Geopolymer-based sub-ambient daytime radiative cooling coating

Abstract

Sub-ambient daytime radiative cooling (SDRC) coating comprising: an alkali activated metakaolin, BaSO.sub.4, and silica nanospheres, wherein the alkali activated metakaolin is prepared by reaction of metakaolin with an alkali activator comprising waterglass and a strong base selected from the group consisting of LiOH, NaOH, KOH, Ca(OH).sub.2, Li.sub.2O Na.sub.2O, K.sub.2O, CaO, and a mixture thereof, a coating formulation comprising the same, and a method of preparation and use thereof.

Claims

1. A sub-ambient daytime radiative cooling (SDRC) coating composition comprising: an alkali activated metakaolin, BaSO.sub.4, and silica nanospheres, wherein the alkali activated metakaolin is prepared by reaction of metakaolin with an alkali activator, wherein the alkali activator comprises waterglass and a strong base selected from the group consisting of LiOH, NaOH, KOH, Ca(OH).sub.2, Li.sub.2O Na.sub.2O, K.sub.2O, CaO, and a mixture thereof.

2. The SDRC coating composition of claim 1, wherein the SDRC has a solar reflectance of 0.9667-0.9758 between 100-2,500 nm.

3. The SDRC coating composition of claim 1, wherein the SDRC has an infrared emissivity of 0.90-0.9491 between 8-13 m.

4. The SDRC coating composition of claim 1, wherein the BaSO.sub.4 is present in the coating composition at 50-70 wt %.

5. The SDRC coating composition of claim 1, wherein the BaSO.sub.4 is present in the coating composition at 60-63 wt %.

6. The SDRC coating composition of claim 1, wherein the silica nanospheres have an average diameter between 10-100 nm.

7. The SDRC coating composition of claim 1, wherein the silica nanospheres have an average diameter between 20-50 nm.

8. The SDRC coating composition of claim 1, wherein the silica nanospheres are present in the coating composition at 0.5-2.0 wt %.

9. The SDRC coating composition of claim 1, wherein the silica nanospheres are present in the coating composition at 1.5-2.0 wt %.

10. The SDRC coating composition of claim 1, wherein the BaSO.sub.4 is present in the coating composition at 60-63 wt % and the silica nanospheres are present in the coating composition at 1.5-2.0 wt %.

11. The SDRC coating composition of claim 1, wherein the alkali activator comprises waterglass comprising sodium silicate and NaOH.

12. The SDRC coating composition of claim 11, wherein the waterglass has a modulus of 1-5.

13. The SDRC coating composition of claim 12, wherein the metakaolin and the alkali activator are combined in a mass ratio of metakaolin to a solid content of the alkali activator of 1:1 to 1.2:1, respectively.

14. The SDRC coating composition of claim 1, further comprising one or more additives selected from the group consisting of polytetrafluoroethylene, Ca(OH).sub.2, MgF.sub.2, BaTiO.sub.3, light-weight lime, and ground lime.

15. The SDRC coating composition of claim 2, wherein the alkali activator comprises waterglass comprising sodium silicate and NaOH, the waterglass has a modulus of 3-3.5, the metakaolin and the alkali activator are combined in a mass ratio of metakaolin to a solid content of the alkali activator of 1:1 to 1.1:1, respectively; the BaSO.sub.4 is present in the coating composition at 60-63 wt %; the silica nanospheres have an average diameter between 20-50 nm; the silica nanospheres are present in the coating composition at 1.5-2.0 wt %; and the SDRC has an infrared emissivity of 0.93-0.9491 between 8-13 m.

16. A sub-ambient daytime radiative cooling (SDRC) coating formulation comprising the SDRC coating composition of claim 1 and water.

17. A method of applying the SDRC coating formulation of claim 16 to a surface of a substrate, the method comprising: applying the SDRC coating formulation to the surface of the substrate thereby forming a SDRC coating on the surface of the substrate; and removing at least a portion of the water from the SDRC coating.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The above and other objects and features of the present disclosure will become apparent from the following description of the disclosure, when taken in conjunction with the accompanying drawings.

(2) FIG. 1 depicts a schematic cooling mechanism of the geopolymer cooling coating.

(3) FIG. 2 depicts the optical properties of SDRC coating samples with different functional fillers. (a) Solar reflectance of AAGP matrix and AAGP coatings with different fillers. (b, c) Solar reflectance of AAGP coatings with varied addition ratio of BaSO.sub.4 (b) and further modification of SiO.sub.2 (c). (d) Infrared emissivity of the optimized AAGP cooling coating.

(4) FIG. 3 depicts XRD of the raw materials (a) and AAGP coatings with different fillers (b). FTIR of the raw materials (c), AAGP matrix and AAGP coatings with different fillers (d).

(5) FIG. 4 depicts SEM micrographs of metakaolin (a), SiO.sub.2 (b), BaSO.sub.4 (c), PTFE (d), and AAGP coatings under 2000 magnification (e) and 10000 magnification (f).

(6) FIG. 5 depicts SEM image (a), SEM image (b) and elemental mapping (c) of section of the AAGP coating.

(7) FIG. 6 depicts cooling performance of an (a) AAGP-coated board in comparison to an (b) uncoated board and the ambient temperature.

(8) FIG. 7 Schematics and photos of the test setup for AAGP coating.

(9) FIG. 8 The AAGP coating before and after the mechanical linear abrasion test: thickness reduction (a), solar reflectance (b) and SEM of the surface morphology of the coating before abrasion (c) and after abrasion (d).

(10) FIG. 9 Results of pull-out bond test (a), photos of the dolly used in the pull-out test (b) and photo of the water permeation test (c).

(11) FIG. 10 TG-DTA thermograms of AAGP matrix (a) and AAGP coating (d) with different fillers (b and c) subjected to elevated temperature (from 30 to 1000 C.).

DETAILED DESCRIPTION

Definitions

(12) Throughout the application, where compositions are described as having, including, or comprising specific components, or where processes are described as having, including, or comprising specific process steps, it is contemplated that compositions of the present teachings can also consist essentially of, or consist of, the recited components, and that the processes of the present teachings can also consist essentially of, or consist of, the recited process steps.

(13) In the application, where an element or component is said to be included in and/or selected from a list of recited elements or components, it should be understood that the element or component can be any one of the recited elements or components, or the element or component can be selected from a group consisting of two or more of the recited elements or components. Further, it should be understood that elements and/or features of a composition or a method described herein can be combined in a variety of ways without departing from the spirit and scope of the present teachings, whether explicit or implicit herein.

(14) It should be understood that the order of steps or order for performing certain actions is immaterial so long as the present teachings remain operable. Moreover, two or more steps or actions may be conducted simultaneously.

(15) The use of the singular herein includes the plural (and vice versa) unless specifically stated otherwise. In addition, where the use of the term about is before a quantitative value, the present teachings also include the specific quantitative value itself, unless specifically stated otherwise. As used herein, the term about refers to a 10%, 7%, 5%, 3%, 1%, or 0% variation from the nominal value unless otherwise indicated or inferred.

(16) Provided herein is a SDRC coating useful for sub-ambient radiative cooling. The SDRC coating can comprise: an alkali activated metakaolin, BaSO.sub.4, and silica nanospheres, wherein the alkali activated metakaolin is prepared by reaction of metakaolin with SiO.sub.2 and M.sub.2O, wherein M for each instance is independently Li, Na, or K.

(17) Metakaolin (Al.sub.2Si.sub.2O.sub.7) is a dehydration product of kaolinite (Al.sub.2(OH).sub.4Si.sub.2O.sub.5), which can be produced by calcination of kaolinite.

(18) Alkali activation of metakaolin involves the alkaline hydrolysis and dissolution of metakaolin and formation of a complex mixture of monomeric, dimeric, oligomeric oxide species, nucleation of the complex mixture and reprecipitation of aluminosilicate species.

(19) Alkali activation of metakaolin can be accomplished by reacting metakaolin with an alkali activator comprising waterglass and a strong base, such as LiOH, NaOH, KOH, Ca(OH).sub.2, Li.sub.2O Na.sub.2O, K.sub.2O, CaO, or a mixture thereof. In certain embodiments, alkali activation of metakaolin is accomplished by reacting metakaolin with an alkali activator comprising waterglass and M.sub.2O or MOH, wherein M for each instance is independently Li, Na, or K and the waterglass comprises one or more metal silicate comprising a cation selected from the group consisting of Li, Na, K, and Ca. In certain embodiments, MOH is NaOH. In certain embodiments, metakaolin is activated by reaction with an alkali activator comprising waterglass comprising sodium silicate and NaOH in water.

(20) Waterglass as used herein, can refer to an aqueous solution comprising one or more metal silicates selected from the group consisting of lithium silicate, sodium silicate, potassium silicate, calcium silicate, and mixtures thereof. In certain embodiments, waterglass comprises sodium silicate. Waterglass is available commercially or can be prepared directly by combining one or more metal silicates with water.

(21) Waterglass can have a modulus value between 1-5, 2-5, 2.5-5, 3-5, 3-4.5, 3-4, 3-3.5, 1.5-4.5, 1.5-4, 1.5-3.5, 2-3.5, or 2.5-3.5. In certain embodiments, the modulus value of the waterglass is about 3.2.

(22) The solid content of the waterglass can range from 20-50%, 20-40%, or 30-40%. In certain embodiments, the waterglass has a solid content of about 34.2%.

(23) The alkali activator can have a solid content of 10-70%, 10-60%, 10-50%, 10-40%, 20-50%, 20-40%, 30-40%, 35-40%, 20-60%, 30-50%, 35-45%, or 40-45%. In certain embodiments, the alkali activator has a solid content of about 38.5% or about 40.7%.

(24) The alkali activator can have a modulus value between 1-4, 1-3.5, 1-3, 1-2.5, 1-2, or 1-1.15. In certain embodiments, the alkali activator has a modulus value of about 1.23.

(25) The mass ratio of the solid content of the alkali activator to metakaolin can range from 10:1 to 1:10, 5:1 to 1:5, 4:1 to 1:4, 3:1 to 1:3, 2:1 to 1:2, 3:2 to 1:2, 3:2 to 2:3, 4:5 to 5:4, or 11:10 to 10:11, respectively. In certain embodiments, the mass ratio of the solid content of the alkali activator to the metakaolin is about 77 to about 80, respectively.

(26) The SDRC coating can comprise BaSO.sub.4 at a concentration of 50-70 wt %, 60-70 wt %, 63-70 wt %, or 60-63 wt %. In certain embodiments, the SDRC coating comprises BaSO.sub.4 at a concentration of about 60 wt %.

(27) The SDRC coating can comprise the silica nanospheres at a concentration of 0.5-2.5 wt %, 1.0-2.5 wt %, 1.5-2.5 wt %, 2.0-2.5 wt %, 0.5-2.0 wt %, 0.5-1.5 wt %, 1.0-1.5 wt %, or 1.5-2.0 wt %. In certain embodiments, the SDRC coating comprises the silica nanospheres at a concentration of about 1.5 wt %.

(28) The silica nanospheres can have an average diameter of 10-300 nm, 10-250 nm, nm, 10-150 nm, 10-100 nm, 10-90 nm, 10-80 nm, 10-70 nm, 10-60 nm, 10-50 nm, 20-50 nm, 20-40 nm, or 25-35 nm. In certain embodiments, the silica nanospheres have an average diameter of about 30 nm. In certain embodiments, the silica nanospheres are monodisperse.

(29) The SDRC coating can optionally comprise one or more additives selected from the group consisting of polytetrafluoroethylene, Ca(OH).sub.2, MgF.sub.2, BaTiO.sub.3, light-weight lime, and ground lime. The one or more additives can be present in the SDRC coating at a concentration between 1-10 wt %, 1-9 wt %, 1-8 wt %, 1-7 wt %, 1-6 wt %, 1-5 wt %, 1-4 wt %, 1-3 wt %, 1-2 wt %, 2-10 wt %, 3-10 wt %, 4-10 wt %, 5-10 wt %, 6-10 wt %, 5-10 wt %, 6-10 wt %, 7-10 wt %, 8-10 wt %, 9-10 wt %, 2-9 wt %, 3-8 wt %, 4-6 wt %, 4-5 wt %, or 5-6 wt %.

(30) The SDRC coating may be applied to a surface of a substrate by deposition of a SDRC coating formulation comprising the SDRC coating and water. The SDRC coating formulation may be a suspension, emulsion, or mixture. The SDRC coating formulation may comprise up to 40%, up to 35%, up to 30%, up to 25%, up to 20%, up to 15%, up to 10%, or up to 5% by weight water. In certain embodiments, the SDRC coating formulation comprises 5-40%, 10-40%, 15-40%, 20-40%, 20-35%, 25-35%, or 25-30% by weight water.

(31) The SDRC coating can exhibit a solar reflectance of 0.9667-0.9758, 0.9633-0.9758, 0.9719-0.9758, or 0.9722-0.9758, between 100-2,500 nm. In certain embodiments, the SDRC coating exhibits a solar reflectance of about 0.9758.

(32) The SDRC coating can exhibit an infrared emissivity of 0.90-0.9491, 0.91-0.9491, 0.93-0.9491, or 0.95-0.9491 between 8-13 m. In certain embodiments, the SDRC exhibits an infrared emissivity of about 0.9491.

(33) The present disclosure also provides a method of applying the SDRC coating formulation to a surface of a substrate, the method comprising: applying the SDRC coating formulation to the surface of the substrate thereby forming a SDRC coating on the surface of the substrate; and removing at least a portion of the water from the SDRC coating thereby causing the SDRC coating to harden.

(34) The SDRC coating formulation can be applied to a wide variety of surfaces such as, for example, the surface of substrates composed of paper, wood, concrete, cement, asphalt, metal (e.g., streel, aluminum alloy, etc), glass, gypsum, ceramic, ceramic tiles, plastic, plaster, masonry, resin, and roofing substrates such as asphaltic coatings, roofing felts, foamed polyurethane insulation; or to previously painted, primed, undercoated, worn, or weathered substrates. In certain embodiments, the SDRC coating formulation is applied to the exterior walls and/or roof of a commercial, industrial, or residential building.

(35) The SDRC coating can further comprise a water-proof layer disposed on a surface of the SDRC coating, which can enhance the water-resistance of the coated SDRC coating. In certain embodiments, the water-proof layer comprises a silane coupling agent, such as -aminopropyltriethoxy silane, -epoxypropyl triethoxyl silane, -glycidoxy butyl trimethoxy silane, glycidyl oxy methyl triethoxyl silane, and mixtures thereof.

EXPERIMENTAL

Materials

(36) The inorganic geopolymer coating was made from metakaolin (i.e., the precursor material) and alkali activator solution (AA) which was prepared by mixing water, sodium hydroxide, and waterglass (with modulus 3.2 and solid content of 34.2%). The Venator BLANC FIXE N-type nano-precipitated barium sulphate (BaSO.sub.4, 1 m) and monodispersed silica nanosphere (nano-SiO.sub.2, 99.5%, 305 nm) were used to improve the reflectance and infrared emission. Polytetrafluoroethylene (PTFE DISP 33, fluoropolymer resin) was used as a lubricant additive to improve the film formability and calcium hydroxide powder (Ca(OH).sub.2) in analytical grade was used to increase the early strength under ambient curing. Magnesium fluoride (MgF.sub.2, AR, 3 m, Sinopharm Chemical Reagent Co. Ltd.); barium titanite (BaTiO.sub.3, AR, 200 nm RHAWN Chemical Co. Ltd.); light-weight lime (light calcium carbonate, CaCO.sub.3, AR, 1 m, Xilong Scientific Co., Ltd) and ground lime (heavy calcium carbonate, CaCO.sub.3, AR, 2 m, Tianjin Kemiou Chemical Reagent Co., Ltd.) were selected for optical performance comparison. The modified silane coupling agent (KH-800, Hangzhou Jessica Chemical Co. Ltd.) was used for hydrophobic treatment of the developed coating for improving the waterproofing property and durability.

Example 1Synthesis of Geopolymer Coating

(37) The alkali activator (AA) was prepared with the molar ratio (i.e., SiO.sub.2/Na.sub.2O) of 1.2 and solid content of 38.5%. 50 g AA was firstly added to a beaker, and then 20 g MK and about 25 g zirconium grinding beads were added into the beaker for mixing and stirring. During the stirring process, 20 g water, 3 g SiO.sub.2, 70 g BaSO.sub.4 and 10 g PTFE emulsion were added in order. The mixture was then stirred at 1200 rpm for 20 minutes. Afterwards, 1.5 g Ca(OH).sub.2 was added into the beaker with stirring for 2 min. The final product, alkali activated geopolymer (AAGP) slurry was then obtained by removing the zirconium grinding beads through filtering. The coating was then sprayed onto a standard fiber cement board substrate with the dimensions of 300 mm300 mm4 mm, (GB/T 9271-2008) using a spray gun with pressure of 5 MPa for about 50 s and the operation was repeated in approximately 3 min. The thickness of the above coating film after drying was at 50050 m as measured by a micrometers thickness gauge. Finally, the sample surface was treated with silane coupling agent KH-800 solution (diluted to 20% in ethanol) for hydrophobic treatment before field tests and durability tests.

Example 2Optical Measurements

(38) The solar absorbance, reflectance, and transmittance of the developed AAGP coatings were measured in accordance with ASTM E903-12, for which a PerkinElmer Lambda 1050+UV/VIS/NIR Wide Band Spectrometer equipped with an integral sphere was employed. The infrared emissivity of AAGP coatings was measured using a FTIR spectrometer (Vertex 70, Bruker).

Example 3Material Characterization

(39) To analyze the physicochemical properties of both raw materials (i.e., metakaolin, BaSO.sub.4, nano silica, PTFE and Ca(OH).sub.2) and the formed AAGP coatings (i.e., with different fillers), XRD and FTIR analysis were conducted. XRD tests were performed to figure out the materials' crystallographic structures on a Bruker D8 ADVANCE A25X X-ray Diffractometer (Bruker AXS Ltd., Germany); FTIR spectroscopy was tested on a Thermo Fisher Nicolet iS10 FTIR spectrophotometer (Thermo Fisher, Germany) to analyze the functional groups and corresponding characteristic peaks. To further identify the microstructural properties and elemental distributions in the AAGP cooling coating, SEM and EDS were examined using TESCAN VEGA3 (TESCAN ORSAY HOLDING, Kohoutovice, Brno). It should be noted that only the optical tests were conducted for all the formed AAGP coatings while the other above-mentioned material characterization tests were conducted only for the AAGP coatings with the optimal contents of BaSO.sub.4 and SiO.sub.2 (which were respectively determined as 60 wt % and 1.5 wt % based on the prior optical tests as discussed in the latter sessions).

Example 4Field Test

(40) To evaluate the cooling performance, the AAGP cooling coating was prepared on a standard fiber-reinforced cement board and then hydrophobically treated with silane coupling agent KH-800 for long-lasting maintenance of optimal properties. The real-time surface temperatures of uncoated board and AAGP coated boards were recorded using a multichannel temperature collector (MEMORY HiLOGGER LR8431-30, HIOKI, E. E. Co. Ltd.). Thermocouple wires, KPS-TT-K-24-SLE-100 were purchased from Tianjin KAIPUSEN Heating & Cooling Equipment Co., Ltd. A mini weather station (Beijing Top Flag Technology Co., Ltd.) was installed for air temperature and humidity data collection.

Example 5Durability Test

(41) The linear abrasion test of AAGP coatings was carried out on standard sandpaper (320 mesh) with a 500 g abrading load to compare the solar reflectance performance and microscopic appearance of the coating surface before and after the abrasion. The water permeability test of AAGP coating was carried out according to standard of Japan Society of Civil Engineers JSCE-K571-2004. The pull-off tests of AAGP coatings were carried out with specially designed equipment (PosiTest AT-M Adhesion Tester) according to ASTM D4541. The size of the dolly used was 20 mm in diameter. All the above tests were carried out at room temperature. To determine the thermal stability and compositions of AAGP coating with different fillers, TGA tests were conducted on a Rigaku Thermo Plus EVO2 Thermalgravimetry Analyser.

Example 6Optical Performance

(42) In order to achieve high radiative cooling performance and daytime sub-ambient cooling, the coating needs to meet two conditions as follows: (1) minimizing the absorption from the solar spectrum (high solar reflectance). (2) maximizing the emissivity at the atmospheric window (high emittance in the wavelength of 8 to 13 m).

(43) Similar to the previously reported strategies for boosting the solar reflectance and infrared emissivity of a polymeric coating, nano-sized functional fillers were utilized to modify the optical performance of AAGP coating. Nano-SiO.sub.2 was chosen to improve the infrared emissivity. For solar spectrum, hierarchical air pores were formed in the geopolymer matrix that can introduce gentle light scattering. Moreover, other types of powders were added into the AAGP matrix to further facilitate multiple Mie scattering of sunlight. Semiconductors with large bandgap and high refractive index are favored for efficient scattering.

(44) FIG. 2a shows the measured solar reflectance of the formed AAGP geopolymer coatings modified with commonly used white wide band gap materials including BaSO.sub.4; MgF.sub.2; BaTiO.sub.3; light-weight lime and ground lime. To avoid agglomeration of BaTiO.sub.3 powders and to avoid coagulation of light-weight lime, they were pre-treated with ethanol dissolved KH-800 silane coupling agent (the powders were immersed in KH-800 solution and then oven dried at 80 C. for one hour). Table 1 summarizes the reflectance of different coatings integrated in different spectral regions (i.e., UV region, VIS region and NIR region) and the resultant overall reflectance. It can be observed that, comparing to other white materials, BaSO.sub.4 enabled the AAGP coating with the highest reflectance in the UV range (0.8546) as well as a remarkable overall solar reflectance of 0.9690. Therefore, in spite of the difference existing between the polymeric and inorganic matrix, the dielectric contrast near geopolymer-air, geopolymer-BaSO.sub.4 and air-BaSO.sub.4 interfaces can efficiently introduce multiple Mie scattering and thus improves the overall solar reflectance.

(45) TABLE-US-00001 TABLE 1 Solar reflectance of AAGP coating with different additives in different spectral regions. Sample UV Vis NIR Overall AAGP Matrix 0.3429 0.8076 0.7364 0.7620 AAGP Matrix with BaSO.sub.4 0.8546 0.9791 0.9679 0.9690 AAGP Matrix with BaTiO.sub.3 0.6694 0.9292 0.9023 0.9064 AAGP Matrix with pre-treated BaTiO.sub.3 0.6419 0.9238 0.9016 0.9025 AAGP Matrix with pre-treated light-weight 0.6716 0.9357 0.9165 0.9165 AAGP Matrix with ground lime 0.6511 0.9259 0.9058 0.9058

(46) Further research was conducted to investigate how the addition ratio of BaSO.sub.4 in the AAGP matrix influences the solar reflectance the coating. Four different addition ratios of BaSO.sub.4 varying from 50 w % to 70 w % were selected. It is shown that as the addition ratio of BaSO.sub.4 increases, the solar reflectance of the AAGP coating increases first and then decreases (see FIG. 2b), with the maximum value overall reflectance reached at 60 wt % (i.e., 0.969). At the optimized addition ratio of BaSO.sub.4 (i.e., 60 wt %), different amounts of nano-SiO.sub.2 particles (0% to 2.5% of the matrix by weight) with high infrared emissivity were further added into the matrix to assist scattering. It is shown in FIG. 2c that addition of 1.5 wt % nano-SiO.sub.2 particles led to the best overall reflectance performance (i.e., 0.9758).

(47) FIG. 2d presents the measured spectral response of the thermal infrared (6-20 m) emissivity of the optimized AAGP cooling coating (i.e., with 60% BaSO.sub.4 and 1.5% SiO.sub.2). It is shown that the infrared emissivity both in and out of the sky window (8-13 m) was very high (0.9491). This high emissivity was attributed to the alumino-silicate network of geopolymer (SiOAl(Si)O).

Example 7Materials Characterizations

Example 8XRD Spectrum and FT-IR Spectrum

(48) As shown in FIGS. 3a and 3b, the characteristic peaks of the raw materials of the coating and the changes in crystal structure after the coating formation were analyzed by XRD tests. The characteristic peaks of metakaolin include broad dispersion peaks with low intensity between 20 and 28.4, indicating the mixed semi-crystalline and amorphous structure with strong reactivity, which facilitated the formation of geopolymer. The results show that the siloxane and aluminoxane tetrahedral structures in metakaolin disappeared to form three possible complex structural morphologies (AlOAl, SiOSi or SiOAl chains), which are presented as phase shifts in FIG. 3b.

(49) The diffraction peaks of BaSO.sub.4 are relatively sharp, indicating good crystallinity, high purity, and a hexagonal crystal structure (JCPDF file no. 24-1035). The characteristic peaks of BaSO.sub.4 can also be clearly observed after being added into AAGP matrix, as shown in FIG. 3b, which is a major function part of the cooling coating. The small amount of PTFE provided a small sharp characteristic peak at 18.5 (JCPDF file no. 54-1595) in the AAGP coating (FIG. 3b). Addition of Ca(OH).sub.2 hardly changed the crystalline structure of the AAGP coating.

(50) The functional groups of the raw materials and AAGP coating with different fillers were investigated through FTIR analysis, as shown in FIGS. 3c and 3d. The major characteristic peak of metakaolin locates at 1068 cm.sup.1 is in association with the SiO asymmetric vibration. However, it shifts to 1060 cm.sup.1 in the geopolymer matrix, which can be attributed to the partial replacement of [SiO.sub.4] tetrahedra by [AlO.sub.4] tetrahedra that alters the local chemical environment of the SiO bond. The characteristic bands centered at 798 cm.sup.1 and 777 cm.sup.1 in the metakaolin spectra are attributed to the stretching and bending vibrations of the six-coordinated AlO, which is a highly reactive component of the metakaolin. These two peaks changed to one moderate peak at 784 cm.sup.1 after geopolymerization, which is the vibration of unit of the geopolymer structure SiOAl or SiOSi. The above intensive peaks (at 9.434 m and 12.76 m) in the infrared atmospheric window contributed to the high emissivity of the geopolymer matrix. The characteristic bands of BaSO.sub.4 nanoparticle centered at 1060 cm.sup.1 and the shoulder at 984 cm.sup.1 were assigned to symmetric stretching vibration of SO.sub.4.sup.2 group. The peaks obtained at 637 and 603 cm.sup.1 were attributed to the out-of-plane bending vibration of the SO.sub.4.sup.2. As the BaSO.sub.4 content exceeds half of the total content, most of the peaks of the AAGP cooling coating exhibited its characteristic peaks.

Example 9SEM and Element Mapping Results

(51) The microscopic surface morphology of raw materials and AAGP coatings are shown in the FIG. 4. It is seen that the three-dimensional geopolymer matrix formed the scaffold that bound up the BaSO.sub.4 flakes and silica nanospheres, forming a surface morphology of intermingled micro-/nano-bulges and pores. Interestingly, hierarchical air pores were observed in the AAGP matrix, which is beneficial for enhancing solar reflectance.

(52) The element mapping of the coating surface was obtained by EDS analysis for which show the evenly distributed different chemical elements in the analyzed sample (FIG. 5).

Example 10Field Cooling Performance Tests

(53) The device (details are shown in Field Test Apparatus and FIG. 7) was placed on a flat building roof under direct sunlight on Nov. 13, 2021, in Hong Kong. The relative humidity was recorded stably at around 40%. The average wind speed was 3 m s.sup.1. FIG. 6a shows the variations of the ambient temperature and the surface temperatures of coated and uncoated cement boards within 24 hours and FIG. 6b shows the enlarged view during noon time (i.e., 11:00 am to 13:00 pm). It is shown that the surface temperature of AAGP coating was consistently lower than the ambient temperature at daytime.

(54) The detailed average temperature data of the uncoated board (T.sub.b), AAGP coating (T), and the ambient environment (T.sub.a) are presented in Table 2. The results show that the AAGP coating could achieve an average temperature reduction of 4.09 C. and a maximum temperature reduction of 8.9 C. compared to the ambient (i.e., T.sub.a-T), while the average and maximum temperature differences between AAGP coated and uncoated boards (i.e., T.sub.b-T) were 5.54 C. and 24.30 C., respectively.

(55) TABLE-US-00002 TABLE 2 Average temperatures of uncoated board and AAGP-coated board. Average ( C.) T.sub.b T T.sub.a T.sub.a T T.sub.b T 11 am to 1 pm 32.79 22.07 25.77 3.70 10.72 12 am to 12 pm 25.25 19.71 23.80 4.09 5.54

(56) In addition, our AAGP coating exhibits excellent durability under abrasion, water permeability, pull-out and TGA tests (see Examples 12-14), indicating a superior alternative for long-term large-scale applications of radiative cooling coatings.

Example 11Field Test Apparatus

(57) The device shown in the FIG. 7 was used to compare the surface temperature difference between uncoated and coated cement boards. The as-prepared AAGP cooling coating (with the optimized mix proportions) was sprayed onto the surface of a cement board and exposed to sunlight after the hydrophobic treatment as previously mentioned. A polystyrene foam frame covered by aluminum foil was prepared to support and insulate the coated and uncoated boards. A thermocouple was installed beneath the boards (substrates) and a datalogger was used to collect the temperature data. The ambient temperature and humidity were recorded by the weather station.

Example 12Results of Abrasion Tests

(58) FIG. 8a compares the thickness reduction of the AAGP coating at different linear abrasion distances performed on the standard sandpaper (mesh no. 340) with the 500 g abrasion load. It is shown that the thickness reduction of AAGP coating was about 16 m after 50 cm abrasion while such value is more than 40 m for a typical polymeric commercial coating. Therefore, the AAGP coating exhibited an approximately the same or even better abrasion resistance than the commercial coating, indicating a better long-term anti-wear property. FIG. 8b shows the solar reflectance of the AAGP coating before and after abrasion. The results show that the overall reflectance marginally changed after the abrasion (from 0.9758 to 0.9726, see Table 3). FIGS. 8c and 8d show the microscopic surface morphology of the AAGP coating before abrasion and after abrasion, which indicates that the three-dimensional structure combining the bumps and pores was well retained after the wearing test, i.e., the excellent optical properties of AAGP coating was maintained.

Example 13Results of Pull-Out Bond Test and Water Permeability Test

(59) The adhesion property of AAGP coating to substrate is very important for its engineering application. FIG. 9a presents the adhesion test results. The average bonding strength of three tests was approximately 2.48 M/Pa although the deviation was quite large (with mean absolute deviation of 0.68) and the failure mode was the substrate failure (FIG. 9b), indicating a good adhesion property. The waterproof performance of the AAGP coating was evaluated by water permeability test according to standard of Japan Society of Civil Engineers JSCE-K571-2004. The AAGP coated and uncoated substrate were respectively tested under three funnel tubes, which were placed upside down on their surface and filled in with water (FIG. 9c). The amount of water reduction was recorded after 7 days for each funnel tube. The test results show that the AAGP cooling exhibited a 2.12 mg/day/cm.sup.2 rate of water permeability as compared to the value of 3.9 mg/day/cm.sup.2 reported for the typical commercial coating. Water in the funnel tube sealed on the uncoated substrate was all gone. Therefore, the AAGP coating exhibited excellent water resistance, which is essential for outdoor applications.

Example 14Results of TGA Test

(60) TGA test was conducted on AAGP coatings with different additives and the results are shown in FIG. 10. The AAGP matrix lost 12.5% of the weight at 200 C. and 17.5% at 600 C.; The AAGP matrix with BaSO.sub.4 (60 wt %) and SiO.sub.2 (1.5 wt %) lost 2.5% of the weight at 200 C. and 5% at 400 C.; PTFE modified AAGP matrix with BaSO.sub.4 (60 wt %) and SiO.sub.2 (1.5 wt %) lost 3% at 200 C. and 5% at 400 C.; PTFE modified AAGP matrix with BaSO.sub.4 (60 wt %) and SiO.sub.2 (1.5 wt %) with Ca(OH).sub.2 (i.e. AAGP cooling coating) lost 3% at 200 C. and lost 5% at 400 C. It can be concluded that the AAGP matrix with BaSO.sub.4 (60 wt %) and SiO.sub.2 (1.5 wt %) had an excellent high temperature resistance compared to the matrix without any functional filler. Addition of a relatively small amount of PTFE emulsion and Ca(OH).sub.2 just marginally affected the high temperature resistance, while they are very helpful in achieving a good workability of the coating.

(61) TABLE-US-00003 TABLE 3 The solar reflectance of AAGP coating before and after abrasion test AAGP coating UV Vis NIR Overall before abrasion 0.9067 0.9863 0.9708 0.9758 after abrasion 0.8735 0.9813 0.9718 0.9726

(62) An inorganic geopolymer-based daytime radiative cooling coating has been developed in this study, which is environment-friendly and can be formed and cured at room temperature. Based on a comprehensive experimental study program, the following conclusions have been arrived: (1) The AAGP coating has achieved a high sky window emissivity of 0.9491 and 97.6% of solar reflectance mainly due to the addition of BaSO.sub.4 and nano-SiO.sub.2 particles and the hierarchical air pores formed in the AAGP matrix. (2) The optimized AAGP coating could achieve a sub-ambient cooling effect up to 8.9 C. under direct sunlight. (3) The developed AAGP coating could maintain well its performance after mechanical wearing and high temperature exposure and exhibits good waterproofing resistance. (4) Due to the inherit advantages of an inorganic coating over its organic counterpart, the developed AAGP coating is expected to be able to broaden the applicability of the DRC technology for efficient thermal management and energy saving purpose.