METHOD AND SYSTEM FOR PRODUCING A SOURCE OF THERMODYNAMIC ENERGY BY CO2 CONVERSION FROM CARBON-CONTAINING RAW MATERIALS

Description

[0001] The invention refers to a process to produce convertible thermodynamic power (into electricity, etc.) from raw material containing carbon. It also refers to a system to perform such a process.

[0002] The field of the invention is the production of electricity from raw material containing carbon and, more particularly, from coal and/or dry biomass.

[0003] The production of electricity by double generation (cogeneration) from thermal power as obtained by burning fuel raw material containing carbon is a process which is very well-known by the experts in the art.

[0004] This process consists, in its most generic version, in using the heat of biomass combustion to heat a fluid which is then used in a system for cogeneration of electricity, such as a turbo alternator.

[0005] However, the processes and systems to generate electricity from carbon raw materials inconveniently need to perform the combustion of the material, so to transfer as much power potential produced by said combustion as possible. In all combustions, there is a yielding corollary: the yielding of the combustion as related to the quality and grade of humidity of said carbon material and the global thermal yielding relative to the thermal generator, its configuration, its combustion yielding (and consequently the incidence of incrustation (deposit of non-burnt material) caused by more or less complete combustion, reducing progressively and rather quickly the yielding of the thermal exchange of the thermal generator).

[0006] In existing systems, the most widely used method for combustion is performed under oxidizing atmosphere, i. e. wherein the fuel of said raw material containing carbon is surrounding air. Global yielding of said thermal generators is approximately 85% PCI (lower heating power) of the carbon-containing material as used, wherein maintenance requirements are relative to the quality and humidity rate of said carbon raw material.

[0007] The systems of this kind generate a combustion gas (smokes) more or less loaded with dusts, COV (volatile organic compounds), NOx, complex pollutant molecules (methane, carbon monoxide, dioxins, PCB, etc.) and the CO₂ relative to the combustion of carbon as contained in said raw material containing carbon. At least 15% of PCI of said carbon raw material are dispersed through smokes and incombustible products. PCI of said carbon raw material varies, when referring to vegetal and/or animal biomass, between 2 and 5.2 kWh/kg as a function of its relative humidity (i. e. transferred global thermal yielding between 1.7 and 4.4 kWh/kg); or when referring to fossil carbon: between 6 and 8 kWh/kg as a function of its carbon concentration (i. e. transferred global thermal yielding between 5.1 and 6.8 kWh/kg). CO₂ rate as contained in smokes of the current systems is between 10 and 18% per Nm³ of smokes and its concentration for eventual stocking and/or sequestration needs complex and expensive processes.

[0008] In the past few years, new systems and processes were put into practice to optimize the yielding of combustion and CO₂ concentrations in smokes: it mainly refers to oxidizing agents enriched with oxygen, up to pure oxycombustion systems. These systems and processes considerably increase global thermal yielding and smokes are less harmful to the environment, since they are essentially composed of CO₂, which can be easily captured. However, these systems and processes depend on a continued supply of oxygen, and therefore its production is expensive and not free from impact to the environment.

[0009] US 4,272,555 describes another system and process for converting carbon-containing materials to carbon oxides wherein the carbon-containing materials are gasified using a metal oxide as the oxygen and heat source for the gasification with carbon monoxide.

[0010] An object of the present invention is to avoid the inconveniences as mentioned above.

[0011] Another object of the present invention is to offer a process and a system for the production of electricity from biomass containing carbon. Whether the mentioned carbon biomass is fossil or not (carbon and/or plant and/or animal biomass and/or residues/garbage) containing enough carbon for its exploration, it can contain molecular hydrogen. Under this condition, reactions as disclosed below are identical, just varying the final results as related to the molar mass difference between carbon and hydrogen (1 mol of C = 12 g, 1 mol of H₂ = 2.016 g). The oxidation of that hydrogen in the reaction chain produces water steam which will be condensed and recovered in said reaction chain as disclosed below, as well as the resulting intrinsic heat. Whether the carbon-containing raw material contains hydrogen or not does not have essential influence over the object of the invention: the production of electricity, or over its yielding. The present disclosure of the invention therefore considers a material essentially composed by carbon (fossil coal, vegetal coal, coal from the pyrolysis of organic biomass, etc.), not however excluding plant and/or animal biomass and/or carbon residues, which should be conditioned and dry. The preparation of carbon materials as mentioned consists in crushing/milling (which optimizes the yielding of pyrolytic reactions) and drying, if necessary.

[0012] The invention allows to reach the above mentioned objects by means of a process to produce electricity from carbon raw material (MPC) and, more particularly, from carbon biomass (BC), which process comprises at least an iteration of the following steps, constituting a treatment cycle:

• gasification in a first so-called gasification reactor of carbon-containing raw material with a gaseous flow of gasification containing CO₂ at high temperature, said gasification supplying a first gaseous flow essentially containing molecules of carbon monoxide (CO);
• oxidation in a second so-called "oxidation" reactor by said oxygen holders in oxidized state, said molecules of carbon monoxide (CO) being present in said first gaseous flow, said oxidation supplying a second gaseous flow at high temperature containing CO₂ and oxygen holders in reduced state (Me);
• activation, in a third so-called "activation" reactor, of said oxygen holders in reduced state with a so-called gaseous flow of "activation" containing elements of oxygen, wherein said oxidation supplies oxygen holders in oxide state and an oxygen-poor gaseous flow of activation at high temperature;
• transference of a part of the thermal power as generated during the gasification to the oxygen-poor gaseous flow of activation;
• conversion into electricity of at least a part of the thermal power of said oxygen-poor gaseous flow of activation at high temperature, e. g. by a steam generator/thermal exchanger system and a turbo alternator, to convert steam into electricity.

[0013] The process of the invention allows to give value to the energy from the raw material containing carbon with higher yielding than current processes and systems.

[0014] Oxygen holders may contain NiO, Fe₂O₃, MgO, CaO, etc.

[0015] The process of the invention allows to generate electricity from raw material containing carbon, not performing combustion of the biomass. In fact, the energy as contained in the biomass is recovered thanks to biomass gasification, a gaseous CO₂ flow (thermochemical reaction converting the CO₂ molecule over an element of carbon into two molecules of carbon monoxide CO).

[0016] Therefore, the gaseous flow of activation is pre-heated thanks to the thermal power by the process of the invention from MPC, i. e. with no supply of external energy.

[0017] Advantageously, the process of giving value to the thermal power of the oxygen-poor gaseous flow of activation under high temperature may additionally comprise a step of transference of at least one part of the thermal power from said oxygen-poor gaseous flow of activation to a so-called electricity generating fluid, supplied to a converter device for the production of electricity.

[0018] On the other hand, the process of the invention may comprise the recovery of the residual thermal power from said oxygen-poor gaseous flow of activation, wherein at least a part of said residual thermal power is sent to the gaseous flow of gasification as used in the following treatment cycle.

[0019] Therefore, the process of the invention allows to grant value to the residual energy to pre-heat the gaseous flow of gasification, thus avoiding to use external power supply.

[0020] The process of the invention may advantageously comprise a step of increasing the temperature of the raw material containing carbon before gasification by means of the transference of at least a part of the thermal power of the second gaseous flow under high temperature to said raw material.

[0021] The thermal power of that second gaseous flow is therefore equally valued in the process of the invention.

[0022] The process of the invention may additionally comprise recycling in closed circuit (loop) of at least a part of the CO₂ in the second gaseous flow to constitute said gaseous flow of gasification.

[0023] The process of the invention allows to recycle a part of that CO₂ flow to a new treatment cycle. Therefore, the impact of the process of the invention over the environment is limited.

[0024] Advantageously, the procedure of the invention may comprise, before the step of activation of oxygen holders, pre-heating of the gaseous flow of activation with the residual energy of the electricity generating fluid.

[0025] According to a specific version of the process of the invention, it can advantageously comprise the supply of a part of the second gaseous flow to a bioreactor containing microalgae. After refrigeration of the mentioned part of said second gaseous flow, said microalgae photosynthesize the CO₂ as present in the mentioned part of said second gaseous flow, supplying said bioreactor with, on one side, a gaseous flow of oxygen, and, on the other side, biomass containing carbon.

[0026] In this version, the process of the invention does not bring in any impact over the environment. On the other hand, in this specific version, the process of the invention produces at least a part of the raw material containing carbon, gasified in the system.

[0027] Still in this version of the process of the invention, a gaseous flow of oxygen is generated by microalgae. That gaseous flow of oxygen may receive value in the process of the invention, e. g. to generate electricity or thermal power for any of the steps of the process of the invention.

[0028] As an example, the process of the invention may comprise the recovery of at least a part of the flow of oxygen as generated by microalgae and an injection of at least a part of said flow of oxygen in the gasification reactor to complete the gasification of raw material containing carbon.

[0029] On the other hand, the process of the invention may comprise the recovery and a treatment of the biomass containing carbon as supplied by the bioreactor, due to the gasification of said biomass in the gasification reactor.

[0030] Another object of the invention proposes a system to produce electricity from raw material containing carbon, comprising:

• a gasification reactor of carbon-containing raw material with a gaseous flow of gasification containing CO₂ at high temperature, said reactor supplying a first gaseous flow containing molecules of carbon monoxide (CO);
• an oxidation reactor by oxygen holders in oxide state, being said molecules of carbon monoxide (CO) present in the first gaseous flow, wherein the reactor supplies a second gaseous flow under high temperature containing CO₂ and oxygen holders in reduced state;
• an activation reactor of said holders of oxygen in reduced state with a gaseous flow comprising elements of oxygen, said reactor supplying holders of oxygen in oxidized state and an excess of thermal power;
• means for transferring a part of the thermal power as generated during gasification to the gaseous oxygen-poor flow of activation;
• an electricity generation device from at least one part of said thermal exceeds from said activation.

[0031] The system of the invention may advantageously comprise mechanical means of transportation of the oxygen holders from the oxidation reactor to the activation reactor and/or from the activation reactor to the oxidation reactor.

[0032] On the other hand, the system of the invention may comprise a loop recycling circuit of a part of the CO₂ as present in the second gaseous flow as used as a gaseous flow of gasification.

[0033] The electricity generation device may comprise a turbo alternator or any equivalent device.

[0034] Advantageously, the system of the invention may comprise a bioreactor containing microalgae to which a part of the CO₂ as present in the second gaseous flow, wherein said microalgae photosynthesize said CO₂ and said reactor supplies, on one hand, a gaseous flow of oxygen and, on the other hand, biomass containing carbon.

[0035] Other advantages and characteristics will appear from the analysis of the detailed description of a non-limitative way of embodiment and the attached figures:

• Figure 1 is a schematic representation of a first way of embodiment of a system of the invention; and
• Figure 2 is a schematic representation of a second way of embodiment of a system of the invention.

[0036] In the figures, the elements appearing in all of them receive the same reference.

[0037] Figure 1 is a schematic representation of a first way of embodiment of the system of the invention.

[0038] The system 100 comprises a gasification reactor 102, an oxidation reactor 104 and an activation reactor for oxygen holders 106.

[0039] The gasification reactor is composed of two communicating and concomitant parts:

• a feeding chamber (sas) 108 for dried carbon-containing materials, comprising a mechanized feeding valve (not shown) under control of CO₂ to avoid any entrance of air and guarantee the hermeticity of the system; and
• a CO₂ converter 110 over the raw material containing carbon as properly stated.

[0040] In the feeding chamber 108, dry materials containing carbon indicated as C in the figures are pre-heated by contact, convection and osmosis by a hot gaseous flow of CO₂. We will see further below that this gaseous flow of CO₂ is produced and pre-heated by the system 100. This gaseous flow of CO₂ crosses dry materials containing carbon C, transferring to them their thermal capacity. In the course of its introduction in this sector, through a mechanized feeding valve, which air hermeticity is assured by the CO₂ as injected under pressure, the materials containing carbon absorb the sensible heat of CO₂. Said raw materials containing carbon are introduced by given sequences.

[0041] Dry raw materials containing carbon C subsequently flow by gravity in the converter 110 by means of tubular grids (not shown) reducing their speed.

[0042] A gaseous flow of gasification FGG essentially composed by reactive CO₂ under high temperature is introduced in the gasification reactor 102. The reactive CO₂ is at a temperature of 900/1000 °C or higher. It is injected into the gasification reactor in counter current from the flow of materials containing carbon C, after circulation in the tubes of deceleration grids. Said tubular grids perform the role of a heat exchanger with materials containing carbon, adding large thermal complementation, useful to conversion, with a role of flow retardant for the raw materials in the gasification reactor.

[0043] CO₂ as introduced finds the dry material containing carbon C which, in this step, reached a temperature near 900/1000 °C. The reaction of the meeting is the conversion of CO₂ into CO, and therefore in power. This energy fully transfers the power potential of materials containing carbon C to the following reactive sectors in the system 100.

[0044] The conversion reactor (I) from CO₂ to CO is endothermal, according to the reactions:

        CO₂ - ½ O₂ = CO + O + 283 kJ/mol

        C + ½ O₂ (from CO₂) = CO - 111 kJ/mol

[0045] Consider a thermal deficit of 172 kJ/mol of CO₂ converted in CO by C. Each of the two molecules of CO as obtained has a heating power of 283 kJ/mol, i. e. a total 566 kJ, while the heating power of C (material containing carbon with primary reaction energy) is 394 kJ/mol. Under these conditions, the main object is, therefore, to supply 172 kJ from the conversion reaction by means not imputable to this power potential or by external thermal means by introducing another power to compromise such yielding. We will see in the disclosure below how the system of the invention reaches this object.

[0046] In the outlet of the gasification reactor 102, a first gaseous flow PFG essentially comprising CO at a temperature of more than 900 °C. This first gaseous flow PFG is therefore eminently full of power and reactive. It allows the transference of the potential energy of raw materials containing carbon to the oxidation reactor 104. Therefore, it is introduced in the oxidation reactor 104, wherein it will be oxidized in contact with oxygen-holding materials MeO in oxidized or active state.

[0047] The active oxygen holders MeO are introduced in the oxidation reactor 104 at the level of an upper part of that reactor 104 and flow through tubular grids (not shown) decelerating this flow.

[0048] The first gaseous flow coming from the gasification reactor 102 essentially comprising CO is at a temperature of more than 900 °C. It is introduced in the oxidation reactor 104 at the level of a lower part of that reactor 104 in counter current to the flow of oxygen holders MeO. The meeting between oxygen holders in oxide state MeO (or active) and the first gaseous flow causes:

• the oxidation of molecules of carbon monoxide CO into carbon dioxide CO₂; this reaction is exothermal and releases 283 kJ/mol; and
• the reduction of active oxygen holders MeO; this reaction is endothermal and absorbs 244.3 kJ/mol.

[0049] Therefore, the global reaction (II) is exothermal:

        2MeO - 2 ½ O₂ + 2 CO + 2 ½ O₂ = 2CO₂ + 2 Me

        +488.60 kJ - 566 kJ = - 77.4 kJ

[0050] The oxidation reactor 104 is therefore exothermal for 77.4 kJ by molar equivalent of CO₂, which will be deducted from the 172 kJ to be supplied to the reaction occurring inside the gasification reactor 102 as per reaction II as disclosed above.

[0051] Said oxidation reactor supplies a second gaseous flow DFG essentially comprising CO₂ at high temperature and oxygen holders Me in reduced state (deactivated).

[0052] The oxidation reactor 104 is kept at a correct temperature level (1000 °C or lower) thanks to the second gaseous flow DFG1 (part of the second gaseous flow DFG as recycled, after said second flow DFG changed its thermal capacity along the various thermal exchanges refrigerating it at the outlet of said oxidation reactor 104), regulating the temperature of said oxidation reactor 104, picking up the thermal excess in benefit of its useful thermal capacity to new iteration.

[0053] Said second gaseous flow DFG exiting from the oxidation reactor 104 goes through the feeding chamber 108 of dry materials containing carbon. Therefore, this second gaseous flow DFG is used to pre-heat the dry raw material containing carbon C, exchanging its sensitive heat (by contact, convection or osmosis) with said dry raw material C.

[0054] At the outlet of the feeding chamber 108, the second gaseous flow DFG is refrigerated at the admission temperature of the dry raw material containing carbon C at which its essential thermal capacity has been transferred. It is extracted from that chamber 108 by mechanical means (extractors/fans, not shown) keeping the whole system under depression.

[0055] Oxygen holders Me in reduced state are introduced into the activation reactor 106. The transference of oxygen holders from the oxidation reactor 104 to the activation reactor 106 is performed by mechanical means or by gravity, as per reactor configuration.

[0056] Deactivated oxygen holders Me are still at high temperature of about 800 °C and are eminently reactive. They flow to the activation reactor 106 by gravity by means of the tubular grid net (not shown) decelerating such flow. Tubular nets perform the role of a thermal exchanger, wherein the gaseous flow DFG1 circulates (a part of the second gaseous flow DFG as recycled), wherein it acquires the thermal capacity of gaseous flow of gasification FGG.

[0057] In the reactor 106, Me are reactivated by the oxygen of a gaseous flow of activation FA, which, in the present example, is from atmospheric air surrounding the counter current.

[0058] The oxidation of oxygen holders Me in contact with air is exothermal, the power supplied is 244.30 kJ/mol of Me, i. e. 488.60 kJ for both moles of Ni according to the reference option of oxygen holders in the disclosure of chain reaction.

[0059] This reactor supplies at the outlet a very hot oxygen-poor gaseous flow of activation FAA at temperatures of 1100 °C or lower and activated oxygen holders MeO at the same temperature.

[0060] The reacted oxygen holders in MeO are transferred to the oxidation reactor 104 by mechanical means or by gravity, as per reactor configuration.

[0061] The very hot oxygen-poor gaseous flow of activation FAA as obtained at the outlet of the activation reactor 106 is directed through an exchanger 112 through a gasification reactor 102 to a tubular net performing the role of exchanger and deaccelleration grids in said gasification reactor 102. This traject allows to keep the high temperature useful to the conversion reaction of CO₂ over C, not overloading the thermal capacity of the over-heated oxygen-poor gaseous flow FAA.

[0062] In the outlet of the gasification reactor 102, the over-heated oxygen-poor gaseous flow FAA is transferred in the exchanger 112, wherein it exchanges the essential part of its heat with an electricity generation fluid FGE.

[0063] Said electricity generation fluid is then supplied to a turboalternator 114 wherein the thermal power is transformed in electricity.

[0064] In the outlet of turboalternator 114, the electricity generating fluid FGE contains residual thermal power. In the outlet of the turboalternator 114, that fluid FGE is injected in another thermal exchanger 116 wherein the residual energy of the electricity generating fluid FGE is transferred to the gaseous flow of activation FA which will be used in a subsequent cycle of treatment to activate oxygen holders in the activation reactor 106. Therefore, the gaseous flow of activation FA as used in the subsequent cycle of treatment is pre-heated thanks to the thermal power as supplied directly by the system of the invention, not requiring an external power supply.

[0065] At the outlet of that second exchanger, the electricity generating fluid FGE is again injected in the first thermal exchanger 112 to start a new cycle.

[0066] Therefore, the electricity generating fluid FGE circulates in a closed circuit 118 interconnecting the first thermal exchanger 112, the turboalternator 114 and the second thermal exchanger 116.

[0067] A part DFG1 of the second cooled gaseous flow DFG extracted from the feeding chamber 108 of the gasification reactor is recycled and used as a gaseous flow of gasification for the following cycle. The other part DFG2 of the second gaseous flow is stocked or rejected in the atmosphere.

[0068] However, this flow DFG1 is cold and should be heated for use as a gaseous flow of gasification.

[0069] The oxygen-poor gaseous flow FAA exiting from the first thermal exchanger 112 after having transferred most of its thermal power with the electricity generating fluid FGE contains residual energy which is transferred to the gaseous flow DFG1 in a thermal exchanger 120.

[0070] This flow DFG1 subsequently travels in the tubular net (performing the role of tubular gids for deceleration of the flow of MeO and thermal exchanger) located in the oxidation reactor 104 to obtain a part of its thermal capacity and, at the same time, regulate the temperature of the oxidation reactor 104 at values of less than 1000 °C. Thanks to this transference of a part of the thermal power from the oxidation reactor 104, the second gaseous flow DFG transfers a part of its thermal capacity before its introduction in the feeding chamber 108 of the gasification reactor 102. Therefore, at the outlet of said oxidation reactor 104, a gaseous gasification flow FGG composed by the recycled part DFG1 of the second gaseous flow DFG, is obtained. The gaseous flow of gasification FGG as obtained at the outlet of the oxidation reactor 104 is then injected in the net of tubular grids (which perform the role of a thermal exchanger) of the activation reactor 106. It then acquires the whole working capacity for CO₂ conversion over the materials containing carbon, always keeping the temperature of the activation reactor below 1000 °C, absorbing the released excess of energy. At the outlet of the activation reactor 106, the gaseous flow of gasification FGG as obtained is injected in the converter 110 to perform the following cycle.

[0071] The second gaseous flow DFG essentially comprising CO₂ as generated by the oxidation reaction in the oxidation reactor 104 is composed by 2 moles which thermal capacity is 101.331 kJ, to which 77.40 kJ from the exothermal power of the reaction should be added, i. e.: 178.731 kJ to which we should exclude Cp (thermal capacity of coal at 1000 °C) of the coal at 1000 °C and Cp of the mole of CO₂ from recycled gasification and the conversion power, i. e.:

• thermal capacity of the carbon at 1000 °C - 14 kJ/mole (1 mole of C per 1 mole of CO₂); and
• enthalpy of the mole of CO₂ from recycled gasification = 50.67 kJ/mole Conversion energy = 172 kJ/mole of CO₂, i. e. a total:
  14 + 50.67 + 172 kJ - 236.67 kJ per mole of converted CO₂ by one mole of carbon (energy required to gasification).

[0072] In this step of recovery of the process energies, the thermal deficit is reduced to: 178.731 kJ - 236.67 = 57.939 kJ per mole of converted CO₂ by 1 mole of carbon. That thermal deficit of 57.939 kJ per mole of CO₂ is taken off the thermal power as supplied to the activation reactor 106 before the production process of thermodynamic energy and its coversion to electricity.

[0073] The thermal power of 236.67 per mole of converted CO₂, as consumed by the set of reactions, should be supplied at the start of the system. Then, the system is thermally autonomous, with the exception of the carbon supply.

[0074] In fact, as we have just disclosed, the system of the invention enables to produce/recover/recycle the required energies to increase the temperature of the raw material containing carbon and the different gaseous flows, and to perform the various reacions, reducing the initial thermal demand from 236.67 kJ to 57.939 kJ per mole of converted CO₂ (per one mole of carbon as used to generate electricity) along the following cycles.

[0075] In this stage of the process of the invention, 100% of the energy of a mole of carbon (MPC - raw material containing carbon) are transferred to the reaction chain to produce electricity (or thermodynamic energy/water steam) and the CO₂ produced by its full oxidation is pure and capturable with no other form of process and the conversion CO₂ is recycled.

[0076] The second gaseous flow DFG essentially comprising CO₂ is therefore almost pure (it may contain dust particles which will be retained by a classical filter). It is separated in two volumes by a registration set at the outlet of the feeding chamber 108 of the oxidation reactor 102. At least 50% are recycled to the system to constitute the gaseous flow of gasification for the next cycle of treatment.

[0077] The remaining volume DFG2 is collected "without any process" to be stocked or recycled in various applications. We should highlight that, for each cycle, this volume corresponds to the carbons as contained in the chemical formulation of the carbon material as introduced into the gasification reactor. The chain of reactions, conversions and energy transferences over these carbons only produces pure CO₂, and no other process and/or system is useful. This step really eliminates fully all current procedures aiming to the collection of CO₂, which will be very expensive.

[0078] In this step of the process of the invention, the solution on the negative environmental impact (of traditional facilities for the production of electricity from carbon-containing materials) is provided; in this step of the process of the invention, the thermal balance is unbalanced, with a deficit of 57.939 kJ per mole of converted CO₂ per one mole of carbon; in this step of the process of the invention, the chain of reactions has the oxidation energy of two moles of Me as generated in the activation reactor 106 to be transferred to the fluid FGE for conversion into electricity.

[0079] In conclusion, the thermal balance is as follows:

• the oxidation of the two moles of Me = 2 moles of MeO = 488.60 kJ less
• the thermal deficit in the oxidation reactor = 57.939 kJ per mole of converted CO₂ per one mole of carbon, i. e. a total of:
• 488.60 kJ - 57.939 = 430.661 kJ per one mole of carbon.

[0080] The compensation of said 57.939 kJ of the thermal deficit from process reactions of the invention is assured by:

• thermal transference of said 57.939 kJ of the thermal deficit of the overheated flow of air FAA to the gasification reaction by a thermal exchanger located in the gasification reactor 102; and/or
• a complementary recycling of CO₂ (1.15 mole of useful CO₂ to the supply of 57.939 kJ), which function will be of heat holder for said energy which is taken from the energy as supplied to the activation reactor 106.

[0081] This allows the following relationship: in a current system, the combustion of carbon (carbon-containing raw materials) degrades the power potential (especially for the thermal losses in smokes), wherein said lowering is defined by combustion yield, being the energy residue lowered by the losses related to the exchanges in the generator. The set of these lowerings gives us a total yield over PCS (if there is energy recovery from the condensation of water steam as contained in smokes) or over PCI (the most common data). For an efficient thermal generator, this global yielding is near 85% over PCI.

[0082] The maximum yield of conversion in electricity of a current facility is of 35% of PCI, taking into account the whole sum of degradations, from the combustion to the turboalternator, passing through the various exchangers.

[0083] The system of the invention also exchanges the heat of the reactions to water steam (electricity generation fluid FGE), which is introduced in the alternator of the turbin for conversion into electricity. If we take the evaporator as a point of reference, as included in both processes, the conventional combustion system and the system of the invention, this point defines the real yield of the conversion into electricity.

[0084] For both processes, the same thermal power for the introduced carbons (MPCS), i. e. a PCI 394 kJ/mol of C, is reserved.

[0085] In the combustion processes, the global yield in the generator is 85%, i. e. a thermal residue of 335 kJ/mol of C available in the evaporator. In these systems, the yield of conversion in electricity is 35% PCI, i. e.: 394 x 0.35 = 138 kJ elect/mole of C; if we make the relationship on the evaporator, the real yield of the conversion in electricity of the available power for this process is therefore: 138 x 100/335 = 41%.

[0086] The process of the invention makes thermochemical reactions which do not degrade the available power. In the same point of reference, we will then have 430.661 kJ per mole of carbon in reaction as previously defined; the conversion in electricity is then 430.661 x 41% = 176.571 kJ elect., i. e. a gain of 38.571 kJ elect., 27.95% more electricity "for the same quantity of carbon as introduced".

[0087] Both processes use a mole of carbon generating a mole of CO₂.

[0088] In a conventional system, this mole of CO₂ is diluted in smokes (in a proportion between 14 and 18% of CO₂ per Nm³) and its collection requires important means.

[0089] In the system and process of the invention, this same mole of CO₂ is not diluted, has a proportion of 98% or more of the exit volume and can be directly collected. This mole of CO₂ can be collected for stocking and/or recycling.

[0090] Figure 2 is a schematic representation of a second way of assembly of a system of the invention.

[0091] The system 200 represented by Figure 2 comprises all the elements of the system 100 as represented by Figure 1.

[0092] The system 200 also comprises a bioreactor containing microalgae.

[0093] The part DFG2 of the second cooled gaseous flow as obtained at the outlet of the feeding chamber 108 of the gasification reactor 102 is injected into the bioreactor 202. In the alga culture bioreactor 202, carbon dioxide CO₂ is used by photosynthesis as performed by microalgae. Photosynthesis produces, on one hand, carbon biomass BC and, on the other hand, a gaseous flow of oxygen FO₂ by separating the carbon element <<C>> from the molecule of dioxygen <<O₂>>.

[0094] The carbon biomass BC as obtained is supplied to a biomass conditioned system 204 which may be:

• a system to extract essential oils from microalgae with high content of lipids and feed-pharmaceutical molecules as used in the pharmacopea and/or hydrocarbons. at the end of that extraction, about 30% of the biomass remain in the form of coal, which may be returned to the gasifier 102;
• or e. g. a drying system to be conditioned before its introduction into the gasification reactor 102.

[0095] The gaseous flow of oxygen FO₂ may be supplied to the system of the invention, e. g. at the level of the gasification reactor 102 to complement gasification of material containing carbon in the reactor 102.

[0096] Advantageously, the production of carbon-containing biomass in this second way of embodiment stimulates thermal yield in the reference evaporator, "delivering" 394 kJ (of the element C as recycled in biomass); the conversion into electricity is then 430.661 + 394 = 824.661 x 41% = 338.111 kJ electric, i. e. a multiplying coefficient of electricity production "by the same mole of carbon as introduced" of 2.45.

[0097] In this example, carbon is oxidized by the molecule of O₂, thus again generating a CO₂ which is recycled in the same fashion. There is no atmospheric rejection or need for depuration.

[0098] The invention is surely not limited to the examples as disclosed.

Claims

1. Process to produce electricity from raw material containing carbon (C), said process comprising at least one iteration of the following steps constituting a treatment cycle:

- a gasification step in a first so-called gasification reactor (102) of dry carbon-containing raw material (C) with a gaseous gasification flow (FGG) comprising CO₂ at high temperature, said gasification step comprising supplying a first gaseous flow (PFG) essentially comprising molecules of carbon monoxide (CO);

- an oxidation step in a second so-called oxidation reactor (104) by oxygen holders in oxide state (MeO) of said molecules of carbon monoxide (CO) as present in said first gaseous flow (PFG), said oxidation step comprising supplying a second gaseous flow (DFG) at high temperature containing CO₂ and oxygen holders in reduced state (Me);

- an activation step in a so-called third activation reactor (106) of said oxygen holders in reduced state (Me) with a so-called gaseous flow of activation (FA), comprising elements of oxygen (O), said activation step comprising supplying oxygen holders in oxide state (MeO) and an oxygen-poor gaseous flow of activation at high temperature (FAA); the process being characterized by:

- a step of transferring a part of the thermal power as generated during gasification to the gaseous oxygen-poor flow of activation (FAA); and

- a conversion step comprising conversion in electricity of at least a part of the thermal power of said gaseous oxygen-poor flow of activation at high temperature (FAA).

2. Process of claim 1, characterized by the fact that the conversion step comprises a step of transfer of at least a part of the thermal power of said gaseous oxygen-poor flow of activation (FAA) to a so-called electricity-generating fluid (FGE) as supplied to a converter device for the production of electricity.

3. Process of claim 1 or 2, characterized by comprising furthermore a recovery of residual thermal power from said gaseous oxygen-poor flow of activation (FAA), being at least a part of said residual thermal power transferred to the gaseous flow of gasification (FGG) as used in the next cycle of treatment.

4. Process of any of claims 1 to 3, characterized by comprising a step of raw material temperature increase containing carbon (C) before the gasification by the transfer of at least one part of the thermal power of the second gaseous flow (DFG) at high temperature to said raw material containing carbon (C).

5. Process of any of claims 1 to 4, characterized by comprising closed circuit recycling of at least a part (DFG1) of CO₂ from the second gaseous flow (DFG) to constitute said gaseous flow of gasification (FGG).

6. Process of claim 2 or of any of claims 3 to 5 when according to claim 2, characterized by comprising, before the step of activation, pre-heating of the gaseous flow of activation (FA) with the residual energy of the electricity generation fluid (FGE).

7. Process of any of claims 5 or 6, characterized by comprising the supply of a part (DFG2) of the second gaseous flow (DFG) to a bioreactor (202) containing microalgae, after the refrigeration of said part (DFG2) of said second gaseous flow (DFG), wherein said microalgae photosynthesize CO₂ as present in said part (DFG2) of said second gaseous flow (DFG), said bioreactor (202) supplies, on one hand, a gaseous flow of oxygen (FO₂) and, on the other hand, carbon biomass (BC).

8. Process of claim 7, characterized by comprising the recovery and treatment of the carbon biomass (BC) as supplied by the bioreactor (202), considering the gasification of said biomass (BC) in the gasification reactor (102).

9. Process of any of claims 7 or 8, characterized by comprising the recovery of at least a part of the gaseous flow of oxygen (FO₂) as generated by microalgae and an injection of at least a part of said flow of oxygen (FO₂) in the gasification reactor (102) to complement the gasification of the raw material containing carbon (C).

10. System (100, 200) for production of electricity from dry raw material of carbon (C), said system comprising:

- a gasification reactor (102) for gasification of carbon-containing raw material (C) with a gaseous flow of gasification (FGG) comprising CO₂ at high temperature, said reactor (102) supplying a first gaseous flow (PFG) comprising molecules of carbon monoxide (CO);

- an oxidation reactor (104) for oxidation by oxygen holders in oxide state (MeO) of said molecules of carbon monoxide (CO) as present in said first gaseous flow (PFG), said oxidation reactor supplying a second gaseous flow (DFG) at high temperature comprising CO₂ and oxygen holders in reduced state (Me);

- an activation reactor (106) for activation of said holders of oxygen in reduced state (Me) with a gaseous flow (FA) comprising elements of oxygen (O), said reactor (106) supplying holders of oxygen in oxide state (MeO) and an excess of thermal power; characterized in that said system further comprises:

- means for transferring a part of the thermal power as generated during gasification to the gaseous oxygen-poor flow of activation (FAA);

- an electricity generation device (114) from at least a part of said thermal excess from said activation reactor.

11. System of claim 10, characterized by containing mechanical means of transportation of the oxygen holders from the oxidation reactor to the activation reactor and/or from the activation reactor to the oxidation reactor.

12. System of any of claims 10 or 11, characterized by comprising a closed ring recycling circuit for recycling a part (DFG1) of the CO₂ as present in the second gaseous flow (DFG) as the gaseous flow of gasification (FGG).

13. System of any of claims 10 to 12, characterized by the electricity generator device containing a turboalternator (114).

14. System of any of claims 10 to 13, characterized by comprising a bioreactor (202) containing microalgae to which a part (DFG2) of the CO₂ as present in the second gaseous flow (DFG) is supplied, wherein said microalgae photosynthesize said CO₂, said bioreactor (202) supplying, on one hand, a gaseous flow of oxygen (FO₂) and, on the other hand, carbon biomass (BC).

Ansprüche

1. Verfahren zur Erzeugung von Elektrizität aus Kohlenstoff (C) enthaltendem Rohmaterial, wobei das besagte Verfahren aus mindestens einer Iteration der folgenden Schritte eines Behandlungskreislaufs besteht.

- einem Vergasungsschritt von trockenem Kohlenstoff (C) enthaltendem Rohmaterial in einem ersten so genannten Vergasungsreaktor (102) mit einem gasförmigem Vergasungsstrom (FGG), bestehend aus CO₂ bei hoher Temperatur, wobei der besagte Vergasungsschritt einen ersten Gasstrom (PFG) von wesentlich aus Kohlenmonoxid (CO) bestehenden Molekülen liefert.

- einem Oxidationsschritt der besagten, im ersten Gasstrom (PFG) enthaltenen Kohlenmonoxid (CO) Moleküle in einem zweiten so genannten Oxidationsreaktor (104) durch Sauerstoffträger im Oxidzustand (MeO), wobei der besagte Oxidationsschritt aus der Lieferung eines zweiten Gasstroms (DFG) bei hoher Temperatur besteht, der CO₂ und Sauerstoffträger in reduziertem Zustand (Me) enthält.

- einem Aktivierungsschritt der besagten Sauerstoffträger in reduziertem Zustand (Me) in einem so genannten dritten Aktivierungsreaktor (106) mit einem so genannten, aus Sauerstoffelementen (O) bestehenden, gasförmigen Aktivierungsstrom (FA), wobei der besagte Aktivierungsschritt aus der Lieferung von Sauerstoffträgern im Oxidzustand (MeO) und einem sauerstoffarmen gasförmigen Aktivierungsstrom (FAA) bei hoher Temperatur besteht. Das Verfahren ist gekennzeichnet durch:

- einen Übertragungsschritt eines Teils der während der Vergasung erzeugten Wärmeenergie auf den sauerstoffarmen gasförmigen Aktivierungsstrom (FAA) und

- einen Konvertierungsschritt, bestehend aus der Konvertierung mindestens eines Teils der Wärmeenergie des besagten sauerstoffarmen gasförmigen Aktivierungsstrom (FAA) bei hoher Temperatur in Elektrizität.

2. Verfahren gemäß Anspruch 1, gekennzeichnet durch die Tatsache, dass der Konvertierungsschritt einen Schritt der Übertragung mindestens eines Teils der Wärmeenergie des besagten sauerstoffarmen gasförmigen Aktivierungsstrom (FAA) auf eine so genannte Elektrizität-erzeugende Flüssigkeit (FGE) enthält, die einer Konvertereinheit zur Erzeugung von Elektrizität zugeführt wird.

3. Verfahren gemäß Anspruch 1 oder 2, dadurch gekennzeichnet, dass es zudem aus einer Rückgewinnung der restlichen Wärmeenergie aus dem besagten sauerstoffarmen gasförmigen Aktivierungsstrom (FAA) besteht, wobei mindestens ein Teil der besagten restlichen Wärmeenergie auf den gasförmigem, im nächsten Behandlungszyklus verwendeten Vergasungsstrom (FGG) übertragen wird.

4. Verfahren gemäß einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass es einen Schritt der Temperaturerhöhung des Kohlenstoff (C) enthaltenden Rohmaterials vor der Vergasung enthält, durch die Übertragung mindestens eines Teils der Wärmeenergie des zweiten Gasstroms (DFG) bei hoher Temperatur auf das besagte, Kohlenstoff (C) enthaltende Rohmaterial.

5. Verfahren gemäß einem der Ansprüche 1 bis 4, gekennzeichnet durch das Recycling mindestens eines Teils (DFG1) des CO₂ aus dem zweiten Gasstrom (DFG) im geschlossenen Kreislauf, um den besagten gasförmigen Vergasungsstrom (FGG) zu bilden.

6. Verfahren gemäß Anspruch 2 oder einem der Ansprüche 3 bis 5, wenn gemäß Anspruch 2, dadurch gekennzeichnet, dass vor dem Aktivierungsschritt eine Vorwärmung des gasförmigen Aktivierungsstrom (FA) mit der Restenergie aus der Elektrizität-erzeugende Flüssigkeit (FGE) erfolgt.

7. Verfahren gemäß einem der Ansprüche 5 oder 6, gekennzeichnet durch die Lieferung eines Teils (DFG2) des zweiten Gasstroms (DFG) an einen, Mikroalgen enthaltenden Bioreaktor (202) nach der Abkühlung des besagten Teils (DFG2) des besagten zweiten Gasstroms (DFG), worin die besagten Mikroalgen eine Photosynthese des im besagten Teil (DFG2) vorhandenen CO₂ des besagten zweiten Gasstroms (DFG) durchführen, wobei der besagte Bioreaktor (202) einerseits einen gasförmigen Sauerstoffstrom (FO₂) und andererseits eine Kohlenstoff-Biomasse (BC) liefert.

8. Verfahren gemäß Anspruch 7, gekennzeichnet durch die Rückgewinnung und Behandlung der vom Bioreaktor (202) bereitgestellten Kohlenstoff-Biomasse (BC) unter Berücksichtigung der Vergasung der besagten Biomasse (BC) im Vergasungsreaktor (102).

9. Verfahren gemäß einem der Ansprüche 7 oder 8, gekennzeichnet durch die Rückgewinnung mindestens eines Teils des, von den Mikroalgen erzeugten, gasförmigen Sauerstoffstroms (FO₂) und der Injektion von mindestens einem Teil des besagten Sauerstoffstroms (FO₂) in den Vergasungsreaktor (102), um die Vergasung des Kohlenstoff (C) enthaltenden Rohmaterials zu ergänzen.

10. System (100, 200) zur Erzeugung von Elektrizität aus trockenem, aus Kohlenstoff bestehendem Rohmaterial (C), wobei das besagte System folgendes beinhaltet:

- einen Vergasungsreaktor (102) für die Vergasung von Kohlenstoff (C) enthaltendem Rohmaterial mit einem gasförmigem Vergasungsstrom (FGG), bestehend aus CO₂ bei hoher Temperatur, wobei der besagte Reaktor (102) einen ersten Gasstrom (PFG) von aus Kohlenmonoxid (CO) bestehenden Molekülen liefert.

- einen Oxidationsreaktor (104) zur Oxidation der besagten, im ersten Gasstrom (PFG) enthaltenen Kohlenmonoxid (CO) Moleküle durch Sauerstoffträger im Oxidzustand (MeO), wobei der besagte Oxidationsreaktor einen zweiten Gasstrom (DFG) bei hoher Temperatur liefert, der CO₂ und Sauerstoffträger in reduziertem Zustand (Me) enthält.

- einen Aktivierungsreaktor (106) zur Aktivierung der besagten Sauerstoffträger in reduziertem Zustand (Me) mit einem aus Sauerstoffelementen (O) bestehenden Gasstrom (FA), wobei der besagte Reaktor (106) Sauerstoffträger im Oxidzustand (MeO) und einen Überschuss von Wärmeenergie liefert, dadurch gekennzeichnet, dass das besagte System weiterhin folgendes beinhaltet:

- Mittel zur Übertragung eines Teils der während der Vergasung erzeugten Wärmeenergie auf den sauerstoffarmen gasförmigen Aktivierungsstrom (FAA);

- ein Gerät zur Erzeugung von Elektrizität (114) aus mindestens einem Teil des besagten Wärmeüberschusses aus dem besagten Aktivierungsreaktor.

11. System gemäß Anspruch 10, dadurch gekennzeichnet, dass es mechanische Transportmittel für die Sauerstoffträger vom Oxidationsreaktor zum Aktivierungsreaktor und/oder vom Aktivierungsreaktor zum Oxidationsreaktor enthält.

12. System gemäß einem der Ansprüche 10 oder 11, gekennzeichnet durch einen geschlossenen Recycling-Kreislauf für das Recycling eines Teils (DFG1) des CO₂ aus dem zweiten Gasstrom (DFG), als den gasförmigen Vergasungsstrom (FGG).

13. System gemäß einem der Ansprüche 10 bis 12, dadurch gekennzeichnet, dass das Stromerzeugungsgerät (114) einen Turbogenerator enthält.

14. System gemäß einem der Ansprüche 10 bis 13, gekennzeichnet durch einen Mikroalgen enthaltenden Bioreaktor (202), an welchen ein Teil (DFG2) des im zweiten Gasstrom (DFG) vorhandenen CO₂ geliefert wird, worin die besagten Mikroalgen eine Photosynthese des besagten CO₂ durchführen, wobei der besagte Bioreaktor (202) einerseits einen gasförmigen Sauerstoffstrom (FO₂) und andererseits eine Kohlenstoff-Biomasse (BC) liefert.

Revendications

1. Process to produce electricity from raw material containing carbon (C), said process comprising at least one itération of the following steps constituting a treatment cycle:
Procédé de production d'électricité à partir de matière première contenant du carbone (C), ledit procédé comprenant au moins une itération des étapes suivantes constituant un cycle de traitement:

- a gasification step in a first so-called gasification reactor (102) of dry carboncontaining raw material (C) with a gaseous gasification flow (FGG) comprising CO2 at high temperature, said gasification step comprising supplying a first gaseous flow (PFG) essentially comprising molecules of carbon monoxide (CO);
une étape de gazéification dans un premier réacteur dit de gazéification (102) de matière première sèche contenant du carbone (C) avec un flux gazeux de gazéification (FGG) comprenant du CO2 à haute température, ladite étape de gazéification comprenant la fourniture d'un premier flux gazeux (PFG) comprenant essentiellement des molécules de monoxyde de carbone (CO);

- an oxidation step in a second so-called oxidation reactor (104) by oxygen holders in oxide state (MeO) of said molecules of carbon monoxide (CO) as present in said first gaseous flow (PFG), said oxidation step comprising supplying a second gaseous flow (DFG) at high temperature containing C02 and oxygen holders in reduced state (Me);
une étape d'oxydation dans un deuxième réacteur dit d'oxydation (104) par des porteurs d'oxygène à l'état d'oxyde (MeO) desdites molécules de monoxyde de carbone (CO) présentes dans ledit premier flux gazeux (PFG), ladite étape d'oxydation comprenant la fourniture d'un second flux gazeux (DFG) à haute température contenant du CO2 et des porteurs d'oxygène à l'état réduit (Me);

- an activation step in a so-called third activation reactor (106) of said oxygen holders in reduced state (Me) with a so-called gaseous flow of activation (FA), comprising elements of oxygen (0), said activation step comprising supplying oxygen holders in oxide state (MeO) and an oxygen-poor gaseous flow of activation at high temperature (FAA);
the process being characterized by:

une étape d'activation dans un troisième réacteur dit d'activation (106) desdits porteurs d'oxygène à l'état réduit (Me) avec un flux dit d'activation gazeuse (FA), comprenant des éléments d'oxygène (0), ladite étape d'activation comprenant la fourniture des porteurs d'oxygène à l'état d'oxyde (MeO) et un flux gazeux d'activation à haute température (FAA) appauvri en oxygène;

le processus étant caractérisé par:

- a step of transferring a part of the thermal power as generated during gasification to the gaseous oxygen-poor flow of activation (FAA); and une étape de transfert d'une partie de la puissance thermique générée lors de la gazéification vers le flux gazeux d'activation pauvre en oxygène (FAA); et

- a conversion step comprising conversion in electricity of at least a part of the thermal power of said gaseous oxygen-poor flow of activation at high temperature (FAA).
une étape de conversion comprenant la conversion en électricité d'au moins une partie de la puissance thermique dudit flux gazeux d'activation à haute température pauvre en oxygène (FAA).

2. Process of claim 1, characterized by the fact that the conversion step comprises a step of transfer of at least a part of the thermal power of said gaseous oxygen-poor flow of activation (FAA) to a so-called electricity-generating fluid (FGE) as supplied to a converter device for the production of electricity.
Procédé selon la revendication 1, caractérisé par le fait que l'étape de conversion comprend une étape de transfert d'au moins une partie de la puissance thermique dudit flux gazeux d'activation appauvri en oxygène (FAA) vers un fluide (FGE), dit générateur d'électricité, fourni à un dispositif de convertisseur pour la production d'électricité.

3. Process of claim 1 or 2, characterized by comprising furthermore a recovery of residual thermal power from said gaseous oxygen-poor flow of activation (FAA), being at least a part of said residual thermal power transferred to the gaseous flow of gasification (FGG) as used in the next cycle of treatment. Procédé selon la revendication 1 ou 2, caractérisé en ce qu'il comprend en outre une récupération de la puissance thermique résiduelle à partir dudit flux d'activation pauvre en oxygène gazeux (FAA), au moins une partie de ladite énergie thermique résiduelle étant transférée au flux gazeux de gazéification (FGG) utilisé dans le cycle de traitement suivant.

4. Process of any of claims 1 to 3, characterized by comprising a step of raw material temperature increase containing carbon (C) before the gasification by the transfer of at least one part of the thermal power of the second gaseous flow (DFG) at high temperature to said raw material containing carbon (C). Procédé selon l'une quelconque des revendications 1 à 3, caractérisé en ce qu'il comprend une étape d'augmentation de la température de la matière première contenant du carbone (C), avant la gazéification, par transfert d'au moins une partie de la puissance thermique du deuxième flux gazeux (DFG) à haute température à ladite matière première contenant du carbone (C).

5. Process of any of claims 1 to 4, characterized by comprising closed circuit recycling of at least a part (DFG1) of CO2 from the second gaseous flow (DFG) to constitute said gaseous flow of gasification (FGG).
Procédé selon l'une quelconque des revendications 1 à 4, caractérisé en ce qu'il comprend le recyclage en circuit fermé d'au moins une partie (DFG1) du CO2 du deuxième flux gazeux (DFG) pour constituer ledit flux gazeux de gazéification (FGG).

6. Process of claim 2 or of any of claims 3 to 5 when according to claim 2 characterized by comprising, before the step of activation, pre-heating of the gaseous flow of activation (FA) with the residual energy of the electricity generation fluid (FGE).
Procédé selon la revendication 2 ou l'une quelconque des revendications 3 à 5 lorsque selon la revendication 2 caractérisé en ce qu'il comprend, avant l'étape d'activation, un préchauffage du flux gazeux d'activation (FA) avec l'énergie résiduelle du fluide de génération d'électricité (FGE).

7. Process of any of claims 5 or 6, characterized by comprising the supply of a part (DFG2) of the second gaseous flow (DFG) to a bioreactor (202) containing microalgae, after the réfrigération of said part (DFG2) of said second gaseous flow (DFG), wherein said microalgae photosynthesize CO2 as present in said part (DFG2) of said second gaseous flow (DFG), said bioreactor (202) supplies, on one hand, a gaseous flow of oxygen (FO2) and, on the other hand, carbon biomass (BC).
Procédé selon l'une quelconque des revendications 5 ou 6, caractérisé en ce qu'il comprend la fourniture d'une partie (DFG2) du deuxième flux gazeux (DFG) à un bioréacteur (202) comprenant des microalgues, après refroidissement de ladite partie (DFG2) dudit second gazeux (DFG), lesquelles microalgues photosynthétisent le CO2 présent dans ladite partie (DFG2) dudit deuxième flux gazeux (DFG), ledit bioréacteur (202) fournit, d'une part, un flux gazeux d'oxygène (FO2) et, d'autre part, de la biomasse carbonée (BC).

8. Process of claim 7, characterized by comprising the recovery and treatment of the carbon biomass (BC) as supplied by the bioreactor (202), considering the gasification of said biomass (BC) in the gasification reactor (102).
Procédé selon la revendication 7, caractérisé en ce qu'il comprend la récupération et le traitement de la biomasse carbonée (BC) fournie par le bioréacteur (202), en vue de la gazéification de ladite biomasse (BC) dans le réacteur de gazéification (102).

9. Process of any of claims 7 or 8 characterized by comprising the recovery of at least a part of the gaseous flow of oxygen (FO2) as generated by microalgae and an injection of at least a part of said flow of oxygen (FO2) in the gasification reactor (102) to complement the gasification of the raw material containing carbon (C).
Procédé selon l'une quelconque des revendications 7 ou 8, caractérisé en ce qu'il comprend la récupération d'au moins une partie du flux gazeux d'oxygène (FO2) généré par les microalgues et une injection d'au moins une partie dudit flux d'oxygène (FO2) dans le réacteur de gazéification (102) pour complémenter la gazéification de la matière première carbonée (C).

10. System (100, 200) for production of electricity from dry raw material of carbon (C), said system comprising:
Système (100, 200) pour la production d'électricité à partir de matière première sèche contenant du carbone (C), ledit système comprenant:

- a gasification reactor (102) for gasification of carbon-containing raw material (C) with a gaseous flow of gasification (FGG) comprising CO2 at high temperature, said reactor (102) supplying a first gaseous flow (PFG) comprising molecules of carbon monoxide (CO);
un réacteur de gazéification (102) pour la gazéification de la matière première contenant du carbone (C) avec un flux gazeux de gazéification (FGG) comprenant du CO2 à haute température, ledit réacteur (102) fournissant un premier flux gazeux (PFG) comprenant des molécules de monoxyde de carbone (CO);

- an oxidation reactor (104) for oxidation by oxygen holders in oxide state (MeO) of said molecules of carbon monoxide (CO) as present in said first gaseous flow (PFG), said oxidation reactor supplying a second gaseous flow (DFG) at high temperature comprising CO2 and oxygen holders in reduced state (Me);
un réacteur d'oxydation (104) pour l'oxydation par des porteurs d'oxygène à l'état d'oxyde (MeO) desdites molécules de monoxyde de carbone (CO) présentes dans ledit premier flux gazeux (PFG), ledit réacteur d'oxydation fournissant un second flux gazeux (DFG) à haute température comprenant du CO2 et des porteurs d'oxygène à l'état réduit (Me);

- an activation reactor (106) for activation of said holders of oxygen in reduced state (Me) with a gaseous flow (FA) comprising elements of oxygen (0), said reactor (106) supplying holders of oxygen in oxide state (MeO) and an excess of thermal power; characterized in that said system further comprises:

un réacteur d'activation (106) pour l'activation desdits détenteurs d'oxygène à l'état réduit (Me) avec un flux gazeux (FA) comprenant des éléments d'oxygène (0), ledit réacteur (106) fournissant des détenteurs d'oxygène à l'état d'oxyde (MeO) et un excès de puissance thermique;

caractérisé en ce que ledit système comprend en outre:

- means for transferring a part of the thermal power as generated during gasification to the gaseous oxygen-poor flow of activation (FAA); des moyens pour transférer une partie de la puissance thermique générée pendant la gazéification vers le flux gazeux d'activation pauvre en oxygène (FAA);

- an electricity generation device (114) from at least a part of said thermal excess from said activation reactor.
un dispositif de génération d'électricité (114) à partir d'au moins une partie dudit excès thermique dudit réacteur d'activation.

11. System of claim 10, characterized by containing mechanical means of transportation of the oxygen holders from the oxidation reactor to the activation reactor and/or from the activation reactor to the oxidation reactor.
Système selon la revendication 10, caractérisé par le fait qu'il contient des moyens mécaniques de transport des porteurs d'oxygène du réacteur d'oxydation au réacteur d'activation et/ou du réacteur d'activation au réacteur d'oxydation.

12. System of any of claims 10 or 11, characterized by comprising a closed ring recycling circuit for recycling a part (DFG1) of the CO2 as present in the second gaseous flow (DFG) as the gaseous flow of gasification (FGG). Système selon l'une quelconque des revendications 10 ou 11, caractérisé en ce qu'il comprend un circuit de recyclage en circuit fermé pour recycler une partie (DFG1) du CO2 présent dans le deuxième flux gazeux (DFG) en tant que flux gazeux de gazéification (FGG).

13. System of any of claims 10 to 12, characterized by the electricity generator device containing a turboalternator (114).
Système selon l'une quelconque des revendications 10 à 12, caractérisé par le dispositif générateur d'électricité comprenant un turboalternateur (114).

14. System of any of claims 10 to 13, characterized by comprising a bioreactor (202) containing microalgae to which a part (DFG2) of the CO2 as present in the second gaseous flow (DFG) is supplied, wherein said microalgae photosynthesize said CO2, said bioreactor (202) supplying, on one hand, a gaseous flow of oxygen (FO2) and, on the other hand, carbon biomass (BC). Système selon l'une quelconque des revendications 10 à 13, caractérisé en ce qu'il comprend un bioréacteur (202) contenant des microalgues auquel est fournie une partie (DFG2) du CO2 présent dans le deuxième flux gazeux (DFG), dans lequel les microalgues photosynthétisent ledit CO2, ledit bioréacteur (202) fournissant, d'une part, un flux gazeux d'oxygène (FO2) et, d'autre part, de la biomasse carbonée (BC).

Drawing