CN112429966A - Structural member and method of making same - Google Patents

Structural member and method of making same Download PDF

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Publication number
CN112429966A
CN112429966A CN201910790496.XA CN201910790496A CN112429966A CN 112429966 A CN112429966 A CN 112429966A CN 201910790496 A CN201910790496 A CN 201910790496A CN 112429966 A CN112429966 A CN 112429966A
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China
Prior art keywords
glaze
woven cloth
fiber woven
structural member
oxide
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Granted
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CN201910790496.XA
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Chinese (zh)
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CN112429966B (en
Inventor
赵岩峰
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Guangdong Oppo Mobile Telecommunications Corp Ltd
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Guangdong Oppo Mobile Telecommunications Corp Ltd
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    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
    • C04B41/5022—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with vitreous materials
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81—Coating or impregnation
    • C04B41/85—Coating or impregnation with inorganic materials
    • C04B41/86—Glazes; Cold glazes
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/44—Oxides or hydroxides of elements of Groups 2 or 12 of the Periodic Table; Zincates; Cadmates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/45—Oxides or hydroxides of elements of Groups 3 or 13 of the Periodic Table; Aluminates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/73—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof
    • D06M11/76—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof with carbon oxides or carbonates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
    • D06M11/79—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/80—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with boron or compounds thereof, e.g. borides
    • D06M11/82—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with boron or compounds thereof, e.g. borides with boron oxides; with boric, meta- or perboric acids or their salts, e.g. with borax
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P40/00—Technologies relating to the processing of minerals
    • Y02P40/60—Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

The application relates to a structural member and a preparation method thereof, wherein the preparation method of the structural member comprises the following steps: step S110, providing fiber woven cloth; step S120, providing glaze slip; step S130, coating the fiber woven cloth with the glaze slurry, and immersing part of the glaze slurry into the fiber woven cloth to obtain a green body; step S140, sintering and post-processing the green body to obtain a structural member; the structural member comprises a fiber layer and a glaze layer covering the fiber layer, the fiber layer is formed by fiber woven cloth and glaze slurry immersed in the fiber woven cloth, and the glaze layer is formed by the glaze slurry covering the fiber woven cloth. The fiber layer is made by sintering the fiber woven cloth and the glaze slurry immersed in the fiber woven cloth, and the glaze slurry in the fiber woven cloth and the glaze slurry forming the glaze layer are of an integrally formed structure after sintering, so that the structural member has better strength and the glaze layer is not easy to fall off. Compared with the traditional ceramic structural member, the fiber woven cloth has lighter weight, so that the structural member has smaller weight and higher strength.

Description

Structural member and method of making same
Technical Field
The present disclosure relates to the field of electronic devices, and more particularly, to a structural member and a method for manufacturing the same.
Background
The main component of the traditional ceramic structural member is clay, the weight is heavy, and when the ceramic structural member is applied to electronic equipment, the weight of the electronic equipment can be greatly increased, so that heavy hand feeling is brought to users.
Disclosure of Invention
In a first aspect of the present application, an embodiment provides a method for manufacturing a structural member, so as to solve the technical problem of heavy weight of the ceramic structural member.
A method of making a structural member comprising the steps of:
step S110, providing fiber woven cloth;
step S120, providing glaze slip;
step S130, coating the fiber woven cloth with the glaze slurry, and immersing part of the glaze slurry into the fiber woven cloth to obtain a green body; and
step S140, sintering and post-processing the green body to obtain a structural member;
the structural member comprises a fiber layer and a glaze layer covering the fiber layer, the fiber layer is formed by the fiber woven cloth and the glaze slurry immersed in the fiber woven cloth, and the glaze layer is formed by the glaze slurry covering the fiber woven cloth.
The method for preparing the structural member comprises the steps of coating the glaze slurry on the fiber woven cloth, partially immersing the fiber woven cloth in the glaze slurry, and sintering to obtain the structural member, wherein the structural member comprises a fiber layer and a glaze layer covering the fiber layer, and the glaze layer is prepared from the glaze slurry through sintering, so that the structural member has a good decorative effect. The fiber layer is made of fiber woven cloth and glaze slurry immersed in the fiber woven cloth through sintering, and the glaze slurry in the fiber woven cloth and the glaze slurry forming the glaze layer are of an integrally formed structure after sintering, so that the structural member has better strength. Compared with the traditional ceramic structural component, the fiber woven cloth has lighter weight, and the structural component has smaller weight and higher strength under the same size with the traditional ceramic structural component. The glaze layer and the structure formed by sintering the glaze slip in the fiber layer are of an integrally formed structure, so that the glaze layer is not easy to fall off.
In one embodiment, in step S120, a glaze is configured, and a glaze slurry is configured with the glaze.
In one embodiment, the glaze comprises a base material and a pigment, wherein the base material comprises, by mass percentage,
the base material comprises 50-70% of silicon dioxide, 10-20% of aluminum oxide, 5-10% of sodium carbonate, 3-5% of barium carbonate, 2-5% of zirconium oxide and 0-5% of the rest compounds, wherein the rest compounds comprise one or more of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide;
the pigment comprises 5-15% of metal oxide.
In one embodiment, the step of preparing the glaze slip by using the glaze comprises the following steps:
and carrying out ball milling on the glaze and water to obtain glaze slip.
In one embodiment, in step S130, before the step of coating and immersing the glaze slip into the fiber woven cloth to obtain a green body, the method further includes the following steps:
and stretching, fixing and preheating the fiber woven cloth, wherein the preheating temperature is 150-200 ℃, and the preheating time is 10-20 min.
In one embodiment, the step S130 of coating and immersing the glaze slip into the fiber woven cloth to obtain a green body includes:
and coating the glaze slip on the surface of the fiber woven cloth in a spraying manner, wherein the spraying frequency is one time or more, the spraying time of each time is 5-8 s, and the thickness of the glaze slip sprayed on the surface of the fiber woven cloth by each time is 0.1-0.4 mm.
In one embodiment, the step S140, before the step of sintering and post-processing the green body, further includes the steps of:
and drying the green body.
In one embodiment, the post-processing step S140 includes one or more of CNC machining, grinding and coating.
In one embodiment, the woven fiber cloth comprises a woven basalt fiber cloth.
In a second aspect of the present application, an embodiment provides a structural member to solve the above-mentioned technical problem of heavy weight of the ceramic structural member.
The structural part is prepared by the preparation method and comprises a shell or a middle frame or an integrally formed structure of the shell and the middle frame.
In one embodiment, the thickness of the fiber layer is 0.1 mm-0.3 mm, and the thickness of the glaze layer is 0.2 mm-0.3 mm.
Drawings
In order to more clearly illustrate the embodiments of the present application or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, it is obvious that the drawings in the following description are only some embodiments of the present application, and for those skilled in the art, other drawings can be obtained according to the drawings without creative efforts.
Fig. 1 is a perspective view of an electronic device according to an embodiment;
FIG. 2 is a front view of a housing of the electronic device of FIG. 1;
FIG. 3 is a cross-sectional view of the housing shown in FIG. 2;
FIG. 4 is a flow chart illustrating the preparation of the housing according to one embodiment;
FIG. 5 is a flow chart of preparing a glaze slurry according to an embodiment;
FIG. 6 is a flow chart of an embodiment of a method for manufacturing a shell using a fiber woven cloth and a glaze slip;
FIG. 7 is a front view of a woven fabric according to an embodiment;
FIG. 8 is a front view of a green body obtained by coating a fiber woven cloth with an enamel slurry according to an embodiment;
fig. 9 is a cross-sectional view of the green body of fig. 8.
Detailed Description
To facilitate an understanding of the present application, the present application will now be described more fully with reference to the accompanying drawings. Preferred embodiments of the present application are illustrated in the accompanying drawings. This application may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete.
As shown in fig. 1 and 2, in an embodiment, an electronic device 10 is provided, and the electronic device 10 may be a smart phone, a computer, a tablet, a watch, or the like. The electronic device 10 includes a display panel assembly 200, a structural member, a middle frame 300, and a circuit board, and the structural member is described as an example of the housing 100 in this application. It is understood that the structural member may also be a middle frame 300, a key, a camera head decorative ring, a fingerprint decorative ring, etc.; in another embodiment, the structural member may be an integrally formed structure of the middle frame 300 and the shell 100 of an integrally formed fuselage (unibody) structure. The display screen assembly 200 and the housing 100 are respectively fixed on two sides of the middle frame 300, the display screen assembly 200, the middle frame 300 and the housing 100 together form an external structure of the electronic device 10, the circuit board is located inside the electronic device 10, and electronic elements such as a controller, a storage unit, a power management unit, a baseband chip and the like are integrated on the circuit board. The display screen assembly 200 is used to display pictures or fonts, and the circuit board can control the operation of the electronic device 10.
In one embodiment, the Display panel assembly 200 uses an LCD (Liquid Crystal Display) panel for displaying information, and the LCD panel may be a TFT (Thin Film Transistor) screen or an IPS (In-Plane Switching) screen or an SLCD (split Liquid Crystal Display) screen. In another embodiment, the display panel assembly 200 employs an OLED (Organic Light-Emitting display) panel for displaying information, and the OLED panel may be an AMOLED (Active Matrix Organic Light-Emitting Diode) screen or a Super AMOLED (Super Active Matrix Organic Light-Emitting Diode) screen or a Super AMOLED Plus (Super Active Matrix Organic Light-Emitting Diode) screen. Under the control of the controller, the display screen assembly 200 can display information and can provide an operation interface for a user.
As shown in fig. 3, in one embodiment, the shell 100 includes a fiber layer 120 and a glaze layer 110 covering the fiber layer 120. The shell 100 comprises an outer surface 101 and an inner surface 102 which are arranged oppositely, the fiber layer 120 is positioned on one side of the inner surface 102 of the shell 100, and the inner surface 102 is positioned on the fiber layer 120; the glaze layer 110 is located on one side of the outer surface 101 of the casing 100, and the outer surface 101 is located on the glaze layer 110. The fiber layer 120 is made of a fiber woven cloth and glaze slurry infiltrated into the fiber woven cloth by sintering. The glaze layer 110 is made of glaze material covering the fiber woven cloth by sintering. It is understood that the structure formed by sintering glaze slip in the glaze layer 110 and the fiber layer 120 is an integrally formed structure, except that the density of the structure formed by sintering glaze slip in the fiber layer 120 is less than that of the glaze layer 110 due to the fiber woven cloth, but the characteristics of the integrally formed structure are not affected. The structure of the glaze slurry in the fiber layer 120, which is sintered and formed, forms the "cement" of the shell 100 together with the glaze layer 110, and the fiber woven cloth forms the steel bars of the shell 100, so that the shell 100 has better integrity. The glaze layer 110 does not have the fiber woven cloth, so that the surface of the glaze layer 110 is flat and smooth, and the pattern of the glaze layer 110 is not broken by the fibers in the fiber woven cloth, so that the glaze layer 110 has good decoration to the shell 100. When the thickness of the shell 100 is processed, the glaze layer 110 may be ground or polished without breaking the fiber woven cloth.
The fiber woven cloth may be carbon fiber woven cloth, glass fiber woven cloth, basalt fiber woven cloth 130, or the like. In one embodiment, the fiber woven cloth is basalt fiber woven cloth 130, the basalt fiber woven cloth 130 is made of basalt fibers serving as raw materials and is composed of two groups of vertical basalt fibers, the size of the basalt fibers is 7-14 μm, and the length-diameter ratio is 1: 1000-3000. The basalt fiber has good temperature resistance, and the glaze slip can not be burnt or softened, so that the application condition can be met. Warp yarns and weft yarns of the basalt fibers are interwoven together through weaving equipment and a weaving process to be woven into a cloth shape, the thickness of the basalt fiber woven cloth 130 is 0.1 mm-0.3 mm, the tensile strength is 1000 MPa-1400 MPa, such as 1200MPa, and the elastic modulus is 80 GPa-100 GPa, such as 90 GPa. Under the condition of heating at 900 ℃ for 2h, the weight loss of the basalt fiber woven cloth 130 is less than 1%, so that the basalt fiber woven cloth 130 has stable weight in the manufacturing process of the shell 100. It is understood that the thickness of the basalt fiber woven cloth 130 is limited to 0.1mm to 0.3mm according to the needs of the housing 100 of the electronic device 10 to meet the assembly needs of the housing 100 of the electronic device 10. In other embodiments, the thickness of the basalt fiber woven fabric 130 may be in other ranges, such as 0.001mm to 0.1mm, 0.3mm to 1.0mm, 1.0mm to 2.0mm, and the like, and when the thickness of the structural member to be prepared is thick, two or more layers of the basalt fiber woven fabric 130 may be stacked to prepare a structural member with a thick thickness; the basalt fiber woven cloth 130 can also be coated with glaze slip 140 with a relatively thick thickness to produce the glaze layer 110 with a relatively thick thickness.
The glaze layer 110 is made of glaze slip 140 covering the fiber woven cloth by sintering, and the thickness of the glaze layer 110 is 0.2mm to 0.3mm, and in other embodiments, the thickness of the glaze layer 110 may be in other ranges, such as 0.01mm to 0.2mm, 0.3mm to 1.0mm, 1.0mm to 2.0mm, and so on. The glaze slurry 140 is prepared by ball milling glaze and water. The glaze includes a base and a pigment, and the pigment makes the glaze have corresponding colors, thereby obtaining a gorgeous case 100. The base material comprises 50-70% of silicon dioxide (SiO)2) 10% -20% of alumina (Al)2O3) 5 to 10 percent of sodium carbonate (Na)2CO3) 3% -5% of barium carbonate (BaCO)3) 2% -5% of zirconium oxide (ZrO)2) And 0-5% of the balance of compounds, wherein the balance of compounds comprise zinc oxide (ZnO) and cerium oxide (CeO)2) Boric acid (H)3BO3) Potassium oxide (K)2O) and lithium oxide (Li)2O) is used. The pigment comprises 5-15% of metal oxide, and the metal oxide comprises various types of metals which can be Fe, Co, Cr, Cu, Zn, Ti and Al elementsThe oxide may be a metal oxide of other elements, and is not limited herein. The component of the glaze is favorable for having better bonding force with the basalt fiber woven cloth 130, so that the bonding force between the structure after sintering the glaze slurry and the basalt fiber woven cloth 130 and the bonding force between the glaze layer 110 and the basalt fiber woven cloth 130 are increased, the glaze layer 110 and the basalt fiber woven cloth 130 are not easy to separate, the strength of the shell 100 is increased, and the glaze layer 110 also has better decorative effect.
The structural member, such as the shell 100, includes a fiber layer 120 and a glaze layer 110 covering the fiber layer 120, the glaze layer 110 being located on one side of an outer surface 101 of the structural member, and the fiber layer 120 being located on one side of an inner surface 102 of the structural member. The glaze layer 110 is made of the glaze slip 140 through sintering, and can have a good decorative effect on the structural member. The fiber layer 120 is made of fiber woven cloth and glaze slurry dipped into the fiber woven cloth through sintering, the glaze slurry in the fiber woven cloth and the glaze slurry 140 forming the glaze layer 110 are in an integrally formed structure after sintering, which is equivalent to cement in a structural member, and the fiber woven cloth is equivalent to reinforcing steel bars in the structural member, so that the structural member has better strength. Compare with traditional ceramic structure, the fibre is woven the cloth quality and is lighter, and the structure of this application is under same size with traditional ceramic structure, and the structure weight of this application is less, and intensity is higher. Because the bonding force between the structure after the glaze slip sintering in the fiber layer 120 and the fiber woven cloth is stronger, and the bonding force between the glaze layer 110 and the fiber woven cloth is stronger, and the structure after the glaze slip sintering in the fiber layer 120 and the glaze slip sintering in the glaze layer 110 are an integrally formed structure, the glaze layer 110 is not easy to fall off, pinholes are not easy to appear on the surface of the structural member, and the yield of the structural member is higher. The structure of the present application is relatively low in cost, attractive in appearance, light in weight, and high in strength, thereby reducing the overall weight of the electronic device 10.
In one embodiment, as shown in fig. 4, a method for manufacturing a structural member is provided, comprising the steps of:
step S110, providing fiber woven cloth;
step S120, providing glaze slip;
step S130, coating the fiber woven cloth with glaze slurry, and immersing part of the glaze slurry into the fiber woven cloth to obtain a green body 150; and
step S140, sintering and post-processing the green body 150 to obtain a structural member;
the structural member includes a fiber layer 120 and a glaze layer 110 covering the fiber layer 120, the fiber layer 120 is formed of a fiber woven cloth and glaze slurry impregnated into the fiber woven cloth, and the glaze layer 110 is formed of glaze slurry 140 covering the fiber woven cloth.
Step S110, providing fiber woven cloth.
As shown in FIG. 7, in one embodiment, the fiber woven cloth is basalt fiber woven cloth 130, basalt fibers are used as raw materials, the diameter size of the basalt fibers is 7 μm to 14 μm, and the length-diameter ratio is 1:1000 to 3000. Warp yarns and weft yarns are interwoven together by two groups of vertical basalt fibers through weaving equipment and technology to be woven into a cloth shape, and both the warp yarns and the weft yarns are composed of the basalt fibers, but the length extension directions are mutually vertical. The thickness of the basalt fiber braided cloth 130 is 0.1 mm-0.3 mm, the tensile strength is 1000 MPa-1400 MPa, such as 1200MPa, and the elastic modulus is 80 GPa-100 GPa, such as 90 GPa. Under the condition of heating at 900 ℃ for 2h, the weight loss of the basalt fiber woven cloth 130 is less than 1%, so that the basalt fiber woven cloth 130 has stable weight in the manufacturing process of the shell 100.
In other embodiments, the thickness of the basalt fiber woven cloth 130 may be set to other dimensions according to actual needs. When the thickness of the basalt fiber woven cloth 130 to be prepared is thicker, the sizes of the warp and the weft can be increased, namely, the warp and the weft are both composed of more basalt fibers, so that the warp and the weft are thicker, and the thickness of the basalt fiber woven cloth 130 after weaving is thicker; similarly, when the warp and weft are thin, the thickness of the basalt fiber woven cloth 130 after weaving is small.
Step S120, providing glaze slip.
As shown in fig. 5, in one embodiment, the frit is first dispensed. The glaze includes a base and a pigment, and the pigment makes the glaze have corresponding colors, thereby obtaining a gorgeous case 100. The base material comprises 50-70% of silicon dioxide, 10-20% of aluminum oxide, 5-10% of sodium carbonate, 3-5% of barium carbonate, 2-5% of zirconium oxide and 0-5% of the balance compound, wherein the balance compound comprises one or more of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide. The pigment comprises 5-15% of metal oxide, the metal oxide comprises various types, and can be metal oxide of Fe, Co, Cr, Cu, Zn, Ti and Al, and can also be metal oxide of other elements, and the metal oxide is not limited herein. The component of the glaze is favorable for having better bonding force with the basalt fiber woven cloth 130, so that the bonding force between the structure after sintering the glaze slurry and the basalt fiber woven cloth 130 and the bonding force between the glaze layer 110 and the basalt fiber woven cloth 130 are increased, the glaze layer 110 and the basalt fiber woven cloth 130 are not easy to separate, the strength of the shell 100 is increased, and the glaze layer 110 also has better decorative effect.
And secondly, uniformly mixing the glaze, and adding water into the glaze in a planetary ball mill for ball milling to obtain glaze slurry. The ball mill comprises a large ball mill, a middle ball mill and a small ball mill, wherein the diameter ratio of the large ball mill to the middle ball mill to the small ball mill is 2:4: 4. The milling rotation speed of the ball mill is 300 r/min-500 r/min, such as 400r/min, the ball milling time is 1 h-1.5 h, wherein the volume ratio of glaze, the ball mill and water is that the glaze, the ball mill and the water are 1:1.8:0.8, and the glaze slurry after ball milling is sieved by a sieve with 250 meshes or other sizes to obtain finer glaze slurry. It can be understood that the ball mill can be designed with corresponding dimensions according to actual needs, and the rotation speed and the ball milling time of the ball mill and the volume ratio of the glaze, the ball mill and the water can also be designed according to actual needs, which is not limited herein.
Step S130, coating the fiber woven cloth with the glaze slurry, and immersing a part of the glaze slurry into the fiber woven cloth to obtain a green compact 150.
As shown in fig. 6, in an embodiment, the basalt fiber woven cloth 130 is first cleaned with oil stain and placed in a preheating furnace for preheating at a temperature of 150 ℃ to 200 ℃, such as 170 ℃, for a time of 10min to 20min, such as 15 min. And then the basalt fiber woven cloth 130 is stretched and fixed on a fixture and is attached to a profiling 2D or 2.5D or 3D structure, so that the basalt fiber woven cloth 130 is in a 2D or 2.5D or 3D structure without obvious wrinkles.
Next, as shown in fig. 8 and 9, the glaze slip 140 is sprayed on the surface of the basalt fiber woven fabric 130 by spraying to obtain a green compact 150, and the spraying frequency may be one time, two times or more. The time of single spraying is 5 s-8 s, and the thickness of the glaze slip 140 sprayed on the surface of the basalt fiber woven cloth 130 is 0.1 mm-0.4 mm. As shown in fig. 3, the glaze slip 140 naturally levels on the surface of the basalt fiber woven fabric 130, and a part of the glaze slip may be immersed in the gaps of the basalt fiber woven fabric 130 and permeate the basalt fiber woven fabric 130, so as to improve the bonding force between the glaze slip and the basalt fiber woven fabric 130.
Step S140, sintering and post-processing the green compact 150 to obtain a structural member.
The basalt fiber woven fabric 130 covered with the glaze slurry 140, namely the green body 150, is placed in a furnace body for drying, wherein the drying temperature is 60-80 ℃, for example 70 ℃, and the drying time is 50-70 min, for example 60 min. And sintering the dried green body 150 at the sintering temperature of not higher than 900 ℃ for 2-4 h to obtain a crude blank. The rough blank is post-processed to provide the shell 100. The post-processing includes processing hole sites such as a camera hole, and performing processes such as CNC (computerized numerical control) processing, polishing and film coating on the rough blank to obtain the shell 100 with the appearance and the size meeting the requirements.
The present application will be described in detail with reference to examples, but the scope of the present application is not limited thereto.
In the following examples and comparative examples, a drop test was performed on a weight of 180g drop ball, and the bonding force between the glaze layer 110 and the fiber layer 120 was judged according to the drop height and whether the surface glaze layer 110 was dropped.
In the following examples and comparative examples, the case 100 was tested for surface hardness using the Vickers hardness test of GB/T4340.1-2009 metal material.
In the following examples and comparative examples, the number of pinholes was visually judged by visual inspection and the diameter of the pinholes was measured by a microscope. The diameter D of the pinholes with the diameter being more than or equal to 0.05mm and less than 0.1mm, the number N of the pinholes in the whole area being less than or equal to 3 is qualified, and the pinholes with the diameter being less than or equal to 0.05mm can not be observed by naked eyes and can be ignored; the pinhole diameter D > 0.1mm is not acceptable.
Example 1
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is woven by basalt fibers, the diameter of the basalt fibers is 7 mu m, and the length-diameter ratio is 1: 1000; the thickness of the basalt fiber woven cloth 130 is 0.1 mm;
(2) according to the mass percentage, 50% of silicon dioxide, 18% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 4% of the rest compounds are adopted to prepare a base material, wherein the rest compounds comprise one of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing a pigment by adopting 12% of metal oxide, wherein the metal oxide is any one of Fe, Co, Cr, Cu, Zn, Ti and Al; mixing the base material and the pigment to obtain a glaze material;
(3) ball milling glaze and water, wherein the rotational speed of a ball mill is 300r/min, and the ball milling time is 1h, wherein the volume ratio of the glaze to the ball mill to the water is 1:1.8: 0.8; sieving the glaze slip after ball milling through a 250-mesh sieve;
(4) cleaning oil stains on the basalt fiber woven cloth 130, and placing the basalt fiber woven cloth in a preheating furnace for preheating, wherein the preheating temperature is 150 ℃, and the preheating time is 10 min; then fixing the basalt fiber woven cloth 130, spraying the glaze slurry 140 on the surface of the basalt fiber woven cloth 130 to prepare a green blank 150, wherein the spraying frequency is one time, the spraying time is 5s, and the thickness of the sprayed glaze slurry 140 on the surface of the basalt fiber woven cloth 130 is 0.1 mm;
(5) the basalt fiber woven fabric 130 covered with the glaze slurry 140, namely the green body 150, is placed in a furnace body to be dried, the drying temperature is 60 ℃, and the drying time is 50 min. And sintering the dried green body 150 at the sintering temperature of 700 ℃ for 2h to obtain a crude blank, and performing post-treatment on the crude blank to obtain the shell 100 with the size and the shape meeting the requirements. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 2
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, 70% of silicon dioxide, 11% of aluminum oxide, 5.5% of sodium carbonate, 3.5% of barium carbonate, 3% of zirconium oxide and 1% of the rest compounds are used for preparing a base material, wherein the rest compounds comprise one of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing a pigment by adopting 6% of metal oxide, wherein the metal oxide is any one of Fe, Co, Cr, Cu, Zn, Ti and Al; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 3
The preparation process of the case 100 of the present embodiment is as follows:
(1) basalt fiber woven cloth 130 is woven by basalt fibers, the diameter of the basalt fibers is 14 mu m, and the length-diameter ratio is 1: 3000; the thickness of the basalt fiber woven cloth 130 is 0.3 mm;
(2) preparing a base material by adopting 61% of silicon dioxide, 10% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) ball milling glaze and water, wherein the rotational speed of a ball mill is 500r/min, and the ball milling time is 1.5h, wherein the volume ratio of the glaze to the ball mill to the water is 1:1.8: 0.8; sieving the glaze slip after ball milling through a 250-mesh sieve;
(4) cleaning oil stains on the basalt fiber woven cloth 130, and placing the basalt fiber woven cloth in a preheating furnace for preheating, wherein the preheating temperature is 200 ℃, and the preheating time is 20 min; then fixing the basalt fiber woven cloth 130, spraying the glaze slurry 140 on the surface of the basalt fiber woven cloth 130 to prepare a green blank 150, wherein the spraying frequency is one time, the spraying time is 8s, and the thickness of the sprayed glaze slurry 140 on the surface of the basalt fiber woven cloth 130 is 0.4 mm;
(5) the basalt fiber woven fabric 130 covered with the glaze slurry 140, namely the green body 150, is placed in a furnace body to be dried, the drying temperature is 80 ℃, and the drying time is 70 min. And sintering the dried green body 150 at 900 ℃ for 4h to obtain a crude blank, and performing post-treatment on the crude blank to obtain the shell 100 with the size and the shape meeting the requirements. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 4
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 3;
(2) preparing a base material by adopting 54% of silicon dioxide, 20% of aluminum oxide, 7% of sodium carbonate, 4% of barium carbonate, 3% of zirconium oxide and 2% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 3;
(4) a green compact 150 was prepared by the same method as in step (4) of example 3;
(5) the case 100 was prepared by the same method as in step (5) of example 3. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 5
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is woven by basalt fibers, the diameter of the basalt fibers is 10 mu m, and the length-diameter ratio is 1: 2000; the thickness of the basalt fiber woven cloth 130 is 0.2 mm;
(2) preparing a base material by adopting 59% of silicon dioxide, 15% of aluminum oxide, 5% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) ball milling glaze and water, wherein the rotational speed of a ball mill is 400r/min, and the ball milling time is 1.25h, wherein the volume ratio of the glaze to the ball mill to the water is 1:1.8: 0.8; sieving the glaze slip after ball milling through a 250-mesh sieve;
(4) cleaning oil stains on the basalt fiber woven cloth 130, and placing the basalt fiber woven cloth in a preheating furnace for preheating, wherein the preheating temperature is 170 ℃, and the preheating time is 15 min; then fixing the basalt fiber woven cloth 130, spraying the glaze slurry 140 on the surface of the basalt fiber woven cloth 130 to prepare a green blank 150, wherein the spraying frequency is one time, the spraying time is 6.5s, and the thickness of the sprayed glaze slurry 140 on the surface of the basalt fiber woven cloth 130 is 0.25 mm;
(5) the basalt fiber woven fabric 130 covered with the glaze slurry 140, namely the green body 150, is placed in a furnace body to be dried, the drying temperature is 70 ℃, and the drying time is 60 min. And sintering the dried green body 150 at 900 ℃ for 3h to obtain a crude blank, and performing post-treatment on the crude blank to obtain the shell 100 with the size and the shape meeting the requirements. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 6
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 5;
(2) preparing a base material by adopting 56% of silicon dioxide, 15% of aluminum oxide, 10% of sodium carbonate, 4% of barium carbonate, 3% of zirconium oxide and 2% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 5;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 5;
(5) the case 100 was prepared by the same method as in step (5) of example 5. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 7
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by using 57% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 3% of barium carbonate, 4% of zirconium oxide and 3% of the balance compound according to the mass percentage, wherein the balance compound comprises a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 8
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 55% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 5% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 9
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by using 58% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 2% of zirconium oxide and 3% of the balance compound according to the mass percentage, wherein the balance compound comprises a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 10
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 55% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 5% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 11
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, 59 percent of silicon dioxide, 15 percent of alumina, 8 percent of sodium carbonate, 4 percent of barium carbonate and 4 percent of zirconia are adopted; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 12
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 54% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 5% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 13
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 61% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 5% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Example 14
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, preparing a base material by adopting 51 percent of silicon dioxide, 15 percent of alumina, 8 percent of sodium carbonate, 4 percent of barium carbonate, 4 percent of zirconia and 3 percent of the rest compounds, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 15% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 1
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 40% of silicon dioxide, 20% of aluminum oxide, 10% of sodium carbonate, 5% of barium carbonate, 5% of zirconium oxide and 5% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 15% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 2
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 3;
(2) preparing a base material by adopting 64% of silicon dioxide, 7% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 3;
(4) a green compact 150 was prepared by the same method as in step (4) of example 3;
(5) the case 100 was prepared by the same method as in step (5) of example 3. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 3
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 5;
(2) preparing a base material by adopting 62% of silicon dioxide, 15% of aluminum oxide, 2% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 5;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 5;
(5) the case 100 was prepared by the same method as in step (5) of example 5. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 4
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, 60 percent of silicon dioxide, 15 percent of aluminum oxide, 8 percent of sodium carbonate, 4 percent of zirconium oxide and 3 percent of the rest compounds are adopted to prepare a base material, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 5
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, 60 percent of silicon dioxide, 15 percent of aluminum oxide, 8 percent of sodium carbonate, 4 percent of barium carbonate and 3 percent of the rest compounds are adopted to prepare a base material, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 6
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) according to the mass percentage, preparing a base material by adopting 51 percent of silicon dioxide, 15 percent of aluminum oxide, 7 percent of sodium carbonate, 4 percent of barium carbonate, 3 percent of zirconium oxide and 10 percent of the rest compounds, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 10% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
Comparative example 7
The preparation process of the case 100 of the present embodiment is as follows:
(1) the basalt fiber woven cloth 130 is produced by the same method as in the step (1) of example 1;
(2) preparing a base material by adopting 64% of silicon dioxide, 15% of aluminum oxide, 8% of sodium carbonate, 4% of barium carbonate, 4% of zirconium oxide and 3% of the rest compounds according to the mass percentage, wherein the rest compounds comprise a plurality of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide; preparing pigment by adopting 2% of metal oxide, wherein the metal oxide is metal oxide of multiple elements in Fe, Co, Cr, Cu, Zn, Ti and Al elements; mixing the base material and the pigment to obtain a glaze material;
(3) preparing glaze slip by the same method as the step (3) of the example 1;
(4) a green compact 150 was prepared in the same manner as in the step (4) of example 1;
(5) the case 100 is prepared by the same method as in the step (5) of example 1. The bonding force, surface hardness and pinhole condition of the case 100 are listed in table 1.
TABLE 1
Figure BDA0002179401070000191
Figure BDA0002179401070000201
Figure BDA0002179401070000211
The results in table 1 show that the cases 100 of examples 1 to 14 have higher bonding force, stronger surface hardness and qualified pinhole conditions, so that the cases 100 with better mechanical properties and better surface quality are obtained.
Example 1, example 2 and comparativeExample 1 comparison shows that Silica (SiO)2) When the mass percentage of the glaze layer 110 to the fiber layer 120 is 50 to 70 percent, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100 and qualified pinhole condition, i.e. good surface quality of the shell 100.
As can be seen by comparing examples 3 and 4 with comparative example 2, alumina (Al)2O3) When the mass percentage of the glaze layer 110 to the fiber layer 120 is 10 to 20 percent, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100 and qualified pinhole condition, i.e. good surface quality of the shell 100.
As can be seen by comparing examples 5 and 6 with comparative example 3, sodium carbonate (Na)2CO3) When the mass percentage of the glaze layer 110 to the fiber layer 120 is 5 to 10 percent, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100 and qualified pinhole condition, i.e. good surface quality of the shell 100.
As can be seen by comparing examples 7 and 8 with comparative example 4, barium carbonate (BaCO)3) When the mass percentage of the glaze layer 110 to the fiber layer 120 is 3 to 5 percent, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100 and qualified pinhole condition, i.e. good surface quality of the shell 100.
As can be seen by comparing examples 9 and 10 with comparative example 5, zirconia (ZrO)2) When the mass percentage of the glaze layer 110 to the fiber layer 120 is 2 to 5 percent, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100 and qualified pinhole condition, i.e. good surface quality of the shell 100.
Comparing examples 11 and 12 with comparative example 6, it can be seen that when the mass percentage of the remaining compound is 0-5%, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100, and qualified pinhole condition, i.e., good surface quality of the shell 100.
Comparing examples 13 and 14 with comparative example 7, it can be seen that when the mass percentage of the metal oxide is 5-15%, the prepared shell 100 has good bonding force between the glaze layer 110 and the fiber layer 120, high surface hardness of the shell 100, and qualified pinhole condition, i.e. good surface quality of the shell 100.
The technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.
The above-mentioned embodiments only express several embodiments of the present application, and the description thereof is more specific and detailed, but not construed as limiting the claims. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the concept of the present application, which falls within the scope of protection of the present application. Therefore, the protection scope of the present patent shall be subject to the appended claims.

Claims (11)

1. A method for manufacturing a structural member, comprising the steps of:
step S110, providing fiber woven cloth;
step S120, providing glaze slip;
step S130, coating the fiber woven cloth with the glaze slurry, and immersing part of the glaze slurry into the fiber woven cloth to obtain a green body; and
step S140, sintering and post-processing the green body to obtain a structural member;
the structural member comprises a fiber layer and a glaze layer covering the fiber layer, the fiber layer is formed by the fiber woven cloth and the glaze slurry immersed in the fiber woven cloth, and the glaze layer is formed by the glaze slurry covering the fiber woven cloth.
2. The method for manufacturing a structural member according to claim 1, wherein in step S120, a glaze is provided, and glaze slurry is provided using the glaze.
3. The method for producing a structural member according to claim 2, wherein the glaze comprises a binder and a pigment, in terms of mass percentage,
the base material comprises 50-70% of silicon dioxide, 10-20% of aluminum oxide, 5-10% of sodium carbonate, 3-5% of barium carbonate, 2-5% of zirconium oxide and 0-5% of the rest compounds, wherein the rest compounds comprise one or more of zinc oxide, cerium oxide, boric acid, potassium oxide and lithium oxide;
the pigment comprises 5-15% of metal oxide.
4. The method for manufacturing a structural element according to claim 2, wherein said step of preparing a slip using said glaze comprises:
and carrying out ball milling on the glaze and water to obtain glaze slip.
5. The method for preparing a structural member according to claim 1, wherein the step S130 further comprises the following steps before the step of coating and dipping the glaze slurry into the fiber woven cloth to obtain a green body:
and stretching, fixing and preheating the fiber woven cloth, wherein the preheating temperature is 150-200 ℃, and the preheating time is 10-20 min.
6. The method for preparing the structural member according to claim 1, wherein the step of coating and dipping the glaze slurry into the fiber woven cloth to obtain a green body in the step S130 comprises:
and coating the glaze slip on the surface of the fiber woven cloth in a spraying manner, wherein the spraying frequency is one time or more, the spraying time of each time is 5-8 s, and the thickness of the glaze slip sprayed on the surface of the fiber woven cloth by each time is 0.1-0.4 mm.
7. The method of manufacturing a structural member according to claim 1, wherein the step of sintering and post-treating the green body in step S140 further comprises the steps of:
and drying the green body.
8. The method of claim 1, wherein the post-processing in step S140 comprises one or more of CNC machining, grinding and coating.
9. The method of making a structural member according to claim 1 wherein said woven fabric comprises a woven basalt fabric.
10. A structural member, characterized in that the structural member is prepared by the method for preparing the structural member according to any one of claims 1 to 9, and the structural member comprises a shell or a middle frame or an integrally formed structure of the shell and the middle frame.
11. The structural member of claim 10, wherein the fibrous layer has a thickness of 0.1mm to 0.3mm and the enamel layer has a thickness of 0.2mm to 0.3 mm.
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CH233125A (en) * 1940-07-16 1944-07-15 Degussa Glaze for ceramic objects.
GB1281153A (en) * 1969-07-19 1972-07-12 Reimbold & Strick Glaze coating
GB1426219A (en) * 1972-11-03 1976-02-25 Commerical Decal Inc Ceramic decalcomania and method of making it
CN85109226A (en) * 1984-11-28 1986-07-02 格哈特·罗索里厄斯 Improve the method for textile properties
EP0539942A1 (en) * 1991-10-28 1993-05-05 J. Hardoncourt Trepagnier Loop pile fabric
EP1271726A2 (en) * 2001-06-26 2003-01-02 Ngk Spark Plug Co., Ltd Method for producing spark plug
JP2004010428A (en) * 2002-06-07 2004-01-15 Toto Ltd Method for producing sanitary earthenware
CN103287008A (en) * 2012-02-23 2013-09-11 深圳富泰宏精密工业有限公司 Coated element and preparation method thereof
CN108570859A (en) * 2018-04-20 2018-09-25 苏州宏久航空防热材料科技有限公司 A kind of corrosion-and high-temp-resistant glass fabric
CN112174696A (en) * 2019-07-02 2021-01-05 Oppo广东移动通信有限公司 Ceramic structural member, glaze for surface decoration of ceramic structural member, preparation method of ceramic structural member and electronic equipment

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH233125A (en) * 1940-07-16 1944-07-15 Degussa Glaze for ceramic objects.
GB1281153A (en) * 1969-07-19 1972-07-12 Reimbold & Strick Glaze coating
GB1426219A (en) * 1972-11-03 1976-02-25 Commerical Decal Inc Ceramic decalcomania and method of making it
CN85109226A (en) * 1984-11-28 1986-07-02 格哈特·罗索里厄斯 Improve the method for textile properties
EP0539942A1 (en) * 1991-10-28 1993-05-05 J. Hardoncourt Trepagnier Loop pile fabric
EP1271726A2 (en) * 2001-06-26 2003-01-02 Ngk Spark Plug Co., Ltd Method for producing spark plug
JP2004010428A (en) * 2002-06-07 2004-01-15 Toto Ltd Method for producing sanitary earthenware
CN103287008A (en) * 2012-02-23 2013-09-11 深圳富泰宏精密工业有限公司 Coated element and preparation method thereof
CN108570859A (en) * 2018-04-20 2018-09-25 苏州宏久航空防热材料科技有限公司 A kind of corrosion-and high-temp-resistant glass fabric
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