TW297180B - - Google Patents
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- TW297180B TW297180B TW084113516A TW84113516A TW297180B TW 297180 B TW297180 B TW 297180B TW 084113516 A TW084113516 A TW 084113516A TW 84113516 A TW84113516 A TW 84113516A TW 297180 B TW297180 B TW 297180B
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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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
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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
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
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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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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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
- C10M117/00—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
- C10M117/02—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
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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
- C10M117/00—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
- C10M117/08—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to a carbon atom of a six-membered aromatic ring
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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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/20—Thiols; Sulfides; Polysulfides
- C10M135/28—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring
- C10M135/30—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups; Derivatives thereof
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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
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/04—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing propene
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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
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/06—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing butene
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/08—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing aliphatic monomer having more than 4 carbon atoms
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/10—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing aromatic monomer, e.g. styrene
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- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/12—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing conjugated diene
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/44—Mechanical structures for providing tensile strength and external protection for fibres, e.g. optical transmission cables
- G02B6/4401—Optical cables
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/46—Bases; Cases
- H01R13/52—Dustproof, splashproof, drip-proof, waterproof, or flameproof cases
- H01R13/5216—Dustproof, splashproof, drip-proof, waterproof, or flameproof cases characterised by the sealing material, e.g. gels or resins
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- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02G—INSTALLATION OF ELECTRIC CABLES OR LINES, OR OF COMBINED OPTICAL AND ELECTRIC CABLES OR LINES
- H02G15/00—Cable fittings
- H02G15/003—Filling materials, e.g. solid or fluid insulation
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- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02G—INSTALLATION OF ELECTRIC CABLES OR LINES, OR OF COMBINED OPTICAL AND ELECTRIC CABLES OR LINES
- H02G15/00—Cable fittings
- H02G15/08—Cable junctions
- H02G15/10—Cable junctions protected by boxes, e.g. by distribution, connection or junction boxes
- H02G15/117—Cable junctions protected by boxes, e.g. by distribution, connection or junction boxes for multiconductor cables
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
- C10M2201/103—Clays; Mica; Zeolites
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/105—Silica
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/104—Aromatic fractions
- C10M2203/1045—Aromatic fractions used as base material
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- C10M2203/106—Naphthenic fractions
- C10M2203/1065—Naphthenic fractions used as base material
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- C10M2203/108—Residual fractions, e.g. bright stocks
- C10M2203/1085—Residual fractions, e.g. bright stocks used as base material
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- C10M2205/024—Propene
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- C10M2205/026—Butene
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- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
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- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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- C10M2207/1225—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic used as thickening agent
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- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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- Compositions Of Macromolecular Compounds (AREA)
Description
A7 B7 經濟部中央標準局負工消費合作杜印« 五、發明説明( 明領域 本發明一般係充填膠凝油組合物之電信裝置。本發明尤 係電信裝置,尤爲内有電連接點、轉接點或分接點之接線 盒,以膠凝油組合物保護以免潮濕腐蝕, 议住為含鋁複基 皂之組合物。 背景 電信裝置,如電纜線、貞載線、内有分接點、轉接點或 其他接點之接線盒及其他電氣裝置常暴露於破壞環境條件 下。然而在其至少4〇年服務期間卻需保持其機械、電氣及 環境特性。在過去,電輯線吊於地面上電線桿間,偶而 置於水下。逐漸地,爲了美觀及保護免於高溫、大雨、大 雪、結冰、強風及落樹等理由,這些電纜線埋於地下。然 而,即使埋於地下,這些裝置於重塡平時受到機械撞擊”,、、 受濕氣侵蝕,可能沉陷及暴露於鹽份及其他腐蝕物中。 内有分接點、轉接點或其他接點以連接電纜線與電纜線 或連接電境線與電信裝置之接線盒,雖然常置於罩殼中1 若不能密封好,常易受如潮濕腐蝕物之環境破壞。一般言 之,矽油潤滑劑、彈性封膠或黏膠封條已試圖用於阻絕^月 濕。雖然這些密封劑提供一些保護,尤其接線盒埋於地下 時,潮濕常能滲入罩殼中造成短路中斷通訊服務。 電信服務纜線通常受到良好保護。服務境線常含_大束 絕緣銅線、覆蓋該束線之保護金屬罩及塑膠或其他絕緣物 外鞘。此架構通常足以保護纜線。然而,若服務纜線保護 外鞘已切斷或破掉,水可滲至線上延線漫延。此尤當浸入 本紙張尺度適用中國國家標準(CNS ) Μ規格( (請先閲讀背面之注意事項再填寫本頁) 裝. 、νβ 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 ·) 線已切斷時尤眞。爲保護免於此狀況,纜線以抗濕充填组 合物塡充。 在分接點、轉接點或其他接點,服務纜線之金屬罩及保 護外稍需移除以連接兩或更多服務纜線或裝置内之電線。 這些連接需要將長服務纜線接絡,連接至服務區及使服務 連至個別用户處。在未保護區,接點腐蝕或濕氣或其他異 物造成短路會永遠干擾設施。更換或修理埋覆電信裝置或 任何服務干擾將很困難昴貴。因此,罩殼内填充保護性抗 濕充填組合物以保護電信裝置以免潮濕腐蝕。 多種電is裝置,其需保護免潮濕,如述於明尼蘇逵州礦 業製—造公立刊行名爲"電氣產品"説明小册内。在提供電信 裝置保護時,需小心保持其機械、電氣及環境特性不被破 壞。因此,電信裝置之保護性抗濕充填組合物之配方不但 需提以免潮濕腐蚀,同時亦需不破壞電信裝置之機械、電 氣及環境特性。再者,保護性充填組合物不能化學性破壞 服務纜線成份或轉接I故。 電仏裝置對保護性充填組合物之需要不易滿足。保護性 充填組命物在服務纜線及接線盒使用溫度範圍内(至少由_ 4(TC至70X:)需保持穩定。若保.護性充填組合物之最高工作 溫度沒有至少跟電氣成份者一樣高,則充填組合物將會到 達降低其黏度流出罩殼之溫度,使裝置潮濕腐蚀。再者, 充填組合物在Μ安裝溫度時必需可流動以完全充 填而無弄破或過度擠壓電氣成份。 保護性充填組合物亦應夠黏以保持罩殼緊壓而不會在組 本錄尺度適财ϋϋ家標準(CNS-)~Α;^7ϋ97公釐) -------------^------IT------ - < { (請先閱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、:4印製 297180 五、發明説明(3 .) '" 合物表面及裏面形成空隙。同時,保護性充填組合物亦應 夠軟黏需不會過度緊壓至電氣成份,但是若服務境線終端 暴露於淹水人孔中,仴需抗重力及水壓而不會流出。 技藝中習知膠凝劑如黏土及疏水性煙化氧化矽,可用作 膠凝油配方中有效保護充填組合物。然而因爲有效凝膠需 要*大量疏水性煙化氧化矽故爲筇貴。再者使用疏水性煙 化氧化矽會造成製成凝膠易磨蝕。 因此需要具較優抗潮濕腐蝕特性之電纜線脂類保護性充 填組合物,而無氧化碎基配方之研磨性。 發明概诚 本發明一般係以膠凝油组合物保護電信裝置及服務纜線 以免潮濕腐蝕。本發明尤係以充填膠凝油組合物罩殼保護 電#接線盒及其類。膠凝油含亦含烴基油、防滲劑、鋁複 皂及任意量抗氧化劑及降傾點劑。膠凝油尤適於充填服務 境線及接線盒之罩殼内轉接點、分接點或其他聯接點及裝 置之四周。 依本發明提供尤適於充填電信裝置之膠凝油組合物。膠 凝油組舍物包含如煙基油類之油成份、一或多種防渗劑及 銘複。膠凝油可包含随意量之抗氧化劑及降傾點劑。油 成份可爲至少任一礦物油’較優爲食物級礦油、環燒油' 石蠛基油或聚-or 肺烴。 膠凝油組合物含40-90%(較優50-75%)之油成份、5-50%(較 優25_45%)之防滲劑、及4-15%(較優6_12%)之脂肪酸及芳香 酸之鋁複皂。製備鋁複皂之脂肪酸含至少一硬脂酸、油 本紙張尺度賴t關家榇CNS ) Λ4規格(210X297公廣) (請先閱讀背面之注意事項再填寫本頁) 装. 訂 A7 A7 經濟部中央標準局員工消費合作社印裝 ________ 五、發明説明(4 ) 酸、十四酸 '癸酸、及棕櫚酸。防滲劑可含嵌連共聚物, 如橡膠化合物及己聚合化油具芳香成份小於6。/0之少於1〇個 咬原子之烴類。有效橡膠成份包含丁基橡膠、乙烯基-丙烯 基、乙烯基-丙烯基-二體橡膠、氯化橡膠及熱塑性橡膠嵌 段共聚物。嵌段共聚物及聚合化油混合物爲較佳防滲劑。 抗氧化劑之隨意量可爲〇. 1至2%重量。/〇。抗氧化劑包含被立 體阻隔化之驗類化合物,其含硫鏈。 本發明膠凝油組合物具較佳保護性且比氧化矽基產品較 不易磨蚀。再者,這些膠凝油組合物可用於電信及其他電 氣裝置内做爲保護性充填組合物,同樣可達到與氧化矽基 配方相同黏度但只需甚少量之膠凝劑。 特適用作電信裝置免潮濕腐蚀之保護性充填組合物的膠 凝組合物包含20-90%如礦物油及5_5〇%防滲劑,其中痛物油 比防滲劑之重量%爲7: 3至!:丄,在鋁複良中之脂肪酸比芳 族酸莫耳比爲約1 : i,鋁複皂中鋁比(脂肪酸加芳族酸)之莫 耳比爲約1 : 2。 經概述本發明,本發明以下説明書及非限制性實例詳述 本發明 '除非另予指明,所謂百分比以重量爲準,所有溫 度爲攝氏。 圖面簡述 本發明較優實施例可參照所附圖面而更了解,其中: 圖1爲直路接合連接器之遠視圖;及 圖2爲圖1連接器底部視圖以分析其中線路連結。 發明詳述 -7 - 本紙張尺度適用中國--——-_ I-------'-I裝------訂-----7 旅 . f ♦ (請先閲讀背面之注意事項再填寫本頁) A7
五、發明説明( 經濟部中央標準局員工消費合作社印製 本發明膠凝油組合物一般係含油成份、鋁複良、防參 劑、及任意量抗氧化劑及降傾點劑。本發明較優實例:以 膠凝油組合物充填於電信裝置内及四週以保護這些 免潮濕腐蝕。 在較優實例中,電信服務纜線之金屬罩覆蓋—大亊銅電 線在電纜中,其中填充有本發明膠凝油組合物以保護電^ 及' 連接電線之裝置在境線切斷時免於潮濕。 參見圖1及2,其説明本發明較優實施例,其中直路接入 連接於兩片罩殼1〇中,以保護以免潮濕腐蝕。罩殼包括了^ 祁11及底邵12,其加上側面重疊組成,於内留下一微平區 域13以進行連接。罩殼通常由於底部14之接線盤14 '在頂 部、底部或側面之服務纜線16、17之入口 15所組成。由月良 務纜線中心移除絕緣物18,且個別服務線19連接至栓上 以如插銷或夹子之鎖住裝置21固定於接線盤14上以連接輸 入纜線16至輸出纜線17。頂部以本發明膠凝油組合物填 充。爲組裝罩殼以保護其内之電氣連結,罩殼之蓋子首先 ,.對齊底邵之接線盤。罩殼而後以手壓擠緊密直至任何空氣 及罩设取務欖線口充滿膠凝油充填組合物。結果,膠凝油 形成濕氣阻隔完全去除水份而保護電氣連結以免潮濕腐 蚀;接線盒在封閉後可立刻埋入土中。 罩殼可以任何熟諳此技藝者所習知之抗腐蚀材料製成, 該材料能忍受暴露於潮濕及腐蝕物質、且忍受裝置埋入土 中時之物理應力及衝擊。相似地,地下應用軍殼結構物質 必須能承受當裝於電線样上時之高溫、強風、大雨、結 本紙張尺度適用中國國家標準(CNj; ) a4規格(210X 297公釐) —i— 裝 訂 I---1旅 (請先閱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裝 A7 B7 五、發明説明(6 ) 冰、大雪、及日曬。 電氣成份之導電金屬線一般含銅。習知技藝中所熟知者 爲多種等級及型式銅及銅合金習知可應用於此。 膠凝油組合物重量含約40-90%(較優50-75%)之油成份、約 5- 50%(較優25-45%)之防滲劑、及約4-15%(較優5-12%,更優 6- 10%)之鋁複皂。降傾點劑之隨意量可爲組合物重量之約 0.5至10%(較優1-3%)且抗氧化劑之隨意量可爲組合物重量之 約 0.1 至 2%(較優 〇.5至 1.5%)。 - 本發明膠凝油之製成一般爲在油成份存在時就地形成鋁 複皂。油成份包含一或多防滲劑及任意量之抗氧化劑和降 傾點劑。 膠凝油組合物之油成份可爲如礦物油、具10個碳或更少 且已聚合成油之α -烯烴、環烷油或石蠟基油。較優油成份 爲,更優爲食品級礦物油。特殊有用之烴類油具苯胺點高 於220°F、閃點至少350°F、較優500°F、黏度在100°F爲65-600沙巴特宇宙秒(SUS),較優爲530SUS,且具平均數目分子 量至少300,較優大於400。 爲本堯明目的計,下列諸項意義如下: ⑻所謂"石蠟基油"意謂具重黏度常數介於0.78至0.85(皆含) 之礦物油,該常數以依美國材料試驗協會D-25〇l-67步據測 定,其具最少65%石蠟基碳原子及最多5重量%之芳族碳原 子。 (b)所謂"環烷油"意謂具重黏度常數介於0.78至0.85(皆含) 之礦物油,該常數以依美國材料試驗協會D-25〇i_67 0 .驟測 -9 - 本紙張尺度k用中國^標準(CNS ) A4規格(210X297公'一'~~ I ; ^裝 訂 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央橾準局員工消費合作社印製 A7 B7 五、發明説明(7) 定,其具最少35%環烷基碳原子及最多5%之芳族碳原子。 用於本發明膠凝油之礦物油一般包括但不限於變壓器 油、錠子油 '電纜絕緣油及機油。有用環烷油包括但不限 於:賓利可(Pennreco)公司出品之得利卡(Drakeol)35,埃克森 (EXXON)公司出品之海灣白油(Coastal Pale Oils)及如得露沙 (Telura)309之得露沙油。有用石蟻基油包括但不限於埃克森 (EXXON)公司出品之白(Pale) 100及如得露沙(Telura)609之色 露沙油〇 - 依本發明,鋁複皂用作有效膠凝劑可對多種油立即調 整。鋁複皂組合物典型之變化以油成份苯胺點之不同而控 制脂防脂酸及芳族酸成份。鋁複皂配方之改變包括:芳族 酸對脂肪酸之莫耳比率、脂肪酸之碳鏈長度及總酸(脂防酸 加上芳族酸)對鋁之莫耳比率。脂肪酸:芳族酸之莫耳比率 一般由約1.4 : 0.6至0.6 : 1_4,且較優爲1 : 1。總酸:銘之比 率由1.8 : 1至2.2 : 1,較優爲1.9 : 1至2.1 : 1,最優爲2 :工。 技藝中習知,鋁複包之形成爲將有機鋁氧化合物與脂肪 酸及芳族酸反應而得。包之形成可在油成份存在時就形 成’或在形成後加入油成份中。較優地,皂之形成可在由 成份存在時就形成’其在高苯胺點礦物油(尤爲如賓利 一 (Pennreco)公司出品之得利卡(Drakeo〇500之碥物油)存右 1莫耳硬脂酸、1莫耳苯甲酸及三烷氧化三鋁反應而得。 多種脂肪酸可用以形成本發明所用之鋁複包。—般+ ,這些酸來自動物、蔬菜或海產。可用以提供内形成有用紹 複包之脂肪酸包括但不限於:具碳鏠長(^至C22之脂肪酸, -10 - 本紙張又度適用中國國家標準(CNS ) Α4現格(210Χ 297公瘦) | -裝 訂 Γ (請先閲讀背面之注意事項再填寫本頁) 經濟部中央樣準局員工消费合作社印製 五、發明説明(8 七優爲至C:22之脂肪酸,更優爲至ci8。有用脂肪酸例 仁不限於··硬脂酸、十四酸、癸酸、油酸、及棕櫚酸及其 I δ物。亦可用橡膠級硬脂酸及末氫化簡單牛脂脂肪酸。 可用以形成有用鋁複皂之脂肪酸未飽和量亦可不同。未 飽和的量以碘價衡量典型爲〇 5但可多至1〇至12。 可用以提供產生鋁複皂之鋁成份典型以烷氧化物型提 仏’較優爲異丙烷氧化物或其三體。其他有用鋁成份來源 之提供可以如辛醯氧銨之氧銨醯化物,及烷氧化銨鉗合物 如lA^hattem)化學公出卡塔林(Ketalin) 〇 可用做本發明膠凝劑之鋁複包可摻合以鹼金族或鹼土金 族金屬(如鈉 '鈣、鋰、鋇、鳃、鋅、鉛、鎘、鉀及其類金 屬)包。鋁複皀可再混合有額外增稠劑及膠凝劑。有用之額 外増稠劑及膠凝劑包括膨土、s夕石及g大花青,如具2至2〇個 脲鍵及分子量100至5,000之聚脲,如N-十二醯-L-氨基成二酸 -λ,/5 -二正丁醯胺之胺酸型油膠凝劑;如纖維素四銨鹽之 纖維素竹生物及糊精之脂肪酸g旨和其類。 可用做膠凝劑之鋁複皂的重量百分比可爲很廣。然而, 若鋁複皂之量增加,則形成膠凝劑配方之黏度及降服點亦 增加。 用於膠凝油組合物之防滲劑可爲合成烴類油或嵌連共聚 物及其混合物,較優爲混合物。低分子量合成油特適供防 滲劑。有用之合成油包括但不限於:α -烯烴類寡聚物,聚 合化C2-C9之烯,如聚丁烯、聚異戊烯、聚己烯、聚庚稀、 聚辛烯及聚壬晞和其類。最佳合成油防滲劑爲聚丁烯。 &張尺变適用中國國家揉準(CNS ) A4規格(210 x 297公釐) (请先閱讀背面之注意事項再填寫本頁) 裝-
,1T 297180 Α7
經濟部中央標隼局男工消費今作让印製 可用作防滲劑之聚合物例 ^ 乙締-丙烯橡膠、苯乙烯 丁二烯橡膠共聚物、苯 ^ 卿· 〇締-乙晞/丙烯橡膠共聚物、
烯-乙烯/丁烯-苯乙缔嵌連共 G 山、 共聚物、苯乙烯-異戊烯-苯乙嫌 敗連共聚物、及較優之苯乙嫌 乙烯/丙缔嵌連共聚物。 段共聚物於纽合物内重量較優爲〇 5至⑽。 乂 在較優可用作本發明防、 防/參劑i肷連共聚物爲苯乙烯-橡膠 嵌連共聚物。嵌連共聚物例有 W 4琛性敗連共聚物,如具苯乙 稀' -橡膠及苯乙婦-橡滕L _ ¥ 7* y + 琛膠苯乙烯者,具式爲(苯乙烯-橡膠)η之 敗連共聚物基,其中|^典开丨金^ T興型為3至4。在這些共聚物之有用橡 膠成份包括但不限於:異戊缔、丁二缔、乙晞/丙晞及其混 合物。這些共聚物典型具苯乙晞:橡膠比率爲介於約1: 9 至1 : 1間。特優嵌連共聚物爲苯乙締·乙缔/丙婦嵌連共聚 物,具苯乙 '烯:橡膠比率約〇 37 : 〇 63,未塑化、比重約 〇_93、裂斷強度(依美國材料試驗協會^^^〕方法)3㈨磅砰方 英吋’星化學公司出品商標名爲克勞頓(Kraton) 〇 1701 〇 可用於本發明膠凝油之隨减點劑包括海德克(Hitek) 672, 公司出品。條崤點劑爲膠凝油重量之約〇二至 2 /〇。可用於膠凝油之抗氧化劑包括被立體阻隔化之酚類化 合物’其含硫鏈。抗氧化劑之量可爲膠凝油〇丨至2%重量 /ο這些成份之特定百分比依膠凝油所欲應用之不同而有 變化。 特適用作保護性充填组合物之膠凝油配方中,鋁複皂之 形成爲在油成份存在下就地將鋁化物(如氧銨醯化物、烷氧 __ - 12 - 本紙張从相“目家@ ( CNS ) A4規格(21〇χ297公釐) ί : f^— (請先閲讀背面之注意事項再填寫本耳) -訂 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(w) 化銨鉗合物及鋁烷氧化物或其三體)中之1莫耳鋁與1莫耳硬 脂酸、1莫耳苯曱酸反應而得。苯胺點高之油,較優爲食品 級礦物油用以提供膠凝油充填組合物。具芳族成份0-11%, 環烷類成份3卜46%及石蠛類成份51-65%可用作接線盒充填 組合物。亦可包含防滲劑及任意量降傾點劑及抗氧化劑。 合適用供製造接線盒充填組合物之油包括但不限於:益 模(Puremore)# WOT 14,波利(Poly)-XH51 及波利(Poly)-M5IP, 皆由普馬卡(Burmah-Castrol)公司出品及殼牌(Shell)英國公司 出品之易得斯(Edelex)27。用以提供接線盒充填化合物之鋁 複皀約爲膠凝油组合物之4-30%。鋁複皂具鋁:總酸之莫耳 比率由1.2 : 1至1 : 1.9,且脂肪酸:芳族酸之比率由1.3 : 0.7至0.7 : 1.3,較優爲0.9 : 1.1至1.1 : 0.9。防滲劑可爲一或 多合成彈塑體,如苯乙晞-丁二晞嵌連共聚物及如聚丁烯之 合成油。較優可用作膠凝油填充化合物之油成份.在25 C具 黏度至少150厘泊。較優礦物油及聚丁烯之施用重量比率爲 6 : 4 0 特適用於電信裝置之膠凝油组合物配方爲含約54至56%礦 物油(食品級)之油成份,如賓利可(Pennreco)公司出品之登_ 利卡(DrakeoH 500、6-7%鋁複皂,34至36%之聚丁烯防滲 劑,如索特斯(Soltex)公司出品之索特斯(Soltex)PB32或阿馬 可(AMOCO)公司出品之阿馬可(AMOCO)H-300及1 %之抗氧化 劑,如汽巴嘉基(Ciba-Geigy)公司出品之索伊語(Irganox) 1035,及1至2%之防滲劑如殼牌(Shell)化學公司出品商標名 爲克勞頓(Kjaton) G 1701,反0.2%之降傾點劑。適用於接線盒 -13 - 本紙張尺度適用中國國家榡华(CNS ) 規格(210X297公釐) ! 裝 訂 ^ 今 A (請先閱讀背面之注意事項再填寫本頁) A7 A7 經濟部中央標準局員工消费合作社印製 B7 五、發明説明(11) 充填膠凝油配方之鋁複包中脂肪酸比芳族酸比率爲1:1,且 總酸(脂肪酸加芳族酸):鋁之比率爲2: 1。有用芳族酸包 括苯甲酸、對-甲苯甲酸、鄰-甲苯甲酸、二氣苯甲酸、π-莕甲酸、卢-莕甲酸、9-菲甲酸、3-菲甲酸、蒽醌α -羧酸、 蒽醌/3 -羧酸及去氫松香酸。 例1 在設有加熱套、攪拌器、滴管、氮入口及通氣管之樹脂 澆瓶中加入259.95克之得利卡(0^1^〇1)500、173.3克之聚丁烯 32及10克之克勞頓(Kraton) G 1701。氮氣可進入燒瓶中且加 入22.74克硬脂酸(酸値爲205.60)。攪拌形成混合物同時加熱 至100°C之溫度。點滴加入9克三異丙氧化三鋁(12.5%鋁)。加 入10克苯甲酸,溫度增至124°C,再點滴加入9克三異丙氧化 三鋁。再在49分鐘内溫度增至190°C。氮氣氛下攪拌並保持 溫度8分鐘。在17分鐘内混合物溫度冷至130°C。加入5克如 汽巴嘉基(Ciba-Geigy)公司出品之索伊諾(Irganox) 1035抗氧 化劑,及1克之海德克(Hitek) 672降傾點劑。完成混合物過 夜冷至塞溫以生成膠凝產品。 例2 除了不加入克勞頓(Kraton) G1701外,其餘皆照例1之步 驟。 例3(比較例) -14 - — 11....--1 I I I «ι yi-. I .1—1. I I . — . . 一 ------ _ 本紙張尺度通用中國國家標準(CNS ) A4规格(210X 297公釐) ---_------^裝------訂------f (讀先閱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(12) 除了不加入聚丁烯32外,其餘皆照例1之步驟。 例4(比較例) 除了不加入聚丁烯32及克勞頓(Kraton) G 1701外,其餘皆 照例1之步驟。 例5 在如例1裝置之樹脂燒瓶中加入254.43克之得利_卡 (Drakeol)500 油、169.62克之聚丁烯 32、10克之克勞頓(Kraton) G 1701、7.59克硬脂酸(酸値爲205.60)及42.38克佛普(Rhone-Poalenc)公司出品之科拉克(Kolate)6054 (5.3%銘)。氮氣可進 入燒瓶中且溫度加熱至100°C。加入9.99克苯曱酸,溫度增 至125°C保持20分鐘。因此,再在49分鐘内溫度增至190°C。 氮氣氛下攪拌並保持溫度8分鐘。在17分鐘内混合物溫度冷 至130°C。再加入5克索伊諾(Irganox) 1035及1克之海德克 (Hitek) 672降傾點劑。完成混合物過夜冷至室溫以生成膠凝 產品。 例6 在如例1裝置之樹脂燒瓶中加入258.81克之得利卡 卬^1^〇1)500油、172.54克之聚丁烯32、10克之克勞頓(Kraton) G1701。氣氣可進入燒瓶中且加入21.26克十四酸(酸値爲 246.50)。攪拌形成混合物同時加熱至100°C之溫度。點滴加 入10.09克三異丙氧化三鋁(12.5%鋁)。加入11.22克苯甲酸, -15 - 尽紙張尺度適用中國國家標準(〇犯)/、4^^(210乂297公釐) (請先閱讀背面之注意事項再填寫本頁) 装· 訂 A7 B7 五、發明説明(13 ) 溫度增至124 C,且再點滴加入10.09克三異丙氧化三鋁。再 在49分鐘内溫度增至190°C。氮氣氛下攪拌並保持溫度8分 鐘。在17分鐘内混合物溫度冷至130°C。加入5克索伊諾 (Irganox) 1035及1克之海德克(Hitek) 672。完成混合物過夜冷 至室溫以生成膠凝產品。 例7 在如例1裝置之樹脂燒瓶中加入267.30克之得利-卡 (0^1^〇1)500、178.20克之聚丁晞32及5克之克勞頓(Kraton) G1701。氮氣可進入燒瓶中且加入19.49克硬脂酸(酸値爲 205.60)。攪拌形成混合物同時加熱至100°C之溫度。點滴加 入7.72克三異丙氧化三鋁(12.5%鋁)。加入8.58克苯甲酸,溫 度增至124°C,且再點滴加入7.72克三異丙氧化三鋁。再在 49分鐘内溫度增至190°C。氮氣氛下攪拌並保持溫度8分鐘。 在17分鐘内混合物溫度冷至13 0°C。加入5克索伊諸(Irganox) 1035及1克之海德克(Hitek) 672。完成混合物過夜冷至室溫以 生成驿凝產品。 這些例子中每一形成凝f·配方之性質總結如下表1。 (請先閱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 -16 - 本紙張尺度適用中國國家榡牟(CNS ) A4说格(210X297公釐) 五、發明説明(14 ) A 7 B7 經濟部中央橾準局員工消費合作社印製 降服點 (巴)* 00 r-H 00 m Os ί—Η t/Ί 鬆弛時間表 〇 t Ο 618 Ο 474 CN 294 FA/BA4 T~H 、 i—Η 、 黏度(厘泊)3 ο ο r-H σΓ CO Ο ο 卜 ίΝ 28,200 23,600 o o rs 〇" 寸 22,350 cn cs <N 滲出於 65C(%) 寸 ο 12.0 CN ΟΊ 17.7 00 o 00 寸 橡膠防滲劑 % (Ν Ο (N Ο CN CN 油/PB1 60/40 60/40 100/0 1 _1 100/0 60/40 60/40 60/40 %皂 卜 \〇 鋁來源 三異丙氧 化三鋁 三異丙氧 化三鋁 »k 'Ί 'Ί ^ 三異丙氧 化三鋁 科拉克 6054 吃墙 st 'Ί '丨1安 β墙 丨'1与 總酸:鋁 莫耳比率 <Ν (Ν (Ν (Ν (N ¥ Τ—Η 2 對照例 4 對照例 卜 韶.埏=V s^怒迴=VPH· 1 ι,#/ο(Ν“φ鉍革ΓΟ 10卜10®%1ί·ζ (Νε 翁h鉍=9ρηί 本紙張尺度適用中國國家標準(CNS ) A4規格(210X2974釐) (請先閱讀背面之注意事項再填寫本頁) 裝· --
J Λ ΑΊ ΑΊ 經濟部中央標準局員工消費合作社印製 五、發明説明(15) 例1 ' 3、5、6及7中之每一凝膠配方可用於此間所述一或 多電彳s装置器材中作爲保護性充填组合物。與聚矽氧基脂 比較,本配方在這些應用上提供相等表現在但費用上則節 省甚多。 例如’其具較低降服點,即5或更少,可更合適用於在組 合物上產生較小應力之裝置,如接線盒或電話埠。對在組 合物上產生較大應力之裝置言,則需較高降服點之配方.。 習知此技藝者可對所欲用途選定合適配方。 改變銘複良中脂肪酸成份對膠凝油之黏度之影響如示於 表1。表1中’脂肪酸··苯曱酸之莫耳比爲1,而總酸比鋁之 莫耳比爲2。油成份對聚丁晞防渗劑之比率爲6 : 4。 如示於表1,令人驚訝於例6中,相對於例1及5而言,減 少脂肪酸之鏈長控制了因增加良含量及/或防滲劑量而黏度 升高的趨勢。例6中同時令人驚訝的發現説明了鏈長小量的 減少大幅降低了膠凝油之降服點及鬆弛時間。 在上述諸例中,黏度是以布非(Brookfield)錐盤黏度計dv-Π型依其操作説明在切變率爲20/秒-1下測得。降服點之衡量 爲頻率爲1赫茲於巴林(Bohlin)VOR流變計測得儲存係數 爲應變之函數而得。由G1對應變之圖中,以技藝中習知方 法計算臨界應變(超過該値則G値即下降)。降服點之衡量即 爲將臨界應變乘以當應變値小於臨界値時G之平均値。 鬆弛時間之決定爲當應變小於臨界應變(如上定義)時衡 量於巴林(Bohlin)VOR流變計測得凝膠應力之鬆弛。在這些 -18 - __本紙張尺度適用中國國家標準(CNS ) A4規格(210X 公釐) I - I 1 -11 HH ^ K I -- - .^^1. 一 N (請先閱讀背面之注意事項再填寫本頁) B7 五、發明説明(16) 測試中,頻率爲i赫茲,在測試中,儲存係數⑹)爲時間函 數加以記錄。鬆弛時間則當G,達到下値: (_G’M 始 ϋ_、 „ , e )e即自然對數的底 :v»· 紙渗測試如下述: 準備物件: 1. 5毫升注射器 一 2.徑寬11公分,1號濾紙 3.派熱斯(Pyrex)視玻璃(直徑12公分) 4. 600毫升派熱斯(pyrex)燒杯 5.實驗室刮勺 6.分析天平 7.鑷子 8.剪刀 9.設在65°C之強制通風爐 步驟: 經濟部中央標準局員工消費合作社印製 1.將脂化合物以刮勺裝入注射器内,緩慢壓下注射栓塞以 去除氣泡。 2.剪下1英吋見方正方形濾紙;稱重(重量i)加以紀錄(至 0.0001克)。 3.缓慢擠出注射器内1毫升化合物至正方形濾紙上成圓狀附 著(在周圍留下空隙以讓附著擴散),測量此,,樣本正方形,, -19 - 本紙張尺度通用中國國家標準(CNS ) A4規格(210X 297^* ) 2^18〇
五、發明説明(i7) 紀錄即重量2。 4. 稱重η公分直徑圓形濾紙(重量3)且置於視玻璃上,將"樣 本正方形"放於濾紙正中央用6〇〇毫升燒杯蓋上。 5. 將樣品在室溫下放置不動i 6小時。 6. 將"樣本正方形"(重量2A)及大圓形濾紙(重量3A)稱重。 7. 更換燒杯下"樣本正方形",且將整组置於爐上不動%小 時。 8. 由爐上移走讓其在大理石表面冷卻5分鐘,將"樣本正方 形·,(重量2B)及大圓形濾紙(重量2B)稱重,注意任何顏色 變化。 9. 丟棄樣本正方形及〉慮紙。 10. 只以鑷子處理樣本正方形及圓形濾紙,避免任何濕氣及 異物沾染上樣本正方形。 計算 1.原始重量=(重量1)-(重量2) 2·重量損失=(重量2)-(重量2A或2B) 3. 重量損失%= 重量損失X 100/原始重量 4. 濾紙重量增加= (重量3A或3B)-(重量3) 5. 揮發重量= a.重量損失-濾紙重量增加(若大於零) b· 〇 ’若重量損失-濾紙重量增加小於等於零 6. 揮發重量% = -20 - 本紙張尺度適用中國國家榡隼(CMS ) A4規格(210X 297公釐) -HI fn . ~1上衣-- (請先閱讀背面之注意事項再填寫本頁) 訂 經濟部中央標準局員工消費合作社印裝 A7 A7 經濟部中央樣準局員工消費合作袄印製 五、發明説明(18 揮發重量X 100/原始重量 7.非揮發性分離〇/〇= 重量損失%-揮發重量% A値爲用以計算室溫16小時後之重量變化,b "値爲用以 計算在65°C再24小時後之重量變化。 測量誤差 因反覆使用樣品’某些測量誤差是可預期的,特別是在 计算室溫之揮發重量,所有重量必須記至〇 〇〇〇1克。所有計 算結果必須記錄至最近整數。每一衡量化合物至少需有三 個樣品同時測試。結果百分比値則加以平均以決定重量損 失%及非揮發性分離%。 下列諸例顯示使用本發明膠凝油充填组合物之罩殼及裝 置的抗濕氣及抗腐蝕性。 例8 將三片分接點置於使用依本發明例5膠凝油配方(但以1〇0/< 皂成份且無防滲劑)之罩殼内。這些分接點包含導電環及導 電片’且浸入溫度介於65下(185°Cg8〇T(26 5。〇),之自來 水中直至深24至30英吋。在導電環及導電片中保持48伏特 直泥電壓14天。裝置之電阻在丨小時後測量,而後每天測 量。在測試結束時’以1〇〇伏特直流電屢:量得電線間電阻超 邊。並無水份滲過罩殼内7/8吋膠凝油。 例9 -21 - 本紙張尺度賴中_家標丨(eNS } A4^^( 21()x297_ n^i ι^ϋ HI— n) n^— I 4 u i ml .^1^1 mu-*< (請先閱讀背面之注意事項再填寫本頁) A7
經濟部中央標準局員工消費合作社印製 將使用例8中膠凝油配方製得之分接點承受例8中詳述條 件42天久。再次以1〇〇伏特直流電壓量得電線間電阻超過 歐姆。 例10 將使用例8中膠凝油配方製得之分接點承受例8中詳述條 件42天久。其次以50伏特直流電壓、1〇〇伏特直流電壓及 伏特直流電壓量得電線間電阻超過1 〇8歐姆。 例11 1吋長0.25吋徑銅管浸入5%氣化鈉溶液中3〇天。其一樣品 塗佈有例8之膠凝油,同時其中二樣品皆塗佈具與膠凝油相 似降服點、強度及黏度之不同商用氧化碎礦物油脂。控制 樣品保留不塗佈。結果顯示本發明膠凝油樣品表現最好, 銅質幾無影響。比較下,以商用脂塗佈之兩樣品及未塗佈 之控制组,顯示具黑氧化物形成沉積在大部分銅管外表 上。此顯示本發明膠凝油比其他者較有效。 例12 ' 依本發明例8至10製備六個具有1呎長服務纜線穿經每一 罩殼之一個埠^服務纜線並非依本發明製造。每一條線末 端切斷,浸入兩呎深水中。監視服務纜線間絕緣電阻14 天。雖然六個樣品其中二個失敗了,但失敗並非因爲膠凝 油。相反地,水能滲透入服務纜線内一呎深。因此,12吋 服務纜線提供之保護比7/8吋膠凝油用以密封罩殼的少。 -22 - 本紙0-尺度適用中國國家標準(CNS ) Μ規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) 、,τ A7 B7 五、發明説明(2〇 再者’除了保護電信裝置外,本發明膠凝油充填组合物 可用作包覆或密裝化合物以密封電氣或其他怕水成分以免 潮濕水氣進入。這些組合物可用以取代技藝中先前應用之 軋聚胺酯彈塑體。例如,本發明組合物可用於接線盒測試 埠之電氣連接器而於埠上成防濕密封。再者,電氣接觸測 P車可以探針穿過凝膠而達成。其他相關之本發明紐合物 於保護電氣設施之應用正如熟諳此技藝者可了解者。 —; ^ -衣 訂 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央橾準局員工消費合作社印製 本紙張尺度適用中國國家標進(CNS ) A4规格(21 〇 X 297公釐)
Claims (1)
- Αδ Β8 C8經濟部中央標準局員工消費合作、杜印製 六、申請專利範圍. i/種傳輸電信訊號之物件,其包括至少—條導電金屬線 以傳載電訊號;具電線之電訊導電金屬元件以接收電訊 號;及膠凝油組合物以保護金屬線及元件免受潮濕,該 膠凝油組合物含約40-90%之油成份、約5_5〇%之防渗 劑、及約4-15%之銘複皂,置於外稍及元件之間。 一種製造之物件,其包括電信纜線,該纜線具有環繞核 心之外鞘,其中含有導電金屬網之多束傳載訊息元件, 係位於核心中,及配置於該核心中之膠凝油組合物,置 於元件與外稍之間;置於外鞘及元件間之該膠凝油組合 物含約40-90%之油成份;約5_50%之防滲劑、及約415% 之紹複皂。 一種保護電信裝置之製造物件,其包括由至少兩配件所 形成之罩殼’其中第一配件包含電信裝置,及第二配件 —包含膠凝油組合物,因此當罩殼由配件組合而形成後, 膠凝油組合物會接觸及保護該電信裝置免於潮濕腐蝕; 該膠凝油組合物含約40-90%之油成份、約5_50%之防滲 劑、及約4-15%之鋁複邕。 4·根據、申請專利範圍第1,2,或3項之物件,其中該膠凝油 組合物含約50-75%量之油成份、約25_45%量之防滲劑、 及約6-12%量之鋁複皂。 5.根據申請專利範圍第4項之物件,其中該油成份爲至少 種礦物油' 環烷油、石蠟油或聚-泛缔烴油。 6·根據申請專利範圍第4項之物件,其中該鋁複皂含脂肪 敏及芳族酸之鋁鹽。 2. 3. 本紙張尺;S -24- —:--:-----^ 衣------訂 {請先閲讀背面之注意事項再填寫本頁) 用中 (CNS ) A4規格(21〇χ·;97公釐) ABCD 297180 六、申請專利範圍 7. 根據中請專利範圍第6項之物件,纟中該脂防酸爲至少 種硬月E!酸、癸酸、油酸、十四酸或棕櫚酸,且該芳族 -酸爲至少一種苯甲酸、對-甲苯甲酸、鄰-甲苯甲酸、二 氣苯甲酸、茶甲酸、審曱酸、菲甲酸、菲甲. 酸、蒽醌w羧酸、蒽醌Μ -羧酸或去氫松香酸。 8. 根據申請專利S固第4項之物件,其中該防渗劑爲合成 油、聚合物或其混合物》 9_根據申請專利範圍第8項之物件,其中該合成油爲具有 至高10個碳原子之α _缔烴寡聚物或經聚合之q q之 晞。 10. 根據申請專利範圍第8項之物件,其中聚合物爲至少一 種橡膠嵌段共聚物’包括丁基橡膠、乙晞_丙烯橡膠、 乙烯_丙烯-二聚體橡膠、氣化橡膠或熱塑性橡膠嵌段共 聚物’且其存在量爲組合物重量之0.5至1 〇%。 11. 根據申请專利範圍第1,2或3項之物件,其進一步包含至 少一種降傾點劑,其量在約〇.丨至1〇重量%之間,及抗氧 化劑,其量在約0.1至2重量%之間。 12. 根據申請專利範圍第11項之物件,其中抗氧化劑包含立 體阻礙之酚類化合物,其含硫鏈結。 13. 根據申請專利範圍第4項之物件,其中該膠凝油包含約 50-75°/。量之油成份、約25_45°/〇量之防渗劑、及約8-12%量 之鋁複皂,其中該油成份爲礦物油,且防滲劑爲聚丁 烯。 14. 根據申請專利範圍第1項之物件,其中該金屬線及元件 -25- 本紙張尺度遄用中國國家標率(CNS ) A4規格(210X297公嫠〉 (請先閲讀背面之注意事項再填寫本頁) •u 訂 經濟部中央標準局員工消费合作社印製 申請專利範圍 之導電金屬含銅。 15. 根據申請專利範園第2項之物件,其中該傳載元件之導 電金屬含銅。 16. 根據申請專利範圍第3項之物件,其中該電信物件之導 電金屬含銅。 I7根據申請專利範圍第1項之物件,其中該元件包括接線 盒。 18_根據申請專利範圍第3項之物件,其中一個配件包含分 線盤’且另一配件爲蓋子。 19. 根據申請專利範圍第18項之物件,其中多串服務纜線係 接至該分線盤。 20. 根據申請專利範圍第18項之物件,其中該分線盤包含多 個插銷,其中多串服務纜線係接至每—插銷上且以固定 物件固定於適當位置上。 21. 根據申請專利範圍第3項之物件’其中該物件爲電話 箱、絕緣卸除連接器、直路分線箱或縮小接線盒。 22. 根據申請專利範圍第!項之物件,其中該物件爲接線 盒。 IJH —*'------f 衣------訂 (請先閲讀背面之注意事項再填寫本頁} 經濟部中央標準局員X消費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)
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| US3791972A (en) * | 1972-01-13 | 1974-02-12 | Southwest Petro Chem Inc | Lubricating grease |
| US3776846A (en) * | 1972-09-08 | 1973-12-04 | Gulf Research Development Co | Aluminum complex soap grease |
| DE2946027C2 (de) * | 1979-11-14 | 1982-05-06 | Siemens AG, 1000 Berlin und 8000 München | Längswasserdichtes Lichtwellenleiterkabel und Verfahren zu seiner Herstellung |
| US4324453A (en) * | 1981-02-19 | 1982-04-13 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| AU571557B2 (en) * | 1983-08-11 | 1988-04-21 | Dainichi-Nippon Cables Ltd. | Waterproof optical fibre cable |
| US5050959A (en) * | 1984-09-10 | 1991-09-24 | Sal Randisi | Fiber optic compositions and method for making thereof |
| GB8429878D0 (en) * | 1984-11-27 | 1985-01-03 | Bicc Plc | Gelled oil filling compounds |
| US4701016A (en) * | 1985-01-31 | 1987-10-20 | American Telephone And Telegraph Company, At&T Bell Laboratories | Thixotropic grease composition and cable comprising same |
| US4787703A (en) * | 1985-10-16 | 1988-11-29 | Uniroyal Chemical Company, Inc. | Cable containing epoxy-modified encapsulation composition |
| US4997720A (en) * | 1987-03-31 | 1991-03-05 | Dexter Corporation | Thermoplastic compositions and articles made therefrom |
| JPH02141810U (zh) * | 1989-01-05 | 1990-11-29 | ||
| US4943685A (en) * | 1989-03-17 | 1990-07-24 | Commu-Tec, Inc. | Cable splicing and termination system |
| JP2819687B2 (ja) * | 1989-11-01 | 1998-10-30 | 住友電気工業株式会社 | 光ケーブル |
| JP2844099B2 (ja) * | 1989-12-26 | 1999-01-06 | 日本石油化学株式会社 | 防水型光ファイバーケーブル |
| US5358664A (en) * | 1992-10-15 | 1994-10-25 | Caschem, Inc. | Gelled oil compositions |
-
1994
- 1994-10-24 US US08/327,726 patent/US5574257A/en not_active Expired - Fee Related
-
1995
- 1995-10-20 AU AU42314/96A patent/AU4231496A/en not_active Abandoned
- 1995-10-20 WO PCT/US1995/014393 patent/WO1996013324A1/en not_active Ceased
- 1995-12-18 TW TW084113516A patent/TW297180B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| US5574257A (en) | 1996-11-12 |
| WO1996013324A1 (en) | 1996-05-09 |
| AU4231496A (en) | 1996-05-23 |
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