WO2018171731A1 - 平面加热结构 - Google Patents
平面加热结构 Download PDFInfo
- Publication number
- WO2018171731A1 WO2018171731A1 PCT/CN2018/080257 CN2018080257W WO2018171731A1 WO 2018171731 A1 WO2018171731 A1 WO 2018171731A1 CN 2018080257 W CN2018080257 W CN 2018080257W WO 2018171731 A1 WO2018171731 A1 WO 2018171731A1
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- WO
- WIPO (PCT)
- Prior art keywords
- planar heating
- heating structure
- layer
- transparent conductive
- nano
- Prior art date
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Images
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/84—Heating arrangements specially adapted for transparent or reflecting areas, e.g. for demisting or de-icing windows, mirrors or vehicle windshields
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60J—WINDOWS, WINDSCREENS, NON-FIXED ROOFS, DOORS, OR SIMILAR DEVICES FOR VEHICLES; REMOVABLE EXTERNAL PROTECTIVE COVERINGS SPECIALLY ADAPTED FOR VEHICLES
- B60J1/00—Windows; Windscreens; Accessories therefor
- B60J1/002—Windows; Windscreens; Accessories therefor with means for clear vision, e.g. anti-frost or defog panes, rain shields
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/84—Heating arrangements specially adapted for transparent or reflecting areas, e.g. for demisting or de-icing windows, mirrors or vehicle windshields
- H05B3/86—Heating arrangements specially adapted for transparent or reflecting areas, e.g. for demisting or de-icing windows, mirrors or vehicle windshields the heating conductors being embedded in the transparent or reflecting material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60S—SERVICING, CLEANING, REPAIRING, SUPPORTING, LIFTING, OR MANOEUVRING OF VEHICLES, NOT OTHERWISE PROVIDED FOR
- B60S1/00—Cleaning of vehicles
- B60S1/02—Cleaning windscreens, windows or optical devices
- B60S1/023—Cleaning windscreens, windows or optical devices including defroster or demisting means
- B60S1/026—Cleaning windscreens, windows or optical devices including defroster or demisting means using electrical means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60S—SERVICING, CLEANING, REPAIRING, SUPPORTING, LIFTING, OR MANOEUVRING OF VEHICLES, NOT OTHERWISE PROVIDED FOR
- B60S1/00—Cleaning of vehicles
- B60S1/02—Cleaning windscreens, windows or optical devices
- B60S1/56—Cleaning windscreens, windows or optical devices specially adapted for cleaning other parts or devices than front windows or windscreens
- B60S1/58—Cleaning windscreens, windows or optical devices specially adapted for cleaning other parts or devices than front windows or windscreens for rear windows
- B60S1/586—Cleaning windscreens, windows or optical devices specially adapted for cleaning other parts or devices than front windows or windscreens for rear windows including defroster or demisting means
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/02—Details
- H05B3/06—Heater elements structurally combined with coupling elements or holders
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/20—Heating elements having extended surface area substantially in a two-dimensional plane, e.g. plate-heater
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/84—Heating arrangements specially adapted for transparent or reflecting areas, e.g. for demisting or de-icing windows, mirrors or vehicle windshields
- H05B3/845—Heating arrangements specially adapted for transparent or reflecting areas, e.g. for demisting or de-icing windows, mirrors or vehicle windshields specially adapted for reflecting surfaces, e.g. bathroom - or rearview mirrors
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B2203/00—Aspects relating to Ohmic resistive heating covered by group H05B3/00
- H05B2203/013—Heaters using resistive films or coatings
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B2214/00—Aspects relating to resistive heating, induction heating and heating using microwaves, covered by groups H05B3/00, H05B6/00
- H05B2214/04—Heating means manufactured by using nanotechnology
Definitions
- the present invention relates to a planar heating structure, and more particularly to a planar heating structure having high light transmittance and uniform heating.
- the automotive industry faces various problems caused by the natural climate.
- One of them is the condensation of water and gas generated by the temperature difference between the inside and outside of the car.
- the moisture that condenses on the front and rear gear glass of the car causes the so-called window fogging phenomenon, which obviously and seriously reduces the visibility of the front and rear gear glasses, so that the driver's viewing angle and visibility are seriously reduced.
- the combination of the metal wire and the surface of the glass is not easy, and a defect that cannot be completely attached often occurs, or a part of the film is attached and the other part is detached, so that the problem of uneven heating occurs in the glass attached to the same line body, and the influence is affected.
- the fog/frost effect or severe damage causes the glass to break.
- the metal wires are not transparent, only the rear window glass can utilize such technology, and the front and side glass cannot be used for defogging.
- the line width of the wire needs to be controlled, and the line spacing must be maintained at a considerable distance, so that the temperature difference of the heating unevenness is easily generated on the same window glass according to the distance from the metal wire.
- some of the defogging/frost is caused, and some of the excess dead spots of fog/frost remain.
- the heating wire after the breakpoint will not be used due to the lack of energy supply.
- the reliability of the class technology is not high and it is prone to abnormalities. When an abnormality occurs, the heating wire is buried between the two layers of glass and sticks to death, so that the only way to repair is to replace the entire window glass, the cost is too high, and the penetration rate is seriously affected.
- the present invention provides a planar heating structure that uniformly heats the target and has good visibility and can rapidly increase the temperature to a default temperature compared to the prior art.
- the invention provides a planar heating structure comprising a glass substrate layer, a nano metal transparent conductive layer and a first protective layer.
- a nano-metal transparent conductive layer is disposed on the glass substrate layer and receives a voltage to generate thermal energy.
- a first protective layer is disposed on the nano-metal transparent conductive layer and completely covers the nano-metal transparent conductive layer.
- the invention provides a planar heating structure bonded to glass, comprising a flexible substrate layer, a nano metal transparent conductive layer, an adhesive layer and a release film.
- the nano-metal transparent conductive layer is disposed on the flexible substrate layer and receives a voltage to generate thermal energy.
- the adhesive layer is disposed on the nano metal transparent conductive layer.
- the release film is formed on a surface of the adhesive layer away from the nano-metal transparent conductive layer.
- the planar heating structure further includes a second protective layer disposed between the glass substrate layer or the flexible substrate layer and the nano metal transparent conductive layer.
- the second protective layer is an optical functional layer.
- the optically functional layer is any one or combination of an anti-reflective layer, an anti-UV layer.
- the substrate layer is made of a transparent glass or a flexible transparent film.
- the nano-metal transparent conductive layer is made of nano-silver.
- FIG. 1 is a schematic structural view of a planar heating structure 1 according to a preferred embodiment of the present invention.
- 2A is a histogram of the length of a purified metal nanowire in accordance with an embodiment of the present invention.
- 2B is a schematic diagram of heating elevated temperature versus time in an embodiment of the invention.
- FIG. 3 is a schematic structural view of another embodiment of a planar heating structure 1 based on FIG.
- FIG. 4 is a schematic structural view of another planar heating structure 2 according to the present invention.
- FIG. 5A is a schematic structural view of another planar heating structure 3 according to the present invention.
- Figure 5B shows the structure of another embodiment of the planar heating structure 3 based on the disclosure of Figure 5A.
- FIG. 6 is a schematic structural view of a planar heating structure 4 according to the present invention.
- FIG. 7 is a schematic view showing the combination of a heating structure and a window glass according to another embodiment of the present invention.
- planar heating structure of the present invention are described below by way of specific specific examples, and those skilled in the art can readily appreciate other advantages and effects of the present disclosure from the disclosure of the present specification.
- the present invention may also be implemented or applied by other specific examples.
- the details of the present specification may also be based on different viewpoints and applications, and various modifications and changes may be made without departing from the spirit of the present invention.
- the illustrations of this creation are only for a brief description, and are not depicted in terms of actual size, thickness, and scale, that is, the actual dimensions of the relevant composition are not reflected, which will be described first.
- FIG. 1 is a schematic view of a planar heating structure 1 according to a preferred embodiment of the present invention.
- the planar heating structure 1 can be used to heat various transparent substrates to achieve a defogging/defrosting effect.
- it can be applied to the front and rear gear glass, the car side glass and the rear view mirror of the automobile, or to the glass refrigerator for business use, or to heat the fish tank.
- the planar heating structure 1 includes a glass substrate layer 11, a transparent conductive layer 12, and a first protective layer 13.
- the glass substrate layer 11 is a substrate constituting a transparent portion of the window, and may be any material having appropriate transparency and sufficient strength to pass safety regulations of automobiles. For example, but not limited to, high-strength heat-resistant glass or plastic, it is not limited. It can also be a composite structure of glass and plastic.
- the transparent conductive layer 12 is disposed on the glass substrate layer and receives electric energy to raise the temperature of the planar heating structure 1. For example, after receiving a voltage, the transparent conductive layer 12 generates a high potential to a low potential. The current flowing. Since no active circuit exists in the transparent conductive layer 12, the electrical energy consumes energy by raising the temperature of the transparent conductive layer 12 to achieve balance. This elevated thermal energy is evenly conducted to the glass substrate layer 11, whereby the present invention achieves the effect of heating the glass substrate layer 11, so that the glass substrate layer 11 as a window can achieve the purpose of defogging.
- the transparent conductive layer 12 is composed of a nano metal material.
- the nano metal material can be a nano silver material, has better metal characteristics, and at the same time maintains sufficient transparency, so that the invention can realize the purpose of window defogging. At the same time, to ensure that the light transmittance of the window is in line with national automotive standards.
- “nanometal material” as used herein refers to a metal wire comprising an elemental metal, a metal alloy, or a metal compound, including a metal oxide.
- the metal nanowires have at least one cross-sectional dimension of less than 500 nm, and preferably less than 100 nm, and more preferably less than 50 nm.
- the width or equivalent diameter of the nanostructures is in the range of 10 nm to 40 nm, 20 nm to 40 nm, 5 nm to 20 nm, 10 nm to 30 nm, 40 nm to 60 nm, or 50 nm to 70 nm.
- the metal nanowires have an aspect ratio (length: width) of more than 10, preferably more than 50, and more preferably more than 100. Nanowires with suitable performance typically have an aspect ratio in the range of 10 to 100,000.
- a larger aspect ratio facilitates obtaining a transparent conductor layer because this property allows the transparent conductive layer 12 to form a more efficient conductive network while allowing the overall density of the conductive nanowires to be reduced to achieve high transparency.
- the density of the nanowires that reach the conductive network does not have to be too high to achieve a set transmittance so that the conductive network is substantially transparent.
- Metal nanowires can be dominated by any metal, including but not limited to silver, gold, copper, nickel, and gold-plated silver.
- the length/diameter of the metal nanowires is also related to whether the conductive properties of the transparent conductive layer are excellent.
- the length of the nanowire structure is in the range of 5 ⁇ m to 30 ⁇ m, or between 15 ⁇ m and 50 ⁇ m, 25 ⁇ m to 75 ⁇ m, It is in the range of 30 ⁇ m to 60 ⁇ m, 40 ⁇ m to 80 ⁇ m or 50 ⁇ m to 100 ⁇ m.
- 2A is a histogram of the length of the purified metal nanowire according to an embodiment of the present invention.
- the metal nanowire having a length of less than 25 ⁇ m is greater than 80%, and the metal nanometer is longer than 8 ⁇ m.
- the proportion of the wire is also greater than 75%, and the proportion of the metal nanowires longer than 5 ⁇ m is also greater than 92%.
- Other various possible combinations have also been disclosed in the drawings, please refer to the drawings, and details are not described herein again.
- transparent conductive layer refers to a metal nanowire network layer that provides a conductive medium of a transparent conductor.
- the combination of the network layer of metal nanowires and the substrate is also referred to as a "transparent conductive layer.” Since conductivity is achieved by the infiltration of charge from one metal nanowire to another metal nanowire, sufficient metal nanowires must be present in the conductive layer to reach the electroosmotic threshold and become conductive.
- the surface conductivity of the conductive layer is inversely proportional to its surface resistivity, which is sometimes referred to as sheet resistance, which can be measured by methods known in the art.
- the substrate layer is a part of the transparent conductive layer and is disposed on the glass substrate layer.
- the mechanical and optical properties of the substrate may be altered or compromised by the high loading of any of the particles therein.
- the aspect ratio of the metal nanowires is sufficiently high, the matrix of the silver nanowires will be allowed to form a conductive network with a threshold loading level of about 35% by weight. This loading level does not affect the mechanical or optical properties of the substrate.
- the metal nanowires can limit the horizontal load above the load level without adversely affecting the mechanical or optical properties of the substrate.
- the silver nanowires can typically be less than about 60% by weight load, more typically less than about 40% by weight, and more typically less than about 20% by weight, and even more typically less than about 10% by weight. This value depends entirely on the size and spatial dispersion of the nanowires.
- a transparent conductor of adjustable conductivity (or surface resistivity) and light transmittance can be provided by adjusting the loading level of the metal nanowires.
- the mechanical and optical properties of the substrate may be altered or impaired by the high loading of any of the particles therein.
- the high aspect ratio of the metal nanowires may, for silver nanowires, preferably from about 0.05 ⁇ g/cm 2 to about 10 ⁇ g/cm 2 , more preferably from about 0.1 ⁇ g/cm 2 to about 5 ⁇ g/cm 2 and more preferably about 0.8.
- a conductive network through the substrate is formed at a threshold surface loading level of from ⁇ g/cm2 to about 3 ⁇ g/cm2. These surface loading levels do not affect the mechanical or optical properties of the substrate.
- the numerical values disclosed above strongly depend on the size and spatial dispersion of the nanowires.
- a transparent conductor having an adjustable electrical conductivity (or surface resistivity) and light transmittance can be provided by adjusting the loading level of the metal nanowires.
- the substrate is from about 10 nm to 5 ⁇ m thick, from about 20 nm to 1 ⁇ m thick, or from about 50 nm to 200 nm thick.
- the matrix has a refractive index of from about 1.3 to 2.5 or from about 1.35 to 1.8.
- the optical transparency or sharpness of the transparent conductor can generally be quantitatively defined by parameters including light transmission and haze.
- Light transmittance refers to the percentage of incident light that is transmitted through the medium.
- the transparent conductor has a light transmission of at least 50%, at least 60%, at least 70%, or at least 80% and can be as high as at least 91% to 92%.
- the haze is the light diffusion index. It refers to the percentage of light that is separated from the incident light and scattered during transmission. Unlike light transmission, which is primarily a property of the medium, haze is often product-dependent and is typically caused by surface roughness and particle or compositional inhomogeneities embedded in the medium. In various embodiments, the haze of the transparent conductor is no greater than 10%, no greater than 8%, or no greater than 5%, and can be as low as no greater than 2% to 0.5%.
- the optical properties of the bare silver nanowire film on the PET are greater than 80%.
- the planar heating structure 1 can achieve a condition that the transmittance is greater than 85 percent and the haze is less than 3 percent.
- the transparent conductive layer 12 is The resistance of square centimeters is less than or equal to ten ohms.
- the anti-UV protective agent With regard to the anti-UV protective agent, light-sensitive substances easily absorb light and undergo or cause complicated photochemical activities.
- One type of photochemical activity involves exciting a compound from a ground state to a higher energy level (ie, an excited state). The excited state is transient and will typically decay back to the ground state and release heat. However, the transient excited state can also cause a complex cascade reaction with other substances. Regardless of the failure mechanism, it was found that some photochemical activities caused corrosion of silver nanostructures via oxidation: Ag0 ⁇ Ag++e-
- the corrosion is inhibited by suppressing the photochemical activity of the excited state or helping to quickly return to the ground state.
- one or more light stabilizers into an optical stack (eg, incorporating one or more layers, particularly one or more layers adjacent to the silver nanostructures), repression may result in Silver photochemical activity of corrosion.
- the UV resistant layer comprises one or more UV resistant materials that absorb photons in the UV region (typically defined as light below 390 nm), thereby blocking or significantly attenuating UV in the incident light that would otherwise enter the optical stack and degrade the silver nanostructures Light.
- the UV resistant material is typically a compound having an unsaturated chemical bond.
- an electronically excited state is produced when a UV blocking material absorbs photons. The excited state is returned to the ground state by energy transfer or electron transfer, thus dissipating photon energy.
- the UV resistant layer can be any of the substrates described herein coated with a thin layer of UV resistant material.
- the UV resistant layer can be in the main portion of the layer with one or more UV resistant materials.
- the UV resistant layer may suitably serve as an OCA (Optical Clear Adhesive, OCA) layer.
- OCA Optical Clear Adhesive
- the UV-resistant OCA layer serves both as a dual purpose for blocking UV light and bonding the two sub-portions of the optical stack.
- the anti-UV protectant constituting the anti-UV layer may be any of the following types of compounds: in general, it is non-volatile (having a boiling point of at least 150 ° C) and may be liquid or solid. It may be an organic small molecule having a molecular weight of not more than 500, or an oligomer having 2 to 100 monomers or a polymer of more than 100 monomers.
- An olefin having at least one carbon-carbon double bond having at least one carbon-carbon double bond. Double bonds make olefins a candidate for sacrificial oxidation reactions.
- the olefin may have a linear, cyclic carbon skeleton or a combination of a linear and a cyclic carbon skeleton.
- the olefin may be further substituted on the carbon skeleton by a hydroxyl group, an alkoxy group, a thiol group, a halogen group, a phenyl group or an amine group.
- suitable olefins have alternating double bonds and single bond configurations to provide an extended conjugated structure. This conjugated structure allows the group to be delocalized to stabilize it.
- conjugated olefins include, but are not limited to, carotenes or carotenoids, certain anthraquinones or terpenoids.
- the olefin can have multiple but non-conjugated double bonds.
- non-conjugated olefins include certain oximes, rosins, polybutadienes, and the like.
- certain olefins are also tackifiers and can be incorporated directly into OCA.
- Tantalum is a subgroup of olefins. It is derived from a variety of plants, especially resins made from conifers. Although hydrazine contains a wide variety of hydrocarbons, it all contains at least one isoprene unit. The ruthenium may have a cyclic and a non-cyclic carbon skeleton. As used herein, hydrazine also includes anthraquinone, which is a derivative of hydrazine or oxidized or rearranged via a carbon skeleton.
- the light stabilizer is ruthenium. ⁇ A cyclic oxime containing two isoprene units. The ring double bond is easily subjected to an oxidation reaction to form an epoxide.
- Certain metals can be used as inorganic light stabilizers because they can sensitize photochemical activities. Examples include phosphonium salts and zinc or cadmium salts. The entire disclosures of all of these patents are hereby incorporated by reference.
- the antioxidant is particularly effective in suppressing corrosion caused by oxygen.
- the antioxidant acts as a capture agent to remove oxygen by reacting directly with molecular oxygen.
- the antioxidant can also act to remove the groups formed in the initial oxidation reaction, thereby preventing the chain reaction initiated by the other groups.
- a particularly preferred antioxidant is ascorbate, which may be an ascorbate salt (such as sodium ascorbate or potassium ascorbate) or ascorbic acid.
- antioxidants may include mercaptans, hydrazines, and sulfites (e.g., sodium sulfite and potassium sulfite).
- a light stabilizer or a combination of any of the light stabilizers described herein can be incorporated into any of the layers of the given optical stack.
- the light stabilizer can be combined with the coating solution prior to coating.
- the light stabilizer can be incorporated into the nanostructure layer, overcoat, undercoat, substrate, or adhesive layer (eg, OCA) via co-deposition.
- the method of disposing the transparent conductive layer 12 can be applied to one surface of the substrate layer 11 by a coating method, and the coating method can be, for example, spin coating, dipping, pouring, dripping, spraying, spraying fine mist ( Coating, knife coating, brushing or printing, such as inkjet printing, screen printing, gravure printing, lithography or mobile printing.
- a coating method can be, for example, spin coating, dipping, pouring, dripping, spraying, spraying fine mist ( Coating, knife coating, brushing or printing, such as inkjet printing, screen printing, gravure printing, lithography or mobile printing.
- the present invention discloses various ways of producing an electrode or current directing layer having a voltage difference.
- a thin metal wire can be used to form a two-electrode layout between the two sides of the transparent conductive layer 12 that have the shortest linear distance.
- the electrode can be mainly made of silver paste, and the current can be uniformly passed through the transparent conductive layer 12 to achieve a rapid and uniform temperature rise and fall, and the main method for the silver offset screen electrode comprises screen printing, evaporation, Sputtering, pasting, etc., and electrodes are respectively disposed on the surface of the transparent conductive layer 12 opposite to the substrate layer 11.
- it may be formed on the glass substrate layer 11, and then the transparent conductive layer 12 may be formed on the electrode or the conductive layer forming the electrode.
- the electrodes are disposed on the transparent conductive layer 12 separately from each other, and the conductivity of the electrode is higher than that of the transparent conductive layer 12, for example, silver glue or a high-conductivity metal colloid, in practical applications.
- the colloids may be formed on the transparent conductive layer 12 by coating or printing; preferably, the two electrodes may be respectively disposed on the opposite sides of the transparent conductive layer 12; In the application requirements, they may also be separated from each other and disposed on the adjacent sides of the transparent conductive layer 20. Or an electrode occupies adjacent two sides, respectively.
- the above selection affects the distribution and flow path of the current on the transparent conductive layer 12, thereby determining the distribution of energy consumption, so that the present invention can heat the target surface evenly, or can separately heat up the specific area to overcome the transparency.
- the problem of uneven heating caused by the conductive layer 12 due to uniform coating will be described in detail below.
- the electrode referred to in the present invention is not limited to a layered structure, and in practical applications, it may be replaced with a metal thin wire having a high electrical conductivity as required.
- the transparent conductive layer 12 may be directly formed on the surface of the glass substrate layer 11 by coating or printing, and the electrode may be subsequently coated or printed on the surface. On the transparent conductive layer 12.
- the area of the front windshield of the automobile is large, so that when the same nano metal material is evenly distributed on the transparent conductive layer 12, the whole glass may be heated.
- the temperature is not uniform, and thus the problem of regional defogging rate may occur. Therefore, preferably, the cross-sectional area of the nano metal coating layer that makes the transparent conductive layer 12 adjacent to the current introduction current is small, and the cross-sectional area of the nano metal coating that is far from the current introduction position of the electrode is larger, thereby The heating temperature of the entire glass is made uniform so that the entire glass has the same demisting rate.
- the transparent conductive layer 12 may be patterned by screen printing or etching to form various pattern layers, such as dots, polygons, and staggered lines. Concentric circles or round rows.
- the principle is that the total area of the portion of the transparent conductive layer close to the electrode is lowered to be lower than the portion of the conductive layer located away from the electrode at the center portion for the purpose of averaging the energy distribution so that the planar heating structure can uniformly heat the target plane.
- heating capacity can be increased for a specific area.
- the transmittance of the planar heating structure 1 as a whole can be further increased, thereby satisfying the requirements for window transparency of national automobile exit specifications.
- the whole is in the form of a transparent film, so that it can be attached to the interior of the car, such as the front or rear windshield, etc., and does not hinder the driver's line of sight, achieving rapid and uniform heating.
- the transparent conductive layer 12 disclosed in the present application has the ability to conduct electricity because of the composition of the nano metal raw materials. Compared with Quickclear and the like, it is not easy to generate breakpoints. Due to the full-layer layout of the pattern, there is also an alternative conductive path to compensate for the defect of the single breakpoint when the breakpoint is generated. Therefore, the local defect does not cause the entire transparent conductive layer 12 to lose its working ability, and the process can be greatly reduced. Difficulty, increase yield, and increase product reliability.
- the transparent conductive layer 12 will controllably heat up, so that the glass substrate layer 11 on one side thereof can be heated. Therefore, the mist of the glass substrate layer 11 relative to the outer surface of the transparent conductive layer 12 can be effectively removed, and since the transparent conductive layer 12 and the glass substrate layer 11 are joined by the entire surface, the The transparent conductive layer 12 can quickly heat the glass substrate layer 11, and can effectively raise the temperature of the entire surface of the glass substrate layer 11 evenly, and achieve the effect of defogging while achieving the entire surface.
- 2B is a schematic diagram of heating and raising temperature versus time in an embodiment of the present invention.
- the planar heating structure 12 disclosed in an embodiment of the present invention applies a voltage of 40 volts per
- the temperature can be increased by 12 ° C ⁇ 1 ° C in 2 minutes, that is, the planar heating structure disclosed in one embodiment of the present invention can be quickly charged with a small amount of electricity.
- the glass of the car is heated to achieve the effect of defogging.
- Fig. 2B the reason why the voltage is appropriately increased to increase the temperature is high.
- 40 volts is used as an explanation here, it does not mean that the power supply mode of 20 volts and 30 volts and the corresponding data in the figure are excluded. In fact, FIG. 2B All the data disclosed should be considered as a complete disclosure and will not be repeated here.
- the temperature rise data disclosed in Figure 2B is to ensure that the window glass maintains sufficient light transmittance and haze.
- the completed data for example, while implementing the heating data of FIG. 2B, the planar heating structure 1 can achieve a condition that the light transmittance is greater than 85 percent and the haze is less than 3 percent, and at the same time, the transparent conductive
- the resistance of layer 12 per square centimeter is less than or equal to ten ohms.
- a first protective layer 13 is disposed over the surface of the transparent conductive layer 12.
- the protective layer 13 may be a transparent optical adhesive or may be coated.
- the transparent insulating material that has been removed, or a pre-formed protective layer, is then glued to the transparent conductive layer 12.
- the first protective layer 13 completely covers the transparent conductive layer 12 and the electrodes to provide complete protection of the transparent conductive layer 12 and the electrodes; and the thermal conductivity of the first protective layer 13 is higher than that of the glass substrate layer 11 Therefore, the heat source can be discharged from the glass substrate layer 11 by conduction or radiation only on one side, so that the planar heating structure 1 can achieve rapid and uniform heat generation.
- the first protective layer 13 completely covers the transparent conductive layer 12 to provide the The transparent conductive layer 12 is completely protected.
- the first protective layer 13 may be formed of a PVB (Polyvinyl Butyral Film) film.
- the first protective layer 13 is a hot melt adhesive film, and the material thereof can be selected from a PVB (polyvinyl butyral) film or an EVA (ethylene vinyl acetate copolymer) film.
- FIG. 3 is another embodiment of the present invention based on FIG. 1.
- the wiring of the electrode is clearly visible and affects the visual effect of the window.
- an ink layer 14 is disposed between the glass substrate layer 11 and the transparent conductive layer 12.
- the ink layer 14 is distributed at the position where the electrodes are located, and is formed only on the sides or edges of the transparent conductive layer 12 corresponding to the electrodes to increase the visibility of the planar heating structure.
- the functional structure of the embodiment has been completely disclosed.
- the glass substrate layer 11, the transparent conductive layer 12 and both sides of the first protective layer 13 are exposed to the air as a whole, and the use environment of the automobile may be very harsh.
- the use environment of the automobile may be very harsh.
- it is used in a high temperature, high humidity, and even an atypical environment that promotes oxidation speed such as sulfur.
- a reinforced material may be applied to the glass substrate layer 11
- the transparent conductive layer 12 and at least one side surface of the first protective layer 13 are coated.
- the reinforcing glue can be formed by curing a liquid glue through a curing process.
- the reinforced adhesive has a viscosity of 500 to 1200 mPa/s when uncured, and a hardness of 70 to 85 Shore after curing.
- FIG. 4 is a structural diagram of another planar heating structure 2 disclosed in the present invention.
- the planar heating structure 2 comprises the glass substrate layer 11, the transparent conductive layer 12 and the first protective layer 13, and a second protective layer 15 is additionally added.
- the second protective layer 15 is disposed between the substrate layer 11 and the transparent conductive layer 12, and the second protective layer 15 is an optical functional layer having ultraviolet resistance or / Ability with anti-reflection.
- the ultraviolet protection function of the second protective layer 15 reduces the total amount of ultraviolet light entering the transparent conductive layer 12, thereby prolonging the life of the nano metal in the transparent conductive layer 12 and prolonging the period in which it enters the deteriorated state.
- the anti-reflection function reduces the possibility of the transparent conductive layer 12 and the first protective layer 13 from being reflected, and increases the overall transparency of the planar heating structure 2.
- the particles or the coating agent of the anti-reflective and/or ultraviolet-resistant material may be mixed and applied to the transparent conductive layer 12 when the transparent conductive layer 12 is formed.
- the heating structure is directly formed on the window glass to form an integrated structure.
- This has the advantage of facilitating the production of factory lines, but if the vehicle in use is to be retrofitted or retrofitted with the planar heating structure disclosed in the present invention for defogging/frosting. Or, when the technology that Quickclear and the like encapsulates the metal wire in the two-layer structure fails, the window glass must be replaced, which will result in waste of resources and is not economical.
- another embodiment will be described below in which the heating structure is independent of the window glass, and then the bonding layer is used in combination with the window to enable uniform and rapid defogging of the installed window.
- FIG. 5A is another embodiment of a planar heating structure attached to a glass according to the present invention, wherein a planar heating structure 3 includes a flexible substrate layer 31 , the transparent conductive layer 12 , The first protective layer 13, an adhesive layer 32, and a release mold 34.
- the transparent conductive layer 12 is disposed on the flexible substrate layer and receives a voltage to consume electrical energy to generate thermal energy.
- the release mold 34 is formed on a surface of the adhesive layer 32 away from the nano metal transparent conductive layer for protecting and shielding the adhesive layer 32.
- the adhesive layer 32 is not attached to the window glass and is attached to the adhesive layer 32. It protects and shields the adhesive layer 32 from accidental sticking and maintains its tack.
- the flexible substrate layer 31 applied in this embodiment needs to accommodate a large deformation amount in order to fit the pattern assembled in a pasting manner.
- the material selection here should be mainly a flexible film, or a composite film of a transparent film to meet the requirements of strength and shape variables.
- the material selection for the transparent flexible film may be selected from one or a combination of the following types of plastic materials: PP, PE, PS, PMMA, PC, PET, PVC, PI, PU, etc. Material. It should be noted here that since the substrate layer 31 is exposed to the user in contact with the user, there is a certain requirement for the wear resistance, and the base layer 31 can be subjected to wear treatment when necessary. To increase the wear resistance and scratch resistance of the substrate layer.
- the adhesive layer 32 is formed or disposed on the transparent conductive layer 12, and the adhesive layer has considerable viscosity for conforming and completely integrating the planar heating structure 3 with the window glass, so that the planar heating structure 3 can
- the vehicle window is uniformly heated and defoamed under the working principle disclosed above.
- a general adhesive layer for a window can be selected, and the adhesive liquid or adhesive can be applied to the window glass by subsequent processing or coating, and then bonded.
- the planar heating structure 3 may also omit the adhesive layer structure if the post-coating method is selected.
- the adhesive layer or the adhesive in order to allow the thermal energy generated by the planar heating structure 3 to be transmitted to the window glass without damage and maintaining the design distribution, the adhesive layer or the adhesive must select a formulation and material having a small thermal resistance to avoid affecting The planar heating structure 3 has a defogging effect.
- the first protective layer 13 is formed between the transparent conductive layer and the adhesive layer, that is, the transparent conductive layer is away from a surface of the substrate layer, and the first protective layer can be bonded thereto.
- the layers are integrated to form a first protective layer with a bonding ability.
- the first protective layer can also function as an optical functional layer, having ultraviolet and/or anti-reflection resistance, and adding a material that absorbs visible light and absorbs heat.
- the first protective layer may be formed on the other surface of the transparent conductive layer adjacent to the substrate layer.
- FIG. 5B is another embodiment based on FIG. 5A.
- the wiring of the electrode is clearly visible and affects the visual effect of the window.
- an ink layer 33 is disposed on the bonding surface of the adhesive layer 32 and the window glass.
- the ink layer 33 is distributed along the position where the electrodes are located, and is formed only on the sides or edges of the transparent conductive layer 12 corresponding to the electrodes to increase the visibility of the planar heating structure.
- FIG. 6 is a structural diagram of another planar heating structure 4 disclosed in the present invention.
- the planar heating structure 4 includes the flexible substrate layer 31, the transparent conductive layer 12, the adhesive layer 32, and the first protective layer 13, and a second protective layer 15 is additionally added.
- the second protective layer 15 is disposed between the adhesive layer 11 and the transparent conductive layer 12, and the second protective layer 15 is an optical functional layer having ultraviolet resistance or / Ability with anti-reflection.
- the ultraviolet protection function of the second protective layer 15 reduces the total amount of ultraviolet light entering the transparent conductive layer 12, thereby prolonging the life of the nano metal in the transparent conductive layer 12 and prolonging the period in which it enters the deteriorated state.
- the anti-reflection function reduces the possibility of the transparent conductive layer 12 and the first protective layer 13 from being reflected, and increases the overall transparency of the planar heating structure 2.
- FIG. 7 is a schematic view showing the combination of a heating structure and a window glass according to another embodiment of the present invention.
- the heating structure is formed separately from the window glass, and then bonded to the window by an adhesive layer. It can be seen here that an ink layer is pre-formed on the window glass to shield the electrodes that supply power to the transparent conductive structure.
- the particles or the coating agent of the anti-reflective and/or ultraviolet-resistant material may be mixed and applied to the transparent conductive layer 12 when the transparent conductive layer 12 is formed.
- the particles or the coating agent of the anti-reflective and/or ultraviolet-resistant material are mixed and applied to the adhesive layer 32 at the time of forming the adhesive layer 32.
- the planar heating structure 1 disclosed in the present application can achieve a condition that the light transmittance is greater than 85 percent and the haze is less than 3 percent. Due to its excellent transparency, it can be used for glass defogging or defrosting of various vehicles such as automobiles, ships and aircraft. In the use of automotive window glass, it can be applied to other parts of the rear windshield, including the front windshield.
- the planar heating structure of the invention can uniformly heat the target and has good visibility and can quickly increase the temperature to a default temperature compared with the prior art, and the planar heating structure can achieve a transmittance of more than 8%. Fifteen, the haze is less than three percent. Due to its excellent transparency, it can be used for glass defogging or defrosting of various vehicles such as automobiles, ships and aircraft. In the use of automotive window glass, it can be applied to other parts of the rear windshield, including the front windshield.
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Abstract
Description
Claims (45)
- 一种平面加热结构,其特征在于,包括:一玻璃基材层;一纳米金属透明导电层,具有多个纳米金属丝,设置于该玻璃基材层上,并接收一电能以转换为热能,其中该等纳米金属丝中,长度大于5μm的该等纳米金属丝比例大于92%;以及一第一保护层,设置于该纳米金属透明导电层上,并完全覆盖该纳米金属透明导电层。
- 如权利要求1所述的该平面加热结构,其特征在于,该等纳米金属丝的纵横比介于10至100之间。
- 如权利要求1所述的该平面加热结构,其特征在于,该纳米金属透明导电层的临限表面负载位准位于0.05μg/每平方公分至10μg/每平方公分之间。
- 如权利要求1所述的该平面加热结构,其特征在于,该平面加热结构满足透光率大于百分之八十五,雾度小于百分之三的条件。
- 如权利要求1所述的平面加热结构,其特征在于,该第一保护层具有以下化合物中的任一成分及其组合:分子量不大于500的有机小分子、具有2-100个单体的寡聚物或大于100个单体的聚合物,任一该等化合物的沸点不小于150℃。
- 如权利要求1所述的该平面加热结构,其特征在于,该纳米金属透明导电层更包含一基质层,该基质层设置于该玻璃基材层上以供该等纳米金属线附着,该基质层的厚度为10nm至5μm,折射率位于1.3至2.5间。
- 如权利要求1所述的该平面加热结构,其特征在于,更包含两电极,位于该平面加热结构相对位置最短的两对侧,一电压被施加于该两电极间。
- 如权利要求7所述的该平面加热结构,其特征在于,当该电压为40伏特时,该平面加热结构的于每平方公分表面积耗能0.07W的状况下,于2分钟内使温度升高12℃±1℃。
- 如权利要求1所述的该平面加热结构,其特征在于,该等纳米金属丝形成下述的图案层及其组合:网点、多角形、交错线列、同心圆或类圆排列。
- 如权利要求1所述的该平面加热结构,其特征在于,该第一保护层的导热系数较该玻璃基材层为低,使电能转换的热能大部分由该玻璃基材层处以传导或辐射方式放出。
- 如权利要求5所述的该平面加热结构,其特征在于,该第一保护层所包含的化合物为下列的一者及其组合:铑盐、锌以及镉盐。
- 如权利要求5所述的该平面加热结构,其特征在于,该第一保护层所包含的化合物为下列的一者及其组合:抗坏血酸钠盐、抗坏血酸钾盐以及抗坏血酸。
- 如权利要求1所述的平面加热结构,其特征在于,更包括:一第二保护层,设置于该玻璃基材层和该纳米金属透明导电层之间,其中该第二保护层具有以下化合物中的任一成分及其组合:分子量不大于500的有机小分子、具有2-100个单体的寡聚物或大于100个单体的聚合物,任一该等化合物的沸点不小于150℃。
- 如权利要求13所述的平面加热结构,其特征在于,该第二保护层所包含的化合物为下列的一者及其组合:铑盐、锌、镉盐、抗坏血酸钠盐、抗坏血酸钾盐以及抗坏血酸。
- 如权利要求7所述的平面加热结构,其特征在于,进一步包括:一油墨层,形成于该玻璃基材层靠近该纳米金属透明导电层的一表面,该油墨层遮蔽该等电极以避免视觉干扰。
- 如权利要求1所述的平面加热结构,其特征在于,该第一保护层是直接形成或通过一粘合层贴合于该纳米金属透明导电层远离该玻璃基材层的一表面。
- 如权利要求1所述的平面加热结构,其特征在于,进一步包括:一光学功能层,设置于该玻璃基材层与该纳米金属透明导电层之间。
- 如权利要求1所述的平面加热结构,其特征在于,该纳米金属透明导电层内包括抗反射以及/或抗紫外线材料的粒子或涂剂。
- 如权利要求1所述的平面加热结构,其特征在于,进一步包括:一加固胶,形成于该平面加热结构的至少一外侧面,并且至少包覆该基材层、该纳米金属透明导电层及该第一保护层的侧面。
- 如权利要求19所述的平面加热结构,其特征在于,该加固胶的材质为 一液态胶,经由一固化过程而固化形成。
- 如权利要求20所述的平面加热结构,其特征在于,该加固胶在未固化时的粘度为500~1200毫帕·秒,固化后的硬度为肖氏D 70~85。
- 如权利要求1所述的平面加热结构,其特征在于,该等纳米金属丝为下列材料的一者及其组合:银、金、铜、镍及镀金银。
- 一种贴合于玻璃的平面加热结构,其特征在于,包括:一挠性基材层;一纳米金属透明导电层,具有多个纳米金属丝,设置于该挠性基材层上,并接收一电能以转换为热能,其中该等纳米金属丝中,长度大于5μm的该等纳米金属丝比例大于92%;一粘合层,设置于该纳米金属透明导电层上;以及一离型膜,形成于该粘合层远离该纳米金属透明导电层的一表面。
- 如权利要求23所述的该平面加热结构,其特征在于,更包括一第一保护层,该第一保护层设置于该纳米金属透明导电层上,并完全覆盖该纳米金属透明导电层。
- 如权利要求23所述的该平面加热结构,其特征在于,该挠性基材层为下列材料的一者及其组合:PP、PE、PS、PMMA、PC、PET、PVC、PI以及PU。
- 如权利要求23所述的该平面加热结构,其特征在于,该等纳米金属丝的纵横比介于10至100之间。
- 如权利要求23所述的该平面加热结构,其特征在于,该纳米金属透明导电层的临限表面负载位准位于0.05μg/每平方公分至10μg/每平方公分之间。
- 如权利要求23所述的该平面加热结构,其特征在于,该平面加热结构满足透光率大于百分之八十五,雾度小于百分之三的条件。
- 如权利要求24所述的平面加热结构,其特征在于,该第一保护层具有以下化合物中的任一成分及其组合:分子量不大于500的有机小分子、具有2-100个单体的寡聚物或大于100个单体的聚合物,任一该等化合物的沸点不小于150℃。
- 如权利要求23所述的该平面加热结构,其特征在于,该纳米金属透明导电层更包含一基质层,该基质层设置于该挠性基材层上以供该等纳米金属线 附着,该基质层的厚度为10nm至5μm,折射率位于1.3至2.5间。
- 如权利要求23所述的该平面加热结构,其特征在于,更包含两电极,位于该平面加热结构相对位置最短的两对侧,一电压被施加于该两电极间。
- 如权利要求31所述的该平面加热结构,其特征在于,当该电压为40伏特时,该平面加热结构的于每平方公分表面积耗能0.07W的状况下,于2分钟内使温度升高12℃±1℃。
- 如权利要求23所述的该平面加热结构,其特征在于,该等纳米金属丝形成下述的图案层及其组合:网点、多角形、交错线列、同心圆或类圆排列。
- 如权利要求24所述的该平面加热结构,其特征在于,该第一保护层的导热系数较该挠性基材层为低,使电能转换的热能大部分由该挠性基材层处以传导或辐射方式放出。
- 如权利要求29所述的该平面加热结构,其特征在于,该第一保护层所包含的化合物为下列的一者及其组合:铑盐、锌以及镉盐。
- 如权利要求29所述的该平面加热结构,其特征在于,该第一保护层所包含的化合物为下列的一者及其组合:抗坏血酸钠盐、抗坏血酸钾盐以及抗坏血酸。
- 如权利要求24所述的平面加热结构,其特征在于,更包括:一第二保护层,设置于该挠性基材层和该纳米金属透明导电层之间,其中该第二保护层具有以下化合物中的任一成分及其组合:分子量不大于500的有机小分子、具有2-100个单体的寡聚物或大于100个单体的聚合物,任一该等化合物的沸点不小于150℃。
- 如权利要求37所述的平面加热结构,其特征在于,该第二保护层所包含的化合物为下列的一者及其组合:铑盐、锌、镉盐、抗坏血酸钠盐、抗坏血酸钾盐以及抗坏血酸。
- 如权利要求23所述的平面加热结构,其特征在于,进一步包括:一油墨层,形成于该挠性基材层靠近该纳米金属透明导电层的一表面,该油墨层遮蔽该等电极以避免视觉干扰。
- 如权利要求23所述的平面加热结构,其特征在于,进一步包括:一光学功能层,设置于该挠性基材层与该纳米金属透明导电层之间。
- 如权利要求23所述的平面加热结构,其特征在于,该纳米金属透明导 电层内包括抗反射以及/或抗紫外线材料的粒子或涂剂。
- 如权利要求23所述的平面加热结构,其特征在于,进一步包括:一加固胶,形成于该平面加热结构的至少一外侧面,并且至少包覆该基材层、该纳米金属透明导电层及该第一保护层的侧面。
- 如权利要求42所述的平面加热结构,其特征在于,该加固胶的材质为一液态胶,经由一固化过程而固化形成。
- 如权利要求43所述的平面加热结构,其特征在于,该加固胶在未固化时的粘度为500~1200毫帕·秒,固化后的硬度为肖氏D 70~85。
- 如权利要求23所述的平面加热结构,其特征在于,该等纳米金属丝为下列材料的一者及其组合:银、金、铜、镍及镀金银。
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104053256A (zh) * | 2014-05-14 | 2014-09-17 | 中国科学院合肥物质科学研究院 | 基于银纳米线透明导电薄膜的加热器及其制备方法 |
CN104616837A (zh) * | 2015-02-02 | 2015-05-13 | 华南师范大学 | 平面有序化的金属纳米线叠层透明导电薄膜及其制备方法 |
US9061481B2 (en) * | 2008-10-07 | 2015-06-23 | Guardian Industires Corp. | Display-on-demand mirror with optional defogging feature, and method of making the same |
CN104992752A (zh) * | 2015-07-16 | 2015-10-21 | 城步新鼎盛电子科技有限公司 | 一种纳米银线透明导电薄膜的生产方法 |
CN105981473A (zh) * | 2013-12-16 | 2016-09-28 | 法国圣戈班玻璃厂 | 具有高频透射率的可加热的窗玻璃 |
CN106465478A (zh) * | 2014-08-08 | 2017-02-22 | 法国圣戈班玻璃厂 | 具有电加热层的透明玻璃板、其制造方法及其用途 |
CN106448824A (zh) * | 2016-10-17 | 2017-02-22 | 北京石油化工学院 | 一种透明导电薄膜及其制备方法与应用 |
CN106457774A (zh) * | 2014-07-01 | 2017-02-22 | 法国圣戈班玻璃厂 | 可加热的层压侧玻璃板 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62459U (zh) * | 1985-06-20 | 1987-01-06 | ||
DE3522623A1 (de) | 1985-06-25 | 1987-01-08 | Bayer Ag | Tetramethylcyclopropancarbonsaeureester |
JPH0492397U (zh) * | 1990-12-28 | 1992-08-11 | ||
KR102103541B1 (ko) * | 2005-08-12 | 2020-04-23 | 캄브리오스 필름 솔루션스 코포레이션 | 나노와이어 기반의 투명 도전체 |
US20090321364A1 (en) * | 2007-04-20 | 2009-12-31 | Cambrios Technologies Corporation | Systems and methods for filtering nanowires |
US9266307B2 (en) * | 2008-09-10 | 2016-02-23 | Solutia Inc. | Heated multiple layer glazings |
JP2010103041A (ja) * | 2008-10-27 | 2010-05-06 | Konica Minolta Holdings Inc | 透明フィルムヒーター、ヒーター機能付きガラス、ヒーター機能付き合わせガラスおよび自動車用窓ガラス |
JP5667195B2 (ja) * | 2009-09-29 | 2015-02-12 | 3533899 インコーポレーティッド | 有機電子デバイス、組成物、および方法 |
JP2011090878A (ja) * | 2009-10-22 | 2011-05-06 | Fujifilm Corp | 透明導電体の製造方法 |
KR101201053B1 (ko) * | 2012-04-16 | 2012-11-14 | 김선일 | 면상발열체의 제조방법 및 그 방법에 의하여 제조된 면상발열체 |
US9920207B2 (en) * | 2012-06-22 | 2018-03-20 | C3Nano Inc. | Metal nanostructured networks and transparent conductive material |
JP6588829B2 (ja) * | 2013-02-15 | 2019-10-09 | カンブリオス フィルム ソリューションズ コーポレーション | 光学スタック |
CN203974158U (zh) * | 2014-04-25 | 2014-12-03 | 无锡格菲电子薄膜科技有限公司 | 具有除雾除霜功能的防爆隔热膜 |
JP6530389B2 (ja) * | 2014-06-09 | 2019-06-12 | 美津子 馬場 | 発熱体 |
CN204183984U (zh) * | 2014-10-24 | 2015-03-04 | 林行 | 一种具有电加热功能的汽车玻璃贴膜 |
JP2016119305A (ja) * | 2014-12-19 | 2016-06-30 | 出光興産株式会社 | 組成物、当該組成物から得られる導電体 |
CN107113920A (zh) * | 2014-12-31 | 2017-08-29 | 可隆工业株式会社 | 透明面状发热体 |
KR101637920B1 (ko) * | 2015-01-06 | 2016-07-08 | 연세대학교 산학협력단 | 투명필름히터 및 그의 제조방법 |
-
2017
- 2017-03-24 CN CN201710183435.8A patent/CN108621753A/zh active Pending
-
2018
- 2018-03-23 EP EP18771474.6A patent/EP3606283A4/en not_active Withdrawn
- 2018-03-23 JP JP2020500952A patent/JP6961145B2/ja active Active
- 2018-03-23 WO PCT/CN2018/080257 patent/WO2018171731A1/zh active Search and Examination
- 2018-03-23 KR KR1020197031558A patent/KR20190127928A/ko not_active Ceased
-
2019
- 2019-09-24 US US16/580,357 patent/US11432378B2/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9061481B2 (en) * | 2008-10-07 | 2015-06-23 | Guardian Industires Corp. | Display-on-demand mirror with optional defogging feature, and method of making the same |
CN105981473A (zh) * | 2013-12-16 | 2016-09-28 | 法国圣戈班玻璃厂 | 具有高频透射率的可加热的窗玻璃 |
CN104053256A (zh) * | 2014-05-14 | 2014-09-17 | 中国科学院合肥物质科学研究院 | 基于银纳米线透明导电薄膜的加热器及其制备方法 |
CN106457774A (zh) * | 2014-07-01 | 2017-02-22 | 法国圣戈班玻璃厂 | 可加热的层压侧玻璃板 |
CN106465478A (zh) * | 2014-08-08 | 2017-02-22 | 法国圣戈班玻璃厂 | 具有电加热层的透明玻璃板、其制造方法及其用途 |
CN104616837A (zh) * | 2015-02-02 | 2015-05-13 | 华南师范大学 | 平面有序化的金属纳米线叠层透明导电薄膜及其制备方法 |
CN104992752A (zh) * | 2015-07-16 | 2015-10-21 | 城步新鼎盛电子科技有限公司 | 一种纳米银线透明导电薄膜的生产方法 |
CN106448824A (zh) * | 2016-10-17 | 2017-02-22 | 北京石油化工学院 | 一种透明导电薄膜及其制备方法与应用 |
Non-Patent Citations (1)
Title |
---|
See also references of EP3606283A4 * |
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