Читать книгу Encyclopedia of Renewable Energy - James Speight G., James G. Speight - Страница 25

The primary process for sweetening sour gas streams is similar to the processes of glycol dehydration and removal of gas stream liquids by absorption. In this case, however, amine (olamine) solutions are used to remove the hydrogen sulfide (the amine process). The sour gas is run through a tower, which contains the olamine solution.

There are two principle amine solutions used, monoethanolamine (MEA) and diethanolamine (DEA). Either of these compounds, in liquid form, will absorb sulfur compounds from the gas stream as it passes through. The effluent gas is virtually free of sulfur compounds, and thus loses its sour gas status; the amine solution used can be regenerated for reuse.

Although most sour gas sweetening involves the amine absorption process, it is also possible to use solid desiccants like iron sponge to remove hydrogen sulfide and carbon dioxide. Treatment of gas to remove the acid gas constituents (hydrogen sulfide and carbon dioxide) is most often accomplished by contact of the gas stream with an alkaline solution. The most commonly used treating solutions are aqueous solutions of the ethanolamine or alkali carbonates.

A considerable number of other treating agents have been developed in recent years. Most of these newer treating agents rely upon physical absorption and chemical reaction. When only carbon dioxide is to be removed in large quantities or when only partial removal is necessary, a hot carbonate solution or one of the physical solvents is the most economical selection.

The most well-known hydrogen sulfide removal process is based on the reaction of hydrogen sulfide with iron oxide (often also called the iron sponge process or the dry box method) in which the gas is passed through a bed of wood chips impregnated with iron oxide.

The iron oxide process is the oldest and still the most widely used batch process for sweetening gas streams and separation the gas liquids. The process was implemented during the 19th century. In the process, the sour gas is passed down through the bed. In the case where continuous regeneration is to be utilized a small concentration of air is added to the sour gas before it is processed. This air serves to continuously regenerate the iron oxide, which has reacted with hydrogen sulfide, which serves to extend the on-stream life of a given tower but probably serves to decrease the total amount of sulfur that a given weight of bed will remove.

The process is usually best applied to gases containing low to medium concentrations (300 ppm) of hydrogen sulfide or mercaptans. This process tends to be highly selective and does not normally remove significant quantities of carbon dioxide. As a result, the hydrogen sulfide stream from the process is high purity. The use of iron sponge process for sweetening sour gas is based on adsorption of the acid gases on the surface of the solid sweetening agent followed by chemical reaction of ferric oxide (Fe2O3) with hydrogen sulfide:

The reaction requires the presence of slightly alkaline water and a temperature below 43°C (110°F) and bed alkalinity (pH = 8 to 10) should be checked regularly, usually on a daily basis. The pH level is be maintained through the injection of caustic soda with the water. If the gas does not contain sufficient water vapor, water may need to be injected into the inlet gas stream.

The ferric sulfide produced by the reaction of hydrogen sulfide with ferric oxide can be oxidized with air to produce sulfur and regenerate the ferric oxide:

The regeneration step is exothermic and air must be introduced slowly so the heat of reaction can be dissipated. If air is introduced quickly the heat of reaction may ignite the bed. Some of the elemental sulfur produced in the regeneration step remains in the bed. After several cycles, this sulfur will form a cake over the ferric oxide, decreasing the reactivity of the bed. Typically, after 10 cycles the bed must be removed and a new bed introduced into the vessel.

The iron oxide process is one of several metal oxide-based processes that scavenge hydrogen sulfide and organic sulfur compounds (mercaptans) from gas streams through reactions with the solid based chemical adsorbent. They are typically non-regenerable, although some are partially regenerable, losing activity upon each regeneration cycle. Most of the processes are governed by the reaction of a metal oxide with hydrogen sulfide to form the metal sulfide. For regeneration, the metal oxide is reacted with oxygen to produce elemental sulfur and the regenerated metal oxide. In addition, to iron oxide, the primary metal oxide used for dry sorption processes is zinc oxide.

In the zinc oxide process, the zinc oxide media particles are extruded cylinders 3-4 mm in diameter and 4-8 mm in length and react readily with the hydrogen sulfide:

At increased temperatures (205 to 370°C, 400 to 700°F), zinc oxide has a rapid reaction rate, therefore providing a short mass transfer zone, resulting in a short length of unused bed and improved efficiency.

Removal of larger amounts of hydrogen sulfide from gas streams requires a continuous process, such as the Ferrox process or the Stretford process.

The Ferrox process is based on the same chemistry as the iron oxide process except that it is fluid and continuous. The Stretford process employs a solution containing vanadium salts and anthraquinone disulfonic acid. Most hydrogen sulfide removal processes return the hydrogen sulfide unchanged, but if the quantity involved does not justify installation of a sulfur recovery plant (usually a Claus plant), it is necessary to select a process that directly produces elemental sulfur.

The processes using ethanolamine and potassium phosphate are now widely used. The ethanolamine process, known as the Girbotol process, removes acid gases (hydrogen sulfide and carbon dioxide) from liquid hydrocarbons as well as from natural and from refinery gases. The Girbotol process uses an aqueous solution of ethanolamine (H₂NCH₂CH₂OH) that reacts with hydrogen sulfide at low temperatures and releases hydrogen sulfide at high temperatures. The ethanolamine solution fills a tower called an absorber through which the sour gas is bubbled. Purified gas leaves the top of the tower, and the ethanolamine solution leaves the bottom of the tower with the absorbed acid gases. The ethanolamine solution enters a reactivator tower where heat drives the acid gases from the solution. Ethanolamine solution, restored to its original condition, leaves the bottom of the reactivator tower to go to the top of the absorber tower, and acid gases are released from the top of the reactivator.

The process using potassium phosphate is known as phosphate desulfurization, and it is used in the same way as the Girbotol process to remove acid gases from liquid hydrocarbons as well as from gas streams. The treatment solution is a water solution of potassium phosphate (K₃PO₄), which is circulated through an absorber tower and a reactivator tower in much the same way as the ethanolamine is circulated in the Girbotol process; the solution is regenerated thermally.

Moisture may be removed from hydrocarbon gases at the same time as hydrogen sulfide is removed. Moisture removal is necessary to prevent harm to anhydrous catalysts and to prevent the formation of hydrocarbon hydrates (such as C₃H₈.18H₂O) at low temperatures. A widely used dehydration and desulfurization process is the glycolamine process, in which the treatment solution is a mixture of ethanolamine and a large amount of glycol. The mixture is circulated through an absorber and a reactivator in the same way as ethanolamine is circulated in the Girbotol process. The glycol absorbs moisture from the hydrocarbon gas passing up the absorber; the ethanolamine absorbs hydrogen sulfide and carbon dioxide. The treated gas leaves the top of the absorber; the spent ethanolamine-glycol mixture enters the reactivator tower, where heat drives off the absorbed acid gases and water.

Other processes include the Alkazid process for removal of hydrogen sulfide and carbon dioxide using concentrated aqueous solutions of amino acids. The hot potassium carbonate process decreases the acid content of natural and refinery gas from as much as 50% to as low as 0.5% and operates in a unit similar to that used for amine treating. The Giammarco-Vetrocoke process is used for hydrogen sulfide and/or carbon dioxide removal. In the hydrogen sulfide removal section, the reagent consists of sodium or potassium carbonates containing a mixture of arsenite derivatives (such as sodium arsenite, NaAsO₂) and arsenate derivatives (such as sodium arsenate, Na₃AsO₄); the carbon dioxide removal section utilizes hot aqueous alkali carbonate solution activated by arsenic trioxide or selenous acid or tellurous acid.

Molecular sieves are highly selective for the removal of hydrogen sulfide (as well as other sulfur compounds) from gas streams and over continuously high absorption efficiency. They are also an effective means of water removal and thus offer a process for the simultaneous dehydration and desulfurization of gas. Gas that has excessively high water content may require upstream dehydration, however.

The molecular sieve process is similar to the iron oxide process. Regeneration of the bed is achieved by passing heated clean gas over the bed. As the temperature of the bed increases, it releases the adsorbed hydrogen sulfide into the regeneration gas stream. The sour effluent regeneration gas is sent to a flare stack, and up to 2% of the gas seated can be lost in the regeneration process. A portion of the gas stream may also be lost by the adsorption of hydrocarbon components by the sieve.

See also: Alkazid Process, Gas Cleaning, Gas Processing, Gas Treating.