Soot

Short description: Impure carbon particles resulting from the incomplete combustion of hydrocarbons

Emission of soot in the fumes of a large diesel truck, without particle filters

Soot /sʊt/ is a mass of impure carbon particles resulting from the incomplete combustion of hydrocarbons.[1] It is more properly restricted to the product of the gas-phase combustion process but is commonly extended to include the residual pyrolysed fuel particles such as coal, cenospheres, charred wood, and petroleum coke that may become airborne during pyrolysis and that are more properly identified as cokes or char.

Soot causes various types of cancer and lung disease.[2]

## Contents

* 1 Sources
* 2 Description
* 3 Soot formation mechanism
* 4 Hazards
* 5 Soot modeling
* 6 See also
* 7 References
* 8 External links

## Sources

Soot as an airborne contaminant in the environment has many different sources, all of which are results of some form of pyrolysis. They include soot from coal burning, internal-combustion engines,[1] power-plant boilers, hog-fuel boilers, ship boilers, central steam-heat boilers, waste incineration, local field burning, house fires, forest fires, fireplaces, and furnaces. These exterior sources also contribute to the indoor environment sources such as smoking of plant matter, cooking, oil lamps, candles, quartz/halogen bulbs with settled dust, fireplaces, exhaust emissions from vehicles,[3] and defective furnaces. Soot in very low concentrations is capable of darkening surfaces or making particle agglomerates, such as those from ventilation systems, appear black. Soot is the primary cause of "ghosting", the discoloration of walls and ceilings or walls and flooring where they meet. It is generally responsible for the discoloration of the walls above baseboard electric heating units.

The formation of soot depends strongly on the fuel composition.[4][5][6] The rank ordering of sooting tendency of fuel components is: naphthalenes → benzenes → aliphatics. However, the order of sooting tendencies of the aliphatics (alkanes, alkenes, and alkynes) varies dramatically depending on the flame type. The difference between the sooting tendencies of aliphatics and aromatics is thought to result mainly from the different routes of formation. Aliphatics appear to first form acetylene and polyacetylenes, which is a slow process; aromatics can form soot both by this route and also by a more direct pathway involving ring condensation or polymerization reactions building on the existing aromatic structure.[7][8]

## Description

The Intergovernmental Panel on Climate Change (IPCC) adopted the description of soot particles given in the glossary of Charlson and Heintzenberg (1995), “Particles formed during the quenching of gases at the outer edge of flames of organic vapours, consisting predominantly of carbon, with lesser amounts of oxygen and hydrogen present as carboxyl and phenolic groups and exhibiting an imperfect graphitic structure”[9]

Formation of soot is a complex process, an evolution of matter in which a number of molecules undergo many chemical and physical reactions within a few milliseconds.[1] Soot is a powder-like form of amorphous carbon.[citation needed] Gas-phase soot contains polycyclic aromatic hydrocarbons (PAHs).[1][10] The PAHs in soot are known mutagens[11] and are classified as a "known human carcinogen" by the International Agency for Research on Cancer (IARC).[12] Soot forms during incomplete combustion from precursor molecules such as acetylene. It consists of agglomerated nanoparticles with diameters between 6 and 30 nm. The soot particles can be mixed with metal oxides and with minerals and can be coated with sulfuric acid.[1][13]

## Soot formation mechanism

Many details of soot formation chemistry remain unanswered and controversial, but there have been a few agreements:[1]

* Soot begins with some precursors or building blocks.
* Nucleation of heavy molecules occurs to form particles.
* Surface growth of a particle proceeds by adsorption of gas phase molecules.
* Coagulation happens via reactive particle–particle collisions.
* Oxidation of the molecules and soot particles reduces soot formation.

## Hazards

The black staining on the power car of this Midland Mainline InterCity 125 High Speed Train is the result of soot building up on the train's surface.

Soot, particularly diesel exhaust pollution, accounts for over one quarter of the total hazardous pollution in the air.[3][14]

Among these diesel emission components, particulate matter has been a serious concern for human health due to its direct and broad impact on the respiratory organs. In earlier times, health professionals associated PM10 (diameter < 10 μm) with chronic lung disease, lung cancer, influenza, asthma, and increased mortality rate. However, recent scientific studies suggest that these correlations be more closely linked with fine particles (PM2.5) and ultra-fine particles (PM0.1).[1]

Long-term exposure to urban air pollution containing soot increases the risk of coronary artery disease.[15]

Diesel exhaust (DE) gas is a major contributor to combustion-derived particulate-matter air pollution.[3] In human experimental studies using an exposure chamber setup, DE has been linked to acute vascular dysfunction and increased thrombus formation.[16][17] This serves as a plausible mechanistic link between the previously described association between particulate matter air pollution and increased cardiovascular morbidity and mortality.[citation needed]

Soot also tends to form in chimneys in domestic houses possessing one or more fireplaces. If a large deposit collects in one, it can ignite and create a chimney fire. Regular cleaning by a chimney sweep should eliminate the problem.[18]

## Soot modeling

Soot mechanism is difficult to model mathematically because of the large number of primary components of diesel fuel, complex combustion mechanisms, and the heterogeneous interactions during soot formation.[1] Soot models are broadly categorized into three subgroups: empirical (equations that are adjusted to match experimental soot profiles), semi-empirical (combined mathematical equations and some empirical models which used for particle number density and soot volume and mass fraction), and detailed theoretical mechanisms (covers detailed chemical kinetics and physical models in all phases) are usually available in the literature for soot models.[1]

Empirical models use correlations of experimental data to predict trends in soot production. Empirical models are easy to implement and provide excellent correlations for a given set of operating conditions. However, empirical models cannot be used to investigate the underlying mechanisms of soot production. So, these models are not flexible enough to handle changes in operating conditions. They are only useful for testing previously established designed experiments under specific conditions.[1]

Second, semi-empirical models solve rate equations that are calibrated using experimental data. Semi-empirical models reduce computational costs primarily by simplifying the chemistry in soot formation and oxidation. Semi-empirical models reduce the size of chemical mechanisms and use simpler molecules, such as acetylene as precursors.[1] Detailed theoretical models use extensive chemical mechanisms containing hundreds of chemical reactions in order to predict concentrations of soot. Detailed theoretical soot models contain all the components present in the soot formation with a high level of detailed chemical and physical processes.[1]

Such comprehensive models (detailed models) usually take high financial burden for programming and operating, and much computational time to produce a converged solution. On the other hand, empirical and semi-empirical models ignore some of the details in order to make complex model simple and to reduce the computational cost and time. Thanks to recent technological progress in computation, it becomes more feasible to use detailed theoretical models and obtain more realistic results. However, further advancement of comprehensive theoretical models must be preceded by the more detailed and accurate formation mechanisms.[1]

On the other hand, models that are based on a phenomenological description have found wide use recently. Phenomenological soot models, which may be categorized as semi-empirical models, correlate empirically observed phenomena in a way that is consistent with the fundamental theory, but is not directly derived from the theory. Phenomenological models use sub-models developed to describe the different processes (or phenomena) observed during the combustion process. These sub-models can be empirically developed from observation or by using basic physical and chemical relations. Advantages of phenomenological models are that they are quite reliable and yet not so complicated. So, they are useful, especially when the accuracy of the model parameters is low. For example, the phenomenological models can predict the soot formation even when several operating conditions are changed in a system and the accuracy cannot be guaranteed. Examples of sub-models of phonological empirical models could be listed as spray model, lift-off model, heat release model, ignition delay model, etc.[1]

## See also

* Activated carbon
* Atmospheric particulate matter
* Bistre
* Black carbon
* Carbon black
* Colorant
* Creosote
* Diesel particulate matter
* Fullerene
* Indian ink
* Rolling coal
* Soot blower

## References

1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Omidvarborna (2015). "Recent studies on soot modeling for diesel combustion". Renewable and Sustainable Energy Reviews 48: 635–647. doi:10.1016/j.rser.2015.04.019.
2. ↑
* Bond, T. C.; Doherty, S. J.; Fahey, D. W.; Forster, P. M.; Berntsen, T.; Deangelo, B. J.; Flanner, M. G.; Ghan, S. et al. (2013). "Bounding the role of black carbon in the climate system: A scientific assessment". Journal of Geophysical Research: Atmospheres 118 (11): 5380. doi:10.1002/jgrd.50171. Bibcode: 2013JGRD..118.5380B. https://deepblue.lib.umich.edu/bitstream/2027.42/99106/1/jgrd50171.pdf.
* Juliet Eilperin (2013-11-26). "Black carbon ranks as second-biggest human cause of global warming". The Washington Post. https://www.washingtonpost.com/national/health-science/black-carbon-ranks-as-second-biggest-human-cause-of-global-warming/2013/01/15/6d4e542a-5f2d-11e2-9940-6fc488f3fecd_story.html?tid=pm_pop.
3. ↑ 3.0 3.1 3.2 Omidvarborna (2014). "Characterization of particulate matter emitted from transit buses fueled with B20 in idle modes". Journal of Environmental Chemical Engineering 2 (4): 2335–2342. doi:10.1016/j.jece.2014.09.020.
4. ↑ Seinfeld, John H.; Pandis, Spyros N. (2006). Atmospheric Chemistry and Physics : From Air Pollution to Climate Change (2nd ed.). John Wiley & Sons. ISBN 0-471-72018-6.
5. ↑ "Multiscale characterization of exhaust and crankcase soot extracted from heavy-duty diesel engine and implications for DPF ash". Fuel 282: 118878. August 2020. doi:10.1016/j.fuel.2020.118878.
6. ↑ "Effects of Diesel Soot Composition and Accumulated Vehicle Mileage on Soot Oxidation Characteristics". ACS Energy & Fuels 30: 8479–8490. September 2016. doi:10.1021/acs.energyfuels.6b01304.
7. ↑ Graham, S. C.; Homer, J. B.; Rosenfeld, J. L. J. (1975). "The formation and coagulation of soot aerosols generated in pyrolysis of aromatic hydrocarbons". Proc. Roy. Soc. Lond. A 344: 259–285. doi:10.1098/rspa.1975.0101.
8. ↑ Flagan, R. C.; Seinfeld, J. H. (1988). Fundamentals of Air Pollution Engineering. Englewood Cliffs, NJ: Prentice-Hall. ISBN 0-13-332537-7.
9. ↑ Charlson, R. J.; Heintzenberg, J., eds (1995). Aerosol Forcing of Climate. New York, NY: John Wiley & Sons. p. 406. ISBN 0-471-95693-7.
10. ↑ Rundel, Ruthann, "Polycyclic Aromatic Hydrocarbons, Phthalates, and Phenols", in Indoor Air Quality Handbook, John Spengleer, Jonathan M. Samet, John F. McCarthy (eds), pp. 34.1-34.2, 2001
11. ↑ Rundel, Ruthann, "Polycyclic Aromatic Hydrocarbons, Phthalates, and Phenols", in Indoor Air Quality Handbook, John Spengleer, Jonathan M. Samet, John F. McCarthy (eds), pp. 34.18-34.21, 2001
12. ↑ "Soots (IARC Summary & Evaluation, Volume 35, 1985)". Inchem.org. 1998-04-20. http://www.inchem.org/documents/iarc/vol35/soots.html.
13. ↑ Niessner, R. (2014). "The Many Faces of Soot: Characterization of Soot Nanoparticles Produced by Engines". Angew. Chem. Int. Ed. 53 (46): 12366–12379. doi:10.1002/anie.201402812. PMID 25196472.
14. ↑ "Health Concerns Associated with Excessive Idling". Nctcog.org. http://www.nctcog.org/trans/air/vehicles/health.asp.
15. ↑ "Long-Term Exposure to Air Pollution and Incidence of Cardiovascular Events in Women" Kristin A. Miller, David S. Siscovick, Lianne Sheppard, Kristen Shepherd, Jeffrey H. Sullivan, Garnet L. Anderson, and Joel D. Kaufman, in New England Journal of Medicine February 1, 2007
16. ↑ Lucking, Andrew J. et al. (2008). "Diesel exhaust inhalation increases thrombus formation in man". European Heart Journal 29 (24): 3043–3051. doi:10.1093/eurheartj/ehn464. PMID 18952612.
17. ↑ Törnqvist, Håkan et al. (2007). "Persistent Endothelial Dysfunction in Humans after Diesel Exhaust Inhalation". American Journal of Respiratory and Critical Care Medicine 176 (4): 395–400. doi:10.1164/rccm.200606-872OC. PMID 17446340.
18. ↑ "Gr8fires". 2015-02-22. https://blog.gr8fires.co.uk/2015/02/22/how-to-remove-soot-from-a-chimney/.

## External links

* "Blacks". Encyclopedia Americana. 1920.

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