Oxy-fuel combustion process

Oxyfuel CCS power plant operation

Oxy-fuel combustion is the process of burning a fuel using pure oxygen instead of air as the primary oxidant. Since the nitrogen component of air is not heated, fuel consumption is reduced, and higher flame temperatures are possible. Historically, the primary use of oxy-fuel combustion has been in welding and cutting of metals, especially steel, since oxy-fuel allows for higher flame temperatures than can be achieved with an air-fuel flame.[1]

There is currently research being done in firing fossil-fueled power plants with an oxygen-enriched gas mix instead of air. Almost all of the nitrogen is removed from input air, yielding a stream that is approximately 95% oxygen. Firing with pure oxygen would result in too high a flame temperature, so the mixture is diluted by mixing with recycled flue gas, or staged combustion. The recycled flue gas can also be used to carry fuel into the boiler and ensure adequate convective heat transfer to all boiler areas. Oxy-fuel combustion produces approximately 75% less flue gas than air fueled combustion and produces exhaust consisting primarily of CO2 and H2O (see figure).

The justification for using oxy-fuel is to produce a CO2 rich flue gas ready for sequestration. Oxy-fuel combustion has significant advantages over traditional air-fired plants. Among these are:

Economically speaking this method costs more than a traditional air-fired plant. The main problem has been separating oxygen from the air. This process needs lots of energy, nearly 15% of production by a coal-fired power station can be consumed for this process. However, a new technology which is not yet practical called chemical looping combustion[2] can be used to reduce this cost. In chemical looping combustion, the oxygen required to burn the coal is produced internally by oxidation and reduction reactions, as opposed to using more expensive methods of generating oxygen by separating it from air.[3]

At present in the absence of any need to reduce CO2 emissions, oxy-fuel is not competitive. However, oxy-fuel is a viable alternative to removing CO2 from the flue gas from a conventional air-fired fossil fuel plant. However, an oxygen concentrator might be able to help, as it simply removes nitrogen.

In industries other than power generation, oxy-fuel combustion can be competitive due to higher sensible heat availability.

Oxy-fuel combustion is common in various aspects of metal production.

The glass industry has been converting to oxy-fuel since the early 1990s because glass furnaces require a temperature of approximately 2800 degrees F, which is not attainable at adiabatic flame temperatures for air-fuel combustion unless heat is regenerated between the flue stream and the incoming air stream. Historically, glass furnace regenerators were large and expensive high temperature brick ducts filled with brick arranged in a checkerboard pattern to capture heat as flue gas exits the furnace. When the flue duct is thoroughly heated, air flow is reversed and the flue duct becomes the air inlet, releasing its heat into the incoming air, and allowing for higher furnace temperatures than can be attained with air-fuel only. Two sets of regenerative flue ducts allowed for the air flow to be reversed at regular intervals, and thus maintain a high temperature in the incoming air. By allowing new furnaces to be built without the expense of regenerators, and especially with the added benefit of nitrogen oxide reduction, which allows glass plants to meet emission restrictions, oxy-fuel is cost effective without the need to reduce CO2 emissions. Oxy-fuel combustion also reduces CO2 release at the glass plant location, although this may be offset by CO2 production due to electric power generation which is necessary to produce oxygen for the combustion process.

Oxy-fuel combustion may also be cost effective in the incineration of low BTU value hazardous waste fuels.

Oxy-fuel combustion is often combined with staged combustion for nitrogen oxide reduction, since pure oxygen can stabilize combustion characteristics of a flame.

Pilot Plants

There are pilot plants undergoing initial proof-of-concept testing to evaluate the technologies for scaling up to commercial plants, including

White Rose Plant

One case study of oxy-fuel combustion is the attempted White Rose plant in North Yorkshire, United Kingdom. The planned project was an oxy-fuel power plant coupled with air separation to capture two million tons of carbon dioxide per year. The carbon dioxide would then be delivered by pipeline to be sequestered in a saline aquifer beneath the North Sea.[7] However, in late 2015 and early 2016, following withdrawal of funding by the Drax Group and the U.K. government, construction was halted.[8] The unforeseen loss of the federal CCS Commercialisation Programme, along with decreased subsidies for renewable energy, left the White Rose Plant with insufficient funds to continue development.[7]

See also

References

  1. Markewitz, Peter; Leitner, Walter; Linssen, Jochen; Zapp, Petra; Müller, Thomas; Schreiber, Andrea (2012-03-01). "Worldwide innovations in the development of carbon capture technologies and the utilization of CO2". Energy & Environmental Science. 6: 7281–7385. doi:10.1039/C2EE03403D. Retrieved 2016-10-04.
  2. "Oxy Fuel CO2 Carbon Capture and Sequestration Technology Method - Power Plant CCS". www.powerplantccs.com.
  3. "chemical-looping-combustion | netl.doe.gov". www.netl.doe.gov. Retrieved 2017-05-05.
  4. Spero, Chris; Yamada, Toshihiko; Nelson, Peter; Morrison, Tony; Bourhy-Weber, Claire. "Callide Oxyfuel Project – Combustion and Environmental Performance" (PDF). www.eventspro.net. 3rd Oxyfuel Combustion Conference. Retrieved May 5, 2017.
  5. "Ciudad de la Energía". www.ciuden.es. Fundación Ciudad de la Energía. Retrieved May 5, 2017.
  6. "NetPower". netpower.com. Retrieved May 5, 2017.
  7. 1 2 "White Rose CCS Project | Global Carbon Capture and Storage Institute". www.globalccsinstitute.com. Retrieved 2017-05-05.
  8. "Carbon Capture and Sequestration Technologies @ MIT". sequestration.mit.edu. Retrieved 2017-05-05.
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