US20220331775A1

US20220331775A1 - Pyrazole metal complex for absorbing carbon dioxide, method for preparing pyrazole metal complex, and method for absorption of carbon dioxide

Info

Publication number: US20220331775A1
Application number: US17/550,382
Authority: US
Inventors: Yu-Ting Tseng; Tsai-Te LU; Tzu-Chieh YU; Wen-Feng LIAW
Original assignee: National Tsing Hua University NTHU
Current assignee: National Tsing Hua University NTHU
Priority date: 2021-04-12
Filing date: 2021-12-14
Publication date: 2022-10-20
Also published as: US20230241579A1; US12179171B2

Abstract

A pyrazole metal complex for absorption of carbon dioxide, a method for preparing the pyrazole metal complex, and a method for absorbing carbon dioxide are provided; wherein the product produced by reacting pyrazole metal complex and carbon dioxide may be transformed into several economically valuable compounds.

Description

CROSS REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. Provisional Application Ser. No. 63/173,723, filed on Apr. 12, 2021, and the benefit of Taiwan Patent Application Ser. No. 110127682 filed on Jul. 28, 2021. The entirety of each Application is incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a pyrazole metal complex for absorbing carbon dioxide, a method for preparing pyrazole metal complex, and method for absorption of carbon dioxide; particularly, to a pyrazole metal complex for absorbing carbon dioxide in the air, a method for preparing pyrazole metal complex, and method for absorption of carbon dioxide in the air.

2. Description of Related Art

Since the industrial revolution, excessive use of petroleum fuels has caused massive emission of carbon dioxide, which has severely affected the world by causing problems such as the greenhouse effect, seawater acidification, ecological imbalance, and melting icebergs. Accordingly, how to reduce the content of carbon dioxide in the atmosphere and reduce carbon dioxide emissions is an important global issue.
Most of the carbon dioxide capture techniques currently applied in the industry are disadvantageous of oxide sensitive, water sensitive, high volatility, and high demand for renewable energy. Or, the products yield after capturing carbon dioxide are not reusable for synthesizing economically valuable compounds, and can only be stored in the saltwater layer deep underground.
Accordingly, it is desirable to provide a novel carbon dioxide capture technique, which is not sensitive to oxygen or water and the products yielded from capturing carbon dioxide can be converted into other economically valuable compounds. It is also desirable that the compound used for capturing carbon dioxide can be recovered as the original compound and continues to be used to capture carbon dioxide. In this way, the cost of storing the product yield by capturing carbon dioxide can be reduced, and other economically valuable compounds can be synthesized, the compound used to capture carbon dioxide can be reused, and the demand for environmental protection can be met.

SUMMARY OF THE INVENTION

The present invention provides a pyrazole metal complex for absorbing carbon dioxide, wherein the pyrazole metal complex has the structure:
Wherein each of R₁, R₂, and R₃is independently selected from a group consisting of hydrogen, substituted or unsubstituted C₁-C₆alkyl group, and substituted or unsubstituted aryl group; and M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺ [K-18-crown-6 ether]⁺, Mn²⁺, Fe²⁺, Fe²⁺, Co²⁺, Co³⁺, Ni²⁺, Cu²⁺, Cu⁺, and Zn²⁺.
In one embodiment, R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.
In one embodiment, M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.
The present invention also provides a preparing method of the abovementioned pyrazole metal complex, which comprises: step (a): providing a pyrazole compound having the structure:
and step (b): reacting a metal hydride with the pyrazole compound of formula (I-1) to obtain the pyrazole metal complex.
In one embodiment, step (b) further comprises tetrahydrofuran as a solvent.
The present invention further provides a method for absorbing carbon dioxide in the air, comprising: step (1): providing a pyrazole metal complex of formula (I):
wherein each of R₁, R₂, and R₃is independently selected from a group consisting of hydrogen, substituted or unsubstituted C₁-C₆alkyl group, and substituted or unsubstituted aryl group; and M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺, Mn²⁺, Fe²⁺, Fe³⁺, Co²⁺, Co³⁺, Ni²⁺, Cu²⁺, Cu⁺, and Zn²⁺; and step (2): reacting the pyrazole metal complex with carbon dioxide for absorbing carbon dioxide, wherein a product obtained by reacting the pyrazole metal complex and carbon dioxide is a pyrazole amide formate of formula (II):
In one embodiment, R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.
In one embodiment, M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.
In one embodiment, the reaction of the pyrazole metal complex and carbon dioxide is carried out under an inert gas environment in step (2).
The present invention further provides another method for absorbing carbon dioxide, which comprises: step (i): providing a pyrazole metal complex of formula (I)
wherein each of R₁, R₂, and R₃is independently selected from a group consisting of hydrogen, substituted or unsubstituted C₁-C₆alkyl group, and substituted or unsubstituted aryl group; and M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺, Mn²⁺, Fe²⁺, Fe³⁺, Co²⁺, Co³⁺, Ni²⁺, Cu²⁺, Cu⁺, and Zn²⁺; and step (ii): reacting the pyrazole metal complex with carbon dioxide for absorbing carbon dioxide, wherein a product obtained by reacting the pyrazole metal complex and carbon dioxide is a pyrazole amide formate of formula (II):
and step (iii): providing a double nitroso iron complex of formula (III) for reacting with the pyrazole amide formate of formula (II) to obtain a metal complex having the structure of formula (IV):
In one embodiment, in step (i), R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.
In one embodiment, in step (i), M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.
In one embodiment in step (ii), the reaction of the pyrazole metal complex and carbon dioxide is carried out under an inert gas environment.
In one embodiment, the method further comprises a step (iv): providing a calcium trifluoromethanesulfonate (Ca(OTf)₂) for reacting with the metal complex of formula (IV) to obtain a calcium oxalate (CaC₂O₄).
In one embodiment, the method further comprises a step (v): providing a bis(pinacolato)diboron ((PinB)₂) for reacting with the metal complex of formula (IV) to obtain a carbon monoxide.
In one embodiment, the method further comprises a step (vi): providing a 9-Borabicyclo(3.3.1)nonane (9-BBN) for reacting with the metal complex of formula (IV) to obtain a formic acid.
In one embodiment, the method further comprises a step (vii): providing a triethyl boride for reacting with the metal complex of formula (IV) to obtain a propionate.
In one embodiment, the method further comprises a step (viii): providing a zinc trifluoromethanesulfonate for reacting with the metal complex of formula (IV) to obtain a carbon dioxide reduction product.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a ¹³C solid NMR spectrum of Na-pyr of one embodiment of the present invention;

FIG. 2 is a powder X-ray diffraction pattern of Na-pyr and simulated spectrum of one embodiment of the present invention;

FIG. 3 is a ¹³C solid NMR spectrum of K-pyr of one embodiment of the present invention;

FIG. 4 is a powder X-ray diffraction pattern of K-pyr of one embodiment of the present invention;

FIG. 5 is a ¹³C solid NMR spectrum of 18-K-pyr of one embodiment of the present invention;

FIG. 6 is a powder X-ray diffraction pattern of 18-K-pyr and simulated spectrum of one embodiment of the present invention;

FIG. 7 is an IR vibration spectrum of Na-pyr-CO₂of one embodiment of the present invention;

FIG. 8 is a ¹³C solid NMR spectrum of Na-pyr-CO₂of one embodiment of the present invention;

FIG. 9 is a powder X-ray diffraction pattern of Na-pyr-CO₂of one embodiment of the present invention;

FIG. 10 is an IR vibration spectrum of K-pyr-CO₂of one embodiment of the present invention;

FIG. 11 is a ¹³C solid NMR spectrum of K-pyr-CO₂of one embodiment of the present invention;

FIG. 12 is a powder X-ray diffraction pattern of K-pyr-CO₂of one embodiment of the present invention;

FIG. 13 is a schematic diagram of an air capture system of one embodiment of the present invention;

FIG. 14 is a schematic diagram of the detection results of the air capture system of one embodiment of the present invention;

FIG. 15 is a schematic diagram of the detection results of the air capture system of one embodiment of the present invention;

FIG. 16 is a schematic diagram of the detection results of the air capture system of one embodiment of the present invention;

FIG. 17 is a schematic diagram of the detection results of the air capture system of one embodiment of the present invention;

FIG. 18 is a schematic diagram of the detection results of the air capture system of one embodiment of the present invention;

FIG. 19 is an IR vibration spectrum of the product of one embodiment of the present invention;

FIG. 20 is a ¹³C solid NMR spectrum of the product of one embodiment of the present invention;

FIG. 21 is a GC chromatogram of the product of one embodiment of the present invention;

FIG. 22 shows a ¹H NMR spectrum and a ¹³C NMR spectrum of the product of one embodiment of the present invention;

FIG. 23 is a ¹³C NMR spectrum of the product of one embodiment of the present invention;

FIG. 24 is an IR vibration spectrum of the product of one embodiment of the present invention; and

FIG. 25 is a ¹³C NMR spectrum of the product of one embodiment of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Hereafter, examples will be provided to illustrate the embodiments of the present invention. The advantages and effects of the invention will become more apparent from the disclosure of the present invention. Other various aspects also may be practiced or applied in the invention, and various modifications and variations can be made without departing from the spirit of the invention based on various concepts and applications.
[Synthesis and Identification of the Pyrazole Metal Complex]
Firstly, reaction formula (a) is carried out by reacting sodium with pyrazole:
The product synthesized by the above reaction is identified as sodium pyrazolate (Na-pyr) according to the chemical shift (108.58/144.28 ppm) of the ¹³C solid NMR spectrum (FIG. 1), and comparison between the powder X-ray diffraction pattern of the product and simulated spectrum (FIG. 2).
Reaction formula (b) is carried out by reacting potassium hydride with pyrazole:
The product synthesized by the above reaction is identified as potassium pyrazolate (K-pyr) according to the chemical shift (111.19/139.35 ppm) of the ¹³C solid NMR spectrum (FIG. 3), and the powder X-ray diffraction pattern of the product (FIG. 4) supports that the product has an orderly arrangement.
Further, reaction formula (C) is carried out by reacting potassium hydride and 18-crown-6 ether with pyrazole:
The product synthesized by the above reaction is identified as [K-18-crown-6-ether][pyr](18-K-pyr) according to the chemical shift (70.92, 100.66, 136.190 ppm) of the ¹³C solid NMR spectrum (FIG. 5), and comparison between the powder X-ray diffraction pattern of the product and simulated spectrum (FIG. 6)
[Reaction of Pyrazole Metal Complex with Carbon Dioxide]
Firstly, reaction formula (d) is carried out by reacting Na-pyr with carbon dioxide:
The reaction product Na-Pyr-CO₂is identified according to the IR vibration spectrum (1716 cm⁻¹) (FIG. 7) and the chemical shift (152.64, 138.80, 132.43, and 106.5 ppm) of the ¹³C solid NMR spectrum (FIG. 8). Also, an orderly arrangement of the product is supported by the powder X-ray diffraction pattern (FIG. 9).
Reaction formula (e) is carried out by reacting K-pyr and carbon dioxide:
The reaction product K-Pyr-CO₂is identified according to the IR vibration spectrum (1690 cm-1) (FIG. 10) and the chemical shift (151.89, 140.02, 130.44, and 105.97 ppm) of the ¹³C solid NMR spectrum (FIG. 11). Also, an orderly arrangement of the product is supported by the powder X-ray diffraction pattern (FIG. 12).
[Pyrazole Metal Complex for the Capture of Carbon Dioxide]
An air capture system 1000 illustrated in FIG. 13 is provided for testing the carbon dioxide capture ability of the pyrazole metal complex. The air capture system 1000 mainly includes an air compressor 1, a flow controller 2, a tubing 3, a sample column 4, a drying tube 5, a flow detector 6, and a gas chromatograph 7. The air output by the air compressor 1 is controlled at a flow rate of 200 mL/min by the flow controller 2 and passes through the tubing 3 contained with water so that the air is humidified. Next, the air passes through the sample column 4 filled with different pyrazole metal complexes whilst the pyrazole metal complex in the sample column captures the carbon dioxide in the air. After carbon dioxide is captured from the air by different pyrazole metal complexes and water is removed from the air by the drying tube 5, the air flows into the gas chromatograph 7 for detection of the concentration of carbon dioxide.
First, the above-mentioned air capture procedure is performed with the sample column 4 filled with Na-pyr. Dry air and humidified air are independently provided and the detection results are shown in FIG. 14. According to the results shown in FIG. 14, Na-pyr can capture 80 percent of the carbon dioxide for 20 minutes and capture 50 percent of the carbon dioxide for 160 minutes whilst the air is humidified. However, the ability to capture carbon of the pyrazole metal complexes in dry air dioxide is poor.
Next, the air capture procedure is performed with the sample column 4 filled with Na-3-methylpyrazolate (Na-3-mpyr) with a methyl substituent at position 3. Humidified air is provided and the detection result is shown in FIG. 15. According to the result shown in FIG. 15, Na-3-mpyr has the ability to capture carbon dioxide from the humidified air.
Furthermore, the air capture procedure is performed with the sample column 4 filled with K-pyr. Dry air and humidified air are provided and the detection result is shown in FIG. 16. According to the result shown in FIG. 16, K-pyr can capture 20 percent of the carbon dioxide for 60 minutes from the humidified air; K-pyr also has the ability to capture carbon dioxide in dry air.
Next, the air capture procedure is performed with the sample column 4 filled with K-3-methylpyrazolate (K-3-mpyr) with a methyl substituent at position 3. Humidified air is provided and the detection result is shown in FIG. 17. According to the result shown in FIG. 17, K-3-mpyr has the ability to capture carbon dioxide from the humidified air.
Furthermore, the air capture procedure is performed with the sample column 4 filled with 18-K-pyr. Dry air and humidified air are provided and the detection result is shown in FIG. 18. According to the result shown in FIG. 18, 18-K-pyr can capture over 95 percent of the carbon dioxide for 20 minutes from the humidified air and the dry air.
According to the test results, each of pyrazole metal complexes including Na-pyr, Na-3-mpyr, K-pyr, K-3-mpyr, and 18-K-pyr has the ability to capture carbon dioxide in the air.
The product obtained after capturing carbon dioxide by the pyrazole metal complex can be further combined with different chemical reagents to reduce carbon dioxide into economically valuable products.
[Conversion of Carbon Dioxide to Calcium Oxalate]
The product of Na-3-mpyr or K-3-mpyr capturing carbon dioxide is shown in formula (II-1):
Next, reacting the product (II-1) with the double nitroso iron complex of formula (III) to obtain a metal complex of formula (IV-1):
Furthermore, reacting the metal complex 2CO₂of formula (IV-1) with the calcium trifluoromethanesulfonate (Ca(OTf)₂), the product is characterized by the IR absorption peak at 1657 cm′ (FIG. 19). The absorption peak of the product obtained by reacting 2-¹³CO₂is shifted to 1633 cm′ (FIG. 19). According to the IR vibration spectrum, the formation of the carbon dioxide reduction product is confirmed. In addition, the carbon dioxide reduction product is also confirmed by the chemical shift 161.99 ppm in the NMR spectrum (FIG. 20).
[Conversion of Carbon Dioxide to Carbon Monoxide]
Similarly, reacting the product (II-1) of Na-3-mpyr or K-3-mpyr capturing carbon dioxide with the double nitroso iron complex of formula (III) to obtain a metal complex of formula (IV-1). Then, reacting the metal complex 2-CO₂and bis(pinacolato)diboron, the air after the reaction is collected and is confirmed by the gas chromatograph that the reaction converts carbon dioxide into carbon monoxide (FIG. 21).
[Conversion of Carbon Dioxide to Formic Acid]
Similarly, the product collected by reacting the metal complex 2-CO₂represented by formula (IV-1) with 9-borabicyclo(3.3.1)nonane is dissolved in heavy water. It is confirmed that the reaction converts carbon dioxide into formate by the chemical shift 8.42 ppm in ¹H NMR spectrum and 171.62 ppm in ¹³C NMR spectrum (FIG. 22).
[Conversion of Carbon Dioxide to Propionate]
Similarly, reacting the product (II-1) of Na-3-mpyr or K-3-mpyr capturing carbon dioxide with the double nitroso iron complex of formula (III) to obtain a metal complex of formula (IV-1).
The product of reacting the metal complex 2-¹³CO₂with triethyl boride is dissolved in heavy water. It is confirmed that the reaction converts carbon dioxide into propionate by the chemical shift 165.28 ppm in ¹³C NMR spectrum (FIG. 23).
[Capture and Purification of Carbon Dioxide]
The product obtained by reacting metal complex 2-CO₂represent by formula (IV-1) with zinc trifluoromethanesulfonate is characterized by the IR absorption peaks at 1250 cm⁻¹and 1176 cm⁻¹(FIG. 24). When 2-¹³CO₂is used, the IR absorption peaks shift to 1225 cm⁻¹and 1154 cm⁻¹(FIG. 24). According to the IR vibration spectrum, the formation of the carbon dioxide reduction product is confirmed. Also, it is confirmed that the reaction converts carbon dioxide into a carbon dioxide reduction product by the chemical shift 66.4 ppm and 65.6 ppm in ¹³C NMR spectrum (FIG. 25) when 2-¹³CO₂is used.
[Reduction of the Pyrazole Metal Complex]
After the pyrazole metal complex captures carbon dioxide, reacts with the double nitroso iron complex represented by formula (III), and further reacts with calcium triflate to form calcium oxalate, the side product obtained can further react with protonated pentamethyldiethylenetriamine (PMDTA) to form a pyrazole compound and the double nitroso iron complex represented by formula (III), wherein the pyrazole can further convert into the pyrazole metal complex of the present invention. That is, the pyrazole metal complex of the present invention and the double nitroso iron complex can be recovered after the capture of CO₂and forming calcium oxalate.
In summary, the pyrazole metal complex of the present invention is capable of capturing carbon dioxide efficiently, the product yields after capturing carbon dioxide can be converted to several economically valuable compounds such as carbon monoxide, calcium oxalate, formate, and propionate, or can be converted to carbon dioxide reduction product through reactions. Also, the pyrazole metal complex and the double nitroso iron complex required in the reaction can further be recovered and reused, which meets the requirements of low cost and environmental friendly.

Claims

1. A pyrazole metal complex for absorbing carbon dioxide, having the structure:

wherein each of R₁, R₂, and R₃is independently selected from a group consisting of hydrogen, substituted or unsubstituted C₁-C₆alkyl group, and substituted or unsubstituted aryl group; and

M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺, Mn²⁺, Fe²⁺, Fe³⁺, Co²⁺, Co³⁺, Ni²⁺, Cu²⁺, Cu⁺, and Zn²⁺.

2. The pyrazole metal complex of claim 1, wherein R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.

3. The pyrazole metal complex of claim 1, wherein M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.

4. A preparing method of the pyrazole metal complex of claim 1, comprising the steps of:

step (a): providing a pyrazole compound having the structure:

and

step (b): reacting a metal hydride with the pyrazole compound of formula (I-1) to obtain the pyrazole metal complex.

5. The preparing method of claim 4, wherein step (b) further comprising a tetrahydrofuran as a solvent.

6. A method for absorbing carbon dioxide, comprising:

step (1): providing a pyrazole metal complex of formula (I):

M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺, Mn²⁺, Fe²⁺, Fe³⁺, Co²⁺, Co³⁺, Ni²⁺, Cu²⁺, Cu⁺, and Zn²⁺; and

step (2): reacting the pyrazole metal complex with carbon dioxide for absorbing carbon dioxide, wherein a product obtained by reacting the pyrazole metal complex and carbon dioxide is a pyrazole amide formate of formula (II):

7. The method of claim 6, wherein step (1), R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.

8. The method of claim 6, wherein step (1), M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.

9. The method of claim 6, wherein step (2), the reaction of the pyrazole metal complex and carbon dioxide is carried out under an inert gas environment.

10. method for absorbing carbon dioxide, comprising:

step (i): providing a pyrazole metal complex of formula (I)

step (ii): reacting the pyrazole metal complex with carbon dioxide for absorbing carbon dioxide, wherein a product obtained by reacting the pyrazole metal complex and carbon dioxide is a pyrazole amide formate of formula (II):

and

step (iii): providing a double nitroso iron complex of formula (III) for reacting with the pyrazolamide formate of formula (II) to obtain a metal complex having structure of formula (IV):

11. The method of claim 10, wherein step (i), R₁is selected from a group consisting of hydrogen, methyl group, and benzyl group; each of R₂and R₃is independently hydrogen.

12. The method of claim 10, wherein step (i), M₁ ⁿ⁺ is selected from a group consisting of Na⁺, K⁺, and [K-18-crown-6 ether]⁺.

13. The method of claim 10, wherein step (ii), the reaction of the pyrazole metal complex and carbon dioxide is carried out under an inert gas environment.

14. The method of claim 10, further comprising:

step (iv): providing a calcium trifluoromethanesulfonate (Ca(OTf)₂) for reacting with the metal complex of formula (IV) to obtain a calcium oxalate (CaC₂O₄).

15. The method of claim 10, further comprising:

step (v): providing a bis(pinacolato)diboron ((PinB)₂) for reacting with the metal complex of formula (IV) to obtain a carbon monoxide.

16. The method of claim 10, further comprising:

step (vi): providing a 9-Borabicyclo(3.3.1)nonane (9-BBN) for reacting with the metal complex of formula (IV) to obtain a formic acid.

17. The method of claim 10, further comprising:

step (vii): providing a triethyl boride for reacting with the metal complex of formula (IV) to obtain a propionate.

18. The method of claim 10, further comprising:

step (viii): providing a zinc trifluoromethanesulfonate for reacting with the metal complex of formula (IV) to obtain a carbon dioxide reduction product.