CN110586155A - Application of carbon nano tube embedded metal particle catalyst in CO selective oxidation purification reaction in hydrogen-rich gas - Google Patents
Application of carbon nano tube embedded metal particle catalyst in CO selective oxidation purification reaction in hydrogen-rich gas Download PDFInfo
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- 238000006243 chemical reaction Methods 0.000 title claims abstract description 113
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 107
- 239000002041 carbon nanotube Substances 0.000 title claims abstract description 87
- 229910021393 carbon nanotube Inorganic materials 0.000 title claims abstract description 86
- 239000003054 catalyst Substances 0.000 title claims abstract description 83
- 239000007789 gas Substances 0.000 title claims abstract description 36
- 239000002923 metal particle Substances 0.000 title claims abstract description 33
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 239000001257 hydrogen Substances 0.000 title claims abstract description 10
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 10
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 10
- 238000000746 purification Methods 0.000 title claims abstract description 9
- 230000003647 oxidation Effects 0.000 title claims abstract description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 56
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 39
- 229910052751 metal Inorganic materials 0.000 claims abstract description 17
- 239000002184 metal Substances 0.000 claims abstract description 17
- 238000011068 loading method Methods 0.000 claims abstract description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000002082 metal nanoparticle Substances 0.000 claims abstract description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052707 ruthenium Inorganic materials 0.000 claims abstract description 5
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 3
- 239000010941 cobalt Substances 0.000 claims abstract description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052737 gold Inorganic materials 0.000 claims abstract description 3
- 239000010931 gold Substances 0.000 claims abstract description 3
- 229910052741 iridium Inorganic materials 0.000 claims abstract description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000002048 multi walled nanotube Substances 0.000 claims abstract description 3
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 3
- 229910052763 palladium Inorganic materials 0.000 claims abstract description 3
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 3
- 239000002109 single walled nanotube Substances 0.000 claims abstract description 3
- 239000002245 particle Substances 0.000 claims description 45
- 239000006004 Quartz sand Substances 0.000 claims description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 25
- 239000000243 solution Substances 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 238000003756 stirring Methods 0.000 claims description 17
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 15
- 238000001035 drying Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 238000000502 dialysis Methods 0.000 claims description 12
- 229910021645 metal ion Inorganic materials 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 238000010306 acid treatment Methods 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 8
- 230000007935 neutral effect Effects 0.000 claims description 8
- 238000000967 suction filtration Methods 0.000 claims description 8
- 238000005406 washing Methods 0.000 claims description 8
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 7
- 239000008367 deionised water Substances 0.000 claims description 7
- 229910021641 deionized water Inorganic materials 0.000 claims description 7
- 229910017604 nitric acid Inorganic materials 0.000 claims description 7
- 238000010992 reflux Methods 0.000 claims description 7
- 239000000706 filtrate Substances 0.000 claims description 5
- 239000002002 slurry Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 4
- 239000006228 supernatant Substances 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 6
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- 238000001514 detection method Methods 0.000 description 22
- 238000004817 gas chromatography Methods 0.000 description 22
- 229910001873 dinitrogen Inorganic materials 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 15
- 238000011049 filling Methods 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 8
- 239000000945 filler Substances 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229910021389 graphene Inorganic materials 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
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- 238000009826 distribution Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- -1 metal complex ions Chemical class 0.000 description 2
- 239000002086 nanomaterial Substances 0.000 description 2
- 239000011146 organic particle Substances 0.000 description 2
- 229910021639 Iridium tetrachloride Inorganic materials 0.000 description 1
- 229910019029 PtCl4 Inorganic materials 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 229910003481 amorphous carbon Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007847 structural defect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- FBEIPJNQGITEBL-UHFFFAOYSA-J tetrachloroplatinum Chemical compound Cl[Pt](Cl)(Cl)Cl FBEIPJNQGITEBL-UHFFFAOYSA-J 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
-
- B01J35/40—
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/50—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification
- C01B3/56—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification by contacting with solids; Regeneration of used solids
- C01B3/58—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification by contacting with solids; Regeneration of used solids including a catalytic reaction
- C01B3/583—Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification by contacting with solids; Regeneration of used solids including a catalytic reaction the reaction being the selective oxidation of carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/04—Integrated processes for the production of hydrogen or synthesis gas containing a purification step for the hydrogen or the synthesis gas
- C01B2203/0435—Catalytic purification
- C01B2203/044—Selective oxidation of carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
- C01B2203/1047—Group VIII metal catalysts
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
- C01B2203/1047—Group VIII metal catalysts
- C01B2203/1052—Nickel or cobalt catalysts
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
- C01B2203/1047—Group VIII metal catalysts
- C01B2203/1052—Nickel or cobalt catalysts
- C01B2203/1058—Nickel catalysts
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
- C01B2203/1047—Group VIII metal catalysts
- C01B2203/1064—Platinum group metal catalysts
- C01B2203/107—Platinum catalysts
Abstract
The application of the catalyst with metal particles embedded in the carbon nano tube in CO selective oxidation purification reaction in hydrogen-rich gas is characterized in that: the catalyst consists of a carbon nano tube, nitrogen-doped carbon quantum dots and metal nano particles, wherein the carbon nano tube is a single-walled or multi-walled carbon nano tube with an opening, the nitrogen-doped carbon quantum dots are loaded on the outer wall of the carbon nano tube, and the metal nano particles are embedded in the inner wall of the carbon nano tube; the metal is one of palladium, platinum, gold, ruthenium, iridium, nickel and cobalt; the size of the nitrogen-doped carbon quantum dot is not more than 10nm, and the nitrogen content is 0.1-8.0 wt%; in the catalyst with metal particles embedded in the carbon nano tube, the loading capacity of nitrogen-doped carbon quantum dots is 0.5-8.0 wt%, and the loading capacity of metal is 0.1-10.0 wt%. The catalyst provided by the invention realizes CO selective oxidation reaction in a hydrogen-rich system under the synergistic effect of the carbon quantum dots, the embedded metal particles and the confinement effect of the carbon nano tube, maintains high conversion rate and high stability at high space velocity, and has high catalytic efficiency and long service life.
Description
(I) technical field
The invention relates to application of a carbon nano tube embedded metal particle catalyst in CO selective oxidation purification reaction in hydrogen-rich gas.
(II) technical background
Carbon nanotubes have structural defects, curved surfaces, unique lumen structures, and electrical conductivity properties, and are excellent catalytic materials. Based on the collision theory of chemical reaction, the reaction space in the tube is obviously reduced, and the unique interaction of reactants and products with the inner wall of the carbon nano tube can influence the progress of the chemical reaction. Santis et al have learned through theoretical calculations that when the chemical reaction is confined to a small pore size, the reaction kinetics change significantly and the reaction rate can jump by orders of magnitude. Lu et al calculated the mechanism of the limited-domain reaction in carbon nanotubes using DFT theory, found that after the reaction limited-domain was inside the carbon nanotubes, the barrier affecting the reaction progress was significantly reduced, and the reactivity of the reactants in the tubes was enhanced with the reduction of the tube diameter of the carbon nanotubes. Therefore, the catalyst with the carbon nano tubes embedded with the metal particles can be used for preparing ethanol by converting synthesis gas, performing Fischer-Tropsch reaction, performing benzene hydrogenation reaction and performing NH reaction3The catalyst shows excellent catalytic performance in the decomposition reaction.
The preparation method of the prior metal catalyst loaded in the tube mainly comprises the following steps: in-situ filling methods, gas phase filling methods, and liquid phase filling methods. The in-situ filling method adopts the means of an electric arc method, a microwave method and the like to generate metal or compound in situ in the cavity channel and the shell layer of the carbon nano tube in the process of preparing the carbon nano tube. Generally, the in-situ filling method can fill a plurality of metals with higher melting points and higher surface tension, but the in-situ filling method has lower filling yield, and some metal carbides or metal particles are assembled into the carbon nanotube shell during the filling process. The gas phase filling method is a method of performing a high-temperature reaction in a gas phase. That is, the carbon nanotubes are mixed with the filler under a certain pressure and temperature, and the filler is vaporized by heating and introduced into the carbon nanotubes. The gas phase method has the advantages that only gas capable of reacting with the carbon nano tube is needed in the reaction, more reagents are not needed, the environment is not polluted, and other substances are not introduced into the system; the method has the disadvantages that the carbon nano tube has low opening rate, needs high temperature of 500-1000 ℃, is difficult to control proper reaction time and temperature, and is not easy to fill because amorphous carbon is accumulated in a tube cavity. The liquid phase filling method mixes and grinds the filler and the carbon nano tube to ensure that the filler and the carbon nano tube are fully contacted, then the temperature is raised to be higher than the melting point of the filler, and the melted filler enters the interior of the carbon nano tube under the capillary action. The filling of salts such as metal halides and oxides is usually carried out by melting the filling.
However, the existing preparation method of the metal particles embedded in the carbon nano tube has the defects of complex process, difficult regulation and control of the deposition process in the metal particles, low proportion in the metal particle tube, low metal utilization rate and the like. The problems of low activity, low selectivity, undesirable purification effect and the like are shown in the selective oxidation purification reaction of CO in the hydrogen-rich gas.
Disclosure of the invention
The invention aims to provide application of a carbon nano tube embedded metal particle catalyst with carbon quantum dots loaded outside a tube and metal particles embedded inside the tube in CO selective oxidation purification reaction in hydrogen-rich gas, and the catalyst realizes high conversion rate, high selectivity and high stability, high catalytic efficiency and long service life of the catalyst under the synergistic effect of the confinement effect of the carbon quantum dots, the embedded metal particles and the carbon nano tube.
In order to achieve the purpose, the invention adopts the following technical scheme:
the invention provides an application of a carbon nanotube embedded metal particle catalyst in CO selective oxidation purification reaction in hydrogen-rich gas, wherein the catalyst consists of a carbon nanotube, a nitrogen-doped carbon quantum dot and a metal nanoparticle, the carbon nanotube is a single-walled or multi-walled carbon nanotube with an opening, the nitrogen-doped carbon quantum dot is distributed on the outer wall of the carbon nanotube in a loading manner, and the metal nanoparticle is embedded on the inner wall of the carbon nanotube; the metal is one of palladium, platinum, gold, ruthenium, iridium, nickel and cobalt; the size of the nitrogen-doped carbon quantum dot is not more than 10nm, and the nitrogen content is 0.1-8.0 wt%; in the catalyst with metal particles embedded in the carbon nano tube, the loading capacity of nitrogen-doped carbon quantum dots (the mass ratio of the carbon quantum dots to the carbon nano tube) is 0.5-8.0 wt%, and the loading capacity of metal is 0.1-10.0 wt%.
Preferably, in the carbon nanotube embedded metal particle catalyst, the loading amount of nitrogen-doped carbon quantum dots is 0.5-5.0 wt%. Preferably, the loading of metal in the catalyst is 0.5 to 5.0 wt%.
Preferably, the size of the nitrogen-doped carbon quantum dots is 0.5-2.5 nm.
Preferably, the carbon nanotube embedded metal particle catalyst can be prepared by the following method:
1) placing the carbon nano tube in concentrated nitric acid (65-68 wt%) for heating reflux treatment, cooling to room temperature after the reflux treatment is finished, washing with water until the filtrate is neutral, and drying to obtain the carbon nano tube subjected to acid treatment; because the freshly prepared carbon nano tube is a tube which grows out on metal particles and is usually closed, in order to utilize the space in the tube and remove the metal particles of the long carbon tube, concentrated nitric acid is adopted for pretreatment;
2) preparing a nitrogen-doped carbon quantum dot solution and the carbon nano tube subjected to acid treatment obtained in the step 1) into a dispersion liquid, fully stirring to enable the carbon quantum dots to be loaded on the outer wall of the carbon nano tube, and performing suction filtration and drying to obtain the carbon nano tube loaded with the carbon dots;
3) preparing the carbon nano tube loaded with the carbon dots obtained in the step 2) and deionized water into slurry, adding aqueous solution containing metal ions under the stirring state, forming complex anions by the metal ions and chloride ions in the aqueous solution, fully stirring, performing suction filtration, washing until the pH value of filtrate is neutral, and drying to obtain the carbon nano tube embedded metal particle catalyst.
According to the preparation method, the nitrogen-doped carbon quantum dots and the carbon nano tubes are adsorbed on the outer walls of the carbon nano tubes through pi-pi conjugation so as to be converted into excellent electron-donating centers, and then metal complex ions with negative charges are induced to spontaneously enter the tubes and deposit on the inner walls by utilizing the electron-donating characteristics of the nitrogen-doped carbon quantum dots, wherein the electrical enrichment property of nitrogen atoms is favorable for the metal ions to enter the tubes and be loaded on the inner walls of the tubes, so that the small-particle-size and uniform distribution of metal active components in the carbon nano tubes is realized.
In the step 1), the nitric acid treatment is a conventional treatment method for opening the carbon tube and removing residual metal. Preferably, in the acid treatment process of the carbon nano tube in the step 1), the ratio of the carbon nano tube to the nitric acid is 1-10 g: 20-100ml, the treatment temperature is 45-95 ℃, and the condensation reflux is carried out for 2-15 h. Preferably, the drying conditions are: drying at 50-100 deg.C for 1-10 hr. Preferably, the diameter distribution of the carbon nanotubes is 20-40nm, and the specific surface area is more than 150m2/g。
In the present invention, the nitrogen-doped carbon quantum dots can be prepared by referring to the prior art. Preferably, the nitrogen-doped carbon quantum dots are prepared by using citric acid and ethylenediamine as raw materials and utilizing esterification reaction or amidation reaction of carboxyl and amino under the assistance of microwaves to generate the nitrogen-doped carbon dots, and the electrical enrichment of heteroatoms is favorable for metal ions to enter the tube and be loaded on the inner wall of the tube. The microwave method is simple to operate and has high nitrogen doping content. The specific process is as follows: adding deionized water, citric acid and ethylenediamine into a crucible at a ratio of 1-15 mL: 0.5-5.0 g: 0.01-1.0mL, and mechanically stirring until the mixture is uniformly mixed; then placing the solution in a microwave oven with the power of 300-1500W and the heating time of 0.5-10min to obtain a light yellow carbon quantum dot solution; then, centrifugal treatment is carried out (organic matter particles which are not completely carbonized are removed) under the condition that the rotating speed is 20000r/min, supernatant is transferred into a two-layer dialysis bag with the molecular weight of 100-10000 Dalton for dialysis treatment, the carbon dot solution in the middle of the two layers is the carbon dot solution, and finally, the solution is concentrated to the concentration of 0.5-25.0mg/L under the condition of shading low temperature. As a further preference, the cut-off molecular weight size of the dialysis bag is 100-.
Step 2) of the present invention is preferably carried out as follows: and feeding the nitrogen-doped carbon quantum dot solution and the carbon nano tube subjected to acid treatment according to the loading capacity of the nitrogen-doped carbon quantum dots, stirring for 10-60min, and drying the filtered solid particles in a vacuum oven at the temperature of 50-100 ℃ for 2-15h to obtain the carbon nano tube loaded with the carbon dots.
Step 3) of the present invention is preferably carried out as follows: preparing the carbon nano tube loaded with the carbon dots obtained in the step 2) into slurry according to the feeding ratio of the carbon nano tube loaded with the carbon dots to water of 1 g: 5-35ml, adding the corresponding aqueous solution containing the metal ions according to the metal loading capacity at the temperature of 5-40 ℃ under the stirring state, wherein the dropping speed of the aqueous solution containing the metal ions is 1d/1-10s, continuously stirring for 2-6h after dropping, performing suction filtration, washing until the pH value is neutral, and drying for 3-15h at the temperature of 50-100 ℃ to obtain the catalyst.
Preferably, the application method comprises the following steps:
the catalyst is evenly mixed with quartz sand particles, the granularity of the quartz sand is 0.5-2mm, the quartz sand particles are placed in a fixed bed reactor (the inner diameter is 6mm), the reaction pressure is 0.1MPa, the CO content is 1-5mol percent, and O is2Content 1 mol%, H2The content is 40-80 mol%, the rest nitrogen is complemented, and the space velocity is 1000--1gcat -1The reaction temperature is 40-200 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD.
Compared with the prior art, the invention has the beneficial effects that:
1) in the catalyst with embedded metal particles in the carbon nano tube, the catalyst structure is designed to load nitrogen-doped carbon quantum dots outside the tube, the metal particles are embedded in the tube, and the catalyst generates specific catalytic characteristics due to the electron donating characteristics of the nitrogen-doped carbon quantum dots, the carbon tube to the metal particles and the confinement effect of the carbon tube to reactant molecules. Under the synergistic effect of the carbon quantum dots, the embedded metal particles and the confinement effect of the carbon nano tubes, the high conversion rate and the high stability are kept at high airspeed in the CO selective oxidation reaction in a hydrogen-rich system, the catalytic efficiency is high, and the service life of the catalyst is long.
2) In the preparation method of the catalyst, metal ions of anions are driven to the inner wall of the carbon tube through the electrostatic action by virtue of the electron-rich characteristic of the carbon quantum dots loaded on the outer wall of the carbon tube, so that the metal utilization rate is remarkably improved. The method is simple, convenient and easy to control, and has low cost.
(IV) description of the drawings
A and b in fig. 1 are electron micrographs of the catalysts prepared in comparative example 1 and example 1, respectively.
Fig. 2 is a graph showing the percentage of metal particles in carbon nanotubes in the catalysts prepared in example 1, comparative example 1, and comparative example 3, where 1 is comparative example 1; 2 is comparative example 3; example 3 data from randomly selected 500 particles (TEM characterization) are obtained for example 1.
(V) detailed description of the preferred embodiments
The technical solution of the present invention is specifically described below with specific examples, but the scope of the present invention is not limited thereto:
the carbon tubes used in the examples were obtained from Nanjing Xiancheng nanomaterial science and technology Co., Ltd, and the graphene was obtained from Chengdu organic chemistry Co., Ltd, academy of sciences, China.
Example 1
1) Deionized water, citric acid and ethylenediamine are added into a crucible, the dosage is respectively 10 mL: 2.5 g: 0.5mL, and the materials are mechanically stirred until the materials are uniformly mixed. Then placing the mixture in a microwave oven with the power of 1000W and the heating time of 2min to obtain a light yellow carbon quantum dot solution. Then carrying out centrifugal treatment (removing organic particles which are not completely carbonized) at the rotation speed of 20000r/min, transferring the supernatant into a two-layer dialysis bag with the molecular weight of 200-1000 Dalton for dialysis treatment, wherein the carbon dot solution in the middle of the two layers is the required carbon dot solution, and finally concentrating under the condition of shading low temperature until the concentration is 5.0 mg/L. The detection proves that the nitrogen content in the carbon dots is 5 percent.
2) Weighing 10g of carbon nano-tube (diameter distribution is 20-40nm, specific surface area is more than 150 m)2Put into a round-bottom flask, then concentrated nitric acid (65-68 wt%) is measured and added into the flask, the ratio of the carbon nano tube to the nitric acid is 5 g: 50ml, and then the flask is put into a hydrothermal pot for heating and refluxing for 5 hours at 90 ℃. And after the reflux is finished, taking out the flask, cooling to a room temperature state, transferring to a funnel, adding deionized water, continuously washing, performing suction filtration until the filtrate is neutral, and then putting the filter cake into an oven to dry for 10 hours at the temperature of 80 ℃. Obtaining the carbon nano tube treated by acid for standby.
3) Preparing a mixed solution of the carbon quantum dot solution prepared in the step 1) and the carbon nano tube treated by acid, wherein the mass ratio of the carbon dots to the carbon nano tube is 5.0 wt%, then placing the solution on a magnetic stirrer for stirring, carrying out suction filtration after 30min, and then placing the obtained solid particles into a vacuum oven for drying for 5h at 100 ℃ to obtain the carbon nano tube loaded with the carbon dots.
4) Preparing the solid obtained in the step 3) and deionized water into slurry, wherein the ratio of the solid to the water is 1g to 5ml, and ruthenium ions [ RuCl ] with the corresponding load of 5.0 wt% are added under the stirring state at 40 DEG C4]2-The dropping rate of the aqueous solution of (4) was 1 d/5S. Stirring for 6 hours, carrying out suction filtration, washing until the pH value is neutral, and drying for 15 hours at 100 ℃ to obtain the catalyst.
Examples 2 to 15
The catalyst was prepared according to example 1, with specific parameters as shown in Table 1.
TABLE 1
Note: metal ion form in the impregnation: [ PdCl4]2-，[PtCl4]2-，[IrCl4]2-，[AuCl4]2-，[NiCl4]2-，[CoCl4]2-，[RuCl4]2-。
Comparative example 1
The preparation method is the same as that of example 1 except that carbon quantum dots are not added.
Comparative example 2
Graphene was used instead of carbon nanotubes, and the other preparation methods were the same as in example 1. Graphene is a polymer made of carbon atoms in sp2The hybrid tracks form hexagonal honeycomb lattice two-dimensional carbon nano-materials without tubular structures.
Comparative example 3
1) Citric acid and ethanol are taken in a beaker, the proportion is 0.5 g: 15mL, and the mixture is mechanically stirred until the mixture is uniformly mixed. Then transferred to a hydrothermal kettle, hydrothermal for 15 hours at 160 ℃, and then naturally cooled. Then, centrifugal treatment is carried out (organic particles which are not completely carbonized are removed) under the condition that the rotating speed is 20000r/min, supernatant is transferred into a two-layer dialysis bag with the molecular weight of 200-1000 Dalton for dialysis treatment, the carbon dot solution in the middle of the two layers is the required carbon dot solution (the carbon dot does not contain heteroatoms), and finally concentration is carried out at low temperature under shading until the concentration is 5.0 mg/L. The carbon dots prepared do not contain heteroatom N.
Steps 2) to 4) the catalyst was obtained in the same manner as in example 1.
Comparative example 4
Using the literature Catalysis today, 2011, 164: 74-79 reports 5 wt.% Ru/CNTs catalyst of metal particles deposited in the carbon tube prepared by the preparation method.
Comparative example 4
The dialysis was performed using a dialysis membrane having a molecular weight of 4000-6000 daltons, and the rest of the preparation was the same as in example 1.
Example 16
The catalyst of example 1 is uniformly mixed with quartz sand particles with the granularity of 0.5-2mm, and the mixture is placed in a fixed bed reactor (the inner diameter is 6mm) with the reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 17
The catalyst of example 2 is uniformly mixed with quartz sand particles with the granularity of 0.5-2mm, and the mixture is placed in a fixed bed reactor (the inner diameter is 6mm) with the reaction pressure of 0.1MPa and CO/O2/H25/1/50 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 200 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 18
The catalyst of example 3 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, and placed in a fixed bed reactor (inner diameter 6mm)Reaction pressure 0.1MPa, CO/O2/H22/1/45 (mol%), nitrogen gas and space velocity 10000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 19
The catalyst of example 4 is mixed with quartz sand particles with a particle size of 0.5-2mm, and the mixture is placed in a fixed bed reactor (inner diameter 6mm) with a reaction pressure of 0.1MPa and CO/O2/H23/1/80 (mol%), nitrogen gas and space velocity 1000ml h-1 gcat -1The reaction temperature was 50 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 20
The catalyst of example 5 and quartz sand particles with the granularity of 0.5-2mm are uniformly mixed, and the mixture is placed in a fixed bed reactor (the inner diameter is 6mm) with the reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen balance, space velocity 5000ml h-1 gcat -1The reaction temperature was 40 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 21
The catalyst of example 6 and quartz sand particles with the granularity of 0.5-2mm are uniformly mixed, and the mixture is placed in a fixed bed reactor (the inner diameter is 6mm) with the reaction pressure of 0.1MPa and CO/O2/H21/1/70 (mol%), nitrogen balance, space velocity 5000ml h-1 gcat -1The reaction temperature was 60 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 22
The catalyst of example 7 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H22/1/45 (mol%), nitrogen balance, space velocity 30000ml h-1 gcat -1The reaction temperature was 200 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 23
The catalyst of example 8 and quartz sand particles with a particle size of 0.5-2mm were mixed uniformly in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/60 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 180 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 24
The catalyst of example 9 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/50 (mol%), nitrogen gas and space velocity 20000ml h-1 gcat -1The reaction temperature was 200 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 25
The catalyst of example 10 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H24/1/45 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Reaction ofThe catalyst was not treated specifically before. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 26
The catalyst of example 11 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 27
The catalyst of example 12 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/45 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 28
The catalyst of example 13 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/50 (mol%), nitrogen balance, space velocity 40000ml h-1 gcat -1The reaction temperature was 50 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 29
The catalyst of example 14 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, and placed in a fixed bed reactor (1)Inner diameter 6mm), reaction pressure 0.1MPa, CO/O2/H21/1/45 (mol%), nitrogen gas and space velocity 20000ml h-1 gcat -1The reaction temperature was 80 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 30
The catalyst of example 15 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 10000ml h-1 gcat -1The reaction temperature was 100 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Example 31
The catalyst of comparative example 1 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 43 percent, and CO is generated2The selectivity of (2) was 85%.
Example 32
The catalyst of comparative example 2 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 37 percent, and CO is generated2Selectivity of (2) was 74%.
Example 33
The catalyst of comparative example 3 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 90 percent, and CO is generated2Selectivity of (3) was 79%.
Example 34
The catalyst of comparative example 4 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 81 percent, and CO is generated2The selectivity of (2) was 80%.
Example 35
The catalyst of comparative example 5 was uniformly mixed with quartz sand particles having a particle size of 0.5 to 2mm, placed in a fixed bed reactor (inner diameter 6mm) at a reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature was 150 ℃. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 10 hours, the detection shows that the conversion rate of CO is 95 percent, and CO is generated2The selectivity of (2) was 98%.
Example 24
The catalyst of example 1 is uniformly mixed with quartz sand particles with the granularity of 0.5-2mm, and the mixture is placed in a fixed bed reactor (the inner diameter is 6mm) with the reaction pressure of 0.1MPa and CO/O2/H21/1/40 (mol%), nitrogen gas and space velocity 50000ml h-1 gcat -1The reaction temperature is 150 DEG C. Before the reaction, the catalyst is not specially treated. The tail gas is detected by gas chromatography with TCD. After 150 hours, the detection shows that the conversion rate of CO is 100 percent, and CO is generated2The selectivity of (2) is 100%.
Claims (8)
1. The application of the catalyst with metal particles embedded in the carbon nano tube in CO selective oxidation purification reaction in hydrogen-rich gas is characterized in that: the catalyst consists of a carbon nano tube, nitrogen-doped carbon quantum dots and metal nano particles, wherein the carbon nano tube is a single-walled or multi-walled carbon nano tube with an opening, the nitrogen-doped carbon quantum dots are loaded on the outer wall of the carbon nano tube, and the metal nano particles are embedded in the inner wall of the carbon nano tube; the metal is one of palladium, platinum, gold, ruthenium, iridium, nickel and cobalt; the size of the nitrogen-doped carbon quantum dot is not more than 10nm, and the nitrogen content is 0.1-8.0 wt%; in the catalyst with metal particles embedded in the carbon nano tube, the loading capacity of nitrogen-doped carbon quantum dots is 0.5-8.0 wt%, and the loading capacity of metal is 0.1-10.0 wt%.
2. The use of claim 1, wherein: the size of the nitrogen-doped carbon quantum dots is 0.5-2.5 nm.
3. The use of claim 1, wherein: the carbon nano tube embedded metal particle catalyst is prepared by the following method:
1) placing the carbon nano tube in concentrated nitric acid, heating and refluxing, cooling to room temperature after the heating and refluxing treatment, washing with water until filtrate is neutral, and drying to obtain the carbon nano tube subjected to acid treatment;
2) preparing a nitrogen-doped carbon quantum dot solution and the carbon nano tube subjected to acid treatment obtained in the step 1) into a dispersion liquid, fully stirring to enable the carbon quantum dots to be loaded on the outer wall of the carbon nano tube, and performing suction filtration and drying to obtain the carbon nano tube loaded with the carbon dots;
3) preparing the carbon nano tube loaded with the carbon dots obtained in the step 2) and deionized water into slurry, adding aqueous solution containing metal ions under the stirring state, forming complex anions by the metal ions and chloride ions in the aqueous solution, fully stirring, performing suction filtration, washing until the pH value of filtrate is neutral, and drying to obtain the carbon nano tube embedded metal particle catalyst.
4. Use according to claim 3, characterized in that: the nitrogen-doped carbon quantum dot is prepared according to the following method: adding deionized water, citric acid and ethylenediamine into a crucible at a ratio of 1-15 mL: 0.5-5.0 g: 0.01-1.0mL, mechanically stirring until the mixture is uniformly mixed; then placing the solution in a microwave oven with the power of 300-1500W and the heating time of 0.5-10min to obtain a light yellow carbon quantum dot solution; then centrifugal treatment is carried out under the condition that the rotating speed is 20000r/min, supernatant is transferred into a two-layer dialysis bag with the molecular weight of 100-10000 Dalton for dialysis treatment, the carbon dot solution between the two layers is the carbon dot solution, and finally concentration is carried out under the shading low temperature until the concentration is 0.5-25.0 mg/L.
5. The use of claim 4, wherein: the cut-off molecular weight of the dialysis bag is 100-.
6. Use according to one of claims 3 to 5, characterized in that: step 2) is carried out as follows: and feeding the nitrogen-doped carbon quantum dot solution and the carbon nano tube subjected to acid treatment according to the loading capacity of the nitrogen-doped carbon quantum dots, stirring for 10-60min, and drying the filtered solid particles in a vacuum oven at the temperature of 50-100 ℃ for 2-15h to obtain the carbon nano tube loaded with the carbon dots.
7. Use according to one of claims 3 to 5, characterized in that: step 3) is carried out as follows: the carbon nano tube loaded with the carbon dots obtained in the step 2) is mixed with water according to the feeding ratio of the carbon nano tube loaded with the carbon dots to the water of 1 g: 5-35ml of prepared slurry is added with corresponding aqueous solution containing metal ions according to the metal loading capacity at the temperature of 5-40 ℃ under the stirring state, the dropping speed of the aqueous solution containing metal ions is 1d/1-10s, after the dropping is finished, the stirring is continued for 2-6h, the filtration and the washing are carried out until the pH value is neutral, and the drying is carried out for 3-15h at the temperature of 50-100 ℃ to obtain the carbon nano tube embedded metal particle catalyst.
8. Use according to claim 1 or 2, characterized in that: the application method comprises the following steps:
uniformly mixing a carbon nano tube embedded metal particle catalyst with quartz sand particles, wherein the granularity of the quartz sand is 0.5-2mm, placing the mixture in a fixed bed reactor, the reaction pressure is 0.1MPa, the CO content is 1-5 mol%, and O2Content 1 mol%, H2The content is 40-80 mol%, the rest nitrogen is complemented, and the space velocity is 1000--1gcat -1The reaction temperature is 40-200 ℃.
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