WO2021208013A1 - Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction - Google Patents
Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction Download PDFInfo
- Publication number
- WO2021208013A1 WO2021208013A1 PCT/CN2020/085118 CN2020085118W WO2021208013A1 WO 2021208013 A1 WO2021208013 A1 WO 2021208013A1 CN 2020085118 W CN2020085118 W CN 2020085118W WO 2021208013 A1 WO2021208013 A1 WO 2021208013A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- catalyst carrier
- catalyst
- layer
- reactant
- metal particles
- 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.)
- Ceased
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
- B01J35/45—Nanoparticles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0217—Pretreatment of the substrate before coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0221—Coating of particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/024—Multiple impregnation or coating
- B01J37/0244—Coatings comprising several layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0219—Coating the coating containing organic compounds
Definitions
- the present invention relates to a method for manufacturing a catalyst reactant with high-efficiency catalysis of thermal reaction, and particularly refers to a catalyst reactant applied to a catalyst-catalyzed gas-phase reaction system to improve the combustion reaction of the fuel provided in the catalyst-catalyzed gas-phase reaction system Catalytically active substance.
- a heating system for catalyst-catalyzed gas-phase reaction which is mainly used in the heating system equipped with multiple catalyst reactants in the reaction furnace, and the multiple catalyst reactants that have been heated in the reactor It can form a continuous thermal reaction with the fuel, and the heat energy generated by the multiple reactants formed by the thermal reaction is used to continuously heat the liquid stored in the reactor.
- This constitutes a heating system It can be used as power or heat source for various purposes, so that it does not need to be heated by open flame combustion, completely avoiding carbonized particles or toxic gases generated during combustion, thereby effectively improving air quality.
- the existing heating system for catalyst-catalyzed gas-phase reaction uses a catalyst reactant composed of a single material and a single layer of nano metal particles, so that the existing catalyst reactant must be heated to a relatively high temperature.
- High temperature can be used for thermal reaction with fuel, and its oxidation efficiency is also low. Therefore, the thermal reaction efficiency cannot be effectively or better greatly improved.
- the purpose of the present invention is to provide a method for producing a catalyst reactant with high efficiency catalysis of thermal reaction.
- the catalyst reactant of the present invention is particularly applied to a catalyst catalytic gas phase reaction system to serve as an elevated catalyst catalytic gas phase reaction system.
- the catalytic activity of the internal fuel combustion reaction, and the preparation method of the catalyst reactant includes:
- Step 2 Prepare at least one aqueous nano metal particle solution
- Step 3 Surface modification of the catalyst carrier: soak the catalyst carrier in a methanol solution containing 1-15% silanyl compound, and let it stand for 1 to 3 hours, then take out the catalyst carrier and clean it with a cleaning solution, and then apply the catalyst carrier Dry the program and send it to the refrigeration program;
- Step 5 The surface of the catalyst carrier is then joined with multiple layers of nano metal particles:
- the catalyst carrier with the first layer of metal nano particles on the surface is immersed in a methanol solution containing 3-25% lauryl amino alcohol. Modification, take out the modified catalyst carrier with the first layer of nano metal particles to dry, and then soak it in the prepared aqueous nano metal particle solution, let it stand for 1 to 3 hours, then take out the bonded
- the catalyst carrier with the first layer of nano metal particles is cleaned with a cleaning solution, and then the catalyst carrier with the first layer of nano metal particles is dried to complete the first layer of nano metal particles.
- the surface of the catalyst carrier is joined to form a second layer of nano metal particles.
- step 5 can be repeated, so that the catalyst carrier with the second layer of nano metal particles can have multiple layers of nano metal particles formed on its surface.
- water-phase nano metal particle solution in step 3 and step 5 can be made of the same metal particle material, so that the material of each layer of the catalyst carrier is the same.
- water-phase nano metal particle solution in step 3 and step 5 may be made of different metal particle materials, so that the material of each layer of nano metal particles of the catalyst carrier is different.
- water-phase nano metal particle solution in step 3 and step 5 may be partly of the same metal particle material, so that the material of each layer of the catalyst carrier can be partly the same or partly different.
- the catalyst reactant completed in step 5 is used to be set on a placing tray, the placing tray is provided with a plurality of holding grooves arranged at equal intervals, and at least one through hole is provided around the holding groove. The through hole is communicated with the holding groove, so that the catalyst reactant forms an evenly spaced arrangement on the placing plate.
- the oxide in step 1 may be any one or a combination of silicon dioxide, aluminum oxide, titanium dioxide, zirconium dioxide, silicon carbide, and aluminum nitride.
- silyl compound in step 3 may be any one of 3-aminopropyltriethoxysilane, trimethoxysilane, or dimethoxy-ethylsilane.
- the cleaning solution can be one of ionized water or alcohol.
- step 3 is to put the catalyst carrier after the cleaning has been completed into an oven at 80°C to 90°C for 20 to 40 minutes, then take it out and place it at room temperature for cooling, and the refrigeration procedure is to be completed
- the catalyst carrier in the drying process is placed in a test tube filled with nitrogen and placed in a refrigerator for refrigeration.
- step 5 is to place the catalyst carrier with the first layer of nano metal particles in a test tube and place it in an oven at 80°C to 90°C for drying.
- Fig. 1 A flow chart of the method for preparing the catalyst reactant with high efficiency catalysis of thermal reaction according to the present invention.
- Figure 2 A cross-sectional schematic diagram of a catalyst-catalyzed gas phase reaction system of the present invention.
- Figure 3 The enlarged schematic diagram of the circle A in Figure 2 of the present invention.
- the present invention discloses a method for making a catalyst reactant with high efficiency catalysis of thermal reaction.
- the catalyst reactant 1 is especially applied to a catalyst catalyzed gas phase reaction system 2 .
- the preparation method of the catalyst reactant 1 includes:
- Step 1 Preparation of catalyst carrier: At least one oxide is made into a catalyst powder, and then the catalyst powder is granulated to form a three-dimensional shape (such as a sphere, a cylinder, a cube or a rectangular parallelepiped and other three-dimensional shapes) Catalyst carrier.
- the oxide can be any one or more combination (composite) oxides such as silicon dioxide, aluminum oxide, titanium dioxide, zirconium dioxide, silicon carbide, aluminum nitride and the like.
- Step 3 Surface modification of the catalyst carrier:
- the catalyst carrier of step 1 is soaked in methanol solution containing 1-15% silanyl compound, and after standing for 1 to 3 hours, the catalyst carrier is taken out and cleaned with a cleaning solution, and then The catalyst carrier undergoes a drying process and is sent to a refrigeration process.
- Step 4 Join the first layer of nano metal particles on the surface of the catalyst carrier: soak the modified catalyst carrier in the aqueous nano metal particle solution prepared in step 2, and let it stand for 1 to 3 hours, then take out the catalyst carrier It is cleaned with a cleaning solution, and then the catalyst carrier is blow-dried. That is, the surface of the catalyst carrier is joined to form the first layer of nano metal particles.
- the cleaning solution may be ionized water or alcohol.
- the cleaned catalyst carrier can be dried by nitrogen.
- Step 5 The surface of the catalyst carrier is then joined with multiple layers of nano metal particles:
- the surface of the catalyst carrier with the first layer of nano metal particles is immersed in the catalyst carrier containing 3 ⁇ 25% dodecaneamino alcohol (1,12-dodecaneamino). , Abbreviated as 1,12 DDCA) in methanol solution for modification, take out the modified catalyst carrier bonded with the first layer of nano metal particles for drying process, and then soak in the water phase nano metal particles prepared in step 2.
- 1,12 DDCA dodecaneamino alcohol
- the drying procedure of the step 5 is to place the catalyst carrier with the first layer of nano metal particles in a test tube and put it in an oven at 80°C to 90°C for drying.
- the cleaning solution may be ionized water or alcohol.
- the cleaned catalyst carrier can be dried by nitrogen.
- the present invention can repeat step 5, so that the catalyst carrier that has a second layer of nano metal particles can have multiple layers (such as the third layer, the fourth layer, and so on) formed on the surface of the catalyst carrier; in addition, ,
- the aqueous nano metal particle solution in step 3 and step 5 can be the same metal particle material or different metal particle material, so that the material of each layer of the catalyst carrier can be the same, Some of the same or all of them are different, so that the surface of the catalyst carrier with the first layer of nano-metal particles can be formed with multiple layers of single-component (or multiple-component) nano-metal particles.
- the material of the first layer and the second layer (or multiple layers) of the catalyst carrier can be nano-gold particles; the material of the first layer of the catalyst carrier can be nano-metal particles.
- the material of the rice gold particles, and the second layer (or other layer) of the nano metal particles can be nano platinum particles; the material of the first layer of the catalyst carrier can be nano metal particles.
- Particles, and the material of the second layer of nano metal particles can be nano platinum particles, and the material of other layers of nano metal particles can be nano silver particles (or nano metal particles of other materials).
- the placing tray 3 can be set in the reaction furnace 21 provided in the catalytic gas phase reaction system 2.
- the heater 22 provided in the reaction furnace 21 first heats the catalyst reactant 1 and when the catalyst reactant 1 reaches one When the temperature is preset, the heater 22 can be turned off; at this time, the fuel inside the fuel tank 23 (may be other fuels such as methanol, ethanol, isopropanol, or methane) passes through the fuel pipe 231, the atomizer 232, and The atomizer 232 atomizes and sprays the fuel in the reactor 21, so that the fuel sprayed from the atomizer 232 can pass through the through hole 32 of each receiving groove 31, so that the fuel can be evenly distributed in each
- the catalyst reactant 1 enables a plurality of catalyst reactants 1 to react with the fuel to form a better and continuous thermal reaction.
- the technical feature of the present invention is to use a methanol solution containing 1,12-dodecaneamino (1,12 DDCA for short) to modify the catalyst carrier that has the first layer of nano metal particles. Afterwards, it is immersed in an aqueous nano-metal particle solution of the same or different metal materials, so that the surface of the catalyst carrier with the first layer of nano-metal particles is joined to form a second layer of nano-metal particles; Repeat this step so that the catalyst carrier with the first layer of nano metal particles can have multiple layers of single component (or multiple and multiple composite components) nano metal particles formed on the surface; reaching a catalyst with multiple layers of nano metal particles
- the reactant can use the interface metal between the particles (ie, the supporting force effect) to enhance the catalytic activity of the fuel combustion reaction, so that the catalyst reactant can have a lower ignition temperature and high oxidation efficiency; at the same time, it can use a variety of The catalyst reactant 1 of nano metal particles can have better thermal reaction catalyst performance, and the catalyst reactant 1
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Catalysts (AREA)
Abstract
Description
本发明有关一种具热反应高效催化的触媒反应物的制作方法,特别专指一种触媒反应物应用于一触媒催化气相反应系统,以作为提升触媒催化气相反应系统内部所设燃料燃烧反应的催化活性物质。 The present invention relates to a method for manufacturing a catalyst reactant with high-efficiency catalysis of thermal reaction, and particularly refers to a catalyst reactant applied to a catalyst-catalyzed gas-phase reaction system to improve the combustion reaction of the fuel provided in the catalyst-catalyzed gas-phase reaction system Catalytically active substance.
在目前工商发达时代,人类赖以维生的空气,正因工业燃烧废气、交通工具所排放的气体,慢性地伤害人们的健康,主因乃是空气中的有害悬浮微粒,除会引发各种呼吸系统与过敏疾病,更会影响居家品质与工作效率,近年来空气品质议题逐渐受到世人所重视。In the current age of industrial and commercial development, the air that humans rely on for their livelihood is chronically harming people’s health due to industrial combustion exhaust gas and the gas emitted by vehicles. The main reason is the harmful suspended particles in the air, which in addition to cause various breathing System and allergic diseases will even affect home quality and work efficiency. In recent years, air quality issues have gradually attracted the attention of the world.
就传统的大型供暖设备需燃烧大量煤来制造热能,而燃烧过程所产生的大量碳化粒子,必然会造成空气污染,使得大气中的细悬浮微粒(PM2.5,直径≦2.5微米)不断增加,所危害人类健康,已是不分国界与疆域,近数十年世界各国对于空气污染议题,更是不遗余力,寻求改善的方法。Traditional large-scale heating equipment needs to burn a large amount of coal to produce heat, and the large amount of carbonized particles produced during the combustion process will inevitably cause air pollution, causing the fine suspended particulates (PM2.5, diameter ≦2.5 microns) in the atmosphere to continue to increase. Human health is endangered regardless of national borders and territories. In recent decades, countries in the world have spared no effort in addressing air pollution issues and seeking ways to improve.
有鉴于此,研发出一种触媒催化气相反应的供热系统,其主要利用于供热系统所设置的反应炉内设有多个触媒反应物,通过反应炉内已加热的多个触媒反应物能与燃料形成持续性的热反应,再由所形成热反应的多个反应物产生的热能,用以对反应炉内所储设的液体,进行持续性的加热,此所构成的供热系统,以能作为动力或提供热源等各种用途,达到不需以明火燃烧方式进行加热,完全避免燃烧时所产生的碳化粒子或有毒气体,借以有效改善空气品质。In view of this, a heating system for catalyst-catalyzed gas-phase reaction was developed, which is mainly used in the heating system equipped with multiple catalyst reactants in the reaction furnace, and the multiple catalyst reactants that have been heated in the reactor It can form a continuous thermal reaction with the fuel, and the heat energy generated by the multiple reactants formed by the thermal reaction is used to continuously heat the liquid stored in the reactor. This constitutes a heating system , It can be used as power or heat source for various purposes, so that it does not need to be heated by open flame combustion, completely avoiding carbonized particles or toxic gases generated during combustion, thereby effectively improving air quality.
然而,现有触媒催化气相反应的供热系统,所使用的触媒反应物,乃由单一种材质和单层奈米金属粒子所组合的触媒反应物,使得现有触媒反应物,必须加热至较高温度,才能与燃料进行热反应,同时其氧化效率也较低,因此热反应效率无法有效或更佳地大幅提升。However, the existing heating system for catalyst-catalyzed gas-phase reaction uses a catalyst reactant composed of a single material and a single layer of nano metal particles, so that the existing catalyst reactant must be heated to a relatively high temperature. High temperature can be used for thermal reaction with fuel, and its oxidation efficiency is also low. Therefore, the thermal reaction efficiency cannot be effectively or better greatly improved.
因此,如何研发一种具多种复合成份奈米金属粒子的触媒反应物,让触媒反应物能具有更低的起燃温度以及高氧化效率,即为本发明所欲解决的主要课题。Therefore, how to develop a catalyst reactant with multiple composite nano-metal particles so that the catalyst reactant can have a lower ignition temperature and high oxidation efficiency is the main problem to be solved by the present invention.
本发明的目的在于提供一种具热反应高效催化的触媒反应物的制作方法,本发明所述的触媒反应物,尤其指应用于一触媒催化气相反应系统,以作为提升触媒催化气相反应系统其内部所设燃料燃烧反应的催化活性,触媒反应物其制作方法包括:The purpose of the present invention is to provide a method for producing a catalyst reactant with high efficiency catalysis of thermal reaction. The catalyst reactant of the present invention is particularly applied to a catalyst catalytic gas phase reaction system to serve as an elevated catalyst catalytic gas phase reaction system. The catalytic activity of the internal fuel combustion reaction, and the preparation method of the catalyst reactant includes:
步骤1、触媒载体制备:将至少一种氧化物制作一触媒粉体,再将触媒粉体进行造粒程序而形成具立体状的触媒载体;Step 1. Preparation of catalyst carrier: at least one oxide is made into a catalyst powder, and then the catalyst powder is granulated to form a three-dimensional catalyst carrier;
步骤2、制备至少一种水相奈米金属粒子溶液;Step 2. Prepare at least one aqueous nano metal particle solution;
步骤3、触媒载体表面修饰:将触媒载体浸泡于含有1~15%硅烷基化合物的甲醇溶液中,以静置1~3小时后,取出触媒载体并以清洗溶液进行清洗,再将触媒载体进行烘干程序并送至冷藏程序;Step 3. Surface modification of the catalyst carrier: soak the catalyst carrier in a methanol solution containing 1-15% silanyl compound, and let it stand for 1 to 3 hours, then take out the catalyst carrier and clean it with a cleaning solution, and then apply the catalyst carrier Dry the program and send it to the refrigeration program;
步骤4、触媒载体表面接合第一层奈米金属粒子:将表面完成修饰的触媒载体浸泡于已制备的水相奈米金属粒子溶液中,以静置1~3小时后,取出触媒载体并以清洗溶液进行清洗,再将触媒载体进行吹干,即完成触媒载体的表面接合形成有第一层奈米金属粒子;Step 4. Join the first layer of nano metal particles on the surface of the catalyst carrier: Immerse the surface-modified catalyst carrier in the prepared aqueous nano metal particle solution, and then let it stand for 1 to 3 hours, then take out the catalyst carrier and The cleaning solution is used for cleaning, and then the catalyst carrier is blown dry, that is, the surface of the catalyst carrier is joined to form the first layer of nano metal particles;
步骤5、触媒载体表面再接合多层奈米金属粒子:将表面完成接合有第一层奈米金属粒子的触媒载体,浸泡于含有3~25%十二烷基氨基醇的甲醇溶液中以进行修饰,取出已修饰的接合有第一层奈米金属粒子的触媒载体进行烘干程序,再浸泡于已制备的水相奈米金属粒子溶液中,以静置1~3小时后,取出已接合有第一层奈米金属粒子的触媒载体并以清洗溶液进行清洗,再将已接合有第一层奈米金属粒子的触媒载体进行吹干,即完成已接合有第一层奈米金属粒子的触媒载体,其表面再接合形成有第二层奈米金属粒子。Step 5. The surface of the catalyst carrier is then joined with multiple layers of nano metal particles: The catalyst carrier with the first layer of metal nano particles on the surface is immersed in a methanol solution containing 3-25% lauryl amino alcohol. Modification, take out the modified catalyst carrier with the first layer of nano metal particles to dry, and then soak it in the prepared aqueous nano metal particle solution, let it stand for 1 to 3 hours, then take out the bonded The catalyst carrier with the first layer of nano metal particles is cleaned with a cleaning solution, and then the catalyst carrier with the first layer of nano metal particles is dried to complete the first layer of nano metal particles. The surface of the catalyst carrier is joined to form a second layer of nano metal particles.
进一步的,步骤5可以重复进行,让已具第二层奈米金属粒子的该触媒载体其表面可形成有多层奈米金属粒子。Further, step 5 can be repeated, so that the catalyst carrier with the second layer of nano metal particles can have multiple layers of nano metal particles formed on its surface.
进一步的,步骤3及步骤5的该水相奈米金属粒子溶液,可以是相同金属粒子材质,使该触媒载体其每一层奈米金属粒子的材质皆相同。Furthermore, the water-phase nano metal particle solution in step 3 and step 5 can be made of the same metal particle material, so that the material of each layer of the catalyst carrier is the same.
进一步的,步骤3及步骤5的该水相奈米金属粒子溶液,可以是不相同金属粒子材质,使该触媒载体其每一层奈米金属粒子的材质皆不相同。Further, the water-phase nano metal particle solution in step 3 and step 5 may be made of different metal particle materials, so that the material of each layer of nano metal particles of the catalyst carrier is different.
进一步的,步骤3及步骤5的该水相奈米金属粒子溶液,可以是部分相同金属粒子材质,使该触媒载体其每一层奈米金属粒子的材质可以部分相同及部分不相同。Furthermore, the water-phase nano metal particle solution in step 3 and step 5 may be partly of the same metal particle material, so that the material of each layer of the catalyst carrier can be partly the same or partly different.
进一步的,步骤5完成的该触媒反应物,用以设置于一放置盘,该放置盘设有多个等距间隔排列的承置槽,该承置槽其周围设有至少一透孔,该透孔与该承置槽形成相通,使该触媒反应物于该放置盘上形成等距间隔排列形式。Further, the catalyst reactant completed in step 5 is used to be set on a placing tray, the placing tray is provided with a plurality of holding grooves arranged at equal intervals, and at least one through hole is provided around the holding groove. The through hole is communicated with the holding groove, so that the catalyst reactant forms an evenly spaced arrangement on the placing plate.
进一步的,步骤1的该氧化物,可以是二氧化硅、三氧化二铝、二氧化钛、二氧化锆、碳化硅、氮化铝中的任意一种或多种的组合。Further, the oxide in step 1 may be any one or a combination of silicon dioxide, aluminum oxide, titanium dioxide, zirconium dioxide, silicon carbide, and aluminum nitride.
进一步的,步骤3的该硅烷基化合物,可以是3-氨基丙基三乙氧基硅烷、三甲氧基硅烷或二甲氧基一乙基硅烷的任意一种。Further, the silyl compound in step 3 may be any one of 3-aminopropyltriethoxysilane, trimethoxysilane, or dimethoxy-ethylsilane.
进一步的,清洗溶液,可以是离子水或酒精中的一种。Further, the cleaning solution can be one of ionized water or alcohol.
进一步的,步骤3的烘干程序,为将已清洗完成后的该触媒载体放入80℃~90℃烘箱中并进行20 ~40分钟后,取出放置室温冷却,且该冷藏程序为将已完成烘干程序的该触媒载体,置入具氮气填充的试管中并置于一冰箱进行冷藏。Further, the drying procedure in step 3 is to put the catalyst carrier after the cleaning has been completed into an oven at 80°C to 90°C for 20 to 40 minutes, then take it out and place it at room temperature for cooling, and the refrigeration procedure is to be completed The catalyst carrier in the drying process is placed in a test tube filled with nitrogen and placed in a refrigerator for refrigeration.
进一步的,步骤5的烘干程序,为将接合有第一层奈米金属粒子的该触媒载体放置于试管中并置入80℃~90℃烘箱烘干。Further, the drying procedure in step 5 is to place the catalyst carrier with the first layer of nano metal particles in a test tube and place it in an oven at 80°C to 90°C for drying.
本发明的技术特征在于,利用含有十二烷基氨基醇的甲醇溶液,再对已具第一层奈米金属粒子的触媒载体进行修饰;之后,再浸泡于相同或不相同金属材质的水相奈米金属粒子溶液中,使已具第一层奈米金属粒子的触媒载体其表面再接合形成有第二层奈米金属粒子,如此可重复此步骤,让具第一层奈米金属粒子的触媒载体其表面,可形成有多层单一成份(或多种复合成份)奈米金属粒子,达到具多层奈米金属粒子的触媒反应物,可以利用粒子之间的界面金属(即担体作用力效应)来提升燃料燃烧反应的催化活性,让触媒反应物能具有更低的起燃温度以及高氧化效率,大幅提升其热反应效率。The technical feature of the present invention is to use a methanol solution containing dodecylamino alcohol to modify the catalyst carrier that has the first layer of nano metal particles; then, it is immersed in an aqueous phase of the same or different metal materials. In the nano metal particle solution, the surface of the catalyst carrier that has the first layer of nano metal particles is joined to form a second layer of nano metal particles. This step can be repeated to make the catalyst carrier with the first layer of nano metal particles The surface of the catalyst carrier can be formed with multiple layers of single-component (or multiple composite components) nano-metal particles to reach a catalyst reactant with multiple layers of nano-metal particles. The interface metal between the particles (that is, the supporting force) Effect) to improve the catalytic activity of the fuel combustion reaction, so that the catalyst reactant can have a lower ignition temperature and high oxidation efficiency, and greatly improve its thermal reaction efficiency.
下面结合附图和具体实施方式对本发明作进一步详细的说明。The present invention will be further described in detail below in conjunction with the drawings and specific embodiments.
图1:本发明具热反应高效催化的触媒反应物的制作方法一流程图。Fig. 1: A flow chart of the method for preparing the catalyst reactant with high efficiency catalysis of thermal reaction according to the present invention.
图2:本发明试举一触媒催化气相反应系统的剖面示意图。Figure 2: A cross-sectional schematic diagram of a catalyst-catalyzed gas phase reaction system of the present invention.
图3:本发明的图2示中A圈式处放大示意图。Figure 3: The enlarged schematic diagram of the circle A in Figure 2 of the present invention.
附图标记说明Description of Reference Signs
1、触媒反应物1. Catalyst reactant
2、触媒催化气相反应系统2. Catalyst catalyzed gas phase reaction system
21、反应炉21. Reactor
22、加热器22. Heater
23、燃料桶23. Fuel barrels
231、燃料管231. Fuel Pipe
232、雾化器232、Atomizer
3、放置盘3. Place the plate
31、承置槽31, holding trough
32、透孔。32. Through holes.
为使更方便简捷了解本发明的其他特征内容与优点及其所达成的功效能够更为显现,现将本发明配合附图,详细叙述本发明的特征以及优点,以下的各实施例进一步详细说明本发明的观点,但非以任何观点限制本发明的范畴。In order to make it more convenient and simple to understand the other features and advantages of the present invention and the effects achieved by it, the present invention will now be combined with the accompanying drawings to describe the features and advantages of the present invention in detail. The following embodiments are further described in detail. The viewpoint of the present invention does not limit the scope of the present invention by any viewpoint.
请先参阅图1、图2和图3所示,本发明公开一种具热反应高效催化的触媒反应物的制作方法,所述触媒反应物1尤其指是应用于一触媒催化气相反应系统2,以作为提升触媒催化气相反应系统2其内部所设燃料燃烧反应的催化活性,所述触媒反应物1其制作方法包括:Please refer to Figure 1, Figure 2 and Figure 3, the present invention discloses a method for making a catalyst reactant with high efficiency catalysis of thermal reaction. The catalyst reactant 1 is especially applied to a catalyst catalyzed gas phase reaction system 2 , In order to improve the catalytic activity of the fuel combustion reaction of the catalyst-catalyzed gas-phase reaction system 2, and the preparation method of the catalyst reactant 1 includes:
步骤1:触媒载体制备:将至少一种氧化物制作一触媒粉体,再将触媒粉体进行造粒程序而形成具立体状(如:球体、柱体、正方体或长方体等其它立体形状)的触媒载体。所述的氧化物可以是二氧化硅、三氧化二铝、二氧化钛、二氧化锆、碳化硅、氮化铝等任意一种或多种组合(复合)的氧化物。Step 1: Preparation of catalyst carrier: At least one oxide is made into a catalyst powder, and then the catalyst powder is granulated to form a three-dimensional shape (such as a sphere, a cylinder, a cube or a rectangular parallelepiped and other three-dimensional shapes) Catalyst carrier. The oxide can be any one or more combination (composite) oxides such as silicon dioxide, aluminum oxide, titanium dioxide, zirconium dioxide, silicon carbide, aluminum nitride and the like.
步骤2:制备至少一种水相奈米金属粒子溶液,所述水相奈米金属粒子溶液的奈米金属粒子材质可以是金、银、钯、铑、钌或铱等其它金属材质;另外,所述步骤2可制备两种或两种以上不同奈米金属材质的水相奈米金属粒子溶液。Step 2: Prepare at least one water-phase nano metal particle solution. The nano metal particle material of the water-phase nano metal particle solution can be other metal materials such as gold, silver, palladium, rhodium, ruthenium or iridium; in addition, The step 2 can prepare two or more aqueous nanometal particle solutions of different nanometal materials.
步骤3:触媒载体表面修饰:将步骤1的触媒载体浸泡于含有1~15%硅烷基化合物的甲醇溶液中,以静置1~3小时后,取出触媒载体并以清洗溶液进行清洗,再将触媒载体进行烘干程序并送至冷藏程序。所述硅烷基化合物可以是3-氨基丙基三乙氧基硅烷 (3-Aminopropyl)trimethoxysilane ,简称APTMS)、(3-硫基丙基)三甲氧基硅烷 (3-Mercaptopropyl)trimethoxysilane ,简称MPTMS)或(3-硫基甲基)二甲氧基一乙基硅烷 (mercaptomethyl-dimethylethoxy silane ,简称MMDMES)。所述清洗溶液可以是离子水或酒精。所述烘干程序为将已清洗完成后的触媒载体放入80℃~90℃烘箱中并进行20~40分钟后,取出放置室温冷却。所述冷藏程序将已完成烘干程序的触媒载体,置入具氮气填充的试管中并置于一冰箱进行冷藏。Step 3: Surface modification of the catalyst carrier: The catalyst carrier of step 1 is soaked in methanol solution containing 1-15% silanyl compound, and after standing for 1 to 3 hours, the catalyst carrier is taken out and cleaned with a cleaning solution, and then The catalyst carrier undergoes a drying process and is sent to a refrigeration process. The silyl compound may be 3-aminopropyltriethoxysilane (3-Aminopropyl)trimethoxysilane, APTMS for short), (3-thiopropyl)trimethoxysilane (3-Mercaptopropyl)trimethoxysilane, MPTMS for short) or (3-thiomethyl)dimethoxy-ethyl silane (mercaptomethyl-dimethylethoxy silane , MMDMES for short). The cleaning solution may be ionized water or alcohol. The drying procedure is to put the cleaned catalyst carrier into an oven at 80°C to 90°C for 20 to 40 minutes, and then take it out to cool at room temperature. In the refrigerating procedure, the catalyst carrier that has completed the drying procedure is placed in a test tube filled with nitrogen and placed in a refrigerator for refrigeration.
步骤4:触媒载体表面接合第一层奈米金属粒子:将表面完成修饰的触媒载体浸泡于步骤2已制备的水相奈米金属粒子溶液中,以静置1~3小时后,取出触媒载体并以清洗溶液进行清洗,再将触媒载体进行吹干,即完成触媒载体的表面接合形成有第一层奈米金属粒子。所述清洗溶液可以是离子水或酒精。所述已清洗完成的触媒载体可由氮气进行吹干。Step 4: Join the first layer of nano metal particles on the surface of the catalyst carrier: soak the modified catalyst carrier in the aqueous nano metal particle solution prepared in step 2, and let it stand for 1 to 3 hours, then take out the catalyst carrier It is cleaned with a cleaning solution, and then the catalyst carrier is blow-dried. That is, the surface of the catalyst carrier is joined to form the first layer of nano metal particles. The cleaning solution may be ionized water or alcohol. The cleaned catalyst carrier can be dried by nitrogen.
步骤5:触媒载体表面再接合多层奈米金属粒子:将表面完成接合有第一层奈米金属粒子的触媒载体,浸泡于含有3~25%十二烷基氨基醇(1,12-dodecaneamino,简称1,12 DDCA)的甲醇溶液中以进行修饰,取出已修饰的接合有第一层奈米金属粒子的触媒载体进行烘干程序,再浸泡于步骤2已制备的水相奈米金属粒子溶液中,以静置1~3小时后,取出已接合有第一层奈米金属粒子的触媒载体并以清洗溶液进行清洗,再将已接合有第一层奈米金属粒子的触媒载体进行吹干,即完成已接合有第一层奈米金属粒子的触媒载体其表面再接合形成有第二层奈米金属粒子。所述步骤5的烘干程序为将接合有第一层奈米金属粒子的触媒载体放置于试管中并置入80℃~90℃烘箱烘干即可。所述清洗溶液可以是离子水或酒精。所述已清洗完成的触媒载体可由氮气进行吹干。Step 5: The surface of the catalyst carrier is then joined with multiple layers of nano metal particles: The surface of the catalyst carrier with the first layer of nano metal particles is immersed in the catalyst carrier containing 3~25% dodecaneamino alcohol (1,12-dodecaneamino). , Abbreviated as 1,12 DDCA) in methanol solution for modification, take out the modified catalyst carrier bonded with the first layer of nano metal particles for drying process, and then soak in the water phase nano metal particles prepared in step 2. After standing for 1 to 3 hours in the solution, take out the catalyst carrier with the first layer of nano metal particles attached and wash it with a cleaning solution, and then blow the catalyst carrier with the first layer of nano metal particles attached Dry, that is, the catalyst carrier with the first layer of nano metal particles is completed, and the surface of the catalyst carrier is joined to form the second layer of nano metal particles. The drying procedure of the step 5 is to place the catalyst carrier with the first layer of nano metal particles in a test tube and put it in an oven at 80°C to 90°C for drying. The cleaning solution may be ionized water or alcohol. The cleaned catalyst carrier can be dried by nitrogen.
另外,本发明可以重复进行步骤5,让已具第二层奈米金属粒子的触媒载体其表面可形成有多层(如第三层、第四层,以此类推)奈米金属粒子;此外,步骤3、步骤5中所述的水相奈米金属粒子溶液可以是相同金属粒子材质或不相同金属粒子材质,使得所述触媒载体其每一层奈米金属粒子的材质可以是相同的、部分相同的或全部不相同的,达到让具第一层奈米金属粒子的触媒载体其表面,可形成有多层单一成份(或多种复合成份)奈米金属粒子。例如:所述触媒载体的第一、二层(或多层)奈米金属粒子的材质皆可以是奈米金粒子;所述触媒载体的第一层奈米金属粒子的材质,皆可以是奈米金粒子、而其中第二层(或其它层)奈米金属粒子的材质,皆可以是奈米白金粒子;所述触媒载体的第一层奈米金属粒子的材质皆,可以是奈米金粒子、而其中第二层奈米金属粒子的材质,可以是奈米白金粒子、且其它层奈米金属粒子的材质,可以是奈米银粒子(或其它材质的奈米金属粒子)。In addition, the present invention can repeat step 5, so that the catalyst carrier that has a second layer of nano metal particles can have multiple layers (such as the third layer, the fourth layer, and so on) formed on the surface of the catalyst carrier; in addition, , The aqueous nano metal particle solution in step 3 and step 5 can be the same metal particle material or different metal particle material, so that the material of each layer of the catalyst carrier can be the same, Some of the same or all of them are different, so that the surface of the catalyst carrier with the first layer of nano-metal particles can be formed with multiple layers of single-component (or multiple-component) nano-metal particles. For example, the material of the first layer and the second layer (or multiple layers) of the catalyst carrier can be nano-gold particles; the material of the first layer of the catalyst carrier can be nano-metal particles. The material of the rice gold particles, and the second layer (or other layer) of the nano metal particles can be nano platinum particles; the material of the first layer of the catalyst carrier can be nano metal particles. Particles, and the material of the second layer of nano metal particles can be nano platinum particles, and the material of other layers of nano metal particles can be nano silver particles (or nano metal particles of other materials).
所述完成步骤5的触媒反应物1,可设置于一放置盘3,所述的放置盘3设有多个等距间隔排列的承置槽31,每一承置槽31其周围设有至少一透孔32,透孔32与承置槽31形成相通;如此,可将多触媒反应物1分别设置于放置盘3的承置槽31,使多个触媒反应物1形成等距间隔排列的形式。The catalyst reactant 1 that has completed step 5 can be set on a placing tray 3, and the placing tray 3 is provided with a plurality of holding grooves 31 arranged at equal intervals, and each holding groove 31 is provided with at least A through hole 32, the through hole 32 is formed in communication with the receiving groove 31; in this way, the multi-catalyst reactant 1 can be respectively arranged in the receiving groove 31 of the placing plate 3, so that the plurality of catalyst reactants 1 are arranged at equal intervals form.
所述放置盘3可设置于触媒催化气相反应系统2所设的反应炉21内,由反应炉21内所设的加热器22,先对触媒反应物1进行加热,当触媒反应物1达到一预设温度时,即可将加热器22关闭;此时,燃料桶23内部燃料(可以是甲醇、乙醇、异丙醇或甲烷等其它燃料),通过燃料管231、雾化器232,并以雾化器232将燃料雾化喷布于反应炉21内,使雾化器232所喷出的燃料可穿过每一个承置槽31所设的透孔32,让燃料可均匀分布于每一个触媒反应物1,使多个触媒反应物1能与燃料,形成具较佳及持续性的热反应。The placing tray 3 can be set in the reaction furnace 21 provided in the catalytic gas phase reaction system 2. The heater 22 provided in the reaction furnace 21 first heats the catalyst reactant 1 and when the catalyst reactant 1 reaches one When the temperature is preset, the heater 22 can be turned off; at this time, the fuel inside the fuel tank 23 (may be other fuels such as methanol, ethanol, isopropanol, or methane) passes through the fuel pipe 231, the atomizer 232, and The atomizer 232 atomizes and sprays the fuel in the reactor 21, so that the fuel sprayed from the atomizer 232 can pass through the through hole 32 of each receiving groove 31, so that the fuel can be evenly distributed in each The catalyst reactant 1 enables a plurality of catalyst reactants 1 to react with the fuel to form a better and continuous thermal reaction.
因此,本发明的技术特征在于,利用含有十二烷基氨基醇(1,12-dodecaneamino,简称1,12 DDCA)的甲醇溶液再对已具第一层奈米金属粒子的触媒载体进行修饰,之后再浸泡于相同或不相同金属材质的水相奈米金属粒子溶液中,使已具第一层奈米金属粒子的触媒载体其表面再接合形成有第二层奈米金属粒子;如此,可重复此步骤,让具第一层奈米金属粒子的触媒载体其表面可形成有多层单一成份(或多层及多种复合成份)奈米金属粒子;达到具多层奈米金属粒子的触媒反应物可以利用粒子之间的界面金属(即担体作用力效应),来提升燃料燃烧反应的催化活性,让触媒反应物能具有更低的起燃温度以及高氧化效率;同时,利用具多种奈米金属粒子的触媒反应物1,能有较佳的热反应触媒性能,达到具多种奈米金属粒子的触媒反应物1,比单一奈米金属粒子的反应物具有更好的热稳定性及热反应效率。Therefore, the technical feature of the present invention is to use a methanol solution containing 1,12-dodecaneamino (1,12 DDCA for short) to modify the catalyst carrier that has the first layer of nano metal particles. Afterwards, it is immersed in an aqueous nano-metal particle solution of the same or different metal materials, so that the surface of the catalyst carrier with the first layer of nano-metal particles is joined to form a second layer of nano-metal particles; Repeat this step so that the catalyst carrier with the first layer of nano metal particles can have multiple layers of single component (or multiple and multiple composite components) nano metal particles formed on the surface; reaching a catalyst with multiple layers of nano metal particles The reactant can use the interface metal between the particles (ie, the supporting force effect) to enhance the catalytic activity of the fuel combustion reaction, so that the catalyst reactant can have a lower ignition temperature and high oxidation efficiency; at the same time, it can use a variety of The catalyst reactant 1 of nano metal particles can have better thermal reaction catalyst performance, and the catalyst reactant 1 with a variety of nano metal particles has better thermal stability than the reactant of single nano metal particles. And thermal reaction efficiency.
显然,所描述的实施例仅仅是本发明的一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative work shall fall within the protection scope of the present invention.
Claims (11)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE112020006680.0T DE112020006680T5 (en) | 2020-04-16 | 2020-04-16 | Process for preparing a catalyst reactant for highly efficient catalysis in a thermal reaction |
| PCT/CN2020/085118 WO2021208013A1 (en) | 2020-04-16 | 2020-04-16 | Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2020/085118 WO2021208013A1 (en) | 2020-04-16 | 2020-04-16 | Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2021208013A1 true WO2021208013A1 (en) | 2021-10-21 |
Family
ID=78084748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/CN2020/085118 Ceased WO2021208013A1 (en) | 2020-04-16 | 2020-04-16 | Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE112020006680T5 (en) |
| WO (1) | WO2021208013A1 (en) |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6413905B1 (en) * | 1998-11-26 | 2002-07-02 | Basf Aktiengesellschaft | Supported catalyst and its use in hydrogenation |
| CN101224430A (en) * | 2008-01-30 | 2008-07-23 | 中国科学院山西煤炭化学研究所 | A kind of hydrophobic organically modified cobalt-based Fischer-Tropsch synthesis catalyst and its preparation and application |
| CN101920201A (en) * | 2009-06-09 | 2010-12-22 | 中国石油化工股份有限公司 | Method for preparing cobalt-based Fischer-Tropsch synthesis catalyst |
| CN103071541A (en) * | 2013-01-18 | 2013-05-01 | 中国科学院广州能源研究所 | Method for preparing supported metal catalyst with high dispersion active center |
| CN104676579A (en) * | 2015-03-09 | 2015-06-03 | 四川能节环保科技有限公司 | High-efficiency energy-saving emission reduction system with clean coal combustion technology |
| CN105268465A (en) * | 2014-07-22 | 2016-01-27 | 华东师范大学 | Silicon oxide-loaded ruthenium catalyst modified or unmodified with organic functional group and containing nickel or no nickel, and preparation method and application thereof |
| US20160076774A1 (en) * | 2014-09-11 | 2016-03-17 | Colorado State University Research Foundation | Side-Feed Forced-Air Biomass Burning Cookstove |
| CN107308951A (en) * | 2016-04-27 | 2017-11-03 | 中国科学技术大学 | Preparation method of the warm catalyst of width for preferential oxidation CO in hydrogen-rich atmosphere and products thereof and application |
-
2020
- 2020-04-16 WO PCT/CN2020/085118 patent/WO2021208013A1/en not_active Ceased
- 2020-04-16 DE DE112020006680.0T patent/DE112020006680T5/en active Pending
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6413905B1 (en) * | 1998-11-26 | 2002-07-02 | Basf Aktiengesellschaft | Supported catalyst and its use in hydrogenation |
| CN101224430A (en) * | 2008-01-30 | 2008-07-23 | 中国科学院山西煤炭化学研究所 | A kind of hydrophobic organically modified cobalt-based Fischer-Tropsch synthesis catalyst and its preparation and application |
| CN101920201A (en) * | 2009-06-09 | 2010-12-22 | 中国石油化工股份有限公司 | Method for preparing cobalt-based Fischer-Tropsch synthesis catalyst |
| CN103071541A (en) * | 2013-01-18 | 2013-05-01 | 中国科学院广州能源研究所 | Method for preparing supported metal catalyst with high dispersion active center |
| CN105268465A (en) * | 2014-07-22 | 2016-01-27 | 华东师范大学 | Silicon oxide-loaded ruthenium catalyst modified or unmodified with organic functional group and containing nickel or no nickel, and preparation method and application thereof |
| US20160076774A1 (en) * | 2014-09-11 | 2016-03-17 | Colorado State University Research Foundation | Side-Feed Forced-Air Biomass Burning Cookstove |
| CN104676579A (en) * | 2015-03-09 | 2015-06-03 | 四川能节环保科技有限公司 | High-efficiency energy-saving emission reduction system with clean coal combustion technology |
| CN107308951A (en) * | 2016-04-27 | 2017-11-03 | 中国科学技术大学 | Preparation method of the warm catalyst of width for preferential oxidation CO in hydrogen-rich atmosphere and products thereof and application |
Also Published As
| Publication number | Publication date |
|---|---|
| DE112020006680T5 (en) | 2023-01-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN108821262A (en) | A method of utilizing semiconductor laser induction polyimide surface carbonization preparation nanometer high-specific surface area carbon particle | |
| CN107597104B (en) | Oxide supported Pt catalyst with core-shell structure and preparation method and application thereof | |
| CN101705613A (en) | Method for preparing flexible air purifying material by low temperature in situ synthesis | |
| CN110102271A (en) | The Multi-hole section and its method, equipment containing nano adsorber administered for VOCs | |
| CN108554174A (en) | A kind of industrial waste gas catalytic treatment equipment and its operating method | |
| WO2021208013A1 (en) | Method for manufacturing catalyst reactant for high-efficiency catalysis in thermal reaction | |
| CN108404666A (en) | A kind of marine diesel tail gas denitrification apparatus | |
| CN107876093A (en) | A kind of method of metal state in alkaline N regulation and control metal-carbide organic framework material | |
| TWI738300B (en) | Method of manufacturing catalyst reactant with high-efficiency thermal reaction catalysis | |
| CN104148091B (en) | Integral automobile tail gas clean-up three-way catalyst and preparation method thereof | |
| CN113522370B (en) | Preparation method of catalytic reactant with high-efficiency catalysis of thermal reaction | |
| CN115254086B (en) | Preparation method of high-efficiency photocatalyst taking fly ash as carrier | |
| CN1504260A (en) | Integral gas combustion catalyst and preparation method thereof | |
| CN103626404A (en) | Method for preparing nano titanium dioxide self-cleaning glass | |
| CN115364886B (en) | Plasma photocatalytic material and application thereof in carbon dioxide cycloaddition reaction | |
| CN114984864B (en) | High-energy-efficiency low-carbon-emission internal electric heating fixed bed hydrogen production reactor | |
| CN104100974A (en) | Low-temperature catalysis type infrared gas heater and catalyst preparation process thereof | |
| CN111099557A (en) | A method for constructing an integrated photocatalytic water splitting system using liquid metal current collectors | |
| CN210945336U (en) | Atomizer | |
| CN208025853U (en) | Gas heater | |
| CN206935115U (en) | A kind of catalyst container and air pollutants arrangement for catalytic purification | |
| CN207762930U (en) | A kind of catalytic combustion device of production of enamel wire exhaust gas | |
| CN115155606B (en) | Bi (Bi) 2 MoO 6 /NiTiO 3 Preparation method and application of heterojunction photocatalytic film material | |
| CN1837029A (en) | Spontaneous recombination system for the conversion and separation of hydrogen from aqueous methanol particles | |
| CN106040233B (en) | A kind of capillary pillar can plasma regenerated catalyst preparation method |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 20930966 Country of ref document: EP Kind code of ref document: A1 |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 20930966 Country of ref document: EP Kind code of ref document: A1 |