Fire resistant corrosion protective water proofing energy saving water based heat insulating coating composition

Abstract

The present disclosure relates to coating compositions. A fire resistant, corrosion protective, water proofing, energy saving, water based heat insulating coating composition and a process for its preparation is provided. The coating composition comprises a graft copolymer emulsion, a colorant, and one or more reinforcing additives. The graft copolymer is crafted to synergize the properties shown by the polymers of four different specialty monomers which results in a coating that exhibits excellent heat insulation and other mechanical properties. The coating is useful as a heat insulating coating.

Claims

1. A water based heat insulating coating composition, said composition comprising: (a) 30% to 60% of a graft copolymer emulsion, said emulsion comprising at least one graft copolymer comprising a hard segment monomer, a soft segment monomer, a first reinforcing monomer, and a second reinforcing monomer; (b) 15% to 30% of a colorant; (c) 5% to 25% of at least one reinforcing additive; and (d) QS for 100%, water.

2. The coating composition as claimed in claim 1, wherein the ratio of said hard segment monomer and said soft segment monomer in the graft copolymer of said graft copolymer emulsion is in the range of 40:60 to 80:20 wt %.

3. The coating composition as claimed in claim 1, wherein the graft copolymer of said graft copolymer emulsion comprises said hard segment monomer in the range of 10% to 60%, said soft segment monomer in the range of 10% to 60%, said first reinforcing monomer in the range of 2% to 20% and said second reinforcing monomer in the range of 1% to 10%.

4. The coating composition as claimed in claim 1, wherein said hard segment monomer is at least one selected from the group consisting of methacrylates, styrene and alpha-methyl styrene, said soft segment monomer is at least one acrylate, said first reinforcing monomer is acetoacetoxy ethyl methacrylate and said second reinforcing monomer is maleic anhydride.

5. The coating composition as claimed in claim 1, wherein said reinforcing additive is selected from the group consisting of nano graphite, nano zinc oxide, magnesium hydroxide, aluminum trihydrate, antimony trioxide and pentaerythritol.

6. The coating composition as claimed in claim 1, wherein said emulsion comprises at least one functional additive.

7. The coating composition as claimed in claim 6, wherein said functional additive is a coalescing agent selected from the group consisting of tributyl phthalate and glycols.

8. A process for preparing a water based heat insulating coating composition, said process comprising: (a) preparing a graft copolymer emulsion by: (i) providing water, an emulsifier, a buffer and a freeze-thaw agent in a reactor maintained at a temperature in the range of 25° C. to 40° C. and speed of agitation in the range of 10 rpm to 50 rpm; (ii) heating the reactor to a temperature in the range of 50° C. to 80° C. and adding a hard segment monomer and at least one functional additive to the reactor to obtain a first reaction mixture; (iii) adding a polymerization initiator dissolved in water to said first reaction mixture at a feed rate in the range of 2 ml/min to 20 ml/min to initiate polymerization of said hard segment monomer and to obtain a growing hard segment polymer backbone; (iv) adding a first reinforcing monomer at a feed rate in the range of 2 ml/min to 20 ml/min to the reactor to initiate grafting of said first reinforcing monomer onto the growing hard segment polymer backbone; (v) on complete addition of said first reinforcing monomer, adding a first mixture comprising at least one soft segment monomer and at least one functional additive, at a feed rate in the range of 2 ml/min to 20 ml/min to the reactor and initiating grafting of said soft segment monomer onto the growing hard segment polymer backbone and initiate polymerization of said soft segment monomer to obtain a growing soft segment polymer backbone; (vi) on complete addition of said first mixture, adding the first reinforcing monomer at a feed rate in the range of 2 ml/min to 20 ml/min to initiate grafting of the first reinforcing monomer onto the growing soft segment polymer backbone; and (vii) on complete addition of said first reinforcing monomer in substep (vi), adding a second mixture comprising said second reinforcing additive and at least one functional additive to the reactor to initiate grafting of the second reinforcing monomer onto the backbones of the growing hard segment polymer and growing soft segment polymer and continuing the reactions for a time period in the range of 2 to 6 hours and then cooling to obtain said graft copolymer emulsion; (viii) isolating said graft copolymer emulsion from the reactor in a vessel to obtain an isolated graft copolymer emulsion; (b) adding a colorant to said isolated graft copolymer emulsion in the vessel while stirring; and (c) adding at least one reinforcing additive to the vessel after step (b) while stirring to obtain said water based heat insulating coating composition.

9. The process as claimed in claim 8, wherein the water to total monomer ratio is in the range of 50:50 to 70:30.

10. The process as claimed in claim 8, wherein said soft segment monomer and said hard segment monomer are interchanged.

11. The process as claimed in claim 8, wherein said soft segment monomer and said hard segment monomer are added in a continuous and controlled manner at a feed rate in the range of 2 ml/min to 20 ml/min.

12. The process as claimed in claim 8, wherein said hard segment monomer is at least one selected from the group consisting of methacrylates, styrene and alpha-methyl styrene, said soft segment monomer is at least one acrylate, said first reinforcing monomer is acetoacetoxy ethyl methacrylate and said second reinforcing monomer is maleic anhydride.

13. The process as claimed in claim 8, wherein said reinforcing additive is selected from the group consisting of nano graphite, nano zinc oxide, magnesium hydroxide, aluminum trihydrate, antimony trioxide, and pentaerythritol.

14. The process as claimed in claim 8, wherein said buffer is ammonium hydroxide and said emulsifier is selected from the group consisting of sodium laureth sulphate and lecithin.

15. The process as claimed in claim 8, wherein said polymerization initiator is selected from the group consisting of ammonium persulphate, azobisisobutyronitrile and benzoyl peroxide.

16. The process as claimed in claim 8, wherein said freeze-thaw agent is isopropyl alcohol.

Description

BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWING

[0048] The water based heat insulating coating composition of the present disclosure will now be described with the help of the accompanying drawing, in which:

[0049] FIG. 1 illustrates a representational FIGURE of internal branching between the hard segment monomer, soft segment monomer, and the first and the second reinforcing monomers of the graft copolymer of the present disclosure to give a cross-linked like appearance.

DETAILED DESCRIPTION

[0050] Solvent based heat insulating coatings are not eco-friendly due to their release of dangerous VOCs into the environment. Water based heat insulating coatings in the state-of-the-art suffer from a lack of good mechanical properties and require frequent maintenance as their performance decreases with time.

[0051] The present disclosure, therefore, envisages a heat insulating coating composition that synergizes the advantages of both solvent based and water based heat insulating coatings. The desired performance properties of heat insulating coatings are: [0052] Excellent Solar Reflectivity Index (SRI) and emissivity values [0053] Resistance to UV radiation [0054] Scratch resistance [0055] Toughness [0056] Chemical Resistance [0057] Flexibility [0058] Thermal stability [0059] Easy application onto various substrates like metal, concrete, wood, paper, FRP and the like [0060] Forming a stable emulsion [0061] Fire resistance [0062] Eco-friendliness [0063] Single-pack system for ready use [0064] Fast drying at ambient temperatures

[0065] In the coating composition, the only critical component responsible for the performance of the coating is the polymer. The type of polymer used determines the service performance of the coating.

[0066] The minimum required properties to be shown by the polymer are:

[0067] Heat Insulation Performance

[0068] Key parameters of heat insulation performance are SRI, emissivity of the material and thermal emittance of the coating (lambda values). SRI values should be higher, emissivity and emittance values should be lower for the polymer and finally the coating.

[0069] Protection Against Oxygen and Water

[0070] The film made by the polymeric coating should have excellent resistance to moisture and impermeability to oxygen.

[0071] UV Radiation Resistance

[0072] Many polymers when subject to UV attack from the sun, begin to degrade and lose their performance. The coating must be resistant to UV radiation.

[0073] Chemical Resistance

[0074] Many polymers are subject to attack by various chemicals like acids, alkalis, chlorine gas and ammonia gas. The coat surface gets corroded or the coat peels off when exposed to these chemicals. The polymer should resist attack from such chemicals.

[0075] Scratch and Abrasion Resistance

[0076] The outside and the inside of buildings are subject to various abuses either due to humans, stray animals, birds or other natural factors. These factors may cause scratches or abrasion due to which the underlying surface may get exposed and cause deterioration of the substrate. The polymer should, therefore, have excellent scratch resistance.

[0077] Freeze-Thaw Resistance

[0078] In regions subject to heavy rainfall and severe cold and hot weathers, freeze-thaw weathering can cause cracking of the polymeric coating films and the concrete structures beneath them. The accumulative effect of successive freeze-thaw cycles can be dangerous to the construction. The coat should therefore exhibit freeze-thaw resistance.

[0079] Thermal Stability

[0080] The coated surface may get exposed to very high temperatures. The coat should not soften, melt or break under such conditions. This will also peel off the film and expose the substrate beneath.

[0081] Flexibility and Fatigue Endurance

[0082] Metal undergoes continual expansion and contraction with the variation in temperature caused due to weather changes. The film should be flexible to absorb expansion and contraction without cracking. Most importantly, the coat should not reduce in performance due its flexibility.

[0083] Fire Resistance

[0084] Since coatings come in close proximity to human life, safety is of prime importance. In the event of fire, these coatings should not assist spreading the fire. They should resist the fire and protect the surface for a long time to minimize the loss of lives and property.

[0085] No single monomer based polymer (homopolymer) can fulfill all the desired properties. So, the idea is to prepare a graft copolymer that synergizes the properties shown by the polymers of four different specialty monomers—a hard segment monomer, a soft segment monomer, a first reinforcing monomer and a second reinforcing monomer and use the graft copolymer in the form of an emulsion as a coating composition. The four specialty monomers are so grafted as to form an internal branching similar to cross-linking which increases the resistance to environmental abuses. The final coating composition should be capable of cross-linking which will have enhanced performance over non-crosslinked coats. The cross-linking should be achieved without the use of a hardener or crosslinking agent.

[0086] Hard segment monomers impart toughness, UV stabilization, scratch and abrasion resistance. Soft segment monomers impart flexibility, impact resistance, elongation, moisture resistance, and impermeability. The reinforcing monomers impart good adhesion properties, surface hardness, weathering and aging resistance. The resultant graft copolymer will have a combination of all these properties and on curing will provide excellent heat insulation properties.

[0087] The desired properties of the coating composition is achieved by appropriate selection of the four monomers, designing the polymerization process to achieve a graft structure, selecting a colorant and a reinforcing additive for achieving the desired heat insulation properties.

[0088] In accordance with one aspect of the present disclosure, a water based heat insulating coating composition is provided herein. The composition comprises: [0089] (a) 30% to 60% of a graft copolymer emulsion; [0090] (b) 15% to 30% of a colorant; [0091] (c) 5% to 25% of at least one reinforcing additive; and [0092] (d) QS for 100%, water.

[0093] The graft copolymer emulsion comprises at least one graft copolymer comprising a hard segment monomer, a soft segment monomer, a first reinforcing monomer and a second reinforcing monomer. In addition to the graft copolymer, the emulsion may contain at least one functional additive.

[0094] The colorant, essentially, comprises at least one organic or/and inorganic pigment. In addition to the pigments, the colorant may contain a dispersing medium, functional fillers and water. The functional filler is at least one selected from the group consisting of mica, silica, barium sulphate, talc, china clay, calcium carbonate, ceramic, and zinc phosphate.

[0095] In an embodiment, the colorant comprises a pigment in the range of 10% to 60%, the dispersing medium in the range of 15% to 55%, the functional fillers in the range of 2% to 20% and water in the range of 10% to 50%. In a particular embodiment, the dispersing medium is a hydroxyl ethyl cellulose solution in water.

[0096] The reinforcing additives may be used in raw form or dispersed in a dispersing medium and water before being added to the coating composition. In an embodiment, a mixture of 10% to 60% of the reinforcing additives, 15% to 55% of the dispersing medium and 2% to 20% water is used as component (c) in the coating composition. In a particular embodiment, the dispersing medium is a hydroxyl ethyl cellulose solution in water.

[0097] The amount of the hard segment monomer in the graft copolymer is in the range of 10% to 60% while the amount of the soft segment monomer is in the range of 10% to 60%. The hard segment monomer:soft segment monomer ratio in the copolymer is in the range of 40:60 to 80:20. The amount of the first reinforcing monomer is in the range of 2% to 20% of the graft copolymer whereas the amount of the second reinforcing monomer is in the range of 1% to 10% of the graft copolymer.

[0098] The hard segment monomer is at least one selected from the group consisting of methacrylates, styrene and alpha-methyl styrene, the soft segment monomer is at least one acrylate, the first reinforcing monomer is acetoacetoxy ethyl methacrylate (AAEM) and the second reinforcing monomer is maleic anhydride. In an embodiment, the functional additive is a coalescing agent selected from the group consisting of tributyl phthalate (TBP) and glycols. The amount of the coalescing agent is in the range of 0.5% to 1.5% of each monomer.

[0099] The reinforcing additive is selected from the group consisting of nano graphite, nano zinc oxide, magnesium hydroxide, aluminum trihydrate, antimony trioxide and pentaerythritol.

[0100] In accordance with another aspect of the present disclosure, a process for the preparation of a water based heat insulating coating composition is provided herein.

[0101] A reactor is provided with stirring means and temperature control with multiple inlets. Water, an emulsifier, a buffer and a freeze-thaw agent are then fed into the reactor maintained at a temperature in the range of 25° C. to 40° C. and speed of agitation in the range of 10 rpm to 50 rpm. The emulsifier is selected from the group consisting of sodium laureth sulphate (SLES) and lecithin. The buffer is used to maintain the pH of the emulsion. In an exemplary embodiment, the buffer used is ammonium hydroxide. The buffer is used in an amount in the range of 0.1% to 0.8% of water fed into the reactor. In an exemplary embodiment, the freeze-thaw agent used is isopropyl alcohol (IPA).

[0102] The water to total monomer ratio is one of the determining factors of the final properties of the coat. The amounts of water and monomers are so chosen as to achieve a water:total monomer ratio in the range of 50:50 to 70:30.

[0103] The reactor is then heated to a temperature in the range of 50° C. to 80° C. followed by the addition of a hard segment monomer and at least one functional additive. The entire quantity of the hard segment monomer and the functional additive is added at once. The hard segment monomer is at least one selected from the group consisting of methacrylates, styrene, and alpha-methyl styrene.

[0104] In an embodiment, the functional additive is a coalescing agent selected from the group consisting of TBP and glycols. The amount of the coalescing agent is in the range of 0.5% to 1.5% of the hard segment monomer.

[0105] A polymerization initiator dissolved in water is then continuously added at a feed rate in the range of 2 ml/min to 20 ml/min to initiate polymerization of the hard segment monomer and to obtain a growing hard segment polymer backbone. The polymerization initiator is selected from the group consisting of ammonium persulphate, azobisisobutyronitrile, and benzoyl peroxide. The amount of the polymerization initiator used is in the range of 0.1% to 2.0% of the combined amount of the monomers.

[0106] As the exotherm rises and the temperature of the reactor increases to a value in the range of 70° C. to 95° C., a first reinforcing monomer at a feed rate in the range of 2 ml/min to 20 ml/min is added to the reactor to initiate grafting of the first reinforcing monomer onto the growing hard segment polymer backbone. In an embodiment, the first reinforcing monomer is AAEM.

[0107] On complete addition of the first reinforcing monomer, a first mixture comprising at least one soft segment monomer and at least one functional additive is added at a feed rate in the range of 2 ml/min to 20 ml/min to the reactor to initiate grafting of the soft segment monomer onto the growing hard segment polymer backbone and also to simultaneously initiate polymerization of the soft segment monomer and to obtain a growing soft segment polymer backbone. The soft segment monomer is at least one selected from acrylates. In an embodiment, the functional additive is a coalescing agent selected from the group consisting of TBP and glycols. The amount of the coalescing agent is in the range of 0.5% to 1.5% of the soft segment monomer.

[0108] On complete addition of the first mixture, the first reinforcing monomer is again introduced at a feed rate in the range of 2 ml/min to 20 ml/min to initiate grafting of the first reinforcing monomer onto the growing soft segment polymer backbone.

[0109] When the entire quantity of the first reinforcing monomer has been added, a second mixture comprising the second reinforcing additive and at least one functional additive are added to the reactor to initiate grafting of the second reinforcing monomer onto the backbones of the growing hard segment polymer and growing soft segment polymer. The second reinforcing monomer is maleic anhydride. In an embodiment, the functional additive is a coalescing agent selected from the group consisting of TBP and glycols.

[0110] The grafting and polymerization reactions are continued for a time period in the range of 2 to 6 hours. The reactor is then cooled to a temperature in the range of 25° C. to 40° C. to obtain the graft copolymer emulsion comprising the graft copolymer comprising the hard segment monomer, the soft segment monomer, the first reinforcing monomer and the second reinforcing monomer. The graft copolymer emulsion from the reactor is then isolated in a separate vessel to obtain an isolated graft copolymer emulsion. The amount of the hard segment monomer in the graft copolymer is in the range of 10% to 60%. The amount of the soft segment monomer in the graft copolymer is in the range of 10% to 60%. The hard segment monomer:soft segment monomer ratio in the copolymer is in the range of 40:60 to 80:20. The amount of the first reinforcing monomer is in the range of 2% to 20% of the graft copolymer while the amount of the second reinforcing monomer is in the range of 1% to 10% of the graft copolymer.

[0111] This results in a copolymer with the backbone made of the hard segment polymer and the soft segment polymer is grafted onto the hard segment polymer backbone. The reinforcing monomers are grafted onto both the hard segment and the soft segment polymers.

[0112] The hard segment monomer and the soft segment monomer are taken in amounts such that the hard segment monomer:soft segment monomer ratio is in the range of 40:60 to 80:20.

[0113] In an embodiment of the present disclosure, the soft segment monomer and the hard segment monomer are interchanged. This results in a copolymer with the backbone made of the soft segment polymer and the hard segment polymer is grafted onto the soft segment polymer backbone. The reinforcing monomers, again, are grafted onto both the hard segment and the soft segment polymers. By varying the process conditions, the amounts of the hard and the soft segment monomers and their way of addition selected from discrete and continuous, graft copolymers with a number of grafting patterns can be prepared. They include soft on hard, hard on soft, hard-soft-hard, soft-hard-soft and random.

[0114] In another embodiment of the present disclosure, the hard segment monomer, the soft segment monomer and the reinforcing monomers are not added entirely but at continuous and controlled feed rates independent of each other. The feed rates independently vary in the range of 2 ml/min to 20 ml/min. In still another embodiment, the hard segment monomer is added at a continuous and controlled feed rate while the soft segment monomer is added all at once.

[0115] Various permutations and combinations in the amounts of the four monomers and their way of addition selected from discrete and continuous are permissible to result in graft copolymers having all possible grafting patterns and hence, properties.

[0116] FIG. 1 illustrates a representational FIGURE of the structure of one such graft copolymer of the present disclosure wherein A represents a hard segment monomer, B represents a soft segment monomer, C represents the first reinforcing monomer and D represents the second reinforcing monomer.

[0117] A colorant is now added to the isolated graft copolymer emulsion in the vessel while stirring. The colorant, essentially, comprises at least one organic or/and inorganic pigment. It may comprise a dispersing medium, functional fillers and water in addition to the pigments, to help disperse the pigments in the graft copolymer emulsion. In an embodiment, the colorant comprises the pigments in the range of 10% to 60%, a dispersing medium in the range of 15% to 55%, the functional fillers in the range of 2% to 20% and water in the range of 10% to 50%.

[0118] At least one reinforcing additive is then added to the vessel containing the isolated graft copolymer emulsion and the colorant while stirring to obtain the water based heat insulating coating composition. The reinforcing additive may be used in raw form or mixed with a dispersing medium and water before being added to the graft copolymer emulsion. In an embodiment, a mixture comprising 10% to 60% of the reinforcing additives, 15% to 55% of the dispersing medium and 10% to 50% water is added to the graft copolymer emulsion.

[0119] The amounts of colorants and reinforcing additives are so taken such that the final water based heat insulating coating composition comprises colorants in the range of 15% to 30% of the coating composition and the reinforcing additives in the range of 5% to 25% of the coating composition. QS to make 100% of the coating composition is fulfilled by adding water.

[0120] The water based coating composition of the present disclosure has all the desired properties like fire resistance, corrosion resistance, water proofing, and heat insulation and hence is energy saving.

[0121] The present disclosure is further described in light of the following laboratory experiments which are set forth for illustration purpose only and not to be construed for limiting the scope of the disclosure. The following experiments can be scaled up to industrial/commercial scale and the results obtained can be extrapolated to industrial scale.

[0122] Experiments

[0123] Experiment 1

TABLE-US-00001 TABLE 1 Various ingredients used in the preparation of a hard-soft- hard graft copolymer emulsion based coating composition Part I 1. Distilled Water - 460 g 2. Emulsifier - SLES - 10 g 3. Buffer - NH.sub.4OH - 4.6 g 4. Freeze-Thaw Agent - IPA - 3.3 g Part II 1. Distilled water - 520 g 2. Initiator - AIBN/BPO - 1.5 g Part III 1. Methacrylate monomer- 128 g 2. Coalescing agent - TBP - 1.5 g Part IV 1. Acetoacetoxy ethyl methacrylate - 55 g Part V 1. Acrylate Monomer - 170 g 2. Coalescing agent - TBP - 1.2 g Part VI 1. Acetoacetoxy ethyl methacrylate - 55 g Part VII 1. Styrene Monomer - 85 g 2. Maleic Anhydride - 5 g 3. Methacrylic Acid - 17 g 4. Coalescing agent - TBP - 1.2 g

[0124] Table 1 shows the various ingredients used in the preparation of a hard-soft-hard graft copolymer emulsion based coating composition.

[0125] Step 1

[0126] Part I was taken in a round bottom flask fitted with a stirrer, a condenser, feeding funnels, a temperature sensor in a water bath. Speed of agitation was maintained at 50 rpm. The temperature of the contents was raised from room temperature to 50° C. with constant stirring.

[0127] Step 2

[0128] Part III was added in the reaction in the entire amount followed by part II which was fed at a constant feed rate of 10 ml per minute.

[0129] Step 3

[0130] When the exotherm started building up, part IV was added at a temperature of reaction of 75° C. at a speed of 10 ml per minute.

[0131] Step 4

[0132] Once the addition of part IV was completed, part V was added at a reaction temperature of 75° C. at a speed of 10 ml per minute.

[0133] Step 5

[0134] Once the addition of part V was completed, part VI was added at a reaction temperature of 75° C. at a speed of 10 ml per minute.

[0135] Step 6

[0136] Once the addition of part VI was completed, part VII was added at a reaction temperature of 75° C. at a speed of 10 ml per minute.

[0137] Step 7

[0138] The reaction was allowed to continue at 75° C. for 6 hrs.

[0139] Step 8

[0140] The reactor was cooled to 35° C. after step 7.

[0141] Step 9

[0142] The reactants were drained and filtered under vacuum.

[0143] The copolymer thus formed was mixed with a colorant and a reinforcing additive to result in the coating composition.

[0144] Experiment 2

[0145] Coating Process

[0146] The coating composition obtained from Experiment 1 was transferred into a conventional air assisted spray type pot gun. The air pressure and the volume as per the object profile were adjusted. A first coat was uniformly applied over the entire surface which was shot blasted to Sa21/2 level. The coat was allowed to dry for 30 minutes. A second coat was uniformly applied over the first coat which was allowed to dry for 30 minutes. The coated object was ready to handle/use after 60 minutes of coating.

[0147] Experiment 3

[0148] Testing of the water based coating composition of experiment 1 was carried out by preparing a test panel. A mild steel panel of 1 to 1.5 mm thickness having a dimension of 150*100 mm was used for the test. It was shot blasted to Sa 21/2 level using the water based coating composition of experiment 1. Two coats of the coating composition were applied with an interval of 30 minutes and the test panel was allowed to flash dry for 60 minutes to achieve a final dry film thickness (DFT) of 80 to 90 microns. For testing, the coated panel was force dried at 90° C. for 30 minutes.

[0149] The following tests were conducted as per ASTM standards [0150] A. Adhesion [0151] B. Cracking resistance [0152] C. Scratch Hardness [0153] D. UV Radiation Resistance [0154] E. Thermal Stability [0155] F. Corrosion Resistance [0156] G. Fire Resistance

[0157] Table 2 shows the results of the various tests performed.

TABLE-US-00002 TABLE 2 Test results of Experiment 3 Sr. No. Performance Test ASTM STD. ACTUAL 01 Solar Reflectivity — 113 Emissivity  0.82 02 Scratch Hardness D - 7027 No Exposure of (4.7 KG) Metal Substrate Passes the Test 03 Conical mandrel for D - 522 No film cracking resistance cracking or (4 mm) crazing 04 Adhesion D - 3359 No Peel-Off 05 Salt Spray Resistance B - 117 No Surface (Corrosion Resistance) Deterioration & 1000 HRS corrosion. (At 80 Microns DFT) 06 Thermal Stability at D - 2243 No effect on 200° C. for 24 hr coating surface. 07 UV Resistance D-4587-05 No Chalking 1000 hr Uv-b-313 nm-1 No color change 08 Resistance To Fire IS-163 Fire Spread Class I

[0158] From Table 2, it can be seen that the Solar Reflectivity value is considerably high and the Emissivity value is low. This shows that the coating composition of Example 1 has high heat insulation properties. Also, it can be seen from the above test results that the coating has very good scratch hardness, cracking resistance, adhesion, corrosion resistance, thermal stability, UV resistance and fire resistance.

[0159] Experiment 4

[0160] Two test panels were prepared by a method similar to Example 3. One test panel was coated with the coating composition of Experiment 1 and the other test panel was coated with a conventional acrylic emulsion coating. A comparison of properties of the two test panels is as follows:

TABLE-US-00003 TABLE 3 Comparison between a conventional coating and the coating of the present disclosure COATING COMPOSITION OF SR. CONVENTIONAL THE PRESENT NO. PARAMETERS COATINGS DISCLOSURE 1. Chemical Water based Graft Copolymer composition methacrylate with specialty polymer with functional ceramic hollow monomers and spheres additives 2. Application Two pack System: Single pack: system Requires mixing ready to use. of paint No mixing &cross-linker required. 3. SRI 78 103 4. Coating 700-800 microns 80 microns Thickness 3. Drying time 4 to 6 hr 15 minutes 4. Application Only Concrete. Applicable on Surface Not applicable all surfaces like on metal concrete, metal, wood, paper, cement boards and the like 5. Retention of Poor. Degrades Excellent Properties with time under Retention UV radiation Properties. No (Sunlight), effect of Rains, chemical Sunlight, rains, attack and chemicals and abrasive action. abrasive action. 6. Temperature 5 to 6° C. 10 to 14° C. Difference 7. Resistance NIL Excellent to fire Resistance to fire 8. Corrosion Fair Excellent Resistance 9. Waterproof Fair Excellent Properties Waterproofing properties 8. Maintenance Not washable. Zero maintenance. Difficult to Easy to clean and maintain. Oil wash. stains cannot Stain free. be removed.

[0161] From table 3, it can be seen that as compared to the conventional coating composition, the composition of the present disclosure has far more superior properties. It is a single pack system with good heat insulation properties shown even by thin films. The drying time of the composition of the present disclosure is less and can conveniently be applied over a range of surfaces. The present coating shows excellent corrosion resistance properties, waterproofing, fire resistance and other mechanical properties. Due to improved heat insulation, the water based heat insulating coating is energy saving.

[0162] The water based heat insulating coating composition of the present disclosure has the following performance properties and application features:

[0163] Performance Properties: [0164] 1. Excellent values of SRI & Emissivity indicating excellent heat insulation [0165] 2. Excellent Resistance to UV Radiation [0166] 3. Excellent Corrosion Resistance [0167] 4. Very Good Resistance to Chemicals [0168] 5. Service Temperature range: −40° C. to 250° C. [0169] 6. Very good scratch hardness [0170] 7. Excellent Moisture resistance and [0171] 8. Resistance to Fire

[0172] Application Features: [0173] 1. It is a single pack, ready to use system. No separate mixing procedure is required; [0174] 2. Quick drying at room temperature-Test panels dry within 30 minutes without the need for oven baking; [0175] 3. Easy application procedure—Can be applied using conventional application tools like brush, roller, airless and air assisted spray gun; and [0176] 4. Excellent adhesion on all substrates like steel, wood, glass, concrete, FRP and asbestos.

[0177] Technical Advances and Economical Significance

[0178] The present disclosure described herein above has several technical advantages including, but not limited to, the realization of a water based heat insulating coating composition that: [0179] is fire resistant, corrosion protective, water proofing, energy saving and has excellent mechanical properties; [0180] is eco-friendly; and [0181] is easy to apply on all substrates.

[0182] The foregoing description of the specific embodiments so fully reveals the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.

[0183] Throughout this specification the word “comprise”, or variations such as “comprises” or “comprising”, will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

[0184] The use of the expression “at least” or “at least one” suggests the use of one or more elements or ingredients or quantities, as the use may be in the embodiment of the disclosure to achieve one or more of the desired objects or results.

[0185] Any discussion of documents, acts, materials, devices, articles or the like that has been included in this specification is solely for the purpose of providing a context for the disclosure. It is not to be taken as an admission that any or all of these matters form a part of the prior art base or were common general knowledge in the field relevant to the disclosure as it existed anywhere before the priority date of this application.

[0186] The numerical values mentioned for the various physical parameters, dimensions or quantities are only approximations and it is envisaged that the values higher/lower than the numerical values assigned to the parameters, dimensions or quantities fall within the scope of the disclosure, unless there is a statement in the specification specific to the contrary.

[0187] While considerable emphasis has been placed herein on the components and component parts of the preferred embodiments, it will be appreciated that many embodiments can be made and that many changes can be made in the preferred embodiments without departing from the principles of the disclosure. These and other changes in the preferred embodiment as well as other embodiments of the disclosure will be apparent to those skilled in the art from the disclosure herein, whereby it is to be distinctly understood that the foregoing descriptive matter is to be interpreted merely as illustrative of the disclosure and not as a limitation.