CN1736585A - Nano carbon fiber/graphite felt compound catalytic material and preparation process thereof - Google Patents
Nano carbon fiber/graphite felt compound catalytic material and preparation process thereof Download PDFInfo
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- CN1736585A CN1736585A CN 200510027814 CN200510027814A CN1736585A CN 1736585 A CN1736585 A CN 1736585A CN 200510027814 CN200510027814 CN 200510027814 CN 200510027814 A CN200510027814 A CN 200510027814A CN 1736585 A CN1736585 A CN 1736585A
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Abstract
The invention discloses a nano carbon fibre/ graphite felt composite catalysis material of a macroscopic dimension and the method for preparation. The composite catalysis material comprises graphite felt, and nano carbon fibre that grows on graphite felt in situation. The technique contains the following steps: liquid-phase or gas-phase oxygenizing graphite felt; soaking the treated graphite felt into water solution containing soluble metallic salt, heating in air condition; heating to 773- 973K in reduction condition and keeping 1-6h, then adding reactivity gas to generate the nano carbon fibre growing reaction on graphite felt in situation. The nano carbon fibre/ graphite felt composite material has a big density, a high mechanical strength, a hollow feature, and a large external surface area, and As a new carbonaceous catalysis material, it is suit for a catalyst carrier, or a catalyst.
Description
Technical field
The present invention relates to a kind of nano carbon fiber/graphite felt compound catalytic material and preparation method thereof with macro-scale.
Background technology
Carbon nano-fiber is the class graphite material of a class quasi-one dimension fibre shape, has unique microstructure, has caused people's extensive concern since the nineties in last century.
Carbon nano-fiber density is low, defective is few, compact structure, specific modulus and specific strength height, can be used as structure and strengthens system and be equipped with high performance composite.Simultaneously, carbon nano-fiber electromagnetic performance excellence, and also corrosion-resistant, high temperature resistant, anti-oxidant, can make electronic device, electrode and electromagnetic shielding material etc.In addition, carbon nano-fiber has the regularly arranged graphite flake layer structure of nanoscale, and abundant border and/or peculiar hollow tube, is special absorption and catalysis material of a class performance.Along with to the going deep into of carbon nano-fiber basic research, the various performance characteristics of carbon nano-fiber will be realized gradually, and are fully used.Therefore, carbon nano-fiber will present wide prospect in industrial application in growing field such as traffic, electronics, the energy, catalysis.
Compare with traditional carbonaceous catalysis materials such as active carbon, carbon nano-fiber is made catalyst or carrier has many advantages, be embodied in: (1) controllable microstructure; (2) interfacial effect is strong; (3) hole characteristic in; (4) Heat stability is good, the mechanical strength height, impurity content is few.Studies show that in recent years, in catalytic process such as selective hydrogenation and dehydrogenation, hydroformylation, synthetic ammonia, desulfurization, NO decomposition, carbon nano-fiber catalyst and carrier have demonstrated excellent catalytic performance.In the storing hydrogen catalyst, carbon nano-fiber also is good reactive metal carrier and hydrogen acceptor.
Usually carbon nano-fiber exists with powder morphology, and the size of powder particle depends on carbon nano-fiber preparation method and growth conditions, and diameter is generally less than 200nm, and length is that μ m～mm does not wait.Carbon nano-fiber is developed to catalyst or catalyst carrier, must makes carbon nano-fiber possess the shape and size of macroscopic view, just can be applicable to the Industrial Catalysis process.As being applied to commercial fixed bed gas-solid catalysis device, the catalyst of powder-type stops up subordinate's pipeline easily by high velocity gas stream, or cause catalyst loss, and the resistance of powder-type beds is big, easily causes kinetic equation loss, and unfavorable to catalytic reaction.For the reaction of commercial tank formula liquid-phase catalysis, the powder-type catalyst separates the comparison difficulty with reactant liquor, therefore is difficult to the catalyst recovery utilization.How to prepare a kind of carbon nano-fiber catalyst with certain macroshape and size, be people the problem very paid close attention to.
Summary of the invention
Technical problem to be solved by this invention provides a kind of carbon nano-fiber catalysis material with macrostructure and preparation method thereof, to adapt to the demand of Industrial Catalysis course of reaction.
Carbon nano-fiber catalysis material with macrostructure of the present invention is composited by the carbon nano-fiber of growth in situ on graphite felt and the graphite felt;
With graphite felt weight is benchmark, and the weight of carbon nano-fiber is 0.5～30 times of graphite felt weight, more preferably 1～20 times, is preferably 3～10 times;
Said graphite felt can adopt business-like product, and as the polyacrylonitrile-radical graphite felt that the emerging carbon element in Shanghai Co., Ltd produces, this is a kind of felt shape material that is formed by the braiding of polyacrylonitrile-radical graphite fibre.Other graphite felt commodity also have viscose glue base graphite felt and asphaltic base graphite felt.The macroshape of graphite felt and size can be carried out cutting as required, as the employing rectangle, and circle etc., thickness is generally 5～10mm;
Nano carbon fiber/graphite felt compound catalytic material of the present invention not only has macroshape and size, and density is big, the mechanical strength height.Because the carbon nano-fiber in the compound catalyze material exists with ecosystem, thereby has kept the microstructure and the physicochemical characteristic of carbon nano-fiber fully.Nano carbon fiber/graphite felt compound catalytic material combines the advantage of two kinds of composition materials, can be made into the catalyst or the catalyst carrier of required form and size, is directly used in the Industrial Catalysis course of reaction.
The preparation method of nano carbon fiber/graphite felt compound catalytic material of the present invention comprises the steps:
(1) pre-treatment of said graphite felt: graphite felt soaked or boils 0.5～24h in salpeter solution or under 573～1073K roasting 1～6h, the mass concentration of salpeter solution with 10%～67% for suitable;
(2) graphite felt that step (1) is obtained is immersed in the aqueous solution that contains soluble metallic salt, can add organic solvent in the aqueous solution, and organic solvent is selected from ethanol, acetone, isopropyl alcohol or ethylene glycol etc., to strengthen the wetability of graphite felt; In the aqueous solution, volume of organic solvent concentration is suitable with 10～60%;
Soluble metallic salt comprises nitrate, sulfate, hydrochloride or the acetate of iron, cobalt, nickel or copper etc., and the metal ion weight concentration is 0.1%～10% in the aqueous solution;
Take out behind immersion 2～10h and dry, heat 2～10h in the air atmosphere under 373～673K temperature then, the slaine on the graphite felt is converted into metal oxide;
(3) then load there is the graphite felt of metal oxide at reducing atmosphere (H
2/ Ar gas) be warming up to 773～973K in and keep 1～6h, the metal oxide on the graphite felt is reduced to metal.Feed reactant gas then, reactant gas is selected from the mixture of a kind of and hydrogen in carbon monoxide, methane, ethane or the ethene, under 773～973K temperature, carry out the situ catalytic growth of carbon nano-fiber on graphite felt, growth time is 0.5～16h, obtains nano carbon fiber/graphite felt compound catalytic material at last.
Adopting the nano carbon fiber/graphite felt compound catalytic material of the inventive method preparation, have bigger density and very high machinery (resistance to compression and counter-bending) intensity, and have middle hole characteristic and very big external surface area, is a kind of novel carbonaceous catalysis material.
Description of drawings
Fig. 1 is the carbon nano-fiber of graphite felt fiber and growth in situ thereof.
Fig. 2 is the microscopic appearance of the carbon nano-fiber of growth in situ
The specific embodiment
Embodiment 1
Get 10 of polyacrylonitrile-radical graphite felt (the emerging carbon element in Shanghai Co., Ltd) that are of a size of 10*10*5 (mm), put into Muffle furnace, be warming up to 873K, insulation 4h.
Be immersed in after the taking-up in the nickel nitrate solution, the nickel weight content in the solution is 0.5%, and solvent is the mixture (volume ratio of ethanol and water is 1: 1) of ethanol and water, and soak time is 6h.
Take out the back centrifuge dripping, put into fume hood and dry naturally, put into 393K baking oven dried overnight then, again roasting 4h under 573K.There is the graphite felt of Raney nickel presoma to put into quartz tube furnace load, feeds H
2/ Ar (volume ratio is 1: 3) gaseous mixture 160ml/min is warming up to 873K, switches to H behind the insulation 3h
2/ C
2H
4(volume ratio is 1: 2) gaseous mixture 60ml/min carries out the situ catalytic growth of carbon nano-fiber, and growth time is 6h.Promptly get nano carbon fiber/graphite felt compound catalytic material after the cooling.
The weight that records carbon nano-fiber in the compound catalyze material is 5.3 times of graphite felt weight, and the density of compound catalyze material is 0.48g/cm
3(density of former graphite felt is 0.12g/cm
3), the malleation intensity during high compression 50% is 3.1MPa, three-point bending strength is 3.4Mpa.The average pore size that nitrogen low-temperature physics absorption method records is 10.0nm, and external surface area is 110m
2/ g, the micropore area is less than 1m
2/ g.
The electromicroscopic photograph of the carbon nano-fiber of graphite felt fiber and growth in situ thereof is seen Fig. 1.
The microscopic appearance electromicroscopic photograph of the carbon nano-fiber of growth in situ is seen Fig. 2.
The density of nano carbon fiber/graphite felt compound catalytic material can be by calculating behind the weight and volume of measuring the gained material; Malleation intensity and three-point bending strength adopt GB1041-79 (plastics compression test method) and GB1042-79 (plastics bend test method) to detect.
Embodiment 2
Get 20 of polyacrylonitrile-radical graphite felt that are of a size of φ 10*5 (mm), put into Muffle furnace, be warming up to 773K, insulation 4h.
Be immersed in after the taking-up in 1% nickel nitrate solution, solvent is the mixture (volume ratio of acetone and water is 1: 1) of acetone and water, and soak time is 6h.
Take out drying, put into fume hood and dry naturally, put into 393K baking oven dried overnight then, again roasting 4h under 573K.There is the graphite felt of Raney nickel presoma to put into quartz tube furnace load, feeds H
2/ Ar (volume ratio is 1: 4) gaseous mixture 160ml/min is warming up to 873K, switches to H behind the insulation 3h
2/ C
2H
4(volume ratio is 1: 2) gaseous mixture 60ml/min carries out the situ catalytic growth of carbon nano-fiber, and growth time is 8h.Promptly get nano carbon fiber/graphite felt compound catalytic material after the cooling.
The weight that records carbon nano-fiber in the compound catalyze material is 3.2 times of graphite felt weight, and the density of compound catalyze material is 0.38g/cm
3, the malleation intensity during high compression 50% is 1.4MPa.The average pore size that nitrogen low-temperature physics absorption method records is 6.8nm, and external surface area is 223m
2/ g.
Embodiment 3
Get 20 of polyacrylonitrile-radical graphite felt, be of a size of φ 10*5 (mm), put into Muffle furnace, be warming up to 973K, insulation 4h.
Be immersed in after the taking-up in the nickel nitrate solution, the nickel weight content in the solution is 1%, and soak time is 6h.
Take out drying, put into fume hood and dry naturally, put into 393K baking oven dried overnight then, again roasting 4h under 573K.
There is the graphite felt of Raney nickel presoma to put into quartz tube furnace load, feeds H
2/ Ar (volume ratio is 1: 3) gaseous mixture 160ml/min is warming up to 873K, switches to H behind the insulation 3h
2/ C
2H
4(volume ratio is 1: 2) gaseous mixture 60ml/min carries out the situ catalytic growth of carbon nano-fiber, and growth time is 3h.
Promptly get nano carbon fiber/graphite felt compound catalytic material after the cooling.The weight that records carbon nano-fiber in the compound catalyze material is 12.1 times of graphite felt weight, and the density of compound catalyze material is 0.28g/cm
3, the malleation intensity during high compression 40% is 3.1Mpa, three-point bending strength is 2.5Mpa.
Embodiment 4
Get the polyacrylonitrile-radical graphite felt several pieces, be of a size of φ 10*5 (mm), put into concentrated nitric acid solution and boil 0.5h.Filter and clean the back oven dry, be immersed in then in the nickel nitrate solution, the nickel weight content in the solution is 5%, and soak time is 10h.Take out drying, put into fume hood and dry naturally, put into 393K baking oven dried overnight then, again roasting 4h under 573K.There is the graphite felt of Raney nickel presoma to put into quartz tube furnace load, feeds H
2/ Ar (volume ratio is 1: 5) gaseous mixture 160ml/min is warming up to 873K, switches to H behind the insulation 3h
2/ C
2H
4(volume ratio is 1: 2) gaseous mixture 60ml/min carries out the situ catalytic growth of carbon nano-fiber, and growth time is 12h.Promptly get nano carbon fiber/graphite felt compound catalytic material after the cooling.The weight that records carbon nano-fiber in the compound catalyze material is 17.1 times of graphite felt weight.
Embodiment 5
Get the polyacrylonitrile-radical graphite felt several pieces, be of a size of φ 10*10 (mm), be immersed in the iron nitrate solution, the iron weight content in the solution is 5%, soak time is 10h.Take out drying, put into 393K baking oven dried overnight, again roasting 4h under 573K.There is the graphite felt of Raney nickel presoma to put into quartz tube furnace load, feeds H
2/ Ar (volume ratio is 1: 8) gaseous mixture 160ml/min is warming up to 873K, switches to H behind the insulation 3h
2/ CH
4(volume ratio is 1: 8) gaseous mixture 90ml/min carries out the situ catalytic growth of carbon nano-fiber, and growth time is 6h.Promptly get nano carbon fiber/graphite felt compound catalytic material after the cooling.The weight that records carbon nano-fiber in the compound catalyze material is 0.7 times of graphite felt weight.
Claims (7)
1. a nano carbon fiber/graphite felt compound catalytic material is characterized in that, is composited by the carbon nano-fiber of growth in situ on graphite felt and the graphite felt.
2. nano carbon fiber/graphite felt compound catalytic material according to claim 1 is characterized in that, is benchmark with graphite felt weight, and the weight of carbon nano-fiber is 0.5～30 times of graphite felt weight.
3. nano carbon fiber/graphite felt compound catalytic material according to claim 2 is characterized in that, is benchmark with graphite felt weight, and the weight of carbon nano-fiber is 3～10 times of graphite felt weight.
4. according to the preparation method of claim 1,2 or 3 described nano carbon fiber/graphite felt compound catalytic materials, it is characterized in that, comprise the steps:
(1) graphite felt is soaked or is boiled in salpeter solution 0.5～24h or under 573～1073K roasting 1～6h;
(2) graphite felt that step (1) is obtained is immersed in the aqueous solution that contains soluble metallic salt, adds ethanol, acetone, isopropyl alcohol or ethylene glycol in the aqueous solution;
Soluble metallic salt comprises nitrate, sulfate, hydrochloride or the acetate of iron, cobalt, nickel or copper etc., and the metal ion weight concentration is 0.1%～10% in the aqueous solution;
Take out behind immersion 2～10h and dry, heat 2～10h in the air atmosphere under 373～673K temperature then, the slaine on the graphite felt is converted into metal oxide;
(3) then load there is the graphite felt of metal oxide at reducing atmosphere (H
2/ Ar gas) be warming up to 773～973K in and keep 1～6h, metal oxide on the graphite felt is reduced to metal, feed reactant gas then, under 773～973K temperature, carry out the situ catalytic growth of carbon nano-fiber on graphite felt, growth time is 0.5～16h, obtains nano carbon fiber/graphite felt compound catalytic material at last.
5. method according to claim 4 is characterized in that, the mass concentration of salpeter solution is 10%～67%.
6. method according to claim 4 is characterized in that, in the aqueous solution, volume of organic solvent concentration is 10～60%.
7. method according to claim 4 is characterized in that, reactant gas is selected from the mixture of a kind of and hydrogen in carbon monoxide, methane, ethane or the ethene.
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| CN102123527A (en) * | 2011-01-10 | 2011-07-13 | 湖南金博复合材料科技有限公司 | Application and preparation method of carbon material heating body |
| CN101850249B (en) * | 2009-03-31 | 2011-12-28 | 华东理工大学 | Structured ruthenium catalyst and preparation method thereof |
| CN102887567A (en) * | 2012-10-11 | 2013-01-23 | 南开大学 | Method for modifying graphite felt material applied to electro-Fenton system |
| CN103050713A (en) * | 2011-10-17 | 2013-04-17 | 中国科学院大连化学物理研究所 | Electrode material modified by carbon nanofiber for vanadium redox flow battery and application thereof |
| CN103088648A (en) * | 2013-01-25 | 2013-05-08 | 中国科学院新疆生态与地理研究所 | Preparation method for carbon fiber material with composite nano structure |
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| CN107938323A (en) * | 2018-01-03 | 2018-04-20 | 北京北方国能科技有限公司 | A kind of graphene carbon fiber, its preparation method and its application |
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| EP1059266A3 (en) * | 1999-06-11 | 2000-12-20 | Iljin Nanotech Co., Ltd. | Mass synthesis method of high purity carbon nanotubes vertically aligned over large-size substrate using thermal chemical vapor deposition |
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| CN101850249B (en) * | 2009-03-31 | 2011-12-28 | 华东理工大学 | Structured ruthenium catalyst and preparation method thereof |
| CN102123527A (en) * | 2011-01-10 | 2011-07-13 | 湖南金博复合材料科技有限公司 | Application and preparation method of carbon material heating body |
| CN103050713A (en) * | 2011-10-17 | 2013-04-17 | 中国科学院大连化学物理研究所 | Electrode material modified by carbon nanofiber for vanadium redox flow battery and application thereof |
| CN102887567A (en) * | 2012-10-11 | 2013-01-23 | 南开大学 | Method for modifying graphite felt material applied to electro-Fenton system |
| CN102887567B (en) * | 2012-10-11 | 2014-01-15 | 南开大学 | Method for modifying graphite felt material applied to electro-Fenton system |
| CN103088648A (en) * | 2013-01-25 | 2013-05-08 | 中国科学院新疆生态与地理研究所 | Preparation method for carbon fiber material with composite nano structure |
| CN103088648B (en) * | 2013-01-25 | 2015-01-07 | 中国科学院新疆生态与地理研究所 | Preparation method for carbon fiber material with composite nano structure |
| CN107445641A (en) * | 2016-10-12 | 2017-12-08 | 平顺县西沟龙鼎新材料科技有限公司 | A kind of preparation method of carbon brake disc |
| CN107938323A (en) * | 2018-01-03 | 2018-04-20 | 北京北方国能科技有限公司 | A kind of graphene carbon fiber, its preparation method and its application |
| CN109534456A (en) * | 2018-11-12 | 2019-03-29 | 北京工业大学 | A kind of Co3O4/ graphite felt method for preparing composite electrode applied to anodic oxidation system |
| CN109534456B (en) * | 2018-11-12 | 2021-04-30 | 北京工业大学 | Preparation method of Co3O 4/graphite felt composite electrode applied to anodic oxidation system |
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