Amine gas treating, also known as amine scrubbing, gas sweetening and acid gas removal, refers to a group of processes that use aqueous solutions of various alkylamines (commonly referred to simply as ) to remove hydrogen sulfide (H2S) and carbon dioxide (CO2) from gases.
Processes within oil refineries or chemical processing plants that remove hydrogen sulfide are referred to as "sweetening" processes because the odor of the processed products is improved by the absence of "sour" hydrogen sulfide. An alternative to the use of amines involves membrane technology. However, membrane separation is less attractive due to the relatively high capital and operating costs as well as other technical factors.
Many different amines are used in gas treating:
The most commonly used amines in industrial plants are the alkanolamines DEA, MEA, and MDEA. These amines are also used in many oil refineries to remove from liquid hydrocarbons such as liquified petroleum gas (LPG).
The chemistry involved in the amine treating of such gases varies somewhat with the particular amine being used. For one of the more common amines, monoethanolamine (MEA) denoted as RNH2, the acid-base reaction involving the protonation of the amine electron pair to form a positively charged ammonium group (RNH) can be expressed as:
The resulting dissociated and ionized species being more soluble in solution are trapped, or scrubbed, by the amine solution and so easily removed from the gas phase. At the outlet of the amine scrubber, the sweetened gas is thus depleted in and .
A typical amine gas treating process (the Girbotol process, as shown in the flow diagram below) includes an absorber unit and a regenerator unit as well as accessory equipment. In the absorber, the downflowing amine solution absorbs and reacts with and from the upflowing sour gas to produce a sweetened gas stream (i.e., a gas free of hydrogen sulfide and carbon dioxide) as a product and an amine solution rich in the absorbed acid gases. The resultant "rich" amine is then routed into the regenerator (a stripper with a reboiler) to produce regenerated or "lean" amine that is recycled for reuse in the absorber. The stripped overhead gas from the regenerator is concentrated and .
The choice of amine concentration in the circulating aqueous solution depends upon several factors, involving the composition of the feed gas natural gas or petroleum refinery by-product gases that contain relatively low concentrations of both H2S and CO2 or whether the unit is treating gases with a high percentage of CO2 such as the offgas from the steam reforming process used in ammonia production or the from power plants.
Both H2S and CO2 are acid gases and hence corrosive to unprotected carbon steel. Their corrosiveness are greatly enhanced in the presence of moisture. However, in an amine treating unit, CO2 is a stronger acid than H2S. Furthermore hydrogen sulfide can form a passivating film of iron sulfide that may act to protect the steel. When treating gases with a high percentage of CO2, control of the CO2 loading in the amine is important to protect carbon steel from corrosion. Higher amine concentrations will have lower loading compared to lower concentrations at the same circulation rate.
Another factor involved in choosing the amine concentration is the relative solubility of H2S and CO2 in the selected amine. The choice of the type of amine will affect the required circulation rate of amine solution, the energy consumption for the regeneration and the ability to selectively remove either H2S alone or CO2 alone if desired. For more information about selecting the amine concentration, the reader is referred to Kohl and Nielsen's book.
In the specific case of the industrial synthesis of ammonia, for the steam reforming process of hydrocarbons to produce gaseous hydrogen, amine treating is one of the commonly used processes for removing excess carbon dioxide in the final purification of the gaseous hydrogen.
In the biogas production it is sometimes necessary to remove carbon dioxide from the biogas to make it comparable with natural gas. The removal of the sometimes high content of hydrogen sulfide is necessary to prevent corrosion of metallic parts after burning the bio gas.
There are multiple classifications of amines, each of which has different characteristics relevant to CO2 capture. For example, monoethanolamine (MEA) reacts strongly with CO2 and has a fast reaction time and an ability to remove high percentages of CO2, even at low CO2 concentrations. Typically, monoethanolamine (MEA) can capture 85% to 90% of the CO2 from the flue gas of a coal-fired plant, which is one of the most effective solvent to capture CO2.
Challenges of carbon capture using amine include:
The partial pressure is the driving force to transfer CO2 into the liquid phase. Under low pressure, this transfer is hard to achieve without increasing the reboilers' heat duty, which will result in higher costs.
Primary and secondary amines, for example, MEA and DEA, will react with CO2 and form degradation products. O2 from the inlet gas will cause degradation as well. The degraded amine is no longer able to capture CO2, which decreases the overall carbon capture efficiency.
Currently, a variety of amine mixtures are being synthesized and tested to achieve a more desirable set of overall properties for use in CO2 capture systems. One major focus is on lowering the energy required for solvent regeneration, which has a major impact on process costs. However, there are trade-offs to consider. For example, the energy required for regeneration is typically related to the driving forces for achieving high capture capacities. Thus, reducing the regeneration energy can lower the driving force and thereby increase the amount of solvent and size of absorber needed to capture a given amount of CO2, thus, increasing the capital cost.
MEA and DEA
Other amines
Uses
Carbon capture and storage
See also
External links
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