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对多个采石场活动产生的颗粒物(沉积/总悬浮颗粒物)污染的综合评估。

Comprehensive Evaluation of PM (Deposition/TSP) Pollution from Multiple Quarrying Activities.

作者信息

Kara Gülnihal, Çankaya Ali

机构信息

Konya Technical University, Department of Environmental Engineering, Konya 42130, Turkey.

Institution of Graduate Education, Department of Environmental Engineering, Konya Technical University, Konya 42130, Turkey.

出版信息

ACS Omega. 2025 May 13;10(20):20353-20367. doi: 10.1021/acsomega.4c11520. eCollection 2025 May 27.

Abstract

This study, for the first time, analyzed organic matter (OM)-ash fractions, inorganic/organic species, chemical structures, and inhibition effects (EI) in the same sample using a novel procedure. This allowed for an evaluation of the actual contributions of these species to particulate matter (PM) and environmental impacts. Results showed that the mobilities of Al, Co, and potentially toxic elements (PTEs) (As, Cd, Cr, Cu, Pb, and Ni) varied between organic and inorganic phases depending on pH and organic groups. The transition of these elements into the organic phase, along with Ca, contributed to silica polymerization, increased EI in the organic eluate, and enhanced bioavailability in the presence of low water-soluble OM (WOM). Therefore, although Ca abundance reduced EI in the organic eluate, the organic eluate of multiple quarrying areas (MQA), with the lowest OM, exhibited an EI equivalent to the background area (BA). Although ΣPTEs in total suspended particulates (TSP) inorganic eluates decreased compared to total deposition (TD), EI increased. Due to TD-facilitated accumulation-transition and metabolite formation, leading to higher EI in organic eluates. This finding aligned with similar effects observed in aged atmospheric aerosols from the same region. MQA activities significantly contributed to inert dust pollution, Ca, Cu, Cr, K, and Na accumulation, silica and alkali oxide abundance, SOA precursor (e.g., phthalic acid) transformation into more hazardous phthalate esters (PAEs), and new metabolite formation affecting climate change. These activities increased yearly TD and estimated mean TSP by 42 and 41 times, respectively, to 52.9 g/m-year and 1.3 mg/m compared to BA. Despite MQA having the highest TSP-TD, semirural (SRRA) PM influenced by MQA exhibited the highest chemical composition and acute EI. Furthermore, it was found that, aside from Na and Se, there were no significantly enriched elements in MQA when compared to BA.

摘要

本研究首次采用一种新方法,对同一样品中的有机物质(OM)-灰分馏分、无机/有机物种、化学结构和抑制效应(EI)进行了分析。这使得能够评估这些物种对颗粒物(PM)的实际贡献以及环境影响。结果表明,铝、钴和潜在有毒元素(PTEs)(砷、镉、铬、铜、铅和镍)在有机相和无机相之间的迁移率取决于pH值和有机基团。这些元素向有机相的转变,连同钙一起,促进了二氧化硅聚合,增加了有机洗脱液中的EI,并在低水溶性OM(WOM)存在的情况下提高了生物利用度。因此,尽管钙的丰度降低了有机洗脱液中的EI,但多个采石场区域(MQA)的有机洗脱液,其OM含量最低,其EI与背景区域(BA)相当。尽管总悬浮颗粒物(TSP)无机洗脱液中的ΣPTEs与总沉积(TD)相比有所下降,但EI却增加了。由于TD促进了积累-转变和代谢物形成,导致有机洗脱液中的EI更高。这一发现与在同一地区老化大气气溶胶中观察到的类似效应一致。MQA活动对惰性粉尘污染、钙、铜、铬、钾和钠的积累、二氧化硅和碱金属氧化物的丰度、SOA前体(如邻苯二甲酸)向更有害的邻苯二甲酸酯(PAEs)的转化以及影响气候变化的新代谢物形成有显著贡献。与BA相比,这些活动使年TD和估计平均TSP分别增加了42倍和41倍,达到52.9 g/m·年和1.3 mg/m。尽管MQA的TSP-TD最高,但受MQA影响的半农村(SRRA)PM表现出最高的化学成分和急性EI。此外,研究发现,与BA相比,除了钠和硒之外,MQA中没有显著富集的元素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c492/12120662/29fd5c705e6f/ao4c11520_0001.jpg

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