selective solar absorbent coating and manufacturing method, with solar absorption and low emissivity properties. The coating comprises a substrate (1) of metal, dielectric or ceramic material, at least one highly reflective metal layer (2) in mid-far infrared applied to the substrate itself which provides low emissivity properties, a multi-layer structure of alternating dielectric and metallic layers (3) of subnanometric thickness applied to the reflective metal layer and at least one dielectric layer (4) that acts as an anti-reflective layer for the solar spectrum. The coating is applicable as a selective absorbent coating in absorbent tubes for parabolic-trough solar collectors, in solar panels for hot water, heating or domestic cooling, both in the form of absorbent tubes and absorbent sheets, in capture systems in tower solar thermoelectric power plants, and in capture systems in Stirling disk systems.
|
3. A solar selective absorbing coating for coating a metallic, dielectric, or ceramic substrate, the solar selective absorbing coating comprising:
at least one reflecting metallic layer deposited on the substrate, the reflecting metallic layer being highly reflective in medium-far infrared; and
an absorbing multilayer structure deposited on the reflecting metallic layer, the absorbing multilayer structure comprising more than 10 dielectric layers alternating with more than 10 metal layers, each of the dielectric and metal layers being less than 10 nm thick; and
at least one anti-reflecting layer deposited on the absorbing multilayer structure; #10#
wherein the total thickness of the coating is between 5 nm and 1000 nm;
and wherein the dielectric layers of the absorbing multilayer structure are made of SiAlOx and the metal layers of the absorbing multilayer structure are made of a metal selected from the group consisting of molybdenum and nickel.
2. A solar selective absorbing coating with solar absorbing properties and low emissivity, comprising:
a substrate of metallic, dielectric or ceramic material;
at least one reflecting metallic layer, which is highly reflective in medium-far infrared, deposited on the substrate; and
an absorbing multilayer structure deposited on the reflecting metallic layer, wherein the absorbing multilayer is not a cermet, the absorbing multilayer structure being composed by alternating dielectric and metal layers; and at least one anti-reflecting dielectric layer deposited on the absorbing multilayer structure, wherein the dielectric layers of the absorbing multilayer structure can be of equal or different thickness and/or composition with respect to each other, the metal layers of the absorbing multilayer structure can have equal or different thickness and/or composition with respect to each other, the thickness of each of the metal and dielectric layers of the absorbing multilayer structure being less than 10 nm, and the overall thickness of the absorbing multilayer structure being between 5 and 1000 nm, and wherein the layers of a dielectric nature of the solar selective absorbing coating are deposited by means of reactive sputtering including inert gas and reactant gas in the chamber or part of the chamber where these dielectric layers are deposited, while the metallic layers of the solar selective absorbing coating are deposited by DC sputtering, introducing inert gas exclusively in the chamber or part of the chamber where these metallic layers are deposited; #10#
wherein:
the absorbing multilayer structure has a homogeneous area with dielectric layers of equal composition and thickness, and metal layers of equal composition and thickness,
the absorbing multilayer structure has two or more homogeneous areas so that the dielectric layers differ in material and/or thickness from one area to another, and the metal layers differ in material and/or thickness from one area to the other area,
the substrate includes stainless steel;
the reflecting metallic layer includes nickel (Ni);
the first homogeneous area of the multilayer structure includes alternating layers of silicon and aluminium oxide (SiAlOx) and Ni;
the second homogeneous area of the multilayer structure includes alternating layers of SiAlOx and Ni; and
the anti-reflecting dielectric layer includes SiAlOx.
1. A solar selective absorbing coating with solar absorbing properties and low emissivity, comprising:
a substrate of metallic, dielectric or ceramic material;
at least one reflecting metallic layer, which is highly reflective in medium-far infrared, deposited on the substrate; and
an absorbing multilayer structure deposited on the reflecting metallic layer, wherein the absorbing multilayer is not a cermet, the absorbing multilayer structure being composed by alternating dielectric and metal layers; and at least one anti-reflecting dielectric layer deposited on the absorbing multilayer structure, wherein the dielectric layers of the absorbing multilayer structure can be of equal or different thickness and/or composition with respect to each other, the metal layers of the absorbing multilayer structure can have equal or different thickness and/or composition with respect to each other, the thickness of each of the metal and dielectric layers of the absorbing multilayer structure being less than 10 nm, and the overall thickness of the absorbing multilayer structure being between 5 and 1000 nm, and wherein the layers of a dielectric nature of the solar selective absorbing coating are deposited by means of reactive sputtering including inert gas and reactant gas in the chamber or part of the chamber where these dielectric layers are deposited, while the metallic layers of the solar selective absorbing coating are deposited by DC sputtering, introducing inert gas exclusively in the chamber or part of the chamber where these metallic layers are deposited; #10#
wherein:
the absorbing multilayer structure has a homogeneous area with dielectric layers of equal composition and thickness, and metal layers of equal composition and thickness;
the absorbing multilayer structure has two or more homogeneous areas so that the dielectric layers differ in material and/or thickness from one area to another, and the metal layers differ in material and/or thickness from one area to the other area;
the substrate includes stainless steel;
the reflecting metallic layer includes molybdenum (Mo);
the first homogeneous area of the multilayer structure includes alternating layers of silicon and aluminium oxide (SiAlOx) and Mo;
the second homogeneous area of the multilayer structure includes alternating layers of SiAlOxand Mo; and
the anti-reflecting dielectric layer includes SiAlOx.
4. The solar selective absorbing coating of
5. The solar selective absorbing coating of
6. The solar selective absorbing coating of
7. The solar selective absorbing coating of
8. The solar selective absorbing coating of
9. The solar selective absorbing coating of
10. The solar selective absorbing coating of
11. The solar selective absorbing coating of
12. The solar selective absorbing coating of
13. The solar selective absorbing coating of
14. The solar selective absorbing coating of
15. The solar selective absorbing coating of
16. The solar selective absorbing coating of
17. The solar selective absorbing coating according to
18. The solar selective absorbing coating of
19. The solar selective absorbing coating of
20. The solar selective absorbing coating of
21. The solar selective absorbing coating according to
22. The solar selective absorbing coating according to
|
|||||||||||||||||||||||||||||||||
The present invention refers to a selective absorbing coating that comprises of: (i) a substrate, one or more metallic layers that confer low emissivity properties (ii) a structure of multiple alternating subnanometer thickness dielectric and metallic layers in which solar energy absorption is produced; and (iii) a layer or multilayered structure that provides antireflective properties.
The invention also includes the method and process of manufacture and the use of said selective solar absorbent coating.
The capture of solar energy, in terms of the thermal capture aspect, is of increasing technological and economic importance from the point of view of hot water production, heating and refrigeration at a domestic level as well as electricity generation in solar thermoelectric power plants.
These systems require maximum solar energy absorption and the minimum possible loss of energy. With this end in mind, these systems are configured in vacuum tubes or similar structures that reduce losses by conduction and convection and possess coatings with a great capacity for solar energy absorption and low emissivity characteristics to reduce energy losses through thermal radiation in far infrared.
Consequently, in the domestic area as well as in the production of electricity, selective absorbent coatings play an essential role. There are numerous records of absorbent coatings such as those described in patents WO2005/121389, U.S. Pat. Nos. 4,582,764, 4,628,905, 5,523,132, US2004/0126594, US2005/0189525, US2007/0209658, WO97/00335, as well as several others. In all of these the absorbent coating consists of a metallic layer that provides low emissivity characteristics, one or more layers of dielectric materials doped with “Cermets” metallic elements, which act as absorbent layers for solar radiation and a dielectric layer that provides anti-reflective properties. In some of these there is also an additional dielectric layer that acts as a blocking layer against the diffusion of different materials. The layers of cermets are absorbent layers, complex refraction index, where the capacity for absorption is provided by the co-dopant metal element whose concentration can be constant or gradual within each of the layers.
Cermets are habitually oxides or metal nitrides doped with metallic elements such as Mo, Ni, Ti, Ta, Al, etc., that are usually deposited through codeposition techniques through reactive cathodic spraying “reactive sputtering”. Codeposition through reactive sputtering consists in simultaneous evaporation of two materials through sputtering in the presence of, in addition to the inert gas, a reactive Gas, oxygen, nitrogen etc., residual in the deposition chamber. The residual gas reacts with one of the evaporated materials forming the corresponding dielectric compound, while part of the other compound is deposited in metal form. Reactive gas reacts both with the material that forms the dielectric compound and the doping metal, so to obtain the cermets with the appropriate absorption a stringent control of the stoichiometry process is required. The stoichiometry process is conditioned by the composition and partial pressures of the gases in the vacuum chamber in relation to the reactive gas consumption, and therefore depends on the evaporation speed, that is, cathode power, of its state, making accurate control of the stoichiometry process very difficult, requiring certain feedback mechanisms that can negatively affect the properties of the coatings.
Likewise, part of the codopant metal also reacts with the reactive gas and forms dielectric compounds, so this metal does not therefore contribute to the absorption of the layer and requires large concentrations of codopant metal. Besides, this technique also presents limitations when choosing codopant metals as they should possess much less affinity for the reactive gas than the principal metal that forms the dielectric compound.
This invention seeks to resolve all the difficulties set out above, as each of the cermet layers are replaced by an alternating multilayered dielectric and metal structure, with very thin layers, less than 10 nm and mainly under 1 nm. Dielectric layers are deposited through reactive sputtering, including inert gas and reactive gas in the chamber or part of the chamber where dielectric coatings are deposited. Metal layers are deposited through DC sputtering, introducing inert gas exclusively in the chamber or part of the chamber where metallic layers are deposited. As a result, precise control of the stoichiometry process is not required, since the depositing of the dielectric layers requires a composition of gases that guarantees the total reaction of the evaporated metal, while the metal nature of the alternating layers is determined by the inert gas introduced as process gas. As the depositing of both types of materials is realized in different chambers or in isolated parts of the same deposition chamber, gas mixture is minimal and no chemical reaction of the constituent material of the metal layers is produced. Likewise, as the deposition of dielectric and metal layers is realized in different places and with different gas compositions, there is no limit to the composition of dielectric and metallic layers, which can even be taken from the same batch of metal, forming dielectric layers from a metal element, such as oxides or nitrides of a metal, and metal layers of the same element.
The selective solar coating in this invention is designed to absorb solar energy and transform it into heat with low emissivity properties, facilitating and making the manufacturing process more robust and reliable and allowing greater possibilities for its design and optimisation. The coating deposited on the substrate, which can be metallic or dielectric, ensures the mechanical and thermal stability of the coating, and is essentially characterised by including:
Metal elements such as steel, stainless steel, copper or aluminium, and non-metallic elements such as glass, quartz or ceramic materials or polymers are included in this invention as substrate materials. The substrate can be subject to treatments, such as the oxidation of the superficial layer or thermal and cleaning treatments that optimise adhesion of the coating and therefore its mechanical and environmental stability.
Likewise, the current invention includes a coating absorbent of solar energy and reflective in medium-far infrared, that contains one or more metal layers on the substrate, highly reflective in medium-far infrared, a multilayered structure with thin alternating metallic-dielectric layers and one or more dielectric layers that form the antireflective structure for solar energy. The coating, according to the invention, is unique because of the highly reflective metal layer or layers deposited on the substrate include a metallic material selected from the group formed by silver (Ag), gold (Au), aluminium (Al), chromium (Cr), molybdenum (Mo), copper (Cu), nickel (NI), titanium (Ti), niobium (Nb), tantalum (Ta), tungsten (W), palladium (Pd) or an alloy of the same or mixtures of the same.
According to another characteristic of the invention, the layers of dielectric material in the absorbent multi-layer structure consist in metal oxides and/or metal nitride elements, with a refraction index of between 1.4 and 2.4. The coating, according to the invention, is distinguished because the metal oxides are selected from the group consisting of tin oxides, zinc oxides, aluminium oxides, titanium oxides, silicon dioxides, nickel oxides, chromium oxides, indium oxides or a mixture of the same. Correspondingly, the coating, according to the invention, is unique because the nitrides of metal elements are selected from the group formed by silicon nitrides, chromium nitrides and aluminium nitrides, or mixtures of the same.
Likewise, the coating, according to the invention, is unique because the metal layers that form part of the absorbent multilayered structure are made from a metal selected from the group formed by silver (Ag), gold (Au), aluminium (Al), chromium (Cr), molybdenum (Mo), copper (Cu) nickel (Ni), titanium (Ti), niobium (Nb), tantalum (Ta), tungsten (W), palladium (Pd) or any alloy of the same or mixture of the same.
The invention equally contemplates the presence of one, or more dielectric layers that act as an antireflective structure and these are made from metal oxides and/or metal nitride elements, with a refraction index between 1.4 and 2.4. The coating, according to the invention, is unique because metal oxides are selected from the group formed by tin oxides, zinc oxides, aluminium oxides, titanium oxides, silicon dioxides, nickel oxides, chromium oxides, indium oxides or mixtures of the same. Correspondingly, the coating, according to the invention, is unique because the nitrides of metal elements are selected the group formed by silicon nitrides, chromium nitrates and aluminium nitrides, or mixtures of the same.
In the context of the current invention the term “metallic alloy” means any of those that these metals can form between them or with other metals.
According to another characteristic of the invention, the thickness of each of the reflecting metallic layers in medium-far infrared, and each of the layers of dielectric material of the antireflective structure is between 1 and 500 nm. In addition, according to another characteristic of the invention, the thickness of each of the metallic and dielectric layers of the absorbing multilayered structured is less than 10 nm, with a total number of layers of the multilayered structure of more than 20. The multilayered structure can be configured as a homogenous zone, in which all the dielectric layers are of the same material and have the same thickness and all the metal layers are of the same metal and thickness, in various differentiated zones, in which each zones is configured as a homogenous zone and differs from the other zones in the material used for the dielectric layers and/or the metal used for the metal layers and/or the thickness of each of the metallic or dielectric layers, or can be configured as a gradual zone where the thickness of the metal and/or dielectric layers vary gradually. The preference is for the multilayered structure to be configured with at least two differentiated zones, in which the composition and/or thickness of the layers of one of the areas is different to the composition and/or thickness of the other.
All in all, the total number of layers of coating is over 25 and the total thickness is between 100 nm and 2000 nm.
The purpose of the invention is the fact that the different layers of coating are deposited through physical deposition techniques in vacuum in vapour phase (PVD, physical vapour deposition) such as thermal evaporation, electron gun, ionic implantation or “sputtering”, by chemical deposition in vapour phase (CVD, chemical vapour deposition) or through electrolytic baths, with the sputtering technique being the preferred method for this task.
Another purpose of this invention is the use of the coating in absorbent tubes for parabolic cylinder collectors in solar thermoelectric plants.
Another purpose of this invention is the use of the coating in solar panels for hot water, heating or household refrigeration, both in the form of absorbent tubes as well as absorbent plates.
This invention also has the benefit that the coating can be used in capture systems at solar tower-type thermoelectric power plants, in which solar energy reflected by a multitude of heliostats is concentrated in the capture system positioned in a tower.
And, finally, it is also the purpose of this invention to use the coating in the capture system of stirling dish systems.
With the aim of illustrating the advantages and properties of the coating in this invention and with the object of better understanding the characteristics of the invention, a detailed description of the ideal scenario will be provided, based on a set of drawings enclosed with this specification, where the following, for illustration but not limiting purposes, are represented:
In the above figures the numerical references correspond to the following parts and elements.
The selective solar radiation absorbing coating in the invention includes, as shown in
The substrate (1) can be a metallic or dielectric material or a combination of both, that ensures mechanical stability of the coating.
The metallic reflecting layer (2) consists, in turn, of at least one highly reflective layer in medium-far infrared (2.5-20 μm wave length), said metallic layer being deposited on the substrate itself.
The absorbent multilayered structure (3) consists, in turn, in a series of alternating dielectric (5) and metallic (6) layers, deposited on the reflecting metallic layer (2), and can be of the same or different thickness and/or composition:
The antireflective structure (4) consists in at least one dielectric layer that provides solar energy antireflective properties.
The substrates (1) correspond to metals such as steel, stainless steel, copper and aluminium and dielectrics such as glass, quartz, polymeric materials or ceramic materials, or a combination of different materials.
For the reflective metal layer (2) silver (Ag), gold (Au), aluminium (Al), chromium (Cr), Molybdenum (Mo), Copper (Cu), nickel (Ni), titanium (Ti), niobium (Nb), tantalum (Ta), tungsten (W), palladium (Pd) or a mixture of two or more of these or an alloy of said metals are used. These metal layers (2) have a thickness of between 5 and 1000 nm.
The layers of dielectric material (5) of the different configurations of absorbent multi-layered structures have a refraction index of between 1.4 and 2.4. For this purpose metal oxides and/or metal element nitrides, such as tin oxides zinc oxides, aluminium oxides, titanium oxides, silicon dioxides, silicon-aluminium, nickel oxides, chromium oxides, niobium oxides, tantalum oxides or mixtures of the same are used; as well as silicon nitrides, chromium nitrides and aluminium nitrides, or mixtures of the same. The thickness of the dielectric layers (5) is less than 10 nm, preferably below 1 nm, the number of dielectric layers is more that 10, and the total thickness of the dielectric layers of the absorbent layer structure (3) is between 5 and 1000 nm.
For the realisation of the metal layers (6) of the different configurations of the absorbent multilayer structures silver (Ag), gold (Au) aluminium (Al), chromium (Cr), Molybdenum (Mo), copper (Cu), nickel (Ni), titanium (Ti), niobium (Nb), tantalum (Ta), Tungsten (W) palladium (Pd), or an alloy of the same or mixtures of the same are used. The thickness of the metal layers (6) are less than 10 nm, preferably below 1 nm, the number of metal layers is above 10, and the total thickness of the metal layers of the absorbent multilayered structure (3) is between 5 and 1000 nm.
The layers that form the antireflective structure (4) have a refraction index of between 1.4 and 2.4. For this purpose, metal oxides and/or nitrides of metal elements are used, such as tin oxide, zinc oxide, aluminium oxide, titanium oxides, silicon oxides, silicon-aluminium oxides, nickel oxides, or mixtures of the same; as well as silicon nitrides and aluminium nitrides, or mixtures of the same. The thickness of the layers of dielectric material of the antireflective structure is between 5 and 1000 nm.
Finally, with the idea of increasing adherence between the coating and the substrate, the substrate can be subjected to diverse treatments, such as the oxidation of the superficial layer or thermal and cleaning treatments, since improving the adhesion of the coating implies more mechanical and environmental stability.
So to obtain the coating of the invention in a manner that a first metal layer is placed (2) onto the substrate (1) of the metal or dielectric material, and onto this is placed the first metal layer (2), and onto this is deposited the first of the layers that form the absorbent multilayered structure, with the first layer being either the dielectric (5) or metal (6) material. After this first layer the rest of the metal (6) and dielectric (5) layers are alternately deposited, and can have identical or different thicknesses and/or compositions, forming the absorbent multilayered structure. After the last of the layers of the absorbent multilayered structure, the different layers that form the antireflective structure are added.
For the successive addition of the different layers (2, 4, 5, 6 . . . ) to the transparent (1) substrate, a metal and/or dielectric compound deposition procedure is used, such as chemical vapour deposition (CVD) or physical vapour deposition (PVD). The preferred manner, within the range of PVD techniques, is “magnetron sputtering”.
To determine solar absorbance and thermal emissivity, an spectroscopic study of the coating is carried out, studying the reflectance in the spectral visible-Infrared range, together with the solar energy spectrum and thermal emission spectrum at 400° C., giving low reflectance values in the solar spectrum zone, which means high absorbance (above or equal to 95%), and high reflectance values in the thermal emission zone, which mean low emissivity (less than or equal to 0.2).
Evidently, variants of the described procedure exist, known by experts in the field, which depend on which materials are used and the use of the coatings obtained.
The selective solar absorbent coating of the invention can be used as a coating for laminar materials or tubes selected from the group formed by steel, stainless steel, copper, aluminium or ceramic materials, in the absorbent elements of tower-type solar thermoelectric power plants and for use in absorbent element in stirling dish systems or for use in absorbent tubes of solar thermoelectric power plants with parabolic-cylinder collectors.
Some examples of coatings according to the invention are shown below, as well as their reflectance properties and absorbance at different wave lengths. Said examples allow for the visualisation of the coating's properties.
On a substrate (1) of stainless steel 304 a layer of Mo of 300 nm is deposited. On this layer of Mo the absorbent multilayer structure consisting in two differentiated zones is deposited. The first zone has a total thickness of 52 nm, and consists in 285 layers of SiAIOx with a thickness of 0.08 nm alternated with another 285 of Mo with a thickness of 0.1 nm. The second zone has a total thickness of 57 nm, and consists in 390 layers of SiAIOx with a thickness of 0.08 nm alternated with another 390 of Mo with a thickness of 0.06 nm. The thickness of each of these layers is understood to mean the average thickness obtained from the data provided by a quartz crystal microbalance. On the absorbent multilayer structure an antireflective reflective layer of SiAIOx with a thickness or 87 nm has been deposited.
With the aim of determining solar absorbance and thermal emissivity, a spectroscopic study of the coating in example 1. was performed and
On a substrate (1) or stainless steel 304 a layer of Ni of 110 nm is deposited. On this layer of Ni the absorbent multilayer structure consisting in two differentiated zones is deposited. The first zone has a total thickness of 78 nm and consists in 340 layers of SiAIOx with a thickness of 0.085 nm alternated with another 340 of Ni with a thickness of 0.145 nm. The second zone has a total thickness of 55 nm, and consists in 490 layers of SiAIOx with a thickness of 0.08 nm alternated with another 490 of Ni with a thickness of 0.03 nm. The thickness of each of these layers is understood to mean the average thickness obtained from the data provided by a crystal quartz microbalance. On the absorbent multi-layer structure is placed an antireflective layer of SiAIOx with a thickness of 67 nm.
With the aim of determining solar absorbance and thermal emissivity, a spectroscope study of the coating of example 2 was performed and
Alonso Esteban, Rafael, Subias Domingo, Jesus Mario, Villuendas Yuste, Francisco, Heras Vila, Carlos, Martinez Sanz, Noelia, Alcañiz Garcia, Carlos, Pelayo Zueco, Javier
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 3272986, | |||
| 4101200, | Mar 07 1975 | Balzers Patent-und Beteiligungs-Aktiengesellschaft | Coating composition for a light transmitting absorbing coating on substrates |
| 4282290, | Jan 23 1980 | The United States of America as represented by the Secretary of the Air | High absorption coating |
| 4437455, | May 03 1982 | Engelhard Corporation | Stabilization of solar films against hi temperature deactivation |
| 4582764, | Sep 24 1982 | Energy Conversion Devices, Inc. | Selective absorber amorphous alloys and devices |
| 4628905, | Oct 08 1982 | University of Sydney | Solar selective surface coating |
| 5523132, | Jul 19 1991 | The University of Sydney | Thin film solar selective surface coating |
| 20020012797, | |||
| 20020073988, | |||
| 20040126594, | |||
| 20050134959, | |||
| 20050189525, | |||
| 20050280890, | |||
| 20070209658, | |||
| 20100313875, | |||
| CN1159553, | |||
| EP27718, | |||
| EP104708, | |||
| EP107412, | |||
| ES2232557, | |||
| JP2006500624, | |||
| JP222863, | |||
| WO2005121389, | |||
| WO9700035, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Oct 08 2009 | Abengoa Solar New Technologies, S.A. | (assignment on the face of the patent) | / |
| Date | Maintenance Fee Events |
| Date | Maintenance Schedule |
| Mar 29 2019 | 4 years fee payment window open |
| Sep 29 2019 | 6 months grace period start (w surcharge) |
| Mar 29 2020 | patent expiry (for year 4) |
| Mar 29 2022 | 2 years to revive unintentionally abandoned end. (for year 4) |
| Mar 29 2023 | 8 years fee payment window open |
| Sep 29 2023 | 6 months grace period start (w surcharge) |
| Mar 29 2024 | patent expiry (for year 8) |
| Mar 29 2026 | 2 years to revive unintentionally abandoned end. (for year 8) |
| Mar 29 2027 | 12 years fee payment window open |
| Sep 29 2027 | 6 months grace period start (w surcharge) |
| Mar 29 2028 | patent expiry (for year 12) |
| Mar 29 2030 | 2 years to revive unintentionally abandoned end. (for year 12) |