CN100455509C - Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid - Google Patents

Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid Download PDF

Info

Publication number
CN100455509C
CN100455509C CNB2007100676866A CN200710067686A CN100455509C CN 100455509 C CN100455509 C CN 100455509C CN B2007100676866 A CNB2007100676866 A CN B2007100676866A CN 200710067686 A CN200710067686 A CN 200710067686A CN 100455509 C CN100455509 C CN 100455509C
Authority
CN
China
Prior art keywords
cnt
suspension
weibull
mixed
tannic acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CNB2007100676866A
Other languages
Chinese (zh)
Other versions
CN101049925A (en
Inventor
林道辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang University ZJU
Original Assignee
Zhejiang University ZJU
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang University ZJU filed Critical Zhejiang University ZJU
Priority to CNB2007100676866A priority Critical patent/CN100455509C/en
Publication of CN101049925A publication Critical patent/CN101049925A/en
Application granted granted Critical
Publication of CN100455509C publication Critical patent/CN100455509C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

This invention discloses a method for preparing stable carbon nanotube (CNT) suspension by using tannic acid. The method comprises: (1) affing distilled water into tannic acid to obtain 5-500 mg/L tannic acid aqueous solution; (2) adding CNT (inner diameters less than or equal to 100 nm) to obtain 10-1000 mg/L CNT solution; (3) ultrasonicating in an ultrasonic cleaner for 30-60 min; (4) standing for more than 24 h, transferring the CNT suspension into another container. The dispersant in this invention, tannic acid, is a nontoxic and water-soluble natural product, and has high suspension ability to CNT. The obtained CNT suspension is stable, and the method is suitable for a wide range of conditions.

Description

Utilize Weibull to make the method for stable carbon nanotube suspension
Technical field
The present invention relates to a kind of method of utilizing Weibull to make stable carbon nanotube suspension.
Background technology
Nanosecond science and technology develop rapidly, will produce wide influence to global social economy.At present, the nano material industrialization is in the ascendant in the whole nation even global range.CNT (carbon nano-tube) is the nano material that a class has the unique physical chemical attribute, and its application in every field has caused various countries scientist and entrepreneur's common concern.But because the relative caliber of length of CNT (carbon nano-tube) is very big, add the Van der Waals force effect, twine easily with agglomerated together between the carbon pipe, be difficult to form uniform and stable suspension, this is a subject matter of restriction CNT (carbon nano-tube) widespread use.
At present, mostly adopt tensio-active agents such as Triton X-100 to make the suspension of CNT (carbon nano-tube) as dispersion agent.But the amount of required tensio-active agent is bigger, generally will reach 1% concentration, and cost is bigger, and some is poisonous, is easy to generate pollution.A kind of simple and effective dispersion agent and dispersing method will promote the industrialized development of CNT (carbon nano-tube).
Weibull claims that again tannin or tannin are the compounds of a class complexity, nontoxic and soluble in water, be present in many plants (as pomegranate, coffee, tealeaves, persimmon etc.), the structure of the Weibull of different sources is variant, but all has the polyphenol hydroxyl structure, have hydrophilic, lipophilic parents' characteristic, certain surfactivity is arranged, be used in the industries such as printing and dyeing, surface treatment.Its hydrophobic end can be by CNT (carbon nano-tube) surface strong adsorption, and the aqueous solution is stretched in its hydrophobic side, thereby can play the effect that disperses with suspended nano carbon pipe.
Summary of the invention
The purpose of this invention is to provide a kind of method of utilizing Weibull to make stable carbon nanotube suspension.
Comprise the steps:
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 5~500mg/L;
2) in the above-mentioned Weibull aqueous solution, add the CNT (carbon nano-tube) of internal diameter≤100nm, be mixed with the mixed solution that the CNT (carbon nano-tube) mass concentration is 10~1000mg/L;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 30~60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
Advantage of the present invention
1) Weibull of the present invention's use is a class natural product, and is nontoxic and soluble in water, is present in many plants (as pomegranate, coffee, tealeaves, persimmon etc.).
2) Weibull is strong to the suspending power of CNT (carbon nano-tube), the CNT (carbon nano-tube) effect suspension stabilization of making.Relatively use the multiple-wall carbon nanotube (MWCNT of the 200mg/L that Weibull (available from the Alfa Aesar A Johnson Matthey Company of the U.S.) aqueous solution (pH=4) of 100mg/L is mixed with, the MWCNT mixed solution of internal diameter 60~100nm) mixed solutions and the 200mg/L that makes with 1% the Triton X-100 aqueous solution was through ultrasonic 60 minutes and leave standstill 4 suspension situations after round the clock, can find that the suspending power of Weibull significantly is better than TritonX-100.By the content of MWCNT in the further test suspension liquid, find the MWCNT that the Weibull aqueous solution of 100mg/L can stable suspersion 75mg/L, its suspending power is 4 times of 1% the Triton X-100 aqueous solution.
3) the working conditions broad of this method.The Weibull pH value of aqueous solution a wider range that is suitable for, the Weibull aqueous solution of pH value in 4~9 scopes all has the good suspension property energy to MWCNT; The concentration range broad of the Weibull aqueous solution that is suitable for, (the stable suspersion concentration of 60~100nm) mixed solutions is all greater than 50mg/L to the MWCNT of 200mg/L for the Weibull of 5~500mg/L; Caliber a wider range of the MWCNT that is suitable for, in the Weibull aqueous solution (100mg/L) of 40ml, add the 8mg internal diameter and be<MWCNT of 5 kinds of calibers such as 10nm, 10~20nm, 20~40nm, 40~60nm, 60~100nm, the concentration of MWCNT is 26~142mg/L in the suspension that forms after ultrasonic 60 minutes leave standstill 24 hours, wherein concentration is minimum is that internal diameter is<MWCNT of 10nm, and the highest is that internal diameter is the MWCNT of 20~40nm.
Embodiment
Embodiment 1
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 5mg/L;
2) (internal diameter is that 60~100nm) to be mixed with the CNT (carbon nano-tube) mass concentration be the mixed solution of 200mg/L to add CNT (carbon nano-tube) in the above-mentioned Weibull aqueous solution;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
Embodiment 2
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 100mg/L;
2) (internal diameter<10nm) is mixed with the mixed solution that the CNT (carbon nano-tube) mass concentration is 200mg/L to add CNT (carbon nano-tube) in the above-mentioned Weibull aqueous solution;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 30 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
Embodiment 3
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 100mg/L;
2) (internal diameter is that 60~100nm) to be mixed with the CNT (carbon nano-tube) mass concentration be the mixed solution of 10mg/L to add CNT (carbon nano-tube) in the above-mentioned Weibull aqueous solution;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
Embodiment 4
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 100mg/L;
2) (internal diameter is that 60~100nm) to be mixed with the CNT (carbon nano-tube) mass concentration be the mixed solution of 500mg/L to add CNT (carbon nano-tube) in the above-mentioned Weibull aqueous solution;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
Embodiment 5
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 500mg/L;
2) (internal diameter is that 60~100nm) to be mixed with the CNT (carbon nano-tube) mass concentration be the mixed solution of 200mg/L to add CNT (carbon nano-tube) in the above-mentioned Weibull aqueous solution;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.

Claims (1)

1, a kind of method of utilizing Weibull to make stable carbon nanotube suspension is characterized in that comprising the steps:
1) Weibull is added distilled water and be mixed with the aqueous solution that mass concentration is 5~500mg/L;
2) in the above-mentioned Weibull aqueous solution, add the CNT (carbon nano-tube) of internal diameter≤100nm, be mixed with the CNT (carbon nano-tube) mass concentration and be 10,200 or the mixed solution of 500mg/L;
3) container that above-mentioned mixed solution will be housed is placed in the ultrasonic cleaning machine ultrasonic 30~60 minutes;
4) mixed solution after the supersound process was left standstill more than 24 hours, then suspension is transferred in another container, stable carbon nanotube suspension.
CNB2007100676866A 2007-03-29 2007-03-29 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid Expired - Fee Related CN100455509C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2007100676866A CN100455509C (en) 2007-03-29 2007-03-29 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2007100676866A CN100455509C (en) 2007-03-29 2007-03-29 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid

Publications (2)

Publication Number Publication Date
CN101049925A CN101049925A (en) 2007-10-10
CN100455509C true CN100455509C (en) 2009-01-28

Family

ID=38781564

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2007100676866A Expired - Fee Related CN100455509C (en) 2007-03-29 2007-03-29 Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid

Country Status (1)

Country Link
CN (1) CN100455509C (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101225247B (en) * 2007-12-27 2011-04-06 江苏奈特纳米科技有限公司 Nano material additive
CN103803523A (en) * 2013-11-18 2014-05-21 广东电网公司电力科学研究院 Surface modifying and dispersing method of carbon nano-tube
CN104946324B (en) * 2015-05-27 2016-08-24 曹一婕 A kind of synthetic method improving water coal slurry stability additive
CN109046252B (en) * 2018-07-20 2021-06-18 辽宁大学 Carbon nanotube and gallnut tannin composite material, preparation method thereof and application thereof in gallium recovery
CN110128784B (en) * 2019-04-30 2021-11-09 中国林业科学研究院林产化学工业研究所 Preparation method of water-based carbon hybrid material
CN113564664A (en) * 2021-07-29 2021-10-29 合肥工业大学 Preparation method of sintered NdFeB magnet surface modified carbon nanotube enhanced organic coating
CN113817343A (en) * 2021-09-27 2021-12-21 昆明理工大学 Dispersing method of nano carbon material
CN115491070A (en) * 2022-07-27 2022-12-20 昆明理工大学 Preparation method and application of electric-conductive and heat-conductive coating

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1643192A (en) * 2002-01-15 2005-07-20 毫微动力学股份有限公司 Compositions of suspended carbon nanotubes, methods of making the same, and uses thereof
CN1697146A (en) * 2005-03-17 2005-11-16 上海交通大学 Method for structuring field effect transistor in multiple channels from Nano carbon tubes
CN1709792A (en) * 2004-06-16 2005-12-21 东元奈米应材股份有限公司 Nano carbon tube suspensoid and its manufacturing method
US20060006367A1 (en) * 2004-07-06 2006-01-12 Chun-Yen Hsiao Carbon nanotube suspension

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1643192A (en) * 2002-01-15 2005-07-20 毫微动力学股份有限公司 Compositions of suspended carbon nanotubes, methods of making the same, and uses thereof
CN1709792A (en) * 2004-06-16 2005-12-21 东元奈米应材股份有限公司 Nano carbon tube suspensoid and its manufacturing method
US20060006367A1 (en) * 2004-07-06 2006-01-12 Chun-Yen Hsiao Carbon nanotube suspension
CN1697146A (en) * 2005-03-17 2005-11-16 上海交通大学 Method for structuring field effect transistor in multiple channels from Nano carbon tubes

Also Published As

Publication number Publication date
CN101049925A (en) 2007-10-10

Similar Documents

Publication Publication Date Title
CN100455509C (en) Method for preparing suspension liquid of steady Nano carbon tube by using tannic acid
Tang et al. Dye adsorption by self-recoverable, adjustable amphiphilic graphene aerogel
Raval et al. Malachite green “a cationic dye” and its removal from aqueous solution by adsorption
Dutt et al. A review of advances in engineered composite materials popular for wastewater treatment
Bajpai et al. A sustainable graphene aerogel capable of the adsorptive elimination of biogenic amines and bacteria from soy sauce and highly efficient cell proliferation
Ahmed et al. Nanomaterials as a sustainable choice for treating wastewater
Wang et al. One-step hydrothermal preparation of amino-functionalized carbon spheres at low temperature and their enhanced adsorption performance towards Cr (VI) for water purification
Xu et al. Preparation of graphene adsorbents and their applications in water purification
Yu et al. Adsorptive removal of ciprofloxacin by ethylene diaminetetraacetic acid/β-cyclodextrin composite from aqueous solution
Liang et al. Adsorptive removal of gentian violet from aqueous solution using CoFe2O4/activated carbon magnetic composite
Modi et al. Facile one-step synthesis of nitrogen-doped carbon nanofibers for the removal of potentially toxic metals from water
Zhang et al. Ag NPs decorated on the magnetic Fe3O4@ PDA as efficient catalyst for organic pollutants removal and as effective antimicrobial agent for microbial inhibition
Wang et al. Adsorption performance and mechanism of antibiotics from aqueous solutions on porous boron nitride–carbon nanosheets
Verma et al. Green synthesis of carbon-based nanomaterials and their applications in various sectors: a topical review
Mubarik et al. Synthetic approach to rice waste-derived carbon-based nanomaterials and their applications
Rabiee et al. Green (Nano) membranes: A review
Huang et al. Adsorption of antibiotics from wastewater by cabbage-based N, P co-doped mesoporous carbon materials
Du et al. Micro-mechanism insights into the adsorption of anionic dyes using quaternary ammonium-functionalised chitosan aerogels
Zhao et al. Easy-handling carbon nanotubes decorated poly (arylene ether nitrile)@ tannic acid/carboxylated chitosan nanofibrous composite absorbent for efficient removal of methylene blue and congo red
Reddy et al. Graphene-based nanomaterials for the removal of pharmaceuticals in drinking water sources
Fathy et al. Nanostructured activated carbon xerogels for removal of methomyl pesticide
Yu et al. Dual‐Pore Carbon Shells for Efficient Removal of Humic Acid from Water
Elamin et al. Removal of ciprofloxacin and indigo carmine from water by carbon nanotubes fabricated from a low-cost precursor: Solution parameters and recyclability
Zhou et al. Facile preparation of alveolate biochar derived from seaweed biomass with potential removal performance for cationic dye
Wei et al. Ammonia-assisted hydrothermal carbon material with schiff base structures synthesized from factory waste hemicelluloses for Cr (VI) adsorption

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090128

Termination date: 20110329