen dioxide [NO₂]), and O₃ in the diesel exhaust stream. The wESP was capable of removing approximately 67–86% of mass- and number-based DPM at a 100% exhaust volumetric flow rate generated from 0- to 75-kW engine loads. At 75-kW engine load, increasing gas residence time from approximately 0.1 to 0.4 sec led to a significant increase of DPM removal efficiency from approximately 67 to more than 90%. The removal of n-alkanes, 16 PAHs, and CO in the wESP ranged from 31 to 57% and 5 to 38%, respectively. The use of the wESP did not significantly affect NO_x concentration in diesel exhaust. The O₃ concentration in diesel exhaust was measured to be less than 1 ppm. The main mechanisms responsible for the removal of these pollutants from diesel exhaust are discussed.     

活性焦和活性炭负载纳米铁处理TNT红水中的二硝基甲苯磺酸钠

以活性焦和活性炭为载体,采用液相还原法制备了负载纳米铁,比较了两种负载纳米铁对TNT红水中难降解物质二硝基甲苯磺酸钠(包括2,4-DNT-3-SO3Na和2,4-DNT-5-SO3Na)的去除能力。实验结果表明,作为负载材料活性焦的相对有效比表面积与孔体积要优于活性炭,而且有利于更好地发挥出负载纳米铁的优势。单位面积活性焦负载纳米铁去除2,4-DNT-5-SO3Na的能力明显高于活性炭负载纳米铁,单位面积活性焦负载纳米铁去除2,4-DNT-3-SO3Na的能力在较小投加量条件下高于活性炭负载纳米铁,但均随投加量的增加而下降;而对于活性炭负载纳米铁,其单位面积去除能力基本不受投加量的影响,而且对二硝基甲苯磺酸钠的去除率高于活性焦负载纳米铁。耦合混凝沉淀的总去除效果表明,单位面活性焦负载纳米铁对2,4-DNT-5-SO3Na的去除能力高于活性炭负载纳米铁,而对2,4-DNT-3-SO3Na的去除能力则低于活性炭负载纳米铁。     

活性焦吸附处理一硝基甲苯(MNT)废水

一硝基甲苯(MNT)废水是一种具有高毒性、难降解的火炸药废水。以活性焦为吸附剂,研究了活性焦对MNT废水中COD的吸附性能及pH、时间、温度和活性焦用量对吸附效果的影响,并分析了吸附前后MNT废水水质和急性毒性的变化。实验结果表明,pH、时间和活性焦用量是影响吸附效果的主要因素,吸附过程符合拟二级动力学,吸附速率常数为1.01×10-2g/(mg·min),可以用Freundlich吸附等温线来描述,等温线常数为Kf=1.14×10-4,n=0.58;在pH为3,温度为20℃,活性焦用量为80g/L的条件下吸附MNT废水3 h,COD的去除率达到72.0%,急性毒性下降了98.6%,表明活性焦能有效地吸附处理MNT废水。     

Fenton氧化法同时脱硫脱硝的实验研究

应用Fenton液相氧化吸收法进行同时脱硫脱硝实验。首先,利用单因素实验,分别考察了H2O2浓度、Fe2+投加量、初始pH值、UV照射和温度对脱硫脱硝的影响。结果表明,SO2和NO去除率随着H2O2浓度和Fe2+投加量的增大而提高;初始pH对SO2和NO的去除有较大影响;UV能促进SO2和NO的净化;温度对脱硫效率影响不大,但对NO的去除有显著作用,适当升温可以提高脱硝效率。随后,考察了SO2对NO去除率的影响。通过单独脱硝和同时脱硫脱硝的对比实验发现,SO2的加入对NO的去除有一定的促进作用,Fenton法可同时获得起始约80%的脱硝效率和98%以上的脱硫效率。     

Ground level ozone concentrations and its association with NOx and meteorological parameters in Kathmandu valley, Nepal

This paper summarizes the results of a yearlong continuous measurements of gaseous pollutants, NO, NO₂, NO_x and O₃ in the ambient air at Kathmandu valley. Measured concentration of the pollutants in study area is a function of time. NO, NO₂ and O₃ peak occurred in succession in presence of sunlight. At the time of maximum O₃ concentration most of the NO_x are utilized. The diurnal cycle of ground level ozone concentrations, revealed mid-day peak with lower nocturnal concentrations and inverse relationship exists between O₃ and NO_x, which are evidences of photochemical O₃ formation. The observed ground level ozone during monsoon is slight lower than the pre-monsoon value. Further, lack of rainfall and higher temperature, solar radiation in the pre-monsoon have given rise to the gradual build up of ozone and it is lowest during winter. Ground level ozone concentrations measured during bandha (general strike) and weekend are 19% and 13% higher than those measured during weekdays. The most effective ozone abatement strategy for Kathmandu Valley may be control of NO_x emissions.     

Ultra-high adsorption of Hg0 using impregnated activated carbon by selenium

Activated carbon was one of the main adsorptions utilized in elemental mercury (Hg⁰) removal from coal combustion flue gas. However, the high cost and low physical adsorption efficiency of activated carbon injection (ACI) limited its application. In this study, an ultra-high efficiency (nearly 100%) catalyst sorbent-Se_x/Activated carbon (Se_x/AC) was synthesized and applied to remove Hg⁰ in the simulated flue gas, which exhibited 120 times outstanding adsorption performance versus the conventional activated carbon. The Se_x/AC reached 17.98 mg/g Hg⁰ adsorption capacity at 160 °C under the pure nitrogen atmosphere. Moreover, it maintained an excellent mercury adsorption tolerance, reaching the efficiency of Hg⁰ removal above 85% at the NO and SO₂ conditions in a bench-scale fixed-bed reactor. Characterized by the multiple methods, including BET, XRD, XPS, kinetic and thermodynamic analysis, and the DFT calculation, we demonstrated that the ultrahigh mercury removal performance originated from the activated Se species in Se_x/AC. Chemical adsorption plays a dominant role in Hg⁰ removal: Selenium anchored on the surface of AC would capture Hg⁰ in the flue gas to form an extremely stable substance-HgSe, avoiding subsequent Hg⁰ released. Additionally, the oxygen-containing functional groups in AC and the higher BET areas promote the conversion of Hg⁰ to HgO. This work provided a novel and highly efficient carbon-based sorbent -Se_x/AC to capture the mercury in coal combustion flue gas.

Selenium-modified porous activated carbon and the interface functional group promotes the synergistic effect of physical adsorption and chemical adsorption to promote the adsorption capacity of Hg⁰.

     

Effect of Hydrocarbon and NO x on Photochemical Smog Formation under Simulated Transport Conditions

The body of information presented in this paper is directed to those individuals concerned with the effect of urban pollution on downwind areas. Concern has been expressed over the appropriate hydrocarbon and NO _x control strategy to be used in minimizing the effects of ozone and NO₂ on urban population centers and their downwind environs. O₃ and NO₂ formation were studied in smog chamber irradiations as a function of the initial NO _x concentration at three hydrocarbon concentrations. By carrying out the irradiations for a period of time equivalent to one solar day in a continuously diluting system, smog formation in a chemically reacting pollutant system under transport was simulated. The results of this experimental simulation suggest that hydrocarbon reduction reduces O₃ in urban as well as downwind areas while NO _x reduction increases O₃ in the urban area and has little effect on O₃ in downwind areas. Both hydrocarbon and NO _x reduction will reduce atmospheric NO₂ levels, with the effect of NO _x reduction generally being more pronounced.     

Degradation of bisphenol A in aqueous solution by persulfate activated with ferrous ion

Degradation of bisphenol A (BPA) in aqueous solution was studied with high-efficiency sulfate radical (SO₄ ^?·), which was generated by the activation of persulfate (S₂O₈ ^2?) with ferrous ion (Fe²⁺). S₂O₈ ^2? was activated by Fe²⁺ to produce SO₄ ^?·, and iron powder (Fe⁰) was used as a slow-releasing source of dissolved Fe²⁺. The major oxidation products of BPA were determined by liquid chromatography-mass spectrometer. The mineralization efficiency of BPA was monitored by total organic carbon (TOC) analyzer. BPA removal efficiency was improved by the increase of initial S₂O₈ ^2? or Fe²⁺ concentrations and then decreased with excess Fe²⁺ concentration. The adding mode of Fe²⁺ had significant impact on BPA degradation and mineralization. BPA removal rates increased from 49 to 97 % with sequential addition of Fe²⁺, while complete degradation was observed with continuous diffusion of Fe²⁺, and the latter achieved higher TOC removal rate. When Fe⁰ was employed as a slow-releasing source of dissolved Fe²⁺, 100 % of BPA degradation efficiency was achieved, and the highest removal rate of TOC (85 %) was obtained within 2 h. In the Fe⁰–S₂O₈ ^2? system, Fe⁰ as the activator of S₂O₈ ^2? could offer sustainable oxidation for BPA, and higher TOC removal rate was achieved. It was proved that Fe⁰–S₂O₈ ^2? system has perspective for future works.     

NOX Levels in the Caracas Valley

An analysis of air quality data from 1970-1975 in the Los Angeles (LA) Basin has been made with emphasis on factors relevant to high hourly NO₂ concentrations, (NO₂). Detailed analysis of CO and SO₂ air quality and the (NO _x )/(CO) and (CO)/(SO₂) ratios reveals that high (NO₂) result mainly from vehicular sources; contributions from stationary sources to these high (NO₂) of greater than 10% occur rarely. Meteorological conditions (very low early-morning inversion base height and low wind speed) favoring the formation of high (NO₂) restrict the impact of elevated point NO _x sources on the ground level (NO₂) during the early to mid-morning hours. The overnight leftover NO _x during high NO₂ days is shown to originate largely from local sources near the monitoring sites. A regression analysis using NO₂, NO _x and HC data from downtown LA shows that a 50% reduction in (NO _x ) reduces high (NO₂) by 40-45%; a 50% reduction in (HC) reduces high (NO₂) by 5-10%. The present analysis supports assumptions used in an earlier generalized rollback model that related NO _x emissions to high 1-h average (NO₂) observed at downtown LA.     

Characterizations of chemical oxidants in Mexico City: A regional chemical dynamical model (WRF-Chem) study

The formation of chemical oxidants, particularly ozone, in Mexico City were studied using a newly developed regional chemical/dynamical model (WRF-Chem). The magnitude and timing of simulated diurnal cycles of ozone (O₃), carbon monoxide (CO) and nitrogen oxides (NO_x)_, and the maximum and minimum O₃ concentrations are generally consistent with surface measurements. Our analysis shows that the strong diurnal cycle in O₃ is mainly attributable to photochemical variations, while diurnal cycles of CO and NO_x mainly result from variations of emissions and boundary layer height. In a sensitivity study, oxidation reactions of aromatic hydrocarbons (HCs) and alkenes yield highest peak O₃ production rates (20 and 18 ppbv h⁻¹, respectively). Alkene oxidations, which are generally faster, dominate in early morning. By late morning, alkene concentrations drop, and oxidations of aromatics dominate, with lesser contributions from alkanes and CO. The sensitivity of O₃ concentrations to NO_x and HC emissions was assessed. Our results show that daytime O₃ production is HC-limited in the Mexico City metropolitan area, so that increases in HC emissions increase O₃ chemical production, while increases in NO_x emissions decrease O₃ concentrations. However, increases in both NO_x and HC emissions yield even greater O₃ increases than increases in HCs alone. Uncertainties in HC emissions estimates give large uncertainties in calculated daytime O₃, while NO_x emissions uncertainties are less influential. However, NO_x emissions are important in controlling O₃ at night.     

Enhancement of nitric oxide decomposition efficiency achieved with lanthanum-based perovskite-type catalyst

Direct decompositions of nitric oxide (NO) by La_0.7Ce_0.3SrNiO₄, La_0.4Ba_0.4Ce_0.2SrNiO₄, and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ are experimentally investigated, and the catalysts are tested with different operating parameters to evaluate their activities. Experimental results indicate that the physical and chemical properties of La_0.7Ce_0.3SrNiO₄ are significantly improved by doping with Ba and partial substitution with Pr. NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ are 32% and 68%, respectively, at 400 °C with He as carrier gas. As the temperature is increased to 600 °C, NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, respectively, reach 100% with the inlet NO concentration of 1000 ppm while the space velocity is fixed at 8000 hr^?1. Effects of O₂, H₂O_(g), and CO₂ contents and space velocity on NO decomposition are also explored. The results indicate that NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, respectively, are slightly reduced as space velocity is increased from 8000 to 20,000 hr^?1 at 500 °C. In addition, the activities of both catalysts (La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄) for NO decomposition are slightly reduced in the presence of 5% O₂, 5% CO₂, or 5% H₂O_(g). For durability test, with the space velocity of 8000 hr^?1 and operating temperature of 600 °C, high N₂ yield is maintained throughout the durability test of 60 hr, revealing the long-term stability of Pr_0.4Ba_0.4Ce_0.2SrNiO₄ for NO decomposition. Overall, Pr_0.4Ba_0.4Ce_0.2SrNiO₄ shows good catalytic activity for NO decomposition.

Implications: Nitrous oxide (NO) not only causes adverse environmental effects such as acid rain, photochemical smog, and deterioration of visibility and water quality, but also harms human lungs and respiratory system. Pervoskite-type catalysts, including La_0.7Ce_0.3SrNiO₄, La_0.4Ba_0.4Ce_0.2SrNiO₄, and Pr_0.4Ba_0.4Ce_0.2SrNiO₄, are applied for direct NO decomposition. The results show that NO decomposition can be enhanced as La_0.7Ce_0.3SrNiO₄ is substituted with Ba and/or Pr. At 600 °C, NO decomposition efficiencies achieved with La_0.4Ba_0.4Ce_0.2SrNiO₄ and Pr_0.4Ba_0.4Ce_0.2SrNiO₄ reach 100%, demonstrating high activity and good potential for direct NO decomposition. Effects of O₂, H₂O_(g), and CO₂ contents on catalytic activities are also evaluated and discussed.     

Optimization of Reburning for Advanced N0x Control on Coal-fired Boilers

This paper summarizes an experimental study which was conducted to investigate the chemical constraints of the reburning process and identify reburning configurations for optimal NO_x reduction in coal-fired boilers. Tests were performed on a bench scale tunnel furnace to characterize and optimize the fuel-rich reburning zone and the fuel-lean burnout zone independently. Detailed measurements ofunburned hydrocarbons, CO, NH₃, and HCN were made at the reburning zone exit. The influence of the concentrations of reactive species was examined as were temperature effects for both the reburning and burnout zone. Results indicated that reburning zone chemistry was not rate limiting. The impacts of temperature and burnout zone oxidation were of major importance. Integration of the optimum reburning and burnout zone configurations resulted in increased NO_x reduction. Over 85 percent reduction in NO_x emissions was achieved with ammonium sulfate injection in the burnout zone under optimum reburning conditions.     

Analysis of the relationship between ambient levels of O3, NO2 and NO as a function of NOx in the UK

Monitoring data from the UK Automatic Urban and Rural Network are used to investigate the relationships between ambient levels of ozone (O₃), nitric oxide (NO) and nitrogen dioxide (NO₂) as a function of NO_x, for levels ranging from those typical of UK rural sites to those observed at polluted urban kerbside sites. Particular emphasis is placed on establishing how the level of ‘oxidant’, OX (taken to be the sum of O₃ and NO₂) varies with the level of NO_x, and therefore to gain some insight into the atmospheric sources of OX, particularly at polluted urban locations. The analyses indicate that the level of OX at a given location is made up of NO_x-independent and NO_x-dependent contributions. The former is effectively a regional contribution which equates to the regional background O₃ level, whereas the latter is effectively a local contribution which correlates with the level of primary pollution. The local oxidant source has probable contributions from (i) direct NO₂ emissions, (ii) the thermal reaction of NO with O₂ at high NO_x, and (iii) common-source emission of species which promote NO to NO₂ conversion. The final category may include nitrous acid (HONO), which appears to be emitted directly in vehicle exhaust, and is potentially photolysed to generate HO_x radicals on a short timescale throughout the year at southern UK latitudes. The analyses also show that the local oxidant source has significant site-to-site variations, and possible reasons for these variations are discussed. Relationships between OX and NO_x, based on annual mean data, and fitted functions describing the relative contributions to OX made by NO₂ and O₃, are used to define expressions which describe the likely variation of annual mean NO₂ as a function of NO_x at 14 urban and suburban sites, and which can take account of possible changes in the regional background of O₃.