TW467943B - Photocatalytically hydrophilifiable coating composition - Google Patents

Photocatalytically hydrophilifiable coating composition Download PDF

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TW467943B
TW467943B TW86110219A TW86110219A TW467943B TW 467943 B TW467943 B TW 467943B TW 86110219 A TW86110219 A TW 86110219A TW 86110219 A TW86110219 A TW 86110219A TW 467943 B TW467943 B TW 467943B
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Taiwan
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composition
patent application
scope
item
coating
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TW86110219A
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Chinese (zh)
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Makoto Hayakawa
Mitsuyoshi Kanno
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Toto Ltd
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Abstract

A composition is disclosed which can hydrophilify the surface of a member to impart an antifogging property to the surface of the member. The composition for hydrophilifying the surface of the member comprises at least (a) photocatalytic particles of a metallic oxide, (b) a precursor capable of forming a silicone resin film or a precursor capable of forming a silica film, and (c) a solvent, the total content of the photocatalytic particle and the solid matter of the precursor in the composition being 0.01 to 5% by weight. The hydrophilic property can be imparted simply by applying the composition onto a member and drying or heating the composition applied to the member. The resultant hydrophilic thin film is transparent and, hence, does not sacrifice the transparency and appearance of a member required to be transparent. Further, the surface of a member with the above composition applied thereto has such a property that water droplets adhered thereon can be immediately removed by vaporization and the surface is less likely to be soiled and, even when a contaminant is adhered thereon, can easily release the contaminant therefrom.

Description

4 6 7 94 經濟、部中央標準局員工消費合作社印製 A7 B7 五、發:明説明( i ) [發明背景] i明領域 本發明係有關於一種組合物,該組合物應用於元件 表面時,可使其高度親水化,並維持其親水性。更特別 的是,本發明係有關於—種組合物,該組合物玎使鏡子 表面’玻璃,鏡片’和其他元件高度親水化,以預防該 物品或元件表面起霧,及形成水滴,或清潔元件表面, 或以蒸發而加速元件表面水滴之除去,而使得物品或元 件表面快速乾燥。 技術背景 當汽車和其他交通工具之擋風玻璃或窗玻璃,建築 物之窗玻璃,眼鏡鏡片,和各種儀表板之蓋玻璃暴露於 寒冷天氣時,常因濕氣凝結而起霧。另外,浴室或洗手 間的鏡子和眼鏡鏡片也常因水蒸汽而變模糊。物件表面 暴露於低於大氣露點之溫度會使得大氣中之濕氣凝結於 物件之表面,形成水滴,而產生霧氣。當凝結的水滴很 小,其直徑約為可見光波長的一半時,水滴會散射光線 ,使得玻璃和鏡子變成不透明,結果亦失去其可見度。 濕氣的再凝結使得凝結的小水滴結合為較大的分離 水滴,使水滴和物件表面界面及水滴和空氣之界面的光 線產生折射現象1而引起物件表面的濁化,模糊,產生 斑點或其他起霧情況。因此,如玻璃等透明物件,透視 影像會被扭曲,降低其透視率’而鏡子則其反射影像會 受到干擾。 本紙張尺度通用中國國家標隼(CMS ) A4规格(210X297公釐} (請先閣讀背面之注意事寫本買) •裝-4 6 7 94 Printed by A7 B7, Consumer Cooperatives of the Central Bureau of Standards, Ministry of Economic Affairs, Ministry of Economic Affairs, and Fifth, issued by: (i) [Background of the Invention] The present invention relates to a composition, which is applied to the surface of a component. , Can make it highly hydrophilic and maintain its hydrophilicity. More specifically, the present invention relates to a composition which highly hydrophilizes the mirror surface 'glass, lenses' and other elements to prevent the surface of the object or element from fogging, forming water droplets, or cleaning The surface of the component, or evaporation, accelerates the removal of water droplets on the surface of the component, so that the object or the surface of the component dries quickly. TECHNICAL BACKGROUND When windshields or window glass of automobiles and other vehicles, window glass of buildings, spectacle lenses, and cover glass of various instrument panels are exposed to cold weather, they often fog due to condensation of moisture. In addition, mirrors and spectacle lenses in bathrooms or washrooms are often blurred by water vapor. Object surface Exposure to a temperature below the dew point of the atmosphere will cause moisture in the atmosphere to condense on the surface of the object, forming water droplets, and generating mist. When the condensed water droplets are small and have a diameter of about half the wavelength of visible light, the water droplets scatter light, making glass and mirrors opaque, and as a result lose their visibility. The re-condensation of moisture combines the condensed small water droplets into larger separated water droplets, causing the light at the interface between the water droplet and the surface of the object and the interface between the water droplet and the air to refract the light. Fog situation. Therefore, for transparent objects such as glass, the perspective image will be distorted, reducing its perspective, and the mirror's reflection image will be disturbed. The paper size is in accordance with the Chinese National Standard (CMS) A4 specification (210X297 mm) (please read the notes on the back first to buy) • Pack-

R -丁 - -$ 4 6 7 94 3 經濟部中央標準局員工消費合作社印製 A7 ______B7五、發明説明(2 ~~;— 另外,當車輛擋風玻璃或窗玻璃,建築物之窗玻璃 ,車輛後視鏡,眼鏡鏡片,和面具或鋼盔護罩暴露於雨 水或被水喷到時,有較大量水滴附著於表面,而使物件 表面產生混濁,模糊,產生斑點或其他起霧情況,結果 又失去了可見度。 不用說,''起霧或濁化"會大大的影響各種工作的安 全性和效率。例如,冷天或雨天時,車輛擋風玻璃或窗 玻璃和車辆後視鏡之起霧或濁化,使得視線不佳,妨害 車輛交通安全。内視鏡,牙科用鏡,和雷射牙科治療儀 器之聚光鏡起霧會妨礙適當的診斷,手術,和治療。儀 表板蓋玻片之起霧會造成數據讀取之困難。 另外,在建築物和塗層方面,環境污染問題也困擾 建桌物’至外建築物的外表材料’及其塗層。天氣良好 時,浮游於空氣中的灰塵和顆粒沈積於建築物的屋頂和 外牆。遇到下雨時,沈積物隨雨水沿建築物外牆流下來 。另外’在多雨的天氣’懸浮的灰塵被雨水攜帶,流至 建築物表面和室外建築物的表面。結果,污物附著於雨 水流經之處。表面乾後,污泥遺留下來成條紋狀。 燃燒產物’如碳黑,城市灰塵,和無機污染物,如 泥土顆粒,建築物外材塗層之土質組成。諸多污染物使 得防污染之測定變得很複雜。參考下面文獻(Yoshinori Kitsutaka > ''Gaiheki Shiage ZairyouNo OsenNo Sokushin Shiken Houhou (Accelerated Testing Method for Contamination of Finish Materials of Outer Wall) ^ (請先聞讀背面之注意事填寫本頁) 装· :1 .線_ 本紙張尺度適用中國國家標準(CNS ) A4規格(210Χ297公嫠) -5 ~ 467943 五、發明説明(3 ) ? Journal of Structural and construction Engineering (Transactions of AIJ), No. 404, October 1989, pp.15-24) ° 到目前為止,使用防水塗料,如聚四氟乙烯(PTFE) ,被認為是用來預防建築物外表等被污染較佳的方法。 然而,近年來的認知,塗層表面盡可能具有親水性,對 含大量疏水性城市灰塵是較有效的(Kobunshi, Vol. 44, May 1995,p.307)。因此,有親水性的接枝聚合物之應 用於建築物塗層的報導(''Japan Chemical Week ",January 30,1995)。根據此報導,該塗層之親水性為,與水之接 觸角為30至40。。 一般泥土無機灰塵,其與水之接觸角為20。至50。,因 此’與水接觸角為30。至40。之接枝聚合物具有親合性,而 很可能附著於其表面。因此,接枝聚合物塗層無法完全 避免無機灰塵的泥化。 [發明摘要說明] 經濟部中央標準局員工消費合作社印製 目前’本發明者發現一種特殊組合物,其中包含金 屬氧化物之光催化顆粒,當它應用於元件表面時,可使 元件表面报容易,而且高度地親水化,而同時保留其高 親水性。本發明即根據此發現而來。 因此’本發明之目的為,提供一種组合物,該組合 物可提供元件表面防霧性。 本發明另一個目標為,提供一種組合物’該組合物 可提供元件表面防霧性,而不犧牲其透明度。 -6 - 經濟部中央標準局貝工消費合作社印製 4 6 7 9 4 3 A7 -—______B7 五、發明説明Y7"T " ~ -- 而本發明另外的—個目標為,提供—種組合物,當 它應用於元件表面時,可加速元件表面水滴之蒸發,而 使元件乾燥。 本發明再-個目標為提供-触合物,該組合物應 用於7C件表®時,可使元件表面不易沾污,即使沾污, 也很谷易被除去。 如本發明之概念,提供一種元件表面親水化之組合 物,其中至少包含 (a) 金屬氧化物之光催化顆粒, (b) 至少一種組成物,其係擇自矽土微細顆粒,一種 可形成矽鲖樹脂薄膜之先驅物和一種可形成矽薄膜之先 驅物所組成之族者,及 (c) 溶劑, 光催化顆粒和石夕土微細顆粒或組合物内先驅物之總 固體含量為0,01至5%重量比。 [圓示簡要說明] 苐1圖為顯不填充本發明組合物之一個較佳喷霧容 器實施例之示意圓; 第2圖為顯示圖1喷霧容器之一個較佳帽蓋實施例之 示意圊; 第3圖為顯示另一個填充本發明組合物之較佳喷霧 谷器實施例之示意圊; 第4圖為顯示另一個填充本發明级合物較佳嗔霧容 器實施例之示意圖;及 本紙張尺度適用中國國家標) Μ规格(2[〇χ29"7公釐) ~ (請先閱讀背面之注意事項r成寫本頁) 裝. 訂 β r -7 - 經濟部中央樣準局員工消費合作社印製 467943 A7 五、發明説明(5 ) 第5圖(a)和(b)為顯示構成填充本發明組合物喷霧 各器之氣球的截面示意圖; 第6圖為顯示實例A4製備之親水性表面的防霧性, 以紫外光照射時間為函數之變化圖;及 第7圖為顯示實例B1製備之親水性表面的防霧性, 以紫外光照射時間為函數之變化圖。 [發明詳細說明] ΜΛ 此處使用之防霧"係泛指預防表面因水滴凝結而起 霧或混濁,所引起之光學困擾。 親水性砉面 本發明組合物,以下述方法應用至元件表面後,可 使元件表面親水化。較佳的,親水化之表面可被水浸濕 ’而使該表面和水之接觸角不大於10。,更佳的是不超過 5。。 另外,本發明組合物的優點是可使元件表面高度親 水化,而同時保留其透明度。可使需要透明之元件具有 親水性,尤其是防霧性,而不必犧牲透明度和外觀是本 發明極大的優點。另外的大優點是,只要將本發明組合 物應用至一個元件表面’乾燥或加熱,就很容易提供該 元件親水性。當然,組合物應用至元件表面時,依操作 方式不同’會有薄膜厚度不同或不均勻情況發生。然而 ’如本發明組合物,調控组合物之用量,以得到下面描 述之薄膜厚度,並選擇應狀方法,以㈣均勻的薄^ 本紙浪尺度適用中國國家揉準(CNS ) A4規格(2丨OX297公釐---- -8 - .I-J'i —-It ^^^1 i^n. HI n • - U3 (請先閱讀背面之注意事\^"-寫本頁)R-丁--$ 4 6 7 94 3 Printed A7 ______B7 printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs V. Invention Description (2 ~~; In addition, when the vehicle windshield or window glass, building window glass, Vehicle rearview mirrors, spectacle lenses, and masks or helmet shields are exposed to rain or sprayed with water, and a large amount of water droplets adhere to the surface, which makes the surface of the object cloudy, fuzzy, and spots or other fogging conditions. Visibility is lost again. Needless to say, "fogging or clouding" will greatly affect the safety and efficiency of various tasks. For example, in cold or rainy days, the vehicle windshield or window glass and the vehicle rearview mirror Fogging or clouding makes poor visibility and obstructs vehicle traffic safety. Fogging of endoscopes, dental mirrors, and condensers of laser dental instruments can prevent proper diagnosis, surgery, and treatment. Cover of instrument panel The fog of the film will make it difficult to read the data. In addition, in terms of buildings and coatings, environmental pollution problems also plague the building's 'to the exterior materials of the building' and its coating. When the weather is good, the floating Dust and particles swimming in the air are deposited on the roof and external walls of the building. When it rains, the sediment flows down along the external wall of the building with rain. In addition, the suspended dust is carried by rain in 'rainy weather'. It flows to the surface of buildings and the surface of outdoor buildings. As a result, dirt adheres to where rainwater flows. After the surface is dry, sludge is left in stripes. Combustion products such as carbon black, urban dust, and inorganic pollutants , Such as soil particles, the soil composition of the building exterior coating. Many pollutants make the measurement of pollution prevention very complicated. Refer to the following literature (Yoshinori Kitsutaka > '' Gaiheki Shiage ZairyouNo OsenNo Sokushin Shiken Houhou (Accelerated Testing Method for Contamination of Finish Materials of Outer Wall) ^ (Please read and read the notes on the back to complete this page) Assembly:: 1. Thread_ This paper size is applicable to China National Standard (CNS) A4 specification (210 × 297 cm) -5 ~ 467943 5 2. Description of the invention (3)? Journal of Structural and construction Engineering (Transactions of AIJ), No. 404, October 1989, pp. 15-24 ) ° So far, the use of waterproof coatings, such as polytetrafluoroethylene (PTFE), is considered to be a better method to prevent contamination of the exterior of buildings. However, in recent years, it has been recognized that the coating surface is as hydrophilic as possible. It is more effective for large amounts of hydrophobic urban dust (Kobunshi, Vol. 44, May 1995, p. 307). Therefore, there have been reports of applications of hydrophilic graft polymers in building coatings (`` Japan Chemical Week ", January 30, 1995). According to this report, the coating has a hydrophilicity of 30 to 40 on the contact angle with water. . Generally, the soil inorganic dust has a contact angle of 20 with water. To 50. Therefore, the contact angle with water is 30. To 40. The graft polymer has an affinity and is likely to adhere to its surface. Therefore, the grafted polymer coating cannot completely prevent the sludge of inorganic dust. [Abstract Description of the Invention] Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs, the present inventor has found a special composition containing photo-catalytic particles of metal oxides. When it is applied to the surface of a component, the surface of the component can be easily reported. And is highly hydrophilic while retaining its high hydrophilicity. The present invention is based on this finding. It is therefore an object of the present invention to provide a composition which can provide anti-fogging properties to the surface of a device. Another object of the present invention is to provide a composition 'which can provide anti-fogging property to the surface of a component without sacrificing its transparency. -6-Printed by the Shellfish Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs 4 6 7 9 4 3 A7 ---______ B7 V. Description of the Invention Y7 " T " ~-And the other object of the present invention is to provide-a combination When it is applied to the surface of a component, it can accelerate the evaporation of water droplets on the surface of the component and dry the component. Another object of the present invention is to provide a contact compound. When the composition is applied to a 7C watch, the surface of the element is not easily stained, and even if it is stained, it is easily removed. According to the concept of the present invention, a component surface hydrophilizing composition is provided, which comprises at least (a) photocatalytic particles of metal oxides, and (b) at least one composition selected from fine silica particles, and one of which can form The family consisting of a precursor of a silicon thin film and a precursor capable of forming a silicon thin film, and (c) the total solid content of the solvent, the photocatalytic particles and the fine particles of the stone or the precursor in the composition is 0, 01 to 5% by weight. [Circumscription Brief Description] 苐 1 is a schematic circle of a preferred spray container embodiment showing that the composition of the present invention is not filled; FIG. 2 is a schematic view showing a preferred cap embodiment of the spray container of FIG. 1圊; Figure 3 is a schematic view showing another preferred embodiment of the spray mister filled with the composition of the present invention; Figure 4 is a schematic view showing another embodiment of the preferred spray mist container filled with the composition of the present invention; And this paper size applies Chinese national standard) M size (2 [〇χ29 " 7mm) ~ (Please read the precautions on the back to write this page). Order β r -7-Central Bureau of Standards, Ministry of Economic Affairs Printed by the employee consumer cooperative 467943 A7 V. Description of the invention (5) Figures 5 (a) and (b) are schematic cross-sectional views showing the balloons constituting the sprayer filled with the composition of the present invention; Figure 6 is prepared to show Example A4 The antifogging property of the hydrophilic surface as a function of ultraviolet light irradiation time; and FIG. 7 is a graph showing the antifogging property of the hydrophilic surface prepared by Example B1 as a function of ultraviolet light irradiation time. [Detailed description of the invention] ΜΛ The anti-fogging used herein refers to the prevention of optical distress caused by fogging or turbidity caused by condensation of water droplets on the surface. Hydrophilic noodles The composition of the present invention can be made hydrophilic on the surface of the device by the following method. Preferably, the hydrophilized surface may be wetted with water so that the contact angle between the surface and water is not greater than 10. , More preferably no more than 5. . In addition, the composition of the present invention has the advantage that the surface of the element can be highly hydrophilized while retaining its transparency. It is a great advantage of the present invention that the element that needs to be transparent can be made hydrophilic, especially anti-fog, without sacrificing transparency and appearance. Another great advantage is that as long as the composition of the present invention is applied to a surface of an element 'to dry or heat, it is easy to provide the element with hydrophilicity. Of course, when the composition is applied to the surface of the device, different or uneven film thicknesses may occur depending on the operation method. However, as for the composition of the present invention, the amount of the composition is adjusted to obtain the thickness of the film described below, and the method of application should be selected to make the film uniform and thin. ^ This paper applies the Chinese National Standard (CNS) A4 standard (2 丨OX297mm ---- -8-.I-J'i —-It ^^^ 1 i ^ n. HI n •-U3 (Please read the notes on the back first \ ^ " -Write this page)

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-線----— I 467943 A7 _____ B7__ 五、發明説明(6 ) ,可以很容易地得到上述良好的親水性的表面。 經濟部中央樣準局員工消費合作社印製 為了使塗敷组合物的元件親水化,該表面以光線照 射。親水化現象被認為是經由下面的反應機制進行的。 然而’此反應機制只是假說性的,而不是限制本發明的 fe圍。當給予光線’其能量尚於光催化劑價電子帶上限 和傳導電子帶下限間之能差’使得價電子帶之電子發生 光激作用,而產生傳導電子和空洞。其中之任何一個或 一者同時用於提供光催化劑表面的極性(可能是拉電子性 質)。如此可使得比大氣平衡之水量更多的水分,以化學 吸附於表面。然後,增加了氫鍵誘引之表面自由能’產 生物理吸附,使得因表面自由能的增加,而增加水分子 附著於表面之數量。一般而言,當一個物質的表面自由 能接近另一種物質的表面自由能時,這些物質报可能互 相黏著。因此,水分子以物理性吸附於表面,而具有良 好的水潤濕性,也就是說該表面親水化了。另外,本發 明組合物提供的表面親水化的程度並不決定於該組合物 薄膜之厚度。已經知道一個光催化劑具有氧化性 性,而含光催化劑之薄膜因為這活性而具有抗污染,抗 菌,和除臭的效果。本發明者已確認此氧化性分解的二 性取決於含光催化劑薄膜的厚度。另外,本發明者已確 認,本發明組合物薄膜的厚度誘引之親水化,足以使得 氧化性分解活性非常低或甚至沒有。再者,本發明者^ 確認,本發明組合物提供之薄膜,其厚度可以小至不縈 響透明元件之透明度,氡化性分解活性是很有限的,或7 本紙張適财國國家操準(CNS ) A4規格(21()χ29»麓) 467943 Α7 ' _ Β7 五、發明説明(.7 ) 者在有些情況下,根本沒有。 當表面親水化之後,即使放置於黑暗處,該親水性 也可以維持星期。 為了以光催化劑之光激作用使表面高度親水化,激 發光之照射強度較佳的是不少於〇 〇〇1 mff/cm2,更佳的是 不少於0·01 mff/cm2,最佳的是不少於01 raW/cm2。 當光催化氧化物為銳鈦礦氧化鈦,金紅石氧化鈦, 氧化鋅,或鈦酸锶時,日光,室内燈,螢光燈,水銀燈 ,白熱燈,氙氣燈,高壓鈉燈,金屬鹵素燈,BLB燈等可 適用為光催化劑光激作用之光源。另外,當光催化氧化 物為氧化錫時,滅菌燈,BLB燈等可適用為光源。 使用本發明組合物於元件表面所形成之表層厚度較 佳的是不超過0,4μιη。當它不超過〇.〇4μπι時,可避免不規 則反射引起的混濁現象,所以表層實質上是透明的。為 了有效避免光線干擾產生的表層顏色的產生,其表面厚 度更佳的是不超過〇. 2μπ}。表層厚度愈小,表層透明度愈 好’同時’抗損性愈好, 經濟部中央標準局員工消費合作社印製 如本發明之一個較佳實施例,以此法得到之表層,其 光催化劑含量較佳的是約1><1〇-7至1><1〇-;^/(^2,更佳的 疋約5X10 7至5xi〇-4g/cm2,最佳的是约至 4g/cm2 。 甚至當空氣中的濕氣或水蒸汽凝結於本發明組合物 咼度親水化的表面時,凝結的水根可能形成均勻的水薄 膜,而不是分離的水滴。因此,在元件表面不會產生光 ΐ紙張以適财關家榡^JCNS)續格(210χ-^^----- -ίο - 6 7 943 Α7 __ Β7 五、發明説明(8 ) 線散射霧。同樣的’車輛窗玻璃,後視鏡,交通工具之 擋風玻璃,眼鏡鏡片,和鋼盔護罩暴露於雨水或喷到水 時,不會形成分離的水滴’而影響視線,因為附著於這 些物件表面的水滴’會迅速地分散成均勻的水薄膜。如 此確保良好的視線和可見度,因而確保交通車輛安全, 而增進各種工作和活動的效率。 另外,各種形式的污染物’如城市灰塵,汽車廢氣 内的破黑等燃燒產物,脂肪和油,和填缝料釋出之成分 專疏水性污染物’和無機泥材污染物,也較不容易黏著 於本發明組合物南度親水化的表面,甚至在黏著之後也 可以很容易地被雨水或洗蘇水沖洗掉。 另外,本發明組合物高度親水化的表面使得黏著之 水滴分散於表面,其以蒸發加速水滴之除去。 另外’本發明組合物高度親水化的表面具有抗靜電 性效果(避免灰塵沈積的效果),熱絕緣效果,預防水下 氣泡積存的效果,增進熱交換效率的效果,和增加生物 相容性的效果。 經濟部中央襟準局員工消費合作社印製 當本發明組合物被用於防霧效果時,組合物應用之 元件通常是清澈的。元件的材料並不特別受限制,其實 例包括玻璃和塑膠。組合物可應用的元件之特殊實例包 括鏡子,如車輛後視鏡,浴室鏡子,洗手間鏡子,牙科 用口腔鏡,道路反射鏡;鏡片,如眼鏡鏡片,光學透鏡 ,fe光鏡,半導體透鏡,影印機透鏡,車輛後視照相鏡 片;稜鏡;建築物或觀測台窗玻璃;車輛窗破璃,如汽 本紙張财關家鮮{ CNS〉Α4· ( 210X297公釐)-— '11- 467943 A7 B7 五 經濟部中央標準局員工消費合作衽印 發明説明( 雀路車輛,飛機,水運工具,潛水艇,雪車,雪地 人通工具,空中纜車吊籃,休閒花園平底船和太空船; 車輛撞風麵,如汽車,摩托車,麟車輛,飛機,水 運工具,潛水艇,雪地交通工具,空中纜車吊籃’休閒 花園平底船和太空船;護目鏡,運動護目鏡,面具護罩 ’運動面具護罩,鋼纽罩,冷束食品展示盒玻璃,如 中國麵&之保溫食品展示盒玻璃;測量儀器蓋罩,車輛 後視照相鏡>1蓋罩’雷射牙科治療儀器聚光鏡蓋罩,雷 射光偵測探頭蓋罩’如車輛裂縫偵測探測器蓋罩,紅外 .光探測H蓋罩U目㈣光鏡;和其他驗上述物件表 面的薄膜’薄片,封朦等等。 另外田本發明組合物被用為表面清潔效果時,元 件的材料並不特別受限制,其實例包括金屬,陶瓷,玻 璃,塑膠’木材’石材,水泥,混凝土,纖維,羊毛織 品,和上述材料之組合,及上述材料製成之薄片。組合 物可應用的元件之特殊實例包括建築物材料,建築物外 觀’建築物内部’窗框,窗玻璃,結構元件,車輛外觀 和塗層,機械和物件外觀,防塵罩和塗層,交通信號, 各種顯示裝置,廣告塔或海報攔,道路噪音障壁,鐵路 噪音障壁’橋樑’護欄外觀和塗層,隨勒面和塗層, 絕緣體’太陽能電池蓋罩,太陽能熱水器太陽能收集器 蓋軍,乙稀Μ溫室’車柄,家用品,馬桶,浴缸,洗 盆之照光蓋罩’照光設備,照光蓋罩,廚房用品,餐桌 用品,洗碗機’烘碗機,水槽,烹飪區,油煙機,排風 本紙張錢適I中關家標準(CNS ) Α4規格(2〗G>^97公釐 -12 6 7 94 A7 B7 經濟部中央榇準局員工消費合作社印製 五 '發明説明(I0) 扇,和其他用於上述物件表面的薄膜,薄片,封膠等等 0 另外’當本發明組合物仙為以蒸發加速除去水滴 之效果時,元件的材料並不特別受限制,其實例包括金 屬,陶曼’玻璃,塑膠,木材’石材,水泥,混凝土, 纖維,羊毛織品,和上述材料之組合,及上述材料製成 2薄片。組合物可應用的元件之特殊實例包括汽車體, 窗子,鋪路材料,和其他用於上述物件表面的薄膜,薄 片,封膠等等。 另外,當本發明组合物被用為抗靜電性之效果時, 元件的材料並不特別受限制,其實.例包括金屬,陶究., 玻璃,塑膠,木材,石材,水泥,混凝土,纖維,羊毛 織品,和上述材料之組合,及上述材料製成之薄片。組 合物可應用的元件之特殊實例包括陰極光管;磁性載聲 體;光學載聲體,·光磁載聲體;錄音帶;錄影帶;類比 唱片,家庭電器周品收藏盒,零件,外殼和塗層;辦公 室自動化設備之收藏盒,零件,外殼和塗層;建築物材 料;建築物外殼,·窗框;窗玻璃;結構元件;車輛外殼 和塗層;機械和物件外殼;防塵罩和塗層;和其他用於 上述物件表面的薄膜,薄片,封勝等等。 表面親水仆.細各物 如本發明之組合物,基本上包含 Ca)金屬氧化物光催化顆粒, (b)至少一種組成物,其係擇自矽土微細顆粒,一種-Line ----— I 467943 A7 _____ B7__ 5. Description of the invention (6), the above-mentioned good hydrophilic surface can be easily obtained. Printed by the Consumer Cooperative of the Central Bureau of Procurement, Ministry of Economic Affairs. To hydrophilize the components of the coating composition, the surface is illuminated with light. The phenomenon of hydrophilization is considered to proceed through the following reaction mechanism. However, this reaction mechanism is only hypothetical and does not limit the fe range of the present invention. When light is given, its energy is still the energy difference between the upper limit of the valence band of the photocatalyst and the lower limit of the conduction electron band. Either or both of them are used to provide the polarity of the photocatalyst surface (probably electron-drawing properties). This allows more water to be chemically adsorbed on the surface than the atmospheric equilibrium water. Then, the surface free energy 'induced by hydrogen bonding is increased to generate physical adsorption, so that the number of water molecules attached to the surface is increased due to the increase of the surface free energy. In general, when the surface free energy of one substance is close to the surface free energy of another substance, these substances may adhere to each other. Therefore, water molecules are physically adsorbed on the surface and have good water wettability, that is, the surface is hydrophilized. In addition, the degree of hydrophilization of the surface provided by the composition of the present invention does not depend on the thickness of the film of the composition. It is known that a photocatalyst is oxidizing, and a film containing a photocatalyst has antifouling, antibacterial, and deodorizing effects due to this activity. The present inventors have confirmed that the amphipathic nature of this oxidative decomposition depends on the thickness of the photocatalyst-containing film. In addition, the present inventors have confirmed that the thickness of the film of the composition of the present invention induced hydrophilization is sufficient to make the oxidative decomposition activity very low or even absent. Furthermore, the inventor ^ confirmed that the thickness of the film provided by the composition of the present invention can be as small as not to affect the transparency of the transparent element, and the chemical decomposition activity is very limited, or 7 papers are suitable for the countries of the financial country (CNS) A4 specification (21 () χ29 ») 467943 Α7 '_ Β7 V. Description of invention (.7) In some cases, there is no such thing at all. When the surface is hydrophilized, the hydrophilicity can be maintained for a week even when placed in a dark place. In order to make the surface highly hydrophilized by the photocatalytic effect of the photocatalyst, the irradiation intensity of the excitation light is preferably not less than 0.001 mff / cm2, and more preferably not less than 0.01 mff / cm2, and the best It is not less than 01 raW / cm2. When the photocatalytic oxide is anatase titanium oxide, rutile titanium oxide, zinc oxide, or strontium titanate, daylight, indoor lamp, fluorescent lamp, mercury lamp, incandescent lamp, xenon lamp, high-pressure sodium lamp, metal halide lamp, BLB lamps and the like can be used as light sources for photocatalytic photoexcitation. In addition, when the photocatalytic oxide is tin oxide, a sterilization lamp, a BLB lamp, etc. can be suitably used as the light source. The thickness of the surface layer formed on the surface of the element by using the composition of the present invention is preferably not more than 0.4 μm. When it does not exceed 0.04 μm, turbidity caused by irregular reflection can be avoided, so the surface layer is substantially transparent. In order to effectively avoid the occurrence of surface color caused by light interference, its surface thickness is more preferably not more than 0.2 μπ}. The smaller the thickness of the surface layer, the better the transparency of the surface layer, and the better the resistance to damage. The Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs printed a preferred embodiment of the present invention. It is preferably about 1 > < 1〇-7 to 1 > <1〇-; ^ / (^ 2, more preferably about 5X10 7 to 5xi-4g / cm2, and most preferably about 4g / cm2. Even when moisture or water vapor in the air condenses on the highly hydrophilized surface of the composition of the present invention, the condensed water roots may form a uniform water film instead of separated water droplets. Therefore, the component surface will not Generate light-emitting paper to meet the financial needs of the family ^ JCNS) Continuation (210χ-^^ ----- -ίο-6 7 943 Α7 __ Β7 V. Description of the invention (8) Linear scattering fog. The same 'vehicle window When glass, rearview mirrors, windshields, eyeglass lenses, and helmet shields of vehicles are exposed to rain or sprayed with water, they will not form separated water droplets, which will affect vision, because water droplets attached to the surface of these objects will Disperses quickly into a uniform water film. This ensures good line of sight and visibility, so To ensure the safety of traffic vehicles, and to improve the efficiency of various tasks and activities. In addition, various forms of pollutants' such as urban dust, combustion products such as car exhaust black, fats and oils, and the components released from joint compounds are specifically hydrophobic. Sexual pollutants' and inorganic mud pollutants are also less likely to adhere to the south-hydrophilized surface of the composition of the present invention, and can even be easily washed away by rainwater or washing water even after adhesion. In addition, the present invention The highly hydrophilized surface of the composition disperses the adhered water droplets on the surface, which accelerates the removal of the water droplets by evaporation. In addition, the highly hydrophilized surface of the composition of the present invention has antistatic effect (effect of preventing dust deposition) and thermal insulation effect. , The effect of preventing the accumulation of underwater bubbles, the effect of improving heat exchange efficiency, and the effect of increasing biocompatibility. Printed by the Consumer Cooperative of the Central Government Bureau of the Ministry of Economic Affairs. When the composition of the present invention is used for anti-fog effect, the combination The components used in physical applications are usually clear. The materials of the components are not particularly limited, and examples thereof include glass and plastic. Combination Specific examples of applicable elements include mirrors such as vehicle mirrors, bathroom mirrors, toilet mirrors, dental mirrors, road mirrors; lenses such as spectacle lenses, optical lenses, fe mirrors, semiconductor lenses, photocopiers Lens, vehicle rear view photographic lens; 稜鏡; building or observation platform window glass; vehicle window broken glass, such as steamed paper, paper property, and fresh food {CNS> Α4 · (210X297 mm) -— '11-467943 A7 B7 The 5th Ministry of Economic Affairs, Central Bureau of Standards, consumer cooperation, printed the invention description (queu vehicles, aircraft, watercraft, submarines, snowmobiles, snowmobiles, aerial cable car baskets, leisure garden punts and spaceships; vehicles collided Wind surface, such as cars, motorcycles, lin vehicles, airplanes, watercraft, submarines, snowmobiles, gondola gondola 'leisure garden punts and space ships; goggles, sports goggles, mask shields' sports Mask cover, steel button cover, cold beam food display box glass, such as Chinese noodles & insulation food display box glass; measuring instrument cover, vehicle rearview camera mirror> 1 cover Laser dental treatment instrument condenser cover, laser light detection probe cover 'such as vehicle crack detection detector cover, infrared. Light detection H cover U eye lens; and other films on the surface of the object' thin sheet , Feng Hao and so on. In addition, when the composition of the present invention is used as a surface cleaning effect, the material of the element is not particularly limited. Examples thereof include metal, ceramic, glass, plastic 'wood' stone, cement, concrete, fiber, woolen fabric, and the above materials. Combination, and flakes made of the above materials. Specific examples of components to which the composition can be applied include building materials, building exterior 'building interior' window frames, window glass, structural elements, vehicle appearance and coatings, machinery and object appearances, dust covers and coatings, traffic signals , Various display devices, advertising towers or posters, road noise barriers, railway noise barriers' bridge 'guardrail appearance and coatings, graffiti and coatings, insulators' solar cell covers, solar water heater solar collector cover army, B Thin M greenhouse 'handle, houseware, toilet, bathtub, basin light cover' light equipment, light cover, kitchenware, tableware, dishwasher 'dishwasher, sink, cooking area, cooker hood, Exhaust this paper money suitable I Zhongguanjia standard (CNS) Α4 specifications (2) G > ^ 97 mm-12 6 7 94 A7 B7 Printed on the five 'Invention Note (I0) by the Consumers' Cooperative of the Central Bureau of Quasi-Bureau of the Ministry of Economic Affairs Fans, and other films, sheets, sealants, etc. used on the surface of the above-mentioned objects. In addition, when the composition of the present invention has the effect of accelerating the removal of water droplets by evaporation, the material of the element is not special. Restricted, examples of which include metal, Taumann 'glass, plastic, wood' stone, cement, concrete, fiber, woolen fabric, and combinations of the above materials, and the above materials are made into 2 sheets. Special components of the composition can be applied Examples include automobile bodies, windows, paving materials, and other films, sheets, sealants, etc. used on the surface of the above-mentioned objects. In addition, when the composition of the present invention is used for the effect of antistatic property, the material of the element is not particularly Restricted, in fact, examples include metals, ceramics, glass, plastic, wood, stone, cement, concrete, fiber, woolen fabrics, combinations of the above materials, and flakes made of the above materials. Components that can be applied to the composition Specific examples include cathode light tubes; magnetic sound carriers; optical sound carriers; optical magnetic sound carriers; audio tapes; video tapes; analogue records, household appliances, storage boxes, parts, housings and coatings; office automation equipment Collection boxes, parts, shells and coatings; building materials; building shells, window frames; window glass; structural elements; exterior of vehicles And coatings; machinery and object housings; dust covers and coatings; and other films, sheets, seals, etc. used on the surface of the above objects. Surfaces are hydrophilic. Fine objects such as the composition of the present invention basically contain Ca ) Metal oxide photocatalytic particles, (b) at least one composition selected from silica fine particles, a

Jlir—II裝------訂-----線____ (請先閲讀背面之注意事f-'人填寫本頁) 」 i • - - 1 1 ^紙張;^逍财國國巧準(CNS) A4規格(2!gx297公董) — i— I 1 1 - -1 4 6 7 943 經濟部中央標準局員工消費合作社印製 五、發明説明(η ) ; 可形成㈣樹㈣臈之先驅物和—種可形㈣薄膜之先 驅物所組成之族者,及 (c)Ml另外’如有必要,本發明組合物可包含另 外的組成份。 先催化顆粒 包含於本發明組合物之光催化齡,基本上包含— 種金屬氧化物1別的’在本發日种,所謂''光催化劑〃 意指一種犲料1當給予光線(激發光),其能量高(短 波長)於光敍_電子帶上限和料電子帶下限間之 能差,使得價電子帶電子發生光激作用,而產生傳導電 子和空洞。可用於此處之光催化氧化物包括,例如,銳 欽擴f化鈦,金紅石氧滅,氧化鋅,氧㈣,乳化鐵 ,二氧化二叙,三氧化鎢,和鈦酸錯。 光催化顆粒之平均結晶直徑較佳的是不超過1〇〇nm。 結晶物平均直徑上限較佳的是約2〇nm,更佳的是約1〇nm 。平均結晶直徑下限較佳的是約i nm,更佳的是約3nm。 光催化顆粒在上述平均結晶直徑範圍内者可使表面親水 化,而避免層塗之表面因顆粒弓丨起可見光散射,而失去 其透明度。 光催化顆粒之平均結晶直徑之測定,是以粉末χ—光 繞射儀’取得顆粒在最大強度2Θ=25. 3。之峰寬積分,依照the Scherrer 's equation計算而得。 和矽酮榭脂簿膜和矽薄膜先駆物 本發明組合物包含矽土微細顆粒。矽土可有效地使 本紙張尺&適用中國國家標準(CNS ) A4規格(21〇><297公釐) I - I - « I I. —II · Μ--7.^----- — 裝--- -f (請先閱讀背面之注意事寫本頁) _ -訂.1 線_ 14 -Jlir—II Pack ------ Order ----- Line ____ (Please read the note on the back f-'Person to fill out this page)》 i •--1 1 ^ 纸; ^ 逍 财 国Manual (CNS) A4 specification (2! Gx297 public director) — i— I 1 1--1 4 6 7 943 Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 5. Description of invention (η); can form a linden tree The precursors of tritium and a precursor of a tangible tritium thin film, and (c) M1. In addition, if necessary, the composition of the present invention may contain additional components. The first catalytic particles are included in the photocatalytic age of the composition of the present invention, and basically include-a kind of metal oxide 1 and the other "in the present day, the so-called" photocatalyst "means a kind of material 1 when given light (excitation light) ), Its energy is high (short wavelength) between the upper limit of the optical electron band and the lower limit of the material electron band, which makes the valence electrons undergo photoexcitation, which generates conductive electrons and voids. Photocatalytic oxides that can be used herein include, for example, uranium titanium oxide, rutile oxanthine, zinc oxide, osmium, emulsified iron, dioxane, tungsten trioxide, and titanate. The average crystal diameter of the photocatalytic particles is preferably not more than 100 nm. The upper limit of the average crystal diameter is preferably about 20 nm, and more preferably about 10 nm. The lower limit of the average crystal diameter is preferably about 1 nm, and more preferably about 3 nm. Those with photocatalytic particles within the above-mentioned average crystal diameter range can hydrophilize the surface, and prevent the surface of the layer coating from scattering visible light due to the particle bow, thereby losing its transparency. The determination of the average crystal diameter of the photocatalytic particles was carried out with a powder χ-light diffractometer 'to obtain the particles at a maximum intensity of 2Θ = 25.3. The peak width integral is calculated according to the Scherrer's equation. Precursor with silicone film and silicon film The composition of the present invention contains fine particles of silica. Silica can effectively make this paper rule & apply Chinese National Standard (CNS) A4 specification (21〇 < 297 mm) I-I-«I I. —II · Μ--7. ^- --- — Install --- -f (Please read the notes on the back to write this page) _ -Order. 1 Thread _ 14-

光催化顆粒固定於元件表面。如本發明一個較佳的實施 例,矽土微細顆粒平均顆粒直徑範圍為丨至丨⑼nm,較佳 的是5至50nm,最佳的是8至20nm。其直徑可以用動能雷 4 67 943 射散射方法測定。 可用於本發明組合物可形成矽薄膜之先驅物的一個 較佳實例為,具有下面平均組合物化學式之矽酸鹽:The photocatalytic particles are fixed on the surface of the element. According to a preferred embodiment of the present invention, the average particle diameter of the fine silica particles ranges from 丨 to 至 nm, preferably from 5 to 50 nm, and most preferably from 8 to 20 nm. Its diameter can be measured by the kinetic energy lightning 4 67 943 radiation scattering method. A preferred example of a precursor that can be used in the composition of the present invention to form a silicon film is a silicate having the following average composition chemical formula:

SiXC!0(4_Ci)/2 其中,X代表烷氧基或齒素原子,而q為滿足〇<q<4之 數目。 另一個可用於本發明組合物之可形成聚矽塗層先驅 物實例為,四官能基,可水解的矽烷衍生物,以下列化 學通式代表:SiXC! 0 (4_Ci) / 2 wherein X represents an alkoxy group or a halogen atom, and q is a number satisfying 0 < q < 4. Another example of a polysilicon coating precursor that can be used in the composition of the present invention is a tetrafunctional, hydrolyzable silane derivative, represented by the following chemical formula:

SiX4 其中X為烷氧基或鹵原子。 較佳的四官能基特殊實例如,可水解之矽炫衍生物 包括四甲氧基矽烷,四乙氧基矽烷,四丙氧基矽烷,四 丁氧基矽烷,二乙氧基二甲氧基矽烷,四氣矽烷,四溴 矽烷,矽醇,和二甲氧基二乙氧基矽烷。 較佳的矽酸鹽特殊實例包括,該四官能基,可水解 之矽烷衍生物部份之水解產物和脫氫聚縮合產物。 可用於本發明組合物之可形成矽薄膜聚矽塗層先驅 物之一較佳實例,為以下列平均組合物化學式代表之矽 氧烷:SiX4 where X is an alkoxy group or a halogen atom. Specific examples of preferred tetrafunctional groups include, for example, hydrolyzable siloxane derivatives including tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetrabutoxysilane, diethoxydimethoxy Silane, tetragas silane, tetrabromosilane, silanol, and dimethoxydiethoxysilane. Specific examples of preferred silicates include the tetrafunctional group, a hydrolysate of a hydrolyzable silane derivative moiety, and a dehydropolycondensation product. A preferred example of a precursor for forming a silicon thin film polysilicon coating that can be used in the composition of the present invention is a siloxane represented by the following average composition chemical formula:

KpSiXq〇(4_p )/2 本纸張尺度適用中國國家標準(CNS ) Α4· 297公釐) (請先聞讀背面之注意事填寫本頁) ,-----裝------訂------線! 經濟部中央標準局員工消費合作社印製 _ 15 - 467943 經濟部中央標準局員工消費合作社印製 A 7 _B7__五、發明説明(13 ) 其中,R代表擇自包含氫原子和一個或更多個有機族 群之一者; X代表烧氧基或i素原子;及 p為滿足0<p<2之數目,而q為滿足0<q<4之數目。 可用於本發明組合物可形成矽薄膜之聚矽塗層先驅 物之一較佳實例,為以下列化學通式代表之可水解矽烷 4 衍生物:RPSiVP 其中,R為如上述定義; X代表烷氧基或iS素原子;及 p為1或2. 在這種情況下,R代表的有機官能機較佳的是烷基( 更佳的是具有1至18碳原子,無取代之烷基,最佳的是具 有3至18碳原子烷基)或芳香基(較佳的是苯基)。. 可水解矽烷衍生物較佳的特殊實例包括,甲基三曱 氧基矽烷,曱基三乙氧基矽烷,甲基三丙氧基矽烷,曱 基三丁氧基矽烷,乙基三甲氧基矽烷,乙基三乙氧基矽 烷,乙基三丙氧基矽烷,乙基三丁氧基矽烷,苯基三甲 氧基矽烷,苯基三乙氧基矽烷,苯基三'丙氧基矽烷,苯 基三丁氧基矽烷,二曱基二曱氧基矽烷,二甲基二乙氧 基矽烷,二甲基二丙氧基矽烷,二甲基二丁氧基矽烷, 二乙基二f乳基梦烧’二乙基二乙氧基石夕烧’二乙基二 丙氧基矽烷,二乙基二丁氧基矽烷,苯基甲基二甲氧基 矽烷,苯基甲基二乙氧基矽烷,苯基甲基二丙氧基矽烷 (請先閱讀背面之注意事^^寫本頁) 裝 訂 線 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 467943 經濟部中央標準局貝工消費合作社印製 A 7 __B7_五、發明説明(14 ) ,苯基曱基二丁氧基矽烷,正-丙基三曱氧基矽烷,正-丙基三乙氧基矽烷,正-丙基三丙氧基矽烷,正-丙基三 丁氧基矽烷,γ-糖氧基丙基三曱氧基矽烷,和γ-丙烯氧基 丙基三曱氧基矽烷' 矽氧烷可由可水解的矽烷衍生物之部份水解而後脫 氫之聚縮合反應而製備,或由可水解的石夕烧衍生物部分 水解產物與四曱氧基矽烷,四乙氧基矽烷’四丙氧基矽 烷,四丁氧基矽烷,二乙氧基二甲氧基矽烷等化合物之 部分水解產物脫氫聚縮合而製備。 依照下面方法,由上述先驅物部分水解或脫氫聚縮 合而製備之矽酮樹脂,以下列平均組合物化學式代表: RpSiO(4-p)/2 ⑴ 其中,R為如上述定義; X為烷氧基或!S素原子;及 p為滿足0<ρ<2之數目。 本發明組合物先驅物之含量可以適當地決定。例如 ,以光催化顆粒一份重量比來說,先驅物,換算為矽土 含量,其含量之上限較佳的是10份重量比,更佳的是5份 重量比,最佳的是1份重量比,而先驅物含量下限較佳的 是0.05份重量比,更佳的是0.1份重量比,而最佳的是0.2 份重量比。 溶劑 本發明組合物之溶劑沒有限制,只要它可安定地分 散光催化顆粒和先驅物,而最終提供一個親水化的表面 (諳先閱讀背面之注意事\^^寫本頁) 裝· I ‘訂- 線_ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -17 - 467943 經濟部中央標準局員工消費合作社印裝 A7 --— _B7__ 五、發明説明(15 ) 。可用於此處的溶劑實例包括水,和有機溶劑,及水和 有機溶劑的混合溶劑。水,醇類,或水和醇類組成的混 合溶劑是特別好的。 . 光催化顆粒重量和矽土微細顆粒重量之總和,或先 驅物重量’換算為矽土,(此總含量稱為'、固體含量")為 超過0.01至不超過5%本發明組合物重量比6固體含量可 用下面方法測定。組合物(重量:A)於400至500°C加熱3小 時以除去液體組成,測量殘餘物之重量(重量:B),再以 下面方程式計算固體含量: 固體含量(%)=(B/A) X100 當固體含量超過5%重量比,組合物表面會因起霧或有干_ 擾邊緣而有不良外觀。固體含量上限較佳的是不超過以 重量比。當固體含量少於0.01%重量比,可能無法有效地 得到親水性表面。固體含量之下限較佳的是0.05%重量比 最t的疋0.1%重置比。在本發明組合物裡面,溶劑的 用量是使光催化顆粒和先驅物之固體含量在上述範圍内 〇 如本發明一個較佳的實施例,使用之醇類,其分子 量為60至300,較佳為60至1〇〇,而且在室溫時是液體較 好的。 此處所用之較佳的醇類之實例包括曱醇,乙醇,正— 丙醇’異丙醇,三級丁醇’異丁醇,正丁醇,2_甲基丙 醇,戊醇,乙二醇’單丙酮醇,二丙酮醇,乙二醇單甲 基麵,4-輕基-4-甲基-2,戊嗣,二丙二酵,丙二醇,三 (请先聞請背面之注意事填寫本頁) -裝 _ 0. I ! 線- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -18 - 4 6 7 9 4 3 經濟部中央操導局員工消費合作社印製 A7 _______B7_五、發明説明 丙二醇,卜乙氧基-2-丙醇,卜丁氧基_2一丙醇,卜丙氧 基-2-丙醇,丙二醇單甲基鍵,二丙二醇單甲基鱗,二丙 二醇單乙細,三丙二醇單乙基趟,三丙二醇單甲 ,和2-丁氧基乙醇。 以加速石夕土先驅物之水解而言,溶劑中添加水是有 利的。例如’當四乙氧基矽烷,四曱氧基矽烷,四丁氡 基矽烷,四丙氧基矽烷,四氯矽烷,或四溴矽烷,用為 石夕土先驅物時,水的存在以下面敘述的方式加速其水解 〇其他組成物 如本發明組合物,除了上述組成物之外,可以任擇 地包含其他組成物。 如本發明一個較佳的實施例,本發明組合物包含一 個折射率不超過2之材料。添加折射率不超過2之材料可 避免使用組合物表面的可見光之反射。 可加至本發明組合物,折射率不超過2之材料的實例 ,包括矽土(折射率U)。氧化錫(折射率1.0),碳酸釣( 折射率1· 6),氫氧化詞(折射率i. 6),碳酸韻(折射率u) ,碳酸錯(折射率U),白雲岩(折射率1.7),氟化妈(折 射率1.4),氟化鎂(折射率16),石英沙(折射率, 滿石(折射率’蒙脫石(折射率1‘5),高顏土(折射率 1』)’絹雲母(折射率16) ’氧化鐵(折射率18),和氧 化釔(折射率丨.9h 如本發明另一個較佳實施例,本發明組合物可再包 -I— JnJ I !| -- I -- H —i — t . (請先閲讀背面之注§k寫本頁) 訂 丨線---- -II —1— ·KpSiXq〇 (4_p) / 2 This paper size applies the Chinese National Standard (CNS) Α4 · 297 mm) (Please read the notes on the back first and fill in this page), ---------------- Order ------ line! Printed by the Consumers 'Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs _ 15-467943 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A 7 _B7__ V. Description of the Invention (13), where R represents optional hydrogen atoms and one or more One of the organic groups; X represents a thiol group or an i element atom; and p is a number satisfying 0 < p < 2 and q is a number satisfying 0 < q < 4. A preferred example of a precursor of a polysilicon coating that can be used in the composition of the present invention to form a silicon film is a hydrolyzable silane 4 derivative represented by the following chemical formula: RPSiVP, where R is as defined above; X represents alkane An oxygen or iS element atom; and p is 1 or 2. In this case, the organic functional machine represented by R is preferably an alkyl group (more preferably, an unsubstituted alkyl group having 1 to 18 carbon atoms, Most preferred is an alkyl group having 3 to 18 carbon atoms) or an aromatic group (preferably a phenyl group). Preferred specific examples of hydrolyzable silane derivatives include methyltrimethoxysilane, fluorenyltriethoxysilane, methyltripropoxysilane, fluorenyltributoxysilane, ethyltrimethoxy Silane, ethyltriethoxysilane, ethyltripropoxysilane, ethyltributoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltri'propoxysilane, Phenyltributoxysilane, difluorenyldimethoxysilane, dimethyldiethoxysilane, dimethyldipropoxysilane, dimethyldibutoxysilane, diethyldif emulsion Kimono fired 'diethyldiethoxy stone yakiya' diethyldipropoxysilane, diethyldibutoxysilane, phenylmethyldimethoxysilane, phenylmethyldiethoxy Silane, phenylmethyldipropoxysilane (please read the notes on the back ^^ write this page) Gutter This paper size is applicable to China National Standard (CNS) A4 (210 X 297 mm) 467943 Central Ministry of Economic Affairs A 7 __B7_ printed by the Bureau of Standardization, Shellfish Consumer Cooperative, V. Description of the invention (14), Phenylfluorenyldibutoxysilane, n-propyl Trimethoxysilane, n-propyltriethoxysilane, n-propyltripropoxysilane, n-propyltributoxysilane, γ-sugaroxypropyltrimethoxysilane, and γ-Acryloxypropyltrimethoxysilane 'Silane can be prepared by partially hydrolyzing a hydrolyzable silane derivative and then dehydrogenating by a polycondensation reaction, or by a partially hydrolyzed product of a hydrolyzable Shibaitane derivative It is prepared by dehydrogenation and polycondensation with partial hydrolysates of tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetrabutoxysilane, diethoxydimethoxysilane and other compounds. According to the following method, the silicone resin prepared by partial hydrolysis or dehydrogenation polycondensation of the aforementioned precursors is represented by the following average composition chemical formula: RpSiO (4-p) / 2 ⑴ where R is as defined above; X is an alkane Oxygen or! S prime atom; and p is a number satisfying 0 < ρ < 2. The content of the precursor of the composition of the present invention can be appropriately determined. For example, in terms of one part weight ratio of photocatalytic particles, the precursor is converted to silica content, and the upper limit of the content is preferably 10 parts by weight, more preferably 5 parts by weight, and most preferably 1 part. The lower limit of the content of the precursor is preferably 0.05 parts by weight, more preferably 0.1 part by weight, and most preferably 0.2 part by weight. Solvent The solvent of the composition of the present invention is not limited, as long as it can stably disperse the photocatalytic particles and precursors, and finally provide a hydrophilized surface (谙 read the note on the back first \ ^^ write this page) Order-line _ This paper size is applicable to China National Standard (CNS) A4 specification (210X297 mm) -17-467943 printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A7 --- _B7__ 5. Description of the invention (15). Examples of solvents that can be used herein include water, and organic solvents, and mixed solvents of water and organic solvents. Water, alcohols, or mixed solvents of water and alcohols are particularly preferred. The sum of the weight of the photocatalytic particles and the fine silica particles, or the weight of the precursor, is converted into silica, (this total content is called ', solid content ") is more than 0.01 to not more than 5% by weight of the composition of the present invention. The specific solids content can be measured by the following method. The composition (weight: A) is heated at 400 to 500 ° C for 3 hours to remove the liquid composition, the weight of the residue (weight: B) is measured, and the solid content is calculated according to the following equation: solid content (%) = (B / A ) X100 When the solid content exceeds 5% by weight, the composition surface may have a poor appearance due to fogging or dry edges. The upper limit of the solid content is preferably not more than by weight. When the solid content is less than 0.01% by weight, a hydrophilic surface may not be effectively obtained. The lower limit of the solid content is preferably a reset ratio of 0.05% by weight and 0.1% by weight. In the composition of the present invention, the amount of the solvent is such that the solid content of the photocatalytic particles and the precursors is within the above range. As a preferred embodiment of the present invention, the alcohol used has a molecular weight of 60 to 300, preferably It is 60 to 100 and is liquid at room temperature. Examples of preferred alcohols used herein include methanol, ethanol, n-propanol'isopropanol, tertiary butanol'isobutanol, n-butanol, 2-methylpropanol, pentanol, ethyl Glycol's monoacetone alcohol, diacetone alcohol, ethylene glycol monomethyl side, 4-light -4-methyl-2, pentamidine, dimalonase, propylene glycol, three (please note first please note on the back Please fill in this page)-Install _ 0. I! Line-This paper size is applicable to China National Standard (CNS) A4 (210X297 mm) -18-4 6 7 9 4 3 Preparation of A7 _______B7_ V. Description of the invention Propylene glycol, Buethoxy-2-propanol, Bubutoxy_2 monopropanol, Bupropoxy-2-propanol, Propylene glycol monomethyl bond, Dipropylene glycol monomethyl Base scale, dipropylene glycol monoethyl ether, tripropylene glycol monoethyl ester, tripropylene glycol monomethyl, and 2-butoxyethanol. In terms of accelerating the hydrolysis of Shixue precursors, it is advantageous to add water to the solvent. For example, when tetraethoxysilane, tetramethoxysilane, tetrabutylfluorenylsilane, tetrapropoxysilane, tetrachlorosilane, or tetrabromosilane are used as precursors of celite, the presence of water is described below The method accelerates its hydrolysis. Other components, such as the composition of the present invention, may optionally contain other components in addition to the above-mentioned composition. According to a preferred embodiment of the present invention, the composition of the present invention comprises a material having a refractive index of not more than two. Adding a material with a refractive index of not more than 2 can avoid the reflection of visible light on the surface of the composition. Examples of materials which can be added to the composition of the present invention with a refractive index not exceeding 2 include silica (refractive index U). Tin oxide (refractive index 1.0), carbonic acid fishing (refractive index 1.6), hydroxide word (refractive index i. 6), carbonic acid rhyme (refractive index u), carbonic acid (refractive index U), dolomite (refractive index 1.7), fluorinated mother (refractive index 1.4), magnesium fluoride (refractive index 16), quartz sand (refractive index, full stone (refractive index 'montmorillonite (refractive index 1'5)), high-yielding soil (refractive index 1 ”) 'sericite (refractive index 16)' iron oxide (refractive index 18), and yttrium oxide (refractive index 丨 .9h) According to another preferred embodiment of the present invention, the composition of the present invention may be repackaged-I- JnJ I! |-I-H —i — t. (Please read the note on the back §k first to write this page) Order 丨 -------- II—1— ·

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HH II -19 - 經濟部中央標準局員工消費合作社印製 467943 A7 五、發明説明(17) --- 含界面活性劑。添加界面活性劑,甚至在塗上組合物後 ’也可使元件表面立刻提高親水性和防霧性。特別的, 當依照本發明組合物含有_時,添加界面活性劑是較 好的。在祕情況下’應用本發明組合物後,需要幾個 小時以義表Φ之光親水化。在料候,本發明組合物 的醇類殘留於表面,表面之親水化常會不理想,直到光 催化劑進行親水化。添加界面活性劑,即使是元件應用 組合物後,可使表面親水化情況理想,也可以立刻提供 防霧性《另外再添加界面活性劑更可使本發明組合物均 勻應用至元件表面。 如本發明一個較佳的實施例,界面活性劑之添加量 要少於10份重量比,更佳的是約0312份重量比’相對 於一份光催化顆粒重量比。 可用於本發明組合物界面活性劑的實例包括陽離子 界面活性劑,如聚氧乙烯烷基苯基醚磺酸銨,聚氧乙烯 烧基苯基醚續酸納’脂肪酸鈉肥皂,脂肪酸鉀肥皂,二 辛基硫破珀酸納,燒基硫酸醋,烧基謎硫酸I旨,烧基硫 酸鈉,烧基醚硫酸納’聚氧乙烯烧基趟硫酸醋,聚氧乙 烯烷基醚硫酸鈉,烷基硫酸酯TEA鹽,聚氧乙烯烷基醚硫 酸酯TEA鹽,2-乙基己基烷基硫酸鈉,乙醯甲基牛續酸鈉 ’月桂酸醢曱基牛確酸納,苯續酸納十二院基苯續酸酯 ,月桂基硫琥珀酸二鈉,月桂基聚氧乙烯硫琥珀酸二鈉 ,聚羧酸,油醯基肌胺酸,胺醯醚硫酸酯,月桂酸醯肌 胺酸酯,和硫-FA酯納鹽;非離子界面活性劑,如聚氧乙 本紙張尺度通用中國國家標準(CNS > Μ規格(210 X 297公嫠) (請先閣讀背面之注意事很ί%窝本頁)HH II -19-Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 467943 A7 V. Description of the Invention (17) --- Contains surfactants. Adding a surfactant, even after the composition is applied, can immediately improve the hydrophilicity and anti-fogging property of the device surface. In particular, when the composition according to the present invention contains _, it is better to add a surfactant. In mysterious cases', after applying the composition of the present invention, it takes several hours to hydrophilize with light of the meaning Φ. As expected, the alcohols of the composition of the present invention remain on the surface, and the hydrophilization of the surface is often unsatisfactory until the photocatalyst is hydrophilized. Adding a surfactant, even after the composition is applied to the device, can make the surface hydrophilic, and it can provide anti-fogging immediately. In addition, adding the surfactant further allows the composition of the present invention to be evenly applied to the surface of the device. According to a preferred embodiment of the present invention, the surfactant is added in an amount of less than 10 parts by weight, more preferably about 0312 parts by weight 'relative to one part of the photocatalytic particles. Examples of surfactants that can be used in the composition of the present invention include cationic surfactants, such as polyoxyethylene alkylphenyl ether ammonium sulfonate, polyoxyethylene alkylphenyl ether, sodium sodium fatty acid soap, potassium fatty acid soap, Sodium dioctylthiocarbamate, sodium sulphate, sodium sulphate, sodium sulphate, sodium sulphate, polyoxyethylene sodium sulphate, polyoxyethylene alkyl ether sulphate, TEA salt of alkyl sulfate, TEA salt of polyoxyethylene alkyl ether sulfate, sodium 2-ethylhexyl alkyl sulfate, sodium acetomethylmethyltaurate, sodium laurate, sodium tallowate, benzoic acid Na-dodecyl benzoate, disodium lauryl thiosuccinate, disodium lauryl polyoxyethylene thiosuccinate, polycarboxylic acid, oleyl sarcosinate, amine ether sulfate, laurate Urethane, and thio-FA ester sodium salt; non-ionic surfactants, such as polyoxyethylene paper size Common Chinese National Standards (CNS > M specifications (210 X 297 cm)) (Please read the note on the back first (Things are very low on this page)

-20 - 467943 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(18 ) 烯月桂基醚,聚氧己稀三發基鍵,聚氧乙烯十六碳基醚 ,聚氧乙烯硬脂基醚,聚氧乙烯油基醚,聚氧己烯烷基 醚,聚氧乙烯烷基酯類,聚氧乙烯烷基酚醚,聚氧乙烯 壬基苯基醚,聚氧乙烯辛基苯基醚,聚氧乙烯月桂酸酯, 聚氧乙烯硬脂酸酯,聚氧乙烯烷基苯基醚,聚氧乙烯油 酸酯,山梨糖醇酐烷基酯,聚氧乙烯山梨糖醇酐烷基酯 類,聚醚-改性聚矽,聚酯-改性聚矽,山梨糖醇酐月桂 酸酯,山梨糖醇酐硬脂酸酯,山梨糖醇酐棕櫚酸酯,山 梨糖醇酐油酸酯,山梨糖醇酐半油酸酯,聚氧乙烯山梨 糠醇酐月桂酸酯,聚氧乙烯山梨糖醇酐硬脂酸酯,聚氧 乙烯山梨糖醇酐棕櫚酸酯,聚氡乙烯山梨糖醇酐油酸酯 ,甘油硬脂酸酯,聚甘油脂肪酯,烷基烷醯基胺醯,月 桂酸二乙醇胺醯,油酸二乙醇胺醯,氧乙烯十二烷基胺 ,聚氧乙稀十二院基1胺,聚氧乙婦烧基胺,聚氧乙婶八 癸基胺,聚氧乙烯烷基丙二胺,聚氧乙烯氧丙醯嵌段聚 合物,及聚氧二乙烯硬脂酸酯;兩性界面活性劑,如二 曱基烷基甜菜鹼,烷基離胺酸,胺醯甜菜鹼,及嘧唑林 ;和陰離子界面活性劑,如八癸基二曱基苯曱基氯化銨 ,烷基二甲基笨曱基氣化銨,四癸基二甲基苯曱基氯化 銨,二油酸基二曱基氣化銨,1-羥基乙基-2-烷基嘧唑林 四級鹽,烷基溴化異奎林,聚合胺,八癸基三甲基氯化 銨,烷基三曱基氯化銨,十二烷基三曱基氣化銨,六癸 基三曱基氣化銨,二十二烷基三甲基氯化銨,烷基嘧唑 林四級鹽,二烷基二曱基氯化銨,八癸基胺乙酸酯,四 本紙張尺度適用中國國家標準_( CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事^^寫本買)-20-467943 Printed by A7 B7, Consumer Cooperatives of the Central Bureau of Standards, Ministry of Economic Affairs 5. Description of the Invention (18) Ethylene lauryl ether, polyoxyhexyl triple bond, polyoxyethylene cetyl ether, polyoxyethylene hard Aliphatic ether, polyoxyethylene oleyl ether, polyoxyhexene alkyl ether, polyoxyethylene alkyl esters, polyoxyethylene alkyl phenol ether, polyoxyethylene nonylphenyl ether, polyoxyethylene octylbenzene Ether, polyoxyethylene laurate, polyoxyethylene stearate, polyoxyethylene alkylphenyl ether, polyoxyethylene oleate, sorbitan alkyl ester, polyoxyethylene sorbitan Esters, polyether-modified polysilicone, polyester-modified polysilicone, sorbitan laurate, sorbitan stearate, sorbitan palmitate, sorbitan oil Acid esters, sorbitan hemioleate, polyoxyethylene sorbitan anhydride laurate, polyoxyethylene sorbitan stearate, polyoxyethylene sorbitan palmitate, polyethylene sorbitan Alcoholic anhydride oleate, glyceryl stearate, polyglyceryl fatty ester, alkyl alkyl fluorenylamine hydrazone, laurate diethanolamine hydrazone, Acid diethanolamine hydrazone, oxyethylene dodecylamine, polyoxyethylene dodecyl 1 amine, polyoxyethenyl amine, polyoxyethylene octadecylamine, polyoxyethylene alkylpropanediamine, Polyoxyethylene oxypropylammonium block polymer, and polyoxydiethylene stearate; amphoteric surfactants such as diamidoalkyl betaine, alkyl lysine, amine betaine, and pyrazoline ; And anionic surfactants, such as octadecyl difluorenyl phenyl ammonium chloride, alkyl dimethyl benzyl ammonium vaporized ammonium, tetradecyl dimethyl phenyl ammonium chloride, dioleate Diammonium vaporized ammonium, 1-hydroxyethyl-2-alkylpyrazolium quaternary salt, alkyl isobrulin bromide, polymeric amine, octadecyltrimethylammonium chloride, alkyltriamyl Ammonium chloride, dodecyltrimethylammonium gasified ammonium, hexadecyltrimethylammonium gasified ammonium, behenyltrimethylammonium chloride, alkylpyrazolium quaternary salt, dialkyldiamine Fluorenyl ammonium chloride, octadecylamine acetate, four paper sizes are applicable to the Chinese national standard _ (CNS) A4 size (210X297 mm) (Please read the notes on the back first ^^ buy this)

-21 - 4 6 7 9 4 3 Α7Β7 經濟部中央標準局貝工消費合作社印裝 五、發明説明(19 ) 癸基胺乙酸酯,烷基丙二胺乙酸酯,和二癸基二甲基氣 化銨。 如本發明一個較佳的實施例,本發明組合物包含一 種酸。添加酸可增加使用本發明組合物之表面的極性, 使其即使在黑暗處也能維持良好親水性。 可添加至本發明組合物的酸之實例包括,能提高極 性的酸,如硝酸,硫酸,鹽酸,醋酸,丙酸,順—丁烯 二酸,己二酸,反—丁烯二酸,苯二酸,戊酸,乳酸, 丁酸’林檬酸’蘋果酸,苦味酸,甲酸,碳酸,和紛。 這些之中,硝酸,鹽酸,和硫酸是特別好的。 如本發明另一個較佳的實施例,本發明組合物包含 石夕烧水解之催化劑。當本發明組合物先驅物應用於表面 時’此催化劑以下面描述之方法加速石夕燒之水解。較佳 的催化劑實例包括硝酸,硫酸,鹽酸,醋酸,丙酸,順 —丁烯二酸,己二酸,反—丁烯二酸,笨二酸,戊酸, 乳酸,丁酸,棒檬酸’蘋果酸,苦味酸,曱酸,碳酸, 和酚’以上各酸之pH為2至5。 , 如本發明一個較佳的實施例,當矽土之先驅物為矽 醇時,本發明組合物包含矽醇聚合硬化催化劑。此催化 劑的存在,使本發明組合物在應用時,以下面描述之方 法加速矽醇的聚合反應可用於此處之催化劑較佳的實 例包括鋁化合物,如鋁螯合物,乙醯基醋酮酸鋁,過氯 酸鋁’氯化鋁,異丁氧鋁,及異丙氧鋁;鈦化合物,如 四異丙基鈦酸酯,及四丁基鈦酸酯;鹼性化合物,如氫 (請先閲讀背面之注意事寫本頁) 裝. 訂 .線 本紙張尺度適用中國國家揉準(CNS ) A4规格(210X 297公釐) 4 6 7 9 4 3 經濟部中央標準局員工消費合作社印製 Α7 Β7 五、發明説明(2〇 ) 氧化鋰,氫氧化鈉,氫氧化鉀,甲氧基鈉,乙酸鈉,曱 酸鈉,乙酸鉀’甲酸鉀,丙酸鉀,四曱基氯化銨,和四 f基氫氧化鞍;胺類化合物,如正-己胺,三丁基胺,二 但十一碳雙環,乙烯二胺,己烷二胺,二乙烯三胺,四 乙烯五胺’三己烯四胺’乙醇胺,γ_胺丙基三曱氧基矽 烷’ γ-胺丙基三甲氧基矽烷,γ-胺丙基曱基二曱氧基矽烷 ’ γ -(2-胺乙基)-胺丙基三Τ氧基石夕貌,及γ-(2-胺乙基)-胺丙基甲基_ —曱氧基發貌,锡化合物,如乙酿基醋嗣酸 錫’及一丁基辛酸錫;含金屬化合物,如辛酸録,乙隨 基醋酮酸鈷,及乙醯基醋酮酸鐵;和酸性化合物,如構 酸,硝酸,苯二酸,對-苯甲磺酸,及三氯乙酸。 如本發明一個較佳的實施例,本發明組合物包含一 個均質劑,使其應用於元件表面時可得到平滑的表面。 當本發明組合物應用於大物件時,添加均質劑是特別有 利的。較佳的均質劑實例包括二丙酮醇,乙二醇單甲基 醚’ 4-羥基-4-甲基-2-戊酮,二丙二醇,三丙二醇,1一 乙氧基-2-丙醇’ 1-丁氧基-2-丙醇,丙二醇單甲基醚,1— 丙氧基-2-丙醇,二丙二醇單曱基醚’二丙二醇單乙基醚 ,及三丙二醇單甲基醚. 如本發明一個較佳的實施例,本發明組合物更包含 一個抗菌金屬(如,銀,銅,或辞)或該金屬化合物。添 加上述金屬,可在本發明組合物應用於元件表面時,殺 死元件表面之細菌。另外,在組合物應用於元件上之後 ’可抑制表面上微生物,如霉菌’藻類’和苔蘚的生長 本紙張尺度適用中國國家標準(CNS ) Α4規格(210x29?公董) (諳先閱讀背面之注意事13^填寫本頁) .裝. 訂 -23 - 4 6 7 9 4 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(21 ) 0 另外,如本發明一個較佳的實施例,本發明組合物 更包含至少一個鉑族金屬,該金屬係擇自鉑,铑,釕, 锇,和銥所組成之族者。已知含金屬氧化物光催化劑的 表面,因為光催化劑的氧化性分解活性,而具有抗污性 ,抗菌性和除臭的功能.使用本發明組合物的元件表面 保留了此活性,上述金屬加強光催化劑之氧化性分解活 性,而增進抗菌性,除臭性,氣體分解性,有機物分解 性和其他表面的性質。 當儲存於錫罐,或内塗金屬之容器,或當應用至金 屬元件時’本發明組合物較佳的是弱酸性,中性或鹼性 。特別地’當上述實施例中添加酸時,較佳的是加入一 個pH調節劑。 另外,為了增進其中所含固體組成物之分散性,以 增進組合物之儲存穩定度’本發明組合物可任擇地包含 一個酸或驗。另外,如杲需要,可另外包含,色素,染料 ,儲存安定劑等等。 本發明组·合物龐用於元件表面 本發明組合物應用於欲改善親水性或防霧性之元件 表面,然後乾燥或硬化而形成薄膜。 如上所述,較佳的,本發明組合物最後得到元件上 的溥膜厚度不超過0. 4 μιη,較佳的不超過〇 _ 2 μιη。為了形 成此薄膜,應用於元件表面的本發明組合抽,其範圍較 佳的是約1 X 1〇_4至20mg/cm2,更佳的是約5X 10-4至lmg/cm2 本紙張尺度適用中國國家標準(CNS ) M规格(210X297公釐) ϋ I - - - - -- H ft ί -* · / (諳先閱讀背面之注意事$4、填寫本頁) --β 24 " 467943 經濟部中央標準局員工消費合作社印製 A7 _____B7____五、發明説明(22 ) 0 本發明組合物可用任何適當的方法應用至元件表面 ,適當方法的實例包括喷霧塗層,浸潰塗層,澆流塗層 ’滾旋塗層,滾動塗層,塗刷塗層,和泡沫塗層。 多且合物應用至元件表面後,經過乾燥或硬化而形成 薄膜。此處使用'、乾燥或硬化"意思是,本發明組合物所 含之矽土先驅物或聚矽先驅物轉換成為矽土或聚矽。因 此’乾燥方式可以採用空氣乾燥或加熱乾燥。另外,紫 外光照射等可誘引聚合反應,使先驅物轉換為矽土或聚 如本發明一個較佳的實施例,本發明組合物的供應 法是’填充於一個噴霧容器内,使使用者適當地將本發 明組合物應用至元件表面》 第1圖顯示一個適合填充本發明組合物之噴霧容器 。容器架構(1)較好是鋁製品重量輕,容易操作,而且穩 固。然而’也可以使用硬鋁,銅-鋁合金,鈦合金,不銹 鋼等。 當本發明组合物為酸性,最好使用抗酸樹脂襯層(2) ’避免金屬容器架構(1)與酸性組合物直接接觸。此處使 用之抗酸襯層包括襯層ABS樹脂,聚碳酸,甲基戊烯樹脂 ’聚氣乙烯,聚丙烯,聚乙烯,四氟乙烯樹脂,乙烯丙 烯氟化物’氯乙烯三氟樹脂,二氟乙烯樹脂,烷氧基過 氟化物樹脂,酚樹脂,環氧樹脂,聚丙烯樹脂,聚醚氣 化物,聚石風,聚苯乙烯,聚苯醚,聚硫苯,聚亞胺, (讀先閲讀背面之注意事^^寫本頁) .裝· Η 訂 線. 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) -25 - 46 7 943 經濟部中央標準局員工消費合作社印製 Μ _______Β7 五、發明説明(23 ) 尼龍,及離聚物襯層。第1圖顯示之容器内,上方有一 可移動之蓋罩,顯示於第2圖。此蓋罩包含;一個管子(幻 將本發明組合物引至排出部份;一個排出口(4); 一個壓 柃(5) ’其上端置於罩框(12)上方,以便於用指頭壓線圈 彈皆(6)’個橡勝(9),一個山型蓋罩(1〇); 一個封片(11) 於山型蓋罩(10)與容器架構α)接合處;及一個罩框(12) 。壓桿(5)内部有一個孔以引導本發明组合物至排出部份 。在排出口(4)上方有一個傳輸口(7),和一個傳輸口(8) 引向橡膠(9)。 因此,壓下壓桿(5)之前,傳輸口(?)並未接觸排出 口(4),而傳輸口(8)以橡膠封住,避免組合物送出。壓 下壓桿(5)後,傳輸口(8)置於壓桿(5),組合物由管子(3) 引導至壓杯(5)與罩框(12)之間的空間,再引至壓桿(5) 内部的孔洞。同時,傳輸口(7)接於排出口(4),使得引 至壓桿(5)内部孔道的組合物經由排出口(4)送出。 較佳的,管子(3) ’壓桿(5),.排出口(4),和罩框(12) 内部均使用上述抗酸樹脂。 較佳的,橡膠(9)亦為抗酸橡膠,如,乙烯橡膠,丙 烯橡膠,或聚矽橡膠等等。 較佳的,排出口(4)略微向上傾斜。 另外,在壓桿(5)内部,接連排出口的孔洞可裝置一 個十子形凹槽或一個螺旋凹槽,使得組合物容易地引至 排出口。 其他喷霧容器實施例,第3圖和第4圖所顯示的雙層 (CNS) Α视格(2似297公整)— - n i H n I n .^1 --1 I _'. (請先閱讀背面之注意事^--'乂填寫本育) i 訂| 線_ _ 26 - 4 6 7 943 經濟部中央標準局員工消費合作社印裝 A7 B7 五、發明説明(24 ) — 谷斋結構疋很適用的。 第3圖顯示的構造内,第1圖容器内有一個内容器 (13),其中裝滿塗層液體樣品D11和推進劑氣體,如氮氣 ,:DEM’或LPG。此構造的優點是,即使是樹脂襯層有一 小孔,本發明組合物也不會進入而直接接觸金屬容器架 構⑴。 …、 第4圖顯示的構造中,圖丄顯示的容器内,有—個氣 球狀容器(14),具有抗壓性和良好的壓力傳動性,容器 底部有一個孔洞。此構造可使氣體和液體分別填入容器 相關的部位。例如,氣球狀容器(14)(圖人部份)填充本發 明组合物,而外容器間與氣球狀容器之空間(圖B部份)填 充氮氣。因此,可避免不利的情況,例如,氣體逐漸溶 入液體而造成容器内壓力的降低。 氮氣由容器底部填充,然後以橡膠塞(15)封住容器 之孔洞。這可使使用後殘留的壓力很容易地由移去橡膠 塞(15)而釋放,有利地提供其安全性。 聚乙婦,聚氯乙稀等具有抗塵性和塵力傳動性,適 合使用於氣球狀容器14構造。為了提高壓力傳動性採用 如第5圖(a)和(b)所顯示踏板狀不規則型是較佳的。 氮氣之外,醚類氣體,如二亞T醚,和惰性氣體, 如氬和氦,可作為填充氣體。 [實例] 本發明以下列實例做更詳細的說明,雖然它並不只 限於這些實例=> 本紙張尺度適用中國國家標準(CNS ) A4規格_( 21G x 297公廣) n· n J4^ ϋ In Hr --1 - 裝 『 - ί請先聞讀背面之注意事ikz填寫本頁) 1 .訂— 線 467943 A7 B7-21-4 6 7 9 4 3 Α7Β7 Printed by the Shellfish Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 5. Description of the invention (19) Decylamine acetate, alkylpropylenediamine acetate, and didecyldimethylamine Base gasified ammonium. According to a preferred embodiment of the invention, the composition of the invention comprises an acid. The addition of acid can increase the polarity of the surface on which the composition of the present invention is used, so that it can maintain good hydrophilicity even in dark places. Examples of the acid that can be added to the composition of the present invention include acids that increase polarity, such as nitric acid, sulfuric acid, hydrochloric acid, acetic acid, propionic acid, maleic acid, adipic acid, trans-butylene acid, benzene Diacid, valeric acid, lactic acid, butyric acid, linoleic acid, malic acid, picric acid, formic acid, carbonic acid, and phenol. Among these, nitric acid, hydrochloric acid, and sulfuric acid are particularly good. According to another preferred embodiment of the present invention, the composition of the present invention comprises a catalyst for the hydrolysis of slab fire. When the precursor of the composition of the present invention is applied to the surface ', this catalyst accelerates the hydrolysis of Shibaiyaki in the manner described below. Examples of preferred catalysts include nitric acid, sulfuric acid, hydrochloric acid, acetic acid, propionic acid, maleic acid, adipic acid, trans-butenedioic acid, azelaic acid, valeric acid, lactic acid, butyric acid, and citric acid 'Malic acid, picric acid, gallic acid, carbonic acid, and phenol' has a pH of 2 to 5. As in a preferred embodiment of the present invention, when the precursor of silica is silanol, the composition of the present invention includes a silanol polymerization hardening catalyst. The presence of this catalyst allows the composition of the present invention to accelerate the polymerization of silanol by the method described below. Preferred examples of the catalyst that can be used herein include aluminum compounds such as aluminum chelates, acetoacetone Acid aluminum, aluminum perchlorate 'aluminum chloride, aluminum isobutoxide, and aluminum isopropoxide; titanium compounds such as tetraisopropyl titanate, and tetrabutyl titanate; basic compounds such as hydrogen ( Please read the note on the back first and write this page) Binding, ordering, thread paper size is applicable to China National Standard (CNS) A4 (210X 297 mm) 4 6 7 9 4 3 Printed by the Consumers Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs Preparation A7 B7 V. Description of the invention (20) Lithium oxide, sodium hydroxide, potassium hydroxide, sodium methoxylate, sodium acetate, sodium acetate, potassium acetate 'potassium formate, potassium propionate, tetramethylammonium chloride , And tetrafyl saddle hydroxide; amine compounds, such as n-hexylamine, tributylamine, dibutecyl bicyclic ring, ethylene diamine, hexanediamine, diethylenetriamine, tetraethylenepentamine Trihexene tetramine 'ethanolamine, γ-aminopropyltrimethoxysilane' γ-aminopropyltrimethoxy Silane, γ-aminopropylfluorenyldimethoxysilane, γ- (2-aminoethyl) -aminopropyltritoxylate, and γ- (2-amineethyl) -aminopropylmethyl The appearance of alkoxide — tin compounds, such as tin ethyl acetate and monobutyltin octoate; metal compounds, such as octanoate, cobalt ethyl acetoacetate, and ethyl acetoacetone Ferric acid; and acidic compounds such as acid, nitric acid, phthalic acid, p-benzoic acid, and trichloroacetic acid. As a preferred embodiment of the present invention, the composition of the present invention contains a homogenizing agent, so that a smooth surface can be obtained when it is applied to the surface of a component. The addition of a homogenizer is particularly advantageous when the composition of the present invention is applied to a large object. Examples of preferred homogenizers include diacetone alcohol, ethylene glycol monomethyl ether '4-hydroxy-4-methyl-2-pentanone, dipropylene glycol, tripropylene glycol, 1-ethoxy-2-propanol' 1-butoxy-2-propanol, propylene glycol monomethyl ether, 1-propoxy-2-propanol, dipropylene glycol monofluorenyl ether 'dipropylene glycol monoethyl ether, and tripropylene glycol monomethyl ether. According to a preferred embodiment of the present invention, the composition of the present invention further comprises an antibacterial metal (such as silver, copper, or silicon) or the metal compound. The addition of the above metals can kill bacteria on the surface of the component when the composition of the present invention is applied to the surface of the component. In addition, after the composition is applied to the element, it can 'inhibit the growth of microorganisms on the surface, such as mold' algae 'and moss. The paper size is applicable to the Chinese National Standard (CNS) A4 size (210x29? Public director) (谙 read the first Note 13 ^ Fill in this page). Pack. Order-23-4 6 7 9 4 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (21) 0 In addition, as a better implementation of the present invention For example, the composition of the present invention further comprises at least one platinum group metal selected from the group consisting of platinum, rhodium, ruthenium, osmium, and iridium. It is known that the surface of a metal oxide-containing photocatalyst has antifouling, antibacterial, and deodorizing functions due to the oxidative decomposition activity of the photocatalyst. The surface of the element using the composition of the present invention retains this activity, and the above metal strengthens Photocatalyst's oxidative decomposition activity, and improve antibacterial, deodorizing, gas decomposing, organic decomposing and other surface properties. When stored in a tin can, or a container coated with metal, or when applied to a metal element, the composition of the present invention is preferably weakly acidic, neutral, or alkaline. In particular, when an acid is added in the above embodiment, it is preferable to add a pH adjuster. In addition, in order to improve the dispersibility of the solid composition contained therein to improve the storage stability of the composition ', the composition of the present invention may optionally contain an acid or a salt. In addition, if necessary, it can additionally contain pigments, dyes, storage stabilizers and the like. The composition and composition of the present invention is applied to the surface of a component. The composition of the present invention is applied to the surface of a component whose hydrophilicity or anti-fogging property is to be improved, and then dried or hardened to form a thin film. As described above, preferably, the thickness of the diaphragm film on the element finally obtained by the composition of the present invention does not exceed 0.4 μm, and preferably does not exceed 0 _ 2 μm. In order to form this film, the combination pump of the present invention applied to the surface of the element preferably has a range of about 1 X 10-4 to 20 mg / cm2, and more preferably about 5 X 10-4 to 1 mg / cm2. This paper size is applicable China National Standard (CNS) M Specification (210X297 mm) ϋ I-----H ft ί-* · / (谙 Please read the note on the back of $ 4, fill out this page) --β 24 " 467943 Economy Printed by the Consumer Standards Cooperative of the Ministry of Standards of the People's Republic of China A7 _____B7____ 5. Description of the Invention (22) 0 The composition of the present invention can be applied to the surface of the element by any suitable method. Examples of the appropriate method include spray coating, dip coating, pouring Flow coating's spin coating, roll coating, brush coating, and foam coating. After the multi-complex is applied to the surface of the device, it is dried or hardened to form a thin film. As used herein, ', drying or hardening' means that the silica precursor or polysilicon precursor contained in the composition of the present invention is converted into silica or polysilicon. Therefore, the 'drying method' can be air drying or heat drying. In addition, ultraviolet light irradiation can induce the polymerization reaction, so that the precursors are converted to silica or polymerized. A preferred embodiment of the present invention is to supply the composition of the present invention by 'filling in a spray container, so that the user can properly "Applying the composition of the invention to the surface of a component" Figure 1 shows a spray container suitable for filling the composition of the invention. The container structure (1) is preferably an aluminum product which is light in weight, easy to handle, and stable. However, it is also possible to use hard aluminum, copper-aluminum alloy, titanium alloy, stainless steel, and the like. When the composition of the present invention is acidic, it is preferable to use an acid-resistant resin liner (2) 'to avoid direct contact between the metal container structure (1) and the acidic composition. The acid-resistant lining used here includes lining ABS resin, polycarbonate, methylpentene resin 'polyethylene, polypropylene, polyethylene, tetrafluoroethylene resin, ethylene propylene fluoride' vinyl chloride trifluoro resin, two Fluoroethylene resin, alkoxy perfluoride resin, phenol resin, epoxy resin, polypropylene resin, polyether gasification, polylithic wind, polystyrene, polyphenylene ether, polythiobenzene, polyimide, (read Please read the notes on the back ^^ write this page). · · Binding line. This paper size is applicable to China National Standard (CNS) Α4 size (210X297 mm) -25-46 7 943 Staff Consumer Cooperatives, Central Bureau of Standards, Ministry of Economic Affairs Printing M _______B7 V. Description of the invention (23) Nylon and ionomer liner. The container shown in Figure 1 has a removable cover above it, which is shown in Figure 2. The cover contains: a tube (which guides the composition of the present invention to the discharge portion; a discharge port (4); a pressure pin (5) 'whose upper end is placed above the cover frame (12) to facilitate pressing with a finger The coil springs are all (6) 'oak wins (9), a mountain cover (10); a cover (11) at the junction of the mountain cover (10) and the container structure α); and a cover frame (12). The pressure lever (5) has a hole inside to guide the composition of the present invention to the discharge portion. Above the discharge port (4) there is a transfer port (7) and a transfer port (8) leads to the rubber (9). Therefore, before the pressure lever (5) is depressed, the transfer port (?) Does not contact the discharge port (4), and the transfer port (8) is sealed with rubber to prevent the composition from being sent out. After pressing down the pressing rod (5), the transmission port (8) is placed on the pressing rod (5), and the composition is guided by the tube (3) to the space between the pressing cup (5) and the cover frame (12), and then to Holes inside the lever (5). At the same time, the transmission port (7) is connected to the discharge port (4), so that the composition introduced to the inner channel of the pressure rod (5) is sent out through the discharge port (4). Preferably, the pipe (3), the pressing rod (5), the discharge port (4), and the inside of the cover frame (12) all use the above-mentioned acid-resistant resin. Preferably, the rubber (9) is also an acid-resistant rubber, such as ethylene rubber, propylene rubber, or silicone rubber, and the like. Preferably, the discharge port (4) is slightly inclined upward. In addition, inside the pressure rod (5), a hole in the discharge port can be provided with a ten-shaped groove or a spiral groove, so that the composition can be easily led to the discharge port. Other spray container embodiments, the double-layer (CNS) Α view grid (2 like 297 mm) shown in Figures 3 and 4-ni H n I n. ^ 1 --1 I _ '. ( Please read the notes on the back ^-'乂 Fill this education first) i Order | _ _ _ 26-4 6 7 943 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of Invention (24) — Gu Zhai Structure 疋 works well. In the structure shown in Fig. 3, there is an inner container (13) in the container of Fig. 1, which is filled with a coating liquid sample D11 and a propellant gas such as nitrogen: DEM 'or LPG. This structure has the advantage that even if the resin liner has a small hole, the composition of the present invention does not enter and directly contacts the metal container frame ⑴. …, In the structure shown in Figure 4, in the container shown in Figure 丄, there is a balloon container (14), which has pressure resistance and good pressure transmission, and there is a hole in the bottom of the container. This configuration allows gas and liquid to be filled into the relevant parts of the container separately. For example, the balloon-like container (14) (illustrated in the figure) is filled with the composition of the present invention, and the space between the outer container and the balloon-like container (part in Figure B) is filled with nitrogen. As a result, unfavorable conditions can be avoided, such as a gradual dissolution of the gas into the liquid and a decrease in the pressure in the container. Nitrogen is filled from the bottom of the container, and the hole of the container is sealed with a rubber stopper (15). This allows the pressure remaining after use to be easily released by removing the rubber stopper (15), which advantageously provides its safety. Polyethylene, polyvinyl chloride, etc. have dust resistance and dust transmission properties, and are suitable for use in the structure of a balloon-shaped container 14. In order to improve the pressure transmission, it is preferable to use a pedal-shaped irregular type as shown in Figs. 5 (a) and (b). In addition to nitrogen, ether-based gases such as diethylene ether, and inert gases such as argon and helium can be used as the filling gas. [Examples] The present invention will be described in more detail with the following examples, although it is not limited to these examples => This paper size applies the Chinese National Standard (CNS) A4 specifications_ (21G x 297 public broadcasting) n · n J4 ^ ϋ In Hr --1-Install 『-Please read the notes on the back ikz first and fill in this page) 1. Order — line 467943 A7 B7

經濟部中央棹準局員工消費合作社印製 用於下列實例之乳化欽溶勝組合物和取得方法記述 於後。 氧化鈦溶膠ST-K01 :由8份重量比氧化鈦(銳鈦礦)顆 粒,2份重量比烷基矽酸鹽,54.8份重量比硝酸水溶液, 28份重量比甲醇,和7.2份重量比丙醇組成之組合物:由Printed by the Consumers' Cooperatives of the Central Government Bureau of the Ministry of Economic Affairs and used in the following examples. Titanium oxide sol ST-K01: consists of 8 parts by weight titanium oxide (anatase) particles, 2 parts by weight alkyl silicate, 54.8 parts by weight aqueous nitric acid solution, 28 parts by weight methanol, and 7.2 parts by weight acrylic Composition consisting of alcohol:

Ishihara Sangyo Kaisha Ltd供應。 乳化敛溶膠ST-K03 .由5份重量比氧化鈦(銳鈦礦)顆 粒’ 5份重量比烷基矽酸鹽’ 54. 8份重量比硝酸水溶液, 28份重量比曱醇’和7· 2份重量比丙醇組成之纟且合物:由Supply by Ishihara Sangyo Kaisha Ltd. Emulsified sol ST-K03. From 5 parts by weight of titanium oxide (anatase) particles' 5 parts by weight of alkyl silicate '54.8 parts by weight of aqueous nitric acid solution, 28 parts by weight of methanol' and 7 · Hydrazone compound consisting of 2 parts by weight of propanol: consisting of

Ishihara Sangyo Kaisha Ltd供應。 氧化鈦溶膠TA-15 :由15份重量比氧化鈦(銳鈦礦)顆 粒和85份重量比硝酸水溶液組成之組合物:由Nissan Chemical Industries Ltd供應。 實例A1矽薄膜先驅物及溶劑用量 氧化鈦溶膠(ST-K01)以乙醇稀釋10倍,100倍或1〇〇〇 倍以製備樣品Al,A2和A3。樣品Al,A2和A3.之固體含量 分別為 lwt%,0. lwt%和0. Olwt%。 樣品放置3天。結果,沒有發生凝結情形= 樣品A1至A3層塗於一個10平方公分鈉鈣玻璃基質, 該塗層於室溫乾燥18小時。 結果,所有樣品都得到透明而且均勻的塗層。樣品A1 塗層可看到干擾邊緣。 接著,各塗層以光源(BLB (black light blue)螢光 燈,Sankyo Denki製造),其紫外光照射強度為〇· 25mW/cm2 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) {請先聞讀背面之注意事%寫本頁} P· -訂- .線 -28 - 經濟部中央標準局員工消費合作社印製 4 6 7 9 4 3 A7 B7 五、發明説明(.26 ) 光線照射一小時。然後,評估塗層防霧性。評定標準如 下。 ◎:於層塗的玻璃吹氣,結果未起霧。 〇:於層塗的玻璃吹氣,結果略起霧,但仍可透過 層塗的玻璃清楚地看到影像。 A:於層塗的玻璃吹氣,結果起霧,而無法透過層塗 的玻璃清楚地看到影像,雖然比起基質玻璃本身,起霧 情況並不嚴重。 X:於層塗的玻璃吹氣,結果與基質玻璃本身產生者 比較,有起霧現象。 至於防霧性,樣品A1和A2評定為◎,而樣品A3為X。 評估樣品A1之塗層對基質的黏著性和塗層由基質的 剝離性。這種情形下,為評估塗層對基質的黏著性,浸 水之Kimwipe滑過塗層,並測定從基質剝離塗層所需滑過 的次數。塗層對基質的黏著性以滑過的次數評估。另外 ,為評估塗層由基質的剝離性,以塑膠擦子滑過塗層, 並測定從基質剝離塗層所需滑過的次數。塗層由基質的 剝離性以滑過的次數評估。每一個測試均重複三次。 結果,塗層對基質的黏著性方面,滑過的動作重複20 次,而無剝離現象發生。另外,塗層由基質的剝離性方 面,滑過的動作2至3次,使得塗層完全由基質剝離。 實例A2 添加銅 硫酸銅水溶液(ΙΟΟμΙ),其中之銅濃度為lg/liter,加至 10g氧化鈦溶膠(ST-K01),該混合物以乙醇稀釋100倍。 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -29 - ^^^^1 ^^^^1 ^^^^1 ^^^^1 ^^^^1 ^^1 -.- 03. (請先鬩讀背面之注意事項-r,%寫本頁)Supply by Ishihara Sangyo Kaisha Ltd. Titanium oxide sol TA-15: A composition consisting of 15 parts by weight of titanium oxide (anatase) particles and 85 parts by weight of an aqueous nitric acid solution: supplied by Nissan Chemical Industries Ltd. Example A1 Precursor of Silicon Film and Amount of Solvent Titanium oxide sol (ST-K01) was diluted 10 times, 100 times or 1000 times with ethanol to prepare samples Al, A2 and A3. Olwt%。 Samples Al, A2 and A3. Have a solid content of lwt%, 0.1 wt% and 0.1 wt%, respectively. The samples were left for 3 days. As a result, no coagulation occurred = the layers of samples A1 to A3 were applied to a 10 cm² soda-lime glass substrate, and the coating was dried at room temperature for 18 hours. As a result, all samples obtained a clear and uniform coating. Interference edges can be seen on the sample A1 coating. Next, each coating uses a light source (BLB (black light blue) fluorescent lamp, manufactured by Sankyo Denki), and its ultraviolet light irradiation intensity is 0.25 mW / cm2. The paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm). ) {Please read the notes on the back of the page% to write this page} P · -Order- .Line-28-Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 4 6 7 9 4 3 A7 B7 V. Description of Invention (.26 ) The light shines for an hour. Then, the anti-fogging property of the coating was evaluated. The evaluation criteria are as follows. :: The layer-coated glass was blown, and as a result, it was not fogged. 〇: The layer-coated glass is blown, and the result is slightly fogged, but the image can be clearly seen through the layer-coated glass. A: Blowing on the layer-coated glass results in fogging, but the image cannot be clearly seen through the layer-coated glass, although the fogging is not serious compared to the matrix glass itself. X: The layer-coated glass is blown. As a result, compared with the producer of the matrix glass, there is a fogging phenomenon. As for the anti-fogging property, samples A1 and A2 were rated as ◎, and sample A3 was X. The adhesion of the coating of the sample A1 to the substrate and the peelability of the coating from the substrate were evaluated. In this case, in order to evaluate the adhesion of the coating to the substrate, a immersed Kimwipe slipped over the coating and the number of times it was necessary to peel off the coating from the substrate was measured. The adhesion of the coating to the substrate was evaluated by the number of slips. In addition, in order to evaluate the peelability of the coating from the substrate, a plastic wiper was used to slide over the coating, and the number of slips required to peel the coating from the substrate was measured. The coating was evaluated by the peelability of the substrate by the number of slips. Each test was repeated three times. As a result, in terms of the adhesion of the coating to the substrate, the sliding motion was repeated 20 times without peeling. In addition, the coating is peeled from the substrate by the sliding action of the substrate 2 to 3 times. Example A2 A copper copper sulfate aqueous solution (100 μl) was added, in which the copper concentration was lg / liter, to 10 g of a titanium oxide sol (ST-K01), and the mixture was diluted 100-fold with ethanol. This paper size applies to China National Standard (CNS) A4 specification (210 × 297 mm) -29-^^^^ 1 ^^^^ 1 ^^^^ 1 ^^^^ 1 ^^^^ 1 ^^ 1-. -03. (Please read the notes on the back -r,% write this page)

、1T 線 經濟部中央標準局貞工消費合作社印製 4 6 7943 A7 . B7 五、發明説明(27 ) 稀釋的液體靜置3天。結果,未產生凝結現象,這個良好 分散性的結果顯示,以銅為抗菌金屬添加至塗層液體, 不會影響塗層液體的操作,所以塗層液體可以如實例1來 應用。 實例A3 添加矽土 氧化鈦溶膠(TA-15)以乙醇稀釋,製備塗層液體,其 中氧化钦顆粒之濃度為0.5%重量比。 另外,氧化鈦溶膠(TA-15)與矽土溶膠("Glasca A," 平均顆粒直徑為 10 nm ’ Japan Synthet i c Rubber Co.,Ltd. 製造)混合,該混合物以乙醇稀釋,以製備塗層液體,其 中氧化鈦顆粒之濃度為0. 5%重量比,而矽土顆粒之濃度 為0. 5%重量比。 各塗層液體層塗到一個10平方公分鈉鈣玻璃基質, 該層塗基質置於50°C—小時,後靜置15分鐘,以使層塗基 質冷卻,得到樣品A4和A5。 檢查樣品A4和A5之塗層。結果,樣品A4,塗層高度 反射可見光,且有閃光,而樣品A5,塗層基本上不反射 可見光,而具有良好的可見光穿透性。 另外,樣品A4和A5以紫外光照射強度為0. 25 mW/cm2 之光源(BLB螢光燈)光線照射2小時。評估塗層防霧性。 結果,兩個樣品,以如實例A1防霧性之評估法,均具有 良好防霧性(©)。 上述的結果顯示,添加折射率比鈥小之矽土,可使 塗層具有優良的防霧性,而能保留表面之可見光穿透性 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -30 - (請先閣讀背面之注意事寫本頁)Line 1T Printed by Zhengong Consumer Cooperative, Central Bureau of Standards, Ministry of Economic Affairs 4 6 7943 A7. B7 V. Description of the invention (27) The diluted liquid is left to stand for 3 days. As a result, no coagulation occurred. The result of good dispersibility shows that the addition of copper as the antibacterial metal to the coating liquid does not affect the operation of the coating liquid, so the coating liquid can be applied as in Example 1. Example A3 Silica was added. Titanium oxide sol (TA-15) was diluted with ethanol to prepare a coating liquid, in which the concentration of oxidized particles was 0.5% by weight. In addition, titanium oxide sol (TA-15) was mixed with silica sol (" Glasca A, " average particle diameter is 10 nm 'made by Japan Synthet ic Rubber Co., Ltd.), and the mixture was diluted with ethanol to prepare 5% 重量 比。 The coating liquid, wherein the concentration of titanium oxide particles is 0.5% by weight, and the concentration of silica particles is 0.5% by weight. Each coating liquid layer was applied to a 10 cm 2 soda-lime glass substrate. The coating substrate was placed at 50 ° C. for one hour, and then allowed to stand for 15 minutes to cool the coating substrate to obtain samples A4 and A5. Inspect samples A4 and A5 for coating. As a result, the sample A4, the coating highly reflects visible light and has a flash, while the sample A5, the coating substantially does not reflect visible light and has good visible light permeability. In addition, the samples A4 and A5 were irradiated with light from a light source (BLB fluorescent lamp) having an intensity of 0.25 mW / cm2 for 2 hours. Assess coating anti-fog properties. As a result, both samples had good anti-fogging properties in the evaluation method of anti-fogging properties as in Example A1 (©). The above results show that the addition of silica with a refractive index lower than that can make the coating have excellent anti-fogging properties while retaining the visible light transmittance of the surface. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297). PCT) -30-(Please read the note on the back to write this page)

467943 A7 經濟部中夬標隼局員工消費合作社印製 B7五、發明説明(.28 ) 〇 實例A4 添加界面活性劑 氧化鈦溶朦(TA-15)與妙土溶耀"("Glasca A")混合, 該混合物以乙醇稀釋,以製備塗層液體,其中之氧化鈦 顆粒濃度為0.5%重量比,而矽土顆粒濃度為0.5%重量比 〇 氧化欽溶膠(TA-15)與石夕土溶膠(M Glasca AM)和界面 活性劑聚乙二醇(分子量3000)混合,該混合物以乙醇稀 釋,以製備塗層液體,其中之氧化鈦顆粒濃度為0.5%重 量比,矽土顆粒濃度為0.5%重量比,而聚乙二醇濃度為0.2 重量比。 氧化鈦溶膠(TA-15)與矽土溶膠("Glasca A")和改性 聚石夕(KF-351,聚崎型,The Shin-Etsu Chemical Co. ,Ltd. 製造)混合,該混合物以乙醇稀釋,以製備塗層液體,其 中之氧化鈦顆粒濃度為(].5%重量比,矽土顆粒濃度為0. 5% 重量比,而改性聚石夕濃度為0. 2重量比。 另外,氧化鈦溶膠(TA-15)與矽土溶膠("Glasca A") 和改性聚石夕(KF-945 ’ 聚醚型,The Shin-Etsu Chemical Co. ,Ltd.製造)混合,該混合物以乙醇稀釋,以製備塗層液 體,其氧化鈦顆粒濃度為0.5%重量比,矽土顆粒濃度為 0.5%重量比,而改性聚矽濃度為0.2重量比。 各塗層液體層塗至10平方公分鈉鈣玻璃基質,該層 塗基質置於50。(:一小時,後靜置15分鐘以使層塗基質冷卻 ,得到樣品A6至A9。 (請先閲讀背面之注意事項疒4寫本頁) -裝- 訂· 線 本紙張尺度適用中國國家標準(CNS ) A4規格(2ίΟΧ297公釐) -31 - 4 6 7 9 4 3 A7 B7 五、發明説明(29 ) 樣品A6至A⑽紫外統㈣度狀25 mW/Gm2之光源 (BLB螢光燈)光線照射,以測定塗層防霧性和以光線照射 時間為函數的變化圖。其結果顯示於圖6。 特別地,樣品A6,照射2小時後具有良好的防霧性( ◎ ) 3另外,樣品A7得到良好防霧性的照射時間(◎)是3 小時,樣品A8是4小時,而樣品A9不少於2〇小時’其結果 顯示添加界面活性劑,其疏水性影響較強者需要更長的 紫外光照射時間’才可以得到防霧性。 界面活性劑之添加量 氧化鈦溶膠(TA-15),矽土溶膠("Glasca a"),含聚氧乙 烯對-烷基笨基醚(Penerole,NP-95,Matsumoto Yushi 製 造)之非離子界面活性劑,和乙醇混合,以製備塗層液體 樣品B1至B4,該等樣品包含氧化鈦顆粒,矽土顆粒,和界 面活性劑分散於溶劑中, (請先閲讀背面之注意事寫本頁;> -裝_ -訂 經濟部中央樣準局員工消費合作社印製 樣品 氧化鈦(健量比) 较土顆粒(份道量比) 介而活性劑(份重量比) Β1 50 25 0 Β2 50 25 20 Β3 50 25 so Β4 50 25 1〇〇 塗層液體樣品Β1至Β4分別層塗至鈉鈣玻璃基質,塗 層乾燥’再以紫外光照射強度為0.25 mW/cm2之光源(black light blue (BLB螢光燈),Sankyo Denki製造)光線照射 ’以測定塗層防霧性和以光線照射時間為函數的變化圖 。其結果顯示於圖7 ^另外,以如實例A1評定標準評估防 霧性。 本紙張尺度適用中_家標準(CNS ) A4規格(2mx297公楚) 線. • frr 二* /94 3 Α7 87 五、發明説明(3〇 ) 如圖7所顯示,不論紫外光照射多長時間,基質玻璃 基本上都只表現X級防霧性’然而,在紫外光照射5〇小時 後’所有塗層液體樣品B1至B4塗層之樣品,其基質玻璃 表面展現良好的防霧性(◎)。 塗層液體樣品Β1塗層之樣品在紫外光照射之前,完 全未展現防霧性,而塗層液體樣品Β2至Β4塗層之樣品在 紫外光照射前和後均展現防霧性。 塗層液體樣品Β1塗層之樣品不具起始防霧性的原因 ’被認為是乙醇殘留於塗層内。增加照射時間而得到防 霧性’可能是因為光催化劑之光激反應分解乙醇。 相反的,摻有界面活性劑之塗層液體樣品Β2至Β4製 備之樣品’是因為界面活性劑加上乙醇的存在而具有起 始防霧性。短時間後失去防霧性而後再恢復。其理由如 下。光催化劑之光激反應不僅分解乙醇,同時也分解界 面活性劑’得到一個中間產物,在分解過程中,失去親 水性’結果暫時性地失去防霧性。然而,在界面活性劑 完全分解後’又恢復其親水性,而重建防霧性。 .經濟部中央標準局員工消費合作社印製 此結果證明光催化氧化鈦顆粒,矽土,和乙醇之外 ’再添加界面活性劑,不僅得到永久的防霧性,也同時 得到起始防霧性。 界面活性劑用量越大,暫時失去防霧性的時間越長 。特別地’塗層液體樣品Β2塗層之樣品,其界面活性劑 添加量小至0.4份重量比,相較於一份重量比光催化氧化 鈦顆粒,失去的時間約為2小時,而塗層液體樣品Β3塗層 本紙張尺度適用中國國家標準(CNS ) Α4規格(21〇χ 297公釐) ~》一 ^67943 A7 B7 五、發明説明(31 ) 之樣品,其界面活性劑添加量為1份重量比,相較於一份 重比光催化氧化欽顆粒,失去的時間約為5小時,而塗 層液體樣品B4塗層之樣品,其界面活性劑添加量為2份重 量比,相較於一份重量比光催化氧化鈦顆粒,失去的時 間約為24小時。另外,塗層液體塗層之樣品,其界面活 性劑添加置為1 〇份重置比,相較於一份重量比光催化氧 化鈦顆粒者’其失去的時間約為200小時或更長。 當塗層液體為氣霧劑型時,防霧性暫時失去的時間 較佳的是1天或少於1天’界面活性劑添加量較佳的是少 於10份重量比,更佳的是不超過2份重量比. 另外,以BLB光線照射50小時之基質玻璃和塗層液體 樣品B1至B4塗層於玻璃表面之樣品,測量其樣品表面與 水的接觸角。以接觸角角度測向計(CA_X15〇,Ky〇wa Interface Science Co. ,Ltd.製造),以微注射器滴一水 滴至樣品表面’ 30秒後測1樣品表面與水的接觸角。 經濟部中央榡準局員工消費合作社印製 結果,基質玻璃接觸角為30。’而所有塗層液體樣品 B1至B4塗層製備之基質玻璃表面樣品,均有良好的血水 的接觸角,.也就是說,接觸角約為 另外,塗層液體樣品B1至B4塗層製備之基質玻璃表 面樣品,該等樣品均測過與水之接觸角,評估去除油污 的可能性。特別地,以油酸層塗於各樣品表面,然後將 各樣品浸入水槽中的水,而使樣品表面水平放置。 結果,油酸變為圓球狀,而輕輕摩擦使得油滴由樣 品表面釋放出來。. 本紙張適用巾國國家標準(CNS ) A4規格.(2Ι〇χ297公廣) --—- ™ 34 — 467943 經濟部t央標準局員工消費合作社印製 A7 B7 五、發明説明(.32 ) 實例B2 添加陰離子或非離子界面活性劑對光澤产之影 響 又w 氧化鈦溶耀"(ST-KOI)和氧化鈦溶膠(ST~K〇3)(固體含 里10/έ重1比’ >容質為5份重量比之氧化敛(銳欽礦)和5份 重量比之燒基梦土)以1 : 1混合,該混合物以丙醇稀釋 倍’製備光催化塗層樣品Β5。樣品Β5加入山梨糖醇野單 辛酸酯(一個非離子界面活性劑)〇. 05%重量比(相當於 0.325%重量比氧化鈦),製備樣品Β6。樣品Β5加入山梨糖 醇酐單辛酸酯〇_ 1%重量比(相當於0. 65%重量比氧化鈦), 製備樣品Β7。樣品Β5加入一個四級銨鹽(陰離子界面活性 劑)〇_〇5%重量比,製備樣品Β8。另外,樣品邯加入一個 四級銨鹽0.1%重量比,製備樣品Β9。 樣品Β5至Β9 ’以澆流塗層法層塗於以乙醇擦拭之深 灰色層塗鋼板’處理過之鋼板於室溫靜置18小時(約2〇。) 。此樣品,依照日本工業標準(JIS)Z8741設定之方法, 測量其光澤度。結果’層塗鋼板之光澤度為94。另外, 樣品B5之光澤度為96,而添加界面活性劑之樣品別至B9 之光澤度分別為102 ’ 110,106,和112,此結果顯示, 添加界面活性劑會造成光澤度。 然後’樣品B5至B9以澆流塗層法層塗於以乙醇擦拭 之載玻片’而層塗的載玻片靜置於室溫(約2〇。)18小時。 而後,這些樣品以紫外光照射強度為〇·5 rnW/cm2之光源 (black light blue (B3LB 螢光燈),Sankyo Denki 製造)光 線照射’以測定塗層防霧性對照以光線照射時間為函數 本紙張尺度適用中國國家標率(CNS ) A4規格(210 X 297公策) (請先閎讀背面之注意事^寫本頁)467943 A7 Printed B7 by the Consumers' Cooperatives of the Ministry of Economic Affairs, China Standards Bureau, V. Invention Description (.28) 〇 Example A4 Adding surfactant titanium oxide solution (TA-15) and wonderful soil solution " (" Glasca A ") is mixed, and the mixture is diluted with ethanol to prepare a coating liquid, in which the concentration of titanium oxide particles is 0.5% by weight and the concentration of silica particles is 0.5% by weight. Evening soil sol (M Glasca AM) and surfactant polyethylene glycol (molecular weight 3000) were mixed, and the mixture was diluted with ethanol to prepare a coating liquid, in which the concentration of titanium oxide particles was 0.5% by weight and the concentration of silica particles It is 0.5% by weight, and the polyethylene glycol concentration is 0.2% by weight. Titanium oxide sol (TA-15) is mixed with silica sol (" Glasca A ") and modified polysilica (KF-351, Polyzaki type, manufactured by The Shin-Etsu Chemical Co., Ltd.), and the mixture is 2 重量 比 , Diluted with ethanol to prepare a coating liquid, wherein the concentration of titanium oxide particles is (] .5% by weight, the concentration of silica particles is 0.5% by weight, and the concentration of modified polylith is 0.2% by weight In addition, a titanium oxide sol (TA-15) is mixed with a silica sol (" Glasca A ") and a modified polysilica (KF-945 'polyether type, manufactured by The Shin-Etsu Chemical Co., Ltd.) The mixture was diluted with ethanol to prepare a coating liquid having a titanium oxide particle concentration of 0.5% by weight, a silica particle concentration of 0.5% by weight, and a modified polysilicon concentration of 0.2 by weight. Coated to 10 square centimeters of soda-lime glass substrate, the layer-coated substrate was placed at 50. (: one hour, and then left to stand for 15 minutes to cool the layer-coated substrate to obtain samples A6 to A9. (Please read the precautions on the back first) (4 write this page)-Binding-Binding · Thread paper size is applicable to China National Standard (CNS) A4 specification (2ί〇Χ297 mm) ) -31-4 6 7 9 4 3 A7 B7 V. Description of the invention (29) Samples A6 to A⑽ UV light source (BLB fluorescent lamp) of 25 mW / Gm2 are irradiated to determine the anti-fogging property of the coating And the change graph as a function of light irradiation time. The results are shown in Fig. 6. In particular, sample A6 has good anti-fogging properties after being irradiated for 2 hours (◎) 3 In addition, sample A7 has good anti-fogging irradiation times. (◎) It is 3 hours, sample A8 is 4 hours, and sample A9 is not less than 20 hours. The results show that with the addition of surfactants, the effect of hydrophobicity is longer. Mist. Additive amount of surfactant titanium oxide sol (TA-15), silica sol (" Glasca a "), polyoxyethylene p-alkyl phenyl ether (Penerole, NP-95, manufactured by Matsumoto Yushi ) And non-ionic surfactant, mixed with ethanol to prepare coating liquid samples B1 to B4, these samples contain titanium oxide particles, silica particles, and surfactant are dispersed in the solvent, (Please read the note on the back first Write this page; >-equipment _-in the Ministry of Economic Affairs Samples printed by the staff of the Bureau of Standards and Consumers Cooperative Co., Ltd. Titanium oxide (benefit ratio) Relative soil particles (part-to-amount ratio) and active agent (part-by-weight ratio) Β1 50 25 0 Β2 50 25 20 Β3 50 25 so Β4 50 25 1 〇〇 Coating liquid samples B1 to B4 were applied to the soda-lime glass substrate, and the coating was dried and then irradiated with a UV light source (black light blue (BLB fluorescent lamp), manufactured by Sankyo Denki) with an intensity of 0.25 mW / cm2. Light exposure 'to determine the anti-fogging properties of the coating and a graph of change as a function of light exposure time. The results are shown in Fig. 7 ^ In addition, the anti-fogging property was evaluated using the evaluation criteria of Example A1. This paper size is applicable to China Standard (CNS) A4 (2mx297 cm) wire. • frr II * / 94 3 Α7 87 V. Description of the invention (30) As shown in Figure 7, no matter how long the ultraviolet light is irradiated The matrix glass basically only exhibits anti-fogging grade X. However, after 50 hours of UV light irradiation, the samples of all coating liquid samples B1 to B4 have good anti-fogging properties on the surface of the matrix glass (◎ ). The coating liquid samples B1 did not exhibit anti-fogging properties before UV light irradiation, and the coating liquid samples B2 to B4 showed anti-fogging properties before and after UV light irradiation. Coating liquid sample B1 The reason that the coating sample does not have initial anti-fogging property is considered to be that ethanol remains in the coating. Increasing the irradiation time to obtain anti-fogging 'may be due to the photo-excited reaction of the photocatalyst to decompose ethanol. In contrast, the samples prepared from the coating liquid samples B2 to B4 doped with a surfactant have antifogging properties due to the presence of the surfactant plus ethanol. After a short time, it loses its anti-fog property and then recovers. The reason is as follows. The photo-excited reaction of the photocatalyst not only decomposes ethanol, but also decomposes the surfactant 'to obtain an intermediate product. During the decomposition process, the hydrophilicity is lost' and the antifog property is temporarily lost. However, after the surfactant is completely decomposed ', it returns to its hydrophilicity, and the antifogging property is restored. Printed by the Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs This result proves that the addition of surfactants in addition to photocatalytic titanium oxide particles, silica, and ethanol will not only obtain permanent antifog, but also get initial antifog . The larger the amount of surfactant, the longer it will temporarily lose the anti-fog property. In particular, the coating liquid sample B2 coating sample has a surfactant addition amount as small as 0.4 parts by weight, compared to one part by weight photocatalytic titanium oxide particles, the time lost is about 2 hours, and the coating Liquid sample B3 coating The paper size is in accordance with Chinese National Standard (CNS) A4 specification (21〇χ 297 mm) ~ "^ 67943 A7 B7 V. Sample of invention description (31), the surfactant addition amount is 1 Part by weight ratio, compared to one part by weight photocatalytic oxidation of Chin particles, the time lost is about 5 hours, while the coating liquid sample B4 coating sample, the surfactant addition amount is 2 parts by weight, compared to At a weight ratio of photocatalytic titanium oxide particles, the loss time is about 24 hours. In addition, the sample of the coating liquid coating had the surfactant added at a reset ratio of 10 parts, and the lost time was about 200 hours or more compared to one part by weight of the photocatalytic titanium oxide particles. When the coating liquid is an aerosol formulation, the time for which the antifogging property is temporarily lost is preferably 1 day or less. The added amount of the surfactant is preferably less than 10 parts by weight, and more preferably More than 2 parts by weight. In addition, the substrate glass and coating liquid samples B1 to B4 irradiated with BLB light for 50 hours were measured on the glass surface, and the contact angle between the sample surface and water was measured. Using a contact angle angle goniometer (CA_X150, manufactured by Kyowa Interface Science Co., Ltd.), a piece of water was dripped onto the sample surface with a microsyringe, and the contact angle of the sample surface with water was measured after 30 seconds. Printed by the Consumers' Cooperative of the Central Government Bureau of the Ministry of Economic Affairs, the contact angle of the matrix glass was 30. 'And all coating liquid samples B1 to B4 coated substrate glass samples have good contact angle of blood and water, that is, the contact angle is about the same, coating liquid samples B1 to B4 coating prepared Samples on the surface of the matrix glass. These samples have been tested for contact angle with water to evaluate the possibility of removing oil. Specifically, the surface of each sample was coated with an oleic acid layer, and then each sample was immersed in water in a water tank, so that the surface of the sample was placed horizontally. As a result, oleic acid becomes spherical, and light rubbing causes oil droplets to be released from the surface of the sample. . This paper applies the national standard (CNS) A4 standard of towels. (2Ι〇χ297 public broadcasting) ------- ™ 34 — 467943 Printed by the Consumers Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (.32) Example B2 The effect of adding anionic or non-ionic surfactants on gloss production and titanium oxide dissolve " (ST-KOI) and titanium oxide sol (ST ~ K〇3) (solid content 10 / weight 1 ratio ' > The content is 5 parts by weight of oxidized condensate (Rhiqin ore) and 5 parts by weight of calcined montmorillonite) were mixed at 1: 1, and the mixture was diluted with propanol to prepare a photocatalytic coating sample B5. Sample B5 was prepared by adding sorbitol wild monocaprylate (a nonionic surfactant) at 0.05% by weight (equivalent to 0.325% by weight titanium oxide). Sample B5 was added with sorbitan monocaprylate 0-1% by weight (equivalent to 0.65% by weight titanium oxide) to prepare sample B7. Sample B5 was prepared by adding a quaternary ammonium salt (anionic surfactant) in an amount of 0.05% by weight to prepare sample B8. In addition, a sample quaternary ammonium salt was added at 0.1% by weight to prepare sample B9. Samples B5 to B9 were coated with a dark gray layer coated steel plate wiped with ethanol by a flow coating method, and the steel plate treated was left at room temperature for 18 hours (about 20 °). The gloss of this sample was measured in accordance with the method set by the Japanese Industrial Standard (JIS) Z8741. As a result, the gloss of the 'layer-coated steel sheet was 94. In addition, the gloss of sample B5 is 96, and the gloss of samples added with surfactants to B9 is 102 ′ 110, 106, and 112, respectively. This result shows that the addition of surfactants will cause gloss. Then, "samples B5 to B9 were layer-coated on a glass slide wiped with ethanol by a flow coating method", and the layer-coated glass slide was left to stand at room temperature (about 20 ° C) for 18 hours. These samples were then irradiated with a light source (black light blue (B3LB fluorescent lamp), manufactured by Sankyo Denki) with a UV light intensity of 0.5 rnW / cm2 to determine the antifogging properties of the coating. The control was based on the light exposure time as a function. This paper size is applicable to China National Standards (CNS) A4 specifications (210 X 297 public policy) (Please read the notes on the back first ^ write this page)

467943 經濟部中央標準局員工消費合作社印製 A7 B7五、發明説明(33 ) 的變化。結果,發現樣品B5至B7從開始就具有良好的防 霧性(◎),樣品B8,以紫外光照射1.5小時後,具有良好 的防霧性◎,而樣品B9以紫外光照射5小時後,具有良好 的防霧性(§)。 實例C1 添加陽離子界面活性劑 水(2450份重量比)和0. 025份重量比陽離子界面活性 劑(Rapisol A-80,Nippon Oils & Fats Co. ,Ltd.製造) 加至氧化鈦溶膠(ST-K01),製備得樣品Cl。 水(2450份重量比)和0. 25份重量比陽離子界面活性 劑(Rapisol A-80,Nippon Oils & Fats Co. ,Ltd.製造) 加至氧化鈦溶膠(ST-K01)製備得樣品C2。 樣品Cl和C2靜置3天,此時間内未發生凝結現象。隨 後,樣品C1和C2以澆流塗層法層塗於10平方公分之鈉鈣 玻璃片,塗層於室溫乾燥一小時製備得樣品C3和C4。 樣品C3和C4,未有霧狀產生也沒有看到干擾邊緣, 而形成一個透明,均勻的塗層。 然後,樣品C3和C4之表面這些樣品以紫外光照射強 度為 0.25 mW/cm2之光源(black light blue (BLB 螢光燈) ,Sankyo Denki製造)光線照射一天,然後測試這些樣品 與水的接觸角,防霧性,和以水除去油污的情形。以接 觸角角度測向計(CA-X150,Kyowa Interface Science Co. ,:Ltd.製造),以微注射器滴一水滴至樣品表面,30秒後 測量樣品表面與水的接觸角。 結果,樣品C3和C4二者都高度親水化,其與水的接 (請先閱讀背面之注意事項寫本頁) -裝- 線_ 本紙張尺度適用中囷國家標準(CNS ) A4規格(2! 0 X 297公釐) -36 - 4 94 3 A7 B7 經濟部中夬榡準局員工消費合作社印製 五、發明説明(34 ) 觸角約為〇。。相對的,接觸角鈉玻璃片與水的接觸角約 為 30。。 以實例A1所採用相同的評定標準評估其防霧性。 結果,樣品C3和C4二者均有良好的防霧性(◎) β 另外,樣品C3和C4也進行油污去除可能性之評估。 /由酸層塗於各樣品表面,各樣品浸入水槽中的水,而使 樣品表面水平放置。 結果,油酸變為圓球狀,而輕輕摩擦使得油滴由樣 品表面釋放出來。 小物件添加醇類 氡化鈦溶膠(ST-K01)以2-丙醇稀釋25倍,得到塗層 液體樣品D1。 孩塗層液體以喷霧層塗於一個1〇平方公分鈉鈣玻璃 基質,塗層於室溫(20。〇乾燥20分鐘,使塗層硬化,製備 得樣品D2。 、、另外,氧化鈦溶膠(ST〜K01)以乙醇稀釋25倍,得到 塗層液體樣品D3。 塗層液體以m層法層塗於—個1G平方公分納雨 ^璃基質,塗層於室溫(啊)乾制分鐘,使塗層硬化, I備得樣品D4。 接著,檢測樣品D2和D4|%水的接觸角和其外觀。 /品D2和D4的表面以料歧㈣度被5禮—2之 :原(black light blue (BLB 榮光燈),Sanky〇 Denki 製 以)光線照射24小時。照射後,測量該等樣品與水的接觸 本紙張妓適用中CNS) A4· ( (請先閲讀背面之注意事項¾寫本頁) .裝. 0 ,^ιτ 線 -37 - 4 6 7^43467943 Printed by the Consumers' Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs A7 B7 V. Changes in Invention Description (33). As a result, it was found that samples B5 to B7 had good anti-fogging properties from the beginning (◎), and sample B8 had good anti-fog properties after being irradiated with ultraviolet light for 1.5 hours ◎, while sample B9 was irradiated with ultraviolet light for 5 hours, Has good anti-fog properties (§). Example C1 A cationic surfactant water (2450 parts by weight) and 0.025 parts by weight of a cationic surfactant (Rapisol A-80, manufactured by Nippon Oils & Fats Co., Ltd.) were added to a titanium oxide sol (ST -K01) to prepare a sample Cl. Water (2450 parts by weight) and 0.25 parts by weight of a cationic surfactant (Rapisol A-80, manufactured by Nippon Oils & Fats Co., Ltd.) were added to a titanium oxide sol (ST-K01) to prepare a sample C2 . Samples Cl and C2 were left standing for 3 days, and no coagulation occurred during this time. Subsequently, samples C1 and C2 were coated on a soda-lime glass sheet of 10 square centimeters by a flow coating method, and the coatings were dried at room temperature for one hour to prepare samples C3 and C4. Samples C3 and C4 showed no haze and no disturbing edges, but formed a transparent, uniform coating. Then, the surfaces of the samples C3 and C4 were irradiated with a light source (black light blue (BLB fluorescent lamp), manufactured by Sankyo Denki) with an intensity of 0.25 mW / cm2 under ultraviolet light for one day, and then the contact angle of these samples with water was measured. , Anti-fogging, and the case of removing oil with water. Using a contact angle angle goniometer (CA-X150, manufactured by Kyowa Interface Science Co.,: Ltd.), a drop of water was dropped on the sample surface with a micro syringe, and the contact angle of the sample surface with water was measured after 30 seconds. As a result, both samples C3 and C4 are highly hydrophilized, and their connection with water (please read the precautions on the back to write this page first) -Installation-Thread_ This paper size applies to the China National Standard (CNS) A4 specification (2 ! 0 X 297 mm) -36-4 94 3 A7 B7 Printed by the Consumers' Cooperative of the China Standards and Quarantine Bureau of the Ministry of Economic Affairs. 5. Description of the invention (34) The antenna angle is about 0. . In contrast, the contact angle of the soda glass plate with water is about 30. . The anti-fog property was evaluated using the same evaluation standard as that used in Example A1. As a result, both samples C3 and C4 had good anti-fogging properties (◎) β In addition, samples C3 and C4 were also evaluated for the possibility of oil removal. / The surface of each sample is coated with an acid layer, and each sample is immersed in water in a water tank, so that the surface of the sample is placed horizontally. As a result, oleic acid becomes spherical, and light rubbing causes oil droplets to be released from the surface of the sample. Alcohols were added to small objects. Titanium trioxide sol (ST-K01) was diluted 25-fold with 2-propanol to obtain coating liquid sample D1. The coating liquid was spray-coated on a 10 cm² soda-lime glass substrate, and the coating was dried at room temperature (20 ° C for 20 minutes to harden the coating to prepare sample D2. In addition, a titanium oxide sol was prepared. (ST ~ K01) Diluted 25 times with ethanol to obtain coating liquid sample D3. The coating liquid was coated on a 1G cm 2 nano-glass substrate with m layer method, and the coating was dried at room temperature (ah) for one minute. To harden the coating, I prepared sample D4. Next, check the contact angles and appearances of samples D2 and D4 |% water. The surface of product D2 and D4 was judged by the material disparity 5-2: original ( black light blue (BLB glory lamp), made by Sanky〇Denki) light irradiation for 24 hours. After exposure, measure the contact of these samples with water CNS for paper prostitutes A4 · ((Please read the precautions on the back first ¾ (Write this page). Outfit. 0, ^ ιτ 线 -37-4 6 7 ^ 43

五、發明説明(35 ) 經濟部中央樣準局員工消費合作社印製 以接觸角角度測向計(CA—xi5〇,Kyowa Interface Science Co.,Ltd♦製造),以微注射器滴一水滴至樣品 表面’ 30秒後測量樣品表面與水的接觸角。 結果,樣品D2和D4二者都高度親水化,其與水的接 觸角約為0。。另外,樣品])2和D4之塗層外觀透明而且沒有 失去其均句性》 大物件添加醇類 實例D1之塗層液體樣品Di以澆流塗層法層塗於一個 50平方公分之鈉鈣玻璃基質,塗層於室溫(2〇。〇乾燥2〇分 鐘,使塗層硬化,製備得樣品D5。 另外’塗層液體樣品D3以澆流塗層法層塗於一個5〇 平方公分之鈉鈣玻璃基質,塗層於室溫(2〇。〇乾燥20分鐘 ,使塗層硬化,製備得樣品D6. 樣品D5和D6檢測該等樣品與水的接觸角和其外觀。 樣品D5和D6的表面以紫外光照射強度為〇. 5 mff/cm2之 光源(black light blue (BLB 榮光燈),Sankyo Denki 製 造)光線照射24小時。照射後,測量該等樣品與水的接觸 角’以接觸角角度測向計(CA-X150,Kyowa Interface Science Co.,Ltd.製造),以微注射器滴一水滴至樣品 表面,30秒後測量樣品表面與水的接觸角。 結果,樣品D5和D6二者都高度親水化,其與水的接 觸角約為0°。 然而,在這種情形下,樣品D6,很明顯的在遑流塗 層起始點有混濁現象,而樣品D5,塗層外觀透明而且沒 本紙張尺度適用中國國家標準(CNS ) A4洗格(210X297公釐) —---'r—-----裝-- (請先閣讀背面之注意事項^'4寫本頁) 訂 -3S - 4 6 7 9 4 3 經濟部中央標隼局員工消費合作社印製 A7 B7 五、發明説明(36 ) 有失去其均勻性。 由此結果得知,在大物件使用丙醇是較佳的。 實例D3 大物件添加醇類 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(ST-K03)以1 : 1比 例混合,該混合物以2-丙醇稀釋25倍,製備得塗層液體 樣品D7。 塗層液體樣品D7以澆流塗層法層塗於一個50平方公 分之鈉鈣玻璃基質,塗層於室溫(20°C)乾燥20分鐘,使塗 層硬化,製備得樣品D8。 接著,樣品D8以實例D1相同的方法檢測該樣品與水 的接觸角和外觀。 結果,發現樣品D8超高度親水化,其與水的接觸角 約為0°,而塗層外觀透明而且沒有失去其均勻性。 實例D4 大物件添加醇類 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(STHE(03)以1 : 1比 例混合,該混合物以8 : 2之2-丙醇和丙二醇單丙基醚混 合物稀釋25倍,製備得塗層液體樣品D9。 塗層液體樣品D9以澆流塗層法層塗於一個50平方公 分之鈉鈣玻璃基質,塗層於室溫(20°C)乾燥20分鐘,使塗 .層硬化,製備得樣品D10。 接著,樣品D10以實例D1相同的方法檢測該樣品與水 的接觸角和外觀。 結果,發現樣品D10超高度親水化,其與水的接觸角 約為0°,而塗層外觀透明而且沒有失去其均勻性。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閲讀背面之注意事項厂1¾寫本頁) -裝. 訂 -39 - 467943 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明(37 ) 實例的大物件添加醇類 氧化钦容膠(灯-KOl)和氧化鈦溶膠(ST-K03)以1 : 1比 例昆合’該混合物以9 : 1之2_丙醇和二两酮醇(4_羥基_4_ 甲基戊嗣)混合物稀釋25倍,製備得塗層液體樣品Dn(pH 4) ° 塗層液體樣品Dll以洗流塗層法層塗於一個5〇平方公 分之納#5玻璃基質’塗層於室溫.(2〇dc)乾燥2〇分鐘,使塗 層硬化’製備得樣品D12。 接著’樣品D12以實例D1相同的方法檢測該樣品與水 的接觸角和外觀。+ .結果’發現樣品D12超高度親水化,其與水的接觸角 約為0° ’而塗層外觀透明而且沒有失去其均勻性。 實盤P!應用至汽車體:添加均質劑 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(ST-K03)以1 : 1比 例混合’該混合物以9 : 1之2-丙醇和二丙酮醇混合物稀 釋25倍’製備得塗層液體樣品D13。 塗層液體樣品D13以澆流塗層法層塗於汽車車蓋(引 擎頂蓋)上,塗層於室溫(20。〇乾燥20分鐘,使塗層硬化 ’製備得樣品D14。 樣品D14以實例D1相同的方法檢測該樣品與水的接觸 角和外觀。 結果,發現樣品D14超高度親水化,其與水的接觸角 約為0°。塗層表面是平滑的,而塗層外觀透明而且沒有 失去其均句性。 本紙張尺度適用t國國家檩牟(CNS ) A4規格(210 X 297公釐) (請先閱讀背面之注意事策彳填寫本頁) -裝- 訂 線 -40 - A7 經濟部中央標準局員工消費合作社印製 __B7_五、發明説明( 3S) . 實例D7 應用至汽車體:添加均質劑 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(ST-K03)以1 : 1比 例混合,該混合物以8 : 1 : 1乙醇,2-丙醇,和二丙酮醇 混合物稀釋25倍,製備得塗層液體樣品D16。 塗層液體樣品D15以澆流塗層法層塗於汽車車蓋(引 擎頂蓋)上,塗層於室溫(20°C)乾燥20分鐘,使塗層硬化 ,製備得樣品D16。 樣品D16以實例D1相同的方法檢測該樣品與水的接觸 角和外觀。 結果,發現樣品D16超高度親水化,其與水的接觸角 約為0°。塗層表面是平滑的,而塗層外觀透明而且沒有 失去其均勾性。 實例D8 添加乙醇與均質劑 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(ST-K03)以1 : 1比 例混合,該混合物以8 : 2之2-丙醇和丙二醇單丙基醚混 合物稀釋25倍,製備得塗層液體樣品D17。 塗層液體樣品D17以澆流塗層法層塗於一個50平方公 分之鈉鈣玻璃基質,塗層於室溫(20°C)乾燥20分鐘,使塗 層硬化,製備得樣品D18。 ' 接著,樣品D18以實例D1相同的方法檢測該樣品與水 的接觸角和外觀。 結果,發現樣品D18超高度親水化,其與水的接觸角 約為0°,而塗層外觀透明而且沒有失去其均勻性。 實例D9 添加乙醇與均質劑 (請先閱讀背面之注意事項Γ4寫本頁) -裝. 訂 線 本紙浪尺度適用中國國家標準(CNS ) Μ規格(2SOX297公釐) -41 - 6 4 經濟部中央標準局員工济費合作社印製 7 9 4 3 A7 〜—_____ 五、發明説明(39 ) 氧化鈦溶膠(ST-K01)和氧化鈦溶膠(ST-K03)以1 : 1比 例混合,該混合物以9 : 1乙醇和丁基溶纖素(2-丁氧基乙 醇)混合物稀释25倍,製備得塗層液體樣品D19。 塗層液體樣品D19以澆流塗層法層塗於汽車車蓋(引 1 擎頂蓋)上,塗層於室溫(20。〇乾燥20分鐘,使塗層硬化 ’製備得樣品D20。 接著,樣品D20以實例D1相同的方法檢測該樣品與水 的接觸角和外觀。 結果,發現樣品D20超高度親水化,其與水的接觸角 約為0。’而塗層外觀透明而且沒有失去其均勻性。 iMDIO氣霧劑組合物 實例D5製備之塗層液體樣品D11和氮氣以6 : 4體積比 填充於圖1氣溶膠容器内。塗層液體樣品Dll由此氣霧劑 容器喷霧至一個載玻片基質,該塗層於室溫靜置30分鐘 ’製備得樣品D13。 樣品D13以實例D1相同的方法檢測該樣品與水的接觸 角和外觀。 結果’發現樣品D13超高度親水化,其與水的接觸角 約為0。’而塗層外觀透明而且沒有失去其均勻性。 塗層固體含量和透明度 鈉鈣玻璃板(40 XI〇〇 X 2mm)浸入以乙醇稀釋之氧化鈦 溶膠(ST-K01)溶液,以24 cm/min之拉提速度將鈉鈣玻璃 拉上而完成浸潰層塗。氧化鈦溶膠以乙醇稀釋至下面的 固體含量==然後,塗層於5〇χ或15〇τ加熱,製備得樣品 本纸張纽ϋ财關家標準(CNS「Α4規格(21GX_297公楚) .(請先聞讀背面之注意事項.rl^-寫本頁) ------------裝--;----- 訂 -42 - 4 6 7 94 3 Α7 Β7 五、發明説明(40 ) 至E8。以濁度計(Hazegardplus,Gardener製造)測量這些 樣品之?昆ί蜀狀況。 結果簡要說明於下表。 品 樣 12 3 4 5 6 Ε Ε Ε Ε Ε Ε Ε Ε 固體含量 (wt%) 10 5 10.1 10 5 1 0.1 熱處理溫 度(。〇 50 50 50 50 150 150 150 150V. Description of the invention (35) Printed with a contact angle angle goniometer (CA-xi50, manufactured by Kyowa Interface Science Co., Ltd.) at the Consumer Cooperatives of the Central Procurement Bureau of the Ministry of Economic Affairs, a drop of water was dripped onto the sample with a microsyringe Surface 'After 30 seconds, the contact angle of the sample surface with water was measured. As a result, both samples D2 and D4 were highly hydrophilic, and their contact angle with water was about 0. . In addition, the samples]) 2 and D4 are transparent in appearance and have not lost their homogeneity. ”Large objects are added with the coating liquid sample D1 of the alcohol example D1. Glass substrate, the coating was dried at room temperature (20.0 minutes for 20 minutes, and the coating was hardened to prepare sample D5. In addition, the coating liquid sample D3 was applied by a flow coating method to a layer of 50 cm 2 Soda-lime glass substrate, the coating was dried at room temperature (20 ° C for 20 minutes, the coating was hardened, and sample D6 was prepared. Samples D5 and D6 were tested for the contact angle and appearance of these samples with water. Samples D5 and D6 The surface was irradiated with ultraviolet light (black light blue (BLB glory lamp), manufactured by Sankyo Denki) with an intensity of 0.5 mff / cm2 for 24 hours. After the irradiation, the contact angle of the samples with water was measured to make contact An angle goniometer (CA-X150, manufactured by Kyowa Interface Science Co., Ltd.), a drop of water was dropped on the sample surface with a micro syringe, and the contact angle between the sample surface and water was measured after 30 seconds. As a result, samples D5 and D6 were Are highly hydrophilic, and their contact with water The angle is about 0 °. However, in this case, sample D6 clearly has turbidity at the starting point of the flow coating, while sample D5, the coating has a transparent appearance and does not conform to the Chinese national standard for this paper size ( CNS) A4 wash case (210X297mm) ----- 'r ------- install-(please read the precautions on the back first ^' 4 write this page) Order -3S-4 6 7 9 4 3 Printed by A7 B7, Consumer Cooperatives of the Central Bureau of Standards, Ministry of Economic Affairs 5. Description of the invention (36) It has lost its uniformity. From this result, it is learned that propanol is better for large objects. Example D3 Add alcohol to large objects A titanium oxide sol (ST-K01) and a titanium oxide sol (ST-K03) were mixed at a ratio of 1: 1, and the mixture was diluted 25-fold with 2-propanol to prepare a coating liquid sample D7. The coating liquid sample D7 was The flow-coating method was applied to a 50-cm² soda-lime glass substrate, and the coating was dried at room temperature (20 ° C) for 20 minutes to harden the coating to prepare sample D8. Next, sample D8 was the same as Example D1. The contact angle and appearance of the sample with water were detected by the method. As a result, it was found that the sample D8 was extremely highly hydrophilized and its contact angle with water It is about 0 °, and the coating has a transparent appearance without losing its uniformity. Example D4 A large object is added with an alcohol-based titanium oxide sol (ST-K01) and a titanium oxide sol (STHE (03) in a 1: 1 ratio, and the mixture is A coating liquid sample D9 was prepared by diluting a 25-fold mixture of 2-propanol and propylene glycol monopropyl ether in 8: 2. The coating liquid sample D9 was applied to a 50 cm 2 sodium lime glass substrate by a flow coating method. The coating was dried at room temperature (20 ° C) for 20 minutes to harden the coating to prepare sample D10. Next, sample D10 was tested for the contact angle and appearance of the sample with water in the same manner as in Example D1. As a result, it was found that the sample D10 was extremely highly hydrophilized, and its contact angle with water was about 0 °, and the appearance of the coating was transparent without losing its uniformity. This paper size applies to China National Standard (CNS) A4 (210X297 mm) (Please read the precautions on the back of the factory 1¾ to write this page)-Packing. Order -39-467943 A7 B7 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs Preparation of the fifth, description of the invention (37) Example of a large object added alcohol oxidized acrylic glue (lamp-KOl) and titanium oxide sol (ST-K03) in a ratio of 1: 1: the mixture is 9: 1 to 2_ A mixture of propanol and di-diketol (4_hydroxy_4_methylpentamidine) was diluted 25 times to prepare a coating liquid sample Dn (pH 4) ° The coating liquid sample Dll was applied to a 5 layer by a wash-flow coating method. Nanometer # 5 glass substrate 'coating was dried at room temperature. (20 dc) for 20 minutes, and the coating was hardened to prepare sample D12. Next, 'Sample D12' was used to examine the contact angle and appearance of the sample with water in the same manner as in Example D1. +. As a result, it was found that the sample D12 was extremely highly hydrophilized, its contact angle with water was about 0 °, and the coating had a transparent appearance without losing its uniformity. Hard disk P! Application to the car body: Add homogenizers titanium oxide sol (ST-K01) and titanium oxide sol (ST-K03) mixed in a 1: 1 ratio 'The mixture is 2-propanol and diacetone alcohol 9: 1 The mixture was diluted 25 times to prepare a coating liquid sample D13. Coating liquid sample D13 was applied on the car cover (engine hood) by the flow coating method, and the coating was dried at room temperature (20 ° C for 20 minutes to harden the coating). Sample D14 was prepared. The contact angle and appearance of the sample with water were measured in the same manner as in Example D1. As a result, it was found that the sample D14 was ultra-hydrophilic, and its contact angle with water was about 0 °. The coating surface was smooth, and the appearance of the coating was transparent and It does not lose its uniformity. This paper size is applicable to the national standard (CNS) A4 (210 X 297 mm) of the country (Please read the precautions on the back first and fill in this page)-Binding-Thread -40- A7 Printed by the Consumer Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs__B7_ V. Description of Invention (3S). Example D7 is applied to automobile bodies: adding homogenizers titanium oxide sol (ST-K01) and titanium oxide sol (ST-K03) to The mixture was mixed in a ratio of 1: 1, and the mixture was diluted 25 times with a mixture of 8: 1: 1 ethanol, 2-propanol, and diacetone alcohol to prepare a coating liquid sample D16. The coating liquid sample D15 was deposited by a flow-coating method Apply on the car cover (engine hood), the coating is dried at room temperature (20 ° C) Dry for 20 minutes to harden the coating to prepare sample D16. Sample D16 was tested for the contact angle and appearance of the sample with water in the same manner as in Example D1. As a result, it was found that sample D16 was extremely highly hydrophilized, and its contact angle with water was about 0 °. The surface of the coating is smooth, while the appearance of the coating is transparent without losing its uniformity. Example D8 Adding ethanol and homogenizer titanium oxide sol (ST-K01) and titanium oxide sol (ST-K03) to 1 : 1 ratio mixing, the mixture was diluted 25 times with 8: 2 of 2-propanol and propylene glycol monopropyl ether mixture to prepare a coating liquid sample D17. The coating liquid sample D17 was applied to a 50 layer by a flow coating method. Sodium lime glass substrate, the coating was dried at room temperature (20 ° C) for 20 minutes, and the coating was hardened to prepare sample D18. 'Next, sample D18 was tested for water contact with the sample in the same manner as in Example D1. Angle and appearance. As a result, it was found that sample D18 was extremely highly hydrophilized, its contact angle with water was about 0 °, and the coating was transparent without losing its uniformity. Example D9 Adding ethanol and homogenizer (please read the back Note Γ4 write (Page)-Binding. The size of the paper is set to the Chinese National Standard (CNS) M specification (2SOX297 mm) -41-6 4 Printed by the Employees' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 7 9 4 3 A7 ~ —_____ V. Description of the invention (39) Titanium oxide sol (ST-K01) and titanium oxide sol (ST-K03) are mixed at a ratio of 1: 1, and the mixture is diluted with a 9: 1 ethanol and butylcellosolve (2-butoxyethanol) mixture 25 times, a coating liquid sample D19 was prepared. The coating liquid sample D19 was applied on the car cover (injection 1) by the flow coating method, and the coating was dried at room temperature (20 ° C for 20 minutes to harden the coating) to prepare sample D20. The sample D20 was tested in the same manner as in Example D1 for the contact angle and appearance of the sample with water. As a result, it was found that the sample D20 was ultra-hydrophilic, and its contact angle with water was about 0. 'And the appearance of the coating was transparent without losing Uniformity. A coating liquid sample D11 and nitrogen prepared by iMDIO aerosol composition example D5 were filled in the aerosol container of FIG. 1 at a volume ratio of 6: 4. The coating liquid sample D11 was sprayed from this aerosol container to one. Slide glass substrate, the coating was left to stand at room temperature for 30 minutes to prepare sample D13. Sample D13 was tested for the contact angle and appearance of the sample with water in the same manner as in Example D1. As a result, it was found that sample D13 was extremely highly hydrophilized, Its contact angle with water is about 0. 'And the coating looks transparent and does not lose its uniformity. The solid content and transparency of the coating are soda-lime glass plates (40 X 100 × 2 mm) immersed in a titanium oxide sol diluted with ethanol ( ST-K01) solution to The soda-lime glass was pulled up at a pulling speed of 24 cm / min to complete the impregnation layer coating. The titanium oxide sol was diluted with ethanol to the following solid content == Then, the coating was heated at 50 × or 15〇τ to prepare Samples of this paper New York City Financial Standards (CNS "Α4 specifications (21GX_297 Gongchu). (Please read the precautions on the back first. Rl ^-write this page) ------------ Equipment-; ----- Order -42-4 6 7 94 3 Α7 Β7 V. Description of the invention (40) to E8. The turbidity meter (Hazegardplus, manufactured by Gardener) was used to measure the condition of these samples. The results are briefly described in the table below. Sample 12 3 4 5 6 Ε Ε Ε Ε Ε Ε Ε Ε Solid content (wt%) 10 5 10.1 10 5 1 0.1 Heat treatment temperature (0 50 50 50 50 150 150 150 150 150

混濁狀況 (% ) 5B 6B 9H 9H 6B 6B 8H 9H (請先閲讀背面之注意事項ί,ν·寫本頁) 貫例E2 塗層固體含量和硬度 以實例E1相同方法製備樣品E9至E16,而採以ST-K03. 為氧化鈦溶膠。以日本工業標準(JIS)H8602制訂之鉛筆 硬度測試方法測量這些樣品。結果簡要說明於下表。 ---赛------II----- 層 經濟部中央標準局員工消費合作社印製Haze (%) 5B 6B 9H 9H 6B 6B 8H 9H (Please read the precautions on the back first, write this page) Example E2 Coating solid content and hardness Prepare samples E9 to E16 in the same way as in Example E1, and Take ST-K03. As a titanium oxide sol. These samples were measured by a pencil hardness test method established by the Japanese Industrial Standard (JIS) H8602. The results are briefly described in the table below. --- 赛 ------ II ----- Floor Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs

樣品 固體含量 熱處理溫 鉛筆 (wt%) 度(。〇 度 Ε9 10 50 5B Ε10 5 50 6B Ε11 1 50 9H Ε12 0.1 50 9H Ε13 10 150 6B Ε14 5 150 6B Ε15 1 150 8H Ε16 0.1 150 9H 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) j 線-----乂 -43Sample solid content heat-treated warm pencil (wt%) Degree (0 ° E9 10 50 5B E10 5 50 6B E11 1 50 9H E12 0.1 50 9H E13 10 150 6B E14 5 150 6B E15 1 150 8H E16 0.1 150 9H Paper size Applicable to China National Standard (CNS) Α4 specification (210 × 297 mm) j line ----- 乂 -43

Claims (1)

申請專利範圍 第86110219號專利申請案申請專利範圍修正本 修正日期:89年06月 (请先閎讀背面之法意事項再填寫本頁) 1.—種使元件表面親水化之、纟且合物,其中包含至少 (a) 金屬氧化物光催化顆粒, (b) 至少一種..組成物’該組成物係擇自梦土微細 顆粒’可形成矽酮樹脂薄膜之先驅物和可形成梦薄 膜之先驅物所組成之族者,及 (c) 溶劑, 其中該矽薄膜先驅物為以下面平均組合物化學 式為代表之<5夕酸鹽: S ί Xq〇(4-ci)/2 訂 其十’ X代表烧氧基或鹵素原子’而q為滿足〇<q<4 之數目, 或為四官能基之可水解的梦烧衍生物,該衍生 物以下列化學通式代表: SiX4 且; 經濟部智慧財產局員工消費合作社印製 其中’該發酿I樹脂薄膜先驅物為以下面平均組 合物化學式為代表之矽氧烷: RPS i Χς〇(4-ρ-ς)/2 其中’ R係擇自由氫原子和一個或更多個有機官 能基所組成之族者; X代表烧乳基或函素原子,及 P為滿足0<p<2之數目,及q為滿足〇<(1<4之數目, 表紙張尺度適用中國國家標準(CNS〉A4祕(210X297公;^ 4^ 467943 AS B8 C8 D8 六 申請專利範園 M濟部智慧財產局員工消費合作社印製 戴為可水解之矽烷衍生物,該衍±物以下列化學通 式代表: RpSiX4-p R係擇自由氫原子和一個或更多個有機官能基所 組成之族者; X代表烷氧基或齒素原子,及 P為1或2 ; 其中’該叙合物令之光催化顆粒和矽土微細顆 粒或先驅物,換算為矽土之重量,之總含量為〇〇1 至5%重量比。 如申請專利範圍第1項之組合物,當該組合物應用至 元件表面,並給予該表面光線後,具有親水性,其 親水性’以表面與水之接觸角來表示,不超過丨〇。。 3. 如申請專利範圍第2項之組合物,其中,該表面與水 之接觸角為5。。 4. 如申請專利範圍第1項之組合物 之平均結晶直徑為lOOnm。 5. 如申請專利範圍第1項之組合物 由銳鈦礦氧化鈦所組成。 6. 如申請專利範圍第1項之組合物 料,該材料之折射率不超過2 » 7. 如申請專利範圍第1項之組合物,其中,該溶劑為醇 類。 8. 如申請專利範圍第7項之組合物,其中,該醇類為液 2· 其中’光催化顆粒 其中’光催化顆粒 其中更包含一個材 本紙張尺度適用中國國家梯準(CNS ) A4洗格(210 X 297公釐) 4 6 7 ^4 3 AS B8 C8 D«Application for Patent Scope No. 86110219 Patent Application for Patent Scope Amendment Date of this revision: June 89 (please read the legal notices on the back before filling out this page) 1. A kind of hydrophilization of the component surface Material, which contains at least (a) metal oxide photocatalytic particles, (b) at least one ... composition 'the composition is selected from the dream soil fine particles' a precursor for forming a silicone resin film and a dream film A family of precursors, and (c) a solvent, wherein the silicon thin film precursor is represented by the following average composition chemical formula: < 5th acid salt: S ί Xq〇 (4-ci) / 2 Order Its ten 'X represents a thiol or a halogen atom' and q is a number satisfying 0 < q < 4, or a hydrolysable dream-fired derivative of tetrafunctional group, which is represented by the following chemical formula: SiX4 And; Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, “The brewer I resin film precursor is a siloxane represented by the following average composition chemical formula: RPS i Χς〇 (4-ρ-ς) / 2 of which 'R is a free hydrogen atom and one or more A group of multiple organic functional groups; X represents a calcined lactyl group or a pheromone atom, and P is a number satisfying 0 < p < 2, and q is a number satisfying 0 < (1 < 4, table size Applicable to Chinese national standard (CNS> A4 secret (210X297); ^ 4 ^ 467943 AS B8 C8 D8 Six patent applications Fan Yuan M Ministry of Economic Affairs Bureau Intellectual Property Bureau Staff Consumer Cooperatives Printed as a hydrolyzable silane derivative, this derivative It is represented by the following chemical formula: RpSiX4-p R is a group consisting of a free hydrogen atom and one or more organic functional groups; X represents an alkoxy group or a halogen atom, and P is 1 or 2; where ' The composition allows the photocatalytic particles and silica fine particles or precursors to be converted to the weight of silica, and the total content is from 0.001 to 5% by weight. The composition is applied to the surface of a component, and after giving light to the surface, the composition is hydrophilic, and its hydrophilicity is expressed by the contact angle between the surface and water, not exceeding 丨 〇. Object, where the contact angle of the surface with water is 5. 4. The average crystal diameter of the composition in the scope of the patent application is 100 nm. 5. If the composition in the scope of the patent application is composed of anatase titanium oxide. 6. If the composition of the scope of the patent application is in item 1, The refractive index of the material does not exceed 2 »7. The composition as claimed in item 1 of the patent application scope, wherein the solvent is an alcohol. 8. The composition as claimed in item 7 of the patent application scope, wherein the alcohol is a liquid 2 · Among them, the photocatalytic particles among which the photocatalytic particles also include a material paper size applicable to China National Standards (CNS) A4 wash (210 X 297 mm) 4 6 7 ^ 4 3 AS B8 C8 D « 申請專利範圍 經濟部智慧財產局員工消費合作社印製 體醇類,其分子量為60至300 β 9,如申請專利範圍第8項之,組合物, 體醇類,其分子量為60至1〇〇。 10.如申請專利範圍第1項之組合物, 性劑。 如申請專利範圍第1 0項之組合物 性劑之含量少於1 〇份重量比,相 光催化顆粒。 如申請專利範圍第11項之組合物 性劑之含量為0.4至2份重量比, 之光催化顆粒。 13. 如申請專利範圍第1項之組合物, 14. 如申請專利範圍第1項之組合物, 含硬土微細顆粒,而該石夕土微細 捏範圍是1至1 〇 〇 nm。 15. 如申請專利範圍第1項之組合物, 含矽土微細顆粒,而該矽土微細 徑份為是5至50mn。 16. 如申請專利範圍第1項之組合物, 含矽土微細顆粒,而該矽土微細 徑份為是8至20 nm = 17. 如申請專利範圍第1項之組合物, 屬或其化合物》 18. 如申請專利範圍第1項之組合物, 其中,該醇類為 液 11 12 其t更包含界面活 ’其中’該界面活 對於一份重量比之 ’其中,該界面活 相對於一份重量比 其中更包含酸。 其令,該級合物包 顆粒之平均顆粒直 其中,該組合物包 顆粒之平均顆粒直 其中’該組合物包 顆粒之平均顆粒直 其中更包含抗菌金 其中更包含至少一 ί請先閱锖背面之注意事項再填寫本頁j ,\乂_ 訂 .i 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) Α8 Β8 C8 D8 &、申請專利範圍 個金屬’該金屬係擇自由鉑,鈀,铑,釕,餓,和 銥所組成之族者。 19_如申請專利範圍第i項之組合物,其中,該光催化氧 化物係擇自由銳鈦礦氧化鈦,金紅石鈦氧化鈦,氧 化鋅,氧化錫,氧化鐵,三氧化二鉍,三氧化鎢, 和鈦酸鏍所組成之族者。 20. 如申請專利範圍第丨項之組合物,當該組合物應用至 元件表面時,提供元件表面防霧性β 21. 如申睛專利範圍第1項之組合物,當該組合物應用於 元件表面’形成薄膜後’使得黏著於表面之濕氣凝 結的水或水滴分散於薄膜上,因此使得薄膜表面避 免因濕氣凝結的水及/或水滴造成起霧或混濁。 22. 如申請專利範圍第1項之組合物,當該組合物應用於 元件表面,形成薄膜後,黏著於表面之污染物容易 以水洗去。 23. —種氣霧劑組合物,其中包含如申請專利範圍第”頁 之組合物,和揮發劑。 24. —種元件表面親水化之方法,其中包含下面步驟: 將申請專利乾圍第1項之組合物應用於元件表面上;及 將該组合物乾燥或硬化。 25. 如申請專利範圍第24項之方法’其中,該元件是透 明的’而以此法得到之元件也是透明的。 26. —個具有親水性表面之元件’該元件係依照申請專 利範圍第2 4或2 5項之方法製造。 本紙張尺度適用中國國家糯準< CNS ) A4規格(210X297公疫) (請先閲讀背面之注意^項再填窝本頁) 訂 線、 經濟部眢慧財產局員工消費合作社印製 47Scope of patent application: Intellectual Property Bureau of the Ministry of Economic Affairs, Consumer Cooperatives printed body alcohols with a molecular weight of 60 to 300 β 9, as described in the scope of the patent application No. 8, the composition, body alcohols, has a molecular weight of 60 to 100. . 10. The composition according to item 1 of the scope of patent application, sex agent. If the content of the composition agent in item 10 of the scope of patent application is less than 10 parts by weight, the phase photocatalytic particles are used. If the content of the composition agent in the scope of application for item 11 is 0.4 to 2 parts by weight, the photocatalytic particles. 13. The composition according to item 1 of the scope of patent application, 14. The composition according to item 1 of the scope of patent application, containing fine particles of hard soil, and the fine kneading range of the stone evening soil is 1 to 1000 nm. 15. The composition according to item 1 of the patent application scope, which contains fine particles of silica, and the fine diameter of the silica is 5 to 50 mn. 16. If the composition of the scope of patent application item 1 contains fine particles of silica, and the fine diameter of the silica is 8 to 20 nm = 17. If the composition of the scope of patent application item 1 belongs to or a compound thereof 》 18. If the composition of the scope of application for the first item of the patent, wherein the alcohol is liquid 11 12 and t further includes interfacial activity 'wherein' the interfacial activity is relative to a weight ratio ', where the interfacial activity is relative to one Parts by weight contain more acid than this. It means that the average particles of the composition-coated particles are straight, the average particles of the composition-coated particles are included, the average particles of the composition-coated particles are included, and the antibacterial gold is further included. Please read 锖Note on the back page, please fill in this page j, \ 乂 _ order. I This paper size applies to Chinese National Standard (CNS) Α4 specification (210 × 297 mm) Α8 Β8 C8 D8 & patent application scope of metal 'the metal system selection A family of free platinum, palladium, rhodium, ruthenium, hungry, and iridium. 19_ The composition according to item i in the patent application range, wherein the photocatalytic oxide is selected from free anatase titanium oxide, rutile titanium titanium oxide, zinc oxide, tin oxide, iron oxide, bismuth trioxide, three Tungsten oxide, and thorium titanate. 20. If the composition of the scope of application for the patent application item 丨, when the composition is applied to the surface of the component, provide anti-fog property of the surface of the component β 21. If the composition of the scope of patent application for the first item, when the composition is applied to The element surface 'after film formation' allows moisture or water droplets condensed on the surface to disperse on the film, thereby preventing the film surface from being fogged or turbid due to moisture condensation water and / or water droplets. 22. If the composition of the scope of patent application No. 1 is applied, when the composition is applied to the surface of a component and a thin film is formed, contaminants adhering to the surface are easily washed away with water. 23. —An aerosol composition, which includes the composition as described in page “Patent Application”, and a volatile agent. 24. —A method for hydrophilizing the surface of an element, which includes the following steps: The composition of the present invention is applied to the surface of the component; and the composition is dried or hardened. 25. For example, the method of the 24th aspect of the patent application, wherein the component is transparent, and the component obtained by this method is also transparent. 26. —A component with a hydrophilic surface 'This component is manufactured in accordance with the method of item No. 24 or No. 25 of the scope of patent application. This paper size applies to China National Wax Standard < CNS) A4 specification (210X297 public epidemic) (please (Please read the note on the back ^ before filling in this page.)
TW86110219A 1996-07-19 1997-07-18 Photocatalytically hydrophilifiable coating composition TW467943B (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP22164196 1996-07-19
JP26655496 1996-08-31
JP28579696 1996-09-20
JP35595396 1996-12-24
JP1304897 1997-01-08

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8568870B2 (en) 2007-12-04 2013-10-29 Nichiha Corporation Coating film for building material
TWI477681B (en) * 2011-09-20 2015-03-21 Nichiha Co Ltd Construction boards, and construction boards

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8568870B2 (en) 2007-12-04 2013-10-29 Nichiha Corporation Coating film for building material
TWI477681B (en) * 2011-09-20 2015-03-21 Nichiha Co Ltd Construction boards, and construction boards

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