Department of Earth Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, 741246, Nadia, India.
School of Engineering, Indian Institute of Technology (IIT) Mandi, Kamand, Himachal Pradesh, 175075, India.
Environ Sci Pollut Res Int. 2022 Jun;29(26):40252-40261. doi: 10.1007/s11356-022-20183-4. Epub 2022 Apr 11.
We hypothesize that firework events involving the combustion of charcoal fuel, organic binders, metal salts, and cellulose-based wrapping material could be significant transient sources of aerosol brown carbon (BrC). To test this, we couple high time-resolution (1 min) measurements of black carbon (BC) and BrC absorption from a 7-wavelength aethalometer with time-integrated (12-24 h) measurements of filter extracts, i.e., UV-visible, fluorescence, and Fourier-transformed infrared (FT-IR) signatures of BrC, total and water-soluble organic carbon (OC and WSOC), ionic species, and firework tracer metals during a sampling campaign covering the Diwali fireworks episode in India. In sharp contrast to BC, BrC absorption shows a distinct and considerable rise of 2-4 times during the Diwali period, especially during the hours of peak firework activity, as compared to the background. Fluorescence profiles suggest enrichment of humic-like substances (HULIS) in the firework plume, while the enhancement of BrC absorption in the 400-500 nm range suggests the presence of nitroaromatic compounds (NACs). Considerable contributions of WSOC and secondary organics to OC (44.1% and 31.2%, respectively) and of the water-soluble fraction of BrC to total BrC absorption (71.0%) during the Diwali period point toward an atmospherically processed, polar signature of firework-related BrC, which is further confirmed by FT-IR profiles. This aqueous BrC exerts a short-lived but strong effect on atmospheric forcing (12.0% vis-à-vis BC in the UV spectrum), which could affect tropospheric chemistry via UV attenuation and lead to a stabilization of the post-Diwali atmosphere, resulting in enhanced pollutant build-up and exposure.
我们假设,涉及木炭燃料、有机粘合剂、金属盐和纤维素包装材料燃烧的烟花事件可能是气溶胶棕色碳 (BrC) 的重要瞬态来源。为了验证这一点,我们将高时间分辨率(1 分钟)的黑碳 (BC) 和 BrC 吸收测量与时间积分(12-24 小时)的滤膜提取物测量相结合,即 UV-可见、荧光和傅里叶变换红外 (FT-IR) 的 BrC、总有机碳 (OC) 和水溶性有机碳 (WSOC)、离子物种和烟花示踪金属的特征,在一次采样活动中,涵盖了印度排灯节烟花事件。与 BC 形成鲜明对比的是,BrC 吸收在排灯节期间明显上升了 2-4 倍,尤其是在烟花活动高峰时段,与背景相比,上升了 2-4 倍。荧光剖面表明富里酸类物质 (HULIS) 在烟花羽流中富集,而在 400-500nm 范围内 BrC 吸收的增强表明存在硝基芳香族化合物 (NACs)。在排灯节期间,OC 中 WSOC 和二次有机物的大量贡献(分别为 44.1%和 31.2%)以及总 BrC 吸收中水溶性 BrC 部分的大量贡献(71.0%)表明,烟花相关 BrC 具有大气处理的极性特征,这进一步通过 FT-IR 剖面得到证实。这种水溶性 BrC 对大气强迫产生了短暂但强烈的影响(在 UV 光谱中相对于 BC 为 12.0%),这可能通过紫外线衰减影响对流层化学,并导致排灯节后大气稳定,从而导致污染物积聚和暴露增加。