TW201779B - - Google Patents

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Publication number
TW201779B
TW201779B TW79109686A TW79109686A TW201779B TW 201779 B TW201779 B TW 201779B TW 79109686 A TW79109686 A TW 79109686A TW 79109686 A TW79109686 A TW 79109686A TW 201779 B TW201779 B TW 201779B
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TW
Taiwan
Prior art keywords
amine
mixture
resin
item
ministry
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Application number
TW79109686A
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Chinese (zh)
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Ciba Geigy Ag
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Publication of TW201779B publication Critical patent/TW201779B/zh

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五、發明説明(1 ) A6 B6 經濟部中央標準局印製 和是 黏撤反至之 進定據所體 穎劑長劑當 胺別 低成預用用溫溫安。非漬 新化延化適 ,特 ,變劑使使低室存求起預 。硬可硬擇 劑, 脂轉化-所在在儲需引和 劑段亦醇選 化備 樹脂硬常,此需之之此性 着階性硫由。 硬製 氧樹與通中因勿限別而撓 粘 B 定 \ ,值 潛之 琛此分。法,,拘待-可 脂離安胺性數 之物 之將部用方異後一無成, 樹分存用撓之含 定成 劑可下作有差應有並形性 氣全儲使可要包 特生 溶。件成既之反具性的鈷 環完的産之需 , 和接 有脂條形在當劑僅黏段 _ 之段體生物所物 脂絡 具樹制之。相化卽膠階於 點階漬段漬何合 樹及 無氧控段劑有硬體和 B 關 缺 C 預階預任混 氧以 用環慎階化示與漬性製如 述由時 B 加整之 琿, 使醱謹 B 硬表應預撓複例 所藉同,增調化 有物 俗固在之之不反而可確, 有可-外示可硬 含合。常度,謂性中預,於精象 具物別另顯乎可 於混品通黏體所應性}接對難現。不合區。-幾於, 闢化製體高漬般反應段絡體頗動性發混以月果刖關脂 偽硬層清和預一同反階之漬示變定開脂加傾結醇係樹 明可和頂體乾即不於 B 步預顯質安已樹性幾之硫明氣 發之體産液至此種劑到一此驗品存今氧應至物和發環 本醇浸生,性。二化達更。經之儲如環反天合胺本} 硫預 度粘應少硬 ί 行性由需的 之的幾混之(a ......................................................^..............................^.............................. 一請先閱讀背面之注意事項再填寫本頁) 甲 4(210X 297 公沒) A6 B6 五、發明説明(2 ) (b)僅在至少8〇υ溫度下開始反應之潛環氣樹脂硬化劑 (由DSC以ίου/分之加熱速率計算), (C)具有至少一種胺氫之胺及 (d)具有至少一種SH基之硫酵, 其中胺(c)至少有二傾氫原子連結一種以上氮原子或 至少二傾S Η基之硫醇,在D S C圖中以1 0 t: /分之加熱比率 反應則其高峰間之差數至少為3010。 當此混合物在DSC裝置(DSC =差示掃描熱置計)中加熱 時,DSC圔(反應之熱函作用溫度功能)表示二痼顯著之 高峰和淨基線。最初之反應,侬所選擇之組成物,例如 在約80至約130*0之範圍,其最大值像歸因於樹脂和胺/ 硫醇混合物(B階段)之反匾並加以測出,。又,在約1〇〇 至200,最好為約130至18〇υ之範圍由潛硬化劑測出絡 {請先閲讀计面之注意事項再填寫本頁) 預 造 製 物 合 混 用 使 則 大 愈 異 差 。度 果溫 結間 值峰 大高 最應 二反 第二 之在 接 異 差 之 間 峰 高 應 反 中 〇 物佳 合為 混者 在 Ρ ο 0 5 高少 愈至 性以 定而 安 , 存 Ρ 儲40 之為 體少 浸至 基下 0Η在 有存 含之 與體 脂合 樹複 氣胺 環/一二 掲彳 6 0 15三 o’定 no br 3 特 1,在 書 , 明物 說合 利化 專之 國基 «1 英SH 或 如澆 例為 ,作 劑 , 化類 硬脂 知樹 習之 之级 用 高 脂成 樹接 氣絡 環劑 用化 利硬 C 媒 應觭 反或 之類 步酐I , 進類 作胺 經濟部中央標準局印裂 為 做 可 均 物 合 化 之 0 用 用有 使何 物任 合中 化術 封技 塗脂 或樹 劑氣 着環 黏在 脂常 樹通 縳 甲 4(210X 297公发) or‘ A6 B6 五、發明説明(3) 脂 樹” 氣為 琛子 之例 物之 合脂 混樹 明氣 發環 本 用 使 油 甘 水 縮 基 甲 在点地 令或當 俗酵適 ,氛下 酯表在 —有存 別之 分齡 和在 物傜 合應 化反 卢之 。 -(基得 聚羧獲 和値而 酯二應 油有反 甘具醇 水少氱 縮至表 聚中· } 子 I 分 基 甲 化 之 基 羧 個 二 有 具 少 至 中 子 分 在 為 做 可 類 酸 羧 聚 c 族 -7 旨 yyA— HH 進 二體 戊三 ,或 酸化 珀體 琥雙 .或 酸酸 草二 為壬 子 , 例酸 之二 類辛 酸 , 羧酸 聚二 些庚 該 , C 酸 用二 使己 物· 合酸 酸 酞 氫 四 如 例 類 酸 羧 聚 族 脂 環 。用 酸使 油可 仁亦 麻 , 亞又 化 甲 或 酸 酞 異 。酸 酸酞 酞如 氫例 六 , 基類 甲酸 4-竣 或聚 酸族 酞香 氫芳 六用 ,使 酸可 酞 , 氫者 四再 基5. Description of the invention (1) A6 B6 Printed by the Central Bureau of Standards of the Ministry of Economic Affairs. Non-staining, modernization, extension, adaptation, and special agents make the low room need to be anticipated. Hard can be hard to choose the agent, fat conversion-located in the storage and demand lead and the agent section is also alcohol selection and preparation of resin is often hard, this need is due to the order of sulfur. Hard Oxygen Tree and Tongzhong are sticky because they don't need to be limited. It is worth the potential. Law, and wait for-the difference between the number of fats and amines will be different after the use is different. May want to make special solution. The piece needs to be produced with an anti-cobalt ring, and it is connected to a fat strip in the local body of the adhesive. Phased rubber grades in point-stage stains, He Heshu and anaerobic control agents have hardware and B. Defective C. Pre-ordered pre-mixed oxygen to use ring-level caution and staining system as described by B With the addition of Hun, the hard-faced table should be the same as the pre-scratch case. It is not only true that there is a vulgarity in addition to the modulation, but it can be confirmed by the external indication. Frequently, the predication is predictable, and the physical characteristics of the spermatozoa are also obviously more suitable for the blending of the product and the sticky body. Incompatible area. -A few days ago, the reaction system of the high-stain-like reaction segment of the body-building system was mixed with the moisturizing compound and the pseudo-hard layer and the pre-sequence of the pre-stained stains showed that the fat was added and the alcohol was added. The acrosomal stem is the body fluid of the sulphur-bearing gas which has been preliminarily confirmed in step B. This kind of agent will be soaked in this kind of agent until the test sample is stored. Dhd. The storage of the classics such as cyclic anti-heparin amine} sulfur pre-stick should be less hard and the performance is mixed by the need (a ..................... ........................... ^ ................ ............. ^ ........................ Please read the back first Please fill in this page again) A4 (210X 297 public) A6 B6 V. Description of the invention (2) (b) Latent ring gas resin hardener that starts the reaction only at a temperature of at least 8〇υ (by DSC to ίου Calculation of heating rate per minute), (C) an amine having at least one amine hydrogen and (d) a sulfatase having at least one SH group, wherein the amine (c) has at least a dip hydrogen atom connected to more than one nitrogen atom or at least two The mercaptan with a dip S Η group reacts with a heating rate of 10 t: / min in the DSC chart, and the difference between the peaks is at least 3010. When this mixture is heated in a DSC device (DSC = Differential Scanning Calorimeter), DSC (the reaction's enthalpy temperature function) represents the significant peak and net baseline of Erhu. In the initial reaction, the composition selected by Nong, for example, in the range of about 80 to about 130 * 0, the maximum value is attributed to the anti-plaque of the resin and the amine / thiol mixture (stage B) and measured. In addition, in the range of about 100 to 200, preferably about 130 to 18〇υ measured by the latent hardener complex (please read the precautions of the plan first and then fill out this page) Big difference. The peak value of the inter-temperature value of the fruit temperature should be the highest and the second should be the second. The peak height should be the middle of the difference between the difference. The best combination is the mixed one at ρ ο 0 5 40 is the body less immersed under the base 0Η in the presence of the body fat synthesis tree re-enriched amine ring / one two 漲 彳 6 0 15 three o'ding no br 3 special 1, in the book, said the good things The national base of the chemical specialty «1 Ying SH or as an example, as an agent, the level of chemical stearin is known to the level of the tree with high fat into a tree to connect the gas ring agent with a hard C medium should be reversed or similar step anhydride I, classified as amine, the Central Standards Bureau of the Ministry of Economic Affairs, it can be used as a homogenous compound. It is used for any combination of chemical sealing technology, grease or tree gas, and the ring is stuck to the fat tree. 4 (210X 297 public) or 'A6 B6 V. Description of the invention (3) Fat tree "Qi is an example of Chen Zi, a mixed fat mixed tree, Ming Qi hair ring is used to make the oil glycidyl base at a certain place. Or when the yeast is suitable, the ester is present under the atmosphere-there is a difference in age and the combination of the material and the anti-Lu Lu.-(基 得 聚 carboxy 得Ethylene diester oil should have anti-glycol water and less condensed to epipolymerization. -7 Purpose yyA- HH into the second body of glutaric acid, or acidified allium succinate. Or acid acid oxalate as a seed, for example, the second type of acid octanoic acid, carboxylic acid polyheptane, C acid with two hex · Synthetic acid phthalocyanine four examples are acid carboxypolyaliphatic alicyclics. Use acid to make the oil can also be anesthetized, sub-reduced methyl or acid phthalide iso. Acid acid phthalide phthalate such as hydrogen Example six, based formic acid 4- complete Or polyacrylic acid phthalocyanine hydrogen aromatic six, make acid can be phthalic

0 用 即 随 及 以 下 在 存 之 媒 觸 酸 在 或 下 件 。條 酸性 甲齡 二在 苯} 對 K 具 少点 至或 使醇 理氣 處表 及 基 羥 性 醇 之 由 0 種二 有 ΠΊΤ 基衍 油僳 甘類 水醚 縮之 基型 甲類 -此 β· 聚 得 獲 可 應 反 0 醇醚 氮 表 基 甲 和聚 基或 羥醚 性油 酚甘 或水 ,縮 酵二 乙二 醇二 乙 如 類 醇 形 環 非 (請先閲讀背面之注竟事項再填寫本頁) .襄. ,訂· .線· 聚 之 级 高烯 和丙 醇二 乙 烷 丙 醇二 乙 烯 乙 氣 氣 /V - 聚 或 醇二 烷 丙 0二 烷 聚 f 酉二 經濟部中央標準局印製 烷油 戊甘 醇醇 二三 乙6- , 撺,4 甲-2 四烷 氣己 烷 己 醇二 烷 丙 醇 甲 三 , 四 醇戊 二季 甲 4(210>,: 297公沒) :0177^ A6 B6 五、發明説明(4) f請先閲讀背面之注意事項再填寫本頁) 酵,山梨糖醇以及聚表氣醇。 再者,此種化合物亦為衍自琛脂族酵類如1,4 -琛己烷 二甲醇,雙- (4-氫琛己基)-甲烷或2,2-雙- (4-氫琿己基) -丙烷,或具有芳香族核,如Ν,Η-燹-(2-氫乙基)苯胺或 ?,卩’-雙-(2-氫乙胺基)-二苯甲烷。 環氣化合物亦可衍自單核酚類,例如衍自間苯雙酚或 氳醞;或以聚核酚類為基礎,例如雙- (4 -氫苯基)-甲烷 ,4,4’-二氫聯苯,雙-(4-氫苯基)-亞《, 1,1,2,2-四 .訂. 傾- (4 -氫苯基)-乙院,2, 2 -雙- (4 -氳苯基)-丙院,2,2-雙-(3,5 -二溴-4-氫苯基)-丙烷或以酚醛清漆為基礎由 醛類,如甲醛,乙醛,氣醛或糠醛與酚類如酚,或與在 核中由氯原子或Ci -Cs烷基,例如4 -氮酚,2 -甲基酚 或4-第三丁基酚之縮合作用,或與如上所掲示雙酚類之 縮合作用可獲得者。 I)由表氣醇與含有至少二艏胺氫原子之胺的反應生成 物之脫氫氱作用可獲得聚- (N -縮水甘油基)化合物。該 些胺類之例子為苯胺,正丁基胺,雙-(4-胺苯基)-甲烷 ,間-二甲苯二胺或雙- (4 -甲胺基苯基)-甲烷。 •線. 聚- (H -縮水甘油基)化合物亦包括有三縮水、油基異氰 酸酯,環烷撺脲類之Ν,Ν’-二縮水甘油基衍生物,如乙 烯脲或1,3 -丙烯脲,以及乙内醛脲之二縮水甘油基衍生 物如5,5-二甲基乙内醯脾。 IV)聚(S -缩水甘油基)化合物,例如為衍自二硫醇類, -6 - 甲 4(210Χ 的7 公; A6 _ B6 五、發明說明(5 ; 如乙烷-1,2 -二硫醇或雙- (4 -惊甲苯基)醚之二-S -縮水 甘油衍生物類。 V)環脂族環氣樹脂類,例如雙-(2 ,3 -瓌氣琛苯基 2,3 -琛氣琛苯基縮水甘油醴,1,2 -雙- (2,3 -琿氣琛戊氣 基)-乙烷或3,4-璟氣環己甲基3'4'-琿氣環己烷羧酸邇。 再者,可資使用之琿氣樹脂其中1,2 -瓌氣基像結合於 不同之雜原子或官能基,該些化合物包括,例如,4-胺 基酚之Ν,Ν,Ο-三縮水甘油衍生物,水楊酸之縮水甘油醚 /縮水甘油酯,Ν -縮水甘油基- Ν'-(2 -縮水甘油氧丙基)-3,5 -二甲基乙内醯脲或2 -縮水廿油氣基-1,3 -雙- (5,5 -二 甲基-卜縮水甘油乙内醛唳-3 -基)-丙烷。 適宜之琛氣樹脂偽具有2至10克當量/仟克之琛氣含 量其係縮水甘油醚,縮水甘油或芳香族,雜芳族,琛脂 族或脂族化合物之Ν -縮水甘油衍生物。 特別適宜之環氣樹脂為多羥的酚類,例如2,2 -雙- (4- 羥苯基)-丙烷(雙酚Α)或雙- (4-羥苯基)-甲烷(雙酚F), 或酚醛清漆。所使用之環氧樹脂宜為液體,亦卽其偽為 液體樹脂或固體和液體樹脂之液體混合物。 (請先閲讀背面之注竟事項再填寫本頁) k. •訂. 酚 雙 或 A 酚 雙4' 為4, 脂或 樹漆 氣清 環醛 之酚 用酚 適甲 最氧 環 基 胺二 醸 油 甘 水 縮二 之 甘 水 縮 四 烷 甲 基 笨 •線· 劑 化 i ^ 0 0 類潛 物之 生用 衍使 基所 油 的 百 此 成 達 以 可 為 乃 上 則 原 在 經濟部中央標準局印製 呈之 脂接 樹絡 氣與 環但 對 r 即80 , 度 定溫 界定 所限 明之 發定 本界 如於 ,低 物物 合 合 化化 知何 習任 何的 任性 之惰 甲 4(210X 297 公发) 0177^1 A6 B6 五、發明説明(6) 度 ο 溫10 定是 限別 此特 出 , 超 P 而85 應為 反宜 速少 迅至 脂溫 樹限 之 熱 潛 用 使 所 明 發 本 知 習 屬 偽 物 合 化 此 如 例 胍 基 氰 胺 0二 氰二 為 。子 者例 用之 應劑 資化 可硬 上潛 業之 商當 為適 而 9.如 5 笔 8 例 4 , 利 0 專胺 國族 美香 或 或 芳胍 ,或 物, 合 《 化亞 之基 示苯 掲二 所基 51胺 ,4二 如(2 例1-, 如 類 , 胺)0類 聚品唑 之産眯 良司基 改公醯 或學N- ,化如 胍佳例 雙安, 基5(劑 苯14化 甲20硬 o-β 潛 - e 1 1 C 之 如 a 宜 ,ca適 類An 酷 苯 基 甲 三 利 專 國 参 於 £ !1示 掲 像 物 合 化 或 唑 眯 基 苯 此本 0 曰 唑或 眯01 丙3’ 異87 - 5 2 , 1 4 醯和 豪 2 ^ 9 專 國 如 體 合 複 鹽 鼷 金 之 類 唑 眯 為 劑 化 20硬 21之 3,當 74適 利又 專 6 拼 3’ 0 利二 或 酸’ 二類 己物 如生 ,衍 W 嗪 醛三 酸’ 羧I# 之 _ 示酸 掲茴 所氨 78或 9,8# 77酷 6,二 Ί5 酸 酞 00異 {請先閱讀背面之注意事項再填寫本頁) .菸. •訂. 如 例 例 胺 _Kr-不 三1掲•基“ si# -«物 基月Η 胺{ △ r 一 I三之 -6S-提 -4基〶 £¾ 苯It最2-V 如 基類 7 桂物24 月生0, _ 行 3 2^0 或其3, —和利 胺專 密國 及美 丨於 胺 胍 並 苯 酸 醋 利氰 專 -國鹽 美酸 如醋 ,氰 物- 合 化 基 0 乙 氰 為 劑 化 BC 硬潛S 之52 當 3 適28 雙 醇二 乙 基 戊 新 之 載 掲 •線· 經濟部中央標準局印裂 或 鹽 酸 醋 氰- 雙 撺 甲 己 - 0 6-鹽 1酸 ,醋 按8 氰醯T 基雙 丁醇 異甲 烷 己 環 甲 4(210X 297 乂发) A6 B6 五、發明説明(7 ) H-氛醯基醯胺化合物.例如Ν,Ν’-二氰基己二酸二醛 胺為適宜之潛硬化劑。又此化合物俗掲載於美國專利 4,529,821, 4,550,203及 4,618,712。 其他適宜之潛硬化劑偽掲示於美國專利4,694,096之 醯硫丙基酚類和美國專利3,386,955所掲示之脲衍生物 類,例如甲苯- 2,4 -雙- (N,H -二甲基脲>。 適宜之潛硬化劑為4,4’-二胺基二苯基亞《.尤其是 二氰二醛胺。 適當者,本發明之混合物亦可包含與潛硬化劑絡接反 應用之促進劑(e)。適宜促進劑(e)之例子為麻衍生物如 ^-二甲基-^'-(3-氣-4-甲苯基)屏(氣甲苯),1^’-二 甲基- N'-(4 -氣苯基)-P (單糖醛)或Ν,Ν’ -二甲基-H'-(3 ,4-二氰苯基)二脲(雙糖醛),2,4-雙- (Ν,Ν’-二甲暇基) -甲苯或1,4-雙- U’,Ν’-二甲脲基)-苯。所使用之該些 化合物偽掲示於上述美國專利4,283,520。又,掲載於 美國專利1,192,790之脲衍生物亦靨一種合適之促進劑 (請先閱讀背面之注意事項再填寫本頁) •訂. 經濟部中央標準局印$!. 甲Ϊ 如啶化 ί 甲 1- 1 ,啉氰 ,-4物基或 唑基 合胺銨 眯乙 化4~化 基2-銨,溴 苯或 季酚基 - up - t 2¾ 或}了 ,眯 鹽基三 唑基 其乙苄 咪甲 -基或 基4-類胺銨 乙£ 。胺甲化2- w_ 三 1 一M ,-z進第-(基 唑-2促為三甲 眯基之劑6-四 如乙當進4,. 例氰適促2,鹽 ,1-為之,酚 類,亦宜胺銨 唑唑唑適甲苯 眯眯咪又二三 基基 苯, .線· 甲 4(210X 297 公发) 五、發明説明(8 A6 B6 銨;鹼金屬醇鹽,如2,4 -二氫基-3-羥甲基成院之納醇 鹽。 掲載於EP-A200,678之氪齡固賭溶液以及酚/醛樹脂, 和掲示於EP-A351,365之聚合酚類的曼里期(Mannich) 鹺類亦為適宜之促進劑。 最佳之促進劑(e)為眯唑類或麻衍生物類。 如所提本發明混合物之胺組成份(c)傺至少具有一個 胺氫之任何胺。為能獲得良好之結果,胺(c)或硫醇(d) 至少需包含有對環氣樹脂呈活性之三掴氫原子。如為胺 條 此 與 要 只 0 子 原 0 個二 少 至 有 合 結 需 則 況 情 之 第 上 以 PC 種 有 含 類 胺 ο 用 使 皆 胺 何 任 上 則 原 致 一 件 類 胺 環 雜 及 族 香 芳 族 脂 環 。族 子脂 原為 氮例 三適 第之 或} 二(C 第類 ,胺 雙胺胺N, 如辛二 , ,正戊胺 基,3 苯T 氨烷 4-丙 烷 甲 胺二 胺二 撺 甲 六 雙 {請先閲讀背面之注意事項再填寫本頁) .故. i 2 RM » 樹-1 0 基 甲甲 / 胺 苯 二 雙 胺 三 烯 乙 胺 基 苄 新 yfv 胺二 丙 基 丙 胺 戊 烯 乙 四 胺 四 烯 乙 三 胺 甲 ! \1/ 基 丙 胺 ,和 胺2-己1, 烯 , 乙胺 戊二 ,基 胺苯 - 烷 烷己 己環 乙基 三胺 4-一一 胺 間 .訂. 雙 胺 甲己 二環 -基 .線. 雙 烷 甲 - \—/ 基 基 胺 及 烷 丙- 基 己 環 基 氨 基: 己? 環基 甲甲 3 肢 烷 甲 雙 異 /IV 胺 己 環 甲 三 經濟部中央標準局印製 啉 唑 眯 基 胺 聚 雙 和 胺 ),族 胺脂 二由 酮可 爾物 佛合 和 化 此 如 例 胺 0 基 胺 聚 胺 之 當 適 0 得 獲 酸 肪 脂 化 體 甲4(210〆297公发) A6 B6 五、發明説明(9 ) (c)為聚氣烷撑胺類,習知者為由Texaco所産製之 Jeffa^ines® ,例如 Jeffanines® E0R148.D230, D400 或 T403o 又適當之胺類為1,14-二胺基-4,11-二噁十四烷,二 丙烯三胺,2-甲基-1,5-戊二胺,Ν,Ν’-二琿己基-1,6-己二胺,Ν,Ν’-二甲基-1,3-二胺基丙烷,Ν'-二乙基-1,3-二胺基丙烷,Ν,Ν-二甲基-1,3-二胺基丙烷,第二 聚氣丙烯二胺類和三胺類,例如Texaco産製之EPS7315 和EPS7325,2,5-二胺基-2,5-二甲基己烷,雙-(胺甲基) -三環戊二烯,間-胺苄基胺,1,8 -二胺基-對甲烷,雙_ (4-胺基-3,5-二甲環己基)-甲烷,1,3-雙-(胺基甲基)-環己烷,二戊胺,雙- (4 -胺基-3,5 -二乙苯基)-甲烷, 3,5-二乙基甲苯-2,4 -二胺和3,5-二乙基甲苯-2,6-二胺 (請先閲讀t面之注意事項再填寫本頁) -訂. 作 W 0 個 油 二 甘 少 水 至 縮 為 用 別 使 特 不 而 好 餹 最 一 , 有 胺 少 族 至 脂 宜 和 } 族 。(c 脂份類 環成胺 用組之 使之用 偽脂使 如樹所 為 基 份 成 組 之 宜 適 最 物 合 混 明 發 本 胺 族 脂 或 族 § β 環 為 .線. 者 適 合 具 最 中, ® 類 Γ 胺du 族ΓΟ 脂 E 環 0 在之 〇 售 類市 即 由 如 例 烷 己 環 基 胺 二 AG甲 g 基 in氨 經濟部中央橾準局印装 ,基 ?己 基環 胺 基 己 環 甲 三 雙 物 合 化 ),之 胺VI 二或 酮 I 爾式 佛啉 異唑 νίν 眯 基 胺 聚 和 烷 甲 基 胺 甲 4(210X 297 公尨) 五、發明説明(10) A6 B6 H2N-R-NH2 (I), H2N~(-CH2CH20)aCH2CH2NH2 (Π), CH3 CH,0 Use immediately with the following media stored in the next or next. Strips of acidic diamines in benzene} have less than K to or make alcohols and gaseous bases and base hydroxy alcohols from 0 kinds of two bases with a ΠΊΤ group derived oil glycan water ether condensed type A-this β · Polymerization can obtain anti-0 alcohol ether nitrogen epimethyl methyl and poly or hydroxy ether oleyl phenol glycerol or water, shrinkage diethylene glycol diethyl alcohol-like ring-shaped non- (please read the notes on the back of the matter first Fill in this page). Xiang., Set ·. Line · poly-grade high-ene and propanol diethane propanol diethylene ethane gas / V-poly or alcohol dialkyl propane 0 dioxane poly f Unitary Ministry of Economy Central Printed by the Bureau of Standards, Alkanol pentanyl alcohol ditriethyl 6-, 撺, 4 A-2 tetrakane gas hexane hexanol dialkyl propanol trimethyl tri, tetra alcohol pentane quaternary 4 (210> ,: 297 public ): 0177 ^ A6 B6 V. Description of the invention (4) f Please read the precautions on the back before filling this page) Yeast, sorbitol and polyepichlorohydrin. Furthermore, this compound is also derived from aliphatic fatty enzymes such as 1,4-hexamethylene dimethanol, bis- (4-hydrohexyl) -methane, or 2,2-bis- (4-hydrohexyl) )-Propane, or having an aromatic nucleus, such as Ν, Η- 燹-(2-hydroethyl) aniline or?, I'-bis- (2-hydroethylamino) -diphenylmethane. The ring gas compounds can also be derived from mononuclear phenols, such as resorcinol or diethylphenol; or based on polynuclear phenols, such as bis- (4-hydrophenyl) -methane, 4,4'- Dihydrobiphenyl, bis- (4-hydrophenyl) -Asia ", 1,1,2,2-four. Order. Pour- (4-hydrophenyl) -Beiyuan, 2, 2-bis- ( 4-氲 phenyl) -propanol, 2,2-bis- (3,5-dibromo-4-hydrophenyl) -propane or based on novolac from aldehydes, such as formaldehyde, acetaldehyde, gas aldehyde Or furfural and phenols such as phenol, or in the core by the chlorine atom or Ci-Cs alkyl, such as 4-nitrophenol, 2-methylphenol or 4-tert-butylphenol condensation, or as above Shows the availability of the condensation of bisphenols. I) A poly- (N-glycidyl) compound can be obtained by the dehydrogenation of the reaction product of epigas alcohol and an amine containing at least a bis enamine hydrogen atom. Examples of such amines are aniline, n-butylamine, bis- (4-aminophenyl) -methane, m-xylenediamine or bis- (4-methylaminophenyl) -methane. • Line. Poly- (H-glycidyl) compounds also include N, N'-diglycidyl derivatives of triglycidyl, oleyl isocyanate, naphthenic urea, such as ethylene urea or 1,3-propene urea , And diglycidyl derivatives of hydantoin, such as 5,5-dimethylhydantoin. IV) Poly (S-glycidyl) compounds, for example, derived from dithiols, -6-A 4 (210X of 7 male; A6 _ B6 V. Description of the invention (5; such as ethane-1,2- Dithiol or bis- (4-tolyl) ether bis-S-glycidyl derivatives. V) Cycloaliphatic ring gas resins, such as bis- (2,3-pyrrole gas phenyl 2, 3-Chen Qi Chen phenyl glycidyl alcohol, 1,2-bis- (2,3-Heng gas pentanyl)-ethane or 3,4- Jing gas cyclohexyl 3'4'- Hun gas Cyclohexane carboxylic acid. In addition, available Hun gas resins in which 1,2-benzyl groups are bonded to different heteroatoms or functional groups, these compounds include, for example, N of 4-aminophenol , Ν, Ο-triglycidyl derivative, glycidyl ether / glycidyl ester of salicylic acid, Ν-glycidyl-Ν '-(2-glycidoxypropyl) -3,5-dimethylethyl Internal urea or 2-glycidyl oil-based-1,3-bis- (5,5-dimethyl-glycidyl hydantoin-3-yl) -propane. Suitable resins have 2 to 10 gram equivalent / thousand grams of gas content is glycidyl ether, glycidol or aromatic, heteroaromatic, aliphatic or aliphatic compound N-glycidyl derivatives. Particularly suitable ring gas resins are polyhydric phenols, such as 2,2-bis- (4-hydroxyphenyl) -propane (bisphenol A) or bis- (4-hydroxybenzene Base) -methane (bisphenol F), or novolac. The epoxy resin used should be liquid, but also pseudo-liquid or a liquid mixture of solid and liquid resin. (Please read the notes on the back before reading (Fill in this page) k. • Order. Phenol bis or A phenol bis 4 'is 4, phenolic or lacquer gas-clear cyclic aldehyde phenol is suitable for phenol, methyl oxycyclylamine, diglycerin, glycerin, and glycerin. Tetramethylmethylbenzine · Line · Agent i ^ 0 0 The bio-derived derivative of the base type of submersibles is considered to be acceptable, but it was originally printed in the Central Standards Bureau of the Ministry of Economic Affairs. The qi and the ring, but the r is 80, the temperature is limited by the definition of the temperature, and the bounds of the world are as the same. The combination of low material and chemical knowledge is any wayward lazy armor 4 (210X 297 public) 0177 ^ 1 A6 B6 V. Description of invention (6) Degree ο Temperature 10 is the limit and it is unique. Super P and 85 should be the speed limit and the temperature limit of fat temperature. The thermal latent application makes the known quasi-pseudo-chemicals combined into an example, such as the guanidinocyanamide 0 dicyandiamide. The application of the agent in the case of the application can be hardened by the commerce of the dive industry. 9. 5 strokes 8 cases 4, Li 0 special amines of the national family Meixiang or or guanidine, or the compound, the combination of the subunits of oxybenzene shows benzyl diisothiol 51 amine, 4 di (such as 2 cases 1-, such as amine) The production of class 0 polypyrazole can be changed from serotonin to acetyl or N-, such as guanidine, good example, shuangan, base 5 (agent benzene 14, methyl 20, hard o-β latent-e 1 1 C, such as a, ca Appropriate An Ku phenyl benzene three Sanli special country participate in £! 1 shows the combination of the compound or oxazolyl benzene this book 0 azole or squint 01 propane 3 'iso 87-5 2, 1 4 醯 和 豪 2 ^ 9 A special country such as a compound salt such as gold and azole is a compound 20 hard 21 to 3, when 74 is suitable and special 6 fight 3 '0 Li Er or acid' two kinds of self-like things, such as derived W azine Aldehydic acid 'Carboxy I # of _ shows acid 78 or 9, 8 # 77 cool 6, two Ί5 acid phthalate 00 different (please read the precautions on the back before filling this page). Smoke. • Order. For example, amine_Kr- 不 三1 掲 • 基 “si #-« Material-based moon amine {△ r 一 I 三 之 -6S- 提 -4 基 〶 £ ¾ Benzene it most 2-V such as base 7 Guiwu 24 Monthly birth 0, _ row 3 2 ^ 0 or its 3,-and Liamine special secret country and the United States amine guanidine benzoic acid vinegar cyanide special-national salt medicinal acid such as vinegar, cyanide-complex group 0 ethyl cyanide as agent BC hard Latent S of 52 when 3 suitable 28 bis-alcohol diethylpentyl cyanide · line · Central Ministry of Economic Affairs of the Ministry of Economic Affairs or cracked vinegar or cyanogen chloride-diazepam-0 6- salt 1 acid, vinegar according to 8 cyanohydrin T-based bis-butanol isomethane hexamethylene 4 (210X 297 异 发) A6 B6 Fifth, the description of the invention (7) H-atmoyl amide compound. For example, Ν, Ν'-dicyanoadipate dialdehyde amine It is a suitable latent hardener. This compound is contained in U.S. Patent Nos. 4,529,821, 4,550,203 and 4,618,712. Other suitable latent hardeners are shown in US Pat. No. 4,694,096, sulfopropyl phenols, and US Pat. No. 3,386,955, showing urea derivatives such as toluene-2,4-bis- (N, H-dimethylurea> A suitable latent hardener is 4,4'-diaminodiphenyl sulfide. Especially dicyandialdehyde. The mixture of the present invention may also contain an accelerator for complexing reaction with the latent hardener. Agent (e). Examples of suitable accelerators (e) are hemp derivatives such as ^ -dimethyl-^ '-(3-gas-4-tolyl) screen (gas toluene), 1 ^'-dimethyl -N '-(4-Phenylphenyl) -P (monosaccharide aldehyde) or Ν, Ν'-dimethyl-H'-(3,4-dicyanophenyl) diurea (bis aldehyde), 2 , 4-Bis- (Ν, Ν'-dimethylsulfonyl) -toluene or 1,4-bis-U ', Ν'-dimethylureido) -benzene. These compounds used are shown in the above-mentioned U.S. Patent 4,283,520. In addition, the urea derivative contained in US Patent 1,192,790 is also a suitable accelerator (please read the precautions on the back before filling out this page) • Order. Printed by the Ministry of Economic Affairs Central Standards Bureau $ !. 1- 1, cyanocyanine, -4-based or oxazolyl ammonium ammonium 4-ethyl 2-ammonium, bromobenzene or quaternary phenol-up-t 2¾ or}, cyanotriazole-based Ethylbenzyl methyl- or 4-aminoamines. Amine methylation 2-w_ three 1 one M, -z into the first-(the base of the oxazol-2 to promote the trimethyl squint group 6-four as ethyl when into 4, 4, for example, cyanogen promote 2, salt, 1- for , Phenols, ammonium, oxazolazole, toluene, succinimide and bistriyl benzene, .Line · A 4 (210X 297 public release) 5. Description of the invention (8 A6 B6 ammonium; alkali metal alkoxide, such as 2,4 -dihydro-3-hydroxymethyl compound sodium alkoxide. Krypton solid solution and phenol / aldehyde resin contained in EP-A200,678, and polymerized phenol shown in EP-A351,365 Class Mannich (Mannich) is also a suitable accelerator. The best accelerator (e) is azoles or hemp derivatives. As mentioned, the amine component (c) of the mixture of the present invention is at least Any amine with an amine hydrogen. To obtain good results, the amine (c) or thiol (d) must contain at least three slap hydrogen atoms that are active on the ring gas resin. For amine strips, only 0 Ziyuan 0 two less than the need to combine the situation, the first situation is to use PC containing amines. The use of all amines and any use of the original results in a amine ring heterocyclic and aromatic aromatic alicyclic. Lipogen is Example three suitable or} bis (C category, amine diamine N, such as octane,, n-pentylamino, 3 benzene T aminoethane 4-propane methylamine diamine dimethyl hexamethylene {please read first Note on the back and then fill out this page). Therefore. I 2 RM »tree-1 0 methyl methyl / aminobenzene diamine triene ethylamine benzyl new yfv amine dipropyl propylamine pentene ethylene tetramine tetraene ethylene Triamine methyl! \ 1 / propylpropylamine, and amine 2-hexyl 1, ene, ethylamine glutaryl, ylaminobenzene-alkanehexylcycloethyltriamine 4-one-amine. Order. Diamine methylhexyl Bicyclo-yl. Line. Dialkylmethane-\ — / Alkylamine and alkylpropyl-ylhexylcycloamino: Hexane? Cyclomethine 3 Limbrane diisopropyl / IV Amine Cyclomethine Central Standard of the Ministry of Economy Local printing of oxazolidine amine polydihexylamine), family amine lipid two by ketol Kolverfo compound and this is for example amine 0 amine amine polyamine suitable 0 to obtain fatty acid lipid body A 4 ( 210〆297 Public Issue) A6 B6 V. Description of the invention (9) (c) Polyalkylene amines, known by Jeffa ^ ines® produced by Texaco, such as Jeffanines® E0R148. D230, D400 or T403o and suitable amines are 1,14-diamino-4,11-dioxadecane, dipropylene triamine, 2-methyl-1,5-pentanediamine, Ν, Ν '-Diethylhexyl-1,6-hexanediamine, Ν, Ν'-dimethyl-1,3-diaminopropane, Ν'-diethyl-1,3-diaminopropane, Ν, Ν-dimethyl-1,3-diaminopropane, second polypropene diamines and triamines, such as EPS7315 and EPS7325 produced by Texaco, 2,5-diamino-2,5-di Methylhexane, bis- (aminomethyl) -tricyclopentadiene, m-aminobenzylamine, 1,8-diamino-p-methane, bis_ (4-amino-3,5-di Methylcyclohexyl) -methane, 1,3-bis- (aminomethyl) -cyclohexane, dipentylamine, bis- (4-amino-3,5-diethylphenyl) -methane, 3, 5-Diethyltoluene-2,4-diamine and 3,5-diethyltoluene-2,6-diamine (Please read the precautions on the t side before filling out this page) -Subscribe. Make W 0 items The oil diglycerin is less water and shrinks to be the best one with special envoys. There are amine minorities to Zhiyi and} ethnic groups. (c Lipid-based cyclic amine groups are made of pseudo-lipids, such as the group of tree-based components, which is suitable for the most suitable mixed amine aliphatic lipids or family § β-ring is. The line is suitable for those with the most Among them, the ® class Γ amine du group ΓΟ fat E ring 0 is sold in the market, which is printed by the example of the alkylhexyl amine di AG methyl group in the Central Ministry of Economics and Trade of the Ministry of Economic Affairs. Hexacyclomethyl trisylidene compound), the amine VI di or ketone I Erfuroline isoxazole νίν succinylamine poly and alkylmethylamine methyl 4 (210X 297 Koji) V. Description of the invention (10) A6 B6 H2N-R-NH2 (I), H2N ~ (-CH2CH20) aCH2CH2NH2 (Π), CH3 CH,

經濟部中央標準局印裝 H2N(CH2CH2CH2NH)fCH2CH2CH2NH2 (V), H2N(CH2CH2NH)gCH2CH2NH2 (VI), 其中1^為直鰱或分枝之C2-CW烷撐基画,a為1至 10之整數,最好為2 , b為1至10之整數,宜為2至6, c,d和e偽各自描立為1至20之整數,最好為2至5 , f 為1至5之整數,宜為1 ,而g為1至10,最好為1至 CH 2~ I 5 ,而!?!為式 CH- 之三價基團或待別為CH3CH2C I CH 2~ ,最好偽在脂族胺(c)之中間。 式]I 之 Jeffanine® EDR148.即 2,2,2-三甲基己烷-1, 6 -二胺其中 a = 2,式 Ϊ 之 Jeffaminee® D230 或 D400其中 b =2 - 3 或 b = 5 - 6 ,式 IV 之 J e f f a m i n e e β T 4 0 3 ,即雙-(3- 胺丙基)-胺,二乙烯三胺,三乙烯四胺,2,2 -二甲基-1 , 3 -丙二胺和戊乙烯己胺係待別適用。 最適用之胺類為正辛胺,4,4’-二胺基二瓖己基甲烷, Teffanine® EDR 1 48 , Laromin ® C - 260 , (BASF, 3,3'- 12 (請先閱讀背面之注意事項再填寫本頁) 甲 4(210X 297公廣) 經濟部中央標準局印裝 (ονϋΊά α6 * Β6 五、發明說明(11) 二甲基-4,4'-二胺基二琛己甲烷),1,2 -二肢基己烷和 異佛爾酮二胺。 在絡接之第一階段胺(c)和硫酵(d)係一起做為硬化 劑使用。一般至少具有一傾而最好為二餾或三嫡SH基之 任何適當之化合物均可做為硫醇(d)使用。硫醇之適例 為三乙二醇二硫醇或1,2 -雙- (2’-兢乙氣基)-乙烷,如式 HS(CHZ CH2 OCHz OCHz CHz SS)n CHz CHz 〇CHz OCHz CHZ S 以Thiokols®為名稱之聚合的聚硫醚,三甲醇丙烷三硫 乙二醇鹽及其他之硫代乙二醇鹽,例如美國專利 3,352,810所掲載之化合物,掲示於美國專利3, 716, 588 ,3,734,968, 3,718,700 和 3,278,496之脂族及環脂族 二硫醇類型,美國專利3,310,527所掲載之聚-(覲烷基) 芳族化合物,美國專利3,363,026所記載之烷撺二硫醇 類或羥烷撺二硫醇類,季戊四醇六-(3-兢基丙酸鹽), 單硫醇如鲸蠟基硫醇,苄基硫醇,戊基硫醇,己基硫醇 ,辛基硫醇或癸基硫醇或三硫醇類如2,4,6-S-三嗪三硫 醇。 適宜之硫醇為聚氧烷撺衍生物類,特別是聚氧烷撺_ 二硫醇類或-三硫醇類。 例如該些硫醇可為聚乙二醇衍生物,聚丙二醇衍生物 或為包含氧乙烯單位或氣丙烯單位之共聚物。此共聚物 乃為分段聚合物或無規聚合物。相關之分段聚合物有時 亦稱做為聚丙二醇羥乙酯或聚乙二醇羥丙酯,其傜以所 -1 3 - (請先閲讀背面之注意事項再填寫本頁) •蛑· .訂· •線 甲 4(210X 297父发) A6 ^_ 五、發明説明(12 ) 具有之末端聚乙二醇分段或聚丙二醇分段而定。商用之 聚丙二醇主要者具有第二末端羥基;當然己知之具有第 . 一硫醇基之聚丙烯二醇亦可使用。 其他適用之二硫醇傜衍自聚四氫呋喃二醇類。聚四氳 呋喃二醇類偽屬習知亦為商業级産品。該些生成物之實 例為由 BASF所産製之 poly-THF 650®, P〇ly-THF1000e P〇ly-THF2000®。該些商業上可資利用之二醇類,例如 偽藉由與亞硫醛氮反應可轉換為二氱代衍生物,其像與 硫脲反應得相鼷之異氣化硫胨,然後將此生成物水解成 二硫醇。醇類轉換為硫酵在Organic Synthesis, Collective Volume 3, pp698-700 以及 Collective Volueie 4 pp 401-433, wiley, New Yook, 1955和 1963有詳細 之解說。 適當之硫醇(d)傷以 CapCuree(Henkel Hapco AG)所 出售之聚氣烷撐衍生物,例如CapCure® V/R-6或VR-36, 特別是式 R-KHOHjHCHirCHIHCI^SHh 之 CapCure® ,H2N (CH2CH2CH2NH) fCH2CH2CH2NH2 (V), H2N (CH2CH2NH) gCH2CH2NH2 (VI) printed by the Central Bureau of Standards of the Ministry of Economic Affairs, where 1 ^ is a straight or branched C2-CW alkylene base painting, a is an integer from 1 to 10 , Preferably 2, b is an integer from 1 to 10, preferably 2 to 6, c, d and e are each described as an integer from 1 to 20, preferably from 2 to 5, f is an integer from 1 to 5 , Should be 1, and g is 1 to 10, preferably 1 to CH 2 ~ I 5, and! ? ! It is a trivalent group of formula CH- or may be CH3CH2C I CH 2 ~, preferably in the middle of the aliphatic amine (c). Formula] Jeffanine® EDR148 of I. That is 2,2,2-trimethylhexane-1,6-diamine where a = 2, Jeffaminee® D230 or D400 of formula Ϊ where b = 2-3 or b = 5 -6, J effaminee β T 4 0 3 of formula IV, namely bis- (3-aminopropyl) -amine, diethylenetriamine, triethylenetetramine, 2,2-dimethyl-1,3-propane Diamine and pentamethylene hexylamine are to be applied separately. The most suitable amines are n-octylamine, 4,4'-diaminodioxanyl methane, Teffanine® EDR 1 48, Laromin ® C-260, (BASF, 3,3'- 12 (please read the back (Notes and then fill out this page) A4 (210X 297 Public Broadcasting) Printed by the Central Bureau of Standards of the Ministry of Economic Affairs (ονϋΊά α6 * Β6 V. Description of the invention (11) Dimethyl-4,4'-diaminodichen hexanemethane ), 1,2-dimeryl hexane and isophorone diamine. In the first stage of complexing, amine (c) and thiol (d) are used together as a hardener. Generally, at least one Any suitable compound that is preferably a distillate or tri-SH group can be used as the thiol (d). A suitable example of the thiol is triethylene glycol dithiol or 1,2-bis- (2'- Ethane gas) -ethane, such as the formula HS (CHZ CH2 OCHz OCHz CHz SS) n CHz CHz 〇CHz OCHz CHZ S polymerized polysulfide under the name Thiokols®, trimethanol propane trithioglycol salt and Other thioglycol salts, such as the compounds contained in U.S. Patent 3,352,810, are shown in U.S. Patent Nos. 3,716,588,3,734,968, 3,718,700, and 3,278,496 for aliphatic and cycloaliphatic dithiols. Poly- (Alkanoyl) aromatic compounds contained in 3,310,527, alkane dithiols or hydroxyalkane dithiols described in US Patent 3,363,026, pentaerythritol hexa- (3-amylpropionate), Monomercaptans such as cetyl mercaptan, benzyl mercaptan, pentyl mercaptan, hexyl mercaptan, octyl mercaptan or decyl mercaptan or trithiols such as 2,4,6-S-triazine tris Mercaptan. Suitable thiols are polyoxyalkylene derivatives, especially polyoxyalkylene dithiols or trithiols. For example, these thiols can be polyethylene glycol derivatives, polypropylene glycol The derivative may be a copolymer containing oxyethylene units or propylene units. This copolymer is a segmented polymer or a random polymer. The related segmented polymers are sometimes referred to as polypropylene glycol hydroxyethyl or polymer Ethylene glycol hydroxypropyl ester, its 傜 以 所 -1 3-(Please read the precautions on the back before filling in this page) • Insect · · Order · • Line armor 4 (210X 297 father hair) A6 ^ _ V. Invention The description (12) depends on the terminal polyethylene glycol segment or polypropylene glycol segment. Commercially available polypropylene glycol mainly has a second terminal hydroxyl group; of course, it is known that it has the first. Polythiol-based polypropylene glycol can also be used. Other suitable dithiols are derived from polytetrahydrofurandiols. Polytetrahydrofurandiols are also known as commercial grade products. The products of these products Examples are poly-THF 650®, P〇ly-THF1000e P〇ly-THF2000® produced by BASF. These commercially available diols, for example, can be converted into dihydric derivatives by reacting with thionaldehyde nitrogen, which reacts with thiourea to produce a different gaseous isopeptide, and then The product is hydrolyzed to dithiol. The conversion of alcohols to sulfur enzymes is explained in detail in Organic Synthesis, Collective Volume 3, pp698-700 and Collective Volueie 4 pp 401-433, Wiley, New Yook, 1955 and 1963. Appropriate thiols (d) injure polyalkylene derivatives sold by CapCuree (Henkel Hapco AG), such as CapCure® V / R-6 or VR-36, especially CapCure® of formula R-KHOHjHCHirCHIHCI ^ SHh,

CH3 OH 其中n = l- 2而R為脂族烴之三價基圃。 特別適宜之二硫醇為式HS(CHz CH2 〇 4m Η 2 C Η 2 S Η 以及 HS(CH2 CHz CHz CH2 0 4τττ~ε Η 2 CHz CH2 CHz SH 之 Μ 化合物其中πι = 7- 8, 12-13或26-27。 經濟部中央標準局印裂 (請先閲讀背面之注竟事項再填寫本頁) .訂. .線. 最為適用者為三乙二醇二硫醇,CapCure® 3-800和三 甲酵丙烷三硫乙醇酸鹽。 -14-甲 4(210X 297 公发) A6 B6 — 五、發明說明(13) 適合者,乃為本發明之混合物亦可含有胺/硫醇硬化 用促進剤,例如酚類,如壬基酚或間苯雙酚,或有機酸 類如對甲苯磺酸。 本發明混合物組成份之用量比率至為廣泛偽以特定之 組成份而定。潛硬化劑之適宜用置,例如僳在約3至60 之範圍,最好為依環氣樹脂100份重為計,其用量為約 6至30份重。 如於B製造階段,通常該些混合物含有約5至50SS, 尤其是約10-35X之樹脂環氣基俗由胺/硫醇混合物所絡 接,而殘餘之環氣基俗由潛硬化劑所硬化。 NH基/ SH基之當量比亦極為廣泛,視所使用硫酵或胺 以及B階段所需特性而定。例如NH/SH當量比為約15:1 至1:6,而最具適合者乃為約10:1至約1:3。 組份(c)和(d)之使用量像依照應用設計而定,即視B 階段所需要之可撓性以及混合物之所需使用壽命而做適 度之增減。通常,如增加可撓性及使用赛命時,在硫醇 /胺混合物中硫酵之使用量亦獲增加。 促進劑(e>之用量,可添加促使潛硬化劑(b)産生硬化 或添加加促進劑使胺(e)和硫醇(d)硬化,蓋此一般熟習 於此項技藝人士可随意使用任何類型之促進劑。 本發明混合物餾別組份適當用量之例子可參照具體實 (請先閱讀t面之注意事項再填寫本頁) .襄· • ΛΤΤ· .線.CH3 OH where n = l-2 and R is a trivalent base of aliphatic hydrocarbons. Particularly suitable dithiols are compounds of the formula HS (CHz CH2 〇4m Η 2 C Η 2 S Η and HS (CH2 CHz CHz CH2 0 4τττ ~ ε Η 2 CHz CH2 CHz SH π compound = 7- 8, 12- 13 or 26-27. The Central Bureau of Standards of the Ministry of Economic Affairs has cracked (please read the notes on the back and then fill out this page). Order .. Line. The most suitable is triethylene glycol dithiol, CapCure® 3-800 And trimethyl enzyme propane trithioglycolate. -14-A 4 (210X 297 public) A6 B6 — V. Description of the invention (13) Suitable for the mixture of the present invention may also contain amine / mercaptan hardening accelerator For example, phenols, such as nonylphenol or resorcinol, or organic acids, such as p-toluenesulfonic acid. The ratio of the components of the mixture of the present invention is determined by the specific components to be widely pseudo. The latent hardener is suitable Use, for example, in the range of about 3 to 60, preferably based on 100 parts by weight of the ring gas resin, the amount is about 6 to 30 parts by weight. As in the manufacturing stage of B, usually these mixtures contain about 5 to 50SS, especially about 10-35X resin ring gas base is connected by amine / mercaptan mixture, and the remaining ring gas base is made by latent hardener Hardening. The equivalent ratio of NH group / SH group is also very wide, depending on the thiol or amine used and the required characteristics of stage B. For example, the NH / SH equivalent ratio is about 15: 1 to 1: 6, which is the most suitable It is about 10: 1 to about 1: 3. The usage of components (c) and (d) is determined according to the application design, that is, depending on the flexibility required for the B stage and the required service life of the mixture Do a moderate increase or decrease. Generally, if you increase flexibility and use the game, the amount of thiol in the thiol / amine mixture is also increased. The amount of accelerator (e > can be added to promote the latent hardener ( b) Produce hardening or add an accelerator to harden the amine (e) and thiol (d), and those skilled in the art can use any type of accelerator at will. The proper amount of the mixture fraction of the invention For examples, please refer to the specific facts (please read the precautions on the t side before filling out this page). Xiang · • ΛΤΤ ·.

經濟卸中央標準局印$L 乙改 甲無 在並 如化 例硬 ,段 造階 製 C 以以 加度 液溫 溶用 。由化 解可硬 瞭物段 加合階 更混 B 能之中 當明其 份發 , 成本行 組照進 例依中 施酮 甲 4(210X 297公; A6 B6 五、發明説明(14) 變。 如有痛要時,可將反應性稀釋劑,例如丁二醇二縮水 甘油醚,異構化高级酵類之單縮水甘油醚,例如Grilonit RV 1814* (Ens-Chedce公司産品),或丁縮水甘油醚, 2,2,4-三甲苯基縮水甘油醴,苯基縮水甘油醚,甲苯基 縮水甘油醚或縮水甘油酯均可加入於可硬化混合物以減 少黏度。 本發明混合物亦含有黏着促進_,原則上任何已知之 黏着促進剤皆能使用。矽烷類,例如7-缩水甘油氣丙 基三甲氣矽烷(U n i ο n C a r b i d e e公司産製之S i 1 a n e A - 1 8 7 ) 或γ -醯丙基三甲氣矽烷(Union Carbidee公司産製之 Silane A-189)或鈦化合物如四異丙基雙-(二辛瞵酸基) -欽酸酷(美國Kenrich Petrochenicals公司産製之KR 41B)已證實特別適宜之一種黏着促進_。 經濟部中央標準局印製 (請先閲讀背面之注意事項再填寫本頁) •訂· _線_ 鼷於其他習知之添加物,本發明混合物亦可包含有增 充劑,媾充劑及強化例如煙煤焦油,瀝育,嫌物鐵 維,玻瑱纖維,石棉鑛維,硼纖維,硪纖維,礦物矽酸 鹽,雲母,石英粉末,水合二氣化鋁,膨潤土,矽灰石 ,高嶺土,矽氣凝膠或金颶粉末,例如鋁粉或鐵粉,以 及顔料和染料,如硝黑,氣化物顔料和二氣化鈦,防火 劑,觭變劑,流量控制劑如矽嗣類,石蠟類和硬脂酸鹽 ,其中之某些物質偽可作為脱模劑,抗氣化劑和光安定 劑使用。 , -16-甲 4(210X 297公沒) ,,·*) f ^01 r- - A6 _B6 五、發明説明(15) 本發明混合物傜由習知方法利用既有之混合設備(掇 拌器,滾筒機)將組成份混合加以製備。 本發明混合物,例如可做為黏着劑(黏着薄膜,熱熔 化物,膠漿,單一組份黏着劑,金鼷片),架陣樹脂類 ,表面塗料,封閉化合物或射出化合物,或通常之製造 硬化生成物使用。在毎一情況所使用之配方刖應用於無 琪充或填充狀態下之不同領域,例如作為密封化合物, 油漆,塗料組成物,尾工料,浸製樹脂,澆薄樹脂,尤 其是預浸樹脂,層製樹脂,架陣樹脂及黏着劑使用。 是以本發明亦有關於一種絡接産品俗將本發明混合物 經由硬化而獲得。 混合物之硬化宜在約80-18010之溫度範圍下進行。與 胺/硫醇硬化劑完成硬化反應後,例如在9〇-12〇υ硬化 約2-10分鐘,可得儲存安定,非臨界Β階段条並顯示有 優異可撓性和膠黏性産品。具有塑型之完全絡接作用宜 在約100-1801下進行約20-60分鐘。 絡接糸縱然將可硬化混合物經由長久儲存(幾星期至 幾倨月)或於Β階段進行完全硬化亦具有優異之機械強 (請先聞讀背面之注意事項再填寫本頁) .訂· 經濟部中央標準局印焚‘ 維將合 纖可混脂 備種於樹 製一漬氣 為於浸環 作關維至 於亦纖直 用明使熱 適發,加 別本物維 特以合纖 物是混之 合。之潰 混用明浸 之使發將 明脂本即 發樹於随 。本漬潰 , 性,預浸體 特述之.體漬 照所材漬預 耐上體預得 及如合維獲 度複纖而 ,線· 甲 4(210Χ 297 公犮) -ΟΐΙΊά Α6 ^_ Β6_ 五、發明説明(16) (a)與胺(c)和硫醇(d)之反應完成為止,不同時使環氧 樹脂(a)與潛硬化劑(b)開始反應,因預潰體完成硬化而 獲得層製品。 再者,本發明之混合物可做為黏着劑使用,待別是熱 熔化反應性鈷着薄I和黏着薄膜。在25〜501C溫度形成B 階段後獲得儲存安定性之黏着劑醪糊,在製程中可添加 或不添加《充劑。黏着的黏度經由B階段程度時則呈不 同。 以下實施例俗舉例說明本發明。 奮施例1-11 下列組成份偽使用於表1中所界定之組成物: 環氛樹脂1 :具有186.2克環氣化物當置之雙酚A二縮水甘 油醚。 m mm m 2:具有235克環氧化物當量之琛氧甲酚酚醛清漆。 摄氛樹脂3 :具有380克環氧化物當置之固體雙酚a樹脂。 潜硬化割1 : 2 5 . 2份東之二氰二醅胺,12. 5份重之氱甲苯 (^),1二甲基-{<’-(3-氣-4-甲苯基)-麻],46.5份重之具 有192.3克環氣化物當量之雙酚A二縮水甘油醚及15.5 份重之具有222.2克環氣化物當量之雙酚A二縮水甘油 醚之混合物。 經濟部中央標準局印"- (請先閱讀背面之注意事項再填寫本頁) *打· •線. 潜硬化酬2 : 28份重之二氡二醛胺及72份重之具有192.3克 環氧化物當量之雙酚A二縮水甘油《之混合物。 潜確化酬3 : 4,4'-二胺基二苯基亞楓。 -18-甲 4(210>' 297 公发) 經濟部中央標準局印製 汕1的 五、發明説明(17) 將所有組成物混合,如有需要時稍加熱以製備組成物 〇 清艚(PP)和靥餺品夕魁備:將由Interglas所製造之玻璃 纖維(92146-1-550)(43X 25c»)在50TC下浸潰於具有黏 合劑混合物之片材上。除去空氣並將黏合劑均勻分佈, 將玻璃棒滾壓在預漬體上。到逹Β階段,使每一預漬體 在9 0 - 1 2 0 之熱板上加熱2 - 1 0分鐘(如表2 )。製造層製 品,將預漬體裁切成等規格之片材(6.5X9.9cm)。除去 片才,將12層叠合,於最高為5MPa之壓力下經由模型加 壓成形並在適當之溫度加以硬化。層製品之厚度為3-3.3 mm。切割所形成層製品作為試樣計算其内層之抗剪強度 〇 利用由英國劍橋Tec hne公司製造之Techne Gelation T i m e「G T 3測計在5 0 之嘐凝時間(參照表3 )。在1 2 0 之膠凝時間即由自動性之膠凝時間熱板加以測定。線布 條(直徑0.4ιπβ)偽將實物拉引直到後者到逹所界定之固 體化為止。 利用瑞士 Dottikon Epprecht工具公司所製造之ICI 錐形和平板黏度計測定其黏度。 使用Mettler TA3000熱分析糸進行計算DSC和Tg。 A6 B6 (請先閏讀背面之注意事項再填寫本頁) •襄. ,訂. .線. 甲 4(210X ‘297 公发) L01773 A6 B6 五、發明説明(17a) 宑1 :甜成物:> 嫌成》其執行為 UH2 N-(CH2 CH2 0)2 CH2 CH2 HH2 由 Texco 産製 2 ) 由 Η鎮 enkel Hapco公司産製 3)由DSC測定(使用Metller TA 3000:加熱速率1〇υ/ 分)。 實施例编號 璟氣化物樹脂1 (克) ......................................................It..............................^...................................^ (請先閲讀背面之注意事項再填寫本買) 經濟部中央標準局印裝 甲 4 (210X297公遵) A6 B6 經濟部中央標準局印製 五、發明説明(18) 丟1:绀成物;> 縑成》其執行為 實例编號 1 2 3 4 5 環氣樹脂1 (克) 70 70 80 80 80 環氣樹脂2 (克) 30 30 環氣樹脂3 (克) 20 20 20 潛硬化劑1(克) 37.3 31.5 34.8 33.8 33.3 η-辛基胺(克) 2.5 異彿爾酮二胺(克> 2.63 4, 4’-二胺基-二環己 2.9 基甲烷(克) Jeffamine® EDR- 2.4 1 48 1 (克) 1,2-二肢基環己院(克) 2.1 三乙二醇二硫醇(克) CapCure ® 3 -800 2 (克) 4.3 5.6 2.82 2.8 2.8 B Stage m a x ("C ) 3 94 102 85 93 91 c Stage mQx (X) ) 3 146 147 147 146 146 — 20 - (請先閱讀背面之注意事項再填寫本頁) 甲 4(210X 297 公发) .襄. .訂. .線The Economic Discharge Central Standards Bureau prints $ L. B is changed to A. It is absent and hardened as usual, and a stage C is used to dissolve it at an increased liquid temperature. By dissolving the hardening stage, the addition stage is more mixed, and the energy can be clearly distributed. The cost line group is routinely administered with ketone methyl 4 (210X 297 g; A6 B6 V. Invention description (14). In case of pain, reactive diluents such as butanediol diglycidyl ether, isomerized high-enzyme monoglycidyl ether, such as Grilonit RV 1814 * (Ens-Chedce company product), or butyl glycerol Glycerol ether, 2,2,4-tritolyl glycidyl alcohol, phenyl glycidyl ether, tolyl glycidyl ether or glycidyl ester can be added to the hardenable mixture to reduce the viscosity. The mixture of the present invention also contains adhesion promotion_ , In principle, any known adhesion promoter can be used. Silanes, such as 7-glycidyl gas propyl trimethyl gas silane (U ni ο n C arbidee company produced S i 1 ane A-1 8 7) or γ -Acetyltrimethylsilane (Silane A-189 manufactured by Union Carbidee) or titanium compounds such as tetraisopropylbis- (dioctanoic acid)-Qin acid cooler (KR 41B manufactured by Kenrich Petrochenicals, USA) ) Has proved to be particularly suitable for an adhesion promotion _. Printed by the Central Bureau of Standards (please read the precautions on the back before filling in this page) • Order · _LINE_ in other conventional additives, the mixture of the present invention may also contain extenders, fillers and reinforcements such as Bituminous coal tar, leach, skeletal iron, glass fiber, asbestos mineral, boron fiber, fiber, mineral silicate, mica, quartz powder, hydrated aluminum oxide, bentonite, wollastonite, kaolin, silicon Aerogel or gold powder, such as aluminum powder or iron powder, as well as pigments and dyes, such as nitric black, vaporized pigments and titanium dioxide, fire retardants, altering agents, flow control agents such as silicon and paraffin And stearate, some of which can be used as a mold release agent, anti-gasification agent and light stabilizer., -16-A 4 (210X 297 public) ,, *) f ^ 01 r-- A6 _B6 V. Description of the invention (15) The mixture of the present invention is prepared by mixing the components by conventional methods using the existing mixing equipment (mixer, drum machine). The mixture of the present invention can be used as an adhesive (adhesive film, hot melt, glue, single-component adhesive, gold foil, for example), matrix resins, surface coatings, sealing compounds or injection compounds, or generally manufactured Use of hardened products. The formula used in each case is used in different fields without filling or filling, for example, as a sealing compound, paint, coating composition, finishing material, impregnating resin, thin casting resin, especially prepreg resin, Layered resin, frame resin and adhesives are used. Therefore, the present invention also relates to a conjugated product which is obtained by hardening the mixture of the present invention. The hardening of the mixture is preferably carried out in a temperature range of about 80-18010. After completing the hardening reaction with the amine / mercaptan hardener, for example, hardening at 90-12 ° C for about 2-10 minutes, a stable storage, non-critical B-stage bar is obtained and the product exhibits excellent flexibility and adhesiveness. The complete complexing function with shaping is preferably carried out at about 100-1801 for about 20-60 minutes. Even if the hardenable mixture is stored for a long time (a few weeks to several months) or is completely hardened in the B stage, it has excellent mechanical strength (please read the precautions on the back and fill in this page). Ministry of Central Bureau of Standards 'Printing and Burning' dimensional preparation of synthetic fiber blendable fat in a tree to make a stain for the dip ring as a maintenance dimension, as well as straightening the hair to make the heat suitable for hair, plus the original material Vit is mixed with synthetic fiber Fit together. The collapse of the mixed use of the Ming Baptist made the hair fat appear on the tree. This stain, sex, prepreg is described in particular. Body stains are based on the material stains pre-preserved by the upper body and are obtained as a multidimensional fiber, thread · A 4 (210Χ 297 Gonglu)-ΟΐΙΊά Α6 ^ _ Β6_ V. Description of the invention (16) (a) When the reaction between the amine (c) and the thiol (d) is completed, the epoxy resin (a) and the latent hardener (b) are not reacted at the same time due to the pre-collapse Complete hardening to obtain laminates. Furthermore, the mixture of the present invention can be used as an adhesive, except for the thermal melting of reactive cobalt thin I and adhesive films. After forming the B stage at a temperature of 25 ~ 501C, the storage stability of the adhesive mash can be obtained. The filler can be added or not added during the process. The viscosity of adhesion varies with the degree of B stage. The following examples illustrate the invention. Examples 1-11 The following components were pseudo-used in the composition defined in Table 1: Ambient Resin 1: Bisphenol A diglycidyl ether with 186.2 grams of cyclic gaseous substance in place. m mm m 2: oxycresol novolac with 235 g epoxide equivalent. Atmosphere resin 3: Solid bisphenol a resin with 380 grams of epoxy resin. Latent hardening cut 1: 2 5. 2 parts of dicyandiamide, 12.5 parts of methyl toluene (^), 1 dimethyl-{< '-(3-gas-4-tolyl) -Hemp], a mixture of 46.5 parts by weight of bisphenol A diglycidyl ether having a ring gas equivalent of 192.3 grams and 15.5 parts by weight of bisphenol A diglycidyl ether having a ring gas equivalent of 222.2 grams. Printed by the Central Bureau of Standards of the Ministry of Economic Affairs "-(please read the precautions on the back before filling in this page) * Take a line • Latent hardening remuneration 2: 28 parts by weight of radon dialdehyde amine and 72 parts by weight with 192.3 grams Epoxy equivalent of a mixture of bisphenol A diglycidol. Potentially confirmed remuneration 3: 4,4'-diaminodiphenylyafeng. -18-A4 (210 > '297 Public Issue) Fifth, invention description printed by Shan 1 of the Central Standards Bureau of the Ministry of Economic Affairs (17) Mix all the components and heat them slightly if necessary to prepare the composition. PP) and high-quality products: prepare glass fiber (92146-1-550) (43X 25c ») manufactured by Interglas at 50TC on a sheet with a binder mixture. Remove the air and distribute the adhesive evenly. Roll the glass rod onto the pre-stain. To the B-stage, each pre-stained body is heated on a hot plate of 90 to 120 for 2 to 10 minutes (see Table 2). Manufacture the layered product, and cut the pre-stained body into equal-sized sheets (6.5X9.9cm). After removing the sheet, the 12 layers are laminated and pressed under a pressure of up to 5 MPa through the mold and hardened at an appropriate temperature. The thickness of the laminate is 3-3.3 mm. Cut the layered product as a sample to calculate the shear strength of the inner layer. Use the Techne Gelation Time "GT 3" manufactured by Tec Hne of Cambridge, England at a gel time of 50 (refer to Table 3). In 1 2 The gel time of 0 is measured by the automatic gel time hot plate. The wire strip (diameter 0.4ιπβ) pseudo-pulls the object until the latter reaches the solidification defined by Y. Manufactured by Swiss Dottikon Epprecht Tool Company ICI cone and plate viscometer to measure its viscosity. Use Mettler TA3000 thermal analysis to calculate DSC and Tg. A6 B6 (please read the notes on the back before filling this page) • Xiang. 4 (210X '297 public) L01773 A6 B6 V. Description of the invention (17a) Mi 1: Sweet product: > suspected "It is executed as UH2 N- (CH2 CH2 0) 2 CH2 CH2 HH2 produced by Texco 2 ) Manufactured by Enkel Hapco, H Town 3) Measured by DSC (using Metller TA 3000: heating rate 1〇υ / min). Example number Jing gasified resin 1 (g) ... ............................................. It ... .......................... ^ ... .......................... ^ (Please read the precautions on the back before filling in the purchase) Ministry of Economic Affairs Central Standards Bureau Printed Armor 4 (210X297 official compliance) A6 B6 Printed by the Central Bureau of Standards of the Ministry of Economy V. Description of Invention (18) Throw 1: Cyan Cheng; > Xuan Cheng "is executed as example number 1 2 3 4 5 Resin 1 (g) 70 70 80 80 80 Ring gas resin 2 (g) 30 30 Ring gas resin 3 (g) 20 20 20 Latent hardener 1 (g) 37.3 31.5 34.8 33.8 33.3 η-octylamine (g) 2.5 Isophorone diamine (g > 2.63 4, 4'-diamino-dicyclohexyl 2.9 methane (g) Jeffamine® EDR- 2.4 1 48 1 (g) 1,2-dimeryl cyclohexylamine (G) 2.1 Triethylene glycol dithiol (g) CapCure ® 3 -800 2 (g) 4.3 5.6 2.82 2.8 2.8 B Stage max (" C) 3 94 102 85 93 91 c Stage mQx (X)) 3 146 147 147 146 146 — 20-(please read the precautions on the back before filling in this page) A4 (210X 297 public). Xiang ... Order ... Line

Oim A6 B6 五、發明説明(19) ” H2N~eCH2CH20)2CH2CH2NH2 由Texco産製 2)R-Oim A6 B6 5. Description of the invention (19) ”H2N ~ eCH2CH20) 2CH2CH2NH2 produced by Texco 2) R-

-〇tCH2CHO)i3-CH2CHCH2SH CH3 OH 由Henke丨Napco公司産製 3)由DSC測定(使用Mettler ΤΑ 3000;加熱速率IOC 分)ο (請先閱讀背面之注意事項再填寫本頁) •装· •訂. •線_ 經濟部中央標準局印裂 甲 4(21〇X 297W发) 3 νί 4ax ο-〇tCH2CHO) i3-CH2CHCH2SH CH3 OH manufactured by Henke 丨 Napco 3) Determined by DSC (using Mettler ΤΑ 3000; heating rate IOC points) ο (please read the precautions on the back before filling in this page) • Installed • Order. • LINE_ The Central Standards Bureau of the Ministry of Economic Affairs Printed Split Armor 4 (21〇X 297W issued) 3 νί 4ax ο

A B 五、發明説明(20) 實施例编號 6 7 8 9 10 11 環氧化物樹脂1(克) 100 100 100 100 70 100 環氣化物樹脂2 (克) 30 潛硬化劑1(克) 35.1 潛硬化劑2(克) 38 潛硬化劑3(克) 32.9 27.4 6 2,4-燹-(Ν,Ν'-二甲 基脲)-甲苯(克) 6 1,4-雙-(Ν,Ν’-二甲 基脲)-苯(克) 6 1-苯醛基-2-異丙基 咪唑(克) 2.3 1-(2· ,4' ,6,-三甲苯 _ 基)-2-苯基眯唑(克) 3 1-氳乙基-2-乙基-4-甲 基咪唑(克) 1.7 異氟爾_二胺(克) 2.1 2.3 2 2.75 2 2.33 CapCure ® 3-800 5.4 三乙二醇二硫醇 5.8 7 4 7 三中醇丙烷三硫乙醇酸 鹽 7.3 b階段最大(υ ) 68 86 102 128 127 97 c階段最大(υ ) 133 143 151 162 171 159 (請先閲讀背面之注意事項再填寫本頁) .装. •訂· .線_ 經濟部中央捃準局印裂 甲 4(210X 297公发) 五、發明説明(21) A6 B6 表2 :預清體(PP):>苕逋右宙杜 實施例鏞號 之組成物 ΡΡ製備1 分/它 及至X 高 天時= 中 ^睡黏性 低 及至X天爸 很好 &之可擒性 尚佳 1 10/100 11 15 16 11 15 2 10/100 - 30 45 48 58 5/110 - 30 45 45 50 3/120 - 30 45 40 45 3 5/110 17 24 30 20 30 4 5/110 14 19 22 14 22 5 5/110 10 20 22 14 22 6 5/110 7 10 14 7 12 7 5/90 3 6 7 3 7 8 5/100 1 7 18 7 18 9 5/110 5 20 26 20 26 4/120 5 12 18 12 18 10 5/100 — 10 16 10 16 3/120 11 5/110 24 50 56 30 50 1由指定時間及在指定溫度下加熱浸漬纖維所製備之預漬醴 ......................................................^..............................-ίτ (請先聞讀背面之注意事項再填寫本頁) 線 經濟部中央揉準局印裝 甲 4(210Χ· 297:;:发) -23 olt^ 五、發明説明(22 ) A6 B6 參AB 5. Description of the invention (20) Example number 6 7 8 9 10 11 Epoxy resin 1 (g) 100 100 100 100 70 100 Cyclo-vaporide resin 2 (g) 30 Latent hardener 1 (g) 35.1 Latent Hardener 2 (g) 38 Latent hardener 3 (g) 32.9 27.4 6 2,4-pyridine- (Ν, Ν'-dimethylurea) -toluene (g) 6 1,4-bis- (Ν, Ν '-Dimethylurea) -benzene (g) 6 1-benzaldehyde-2-isopropylimidazole (g) 2.3 1- (2 ·, 4', 6, -trimethylphenyl) -2-benzene Gemazole (g) 3 1-ethyl-2-ethyl-4-methylimidazole (g) 1.7 isoflurane_diamine (g) 2.1 2.3 2 2.75 2 2.33 CapCure ® 3-800 5.4 Triethyl Glycol dithiol 5.8 7 4 7 Triol propyl propane trithioglycolate 7.3 b stage maximum (υ) 68 86 102 128 127 97 c stage maximum (υ) 133 143 151 162 171 159 (please read the notes on the back first Please fill in this page again.). Installed. • Ordered.. _ The Central Bureau of Economic Affairs of the Ministry of Economic Affairs printed the cracked armor 4 (210X 297 issued) 5. Description of the invention (21) A6 B6 Table 2: Pre-clearing body (PP): > The composition of Yung No. 1 point for PP preparation / it is up to X high days = medium ^ sleep viscosity is low and X days dad is very good & good catchability 1 10/100 11 15 16 11 15 2 10/100-30 45 48 58 5/110-30 45 45 50 3/120-30 45 40 45 3 5/110 17 24 30 20 30 4 5/110 14 19 22 14 22 5 5/110 10 20 22 14 22 6 5/110 7 10 14 7 12 7 5/90 3 6 7 3 7 8 5/100 1 7 18 7 18 9 5/110 5 20 26 20 26 4/120 5 12 18 12 18 10 5/100 — 10 16 10 16 3/120 11 5/110 24 50 56 30 50 1 Pre-stained mash prepared by heating and impregnating the fiber at the specified time and temperature ........................... ........................ ^ ......................... ...........- ίτ (please read the precautions on the back and then fill out this page) The Armored Printed Armor 4 (210Χ · 297:;: issued) by the Central Bureau of Economic Development of the Ministry of Line Economy -23 olt ^ V. Description of the invention (22) A6 B6

N 經濟部中央標準局印裝 甲 4(210X297么'爱) m 130CJ琺35Φ皤0NCT琛蓮砘器摧_疵想。 mlsoci酿 35ΦΚ淘<ΓΓ萍!f 樾 as:iM-T(Hettleer TA 3000)。 m130rf联 35冰》湔泠萍 If-樾座 S 卟 W 啓 22|_ _ 豳«δπΝ· a-ssl:«进葙! Α鉍菊泠萍3|蓮||-;8鈔菊存涔|0|筇溪兴 1、> «鵁闽蓥筇。 iflfaTechne Gelation TBer GT3MIt 〇 蓮wsf^Nl·娌盡韵a漤。 -^3 C» CJl CO ts5 1—* 實施例 编號之 組成物 3473 3424 3191 2947 3364 3212 撓曲試 彈性模數 (N/mn 2 ) 143 131 116 110 110 81 = 一 s砷二 t〇 C〇 私私知 ^ Ol CJ1 t^O 05 CO 3 452) 外纖維度變 ⑴ 115 114 114 104 119 110 108 Tg 2 (V ) CTl〇5〇3 0303-^3-^30¾ -^305-0 *^<DOtOO〇 — 〇5C〇 ococooro ILS (AST A (N/mm 2 ) 66.0 69.7 67.3 68.0 60.8 65.6 65.3 53.1 M-D-2344): B (N/mm 2 ) ►-a i tO t—* i—* CJItOCO »—»4^.Ca3C0C0 Ϊ :PP變化 丨(天數) i- 54 13,5 >72 70 80 1 21.9 9.3 在50Ό膠 凝時間4 (小時) 5000 5600 1040 1120 1000 8300(RT) 1600 在55T:之 黏度5 (mPa.s) 鎺3 :闺班麥atlMb许玛菡N-fi.g ......................................................¾..............................tr...................................終 (請先閲讀背面之注意事項再填寫本頁) 24 ,ον ‘ A6 B6 五、發明説明(23 ) 新鮮 5天 15天 II 12,46" 11,11 ” 11,53,, 1 醪凝時間 [分/秒] 新鮮 3天 15天 II 12'00” 14,40: 15 Ό6" 2 膠凝時間 [分/秒] 新鮮 5天 16天 II 10Ί5" 14'19" 13'44" 3 膠凝時間 [分/秒] 新鮮 4天 12天 II 10'20" 13,31” 12'41" 4 膠凝時間 [分/秒] 浙4:科1203铨连签:>羅睡»囤耷扯猱甜砑锄费雄涵N Printed Armor of the Central Bureau of Standards of the Ministry of Economic Affairs Armor 4 (210X297 M'Ai) m 130CJ enamel 35Φ 皤 0NCT Chen Liantan stoneware. mlsoci stuffed 35ΦΚ 淘 < ΓΓ 萍! f 樾 as: iM-T (Hettleer TA 3000). m130rf 联 35 冰 "Yeling Ping If-Yi Zuo S porch W Revelation 22 | _ _ 豳« δπΝ · a-ssl: «Jin Wei! Alpha bismuth chrysanthemum 3 | lotus ||-; 8 chrysanthemum chrysanthemum | 0 | Qunxi Xing 1, > iflfaTechne Gelation TBer GT3MIt ○ lotus wsf ^ Nl · Wu Jinyun a 漤. -^ 3 C »CJl CO ts5 1— * Composition of example number 3473 3424 3191 2947 3364 3212 Flexural test elastic modulus (N / mn 2) 143 131 116 110 110 81 = one s arsenic 〇Private knowledge ^ Ol CJ1 t ^ O 05 CO 3 452) External fiber degree change ⑴ 115 114 114 104 119 110 108 Tg 2 (V) CTl〇5〇3 0303- ^ 3- ^ 30¾-^ 305-0 * ^ < DOtOO〇- 〇5Cococooro ILS (AST A (N / mm 2) 66.0 69.7 67.3 68.0 60.8 65.6 65.3 53.1 MD-2344): B (N / mm 2) ►-ai tO t— * i— * CJItOCO »—» 4 ^ .Ca3C0C0 Ϊ: PP change 丨 (days) i- 54 13,5 > 72 70 80 1 21.9 9.3 at 50Ό gel time 4 (hours) 5000 5600 1040 1120 1000 8300 (RT) 1600 at 55T: Viscosity 5 (mPa.s) 鎺 3: Mai Ban Mai atlMb Xu Mahan N-fi.g ................................. ..................... ¾ ............................... ........ tr ............................. End (please read the back first Note, please fill out this page) 24, ον 'A6 B6 V. Description of the invention (23) Fresh 5 days 15 days II 12,46 " 11,11 ”11,53 ,, 1 Mash setting time [minutes / second] Fresh 3 days 15 II 12'00 ”14,40: 15 Ό6 " 2 gel time [min / sec] fresh 5 days 16 days II 10Ί5 " 14'19 " 13'44 " 3 gel time [min / sec] fresh 4 days 12 Day II 10'20 " 13,31 ”12’41 " 4 Gel time [minutes / second] Zhejiang 4: Ke 1203 Quan Lianlian: > Luo Sleeping» Hoarding and Cultivation Fei Xionghan

0 ^ 謝锒 m 17>H (請先聞讀背面之注意事項再填寫本頁) •装. •訂· .綠. 經濟部中央標準局印裂 甲 4(210X 297 公沒) 激® a 【冰/2 1105" 14-37- 1409" 25 A6 B6 五、發明説明(24 ) 表5:鋁Η條與預漬體黏合做為預漬體儲存在室溫之 功能時間之黏着劑的抗剪強度 抗剪強度 儲存期間 (DIH 53 283) [N / Hi m 2 ] [N / b m 2 ] 1天 15.1 14.2 5天 11.9 11.6 9天 13.9 14.9 15天 12.1 13.2 {請先閲讀背面之注意事項再填寫本頁) _襄· .訂· 管掄例12:濑宙樹脂流動作為餻存梧清钃之功能時間 預潰體之可用性一般僳測定其流動以做參考。如流動 量太少時,例如少於1 0 % ,則預漬體無法加壓而獲得良 好之層製品。 秤量( = W1)邊長為5公分之2平面預潰體(使用實施例 2製備),正確地叠合放置於2張分離紙間加壓預熱至 1001C。立即開閉沖壓機並加壓至2MPa.5分鐘後,自熱 —26 — 甲 4(210Χ 297 公尨) .線. 經濟部中央標準局印製0 ^ 谢 锒 m 17> H (please read the precautions on the back and fill in this page) • Installed. • Ordered.. Green. The Central Bureau of Standards of the Ministry of Economic Affairs printed the cracked armor 4 (210X 297 public) ji® a 【 Bing / 2 1105 " 14-37- 1409 " 25 A6 B6 V. Description of the invention (24) Table 5: Adhesion of aluminum H strip to the pre-preservation body as a function of the pre-preservation body stored at room temperature for the adhesive shear resistance Strength Shear strength storage period (DIH 53 283) [N / Hi m 2] [N / bm 2] 1 day 15.1 14.2 5 days 11.9 11.6 9 days 13.9 14.9 15 days 12.1 13.2 {Please read the notes on the back before filling in This page) _XIANG · .BOOK · GUAN Guan Example 12: The availability of Setju resin flow as a functional time-pre-destructor of Fu Cunwu Qingjing. The flow is generally measured for reference. If the flow volume is too small, for example less than 10%, the pre-stain cannot be pressurized and a good laminate is obtained. Weighing (= W1) 2 flat pre-collapsed body with side length of 5 cm (prepared using Example 2), correctly stacked and placed between 2 separate papers and preheated to 1001C under pressure. Immediately open and close the press machine and pressurize to 2MPa. After 5 minutes, self-heating — 26 — A 4 (210Χ 297 g). Line. Printed by the Central Bureau of Standards of the Ministry of Economic Affairs

五、發明説明(25) 壓機取出成形之層製品,沿層製品邊綵切掉流出之樹脂 。再秤置層製品的重量( = w2), wl和w2間之重量差以χ表 示可獲得"流動”之重量百分比。 預潰體在室溫 樹脂之流動 之儲放期間 U重量) 1天 19.3 4天 21.0 11天 20.8 奮旃例HI :使用甜成物做為執熔反座件黏着劑 經由儲存安定性形成B階段後測定表6中所掲載之組 成物。熱熔融物之黏度(以Contraves AG, Zurich製造 之Rheonat Viscometer加以計測)經由各種儲存時間,其 熱度和機械強度俗如表7所示,結合鋁Η條之黏着劑 (在160*0硬化30分鐘)之抗剪強度偽如表8所示。 促進劑 1: Chorotoluron 促進劑2:下式之眯唑啉5. Description of the invention (25) The press takes out the formed layered product, and cuts out the resin flowing out along the edge of the layered product. Re-scale the weight of the layered product (= w2), the weight difference between wl and w2 is expressed in χ as a percentage of " flowable " weight. The weight of the pre-crushed body during storage at room temperature of the resin U weight) 1 day 19.3 4 days 21.0 11 days 20.8 Endeavour Example HI: Use sweet as the adhesive for the melting anti-seating component to form the B stage after storage stability to determine the composition contained in Table 6. The viscosity of the hot melt (in (Measured by Rheonat Viscometer manufactured by Contraves AG, Zurich) After various storage times, the heat and mechanical strength are shown in Table 7, and the shear strength of the adhesive (hardened at 160 * 0 for 30 minutes) combined with aluminum H is as false It is shown in Table 8. Accelerator 1: Chorotoluron Accelerator 2: Mizoline of the following formula

甲4(210X 297公发) (請先閲讀背面之注意事項再填寫本頁) .裝. .訂. •線· 〇V‘ -- 3 A6 B6 五、發明説明(26 ) (衍自EP-A 288359之實施例1) 促進劑3: 2,4,6-三-(二甲胺基甲基)-酚和酚/酚β清 漆樹脂 M Grade s-2(Maruzen Petrschenica KK, Tokyo)之固體溶液,依 EP-A 200,678 加以製備(促進劑VI ) 促進劑4:聚乙烯酚樹脂M Grade s-2(Maruzen Petrochenical KK, Tokyo),對甲醛和二 甲胺之曼尼期(Mannich)反應生成物,依照 EP-A 351,365之方法加以製備(促進剤XI) 表6:熱熔融物之組成物 (請先閲讀背面之注意事項再填寫本頁) • f 經 濟 部 中 央 標 準 局 印 裂 實施例 13 14 15 16 環氣化物樹脂1 (克) 10 10 10 10 二氰二醛胺(克) 1 0.3 0.96 0.96 促進劑1 (克) 0.05 促進劑2 (克) 1 促進劑3 (克) 0.04 促進劑4 (克) 0.04 異佛爾酮二胺(克) 0.11 0.11 0.11 0.11 三乙二醇二硫酵(克) 0.25 0.49 0.49 0.49 -28 .訂. *線. 甲 4(210X 297y 簷) 五、發明説明(27)A4 (210X 297 public issue) (please read the precautions on the back before filling in this page). Packing. Ordering. • Line · 〇V '-3 A6 B6 5. Description of the invention (26) (derived from EP- Example 1 of A 288359) Accelerator 3: 2,4,6-tris- (dimethylaminomethyl) -phenol and phenol / phenol β varnish resin M Grade s-2 (Maruzen Petrschenica KK, Tokyo) solid The solution was prepared according to EP-A 200,678 (accelerator VI). Accelerator 4: Polyvinylphenol resin M Grade s-2 (Maruzen Petrochenical KK, Tokyo), produced by the Mannich reaction of formaldehyde and dimethylamine It is prepared according to the method of EP-A 351,365 (promoting XI) Table 6: Composition of hot melt (please read the notes on the back before filling in this page) 14 15 16 cyclic gasification resin 1 (g) 10 10 10 10 dicyandialdehyde (g) 1 0.3 0.96 0.96 accelerator 1 (g) 0.05 accelerator 2 (g) 1 accelerator 3 (g) 0.04 accelerator 4 (g) 0.04 Isophorone diamine (g) 0.11 0.11 0.11 0.11 Triethylene glycol disulfatase (g) 0.25 0.49 0.49 0.49 -28. Order. * Line. A 4 (210X 297y eaves) 5. Description of the invention (27)

表7:熱熔融物之性質 實施例 13 14 15 16 在40C儲放後之黏度(Pas) 1天 9.3 15.5 15.3 12天 13.2 14天 19.1 15.7 28天 22.6 19.5 B階段最大(¾ ) 111.4 144.5 111.0 111.5 C階段最大ΓΌ ) 159.9 160.5 171.5 182.5 在140Ό膠凝時間 10'43" 13.26" 13'50" 27,02" C階段後之玻璃轉移溫度Tg 116¾ 136¾ 116^ 103*C 表8:硬化後(30分/1600黏着劑之抗剪強度(DIN 53 283) 實施例 13 14 15 16 儲存 40天 /RT 1 天 /40TC 1 天 /40Ό 1 天 MOC 抗剪強度(Ν/πμβ 2 ) 21.1 20.9 25.8 25.7 (請先閲讀背面之注意事項再填寫本頁) .裝· .訂. 奮旃例17:紺成物做為黏羞鎊曄使用 樹脂組份: 將75克之環氣化物樹脂1加熱攢拌至80-100Ό,然後 份添加以25克之細研磨環氣化物樹脂2 。在80-100Ό繼 缠攪拌直至完全溶解為止。 -29- 甲4(210X 297公发) •線. 經濟部中央標準局印製 ^ A6 B6 五、發明説明(28 ) 硬化劑組份: 將23,3克之(^丨〇「〇1;〇114「〇11,15.2克之三乙二醇二硫 酵和13.9克之異彿爾酮二胺充分混合。添加47.6克之二 氰乙二酵胺於所生成之懸浮液並將混合物分散於溶解器 得白色之膠漿。100扮重之樹脂組份混合以15份重之硬 化劑同時用於不鏃布(由荷蘭Lantor公司産製之Firdt 3255 EL>。於形成為B階段後(在U0C5分鐘)得樹脂含 量約80%之黏着劑薄膜。 黏着劑結合於鋁片條(在129C硬化30分鐘)之抗剪強 度(D I Ν 5 3 2 8 2 )為 2 0 N / m β 2。 (請先閏讀背面之注意事項再填寫本頁) .蛑. .訂· •線. 經濟部中央標準局印装 甲 4(21〇Χ 297公发)Table 7: Properties of hot melt Example 13 14 15 16 Viscosity after storage at 40C (Pas) 1 day 9.3 15.5 15.3 12 days 13.2 14 days 19.1 15.7 28 days 22.6 19.5 Phase B maximum (¾) 111.4 144.5 111.0 111.5 (Maximum ΓΌ in C stage) 159.9 160.5 171.5 182.5 Gel time at 140Ό 10'43 " 13.26 " 13'50 " 27,02 " Glass transition temperature Tg after stage C 116¾ 136¾ 116 ^ 103 * C Table 8: After hardening ( Shear strength of 30 minutes / 1600 adhesive (DIN 53 283) Example 13 14 15 16 Storage 40 days / RT 1 day / 40TC 1 day / 40Ό 1 day MOC Shear strength (Ν / πμβ 2) 21.1 20.9 25.8 25.7 (Please read the precautions on the back before filling in this page). Packing. Ordering. Endeavor Example 17: The cyan product is used as a sticky pound. Use the resin component: Heat 75g of the ring gasified resin 1 and stir until 80-100Ό, and then add 25 g of finely ground ring vaporized resin 2. Continue winding and stirring at 80-100Ό until it is completely dissolved. -29- A4 (210X 297 public) • Line. Printed by Central Bureau of Standards, Ministry of Economic Affairs Preparation ^ A6 B6 V. Description of the invention (28) Hardener component: 23,3 grams ^ 丨 〇``〇1; 〇114 '' 〇11, 15.2 grams of triethylene glycol disulfatase and 13.9 grams of isophorone diamine are thoroughly mixed. Add 47.6 grams of dicyandiethylene glycol to the resulting suspension and Disperse the mixture in a dissolver to obtain a white glue. Mix 100 parts of resin component with 15 parts of hardener at the same time and use it for non-twisting cloth (Firdt 3255 EL> manufactured by Lantor of the Netherlands. Formed as B After the stage (5 minutes at U0C), an adhesive film with a resin content of about 80% is obtained. The shear strength (DI Ν 5 3 2 8 2) of the adhesive bonded to the aluminum strip (hardened at 129C for 30 minutes) is 2 0 N / m β 2. (Please read the precautions on the back before filling in this page). Insects.. Orders • Lines. Armored 4 printed by the Central Standards Bureau of the Ministry of Economic Affairs (21〇Χ 297 public)

Claims (1)

IL 、呻:〇v‘ •f. 各 W 年 ,: _ ............$ ;t.;h D7 經濟部中央標準局R工消费合作社印製 六、申請專利範圍 第79 1 09 6 86號「含潛硬化胺及硫酵之可硬化環氣樹脂 混合物」專利案 (81年12月修正) 1. 一種可硬化混合物,包含 (a) 環氣樹脂,為雙酚A二縮水甘油醚或琛氣甲酚酚酚醛 清漆, (b) 佔成份(a) 3〜40重鼉%的二氰二醯胺或4-4’-二胺 基二苯基颯, (c>佔成份(a) 1〜10重量%的胺,偽選自含正—辛基胺 ,異氣爾酮二胺,1,8 -二胺基—3,6 -二噁辛烷,4,4, -二胺基環己基甲烷和1,2 -二胺基琿己it完及 (d)佔成份(a) 1〜10重量%選自含三甘醇二硫酵和三甲 醇丙烷三硫代乙二醇酯之基圃和含式 R+〇~^CH:CHO^^H:CpCH:SH]3 Cri3 〇H 其中η = 1- 2及R為一脂族烴的三镟基。 2. 如申請專利範圍第1項之混合物,其中環氣樹脂(a)為 液髓。 3. 如申請專利範圍第1項之混合物,其中除組成份(a)至 (b )外亦包含有琛氣樹脂(a )與潛硬化劑(b )反應中之 促進劑U),其為眯唑或脲衍生物。 1 本紙張尺度速用中B國家標準(CNS)甲4规格(210 X 297公*) (請先閲讀背面之注意事項再塡寫本頁) -裝- .11. 線·IL 、 呻: 〇v '• f. In each W year: _ ............ $; t.; H D7 Printed by R Industrial and Consumer Cooperative of Central Bureau of Standards, Ministry of Economic Affairs Scope No. 79 1 09 6 86 Patent Case for "Hardenable Amine Resin Mixture Containing Latent Hardening Amine and Sulfur Fermentation" (Amended in December 81) 1. A hardenable mixture containing (a) a ring gas resin, which is a double Phenol A diglycidyl ether or cresol cresol novolac, (b) dicyandiamide or 4-4'-diaminodiphenylsac, which accounts for 3% to 40% by weight of component (a), (( c> 1 to 10% by weight of the amine of component (a), pseudo-selected from n-octylamine, isophorone diamine, 1,8-diamino-3,6-dioxoctane, 4 , 4, -Diaminocyclohexylmethane and 1,2-diaminohexyl and (d) account for component (a) 1 ~ 10% by weight selected from triethylene glycol-containing dithiol and trimethanol propane trioxide The thioglycol ester base and the formula R + 〇 ~ ^ CH: CHO ^^ H: CpCH: SH] 3 Cri3 〇H where η = 1-2 and R is an aliphatic hydrocarbon triglyceryl group. 2 . If the mixture of the first item of the patent application scope, the ring gas resin (a) is the liquid pith. 3. If the mixture of the first item of the patent application scope. In addition to the components (a) to (b), it also contains the accelerator U) in the reaction of the gas resin (a) and the latent hardener (b), which is a azole or urea derivative. 1 This paper size is used in the B National Standard (CNS) A4 specification (210 X 297 g *) (please read the precautions on the back before writing this page) -installed- .11. Thread · A7 B7 C7 D7 六、申請專利範園 4如申請專利範圍第1項之混合物,傜用以漫漬所得的繼 維複合材料。 5. 如申專利範圍第1項之混合物,偽經由硬化生産交聪 生成物。 6. 如申諳專利範圍第4項之混合物,其中所使用的繼維複 合材料傜藉完全硬化以生産製品。 經濟部中央揉準局員工消费合作社印製A7 B7 C7 D7 VI. Application for patent Fan Garden 4 For example, the mixture of item 1 of the patent application scope is used to diffuse the obtained composite materials. 5. If the mixture of item 1 of the patent scope is applied, the product will be produced through hardening. 6. For example, if you apply for the compound in item 4 of the patent scope, the secondary-dimensional composite material used in it is completely hardened to produce products. Printed by the Employee Consumer Cooperative of the Central Ministry of Economic Affairs
TW79109686A 1989-11-21 1990-11-16 TW201779B (en)

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