CN115710722A - Hydrolysis hydrogen production system and use method thereof - Google Patents
Hydrolysis hydrogen production system and use method thereof Download PDFInfo
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 239000001257 hydrogen Substances 0.000 title claims abstract description 68
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 68
- 238000006460 hydrolysis reaction Methods 0.000 title claims abstract description 46
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 46
- 230000007062 hydrolysis Effects 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims abstract description 68
- 239000000376 reactant Substances 0.000 claims abstract description 59
- 238000005338 heat storage Methods 0.000 claims abstract description 38
- 238000010248 power generation Methods 0.000 claims abstract description 29
- 230000017525 heat dissipation Effects 0.000 claims abstract description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 53
- 239000007864 aqueous solution Substances 0.000 claims description 29
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 229910052987 metal hydride Inorganic materials 0.000 claims description 17
- 150000004681 metal hydrides Chemical group 0.000 claims description 17
- 229910000577 Silicon-germanium Inorganic materials 0.000 claims description 16
- 239000007788 liquid Substances 0.000 claims description 15
- RSHAOIXHUHAZPM-UHFFFAOYSA-N magnesium hydride Chemical compound [MgH2] RSHAOIXHUHAZPM-UHFFFAOYSA-N 0.000 claims description 10
- 229910012375 magnesium hydride Inorganic materials 0.000 claims description 10
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 10
- 239000012279 sodium borohydride Substances 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 10
- 239000008188 pellet Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 230000005611 electricity Effects 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 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 4
- SIAPCJWMELPYOE-UHFFFAOYSA-N lithium hydride Chemical compound [LiH] SIAPCJWMELPYOE-UHFFFAOYSA-N 0.000 claims description 4
- 229910000103 lithium hydride Inorganic materials 0.000 claims description 4
- 229910000838 Al alloy Inorganic materials 0.000 claims description 3
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 239000004020 conductor Substances 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 3
- 229910001220 stainless steel Inorganic materials 0.000 claims description 3
- 230000007704 transition Effects 0.000 claims 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 238000001816 cooling Methods 0.000 abstract description 17
- 239000002918 waste heat Substances 0.000 abstract description 3
- 239000003570 air Substances 0.000 description 9
- 239000000446 fuel Substances 0.000 description 7
- 235000011187 glycerol Nutrition 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000012188 paraffin wax Substances 0.000 description 6
- 239000002699 waste material Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 239000002131 composite material Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910002899 Bi2Te3 Inorganic materials 0.000 description 2
- 230000004308 accommodation Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012080 ambient air Substances 0.000 description 1
- 208000012839 conversion disease Diseases 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000007726 management method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
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Abstract
本发明涉及一种水解制氢系统及其使用方法,涉及制氢技术领域,包括反应器、供料组件和发电组件。先将所述第一反应物和第二反应物分别通入所述反应空间内,所述相变储热层设于所述反应器的外侧壁以形成热端,所述散热翅片设于所述温差电池组的外侧且置于空气中以形成冷端,所述温差电池组经由所述热端和冷端的两端温度差进行温差发电,通过所述温差电池组可持续吸收反应产生的热量并利用,且能够使所述反应空间内的温度稳定,有利于持续稳定的制取氢气,设置所述相变储热层、温差电池组和散热翅片,一方面可通过热端持续吸收反应热并配合冷端进行发电,另一方面可通过所述散热翅片向空气中持续散除余热,有利于稳定的发电。
The invention relates to a hydrolysis hydrogen production system and its use method, and relates to the technical field of hydrogen production, including a reactor, a feed assembly and a power generation assembly. The first reactant and the second reactant are respectively passed into the reaction space, the phase change heat storage layer is arranged on the outer wall of the reactor to form a hot end, and the heat dissipation fin is arranged on The outside of the thermoelectric battery pack is placed in the air to form a cold end. The thermoelectric battery pack performs thermoelectric power generation through the temperature difference between the hot end and the cold end. The heat can be used in parallel, and the temperature in the reaction space can be stabilized, which is conducive to the continuous and stable production of hydrogen. The phase change heat storage layer, thermoelectric battery pack and cooling fins are set up, on the one hand, it can continuously absorb through the hot end The reaction heat is combined with the cold end to generate power. On the other hand, the waste heat can be continuously dissipated into the air through the heat dissipation fins, which is conducive to stable power generation.
Description
技术领域technical field
本发明涉及制氢技术领域,尤其涉及一种水解制氢系统及其使用方法。The invention relates to the technical field of hydrogen production, in particular to a hydrolysis hydrogen production system and its use method.
背景技术Background technique
燃料电池动力系统具有高能量转换效率、低排放、运行噪声小和适应不同功率要求等优势,是常规动力系统的重要选项。目前燃料电池动力系统主要应用方向为:船舶、车辆以及水下装备。随着燃料电池技术发展完善,燃料电池动力系统将得到广泛应用。目前长续航力是燃料电池动力系统发展的重大瓶颈。通过大幅提高氢源储氢密度,进而提升燃料电池动力系统能量密度,已经成为发展长续航力燃料电池动力系统的关键,然而目前主流的高压氢气瓶无法满足高能量密度的需求。以硼氢化钠、氢化镁、氢化钙和氢化锂为代表的金属氢化物通过水解制氢,储氢密度最高可达25wt%,是35MPa高压气瓶储氢密度的7倍以上,是最具先进性的氢源技术之一。The fuel cell power system has the advantages of high energy conversion efficiency, low emission, low operating noise and adaptability to different power requirements, and is an important option for conventional power systems. At present, the main application directions of fuel cell power systems are: ships, vehicles and underwater equipment. With the development and improvement of fuel cell technology, fuel cell power systems will be widely used. At present, long endurance is a major bottleneck in the development of fuel cell power systems. It has become the key to the development of long-endurance fuel cell power systems by greatly increasing the hydrogen storage density of hydrogen sources, thereby increasing the energy density of fuel cell power systems. However, the current mainstream high-pressure hydrogen cylinders cannot meet the needs of high energy density. Metal hydrides represented by sodium borohydride, magnesium hydride, calcium hydride and lithium hydride produce hydrogen through hydrolysis, and the hydrogen storage density can reach up to 25wt%, which is more than 7 times the hydrogen storage density of 35MPa high-pressure gas cylinders. It is the most advanced One of the revolutionary hydrogen source technologies.
水解制氢的应用也存在尚未完全解决的难题,关键问题之一是热量管理。水解反应释放大量的热量,如果无法顺利移走热量,将造成水解制氢体系温度升高。水解反应受到温度的影响较大,温度的升高对水解产氢速率有促进作用,可以提高产氢速度以及反应转化率,但温度过高不利于产氢速率的稳定控制,反应体系温度过高时存在反应失控的风险。目前,通过冷却水换热的方式进行温度调控,此方案造成了大量热量的浪费,例如,专利CN104555916B和CN101973520B等公开的水解制氢装置均通过冷却的方法进行换热,存在热量的浪费。而专利CN111533087A公开了速率可控水解制氢装置及控制方法,通过电流脉冲控制制氢速率,虽然制氢速率可控,但同样也造成了反应产热的浪费。There are also unsolved problems in the application of hydrogen production by hydrolysis, and one of the key issues is heat management. The hydrolysis reaction releases a large amount of heat. If the heat cannot be removed smoothly, the temperature of the hydrolysis hydrogen production system will rise. The hydrolysis reaction is greatly affected by temperature. The increase of temperature can promote the hydrogen production rate of hydrolysis, which can increase the hydrogen production rate and reaction conversion rate, but too high temperature is not conducive to the stable control of hydrogen production rate, and the reaction system temperature is too high There is a risk of uncontrolled reactions. At present, the temperature is regulated by means of cooling water heat exchange, which causes a lot of waste of heat. For example, the hydrolysis hydrogen production devices disclosed in patents CN104555916B and CN101973520B all perform heat exchange through cooling, and there is a waste of heat. The patent CN111533087A discloses a rate-controllable hydrolysis hydrogen production device and a control method. The hydrogen production rate is controlled by current pulses. Although the hydrogen production rate is controllable, it also causes waste of reaction heat generation.
然而,如何移走水解反应热并对反应热进行利用是水解制氢的技术难题,为此,本发明提出一种水解制氢系统。However, how to remove the heat of hydrolysis reaction and utilize the heat of reaction is a technical problem of hydrogen production by hydrolysis. Therefore, the present invention proposes a hydrogen production system by hydrolysis.
发明内容Contents of the invention
有鉴于此,有必要提供一种水解制氢系统及其使用方法,用以解决现有技术中如何移走水解反应热并对反应热进行利用的技术问题。In view of this, it is necessary to provide a hydrolysis hydrogen production system and its use method to solve the technical problem of how to remove the heat of hydrolysis reaction and utilize the heat of reaction in the prior art.
本发明通过下述技术方案实现:The present invention realizes through following technical scheme:
本发明提供了一种水解制氢系统,包括:The invention provides a hydrolysis hydrogen production system, comprising:
反应器,所述反应器内部形成有用于水解制氢反应发生的反应空间,所述反应器由导热材料制成。A reactor, wherein a reaction space for hydrogen production by hydrolysis is formed inside the reactor, and the reactor is made of a heat-conducting material.
供料组件,所述供料组件用于给所述反应空间分别通入第一反应物和第二反应物,所述第一反应物和第二反应物在所述反应空间内反应可产生氢气并放热。A feed assembly, the feed assembly is used to respectively feed the first reactant and the second reactant into the reaction space, and the first reactant and the second reactant react in the reaction space to generate hydrogen gas and exotherm.
发电组件,所述发电组件包括依次连接的相变储热层、温差电池组和散热翅片,所述相变储热层设于所述反应器的外侧壁,所述温差电池组设于所述相变储热层外侧,所述散热翅片设于所述温差电池组的外侧,所述温差电池组经由所述相变储热层和散热翅片的两端温度差进行温差发电。A power generation component, the power generation component includes a phase change heat storage layer, a thermoelectric battery group and cooling fins connected in sequence, the phase change heat storage layer is arranged on the outer wall of the reactor, and the thermoelectric battery group is arranged on the On the outside of the phase-change heat storage layer, the heat dissipation fins are arranged outside the thermoelectric battery group, and the thermoelectric battery group performs thermoelectric power generation through the temperature difference between the phase-change heat storage layer and the heat dissipation fins.
进一步的,所述相变储热层由铝合金或不锈钢材料制成,所述相变储热层为盒体结构且内部形成有容纳腔,所述容纳腔中填充有脂酸类有机物。Further, the phase-change heat storage layer is made of aluminum alloy or stainless steel, and the phase-change heat storage layer is a box structure with an accommodation cavity formed inside, and the accommodation cavity is filled with fatty acid organic matter.
进一步的,所述散热翅片由铜合金材料制成,所述散热翅片包括多个间隔分布的翅片本体。Further, the heat dissipation fins are made of copper alloy material, and the heat dissipation fins include a plurality of fin bodies distributed at intervals.
进一步的,所述第一反应物为金属氢化物。Further, the first reactant is a metal hydride.
进一步的,所述第二反应物为水溶液、乙二醇水溶液或甘油水溶液。Further, the second reactant is an aqueous solution, an aqueous ethylene glycol solution or an aqueous glycerin solution.
进一步的,所述的金属氢化物包括硼氢化钠、氢化镁、氢化钙或氢化锂中的至少一种。Further, the metal hydride includes at least one of sodium borohydride, magnesium hydride, calcium hydride or lithium hydride.
进一步的,所述金属氢化物被制成直径为3~8mm的小球。Further, the metal hydride is made into pellets with a diameter of 3-8mm.
进一步的,所述温差电池组由多个N型电极和P型电极组成,所述N型电极的材料为质量比为1:1的SiGe和GaP组成或质量比为1:1的Bi2Te3和GaP组成,所述P型电极的材料为SiGe或Bi2Te3。Further, the thermoelectric battery pack is composed of a plurality of N-type electrodes and P-type electrodes, and the material of the N-type electrodes is composed of SiGe and GaP with a mass ratio of 1:1 or Bi 2 Te with a mass ratio of 1:1 3 and GaP, and the material of the P-type electrode is SiGe or Bi 2 Te 3 .
进一步的,所述供料组件包括第一输料组件和第二输料组件,所述第一输料组件用于向所述反应空间通入金属氢化物;所述第二输料组件包括储液罐及泵体,所述储液罐用于储存水溶液、乙二醇水溶液或甘油水溶液,所述泵体用于将所述储液罐中的溶液输送至所述反应空间。Further, the feeding assembly includes a first feeding assembly and a second feeding assembly, the first feeding assembly is used to feed the metal hydride into the reaction space; the second feeding assembly includes a storage A liquid tank and a pump body, the liquid storage tank is used to store aqueous solution, ethylene glycol aqueous solution or glycerin aqueous solution, and the pump body is used to transport the solution in the liquid storage tank to the reaction space.
上述的任一项水解制氢系统的使用方法,包括以下步骤:The method for using any one of the above-mentioned hydrolysis hydrogen production systems includes the following steps:
S1:先将所述第一反应物和第二反应物分别通入所述反应空间内,所述第一反应物和第二反应物在所述反应空间内反应后产生氢气并放热。S1: firstly pass the first reactant and the second reactant into the reaction space respectively, and generate hydrogen and release heat after the first reactant and the second reactant react in the reaction space.
S2:所述相变储热层设于所述反应器的外侧壁以形成热端,所述散热翅片设于所述温差电池组的外侧且置于空气中以形成冷端,所述温差电池组经由所述热端和冷端的两端温度差进行温差发电。S2: The phase change heat storage layer is arranged on the outer wall of the reactor to form a hot end, the heat dissipation fin is arranged on the outer side of the thermoelectric battery pack and placed in the air to form a cold end, the temperature difference The battery pack performs thermoelectric power generation through the temperature difference between the hot end and the cold end.
本发明与现有技术相比,具有以下优点及有益效果:Compared with the prior art, the present invention has the following advantages and beneficial effects:
本发明通过设置所述反应器、供料组件和发电组件等零部件,先将所述第一反应物和第二反应物分别通入所述反应空间内,所述第一反应物和第二反应物在所述反应空间内反应后产生氢气并放热,所述相变储热层设于所述反应器的外侧壁以形成热端,所述散热翅片设于所述温差电池组的外侧且置于空气中以形成冷端,所述温差电池组经由所述热端和冷端的两端温度差进行温差发电,通过所述温差电池组可持续吸收反应产生的热量并利用,且能够使所述反应空间内的温度稳定,有利于持续稳定的制取氢气,设置所述相变储热层、温差电池组和散热翅片,一方面可通过热端持续吸收反应热并配合冷端进行发电,另一方面可通过所述散热翅片向空气中持续散除余热,以保证热端和冷端之间的温度差值稳定,有利于稳定的发电,因此,本发明通过设置上述结构,能够移走水解反应热并对反应热进行利用,避免造成能源的浪费。In the present invention, the first reactant and the second reactant are respectively passed into the reaction space by setting the parts such as the reactor, the feeding assembly and the power generation assembly, and the first reactant and the second reactant The reactants react in the reaction space to generate hydrogen and release heat. The phase change heat storage layer is arranged on the outer wall of the reactor to form a hot end, and the heat dissipation fins are arranged on the thermoelectric battery pack. outside and placed in the air to form a cold end, the thermoelectric battery pack performs thermoelectric power generation through the temperature difference between the hot end and the cold end, and the thermoelectric battery pack can continuously absorb and utilize the heat generated by the reaction, and can The temperature in the reaction space is stabilized, which is conducive to the continuous and stable production of hydrogen. The phase change heat storage layer, thermoelectric battery pack and heat dissipation fins are set. On the one hand, the hot end can continuously absorb the reaction heat and cooperate with the cold end. To generate electricity, on the other hand, the waste heat can be continuously dissipated into the air through the heat dissipation fins to ensure that the temperature difference between the hot end and the cold end is stable, which is conducive to stable power generation. Therefore, the present invention adopts the above-mentioned structure , can remove the heat of hydrolysis reaction and utilize the reaction heat, avoiding the waste of energy.
附图说明Description of drawings
图1为本发明提供的水解制氢系统一实施例的结构示意图。Fig. 1 is a structural schematic diagram of an embodiment of a hydrolysis hydrogen production system provided by the present invention.
附图标记:1、反应器;11、反应空间;2、供料组件;201、第一反应物;202、第二反应物;21、第二输料组件;211、储液罐;212、泵体;3、发电组件;31、相变储热层;32、温差电池组;33、散热翅片。Reference signs: 1. Reactor; 11. Reaction space; 2. Feed assembly; 201, first reactant; 202, second reactant; 21, second delivery assembly; 211, liquid storage tank; 212, 3. Power generation components; 31. Phase change heat storage layer; 32. Thermoelectric battery pack; 33. Radiating fins.
具体实施方式Detailed ways
下面结合附图来具体描述本发明优选实施例,附图构成本申请一部分,并与本发明实施例一起用于阐释本发明,并非用于限定本发明。The preferred embodiments of the present invention will be specifically described below in conjunction with the accompanying drawings. The accompanying drawings constitute a part of the application and are used together with the embodiments of the present invention to illustrate the present invention, but not to limit the present invention.
如图1所示,一种水解制氢系统,包括反应器1、供料组件2和发电组件3。As shown in FIG. 1 , a hydrolysis hydrogen production system includes a reactor 1 , a feed assembly 2 and a power generation assembly 3 .
所述反应器1内部形成有用于水解制氢反应发生的反应空间11,所述反应器1由导热材料制成。Inside the reactor 1 is formed a reaction space 11 for the hydrolysis reaction to produce hydrogen, and the reactor 1 is made of heat-conducting materials.
所述供料组件2用于给所述反应空间11分别通入第一反应物201和第二反应物202,所述第一反应物201和第二反应物202在所述反应空间11内反应可产生氢气并放热。The feed assembly 2 is used to feed the first reactant 201 and the second reactant 202 into the reaction space 11 respectively, and the first reactant 201 and the second reactant 202 react in the reaction space 11 Hydrogen gas is produced and is exothermic.
所述发电组件3包括依次连接的相变储热层31、温差电池组32和散热翅片33,所述相变储热层31设于所述反应器1的外侧壁,所述温差电池组32设于所述相变储热层31外侧,所述散热翅片33设于所述温差电池组32的外侧,所述温差电池组32经由所述相变储热层31和散热翅片33的两端温度差进行温差发电。The power generation assembly 3 includes a phase change heat storage layer 31, a thermoelectric battery pack 32 and a heat dissipation fin 33 connected in sequence, the phase change heat storage layer 31 is arranged on the outer wall of the reactor 1, and the thermoelectric battery pack 32 is arranged on the outside of the phase change heat storage layer 31, and the heat dissipation fins 33 are arranged on the outside of the thermoelectric battery pack 32, and the thermoelectric battery pack 32 passes through the phase change heat storage layer 31 and the heat dissipation fins 33 The temperature difference between the two ends of the power generation.
其中,所述第一反应物201和第二反应物202可以现有技术中的反应物,只要两者反应能够产生氢气并放热即可,例如,所述第一反应物201为质量比为2:1的氢化镁与硼氢化钠混合物,所述第二反应物202为水溶液、乙二醇水溶液或甘油水溶液,其中,当反应的环境温度为0℃以上时,所述第二反应物202可为水溶液、乙二醇水溶液或甘油水溶液三者中的任意一种,当反应的环境温度为0℃以下时,所述第二反应物202优选为乙二醇水溶液或甘油水溶液,这样设计可保证水溶液在反应过程中不结冰,有利于反应的稳定进行,特别的,只要现有技术中的各种反应物能够分别作为第一反应物201和第二反应物202进行反应,并产生氢气并放热,均可应用于本发明的水解制氢系统。Wherein, the first reactant 201 and the second reactant 202 can be reactants in the prior art, as long as the reaction between the two can generate hydrogen and release heat, for example, the first reactant 201 has a mass ratio of A 2:1 mixture of magnesium hydride and sodium borohydride, the second reactant 202 is an aqueous solution, an aqueous solution of ethylene glycol or an aqueous glycerin solution, wherein, when the ambient temperature of the reaction is above 0°C, the second reactant 202 It can be any one of aqueous solution, ethylene glycol aqueous solution or glycerin aqueous solution. When the ambient temperature of the reaction is below 0°C, the second reactant 202 is preferably ethylene glycol aqueous solution or glycerin aqueous solution. This design can Ensure that the aqueous solution does not freeze during the reaction, which is conducive to the stable progress of the reaction. In particular, as long as the various reactants in the prior art can react as the first reactant 201 and the second reactant 202 respectively, and generate hydrogen And exothermic, can be applied to the hydrolysis hydrogen production system of the present invention.
本发明通过设置所述反应器1、供料组件2和发电组件3等零部件,先将所述第一反应物201和第二反应物202分别通入所述反应空间11内,所述第一反应物201和第二反应物202在所述反应空间11内反应后产生氢气并放热,所述相变储热层31设于所述反应器1的外侧壁以形成热端,所述散热翅片33设于所述温差电池组32的外侧且置于空气中以形成冷端,所述温差电池组32经由所述热端和冷端的两端温度差进行温差发电,通过所述温差电池组32可持续吸收反应产生的热量并利用,且能够使所述反应空间11内的温度稳定,有利于持续稳定的制取氢气,设置所述相变储热层31、温差电池组32和散热翅片33,一方面可通过热端持续吸收反应热并配合冷端进行发电,另一方面可通过所述散热翅片33向空气中持续散除余热,以保证热端和冷端之间的温度差值稳定,有利于稳定的发电,因此,本发明通过设置上述结构,能够移走水解反应热并对反应热进行利用,避免造成能源的浪费。In the present invention, the first reactant 201 and the second reactant 202 are respectively passed into the reaction space 11 by setting the reactor 1, the feed assembly 2 and the power generation assembly 3 and other components, and the first reactant The first reactant 201 and the second reactant 202 react in the reaction space 11 to produce hydrogen and release heat. The phase change heat storage layer 31 is arranged on the outer wall of the reactor 1 to form a hot end. The cooling fins 33 are arranged on the outside of the thermoelectric battery pack 32 and placed in the air to form a cold end. The thermoelectric battery pack 32 performs thermoelectric power generation through the temperature difference between the hot end and the cold end. The battery pack 32 can continuously absorb and utilize the heat generated by the reaction, and can stabilize the temperature in the reaction space 11, which is conducive to the continuous and stable production of hydrogen. The phase change heat storage layer 31, the thermoelectric battery pack 32 and the The cooling fins 33, on the one hand, can continuously absorb the reaction heat through the hot end and cooperate with the cold end to generate electricity; The temperature difference is stable, which is conducive to stable power generation. Therefore, by setting the above structure, the present invention can remove the heat of hydrolysis reaction and utilize the heat of reaction to avoid waste of energy.
为了保证热端的温度值稳定不变以便于温差发电的稳定进行,所述相变储热层31由铝合金或不锈钢材料制成,所述相变储热层31为盒体结构且内部形成有容纳腔,所述容纳腔中填充有脂酸类有机物。通过设置所述相变储热层31和脂酸类有机物,使得所述相变储热层31在吸收反应热后的温度为恒定值,有利于温差发电的稳定进行。特别的,所述容纳腔还可填充石蜡或道生油等材料,理论上,只要是能够将吸收的反应热保持恒定的温度值的现有填充材料,也可应用于本发明。In order to ensure that the temperature value of the hot end is stable so as to facilitate the stable operation of thermoelectric power generation, the phase change heat storage layer 31 is made of aluminum alloy or stainless steel material, and the phase change heat storage layer 31 is a box structure with internally formed The accommodating chamber is filled with fatty acid organic matter. By arranging the phase-change heat storage layer 31 and fatty acid organic matter, the temperature of the phase-change heat storage layer 31 after absorbing the heat of reaction is constant, which is beneficial to stable thermoelectric power generation. In particular, the accommodating cavity can also be filled with materials such as paraffin wax or raw oil. In theory, as long as it is an existing filling material that can maintain the absorbed reaction heat at a constant temperature, it can also be applied to the present invention.
为了保证冷端的温度值稳定不变以便于温差发电的稳定进行,所述散热翅片33由铜合金材料制成,所述散热翅片33包括多个间隔分布的翅片本体。设置多个所述翅片本体一方面可加快温差发电速率,另一方面可通过多个所述翅片本体散除余热,以保证冷端的温度值稳定不变,有利于温差发电的稳定进行。In order to ensure that the temperature value of the cold end is stable so as to facilitate stable thermoelectric power generation, the heat dissipation fin 33 is made of copper alloy material, and the heat dissipation fin 33 includes a plurality of fin bodies distributed at intervals. On the one hand, arranging multiple fin bodies can speed up the rate of thermoelectric power generation, and on the other hand, the multiple fin bodies can dissipate waste heat to ensure that the temperature value of the cold end is stable, which is beneficial to the stable thermoelectric power generation.
为了能够移走水解反应热并对反应热进行利用,所述第一反应物201为金属氢化物。所述的金属氢化物包括硼氢化钠、氢化镁、氢化钙或氢化锂中的至少一种。所述第二反应物202为水溶液、乙二醇水溶液或甘油水溶液。所述金属氢化物被制成直径为3~8mm的小球。所述温差电池组32由多个N型电极和P型电极组成,所述N型电极的材料为质量比为1:1的SiGe和GaP组成或质量比为1:1的Bi2Te3和GaP组成,所述P型电极的材料为SiGe或Bi2Te3。所述供料组件2包括第一输料组件和第二输料组件21,所述第一输料组件用于向所述反应空间11通入金属氢化物;所述第二输料组件21包括储液罐211及泵体212,所述储液罐211用于储存水溶液、乙二醇水溶液或甘油水溶液,所述泵体212用于将所述储液罐211中的溶液输送至所述反应空间11。In order to remove the heat of hydrolysis reaction and utilize the heat of reaction, the first reactant 201 is a metal hydride. The metal hydride includes at least one of sodium borohydride, magnesium hydride, calcium hydride or lithium hydride. The second reactant 202 is an aqueous solution, an aqueous ethylene glycol solution or an aqueous glycerin solution. The metal hydride is made into pellets with a diameter of 3-8mm. The thermoelectric battery pack 32 is composed of a plurality of N-type electrodes and P-type electrodes, and the material of the N-type electrodes is composed of SiGe and GaP with a mass ratio of 1:1 or Bi2Te3 and GaP with a mass ratio of 1:1. The material of the P-type electrode is SiGe or Bi2Te3. The feeding assembly 2 includes a first feeding assembly and a
上述任一实施例中的水解制氢系统的使用方法,包括以下步骤:The method for using the hydrolysis hydrogen production system in any of the above embodiments includes the following steps:
S1:先将所述第一反应物201和第二反应物202分别通入所述反应空间11内,所述第一反应物201和第二反应物202在所述反应空间11内反应后产生氢气并放热。S1: first pass the first reactant 201 and the second reactant 202 into the reaction space 11 respectively, and the first reactant 201 and the second reactant 202 react in the reaction space 11 to produce Hydrogen and exothermic.
S2:所述相变储热层31设于所述反应器1的外侧壁以形成热端,所述散热翅片33设于所述温差电池组32的外侧且置于空气中以形成冷端,所述温差电池组32经由所述热端和冷端的两端温度差进行温差发电。S2: The phase change heat storage layer 31 is arranged on the outer wall of the reactor 1 to form a hot end, and the heat dissipation fin 33 is arranged on the outer side of the thermoelectric battery pack 32 and placed in air to form a cold end , the thermoelectric battery pack 32 performs thermoelectric power generation via the temperature difference between the hot end and the cold end.
本发明提供的水解制氢系统的具体应用例如下:The specific application examples of the hydrolysis hydrogen production system provided by the present invention are as follows:
实用例1:Use case 1:
先在反应器1内预装有质量比为2:1的氢化镁和硼氢化钠的复合小球,直径为3~4mm,所述反应器1的外壁从内至外依次设有相变储热层31、温差电池组32和散热翅片33,所述相变储热层31内填充相变石蜡,相变温度为70℃(相对于所述热端温度。),N极材料为质量比为1:1的SiGe和GaP组成,P极材料为SiGe。散热翅片33为多翅片结构,材质为无氧铜。Firstly, composite pellets of magnesium hydride and sodium borohydride with a mass ratio of 2:1 are pre-installed in the reactor 1, with a diameter of 3-4mm. The outer wall of the reactor 1 is sequentially provided with phase change storage Thermal layer 31, thermoelectric battery pack 32 and cooling fins 33, the phase change heat storage layer 31 is filled with phase change paraffin, the phase change temperature is 70°C (relative to the temperature of the hot end), and the N pole material is mass The composition of SiGe and GaP with a ratio of 1:1, and the material of the P pole is SiGe. The cooling fins 33 have a multi-fin structure and are made of oxygen-free copper.
工作环境温度为-40℃(相对于所述冷端温度。)时,所述储液罐211提供的为体积分数为54%的乙二醇水溶液,启动时外部为所述泵体212供电,泵体212以0.5L/min的速率将乙二醇水溶液注入到反应器1内,同时水解制氢反应开始,对外供氢量为3SL/min,此时反应器1壁温为70℃,环境空气温度为-40℃,温差电池组32发电功率为15W。When the working environment temperature is -40°C (relative to the temperature of the cold end), the
实用例2:Use case 2:
先在反应器1内预装有质量比为2:1的氢化镁和硼氢化钠的复合小球,直径为3~4mm,所述反应器1的外壁从内至外依次设有相变储热层31、温差电池组32和散热翅片33,所述相变储热层31内填充相变石蜡,相变温度为70℃(相对于所述热端温度。),N极材料为质量比为1:1的SiGe和GaP组成,P极材料为SiGe。散热翅片33为多翅片结构,材质为无氧铜。Firstly, composite pellets of magnesium hydride and sodium borohydride with a mass ratio of 2:1 are pre-installed in the reactor 1, with a diameter of 3-4mm. The outer wall of the reactor 1 is sequentially provided with phase change storage Thermal layer 31, thermoelectric battery pack 32 and cooling fins 33, the phase change heat storage layer 31 is filled with phase change paraffin, the phase change temperature is 70°C (relative to the temperature of the hot end), and the N pole material is mass The composition of SiGe and GaP with a ratio of 1:1, and the material of the P pole is SiGe. The cooling fins 33 have a multi-fin structure and are made of oxygen-free copper.
工作环境温度为-20℃(相对于所述冷端温度。)时,所述储液罐211提供的为体积分数为54%的乙二醇水溶液,启动时外部为水泵供电,水泵以0.5L/min的速率将乙二醇水溶液注入到反应器1内,启动水解制氢反应,对外供氢量为3SL/min,此时反应器1壁温为70℃,环境空气温度为-40℃,温差电池组32发电功率为12W。When the working environment temperature is -20°C (relative to the temperature of the cold end), the
实用例3:Use case 3:
先在反应器1内预装有质量比为2:1的氢化镁和硼氢化钠的复合小球,直径为3~4mm,所述反应器1的外壁从内至外依次设有相变储热层31、温差电池组32和散热翅片33,所述相变储热层31内填充相变石蜡,相变温度为70℃(相对于所述热端温度。),N极材料为质量比为1:1的SiGe和GaP组成,P极材料为SiGe。散热翅片33为多翅片结构,材质为无氧铜。Firstly, composite pellets of magnesium hydride and sodium borohydride with a mass ratio of 2:1 are pre-installed in the reactor 1, with a diameter of 3-4mm. The outer wall of the reactor 1 is sequentially provided with phase change storage Thermal layer 31, thermoelectric battery pack 32 and cooling fins 33, the phase change heat storage layer 31 is filled with phase change paraffin, the phase change temperature is 70°C (relative to the temperature of the hot end), and the N pole material is mass The composition of SiGe and GaP with a ratio of 1:1, and the material of the P pole is SiGe. The cooling fins 33 have a multi-fin structure and are made of oxygen-free copper.
工作环境温度为20℃(相对于所述冷端温度。)时,所述储液罐211提供的为体积分数为54%的乙二醇水溶液,启动时外部为水泵供电,水泵以0.5L/min的速率将水注入到反应器1内,启动水解制氢反应,对外供氢量为3SL/min,此时反应器1壁温为70℃,温差电池组32发电功率为10W,可供水泵用电10W。When the working environment temperature is 20° C. (relative to the temperature of the cold end), the
实用例4:Practical example 4:
先在反应器1内预装有质量比为2:1的氢化镁和硼氢化钠的复合小球,直径为4~6mm,所述反应器1的外壁从内至外依次设有相变储热层31、温差电池组32和散热翅片33,所述相变储热层31内填充相变石蜡,相变温度为70℃(相对于所述热端温度。),N极材料为质量比为1:1的SiGe和GaP组成,P极材料为SiGe。散热翅片33为多翅片结构,材质为无氧铜。Firstly, composite pellets of magnesium hydride and sodium borohydride with a mass ratio of 2:1 are pre-installed in the reactor 1, and the diameter is 4-6 mm. The outer wall of the reactor 1 is sequentially provided with phase change storage Thermal layer 31, thermoelectric battery pack 32 and cooling fins 33, the phase change heat storage layer 31 is filled with phase change paraffin, the phase change temperature is 70°C (relative to the temperature of the hot end), and the N pole material is mass The composition of SiGe and GaP with a ratio of 1:1, and the material of the P pole is SiGe. The cooling fins 33 have a multi-fin structure and are made of oxygen-free copper.
工作环境温度为-40℃(相对于所述冷端温度。)时,所述储液罐211提供的为体积分数为54%的乙二醇水溶液,启动时外部为所述泵体212供电,泵体212以0.5L/min的速率将乙二醇水溶液注入到反应器1内,同时水解制氢反应开始,对外供氢量为3SL/min,此时反应器1壁温为70℃,环境空气温度为-40℃,温差电池组32发电功率为14W。When the working environment temperature is -40°C (relative to the temperature of the cold end), the
实用例5:Practical example 5:
先在反应器1内预装有质量比为2:1的氢化镁和硼氢化钠的复合小球,直径为6~8mm,所述反应器1的外壁从内至外依次设有相变储热层31、温差电池组32和散热翅片33,所述相变储热层31内填充相变石蜡,相变温度为70℃(相对于所述热端温度。),N极材料为质量比为1:1的SiGe和GaP组成,P极材料为SiGe。散热翅片33为多翅片结构,材质为无氧铜。Firstly, composite pellets of magnesium hydride and sodium borohydride with a mass ratio of 2:1 are pre-installed in the reactor 1, with a diameter of 6-8 mm, and the outer wall of the reactor 1 is sequentially provided with phase change reservoirs. Thermal layer 31, thermoelectric battery pack 32 and cooling fins 33, the phase change heat storage layer 31 is filled with phase change paraffin, the phase change temperature is 70°C (relative to the temperature of the hot end), and the N pole material is mass The composition of SiGe and GaP with a ratio of 1:1, and the material of the P pole is SiGe. The cooling fins 33 have a multi-fin structure and are made of oxygen-free copper.
工作环境温度为-40℃(相对于所述冷端温度。)时,所述储液罐211提供的为体积分数为54%的乙二醇水溶液,启动时外部为所述泵体212供电,泵体212以0.5L/min的速率将乙二醇水溶液注入到反应器1内,同时水解制氢反应开始,对外供氢量为3SL/min,此时反应器1壁温为70℃,环境空气温度为-40℃,温差电池组32发电功率为12W。When the working environment temperature is -40°C (relative to the temperature of the cold end), the
综上所述,由实用例1、实用例2和实用例3可知,热端温度可通过所述相变储热层31及其容纳腔中的脂酸类有机物控制,当热端温度一定时,环境温度越低,所述冷端的温度也越低,因此能够增大所述温差电池组32的两端温差,能够增大发电的功率;由实用例1、实用例4和实用例5可知,热端温度可通过所述金属氢化物的直径大小控制,理论上,所述金属氢化物的直径大小越小,反应越是剧烈,导致反应不可控制,因此,实际应用中,调节所述金属氢化物的直径大小为3~8mm,有利于反应的稳定进行,当冷端温度一定时,所述金属氢化物的直径越大,反应越平稳,虽然发电功率有所减小,但是所述温差电池组32的两端温差较为稳定,便于反应的稳定进行。In summary, it can be seen from practical example 1, practical example 2 and practical example 3 that the temperature of the hot end can be controlled by the phase change heat storage layer 31 and the fatty acid organic matter in the containing chamber. When the temperature of the hot end is constant , the lower the ambient temperature, the lower the temperature of the cold end, so the temperature difference between the two ends of the thermoelectric battery pack 32 can be increased, and the power of power generation can be increased; it can be seen from practical example 1, practical example 4 and practical example 5 , the temperature at the hot end can be controlled by the diameter of the metal hydride. In theory, the smaller the diameter of the metal hydride, the more violent the reaction, resulting in an uncontrollable reaction. Therefore, in practical applications, adjusting the metal hydride The diameter of the hydride is 3-8mm, which is conducive to the stable progress of the reaction. When the temperature of the cold end is constant, the larger the diameter of the metal hydride, the more stable the reaction. Although the power generation is reduced, the temperature difference The temperature difference between the two ends of the battery pack 32 is relatively stable, which facilitates the stable progress of the reaction.
与现有技术相比,本发明所提供的水解制氢系统有以下有益效果:Compared with the prior art, the hydrolysis hydrogen production system provided by the present invention has the following beneficial effects:
本发明通过设置所述反应器1、供料组件2和发电组件3等零部件,先将所述第一反应物201和第二反应物202分别通入所述反应空间11内,所述第一反应物201和第二反应物202在所述反应空间11内反应后产生氢气并放热,所述相变储热层31设于所述反应器1的外侧壁以形成热端,所述散热翅片33设于所述温差电池组32的外侧且置于空气中以形成冷端,所述温差电池组32经由所述热端和冷端的两端温度差进行温差发电,通过所述温差电池组32可持续吸收反应产生的热量并利用,且能够使所述反应空间11内的温度稳定,有利于持续稳定的制取氢气,设置所述相变储热层31、温差电池组32和散热翅片33,一方面可通过热端持续吸收反应热并配合冷端进行发电,另一方面可通过所述散热翅片33向空气中持续散除余热,以保证热端和冷端之间的温度差值稳定,有利于稳定的发电,因此,本发明通过设置上述结构,能够移走水解反应热并对反应热进行利用,避免造成能源的浪费。In the present invention, the first reactant 201 and the second reactant 202 are respectively passed into the reaction space 11 by setting the reactor 1, the feed assembly 2 and the power generation assembly 3 and other components, and the first reactant The first reactant 201 and the second reactant 202 react in the reaction space 11 to produce hydrogen and release heat. The phase change heat storage layer 31 is arranged on the outer wall of the reactor 1 to form a hot end. The cooling fins 33 are arranged on the outside of the thermoelectric battery pack 32 and placed in the air to form a cold end. The thermoelectric battery pack 32 performs thermoelectric power generation through the temperature difference between the hot end and the cold end. The battery pack 32 can continuously absorb and utilize the heat generated by the reaction, and can stabilize the temperature in the reaction space 11, which is conducive to the continuous and stable production of hydrogen. The phase change heat storage layer 31, the thermoelectric battery pack 32 and the The cooling fins 33, on the one hand, can continuously absorb the reaction heat through the hot end and cooperate with the cold end to generate electricity; The temperature difference is stable, which is conducive to stable power generation. Therefore, by setting the above structure, the present invention can remove the heat of hydrolysis reaction and utilize the heat of reaction to avoid waste of energy.
以上所述,仅是本发明较佳实施例,并非对本发明任何形式上的限制,凡是依据本发明技术实质对以上实施例所作的任何简单修改、等同变化,均落入本发明保护范围之内。The above descriptions are only preferred embodiments of the present invention, and are not intended to limit the present invention in any form. All simple modifications and equivalent changes made to the above embodiments according to the technical essence of the present invention fall within the protection scope of the present invention. .
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4802929A (en) * | 1986-12-19 | 1989-02-07 | Fairchild Industries, Inc. | Compliant thermoelectric converter |
CN103515638A (en) * | 2012-06-28 | 2014-01-15 | 上海绿丽工贸有限公司 | Integrated hydrogen production-hydrogen storage power generation system |
CN106953548A (en) * | 2017-05-10 | 2017-07-14 | 华中科技大学 | A thermoelectric gas furnace based on Seebeck effect and phase change heat storage |
CN111533087A (en) * | 2020-05-25 | 2020-08-14 | 北京动力京工科技有限公司 | Catalyst-free rate-controllable hydrolysis hydrogen production device and control method thereof |
CN115011921A (en) * | 2022-05-25 | 2022-09-06 | 华南师范大学 | Germanium selenide film with micro-hollow brick structure, solar power generation and hydrolysis hydrogen production device and preparation method thereof |
-
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4802929A (en) * | 1986-12-19 | 1989-02-07 | Fairchild Industries, Inc. | Compliant thermoelectric converter |
CN103515638A (en) * | 2012-06-28 | 2014-01-15 | 上海绿丽工贸有限公司 | Integrated hydrogen production-hydrogen storage power generation system |
CN106953548A (en) * | 2017-05-10 | 2017-07-14 | 华中科技大学 | A thermoelectric gas furnace based on Seebeck effect and phase change heat storage |
CN111533087A (en) * | 2020-05-25 | 2020-08-14 | 北京动力京工科技有限公司 | Catalyst-free rate-controllable hydrolysis hydrogen production device and control method thereof |
CN115011921A (en) * | 2022-05-25 | 2022-09-06 | 华南师范大学 | Germanium selenide film with micro-hollow brick structure, solar power generation and hydrolysis hydrogen production device and preparation method thereof |
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