CN105624759A - Ceramic membrane with capillary structure and super dehumidifying and wetting performance and preparation method thereof - Google Patents

Ceramic membrane with capillary structure and super dehumidifying and wetting performance and preparation method thereof Download PDF

Info

Publication number
CN105624759A
CN105624759A CN201511010377.6A CN201511010377A CN105624759A CN 105624759 A CN105624759 A CN 105624759A CN 201511010377 A CN201511010377 A CN 201511010377A CN 105624759 A CN105624759 A CN 105624759A
Authority
CN
China
Prior art keywords
ceramic membrane
water
ceramic
mass percent
super
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.)
Granted
Application number
CN201511010377.6A
Other languages
Chinese (zh)
Other versions
CN105624759B (en
Inventor
谢贤宁
林群
张顺中
刘颖丹
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ULTRAPOWER ELECTRICS Co Ltd
Original Assignee
ULTRAPOWER ELECTRICS Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by ULTRAPOWER ELECTRICS Co Ltd filed Critical ULTRAPOWER ELECTRICS Co Ltd
Priority to CN201511010377.6A priority Critical patent/CN105624759B/en
Publication of CN105624759A publication Critical patent/CN105624759A/en
Application granted granted Critical
Publication of CN105624759B publication Critical patent/CN105624759B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/12Anodising more than once, e.g. in different baths
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/10Sintering only
    • B22F3/11Making porous workpieces or articles
    • B22F3/1103Making porous workpieces or articles with particular physical characteristics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/10Sintering only
    • B22F3/11Making porous workpieces or articles
    • B22F3/1121Making porous workpieces or articles by using decomposable, meltable or sublimatable fillers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F7/00Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
    • B22F7/002Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of porous nature
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/06Anodisation of aluminium or alloys based thereon characterised by the electrolytes used
    • C25D11/10Anodisation of aluminium or alloys based thereon characterised by the electrolytes used containing organic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Composite Materials (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The invention provides a ceramic membrane with a capillary structure and super dehumidifying and wetting performance. The thickness of the ceramic membrane ranges from 10 nm to 600 micrometers. The ceramic membrane comprises an aluminum compound substrate and a base membrane layer adhering to the substrate. The base membrane layer is an aluminum oxide ceramic layer. The ceramic membrane is a porous membrane with the average capillary radius of 0.1 mm to 1.2 mm, water drops with unit mass can be completely spread through the hydrophilic surface of the ceramic membrane, and a water membrane with the area not smaller than 300 cm<2>/g is formed. By means of the hydrophilic surface, water molecules can overcome self gravity, and the climbing height in the vertical direction is not smaller than 3.0 cm.

Description

具有毛细结构和超级抽湿浸润性能的陶瓷膜及其制备方法Ceramic membrane with capillary structure and super dehumidifying wettability and preparation method thereof

技术领域technical field

本发明涉及一种陶瓷膜的制备方法及其应用,尤其涉及一种具有毛细结构及超级浸润抽吸性能的陶瓷膜的制备及其应用。The invention relates to a preparation method and application of a ceramic membrane, in particular to a preparation and application of a ceramic membrane with a capillary structure and super-wetting suction performance.

背景技术Background technique

表面浸润性是固体表面的一个重要特征,通常以接触角来表征液体对固体的浸润程度。一般来说,固体表面与水的接触角大于90°时,称之为疏水表面;小于90°时,称之为亲水表面。近年来,也有人提出以65°接触角作为亲水和疏水的界限。Surface wettability is an important characteristic of solid surfaces, and the contact angle is usually used to characterize the wettability of liquids on solids. Generally speaking, when the contact angle between a solid surface and water is greater than 90°, it is called a hydrophobic surface; when it is less than 90°, it is called a hydrophilic surface. In recent years, it has also been proposed to use 65° contact angle as the boundary between hydrophilic and hydrophobic.

由于对液体良好的浸润性,亲水表面可广泛应用于工业与生活中。比如水蒸气凝结在亲水表面上时,容易展开为均匀连续的水膜,抑制孤立水滴的形成,能增强表面的抗雾性和透明性,这在需要防止结霜和保持透明(如冰箱内壁、汽车的挡风玻璃等)的应用中很重要。另外,空调的冷凝器散冷翅片在工作时,空气中的水蒸气会遇冷凝结在翅片间,形成水珠。这不仅降低了翅片和空气的热交换面积,而且也增大了风阻,严重影响空调的制冷效率。而在散冷翅片上涂布亲水材料,可防止凝结时水珠的形成,减小风阻,维持较大的换热面积,从而提高空调的能效。Due to its good wettability to liquids, hydrophilic surfaces can be widely used in industry and life. For example, when water vapor condenses on a hydrophilic surface, it is easy to expand into a uniform and continuous water film, inhibiting the formation of isolated water droplets, and enhancing the anti-fog and transparency of the surface, which is necessary to prevent frosting and maintain transparency (such as the inner wall of a refrigerator) , car windshield, etc.) is very important in the application. In addition, when the cooling fins of the condenser of the air conditioner are working, the water vapor in the air will condense between the fins and form water droplets. This not only reduces the heat exchange area between the fins and the air, but also increases the wind resistance, seriously affecting the cooling efficiency of the air conditioner. The coating of hydrophilic material on the cooling fins can prevent the formation of water droplets during condensation, reduce wind resistance, maintain a large heat exchange area, and thus improve the energy efficiency of the air conditioner.

溶胶-凝胶法是制备无机亲水涂层主要方法之一,反应可在较低的温度下进行,过程易调控,但该方法一般需要紫外光照射等方式才能获得亲水性。电化学方法(如电化学沉积、阳极氧化等)也可用于制备无机亲水涂层,但需要特殊的仪器设备,难以实现大面积表面的制备。有机亲水涂层多采用涂布的方法来获得,容易实现大规模生产,但涂层的亲水性能不够稳定,使用一定时间后会消失。The sol-gel method is one of the main methods for preparing inorganic hydrophilic coatings. The reaction can be carried out at a lower temperature, and the process is easy to control. However, this method generally requires ultraviolet light irradiation to obtain hydrophilicity. Electrochemical methods (such as electrochemical deposition, anodic oxidation, etc.) can also be used to prepare inorganic hydrophilic coatings, but special instruments and equipment are required, and it is difficult to achieve the preparation of large-area surfaces. Organic hydrophilic coatings are mostly obtained by coating, which is easy to realize large-scale production, but the hydrophilic property of the coating is not stable enough and will disappear after a certain period of use.

上述亲水表面的亲水性能都是用接触角来表征的,最常报道的接触角大多为0–30°之间。在目前论文及专利中,尚未见到一种亲水表面具有毛细结构,能够对水(或其它液体)产生超级浸润和抽吸作用。The hydrophilic properties of the above-mentioned hydrophilic surfaces are characterized by contact angles, and the most commonly reported contact angles are mostly between 0–30 ° . In the current papers and patents, a hydrophilic surface with a capillary structure has not been seen, which can produce super wetting and suction for water (or other liquids).

发明内容Contents of the invention

本发明的目的在于解决上述问题,提出一种具有毛细结构的陶瓷膜及其制备方法与应用。The purpose of the present invention is to solve the above problems, and propose a ceramic membrane with a capillary structure and its preparation method and application.

本发明的目的通过以下技术方案来实现:The purpose of the present invention is achieved through the following technical solutions:

具有毛细结构和超级抽湿浸润性能的陶瓷膜,所述陶瓷膜厚度为10nm~600μm,所述陶瓷膜包括一铝化合物基底、附着于所述基底上的基膜层,所述基膜层为氧化铝陶瓷层,所述陶瓷膜为具有平均毛细管半径为0.1-1.2mm的多孔膜,所述陶瓷膜亲水表面能使单位质量的水滴完全铺开,形成面积不小于300cm2/g的水膜;且亲水表面能使水分子克服自身重力,在垂直方向自行爬升的高度不小于3.0cm。A ceramic membrane with a capillary structure and super moisture absorption and wetting performance, the thickness of the ceramic membrane is 10 nm to 600 μm, the ceramic membrane includes an aluminum compound substrate, and a base film layer attached to the base, the base film layer is An alumina ceramic layer, the ceramic membrane is a porous membrane with an average capillary radius of 0.1-1.2 mm, and the hydrophilic surface of the ceramic membrane can completely spread water droplets per unit mass to form water with an area of not less than 300 cm 2 /g membrane; and the hydrophilic surface can make water molecules overcome their own gravity, and the height of self-climbing in the vertical direction is not less than 3.0cm.

优选地,所述的具有毛细结构的陶瓷膜的制备方法,包括如下步骤,Preferably, the preparation method of the ceramic membrane with a capillary structure comprises the following steps,

S1、基底预处理S1. Substrate pretreatment

S11、基底脱脂:将基材放入5%~20%的硫酸槽中,脱脂,3min~5min后取出;所述基材为铝基材或铝合金基材;S11. Base degreasing: put the base material in a 5%-20% sulfuric acid tank, degrease, and take it out after 3min-5min; the base material is an aluminum base material or an aluminum alloy base material;

S12、第一次水洗:用自来水反复冲洗铝基材,保证铝基材表面的PH值>5;S12, the first water washing: wash the aluminum substrate repeatedly with tap water to ensure that the pH value of the surface of the aluminum substrate is > 5;

S13、碱洗:将第一次水洗后的基材放入浓度为45kg/m3~55kg/m3,温度为40℃~60℃的氢氧化钠溶液中,碱洗4min~8min;S13. Alkali washing: put the substrate after the first water washing into a sodium hydroxide solution with a concentration of 45kg/m 3 to 55kg/m 3 and a temperature of 40°C to 60°C, and wash with alkali for 4min to 8min;

S14、第二次水洗:用自来水反复冲洗铝基材,冲洗2min~4min后取出;S14, the second water washing: wash the aluminum substrate repeatedly with tap water, take it out after rinsing for 2 minutes to 4 minutes;

S15、第三次水洗:用自来水反复冲洗铝基材,冲洗2min~4min,待PH值>5后取出;S15. The third water washing: wash the aluminum substrate repeatedly with tap water for 2-4 minutes, and take it out after the pH value is > 5;

S16、阳极氧化:用碱性电解液、和酸性电解液以先后顺序清洗氧化,促进金属铝基材表面生成具有孔隙高,吸附能力强的氧化铝膜,所述氧化铝膜厚度为0.3~30μm;S16. Anodizing: Clean and oxidize in sequence with alkaline electrolyte and acidic electrolyte to promote the formation of an aluminum oxide film with high porosity and strong adsorption capacity on the surface of the metal aluminum substrate. The thickness of the aluminum oxide film is 0.3-30 μm ;

S17、第四次水洗:将经过阳极氧化的氧化铝膜用自来水反复冲洗,冲洗2min~4min后取出,再用去离子水冲洗1min~2min;S17, the fourth water washing: wash the anodized aluminum oxide film repeatedly with tap water, take it out after rinsing for 2 minutes to 4 minutes, and then wash it with deionized water for 1 minute to 2 minutes;

S18、干燥:取出经化学氧化后的铝基材,经去离子水反复冲洗后干燥;S18. Drying: take out the chemically oxidized aluminum substrate, rinse it repeatedly with deionized water, and then dry it;

S2、氧化铝陶瓷层涂覆步骤;S2, alumina ceramic layer coating step;

S21、原料粉末准备;将α-氧化铝、有机成孔剂、烧结助剂和其他批料组分按比例进行称量配比:所述α-氧化铝质量百分比为60%-70%,粒径为5-30μm,所述有机成孔剂质量百分比为30%-40%,粒径为3-35μm;所述烧结助剂质量百分比为10%-30%;S21. Preparation of raw material powder; weighing and proportioning α-alumina, organic pore forming agent, sintering aid and other batch components: the mass percentage of α-alumina is 60%-70%, the grain The diameter is 5-30 μm, the mass percentage of the organic pore-forming agent is 30%-40%, and the particle size is 3-35 μm; the mass percentage of the sintering aid is 10%-30%;

S22、原料混合:先将α-氧化铝、有机成孔剂混合均匀后,再与烧结助剂和其他批料组分混合:α-氧化铝和有机成孔剂为70-90%、所述烧结助剂和其他批料组分为10-30%混合;S22. Mixing of raw materials: first mix α-alumina and organic pore-forming agent evenly, and then mix with sintering aid and other batch components: α-alumina and organic pore-forming agent are 70-90%, the The sintering aid and other batch components are mixed at 10-30%;

S23、混磨搅拌:在混合粉末中加入20-30粒直径为5-12mm的氧化铝陶瓷球或钢球,在混料机上混磨1-3h;S23, mixed grinding and stirring: add 20-30 alumina ceramic balls or steel balls with a diameter of 5-12 mm to the mixed powder, and mix and grind on the mixer for 1-3 hours;

S24、成型:将混合原料装入模具内进行低温预热成型,所述预热成型温度为180-250℃;S24. Molding: put the mixed raw materials into the mold for low-temperature preheating molding, and the preheating molding temperature is 180-250°C;

S25、中温烧结及成孔;将成型后的产品转入中温烧结炉内,加热至600℃,所述中温炉的加热时间为2-3h,保温1-2h,然后随炉冷却至100℃以下,最后从炉子中取出最后制得的多孔陶瓷。S25. Medium-temperature sintering and pore forming; transfer the formed product into a medium-temperature sintering furnace and heat it to 600°C. The heating time of the medium-temperature furnace is 2-3h, keep it warm for 1-2h, and then cool with the furnace to below 100°C , and finally remove the final porous ceramic from the furnace.

优选地,所述的具有毛细结构和超级抽湿浸润性能的陶瓷膜的制备方法,所述S16的阳极氧化步骤中,所述电解液包括酸性电解液与碱性电解液,所述酸性电解液配比为:甲酸质量百分比20~40%;草酸质量百分比30~50%;丙二酸质量百分比30~50%;硫酸镍质量百分比0~10%,处理参数为:氧化电压为20~80V,电流密度为2.0~3.5A/dm2,处理时间为0.5~3h,处理温度为10~25℃;Preferably, in the method for preparing a ceramic membrane having a capillary structure and super-wettability, in the anodizing step of S16, the electrolyte includes an acidic electrolyte and an alkaline electrolyte, and the acidic electrolyte The ratio is: 20-40% by mass of formic acid; 30-50% by mass of oxalic acid; 30-50% by mass of malonic acid; 0-10% by mass of nickel sulfate. The processing parameters are: the oxidation voltage is 20-80V, The current density is 2.0~3.5A/dm2, the treatment time is 0.5~3h, and the treatment temperature is 10~25℃;

所述碱性电解液配比为:碳酸钠质量百分比40~60%;铬酸钠质量百分比15~25%;氢氧化钠质量百分比2~5%;磷酸三钠质量百分比0~1.5%,处理参数为:氧化电压为5~35V,电流密度为1.0~2.5A/dm2,处理时间为5~60min,处理温度为85~100℃。The proportion of the alkaline electrolyte is: 40-60% by mass of sodium carbonate; 15-25% by mass of sodium chromate; 2-5% by mass of sodium hydroxide; 0-1.5% by mass of trisodium phosphate. The parameters are: the oxidation voltage is 5-35V, the current density is 1.0-2.5A/dm2, the treatment time is 5-60min, and the treatment temperature is 85-100°C.

优选地,所述S24低温成型中采用空气循环炉或平板炉,所述空气循环炉预热成型温度为180-250℃,低温成型时间为8-12min;所述平板炉预热成型温度为180-250℃,低温成型时间为3-5min。Preferably, the S24 low-temperature molding adopts an air circulation furnace or a flat furnace, the preheating temperature of the air circulation furnace is 180-250°C, and the low temperature molding time is 8-12min; the preheating temperature of the flat furnace is 180 -250℃, low temperature molding time is 3-5min.

优选地,所述S12中的第一次水洗冲洗时间为2min~4min。Preferably, the first water washing in S12 takes 2 minutes to 4 minutes.

优选地,所述S21中其他批料为分散溶剂。Preferably, the other batch materials in S21 are dispersion solvents.

优选地,所述混料机为V型结构的混料机,所述混料速度为100-150r/min。Preferably, the mixer is a V-shaped mixer, and the mixing speed is 100-150r/min.

本发明制备的陶瓷膜具有超级浸润,所述超级浸润是指亲水表面能使单位质量的水滴完全铺开,形成面积不小于300cm2/g的水膜;且所述陶瓷膜具有抽吸作用,所述抽吸作用是指亲水表面能使水分子克服自身重力,在垂直方向自行爬升的高度不小于3.0cm。The ceramic membrane prepared by the present invention has super wetting, and the super wetting means that the hydrophilic surface can completely spread the water droplets per unit mass to form a water film with an area of not less than 300 cm 2 /g; and the ceramic membrane has a suction effect , the suction effect means that the hydrophilic surface can make water molecules overcome their own gravity, and the height of self-climbing in the vertical direction is not less than 3.0cm.

本发明所述的陶瓷膜导热系数用德国耐驰TCT426测得。取长宽各30cm的陶瓷膜并将热线与热电偶插入两片试样间,接通2.0A加热电流开始测试。得到升温对时间的函数,由此得出陶瓷膜的导热系数为1.0–30W/m.K,与铝(或铝合金基底)的整体导热系数率可高达200W/m.K。陶瓷膜工作温度高达600℃,在干燥条件下的击穿电压高达DC5000V。该陶瓷膜具有毛细结构,其平均毛细管半径为0.1–1.2mm,对液体能产生很强的毛细管作用力,尤其是对水能产生超级浸润抽吸作用。The thermal conductivity of the ceramic film described in the present invention is measured by German Netzsch TCT426. Take a ceramic film of 30cm in length and width, insert a hot wire and a thermocouple between two samples, and turn on a heating current of 2.0A to start the test. The function of temperature rise to time is obtained, and the thermal conductivity of the ceramic film is 1.0-30W/m.K, and the overall thermal conductivity of the aluminum (or aluminum alloy substrate) can be as high as 200W/m.K. The working temperature of the ceramic membrane is as high as 600°C, and the breakdown voltage is as high as DC5000V under dry conditions. The ceramic membrane has a capillary structure, and its average capillary radius is 0.1-1.2mm, which can generate a strong capillary force for liquids, especially super-wetting suction for water.

本发明所述的超级浸润作用,是指在常温常压下,当一滴水(体积约为0.03cm3;质量约为0.03g)滴落到本发明涉及的陶瓷膜上时(陶瓷膜为水平放置),水滴不能稳定存在,而是自发地向四周扩散铺展开,完全浸润陶瓷膜表面,于数分钟内在陶瓷膜上形成连续均匀的水膜,水膜与陶瓷膜表面的接触面积可高达40cm2,也就是说,水膜与大气的接触面积可高达40cm2。概括而言,单位质量的水滴在陶瓷膜上铺开形成水膜后,水膜的厚度最薄可达7.5μm/g,其与大气的接触面积在300–1333cm2/g之间。陶瓷膜对其它液体也有类似超级浸润作用。The superwetting effect described in the present invention refers to that at normal temperature and pressure, when a drop of water (volume is about 0.03cm3 ; quality is about 0.03g) drops on the ceramic membrane involved in the present invention (the ceramic membrane is horizontal placed), the water droplets cannot exist stably, but spread spontaneously to the surroundings, completely infiltrate the surface of the ceramic membrane, and form a continuous and uniform water film on the ceramic membrane within a few minutes. The contact area between the water film and the surface of the ceramic membrane can be as high as 40cm 2 , that is to say, the contact area between the water film and the atmosphere can be as high as 40cm 2 . In a nutshell, after water droplets per unit mass are spread on the ceramic membrane to form a water film, the thickness of the water film can be as thin as 7.5 μm/g, and the contact area with the atmosphere is between 300–1333 cm 2 /g. Ceramic membranes also have a similar superwetting effect on other liquids.

本发明所述的陶瓷膜超级抽吸作用,是指在常温常压下,当把陶瓷膜垂直浸入水中时,由于陶瓷膜毛细管的抽吸作用,水能够克服自身的重力,沿着陶瓷膜向上爬升,爬升高度一般高于液面3.0-12.0cm。陶瓷膜对其它液体也有类似超级抽吸作用。The super suction effect of the ceramic membrane in the present invention means that at normal temperature and pressure, when the ceramic membrane is vertically immersed in water, due to the suction effect of the capillary of the ceramic membrane, the water can overcome its own gravity and move upward along the ceramic membrane. Climbing, the climbing height is generally 3.0-12.0cm higher than the liquid level. The ceramic membrane also has a similar super suction effect on other liquids.

本发明的有益效果主要体现在:本发明利用电化学氧化和浆料涂覆相结合的方法在铝(或铝合金)表面制备了具有毛细结构的陶瓷膜,该陶瓷膜导热性能好,热稳定性高,尤其是对水(等液体)具有超级浸润和抽吸作用。这些作用拓展了现有亲水材料的特性和功能,并为亲水材料开辟了新的应用领域,如制冷降温、海水淡化、以及电子元器件的导热散热等。The beneficial effects of the present invention are mainly reflected in: the present invention uses the method of combining electrochemical oxidation and slurry coating to prepare a ceramic film with a capillary structure on the surface of aluminum (or aluminum alloy), and the ceramic film has good thermal conductivity and thermal stability High performance, especially for water (and other liquids) with super wetting and suction. These effects expand the characteristics and functions of existing hydrophilic materials, and open up new application fields for hydrophilic materials, such as refrigeration and cooling, seawater desalination, and heat conduction and heat dissipation of electronic components.

附图说明Description of drawings

下面结合附图对本发明技术方案作进一步说明:Below in conjunction with accompanying drawing, technical solution of the present invention will be further described:

图1:基于陶瓷膜的制冷器结构图,此时隐藏掉了制冷器的翅片。Figure 1: Structural diagram of a ceramic membrane-based cooler with the fins of the cooler hidden.

具体实施方式detailed description

在本发明中,除了可以在箔、片、板等形状的铝(或铝合金)平面基底上制备陶瓷膜,也可在铝(或铝合金)丝线等非平面结构上制备得到陶瓷膜,陶瓷膜应用于各种场合。对于基底的形状并无特殊限制。In the present invention, in addition to preparing ceramic films on aluminum (or aluminum alloy) planar substrates in the shape of foils, sheets, plates, etc., ceramic films can also be prepared on non-planar structures such as aluminum (or aluminum alloy) wires. Membranes are used in various occasions. There is no particular limitation on the shape of the base.

由于陶瓷膜的超级浸润功能,水滴在陶瓷膜上形成水的膜与空气的接触面积高达300–1333cm2/g,即水膜与陶瓷膜和空气的热交换面积大,因此水膜很容易从环境吸热蒸发,由液体变为气体。同时由于水膜的厚度非常薄(最薄可达7.5μm/g),在厚度方向的温度梯度小,这有利于水膜的快速吸热和快速蒸发。再者,陶瓷膜有良好的导热性能,水吸热蒸发后,陶瓷膜及铝(或铝合金)基底的温度迅速降低,因此陶瓷膜可首先应用于制冷降温。陶瓷膜用于制冷降温的优点是节约能源,效率高以及简单方便。Due to the super-wetting function of the ceramic membrane, the contact area between the water film and the air formed by water droplets on the ceramic membrane is as high as 300–1333cm 2 /g, that is, the heat exchange area between the water film, the ceramic film and the air is large, so the water film is easy to get from The environment absorbs heat and evaporates, changing from liquid to gas. At the same time, because the thickness of the water film is very thin (the thinnest can reach 7.5 μm/g), the temperature gradient in the thickness direction is small, which is conducive to the rapid heat absorption and rapid evaporation of the water film. Furthermore, the ceramic membrane has good thermal conductivity. After the water absorbs heat and evaporates, the temperature of the ceramic membrane and the aluminum (or aluminum alloy) substrate drops rapidly. Therefore, the ceramic membrane can be firstly used for cooling. The advantages of ceramic membranes for refrigeration and cooling are energy saving, high efficiency, and simplicity and convenience.

陶瓷膜对水的超级浸润性能测试Super wettability test of ceramic membrane to water

制备宽度约为10.0cm的以铝箔为基底的陶瓷膜,当用滴管往陶瓷膜上滴一滴水时(质量约为0.03g,体积约为0.03cm3),水滴不能稳定存在,而是在1s内铺开形成直径约为2.0cm的水膜。此水膜继续扩散,过了32s后,直径增大到了5.2cm。当上述水膜继续扩散,在60s后,直径增大到了6.3cm。此时液膜与陶瓷膜的接触面积约为30.2cm2,所对应的单位质量接触面积为996.6cm2/g,单位质量水膜厚度为10.0μm/g。Prepare a ceramic film with a width of about 10.0 cm based on aluminum foil. When a drop of water (mass is about 0.03 g, volume is about 0.03 cm 3 ) is dropped on the ceramic film with a dropper, the water drop cannot exist stably. Spread within 1s to form a water film with a diameter of about 2.0cm. The water film continued to spread, and after 32 seconds, the diameter increased to 5.2cm. When the above water film continued to spread, after 60s, the diameter increased to 6.3cm. At this time, the contact area between the liquid film and the ceramic film is about 30.2 cm 2 , the corresponding contact area per unit mass is 996.6 cm 2 /g, and the thickness of the water film per unit mass is 10.0 μm/g.

陶瓷膜毛细管半径计算Calculation of Capillary Radius of Ceramic Membrane

将一片长为20cm、宽为5cm陶瓷膜垂直浸入水中2cm,长度方向保持与水面垂直,有18cm的陶瓷膜高于水面,由此观察水沿着陶瓷膜表面的倒吸现象。60min后,发现水在垂直方向的倒吸高度为h=12cm。根据公式计算陶瓷膜内毛细管的平均半径r,所述公式中α=72.8mN/m为水的表面张力系数;=20°为毛细管内液面的接触角;ρ=1000kg/m3为水的密度;g=9.8m/s2为重力加速度,得到r=0.1mm。A ceramic membrane with a length of 20cm and a width of 5cm is vertically immersed in water for 2cm, the length direction is kept perpendicular to the water surface, and 18cm of the ceramic membrane is higher than the water surface, so as to observe the phenomenon of water sucking back along the surface of the ceramic membrane. After 60 minutes, it was found that the water suck back height in the vertical direction was h=12cm. According to the formula Calculating the average radius r of the capillary in the ceramic membrane, in the formula, α=72.8mN/m is the surface tension coefficient of water; =20 ° is the contact angle of the liquid surface in the capillary; ρ=1000kg/m 3 is the density of water; g=9.8m/s 2 is the acceleration due to gravity, and r=0.1mm is obtained.

采用上述方法对本发明中所制备的不同厚度、不同成分的陶瓷膜进行测量计算,得到毛细管半径在0.1–1.2mm之间。The above method is used to measure and calculate the ceramic membranes prepared in the present invention with different thicknesses and different components, and the capillary radius is obtained to be between 0.1-1.2 mm.

陶瓷膜上水膜蒸发性能比较Comparison of Evaporation Performance of Water Film on Ceramic Membrane

由于水滴能在陶瓷膜上完全铺开形成很薄的水膜,水膜与空气的接触面积在300–1333cm2/g之间,因此相对于同等质量的水滴,水膜的蒸发速度大幅提高。在相同的环境风速1.0m/s和环境相对湿度65%的条件下,测量了水在不同温度下蒸发所需时间。Since the water droplets can spread completely on the ceramic membrane to form a very thin water film, the contact area between the water film and the air is between 300-1333cm 2 /g, so compared with the water droplets of the same mass, the evaporation rate of the water film is greatly increased. Under the same ambient wind speed of 1.0m/s and ambient relative humidity of 65%, the time required for water to evaporate at different temperatures was measured.

表1比较了1滴水(约0.03g)在10×10cm2陶瓷膜上(样品#1)和在10×10cm2铝箔上(样品#2)完全蒸发所需时间(所述温度指的是陶瓷膜表面和铝箔表面的温度)。Table 1 compares the time required for 1 drop of water (approximately 0.03g) to completely evaporate on a 10×10cm 2 ceramic film (sample #1) and on a 10×10cm 2 aluminum foil (sample #2) (the temperature refers to the ceramic temperature of film surface and aluminum foil surface).

由表1数据可见,在20–90℃的温度范围内,水膜的蒸发速度是水滴蒸发速度的10倍以上。尤其是在20℃,水膜只需4–5min即可完全蒸发,而水滴则至少需要60min以上才能蒸发完全。It can be seen from the data in Table 1 that in the temperature range of 20–90°C, the evaporation rate of the water film is more than 10 times that of the water droplet. Especially at 20°C, it only takes 4-5 minutes for the water film to evaporate completely, while it takes at least 60 minutes for the water droplets to evaporate completely.

表1:Table 1:

在相同的环境相对湿度65%的条件下,测量水在不同环境风速、不同表面温度下蒸发所需时间。Under the same ambient relative humidity of 65%, measure the time required for water to evaporate under different ambient wind speeds and different surface temperatures.

表2比较了1滴水(约0.03g)在10×10cm2陶瓷膜上(样品#1)和在10×10cm2铝箔上(样品#2)完全蒸发所需时间(所述温度指的是陶瓷膜表面和铝箔表面的温度)。Table 2 compares the time required for 1 drop of water (about 0.03g) to completely evaporate on a 10× 10cm2 ceramic film (sample #1) and on a 10× 10cm2 aluminum foil (sample#2) (the temperature refers to the ceramic temperature of film surface and aluminum foil surface).

表2:Table 2:

陶瓷膜的应用一:Application of ceramic membrane 1:

如图1所示,为基于陶瓷膜的制冷器结构图,所述制冷原理为在金属(铝、铜、不锈钢等)真空蒸发腔1的内壁有陶瓷膜,适量的水由电磁阀2控制通过进水管3进入蒸发腔1后,迅速在陶瓷膜上形成水膜,水膜与真空的接触面很大,在真空状态下很快蒸发变为气体,从出气管4被水气两用泵5抽出蒸发腔到达集水箱6。然后水滴又由进水管3输入,在蒸发腔内重复水膜形成、蒸发、排出的过程,如此循环往复,循环的周期由电磁阀的开启与关闭来控制。水膜蒸发时从环境大量吸热,例如1.0g水蒸发要吸收大于2000J的热量,所吸收热量能使100g的铝片降温10℃。因此水膜的快速蒸发使得蒸发腔表面的温度明显下降,该降温作用又由翅片传递到环境空气中,从而到达降低环境温度的制冷效果。As shown in Figure 1, it is a structural diagram of a refrigerator based on a ceramic membrane. The refrigeration principle is that there is a ceramic membrane on the inner wall of a metal (aluminum, copper, stainless steel, etc.) vacuum evaporation chamber 1, and an appropriate amount of water is controlled by a solenoid valve 2. After the water inlet pipe 3 enters the evaporation chamber 1, a water film is quickly formed on the ceramic membrane. The contact surface between the water film and the vacuum is very large, and it evaporates quickly in a vacuum state and becomes gas. Draw out the evaporation chamber to reach the water collection tank 6. Then the water droplets are input from the water inlet pipe 3, and the process of forming, evaporating, and discharging the water film is repeated in the evaporation chamber, and this cycle goes on and on, and the cycle period is controlled by the opening and closing of the solenoid valve. When the water film evaporates, it absorbs a large amount of heat from the environment. For example, 1.0g of water evaporates to absorb more than 2000J of heat, and the absorbed heat can reduce the temperature of 100g of aluminum sheet by 10°C. Therefore, the rapid evaporation of the water film causes the temperature on the surface of the evaporation chamber to drop significantly, and the cooling effect is transmitted to the ambient air by the fins, thereby achieving the cooling effect of reducing the ambient temperature.

具体而言,制得一个铝制蒸发腔,腔体内部体积为12cm×6cm×2cm,当水膜在最高负压为80KPa的真空度下蒸发时,产生了明显的吸热降温效果:在2–3min内,腔体外表面温度由原先的25℃迅速降低到了14℃,降温幅度大于10℃。Specifically, an aluminum evaporation chamber was fabricated with an internal volume of 12cm×6cm×2cm. When the water film was evaporated under a vacuum with a maximum negative pressure of 80KPa, it produced an obvious heat-absorbing and cooling effect: at 2 Within -3 minutes, the temperature of the outer surface of the cavity dropped rapidly from the original 25°C to 14°C, and the temperature drop was greater than 10°C.

在上述制冷过程中,陶瓷膜起到了关键作用:第一,在陶瓷膜上形成的水膜,其厚度可薄到10μm,这减小了水膜在厚度方向的温度梯度,使其能够快速吸热蒸发。如果水膜厚度过大,由于水的导热系数很小(20℃时约为0.6W/m.K),在厚度方向的温度梯度会很大、热传递会很慢,从而影响水的吸热蒸发速度。第二,陶瓷膜及铝(或铝合金)基底的平均导热系数率高达200W/m.K,良好的导热性保证了水膜能从蒸发腔体表面快速吸热,使腔体外表面以及相连翅片的温度明显下降,达到制冷的目的。In the above refrigeration process, the ceramic membrane plays a key role: first, the thickness of the water film formed on the ceramic membrane can be as thin as 10 μm, which reduces the temperature gradient of the water film in the thickness direction and enables it to absorb quickly. Thermal evaporation. If the thickness of the water film is too large, due to the small thermal conductivity of water (about 0.6W/m.K at 20°C), the temperature gradient in the thickness direction will be large and the heat transfer will be slow, which will affect the heat absorption and evaporation rate of water. . Second, the average thermal conductivity of the ceramic film and aluminum (or aluminum alloy) substrate is as high as 200W/m.K. Good thermal conductivity ensures that the water film can quickly absorb heat from the surface of the evaporation chamber, making the outer surface of the chamber and the connected fins The temperature drops significantly, achieving the purpose of refrigeration.

陶瓷膜的应用二Application of Ceramic Membrane II

基于陶瓷膜的海水淡化原理与装置和制冷器原理与结构很相似,同样是在一个真空腔体的内壁上制备有陶瓷膜,由导水管将适量海水引入真空腔体,海水进入腔体后在陶瓷膜上浸润铺开,与真空的接触面积最大化。同时由于腔体内的真空度,海水中的水分迅速蒸发为水蒸气,经由水气两用真空泵抽送到预先装有淡水的集水箱中。由于在陶瓷膜上形成的水膜的厚度很薄,水膜在真空状态下于常温(20–30℃)便可迅速蒸发,无需额外加热升温,且水膜蒸发对真空度的要求也不高,负压为80KPa的真空度即可维持快速的蒸发与淡水收集。因此,应用陶瓷膜的海水淡化技术的优点为:节能环保,结构装置简单,便于维护,成本低,用过的陶瓷膜可洗净后循环利用,所得到的淡水纯度高。在此海水淡化技术中,海水的蒸发在常温就可进行,既不需要价格昂贵的反渗透膜,也不需要耗费太多电能把海水加热到沸点进行蒸发。The principle and structure of seawater desalination based on ceramic membrane are very similar to the principle and structure of the device and refrigerator. A ceramic membrane is also prepared on the inner wall of a vacuum chamber, and an appropriate amount of seawater is introduced into the vacuum chamber by the aqueduct. Wetting spreads on the ceramic membrane to maximize the contact area with the vacuum. At the same time, due to the vacuum in the cavity, the water in the seawater evaporates quickly into water vapor, which is pumped into the water collection tank pre-installed with fresh water through the water-air dual-purpose vacuum pump. Since the thickness of the water film formed on the ceramic membrane is very thin, the water film can evaporate rapidly at room temperature (20-30°C) in a vacuum state without additional heating, and the evaporation of the water film does not require a high degree of vacuum. , The negative pressure of 80KPa can maintain fast evaporation and fresh water collection. Therefore, the advantages of seawater desalination technology using ceramic membranes are: energy saving and environmental protection, simple structural devices, easy maintenance, low cost, used ceramic membranes can be washed and recycled, and the obtained fresh water has high purity. In this seawater desalination technology, the evaporation of seawater can be carried out at room temperature, neither expensive reverse osmosis membranes are needed, nor does it need to consume a lot of electricity to heat seawater to boiling point for evaporation.

陶瓷膜的应用三Application of ceramic membrane three

陶瓷膜用作电子产品的导热散热膜时需要陶瓷膜既有优异的电绝缘性,又保持良好的导热性,故需要对陶瓷膜进行相应的处理,所述处理包括如下步骤:首先将陶瓷膜在水玻璃(Na2SiO3·9H2O)溶液中浸渍20–40min,拿出后在100℃度加热烘干20–40min。然后将陶瓷膜在导热树脂溶液中浸渍20–40min,取出在80℃度加热烘干60min。以上处理步骤是将陶瓷膜中的毛细管封起来,增强了陶瓷膜的电绝缘性能和导热性能,本发明中的陶瓷膜是一种新型的导热散热材料,能满足各类电气元件对散热的苛刻要求。When the ceramic film is used as a heat-conducting and heat-dissipating film for electronic products, the ceramic film needs to have both excellent electrical insulation and good thermal conductivity. Therefore, the ceramic film needs to be treated accordingly. The treatment includes the following steps: firstly, the ceramic film Immerse in water glass (Na 2 SiO 3 ·9H 2 O) solution for 20-40min, take it out and heat and dry at 100°C for 20-40min. Then immerse the ceramic film in the thermally conductive resin solution for 20-40 minutes, take it out and heat and dry it at 80°C for 60 minutes. The above processing steps are to seal the capillary in the ceramic film, which enhances the electrical insulation and thermal conductivity of the ceramic film. The ceramic film in the present invention is a new type of heat-conducting and heat-dissipating material, which can meet the requirements of various electrical components for heat dissipation. Require.

本发明尚有多种具体的实施方式,凡采用等同替换或者等效变换而形成的所有技术方案,均落在本发明要求保护的范围之内。The present invention still has many specific implementation modes, and all technical solutions formed by adopting equivalent replacement or equivalent transformation all fall within the protection scope of the present invention.

Claims (7)

1. there is capillary structure and the ceramic membrane of super dehumidifier wetting property, it is characterized in that: described ceramic membrane thickness is 10nm��600 ��m, the base membrane layer that described ceramic membrane comprises an aluminum compound substrate, is attached in described substrate, described base membrane layer is alumina ceramic layer, described ceramic membrane is have the porous-film that average capillary radius is 0.1-1.2mm, described ceramic membrane water-wetted surface can make the water droplet of unit mass spread out completely, forms area and is not less than 300cm2The water film of/g; And water-wetted surface can make water molecules overcome self gravitation, the height of self climbing is not less than 3.0cm in the vertical direction.
2. the preparation method of the ceramic membrane with capillary structure according to claim 1, it is characterised in that: comprise the steps,
S1, substrate pretreatment
S11, substrate degreasing: base material is put into the sulfuric acid tank of 5%��20%, degreasing, take out after 3min��5min; Described base material is aluminium base or aluminum alloy base material;
S12, first time washing: repeatedly rinse aluminium base with tap water, ensure the PH value > 5 on aluminium base surface;
S13, alkali cleaning: the base material after first time washing is put into concentration is 45kg/m3��55kg/m3, temperature is in the sodium hydroxide solution of 40 DEG C��60 DEG C, alkali cleaning 4min��8min;
S14, second time washing: repeatedly rinse aluminium base with tap water, take out after rinsing 2min��4min;
S15, third time washing: repeatedly rinse aluminium base with tap water, rinse 2min��4min, take out after PH value > 5;
S16, anodic oxidation: clean oxidation sequentially with alkaline electrolyte and acid electrolyte, promote that metallic aluminium base material Surface Creation has hole height, the pellumina of high adsorption capacity, and described aluminum oxide film thickness is 0.3��30 ��m;
S17, the 4th washing: repeatedly rinsed by the pellumina tap water through anodic oxidation, rinse and take out after 2min��4min, then with deionized water rinsing 1min��2min;
S18, drying: take out the aluminium base after chemical oxidation, dry after deionized water rinses repeatedly;
S2, alumina ceramic layer coating step;
S21, raw material powder prepare; Carry out Alpha-alumina, organic pore former, sintering aid and other batch ingredients in proportion weighing proportioning: described Alpha-alumina mass percent is 60%-70%, particle diameter is 5-30 ��m, described organic pore former mass percent is 30%-40%, and particle diameter is 3-35 ��m; Described sintering aid mass percent is 10%-30%;
S22, raw material mix: after first Alpha-alumina, organic pore former being mixed, then mix with sintering aid and other batch ingredients: Alpha-alumina and organic pore former are 70-90%, described sintering aid and other batch ingredients is 10-30% mixing;
S23, mixed mill stir: add aluminium oxide ceramic ball or steel ball that 20-30 grain diameter is 5-12mm in mixed powder, mixed mill 1-3h on mixer;
S24, shaping: mixing raw material loads to carry out low-temperature prewarming in mould shaping, described preheating mold temperature is 180-250 DEG C;
S25, intermediate sintering temperature and one-tenth hole; Being proceeded in intermediate sintering temperature stove by product after shaping, be heated to 600 DEG C, the heat-up time of described middle temperature stove is 2-3h, and insulation 1-2h, then cools to less than 100 DEG C with the furnace, finally takes out last obtained porous ceramics from stove.
3. the preparation method of the ceramic membrane with capillary structure and super dehumidifier wetting property according to claim 1, it is characterized in that: in the anodization step of described S16, described electrolytic solution comprises acid electrolyte and alkaline electrolyte, and described acid electrolyte proportioning is: formic acid mass percent 20��40%; Oxalic acid mass percent 30��50%; Propanedioic acid mass percent 30��50%; Single nickel salt mass percent 0��10%, process parameter is: oxidation voltage is 20��80V, and current density is 2.0��3.5A/dm2, and the treatment time is 0.5��3h, and treatment temp is 10��25 DEG C;
Described alkaline electrolyte proportioning is: sodium carbonate mass percent 40��60%; Sodium chromate mass percent 15��25%; Sodium hydroxide mass percent 2��5%; Tertiary sodium phosphate mass percent 0��1.5%, process parameter is: oxidation voltage is 5��35V, and current density is 1.0��2.5A/dm2, and the treatment time is 5��60min, and treatment temp is 85��100 DEG C.
4. the preparation method of the ceramic membrane with capillary structure and super dehumidifier wetting property according to claim 1, it is characterized in that: described S24 low temperature moulding adopts air circulating oven or flattening oven, described air circulating oven preheating mold temperature is 180-250 DEG C, and the low temperature moulding time is 8-12min; Described flattening oven preheating mold temperature is 180-250 DEG C, and the low temperature moulding time is 3-5min.
5. the preparation method of the ceramic membrane with capillary structure and super dehumidifier wetting property according to claim 1, it is characterised in that: the first time washing flush time in described S12 is 2min��4min.
6. the preparation method of the ceramic membrane with capillary structure and super dehumidifier wetting property according to claim 1, it is characterised in that: in described S21, other batch of materials are dispersion solvent.
7. the preparation method of the ceramic membrane with capillary structure and super dehumidifier wetting property according to claim 1, it is characterised in that: described mixer is the mixer of V-structure, and described batch mixing speed is 100-150r/min.
CN201511010377.6A 2015-12-30 2015-12-30 Ceramic membrane with capillary structure and super dehumidifier wetting property and preparation method thereof Expired - Fee Related CN105624759B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201511010377.6A CN105624759B (en) 2015-12-30 2015-12-30 Ceramic membrane with capillary structure and super dehumidifier wetting property and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201511010377.6A CN105624759B (en) 2015-12-30 2015-12-30 Ceramic membrane with capillary structure and super dehumidifier wetting property and preparation method thereof

Publications (2)

Publication Number Publication Date
CN105624759A true CN105624759A (en) 2016-06-01
CN105624759B CN105624759B (en) 2018-02-16

Family

ID=56040091

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201511010377.6A Expired - Fee Related CN105624759B (en) 2015-12-30 2015-12-30 Ceramic membrane with capillary structure and super dehumidifier wetting property and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105624759B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107226719A (en) * 2017-05-12 2017-10-03 华南理工大学 The application of a kind of preparation method of graphene oxide membrane and its graphene oxide membrane of preparation in the dehydration of high concentration ethylene glycol solution

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1004608A (en) * 1961-06-16 1965-09-15 Haeger Potteries Inc Ceramic materials and methods of making same
US4082863A (en) * 1976-09-28 1978-04-04 Hydro-Quebec Fabrication of ceramic heat pipes
CN1411085A (en) * 2001-10-08 2003-04-16 华中科技大学 Proton exchange film and its preparation method
CN1800101A (en) * 2006-01-05 2006-07-12 南京工业大学 Preparation method of porous ceramic material
CN101070212A (en) * 2006-11-15 2007-11-14 天津科技大学 Ceramic-diaphragm sewater pretreating method
CN101445381A (en) * 2008-12-31 2009-06-03 南京航空航天大学 Al core/Al2O-based ceramic sheath self-healing composite foam thermal protection structure simulating capillary plexus and manufacture method thereof
CN102380321A (en) * 2011-09-07 2012-03-21 三达膜科技(厦门)有限公司 Method for preparing coating of alumina ceramic membrane
CN104016708A (en) * 2014-05-29 2014-09-03 西安工程大学 Preparation method of high rupture strength ceramic tube support body
CN104630756A (en) * 2015-01-29 2015-05-20 苏州容电储能科技有限公司 Method for forming high-thermal-conducting hydrophilic nano ceramic film on surface of aluminum

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1004608A (en) * 1961-06-16 1965-09-15 Haeger Potteries Inc Ceramic materials and methods of making same
US4082863A (en) * 1976-09-28 1978-04-04 Hydro-Quebec Fabrication of ceramic heat pipes
CN1411085A (en) * 2001-10-08 2003-04-16 华中科技大学 Proton exchange film and its preparation method
CN1800101A (en) * 2006-01-05 2006-07-12 南京工业大学 Preparation method of porous ceramic material
CN101070212A (en) * 2006-11-15 2007-11-14 天津科技大学 Ceramic-diaphragm sewater pretreating method
CN101445381A (en) * 2008-12-31 2009-06-03 南京航空航天大学 Al core/Al2O-based ceramic sheath self-healing composite foam thermal protection structure simulating capillary plexus and manufacture method thereof
CN102380321A (en) * 2011-09-07 2012-03-21 三达膜科技(厦门)有限公司 Method for preparing coating of alumina ceramic membrane
CN104016708A (en) * 2014-05-29 2014-09-03 西安工程大学 Preparation method of high rupture strength ceramic tube support body
CN104630756A (en) * 2015-01-29 2015-05-20 苏州容电储能科技有限公司 Method for forming high-thermal-conducting hydrophilic nano ceramic film on surface of aluminum

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
夏长荣 等: "γ-Al2O3纳滤膜的结构和透过性能", 《材料研究学报》 *
张红宇: "α-Al203多孔陶瓷无机膜支撑体及涂层研究", 《中北大学硕士学位论文》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107226719A (en) * 2017-05-12 2017-10-03 华南理工大学 The application of a kind of preparation method of graphene oxide membrane and its graphene oxide membrane of preparation in the dehydration of high concentration ethylene glycol solution
CN107226719B (en) * 2017-05-12 2021-01-19 华南理工大学 Preparation method of graphene oxide film and application of graphene oxide film prepared by preparation method in dehydration of high-concentration glycol solution

Also Published As

Publication number Publication date
CN105624759B (en) 2018-02-16

Similar Documents

Publication Publication Date Title
Li et al. Ultrahigh solar steam generation rate of a vertically aligned reduced graphene oxide foam realized by dynamic compression
Wang et al. Superhydrophilic porous carbon foam as a self-desalting monolithic solar steam generation device with high energy efficiency
Wu et al. Highly efficient solar anti-icing/deicing via a hierarchical structured surface
US9103607B2 (en) Porous layer
Hu et al. Carbon nanotubes@ silicone solar evaporators with controllable salt-tolerance for efficient water evaporation in a closed system
CN101643218B (en) A method for synthesizing oriented MFI molecular sieve membranes by microwave heating
Lee et al. Nanoporous anodic alumina oxide layer and its sealing for the enhancement of radiative heat dissipation of aluminum alloy
CN101705488B (en) Surface processing method of super-hydrophobic ice-covering-proof aluminum and steel with rough surface
CN101775586A (en) Preparation method of electrochemical oriented growth of polyporous Al2O3 film on non-aluminum base
CN117209000B (en) An integrated multifunctional solar evaporator and a preparation method thereof
WO2022000608A1 (en) Aerogel composite membrane, preparation method therefor and use thereof
KR20140112848A (en) Fabrication method for hydrophilic aluminum surface and the hydrophilic surface body
CN106784295B (en) A kind of porous metal foam-based IPMC electric actuation material and preparation method thereof
CN105624759B (en) Ceramic membrane with capillary structure and super dehumidifier wetting property and preparation method thereof
CN102631844A (en) Preparation method of hydrophobe polysulfone microporous membrane
Song et al. Efficient anti-icing/deicing via photothermal-wind synergistic effects on femtosecond laser-induced superhydrophobic graphene
Hu et al. Experimental study of nucleate pool boiling heat transfer of self‐rewetting solution by surface functionalization with TiO2 nanostructure
CN106345316B (en) A kind of miillpore filter of acid-resisting corrosion
CN116675896A (en) Phenolic resin sponge material with asymmetric structure and preparation method thereof
CN105695804B (en) Preparation method of high-thermal-conductivity aluminum base graphene composite material
CN117241554A (en) Super-wetting surface-driven liquid drop bouncing type super-heat flux temperature equalizing plate and preparation method thereof
Luo et al. Superlyophilic interfaces assisted thermal management
Deng et al. A skin-effect-inspired 3D solar evaporator for simultaneously achieving highly efficient steam generation and ultra-high salt resistance
CN116239175A (en) Three-dimensional surface plasmon evaporator and preparation method and application thereof
CN101767081A (en) Preparation method of metal-dielectric solar spectrum selective absorption coating

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20180216