TWI225873B - Three-dimensional decorative product and its manufacturing method - Google Patents
Three-dimensional decorative product and its manufacturing method Download PDFInfo
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1225873 -------- 五、發明說明(1) 【技術領域— 本發明係有關由難黏合性基體材料播# 及立體裝舞件之製造方法 構成的立體裝飾件 夂八有稷雜結構之難黏合性基 早輛芩冲件類 及其製造方法。 何枓所構成的立體裝飾件 【先前技術】 車輛零部件多數採用矽氧樹酯、 酉旨、氨基甲酸乙酿樹醋類之難黏合;祕曰、聚乙稀樹 合性材科構成的·黏合性基體材料材表4面但二由上述難 水性或拒水性、所以一般難以彳在具有疏 刷、紫外線塗都類之表面處理。=別^構件黏合、印 料進行立體加工或使其發泡時,現===難黏合性材 表面結構複雜且不平滑,難md“生基體材料 體材料之表面特:,採===:構成的難黏合性基 偶合劑或鈦偶合劑類的方法二:j在其表面塗布矽烷 ^往往需較多量的底漆或梦炫偶合劑獲質效 的處理设備,處理時間亦較長 不僅而有特定 因此,作為替代塗底殊二王存在問題。 材料表面改質方法,目前』:研難巧合性基體 法、電暈放電處理、電I卢 法有.紫外線照射 光接枝法、喷砂法齊nf面職與感應基法、表面 面改質方法。續理及絡酸混合液處理等各種表 91082NKTISMJP-F016W. p t d 第4頁 1225873 五、發明說明(2) 厶成t制於日ί巧開平5 —68934號公報内,揭示有採用 :姑央衣造的尚壓水銀燈、對疏水性塑膠表面照射紫外 ,肉使,層的濕漂性及黏合性提高。美國專利第5〇986 1 8 有混合氣體氛圍中,對疏水性塑朦表面選擇性 及二:^⑽及託—波長之紫外線叫吏塗層之濕霜性 M 1 ° 冋。此外,日本特開平1 0 —67869號公報内, =表面,邊噴吹氣體、邊用高壓 電ΐίϊ尚=性’對聚稀煙樹脂等表面進行臭氧處理、 活性:處理之放電處理及紫外線照射等表面 疫里之後、使乙烯基單體接枝。 但係上述表面改質方法 、而且尚在乂 ^ ,負方法不僅表面特性之改質不充分 危險等琿境門:種問題:污染操作環境,冑可能產生 備規模大,二各:洗及廢水處理等操作問題,設 1貝格叩貴等經濟問題。 以考】對合: = f :表面改質方法,亦可 =指數或接觸角 果亦能長時間保拄$ 土 竹庄 < 改臭不充分,且效 報揭示般,對難斑i再者,如日本特開平9—^4810號公 存在有容易產生基體材料表面進行火焰處理時,仍 勿座生熱變形的問題。 提出=基it人等如de__26ai公報揭示般,亦 先對金屬或Ur之改質方法,該方法包含兩個步驟:首 ^破蹲製品的固體基體表面至少進行一焰 91082NKTISMJP-F016TW.ptd 1225873 五、發明說明(3) 處理’使該表面改質;再至少進行一次石夕氧化焰處理,使 s亥表面改質。採用此種固體基體表面改質方法後,固體基 體之表面就可確實地進行改質處理,即可獲得將印刷用油 墨或紫外線硬化型塗料牢固地黏合的效果。 但係’已公開的固體基體表面之改質方法,作為砍烧 化合物係單獨使用高沸點的四甲氧基矽烷(沸點丨22 t)類 之烷氧基矽烷化合物。若此類烷氧基矽烷化合物大量與空 氣等混合時,容易產生部分不完全燃燒的現像。此外,在 石夕氧化焰處.理前再包含另外的氧化焰處理步驟,因此對固 .體基體表面雖可獲得優良的改質效果,但其處理時間卻變 長。 因此’本發明者經過經心研究,結果發現:對由難點 合性材料構成的難黏合性基體材料進行立體加工或使直發 泡時,對於該難黏合性基體材料之表面,施以源自含 的火焰處理時、即可使難黏合性基體材 枓之表面進仃均勻且充分的改質、從而完成本發明。 亦即,本發明提供一種在立體加工的難黏合性 ?及其面上之發泡層或緩衝層(中間層)mi:: 牛固黏合的立體裝飾件及其製造方法。 I明摘述 〔1〕本發明在解決上述問 飾件,其特徵在於對立體加、P 、 ’、種立體裝 有中間層及裝部構件之立體梦::黏合性基體材料面上具 之立體裝飾件,在難黏合性基體表面1225873 -------- V. Description of the invention (1) [Technical Field — The present invention relates to a three-dimensional decorative piece composed of a hard-to-adhesive base material and a three-dimensional costume dance manufacturing method. Structurally difficult-to-adhesive stamping parts and their manufacturing methods. Three-dimensional decorative parts made by He Zhi [Previous technology] Most of the vehicle parts are made of silicone resin, succinct, and urethane ethyl vinegar, which are difficult to be bonded; Secret, polyethylene resin materials, etc. The surface of the adhesive base material is on the 4th side, but because of the above-mentioned water-repellent or water-repellent properties, it is generally difficult to apply the surface treatment with brushing and UV coating. = Don't ^ When the components are bonded, the printed material is three-dimensionally processed or foamed, it is now === The surface structure of the difficult-to-adhesive material is complex and not smooth, and the surface of the body material is difficult. : Method 2 for forming a difficult-to-adhesive base coupling agent or titanium coupling agent: j Applying silane on the surface ^ often requires a large amount of primer or Mengxuan coupling agent to obtain effective processing equipment, and the processing time is also long. Not only is it specific, therefore, there are problems as a substitute for coating. The method of surface modification of materials, currently ": difficult to coincide with the matrix method, corona discharge treatment, electric I Lu method. UV irradiation light grafting method, Sandblasting method, nf surface working method, induction-based method, surface surface modification method. Continued treatment and complex acid mixture solution treatment, etc. 91082NKTISMJP-F016W. Ptd Page 4 1225873 V. Description of the invention (2) In Japanese Patent No. 5-68934, it was revealed that the use of a high pressure mercury lamp made of Guyang clothing, ultraviolet light irradiation on the surface of hydrophobic plastic, meat, the wet bleachability and adhesion of the layer are improved. US Patent No. 5 986 1 8 Hydrophobic in mixed gas atmosphere The selectivity of the haze surface and the two: ^ ⑽ and the wavelength of the ultraviolet light is called the wet frost property of the coating M 1 ° 此外. In addition, in Japanese Patent Application Laid-Open No. 10-67869, = surface, while blowing gas, edge After high-voltage electricity is used to treat the surface of polysmoky resin and other ozone treatment, activity: treatment of the discharge treatment and ultraviolet irradiation, etc., the vinyl monomer is grafted. However, it is the above surface modification method However, the negative method is not only the surface quality of the surface is not adequately modified and dangerous, etc .: The following problems: pollution of the operating environment, which may produce large scale, two: operation problems such as washing and wastewater treatment, set 1 Economic problems such as Berger's expensive. To test] Conjunction: = f: surface modification method, can also = index or contact angle fruit can also protect for a long time $ 土 竹 庄 < inadequate deodorization, and effective report As revealed, for the difficult spot i, as in Japanese Patent Application Laid-Open No. 9- ^ 4810, there is a problem that the surface of the base material is not easy to generate heat when it is subjected to flame treatment. Revelation-like, but also to metal or Ur Modification method, the method includes two steps: firstly, the solid substrate surface of the broken product is subjected to at least one flame 91082NKTISMJP-F016TW.ptd 1225873 V. Description of the invention (3) Treatment 'improve the surface; at least once more stone After the oxidation flame treatment, the surface of the sea surface is modified. After adopting this solid substrate surface modification method, the surface of the solid substrate can be definitely modified, and the printing ink or ultraviolet curing coating can be firmly obtained. The effect of adhesion. However, it is a method of modifying the surface of a solid substrate that has been disclosed. As a chopping compound, an alkoxysilane compound of a high boiling point tetramethoxysilane (boiling point 22 t) is used alone. If such alkoxysilane compounds are mixed in a large amount with air, the phenomenon of partial incomplete combustion tends to occur. In addition, before the oxidized flame at Shixi, another oxidation flame treatment step is included. Therefore, although the surface of the solid substrate can be improved, the treatment time becomes longer. Therefore, the inventor's intensive research has found that when three-dimensional processing or direct foaming is performed on a difficult-to-bond base material composed of difficult-to-bond materials, the surface of the hard-to-bond base material is In the case of flame treatment, the surface of the non-adhesive base material can be uniformly and sufficiently modified, thereby completing the present invention. That is, the present invention provides a three-dimensionally-processed, hard-to-adhesive layer and a foam layer or a buffer layer (intermediate layer) on the surface of mi :: Niugu-adhered three-dimensional decorative pieces and a manufacturing method thereof. I. Abstract [1] The present invention is to solve the above-mentioned problem, which is characterized by three-dimensional addition, P, ', three-dimensional dream with three-dimensionally equipped with an intermediate layer and a component member: the surface of the adhesive matrix material has Three-dimensional decoration, on the surface of difficult-to-adhesive substrate
II mm $ 6頁 91082NKTlSMJP-F016TW.ptd 1225873II mm $ 6 pages 91082NKTlSMJP-F016TW.ptd 1225873
五、發明說明(4) 及中間層之表面,或任何一 合物之燃料氣體的火焰處理。表面,施以源自含矽烷化 亦即’藉由石夕氧仆抬卢:p田 適度改質,從而在立體加黏合性基體材料表面 之發泡層或緩衝層(中間層黏合性基體材料及其面上 黏合。 s 上’使裝飾構件能牢固地 〔2〕構成本發明之立體裝 或緩衝層。採用此干其中間層宜為發泡層 顯現適度緩衝性的立體裝飾件。P可提供立體感優良,且能 空殼成形。採立^裝飾件,其裝飾構件宜為粉末 有特殊形狀的裝飾構:就能提供立體感優良,且具 ^4〕構成本發日月之立體裝飾件、其難 氨基甲酸乙醋樹脂、氟碳烯^ ,設置j:: I至少一種樹脂構成。採用此種構成後 置;構!處’能夠牢固地將裝飾構件黏合;無設 置在飾構件處,露出基底時可顯示適度的剝離性。 > y 5〕構成本發明之立體裝飾件,其裝飾構件宜為由環 虱Μ脂、氯乙烯樹脂、丙烯酸樹脂、聚烯烴樹脂、 =酯樹脂或聚酯樹脂中至少一種樹脂構成。㈣此二構 成後,即可使用通用性強,價格低而且裝飾性優良 構件,其結果係可以提供價廉、裝飾性優良的立體裝: 〔6〕構成本發明之立體裝飾件,所使用的矽烷化合物5. Description of the invention (4) and the flame treatment of the surface of the intermediate layer or the fuel gas of any combination. On the surface, it is derived from silane-containing, that is, 'by Shi Xi's Oxygen: Lu moderately modified, so as to add a foam layer or a buffer layer on the surface of the three-dimensional adhesive matrix material (intermediate layer adhesive matrix material) It is bonded on its surface. S is used to make the decorative member firmly [2] constitute the three-dimensional device or buffer layer of the present invention. The dry intermediate layer should be a three-dimensional decorative piece that exhibits moderate cushioning in the foam layer. P 可Provide excellent three-dimensional effect, and can be formed into an empty shell. Adopt ^ decorative parts, the decorative member should be a decorative structure with a special shape of powder: it can provide excellent three-dimensional effect, and has ^ 4] to form the three-dimensional decoration of the sun and the moon Pieces, its hard urethane resin, fluorocarbonene ^, provided with at least one resin composition of j :: I. With this structure, it is placed at the back; the structure! Can't firmly adorn the decorative members; none is placed at the decorative members It can show moderate peelability when the substrate is exposed. ≫ y 5] constituting the three-dimensional decorative piece of the present invention, the decorative member thereof is preferably made of ring lice resin, vinyl chloride resin, acrylic resin, polyolefin resin, ester resin or Polyester resin At least one kind of resin composition. 构成 After these two kinds of composition, it can be used with strong versatility, low price, and excellent decoration. As a result, it can provide three-dimensional packaging with low cost and excellent decoration: [6] Three-dimensional decoration constituting the present invention Pieces, silane compounds used
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宜為使用沸點在1 Ο 〇 °c以下,且從烷基矽烷化合物、燒氧 基石夕院化合物及其改質物群中選擇至少一種化合物。使用 此,矽烷類化合物後,即使對於矽橡膠、氟橡膠或者係發 泡氨基甲酸乙酯材料類難黏合性基體材料之表面,裝飾4 件亦可牢固黏纟。而且,使用此種矽烷類化合物後,表面 改質的效果可長時間保持。 〔7〕構成本發明之立體裝飾件,其難黏合性基體材料 ί、、: H中間層表s,或係任一者表面之濕濡指數值(測 ί ί飾宜為在40_80dyn/cm範圍内。採用此種構成 後’裝飾構件即可極牢固地、長時間的粘合。 ~ 1 成本毛明之立體裝飾件,其構成的車輛零部件 ;=Γ義表板、車n、座椅、操作箱、内裝材料、伴 飾品而成的群體中至少選擇-種。採用此種 侔乂二πρ Γ提供一種裝飾性優&,且能顯示出與裝飾構 件之間牢固黏合強度的立體裝飾件。 币構 材上V且本古發士明之另一形態係在立體加工的難黏合性基體 =及裝飾構件之立體裝飾件的製造方法, 合性其^ i ί方法之特徵係包含有兩個步驟:在難黏 表面及中間層表面,或任-者之表面,施 間層之上方形成裝的火焰處理步驟以及在中 步驟亦:而”包含"化焰處理 可使裝飾構件牢固地‘人可仔適度改質,如此即 4 〇在立體加工的難黏合性基體材料It is preferable to use at least one compound having a boiling point of 100 ° C or less, and an alkylsilane compound, an oxygen-based oxalate compound, and a modified product group thereof. After using this, even if the surface of silicone rubber, fluororubber, or foamed urethane material is difficult to adhere to the base material, 4 pieces can be firmly adhered. In addition, the surface modification effect can be maintained for a long time after using such a silane compound. [7] The three-dimensional decorative part of the present invention, the hard-to-adhesive base material, the intermediate layer surface s, or the wet index value of any one of its surfaces (measurement should be in the range of 40_80dyn / cm Inside. After adopting this structure, the 'decorative member can be bonded very firmly and for a long time. ~ 1 Cost of Maoming's three-dimensional decorative parts, which constitute vehicle parts; = Γ table, car n, seat, Select at least one species from the group of operation boxes, interior materials, and accessories. Using this type of two πρ Γ provides a three-dimensional decoration with excellent decorative characteristics and showing strong adhesion strength with decorative members. Another form of V on the coin structure and the ancient ancient fascination is a three-dimensionally-processed, hard-to-adhesive substrate = and a method of manufacturing a three-dimensional decorative part of a decorative member. The characteristics of the method include two aspects. This step: forming a flame treatment step on the surface of the difficult-to-stick surface and the intermediate layer, or on the surface of any layer, above the interlayer, and the intermediate step is also: and "including" flame treatment can make the decorative member firmly 'Man can be moderately modified, so that is 4 〇 Hard-to-adhesive base material processed in three-dimensional
1225873 五、發明說明(6) Κϊί::發泡層或緩衝層(中間層)上,從而高效地製 上1〇〕實施本發明之立體裝飾件製造方法時,火焰之溫 為控制在500-1 50〇t範圍内。藉由如此實施,即可防 固:mi 完全燃燒’同時亦可使裝飾構件極為牢 層或緩衝声(中的難黏合性基體材料及其上方之發泡 有影燮,^可有γ t °此種火焰溫度雖㈣處理時間稍 i 1 止難黏合性基體材料之變形。 理時間宜為栌制二月之立體裝飾件製造方法時,火焰之處 件極為牢固地黏;in不完全燃燒,同時亦可使裝飾構 然對火焰溫上:如此火焰之㈣^ 料之變形。 θ 一可有效地防止難黏合性基體材 含?道飾件製造方法時,宜為再包 ,或任一者之表,* 口性基體材料表面及中間層表面 體的火焰處理步驟,源自不含矽烷類化合物之燃料氣 面所附著的垃ν或雜;’難黏合性基體材料表 揮矽氧化焰處理效果。、σ有效地除去,同時可有效地發 附圖簡單說明 相關的立體裝 第1圖係為用%… 於說明本發明第1實施形態 91082NKTISMJP-F016TW.ptd 1225873 五、發明說明(7) 飾件的圖。 第2圖係前部儀表板斜視圖。 第3圖係車門斜視圖。 ' 第4圖係座椅斜視圖。 · 第5圖係操作箱斜視圖。 第6圖係裝於車門上的内裝材料斜視圖。 ' 第7圖係保險桿斜視圖。 . 第8圖係車輛裝飾品斜視圖。 第9圖係用於說明本發明有關的立體裝飾件之製造方 法圖。 · 第1 0圖係用於說明表面改質裝置構造圖。 第11圖係用於說明火焰喷吹方法圖(之一)。 第1 2圖係用於說明火焰喷吹方法圖(之二)。 第1 3圖係用於說明火焰喷吹方法圖(之三)。 第1 4圖係用於說明表面改質裝置;火焰喷吹方法圖。 第1 5圖係用於說明攜帶型表面改質裝置圖。 第1 6圖係用於說明裝飾構件粉末空殼成形方法圖(之 第1 7圖係用於說明裝飾構件粉末空殼成形方法圖(之 _ 二)。 第1 8圖係用於說明裝飾構件層合方法圖(之一)。 第1 9圖係用於說明裝飾構件層合方法圖(之二)。 【實施方式】1225873 V. Description of the invention (6) Κϊί :: Foam layer or buffer layer (intermediate layer), so as to efficiently produce 10] When the three-dimensional decorative part manufacturing method of the present invention is implemented, the flame temperature is controlled to 500- In the range of 1500t. By doing so, it is possible to prevent solidification: mi is completely burned. At the same time, it can also make the decorative member extremely fast or cushion the sound (the difficult-to-adhesive matrix material and the foam above it have shadows, ^ t can have γ t ° Although the flame temperature is slightly longer than the processing time i 1 to prevent the deformation of the difficult-to-adhesive base material. The processing time should be the three-dimensional decorative part manufacturing method in February, where the flame parts are extremely sticky; incomplete combustion, At the same time, it can also make the decorative structure warm to the flame: such a deformation of the flame material. Θ One can effectively prevent the difficult-to-adhesive base material containing? In the method of manufacturing decorative parts, it should be repackaged, or either The table, * The flame treatment steps of the mouth surface of the base material and the surface of the intermediate layer are derived from the ν or impurities attached to the gas surface of the fuel containing no silane compounds; Effect., Σ is effectively removed, and the attached drawings can be effectively explained at the same time, and the related three-dimensional device is illustrated. The first picture is used for explaining the first embodiment of the present invention. 91082NKTISMJP-F016TW.ptd 1225873 V. Description of the invention (7) Trim Fig. 2 is a perspective view of a front instrument panel. Fig. 3 is a perspective view of a door. 'Fig. 4 is a perspective view of a seat. Fig. 5 is a perspective view of an operation box. Fig. 6 is a view of a door. Interior material perspective view. 'Fig. 7 is a perspective view of a bumper. Fig. 8 is a perspective view of a vehicle decoration. Fig. 9 is a view for explaining a method of manufacturing a three-dimensional decorative piece according to the present invention. · Fig. 10 The figure is used to explain the structure of the surface modification device. Figure 11 is used to explain the flame blowing method (Part 1). Figure 12 is used to explain the flame blowing method (No. 2). Figure 1 3 The drawing is used to explain the flame blowing method (No. 3). Figure 14 is used to explain the surface modification device; flame blowing method is shown. Figure 15 is used to illustrate the portable surface modification device. Fig. 16 is a diagram for explaining a method for forming a powdery hollow shell of a decorative member (No. 17 is a diagram for explaining a method of forming a powdery hollow shell of a decorative member (No. 2). Fig. 18 is a diagram for explaining a decorative member Lamination method diagram (part one). Fig. 19 is a diagram for explaining the lamination method of the decorative member (part two). [Embodiment]
91082NKTISMJP-F016TW.ptd 第10頁 122587391082NKTISMJP-F016TW.ptd Page 10 1225873
、以下參照附圖具體說明本發 方法之最佳實施形態。 明之立體裝飾件及其製造 〔第1實施形態〕 性基如第1圖所示’係經予立體加工的難黏^ 5。,具有中間層56及褒飾構件54之立體裝飾件 氣體:火I:者之表面,施以源自含矽烷類化合物之燃料 虱體的火焰處理(矽氧化焰處理)。 十 •立體加工的難黏合性基體材料 (1)種類Hereinafter, the best embodiment of the present method will be described in detail with reference to the drawings. Ming's three-dimensional decorative parts and their manufacturing [First Embodiment] As shown in Figure 1, the base is a three-dimensionally difficult to stick ^ 5. A three-dimensional decorative piece with an intermediate layer 56 and a decorative member 54. The surface of the gas: fire I: is subjected to a flame treatment (silicon oxide flame treatment) derived from a fuel containing silane compounds.十 • Three-dimensionally processed hard-to-adhesive base materials (1)
在第1實施形態中使用的難黏合性基體材料之種類並 ^予特別限制,可由以下樹脂群中至少選擇—種樹脂:氨 土 ^酸乙酯樹脂、氟碳樹脂、矽氧樹脂、聚酯樹脂、聚乙 烯樹脂、聚丙烯樹脂、改質聚丙烯樹脂、聚甲基戊烯樹脂 、聚醚樹脂、聚碳酸酯樹脂、聚醚砜樹脂、聚丙烯酸樹脂 聚鱗鱗gig树脂、聚醯亞胺樹脂、聚砜樹脂、聚苯乙烯樹 月曰 ♦醯私樹脂、聚苯硫_樹脂、乙浠-四I乙烯共聚物 、聚氟化乙烯樹脂、四氟乙烯-全氟醚共聚物、四氟乙烯〜 六氟丙烯共聚物、聚四氟乙烯樹脂、聚偏二氟乙烯樹脂、 欷二氟氯乙烯樹脂、乙稀-三氟氯乙烯共聚物、聚烯煙橡 膠、聚氨基甲酸乙酯橡膠、氟橡膠、矽氧橡膠、乙烯—丙 烯橡膠、乙烯-丙烯-二烯烴橡膠、苯乙烯類熱塑膠彈性體The type of the hard-to-adhesive base material used in the first embodiment is not particularly limited, and it can be selected from at least one of the following resin groups: ammonium urethane resin, fluorocarbon resin, silicone resin, polyester Resin, polyethylene resin, polypropylene resin, modified polypropylene resin, polymethylpentene resin, polyether resin, polycarbonate resin, polyethersulfone resin, polyacrylic resin, polyglycan resin, polyimide Resin, polysulfone resin, polystyrene resin, polystyrene resin, polyphenylene sulfide resin, acetamidine-tetraI ethylene copolymer, polyfluorinated ethylene resin, tetrafluoroethylene-perfluoroether copolymer, tetrafluoro Ethylene to hexafluoropropylene copolymer, polytetrafluoroethylene resin, polyvinylidene fluoride resin, vinylidene fluoride resin, ethylene-trifluorochloroethylene copolymer, polyolefin smoke rubber, polyurethane rubber, Fluorine rubber, silicone rubber, ethylene-propylene rubber, ethylene-propylene-diene rubber, styrene thermoplastic elastomer
!225873 五、發明說明(9) ”乙醋類熱塑性彈性體。 樹脂、聚丙=# L、別係接觸角大、濕濡指數小的聚乙烯 烯樹脂等、數对月曰三聚酯樹脂、聚碳酸酯樹脂、聚四氟乙 。 g由矽氧化焰處理後,可發揮優良的改質效果 、(2)填充材料 無機填 屬中選 、鉻、 為由下 氧化 鈣、石 玻璃、 種以上 聚酉旨 添加量 内,較 〜30重 料或ΐ:m j:材料中宜為再添加金屬材料、 擇-種或二丄此類金屬材料宜為由下列金 鎢、金、鋼、鐳、:°使用·崔呂、鎂、不鏽鋼、鎳 列材料中選擇一^舞、錫、錯等。無機填料宜 錯、氧化鋅、:::二種以上組合使用:氧化鈦、 灰、彿石、金1 1化錫、石夕石、滑石、碳酸 陶堯算。你Α ^ 鋼、鋅、鎳、錫、鉛、焊錫、 組合使用:^纖維宜為由下列纖維中選擇一種或二 纖維、聚· ί纖:U聚醯胺纖維、玻璃纖維、 ^ 義、准,金屬纖維,陶瓷纖維等。 相對=難釉人材料,無機填充料或纖維時,其整體 ^ 5性材料宜為控制在〇· 01〜80重量%笳Jfi 宜為控制在〇 P50舌”/ _㈤ ου更里/〇耗圍 量%範圍内。 重㈣範圍内’最較宜為控制在1 (3)形態 難黏合性基體材料之形態若為立體時即可,並未予特225873 V. Description of the invention (9) "Ethyl acetate-based thermoplastic elastomer. Resin, polypropylene = #L, other types of polyvinylene resin with large contact angle, small wet index, etc., several months, three polyester resins, Polycarbonate resin, polytetrafluoroethylene. G treated with silicon oxide flame, can show excellent modification effect, (2) filling material inorganic filler is selected, chromium, calcium oxide, stone glass, etc. Within the added amount of polyfluoric acid, more than ~ 30 heavy materials or ΐ: mj: materials should preferably be added with additional metal materials, and one or two kinds of metal materials should be composed of the following gold tungsten, gold, steel, radium ,: ° Use · Choo Lu, Magnesium, Stainless Steel, Nickel, etc. Choose one of Wu, Tin, W, etc. Inorganic filler should be W, Zinc oxide: :: Two or more combinations: Titanium oxide, ash, Buddha stone, gold 1 1 Fossil, sapphire, talc, carbonated ceramics. You A ^ steel, zinc, nickel, tin, lead, solder, combination: ^ fiber should be selected from one or two of the following fibers, poly · Fiber: U Polyamide fiber, glass fiber, ^, quasi, metal fiber, ceramic fiber Relative = difficult to glaze human materials, inorganic fillers or fibers, the overall ^ 5 materials should be controlled at 0.01 ~ 80% by weight 笳 Jfi should be controlled at 〇P50 tongue "/ _ ㈤υ 里 里 / 〇 consumption Within the range of%. Within the range of weight, it is most preferable to control the shape at 1 (3). The shape of the difficult-to-adhesive base material may be three-dimensional.
!225873 ---^~.— 五、發明說明(1〇) 宜為筒狀、柱狀、球狀、塊狀、内胎狀 :土狀:膜狀、纖維狀、織物狀、束狀等。如第=狀、 栌蚋邠儀表板1 〇 1、第3圖所示的車門丨〇 2、第4圖回—不 =3、第5圖所示的操作箱1〇4、第6圖所示的裝於:座 =内裝材料105、第7圖所示的保險桿1〇6以及第8圖:門上 名飾品1 0 7類之車輛零組件均可。 不的 ^難黏合性基體材料即使部分具有諸如板狀、# # — f狀、帶狀、長方狀、盤狀、繩狀類的平面結構 、: =此類難黏合性基體材料形態之變形例,宜為由=丄作 基體材料構成的立體結構物及金屬零件、陶瓷跫株^ 5性 零件、紙零件、木零件等把合構成的複合結構、破璃 2 ·中間層及裝飾構件 (1)中間層 中間層可以係底塗層或黏合改良層,亦 ,衝層。其理由係:採用底塗層或黏合改良層了‘泡,或 鬲難黏合性基體材料及裝飾構件間之黏合;3 β顯著提 J衝層後,可提供立體感優良,1具有適度:2層或 裝飾件。 及1野性的立體! 225873 --- ^ ~ .-- V. Description of the invention (10) It should be cylindrical, columnar, spherical, blocky, tube-shaped: soil-like: membrane-like, fiber-like, fabric-like, bundle-like, etc. As shown in the figure, the instrument panel 1 〇1, the door shown in Figure 3 丨 02, the return to Figure 4-No = 3, the operation box shown in Figure 5 and Figure 6 Shown installed in: seat = interior material 105, bumper 106 shown in Fig. 7 and Fig. 8: vehicle accessories of category 107 on the door. No, even if part of the hard-to-adhesive base material has a flat structure such as plate, # # — f-shaped, band-shaped, rectangular, disc-shaped, rope-like, etc .: = deformation of the shape of this hard-to-adhesive base material For example, it should be a composite structure composed of a three-dimensional structure composed of a base material and metal parts, ceramic parts, ceramic parts, paper parts, wood parts, etc., broken glass, intermediate layers, and decorative members ( 1) Intermediate layer The intermediate layer can be an undercoat layer or an adhesion-improving layer, or a punching layer. The reason is: the use of an undercoat layer or an adhesive improvement layer to 'bubble,' or the adhesion between difficult-to-adhesive base materials and decorative components; 3 β can significantly provide a three-dimensional feeling after the J layer is significantly improved, 1 has a moderate degree: 2 Layer or decoration. And a wild stereo
中間層之種類並未予特別限制,可採用& 樹脂、環氧樹脂、丙烯酸樹脂、矽烷偶合劑、$ =, 間層之厚度由其機能而$ ’若為底塗層或黏丄:s旨等 宜為在0.1〜100 範圍内;若為發泡層或緩°艮層 為在〇·1〜l〇mm範圍内。 曰寺’The type of the intermediate layer is not particularly limited, and resins, epoxy resins, acrylic resins, silane coupling agents, and $ = can be used. The thickness of the intermediate layer is determined by its function and $ 'if it is an undercoat or adhesive: s The purpose is preferably in the range of 0.1 to 100; in the case of a foamed layer or a gentle layer, it is in the range of 0.1 to 10 mm. Yuesi ’
1225873 五、發明說明(11) (2)裝飾構件 讀上飾+Ϊ件宜為由一種以上下列樹脂構成:J袁氧樹脂、 虱乙烯树知、丙烯酸樹脂、聚烯烴樹脂、氨基 月旨、聚碳酸S旨樹脂或聚s旨樹脂。其理由 = 使用通用性高、價廉,…飾性優 =。亦即,可提供價廉、裝飾性優良的立體裝飾 2 環氧樹脂。 冑且^級(+硬化狀態) .#裝飾構件之厚度宜為在10〜5 00 # m範圍内。1 .右此裝飾構件之厚度小於J 〇以m, /、 係 度及和耐久性將顯著降低。3 —方面,: 2:械二 度超過500# m時,則操作或黏合較曰遠/飾構件之厚 件之厚度較宜在25〜3GMm範圍^。困難。因此’裝飾構 考慮黏合性及操作方便,裝飾 薄片;考慮裝飾性更優&,表面 為平坦的 開口部(含切縫)。此外,裝飾構件理或設有 的印刷或著色。 之表面亦且為施以規定 裝飾構件如同第16圖(a) , ,宜為由粉末空殼成形。里理)及第17圖(aXC)所示 裝飾構件,則其立體感優/良:捭粉末空殼成形的 供從大尺寸(如:寬度達lm :持特殊形狀’且可以提1225873 V. Description of the invention (11) (2) The decorative element + decoration should be composed of more than one of the following resins: J Yuan oxygen resin, vinyl resin, acrylic resin, polyolefin resin, amino acid, polyamine Carbonic acid S resin or polys resin. Reasons = high versatility, low cost, ... good decoration =. That is, three-dimensional decorative 2 epoxy resin with low cost and excellent decorativeness can be provided.胄 And ^ grade (+ hardened state). # The thickness of the decorative member should be within the range of 10 ~ 5 00 # m. 1. The thickness of the decorative member is smaller than J 〇m, the system and durability will be significantly reduced. 3-Aspects: 2: When the mechanical degree exceeds 500 # m, the thickness of the thicker parts of the remote / decorative member for operation or bonding should be in the range of 25 ~ 3GMm ^. difficult. Therefore, the “decorative structure” considers the adhesiveness and the convenience of operation, and decorates the sheet; the decorative property is more excellent, and the surface is a flat opening (including slits). In addition, the decorative elements are printed or colored. The surface is also provided with a prescribed decorative member. As shown in Figure 16 (a), it should be formed from a powdered shell. Li) and the decorative member shown in Figure 17 (aXC), the three-dimensional sense is excellent / good: 捭 powder empty shell molding for large size (such as: width up to lm: holding a special shape 'and can be improved
Cm以下)為止任意尺寸的裝飾構件小上寸:寬度為10 17圖⑷〜(。)所示的粉末空殼成牛开;牛第16圖(a)〜(c)及第 战化步驟將在第2實施形態The size of the decorative member of any size up to Cm) is small: the width is 10 17 Figures 17 ~ (.) The powdered shell is opened as a cow; the cattle are shown in Figure 16 (a) ~ (c) and the warfare step will be In the second embodiment
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画丨· I 五、發明說明(12) 中詳細說明,在此省略。 3·燃料氣體 (1 )矽烷化合物 a·沸點 石夕烧化合物之彿點(常壓下)宜為控制在l〇〜i〇0 c範圍 内。其理由係:若係此類硅烷化合物之沸點未滿1 0 °c時, 2揮發性劇烈,有時操作困難。另一方面,當此類矽烷化 。物之/弗點超過1 0 0 C,則與空氣類之助燃氣體或助燃劑 f混合性即顯著降低1易造成我化合物不完全燃燒, k而使難黏&性基體材料之表面改質不均勻,難以長時間 質效果。因1^,此類石夕烧化合物之彿點較宜為控制 在15〜80Cfe圍内,更宜為控制在2〇〜6(rc範圍内。 社槿Ϊ ί在丨此類矽烷化合物之沸點即使受矽烷化合物自身 可進行調整。彿點較低的烧基石夕烧化合物 行調整。 70化β物可猎由適當的混合使用進 b.種類 石夕烧化合物之稽錮廿土工& …合物或貌氧基石夕別’例如可使用烧基 ,可與空氣等均句混二=,,加熱後容易氣化 基…合物可。… 化合物組合使用:…石夕貌、:::=用氣上 第15頁 91082NKTISMJP-F016TW.ptd 1225873 五、發明說明(13) 四甲基矽烷、1,2 —二苯基四甲基矽烷、丨 一 & 矽烷、1,2_二苯基四乙基矽烷、3 — ’一〆一氯四乙基 、1,2, 3 —三苯基四甲基矽烷、二甲基二 氯四甲基矽烷 此類烷基矽烷化合物中,四甲基土 一 基四石夕烷等。 於沸點特別低,易與空氣混合,係較:::二土矽烷由 2—二氯四甲基残類之_切烧化合物m物。!, 吳效果特別優&,亦係較宜的矽烷化合物。上於;、表面改 ,烷氧基矽烷化合物歸因於其酯結構,匕合物中 。但若係其沸點在1〇〜loot範圍"對:難占:,較高 ;料可發揮非常優良的表面改質效果,係較宜::性基體 合物。 权且的的矽烷化 C·平均分子量 用質譜儀測定時,矽烷化合物的平均分子 在50〜1 0 0 0範圍内。其理由# •且為控制 子里未滿50時,則揮發性高,操作困難。另一方面,* ^炫化合物平均分子量超過1〇〇〇,則加熱氣化,盥^ ί:Ϊ ί Ϊ f難。因此,用質譜儀測定時,矽烷化合:之 内:刀里且為控制在60〜500範圍内,較宜為7〇〜2〇〇範圍 d·密度 3 夕烧化合物在液體狀態下的密度宜為在0. 3〜〇 · 9克/ 範圍内。其理由係··若此類化合物之密度未滿〇· 3克/ cm3時,則,作時困難,且亦難以收藏在空氣溶膠罐中。另 一方面’若此類矽烷化合物之密度超過0. 9克/cm3時,則 第16頁 鴦 91082NKTISMJP.F016TW.ptd 1225873 --------— 五、發明說明(14) 氣化固難,同時者 等完全分離的狀:ί:工氣溶膠罐中時,會處於與.空氣 制在0.4〜〇.8克^7、ρ因此,矽烷化合物之密度值較宜為控 内。 克/CIH3範圍内,更宜為範圍 e ·添加量 合物量為100莫耳―e)%時,石夕烧化 係:若此類奸1〇,〜10莫耳%範圍内。其理由 有時未能顯現^ 加量未滿1Xl”莫耳%時,則 繼合二之添加量超過丨。莫耳%時,則 燃蜱不办入Ϊ = 5即降低,由此造成矽烷化合物 時二梦ί二人物此,當燃燒氣體之全部量為100莫耳% 更宜為1: ί二ίΐ添加量較宜為lx 10-9〜5莫耳%範圍内, 更且為lx 1〇8〜1莫耳%範圍内。 (2)助燃氣體 為可方便地控制火焰溫度’一般宜為在燃燒氣體中添 加助燃^體。此類助燃氣體有丙烷氣或天然氣類之烴類氣 體,或氲氣、氧氣、空氣類之助燃氣體。此外,當燃燒氣 體裝入空氣溶膠罐後使用時,此類助燃氣體宜為使用丙烷 氣及壓縮空氣等。 此外’當燃燒氣體之全部量為100莫耳(m〇le) %時, 此類助燃氣體之含有量宜為控制在8〇〜99.9莫耳(mole) % 範圍内。其理由係·當此類助燃氣體之含有量未滿8 〇莫耳Drawing 丨 · I 5. The detailed description in the description of the invention (12) is omitted here. 3. Fuel gas (1) Silane compound a. Boiling point The Buddha's point (under normal pressure) of the Shixiyan compound should be controlled within the range of 10 to 100 c. The reason is that if the boiling point of this type of silane compound is less than 10 ° C, the volatility is severe, and sometimes the operation is difficult. On the other hand, when such silanization occurs. If the material point is more than 100 ° C, the miscibility with air-based gas-supporting gas or combustion-supporting agent f will be significantly reduced. 1 It will cause incomplete combustion of our compounds, and k will cause the surface modification of difficult-to-stick & matrix materials. Non-uniform, difficult to qualitative effect for a long time. Because of 1 ^, the Buddha's point of this kind of Shixiyao compound is more preferably controlled within 15 ~ 80Cfe, and more preferably within the range of 20 ~ 6 (rc.). The boiling point of such silane compounds It can be adjusted even by the silane compound itself. The sintered compound with lower Buddha's point can be adjusted. 70 chemical β compounds can be used by appropriate mixing into b. Kinds of sieved compound with earthwork & ... For example, it is possible to use a sintered base, which can be mixed with air, etc., and it is easy to gasify the base after heating ... The compound is okay .... The compound is used in combination: ... Shi Xiwang, ::: = On the gas, page 15 91082NKTISMJP-F016TW.ptd 1225873 V. Description of the invention (13) Tetramethylsilane, 1,2-diphenyltetramethylsilane, 丨 & silane, 1,2_diphenyltetrazine Among the alkyl silane compounds such as ethylsilane, 3-'monochlorotetraethyl, 1,2,3-triphenyltetramethylsilane, and dimethyldichlorotetramethylsilane, tetramethyl earth One base of tetralithane, etc. It has a particularly low boiling point and is easy to mix with air. Methyl residues _ cut fired compounds m !, Wu effect is particularly good & also a more suitable silane compound. On the surface, the alkoxy silane compound is attributed to its ester structure, and However, if the boiling point is in the range of 10 ~ loot " yes: difficult to occupy :, higher; the material can play a very good surface modification effect, it is more suitable :: sex matrix compound. And the right silane When the average molecular weight of the silane is measured by a mass spectrometer, the average molecular weight of the silane compound is in the range of 50 to 100. The reason is # • When the molecular weight is less than 50, the volatility is high and the operation is difficult. Another On the other hand, if the average molecular weight of the compound is more than 1,000, it will be difficult to heat and gasify. Therefore, when measured with a mass spectrometer, the silane compound is within: within the knife and controlled to 60. Within the range of ~ 500, more preferably in the range of 70 ~ 200. D. Density 3. The density of the sintered compound in the liquid state is preferably in the range of 0.3 ~ 0.9g / range. The reason is ... if this When the density of the compound is less than 0.3 g / cm3, it is difficult to work, and it is difficult to store it in an aerosol can. Medium. On the other hand, if the density of such silane compounds exceeds 0.9 g / cm3, then page 16 鸯 91082NKTISMJP.F016TW.ptd 1225873 -------- V. Description of the invention (14) Gas It is difficult to solidify, and the other is completely separated: ί: When it is in an aerosol can, it will be in the air with 0.4 ~ 0.8 g ^ 7, ρ Therefore, the density value of the silane compound should be controlled within In the range of g / CIH3, it is more preferable to be in the range e. · When the amount of the added compound is 100 mol-e)%, the Shixi roasting system: if this kind of lumps are in the range of 10 to 10 mol%. The reason sometimes fails to show up. ^ When the amount is less than 1 × 1 "mol%, then the amount of the second combination exceeds 丨. When the molar amount is less than 5%, the flaming tick is reduced, resulting in silane. When the compound is two dreams, the two figures here, when the total amount of combustion gas is 100 mole%, it is more preferably 1: the addition amount of l2 is more preferably in the range of lx 10-9 to 5 mole%, and it is lx 1 〇8 ~ 1 Mole%. (2) The combustion-supporting gas is convenient to control the flame temperature. Generally, it is recommended to add combustion-supporting gas to the combustion gas. Such combustion-supporting gas is propane gas or natural gas-based hydrocarbon gas. Or tritium, oxygen, air and other combustion gas. In addition, when the combustion gas is used in an aerosol tank, such combustion gas should be propane gas and compressed air. In addition, when the total amount of combustion gas is 100 In the case of mole%, the content of such combustion-supporting gas should be controlled within the range of 80 to 99.9 mole%. The reason is that when the content of such combustion-supporting gas is less than 80%. Mol
91082NKTISMJP-F016TW.ptd 第17頁 1225873 五、發明說明(15) %時,則㈣化合物與线等的混合性即降低, 矽烷化合物燃燒不完全。另一方面,若此類助舞 有量超過99. 9莫耳% ’則有時未能顯現出對於難 體材料之改質效果。因此,當燃燒氣體之全部量為^基 耳%時,助燃氣體含有量較宜為在85〜99莫 里‘、、、其 更宜為在90〜99莫耳%範圍内。 旲耳/軏圍内, (3)載氣 為使矽烷化合物在燃燒氣體中充分混 氣。?即μ使錢化合物和載氣預先混合且^^ 即使在使用分不:: 藉由添加此類載氣, I穴$里較大,移動困難的矽烷化合物時,亦可 容易燃燒,能夠均丄八添加載氣,使矽烷化合物 面改質。此類較刀也貫施難黏合性基體材料之表 ,例如可使用* a載軋,係使用與助燃氣體同樣的氣體 。 二氣或氧氣、或丙烷氣或天燃氣等烴類氣體91082NKTISMJP-F016TW.ptd Page 17 1225873 V. Description of the invention (15)%, the miscibility of the europium compound and the thread will decrease, and the silane compound will not burn completely. On the other hand, if the amount of such dance support exceeds 99.9 mol%, it may sometimes fail to show a modification effect on difficult materials. Therefore, when the total amount of combustion gas is ^ mol%, the content of the combustion-supporting gas is more preferably in the range of 85 to 99 mol%, and more preferably in the range of 90 to 99 mol%. (3) Carrier gas In order to fully mix the silane compound in the combustion gas. ? That is, μ makes the compound and carrier gas mixed in advance and ^^ Even if it is not used: By adding such a carrier gas, when the silane compound is larger in size and difficult to move, it can be easily burned and can be evenly mixed. Add a carrier gas to modify the surface of the silane compound. This type of knife also applies the surface of difficult-to-adhesive matrix materials. For example, * a can be used for rolling, which uses the same gas as the combustion-supporting gas. Digas or oxygen, or hydrocarbon gas such as propane or natural gas
(4)添加物 a.種類 石夕烧以:::上的烧基♦烧化合物、烧氧 藉由如此添加彿點添加至燃燒氣體中。其理⑸ …占稍兩的化合物,作為與烷基矽烷化^(4) Additives a. Kinds Shi Xiyao burned with ::: ♦ Burning compounds, burning oxygen By adding Buddha points in this way, it is added to the combustion gas. The rationale… occupies slightly two compounds, as alkyl silanization ^
1225873 五、發明說明(16) 類之石夕燒化合物相、、六从托^ 烷化合物沸點低* 的的?文質辅助劑,可改善由於石夕 進-步提高難燃燒氣體之操作性不良,同時可 b.添:Γ性基體材料之表面改質效果。 ,力合物之全部量為1〇°莫耳%時,改質輔助劑之 ;:二2力.°乂5〇莫彻圍内。其理由係·:當此類改 ^7 ^ 5 Ο ^ X °/ Η± . 面若改質辅助劑之添加量 ί砂ί ΓIV則會產生燃燒氣體之不完全燃燒。因此 旦;ϋ:丨?之全部量為1〇°莫耳%時,改質輔助劑添加 置較宜為控制在0 i〜3〇簟耳叱鉻 2〇莫《範圍内。 耳^圍内’最宜為控制在〇.5〜 〔第2實施形態〕 第2貝轭形態如第9圖所示,係立體加工的難黏合性基 體材料58上具有中間層56及裝飾構件54之立體裝飾件5〇之 製造方法,其特徵係該製造方法包含下列步驟(丨)及(2 )。 (1) 於難黏合性基體材料58之表面及中間層56之表面, 或任一者之表面,實施源自含矽烷化合物之燃燒氣體的火 焰34之處理步驟(以下稱為矽氧化焰處理步驟)。 (2) 在中間層5 6之上方形成裝飾構件54的步驟(以下稱 為裝飾步驟)。 1 · 矽氧化焰處理步驟1225873 V. Description of the invention (16) Ishigaki compound phase, hexamethylene compound with low boiling point *? Cultural aids can improve the poor operability due to Shi Xi's further improvement of difficult-to-combustible gases, and at the same time b. Add: the surface modification effect of Γ-based matrix material. When the total amount of the strength compound is 10 ° Molar%, the reforming adjuvant is within the range of 2 °. 50 ° Mocher. The reason is: When such a change is ^ 7 ^ 5 Ο ^ X ° / Η ±. If the amount of the reforming additive is added ί 沙 ί ΓIV will produce incomplete combustion of the combustion gas. So once, ϋ: 丨? When the total amount is 10 ° Mole%, it is more suitable to control the addition of the reforming adjuvant to within the range of 0 to 30 mol Cr 2 Mo. Within the ear ^ 'is most preferably controlled within 0.5 ~ [Second Embodiment] The second yoke shape is shown in Fig. 9 and has a middle layer 56 and a decorative member on the three-dimensionally processed non-adhesive base material 58. The method for manufacturing a three-dimensional decorative member 50 of 54 is characterized in that the manufacturing method includes the following steps (丨) and (2). (1) A treatment step (hereinafter referred to as a silicon oxide flame treatment step) of a flame 34 derived from a combustion gas containing a silane compound is applied to the surface of the hard-to-adhesive base material 58 and the surface of the intermediate layer 56 or any of the surfaces. ). (2) A step of forming a decorative member 54 above the intermediate layer 56 (hereinafter referred to as a decorative step). 1 · Silicon oxide flame treatment steps
91082NKTISMJP-F016TW.ptd 第19頁 1225873 " 丨·· ___ 五、發明說明(17) (1 )燃燒氣體 及助:=與=實施形態中所說明者相同…化合物 乱體故在此省略再作說明。 (2)火焰處理條件 a·火焰溫度 内。匕:處之火焰溫度宜為控制在50°〜150°°c範圍 防止二ί ί此右該火焰溫度未滿5 00 °c時,則難以有效 防止夕炫化a物的不完全燃。一 ^ ^ 超過1 5 00 〇C時,則作A矣二 方面,§以火焰溫度 即右可&力a & ]作為表面改1對象之難黏合性基體材料 a Hi#、、、變形或熱劣化,如此即會過分限制可作為 ==;料之種類。因此,該火焰溫度較宜為二1 ^。5〇 12GGC範圍内,最宜為控制在6Q㈣…以下範圍 π* ^ ϋ #忒火焰溫度係在火焰之前端部測定所得的溫产 ,二燃燒氣體種類或燃燒氣體流量,或= 九,、粍耽體中的矽烷化合物種類或數量適當調節。 b ·處理時間 0 1 焰Λ理之火焰處理時間(喷射0寺間)宜為控制在 二:=:。其理由係:若該火焰處理時間未滿 改質效果另古 9地顯現出採用石夕燒化合物後的 ’當該火焰處理時間超過_秒時, ==質對象之難黏合性基體材料即有可能產生熱 ,支形或,,、、名化,如此即會過分限制可作為難黏合性基體材 第20頁 91082NKTISMJP.F016TW.ptd 1225873 五、發明說明(18) 料之種類。因此,火焰處理時間較宜為控制在〇· 3秒〜3〇秒 範圍内,最宜為控制在〇· 5〜20秒範圍内。 (3 )濕濡指數(表面能量) a·表面改質後91082NKTISMJP-F016TW.ptd Page 19 1225873 " 丨 ·· ___ V. Description of the invention (17) (1) Combustion gas and auxiliary: = same as that described in the embodiment ... Compound disorder is omitted here Instructions. (2) Flame treatment conditions a. Within flame temperature. Dagger: The flame temperature at the place should be controlled in the range of 50 ° ~ 150 °° c. To prevent this, when the flame temperature is less than 5 00 ° c, it is difficult to effectively prevent the incomplete combustion of the object. When ^ ^ exceeds 1 500 ° C, the second aspect is A 矣. § Take the flame temperature, which can be right & force a &] as the surface-changeable difficult-to-adhesive matrix material a Hi # ,,, deformation Or thermal degradation, which would be too restrictive, can be used as ==; the type of material. Therefore, the flame temperature is preferably 2 1 ^. Within the range of 5〇12GGC, it is most suitable to control within 6Q㈣ ... The following range π * ^ ϋ # 忒 The flame temperature is the temperature production measured at the end of the flame, the type of combustion gas or the flow rate of the combustion gas, or = 9 ,, 粍The type or amount of the silane compound in the body is appropriately adjusted. b. Processing time 0 1 The flame processing time of the flame Λ (spray 0 temple) should be controlled in two: = :. The reason is: if the flame treatment time is not enough, the modification effect will appear another 9 after the use of the stone firewood compound. 'When the flame treatment time exceeds _ seconds, == difficult to adhere to the substrate May generate heat, branch or ,,,, and name, so that it will be overly restricted. It can be used as a difficult-to-adhesive substrate. Page 20 91082NKTISMJP.F016TW.ptd 1225873 V. Description of the invention (18) The type of material. Therefore, the flame treatment time is preferably controlled in the range of 0.3 to 30 seconds, and most preferably controlled in the range of 0.5 to 20 seconds. (3) Wet index (surface energy) a. After surface modification
。表面改質後的難黏合性基材料之濕濡指數(測定溫度 25C)宜為控制在40〜8〇dyn/cm範圍内。其理由係··若此類 難黏合性基體材料之濕濡指數未滿45dyn/cm,則難以方便 地實施黏合,印刷及塗裝操作。另一方面,當此類難黏合 性基體材料之濕濡指數超過80dyn/cm時,由於過分實施表 面處理,有可能使難黏合性基體材料熱劣化。因此表面改 質後的,黏合性基體材料之濕濡指數較宜為控制在45〜75 dyn/cm範圍内,更宜為控制在μ〜圍内。 b·表面改質前. The wet index (measurement temperature 25C) of the hard-to-adhesive base material after surface modification should be controlled within the range of 40 to 80 dyn / cm. The reason is ... If the wet index of such hard-to-bond base materials is less than 45 dyn / cm, it is difficult to easily perform bonding, printing, and coating operations. On the other hand, when the wet index of such a non-adhesive base material exceeds 80 dyn / cm, the surface treatment may be excessively performed, and the non-adhesive base material may be thermally deteriorated. Therefore, after the surface modification, the wetness index of the adhesive matrix material is preferably controlled within the range of 45 to 75 dyn / cm, and more preferably controlled within the range of μ ~. b. Before surface modification
州ΐ二改質前的難黏合性基體材料之濕漂指數(測定溫 又C)且為控制在20〜45dyn/cm範圍内。其理由係:若J 類難黏合性基體材料之濕濡指數未滿2〇dyn/cm,則長時方 實施表面處if後,有可能使難黏合性IThe wet bleaching index (measurement temperature and C) of the difficult-to-adhesive base material before the modification of the state Ⅱ was controlled within the range of 20 to 45 dyn / cm. The reason is that if the wet index of the J-type hard-to-adhesive base material is less than 20 dyn / cm, the long-term implementation of if on the surface may make the hard-to-adhesive I
一方面’當此類難黏合性基體材料之㈣指數超 ; 可能難以用火焰有效地進行表面處理。例如 刖聚乙烯樹脂之濕漂指數約為4〇dyn/cm,採用石” 化焰處理溫度,進行约彳务丨、妒Μ ^ 可楛-5的二 的矽氧化焰處理,濕漂指數 : = 以上。因此,表面改質前(表面〇 刖)難黏"性基體材料之濕漂指數(測定溫度25。〇較宜On the one hand, when this kind of difficult-to-adhesive matrix material has an excessively high index; it may be difficult to effectively surface-treat with a flame. For example, the polyethylene resin has a wet drift index of about 40 dyn / cm, and is treated with a silicon "chemical flame" treatment temperature to perform the work. The oxidized silicon dioxide flame treatment is performed at a temperature of about 5%, and the wet drift index is: = Above. Therefore, before the surface is modified (surface 0 刖), it is difficult to adhere to the "wet bleaching index" of the matrix material (the measurement temperature is 25 °).
91082NKTISMJP-F016TW.ptd 1225873 五、發明說明(19) 為控制在25〜38dyn/cm範圍内,- a 範圍内。 又且為控制在28〜36dy.n/Cm (4 )接觸角 a.表面改質後 表面改質後的難黏合性基體鉍 (測定溫度25 °C )宜為在0.卜30 t 水所測定的接觸角 此類難黏合性基體材料之接觸角乾?。其理由係:若 實施表面處理,有可能使難黏合乂。,則由於過分 能難以方便地實施黏合、印刷過3门〇。,則可 “範“控制在°.5〜2°。。範圍内,更宜為控制在:〜 斑人ΐν系列示採用25 °c基準液測定所得的表面處理前雜 =生基體材料之濕儒指數(dyn/cm)及表面處理後(二難 y 、黏合性基體材料之濕濡指數測定例。 b·表面改質前 表面改备則(表面處理前)的難黏合性基體 測定的接觸角(測定、、田译9 ς。广、—法^ & 叶用水所 圍内。直理=Γ度25 ◦ m制在在50〜120°c範 50。時,則難以有效地用火焰進行表面處理。另鴻 基體材料之接觸角超過12°。日夺,由於長 、Ά ^ ^ 处理,有可能使難黏合性基體材料熱劣化 第22頁 91082NKTISMJP.F0l6TW.ptd 1225873 五、發明說明(20) 例如改貝處理刖的聚四氟乙烯樹脂之接觸角約丨〇 8。,利 用矽氧化焰處理之溫度等,進行約1秒鐘之石夕氧化焰處, Πί觸角降低至約2〇。以下。因此,表面改質前(表面 地1别)之難黏合性基體材料用測定的接 控制在6。〜11〇。範圍内,更宜為控制在8。〜1〇()。範圍内為。 (5 ) 表面改質裝置 宜為使用如第1 0圖所示的難黏合性基體材料表面改質 裝〒〇 ’該裝置主要包含以下三部分:貯藏矽烷化合物14 之財罐1 2、輸送燃料氣體之輪送部2 4、噴吹燃料氣體火焰 3 4之喷射部3 2。 a.貯罐 如第1 0圖所不,宜為具備有加熱手段16之貯藏矽烷化 L二4雄的ί1貯罐12 ’以及貯藏壓縮空氣類之助燃氣體的 第。罐(未予圖示)。在該例中,第1貯罐1 2之下方設有由 加熱器或導熱線,或連接於熱交換器之加熱板進行加埶的 加熱手段16 ’宜為在常溫,常壓狀態下將液狀矽烷化合物 氣化。 在對難黏合性基體材料進行表面處理時,宜由加敎 手段16將第1貯罐12内矽烷化合物14加熱至指定溫度,在”、 使之,化的狀態下與助燃氣體(空氣)混合,形成燃燒氣體 。此外,燃燒氣體中矽烷化合物之含有量極為重要,因此 宜對對該矽烷化合物之含有量進行間接控制,在第丨貯罐 12上設置壓力計(或係液面水平計)18,監視矽烷化合物蒸91082NKTISMJP-F016TW.ptd 1225873 V. Description of the invention (19) is controlled within the range of 25 ~ 38dyn / cm, within the range of -a. In addition, in order to control the contact angle at 28 ~ 36dy.n / Cm (4) a. After surface modification, the surface-modified hard-to-adhesive bismuth substrate (measurement temperature 25 ° C) should be at 0. 30 t The contact angle of this kind of difficult-to-bond base material is dry. . The reason is that if surface treatment is performed, it is possible to make it difficult to adhere to concrete. However, it can be difficult to easily implement gluing and printing over 3 doors due to excessive pressure. , You can control the "Fan" in °. 5 ~ 2 °. . Within the range, it is more suitable to control: ~ The spotted ΐν series shows that the surface impurity before the surface treatment measured with a 25 ° c reference solution = the wet rude index (dyn / cm) of the raw matrix material and the surface treatment (secondary y, Example of the measurement of the wet index of an adhesive substrate. B. Contact angles for difficult-to-adhesive substrates measured before surface modification (before surface treatment) (measurement, translation, and method 9) The leaf is surrounded by water. Straightening = Γ degree 25 ◦ When the m is in the range of 50 ~ 120 ° c and range 50. It is difficult to effectively use flame for surface treatment. In addition, the contact angle of the base material exceeds 12 °. It is possible to thermally degrade the difficult-to-adhesive base material due to long and long ^ ^ treatment. Page 22 91082NKTISMJP.F0l6TW.ptd 1225873 V. Description of the invention (20) For example, contact angle of polytetrafluoroethylene resin modified with osmium About 丨 〇8. Using the temperature of silicon oxide flame treatment, etc., for about 1 second at the oxidized flame of the stone eve, the antenna angle is reduced to about 20% or less. Therefore, before the surface modification (surface 1) The adhesion of the difficult-to-adhesive matrix material is controlled to be in the range of 6. to 110. Within the range, it is more preferably controlled within the range of 8. to 10 (). (5) The surface modification device is preferably a surface modification device using a difficult-to-adhesive substrate material as shown in Fig. 10 The device mainly includes the following three parts: a tank 1 for storing silane compound 14 2, a rotating part for conveying fuel gas 2 4, and an injection part 32 for blowing fuel gas flame 3 4. a. The storage tank is as shown in Fig. 10 No, it is preferably the first storage tank 12 'having a silanized L 2 4 male with heating means 16 and a storage tank for compressed gas such as compressed air (not shown). In this example, the first storage Below the tank 12 is provided a heating means 16 'for heating by a heater or a heat conducting wire, or a heating plate connected to a heat exchanger, preferably to vaporize the liquid silane compound at normal temperature and pressure. When the surface of the difficult-to-adhesive substrate is subjected to surface treatment, the silane compound 14 in the first storage tank 12 should be heated to a predetermined temperature by the adding means 16 and mixed with the combustion-supporting gas (air) in a state of "", and formed into a mixture. Combustion gas. In addition, the content of silane compounds in the combustion gas is extremely heavy. It is necessary to indirectly control the content of the silane compound. A pressure gauge (or liquid level meter) 18 is provided on the storage tank 12 to monitor the evaporation of the silane compound.
第23頁 I225873Page 23 I225873
五、發明說明(21) A壓(或矽烧化合物量) a· 輸送部 輪送部如第10圖所示,一般係管狀結 將來自筮1目令9 A Α 饰运邵具有 自苐1財罐12之石夕院化合物14及來自第 =)的助燃氣體(空氣)均勻混合’ * 未予圖 合室2 2,回拄且女m 〜风微麂軋體之混 控制燃燒氣體壓力之壓力計28。 机里计、或用於 柊批ί外’當矽烷化合物及助燃氣體均勻混合後,A --=製流量’ s為在混合室22上設置 f ::嚴 留時間之攆板。 永及用於延長停 b·噴射部 如第1 0圖所示,噴射部宜為具有將由 體,而得的火焰34喷吹在被處理物難黏 予特別限制,惟可選用下列型式的任 ^類雖未 ^擴散型喷射部、部分預混合型喷射部:匕=射 蒸發噴射部、粉煤噴射料。此外,切=^射。卜 特別限定,可如第1 〇胃^ ^ 形心亦未予 j戈弟UJ圖所不,朝向刖端部取 形結構;亦可如第丨】_张-士 而丨擴開,整體呈扇 向排列。噴射邻5 Γ二ί:方形,喷射口64橫 4 貝% 口丨之配置,即咱射部之邴婆 _ 理物難黏合性基體材料矣- ,且為考慮被處 抑口丨土签殿材枓表面改質之方 如·可如第1 2圖所示,沿圓形或橢圓形配置;匕疋。例 圖所示,在被處理物難黏合性基體币;、ϋ如第11 外,可如第13圖⑷所示,在被處理』置。此 難黏合性基體材料V. Description of the invention (21) A pressure (or amount of silicon sintered compound) a. The conveying part of the conveying part is shown in Figure 10. Generally, the tubular knot will come from 筮 1 目 令 9 A Α 运 运 绍 有 自 苐 1 The compound 14 of Shixiyuan of Caitan 12 and the combustion-supporting gas (air) from No. 1) are uniformly mixed. Pressure gauge 28. It can be used in the machine or externally. When the silane compound and the combustion-supporting gas are uniformly mixed, A-= the production flow rate s is a slab that sets f :: strict retention time on the mixing chamber 22. For the extended stop b. The spraying section is shown in Fig. 10. The spraying section should have a flame 34 that blows the substrate. It is difficult to stick to the object to be treated. However, any of the following types can be used. Although the type is not ^ diffusion type injection part, part of the pre-mixed type injection part: dagger = injection evaporation injection part, pulverized coal injection material. In addition, cut = ^ 射. It is specially limited, and can be shaped toward the end of the iliac crest as shown in the 10th stomach ^ ^ and the center of gravity is not shown in the figure of J Gedi UJ; it can also be expanded as shown in section 丨】 _ 张-士 而 丨Fan direction. Spray neighbouring 5 Γ2: square, spray port 64 horizontal 4 shell% 丨 The configuration of the mouth, that is, the grandmother of our department _ physical difficult to adhere to the base material 矣-, and to consider being suppressed 丨 soil signature hall The surface modification of the wood rafters can be arranged along a circle or an oval as shown in Figure 12; For example, as shown in the figure, it is difficult to adhere to the base material of the object to be processed; as shown in Figure 11, except that it can be placed in the processed object. This difficult-to-adhesive matrix material
91082NKTISMJP.F016TW.ptd 第24頁 122587391082NKTISMJP.F016TW.ptd Page 24 1225873
五、發明說明(22) 之單側僅離開一定距離西 被處理物難黏合性基體材;:亦可如第13圖⑻所示’在 。 ’斗之兩侧分別離開一定距離配置 C.形態 難黏合性基體材料表 所示,係將貯罐12、輸送辦^置之形態,可如第10圖 燒氣體而得的火焰而用之輸送部24與嘴吹由燃 在載置於如第“圖所示;=3組裝而成…卜,宜為 ,使被處理物難黏合上的固Μ具38之狀態下 表面改質裝置10,可以火焰34。此種組裝型之 性基體材料實施表面改^ 4效率的對被處理物難黏合 pH:如第15圖所示,宜為將難黏合性基體材料“ ;2^為攜帶型。即係:如虛線所圍的領域:Ϊ面 備h有肖式貯罐46、g己管管件47及不’ :44、再於配管管件47之前端部備有噴射部32。如 後,可使箱子44適當地移動,從而可對置於室 ,成 :或者大面積、大容量的被處理物方 =理 為便:運送箱子44,可在箱子44之上部安裝把手或=。 或將相子44之總重量作成20公斤以下。 —澠, 2.裝飾步驟 (1)裝飾構件 裝飾步驟所使用的裝飾構件需具立體感及形態優良V. Description of the invention (22) The one side of the invention is only a certain distance away from the substrate to be treated. 'The two sides of the bucket are arranged at a certain distance from each other. C. The form of the substrate with difficult-to-adhesive form, as shown in the table, is the form in which the storage tank 12 and the conveying device are placed, which can be used for conveying the flame obtained by burning the gas as shown in Figure 10. The part 24 and the mouth blow are assembled by being placed on the surface as shown in the "Figure; = 3 ...", preferably, the surface modification device 10 in a state where the fixture 38 is difficult to adhere to the object to be processed, You can flame 34. This assembly type of base material is difficult to adhere to the treated object with surface modification ^ 4 Efficiency: As shown in Figure 15, it should be difficult to adhere to the base material "; 2 ^ is portable. That is, the area enclosed by the dashed line: the front surface is provided with a Shaw tank 46, a tube fitting 47 and a non-'44, and a spraying portion 32 is provided at the front end of the piping fitting 47. After that, the box 44 can be appropriately moved, so that it can be placed in the room oppositely, so that it can be a large-area, large-capacity object to be processed: It is convenient to transport the box 44, and a handle can be installed on the upper part of the box 44 or = . Or make the total weight of Aiko 44 less than 20 kg. — 渑, 2. Decoration step (1) Decoration member The decoration member used in the decoration step must have a three-dimensional appearance and good shape.
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且可選擇任意的尺寸,因此宜為選用如第16圖(a)〜(c)及 第17® (a)〜(〇所例示的粉末空殼成形之裝飾構件。 第1 6圖(a)係採用以氣體或電源作為加熱源之加熱裝 置86 ’對具有成形面85之金屬製空殼金屬模82進行加熱的 步驟。宜為將空殼金屬模8 2加熱至粉末樹脂熔融的溫度。 所使用的空殼金屬模82之成形模84的成形面85,其形狀宜 為依所製作的樹脂成形品形狀而決定。 第16圖(b)係將加熱後的空殼金屬模82及收容有流動 狀粉末樹脂92之備用罐88,在成形模84之成形面85朝下、 備用罐88之開口面朝上的狀態下,使之一體聯結的步驟。 第16圖(c)係使空殼金屬模82及備用罐88旋轉,於空 殼金屬模82之成形模84的成形面85上,形成指定厚度之樹 脂膜94的步驟。亦即,宜為使空殼金屬模82及備用罐8 8上 下反轉。其理由係:備用罐88内的粉末樹脂92依靠自重落 在成形模8 4之成形面8 5上,因此接觸成形面8 5之樹脂及層 合的該部分樹脂係依成形模84之熱量形成熔融狀態,作為 表層而附著於成形面85。 第17圖(a)係在成形模84上形成指定厚度之樹脂膜94 的狀態下,將備用罐88由空殼金屬模82處拆卸的步驟。 第1 7圖(b)係採用水冷或空冷類之冷卻手段9 8,對空 殼金屬模82整體或成形模84之部分進行冷卻,從而使樹脂 模9 4硬化的步棘。 第1 7圖(c)係將樹脂膜9 4由形成模8 4上剝離,即脫模 步驟。And can choose any size, so it is suitable to choose the decorative member formed by powder shell as illustrated in Figures 16 (a) ~ (c) and 17® (a) ~ (〇. Figure 16 (a) A heating device 86 'using a gas or a power source as a heating source is a step of heating a metal shell mold 82 made of metal having a molding surface 85. It is preferable to heat the metal shell mold 82 to a temperature at which the powder resin melts. The shape of the molding surface 85 of the molding die 84 of the hollow shell mold 82 used should be determined according to the shape of the resin molded product. Figure 16 (b) shows the heated hollow shell mold 82 and the housing The backup tank 88 of the fluid powder resin 92 is a step of connecting the one body with the forming surface 85 of the molding die 84 facing downward and the opening surface of the backup tank 88 facing upward. Fig. 16 (c) shows an empty case. The step of rotating the metal mold 82 and the spare tank 88 to form a resin film 94 of a specified thickness on the forming surface 85 of the forming mold 84 of the empty shell metal mold 82. That is, it is preferable to make the empty shell metal mold 82 and the backup tank 8 8 The upside down. The reason is that the powder resin 92 in the reserve tank 88 falls on the molding by its own weight. The forming surface 8 5 of 8 4 is in contact with the resin of the forming surface 85 and the laminated resin part is formed into a molten state by the heat of the forming die 84 and adheres to the forming surface 85 as a surface layer. Fig. 17 (a) It is a step of disassembling the spare tank 88 from the empty shell metal mold 82 with the resin film 94 of a specified thickness formed on the molding die 84. Fig. 17 (b) is a cooling method using water cooling or air cooling 9 8 , Cooling the whole of the shell metal mold 82 or the part of the forming mold 84 to harden the resin mold 94. Fig. 17 (c) shows the resin film 94 is peeled off from the forming mold 84, that is, Demolding step.
91082NKTISMJP.F016TW.ptd 第26頁 1225873 五、發明說明(24) (2 )層合步驟 於將裝飾構件5 4層合至難黏合性基體材料5 8上時,如 第1 8圖所示,宜為先形成中間層5 7。例如,宜為先進行塗 底處理或係設置接著強度調整層。 但為使步驟更簡便、快速,如第1 9圖所示,宜為將作 為中間層5 7原料之材料形成於難黏合性基體材料5 8上後, 再將裝飾構件54層合於其上,在如此的狀態下藉由加熱或 照射紫外線,使裝飾構件54之黏合固定及中間層5 7之形成 同時實施。 貫施例 〔實施例1〕 1 ·立體裝飾件之製造 備妥已立體加工的難黏合性基體材料 亦即,備91082NKTISMJP.F016TW.ptd Page 26 1225873 V. Description of the invention (24) (2) The laminating step is to laminate the decorative member 54 to the hard-to-adhesive base material 58, as shown in FIG. 18, which is preferably Firstly, an intermediate layer 5 7 is formed. For example, it is preferable to perform a primer treatment first or to provide a strength adjustment layer next. However, in order to make the steps easier and faster, as shown in FIG. 19, it is preferable to form the material used as the raw material of the intermediate layer 5 7 on the difficult-to-adhesive base material 5 8 and then laminate the decorative member 54 thereon. In such a state, the bonding and fixing of the decorative member 54 and the formation of the intermediate layer 57 are performed simultaneously by heating or irradiating ultraviolet rays. Implementation Examples [Example 1] 1. Manufacture of three-dimensional decorative parts Prepare the three-dimensionally processed hard-to-adhesive base material, that is, prepare
丙烯製的車輛用前部儀表板基體材料。然後,對該車輛斥 前部儀表板基體材料之表面進行矽氧化焰處理。亦即,, ,體材料進行源自含矽烷化合物之燃料氣體的火焰處理: 每單位面積100cm2實施〇·5秒鐘)30秒鐘,使中間層及 構件能夠牢固黏合。 θ A > 然後,塗布發泡氨基甲 。隨後在3 0〜6 0 °C、1〜5分鐘 發泡氨基甲酸乙酯劑發泡, 輛用前部儀表板。 酸乙酯劑,同時形成裝飾構件 的件下加熱,使作為中間層之 同時使裝飾構件黏合,形成車Acrylic vehicle front panel base material. Then, the surface of the vehicle front panel base material was subjected to a silicon oxide flame treatment. That is, the body material is subjected to a flame treatment of a fuel gas derived from a silane compound: per unit area of 100 cm 2 (0.5 seconds) for 30 seconds, so that the intermediate layer and the components can be firmly adhered. θ A > Then, foamed urethane was applied. Then at 30 ~ 60 ° C for 1 ~ 5 minutes, the foaming urethane agent is foamed, and the front dashboard of the vehicle is used. Ethyl acetate agent, while heating the parts that form the decorative member, make the decorative member as an intermediate layer while bonding, forming a car
91082NKTISMJP-F0l6TW.ptd 第27頁 1225873 五、發明說明(25) 2 ·難黏合性基體材料之評估 採用標準液’測定已實施矽氧化焰處理後的階段車輛 用前部儀表板基體材料之濕漂指數。 再採用同樣方法測定已實施矽氧化焰處理前的車輛用 前部儀表板基體材料之濕濡指數。 3 ·立體裝飾件之評估 對車輛用前部儀表板基體材料上形成發泡氨基甲酸乙 酯層及裝飾構件後所得的車輛用前部儀表板,按照棋盤方⑯ 格試驗(JIS標準)測定裝飾構件之剝離強度,並按以 基準進行評估。 ◎ : 1 0 0個棋盤方格試驗中,完全未剝離; 〇:100個棋盤方格試驗中,剝離數為卜2個; △ : 1 0 0個棋盤方格試驗中,剝離數為3〜J 〇個; X ·· 1 0 0個棋盤方格試驗中,剝離數為丨丨個以上,· 〔實施例2〜7〕 在實施例2〜7中,如表i所示,除改變構成車輛 表板基體材料之難黏合性基體材料種類及對於車二義 儀表板基體材料之矽氧化焰處理時間外,餘與實施例^/ 法分別進行車輛用前部儀表板基體材料及立體裝同 估。 、τ 1千之評91082NKTISMJP-F0l6TW.ptd Page 27 1225873 V. Description of the invention (25) 2 · Evaluation of difficult-to-adhesive base materials Use standard solution 'to measure the wet bleaching of the base material of the front instrument panel of the vehicle after the silicon oxide flame treatment has been performed index. The same method was used to measure the wetness index of the base material for the front instrument panel of the vehicle before the silica flame treatment. 3 · Evaluation of three-dimensional decorative parts For the front instrument panel of a vehicle obtained by forming a foamed urethane layer and a decorative member on the base material of the front instrument panel of a vehicle, the decoration is measured in accordance with the checkerboard test (JIS standard). The peel strength of the component is evaluated on a benchmark basis. ◎: No peeling in 100 checkerboard test; ○: 2 peeling in 100 checkerboard test; △: 3 ~ 100 in 100 checkerboard test J 〇; X ·· 100 checkerboard test, the number of peeling is 丨 丨 or more, [Examples 2 to 7] In Examples 2 to 7, as shown in Table i, except for changing the composition Except for the types of difficult-to-adhesive base materials for the base material of the vehicle panel and the silicon oxide flame treatment time for the base material of the vehicle ’s instrument panel, the rest is the same as that of the embodiment ^ / estimate. , Τ 1 thousand reviews
91082NKTISMJP-F016TW.ptd 第28頁 1225873 五、發明說明(26) 〔比較例1〕 除採用由不含矽烷化合物之壓縮空氣及丙烷組成的燃 燒氣體,取代實施例1中含有矽烷化合物之混合氣體外, 餘以與實施例1同法分別進行車輛用前部儀表板基體材料 及立體裝飾件之評估。 表 191082NKTISMJP-F016TW.ptd Page 28 1225873 V. Explanation of the Invention (26) [Comparative Example 1] Except that a combustion gas composed of compressed air and propane containing no silane compound is used instead of the mixed gas containing the silane compound in Example 1 In the same way as in Example 1, the evaluation of the base material and three-dimensional decorative parts of the front instrument panel for vehicles was performed separately. Table 1
難黏合性 基體材料 改質處理 (秒) 濕濡指數(dyn/cm) 棋盤方格試驗 處理前 處理後 處理前 處理後 實施 例1 PP 30 34 68 X ◎ 實施 例2 PP 60 34 69 X 〇 實施 例3 PE 30 32 66 X ◎ 實施 例4 PE 60 • 32 68 X ◎ 實施 例5 PET 30 38 68 X ◎ 實施 例6 PET 60 38 70 X ◎ 實施 例7 氟乙烯樹脂 60 31 65 X ◎ ‘ 比較 例1 PP 30 34 36 X XModification treatment of difficult-to-adhesive base materials (seconds) Wet index (dyn / cm) Checkerboard test Pre-treatment Post-treatment After pre-treatment Example 1 PP 30 34 68 X ◎ Example 2 PP 60 34 69 X 〇 Implementation Example 3 PE 30 32 66 X ◎ Example 4 PE 60 • 32 68 X ◎ Example 5 PET 30 38 68 X ◎ Example 6 PET 60 38 70 X ◎ Example 7 Fluoroethylene resin 60 31 65 X ◎ 'Comparative Example 1 PP 30 34 36 XX
91082NKTISMJP-F016TW.ptd 第29頁 1225873 五、發明說明(27)91082NKTISMJP-F016TW.ptd Page 29 1225873 V. Description of Invention (27)
產業上夕可剎用性 如上所述,若採用本發明之立體裝飾件 時,藉由斜經予立轉^ 八表k方法 ^错由對心=立體加工的難黏合性基體材料表面及 層表面或任一者之表面,施以;ό ^ &人& 曰 的火焰處理,料在不實施合物之燃燒氣體 具施特殊的塗底處理而藉由中間 =;?力二的難黏合性基體材料及裝飾構件之間獲得 牛固的接著強度。 Φ 此外,若採用本發明之立體裝飾件製造方法時,藉由 j予立體加工的難黏合性基體材料表面及中間層表面或 者之表面’細*以源自含石夕烧化合物之燃燒氣體的火焰 =理、’即可在不實施特殊的塗底處理而藉由中間層,高效 二且迅速的提供經予立體加工的難黏合性基體材料及裝飾 構件間具有牢固接著強度之立體裝飾件。Industrial availability is as described above. When the three-dimensional decorative part of the present invention is used, the oblique warp is used to make a vertical turn ^ The eight-table k method ^ Wrong and right = The surface and layer of the hard-to-adhesive base material processed three-dimensionally The surface or any one of the surfaces is subjected to a flame treatment, which means that the material is not subjected to a special primer treatment without the combustion gas of the compound, and the middle is difficult. Adhesive bonding strength is obtained between the adhesive base material and the decorative member. Φ In addition, if the three-dimensional decorative part manufacturing method of the present invention is used, the surface of the hard-to-adhesive base material and the surface of the intermediate layer or the surface of the three-dimensionally processed by j is 'fine *' Flame = reason, 'You can quickly and efficiently provide three-dimensional decorative parts with solid bonding strength between the hard-to-adhesive base materials and decorative components through three-dimensional processing through the intermediate layer without performing a special primer treatment.
1225873 圖式簡單說明 【圖式簡單說明】 第1圖係為用於說明本發明第1實施形態相關的立體裝飾 件的第圖。 第2圖係前部儀表板斜視圖。 第3圖係車門斜視圖。 第4圖係座椅斜視圖。 第5圖係操作箱斜視圖。 第6圖係裝於車門上的内裝材料斜視圖。 第7圖係保險桿斜視圖。 第8圖係車輛裝飾品斜視圖。 1 第9圖係用於說明本發明有關的立體裝飾件之製造方法 圖。 第1 0圖係用於說明表面改質裝置構造圖。 第11圖係用於說明火焰喷吹方法圖(之一)。 第1 2圖係用於說明火焰喷吹方法圖(之二)。 第1 3圖係用於說明火焰喷吹方法圖(之三)。 第1 4圖係用於說明表面改質裝置火焰喷吹方法圖。 第1 5圖係用於說明攜帶型表面改質裝置圖。 第1 6圖係用於說明裝飾構件粉末空殼成形方法圖(之 一)。 第1 7圖係用於說明裝飾構件粉末空殼成形方法圖(之 二)。 第1 8圖係用於說明裝飾構件層合方法圖(之一)。 第1 9圖係用於說明裝飾構件層合方法圖(之二)。1225873 Brief description of the drawings [Simplified description of the drawings] Fig. 1 is a diagram for explaining a three-dimensional decorative piece according to the first embodiment of the present invention. Figure 2 is an oblique view of the front instrument panel. Figure 3 is a perspective view of the door. Figure 4 is a perspective view of the seat. Figure 5 is a perspective view of the operation box. Fig. 6 is a perspective view of the interior material mounted on the door. Figure 7 is a perspective view of a bumper. Fig. 8 is a perspective view of a vehicle ornament. 1 FIG. 9 is a diagram for explaining a method of manufacturing a three-dimensional decorative piece according to the present invention. Fig. 10 is a structural diagram for explaining a surface modification device. FIG. 11 is a diagram (one) for explaining a flame blowing method. Figure 12 is a diagram (No. 2) for explaining the flame blowing method. Figure 13 is a diagram (No. 3) for explaining the flame blowing method. Figure 14 is a diagram for explaining the flame blowing method of the surface modification device. Figure 15 is a diagram illustrating a portable surface modification device. Fig. 16 is a diagram (No. 1) for explaining a method for forming a powdery shell of a decorative member. Fig. 17 is a diagram (No. 2) for explaining a method for forming a powdery shell of a decorative member. Fig. 18 is a diagram for explaining a method of laminating a decorative member (part 1). Figure 19 is a diagram for explaining the method of laminating decorative components (No. 2).
91082NKTISMJP-F016TW.ptd 第31頁 1225873 圖式簡單說明 【圖號說明】 ίο 難黏合性基體材料表面改質裝置 12 貯罐 14 矽烷化合物 16 加熱手段 18 壓力計(或係液面水平計) 22 混合室 24 輸送部 28 壓,力計 3 2 喷射部(燃氣器) 34 燃料氣體火焰 3 6 旋轉檯 38 固定夾具 42 黏合性基體材料表面改質裝置 4 4 箱子 46 筒式貯罐 4 7 配管管件 50 立體裝飾件 54 裝飾構件 56 中間層 57 中間層 58 難黏合性基體材料91082NKTISMJP-F016TW.ptd Page 31 1225873 Brief description of drawings [Illustration of drawing number] ίο Surface modification device for difficult-to-adhesive base material 12 Storage tank 14 Silane compound 16 Heating means 18 Pressure gauge (or liquid level meter) 22 Mixing Chamber 24 Conveying section 28 Pressure and force meter 3 2 Injection section (gas burner) 34 Fuel gas flame 3 6 Rotary table 38 Fixing fixture 42 Adhesive base material surface modification device 4 4 Box 46 Cartridge tank 4 7 Piping pipe fittings 50 Three-dimensional decorative parts 54 Decorative members 56 Intermediate layer 57 Intermediate layer 58 Hard-to-adhesive base material
91082NKTISMJP.F016TW.ptd 第32頁 1225873 圖式簡單說明 64 喷射口 82 金屬製空殼金屬模 84 成形模 85 成形面 8 6 加熱裝置, 88 備用罐 92 粉末樹脂 98 冷卻手段 101 前部儀表板 102 車,門 103 座椅 104 操作箱 105 内裝材料 106 保險桿 107 裝飾品91082NKTISMJP.F016TW.ptd Page 32 1225873 Simple description of the drawing 64 Jet port 82 Metal shell mold 84 Molding mold 85 Molding surface 8 6 Heating device, 88 Spare tank 92 Powder resin 98 Cooling means 101 Front instrument panel 102 Car Door 103 seat 104 operation box 105 interior material 106 bumper 107 decoration
91082NKTISMJP-F016TW.ptd 第33頁91082NKTISMJP-F016TW.ptd Page 33
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