城市生活垃圾焚烧过程中二次污染物的生成与控制

在我国，采用焚烧法处理城市固体垃圾，逐渐得到推广和应用，然而焚烧带来的二次污染物，如二恶Ying，细颗粒，重金属，HCl以及SOx,NOx等也随之引起了广泛关注，对垃圾焚烧过程中各种二次污染物的产生机理及其控制方法进行了综述。并且指出近期我国城市固体垃圾焚烧烟气污染物的重点控制对象应为颗粒物，HCl,SOx和NOx。     

新型转式垃圾焚烧炉焚烧技术研究

研究了新型转式焚烧炉稳定燃烧工艺和有机垃圾在新型转式焚烧炉中焚烧过程HCl和NOx释放和控制特性。结果表明,新型转式焚烧炉采用二次燃烧技术,能有效控制和降低二次污染物的生成。     

低污染的危险废物焚烧技术研究

目前危险废物焚烧中产生的污染物主要通过尾气处理去除 ,本文认为尾气处理应与通过控制焚烧条件减少尾气中污染物的原始浓度相结合 ,以减少后续处理设备的投资。本文主要讨论了控制危险废物焚烧中主要污染物颗粒物、氯化氢、SOx、NOx、二的焚烧技术     

低污染的危险废物焚烧技术研究

目前危险废物焚烧中产生的污染主要通过尾气处理去除,本文认为尾气处理应与通过控制焚烧条件减少尾气中污染物的原始浓度相结合,以减少后续处理设备的投资。本文主要讨论了控制危险废物焚烧中主要污染物颗粒物、氯化氢、SOx、NOx、二恶英的焚烧技术。     

O3氧化结合化学吸收同时脱硫脱硝的动力学及热力学研究

构建了O3氧化多种污染物的反应机制,并对O3氧化SOx、NOx过程进行动力学模拟,然后利用热力学原理计算出Ca(OH)2和CaCO3湿法烟气同时脱硫脱硝吸收反应达到平衡时SOx和NOx的分压力.结果表明,Ca(OH)2作吸收剂湿法烟气同时脱硫脱硝比CaCO3作吸收剂效果好,而且两者几乎100％地去除烟气中的SOx和NO...     

垃圾焚烧发电过程中的二次污染物控制处理技术

概述了二口恶英、重金属、酸性气体、灰渣等垃圾焚烧二次污染物的形成机理，并详细介绍了通过控制垃圾焚烧条件、尾气处理以及吸附等方法，可以有效控制二口恶英类污染物的排放；重金属的控制可以用除尘器或使用相应的吸附剂处理；采用较为成熟的烟气处理技术，可以控制处理酸性气体；灰渣可采用固化稳定化和酸或其他溶剂提出法处置。     

我国垃圾焚烧处理现状及其发展

本文对我国垃圾焚烧处理的现状和发展趋势进行了综述。垃圾焚烧处理符合资源化、减量化和无害化的原则,由于经济技术水平的限制,我国城市垃圾的处理主要是以填埋和堆肥为主,焚烧法处理占的比例较少,随着经济技术水平的提高,焚烧处理垃圾将得到迅速的发展。我国垃圾焚烧处理的发展应积极的引进、吸收、消化国外的先进技术,开发生产适合我国国情的垃圾焚烧设备;加强法规建设,实现垃圾焚烧处理的规范化管理;开发废气净化设备及其二次污染控制设备;确保焚烧废气达标排放;有效的对垃圾焚烧排放污染物的监控,保证垃圾焚烧处理设施安全、高效的运行。     

二氧化钛脱除高温烟气中的氯化氢

HCl是城市垃圾焚烧产生的主要气体污染物之一。将一种新型脱氯剂TiO2引入到垃圾焚烧系统中,并与其他脱氯剂的性能进行比较。研究了不同脱氯剂使用量、不同反应温度和不同HCl气体浓度对TiO2、CaO和CaTiO3脱氯效果的影响。结果显示,TiO2能在高温(800~1 000℃)、高HCl浓度(1 303.6~1 629.5 mg/m3)下获得较好的脱氯效果。与传统的脱氯剂CaO相比,TiO2更适合于高温烟气脱氯,其在1 000℃时的氯容(36.3 mg HCl/g TiO2)几乎是相同情况下的CaO氯容(9.3 mg HCl/g CaO)的4倍。而CaTiO3的脱氯效果不但受到自身分解效率的影响,还受到TiO2和CaO脱氯效果的影响,其脱氯效果较差。     

垃圾分类背景下厨余垃圾剔除比例对生活垃圾焚烧厂NOx排放的影响

收集了生活垃圾焚烧厂关停SNCR时燃料的N排放数据以及与之对应的工况和燃料特性数据,并分析各影响因素对燃料N转化过程中不同环节的影响机理.结果表明,在工业化生产中,燃料N转化率与炉温、垃圾含水率之间不存在显著联系,而随N元素含量和固定碳含量的增加而降低,随过剩空气系数、H/N、O/N的增加而升高.据此提出了符合实际生产条件的燃料N转化路径图.该路径图表明,燃料特性对燃料N转化率和NOx生成浓度起到了决定性作用,并进一步量化了H/N和固定碳含量这2个参数与燃料N转化率之间的关系.提出通过将厨余垃圾从生活垃圾分出的方法来减少NOx生成,并以国内典型城市为例,研究了分出不同比例厨余垃圾的情况下,燃料N转化率和NOx生成浓度的变化趋势.本研究表明通过分出厨余垃圾的方法,能够降低垃圾焚烧厂的脱硝成本及氨逃逸风险,可为进一步控制生活垃圾焚烧过程中的NOx排放提供参考.     

150t/d循环流化床生活垃圾焚烧炉的工艺结构与污染排放

垃圾焚烧处理技术在我国的应用越来越广泛 ,单纯引进国外的垃圾焚烧处理技术已经无法满足我国经济发展的需要。清华大学自主开发研制的 15 0t/d循环流化床生活垃圾焚烧炉已经通过专家鉴定 ,各项焚烧污染物排放指标均达到或优于国家标准 ,总体水平居国内领先水平。本文详细介绍了该焚烧炉的系统及结构 ,并对有关控制污染物排放的技术手段进行了详细分析     

锅炉烟气联合脱硫脱氮技术

硫氧化物和氮氧化物是燃煤锅炉排放的主要污染物 ,传统分步脱硫脱氮设备昂贵且效率不高 ,而联合脱硫脱氮技术具有很大的优越性 ,如可以减小系统的复杂性、具有更好的运行性能、较低的成本及较小的占地面积 ,因此实现在一个系统内同时脱硫脱氮的工艺成为国内外烟气净化技术的研究重点。对近年来国内外各种联合脱硫脱氮技术的脱除原理、研究现状、应用情况和主要优缺点进行了论述 ,并对各工艺的经济技术指标给予了多方面的比较。通过对两类烟气联合脱硫脱氮技术 (炉内联合脱除和烟气中联合脱除 )的分析、综合和比较 ,找出了我国今后脱硫脱氮技术的研究重点 ,从而为脱硫脱氮技术的进一步开发和改进提供参考     

The utilization of catalyst sorbent in scrubbing acid gases from incineration flue gas

Catalyst sorbents based on alumina-supported CuO, CeO2, and CuO-CeO2 were applied to a dry scrubber to clean up the SO2/HCl/NO simultaneously from pilot-scale fluidized-bed incineration flue gas. In the presence of organic compounds, CO and the submicron particles SO2 and HCI removed by the fresh catalyst sorbents and NO reduced to N2 by NH3 under the catalysis of fresh and spent desulfurization/dechloridization (DeSO2/DeHCl) catalyst sorbents (copper compounds, Cu, CuO, and CuSO4) were evaluated in this paper. The fresh and spent catalyst sorbents were characterized by the Brunner-Emmett-Teller method (BET), X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), inductively coupled plasma-mass spectrometry (ICP-MS), and the elemental analyzer (EA). The study showed that the performances of CuO, CeO2, and CuO-CeO2/gamma-Al2O3 were better than that of Ca(OH)2. The removal efficiency of SO2 and HCl was 80-95% in the dry scrubber system. Under NH3/NO = 1, NO could not be reduced to N2 because it was difficult to control the ratio of air/fuel in the flue gas. For estimating the feasibility of regenerating the spent catalyst sorbents, BET and EA analyses were used. They indicated that the pore structures were nearly maintained and a small amount of carbon accumulated on their surface.     

Economics of an integrated approach to control SO2, NOX,HCl, and particulate emissions from power plants

An integrated approach for the simultaneous reduction of major combustion-generated pollutants from power plants is presented along with a simplified economic analysis. With this technology, the synergistic effects of high-temperature sorbent/coal or sorbent/natural gas injection and high-temperature flue gas filtration are exploited. Calcium-based (or Na-based, etc.) sorbents are sprayed in the post-flame zone of a furnace, where they react with S- and Cl-containing gases to form stable salts of Ca (or Na, etc.). The partially reacted sorbent is then collected in a high-temperature ceramic filter, which is placed downstream of the sorbent injection point, where it further reacts for a prolonged period of time. With this technique, both the likelihood of contact and the length of time of contact between the solid sorbent particles and the gaseous pollutants increase, because reaction takes place both in the furnace upstream of the filter and inside the filter itself. Hence, the sorbent utilization increases significantly. Several pollutants, such as SO2, H2S, HCl, and particulate (soot, ash, and tar), may be partially removed from the effluent. The organic content of the sorbents (or blends) also pyrolyzes and reduces NOx. Unburned carbon in the ash may be completely oxidized in the filter. The filter is cleaned periodically with aerodynamic regeneration (back pulsing) without interrupting furnace operation. The effectiveness of this technique has been shown in laboratory-scale experiments using either rather costly carboxylic salts of Ca or low- to moderate-cost blends of limestone, lime, or sodium bicarbonate with coal fines. Injection occurred in the furnace at 1150 degrees C, while the filter was maintained at 600 degrees C. Results showed that 65 or 40% SO2 removal was obtained with calcium formate or a limestone/coal blend, respectively, at an entering calcium-to-sulfur molar ratio of 2. A sodium bicarbonate/coal blend resulted in 78% SO2 removal at a sodium-to-sulfur molar ratio of 2. HCl removal efficiencies have been shown to be higher than those for SO2. NOx reductions of 40% have been observed with a fuel (coal)-to-air equivalence ratio, phi, around 2. The filter has been shown to be 97-99% efficient in removing PM2.5 particulates. Calculations herein show that this integrated sorbent/filter method is cost-effective, in comparison with current technologies, on both capital cost ($/kW) and levelized cost ($/ton pollutant removed) bases, if a limestone/coal mixture is used as the sorbent for fossil fuel plants. Capital costs for the filter/sorbent combination are estimated to be in the range of $61-$105/kW for a new plant. Because current technologies are designed for removing one pollutant at a time, both their cost and space requirements are higher than those of this integrated technique. At the minimum projected removal efficiencies for HCl/SO2/NOx of about 40%, the levelized costs are projected to be $203-$261/ton of combined pollutant SO2/HCl/NOx and particulates removed from coal-fired power plants.     

The importance of the location of sodium chlorite application in a multipollutant flue gas cleaning system

In this study, removing sulfur dioxide (SO2), nitrogen oxides (NO(x)), and mercury (Hg) from simulated flue gas was investigated in two laboratory-sized bubbling reactors that simulated an oxidizing reactor (where the NO and Hg(0) oxidation reactions are expected to occur) and a wet limestone scrubber, respectively. A sodium chlorite solution was used as the oxidizing agent. The sodium chlorite solution was an effective additive that enhanced the NO(x), Hg, and SO2 capture from the flue gas. Furthermore, it was discovered that the location of the sodium chlorite application (before, in, or after the wet scrubber) greatly influences which pollutants are removed and the amount removed. This effect is related to the chemical conditions (pH, absence/presence of particular gases) that are present at different positions throughout the flue gas cleaning system profile. The research results indicated that there is a potential to achieve nearly zero SO2, NO(x), and Hg emissions (complete SO2, NO, and Hg removals and -90% of NO(x) absorption from initial values of 1500 ppmv of SO2, 200 ppmv of NO(x), and 206 microg/m3 of Hg(0)) from the flue gas when sodium chlorite was applied before the wet limestone scrubber. However applying the oxidizer after the wet limestone scrubber was the most effective configuration for Hg and NO(x) control for extremely low chlorite concentrations (below 0.002 M) and therefore appears to be the best configuration for Hg control or as an additional step in NO(x) recleaning (after other NO(x) control facilities). The multipollutant scrubber, into which the chlorite was injected simultaneously with the calcium carbonate slurry, appeared to be the least expensive solution (when consider only capital cost), but exhibited the lowest NO(x) absorption at -50%. The bench-scale test results presented can be used to develop performance predictions for a full- or pilot-scale multipollutant flue gas cleaning system equipped with wet flue gas desulfurization scrubber.     

Application of fluidized bed combustion to industrial waste treatment

Landfill and sea-dumping appear to be on their way out as acceptable methods for the disposal of untreated industrial wastes in Taiwan. Recently, there has been interest in the application of fluidized bed technology to waste incineration for efficient energy utilization and environmental protection. A pilot fluidized bed combustion system was used to investigate the incineration performance and parametric test for the waste from an industrial park. According to the experimental results, the appropriate operating conditions, including temperatures of 800-840 degrees C, aeration rates of U(0)/Um(f)-2.0 or so, and on-bed feeding, were recommended to treat such waste. The emissions of SO(x), NO(x) and CO in flue gas meet the ROC-EPA regulation.     

Atmospheric deposition inputs and effects on lichen chemistry and indicator species in the Columbia River Gorge, USA

Topographic and meteorological conditions make the Columbia River Gorge (CRG) an 'exhaust pipe' for air pollutants generated by the Portland-Vancouver metropolis and Columbia Basin. We sampled fog, bulk precipitation, throughfall, airborne particulates, lichen thalli, and nitrophytic lichen distribution. Throughfall N and S deposition were high, 11.5-25.4 and 3.4-6.7 kg ha(-1) over 4.5 months at all 9 and 4/9 sites, respectively. Deposition and lichen thallus N were highest at eastern- and western-most sites, implicating both agricultural and urban sources. Fog and precipitation pH were frequently as low as 3.7-5.0. Peak NO(x), NH(3), and SO(2) concentrations in the eastern CRG were low, suggesting enhanced N and S inputs were largely from particulate deposition. Lichens indicating nitrogen-enriched environments were abundant and lichen N and S concentrations were 2x higher in the CRG than surrounding national forests. The atmospheric deposition levels detected likely threaten Gorge ecosystems and cultural resources.     

The need for ammonia abatement with respect to secondary PM reductions in Europe

In Europe, secondary particulate matter (PM) comprises 50% or more of PM 2.5. To reduce PM concentrations requires lowering precursor emissions. Since the 1980s, SO(2) emissions have decreased by more than 60%, while particle concentrations have decreased less. NO(x) and NH(3) emissions have decreased slightly. The role of ammonia in particle formation is addressed here. It is shown that secondary PM concentrations can only be effectively reduced if ammonia emissions are decreased in much the same way as those of SO(2) and NO(x).     

Seasonal variation of air pollution index: Hong Kong case study

Air pollution is an important and popular topic in Hong Kong as concerns have been raised about the health impacts caused by vehicle exhausts in recent years. In Hong Kong, sulphur dioxide SO2, nitrogen dioxide (NO2), nitric oxide (NO), carbon monoxide (CO), and respirable suspended particulates (RSP) are major air pollutants caused by the dominant usage of diesel fuel by goods vehicles and buses. These major pollutants and the related secondary pollutant, e.g., ozone (O3), become and impose harmful impact on human health in Hong Kong area after the northern shifting of major industries to Mainland China. The air pollution index (API), a referential parameter describing air pollution levels, provides information to enhance the public awareness of air pollutions in time series since 1995. In this study, the varying trends of API and the levels of related air pollutants are analyzed based on the database monitored at a selected roadside air quality monitoring station, i.e., Causeway Bay, during 1999-2003. Firstly, the original measured pollutant data and the resultant APIs are analyzed statistically in different time series including daily, monthly, seasonal patterns. It is found that the daily mean APIs in seasonal period can be regarded as stationary time series. Secondly, the auto-regressive moving average (ARMA) method, implemented by Box-Jenkins model, is used to forecast the API time series in different seasonal specifications. The performance evaluations of the adopted models are also carried out and discussed according to Bayesian information criteria (BIC) and root mean square error (RMSE). The results indicate that the ARMA model can provide reliable, satisfactory predictions for the problem interested and is expecting to be an alternative tool for practical assessment and justification.     

Characterization of atmospheric PM10 and related chemical species in southern Taiwan during the episode days

The concentrations of atmospheric PM10 on days with episodes of pollution were examined at four different sampling sites (CC, DL, LY, and HK) in southern Taiwan. The related to particulates water-soluble ionic species (Na+, K+, Mg2+, Ca2+, NH4+, Cl-, NO3-, SO4(2-)), carbonaceous species (EC and OC) and metallic species (Zn, Ni, Pb, Fe, Mn, Al, Si, V) were also analyzed. On the episode days of this study, the PM10 mass concentration ranged from 155 to 210 microgm(-3), from 150 to 208 microgm(-3), from 182 to 249 microgm(-3), and from 166 to 228 microgm(-3) at CC, DL, LY, and HK, respectively. The results indicate that the dominant water-soluble species were SO4(2-), NO3-, NH4+, and Cl- at the four sampling sites on these days. Moreover, the high sulfate and nitrate conversion values (SOR and NOR) presented herein suggest that secondary formations from SO2 to SO4(2-) and from NO2 to NO3- are present in significant quantities in the atmosphere of southern Taiwan on episode days. In particular, high SOR and NOR verified that both SO4(2-) and NO3- dominated the increase of atmospheric PM10 concentration in southern Taiwan on episode days.     

Chemical composition and source apportionment of PM2.5 particles in the Sihwa area, Korea

To investigate the chemical characteristics of fine particles in the Sihwa area, Korea, atmospheric aerosol samples were collected using a dichotomous PM10 sampler and two URG PM2.5 cyclone samplers during five intensive sampling periods between February 1998 and February 1999. The Inductively Coupled Plasma (ICP)-Atomic Emission Spectrometry (AES)/ICP-Mass Spectrometry (MS), ion chromatograph (IC), and thermal manganese dioxide oxidation (TMO) methods were used to analyze the trace elements, ionic species, and carbonaceous species, respectively. Backward trajectory analysis, factor analysis, and a chemical mass balance (CMB) model were used to estimate quantitatively source contributions to PM2.5 particles collected in the Sihwa area. The results of PM2.5 source apportionment using the CMB7 receptor model showed that (NH4)2SO4 was, on average, the major contributor to PM2.5 particles, followed by nontraffic organic carbon (OC) emission, NH4NO3, agricultural waste burning, motor vehicle emission, road dust, waste incineration, marine aerosol, and others. Here, the nontraffic OC sources include primary anthropogenic OC emitted from the industrial complex zone, secondary OC, and organic species from distant sources. The source impact of waste incineration emission became significant when the dominant wind directions were from southwest and west sectors during the sampling periods. It was found that PM2.5 particles in the Sihwa area were influenced mainly by both anthropogenic local sources and long-range transport and transformation of air pollutants.