降低FCC再生烟气NOx排放助剂的实验室评价

通过采用ACE装置与烟气NOx分析仪器联用的实验室评价方法,可在更接近实际催化裂化反应-再生过程的条件下,评价助剂对再生烟气中NOx的催化转化性能,同时还可考察助剂的加入对催化裂化产品分布的影响.采用该方法对几种降NOx助剂的性能进行了评价,结果表明,在催化剂体系中含有Pt基CO助燃剂的情况下,加入4%的RDNOx助剂后,烟气NOx降低幅度约30%～40%,且催化裂化产品分布基本不受影响.     

纳米氧化铈对汽油发动机尾气污染物排放的影响

通过非水微乳液法制备了纳米氧化铈，并将之添加到90^#汽油中，研究了纳米氧化铈对汽油动力性能、尾气污染物CO、HC、PM、NOx排放的影响。结果表明：非水微乳液法制备的纳米氧化铈粒径在30～50nm之间，粒径分布较窄；添加浓度为100mg／L时，不会对汽油的动力性能产生明显影响，但可以明显降低90。汽油尾气中的CO、HC、PM、NOx排放。其中，800r／min的正常怠速下可以降低CO排放19．39％、HE排放19．92％、NOx排放51．19％、PM排放25％；在2000r／min的高怠速下可降低CO排放16．17％、NOx排放46．92％、PM排放16．67％。     

Pt／MgO催化剂上NOx存储-还原反应性能

采用稀燃一富燃交替运行方式，研究存储一还原型催化剂PL／MgO的NOx存储性能以及C3H6还原NOx反应性能。氧化存储段，NOx可被有效存储；当氧化性气氛转换为还原性气氛后，出现一个NOx峰，降低了总的转化效果。NOx峰的大小与存储段和还原段时间之比、温度等因素有关；400℃时NOx峰最小，总转化率最高。5h循环实验表明，400℃时PL／MgO催化剂再生良好，NOx转化率稳定在96％。于反应气氛中添加100mg,／m^3SO2进行了5h抗硫性实验，Pt／MgO催化剂的抗硫中毒能力明显强于Pt／BaO／Al2O3。     

改性半焦脱除烟气中SO2的研究

对内蒙工业副产褐煤半焦（比表面积49.187m^2／g,孔容0.0351cm^2／g）,采用加压水热化学活化法,HNO3活化法和高温煅烧相结合的方法制备出半焦烟气脱硫剂,并对脱硫剂的脱硫性能进行固定床活性评价。分析表明,其脱硫效果比较好,转化率维持在50％以上的累计硫容可达24．30％,脱硫时间长达35h,远远高于原料半焦的脱硫效果（硫容为0．68％,时间为1．5h）;同时采用水洗法对脱硫剂进行再生,其再生液可用来制备浓度为9.01％的稀硫酸。     

FeSO4/Ac脱硫剂脱硫性能的研究

为寻找经济适用且具有较高效率的烟气脱硫方法．研制了FeSO4／Ac脱硫剂。并对FeSO4／Ac脱硫剂的脱硫性能进行了实验研究。实验研究结果显示,烟气中O2、水蒸气含量的多少及脱硫温度的高低会影响FeSO4／Ac脱硫剂的脱硫性能。实验证明,当n(O2):n(SO2)=7～10、n(H2O)：n(SO2)=3～5、脱硫温度取120℃时,FeSO4／Ac脱硫剂具有良好的脱硫性能,脱硫效率可达92．1％～96．8％。FeSO4／Ac脱硫剂能够再生重复使用。采用水蒸气加热再生法对FeSO4／Ac脱硫剂进行再生,实验结果显示,经4次加热法再生的FeSO4／Ac脱硫剂的脱硫效率仍能达到91％。     

燃煤锅炉烟气NOx污染等离子体治理技术

燃煤锅炉烟气NOx污染治理技术种类较多。本文综合评述了各种烟气NOx污染等离子体治理技术，重点介绍了电晕放电脱除烟气中NOx的最新研究成果。对燃煤锅炉烟气NOx污染治理技术的研究和开发具有实用价值。     

高活性脱硫剂脱硫工艺的实验研究

对以粉煤灰为原料制备的高活性脱硫剂进行了半干法烟气脱硫实验研究，考虑添加剂、脱硫剂加入量、反应温度、烟气流量工艺因素的影响时该活性脱硫剂的脱硫性能；实验结果表明，加入添加剂后，脱硫效率提高1．5％～8．1％；当烟气流量〈2m^3／min，钙硫比取1．5—2．0范围时，脱硫效率较高；一定范围内反应温度变化对脱硫效率影响不大。     

布袋协同粉体助剂对粘性微细粒子的过滤及反吹清灰实验研究

为了解决布袋除尘器对粘性微细粒子过滤效率低及粘性微细粒子粘附布袋造成反吹清灰困难的问题,在过滤面积为30 m2的布袋除尘器实验台上,研究了布袋外加粉体助剂过滤粘性微细粒子的新方法,用welas3000气溶胶粒径谱仪测试布袋除尘器上下游的粉尘浓度和粒径分布,探讨了粉体助剂层厚度、过滤速度以及布袋材质等对柴油机尾气颗粒物过滤效率及压降的影响,同时考察了粉体助剂层对布袋再生效率的影响。实验结果表明,(1)外加粉体助剂显著提高了过滤效率,在滤速0.2 m/min、粉体厚度1.0 mm时,对柴油机排气微粒(PM0.25)的过滤效率达99.92%~99.99%;(2)外加粉体助剂显著改善了布袋过滤粘性微细粒子的再生性能,再生效率可达到83.6%,而未外加粉体时布袋的再生效率仅有18.7%。外加粉体助剂有效地保护了布袋,使其免受粘性粒子的粘附和堵塞。     

SCR系统超洁净排放调整与出口NO_x均匀性分析

针对典型SCR系统普遍存在的出口烟道与烟囱处NOx在线监测值不一致的问题与超洁净排放要求,选择2台流场与喷氨格栅结构不同的SCR系统进行性能与优化调整实验。通过对喷氨格栅区域烟气分布与喷氨调整前后出口烟道内NOx分布的测试,分析了导致问题的原因与调整方案的有效性以及不同喷氨格栅结构的优劣性。结果表明:喷氨格栅区域烟气流场分布与区域喷氨量的不一致性是导致不同点位NOx浓度在线监测值不一致的原因;依据调整方案能有效实现SCR出口烟道内NOx浓度均匀分布与超洁净排放的要求;改造后,能针对烟道宽度方向上烟气不均现象进行区域喷氨量调整的喷氨格栅结构Ⅱ与更均匀的烟气分布,促使调整后的2号机组A、B两侧出口NOx浓度分布相对标准偏差明显优于1号机组。     

尿素和添加剂湿法烟气同时脱硫脱氮工艺研究(Ι)

对尿素和添加剂同时吸收烟气中 SO2 和 NOx 进行了实验研究。结果表明 ,烟气中 SO2 极易脱除 ,在实验条件下 SO2 脱除率均大于 99%,操作工艺条件变化主要是影响 NOx脱除率。尿素和添加剂质量分数对 NOx 脱除率影响较小 ,NOx脱除率随尿素和添加剂质量分数的增加而缓慢增加 ;吸收剂 p H和吸收反应温度对 NOx脱除率有显著影响 ,最佳 p H为 7,最佳反应温度为 70～80℃。     

Analysis of photochemical pollution in summer and winter using a photochemical box model in the center of Tokyo, Japan.

In order to give an effective and rapid analysis of the photochemical pollution and information for emission control strategies, a photochemical box model (PBM) was applied to one moderate summer episode, 11 July 1996, and one typical winter episode, 3 December 1996, in the center of Tokyo, Japan. The box model gave a good prediction of the photochemical pollution with minimal investment. As expected, the peak ozone in summer is higher than in winter. The NOx concentrations in winter are higher than those in summer. In summer, NO and NO2 have one peak in the morning. In winter, NO and NO2 show two peaks during the day. Three model runs including no reactions, a zero ozone boundary condition and dark reactions were conducted to understand the photochemical processes. The effects of emission reduction on the formation of the photochemical pollution in the center of Tokyo have been studied. The results show that the reduction of NMHC emission can decrease the ozone, however, the reduction of NOx emission can increase the ozone. It can be concluded that if the NOx emission are reduced, the reduction of NMHC should be more emphasized in order to decrease the ozone concentration in the center of Tokyo, Japan, especially the reduction of the NMHC from stationary source emission.     

Regional NOx emission inversion through a four-dimensional variational approach using SCIAMACHY tropospheric NO2 column observations

In this paper, the NOx emission scaling factors applied over the 2001 National Emissions Inventory (NEI) are estimated through a four-dimensional variational (4D-Var) approach using SCIAMACHY (Scanning Imaging Absorption spectroMeter for Atmospheric CHartographY) tropospheric NO₂ columns measured during summer 2004. In the “top-down” approach, two-month average NO₂ columns are assimilated into a regional chemical transport model (CTM), STEM, using different assimilation setups. In a basic setup, NOx emissions are adjusted by assimilating the NO₂ columns. A more general setup of emission inversion allows the initial O₃ concentrations be adjusted along with the NOx emissions. A final case is set up to assimilate both the NO₂ columns and O₃ measurement from various platforms while allowing adjustments of both the NOx emissions and the initial O₃ concentrations. It is found that the addition of O₃ measurements did not improve the NOx emission inversion. With the NOx emission at surface and upper levels being adjusted separately, results from four cases show that the elevated NOx emission reduction ranges from 8.9% to 11.4%, and the surface NOx emission reduction is up to 6.6%. All the cases show NOx emission reduction in Ohio valley and Washington, District of Columbia areas.     

煤粉再燃的半工业炉试验

从系统NOx还原效果，主燃区，再燃区和燃尽区内NOx的分解几方面对煤粉再燃效果进行半工业炉试验研究。虽然主燃区NOx生成量与主燃区过量空气系数成正比，系统NOx还原率却在主燃区过量空气系数一1．10时呈现最大值；再燃区还原性气氛有利于NOx的还原，但富氧氛围也可以实现一定NOx分解，燃尽区内煤粉异相还原占主要地位。以基础工况和再燃工况下的锅炉尾部NOx排放量的差值来计算系统NOx还原率可以更好地体现锅炉系统的再燃脱硝能力。     

Nitrogen oxides emission control options for coal-fired electric utility boilers

Recent regulations have required reductions in emissions of nitrogen oxides (NOx) from electric utility boilers. To comply with these regulatory requirements, it is increasingly important to implement state-of-the-art NOx control technologies on coal-fired utility boilers. This paper reviews NOx control options for these boilers. It discusses the established commercial primary and secondary control technologies and examines what is being done to use them more effectively. Furthermore, the paper discusses recent developments in NOx controls. The popular primary control technologies in use in the United States are low-NOx burners and overfire air. Data reflect that average NOx reductions for specific primary controls have ranged from 35% to 63% from 1995 emissions levels. The secondary NOx control technologies applied on U.S. coal-fired utility boilers include reburning, selective noncatalytic reduction (SNCR), and selective catalytic reduction (SCR). Thirty-six U.S. coal-fired utility boilers have installed SNCR, and reported NOx reductions achieved at these applications ranged from 15% to 66%. Recently, SCR has been installed at >150 U.S. coal-fired utility boilers. Data on the performance of 20 SCR systems operating in the United States with low-NOx emissions reflect that in 2003, these units achieved NOx emission rates between 0.04 and 0.07 lb/10(6) Btu.     

Modelling the spatial distribution of SO2 and NOx emissions in Ireland

The spatial distributions of sulphur dioxide (SO2) and nitrogen oxides (NOx) emissions are essential inputs to models of atmospheric transport and deposition. Information of this type is required for international negotiations on emission reduction through the critical load approach. High-resolution emission maps for the Republic of Ireland have been created using emission totals and a geographical information system, supported by surrogate statistics and landcover information. Data have been subsequently allocated to the EMEP 50 x 50-km grid, used in long-range transport models for the investigation of transboundary air pollution. Approximately two-thirds of SO2 emissions in Ireland emanate from two grid-squares. Over 50% of total SO2 emissions originate from one grid-square in the west of Ireland, where the largest point sources of SO2 are located. Approximately 15% of the total SO2 emissions originate from the grid-square containing Dublin. SO2 emission densities for the remaining areas are very low, < 1 t km-2 year-1 for most grid-squares. NOx emissions show a very similar distribution pattern. However, NOx emissions are more evenly spread over the country, as about 40% of total NOx emissions originate from road transport.     

Effectiveness of emission control technologies for auxiliary engines on ocean-going vessels

Large auxiliary engines operated on ocean-going vessels in transit and at berth impact the air quality of populated areas near ports. This paper presents new information on the comparison of emission ranges from three similar engines and the effectiveness of three control technologies: switching to cleaner burning fuels, operating in the low oxides of nitrogen (NOx) mode, and selective catalytic reduction (SCR). In-use measurements of gaseous (NOx, carbon monoxide [CO], carbon dioxide [CO2]) and fine particulate matter (PM2.5; total and speciated) emissions were made on three auxiliary engines on post-PanaMax class container vessels following the International Organization for Standardization-8178-1 protocol. The in-use NOx emissions for the MAN B&W 7L32/40 engine family vary from 15 to 21.1 g/kW-hr for heavy fuel oil and 8.9 to 19.6 g/kW-hr for marine distillate oil. Use of cleaner burning fuels resulted in NOx reductions ranging from 7 to 41% across different engines and a PM2.5 reduction of up to 83%. The NOx reductions are a consequence of fuel nitrogen content and engine operation; the PM2.5 reduction is attributed to the large reductions in the hydrated sulfate and organic carbon (OC) fractions. As expected, operating in the low-NOx mode reduced NOx emissions by approximately 32% and nearly doubled elemental carbon (EC) emissions. However, PM2.5 emission factors were nearly unchanged because the EC emission factor is only approximately 5% of the total PM2.5 mass. SCR reduced the NOx emission factor to less than 2.4 g/kW-hr, but it increased the PM2.5 emissions by a factor of 1.5-3.8. This increase was a direct consequence of the conversion of sulfur dioxide to sulfate emissions on the SCR catalyst. The EC and OC fractions of PM2.5 reduced across the SCR unit.     

Nitrogen oxides from waste incineration: control by selective non-catalytic reduction

An experimental study of the selective non-catalytic reduction (SNCR) process was carried out to determine the efficiency of NOx removal and NH3 mass balance, the NOx reducing reagent used. Experimental tests were conducted on a full-scale SNCR system installed in a hospital waste incineration plant. Anhydrous NH3 was injected at the boiler entrance for NOx removal. Ammonia was analyzed after each flue-gas treatment unit in order to establish its mass balance and NH3 slip in the stack gas was monitored as well. The effective fraction of NH3 for the thermal NOx reduction was calculated from measured values of injected and residual NH3. Results show that a NOx reduction efficiency in the range of 46.7-76.7% is possible at a NH3/NO molar ratio of 0.9-1.5. The fraction of NH3 used in NOx removal was found to decrease with rising NH3/NO molar ratio. The NH3 slip in the stack gas was very low, below permitted limits, even at the higher NH3 dosages used. No direct correlation was found between the NH3/NO molar ratio and the NH3 slip in the stack gas since the major part of the residual NH3 was converted into ammonium salts in the dry scrubbing reactor and subsequently collected in the fabric filter. Moreover, another fraction of NH3 was dissolved in the scrubbing liquor.     

Sensitivity of ozone to precursor emissions in urban Beijing with a Monte Carlo scheme

In order to understand the formation mechanisms of high surface ozone and identify the main contributor sources in Beijing, this study investigates the sensitivity of surface ozone to NO, NO₂ and nine types of NMVOC emissions during a photochemical smog episode. Monte Carlo sensitivity analysis scheme with fifty simulations is established based on the Nested Air Quality Prediction Model System (NAQPMS). At every simulation, each of the eleven precursor emissions is perturbed with a distinct set of perturbations. The sensitivities of ozone to emissions are identified by multiple linear regressions. The stability of sensitivity results is validated by two experiments with standard deviations of log-normal perturbations set as 30% and 50% respectively. The sensitivity results suggest that the current high surface ozone is strongly stimulated by NMVOC emissions. Among NMVOC emissions, formaldehyde, ethylene and olefins emissions present the greatest impacts on ozone. On the other hand, NOx emissions have a strong inhibitory effect on ozone formation, even after 50% NOx emission reduction. This indicates that the current ozone formation in Beijing is under NOx-saturated conditions. A transition of ozone formation is observed from NOx-saturated to NOx-limited sensitivity behavior with a 75% reduction of NOx emissions. This study gives the implication that abatement of the four NMVOC types mentioned above could be efficient on reducing the high levels of surface ozone in central urban Beijing, while inadequate abatement in NOx emissions probably induces reverse effects.     

Simultaneous control of Hg0, SO2, and NOx by novel oxidized calcium-based sorbents

Efforts to develop multipollutant control strategies have demonstrated that adding certain oxidants to different classes of Ca-based sorbents leads to a significant improvement in elemental Hg vapor (Hg0), SO2, and NOx removal from simulated flue gases. In the study presented here, two classes of Ca-based sorbents (hydrated limes and silicate compounds) were investigated. A number of oxidizing additives at different concentrations were used in the Ca-based sorbent production process. The Hg0, SO2, and NOx capture capacities of these oxidant-enriched sorbents were evaluated and compared to those of a commercially available activated carbon in bench-scale, fixed-bed, and fluid-bed systems. Calcium-based sorbents prepared with two oxidants, designated C and M, exhibited Hg0 sorption capacities (approximately 100 microg/g) comparable to that of the activated carbon; they showed far superior SO2 and NOx sorption capacities. Preliminary cost estimates for the process utilizing these novel sorbents indicate potential for substantial lowering of control costs, as compared with other processes currently used or considered for control of Hg0, SO2, and NOx emissions from coal-fired boilers. The implications of these findings toward development of multipollutant control technologies and planned pilot and field evaluations of more promising multipollutant sorbents are summarily discussed.