Method and power plant comprising a solid oxide fuel cell (SOFC) for production of electrical energy and H.SUB.2 .gas

Abstract

Method and power plant comprising a Solid Oxide Fuel Cell (SOFC) for production of electrical energy and H.sub.2 gas. The power plant is charged with a feed gas selected from the group consisting of natural gas, bio-gas and syngas. The feed gas, prior to being fed to the SOFC, is reformed in a reformer with a CaO containing CO.sub.2 absorber, thereby producing a carbon free H.sub.2 gas as feed for the SOFC while converting CaO to CaCO.sub.3. The latter is regenerated to CaO in an endothermic reaction in a CaO regenerator at a temperature of at least 850° C. utilizing heat from the SOFC to heat the regenerator. A heat exchange medium collects heat in the SOFC and is subjected to further temperature increase in a heating device before being subjected to heat exchange in the CaO regenerator.

Claims

1. A method for production of electrical energy and H.sub.2 gas in a power plant comprising a Solid Oxide Fuel Cell (SOFC) (30), comprising charging a feed gas (111) selected from the group consisting of natural gas, bio-gas and syngas, reforming said feed gas (111) with CaO containing CO.sub.2 absorber in a reformer (21) to thereby produce a carbon-free H.sub.2 gas (115, 116) while converting CaO to CaCO.sub.3, regenerating the CaCO.sub.3 to CaO in an endothermic reaction in a CaO regenerator (22) at a temperature of at least 850° C. utilizing heat from the SOFC (30) to heat the regenerator (22), feeding the carbon-free H.sub.2 gas to the SOFC (30), wherein at least one heat exchange medium (123, 201) collecting heat in the SOFC (30) is subjected to temperature increase in a heating device (41, 41′, 41″) prior to being subjected to heat exchange in the CaO regenerator (22), the at least one heat exchange medium (123, 201) is selected from the group consisting of exhaust gas (123) from the SOFC (30) and a dedicated heat exchange medium (201) circulating in a closed loop between the SOFC (30), the heating device (41, 41′, 41″) and the CaO regenerator (22), and the heating device (41, 41′, 41″) is charged with one of: (i) a gas having a biogenic origin, and (ii) a gas of fossil origin, wherein the gas is subjected to one of (a) being burned in pure oxygen to yield an exhaust gas of pure CO.sub.2, and (b) being burned in air yielding an exhaust gas that is subjected to a separate step of CO.sub.2 collection (128′).

2. The method as claimed in claim 1, wherein the heating device (41) is a burner charged with substantially pure H.sub.2 (122) as a fuel gas in an amount sufficient to increase the temperature of the exhaust gas (123) from the SOFC (30) by at least 50° C.

3. The method as claimed in claim 2, wherein at least a portion of the fuel gas charged to the heating device (41) is H.sub.2 gas deviated from the reformer (21).

4. The method as claimed in claim 3, wherein at least a portion of the fuel gas (122) charged to the heating device (41) is H.sub.2 gas deviated from the H.sub.2 discharge (119) of the SOFC (30).

5. The method as claimed in claim 2, wherein at least a portion of the fuel gas (122) charged to the heating device (41) is H.sub.2 gas deviated from the H.sub.2 discharge (119) of the SOFC (30).

6. The method as claimed in claim 1, wherein the exhaust gas (123) from the SOFC (30) is hot air of about 830° C.

7. The method as claimed in claim 1, comprising operating the heating device (41) so as the exhaust gas (126) leaving the heating device (41) has a temperature of at least 850° C.

8. The method as claimed in claim 7, wherein the heating device is operated so as the exhaust gas (126) leaving the heating device (41) has a temperature of at least 1000° C.

9. The method as claimed in claim 1, wherein the heat exchange medium (201) is a dedicated heat exchange medium (201) circulating in a closed loop between the SOFC (30), the heating device (41′, 41″) and the CaO regenerator (22).

10. The method as claimed in claim 1, wherein fuel to both the reformer and the heating device is of biogenic origin.

11. The method as claimed in claim 1, comprising switching between a first reformer for fuel with a first amount of initial CO.sub.2 and a second, larger reformer for fuel with a second, larger amount of initial CO.sub.2.

12. The method as claimed in claim 1, comprising heating air with exhaust from the heating device to provide heated air, and charging the heated air to the solid oxide fuel cell.

13. The method as claimed in claim 1, wherein the heating device is charged with the gas of fossil origin, which is burned in air yielding the exhaust gas that is subjected to the separate step of CO.sub.2 collection.

14. The method as claimed in claim 1, comprising heat exchanging a discharge flow from the solid oxide fuel cell with a charge flow of pure oxygen to the heating device, charging the heating device with the gas of fossil origin, and burning the gas in the pure oxygen to yield the exhaust gas of pure CO.sub.2.

15. A power plant for production of electrical energy and H.sub.2 gas, the power plant comprising a solid oxide fuel cell (SOFC) (30) and being arranged to receive a charge of a feed gas (111) selected from the group consisting of natural gas, bio-gas and syngas, comprising a reformer (21) for receiving the feed gas and reforming the feed gas with a CaO containing CO.sub.2 absorber to produce a carbon free H.sub.2 gas (115) to be fed to the SOFC (30) and converting CaO to CaCO.sub.3; a regenerator for converting the CaCO.sub.3 back to CaO at a temperature of at least 850° C., wherein a heating device (41, 41′, 41″) is connected between the SOFC (30) and the regenerator (22) and configured to allow a heat exchange medium (123, 201) collecting heat from the SOFC to be additionally heated therein and thereafter used for heat exchange in the regenerator (22), and the heat exchange medium (123, 201) is selected from the group consisting of exhaust gas (123) from the SOFC (30) and a dedicated heat exchange medium (201) circulating in a closed loop between the SOFC (30), the heating device (41, 41′, 41″) and the CaO regenerator (22), and the heating device (41, 41′, 41″) is charged with one of: (i) a gas having a biogenic origin, and (ii) a gas of fossil origin, wherein the gas is subjected to one of (a) being burned in pure oxygen to yield an exhaust gas of pure CO.sub.2, and (b) being burned in air to yield an exhaust gas that is thereafter subjected to a separate step of CO.sub.2 collection (128′).

16. The power plant as claimed in claim 15, wherein a closed loop is arranged to circulate a dedicated heat exchange medium (201) between the SOFC (30), the heating device (41, 41′, 41″) and the CaO regenerator (22).

17. The power plant of claim 16, wherein a discharge flow (123′) from the solid oxide fuel cell (30) is heat exchanged with a charge flow of pure oxygen (125′) to the heating device (41″).

18. The power plant as claimed in claim 15, wherein the heating device 41 is charged with a fuel selected among fossil fuels and biofuels.

19. The power plant as claimed in claim 15, wherein oxygen required by the heating device (41′) is supplied by one or more selected from the group consisting of a separate air supply (125) and a discharge flow (123′) from the solid oxide fuel cell (30).

20. The power plant of claim 15, wherein a discharge flow (123′) from the solid oxide fuel cell (30) is heat exchanged with a charge flow of pure oxygen (125′) to the heating device (41″).

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Different embodiments of the invention are illustrated below with reference to the enclosed drawings, where;

(2) FIG. 1 is a schematic view of a disclosed first embodiment.

(3) FIG. 2 is a schematic view of a second disclosed embodiment.

(4) FIG. 3 is a schematic view of a third disclosed embodiment.

DETAILED DESCRIPTION

(5) Attention is drawn to FIG. 1, showing a hydrogen production plant where an SOFC system is combined with a fuel reformer, a CaO CO.sub.2-absorbent regenerator and an exhaust heating system 40 for enhancement of the temperature.

(6) A fuel flow 111 is charged to a Reformer unit 21 being part of a Ca-looping system 20, arranged to reform the fuel and to take care of initial CO.sub.2 (if needed) and CO.sub.2 released in the reforming process. The fuel is typically natural gas, other methane-rich gas, such as gas produced in fermentation units or syngas. A substantially pure hydrogen gas 115 leaves the reformer unit 21. In the reformer unit 21, the process of reforming involves a reaction between the fuel, water (steam) and CaO in which the latter is converted to CaCO.sub.3 in an exothermic reaction. The CaCO.sub.3 made both from the initial CO.sub.2 (if present) and from the reforming process is subsequently regenerated to CaO in an endothermic process to be described. Water 112 in vaporized form is also charged to the reformer unit 21.

(7) The substantially pure hydrogen gas 115 leaving the reformer unit 21 is heated in a first heat exchanger 51 before being charged to a solid oxide fuel cell (SOFC) 30, as a heated hydrogen flow 116. The SOFC produces electricity and releasing varying amounts of hydrogen 119. Air 118 is also charged to the SOFC, typically after having been heated in a second heat exchanger 52.

(8) The exhaust gas 123 from the SOFC 30 is substantially pure air due to the fact that the fuel 116 charged to the fuel cell is substantially pure hydrogen. The temperature of the exhaust gas from the SOFC 30 is typically about 830° C. and may be somewhat less.

(9) As indicated above, the CaCO.sub.3 generated in the reformer unit 21 needs to be regenerated to CaO for reuse as capturing agent in the reformer. This takes place in a regenerator 22 forming a second part of the Ca-looping system 20. However, the regeneration of CaCO.sub.3 needs a temperature of at least 850° C., more preferably at least 900° C. to operate efficiently and it is an endothermic process consuming energy. The regenerator 22 also needs some water 114 for its operation, said water typically being preheated in a third heat exchanger 53 in order not to act as a coolant.

(10) The exhaust gas 123 from the SOFC is a promising candidate for maintaining the temperature of the regenerator 22, but its temperature is typically not high enough to perform the task on its own. In practice, the temperature of the exhaust gas 123 is too low to effectively maintain a sufficient temperature in the regenerator 22 at which the CaCO.sub.3 is converted to CaO for further use. The core of the disclosed embodiments is the use of a dedicated system, integrated with a fuel reformer, a CaO CO.sub.2-absorbent regenerator, and an exhaust temperature increasing system 40 arranged to elevate the temperature of the exhaust gas 123 to allow it to be used for the purpose of maintaining an effective temperature in the regenerator 22 by using a heating device 41 for enhancement of the temperature.

(11) FIG. 1 gives a schematic view of a hydrogen production plant, in which an SOFC system 30, is combined with a fuel reformer 21, a CaO CO.sub.2-absorbent regenerator 22 and an exhaust heating device 41, which is fueled for enhancement of the temperature. In this embodiment the fuel charged to the exhaust heating device 41 is burned in air 125.

(12) If all the fuel to both the Reformer 21, and the exhaust heating device 41 is of biogenic origin the total system would be climate neutral. Furthermore, if the fuel, for the heating system through 124, is derived from biological sources, these can typically be:

(13) a) Hydrogen from the SOFC system 122

(14) b) Landfill gas (with bio-CO.sub.2).

(15) c) Produced biogas, with or without CO.sub.2 separation.

(16) d) Syngas from any bio-source (solid, liquid or gas)

(17) e) Solid carbon-containing source

(18) The CO.sub.2 related to/released from these processes would be climate neutral and can after the heat transfer 25 to the Regenerator 22 be released to air as flow 128 without undesired climate consequences. Hydrogen, the most preferred fuel for the exhaust heating device, can be delivered from the downstream side of the reformer 21 through 115, or more preferred as flow 122 which constitutes part of the hydrogen discharge flow 119 from the SOFC, after having had its temperature reduced in a heat exchanger, such as first heat exchanger 51, used to heat the inlet flow 115 of hydrogen to the SOFC 30.

(19) It is, however, also possible to obtain a situation with no climate consequences if the fuel 111 charged to the Reformer 21 is of fossil origin and the fuel to the exhaust heating device 41 is of biogenic origin (see above). This is because the CO.sub.2 from the reforming process in the Reformer 21 is efficiently absorbed by the CaO absorbent, cf. reaction a) (SE-SMR) and reaction b) (SE-WGS), and can thus easily be collected 100% pure from the Regenerator 22 for storage or use as flows 129, 130.

(20) Attention is now directed to FIG. 2, showing a hydrogen production plant where an SOFC system is integrated with a fuel reformer, a CaO CO.sub.2-absorbent regenerator and to an exhaust heating device for enhancement of the temperature. In this embodiment the heat integration is provided with a closed heat loop 40′.

(21) Most of the components of FIG. 2 are the same as the ones in FIG. 1. The difference between FIG. 1 and FIG. 2 is mainly that the heat transfer between the SOFC 30 and the Regenerator 22, via the exhaust heating device 41′, is provided by a closed heat loop 201, 202, 203, 204.

(22) If all the fuel to both the Reformer and the exhaust heating device, in the embodiment illustrated in FIG. 2 is of biogenic origin the total system would also be climate neutral. Similar to the embodiment given in FIG. 1 it is in this case also possible to obtain a situation with no climate consequences if the fuel to the Reformer is of fossil origin and the fuel to the exhaust heating device is of biogenic origin (see above).

(23) If the fuel to the temperature heating device 41′ is derived from fossil sources, these can typically be:

(24) a) Hydrogen from the SOFC system

(25) b) Natural gas

(26) c) Gasified solid (coal), liquid or gas hydrocarbons (syngas).

(27) d) Coal

(28) This would for the carbon containing fuel require a separate CO.sub.2 collection system at 128′, to obtain a climate neutral situation.

(29) The heat transfers medium of the heat loop 201-204 in FIG. 2, can be different gases, such as for example; Hydrogen, CO.sub.2, air, helium, water vapor, different gas mixtures or fluids such as; mineral oils, hydrocarbons and different types of molten salts. The heat of the heat medium 201 leaving the SOFC system 30, is about 830° C. The heat of this heat loop is enhanced in the temperature heating device 41′ to at least 850° C., more preferable at least 950° C. and most preferred at least 1000° C., in order to meet the temperature regeneration requirement of the CaO absorbent in regenerator 22.

(30) The heated exhaust flow 123′ from the SOFC system 30 provides the oxygen for the heating process in 41′. The oxygen to the heating device may if needed also be provided by air inlet 125. The exhaust from 41′ is heat exchanged in second heat exchanger 52 to heat the air at flow 117 through 118 into the SOFC 30, before leaving the system as flow 128′ for release to atmosphere. If the fuel for the heating device is mainly or solely hydrogen, there will be little or no CO.sub.2 in the exhaust gas at 128′. If the heating device 41′ is fed wholly or partially by a different fuel, though a fuel of organic, non-fossil, origin, the exhaust gas at 128′ will be climate-neutral.

(31) The regeneration of the absorbent also releases substantial amounts of pure CO.sub.2 shown as flow 129, which needs to be taken care of (used or stored) preferably after having been used for heat exchange in a third heat exchanger 53.

(32) As shown in FIGS. 1 and 2, water (vapor) 112 is added to the reformer unit 21 in order to furnish the reaction zone with required amounts of oxygen and hydrogen.

(33) The principle illustrated by FIGS. 1 and 2 is generally that heat produced by the SOFC 30 is used to regenerate the absorber used to absorb CO.sub.2 in the process of reforming the feed gas, but since the temperature of the exhaust gas from the SOFC is typically a little too low to be used alone, its energy and temperature is increased in a subtle and efficient manner. Most elegant is perhaps the present process when hydrogen already being part of the system, is used for boosting the energy, then without the formation of any additional CO.sub.2.

(34) Attention is now directed to FIG. 3 showing a hydrogen production plant where an SOFC system is combined with a fuel reformer, a CaO CO.sub.2-absorbent regenerator and an exhaust heating device for enhancement of the temperature. In this embodiment the heat transfer is provided with a closed heat loop. The fuel (if carbon containing) to the exhaust heating device is burned in pure oxygen provided by an oxygen pump.

(35) Most of the components of FIG. 3 are the same as the ones in FIGS. 1 and 2. FIG. 3 shows an embodiment where the fuel to the Reformer 22, as well as to the exhaust heating device 41″, can be of fossil origin (CH.sub.4, natural gas syngas etc.), where it is possible to capture all CO.sub.2 from the total production system, for storage or use. The fuel to the heating device, would then have to be burned in pure oxygen supplied as flow 125′, by an oxygen pump. The oxygen 125′ is typically preheated in a fourth heat exchanger 54, with SOFC exhaust air 123′ from second heat exchanger 52. (It is to be noted that the heat exchanger 52 shown to heat flow 117 in FIGS. 1, 2, and 3 is the same heat exchanger as used to cool flow 127 (FIG. 1), flow 128′ (FIG. 2) and flow 123′ (FIG. 3)).

(36) It is worth noticing, though, that all heat exchange in the present disclosure which is not directly related to the enhancement of the temperature of the heat exchange medium to the CaO regenerator is optional and may be conducted in a number of different ways.

(37) While the inventive concepts disclosed herein may have the form of a number of different embodiments, the heat exchange medium the SOFC 30 typically comprises at least one of exhaust gas 123 and a dedicated heat exchange medium 201, the latter in case circulating in a closed loop between the SOFC, the heating device 41, 41′, 41″ and the CaO regenerator 22.

(38) The heating device 41 is in one preferred embodiment a burner charged with substantially pure hydrogen gas 122 in an amount sufficient to increase the temperature of the exhaust gas 123 from the SOFC 30 by at least 50° C.

(39) At least a part of the fuel gas charged to the heating device 41 is typically hydrogen gas deviated from the reformer 21.

(40) In one preferred embodiment, at least part of the fuel gas charged to the heating device 41 is hydrogen gas deviated from the hydrogen discharge 119 of the SOFC 30.

LIST OF REFERENCES

(41) 20 Ca-looping system 21 Reformer of Ca-looping system 20 22 Regenerator of Ca-looping system 20 25 heat exchanger in regenerator 22 30 SOFC 35 heat exchanger in SOFC 30 40 heat enhancement system (first version) 40′ heat enhancement system (2.sup.nd version) 40″ heat enhancement system (3.sup.rd version) 41 heating device (first version) 41′ heating device (second version) 41″ heating device (third version) 45 heat exchanger in heating device 41′ and 41″ 51 First heat exchanger 52 Second heat exchanger 53 Third heat exchanger 54 Fourth heat exchanger 111 Feed flow to 21 112 Water to reformer 113 water to (third) heat exchanger 114 water to regenerator 115 hydrogen from reformer 116 hydrogen from heat exchanger to SOFC 30 117 Air to heat exchanger (and later to SOFC) 118 Air from heat exchanger 52 to SOFC 30 119 hydrogen from SOFC to heat exchanger 51 120 hydrogen from heat exchanger 51 121 hydrogen substream for delivery, partial flow of 120 122 hydrogen substream for fuel to heating device 41 123 exhaust flow from SOFC 123′ exhaust flow from SOFC (alternative FIG. 2) 123″ 124 ext. fuel to heating device 41 125 air flow to heating device 41 125′ pure oxygen to heating device 41 126 exhaust flow from heating device 41 127 exhaust flow from heat exchange in regenerator 128 exhaust flow from heat exchanger 52 to atmosphere (FIG. 1) 128′ exhaust flow from heating device 41′ (FIG. 2) 128″ exhaust flow from heating device 41″ (FIG. 3) 128″′ exhaust flow from heat exchanger 54 (FIG. 3) 129 pure CO2 from regenerator 130 Pure CO2 from heat exchanger 53 201 heat exchange medium from SOFC 30 to heating device 41″ 202 heat exchange medium from heating device 41″ to regenerator 22 203 heat exchange medium from regenerator 22 to cooler 50 204 heat exchange medium from cooler 50 to SOFC 30