TW315384B - - Google Patents
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- TW315384B TW315384B TW083110816A TW83110816A TW315384B TW 315384 B TW315384 B TW 315384B TW 083110816 A TW083110816 A TW 083110816A TW 83110816 A TW83110816 A TW 83110816A TW 315384 B TW315384 B TW 315384B
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- Taiwan
- Prior art keywords
- compound
- atoms
- silicon
- general formula
- item
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/76—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing silicon
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
- B29C33/60—Releasing, lubricating or separating agents
- B29C33/62—Releasing, lubricating or separating agents based on polymers or oligomers
- B29C33/64—Silicone
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/50—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen
- C10M105/54—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen containing carbon, hydrogen, halogen and oxygen
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/38—Lubricating compositions characterised by the base-material being a macromolecular compound containing halogen
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- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/50—Lubricating compositions characterised by the base-material being a macromolecular compound containing silicon
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/003—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions used as base material
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/0406—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen used as base material
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- C10M2211/0425—Alcohols; Ethers; Aldehydes; Ketones used as base material
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- C10M2211/044—Acids; Salts or esters thereof
- C10M2211/0445—Acids; Salts or esters thereof used as base material
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- C10M2211/06—Perfluorinated compounds
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- C10M2213/00—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2213/02—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen and halogen only
- C10M2213/023—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen and halogen only used as base material
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- C10M2213/04—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen
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- C10M2213/04—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen
- C10M2213/043—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen used as base material
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- C10M2213/0606—Perfluoro polymers used as base material
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- C10M2213/062—Polytetrafluoroethylene [PTFE]
- C10M2213/0623—Polytetrafluoroethylene [PTFE] used as base material
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- C10M2227/02—Esters of silicic acids
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- C10M2229/02—Unspecified siloxanes; Silicones
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- Cosmetics (AREA)
Description
A7 B7 315384 五、發明説明(1) ^^1- ^^^1 ^^^1 II ^^^1 In R ^^^1 ^ϋ_· i^n ei^i 、 穿 t (請先閲讀背面之注$項再填寫本頁) 本發明傜有關於離.棋劑,由該離模劑所得之硬化皮膜 以及使用該離模劑之成形方法,詳而言之傺有關於在製造 由合成樹脂或橡膠等的离分子化合物所形之成形品時所使 用之離棋爾,硬化皮膜及成形方法。 要製得由樹脂或橡膠所構成之成形品時乃將樹脂或橡 膠材料先充填在模具之中來成形,通常在充填前先用離模 劑塗佈棋具。 通常將石嫌、聚乙烯嫌等蠟類,聚二甲基矽氣烷二醇 、矽樹脂類之矽酮,乙二醇、脂肪酸衍生物,含有全氟烷 基之化合物之類的有機化合物,礦油、滑石、雲母等無機 化合物分散成滲於水或有機溶劑來成為離模劑。 經濟部中央標準局貝工消費合作社印製 埴些離棋劑,通常必需塗佈使用,在作業上為了使步 驟次數減少,故希望能開發出壽命較長之離模劑。再者, 每次塗佈後離模劑堆積造成模具之污染問題,特別是石蠟 糸的離模劑污染的程度联重。此外,由於必需毎次塗佈, 基本上會有離模剤粘至成形品上之情事,此會造成成形品 粘在一齊等的後處理不良問題,而形成後段加工步驟成形 品之塗裝不良及接著不良等的原因。特別是當使用矽酮糸 的離模劑時容易造成塗裝不良或接箸不良之原因。 此外,要成形聚氨基甲酸酯發泡體之成形品時,有成 形品之表面氣泡會變粗大之缺點。此種情形特別是在使用 矽_油作為離模劑時更為顯著。 為了解決這些缺點,有各種的離模劑被開發出來。例 如含有4〜20個硪原子之全氟烷基之磷酸酯或其鹽與矽_ -4 - 本紙張尺度適用中國國家橾準(CNS ) A4規格(210X297公釐) ^15384 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) 油之混合物(日本特公昭53-23270號,53-23271號公報),含 有4〜20個硪原子之全氟烷基之磷酸酯或其鹽與矽酮清漆 之混合物(日本特公昭57-48035號公報),含有全氟烷基之 聚醚化合物與矽銅油等之混合物(日本特公昭59-32513號公 報)。逭些離模劑為離模性能優良之離棋劑而且離模壽命 亦較以往者為長。而且,由含有全氟烷基之聚醚化合物與 矽詷油等的混合物所構成離模劑亦幾乎不影響大部份的高 分子化合物成形品之二次加工性。但是這些離模劑仍不能 滿足隨著高分子化合物成形品之形狀的後雜化及大型化所 要求之離模性能及離模赛命。 此外,日本特公平3-39804號公報中掲示了一種包含具 有全银院基之丙嫌酸糸聚合體及有機silsesquioxane的無規聚 合體的離模劑來作為延長離模壽命之形成硬化皮膜型離模 劑。此種離棋劑初期的離模性能優良;離模壽命雖可作某 些程度之延長;但由於硬化皮膜之強度不足故仍不能得到 令人滿意之離模赛命。 再者,日本特公平3-226Θ5號公報,掲示了一種含有聚 二甲基矽氣烷及由下式: (Z^) uS i Z24-« (其中Z1為甲基、乙基、丙基或甲氣乙基,Z2為硪原 子數1〜4之1價烴基或鹵化烴基,u為3或4之整數) 所示之烷氣二矽烷或其部份水解及縮合而生成之寡聚物生 成物以及四烷基鈦酸鹽等的金屬醇鹽的離模劑。但是,此 種離模劑之離模赛命或二次加工性仍不夠令人滿意。 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再填寫本頁) 訂 315384 A7 B7五、發明説明(3) 本發明鑑於前逑之問題點,目的乃是要得到一種離模 性能優良,離模赛命長而且成形品之表面加工性亦良好且 不會影《成形品的塗裝或接著等二次加工性之離模剤。 本發明乃是有两於由通式(I)表示之含有矽之化合物 (A): R^S i R24-〔式子中R1為 R3 (I) 0 K' r3 ” _C_R3 -〇-C = CH2 = ^ N -N-C-R4n-NH-<^) 0 R4 經濟部中央揉準局員工消費合作社印裝 (R3、R4分別為«原子數為1〜4之«基,R2為硪原子數 為1〜4之烴基或鹵化烴基,η為3或4之整收〕)及 (B)l分子内含有羥基或烷氣基二値以上之含矽及/或 氟之化合物所構成之離模剤;該離棋剤所得到之硬化皮膜 以及使用該離模剤之成形方法。 本發明所使用之通式(I)之含有矽之化合物(Α): RinS ί R24-n (I) 中R1雖為 R3 〇 R3ii „ I O-C-R3 -0-C = CH2 r3 j -0 -N = > -N-C-R4n-NH-<^)、 \r4 IIR 0 等基画,從反應性、非腐蝕性及原料是否易於取得等 . 3 方面來看,以一 0 — N = C:^=4j為最佳(其中R3、R4分 別為硪原子數1〜4之i基)。具體而言為甲基、乙基、+ 本紙張尺度適用中國國家標準(CfJS ) A4規格(21〇X 297公羡) ϋ—i ^^^1 Ha.· ^^1« immt I -c^ ^^^1 ^^^1 ^^^1 Mmml ^^^1 ^^^1 - ^ 一 穿 i (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局貝工消費合作社印製 A7 B7 五、發明説明(4 ) 丙基、丁基、異丙基、異丁基、特一 丁基等。從反應性來 看,R3、R4分別為甲基、乙基者為佳。此外,R3和R4組合 時,從反應性觀之其中有一為甲基或乙基者為佳。R2為硪 原子數1〜4之烴基或鹵化烴基。烴基例如甲基、乙基、 丙基、丁基、異丙基、異丁基、待一 丁基等。鹵化烴基例 如三氣丙基、三氯乙基等。這些當中從離模性及反醮性觀 之以硪原子數為1〜2傾之烴基為佳。η為3或4之整數 。萨為1値或不存在。 前述通式(I)所表示之化合物(Α)例如可為通式(I)所 表示之化合物: R^S i R24-n (Π) ___ ϋ3 〔式子中R1為 _ 〇 — Ν = C = ( R3、R4分別為硪 原子數1〜4之烴基,R2為硪原子數1〜4之烴基或鹵化 烴基,η為3或4之整數)〕 亦即,含有矽之化合物(Α)之具體例子如下: _ — - ·-0 0 〇 II II ||
Si(0-C_CH3)4、Si(0-0-CH2CH3)4、Si(0~0-iCH2CH2CH3)4、 0-0 〇 II II II CH3Si(0-C-CH3)3、CH3SK〇-C-CH2CH3)3、CH3CH2Si(OCCH3)3、 〇 Ο
II II CH3CH2Si(0-CCH2CH3)3、CF3CH2CH2Si(0-C-CH3)3 等的脱羧酸型, CH3 CH2CH3 CH9 I I I 3
Si(0-C=CH2)4、Si(0-C = CH2)4、CH3Si(0_C = CH2)3 ' CH2CH3 CH3 CH3Si(0_C = CH2)3、CH3CH2Sii:0-C = CH2)3、 ch3 .等的脱酮型, 本紙張尺度適用中國國家揉準(CNS ) A4規格(210X297公釐) i i ^^^1 t—^1 I ^^^1 emmmmmme *1 ^i ~ (請先閲讀背面之注意事項再填寫本頁) 315384 A7 B7 五、發明説明( CH3 ch3 ch3
Si(N-C-CH3)4、CH3Si(N-C-CH3)3、CH3Si’(N-Jj-CH2CH3)3 0 0 〇 CH3 ch3 CH3CH2Si(N _C -CH3)3、CF3CH2CH2Si(N-丨? -CH3)3 · 0 〇 等的脱醛按型,
Si(NH-<^))4 . CH3Si(NH-^^)3, CH3CH2Si(NH-^))3 等的脱胺型,
S
Si (〇NCch3、
Si(〇NC<CH23CH2CH2CH3^-C、呵以⑽叭心、CAS"·、:,、 CF3CH2CH2Si C〇NC<^32CH3)3n CH3 CH2 CH2 CH2- Si(ONC<^3 ^^1- ^—>1 if m m It— HI I m In n (請先閲讀背面之注^項再填寫本頁) 經濟部中央樣準局員工消費合作社印製 CH2CH2CH3'3、 CCI3CH 2CH2Si(ONC〈 CH3
CH3 SiCONC ch3 ch2ch3;3 )3 CH3 c H3 等的脱肟(oxime)型 本紙張尺度適用中國國家標準< CNS ) Λ4規格(210X297公釐) 2 X 10-II • 1 R — S — R ik ο I 9 i 3 R丨S丨X It ο
(V A7 B7 五、發明説明(6 ) 前述含有矽之化合物⑷具有使下列所述之含有矽及/ 或氟之化合物交聯之作用。 一分子内含有二值以上之羥基或烷氣基之含有矽及/ 或氟之化合物⑻列舉如下: 例如最好為具有下面通式(V)之化合物: R5 r7
1 1 I X - S i - 0 i R6 R8 〔式子中j為正整數、k為0或正整數、j + k的平 均為10以上、最好為20〜5000之數、X1、X2為-OH、~0R12、 -R13NH2 、 - R14〇H 、 -R15C00H 、 -R13SH 或-R12 、 X3 為-OH 、 -OR12 、 -R13Nfe、-R1%!!、-R18C00H、或-R15SH (但是 k 為 0 時X1、X2均 為-OH或-OR12 , k不為0時X1、X2之至少二値為~0H或~0R12、 R12為碩原子數1〜4之烷基、鹵化烷基或苯基,R13為硪原 子數1〜10之烯基(alkylene)或RieNHCH2CH2 - (R16為硪原子數1 〜4之烯基、為 -(CH2 ch2 0^(chch2 0^CH2^c η -<〇)^ch2>5 ch3 (但是a為0或1〜:15之整數、b為0或1〜15之整 數、c為1〜10之整數、d為1〜5之整數(ϋ18為硪原子 數 1 〜10 之烯基),!?5、Re、R7、Re、Re、R10、R11 為硪原 芋數1〜4之烷基,鹵化烷基或苯基〕。 此外 _ 9 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 1^1 ^^^1 n 11 (ϋ ^—>1· ^1· eea— (請先閎讀背面之注$項再填寫本頁) 經濟部中央標準局員工消费合作社印裝 315384 A7 B7 五、發明説明(7) R7 R9
I I —(Si - 0)—和一fSi - 0>- k ^ , 為成無規或嵌段式結合。
Rs、Re、RT、Re、Re、Rie、R11、R12 之具釀例子為甲基 、乙基、丙基、異丙基、丁基、異丁基、特一丁基等的烷 基、三氣乙基、三氟丙基、三氯丙基等的鹵化烷基、苯基 等。從反應性及離模性來看以甲基、乙基、三氟丙基為佳 R13之具體例子為: -CH2 -、4CH2 兮、4CH21、_(CH2 打、 - C Η 2 C Η _、C Η 2 C H ch3 ch3 等的烯基及-CHaCfeNHCHaCfc-、~CH2CH2ClteNHCH2CH2-,而從這 些的反應性及離模性來看以-(Cfc)2-、-(CH2)3-、-(〇teU-為佳。 R14之具體例子為: 4CH2h、~(CH2·^·、、-(CH2々〇、 經濟部中央標準局貝工消费合作社印製 (請先閲讀背面之注意事項再填寫本頁) ~^(〇)~ ch2ch2ch2-、-ch2ch2och2ch2ch2-、 -4CH2 CH2 O^j-g ch2 ch2 ch2- ^ -4CHCH2 o^-ch2 ch2 ch2- ch3 而從反騾性及離模性來看以-(CH2)2-、-(CH2)3-、、 -CHaCHaOOteCHaCHs-為佳。 R15之具體例子為 _(CH2)2-、-(ch2)3-、-(CH2>4、-(CH2)S-、 • 10- 本紙張尺度適用中國國家梯率(CNS ) A4规格(2丨0X2.97公釐) 經濟部中央標準局員工消費合作社印裝 A7 ___^__B7_ 五、發明説明(8 ) -(CH:〇10-,而從反應性及離模性來看以》(CH2)2-、-(Clfe)3-、 等為佳。 X1、X2 之具醱例子為:-OH、-0CH3、-OCHzCHa、-OCH2CH2CH3 、-CH2CH2CH2冊2 、 -CHaCHzCHzOH 、 -CH2CH2CH2OCH2CH2OH 、 -(CH2)ie-C00H 、 -CHaCIteCIfeSH、~CH3、·〇Η2〇13而從反應性及離棋性來看以~0H、 OClb、~(〇2〇|3、^OCHsCHisCIfe 為佳。 X3 之具釀例子為:~0H、~(〇3、"OCHaCHa、-OCHaCHzCfe、 -ClfeCMzNIte、-OfeCHzCHzOH、-CH2CH2CH2OCH2CH2OH、-(CHsOie-COOH、 -CH2CH2CH2SH,而這些當中從反應性及離模性來看以.、 0CH3、~〇〇|2〇|3、~〇CH2CH2CH3 為佳。 j從反應性、雔模性來看以為10〜5800以整數為佳。 k從反應性、離模性來看以0〜500之整數為佳。 通式(V)所表示之化合物使用j與k總和不同者為佳 ,j和k之總和需在10以上,而從反應性及離模性之觀點 來看以為2Θ〜5000之整數為佳。 a從反應性及離模性來看以為從0〜15之整數為佳。 b從反應性及離模性來看以為從0〜15之整數為佳。 c從反應性及離模性來看以為從1〜10之整數為佳。 通式(V)所示之化合物具體之例子為: CH3
I
HO -iSi - 〇^-H I :- CH3 (P平均為20〜5000)、 ch3
I
CH3O -iSi - 0>p CHg I CH3 (p平均為20〜5000)、 本紙張纽適用中國國家標準⑽⑴视^⑽謂公釐)-11- ^^1- eimmmt 11 ^^^1 ^^^1 ^^^1 ^ memeMe ^^^1 ^^^1 m n 1·、一s4 (請先閲讀背面之注意事項再填寫本頁) 五、發明説明(9) A7 B7 ch3 ch3 ch3 ch〇I · I I I HO — Si0-(Si0i0i - OH CH3 CH3 OCH3' CHo ( J+k平均為20〜5000)、 ch3 ch3 ch3 ch3 I I I I CHgO — SiO-^SiO(Si0^vSi — 0H I I J I I CH3 C H3 0CH3 CH3 ( j+k平均為20〜5000)、 ch3 ch3 ch3 ch3I I I I HO - SiO^SiO^j-fSiO^Si - OH I ' I ch3 ( j + k平均為2卜5000) CH2CH2CH2NH2 f ch3 ch3 ch3 ch3 ch3 ch3I I I I HO - SiO-^SiO^j-eSiO^Si - OH C H3 C H3 I C H3 ( j + k平均為20〜5000)、 ch2ch2ch2sh (請先閲讀背面之注$項再填寫本頁) Γ 經濟部中央標準局貝工消費合作社印製 CH3 CH3 ch〇 ch3 I I I I CH3- SiO-iSiO^SiO^Si - CH3 CH3 CH3 OH CH3 ( j+k平均為20〜5000、k為2以上)、 CH3 CH3 CH3 CHoII II , CH3- SiO-(SiO)j^SiC^kSi - ch3 CH3 CH3 och3 0h3 ( j 午k平均為20〜5000、k為2以上)、 -12- 本紙張尺度逍用中國國家揉準(CNS)A4規格(210x297公釐) 315384 Α7 Β7 經濟部中央標準局員工消費合作社印装 五、發明説明(10) ch3 ch3 ch3 ch3I I I I CH3- Si0-(Si0^j-fSiO^Si - CH3 ch3 ch3 CHg U + k平均為20〜5000、k為2以上)、
CH2CH2CH2OH ch3 ch3 ch3
HO - CH2CH20CH2CH2CH2Si0-f SiO ^-SiCH2CH2CH2OCH2CH2〇H ch3 ch3 ch3 (P平均為20-5000) 〇 前述通式(V)所表示之化合物中以通式(VI): R5I X4 〇-<Si - 0)m- X5 (礓) R6 C式子中Rs、浐分別為硪原子數1〜4之烷基或鹵化烴基 或苯基、X4、X5分別為氫原子或硪原子數1〜4之烴基、 m為平均10以上,最好20〜500Θ之整數〕所表示之化合物 為佳。 R5、Re具髖言之為甲基 、異丁基、特一丁基等烴基 乙基、三氣丙基等鹵化烴基 觀之,以甲基、乙基、三氟乙基、三氧丙基為佳。 X4、XS之具體例子為·· H、CHn、CFUCH C H 〇C H 2C Η 3^ --/CH3 乙基、丙基、丁基、異丙基 三氣乙基、三»丙基、二氟 逭些當中從反應性及離模性 3 ch^ch^ ch2ch2ch2ch3 這些當中從反應性來看以H、CH3為佳。 通式(υι)所示之化合物以混合以不同者來使用為佳, -13- 本纸張尺度逋用中國國家標準(CNS ) Α4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁)
經濟部中央標準局貝工消費合作社印製 A7 B7 五、發明説明(11 ) m平均10以上,從反應性、離棋性來看,以20〜5000為佳 ,20〜3000更佳,20〜2000最佳。 通式(V)所示之化合物之具醭例子為: CH3
I HO(Si - 0^- Η CH3 (P平均為20〜5000)、 ch3
CH30(Si - CH-p H
I CH3 (P平均為20〜2000)、 CH3
I CH3CH2〇(Si - 〇VCH3 ch3 (P平均為20〜2000)、 9
H0(Si - 〇^p-H (P平均為20〜2000)、
ch2ch2cf3 I
H0(Si - O^p-H 、ch2ch2cf3 (p平均為20〜細)、 另外的例子為: Y1OCH2Rie〇-Rie_Ri7CH2〇y2 (VI) 所表示之化合物,〔式子中Y1、^分別為氳原子或硪原子 數 1 〜4 之烴基,Rie為:一 CF2、_CF2CF2 — cf3 -CF - 、R17 為一 CF2 —、一 CF2CF2_ 或 -14- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)
3 - F F ^ CIC HI· m_* ^^^1 ^^i·· ·ϋι ϋ·— I 11 ^^^1 ^^^1 i···— (請先聞讀背面之注意事項再填寫本頁) CF3 A7 B7 五、發明説明(12) 卜 —r1 π 為由2 s2 為由 s擔造單位之至少1種, 所組成之族中選出之0
Rie為 CF3 或 _CF2 CF2 CF_ I — CFCF2 一 -CF2CF- ' cv ee丨、丨上,最好是10〜200 ) ° S1 +萨+ s3苹均5以上 -诚1)18¾抱聚合物*無規共聚物,嵌段共聚物 此外,抑进1 K ^ ,或交互共聚物均可。 γ1、户之具鳢例子為S原子、甲基、^基、丙基、異 仗逛戸®當中,從反ϋ性來看以子、甲基 丙基、丁基寺。3^ — 為佳。 通式(VI)所示之化合物混合S1 + S2 + S3不同者來使用 較佳 Sl + S2 + S3平均済為5以上,從反應性來看最好10 〜200,.較好是〜100 ,更好是I®〜明。 再者,通式(VI)所示之化合物較佳之例子為:
HOCH2(CF2 〇)1〇 (CF2 CF2〇)i2 CF2 CH2〇H
HOCH2CF2CF20 (0¾ CF2 CF2 O)i〇 CF2 CF20 (CF2CF2 CF2 O)10CF2CF2CH2〇H
CH3OCH2 CF2 CF2 0 (CF2 CF2 CF20)2〇 cf2 cf2 o (cf2 cf2 cf2 o)2〇cf2cf2 CH2〇H cf3 cf3 CF3 cf3
hoch2 CFO (CF2 cf〇)15 cf2 cf2o (CFCF2〇)15CFCH2〇H o 另外的例子為通式(VI):
RfAlSi (〇A2)s6A33_s6 ⑽ -15- ,: 本紙張尺度逋用中國國家標準(CNS ) A4規格(210X297公釐) HI n ^^^1 I ^i··· ^^^1、一 (請先閲讀背面之注意事項再填寫本f) 經濟部中央樣準局貝工消費合作社印装 315384 A7 B7 五、發明説明() 所表示之化合物,(式子中Rf為硪原子數6〜21之全氟烷 基,A1為硪原子數,2〜6之烯基,A2為氫原子或硪原子 數1〜4之烷基,A3為硪原子數1〜4之烷基,SeS2或 3)〇 之具醱例子為: C F (C F 2) 了、C F 3 ( C F 2) 9、C F : (C F 2) 13、C F 3 ( C F 2) 15、C F “ CF3、
(C F 2) 5" C F (C F2) 11' C F (C F2> 17' C F (C F ,) 2J 19 >CF(CF2)4 CF3 cf3< ,CF(CF2)6 cf3 cf3' >CF(CF2)8 nl> ^^^1 ^^^1 nn n^i n^i —an ι_·ϋ ·ϋ_1¾.τ (請先閲讀背面之注意事項再填寫本頁) cf3 cf3n CF3y CF3< CF(CF2)i〇 >cf(cf2)12 經濟部中央標準局貝工消費合作社印装 cf3 cf3. cf3 cf3. cf3 cf3> cf3v 心灯2)14 ^CF(CF2)i6 -CF(CF2)i8 16- 本紙張X度適用中國國家揉準(CNS > A4«L格(210X297公釐) H 9C H 〇C Η -ch3、- ch2ch3、 3、-ch〈工、-ch2ch2ch2ch3 A7 ___B7_ 五、發明説明(14 ) 這些當中,從離模性來看以CF3(CF2)7、CF3(CF2)e、、 CF3(CFa)i3 等為佳 β Α1之具醴例子為:一^ ττ ^ h2c h2-n - c h2c ch3 ' -CH2CH - 、— ( C H 2) 6_ ,而從離模性來看, 以"CHaCIfe-為佳。 A2之具體例子為氫原子, ,而從反應性來看以氬原子,~CH3, CH2CH3為佳。 f A3之具體例子為甲基、乙基、丙基、丁基、異丙基、 異丁基等*從反應性來看以甲基或乙基為佳。
SeM反應性來看以3為佳。 另外的例子為包含通式(II):
RfA4A5 〔式子中Rf與前面相同,A4為碩原子數1〜6之烯基,A5 % 0 CH« 0
^ II I d II 0 - C - C = CH2 或 o-cch = ch2 !11—— 1!·^— I— ^ n n n in ϋ (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局貝工消費合作社印装 所表示之化合物20 % (重量% ;以下相同)與通式(IV): Ae0A7A8 (式子中八8為氫原子或硪原子數1〜4之烴基;A為硪原 Η份 one -物 ο合 聚 共 為 2作 為 Η上/3ac ,C1C -殳 基 I 2 稀o=c物 之一合 6 ο化 ^ 之 1 示 數表 子 所 或 ch2 ) 且數量平均 -17- 本紙張尺度適用中國國家揉準(CNS ) A4規格(2丨0><297公釐) A7 B7 五、發明説明(15 ) ^ 分子量為1000以上之共聚合體,從離模性來看以數悬平均 分子量為30Θ0以上者為佳。
Rf如前述。 A4之具體例子為: -ch2ch2ch2ch2- ch3 I -CH2CH - 、- ( C Η 2) -C Η 、-C HgC a 2~ ,從離棋性來看以 經濟部中央標準局貝工消費合作社印装 -CH2-、CHaCfe-為隹 β 通式(1)所示之化合物具釅之例子為: CH2= Cli—C02CH2CH2(CF2)7 CF3、 CH2=CC02CH2(CF2)9 CF3、 ch3 CH2 = CHC〇2(CH2)6 (CF2)i5CF3、 CH〇 I ° Q p CH2= CHC02CCH2(CF2 )8 CF< 3、 CF3 CH I C F ch2 = cco2ch2ch2(cf2 )16cf< 3、 cf3 CH2=CHC02CH2CH2(CF2)4 cf3 Ae之具體例子為氣原子,甲基、乙基、丙基、丁基、 異丙基、異丁基等,從反鼴性來看以氫原子、甲基為佳。 A7之具體例子為:_CH2~、一 CH2CH2_ 一 (C Η 2) 6- ch3 i chch2 18- 本紙張A度適用中國國家標準(CNS ) A4W ( 210X297公瘦) HI nn *^^1 In HI —1 ϋι« I ^^^1 ^^^1 m IK nn n^i、一seJ (請先閲讀背面之注$項再填寫本頁) A7 B7 315384 五、發明説明(16 ) 通式(IV)所示之化合物之具醱例子為: CH2 = CHC〇2 CH2 CH2 OH、C Η 2 = C H C 0 2 C H 2 C Η 2 C Η 2 Ο Η、 CH3 ch3 (請先閲讀背面之注$項再填寫本頁)
I I CH2= CC〇2(CH2)6 〇H 、CH2 = CC02 CH2CH2〇H、 CH〇 I 3 CH2=CHC02CHCH2〇CH3 Λ CH2=CHC〇2CH2CH2OCH2CH3 λ CH2 = CHC〇2CH2〇CH2 CH2 CH2~CH3 共聚合體中需包含通式(Π )所表示之化合物20 %以上 ,從離棋性來看較好包含40%以上,最好88%以上,上限 為98%〇如果在20%以下具有離模性不良之傾向。 通式(IV)所示之化合物在共聚合體中含有2%以上, 從反應性之觀點之最好含有3%以上,較好是5%以上, 最好不超過20%之上限。如果較2%為少會有反應性變壤 之傾向。 經濟部中央標準局貝工消費合作社印製 前述共聚合髏之共聚合成份除了可為通式(I)、(IV) 之化合物以外,亦可使用乙烯、丙烯、氛乙烯、鴒二氣乙 烯、醋酸乙烯酯、丁基乙烯酯及甲基丙烯酸甲酯、甲基丙 烯酸酯、丙烯酸月桂酯、丙烯酸硬脂醯酯、丙烯酸2-乙基 己基丙烯酸酯、甲基丙烯酸缩水甘油酯等丙烯酸酯。而從 離楔性來觀之,以丙烯酸月桂酯,2-乙基己基丙烯酸酯等 的高级醇的丙烯酸酯類較好用。 含有矽及/或氟之化合物(含有通式(M)所示之化合 -19- i. 本紙張尺度適用中國國家揉準(CNS ) A4規格(210X297公嫠) A7 B7 經濟部中央樣準局員工消費合作社印製 五、發明説明(Γ7 ) 物及通式(IV)所示之化合物作為共聚合成份之共聚體,通 式(V)、通式(VH)或通式(VI)所示之化合物)之一分子内 具有羥基或烷氣基二個以上,故交聯反應性,可得到離模 性優良之硬化皮膜。 前面所列舉之6種含有矽及/或氟之化合物可以分別 單獨或組合使用;將不同種類者組合超來使用亦可。 對本發明之離棋雨賦予離模性之化合物乃是前述之含 有矽及/或氟之化合物(含有通式U)所示之化合物及通 式(IV)所示之化合物作為共聚合成份之共聚體,通式(V) 、通式(Vi)或通式(通)所示之化合物)。 本發明之離模剤除了合有前述之含有矽之化合物(A)及 合有矽及/或氟化合物⑻以外,亦可依需要含有硬化促進 劑、溶劑等。 硬化促進劑乃是在含有矽之化合物(A)和含有矽及/或 氟化合物不反應或反應理緩時適當添加之。硬化促進薄(之 例子如四烷基鈦酸酯,四烷基亞鍺酸酯、四烷基結酸酯、 釩三酵鹽等的金屬酵鹽類,辛酸鋅、辛酸錫等的有機酸鹽 類。 溶劑則可利用不含會與前述含有矽之化合物(A)和含有 矽及/或氟化合物⑻反應性之羥基者。較好者為脂族烴、 環脂族烴、鹵化烴、矽«烷糸化合物等。脂族烴例如己烷 、庚烷、辛烷、癸烷、異辛烷等。環脂族烴例如環己烷。 芳香族烴例如甲苯、二甲苯、苯、苯乙烷等。鹵化烴例如 三氣乙烷、三氣三氟乙烷、二氯甲烷、二氯苯氟乙烷、全 -20- (請先閲讀背面之注$項再填寫本頁) 袈. 訂
A 本紙張尺度適用中國國家標準(CNS ) A4规格(210X297公釐) 經濟部中央標準局員工消費合作杜印製 515384 A7 B7 五、發明説明(is ) 氦乙烷、全氟己烷、HCFC-141b等。矽氧烷条化合物例如聚矽 氣烷,環聚二甲基矽氣烷等。另外,亦可使用丙酮、甲乙 酮、甲異丙_等酮条化合物,酯酸乙酯、酯酸丁歯等酯類 〇 前述含有矽之化合物(A)與含有矽及/或氟之化合物⑻ 之重童比為1/99〜80/20,較好為2/98〜40/60 ,最好為2/98 〜30/70。如果比1/99為小或者比8Θ/20為大時,則不能生成 良好之交聯皮膜,且有離模性變壞之傾向。 硬化促進劑之用量則依含有矽之化合物(A)和含有矽及 /或氟之化合物⑻之反應性而定,例如為含有矽之化合物 (A)及含有矽及/或银之化合物⑻之總重量之0〜10% ,最 好為1〜7%。如果超過18%則有離模性變壊之傾向。 使用溶剤時,溶劑之置需使溶劑以外之成份的濃度在 0.1〜20 % ,較好是0.5〜10 %,最好是1〜10 %為佳。潑度 如果低於0.1%則有不易形成良好的離模剤皮膜之傾向,如 果超過20%則粘度過高,有不易塗佈之傾向。 本發明之離模剤可《由在常溫下混合含有矽之化合^ (A),含有矽及/或氟之化合物⑻以及必要之溶劑、硬化促 進劑;其他成份而作成一液型。如果在含有矽之化合物和 含有矽及/或氟之化合物的反應性高的情形下可将硬化促 進劑和其他成份的混合物分開保存而作成二液型。 例如本發明之一液型離模劑可在常溫下以刷塗或噴塗 在模具之内倒,在常溫或加熱下形成本發明之硬化皮膜。 加熱溫度依材料而定,通常在250*0以下,較好的是在20〜 -21- 本紙張尺度適用中國國家標準(CNS ) A4^格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 袈· 訂 經濟部中央標準局貝工消費合作社印袈 A7 B7 五、發明説明(19 ) 200t!以下。較0¾為低時,硬化不易進行,較250υ為高的 話具有離模劑成份易於分解之傾向。如果是二液型,則在 使用前才混合硬化促進剤及其他之成份,然後塗佈在模具 之内侧,需要的話可加熱以形成本發明之硬化皮膜。加熱 溫度依材料而定,通常在250Ό以下,較好是在20〜200t!。 較01C為低時,硬化不易進行,較250t:為高的話具有離模 _成份易於分解之傾向。本發明的硬化皮膜之膜厚並無特 別之限制,不論是一液型、二液型,為了得到良好的離棋 性,以0.1〜100W·,特別是0.2〜20//B ,更待別是0.5〜10WB為 佳。 本發明之離模劑之硬化如以脱肟(〇xi»e)型為例則如下 示,首先⑴產生脱肟反應,之後⑵藉由脱水反應或脱醇反 應而進行交聯反慝。 ⑴脱肟反應 \ ^ R ^ Ηο Ω R 3 ^ SiON = —^->^SiOH + HON = \R4 〆 、r4 ⑵脱水反應(交聯反應) 彡SiOH + HO - K1->^SiO - Κ1 + Η20 或脱酵反應(交聯反應)
^SiOH + R7 〇 - Κ2 -> ^SiO - R7 + κ2 0H 〔式子中HO-lt1、R2〇-K2 (R2為硪原子數1〜4之烴基) 乃表示前述之1分子内有烷氣基2掴以上之含有矽及/或 氟之化合物〕。 -22- 本紙張A度適用中國國家標準(CNS ) A4規格(210X297公嫠) ^n· In ^^1· aBi^i 11 al^i ^^^1 ϋ-i· 11 (请先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局員工消費合作社印製 A7 __'_B7__ 五、發明説明(20 ) 使用本發明之離模劑實施以下之成型方法。亦卽,將 前述含有矽之化合物(A)和含有矽及/或氟之化合物⑻以前 述之方法塗佈在模具之内面藉由前述之機構使之硬化在模 具内形成硬化皮膜之後,再將成型用組合物充《入模具内 成形之,再從該模具將成形品脱模。 本發明之離模劑可用於鋁製、不锈銷製、鐵製、琛氣 樹脂製、木製等的模具上,或者用於鐸電鑄或鐸電鍍之模 具之上。 利用本發明之離模劑所離棋之成形品主要為使用聚胺 基甲酸酯發泡體、琛氣樹脂、苯酚樹脂、FRP等熱硬化樹脂 ,胺基甲酸乙酯橡謬、H-NBR、NBR、矽酮橡膠、CR、NR、氟 橡膠、SBR、BR、IIR、IR等橡膠類作為主體之成形用组合物 所製成之成形品。 本發明之離模劑可充填入噴霧罐中以噴射劑之方式使 用。可使用脂族烴、鹵化烴、二氣化硪、氮氣等作為噴射 劑。脂族烴例如丙烷、丁烷、LPG、二甲醚等。鹵化烴例如 R-ll、R-12、HFC-134a、HCFC-1426、HCFC-22、HCFC-141b等在離模剤 中包含有10〜95 %,最好20〜90 %,更好是30〜90 %之噴 射劑。如果噴射劑少於10%則噴射不良,有不能形成均一 之皮膜之傾向。如果噴射劑多於95 %則皮膜變薄,有離模 性降低之傾向。 以下藉由實施例及比較例更進一步説明本發明,本發 明並不限定於這些實施例。 實施例1 -23- 本紙張尺度適用中國國家標準( CNS ) A4規格(210Χ297公釐) —.1 111!- 裝— I 訂 I,^ (請先閲讀背面之注意事項再填寫本頁) Α7 Β7 五、發明説明(21 ) 混合2份(重量份,以下同)之含有矽之化合物CHaSi (ON = C (CHa) 2) a ,93份之1分子内具有羥基或烷氣基二値 以上之含有矽及/或氟之化合物: CH3 ,
I
HO(SiO)tH I (t = 1000) ch3 . ,5份之四(2-乙基己基)鈦酸酯(交聯促進劑)及(甲 苯溶劑)調製成本發明之離模剤。甲苯之量占離模劑之95 %,亦卽其他三成份緦計占5 % 〇 對此離楔劑進行以下之建纗離棋性測試,塗裝性測試 及修整性測試。 〔連鑲離模性测試〕 (離模劑之離模性能及離棋赛命) 以刷塗將離模劑塗佈在内镅尺寸6αιφ + 1 ο之鋁製 模具,藉由將模具在150*0加熱10分鐘使離模劑硬化而在模 具之内側形成硬化皮膜。硬化皮膜之厚度為2.5 /zb 。 將具有下列組成之氨基甲酸乙酯組合物以混合機充份 攪拌之後流入此模具之中。 (請先閱讀背面之注$項再填寫本頁) 年 、tT. 經濟部中央標牟局員工消費合作社印裝
Saniley FA 9121〉 100 份 乙二醇 19 份 R-ll ( 三氛單氟甲烷) 5 份 DABCO Θ.9 份 (1,4 - 二 dr 二環〔2,2,2〕辛烷) 二丁基錫二月桂酸 酯 0.025 份 -24- 本紙張Λ度適用中國國家標率(CNS ) Α4規格(210X297公釐) 經濟部中央標隼局貝工消费合作社印裝 315384 ^ A7 B7 五、發明説明(22 )
Millionate MTL2) 104 份 1) 日本三洋化成工業股份有限公司製之多元醇 2) 日本聚胺基甲酸乙酯工業股份有限公司製之異«酸 酯 在室溫硬化10分鐘成形出胺基甲酸乙酯成形體之後, 以拉伸試驗機(拉伸速度20«« /分)拉伸在胺基甲酸乙酯 成形中預先直立地置於其中之梢以澍出拉伸力(S /Ctf ) 然後對離模性能以下列之基準評價之。 A : 1明g/Cnf以下 B :大於1明g/Crf ; 2明g/Caf以下 C :大於 20Θ g/Cm" ; 300 g/Cnf 以下 D :大於 308 g/Ctf 接箸,不再塗佈離楔劑,重複胺基甲酸乙酯之成形及 離模50次。對第10次、30次及50次成形後之離棋性能作評 價,結果示於表7 〇 〔塗裝性測試〕(成形品之二次加工性) 將以下所示組成之底漆充份混合之後刷塗於在連鑛離 模性換I試之第1次成形後的胺基甲酸乙酯成形體之上。
Planit L « 753> 1的份
Planit L # 75 稀釋剤 100 份 3) 大日本塗料股份有限公司製之丙烯酸条塗料底漆 4) 大日本塗料股份有限公司製之稀釋劑 在80 C乾燥10分鐘之後,在底漆之上在刷塗一層具有 如下所示組成之面漆。 "25- 本紙張Α度逍用中國國家標準(CNS > Α4規格(210Χ297公釐) (請先閲讀背面之注意ί項再填寫本頁) 裟· 訂 經濟部中央標準局貝工消费合作社印裝 A7 __B7_______ 五、發明説明(23 )
Planit S8> 100 份
Planit稀釋劑I» 10« 1明份 5) 大日本塗料股份有限公司製之丙烯酸条塗料 6) 大日本塗料股份有限公司製之稀釋劑 在1001乾燥40分鐘之後,以JIS Κ54ΘΘ之方法進行棋盤孔 目測試,評價測試後之塗膜殘留數。100/1明表示密著性良 好。0/1册表示皮膜完全剌離。结果如表7所示。 〔修整性測試〕 對於連繽離模性測試後之第1次的離棋後胺基甲酸乙 酷成形醴用目視來觀察表面修整性,以下面所示之基準來 進行評價。結果如表7所示。 A:表面修整性狀態良好 B:在部份的表面上可見到針孔 C:在全部的表面上均可見到針孔 實施例1〜21 以和實施例1同樣的方法,但含有矽之化合物、含有 矽及/或氟之化合物、硬化促進劑及溶劑之组成則如表1 〜表5所示調製出本發明之離模劑。依照表1〜5所示之 硬化條件之實施例1同樣的方法形成硬化皮膜。各皮膜之 膜厚如表1〜5所示。 -26- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ^^1- m·* ^^^1 In · ϋ— ϋ.1 ^^^1 ^^^1 —ϋ· 1_1 (請先閲讀背面之注意事項再填寫本頁) 五、發明説明(24 ) A7 B7 經濟部中央標準局貝工消費合作社印製 CO to 1—< ir CH3 1 Si(0N=C(CH3)2)3 CH3 1 Si(0N=C(CH3)2)3 CH3 1 Si(0N=C(CH3)2)3 1 ___ GO 一 〇 M* CC y—N Ca5 o II o 〇 CQ CO cc ώ" 化合物 含有矽之化合物 CO to $ CH3 1 HO(SiO)tH 1 CH3(t=3500) CH3 1 HO(SiO)tH 1 CH3 (t=800) CH3 1 HO(SiO)tH 1 CH3 (t=25) CH3 1 HO(SiO)tH 1 CH3 (t = 1000) 化合物 麯昤 M·掛 Π>^ 漥\ m CO ω CD CO Ol 00 CD CO 四(2-乙基己基) 鈦酸酯 鼬!乙基己基> 罐乙基己基> 四(2-乙基己基) 鈦酸酯 _1 化合物 硬化促進劑 ·〇 cn to cn CJ1 σι cn αι 镟ω 口屮1 -ffl -a -a 溶劑 CD U1 CD ϋΐ CD CJ1 CD Ol 溶劑量 CO Ο Ο 100 CO 〇 *—* Ol o rf 硬化條件: α\ CO ·—- o o ω ο 1—» CO o Ol μ m 膜厚 -27- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)
In- —^i·· 11 ml m· In· « al^i n^i In,一^ (請先閲讀背面之注意事項再填寫本頁) 五、發明説明(25 ) A7 B7 經濟部中央標準局員工消費合作社印製 00 -4 σ> u\ ir CO Μ· CO M· o CO o K3: CO 〇 II <r> y—N <~5 tn CO o 2 o ta C/5 M· 昤 II <r> /«—N o « CO t\5 〇 o a: CO o 〇〇 CC *"*· § II o 化合物 co^ w o CO ^ -|| m CO to ώ" Π> 豸 CO o CO CJl CO o CO o SES o g cq o » o <T5 一 CO — O « m. ca 〇 CO o—一 o η>· P3 CO 〇 CO O — C/3 —* 〇 ca m· cc CO 〇 CO O 一 CO 一 o K i-*· CO 〇 C〇 cv 趣咏 Ν·掛 ✓-N ^ 〇 o 〇 O Λ ^ n> II tu ί 工 cu II 口3 Λ « 1 兹 o o o 漥\ o o cn -Ϊ ϋΐ 铧@ 铧B 铧B 賻^ 蹑〜 IDH tS^ 断1 IN inro 逝I (N mto m i (N CT 唞 1 m m Q> 商 cu D1 [U 眘 m m m m m. ϋΐ 1 a\ cn Η-» CO o 貉ω πί— b b o ffi II Q IN -ffl -ffl •ffl ®ί s ?锜 O 1 \ 1— Hi m cn \ o cr \ CD CO CD m CD CD CD m ai 岫 100 150 150 150 rf m CO 〇 CO o H-1 〇 o 裔 Ol μ-» o o •fc 鍤 ·〇 •to Ul CO 3 m. m· n^i n^i n 1 mi ί nn ^^^1 (請先閲讀背面之注意事項再填寫本頁) -28- 本紙張尺度適用中國國家標率(CNS > A4規格(210X297公釐) 315384 A7 B7 五、發明説明(26 ) 經濟部中央標準局員工消費合作社印裝 *—* 1—* CO ir CH3 1 Si (0N=C(CH3)2)3 CH3 1 Si(0N=C(CH3)2)ii 00— o A ω o 1! o M 〇〇 CH3 Si(0N=C(CH3)2)3 § CO li ο N Ο ο co Cd Wco CJl 化合物 含有矽之化合物 1 . 1丨 :-S iU Ο to o to o to 〇 $ C15F31CH2CH2Si(0H)3 C8Fi7CH2CH2Si(0CH3)3 FOMBLIN Z DOL CH3 C2H50(Si-0)tC2H5 CH3 (t=300) tn o ✓—V 〇— C/5 — 〇 » Μ· tC CO 〇 CO · r+ r^· 1! tl: cn o e 化合物 古1溶 cn -οι Ol Ol cn —· ·. . 四(2~-乙基己基7 球酸嘩 四(2-έ基己基) 鈦酸酯 * <· i?. (N1 m cu m 四(2-乙基己基) 欽酸酯 : g皞乙基己基)' 化合物 硬化促進劑 ω · CJl cn σι CJl α\ ,ϋΐ Ol cn CJl it&f 三纪氟乙烷 三紀氟乙烷 三氛三截乙烷 -η ii桝錨U o :溶劑 CD Οϊ CD αι CD cn CD αι CD CJl 溶劑置 1—» Οϊ ο u\ o t—* Ol o η-* CJl Ο — CJl o r$ 磾化條件‘ to ο CO o CO o CO ο 一 o »—· to b to b Η- ϋΐ 1—* 3 1. 3 -29- 0 (請先閲讀背面之注意事項再填寫本頁) 袈. 訂 本紙張尺度適用中國國家標準(CNS > A4規格(2丨0X297公楚) 五、發明説明(27 ) A7 B7 經濟部中央標準局員工消費合作社印製 H-* Ol — ir r=c<c^ CH3 Si(0N = C(CH3)2)8 化合物 含有矽之化合物 H-* o H-» cn » g g π> ^ 冷 S 〇 忒 巴 * 屮 5 S m 〇=〇 ^ ;:-? H° 〇 cn J· ^ w II HOCH2〇F2CF2〇(Ci2 CF2CF2〇)2〇CF2CF2 CH2〇H tngti O CC O W H- 〇 Q〇 n> ~ 弈3 f s i i=° s 异 曲 ® 〇s=〇 O ·· II 〇—〇 2=0 ^ to 〇 53 1* qw SS Si 化合物 cr^ 0>J51 漥\ .珙 00 Ol 00 ϋΐ 00 o S®fi6Z:,SB^) g益乙基己基r g晶-乙基己基) 化合物 硬化促進劑 Ol ϋι cn Ol σι CJ1 貉ω1 il强 撕 全氟己烷 全氟己烷’ 1 j 三氛三氟乙烷 ㈣ CD αι CD C71 CD Ol 溶劑量 -1 »—ι o o Η- cn ο cn o ' rf 硬化條件 CO o CO ο to o •CJ1 CO • ο »—Λ o μ m 膜厚 -30- I 1 裝 I I 11 u 訂 n 11 τ*^· (請先閱讀背面之注意事項再填寫本頁) 本紙張A度適用中國國家標準(CNS ) A4規格(210X297公釐) 五、發明説明(28)
7 7 A B 經濟部中央標準局貝工消費合作社印製 to to o CD »—· ir CH3Si(0.C(c:H35)3 o tn CO CO H*. S一 o 1 〇 = 〇 co II o n CO s«/ CO ! CH3Si(NH〈^)3 CH3 1 CH3Si(0-C=CH2)3 0 II CH3Si(0CCH3)3 化合物 含有矽之化合物 to ο CO o to o CO o CO o CH3 1 H0(Si0)cH CH3 (c=100) CH3 1 HO(SiO)cH CH3 (c=100) g y—s O— CO— o bd η·· n CO 〇 CO cT ^ η n μ-» O o o y—s ζΛ — U M· » CO 〇 CO «-t· r4* II Cd h-» 〇 s CH3 1 HO(SiO)tH CH3(t=100) 化合物 挪時 雜 i\ 诞 cn CJl Ol ϋΐ C71 辛酸錫 1 辛酸錫 辛酸錫 辛酸錫 辛酸錫. 化合物 ΓΡ; 商丨 m cn 〇\ cn cn CJl cn b CJl b cn •o Ol b Ol o 美晶I 甲苯 甲苯 甲苯 甲苯 甲苯 萌 m CD Ol CD cn CO Ol CD Ol CO Ol 溶劑量 H-* CJ1 o H-* cn o 150 ►—» Cn o »—» Ol o d 硬化條件 o H- o ►—· o H-· o ►—· o ►—· Ol Ol cn Ol — b\ β m 膜厚 ---------r 裝------訂------ i (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 315384 A7 B7 經濟部中央標準局貝工消費合作社印製 五、發明説明(29 ) 對以上逭些皮膜和實施例1同樣地進行連績離模性測 試、塗装性測試及修整性測試。 此外,在實施例8乃使用己烷與二氯一氟乙烷(1«^(:- 141b) 50 : 50 (重量比)之混合物作溶劑。在實施例9乃使 用二甲苯及 _〇H3 ^Si - Ο I ch3 所示之環聚二甲基矽氣烷50: 50 (重量比)之混合合物作 溶劑。此外,在實施例11之中使用之FONBLIH Z D0L (含有矽 及/或氟之化合物)為日本Montedison公司製之化合物(在 全氟聚醚之兩末端具有烷氣基之化合物)。而在實施例14 及16則使用如組合使用表4所示之3種化合物作為含有矽 及/或氟之化合物。 结果示於表7。 l:b較例1〜8 使用表6所示之成份以和實施例1同樣的方法調製出 離模劑。依照表5所示之硬化條件以實施例1同樣的方法 形成硬化皮膜。各皮膜之膜厚如表6所示。
-32- 本紙張^度適用中國國家標率(€奶)八4規格(210父297公釐) (請先閲讀背面之注$項再填寫本頁) 袈· is-.. 五、發明説明(30 ) A7 B7 經濟部中央標準局員工消費合作社印製 00 05 CJl CO CO I-— 總Μ 纖 C3F7CH2CH2Si(0N= C(CH3)2)3 1 巴西棕搁蟠 SH - 7020 SH - 200 350cs Si(0CH2CH3)4 (CH3)2Si(0NC(CH3)2)2 Si_3)4 Si(0CH3)4 π> 眘 8 8 »—» 8 § m ο 〇— C/3 —- Ο ¢13 tc CO Ο 00 r-h <-** ii m ►—* o o 1 1 1 o u CO 2一G 一 2 Cm w« Cm C*i 〇 CO /«-N ^ s*r片 II Cfi to o o CH3 1 CH3(SiO)kH CH3 (k=300) CH3 1 CH3(SiO)kH CH3(k=50) CH3 CH3(SiO)kH CH3 (k=1000) 广 π> 1 1 ci g晶乙基己基 ! 1 g晶乙基己基〉 溫乙基己基) 四(2-乙基己基) 鈦酸酯 化合物 硬化促進劑; αι 1 1 CJl ϋΐ 1 αι b σ> CJl cn CJl ' CJl CO U1 iiml -a 榭 -a Ο) 1 ω tA 1 CO -ffl -ffl -a -a 溶劑 CD CO CO 办 CD σι CO a\ CD Ol CD Ol CD CD ϋΐ 溶劑量 g 1 I 1 1—* . § 8 »—» 8 ►—» 8 <-$ 硬化條件 1—» 〇 i I 1 1—* 〇 CO o CO o ►—· Ο o bi. ►—· ο ο CO ο a\ o b CO b to o CO b 3 藏 锢 -33- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) ---------^-裝— (請先閲讀背面之注意事項再填寫本頁) 訂 Λ 〇lS384 A7 B7 五、發明説明(31 ) 對逭些皮膜和實施例1同樣地進行連壤離模性測試、 塗裝性測試及修整性測試。 此外,比較例5所用之SH-2册,350 CS為東嫘道康寧矽酮 股份有限公司製之二甲基矽氣烷酵,比較例6所用之SH-7020 為東嫘道康寧矽酮股份有限公司製之矽蟠。 結果示於表7。此外,連續離模性測試評價為D者, 其測試次數在其後以括弧表之。 表 7
連娜模性 塗装性 修整性 第1次 第10次 第锨 第漱 実施例1 A A A A 100/100 A "2 A A A B 100/100 A "3 A A A A 100/100 A ·· 4 A A A B 100/100 A "5 A A A A 100/100 A ·· 6 A A A A 100/100 A ” 7 A A A A 100/100 A v 8 A A A A 100/100 A // 9 A A A A 100/100 A 〃 10 A A A A 100/100 A 〃 11 A A A A 100/100 A 〃 12 A A A B 100/100 A 〃 13 A A A B 100/100 A 〃 14 A A A B 100/100 A 〃 15 A A A • A 100/100 A 〃 16 A A A & 100/100 A "17 A A B B 100/100 A "18 A A A B 100/100 A 对19 A A B B 100/100 A 〃 20 A A B B 100/100 A ·· 21 A A A A 100/100 A 比较例1 A A B D(35) 90/100 A // 2 A B D(21) — 50/100 B // 3 A D (8) - - 0/100 c // 4 A D (7) - - 0/100 c "5 C D (2) - - 0/100 c "6 B D (5) 一 - 0/100 B "7 B D (2) — — 0/100 B // 8 A A B D(30) 80/100 A 經濟部中央標準局負工消費合作社印裝 (請先閲讀背面之注意事項再填寫本頁) 本纸張尺度適用中國國家搮準⑼呢^彳规格”丨叫撕公麓) ^4- 315384 經濟部中央橾準局貝工消費合作社印製 A7 B7 五、發明説明(32 ) 從表7之結果可知,使用本發明之離模爾,包括不使 用硬化促進劑之情形,可得到連鑲離模性測試、塗裝性測 試、修整性均良好之結果。 本發明之離模劑,離模性能優良,離模壽命長,同時 成形品之表面修整性良好,由於不會附著於成形品之表面 所以成形品的塗佈性等的二次加工性不會降低。 -35- 本紙張A度適用中國固家樣準(CNS ) A4規格(210X297公釐) I I I 裝^ — I 訂 I I I I I — I i I I ―― I I I I I I I I . .. . (請先閲讀背面之注意事項再填寫本頁) L·.
Claims (3)
- 315384 第831 10816號申請專 . — - ~"―——·-仏圍修居 本 A8 B8 C8 D8 修正日期 8#/0§/2fl9 修正I 補充丨 申請專利範圍·一 1. 一種離模 — Ψ 下列(A) , (B) , (C)及(D)四成份所組成: (A)通式(I)所有矽之化合物 R^S i (式子中,R1為: R3 (I) R3 R3 —Ο — C = CH2 — 0 - N = C<^ — N —C —— NH-/~~\、 \r4 II W R Ο (R3、R4分別為硪原子數1〜4之烴基),R2為碌原子數 1〜4烴基或鹵化之烴基,η為3或4〕;以及 (B)l分子内具有羥基或烷氣基2偁以上之含有矽及/ 或氟之化合物,此含有矽及或氟之化合物乃擇自: (a)通式(m): RfA4A5 (I) (式子中Rf為硪原子數6〜21之全氟烷基,A4為硪原子數1 一 6之烯基,A5為 ο one 2 Ηc Η3 - CIC Ο 或 II ) Ο - CCH = CH2 (請先閲讀背面之注意事項再填寫本頁) 訂 味· 經濟部中央標準局負工消费合作社印裝 所表示之化合物20重悬%以上; ⑸通式(IV): Αβ0Α7Αβ (IV) (式子中丨*>為氫原子;Α7為硪遠子數1〜6之烯基,丨8為 ο one 或- 36- 2 Η C Η 一一 CIC ο II Ο - CCH = CH2 本紙張尺度適用中國國家標率(CNS ) Α4规格(210X297公釐) A8 B8 C8 D8 315384 K、申請專利範圍 所表示之化合物2Χ以上作為共聚合成份,且數量平均分子 鼍為10明以上之共聚合物; (c) 通式(m) R5 I X4 〇~<Si — 0)m_ (Μ) R6 (式子中Rs、Re分別為碩原子數1〜4之烷基,X4、X5分 別為硪原子數1〜4之烴基,β為10至5000); (d) 通式(VI): Y^CHaR^O-R^-R^CHaOY2 (VI) 所表示之化合物,(式子中Y1、Y2、分別為氫原子,818為 (請先閲讀背面之注$項再填寫本頁) 2 F C 2 F C •2 F C 或
- 3 -F F CIC 為 T R1 2 F C
- 3 -F F CIC I 或 1 2 F C 2 F C Rie為由 經濟部中央標率局員工消費合作社印製 -(CF2〇^y、-(CF2CF2〇)^ 及-fR19% 所組成之族 cf3 cf3 中遘出之構造單位之至少1種,R19為-cf2 CF -、- 0:fcf2-或一〇卩2〇卩2〇?2—>$1+52 + 53為5至200);以及 (e)通式(VB)之化合物: -37 - 衣紙張尺度逋用中國國家揉準(CNS ) A4规格(210X297公釐) 315384 A8 B8 C8 D8 經濟部中央揉牟局負工消費合作社印裝 六、申請專利範圍 RfA^HOA^a (VI) 所表示之化合物,(式子中Rf為硪原子數6〜21之全氟烷 基,A1為硪原子數2〜6之烷基,A2為氫原子或硪原子數 1〜4之烷基; (C) 溶劑,以及 (D) 硬化促進; 其中(A)含有矽之化合物與(B)含有矽及/或氟之化合物之 重量比為1/99〜80/20者。 2. 如申請専利範圍第1項所述之離模劑,其中含有矽 之化合物(A)乃為通式U)所示之化合物: R^S i R24-« ⑴ (式子中,R1為: -〇-N = C’r3 \ R4 (R3、R4分別表示硪原子數1〜4之烴基,R2為硪原子數 1〜4之烴基或鹵化烴基,n為3或4)。 3. 如申請專利範困第1項所述之離棋ϋ ,其中該溶剤 為脂族烴,脂環族烴,芳香族烴,鹵化烴或矽氣烷。 4. 如申請專利範圍第1項所逑之離楔劑,其中該硬化 促進劑為金屬烷酵類,或有機酸鹽類者c 5. 如申請専利範困第1項所述之離模剤,其中該通式 0Λ)中之為20至50000 6. 如申請専利範麵修第1項所述之離棋劑,其中該通 -38 - (請先閱讀背面之注意事項再填寫本頁) 乂. 訂 -% 衣紙張尺度適用中國國家橾準(CNS ) A4規格(210X297公釐) 315384 六、申請專利範圍 式(VI)中之ShS^S3為10f將申請專利範圍第1項之含有矽 V或氟之化合物塗佈於模具之内面 7. —種硬化皮 之化合物以及含有矽 並使之硬化而得到。 8. 如申請專利範圍第7項所逑之硬化皮膜,其中含有 矽之化合物(A)乃為通式(I)所示之化合物: RXnS i R24-„ (Π) 〔式子中、R1為: -Ο - N = C R3 R4 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局負工消費合作社印製 RJ R4 (R3、R4分別表示硪原子數1〜4之烴基,R2為硪原子數 1〜4之烴基或鹵化烴基,η為3或4〕。 9. 一種模塑成型方法,包括将申請専利範圍第1項之 含有矽之化合物以及含有矽及/或氟之化合物塗佈於模具 之内面,使之硬化在模具内形成硬化皮膜之後,將成型用 組合物充填於該模具内,再從該模具内將成型品離模。 10.如申讅專利範園第9項所述之成棋塑型方法,其中 含有矽之化合物(Α)乃為通式(Ε)所示之化合物: R^S i R24-n (H) (式子中R1為: Ο - N = C (R3、R4分別表示硪原子數1〜4之烴基,R2為硪原子數 1〜4之烴基或鹵化烴基,η為3或4〕。 -39 - 各紙張尺度適用中國國家標率(CNS > Α4規格(210X297公釐)
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EP (1) | EP0731157A4 (zh) |
KR (1) | KR100254839B1 (zh) |
CN (1) | CN1053005C (zh) |
TW (1) | TW315384B (zh) |
WO (1) | WO1995014750A1 (zh) |
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CA2307115A1 (en) * | 1997-11-10 | 1999-05-20 | Henkel Corporation | Molding facilitator and use thereof |
JP4067718B2 (ja) * | 1999-09-20 | 2008-03-26 | Jsr株式会社 | 樹脂製型の処理法および樹脂製型 |
US7691302B2 (en) * | 2005-05-16 | 2010-04-06 | Prairie Packaging, Inc. | Disposable cup lid |
DE102005054920A1 (de) * | 2005-11-17 | 2007-05-24 | Nitrochemie Aschau Gmbh | Härter für Siliconkautschukmassen |
EP1894975A1 (de) * | 2006-08-30 | 2008-03-05 | Sika Technology AG | Siliconzusammensetzung |
WO2011043386A1 (ja) * | 2009-10-06 | 2011-04-14 | ソニーケミカル&インフォメーションデバイス株式会社 | 離型剤組成物、離型フィルム及びこれを用いた接着フィルム |
CN102189627B (zh) * | 2010-03-04 | 2014-06-04 | 毕建光 | 脱模剂和制备方法及其在制备聚氨酯模制品中的用途 |
US8933001B2 (en) | 2010-03-31 | 2015-01-13 | Chevron Oronite Company Llc | Method for improving fluorocarbon elastomer seal compatibility |
CN103442868A (zh) * | 2011-04-27 | 2013-12-11 | Hoya株式会社 | 附有脱模层的模具的清洗方法和附有脱模层的模具的制造方法 |
CN102744815A (zh) * | 2012-07-19 | 2012-10-24 | 湖南罗比特化学材料有限公司 | 一种聚氨酯发泡脱模剂及其制备方法 |
US20160002377A1 (en) * | 2014-07-01 | 2016-01-07 | Taiwan Fluoro Technology Co., Ltd. | Mold releasing agent |
CN106883910A (zh) * | 2017-01-18 | 2017-06-23 | 广州雷哲科技有限公司 | 一种自润滑抗磨修复剂 |
CN109207244B (zh) * | 2017-06-30 | 2021-10-26 | 北京市建筑工程研究院有限责任公司 | 一种混凝土预制构件用水性脱模剂 |
CN111303432A (zh) * | 2020-04-24 | 2020-06-19 | 厦门市豪尔新材料股份有限公司 | 一种聚硅氧烷预聚体、包含其的脱模剂及制备方法 |
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-
1994
- 1994-11-18 WO PCT/JP1994/001961 patent/WO1995014750A1/ja not_active Application Discontinuation
- 1994-11-18 KR KR1019960702691A patent/KR100254839B1/ko not_active IP Right Cessation
- 1994-11-18 US US08/646,374 patent/US6074588A/en not_active Expired - Fee Related
- 1994-11-18 EP EP95900924A patent/EP0731157A4/en not_active Ceased
- 1994-11-18 CN CN94194244A patent/CN1053005C/zh not_active Expired - Fee Related
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CN1053005C (zh) | 2000-05-31 |
CN1135769A (zh) | 1996-11-13 |
KR960705905A (ko) | 1996-11-08 |
EP0731157A4 (en) | 1997-02-19 |
KR100254839B1 (ko) | 2000-05-01 |
WO1995014750A1 (fr) | 1995-06-01 |
US6074588A (en) | 2000-06-13 |
EP0731157A1 (en) | 1996-09-11 |
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