WO2022148146A1 - 湿敏多孔陶瓷、雾化芯及其制备方法 - Google Patents

湿敏多孔陶瓷、雾化芯及其制备方法 Download PDF

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WO2022148146A1
WO2022148146A1 PCT/CN2021/131626 CN2021131626W WO2022148146A1 WO 2022148146 A1 WO2022148146 A1 WO 2022148146A1 CN 2021131626 W CN2021131626 W CN 2021131626W WO 2022148146 A1 WO2022148146 A1 WO 2022148146A1
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component
parts
moisture
sensitive porous
porous ceramic
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PCT/CN2021/131626
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English (en)
French (fr)
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林光榕
秦飞
刘卫丽
郑贤彬
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惠州市新泓威科技有限公司
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Publication of WO2022148146A1 publication Critical patent/WO2022148146A1/zh

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    • C04B38/068Carbonaceous materials, e.g. coal, carbon, graphite, hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M11/00Sprayers or atomisers specially adapted for therapeutic purposes
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Definitions

  • the invention belongs to the technical field of humidity-sensitive porous ceramics and atomizing cores manufactured by the humidity-sensitive porous ceramics, and particularly relates to a humidity-sensitive porous ceramics, an atomizing core and a preparation method thereof.
  • the electronic atomizer includes a liquid storage device and an atomizing core.
  • the liquid storage device is filled with the liquid to be atomized.
  • the liquid to be atomized that is, the liquid to be atomized can be smoke liquid or a solution containing drugs.
  • the atomizing core generally includes a guide. Liquid and heating element, conducting liquid to receive, penetrate, and conduct the liquid to be atomized in the liquid storage device, the heating element generates heat after being energized, and the atomizing core is used to heat, evaporate, and atomize the liquid to be atomized into aerosol or steam, Vapor mist for users to inhale and use for health and medical purposes.
  • the atomization core is the key component of the electronic atomizer, and its performance directly determines the atomization effect, heating efficiency and user experience of the electronic atomizer.
  • the atomizing core on the market is usually composed of liquid-conducting cotton plus heating resistance wire, or ceramic liquid-conducting and heating resistance wire.
  • the combination method brings a certain degree of improvement in heat transfer efficiency.
  • the temperature of the atomizing core will rise sharply, resulting in dry burning of the atomizing core, and the atomizing core is easily damaged and burnt. The smell of burnt, causing a bad user experience.
  • the method of preventing dry burning of the existing atomizing core is generally to detect the temperature, and when the temperature rises to a set threshold, the power supply is turned off and the use is stopped. This method of detecting temperature has a certain hysteresis because the temperature rises to a certain degree after the lack of the atomized liquid occurs, and a certain degree of dry burning occurs inevitably.
  • the technical problem to be solved by the present invention is to overcome the problem that the existing atomizing core cannot prevent dry burning in time, and provide a moisture-sensitive porous ceramic, an atomizing core and a preparation method thereof.
  • the technical solution of the present invention is a moisture-sensitive porous ceramic, which is made of a base material, the base material includes A component, B component, C component, a pore-forming agent and a sintering aid, the A group Divided into one or more of SnO 2 , ZnO and TiO 2 , the B component is one or more of LiZnVO 4 , ZnCrVO 4 , V 2 O 5 , Fe 2 O 3 , and the C component is Divided into one or more of Li 2 O, Na 2 O, K 2 O, MgO, CaO, wherein the A component is 1-20 parts, the B component is 1-10 parts, and the C component is 1-20 parts , 1-30 parts of pore-forming agent, 1-10 parts of sintering aid.
  • the A component is 1-10 parts
  • the B component is 1-5 parts
  • the C component is 1-10 parts
  • the pore-forming agent is 1-20 parts
  • the sintering aid is 1-10 parts.
  • the pore-forming agent is at least one of graphite, starch, flour, soybean flour, polystyrene microspheres, polymethyl methacrylate microspheres, carbonates, ammonium salts, sucrose, and fibers.
  • the particle size of the pore-forming agent is 1-200 microns.
  • the sintering aid is at least one of boron oxide, boric acid, oleic acid, stearic acid, sodium silicate, and calcium oxide.
  • the base material further comprises the following components in parts by weight: 1-40 parts of nano-silicon oxide.
  • the nano-silica is nano-silica, and the nano-silica is colloidal nano-silica or powdery nano-silica.
  • the porosity of the moisture-sensitive porous ceramic is 30-70%.
  • Another technical solution of the present invention is an atomizing core, comprising a liquid conducting liquid for conducting the liquid to be atomized and a heating element arranged on the conducting liquid, the conducting liquid is made of the moisture-sensitive porous ceramics to make.
  • Another technical solution of the present invention is, a preparation method of moisture-sensitive porous ceramics, comprising the following steps:
  • component A is SnO 2 , ZnO, and TiO 2 .
  • the B component is one or more of LiZnVO 4 , ZnCrVO 4 , V 2 O 5 , Fe 2 O 3
  • the C component is Li 2 O, Na 2 O, K
  • 2 O, MgO, CaO One or more of 2 O, MgO, CaO;
  • the sintering process includes heating, heat preservation, and cooling to obtain moisture-sensitive porous ceramics.
  • the rotational speed of the ball milling device is set to 150-350 rpm, the ball-milling time is 1-12 h, and the diameter of the abrasive is 1-20 mm.
  • the temperature of baking and drying is 60-120° C.
  • the time of baking and drying is 2-12 hours.
  • the melting point of the paraffin wax is 50-110° C.
  • the weight of the paraffin wax is 10-60% of the weight of the mixed powder.
  • the temperature for removing wax is 400-800° C.
  • the time for removing wax is 2-12 hours.
  • the sintering temperature is 700-1200 °C
  • the heating rate is 1-5 °C/min
  • the sintering holding time is 2-12 h
  • the sintering protective atmosphere is a reducing atmosphere
  • the reducing atmosphere includes Mixing of hydrogen with argon, nitrogen, helium and other gases, where hydrogen accounts for 1-20% of the mixed gas.
  • the present invention utilizes the characteristic that the humidity-sensitive material has different resistance values when the dry humidity of the liquid to be atomized is different, the humidity-sensitive material is added into the ceramic matrix material and the porous ceramic is made into an integrated humidity-sensitive porous ceramic, which is used as the atomizing core
  • the conductive liquid can conduct the liquid to be atomized and has a resistance value that is sensitive to humidity, and its humidity can be measured by detecting its resistance, so that when the liquid to be atomized is lacking in the conductive liquid, its humidity is reduced and can be Quickly detect, so as to reduce the power or turn off the power in time, which can prevent the atomizing core from drying out quickly and without delay.
  • FIG. 1 is a schematic structural diagram of the atomizing core of the present invention.
  • the moisture-sensitive material in the present invention refers to a functional material whose resistance value changes with the humidity of the environment. It is processed by infiltrating substances that are easy to absorb moisture, such as magnesium oxide and chromium oxide, into the electrical insulating material. It can convert changes in humidity into electrical signals through resistance values. Moisture-sensitive materials can realize automatic indication, automatic recording, automatic control and adjustment of humidity.
  • a moisture-sensitive porous ceramic of the present invention is made of a base material, and the base material includes a component A, a component B, a component C, a pore-forming agent and a sintering aid, and the component A is: One or more of SnO 2 , ZnO and TiO 2 , B component is LiZnVO 4 , ZnCrVO 4 , one or more of V 2 O 5 , Fe 2 O 3 , C component is Li 2 O, One or more of Na 2 O, K 2 O, MgO, CaO, wherein the A component is 1-20 parts, the B component is 1-10 parts, the C component is 1-20 parts, and the pore-forming agent is 1- 30 parts, 1-10 parts of sintering aid.
  • the A component is 1-10 parts
  • the B component is 1-5 parts
  • the C component is 1-10 parts
  • the pore-forming agent is 1-20 parts
  • the sintering aid is 1-10 parts.
  • the pore-forming agent is at least one of graphite, starch, flour, soybean flour, polystyrene microspheres, polymethyl methacrylate microspheres, carbonate, ammonium salt, sucrose, and fiber, and the pore-forming agent particles
  • the diameter is 1 to 200 microns.
  • the sintering aid is at least one of boron oxide, boric acid, oleic acid, stearic acid, sodium silicate and calcium oxide.
  • the porosity of moisture-sensitive porous ceramics is 30-70%.
  • the matrix material may also include the following raw material components by weight: 1 to 40 parts of nano-silica, nano-silica is nano-silica, and nano-silica is colloidal nano-silica or powdery nano-silica.
  • Silica After adding the components of nano-silica, a micro-nano composite structure is formed through the curing reaction during the calcination process. Due to its ultra-high specific surface area and a large number of hydroxyl groups on the surface, nano-silica can effectively react with ceramic powder in solid phase. By lowering the sintering temperature, nano-silica can enable the product to maintain high porosity and achieve high strength at the same time. Under the condition of high strength and stable internal structure, this moisture-sensitive porous ceramic is more difficult to be broken, and it is not easy to separate out impurities and precipitate heavy metals during use, which can avoid heavy metals exceeding the standard to the greatest extent.
  • the moisture-sensitive porous ceramics of the present invention can be made into an atomizing core.
  • the atomizing core is used in an electronic atomization device (not shown in the figure).
  • the electronic atomization device includes an atomization component and a battery component, and the battery component is used to control the atomization.
  • the atomization assembly includes a liquid storage device and an atomization core, and the liquid storage device is filled with the liquid to be atomized.
  • the atomizing core of the present invention comprises a conducting liquid for conducting the liquid to be atomized and a heating element arranged on the conducting liquid, wherein the conducting liquid is made of moisture-sensitive porous ceramics.
  • the preparation method of the moisture-sensitive porous ceramics of the present invention comprises the following steps:
  • component A is SnO 2 , ZnO, and TiO 2 .
  • the B component is one or more of LiZnVO 4 , ZnCrVO 4 , V 2 O 5 , Fe 2 O 3
  • the C component is Li 2 O, Na 2 O, K
  • 2 O, MgO, CaO One or more of 2 O, MgO, CaO;
  • the sintering process includes heating, heat preservation, and cooling to obtain moisture-sensitive porous ceramics.
  • step (1) the rotational speed of the ball milling device is set to 150-350 rpm, the ball-milling time is 1-12 h, and the diameter of the abrasive is 1-20 mm.
  • step (2) the temperature for baking and drying is 60-120° C., and the time for baking and drying is 2-12 hours.
  • step (3) the melting point of the paraffin wax is 50-110° C., and the weight of the paraffin wax is 10-60% of the weight of the mixed powder.
  • step (5) the temperature for removing wax is 400-800° C., and the time for removing wax is 2-12 hours.
  • the sintering temperature is 700-1200°C
  • the heating rate is 1-5°C/min
  • the sintering holding time is 2-12h
  • the sintering protective atmosphere is a reducing atmosphere
  • the reducing atmosphere includes hydrogen and argon, Mixing of nitrogen, helium and other gases, in which hydrogen accounts for 1-20% of the mixed gas.
  • the moisture-sensitive porous ceramic of the embodiment of the present invention is made of a base material, the base material includes A component, B component, C component, a pore-forming agent and a sintering aid, and A component includes SnO 2 , ZnO, TiO 2 , B component includes ZnCrVO 4 , V 2 O 5 , C component includes Li 2 O, MgO, CaO, of which A component is 10 parts, B component 5 parts, C component 5 parts, pore-forming agent 20 parts It is 150 micron graphite, and 10 parts of sintering aid is oleic acid.
  • the moisture-sensitive porous ceramic of the embodiment of the present invention is made of a base material, the base material includes A component, B component, C component, a pore-forming agent and a sintering aid, and A component includes SnO 2 , ZnO, TiO 2 , B component includes ZnCrVO 4 , V 2 O 5 , C component includes Li 2 O, MgO, CaO, of which A component is 10 parts, B component 5 parts, C component 5 parts, pore-forming agent 20 parts It is 150 micron graphite, 10 parts of sintering aids are oleic acid, and 20 parts are nano-silica. Nano-silica is silica sol with a particle size of 150 nm, and the amount of nano-silica in the silica sol is calculated as the solid content of silica.
  • the atomizing core of the embodiment of the present invention includes a liquid conducting element 1, a heating element (not shown in the figure), positive and negative electrodes 2 arranged at both ends of the heating element, and a
  • the humidity detection electrode 3, the heating element is arranged inside the liquid conducting liquid 1, the liquid conducting liquid 1 is used to conduct the liquid to be atomized, the liquid conducting liquid 1 is made of the humidity-sensitive porous ceramics described in the previous embodiment, and the liquid to be atomized is from top to bottom. It flows down to the liquid guide 1, and the liquid guide liquid 1 can conduct and penetrate the liquid to be atomized.
  • the conductive liquid 1 includes a humidity-sensitive material.
  • the humidity-sensitive material has certain conductivity and resistance, and its resistance varies with humidity.
  • a humidity detection electrode 3 is connected to the humidity-sensitive material.
  • the humidity detection electrode 3 can detect the conductive liquid 1. humidity inside.
  • the humidity of the liquid guide 1 refers to the relative humidity. When the liquid guide 1 completely absorbs, penetrates, and stores the liquid to be atomized in a maximum amount, its humidity is 100%. When the liquid guide 1 does not absorb the liquid to be atomized, it is completely dry. Its humidity is 0%.
  • the humidity sensor 13 can sense the humidity of the conductive liquid 1 through the change of resistance value.
  • the sintering process includes heating, heat preservation, and cooling.
  • the sintering temperature is 1000°C
  • the heating rate is 5°C/min
  • the sintering holding time is 10h.
  • the protective atmosphere is a reducing atmosphere
  • the reducing atmosphere includes a mixture of hydrogen and argon, wherein hydrogen accounts for 15% of the mixed gas, and finally a moisture-sensitive porous ceramic is obtained.

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Abstract

本发明涉及湿敏多孔陶瓷、雾化芯及其制备方法,湿敏多孔陶瓷由基体材料包括A组分1-20份、B组分1-10份、C组分1-20份、造孔剂1-30份和烧结助剂1-10份制成,A组分为SnO2、ZnO、TiO2,B组分为LiZnVO4、ZnCrVO4,V2O5、Fe2O3,C组分为Li2O、Na2O,K2O,MgO,CaO中的一种或多种;雾化芯包括导液体和发热元件,导液体由湿敏多孔陶瓷制成;制备方法包括:(1)称取A组分、B组分、C组分、造孔剂和烧结助剂,置于球磨装置中混合球磨;(2)烘烤干燥得到混合粉料;(3)将石蜡加热至融化边搅拌边加入混合粉料得到石蜡浆料;(4)将石蜡浆料注入模具中,冷却得到蜡模;(5)放入炉中除蜡得到除蜡样;(6)在保护气氛中进行烧结得到湿敏多孔陶瓷。

Description

湿敏多孔陶瓷、雾化芯及其制备方法 技术领域
本发明属于湿敏多孔陶瓷、湿敏多孔瓷制造的雾化芯技术领域,特别涉及一种湿敏多孔陶瓷、雾化芯及其制备方法。
背景技术
电子雾化器包括储液装置和雾化芯,储液装置中灌装有待雾化液,待雾化液即待雾化的液体可以是烟液或含有药物的溶液,雾化芯一般包括导液体和发热元件,导液体接收、渗透、传导储液装置中的待雾化液,发热元件通电后发热,雾化芯用于将待雾化液进行加热、蒸发、雾化成气溶胶或蒸汽、汽雾,以便用户吸食,用于健康医疗之用途。雾化芯是电子雾化器的关键部件,其性能优劣直接决定了电子雾化器的雾化效果,加热效率及使用体验。
目前市场上的雾化芯通常由导液棉加发热电阻丝、或陶瓷导液体和加热电阻丝组成,电阻丝与陶瓷导液体的结合方式有植入式、印刷式、贴片式等,不同的结合方式在传热效率上带来了一定程度的提升。现有的雾化芯,在待雾化液即将用完或传导不顺畅时,雾化芯的温度就会急剧升高,导致雾化芯发生干烧,雾化芯容易被烧损和产生烧焦的味道,给用户造成不良的使用体验。现有雾化芯的防止干烧的方法一般是检测温度,在温度升高到设定的阈值时,则关断供电电源停止使用。此种检测温度的方法由于是在待雾化液缺乏发生之后温度上升到一定程度才被检测到,具有一定的滞后性,不免还是有一定程度的干烧发生。
技术问题
本发明所要解决的技术问题是克服现有雾化芯防干烧不及时的问题,提供一种湿敏多孔陶瓷、雾化芯及其制备方法。
技术解决方案
本发明的技术解决方案是,一种湿敏多孔陶瓷,由基体材料制成,所述基体材料包括A组分、B组分、C组分、造孔剂和烧结助剂,所述A组分为SnO 2、ZnO、TiO 2中的一种或多种,所述B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,所述C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种,其中A组分为1-20份,B组分1-10份,C组分1-20份,造孔剂1-30份,烧结助剂1-10份。
优选地,所述A组分为1-10份,B组分1-5份,C组分1-10份,造孔剂1-20份,烧结助剂1-10份。
优选地,所述造孔剂为石墨、淀粉、面粉、豆粉、聚苯乙烯微球、聚甲基丙烯酸甲酯微球、碳酸盐、铵盐、蔗糖、纤维中的至少一种,所述造孔剂粒径为1~200微米。
优选地,所述烧结助剂为氧化硼、硼酸、油酸、硬脂酸、硅酸钠、氧化钙中的至少一种。
优选地,所述基体材料按重量份还包括如下组分:纳米氧化硅1~40份。
优选地,所述纳米氧化硅为纳米二氧化硅,所述纳米二氧化硅为胶体状的纳米二氧化硅或粉体状的纳米二氧化硅。
优选地,所述湿敏多孔陶瓷的孔隙率是30~70%。
本发明的另一技术解决方案是,一种雾化芯,包括用于传导待雾化液的导液体和设于导液体上的发热元件,所述导液体由所述的湿敏多孔陶瓷制成。
本发明的又一技术解决方案是,一种湿敏多孔陶瓷的制备方法,包括以下步骤:
(1)按照配方称取A组分、B组分、C组分、造孔剂、烧结助剂,置于球磨装置中混合球磨;所述A组分为SnO 2、ZnO、TiO 2中的一种或多种,所述B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,所述C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种;
(2)将球磨后的混合料烘烤干燥,得到混合粉料;
(3)将石蜡加热至融化状态,边搅拌边加入所述混合粉料,加入完毕后继续搅拌1~8h,得到石蜡浆料;
(4)将所述石蜡浆料注入预先准备的模具中,冷却成型,脱模后得到蜡模;
(5)将所述蜡模放入炉中进行预加热进行除蜡,得到除蜡样;
(6)将所述除蜡样放入炉中并在保护气氛中进行烧结,烧结过程包括升温、保温、降温,得到湿敏多孔陶瓷。
优选地,所述步骤(1)中,球磨装置的转速设为150~350rpm,球磨时间为1~12h,磨料直径为1~20mm。
优选地,所述步骤(2)中,烘烤干燥的温度为60~120℃,烘烤干燥的时间为2~12h。
优选地,所述步骤(3)中,所述石蜡的熔点为50~110℃,所述石蜡的重量为所述混合粉料重量的10~60%。
优选地,所述步骤(5)中,除蜡的温度为400~800℃,除蜡的时间为2~12h。
优选地,所述步骤(6)中,烧结的温度为700~1200℃,升温速度1~5℃/min,烧结的保温时间为2~12h;烧结保护气氛为还原性气氛,还原性气氛包括氢气与氩气、氮气、氦气等气体的混合,其中氢气在混合气体中占比1-20%。
有益效果
本发明利用湿敏材料在待雾化液的干湿度不同时具有不同电阻阻值的特性,将湿敏材料加入陶瓷基体材料中和多孔陶瓷做成一体式的湿敏多孔陶瓷,作为雾化芯的导液体,该导液体可传导待雾化液并具有对湿度敏感的电阻阻值,通过检测其电阻可测定其湿度,这样在导液体内缺乏待雾化液时其湿度减小并可被迅速检测到,从而及时减小功率或关停电源,可迅速、无延时地防止雾化芯发生干烧。
附图说明
图1是本发明的雾化芯的结构示意图。
本发明的最佳实施方式
本发明中的湿敏材料是指材料的电阻值随所处环境的湿度变化而变化的功能材料,它是在电绝缘物质中渗入容易吸潮的物质,如氧化镁、氧化铬等加工而成。它能将湿度的变化通过电阻值转换成电的信号。湿敏材料可以实现湿度的自动指示、自动记录、自动控制与调节。
本发明的一种湿敏多孔陶瓷,一种湿敏多孔陶瓷,由基体材料制成,基体材料包括A组分、B组分、C组分、造孔剂和烧结助剂,A组分为SnO 2、ZnO、TiO 2中的一种或多种,B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种,其中A组分为1-20份,B组分1-10份,C组分1-20份,造孔剂1-30份,烧结助剂1-10份。优选的,A组分为1-10份,B组分1-5份,C组分1-10份,造孔剂1-20份,烧结助剂1-10份。
其中,造孔剂为石墨、淀粉、面粉、豆粉、聚苯乙烯微球、聚甲基丙烯酸甲酯微球、碳酸盐、铵盐、蔗糖、纤维中的至少一种,造孔剂粒径为1~200微米。烧结助剂为氧化硼、硼酸、油酸、硬脂酸、硅酸钠、氧化钙中的至少一种。湿敏多孔陶瓷的孔隙率是30~70%。
另外,基体材料按重量份还可以包括如下原料组分:纳米氧化硅1~40份,纳米氧化硅为纳米二氧化硅,纳米二氧化硅为胶体状的纳米二氧化硅或粉体状的纳米二氧化硅。加入纳米氧化硅的组分后,在煅烧过程中通过固化反应形成微纳米复合结构,纳米氧化硅由于其超高比表面积,且表面含有大量的羟基,在与陶瓷粉体固相反应时能有效降低烧结温度,纳米氧化硅可以使产品同时保持高孔隙率和实现高强度。在高强度、内部结构稳定的条件下,此湿敏多孔陶瓷更不易碎裂,且在使用过程中不易分离出杂质和析出重金属,可最大限度地避免重金属超标。
本发明的湿敏多孔陶瓷可制成一种雾化芯,雾化芯用于电子雾化设备(图中未示),电子雾化设备包括雾化组件和电池组件,电池组件用于控制雾化组件及提供电源给雾化组件。雾化组件包括储液装置和雾化芯,储液装置中灌装有待雾化液,待雾化液即待雾化的液体可以是烟液或含有药物的溶液。本发明的雾化芯,包括用于传导待雾化液的导液体和设于导液体上的发热元件,其中的导液体由湿敏多孔陶瓷制成。
本发明湿敏多孔陶瓷的制备方法,包括以下步骤:
(1)按照配方称取A组分、B组分、C组分、造孔剂、烧结助剂,置于球磨装置中混合球磨;所述A组分为SnO 2、ZnO、TiO 2中的一种或多种,所述B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,所述C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种;
(2)将球磨后的混合料烘烤干燥,得到混合粉料;
(3)将石蜡加热至融化状态,边搅拌边加入所述混合粉料,加入完毕后继续搅拌1~8h,得到石蜡浆料;
(4)将所述石蜡浆料注入预先准备的模具中,冷却成型,脱模后得到蜡模;
(5)将所述蜡模放入炉中进行预加热进行除蜡,得到除蜡样;
(6)将所述除蜡样放入炉中并在保护气氛中进行烧结,烧结过程包括升温、保温、降温,得到湿敏多孔陶瓷。
其中,步骤(1)中,球磨装置的转速设为150~350rpm,球磨时间为1~12h,磨料直径为1~20mm。步骤(2)中,烘烤干燥的温度为60~120℃,烘烤干燥的时间为2~12h。步骤(3)中,石蜡的熔点为50~110℃,石蜡的重量为混合粉料重量的10~60%。步骤(5)中,除蜡的温度为400~800℃,除蜡的时间为2~12h。步骤(6)中,烧结的温度为700~1200℃,升温速度1~5℃/min,烧结的保温时间为2~12h;烧结保护气氛为还原性气氛,还原性气氛包括氢气与氩气、氮气、氦气等气体的混合,其中氢气在混合气体中占比1-20%。
本发明的实施方式
下面将通过具体实施例对本发明进行详细说明。
实施例一
本发明实施例的湿敏多孔陶瓷,由基体材料制成,基体材料包括A组分、B组分、C组分、造孔剂和烧结助剂,A组分包括SnO 2、ZnO、TiO 2,B组分包括ZnCrVO 4,V 2O 5,C组分包括Li 2O、MgO,CaO,其中A组分为10份,B组分5份,C组分5份,造孔剂20份为150微米的石墨,烧结助剂10份为油酸。
实施例二
本发明实施例的湿敏多孔陶瓷,由基体材料制成,基体材料包括A组分、B组分、C组分、造孔剂和烧结助剂,A组分包括SnO 2、ZnO、TiO 2,B组分包括ZnCrVO 4,V 2O 5,C组分包括Li 2O、MgO,CaO,其中A组分为10份,B组分5份,C组分5份,造孔剂20份为150微米的石墨,烧结助剂10份为油酸,20份的纳米二氧化硅。纳米二氧化硅为粒径150nm的硅溶胶,硅溶胶的纳米二氧化硅的量以其中固体份二氧化硅计。
实施例三
本发明实施例的雾化芯,如图1所示,该雾化芯包括导液体1、发热元件(图中未示)、设于发热元件两端的正负电极2、与湿敏材料连接的湿度检测电极3,发热元件设于导液体1的内部,导液体1用于传导待雾化液,导液体1由前面实施例所述的湿敏多孔陶瓷制成,待雾化液自上而下流动到导液体1,导液液体1可传导、渗透待雾化液。导液体1内包括湿敏材料,湿敏材料具有一定的导电性和电阻,其电阻随湿度不同而变化,与湿敏材料连接设有湿度检测电极3,通过湿度检测电极3可检测导液体1内的湿度。
导液体1的湿度是指相对湿度,当导液体1完全吸收、渗透、及最大量地贮存待雾化液时,其湿度为100%,导液体1没有吸收待雾化液即完全干燥时,其湿度为0%。湿敏元件13可通过阻值变化感应导液体1的湿度。
实施例四
本发明实施例的湿敏多孔陶瓷的制备方法,包括以下步骤:
(1)按照配方称取A组分包括SnO 2、ZnO、TiO 2,B组分包括ZnCrVO 4,V 2O 5,C组分包括Li 2O、MgO,CaO,其中A组分为10份,B组分5份,C组分5份,造孔剂20份为150微米的石墨,烧结助剂10份为油酸,置于球磨装置中混合球磨,球磨装置的转速设为300rpm,球磨时间为8h,磨料直径为20mm;
(2)将球磨后的混合料烘烤干燥,得到混合粉料,烘烤干燥的温度为90℃,烘烤干燥的时间为10h。
(3)将石蜡加热至65℃至融化状态,边搅拌边加入混合粉料,加入完毕后继续搅拌8h,得到石蜡浆料;石蜡的熔点为60℃,石蜡的重量为混合粉料重量的50%;
(4)将石蜡浆料注入预先准备的模具中,冷却成型,脱模后得到蜡模;
(5)将蜡模放入炉中进行预加热进行除蜡,除蜡的温度为800℃,除蜡的时间为12h,得到除蜡样;
(6)将除蜡样放入炉中并在保护气氛中进行烧结,烧结过程包括升温、保温、降温,烧结的温度为1000℃,升温速度5℃/min,烧结的保温时间为10h,烧结保护气氛为还原性气氛,还原性气氛包括氢气与氩气的混合,其中氢气在混合气体中占比15%,最后得到湿敏多孔陶瓷。
工业实用性
以上所述仅为本发明的较佳实施例,凡依本发明权利要求范围所做的均等变化与修饰,皆应属本发明权利要求的涵盖范围。

Claims (14)

  1. 一种湿敏多孔陶瓷,其特征在于,由基体材料制成,所述基体材料包括A组分、B组分、C组分、造孔剂和烧结助剂,所述A组分为SnO 2、ZnO、TiO 2中的一种或多种,所述B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,所述C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种,其中A组分为1-20份,B组分1-10份,C组分1-20份,造孔剂1-30份,烧结助剂1-10份。
  2. 根据权利要求1所述的湿敏多孔陶瓷,其特征在于,所述A组分为1-10份,B组分1-5份,C组分1-10份,造孔剂1-20份,烧结助剂1-10份。
  3. 根据权利要求1所述的湿敏多孔陶瓷,其特征在于,所述造孔剂为石墨、淀粉、面粉、豆粉、聚苯乙烯微球、聚甲基丙烯酸甲酯微球、碳酸盐、铵盐、蔗糖、纤维中的至少一种,所述造孔剂粒径为1~200微米。
  4. 根据权利要求1所述的湿敏多孔陶瓷,其特征在于,所述烧结助剂为氧化硼、硼酸、油酸、硬脂酸、硅酸钠、氧化钙中的至少一种。
  5. 根据权利要求1所述的湿敏多孔陶瓷,其特征在于,所述基体材料按重量份还包括如下组分:纳米氧化硅1~40份。
  6. 根据权利要求5所述的湿敏多孔陶瓷,其特征在于,所述纳米氧化硅为纳米二氧化硅,所述纳米二氧化硅为胶体状的纳米二氧化硅或粉体状的纳米二氧化硅。
  7. 根据权利要求1所述的湿敏多孔陶瓷,其特征在于,所述湿敏多孔陶瓷的孔隙率是30~70%。
  8. 一种雾化芯,其特征在于,包括用于传导待雾化液的导液体和设于导液体上的发热元件,所述导液体由权利要求1~7任一项所述的湿敏多孔陶瓷制成。
  9. 一种湿敏多孔陶瓷的制备方法,其特征在于,包括以下步骤:
    (1)按照配方称取A组分、B组分、C组分、造孔剂、烧结助剂,置于球磨装置中混合球磨;所述A组分为SnO 2、ZnO、TiO 2中的一种或多种,所述B组分为LiZnVO 4、ZnCrVO 4,V 2O 5、Fe 2O 3中的一种或多种,所述C组分为Li 2O、Na 2O,K 2O,MgO,CaO中的一种或多种;
    (2)将球磨后的混合料烘烤干燥,得到混合粉料;
    (3)将石蜡加热至融化状态,边搅拌边加入所述混合粉料,加入完毕后继续搅拌1~8h,得到石蜡浆料;
    (4)将所述石蜡浆料注入预先准备的模具中,冷却成型,脱模后得到蜡模;
    (5)将所述蜡模放入炉中进行预加热进行除蜡,得到除蜡样;
    (6)将所述除蜡样放入炉中并在保护气氛中进行烧结,烧结过程包括升温、保温、降温,得到湿敏多孔陶瓷。
  10. 根据权利要求9所述的湿敏多孔陶瓷的制备方法,其特征在于,所述步骤(1)中,球磨装置的转速设为150~350rpm,球磨时间为1~12h,磨料直径为1~20mm。
  11. 根据权利要求9所述的湿敏多孔陶瓷的制备方法,其特征在于,所述步骤(2)中,烘烤干燥的温度为60~120℃,烘烤干燥的时间为2~12h。
  12. 根据权利要求9所述的湿敏多孔陶瓷的制备方法,其特征在于,所述步骤(3)中,所述石蜡的熔点为50~110℃,所述石蜡的重量为所述混合粉料重量的10~60%。
  13. 根据权利要求9所述的湿敏多孔陶瓷的制备方法,其特征在于,所述步骤(5)中,除蜡的温度为400~800℃,除蜡的时间为2~12h。
  14. 根据权利要求9所述的湿敏多孔陶瓷的制备方法,其特征在于,所述步骤(6)中,烧结的温度为700~1200℃,升温速度1~5℃/min,烧结的保温时间为2~12h;烧结保护气氛为还原性气氛,还原性气氛包括氢气与氩气、氮气、氦气等气体的混合,其中氢气在混合气体中占比1-20%。
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Publication number Priority date Publication date Assignee Title
CN112841754A (zh) * 2021-01-08 2021-05-28 深圳市康泓威科技有限公司 具有湿敏元件的电子雾化设备及其防干烧控制方法
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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63194307A (ja) * 1987-02-09 1988-08-11 株式会社村田製作所 感湿セラミツク
CN1765822A (zh) * 2005-09-08 2006-05-03 广州大学 二氧化锡-钒酸锌锂复合棒状晶粒湿敏陶瓷材料及制备方法
CN103880410A (zh) * 2014-02-14 2014-06-25 江西理工大学 熔盐法合成ZnO-Cr2O3-Fe2O3系湿敏陶瓷烧结粉体方法
CN110713379A (zh) * 2019-12-02 2020-01-21 湖南福美来电子陶瓷有限公司 一种多孔陶瓷雾化芯及其制备方法
CN111205104A (zh) * 2020-01-14 2020-05-29 东莞市陶陶新材料科技有限公司 电子烟用多孔陶瓷及其制备方法
CN111792922A (zh) * 2020-07-10 2020-10-20 湖南云天雾化科技有限公司 一种高还原多孔陶瓷雾化芯及其制备方法
CN112811925A (zh) * 2021-01-08 2021-05-18 惠州市新泓威科技有限公司 湿敏多孔陶瓷、雾化芯及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1983001339A1 (en) * 1981-09-30 1983-04-14 Uchikawa, Fusaoki Humidity sensor
JPH05264494A (ja) * 1992-03-18 1993-10-12 Nippon Oil & Fats Co Ltd 感湿素子
CN1101453A (zh) * 1993-10-08 1995-04-12 北京新奇材料研究所 一种陶瓷湿敏元件的制作方法
CN103653261B (zh) * 2013-12-13 2016-03-23 上海烟草集团有限责任公司 一种智能电子烟
CN105753509B (zh) * 2016-02-01 2018-08-31 浙江大学 一种湿敏陶瓷及其制备方法和应用

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63194307A (ja) * 1987-02-09 1988-08-11 株式会社村田製作所 感湿セラミツク
CN1765822A (zh) * 2005-09-08 2006-05-03 广州大学 二氧化锡-钒酸锌锂复合棒状晶粒湿敏陶瓷材料及制备方法
CN103880410A (zh) * 2014-02-14 2014-06-25 江西理工大学 熔盐法合成ZnO-Cr2O3-Fe2O3系湿敏陶瓷烧结粉体方法
CN110713379A (zh) * 2019-12-02 2020-01-21 湖南福美来电子陶瓷有限公司 一种多孔陶瓷雾化芯及其制备方法
CN111205104A (zh) * 2020-01-14 2020-05-29 东莞市陶陶新材料科技有限公司 电子烟用多孔陶瓷及其制备方法
CN111792922A (zh) * 2020-07-10 2020-10-20 湖南云天雾化科技有限公司 一种高还原多孔陶瓷雾化芯及其制备方法
CN112811925A (zh) * 2021-01-08 2021-05-18 惠州市新泓威科技有限公司 湿敏多孔陶瓷、雾化芯及其制备方法

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