(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (10) International Publication Number (19) World Intellectual Property Organization International Bureau. (43) International Publication Date 9 September 2011 (09.09.2011) WO 2011/107279 Al (61) nernationa Patent Classifica (81) Designated Stats fanless otherwise indicated, for every HOIM $106 200501) BOIS 19724 200601) kindof national protection available): AP, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, @1)_ International Application Number: CA, CH, CL; CN, CO, CR, CU. CZ, DE, DK, DM, DO, PCT/EP2011/001046 DZ, BC, FE, EG, BS, Fl, GB, GD, GE, GH, GM, Gi (22) International Filing Date: HIN, HR, HU, ID, IL, IN, 1S, JP, KE, KG, KM, KN, KP, 2 March 2011 (02,03.2011) KR. KZ, LA. LC, LK, LR, LS, LT, LU, LY, MA, MD, ” ME, MG, MK, MN, MW, MX, MY, MZ, Na, NG, NI 25) Filing Language: English ‘NO, NZ, OM, PE, PG, PH, PL, PT, RO, RS, RU, SC, SD, (26) Publication Language: English SE, SGSK, SL, SM, ST, SV,'SY. TH, J, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, YN, ZA, ZM, ZW. 0) Priority Data: 61/309,542 2 March 2010(0203.2010) US. (#4) Designated States (uniess otherwise indicated, for every ind of regional protection available): ARIPO (BW, GH, (7D Applicant for all designated States except US): AM- GM, KE, LR LS, MW, MZ, NA, SD, SL, SZ, TZ. UG, MINEX A/S [DK/DK]; Gladsaxeve} 363, DK-2860 7M, ZW), Entasian (AM, AZ, BY. KG, KZ, MD, RU, TI, Soborg (DK), ‘TMD, Furopean (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EES, Fl, FR, GB, GR, HR, HU, Ie, IS, TT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE; Si, SK, SM, TR), OAPI (BF, BI, CF, CG, Cl, CM, GA, GN, GQ, GW, ML, MR, NE, SN, TD, TG), (2) Inventors; and (75) Inventors/Applicants (for US only): CHAKRABORTY, Debasish (BD/DK]; Oxiond Have 271, DK-2200 Copen= agen S. (DK), PETERSEN, Hearlkx Nybo [DK/DK], Lundiotieve) 84 B Tv, DK-2800 Kongens Lyngby (DK). Published JOHANNESSEN, ‘Tue [DK/DK]; Platanhaven 110, DK-2600 Glostrup (DK), (74) Agent: LIPPICH, Wolfgang; Samson & Parner, Wide mayerstrasse 5, 80538 Miichen (DE), — with international search report (drt 21(3)) (64) Title: APPARATUS FOR GENERATING HYDROGEN FROM AMMONIA STORED IN SOLID MATERIALS AND IN- TEGRATION THEREOF INTO LOW TEMPERATURE FUEL CELLS a0 / Cocke oe Smo ote o “mht ne one) cenpuston Fig. 2 (57) Abstract: An ammonia-based hydrogen generation reactor (110) comprises: an ammonia cracking chamber (1) with an am= ‘monia cracking catalyst an inner combustion chamber (2) with # combustion or oxidation catalyst being in thermal contact with the ammonia cracking chamber, an ammonia gas prebeating chamber (3), and an outer jacket annulus (6) for recovery of heat from the combustion products exiting the combustion chamber (2), wherein the cracking chamber (1), the inner combustion chamber 2), the preheating chamber (3) aud the heat recovery jacket annulus (6) are arranged concentrically. Furher described is a system for generating hydrogen comprising at least one ammonia storage unit (119, 120, 400) which, when in operation, is combined with at least one hydrogen generation reactor (110), wherein, when in operation, the waste heat ofthe atleast one hydrogen gener. ation eactor (110) is transferred to at least one storage unit (119, 120, 400) being in operation. A power generating device funber ‘comprising fne cell, and a method for operating the system for generating hydrogen are also described = a g a 8 2 S a 9 S10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 1 Apparatus for generating hydrogen from ammonia stored in solid materials and integration thereof into low temperature fuel cells FIELD OF THE INVENTION The invention relates to the energy efficient generation of hydrogen by cracking ammonia stored in a solid storage material, e.g. as metal ammine salts, and the generation of power using a low temperature fuel cell. BACKGROUND OF THE INVENTION Ammonia is a widely used chemical with many applications. One specific application is as fuel for fuel cells. Ammonia can be a zero-carbon fuel if the CO2 produced during the conventional production process is sequestered or if it can be synthesized using nuclear energy or renewable energy, e.g. wind (see e.g. United States Patent No. US 2008/0248353; and Chakraborty et al., Fuel Cells Bulletin, October 2009, both incorporated herein by reference in their entirety.) To be useful as a fuel for a low temperature fue! cell, ammonia needs to be cracked into hydrogen and nitrogen by passing it through a reactor. Ammonia cracking is an endothermic process requiring 46 kJ/mol of ammonia according to the following reaction: NH391.5 He + 0.5 Nz AHzs9 = 46 ku/mol NH Ammonia crackers for production of hydrogen for feeding fuel cells have been proposed e.g. in WO 2006/113451 A2, US Patent No. US 6,936,363 B2, US Patent No. US 7,267,779 B2 all incorporated herein by reference in their entirety. For most applications, and in particular in automotive applications, the storage of ammonia in the form of a pressurized liquid in a vessel is too hazardous. A storage method involving ad- or absorption in a solid can circumvent the safety hazard of anhydrous liquid ammonia,10 15 20 25 Wo 2011/107279 PCT/EP2011/001046 It is desirable to operate an ammonia cracker for production of hydrogen as. energy efficient as possible SUMMARY OF THE INVENTION In a first aspect the invention relates to an ammonia-based hydrogen generation reactor 110 comprising: - an ammonia cracking chamber 1 with an ammonia cracking catalyst, - an inner combustion chamber 2 with a combustion or oxidation catalyst being in thermal contact with the ammonia cracking chamber, - an ammonia gas preheating chamber 3, and - an outer jacket annulus 6 for recovery of heat from the combustion products exiting the combustion chamber 2, wherein the cracking chamber 1, the inner combustion chamber 2, the preheating chamber 3 and the heat recovery jacket annulus 6 are arranged concentrically in this order, the cracking chamber 1 forming the innermost chamber. The hydrogen generation reactor 110 may also comprise heat transfer fins 10 extending from the surface of the combustion chamber 2 into the cracking chamber 1, and flow distribution holes 5 enabling uniform feeding of ammonia to the cracking chamber 1 by flow through the flow distribution holes 5. In a second aspect, the invention relates to system for generating hydrogen comprising at least one storage unit 119, 120, 400 containing a solid ammonia storage material 7 capable of releasing ammonia by desorption, preferably a metal ammine salt, which, when in operation, is combined with at least one hydrogen generation reactor 110 of claim 1, wherein, when in operation, the waste heat of the at least one hydrogen generation reactor 110 is transferred to at least one storage unit 119, 120, 400 being in operation. A first preferred embodiment of the second aspect is a system wherein the at least one storage unit 119, 120 has a hollow concentric channel 8 extending partly or all10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 3 the way through the unit in which, when in operation, one of said at least one hydrogen generating reactor 110 is inserted. In the system of the first preferred embodiment, the solid ammonia storage material 7 in the storage unit 119, 102 may be used as a part of a thermal insulation between the hydrogen generation reactor 110 operated at a temperature higher than 300°C and the surroundings. Furthermore, in the system of the first preferred embodiment the storage unit 120 may have an annular chamber 9 at the outer side with an inlet and outlet for fluid functioning as a heat exchanger for providing heat to desorb ammonia In the system of the first preferred embodiment, optionally modified as described in the preceding paragraph, the storage unit 119, 120 may have a space 11 between the hydrogen generating reactor 110 and an inner wall of the storage unit 119, 420, when said hydrogen generating reactor 110 is inserted. The hydrogen generation reactor 110 may be operated at a temperature higher than 300°C, in which case the space 11 can be varied or the space 11 is filled with a fluid which can be changed, so as to control the heat transfer between the hydrogen generating reactor 110 and the storage unit 119, 120. Any of the above embodiments of the system of the second aspect of the invention may further comprise a start-up unit 170 to assist the heating up of the combustion chamber 2 of the hydrogen generation reactor 110, and a heat exchanger 160 to recover heat of vaporization of steam formed in the combustion chamber 2 and to mix the ammonia from the storage unit 119,120 and air for entry into the ‘combustion chamber 2. The system of any of the above embodiments of the system of the second aspect of the invention may comprise two modules each comprising one of said a least one storage unit 119, 120 having a hollow concentric channel 8 extending partly or10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 4 all the way through the unit in which, when in operation, one of said at least one hydrogen generating reactor 110 is inserted. Ina second preferred embodiment of the second aspect of the invention, the system comprises at least two storage units 400 and one well isolated hydrogen generation reactor 110 as a stand-alone unit from which the heat generated in the combustion chamber 2 can be provided to the at least two storage units 400 externally or can be provided to a heat exchanger zone that extends into the storage units 400 via valves which direct the combustions products sequentially to one of the at least two storage units 400 which is in operation In the above system of the second preferred embodiment of the second aspect of the invention, the heat of the combustion products may be delivered to the storage unit 400 via a heat exchanger 160 exchanging heat from the combustion products from the combustion chamber 2 and/or the crack products from cracking chamber 1 to a circulating liquid which delivers a part of the heat to at least one of the at least two storage units 400. A third aspect of the invention is a power generation device 60, 70 comprising an alkaline fuel cell 151 or a PEM fuel cell 152 provided with an absorber 153 for absorbing traces of ammonia and the system for generating hydrogen of the first preferred embodiment of the second aspect, in which system the solid ammonia storage material 7 in the storage unit 119, 102 is used as a part of a thermal insulation between the hydrogen generation reactor 110 operated at a temperature higher than 300°C and the surroundings, wherein hydrogen from said system is fed to the alkaline fuel cell 151 or to the absorber 153, and after the absorption of traces of ammonia in the absorber 153 to the PEM fuel cell 152. The power generation device of the third aspect of the invention may further comprise a pump 180 which enhances the flow of ammonia from the storage unit 119, 120 to the hydrogen generating reactor 110 when the desorption pressure from the solid storage material 7 in the storage unit 2 is lower than the pressure10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 5 level required to overcome :the pressure drop during flow of ammonia through the power generation device 60, 70. A further aspect of the invention is a power generating device 60, 70 comprising an alkaline fuel cell 151 or a PEM fuel cell 152 provided with at least one absorber 153 for absorbing traces of ammonia, the system for generating hydrogen of the second preferred embodiment of the second aspect of the invention from which hydrogen is fed to the alkaline fuel cell 151 or to the absorber 153 and, after the absorption of traces of ammonia in the at least one absorber 153, to the PEM fuel cell 152, and a pump 180 which enhances the flow of ammonia from the storage unit 400 to the hydrogen generating reactor 110 when the desorption pressure from the solid storage material 7 in the storage unit 2 is lower than the pressure level required to overcome the pressure drop during flow of ammonia through the power generation device 60, 70. In yet another aspect, the invention relates to a method for operating a system for generating hydrogen comprising at least one storage unit 119, 120, 400 containing a solid ammonia storage material 7 capable of releasing ammonia by desorption, preferably a metal ammine salt, wherein waste heat from the hydrogen generation reactor (110) is recovered and used to fully or partially deliver the heat of desorption of ammonia from the ammonia storage material 7 to the storage unit 2 The method may further include introducing fuel cell coolant fluid of a fuel cell to an outer jacket of the storage unit 2 through a tube and returning the coolant fluid after exchanging heat with the ammonia storage material 7. BRIEF DESCRIPTION OF THE DRAWINGS. Fig. 1 shows a schematic graph of an embodiment of a hydrogen generation reactor with inlets and outlets to the reactor in an embodiment to the present invention.10 16 20 25 30 Wo 2011/107279 PCT/EP2011/001046 6 Fig. 2 shows a schematic cross sectional view of an embodiment of hydrogen generation reactor, The arrows show possible flow directions in different chambers. Fig, 3 shows a schematic graph of a storage unit which could be used together with the hydrogen generation reactor of Fig. 1 or Fig. 2 in a system for generating hydrogen according to the invention. Fig. 4 shows a schematic graph of an embodiment of a storage unit with outer annulus which could be used together with the hydrogen generation reactor of Fig. 1 or Fig. 2 in a system for generating hydrogen according to the invention. Fig. 5 shows a perspective view illustrating an embodiment of the hydrogen generation reactor-storage unit system. The hydrogen generation reactor acts also as a heating means and the storage unit also provides means for insulating the hydrogen generation reactor. Fig. 6 shows a process flow diagram for an embodiment of a system comprising a storage unit and a hydrogen generation reactor. Fig. 7 shows a process flow diagram for an embodiment of a system comprising a storage unit and a hydrogen generation reactor for power generation by an alkaline fuel cell. Fig. 8 shows a process flow diagram for an embodiment of a system comprising a storage unit, a hydrogen generation reactor and an absorber purifying the cracked product from trace ammonia for power generation by a PEM fuel cell Fig, 9 shows a process flow diagram for an embodiment of a system comprising a storage unit, a hydrogen generation reactor cracking ammonia and two absorbers for continuous purification of the cracked product from trace ammonia for power generation by a PEM fuel cell10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 a Fig. 10 shows a process flow diagram for a system comprising two sets of an embodiment of a storage unit-hydrogen generation reactor system, and two absorbers for continuous power generation by a PEM fuel cell. Fig. 11 shows a process flow diagram schematically showing direct transfer of heat from the hydrogen generation reactor exhaust gas to the ammonia storage unit(s) Fig. 12 shows a process flow diagram schematically showing transfer of heat from the hydrogen generation reactor exhaust gases to the ammonia storage unit(s) via a heat carrying fluid. The heat from the hydrogen generation reactor exhaust gases is first transferred to a heat carrying liquid which in turn transfers the heat to the storage unit(s). DETAILED DESCRIPTION ‘The particulars shown herein are by way of example and for purposes of illustrative discussion of the embodiments of the present invention only and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the present invention. In this regard, no attempt is made to show structural details of the present invention in more detail than is necessary for the fundamental understanding of the present invention, the description taken with the drawings making apparent to those skilled in the art how the several forms of the present invention may be embodied in practice. The present invention aims at an ammonia cracker which may be interfaced with a Unit containing solid-state ammonia storage material in a user-friendly way, and an improvement of the energy efficiency of the system by utilizing waste heat from the cracker and waste heat from the fuel ceil as heat sources to release ammonia from the storage material.10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 8 As mentioned at the outset, ammonia cracking is an endothermic process requiring 46 kJ/mol of ammonia according to the following reaction: NH3>1.5 Hz + 0.5 Nz Hose = 46 kJ/mol NHs. Itis an equilibrium controlled reaction and to achieve close to full conversion high reaction temperature (550°C to 750°C) is necessary. Therefore the heat of the reaction is needed to be delivered at a very high temperature to achieve maximum conversion. This heat can be delivered either by electrical heating or combustion of fuels e.9, hydrogen. Electrical heating is not only expensive in term of overall efficiency; itis unavailable during start-up, if the system does not contain a battery. Therefore it is preferred that the heat will be provided by combustion of an appropriate fuel preferably, ammonia or hydrogen. It is always challenging to effectively insulate a very high temperature process. Therefore, to improve energy efficiency, it is required that the waste heat of combustion is recovered as much as possible to provide heat to some other process in the system. Fuel cells, depending on the operation efficiency, may also generate more than 40% of waste heat. For low temperature fuel cells (typically operating around 80°C), this heat is generated at rather low temperature (e.g. 80 °C), which is considered as low-quality heat. Therefore, with low temperature proton exchange membrane fuel cells (PEMFCs) this heat is generally dissipated in the ambient. This dissipation process itself represents a big loss of system efficiency, on top of which the dissipation process consumes power for operating fans or blowers. Metal ammine salts are ammonia absorbing and desorbing materials, which can be used as solid storage media for ammonia. Preferred metal ammine salts used in the present invention have the general formula M.(NHs)oXz, wherein M is one or more cations selected from alkali metals such as Li, Na, K or Cs, alkaline earth metals such as Mg, Ca, Sr or Ba, and/or transition metals such as V, Cr, Mn, Fe, Co, Ni, Cu, or Zn or combinations thereof, such as NaAl, KAI, K2Zn, CsCu, or K2Fe; X is one or more anions selected from fluoride, chloride, bromide, iodide,10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 9 nitrate, thiocyanate, sulphate, molybdate, and phosphate ions; a is the number of cations per salt molecule; z is the number of anions per salt molecule; and n is the coordination number of 2 to 12, preferably 6 to 8. The metal ammine salts which can be used in the present invention are more fully described in WO 2008/012903 A2 and WO 2006/081824, both incorporated herein by reference in their entirety. In US 2008/0248353, incorporated herein by reference in its entirety, the solid metal ammines are described as an ideal “hydrogen carrier” fuel for vehicular and stationary power systems because of its high hydrogen content and incorporated safety issues. For these reasons, metal ammine salts are the preferred solid ammonia storage materials in the present invention, Degassing of ammonia from solid ammonia storage materials, e.g. metal ammine salts, is a process that requires heat, see WO 1999/01205 A1, US 5,161,389 and WO 2006/012903 A2, all incorporated herein by reference in their entirety. There are different ways of providing heat to the storage material: heat can be delivered by external heating of the storage container (WO 1999/01205 A1) or placing the heating element inside (US 5,161,389 and WO 2006/012903 A2). However, for improved system efficiency, it is desirable that the cracker and the ammonia storage material unit are designed in such a way that over all heat loss from the system is reduced. Interestingly, it is possible to find metal ammine salts (e.g. Sr(NHs)sCh or Ca(NHs)sCla) that release a significant portion of the stored ammonia at the temperature range which the waste heat of PCMFCs has. Therefore, a unique opportunity exists to also use the fuel cell waste heat to improve the overall system efficiency even further. Accordingly, the invention relates to an energy efficient cracking of ammonia for hydrogen production from ammonia stored as solid ammonia storage material, Preferably as metal ammine salts, and integration of the system with low10 18 20 25 30 Wo 2011/107279 PCT/EP2011/001046 10 temperature fuel cells, e.g. PEM (polymer electrolyte membrane) or fuel cells of the alkaline type, for high efficiency power generation. In a first aspect the invention relates to an ammonia-based hydrogen generation reactor (hereinafter also referred to as "ammonia cracker" or "jacket-cracker" or simply "cracker") comprising of combustion chamber for ammonia and/or off-gas from the fuel cell anode, a cracking chamber, an ammonia preheating chamber, and a combustion gas heat recovery chamber. Alll the four chambers of the cracker are concentric with the combustion chamber in the middle. The cracking chamber surrounds the combustion chamber. The cracker may also comprise a plurality of axially connected metal sheets for better dissipation of heat from the combustor to the cracking conduit. Ammonia enters at one end of the preheating chamber and after having traveled through the length of the preheating chamber, enters the cracking chamber, usually through a multiple of entrance holes in an end cap of the cracking chamber. The combustion chamber may be extended through the end cap of the cracking chamber to lead the combustion exhaust through the jacket. The cracking chamber contains an ammonia cracking catalyst and the combustion chamber contains a combustion catalyst capable of combusting NH or H2. In another aspect the invention relates to a system for generating hydrogen comprising at least one storage unit 119, 120, 400 containing a solid ammonia storage material 7 capable of releasing ammonia by desorption, preferably a metal ammine salt, which, when in operation, is combined with a hydrogen generation reactor 110 of the fist aspect, wherein, when in operation, the thermal energy of the heat recovered from the combustion products, of the hydrogen of the ‘combustion chamber 2 of the hydrogen generation reactor 110 is transferred to at least one storage unit 119, 120, 400 being in operation. The system for generating hydrogen may, in a preferred embodiment, includes a storage unit (cartridge) containing, e.g. metal ammine salts, into which the jacket~10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 " cracker may be plugged, and into which or with which the jacket-cracker is plugged or interfaced, when the system is in operation. The hollow concentric channel in the middle of the cartridge may extend all the way through the cartridge or may only extend into the cartridge from one end or side and not penetrate all the way through The cartridge may contain a hollow chamber e.g. in the form of a jacket covering fully or partly the outer surface of the cartridge for waste fuel cell coolant fluid. Fluid interfaces of ammonia and coolant fluid from the fuel recovery from the cell can be established as mentioned below. Ammonia released from the storage unit may be provided to the cracker through a tube joining the cracker and the storage unit via e.g. a quick connect or similar interface for easy replacement of the storage unit The invention also relates to a method for recovering the waste heat from the jacket-cracker and using the heat to fully or partially deliver the heat of desorption for ammonia. The salts used to store ammonia have very low thermal conductivities (in the order of 10? WimK comparable to microporous high temperature insulation from Microtherm®). This property of the salts is utilized to use the salt layer as an insulator for the cracker which works at a very high temperature. The device for performing the method includes a cylindrically or similar three-dimensional shaped block of metal ammine salts in a container having a hollow concentric channel extending all the way through the container. The diameter of the hollow channel is at least wide enough to receive the cracker. The method may also comprise introducing ammonia released from the storage unit to the cracker through a tube joining the cracker and the storage unit via a quick connect coupling or similar interface for easy replacement of the storage unit,10 15 20 25 Wo 2011/107279 PCT/EP2011/001046 12 The invention also relates to a method for recovering the heat loss from the jacket-cracker and using the heat to fully or partially deliver the heat of desorption for ammonia from the ammonia storage material via an annular space surrounding the outer surface of the storage container for waste heat recovery from the fuel cell coolant, The method may also include introducing the fuel cell coolant fluid to an outer jacket of the storage unit through a tube which may be connected to the outer Jacket via a quick connect and to return the coolant fluid after exchanging heat with the storage material e.g. through a tube. DESCRIPTION OF EMBODIMENTS Hereinafter, embodiments of the jacket-cracker and the storage unit and their use in a solid ammonia based power generating system will be described in detail Fig. 1 is a schematic of the jacket-cracker 110. Ammonia and/or hydrogen (not shown in Fig. 1) is mixed with air and the mixed gas enters the combustion chamber 2 which is connected to a combustion exhaust, as shown in Fig. 1 . Hydrogen could come from a fuel cell anode exhaust. Ammonia for cracking enters the reactor 110 through the preheating chamber 3. Fig. 2 indicates ammonia flow distribution holes 5 through which preheated ammonia enters into the cracking chamber 1. Also shown are heat transfer fins 10 attached to the outer wall of the combustion chamber 2 and extending into the cracking chamber 1 for better heat distribution for the endothermic cracking of ammonia. The exhaust gas of the combustion chamber 2 passes through the outermost annulus 6 before leaving the jacket-cracker 110 through one or more outlets, The cracking chamber exhaust gas which is a mixture of Hz, Nz and NHs of different concentrations depending on the operating point of the jacket-cracker, leaves the cracking chamber 1 through one or more outlets. All the inlets and outlets of the jacket-cracker are situated at the same end of the jacket-cracker ensuring countercurrent gas flow in each chamber. The combustion chamber can10 15 20 30 Wo 2011/107279 PCT/EP2011/001046 13 contain any ammonia combustion or oxidation catalyst e.g. 0.5% Pt on 3 mm. alumina pellets from Johnson Matthey. The cracking chamber can contain any ammonia cracking catalyst e.g. commercially available 2% Ru on 3 mm alumina pellets from Johnson Matthey. Now the ammonia storage units 119, 120 will be described. As shown in Fig. 3, the storage unit 119 includes a cylinder with a hollow concentric channel 8 all the way through the unit. The diameter of 8 is large enough to insert the jacket-cracker 110. The ammonia containing metal ammine salt in space 7 surrounds the channel 8. A similar container 120 is shown in Fig. 4, with the difference that this container has an annular space 9 surrounding the main storage chamber containing the meal ammine salt 7. Fig. 5 shows how the cracker can be interfaced with the storage unit 119 or 120, The space or gap 11 between the cracker 110 and the inner wall of the of the storage unit 119, 120 can be adjusted to control the heat transfer from the cracker to the storage unit and in turn control or influence the ammonia desorption rate. An insulating or a conducting material can also be used to fill up the space in order to decrease or increase the heat transfer from the cracker to the storage unit, respectively. An exemplary solid-ammonia based mobile hydrogen generation apparatus 50 shown in Fig. 6 includes an ammonia storage unit 120, a cracker 110, a heat exchanger 160, a start-up unit 170, a vacuum pump 180, and a battery (not shown). The cracker 110 is plugged into the storage unit 120. The startup unit 170 is needed only during the first few minutes to get the combustion chamber 2 ready for combustion of ammonia. To our knowledge, no catalyst exists to combust ammonia at room temperature, so the catalyst bed in the combustion chamber 2 of cracker 110 needs to be heated up for ammonia combustion. The start-up unit 170 comprises a heating rod inserted into a catalyst bed filled with ammonia cracking catalyst. Fed with ammonia, this unit produces a mixture of Hz, No, and ammonia which is transported through tube 260 and mixed with air introduced through tube 220. An air pump (not shown) can be used to deliver air. During start-up, vacuum10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 14 pump 180 pulls ammonia from the storage unit 120 when the temperature has not reached a level where a suitable desorption pressure above atmospheric level has been reached. The mixture is then forced to the combustion chamber 2 of the cracker 110 through heat exchanger 160 where it is preheated by exchanging heat with the combustor exhaust gas flowing to the heat exchanger 160 through tube 230. The heat exchanger 160 is used mainly to transfer the heat of vaporization of the steam (water vapor) exiting he combusting chamber 2 to the inlet fuel/air mixture. The channels of heat exchanger 160 are also used as mixing chambers for air and combustion fuel. The combustion exhaust gas leaves the heat exchanger 160 through tube 297. As soon as the combustion chamber 2 is ready for ammonia combustion, the ammonia flow from storage unit 120 is switched through tube 210 to mix with air and then taken through the heat exchanger 160 to the combustion chamber 2. The cracking chamber 1 in cracker 110, which is in thermal contact with the combustion chamber 2 , is heated up to the temperature required for cracking. Depending on the required purity of the H (in terms of slip ammonia concentration), the temperature can be selected, but typically this temperature will be between 300°C to 700°C. The ammonia for cracking enters the cracking chamber 1 through tube 200. Once the cracker 110 is heated up, waste heat is transferred to the surrounding storage unit 120 to provide the heat for desorption of ammonia, The cracked product, a mixture of Hz, N2 and ammonia leaves the cracker 110 through outlet tube 240. If Nz and ammonia-free pure Hp is needed, a palladium membrane can optionally be fitted into the exhaust line. In another embodiment of the invention, a power generator 60 with an alkaline type fuel cell 151 is used. The apparatus 60 shown in Fig. 7 uses the same hydrogen generation system 50 shown in Fig. 6. In order to utilize the waste heat from the fuel cell 151, the fuel cell stack coolant fluid is passed via tube 270 through the outer chamber 9 of the storage unit 120 for exchanging heat to the storage material 7. The outlet from the storage unit 2 can be passed through a radiator via tube 280, if more heat removal is needed by the coolant or directly to the fuel cell by-passing the radiator via tube 290. The fuel cell anode exhaust gas which contains unconverted Hz can be transported to the combustion chamber 2 of the cracker 110 via tube 300 to combust the hydrogen in the stream10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 15 Another embodiment of the invention is a power generator 70 with a proton exchange membrane (PEM) type fuel cell 152 which will be explained now. The apparatus 70 is shown in Fig. 8 and is similar to the one described in Fig. 7, with the exception that the exhaust gas from cracker 110 in line 240 is passed through a trace ammonia absorber 153 before being fed it to the anode side of the PEM fuel cell 152. This is required because the performance of the PEM fuel cell 152 is prone to be irreversibly degraded if even a few ppm of ammonia are present in the anode feed. The absorber 153 could be a cylindrical tube filled with absorbing material, Activated carbon treated with acid e.g. HzSO, acts as a good absorbing material for ammonia. Some metal ion exchanged Y-zeolite can also be used as the absorbing material. The absorber could be regenerated on site by heating it up under air flow or could be replaced together with the storage unit 120. Itis also possible to use at least two absorbers 153 in parallel to avoid stopping the operation of the power generator 70 when the absorber material is saturated, as shown Fig.9. The purpose of using more than one absorber 153 is to make the absorption process operating continuously: at least one absorber 153 will be in operation mode while the other one will be in the regeneration mode. If the absorber 153 contains a Cu-ion exchanged Y-zeolite as an absorbent, complete on-site regeneration is possible by heating the bed to 200°C while flowing air through the bed. This heat can be provided form one of the hot sources of energy in the system, e.g. combustion product gas. Yet another embodiment of the inventions is a continuous hydrogen generator, which will be will be explained now. This embodiment shown in Fig. 10 comprises two storage units 120 with embedded cracker units 1 (shown as UNIT 1 and UNIT 2), two heat exchangers 160, and a startup unit (SU) 170. During the start-up, ammonia can be pumped from the storage container 119, 120 of unit 4 to the thermal startup unit. The product gas from the start-up unit 170 (typically being 35% Hz and11% Nz and rest NHs) is mixed with air and passed through the heat exchanger 160 to the combustion chamber 2 of UNIT 1. The exhaust gas from the combustion chamber 2 exchanges heat with the inlet gas to the combustion chamber 2 in the heat exchanger 160. As soon as the combustion chamber 2 is10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 16 ready for ammonia combustion, the ammonia flow through the start-up unit is stopped and after mixing in the mixing chamber, referred to as Mixing Chamber 2 in Fig. 10, with air passed through one of the heat exchangers 160 (HE1). When the temperature of the cracker 110 is high enough for cracking, ammonia is fed to the cracker 110 by opening the proportional valve PV2, and the cracked product is taken out of the cracker 110. When storage unit 2 in UNIT 4 approaches depletion, a portion of the hydrogen produced can be diverted through proportional valve PV1 to Mixing Chamber 1 so as to mix with air. When cracker 110 in the UNIT 2 is ready for ammonia combustion, a portion of the ammonia~air mixture from Mixing Chamber 2 is passed to the combustion chamber 2 of UNIT 2 via one of the heat exchanger 160 (HE2). By the time the storage unit 2 in UNIT 1 is depleted, the second cracker 110 in UNIT 2 is ready for cracking ammonia. While storage unit 2 in UNIT 2 is running, storage unit 2 in UNIT 1 could be replaced with a filled one and the same cycle can be repeated when storage unit 2 in UNIT 2 is depleted, In Figure 10, each storage unit module 2 in UNIT 1 and UNIT 2 has a cracker 110 inserted during operation. However, as shown in Fig. 11, it can also be arranged that the jacket-cracker 110 is a stand-alone unit that is very well insulated, e.g. by vacuum-type insulation with radiation shield, and the heat of the exhaust gas provides the thermal energy to be transported to the ammonia storage unit or cartridge 400 that is in operation. This heat transfer can be accomplished by a heat exchanger zone that extends into the storage unit in a similar way as if the cracker 110 was inserted. It is also envisaged that the hot product gas from the jacket-cracker 110 can be provided to the storage unit(s) 400 externally, similarly to what has been mentioned about the integration of an external heat exchanger for the fuel cell coolant fluid. One such embodiment is also shown in Fig, 11, The combustion chamber exhaust gas after having exchanged heat with the combustion chamber feed, is passed on to provide heat of desorption to the ammonia storage cartridges 400. Depending on the process requirement, there could be one or more storage cartridges 400 absorbing heat from the combustion chamber exhaust. Because of the requirement that in the jacket-cracker 110 the combustion gas needs to transfer heat all along the length of the cracking chamber 1 at a very high temperature, for example not below 300 °C, but possibly10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 47 much higher, more heat is generated in the combustion chamber 2 than is consumed by the ammonia cracking reaction in the cracking chamber 1. This ensures that there is a great amount of recoverable heat available in the combustion exhaust gas. The combustion chamber exhaust gas, however, has to be above 50°C for effective heat exchange with the storage cartridge 400 for ammonia desorption. This can be ensured by methods including, but not limited to, varying the feed to the combustion chamber 2, changing the combustion to cracking ratio, and changing the size of the heat exchanger 160 used for transferring heat from the combustion exhaust gas to the combustion feed. In such an embodiment, only one cracker 110 has to be implemented in the system, even if several storage units 400 are a part of the complete hydrogen or power generating system 60, 70. It can also be envisaged that product gases from the jacket-cracker 110 exchange heat to a heat carrier fluid which carries the heat to the storage unit 400 for ammonia desorption. One such embodiment is shown in Fig. 12. Either one or both of the exhaust gases of cracker 110 transfer heat to a circulating fluid, e.g. silicone oil, which in turn transfers a part of the heat to one or more ammonia storage units 400. The heat carrying fluid can first exchange heat with the combustion chamber exhaust gas and then with the cracker chamber exhaust gas After exchanging heat with the combustion chamber exhaust a part or all of the flow can go on to exchange heat from the cracking chamber exhaust gas. The heat recovery from the jacket-cracker exhaust gas can also take place in the reverse order, i.e. first from the cracking chamber exhaust gas and then from the combustion chamber exhaust gas. The system can be integrated with fuel cell stacks as mentioned in the above paragraph for power generation operation. Ali documents cited in this specifications, such as patents, patent applications and journal articles, are herein incorporated by reference in their entirety. It is noted that the foregoing embodiments have been provided merely for the purpose of explanation and are in no way to be construed as limiting of the present invention. While the present invention has been described with reference to10 Wo 2011/107279 PCT/EP2011/001046 18 exemplary embodiments, it is understood that the words which have been used herein are words of description and illustration, rather than words of limitation. Changes may be made, within the purview of the appended claims, as presently stated and as amended, without departing from the scope and spirit of the present invention in its aspects. Although the present invention has been described herein with reference to particular means, materials and embodiments, the present invention is not intended to be limited to the particulars disclosed herein; rather, the present invention extends to all functionally equivalent structures, methods and uses, such as are within the scope of the appended claims.10 16 20 25 Wo 2011/107279 PCT/EP2011/001046 19 Claims, 1, An ammonia-based hydrogen generation reactor (110) comprising: - an ammonia cracking chamber (1) with an ammonia cracking catalyst, - an inner combustion chamber (2) with a combustion or oxidation catalyst being in thermal contact with the ammonia cracking chamber, - an ammonia gas preheating chamber (3), and - an outer jacket annulus (6) for recovery of heat from the combustion products exiting the combustion chamber (2), wherein the cracking chamber (1), the inner combustion chamber (2), the preheating chamber (3) and the heat recovery jacket annulus (6) are arranged concentrically in this order, the cracking chamber (1) forming the innermost chamber. 2. The hydrogen generation reactor (110) of claim 4 further comprising heat transfer fins (10) extending from the surface of the combustion chamber (2) into the cracking chamber (1), and flow distribution holes (5) enabling uniform feeding of ammonia to the cracking chamber (1) by flow through the flow distribution holes (5). 3. A system for generating hydrogen comprising at least one storage unit (119, 120, 400) containing a solid ammonia storage material (7) capable of releasing ammonia by desorption, preferably a metal ammine salt, which, when in operation, is combined with at least one hydrogen generation reactor (110) of claim 1, wherein, when in operation, the waste heat of the at least one hydrogen generation reactor (110) is transferred to at least one storage unit (119, 120, 400) being in operation. 4. The system of claim 3, wherein the at least one storage unit (119, 120) has a hollow concentric channel (8) extending partly or all the way through the unit in which, when in operation, one of the at least one said hydrogen generating reactor (110) is inserted10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 20 5. The system of claim 4, wherein the solid ammonia storage material (7) in the storage unit(s) (119, 120) is used as a part of a thermal insulation between the hydrogen generation reactor (110) operated at a temperature higher than 300°C and the surroundings. 6. The system of claim 4 or 5, wherein the storage unit(s) (120) has an annular chamber ($) at the outer side with an inlet and outlet for fluid functioning as a heat exchanger for providing heat to desorb ammonia. 7. The system of any of claims 4 to 6, wherein the storage unit(s) (119, 120) has a space 11 between the hydrogen generating reactor (110) and an inner wall of the storage unit (119, 120), when said hydrogen generating reactor (110) is inserted. 8. The system of claim 7 wherein the hydrogen generation reactor (110) is operated at a temperature higher than 300°C in which the space 11 can be varied or the space (11) is filled with a fluid which can be changed, so as to control the heat transfer between the hydrogen generating reactor (110) and the storage unit (119, 120), 9. The system of any of claims 4 to 8 further comprising a start-up unit (170) to assist the heating up of the combustion chamber (2) of the hydrogen generation reactor(110), and a heat exchanger (160) to recover heat of vaporization of steam formed in the combustion chamber (2) and to mix the ammonia from the storage unit (119,120) and air for entry into the combustion chamber (2). 10. The system of any of claims 4 to 9 comprising two modules, each comprising one of said a least one storage unit (119, 120) having a hollow concentric channel (8) extending partly or all the way through the unit in which, when in operation, one of said at least one hydrogen generating reactor (110) is inserted. 11. The system of claim 3, comprising at least two storage units (400) and one well isolated hydrogen generation reactor (110) as a stand-alone unit one well10 15 20 25 30 Wo 2011/107279 PCT/EP2011/001046 a isolated hydrogen generation reactor (110) as a stand-alone unit from which the heat generated in the combustion chamber (2) can be provided to the at least two storage units (400) externally or can be provided to a heat exchanger zone that extends into the storage units (400) via valves which direct the combustions products sequentially to one of the at least two storage units (400) which is in operation. 12. The system of claim 11, wherein the heat of the combustion products is delivered to the storage unit (400) via a heat exchanger (160) exchanging heat from the combustion products from the combustion chamber 2 and/or the crack products from cracking chamber 1 to a circulating liquid which delivers a part of the heat to at least one of the at least two storage units (400). 13. A power generation device (60, 70) comprising an alkaline fuel cell (151) or a PEM fuel cell (152) provided with an absorber (153) for absorbing traces of ammonia and the system for generating hydrogen of claim 4 from which hydrogen is fed to the alkaline fuel cell (151) or to the absorber (153), and after the absorption of traces of ammonia in the absorber (153) to the PEM fuel cell (152). 14. The power generation device of claim 13, further comprising a pump (180) which enhances the flow of ammonia from the storage unit (119, 120) to the hydrogen generating reactor (110), when a desorption pressure from the solid storage material (7) in the storage unit (2) is lower than a pressure level required to overcome the pressure drop during flow of ammonia through the power generation device (60, 70) 15. A power generating device (60, 70) comprising an alkaline fuel cell (151) ora PEM fuel cell (152) provided with at least one absorber (153) for absorbing traces of ammonia, the system for generating hydrogen of claim 11 or 12, from which hydrogen is fed to the alkaline fuel cell (151) or to the at least one absorber (153), and after the absorption of traces of ammonia in the at least one absorber (153) to the PEM fuel cell (152), and a pump (180) which enhances the flow of ammonia from the storage unit(s) (400) to the hydrogen generating reactor (110) when the10 Wo 2011/107279 PCT/EP2011/001046 22 desorption pressure from the solid storage material (7) in the storage unit (2) is lower than the pressure level required to overcome the pressure drop during flow ‘of ammonia through the power generation device (60, 70). 16. A method for operating a system for generating hydrogen comprising at least one storage unit 119, 120, 400 containing a solid ammonia storage material 7 capable of releasing ammonia by desorption, preferably a metal ammine salt, wherein waste heat from the hydrogen generation reactor (110) is recovered and used to fully or partially deliver the heat of desorption of ammonia from the ammonia storage material (7) to the storage unit (2). 17. The method of claim 16, further including introducing fuel cell coolant fluid of a fuel cell to an outer jacket of the storage unit (2) through a tube and returning the coolant fluid after exchanging heat with the ammonia storage material (7).Wo 2011/107279 PCT/EP2011/001046 w4 110 chamber Combustion Preheating Combustion (1) chamber (2) chamber (3) a exhaust <——— NH > H2 + NotNH3, +N + Air — ms > Ha + NotNHs SS Outer annulus (6) Combustion exhaust Fig. 1Wo 2011/107279 PCT/EP2011/001046 nt ‘Ammonia inlet flow distribution hole (5) Outer annulus NH, preheater Cracking chamber fin Combustion chamber Fig. 2Wo 2011/107279 3st PCT/EP2011/001046 119 —»| i i i i i i i i i i i i i i i i i i i i 120-—> i i i i i t i Fig. 4Wo 2011/107279 PCT/EP2011/001046 4nt Metal ammine/salt Space between the cracker and the storage unit wall Jacket- cracker Storage unit wall (110) Fig.SWo 2011/107279 PCT/EP2011/001046 s/t 50 120 180 H+ N, >, | Store 200 10 Tsscanaeoeesteammemsan |e cerns a ' Lchamber | + NH, i : 21 : i 250 combustion | | Start up unit P| chamber | | Heat 230 Hy#N,+NH, exchanger fg aa 220| | 5, \ Air ov Fig. 6Wo 2011/107279 6/11 300 PCT/EP2011/001046 Alkaline Fuel Cell a 151 120 NH, 210 Fuel Cell a Cracking chamber Combustion 750 i y| chamber NH, Heat exchanger le 297 \ 160 260 230 Fig. 7Wo 2011/107279 300 PCT/EP2011/001046 74 PEM Fuel Cell 210 ¥ ty Cracking chamber Heat exchanger ft} chamber 152 ee Air 70 . 153 290 3 LS 120 2 7 3 Radiato & | 201 [wet * Hy+N nq 200 en Start up unit H,+N, NH \ 260 170 Fig. 8Wo 2011/107279 PCT/EP2011/001046 art 300 PEM Fuel Cell 270 ‘Absorber Absorber Heat exchanger 120 & \ : L4 ni 4 {| Cracking + | chamber 210 i 250 } | Combustion [—t>|__chamber {_____y} t — Hy#N,+NH, 170 260 Fig. 9Fig. 10Wo 2011/107279 PCT/EP2011/001046 10/41 om Ny Storage units 400 (Cracking chamber sedoteactr MAA —— & Fig. 11Wo 2011/107279 PCT/EP2011/001046 111 Heehy (To etc) = te Serge eee es AW Fig. 12INTERNATIONAL SEARCH REPORT Teterational aplication No PCT/EP2011/001046 Nit HIMB/ Be BoIdi9/24 ADD. According to Intemational Patent Cassfeaton (PC) or tobothnatona elatttoaton and IPC HOIM BOlJ ‘nimum documentation aearsved lassfcaon ayaa flowed by daneicabon a7 Bam) Dosurrenaton searched Sher an ranrum docurentaion othe Hert Wal auahGasumnlsSre waded ithe hails Seana EPO-Internal Testor database consul during ie Wlamatonal search (name oT dal base ard, whee prasibal Seah TwTs wood) {DOCUMENTS CONSIDERED TO BE RELEVANT ‘aepo07" Chaton af dosumeat with ndaton, where appropiate, ofthe relevant pateagee x GB 1 336 375 A (VARTA AG) 7 November 1973 (1973-11-07) figure 1 page 1, lines 51-76 page 2, lines 30-33 page 2, paragraph 100-112 x GB 1 092 380 A (ALLIS CHALMERS 22 November 1967 (1967-11-22) figure 1 page 1, lines 34-53 page 2, line 90 - page 3, line page 4, lines 13-54 1,2 MFG CO) 1 90 X] Ferherdoourents ar inte inthe sontnuation of Box ©. XK] S00 patent amy annex soit Sperasn © quran eae anti a *P doeumantpublahed porto the intemationl ing date but ter then the prov date came “lator document published ater he inemational fling date ‘rprrty dat and nosn conic wy ie spplonsan ot Stedto understand ie prinapior ery wer he “7% eoument f parisarevace he inc ewenon, ‘nvowe on svete sop where soaumert tke lone "donut parolee theca imation train, sch comnaton emg cbs person sled 2° document member ofthe eame patent ay 7 June 2011 ‘Date of maling of he wieranal seek Topo 16/06/2011 European Patent Oe, PB. S818 Ptentinan2 NL“ 2200 HV Riewhe Tel ato) 1483000, Fax (281-70) 340-5016 Jacquinot, Patrick Fa POTTSAaIO exons hon) Roa DH page 1 of 2INTERNATIONAL SEARCH REPORT Teterational aplication No [68]; LIVESEY ALASTAIR KEITH [GB]; HODKINSON RONALD) 13 August 2009 (2009-08-13) page 7, line 29-- page 8, line 2; figures 1,3,4 page 26, line 3 - page 29, line 5 PCT/EP2011/001046 ‘iContinuaion) DOCUMENTS CONSIDERED TO BE RELEVANT ‘category | ciation of document wth ndeatin, where appropriate, othe relevantpasseges Relevant claim No. A Us 2007/207351 Al (CHRISTENSEN CLAUS H 3-17 [Dk] ET AL) 6 September 2007 (2007-09-06) figure 3 paragraphs [0053] - [0059], [0064] - [e069], [0088] - [0090} example 4 A DE 10 2006 061370 Al (ANMINEX AS [DK]) 3-17 26 June 2008 (2008-06-26) claim 21 Paragraphs [0017], [0023] A WO 2009/098452 A2 (DIVERSE ENERGY LTD 3-17 Fam POTTSH210 foninaan Sacer Seah TB page 2 of 2INTERNATIONAL SEARCH REPORT Teterational aplication No mation on patent family members PCT/EP2011/001046 Patent dooument Publeaton Patettamiy Prubleaion cited sareh report ste member) ‘ase GB 1336375 A 07-11-1973 DE 2022377 AL 25-11-1971 FR 2088438 AL 07-01-1972 6B 1092380 A 22-11-1967 BE 685876 A 23-02-1967 US 2007207351 Al 06-09-2007 AT 417374 T 15-12-2008 cn 1934741 A 21-03-2007 WO 2005091418 Az 29-09-2005, EP 1728290 A2 06-12-2006 Es 2319209 13 05-05-2009 JP 2007531209 T 01-11-2007 DE 102006061370 Al 26-06-2008 CN 101541401 A 23-09-2009 EP 2107933 Az 14-10-2009 EP 2316558 AL 04-05-2011 WO 2008077652 Az 03-07-2008 US 2010062296 Al 11-03-2010 WO 2009098452 AZ 13-08-2009 2276693 A2 26-01-2011