Patent Application
20250025848
The invention relates to a process and apparatus for developing a cracking reaction of hydrocarbon feeds so as to obtain a stream of gaseous hydrogen and solid carbon by means of a process which minimizes or totally eliminates CO2 emissions into the atmosphere; this is obtainable, according to the present invention, by a process in which the cracking reaction is developed inside a molten pool consisting of molten metals and/or molten salts in which the heat required for the cracking reaction is supplied by the electric current produced by applying an electric field by means of electrodes directly immersed in said molten pool.
It is known that the conversion of natural gas or other hydrocarbons into H2 can be carried out by different methods; for example, among those most used today, steam reforming (SR), autothermal reforming (ATR), partial oxidation with catalyst (CPO), or without catalyst (POx) can be mentioned.
In particular, partial oxidation in the absence of catalyst (POx) is preferably used for the gasification of heavy residues deriving from refinery activities, or even for the gasification of coke or other compounds originating from biomass.
In all the aforementioned technologies, the carbon atoms are converted into carbon dioxide (CO2) resulting in a significant CO2 emission associated with the production of said H2.
For example, natural gas (NG) Steam Reforming is commonly used for the production of about 94% v/v of the world's H2 production; this process releases about 10 kg of CO2 per kg of H2 produced.
Therefore, an apparatus for the conversion of natural gas (NG), or in any case of hydrocarbons, into H2, which avoids or in any case minimizes CO2 emissions, is highly desirable.
From this point of view, cracking natural gas inside a molten medium, for example in a molten metal and/or molten salt in the presence or absence of a catalyst, is an option and a very interesting alternative for producing H2 without CO2 emissions.
As known, the cracking reaction of methane (1) is sufficiently endothermic, as shown by the following reaction:
However, methane cracking is only one example of the simplest case of a wide range of saturated hydrocarbons which can be cleaved by breaking the C—H bond.
In fact, considering that the general formula for saturated acyclic hydrocarbons, i.e., alkanes, is CnH2n+2, the general cracking reaction can be written as follows:
Furthermore, the alkanes can be branched and/or saturated cyclic hydrocarbons, in addition to linear molecules, and are the basis of petroleum fuels.
Specific examples of alkane cracking are given in reactions 3 and 4 for propane and hexane, respectively:
In the configurations of liquid metal and/or molten salt reactors, known from the prior art and previously described and in which the methane cracking reaction occurs, external heating is generally used, for example by furnaces, through which the combustion heat is transferred to the molten medium.
Clearly, if fossil fuels are used to heat the reactor, the use thereof is such that they are CO2 emitters and this would nullify part of the CO2 emission savings which would instead be obtained by using the process according to reaction (1) to produce H2, where CO2 is not produced.
Similarly, burning H2 is a possible solution to the problem of CO2 emissions, but it obviously reduces the attractiveness of the final product of H2, which will inexorably be consumed to meet the thermal needs of the reactor.
Processes are known in which the heating is carried out by electrical elements surrounding the reactor, heating its walls; said hot walls thus transmit heat to the molten metal, for example tin, by convection and conduction.
In an industrial capability reactor this method creates a temperature gradient between the wall and the mass of the molten metal, causing uneven heating which is reflected in a decrease in the conversion yield of CH4 or, more generally, of hydrocarbons conversion.
Furthermore, in the CH4 cracking process inside the liquid metal, gas bubbles are formed in the reactor, linked to the distribution of the feed gas inside the molten metal bed; this implies, for technologies which use external heating, a reduction in the transfer of heat from the wall to the mass, due exactly to the generation of a higher temperature gradient, from which derives, in addition to the reduction of the efficiency of the electric heater, also a shortening of the life thereof.
Finally, still in industrial capability reactors, the combination of the operating temperature (900-1300° C.) and the molten medium, for example tin, does not allow the construction of walls made of metal, but rather of alloys with a high nickel content, such as Inconel, while the area of contact with the tin must be covered with a layer of ceramic bricks which create insulation but at the same time generate a resistance to heat transfer from the external heating.
For all the above reasons, heating is the main obstacle to the use of CH4 cracking technology in molten metal or salt reactors, in particular when CO2 emissions are to be minimized by using renewable energy for such a heating.
Even the solution of circulating a molten metal flow outside the reactor, such as tin, and heating it separately in an electric heat exchanger before recirculating it to the reactor, shows several problems mainly due to the fact that any metal used on the side cooling circuit is subject to a severe corrosion attack by the molten metal, which corrosion is accentuated by the operating temperatures of the reactor, which can typically be in the range between 90° and 1300° C.
Some application examples of cracking in the presence of a molten medium are shown below.
The paper “Catalytic molten metals for the direct conversion of methane to hydrogen and separable carbon” by D. Chester Upham et al, Science 358, 917-921 (2017), shows the performance of systems consisting of active metals (such as Ni, Pt, Pd) dissolved in non-active molten metals at low melting point (such as In, Ga, Sn, Pb) for the conversion of methane (CH4) to hydrogen (H2) and separable carbon; however, the paper does not specify the method used to heat and maintain the molten metal at the optimal temperature for the conversion of the load.
The paper “Fossil fuel decarbonation technology for mitigating global warning” by M. Steinberg, Int. J. Hydrogen Energy 1999, 21, 771-777, describes a molten-pool reactor which is heated through a tubular heat exchanger by combustion of methane-air or hydrogen-air; unlike the present invention in this solution, the metal is kept molten by means of either the combustion of methane, with subsequent production of CO2, or the consumption of hydrogen, thus leading to a consumption of the produced amount of this element.
In the study by Abanades et al. “Development of methane decarbonation based on liquid metal technology for CO2-free production of hydrogen”, Int. J. Hydrogen Energy 2016, 41, 8150-8167, a reactor is disclosed containing liquid metal, a subsequent separation step of the carbon from the liquid metal, a separation step of the carbon from the gas, a separation step of the hydrogen from the gas, and then recycling the raw material (methane) which has not reacted to the reactor; furthermore, the heating of the reactor is performed either by the combustion of the hydrogen produced, or by the combustion of the raw material, alternatively anticipating the use of solar energy.
In the paper “Hydrogen production using methane: techno-economics of decarbonizing fuels and chemicals” by Parkinson et al., Int. J. Hydrogen Energy 2018, 43, 2540-2555, the suggested scheme comprises a reactor containing a liquid molten metal on the top of which there is a molten salt layer and in which the reaction heat is supplied by an external furnace.
It is a fact, as can also be seen from the papers cited, that the cracking reaction of natural gas, being endothermic, requires the administration of heat.
However, if hydrogen is to be produced without CO2 emissions, it is apparent that such a heat must not be supplied by the combustion of fossil fuels.
Renewable or “green” electricity is a good solution to this problem, as described for example in the patents below.
Patent WO 2020/200522 A1 describes a geometry of endothermic reactors where the reaction zone consists of electrically conductive solid particles which are heated by means of the application of an electric field.
Unlike the present invention, however, a solid bed and not a molten metal is used as a heat conductor for developing the cracking reaction.
Patent U.S. Pat. No. 2,799,640, Jul. 16, 1957, describes a method and an apparatus for chemical reactions activated by electrocution; in this case, a fluidized bed reactor is disclosed in which said bed consists of conductive solid particles among which high melting temperature metals are expressly mentioned.
Patent U.S. Pat. No. 2,982,622, May 2, 1961, describes a method for converting a feed consisting of hydrocarbons (900-1700° C.) into hydrogen and pure carbon by means of electric current, in areas where the cost of electric energy is relatively low; also in this case a fluidized bed consisting of inert solid particles, or solid carbon-based particles, is included in the reaction zone.
Patent AT 175243 discloses an electric furnace having two vertically arranged electrodes adapted to transfer current to the bulk material present in the furnace compartment; the bulk material described can either participate in the reaction as a reagent, and thus be consumed by the same reaction, or act as a means for transmitting the generated heat; however, no mention is made of the use of molten metals and/or molten salts.
Patent CH 278580 discloses a blast furnace having two vertically arranged annular electrodes for transferring current to the bulk material present in said blast furnace; also in this case the bulk material described can either participate in the reaction, as a reagent, and thus be consumed by the same reaction, or act as a means for transmitting the generated heat.
The aim of the present invention is to overcome the limits of the prior art by providing an apparatus capable of converting natural gas, or in any case hydrocarbons, into hydrogen (H2), reducing or avoiding the conversion into CO2 and, therefore, the emissions of the latter into the atmosphere, in a medium consisting of molten metal and/or salt.
The suggested solution is to use a conversion reactor in which the heat required for the hydrocarbon conversion reaction into hydrogen and carbon is supplied by means of an electric current which propagates within a molten metal and/or salt appropriately controlled through the gas mass present in the bed, said gas mass consisting of the feed gas which is added to the recycle gas, with the addition, if any, of an inert material which lowers the conductivity of the molten pool.
A better understanding of the invention will be obtained from the following detailed description and with reference to the accompanying figures showing, by way of a non-limiting example, a preferred embodiment.
In the drawings:
The present invention relates to a process and apparatus for cracking natural gas, or other saturated hydrocarbon, in a molten medium such as metal and/or salt, so as to obtain a hydrogen-rich gas phase and a carbonaceous solid phase.
Such a solution allows reducing or completely avoiding CO2 emissions, normally related to the supply of the reaction heat through a heating furnace outside the conversion reactor, introducing a system directly into the reaction environment which exploits an electric current to generate the heat required for the cracking reaction through the Joule effect.
The solution disclosed is further capable of improving the heat transfer efficiency to the reactive species from a value of about 50%, considering the heating outside the reactor, to about 95%, while allowing the use of fossil fuels to be reduced or avoided and to allow the use of renewable energy sources to produce the required electricity consumption.
According to the invention, such an object is achieved by supplying the heat required for the cracking reaction by directly connecting the molten metal with an electrical circuit and then heating said molten metal pool, and/or molten salts, with the current passing therethrough.
This heating method is known as resistance heating, or ohmic heating, and includes the passage of an electric current through the medium and is obtainable by inserting electrodes directly into said molten medium; the natural resistance of the molten pool and the electrodes immersed therein, which we will indicate hereinafter for brevity “resistant system” to the passage 4 current generates heat, according to Joule's law, as universally known.
According to the invention, such a molten medium can be tin, lead, molten alloys such as Ni—Bi or molten salts and operates at a temperature below 1500° C., obtaining a hydrogen yield greater than 50%.
Since molten metals are relatively good conductors, having a low resistance to electric current, it is required to pass a large amount of current through the molten metal to transmit the necessary amount of heat for the cracking reaction to said molten metal; said power is calculated according to the following known formula:
P=I
2
*r=VI
According to a peculiar feature of the invention, the feed, natural gas or other hydrocarbon to which the recycling of the unconverted gas is added, is blown, in the gas phase, at the bottom of the reactor in the molten metal, so that said gaseous stream uniformly crosses the entire molten pool.
This peculiarity has an advantage: the presence of gas bubbles inside the liquid metal creates an empty volume which increases the resistivity of the molten pool, thus reducing the current to supply to obtain a heat input useful for developing the reaction, as shown in
Furthermore, the presence of gas bubbles affects the variation of the overall heat exchange coefficient, while allowing the removal of heat from the electrodes and favoring the heat exchange between the electrodes and the molten pool.
Basically, the conditions of the electric field are determined based on the average electric conductivity which exists in the resistant system (electrodes and molten pool) when it contains a certain amount of gas bubbles (empty volume): in fact, the presence of low conductivity material in the molten pool improves the control of the conductivity thereof and the removal of heat from the electrodes.
But there is further advantage: in fact, said electric field can also improve the kinetics of the cracking process due to the free radicals and ions contained within the gas bubbles, once the cracking temperatures are reached.
Furthermore, the heating is easily controllable according to the desired temperature of the medium inside the reactor, optimizing the current/voltage intensity conditions.
In a preferred, non-limiting embodiment, the voltage (V) to be applied to obtain the development of the cracking reaction is less than 100 V, more preferably is in the range of 5-75 V; furthermore the current intensity (I) applied is less than 500 A and the current density is in the range of 1-20 A/dm2.
Power can also be applied in direct current (DC) mode if the source is, for example, a photovoltaic system.
In particular, the application of a direct current allows having more effective control on the conversion of the power supply into hydrogen with the same electrical conductivity; moreover, advantageously, when the electricity is generated from a renewable source, such as photovoltaic or wind energy, the entire cracking process is completely free of CO2 emissions.
According to the invention, the heating method now described can be applied to either a molten metal, or an alloy as previously indicated, or to a molten metal in which a homogeneous catalyst is dissolved or alloyed, by way of non-limiting example, a small percentage of Ni.
Furthermore, different electrode arrangements and configurations are possible, as shown in
According to the invention, the electrodes can be made of materials such as graphite, carbides (e.g., Sic, ZrC), nitrides (e.g., AlN), borides (e.g., ZrB2, ZnB2) as well as yttrium-stabilized zirconia (YsZr).
Up to an operating temperature of 1100-1200° C., the material SiC is an excellent substitute for graphite by virtue of the better mechanical properties and high availability.
As already described, the electrically heated reactor can contain an active catalytic metal melted or alloyed in the metal pool, so as to form a molten metal alloy, where the active metal is Ni or an Ni alloy such as Nickel-Gallium, or Gallium and alloys thereof, or copper (Cu) and the alloy thereof or any combination of the aforementioned metals.
Advantageously, the presence of a catalyst increases the single-passage conversion of the feed and lowers the operating temperature, approaching the thermodynamic limit of the methane cracking at that temperature.
The gas stream produced by the cracking reaction is rich in H2 and can be directed to purification treatments (such as PSA) to obtain pure hydrogen while the unconverted gas is recycled and mixed with the feed; in this sense a general diagram is shown in
Advantageously, the solid carbon obtained from the cracking reaction is insoluble with the molten metal and therefore will separate therefrom, accumulating on the upper surface from which it can be separated; this implies that the carbon advantageously does not saturate the molten metal and that therefore, in the presence of a catalyst dissolved in the molten pool, it is not able to poison or deactivate the catalyst.
According to the invention, various configurations of the electrodes immersed in the molten pool are possible.
For example,
A second arrangement is shown in
A third arrangement is shown in
A fourth arrangement is shown in
In the preferred embodiment shown in
In the embodiment described in
The conversion process described above is implementable both at moderate pressures and under medium/high pressure conditions: this allows the reactor to be appropriately sized according to the desired operating pressure and the subsequent steps downstream thereof.
In fact, if the reactor operates at a sufficiently high pressure, it is possible to optimize the entire gas circuit downstream of the reactor, since no intermediate compressor would be necessary to bring the converted gas to the pressure conditions suitable for the subsequent purification step in the PSA unit.
In the preferred embodiment described, the anode cooling can be achieved by preheating the natural gas feed flowing through the electrode itself, said electrode having the shape of a tube or by an external cooling medium such as water or air.
Furthermore, the electrode cage is supported by a structure thereof which allows the regular maintenance thereof.
According to the invention, the estimated energy consumption is in the range of 5-20 KWh per kg of hydrogen produced, better still in the range of 5-10 KWh per kg.
In the described preferred embodiment, the electrical resistance of the molten metal is controlled by the size and number of the natural gas bubbles and this is achieved by using a porous diffuser or spreaders.
In a preferred, non-limiting embodiment, the size of the bubbles will be less than 1 mm.
By way of example, it has been estimated that at 800° C. a conversion per step of 90% can be obtained in the presence of a suitable catalyst.
The method according to the invention is also usable with alternative feeds other than natural gas; in fact, the raw material to be treated could be any other fossil hydrocarbon either as gas or liquid or even organic waste streams.
Furthermore, it is possible to improve the reaction kinetics by immersing the filler material inside the molten medium to facilitate the heat transfer between the medium and the bubbles and by slowing the rate of rise of the bubble and increasing the residence time; said filler material is mainly ceramic which can have different shapes, for example rings, saddles, etc.
Although various embodiments have been provided in the present disclosure as illustrative and non-restrictive examples, it should be clear that the systems and methods disclosed can be incorporated into many other specific embodiments without departing from the spirit and scope of the present description.
Many other modifications, equivalents and alternatives, will become apparent to those skilled in the art once the above description has been fully appreciated. It is understood that the following statements shall be construed to encompass all such modifications, equivalents and alternatives where applicable.
From the above description, many advantages are apparent.
A first advantage of the invention consists in reducing, if not eliminating, CO2 emissions in the hydrogen and hydrocarbon cracking process.
A second advantage of the heating method according to the invention is related to the scalability up to large diameter industrial capacity reactors, which usually consist of metal tanks internally coated with ceramic bricks; this allows solving one of the major problems encountered by most of the suggested prior art indicated above.
Furthermore, the method according to the invention efficiently uses electrical energy, is clean and produces uniform heating of the fluid without temperature gradients with respect to heating from the outside and through the walls of the molten metal reactor.
A further advantage of the invention consists in the better management of the chemical reaction, easily controllable, in terms of conversion, simply by controlling the value of the applied voltage.
Finally, a further advantage consists in that the solid carbon produced by the reaction naturally separates from the molten pool, not saturating the metal and, in case of the presence of a catalyst dissolved in the molten pool, does not deactivate or poison said catalyst; this translates into a better management of the catalyst itself which does not need constant regeneration.
The example shown in
Taking a medium temperature of 800° C. as a reference, the electrical resistivity goes from 0.67, 0.94 and 1.55 ohm·m for a degree of vacuum of the molten tin pool of 5%, 25% and 50% respectively.
Based on these considerations, it was estimated that for the production of 100 Nm3/h of H2, a power of about 50 KW is required, obtained for example by a voltage of about 100 V and a current of 500 A.
A greater capacity can be achieved by multiplying the number of modules or changing the electrode arrangement.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102021000029045 | Nov 2021 | IT | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2022/060932 | 11/14/2022 | WO |
