Synthesis strategy of supported transition metal carbides Fenton-like catalysts and application thereof

Abstract

The invention is mainly related to a synthesis method of supported two-dimensional transition metal carbides for Fenton-like catalysis, which includes the following steps: (1) preparing two-dimensional transition metal carbides powders; (2) dispersing the two-dimensional transition metal carbides powders into intercalants solution to perform an intercalation reaction, and then centrifuging, washing, and freeze-drying to obtain intercalated products; (3) dispersing a certain quality previously obtained intercalated powders into ultrapure water and heating for pre-reaction, and then adding hydrogen peroxide solution to the pre-reacted mixed solution under ice-water bath for secondary etching, resting, centrifuging and gently decanting a supernatant to obtain the final Fenton-like catalysts.

Claims

1. A synthesis method of supported two-dimensional transition metal, Fenton catalysts, the method comprising as follows: (1) preparing two-dimensional transition metal carbide powders; (2) dispersing the two-dimensional transition metal carbide powders into intercalants solution to perform an intercalation reaction, and then centrifuging, washing, and freeze-drying to obtain intercalated products; (3) dispersing a certain quality previously obtained intercalated products into ultrapure water and heating for a pre-reacted mixed solution, and then adding hydrogen peroxide solution to the pre-reacted mixed solution under ice-water bath for secondary etching, resting, centrifuging and gently decanting a supernatant to obtain the final Fenton catalysts.

2. The method of claim 1, wherein the transition metal in the catalyst is a variable valence transition metal element, selected from one or more of Ti, V, Nb, Mo, or Ta.

3. The method of claim 1, wherein in step (1), a method for preparing the two-dimensional transition metal carbide powders comprises: adding a ternary layered MAX phase ceramic material to hydrofluoric acid (HF) at room temperature along with magnetic stirring to remove the Al layer, wherein nitrogen (N.sub.2) is passed into a system, aiming to exhaust oxygen and prevent oxidation; centrifuging a suspension; washing with ethanol and deionized water; and freeze-drying to obtain the two-dimensional transition metal carbide powders.

4. The method of claim 3, wherein in step (1), a mass-volume ratio of the ternary layered MAX phase ceramic material and the hydrofluoric acid solution is 1-10 g:18-100 mL; a mass concentration of the hydrofluoric acid solution is 10%-49%; the etching reaction is at room temperature along with magnetic stirring for 12-120 h; and the obtained two-dimensional transition metal carbide powders are freeze-dried under the condition of −30° C.-50° C. for 48-60 h.

5. The method of claim 1, wherein in step (2), a mass-volume ratio of the two-dimensional transition metal carbide powders and the intercalants solution is 0.5-10 g:20-50 mL; the intercalants solution is tetrapropylammonium hydroxide solution; a mass concentration of the tetrapropylammonium hydroxide solution is 20%-50%; the intercalation reaction is at room temperature along with magnetic stirring for 12-72 h; and the obtained intercalated products are freeze-dried under the condition of −30° C.-50° C. for 48-60 h.

6. The method of claim 1, wherein in step (3), a mass-volume ratio of the intercalated products and the ultrapure water is 0.05-0.5 g:10-50 mL; a mass-volume ratio of the intercalated products and the hydrogen peroxide solution is 0.05-0.5 g:0.5-5 mL; and a mass concentration of the hydrogen peroxide solution is 10%-50%.

7. The method of claim 1, wherein in step (3), the pre-reacted mixed solution is heated in an oil bath along with magnetic stirring for 10-30 min, and a reaction temperature is 30-50° C.

8. The method of claim 1, wherein in step (3), a resting time is 30-60 min.

9. The method of claim 1, wherein a speed of the centrifugation is 8000-12000 rpm, and a centrifugation time is 10-30 min.

10. A supported two-dimensional transition metal carbide Fenton catalyst obtained by the method of claim 1, wherein the catalyst is used for a catalytic degradation of organic pollutants in water or soil mediums under dark conditions.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is X-ray diffraction patterns of supported titanium-based Fenton-like catalyst.

(2) FIG. 2 is a digital photo of supported titanium-based Fenton-like catalyst.

(3) FIG. 3 is a representative TEM image of supported titanium-based Fenton-like catalyst.

(4) FIG. 4 is a Fenton-like catalytic performance of supported titanium-based Fenton-like catalyst towards atrazine under dark.

DESCRIPTION OF THE EMBODIMENTS

(5) The invention will be described in detail in combination with specific examples. The following examples will help researchers to further understand this invention and not be limited to the example embodiments set forth herein. However, this disclosure may be embodied easily by those who have common knowledge in the related art, these all belong to the protection scope of the present invention.

(6) An in-situ oxidation synthesis method of Fenton-like catalysts, which is mainly related to supported two-dimensional transition metal carbides, comprising as follows: (1) A synthesis and delamination of multilayer two-dimensional transition metal carbides were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1-10 g ternary layered MAX phase ceramic materials were added to 18-100 mL of 10-49 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into a system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12-120 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained two-dimensional transition metal carbides powders were freeze-dried under the condition of −30° C.-50° C. for 48-60 h and stored at 4° C. (2) The two-dimensional transition metal carbides powders were dispersed into tetrapropylammonium hydroxide (TPAOH) intercalants solution to perform an intercalation reaction. Briefly, 0.5-10 g of the previously obtained two-dimensional transition metal carbides powder was stir-mixed with 20-50 mL of 20-50 wt % TPAOH for 12-72 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried under the condition of −30° C.-50° C. for 48-60 h to obtain intercalated products. (3) In the process, 0.05-0.5 g previously obtained intercalated powder was dispersed in 10-50 mL deionized water by magnetic stirring near room temperature (30-50° C.) for 10-30 min. Then 0.5-5 mL, 10-30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30-60 min, the resulting dispersion was centrifuged for 10-30 min at 8000-12000 rpm, and a supernatant of the final products was gently decanted to obtain the Fenton-like catalysts.

(7) Among them, the transition metal in the catalyst is a variable valence transition metal element, preferably one or more of Ti, V, Nb, Mo, or Ta.

(8) During the preparation process, the ternary layered MAX phase ceramic materials corresponding to different two-dimensional transition metal carbides are as follows:

(9) The corresponding raw material for Ti.sub.3C.sub.2 is Ti.sub.3AlC.sub.2, V.sub.2C is V.sub.2AlC, Nb.sub.2C is Nb.sub.2AlC, Ta.sub.2C is Ta.sub.2AlC, and Mo.sub.3C.sub.2 is Mo.sub.3AlC.sub.2, respectively.

(10) The invention provides a synthesis method for supported two-dimensional transition metal carbides Fenton-like catalysts, which has potential application value in catalytic degradation of organic pollutants in water or soil mediums under dark conditions.

(11) Herein, the catalyst prepared by the method of the invention is a liquid catalyst that is through a novel, general, and facile fabrication route for direct super-growth of high-uniformity ultra-small clusters (˜2 nm) and nanodots (˜5 nm) active sites in situ within a fragmented silk-like amorphous carbon framework, whose the thickness is about 1 nm. Meanwhile, the MO.sub.x active sites express the features of high-dispersity and high-uniformity and high degree of defect for Fenton-like catalysis.

(12) This invention has more advantages of high reactivity, low cost, well stability and reusability, wide pH range, and easy conversion compared with other techniques, which has potential application value in water quality, air purification, soil remediation and new energy resources fields.

(13) Hereinafter, the present inventive concepts will be described in more details with reference to the following Examples and attached Figures.

Example 1

(14) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into a system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 12 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

(15) As shown in FIG. 1, X-ray diffraction didn't show any signal about Anatase or Rutile, which further confirmed a highly disordered structure inside or primarily because of the insensitivity to small catalytic sites.

(16) As shown in FIG. 2, the prepared catalyst could be well dispersed in water with typical Tyndall effect for several months, which indicated their excellent hydrophilicity and dispersity. As can be seen from FIG. 3, atomically dispersed high-uniformity ultra-small TiO.sub.1.47 clusters (˜2 nm) and nanodots (˜5 nm) active sites in situ anchored on fragmented silk-like amorphous carbon framework (AD-TiO.sub.1.47/A-carbon).

(17) ATZ was chosen to screen the optimized catalyst and assess the catalytic performance of the as-prepared sample for Fenton-like activation. In a typical degradation process, a determined amount of powder catalyst was mixed into 20 mL, 5 mg.Math.L.sup.−1ATZ solution. The mass of comparison samples was determined according to the concentration of the titanium element of AD-TiO.sub.1.47/A-carbon, which we confirmed all these Ti species could contribute to the Fenton-like reaction. In this system, the final concentration of Ti element was 100 mg.Math.L.sup.−1. Thereafter, the 5 mM of H.sub.2O.sub.2 was introduced into the solution to initialize the reaction. At pre-specified time intervals (0, 10, 20, 30, 40 and 50 min), 2 mL reaction solution was withdrawn from each tube and quenched by 2 mL 1.5 mM Na.sub.2SO.sub.3 solutions immediately (1:1). Afterwards, the solutions were filtered with 0.22 μm membrane to remove impurity solids and send for high performance liquid chromatography (HPLC) analysis to measure ATZ concentration. Specially, the AD-TiO.sub.1.47/A-carbon should be separated from the catalyst-pollutant solution using Waters Oasis HLB SPE columns (3 cc/60 mg, 30 um). All catalytic experiments were at least carried out in duplicates with standard errors reported. As shown in FIG. 4, as high as 95% ATZ removal could be achieved in 30 min using AD-TiO.sub.1.47/A-carbon as the catalyst, yet the rest of as-prepared samples and H.sub.2O.sub.2 alone hardly degrade the pollutants.

Example 2

(18) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into a system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 72 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 3

(19) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into a system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 120 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 10.00 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 50 mL TPAOH for 72 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 4

(20) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 5.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 90 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 5

(21) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 10.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 100 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 6

(22) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.05 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 7

(23) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 8

(24) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.50 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 50 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 9

(25) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 10% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 10

(26) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 50% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 11

(27) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 60 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 12

(28) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 0.5 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 13

(29) A novel preparation method of supported titanium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ti.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ti.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 48 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ti.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ti.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ti.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 48 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ti.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Ti.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 5 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported titanium-based Fenton-like catalyst.

Example 14

(30) A novel preparation method of supported vanadium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer V.sub.2C were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase V.sub.2AlC powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained V.sub.2C powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of V.sub.2C was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained V.sub.2C dry powder was stir-mixed with 20 mL TPAOH for 12 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain V.sub.2C MXene powder. (3) In the process, 0.10 g previously obtained V.sub.2C MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported vanadium-based Fenton-like catalyst.

(31) Fenton-like catalytic performance was evaluated for ATZ removal via activation of H.sub.2O.sub.2. The steps of the degradation reaction were the same as those in Example 1. As the degradation efficiency test, as high as 95% ATZ removal could be achieved in 30 min using 100 ppm supported niobium-based Fenton-like catalyst under the dark conditions.

Example 15

(32) A novel preparation method of supported niobium-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Nb.sub.2C were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Nb.sub.2AlC powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12 h to remove the Al layer (Rotation speed is 300 rpm). The suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Nb.sub.2C powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Nb.sub.2C was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Nb.sub.2C dry powder was stir-mixed with 20 mL TPAOH for 12 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Nb.sub.2C MXene powder. (3) In the process, 0.10 g previously obtained Nb.sub.2C MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported niobium-based Fenton-like catalyst.

(33) Fenton-like catalytic performance was evaluated for ATZ removal via activation of H.sub.2O.sub.2. The steps of the degradation reaction were the same as those in Example 1. As the degradation efficiency test, as high as 95% ATZ removal could be achieved in 30 min using 100 ppm supported niobium-based Fenton-like catalyst under the dark conditions.

Example 16

(34) A novel preparation method of supported tantalum-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Ta.sub.2C were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Ta.sub.2AlC powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Ta.sub.2C powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Ta.sub.2C was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Ta.sub.2C dry powder was stir-mixed with 20 mL TPAOH for 12 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Ta.sub.2C MXene powder. (3) In the process, 0.10 g previously obtained Ta.sub.2C MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported tantalum-based Fenton-like catalyst.

(35) Fenton-like catalytic performance was evaluated for ATZ removal via activation of H.sub.2O.sub.2. The steps of the degradation reaction were the same as those in Example 1. As the degradation efficiency test, as high as 95% ATZ removal could be achieved in 30 min using 100 ppm supported tantalum-based Fenton-like catalyst under the dark conditions.

Example 17

(36) A novel preparation method of supported molybdenum-based Fenton-like catalyst for highly reactive and stable catalytic degradation of a series of organic pollutants under the dark filed through the advanced oxidation technology. The method comprising as follows: (1) A synthesis and delamination of multilayer Mo.sub.3C.sub.2 were achieved by a liquid exfoliation method using hydrofluoric acid (HF) etching. Briefly, 1.00 g MAX phase Mo.sub.3AlC.sub.2 powder was added to 18 mL of 40 wt % hydrofluoric acid (HF), which passed nitrogen (N.sub.2) into the system for 30 min, aiming to exhaust oxygen and prevent oxidation, at room temperature along with magnetic stirring for 12 h to remove the Al layer (Rotation speed is 300 rpm). A suspension was then centrifuged, followed by washing with ethanol and deionized water until pH>6. Finally, the obtained Mo.sub.3C.sub.2 powder was freeze-dried for 48 h and stored at 4° C. (2) Then, the delamination of Mo.sub.3C.sub.2 was conducted using tetrapropylammonium hydroxide (TPAOH) after HF etching. Briefly, 0.50 g of the previously obtained Mo.sub.3C.sub.2 dry powder was stir-mixed with 20 mL TPAOH for 12 h at room temperature, followed by collecting after centrifugation (Rotation speed is 300 rpm) with washing by ethanol and deionized water for three times until pH>6. A final aqueous dispersion was freeze-dried to obtain Mo.sub.3C.sub.2 MXene powder. (3) In the process, 0.10 g previously obtained Mo.sub.3C.sub.2 MXene dry powder was dispersed in 10 mL deionized water by magnetic stirring near room temperature (30° C.) for 10 min. Then 1 mL, 30% H.sub.2O.sub.2 was added, kept below 277 K under ice-water bath for 30 min, the resulting dispersion was centrifuged for 20 min at 8000 rpm, and a supernatant of the final products was gently decanted to obtain the supported molybdenum-based Fenton-like catalyst.

(37) Fenton-like catalytic performance was evaluated for ATZ removal via activation of H.sub.2O.sub.2. The steps of the degradation reaction were the same as those in Example 1. As the degradation efficiency test, as high as 95% ATZ removal could be achieved in 30 min using 100 ppm supported molybdenum-based Fenton-like catalyst under the dark conditions.

(38) While example embodiments have been described with reference to the figures, it is to be understood that the present invention is not limited to the embodiments described above, encompasses any embodiments within the scope of the following claims.