Department of Earth Science and Engineering, Imperial College London, South Kensington Campus, Prince Consort Road, SW7 2AZ, London, United Kingdom.
Department of Earth Science and Engineering, Imperial College London, South Kensington Campus, Prince Consort Road, SW7 2AZ, London, United Kingdom.
Environ Pollut. 2023 Jul 15;329:121664. doi: 10.1016/j.envpol.2023.121664. Epub 2023 Apr 19.
Improving urban air quality is a global challenge. To implement successful abatement measures that reduce atmospheric particulate matter (APM) and associated metal concentrations, precise source apportionment is needed. For this, apportioning contributions from coal and biomass burning and differentiating these from non-exhaust traffic emissions in urban APM is critical. Recent studies characterising the metal isotope composition of urban APM, and potential source materials suggested that non-traditional isotope systems could prove unique fingerprinting tools. Zinc isotopes should be able to separate APM derived from uncontrolled combustion (fly ash, isotopically heavy) from non-exhaust traffic sources (tyre and brake wear, intermediate) and from controlled industrial emissions (flue gas, light). To test this hypothesis, we determined zinc isotope ratios of APM (TSP, PM, PM) in Beijing (coal combustion for residential heating) and Varanasi (biomass burning in pre-monsoon periods). In Beijing, δZn values of PM ranged from -0.41 to +1.01‰ in 2015 (avg = +0.25 ± 0.50‰, n = 19). Aerosols (including TSP, PM and PM samples) from the heating period were significantly (t-test, p < 0.001) heavier (avg = +0.90 ± 0.12‰, n = 7) than those from the non-heating period (avg = +0.14 ± 0.36‰, n = 23). Average δZn values of PM in Varanasi in spring 2015 were +0.82 ± 0.11‰ (n = 4). Extent and direction of isotope fractionation is in line with that expected from theoretical models and the isotope signatures observed agree with previously determined ratios of source materials. Our study links for the first time comprehensively the heavy zinc isotope compositions in APM to coal and biomass burning and shows that zinc isotope compositions of aerosols can discriminate between non-exhaust traffic and combustion sources.
改善城市空气质量是全球性挑战。为了实施成功的减排措施,降低大气颗粒物(APM)和相关金属浓度,需要精确的源分配。为此,将煤和生物质燃烧的贡献与城市 APM 中的非排放交通排放区分开来至关重要。最近研究了城市 APM 中金属同位素组成和潜在源材料的特征,表明非传统同位素系统可能成为独特的指纹识别工具。锌同位素应该能够将源自无控制燃烧(粉煤灰,同位素较重)的 APM 与非排放交通源(轮胎和刹车片磨损,中间)和来自受控工业排放(烟气,轻)区分开来。为了验证这一假设,我们测定了北京(居民供暖用煤燃烧)和瓦拉纳西(季风前生物质燃烧)的 APM(TSP、PM、PM)中的锌同位素比值。2015 年,北京 PM 的 δZn 值范围为-0.41 至+1.01‰(平均值为+0.25±0.50‰,n=19)。供暖期的气溶胶(包括 TSP、PM 和 PM 样品)比非供暖期(平均值为+0.14±0.36‰,n=23)明显更重(t 检验,p<0.001)(平均值为+0.90±0.12‰,n=7)。2015 年春季瓦拉纳西 PM 的平均 δZn 值为+0.82±0.11‰(n=4)。同位素分馏的程度和方向与理论模型所预期的一致,观察到的同位素特征与先前确定的源材料比值一致。我们的研究首次将 APM 中的重锌同位素组成与煤和生物质燃烧联系起来,并表明气溶胶的锌同位素组成可以区分非排放交通和燃烧源。