The present invention is related to a coating and its forming method, and more particularly to an environmental water-borne quartz coating and a method for forming the same.
Most traditional interior/exterior wall latex coatings contain harmful substances, such as formaldehyde. Though formaldehyde can be used as a preservative and has advantages of increasing adhesion ability and inhibiting insect eggs, now formaldehyde is determined by World Health Organization as a carcinogenic and baby-deforming substance. In addition, releasing of formaldehyde from architecture coatings can be lasted for 3 to 15 years, and is greatly harmful to human health, mainly in olfactory abnormalities, allergies, abnormal lung function, abnormal liver function, and abnormal immune function.
Therefore, in recent years, formaldehyde-free coatings, even deformaldehyde coatings, have gradually replaced conventional latex coatings. However, how to form a coating capable of improving the living environment, and also having good covering ability is still a research topic and a development trend for coating manufacturers.
From the above, the present invention is to provide an environmental water-borne coating and a method for forming the same. The coating is not only without harmful substances, but also has good covering ability.
To achieve the above purpose, the present invention provides a coating including a composition of 5% to 10% by weight of water, 5% to 20% by weight of silica sol, 0.05% to 0.2% by weight of KH-560 silane coupling agent, and 20% to 60% by weight of quartz powder.
The present invention also provides a method for forming the coating, includes steps of:
The advantage of the present invention is that the coating with the above composition and forming method not only can effectively improve our living environment, but also has good covering ability. Besides, the coating can be used in high and low-temperature environment, and is without cracking. The forming process thereof is simple and is easy for commercial production.
The present invention will be best understood by referring to the following detailed description of some illustrative embodiments in conjunction with the accompanying drawing, in which
The sole FIGURE is a flowchart of a forming method for a quartz coating according to an embodiment of the present invention.
The following illustrative embodiments and drawings are provided to illustrate the disclosure of the present invention, these and other advantages and effects can be clearly understood by persons skilled in the art after reading the disclosure of this specification. First, the composition and weight percentages of a coating according to an embodiment of the invention are shown in Table 1.
Besides, each component of the coating with the above weight percentage can achieve:
Water
Silica Sol
KH-560 Silane Coupling Agent
Wetting Agent
Phthalein White Powder
Modified Bentonite
Quartz Powder
Styrene-Acrylate Emulsion
Pure Acrylate Emulsion
Carboxymethyl Cellulose
Crosslinking Agent
Fungicide
Deodorant
Defoaming Agent
The composition and weight percentages of a quartz coating of an embodiment according to the present invention is shown in Table 2. In this embodiment, water includes reverse osmosis water, distilled water, or tap water without impurities. Besides, the weight ratio of silica sol to the KH-560 silane coupling agent is 100:1.
Each weight percentage of the silica sol and the KH-560 silane coupling agent in the coating composition, and the relative ratio thereof are critical to the characteristic of the coating. Wherein, when the relative ratio of silica sol to the KH-560 silane coupling agent is 100:1, the quartz powder can be uniformly dispersed in the coating. If the quartz powder is not uniformly dispersed in the coating, it will cause the coating film on a wall become cracked. The quartz powder of this embodiment includes grain sizes of 400 to 2500 mesh. However, in other embodiments, the grain size of the quartz powder is not limited thereto. Besides, in this embodiment, the viscosity tested with a Stormer viscosmeter is 70 to 80 KU.
Besides, a forming method for the coating of this embodiment is shown in the sole FIGURE, including steps of A to D:
Step A: Adding water, silica sol, and the KH-560 silane coupling agent into an agitating equipment according to the weight percentages shown in Table 2, and agitating with a speed of 40 to 60 rpm for 25 to 35 minutes to form a decomposing agent.
In the above forming process of the quartz coating of this embodiment, preferably, the agitation speed of this step is 50 rpm, and the agitation time is 30 minutes. Besides, the adding sequence of silica sol and KH-560 silane coupling agent is not limited. That is, adding the KH-560 silane coupling agent first and then adding the silica sol will not affect the formation of the coating.
Step B: Adding the wetting agent, the phthalein white powder, the modified bentonite, the quartz powder and the styrene-acrylate emulsion into the agitating equipment according to the relative weight percentages shown in Table 2, and agitating with 1090 to 1100 rpm for 15 to 25 minutes to mix the above components with the decomposing agent to form a mixing agent. Wherein, the styrene-acrylate emulsion can be replaced with a pure acrylate emulsion.
In this embodiment, the agitation speed of the above step in the quartz coating forming process is preferably 1100 rpm, and the agitation time thereof is preferably 20 minutes. Besides, since the weight percentages of wetting agent, phthalein white powder and modified bentonite are small, the adding sequence thereof is not limited. In other words, in other embodiments, the components can be added into the agitating equipment with a replaceable sequence. For example, the wetting agent, the phthalein white powder and the modified bentonite can be added first, and then the quartz powder and the styrene-acrylate emulsion (or pure acrylate emulsion) are added so as to utilize each component's function effectively.
Step C: Adding the carboxymethyl cellulose, the crosslinking agent, the fungicide and the deodorant into the agitating equipment according to the weight percentages shown in Table 2, and agitating with 890 to 910 rpm for 15 to 25 minutes to mix the above components with the mixing agent to form a thickened mixing agent.
In this embodiment, the agitation speed of this step in the forming process of the quartz coating is preferably 900 rpm, and the agitation time is preferably 20 minutes. Besides, in other embodiments, the adding sequence of the components is not limited.
Step D: Adding the defoaming agent into the agitating equipment according to the weight percentage shown in Table 2, and agitating with 290 to 310 rpm for 85 to 95 minutes to mix the deforming agent with the thickened mixing agent to remove foams from the thickened mixing agent so as to form the quartz coating.
In this embodiment, the agitation speed in this step of the forming process of the quartz coating is preferably 300 rpm, and the agitation time thereof is preferably 90 minutes.
Besides, in Step D, a Stormer viscometer is utilized to measure the viscosity of the quartz coating. The final viscosity thereof is 70 to 80 KU. By the way, in practice, the agitating equipment utilized in the above forming method includes an agitator, a stirring barrel, or a Banbury mixer.
In summary, the environmental water-borne coating of the present invention utilizes a water-based forming method. Its manufacturing process is simple and easy for commercial production. Besides, the quartz coating is characterized in that, it is an environmental water-borne coating, and not only has good covering ability, but also will not cause film cracking under high and low-temperature environment; besides, it is toxic free and will not leave sharp smells after 3 working days so as to maintain good living quality.
It must be pointed out that the embodiments described above are only some embodiments of the present invention. All equivalent structures which employ the concepts disclosed in this specification and the appended claims should fall within the scope of the present invention.
Number | Date | Country | Kind |
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201710404022.8 | Jun 2017 | CN | national |