TW201925558A - Method of fabricating carbon fiber composite with biomass feedstock transformed - Google Patents

Method of fabricating carbon fiber composite with biomass feedstock transformed Download PDF

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TW201925558A
TW201925558A TW106142387A TW106142387A TW201925558A TW 201925558 A TW201925558 A TW 201925558A TW 106142387 A TW106142387 A TW 106142387A TW 106142387 A TW106142387 A TW 106142387A TW 201925558 A TW201925558 A TW 201925558A
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lignin
raw material
carbon fiber
fiber
composite
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TW106142387A
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TWI643988B (en
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許銘軒
陳文華
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行政院原子能委員會核能研究所
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Abstract

The present invention uses biomass feedstock to produce carbon fiber composite with low cost. A method is provided to fabricate the carbon fiber composite through transforming waste of fibrous biomass. Therein, degradation of lignin-based carbon fiber does not happen easily; surface unevenness of the fiber is improved; and solvent used during procedure can be recycled. Thus, the operating cost for fabricating carbon fiber is reduced. The present invention is characterized in that a special ionic liquid is used to uniformly dissolve the feedstock. A wet-spinning apparatus is used for coordination on fabricating a lignin/standard cellulose biomass fiber composite. The Ionic solvent can be recycled for reuse. Furthermore, by mixing the biomass feedstock with the Ionic solvent, the structural defects of the lignin-based carbon fiber can be improved for preventing from being broken easily. A pre-treatment of soaking with a phenolic resin is used for stabilizing the lignin-based carbon fiber. The shrinkage during carbonizing the lignin-based carbon fiber is significantly reduced with the phenomenon of brittle fracture reduced as well. Through two stages of heating, the glass transition temperature is enhanced for preserving the form of fiber through maintaining the surface integrity of the lignin-based fiber. The lignin/standard cellulose biomass fiber composite thus obtained has a uniform, integrated and non-porous surface. A stable and low-cost system for continuously producing carbon fiber composite from biomass is established.

Description

利用生質原料轉化生質複合碳纖維之方法Method for converting raw material composite carbon fiber by using raw material

本發明係有關於一種利用生質原料轉化生質複合碳纖維之方法,尤指針對廣泛纖維生質原料提供一種適用於生質廢棄物轉化生質複合碳纖維,特別係指改善木質素基碳纖維易降解與表面不均之現象以及製程溶劑不可回收之特性,有效降低碳纖維製程操作成本者。The invention relates to a method for converting raw carbon composite carbon fiber by using raw material, in particular to provide a composite carbon fiber suitable for conversion of raw biomass to raw fiber raw materials, in particular to improve the degradation of lignin-based carbon fiber. The phenomenon of uneven surface and the non-recyclable nature of the process solvent can effectively reduce the operating cost of the carbon fiber process.

碳纖維(Carbon fiber)含碳量大於90%,化學結構近似石墨並具備皆高拉伸強度、高彈性模數、高導電性及高導熱率等優異性能,在相同體積下重量為鋼的三分之一,強度卻可達四倍之高,廣泛應用於航太、軍事、能源及運動等材料研發領域。現行製備碳纖維之前趨材料主要為縲縈(Rayon)、聚丙烯腈(Polyacrylonitrile, PAN)以及瀝青(Pitch)。其中縲縈為最早被製備為高強度碳纖維之原料,但受限於產率低及聚丙烯腈材料之竄起,迅速取代並成為碳纖維工業主要製程,之後瀝青原料雖有成本上之優勢但論及碳纖維性能與產量仍不及聚丙烯腈材料,目前聚丙烯腈已廣泛應用於商業發展,市面上80%之商業碳纖維係由聚丙烯腈製作而得,碳纖維製造過程普遍經過預氧化、低溫碳化及高溫碳化(石墨化)等熱處理及熱解程序,但在氧化纖維集中放熱過程及高溫縮合之程序容易發生物理緻密特性低及結構缺陷等非均質破碎現象,此外上述皆為石化原料,係以石油基或煤基等不可再生資源為前趨材料,各別存在聚丙烯腈碳纖維碳化緩慢、價格昂貴以及瀝青碳纖維質量分布不均之情況,受限於前趨材料資源漸漸匱乏及碳纖維需求量增加,造成碳纖維成本日益攀升,因此可再生非石油基之低成本碳纖材料開發為現今研究重點。 纖維原料結構由纖維素、半纖維素及木質素組成,木質素屬非晶體之高分子化合物,主要為芳香族聚合而成,其基本結構為苯丙烷(C6~C8)型之結構,在一般草本植物約占15~20%,木本植物則可達30% ,而木質素之組成富含60%以上之碳成分可作為碳之前趨替代材料,加上木質素屬於可再生資源與聚丙烯腈及瀝青相較之下,預期成本相對降低,凸顯木質素之高潛在應用價值。 目前以木質素基碳纖維為生質基碳纖維技術中較具有發展突破之空間,如木質素或木質素衍生物之自由羥基可被單價及雙價自由基衍生化,使其具備可紡性紡絲成為纖維,再透過一般穩定化流程形成非熱塑性之安定纖維即可碳化成碳纖維。木質素在未改性之情況並非良好纖維成型之材料,多數文獻係添加額外添加劑促使進行衍生化作用並透過熔融紡絲形成長纖維,然而添加劑對於以木質素原料為基礎之紡絲纖維安定性及後續碳化過程易造成不利影響,如J.F.Kadla等人所提文獻(J.F. Kadla, S Kubo, R.A. Venditti, R.D. Gilbert, A.L. Compere, W Griffith. Lignin-based carbon fibers for composite fiber applications Carbon, 2002, Vol.40 (15), pp.2913-2920)採用硫酸鹽木質素添加5%比例聚環氧乙烷(Polyethylene oxide, PEO)進行熔融紡絲,固化過程長纖維具備高度黏性且碳化之碳纖維只具備0.4Gpa拉伸強度,彈性模量介於40~50GPa範圍內,遠低於市售碳纖維數值甚至低於玻璃纖維屬性,且PEO屬於合成高分子,常溫下具備易燃、致癌及刺激性特性,用於室溫紡絲製程仍存在安全疑慮;此外,茵芬提亞公司於中華民國專利案TW201335452提出一種藉由不存在氧化劑之情況下熱處理,自軟木鹼性木質素製造穩定之木質素纖維的方法,係以不存在氧化劑方式透過不同升溫速率變化進行穩定熱處理,藉由一般鹼性溶液所得黑液進行萃取木質素,雖有助於維持表面完整性,但此法操作上需要大量鹼性溶劑且不具回收性。另外,史託拉安索公司亦提出中華民國專利案TW201715106,係於沉澱浴中加入某些鹽而使木質素之損失最小化,但其木質素在製備碳纖維過程中穩定性較差。 目前多數專利著重開發再生資源之木質素基碳纖維熱塑性製程改良,需要添加衍生物達到熱塑性目的,如WO2012156441A1係利用N-甲基嗎啉-N-氧化物(N-methylmorpholine-N-oxide, NMMO)溶劑使木質素纖維溶解,但此法易造成木質素纖維在成形槽中降解損耗且不可回收 。故,ㄧ般習用者於熔融紡絲加工過程容易造成木質素降解,係無法符合使用者於實際使用時之所需。Carbon fiber has a carbon content of more than 90%, a chemical structure similar to graphite, and has excellent tensile strength, high modulus of elasticity, high electrical conductivity and high thermal conductivity. The weight of the steel is three cents under the same volume. One of them, the strength is up to four times higher, and is widely used in the research and development of materials such as aerospace, military, energy and sports. The current preparation of carbon fiber precursor materials are mainly Rayon, Polyacrylonitrile (PAN) and Pitch. Among them, 缧萦 was the first material to be prepared as high-strength carbon fiber, but it was limited by the low yield and the rise of polyacrylonitrile material, which quickly replaced and became the main process of the carbon fiber industry. After that, although the asphalt raw material has the advantage of cost, And the performance and yield of carbon fiber is still less than that of polyacrylonitrile. At present, polyacrylonitrile has been widely used in commercial development. 80% of the commercial carbon fiber on the market is made of polyacrylonitrile. The carbon fiber manufacturing process is generally pre-oxidized and low-temperature carbonized. Heat treatment and pyrolysis procedures such as high temperature carbonization (graphitization), but the process of exothermic process and high temperature condensation of oxidized fibers is prone to heterogeneous fracture phenomena such as low physical density and structural defects, and the above are all petrochemical raw materials, which are petroleum. The non-renewable resources such as base or coal are predecessor materials, and the slow carbonization of polyacrylonitrile carbon fiber, the high price and the uneven distribution of asphalt carbon fiber quality are limited by the gradual shortage of material resources and the increase of carbon fiber demand. Reducing the cost of carbon fiber, so it can regenerate non-petroleum-based low-cost carbon fiber Develop research priorities for today. The fiber raw material structure is composed of cellulose, hemicellulose and lignin. The lignin is an amorphous polymer compound, which is mainly composed of aromatic polymerization. Its basic structure is phenylpropane (C6-C8) type structure. Herbs account for about 15-20%, woody plants can reach 30%, and lignin composition is rich in more than 60% of carbon components can be used as a carbon replacement material, plus lignin belongs to renewable resources and polypropylene. Compared with nitrile and asphalt, the expected cost is relatively low, highlighting the high potential application value of lignin. At present, lignin-based carbon fiber is a breakthrough in the development of bio-based carbon fiber technology. For example, the free hydroxyl group of lignin or lignin derivative can be derivatized by monovalent and bivalent free radicals to make it spinnable. The fibers are carbonized and then carbonized into carbon fibers by forming a non-thermoplastic stabilizer fiber through a general stabilization process. Lignin is not a good fiber-forming material in the unmodified case. Most of the literature adds additional additives to promote derivatization and melt-spinning to form long fibers. However, the additive is suitable for spinning fiber based on lignin raw materials. And subsequent carbonization processes are prone to adverse effects, such as JF Kadla, S Kubo, RA Venditti, RD Gilbert, AL Compere, W Griffith. Lignin-based carbon fibers for composite fiber applications Carbon, 2002, Vol .40 (15), pp.2913-2920) melt-spinning with sulphated lignin added with 5% ratio of polyethylene oxide (PEO). The long fibers in the curing process are highly viscous and carbonized carbon fibers only With 0.4Gpa tensile strength, the elastic modulus is in the range of 40-50 GPa, far lower than the commercial carbon fiber value or even lower than the fiberglass property, and PEO is a synthetic polymer with flammable, carcinogenic and irritating properties at room temperature. There are still safety concerns for the room temperature spinning process; in addition, Inventia Company proposed a case in the Republic of China patent case TW201335452 Heat treatment in the absence of an oxidizing agent, a method for producing a stable lignin fiber from softwood alkaline lignin, which is subjected to a stable heat treatment in the absence of an oxidizing agent through a different heating rate change, and is obtained by extracting black liquor obtained from a general alkaline solution. Quality, while helping to maintain surface integrity, requires a large amount of alkaline solvent and is not recyclable. In addition, Stora Enso also proposed the Republic of China patent case TW201715106, which added some salts in the precipitation bath to minimize the loss of lignin, but its lignin has poor stability in the preparation of carbon fiber. At present, most of the patents focus on the development of renewable materials, lignin-based carbon fiber thermoplastic process improvement, the need to add derivatives for thermoplastic purposes, such as WO2012156441A1 using N-methylmorpholine-N-oxide (NMMO) The solvent dissolves the lignin fiber, but this method easily causes degradation of the lignin fiber in the forming tank and is not recyclable. Therefore, it is easy for the acne-like user to cause lignin degradation during the melt spinning process, which cannot meet the needs of the user in actual use.

本發明之主要目的係在於,克服習知技藝所遭遇之上述問題並針對廣泛纖維生質原料提供一種適用於生質廢棄物轉化生質複合碳纖維,本製程篩選合適且可回收利用之離子溶液作為紡絲溶劑溶解木質素/標準纖維素混合物,並採用連續濕式紡絲設備製備木質素/標準纖維素生質複合纖維,再進一步以熱處理碳化為木質素/標準纖維素生質複合碳纖維,透過生質原料混摻方式大幅改善原有熔融紡絲製程木質素易降解與表面不均之現象以及製程溶劑不可回收之特性,有效降低碳纖維製程操作成本,並提升木質素/標準纖維素生質複合碳纖維基本物理性質,展現顯著差異性之利用生質原料轉化生質複合碳纖維之方法。 為達以上之目的,本發明係一種利用生質原料轉化生質複合碳纖維之方法,其至少包含下列步驟:溶解生質原料程序:將生質原料利用溶劑分離出90%以上固體木質素微粒,將該木質素微粒與標準纖維素混摻後加入特殊離子液體混合攪拌使木質素/標準纖維素混合物均勻分散溶解,配製成1~15 wt%紡絲溶液,並配合濕式紡絲設備紡製木質素/標準纖維素生質複合纖維,過程中移除之離子液體可加以回收重新作為紡絲溶劑使用;穩定化/預氧化程序:利用酚醛樹脂預浸泡該木質素/標準纖維素生質複合纖維,再置於高通氧環境進行穩定化及預氧化,使結構產生縮合反應,轉為環狀穩定結構維持複合纖維表面完整性,獲得木質素/標準纖維素生質複合氧化纖維;以及碳化程序:係將該木質素/標準纖維素生質複合氧化纖維置放於惰性氣氛之高溫環境內,以兩階段加熱進行碳化,藉由熱處理碳化消除不純物及雜質,製得木質素/標準纖維素生質複合碳纖維。 於本發明上述實施例中,該溶解生質原料程序係將該木質素微粒與該離子液體混合配製成10~15 wt%溶液,在65~95°C下加熱4~6小時,置於水中成形進行溶解特性評估。 於本發明上述實施例中,該溶解生質原料程序中之木質素微粒與該標準纖維素係以5~10%比例混摻。 於本發明上述實施例中,該生質原料係選自稻稈、蔗渣、芒草、狼尾草、柳枝稷、玉米稈、木材及竹子之生質廢棄物。 於本發明上述實施例中,該離子液體與該木質素微粒具有表示其分子與木質素性質相互滲透能力之Hansen溶解參數。 於本發明上述實施例中,該離子液體係選自1-丁基-3-甲基咪唑氯(1-Butyl-3-Methylimidazolium Chloride, [BMIM]Cl)、1-丁基-3-甲基咪唑六氟磷酸鹽(1-Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6)、1-丁基-3-甲基咪唑四氟溴酸 (1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM]BF4)、或其他溶解參數與木質素性質相近之離子液體。 於本發明上述實施例中,該穩定化/預氧化程序係將該木質素/標準纖維素生質複合纖維與該酚醛樹酯於凝固浴浸泡24小時後放置於氧化爐,以預氧化溫度150~300°C、升溫速率0.5~3°C/min、及持溫時間0~2小時進行穩定化及預氧化。 於本發明上述實施例中,該碳化程序係將該木質素/標準纖維素生質複合氧化纖維置放於氮氣氣氛(>99.99%)之高溫爐內,以升溫速率170~200°C/h加熱至800~900°C,並於1200~1400°C溫度下完成碳化過程。The main object of the present invention is to overcome the above problems encountered in the prior art and to provide a composite carbon fiber suitable for conversion of raw biomass to raw fiber raw materials for a wide range of fiber raw materials, and to select an appropriate and recyclable ionic solution for the process. The spinning solvent dissolves the lignin/standard cellulose mixture, and the lignin/standard cellulose raw composite fiber is prepared by continuous wet spinning equipment, and further carbonized into lignin/standard cellulose raw composite carbon fiber through heat treatment. The raw material mixing method greatly improves the phenomenon of easy degradation and surface unevenness of the original melt spinning process, and the non-recyclable nature of the process solvent, effectively reducing the operating cost of the carbon fiber process, and improving the lignin/standard cellulose biocomposite compound. The basic physical properties of carbon fiber, showing a significant difference in the method of converting raw biomass composite carbon fiber using raw materials. For the purpose of the above, the present invention is a method for converting a raw material composite carbon fiber by using a raw material, which comprises at least the following steps: a procedure for dissolving the raw material: separating the raw material into more than 90% of the solid lignin particles by using a solvent. Mixing the lignin particles with standard cellulose, adding special ionic liquid, mixing and stirring, dispersing and dissolving the lignin/standard cellulose mixture uniformly, preparing into a spinning solution of 1-15 wt%, and spinning with wet spinning equipment. Lignin/standard cellulose raw composite fiber, the ionic liquid removed in the process can be recycled and reused as a spinning solvent; Stabilization/preoxidation procedure: pre-soaking the lignin/standard cellulose raw material with phenolic resin The composite fiber is further stabilized and pre-oxidized in a high-pass oxygen environment to cause a condensation reaction of the structure, and the ring-shaped stable structure is maintained to maintain the surface integrity of the composite fiber, and the lignin/standard cellulose raw composite oxidized fiber is obtained; and carbonization is obtained. Procedure: The lignin/standard cellulose biocomposite oxidized fiber is placed in a high temperature environment of an inert atmosphere, and added in two stages. The carbonization is carried out by heat, and the impurities and impurities are removed by heat treatment to obtain lignin/standard cellulose raw composite carbon fiber. In the above embodiment of the present invention, the dissolved raw material raw material is prepared by mixing the lignin microparticles with the ionic liquid to prepare a 10-15 wt% solution, and heating at 65 to 95 ° C for 4 to 6 hours, and placing Forming in water for evaluation of dissolution characteristics. In the above embodiment of the present invention, the lignin microparticles in the dissolved raw material raw material program are blended with the standard cellulose system in a ratio of 5 to 10%. In the above embodiment of the present invention, the raw material is selected from the group consisting of rice straw, bagasse, Miscanthus, Pennisetum, switchgrass, corn stalk, wood and bamboo. In the above embodiment of the invention, the ionic liquid and the lignin microparticles have Hansen dissolution parameters indicative of their ability to interpenetrate with their lignin properties. In the above embodiment of the invention, the ionic liquid system is selected from the group consisting of 1-Butyl-3-Methylimidazolium Chloride (BMIM]Cl), 1-butyl-3-methyl 1-Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6, 1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM]BF4 Or other ionic liquids whose solubility parameters are similar to those of lignin. In the above embodiment of the present invention, the stabilization/preoxidation procedure is performed by immersing the lignin/standard cellulose raw composite fiber and the phenolic resin in a coagulation bath for 24 hours, and then placing it in an oxidation furnace at a pre-oxidation temperature of 150. Stabilization and pre-oxidation were carried out at -300 ° C, a heating rate of 0.5 to 3 ° C / min, and a holding time of 0 to 2 hours. In the above embodiment of the present invention, the carbonization process is to place the lignin/standard cellulose bio-composite oxidized fiber in a high-temperature furnace of a nitrogen atmosphere (>99.99%) at a heating rate of 170 to 200 ° C / h. It is heated to 800-900 ° C and the carbonization process is completed at a temperature of 1200-1400 ° C.

請參閱『第1圖~第4圖』,係分別為本發明之流程架構示意圖、本發明之木質素/標準纖維素生質複合纖維表面型態圖、本發明之木質素/標準纖維素生質複合氧化纖維照片圖、及本發明之木質素/標準纖維素生質複合碳纖維表面及截面型態圖。如圖所示:本發明係建立一種利用生質原料轉化生質複合碳纖維之方法,主要實施架構如第1圖所示,其至少包含下列步驟: 溶解生質原料程序s11:選用生質原料1可為稻稈、蔗渣、芒草、狼尾草、柳枝稷、玉米稈、木材及竹子等任何常見生質廢棄物,經溶劑2分離90%以上固體木質素微粒3,將該木質素微粒3與標準纖維素4混摻後加入特殊離子液體5混合攪拌使木質素/標準纖維素混合物均勻分散溶解,配製成1~15 wt%紡絲溶液,透過濕式紡絲設備紡製木質素/標準纖維素生質複合纖維6,過程中移除之離子液體5可經由系統回收重新作為紡絲溶劑使用。其中,本發明之特點在於採用之離子液體係透過Hansen溶解理論進行分子與木質素性質相近之離子液體所設計,藉此提高其二者互溶性。所使用之離子液體可為1-丁基-3-甲基咪唑氯(1-Butyl-3-Methylimidazolium Chloride, [BMIM]Cl)、1-丁基-3-甲基咪唑六氟磷酸鹽(1-Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6)、1-丁基-3-甲基咪唑四氟溴酸 (1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM]BF4)、或其他溶解參數與木質素性質相近之離子液體,溶解過程係將木質素微粒與離子液體混合配製成10~15 wt%溶液,在65~95°C下加熱4~6小時,置於水中成形進行溶解特性評估。另外本發明係應用一般習知濕式紡絲技術製備木質素/標準纖維素生質複合纖維,操作方式即是將木質素微粒/離子液體此黏性溶液送入注射幫浦,經由推送控制流出速度形成線狀溶液,通過空氣間隙(air gap)幫助分子溶液進行順向排列,而進入成形槽後,離子液體替換為木質素之非溶劑,如:水,待木質素纖維成形後以螺桿牽引施予纖維張力並可調整纖維細度及伸率。 穩定化/預氧化程序s12:進行穩定化前,將該木質素/標準纖維素生質複合纖維6與酚醛樹脂7於凝固浴浸泡24小時後放置於高通氧環境,木質素/標準纖維素生質複合纖維預氧化溫度(主要依據DSC與TGA設定溫度)150~300°C、升溫速率0.5~3°C/min、及持溫時間0~2小時進行穩定化及預氧化,此時結構產生縮合反應,轉為環狀穩定結構維持複合纖維表面完整性,獲得木質素/標準纖維素生質複合氧化纖維8。 碳化程序s13:係將該木質素/標準纖維素生質複合氧化纖維8置放於惰性氣氛之高溫環境內,以兩階段加熱進行碳化,藉由升溫速率170~200°C/h加熱至800~900°C,並於1200~1400°C溫度下完成碳化過程,利用熱處理碳化消除不純物及雜質,製得木質素/標準纖維素生質複合碳纖維9。其中,本發明木質素纖維穩定化階段係利用酚醛樹脂預浸泡能夠大幅減少木質素纖維碳化期間引起收縮導致脆化斷裂之現象,並透過兩階段加熱提升玻璃轉移溫度,維持木質素纖維表面完整性保留纖維形式。如是,藉由上述揭露之流程構成一全新之利用生質原料轉化生質複合碳纖維之方法。 本發明係針對廣泛纖維生質原料提供一種適用於生質廢棄物轉化生質複合碳纖維,改善木質素基碳纖維易降解與表面不均之現象以及製程溶劑不可回收之特性,進而有效降低碳纖維製程操作成本。當運用時,本發明利用不同溶劑調和,施以不同反應溫度及反應時間一步兩相分離溶解原料中20~40%木質素,經減壓濃縮析出大於90%高純度、低損失量之木質素。於一具體實施例中,本發明篩選高木質纖維生質原料木片,經組成分析鑑定木片其纖維素含量 44.60%、半纖維素18.74%及木質素30.59%。前述木片之組成分析,係利用高效率液相層析儀(High-performance liquid chromatography, HPLC),使用Coregel-87H3 管柱,搭配流速1mL min-1 之4mM硫酸(H2 SO4 )沖提液於65°C進行樣品分離,透過折射率偵測器偵測化合物訊號並紀錄各化合物分離時間。依據混合溶劑將木片進行分相反應溶解木質素,經濃縮萃取液態溶液中純度大於90%之固體木質素微粒作為反應原料,將木質素微粒與離子液體進行溶解特性評估,表明此離子液體並未影響木質素微粒之基本性質,可單純作為溶解溶劑使用,紡絲前後木質素聚合度11.2 DPv,分子量1814。後續將固體木質素微粒與標準纖維素以5~10%比例混摻後加入離子液體,以80°C混合攪拌使混合物均勻分散溶解,配製1~10 wt%均質紡絲溶液,之後將紡絲液放入濕式紡絲設備,紡絲參數設定吐出量2.5 g/min、捲取速度10 m/min,即可獲得木質素/標準纖維素生質複合纖維,如第2圖所示。離子液體作為紡絲溶劑同時可於紡絲纖維製備完成加以回收重覆使用,即再以溶劑角色續溶解木質素及標準纖維素等反應物。預氧化階段則係將木質素/標準纖維素生質複合纖維預先浸泡防火酚醛樹脂24小時後放置氧化爐,穩定以2°C/min升溫至250°C並持溫1小時,可提高木質素/標準纖維素生質複合氧化纖維均勻度減少纖維間孔隙生成(纖維細度2.58±0.18、纖維伸度5.15±0.84、熱裂解溫度Please refer to FIG. 1 to FIG. 4 , which are schematic diagrams of the process architecture of the present invention, the surface morphology diagram of the lignin/standard cellulose raw composite fiber of the present invention, and the lignin/standard cellulose of the present invention. Photograph of the composite composite oxidized fiber, and the surface and cross-sectional pattern of the lignin/standard cellulose raw composite carbon fiber of the present invention. As shown in the figure: The present invention establishes a method for converting biomass composite carbon fiber by using raw material, and the main implementation structure is as shown in Fig. 1, which comprises at least the following steps: Dissolving raw material raw material program s11: selecting raw material 1 It can be any common biomass waste such as rice straw, bagasse, miscanthus, pennisetum, switchgrass, corn stalk, wood and bamboo. More than 90% of solid lignin particles 3 are separated by solvent 2. The lignin particles 3 and standard After the cellulose 4 is mixed, a special ionic liquid is added and mixed, and the lignin/standard cellulose mixture is uniformly dispersed and dissolved to prepare a spinning solution of 1 to 15 wt%, and the lignin/standard fiber is spun through the wet spinning device. The eucalyptus composite fiber 6, the ionic liquid 5 removed in the process can be reused as a spinning solvent via system recovery. Among them, the invention is characterized in that the ionic liquid system adopts the Hansen dissolution theory to design an ionic liquid having a similar molecular property to lignin, thereby improving the mutual solubility of the ionic liquid. The ionic liquid used may be 1-Butyl-3-Methylimidazolium Chloride ([BMIM]Cl), 1-butyl-3-methylimidazolium hexafluorophosphate (1) -Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6), 1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM]BF4, or other dissolution parameters and wood The ionic liquid with similar properties is prepared by mixing lignin microparticles with ionic liquid to prepare a 10-15 wt% solution, heating at 65-95 ° C for 4-6 hours, and forming in water to evaluate the solubility characteristics. In addition, the present invention uses a conventional wet spinning technique to prepare a lignin/standard cellulose raw composite fiber by operating the lignin/ionic liquid viscous solution into an injection pump and controlling the flow through the push. The velocity forms a linear solution, and helps the molecular solution to be aligned in the forward direction through the air gap. After entering the forming tank, the ionic liquid is replaced with a non-solvent of lignin, such as water, and the lignin fiber is shaped by a screw after being formed. The fiber tension is applied and the fiber fineness and elongation can be adjusted. Stabilization/preoxidation procedure s12: Before stabilizing, the lignin/standard cellulose bio-composite fiber 6 and the phenolic resin 7 are immersed in a coagulation bath for 24 hours, and then placed in a high-pass oxygen environment, lignin/standard cellulose raw Pre-oxidation temperature of the composite fiber (mainly based on DSC and TGA set temperature) 150 ~ 300 ° C, heating rate 0.5 ~ 3 ° C / min, and holding temperature for 0 ~ 2 hours for stabilization and pre-oxidation, the structure is produced The condensation reaction is converted into a cyclic stable structure to maintain the surface integrity of the composite fiber, and a lignin/standard cellulose bio-composite oxidized fiber 8 is obtained. Carbonization procedure s13: placing the lignin/standard cellulose raw composite oxidized fiber 8 in a high temperature environment of an inert atmosphere, carbonizing by two-stage heating, and heating to 800 by a heating rate of 170 to 200 ° C / h The carbonization process is completed at ~900 ° C and at a temperature of 1200 to 1400 ° C, and the impurities and impurities are removed by heat treatment to obtain lignin/standard cellulose raw composite carbon fiber 9 . Wherein, the stabilizing stage of the lignin fiber of the invention is pre-soaked with phenolic resin, which can greatly reduce the phenomenon of shrinkage caused by shrinkage during lignin fiber carbonization, and enhance the glass transition temperature through two-stage heating to maintain the surface integrity of the lignin fiber. Retain fiber form. As such, a novel process for converting biomass composite carbon fibers using raw materials is constructed by the above disclosed process. The invention provides a composite fiber carbon fiber suitable for conversion of raw biomass waste into raw fiber raw materials, improves the degradation of lignin-based carbon fiber and surface non-uniformity, and the non-recyclable characteristics of the process solvent, thereby effectively reducing the operation of the carbon fiber process. cost. When used, the invention utilizes different solvents to reconcile, applies different reaction temperatures and reaction time, and dissolves 20-40% lignin in the raw material by one-phase two-phase separation, and concentrates and precipitates more than 90% high purity and low loss lignin under reduced pressure. . In a specific embodiment, the present invention screens wood chips of high lignocellulosic raw materials, and the composition of the wood chips is 44.60%, hemicellulose 18.74% and lignin 30.59%. The composition analysis of the above wood chips was carried out by high-performance liquid chromatography (HPLC) using a Coregel-87H 3 column with 4 mM sulfuric acid (H 2 SO 4 ) at a flow rate of 1 mL min -1 . The sample was separated at 65 ° C, the compound signal was detected by a refractive index detector and the separation time of each compound was recorded. According to the mixed solvent, the wood chips are subjected to a phase separation reaction to dissolve the lignin, and the solid lignin particles having a purity greater than 90% in the liquid solution are concentrated and extracted as a reaction raw material, and the dissolution characteristics of the lignin particles and the ionic liquid are evaluated, indicating that the ionic liquid is not It affects the basic properties of lignin particles and can be used simply as a solvent. The degree of lignin polymerization before and after spinning is 11.2 DPv and the molecular weight is 1814. Subsequently, the solid lignin microparticles are mixed with standard cellulose in a ratio of 5-10%, and then added to the ionic liquid, and the mixture is uniformly dispersed and dissolved at 80 ° C to prepare a homogeneous spinning solution of 1 to 10 wt%, followed by spinning. The liquid is placed in a wet spinning apparatus, and the spinning parameter is set to a discharge amount of 2.5 g/min and a take-up speed of 10 m/min to obtain a lignin/standard cellulose raw composite fiber, as shown in Fig. 2. The ionic liquid can be used as a spinning solvent and can be recycled and reused after the preparation of the spun fiber, that is, the reactants such as lignin and standard cellulose are continuously dissolved in the solvent role. In the pre-oxidation stage, the lignin/standard cellulose raw fiber composite fiber is pre-soaked with the fireproof phenolic resin for 24 hours, and then placed in an oxidation furnace, and the temperature is raised to 250 ° C at 2 ° C / min and the temperature is maintained for 1 hour to increase the lignin. /Standard cellulosic composite oxidized fiber uniformity reduces interfiber pore formation (fiber fineness 2.58 ± 0.18, fiber elongation 5.15 ± 0.84, thermal cracking temperature

1‧‧‧生質原料 1‧‧‧ Raw materials

2‧‧‧溶劑 2‧‧‧Solvent

3‧‧‧木質素微粒 3‧‧‧Lignin particles

4‧‧‧標準纖維素 4‧‧‧Standard cellulose

5‧‧‧離子液體 5‧‧‧Ionic liquid

6‧‧‧木質素/標準纖維素生質複合纖維 6‧‧‧Lignin/Standard Cellulose Composite Fiber

7‧‧‧酚醛樹脂 7‧‧‧Phenolic resin

8‧‧‧木質素/標準纖維素生質複合氧化纖維 8‧‧‧Lignin/Standard Cellulose Biocomposite Oxidized Fiber

9‧‧‧木質素/標準纖維素生質複合碳纖維 9‧‧‧Lignin/Standard Cellulose Composite Carbon Fiber

s11‧‧‧溶解生質原料程序 S11‧‧‧Solid raw material raw material program

s12‧‧‧穩定化/預氧化程序 S12‧‧‧Stabilization/Preoxidation Procedure

s13‧‧‧碳化程序 S13‧‧‧carbonization procedure

第1圖,係本發明之流程架構示意圖。 第2圖,係本發明之木質素/標準纖維素生質複合纖維表面型態圖。 第3圖,係本發明之木質素/標準纖維素生質複合氧化纖維照片圖。 第4圖,係本發明之木質素/標準纖維素生質複合碳纖維表面及截面型態圖。Figure 1 is a schematic diagram of the process architecture of the present invention. Fig. 2 is a surface pattern diagram of the lignin/standard cellulose raw composite fiber of the present invention. Figure 3 is a photograph of the lignin/standard cellulose biocomposite oxidized fiber of the present invention. Figure 4 is a diagram showing the surface and cross-sectional morphology of the lignin/standard cellulose biocomposite carbon fiber of the present invention.

Claims (8)

一種利用生質原料轉化生質複合碳纖維之方法,其至少包含下列 步驟: 溶解生質原料程序:將生質原料利用溶劑分離出90%以上固體木質素微粒,將該木質素微粒與標準纖維素混摻後加入特殊離子液體混合攪拌使木質素/標準纖維素混合物均勻分散溶解,配製成1~15 wt%紡絲溶液,並配合濕式紡絲設備紡製木質素/標準纖維素生質複合纖維,過程中移除之離子液體可加以回收重新作為紡絲溶劑使用; 穩定化/預氧化程序:利用酚醛樹脂預浸泡該木質素/標準纖維素生質複合纖維,再置於高通氧環境進行穩定化及預氧化,使結構產生縮合反應,轉為環狀穩定結構維持複合纖維表面完整性,獲得木質素/標準纖維素生質複合氧化纖維;以及 碳化程序:係將該木質素/標準纖維素生質複合氧化纖維置放於惰性氣氛之高溫環境內,以兩階段加熱進行碳化,藉由熱處理碳化消除不純物及雜質,製得木質素/標準纖維素生質複合碳纖維。A method for converting a raw material composite carbon fiber by using a raw material, comprising at least the following steps: Dissolving the raw material raw material program: separating the raw material into more than 90% solid lignin particles by using a solvent, and the lignin particles and the standard cellulose After mixing, special ionic liquid is mixed and stirred to uniformly disperse and dissolve the lignin/standard cellulose mixture, and prepare a spinning solution of 1-15 wt%, and mix the lignin/standard cellulose raw material with the wet spinning equipment. Composite fiber, the ionic liquid removed during the process can be recycled and reused as a spinning solvent; Stabilization/preoxidation procedure: pre-soaking the lignin/standard cellulose raw composite fiber with phenolic resin and placing it in a high-pass oxygen environment Stabilization and pre-oxidation, the structure is subjected to a condensation reaction, and the ring-shaped stable structure is maintained to maintain the surface integrity of the composite fiber to obtain a lignin/standard cellulose raw composite oxidized fiber; and a carbonization procedure: the lignin/standard The cellulose raw composite oxidized fiber is placed in a high temperature environment of an inert atmosphere, and carbonized by two-stage heating, by heat Carbide eliminate impurities and impurities to prepare the lignin / cellulose biomass standard composite carbon fibers. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該溶解生質原料程序係將該木質素微粒與該離子液體混合配製成10~15 wt%溶液,在65~95°C下加熱4~6小時,置於水中成形進行溶解特性評估。The method for converting a raw material composite carbon fiber by using a raw material according to the first aspect of the patent application, wherein the raw material of the raw material is mixed with the ionic liquid to prepare a solution of 10 to 15 wt%. The mixture was heated at 65 to 95 ° C for 4 to 6 hours, and placed in water for evaluation of dissolution characteristics. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該溶解生質原料程序中之木質素微粒與該標準纖維素係以5~10%比例混摻。The method for converting a raw material composite carbon fiber by using a raw material according to the first aspect of the invention, wherein the lignin fine particles in the dissolved raw material raw material are mixed with the standard cellulose system in a ratio of 5 to 10%. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該生質原料係選自稻稈、蔗渣、芒草、狼尾草、柳枝稷、玉米稈、木材及竹子之生質廢棄物。The method for converting a raw material composite carbon fiber by using a raw material according to the first aspect of the patent application, wherein the raw material is selected from the group consisting of rice straw, bagasse, miscanthus, pennisetum, switch grass, corn stalk, wood and bamboo. Biomass waste. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該離子液體與該木質素微粒具有表示其分子與木質素性質相互滲透能力之Hansen溶解參數。A method for converting a biomass composite carbon fiber using a raw material according to the first aspect of the invention, wherein the ionic liquid and the lignin microparticle have a Hansen dissolution parameter indicating the interpenetrability of their molecules with lignin properties. 依申請專利範圍第1或5項所述之利用生質原料轉化生質複合碳 纖維之方法,其中,該離子液體係選自1-丁基-3-甲基咪唑氯(1-Butyl-3-Methylimidazolium Chloride, [BMIM]Cl)、1-丁基-3-甲基咪唑六氟磷酸鹽(1-Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6)、1-丁基-3-甲基咪唑四氟溴酸 (1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM]BF4)、或其他溶解參數與木質素性質相近之離子液體。The method for converting a raw material composite carbon fiber by using a raw material according to claim 1 or 5, wherein the ionic liquid system is selected from the group consisting of 1-butyl-3-methylimidazolium chloride (1-Butyl-3- Methylimidazolium Chloride, [BMIM]Cl), 1-Butyl-3-Methylimidazolium Hexafluorophosphate, [BMIM]PF6, 1-butyl-3-methylimidazole IV Fluorine (1-Butyl-3-Methylimidazolium Tetrafluoroborate, [BMIM] BF4), or other ionic liquids with similar solubility parameters to lignin. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該穩定化/預氧化程序係將該木質素/標準纖維素生質複合纖維與該酚醛樹酯於凝固浴浸泡24小時後放置於氧化爐,以預氧化溫度150~300°C、升溫速率0.5~3°C/min、及持溫時間0~2小時進行穩定化及預氧化。The method for converting a raw material composite carbon fiber by using a raw material according to the first aspect of the patent application, wherein the stabilizing/preoxidizing step is the lignin/standard cellulose raw composite fiber and the phenolic resin. After soaking for 24 hours in the coagulation bath, it is placed in an oxidizing furnace, and is stabilized and pre-oxidized at a pre-oxidation temperature of 150 to 300 ° C, a heating rate of 0.5 to 3 ° C/min, and a holding time of 0 to 2 hours. 依申請專利範圍第1項所述之利用生質原料轉化生質複合碳纖維 之方法,其中,該碳化程序係將該木質素/標準纖維素生質複合氧化纖維置放於氮氣氣氛(>99.99%)之高溫爐內,以升溫速率170~200°C/h加熱至800~900°C,並於1200~1400°C溫度下完成碳化過程。The method for converting a raw material composite carbon fiber by using a raw material according to the first aspect of the patent application, wherein the carbonization program places the lignin/standard cellulose raw composite oxidized fiber in a nitrogen atmosphere (>99.99%) In the high-temperature furnace, the temperature is raised at a heating rate of 170 to 200 ° C / h to 800 to 900 ° C, and the carbonization process is completed at a temperature of 1200 to 1400 ° C.
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