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Catalyst for preparing multi-walled carbon nanotubes, and preparation method and application thereof

A technology of multi-walled carbon nanotubes and catalysts, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxides/metal hydroxide catalysts, etc., can solve the problems of low carbon tube yield and poor crystallinity High, cumbersome preparation process and other issues, to achieve the effect of improving space utilization, large metal loading, and excellent spatial structure

Active Publication Date: 2020-04-07
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Chinese patent CN106458593A discloses a large-diameter, low-density carbon nanotube and a method for preparing the carbon nanotube. It uses an impregnation method to impregnate the active component on alumina, and the catalyst prepared by this method has a very small specific surface area. The growth space of multi-walled carbon nanotubes is limited, which is not conducive to the growth of carbon nanotubes; Chinese patent CN102145883A discloses a direct preparation of ultra-high-purity carbon nanotubes and its preparation method. The preparation process parameters of this method are complex to control and require Catalyst grains are dispersed on the surface of the inert carrier, and the space of the catalyst cannot be fully utilized; Chinese patent CN109665512A discloses a method for preparing multi-walled carbon nanotubes. The degree of graphitization of carbon nanotubes is not high (I_G / I_D=1.3)
In 2005, some scientists reported the preparation of Mg by urea combustion method 0.90 Fe x co y O(x+y=0.1) solid solution (Coquay P.; Peigney A.; De Grave E.; Flahaut E.; Vandenberghe R.E.; Laurent C., Fe / Co Alloys for the Catalytic Chemical Vapor Deposition Synthesis of Single-and Double- Walled Carbon Nanotubes (CNTs). 1. The CNT-Fe / Co-MgO System. The Journal of Physical Chemistry B [J] 2005, 109 (38): 17813-17824.), the specific surface area of ​​the resulting catalyst is small (less than 52m2 / g), and the preparation process of this method has a small amount of preparation, it is not easy to control the reaction rate, and it is extremely prone to explosion
In 2012, a study reported the preparation of (Al 2 -xFe x o 3 )-(y)ZrO 2 (x=0.017, 0.034 and 0.17 and y=0.15) ceramic nanocomposite catalysts (Beitollahi A.; Pilehvari S.; Sani M.F.; Moradi H.; Akbamejad M., In situ growth of carbon nanotubes in alumina-zirconiananocomposite matrix prepared by solution combustion method.CeramicsInternational[J].2012,38(4):3273-3280.), yet the catalyst metal lacks a strong interaction with the support, and the resulting carbon tube yield is lower than 23%, and I_G / I_D does not exceed 3
In 2018, a study reported the preparation of catalysts by sol-gel method (Kim P.; Lee C.J., The ReductionTemperature Effect of Fe-Co / MgO Catalyst on Characteristics of Multi-WalledCarbon Nanotubes.Catalysts[J].2018, 8(9 ).), the catalyst will expand violently and emit a large amount of heat in the reaction process, which will affect the reaction equipment and reaction safety, and is not suitable for large-scale reactions; not tall

Method used

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  • Catalyst for preparing multi-walled carbon nanotubes, and preparation method and application thereof
  • Catalyst for preparing multi-walled carbon nanotubes, and preparation method and application thereof
  • Catalyst for preparing multi-walled carbon nanotubes, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1A-30F

[0034] Example 1A-30Fe 15 -Mo / MgO catalyst

[0035] Dissolve 0.8761g of ammonium molybdate and 23.8386g of citric acid monohydrate in 15mL of deionized water, add 1.65mL of nitric acid and stir well, add 30.0715g of ferric nitrate nonahydrate and stir well, add 0.5g of urea and stir well, then add 10g of light oxidation Magnesium, the resulting mixture was continuously stirred for 180 minutes, then stirred and evaporated to dryness at 80°C for 300 minutes, the obtained solid was dried and foamed at 150°C for 3 hours, and then placed in a blast drying oven at 110°C to dry overnight, and the dried solid was ground into powder In a muffle furnace, the temperature is raised to 500°C for 180min at 2°C / min to obtain a composition of 30mol% Fe 15 -Mo / MgO catalyst, and recorded as A-30Fe 15 -Mo / MgO. The characterization results of the catalyst show that the MgO particle size is about 6.4nm, the pore structure is 0.51-1.80um, and the average pore diameter is 1.77μm. See Table 1 for ...

Embodiment 2B-20

[0037] Example 2B-20Fe 15 -Mo / MgO catalyst

[0038] Add 0.4764g of molybdenum oxide and 23.8386g of citric acid monohydrate to 15mL of deionized water, add 12.7238g of magnesium nitrate hexahydrate and stir evenly, add 20.0676g of ferric nitrate nonahydrate and stir evenly, add 1mL of concentrated ammonia water and stir evenly, then add 8g of light Magnesium oxide, the resulting mixture was stirred for 30 minutes, then stirred and evaporated to dryness at 120°C for 30 minutes, the obtained solid was dried and foamed at 80°C for 12 hours, and then placed in a blast drying oven at 110°C to dry overnight, and the dried solid was ground into Powder, in a muffle furnace at 2°C / min to 450°C and roasted for 300min to obtain a composition of 20mol% Fe 15 -Mo / MgO catalyst, and recorded as B-20Fe 15 -Mo / MgO. The particle size of the catalyst MgO is about 13.8nm, the pore structure is 0.62-1.67μm, and the average pore size is 0.95μm. See Table 1 for other characterization results.

...

Embodiment 3

[0040] Example 3C-10Fe 20 - Mo / MgO catalyst

[0041] Dissolve 0.4046g of molybdenum acetylacetonate and 27.0145g of citric acid monohydrate in 15mL of deionized water, add 12.7238g of magnesium nitrate hexahydrate and stir evenly, add 15.0357g of iron nitrate nonahydrate and stir evenly, add 1.0g of glycine (aminoacetic acid) and stir After uniformity, 31.3290g of basic magnesium carbonate was added, and the resulting mixture was stirred for 30 minutes, then stirred and evaporated to dryness at 120°C for 30 minutes, and the obtained solid was dried and foamed at 80°C for 12 hours, and then placed in a blast drying oven at 110°C to dry overnight. Grind the dried solid into powder, heat up to 600°C for 180min in a muffle furnace at 2°C / min to obtain a composition of 10mol% Fe 20 -Mo / MgO catalyst, and denoted as C-10Fe 20 -Mo / MgO. The particle size of catalyst MgO is about 15.8nm, the pore structure is 0.52-1.63μm, and the average pore size is 0.98μm. See Table 1 for other cha...

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Abstract

The invention discloses a catalyst for preparing multi-walled carbon nanotubes, and a preparation method and an application thereof. The catalyst adopts MgO as a carrier, metal Fe, Co or Ni as an active component and metal Mo as an auxiliary agent, and the chemical general formula of the catalyst can be expressed as xMa-Mob / MgO, wherein x is the molar percentage of M in MgO, M is one of Fe, Co andNi, and a:b represents a molar ratio of M to Mo. The catalyst can form a foam-like porous loose structure, and has the advantages of high loading capacity, large specific surface area and favorable activity, so a sufficient space is provided for the growth of carbon nanotubes; and the high-quality carbon nanotubes can be prepared. The catalyst has the advantages of simple preparation method, safeand feasible preparation process, good large-scale preparation activity, large specific surface area (up to 154 m<2> / g), excellent space structure and the like. The high-quality carbon nanotubes canbe prepared by using the catalyst, I_G / I_D can reach 17, the average diameter is 8.7 nm, and the carbon content of crude carbon nanotubes exceeds 92%.

Description

technical field [0001] The invention belongs to the technical field of carbon nanotube preparation, and in particular relates to a catalyst for preparing multi-walled carbon nanotubes, a preparation method and application thereof. Background technique [0002] Multi-walled carbon nanotube (MWCNT) was first prepared by Japanese researcher Ijima in 1991. It can be regarded as a seamless tubular material formed by curling graphene sheets. Multi-walled carbon nanotubes have many excellent properties, such as good electrical conductivity, excellent thermal conductivity, ultra-high strength and tensile strength, large specific surface area and efficient catalytic performance, etc., which make it in energy, chemical It has broad application prospects in fields such as physical sensors, catalytic materials and composite materials. [0003] After nearly 30 years of development, the preparation of multi-walled carbon nanotubes has developed rapidly. The main preparation methods are ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/881B01J23/882B01J35/10C01B32/162
CPCB01J23/8872C01B32/162B01J35/615
Inventor 陈秉辉吴钊男郑进保曹志凯谢建榕张诺伟
Owner XIAMEN UNIV
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