This application is a 371 of International Patent Application No. PCT/EP2013/072433, filed Oct. 25, 2013, which claims foreign priority benefit under 35 U.S.C. §119 of German Patent Application No. 10 2012 110 520.0, filed Nov. 2, 2012, the disclosures of which patent applications are incorporated herein by reference.
This invention relates to a process for producing dry synthetic natural gas (SNG, Synthetic Natural Gas) from solid or liquid, carbonaceous fuel.
Such processes are known. In essence, they consist of the following process steps:
As solid carbonaceous fuel lignite or hard coal, as liquid fuel heavy oil or tar frequently is used.
A widely used method for gasifying coal for example is the fixed-bed pressure gasification method, cf. Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed., Vol. 15, Gas Production, Chap. 4.4.
The principle of process stage b), cooling of the gas and separation of the gas condensate, is described in the patent specification DE 2 542 055 C3.
Known methods for gasifying heavy oil are described in Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed., Vol. 15, Gas Production, Chap. 3.2.
In the raw gas conversion according to process step c), carbon monoxide is converted into carbon dioxide and hydrogen by adding steam to the gas, catalytically supported, to an extent as it is required for the succeeding process step e), cf. Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed., Vol. 15, Gas Production, Chap. 5.1.2 Raw Gas Shift Catalyst and Ullmanns Encyklopädie der technischen Chemie, 4th Ed., Vol. 14, Kohle, Gaserzeugung, Chap. 5.1.4.
A widely used process according to process step d) is the so-called Rectisol® process, cf. Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed.,Vol. 15, Gas Production, Chap. 5.4.2.1. The methanol used for gas washing is circulated via a regeneration plant. The regeneration plant also comprises a methanol-water separation column.
The catalytically supported conversion of the carbon monoxide and dioxide contained in the gas and of hydrogen to synthetic natural gas according to process step e), which also is referred to as methanation, can be effected with a process which comprises a cascade of e.g. three reactors which each are filled with a fixed bed of a methanation catalyst and which one after the other are traversed by the gas. The carbon monoxide and dioxide contained in the synthesis gas is converted into methane and steam by using hydrogen. The principle of the methanation is described e.g. in Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed., Vol. 15, Gas Production, Chap. 5.3.
In process step f), the steam for the most part is condensed out by cooling the gas to a temperature above 0° C. by means of cooling or cold water.
The residual moisture content is removed from the gas by drying processes according to process step g). The principle of this process, applied to natural gas, is described in Ullmanns Encyklopädie der technischen Chemie, 4th Ed., Vol. 10, Erdgas, Aufbereitung, Chap. 2.2. These processes equally can be applied both for natural and for synthetic natural gas.
In this process it is disadvantageous that in process step g) a regeneration of the glycol laden with moisture or of the molecular sieve is necessary. In addition, there is each obtained a gas stream laden with hydrocarbons, which, since a separation or combustion of the hydrocarbons would be uneconomic, in many cases is disposed of into the environment untreated or is supplied to a possibly present torch system.
It is the object of the invention to provide a process which avoids the disadvantages of the prior art. This object is solved by a process according to the features of claim 1.
According to the invention, the prior art processes for removing the residual moisture by a condensation of the moisture at a low temperature corresponding to the targeted dew point, which are mentioned in process step g), are replaced. After having been predried in process step f) by condensing out the moisture by means of cooling and/or cold water, the gas is mixed with methanol, so that methanol is present in the gas in the form of vapor or aerosol. For this purpose, the methanol preferably is brought in contact with the gas by injection or spraying in. The gas then is passed through a condenser, wherein it is cooled to the desired dew point of below 0° C. The water condensed out along with the methanol distributed in the gas forms a liquid water-methanol solution. The formation of a water ice layer on the heat exchanger surface of the condenser is avoided in this way.
The water-methanol solution is separated from the gas and the gas is heated to the desired discharge temperature, so that dried synthetic natural gas is obtained. In the process according to the invention it is advantageous that with the exception of methanol, which anyway is present due to its use in process step d), no further auxiliary substances foreign to the process, such as glycol or adsorbents, are required. The logistic expenditure for handling and keeping these auxiliary substances in stock therefore can be omitted.
In an advantageous aspect of the invention the water-methanol solution separated from the water is charged for processing into the methanol-water separation column of the regeneration means of process step d). Due to the utilization of the separating apparatus present already, a particularly efficient procedure is obtained.
With the invention, an economic and environmentally friendly process thus is provided for the treatment of raw gas produced by pressure gasification of solid, carbonaceous feedstocks, which provides for a higher energy efficiency with regard to the thermal energy contained in the raw gas and in the gas condensate.
Number | Date | Country | Kind |
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10 2012 110 520 | Nov 2012 | DE | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2013/072433 | 10/25/2013 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2014/067877 | 5/8/2014 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
4031030 | Rudolph | Jun 1977 | A |
4979966 | Rojey et al. | Dec 1990 | A |
5392594 | Moore | Feb 1995 | A |
5670027 | Paradowski | Sep 1997 | A |
20100163803 | Klein | Jul 2010 | A1 |
20120214881 | Wahlstrom | Aug 2012 | A1 |
20120297822 | Bailey | Nov 2012 | A1 |
Number | Date | Country |
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2 542 055 | Mar 1977 | DE |
2011 154535 | Dec 2011 | WO |
Entry |
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Ullmann's Encyclopedia of Industrial Chemistry, 6th Ed., vol. 16, Gas Production, 2012, 483-539. |
Number | Date | Country | |
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20150299597 A1 | Oct 2015 | US |