烹饪活动后室内空气化学的测量和建模研究

IF 4.3 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL Environmental Science: Processes & Impacts Pub Date : 2023-08-14 DOI:10.1039/D3EM00167A
Helen L. Davies, Catherine O'Leary, Terry Dillon, David R. Shaw, Marvin Shaw, Archit Mehra, Gavin Phillips and Nicola Carslaw
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引用次数: 0

摘要

家庭烹饪是室内空气污染物的一个来源,包括会影响室内空气质量的挥发性有机化合物(voc)。然而,烹饪过程中挥发性有机化合物的实时排放并没有得到很好的表征,同样,人们对由此产生的二次化学反应也知之甚少。本研究采用选择性离子流管质谱法(SIFT-MS),在室内半真实环境下,实时监测一份鸡肉蔬菜炒饭烹饪过程中挥发性有机化合物的排放。挥发性有机化合物的排放主要是醇类(占总排放量的70%),但也含有一系列醛类(14%)和萜烯类(5%),主要原因分别是油的加热和香料的制备和加热。然后使用Python中的室内化学模型(INCHEM-Py)模拟与烹饪相关的直接VOC排放,以研究由此产生的二次化学。建模显示,挥发性有机化合物的浓度主要是直接排放的,次生产物的贡献很小,尽管次生产物比直接排放的物质寿命更长。烹饪后,羟基自由基浓度降低了86%,而有机过氧自由基浓度增加了700%以上,随后形成二次有机硝酸盐、过氧酰基硝酸盐(pan)和甲醛。单萜烯的排放被证明可以驱动二次甲醛的形成,尽管产生的浓度相对较小(平均为60毫帕)。模拟条件的敏感性分析表明,室外臭氧和NOx浓度增加(分别为2.9倍和9倍),室内二次产物生成增幅最大(有机硝酸盐、pan和甲醛产量分别增加约400%、200%和600%)。考虑到气候变化很可能导致未来臭氧浓度的增加,并且由于气温上升而增加的开窗也很可能,未来家庭中室内氧化剂的浓度可能会更高。因此,这项研究表明,烹饪可能是未来室内二次污染物的一个更重要的来源。
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A measurement and modelling investigation of the indoor air chemistry following cooking activities†

Domestic cooking is a source of indoor air pollutants, including volatile organic compounds (VOCs), which can impact on indoor air quality. However, the real-time VOC emissions from cooking are not well characterised, and similarly, the resulting secondary chemistry is poorly understood. Here, selected-ion flow-tube mass spectrometry (SIFT-MS) was used to monitor the real-time VOC emissions during the cooking of a scripted chicken and vegetable stir-fry meal, in a room scale, semi-realistic environment. The VOC emissions were dominated by alcohols (70% of total emission), but also contained a range of aldehydes (14%) and terpenes (5%), largely attributable to the heating of oil and the preparation and heating of spices, respectively. The direct cooking-related VOC emissions were then simulated using the Indoor Chemical Model in Python (INCHEM-Py), to investigate the resulting secondary chemistry. Modelling revealed that VOC concentrations were dominated by direct emissions, with only a small contribution from secondary products, though the secondary species were longer lived than the directly emitted species. Following cooking, hydroxyl radical concentrations reduced by 86%, while organic peroxy radical levels increased by over 700%, later forming secondary organic nitrates, peroxyacylnitrates (PANs) and formaldehyde. Monoterpene emissions were shown to drive the formation of secondary formaldehyde, albeit to produce relatively modest concentrations (average of 60 ppt). Sensitivity analysis of the simulation conditions revealed that increasing the outdoor concentrations of ozone and NOx species (2.9× and 9×, respectively) resulted in the greatest increase in secondary product formation indoors (≈400%, 200% and 600% increase in organic nitrates, PANs and formaldehyde production, respectively). Given the fact that climate change is likely to result in increased ozone concentrations in the future, and that increased window-opening in response to rising temperatures is also likely, higher concentrations of indoor oxidants are likely in homes in the future. This work, therefore, suggests that cooking could be a more important source of secondary pollutants indoors in the future.

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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
期刊最新文献
Correction: Exploring the variability of PFAS in urban sewage: a comparison of emissions in commercial versus municipal urban areas. Validation of a laboratory spray generation system and its use in a comparative study of hexamethylene diisocyanate (HDI) evaluation methods. Fluorinated aromatic PBCTF and 6:2 diPAP in bridge and traffic paints. Sorption of metal ions onto PET-derived microplastic fibres. Reduction of hexavalent chromium by compost-derived dissolved organic matter.
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