WO2002098996A1 - Radiative cooling surface coatings - Google Patents

Radiative cooling surface coatings Download PDF

Info

Publication number
WO2002098996A1
WO2002098996A1 PCT/AU2002/000695 AU0200695W WO02098996A1 WO 2002098996 A1 WO2002098996 A1 WO 2002098996A1 AU 0200695 W AU0200695 W AU 0200695W WO 02098996 A1 WO02098996 A1 WO 02098996A1
Authority
WO
WIPO (PCT)
Prior art keywords
microspheres
roof
coating
composition according
surface coating
Prior art date
Application number
PCT/AU2002/000695
Other languages
French (fr)
Other versions
WO2002098996B1 (en
Inventor
Conrad Stephen Wojtysiak
Original Assignee
Lehmann Pacific Solar Pty Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lehmann Pacific Solar Pty Limited filed Critical Lehmann Pacific Solar Pty Limited
Priority to EP02729636A priority Critical patent/EP1409596A4/en
Priority to AU2002302177A priority patent/AU2002302177B2/en
Priority to CN028126017A priority patent/CN1518582B/en
Priority to JP2003502108A priority patent/JP2004532919A/en
Priority to US10/479,835 priority patent/US7503971B2/en
Publication of WO2002098996A1 publication Critical patent/WO2002098996A1/en
Publication of WO2002098996B1 publication Critical patent/WO2002098996B1/en
Priority to ZA2004/02724A priority patent/ZA200402724B/en

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04DROOF COVERINGS; SKY-LIGHTS; GUTTERS; ROOF-WORKING TOOLS
    • E04D7/00Roof covering exclusively consisting of sealing masses applied in situ; Gravelling of flat roofs
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/66Additives characterised by particle size
    • C09D7/69Particle size larger than 1000 nm
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/70Additives characterised by shape, e.g. fibres, flakes or microspheres
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/02Ingredients treated with inorganic substances
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F28HEAT EXCHANGE IN GENERAL
    • F28FDETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
    • F28F2245/00Coatings; Surface treatments
    • F28F2245/06Coatings; Surface treatments having particular radiating, reflecting or absorbing features, e.g. for improving heat transfer by radiation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A30/00Adapting or protecting infrastructure or their operation
    • Y02A30/24Structural elements or technologies for improving thermal insulation
    • Y02A30/254Roof garden systems; Roof coverings with high solar reflectance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02BCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B80/00Architectural or constructional elements improving the thermal performance of buildings

Definitions

  • This invention relates to surface coatings having radiative cooling properties and in particular to the use of such coatings on external surfaces of buildings to reduce the heat load to those buildings.
  • Radiative cooling refers to the process whereby a body will emit as radiation heat energy absorbed through normal convection and conduction processes .
  • the physics of black body radiation states that the wavelength at which a body will emit radiation is dependent on its temperature. For terrestrial temperatures, emission occurs in the infra-red (IR) wavelengths with a peak emission at approximately 11.4 ⁇ m. Incident solar radiation, on the other hand, corresponds to a black body temperature of 6000° K and is concentrated in the ultra-violet, visible and near IR wavelengths.
  • IR infra-red
  • Fig. 1 shows atmospheric absorption as a function of wavelength.
  • the species responsible for the various absorption peaks are identified on the horizontal axis.
  • Conversely, for the wavelengths corresponding to these atmospheric windows there will be little radiation in the atmosphere as the majority of radiation emitted by the Earth at these wavelengths is allowed to pass through the atmosphere to space.
  • a “selective surface” is one that exploits the atmospheric window by preferentially emitting thermal energy at wavelengths corresponding to these atmospheric windows where there is reduced incident radiation which may be absorbed by the surface, that allow rapid transfer of that radiation to space and by being non-absorptive of radiation outside these wavelengths.
  • the invention resides in a curable formulation for use as a radiative cooling surface coating for an external surface of a building characterised by low absorption at wavelengths of incident solar radiation and high radiative emittance at wavelengths of reduced incident radiation.
  • the invention is based on the discovery that such a coating may be obtained by the inclusion of a dispersion of gas or vacuum filled microspheres in a coating composition containing a solar reflective pigment.
  • the microspheres employed are preferably of the silica type, most preferably having a shell of silica-alumina. Coatings according to the invention, incorporating effective amounts of such microspheres, have in fact demonstrated the ability to achieve below-ambient temperatures in the interior of coated structures,
  • microspheres employed in such coatings may be gas filled, for example with CO 2 or N 2 ⁇ or they may be vacuum filled.
  • the coating is not only non-absorptive of solar radiation but is reflective, rather than transmissive, of these wavelengths.
  • the coating has a solar reflectance greater than 80% and more preferably greater than 84%.
  • the coating is characterised by radiative emittance ( ⁇ ) greater than 85 %, more preferably greater than 90% and still more preferably greater than 95% at thermal wavelengths.
  • the combined effect of the solar absorption and radiative emittance characteristics of the coating are such that the coating is able to absorb heat energy from within an internal air space and re-radiate that energy as thermal radiation to achieve net radiative cooling of the air space.
  • the coating of the invention when applied to a sheet steel surface exposed to solar radiation at Air Mass 1.5 Solar Spectrum and ambient temperature of 20-28 °C the formulation displays a net radiative cooling effect to the air space below the steel sheet.
  • the formulation of the invention is curable and may be applied to an existing building using a large area spray process.
  • Fig. 1 shows a graph of atmospheric absorption versus wavelength
  • Fig. 2 shows the results of comparative testing of a coating according to the invention against conventional roofing systems
  • Figs. 3 to 5 show the results of further comparative testing of the invention DESCRIPTION OF PREFERRED EMBODIMENTS OF THE INVENTION
  • a formulation according to the invention was manufactured as follows. Quantities given are for a total 600 L mix and are provided for illustrative purposes only. Though precise quantities are stated, wide variation from these quantities, even down to zero for some components, are possible and within the scope of the invention.
  • 610 g of a sequestrating and wetting agent preferably a polyphosphate and 610g of a dispersing agent was added to 91 L of water in a mixing drum and mixed at 2000rpm for 10 minutes or until the ingredients are thoroughly dispersed.
  • a solar reflective pigment such as rutile grade Titanium Oxide (TiO 2 ) (38kg)
  • 72 kg of a filler such as CaCO 2 or MgCO 2 that lends water resistance to the cured formulation
  • 72 kg of a suspension agent e.g. MgSiO 3 , BaSO or SiO 2 that is also abrasion and corrosion resistant on metals.
  • the mix was then dispersed at approx 2000 rpm for 1 hour. The actual mixing times will depend on the particle size. It is preferred that mixing continues until the mixture is brought to a Hegman setting of 7 giving about 15 microns measured on a Hegman Grind Gauge.
  • Approx 228 L of a binder such as a styrene acrylic, acrylic resin, homopolymer or PVA was then added and mixed for 15 minutes at 1500 rpm.
  • coalescing agent such as any trimethylpentandiol, e.g. Isonol (4.8L) and mixed for 15 minutes at 1100 rpm.
  • a coalescing agent such as any trimethylpentandiol, e.g. Isonol (4.8L) and mixed for 15 minutes at 1100 rpm.
  • Propylene Glycol or other suitable glycols that act as a further coalescing agent and adjust the curing time were added and mixed for 5-10 minutes at 1100 rpm.
  • the biocide may include a uni-fungicide, bactericide, insecticide and algaecide and is preferably devoid of heavy metals.
  • a thickening agent preferably selected from the hydroxycellulose group (630 g) was pre-dissolved in 10 L of water and then added and mixed into the main mixture for 10- 15 minutes at 1100 rpm. The mixture thickened with the addition of this component. The viscosity was measured using a No. 4 Ford Cup and adjusted until a run through time of 35 seconds was achieved with allowances made temperature.
  • the final mixing step was to add a microspheres component, in this example 70-90 kg, which was mixed for approx 30 minutes at a reduced rate of 200-300 rpm to avoid damage to the spheres.
  • the microspheres were approximately 45 ⁇ m - 150 ⁇ m in diameter (average 50 ⁇ m is preferred) having a silica-alumina shell between 0.3 ⁇ m and 1 ⁇ m thick and a filling of CO 2 .
  • the spheres form a fine light powder and are believed to enhance the emissivity of the coating at least in the wavelengths of the atmospheric windows. While CO 2 -filled microspheres were used in this example, the spheres can be vacuum filled to a pressure of 4 Torr or can be filled with another gas, for example N 2 .
  • the above ingredients other than the microspheres were chosen from those available primarily for their low solar abso ⁇ tion and high thermal emittance properties as well as for their properties that make them suitable for use as a roof coating, e.g. fire retardant, corrosion resistance, biocide etc.
  • a relatively small quantity of white pigment (TiO ) is employed, and this can be increased where appropriate.
  • Coating compositions containing greater concentrations of microspheres for example 140 Kg per 600 1, can be used to advantage. Higher concentrations, for example 150 Kg per 600 1, may also be used.
  • the preferred composition has at least 40% solids, more preferably at least 60% solids and still more preferably at least 70% solids.
  • the resultant mixture can be sealed and stored ready for application.
  • the composition can be coated onto any exterior surface but is preferably applied to roofs that have a clear view of the sky to ensure maximum radiative cooling.
  • a large area coating e.g. on a warehouse roof, is best achieved by a spray coating process, for example using a GracoTM airless spray gun with Tungsten Carbide tip.
  • the coating may be applied as a single thick layer but will more typically be built up from a series of thin layers.
  • the thickness at which a single layer of the coating can be applied will depend on the viscosity of the formulation and the flatness of the surface. A sloping, undulating or rough surface will require the application of thinner coats to ensure the overall coating is of even thickness across the surface.
  • the coating is too thick it may act as a blanket for the building and retard the transfer of heat from the internal air space to the coating for radiative emission resulting in higher interior temperatures. It is thus preferred that the thickness of the coating is less than 10mm.
  • Coatings manufactured in accordance with the above example have been found by optical measurement to exhibit a hemispherical solar absorptance of 0.15, and thermal emittance estimated from measured roof heat loss coefficients is greater that 0.9.
  • the observed radiative capability and IR spectra of the material are such, however, as to indicate the existence of selective radiative ability in the 8 to 13 ⁇ m atmospheric window.
  • Comparative tests have been conducted between the composition of the invention and conventional roofing systems.
  • four steel boxes approx 330mm x 330 mm * 760mm, open at one end, were used in the tests.
  • the boxes were inverted (i.e. open end down) so that the bottom of the box became the roof for the purpose of the test.
  • Two boxes had outer surfaces of bare steel, and one of these had the underside of its roof insulated with the same batts as used on the walls.
  • the third box was of off- white Colorbond steel, and the remaining box had the exterior side of its roof coated to a thickness of approx 0.7 mm with the composition of the invention, prepared as above.
  • test boxes were disposed outside with each box having a clear view of the sky. Internal temperature readings were taken hourly for a period of 10 days. Ambient outside temperatures were also recorded. The results are graphed in Fig. 2 where the composition of the invention is referenced using the present applicant's trade mark InsulshieldTM. As is evident from the results, the coatings of the invention performed remarkably better than the existing roofing systems in maintaining a low temperature in the interior space of the test box and was the only product to consistently provide interior space temperatures below ambient.
  • test period covered predominantly cloudless days and nights and that under more overcast conditions the performance of the coatings of the invention is reduced. However, even under these conditions, the coatings of the invention still out performed the prior art systems.
  • an uninsulated steel enclosure was coated with a formulation of the invention, allowed to cure and then subjected to solar radiation at 1062 Wm " incident on the horizontal at ambient temperature of 23 °C with clear sky conditions.
  • the total radiation energy off the roof of the enclosure comprised 894 Wm "2 of reflected solar energy and 188 Wm "2 of re-radiated heat (IR).
  • the total energy output of 1082 Wm '2 was thus greater than the incident solar energy. This suggests that the coated roof was able to absorb heat energy from the air space within the enclosure and output that energy to the atmosphere.
  • the net energy output was 1064 Wm " which is less than for the uninsulated case but is still sufficient to achieve a small net cooling effect, even in conditions of high incident solar radiation.
  • the internal temperature in the uninsulated enclosure was 16.4 °C compared with 20°C ambient and at 2 am the internal temperature was 15.7°C compared with 18.8°C ambient. In the insulated case, the internal temperatures were slightly above ambient.
  • the coating of the invention is intended principally for the commercial and industrial metal-roofed buildings which generally have a much larger roof area than exterior wall surfaces area.
  • the demountable classrooms present a "worst case scenario" in which to trial the coating for the following reasons:- low roof to wall ratio, unlike supermarkets or warehouses, sub-roof insulation, which delays internal heat reaching the coating thereby creating a time lag when compared to ambient air temperature movements, a relatively high occupancy rate of about 3m 2 per person, which is about twice the density of a standard supermarket, open windows and ceiling fans that permit a high rate of external air exchange thereby increasing the difficulty for the coating to maintain internal temperatures constantly below ambient.
  • the coating performed extraordinarily well.
  • the maximum daily temperature of the coated room during the occupied period of the trial (February to April, 2001) was maintained at or below ambient for 84% of the time.
  • the coated room's peak temperature was at or below ambient 81% of the time, with differing weather conditions accounting for the variation.
  • Temperature recorders were located adjacent to the teacher's blackboard at a height to correctly record the temperature of the occupied portion of the room.
  • the graphs of Figs. 5 - 6 show the results of observations in two rooms used in the test, one of which was roof-coated with the composition of the invention. (Another uncoated room contained a small window-mounted air conditioning unit, and there was no control over its use. The unit was, however, at the end of the classroom remote from the temperature sensor, and in fact the corresponding graphs for this room show that it had no appreciable affect on the measured temperature. The graphs for that room are therefore not included here).
  • the rooms had shaded walls, while their roofs were not affected by any shading factors.
  • Fig. 3 Also apparent from Fig. 3 is the fact that the coated room commenced cooling usually when ambient temperature fell to that of the coated room. As noted above, the time lag in the cooling of the coated room would be primarily due to the sub-roof insulation trapping internal heat which would have entered the building through air exchange or being generated from internal sources including people.
  • the coated room maintained the more even flow of temperatures, While it was considerably cooler than the other rooms as well as ambient air, it also did not get as cold overnight.
  • the coated room was about 4°C to 7°C cooler than ambient and the other rooms.
  • April 17th is a case in point.
  • the coated room is still only 18°C and ambient is 23°C.
  • ambient peaks at 12:00 p.m. it reaches 28°C, while the coated room is still a comfortable 22°C.
  • the coated room eventually reached only 25.5°C around 6 p.m., long after the room was no longer in use for the day.
  • Fig. 5 shows that for 84% of the occupied period the coated room was at or below the maximum ambient temperature and almost always well below the other rooms.
  • the days on which the coated room was slightly higher than ambient are the coolest days, when there was predominant cloud cover since the coating requires a mainly clear sky to operate. This is the ideal - in cooler or cloudy weather it is usually desirable to retain a little more internal heat.
  • the radiative cooling coatings of the invention are most effective when used on roofs without underlying batt insulation. It is believed that the batt insulation, while providing a barrier to the ingress of absorbed solar radiation, retards the radiative cooling mechanism by reducing the transport of heat energy from the internal air space to the coating when it can be radiated to the atmosphere.
  • Coatings according to the invention provide a useful alternative to conventional methods for dealing with solar heat loads. However, the suitability of their use will very much depend on the environment in which they are to be employed. The coatings will be most suitable for use on buildings where the summer time cooling costs are greater than the winter time heating costs. While the experiments to date indicate that the coatings are best used on roofs without underlying insulation, the economics of the situation may dictate that due to winter heating considerations it is best that insulation is used.
  • the benefits of the invention include that less reliance can be placed on air conditioning to maintain low temperatures within an air space thus leading to reduced energy consumption. This has advantages for the local system in which the invention is utilised as well as wider environmental advantages including reduced production of greenhouse gases.
  • the formulation of the invention may include additional components such as a biocide, fire retardant, corrosion retardant etc. or alternatively, the previously described components can be selected for these properties.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Architecture (AREA)
  • Civil Engineering (AREA)
  • Structural Engineering (AREA)
  • Nanotechnology (AREA)
  • Paints Or Removers (AREA)
  • Building Environments (AREA)

Abstract

A surface coating composition which exhibits low solar absorption and preferential emission at wavelengths corresponding to atmospheric windows in the infra-red regions is provided by the addition of microspheres to a composition containing a solar reflective pigment.

Description

RADIATIVE COOLING SURFACE COATINGS
BACKGROUND TO THE INVENTION
This invention relates to surface coatings having radiative cooling properties and in particular to the use of such coatings on external surfaces of buildings to reduce the heat load to those buildings.
Radiative cooling refers to the process whereby a body will emit as radiation heat energy absorbed through normal convection and conduction processes .
The physics of black body radiation states that the wavelength at which a body will emit radiation is dependent on its temperature. For terrestrial temperatures, emission occurs in the infra-red (IR) wavelengths with a peak emission at approximately 11.4 μm. Incident solar radiation, on the other hand, corresponds to a black body temperature of 6000° K and is concentrated in the ultra-violet, visible and near IR wavelengths.
Not all of the radiation emitted by the Earth passes through to space. A significant portion of this radiation is absorbed in the Earth's atmosphere, particularly by the so- called "greenhouse gases" water vapour, carbon dioxide and ozone, and re-emitted back to the Earth's surface.
Fig. 1 shows atmospheric absorption as a function of wavelength. The species responsible for the various absorption peaks are identified on the horizontal axis. There is a low absorption "atmospheric window" in the region of 8-13 μm where the atmosphere is relatively transparent. A similar window exists for some wavelengths within the 1-5 μm band. Radiation from the Earth's surface within these wavelengths is likely to pass through these atmospheric windows to space rather than absorbed by the atmosphere and returned to the Earth's surface. For the wavelengths having high atmospheric absorption there will be significant amounts of radiation in the atmosphere as that radiation is absorbed and re-emitted back to Earth. Conversely, for the wavelengths corresponding to these atmospheric windows there will be little radiation in the atmosphere as the majority of radiation emitted by the Earth at these wavelengths is allowed to pass through the atmosphere to space.
A "selective surface" is one that exploits the atmospheric window by preferentially emitting thermal energy at wavelengths corresponding to these atmospheric windows where there is reduced incident radiation which may be absorbed by the surface, that allow rapid transfer of that radiation to space and by being non-absorptive of radiation outside these wavelengths.
SUMMARY OF THE INVENTION
The invention resides in a curable formulation for use as a radiative cooling surface coating for an external surface of a building characterised by low absorption at wavelengths of incident solar radiation and high radiative emittance at wavelengths of reduced incident radiation.
The invention is based on the discovery that such a coating may be obtained by the inclusion of a dispersion of gas or vacuum filled microspheres in a coating composition containing a solar reflective pigment. The microspheres employed are preferably of the silica type, most preferably having a shell of silica-alumina. Coatings according to the invention, incorporating effective amounts of such microspheres, have in fact demonstrated the ability to achieve below-ambient temperatures in the interior of coated structures,
The microspheres employed in such coatings may be gas filled, for example with CO2 or N or they may be vacuum filled. Preferably the coating is not only non-absorptive of solar radiation but is reflective, rather than transmissive, of these wavelengths. Preferably the coating has a solar reflectance greater than 80% and more preferably greater than 84%.
Preferably the coating is characterised by radiative emittance (ε) greater than 85 %, more preferably greater than 90% and still more preferably greater than 95% at thermal wavelengths.
The combined effect of the solar absorption and radiative emittance characteristics of the coating are such that the coating is able to absorb heat energy from within an internal air space and re-radiate that energy as thermal radiation to achieve net radiative cooling of the air space.
The coating of the invention, when applied to a sheet steel surface exposed to solar radiation at Air Mass 1.5 Solar Spectrum and ambient temperature of 20-28 °C the formulation displays a net radiative cooling effect to the air space below the steel sheet.
Preferably, the formulation of the invention is curable and may be applied to an existing building using a large area spray process.
BRIEF DESCRIPTION OF THE DRAWINGS
Preferred embodiments of the invention will now be described by way of non-limiting examples and with reference to the accompanying figures in which :-
Fig. 1 shows a graph of atmospheric absorption versus wavelength;
Fig. 2 shows the results of comparative testing of a coating according to the invention against conventional roofing systems, and
Figs. 3 to 5 show the results of further comparative testing of the invention DESCRIPTION OF PREFERRED EMBODIMENTS OF THE INVENTION
A formulation according to the invention was manufactured as follows. Quantities given are for a total 600 L mix and are provided for illustrative purposes only. Though precise quantities are stated, wide variation from these quantities, even down to zero for some components, are possible and within the scope of the invention.
610 g of a sequestrating and wetting agent, preferably a polyphosphate and 610g of a dispersing agent was added to 91 L of water in a mixing drum and mixed at 2000rpm for 10 minutes or until the ingredients are thoroughly dispersed. To this mix was added a solar reflective pigment such as rutile grade Titanium Oxide (TiO2) (38kg), 72 kg of a filler such as CaCO2 or MgCO2 that lends water resistance to the cured formulation, and 72 kg of a suspension agent e.g. MgSiO3, BaSO or SiO2 that is also abrasion and corrosion resistant on metals. The mix was then dispersed at approx 2000 rpm for 1 hour. The actual mixing times will depend on the particle size. It is preferred that mixing continues until the mixture is brought to a Hegman setting of 7 giving about 15 microns measured on a Hegman Grind Gauge.
Approx 228 L of a binder such as a styrene acrylic, acrylic resin, homopolymer or PVA was then added and mixed for 15 minutes at 1500 rpm.
Approx 3.8 L of a defoaming agent, preferably non-silicon based, was then added and mixed for 10 minutes at 1500 rpm.
1.9L of ammonia or other suitable alkali is added to adjust the pH to a range suitable for the addition of thickening agents. The ammonia was mixed for 10 minutes at 1100 rpm.
Next was added a coalescing agent such as any trimethylpentandiol, e.g. Isonol (4.8L) and mixed for 15 minutes at 1100 rpm. Propylene Glycol or other suitable glycols that act as a further coalescing agent and adjust the curing time were added and mixed for 5-10 minutes at 1100 rpm.
400 g of a non-toxic, broad range biocide was added and mixed for 5-10 minutes at 1100 rpm. The biocide may include a uni-fungicide, bactericide, insecticide and algaecide and is preferably devoid of heavy metals.
A thickening agent, preferably selected from the hydroxycellulose group (630 g) was pre-dissolved in 10 L of water and then added and mixed into the main mixture for 10- 15 minutes at 1100 rpm. The mixture thickened with the addition of this component. The viscosity was measured using a No. 4 Ford Cup and adjusted until a run through time of 35 seconds was achieved with allowances made temperature.
A plasticiser (10L), preferably phthalate, was added and mixed for 10 minutes at 1100 rpm.
The final mixing step was to add a microspheres component, in this example 70-90 kg, which was mixed for approx 30 minutes at a reduced rate of 200-300 rpm to avoid damage to the spheres. The microspheres were approximately 45 μm - 150 μm in diameter (average 50 μm is preferred) having a silica-alumina shell between 0.3 μm and 1 μm thick and a filling of CO2. The spheres form a fine light powder and are believed to enhance the emissivity of the coating at least in the wavelengths of the atmospheric windows. While CO2 -filled microspheres were used in this example, the spheres can be vacuum filled to a pressure of 4 Torr or can be filled with another gas, for example N2 .
The above ingredients other than the microspheres were chosen from those available primarily for their low solar absoφtion and high thermal emittance properties as well as for their properties that make them suitable for use as a roof coating, e.g. fire retardant, corrosion resistance, biocide etc. Those skilled in the preparation of paints and curable surface coatings will understand that the proportions of the ingredients will be adjusted to the particular application. For example, in the above formulation a relatively small quantity of white pigment (TiO ) is employed, and this can be increased where appropriate.
Coating compositions containing greater concentrations of microspheres, for example 140 Kg per 600 1, can be used to advantage. Higher concentrations, for example 150 Kg per 600 1, may also be used.
The preferred composition has at least 40% solids, more preferably at least 60% solids and still more preferably at least 70% solids.
The resultant mixture can be sealed and stored ready for application. The composition can be coated onto any exterior surface but is preferably applied to roofs that have a clear view of the sky to ensure maximum radiative cooling. A large area coating, e.g. on a warehouse roof, is best achieved by a spray coating process, for example using a Graco™ airless spray gun with Tungsten Carbide tip.
The coating may be applied as a single thick layer but will more typically be built up from a series of thin layers. The thickness at which a single layer of the coating can be applied will depend on the viscosity of the formulation and the flatness of the surface. A sloping, undulating or rough surface will require the application of thinner coats to ensure the overall coating is of even thickness across the surface.
If the coating is too thick it may act as a blanket for the building and retard the transfer of heat from the internal air space to the coating for radiative emission resulting in higher interior temperatures. It is thus preferred that the thickness of the coating is less than 10mm.
Coatings manufactured in accordance with the above example have been found by optical measurement to exhibit a hemispherical solar absorptance of 0.15, and thermal emittance estimated from measured roof heat loss coefficients is greater that 0.9. The observed radiative capability and IR spectra of the material are such, however, as to indicate the existence of selective radiative ability in the 8 to 13 μm atmospheric window.
Comparative tests have been conducted between the composition of the invention and conventional roofing systems. In the first of these test, four steel boxes, approx 330mm x 330 mm * 760mm, open at one end, were used in the tests. The boxes were inverted (i.e. open end down) so that the bottom of the box became the roof for the purpose of the test. Each box had its side walls lined with insulating batts rated at R = 1.5. Two boxes had outer surfaces of bare steel, and one of these had the underside of its roof insulated with the same batts as used on the walls. The third box was of off- white Colorbond steel, and the remaining box had the exterior side of its roof coated to a thickness of approx 0.7 mm with the composition of the invention, prepared as above.
The test boxes were disposed outside with each box having a clear view of the sky. Internal temperature readings were taken hourly for a period of 10 days. Ambient outside temperatures were also recorded. The results are graphed in Fig. 2 where the composition of the invention is referenced using the present applicant's trade mark Insulshield™. As is evident from the results, the coatings of the invention performed remarkably better than the existing roofing systems in maintaining a low temperature in the interior space of the test box and was the only product to consistently provide interior space temperatures below ambient.
It should be noted that the test period covered predominantly cloudless days and nights and that under more overcast conditions the performance of the coatings of the invention is reduced. However, even under these conditions, the coatings of the invention still out performed the prior art systems.
In a further test, an uninsulated steel enclosure was coated with a formulation of the invention, allowed to cure and then subjected to solar radiation at 1062 Wm" incident on the horizontal at ambient temperature of 23 °C with clear sky conditions. The total radiation energy off the roof of the enclosure comprised 894 Wm"2 of reflected solar energy and 188 Wm"2 of re-radiated heat (IR). The total energy output of 1082 Wm'2 was thus greater than the incident solar energy. This suggests that the coated roof was able to absorb heat energy from the air space within the enclosure and output that energy to the atmosphere.
For a similar enclosure having an insulating layer beneath the roof, the net energy output was 1064 Wm" which is less than for the uninsulated case but is still sufficient to achieve a small net cooling effect, even in conditions of high incident solar radiation.
Under clear sky night time conditions, radiative cooling continued but without the solar heat load. At 11pm, the internal temperature in the uninsulated enclosure was 16.4 °C compared with 20°C ambient and at 2 am the internal temperature was 15.7°C compared with 18.8°C ambient. In the insulated case, the internal temperatures were slightly above ambient.
From a comparison between the underside roof temperatures of an uncoated steel roof (56°C) and a similar steel roof coated according to the present invention (33°C), it can be seen that coatings of the invention when applied to roof structures can reduce the solar heat load to the internal air space due to the coating's high solar reflection properties. Because there is very little solar heating of the roof, the roof can instead absorb heat from the internal air space below the roof. The high IR emittance properties of the coating allow this absorbed heat to be efficiently radiated away from the roof, thus achieving a net cooling effect to the air space.
Furthermore, because there can be a significant temperature gradient within the air space, with the temperature just below the roof being up to several degrees higher than at the base level, this radiative cooling effect can continue to the point where ground level temperatures significantly below ambient are obtained. In a second series of tests, a field trial was conducted from December 2000 to April 2001 to evaluate the performance of the coating in a demountable classroom environment. Portable classrooms are widely used in Australia and have a reputation for overheating, particularly in the summer.
The coating of the invention is intended principally for the commercial and industrial metal-roofed buildings which generally have a much larger roof area than exterior wall surfaces area. The demountable classrooms present a "worst case scenario" in which to trial the coating for the following reasons:- low roof to wall ratio, unlike supermarkets or warehouses, sub-roof insulation, which delays internal heat reaching the coating thereby creating a time lag when compared to ambient air temperature movements, a relatively high occupancy rate of about 3m2 per person, which is about twice the density of a standard supermarket, open windows and ceiling fans that permit a high rate of external air exchange thereby increasing the difficulty for the coating to maintain internal temperatures constantly below ambient.
Despite these challenges the coating performed extraordinarily well. The maximum daily temperature of the coated room during the occupied period of the trial (February to April, 2001) was maintained at or below ambient for 84% of the time. During the unoccupied period, the coated room's peak temperature was at or below ambient 81% of the time, with differing weather conditions accounting for the variation.
Temperature recorders were located adjacent to the teacher's blackboard at a height to correctly record the temperature of the occupied portion of the room. The graphs of Figs. 5 - 6 show the results of observations in two rooms used in the test, one of which was roof-coated with the composition of the invention. (Another uncoated room contained a small window-mounted air conditioning unit, and there was no control over its use. The unit was, however, at the end of the classroom remote from the temperature sensor, and in fact the corresponding graphs for this room show that it had no appreciable affect on the measured temperature. The graphs for that room are therefore not included here). The rooms had shaded walls, while their roofs were not affected by any shading factors.
The results presented in the following graphs are taken from three periods within the trial:
Fig. 3 late December, 2000 - being the warmest period, and Fig. 4 mid April, 2001 - being the coolest period, Fig. 5 February to April, 2001 - being the occupied period and showing daily peak temperatures.
Although there were many environmental factors beyond the control of the trial including cloudy weather, air-exchange factors and room population, the coating produced excellent results over the whole period.
Reference to Fig. 3 shows that on the hottest day in December the ambient temperature reached 38°C by 12 p.m. and the unquoted class rooms peaked at 41°C by 3 p.m. However, the coated room was 8°C cooler than anibient at midday, 4°C cooler by 3 p.m. and 7°C cooler than the other rooms. Overall, it can be seen that when the ambient reached its peak on most days the coated room was generally around 6°C to 7°C below ambient. Although the temperature in the coated room reached its peak several hours later, often around 4-6 p.m., it rarely reached the maximum ambient temperature.
Also apparent from Fig. 3 is the fact that the coated room commenced cooling usually when ambient temperature fell to that of the coated room. As noted above, the time lag in the cooling of the coated room would be primarily due to the sub-roof insulation trapping internal heat which would have entered the building through air exchange or being generated from internal sources including people.
In relation to Fig. 4 a significant observation is that the coated room maintained the more even flow of temperatures, While it was considerably cooler than the other rooms as well as ambient air, it also did not get as cold overnight. At the hottest time of each day, usually around midday to 2 p.m., the coated room was about 4°C to 7°C cooler than ambient and the other rooms. April 17th is a case in point. At 10:00 a.m. the coated room is still only 18°C and ambient is 23°C. When ambient peaks at 12:00 p.m. it reaches 28°C, while the coated room is still a comfortable 22°C. The coated room eventually reached only 25.5°C around 6 p.m., long after the room was no longer in use for the day.
As ambient temperature falls in the late afternoon the insulation traps the internal heat of the now closed room and prevents it from cooling at the same rate as ambient.
Without insulation the coated building will cool at almost the same rate as the outside ambient air. This enables the design of a more economical and environmentally efficient building.
Fig. 5 shows that for 84% of the occupied period the coated room was at or below the maximum ambient temperature and almost always well below the other rooms. The days on which the coated room was slightly higher than ambient are the coolest days, when there was predominant cloud cover since the coating requires a mainly clear sky to operate. This is the ideal - in cooler or cloudy weather it is usually desirable to retain a little more internal heat.
The present applicant has found that the radiative cooling coatings of the invention are most effective when used on roofs without underlying batt insulation. It is believed that the batt insulation, while providing a barrier to the ingress of absorbed solar radiation, retards the radiative cooling mechanism by reducing the transport of heat energy from the internal air space to the coating when it can be radiated to the atmosphere.
Coatings according to the invention provide a useful alternative to conventional methods for dealing with solar heat loads. However, the suitability of their use will very much depend on the environment in which they are to be employed. The coatings will be most suitable for use on buildings where the summer time cooling costs are greater than the winter time heating costs. While the experiments to date indicate that the coatings are best used on roofs without underlying insulation, the economics of the situation may dictate that due to winter heating considerations it is best that insulation is used.
It has been found that under overcast conditions, the radiative cooling effect is reduced and it is believed that this may be because the increased levels of water vapour in the atmosphere close the atmospheric window. This is especially important at night when radiative cooling can reduce the temperature of the internal air space well below ambient. The coatings are therefore more suitable for use in less cloud dominated environments, optimally with clear sky night time conditions.
The benefits of the invention include that less reliance can be placed on air conditioning to maintain low temperatures within an air space thus leading to reduced energy consumption. This has advantages for the local system in which the invention is utilised as well as wider environmental advantages including reduced production of greenhouse gases.
The formulation of the invention may include additional components such as a biocide, fire retardant, corrosion retardant etc. or alternatively, the previously described components can be selected for these properties.
While particular embodiments of this invention have been described, it will be evident to those skilled in the art that the present invention may be embodied in other specific forms without departing from the essential characteristics thereof. The present embodiments and examples are therefore to be considered in all respects as illustrative and not restrictive, and all modifications which would be obvious to those skilled in the art are therefore intended to be embraced therein. It will further be understood that any reference herein to known prior art does not, unless the contrary indication appears, constitute an admission that such prior art is commonly known by those skilled in the art to which the invention relates.

Claims

1. A surface coating composition for the provision of a surface coating having radiative cooling properties, the composition including a solar reflective pigment and an effective quantity of microspheres.
2. A surface coating composition according to claim 1 in which the microspheres are silica microspheres.
3. A surface coating composition according to claim 2 in which the microspheres have a shell of silica-alumina.
4 A composition according to claim 1 in which the diameters of the microspheres lie substantially between 45 μm and 150 μm.
5. A composition according to claim 4 wherein the average diameter of the microspheres is approximately 50 μm.
6. A composition according to claim 3 in which the microspheres have shell thicknesses substantially between 0.3 μm and 1 μm.
7. A composition according to claim 1 containing from substantially 60 to 150 Kg of microspheres per 600 1.
8. A composition according to claim 7 containing from substantially 60 to 140 Kg of microspheres per 600 1.
9. A composition according to claim 7 containing from substantially 60 to 70 Kg of microspheres per 600 1.
10. A method of reducing the temperature within a building relative to ambient temperature, including the step of applying to the roof of the building a coating containing a solar reflective pigment and an effective quantity of microspheres.
11. A building having a roof substantially exposed to the sky, the roof having a surface coating containing a solar reflective pigment and an effective quantity of microspheres.
12. A surface coating composition substantially as described herein.
PCT/AU2002/000695 2001-06-07 2002-06-03 Radiative cooling surface coatings WO2002098996A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP02729636A EP1409596A4 (en) 2001-06-07 2002-06-03 Radiative cooling surface coatings
AU2002302177A AU2002302177B2 (en) 2001-06-07 2002-06-03 Radiative cooling surface coatings
CN028126017A CN1518582B (en) 2001-06-07 2002-06-03 Radiative cooling surface coatings
JP2003502108A JP2004532919A (en) 2001-06-07 2002-06-03 Radiant cooling surface coating
US10/479,835 US7503971B2 (en) 2001-06-07 2002-06-03 Radiative cooling surface coatings
ZA2004/02724A ZA200402724B (en) 2001-06-07 2004-04-07 Radiative cooling surface coatings

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPR5545A AUPR554501A0 (en) 2001-06-07 2001-06-07 Radiative cooling surface coatings
AUPR5545 2001-06-07

Publications (2)

Publication Number Publication Date
WO2002098996A1 true WO2002098996A1 (en) 2002-12-12
WO2002098996B1 WO2002098996B1 (en) 2003-01-09

Family

ID=3829519

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2002/000695 WO2002098996A1 (en) 2001-06-07 2002-06-03 Radiative cooling surface coatings

Country Status (8)

Country Link
US (1) US7503971B2 (en)
EP (1) EP1409596A4 (en)
JP (1) JP2004532919A (en)
CN (1) CN1518582B (en)
AU (2) AUPR554501A0 (en)
IN (1) IN2004DE00034A (en)
WO (1) WO2002098996A1 (en)
ZA (1) ZA200402724B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007034248A1 (en) * 2005-09-23 2007-03-29 Zdenko Simic Overhead conductor with spectrally selective surface
WO2008154694A1 (en) * 2007-06-19 2008-12-24 University Of Technology, Sydney A cooling material using particles arranged for generation of surface plasmon resonances
WO2008154691A1 (en) * 2007-06-19 2008-12-24 University Of Technology, Sydney A cooling material
CN102002312A (en) * 2010-11-22 2011-04-06 东南大学 Temperature-controlled solar radiation permeable energy-saving window coating film
WO2017066795A3 (en) * 2015-10-16 2017-05-18 Stc. Unm Microsphere-based coatings for radiative cooling under direct sunlight
WO2023192807A1 (en) * 2022-03-28 2023-10-05 Ts Conductor Corp. Composite conductors including radiative and/or hard coatings and methods of manufacture thereof

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4932179B2 (en) * 2004-07-02 2012-05-16 新日本製鐵株式会社 Exterior wall structure, roof structure
US7451055B2 (en) * 2007-04-02 2008-11-11 Intellicoat Technologies, Inc. Method and system for measuring energy savings resultant from improvements made to a structure
FR2917417B1 (en) * 2007-06-13 2012-08-31 Commissariat Energie Atomique USE OF A COMPOSITION COMPRISING A POLYMERIC MATRIX FOR NATURAL RADIATION COOLING AND WATER VAPOR CONDENSATION.
US9631367B2 (en) 2011-08-05 2017-04-25 Certainteed Corporation System, method and apparatus for increasing surface solar reflectance of roofing
US10315385B2 (en) 2011-08-05 2019-06-11 Certainteed Corporation System, method and apparatus for increasing surface solar reflectance of roofing
US9859038B2 (en) 2012-08-10 2018-01-02 General Cable Technologies Corporation Surface modified overhead conductor
US9709349B2 (en) * 2012-11-15 2017-07-18 The Board Of Trustees Of The Leland Stanford Junior University Structures for radiative cooling
US10957468B2 (en) 2013-02-26 2021-03-23 General Cable Technologies Corporation Coated overhead conductors and methods
US9923111B2 (en) 2013-11-13 2018-03-20 The Board Of Trustees Of The Leland Stanford Junior University Illumination and radiative cooling
US10088251B2 (en) 2014-05-21 2018-10-02 The Board Of Trustees Of The Leland Stanford Junior University Radiative cooling with solar spectrum reflection
AU2015274619B2 (en) 2014-06-10 2019-02-14 General Cable Technologies Corporation Curable two-part coatings for conductors
CN104530880A (en) * 2014-12-15 2015-04-22 唐云 Intelligent temperature-regulating energy-saving type emulsion paint for exterior wall
US20170350663A1 (en) * 2015-06-03 2017-12-07 Pc Krause And Associates, Inc. Composite material for passive radiative cooling
US11440291B2 (en) * 2015-06-03 2022-09-13 PC Krause and Associates Composite material for passive radiative cooling
EP3311094A4 (en) 2015-06-18 2019-04-10 The Trustees of Columbia University in the City of New York Systems and methods for radiative cooling and heating
EP3326176A4 (en) 2015-07-21 2019-01-23 General Cable Technologies Corporation Electrical accessories for power transmission systems and methods for preparing such electrical accessories
EP3420024A4 (en) * 2016-02-23 2020-02-19 Advanced Environmental Recycling Technologies, Inc Compositions and methods for reducing the surface temperature of composite articles
EP3423298B1 (en) 2016-02-29 2021-07-28 The Regents of the University of Colorado, a body corporate Selective radiative cooling structure
US10502505B2 (en) 2016-02-29 2019-12-10 The Regents of the Univeristy of Colorado, a body corporate Radiative cooling structures and systems
US10323151B2 (en) 2017-02-27 2019-06-18 Palo Alto Research Center Incorporated Coating to cool a surface by passive radiative cooling
WO2019191690A1 (en) 2018-03-29 2019-10-03 The Board Of Trustees Of The Leland Stanford Junior University Apparatuses and methods involving thermally tuned composite material
WO2020140082A1 (en) 2018-12-27 2020-07-02 SkyCool Systems, Inc. Cooling panel system
EP3956614A1 (en) 2019-04-17 2022-02-23 Skycool Systems, Inc. Radiative cooling systems
CN110317521A (en) * 2019-07-05 2019-10-11 宁波瑞凌新能源科技有限公司 Selective radiation refrigeration coating and its composite material and methods for using them
US11874073B2 (en) 2020-04-09 2024-01-16 The Hong Kong University Of Science And Technology Radiative cooling structure with enhanced selective infrared emission
CN113845776B (en) * 2020-06-28 2022-11-11 中国科学院上海硅酸盐研究所 Polydimethylsiloxane and silicon dioxide microsphere composite thick film and preparation method thereof
CN111995895B (en) * 2020-08-31 2021-09-21 宁波瑞凌新能源科技有限公司 Particulate material and use thereof
WO2023057998A1 (en) 2021-10-08 2023-04-13 Tata Steel Limited A coating composition, process of obtaining the composition and methods thereof
CN114231073A (en) * 2021-12-20 2022-03-25 佛山纳诺特科技有限公司 Core-shell structure reflective substrate, daytime radiation refrigeration coating, coating and preparation method
CN115785809B (en) * 2022-12-07 2023-06-06 科顺防水科技股份有限公司 Radiation refrigeration coating and radiation refrigeration product
CN116716039B (en) * 2023-08-11 2023-12-26 北京助天科技集团有限公司 Photocatalytic radiation refrigeration coating, preparation method and application
CN117567878B (en) * 2024-01-11 2024-04-05 中稀易涂科技发展有限公司 High-performance porous radiation refrigeration filler and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2326634A (en) * 1941-12-26 1943-08-10 Minnesota Mining & Mfg Reflex light reflector
US3228897A (en) * 1961-10-26 1966-01-11 Minnesota Mining & Mfg Reflective coating compositions containing glass beads, metal flake pigment and binder
US5713974A (en) * 1994-09-06 1998-02-03 Thermacell Technologies, Inc. Insulation microspheres and method of manufacture
US5750191A (en) * 1994-05-20 1998-05-12 Minnesota Mining And Manufacturing Company Retroreflective elements
US5774265A (en) * 1996-02-05 1998-06-30 Minnesota Mining And Manufacturing Company Durable retroreflective elements
US6214450B1 (en) * 1998-02-25 2001-04-10 Tremco Incorporated High solids water-borne surface coating containing hollow particulates

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3043112A (en) * 1959-02-09 1962-07-10 Commw Scient Ind Res Org Method and means for producing refrigeration by selective radiation
FR82838E (en) * 1962-12-27 1964-04-24 Centre Nat Rech Scient Device for lowering the temperature of a body by its own radiation and application to the production of cold
FR2346403A1 (en) * 1975-10-31 1977-10-28 Inst Francais Du Petrole IMPROVED LIGHTNESS RESINS AND THEIR PREPARATION
GB2099444B (en) * 1981-05-29 1984-08-01 Berger Jenson & Nicholson Ltd Anti-fouling compositions
JPH072926B2 (en) 1984-02-24 1995-01-18 日本ペイント株式会社 Building exterior coating composition
US5786785A (en) * 1984-05-21 1998-07-28 Spectro Dynamics Systems, L.P. Electromagnetic radiation absorptive coating composition containing metal coated microspheres
US4624113A (en) * 1985-06-27 1986-11-25 The United States Of America As Represented By The United States Department Of Energy Passive-solar directional-radiating cooling system
JPH02150475A (en) 1988-11-30 1990-06-08 Chuo Rika Kogyo Kk Coating composition having moisture-permeability, elongation and water-proofing property
US5006175A (en) * 1990-02-27 1991-04-09 Engelhard Corporation High infra red reflecting brown rutile pigment compositions
US5310422A (en) * 1992-12-01 1994-05-10 General Electric Co. High temperature inorganic paint
US5415950A (en) * 1993-11-08 1995-05-16 E. I. Du Pont De Nemours And Company Holographic flake pigment
DE4418214C2 (en) * 1994-05-25 1999-02-04 Gerd Hugo Paint with low emissivity in the area of thermal radiation
US20010044489A1 (en) * 1994-05-25 2001-11-22 Gerd Hugo Coating substance with low emissivity in the heat radiation range
US5811180A (en) * 1994-07-26 1998-09-22 The Regents Of The University Of California Pigments which reflect infrared radiation from fire
JP3794824B2 (en) * 1998-05-13 2006-07-12 長島特殊塗料株式会社 Thermal barrier paint
US6174360B1 (en) * 1998-10-26 2001-01-16 Ferro Corporation Infrared reflective color pigment
JP3794837B2 (en) * 1998-10-27 2006-07-12 長島特殊塗料株式会社 Thermal barrier paint and coating method thereof
JP2000126678A (en) * 1998-10-27 2000-05-09 Nagashima Tokushu Toryo Kk Coated metallic sheet coated with heat shieldable coating material
JP4138129B2 (en) * 1999-01-26 2008-08-20 勝夫 三木 Solar heat shielding paint
JP2000327740A (en) 1999-03-12 2000-11-28 Toray Thiokol Co Ltd Curable composition
JP2000281894A (en) 1999-04-01 2000-10-10 Toray Thiokol Co Ltd Curable composition
JP2001064544A (en) 1999-08-25 2001-03-13 Asahi Glass Co Ltd Heat-insulation coating film
JP2002060698A (en) * 2000-08-15 2002-02-26 Origin Electric Co Ltd Infrared transmitting layer-forming composition, infrared reflector and treated matter
DE10044216A1 (en) * 2000-09-07 2002-05-02 Fraunhofer Ges Forschung Coating material for multifunctional, superphobic layers
DE10102789A1 (en) * 2001-01-22 2002-08-01 Gerd Hugo Coating with low solar absorption
US6875800B2 (en) * 2001-06-18 2005-04-05 Ppg Industries Ohio, Inc. Use of nanoparticulate organic pigments in paints and coatings

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2326634A (en) * 1941-12-26 1943-08-10 Minnesota Mining & Mfg Reflex light reflector
US3228897A (en) * 1961-10-26 1966-01-11 Minnesota Mining & Mfg Reflective coating compositions containing glass beads, metal flake pigment and binder
US5750191A (en) * 1994-05-20 1998-05-12 Minnesota Mining And Manufacturing Company Retroreflective elements
US5713974A (en) * 1994-09-06 1998-02-03 Thermacell Technologies, Inc. Insulation microspheres and method of manufacture
US5774265A (en) * 1996-02-05 1998-06-30 Minnesota Mining And Manufacturing Company Durable retroreflective elements
US6214450B1 (en) * 1998-02-25 2001-04-10 Tremco Incorporated High solids water-borne surface coating containing hollow particulates

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
See also references of EP1409596A4
TAZAWA: "IR properties ofSiO deposited on V1x Wx 02 thermochromic films by vacuum evaporation", THIN SOLID FILMS, vol. 375, 2000, pages 100 - 103

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007034248A1 (en) * 2005-09-23 2007-03-29 Zdenko Simic Overhead conductor with spectrally selective surface
WO2008154694A1 (en) * 2007-06-19 2008-12-24 University Of Technology, Sydney A cooling material using particles arranged for generation of surface plasmon resonances
WO2008154691A1 (en) * 2007-06-19 2008-12-24 University Of Technology, Sydney A cooling material
CN102002312A (en) * 2010-11-22 2011-04-06 东南大学 Temperature-controlled solar radiation permeable energy-saving window coating film
WO2017066795A3 (en) * 2015-10-16 2017-05-18 Stc. Unm Microsphere-based coatings for radiative cooling under direct sunlight
US10514215B2 (en) 2015-10-16 2019-12-24 Stc. Unm Microsphere-based coatings for radioactive cooling under direct sunlight
WO2023192807A1 (en) * 2022-03-28 2023-10-05 Ts Conductor Corp. Composite conductors including radiative and/or hard coatings and methods of manufacture thereof
US11854721B2 (en) 2022-03-28 2023-12-26 Ts Conductor Corp. Composite conductors including radiative and/or hard coatings and methods of manufacture thereof

Also Published As

Publication number Publication date
JP2004532919A (en) 2004-10-28
US7503971B2 (en) 2009-03-17
AUPR554501A0 (en) 2001-07-12
AU2002302177A1 (en) 2002-12-16
EP1409596A4 (en) 2004-09-01
IN2004DE00034A (en) 2006-02-24
EP1409596A1 (en) 2004-04-21
ZA200402724B (en) 2005-06-29
CN1518582B (en) 2012-09-26
CN1518582A (en) 2004-08-04
AU2002302177B2 (en) 2007-12-06
WO2002098996B1 (en) 2003-01-09
US20050064094A1 (en) 2005-03-24

Similar Documents

Publication Publication Date Title
US7503971B2 (en) Radiative cooling surface coatings
JP7023978B2 (en) Radiative cooling function paint and its applications
Berdahl et al. Preliminary survey of the solar reflectance of cool roofing materials
US9371665B2 (en) Article of the tent or shelter type
Song et al. Optical properties across the solar spectrum and indoor thermal performance of cool white coatings for building energy efficiency
US5811180A (en) Pigments which reflect infrared radiation from fire
Yang et al. Passive daytime radiative cooling: Principle, application, and economic analysis
Vox et al. Evaluation of the radiometric properties of roofing materials for livestock buildings and their effect on the surface temperature
US10000663B1 (en) Protective flowable or spreadable composition, articles of manufacture, an apparatus for manufacture and a process for manufacture thereof
US20220381524A1 (en) Systems and Methods for Spectrally Selective Thermal Radiators with Partial Exposures to Both the Sky and the Terrestrial Environment
US6902611B2 (en) Heat dissipating coating and method for decreasing the inner temperature of buildings and similar constructions
JPS6086173A (en) Solar heat reflective coating composition having radiational cooling function
EP3006513B1 (en) Heat-reflective composition
US7566493B2 (en) Coating composition
US20130323500A1 (en) Flaked borosilicate glass coatings
CN101560343B (en) Heat-reflecting heat-insulating inorganic material, preparation method and application thereof
US20230416537A1 (en) Colorful Low-Emissivity Paints for Space Heating and Cooling Energy Efficiency
Joseph et al. Subambient passive radiative cooling effects of barium sulfate and calcium carbonate paints under Malaysia's tropical climate
CN108424696A (en) A kind of water-and acrylate water-proof heat-insulating paint and preparation method thereof
Yang et al. A comprehensive investigation of zeolite/polyurea cooling coating on concrete for building energy conservation
Hugo Effects of low emissive wall coatings on thermal comfort and energy consumption
EA008025B1 (en) Composite decorative-protection coating
Bell et al. Advanced Roof Coatings: Materials and their Applications
CN115216185A (en) Reflective heat-insulation coating, preparation method thereof and reflective heat-insulation composite layer
JAWORSKI NANO-INSULATING vs LEED

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

AK Designated states

Kind code of ref document: B1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: B1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

B Later publication of amended claims
121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2003502108

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 028126017

Country of ref document: CN

WWE Wipo information: entry into national phase

Ref document number: 2002302177

Country of ref document: AU

Ref document number: 2002729636

Country of ref document: EP

Ref document number: 34/DELNP/2004

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2004/02724

Country of ref document: ZA

Ref document number: 200402724

Country of ref document: ZA

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 2002729636

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 10479835

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 1-2004-500028

Country of ref document: PH