CN1413908A - Method for synthetic ammonia - Google Patents
Method for synthetic ammonia Download PDFInfo
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- CN1413908A CN1413908A CN 02156731 CN02156731A CN1413908A CN 1413908 A CN1413908 A CN 1413908A CN 02156731 CN02156731 CN 02156731 CN 02156731 A CN02156731 A CN 02156731A CN 1413908 A CN1413908 A CN 1413908A
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- rare earth
- hydrogen
- synthetic ammonia
- ammonia
- nitrogen
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Abstract
A process for synthesizing ammonia includes such steps as heating the RE metal (or alloy) powder or block to the temp higher than the hydrogenation temp in the atmosphere preventing oxidizing and nitriding, introducing hydrogen gas to make the RE metal (or alloy) absorb hydrogen, introducing the mixture of oxygen and nitrogen gases or air, and chemical reaction. Its advantages are simple process and saving energy.
Description
Technical field:
The invention belongs to the preparing technical field of ammonia.
Background technology:
20 beginning of the century Harber and Mittasch etc. have developed the iron catalyst of synthetic ammonia, lay a good foundation for the industrialization of ammonia is synthetic.At present preparation of industrialization ammonia is to make hydrogen and nitrogen at 100-600 normal atmosphere under catalyst action, realizes under 400-600 ℃ of condition.In order further to reduce temperature of reaction and pressure, countries in the world never stop the research and development to synthetic ammonia catalyst for a long time.Discoveries such as Aika in 1972 are that the ruthenium catalyst of carrier has higher activity to synthetic ammonia with the gac, and Britain BP company starts to develop industrialization and has highly active ruthenium catalyst after the eighties in 20th century.But at present catalyst for reaction takes place in countries in the world send as an envoy to hydrogen and the nitrogen of exploitation of all failing under lesser temps and pressure, can't realize that more normal temperature and pressure is synthetic, and therefore the operation of reaction is many, the equipment complexity, and energy consumption is higher.
As everyone knows, hydrogen and nitrogen can become active hydrogen and nitrogen under the condition of discharge.Have the scholar to utilize this theory, (under 260～2600Pa) conditions, synthesized ammonia with nitrogen, hydrogen stream by microwave or radio frequency discharge, but this method equipment bulky complex, and synthetic efficient is very low, energy consumption is also very high at subatmospheric.At present, under the absence of discharge condition, synthetic ammonia does not appear in the newspapers as yet under normal temperature and pressure or lesser temps and the pressure.
Present industrial synthetic ammonia generally adopts following prepared in reaction:
Summary of the invention:
The novel method that the purpose of this invention is to provide a kind of synthetic ammonia, the raw material that adopts is hydrogen, oxygen and nitrogen, and metal or rare earth alloy are intermediate medium, behind intermediate medium absorption hydrogen, generate active nitrogen and hydrogen with oxygen and nitrogen effect again, finally synthetic ammonia.This method can be carried out at normal temperatures and pressures, improves productive rate and resultant velocity that temperature and pressure can improve ammonia, and the needed operation of this method is few, and equipment is simple, and can save a large amount of energy.
The present invention prepares the method for ammonia, and step is as follows:
(1) in the reaction atmosphere of anti-oxidation and nitrogenize, the rare earth metal or the rare earth alloy of block or powder is heated to more than the hydrogenation temperature;
(2) in reactor, feed hydrogen, make rare earth metal or rare earth alloy absorb hydrogen;
(3) mixed gas of aerating oxygen and nitrogen or air in reactor, rare earth metal or rare earth alloy hydrogenated products and oxygen and nitrogen generation chemical reaction are prepared ammonia.
According to the difference of rare earth metal or rare earth alloy, this speed of response and productive rate are different.The ammonia of preparing can be collected by methods such as air pump or flowing gas.After the reaction, can realize the regeneration of rare earth or rare earth alloy by reduction method.
In the described method, type of heating can be a resistive heating in the step (), LASER HEATING, plasma heating, electron beam heating or induction heating etc.Heat-processed can be carried out in the inert atmosphere of vacuum or non-nitrogen or reducing atmosphere, if adopt hydrogen, then can omit step (two).
In the described method, step (two) can be carried out simultaneously with step (one), promptly can feed hydrogen in heat-processed in reactor, also can stop the heating after carry out.
In the described method, the amount that feeds hydrogen in the step (two) gets final product can take place to inhale H-H reaction, and rare earth metal or rare earth alloy absorb the amount of hydrogen and be advisable to reach capacity.Hydrogen pressure improves, and the productive rate and the resultant velocity of ammonia improve thereupon.
In the described method, in the step (three), rare earth metal or rare earth alloy can be taken out the mixed gas that the residual hydrogen in mountain feeds nitrogen and oxygen again after absorbing hydrogen.Oxygen and nitrogen ratios can be according to adopting how much deciding of rare earth metal or rare earth alloy hydrogen.The amount that feeds nitrogen and oxygen mixture or air gets final product so that ammonia synthesis reaction can take place, and gaseous tension improves, and the productive rate and the resultant velocity of ammonia improve thereupon.
The productive rate of the transformation efficiency of ammonia and ammonia is relevant with employing rare earth metal or rare earth alloy system among the present invention, and can add reaction cocatalyst and promotor, improves the productive rate and the resultant velocity of ammonia.
Advantage of the present invention and positively effect: it is intermediate medium (or medium) that the present invention has adopted rare earth metal or rare earth alloy, and these intermediate mediums are being heated to hydrogenation temperature when above, can form micro mist after inhaling hydrogen; When being heated to the intermediate medium evaporation, can form nanometer superfine powder.The synthesis mechanism of ammonia is among the present invention, at first, by absorption of hydrogen protium is stored in rare earth metal or rare earth alloy micron order or the nanometer grade powder, and become the active hydrogen of ion or atomic condition by the hydrogen of gaseous phase, make the gas mixture generation chemisorption of micron order or nanometer grade powder and oxygen and nitrogen then, oxygen and nitrogen are in the surperficial activation of dissociating of metal hydride; Subsequently, surface chemical reaction at first takes place in metal hydride and oxygen, emits active hydrogen; At last, issued biochemical reaction generation ammonia by the nitrogen of metal hydride adsorption activation and active hydrogen at normal temperature and pressure or lower temperature and pressure.For the situation that adopts nano-scale particle, because its specific surface area is big, the surface shortcoming is many, and activity is very strong, and is stronger than micron-sized powder to the adsorptive power of gas, so its activation of dissociating is good, can improve the speed of response and the productive rate of synthetic ammonia.
Method of the present invention can be carried out at normal temperatures and pressures, improves productive rate and resultant velocity that temperature and pressure can improve ammonia, and needed operation is few, and equipment is simple, and can save a large amount of energy.
Embodiment:
Embodiment 1:
Adopt rare earth samarium preparation samarium hydride micron-sized powder earlier, the step of resynthesis ammonia is as follows:
(1) the rare earth metal samarium is put in the sample crucible of plasma furnace, under Ar (an about normal atmosphere) atmospheric condition, samarium metal is melted fully.
(2) stop heating, after vacuumizing, feed hydrogen in process furnace, samarium metal absorbs hydrogen and reaches capacity in the refrigerative process, forms the hydride of samarium, and is crushed into micron-sized powder.
(3) extract residual gas, bubbling air in process furnace out.
(4) samarium hydride micron particle and airborne oxygen and nitrogen generation chemical reaction are finally prepared ammonia.And adopt the Nessler's reagent check, what prove generation is ammonia.
Embodiment 2:
Adopt rare earth cerium preparation cerium hydride nano-particle earlier, the step of resynthesis ammonia is as follows:
(1) rare earth metal cerium is put in the sample crucible of plasma furnace, at 10%H
2Under+90%Ar (an about normal atmosphere altogether) atmospheric condition, making the metallic cerium evaporation and cooling off fast becomes nano particle.
(2) stop heating, the metallic cerium nano particle reacts with hydrogen in the refrigerative process, forms the hydride of cerium.
(3) after the cooling, extract residual gas out, bubbling air in process furnace.
(4) cerium hydride nano-particle and airborne oxygen and nitrogen generation chemical reaction are finally prepared ammonia.
And adopt the Nessler's reagent check, what prove generation is ammonia.
Embodiment 3:
Add auxiliary synthetic ammonia popular response catalyst Fe and promotor K
2O and Al
2O
3, adopting rare earth neodymium preparation neodymium hydride nano-particle earlier, the step of resynthesis ammonia is as follows:
(1) with synthetic ammonia popular response catalyst Fe and promotor K
2O and Al
2O
3Be dispersed in around the plasma furnace sample crucible, rare earth metal neodymium be put in the sample crucible of plasma furnace, at 10%H
2Under+90%Ar (an about normal atmosphere altogether) atmospheric condition, making the neodymium metal evaporation and cooling off fast becomes nano particle, and these nanoparticle deposition are to Fe, K
2O and Al
2O
3The surface.
(2) stop heating, the neodymium metal nano particle reacts with hydrogen in the refrigerative process, forms the hydride of neodymium.
(5) after the cooling, extract residual gas out, bubbling air in process furnace.
(6) neodymium hydride nano-particle and airborne oxygen and nitrogen generation chemical reaction are finally prepared ammonia.The synthetic ammonia is fed hydrochloric acid, and the concentration of check ammonia found that ammonia concentration slightly improves than no cocatalyst and promotor condition.
Claims (10)
1. the method for a synthetic ammonia, step is as follows:
(1) in the reaction atmosphere of anti-oxidation and nitrogenize, the rare earth metal or the rare earth alloy of block or powder is heated to more than the hydrogenation temperature;
(2) in reactor, feed hydrogen, make rare earth metal or rare earth alloy absorb hydrogen;
(3) mixed gas of aerating oxygen and nitrogen or air in reactor, rare earth metal or rare earth alloy hydrogenated products and oxygen and nitrogen generation chemical reaction are prepared ammonia.
2. the method for synthetic ammonia as claimed in claim 1 is characterized in that type of heating is a resistive heating in the step (), LASER HEATING, plasma heating, electron beam heating or induction heating.
3. the method for synthetic ammonia as claimed in claim 1 is characterized in that the reaction atmosphere described in the step () is the inert atmosphere or the reducing atmosphere of vacuum or non-nitrogen.
4. as the method for claim 1 or 2 or 3 described synthetic ammonia, it is characterized in that step (two) and step () carry out simultaneously, promptly in heat-processed, in reactor, feed hydrogen.
5. as the method for claim 1 or 2 or 3 described synthetic ammonia, it is characterized in that the amount of step (two) middle-weight rare earths metal or rare earth alloy absorption hydrogen is as the criterion to reach capacity.
6. the method for synthetic ammonia as claimed in claim 4 is characterized in that the amount of step (two) middle-weight rare earths metal or rare earth alloy absorption hydrogen is as the criterion to reach capacity.
7. as the method for claim 1 or 2 or 3 described synthetic ammonia, it is characterized in that step (three) middle-weight rare earths metal or rare earth alloy absorb hydrogen after, extract mixed gas or the air that residual hydrogen feeds nitrogen and oxygen more earlier out.
8. the method for synthetic ammonia as claimed in claim 4, it is characterized in that step (three) middle-weight rare earths metal or rare earth alloy absorb hydrogen after, extract mixed gas or the air that residual hydrogen feeds nitrogen and oxygen more earlier out.
9. the method for synthetic ammonia as claimed in claim 5, it is characterized in that step (three) middle-weight rare earths metal or rare earth alloy absorb hydrogen and reach capacity after, extract mixed gas or the air that residual hydrogen feeds nitrogen and oxygen more earlier out.
10. the method for synthetic ammonia as claimed in claim 1 is characterized in that adding in the synthesis step reaction cocatalyst and promotor.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB02156731XA CN1170771C (en) | 2002-12-18 | 2002-12-18 | Method for synthetic ammonia |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB02156731XA CN1170771C (en) | 2002-12-18 | 2002-12-18 | Method for synthetic ammonia |
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| Publication Number | Publication Date |
|---|---|
| CN1413908A true CN1413908A (en) | 2003-04-30 |
| CN1170771C CN1170771C (en) | 2004-10-13 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB02156731XA Expired - Fee Related CN1170771C (en) | 2002-12-18 | 2002-12-18 | Method for synthetic ammonia |
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Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI427035B (en) * | 2011-08-02 | 2014-02-21 | Univ Nat Pingtung Sci & Tech | A device for producing ammonia |
| CN106276972A (en) * | 2016-08-25 | 2017-01-04 | 昆明理工大学 | A kind of method utilizing nitrogen and hydration ammonification |
| CN108348902A (en) * | 2015-11-10 | 2018-07-31 | 国立研究开发法人科学技术振兴机构 | Metal load content, metal supported catalyst and the ammonia synthesis using the catalyst |
| CN109803923A (en) * | 2016-10-19 | 2019-05-24 | 国立研究开发法人物质·材料研究机构 | Synthesize the method and device thereof of ammonia |
| CN109833910A (en) * | 2017-11-28 | 2019-06-04 | 中国科学院大连化学物理研究所 | A kind of catalyst for ammonia synthesis reaction |
| CN110831899A (en) * | 2017-07-03 | 2020-02-21 | 维多利亚联科有限公司 | Ammonia production method and apparatus for ammonia production |
| CN111163862A (en) * | 2017-05-26 | 2020-05-15 | 星火能源 | From NH3Removal of gaseous NH from a reactor product stream3 |
| CN112250088A (en) * | 2020-10-30 | 2021-01-22 | 上海科技大学 | Method for catalytically synthesizing ammonia based on liquid alloy |
| CN112645353A (en) * | 2021-01-27 | 2021-04-13 | 复旦大学 | Method for enhancing selectivity of synthetic ammonia by ball milling nitrogen-hydrogen mixed gas under normal temperature and pressure water phase |
| CN112875723A (en) * | 2021-01-27 | 2021-06-01 | 复旦大学 | Method for synthesizing ammonia under water phase condition at normal temperature and pressure |
| WO2022089658A1 (en) * | 2020-10-30 | 2022-05-05 | 上海科技大学 | Method for catalytically synthesizing ammonia at atmospheric pressure |
| CN115536041A (en) * | 2022-08-31 | 2022-12-30 | 中山大学 | Method for activating and curing nitrogen by laser |
| CN115744933A (en) * | 2022-11-10 | 2023-03-07 | 中国华能集团清洁能源技术研究院有限公司 | Green ammonia production system and method |
-
2002
- 2002-12-18 CN CNB02156731XA patent/CN1170771C/en not_active Expired - Fee Related
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI427035B (en) * | 2011-08-02 | 2014-02-21 | Univ Nat Pingtung Sci & Tech | A device for producing ammonia |
| US10759668B2 (en) | 2015-11-10 | 2020-09-01 | Japan Science And Technology Agency | Supported metal material, supported metal catalyst, and ammonia synthesis method using the same |
| CN108348902A (en) * | 2015-11-10 | 2018-07-31 | 国立研究开发法人科学技术振兴机构 | Metal load content, metal supported catalyst and the ammonia synthesis using the catalyst |
| CN108348902B (en) * | 2015-11-10 | 2021-02-09 | 国立研究开发法人科学技术振兴机构 | Metal carrier, metal-carrying catalyst, and ammonia synthesis method using the catalyst |
| CN106276972A (en) * | 2016-08-25 | 2017-01-04 | 昆明理工大学 | A kind of method utilizing nitrogen and hydration ammonification |
| CN109803923A (en) * | 2016-10-19 | 2019-05-24 | 国立研究开发法人物质·材料研究机构 | Synthesize the method and device thereof of ammonia |
| CN111163862A (en) * | 2017-05-26 | 2020-05-15 | 星火能源 | From NH3Removal of gaseous NH from a reactor product stream3 |
| CN110831899A (en) * | 2017-07-03 | 2020-02-21 | 维多利亚联科有限公司 | Ammonia production method and apparatus for ammonia production |
| CN110831899B (en) * | 2017-07-03 | 2023-05-26 | 维多利亚联科有限公司 | Ammonia production method and device for ammonia production |
| CN109833910A (en) * | 2017-11-28 | 2019-06-04 | 中国科学院大连化学物理研究所 | A kind of catalyst for ammonia synthesis reaction |
| CN109833910B (en) * | 2017-11-28 | 2022-05-31 | 中国科学院大连化学物理研究所 | Catalyst for synthetic ammonia reaction |
| CN112250088A (en) * | 2020-10-30 | 2021-01-22 | 上海科技大学 | Method for catalytically synthesizing ammonia based on liquid alloy |
| CN112250088B (en) * | 2020-10-30 | 2022-04-01 | 上海科技大学 | Method for catalytically synthesizing ammonia based on liquid alloy |
| WO2022089658A1 (en) * | 2020-10-30 | 2022-05-05 | 上海科技大学 | Method for catalytically synthesizing ammonia at atmospheric pressure |
| CN112645353A (en) * | 2021-01-27 | 2021-04-13 | 复旦大学 | Method for enhancing selectivity of synthetic ammonia by ball milling nitrogen-hydrogen mixed gas under normal temperature and pressure water phase |
| CN112875723B (en) * | 2021-01-27 | 2022-05-20 | 复旦大学 | Method for synthesizing ammonia under normal temperature and pressure water phase condition |
| CN112645353B (en) * | 2021-01-27 | 2022-05-20 | 复旦大学 | Method for enhancing selectivity of synthetic ammonia by ball milling nitrogen-hydrogen mixed gas under normal temperature and normal pressure water phase |
| CN112875723A (en) * | 2021-01-27 | 2021-06-01 | 复旦大学 | Method for synthesizing ammonia under water phase condition at normal temperature and pressure |
| CN115536041A (en) * | 2022-08-31 | 2022-12-30 | 中山大学 | Method for activating and curing nitrogen by laser |
| CN115536041B (en) * | 2022-08-31 | 2024-05-28 | 中山大学 | Method for activating and solidifying nitrogen by laser |
| CN115744933A (en) * | 2022-11-10 | 2023-03-07 | 中国华能集团清洁能源技术研究院有限公司 | Green ammonia production system and method |
| CN115744933B (en) * | 2022-11-10 | 2024-02-06 | 中国华能集团清洁能源技术研究院有限公司 | Green ammonia production system and method |
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| Publication number | Publication date |
|---|---|
| CN1170771C (en) | 2004-10-13 |
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