TW201039678A - Linear heater - Google Patents

Linear heater Download PDF

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TW201039678A
TW201039678A TW98113711A TW98113711A TW201039678A TW 201039678 A TW201039678 A TW 201039678A TW 98113711 A TW98113711 A TW 98113711A TW 98113711 A TW98113711 A TW 98113711A TW 201039678 A TW201039678 A TW 201039678A
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carbon nanotube
carbon
heat source
heating element
nano
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TW98113711A
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Chinese (zh)
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TWI399121B (en
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Chang-Hong Liu
Jia-Ping Wang
Shou-Shan Fan
Kai-Li Jiang
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Hon Hai Prec Ind Co Ltd
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Abstract

The present invention relates to a linear heater. The linear heater includes a linear support, a heating element and two electrodes. The heating element is located on a surface of the linear support. The two electrodes are separately located and electrically connected to the heating element. The heating element includes at least one carbon nanotube composite structure. The carbon nanotube composite structure includes a matrix and a carbon nanotube film structure located in the matrix. The carbon nanotube film structure includes a plurality of carbon nanotubes primarily oriented along the same direction, or along two or more directions. The linear heater can be applied to different fields, such as self-heating clothes, infrared therapeutic apparatuses, electrical heaters and so on.

Description

201039678 六、發明說明: 【發明所屬之技術領域】 發明涉及-種線熱源,尤其涉及—種基於奈米碳f的線熱源。 【先前技術】 熱源在人們的生產、生活、科研情著重要的侧。線熱源 係熱源的-種,在玉業領域、科研領域或生活領域等有著廣泛的 應用,如電熱管、電熱毯、紅外治療儀及電暖器等。 Ο201039678 VI. Description of the invention: [Technical field to which the invention pertains] The invention relates to a seed line heat source, and more particularly to a line heat source based on nanocarbon f. [Prior Art] Heat sources are important aspects of people's production, life, and scientific research. Line heat source is a kind of heat source, which has a wide range of applications in the field of jade industry, scientific research or life, such as electric heating tube, electric blanket, infrared therapeutic apparatus and electric heater. Ο

先前的線熱源通常包括-線狀發熱體(如電阻絲等)及兩個電 極’該兩個電極間隔設置,並與該線狀發熱體兩端電連接。當通 過所述兩個電極向該線狀發熱體施加一電壓或通入電流時,該線 狀發熱體產生焦耳熱,且熱量以普通波長向外輕射。通常,用作 線熱源的線狀發熱體為採用金屬、合金或碳纖維製成的電熱絲。 然而,採用金屬、合金或碳纖維製成的電熱絲具有以下不足: 第一,該電熱絲所產生的熱量均以普通波長向外輻射,其電熱轉 換效率不高,不利於節省能源,需加入黏塗有遠紅外塗料的棉線 以提高電熱轉換效率。第二,碳纖維尺寸不夠小,不利於應用於 微型熱源,而金屬絲直徑很小的時候,強度很低,容易折斷,也 不利於應用於微型熱源。第三,該電熱絲的質量均較大,不利於 熱源的輕型化。另,金屬電熱絲與合金電熱絲容易被氧化,且多 次彎曲或繞折成一定角度時易產生疲勞,故,其應用受到限制。 自九十年代初以來,以奈米碳管(請參見Helical miCr〇tubules Qf graphitic carbon, Nature,Sumio Iijima,v〇i 354, p56(1991》為代表的 201039678 不米材料以其獨特的結構和性質狀人們極大的關注。近幾年 來Ik著不米故官及奈米材料研究的不斷深入,其廣闊的應用前 景不斷顯現出來。 2006年10月21日’范守善等公告的第1264754 ?虎台灣專利 中揭不種燈絲及其製備方法。該燈絲包括一奈米碳管絲。該奈 米碳管絲包括複數個通過凡德瓦爾力首尾相連的奈米碳管束,且 每個奈米碳管束包括複數個平行排列且長度基本相等的奈米破 〇管。該燈_製備方法包括如下步驟:製備奈米碳管陣列;從上 述不米厌g陣列中拉出奈米碳管絲;用均勻外力將上述步驟得到 的:米峡官絲纏繞在作為電極使用的導線上,得到燈絲。當所述 奈米碳管絲通入電流時,奈米碳管絲發出焦耳熱,並向周圍輻射 電磁波。然而,該專利文獻中的奈米碳管_於發光,由於這種 直紐得的純奈米碳管絲的機械強度與知性不夠好,使用時較容 易被破壞,從而限制奈米碳管絲的使用範圍’無法直接用於熱源。 〇 【發明内容】 、有馨於此’確有必要提供一種機械強度比較大,使用時不易 被破壞的線熱源。 一種線熱源’其包括支撐結構,—加熱 狀支撐結構的表面,及兩個雜,該_電_隨置且與該Γ 熱元件電連接,,%、+、 輔,兮心二 件包括至少—奈米碳管複合 。不;;碳讀合結構包括—基體及—奈米碳管膜結構複人 於該基體中,錢絲碳管赌魏触—岐額或不同方向 5 201039678 • 擇優取向排列的多個奈米碳管。 -種線熱源’其包括-線狀支撐結構,—加熱元件設置於線 狀支撐結構的表面,及兩個電極,該兩個電極間隔設置且與該加 熱兀件電連接’其中’所述的加熱元件包括至少一奈米碳管複合 結構,所述奈米碳管複合結構包括—奈米碳#麟構以及基體材 料,該奈米碳管膜結構包括沿i定方向或不同方姆優取向排 列的多個奈米碳管,所述基體材料複合於該奈米碳管膜結構中。 〇 —種線熱源’其包括:—線狀支撐邮;-加熱元件環繞包 覆該線狀支撐内芯,所述加熱元件包括至少一奈米碳管複合結 構,該奈米碳管複合結構包括-基體及—與之複合的奈米碳管膜 結構’且絲米碳管膜結構包括沿—固定方向或不財向擇優取 向排列的多個奈米碳管;兩個電極,該兩個電極間驗置且與該 加熱70件電連接;以及一絕緣保護層包覆該加熱元件與其内。 相較於先前技術,所述線熱源巾的加熱元件包括奈米碳管膜 〇 結構及與該奈米碳管膜結構複合的基體材料,故,該加熱元件機 械強度與韌性較大,使用時不易被破壞。 【實施方式】 以下將結合關及具體實補詳細·本發日服供的線熱源 及其製備方法。 請參閱圖1至圖3 ’本發明第-實施例提供一種線熱源2〇, 該線熱源20為一維結構。鱗熱源2G包括-線狀支撐結構 2〇2 ; -熱反射層210設置於該線狀支撐結構2〇2的表面;一加熱 6 201039678 *元^ 2G4設綱磁㈣表面;_電論間隔設置 於以加熱讀2〇4的表面,且與該加熱元件2〇4電連接;及—絕 ^護⑽設置於該加熱元件2〇4的表面。所述_源_長 度與直徑不限。優選地,所述線熱源2〇的直徑為U絲〜u厘 米。該電極206用於與外部加熱電源電連接。 所述線狀支撐結構观為一一維結構,用於支樓加熱元件 2〇4。所述線狀支撐結構观的材料可為硬性材料,如:陶究、破 〇璃、樹脂及石英等中的一種或多種,亦可選擇柔性材料,如·塑 膠及柔性纖維等中的-種或多種,用以使該線熱源2〇在使用時根 據需要料成任意形狀。優選地,所述線狀支撐結構2〇2的材料 為絕緣材料。所述線狀支撐結構2〇2的長度、餘及形狀不限, 可依據實際需要進行選擇。優選地,所述線狀支標結構2〇2的直 徑為1毫米〜i厘米。本實施例中,該線狀支樓結構2〇2為一陶究 桿,其直徑為1毫米。 〇 所述熱反射層210的材料為一對熱輻射具有較好反射效果的 絕緣材料’如:金屬氧化物、金屬鹽及陶究等中的-種或多種。 所述熱反射層21〇的厚度為動微米〜0.5毫米。本實施例中,熱 反射層210的材料優^^為三氧化二銘,其厚度為勘微米。該熱 反射層210通過濺射的方法沈積於該線狀支樓結構2〇2表面。所 述熱反射層210可用來進一步反射加熱元件2〇4所發出的熱量, 使其有效的紐到外界空間中去。該熱反射層21〇為一可選擇梦 構。 、’、’° 7 201039678 所述加熱元件204包括—奈米碳管複合結構。所述奈米碳管 複合結構包括—奈米碳管結構及基體材料。該奈㈣管結構為〆 自支撐、、σ構所’自支雜構”即該奈米碳管結構無需通過〆 支撐體支撐’也祕持自身狀的雜。該自支撐結構的奈米破 管結構包括絲齡米料,輯數贿米碳管通過凡德瓦爾力 相互吸引’從而使奈米碳f結構具有特定的做。所述奈米破管 結構中的奈米碳管包括單縣米碳管、雙縣米碳管及多壁奈米 〇碳管中的-種或多種。所述單壁奈米碳管的直徑為⑽奈米〜5〇奈 1,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 反&的直4工為I·5奈米〜5〇奈米。本發明中,該奈米碳管結構為廣 狀或線狀結構。由賊絲碳管結構具有自支雜,在不通過支 撐體支撐時仍可保持層狀或線狀結構。該奈米碳管結構中奈米破 管之間具有大量_ ’從錢該絲碳管結構具有大量微孔,所 述基體材料滲人該微孔巾,與所述奈米碳管結構緊密結合。所述 ❹奈米碳管結構的單位面積熱容小於2χ1〇-4焦耳每平方厘米開爾 文。優選地’所述奈米碳管結構的單位面積熱容可小於等於ι 7χ 10-6焦耳每平方厘米開爾文。具體地,所述奈米碳管結構可包括至 少一奈米碳管膜、至少一奈米碳管線狀結構或其組合。 所述奈米碳管複合結構可包括一層狀奈米碳管複合結構或至 少一線狀奈米碳管複合結構設置於線狀支撐結構2〇2的表面。 所述層狀奈米碳管複合結構為一二維結構。該層狀奈米碳管 複合結構可包裹或纏繞於線狀支撐結構202的表面。依據奈米碳 8 201039678 管結構與基體材料的複合方式的 的具體結構包括以下兩種情形: "層狀不未碳管複合結構 第-種情形,請參閲圖4,所述層狀其 層狀的奈米破管結構2044及―^^ 。反^设口結構包括一 乎石〜士谨遍* ^ 材料2042渗透於該層狀的奈 仏:構趣中。該魏的奈米碳管結構綱中具有大量的 微孔,5亥基體材料2042渗透於兮厚 孔中。也可理解為,此時,夺:;^盖不米碳管結構綱的微 ❹ 料 w亡仙* 構2〇44作為母體,基體材 y作為填充材峨至作為母體的奈姆結構趣内的 孔隙中。當該層狀的奈米碳管处 B#兮純加太丄 。構2〇44包括複數個奈米碳管膜 H 。結構 ϋ 树雜綠辦,_目絲雜魏結構折 心繞成-層狀自支撐結構。當該層狀的奈米碳管結構綱包 括複數個奈米碳管魏結構時,該複數個奈米碳管線狀結構可平 行雜設置、交叉設置或編織成一層狀自支撐結構。當該層狀的 不米反g、σ構2G44同時包括奈米碳管膜和奈米碳管線狀結構時, 所述奈米碳管線狀結構設置於至少一奈米碳管膜的至少一表面。 第二種情形,請參閱圖5,所述層狀奈米碳管複合結構包括一 基體2046及-奈米碳管結構綱4複合於該基體鳩中。該基體 獅為層狀結構,且該奈米碳管結構綱分佈於該基體纖中, 優選地’該奈米碳管結構綱在基體2〇46中均句分佈。該基體 2046可將該奈米碳管結㈣44 $全包覆,且該基體篇的至少 部/刀後入,亥奈米碳官結構2〇44中。當該奈求碳管結構綱為複 9 201039678 該奈米碳管線狀結 數個平行m隔設置的奈米碳管線狀結構時, 構由線狀支撐結構202的一端延伸至另一端。The prior line heat source generally includes a linear heating element (e.g., a resistance wire or the like) and two electrodes 'the two electrodes are spaced apart from each other and electrically connected to both ends of the linear heating element. When a voltage or an electric current is applied to the linear heating element through the two electrodes, the linear heating element generates Joule heat, and the heat is directly radiated outward at a normal wavelength. Usually, the linear heating element used as the line heat source is a heating wire made of metal, alloy or carbon fiber. However, the electric heating wire made of metal, alloy or carbon fiber has the following disadvantages: First, the heat generated by the electric heating wire is radiated outward at a common wavelength, and the electrothermal conversion efficiency is not high, which is not conducive to saving energy, and needs to be added to the adhesive. Cotton thread coated with far-infrared coating to improve electrothermal conversion efficiency. Second, the carbon fiber size is not small enough to be applied to a micro heat source, and when the wire diameter is small, the strength is low, it is easy to break, and it is not suitable for application to a micro heat source. Third, the quality of the heating wire is large, which is not conducive to the lightening of the heat source. In addition, the metal heating wire and the alloy heating wire are easily oxidized, and are often fatigued when bent or wound at a certain angle, so that the application thereof is limited. Since the early 1990s, the carbon nanotubes (see Helical miCr〇tubules Qf graphitic carbon, Nature, Sumio Iijima, v〇i 354, p56 (1991) for the 201039678 non-meter material with its unique structure and The nature of the people is of great concern. In recent years, Ik has been working on the research of the official and nano materials, and its broad application prospects have been continuously revealed. On October 21, 2006, Fan Shoushan and other announcements of the 1264754? Tiger Taiwan The invention discloses a filament and a preparation method thereof. The filament comprises a nano carbon tube wire, and the nano carbon tube wire comprises a plurality of carbon nanotube bundles connected end to end by van der Waals force, and each of the carbon nanotube bundles The invention comprises a plurality of nano-breaking tubes arranged in parallel and having substantially the same length. The lamp preparation method comprises the following steps: preparing a carbon nanotube array; pulling the carbon nanotubes from the above-mentioned array; using uniform The external force obtained from the above steps: the rice gorge filament is wound on the wire used as the electrode to obtain a filament. When the carbon nanotube wire is subjected to an electric current, the carbon nanotube wire emits Joule heat and is radiated to the periphery. Electromagnetic waves. However, the carbon nanotubes in this patent document _ illuminate, because the mechanical strength and the knowledge of the pure nano carbon tube wire are not good enough, it is easy to be destroyed when used, thereby limiting the carbon carbon. The scope of use of the tube wire cannot be directly used for the heat source. 〇 [Summary of the invention] It is necessary to provide a line heat source with relatively high mechanical strength and being difficult to be destroyed during use. A line heat source 'which includes a support structure , the surface of the heating support structure, and two impurities, which are electrically connected to the heat element, and the two parts of the %, +, auxiliary, and the core include at least the carbon nanotube composite. Carbon reading structure includes - matrix and - carbon nanotube membrane structure in the matrix, Qiansi carbon tube betting Wei touch - 岐 or different directions 5 201039678 • Multiple carbon nanotubes arranged in a preferred orientation - a seed line heat source 'which includes a linear support structure, a heating element disposed on a surface of the linear support structure, and two electrodes spaced apart and electrically connected to the heating element 'where' Heating element Including at least one carbon nanotube composite structure, the carbon nanotube composite structure includes a nanocarbon structure and a matrix material, and the carbon nanotube membrane structure includes an orientation along an i-direction or a different ferranistic orientation. a plurality of carbon nanotubes, the matrix material being compounded in the carbon nanotube membrane structure. The 〇-species line heat source 'includes: - a linear support post; - a heating element surrounds the linear support core, The heating element comprises at least one carbon nanotube composite structure comprising a base body and a carbon nanotube film structure composited therewith and the wire carbon nanotube film structure comprises a direction along the fixed direction or A plurality of carbon nanotubes arranged in a preferred orientation; two electrodes interposed between the two electrodes and electrically connected to the heating 70; and an insulating protective layer covering the heating element and the inside thereof. Compared with the prior art, the heating element of the wire heat source towel comprises a carbon nanotube film structure and a base material composited with the carbon nanotube film structure, so the heating element has large mechanical strength and toughness, and when used, Not easy to be destroyed. [Embodiment] Hereinafter, a line heat source and a preparation method thereof will be described in conjunction with the specific details and the daily service. Referring to FIG. 1 to FIG. 3, the first embodiment of the present invention provides a line heat source 2, which is a one-dimensional structure. The scale heat source 2G includes a linear support structure 2〇2; a heat reflective layer 210 is disposed on the surface of the linear support structure 2〇2; a heating 6 201039678 * yuan ^ 2G4 set the magnetic (four) surface; _ electrical interval setting The surface of 2〇4 is read by heating and electrically connected to the heating element 2〇4; and the protective layer (10) is disposed on the surface of the heating element 2〇4. The _source_length and diameter are not limited. Preferably, the diameter of the line heat source 2 is U wire ~ u cm. The electrode 206 is for electrical connection to an external heating source. The linear support structure is a one-dimensional structure for the branch heating element 2〇4. The material of the linear support structure may be a hard material, such as one or more of ceramics, broken glass, resin and quartz, and may also be selected from flexible materials such as plastics and flexible fibers. Or a plurality of materials for causing the line heat source 2 to be arbitrarily shaped as needed during use. Preferably, the material of the linear support structure 2〇2 is an insulating material. The length, the remainder and the shape of the linear support structure 2〇2 are not limited, and may be selected according to actual needs. Preferably, the linear branch structure 2〇2 has a diameter of 1 mm to 1 cm. In this embodiment, the linear branch structure 2〇2 is a ceramic rod having a diameter of 1 mm. The material of the heat reflecting layer 210 is a pair of insulating materials such as metal oxides, metal salts, ceramics, and the like which have a good reflection effect of heat radiation. The thickness of the heat reflecting layer 21A is a moving micrometer to 0.5 mm. In this embodiment, the material of the heat-reflecting layer 210 is preferably bismuth oxide, and the thickness thereof is micron. The heat reflective layer 210 is deposited on the surface of the linear branch structure 2〇2 by sputtering. The heat reflecting layer 210 can be used to further reflect the heat generated by the heating element 2〇4 to effectively pass it into the external space. The heat reflective layer 21 is an alternative dream. , ', '° 7 201039678 The heating element 204 comprises a carbon nanotube composite structure. The carbon nanotube composite structure comprises a carbon nanotube structure and a matrix material. The nai (four) tube structure is self-supporting, and the σ-structure is self-supporting, that is, the carbon nanotube structure does not need to be supported by the ruthenium support, and the self-supporting structure is broken. The tube structure includes the silky rice material, and the number of bribes and carbon tubes are mutually attracted by the van der Waals force, so that the nano carbon structure has a specific structure. The carbon nanotubes in the nano tube structure include a single county. One or more kinds of carbon nanotubes, double-meter carbon nanotubes, and multi-walled nano-carbon tubes. The diameter of the single-walled carbon nanotubes is (10) nm~5〇奈1, the double-walled nanometer The carbon tube has a diameter of 1 Ό nanometer to 5 〇 nanometer, and the straight wall of the multi-walled nano-anti-ampering is I·5 nm to 5 〇 nanometer. In the present invention, the carbon nanotube structure is Wide or linear structure. The carbon tube structure of the thief has self-supporting, and can maintain a layered or linear structure when not supported by the support. There are a large number of nano-tubes in the carbon nanotube structure. _ 'From the money, the carbon tube structure has a large number of micropores, and the matrix material infiltrates the microporous towel to tightly bond with the carbon nanotube structure. The heat capacity per unit area of the carbon tube structure is less than 2χ1〇-4 joules per square centimeter Kelvin. Preferably, the heat capacity per unit area of the carbon nanotube structure can be less than or equal to ι 7χ 10-6 joules per square centimeter Kelvin. The carbon nanotube structure may include at least one carbon nanotube film, at least one nano carbon line structure, or a combination thereof. The carbon nanotube composite structure may include a layered carbon nanotube composite structure or At least one linear carbon nanotube composite structure is disposed on the surface of the linear support structure 2〇2. The layered carbon nanotube composite structure is a two-dimensional structure. The layered carbon nanotube composite structure can be wrapped or wrapped The surface of the linear support structure 202. The specific structure according to the composite mode of the nanocarbon 8 201039678 tube structure and the base material includes the following two cases: " layered non-carbon tube composite structure first case, please Referring to Figure 4, the layered layered nano-tube structure 2044 and "^^". The reverse-mouth structure includes a stone-Shishen*^ material 2042 infiltrated into the layered nep: structure Interesting. The Wei's carbon nanotube structure With a large number of micropores, the 5H matrix material 2042 penetrates into the thick pores. It can also be understood that, at this time, the micro-materials of the structure of the carbon nanotubes are not destroyed. The parent body, the base material y, is used as a filler material in the pores of the Naim structure as the matrix. When the layered carbon nanotubes are B#兮 pure plus 丄, the structure 2〇44 includes a plurality of carbon nanotube membranes. H. Structure ϋ Tree arbor, _ _ _ _ Wei Wei structure folded into a layered self-supporting structure. When the layered carbon nanotube structure includes a plurality of carbon nanotubes Wei structure, the plural The nano carbon line-like structure can be arranged in parallel, cross-arranged or woven into a layer of self-supporting structure. When the layered non-g anti-g, σ-structure 2G44 includes both carbon nanotube film and nano carbon line structure The nanocarbon line-like structure is disposed on at least one surface of the at least one carbon nanotube film. In the second case, referring to Fig. 5, the layered carbon nanotube composite structure comprises a matrix 2046 and a carbon nanotube structure 4 compounded in the matrix crucible. The matrix lion is a layered structure, and the carbon nanotube structure is distributed in the matrix fiber, and preferably the carbon nanotube structure is uniformly distributed in the matrix 2〇46. The substrate 2046 can be fully coated with the carbon nanotube junction (4) 44$, and at least the portion of the substrate is inserted into the back of the substrate, and the carbon nanostructure is 2〇44. When the carbon nanotube structure is the same as the nano carbon line-like structure disposed in parallel with each other, the one end of the linear support structure 202 extends to the other end.

其二述線狀奈米碳管複合結構為―維結構。所述線狀奈米石炭 &複。結構包括兩種情形。第—種,所述線狀奈米碳管複合社構 包括一奈米碳管線狀結構及-基體材料滲透於該奈米n士 構中。該奈米碳管魏結射具妓制航,且絲材料錢 ㈣奈米碳管線狀結構的微孔t。第二種,所述線狀奈米碳管複 合結構包括-基體及至少—奈米碳管雜結構複合_基體中。 齡_6 ’當該加熱元件綱為單個線狀奈米碳管複合結構時, 該早個線狀奈米碳管複合結構可直接_於所述線狀支撐結構 =的表面。請參_ 7 ’當該加航物包括複數個線狀奈米 石厌官複合結構時,該複數個線狀奈米碳管複合結射交叉設置或 編織成-層狀結構,然後纏繞或包裹於所述線狀支擇結構2〇2表 面。 0 奈米碳管膜可包括奈米碳f拉膜、奈米碳管絮化膜或奈 米碳s賴膜。所述奈米碳管線狀結構可包括至少—解米碳管 線、複數個奈米碳管線平行排列組成的束狀結構或複數個奈米碳 官線相互扭轉組成的絞線結構。 、所述奈米碳管膜包括均勻分佈的奈米碳管,奈米碳管之間通 過凡力緊躲合。該奈米碳t膜巾的奈米碳管為無序或有 序排列。這裏的無序指奈米碳管的排列無規則,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 201039678 所述奈米碳管結構包括複數個+ :_度優選為°·5奈米,。 :應速度與其厚度有關。在相同面積的情況下,奈米二The two linear carbon nanotube composite structures are “dimensional structures”. The linear nano-carbon charcoal & The structure includes two scenarios. In the first aspect, the linear carbon nanotube composite structure comprises a nano carbon line-like structure and a matrix material is infiltrated into the nanostructure. The nano carbon tube Wei-junk 妓 妓 ,, and silk material money (four) nano carbon line-like structure of the micro-hole t. Second, the linear carbon nanotube composite structure comprises a matrix and at least a carbon nanotube heterostructure composite. Age _6 ′ When the heating element is a single linear carbon nanotube composite structure, the early linear carbon nanotube composite structure can directly be on the surface of the linear support structure. Please refer to _ 7 'When the aircraft includes a plurality of linear nano-stone composite structures, the plurality of linear carbon nanotube composites are cross-shaped or woven into a layered structure, and then wrapped or wrapped The surface of the linear structure 2〇2 is selected. The 0 carbon nanotube film may include a nano carbon film, a carbon nanotube film or a nano carbon film. The nanocarbon line-like structure may include a strand structure in which at least a carbon nanotube line, a plurality of nano carbon lines are arranged in parallel, or a plurality of nano carbon lines are twisted to each other. The carbon nanotube film comprises a uniformly distributed carbon nanotube tube, and the carbon nanotubes are separated by a force. The carbon nanotubes of the nano carbon t-film are arranged in disorder or order. The disorder here means that the arrangement of the carbon nanotubes is irregular, and the ordering here means that at least most of the arrangement of the carbon nanotubes has a certain regularity. Specifically, when the carbon nanotube structure of the carbon nanotube 201039678 includes a plurality of +: _ degrees is preferably ° · 5 nm. : The speed should be related to its thickness. In the case of the same area, nano II

二熱回應速度越慢;反之,奈料管結構的厚_ 半,Γ 。當所述奈米碳管結構的厚度為1微米〜i毫 ^不米石厌5結構在小於!秒的時間内就可達到最 度。—The second heat response speed is slower; on the contrary, the thickness of the tube structure is _ half, Γ. When the thickness of the carbon nanotube structure is 1 micron ~ i milli ^ no stone anesthesia 5 structure is less than! The maximum is achieved in seconds. -

所述奈米碳錄縣從絲碳請财直接拉取麟的—種 林自支雜的奈米碳麵。每—料碳管減包括複數個沿同 、方向擇優取向且平行於奈米碳管減表面排觸奈米碳管。所 述奈和炭管通過凡德瓦爾力首尾相連。請參閱圖8及圖9,具體 地’每-奈米碳包括複數個連續且定向排㈣奈米碳管片 段143。該複數個奈米碳管片段143通過凡德瓦爾力首尾相連。每 一奈米碳管片段143包括複數個相互平行的奈米碳管泌,該複數 _互平行的奈米碳管145通過凡德瓦爾力緊密結合。該奈米碳 官片段143具有任意的寬度、厚度、均勻性及形狀。所述奈米碳 管拉膜的厚度為G.5奈米〜麵微米,寬度與拉取該奈米碳管拉^ 的奈米碳管_的尺寸有關,長度不限。所述奈米碳錄膜及其 11 201039678 製備方法具體請參見范守善等人於2007年2月12日申嗜的,於 麵年8月16日公開的第TW2_33862號台灣公開專利申請 “奈米碳管膜結構及其製備方法”。為料,剌用於此: 但上述申請所有技術揭露也應視為本發日种請技術揭露的一部 分。當該奈米碳管結構由奈米碳妹麻成,且奈米碳管結構的 厚度比較小時’例如小於職米,該奈米碳管結構魏好的透明 度,其透光率可達爿96%,可用於冑造一透明熱源。The carbon-carbon counties in the nano-carbon counts directly draw the lining of the lining of the lining. Each carbon tube minus includes a plurality of carbon nanotubes along the same direction and direction and parallel to the surface of the carbon nanotubes. The nai and carbon pipes are connected end to end by Van der Valli. Referring to Figures 8 and 9, specifically, the per-nanocarbon includes a plurality of continuous and oriented rows of (four) carbon nanotube segments 143. The plurality of carbon nanotube segments 143 are connected end to end by Van der Waals force. Each of the carbon nanotube segments 143 includes a plurality of mutually parallel carbon nanotubes, and the plurality of mutually parallel carbon nanotubes 145 are tightly bonded by van der Waals force. The nanocarbon member segment 143 has any width, thickness, uniformity, and shape. The thickness of the carbon nanotube film is G.5 nm to face micrometer, and the width is related to the size of the carbon nanotube _ which is drawn by the carbon nanotube. For the preparation method of the nano-carbon film and its 11 201039678, please refer to the patent application "Nano Carbon" of the TW2_33862 No. TW2_33862, which was published on February 16, 2007 by Fan Shoushan et al. Tube membrane structure and preparation method thereof. In the meantime, 剌 is used for this: However, all technical disclosures of the above application should also be considered as part of the technical disclosure of this issue. When the structure of the carbon nanotube is made of nano carbon, and the thickness of the carbon nanotube structure is relatively small, for example, less than the working meter, the transparency of the carbon nanotube structure is good, and the light transmittance is up to 96%. Can be used to create a transparent heat source.

G S所述奈米碳管結構包括層迭設置的多層奈米碳管拉膜時 相鄰兩層奈米碳管拉财的擇優取向排觸奈米碳管之間形成- 交叉角度《,且α大於等於0度小於等於9〇度(化_。)。所妇 複數個奈米碳管拉膜之間或—個奈米碳管拉膜之中的相鄰的太身 碳管之間具有-定_,細在奈米碳綠射軸複數個德 孔’微孔的孔徑約小於10微米。 本發明實施_奈米碳管結構包括概伽姻方向層迭額 置的奈米碳·膜’從峨絲碳管結射的奈米碳管均沿同: 方向擇優取向排列。 所述奈米碳管碾壓膜包括均勾分佈的奈米碳管,奈米碳以 问—方向或不财向擇優取向排列。所述奈米碳管賴膜中的夺 未碳管相互料交疊,麵軌德瓦爾力她則,緊密結合, 使仔該奈米碳f闕具树好的㈣性,可彎撕姐任意形狀 而不破裂。且由於奈鱗f賴财的奈米碳管之_過凡梓瓦 爾力相互吸引’緊密結合,使奈米碳管賴膜為—自支獅結構。 12 201039678 *所述奈米碳管職膜可通過礙塵一奈米碳管陣列獲得。所述奈米 碳官礙壓财的奈米碳成奈米碳管_的生長基底的表面 形成-夾角β ’其中,P大於等於〇度且小於等於15度(〇御5。), «亥夾角β與知加在奈米碳管陣列上的壓力有關,壓力越大,該爽 角越小,優選地,該奈米碳管碾壓膜中的奈米碳管平行於該生長 基底排列。該奈米竣管健臈為通過礙壓一奈米碳管陣列獲得, 依據碾Μ的方式不同’ $奈米碳管礙壓膜巾的奈米碳管具有不同 Ο 的排卿式。具體地,請參晒10,當關-方向碾壓時,奈米 碳管沿-固定方向擇優取向排列;請參閱圖U,當沿不同方_ 壓時’奈米碳管沿獨方向擇優取向排列;當沿垂直於奈米碳管 陣列的方向賴時,奈米鮮膜各向賺。該奈料管犧壓膜中 奈米碳管的長度大於50微米。所述奈米碳管碾壓膜及其製備方法 具體請參見范守善等人於2007年6月29日申請的,於如⑽年工 月1日公開的第TW200900348號台灣專利申請“奈米碳管薄膜 〇 的製備方法。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。 該奈米碳管碾壓膜的面積和厚度不限,可根據實際需要選 擇。該奈米碳管礙壓膜的面積與奈米碳管陣列的尺寸基本相同。 该奈米碳管碾壓膜厚度與奈米碳管陣列的高度及礙壓的壓力有 關,可為1微米〜1毫米。可理解,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 米碳管陣列的高度越小而施加的壓力越大,則製備的奈米碳管碾 13 201039678 C膜的厚度越小。所述奈米碳管舰膜之巾__奈米碳管之 間具有-定間隙’從而在奈米辟賴膜中形成複數侧敬孔,微 孔的孔徑約小於10微米。The carbon nanotube structure of the GS includes a multilayered carbon nanotube film which is laminated, and a preferred orientation of the adjacent two layers of carbon nanotubes is formed between the carbon nanotubes and the carbon nanotubes - the angle of intersection ", and α It is greater than or equal to 0 degrees and less than or equal to 9 degrees (chemical _.). Between the plurality of carbon nanotube membranes or between the adjacent carbon nanotubes in the nanocarbon tube film, there is a definite _, fine in the nano carbon green axis, a plurality of de holes The pore size of the micropores is less than about 10 microns. The present invention is embodied in a nanocarbon tube structure comprising a nanocarbon film of a symmetrical gamma direction. The carbon nanotubes which are formed from the carbon nanotubes are arranged in the same orientation direction. The carbon nanotube rolled film comprises carbon nanotubes uniformly distributed, and the carbon carbon is arranged in a direction of orientation or a preferred orientation. The carbon nanotubes in the film of the carbon nanotubes overlap with each other, and the surface rail Deval force is tightly combined with the surface rails, so that the nano carbon f阙 has a good (four) nature, and can be bent and smashed. Shape without breaking. And because of the nano-carbon tubes of Nai-Feng, Lai-Gui's _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ 12 201039678 *The carbon nanotube film can be obtained by obstructing a carbon nanotube array. The surface of the growth substrate of the nanocarbon-forming carbon nanotubes of the nano-carbon is formed by an angle β′ where P is greater than or equal to 15 degrees and less than or equal to 15 degrees. The angle β is related to the pressure applied to the carbon nanotube array. The larger the pressure, the smaller the refresh angle. Preferably, the carbon nanotubes in the carbon nanotube rolled film are aligned parallel to the growth substrate. The nanotubes are obtained by obstructing a carbon nanotube array, and depending on the way of milling, the nanotubes of the nanotubes have different 排 styles. Specifically, please refer to the sun 10, when the roller is pressed in the off-direction, the carbon nanotubes are arranged along the direction of the fixed direction; see Figure U, when the pressure is different along the square, the carbon nanotubes are oriented in a single direction. Arrangement; when the film is perpendicular to the direction of the carbon nanotube array, the nano-film is earned. The length of the carbon nanotubes in the film is greater than 50 microns. For details of the carbon nanotube rolled film and the preparation method thereof, please refer to the patent application "Nano Carbon Tube" of the TW200900348 No. TW200900348, which was filed on June 29, 2007 by Fan Shoushan et al. The method for preparing the film crucible. To save space, only the above is cited, but all the technical disclosures of the above application are also considered as part of the disclosure of the technology of the present application. The area and thickness of the carbon nanotube rolled film are not limited, and may be Actually, the area of the nano-carbon tube impeding film is basically the same as that of the carbon nanotube array. The thickness of the carbon nanotube film is related to the height of the carbon nanotube array and the pressure of the pressure. It is 1 micron to 1 mm. It can be understood that 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; otherwise, the height of the carbon nanotube array The smaller the pressure exerted, the larger the thickness of the prepared carbon nanotubes 13 201039678 C film. The carbon nanotube film has a constant gap between the __nano carbon tubes Forming a plurality of side holes in the nano-diaphragm film, micro The pores have a pore size of less than about 10 microns.

所述奈米碳管結構可包減少—奈料管絮化膜,該奈米碳 管絮化膜包括相互賴且均勻分佈的奈純管。奈米碳管的長度 大於10财’優親,奈米碳管的長度大轉於測微米且小於 等於_微米。所述奈米碳管之間通過凡德瓦爾力相互吸引、纏 繞,形成網絲結構。所述奈米碳衫倾巾的奈料管為均句 分佈’無規卿列,使得該奈米碳管絮化膜各向同性。所述奈米 奴官絮化财的奈米碳管形敍量賴孔結構,微孔孔徑約小於 10微米。所述奈米碳管絮化膜的長度和寬度不限,參關, 由於在奈米碳管絮化膜中,奈米碳管相互纏緩,故,該奈米碳管 =化膜具她好的_性,码―自支撲結構,可f曲折疊成任 意形狀而不破裂。所述奈米碳管絮化賴面積及厚度均不限,厚 度為1微米1毫米,優選^⑻微米。所述奈米碳管絮化膜及其 製備方法具體請參見范守善等人於肅年5月u日中請的於 誦年11月I6日公開的第TW2·44·號台灣專利申請“奈米 碳管薄膜的製備方法”。為節省篇幅,僅引用於此,但上述申請 所有技術揭露也舰為本發明Ψ請技術揭露的_部分。 所述奈米碳管線包括複數個沿奈米碳管線_定向排列的奈 米破官。所述奈米碳管線可為非扭轉的奈米碳管線或扭轉的奈米 礙官線。該雜轉的奈米碳請為將奈米碳通過有機溶劑 201039678 -處理得到。請參閱圖l3 ’該非扭轉的奈米碳管線包括複數個沿夺 米碳管線長度方向排_奈米碳f。該扭轉的奈米碳管線為^ -機械力將所述奈米碳管拉膜兩端沿減方向扭猶得。請參閱 圖14,該扭轉的奈米碳管線包括複數個繞奈米碳管線轴向螺旋排 列的不米碳g 4非扭轉的奈米碳管線與扭轉的奈米碳管線長度 不限,直位為0.5奈米〜1〇〇微米,優選為1〇微米〜1〇〇微米。所述 奈米碳管線及其製備方法錄請參見范守料人於纖㈣月^ °曰申明的’於2_年11月21日公告的第1303239號台灣公生專 利^種奈米碳管繩及其製造方法,,,及於於2005 * 12/16 曰申明的,於2007年7月1日公開的第^^測顶伽號a灣八 開專利申請“奈米碳管絲及其製作方法,,。為節省篇幅;二 —八仁上射讀有技術揭露也應視為本發3种請技術揭露的 ‘歹地*,可採用 ,,…焊赞性有機溶劑處理該扭轉的奈米 〇線。在揮發性有機溶劑揮發時產生的表面張力的作用下,處^ 合,相鄰的奈米碳f通過凡德瓦爾力緊密結 I。a岐米碳管線的餘及比表面賴小,密度及強度增 ;4 線為採肖械频或賴力處ί!上述夺平碳 管拉膜獲得,該夺半石山乩不木反 為自支撐,。另Y縣自猶賴,故,該奈米碳管線 故該夺米Μ魅’轉米碳管射相鄰奈米碳管間存在間隙, 丁"反迷、有大量微孔,且微孔的孔徑約小於10微米。 15 201039678 所述基體觀可轉為高分子材料及無赫金屬材料等中的 -種或多種。該基體材料或職該基體材料的前驅體在—定溫度 下為液態或氣態’從而使該基赌料或絲體材料的前驅體線上 熱源20的加熱元件2〇4的製備過程中能夠渗透到該奈米碳管結構 的間隙或微孔中,與所述奈米破管結構緊密結合,固化後形成-稷合結構。該基體材料應財—定㈣熱性能,使其在該線熱源 20的工作溫度内不致破壞、變形、溶化、氣化或分解。 ❹ ’、體地’ “分子材料可包括熱塑性聚合物及熱固性聚合物 的一種或多種,如纖維素、聚對苯二曱酸乙§旨、壓克力樹脂、聚 乙稀聚丙烯、聚苯乙稀、聚氯乙烯、酚贿脂、環氧樹脂及聚 Sa等令的種或多種。該非金屬材料可包括玻璃、陶竟及半導體 材料中的種或多種。本實施例中該基體材料為環氧樹脂。該 基體材料可為柔性尚分子基底材料。該柔性高分子基底材料可選 自石夕橡膠彈性體、聚氨脂及聚甲基丙_曱酯中之-或其組合物。 〇 ㈣所料来碳官結射具有複數錄孔,祕或氣態的基 體材料或形賴紐材㈣前驅射渗人該奈米碳管結構的微孔 内部,與該奈米碳管結構緊密結合,固化後形成奈米碳管複合結 構。凊參_ 15,為沿垂直於奈米碳管拉膜中奈米碳管的排列方 =拉斷官複合結構得到的斷面照片。可發現,與環氧樹 ,複t後’該奈米碳管結構仍能基本保持複合前的形態,奈米碳 官在環氧樹脂内基本沿同一方向擇優取向排列。 所述基體材料可只填充於所述奈米碳管結構的微孔中,也可 16 201039678 進一步完全包覆整個奈米碳管結構。當該加熱元件綱包括複數 個奈米碳管結構時,該概财米碳管結财相朗隔或相 =3=基體材料中。當該奈米碳管結構為層狀結構,如為 卡二斷,奈米碳管結構可相m餘互接併排設置 二層迭处域體材料巾;t該奈米碳管結構域狀結構, Ο :米碳管線時’該線狀結構可相互間隔或相互接觸的併排設置於 f材射。#縣緣管線或絲碳管關隔設置於基體材料 時’可㈣製備該加熱元件204所需的奈米碳管結構的用量。 可視實際需要將奈米碳管職奈米碳管線設置於基體材料的 痒疋位置,從而使該加熱元件204在不同位置具有不_加熱溫 度0 可理解,所述基體材料滲透於奈米唆管結構的微孔中,可起 到固定該奈米碳管結射的奈米碳管的_,使該線熱源在使用 =財奈米碳管結射的奈米碳管不朗外力雜或刮劃而脫 :。當所述基體材料包輕個奈米碳管結構時,絲體材料可進 —步保護該奈米碳管結構,同時保證該加熱元件挪與外部絕緣。 =該基體材料可進-步起到導熱及使缝分佈均勻的目的。進 '也® u碳官結構急劇升溫時,該基體材料可起到緩衝 :、、量的作用,使該加熱元件204的溫度變化較為柔和。該基體材 ;斗還可增強整個奈米碳管複合結構的s性與勤性。 ,可理解,通過將基體材料與自支_奈米碳管結構直接複合 形成加熱元件204 ’可使奈米碳管在加熱元件2〇4中均勻分佈,且 201039678 * 奈米T的含量可為1%〜99% ’提高熱源1G的發熱溫度。由於該 不米石厌吕、、、。構為一自支樓結構,且奈米碳管在奈米碳管結構中均 勻分佈,將該自支撐的奈米碳管結構與基體材料直接複合,可使 複合後形成的加熱元件204中奈米碳管仍相互結合保持一奈米碳 官結構的形態,從而使加熱元件2〇4令奈米碳管既能均句分佈形 成導電網絡,又不受奈米碳管在溶液巾分散濃度的聞,使奈米 碳管在加熱元件中的質量百分含量可達到99%。 Ο 所述電極2G6的設置位置不限,只要與所述加熱元件204電 連接即可。所述電極206可設置於加熱元件204的同-表面上也 可設置於加熱元件204的不同表面上。所述電極2〇6可通過奈米 碳管結構的黏性或導電黏結劑(圖未示)設置於該加熱元件2⑽的 表面上。導電黏結劑在實現電極2〇6與奈米碳管結構電接觸的同 時’還可將電極206更好地固定於奈米碳管結構的表面上。具體 地,該導電黏補可為銀膠。通過該兩個電極可對加熱元件 〇 204施加電壓。其中,兩個電極206之間相隔設置,以使採用奈米 碳管結構的加熱元件204通電發熱時接入一定的阻值避免短路現 象產生。優選地,由於線狀支撐結構2〇2直徑較小,兩自電極· 間隔設置於線狀支撐結構202的兩端,並環繞設置於加熱元件2〇4 的表面。 兵體地’當該加熱元件2〇4的基體材料只填充於該奈米碳管 結構的微齡時,φ於該奈米碳管結構巾部分絲碳管的部分暴 露於該奈米碳官複合結構表面,該電極2〇6可設置於加熱元件2⑽ 18 201039678 =面上,從而使電極206與奈米碳管結構電連接。該電極施 可没置於加熱元件204的同一表面上也可設置於加熱元件綱的 上。另’當該奈米碳f複合結構的基體材料包覆整個奈 /、石反“°構時,為使該電極206與該奈来碳管結構電連接,該電 Ο ΟThe carbon nanotube structure may comprise a reduced-frozen membrane, and the carbon nanotube flocculation membrane comprises a neat tube which is mutually distributed and uniformly distributed. The length of the carbon nanotubes is greater than that of the 10's, and the length of the carbon nanotubes is greatly changed to micrometers and less than or equal to _micrometers. The carbon nanotubes are attracted and entangled by van der Waals forces to form a mesh structure. The tube of the nano-carbon shirt is a uniform distribution of the uniforms, so that the carbon nanotube film is isotropic. The nano-carbon tube shape of the nano-small granules is characterized by a pore-pore structure of less than 10 micrometers. The length and width of the carbon nanotube film are not limited, and the carbon nanotubes are mutually entangled in the carbon nanotube film, so the carbon nanotubes have a film. Good _ sex, code - self-supporting structure, can be folded into any shape without breaking. The carbon nanotubes are not limited in area and thickness, and have a thickness of 1 μm and 1 mm, preferably ^ (8) μm. For the specific description of the carbon nanotube film and the preparation method thereof, please refer to the TW2·44. Taiwan patent application "Nemi" published by Fan Shoushan and others in the May 1st of the year. Preparation method of carbon tube film". In order to save space, only the above is cited, but all the technical disclosures of the above application are also part of the invention disclosed in the technical disclosure. The nanocarbon pipeline includes a plurality of nano-organisms arranged along a nanocarbon line. The nanocarbon line can be a non-twisted nanocarbon line or a twisted nano-barrier line. The miscible nanocarbon is obtained by treating nanocarbon with organic solvent 201039678 -. Please refer to Figure l3'. The non-twisted nanocarbon pipeline includes a plurality of rows of carbon nanotubes along the length of the carbon nanotubes. The twisted nano carbon line is mechanically forced to twist both ends of the carbon nanotube film in a decreasing direction. Referring to FIG. 14, the twisted nanocarbon pipeline includes a plurality of non-twisted nano carbon pipelines arranged in an axial spiral arrangement around the carbon nanotubes, and the length of the twisted nanocarbon pipeline is not limited. It is from 0.5 nm to 1 μm, preferably from 1 μm to 1 μm. The nano carbon pipeline and its preparation method are recorded in the sample of Fan Shouzhong Yufu (four) month ^ ° 曰 的 ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' ' Rope and its manufacturing method, and, as stated in the 2005 * 12/16 曰, the first patent application "Nan carbon nanotube wire and its production" published on July 1, 2007 Method, in order to save space; the second-eighths on the reading of the technical disclosure should also be regarded as the three types of this technology, please disclose the '歹地*, can be used, ..., the welding of organic solvents to treat the twisted Nai Rice bran line. Under the action of the surface tension generated by the volatilization of volatile organic solvents, the adjacent nano-carbon f is tightly bound by the van der Waals force. Small, density and strength increase; 4 lines for the acquisition of mechanical frequency or Lai Li ί! The above flattened carbon tube film obtained, the half-stone mountain is not self-supporting. The nano carbon pipeline should be the same as the gap between the carbon nanotubes and the adjacent carbon nanotubes, and there is a large amount of micropores. The pore size of the pores is less than about 10 μm. 15 201039678 The substrate body can be converted into one or more kinds of polymer materials and non-metal materials, etc. The matrix material or the precursor of the matrix material is at a constant temperature. a liquid or gaseous state such that the precursor of the heating element 2〇4 of the heat source 20 on the precursor line of the base or filament material can penetrate into the gap or micropores of the carbon nanotube structure, The structure of the broken pipe is tightly combined and forms a composite structure after solidification. The base material should have a thermal property of (4), so that it does not damage, deform, dissolve, vaporize or decompose within the working temperature of the heat source 20 of the wire. ', body' 'Molecular materials may include one or more of thermoplastic polymers and thermosetting polymers, such as cellulose, poly(p-benzoic acid), acrylic resin, polyethylene polypropylene, polystyrene Species or types of rare, polyvinyl chloride, phenolic brittle, epoxy resin, and poly-Sa. The non-metallic material may include one or more of glass, ceramics, and semiconductor materials. In this embodiment, the base material is an epoxy resin. The matrix material can be a flexible molecular substrate material. The flexible polymeric substrate material can be selected from the group consisting of Shishi rubber elastomer, polyurethane and polymethyl propyl acrylate - or a combination thereof. 〇 (4) It is expected that the carbon official jet has a plurality of recorded pores, a secret or gaseous matrix material or a shaped material (4). The precursor is infiltrated into the microporous structure of the carbon nanotube structure, and is closely integrated with the carbon nanotube structure. After curing, a carbon nanotube composite structure is formed. The ginseng _ 15, is a cross-sectional photograph of the arrangement of the carbon nanotubes in the film perpendicular to the carbon nanotubes. It can be found that, with the epoxy tree, after the complex t, the carbon nanotube structure can still maintain the shape before the composite, and the nanocarbon is arranged in the same direction in the epoxy resin. The base material may be filled only in the micropores of the carbon nanotube structure, or may further completely coat the entire carbon nanotube structure at 16 201039678. When the heating element comprises a plurality of carbon nanotube structures, the carbon nanotubes are marginally separated or phase = 3 = in the matrix material. When the structure of the carbon nanotube is a layered structure, if the card is broken, the carbon nanotube structure can be arranged in parallel with each other to form a two-layered domain material towel; t the carbon nanotube domain structure , Ο : When the rice carbon line is used, the linear structures may be arranged side by side or in contact with each other to be placed on the f-material. When the county line or the carbon tube is disposed at the base material, the amount of the carbon nanotube structure required for the heating element 204 can be prepared. It can be understood that the carbon nanotube Nike carbon pipeline can be disposed at the itch position of the base material according to actual needs, so that the heating element 204 has a non-heating temperature 0 at different positions, and the matrix material penetrates into the nano tube. The micropores of the structure can be used to fix the carbon nanotubes of the carbon nanotubes, so that the heat source of the line is not used or scraped by the carbon nanotubes which are formed by using the carbon nanotubes. Take it off: When the base material is light in a carbon nanotube structure, the filament material can further protect the carbon nanotube structure while ensuring that the heating element is insulated from the outside. = The base material can be used for further heat conduction and uniform distribution of the seam. When the 'Ultra® u carbon official structure is heated rapidly, the base material acts as a buffer to reduce the temperature of the heating element 204. The base material can also enhance the sity and diligence of the entire carbon nanotube composite structure. It can be understood that the carbon nanotubes can be evenly distributed in the heating element 2〇4 by directly combining the base material with the self-supporting carbon nanotube structure to form the heating element 204', and the content of 201039678*nano T can be 1% to 99% 'Improve the heat generation temperature of the heat source 1G. Because of the non-meter stone, Lu,,,. The structure is a self-supporting structure, and the carbon nanotubes are uniformly distributed in the carbon nanotube structure, and the self-supporting carbon nanotube structure is directly combined with the matrix material, so that the heating element 204 formed in the composite can be The carbon nanotubes are still combined with each other to maintain the shape of a nanometer carbon structure, so that the heating element 2〇4 allows the carbon nanotubes to be distributed evenly to form a conductive network, and is not affected by the concentration of the carbon nanotubes in the solution towel. The mass percentage of the carbon nanotubes in the heating element can reach 99%. The arrangement position of the electrode 2G6 is not limited as long as it is electrically connected to the heating element 204. The electrodes 206 may be disposed on the same surface of the heating element 204 or on different surfaces of the heating element 204. The electrode 2〇6 may be disposed on the surface of the heating element 2 (10) through a viscous or conductive adhesive (not shown) of a carbon nanotube structure. The conductive bonding agent can also better secure the electrode 206 to the surface of the carbon nanotube structure while achieving electrical contact between the electrode 2〇6 and the carbon nanotube structure. Specifically, the conductive adhesive may be silver paste. A voltage can be applied to the heating element 〇 204 through the two electrodes. Wherein, the two electrodes 206 are spaced apart to allow a certain resistance value to be avoided when the heating element 204 using the carbon nanotube structure is energized to prevent short circuit. Preferably, since the linear support structure 2〇2 has a small diameter, the two self-electrodes are spaced apart from both ends of the linear support structure 202 and surround the surface of the heating element 2〇4. When the base material of the heating element 2〇4 is only filled in the micro-age of the carbon nanotube structure, φ is partially exposed to the carbon carbon tube in the portion of the carbon nanotube structure. The composite structure surface, the electrode 2〇6 may be disposed on the heating element 2(10) 18 201039678=face, thereby electrically connecting the electrode 206 to the carbon nanotube structure. The electrode application may not be placed on the same surface of the heating element 204 or may be disposed on the heating element. Further, when the base material of the nanocarbon f composite structure covers the entire nano/rock structure, in order to electrically connect the electrode 206 to the carbon nanotube structure, the electric Ο

:1 2°6可物谢,細碳管結構接 。此時’為使該電極206與外部電源導通,該電極挪可部分 暴露於奈米碳管複合結構之外;或者,雜鱗2G可進—步Z 兩條引線’分顺麵個馳料接,並㈣奈米碳管複合 結構内部引出。 σ 奈米碳管結構中的奈米碳管有序排列時,優選地該奈 米碳官的排列方向沿從—個電極206至另一電極挪方向延伸。 具體地’當該奈米碳管結構包括至少—奈米碳管拉膜時,所述兩 ^電極206分別設置於該奈米碳管拉膜的兩端,使奈米碳管拉膜 ^奈未碳官從-個電極寫至另一電極2㈤的方向首尾相連定 向排列。 所述電極2〇6為導電薄膜、金屬片或者金屬化線。該導電薄 2的材料可為麵、合金、銦聽化物(1則、錄魏化物(細)、 2膠、導電聚合轉。該導電_可通過物理氣相沈積法、 2乳相沈積法或其他方法形成於加熱元件204表面。該金屬片 屬⑽的材料可為則侧等。該金屬片可通過導電黏 Ισ劑固定於加熱元件204表面。 所述電極206运可為—奈米碳管結構。該奈米碳管結構可通 19 201039678 過其自身的黏性或導電黏結劑固^於熱反射層21()或線狀支撐結 構202的表面。該奈米碳管結構包括定向排列且均勾分佈的金屬 性奈米碳管。具體地,該奈米碳f結構包括至少—絲碳管拉膜 或至少一奈米碳管線。 本實施例t ’優·,將兩個奈米碳管_分職置於沿線 狀支撐結構202長度方向的兩端作為電極2〇6。該兩個奈米碳管拉 膜環繞於加熱元件2〇4 _絲,並通料餘結織加熱元件 〇 204之間形成電接觸。所述導電黏結劑優選為轉。由於本實施例 中的加熱元件204也採用奈米碳管結構,故,電極2〇6與加熱元 件2〇4之間具有較小的歐姆接觸電阻,可提高線熱源、對電能的 利用率。 可理解’電極206的結構和材料均不限,只要能向所述奈米 壤管複合結構中輸人電流的方式都在本發明的保護範圍内。: 1 2 °6 can be thank you, the thin carbon tube structure is connected. At this time, in order to make the electrode 206 be connected to the external power source, the electrode may be partially exposed to the carbon nanotube composite structure; or, the weft scale 2G may be advanced to the step Z, and the two leads are separated by a smooth surface. And (4) the internal structure of the carbon nanotube composite structure. When the carbon nanotubes in the σ-nanocarbon nanotube structure are arranged in an order, it is preferable that the alignment direction of the carbon nanotubes extends in the direction from the one electrode 206 to the other electrode. Specifically, when the carbon nanotube structure includes at least a carbon nanotube film, the two electrodes 206 are respectively disposed at both ends of the carbon nanotube film, so that the carbon nanotube film is not coated. The carbon officer is oriented from the end of one electrode to the other electrode 2 (five). The electrode 2〇6 is a conductive film, a metal piece or a metallized wire. The material of the conductive thin 2 can be a surface, an alloy, an indium listener (1, a film of fine (fine), 2 glue, conductive polymerization. The conductive_ can be by physical vapor deposition, 2 emulsion deposition or Other methods are formed on the surface of the heating element 204. The material of the metal sheet (10) may be a side, etc. The metal sheet may be fixed to the surface of the heating element 204 by a conductive adhesive σ agent. The electrode 206 may be a carbon nanotube The carbon nanotube structure can be bonded to the surface of the heat-reflecting layer 21 () or the linear support structure 202 by its own viscous or conductive adhesive through 19 201039678. The carbon nanotube structure includes orientation and The metal carbon nanotubes are uniformly distributed. Specifically, the nano carbon f structure includes at least a carbon nanotube film or at least one nano carbon line. In this embodiment, t 'you·, two nano carbons The tube_partition is placed at both ends along the length direction of the linear support structure 202 as the electrode 2〇6. The two carbon nanotube film is wound around the heating element 2〇4 _ wire, and the remaining woven heating element 〇 Electrical contact is formed between 204. The conductive adhesive is preferably a turn. The heating element 204 in the embodiment also adopts a carbon nanotube structure, so that the electrode 2〇6 and the heating element 2〇4 have a small ohmic contact resistance, which can improve the utilization of the line heat source and the electric energy. The structure and material of the electrode 206 are not limited, as long as the current can be input to the nano-tube composite structure within the protection scope of the present invention.

所述絕緣保護層208的材料為一絕緣材料,如:橡膠及樹脂 〇等中的—種或多種。所述絕緣保護層厚度不限,可根據實際 情況選擇。所述絕緣保護層208的厚度為0.5毫米〜2毫米。本實 施例中’該絕緣保護層的材料採用橡膠,其厚度為Μ毫米。 所述絕=保護層208用來防止該線熱源2〇使用時與外界形成電接 觸’同#還可防止加熱層204中的奈米碳管結構吸附外界雜質。 <理解,該絕緣保護層208為-可選擇結構Q j米碳管具有良好的導電性能及熱穩定性,且作為—理想的 黑體。構具有比車父局的熱輻射效率。將本實施例的線熱源的 20 201039678 兩個電極206連接導線後接入電源,施加一定電壓於所述奈米碳 管複合結構,線熱源20中的奈米碳管複合結構即可輻射出一定波 長範圍的電磁波。當奈米碳管結構的面積大小一定時,通過調節 電源電壓大小和奈米碳管結構的厚度,該線熱源2〇可輻射出不同 波長範圍的電磁波。電源電壓的大小一定時,奈米碳管結構的厚 度和線熱源20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,奈米碳管結構的厚度越厚,線熱源20輻射出電磁 波的波長越短;奈米碳管結構的厚度越薄,線熱源2〇輻射出電磁 波的波長越長。具體地’該奈米碳管結構可產生一紅外線熱輻射。 奈米碳管結_厚度-定時,·輕社小和賴源2()輕射出 的電磁波的波長成反比。即當奈米碳管結構的厚度一定時,電源 電壓越大’線熱源2〇輻射出的電磁$皮的波長越短;電源電壓越小, 線熱源20輻射出的電磁波的波長越長。 可理解,該線熱源20於應用時應根據基體材料_熱性限制 施加於兩個電極2〇6兩端的㈣大小,使奈米碳管複合結構的發 熱溫度控制於該基體材料能耐受的溫度範圍内。例如,當該基體 材料為有機高分子聚合物時,該電壓小於等於1〇伏,該熱源的發 熱溫度為赋以下。當該基體材料為陶竟時,該電壓範圍為犯 伏〜30伏,該熱源的發熱溫度可為12(rc〜5〇〇<^。 當該線熱源20的奈米碳管複合結構中的基體材料為柔性的聚 合物材料’且線狀支撐結構202也由柔性材料製作時,該線妖源 20為-柔性線熱源20。該線熱源2〇使用時,可將其設置於所要 201039678 力‘、’、的物體表面或將其與被加熱的㈣間隔設置,彻其 即他亍加熱。另,__躲熱__編織成= 預疋的圖形使用。該柔性的線熱源2〇可用於製造自發 服、取暖手套絲錄、電加熱器、紅外治療儀、麵器等= 有廣泛的應用範圍。 一 請參閱圖16,本發明第一實施例進—步提供上述線熱源2〇的 製備方法,其具體包括以下步驟: 、 〇 步驟S101,提供一奈米碳管結構。 根據奈米碳管結構料同’所述奈米碳管結構的製備方法包 ^直接拉麟、碾驗、絮化法等。下婦對上料種奈米^ 官結構的製備方法進行分別敍述。 (一)當該奈米碳管結構包括至少一奈米碳管拉膜,該奈米 石反管結構的製備方法包括以下步驟: 首先,提供-奈米碳管陣列形成於一生長基底,該陣列優選 〇 為超順排的奈米碳管陣列。 該奈米碳管陣列的製備方法採用化學氣相沈積法,其具體步 驟包括.(a)提供一平整生長基底,該生長基底可選用p型或N 型石夕生長基底’或選用形成有氧化層时生長基底,本發明實施 例優選為採用4英寸的石夕生長基底;⑻於生長基底表面均句形 成一催化劑層,該催化劑層材料可選用鐵(Fe)、鈷(c〇)、鎳(Ni) 或其任意組合的合金之一;(c)將上述形成有催化劑層的生長基 底於700°C〜90(TC的空氣中退火約30分鐘~90分鐘;(d)將處理 22 201039678 過的生長基底置於反應爐中,並於保護氣體環境下加熱到5〇〇。〇 〜740 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。該奈米碳管陣列為複數個彼此平行且垂直於生長基底 生長的奈米碳管形成的純奈米碳管陣列。通過上述控制生長條 件,該定向排列的奈米碳管_中基本不含有雜質,如無定型碳 或殘留的催化劑金屬顆粒等。 本發明實齡j提供的奈米碳管_,丨為單壁奈米碳管陣列、雙 〇 壁奈米碳管_及錄奈米碳管_中的—種。所述奈米碳管的 直徑為1奈米〜50奈米,長度為5〇奈米〜5毫米。本實施例十,奈 米碳管的長度優選為100微米〜900微米。 本發明實施例t碳賴可乙快、乙埽、甲鮮化學性質 較活潑的碳氩化合物,本發明實施例優選的碳源氣為乙块;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氮氣。 可理解,本發明實施例提供的奈米碳管陣财限於上述製備 〇 方法’也可為石墨電極恒流電孤放電沈積法、雷射蒸發沈積法等。 其次’採用-拉伸工具從奈米碳管陣列中拉取奈米碳管獲得 至少:米碳管拉膜,其具體包括以下步驟:(a)從所述超順排 不米喊官陣財選定—個或具有—定寬度的複數個奈米碳管,本 f施例優選為採用具有一定寬度的膠帶、鱗子或夹子接觸奈米碳 管陣列以敎-個或具有m的複數個奈米碳管;⑻以一 定速度拉伸錢定的奈米碳管,從而形成首尾相連的複數個奈米 碳管片段,進而形成一連續的奈米礙管膜。該拉取方向沿基本垂 23 201039678 直於奈米碳管陣列的生長方向。 上述拉伸過財’該減個奈米碳管片段練力作用下沿拉 伸方向逐漸生長基底_時,由於凡德㈣力_,該選定 的複數個奈米碳管片段分別與其他奈米碳管片段首尾相連地連續 地被拉出,從⑽成-連續、均勻且具有—定寬度的奈米礙管膜。 該奈米碳麵包括減㈣尾械的奈米碳管,縣米碳管基本 沿拉伸方向綱。請參_ 8及圖9 ’該絲碳麵包括複數轉The material of the insulating protective layer 208 is an insulating material such as rubber or resin enamel or the like. The thickness of the insulating protective layer is not limited and may be selected according to actual conditions. The insulating protective layer 208 has a thickness of 0.5 mm to 2 mm. In the present embodiment, the material of the insulating protective layer is rubber, and its thickness is Μ mm. The absolute protective layer 208 is used to prevent the line heat source 2 from forming an electrical contact with the outside when it is used. The same can prevent the carbon nanotube structure in the heating layer 204 from adsorbing foreign impurities. <Understanding that the insulating protective layer 208 is an optional structure Q j m carbon tube has good electrical conductivity and thermal stability, and serves as an ideal black body. The structure has a heat radiation efficiency higher than that of the parent's office. The two electrodes 206 of the line heat source 20 201039678 of the present embodiment are connected to the power supply, and a certain voltage is applied to the carbon nanotube composite structure, and the carbon nanotube composite structure in the line heat source 20 can radiate a certain amount. Electromagnetic waves in the wavelength range. When the area of the carbon nanotube structure is constant, the line heat source 2 辐射 can radiate electromagnetic waves of different wavelength ranges by adjusting the power supply voltage and the thickness of the carbon nanotube structure. When the magnitude of the power supply voltage is constant, the thickness of the carbon nanotube structure and the wavelength of the electromagnetic wave radiated by the line heat source 20 are opposite. That is, when the power supply voltage is constant, the thicker the thickness of the carbon nanotube structure, the shorter the wavelength of the electromagnetic wave radiated by the line heat source 20; the thinner the thickness of the carbon nanotube structure, the longer the wavelength of the electromagnetic wave emitted by the line heat source 2〇 . Specifically, the carbon nanotube structure produces an infrared heat radiation. The carbon nanotube junction _ thickness - timing, · light social small and Lai source 2 () lightly emitted electromagnetic wave wavelength is inversely proportional. That is, when the thickness of the carbon nanotube structure is constant, the power supply voltage is larger. The shorter the wavelength of the electromagnetic light radiated by the line heat source 2 is, the smaller the power supply voltage is, and the longer the wavelength of the electromagnetic wave radiated by the line heat source 20 is. It can be understood that the line heat source 20 should be applied to the (four) size of the two electrodes 2〇6 according to the heat limit of the base material, so that the heating temperature of the carbon nanotube composite structure is controlled to a temperature that the base material can withstand. Within the scope. For example, when the base material is an organic high molecular polymer, the voltage is 1 volt or less, and the heat generation temperature of the heat source is below. When the base material is ceramic, the voltage range is 〜30 volts, and the heat generation temperature of the heat source may be 12 (rc~5〇〇<^. When the line heat source 20 is in the carbon nanotube composite structure When the base material is a flexible polymer material' and the linear support structure 202 is also made of a flexible material, the line source 20 is a flexible line heat source 20. When the line heat source 2 is used, it can be set at the desired 201039678. The surface of the object of force ', ', or it is placed at a distance from the heated (four), and then it is heated by others. In addition, __hidden heat __ weaving into = pre-turned pattern use. The flexible line heat source 2〇 It can be used in the manufacture of spontaneous clothing, heating gloves, electric heaters, infrared therapeutic devices, facial devices, etc. = has a wide range of applications. Referring to Figure 16, the first embodiment of the present invention provides the above-mentioned line heat source 2〇. The preparation method comprises the following steps: 〇 Step S101, providing a carbon nanotube structure. According to the preparation method of the carbon nanotube structure material and the carbon nanotube structure, the method directly comprises , flocculating method, etc. The preparation method is separately described. (1) When the carbon nanotube structure comprises at least one carbon nanotube film, the preparation method of the nano stone back tube structure comprises the following steps: First, providing a carbon nanotube array formation In a growth substrate, the array is preferably a super-aligned carbon nanotube array. The carbon nanotube array is prepared by chemical vapor deposition, and the specific steps include: (a) providing a flat growth substrate, The growth substrate may be selected from a p-type or N-type growth substrate or a growth substrate formed by forming an oxide layer, and the embodiment of the present invention preferably uses a 4 inch growth substrate; (8) a catalyst is formed on the surface of the growth substrate. a layer, the catalyst layer material may be selected from one of iron (Fe), cobalt (c), nickel (Ni) or any combination thereof; (c) the growth substrate formed with the catalyst layer described above at 700 ° C ~ 90 (The air in TC is annealed for about 30 minutes to 90 minutes; (d) The growth substrate of process 22 201039678 is placed in a reaction furnace and heated to 5 Torr under a protective gas atmosphere. 〇~740 C, then pass Carbon source gas reaction 5 minutes to 3 minutes, growth to obtain a carbon nanotube array. The carbon nanotube array is a plurality of pure carbon nanotube arrays formed by carbon nanotubes which are parallel to each other and grow perpendicular to the growth substrate. The condition that the aligned carbon nanotubes contain substantially no impurities, such as amorphous carbon or residual catalyst metal particles, etc. The carbon nanotubes provided by the present invention are 单, and the 丨 is a single-walled carbon nanotube. The array, the double-walled carbon nanotubes, and the nanocarbon tube _. The carbon nanotubes have a diameter of 1 nm to 50 nm and a length of 5 〇 nanometers to 5 mm. In the tenth embodiment, the length of the carbon nanotubes is preferably from 100 micrometers to 900 micrometers. In the embodiment of the invention, the carbon argon compound having a relatively high chemical activity, such as carbon argon, acetophenone, and methyl fresh, is preferred in the embodiment of the present invention. The source gas is a block; the shielding gas is nitrogen or an inert gas, and the preferred shielding gas in the embodiment of the invention is nitrogen. It can be understood that the carbon nanotube array provided by the embodiment of the present invention is limited to the above-mentioned preparation method ’, and may also be a graphite electrode constant current electric soli discharge deposition method, a laser evaporation deposition method, or the like. Secondly, the 'stretching tool is used to pull the carbon nanotubes from the carbon nanotube array to obtain at least: the carbon nanotube film, which specifically includes the following steps: (a) from the super-shun Selecting a plurality of carbon nanotubes having a constant width, the present embodiment preferably uses a tape having a certain width, a scale or a clip to contact the array of carbon nanotubes to have a plurality of n or a plurality of n The carbon nanotubes are (8) stretching the carbon nanotubes at a certain speed to form a plurality of carbon nanotube segments connected end to end, thereby forming a continuous nano-membrane film. The pulling direction is perpendicular to the growth direction of the carbon nanotube array along the basic vertical 23 201039678. The above-mentioned stretching has been carried out under the action of reducing the carbon nanotube fragments to gradually grow the substrate along the stretching direction, due to the van der (four) force _, the selected plurality of carbon nanotube segments respectively and other nanoparticles The carbon tube segments are continuously pulled out end to end, from (10) to a continuous, uniform, and narrow width of the nanotube film. The carbon surface of the nanometer includes a carbon nanotube of minus (four) tailings, and the carbon nanotubes of the county are basically along the direction of stretching. Please refer to _ 8 and Figure 9 'The carbon surface of the wire includes multiple turns

優取向排列的奈米碳管心進一步地,所述奈米碳管膜包括複數 個首尾树且定向祕米碳”段M3,奈米碳管諸⑷ 兩端通過凡德瓦爾力相互連接。該奈米碳管片段143包括複數個 被平行排觸絲碳管145。該直絲傾得奈米碳管膜的方法 簡單快速’適宜進行工業化應用。 μ該奈米碳麵的寬度絲树管_的尺寸相,該奈米碳 、的長度不限,可根據實際需求娜。當該絲碳管陣列的面 積為4英寸時,該奈米碳管膜的寬度為Q 5奈㈣厘米該奈米 碳管膜的厚度為0.5奈米〜100微米。 最後上述奈米碳管拉_備絲碳管結構。 〜該奈米絲_可直接作為—絲碳管結構使用。進-步, 個奈米碳管拉膜平行無_或/和重_設得到—奈 :::。由於該奈米碳管拉膜具有較大的比表面積,故,該 ί’㈣|蝴_目互緊密結合 觸結構。蝴細射,奈赠拉膜的層數 24 201039678 奈米碳管拉一 —_9〇具體可依據實際需求製備。 本實施例中,進—步包括用有機 驟,該有機溶劑為揮發性有機、、1丨处不未心、、、。構的步 二氣乙院和氣仿中一種或::::選=醇”、 有機溶劑處理的步驟具體為:將該奈嫌結Preferably, the carbon nanotube film comprises a plurality of head-to-tail trees and oriented Mimi carbon "section M3, and both ends of the carbon nanotubes (4) are connected to each other by van der Waals force. The carbon nanotube segment 143 comprises a plurality of parallel-contacted carbon nanotubes 145. The method of straightening the carbon nanotube film is simple and rapid 'suitable for industrial application. μ The width of the nano-carbon surface of the silk tree tube _ The size of the nanocarbon, the length of the nanocarbon, is not limited, according to the actual demand. When the area of the carbon nanotube array is 4 inches, the width of the carbon nanotube film is Q 5 na (four) cm. The thickness of the carbon tube film is 0.5 nm to 100 μm. Finally, the above-mentioned carbon nanotubes are pulled _ the silk carbon tube structure. ~ The nanowire _ can be directly used as a carbon tube structure. Step-by-step, one nanometer The carbon tube is not parallel to the _ or / and the weight _ is obtained - Nai::: Since the carbon nanotube film has a large specific surface area, the ί' (4) | Butterfly fine shot, the number of layers of the film is released 24 201039678 Nano carbon tube pull one - _9 〇 can be based on actual demand In this embodiment, the step further comprises: using an organic solvent, the organic solvent is volatile organic, and the organic solvent is not unintentional, and the structure is one of the two types of gas and gas: or:::: = alcohol", the organic solvent treatment step is specifically: the nasty

π太f 轉結構上,通過鮮將有機溶劑滴落 == 瓣輪碳陶,❹,也可將上述 社構汉入盛有有機溶劑的容器中浸潤。所述的奈米碳管 ▲有機溶劑浸潤處理後’當奈米碳管膜的層數較少時,於表 作用下’奈米碳管膜中相鄰的奈米碳管會收縮成間隔分 佈的不米碳管線。而當奈米碳管膜的層數較多時,有機溶劑處理 層奈米碳管膜為-均勻的膜狀結構。有機溶劑處理後,奈 米碳管結構的黏性降低,更利於使用。 所述不米兔官拉膜及其製備方法具體請參見范守善等人於 2007年2月12日申請的,於誦年8月16日公開的第 TW200833862號台灣公開專利申請“奈米碳管膜結構及其製備 方法,,。為節省肺,僅制於此,但上射請所有技術揭露也 應視為本發明申請技術揭露的—部分。 (-)田4奈米碳管結構包括至少一奈米碳管礙壓膜,該奈 采石反官結構的製備方法包括以下步驟: ” f先’提供-奈米碳管陣列形成於—生長基底,該陣列為定 25 201039678 - 向排列的奈米碳管陣列。 奈米碳管_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_的製備方法相同。 其次’ _-施壓裝置,擠壓上述奈米翁陣舰得一奈米 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。施壓的 過財,奈米碳管_於壓力的作用下會與生長基底分離 ,從而 ❹形成由複數個奈米碳管組成的具有自支樓結構的奈米碳管礙壓 膜’且所述的複數個奈米碳管基本上與奈米碳管礙壓膜的表面平 行。 本發明實施例中’施難置為_壓頭,_表面光滑,壓頭 的形狀及祕純蚊製備时錢管贼财奈料管的排列 方式。具體地,當採用平面壓頭沿垂直於上述奈米碳管陣列生長 基底的方向擠壓時,可獲得各向同性的奈米碳管礙壓膜;當採用 Ο 滾軸狀壓頭沿某一固定方向碾壓時,可獲得奈米碳管沿該固定方 向取向排列的奈米碳管礙壓膜·,當採用滾軸狀壓頭沿不同方向礙 壓時,可獲得奈米碳管沿不同方向取向排列的奈米碳管儀壓膜。 可理解,當採用上述不同方式擠壓上述的奈米碳管陣列時, 奈米碳管會於壓力的作用下傾倒,並與相鄰的奈米碳管通過凡德 瓦爾力相互吸引、連接形成由複數個奈米碳管組成的具有自支撐 結構的奈米碳管碾壓膜。所述的複數個奈米碳管與該生長基底的 表面成一夾角β,其中,β大於等於零度且小於等於15度 26 201039678 -(GK15°)。依祕㈣方#同’該奈米碳管碰财的奈米石炭 管可沿-固定方向擇優取向排列,請參閱圖1〇;或沿不同方向擇 優取向排列’請參閱圖11。另,在壓力的作用下,奈米破管陣列 會與生長的基底分離,從而使得該奈米碳管碾壓膜容易與基底脫 離’從而形成一自支撐的奈米碳管礙壓膜。 本技術領域技術人員應明白,上述奈米碳管陣列的傾倒程度 與壓力的大小有關,壓力越大,傾肖(即奈米碳管與奈米碳管陣 〇 列生長方向的夾角)越大。製備的奈米碳管碾壓膜的厚度取決於 奈米碳管陣_高度及壓力大小。奈米碳管_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 米碳管陣刺冑度越杨杨雜力越大,職備的絲碳管礙 麗膜的厚度越小。該奈米碳管礙墨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的厚度為工 ◎ 微米~2毫米。 上述奈米碳管碾壓膜中包括複數個沿同一方向或擇優取向排 列的奈米碳管,所述奈米碳管之間通過凡德瓦爾力相互吸引,故, 該奈米碳管碾壓膜具有很好的韌性。該奈米碳管碾壓膜中,奈米 碳管均勻分佈,規則排列。 可理解,該奈米碳管碾壓膜具有一定的厚度,且通過奈米碳 管陣列的高度及壓力大小可控制其厚度。故,該奈米碳管碾壓膜 可直接作為一奈米碳管結構使用。另,可將至少兩層奈米破管碾 27 201039678 . 壓膜層迭設置或併排設置形成一奈米碳管結構。 該奈米碳管賴财奈米碳f的纽大於5()微米。所述奈米 碳管礙壓膜及其製備方法具體請參見范守善等人於丽年6月29 曰申明的’於2009年1月1曰公開的第TW2〇〇9〇〇348號台灣專 利申請“奈米礙管薄膜的製備方法’,。為節省篇幅,僅引用於 此’但上述巾請所有技術揭露也應視為本發日財請技術揭露的一 部分。 〇 (三)#該奈米營結構包括至少-奈料管絮化膜時,該 奈米碳管結構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 電錄電沈積法或雷射蒸發沈積法等各種方法製備的奈米碳管。 —本實關中’採用刀片或其他卫具將上述定向排列的奈米碳 管陣列從基底雜,獲得-奈米碳管祕。優選地,所述的奈米 Ο 碳管原料中,奈米碳管的長度大於100微米。 其次,將上述奈米碳管原料添加到—溶射並進行絮化處理 獲仔-奈米碳官絮狀結構,將上述奈米碳管絮狀結構從溶劑中分 離’並對該奈米碳管絮狀結構定型處朗獲得-奈米碳管膜。 本發明實施例中,溶劑可選用水、易揮發的有機溶劑等。絮 化處理可通過採用超聲波分散處理或高強度授拌等方法。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 管具ir極大_表面積,相賴_奈料管之間具有較大的凡 28 201039678 - 德瓦爾力。上述絮化處理並不會將該奈米碳管原料中的奈米碳管 完全分散於溶劑中,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 遽紙的漏斗中;靜置乾燥-段時間從而獲得—分離的奈米碳管絮 狀結構’圖17為該奈米碳管絮狀結構的照片。 〇 本發明實施射,所義奈米碳管絮狀結構的定型處理過程 具體包括以下步驟:將上述奈米碳管絮狀結構置於一容器中;將 該奈米碳管f狀結構按照預定形狀攤開;施加—定壓力於雜開的 奈米碳管f狀結構;及,將該奈純管絮狀結構巾殘留的溶劑供 乾或等溶劑自然揮發後獲得一奈米碳管絮化膜。 可理解,本㈣實_可_鋪該絲碳管絮狀結構攤開 的面積來控制該奈米碳管絮化膜的厚度和面密度。奈米礙管絮狀 〇結構攤開的面積越大,則該奈米礙管絮化膜的厚度和面密度就越 小。本發明實施例巾麟的奈米碳管絮化麟厚度為1微米〜2毫 米。 ’、 …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 通過柚遽的方式實現,具體包括以下步驟:提供一微孔據膜及一 抽氣漏斗;將上述含有奈米碳管餘結構舰過_孔舰 倒入雜氣漏斗中;減並乾雜獲得一奈米碳管絮化膜。該微 孔遽膜為—表面光滑、孔徑為G.22微米的顏。由於抽濾方^本 29 201039678 ' 身將提供一較大的氣壓作用於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一均勻的奈米碳管絮化膜。且,由 於微孔濾膜表面光滑,該奈米碳管絮化膜容易剝離,得到一自支 撐的奈米碳管絮化膜。 請參見圖12,上述奈米碳管絮化膜中包括相互纏繞的奈米碳 官,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,故’該奈米碳管絮化膜具有很好的韌性。該奈米碳管 Ο 絮倾巾,奈米碳管羽分佈’無酬翻,使得該奈米碳管絮 化膜各向同性。 ' 可理解,該奈米碳管絮化膜具有—定的厚度,且通過控制該 奈米碳管絮狀結構攤開的面積及壓力大小可控制其厚度。故,該 奈米破管絮化膜可直接作為-奈米碳管結構使用。另,可將至少 兩層奈米碳管絮化膜層迭設置或併排設置形成—奈米碳管結構。 所述奈米碳管絮化麟面積及厚度均不限,厚度為丨微米〜丄 〇 毫米’優選為100微来。所述奈米碳管絮化膜及其製備方法具體 請參見范守善等人於2007年5月U日申請的,於細年u月 16曰公開的第TW200844041號台灣專利申請“奈米碳管薄膜的 製備方法”。觸錢幅,刻此,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。 (四)當該奈米碳管結構包括至少—奈米碳管線狀結構時, 該奈米碳管結構的製備方法包括以下步驟: 首先,提供至少一奈米碳管拉膜。 30 201039678 形:=,成方法與步驟㈠中奈米碳管-的 :、处里4、米碳官拉膜,形成至少—奈米碳管線。 該處縣料的步财為_有齡舰 ==得到—非扭轉的奈米碳管線,或為採用轉 “:只兔5拉膜,從而得到—扭轉的奈米碳管線。 Ο Ο 採用有機4丨處理該奈米碳管㈣的倾具縣:將 劑&潤所述奈米碳管杈 機/奋 產生的表面張力二=ΓΓ在揮發性有機溶劑揮發時 太 下,不未碳管拉膜中的相互平行的複數個 通觀德瓦爾力緊密結合,從而使奈祕管拉膜收 非扭轉的絲碳管線。财齡麟揮發财機輔,如乙醇= :醇、丙_、二氣乙燒或氯仿,本實施例中採用乙醇。通過有 〜 1處理_轉奈米碳管線與未經有機溶織理的奈米碳管拉 =::咖積減小’黏性降低。可理解,該採用有機溶劑處 不、只石反官拉膜形成非扭轉的奈米碳管線的方法與步驟(㈠中 採用有機溶劑降低奈米碳管拉膜的黏性的方法相似,其區別在 於^需要形成雜轉的奈米碳管線時,奈米碳管拉朗兩端不 固疋’即不將奈米碳管減設置於基絲面雜架結構上。 、採用機械外力扭轉該奈米碳管拉膜的步驟為採用一機械力將 =述奈米碳官膜兩端沿相反方向扭轉。本發明實施例中,且體可 提供:個騎可齡奈米碳管拉__軸1雜紗轴的尾部 與奈米奴官_結合後,將該紡紗細_的方式旋轉該奈米碳 201039678 •管拉膜’形成-扭轉的奈米碳管線。可理解,上述纺紗軸的旋轉 方式不限,可正轉’也可反轉,或者正轉和反轉相結合。 一當該奈米碳管_的面積為4英寸時,製備的扭轉的奈米碳 官線或非轉的奈米碳管朗紐為10微米〜綱微米。進一步 地,可採用-揮發性有機溶織_扭_奈米碳管線。在揮發 性有機溶劑揮如夺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緊密結合,使扭轉的 〇 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。 所述奈米碳管線及其製備方法具體請參見范守善等人於2〇〇2 年11月5日申請的,於2008年U月21日公告的第13〇3239號台 灣公告專利“一種奈米碳管繩及其製造方法,,,及於於2〇〇5年 12月16日申請的,於2007年7月i日公開的第胃〇〇724486 號台灣公開專利申請“奈米碳管絲及其製作方法,,。為節省篇 〇巾田’僅個於此’但上述中請所有技術揭露也應視為本發明申請 技術揭露的一部分。 再次,利用上述奈米碳管線製備至少一奈米碳管線狀結構, 並得到一奈米碳管結構。 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線狀結構使用。另,可將複數個奈米 碳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 行排列的複數個奈米碳管線經一扭轉步驟得到一絞線結構的奈米 32 201039678 碳管線狀結構。進-步地’可_複數個奈米碳f線或奈米碳管 線狀結構相互平行設置、交叉設置或顿成—層狀的奈米碳管結 構。 乂驟Sl〇2 ’提供一線狀支撐結構2〇2,並將該奈米破管結構 設置於該線狀支撐結構202的表面。 所述線狀支撐結構202用於支樓奈米碳管結構,其材料可為 硬ί·生材料,如.陶究、玻璃、樹脂、石英等,亦可選擇柔性材料, 〇如:塑膠或柔性纖維等。本實施例優選的線狀支撐結構观為— 陶瓷桿。 ❹ 、將上述奈米碳管結構設置於所述線狀支躲構202表面的方 去為·由於奈鱗管結構具有黏性,故,可將—奈米碳管結構直 接纏繞或包裹於所述線狀支撐結構2〇2表面,並通過其黏性固定 於線狀支撐結構2〇2表面。或者,也可通過黏結劑將_奈米碳管 結構固定於_線狀支撐結構2〇2表面。所述黏結劑為石夕膠。 可解所述奈米碳官結構的設置方式與該奈米碳管結構的 2結構«。當奈米碳管結構包括奈米碳管拉職奈米碳管礙 2 ’且Μ碳管賴財奈米碳管沿同―方向或不同方向擇優 撐奈米碳管’的部分奈米碳管由線狀支 =太半一—端向另1排列。當奈米碳管結構包括絮化膜或 =不未石反官賴膜,且奈米碳管賴膜中奈米碳管各向同性 =二樣⑽結她樹;彳秘。爾魏 未㈣線狀結構時,可將單辦米碳管雜結構_於線狀支樓 33 201039678 -結構202的表面或將複數個奈米碳管線狀結構平行、交叉或編織 設置成-層狀奈米碳管結構後,再包裹於線狀支撐結構2〇2的表 面。可理解’當將魏個奈米碳管線狀結構平行設置於線狀支撐 結構202的表面時,奈米竣管線狀結構需沿線狀支撐結構202的 長度方向設置。 、,本實化例十’奈米碳管結構採用重疊且交叉設置的卿層奈 米碳管拉膜,相鄰兩層奈米碳管拉膜之間交叉的角度為90度。該 〇⑽層奈米碳管拉膜的厚度為3⑻微米。糊奈米碳管結構本身的 黏性’將該奈米碳管結構包裹於所述線狀支撐結構202的表面。 '步在將奈米碳官結構設置於線狀支樓結構202的表面 之前’還可形成-熱反射層21時線狀支撐結構2〇2的表面。於 線狀支撐結構2〇2的表面形成—熱反射層加的方法包括塗覆及 經膜中的-種或多種。所述熱反射層21〇的材料為一白色絕 料’如:金屬氧化物、金屬贱陶找。本實施财,熱反射層 〇 210材料優選為三氧化二銘,其厚度為咖微米。 步驟Sl〇3,間隔形成兩個電極,並將該兩個電極挪分 別與該奈米碳管結構形成電連接。 77 π太所^的兩個電極2〇6的設置方式與奈米碳管結構有關,需保 證奈米碳管結構中的部分奈米碳管沿著其中-_極2〇6向另— 個電極206的方向延伸。 为 所述的兩個電極施可設置於奈米碳管結構 不同表* l· 。 卸上且兩個電極2〇6環繞設置於奈米碳管結構的表面。 34 201039678 ’、中兩個電極206間隔設置,以使奈米碳管結構應用於線熱源 2〇時接人—定的_敎贿縣姐。奈米碳管結構本身有很 好的黏附性與導電性,故電極观可與奈米碳管結構之間形成很 好的電接觸。 所述電極206為導電薄膜、金屬片或者金屬引線。該導電薄 、的材料可為金屬、合金、鋼錫氧化物(⑽)、錄锡氧化物⑽〇)、On the π-f-transfer structure, the above-mentioned community can be infiltrated into a container containing an organic solvent by dropping the organic solvent by fresh == the valve wheel carbon ceramics, enamel. After the carbon nanotube ▲ organic solvent infiltration treatment, when the number of layers of the carbon nanotube film is small, the adjacent carbon nanotubes in the nanocarbon tube film shrinks into an interval distribution under the action of the surface. The non-carbon pipeline. When the number of layers of the carbon nanotube film is large, the organic solvent-treated layer of the carbon nanotube film is a uniform film structure. After the organic solvent treatment, the viscosity of the carbon nanotube structure is lowered, which is more conducive to use. For details, please refer to the Taiwan Patent Application No. TW200833862, which was filed on February 12, 2007 by Fan Shoushan et al. The structure and the preparation method thereof, in order to save the lungs, are only made here, but all the technical disclosures of the above-mentioned shots should also be regarded as part of the technology disclosed in the application of the present invention. (-) The field 4 carbon nanotube structure includes at least one The carbon nanotube blocking film, the preparation method of the nepheline sinus structure comprises the following steps: "f first" providing - a carbon nanotube array formed on the growth substrate, the array is set to 25 201039678 - Carbon tube array. The carbon nanotubes are preferably - super-aligned arrays of carbon nanotubes. The carbon nanotube array is prepared in the same manner as the above carbon nanotubes. Secondly, the _-pressure device squeezes the nanometer-shaped ship to obtain a nanometer carbon tube laminated film. The specific process is as follows: The pressure device applies a predetermined pressure to the above-mentioned carbon nanotubes. The pressure of the pressure, the carbon nanotubes _ under the action of pressure will be separated from the growth substrate, thereby forming a nano-carbon tube barrier film composed of a plurality of carbon nanotubes with a self-supporting structure. The plurality of carbon nanotubes are substantially parallel to the surface of the carbon nanotube barrier film. In the embodiment of the present invention, the 'difficulty set is _ indenter, the surface of the _ is smooth, the shape of the indenter, and the arrangement of the money tube thief in the preparation of the pure mosquito. Specifically, when a planar indenter is pressed in a direction perpendicular to the growth substrate of the carbon nanotube array, an isotropic carbon nanotube film can be obtained; when a crucible indenter is used along a certain When the roller is pressed in a fixed direction, a carbon nanotube film which is aligned along the fixed direction of the carbon nanotubes can be obtained. When the roller-shaped indenter is pressed in different directions, the carbon nanotubes can be obtained differently. A carbon nanotube metering film oriented in the orientation direction. It can be understood that when the above-mentioned carbon nanotube array is extruded by the above different methods, the carbon nanotubes are poured under the action of pressure and are attracted and connected with the adjacent carbon nanotubes through the van der Waals force. A carbon nanotube laminated film having a self-supporting structure composed of a plurality of carbon nanotubes. The plurality of carbon nanotubes form an angle β with the surface of the growth substrate, wherein β is greater than or equal to zero degrees and less than or equal to 15 degrees 26 201039678 - (GK15°). According to the secret (four) side #同' the carbon nanotubes of the nano carbon tube can be arranged in a preferred orientation along the fixed direction, please refer to Figure 1〇; or in different directions to choose the preferred orientation ‘see Figure 11. In addition, under the action of pressure, the nanotube array is separated from the grown substrate, so that the carbon nanotube film is easily separated from the substrate to form a self-supporting carbon nanotube film. Those skilled in the art should understand that the degree of tilting of the above-mentioned carbon nanotube array is related to the magnitude of the pressure. The greater the pressure, the larger the angle between the carbon nanotubes and the growth direction of the carbon nanotube array. . The thickness of the prepared carbon nanotube rolled film depends on the size of the carbon nanotube array _ height and pressure. The higher the height of the carbon nanotube _ and the lower the applied pressure, the greater the thickness of the prepared carbon nanotube rolled film; on the contrary, the more the carbon nanotube array has the higher the capacity of the poplar, the more The thickness of the wire carbon tube is less. The width of the carbon nanotube film is related to the size of the substrate grown by the carbon nanotube array. The length of the carbon nanotube film is not limited and can be obtained according to actual needs. The thickness of the carbon nanotube rolled film obtained in the embodiment of the present invention is ◎ micrometers to 2 mm. The carbon nanotube rolled film includes a plurality of carbon nanotubes arranged in the same direction or in a preferred orientation, and the carbon nanotubes are mutually attracted by the van der Waals force, so the carbon nanotubes are crushed. The film has good toughness. In the carbon nanotube rolled film, the carbon nanotubes are evenly distributed and regularly arranged. It can be understood that the carbon nanotube rolled film has a certain thickness, and the thickness can be controlled by the height and pressure of the carbon nanotube array. Therefore, the carbon nanotube rolled film can be directly used as a carbon nanotube structure. Alternatively, at least two layers of nanotubes can be milled 27 201039678. The laminates are stacked or arranged side by side to form a carbon nanotube structure. The carbon nanotubes of the carbon nanotubes are more than 5 () micrometers. For details of the nano-carbon tube pressure-suppressing film and its preparation method, please refer to the Taiwan Patent Application No. TW2〇〇9〇〇348 published by Fan Shou-shan and others on June 29, 2009. "Preparation method of nano film film", in order to save space, only quoted here's but all the technical disclosures of the above-mentioned towels should also be regarded as part of the technical disclosure of this issue. 〇(三)#The nano When the battalion structure comprises at least a gas tube membrane, the preparation method of the carbon nanotube structure comprises the following steps: First, a carbon nanotube raw material is provided. The carbon nanotube raw material may be obtained by chemical vapor deposition. Carbon nanotubes prepared by various methods such as method, graphite electrode constant current electro-deposition electrodeposition or laser evaporative deposition method. - This is a practical example of using a blade or other guard to orient the aligned carbon nanotube array from the substrate. Preferably, in the nano-carbon tube raw material, the length of the carbon nanotubes is greater than 100 micrometers. Secondly, the above-mentioned carbon nanotube raw materials are added to -solute and flocculated. Treatment of the larvae-nano carbon official floc structure , the above-mentioned carbon nanotube floc structure is separated from the solvent and the carbon nanotube film is obtained by shaping the carbon nanotube floc structure. In the embodiment of the invention, the solvent is optional, and the solvent is optional. Organic solvent, etc. The flocculation treatment can be carried out by using ultrasonic dispersion treatment or high-strength mixing, etc. Preferably, the embodiment of the present invention uses ultrasonic dispersion for 1 minute to 3 minutes. Since the carbon nanotube has an ir max _ surface area, Depend on _ between the tube has a large number of 28 201039678 - Devalli. The above flocculation does not completely disperse the carbon nanotubes in the carbon nanotube raw material in the solvent, the carbon nanotubes The method for separating the carbon nanotube floc structure in the embodiment of the present invention specifically includes the following steps: the above-mentioned carbon nanotube containing floc The solvent of the structure is poured into a funnel in which the paper is placed; the drying is allowed to dry for a period of time to obtain a separated carbon nanotube floc structure. FIG. 17 is a photograph of the nano carbon tube floc structure. Implementing shooting The shaping process of the carbon tube floc structure comprises the following steps: placing the above-mentioned carbon nanotube floc structure in a container; spreading the carbon tube f-shaped structure according to a predetermined shape; applying-setting pressure to a heterogeneous carbon nanotube f-like structure; and, a solvent remaining in the neat pure tube floc structure towel or a natural solvent of a solvent to obtain a carbon nanotube flocculation film. It is understood that this (four) real_ The thickness of the carbon nanotube flocculation film and the areal density can be controlled by the area of the carbon fiber floc structure. The larger the area of the floc structure, the larger the area is. The thickness and the areal density of the tube flocculation film are smaller. In the embodiment of the invention, the carbon nanotubes of the Linlin have a thickness of 1 micrometer to 2 mm. ', ..., the separation and shaping treatment of the carbon nanotubes The step of the structure can also be directly realized by the method of pomelo, specifically comprising the steps of: providing a microporous membrane and an extraction funnel; and pouring the above-mentioned carbon nanotube residual structure ship into the miscellaneous funnel Medium; subtracted and dry mixed to obtain a carbon nanotube flocculation membrane. The microporous membrane is a surface having a smooth surface and a pore diameter of G.22 μm. Since the pumping filter 29 201039678 's body will provide a large air pressure on the nano carbon tube floc structure, the carbon nanotube floc structure will directly form a uniform carbon nanotube floc. Film. Moreover, since the surface of the microporous membrane is smooth, the carbon nanotube flocculation membrane is easily peeled off, and a self-supporting carbon nanotube flocculation membrane is obtained. Referring to FIG. 12, the carbon nanotube film of the above-mentioned carbon nanotubes comprises intertwined nano carbon officials, and the carbon nanotubes are attracted and entangled by van der Waals force to form a network structure, so that The carbon nanotube film has good toughness. The carbon nanotube Ο 倾 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , It is understood that the carbon nanotube flocculation membrane has a constant thickness, and the thickness can be controlled by controlling the area and pressure of the carbon nanotube floc structure. Therefore, the nano tube breaking film can be directly used as a carbon nanotube structure. Alternatively, at least two layers of carbon nanotube flocculation membranes may be stacked or arranged side by side to form a carbon nanotube structure. The carbon nanotubes of the carbon nanotubes are not limited in area and thickness, and the thickness is 丨 micrometers to 丄 〇 mm Å is preferably 100 micrometers. For the details of the carbon nanotube film and the preparation method thereof, please refer to the patent application "Nano Carbon Tube Film" of the TW200844041 published by Fan Shoushan et al. in May 2007. Preparation method". Touching the money, in this regard, but all the technical disclosure of the above application should also be considered as part of the technical disclosure of the present application. (4) When the carbon nanotube structure comprises at least a nanocarbon line-like structure, the method for preparing the carbon nanotube structure comprises the following steps: First, at least one carbon nanotube film is provided. 30 201039678 Shape: =, into the method and step (a) in the carbon nanotubes -:, 4, m carbon official film, forming at least - nano carbon pipeline. The position of the county is _ ageing ship == get - non-twisted nano carbon pipeline, or use the transfer ": rabbit 5 film, thus get - twisted nano carbon pipeline. Ο Ο organic 4丨The treatment of the carbon nanotubes (4) of the dumping county: the agent & the surface of the carbon nanotubes / machine generated by the surface tension two = ΓΓ when the volatile organic solvent volatilization is too low, not carbon tube The plurality of through-view Deval forces in parallel with each other in the film are tightly combined, so that the Nylon tube draws a non-twisted silk carbon line. The commemorative pharmacy, such as ethanol =: alcohol, propylene _, two gas Ethylene or chloroform, ethanol is used in this embodiment. By using ~1 treatment _ turn nano carbon line and carbon nanotubes without organic solution weaving =:: coffee product reduces 'viscosity reduction. Understandable The method and the step of forming a non-twisted nanocarbon pipeline by using an organic solvent, and only a stone reversed film is similar to the method of using an organic solvent to reduce the viscosity of the carbon nanotube film. The difference is that When it is necessary to form a hetero-nano carbon line, the carbon nanotubes are not solid at both ends, that is, the carbon is not carbonized. The step of twisting the carbon nanotube film by using a mechanical external force is to twist the both ends of the carbon film in the opposite direction by a mechanical force. In the embodiment of the invention And the body can provide: a ride on the aged carbon nanotubes __ shaft 1 the end of the yarn shaft and the nano slave official _ combined, the spinning fine _ the way to rotate the nano carbon 201039678 • tube pull The film 'forms-twisted nano carbon line. It can be understood that the above-mentioned spinning shaft can be rotated in any way, and can be rotated forward or reversed, or combined with forward rotation and reverse rotation. When the area is 4 inches, the prepared twisted nano carbon official line or the non-transformed nano carbon tube is 10 micrometers to less micrometers. Further, it can be used - volatile organic solvent-woven _ twisted-nano carbon Pipeline. Under the action of the surface tension generated by the volatile organic solvent, the adjacent carbon nanotubes in the treated twisted nanocarbon pipeline are tightly bonded by van der Waals force to make the twisted nanocarbon Reduced specific surface area of the pipeline, reduced impurities, and twisted nanocarbon without organic solvent treatment The density and strength of the pipeline are increased. The specific description of the nanocarbon pipeline and its preparation method can be found in Fan Shoushan et al. on November 5, 2002, and the 13th announced on May 21, 2008. 〇3239 Taiwan Announcement Patent “A nano carbon tube rope and its manufacturing method, and, as applied on December 16, 2005, the first stomach 724486 published on July i, 2007 Taiwan's published patent application "Nano Carbon Tube and its manufacturing method, in order to save the article "only in this", but all the technical disclosures mentioned above should also be regarded as part of the technical disclosure of the present application. The at least one nano carbon pipeline structure is prepared by using the above nano carbon pipeline, and a carbon nanotube structure is obtained. The twisted nano carbon pipeline or the non-twisted nano carbon pipeline is a self-supporting structure, which can be directly used as a Nano carbon line structure is used. In addition, a plurality of nano carbon pipelines may be arranged in parallel to form a bundle-structured nanocarbon line-like structure, or the parallel array of plurality of carbon carbon pipelines may be subjected to a twisting step to obtain a stranded structure of nano 32 201039678 Carbon line structure. The step-by-step can be a plurality of nano-carbon f-lines or nano-carbon tubes. The linear structures are arranged in parallel with each other, cross-arranged or formed into a layered carbon nanotube structure. The step S1〇2' provides a linear support structure 2〇2, and the nano-tube structure is disposed on the surface of the linear support structure 202. The linear support structure 202 is used for a bridge carbon nanotube structure, and the material thereof may be a hard material, such as ceramics, glass, resin, quartz, etc., or a flexible material, such as plastic or Flexible fiber, etc. A preferred linear support structure for this embodiment is a ceramic rod. 、 设置 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , The surface of the linear support structure 2〇2 is fixed to the surface of the linear support structure 2〇2 by its adhesiveness. Alternatively, the carbon nanotube structure may be fixed to the surface of the _ linear support structure 2〇2 by a binder. The binder is Shishi gum. The arrangement of the carbon carbon structure and the structure 2 of the carbon nanotube structure can be solved. When the carbon nanotube structure includes the carbon nanotubes of the carbon nanotubes, the carbon nanotubes of the carbon nanotubes are in the same direction and the carbon nanotubes of the carbon nanotubes are selected along the same direction or in different directions. From the line branch = too half one - the end is arranged to the other one. When the carbon nanotube structure includes a flocculation membrane or a non-stone anti-detonation membrane, and the carbon nanotubes in the nano-carbon nanotubes are isotropic = two (10) knot her tree; In the case of the Weiweiwei (4) linear structure, the surface of the single carbon nanotubes may be arranged in a line-shaped branch 33 201039678 - the surface of the structure 202 or a plurality of nanocarbon line-like structures may be parallel, crossed or woven into a layer After the carbon nanotube structure is formed, it is wrapped around the surface of the linear support structure 2〇2. It can be understood that when the Wei-nanocarbon carbon line-like structure is disposed in parallel on the surface of the linear support structure 202, the nano-tube-like structure needs to be disposed along the length direction of the linear support structure 202. The tenth carbon nanotube structure of the present embodiment adopts overlapping and intersecting layers of the carbon nanotube film, and the angle between the adjacent two layers of carbon nanotube film is 90 degrees. The thickness of the ruthenium (10) layer carbon nanotube film is 3 (8) microns. The viscosity of the paste carbon nanotube structure itself encapsulates the carbon nanotube structure on the surface of the linear support structure 202. The step of forming the surface of the linear support structure 2〇2 when the heat reflective layer 21 is formed may be formed before the surface of the linear branch structure 202 is disposed. Forming on the surface of the linear support structure 2〇2—the method of applying the heat reflective layer includes coating or one or more of the transmembrane. The material of the heat reflecting layer 21 is a white material such as a metal oxide or a metal enamel. In the implementation, the heat-reflecting layer 〇 210 material is preferably bismuth trioxide, and the thickness thereof is a micron. In step S10, two electrodes are formed at intervals, and the two electrodes are electrically connected to the carbon nanotube structure. The arrangement of the two electrodes 2〇6 of 77 π太所^ is related to the structure of the carbon nanotubes. It is necessary to ensure that some of the carbon nanotubes in the carbon nanotube structure are along the -_ pole 2〇6 to the other The direction of the electrode 206 extends. The two electrodes can be placed on different configurations of the carbon nanotube structure* l· . Unloaded and the two electrodes 2〇6 are disposed around the surface of the carbon nanotube structure. 34 201039678 ', the two electrodes 206 are spaced apart, so that the carbon nanotube structure is applied to the line heat source 2 〇 _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ The carbon nanotube structure itself has good adhesion and electrical conductivity, so the electrode view can form a good electrical contact with the carbon nanotube structure. The electrode 206 is a conductive film, a metal sheet or a metal lead. The conductive thin material may be metal, alloy, steel tin oxide ((10)), tin oxide (10) 、),

導2銀勝、導電聚合轉。該導電薄膜可通過物理氣相沈積法, ^子氣相沈積法或其他方法軸於奈米碳管結構表面。該金屬片 :為銅片或銘片等。該金屬片或者金屬引線可通過導電黏結劑固 j奈米碳管結構表面。本實施财,_贿法分別於該奈米 W結構表面沈積兩她卿為雜m,然後職兩她膜分別 與—導電引線電連接。 所述電極2G6還可為—金屬性奈米碳管結構。該奈米碳管結 山,括疋向剩胸勻分佈的金屬性奈米碳管。具體地,該奈米 。構包括至奈米碳管拉膜或至少_奈米碳管線。優選 也將兩個奈米碳管拉膜分別設置於沿線狀支撐結構观長度方 向的兩端作為電極2〇6。 理解’本實施财’射先於奈米碳管結構絲面形成兩 、'仃且間隔β又置的電極206,且該電極·與奈米碳管結構電連 。然後,將該形成㈣極206的奈米碳管結構設置於上述線狀 撐結構2〇2的表面。在形成兩個電極後,可進一步形成兩 條導電引線,分別從兩個電極施仙至外部電源。 35 201039678 - 步驟S104,提供一基體材料預製體,並將基體材料預製體與 奈米碳管結構複合,形成一奈米碳管複合結構。 所述基體材料預製體可為基體材料所形成的溶液或製備該基 體材料的前驅反應物。該基體材料預製體於一定溫度下應為液離、 或氣態。所述將基體材料預製體與奈米碳管結構複合的方法包括 塗覆,沈積,印刷,浸潰及喷塗中的一種或多種。 所述基體材料包括高分子材料或非金屬材料等。具體地,該 〇 高分子材料可包括熱塑性聚合物或熱固性聚合物令的一種或多 種’故該紐㈣賴體可為线該熱齡聚合物或触性聚合 物的聚合物單體溶液’或該熱塑性聚合物或熱固性聚合物在揮發 性有機溶射溶職形觸齡液。該非金騎料可包括玻璃、 陶曼及半導體材料中的-種或多種,故該基體材料預製體可為 金屬材料難製成的雜、製備該非金屬材料的反應氣體或呈氣 態的該非金屬材料。具體地,可採用真空蒸鍍、雜、化學氣相 〇 =積yCVD)及物理氣相沈積(PVD)的方法形成氣態的基體材 料預製體’並使該基體材料賴體沈積於奈米碳管結構的奈米碳 e表面。另’可將大量非金屬材料顆粒分散於溶劑中,形成一聚 料作為該基體材料預製體。 田"亥基體材料雜料贿時,可通過將該液態基體材料預 製體π顺奈米碳管結構及固化該基體材料預製體,從而使該基 體材料錢至該奈米碳管結構的微孔+,形成—奈米碳管複合結 構’當該基體㈣賴H為氣‘_,可將該基體材料預製體沈積 36 201039678 於奈米碳官結構中的奈米碳管表面,從而使該基體材料充滿該奈 米碳管結構的微孔t ’形成-奈米碳管複合轉。當該基體材料 預製體為聚料時’可通過塗覆'喷塗等方法與該奈米碳管結構形 成複合結構。 本實施例採用注膠法將高分子材料與奈米碳管結構複合,形 成奈米石炭官複合結構’請參閱圖1S,該方法具體包括以下步驟: 步驟S1041 :提供一液態熱固性高分子材料。 〇 所述液態熱固性高分子材料的黏度低於5帕•秒,並能於室 溫下保持該黏度30分鐘以上。所述熱固性高分子材料包括高分子 材料和固化劑、改性劑、填料或者稀釋劑等添加物。其中,高分 子材料的含量占所述熱固性高分子材料質量的7〇%〜95%,所述添 加物的含量㈣述麵性高分子將f量的5%〜拠。所述高分 ^材料為祕樹脂、環輪脂、雙絲醯亞胺_、聚苯並惡嗓 曰氰酸8曰树月曰、聚醯亞胺樹脂、聚氨醋、聚甲基丙稀酸甲酯 G和不飽和聚醯樹脂等中一種或者幾種混合。所述固化劑用於促進 所述熱固性高分子材料的固化,其包括脂肪胺、脂環胺、芳香胺、 聚酿胺、酸肝、樹脂類和叔胺巾—種或者幾種混合。所述改性劑 2改善所述熱陳高分子材料㈣性、抗剪、抗彎、抗冲或者 :邑緣f生等。常用改性劑包括聚硫橡膠、聚醯胺樹脂、聚乙婦 ^叔丁料者Tit轉射-種或者幾種混合。職填料用於改 善所述熱m性高分子材湘化時的散祕件,轉料也可減少所 述熱固性高分子材料的用量,降低成本。常用填料包括石棉纖維、 37 201039678 - 玻璃纖維、石英粉、莞粉、氧化紹和矽膠粉中一種或者幾種混合。 所述稀釋綱於降低樹脂黏度,改善樹蘭渗透性。所述稀釋劑 包括二縮水甘_、多縮水甘㈣、環氧秘丁基鱗、環氧丙炫 苯基鍵、二魏秘乙細、三環氧秘丙細和烯丙基苯齡中 的一種或者幾種混合。 本發明實_優選⑽氧樹脂製舰祕陳高分子材料, 其具體包括以下步驟: 〇 錢,將縮水甘油㈣環氧和縮水甘油㈣魏的混合物置 於-谷器中,加熱至30。〇60。〇 ’並對容器中所述縮水甘油鍵型環 氧和縮水甘_型魏誠合物勝1()分鐘,直騎述縮水甘油 醚型環氧和縮水甘油醋型環氧的混合物混合均勾為止。 其次’將麟胺和二縮水甘_加人麟述·均勻的縮水 甘油環氧和縮水甘油醋型環氧的混合物中進行化學反應。 最後,騎述縮水甘_型縣和縮水甘油酯型環氧的混合 〇物加熱至3(r〇6(rc:,從而得到—含環氧態翻性高分子 材料。 其步驟Sl〇42:採用所述液態熱固性高分子材料浸潤所述奈米碳 高分子材料朗親奈米碳管結構的方 所述採用液態熱固性 法包括以下步驟: 具中首先,將設置有奈靖結構的線狀支撐結㈣2置於一模 38 201039678 其次,將所述液態熱固性高分子材料注射進所述模具中,浸 潤所述奈米碳管結構。為讓液態熱固性高分子材料充分浸潤所述 奈米碳管結構,浸潤所述奈米碳管結構的時間不能少於1〇分鐘。 本實施例中將100層奈米碳管拉膜層迭包裹於陶瓷桿的表面 後置於模具中。然後將環氧樹脂的液態熱固性高分子材料注射進 所述模具中,浸潤所述奈米碳管結構20分鐘。 可理解,將所述液態熱固性高分子材料浸潤所述奈米碳管結 〇 構的方法不限注射的方法,所述液態熱固性高分子材料還可通過 毛細作用被吸入到所述奈米碳管結構中,浸潤所述奈米碳管結 構’或者騎述奈米碳管結構浸泡於所述液態熱固性高分子材料 t。 步驟S1043 :固化液態熱固性高分子材料,得到一奈米碳管高 分子材料複合結構。 本實施例中’含環氧樹脂的熱固性高分子材料的固化方法具 〇 體包括以下步驟: 首先,通過一加熱裝置將該模具加熱至50。(:〜7(TC,在該溫度 下含環氧樹脂的熱固性高分子材料為液態,維持該溫度丄小時〜3 小時’使付該熱固性高分子材料繼續吸熱以增加其固化度。 士其次,繼續加熱該模具至赃〜1〇〇〇c,在該溫度下維持工小 T 1時使得所述熱JU性高分子材料繼續吸熱以增加其固化度。 ±再次’繼續加熱該模具至赃〜赋,在該溫度下維持2小 時〜20小時’使得所述熱固性高分子材料繼續吸熱以增加其固化 39 201039678 度。 最後’停止加熱,待鋪具降溫至室溫後,脫模可得一奈米 碳管高分子材料複合結構。 可理解,上述方法還可將鋪具一次加熱至赃〜靴進行 固化。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2007年12月16日申請的申請號為9615_的台灣專利申請 “奈米碳管複合材料的製備方法,,。為節省篇幅,刻用於此明 〇 C上述申明所有技術揭露也應視為本發明申請技術揭露的 分。 ,可理解’上述步驟sl〇3中形成電極2〇6的步驟可在步驟細 形成,奈米碳管複合結構之後進行。當絲雜料僅填充於該奈 只炭答、>、。構的微孔中,從而使奈米碳管部分暴露於奈米碳管複合 結構表面時,可採用與步驟測相同的方法將兩個電極206直^ 形成於該奈米碳管複合結構表面,並與奈米碳管結構形成電連 ❹接。當該基體材料全部包覆該奈米碳管結構時,可採用一切割的 步驟=割該奈米碳管複合結構,從而使該奈米碳管結構暴露於奈 米奴官複合結構表面’進而採用與步驟湖相同的方法將該兩個 電極206與暴露出來的奈米碳管結構電連接。 進一步,本實施例還可形成一絕緣保護層208於該加熱元件 2〇4的外表面,並將加熱元件2〇4覆蓋。所述絕緣保護層的材 料為-、%緣轉,如:轉、麟等。所述絕緣保護層厚度 不限’可根據實際情況選擇。本實施例中,該絕緣保護層的 201039678 -材料_橡膠’其厚度為G5毫米。該絕緣保護層观可通過黏結 劑或機械固定的方法固定於加熱元件2〇4表面。另,當該絕緣保 護層208的材料為一熱塑性聚合物時,可將該熱塑性聚合物於高 溫下於融化狀態塗敷或包裹於加熱元件204表面,待低溫時固化 形成該絕雜護層。另,#該絕雜護層為—柔性聚合 物’如-?》笨二m乙二醇g旨(pET)賴時,可通過一献壓步 驟’將該絕緣保護層205與該加熱元件2〇4疊加並熱壓,使絕緣 0 保邊層與加熱元件204牢固結合。 請參見圖19 ’可選擇地,當本發明第—實關中的加熱元件 2〇4為-柔性奈米唉管複合結構時,該線熱源2〇可通過以下方法 製備,具體包括以下步驟: 步驟S401,提供一奈米碳管結構。 /驟S4〇2 ’提供一柔性基體材料預製體,並將柔性基體材料 預製體與奈米碳管結構複合,形成—柔性奈米碳管複合結構。 —步驟湖’提供-線狀讀結構202,並將該柔性奈米碳管 複合結構設置於線狀支撐結構202的表面。 步驟S404,間隔形成兩㈣極,並將該兩個電極挪分 別與該柔性奈米碳管複合結構中的奈米碳管結構形成電連接。刀 〃當奈米碳管結構完全被基體材料包覆時,可進—步通過切割 等方式使該奈米碳管結卿分絲於紐奈米碳管複合結縣 面’從而確保電極206與奈米碳管結構電連接。 可理解’也可預先形成兩個電極施與奈米碳管結構電連接, 201039678 再將奈米碳找構與柔性基體材料賴體複合碱奈米碳管複合 結構。 請參_ 2〇,本發明第二實施例提供一種線熱源3〇,該線熱 源30包括-加熱元件3〇4及兩個電極間隔設置且與該加熱元 件3〇4電連接。該加熱元件3〇4包括一線狀奈米碳管複合結構。 所述線狀奈米碳管複合結構與本發明第一實施例中的所述線狀奈 米碳管複合結構相同。所述線狀奈米碳管複合結構包括至少一奈 〇 米碳管職結構及紐频,所錄歸料滲透崎輕少一夺 米碳管線狀結射。所述奈米碳管線狀結構包括複數個微孔,二 述基體材料料於該絲碳管線聽制微财。所述線狀奈米 碳管複合結_可包括-基體及至少—奈米碳管絲結構複合於 該基體中。可理解’將該奈米碳管線狀結構直接放置於模具中, 然後將液悲細性1¾分子材料注人賴具中浸麵奈米碳管線狀 結構,最後加熱固化即可製備該線狀奈米破管複合結構。所述奈 〇米碳管雜結構及基體㈣與本㈣第—實施财的奈米礙管線 狀結構及基體材料相同。由於奈米碳管線狀結構具有自支撐特 性,該線狀奈米碳管複合結構也具有自支樓特性。所述電極302 可環繞於該線狀奈米碳管複合材料的表面並與所述奈米碳管線狀 結構電連接。所述電極302的材料與本發明第一實施例中的電極 206相同。 所述的線祕及其製備方法具有以下m,由於該奈 米破管結構為-自支雜構’且奈米碳管於奈純管結構中均句 42 201039678 ο 〇 分佈,將該自支撐的奈米碳管結構與基體材料直接複合,可使複 合後形成的加熱元件中奈米碳管仍相互結合保持一奈米碳管結構 的形態,從而使加熱元件中奈米碳管既能均勻分佈形成導電網 絡,又不受奈米碳管於溶液中分散濃度的限制,使奈米碳管於加 熱元件中的質量百分含量可達到99%,使該熱源具有更高的加熱 性能。另’絲體㈣的麵不限於聚合物,使該熱源的應用範 圍更加廣泛。第二,由於奈米碳管具有較好的強度及韌性,奈米 碳管結構的強度較大’纽較好,不易破裂,使其具有較長的使 用壽命’特別的,當該奈米碳管結構與柔性基體材料複合形成加 熱疋件時’可製備—柔性熱源,使該熱源具有更廣的應用範圍。 第三,奈米碳管結構中的奈米碳管均勻分佈,故加熱元件具有 均句的厚度及餘’發熱均自。由於奈米碳麵電熱轉換效率高, 故:該線_具有升溫迅速、m後小、熱交換速度快、轄射效 率门的特點。第四,奈米碳管的餘較小,使得奈米碳管結構可 ^有較小的厚度,可製備微型線熱源,應用於微型器件的加熱。 ^五’當奈米碳管結構包括奈米碳管拉断,該奈米碳管拉膜中 ^卡碳管沿同-方向擇優取向排列,具有較好的導電性能,使該 好的加触能。第六,卿成自支_絲碳管結構, 〜4射結構與基聽料直接複合形成加熱元件的方法簡 複^奈^管在加熱元件㈣含量可方㈣_。與基體材料 ,糊梅碳 43 201039678 綜上所述’本發明確已符合發明專利之要件,遂依法提出專 利申請。惟,以上所述者僅為本發明之較佳實施例,自不能以此 限制本案之申請專職®。舉凡熟悉本紐藝之人士援依本發明 之精神所作之等效修飾化,皆應涵蓋独τ申請柄範圍^。 【圖式簡單說明】 圖1為本發明第一實施例提供的線熱源的結構示意圖。 圖2為圖1的線熱源沿線1141的剖面示意圖。 圖3為圖2的線熱源沿線皿-皿的剖面示意圖。 圖4為本發明第-實施例的線熱源包括層狀奈米碳管複合結 構設置於線狀支獅構表_示意圖,其巾基體材料渗透於夺米 碳管結構中。 圖5為本發明第-實施例的線熱源包括層狀奈米唆管複合結 構設置於線狀支撐結構表面的示意圖,其中奈米碳管結構複人於 基體材料中。 σ ' 圖6為本發明第-實施例的線熱源包括單個線狀奈米碳管複 合結構設置於線狀支撐結構表面的示意圖。 圖7為本發明第-實施例的線熱源包括複數個線狀奈米碳管 複合結構設置於線狀支樓結構表面的示意圖。 圖8為本發明第-實施例的線熱源中的奈米碳管妆膜結構的 掃描電鏡照片。 圖9為圖8中的奈米碳管拉膜結構中的奈米碳管片段的垆構 不意圖。 44 201039678 圖ίο為本發明第-實施綱線熱源中的奈米碳管礙壓膜結構 中的奈米碳管沿同一方向擇優取向排列的掃描電鏡照片。 圖11為本㈣第-實施綱線細、巾奈米碳管碾壓膜結構中 的奈米碳管沿不同方向擇優取向排列的掃描電鏡照片。 圖12為本發明帛-實施例的線熱源中的奈米碳管絮化膜結構 的掃描電鏡照片。 圖13為本發明第一實施例的線熱源中的非扭轉的奈米碳管線 的掃描電鏡照片。 圖Μ為本發明第-實施__財的轉的奈米碳管線的 掃描電鏡照片。 圖15為本發明第-實施例的線熱源中奈米碳管拉膜與環氧樹 脂複合結構的斷面掃描電鏡照片。 圖16為本發明第-實施例線熱源的一種製備方法的流程圖。 圖17為本發明實施例的線熱源的奈米石炭管絮狀結構的照片。 〇 圖18為本發明第—實施例將設置於線狀支撐結構表面的奈米 碳管結構與高分子材料複合的方法的流程圖。 圖19為本發明第-實施例線熱源的另1製備方法的流程 圖。 圖20為本發明第二實施例提供的線熱源的結構示音圖。 【主要元件符號說明】 奈米碳管片段 143 奈米碳管 145 45 201039678 ' 線熱源 20,30 線狀支撐結構 202 加熱元件 204, 304 電極 206,302 絕緣保護層 208 熱反射層 210 基體材料 2042 奈米碳管結構 2044 0 基體 2040 〇 46Guide 2 silver wins, conductive polymerization turn. The conductive film may be axially deposited on the surface of the carbon nanotube structure by physical vapor deposition, sub-vapor deposition or the like. The metal piece is a copper piece or a piece of film or the like. The metal piece or the metal lead can be fixed to the surface of the carbon nanotube structure by a conductive adhesive. In this implementation, the bribe method deposits two herms into the surface of the nano-W structure, and then the two films are electrically connected to the conductive leads. The electrode 2G6 may also be a metallic carbon nanotube structure. The carbon nanotubes are knotted, and the metallic carbon nanotubes are evenly distributed to the remaining chest. Specifically, the nano. The structure includes a carbon nanotube film or at least a nanocarbon line. Preferably, two carbon nanotube film are also respectively disposed at both ends of the linear support structure in the longitudinal direction as the electrode 2?6. It is understood that the 'implementation of the present invention' precedes the surface of the nanocarbon tube structure to form two electrodes, '仃 and spaced apart β, and the electrode is electrically connected to the carbon nanotube structure. Then, the carbon nanotube structure forming the (four) pole 206 is placed on the surface of the above-mentioned linear support structure 2〇2. After the two electrodes are formed, two conductive leads can be further formed, respectively, from the two electrodes to the external power source. 35 201039678 - Step S104, providing a matrix material preform and combining the matrix material preform with the carbon nanotube structure to form a carbon nanotube composite structure. The matrix material preform may be a solution formed of a matrix material or a precursor reactant for preparing the matrix material. The matrix material preform should be in a liquid, or gaseous state at a certain temperature. The method of combining the matrix material preform with the carbon nanotube structure includes one or more of coating, depositing, printing, dipping, and spraying. The base material includes a polymer material or a non-metal material or the like. Specifically, the bismuth polymer material may include one or more of a thermoplastic polymer or a thermosetting polymer, so the ruthenium may be a polymer monomer solution of the thermal age polymer or the haptic polymer' or The thermoplastic polymer or thermosetting polymer is in a volatile organic solvent solution. The non-golden riding material may include one or more of glass, taman and semiconductor materials, so the matrix material preform may be a miscellaneous metal material, a reaction gas for preparing the non-metal material, or a gaseous non-metal material. . Specifically, a vacuum matrix, a chemical vapor phase 积=product CVD, and a physical vapor deposition (PVD) method can be used to form a gaseous matrix precursor preform and deposit the matrix material on the carbon nanotubes. Structure of the nanocarbon e surface. Alternatively, a large amount of non-metallic material particles may be dispersed in a solvent to form a polymer as the matrix material preform. When the field material is brittle, the liquid matrix material can be pre-formed into a π-snap carbon tube structure and the matrix material preform is solidified, so that the matrix material is paid to the micro-carbon nanotube structure. Hole +, forming - carbon nanotube composite structure 'When the substrate (4) is H is gas '_, the matrix material preform can be deposited 36 201039678 on the surface of the carbon nanotube in the carbon carbon structure, thereby making the The matrix material is filled with the microporous t' forming-nanocarbon nanotube composite turn of the carbon nanotube structure. When the base material preform is a polymer, the composite structure can be formed with the carbon nanotube structure by a coating or the like. In this embodiment, the polymer material is composited with the carbon nanotube structure to form a nano-carboniferous composite structure. Referring to FIG. 1S, the method specifically includes the following steps: Step S1041: providing a liquid thermosetting polymer material. 〇 The liquid thermosetting polymer material has a viscosity of less than 5 Pa•sec and can maintain the viscosity for more than 30 minutes at room temperature. The thermosetting polymer material includes a polymer material and an additive such as a curing agent, a modifier, a filler or a diluent. The content of the high molecular material accounts for 7〇% to 95% of the mass of the thermosetting polymer material, and the content of the additive (4) is 5% to f of the amount of f. The high-scoring material is a secret resin, a ring grease, a bismuth imide, a polybenzophthalocyanine 8 eucalyptus, a polyimine resin, a polyurethane, a polymethyl propylene One or a mixture of the acid methyl ester G and the unsaturated polyfluorene resin. The curing agent is used to promote the curing of the thermosetting polymer material, and includes a fatty amine, an alicyclic amine, an aromatic amine, a polyamine, a sour liver, a resin, and a tertiary amine towel, or a mixture thereof. The modifier 2 improves the (four) properties, shear resistance, bending resistance, impact resistance or the like of the thermal polymer material. Commonly used modifiers include polysulfide rubber, polyamidamine resin, Tween tert-butylate Tit-transfer-type or several kinds of mixing. The filler is used to improve the secret parts of the hot m-type polymer material, and the material can also reduce the amount of the thermosetting polymer material and reduce the cost. Commonly used fillers include asbestos fiber, 37 201039678 - glass fiber, quartz powder, Wan powder, oxidized Shao and glutinous rice powder in one or several kinds. The dilution is to reduce the viscosity of the resin and improve the permeability of the orchid. The diluent includes diglycidyl, polyglycidyl (tetra), epoxy butyl butyl sulphate, epoxidized phenyl phenyl bond, dimethicone, triepyl propyl propyl and allyl phenyl age. One or several blends. The present invention is preferably a (10) oxygen resin ship-made polymer material, which specifically comprises the following steps: 〇 Money, a mixture of glycidol (tetra) epoxy and glycidol (tetra) Wei is placed in a --barrel and heated to 30. 〇60. 〇 ' and the mixture of the glycidyl bond type oxygen and the glycidyl sulphate in the container is 1 () minutes, and the mixture of the glycidyl ether epoxy and the glycidol vinegar type epoxy is mixed. Secondly, a chemical reaction is carried out in a mixture of linaloamine and diglycolic acid, and a uniform mixture of glycerin epoxy and glycidol vinegar epoxy. Finally, the mixed mash of the glycosyl-type epoxy and the glycidyl ester epoxy is heated to 3 (r〇6(rc:, thereby obtaining) the epoxy-containing tumbling polymer material. Step S1〇42: The liquid thermosetting method adopts the liquid thermosetting method to infiltrate the nano-carbon polymer material, and the liquid thermosetting method comprises the following steps: First, a linear support knot provided with a Nai Jing structure (4) 2 is placed in a mold 38 201039678 Next, the liquid thermosetting polymer material is injected into the mold to infiltrate the carbon nanotube structure. In order to fully infiltrate the carbon nanotube structure by the liquid thermosetting polymer material, The time for infiltrating the carbon nanotube structure is not less than 1 minute. In this embodiment, a 100-layer carbon nanotube film is laminated on the surface of the ceramic rod and placed in a mold. The liquid thermosetting polymer material is injected into the mold to infiltrate the carbon nanotube structure for 20 minutes. It can be understood that the method of infiltrating the carbon thermosetting polymer material into the carbon nanotube structure is not limited to injection. The liquid thermosetting polymer material may also be sucked into the carbon nanotube structure by capillary action, infiltrating the carbon nanotube structure or immersing the carbon nanotube structure in the liquid thermosetting property. Molecular material t. Step S1043: curing the liquid thermosetting polymer material to obtain a nano carbon tube polymer material composite structure. In the present embodiment, the method for curing the epoxy resin-containing thermosetting polymer material has the following steps: First, the mold is heated to 50 by a heating device. (: 〜7 (TC, at which temperature the thermosetting polymer material containing epoxy resin is in a liquid state, maintaining the temperature for ~3 hours) to make the thermosetting high The molecular material continues to absorb heat to increase its degree of solidification. Secondly, the mold is further heated to 赃~1〇〇〇c, and the heat of the thermal polymer material continues to absorb heat to increase its temperature at this temperature. Degree of cure. ± Again 'continue to heat the mold to 赃~, at this temperature for 2 hours to 20 hours' to allow the thermoset polymer material to continue to absorb heat to increase its 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 For the specific steps of the above-mentioned preparation of the carbon nanotube composite structure, the preparation method of the nano carbon tube composite material of the application No. 9615_, which was filed on Dec. 16, 2007, to the same. In order to save space, the above description of all the technical disclosures should also be regarded as the points disclosed in the technical application of the present invention. It can be understood that the steps of forming the electrodes 2〇6 in the above steps sl3 can be formed in steps. After the nano carbon tube composite structure is carried out, when the silk material is only filled in the micropores of the carbon nanotubes, and the carbon nanotubes are partially exposed to the surface of the carbon nanotube composite structure The two electrodes 206 can be formed directly on the surface of the carbon nanotube composite structure by the same method as the step measurement, and can be electrically connected to the carbon nanotube structure. When the base material completely covers the carbon nanotube structure, a cutting step can be used = cutting the carbon nanotube composite structure, thereby exposing the carbon nanotube structure to the surface of the nano slave structure. The two electrodes 206 are electrically connected to the exposed carbon nanotube structure in the same manner as the step lake. Further, this embodiment can also form an insulating protective layer 208 on the outer surface of the heating element 2〇4 and cover the heating element 2〇4. The material of the insulating protective layer is -, % edge, such as: turn, Lin, and the like. The thickness of the insulating protective layer is not limited to be selected according to actual conditions. In this embodiment, the insulating protective layer of 201039678 - material_rubbery has a thickness of G5 mm. The insulating protective layer can be fixed to the surface of the heating element 2〇4 by a bonding agent or a mechanical fixing method. In addition, when the material of the insulating protective layer 208 is a thermoplastic polymer, the thermoplastic polymer may be coated or wrapped on the surface of the heating element 204 in a molten state at a high temperature, and solidified to form the insulating layer when it is cold. In addition, the insulating layer is a flexible polymer, such as -?, which can be passed through a pressure-preventing step of the insulating protective layer 205 and the heating element. 4 superimposed and hot pressed, so that the insulating 0 edge layer and the heating element 204 are firmly combined. Referring to FIG. 19 'optionally, when the heating element 2〇4 in the first embodiment of the present invention is a flexible nano tube composite structure, the line heat source 2〇 can be prepared by the following method, and specifically includes the following steps: S401, providing a carbon nanotube structure. /S4〇2' provides a flexible matrix material preform, and the flexible matrix material preform is combined with the carbon nanotube structure to form a flexible carbon nanotube composite structure. The step lake provides a linear read structure 202 and the flexible carbon nanotube composite structure is disposed on the surface of the linear support structure 202. Step S404, forming two (four) poles at intervals, and electrically connecting the two electrodes to the carbon nanotube structure in the flexible carbon nanotube composite structure. When the structure of the carbon nanotubes is completely covered by the base material, the carbon nanotubes can be further separated into the Nylon carbon nanotube composite knots by cutting or the like to ensure the electrode 206 and The carbon nanotube structure is electrically connected. It can be understood that two electrodes can be pre-formed to be electrically connected to the carbon nanotube structure, and 201039678 is further configured to form a composite structure of a nano-carbon composite with a flexible matrix material. Referring to Fig. 2, a second embodiment of the present invention provides a line heat source 3, which includes a heating element 3〇4 and two electrodes spaced apart and electrically connected to the heating element 3〇4. The heating element 3〇4 comprises a linear carbon nanotube composite structure. The linear carbon nanotube composite structure is the same as the linear carbon nanotube composite structure in the first embodiment of the present invention. The linear carbon nanotube composite structure comprises at least one carbon nanotube structure and a new frequency, and the recorded refractory is less than one carbon nanotube pipeline. The nanocarbon line-like structure comprises a plurality of micropores, and the matrix material is prepared for the micro-carbon pipeline. The linear carbon nanotube composite knot may comprise a matrix and at least a nanocarbon filament structure composited in the matrix. It can be understood that 'the nano carbon line-like structure is directly placed in the mold, and then the liquid sorrow 13⁄4 molecular material is injected into the liquid-phase nano-carbon line structure, and finally the heat is solidified to prepare the linear nai. Meter broken tube composite structure. The naphtha carbon nanotube heterostructure and the matrix (4) are the same as the nano-barrier structure and the matrix material of the present invention. Due to the self-supporting nature of the nanocarbon line-like structure, the linear carbon nanotube composite structure also has self-supporting property. The electrode 302 may surround the surface of the linear carbon nanotube composite and be electrically connected to the nanocarbon line-like structure. The material of the electrode 302 is the same as that of the electrode 206 in the first embodiment of the present invention. The line secret and the preparation method thereof have the following m, since the nano tube-breaking structure is - self-supporting structure and the carbon nanotubes are distributed in the neat tube structure, the shape is 42 201039678 ο 〇 distribution, the self-supporting The carbon nanotube structure is directly combined with the matrix material, so that the carbon nanotubes in the heating element formed after the composite are still combined with each other to maintain the shape of a carbon nanotube structure, so that the carbon nanotubes in the heating element are uniform. The distribution forms a conductive network, which is not limited by the concentration of the carbon nanotubes in the solution, so that the mass percentage of the carbon nanotubes in the heating element can reach 99%, so that the heat source has higher heating performance. The surface of the 'silk body (4) is not limited to a polymer, making the application range of the heat source wider. Second, because the carbon nanotubes have better strength and toughness, the carbon nanotube structure has a higher strength, which is better, and is not easily broken, so that it has a long service life. Special, when the nanocarbon When the tube structure is combined with the flexible matrix material to form a heating element, a flexible heat source can be prepared, which makes the heat source have a wider application range. Third, the carbon nanotubes in the carbon nanotube structure are evenly distributed, so the heating element has the thickness of the uniform sentence and the heat of the remainder. Since the nano-carbon surface electrothermal conversion efficiency is high, the line _ has the characteristics of rapid temperature rise, small m after length, fast heat exchange rate, and jurisdictional efficiency gate. Fourth, the smaller the carbon nanotubes make the carbon nanotube structure have a smaller thickness, and a microwire heat source can be prepared for heating the micro device. ^五' When the carbon nanotube structure includes the carbon nanotube pull-off, the carbon nanotubes in the carbon nanotube film are arranged along the same direction in the same direction, and have good electrical conductivity, so that the good touch can. Sixth, the Qingcheng self-supporting _ silk carbon tube structure, ~4 shot structure and the base material directly combined to form a heating element method ^ ^ ^ tube in the heating element (four) content can be square (four) _. And the base material, paste plum carbon 43 201039678 In summary, the invention has indeed met the requirements of the invention patent, and the patent application is filed according to law. However, the above description is only a preferred embodiment of the present invention, and it is not possible to limit the application of the case to the full application. Any equivalent modification made by those who are familiar with this New Art in accordance with the spirit of the present invention should cover the scope of the application. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic structural view of a line heat source according to a first embodiment of the present invention. 2 is a cross-sectional view of the line heat source of FIG. 1 taken along line 1141. 3 is a schematic cross-sectional view of the line heat source of FIG. 2 taken along the line dish. Fig. 4 is a schematic view showing a line heat source comprising a layered carbon nanotube composite structure disposed on a linear lancet structure according to a first embodiment of the present invention, wherein the towel base material is infiltrated into the carbon nanotube structure. Fig. 5 is a schematic view showing a line heat source according to a first embodiment of the present invention comprising a layered nanotube composite structure disposed on a surface of a linear support structure, wherein the carbon nanotube structure is reinforced in the base material. σ ' Fig. 6 is a schematic view showing the line heat source of the first embodiment of the present invention comprising a single linear carbon nanotube composite structure disposed on the surface of the linear support structure. Fig. 7 is a schematic view showing a line heat source according to a first embodiment of the present invention comprising a plurality of linear carbon nanotube composite structures disposed on a surface of a linear branch structure. Fig. 8 is a scanning electron micrograph of a structure of a carbon nanotube makeup film in a line heat source according to a first embodiment of the present invention. Fig. 9 is a schematic view showing the structure of the carbon nanotube segments in the carbon nanotube film structure of Fig. 8. 44 201039678 Figure ί is a scanning electron micrograph of the arrangement of the carbon nanotubes in the nano-carbon tube barrier film structure in the first direction of the present invention. Fig. 11 is a scanning electron micrograph of the arrangement of the carbon nanotubes in the fine-grained, carbon nanotube-rolled film structure in the fourth embodiment of the present invention. Figure 12 is a scanning electron micrograph of the structure of a carbon nanotube flocculation membrane in a line heat source of the crucible-example of the present invention. Figure 13 is a scanning electron micrograph of a non-twisted nanocarbon line in a line heat source according to a first embodiment of the present invention. Figure 扫描 is a scanning electron micrograph of the nano carbon line of the first implementation of the invention. Fig. 15 is a sectional scanning electron micrograph of a composite structure of a carbon nanotube film and an epoxy resin in a line heat source according to a first embodiment of the present invention. Figure 16 is a flow chart showing a method of preparing a line heat source according to a first embodiment of the present invention. Figure 17 is a photograph of a floc structure of a carboniferous tube of a line heat source according to an embodiment of the present invention. Fig. 18 is a flow chart showing a method of recombining a carbon nanotube structure provided on the surface of a linear support structure with a polymer material according to a first embodiment of the present invention. Fig. 19 is a flow chart showing another method of preparing a line heat source according to the first embodiment of the present invention. 20 is a structural diagram of a line heat source according to a second embodiment of the present invention. [Main component symbol description] Carbon nanotube segment 143 Carbon nanotube 145 45 201039678 'Line heat source 20,30 Linear support structure 202 Heating element 204, 304 Electrode 206, 302 Insulation protective layer 208 Heat reflective layer 210 Base material 2042 Nano Carbon tube structure 2044 0 base body 2040 〇46

Claims (1)

201039678 ' 七、申請專利範圍: 1. 一種線熱源,其改良在於,其包括: 一線狀支撐結構; 加熱元件δ又置於線狀支撐結構的表面;以及 兩個電極,該兩個電極間隔設置且與該加熱元件電連接; 所述加熱元件包括至少-奈米碳管複合結構,該奈米碳管複合 結構包括-基體及-奈米碳管聽構複合機基體巾,且該奈 〇 米碳管膜結構包括沿—固定方向或不同方向擇優取向排列的 多個奈米碳管。 2_如申請專利範圍第1項所述的線熱源,其中,所述奈米碳管膜 結構中的奈米碳管與奈米碳管膜結構的表面成—夾角卜其 中’ β大於等於〇度且小於等於15度。 3. 如申請專利範圍帛1項所述的線熱源,其中,所述奈米碳管膜 、、’σ構中的奈米碳管部分交疊,並通過凡德瓦爾力相互吸引,緊 〇 密結合。 4. 如申請專利範圍第1項所述的線熱源,其中,所述奈米碳管膜 結構的厚度為1微米〜1毫米。 如申π專利範圍第4項所述的線熱源,其中,所述奈米碳管膜 ”'籌的早位面積熱容小於2x10 4焦耳每平方楚米開爾文。 .如申睛專利範圍第4項所述的線熱源,其中,所述奈米碳管膜 結構的單位面積熱容小於或等於1.7xl0_6焦耳每平方釐米開爾 文。 47 201039678 7· 專利範圍第1項所述的線熱源’其中,所述至少一奈米 碳官複合結構纏繞或包覆於所述線狀支撐結構的表面。 8.如申物_第!項所述的線_,其中,所述基體完全包 覆該奈米碳管獏結構。 9·如1請專利範圍第!項所述的線熱源,其中,所述基體至少部 分嵌入該奈米碳管獏結構中。 10. 如帽專利範圍第!項所述的線熱源,其中,所述基體材料包 Ο 括高分子材料以及無機非金屬材料中的一種或多種。 11. 如申請專利翻第i項所述的線熱源,其中,所述兩個電極分 別與所述奈米碳管膜結構電連接。 12. 如申請專利範圍第1項所述的線熱源,其中,所述線熱源進-步包括一熱反射層。 13. 如申請專利範圍第12項所述的線熱源,其十,所述熱反射層 的材料為金屬氧化物、金屬鹽及陶瓷中的一種或多種。 Ο Μ.如申請專利範圍第12項所述的線熱源,其中,所述熱反射層 的厚度為100微米〜0.5毫米。 15. 如申請專利範圍第1項所述的線熱源,其中,所述線熱源進一 步包括一絕緣保護層設置;^加熱元件表面。 16. 如申請專利範圍第15項所述的線熱源,其中,所述絕緣保護 層的材料為橡膠及樹脂中的一種或多種。 17·如申請專利範圍第15項所述的線熱源,其中,所述絕緣保護 層的厚度為0.5毫米〜2毫米。 48 201039678 - 18. —種線熱源,其改良在於,其包括: 一線狀支撐結構; 一加熱元件設置於線狀支撐結構的表面;以及 兩個電極,該兩個電極間隔設置且與該加熱元件電連接, 所述加熱元件包括至少一奈米碳管複合結構,所述奈米碳管複 合結構包括-奈米碳管膜結構以及基體材料,該奈米碳管膜結 構包括沿-©定方向或不同方向擇優取向制的多個奈米碳 〇 管,所述基體材料複合於該奈米碳管膜結構中。 19. 如申請專利範圍第18項所述的線熱源,其中,所述奈米碳管 膜結構具有多個微孔,所述基體材料渗透於該奈米碳管膜結構 的微孔中。 20. 如申請專利範圍第19項所述的線熱源,其中,所述微孔孔徑 小於10微米。 21. —種線熱源,其改良在於,其包括: 0 —線狀支撐内芯; 一加熱元件環繞包覆該線狀讀内芯,所述加熱元件包括至少 -奈米碳管複合結構,該奈米碳管複合結構包括—基體及一與 之複合的奈米碳管赌構,該絲碳管麟構包括沿—固定方 向或不同方向擇優取向排列的多個奈米碳管; 兩個電極’該兩個電極間隔設置且與該加熱元件電連接,·以及 -絕緣保護層包覆該加熱元件於其内。 49201039678 ' VII. Patent application scope: 1. A line heat source, the improvement thereof comprises: a linear support structure; the heating element δ is placed on the surface of the linear support structure; and two electrodes, the two electrodes are arranged at intervals And electrically connected to the heating element; the heating element comprises at least a carbon nanotube composite structure, the carbon nanotube composite structure comprises a substrate and a carbon nanotube organic composite substrate towel, and the naphtha The carbon tubular membrane structure includes a plurality of carbon nanotubes arranged in a preferred orientation along a fixed direction or in different directions. 2) The line heat source according to claim 1, wherein the carbon nanotube membrane structure and the surface of the carbon nanotube membrane structure are at an angle of -β is greater than or equal to 〇 Degree is less than or equal to 15 degrees. 3. The linear heat source as claimed in claim 1, wherein the carbon nanotube film, the carbon nanotubes in the 'sigma structure partially overlap, and are attracted to each other by Van der Waals force, close to each other Close combination. 4. The line heat source according to claim 1, wherein the carbon nanotube film structure has a thickness of from 1 μm to 1 mm. The linear heat source according to claim 4, wherein the carbon nanotube film has a heat capacity of less than 2 x 10 4 joules per square Chum Kelvin. The linear heat source according to the item, wherein the carbon nanotube membrane structure has a heat capacity per unit area less than or equal to 1.7 x 10 6 joules per square centimeter Kelvin. 47 201039678 7 · The line heat source described in the first item of the patent range ' The at least one nano carbon-composite structure is wound or coated on the surface of the linear support structure. 8. The wire according to the item of claim _, wherein the substrate completely covers the nano The carbon heat source structure of the present invention, wherein the base body is at least partially embedded in the carbon nanotube structure, as described in the patent scope of the present invention. The line heat source, wherein the base material comprises one or more of a polymer material and an inorganic non-metal material. 11. The line heat source according to claim i, wherein the two electrodes are respectively The carbon nanotube membrane structure is electrically connected. The line heat source according to claim 1, wherein the line heat source further comprises a heat reflecting layer. 13. The line heat source according to claim 12, wherein the heat is The material of the reflective layer is one or more of a metal oxide, a metal salt, and a ceramic. The wire heat source according to claim 12, wherein the heat reflective layer has a thickness of 100 μm to 0.5 mm. 15. The line heat source of claim 1, wherein the line heat source further comprises an insulating protective layer disposed; the heating element surface. 16. The line heat source according to claim 15 of the patent application, The material of the insulating protective layer is one or more of a rubber and a resin. The wire heat source according to claim 15, wherein the insulating protective layer has a thickness of 0.5 mm to 2 mm. 48 201039678 - 18. - Line heat source, the improvement comprising: a linear support structure; a heating element disposed on a surface of the linear support structure; and two electrodes spaced apart from each other The element is electrically connected, the heating element comprises at least one carbon nanotube composite structure, the nano carbon tube composite structure comprises a carbon nanotube membrane structure and a matrix material, and the carbon nanotube membrane structure comprises a a plurality of carbon nanotubes of a preferred orientation, or a direction of a different orientation, wherein the matrix material is composited in the carbon nanotube membrane structure. The carbon nanotube membrane structure has a plurality of micropores, and the matrix material is infiltrated into the micropores of the carbon nanotube membrane structure. The linear heat source according to claim 19, wherein the micro The pore size is less than 10 microns. 21. A seed line heat source, the improvement comprising: 0 - a linear support inner core; a heating element surrounding the linear read inner core, the heating element comprising at least a carbon nanotube composite structure, The carbon nanotube composite structure comprises a substrate and a carbon nanotube composite structure, the carbon nanotube structure comprising a plurality of carbon nanotubes arranged in a preferred orientation along a fixed direction or in different directions; two electrodes The two electrodes are spaced apart and electrically connected to the heating element, and an insulating protective layer encloses the heating element therein. 49
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