Peking University, College of Environmental Science and Engineering, Beijing, 100871, China.
Photochem Photobiol Sci. 2011 Feb;10(2):280-91. doi: 10.1039/c0pp90039g. Epub 2011 Jan 20.
Air pollution will be directly influenced by future changes in emissions of pollutants, climate, and stratospheric ozone, and will have significant consequences for human health and the environment. UV radiation is one of the controlling factors for the formation of photochemical smog, which includes tropospheric ozone (O(3)) and aerosols; it also initiates the production of hydroxyl radicals (˙OH), which control the amount of many climate- and ozone-relevant gases (e.g., methane and HCFCs) in the atmosphere. Numerical models predict that future changes in UV radiation and climate will modify the trends and geographic distribution of ˙OH, thus affecting the formation of photochemical smog in many urban and regional areas. Concentrations of ˙OH are predicted to decrease globally by an average of 20% by 2100, with local concentrations varying by as much as a factor of two above and below current values. However, significant differences between modelled and measured values in a limited number of case studies show that chemistry of hydroxyl radicals in the atmosphere is not fully understood. Photochemically produced tropospheric ozone is projected to increase. If emissions of anthropogenic air pollutants from combustion of fossil fuels, burning of biomass, and agricultural activities continue to increase, concentrations of tropospheric O(3) will tend to increase over the next 20-40 years in certain regions of low and middle latitudes because of interactions of emissions, chemical processes, and climate change. Climate-driven increases in temperature and humidity will also increase production of tropospheric O(3) in polluted regions, but reduce it in more pristine regions. Higher temperatures tend to increase emissions of nitrogen oxides (NO(x)) from some soils and release of biogenic volatile organic compounds (VOCs) from vegetation, leading to greater background concentrations of ozone in the troposphere. The net effects of future changes in UV radiation, meteorological conditions, and anthropogenic emissions may be large, thus posing challenges for prediction and management of air quality. Aerosols composed of organic substances have a major role in both climate and air quality, and contribute a large uncertainty to the energy budget of the atmosphere. These aerosols are mostly formed via the UV-initiated oxidation of VOCs from anthropogenic and biogenic sources, although the details of the chemistry are still poorly understood and current models under-predict their abundance. A better understanding of their formation, chemical composition, and optical properties is required to assess their significance for air quality and to better quantify their direct and indirect radiative forcing of climate. Emissions of compounds containing fluorine will continue to have effects on the chemistry of the atmosphere and on climate change. The HCFCs and HFCs used as substitutes for ozone-depleting CFCs can break down into trifluoroacetic acid (TFA), which will accumulate in oceans, salt lakes, and playas. Based on historical use and projections of future uses, including new products entering the market, such as the fluoro-olefins, increased loadings of TFA in these environmental sinks will be small. Even when added to existing amounts from natural sources, risks to humans or the environment from the historical use of CFCs or continued use of their replacements is judged to be negligible.
空气污染将直接受到污染物排放、气候和平流层臭氧未来变化的影响,并将对人类健康和环境产生重大影响。紫外线辐射是光化学烟雾形成的控制因素之一,其中包括对流层臭氧(O(3))和气溶胶;它还引发了羟基自由基(˙OH)的产生,控制着大气中许多与气候和臭氧相关的气体(如甲烷和氟氯烃)的含量。数值模型预测,未来紫外线辐射和气候的变化将改变˙OH 的趋势和地理分布,从而影响许多城市和地区光化学烟雾的形成。预计到 2100 年,全球˙OH 浓度将平均下降 20%,而局部浓度在当前值上下波动可达两倍。然而,在为数不多的案例研究中,模型预测值与实测值之间存在显著差异,这表明大气中羟基自由基的化学性质尚未完全了解。光化学生成的对流层臭氧预计会增加。如果化石燃料燃烧、生物质燃烧和农业活动产生的人为空气污染物排放继续增加,那么在低中纬度的某些地区,由于排放、化学过程和气候变化的相互作用,未来 20-40 年中,对流层 O(3)的浓度将趋于增加。气候驱动的温度和湿度升高也会增加污染地区的对流层 O(3)生成,但会减少更原始地区的生成。较高的温度往往会增加某些土壤中氮氧化物(NO(x))的排放,并导致植被中生物源挥发性有机化合物(VOCs)的释放,从而导致对流层中臭氧的背景浓度增加。未来紫外线辐射、气象条件和人为排放变化的净效应可能很大,因此对空气质量的预测和管理构成挑战。由有机物质组成的气溶胶在气候和空气质量方面都起着重要作用,并且对大气的能量平衡产生了很大的不确定性。这些气溶胶主要是通过人为和生物源的 VOCs 的紫外线引发氧化形成的,尽管其化学细节仍不清楚,而且当前的模型对其丰度的预测不足。需要更好地了解它们的形成、化学成分和光学特性,以评估它们对空气质量的重要性,并更好地量化它们对气候的直接和间接辐射强迫。含氟化合物的排放将继续对大气化学和气候变化产生影响。用作消耗臭氧层物质(CFCs)替代品的氢氯氟烃(HCFCs)和氢氟碳化物(HFCs)可分解为三氟乙酸(TFA),TFA 将在海洋、盐湖和干盐湖中积累。基于历史用途和对未来用途的预测,包括进入市场的新产品,如氟烯烃,这些环境汇中的 TFA 负荷增加将很小。即使将其与来自天然来源的现有量相加,从 CFCs 的历史使用或其替代品的持续使用中对人类或环境造成的风险也被认为是微不足道的。