Ultrahydrophobic powder, structure with ultrahydrophobic surface, and processes for producing these
A technology of super-hydrophobicity and manufacturing method, which can be used in chemical instruments and methods, papermaking, water repellent addition, etc., and can solve problems such as narrow application range.
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[0133] Hereinafter, the present invention will be further described in detail through examples. In addition, unless otherwise specified, "%" means "mass %".
[0134] [Shape Analysis of Nanofiber Associations and Powders Using a Scanning Electron Microscope]
[0135] The separated and dried aggregates and powders were fixed on the sample support table with double-sided tape, and observed with the surface observation device VE-9800 manufactured by KEYENCE CORPORATION.
[0136] [Observation of Nanostructures Using Transmission Electron Microscopy]
[0137] A sample in a powder state was dispersed in methanol, placed on a copper grid, and observed with a transmission electron microscope "JEM-2200FS" manufactured by JEOL Ltd.
[0138] [Contact angle measurement]
[0139] The contact angle was measured with an automatic contact angle meter Contact Angle System OCA (manufactured by Dataphysics).
[0140] [Differential calorimetry analysis]
[0141] The content of the compound (X...
Synthetic example 1
[0145] [Synthesis of an association of organic-inorganic composite nanofibers (I)]
[0146]Using the method disclosed in the patent literature (Japanese Patent Application Laid-Open No. 2005-264421, Japanese Patent Laid-Open No. 2005-336440, Japanese Patent Laid-Open No. 2006-063097, and Japanese Patent Laid-Open No. 2007-051056) to produce powders with different shapes .
[0147] 5 g of commercially available polyethyloxazoline (number average molecular weight 500,000, average degree of polymerization 5,000, manufactured by Aldrich) was dissolved in 20 mL of 5M aqueous hydrochloric acid. The solution was heated to 90° C. with an oil bath, and stirred at this temperature for 10 hours. 50 mL of acetone was added to the reaction solution to completely precipitate the polymer, which was filtered and washed three times with methanol to obtain white polyethyleneimine powder. The resulting powder is used 1 H-NMR (heavy water) identification, confirmation is derived from the peak ...
Synthetic example 2
[0152] [Synthesis of an association of nanofibers (II) mainly composed of silica]
[0153] 5 g of the powder (I-1) obtained in Synthesis Example 1 was heated in an electric furnace at 600° C. for 2 hours under the condition of introducing air to remove the polyethyleneimine contained in the powder (I-1) to obtain a white powder body (II-1). The specific surface area is 187m 2 / g. figure 2 The SEM photograph of powder (II-1) is shown. It shows that the nanofiber structure does not change after calcination.
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