TW201214466A - Dispersing agent of MWCNTs and the method for preparation of homogeneous MWCNTs dispersion - Google Patents
Dispersing agent of MWCNTs and the method for preparation of homogeneous MWCNTs dispersion Download PDFInfo
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- TW201214466A TW201214466A TW099131660A TW99131660A TW201214466A TW 201214466 A TW201214466 A TW 201214466A TW 099131660 A TW099131660 A TW 099131660A TW 99131660 A TW99131660 A TW 99131660A TW 201214466 A TW201214466 A TW 201214466A
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- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000002270 dispersing agent Substances 0.000 title claims abstract description 10
- 239000002048 multi walled nanotube Substances 0.000 title abstract description 16
- 239000006185 dispersion Substances 0.000 title abstract description 7
- 229910021397 glassy carbon Inorganic materials 0.000 claims abstract description 18
- 239000011521 glass Substances 0.000 claims abstract description 13
- FPVGTPBMTFTMRT-NSKUCRDLSA-L fast yellow Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-NSKUCRDLSA-L 0.000 claims abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 71
- 239000002041 carbon nanotube Substances 0.000 claims description 64
- 229910021393 carbon nanotube Inorganic materials 0.000 claims description 63
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 claims description 26
- 239000000243 solution Substances 0.000 claims description 24
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 claims description 14
- 235000019233 fast yellow AB Nutrition 0.000 claims description 14
- 229960003638 dopamine Drugs 0.000 claims description 13
- 239000007864 aqueous solution Substances 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 230000002378 acidificating effect Effects 0.000 claims description 6
- 229910021392 nanocarbon Inorganic materials 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000011718 vitamin C Substances 0.000 claims description 4
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 241000238413 Octopus Species 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000010408 film Substances 0.000 abstract description 11
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 abstract description 6
- 239000010409 thin film Substances 0.000 abstract description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 3
- 239000002114 nanocomposite Substances 0.000 abstract description 2
- 238000005119 centrifugation Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000000758 substrate Substances 0.000 description 7
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000075 oxide glass Substances 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000002071 nanotube Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 238000004626 scanning electron microscopy Methods 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 102100024133 Coiled-coil domain-containing protein 50 Human genes 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 101000910772 Homo sapiens Coiled-coil domain-containing protein 50 Proteins 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000002484 cyclic voltammetry Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012154 double-distilled water Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- RHZWSUVWRRXEJF-UHFFFAOYSA-N indium tin Chemical compound [In].[Sn] RHZWSUVWRRXEJF-UHFFFAOYSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/158—Carbon nanotubes
- C01B32/168—After-treatment
- C01B32/174—Derivatisation; Solubilisation; Dispersion in solvents
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2202/00—Structure or properties of carbon nanotubes
- C01B2202/06—Multi-walled nanotubes
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nanotechnology (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Composite Materials (AREA)
- Dispersion Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Carbon And Carbon Compounds (AREA)
Description
201214466 六、發明說明: 【發明所屬之技術領域】 散奈来碳管並使之 本發明侧於—縣米碳管分散劑及分 處於穩定態的方法。 【先前技術】
不米碳e (CNTs)及其奈米複合物近年來已被廣泛利用於 材料科學及X㈣面。由於奈米碳管兼具觸㈣子、機械、 化學及熱性質’引起了各界的興趣。 奈米碳管可朗在包括在電化學元件、場發就件、夺 米級的電子元件及感·等等,其應關面可以說相當廣泛, 但要應用奈米碳管,卻還是有—些限制。目前這方面的研究 中’最主要的挑戰,是在不同的溶齡質中使奈米碳管均句分 散,並保持穩疋的狀態,特別是在水溶液中。不幸的是,實際 上很難做到這-點。這是由於奈米碳管之間的凡得瓦作用力 (Van derWaals interaction)很強,使奈米碳管合成後呈現糾結 在一起的狀態。近年來,有許多研究致力於利用溶液與奈米碳 管之間的物理性作用力,使奈米碳管能分散於溶液中,包括使 用表面活性劑或高分子。在製備電化學感測器時,奈米碳管也 可以用來修飾電極(modified electrode)來提高靈敏度。 多巴胺(dopamine,以下簡稱DA)是哺乳類動物作為神經 傳遞介質(neurotransmitter)或荷爾蒙(hormone)中不可或缺的 成分,其主要提供移動、學習、記憶及信號回覆等功能。左旋 雉生素C (L-Ascorbic acid,以下簡稱AA)則是大量的被使用 在食物、飲料、動物飼料、藥劑配方及化妝品中作為抗氧化劑, 201214466 也是人類的營養基本成分中,主要的可溶性的抗氧化劑。因 此’常會利用電化學感測器來偵測DA或AA。 但DA及AA在裸露的固態電極上會發生氧化,並且, DA及AA是發生在相同的電位範圍,所以很難以電化學方式 選擇及同步進行偵測。另外,DA及AA氧化後的產物也會吸 附在電極表面造成電極污染,針對未修飾的電極來說,這些都 疋很主要的問題。 因此,透過添加奈米碳管到聚合物基質(p〇|ymer matrices)中’來改變電極原本的電化學、光學或其他介面的性 質,克服上述問題,是一個有效的方式。但在此之前,使奈米 碳管分散是目前所遇到的挑戰。 【發明内容】 有鑑於此,本發明提供一種奈米碳管的分散劑及使奈米 碳管穩定處於分散狀態的方法。係利用酸性黃色9號 (4-amino-1-1 •azobenzene-SW-disulfonic acid,AY)之水溶液 作為分散劑,可使多壁奈米碳管均勻散佈於酸性黃色9號溶液 中,並可穩定維持一段時間。 奈米奴管溶於酸性黃色9號水溶液,並施以擾拌使奈米 碳管均勻散佈於酸性黃色9號水溶液中,製備成一奈米碳管/ 酸性黃色9號溶液。 另外,將奈米碳管/酸性黃色9號溶液’塗佈在一導電玻 璃或一玻璃碳電極(glassy carbon electrode,GCE)上後,將導電 玻璃或該玻璃碳電極乾燥後,形成一奈米碳管/酸性黃色9號薄 膜於導電玻璃或玻璃碳電極上。 並以附著奈米碳管/酸性黃色9號薄膜的玻璃碳電極 4 201214466 (GCE)做為工作,施以—電化學聚合法,於朗碳_上 (GCE)形成聚合_性黃色9號(ΡΑγ)/奈米碳管。 本發明更提供崎合的離黃色9撕卿奈米碳管修 飾的該玻璃碳電極作為電化學感測器之電極,可用以姻多巴 胺(DA)及左旋維生素c(AA)。 ' 利用本㈣之雜黃色9號驗作為分㈣可使多壁奈 米碳管均勻分散’並可穩定維持-段時間。並且,應用在修飾
電化學感測H之電極時’可提高侧多巴_A)及左旋維 C(AA)的靈敏度。 【實施方式】 ^為使本發明之上述目的、特徵和優點能更明顯易 懂’下文依本發明奈米碳管的分制及使奈米碳管穩定處於 分散狀態的方法’特舉較佳實施例,並配合所附相關圖 式’作詳細說明如下。 本發明奈米碳管的分散劑可以使奈米碳管均勻散 佈,並可穩定維持一段時間。本發明中是使用酸性黃色9號 (4-amino-1-r-azobenzene_34,_d|Su|f〇nic acjd 以下簡稱^ 之水溶液作為奈米碳管之分散劑,其中Αγ是溶於去離子水 中,莫耳濃度大約0.1至25 mM,對於分散奈米碳管而言, 才會有較佳的效果。 ° 在本發明實施例中,是將多壁奈米碳管(MWCNTs)分散於 濃度大約2.5 mM的AY溶液中。首先,將10 mg的奈米 碳管溶於10 mL的AY溶液中,用超音波震動1〇;鐘 後,再攪拌三個小時,使奈米碳管均勻分散於Αγ溶液 中。經過實驗證明,奈米碳管在ΑΥ溶液放置於室溫下, 可以維持均勻分散的狀態達三個月之久。 201214466 其中,奈米碳管於AY溶液中的濃度大約0.1至10 mg/mL可以得到較佳的分散效果。而進一步的實驗中, 為了最佳化奈米碳管的濃度,將濃度0.5、1、1.5及 2mg/mL的溶液相互比較,發現當濃度為1 mg/mL時, 奈米碳管可以非常穩定的分散於AY溶液中。 AY可以具有良好的分散能力可以被解釋是由於其 在奈米碳管上的吸附滞後(adsorption hysteresis)現 象。因為不同的機制可能同時作用,主要的有疏水性作 用(hydrophobic interaction)、π鍵鍵結、靜電作用力 以及氫鍵的鍵結等等。奈米碳管中的每一個碳原子具有 一個垂直於表面的π電子軌域,因此,具有π電子的有 機分子,比如’具有碳雙鍵(c=c)或苯環,可以和奈 米碳管形成π-π鍵。可以參照圖1,為多壁奈米碳管被 ΑΥ分散之示意圖。其中圖ία為叢集成一團的奈米碳 管10,圖1Β是經過ΑΥ 11分散穩定後之奈米碳管1〇。 接著,將奈米碳管/ΑΥ溶液,在導電玻璃,如:氧 化銦錫(ΙΤ0) ’或電化學感測器的玻璃碳電極(g丨assy carbon electrode, GCE)上乾燥形成薄膜後,用來修飾 電極。 本發明實施例中’將奈米碳管/AY溶液,在導電玻 璃基板上乾燥形成薄膜的步驟包括:首先將2〇〇 的 奈米碳管/AY溶液塗佈(coat 〇nt〇)在氧化銦錫玻璃基 板’接著將氧化銦錫玻璃基板放置於烘箱中升溫到6〇 C ’持溫30分鐘’使奈米碳管/AY於氧化銦錫玻璃基 板上乾燥,形成薄膜。 本發明並將奈米碳管溶於一般去離子水中,並以 201214466 2方式’在氧化轉朗基板上形成奈米碳管薄膜作 為對照組。請參關2,為本發财,利用掃描式電子 顯微鏡(SEM)觀察奈米碳管/Αγ溶液乾燥後形成薄膜於 乳化銦錫玻璃基板上的結果。由圖2中可看出,利 發明奈来破管/ΑΥ溶液所製備的薄膜,奈米碳管的分布 均勾。由此可證明,ΑΥ針對奈米碳管而言是—個良好 的分散劑’並且不需要針對奈米碳管做什麼複雜或特殊
,處理,即可在導電玻璃上製備—層均勻分散的奈米碳 官0 以類似的方式也可以將奈米碳管/ Αγ溶液,在玻璃 碳電極(GCE)上乾燥形成薄膜,在本發明實施例中, 是將10PL的奈米碳管/AY溶液塗佈在已經預先清潔過 的玻璃碳電極,接著同樣放入烘箱中在6〇。〇,持溫 分鐘’使奈米碳管/AY於玻璃碳電極(GCE)上乾燥形成 薄膜。 + 接著,再施以電化學聚合法,以探討奈米碳管/Αγ 薄膜氧化還原與聚合特性。電化學聚合是利用習知的三 極系統,其中,奈米碳管/ΑΥ薄膜修飾的玻璃碳電^ (GCE)或導電玻璃做為工作電極,而以白金線及 Ag/AgCI分別作為輔助電極及參考電極。 本發明實施例中,是將奈米碳管/AY薄膜修飾的玻 螭碳電極(GCE)以雙蒸餾水(double distilled water)清 洗之後’將奈米碳管/AY薄膜修飾的玻璃碳電極e) 做為工作電極,在0.1M的硫酸水溶液(HAO4)以循環 伏安法在-0.5至2V的範圍内,以每秒〇_〇5V的速率作 來回掃描。從電壓·電流(CV)測量結果,可以知道即便【 201214466 是以蒸餾水清洗之後,AY分子仍牢牢吸附在奈米碳管 上。 AY聚合後的高分子結構預期會和聚笨胺 (polyaniline)相似,而經過電化學聚合後的AY/奈米碳 管/玻璃碳電極(GCE)會再次以蒸餾水清洗,並於室溫下 放置30分鐘乾燥。 除此之外,本發明並利用已聚合 AY(p0|ymerized-AY)/奈米碳管/玻璃碳電極(GCE)作為 • 電極來偵測多巴胺(DA)及左旋維他命C(AA),相較於未 修飾的玻璃碳電極而言,具有更高靈敏度。並且,同時 偵剛多巴胺(DA)及左旋維生素C(AA)時’也可以很輕易 分別二者的訊號。 ^ 本發明雖以較佳實例闡明如上’然其並非用以限 定本發明精神與發明實體僅止於上述實施例。凡熟悉此 項技術者,當可輕易了解並利用其它元件或方式來產生 相同的功效。是以,在不脫離本發明之精神與範疇内所 _ 作之修改,均應包含在下述之申請專利範圍内。 201214466 【圖式簡單說明】 圖1A及圖1B分別顯 後之不思圖,及 $奈米碳管被酸性黃色9號(AY)分散前 圖2顯示利用掃描式電子顯微鏡(SEM)觀察本發明之 奈米碳管/AY溶液乾燥後形成薄膜於氧化銦錫玻璃基板 上的結果。 【主要元件符號說明】 奈米碳管10 酸性黃色9號11
Claims (1)
- 201214466 七、申請專利範圍: 1’種夕壁奈米碳管分散劑,用以使奈米碳管均勻散佈於該溶 液中’並可穩定維持一段時間,該溶液為酸性黃色9號 (4 amino-1-1 _az〇benzene_3 4'-disulfonic acid, AY)之水溶液。 2·如申請專利範圍第1項所述的溶液,其中酸性黃色9號是溶 於去離子水中,莫耳濃度大約 0.1 至 25mM。 3. 種使奈米碳管分散的方法,包括: 製備一酸性黃色9號的水溶液;及 將一預定重量之奈米碳管溶於該酸性黃色9號水溶液,並施 以擾拌使奈米;6炭管均勻散佈於該酸性黃色9號水溶液中,製備 成一奈米碳管/酸性黃色9號溶液。 4. 如申請專利範圍第3項所述的方法,其中該酸性黃色9號水 溶液的莫耳濃度大約0.1至25 mM。 5·如申請專利翻第4項所述龄法,其巾絲碳管溶於該酸 性黃色9號水溶液中之濃度大約〇」〜1〇 mg/m(_。 6·如申請專利範圍第3項所述的方法,更包括將該奈来碳管/ 酸性黃色9餘液,塗佈在—導電玻璃或—㈣碳電極 (glassy carbon e|ectrode,GCE)上後,將該導電破璃或 該玻璃碳電極錢,形H切㈤雜黃色9號薄膜於 該導電玻璃或該玻璃碳電極上。 、、 201214466 7·如申請專利範圍第6頊所述的方法,更包括以附著奈米碳管 /酸性黃色9號薄膜的該玻璃碳電極(GCE)做為工作電 極,施以一電化學聚合法,於該玻璃碳電極上(GCE)形成聚合 的酸性黃色9號(PAY)/奈米碳管。 8·如:請專利範圍第7項所述的方法’更包括以聚合的 色9號(PAY)/奈管修飾的該玻璃碳電極作為電化學 “則器之電極’用以細】多巴胺(DA)及左旋維生素C(AA)。
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| US12/953,525 US20120070566A1 (en) | 2010-09-17 | 2010-11-24 | Dispersing Agent of MWCNTs and the Method for Preparation and Application of Homogeneous MWCNTs Dispersion |
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