DINUCLEAR RHODIUM COMPLEX-DOPED PLATINUM/HOLLOW MESOPOROUS SILICA SPHERE COMPOSITE MATERIAL, AND PREPARATION METHOD AND APPLICATION THEREOF

Abstract

The invention discloses a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material, and a preparation method and an application thereof. The preparation method comprises the following steps: preparing hollow mesoporous silica by a selective etching technology, uniformly distributed a precious metal platinum in the channels of the hollow mesoporous silica by using simple impregnation, and mixing the obtained catalyst with dinuclear rhodium complex adsorbed silica gel to obtain the composite material integrating a chromogenic probe with the catalyst. The preparation method is simple, and the chromogenic performance of the dinuclear rhodium complex material and catalysis performance of the catalyst can achieve simultaneous detection and catalyst of CO; and the dinuclear rhodium complex has obvious response to CO, and has chromogenic change in the presence of 50 ppm CO, and the product prepared through the preparation method has excellent CO detection and treatment properties, and highly facilitates industrial application.

Claims

1. A preparation method of a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material, characterized in comprising the following steps: (1) mixing ethanol, water, ammonia water and tetraethyl orthosilicate to obtain silica nanospheres; then adding tetraethyl orthosilicate and octadecyltrimethoxysilane to obtain core-shell structure silica spheres; (2) adding core-shell structure silica spheres to a sodium carbonate solution for reaction, and then calcining to obtain hollow mesoporous silica spheres; (3) after surface amination, immersing the hollow mesoporous silica spheres in a solution containing chloroplatinic acid, stirring and centrifuging, and then reduced to obtain platinum/hollow mesoporous silica spheres; (4) mixing triphenylphosphine, rhodium acetate dimer, and acetic acid under an argon atmosphere to obtain a dinuclear rhodium complex; (5) dispersing the platinum/hollow mesoporous silica spheres and dinuclear rhodium complex in ethanol containing silica gel to obtain a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material.

2. A method of detection and/or treating CO, characterized in comprising the following steps: (1) mixing ethanol, water, ammonia water and tetraethyl orthosilicate to obtain silica nanospheres; then adding tetraethyl orthosilicate and octadecyltrimethoxysilane to obtain core-shell structure silica spheres; (2) adding core-shell structure silica spheres to a sodium carbonate solution for reaction, and then calcining to obtain hollow mesoporous silica spheres; (3) after surface amination, immersing the hollow mesoporous silica spheres in a solution containing chloroplatinic acid, stirring and centrifuging, and then reduced to obtain platinum/hollow mesoporous silica spheres; (4) mixing triphenylphosphine, rhodium acetate dimer, and acetic acid under an argon atmosphere to obtain a dinuclear rhodium complex; (5) dispersing the platinum/hollow mesoporous silica spheres and dinuclear rhodium complex in ethanol containing silica gel to obtain a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material; (6) placing the platinum/hollow mesoporous silica spheres or the dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material in an environment containing CO to complete detection and/or treatment of CO.

3. A preparation method of platinum/hollow mesoporous silica spheres, characterized in comprising the following steps: (1) mixing ethanol, water, ammonia water and tetraethyl orthosilicate to obtain silica nanospheres; then adding tetraethyl orthosilicate and octadecyltrimethoxysilane to obtain core-shell structure silica spheres; (2) adding core-shell structure silica spheres to a sodium carbonate solution for reaction, and then calcining to obtain hollow mesoporous silica spheres; (3) after surface amination, immersing the hollow mesoporous silica spheres in a solution containing chloroplatinic acid, stirring and centrifuging, and then reduced to obtain platinum/hollow mesoporous silica spheres.

4. The method according to claim 1, wherein in the step (1), the mass ratio of ethanol, water, ammonia water, tetraethyl orthosilicate is (580590):(90110):(032):(5055), first, the ethanol, water and ammonia water are mixed and stirred at room temperature for 20 to 30 minutes, then tetraethyl orthosilicate is added, stirred for 5 to 10 minutes, and then allowed to stand for 60 to 90 minutes to obtain silica nanospheres; then tetraethyl silicate and octadecyltrimethoxysilane are added, and stand at room temperature for 2 to 4 hours to obtain core-shell silica spheres; in the step (2), the concentration of the sodium carbonate solution is 0.5 to 0.7 mol/L; the reaction temperature is 70 to 90 C., the time is 1 to 2 hours; during calcination, the heating rate is 2 to 10 C./min, the time is 5 to 10 h, and the temperature is 500 to 600 C.

5. The method according to claim 1, wherein in the step (3), the surface amination reagent is 3-aminopropyltriethoxysilane, the solvent is ethanol; and the surface amination temperature is 100 C.130 C., time is 2436 hours; the mass ratio of 3-aminopropyl triethoxysilane, ethanol and hollow mesoporous silica sphere is (1020):(190 210):(25); stirring treatment is carried out under vacuum for 5 to 10 hours; in the reducing process, the heating rate is 2 to 5 C./min, the time is 2 to 4 hours, the temperature is 200 to 300 C.; in the solution containing chloroplatinic acid, the solvent is water, the concentration is 20 mmol/L; when reducing, the reducing agent is hydrogen.

6. The method according to claim 1, wherein in the step (4), the mass ratio of triphenylphosphine, rhodium acetate dimer, and acetic acid is (12):(12):(100150), the temperature is 120 C.150 C., the time is 30 to 60 minutes.

7. The method according to claim 1, wherein in the step (5), the mass ratio of platinum/hollow mesoporous silica spheres, dinuclear rhodium complex, ethanol and silica gel is (12):(25):(5060):(2040).

8. A dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material prepared by the preparation method of a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material according to claim 1.

9. The application of the dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material according to claim 8 in the detection and treatment of CO.

10. (canceled)

11. The method according to claim 2, wherein in the step (1), the mass ratio of ethanol, water, ammonia water, tetraethyl orthosilicate is (580590):(90110):(032):(50 55), first, the ethanol, water and ammonia water are mixed and stirred at room temperature for 20 to 30 minutes, then tetraethyl orthosilicate is added, stirred for 5 to 10 minutes, and then allowed to stand for 60 to 90 minutes to obtain silica nanospheres; then tetraethyl silicate and octadecyltrimethoxysilane are added, and stand at room temperature for 2 to 4 hours to obtain core-shell silica spheres; in the step (2), the concentration of the sodium carbonate solution is 0.5 to 0.7 mol/L; the reaction temperature is 70 to 90 C., the time is 1 to 2 hours; during calcination, the heating rate is 2 to 10 C./min, the time is 5 to 10 h, and the temperature is 500 to 600 C.

12. The method according to claim 2, wherein in the step (3), the surface amination reagent is 3-aminopropyltriethoxysilane, the solvent is ethanol; and the surface amination temperature is 100 C.130 C., time is 2436 hours; the mass ratio of 3-aminopropyl triethoxysilane, ethanol and hollow mesoporous silica sphere is (1020):(190 210):(25); stirring treatment is carried out under vacuum for 5 to 10 hours; in the reducing process, the heating rate is 2 to 5 C./min, the time is 2 to 4 hours, the temperature is 200 to 300 C.; in the solution containing chloroplatinic acid, the solvent is water, the concentration is 20 mmol/L; when reducing, the reducing agent is hydrogen.

13. The method according to claim 2, wherein in the step (4), the mass ratio of triphenylphosphine, rhodium acetate dimer, and acetic acid is (12):(12):(100150), the temperature is 120 C.150 C., the time is 30 to 60 minutes.

14. The method according to claim 2, wherein in the step (5), the mass ratio of platinum/hollow mesoporous silica spheres, dinuclear rhodium complex, ethanol and silica gel is (12):(25):(5060):(2040).

15. The method according to claim 3, wherein in the step (1), the mass ratio of ethanol, water, ammonia water, tetraethyl orthosilicate is (580590):(90110):(032):(50 55), first, the ethanol, water and ammonia water are mixed and stirred at room temperature for 20 to 30 minutes, then tetraethyl orthosilicate is added, stirred for 5 to 10 minutes, and then allowed to stand for 60 to 90 minutes to obtain silica nanospheres; then tetraethyl silicate and octadecyltrimethoxysilane are added, and stand at room temperature for 2 to 4 hours to obtain core-shell silica spheres; in the step (2), the concentration of the sodium carbonate solution is 0.5 to 0.7 mol/L; the reaction temperature is 70 to 90 C., the time is 1 to 2 hours; during calcination, the heating rate is 2 to 10 C./min, the time is 5 to 10 h, and the temperature is 500 to 600 C.

16. The method according to claim 3, wherein in the step (3), the surface amination reagent is 3-aminopropyltriethoxysilane, the solvent is ethanol; and the surface amination temperature is 100 C.130 C., time is 2436 hours; the mass ratio of 3-aminopropyl triethoxysilane, ethanol and hollow mesoporous silica sphere is (1020):(190 210):(25); stirring treatment is carried out under vacuum for 5 to 10 hours; in the reducing process, the heating rate is 2 to 5 C./min, the time is 2 to 4 hours, the temperature is 200 to 300 C.; in the solution containing chloroplatinic acid, the solvent is water, the concentration is 20 mmol/L; when reducing, the reducing agent is hydrogen.

17. The method according to claim 3, wherein in the step (4), the mass ratio of triphenylphosphine, rhodium acetate dimer, and acetic acid is (12):(12):(100150), the temperature is 120 C.150 C., the time is 30 to 60 minutes.

18. The method according to claim 3, wherein in the step (5), the mass ratio of platinum/hollow mesoporous silica spheres, dinuclear rhodium complex, ethanol and silica gel is (12):(25):(5060):(2040).

19. Platinum/hollow mesoporous silica spheres prepared by the preparation method of platinum/hollow mesoporous silica spheres according to claim 3.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0049] FIG. 1: TEM images of the HMSs.

[0050] FIG. 2: SEM images of the HMSs.

[0051] FIG. 3: TEM images of the Pt/HMSs.

[0052] FIG. 4: SEM images of the Pt/HMSs.

[0053] FIG. 5: CO conversion as a function of reaction temperature.

[0054] FIG. 6: Durability of Pt/HMSs for CO oxidation.

[0055] FIG. 7: Photograph showing the color modulation of Pt/HMSs-BRC in contact with an air atmosphere containing 50 ppm of CO.

DETAILED DESCRIPTION OF THE INVENTION

Embodiment 1

[0056] Preparation of Hollow Mesoporous Silica (HMSs), the Specific Steps are as Follows:

[0057] 58.5 g of ethanol, 10 g of deionized water, and 3.1 g of ammonia solution are mixed and stirred for 30 min at room temperature. Then, 5.2 g of TEOs is added to the above mixture with vigorous stirring for 10 min and left stationary for 60 min. Then 3.33 g of TEOs and 1.51 g of C.sub.18TMOs are mixed and added into the above mixture and stirred for 1 min. The mixed solution is kept for 3 h without stirring at room temperature, separated by centrifugation to obtain sSiO.sub.2@mSiO.sub.2. The product is selectively etched at 80 C. for 2 h with a sodium carbonate solution having a concentration of 0.6 mol/L. After drying, it is calcined in air atmosphere with the heating rate of 5 C./min to 550 C. for 6 h to get HMSs.

[0058] FIG. 1 shows the TEM images of the HMSs. FIG. 2 shows the SEM images of the HMSs. The figures show the uniform hollow sphere structure, and the distribution is more uniform.

Embodiment 2

[0059] Preparation of Platinum/Hollow Mesoporous Silica Composites (Pt/HMSs), the Specific Steps are as Follows:

[0060] The HMSs are first subjected to surface amination modification, 2 g of HMSs are added to 200 ml of ethanol containing 10 g of 3-aminopropyltriethoxysilane, followed by heating under reflux for 24 hours, centrifugation, and washing with ethanol and water. The resulting aminated silica is then added to different concentrations of chloroplatinic acid in aqueous solutions at concentrations of 5 mmol/L, 10 mmol/L, and 20 mmol/L (corresponding to Pt/HMSs loadings of 1%, 3%, 5% platinum), then stirred under vacuum for 3 h, centrifuged, and calcined under a hydrogen atmosphere at a heating rate of 2.5 C./min for 3 h at a temperature of 300 C.

[0061] FIG. 3 is a TEM image of Pt/HMSs, and FIG. 4 is an SEM image of Pt/HMSs. It can be seen from the TEM image that the platinum nanoparticles are successfully loaded into the pores of the HMSs and the distribution is relatively uniform. It can be seen from the SEM image that the silica sphere after loading did not change significantly, which was consistent with the morphology before loading.

[0062] The prepared 50 mg of Pt/HMSs is placed in a 1% CO environment for catalytic CO oxidation. The specific CO conversion effect is analyzed by gas chromatography. That is, a standard curve is established by the standard gas, and the concentration of CO is recorded as 1, and then as the catalysis progresses, the concentration gradually decreases, thereby obtaining a specific CO conversion result. FIG. 5 is a graph showing the conversion of CO by Pt/HMSs, and FIG. 6 is a stability test of the catalyst. As can be seen from FIG. 5, the catalyst loaded with 5% platinum is optimal in the same time, and a catalytic effect of 100% can be achieved at 170 C. If the loading of platinum is too much, it will easily lead to metal agglomeration, which will lead to a decrease in catalytic effect. The effect of 6% platinum is worse than 5%. FIG. 6 shows the stability test of Pt/HMSs (loaded with 5% platinum). Within a few hours, its catalytic activity is not substantially reduced, which is beneficial to the practical application of the present invention. The atmospheric CO pollution mainly comes from the emission of automobile exhaust gas, and the calculation method of CO conversion rate is as follows:

[00001]$\begin{array}{cc}=\frac{C_0-C}{C_0}100.Math.\%& \left(1\right)\end{array}$

[0063] C.sub.0 and C are the initial and test concentrations of CO in the experiment (tested every 30 minutes).

Embodiment 3

[0064] Preparation of a Dinuclear Rhodium Complex:

[0065] 0.15 g of triphenylphosphine and 0.15 g of rhodium acetate dimer are added to 10 to 20 ml of acetic acid at a heating temperature of 120 to 150 C. for a reflux time of 45 minutes, and then a purple product dinuclear rhodium complex is obtained.

Embodiment 4

[0066] Preparation of Dinuclear Rhodium Complex-Doped Platinum/Hollow Mesoporous Silica Sphere Composite Material, Detection and Catalytic Oxidation of CO:

[0067] 100 mg of Pt/HMSs and 200 mg of the detector dinuclear rhodium complex are separately dispersed in 5 ml of ethanol, and adsorbed in 2 g of silica gel to prepare a dinuclear rhodium complex-doped platinum/hollow mesoporous silica sphere composite material. Due to the porosity of silica gel, the detection agent and the catalyst can have a better adsorption effect, facilitate the thorough mixing of the two, and demonstrate good synergy. The obtained composite material is placed in a 50 ppm CO environment, and its color change is observed. The specific process is shown in FIG. 7, in which (a) shows the color after mixing. It can be seen as purple from the figure. With the introduction of CO gas, it can be seen that the color turns orange after 70 s, indicating that the detector is combined with CO. As the temperature increases, the catalyst began to be activated, and the color turned pale yellow at 40 minutes, and as the catalyst is continuously catalyzed, the color completely returned to purple after 60 minutes.

[0068] In the CO catalyst disclosed by the invention, hollow mesoporous silica is selected as a carrier, and the noble metal platinum is uniformly loaded into the pores thereof, and the platinum nanoparticles have high catalytic activity, especially after loading the hollow mesoporous silica, the catalytic activity is greatly improved; the silica material has the advantages of high specific surface area, good stability, controllable structure, high porosity, etc.; as the dinuclear rhodium complex of the invention is highly selective and sensitive to CO, it has a good advantage in the detection of CO. The invention combines the detection material with the catalyst to make it more widely used in the treatment of CO waste gas.