CN111826034A - Humidity-adjusting paint and method for producing the same - Google Patents
Humidity-adjusting paint and method for producing the same Download PDFInfo
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- CN111826034A CN111826034A CN201910310857.6A CN201910310857A CN111826034A CN 111826034 A CN111826034 A CN 111826034A CN 201910310857 A CN201910310857 A CN 201910310857A CN 111826034 A CN111826034 A CN 111826034A
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- XOJVVFBFDXDTEG-UHFFFAOYSA-N Norphytane Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 1
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- JCCZVLHHCNQSNM-UHFFFAOYSA-N [Na][Si] Chemical compound [Na][Si] JCCZVLHHCNQSNM-UHFFFAOYSA-N 0.000 description 1
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- POWFTOSLLWLEBN-UHFFFAOYSA-N tetrasodium;silicate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-] POWFTOSLLWLEBN-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Drying Of Gases (AREA)
- Paints Or Removers (AREA)
Abstract
Description
技术领域technical field
本发明涉及一种涂料配比及其制造方法,尤其涉及一调湿涂料及其制造方法。The invention relates to a paint ratio and a manufacturing method thereof, in particular to a humidity-controlling paint and a manufacturing method thereof.
背景技术Background technique
近年来湿气对室内环境所造成的影响,渐渐受到重视,相对湿度对环境居住者有直接的影响,例如过低的湿度,不仅会使居住者的呼吸系统产生干燥不舒适感,也是流行性感冒病毒活性大的湿度范围,容易使人感染生病,且低湿度也容易发生静电现象;反之,当过高的湿度容易在室内环境助长微生物及尘蹒等生物性污染孳生,如尘蹒容易存活于相对湿度50~80%之间,而湿度超过80%时,污染性微生物孳生机率将变大,这些生物性污染物都会间接造成居住者的不适,甚至引起呼吸器疾病、气喘、过敏、疲劳与头痛等健康上的问题。In recent years, the influence of humidity on the indoor environment has gradually been paid attention to. Relative humidity has a direct impact on the occupants of the environment. For example, too low humidity will not only make the occupant's respiratory system feel dry and uncomfortable, but also cause epidemics. The humidity range with high activity of cold virus is easy to make people infected and sick, and low humidity is also prone to static electricity; on the contrary, when the humidity is too high, it is easy to promote the growth of biological pollution such as microorganisms and dust mites in the indoor environment, and dust mites are easy to survive When the relative humidity is between 50 and 80%, and the humidity exceeds 80%, the probability of polluting microorganisms will increase. These biological pollutants will indirectly cause discomfort to the occupants, and even cause respiratory diseases, asthma, allergies, fatigue. Health problems such as headaches.
故住宅内部的湿度非常重要,而面对湿度问题,其主动方式主要是使用除湿剂、干燥剂、除湿机,或使用空调机等设备,此外,被动式部分,则着重用于建筑材料上的调湿材料,也有人研究可以调湿的涂料,而这些可以调湿的涂料主要采用沸石、海泡石或硅藻土之类的,还有人使用高分子吸水材料、矿物材料,如高岭土、硅土、石灰、铝矾土、砂石、水泥等添加植物纤维、农作物废弃物和活性碳等,且由调湿材料对吸放湿性能要求较高,很多的研究结果并没有能转换成产品流向市场,故选用何种材料,才能达到较佳的效益。Therefore, the humidity inside the house is very important. In the face of humidity problems, the active methods are mainly to use dehumidifiers, desiccants, dehumidifiers, or use equipment such as air conditioners. In addition, passive parts are mainly used for the adjustment of building materials. Wet materials, some people also study coatings that can adjust humidity, and these coatings that can adjust humidity mainly use zeolite, sepiolite or diatomaceous earth, and some people use polymer water-absorbing materials, mineral materials, such as kaolin, silica , lime, bauxite, gravel, cement, etc. are added with plant fibers, crop wastes and activated carbon, etc., and the moisture absorption and desorption performance of the moisture-conditioning materials is high, and many research results have not been converted into products to flow to the market. , so what kind of material is used can achieve better benefits.
此外,无机废弃物(如焚化灰渣、净水污泥、废硅藻土与煤灰等),每年在台湾的产生量极大,其回收利用率低,且成分以无机为主,无法使用焚化处理,故大部分会以掩埋的方式来处理,如此大量的废弃物进入掩埋场势必会加快掩埋场饱和的速度,若未有妥善掩埋,甚至会对生态环境造成严重的影响,故如果能将无机废弃物进行再利用作为资材,便可以达到资源循环社会的目的。In addition, inorganic wastes (such as incineration ash, water purification sludge, waste diatomite and coal ash, etc.) are produced in a large amount in Taiwan every year, and their recycling rate is low, and the components are mainly inorganic, which cannot be used. Incineration treatment, so most of them will be disposed of by burial. Such a large amount of waste entering the landfill will inevitably speed up the saturation of the landfill. If it is not properly buried, it will even have a serious impact on the ecological environment. Recycling inorganic waste as materials can achieve the goal of a resource recycling society.
发明内容SUMMARY OF THE INVENTION
因此,本发明的目的,是在提供一种调湿涂料及其制造方法,其能将废弃物转换成调湿涂料,有效降低废弃物对环境的影响外,同时也可以生产出调湿效果更佳的调湿涂料。Therefore, the purpose of the present invention is to provide a humidity-conditioning paint and a manufacturing method thereof, which can convert wastes into humidity-conditioning paints, effectively reduce the impact of wastes on the environment, and at the same time, can produce better humidity-conditioning effects. The best humidity control paint.
本发明第一目的在于提供一种调湿涂料,其包含有一30%重量百分比的功能材,一含有62.5~70%重量百分比的混合剂,以及一含有2.5%~7.5%重量百分比的硅酸钠;其中,该功能材包括有一20~60%重量百分比的无机泥渣,一35~65%的半水石膏,一至少5%重量百分比的无机矿物质,而上述该无机泥渣含有至少90%重量百分比的无晶型二氧化硅;另,该混合剂包含有水溶性树脂及水,而该水溶性树脂与该水的混合比例为1:(2~3)。The first object of the present invention is to provide a humidity control coating, which comprises a functional material of 30% by weight, a mixture containing 62.5% to 70% by weight, and a sodium silicate containing 2.5% to 7.5% by weight ; Wherein, the functional material includes a 20-60% by weight inorganic sludge, a 35-65% hemihydrate gypsum, an inorganic mineral at least 5% by weight, and the above-mentioned inorganic sludge contains at least 90% In addition, the mixture contains water-soluble resin and water, and the mixing ratio of the water-soluble resin and the water is 1:(2-3).
作为本发明的进一步改进,该水溶性树脂为丙烯酸树脂。As a further improvement of the present invention, the water-soluble resin is an acrylic resin.
作为本发明的进一步改进,该功能材中更可包含有10~30%重量比的石油炼化裂解废触媒。As a further improvement of the present invention, the functional material may further contain 10-30% by weight of the waste catalyst of petroleum refining and chemical cracking.
作为本发明的进一步改进,该无机泥渣经过烘干后,并研磨成粉末后,已通过#100号筛网所得之物。As a further improvement of the present invention, after the inorganic sludge has been dried and ground into powder, it has passed through the #100 sieve.
本发明第二目的在于提供一种调湿涂料,其包含有一30%重量百分比的功能材,一含有62.5~70%重量百分比的混合剂,以及一含有2.5%~7.5%重量百分比的硅酸钠;其中,该功能材包括有一20~60%重量百分比的无机泥渣,一35~65%的半水石膏,一至少5%重量百分比的无机矿物质,而上述该无机泥渣含有至少90%重量百分比的无晶型二氧化硅;另,该混合剂包含有水溶性油漆及水,而该水溶性油漆与该水的混合比例为1:(2~3)。The second object of the present invention is to provide a humidity-adjusting coating, which comprises a functional material of 30% by weight, a mixture containing 62.5% to 70% by weight, and a sodium silicate containing 2.5% to 7.5% by weight ; Wherein, the functional material includes a 20-60% by weight inorganic sludge, a 35-65% hemihydrate gypsum, an inorganic mineral at least 5% by weight, and the above-mentioned inorganic sludge contains at least 90% In addition, the mixture contains water-soluble paint and water, and the mixing ratio of the water-soluble paint and the water is 1:(2-3).
本发明第三目的在于提供一种调湿涂料的制造方法,其包含有:The 3rd object of the present invention is to provide a kind of manufacture method of humidity control paint, it comprises:
一备料步骤:其备有一含有30%重量百分比的功能材,一含有62.5~70%重量百分比的混合剂,以及一含有2.5%~7.5%重量百分比的硅酸钠;其中,该功能材包括有20~60%重量百分比的无机泥渣,35~65%重量百分比的半水石膏,以及至少5%重量百分比的无机矿物质,而上述该无机泥渣含有至少90%重量百分比的无晶型二氧化硅;另,该混合剂包含有一水溶性树脂及水,而该水溶性树脂与该水的混合比例为1:(2~3);及A material preparation step: it is equipped with a functional material containing 30% by weight, a mixture containing 62.5-70% by weight, and a sodium silicate containing 2.5%-7.5% by weight; wherein, the functional material includes: 20-60% by weight of inorganic sludge, 35-65% by weight of hemihydrate gypsum, and at least 5% by weight of inorganic minerals, and the above-mentioned inorganic sludge contains at least 90% by weight of amorphous II silicon oxide; in addition, the mixture contains a water-soluble resin and water, and the mixing ratio of the water-soluble resin and the water is 1:(2-3); and
一混合步骤:其分别先将属于固体混合物的功能材中拌合均匀,另该混合剂则先将该硅酸钠先与水搅拌混合成一硅酸钠溶液后,再将该水溶性树脂加入硅酸钠溶液搅拌均匀溶解后,再将该功能材与该混合剂进行混合搅拌,即完成该调湿涂料。A mixing step: firstly, the functional materials belonging to the solid mixture are mixed uniformly, and the other mixture is firstly mixed with the sodium silicate and water to form a sodium silicate solution, and then the water-soluble resin is added to the silicon After the sodium solution is stirred and dissolved evenly, the functional material and the mixture are mixed and stirred to complete the humidity control coating.
作为本发明的进一步改进,该水溶性树脂为丙烯酸树脂。As a further improvement of the present invention, the water-soluble resin is an acrylic resin.
作为本发明的进一步改进,该备料步骤中,更备具有2.5%~7.5%重量百分比的硅酸钠,且该硅酸钠先与水搅拌混合成一硅酸钠溶液后,再将该水溶性树脂加入硅酸钠溶液。As a further improvement of the present invention, in the material preparation step, sodium silicate with 2.5% to 7.5% by weight is further prepared, and the sodium silicate is first stirred and mixed with water to form a sodium silicate solution, and then the water-soluble resin Add sodium silicate solution.
作为本发明的进一步改进,该混合步骤中,于该混合剂调配时,先将该硅酸钠与水混合溶解形成一硅酸钠溶液后,再与该硅酸钠溶液中加入该水溶性树脂,并搅拌到该水溶性树脂完全溶解混合。As a further improvement of the present invention, in the mixing step, when the mixture is prepared, the sodium silicate is mixed and dissolved with water to form a sodium monosilicate solution, and then the water-soluble resin is added to the sodium silicate solution. , and stir until the water-soluble resin is completely dissolved and mixed.
作为本发明的进一步改进,该无机泥渣经过烘干后,并研磨成粉末后,以通过#100号筛网所得之物。As a further improvement of the present invention, the inorganic sludge is dried and ground into powder to pass through a #100 sieve.
与现有技术相比,本发明的有益效果在于:Compared with the prior art, the beneficial effects of the present invention are:
本发明利用该无机泥渣等主要废弃物所做成的调湿涂料,其能解决该无机泥渣掩埋的问题,有效将废弃物转换成高价值材料外,达到资源循环再利用的功效外,同时该调湿涂料也达到高吸放湿功效、高抗菌率等效果。The present invention uses the inorganic sludge and other main wastes to make the humidity-controlling paint, which can solve the problem of the inorganic sludge being buried, effectively convert the waste into high-value materials, and achieve the effect of resource recycling and reuse. At the same time, the humidity control coating also achieves the effects of high moisture absorption and desorption efficiency, high antibacterial rate and the like.
附图说明Description of drawings
图1为本发明一较佳实施例的制造流程图;1 is a manufacturing flow chart of a preferred embodiment of the present invention;
图2为本发明A组调湿涂层的孔径分析图;Fig. 2 is the pore size analysis diagram of A group humidity control coating of the present invention;
图3为本发明A组调湿涂层的湿度控制性能分析图;Fig. 3 is the humidity control performance analysis diagram of A group humidity control coating of the present invention;
图4为本发明A组吸附、解吸能力分析图;4 is an analysis diagram of the adsorption and desorption capacity of Group A of the present invention;
图5为本发明B组调湿涂层的孔径分析图;Fig. 5 is the pore size analysis diagram of the B group humidity control coating of the present invention;
图6为本发明B组调湿涂层的湿度控制性能分析图;Fig. 6 is the humidity control performance analysis diagram of the B group humidity control coating of the present invention;
图7为本发明B组吸附、解吸能力分析图;7 is an analysis diagram of the adsorption and desorption capacity of Group B of the present invention;
图8为本发明C组调湿涂层的孔径分析图;Fig. 8 is the pore size analysis diagram of C group humidity control coating of the present invention;
图9为本发明C组调湿涂层的湿度控制性能分析图;Fig. 9 is the humidity control performance analysis diagram of the C group humidity control coating of the present invention;
图10为本发明C组吸附、解吸能力分析图;Figure 10 is an analysis diagram of the C group adsorption and desorption capacity of the present invention;
图11为本发明水溶性油漆与水溶性树脂以相同混合比例的湿度控制性能分析图。Figure 11 is an analysis diagram of the humidity control performance of the water-soluble paint and water-soluble resin of the present invention in the same mixing ratio.
具体实施方式Detailed ways
有关本发明的上述及其他技术内容、特点与功效,在以下配合参考图式的较佳实施例的详细说明中,将可清楚的明白。The above and other technical contents, features and effects of the present invention will be clearly understood in the following detailed description of the preferred embodiments with reference to the drawings.
本发明第一较佳实施例,本实施例调湿涂料,其包含有一30%重量百分比的功能材,一含有62.5~70%重量百分比的混合剂,以及一含有2.5%~7.5%重量百分比的硅酸钠;其中,该功能材包括有一20~60%重量百分比的无机泥渣,一35~65%的半水石膏,以及一至少5%重量百分比的无机矿物质,而上述该无机泥渣含有至少90%重量百分比的无晶型二氧化硅;另,该混合剂包含有一水溶性树脂及水,而该水溶性树脂与该水的混合比例为1:(2~3),而上述该水溶性树脂(如为丙烯酸树脂),或者该水溶性黏合剂也可以使用水溶性油漆取代,而本实施例以下,该混合剂主要以水溶性树脂为例说明,而该水溶性树脂以丙烯酸树脂为例说明,以借助其黏性将该功能材料相互链接以进行涂抹;至于,该调湿涂料更包含有一2.5%~7.5%的硅酸钠;另外,该调湿涂料更可适时加入有一硅酸钠,且该硅酸钠占该调湿涂料2.5%~5%重量百分比。The first preferred embodiment of the present invention, the humidity-conditioning coating of this embodiment, comprises a functional material of 30% by weight, a mixture containing 62.5% to 70% by weight, and a mixture of 2.5% to 7.5% by weight Sodium silicate; wherein, the functional material includes a 20-60% by weight inorganic sludge, a 35-65% hemihydrate gypsum, and an inorganic mineral at least 5% by weight, and the above-mentioned inorganic sludge Contains at least 90% by weight of amorphous silica; in addition, the mixture contains a water-soluble resin and water, and the mixing ratio of the water-soluble resin and the water is 1: (2-3), and the above-mentioned Water-soluble resin (such as acrylic resin), or the water-soluble adhesive can also be replaced by water-soluble paint, and below this embodiment, the mixture is mainly described by taking water-soluble resin as an example, and the water-soluble resin is acrylic resin. As an example, the functional materials are linked to each other for painting by virtue of their viscosity; as for the humidity-conditioning coating, the humidity-conditioning coating further contains a sodium silicate of 2.5% to 7.5%; in addition, the humidity-conditioning coating can also be added in a timely manner. A silicon Sodium, and the sodium silicate accounts for 2.5% to 5% by weight of the humidity control coating.
仍续上述,该无机泥渣ESF(Enhancement Silica Fume)是来自传统工业的无机污泥,是台湾沈淀二氧化硅的生产商,将该无机泥渣经过烘干后,并研磨成粉末以通过0.149mm筛(即#100号筛网所得之物),而本发明中以该无机泥渣以在105℃下通过空气循环烘箱干燥48小时后,冷却至室温后再进行研磨所得之物,而该无机泥渣可挑选化学组成以无晶型二氧化硅为主,且该无晶型二氧化硅含量为至少90%重量百分比以上;此外,该无机泥渣是一种具有微尺寸颗粒的无定形二氧化硅,可以完全悬浮在水中,SiO2(在25℃下在水中0.01至0.012重量百分比)的溶解产生单体形式(即Si(OH)4和固相无机泥碴分散在溶剂中,其可以用树脂粘附,并在石膏棒状颗粒的交联结构之间固结,而形成中孔与微孔结构由无机泥渣和石膏形成,加入该无机泥渣可以为调湿涂层结构提供更多的介孔,然而过量的无机泥渣会使调湿涂层表面龟裂,因此必须控制该无机泥渣的添加量。Continuing the above, the inorganic sludge ESF (Enhancement Silica Fume) is an inorganic sludge from traditional industries, which is a manufacturer of precipitated silica in Taiwan. After drying, the inorganic sludge is ground into powder to pass 0.149mm sieve (that is, the thing obtained from the #100 sieve), and in the present invention, the inorganic sludge is dried in an air circulation oven at 105 ° C for 48 hours, cooled to room temperature, and then ground is obtained, and The chemical composition of the inorganic sludge can be selected to be mainly amorphous silica, and the content of the amorphous silica is at least 90% by weight; Shaped silica, which can be completely suspended in water, dissolution of SiO2 (0.01 to 0.012 weight percent in water at 25°C) yields a monomeric form (i.e. Si(OH) 4 and solid-phase inorganic sludge dispersed in a solvent, It can be adhered with resin and consolidated between the cross-linked structure of gypsum rod-like particles, and the mesoporous and microporous structure is formed by inorganic sludge and gypsum, and the addition of this inorganic sludge can provide moisture-conditioning coating structure. More mesopores, however, excessive inorganic sludge will crack the surface of the humidity-conditioning coating, so the addition amount of the inorganic sludge must be controlled.
仍续上述,该无机矿物质可为重晶石、高岭土、滑石和石灰石的其一或其混合,而该无机矿物质作为一增量剂,以改善涂料的机械性能以及涂料膜的光泽度,渗透性和流平性,该增量剂不溶于黏合剂和混合剂,故该无机矿物质比例通常不超过25%;另外,更可于该功能材中适时加入有10~30%重量比的石油炼化裂解废触媒(sFCCC)。Continuing the above, the inorganic mineral can be one of barite, kaolin, talc and limestone or a mixture thereof, and the inorganic mineral acts as an extender to improve the mechanical properties of the coating and the gloss of the coating film, Permeability and leveling, the extender is insoluble in binders and admixtures, so the proportion of inorganic minerals is usually not more than 25%; in addition, 10-30% by weight can be added to the functional material. Petroleum refining cracking waste catalyst (sFCCC).
参阅图1,该调湿涂料制造方法,其依序包含有备料步骤、混合步骤;其中,该备料步骤其备有一30%重量百分比的功能材以及62.5~70%重量百分比的混合剂;其中,该功能材包括有20~60%重量百分比的无机泥渣,35~65%重量百分比的半水石膏,以及至少5%重量百分比的无机矿物质,而上述该无机泥渣含有至少90%重量百分比的无晶型二氧化硅;另,该混合剂包含有一水溶性树脂及水,而该水溶性树脂与该水的混合比例为1:(2~3),而混合剂从该水溶性树脂改用成水溶性油漆时,仍可采取相同的制造方法,而本实施例以下以水溶性树脂为例说明,且该水溶性树脂是采用丙烯酸树脂为实验说明;另,该混合步骤其分别先将属于固体混合物的功能材中的无机泥渣、半水石膏及无机矿物质拌合均匀,以及属于液态状的混合剂中的丙烯酸树脂及水搅拌均匀后,再将该功能材与该混合剂进行混合搅拌,即完成该调湿涂料;此外,如果有加入2.5%~7.5%重量百分比的硅酸钠,且该硅酸钠先与水搅拌混合成一硅酸钠溶液后,再将该丙烯酸树脂加入硅酸钠溶液。Referring to FIG. 1, the manufacturing method of the humidity-controlling coating includes a material preparation step and a mixing step in sequence; wherein, the material preparation step includes a functional material of 30% by weight and a mixture of 62.5 to 70% by weight; wherein, The functional material includes 20-60% by weight of inorganic sludge, 35-65% by weight of hemihydrate gypsum, and at least 5% by weight of inorganic minerals, and the inorganic sludge contains at least 90% by weight of In addition, the mixture contains a water-soluble resin and water, and the mixing ratio of the water-soluble resin and the water is 1:(2~3), and the mixture is changed from the water-soluble resin. When used as a water-soluble paint, the same manufacturing method can still be adopted, and the water-soluble resin is used as an example for illustration in this embodiment, and the water-soluble resin is an experimental illustration by using an acrylic resin; The inorganic sludge, hemihydrate gypsum and inorganic minerals in the functional material belonging to the solid mixture are evenly mixed, and the acrylic resin and water in the liquid mixture are evenly mixed, and then the functional material is mixed with the mixture. Mix and stir to complete the humidity control coating; in addition, if 2.5% to 7.5% by weight of sodium silicate is added, and the sodium silicate is first stirred and mixed with water to form a sodium silicate solution, then the acrylic resin is added to the Sodium silicate solution.
表一、本实施例中,将列出以下列出几种实验例,而本实施例中混合剂中的水溶性树脂:去离子水配比以1:2.5为例说明,并分别制作出多组配比,以证明本发明调湿涂料具有一定的功效:Table 1. In this example, several experimental examples will be listed below, and the water-soluble resin in the mixture in this example: the ratio of deionized water is 1:2.5 as an example to illustrate, and respectively make more The composition ratio is to prove that the humidity-controlling paint of the present invention has a certain effect:
表一,本发明所举例的实验例配比:Table 1, the ratio of the experimental example exemplified in the present invention:
以上制作完成的配比,将上述所制作而成的调湿涂料,以样本大小100mm*100mm,厚度为2mm,遵循JIS-A 1470的规格,水分吸附-解吸试验。在25℃下在75%RH(Relativehumidity,相对湿度)下固化24小时后,然后放置在室内环境2天进行测试,以下针对A组为调整无机泥渣添加配比、B组为调整硅酸钠添加配比、C组为调整废触媒添加配比,以形成一调湿涂层作为后续实验对象,以及对该无机泥渣、硅酸钠及废触媒添加量多寡影响该调湿涂层特性进行说明。For the above prepared proportions, the moisture-adjusting paint prepared above was tested with a sample size of 100mm*100mm and a thickness of 2mm, following the specifications of JIS-A 1470, and the moisture adsorption-desorption test. After curing at 25°C under 75%RH (Relativehumidity, relative humidity) for 24 hours, it was then placed in an indoor environment for 2 days for testing. The following is for group A to adjust the addition ratio of inorganic sludge, and group B to adjust the sodium silicate The addition ratio, group C is to adjust the addition ratio of the waste catalyst to form a humidity-conditioning coating as the follow-up experimental object, and the addition of the inorganic sludge, sodium silicate and waste catalyst affects the properties of the humidity-conditioning coating. illustrate.
首先针对以下针对A组有关添加无机泥渣多寡进行测试,以不同无机泥渣配比所产生的调湿涂层对于多孔性质的变化,其如下表中所示:First of all, the following tests are carried out on the amount of inorganic sludge added to Group A, and the changes in the porous properties of the humidity-conditioning coating produced by different inorganic sludge ratios are shown in the following table:
表二,添加有不同无机泥渣配比所产生的调湿涂层多孔性质:Table 2, the porous properties of the humidity-conditioning coating produced by adding different ratios of inorganic sludge:
如上表所述,对于具有不同无机泥渣添加量所形成的调湿涂层,随着无机泥渣比率增加,调湿涂层BET表面积(Brunauer-Emmet-Teller)和总孔体积增加,测得具有不同无机泥渣比(A-0.4/0.05/0,A-0.5/0.05/0和A-0.6/0.05/0)的调湿涂层的BET表面积分别为10.01m2/g、13.1m2/g、13.5m2/g,皆比原始未添加有无机泥渣的试验组A-0/0.05/0所得3.9m2/g增加;随着无机泥渣增加,总孔体积也增加,从原本的0.049cm3/g,增加至0.206cm3/g,因此,皆能证明添加无机泥渣可以增强孔体积和BET表面积;再者,无机泥渣中的中孔(2nm~50nm)是最有效的水分吸附孔,因此,添加有该无机泥渣时,将可有效增加中孔的体积,如图2调湿涂层的孔径分布所证明。As described in the above table, for the humidity-conditioning coatings formed with different amounts of inorganic sludge added, as the ratio of inorganic sludge increases, the BET surface area (Brunauer-Emmet-Teller) and total pore volume of the humidity-conditioning coating increase, measured as The BET surface areas of the humidity-conditioning coatings with different inorganic sludge ratios (A-0.4/0.05/0, A-0.5/0.05/0 and A-0.6/0.05/0) were 10.01 m 2 /g, 13.1 m 2 , respectively /g, 13.5m 2 /g, both increased compared with 3.9m 2 /g obtained in the original test group A-0/0.05/0 without inorganic sludge added; with the increase of inorganic sludge, the total pore volume also increased, from The original 0.049cm 3 /g was increased to 0.206cm 3 /g. Therefore, it can be proved that the addition of inorganic sludge can enhance the pore volume and BET surface area. Furthermore, the mesopores (2nm-50nm) in the inorganic sludge are the most Effective moisture adsorption pores, therefore, when the inorganic sludge is added, the volume of mesopores can be effectively increased, as evidenced by the pore size distribution of the humidity-conditioning coating in Figure 2.
仍续上述,参阅表三,水分吸附值和水分含量Continuing above, see Table 3, Moisture Adsorption Value and Moisture Content
如表三所示,根据JIS-A 6909(从50%RH至90%RH)的方法,具有不同无机泥渣比率的调湿涂层的水分吸附容量示于表中,水分吸附值和水分含量A-0/0.05/0分别为216.9g/m2和16.3%,故可以看出,随着无机泥渣的量增加,调湿涂层水分吸附容量逐渐增加,即具有无机泥渣的样品的性能优于不具无机泥渣A-0/0.05/0的样品;结果显示A-0.4/0.05/0,A-0.5/0.05/0和A-0.6/0.05/0)的容量可以达到270.3g/m2,303.7g/m2和316.1g/m2,分别;此外,A-0.4/0.05/0,A-0.5/0.05/0和A-0.6/0.05/0的水分含量分别为23.6%,25.6%和26.7%,其能证明吸湿能力与BET表面积和总孔体积呈正相关。As shown in Table 3, according to the method of JIS-A 6909 (from 50% RH to 90% RH), the moisture adsorption capacity of the humidity-conditioning coatings with different inorganic sludge ratios is shown in the table, the moisture adsorption value and the moisture content A-0/0.05/0 are 216.9 g/m 2 and 16.3%, respectively, so it can be seen that with the increase in the amount of inorganic sludge, the moisture adsorption capacity of the humidity-conditioning coating gradually increases, that is, the sample with inorganic sludge increases. The performance is better than the sample without inorganic sludge A-0/0.05/0; the results show that the capacity of A-0.4/0.05/0, A-0.5/0.05/0 and A-0.6/0.05/0) can reach 270.3g/ m 2 , 303.7 g/m 2 and 316.1 g/m 2 , respectively; in addition, the moisture contents of A-0.4/0.05/0, A-0.5/0.05/0 and A-0.6/0.05/0 were 23.6%, respectively, 25.6% and 26.7%, which can demonstrate that the hygroscopic capacity is positively correlated with BET surface area and total pore volume.
再者,通过水分吸附-解吸试验(JIS-A 1470-1)在中等湿度范围(50%RH-75%RH)下测量不同无机泥渣比例对调湿涂层的湿度控制性能,其相应的结果如图3所示,除A-0/0.05/0样品外,A-0.4/0.05/0,A-0.5/0.05/0和A-0.6/0.05/0在中等湿度范围内具有较高的水分吸附能力,表示无机泥渣具有对水分吸附有积极作用;另外,湿度控制材料(1级和2级)的标准吸附容量为29g/m2,吸附时间为12h,为50g/m2;A-0.4/0.05/0,A-0.5/0.05/0和A-0.6/0.05/0样品的水分吸附容量分别为48.6g/m2,88.4g/m2和46.1g/m2,吸附时间为12h,达到1级基准,接近2级;各种样品的吸附-解吸梯度为A-0.5/0.05/0样品的吸附率最高(20.1g/m2/h);此外,对于A-0.4/0.05/0(-17.3g/m2/h),可以观察到最佳解吸速率;结果表明,含有无机泥渣的调湿涂层吸附和解吸速率快于不含无机泥渣的调湿涂层,故本发明实验证明,通过加入该无机泥渣确实可得到一定调湿功效。Furthermore, the humidity control performance of the humidity-conditioning coating with different proportions of inorganic sludge was measured by the moisture adsorption-desorption test (JIS-A 1470-1) under the medium humidity range (50%RH-75%RH), and the corresponding results As shown in Figure 3, except for the A-0/0.05/0 sample, A-0.4/0.05/0, A-0.5/0.05/0 and A-0.6/0.05/0 had higher moisture in the medium humidity range Adsorption capacity, indicating that the inorganic sludge has a positive effect on moisture adsorption; in addition, the standard adsorption capacity of the humidity control material (grade 1 and grade 2) is 29g/m 2 , and the adsorption time is 12h, which is 50g/m 2 ; A- The moisture adsorption capacities of the 0.4/0.05/0, A-0.5/0.05/0 and A-0.6/0.05/0 samples were 48.6 g/m 2 , 88.4 g/m 2 and 46.1 g/m 2 , respectively, and the adsorption time was 12 h , reaching the level 1 benchmark, which is close to level 2; the adsorption-desorption gradient of various samples is A-0.5/0.05/0 sample has the highest adsorption rate (20.1g/m 2 /h); in addition, for A-0.4/0.05/ 0 (-17.3g/m 2 /h), the best desorption rate can be observed; the results show that the adsorption and desorption rate of the humidity-conditioning coating containing inorganic sludge is faster than that of the humidity-conditioning coating without inorganic sludge, so The experiment of the present invention proves that certain humidity control effect can indeed be obtained by adding the inorganic sludge.
另外,以下将针对B组有关硅酸钠在调湿涂层中的作用进行实验组进行说明,即针对B-0.5/0/0、B-0.5/0.025/0、B-0.5/0.5/0、B-0.5/0.075/0及等实验例进行说明,即针对不同硅酸钠比例的调湿涂层的多孔性质,如下表四:In addition, the following will describe the experimental group for the effect of sodium silicate in the humidity control coating of group B, that is, for B-0.5/0/0, B-0.5/0.025/0, B-0.5/0.5/0 , B-0.5/0.075/0 and other experimental examples are described, that is, the porous properties of the humidity-conditioning coatings with different ratios of sodium silicate are shown in Table 4 below:
表四,添加有不同硅酸钠比例所产生的调湿涂层多孔性质:Table 4. Porous properties of humidity-conditioning coatings with different ratios of sodium silicate added:
测得不同比例的硅酸钠(B-0.5/0/0,B-0.5/0.025/0,B-0.5/0.05/0和B-0.5/0.075/0)的调湿涂层的BET表面积分别为16.18m2/g,13.28m2/g,13.1m2/g和11.52m2/g,调湿涂层B样品的总孔体积也增加(B-0.5/0/0=0.190cm3/g,B-0.5/0.025/0=0.167cm3/g,B-0.5/0.05/0=0.193cm3/g和B-0.5/0.075/0=0.126cm3/g);因此,随着硅酸钠的增加,观察到BET表面积和孔体积的减小趋势;然而,随着硅酸钠的量增加,微孔面积和微孔体积增加,这是由于从孔中的硅酸填充小二氧化硅颗粒(单体)和硅酸盐的聚合引起的,中孔的体积几乎没有变化,这可以图4孔径分布中看出,同时几乎观察不到B-0.5/0.075/0的较大孔;另外,经过实验,B-0.5/0/0的水滴吸附时间为34秒,B-0.5/0.025/0的水滴吸附时间为69秒、B-0.5/0.05/0的水滴吸附时间为67秒,而B-0.5/0.075/0的水滴吸附时间为79秒,显示含有不同量硅酸钠的调湿涂层需要更长的时间进行吸附,这些结果表明,含有硅酸钠的调湿涂层可以比原始调湿涂层更慢地吸附液态水,这可能是由于硅酸形成小的二氧化硅颗粒和硅酸盐的聚合。The BET surface areas of the humidity-conditioning coatings with different ratios of sodium silicate (B-0.5/0/0, B-0.5/0.025/0, B-0.5/0.05/0 and B-0.5/0.075/0) were measured, respectively. At 16.18 m 2 /g, 13.28 m 2 /g, 13.1 m 2 /g and 11.52 m 2 /g, the total pore volume of the humidity-conditioning coating B samples also increased (B-0.5/0/0=0.190 cm 3 / g, B-0.5/0.025/0=0.167 cm 3 /g, B-0.5/0.05/0=0.193 cm 3 / g and B-0.5/0.075/0=0.126 cm 3 /g); therefore, with silicon With the increase of sodium silicate, a decreasing trend of BET surface area and pore volume was observed; however, as the amount of sodium silicate increased, the micropore area and micropore volume increased due to the filling of small dioxide from silicic acid in the pores The volume of mesopores is almost unchanged due to the polymerization of silicon particles (monomers) and silicates, which can be seen in the pore size distribution in Fig. 4, while the larger pores of B-0.5/0.075/0 are hardly observed; In addition, after experiments, the water droplet adsorption time of B-0.5/0/0 was 34 seconds, the water droplet adsorption time of B-0.5/0.025/0 was 69 seconds, and the water droplet adsorption time of B-0.5/0.05/0 was 67 seconds. The water droplet adsorption time of B-0.5/0.075/0 was 79 seconds, which showed that the humidity-conditioning coatings containing different amounts of sodium silicate needed longer time for adsorption. These results indicated that the humidity-conditioning coatings containing sodium silicate could Absorbs liquid water more slowly than pristine humidity-conditioning coatings, possibly due to silicic acid forming small silica particles and polymerization of silicates.
再者,参阅表五,含有不同重量比硅酸钠的调湿涂层的吸湿能力:Furthermore, referring to Table 5, the moisture absorption capacity of the moisture-conditioning coatings containing different weight ratios of sodium silicate:
随着硅酸钠比例的增加,水分吸附值和水分含量增加,如表五所示,该调湿涂层与硅酸钠的水分吸附值为B-0.5/0.025/0=225.6g/m2,B-0.5/0.05/0=303.7g/m2,B-0.5/0.075/0=410.2g/m2,分别大于B-0.5/0/0(吸湿值=72.7g/m2)。此外,B-0.5/0/0,B-0.5/0.025/0,B-0.5/0.05/0和B-0.5/0.075/0的含水量分别为5.4%,18.8%,25.6%和28.8%;另外,调湿涂层B的湿度控制性能如图5所示(在中等湿度范围(50%RH至75%RH)下进行);具有不同硅酸钠比例的在低湿度范围内对水分存储容量存在显着差异,表明硅酸钠对水分吸附具有积极作用。B-0.5/0.075/0样品在12小时时具有68.1g/m2,达到2级基准并接近3级,所有调湿涂层均可达到1级的最低标准;此外,B-0.5/0.075/0样品显示出最佳吸附速率(20.8g/m2/h),并且根据图6中的吸附-解吸梯度,具有最佳解吸率(-17.6g/m2/h),另外随着硅酸钠比例的增加,调湿涂层中水分吸附的响应速率更快;此外,解吸过程中水分吸附能力的持久性保持稳定,此外,在四次循环试验后不会发生水分含量的累积,其通过硅酸钠存在下(由于化学吸附),水分吸附能力显着提高,并且陶瓷涂料的稳定性更佳。As the proportion of sodium silicate increases, the moisture adsorption value and moisture content increase. As shown in Table 5, the moisture adsorption value of the humidity-adjusting coating and sodium silicate is B-0.5/0.025/0=225.6g/ m2 , B-0.5/0.05/0=303.7g/m 2 , B-0.5/0.075/0=410.2g/m 2 , which are respectively greater than B-0.5/0/0 (moisture absorption value=72.7g/m 2 ). In addition, the water contents of B-0.5/0/0, B-0.5/0.025/0, B-0.5/0.05/0 and B-0.5/0.075/0 were 5.4%, 18.8%, 25.6% and 28.8%, respectively; In addition, the humidity control performance of the humidity-conditioning coating B is shown in Fig. 5 (performed in the medium humidity range (50%RH to 75%RH)); the moisture storage capacity in the low humidity range with different ratios of sodium silicate There are significant differences, indicating that sodium silicate has a positive effect on moisture adsorption. The B-0.5/0.075/0 sample had 68.1 g/m 2 at 12 hours, reaching the
最后,将针对C组有关废触媒(sFCCCs)在调湿涂层中的作用进行实验组进行说明,硅酸钠是湿度控制涂料的添加剂,其SiO2/Na2O比为2.05~2.25在先前的研究中确定了无机泥渣和硅酸钠的最佳比例,对于具有不同无机泥渣比率的调湿涂层,水分吸附值在中等湿度范围内不会受到显着影响;而当使用废触媒来替代无机泥渣的一部分,由于沸石结构的存在,其改善了孔径的分布;然而,由于较大的废触媒颗粒及添加过量的废触媒会降低涂层的黏度,而先对于添加有该废触媒所造成的孔径分布如下表六:Finally, the experimental group on the role of spent catalysts ( sFCCCs ) in humidity control coatings in group C will be explained. Sodium silicate is an additive for humidity control coatings. The optimum ratio of inorganic sludge and sodium silicate was determined in the study of , for humidity-conditioning coatings with different ratios of inorganic sludge, the moisture adsorption value was not significantly affected in the medium humidity range; To replace part of the inorganic sludge, due to the existence of the zeolite structure, it improves the pore size distribution; however, due to the larger waste catalyst particles and the addition of excess waste catalyst will reduce the viscosity of the coating, and the addition of the waste catalyst will reduce the viscosity of the coating first. The pore size distribution caused by the catalyst is shown in Table 6 below:
表六 为不同比例的废触媒替代物的调湿涂层的多孔性质:Table 6 shows the porous properties of humidity-conditioning coatings with different ratios of spent catalyst substitutes:
由于沸石结构,废触媒具有高BET表面积(129m2/g)和丰富的微孔性质,在微孔存在下可以增强水分吸附的能力,调湿涂层使用不同比例的废触媒替代时,其BET表面积(C-0.4/0.05/0.1,C-0.3/0.05/0.2和C-0.2/0.05/0.3)为16.8m2/g,14.7m2/g和13.3m2/g,分别大于原始C-0.5/0.05/0(13.1m2/g),如表六所示,此外,替换废触媒的调湿涂层的平均孔径较小(约30nm),此外,发现t-型微孔面积和体积增加;参阅图7,其孔径显示较小的尺寸分布(小于25nm),在较低的相对湿度下更有效,在C-0.4/0.05/0.1样品在中孔(2至50nm)中具有最佳分布,由于通过替换废触媒减少的无机泥渣的含量,孔体积在25至50nm的范围内逐渐降低;另外,经过测试,随着废触媒替代率的增加,会使得调湿涂层的吸附时间增加,发现C-0.3/0.05/0.2和C-0.2/0.05/0.3在130秒的时间内几乎不吸附水滴,C-0.3/0.05/0.2和C-0.2/0.05/0.3的表面接触角分别在35秒时为35.58°和45.8°,这是由于较大孔的减少,废触媒具有很强的吸附水蒸气的能力和弱的液体水吸附能力;因此,上述结果表明,废触媒对微孔具有正面影响,但对调湿涂层的较大孔具有负面影响。Due to the zeolite structure, the waste catalyst has a high BET surface area (129m 2 /g) and abundant microporous properties, which can enhance the ability of moisture adsorption in the presence of micropores. When the humidity-conditioning coating is replaced with different proportions of waste catalyst, its BET The surface areas (C-0.4/0.05/0.1, C-0.3/0.05/0.2 and C-0.2/0.05/0.3) were 16.8 m 2 /g, 14.7 m 2 /g and 13.3 m 2 /g, respectively, larger than the original C- 0.5/0.05/0 (13.1 m 2 /g), as shown in Table 6, in addition, the average pore size of the humidity-conditioning coating that replaced the spent catalyst was smaller (about 30 nm), and in addition, it was found that the area and volume of t-type micropores increase; see Figure 7, its pore size shows a smaller size distribution (less than 25 nm), is more efficient at lower relative humidity, with the best C-0.4/0.05/0.1 sample in mesopores (2 to 50 nm) distribution, the pore volume gradually decreases in the range of 25 to 50 nm due to the content of inorganic sludge reduced by replacing the spent catalyst; in addition, after testing, with the increase of the replacement rate of the spent catalyst, the adsorption time of the humidity-conditioning coating will be reduced. increase, it was found that C-0.3/0.05/0.2 and C-0.2/0.05/0.3 hardly adsorbed water droplets within 130 seconds, and the surface contact angles of C-0.3/0.05/0.2 and C-0.2/0.05/0.3 were in 35.58° and 45.8° at 35 seconds, which is due to the reduction of larger pores, and the waste catalyst has a strong ability to adsorb water vapor and a weak liquid water adsorption capacity; therefore, the above results show that the waste catalyst has a strong ability to adsorb micropores. A positive effect, but a negative effect on the larger pores of the humidity-conditioning coating.
再者,参阅表七,含有不同重量比硅酸钠的调湿涂层的吸湿能力;另外,具有废触媒的调湿涂料的水分吸附值和梯度的结果,参阅图8、图9,C-0.2/0.05/0.3样品的水分吸附值最高,为71.6g/m2,达到3级基准;对于C-0.4/0.05/0.1和C-0.3/0.05/0.2样品,水分吸附值分别为56.9g/m2和59.5g/m2,达到2级基准,此外,水分吸附-解吸梯度具有相似的趋势;其中的C-0.5/0.05/0吸湿值为48.4g/m2,吸附解吸梯度分别为20.1g/m2/h和-16g/m2/h,其中,C-0.2/0.05/0.3具有优异的吸附梯度(20.3g/m2/h)和解吸梯度(-24.4g/m2/h);根据结果,可以看出,随着废触媒替代率的增加,在中等湿度范围内吸附能力得到改善。Furthermore, referring to Table 7, the moisture absorption capacity of the humidity-conditioning coatings containing different weight ratios of sodium silicate; in addition, the results of the moisture absorption values and gradients of the humidity-conditioning coatings with waste catalysts, see Fig. 8, Fig. 9, C- The 0.2/0.05/0.3 sample has the highest moisture adsorption value of 71.6g/m 2 , reaching the
表七:含有不同重量比废触媒的调湿涂层的吸湿能力:Table 7: Moisture absorption capacity of humidity-conditioning coatings with different weight ratios of waste catalysts:
另外,本实验例中,本实施例中以JIS-A-1470-1方法进行最佳的配比如下表八,在上述比例的下,其中的水溶性树脂(丙烯酸树脂)与水溶性油漆进行比较:In addition, in this experimental example, in this example, the best ratio is carried out by the method of JIS-A-1470-1 as the following table 8. Under the above ratio, the water-soluble resin (acrylic resin) and the water-soluble paint are mixed with Compare:
表八:本实验例水溶性树脂与水溶性油漆同时采用的配比:Table 8: The ratio of water-soluble resin and water-soluble paint used in this experimental example at the same time:
其结果如图11所示,发现其吸附效果也很好,水溶性油漆的水分吸附值达52.57g/m2,而水溶性树脂为57.25g/m2,皆达到第二级的效果,因此,该混合剂中的水溶性树脂(丙烯酸树脂)改用为水溶性油漆时,其仍可达到不错的效果。The results are shown in Figure 11. It is found that the adsorption effect is also very good. The water adsorption value of the water-soluble paint is 52.57g/m 2 and the water-soluble resin is 57.25g/m 2 , both of which reach the second-level effect. Therefore, , when the water-soluble resin (acrylic resin) in the mixture is changed to water-soluble paint, it can still achieve a good effect.
再者,根据JIS-A 6909(从50%RH至90%RH)的方法,以上述测试的配比做为测试,调湿涂层的水分吸附容量示于表九中,水溶性油漆水分吸附值和水分含量分别为316.8g/m2和25.1%,而水溶性树脂水分吸附值和水分含量分别为309.2g/m2和27.6%,故可看出将混和剂配方做调整,以水溶性油漆替代水溶性树脂,效果仍优异。Furthermore, according to the method of JIS-A 6909 (from 50% RH to 90% RH), the ratio of the above test is used as a test, and the moisture adsorption capacity of the humidity-conditioning coating is shown in Table 9. The water-soluble paint moisture adsorption capacity Value and moisture content are 316.8g/m 2 and 25.1% respectively, while the water adsorption value and moisture content of water-soluble resin are 309.2g/m 2 and 27.6% respectively, so it can be seen that the formula of the mixture is adjusted to make the water-soluble resin more suitable The paint replaces the water-soluble resin, and the effect is still excellent.
表九:水溶性油漆及水溶性树脂于高湿度时的吸湿能力Table 9: Moisture absorption capacity of water-soluble paint and water-soluble resin at high humidity
另外,以抗菌功能进行测试而言,以JIS Z 2801:2010标准方法测定,如表十中所示:In addition, in terms of testing the antibacterial function, it is determined by the standard method of JIS Z 2801:2010, as shown in Table 10:
表十:抗菌活性测试Table 10: Antibacterial activity test
仍续上述,由表十,经抗菌功能测试后,抗菌活性(R因子)的值比2.87高4.78,这是JIS Z 2801:2010标准方法中的阈值,该结果表明本发明调湿涂层确实具有抗微生物功效高于99.99%的功效。Continuing the above, from Table 10, after the antibacterial function test, the value of antibacterial activity (R factor) is 4.78 higher than 2.87, which is the threshold value in the standard method of JIS Z 2801:2010, and the result shows that the humidity-conditioning coating of the present invention is indeed Has antimicrobial efficacy higher than 99.99%.
归纳上述,本发明调湿涂料及其制造方法,该调湿涂料包含有一30%重量百分比的功能材,一含有62.5~70%重量百分比的混合剂,以及一含有2.5%~7.5%重量百分比的硅酸钠;即为通过一定比例的无机泥渣、半水石膏及无机矿物质、硅酸钠、水、及水溶性树脂混合调配出该调湿涂料,且调配后的调湿涂料具有高吸、放湿功效、高抗菌率外,同时也解决了无机泥渣掩埋的问题,有效将废弃物转换成高价值材料,有效达到资源循环再利用的功效,故的确可达到本发明的目的。To sum up the above, the humidity-conditioning coating and the manufacturing method thereof of the present invention, the humidity-conditioning coating comprises a functional material of 30% by weight, a mixture containing 62.5-70% by weight, and a compound containing 2.5%-7.5% by weight Sodium silicate; that is, the humidity-conditioning coating is prepared by mixing a certain proportion of inorganic sludge, hemihydrate gypsum and inorganic minerals, sodium silicate, water, and water-soluble resin, and the prepared humidity-conditioning coating has high absorption In addition to the effect of dehumidification and high antibacterial rate, it also solves the problem of inorganic sludge burial, effectively converts waste into high-value materials, and effectively achieves the effect of resource recycling, so it can indeed achieve the purpose of the present invention.
以上仅为本发明的优选实施例而已,并不用于限制本发明,对于本领域的技术人员来说,本发明可以有各种更改和变化。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。The above are only preferred embodiments of the present invention, and are not intended to limit the present invention. For those skilled in the art, the present invention may have various modifications and changes. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention shall be included within the protection scope of the present invention.
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW432024B (en) * | 1998-01-23 | 2001-05-01 | Formosa Petrochemical Corp | Process of adding waste FCC catalysts into concrete |
US20030056694A1 (en) * | 2001-09-25 | 2003-03-27 | Macklin Michael B. | Pumpably verifiable fluid fiber compositions |
CN102888155A (en) * | 2012-10-26 | 2013-01-23 | 合众(佛山)化工有限公司 | Preparation method of odorless environment-friendly humidifying antibacterial paint |
CN105130362A (en) * | 2015-07-21 | 2015-12-09 | 汪涛涛 | Humidity-regulating light-weight calcium silicate board and production method thereof |
CN106163640A (en) * | 2014-04-14 | 2016-11-23 | 富士胶片株式会社 | Hygroscopic material and manufacture method thereof and blister package |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW432024B (en) * | 1998-01-23 | 2001-05-01 | Formosa Petrochemical Corp | Process of adding waste FCC catalysts into concrete |
US20030056694A1 (en) * | 2001-09-25 | 2003-03-27 | Macklin Michael B. | Pumpably verifiable fluid fiber compositions |
CN102888155A (en) * | 2012-10-26 | 2013-01-23 | 合众(佛山)化工有限公司 | Preparation method of odorless environment-friendly humidifying antibacterial paint |
CN106163640A (en) * | 2014-04-14 | 2016-11-23 | 富士胶片株式会社 | Hygroscopic material and manufacture method thereof and blister package |
CN105130362A (en) * | 2015-07-21 | 2015-12-09 | 汪涛涛 | Humidity-regulating light-weight calcium silicate board and production method thereof |
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