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CN116784529A - Liquid storage part, atomizer, aerosol generating device and liquid storage part preparation method - Google Patents

Liquid storage part, atomizer, aerosol generating device and liquid storage part preparation method Download PDF

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Publication number
CN116784529A
CN116784529A CN202310798063.5A CN202310798063A CN116784529A CN 116784529 A CN116784529 A CN 116784529A CN 202310798063 A CN202310798063 A CN 202310798063A CN 116784529 A CN116784529 A CN 116784529A
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liquid storage
liquid
atomizer
aerogel
porous
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邱伟华
杨臣
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Zhuoyue International Holdings Ltd
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Zhuoyue International Holdings Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C69/00Combinations of shaping techniques not provided for in a single one of main groups B29C39/00 - B29C67/00, e.g. associations of moulding and joining techniques; Apparatus therefore
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24FSMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/40Constructional details, e.g. connection of cartridges and battery parts
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24FSMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/40Constructional details, e.g. connection of cartridges and battery parts
    • A24F40/42Cartridges or containers for inhalable precursors
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24FSMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/70Manufacture
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • C08G73/1007Preparatory processes from tetracarboxylic acids or derivatives and diamines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1039Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors comprising halogen-containing substituents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1046Polyimides containing oxygen in the form of ether bonds in the main chain
    • C08G73/105Polyimides containing oxygen in the form of ether bonds in the main chain with oxygen only in the diamino moiety
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1067Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
    • C08G73/1071Wholly aromatic polyimides containing oxygen in the form of ether bonds in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0066Use of inorganic compounding ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/28Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2201/00Foams characterised by the foaming process
    • C08J2201/04Foams characterised by the foaming process characterised by the elimination of a liquid or solid component, e.g. precipitation, leaching out, evaporation
    • C08J2201/048Elimination of a frozen liquid phase
    • C08J2201/0482Elimination of a frozen liquid phase the liquid phase being organic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2205/00Foams characterised by their properties
    • C08J2205/04Foams characterised by their properties characterised by the foam pores
    • C08J2205/044Micropores, i.e. average diameter being between 0,1 micrometer and 0,1 millimeter
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2379/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2361/00 - C08J2377/00
    • C08J2379/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
    • C08J2379/08Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

The application provides a liquid storage piece, an atomizer, an aerosol generating device and a liquid storage piece preparation method, wherein an ether ammonolysis is carried out in a mixed solvent of dioxane (Diox) and Tertiary Butyl Alcohol (TBA) through a fluorine-containing aromatic dianhydride monomer and a diamine monomerThe polyamide acid (PAA) solution is formed by reaction, ammonium chloride particles are taken as pore-forming agents, the polyamide acid (PAA) solution added with the ammonium chloride particles is injected into a mould to be frozen, and the PAA-NH is obtained by freeze drying 4 After the Cl aerogel is subjected to thermal imidization treatment, the porous polyimide aerogel can be prepared. The preparation method of the liquid storage piece provided by the embodiment of the application can reasonably regulate and control the pore size of the porous polyimide aerogel according to the use requirement, has the advantages of short preparation flow and simple process, can reduce the instability of the product caused by unstable factors, and can reduce the manufacturing cost, energy consumption and pollutant emission of the liquid storage piece.

Description

储液件、雾化器、气溶胶发生装置及储液件制备方法Liquid storage part, atomizer, aerosol generating device and preparation method of liquid storage part

技术领域Technical field

本发明属于雾化技术领域,特别地,涉及一种储液件、雾化器、气溶胶发生装置及储液件制备方法。The invention belongs to the field of atomization technology, and in particular, relates to a liquid storage part, an atomizer, an aerosol generating device and a method for preparing a liquid storage part.

背景技术Background technique

气溶胶发生装置通常包括雾化器以及与雾化器电性连接的电源装置,雾化器能够在电源装置的电驱动作用下,将存储于雾化器内的气溶胶形成基质加热并雾化形成气溶胶。当前,雾化器上一般设置有储液腔,并在储液腔中设置储液件,储液件通常由纤维棉制成。由于纤维棉的结构比较柔软蓬松,在储液件受到的挤压作用力较大时易出现雾化液泄漏,而在储液件受到的挤压作用力较小时容易导致雾化液残留量较多。The aerosol generating device usually includes an atomizer and a power supply device electrically connected to the atomizer. The atomizer can heat and atomize the aerosol-forming matrix stored in the atomizer under the electric driving action of the power supply device. Aerosols are formed. At present, atomizers are generally provided with a liquid storage chamber, and a liquid storage part is provided in the liquid storage chamber. The liquid storage part is usually made of fiber cotton. Since the structure of fiber cotton is relatively soft and fluffy, atomized liquid leakage is likely to occur when the liquid storage part is subjected to a large squeezing force, and when the liquid storage part is subjected to a small squeezing force, it is easy to cause a large amount of residual atomized liquid. many.

发明内容Contents of the invention

基于现有技术中存在的上述问题,本发明实施例的目的之一在于提供一种储液件,以解决现有技术中存在的储液件漏液或储液件残留较多雾化液的问题。Based on the above-mentioned problems existing in the prior art, one of the purposes of the embodiments of the present invention is to provide a liquid storage member to solve the problems in the prior art of leakage of liquid storage member or residual atomized liquid in the liquid storage member. question.

为实现上述目的,本发明采用的技术方案是:提供一种储液件,用于雾化器,所述雾化器包括雾化弹主体和用于将雾化液雾化形成气溶胶的雾化芯,所述雾化芯设置于所述雾化弹主体中,所述雾化弹主体内部设有储液腔,所述储液件设置于所述储液腔中;所述储液件为多孔气凝胶,以使所述储液件可用于储存雾化液,且所述储液件可将储存的雾化液传输至所述雾化芯。In order to achieve the above object, the technical solution adopted by the present invention is to provide a liquid storage member for use in an atomizer. The atomizer includes an atomization bomb body and a mist for atomizing the atomized liquid to form an aerosol. atomization core, the atomization core is arranged in the main body of the atomization bomb, the main body of the atomization bomb is provided with a liquid storage chamber, and the liquid storage member is arranged in the liquid storage cavity; the liquid storage member It is a porous aerogel, so that the liquid storage member can be used to store atomized liquid, and the liquid storage member can transfer the stored atomized liquid to the atomization core.

可选地,所述多孔气凝胶为采用聚酰亚胺制成的多孔气凝胶基体。Optionally, the porous airgel is a porous airgel matrix made of polyimide.

可选地,所述多孔气凝胶的储液量为800~1000mg/g。Optionally, the porous aerogel has a liquid storage capacity of 800 to 1000 mg/g.

如权利要求1所述的储液件,其特征在于,所述多孔气凝胶的孔径为0.1~100μm。The liquid storage member according to claim 1, wherein the porous aerogel has a pore diameter of 0.1 to 100 μm.

可选地,所述多孔气凝胶呈柱状,所述多孔气凝胶沿轴向贯穿设置有套孔,所述雾化芯位于所述套孔中。Optionally, the porous aerogel is columnar, the porous aerogel is provided with a set of holes through the axial direction, and the atomization core is located in the set of holes.

可选地,所述多孔气凝胶的外周面与所述储液腔的内侧面抵触,所述套孔的孔壁与所述雾化芯的外周面抵触。Optionally, the outer peripheral surface of the porous aerogel conflicts with the inner surface of the liquid storage chamber, and the hole wall of the sleeve hole conflicts with the outer peripheral surface of the atomization core.

基于现有技术中存在的上述问题,本发明实施例的目的之二在于提供一种具有上述任一方案提供的储液件的雾化器。Based on the above-mentioned problems existing in the prior art, the second object of the embodiments of the present invention is to provide an atomizer having a liquid storage member provided by any of the above-mentioned solutions.

为实现上述目的,本发明采用的技术方案是:提供一种雾化器,包括上述任一方案提供的所述储液件。In order to achieve the above object, the technical solution adopted by the present invention is to provide an atomizer including the liquid storage member provided by any of the above solutions.

可选地,所述雾化芯包括设于所述雾化弹主体中的雾化支架、设于所述雾化支架中的发热体和用于向所述发热体传输雾化液的导液件,所述导液件设于所述雾化支架中,所述雾化支架上设有用于向所述导液件传输雾化液的导液口,所述多孔气凝胶遮蔽所述导液口。Optionally, the atomization core includes an atomization bracket provided in the atomization bomb body, a heating body provided in the atomization bracket, and a liquid guide for transmitting atomized liquid to the heating body. The liquid guide member is provided in the atomization bracket, and the atomization bracket is provided with a liquid guide port for transmitting atomized liquid to the liquid guide member, and the porous aerogel shields the guide liquid port.

可选地,所述雾化弹主体包括设有吸气口的雾化壳体、设于所述雾化壳体的底部敞口上的底座和设于所述雾化壳体中的通气管,所述雾化芯支撑于所述底座上,所述通气管连接所述雾化芯与所述吸气口,所述雾化壳体内部于所述雾化芯及所属通气管之外的部分界定出所述储液腔,所述雾化芯上设有连通所述储液腔的导液口,所述多孔气凝胶封闭所述导液口。Optionally, the atomization bomb body includes an atomization housing provided with an air suction port, a base provided on the bottom opening of the atomization housing, and a breather tube provided in the atomization housing, The atomizing core is supported on the base, the vent pipe connects the atomizing core and the suction port, and the inside of the atomizing shell is outside the atomizing core and the associated vent pipe. The liquid storage chamber is defined, the atomization core is provided with a liquid conduction port connected to the liquid storage chamber, and the porous aerogel seals the liquid conduction port.

基于现有技术中存在的上述问题,本发明实施例的目的之三在于提供一种具有上述任一方案提供的储液件或雾化器的气溶胶发生装置。Based on the above problems existing in the prior art, the third object of the embodiments of the present invention is to provide an aerosol generating device having a liquid storage member or an atomizer provided by any of the above solutions.

为实现上述目的,本发明采用的技术方案是:提供一种气溶胶发生装置,包括上述任一方案提供的所述储液件或所述雾化器。In order to achieve the above object, the technical solution adopted by the present invention is to provide an aerosol generating device, including the liquid storage member or the atomizer provided by any of the above solutions.

本发明实施例中的上述一个或多个技术方案,与现有技术相比,至少具有如下有益效果之一:Compared with the existing technology, one or more of the above technical solutions in the embodiments of the present invention have at least one of the following beneficial effects:

本发明实施例中的储液件、雾化器及气溶胶发生装置,采用多孔气凝胶作为储存雾化液的储液件,由于多孔气凝胶的结构紧密性良好,可防止储液件受到挤压作用而发生严重变形,从而克服现有技术中采用纤维棉作为储液件,在储液件受到的挤压作用力较小时易出现雾化液泄漏,而在储液件受到的挤压作用力较大时容易导致雾化液残留量较多的缺陷。并且,多孔气凝胶容易实现表面官能团修饰,拓展表面极性调控的范围与空间,能极大的保留表面亲油基团,采用多孔气凝胶作为储液件,有利于雾化液的快速传输。此外,多孔气凝胶的软硬可根据实际使用需要进行调控,多孔气凝胶不掉粉,不会释放原料小颗粒,避免对人体呼吸道造成损害。The liquid storage part, atomizer and aerosol generating device in the embodiment of the present invention use porous aerogel as the liquid storage part to store the atomized liquid. Since the porous aerogel has good structural tightness, it can prevent the liquid storage part from Severe deformation occurs due to squeezing, thereby overcoming the existing technology that uses fiber cotton as a liquid storage part. When the squeezing force on the liquid storage part is small, atomized liquid leakage is prone to occur, and when the liquid storage part is squeezed under When the pressure force is large, it is easy to cause the defect of large residual amount of atomized liquid. In addition, porous aerogels can easily modify surface functional groups, expand the range and space of surface polarity control, and can greatly retain surface lipophilic groups. Using porous aerogels as liquid storage parts is conducive to rapid atomization of liquids. transmission. In addition, the softness and hardness of the porous aerogel can be adjusted according to actual use needs. The porous aerogel does not lose powder and does not release small particles of raw materials to avoid damage to the human respiratory tract.

基于现有技术中存在的上述问题,本发明实施例的目的之四在于提供一种储液件制备方法。Based on the above-mentioned problems existing in the prior art, the fourth object of the embodiments of the present invention is to provide a method for preparing a liquid storage member.

为实现上述目的,本发明采用的技术方案是:提供一种储液件制备方法,包括如下步骤:In order to achieve the above object, the technical solution adopted by the present invention is to provide a method for preparing a liquid storage member, which includes the following steps:

步骤S01:将二氧六环与叔丁醇溶液进行混合,得到混合溶剂;Step S01: Mix dioxane and tert-butyl alcohol solution to obtain a mixed solvent;

步骤S02:向所述混合溶剂中添加含氟芳香二酐单体和二胺单体,通过醚的氨解反应,得到聚酰胺酸溶液;Step S02: Add fluorine-containing aromatic dianhydride monomer and diamine monomer to the mixed solvent, and obtain a polyamic acid solution through the ammonolysis reaction of ether;

步骤S03:向所述聚酰胺酸溶液中添加氯化铵颗粒,搅拌均匀,得到PAA-NH4Cl悬浊液Step S03: Add ammonium chloride particles to the polyamic acid solution and stir evenly to obtain a PAA-NH 4 Cl suspension.

步骤S04:将所述PAA-NH4Cl悬浊液注入模具中进行冷冻,通过冷冻干燥处理,得到PAA-NH4Cl气凝胶;Step S04: Inject the PAA-NH 4 Cl suspension into a mold for freezing, and obtain PAA-NH 4 Cl aerogel through freeze-drying;

步骤S05:将脱模后的所述PAA-NH4Cl气凝胶进行加热,通过热亚胺化处理,制备得到可作为储液件的多孔聚酰亚胺气凝胶。Step S05: Heat the demolded PAA-NH 4 Cl aerogel, and prepare a porous polyimide aerogel that can be used as a liquid storage member through thermal imidization treatment.

可选地,在所述步骤S01中,所述叔丁醇溶液占所述混合溶剂的体积比重在0~30%。Optionally, in step S01, the volume proportion of the tert-butyl alcohol solution in the mixed solvent is 0 to 30%.

可选地,在所述步骤S04中,冷冻干燥处理的冷冻速率为5~10℃/min。Optionally, in step S04, the freezing rate of the freeze-drying process is 5-10°C/min.

可选地,在所述步骤S03中,所述氯化铵颗粒的粒径在60~140μm。Optionally, in step S03, the particle size of the ammonium chloride particles is between 60 and 140 μm.

可选地,在所述步骤S03中,添加所述氯化铵颗粒的质量为1~10g。Optionally, in step S03, the mass of the ammonium chloride particles added is 1 to 10 g.

可选地,在所述步骤S05中,热亚胺化处理的升温速率为1~5℃/min。Optionally, in the step S05, the temperature rise rate of the thermal imidization treatment is 1 to 5°C/min.

可选地,在所述步骤S05中,热亚胺化处理的温度为240~270℃,热亚胺化处理的时间为0.5~2h。Optionally, in step S05, the temperature of the thermal imidization treatment is 240 to 270°C, and the time of the thermal imidization treatment is 0.5 to 2 hours.

可选地,在所述步骤S02中,添加的含氟芳香二酐单体和二胺单体为等摩尔比。Optionally, in step S02, the added fluorine-containing aromatic dianhydride monomer and diamine monomer are in an equal molar ratio.

可选地,在所述步骤S05中,反应生成的所述聚酰胺酸溶液占含氟芳香二酐单体和二胺单体的质量百分比为10~20%。Optionally, in step S05, the mass percentage of the polyamic acid solution generated by the reaction in the fluorinated aromatic dianhydride monomer and diamine monomer is 10 to 20%.

本发明实施例中的上述一个或多个技术方案,与现有技术相比,至少具有如下有益效果之一:Compared with the existing technology, one or more of the above technical solutions in the embodiments of the present invention have at least one of the following beneficial effects:

本发明实施例中的储液件制备方法,通过含氟芳香二酐单体和二胺单体,在二氧六环(Diox)和叔丁醇(TBA)的混合溶剂中进行醚的氨解反应形成聚酰胺酸(PAA)溶液,以氯化铵颗粒为造孔剂,并将添加有氯化铵颗粒的聚酰胺酸(PAA)溶液将注入模具进行冷冻,冷冻干燥处理得到的PAA-NH4Cl气凝胶经热亚胺化处理后,可制备得到可作为储液件的多孔聚酰亚胺气凝胶。本发明实施例提供的储液件制备方法,可根据使用需要对多孔聚酰亚胺气凝胶的孔径大小进行合理调控,制备流程短,工艺简单,不仅可降低不稳定因素导致的产品不稳定性,而且能够降低储液件的制作成本、能耗以及污染物排放。The liquid storage member preparation method in the embodiment of the present invention uses fluorine-containing aromatic dianhydride monomer and diamine monomer to perform ammonolysis of ether in a mixed solvent of dioxane (Diox) and tert-butyl alcohol (TBA). The reaction forms a polyamic acid (PAA) solution, using ammonium chloride particles as a pore-forming agent, and the polyamic acid (PAA) solution with added ammonium chloride particles is injected into the mold for freezing, and the resulting PAA-NH is freeze-dried. After thermal imidization treatment of 4 Cl aerogel, a porous polyimide aerogel that can be used as a liquid storage component can be prepared. The liquid storage member preparation method provided by the embodiment of the present invention can reasonably regulate the pore size of the porous polyimide aerogel according to the needs of use. The preparation process is short and the process is simple. It can not only reduce product instability caused by unstable factors It is flexible and can reduce the production cost, energy consumption and pollutant emissions of liquid storage parts.

附图说明Description of the drawings

为了更清楚地说明本发明实施例中的技术方案,下面将对实施例或现有技术描述中所需要使用的附图作简单地介绍,显而易见地,下面描述中的附图仅仅是本发明的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动性的前提下,还可以根据这些附图获得其他的附图。In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed to be used in the description of the embodiments or prior art will be briefly introduced below. Obviously, the drawings in the following description are only illustrative of the present invention. For some embodiments, for those of ordinary skill in the art, other drawings can be obtained based on these drawings without exerting creative efforts.

图1为本发明实施例提供的储液件的立体结构示意图;Figure 1 is a schematic three-dimensional structural diagram of a liquid storage member provided by an embodiment of the present invention;

图2为本发明实施例提供的雾化器的立体结构示意图;Figure 2 is a schematic three-dimensional structural diagram of an atomizer provided by an embodiment of the present invention;

图3为本发明实施例提供的雾化器与储液件装配图;Figure 3 is an assembly diagram of the atomizer and liquid storage parts provided by the embodiment of the present invention;

图4为本发明实施例提供的雾化器的剖视结构示意图;Figure 4 is a schematic cross-sectional structural view of an atomizer provided by an embodiment of the present invention;

图5为本发明实施例提供的雾化芯的爆炸图;Figure 5 is an exploded view of the atomizing core provided by the embodiment of the present invention;

图6为本发明实施例提供的雾化器的爆炸图。Figure 6 is an exploded view of the atomizer provided by the embodiment of the present invention.

其中,图中各附图标记:Among them, each figure in the figure is marked with:

1-多孔气凝胶;11-套孔;1-porous airgel; 11-holes;

2-雾化器;21-雾化弹主体;211-雾化壳体;212-底座;213-通气管;22-雾化芯;221-雾化支架;222-发热体;223-导液件;2-Atomizer; 21-Atomizer bomb body; 211-Atomizer shell; 212-Base; 213-Breath tube; 22-Atomizer core; 221-Atomizer bracket; 222-Heating element; 223-Liquid conductor pieces;

3-吸气口;4-导液口;5-储液腔;3-suction port; 4-liquid guide port; 5-liquid storage chamber;

6-吸嘴;7-密封塞。6-Suction nozzle; 7-Sealing plug.

具体实施方式Detailed ways

为了使本发明所要解决的技术问题、技术方案及有益效果更加清楚明白,以下结合附图及实施例,对本发明进行进一步详细说明。应当理解,此处所描述的具体实施例仅仅用以解释本发明,并不用于限定本发明。In order to make the technical problems, technical solutions and beneficial effects to be solved by the present invention clearer, the present invention will be further described in detail below with reference to the drawings and embodiments. It should be understood that the specific embodiments described here are only used to explain the present invention and are not intended to limit the present invention.

需要说明的是,当元件被称为“连接于”或“设置于”另一个元件,它可以直接在另一个元件上或者间接在该另一个元件上。当一个元件被称为是“连接于”另一个元件,它可以是直接连接到另一个元件或间接连接至该另一个元件上。此外,术语“第一”、“第二”仅用于描述目的,而不能理解为指示或暗示相对重要性或者隐含指明所指示的技术特征的数量。由此,限定有“第一”、“第二”的特征可以明示或者隐含地包括一个或者更多个该特征。在本发明的描述中,“多个”的含义是两个或两个以上,除非另有明确具体的限定。“多个”的含义是一个或一个以上,除非另有明确具体的限定。It should be noted that when an element is referred to as being "connected to" or "disposed on" another element, it can be directly on the other element or indirectly on the other element. When an element is referred to as being "connected to" another element, it can be directly connected to the other element or indirectly connected to the other element. In addition, the terms “first” and “second” are used for descriptive purposes only and cannot be understood as indicating or implying relative importance or implicitly indicating the quantity of indicated technical features. Therefore, features defined as "first" and "second" may explicitly or implicitly include one or more of these features. In the description of the present invention, "plurality" means two or more than two, unless otherwise explicitly and specifically limited. "Plural" means one or more than one, unless otherwise expressly and specifically limited.

在本发明的描述中,需要理解的是,术语“中心”、“长度”、“宽度”、“厚度”、“上”、“下”、“前”、“后”、“左”、“右”、“竖直”、“水平”、“顶”、“底”、“内”、“外”等指示的方位或位置关系为基于附图所示的方位或位置关系,仅是为了便于描述本发明和简化描述,而不是指示或暗示所指的装置或元件必须具有特定的方位、以特定的方位构造和操作,因此不能理解为对本发明的限制。In the description of the present invention, it should be understood that the terms "center", "length", "width", "thickness", "upper", "lower", "front", "back", "left", " The directions or positional relationships indicated by "right", "vertical", "horizontal", "top", "bottom", "inside", "outside", etc. are based on the directions or positional relationships shown in the drawings and are for convenience only. The invention is described and the description is simplified without indicating or implying that the device or element referred to must have a particular orientation, be constructed and operate in a particular orientation, and therefore is not to be construed as a limitation of the invention.

在本发明的描述中,需要说明的是,除非另有明确的规定和限定,术语“安装”、“相连”、“连接”应做广义理解,例如,可以是固定连接,也可以是可拆卸连接,或一体地连接;可以是机械连接,也可以是电性连接;可以是直接相连,也可以通过中间媒介间接相连,可以是两个元件内部的连通或两个元件的相互作用关系。对于本领域的普通技术人员而言,可以根据具体情况理解上述术语在本发明中的具体含义。In the description of the present invention, it should be noted that, unless otherwise clearly stated and limited, the terms "installation", "connection" and "connection" should be understood in a broad sense. For example, it can be a fixed connection or a detachable connection. Connection, or integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium; it can be an internal connection between two elements or an interaction between two elements. For those of ordinary skill in the art, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

在整个说明书中参考“一个实施例”或“实施例”意味着结合实施例描述的特定特征,结构或特性包括在本申请的至少一个实施例中。因此,“在一个实施例中”、“在一些实施例中”或“在其中一些实施例中”的短语出现在整个说明书的各个地方,并非所有的指代都是相同的实施例。此外,在一个或多个实施例中,可以以任何合适的方式组合特定的特征,结构或特性。Reference throughout this specification to "one embodiment" or "an embodiment" means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment of the present application. Thus, the phrases "in one embodiment," "in some embodiments," or "in some of these embodiments" appear in various places throughout this specification, and not all are referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.

请一并参阅图1、图3和图4,现对本发明实施例提供的储液件进行说明。本发明实施例提供的储液件用于雾化器2,雾化器2包括雾化弹主体21和用于将雾化液雾化形成气溶胶的雾化芯22,雾化芯22设置于雾化弹主体21中,雾化弹主体21内部设有储液腔5,储液件设置于储液腔5中。储液件为可以吸附、储存及传输雾化液的多孔气凝胶1,且储液件可将储存的雾化液传输至雾化芯22,雾化芯22在通电后产生热量,将雾化液加热并雾化形成气溶胶。Please refer to Figure 1, Figure 3 and Figure 4 together to describe the liquid storage member provided by the embodiment of the present invention. The liquid storage member provided by the embodiment of the present invention is used in the atomizer 2. The atomizer 2 includes an atomization bomb body 21 and an atomization core 22 for atomizing the atomization liquid to form an aerosol. The atomization core 22 is disposed on In the atomizer bomb main body 21, a liquid storage chamber 5 is provided inside the atomizer bomb main body 21, and the liquid storage member is arranged in the liquid storage chamber 5. The liquid storage part is a porous aerogel 1 that can absorb, store and transmit atomized liquid, and the liquid storage part can transmit the stored atomized liquid to the atomizing core 22. The atomizing core 22 generates heat after being powered on, and the mist is transferred to the atomizing core 22. The liquid is heated and atomized to form an aerosol.

本发明实施例提供的储液件,与现有技术相比,采用多孔气凝胶1作为储存雾化液的储液件,由于多孔气凝胶1的结构紧密性良好,可防止储液件受到挤压作用而发生严重变形,从而克服现有技术中采用纤维棉作为储液件,在储液件受到的挤压作用力较小时易出现雾化液泄漏,而在储液件受到的挤压作用力较大时容易导致雾化液残留量较多的缺陷。并且,多孔气凝胶1容易实现表面官能团修饰,拓展表面极性调控的范围与空间,能极大的保留表面亲液基团,采用多孔气凝胶1作为储液件,有利于雾化液的快速传输。此外,多孔气凝胶1的软硬可根据实际使用需要进行调控,多孔气凝胶1不掉粉,不会释放原料小颗粒,避免对人体呼吸道造成损害。Compared with the existing technology, the liquid storage member provided by the embodiment of the present invention uses porous aerogel 1 as the liquid storage member for storing atomized liquid. Due to the good structural tightness of the porous airgel 1, it can prevent the liquid storage member from Severe deformation occurs due to squeezing, thereby overcoming the existing technology that uses fiber cotton as a liquid storage part. When the squeezing force on the liquid storage part is small, atomized liquid leakage is prone to occur, and when the liquid storage part is squeezed under When the pressure force is large, it is easy to cause the defect of large residual amount of atomized liquid. In addition, porous aerogel 1 can easily modify surface functional groups, expand the range and space of surface polarity control, and can greatly retain surface lyophilic groups. Using porous aerogel 1 as a liquid storage component is beneficial to atomizing liquid of fast transfer. In addition, the softness and hardness of the porous aerogel 1 can be adjusted according to actual use needs. The porous aerogel 1 does not lose powder and does not release small particles of raw materials to avoid damage to the human respiratory tract.

在其中一些实施例中,多孔气凝胶1为采用聚酰亚胺制成的多孔气凝胶基体。由于采用聚酰亚胺制成的多孔气凝胶基体通过模具成型,可以做复杂的机构,形状、尺寸和公差均可控制。采用聚酰亚胺制成的多孔气凝胶基体容易实现表面官能团修饰,拓展表面极性调控的范围与空间,一方面表面官能团可以设计,另一方面制备温度在200~300℃,能极大的保留表面亲液基团。采用聚酰亚胺制成的多孔气凝胶基体可以实现表面官能团修饰,当具有丰富的表面官能团时,雾化芯22的发热体222在于雾化液接触的过程中,会有金属离子析出,而多孔聚酰亚胺表面丰富的官能团能有效的捕捉金属离子,降低重金属离子在气溶胶内的释放。采用聚酰亚胺制成的多孔气凝胶基体,储液性能可调,且储液性能更佳,多孔聚酰亚胺的储液量可以达到800~1000mg/g,大于多孔陶瓷的储液量(600~800mg/g)。采用聚酰亚胺制成的多孔气凝胶基体,孔径可实现0.1至100微米调控,不仅适配水果味雾化液,更适配粘度大的雾化液。采用聚酰亚胺制成的多孔气凝胶基体,内部具有纳米多孔结构,纳米多孔结构中的微孔可小于等于2nm,使得纳米多孔结构中的微孔可进行锁液,纳米多孔结构中的孔径为2~50nm的介孔具有良好的锁液性能),纳米多孔结构中的孔径大于50nm的大孔具有良好的导液性能,而且纳米多孔结构的孔径大小可调,可设计与探寻到导液与锁液的平衡点,协调解决漏液与残液问题。采用聚酰亚胺制成的多孔气凝胶基体,解决传统储液棉材质因雾化液媒介与接触的塑胶件发生粘连问题,提高化学安全性与产品稳定性。采用聚酰亚胺制成的多孔气凝胶基体,力学性能可调(软硬调控),做硬的优点在于储液件装配至雾化器2时,结构不易坍塌,不掉粉,完整度高,不易将纤维分散于雾化液中并随抽吸进入人体;做软可以制备成弹性且结构完整,可提高装配贴合度,提高产品稳定性。采用聚酰亚胺制成的多孔气凝胶基体,不掉粉,不涉及原料小颗粒的释放,避免对人体呼吸道损害。一般而言多孔陶瓷是由颗粒状的陶瓷粉体通过玻璃粉作为粘结剂构建而成,所以在抽吸过程中,气溶胶里会有陶瓷粉体小颗粒释放,对人体呼吸道有害。In some embodiments, the porous airgel 1 is a porous airgel matrix made of polyimide. Since the porous airgel matrix made of polyimide is molded through a mold, complex mechanisms can be made, and the shape, size and tolerance can be controlled. The porous airgel matrix made of polyimide can easily be modified with surface functional groups, expanding the range and space of surface polarity control. On the one hand, the surface functional groups can be designed, and on the other hand, the preparation temperature is 200 to 300°C, which can greatly retain surface lyophilic groups. The porous airgel matrix made of polyimide can achieve surface functional group modification. When it has abundant surface functional groups, metal ions will precipitate during the contact between the heating element 222 of the atomizing core 22 and the atomizing liquid. The rich functional groups on the surface of porous polyimide can effectively capture metal ions and reduce the release of heavy metal ions in aerosols. The porous airgel matrix made of polyimide has adjustable liquid storage performance and better liquid storage performance. The liquid storage capacity of porous polyimide can reach 800~1000mg/g, which is larger than that of porous ceramics. Amount (600~800mg/g). The porous airgel matrix is made of polyimide, and the pore size can be adjusted from 0.1 to 100 microns. It is not only suitable for fruit-flavored atomization liquids, but also atomization liquids with high viscosity. The porous airgel matrix made of polyimide has a nanoporous structure inside. The micropores in the nanoporous structure can be less than or equal to 2nm, so that the micropores in the nanoporous structure can lock liquid. Mesopores with a pore diameter of 2 to 50 nm have good liquid-locking properties), and macropores with a pore diameter greater than 50 nm in the nanoporous structure have good liquid conductivity. Moreover, the pore size of the nanoporous structure is adjustable, and the conductivity can be designed and explored. The balance point between liquid and liquid locking can coordinately solve the problems of leakage and residual liquid. The porous airgel matrix made of polyimide solves the problem of adhesion of traditional liquid storage cotton materials to plastic parts in contact with the atomized liquid medium, and improves chemical safety and product stability. The porous aerogel matrix made of polyimide has adjustable mechanical properties (soft and hard control). The advantage of being hard is that when the liquid storage part is assembled to the atomizer 2, the structure is not easy to collapse, the powder does not fall off, and the integrity is high. High, it is not easy for fibers to disperse in the atomized liquid and enter the human body with suction; making it soft can be made elastic and structurally complete, which can improve assembly fit and product stability. The porous airgel matrix made of polyimide does not shed powder and does not involve the release of small particles of raw materials, thus avoiding damage to the human respiratory tract. Generally speaking, porous ceramics are made of granular ceramic powder with glass powder as a binder. Therefore, during the suction process, small particles of ceramic powder are released in the aerosol, which is harmful to the human respiratory tract.

在其中一些实施例中,多孔气凝胶1的孔径为0.1~100μm,采用聚酰亚胺制成的多孔气凝胶基体,多孔气凝胶基体内部的纳米多孔结构中的微孔孔径可在0.1~100μm之间进行调控。例如,在纳米多孔结构中的微孔孔径处于0.1~50μm时,多孔气凝胶基体具有良好的锁液性能,可防止漏液;而在纳米多孔结构中的微孔孔径处于50~100μm时,聚酰亚胺具有良好的导液性能。此外,聚酰亚胺内部的纳米多孔结构中的微孔孔径可在0.1~100μm之间进行调控,易实现对气溶胶细腻程度和口感的调控。In some embodiments, the pore diameter of the porous airgel 1 is 0.1 to 100 μm, and a porous airgel matrix made of polyimide is used. The micropore diameter in the nanoporous structure inside the porous airgel matrix can be Control between 0.1~100μm. For example, when the micropore diameter in the nanoporous structure is between 0.1 and 50 μm, the porous airgel matrix has good liquid-locking properties and can prevent liquid leakage; while when the micropore diameter in the nanoporous structure is between 50 and 100 μm, Polyimide has good liquid conductivity properties. In addition, the diameter of the micropores in the nanoporous structure inside the polyimide can be adjusted between 0.1 and 100 μm, making it easy to control the fineness and taste of the aerosol.

请结合参阅图1、图2和图6,在其中一些实施例中,多孔气凝胶1呈柱状,多孔气凝胶1沿轴向贯穿设置有套孔11,雾化芯22位于套孔11中。在多孔气凝胶1套装于雾化芯22上时,多孔气凝胶1可遮蔽雾化芯22上的导液口4,使得储液腔5与导液口4不能直接连通,防止储液腔5中的雾化液直接通过导液口4进入雾化芯22。可以理解地,多孔气凝胶1的外廓可以呈圆柱状、椭圆柱状或棱柱状等,并且多孔气凝胶1的形状大小与储液腔5的形状大小相适配。具体地,请结合参阅图2、图5和图6,在其中一些实施例中,雾化芯22包括设于雾化弹主体21中的雾化支架221、设于雾化支架221中的发热体222和用于向发热体222传输雾化液的导液件223,导液件223设于雾化支架221中,雾化支架221上设有用于向导液件223传输雾化液的导液口4,多孔气凝胶1遮蔽导液口4,使得储液腔5与导液口4不能直接连通,有效防止储液腔5中的雾化液直接通过导液口4进入雾化芯22。需要说明的是,导液件223可以是但不限于导液棉、多孔陶瓷或采用聚酰亚胺制成的多孔体,发热体222可以是但不限于网状发热件、螺旋发热丝、发热片或发热膜。Please refer to Figure 1, Figure 2 and Figure 6 in combination. In some embodiments, the porous aerogel 1 is columnar, the porous aerogel 1 is provided with a set of holes 11 along the axial direction, and the atomizing core 22 is located in the set of holes 11. middle. When the porous airgel 1 is placed on the atomizing core 22, the porous aerogel 1 can cover the liquid guide port 4 on the atomizer core 22, so that the liquid storage chamber 5 and the liquid guide port 4 cannot be directly connected to prevent liquid storage. The atomized liquid in the cavity 5 directly enters the atomizing core 22 through the liquid guide port 4 . It can be understood that the outer outline of the porous airgel 1 can be cylindrical, elliptical columnar or prism-shaped, etc., and the shape and size of the porous airgel 1 is adapted to the shape and size of the liquid storage chamber 5 . Specifically, please refer to Figure 2, Figure 5 and Figure 6. In some embodiments, the atomization core 22 includes an atomization bracket 221 provided in the atomization bomb body 21, and a heating element provided in the atomization bracket 221. body 222 and a liquid guide 223 for transmitting atomized liquid to the heating element 222. The liquid guide 223 is provided in the atomization bracket 221. The atomization bracket 221 is provided with a liquid guide for transmitting atomized liquid to the liquid guide 223. Port 4, the porous airgel 1 covers the liquid guide port 4, so that the liquid storage chamber 5 and the liquid guide port 4 cannot be directly connected, effectively preventing the atomized liquid in the liquid storage chamber 5 from directly entering the atomization core 22 through the liquid guide port 4. . It should be noted that the liquid-conducting member 223 may be, but is not limited to, liquid-conducting cotton, porous ceramics, or a porous body made of polyimide, and the heating element 222 may be, but is not limited to, a mesh heating member, a spiral heating wire, or a heating element. sheet or heating film.

请结合参阅图3,在其中一些实施例中,多孔气凝胶1的外周面与储液腔5的内侧面抵触,套孔11的孔壁与雾化芯22的外周面抵触,以平衡多孔气凝胶1储液及导液能力,保证雾化液能够稳定均匀地传输至导液口4,又可以减缓雾化液经由导液口4进入雾化芯22中的流速,达到良好的防漏液的效果。Please refer to FIG. 3 . In some embodiments, the outer peripheral surface of the porous airgel 1 conflicts with the inner surface of the liquid storage chamber 5 , and the hole wall of the sleeve hole 11 conflicts with the outer peripheral surface of the atomization core 22 to balance the porous airgel 1 . The liquid storage and liquid conduction capabilities of the airgel 1 ensure that the atomized liquid can be transmitted stably and evenly to the liquid conduction port 4, and can also slow down the flow rate of the atomized liquid into the atomization core 22 through the liquid conduction port 4, thereby achieving good prevention. Leakage effect.

请结合参阅图2、图3和图6,本发明实施例还提供一种雾化器2,雾化器2包括上述任一实施例提供的雾化芯22。因雾化器2具有上述任一实施例提供的雾化芯22的全部技术特征,故其具有雾化芯22相同的技术效果。Please refer to Figure 2, Figure 3 and Figure 6 in conjunction. An embodiment of the present invention also provides an atomizer 2. The atomizer 2 includes the atomizer core 22 provided in any of the above embodiments. Since the atomizer 2 has all the technical features of the atomizer core 22 provided in any of the above embodiments, it has the same technical effects as the atomizer core 22 .

请结合参阅图1、图5和图6,在其中一些实施例中,雾化弹主体21包括设有吸气口3的雾化壳体211、设于雾化壳体211的底部敞口上的底座212和设于雾化壳体211中的通气管213,雾化芯22支撑于底座212上,通气管213连接雾化芯22与吸气口3,雾化壳体211内部于雾化芯22及所属通气管213之外的部分界定出储液腔5,雾化芯22上设有连通储液腔5的导液口4,多孔气凝胶1设于储液腔5中并封闭导液口4。雾化器2工作时,多孔气凝胶1中储存的雾化液经由导液口4传输至雾化芯22,雾化芯22通电后产生的热量可将雾化液加热雾化形成气溶胶,气溶胶通过通气管213引出至吸气口3,用户便可通过吸气口3抽吸到气溶胶。进一步地,为了方便用户抽吸气溶胶,在雾化壳体211上还设有与吸气口3连通的吸嘴6。吸嘴6中设置有密封塞7,在雾化器2未使用时,可通过密封塞7封闭吸嘴6,可达到防尘防漏液的效果。Please refer to Figure 1, Figure 5 and Figure 6 in conjunction. In some embodiments, the atomization bomb body 21 includes an atomization shell 211 provided with an air inlet 3, and an atomization shell 211 provided on the bottom opening of the atomization shell 211. The base 212 and the breather tube 213 located in the atomization housing 211. The atomization core 22 is supported on the base 212. The breather tube 213 connects the atomization core 22 and the suction port 3. The inside of the atomization housing 211 is in the atomization core. 22 and the part outside the associated breather tube 213 defines a liquid storage chamber 5. The atomizing core 22 is provided with a liquid guide port 4 connected to the liquid storage chamber 5. The porous aerogel 1 is located in the liquid storage chamber 5 and seals the guide port. Liquid port 4. When the atomizer 2 is working, the atomized liquid stored in the porous aerogel 1 is transmitted to the atomizing core 22 through the liquid guide port 4. The heat generated by the atomizing core 22 after being powered on can heat and atomize the atomized liquid to form an aerosol. , the aerosol is led to the suction port 3 through the ventilation tube 213, and the user can inhale the aerosol through the suction port 3. Furthermore, in order to facilitate the user to inhale the aerosol, the atomization housing 211 is also provided with a suction nozzle 6 connected with the suction port 3 . The suction nozzle 6 is provided with a sealing plug 7. When the atomizer 2 is not in use, the suction nozzle 6 can be closed by the sealing plug 7, thereby achieving the effect of preventing dust and liquid leakage.

本发明实施例还提供一种气溶胶发生装置,气溶胶发生装置包括上述任一实施例提供的雾化芯22或上述任一实施例提供的雾化器2。因气溶胶发生装置具有上述任一实施例提供的雾化芯22或雾化器2的全部技术特征,故其具有雾化芯22相同的技术效果。An embodiment of the present invention also provides an aerosol generating device. The aerosol generating device includes the atomizing core 22 provided in any of the above embodiments or the atomizer 2 provided in any of the above embodiments. Since the aerosol generating device has all the technical features of the atomizing core 22 or the atomizer 2 provided in any of the above embodiments, it has the same technical effects as the atomizing core 22 .

本发明实施例还提供一种可制备上述储液件的储液件制备方法,本发明实施例中的储液件制备方法包括如下步骤:Embodiments of the present invention also provide a liquid storage part preparation method that can prepare the above-mentioned liquid storage part. The liquid storage part preparation method in the embodiment of the present invention includes the following steps:

步骤S01:将二氧六环与叔丁醇溶液进行混合,得到混合溶剂;Step S01: Mix dioxane and tert-butyl alcohol solution to obtain a mixed solvent;

步骤S02:向混合溶剂中添加含氟芳香二酐单体和二胺单体,通过醚的氨解反应,得到聚酰胺酸溶液;Step S02: Add fluorine-containing aromatic dianhydride monomer and diamine monomer to the mixed solvent, and obtain a polyamic acid solution through the ammonolysis reaction of ether;

步骤S03:向聚酰胺酸溶液中添加氯化铵颗粒,搅拌均匀,得到PAA-NH4Cl悬浊液Step S03: Add ammonium chloride particles to the polyamic acid solution and stir evenly to obtain a PAA-NH 4 Cl suspension.

步骤S04:将PAA-NH4Cl悬浊液注入模具中进行冷冻,通过冷冻干燥处理,得到PAA-NH4Cl气凝胶;Step S04: Inject the PAA-NH 4 Cl suspension into the mold for freezing, and obtain PAA-NH 4 Cl aerogel through freeze-drying;

步骤S05:将脱模后的PAA-NH4Cl气凝胶进行加热,通过热亚胺化处理,得到可作为储液件的多孔聚酰亚胺气凝胶。Step S05: Heat the demolded PAA-NH 4 Cl aerogel and perform thermal imidization treatment to obtain a porous polyimide aerogel that can be used as a liquid storage member.

本发明实施例提供的储液件制备方法,与现有技术相比,通过含氟芳香二酐单体和二胺单体,在二氧六环(Diox)和叔丁醇(TBA)的混合溶剂中进行醚的氨解反应形成聚酰胺酸(PAA)溶液,以氯化铵颗粒为造孔剂,并将添加有氯化铵颗粒的聚酰胺酸(PAA)溶液将注入模具进行冷冻,冷冻干燥处理得到的PAA-NH4Cl气凝胶经热亚胺化处理后,可制备得到多孔聚酰亚胺气凝胶。本发明实施例提供的储液件制备方法,可根据使用需要对多孔聚酰亚胺气凝胶的孔径大小进行合理调控,制备流程短,工艺简单,不仅可降低不稳定因素导致的产品不稳定性,而且能够降低储液件的制作成本、能耗以及污染物排放。本发明实施例提供的储液件制备方法,通过引入氯化铵造孔剂,能够抑制气凝胶在热亚胺化过程中的体积收缩。本发明实施例提供的储液件制备方法,通过冷冻干燥处理过程时形成冰晶结构,可去除溶剂形成聚酰胺酸气凝胶。本发明实施例提供的储液件制备方法,通过热亚胺化过程完成了羧基和亚胺的脱水缩合反应,减少了气凝胶中疏液基团的数量,并使得氯化铵充分受热分解,达到去除氯化铵的目的。Compared with the prior art, the liquid storage member preparation method provided by the embodiment of the present invention uses a fluorine-containing aromatic dianhydride monomer and a diamine monomer, and mixes dioxane (Diox) and tert-butyl alcohol (TBA). The ammonolysis reaction of ether is carried out in the solvent to form a polyamic acid (PAA) solution. Ammonium chloride particles are used as pore-forming agents, and the polyamic acid (PAA) solution with added ammonium chloride particles is injected into the mold for freezing. After the PAA-NH 4 Cl aerogel obtained by drying is thermally imidized, a porous polyimide aerogel can be prepared. The liquid storage member preparation method provided by the embodiment of the present invention can reasonably regulate the pore size of the porous polyimide aerogel according to the needs of use. The preparation process is short and the process is simple. It can not only reduce product instability caused by unstable factors It is flexible and can reduce the production cost, energy consumption and pollutant emissions of liquid storage parts. The liquid storage member preparation method provided by the embodiment of the present invention can suppress the volume shrinkage of the airgel during the thermal imidization process by introducing ammonium chloride pore-forming agent. In the liquid storage component preparation method provided by the embodiment of the present invention, an ice crystal structure is formed during the freeze-drying process, and the solvent can be removed to form a polyamic acid aerogel. The liquid storage member preparation method provided by the embodiment of the present invention completes the dehydration condensation reaction of carboxyl groups and imines through the thermal imidization process, reduces the number of lyophobic groups in the airgel, and allows ammonium chloride to be fully thermally decomposed , to achieve the purpose of removing ammonium chloride.

具体的,在步骤S01中,叔丁醇(TBA)溶液占混合溶剂的体积比重在0~30%。由表1中的测试数据可知,叔丁醇(TBA)溶液占混合溶剂的体积比重在0~30%,有助于对聚酰亚胺气凝胶进行造孔,并兼顾多孔聚酰亚胺气凝胶的高比表面积、形状完整性与结构强度。当叔丁醇溶液占混合溶剂的体积比重大于30%时,虽然能够增大多孔聚酰亚胺气凝胶的比表面积,但多孔聚酰亚胺气凝胶的结构强度显著降低。Specifically, in step S01, the volume proportion of the tert-butyl alcohol (TBA) solution in the mixed solvent is 0-30%. From the test data in Table 1, it can be seen that the volume proportion of tert-butyl alcohol (TBA) solution in the mixed solvent is 0 to 30%, which is helpful to create pores in the polyimide aerogel and takes into account the porous polyimide. The high specific surface area, shape integrity and structural strength of aerogels. When the volume proportion of the tert-butyl alcohol solution in the mixed solvent is greater than 30%, although the specific surface area of the porous polyimide aerogel can be increased, the structural strength of the porous polyimide aerogel is significantly reduced.

具体的,在步骤S04中,冷冻干燥处理的冷冻速率为5~10℃/min,可以获得形状与结构完整的柱状多孔聚酰亚胺气凝胶。在冷冻干燥处理的冷冻速率大于10℃/min或者小于5℃/min时,制备得到的多孔聚酰亚胺气凝胶容易出现大小不等的裂纹以及在柱状中心区产生凹陷等问题。Specifically, in step S04, the freezing rate of the freeze-drying process is 5-10°C/min, and a columnar porous polyimide aerogel with complete shape and structure can be obtained. When the freezing rate of the freeze-drying process is greater than 10°C/min or less than 5°C/min, the prepared porous polyimide aerogel is prone to problems such as cracks of varying sizes and depressions in the columnar central area.

具体的,在步骤S03中,氯化铵颗粒的粒径在60~140μm,可以获得均匀性强的PAA-NH4Cl浆料。由表2中的测试数据可知,氯化铵颗粒的粒径在60~140μm,有利于维持多孔聚酰亚胺气凝胶的结构完整性。Specifically, in step S03, the particle size of the ammonium chloride particles is between 60 and 140 μm, and a PAA-NH 4 Cl slurry with strong uniformity can be obtained. It can be seen from the test data in Table 2 that the particle size of ammonium chloride particles is between 60 and 140 μm, which is beneficial to maintaining the structural integrity of porous polyimide aerogels.

具体的,在步骤S03中,添加氯化铵颗粒的质量为1~10g,可以获得形状与结构完整的柱状多孔聚酰亚胺气凝胶。虽然随着氯化铵添加量的增加,有利于提高多孔聚酰亚胺气凝胶的储液量。然而,当氯化铵的投入量超过10g时,多孔聚酰亚胺气凝胶的结构完整性与力学强度容易受到破坏,不利于多孔聚酰亚胺气凝胶在雾化器2中的安装,降低储液件的使用寿命。由于氯化铵的投入量过大,氯化铵颗粒造孔剂团聚越严重,降低了PAA-NH4Cl浆料的流动性与均匀性,进而导致多孔聚酰亚胺气凝胶的结构出现不完整的缺陷。Specifically, in step S03, the mass of ammonium chloride particles added is 1 to 10 g, and a columnar porous polyimide aerogel with complete shape and structure can be obtained. Although increasing the amount of ammonium chloride added is beneficial to increasing the liquid storage capacity of porous polyimide aerogels. However, when the input amount of ammonium chloride exceeds 10g, the structural integrity and mechanical strength of the porous polyimide aerogel are easily damaged, which is not conducive to the installation of the porous polyimide aerogel in the atomizer 2 , reduce the service life of liquid storage parts. Due to the excessive input of ammonium chloride, the agglomeration of the ammonium chloride granular pore-forming agent becomes more serious, which reduces the fluidity and uniformity of the PAA-NH 4 Cl slurry, thereby causing the structure of the porous polyimide aerogel to appear. Incomplete defects.

具体的,在步骤S05中,热亚胺化处理的升温速率为1~5℃/min,有利于羧基和亚胺充分脱水缩合反应,减少多孔聚酰亚胺气凝胶中疏液基团的数量。Specifically, in step S05, the temperature rise rate of the thermal imidization treatment is 1 to 5°C/min, which is conducive to the full dehydration and condensation reaction of carboxyl groups and imines, and reduces the formation of lyophobic groups in the porous polyimide aerogel. quantity.

具体的,在步骤S05中,热亚胺化处理的温度为240~270℃,热亚胺化处理的时间为0.5~2h,使得多孔聚酰亚胺气凝胶具有完整的外观形状、较强的力学强度、优异的储液性能和较快的吸液速率。热亚胺化处理的温度过高或过低,导致PAA热亚胺化不充分,从而造成多孔聚酰亚胺气凝胶的力学强度和吸液速率下降。Specifically, in step S05, the temperature of the thermal imidization treatment is 240-270°C, and the time of the thermal imidization treatment is 0.5-2h, so that the porous polyimide aerogel has a complete appearance shape and strong Excellent mechanical strength, excellent liquid storage performance and fast liquid absorption rate. The temperature of the thermal imidization treatment is too high or too low, resulting in insufficient thermal imidization of PAA, resulting in a decrease in the mechanical strength and liquid absorption rate of the porous polyimide aerogel.

具体的,在步骤S02中,添加的含氟芳香二酐单体和二胺单体为等摩尔比。在相同条件下,以等摩尔比的ODA/6FDA作为溶质,其含量越低,储液量越高,主要归结于在冷冻干燥和热亚胺化过程中,液相溶剂和固态氯化铵颗粒同时作为造孔剂并分别起到造孔的作用,提高了多孔聚酰亚胺气凝胶的孔隙率。但是当等摩尔比的ODA/6FDA含量小于10%时,柱状多孔聚酰亚胺气凝胶易出现结构坍塌、亲油慢以及易碎等不良现象。而等摩尔比的ODA/6FDA含量大于20%时,造孔剂相对降低,故亲油变慢以及储液量变低。由此可知,等摩尔比的ODA/6FDA在整个体系的溶质含量应当控制在10~20%较佳。因此,在步骤S02中,反应生成的所述聚酰胺酸溶液占含氟芳香二酐单体和二胺单体的质量百分比为10~20%。Specifically, in step S02, the added fluorine-containing aromatic dianhydride monomer and diamine monomer are in an equal molar ratio. Under the same conditions, using an equal molar ratio of ODA/6FDA as the solute, the lower its content, the higher the liquid storage volume, which is mainly due to the difference between the liquid solvent and the solid ammonium chloride particles during the freeze-drying and thermal imidization processes. At the same time, it serves as a pore-forming agent and plays the role of pore-forming respectively, improving the porosity of the porous polyimide aerogel. However, when the equimolar ratio of ODA/6FDA is less than 10%, columnar porous polyimide aerogels are prone to structural collapse, slow lipophilicity, and brittleness. When the equal molar ratio of ODA/6FDA is greater than 20%, the pore-forming agent is relatively reduced, so the lipophilicity becomes slower and the liquid storage volume becomes lower. It can be seen that the solute content of the equal molar ratio of ODA/6FDA in the entire system should be controlled at 10 to 20%. Therefore, in step S02, the polyamic acid solution generated by the reaction accounts for 10 to 20% of the mass percentage of the fluorinated aromatic dianhydride monomer and diamine monomer.

实施例1Example 1

向带有机械搅拌的三口烧瓶中加入一定量二氧六环(Diox)和叔丁醇,混合得到TBA溶液,调配TBA体积分数为0的混合溶剂溶液,然后添加等摩尔比的4,4'-二氨基二苯醚(ODA)和4,4'-(六氟异丙烯)二酞酸酐(6FDA),待固体完全溶解后形成10wt%的聚酰胺酸(PAA)溶液;Add a certain amount of dioxane (Diox) and tert-butyl alcohol to a three-necked flask with mechanical stirring, mix to obtain a TBA solution, prepare a mixed solvent solution with a TBA volume fraction of 0, and then add an equal molar ratio of 4,4' - Diaminodiphenyl ether (ODA) and 4,4'-(hexafluoroisopropylene) diphthalic anhydride (6FDA), after the solids are completely dissolved, a 10wt% polyamic acid (PAA) solution is formed;

(2)向制得的PAA溶液中添加10g粒径为140μm的氯化铵(NH4Cl)作为造孔剂,搅拌均匀后形成PAA-NH4Cl悬浊液,将PAA-NH4Cl悬浊液倒入模具中进行冷冻成柱状(冷冻速率为7℃/min),然后通过冷冻干燥法,以形成PAA-NH4Cl气凝胶;(2) Add 10g of ammonium chloride (NH 4 Cl) with a particle size of 140 μm as a pore-forming agent to the prepared PAA solution, stir evenly to form a PAA-NH4Cl suspension, and add the PAA-NH 4 Cl suspension Pour into a mold and freeze into a columnar shape (freezing rate is 7°C/min), and then freeze-dry to form PAA-NH 4 Cl aerogel;

(3)将PAA-NH4Cl气凝胶在5℃/min的升温速率,加热到240℃进行热亚胺化处理0.5h,得到多孔聚酰亚胺气凝胶样品。(3) Heat the PAA-NH 4 Cl aerogel to 240°C at a heating rate of 5°C/min for thermal imidization treatment for 0.5h to obtain a porous polyimide aerogel sample.

实施例2、实施例3、实施例4、实施例5与实施例1的区别在于调配的TBA体积分数不同,其它的均相同。其中,实施例2中调配出TBA体积分数为10%的混合溶剂溶液,实施例3中调配出TBA体积分数为20%的混合溶剂溶液,实施例4中调配出TBA体积分数为30%的混合溶剂溶液,实施例5中调配出TBA体积分数为40%的混合溶剂溶液,并以多孔陶瓷样品作为对比例1。分别观察实施例1至5和对比例1中的样品形状,并分别测试实施例1至5和对比例1中的样品结构强度和比表面积。The difference between Example 2, Example 3, Example 4, Example 5 and Example 1 lies in the volume fraction of the prepared TBA, and everything else is the same. Among them, in Example 2, a mixed solvent solution with a TBA volume fraction of 10% was prepared, in Example 3, a mixed solvent solution with a TBA volume fraction of 20% was prepared, and in Example 4, a mixed solvent solution with a TBA volume fraction of 30% was prepared. Solvent solution: In Example 5, a mixed solvent solution with a TBA volume fraction of 40% was prepared, and a porous ceramic sample was used as Comparative Example 1. The shapes of the samples in Examples 1 to 5 and Comparative Example 1 were respectively observed, and the structural strength and specific surface area of the samples in Examples 1 to 5 and Comparative Example 1 were tested respectively.

表1实施例1至5和对比例1的样品相关性能测试表Table 1 Sample related performance test table of Examples 1 to 5 and Comparative Example 1

实施例6Example 6

(1)向带有机械搅拌的三口烧瓶中加入47.79mL二氧六环(Diox)和20.48mL叔丁醇(TBA)溶液,TBA的体积占比为30%,之后添加等摩尔比的4,4'-二氨基二苯醚(ODA)和4,4'-(六氟异丙烯)二酞酸酐(6FDA),待固体完全溶解后形成10wt%的聚酰胺酸(PAA)溶液;(1) Add 47.79mL dioxane (Diox) and 20.48mL tert-butyl alcohol (TBA) solution to a three-necked flask with mechanical stirring. The volume ratio of TBA is 30%, and then add an equal molar ratio of 4, 4'-diaminodiphenyl ether (ODA) and 4,4'-(hexafluoroisopropylene) diphthalic anhydride (6FDA), after the solids are completely dissolved, a 10wt% polyamic acid (PAA) solution is formed;

(2)向制得的PAA溶液中添加粒径为170μm的10g氯化铵(NH4Cl)作为造孔剂,搅拌均匀后形成PAA-NH4Cl悬浊液;(2) Add 10g ammonium chloride (NH 4 Cl) with a particle size of 170 μm as a pore-forming agent to the prepared PAA solution, and stir evenly to form a PAA-NH4Cl suspension;

(3)将制得的PAA-NH4Cl悬浊液倒入模具中进行冷冻(冷冻速率为7℃/min),然后冷冻干燥24h以形成PAA-NH4Cl气凝胶;(3) Pour the prepared PAA-NH 4 Cl suspension into a mold, freeze it (freezing rate is 7°C/min), and then freeze-dry for 24 hours to form PAA-NH 4 Cl aerogel;

(4)PAA-NH4Cl气凝胶在5℃/min的升温速率,加热到240℃进行热亚胺化处理0.5h,得到多孔聚酰亚胺(PI)气凝胶样品。(4) The PAA-NH 4 Cl aerogel was heated to 240°C at a heating rate of 5°C/min for thermal imidization treatment for 0.5h to obtain a porous polyimide (PI) aerogel sample.

实施例7、实施例8、实施例9、实施例10与实施例6的区别在于向PAA溶液中添加氯化铵(NH4Cl)的粒径不同,其它的均相同。其中,实施例7中向PAA溶液中添加氯化铵(NH4Cl)的粒径为140μm,实施例8中向PAA溶液中添加氯化铵(NH4Cl)的粒径为110μm,实施例9中向PAA溶液中添加氯化铵(NH4Cl)的粒径为80μm,实施例10中向PAA溶液中添加氯化铵(NH4Cl)的粒径为60μm。分别观察实施例7至10中的样品形状和浆料是否分层,并分别测试实施例7至10中的样品孔径和抗压强度。The difference between Example 7, Example 8, Example 9, Example 10 and Example 6 lies in the particle size of ammonium chloride (NH 4 Cl) added to the PAA solution, and everything else is the same. Among them, the particle size of ammonium chloride (NH 4 Cl) added to the PAA solution in Example 7 is 140 μm, and the particle size of ammonium chloride (NH 4 Cl) added to the PAA solution in Example 8 is 110 μm. In Example 9, the particle size of the ammonium chloride (NH 4 Cl) added to the PAA solution was 80 μm. In Example 10, the particle size of the ammonium chloride (NH 4 Cl) added to the PAA solution was 60 μm. Observe the shape of the samples in Examples 7 to 10 and whether the slurry is delaminated, and test the pore size and compressive strength of the samples in Examples 7 to 10 respectively.

表2实施例7至10中的样品相关性能测试表Table 2 Sample related performance test table in Examples 7 to 10

测试项目Test items NH4Cl的D90粒径(um)D90 particle size of NH 4 Cl (um) 柱状PI完整性Column PI integrity 浆料是否分层Is the slurry layered? 孔径(um)Aperture (um) 力学强度Mechanical strength 实施例6Example 6 170170 不完整incomplete yes 100-120100-120 weak 实施例7Example 7 140140 完整whole no 80-10080-100 powerful 实施例8Example 8 110110 完整whole no 60-8060-80 powerful 实施例9Example 9 8080 完整whole no 40-6040-60 powerful 实施例10Example 10 6060 完整whole no 20-4020-40 powerful

以上所述仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明的保护范围之内。The above descriptions are only preferred embodiments of the present invention and are not intended to limit the present invention. Any modifications, equivalent substitutions and improvements made within the spirit and principles of the present invention shall be included in the protection of the present invention. within the range.

Claims (16)

1. The liquid storage piece is used for an atomizer and is characterized by comprising an atomization bullet main body and an atomization core used for atomizing atomized liquid to form aerosol, wherein the atomization core is arranged in the atomization bullet main body, a liquid storage cavity is formed in the atomization bullet main body, and the liquid storage piece is arranged in the liquid storage cavity; the liquid storage piece is porous aerogel, so that the liquid storage piece can be used for storing atomized liquid, and the liquid storage piece can transmit the stored atomized liquid to the atomization core.
2. The reservoir of claim 1, wherein the porous aerogel is a porous aerogel matrix made of polyimide.
3. The reservoir of claim 1, wherein the porous aerogel has a stock solution amount of 800-1000 mg/g.
4. A reservoir according to claim 1, wherein the porous aerogel has a pore size of 0.1 to 100 μm.
5. A reservoir according to any one of claims 1 to 4, wherein the porous aerogel is cylindrical, and wherein the porous aerogel is provided with a sleeve aperture extending axially therethrough, and wherein the atomizing core is located in the sleeve aperture.
6. The fluid storage element of claim 5, wherein the outer peripheral surface of the porous aerogel abuts against the inner side surface of the fluid storage chamber, and the walls of the sleeve holes abut against the outer peripheral surface of the atomizing core.
7. A nebulizer comprising a reservoir according to any one of claims 1 to 6.
8. The atomizer of claim 7 wherein said atomizing core comprises an atomizing support disposed in said atomizing bomb body, a heat generating body disposed in said atomizing support, and a liquid guiding member for conveying atomized liquid to said heat generating body, said liquid guiding member being disposed in said atomizing support, said atomizing support being provided with a liquid guiding port for conveying atomized liquid to said liquid guiding member, said porous aerogel shielding said liquid guiding port.
9. The atomizer of claim 7 wherein said atomizer body comprises an atomizer housing having an air inlet, a base disposed on an opening in a bottom of said atomizer housing, and a vent tube disposed in said atomizer housing, said atomizer core being supported on said base, said vent tube connecting said atomizer core with said air inlet, said atomizer housing defining said reservoir within said atomizer core and outside said vent tube, said atomizer core having a liquid port communicating with said reservoir, said porous aerogel closing said liquid port.
10. An aerosol generating device comprising a reservoir as claimed in any one of claims 1 to 5 or a nebuliser as claimed in any one of claims 6 to 9.
11. The preparation method of the liquid storage piece is characterized by comprising the following steps of:
step S01: mixing dioxane and tertiary butanol solution to obtain a mixed solvent;
step S02: adding fluorine-containing aromatic dianhydride monomer and diamine monomer into the mixed solvent, and obtaining polyamic acid solution through ammonolysis reaction of ether;
step S03: ammonium chloride particles are added into the polyamic acid solution and stirred uniformly to obtain PAA-NH 4 Cl suspension
Step S04: the PAA-NH is processed 4 Injecting the Cl suspension into a mold for freezing, and performing freeze drying treatment to obtain PAA-NH 4 Cl aerogel;
step S05: the PAA-NH after demoulding 4 Heating the Cl aerogel, and performing thermal imidization treatment to obtain the porous polyimide aerogel serving as a liquid storage part.
12. The method of preparing a reservoir according to claim 11, wherein in the step S01, the tertiary butanol solution occupies 0 to 30% of the volume specific gravity of the mixed solvent.
13. The method of preparing a reservoir according to claim 11, wherein in the step S03, the ammonium chloride particles have a particle size of 60 to 140 μm.
14. The method of producing a reservoir according to claim 11, wherein in the step S03, the ammonium chloride particles are added in an amount of 1 to 10g by mass.
15. The method of preparing a liquid storage member according to claim 11, wherein in said step S05, the thermal imidization treatment is performed at a temperature of 240 to 270 ℃ for a time of 0.5 to 2 hours.
16. The method of claim 11, wherein in the step S02, the polyamic acid solution formed by the reaction accounts for 10 to 20% by mass of the fluorine-containing aromatic dianhydride monomer and the diamine monomer.
CN202310798063.5A 2023-06-30 2023-06-30 Liquid storage part, atomizer, aerosol generating device and liquid storage part preparation method Pending CN116784529A (en)

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