Issue 12, 2012

Source apportionment of aerosol particles near a steel plant by electron microscopy

Abstract

The size, morphology and chemical composition of 37 715 individual particles collected over 22 sampling days in the vicinity of a large integrated steel production were studied by scanning and transmission electron microscopy. Based on the morphology, chemistry and beam stability the particles were classified into the following fourteen groups: silicates, sea salt, calcium sulfates, calcium carbonates, carbonate–silicate mixtures, sulfate–silicate mixtures, iron oxides, iron mixtures, metal oxide–metals, complex secondary particles, soot, Cl-rich particles, P-rich particles, and other particles. The majority of iron oxide (≈85%) and metal oxide–metal (≈70%) particles as well as ≈20% of the silicate particles are fly ashes from high temperature processes. The emissions from the steel work are dominated by iron oxide particles. For source apportionment, seven source categories and two sectors of local wind direction (industrial and urban background) were distinguished. In both sectors PM10 consists of four major source categories: 35% secondary, 20% industrial, 17% soil and 16% soot in the urban background sector compared to 45% industrial, 20% secondary, 13% soil, and 9% soot in the industrial sector. As the secondary and the soot components are higher in the urban background sector than in the industrial sector, it is concluded that both components predominantly originate from urban background sources (traffic, coal burning, and domestic heating). Abatement measures should not only focus on the steel work but should also include the urban background aerosol.

Graphical abstract: Source apportionment of aerosol particles near a steel plant by electron microscopy

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug 2012
Accepted
01 Nov 2012
First published
14 Nov 2012

J. Environ. Monit., 2012,14, 3257-3266

Source apportionment of aerosol particles near a steel plant by electron microscopy

M. Ebert, D. Müller-Ebert, N. Benker and S. Weinbruch, J. Environ. Monit., 2012, 14, 3257 DOI: 10.1039/C2EM30696D

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