Photothermal Catalytic Method for Production of Hydrogen Peroxide without Sacrificial Reagents on Basis of Porphyrin-based Supermolecule

Abstract

A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of a porphyrin-based supermolecule is provided. The method includes the following steps: uniformly mixing a porphyrin-based supermolecule photocatalyst with a concentration of 0.3-1.5 g/L with ultrapure water, conducting irradiation with a visible light for a period of time under stirring at a temperature of 40-80° C. and an O.sub.2 flow rate of 50-150 mL/min, and then filtering and concentrating a reaction liquid to obtain an aqueous hydrogen peroxide solution with a high concentration. According to the new photothermal catalytic method for preparing the hydrogen peroxide provided in the present disclosure, no organic solvent (such as ethanol, isopropanol and benzyl alcohol) is used as a sacrificial reagent, and the method is environmentally friendly and free of pollution. O.sub.2 is used as an oxygen source, sunlight is used as an energy source, and the method is low in energy consumption and high in safety (compared with an industrial anthraquinone method for synthesizing hydrogen peroxide). The method is simple in operation, mild in reaction conditions and high in production of the hydrogen peroxide.

Claims

1. A method for photothermal catalytic production of hydrogen peroxide without a sacrificial reagent on the basis of a porphyrin-based supermolecule, comprising the following steps: (1) ultrasonically dispersing a porphyrin catalyst in water to obtain a porphyrin catalyst dispersion with a concentration of 0.3-1.5 g/L of the porphyrin catalyst, wherein the porphyrin catalyst is at least one selected from the group consisting of 5,10,15,20-tetrakis(4-methoxycarbonylphenyl)porphyrin (TPP-COOMe), 5,10,15,20-tetrakis(4-sulfophenyl)porphyrin (TPPS), 5,10,15,20-tetrakis(4-hydroxyphenyl)porphyrin (THPP), 5,10,15,20-tetrakis(4-aminophenyl)porphyrin (TAPP), 5,10,15,20-tetrakis(4-pyridyl)porphyrin (TPyP), and 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin (TCPP); (2) continuously introducing O.sub.2 into the porphyrin catalyst dispersion obtained in step (1) at a temperature of 40-80° C., and conducting stirring and irradiation with a visible light for a reaction for a period of time; and (3) filtering a reaction product obtained in step (2) to obtain an aqueous hydrogen peroxide solution.

2. The method according to claim 1, wherein the porphyrin catalyst is at least one selected from the group consisting of 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin, 5,10,15,20-tetrakis(4-hydroxyphenyl)porphyrin and 5,10,15,20-tetrakis(4-sulfophenyl)porphyrin.

3. The method according to claim 2, wherein the porphyrin catalyst is 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin.

4. The method according to claim 1, wherein, in step (2), the reaction is carried out at a temperature of 60° C.

5. The method according to claim 1, wherein, in step (2), the oxygen is introduced at a flow rate of 50-150 mL/min.

6. The method according to claim 5, wherein, in step (2), the oxygen is introduced at a flow rate of 80 mL/min.

7. The method according to claim 1, wherein, in step (3), the visible light has a light intensity of 80-150 mW/cm.sup.2.

8. The method according to claim 7, wherein, in step (3), the visible light has a light intensity of 90 mW/cm.sup.2.

9. The method according to claim 1, wherein, in step (2), the irradiation is conducted for 2-24 hours.

10. The method according to claim 1, wherein, an amount ratio of the porphyrin catalyst to the water is 1 mg: 2 mL.

11. The method according to claim 1, wherein, in step (2), the visible light is provided by a xenon lamp with an additional 420 nm cut-off filter.

12. The method according to claim 1, wherein, after the filtering is completed, the step (3) further comprises concentrating a filtrate.

13. The method according to claim 1, wherein the step (3) further comprises washing a filter cake with ultrapure water, drying the washed filter cake and recovering the porphyrin catalyst.

Description

BRIEF DESCRIPTION OF FIGURES

[0041] FIG. 1 is a diagram showing the production performance of hydrogen peroxide by photothermal catalysis with different porphyrins (in Examples 1 to 6);

[0042] FIG. 2 is a transmission electron microscopy (TEM) image of a TCPP catalyst in Example 8;

[0043] FIG. 3 is an atomic force microscopy (AFM) image of the TCPP catalyst in Example 8;

[0044] FIG. 4 is a diagram showing a relationship between the concentration of hydrogen peroxide produced by photothermal catalysis with the TCPP and the reaction temperature (in Example 6, Examples 13 to 14 and Comparative Example 1); and

[0045] FIG. 5 is a diagram showing a relationship between the concentration of hydrogen peroxide produced by photothermal catalysis with the TCPP and the reaction time (in Example 6 and Examples 15 to 19).

DETAILED DESCRIPTION

[0046] The present disclosure will be further described below in conjunction with specific examples, but the protection scope of the present disclosure is not limited thereto.

Method for Determining the Concentration of Hydrogen Peroxide

[0047] Hydrogen peroxide and potassium titanium oxalate may form a yellow complex solution. The absorbance of the complex solution at 400 nm is measured by using an ultraviolet spectrophotometer. The concentration of the hydrogen peroxide is calculated by using a Lambert-Beer law. The method specifically includes the following steps. 1 mL of a sample to be ed (a reaction liquid in examples or comparative examples) is taken every 1 h and filtered with a 0.45 μm filter membrane to remove catalyst particles. Then, 1 mL of a potassium titanium oxalate solution (0.02 M) and 3 mL of ultrapure water are added to obtain a mixed solution. At last, the concentration of the H.sub.2O.sub.2was calculated based on the absorbance at 400 nm monitored by a UV-Vis spectrophotometer.

[0048] Sources of porphyrin catalysts in the present disclosure are as follows.

[0049] TPP-COOMe is purchased from Beijing Innochem Science & Technology Co., Ltd., and has a purity of 97%.

[0050] TPPS is purchased from Sigma-Aldrich Biochemical Technology Co., Ltd., and has a purity of 85%.

[0051] THPP is purchased from Beijing Innochem Science & Technology Co., Ltd., and has a purity of 97%.

[0052] TAPP is purchased from Aladdin Chemical Reagent Co., Ltd., and has a purity of 95%.

[0053] TPyP is purchased from Shanghai Haohong Biomedical Technology Co., Ltd., and has a purity of 97%.

[0054] TCPP is purchased from Beijing Innochem Science & Technology Co., Ltd., and has a purity of 97%.

EXAMPLE 1

[0055] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TPP-COOMe included the following steps.

[0056] 25 mg of the TPP-COOMe catalyst was dispersed evenly by ultrasound in 50 mL of ultrapure water in a 100 mL flask. Heating (at 60° C.) and magnetic stirring were conducted in an oil bath pot, O.sub.2 flow rate was 80 mL/min, and irradiation was conducted by using a xenon lamp (π≥420 nm) with a light intensity of 90 mW/cm.sup.2 for 4 h.

[0057] 1 mL of a reaction liquid was taken every 1 h and filtered with a 0.45 μm filter membrane to remove the catalyst. Then, 1 mL of a potassium titanium oxalate solution (0.02 M) and 3 mL of ultrapure water were added to obtain a mixed solution. The absorbance of the mixed solution at 400 nm was measured by using an ultraviolet spectrophotometer, and the concentration of the hydrogen peroxide was calculated by using a Lambert-Beer law.

EXAMPLE 2

[0058] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TPPS was provided. With Example 1 as a reference, the only difference was that the type of the porphyrin catalyst was changed, and specifically, the TPP-COOMe was changed to the TPPS.

EXAMPLE 3

[0059] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of THPP was provided. With Example 1 as a reference, the only difference was that the type of the porphyrin catalyst was changed, and specifically, the TPP-COOMe was changed to the THPP.

EXAMPLE 4

[0060] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TAPP was provided. With Example 1 as a reference, the only difference was that the type of the porphyrin catalyst was changed, and specifically, the TPP-COOMe was changed to the TAPP.

EXAMPLE 5

[0061] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TPyP was provided. With Example 1 as a reference, the only difference was that the type of the porphyrin catalyst was changed, and specifically, the TPP-COOMe was changed to the TPyP.

EXAMPLE 6

[0062] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 1 as a reference, the only difference was that the type of the porphyrin catalyst was changed, and specifically, the TPP-COOMe was changed to the TCPP. The method specifically included the following steps.

[0063] 25 mg of the TCPP catalyst was dispersed evenly by ultrasound in 50 mL of ultrapure water in a 100 mL borosilicate flask sealed by a rubber cap with a pinhole. Heating (at 60° C.) and magnetic stirring were conducted in an oil bath pot, O.sub.2 flow rate was 80 mL/min, and irradiation was conducted by using a xenon lamp (λ≥420 nm) for 4 h.

[0064] 1 mL of a reaction liquid was taken every 1 h and filtered with a 0.45 μm filter membrane to remove the catalyst. Then, 1 mL of a potassium titanium oxalate solution (0.02 M) and 3 mL of ultrapure water were added to obtain a mixed solution. The absorbance of the mixed solution at 400 nm was measured by using an ultraviolet spectrophotometer, and the concentration of the hydrogen peroxide was calculated by using a Lambert-Beer law.

1. Comparison of Photothermal Catalytic Performance of Different Porphyrin Catalysts (in Examples 1 to 6) in Production of Hydrogen Peroxide

[0065] FIG. 1 is a diagram showing comparison of photothermal catalytic performance of different porphyrin catalysts in Examples 1 to 6 in production of hydrogen peroxide. The irradiation is conducted for 4 h. From FIG. 1, it can be seen that when a cumulative production of the hydrogen peroxide obtained after a photothermal reaction at 60° C. for 4 h is used as an index to evaluate the photothermal catalytic ability of several porphyrin catalysts in production of the hydrogen peroxide, the photothermal catalytic ability of the several porphyrin catalysts in production of the hydrogen peroxide is in descending order as follows: TCPP>THPP>TPPS>TPyP>TPP-COOMe>TAPP. Specifically, the TCPP has the highest catalytic activity, and the hydrogen peroxide produced has a concentration of 123 mM/g (that is, 0.37 wt %). The THPP has the second highest catalytic activity, and the hydrogen peroxide produced has a concentration of 103 mM/g. The hydrogen peroxide produced by using the TPPS, the TPyP, the TPP-COOMe and the TAPP has a concentration of 95 mM/g, 87 mM/g, 80 mM/g and 72 mM/g respectively.

2. Morphology Characterization of the TCPP Photothermal Catalyst in Example 6

[0066] Morphology characterization was conducted on the TCPP photothermal catalyst with the best photothermal catalytic performance in production of hydrogen peroxide. FIG. 2 is a TEM image of the TCPP photothermal catalyst. The TEM image shows the morphology of the TCPP, the TCPP is a sheet with a size of about 4 μm×5 μm, and due to this large-sized sheet structure, more active sites are provided for the TCPP in production of the hydrogen peroxide. FIG. 3 is an AFM image of the TCPP. The AFM image shows that the TCPP has a nanosheet structure with a thickness of about 9.5 nm. Due to the nanometer thickness, rapid transfer of photogenerated carriers from the interior of the catalyst to the surface is facilitated, that is to say, separation and transfer rates of photogenerated electron-hole pairs are increased, and therefore, the photothermal catalytic efficiency is improved. Therefore, compared with other porphyrin catalysts, the TCPP has higher catalytic activity likely due to this large and thin nanosheet morphology structure.

EXAMPLE 7

[0067] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the amount of the TCPP catalyst was changed from 25 mg to 15 mg.

EXAMPLE 8

[0068] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the amount of the TCPP catalyst was changed from 25 mg to 50 mg.

3. Influence of the Amount of the TCPP Photothermal Catalyst (in Examples 6 to 8) on Photothermal Performance in Production of Hydrogen Peroxide

[0069] The influence of the amount of the TCPP photothermal catalyst (in Examples 6 to 8) on photothermal performance in production of hydrogen peroxide is shown in Table 1.

TABLE-US-00001 TABLE 1 Influence of the amount of the TCPP photothermal catalyst (in Examples 6 to 8) on photothermal performance in production of hydrogen peroxide Amount Amount Oxygen Concentration of TCPP of water Temperature flow rate Irradiation of hydrogen Example (mg) (mL) (° C.) (mL/min) time (h) peroxide 6 25 50 60 80 4 123 mM/g (that is, 0.37 wt %) 7 15 50 60 80 4 42 mM/g (that is, 0.13 wt %) 8 50 50 60 80 4 70 mM/g (that is, 0.21 wt %)

[0070] From comparison of the data in Table 1, it can be seen that when the ultrapure water is 50 mL, the temperature is 60° C., the oxygen flow rate is 80 mL/min and the irradiation time is 4 h, by optimizing the production of the hydrogen peroxide produced by photothermal catalysis with the TCPP in an amount range of 15-50 mg, the optimal amount of the TCPP is 25 mg.

EXAMPLE 9

[0071] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the amount of the ultrapure water was changed from 50 mL to 100 mL, and accordingly, a 150 mL borosilicate flask was used as a reaction vessel.

EXAMPLE 10

[0072] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the amount of the ultrapure water was changed from 50 mL to 20 mL, and accordingly, a 50 mL borosilicate flask was used as a reaction vessel.

4. Influence of the Amount of the Ultrapure Water (in Example 6 and Examples 9 to 10) on Photothermal Catalytic Performance of the TCPP Catalyst in Production of Hydrogen Peroxide

[0073]

TABLE-US-00002 TABLE 2 Influence of the amount of the ultrapure water (in Example 6 and Examples 9 to 10) on photothermal catalytic performance of the TCPP catalyst in production of hydrogen peroxide Amount Amount Oxygen Concentration of TCPP of water Temperature flow rate Irradiation of hydrogen Example (mg) (mL) (° C.) (mL/min) time (h) peroxide 6 25 50 60 80 4 123 mM/g (that is, 0.37 wt %) 9 25 100 60 80 4 39 mM/g (that is, 0.12 wt %) 10 25 20 60 80 4 66 mM/g (that is, 0.20 wt %)

[0074] From comparison of the data in Table 2, it can be seen that the amount of the ultrapure water is preferably 50 mL.

EXAMPLE 11

[0075] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the oxygen flow rate was changed from 80 mL/min to 50 mL/min.

EXAMPLE 12

[0076] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the oxygen flow rate was changed from 80 mL/min to 150 mL/min.

5. Influence of the Oxygen Flow Rate (in Example 6 and Examples 11 to 12) on Photothermal Catalytic Performance of the TCPP Catalyst in Production of Hydrogen Peroxide

[0077]

TABLE-US-00003 TABLE 3 Influence of the oxygen flow rate (in Example 6 and Examples 11 to 12) on photothermal catalytic performance of the TCPP catalyst in production of hydrogen peroxide Amount Amount Oxygen Concentration of TCPP of water Temperature flow rate Irradiation of hydrogen Example (mg) (mL) (° C.) (mL/min) time (h) peroxide 6 25 50 60 80 4 123 mM/g (that is, 0.37 wt %) 11 25 50 60 50 4 56 mM/g (that is, 0.17 wt %) 12 25 50 60 150 4 69 mM/g (that is, 0.21 wt %)

[0078] From comparison of the data in Table 3, it can be seen that the oxygen flow rate is preferably 80 mL/min. According to the research in the present disclosure, it is found that when the oxygen flow rate is high (such as 150 mL/min), increase of the yield of the hydrogen peroxide is not facilitated.

Comparative Example 1

[0079] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the reaction temperature was changed from 60° C. to 20° C. (under room temperature conditions).

EXAMPLE 13

[0080] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the reaction temperature was changed from 60° C. to 40° C.

EXAMPLE 14

[0081] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the reaction temperature was changed from 60° C. to 80° C.

6. Influence of the Reaction Temperature (in Example 6, Examples 13 to 14 and Comparative Example 1) on Photothermal Catalytic Performance of the TCPP Catalyst in Production of Hydrogen Peroxide

[0082] FIG. 4 is a diagram showing a relationship between the concentration of hydrogen peroxide produced by photothermal catalysis with the TCPP and the reaction temperature (in Example 6, Examples 13 to 14 and Comparative Example 1). From FIG. 4, it can be seen that with increase of the temperature, the catalytic activity of the TCPP is first improved and then reduced. Specifically, when the reaction temperature is increased from 20° C. to 60° C., the concentration of the hydrogen peroxide produced by a photothermal reaction is increased from 24 mM/g to 123 mM/g. When the reaction temperature is increased from 60° C. to 80° C., the concentration of the hydrogen peroxide is decreased from 123 mM/g to 69 mM/g.

[0083] Compared with the photothermal catalytic performance of the TCPP catalyst in production of hydrogen peroxide at room temperature in Comparative Example 1, when the temperature is appropriately increased during photocatalysis, the yield of the hydrogen peroxide is greatly increased. It is indicated that the TCPP catalyst has excellent photothermal catalytic performance in the production of hydrogen peroxide (in the prior art, it has not been reported that a porphyrin-based supermolecule catalyst has photothermal catalytic performance in production of hydrogen peroxide).

EXAMPLE 15

[0084] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the irradiation time was changed from 4 h to 2 h.

EXAMPLE 16

[0085] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the irradiation time was changed from 4 h to 6 h.

EXAMPLE 17

[0086] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the irradiation time was changed from 4 h to 12 h.

EXAMPLE 18

[0087] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the irradiation time was changed from 4 h to 18 h.

EXAMPLE 19

[0088] A photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP was provided. With Example 6 as a reference, the only difference was that the irradiation time was changed from 4 h to 24 h.

7. Influence of the Irradiation Time (in Example 6 and Examples 15 to 19) on Photothermal Catalytic Performance of the TCPP Catalyst in the Production of Hydrogen Peroxide

[0089] FIG. 5 is a diagram showing a relationship between the concentration of hydrogen peroxide produced by photothermal catalysis with the TCPP and the reaction time (in Example 6 and Examples 15 to 19). From FIG. 5, it can be seen that after a photothermal reaction is carried out at 60° C. for 2 h, 4 h, 6 h, 12 h, 18 h and 24 h, an aqueous hydrogen peroxide solution (hydrogen peroxide solution) with a concentration of 65 mM/g (that is, 0.19 wt %), 123 mM/g (that is, 0.37 wt %), 187 mM/g (that is, 0.56 wt %), 323 mM/g (that is, 0.97 wt %), 452 mM/g (that is, 1.36 wt %) and 570 mM/g (that is, 1.71 wt %) may be prepared respectively. After the change of slope in FIG. 5 is analyzed, it can be found that when the irradiation time is longer than 6 h, the yield of the hydrogen peroxide per unit time is slightly reduced. However, when the irradiation time lasts from 6 h to 24 h, the slope is not significantly changed, indicating that by using the photothermal catalytic method for production of hydrogen peroxide without a sacrificial reagent on the basis of TCPP in the present disclosure, the TCPP photothermal catalyst has efficient and stable catalytic performance (after the catalyst is continuously used for 24 h, the performance is not significantly reduced). A reaction liquid obtained after a photothermal reaction for 24 h is concentrated by distillation under reduced pressure to obtain commercially available hydrogen peroxide with a concentration of about 3.00 wt %. Therefore, the TCPP photothermal catalyst has a great application prospect.