Acidifying emissions in The Netherlands

The emission of acidifying compounds to air in the Netherlands, expressed as acidifying equivalents, consisted in 1992 mainly of NO_X (45%), NH₃ (35%) and SO₂ (20%). Transportation, agriculture and large combustion plants each contributed about 30% to the national total emission of acidifying compounds. The emissions from transportation activities mainly consisted of NO_X, while in agriculture NH₃ emission strongly dominated. Combustion processes in large combustion plants resulted both in SO₂ emissions (especially from refineries) and NO_X emissions (especially from public power plants). The total emission of acidifying substances decreases steadily in the Netherlands. The emission in 1992 was 24% lower than in 1985. It is expected to decrease further in future. The emission levels in 1992 and 1993 still are more than twice as high as the emission objective for the year 2000, set by Dutch environmental policy.     

Estimation of source-receptor matrices for deposition of NOx-N

The contributions of the anthropogenic sources of NO_x from various combinations of contiguous U.S. states or Canadian provinces to integrated deposition across selected states or provinces are estimated with the Advanced Statistical Trajectory Regional Air Pollution (ASTRAP) model. The model assumes linearity between emissions and deposition, and uses the same parameterization methods, although with different rates, as in simulations of transport and deposition of SO_X. Vertical distributions of emissions for the two classes of pollutants are substantially different in the gridded inventories used in simulations, with a weighted mean effective emission height of 160 m for NO_X and 310 m for SO_X. This might be expected to lead to an effective transport distance before deposition shorter for NO_X than for SO_X. However, the calculated fraction of NO_X emissions deposited within the contiguous United States and Canada south of 60 deg N (57%) is not greatly different from the fraction calculated for SOX emissions (54%). This suggests that there may be compensating factors in the horizontal distribution of NO_X emissions, and in the lower dry deposition velocities for NO/NO₂ than for SO₂ in ASTRAP.     

Characterization of Cement Plant Emissions in Turkey

In cement plants in Turkey CO, NO₂, SO₂ and particulate emissions were measured using standard measurement techniques and equipment. Emission factors are calculated by dividing the emission rates by capacity of production at the time of measurements for each plant. The results of this study show that the dominant emissions from cement production in Turkey is CO followed by NO₂, dust and SO₂ in decreasing order. National averages for the emission factors are calculated and compared to international emission factors. On average the Turkish dust emission factor is higher than the German factor, however NO₂ and SO₂ emission factors are lower in Turkey.     

European emission data with high temporal and spatial resolution

The estimation of acidic deposition strongly depends on the availability of accurate emission data. The atmospheric models, that calculate concentrations and depositions of pollutants, need data in a high temporal resolution (e.g. daily, 6-hourly or even hourly data). However, although some progress has been achieved concerning annual emission data for Europe (e.g. CORINAIR 90), only very little information is available about the temporal variation of these emissions during a year. Therefore, within the EUROTRAC-GENEMIS project special emphasis was laid on the development of methods to generate emissions with a high temporal and spatial resolution. As results the temporal and spatial distribution of SO₂- and NO_X-emissions are shown. The results indicate, that the emissions vary considerably over time and that the use of simple patterns for the temporal disaggregation is not sufficient for modelling and assessment of acidic deposition.     

Control techniques and strategies for regional air pollution control from energy and industrial sectors

The technological options currently available to reduce SO₂ and NO_x emissions including abatement technologies and high efficient energy conversion technologies are reviewed. The energy emission model EFOMENV (Energy Flow Optimization Model-Environment) which takes into account all relevant emission reduction measures is used to determine the cost optimized energy pathway, the ranking of reduction measures and the corresponding costs as a function of given reduction levels of SO₂ and/or NO_x emissions for different scenarios in selected Central and Eastern European countries. It is shown that restructuring of the energy system is a major emission reduction option in all countries but with a potential varying greatly from country to country depending mainly on the existing structure and the age of the plants and on the development of the energy demand. The emission reduction costs for SO₂ in Central and Eastern European countries are 50% to 70% lower than in Western countries due to high potential of fuel/technology switching and energy saving measures. Cost efficient measures to reduce CO₂ emissions also lead to a significant decrease of SO₂ and NO_x emissions.     

Emission Inventories,Emission Control Options and Control Strategies: An Overview of Recent Developments

Accurate emission inventories are crucial for informed decisions about emission control strategies. Emission inventory activities are now well established throughout the world and a large body of resources is available to assist in estimating emissions at the global, regional and local scale. Work is ongoing to refine methodologies and to address additional sources and pollutants such as fine particulate matter. During the last decade innovative concepts for emission control legislation were developed. Market based instruments can achieve envisaged emission reductions at lower costs than conventional approaches. Air quality management is now understood as a multi-pollutant, multi-effect task, which offers a significant cost saving potential if synergistic effects are fully utilized. Integrated assessment models proved useful in managing the vast volume of relevant information needed for the design of cost-effective emission control strategies. Europe and North America have embarked on ambitious control strategies that will lead to significant reductions in the emissions of some of the conventional pollutants (e.g., SO₂, NO_x, VOC). There are also first indications of a structural break that could reverse the long-term growth trend of SO₂ emissions also in the fast developing nations of Asia.     

Cost-Effective Abatement of Acidifying Emissions with Flue Gas Cleaning vs. Fuel Switching in Finland

Acidifying emissions from energy production and industry have decreased considerably during the last two decades in Finland. Especially the emissions of sulphur dioxide have dropped sharply with 85% in 1980–1998, although the energy use has increased 30% during the same period. The reduction has occurred through two mechanisms: by replacing the combustion of heavy fuel oil with cleaner energy carriers, and by direct emission reduction controls, e.g. flue gas desulphurization. In this study the Finnish cost curves for SO₂ and NO_x were first calculated to produce a consistent comprehensive view on further emission reduction costs and potentials. The data on technical and cost-related parameters were based on actual national experiences from power plants and industry. Most of the cost-efficient sulphur emission controls were already in use. For NO_x, a large share of further reduction potential still remained. Second, a case on the emission reductions and costs for fuel switching in a 205 MW_th peat power plant of Tampere Power Utility in Finland was studied. Fuel switching to natural gas was found less cost-efficient in SO₂ and NO_x emission reduction when compared to flue gas cleaning techniques. The findings provided new information on fuel switching as an alternative potential reduction measure, which is not considered in international assessments.     

Projections of SO2, NOx,NH3 and VOC Emissions in East Asia Up to 2030

Starting from an inventory of SO₂, NO_x, VOC and NH₃ emissions for the years 1990 and 1995 in East Asia (Japan, South and North Korea, China, Mongolia and Taiwan), the temporal development of the emissions of the four air pollutants is projected to the year 2030 based on scenarios of economic development. The projections are prepared at a regional level (prefectures or provinces of individual countries) and distinguish more than 100 source categories for each region. The emission estimates are presented with a spatial resolution of 1×1 degree longitude/latitude. First results suggest that, due to the emission control legislation taken in the region, SO₂ emissions would only grow by about 46 percent until 2030. Emissions of NO_x and VOC may increase by 95 and 65 percent, respectively, mainly driven by the expected increase in road traffic volume. Ammonia, mainly emitted from agriculture, is projected to double by 2030.     

A Computational Approach Based on GIS Technology for the Development of an Anthropogenic Emission Inventory of Gaseous Pollutants in Greece

This paper describes a computational system developed for the compilation of an anthropogenic emission inventory of gaseous pollutants for Greece. The inventory was developed using a geographical information system integrated with SQL programming language to provide high temporal gridded emission fields for CO, NO₂, NO, SO₂, NH₃ and 23 non-methane volatile organic compounds (NMVOCs) species for the reference year 2003. Activity and statistical data from national sources were used for the quantification of emissions from the road transport, the other mobile sources and machinery sectors and from range activities using top-down or bottom-up methodologies. Annual emission data from existing national and European emission databases were also used. The emission data were spatially and temporally disaggregated using source-specific spatiotemporal indicators. On national scale, the road transport sector produces about 60% of the annual CO and NMVOC total emissions, with gasoline vehicles being the main CO and NMVOC emissions source. The road transport is responsible for approximately half of the higher alkanes and for more than half of the ethene and toluene emissions. The maritime sector accounts for about 40% of the annual total NO_x emissions, most of which are emitted by the international shipping subsector, whilst SO₂ is emitted mainly by the energy sector. The evaluation of the emissions inventory suggests that it provides a good representation of the amounts of gaseous pollutants emitted on national scale and a good characterisation of the relative composition of CO and NO_x emission in the large urban centres.     

Development of a Multi-Resolution Emission Inventory and Its Impact on Sulfur Distribution for Northeast Asia

Emissions in East Asia for 1993 by administrative units and source types are estimated to support regional emission assessments and transport modeling studies. Total emission of SO_x, NO_x, soil NO_x, N₂O, and NH₃ are 24 150, 12 610, 1963, 908, and 8263 kton yr^-1, respectively.China's emission contribution is the highest for every species.The area sources are the most significant source type for SO_x and NO_x, but the fraction due to mobile source is highest for NO_x. Major LPSs are located from the middle to the east part of China, south and middle-west part of South Korea, and the east part of Japan. The area sources of SO_x show a pattern similar to population density, whereas NH₃ shows a strong landuse dependency. Detail emissions analysis reveals higher SO_x emission `cores' within each province. The estimated emissions are used to estimate sulfur deposition in the regions. The seasonal average sulfur distribution amounts are estimated from the ATMOS2 chemical transport model. The results showed anti-correlation with temperature for sulfur (SO₂ + SO₄ ^-2) concentrations and a positive correlation with rainfall for deposition.     

土壤氮氧化物排放及其对中国地区对流层光化学特性影响的数值模拟研究

利用Williams的模型估计中国地区土壤氮氧化物(NOX,包括NO和NO2)的排放,并运用中尺度气象模式MM5以及光化学模式Calgrid模拟不同季节和不同人为源情况下土壤NOX排放对中国地区光化学的影响。模拟结果表明,中国地区土壤NOX排放总量为225.8 Gg N,是人为源的7%,这一比例在夏季将达到23.4%;排放量有明显季节变化和空间变化。土壤源不仅使NOX、O3、HNO3和过氧乙酰硝酸酯(PeroxyacetylNitrate,PAN)的全国平均浓度增加,还显著改变了污染物的空间分布。4种污染物全国平均浓度的最大增量分别为2.37、26.08、9.79和0.43μg m-3,增量在夏季明显高于其他季节,在各地区的增减随排放源、气象条件和光化学特性的不同而不同。随着人为NOX排放的增加,土壤源在光化学中的作用会更加显著。土壤NOX排放在对流层光化学过程中的作用不容忽视。     

An Integrated Assessment Model for Fine Particulate Matter in Europe

Exposure to fine particles in the ambient air is recognized as a significant threat to human health. Two pathways contribute to the particle burden in the atmosphere: Fine particles originate from primary emissions, and secondary organic and inorganic particles are formed from the gas phase from the emissions of 'conventional' pollutants such as SO₂, NO_x, VOC and NH₃. Both types of particulate matter can be transported over long distances in the atmosphere. An integrated assessment model for particulate matter developed at IIASA addresses the relative importance of the different types of particulates, distinguishing primary and secondary particles and two size fractions. The model projects these emissions into the future and seeks cost-effective strategies for reducing health risks to population. The model integrates the control of primary emissions of fine particles with strategies to reduce the precursor emissions for the secondary aerosols. Preliminary results addressing the PM_2.5 fraction of both primary and secondary particulate matter indicate that in Europe the exposure to particulates will be significantly reduced as a side effect of the emission controls for conventional air pollutants (SO₂, NO_x, NH₃).     

The role of nitrogen oxides in oxidant production as predicted by the Regional Acid Deposition Model (RADM)

Regional oxidant distributions produced under various atmospheric conditions and emission scenarios are investigated using the Regional Acid Deposition Model (RADM). RADM is a complex, evolving three-dimensional Eulerian model that describes the chemistry, transport and deposition of tropospheric trace species including SO₂, sulfate, NO _x and volatile organic compounds as well as O₃, other major oxidants and acids. The model calculates the short-term temporal evolution of atmospheric trace gas concentrations and their deposition on the regional scale. This study is focused on oxidant production in the eastern United States and southeastern Canada. The influence of atmospheric conditions is explored by comparing three characteristic winter, summer and spring/fall cases. Base-case 1985 emissions of SO _x , NO _x , volatile organic compounds (VOCs), NH₃ and CO are specified using the comprehensive pollutant emissions inventory developed as part of the National Acid Precipitation Assessment Program (NAPAP). The perturbed case, which represents projected anthropogenic emission changes for 2010, indicates changes in daily total 80 km grid average NO _x emissions ranging from increases of 75% to decreases of 45% and VOC emission changes ranging from increases of 65% to decreases of 20%. The largest NO _x emission changes occur in the northeast, and the largest VOC changes occur in the Gulf Coast area. Ground level grid average midday O₃ concentrations for the 1985 emission cases are highest (on the order of 70 to 100 ppb) in the New York City and Houston metropolitan areas for the summer and spring cases; the summer case also indicates relatively high grid average O₃ concentrations of greater than 80 ppb in the southeast. Winter case values are much lower than summer O₃ values throughout the region, with highs of 40 to 50 ppb occurring in the southeast and the Great Lakes area. Changes in NO _x and other emissions under the complex 2010 emissions scenario for the summer case result in maximum O₃ concentration reductions of 10% in the Houston area and increases in O₃ of a few percent in some rural areas of the southeast. This study underscores the need for more comprehensive assessment of the complex relationships among regional emission changes, oxidant production and atmospheric conditions.     

Methodology and Results of the REKLIP Atmospheric Emission Inventory of the Upper Rhine Valley Transborder Region

In the frame of the climatological project REKLIPwhich involves part of Switzerland, Germany and Franceand concerns the upper Rhine valley, an atmosphericemission inventory has been established with a spatialresolution of a square kilometer and a time resolutionup to one hour. Anthropogenic emissions of SO₂, NO_x,CO, HCl and volatile organic compounds (VOC) divided into thirty compounds or group of compounds as well as biogenic emissions of NMVOC have been taken into account for the year 1990. This inventory has been updated for the following years until 1993 and some hourly emissions inventories have been derived for a period of several days of September 1992,corresponding to a REKLIP intensive measurement campaign.     

Precipitation Composition in the Ohio River Valley: Spatial Variability and Temporal Trends

Sulfate (SO₄ ^2?), nitrate (NO₃ ^?) and ammonium (NH₄ ⁺) concentrations in precipitation as measured at NADP sites within the Ohio River Valley of the Midwestern USA between 1985 and 2002 are quantified and temporal trends attributed to changes/ variations in (i) the precipitation regime, (ii) emission patterns and (iii) air mass trajectories. The results indicate that mean SO₄ ^2? concentrations in precipitation declined by 37–43% between 1985 and 2002, while NO₃ ^? concentrations decreased by 1–32%, and NH₄ ⁺ concentrations exhibited declining concentrations at some sites and increasing concentrations at others. The change in SO₄ ^2? concentrations is in broad agreement with estimated reductions in sulfur dioxide emissions. Changes in NO₃ ^? concentrations appear to be less closely related to variations in emissions of oxides of nitrogen and exhibit a stronger dependence on weekly precipitation volume. Up to one quarter of the variability in log-transformed weekly NO₃ ^? concentrations in precipitation is explicable by variations in precipitation volume. Trends in annual average log-transformed SO₄ ^2? concentrations exhibit only a relatively small influence of variability in weekly precipitation amount but at each of the sites considered the variance explanation of annual average log-transformed SO₄ ^2? by sampling year was increased by removing the influence of precipitation volume. Annual mean log-transformed ion concentrations detrended for precipitation volume (by week) and emission changes (by year) exhibit positive correlations at all sites, indicating that the residual variability of SO₄ ^2?, NO₃ ^? and NH₄ ⁺ may have a common source which is postulated to be linked to synoptic scale variability and air mass trajectories.     

Long-Term Changes of Particulate Emission in the Industrial Region of Upper Silesia (Poland) and their Effect on the Acidity of Rainwater

The article presents data from ten-year measurements, which provethat the positive effects in particulate emission were accompanied by some adverse effects in the form of acidified rainwater. A distinctive change of rainwater pH in the SilesiaRegion (Poland) was first recorded in the early 90's. While in 1989, pH of over 55% of the investigated rainwater samples wasabove 6, in 1997 the average yearly pH was 4.1 and the pH of20%of the investigated samples was in the range of 3.1–4.0. Seekingthe reason for an increased acidity of rainwater, pH values were compared with emission changes of particulate, SO₂ and NO₂ acrossthe studied area. Emission factors of Ca, Mg, Na and K were determined based on the data of particulate matter emission fromcement production processes, coal combustion processes and metallurgy. This allowed comparing the changes of pH rainwater with the area emissions of alkali elements. An analysis of thecorrelation between pH values and the changes of particulatematter and alkali elements emission as well as SO₂ and NO₂ emission in the area under study showed that particulate emission followed by SO₂ emission had the strongest impact onthe modification of rainwater pH, while the impact of NO₂ emission was less distinctive. Additionally, an analysis was made to investigate the relationbetween rainwater pH and the concentration of alkaline ions inrainwater samples. The highest value r = 0.96 was recorded forMg²⁺ ions, the lowest i.e. r = 0.54 for Ca²⁺ ions.This situation can be explained by the fact that calciumcompounds are the soluble substances among the investigatedmetals. Thus, despite the presence of calcium compounds inrainwater samples, a large amount of their portion does notinfluence rainwater pH.     

Trends in Emissions of Acidifying Species in Asia, 1985–1997

Acid deposition is a serious problem throughout much of Asia. Emissions of sulfur dioxide (SO₂) and nitrogen oxides (NO_x) have been increasing steadily, as nations strive to increase their levels of economic development. Coal and fuel oil have been the main choices for powering industrial development; and, until recently, only a few countries had taken steps to avert the atmospheric emissions that accompany fuel combustion. This paper discusses trends in emissions of SO₂ and NO_x that have occurred in Asian countries in the period 1985–1997, using results from the RAINS-Asia computer model and energy-use trends from the IEA Energy Statistics and Balances database. Emissions of SO₂ in Asia grew from 26.6 Tg in 1985 to 33.7 Tg in 1990 and 39.2 Tg in 1997. Though SO₂ emissions used to grow as fast as fossil-fuel use, recent limitations on the sulfur content of coal and oil have slowed the growth. The annual-average emissions growth between 1990 and 1997 was only 2.2%, considerably less than the economic growth rate. Emissions of NO_x, on the other hand, continue to grow rapidly, from 14.1 Tg in 1985 to 18.7 Tg in 1990 and 28.5 Tg in 1997 (6.2% per year between 1990 and 1997), with no signs of abating. Thus, though SO₂ remains the major contributor to acidifying emissions in Asia, the role of NO_x will become more and more important in the future.     

Modeling study of SO x and NO x transport during the January 1985 SMOG episode

For the January 1985 smog episode concentrations of SO₂, sulphate (SO₄), NO _x (sum of NO and NO₂) and nitrate (NO₃) have been calculated for north-western Europe by means of an atmospheric transport model. The unfavorable dispersion conditions (moderate to low wind speeds, a low mixing height and a strong inversion) and a reduced dry deposition over the snow-covered or frozen soil, in combination with increased space heating emissions due to the exceptionally cold weather, gave rise to high ground level concentrations. In order to study the effectiveness of control measures during this type of episodes, calculations were made for various emission scenarios. The results were evaluated for four receptor areas, two areas relatively close to the major sources (The Netherlands and the Black Forest) and two more remote areas (Scotland and the SW coast of Sweden, near Gothenburg).     

A Module to Calculate Primary Particulate Matter Emissions and Abatement Measures in Europe

Primary particulate matter is emitted directly into the atmosphere from various anthropogenic and natural sources such as power plants (combustion of fossil fuels) or forest fires. Secondary particles are formed by transformation of SO₂, NO_x, NH₃, and VOC in the atmosphere. They both contribute to ambient particulate matter concentrations, which may have adverse effects on human health. Health hazards are caused by small particulate size, high number of especially fine (< 2.5 µm) and ultra-fine (< 0.1 µm) particles and/or their chemical composition. As part of an integrated assessment model developed at IIASA, a module on primary particulate matter (PM) emissions has been added to the existing SO₂, NO_x, NH₃ and VOC sections. The module considers so far primary emissions of total suspended particles (TSP), PM₁₀ and PM_2.5 from aggregated stationary and mobile sources. A primary PM emission database has been established. Country specific emission factors for stationary sources have been calculated within the module using the ash content of solid fuels.     

Regulatory options under the U.S. Clean Air Act: The federal view

This paper documents the evolution of Environmental Protection Agency (EPA) policy concerning the relative roles that volatile organic compounds (VOCs) and oxides of nitrogen (NO_x) emissions play in ozone nonattainment planning for State implementation plans (SIPs). It further discusses possible new control requirements, including NO_x measures, that may be required as a result of pending Clean Air Act Amendments. In the early 1970's EPA guidance emphasized the use of VOC control measures to attain the ozone (formerly oxidant) ambient air quality standard. Little if any, control requirements applied to NO_x emissions. EPA continued to focus guidance requirements upon the control of VOCs during the planning efforts associated with the 1977 Clean Air Act amendments... 1979 SIPs, 1982 plans for long-term problem areas (extension areas), and other revisions to SIPs. Preliminary air quality modeling work to support these later planning efforts revealed that, in certain cases, there were potential benefits of NO_x control in addition to VOC. With this new insight, EPA's post-1987 policy proposal required states to look at the potential benefits of NO_x controls in areas with a nonmethane organic compound to NO_x ratio of 10∶1 or greater. In Clean Air Act Amendments currently being debated in the House and Senate, there is an uncertainty with regard to the role of NO_x controls. Possibilities under consideration range from the application of reasonably available control technology for 100 ton sources of NO_x to a clean fuel motor vehicle program within 42 months of enactment.