COMPOSITION AND METHOD FOR CATALYTIC REDUCTION OF CARBON DIOXIDE OR CARBOHYDRATE

Abstract

Embodiments of the present invention relates to integrated catalyst systems and associated processes that directly converts carbon dioxide or carbohydrate to CO, methane, or other valuable chemicals at room temperature and atmospheric pressure, requiring no extra energy. The integrated catalyst systems are comprised of nitrogenous heterocyclic compounds and at least two metal elements, wherein one metal element needs to be active than the other one. The integrated catalyst systems can be applied to reduce carbon dioxide and carbohydrate at room temperature with considerable conversion efficiency. The reduction process involves the steps of: a) nitrogenous heterocyclic compounds performance as solvent/major catalyst, dual component as reducing agent / co-catalyst; b) introducing the above integrated catalysts into the reactor full of CO.sub.2 or carbohydrate, and keeping stirring the reacting system for 1 to 4 hours, without any illumination or heating; c) CO, methane, or other reduction product is achieved with a conversion efficiency of about 100%; d) the reduction products are gases, which can be directly separated from the system without any additional separation process or involving additional chemicals.

Claims

1. A composition for catalytic reduction of carbon dioxide or carbohydrates comprising a nitrogen heterocyclic compound and at least two metal elements, wherein, a first metal element, performing as a reactant, has more reactivity than a second metal element which acts as co-catalyst.

2. The composition according to claim 1, wherein the nitrogen heterocyclic compound is at least one of the following: imidazole, 1-methylimizazole, 1-ethylimizazole, 1-ethyul-3-methylimidazolium tetrafluroborate salt, 4-methylimidazole, 1-allyimidazole, 2-methylimidazole, 1-butyl-3-methyl imidazolium bromide salt, 1-benzylimidazole, histamine, 1-butylimidazole, acetonitrile(1-imidazole group), 1,2-dimethylimidazole, 1-acetylimidazole, and 1,2,4-triazole.

3. The composition according to claim 1, wherein the two metal elements are different.

4. The composition according to claim 2, wherein, the second metal element, acting as the co-catalyst, is one of the following metal elements: tin, copper, silver, nickel, cadmium, cobalt and lead.

5. The composition according to claim 2, wherein, the first metal element, acting as the reactant, is one of the following metal elements: zinc, iron, aluminum, manganese, magnesium, nickel, tin.

6. A method of using the composition metal according to claim 1 for catalytic reduction of carbon dioxide or carbohydrates.

7. A method of using the composition metal comprising the step of: mixing a substrate with the composition of claim 1, reacting to convert CO.sub.2 and carbohydrate to CO and methane.

8. The method according to claim 7, wherein, the nitrogen heterocyclic compound is solid under room temperature, dissolving the nitrogen heterocyclic compound in a solvent.

9. The method according to claim 8, wherein the solvent is water, methanol, or ethanol.

10. The method according to claim 7, wherein, CO.sub.2 is pure CO.sub.2 or waste gas containing carbon dioxide.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0030] FIG. 1 illustrates the gas chromatogram of the cylinder gas before the reaction in embodiment 1, wherein, (a) is the gas chromatogram of the standard gas consisting of 2000ppm carbon monoxide, 2000ppm methane, and 2000ppm carbon dioxide; (b) gas chromatogram of the gas in the bottle before reaction.

[0031] FIG. 2 shows the detection results of the gas in the bottle after the reaction in Embodiment 1, wherein (a) is the gas chromatogram of the gas in the bottle after the reaction, and (b) is the combustion diagram of the gas in the bottle.

[0032] FIG. 3 shows the free radical signal diagram of catalyst M.sub.1 and ImZ in embodiment 1, wherein (a) is the free radical signal diagram after M.sub.1 reacts with ImZ, and (b) is the free radical signal diagram after M.sub.1 reacts with ImZ and carbon dioxide is introduced.

[0033] FIG. 4 shows the XRD results of the reaction products in embodiment 1.

[0034] FIG. 5 shows the crystal structure of the reaction product in embodiment 1.

[0035] FIG. 6 illustrates the gas detection results in the bottle after reaction in Embodiment 2, wherein, (a) is the gas chromatogram after reaction with ionic liquid, and (b) is the combustion diagram of the gas in the bottle.

[0036] FIG. 7 summarizes a schematic diagram of carbon dioxide reduction by imidazole + bimetal system

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0037] Reactor: In the experiment, an air-tight reaction flask with a volume of one liter was used as the reactor for the catalytic reduction reaction.

Embodiment 1: Reducing Carbon Dioxide to Produce Carbon Monoxide

[0038] At room temperature, 60 milliliter of 1-methylimidazole, 2.5 gram of zinc powder and 0.5 gram of copper powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, keep introducing ultra pure CO.sub.2 (99.999%) into the flask until the pressure in the flask approached 0.1 - 0.3 MPa, then the flask was closed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min (FIG. 1b), the gas was identified as carbon dioxide by comparison with the standard gas (FIG. 1a). Then the switch of mini fountain pump was turned on, wherein the imidazole suspension with metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, the gas in the flask was extracted for GC analysis. The chromatographic peak was found appearing near t=0.9 min (FIG. 2a), while the chromatographic peak near t=4.5 min (the characteristic peak for CO.sub.2) disappeared completely, suggesting that CO.sub.2 was converted to carbon monoxide. Moreover, the carbon monoxide gas burned violently (FIG. 2b) and emitted a blue flame characteristic of carbon monoxide. Combustion experiments further confirmed that the innovative system can efficiently and completely reduce carbon dioxide, and the converted carbon monoxide can be applied as fuel.

[0039] FIG. 3 (a) shows the free radical signal obtained by analyzing EPR of the stirred solution of 1-methylimidazole and copper powder with DMPO trapping agent; (b) the free radical signal obtained by analyzing EPR of the stirred mixture of 1-methylimidazole and copper powder with carbon dioxide injected into the solution and DMPO trapping agent added to solution. (Beijing E Testing Company is commissioned to conduct analysis)

TABLE-US-00001 Organic Element Analysis (C, N, H) sample weight (mg) method C [%] N [%] H [%] Guide sample: Sulfanilamide 3.0480 2 mg 80 s 41.81 16.25 4.650 Test #1 2.6300 2 mg 80 s 34.13 17.38 4.117 Test #2 2.8200 2 mg 80 s 34.17 17.33 4.100

TABLE-US-00002 Element Oxygen (O) Analysis sample weight (mg) method O [%] Guide sample: Benzoic acid) 2.2330 CO-IRMS 26.200 Test #1 3.4220 CO-IRMS 25.106 Test #2 3.6380 CO-IRMS 25.165

FIG. 4 illustrates the XRD diffraction patterns of the product (white powder) of the reaction, and table 1 and table 2 (test #1 and test #2 are the repeated test for the same sample) (Beijing E Testing Company is commissioned to conduct analysis).

Embodiment 2: Reducing Carbon Dioxide to Produce Methane

[0040] At room temperature, the ionic liquid (60 milliliter of 1-ethyul-3-methylimidazolium tetrafluroborate salt, 2.5 gram of zinc powder and 0.5 gram of copper powder) was put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, keep introducing ultra pure CO.sub.2 (99.999%) into the flask until the pressure in the flask approached 0.1 - 0.3MPa, then the flask was closed. When the gas in the bottle was confirmed to be pure carbon dioxide analyzed by gas chromatography, a mini fountain pump was switched on, wherein the ionic liquid was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 3 hours, the gas in the flask was extracted for GC analysis. The chromatographic peak was found appearing near t=2.2 min (FIG. 6a), while the chromatographic peak near t=4.5 min (the characteristic peak for CO.sub.2) disappeared completely, suggesting that CO.sub.2 is converted to methane. Moreover, the methane gas burned violently (FIG. 6b) and emitted a blue flame characteristic of methane. Combustion experiments further confirmed that the innovative liquid system (1-ethyul-3-methyliminazolium tetrafluroborate salt + copper + zinc) can efficiently and completely reduce carbon dioxide, and the converted methane can be applied as fuel.

Embodiment 3: Reduction of Carbon Dioxide to Produce a Mixture of Carbon Monoxide and Methane

[0041] At room temperature, 60 milliliter of methanol, 8 gram of imidazole, 2.5 gram of zinc powder and 0.1 gram of silver powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, keep introducing ultra pure CO.sub.2 (99.999%) into the flask until the pressure in the flask approaches 0.1 - 0.3MPa, then close the flask. When the gas in the bottle was confirmed to be pure carbon dioxide analyzed by gas chromatography, switch on mini fountain pump, wherein the ionic liquid was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions take place. After continuous reaction for 3 hours, the gas in the flask was extracted for GC analysis. The chromatographic peaks were identified appearing near t=0.9 min and t=2.2 min respective, while the chromatographic peak near t=4.5 min (the characteristic peak for CO.sub.2) disappeared completely, suggesting that CO.sub.2 was converted to carbon monoxide and methane, wherein carbon monoxide was the major component which amounts to 70% of the products.

Embodiment 4: Other Nitrogen-Containing Heterocyclic Compounds + Bimetallic Systems

[0042] Besides the above embodiment about the catalytic reduction of CO.sub.2, Other similar imidazole + bimetallic systems also reduced carbon dioxide at room temperature to carbon monoxide, methane, or a combination of thereof, wherein the specific reactants, catalysts and productions are listed in table 3 (note: since 1-methyliminazole, 1-ethyliminazole, and ionic liquid of 1-butyl-3-methyl iminazolium bromide salt are in a liquid state themselves, these reaction system need no methanol, ethanol as solvent) .

[0042] TABLE-US-00003 Imidazole with bimetallic and the catalytic reduction product of carbon dioxide and carbohydrates Imidazole and its derivatives Solvent Metal 1 (M.sub.1) Metal 2 (M.sub.2) Product Imidazole (8 g) Ethanol (mL) Sn powder (0.5 g) Zn powder (2.5 g) CO 1-ethyliminazole(60ml) Cu powder (0.5 g) Zn powder (2.5 g) CO 1-methyliminazole(60ml) Ag powder (0.5 g) Fe powder (2.5 g) CO+CH.sub.4 4-methyliminazole(60ml) ethanol (mL) Cu powder (0.5 g) Fe powder (2.5 g) CO 1-allyiminazole (60ml) -- Ni powder (0.5 g) Al powder (2.5 g) CO 1-ethyliminazole (60ml) -- Pb powder (0.5 g) Mn powder (2.5 g) CH.sub.4 1-methyliminazole(60ml) -- Cu powder (0.5 g) Fe powder (2.5 g) CO 1-methyliminazole(60ml) -- Cu powder (0.5 g) Al powder (2.5 g) CO 1-methyliminazole(60ml) -- Cu powder (0.5 g) Mg powder (2.5 g) CO 1-methyliminazole(60ml) -- Ag powder (0.5 g) Fe powder (2.5 g) CO 1-methyliminazole(60ml) -- Ag powder (0.5 g) Zn powder (2.5 g) CO 1-methyliminazole(60ml) -- Ag powder (0.5 g) Al powder (2.5 g) CO 2-methyliminazole(8 g) methanol (mL) Cu powder (0.5 g) Al powder (2.5 g) CH.sub.4 1-butyl-3-methyl iminazolium bromide salt (60ml) -- Co powder (0.5 g) Al powder (2.5 g) CO+CH.sub.4 1-ethyul-3-methyliminazolium tetrafluroborate salt(60ml) -- Ag powder (0.5 g) Zn powder (2.5 g) CO+CH.sub.4 1,2,4-triazole (8 g) ethanol (mL) Sn powder (0.5 g) Al powder (2.5 g) CO 1-benzyliminazole (8 g) methanol (mL) Ag powder (0.5 g) Mn powder (2.5 g) CH.sub.4 Histamine (8 g) ethanol (mL) Cu powder(0.5 g) Fe powder (2.5 g) CO+CH.sub.4 1-benzyliminazole (8 g) methanol (mL) Ag powder (0.5 g) Al powder (2.5 g) CO 1-butyliminazole (8 g) ethanol (60ml) Ag powder (0.5 g) Mn powder (2.5 g) CO acetonitrile (1-iminazole group) (8 g) methanol (mL) Pb powder (0.5 g) Zn powder (2.5 g) CH.sub.4 1,2-dimethylimidazole (8) H.sub.2O (mL) Ni powder (0.5 g) Fe powder (2.5 g) CO+CH.sub.4 1-acetylimidazole (8 g) H.sub.2O (mL) Co powder (0.5 g) Fe powder (2.5 g) CO

Embodiment 5: Capturing of Carbon Dioxide and Its Conversion In-Situ

[0043] Flue gas emitted from on-site plants (power plants, aluminum plants, cement plants, etc.) was generally a mixture of carbon dioxide, oxygen and nitrogen, wherein the content of carbon dioxide was about 15%. Super pure carbon oxide was achieved through adsorption, desorption, and compression which involve high press condition and energy consuming process. If the carbon oxide capture and its reduction and conversion can be integrated, it will not only be desirable to reduce the equipment cost and energy consumption, but also accomplish the catalytic reduction and conversion of carbon dioxide economically at room temperature and atmosphere pressure. The present invention describes the imidazole+bimetallic system which demonstrate excellent selectivity and rapid adsorption of carbon oxide, wherein the integrated catalytic reduction system of 1-methyliminazole+Cu+Zn was applied in the capturing of carbon dioxide and its conversion in-situ. At room temperature, 60 milliliter of 1-methylimidazole, 2.5 gram of zinc powder and 0.5 gram of copper powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then simulated flue gas (15% of carbon oxide and 85% of oxygen) was introduced into the imidazole+bimetallic system by bubbling, chromatorgraphic analysis data indicated that 90% of carbon dioxide of the flue gas can be adsorbed by the imidazole+bimetallic system. When the introducing of flue gas was finished, the oxygen in the flask was removed by vacuuming to make sure that the converted product was free of oxygen. Then the switch of mini fountain pump was turned on, wherein the imidazole suspension with metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, the gas in the flask was extracted for GC analysis, and the chromatographic analysis data demonstrate that 100% of carbon monoxide filled with the flask, which suggests carbon dioxide was converted with high efficiency and selectivity. This innovative process avoids the adsorption and desorption steps, and make sure that the economically integrated of adsorption and conversion of carbon oxide.

Embodiment 6: Conversion of Carbohydrate to Carbon Monoxide

[0044] Besides the conversion of carbon oxide to carbon monoxide or methane, natural carbohydrates such as glucose and cellulose can be converted to desired fuel and economical chemical reagents.

[0045] At room temperature, 30 milliliter of 1-methylimidazole, 1 milliliter of H.sub.2O, 2.5 gram of zinc powder,0.5 gram of copper powder, and 3 gram of glucose (or sucrose, starch, cellulose) were put into a one liter flask. The air in the flask was removed completely by vacuumizing, then the switch of magnetic stirrer was turned on, and series chemical reactions took place. After continuous reaction for 4 hours, the gas in the flask was extracted for GC analysis, and the chromatographic analysis data demonstrate that glucose, sucrose, starch and cellulose can be converted to carbon monoxide, wherein the conversion efficiency of glucose to carbon monoxide ranks first, with its maximum concentration of carbon monoxide approaching 10.sup.5 ppm.

[0046] The embodiment was an indirect utilization of carbon dioxide, wherein carbon dioxide was firstly converted to carbohydrate in chloroplast of green leaves through photosynthesis, then with the innovative catalytic reduction process, the synthesized carbohydrate was converted to energy materials or bio-diesel.

Embodiment 7: Imidazole+Copper Catalytic System

[0047] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of copper powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, 4 hours, and 8 hours respectively the gas in the flask was extracted for GC analysis, and the chromatographic peak still appeared around t = 4.5 min, which suggests no conversion of carbon dioxide in the flask.

Embodiment 8: Imidazole+Nickel Catalytic System

[0048] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of nickel powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, 4 hours, and 8 hours respectively the gas in the flask was extracted for GC analysis, and the chromatographic peak still appeared around t = 4.5 min, which suggests no conversion of carbon dioxide in the flask.

Embodiment 9: Imidazole+Silver Catalytic System

[0049] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 1 gram of silver powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, 4 hours, and 8 hours respectively the gas in the flask was extracted for GC analysis, and the chromatographic peak still appeared around t = 4.5 min, which suggests no conversion of carbon dioxide in the flask.

Embodiment 10: Imidazole+Cobalt Catalytic System

[0050] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of cobalt powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, 4 hours, and 8 hours respectively the gas in the flask was extracted for GC analysis, and the chromatographic peak still appeared around t = 4.5 min, which suggests no conversion of carbon dioxide in the flask.

Embodiment 11: Imidazole+Tin Catalytic System

[0051] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of tin powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, 4 hours, and 8 hours respectively the gas in the flask was extracted for GC analysis, and the chromatographic peak still appeared around t = 4.5 min, which suggests no conversion of carbon dioxide in the flask.

Embodiment 12: Imidazole+Zinc Catalytic System

[0052] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of zinc powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, the gas in the flask was extracted for GC analysis, and the chromatographic peaks appeared around t = 0.9 min and t = 4.5 min respectively, which suggests 7.5% of conversion rate of carbon dioxide to carbon monoxide in terms of the calculation the chromatographic peak area. The conversion rate of carbon dioxide to carbon monoxide approaches 35% when the system was continuously mixed for 24 hours in the flask.

Embodiment 13: Imidazole+Aluminum Catalytic System

[0053] At room temperature, 60 milliliter of 1-ethylimidazole (or imidazole, 2-methylimidazole, 1-allyiminazole, 1-ethyul-3-methyliminazolium tetrafluroborate salt) and 2 gram of aluminum powder were put into a one liter reaction flask. The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, the gas in the flask was extracted for GC analysis, and the chromatographic peaks appeared around t = 2.2 min and t = 4.5 min respectively, which suggests 3.8% of conversion rate of carbon dioxide to methane in terms of the calculation the chromatographic peak area. The conversion rate of carbon dioxide to methane approaches 16.6% when the system was continuously mixed for 24 hours in the flask.

Embodiment 14 a Series of Imidazole+Bimetallic Catalytic System (Illustrates as Table 4) With Different Metallic Proportion

[0054] At room temperature, 60 milliliter of 1-methylimidazole and certain grams of metal #1(M.sub.1) and metal #2 (M.sub.2) (with different proportions of the two metals, shown in Table 4) were put into a one liter reaction flask.

[0054] TABLE-US-00004 the effect of metallic proportion on the conversion of carbon dioxide (reaction temperature: room temperature; reaction time: 2 hours) No. M.sub.1 M.sub.2 M.sub.1/M.sub.2 CO.sub.2 conversion 1 Cu powder (10 g) Fe powder (2.5 g) 4:1 99.23 % 2 Cu powder (5 g) Fe powder (2.5 g) 2:1 99.98 % 3 Cu powder (2.5 g) Fe powder (2.5 g) 1:1 99.91 % 4 Cu powder (0.5 g) Fe powder (2.5 g) 1:5 99.92 % 5 Cu powder (0.25 g) Fe powder (2.5 g) 1:10 99.87 % 6 Cu powder (0.25 g) Fe powder (5 g) 1:20 99.65 % 7 Cu powder (0.25 g) Fe powder (10 g) 1:40 99.42 % 8 Cu powder (0.25 g) Fe powder (20 g) 1:80 99.33 % 9 Cu powder (0.25 g) Fe powder (25 g) 1:100 99.53 % 10 Cu powder (0.25 g) Fe powder (50 g) 1:200 99.68 % 11 Cu powder (10 g) Zn powder (2.5 g) 4:1 99.74 % 12 Cu powder (5 g) Zn powder (2.5 g) 2:1 99.13 % 13 Cu powder (2.5 g) Zn powder (2.5 g) 1:1 99.34 % 14 Cu powder (0.5 g) Zn powder (2.5 g) 1:5 99.26 % 15 Cu powder (0.25 g) Zn powder (2.5 g) 1:10 99.45 % 16 Cu powder (0.25 g) Zn powder (5 g) 1:20 99.88 % 17 Cu powder (0.25 g) Zn powder (20 g) 1:80 99.95 % 18 Cu powder (0.25 g) Zn powder (25 g) 1:100 99.36 % 19 Cu powder (0.25 g) Zn powder (50 g) 1:200 99.23 % 20 Ag powder (10 g) Zn powder (2.5 g) 4:1 99.17 % 21 Ag powder (2.5 g) Zn powder (2.5 g) 1:1 99.85 % 22 Ag powder (0.5 g) Zn powder (2.5 g) 1:5 99.39 % 23 Ag powder (0.25 g) Zn powder (2.5 g) 1:10 99.50 % 24 Ag powder (0.1 g) Zn powder (25 g) 1:250 99.76 %

[0055] The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3 MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 2 hours, the gas in every flask was extracted for GC analysis, and the chromatographic peaks appeared around t = 0.9 min and t = 4.5 min respectively, which illustrates n% of conversion rate of carbon dioxide to methane in terms of the calculation the chromatographic peak area, (as illustrated in table 4), which suggests the proportion of two metals applied in the above reaction performing no effect on the catalytic effect of the imidazole+bimetallic in the reduction of carbon dioxide.

Embodiment 15: Series of Bimetallic+Imidazole Catalytic Systems With Different Concentration of Solid Imidazole

[0056] At room temperature, 60 milliliter of ethanol, n gram of 4-methylimidazole (the value of n was listed in table 5), 0.1 or 0.5 gram of metal #1(M.sub.1) and 2.5 gram of metal #2 (M.sub.2) were put into a one liter reaction flask. The catalytic systems comprise of 2.5 gram of M.sub.1, 0.1 gram of M.sub.2, and different gram of 4-methylimidazole which is illustrated in table 5.

[0056] TABLE-US-00005 The effect of concentration of imidazole compound on the conversion rate of carbon oxide (reaction temperature, room temperature; reaction time, 2 hours) No. imidazole solvent Metal #1 (M.sub.1) Metal #2 (M.sub.2) CO.sub.2 conversation rate 1 4-methylimidazole (5 g) Ethanol(mL) Ag powder (0.1 g) Mg powder (2.5 g) 26.45 % 2 4-methylimidazole (10 g) Ethanol(mL) Ag powder (0.1 g) Mg powder (2.5 g) 27.00 % 3 4-methylimidazole (20 g) Ethanol(mL) Ag powder (0.1 g) Mg powder (2.5 g) 26.32 % 4 4-methylimidazole (4 g) Ethanol(mL) Ag powder (0.1 g) Mg powder (2.5 g) 25.97 % 5 4-methylimidazole (5 g) Ethanol(mL) Co powder (0.5 g) A1 powder (2.5 g) 13.35 % 6 4-methylimidazole (10 g) Ethanol(mL) Co powder (0.5 g) A1 powder (2.5 g) 14.54 % 7 4-methylimidazole (20 g) Ethanol(mL) Co powder (0.5 g) A1 powder (2.5 g) 13.70 % 8 4-methylimidazole (40 g) Ethanol(mL) Co powder (0.5 g) A1 powder (2.5 g) 13.20 %

[0057] The air in the flask was removed completely by vacuumizing, then super pure carbon dioxide (99.999% of carbon oxide) was being introduced into the flask until the intensity of pressure approaches 0.1 - 0.3MPa, and the flask was sealed. The gas chromatographic instrument was applied to analyze the composition in the flask, the chromatographic peak appeared around t = 4.5 min, the gas in the flask was identified as carbon dioxide by comparison with the standard gas. The switch of mini fountain pump was turned on, wherein the imidazole suspension with mono-metallic power was scattered in the flask and thoroughly mixed with CO.sub.2, and series chemical reactions took place. After continuous reaction for 3 hours, the gas in every flask was extracted for GC analysis, and the chromatographic peaks appeared around t = 2.2 min and t = 4.5 min respectively, which illustrates n% of conversion rate of carbon dioxide to carbon monoxide in terms of the calculation the chromatographic peak area, wherein n ranges from 13.20 to 27.00 (as illustrated in table 5), which suggests that the concentration of solid imidazole dissolved in ethanol plays no significant effect on the catalytic effect in the carbon oxide reduction.

Embodiment 16: Reaction Mechanism

[0058] Taking imidazole compounds as an example, the reaction mechanism of the present invention is as follows: imidazoline compounds (imidazoline, abbreviated as ImZ) are compounds with aromatic structure characteristics and have the ability to accept electrons. When ImZ is in contact with some metal M.sub.1, electron transfer can occur between them (FIG. 7), imidazole is an electron acceptor, and metal is an electron donor. After the charge transfer, a charge transfer complex is formed in the system, and imidazole becomes a negatively charged anion [ImZ] Θ with high activity, and its free radical signal is shown in FIG. 3a (detection results in Example 1). The carbon atoms in carbon dioxide have an electron-deficient structure, so [ImZ] Θ will activate carbon dioxide molecules to form carbon dioxide anion radicals (FIG. 3b, the detection results in Example 1). The free radical continues to get an electron from another more active metal M.sub.2 in the system, and finally disproportionates into a carbon monoxide molecule and a carbonate ion. Carbonate and ImZ and metal M.sub.2 generate M.sub.2CO.sub.3 (ImZ) x (x=1, 2, 3), for example, the reaction product in Example 1 is Zn (CO.sub.3) (C.sub.4N.sub.2H.sub.6).sub.2•2H.sub.2O (FIG. 5). The generated carbon monoxide molecules may continue to undergo the (6H.sup.+, 6e.sup.-) process until methane molecules are generated. The catalytic principles of other nitrogen-containing heterocyclic compounds are similar.

[0059] The reaction equation is as follows: M.sub.2+xImZ+2CO.sub.2==CO+M.sub.2CO.sub.3(ImZ) x, (x=1,2,3)

[0060] In one or more embodiments of the present application, M.sub.1 is first complexed with ImZ to form a free radical, has the ability to absorb and activate carbon dioxide, and reacts with M 2 and ImZ to form CO and M.sub.2CO.sub.3(ImZ) x. In this application, M.sub.1 and xImZ have the effect of catalytic activation after complexation, and a small amount is sufficient. Therefore, M1 (metal 1) plays an auxiliary catalytic role, and is always recycled and will not be consumed. ImZ not only plays a catalytic role but also participates in the reaction, M.sub.2 is a reactant, and finally combines with ImZ to generate carbonate.