TW201039677A - Method for making planar heater - Google Patents
Method for making planar heater Download PDFInfo
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- TW201039677A TW201039677A TW98114587A TW98114587A TW201039677A TW 201039677 A TW201039677 A TW 201039677A TW 98114587 A TW98114587 A TW 98114587A TW 98114587 A TW98114587 A TW 98114587A TW 201039677 A TW201039677 A TW 201039677A
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- carbon nanotube
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- heat source
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- surface heat
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Abstract
Description
201039677 六、發明說明: 【發明所屬之技術領域】 本發明涉及-種輸源’尤其涉及—縣於奈米碳管的面執 源。 ' 【先前技術】 熱源在人們的生產、生活、科研中起著重要的作用。面熱源 係熱源的-種。面熱源為二維結構,將待加熱物體置於該二維社201039677 VI. INSTRUCTIONS OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to a source of the invention, and particularly relates to the surface of the county in the carbon nanotubes. [Prior Art] Heat sources play an important role in people's production, life, and research. The surface heat source is a type of heat source. The surface heat source is a two-dimensional structure, and the object to be heated is placed in the two-dimensional society.
Ο 構的上方對碰進行域,因此,面_可雌加熱物體的各= 部位同時加熱,加熱面較Α、加熱均勻且效輪高。面熱源已成 功用於工業領域、科研領域或生活領域等,如電加熱器、電熱毯、 紅外治療儀及電暖器等。 、 先前面熱源一般包括一加熱元件和至少兩個電極,該至少兩 個電極設置於該加熱元件的表面,並無域元件電連接。當通 過電極向加熱元件通人或電流時,由於加熱元件具有較:電 阻,通入加熱元件的電能轉換成熱能,並從加熱元件釋放出來。 現在市售的面熱源通常採用金屬絲或碳纖維製成的電熱絲作為加 熱元件進行電熱轉換。 然而,金屬絲或碳纖維均具有強度不高、電熱轉換效率較低 及=質較大的缺點。金屬絲易於折斷,特別係多次f曲或繞折成 疋角度t易產生疲勞’因此應用受到限制。$,以金屬絲或碳 纖、准裝成的電熱絲所產生的熱量係以普通波長向外輕射的,其電 熱,換效率不高不利於節省能源,需加人健有遠紅外塗料的棉 線提高電熱轉換效率,不利於節能環保。錢維及金屬絲的品質 均較大’不嫩使麟_化。_,碳麟尺寸不夠小,不利 3 201039677 - 於應用於微型熱源。 自九十年代初以來’以奈米碳管(請參見Helical microtubules of graphitic carbon,Nature,Sumio Iijima,v〇l ;354, p56(199l))為代表 的奈米材料以其獨特的結構和性質引起了人們極大的關注。近幾 年來,隨著奈米碳管及奈米材料研究的不斷深入,其廣闊的應用 月ίι景不斷顯現出來。范守善等人於2〇〇7年12月19日公開的—件 台灣專利申請第95121702號中公開了一種奈米柔性電熱材料。該 ❹ 電熱材料包括一柔性基體及分散在所述柔性基體中的多個奈米碳 官。該多個奈米碳管以粉末態存在,彼此間結合力很弱,無法形 • 成一具有特定形狀的自支撐結構。將該粉末態的奈米碳管與聚合 •物溶液混合時,該粉末態的奈米碳管極易團聚,從而導致奈米碳 管在基體中分散不均勻。為了避免奈米碳管在聚合物溶液中分散 時的團聚現象…方面’在分散的過程巾需要通過超聲波震逢處 理該奈米碳管與聚合物溶㈣混合物,另一方面,該電熱材料中 奈米碳管的質量百分含量不能太高,僅為〇1~4%。 〇 而且,奈米碳管在經過上述分散處理之後’即使奈米碳管彼 =能夠相互接觸’其結合力也較弱,無法形成—自支撐的奈米 碳管結構。由於奈米碳管含量少,熱電材料的熱響應速度不约快, 電熱轉換效率不夠高’故該電紐料的發熱溫度補高,限制了 其應用誠。另,為了使奈米碳管在液相中分散,製備電孰材料 時,其柔性基體只能選擇聚合物材料,聚合物材料耐熱溫度較低, 此種採用在液相中分散奈米碳管形成電熱材料的方法限制了基體 材料的選擇。 【發明内容】 4 201039677 有嚳於此’提供—種換效率 的面熱源的製備方法實為必要。 4圍幸乂見 一種面熱源的製備方法,其包括:提供 隔形成ϋ極及一第-蝥…… 厌吕'、。構,間 弟一電極與該奈米碳管結構形成電 及提供一基體前驅體,將* 电逆搜 奈米碳管複合結構 肘基奴刖驅體與奈米碳管結構複合, Ο 一種!熱源的製備方法,其包括:提供-奈米碳管結構; 供一基體前驅體,將基體 提 月'j驅體與奈米碳管結構複合,形成一加 =件,及間&形成-第—電極及—第二電極與加熱元件形成 電 ‘―種面飾⑽備方法,魏括町挪:提供-奈米碳管 結構;間誠錢-第-電極及—第二電極與該奈米碳管結構形成 電連接,提供-基體前驅體,將基體前驅體與奈米碳管結構複合, 形成-加熱元件;提供-支撐體包括一反射層形成於支撐體表 面,及將所述加熱元件設置於反射層表面。 ❹ —種聽源的製備方法,其包括以下步驟··提供—奈米碳管 線狀結構;奈米碳管雜結構與所述基體前賴複合,形成 -線狀的絲碳管複合結構;將—個❹倾線狀的奈米碳管複 合結構排細彡成-二維結構的加熱元件;及間隔形成—第一電極 及-第二電極與魏㈣奈米碳管複合結射的絲碳管形成電 連接。 相較於先前技術,該形成自支撐的奈米碳f結構,並將該奈 米碳管結構與基體餘複合軸加熱元件的方法鮮,且争米碳 管在加熱元射的含量可方㈣控制。與絲複合後,該奈米碳 5 201039677 =構仍__峨,職㈣伽㈣的發熱 【實施方式】 以下將結合附圖及具體實施 源。 次明本發明提供的面熱 請參閱圖1及圖2,本發明第 該面熱源10為_维蛀m 也例棱供—種面熱源1〇, 斤川為—維結構,即該面熱源 Ο 〇 也應視為本發明保護的範圍。 概叙構’ 該面熱源10包括一加熱元件16、 極14。·^為-AL 第電極12及一第二電 加熱凡件16與第—電極12及第二電極14電 使所述加熱元件16接通電職减過電流。 ; 社納=、轉16包括—奈米碳管複合結構,該奈米碳管複合 1。匕—基體162及至少一奈米碳管結構164與該基體162複 口具體地’ s亥奈米碳管結構164包括多個孔隙,該基體162的 巧渗透入該奈米碳管結構164的多個孔隙中,從而形成—奈米 =官複合結構。當該基體162的體積較大時,該奈米碳管結構说 设置於基體162中,並被該基體162完全包覆。該加熱元件16為 -層狀結構’具體地’該加熱元件16可為一平面結構或曲面結構。 本實%例中,該基體162為一板狀長方體,該奈米碳管結構164 完全嵌於該基體162中。 該奈米碳管結構164為一自支撐結構。所謂“自支撐結構,, 即该奈米碳管結構脱無需通過一支樓體支撐,也能保持自身特 6 201039677 • 定的形狀。該自支撐結構的奈米碳管結構164包括多個奈米碳管, 該多個奈米碳管通過凡德瓦爾力相互吸引,從而形成一網絡^結 構,並使奈米碳管結構164具有特定的形狀,以形成--體的自 支撐的奈米碳管結構。本實關中,該奈米碳f結構164為二維 面狀或-維線狀結構。由於該奈米石炭管結構164具有自支撑性、, 在不通過支樓體表面支樓時仍可保持面狀或線狀結構。該^碳 管結構中奈米碳管之間具有大量間隙,從而使該奈米碳管結 構164具有大1孔隙,該基體162材料渗入該孔隙中。 所述奈米碳管結構164包括均勻分佈的大量奈米碳管,太米 碳管之間通過凡德瓦爾力緊密結合。該奈米碳管結構164中的太 米碳管為無核有序湖。這裏的鱗絲米碳管的排列方向: 規律,這裏的有序指至少多數奈米碳管的排列方向具有一定規 律。具體地’當奈米碳管結構164包括無序排列的奈米碳管時, 奈米碳管可進-步相繞,該鱗_的奈米碳管形成的奈米 碳管結構⑹各向雜;當絲碳管結構164包括有序排列的奈 〇米碳管時,奈米碳管沿-個方向或者多個方崎優取向排列。該 奈米碳管結構164的做優選為α5奈米〜!絲。該奈米碳管結 構164中的奈米破管包括單壁奈米碳管、妓奈米碳管及多壁夺 米碳管中的-種或多種。所述單壁奈米碳管的直徑為〇5奈米〜% 奈米,所述雙壁奈米碳管的直徑為1Ό奈米〜5〇奈米,所述多壁奈 米破管的直徑為1.5奈米〜50奈米。優選地,所述奈米礙管結構164 包括有序排列的奈米碳管,奈米碳管沿_固定方向擇優取向排 =。可以理解’奈米碳管結構164的熱響應速度與其厚度有關。 在相同面積的情況下’絲碳管結構164的厚度紙,熱響應速 7 201039677 度越f又’反之’奈米石反管結構164的厚度越小,熱響應速度越快。 由於4示米碳吕、結構164由純奈米碳管組成,因此該奈米碳管結 構I64的單位面積熱容小於2灌4焦耳每平方厘米開爾文⑶咖2· K) ’優選地小於1/7><1〇_6焦、耳每平方厘米開爾文。該極小的單位 面積熱容使該奈米碳管結構164具有較快的熱響應速度。 ❹ ❹ 二體地D亥奈米碳管結構164包括至少一奈米碳管膜、至少 -奈米碳管線狀結構或所述奈米碳管膜和線狀結構組成的複合結 構可以理解’虽所述奈米碳管結構脱包括多個奈米碳管膜時, 該=奈米碳管膜可層疊設置或併排設置。請參閱圖3,當所述奈 辦餘㈣冑細#_哪個奈米碳管 ⑽行、併排或交又設置成—二維的奈米碳管結構 或二目互纏繞或編織成一二維的奈米碳管結構164。另,請來閱 1-二= 赠結構164可·—奈姆餘結構彎折盤繞 成一、.隹的奈米碳管結構164。 #該奈米碳管魏括奈米碳管拉膜、奈米碳料化 管^膜。該奈米碳管線狀結構可包括至少—個奈米碳管線、、多反 成固21:=平行排列組成的束狀結構或多個奈米碳管線扭轉組 #所述奈米碳管結構164可包括至少—奈米碳管拉膜 碳細中直接拉取獲得的—種具有自二 的不未石厌吕膜。母一奈米碳管拉膜包括多個沿 且:仃於奈米碳管拉膜表面排列的奈米碳管。所述夺^3 凡“爾力首尾相連,以形成一—體 :二 請翏_及圖6,具體地,每一奈米碳管拉膜包;=定 8 201039677 向排列的奈米碳管纽143娜個奈米碳⑻段i43通過凡德瓦 ^首尾相連。每-奈米碳管#段⑷包括多餘互平行的奈米 炭吕145該夕個相互平行的奈米碳管145通過凡德瓦爾力緊密結 合、。該奈米碳管片段143具有任意的寬度、厚度、均勾性及形狀。 所述不米兔官拉膜的厚度為〇5奈米〜1〇〇微米,寬度與拉取該奈 米碳管拉_奈米碳管_的財㈣,長度秘。當該奈米碳 U冓164 &奈米;^管拉膜組成,且奈米碳管結構脱的厚度比 ❹較小時’例如小於10微米,該奈米碳管結構164有很好的透明度, 其透光率可達到90%,可用於製造一透明熱源。 當所述奈米碳管結構164包括層疊設置的多層奈米碳管拉膜 時,相鄰兩層奈米碳管拉膜中的擇優取向排列的奈米碳管之間形 成一交叉角度α’α大於等於〇度小於等於90度(〇。分69〇。)。所 述多個奈米碳管減之間或—個奈米碳管減之巾的相鄰的奈米 碳管之間具有-定間隙,從而在奈米礙管結構104中形成多個孔 隙,孔隙的孔徑尺寸約小於10微米。所述奈米碳管拉膜的具體結 ❹ 構及其製備方法請參見范守善等人於2007年2月12曰申請的, 第96105016號台灣專利申請。為節省篇幅,僅引用於此,但上述 申請所有技術揭露也應視為本發明申請技術揭露的—部分。 本發明實施例的奈米碳管結構164包括多個沿相同方向層疊 設置的奈米碳管拉膜,從而使奈米碳管結構164中奈米碳管均沪 同一方向擇優取向排列。 所述奈米碳管結構164可包括至少一奈米碳管絮化膜,該齐 米石反管I化膜包括相互纏繞且均勻分佈的奈米碳管。奈米碳管白^ 長度大於10微米,優選為200微米~900微米,從而使奈米碳管相 9 201039677 互纏繞在一起。所述奈米碳管之間通過凡德瓦爾力相互吸引、纏 繞’形成網絡狀結構,以形成一個一體的自支撐的奈米碳管絮化 膜。所述奈米碳管絮化膜各向同性。所述奈米碳管絮化膜中的奈 米碳管為均勻分佈’無規則排列,形成大量的孔隙結構,孔隙孔 徑約小於ίο微米。所述奈米碳管絮化膜的長度和寬度不限。請參 閱圖7 ’由於在奈米碳管絮化膜中’奈米碳管相互纏繞,因此該奈 米碳管絮化膜具有很好的柔韌性’且為一自支撐結構,可彎曲折 疊成任意形狀而不破裂。所述奈米碳管絮化膜的面積及厚度均不 限’厚度為1微米〜1毫米’優選為1〇〇微米。所述奈米碳管絮化 膜的具體結構及其製備方法請參見范守善等人於2007年5月11 曰申請的第96116824號台灣專利申請。為節省篇幅,僅引用於此, 但上述申請所有技術揭露也應視為本發明申請技術揭露的一部 分。 所述奈米碳管結構164可包括至少一奈米碳管碾壓膜,該奈 米碳管碾壓膜包括均勻分佈的奈米碳管。所述奈米碳管無序,沿 〇 同—方向或不同方向擇優取向排列。所述奈米碳管碾壓膜中的奈 米碳管相互部分交疊’並通過凡德瓦爾力相互吸引,緊密結合, 使得該奈米碳管結構具雜好的_性,可料折疊成任意雜 而不破裂。且由於奈米碳管礙壓膜巾的奈米碳管之間通過凡德瓦 爾力相互吸引,緊後結合’使奈米碳管礙壓膜為^ —體的自支樓 的結構。所述奈来礙管礙壓膜可通過碾壓一奈米碳管陣列獲得。 所述奈純管棚膜㈣奈米辭_成奈料管_的生長基 底的表面形成-夾角β,其中1大於等於〇度且小於等於15度 (0池I5。)’該夾角β與施加在奈米後管陣列上的壓力有關,壓力 201039677 越大,該夾肖越小,優義’該奈来碳料壓财的奈米碳 行於該生長基底排列。該奈米碳管礙壓膜為通過礙壓一太=# 陣列獲得,依據礙壓的方式不同,該奈米碳管礙壓膜中 管具有不同的排列形式。請參閱圖8,當沿不同方向賴時^2 碳管沿不同方向擇優取向排列。請參閱圖9,當沿同—方向不^ 時’奈米碳管沿-固定方向擇優取向排列。另…料壓方 Ο 〇 直該奈米碳管_表_,該奈米碳”無序排列。該 μ 礙壓膜中奈米碳管的長度大於50微米。 不”反& 該奈米碳管礙賴的面積和厚度不限,可根據實際 擇。該奈料管碾顧的面雜奈米碳管_的尺寸而、 該奈米碳管碾壓膜厚度與奈米碳管陣列的高度及礙 關’可為1微米〜1毫米。可以理解,奈米碳管 施加的壓力越小,·絲碳管賴_厚度越^ ^ 奈米奴官㈣的高度越小而施加_力越大,則 碾壓膜的厚度越小。所述奈米碳管賴膜之中 ,從而在奈米碳管礙歷臈中形成多航隙二 。所述奈米碳管礙壓膜的具她 備方心參見財善等人於2〇〇7年6月29日 號台灣專利申請。為節省篇幅,僅引用於此,但上、' 術揭露也應視為本發明申請技術揭露的一、部分。—&申言月所有技 所述奈米碳管結構164可包括至少 1。,該非扭轉的奈米碳管線二度= 11 201039677 的奈米碳t*。優選地,縣米碳管魏相連。具舰,該非扭轉 的奈米被讀包括翅奈米<管#段,該多個奈米碳管#段通過 凡德瓦爾力首尾相連,每一奈米碳管片段包括多個相互平行並通 過凡德瓦爾力緊密結合的奈米碳管。該奈米碳管片段具有任意的 長度、厚度、均勻性及形狀。該非扭轉的奈米碳管線長度不限, 直徑為0.5奈米-loo微米,优選為1〇微米獅微米 管線的具齡觀製備方絲參紐料等人於職月' 5 曰申請的’於2008年11月21曰公告的台灣專利第13〇3239號, 及於2005年12月16日中請的,於篇年7月i日公開的台灣 專利申請第9414479〇號。為節省篇幅,僅引用於此,但上述^請 所有技術揭露也應視為本㈣申請技術揭露的—部分。The upper surface of the Ο structure is in the domain. Therefore, each part of the surface of the _ female heating object can be heated at the same time, the heating surface is sturdy, the heating is uniform, and the effect wheel is high. The surface heat source has been successfully used in industrial fields, scientific research fields or living areas, such as electric heaters, electric blankets, infrared therapeutic devices and electric heaters. The front front heat source generally comprises a heating element and at least two electrodes, the at least two electrodes being disposed on the surface of the heating element, and no domain elements are electrically connected. When a current or current is passed through the electrodes to the heating element, since the heating element has a relatively: electrical resistance, electrical energy that is passed into the heating element is converted into thermal energy and released from the heating element. Commercially available surface heat sources are usually electrothermally converted using heating wires made of wire or carbon fiber as heating elements. However, both the wire and the carbon fiber have the disadvantages of low strength, low electrothermal conversion efficiency, and large mass. The wire is easily broken, especially if it is repeatedly bent or twisted to an angle t, which is liable to cause fatigue, so the application is limited. $, the heat generated by the wire or carbon fiber, the pre-assembled electric heating wire is lightly emitted from the ordinary wavelength. The electric heat and the low conversion efficiency are not conducive to saving energy. It is necessary to add a cotton wire with far-infrared coating. Improving the efficiency of electrothermal conversion is not conducive to energy conservation and environmental protection. The quality of Qian Wei and the wire are both large. _, carbon collar size is not small enough, unfavorable 3 201039677 - applied to miniature heat sources. Since the early 1990s, nanomaterials represented by carbon nanotubes (see Helical microtubules of graphitic carbon, Nature, Sumio Iijima, v〇l; 354, p56 (199l)) have their unique structure and properties. Has aroused great concern. In recent years, with the deepening of research on carbon nanotubes and nanomaterials, its wide application month ι ι 不断 has been continuously revealed. A nano-flexible electrothermal material is disclosed in Taiwan Patent Application No. 95121702, which is published by the Japanese Patent Application No. 95211702. The ❹ electrothermal material includes a flexible substrate and a plurality of nanocarbons dispersed in the flexible substrate. The plurality of carbon nanotubes exist in a powder state and have a weak bonding force with each other, and cannot be formed into a self-supporting structure having a specific shape. When the powdered carbon nanotubes are mixed with the polymerization solution, the powdery carbon nanotubes are extremely agglomerated, resulting in uneven dispersion of the carbon nanotubes in the matrix. In order to avoid the agglomeration phenomenon when the carbon nanotubes are dispersed in the polymer solution, the 'processed towel needs to be treated by ultrasonic vibration to treat the mixture of the carbon nanotube and the polymer (four), on the other hand, in the electrothermal material The mass percentage of carbon nanotubes should not be too high, only 〇1~4%. 〇 Moreover, after the above-described dispersion treatment, the carbon nanotubes have a weak bonding force even if the carbon nanotubes are in contact with each other, and the self-supporting carbon nanotube structure cannot be formed. Due to the low content of carbon nanotubes, the thermal response speed of thermoelectric materials is not fast, and the electrothermal conversion efficiency is not high enough. Therefore, the heating temperature of the electric materials is increased, which limits its application. In addition, in order to disperse the carbon nanotubes in the liquid phase, when preparing the electro-hydradium material, the flexible matrix can only select the polymer material, and the polymer material has a low heat-resistant temperature, and the dispersing of the carbon nanotubes in the liquid phase is adopted. The method of forming the electrothermal material limits the choice of the matrix material. SUMMARY OF THE INVENTION 4 201039677 It is necessary to prepare a surface heat source for providing a kind of efficiency. 4 Wei Xing see a method for preparing a surface heat source, which comprises: providing a barrier to form a bungee and a first - 蝥 ... 厌吕',. The structure, the electrician-electrode forms electricity with the carbon nanotube structure and provides a matrix precursor, and combines the electro-negative carbon nanotube composite structure elbow-base scorpion and the carbon nanotube structure, Ο one! The preparation method of the heat source comprises: providing a carbon nanotube structure; providing a matrix precursor, compounding the matrix lifter's body and the carbon nanotube structure to form an additive member, and forming an & The first electrode and the second electrode and the heating element form an electric '---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- The carbon nanotube structure forms an electrical connection, providing a matrix precursor, compounding the matrix precursor with the carbon nanotube structure to form a heating element; providing a support comprising a reflective layer formed on the surface of the support, and heating the substrate The component is disposed on the surface of the reflective layer. ❹ a method for preparing a hearing source, comprising the steps of: providing a nanocarbon line-like structure; and the carbon nanotube heterostructure is combined with the matrix to form a linear carbon nanotube composite structure; a heating element having a ❹-lined carbon nanotube composite structure and a two-dimensional structure; and a spacer formed by the first electrode and the second electrode and the Wei (tetra) carbon nanotube The tube forms an electrical connection. Compared with the prior art, the self-supporting nano carbon f structure is formed, and the method of heating the element with the carbon nanotube structure and the matrix residual composite shaft is fresh, and the content of the carbon nanotubes in the heating element is square (4) control. After compounding with the wire, the nanocarbon 5 201039677 = structure still __峨, occupation (four) gamma (four) heat generation [Embodiment] Hereinafter, the drawings and specific implementation sources will be combined. Referring to FIG. 1 and FIG. 2, the surface heat source 10 of the present invention is the heat source 10 of the present invention, which is also a kind of surface heat source 1 〇, and the Kawagawa is a dimensional structure, that is, the surface heat source. Ο 〇 should also be considered as the scope of protection of the present invention. The surface heat source 10 includes a heating element 16 and a pole 14. The ?-AL electrode 12 and a second electric heating element 16 are electrically coupled to the first electrode 12 and the second electrode 14 to cause the heating element 16 to be energized to reduce the current. ; 社 = =, turn 16 includes - carbon nanotube composite structure, the carbon nanotube composite 1 . The substrate 162 and the at least one carbon nanotube structure 164 are overlapped with the substrate 162. Specifically, the Hess carbon nanotube structure 164 includes a plurality of pores, and the substrate 162 is infiltrated into the carbon nanotube structure 164. In a plurality of pores, thereby forming a nano-command composite structure. When the volume of the substrate 162 is large, the carbon nanotube structure is said to be disposed in the substrate 162 and completely covered by the substrate 162. The heating element 16 is a layered structure. Specifically, the heating element 16 can be a planar structure or a curved structure. In the present embodiment, the substrate 162 is a plate-like rectangular parallelepiped, and the carbon nanotube structure 164 is completely embedded in the base 162. The carbon nanotube structure 164 is a self-supporting structure. The so-called "self-supporting structure, that is, the carbon nanotube structure does not need to be supported by a building body, and can maintain its own shape. The self-supporting structure of the carbon nanotube structure 164 includes a plurality of nai The carbon nanotubes, the plurality of carbon nanotubes are mutually attracted by the van der Waals force to form a network structure, and the carbon nanotube structure 164 has a specific shape to form a self-supporting nano-body Carbon tube structure. In this reality, the nano carbon f structure 164 is a two-dimensional planar or -dimensional linear structure. Since the nano-carboniferous tube structure 164 is self-supporting, it does not pass through the surface of the branch building. The planar or linear structure can still be maintained. The carbon nanotube structure has a large amount of gap between the carbon nanotubes, so that the carbon nanotube structure 164 has a large pore, and the matrix 162 material penetrates into the pore. The carbon nanotube structure 164 includes a plurality of carbon nanotubes uniformly distributed, and the carbon nanotubes are tightly coupled by van der Waals force. The carbon nanotubes in the carbon nanotube structure 164 are nuclear-free. Lake. The arrangement of the scales of the carbon nanotubes here: regularity, The order here means that at least most of the carbon nanotubes have a certain regular arrangement direction. Specifically, when the carbon nanotube structure 164 includes a disordered arrangement of carbon nanotubes, the carbon nanotubes can be stepped together. The carbon nanotube structure (6) formed by the carbon nanotubes of the scale_different is heterogeneous; when the carbon nanotube structure 164 comprises an ordered arrangement of naphthene carbon tubes, the carbon nanotubes are in one direction or a plurality of squares Preferably, the carbon nanotube structure 164 is made of α5 nm~! wire. The nanotube in the carbon nanotube structure 164 comprises a single-walled carbon nanotube, a tantalum carbon tube and One or more kinds of multi-walled carbon nanotubes. The diameter of the single-walled carbon nanotubes is 〇5 nm~% nanometer, and the diameter of the double-walled carbon nanotubes is 1 Ό nanometer~5〇 Nano, the multi-walled nanotube has a diameter of 1.5 nm to 50 nm. Preferably, the nano-barrier structure 164 comprises an ordered arrangement of carbon nanotubes, and the carbon nanotubes are fixed along the _ Directional preferred orientation = It can be understood that the thermal response speed of the carbon nanotube structure 164 is related to its thickness. In the case of the same area, the carbon nanotube structure 164 Thickness paper, thermal response speed 7 201039677 Degrees f and 'opposite' The smaller the thickness of the nano stone back tube structure 164, the faster the thermal response speed. Since 4 meters of carbon, the structure 164 is composed of pure carbon nanotubes, Therefore, the carbon nanotube structure I64 has a heat capacity per unit area of less than 2 perfusion of 4 joules per square centimeter of Kelvin (3) coffee 2·K) 'preferably less than 1/7><1〇_6 coke, ear per square centimeter Kelvin. The extremely small heat capacity per unit area allows the carbon nanotube structure 164 to have a faster thermal response speed. ❹ ❹ The two-body D-Hylon carbon tube structure 164 includes at least one carbon nanotube film, at least - nanocarbon The pipeline structure or the composite structure composed of the carbon nanotube film and the linear structure can be understood. 'When the carbon nanotube structure is decoupled from a plurality of carbon nanotube films, the = carbon nanotube film can be laminated. Set or side by side. Please refer to FIG. 3, when the Naiyun (4) 胄 细#_ which carbon nanotubes (10) line, side by side or cross-set and set up - two-dimensional carbon nanotube structure or two-eye intertwined or woven into a two-dimensional The carbon nanotube structure of the honeycomb 164. In addition, please come to read 1-two = gift structure 164 can be - naim structure twisted into a one, 隹 carbon nanotube structure 164. #纳米纳米碳管魏括奈米碳管膜,米碳化化管^膜. The nanocarbon line-like structure may include at least one nano carbon line, a multi-reverse solid 21:= bundle structure in a parallel arrangement or a plurality of nano carbon line torsion group #the carbon nanotube structure 164 It may include at least one of the carbon nanotubes obtained by directly pulling the carbon film in the carbon film. The mother-nano carbon nanotube film comprises a plurality of carbon nanotubes arranged along the surface of the carbon nanotube film. The smashing ^3 凡 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔 尔New 143 Na nano carbon (8) segment i43 is connected end to end by van der Waals. Each - nano carbon tube # segment (4) includes excess parallel parallel nano-carbon 145 该 a parallel parallel carbon nanotube 145 through Devalli is closely combined. The carbon nanotube segment 143 has any width, thickness, uniformity and shape. The thickness of the non-male rabbit film is 〇5 nm~1〇〇micron, and the width is Pulling the carbon nanotubes _ carbon nanotubes _ of the wealth (four), the length of the secret. When the nano carbon U 冓 164 &nanometer; ^ tube tensile film composition, and the thickness ratio of the carbon nanotube structure When the ❹ is small, for example, less than 10 μm, the carbon nanotube structure 164 has good transparency and a light transmittance of 90%, which can be used to manufacture a transparent heat source. When the carbon nanotube structure 164 includes cascading When the multi-layered carbon nanotube film is set, a preferred angle between the adjacent two layers of carbon nanotube film forming a cross angle α is formed between the aligned carbon nanotubes. 'α is greater than or equal to the degree of twist less than or equal to 90 degrees (〇. points 69〇.). The plurality of carbon nanotubes are reduced between or between the adjacent carbon nanotubes of the adjacent carbon nanotubes There is a fixed gap, so that a plurality of pores are formed in the nano-barrier structure 104, and the pore size of the pores is less than about 10 micrometers. The specific structure of the carbon nanotube film and its preparation method can be found in Fan Shoushan et al. The Taiwan Patent Application No. 9610 516, filed on Feb. 12, 2007, is hereby incorporated herein by reference in its entirety, the entire disclosure of the entire disclosure of the disclosure of The carbon nanotube structure 164 includes a plurality of carbon nanotube film laminated in the same direction, so that the carbon nanotubes in the carbon nanotube structure 164 are aligned in the same orientation in the same direction. 164 can include at least one carbon nanotube flocculation membrane comprising carbon nanotubes intertwined and uniformly distributed. The carbon nanotubes have a length greater than 10 microns, preferably 200 microns. 900 micron, thus making the carbon nanotube phase 9 201039677 Intertwined together. The carbon nanotubes are mutually attracted and entangled by a van der Waals force to form a network structure to form an integrated self-supporting carbon nanotube flocculation membrane. The flocculation membrane is isotropic. The carbon nanotubes in the carbon nanotube flocculation membrane are uniformly distributed 'irregularly arranged, forming a large number of pore structures, and the pore diameter is less than about ίο micron. The length and width of the film are not limited. Please refer to Figure 7 'Because the carbon nanotubes are intertwined in the carbon nanotube film, the carbon nanotube film has good flexibility' and A self-supporting structure can be bent and folded into any shape without breaking. The area and thickness of the carbon nanotube film are not limited to 'thickness of 1 micrometer to 1 mm', preferably 1 micrometer. The specific structure of the carbon nanotube film and its preparation method can be found in Taiwan Patent Application No. 96116824, which was filed on May 11, 2007 by Fan Shoushan et al. In order to save space, only the above is cited, but all the technical disclosures of the above application should also be considered as part of the disclosure of the technology of the present application. The carbon nanotube structure 164 can include at least one carbon nanotube rolled membrane comprising uniformly distributed carbon nanotubes. The carbon nanotubes are disordered and arranged in a preferred orientation along the same direction or in different directions. The carbon nanotubes in the carbon nanotube film are partially overlapped with each other and are attracted to each other by the van der Waals force, so that the carbon nanotube structure has a good symmetry and can be folded into Any miscellaneous without breaking. Moreover, since the carbon nanotubes of the nano-carbon tube impede the membrane towel are attracted to each other by the van der Waals force, the structure of the self-supporting building which makes the nano-carbon tube impeding film into a body is combined. The barrier film can be obtained by rolling an array of carbon nanotubes. The surface of the growth substrate of the neat pure tube-film (4) nano-manufactured tube_formation angle_, wherein 1 is greater than or equal to the degree of twist and less than or equal to 15 degrees (0 pool I5.) 'the angle β and application In the pressure on the nanotube array, the larger the pressure 201039677, the smaller the clip, the better the nano carbon of the carbonaceous material is arranged on the growth substrate. The carbon nanotube barrier film is obtained by obstructing the pressure of a too-# array, and the nanotubes have different arrangement patterns depending on the manner of the pressure barrier. Referring to Figure 8, the carbon nanotubes are arranged in different orientations when oriented in different directions. Referring to Figure 9, when the same direction is not the same, the carbon nanotubes are arranged in a preferred orientation along the fixed direction. Another ... material pressure square 〇 straight the carbon nanotube _ table _, the nano carbon" disorderly arrangement. The μ interference film in the length of the carbon nanotubes is greater than 50 microns. No "reverse" the nano The area and thickness of the carbon tube are not limited, and can be selected according to actual conditions. The size of the surface carbon nanotubes of the tube is measured, and the thickness of the carbon nanotube film and the height and the barrier of the carbon nanotube array may be 1 μm to 1 mm. It can be understood that the smaller the pressure exerted by the carbon nanotubes, the more the thickness of the carbon nanotubes is, and the smaller the height of the nano-bureau (four), the greater the thickness of the laminated film. The carbon nanotubes are in the film, thereby forming a plurality of air gaps in the carbon nanotubes. The carbon nanotubes are in the form of a Taiwanese patent application on June 29, 2007. In order to save space, only the above is mentioned, but the above disclosure should also be regarded as one part of the disclosure of the technical application of the present invention. —& 申月月 All Techniques The carbon nanotube structure 164 may include at least one. , the non-twisted nano carbon pipeline second degree = 11 201039677 nano carbon t*. Preferably, the county carbon tube is connected. With a ship, the non-twisted nanometer is read including a winged nano <tube# segment, the plurality of carbon nanotubes # segments are connected end to end by van der Valle force, each nano carbon tube segment comprising a plurality of parallel and The carbon nanotubes are tightly combined by Van der Valli. The carbon nanotube segments have any length, thickness, uniformity, and shape. The length of the non-twisted nano carbon pipeline is not limited, and the diameter is 0.5 nm- loo micron, preferably 1 〇 micron lion micron pipeline, the preparation of the square wire ginseng materials, etc. Taiwan Patent No. 13〇3239, published on November 21, 2008, and Taiwan Patent Application No. 9414479, which was published on December 16, 2005, was published on July i. In order to save space, it is only quoted here, but the above-mentioned ^Please all technical disclosures should also be regarded as part of this (4) application technology disclosure.
該扭轉的奈米碳管線為採用一機械力將所述奈米碳 端沿相反额扭轉麟。職U,雜轉触米碳管線包括 多個繞奈米碳管線軸向螺旋排列的奈米碳管。具體地,該 奈米碳管線包料個奈树料段,鮮個奈米碳以 德瓦爾力首尾相連,每—奈米碳料段包括多個相 ;德==奈米碳管。該奈米碳管片段具有任意的長 “子^/勻域。該扭轉的奈米碳管線長度不限,直徑 為.5不米-100微米,优選為1〇微米-1〇〇微米。 工 進-步地’可採用-揮發性有機溶麟理該扭轉的太 料產生絲祕力的伽下:處理^ 的扭轉的奈h官、㈣相鄰的奈米碳管通過 ^使扭轉的奈米碳峨直徑竭面積減小 12 201039677 由於縣树魏騎財職顧 =::=:r 支_故_ 二 管二::===-個奈米碳 線。另,兮太半石山〜“ 成體的自支撐的奈米碳管 2另1丁"卡石厌&線中相鄰奈米碳管間存在間隙,故該 吕線具有大量孔隙,孔隙的孔徑約小於1〇微米。 丁… 斤述基體162的材料可選擇為高分子材料或無 Ο 〇 162或形成該基體162的前驅體在一定溫度下為^ ==過程中能夠渗透到該奈米碳管結構-的: 複-1 162與奈米碳管結構164相結合的 。該基體162的材料應具有1的耐熱性能 面熱:的4溫度内不致恤壞、變形、熔化、氣化或分解。 的-種:種該=ΓΓ括熱塑性聚合物或熱固性聚合物 2 聚對苯二甲酸“、壓克力_、聚 膠及奸等中二m祕樹脂、環氧樹脂、石夕 材_—種_。本發明實施例中,該基體脱 的材科為環氧樹脂。 隙,圖12 ’由於該奈米碳管結構164令奈米碳管間具有間 料=碳管結構164中形成多個孔隙,且該基體脱或 基體162的前驅體在一定溫度下為液態或氣態,從而使該 ^孔_1、4奈米碳管結構164複合時可滲入該奈米碳管結構164 '、4。圖12為沿平行於奈米碳管拉膜中奈米碳管的排列方 13 201039677 :拉伸4加熱耕16至该加熱元件Μ斷裂後,得到的該加熱元 t16的__ ’可發現,與魏樹脂複合後,該奈米碳管結 冓綱仍能基本保持複合前的形態,奈求碳管在環氧樹脂内基本 沿同一方向擇優取向排列。 絲體162可只填充於所述奈米碳管結構164的孔隙中,也 可如,2所不進一步完全包覆整個奈米碳管結構⑽。請參閱圖 13 ’當該加熱元件16包括多個奈米碳管結構⑽時,該多個奈米 ❹碳管結構⑹可相互間隔(或相互接觸)的設置於該基體162中。 wH碳官結構164為二維結構時’該二維結構可相互間隔或 相互接觸的併排設置或層疊設置在基體162中;當該奈米碳管結 構164為線狀結構時,該線狀結構可相互間隔或相互接觸的設置 在基體162中。當該奈米碳管結構164間隔設置於基體162中時, 可節省製備該加熱元件16所需的奈米碳管結構164的用量。另, 可視實際需要將奈米碳管結構164設置在基體162的特定位置, 從而使該加熱元件16在不同位置具有不同的加熱溫度。 ❹ 可以理解’所述基體162滲透於奈米碳管結構164的孔隙中, 可起到固定該奈米碳管結構164中的奈米碳管的作用,使在使用 時奈米碳管結構164中的奈米碳管不致因外力摩擦或刮劃而脫 落。當所述基體162包覆整個奈米碳管結構164時,該基體162 可進一步保護該奈米碳管結構164。當該基體162為絕緣性的有機 咼分子材料或無機非金屬材料時,該基體162同時保證該加熱元 件16與外部絕緣。另,該基體162可進一步起到導熱及使熱量分 佈均勻的目的。進一步地,當該奈米碳管結構164急劇升溫時, 該基體162可起到缓衝熱量的作用,使該加熱元件16的溫度變化 14 201039677 較為柔和。該基體162的材料可採用柔性高分子材料,從而可增 強整個面熱源10的柔性與韌性。 曰 可以理解,由於該奈米碳管在奈米唆管結構164中均句分佈, 通過將基體162與自支撐的奈米碳管結構綱直接複合形成純 兀件I6,可使奈米碳官在加熱元件10中均勻分佈,且奈求碳 Ο Ο 含量f ’提高了熱源1㈣發熱溫度。由於該奈米碳管結構 164為-自支樓結構,且奈米碳管在奈米碳管結構脱中均句分 佈,將該自支樓的奈米碳管結構164與基體162直接複合,可使 複合後形成的加熱元件16中奈米碳管仍相互結合保持—奈米碳管 結f的形態,從而使加熱元件16中奈米碳管既能均句分佈形 成導電網絡,又不受奈米料在溶液t分散濃度的關,使夺米 碳管在加熱耕16 ”質量百分含量可_ 99%。 ’、 所述第電極I2和第二電極w由導電材料組成該第一電 極Γ t第二電極14的形狀不限’可為導電膜、金屬片或者金屬 引線。優選地,第-電極12和第:電極14均為—層導電膜。舍 用於微型面熱源10時,該導電膜的厚度為0.5奈米〜綱微米; (ΑΤΌ )、導電銀膠、導雷命人你+道+ 士 合的合金。本實施例中,所絲—電極^和第 有5奈米。所述金壯與奈米破管具有較好的 潤濕效果,有·所述第—電極12及第二電極μ 件16之間形成良好的電接觸,減少歐姆接觸電阻。 所述的第-電極12和第二電極14直接與加熱元件16中的奈 15 201039677 電極12和第二電極14間隔 R 10時接入一定的阻值避免 米碳官結構164電連接。其中,第一1 设置,以使加熱元件16應用於面熱源 短路現象產生。 ' 在加熱元件16的表面,從而使寫 米碳管結構164電連接。該第一 加熱元件16的同一表面也可設舊 媒偏 該加熱元件16的基體162尸、填充於該奈米碳管結 構^的孔隙中時,由於該奈米碳管結構脱中部分奈米碳管部 刀水路於加熱元件16表面,該第―電極12和第二電極14可設置 攸而使該苐一電極12和第二電極μ與奈The twisted nanocarbon line uses a mechanical force to twist the nanocarbon end along the opposite direction. The U-turned carbon metering pipeline includes a plurality of carbon nanotubes arranged in an axial spiral arrangement around the carbon nanotube line. Specifically, the nano carbon pipeline is coated with a navel section, and a fresh nanocarbon is connected end to end by Deval, and each nano carbon section comprises a plurality of phases; German == carbon nanotubes. The carbon nanotube fragment has an arbitrary length of "sub-mass". The twisted nanocarbon line is not limited in length and has a diameter of .5 not less than 100 micrometers, preferably 1 micrometer to 1 micrometer. The work-step-by-step-can be used-volatile organic lysate to produce the twisting force of the twisted material: the twisted negron of the treatment ^, the (n) adjacent carbon nanotubes The diameter of the carbon scorpion diameter is reduced by 12 201039677. Because the county tree Wei riding the wealth of the customer ==::=: 支___ Two tubes two::===- a nano carbon line. In addition, 兮 too half stone mountain ~ "The adult self-supporting carbon nanotubes have another gap." There is a gap between the adjacent carbon nanotubes in the line. Therefore, the Lu line has a large number of pores, and the pore diameter of the pores is less than about 1 μm. . The material of the substrate 162 may be selected from a polymer material or a ruthenium-free 162 or a precursor forming the substrate 162 capable of penetrating into the carbon nanotube structure during a certain temperature at a certain temperature: -1 162 is combined with a carbon nanotube structure 164. The material of the base 162 should have a heat resistance of 1 and the surface heat is not deteriorated, deformed, melted, vaporized or decomposed within 4 temperatures. - species: such as = including thermoplastic polymer or thermosetting polymer 2 polyethylene terephthalate", acrylic _, polyglycan and traitor, such as two m secret resin, epoxy resin, Shixi material _ - species In the embodiment of the present invention, the material of the substrate is epoxy resin. The gap, FIG. 12 'Because the carbon nanotube structure 164 has a gap between the carbon nanotubes = a plurality of pores formed in the carbon tube structure 164 And the substrate or the precursor of the substrate 162 is in a liquid state or a gaseous state at a certain temperature, so that the carbon nanotube structure 164 ', 4 can be infiltrated when the hole _1 and 4 carbon nanotube structures 164 are combined. Figure 12 is a view along the arrangement of the carbon nanotubes in the film parallel to the carbon nanotubes 13 201039677: stretching 4 heating tillage 16 to the heating element Μ fracture, the obtained heating element t16 __ ' can be found, After being compounded with Wei resin, the carbon nanotubes can still maintain the morphology before the composite, and the carbon tubes are arranged in the same direction in the epoxy resin. The filaments 162 can only be filled in the naphthalene. In the pores of the carbon nanotube structure 164, it is also possible that, for example, 2 does not completely completely cover the entire carbon nanotube structure. Referring to FIG. 13 'When the heating element 16 includes a plurality of carbon nanotube structures (10), the plurality of nano-carbon tube structures (6) may be spaced apart from each other (or in contact with each other) in the substrate 162. wH carbon When the official structure 164 is a two-dimensional structure, the two-dimensional structures may be arranged side by side or in contact with each other in a matrix 162; when the carbon nanotube structure 164 is a linear structure, the linear structures may mutually The spacers or the mutual contacts are disposed in the base 162. When the carbon nanotube structures 164 are spaced apart from the base 162, the amount of the carbon nanotube structure 164 required to prepare the heating element 16 can be saved. It is desirable to position the carbon nanotube structure 164 at a particular location on the substrate 162 such that the heating element 16 has different heating temperatures at different locations. ❹ It is understood that the substrate 162 is infiltrated into the pores of the carbon nanotube structure 164. The carbon nanotubes in the carbon nanotube structure 164 can be fixed so that the carbon nanotubes in the carbon nanotube structure 164 are not rubbed or scratched by external force during use. Base 162 package The base 162 can further protect the carbon nanotube structure 164 when the entire carbon nanotube structure 164. When the substrate 162 is an insulating organic germanium molecular material or an inorganic non-metal material, the base 162 simultaneously ensures the heating element. The substrate 162 can further serve heat conduction and uniform heat distribution. Further, when the carbon nanotube structure 164 is heated rapidly, the substrate 162 can buffer heat. The temperature change 14 201039677 of the heating element 16 is softened. The material of the base 162 can be made of a flexible polymer material, thereby enhancing the flexibility and toughness of the entire surface heat source 10.曰 It can be understood that since the carbon nanotubes are uniformly distributed in the nanotube structure 164, the carbon element can be formed by directly combining the matrix 162 with the self-supporting carbon nanotube structure to form a pure element I6. It is evenly distributed in the heating element 10, and the carbon Ο Ο content f ' increases the heat generation temperature of the heat source 1 (4). Since the carbon nanotube structure 164 is a self-supporting structure, and the carbon nanotubes are uniformly distributed in the carbon nanotube structure, the carbon nanotube structure 164 of the self-supporting building is directly combined with the base 162. The carbon nanotubes in the heating element 16 formed after the composite can still be combined with each other to maintain the shape of the carbon nanotube junction f, so that the carbon nanotubes in the heating element 16 can be uniformly distributed to form a conductive network without being The concentration of the nano-material in the solution t is such that the carbon nanotubes are heated to 16" mass percentage _ 99%. ', the first electrode I2 and the second electrode w are composed of a conductive material. The shape of the second electrode 14 is not limited to a conductive film, a metal piece or a metal lead. Preferably, the first electrode 12 and the first electrode 14 are each a layer conductive film. When used for the micro surface heat source 10, The thickness of the conductive film is 0.5 nm to micron; (ΑΤΌ), conductive silver glue, and the alloy of the lead + electrode + the alloy. In this embodiment, the wire-electrode ^ and the first 5 nm The Jin Zhuang and the nano tube have a good wetting effect, and the first electrode 12 and the second electricity Good electrical contact is formed between the μ members 16 to reduce the ohmic contact resistance. The first electrode 12 and the second electrode 14 are directly connected to the N15 15 in the heating element 16 and the second electrode 14 is spaced apart from the second electrode 14 by R 10 . A certain resistance is entered to avoid electrical connection of the carbon carbon structure 164. The first 1 is provided to cause the heating element 16 to be applied to the surface heat source short circuit phenomenon. 'On the surface of the heating element 16, thereby making the carbon nanotube structure 164 The same surface of the first heating element 16 can also be provided with the old medium biased to the base 162 of the heating element 16 and filled in the pores of the carbon nanotube structure, because the carbon nanotube structure is off A portion of the carbon nanotube portion is watered on the surface of the heating element 16, and the first electrode 12 and the second electrode 14 may be disposed such that the first electrode 12 and the second electrode μ and
★ n六极示、不咴官結構164電連接,該 第-電極12和第二電極14可設置於加熱元件16的基體162中, 並直接與奈米碳管結構164接觸。此時,為使該第一電極12和第 二,極14與外部電源導通,該第一電極12和第二電極14可部分 暴露於加熱元件16之外;或者,該熱源1〇可進一步包括兩條引 〇 '線’分別與該第—電極12和第二電極14電連接,並從該基體162 内部引出。 δ該奈米竣管結構164中奈米碳管有序排列時,優選地,兮 奈米碳管的排列方向沿第一電極12至第二電極14延伸。具體地Υ 田該奈米碳管結構164包括至少一奈米石炭管拉膜時,所述第一電 才亟12及第二電極14設置於該奈米碳管拉膜的兩端,使奈米唉營 技膜中奈米碳管首尾相連從第一電極12延伸至第二電極14。當兮 奈米碳管結構164包括多個平行排列的奈米碳管線狀結構時 電阻絲相似的,該奈米碳管線狀結構雨端分別與該第一電極12^ 16 201039677 第二電極14電連接。 所述的第一雷杌 示)設置於該加熱元件彳14可通過—導魏結劑(圖未 實現第-電極12和第二^ 結構⑹表面’導絲結劑在 時,還可將所述第―電"^ 4:奈求碳管結構164電接觸的同 管結構⑽的表面上 0弟;;電極14更好地固定於奈米碳 可,-電極=第=:^; ΟThe n-pole display and the non-deformation structure 164 are electrically connected. The first electrode 12 and the second electrode 14 may be disposed in the base 162 of the heating element 16 and directly in contact with the carbon nanotube structure 164. At this time, in order to make the first electrode 12 and the second electrode 14 be electrically connected to the external power source, the first electrode 12 and the second electrode 14 may be partially exposed outside the heating element 16; or, the heat source 1 may further include Two lead 'wires' are electrically connected to the first electrode 12 and the second electrode 14, respectively, and are taken out from the inside of the base 162. When the carbon nanotubes in the nanotube structure 164 are sequentially arranged, preferably, the arrangement direction of the carbon nanotubes extends along the first electrode 12 to the second electrode 14. Specifically, when the carbon nanotube structure 164 includes at least one nano-carbon tube, the first electrode 12 and the second electrode 14 are disposed at both ends of the carbon nanotube film, so that The carbon nanotubes in the rice bran process film are connected end to end from the first electrode 12 to the second electrode 14. When the nanotube carbon nanotube structure 164 comprises a plurality of parallel arranged nanocarbon pipeline-like structures, the resistance wires are similar, and the nanocarbon pipeline-like structure rain ends are respectively electrically connected to the first electrode 12^16 201039677 second electrode 14 connection. The first lightning rod is disposed on the heating element 彳14 and can pass through a conductive soldering agent (the surface of the second electrode 12 and the second surface structure (6) is not realized. Said - "Electric" "^ 4: On the surface of the same tube structure (10) in which the carbon tube structure 164 is in electrical contact; the electrode 14 is better fixed to the nanocarbon, and the electrode = the ==^;
其設置目的係為了n 勺⑽構和材料均不限, =此,==== 保護範2Ϊ6的奈未碳管結構164之間形成電接卿在本發明的 源1〇 ♦ 連解_私電源。秘人電源後熱 所 U石反管結構164即可輻射出—定波長範圍的電磁波。 V面熱源1G可财加熱物制表面雜接觸。或者,所述面熱 源10可與待加熱物體相隔一定的距離設置。 …、 本發明實施例中的面熱源1〇在奈米碳管結構16續面積大小 :定時’通過調節電源電塵大小和奈米碳管絲164的厚度,可 輕射出不同波長範_電磁波。具體地H♦碳t結構164可 產生—紅外線練射。魏電_大小-定時,奈《管結構164 的厚度和面熱源10輻射出電磁波的波長的變化趨勢相反。即當電 源電壓大小一定時,奈米碳管結構164的厚度越厚,面熱源1〇輻 射出電磁波的波長越短;奈米碳管結構164的厚度越薄,面熱源 10輻射出電磁波的波長越長。奈米碳管結構164的厚度一定時, 17 201039677 電源電屢的大小和面熱源1〇韓 米碳管結構164的厚卢 波的波長成反比。即當奈 磁波的波長越短;電^_ _越大’面熱源10_ 越長,理解,該面、二=〇輕射出電磁波的波長 過一電路限制施加在第1電^2應及用=_基體162的材料通 小,使奈米碳管結構16 = 14兩端的電壓大 、、西声鉻囹力η _熱酿度控制在該基體162能耐受的 該基體162的材料為有機高分子聚合物時, ❹ I料t G伏’該面熱源1G的發熱溫度為12此以下,並 ㈣明分子聚合物的炫點。當該基體162的材 10 12〇〇C£^ 圖14 ’本發明實施例通過測量層奈米碳管拉膜相互層 1、的奈米碳管結構脱與環氧樹脂基體脱複合形成的加二 牛16的面熱源10 ’可發現對該面熱源1〇施加電壓越高,該面 熱源10升溫越快,發熱溫度越高。 〇 奈米碳管具有良好的導電性能及熱穩定性,且作為一理想的 黑體結構,具有比較高的熱輻射效率。在另一實施例中,基體^62 採用耐熱材料時,將該面熱源10暴露在氧化性氣體或者大氣的環 境中’其中奈米碳管結構164的厚度為5毫米,通過在1〇伏〜邓 伏調節電源賴,該面熱源1G可输出波長較長的電磁波。通過 溫度測量儀發現該面熱源10的溫度為5(TC〜500。(:。對於具有f體 結構的物體來說’其所對應的溫度為2〇(TC〜45(TC時就能發出人眼 看不見的熱輻射(紅外線)’此時的熱輻射最穩定、效率最高。應 用該奈米碳管結構164製成的面熱源1〇 ’可應用於電加熱器、紅 外治療儀、電熱毯、電暖器等領域。 18 201039677The purpose of the setting is that the n-spoon (10) structure and the material are not limited, = this, ==== the protection of the fan 2Ϊ6 between the n-carbon structure 164 forms an electrical connection in the source of the invention 1 ♦ ♦ _ private power supply . After the secret power supply, the U stone reverse pipe structure 164 can radiate electromagnetic waves in a certain wavelength range. The V-face heat source 1G can be used to make surface contact with the heating material. Alternatively, the surface heat source 10 may be disposed at a distance from the object to be heated. ..., the surface heat source 1 in the embodiment of the present invention has a continuous area of the carbon nanotube structure 16: timing 'by adjusting the size of the power supply dust and the thickness of the carbon nanotube wire 164, the different wavelengths of the electromagnetic wave can be lightly emitted. Specifically, the H x carbon t structure 164 can produce - infrared radiation. Weidian _ size-timing, Nai "the thickness of the tube structure 164 and the change in the wavelength of the electromagnetic wave emitted by the surface heat source 10 are opposite. That is, when the power supply voltage is constant, the thicker the carbon nanotube structure 164 is, the shorter the wavelength of the surface heat source 1 〇 radiates the electromagnetic wave; the thinner the thickness of the carbon nanotube structure 164, the surface heat source 10 radiates the wavelength of the electromagnetic wave. The longer it is. When the thickness of the carbon nanotube structure 164 is constant, the size of the power supply of the 17 201039677 is inversely proportional to the wavelength of the thick Lubo of the surface heat source 1 〇 Han carbon tube structure 164. That is, the shorter the wavelength of the magnetic wave is, the longer the electric ^_ _ is, the longer the surface heat source 10_ is, the longer the wavelength of the electromagnetic wave is exceeded by the circuit, and the second circuit is applied to the first circuit. The material of the base 162 is small, so that the voltage of the carbon nanotube structure 16 = 14 is large, and the west chrome enthalpy η _ thermal brewing is controlled by the substrate 162 which can be tolerated by the substrate 162. In the case of a molecular polymer, the heating temperature of the surface heat source 1G is 12 or less, and (4) the bright point of the molecular polymer. When the material of the substrate 162 is 12 〇〇C£^ FIG. 14 'the embodiment of the present invention is formed by measuring the decarburization of the outer layer of the carbon nanotube film and the decarburization of the epoxy resin matrix. The surface heat source 10' of the two cattle 16 can be found that the higher the applied voltage of the heat source 1 对该 on the surface, the faster the temperature rise of the surface heat source 10, and the higher the heat generation temperature. 〇 Nano carbon tube has good electrical conductivity and thermal stability, and as an ideal black body structure, it has relatively high heat radiation efficiency. In another embodiment, when the substrate 62 is made of a heat resistant material, the surface heat source 10 is exposed to an oxidizing gas or an atmosphere. The thickness of the carbon nanotube structure 164 is 5 mm, and the pass is at 1 volt. Deng Fu adjusts the power supply, and the surface heat source 1G can output electromagnetic waves with longer wavelengths. The temperature of the surface heat source 10 was found to be 5 (TC~500 by a temperature measuring instrument. (: For an object having a f-body structure, the corresponding temperature is 2 〇 (TC~45 (TC can be issued) The heat radiation (infrared) that is invisible to the eye is the most stable and efficient at this time. The surface heat source 1〇' made of the carbon nanotube structure 164 can be applied to electric heaters, infrared therapeutic devices, electric blankets, Electric heaters and other fields. 18 201039677
度較小,為的奈件16中奈米碳管結構164的厚 明的有機或無機材料時,冓164 ’且該基體162的材料為透 該面熱源K)的二;=1°為-透明咖。另,當 成時,該面熱源10為—羊;柔性的聚合物材料製 材料的基體162可通10。進一步地’由於該聚合物 編織成不同形狀,对、成各種形狀’且該奈米碳管線可 服、取暖手套或取;鞋等的面熱源1G可用於製造自發熱的取暖 該面及圖16’本發明第二實施例提供-種面熱源2〇, 談加Γΐ 加熱元件一第一電極22及一第二電極24。 U 26包括一基體262及至少一奈米碳管結構264設置於 土體一62卜加熱元件%為一類二維結構,即為一具有一定厚 ^的二維、、’4。具體地’該加熱元件26可為—平面結構或曲面結 忒加熱το件26的奈米碳管結構264與第一電極22及第二電 極24 $連接,麟使㈣加熱树%魏電源從喊過電流。 該面熱源20的結構與第一實施例的面熱源1〇基本相同,其 不同之處在於’該面熱源2〇進一步包括一支撐體28、一熱反射層 27及一保護層25。所述熱反射層27設置於支撐體28的表面。所 述加熱元件26設置於所述熱反射層27的表面。所述第一電極22 和第二電極24間隔設置於所述加熱元件26的表面,並與該加熱 元件26電接觸,用於使所述加熱元件26中流過電流。所述保護 層25設置於所述加熱元件26的表面,用於避免所述加熱元件26 吸附外界雜質。所述支撐體28、熱反射層27及保護層25均為可 選擇結構。進一步地’該面熱源20包括兩條電極引線29,分別與 19 201039677 所述第電極22和第二電極24相連,從嵌於基體262中的第一 電極22和第二電極24引出至基體262外。 所这支樓體28做不限,其具有一表面用於支撐加熱元件16 或者熱反射層27。該表面可為平减曲面。優選地,所述支撐體 2'為一板狀結構’其材料可為硬性材料m、玻璃、樹脂、 英等亦可選擇柔性材料,如:塑膠或樹脂等。其中,支樓體 Ο 〇 28的大小不限’可依據實際需要進行改變。本實施織選的支撐 體28為一陶瓷基板。 ",”、、射層27的設置用來反射加熱元件26所發的熱量, 從而控制加熱的方向,麟單面加熱,並進—步提高加熱的效率。 =述熱反射層27的材料為—白色絕緣材料,如:金屬氧化物、金 屬鹽或陶料。本實_中,熱反騎27為三氧化二_,其厚 ^為100微米〜G.5絲。該熱反射層27可通過濺射或其他方法形 支表m轉,所賴反縣27也可設置在 : 退加熱兀件26的表面,即所述支樓體28設置於所述 ==26和所述熱反射層27之間。所述熱反射層27為一可選 瞎而I。所返加熱元件26可直接設置在支禮體28的表面,此 時面…源10的加熱方向不限,可用於雙面加熱。 娜所^護層25為—可選擇結構,其材料為—絕緣材料,如: 』膠、橡膠或樹脂等。所述保讀 選摆。所、a 25厚度祕,可贿實際情況 熱元件W,本實姆,該罐 t 谬,其厚度為0.5〜2毫米。·糾心 卿+為耐熱橡 献1 蔓層可保護加熱元件%,尤 …該加熱轉26懷施僅填充於奈米碳管結細的孔隙 20 201039677 =可防止,加熱元件26表面的奈米碳管受 及=電極24外與外部亥加熱兀件26除所述第一電極22 源30包括1本發明第三實施例提供—種面熱源30,該面埶 二維結構。具體地, ❹ Ο -電極32及第二電極34電連接,用熱疋件%與第 米碳管接物從而流繼。用於使所杨熱元件对的奈 不同SO的結構與第一實施例的面熱源10基本相同,其 施。該多個夺乎包括多個奈米碳管線狀複合結構 元件36 $太伞灭^線複5結構366相互編織形成二維的加熱 與-基體#線狀複合結構366為將—奈米碳管線狀結構 的孔降中兮仔到。該基體材料填充於該奈米碳管線狀結構 祕狀的加熱碰36。該紐材料優選為祕的聚合物。 其包==本瓣_赌i咖㈣製備方法, 步驟-’提供一奈米碳管結構164,該奈米礙管 多個孔隙。 根據奈米碳管結構164的不同,所述奈米碳管結構脱的製 備方法包括:直接_法、賴法、絮化轉。林施例中,节 奈米碳管結構偷可為-維結構也可為二維結構。下面將對上述 幾種奈米碳管結構I64的製備方法進行分別敍述。 21 201039677 該 ㈠當該奈米碳管結構包括至少一奈米碳管拉膜 奈米碳管結構的製備方法具體包括以下步驟: 、 首先,提供一奈米碳管陣列形成於一生長基底,該陣列為超 順排的奈米碳管陣列。 巧超When the degree is small, it is a thick organic or inorganic material of the carbon nanotube structure 164, and the material of the substrate 162 is two of the surface heat source K; =1° is - Transparent coffee. Further, when formed, the surface heat source 10 is - sheep; the base 162 of the flexible polymer material can pass 10. Further, 'the polymer is woven into different shapes, paired into various shapes' and the nanocarbon pipeline can be taken, heated gloves or taken; the surface heat source 1G of shoes and the like can be used to manufacture the self-heating heating surface and FIG. 16 The second embodiment of the present invention provides a seed surface heat source 2, a heating element, a first electrode 22 and a second electrode 24. U 26 includes a base 262 and at least one carbon nanotube structure 264 disposed on the soil body 62. The heating element % is a two-dimensional structure, that is, a two-dimensional, '4 having a certain thickness ^. Specifically, the heating element 26 may be a planar structure or a curved surface heating device 264. The carbon nanotube structure 264 is connected to the first electrode 22 and the second electrode 24 $, and the lining (4) heats the tree. Overcurrent. The surface heat source 20 has substantially the same structure as the surface heat source 1 of the first embodiment, except that the surface heat source 2 further includes a support body 28, a heat reflection layer 27, and a protective layer 25. The heat reflective layer 27 is disposed on the surface of the support body 28. The heating element 26 is disposed on the surface of the heat reflective layer 27. The first electrode 22 and the second electrode 24 are spaced apart from the surface of the heating element 26 and are in electrical contact with the heating element 26 for flowing a current through the heating element 26. The protective layer 25 is disposed on the surface of the heating element 26 for preventing the heating element 26 from adsorbing foreign matter. The support body 28, the heat reflecting layer 27, and the protective layer 25 are all optional structures. Further, the surface heat source 20 includes two electrode leads 29 connected to the first electrode 22 and the second electrode 24 of 19 201039677, respectively, and drawn from the first electrode 22 and the second electrode 24 embedded in the base 262 to the base 262. outer. The building body 28 is not limited and has a surface for supporting the heating element 16 or the heat reflecting layer 27. The surface can be a reduced surface. Preferably, the support body 2' is a plate-like structure, and the material thereof may be a hard material m, glass, resin, or the like, or a flexible material such as plastic or resin. Among them, the size of the branch body Ο 28 is not limited, and can be changed according to actual needs. The support 28 selected for this embodiment is a ceramic substrate. ",", the layer 27 is arranged to reflect the heat generated by the heating element 26, thereby controlling the direction of heating, heating the single side of the lining, and further improving the efficiency of heating. The material of the heat reflecting layer 27 is - white insulating material, such as: metal oxide, metal salt or ceramic material. In the present, the thermal anti-riding 27 is a trioxide, and its thickness is 100 micrometers to G.5 filaments. The heat reflective layer 27 can be The surface of the meter can be rotated by sputtering or other methods, and the anti-county 27 can also be disposed on the surface of the heat-removing element 26, that is, the branch body 28 is disposed on the ==26 and the heat-reflecting layer. The heat reflecting layer 27 is an optional cymbal. The heating element 26 can be directly disposed on the surface of the ceremonial body 28, and the heating direction of the surface 10 is not limited, and can be used for two sides. Heating. Na's protective layer 25 is - optional structure, the material is - insulating material, such as: "glue, rubber or resin, etc.. The reading of the pendulum. A 25 thickness secret, can be bribed actual heat Component W, Ben Sum, the tank t 谬, its thickness is 0.5~2 mm. · Correction Qing + for the heat-resistant rubber 1 vine layer can protect the heating element %, especially... The heating turn 26 is only filled in the pores of the carbon nanotubes. 20 201039677 = can prevent the carbon nanotubes on the surface of the heating element 26 from being affected by the electrode 24 and the external heating element 26 The source 30 of the first electrode 22 includes a surface heat source 30 provided by the third embodiment of the present invention, and the surface is two-dimensionally structured. Specifically, the ❹-electrode 32 and the second electrode 34 are electrically connected, and the heat-generating member is used. % and the carbon nanotubes are connected in sequence. The structure of the different SOs used to make the pair of heat elements is substantially the same as that of the surface heat source 10 of the first embodiment, and the plurality of The rice carbon line-like composite structural element 36 is too umbrella-killed and the double-structured 366 is woven to form a two-dimensional heating and-base body. The linear composite structure 366 is a hole in which the carbon nanotube-like structure is lowered. The base material is filled with the heat bump 36 of the secret structure of the nano carbon line structure. The material of the material is preferably a secret polymer. The package == the present flap _ gamma i (four) preparation method, the step - 'provide one The carbon nanotube structure 164, which interferes with a plurality of pores. According to the difference of the carbon nanotube structure 164, The preparation method of the carbon nanotube structure decoupling includes: direct_method, Lai method, flocculation conversion. In the forest application example, the carbon nanotube structure can be a dimensional structure or a two-dimensional structure. The preparation methods of the above several carbon nanotube structures I64 are separately described. 21 201039677 The method for preparing the carbon nanotube structure including at least one carbon nanotube-coated carbon nanotube structure comprises the following steps: First, an array of carbon nanotubes is provided on a growth substrate, which is a super-aligned array of carbon nanotubes.
該奈米碳管陣_製備妓_化學氣減積法,其具體步 驟包括.(a)提供-平整生長基底,該生絲底可顧p型或n 型石夕生長基底’或形成有氧化層⑽生絲底,本發明實施 例優選為_ 4射的料錄底;⑻在生絲絲面均句形 成-催化劑層,該催化劑層材料可選用鐵(Fe)、姑(c〇)、錄㈤) 或其任意組合的合金之-;(e)將上聽成有雜”綱的生長基 底在700。〇9貌的空氣中退火約3()分鐘〜%分鐘;⑷將處理 過的生長基底置於反應射’在賴氣體魏下加制肅c C ’然後通入碳源氣體反應約5分鐘〜3〇分鐘,生長得到奈米碳管 陣列。該奈米碳管_為多個彼辭行且垂直於生長基底生長的 奈米碳管形成_奈祕管_。通過上述㈣生長條件,該定 向排列的奈米碳管陣财基林含有㈣,如無定型碳或殘留的 催化劑金屬顆粒等。 本發明實施例提供的奈米碳管陣列為單壁奈米碳管陣列、雙 壁奈米奴營陣列及多壁奈米;ε炭管陣列中的一種。所述奈米破管的 直徑為1奈米〜50奈米,長度為50奈米〜5毫米。本實施例中,奈 米碳管的長度優選為100微米〜9〇〇微米。 本發明實施例中碳源氣可選用乙炔、乙烯、曱烷等化學性質 較活潑的碳氫化合物,本發明實施例優選的碳源氣為乙炔;保護 氣體為氮氣或惰性氣體,本發明實施例優選的保護氣體為氬氣。 22 201039677 n可⑽解,本發咐施鑛㈣奈米碳管陣列秘於上述製 法,也可為石墨電極恒•弧放魏積法、婦蒸發沈積法、 其次 ,採用-拉伸工具從奈米碳管陣财拉取奈米碳管 =、-奈米碳管拉膜,其具體包括以下步驟··(a)從所述超^非 不米碳管陣列中選定—個或具有4寬度的多個奈米碳管,本告 施例優選為制具有1寬度的膠帶、鎖子或夾子接觸夺米碳ίThe carbon nanotube array_preparation 妓_chemical gas debulking method, the specific steps thereof include: (a) providing a flat growth substrate, the raw silk substrate can be p-type or n-type slab growth substrate or forming an oxide layer (10) Raw silk bottom, the embodiment of the present invention is preferably a recording base of _ 4 shots; (8) forming a catalyst layer on the raw silk surface, the catalyst layer material may be selected from iron (Fe), gu (c〇), recorded (5)) Or an alloy of any combination thereof; (e) anneal the growth substrate on the surface of the 700. 〇9 appearance in air for about 3 () minutes to % minutes; (4) place the treated growth substrate After the reaction shot 'adds c c ' under the gas, and then reacts with the carbon source gas for about 5 minutes to 3 minutes, the nano carbon tube array is grown. The carbon nanotubes are a plurality of The carbon nanotubes formed perpendicular to the growth substrate are formed. According to the above (4) growth conditions, the aligned carbon nanotubes contain (4), such as amorphous carbon or residual catalyst metal particles. The carbon nanotube array provided by the embodiment of the invention is a single-walled carbon nanotube array, double-walled nanotube a battalion array and a multi-walled nano; one of the ε carbon tube arrays. The diameter of the nanotube is 1 nm to 50 nm, and the length is 50 nm to 5 mm. In this embodiment, the carbon is used. The length of the tube is preferably from 100 μm to 9 μm. In the embodiment of the present invention, the carbon source gas may be a chemically active hydrocarbon such as acetylene, ethylene or decane. The preferred carbon source gas in the embodiment of the present invention is acetylene. The protective gas is nitrogen or an inert gas, and the preferred shielding gas in the embodiment of the present invention is argon. 22 201039677 n (10) solution, the present invention (4) carbon nanotube array is secreted by the above method, and may also be a graphite electrode • Arc-distribution method, women's evaporation deposition method, secondly, using a -stretching tool to pull the carbon nanotubes from the carbon nanotubes, and the carbon nanotubes are pulled, which specifically includes the following steps: (a) Selecting one or a plurality of carbon nanotubes having a width of 4 from the array of super-non-carbon nanotubes, the present embodiment preferably has a tape, a lock or a clip with a width of 1 contact carbon.
陣列以奴-個或具有-妓度的多個奈米碳管;⑻以」定^ 度拉伸該選糾奈米碳管,從㈣成首尾相連的多個奈米碳管片 &,進而形成-_的奈米碳管I餘取方向沿基本垂直於太 米碳管陣列的生長方向。 、不 在上述拉伸過財’衫贿米碳"段錄力仙下 伸方向逐漸麟生長基朗同時,由於凡德瓦爾力作用,該 的多個奈米碳管諸分顺其他奈米碳K段魏树地連續地 被拉出,從_成-連續、均勻且具有—定寬度的奈米碳管膜。 該奈米碳管魅括多個首尾树的奈米碳管,該奈米碳管基本卜 拉伸方向制。請參_ 5及圖6,該奈米碳管臈包括多個 向排列的奈米碳管145。進-步地,所述奈米碳管膜包括多個 相連且以射财米碳⑼段143,奈米碳料段143兩端通過 凡德瓦爾力相互連接。該奈米碳f片段143包括多個相互平 列的奈米碳管M5。魅錄倾得奈米碳管朗方法簡單 適宜進行工業化應用。 、 該奈米碳管賴寬㈣奈米碳管_的尺寸細,該奈米碳 管膜的長度秘,可根翁際需_得。#該奈米碳管陣二的二 23 201039677 該奈米碳管膜的寬度為〇.5奈米〜10厘米,該夺米 石反官膜的厚度為〇.5奈米〜卿微米。 …卡 ^丰^上述奈料管拉·備奈米碳管結構164。 還可膜可!為—奈米碳管結構164使用。進-步, Κ^米碳綠醉行無f猶或/和層_設得到一夺 未石厌官結構164。由於該奈米 不 該奈米碳管減具綠A碰 'Λ 4 ®積’因此 .大枯丨生,故多層奈米碳管膜可相互緊密I士 ❹ Ο n, 心丁、水石反®結構164中,奈米碳管拉 、、^ 、目鄰兩層奈米碳管減之間具有-交叉角产α, 赞’具财依射際絲⑽。崎奈鱗㈣可^個 1至另個电極方向鋪設’從而使奈米碳管膜十奈米碳管沿一 個電極至另一個電極方向延伸 αThe array is a slave or a plurality of carbon nanotubes having a twist; (8) stretching the selected carbon nanotubes at a constant degree, and (iv) a plurality of carbon nanotube sheets & Further, the carbon nanotube I forming a -_ direction is along a growth direction substantially perpendicular to the growth direction of the carbon nanotube array. Not in the above-mentioned stretched wealth, 'shirts and bribes, carbon carbon', and Duan Lunli’s extension to the gradual growth of Keelan. At the same time, due to the effect of Van der Waals force, the plurality of carbon nanotubes are divided into other nano carbon K segments. Wei Shudi is continuously pulled out from the _ into a continuous, uniform and has a width of the carbon nanotube film. The carbon nanotubes are surrounded by a plurality of carbon nanotubes of the first and last trees, and the carbon nanotubes are basically oriented in a stretching direction. Referring to _ 5 and FIG. 6, the carbon nanotubes include a plurality of aligned carbon nanotubes 145. Further, the carbon nanotube film comprises a plurality of connected and carbonized carbon (9) segments 143, and the carbon nanotube segments 143 are connected to each other by a van der Waals force. The nanocarbon f-fragment 143 includes a plurality of carbon nanotubes M5 which are parallel to each other. The charm of the nano-carbon tube method is simple and suitable for industrial applications. The carbon nanotubes are wide (four) carbon nanotubes _ small in size, the length of the carbon nanotube membrane is secret, and it can be obtained. #纳米米碳管阵二的二23 201039677 The width of the carbon nanotube film is 〇.5nm~10cm, and the thickness of the glutinous stone anti-official film is 〇.5nm~qing micron. ...卡 ^丰^ The above-mentioned Nai tube pulls the nano carbon tube structure 164. It is also possible to use a film for the carbon nanotube structure 164. In-step, Κ ^ m carbon green drunk without f or / and layer _ set to get a win without stone ugly official structure 164. Because the nanometer does not have a carbon nanotube reduction, the green A touches the 'Λ 4 ® product'. Therefore, the multi-layered carbon nanotube film can be close to each other. I, 心 n, 心, 水石反® In structure 164, the carbon nanotubes of the carbon nanotubes, the ^, and the two adjacent layers of the carbon nanotubes have a cross-angle production of α, and a tribute to the sacred silk (10). The scallop scale (4) can be laid 1 to the other electrode direction so that the carbon nanotube film ten carbon nanotubes extend along one electrode to the other electrode.
本實施例中’進-步包括用有機溶劑處理奈米碳管結構脱 的步驟,該有機溶劑為揮發性有機溶劑,可翻乙醇、甲醇、丙 H乙脉氣仿中-種或者幾種的混合,本實施例中的有機 =劑採用乙醇。該使财機溶織_步驟具體為:將該奈米碳 管結構164設置於-基絲面或—框架結構上,通過試管將有機 各劑滴洛在奈米碳管結構164表面浸潤整個奈米碳管結構⑹,或 者’也可將上述奈米碳管結構164浸入盛有有機溶劑的容器中浸 潤。所述的奈米碳管結構164財機賴制處猶,當夺米碳 管膜的層數較少時,在表面張力的作用下,奈米後管膜^目鄰^ 奈来碳管會收縮賴隔分佈的奈米碳管線。而當奈米碳管膜的層 數較多時,有機溶劑處理後的多層奈米碳管膜為—均勻的膜^ 構。有機溶劑處理後,奈米碳管結構164的粘性降低,更便於I 24 201039677 用。 (二)當該奈米碳管結構164包括至少一奈米碳管絮化膜, 該奈米碳管結構164的製備方法包括以下步驟: 首先,提供一奈米碳管原料。 所述奈米碳管原料可為通過化學氣相沈積法、石墨電極恒流 電弧放電沈積法或鐳射蒸發沈積法等各種方法製備的奈米碳管。 本實施例中,制刀片或其他卫具將上述定向排觸奈米碳 管_從基底刮落,獲得—奈米碳管原料。優親,所述的奈米 碳管原料中,奈米碳管的長度大於1〇〇微米。 其次’將上述奈米碳管補添加到—賴巾並進行絮化處理 獲得-奈米碳管絮狀結構,將上述奈米碳管絮狀結構從溶劑中分 離’並對該奈米碳管練結構定型處朗獲得—奈米碳管膜。 本發明實施射’溶劑可_水、祕發的有機溶劑等。絮 化處理可通過採用超聲波分散處理或高強度授摔等方法。優選 地’本發明實施例採用超聲波分散1〇分鐘〜3〇分鐘。由於奈米碳 ❹管具有極大的比表面積’相互魏的奈米碳管之·有較大的凡 ,瓦爾力。上述絮化處理並不會將該奈米碳f原料中的奈米碳管 &王分散在溶射,奈米碳管之間通過凡德瓦爾力相互吸引、纏 繞’形成網絡狀結構。 本發明實施例中’所述的分離奈米碳管絮狀結構的方法具體 包括以下步驟:將上述含有奈米碳管絮狀結構的溶劑倒入一放有 濾紙的漏斗中;靜置乾燥-段時間從而獲得一分離的奈米碳管絮 狀結構,圖19為該奈米碳管絮狀結構的照片。 本發明實施例中,所述的奈米碳管絮狀結構的定型處理過程 25 201039677 具體包括町步驟:將上述奈米碳f絮狀結構置於—容 結構按照預定形狀攤開;施加—定壓力:攤二 不未反s1狀結構;及’將該奈米碳管絮狀結構中殘留的 乾或等溶編轉發後獲得—絲碳管絮化 - 管絮化膜的掃描電賴片。 _奈米碳 —本發财施例可通触奈米碳管絮狀結構攤 開的面積來控繼奈米碳衫倾的厚度和面密度。奈米碳In the present embodiment, the step further comprises the step of treating the structure of the carbon nanotubes with an organic solvent, which is a volatile organic solvent, which can be turned into ethanol, methanol, propylene, ethyl ethane, or the like. Mixing, the organic agent in this example employs ethanol. The step of dissolving the machine is as follows: the carbon nanotube structure 164 is disposed on the -base surface or the frame structure, and the organic agent is dripped on the surface of the carbon nanotube structure 164 through the test tube. The carbon nanotube structure (6), or 'the above carbon nanotube structure 164 may also be immersed in a container containing an organic solvent to infiltrate. The carbon nanotube structure of the carbon nanotube structure is still in place. When the number of layers of the carbon nanotube film is small, under the action of surface tension, the nano-tube membrane is adjacent to the carbon nanotubes. Shrinking the nano carbon line distributed by the partition. When the number of layers of the carbon nanotube film is large, the multilayered carbon nanotube film treated with the organic solvent is a uniform film structure. After the organic solvent treatment, the viscosity of the carbon nanotube structure 164 is lowered, which is more convenient for I 24 201039677. (b) When the carbon nanotube structure 164 includes at least one carbon nanotube flocculation membrane, the preparation method of the carbon nanotube structure 164 includes the following steps: First, a carbon nanotube raw material is provided. The carbon nanotube raw material may be a carbon nanotube prepared by various methods such as chemical vapor deposition, graphite electrode constant current arc discharge deposition or laser evaporation deposition. In this embodiment, a blade or other implement is used to scrape the above-mentioned aligned carbon nanotubes from the substrate to obtain a carbon nanotube material. Preferably, in the carbon nanotube raw material, the length of the carbon nanotube is greater than 1 〇〇 micrometer. Secondly, the above-mentioned carbon nanotubes are added to the ray towel and subjected to flocculation treatment to obtain a nanocarbon tube floc structure, and the above-mentioned carbon nanotube floc structure is separated from the solvent and the carbon nanotube is The structure is shaped and the position is obtained - the carbon nanotube film. The present invention can be carried out by using a solvent such as water, a secret organic solvent or the like. The flocculation treatment can be carried out by using ultrasonic dispersion treatment or high-strength imparting. Preferably, the embodiment of the invention is ultrasonically dispersed for 1 minute to 3 minutes. Since the nano-carbon nanotubes have a very large specific surface area, the mutual-neutral carbon nanotubes have a larger, Valli force. The above flocculation treatment does not disperse the carbon nanotubes and the king in the nanocarbon f raw material in the solvent, and the carbon nanotubes are mutually attracted and entangled by the van der Waals force to form a network structure. The method for separating the carbon nanotube floc structure in the embodiment of the present invention specifically includes the following steps: pouring the solvent containing the carbon nanotube floc structure into a funnel with a filter paper; A time is obtained to obtain a separated carbon nanotube floc structure, and FIG. 19 is a photograph of the carbon nanotube floc structure. In the embodiment of the present invention, the shaping process of the nano carbon tube floc structure 25 201039677 specifically includes the step of arranging the above-mentioned nano carbon f floc structure to be spread according to a predetermined shape; Pressure: the second is not anti-s1 structure; and 'the dry carbon fiber or the same solution in the floc structure is transferred to obtain the silk carbon tube flocculation - tube flocculation film scanning electric film. _Nano Carbon - This wealth-raising example can control the thickness and areal density of the carbon nanotubes through the area spread by the nano-carbon tube floc structure. Nano carbon
狀結構攤__越大,_奈米碳管絮傾的厚度和面密声就 越小。本發财關帽得的奈米碳管絮⑽,該奈米碳管= 膜的厚度為1微米_2毫米。 ” ❹ 另’上述分離與定型處理奈米碳管絮狀結構的步驟也可直接 ㈣抽_方式實現,具體包括町㈣:提供—微孔濾膜及一 抽氣漏斗’將上述含有奈米碳管絮狀結構的溶舰過該微孔淚膜 倒入該抽氣漏斗中:減並麟後獲得—奈来碳管絮化膜。^微 孔渡膜為-表面光滑、孔縣㈣微米的細。由於赠方^本 身將提供—較大㈣該奈米碳管絮狀結構,該奈米碳管 絮狀結構經過抽濾會直接形成—均勻的奈米碳管絮化膜。且,: 於微孔濾膜表面光滑’該奈米碳管絮化膜容易獅,得到一自支 撐的奈米碳管絮化膜。 其請參見圖7,上述奈米碳管絮化膜中包括相互纏繞的奈米碳 &’所述奈米碳管之間通過凡德瓦爾力相互吸引、纟廛繞,形成網 絡狀結構,因此該奈米碳管絮化膜具有很好的韌性。該奈米碳管 絮化膜中’奈米碳管為均勻分佈且無規則排列。 可以理解,該奈米碳管絮化膜的具有一定的厚度,且通過控 26 201039677 制:亥不米灰s絮狀結構攤開的面積及壓力大小可控制其厚度。所 以該奈米碳管絮化膜可直接作為一奈米碳管結構崩使用。另, Γ將至少兩層奈米碳管絮倾層較置或併排設置形成-奈米碳 管結構164。 (三)當該奈米碳管結構164包括至少一奈米碳管礙壓膜, 該奈米碳管結構164的製備方法包括以下步驟: 首先,提供-奈米碳管_形成於—生長基底,該陣列為定 向排列的奈米碳管陣列。 〇 述奈米碳管陣列優選為—超順排的奈米碳管陣列。所述奈 米碳管陣列與上述奈米碳管陣列的製備方法相同。 其次,採用-施壓裝置,擠慶上述奈米碳管陣列獲得一夺米 碳管碾壓膜,其具體過程為: 該施壓裝置施加-定的壓力於上述奈米碳管陣壯。在施壓 的過程中’奈轉管_在壓力的_τ會與线絲分離,從 而形成由多個奈米碳管組成的具有自支撐結構的奈米碳管礙壓 〇膜,且所述❹個奈米碳錄本上與奈米碳細壓商表面平行。 本發明實施例中,施壓裝置為—壓頭,壓頭表面光滑,壓頭 的形狀及擠壓方向決定製備的奈米碳管顧臈中奈米碳管的排列 方式。具體地,當採用平碰頭沿垂直於上述奈米碳管陣列生長 基底的方向擠壓時’可獲得奈米碳管為無序排列的各向同性的奈 米碳官碾壓膜;當採用滾概朗沿平行於基底的某-固定方向 礙壓時’可麟奈米碳㈣朗定方向取向制的奈米碳管礙壓 膜’當採用滾抽狀塵頭沿不同方向礎壓時,可獲得奈求碳管沿不 同方向取向排列的奈米碳管碾壓膜。 27 201039677 理解’虽採用上述不同方式擠屢上述的奈米碳管陣列 時由不#官會在壓力的作用下傾倒,並與相鄰的奈米碳管通過 凡仏瓦爾力相互吸引、連接形成由多個奈米碳管組成的且有自支 撑結構的奈米碳管聽膜。所述❹贿米碳管_生長基底的 表面成-央心,射,妓於等於零度且小於等於^ - 少。)。依據賴的对不同’如圖9所示,該奈米碳管礙壓膜中 的奈未碳管可沿-固定方向擇優取向排列;或如圖8所示,沿不The larger the __ structure, the smaller the thickness and the dense surface of the cyanocarbon tube. The carbon nanotubes (10) obtained from the fortune of the fortune, the carbon nanotubes = the thickness of the membrane is 1 micron to 2 mm. ❹ ' ' ' 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离 分离The pulverized structure of the tube-like structure is poured into the suction funnel through the microporous tear film: after the reduction of the lining, the Nailong carbon tube flocculation membrane is obtained. ^ The microporous membrane is - smooth surface, Kongxian (four) micron Fine. Since the gift ^ itself will provide - a larger (four) carbon nanotube floc structure, the carbon nanotube floc structure will be directly formed by suction filtration - a uniform carbon nanotube flocculation membrane. The surface of the microporous membrane is smooth. The carbon nanotube membrane is easy to be lion, and a self-supporting carbon nanotube flocculation membrane is obtained. Referring to Fig. 7, the above carbon nanotube flocculation membrane comprises intertwined. The nanocarbon & 'the carbon nanotubes are mutually attracted and entangled by van der Waals force to form a network structure, so the carbon nanotube film has good toughness. In the carbon tube flocculation membrane, the 'nano carbon tubes are uniformly distributed and irregularly arranged. It is understood that the carbon nanotubes The film has a certain thickness, and the thickness and the pressure can be controlled by the control of 26 201039677: the area and pressure of the floc structure, so the carbon nanotube film can be directly used as a nanometer. The carbon tube structure is collapsed. In addition, at least two layers of carbon nanotubes are layered or arranged side by side to form a carbon nanotube structure 164. (3) When the carbon nanotube structure 164 includes at least one nanometer The carbon tube impeding film, the preparation method of the carbon nanotube structure 164 comprises the following steps: First, a carbon nanotube is provided-formed on a growth substrate, and the array is an array of aligned carbon nanotubes. The carbon nanotube array is preferably a super-aligned carbon nanotube array. The carbon nanotube array is prepared in the same manner as the above-described carbon nanotube array. Secondly, the above-mentioned nanocarbon is squeezed by a pressure applying device. The tube array obtains a carbon nanotube rolled film, and the specific process is as follows: The pressure device applies a predetermined pressure to the above-mentioned carbon nanotubes. In the process of applying pressure, the inner tube is under pressure _ τ will be separated from the wire to form a plurality of carbon nanotubes The carbon nanotubes having a self-supporting structure impede the ruthenium film, and the 奈 one carbon carbon recording is parallel to the surface of the nano carbon embossing. In the embodiment of the invention, the pressing device is - indenter, pressure The surface of the head is smooth, the shape of the indenter and the direction of extrusion determine the arrangement of the carbon nanotubes in the prepared carbon nanotubes. Specifically, when the flat head is used to grow the substrate perpendicular to the array of carbon nanotubes. When extruded, 'the carbon nanotubes are obtained as an isotropic nano-carbon-rolled film that is disorderly aligned; when using a roll-to-roll along a certain fixed direction parallel to the substrate, it can be used. (4) The nano-carbon tube impeding film made by Langding direction orientation When the base pressure of the rolling dust head is applied in different directions, the carbon nanotube film which is aligned in different directions can be obtained. 201039677 Understand that 'the above-mentioned different ways of squeezing the above-mentioned carbon nanotube arrays are not under the pressure of the official, and they are attracted and connected with the adjacent carbon nanotubes through the van der Waals force. a plurality of carbon nanotubes and a self-supporting structure Listen carbon film tube. The surface of the abundance carbon nanotube _ growth substrate is - the center of the center, the shot, the enthalpy is equal to zero degrees and less than or equal to ^ - less. ). According to the difference of the pair, as shown in Fig. 9, the carbon nanotubes in the nano-carbon nanotubes can be arranged in a preferred orientation along the fixed direction; or as shown in Fig. 8,
同方向擇優取向湖。另,在壓力的侧下,奈米碳管陣列讀 生長的基底分離’從而使得該奈米礙管賴 從而形成-自支_奈米碳管碾_。 本技術領域技術人員翻白,上述奈米碳管_的傾倒程度 (傾角)舰力的大小有關,壓力越大,傾角越大。所述傾角為 奈米碳管陣列中的奈米碳管與生長該奈米碳管陣列的基底所呈的 夾角。製備的奈米碳管礙壓膜的厚度取決於奈米碳管陣列的高度 及壓力大小。奈米碳管陣列的高度越大而施加的壓力越小,則製 備的奈米碳管碾壓膜的厚度越大;反之,奈米碳管陣列的高度$ 小而施加的壓力越大,則製備的奈米碳管碾壓膜的厚度越小。該 奈米碳管碾壓膜的寬度與奈米碳管陣列所生長的基底的尺寸有 關,該奈米碳管碾壓膜的長度不限,可根據實際需求制得。本發 明實施例中獲得的奈米碳管碾壓膜,該奈米碳管碾壓膜的厚度為工 微米〜2毫米。 最後’將該奈米碳管碾壓膜從所述生長基底揭起,從而得到 一自支撐的奈米碳管碾壓膜。 上述奈米碳管碾壓膜中包括多個沿同一方向或擇優取向排列 28 201039677 - 的奈米碳管’所述奈米碳管之間通過凡德瓦_力相互吸引,因此 該奈米碳管膜具有很好_性。該奈米碳管礙壓膜中, 碳管均勻分佈,規則排列。 不 〃可以理解’該奈麵管碰膜具有—定的厚度,且通過奈米 碳管陣列的高纽壓力A何控概厚度。所_奈米碳管礙壓 膜可直接作為-奈米碳管結構164使用。另,可將至少兩層 碳官礙壓騎疊設置或併排設置形成—奈米碳管結構164。 ❹ # ϋ备該奈未碳管結構164包括至少—奈米碳管線狀結構 夺’違不米碳管結構164的製備方法包括以下步驟: 首先,提供至少一奈米碳管拉膜。 方法:米碳管拉膜的形成方法與㈠中奈米碳管拉膜的形成 其-人,處理該奈米碳管拉膜,形成至少一奈米碳管線。 管拉:處膜的步驟可為採用有機溶劑處理該奈米碳 〇 知用有機☆峨理該奈米碳管 劑浸騎述奈米碳管拉膜的敕銳;/料體為.將有機溶 產生的表面張力的作用有機溶劑揮發時 米碳管通過凡德瓦爾力轉;相互平行的多個奈 非扭轉而使奈米碳管拉膜收縮為一 甲醇、丙s同’、、=:、。該有機溶劑為揮發性有機溶劑,如乙醇、 ' °、一虱乙烷或氣仿,本實施例中 溶劑處理的非扭轉夺米、僧知用乙知。通過有機 膜相比,比表祕、機溶劑處理的奈米碳管拉 比細顧小’雜降低。侧解,_有機溶劑 29 201039677 虽鬲要形成非扫;轉的太乎山其令 ; 定,即不將太以=:;^讀時,奈米碳管麵的兩端不固 不設置在基絲域框架結構上。 、、知用機械外力轉該奈米好拉朗㈣為翻 所述奈米碳管糾端沿減糾 1 物蝴働狀娜=二= ΟIn the same direction, the preferred orientation lake. In addition, under the side of the pressure, the carbon nanotube array reads the growth of the substrate to separate ', thereby causing the nano-barrier to form a self-supporting nanotube. Those skilled in the art turn over, the degree of tilting (inclination) of the above-mentioned carbon nanotubes is related to the magnitude of the ship's force, and the greater the pressure, the larger the inclination. The angle of inclination is the angle between the carbon nanotubes in the array of carbon nanotubes and the substrate on which the array of carbon nanotubes is grown. The thickness of the prepared carbon nanotube barrier film depends on the height and pressure of the carbon nanotube array. The higher the height of the carbon nanotube array and the lower the applied pressure, the greater the thickness of the prepared carbon nanotube rolled film; conversely, the height of the carbon nanotube array is smaller and the applied pressure is greater. The thickness of the prepared carbon nanotube rolled film is smaller. The width of the carbon nanotube rolled film is related to the size of the substrate on which the carbon nanotube array is grown. The length of the carbon nanotube rolled film is not limited and can be obtained according to actual needs. The carbon nanotube rolled film obtained in the embodiment of the present invention has a thickness of the micron to 2 mm. Finally, the carbon nanotube rolled film is lifted from the growth substrate to obtain a self-supporting carbon nanotube rolled film. The above carbon nanotube rolled film comprises a plurality of carbon nanotubes arranged in the same direction or in a preferred orientation 28 201039677 - the carbon nanotubes are attracted to each other by van der Waals, so the nano carbon The tubular membrane is very good. In the carbon nanotube barrier film, the carbon tubes are evenly distributed and regularly arranged. It is understood that the film has a constant thickness and the thickness is controlled by the high pressure of the carbon nanotube array. The carbon nanotube film can be directly used as the carbon nanotube structure 164. Alternatively, at least two layers of carbon can be placed in a stack or arranged side by side to form a carbon nanotube structure 164. ❹# The preparation method of the carbon nanotube structure 164 including at least the nanocarbon line structure 164 includes the following steps: First, at least one carbon nanotube film is provided. Method: a method for forming a film of a carbon nanotube tube and (1) forming a film of a carbon nanotube in the middle of the film, and processing the carbon nanotube film to form at least one nano carbon line. Tube pulling: the step of filming may be to treat the nanocarbon with an organic solvent, and to use organic ☆ 峨 该 该 该 该 该 该 该 该 该 该 该 该 ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; The effect of surface tension caused by dissolution When the organic solvent is volatilized, the carbon nanotubes are rotated by van der Waals force; the mutually parallel multiple Nai non-twisting causes the carbon nanotube film to shrink to a methanol, C s with ',, =: ,. The organic solvent is a volatile organic solvent such as ethanol, '°, mono-ethane or gas-like. In the present embodiment, the solvent-treated non-twisted rice is known. Compared with the organic membrane, the nanocarbon tube is smaller than the surface treatment and the solvent treatment. Side solution, _ organic solvent 29 201039677 Although it is necessary to form a non-sweep; turn too much to the mountain; set, that is, not to read too when =:; ^, the carbon nanotubes are not fixed at both ends The base wire domain frame structure. , knowing to use the mechanical external force to turn the nano-good Lalang (four) to turn the nano carbon tube to correct the edge along the minus correction 1 material butterfly shape Na = two = Ο
成-扭轉的奈米碳管線。可以理解,上述紡紗軸的旋 轉方式不限’可正轉’也可反轉,或者正轉和反轉相結合。 進-步地’可_-揮發性有機溶继理該扭轉的夺米碳管 線。在揮發性有機溶劑揮發時產生的表面張力的作用下,處理後 的扭轉的奈米碳管線中相鄰的奈米碳管通過凡德瓦爾力=密結 合’使扭轉的奈米碳管線的比表面積減小,雜降低,與未經有 機溶劑處理的扭轉的奈米碳管線相比密度及強度均增大。、、 、再次,彻上述奈米碳管線製備至少—奈米碳管線狀結構, 並得到一奈米碳管結構164。 上述扭轉的奈米碳管線或非扭轉的奈米碳管線為一自支撐結 構,可直接作為一奈米碳管結構164使用。另,可將多個奈 管線平行排列成一束狀結構的奈米碳管線狀結構,或者將該平行 排列的多個奈米碳管線經一扭轉步驟得到一絞線結構的奈米碳管 線狀結構。進一步地,可將該多個奈米碳管線或奈米碳管線狀結 構相互平行排列、交叉排列或編織,得到一二維的奈米碳管結構 164。 30 201039677 步驟二,間隔形成一第一電 碳管_的兩端,該第4: 碳管結構164形成電連接。 ° 亥不米 所述的第一電極12及一第-你 結構偷有關。當奈米碳管^^極14的設置方式與奈米碳管 列時,如該絲碳管結至少料有序排 奈米碳官拉膜、沿一個固定 的奈米碳管撼顯者—奈米碳管 ΟA twisted nanocarbon pipeline. It will be understood that the rotation mode of the above-mentioned spinning shaft is not limited to "can be rotated" or reversed, or combined with forward rotation and reverse rotation. The step-by-step _- volatile organic solvent is followed by the twisted carbon nanotube line. The ratio of the adjacent carbon nanotubes in the treated twisted nanocarbon pipeline through the van der Waals force=tight combination to the twisted nanocarbon pipeline under the action of the surface tension generated by the volatilization of the volatile organic solvent The surface area is reduced, the impurities are reduced, and the density and strength are increased as compared with the twisted nanocarbon line which is not treated with the organic solvent. And, again, the above-mentioned nano carbon pipeline is prepared to have at least a nanocarbon line-like structure, and a carbon nanotube structure 164 is obtained. The twisted nanocarbon line or non-twisted nanocarbon line is a self-supporting structure that can be used directly as a carbon nanotube structure 164. In addition, a plurality of naphthalene pipelines may be arranged in parallel to form a bundle-structured nanocarbon line-like structure, or the parallel arrangement of a plurality of nanocarbon pipelines may be subjected to a twisting step to obtain a stranded carbon nanotube-like structure. . Further, the plurality of nanocarbon pipelines or nanocarbon pipeline structures may be arranged in parallel, crosswise or woven to each other to obtain a two-dimensional carbon nanotube structure 164. 30 201039677 Step two, the two ends of a first carbon tube _ are formed at intervals, and the fourth: carbon tube structure 164 forms an electrical connection. ° The first electrode 12 described in Haimi is related to a structure that you are stealing. When the carbon nanotubes are arranged in a manner with the carbon nanotubes, if the carbon nanotubes are at least ordered, the carbon nanotubes are pulled out along a fixed carbon nanotube. Carbon nanotube
數奈米碳管㈣—方向擇優取向排列時1 ί-第:電官結構164中的部分奈米碳管沿第—電極12 第—電極14方向延伸,使第—電極 =::r方向上。此種設置方式可保證奈二= :述的第-電極12及-第二電極14可設置在奈米碳=構 表面上或不同表面上,或者該第一電極12及一第二電 極W環繞設置於奈米碳管結構164的表面。其中,第—電極η ^一第二1:極14之間相隔設置,以使奈米碳管結構164應用於線 熱源1〇時接入—定的阻值避免短路現象產生。奈米碳管結構164 本身有报好_職與導紐,故第-電極12及-第二電極14 不'米石反督結構164之間形成很好的電接觸。 ° 所述第一電極12及一第二電極14為導電膜、金屬片或者金 ,引線該導電膜可通過電鐘、化學鍍、賤鍍、真空蒸錢、物理 氣相沈積法、化學氣相沈積法、直接塗覆或絲網印刷導電漿料或 方杨成於奈米碳管結構164表面。該金屬可為銅片或铭 片等°亥主屬片或者金屬引線可通過導電粘結劑固定於奈米碳管 31 201039677 結構164表面,或者通過翁、夾鱗駭在奈米料 發明實施例中採用真空蒸鑛法在奈米碳f結構16 ^ 細,作為第-電極12及第二電極14。 喊成兩條 所述第-電極12及-第二電極14還可為一金屬性夺 層。該奈米碳管層設置於奈米碳管結構164的表面。該夺米^ 層可通過其自身的雛或導魏結劑固定於奈米碳管結構取二 表面。該奈米石炭管層包括定向排列且均句分佈的 二 ❹ 〇 管:具體地,該奈米碳管層包括至少—奈米碳管膜歧少:= 石炭管線。優選地,所述金雜奈米碳管射 = 面包覆一金屬層,從而提高該金屬性奈米碳管層電 ^碳管射奈米碳管表面包覆金屬層的方法可為真空聽Ϊ 漿滅射或物理氣相沈積方法等。 、、 電 可以理解,在形成第_電極12及—第二電極Μ後 =兩,電引線’分別與第一電極12及第二電極 Ϊ驟:電極12及—第二電極14引出至外部電源, 步驟二,提供一基體前驢栌 輯,形成-加熱Γ:Γ 前驅體與奈米碳管結構 所述基體前㈣的材料為該基體㈣料、顿 ==材料一。該基_在-- 所述基體162的材料包括高分子材 3==:材料可包括熱塑_或熱二 物或熱固體前驅體的材料可為生成該熱塑性聚合 I、、、水口、*合物單體溶液,或該熱塑性聚合物或熱固 32 201039677 性聚合物在揮發性有機溶劑中溶解後形成的混合液。該奈米碳管 結構164直接浸泡於該液態的基體前驅體後,將該基體前驅體固 化’形成基體162與該奈米碳管結構丨科複合。The number of carbon nanotubes (4) - when the orientation is preferred, 1 ί - the partial carbon nanotubes in the electrical structure 164 extend along the first electrode 14 of the first electrode 12 so that the first electrode =::r direction . This arrangement can ensure that the first electrode 12 and the second electrode 14 can be disposed on the surface of the carbon nano surface or on different surfaces, or the first electrode 12 and the second electrode W can be surrounded. It is disposed on the surface of the carbon nanotube structure 164. Wherein, the first electrode η ^ - the second 1: pole 14 are spaced apart to allow the carbon nanotube structure 164 to be applied to the line heat source 1 接入 when the resistance value is set to avoid short circuit. The carbon nanotube structure 164 itself has a good electrical contact with the guide, so that the first electrode 12 and the second electrode 14 do not form a good electrical contact between the meter and the anti-superstructure 164. The first electrode 12 and the second electrode 14 are a conductive film, a metal piece or gold, and the conductive film can be passed through an electric clock, electroless plating, ruthenium plating, vacuum evaporation, physical vapor deposition, chemical vapor phase. The deposition process, direct coating or screen printing of the conductive paste or Fang Yang is formed on the surface of the carbon nanotube structure 164. The metal may be a copper sheet or a slab or the like. The main sheet or the metal lead may be fixed on the surface of the carbon nanotube 31 201039677 structure 164 by a conductive adhesive, or may be passed through the enamel and the ruthenium in the nanometer. In the vacuum distillation method, the nano carbon f structure is 16 μ fine as the first electrode 12 and the second electrode 14. The two said first electrode 12 and the second electrode 14 may also be a metallic layer. The carbon nanotube layer is disposed on the surface of the carbon nanotube structure 164. The layer of the rice can be fixed to the surface of the carbon nanotube structure by its own chick or a derivative. The nano-carboniferous tube layer comprises an aligned and uniformly distributed diterpenoid tube: specifically, the carbon nanotube layer comprises at least a carbon nanotube film: = carboniferous pipeline. Preferably, the gold-sandwich carbon tube emits a surface to cover a metal layer, thereby improving the surface of the metal carbon nanotube layer, and the method for coating the metal layer on the surface of the carbon nanotube tube can be vacuum Ϊ slurry shot or physical vapor deposition method. It can be understood that after forming the first electrode 12 and the second electrode = = two, the electrical lead 'is respectively connected to the first electrode 12 and the second electrode: the electrode 12 and the second electrode 14 are led to an external power source Step 2, providing a pre-matrix of the substrate, forming a heating Γ: Γ precursor and a carbon nanotube structure. The material of the front (4) of the substrate is the substrate (four) material, and the material = 1 material. The material of the substrate 162 includes a polymer material 3 ==: the material may include a thermoplastic or thermal material or a material of a hot solid precursor may be the thermoplastic polymer I, , nozzle, * a solution of the monomer solution, or a mixture of the thermoplastic polymer or thermosetting 32 201039677 polymer dissolved in a volatile organic solvent. After the carbon nanotube structure 164 is directly immersed in the liquid matrix precursor, the matrix precursor is solidified to form a matrix 162 which is combined with the carbon nanotube structure.
該無機非金屬材料可包括玻璃、陶瓷及半導體材料中的一種 或多種,故該基體前驅體可為無機非金屬材料顆粒製成的漿料、 製備該無機非金屬材料的反應氣體或呈氣態的該無機非金屬材 料。具體地,可採用真空蒸鍍、濺鍍、化學氣相沈積(CVD)及 物理氣相沈積(PVD)的方法形成氣態的基體前驅體,並使該基 體丽驅體沈積在奈米碳管結構164的奈米碳管表面。另,可將大 量無機非金屬材料顆粒在溶劑中分散,形成一漿料作為該基體前 驅體,並將該奈米碳管結構164浸泡於該漿料中,並使溶劑蒸發, 使該基體162與該奈米碳管結構164複合。 總之,當該紐前驅料液態時,歸驟三频包括將該液 態基體娜體浸醜奈来碳管結構164及@傾紐前驅體的步 驟’從而使該基體I62滲透至該奈米碳管結構164的孔隙中,形 成-加熱讀16 ;當該紐前驅體為錢時,辭驟三具體 沈積該基體前驅體於絲碳管結構164的奈米碳録蝴步=, 從而使該基體162充滿該奈米碳管結構164的孔隙中 熱元件16。 v成一加 本實施讎用注朦法將環氧樹脂基體材料與奈米 164複合,形成-加熱元件16,具體包括以下步驟:、'-。冓 步驟(-):提供-液態熱固性高分子材料。 所述液態熱固性高分子材料魄度低於5帕秒 下保持該減在3G分_上。本判魏顺軌錢== 33 201039677 液態_性高分子材料,其具體包括以下步驟: 首先’將縮水甘油_魏和縮水甘油㈣環 於一容器中,加熱至耽俄,並對容器中所述縮水甘=_環 乳和縮水甘義_氧的混合物餅料鐘,直 _環氧和縮水甘油醋型環氧的混合物混合均勾為止 其次’將猶胺和二縮水甘_加人到所频拌均勻的縮水 甘油,型祕和縮水甘油酯型環氧的混合物中進行化學反應。 ❹ 最後,將所述縮水甘_型職和縮水甘油㈣環氧的混合 =熱至30 C〜6G C ’從*得到—含環氧樹脂的賴細性高分子 驟i二):採用所述液態熱固性高分子材料浸潤所述奈米碳 官結構162。 μ本實施财_所述液態油性高分子材料浸潤所述奈米碳 管結構162的方法包括以下步驟: 首先,將奈米碳管結構162放置於一模具中。 ο 其次’將職液祕高分子㈣注射進所雜且中,读 =t==162。為了讓液態熱固性高分子材料充分浸: 所述不未%官結構162,浸潤所述奈米碳管結構162的時間不能少 於10分鐘。 社可以理解,將所述液態熱固性高分子材料浸潤所述奈米碳管 、”。構162的方法不限靖的方法,所述液祕雖高分子材料還 可^1,毛田作用被吸入到所述奈米碳管結構162中,浸潤所述奈 米碳=結構跡或者將所述奈米碳管結構脱浸泡在所述液態^ 固性高分子材料中。 …、 34 201039677 〜步驟(三):固化上述被液態熱固性高分 官結構162,得到一奈米碳管複合結構。 p卡反 括以例含環氧樹脂的_性高分子材料_化方法具體包 首先’通過-加熱裝置將該模具加熱至聊〜观,在妒产 性高分子材料為液態,維持該溫度丄小二 /、日、’使付該油性高分子材料_吸熱以增加其固化度。 ❹ 其次’繼續加熱賴具至8(rc〜觸。c,在該溫度下維持【小 時〜3小時,使得所述熱固性高分子材料繼續吸熱以增加其固化度。 再次,繼續加熱賴具至11()t〜15呢,在該溫度下維持2 小時〜2(H、時,使得所賴雕高分子㈣_贿輯加其固化 度。 最後,停止加熱,待該模具降溫至室溫後,脫模可得一奈米 碳管複合結構。 上述製備奈米碳管複合結構的具體步驟可參見范守善等人於 〇 ^07年12月26日申請的申請號為96150104的台灣專利申請。為 即省篇幅’僅引用於此,但上述申請所有技術揭露也應視為本發 明申凊技術揭露的一部分。 可以理解’上述含環氧樹脂的熱固性高分子材料的固化方法 也可採用—次升溫的方法,直接將溫度升至15CTC,使熱固性高分 子材料吸熱固化。 可以理解,上述步驟二中形成第一電極12及一第二電極14 的步驟可在形成該加熱元件16之後進行。當該基體162僅填充於 °亥示米石厌管結構164的孔隙中,從而使奈米石炭管部分暴露於加熱 35 201039677 相_法_-電極一 ΟThe inorganic non-metal material may include one or more of glass, ceramic and semiconductor materials, so the matrix precursor may be a slurry made of inorganic non-metallic material particles, a reaction gas for preparing the inorganic non-metal material, or a gaseous state. The inorganic non-metallic material. Specifically, a vacuum matrix deposition, sputtering, chemical vapor deposition (CVD), and physical vapor deposition (PVD) can be used to form a gaseous matrix precursor, and the substrate is deposited on the carbon nanotube structure. 164 carbon nanotube surface. Alternatively, a plurality of inorganic non-metallic material particles may be dispersed in a solvent to form a slurry as the matrix precursor, and the carbon nanotube structure 164 is immersed in the slurry, and the solvent is evaporated to cause the substrate 162. Combined with the carbon nanotube structure 164. In summary, when the precursor material is in a liquid state, the triaxial frequency includes a step of impregnating the liquid matrix body with the carbon nanotube structure 164 and the @倾纽 precursor, thereby allowing the substrate I62 to penetrate into the carbon nanotube. In the pores of the structure 164, a heat-reading 16 is formed; when the precursor of the precursor is money, a third carbon deposition step of the precursor of the matrix on the carbon nanotube structure 164 is specifically deposited, thereby making the substrate 162 The thermal element 16 is filled in the pores of the carbon nanotube structure 164. v In one embodiment, the epoxy resin matrix material is compounded with nano 164 by a method of injection molding to form a heating element 16, specifically comprising the following steps:, '-.冓 Step (-): Provide - liquid thermosetting polymer material. The liquid thermosetting polymer material has a twist of less than 5 Pa seconds and keeps the decrease at 3 G. This sentence Weishun rail money == 33 201039677 liquid _ polymer material, which specifically includes the following steps: First, 'glycol _ wei and glycidol (four) ring in a container, heated to 耽, and shrink in the container甘 = _ ring milk and shrinking water _ _ oxygen mixture cake clock, straight _ epoxy and glycidol vinegar type epoxy mixture mixture is hooked up next time 'willium and condensed water _ add people to the frequency mix A chemical reaction is carried out in a mixture of uniform glycidol, a secret type and a glycidyl ester type epoxy. ❹ Finally, the mixture of the glycosyl-type and glycidyl (tetra) epoxy = heat to 30 C~6G C 'from * - epoxy resin-containing fine polymer (II): using the The liquid thermosetting polymer material infiltrates the nanocarbon official structure 162. The method of infiltrating the carbon nanotube structure 162 by the liquid oily polymer material comprises the following steps: First, the carbon nanotube structure 162 is placed in a mold. ο Next, inject the liquid secret polymer (4) into the miscellaneous and read =t==162. In order to sufficiently immerse the liquid thermosetting polymer material: the non-% official structure 162, the time for infiltrating the carbon nanotube structure 162 should not be less than 10 minutes. It can be understood that the liquid thermosetting polymer material is infiltrated into the carbon nanotube, "the method of the structure 162 is not limited to the method of Jing, although the liquid material can be used as a polymer material, and the hair field effect is inhaled. Into the carbon nanotube structure 162, infiltrating the nanocarbon=structural trace or de-soaking the carbon nanotube structure in the liquid-solid polymer material. ..., 34 201039677~Step ( c) curing the above-mentioned liquid thermosetting high-segment structure 162 to obtain a carbon nanotube composite structure. The p-card is exemplified by an epoxy resin-containing _ polymer material _ method specific package first 'pass-heating device The mold is heated to chat ~ view, in the production of polymer materials is liquid, maintain the temperature 丄 small two /, day, 'to pay the oily polymer material _ heat absorption to increase its degree of cure. ❹ Second 'continue heating Lay to 8 (rc~touch.c, maintained at this temperature [hours to 3 hours, so that the thermosetting polymer material continues to absorb heat to increase its degree of solidification. Again, continue to heat the lye to 11 () t~15 At this temperature, maintain 2 hours ~ 2 (H At the time, the curing polymer (4) _ bribe is added to its degree of solidification. Finally, the heating is stopped, and after the mold is cooled to room temperature, the carbon nanotube composite structure can be obtained by demoulding. The above preparation of carbon nanotube composite For the specific steps of the structure, refer to the Taiwan Patent Application No. 96150104, which was filed on December 26, 2007 by Fan Shoushan et al. It is understood that the above-mentioned curing method of the epoxy resin-containing thermosetting polymer material can also adopt a method of raising the temperature to directly raise the temperature to 15 CTC to heat-curing the thermosetting polymer material. The step of forming the first electrode 12 and the second electrode 14 in the above step 2 may be performed after the heating element 16 is formed. When the substrate 162 is only filled in the pores of the Hemestone anatomical structure 164, thereby Part of the carboniferous tube is exposed to heat 35 201039677 phase _ method _-electrode
部包覆該奈米碳管結構二‘,進元件牛1基體162全 結構164於祕1步包括—絲職奈米碳管 14分別舰·、I牛表步驟,該第—電極12及第二電極 切宝J的牛:路的奈米碳管結構164電連接。具體地’可採用一 賴加熱元件16,以形成—切割面,從而使該奈米 二:,於加熱元件16的切割面,進而採用與步驟二相 —法將轉-電極12及—第二電極14形成於該加熱元件Μ 的切副面’從而與該暴露出來的奈米碳管結構164電連接。 可以轉’當錢米碳管結構為線糾,該第三實施例的加 熱元件36的形成方法可包括以下步驟: 首先’將絲米碳管線狀結構與所絲财驅體複合,形成 一奈米碳管線狀複合結構366 ; 其次’將-個或多個該奈米碳管線狀複合結構366排列,形 成一維的加熱元件36。 ”亥奈米奴管線狀複合結構366可相互編織、交叉、併排或盤 繞形成一二維的加熱元件36 ^當該奈米碳管線狀複合結構366相 互編織時,與織物類似地,該加熱元件36可保持一面狀。該相互 編織形成的加熱元件36可製成一加熱墊、加熱衣及加熱手套等。 當該奈米碳管線狀複合結構366相互交叉、併排或盤繞時,該多 個奈米碳管線狀結構366之間可通過粘結劑粘結,從而使該加熱 元件36保持面狀。 所述將奈米碳管線狀結構與基體前驅體複合的方式與上述步 驟三相同。 36 201039677 熱元件i表過上述步驟二的方式形成於該加 狀钍構於m、+、 可通過一切割步驟暴露該奈求碳管線 ,㈣价繼帛二電極形 _侧-電極及第二 口、厌&複口結構中的奈米碳管形成電連接。 製備Γ製備方法可進—步包括以下可選擇步驟,從而 i備具有第二貫施财的轉源20:The part encloses the carbon nanotube structure II', and enters the component cow 1 matrix 162 full structure 164 in the secret 1 step including - silk Nemi carbon tube 14 respectively, I cattle step, the first electrode 12 and The two-electrode cut Bao J's cattle: the road's carbon nanotube structure 164 is electrically connected. Specifically, a heating element 16 can be used to form a cutting surface, so that the nanometer: on the cutting surface of the heating element 16, and then the second phase method is used to turn the electrode 12 and the second An electrode 14 is formed on the tangent side of the heating element 从而 to electrically connect the exposed carbon nanotube structure 164. The method for forming the heating element 36 of the third embodiment may include the following steps: First, 'the silk-carbon carbon line-like structure is combined with the silk-rich body to form a The carbon-carbon line-like composite structure 366; nextly, one or more of the nano-carbon line-like composite structures 366 are arranged to form a one-dimensional heating element 36. The Heinerino pipeline-like composite structure 366 can be woven, crossed, side-by-side or coiled to form a two-dimensional heating element 36. When the nano-carbon line-like composite structure 366 is woven with each other, the heating element is similar to the fabric. 36. The heating element 36 formed by the mutual weaving can be made into a heating pad, a heating coat, a heating glove, etc. When the nano carbon line-like composite structures 366 cross each other, side by side or coiled, the plurality of nai The carbon-carbon line-like structures 366 can be bonded by an adhesive to maintain the heating element 36 in a planar shape. The manner of recombining the nanocarbon line-like structure with the matrix precursor is the same as that of the above step 3. 36 201039677 The heat element i is formed in the manner of the above step 2 in the addition of the structure to the m, +, and the carbonization pipeline can be exposed through a cutting step, and the (four) valence is followed by the second electrode shape _ side electrode and the second port, The carbon nanotubes in the anatomical structure are electrically connected. The preparation method can further include the following optional steps, so that the second source 20 has a conversion source 20:
Ο 步驟四,提供—支觸28,形成—熱反射層27於支撐體部 的表面。 古、土杳擇體28的表面形成一熱反射層27可通過塗覆或链膜的 、、見具體地’當該熱反射層27的材料為金属鹽或金屬氧化 可將違金屬鹽或金屬氧化物的顆粒分散於溶劑中,形成一 聚料,並將簡料錄或__於支撐體28表面,形成該熱反 射層27。根據金難或金魏化物的不同,雜辭應與金屬鹽 或金屬氧化物發生化學反應。另,該熱反射層π也可通過電錢、 化學鍍、離、真空紐、化學氣相沈積或物理氣相沈積等方^ 形成:本發明實施W細物理氣她積法在喊基板表面沈積一 層二氧化二铭層,作為熱反射層27。 步驟五,將加熱元件26設置於熱反射層27表面。 抑該加熱元件26可通過-枯結劑固定於熱反射層27表面。另, 還可採用機械g]定的方法’如制螺釘、夾板雜定裝置,將加 熱元件26四角或四邊固定於熱反射層27表面。 步驟六,形成一保濩層25於所述加熱元件26的外表面,形 成一面熱源20。 37 201039677 元件猶雜結劑或_樹峨於加熱 廟25的材料為—熱雜聚合物時, 物在高溫下卿 表面賴溢時固化形成該保護層25 一=:物,如一聚對笨,乙二_二== 如、=護層25與該加熱元件26疊加並熱壓,使保 °隻層25與加熱7L件26牢固結合。 ❹ Ο 所述的面熱源及其製備方法具有以 =構為一自支撐結構:且奈米碳管在奈丄二 步成的力^自支撐的奈米碳管結構與基體直接複合,可使複合後 Γ 件中奈米碳管仍相互結合簡—奈米碳管結構的形 而使加熱元件中奈米碳管既能均勻分佈職導電網絡,又 ==料管在溶射分散濃度的關,使奈米紗在加熱元件 =的=百分含量可達到99%,使該熱源具有更高的加熱性能。 2该基體材料的種類不限於聚合物,使該熱源的應用範圍更加 爐祕Ϊ— ’由於奈米碳管具有較好㈣度餘性,奈米碳管結 2強度較大’柔性較好,不易破裂,使其具有較長的使用壽命, 2的’纽奈轉管結構與紐基體複合形成加熱元件時,可 =構具有更廣的應用範圍。第三,奈米碳 二巾的不“&均勻4佈’因此具有均勻的厚度及電阻,發 :勻,奈米碳管的賴轉換效率高,且該奈祕f結構的單位 =熱容小於2X1G‘4焦耳每平方厘米_文,所以該面熱源具有 L速#^後小、熱響應速度快、熱交換速度快及輕射效率 门、特點。第四’奈米碳f的直徑較小,使得奈米碳管結構可具 38 201039677 可製備微型面熱源,應用於微型器件的加熱。第 過從包括奈米碳管拉膜時’該奈米碳管拉膜可通 二=二::=得到,方法簡單且有利於大面積面熱源 列,具有較好的導電二u米碳管沿同—方向擇優取向排 該奈米碳管2 _具錄㈣加無能,另, 該奈米石山有一疋透明度,可用於製備一透明熱源。第六, Ο Ο 簡單,且奈米碳^構與基體直接複合形成加熱元件的方法 人後,|& ‘、、、%件巾的含量可方便的控制。與基體複 二=:構:r=r形態,具有與純奈米碳管 一具有特定形狀的基體中料錄結射有選擇的設置於 熱,適_賴的需求。心實現局部選擇性加 利申=^述:本發明確已符合發明專利之要件,遂依法提出專 限制為本發明之佳實施例’自不能以此 之圍。舉凡習知本案技藝之人士援依本發明 圖1為本發明第一實施例的面熱源的結構示意圖。 圖2為圖1沿π_π線的剖面示意圖。 的面個岭爾嫩線狀結構 39 201039677 圖4為本發明實施例包括—彎折盤繞的奈米碳管 面熱源的結構示意圖。 線狀結構的 Ο 〇 管:熱源中的奈繼拉膜結構中奈米 鏡照片圖。6為本發明實施例面熱源中的奈米碳管拉臈結構的掃描電 電鏡=為本發明實施例面熱源中的奈米碳管絮化騎構的掃描 圖8為本發明實施例面熱源中的奈米碳管礙塵膜 碳管沿不同方向擇優取向排列的掃描電鏡照片。、、。冓中不米 圖9為本發明實施例面熱源中的 碳管沿同一方向擇優取向排列的掃描電鏡照片。構中奈 電:。為本發明實施例面熱源中的非扭轉的奈米碳管 片圖u為本發财_面_巾触制奈米碳管線的掃插電 圖12為本發明實施例面熱源中的奈米碳管拉膜 合形成的加熱元件的截斷面掃描電鏡照片。 …氣地旨複 熱源的圖論齡蝴剛__結構的面 線。圖14為使用圖12中的加熱元件在不同電愿下的溫度變化曲 發明第二實施例的面熱源的結構示意圖。 圖16為圖15沿XV_線的剖面示意圖。 石炭 米 線的婦描 鏡照片 201039677 圖17為本發明第三實施例的面熱源的結構示意圖。 圖18為本發明實施例面熱源製備方法的流程圖。 圖19為本發明實施例面熱源製備方法的奈米碳管絮狀結構的 照片。 【主要元件符號說明】Ο Step 4, providing a contact 28, forming a heat reflective layer 27 on the surface of the support body. The surface of the ancient or soil-based body 28 forms a heat-reflecting layer 27 which can pass through the coating or the chain film, see, in particular, when the material of the heat-reflecting layer 27 is a metal salt or a metal oxide, the metal salt or metal can be used. The particles of the oxide are dispersed in a solvent to form a polymer, and the material is recorded or formed on the surface of the support 28 to form the heat-reflecting layer 27. Depending on the difficulty of gold or gold, the words should chemically react with metal salts or metal oxides. In addition, the heat reflective layer π can also be formed by electricity money, electroless plating, ionization, vacuum bonding, chemical vapor deposition or physical vapor deposition, etc.: the invention implements a fine physical gas deposition method on the surface of the substrate. A layer of a second layer of dioxide is used as the heat reflecting layer 27. In step five, the heating element 26 is disposed on the surface of the heat reflective layer 27. The heating element 26 can be fixed to the surface of the heat reflecting layer 27 by a deadting agent. Alternatively, the four or four sides of the heating element 26 may be fixed to the surface of the heat reflecting layer 27 by a mechanical method such as a screw or a cleat. In step six, a protective layer 25 is formed on the outer surface of the heating element 26 to form a side heat source 20. 37 201039677 The component is still a binder or _ tree 加热 in the material of the heating temple 25 is - the thermal polymer, the material solidifies at the high temperature when the surface of the surface is cured to form the protective layer 25 =: matter, such as a pair of stupid,乙二二二== If, = the cover layer 25 is superimposed with the heating element 26 and hot pressed, so that the layer only 25 is firmly bonded to the heated 7L piece 26.面 Ο The surface heat source and the preparation method thereof have a self-supporting structure with a = structure: and the carbon nanotubes in the two-step process of the nano-tubes are directly combined with the matrix. In the composite, the carbon nanotubes are still combined with the shape of the simple carbon nanotube structure, so that the carbon nanotubes in the heating element can evenly distribute the electrical conductivity network, and the = concentration of the material dispersion in the spray dispersion. The content of the nano yarn in the heating element = 99% can be achieved, so that the heat source has higher heating performance. 2 The type of the base material is not limited to a polymer, so that the application range of the heat source is more difficult. 'Because the carbon nanotube has a good (four) degree of redundancy, the carbon nanotube junction 2 has a higher strength, and the flexibility is better. It is not easy to be broken, so that it has a long service life. When the 'Newnay tube structure and the base matrix are combined to form a heating element, the structure can be wider. Thirdly, the carbon dioxide towel does not "& uniform 4 cloth" and therefore has a uniform thickness and electrical resistance, hair: uniform, carbon nanotube conversion efficiency is high, and the unit of the structure of the mere f = heat capacity Less than 2X1G'4 joules per square centimeter, so the surface heat source has a small L speed, low heat response speed, fast heat exchange rate and light efficiency gate. The fourth 'nano carbon f diameter is smaller than that. Small, so that the carbon nanotube structure can be 38 201039677 can prepare a micro-face heat source for the heating of micro devices. When the film is covered by a carbon nanotube, the carbon nanotube film can pass two = two: := get, the method is simple and is conducive to the large-area surface heat source column, has a good conductive two-m carbon tube along the same direction, the preferred orientation of the carbon nanotube 2 _ has recorded (four) plus incompetence, another, the nano Stone Mountain has a transparency, which can be used to prepare a transparent heat source. Sixth, Ο Ο Simple, and the method of directly combining the nano carbon structure with the matrix to form a heating element, the content of |& Convenient control. With matrix complex II =: structure: r = r form, with pure carbon nanotubes The substrate with a specific shape has a selective setting in the heat, which is suitable for the demand. The heart realizes the local selective Galician = ^: The invention has indeed met the requirements of the invention patent, and the specific restrictions are imposed according to law. The present invention is directed to the preferred embodiment of the present invention. It is to be understood by those skilled in the art that the present invention is based on the present invention. FIG. 1 is a schematic structural view of a surface heat source according to a first embodiment of the present invention. FIG. 2 is a line along the π_π line of FIG. Schematic diagram of the cross section of the Lingeren linear structure 39 201039677 Figure 4 is a schematic view showing the structure of a carbon nanotube surface heat source including a bent coil according to an embodiment of the present invention. The 线 tube of the linear structure: the heat source Photomicrograph of nano mirror in the structure of the film. 6 is a scanning electron microscope of the carbon nanotube pulling structure in the surface heat source of the embodiment of the present invention = the carbon nanotube flocing structure in the surface heat source of the embodiment of the present invention Scanning FIG. 8 is a scanning electron micrograph of a carbon nanotubes in a surface heat source according to an embodiment of the present invention. The scanning electron micrographs of the carbon nanotubes in a different direction are arranged in different directions. FIG. 9 is a surface heat source according to an embodiment of the present invention. Carbon tubes are selected in the same direction Scanning electron micrograph of oriented alignment. constitutive Nylon: The non-twisted carbon nanotube sheet in the surface heat source of the embodiment of the present invention is a sweeping plug of the carbon nanotubes Fig. 12 is a cross-sectional scanning electron micrograph of a heating element formed by laminating a carbon nanotube in a surface heat source according to an embodiment of the present invention. Fig. 14 is a cross-sectional view of a structure of a regenerative heat source. FIG. 16 is a schematic cross-sectional view of the surface heat source of FIG. 15 taken along line XV_. FIG. 16 is a schematic cross-sectional view of the surface heat source of the second embodiment of the present invention. 201039677 is a schematic structural view of a surface heat source according to a third embodiment of the present invention. Fig. 18 is a flow chart showing a method for preparing a surface heat source according to an embodiment of the present invention. Figure 19 is a photograph of a carbon nanotube floc structure of a method for preparing a surface heat source according to an embodiment of the present invention. [Main component symbol description]
面熱源 10, 20, 30 第一電極 12, 22, 32 第二電極 14, 24, 34 奈米碳管片段 143 奈米碳管 145 加熱元件 16, 26, 36 基體 162, 262 奈米碳管結構 164, 264 保護層 25 熱反射層 27 支撐體 28 電極引線 29 奈米碳管線狀複合結構 366 41Surface heat source 10, 20, 30 First electrode 12, 22, 32 Second electrode 14, 24, 34 Carbon nanotube segment 143 Carbon nanotube 145 Heating element 16, 26, 36 Base 162, 262 Carbon nanotube structure 164, 264 protective layer 25 heat reflective layer 27 support body 28 electrode lead 29 nano carbon line-like composite structure 366 41
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| TWI484059B (en) * | 2012-04-28 | 2015-05-11 | Hon Hai Prec Ind Co Ltd | Method for making heating pad |
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| US1710512A (en) * | 1927-07-15 | 1929-04-23 | Anderson Pitt Corp | Heating element |
| KR100749886B1 (en) * | 2006-02-03 | 2007-08-21 | (주) 나노텍 | Heating element using carbon nanotube |
| TWI343359B (en) * | 2006-06-16 | 2011-06-11 | Hon Hai Prec Ind Co Ltd | Flexible nano electrothermal material and heating apparatus having the same |
| JP2008243774A (en) * | 2007-03-29 | 2008-10-09 | Seiko Epson Corp | Device with surface heater |
| TWI362429B (en) * | 2007-08-03 | 2012-04-21 | Hon Hai Prec Ind Co Ltd | Method of making high-density carbon nanotube array composite material |
| EP2043406B1 (en) * | 2007-09-28 | 2012-06-06 | Funate Innovation Technology Co. LTD. | Plane heat source |
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