出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2018/03/13 22:22:18」(JST)
窒素酸化物(ちっそさんかぶつ、nitrogen oxides) は窒素の酸化物の総称。
一酸化窒素(NO)、二酸化窒素(NO2)、亜酸化窒素(一酸化二窒素)(N2O)、三酸化二窒素(N2O3)、四酸化二窒素(N2O4)、五酸化二窒素(N2O5)など。化学式の NOx から「ノックス」ともいう。
自然界において窒素酸化物は、雷あるいは土壌中の微生物によって生成される。たとえば微生物が多い土壌に豊富な化学肥料を与えると土壌微生物が分解して窒素酸化物を放出する例が知られている。また、二酸化硫黄(SO2)などの硫黄酸化物(SOx)は、石油や石炭などの化石燃料が燃える際に発生する。日本では高度経済成長の時代に、工場からの煙などに含まれる硫黄酸化物(SOx)による大気汚染が進行し、大きな問題になった。
物質が燃焼するときにも一酸化窒素や二酸化窒素などが発生する。この場合、高温・高圧で燃焼することで本来反応しにくい空気中の窒素と酸素が反応して窒素酸化物になる場合(サーマルNOx)と、燃料由来の窒素化合物から窒素酸化物となる場合(フューエルNOx)がある。たとえば、排気ガスや天然ガスボイラー(家庭用調理ガス器具を含む)などから排出される窒素酸化物は前者が主であり、石炭が燃焼した場合の窒素酸化物はそのほとんどが石炭中の窒素化合物に由来することが知られている。
四酸化二窒素は二酸化窒素と平衡状態にあり、環境中など低圧・低濃度では二酸化窒素側に偏っている。
(各窒素酸化物の生成法は当該記事に詳しい)
大気から陸上に沈着する窒素量は、1890年から1990年の100年間で5倍に増加し21世紀初頭時点では 125 Tg Ny-1(テラグラム窒素毎年)とされており、放出量の80 %が肥料が起源で20 %が燃焼が起源である[1]。
二酸化窒素(NO2)自体は中性で肺から吸収されやすい赤褐色の気体または液体。細胞内では二酸化窒素は強い酸化作用を示して細胞を傷害するので、粘膜の刺激、気管支炎、肺水腫などの原因となる。
一酸化窒素(NO)については、1980年代頃から、その生体内での生理機能について研究が進み、血管拡張作用を持つことなどが明らかにされたほか、この一酸化窒素が神経伝達物質としても作用することが判明した。なお、1998年のノーベル生理学・医学賞は、この一酸化窒素の生理作用の発見に対して贈られている。現在でも、その多様な生理機能について研究が続いている。
NO、NO2を吸入するとメトヘモグロビンが生成する[2]。メトヘモグロビンは、通常のヘモグロビンに配位されている二価(フェロ)の鉄イオンが三価(フェリ)になっているもので、酸素を運ぶことができない[3]。
一酸化二窒素(N2O)は麻酔作用を持つため、吸入麻酔剤として医療現場で使用されている。
NOxの防除技術としては、バーナーや燃焼法の改善によって低NOx化を実現する低NOx燃焼法と,排ガス中からNOxを除去する排煙脱硝法がある[4]。
空気中の窒素に起因するいわゆるサーマルNOxと、燃焼中に含まれる窒素化合物に起因するフューエルNOxがある。双方に有効な方法として、燃焼用空気を二段階に分けて吹き込む二段燃焼法が、ガス燃焼から石炭燃焼に至るまで最も広い範囲で用いられている。
湿式法と乾式法があり、大型燃焼装置では現在乾式法の一つである選択触媒法が主流となっている。煙道部の手前で排ガス中にNH3を吹き込み、下流部に設置された触媒反応器で、NH3によるNOの選択的還元を行わせる。
尿素SCRシステム
JR各社では、ディーゼルカーに搭載されているディーゼルエンジンからの窒素酸化物削減に取り組んでおり、JR東日本のキハE130系、JR四国の1500形などが低排出車である。
窒素酸化物は硫黄酸化物とならび酸性雨(酸性降下物)粒子状物質の原因物質で、硫黄酸化物は脱硫装置により液体の化石燃料由来の発生抑制させる事が可能であるが、燃焼(高温との接触)で生成される窒素酸化物の生成抑制は困難である。生成された窒素酸化物は降雨や霧(湿性沈着)や粒子状物質の降下(乾性降下)などにより地上に沈着し森林生態系に蓄積されると共に、森林への蓄積量が飽和量を超えると流下する水の硝酸イオン濃度を上昇させる[1]。
これらは、光化学スモッグや酸性雨などを引き起こす大気汚染原因物質である。主な発生源は、自動車の排気ガスであり、平成4年に制定(平成13年改正)された自動車から排出される窒素酸化物及び粒子状物質の特定地域における総量の削減等に関する特別措置法(自動車NOx・PM法)によって、規制されることになる。
特に毒性の高い二酸化窒素(NO2)は、大気汚染防止法によって環境基準が定められている。 NO2の環境基準:1時間値の1日平均値が0.04ppmから0.06ppmまでのゾーン内またはそれ以下であること。
また、一酸化二窒素(N2O、亜酸化窒素)は二酸化炭素の310倍の温室効果がある。
1970年代にスウェーデンのクルーツェン氏が、成層圏でNOxが触媒作用でオゾン消滅反応に作用していることを指摘し、オゾン層科学に進展がもたらされた[5]。 2008年にN2Oが最大のオゾン層破壊物質であったことが米研究チームにより発表された。[6]
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In atmospheric chemistry, NOx is a generic term for the nitrogen oxides that are most relevant for air pollution, namely nitric oxide (NO) and nitrogen dioxide (NO2).[1][2] These gases contribute to the formation of smog and acid rain, as well as tropospheric ozone.
NOx gases are usually produced from the reaction among nitrogen and oxygen during combustion of fuels, such as hydrocarbons, in air; especially at high temperatures, such as occur in car engines.[1][2][3] In areas of high motor vehicle traffic, such as in large cities, the nitrogen oxides emitted can be a significant source of air pollution. NOx gases are also produced naturally by lightning.
The term NOx is chemistry shorthand for molecules containing one nitrogen and one or more oxygen atom. It is generally meant to include nitrous oxide (N2O),[1] a fairly inert oxide of nitrogen that has many uses as an oxidizer for rockets and car engines, an anesthetic, and a propellant for aerosol sprays and whipped cream. Nitrous oxide plays hardly any role in air pollution, although it may have a significant impact on the ozone layer.[4]
NOy (reactive, free radical) is defined as the sum of NOx plus the NOz compounds produced from the oxidation of NOx which include nitric acid.[5]
Oxygen and nitrogen do not react at ambient temperatures. But at high temperatures, they undergo an endothermic reaction producing various oxides of nitrogen. Such temperatures arise inside an internal combustion engine or a power station boiler, during the combustion of a mixture of air and fuel, and naturally in a lightning flash.
In atmospheric chemistry, the term NOx denotes the total concentration of NO and NO2. During daylight, these concentrations together with that of ozone are in steady state; the ratio of NO to NO2 is determined by the intensity of sunshine (which converts NO2 to NO) and the concentration of ozone (which reacts with NO to again form NO2). The time constant to establish the steady state is 1/k[NO] where k is the rate coefficient of the reaction
for mixing ratio of NO, [NO], = 1 part per billion (ppb), the time constant is 40 minutes; for [NO] = 10 ppb, 4 minutes.[6]:211
When NOx and volatile organic compounds (VOCs) react in the presence of sunlight, they form photochemical smog, a significant form of air pollution, especially in the summer. Children, people with lung diseases such as asthma, and people who work or exercise outside are particularly susceptible to adverse effects of smog such as damage to lung tissue and reduction in lung function.[7]
NO2 is further oxidized in the gas phase during daytime by reaction with OH
where M denotes a third molecule required to stabilize the addition product. Nitric acid (HNO3) is highly soluble in liquid water in aerosol particles or cloud drops.
NO2 also reacts with ozone to form nitrate radical
During the day NO3 is quickly photolyzed back to NO2, but at night it can react with a second NO2 to form dinitrogen pentoxide
N2O5 reacts rapidly with liquid water (in aerosol particles or cloud drops, but not in the gas phase) to form nitric acid HNO3,
These are thought to be the principal pathways for formation of nitric acid in the atmosphere.[6]:224–225 This nitric acid contributes to acid rain or may deposit to soil, where it makes nitrate, which is of use to growing plants. The aqueous phase reaction
is too slow to be of any significance in the atmosphere.[6]:336
Nitric oxide is produced during thunderstorms due to the extreme heat of lightning,[8] and is caused by the splitting of nitrogen molecules. This can result in the production of acid rain, if nitric oxide forms compounds with the water molecules in precipitation.
Scientists Ott et al.[9] estimated that each flash of lightning on average in the several mid-latitude and subtropical thunderstorms studied turned 7 kg (15 lb) of nitrogen into chemically reactive NOx. With 1.4 billion lightning flashes per year, multiplied by 7 kilograms per lightning strike, they estimated the total amount of NOx produced by lightning per year is 8.6 million tonnes. However, NOx emissions resulting from fossil fuel combustion are estimated at 28.5 million tonnes.[10]
A recent discovery indicated that cosmic ray and solar flares can significantly influence the number of lightning strikes occurring on Earth. Therefore, space weather can be a major driving force of lightning-produced atmospheric NOx.[3] It should also be noted that atmospheric constituents such as nitrogen oxides can be stratified vertically in the atmosphere. Ott noted that the lightning-produced NOx is typically found at altitudes greater than 5 km, while combustion and biogenic (soil) NOx are typically found near the sources at near surface elevation (where it can cause the most significant health effects).[11]
Agricultural fertilization and the use of nitrogen fixing plants also contribute to atmospheric NOx, by promoting nitrogen fixation by microorganisms.[12][13]
The three primary sources of NOx in combustion processes:
Thermal NOx formation, which is highly temperature dependent, is recognized as the most relevant source when combusting natural gas. Fuel NOx tends to dominate during the combustion of fuels, such as coal, which have a significant nitrogen content, particularly when burned in combustors designed to minimise thermal NOx. The contribution of prompt NOx is normally considered negligible. A fourth source, called feed NOx is associated with the combustion of nitrogen present in the feed material of cement rotary kilns, at between 300 and 800 °C, where it is also a minor contributor.
Thermal NOx refers to NOx formed through high temperature oxidation of the diatomic nitrogen found in combustion air.[14] The formation rate is primarily a function of temperature and the residence time of nitrogen at that temperature. At high temperatures, usually above 1600 °C (2900 °F), molecular nitrogen (N2) and oxygen (O2) in the combustion air disassociate into their atomic states and participate in a series of reactions.
The three principal reactions (the extended Zel'dovich mechanism) producing thermal NOx are:
All three reactions are reversible. Zeldovich was the first to suggest the importance of the first two reactions.[15] The last reaction of atomic nitrogen with the hydroxyl radical, •HO, was added by Lavoie, Heywood and Keck[16] to the mechanism and makes a significant contribution to the formation of thermal NOx.
It is estimated that transportation fuels cause 54% of the anthropogenic (i.e. human-caused) NOx. The major source of NOx production from nitrogen-bearing fuels such as certain coals and oil, is the conversion of fuel bound nitrogen to NOx during combustion.[14] During combustion, the nitrogen bound in the fuel is released as a free radical and ultimately forms free N2, or NO. Fuel NOx can contribute as much as 50% of total emissions when combusting oil and as much as 80% when combusting coal.
Although the complete mechanism is not fully understood, there are two primary paths of formation. The first involves the oxidation of volatile nitrogen species during the initial stages of combustion. During the release and before the oxidation of the volatiles, nitrogen reacts to form several intermediaries which are then oxidized into NO. If the volatiles evolve into a reducing atmosphere, the nitrogen evolved can readily be made to form nitrogen gas, rather than NOx. The second path involves the combustion of nitrogen contained in the char matrix during the combustion of the char portion of the fuels. This reaction occurs much more slowly than the volatile phase. Only around 20% of the char nitrogen is ultimately emitted as NOx, since much of the NOx that forms during this process is reduced to nitrogen by the char, which is nearly pure carbon.
This third source is attributed to the reaction of atmospheric nitrogen, N2, with radicals such as C, CH, and CH2 fragments derived from fuel, where this cannot be explained by either the aforementioned thermal or fuel processes. Occurring in the earliest stage of combustion, this results in the formation of fixed species of nitrogen such as NH (nitrogen monohydride), HCN (hydrogen cyanide), H2CN (dihydrogen cyanide) and •CN (cyano radical) which can oxidize to NO. In fuels that contain nitrogen, the incidence of prompt NOx is especially minimal and it is generally only of interest for the most exacting emission targets.
NOx reacts with ammonia, moisture, and other compounds to form nitric acid vapor and related particles. Small particles can penetrate deeply into sensitive lung tissue and damage it, causing premature death in extreme cases. Inhalation of such particles may cause or worsen respiratory diseases, such as emphysema or bronchitis, or may also aggravate existing heart disease.[17]
NOx reacts with volatile organic compounds in the presence of sunlight to form and to destroy ozone. Ozone can cause adverse effects such as damage to lung tissue and reduction in lung function mostly in susceptible populations (children, elderly, asthmatics). Ozone can be transported by wind currents and cause health impacts far from the original sources. The American Lung Association estimates that nearly 50 percent of United States inhabitants live in counties that are not in ozone compliance.[18] In South East England, ground level ozone pollution tends to be highest in the countryside and in suburbs, while in central London and on major roads NO emissions are able to "mop up" ozone to form NO2 and oxygen.[19]
NOx also readily reacts with common organic chemicals, and even ozone, to form a wide variety of toxic products: nitroarenes, nitrosamines and also the nitrate radical some of which may cause DNA mutations. Recently another pathway, via NOx, to ozone has been found that predominantly occurs in coastal areas via formation of nitryl chloride when NOx comes into contact with salt mist.[20]
NOx emissions also cause global cooling through the formation of •OH radicals that destroy methane molecules, countering the effect of greenhouse gases. The effect can be significant. For instance, according to the OECD "the large NOx emissions from ship traffic lead to significant increases in hydroxyl (OH), which is the major oxidant in the lower atmosphere. Since reaction with OH is a major way of removing methane from the atmosphere, ship emissions decrease methane concentrations. (Reductions in methane lifetimes due to shipping-based NOx emissions vary between 1.5% and 5% in different calculations)." "In summary, most studies so far indicate that ship emissions actually lead to a net global cooling. However, it should be stressed that the uncertainties with this conclusion are large, in particular for indirect effects, and global temperature is only a first measure of the extent of climate change in any event."[21]
The ultimate destination of much NOx is to end up in the soil as nitrite or nitrate, which are useful to growing plants.
Biodiesel and its blends in general are known to reduce harmful tailpipe emissions such as: carbon monoxide; particulate matter (PM), otherwise known as soot; and unburned hydrocarbon emissions.[22] While earlier studies suggested biodiesel could sometimes decrease NOx and sometimes increase NOx emissions, subsequent investigation has shown that blends of up to 20% biodiesel in USEPA-approved diesel fuel have no significant impact on NOx emissions compared with regular diesel.[23] The state of California uses a special formulation of diesel fuel to produce less NOx relative to diesel fuel used in the other 49 states. This has been deemed necessary by the California Air Resources Board (CARB) to offset the combination of vehicle congestion, warm temperatures, extensive sunlight, PM, and topography that all contribute to the formation of ozone and smog. CARB has established a special regulation for Alternative Diesel Fuels to ensure that any new fuels, including biodiesel, coming into the market do not substantially increase NOx emissions. The reduction of NOx emissions is one of the most important challenges for advances in vehicle technology. While diesel vehicles sold in the US since 2010 are dramatically cleaner than previous diesel vehicles, urban areas continue to seek more ways to reduce the formation of smog and ozone. NOx formation during combustion is associated with a number of factors such as combustion temperature. As such, it can be observed that the vehicle drive cycle, or the load on the engine have more significant impact on NOx emissions than the type of fuel used. This may be especially true for modern, clean diesel vehicles that continuously monitor engine operation electronically and actively control engine parameters and exhaust system operations to limit NOx emission to less than 0.2 g/km. Low-temperature combustion or LTC technology.[2] may help reduce thermal formation of NOx during combustion, however a tradeoff exists as high temperature combustion produces less PM or soot and results in greater power and fuel efficiency.
Selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) reduce post combustion NOx by reacting the exhaust with urea or ammonia to produce nitrogen and water. SCR is now being used in ships,[24] diesel trucks and in some diesel cars. The use of exhaust gas recirculation and catalytic converters in motor vehicle engines have significantly reduced vehicular emissions. NOx was the main focus of the Volkswagen emissions violations.
Other technologies such as flameless oxidation (FLOX) and staged combustion significantly reduce thermal NOx in industrial processes. Bowin low NOx technology is a hybrid of staged-premixed-radiant combustion technology with a major surface combustion preceded by a minor radiant combustion. In the Bowin burner, air and fuel gas are premixed at a ratio greater than or equal to the stoichiometric combustion requirement.[25] Water Injection technology, whereby water is introduced into the combustion chamber, is also becoming an important means of NOx reduction through increased efficiency in the overall combustion process. Alternatively, the water (e.g. 10 to 50%) is emulsified into the fuel oil before the injection and combustion. This emulsification can either be made in-line (unstabilized) just before the injection or as a drop-in fuel with chemical additives for long term emulsion stability (stabilized). Inline emulsified fuel/water mixtures show NOx reductions between 4 and 83%.[26]
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Nitrogen species
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Chemical formulas
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リンク元 | 「窒素酸化物」「nitroxide」「nitrogen oxide」 |
関連記事 | 「N」「NO」 |
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