CN1789115A - Method for preparing boron nitride nanometer ring and tube - Google Patents

Method for preparing boron nitride nanometer ring and tube Download PDF

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Publication number
CN1789115A
CN1789115A CN 200510045384 CN200510045384A CN1789115A CN 1789115 A CN1789115 A CN 1789115A CN 200510045384 CN200510045384 CN 200510045384 CN 200510045384 A CN200510045384 A CN 200510045384A CN 1789115 A CN1789115 A CN 1789115A
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boron nitride
nanotube
nitride nanometer
boron
nanometer ring
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CN1326768C (en
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郝霄鹏
吴拥中
李红云
陶绪堂
蒋民华
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Shandong University
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Shandong University
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Abstract

A process for preparing boron nitride nanoring and nanopipe, belonging to the technical field of preparing nano material, which in detail is a process for preparing nano ring and nano pipe by applying the heated solid material producing gas or evaporated solid material producing pressure, the process is carried out under low pressure which avoids the high temperature and high pressure, the equipment needed is simple and mass production of low cost is easily to be realized. The raw material is common chemical agent or chemical materials and the process is simple, which is good for increasing the product yield and reduces the cost; the parameter of the reaction is easy to be monitored and controlled, the reaction mechanism is easy to be researched to find out the critical influencing factors and stabilizes the technological condition in a short time; the invention is also environment-friendly

Description

A kind of method for preparing boron nitride nanometer ring, nanotube
(1) technical field
The present invention relates to utilize the solid matter decomposes to produce gas or the living method of pressing nano materials such as aid preparation nanotube and nano-rings of solid matter vaporization, belong to the nano material preparation technical field.
(2) background technology
Since carbon nanotube in 1991 is found, relevant monodimension nanometer material has the potential application prospect and becomes the emphasis of investigation of materials in electric, light and mechanical aspects, and it has caused physicist, material scholar, chemist's extensive interest.Boron nitride (BN) nanotube is the same with carbon nanotube, and B and N atom form the structure that planar is similar to graphite with the sp2 hybrid state.So, when people are to carbon nanotube research, just are contemplated to and necessarily exist the nanotube that forms by B and N.The carbon nanotube energy gap changes along with the diameter and the chirality of nanotube very sensitively, shows from metal to semi-conductive electrical properties.No matter how BN nanotube then its diameter and chirality changes, energy gap unanimous on the whole is arranged all.Add its other and be different from the characteristic of carbon nanotube,, make it that character than the more approaching practicality of carbon nanotube be arranged at aspects such as high temperature, high strength fibre, semiconductor materials as characteristics such as high temperature resistant and oxidation-resistances.The BN nanotube is the same with carbon nanotube strong toughness and high intensity, can be used to make cutter and mould as carbon nanotube, also can be used as the electron device of nanoscale, the stupalith of nanostructure.And boron nitride nanometer ring to be us find to have very big application prospect at aspects such as field-effect transistor, high temperature semiconductors, single-electronic transistors in the world first.
Just be based on the broad prospect of application of boron nitride nano-tube, scientists has been carried out extensive research to the synthetic of BN nanotube, and has obtained fruitful progress, has developed a variety of methods.Mainly can be divided into several classes such as arc discharge method, arc light method of fusion, high temperature pyrolytic cracking (HTP), nanotube template and laser evaporation method, but these preparation methods or need relatively more expensive equipment or the preparation condition of comparison harshness (as High Temperature High Pressure etc.), productivity ratio is lower, therefore, develop a kind of simple to operate, can low cost, the method for high yield, prepared in high purity boron nitride nano-tube is just significant.
(3) summary of the invention
The invention provides a kind of solid matter decomposes of utilizing and produce gas or the living method of pressing aid preparation boron nitride nanometer ring, nanotube of solid matter vaporization, to realize low-cost in enormous quantities preparation of nano-rings nanotube.
The present invention prepares the method for boron nitride nanometer ring, nanotube, comprises the steps, the addition sequence of material is not limit:
(1) boron source, nitrogenous source and the solid matter that adds thermogenesis gas are mixed, direct compression or join compressing tablet in the stainless steel sleeve is put into reaction vessel again, vacuumizes, and charges into nitrogen or argon gas, is heated to 400~800 ℃, reaction 10min~5hr;
(2) after reaction is finished, product deionized water wash, suction filtration, or, carry out suction filtration again, till filtrate is neutrality with after alkalescence, acidic substance or the organic solution processing;
(3) resulting product is heated to 40~100 ℃ and carries out drying, obtains boron nitride nanometer ring or nanotube.
In the above-mentioned steps (1) raw material joined and carry out compressing tablet in the stainless steel sleeve, press the sleeve of knot raw material to put into reaction vessel, allow raw material,, can prepare the nanotubes of different sizes by the shape and the size of regulating sleeve at the sleeve internal reaction with being equipped with.
In the above-mentioned steps (1), the molar ratio of boron source and nitrogenous source is 4: 1~1: 4, and the boron source is 1: 1~1: 6 with the molar ratio that adds the solid matter of thermogenesis gas;
The boron source of using in the above-mentioned steps (1) comprises the organism of simple substance, oxide compound, borate, hydroborate, boron fluoride or the boron of boron, B, B specifically 2O 3, H 3BO 3, Na 3BO 3, NaBH 4, KBH 4Or KBF 4
The nitrogenous source of above-mentioned steps (1) comprises nitride, azide, ammonia, halogenation ammonia or organic amine, requires nitrogen-atoms wherein to be easy to participate in reaction; Described nitride is selected from Li 3N, Na 3N, K 3One of N or its combination, azide is NaN 3, halogenation ammonia is selected from NH 4Cl, NH 4Br, NH 4One of I, organic amine are selected from one of urea, aniline, Trimethylamine 99.
The easy solid matter that produces gas of heating is selected from S, I, Na in the above-mentioned steps (1) 2CO 3, K 2CO 3, NH 4Cl or NH 4I.
Alkaline matter described in the above-mentioned steps (2) is sodium hydroxide or potassium hydroxide; Acidic substance are hydrochloric acid or dithiocarbonic anhydride; Organic solution is acetone or tetracol phenixin.
The notable feature characteristics of present method are: preparation boron nitride nano-tube or nano-rings are in the low pressure reaction condition, have avoided extreme conditions such as High Temperature High Pressure, and the equipment that needs is fairly simple, are easy to realize low-cost production in enormous quantities the in enormous quantities.
The present invention has following advantage: 1. cost is low.Raw materials used chemical reagent commonly used or the industrial chemicals of being, schedule of operation is simple, helps improving productive rate, reduces cost.2, the various parameters in the reaction process (temperature, pressure, ratio etc.) are easy to monitoring and control, and this makes us can easier research reaction mechanism, finds out the influence factor of most critical, as early as possible the stabilization process condition.3, low in the pollution of the environment.The inventive method is decontamination fundamentally, helps environment protection.
(4) description of drawings
Fig. 1 is the x-ray diffraction pattern of the boron nitride nanometer ring of embodiment 1 preparation.
Fig. 2 is the x-ray photoelectron power spectrum of the boron nitride nanometer ring of embodiment 1 preparation.
Fig. 3 is the infrared spectra of the boron nitride nanometer ring of embodiment 1 preparation.
Fig. 4 is the boron nitride nanometer ring scanning and the high explanation electromicroscopic photograph of embodiment 1 preparation.
Fig. 5 is the boron nitride nano-tube scanned photograph of embodiment 2 preparations.
(5) embodiment
Embodiment 1: the preparation of boron nitride nanometer ring
The raw material of preparation boron nitride nanometer ring is H 3BO 3, Li 3N and S.
At first with 0.31g H 3BO 3, 0.17g Li 3N and 0.16gS mix after grinding, and at the 20MPa compressing tablet, put into silica tube then, silica tube is vacuumized processing after, charge into the Ar gas of 1atm again.Silica tube be heated to 600 ℃ the insulation 1 hour after, cool to room temperature naturally after, product is at first handled with dithiocarbonic anhydride, to remove sulphur contained in the product, use deionized water wash, suction filtration 3-5 time then.Resulting like this product just obtains boron nitride nanometer ring after 80 ℃ of dryings.
Shown in Figure 1 is the boron nitride nanometer ring x-ray diffraction pattern for preparing in the present embodiment, and the crystal property of sample and purity are all relatively good as seen from the figure, only contains six side's phase boron nitrides.Fig. 2 is the x-ray photoelectron power spectrum of the boron nitride nanometer ring of present embodiment preparation, and ultimate analysis can be determined thus, and sample is boron nitride really, and can determine that by the peak area of boron and nitrogen the ratio of boron and nitrogen is about 1: 1 in the sample.Fig. 3 is the infrared spectra of the boron nitride nanometer ring of present embodiment preparation, in the spectrum 1384 and 815cm -1Corresponding two characteristic infrared absorption peaks of hexagonal boron nitride.Fig. 4 is the boron nitride nanometer ring scanning and the high explanation electromicroscopic photograph of present embodiment preparation, by the ring texture that can obviously see boron nitride among the figure.
Embodiment 2: the preparation of boron nitride nano-tube
The raw material of preparation boron nitride nano-tube is H 3BO 3, LiN 3And S.
At first with 0.31g H 3BO 3, 0.17g Li 3N and 0.16gS mix after grinding, and with the 20MPa compressing tablet, sleeve are put into silica tube with raw material in diameter is the stainless steel sleeve of 6mm, then silica tube is vacuumized processing after, charge into the Ar gas of 1atm again.Silica tube be heated to 700 ℃ the insulation 1 hour after, cool to room temperature naturally after, product is at first handled with dithiocarbonic anhydride, to remove sulphur contained in the product, use deionized water wash, suction filtration 3-5 time then.Resulting like this product just obtains boron nitride nano-tube after 80 ℃ of dryings.
Fig. 5 is the boron nitride nano-tube scanned photograph of present embodiment preparation, by the tubular structure that can obviously see boron nitride among the figure.
Embodiment 3: the preparation of boron nitride nanometer ring
The raw material of preparation boron nitride nanometer ring is H 3BO 3, LiN 3And NH 4Cl.
At first with 0.31g H 3BO 3, 0.17g Li 3N and 0.27gNH 4Mix after Cl grinds,, put into silica tube then at the 20MPa compressing tablet, silica tube is vacuumized processing after, charge into the N of 1atm again 2Silica tube was heated to 600 ℃ of insulations after 1 hour, cool to room temperature naturally after, with product usefulness deionized water wash, suction filtration 3-5 time.Resulting like this product just obtains boron nitride nanometer ring after 80 ℃ of dryings.
Embodiment 4: the preparation of boron nitride nano-tube
The raw material of preparation boron nitride nano-tube is H 3BO 3, Li 3N and NH 4Cl.
At first with 0.31g H 3BO 3, 0.17g Li 3N and 0.27gNH 4Mix after C grinds, in diameter is the stainless steel sleeve of 6mm,, sleeve put into silica tube with raw material with the 20MPa compressing tablet, then silica tube is vacuumized processing after, charge into the N of 1atm again 2Silica tube was heated to 700 ℃ of insulations after 1 hour, cool to room temperature naturally after, with product usefulness deionized water wash, suction filtration 3-5 time.Resulting like this product just obtains boron nitride nano-tube after 80 ℃ of dryings.
Embodiment 5: the preparation of boron nitride nanometer ring
The preparation method is identical with embodiment 1, and different is with H 3BO 3Be changed to NaBH 4
Embodiment 6: the preparation of boron nitride nanometer ring
The preparation method is identical with embodiment 1, and different is with H 3BO 3Be changed to NaBF 4
Embodiment 7: the preparation of boron nitride nanometer ring
The preparation method is identical with embodiment 1, and different is with H 3BO 3Be changed to B 2O 3
Embodiment 8: the preparation of boron nitride nanometer ring
The preparation method is identical with embodiment 1, and different is with Li 3N is changed to NaN 3
Embodiment 9: the preparation of boron nitride nano-tube
The preparation method is identical with embodiment 2, and different is with H 3BO 3Be changed to NaBH 4
Embodiment 10: the preparation of boron nitride nano-tube
The preparation method is identical with embodiment 2, and different is with H 3BO 3Be changed to NaBF 4
Embodiment 11: the preparation of boron nitride nano-tube
The preparation method is identical with embodiment 2, and different is with H 3BO 3Be changed to B 2O 3
Embodiment 12: the preparation of boron nitride nano-tube
The preparation method is identical with embodiment 2, and different is with Li 3N is changed to NaN 3

Claims (7)

1, a kind of method for preparing boron nitride nanometer ring, nanotube is characterized in that, comprises the steps, the addition sequence of material is not limit:
(1) boron source, nitrogenous source and the solid matter that adds thermogenesis gas mix, and compressing tablet or join compressing tablet in the stainless steel sleeve is put into reaction vessel again, vacuumizes, and charges into nitrogen or argon gas, is heated to 400~800 ℃, reaction 10min~5hr;
(2) after reaction is finished, product deionized water wash, suction filtration, or, carry out suction filtration again, till filtrate is neutrality with after alkalescence, acidic substance or the organic solution processing;
(3) resulting product is heated to 40~100 ℃ and carries out drying, obtains boron nitride nanometer ring or nanotube.
2, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1, it is characterized in that, in the step (1) raw material joined and carry out compressing tablet in the stainless steel sleeve, press the sleeve of knot raw material to put into reaction vessel with being equipped with, allow raw material at the sleeve internal reaction, by the shape and the size of regulating sleeve, can prepare the nanotube of different sizes.
3, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1 is characterized in that, the molar ratio of boron source and nitrogenous source is 4: 1~1: 4 in the step (1), and the boron source is 1: 1~1: 6 with the molar ratio that adds the solid matter of thermogenesis gas.
4, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1, it is characterized in that, the boron source of using in the step (1) comprises the organism of simple substance, oxide compound, borate, hydroborate, boron fluoride or the boron of boron, 3, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1, it is characterized in that the boron source of using in the step (1) is B, B 2O 3, H 3BO 3, Na 3BO 3, NaBH 4, KBH 4Or KBF 4
5, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1, it is characterized in that, the nitrogenous source that uses in the step (1) comprises nitride, azide, ammonia, halogenation ammonia and organic amine, requires nitrogen-atoms wherein to be easy to participate in reaction, and described nitride is selected from Li 3N, Na 3N, K 3One of N or its combination, azide is NaN 3, halogenation ammonia is selected from NH 4Cl, NH 4Br, NH 4One of I, organic amine are selected from one of urea, aniline, Trimethylamine 99.
6, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1 is characterized in that, the solid matter that the heating of using in the step (1) easily produces gas is selected from S, I, Na 2CO 3, K 2CO 3, NH 4Cl or NH 4I.
7, the method for preparing boron nitride nanometer ring, nanotube as claimed in claim 1 is characterized in that, the alkaline matter described in the step (2) is sodium hydroxide or potassium hydroxide; Acidic substance are hydrochloric acid or dithiocarbonic anhydride; Organic solution is acetone or tetracol phenixin.
CNB200510045384XA 2005-12-20 2005-12-20 Method for preparing boron nitride nanometer ring and tube Expired - Fee Related CN1326768C (en)

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100441512C (en) * 2006-12-14 2008-12-10 天津理工大学 Prepn process of nanometer titania ring
CN101428813B (en) * 2008-12-17 2010-12-08 哈尔滨工业大学深圳研究生院 Process for producing ultra-fine boron nitride continuous nano-fibre
CN101928915A (en) * 2010-06-13 2010-12-29 哈尔滨工业大学 Method for plating boron nitride film on surface of one-dimensional nano material
CN101381887B (en) * 2007-09-05 2012-02-15 中国科学院物理研究所 Single crystal boron nanotaper, method for preparing same and applications in electricity and field emission device
CN104058372A (en) * 2014-07-09 2014-09-24 河北工业大学 Preparation method of hexagonal boron nitride nanosheets
CN104891454A (en) * 2015-05-15 2015-09-09 蔡奕荃 Preparation method for boron nitride nanotube
CN107640751A (en) * 2016-07-22 2018-01-30 中国科学院苏州纳米技术与纳米仿生研究所 One-dimensional boron nitride nano material and preparation method thereof
CN107673318A (en) * 2016-08-01 2018-02-09 中国科学院苏州纳米技术与纳米仿生研究所 Boron nitride nano-tube and its batch preparation
CN114852976A (en) * 2022-06-09 2022-08-05 桂林理工大学 Hollow boron nitride short rod and preparation method thereof

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JPS61295211A (en) * 1985-06-24 1986-12-26 Mitsui Toatsu Chem Inc Production of fine powder of high-purity amorphous boron nitride
CN1281481C (en) * 2004-07-08 2006-10-25 北京理工大学 Process for preparing boron nitride nano tube

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100441512C (en) * 2006-12-14 2008-12-10 天津理工大学 Prepn process of nanometer titania ring
CN101381887B (en) * 2007-09-05 2012-02-15 中国科学院物理研究所 Single crystal boron nanotaper, method for preparing same and applications in electricity and field emission device
CN101428813B (en) * 2008-12-17 2010-12-08 哈尔滨工业大学深圳研究生院 Process for producing ultra-fine boron nitride continuous nano-fibre
CN101928915A (en) * 2010-06-13 2010-12-29 哈尔滨工业大学 Method for plating boron nitride film on surface of one-dimensional nano material
CN101928915B (en) * 2010-06-13 2012-09-19 哈尔滨工业大学 Method for plating boron nitride film on surface of one-dimensional nano material
CN104058372B (en) * 2014-07-09 2016-03-30 河北工业大学 A kind of preparation method of hexagonal boron nitride nanosheet
CN104058372A (en) * 2014-07-09 2014-09-24 河北工业大学 Preparation method of hexagonal boron nitride nanosheets
CN104891454A (en) * 2015-05-15 2015-09-09 蔡奕荃 Preparation method for boron nitride nanotube
CN107640751A (en) * 2016-07-22 2018-01-30 中国科学院苏州纳米技术与纳米仿生研究所 One-dimensional boron nitride nano material and preparation method thereof
CN107640751B (en) * 2016-07-22 2020-03-27 中国科学院苏州纳米技术与纳米仿生研究所 One-dimensional boron nitride nano material and preparation method thereof
CN107673318A (en) * 2016-08-01 2018-02-09 中国科学院苏州纳米技术与纳米仿生研究所 Boron nitride nano-tube and its batch preparation
CN107673318B (en) * 2016-08-01 2020-11-27 中国科学院苏州纳米技术与纳米仿生研究所 Boron nitride nanotubes and batch preparation method thereof
CN114852976A (en) * 2022-06-09 2022-08-05 桂林理工大学 Hollow boron nitride short rod and preparation method thereof
CN114852976B (en) * 2022-06-09 2023-06-23 桂林理工大学 Hollow boron nitride short rod and preparation method thereof

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