CN114314793A - Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof - Google Patents
Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof Download PDFInfo
- Publication number
- CN114314793A CN114314793A CN202210010213.7A CN202210010213A CN114314793A CN 114314793 A CN114314793 A CN 114314793A CN 202210010213 A CN202210010213 A CN 202210010213A CN 114314793 A CN114314793 A CN 114314793A
- Authority
- CN
- China
- Prior art keywords
- hydrogen
- producing
- powder
- water
- hydrogen production
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 128
- 239000001257 hydrogen Substances 0.000 title claims abstract description 128
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 128
- 239000002245 particle Substances 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 46
- 239000000463 material Substances 0.000 claims abstract description 32
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 13
- 230000035622 drinking Effects 0.000 claims abstract description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 14
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims description 14
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 claims description 11
- 238000001354 calcination Methods 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 8
- 239000005995 Aluminium silicate Substances 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- 229910021536 Zeolite Inorganic materials 0.000 claims description 7
- 235000012211 aluminium silicate Nutrition 0.000 claims description 7
- 239000000440 bentonite Substances 0.000 claims description 7
- 229910000278 bentonite Inorganic materials 0.000 claims description 7
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 7
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 7
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 7
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 7
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 7
- 229960003080 taurine Drugs 0.000 claims description 7
- 239000010457 zeolite Substances 0.000 claims description 7
- 238000000498 ball milling Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- 230000003578 releasing effect Effects 0.000 claims description 6
- 238000012216 screening Methods 0.000 claims description 6
- 239000004575 stone Substances 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 229910012375 magnesium hydride Inorganic materials 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 229910045601 alloy Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000011812 mixed powder Substances 0.000 claims description 3
- 238000009920 food preservation Methods 0.000 claims description 2
- 229910052613 tourmaline Inorganic materials 0.000 claims description 2
- 229940070527 tourmaline Drugs 0.000 claims description 2
- 239000011032 tourmaline Substances 0.000 claims description 2
- 238000004080 punching Methods 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 238000009776 industrial production Methods 0.000 abstract 1
- 230000009286 beneficial effect Effects 0.000 description 4
- 230000009982 effect on human Effects 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 241000237858 Gastropoda Species 0.000 description 3
- 150000004678 hydrides Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000002366 mineral element Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000011573 trace mineral Substances 0.000 description 2
- 235000013619 trace mineral Nutrition 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000190070 Sarracenia purpurea Species 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The invention belongs to the technical field of hydrogen production, and particularly relates to hydrogen production particles capable of generating a porous structure on site. The hydrogen production particles comprise: hydrogen release material and auxiliary agent. The invention also discloses a preparation method and application of the hydrogen production particles. The preparation process of the hydrogen production particles is simple and is very suitable for industrial production. The hydrogen production particles can quickly release hydrogen when meeting water, are suitable for a plurality of application scenes, and particularly meet the requirement of modern people on daily health care by drinking hydrogen-rich water.
Description
Technical Field
The invention belongs to the technical field of hydrogen production, and particularly relates to hydrogen production particles capable of generating a porous structure on site, and a preparation method and application thereof.
Background
Hydrogen has no toxic hazard and side effect on human body, is praised as the most effective and most ideal antioxidant and is widely applied. In recent years, a plurality of scholars research the biological effect of hydrogen and find that the hydrogen has an important health-care effect on human bodies. After entering human body, the hydrogen can permeate into the whole body rapidly, penetrate cell membrane, take away malignant active oxygen, and synthesize water to be discharged out of the body. At the same time, hydrogen also restores the cells that have been destroyed and oxidized.
Hydrogen-rich water, as the name implies, refers to water that contains abundant molecular hydrogen. The hydrogen-rich water is different from common water in that it has reducing power, can eliminate excess active oxygen in human body, purify blood, promote metabolism, prevent various diseases and is beneficial to human health. Currently, there are probably three following methods for the preparation of hydrogen-rich water: the first method is that hydrogen is directly dissolved in water through high-pressure equipment to form saturated hydrogen-rich water, but the cost of the high-pressure equipment is high, and the storage stability of the prepared hydrogen-rich water is poor; the second method is to dissolve hydrogen generated by electrolyzing water into water by an electrochemical method, but the type of products sold in the market at present are mixed, and simultaneously, the prepared hydrogen-rich water has lower concentration. The third is to put the hydrogen-producing particles into water and prepare hydrogen-rich water by utilizing a micro-electrolysis technology, however, the existing hydrogen-producing particles in the market cannot release hydrogen rapidly in order to ensure that the hydrogen-releasing effect is stable for a long time, so that the concentration of the hydrogen-rich water is difficult to improve and the health-care effect on human bodies is exerted.
Therefore, hydrogen production particles which can be conveniently and safely used and can rapidly release hydrogen are expected. When the hydrogen production particles are placed in a sealed water cup with a certain volume, not only can super-saturated hydrogen-rich water be obtained in a short time, but also natural mineral elements can be enriched in the water, and the health care effect on human bodies is exerted.
The present invention has been made to solve the above problems.
Disclosure of Invention
Aiming at the defects of the prior art, the invention provides hydrogen production particles capable of generating a porous structure on site.
The invention provides a hydrogen production particle capable of producing a porous structure on site, which comprises the following raw materials in parts by weight: 10-50 parts of hydrogen release material and 50-90 parts of auxiliary agent.
The hydrogen evolution material comprises a first hydrogen evolution material and a second hydrogen evolution material.
The first hydrogen evolution material comprises metallic magnesium powder, iron powder, zinc powder, aluminum powder or alloy powder comprising at least one of the foregoing.
The second hydrogen evolution material comprises calcium hydride or magnesium hydride.
The auxiliary agent comprises one or more of kaolin, bentonite, medical stone, zeolite, silicon oxide, cerium oxide and taurine.
The grain diameter of each component needs to be less than 50 mu m.
Preferably, the hydrogen release material comprises the following raw materials in percentage by weight:
the first hydrogen evolution material is 90-99.9 percent, and the second hydrogen evolution material is 0.1-10 percent.
The first hydrogen evolution material can be selected from magnesium powder, iron powder, zinc powder, aluminum powder or alloy powder containing at least one of the above materials.
The second hydrogen evolution material comprises calcium hydride or magnesium hydride.
The auxiliary agent comprises the following raw materials in percentage by weight:
50-70% of kaolin, 5-15% of bentonite, 5-15% of tourmaline, 5-15% of zeolite, 5-15% of silicon oxide, 0.1-5% of cerium oxide and 1-10% of taurine.
Wherein, the kaolin can be used as a main component of the sintered ceramic; the bentonite can be used as a binder; the medical stone contains various mineral elements beneficial to the growth and development of a human body, can be dissolved out of various trace elements and rare earth elements after being soaked in water, and has good adsorption effect; the zeolite has natural micropore structure, and can increase the specific surface area of the hydrogen producing particles, so that the hydrogen producing particles have more micropore structures. The addition of the silicon oxide can reduce the sintering temperature of the hydrogen production particles, and save more energy; cerium oxide has excellent antibacterial properties; taurine is not easily decomposed at high temperature, and appropriate acidity helps to neutralize alkaline substances generated after hydride hydrolyzes and releases hydrogen.
The second aspect of the present invention provides a method for producing the hydrogen-producing particles, comprising:
(1) ball milling and mixing
Ball-milling the hydrogen release material and the auxiliary agent for 2-5h respectively until the particle size of the powder is less than 50 μm, pouring the ball-milled hydrogen release material and auxiliary agent into a mixing pot, and mixing for 15-30min to ensure that the components are uniformly mixed.
(2) Punch forming
And (2) pouring the mixed powder obtained in the step (1) into a punch press for punch forming.
(3) Calcination screening
And (3) calcining the product formed in the step (2) in a 200-500 ℃ tube furnace under an inert atmosphere for 0.5-5h, and screening to obtain the hydrogen production particles.
Preferably, the calcination temperature is 300 ℃ and the calcination time is 1 h.
Preferably, the hydrogen-producing particles may be spherical, flaky, or columnar.
Such as nitrogen, argon, and the like.
After being prepared, the hydrogen production particles can be wrapped in a breathable and water-permeable packaging bag, then are sterilized by ultraviolet rays and are stored in a dry, cool and ventilated place.
A third aspect of the invention relates to the use of the hydrogen-producing particles of the first aspect for the preparation of hydrogen-enriched water for drinking or for contact with water in the food preservation, cultivation and growing industries for the production of hydrogen.
The invention has the following beneficial effects:
(1) compared with the traditional hydrogen production particles only added with metal powder, the hydrogen production particles of the invention are also added with a certain amount of hydride, such as calcium hydride or magnesium hydride, and can be rapidly decomposed in water to release hydrogen, and simultaneously, a porous ceramic structure can be further formed on site, so that the contact area between the hydrogen production particles and water is greatly increased, the metal powder is further promoted to form a galvanic cell effect, the metal powder in the hydrogen production particles reacts more thoroughly, and the hydrogen evolution speed of the hydrogen production particles is greatly improved. For example, 1 part of hydrogen-producing particles is added to 100 parts of water in a mass ratio and placed in a sealed container, and after 15 minutes, the hydrogen molecule content in the hydrogen-rich water can reach up to 800 ppb.
(2) The hydrogen production particles are added with natural minerals to ensure that the hydrogen-rich water is rich in trace elements such as magnesium, zinc, calcium and the like while decomposing and releasing hydrogen, thus being beneficial to improving the drinking water quality of human bodies and playing the health care role on the human bodies.
Drawings
FIG. 1 is a graph showing the change in hydrogen concentration in the hydrogen-rich water according to example 1 with time.
Fig. 2 is a graph showing the change in hydrogen concentration in the hydrogen-rich water with time in example 2.
Fig. 3 is a graph showing the change in hydrogen concentration in the hydrogen-rich water of comparative example 1 with time.
Detailed Description
The present invention will be further described with reference to the following embodiments.
Example 1
(1) Ball milling and mixing
Preparing 2g of magnesium powder and 1g of calcium hydride as hydrogen release materials; 5g of kaolin, 1g of bentonite, 1g of medical stone, 1g of zeolite, 0.5g of silicon oxide, 0.05g of cerium oxide and 0.5g of taurine are prepared as auxiliaries.
Grinding auxiliary agents such as kaolin, bentonite, medical stone, zeolite, silicon oxide, cerium oxide and taurine for 2-5h until the particle size of the powder is smaller than 50 mu m, simultaneously ball-grinding the hydrogen release material for 2-5h until the particle size of the powder is smaller than 50 mu m, pouring the ball-ground hydrogen release material and the auxiliary agents into a mixing pot, and mixing for 15-30min to ensure that all the components are uniformly mixed.
(2) Punch forming
And (2) pouring the mixed powder obtained in the step (1) into a punch press for punch forming.
(3) Calcination screening
And (3) calcining the product formed in the step (2) in a tubular furnace at 300 ℃ for 1 hour, and screening to obtain the hydrogen production particles.
Specific data: in a closed container, 2g of hydrogen production particles are placed in 200ml of water, and the concentration of hydrogen in the prepared water is detected by a snail hydrogen pen, as shown in figure 1, the concentration of hydrogen in the solution can reach 800ppb after 15 min.
Example 2
The difference from example 1 was only that 2g of magnesium powder, 0.5g of calcium hydride as a hydrogen-releasing material were prepared in step (1).
Specific data: in a closed container, 2g of hydrogen production particles are placed in 200ml of water, and the concentration of hydrogen in the prepared water is detected by a snail hydrogen pen, as shown in fig. 2, the concentration of hydrogen in the solution can reach 600ppb after 15 min. Compared with the embodiment 1, the hydrogen concentration is reduced because the adding amount of calcium hydride is reduced by half, so that the porous structure generated on site by hydrogen production particles is not enough, a part of magnesium powder is not fully contacted and reacted with water. Meanwhile, calcium hydride reacts with water rapidly, releases hydrogen rapidly in a short time and is discharged from water, and the released hydrogen has low solubility in water. The amount of calcium hydride is therefore reduced, resulting in a reduction in the amount of hydrogen produced by its reaction with water, resulting in a reduction in the hydrogen concentration in the final aqueous solution, which is a negligible factor.
Comparative example 1
The difference from example 1 is that in step (1), 2g of magnesium powder was prepared as a hydrogen-releasing material without adding calcium hydride or other hydride.
Specific data: in a closed container, 2g of hydrogen production particles are placed in 200ml of water, and the concentration of hydrogen in the prepared water is detected by a snail hydrogen pen, as shown in fig. 3, the concentration of hydrogen in the solution can only reach 100ppb after 30 min. It can be seen that if calcium hydride is not added, most of the magnesium powder can not directly contact with water and completely react due to the fact that a porous structure cannot be generated in situ in the contact process of the magnesium powder and the water, the released hydrogen amount is very low, and further the hydrogen concentration in the water is very low.
The above description is only for the specific embodiment of the present invention, but the scope of the present invention is not limited thereto, and any changes or substitutions that can be easily conceived by those skilled in the art within the technical scope of the present invention are included in the scope of the present invention.
Claims (8)
1. The hydrogen production particle capable of producing the porous structure on site is characterized by comprising the following raw materials in parts by weight: 10-50 parts of hydrogen release material and 50-90 parts of auxiliary agent;
wherein the hydrogen evolution material comprises a first hydrogen evolution material and a second hydrogen evolution material;
the first hydrogen evolution material comprises metal magnesium powder, iron powder, zinc powder, aluminum powder or alloy powder comprising at least one of the foregoing;
the second hydrogen evolution material comprises calcium hydride or magnesium hydride;
the auxiliary agent comprises one or more of kaolin, bentonite, medical stone, zeolite, silicon oxide, cerium oxide and taurine.
2. The hydrogen-producing particle of claim 1, wherein the hydrogen-releasing material is made from the following raw materials in weight percent: the first hydrogen evolution material is 90-99.9 percent, and the second hydrogen evolution material is 0.1-10 percent.
3. The hydrogen-producing particle of claim 1, wherein the additive is prepared from the following raw materials in weight percent: 50-70% of kaolin, 5-15% of bentonite, 5-15% of tourmaline, 5-15% of zeolite, 5-15% of silicon oxide, 0.1-5% of cerium oxide and 1-10% of taurine.
4. The hydrogen-producing particle of claim 1, wherein the hydrogen-producing particle is in the form of a sheet, sphere, or cylinder.
5. The method of producing hydrogen-producing particles according to claim 1, comprising the steps of:
(1) ball milling and mixing
Ball-milling the hydrogen release material and the auxiliary agent for 2-5h respectively, and pouring the ball-milled hydrogen release material and auxiliary agent into a mixing pot to mix for 15-30min to ensure that all components are uniformly mixed;
(2) punch forming
Pouring the mixed powder obtained in the step (1) into a punching machine for punching and forming;
(3) calcination screening
And (3) calcining the product formed in the step (2) in a 200-500 ℃ tube furnace under an inert atmosphere for 0.5-5h, and screening to obtain the hydrogen production particles.
6. The method for producing hydrogen-producing particles according to claim 5, wherein the calcination temperature is 300 ℃ and the calcination time is 1 hour.
7. The method for preparing hydrogen-producing particles according to claim 5, wherein the particle size of the obtained powder is less than 50 μm after ball milling of the hydrogen-releasing material and the auxiliary agent for 2-5 h.
8. Use of the hydrogen-producing particles of claim 1 for the production of hydrogen-rich water for drinking or for contact with water in the food preservation, cultivation and growing industries to produce hydrogen.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210010213.7A CN114314793A (en) | 2022-01-06 | 2022-01-06 | Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210010213.7A CN114314793A (en) | 2022-01-06 | 2022-01-06 | Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN114314793A true CN114314793A (en) | 2022-04-12 |
Family
ID=81024847
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210010213.7A Pending CN114314793A (en) | 2022-01-06 | 2022-01-06 | Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114314793A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115812702A (en) * | 2022-12-30 | 2023-03-21 | 深圳市芭田生态工程股份有限公司 | Controllable hydrogen release capsule and preparation method and application thereof |
CN116022733A (en) * | 2023-02-24 | 2023-04-28 | 四川卡文智氢新能源有限公司 | Control method for aluminium hydrolysis hydrogen production process |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH438234A (en) * | 1963-07-30 | 1967-06-30 | Basf Ag | Process for the production of hydrogen |
JP2008037683A (en) * | 2006-08-03 | 2008-02-21 | Aquafairy Kk | Hydrogen-generating agent, and apparatus and method for generating hydrogen |
CN104016470A (en) * | 2013-03-01 | 2014-09-03 | 百泉利康 | Method and apparatus to produce hydrogen-rich materials |
JP5740659B1 (en) * | 2014-11-07 | 2015-06-24 | 有限会社プレジール | Hydrogen aqueous solution, hydrogen aqueous solution manufacturing kit, and hydrogen aqueous solution manufacturing method |
CN105084468A (en) * | 2015-07-30 | 2015-11-25 | 济南木齐健康科技有限公司 | Ceramal material for manufacturing hydrogen-enriched water and preparing method and application thereof |
CN106629594A (en) * | 2016-11-15 | 2017-05-10 | 青岛大学 | High-performance magnesium hydride invertible hydrogen manufacturing system and hydrogen manufacturing method |
CN107573047A (en) * | 2017-08-22 | 2018-01-12 | 深圳市和之科技有限公司 | Hydrogen manufacturing ceramic water material and its preparation method and application |
CN108727007A (en) * | 2018-07-20 | 2018-11-02 | 天津嘉宝艾依琳科技发展有限公司 | More effect water purification ceramic materials and its preparation method and application |
CN109250683A (en) * | 2018-09-30 | 2019-01-22 | 武汉市能智达科技有限公司 | It is a kind of using magnesium hydride as the hydrogen production process of hydrogen storage material and device |
JP2019182699A (en) * | 2018-04-06 | 2019-10-24 | 東洋アルミニウム株式会社 | Hydrogen generating material and manufacturing method therefor |
CN110980636A (en) * | 2019-12-31 | 2020-04-10 | 世能氢电科技有限公司 | Magnesium hydride hydrogen storage composite material containing porous material and preparation method thereof |
-
2022
- 2022-01-06 CN CN202210010213.7A patent/CN114314793A/en active Pending
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH438234A (en) * | 1963-07-30 | 1967-06-30 | Basf Ag | Process for the production of hydrogen |
JP2008037683A (en) * | 2006-08-03 | 2008-02-21 | Aquafairy Kk | Hydrogen-generating agent, and apparatus and method for generating hydrogen |
CN104016470A (en) * | 2013-03-01 | 2014-09-03 | 百泉利康 | Method and apparatus to produce hydrogen-rich materials |
JP5740659B1 (en) * | 2014-11-07 | 2015-06-24 | 有限会社プレジール | Hydrogen aqueous solution, hydrogen aqueous solution manufacturing kit, and hydrogen aqueous solution manufacturing method |
CN105084468A (en) * | 2015-07-30 | 2015-11-25 | 济南木齐健康科技有限公司 | Ceramal material for manufacturing hydrogen-enriched water and preparing method and application thereof |
CN106629594A (en) * | 2016-11-15 | 2017-05-10 | 青岛大学 | High-performance magnesium hydride invertible hydrogen manufacturing system and hydrogen manufacturing method |
CN107573047A (en) * | 2017-08-22 | 2018-01-12 | 深圳市和之科技有限公司 | Hydrogen manufacturing ceramic water material and its preparation method and application |
JP2019182699A (en) * | 2018-04-06 | 2019-10-24 | 東洋アルミニウム株式会社 | Hydrogen generating material and manufacturing method therefor |
CN108727007A (en) * | 2018-07-20 | 2018-11-02 | 天津嘉宝艾依琳科技发展有限公司 | More effect water purification ceramic materials and its preparation method and application |
CN109250683A (en) * | 2018-09-30 | 2019-01-22 | 武汉市能智达科技有限公司 | It is a kind of using magnesium hydride as the hydrogen production process of hydrogen storage material and device |
CN110980636A (en) * | 2019-12-31 | 2020-04-10 | 世能氢电科技有限公司 | Magnesium hydride hydrogen storage composite material containing porous material and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
李大鹏, 国防工业出版社 * |
黄旭: "Li-(Mg)-B-H储氢体系的动力学与热力学调控及其机理研究", 《中国博士学位论文全文数据库(电子期刊) 工程科技I辑》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115812702A (en) * | 2022-12-30 | 2023-03-21 | 深圳市芭田生态工程股份有限公司 | Controllable hydrogen release capsule and preparation method and application thereof |
CN116022733A (en) * | 2023-02-24 | 2023-04-28 | 四川卡文智氢新能源有限公司 | Control method for aluminium hydrolysis hydrogen production process |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN114314793A (en) | Hydrogen production particle capable of generating porous structure on site and preparation method and application thereof | |
CN108623224B (en) | Reduction antibacterial material and preparation method thereof | |
JP4233601B1 (en) | Method for producing rice cake powder | |
CN106115621B (en) | Graphene activates hydrogen manufacturing material and its preparation method and application | |
CN108727007A (en) | More effect water purification ceramic materials and its preparation method and application | |
CN101774672B (en) | Functional material for preparing multifunctional healthy running water and preparation method thereof | |
CN110743549B (en) | Preparation method of copper-based heterogeneous catalyst taking activated carbon spheres as carrier for wet oxidation | |
CN107597143A (en) | A kind of metal nanoparticle is uniformly embedded into the controllable method for preparing of the elctro-catalyst of mesoporous carbon spheres internal structure | |
CN113105221B (en) | Negative hydrogen ion water activating material and its producing method | |
CN114848513A (en) | Composite hydrogen-rich material and preparation method thereof | |
CN102432326A (en) | Porous carbon-titanium dioxide compound material and preparation method thereof | |
CN102500167B (en) | Core-shell structure composite filter material for water treatment and preparation method thereof | |
CN100512950C (en) | Manganese series deoxidants and their preparation process | |
Abdieva et al. | RETRACTED: An Efficient Ultrasound-Assisted Synthesis of Cu/Zn Hybrid MOF Nanostructures With High Microbial Strain Performance | |
CN110078192A (en) | A kind of mineral water and preparation method thereof | |
CN107349933B (en) | A kind of Industrial Wastewater Treatment active iron C catalyst | |
CN115779905B (en) | Iron oxide biochar with Taihu blue algae as raw material, preparation method thereof and application thereof in water treatment | |
CN109179620B (en) | Combined multifunctional health-preserving hydrogen-rich water sheet | |
WO2023051150A1 (en) | Rare earth auxiliary agent and preparation method therefor | |
CN105753503A (en) | Electrocatalysis particle electrode for efficiently degrading bisphenol A in wastewater and preparation method of electrocatalysis particle electrode | |
CN101613148B (en) | Method for removing nitrate nitrogen, corresponding combination preparation, and preparation method and application thereof | |
CN104307575A (en) | Base metal composite catalyst, preparation method and use thereof | |
CN111167403A (en) | Composite functional material for synchronously removing nitrogen and phosphorus and preparation method thereof | |
CN118619202A (en) | Hydrogen source supply material for hydrogen-rich water and preparation method thereof | |
CN115487792A (en) | Preparation method of magnetic activated carbon |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20220412 |