Patent Application
20230070109
The present invention relates to a device as well as a system and a method for storage of energy and carbon capture, where a storage compartment is transportable.
WO 2012/118437 discloses a particle comprising an inner part and an outer coating, said inner part comprises at least one selected from the group consisting of a salt and CaO and said outer coating comprises hydrophobic nanoparticles.
WO 2016/166364 discloses a material for use in a chemical heat pump, the material comprises an active substance, and allows transport of a volatile liquid in gas phase to and from at least a part of the active substance, wherein at least a part of the material is in thermal contact with the surroundings, where the material comprises flakes of at least one selected from the group consisting of graphene and graphene oxide, wherein each individual flake has a lateral size in the range 100-10000 nm and a thickness in the range 0.34 to 5 nm.
EP2762781 discloses using a CaO/CaCO3 loop for CO2 capture from flue gases (CCS) by means of fluidized bed technology. Energy storage using CaO/CaCO3 in conjunction with CO2 capture is described. A solution is provided to uncouple the power output from the operation conditions of an oxyfired circulating fluidized bed calciner to be able to operate with different power outputs.
US 2018/0028967 discloses collection of CO2 with CaO in combination with a process for cement manufacture. WO2009144472 discloses removal (CaO/CaCO3) of CO2 from exhaust gases using fluidised bed reactors. The carbon dioxide acceptor (e.g. CaO) is nanoparticulate and coated with a metal oxide (e.g. SiO2). It is mentioned that the metal oxides can be nanostructured and that this can stabilize pore structure which is present when the carbon dioxide acceptor is nanoparticulate. But also mention that the problem of agglomeration still is present, in spite of nanostructures.
US20120025134 relates to CCS with CaO/CaCO3 and in particular to a method of producing a CO2 adsorbent. Mentions that the incorporation of CaO into an inert porous metal oxide produces a sorbent with desirable properties. CaO crystals or grains may be about 150 nm in diameter, while MgO grains that separate them may be about 30 nm in diameter. The mixture is produced by mixing a CaO with at least one metal oxide in a solvent. The metal oxide may be silicon oxide or others.
US 2014/0044632 discloses a device for collection of CO2 from exhaust gas from a vehicle, a heating system or in industrial process. The focus of the application is absorption of CO2. All absorbent is all the time in the absorber cartridge so that the gases are lead through the entire or a large portion of the absorbent. This has the effect that the absorption rate for CO2 decreases non-linearly, which is a disadvantage for energy storage purposes. The absorbent is lime and specifically soda lime comprising CaOH with a smaller part of NaOH and KOH.
Known systems for carbon capture and energy storage using CaO/CaCO3 typically comprise a carbonator and a calciner. Problems in the prior art include that the calciner is a complex device which is more complicated than the carbonator and that the calciner is easier to build in large or very large scale. The carbonator on the other hand is scalable for instance because it has fewer components and no filters. The carbonator can be made in any desirable size including very small sizes.
It is also desirable to minimize the long-term structural changes and agglomeration in CaO/CaCO3, which may occur during repeated cycles.
One objective of the present invention is to obviate at least some of the disadvantages in the prior art and provide an energy storage system as well as a method.
In a first aspect there is provided a system for energy storage and CO2 capture comprising:
In a second aspect there is provided a method for storing energy and capturing CO2 comprising the steps of:
Further embodiments of the present invention are defined in the appended dependent claims, which are explicitly incorporated herein.
It is an advantage that the capacity of the carbonator can be adapted to the need at the location where it is installed. The capacity of the carbonator is easy to adapt form a technical point of view. The calciner which is more difficult to manufacture in small scale can be made large and serve many carbonators.
The release of heat in the carbonator and the corresponding heat consumption in the calciner can be used as an energy storage. The calciner can be operated at hours when the energy cost is lower. The device releasing CO2 normally operates when there is a need for energy and then the carbonator is active giving an additional boost.
Aspects and embodiments will be described with reference to the following drawing in which:
Before the invention is disclosed and described in detail, it is to be understood that this invention is not limited to particular configurations, process steps and materials disclosed herein as such configurations, process steps and materials may vary somewhat. It is also to be understood that the terminology employed herein is used for the purpose of describing particular embodiments only and is not intended to be limiting since the scope of the present invention is limited only by the appended claims and equivalents thereof.
It must be noted that, as used in this specification and the appended claims, the singular forms “a”, “an” and “the” include plural referents unless the context clearly dictates otherwise.
“Energy storage” as used throughout the description and in the claims denote the storage of energy including storage of energy in chemical form and also storage of energy as heat energy, including storage in phase change materials.
“Largest size” of a volume or particle as used throughout the description and in the claims denote the largest distance between any two points on the surface of the volume or particle. Of all possible distances between two arbitrary points on the surface of the particle or volume, the largest possible distance is selected. For a sphere this corresponds to the diameter of the sphere.
“Particle” as used throughout the description and in the claims denote a piece of material in solid form.
“System” as used throughout the description and in the claims denote a combination of several devices.
In a first aspect there is provided a system for energy storage and CO2 capture comprising:
The CaCO3 storage container (2) is configured to be transportable so that it can be connected to, pulled along by or loaded into some kind of transportation device such as a truck, a cargo train or a boat.
The CaCO3 is intended to be supplied to a geographical location (3) remote from the carbonator (1) for CO2 release. A geographical location (3) remote from the carbonator (1) is at another place, examples include but are not limited to at least 1 km away from the carbonator (1), and at least 10 km away from the carbonator (1). Thus in one embodiment the geographical location (3) remote from the carbonator (1) is 1 km or more away from the carbonator (1). A geographical location (3) remote from the carbonator (1) is to be interpreted so that the distance is so that the CaCO3 storage container (2) should be transportable and so that it is not economically realistic to have another transportation means for the CaCO3, such as for instance a conveyor belt or a pipe. A remote geographical location is located as such a distance that a transportable storage container suitably is used. As an alternative this distance is at least 1 km, alternatively at least 10 km. The captured CO2 is released at the geographical location (3).
In the art, it is a problem that calciner are not very scalable and difficult to build in small scale. This is due to their complexity including many components and filters. Calciners are from a technical point of view easier to build in large scale. Carbonators on the other hand are much more scalable compared to calciners. Carbonators can more easily be made in small scale and the size and capacity of the carbonator can then be adapted to the need at the site where CO2 capture is needed.
Heat is released in the carbonator and the corresponding heat is consumed in the calciner. This is suitably used as an energy storage so that the carbonator gives an additional heat boost during operation. The calciner can be operated at hours when the energy cost is lower. Thereby an energy storing effect is achieved consuming energy when available and releasing heat energy when there is a need. The device releasing CO2 normally operates when there is a need for energy and then the carbonator is active giving an additional boost.
The CO2 which is captured can come from various sources, examples include but are not limited to flue gas and exhaust gas from combustion. Before the CO2 is captured the gas is preferably treated in filters and separators to remove for instance particulates, sulphur compounds and similar. Such filtration steps and separation steps before CO2 removal are known in the art.
In one embodiment the system further comprises
The CaCO3 storage containers (2) and the CaO storage containers (5) are not necessarily different, in one embodiment the same type of containers are utilized for both purposes.
In one embodiment, the CaO is coated with particles comprising SiO2, and wherein the particles comprising SiO2 have a diameter in the range 1-100 nm. In one embodiment the CaO and CaCO3 is coated with particles comprising SiO2, and wherein the particles comprising SiO2 have a diameter in the range 1-100 nm. In one embodiment hydrophobized SiO2 is used. For irregular particles the diameter should be interpreted as the largest size in any dimension. During repeated use of the material CaO/CaCO3 long term effects may occur including formation of crystals and other structural changes which impairs the reactivity of the material. The coating with particles comprising SiO2 ameliorates this problem. Further the coating makes the material easier to transport and handle since it flows easier. The coating comprises a layer of SiO2− particles on the surface of the particles of CaO/CaCO3. The coating is permeable to CO2. When the material in the particles change from CaO to CaCO3 and vice versa there is typically a volume change, but the coating of particles is able to adapt to the new volume of the particles as the material in the core changes between CaO and CaCO3. The particles of CaO/CaCO3 are larger than the particles comprising SiO2, in one embodiment 100-1000 times larger.
Both the CaO and/or the CaCO3 are provided in the form of particles. In one embodiment, the particles comprising CaO and/or CaCO3 have a largest size in the range 1-1000 μm. The largest size in the largest size measured in any dimension. For a sphere the largest size corresponds to the diameter.
In one embodiment, the calciner (4) has a capacity to produce CaO per hour, which is at least 4 times larger than the capacity of the carbonator (1) to consume CaO per hour, calculated by weight. In yet another embodiment the calciner (4) has a capacity to produce CaO per hour, which is at least 10 times larger than the capacity of the carbonator (1) to consume CaO per hour, calculated by weight. In one embodiment, there is a plurality of carbonators (1). This has the advantage that one calciner can serve several carbonators and that the carbonator can be adapted to the needed capacity at each location and that the capacity of the calciner can be optimally designed which is a large calciner.
In one embodiment the carbonator (1) and calciner (4) are located at least 1 km apart. In another embodiment the the carbonator (1) and calciner (4) are located at least 0.5 km apart. In another embodiment the carbonator (1) and calciner (4) are located at least 5 km apart. In another embodiment the carbonator (1) and calciner (4) are located at least 10 km apart.
In one embodiment wherein there are more carbonators (1) than calciners (4).
In one embodiment, the transportable CaCO3 storage container (2) comprises lifting means (6) for lifting and moving the transportable CaCO3 storage container (2). The lifting means (6) can be any known feature allowing the container to be lifted and/or moved. Examples of lifting means include but are not limited to a hook, a loop, a handle, a flange, and a groove.
In one embodiment the transportable CaCO3 storage container (2) comprises CaCO3 container input means (7) for connecting the transportable CaCO3 storage container (2) to the carbonator (1) for supply of CaCO3 from the carbonator (1) to the CaCO3 storage container (2), preferably in the form of quick-release input connection means (7). A quick-release input connection can be released at short time and can be reused during many operation cycles. In one embodiment the CaCO3 container input means (7) is an opening in the top of the CaCO3 storage container (2).
In one embodiment the carbonator (1) comprises carbonator CaCO3 output means (8) for connecting the carbonator (1) to the CaCO3 container input means (7) of the transportable CaCO3 storage container (2) for supply of CaCO3 from the carbonator (1) to the CaCO3 storage container (2).
In one embodiment, the transportable CaCO3 storage container (2) comprises CaCO3 container output means (9) for connecting the transportable CaCO3 storage container (2) to the calciner (4) for supply of CaCO3 in the transportable CaCO3 storage container (2) to the calciner (4).
In a second aspect, there is provided a method for storing energy and capturing CO2 comprising the steps of:
The CO2 provided in step b) is provided from any stream comprising CO2, preferably from a stream comprising an increased concentration of CO2 such as at least 10 wt %, preferably at least 15 wt % or higher. The CO2 can originate form an industrial process generating CO2 including for instance combustion of a carbon containing fuel.
In one embodiment, the method further comprises the steps of:
In one embodiment, the method further comprises the steps of:
Thereby the loop is closed so that the material CaO/CaCO3. can be recycled.
In one embodiment of the method it further comprises the step of storing the CO2 produced in step f. The CO2 can be stored in the bedrock including bedrock comprising lime. Over the years, most of the CO2 will then mineralize and stay in the bedrock.
The embodiments of the system are also applicable to the method.
In one embodiment of the method step d involves transporting more than 1 km.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2050076-5 | Jan 2020 | SE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/051210 | 1/20/2021 | WO |
