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未使用和使用过的加热不燃烧烟草制品和传统香烟中的总多环芳烃和生物可利用多环芳烃。

Total and bioavailable polycyclic aromatic hydrocarbons in unused and operated heat-not-burn tobacco products and conventional cigarettes.

机构信息

Laboratory of Aquatic Chemistry, School of Chemical and Environmental Engineering, Technical University of Crete, GR-73100, Chania, Crete, Greece.

Markes International Ltd, 1000B Central Park, Western Avenue, CF31 3RT, Bridgend, United Kingdom.

出版信息

Chemosphere. 2023 Sep;335:139050. doi: 10.1016/j.chemosphere.2023.139050. Epub 2023 May 27.

Abstract

Tobacco product waste poses a global environmental issue, affecting urban and coastal areas alike. The present studies report, for the first time, the total and bioavailable polycyclic aromatic hydrocarbons (PAHs) concentrations in unused and operated heat-not-burn (HnBs) tobacco products. To enable direct comparisons, identical sets of studies were conducted using conventional cigarettes (CCs). Five low-molecular PAHs were determined in HnBs at total concentrations that were of the same order before and after operation (ΣPAH = 47.37 ± 3.44 ng unit and ΣPAH = 69.36 ± 5.78 ng unit in unused and used HnBs, respectively). The incomplete combustion of organics during smoking of CCs, yielded substantially higher amounts of PAHs with their sum (ΣPAHs = 1449 ± 113 ng unit) being >20 times larger than those in HnBs. The tobacco and filter were the most contaminated parts in HnBs. In unused CCs, tobacco had the highest PAHs load and after smoking, the spent filter was the most contaminated part, containing ∼80% of the total amount of PAHs. Naphthalene was the most abundant PAH detected in all tobacco products. Despite the high total PAH concentrations found in smoked CCs, the sums of the bioavailable PAH concentrations were of the same order in all tested tobacco products (ΣPAH = 61.38 ± 1.79 ng unit in unused HnBs, ΣPAH = 70.87 ± 7.67 ng unit in used HnBs, ΣPAH = 66.92 ± 5.95 ng unit in unused CCs, and ΣPAH = 47.94 ± 1.26 ng unit in smoked CCs). This finding was related to smoking affecting PAHs' leachability from CCs and delaying their desorption from the solid matrix. Adjusting the pH, salt and humic acids content at environmentally relevant values did not affect PAHs leaching at 24 h of soaking. Finally, the leaching behavior of PAHs in natural waters (river water, rainwater, and seawater) was found similar to that in ultrapure water, experimentally verifying the ability of tobacco product waste to leach PAHs into the aquatic environment.

摘要

烟草制品废物是一个全球性的环境问题,对城市和沿海地区都有影响。本研究首次报道了未使用和使用过的加热不燃烧(HnB)烟草制品中总多环芳烃(PAHs)和可生物利用 PAHs 的浓度。为了进行直接比较,使用传统卷烟(CC)进行了相同的研究。在未使用和使用过的 HnB 中,总浓度分别为 47.37 ± 3.44ng 单位和 69.36 ± 5.78ng 单位,确定了 5 种低分子量 PAHs。在 CC 吸烟过程中,有机物的不完全燃烧产生了大量的 PAHs,其总和(ΣPAHs=1449±113ng 单位)比 HnB 中的 PAHs 高 20 多倍。烟草和过滤嘴是 HnB 中污染最严重的部分。在未使用的 CC 中,烟草中 PAHs 含量最高,吸烟后,用过的过滤嘴是污染最严重的部分,含有约 80%的总 PAHs。萘是所有烟草制品中含量最丰富的 PAH。尽管在使用过的 CC 中发现了高浓度的总 PAHs,但所有测试的烟草制品中可生物利用的 PAH 浓度总和处于同一水平(未使用的 HnB 中 ΣPAH=61.38±1.79ng 单位,使用过的 HnB 中 ΣPAH=70.87±7.67ng 单位,未使用的 CC 中 ΣPAH=66.92±5.95ng 单位,使用过的 CC 中 ΣPAH=47.94±1.26ng 单位)。这一发现与吸烟影响 CCs 中 PAHs 的浸出率以及延迟其从固体基质中解吸有关。将 pH 值、盐度和腐殖酸含量调整到环境相关值,不会影响 24 小时浸泡时的 PAHs 浸出率。最后,发现天然水中(河水、雨水和海水)的 PAHs 浸出行为与超纯水相似,从实验上验证了烟草制品废物将 PAHs 浸出到水环境中的能力。

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