CN110467442A - A kind of high-strength porcelain insulator and preparation method thereof - Google Patents
A kind of high-strength porcelain insulator and preparation method thereof Download PDFInfo
- Publication number
- CN110467442A CN110467442A CN201910860422.9A CN201910860422A CN110467442A CN 110467442 A CN110467442 A CN 110467442A CN 201910860422 A CN201910860422 A CN 201910860422A CN 110467442 A CN110467442 A CN 110467442A
- Authority
- CN
- China
- Prior art keywords
- solution
- solid phase
- parts
- porcelain insulator
- preparation
- 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
Links
Classifications
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
-
- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B17/00—Insulators or insulating bodies characterised by their form
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B19/00—Apparatus or processes specially adapted for manufacturing insulators or insulating bodies
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3201—Alkali metal oxides or oxide-forming salts thereof
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3224—Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
- C04B2235/3229—Cerium oxides or oxide-forming salts thereof
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3231—Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3232—Titanium oxides or titanates, e.g. rutile or anatase
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3231—Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3251—Niobium oxides, niobates, tantalum oxides, tantalates, or oxide-forming salts thereof
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3293—Tin oxides, stannates or oxide forming salts thereof, e.g. indium tin oxide [ITO]
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3409—Boron oxide, borates, boric acids, or oxide forming salts thereof, e.g. borax
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
- C04B2235/3472—Alkali metal alumino-silicates other than clay, e.g. spodumene, alkali feldspars such as albite or orthoclase, micas such as muscovite, zeolites such as natrolite
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/349—Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
- C04B2235/6567—Treatment time
-
- 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
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
The invention discloses a kind of high-strength porcelain insulator and preparation method thereof, the porcelain insulator is sintered by following raw materials according: 8~16 parts of kaolin, 9~20 parts of quartz sand, 10~14 parts of mullite, 2~5 parts of potassium feldspar, 2~5 parts of titanium dioxide additive, 40~50 parts of bauxite and 6~20 parts of nano boric acid cerium.The beneficial effects of the present invention are, the present invention changes the component and proportion of porcelain insulator raw material on the basis of conventional preparation techniques, porcelain insulator obtained compared with the prior art in porcelain insulator have more excellent tensile strength and compression strength, and good insulating properties is maintained, the erection suitable for UHV transmission line is installed.
Description
Technical field
The invention belongs to insulator technology fields more particularly to a kind of high-strength porcelain insulator and preparation method thereof.
Background technique
UHV transmission line transmission capacity is big, and the conductor cross-section of use is big, and branch's number is more, to the exhausted of carrying wire tension
More stringent requirements are proposed for edge, it is desirable that its bearing capacity is high, uniform force.It is general to can solve this problem there are two types of mode,
First is that increasing insulator serial number, second is that using the insulator of high mechanical strength.Increasing insulator serial number will lead to insulator
Hardware string complicated in mechanical structure, installation and operation maintenance workload is big, increase engineering overall life cycle cost;And it uses mechanical strong
Insulator serial number can be reduced by spending higher insulator, reduce strain hardware fitting string complexity, reduce operation expense.
Summary of the invention
In order to solve the above technical problems, the porcelain insulator is by following the present invention provides a kind of high-strength porcelain insulator
Raw material is sintered: kaolin, quartz sand, mullite, potassium feldspar, titanium dioxide additive, bauxite and nano boric acid cerium;
The preparation method of the titanium dioxide additive comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh or more, collects powder after sieving, mistake
Powder acetone washing after sieve, drying obtain solid phase A;
2) mixture being formed in the ammonia spirit containing ethylene glycol in solid phase A immersion, mixture is placed in closed container,
Container is sealed, 150~170 DEG C of 10~30min of heat preservation are heated to, then naturally cools to room temperature, closed container is opened and takes out
Mixture is separated by solid-liquid separation, and solid phase is washed with deionized 2~3 times, is dried, and solid phase B is obtained;
3) the solid phase B is immersed in silicon tetrachloride, to solution vacuumize process until not having bubble to emerge, solution is taken
Out, be separated by solid-liquid separation, solid phase drying obtain solid phase C, solid phase C is placed under nitrogen protection atmosphere be heated to 200 DEG C heat preservation 20~
30min is then proceeded to be warming up to 400~500 DEG C of 1~2h of heat preservation, is air-cooled to room temperature after heat preservation, obtains the titanium dioxide
Additive.
Further, each raw material mixing quality portion rate are as follows: 8~16 parts of kaolin, 9~20 parts of quartz sand, mullite 10
~14 parts, 2~5 parts of potassium feldspar, 2~5 parts of titanium dioxide additive, 40~50 parts of bauxite and 6~20 parts of nano boric acid cerium.
Further, in the ammonia spirit containing ethylene glycol, NH3Mass percentage be 5%~10%, ethylene glycol
Volume fraction is 1%~3%, and the ammonia spirit quality containing ethylene glycol is 5 times or more for impregnating solid phase A mass therein.
Further, the silicon tetrachloride quality is 5 times or more for impregnating solid phase A mass therein.
Further, the nano boric acid cerium the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, solution A constant temperature water bath is to 50~60 DEG C, Xiang Rong
Oleic acid is added in liquid A, is stirred solution 40min or more;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 2~3 times, drying obtains the nano boric acid cerium.
Further, Na in the solution A2B4O7·10H2The concentration of O is 3~5g/100mL, remaining is water;In solution B
The concentration of cerous nitrate is 1~4g/mL, remaining is water;Amount=8~10g/100mL of the oleic acid additional amount/solution A.
The invention also discloses the preparation methods of above-mentioned high-strength porcelain insulator, comprise the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18% (all water content of the present invention refer both to aqueous mass percentage), the aging 48h or more of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the mud cake after stirring is aging, and sprayed to mud cake
The aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjusting mud cake water content is 20%~25%, extrusion molding, 120 DEG C
It is dried below to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 420~500 DEG C of first segment keep the temperature 5~7 hours, 980~1000 DEG C of second segment
1~2h is kept the temperature, 1150~1200 DEG C of third section keep the temperature 5~7 hours, furnace cooling after roasting, mucilage binding, test, and finished product enters
Library obtains the high-strength porcelain insulator.
Further, in the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, the mass percentage of each component
For polyethylene glycol 10%~16%, stannic chloride 5%~8%, tantalic chloride 2%~3%.
As can be seen from the above technical solutions, the beneficial effects of the present invention are base of the present invention in conventional preparation techniques
Change the component and proportion of porcelain insulator raw material on plinth, porcelain insulator obtained compared with the prior art in porcelain insulator tool
There are more excellent tensile strength and compression strength, and maintains good insulating properties, the frame suitable for UHV transmission line
If installation.
Specific embodiment
It is described in detail below with reference to embodiment:
Embodiment 1
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 8 parts of kaolin, 9 parts of quartz sand, not
Come 10 parts of stone, 2 parts of potassium feldspar, 2 parts of titanium dioxide additive, 40 parts of bauxite and 6 parts of nano boric acid cerium.
The preparation method of titanium dioxide additive described in the present embodiment comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 5%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 1%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
10min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 20min, then proceed to be warming up to 400 DEG C of heat preservation 2h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
Nano boric acid cerium described in the present embodiment the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 3g/100mL, remaining is water;The concentration of cerous nitrate is 1g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=8g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in the present embodiment, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 10%, stannic chloride 5%, tantalic chloride 2%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 420~430 DEG C of first segment keep the temperature 5 hours, 980~1000 DEG C of second segment guarantors
1~2h of temperature, 1150~1200 DEG C of third section keep the temperature 5~7 hours, furnace cooling after roasting, mucilage binding, test, warehousing finished products,
Obtain the high-strength porcelain insulator.
Embodiment 2
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 10 parts of kaolin, 12 parts of quartz sand,
11 parts of mullite, 3 parts of potassium feldspar, 3 parts of titanium dioxide additive, 43 parts of bauxite and 10 parts of nano boric acid cerium.
The preparation method of titanium dioxide additive described in the present embodiment comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 7%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 2%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
20min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 20min, then proceed to be warming up to 430 DEG C of heat preservation 2h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
Nano boric acid cerium described in the present embodiment the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 4g/100mL, remaining is water;The concentration of cerous nitrate is 2g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=9g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in the present embodiment, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 12%, stannic chloride 6%, tantalic chloride 2%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 440~450 DEG C of first segment keep the temperature 6 hours, 980~1000 DEG C of second segment guarantors
Warm 1h, 1150~1200 DEG C of third section keep the temperature 6 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Embodiment 3
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 14 parts of kaolin, 16 parts of quartz sand,
13 parts of mullite, 4 parts of potassium feldspar, 4 parts of titanium dioxide additive, 48 parts of bauxite and 12 parts of nano boric acid cerium.
The preparation method of titanium dioxide additive described in the present embodiment comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 8%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 2%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
20min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 30min, then proceed to be warming up to 480 DEG C of heat preservation 1h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
Nano boric acid cerium described in the present embodiment the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 4g/100mL, remaining is water;The concentration of cerous nitrate is 3g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=9g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in the present embodiment, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 14%, stannic chloride 7%, tantalic chloride 3%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 460~470 DEG C of first segment keep the temperature 6 hours, 980~1000 DEG C of second segment guarantors
Warm 2h, 1150~1200 DEG C of third section keep the temperature 6 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Embodiment 4
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 16 parts of kaolin, 20 parts of quartz sand,
14 parts of mullite, 5 parts of potassium feldspar, 5 parts of titanium dioxide additive, 50 parts of bauxite and 20 parts of nano boric acid cerium.
The preparation method of titanium dioxide additive described in the present embodiment comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 10%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 3%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
30min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 30min, then proceed to be warming up to 500 DEG C of heat preservation 1h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
Nano boric acid cerium described in the present embodiment the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 5g/100mL, remaining is water;The concentration of cerous nitrate is 4g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=10g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in the present embodiment, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 16%, stannic chloride 8%, tantalic chloride 3%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 480~500 DEG C of first segment keep the temperature 7 hours, 980~1000 DEG C of second segment guarantors
Warm 2h, 1150~1200 DEG C of third section keep the temperature 7 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Comparative example 1
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 14 parts of kaolin, 16 parts of quartz sand,
13 parts of mullite, 4 parts of potassium feldspar, 4 parts of titania powder, 48 parts of bauxite and 12 parts of nano boric acid cerium.
The preparation method of titania powder described in this comparative example comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying, obtains the titania powder.
Nano boric acid cerium described in this comparative example the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 4g/100mL, remaining is water;The concentration of cerous nitrate is 3g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=9g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in the present embodiment, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 14%, stannic chloride 7%, tantalic chloride 3%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 460~470 DEG C of first segment keep the temperature 6 hours, 980~1000 DEG C of second segment guarantors
Warm 2h, 1150~1200 DEG C of third section keep the temperature 6 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Comparative example 2
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 14 parts of kaolin, 16 parts of quartz sand,
13 parts of mullite, 4 parts of potassium feldspar, 4 parts of titanium dioxide additive and 48 parts of bauxite.
The preparation method of titanium dioxide additive described in this comparative example comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 8%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 2%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
20min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 30min, then proceed to be warming up to 480 DEG C of heat preservation 1h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
The preparation method of high-strength porcelain insulator described in this comparative example, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the polyethylene glycol, stannic chloride and tantalic chloride
Aqueous solution in, the mass percentage of each component is polyethylene glycol 14%, stannic chloride 7%, tantalic chloride 3%;Stir it is aging after
Mud cake, and spray to mud cake the aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjust mud cake water content be 20%~
25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 460~470 DEG C of first segment keep the temperature 6 hours, 980~1000 DEG C of second segment guarantors
Warm 2h, 1150~1200 DEG C of third section keep the temperature 6 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Comparative example 3
A kind of high-strength porcelain insulator, the porcelain insulator are sintered by following raw materials according: 14 parts of kaolin, 16 parts of quartz sand,
13 parts of mullite, 4 parts of potassium feldspar, 4 parts of titanium dioxide additive, 48 parts of bauxite and 12 parts of nano boric acid cerium.
The preparation method of titanium dioxide additive described in this comparative example comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh, powder after sieving is collected, after sieving
Powder acetone washing, drying obtain solid phase A;
2) NH is configured3Mass percentage be 8%, the ammonia spirit containing ethylene glycol that the volume fraction of ethylene glycol is 2%, will
Mixture, the ammonia spirit quality containing ethylene glycol in mixture are formed in the ammonia spirit containing ethylene glycol in the solid phase A immersion
For 5 times for impregnating solid phase A mass therein;Mixture is placed in closed container, container is sealed, is heated to 160 ± 10 DEG C
20min is kept the temperature, room temperature is then naturally cooled to, closed container is opened and takes out mixture, be separated by solid-liquid separation, solid phase is washed with deionized water
It washs 3 times, dries, obtain solid phase B;
3) the solid phase B is immersed in silicon tetrachloride, silicon tetrachloride quality is 5 times for impregnating solid phase A mass therein, right
Solution vacuumize process takes out solution until not having bubble to emerge, and is separated by solid-liquid separation, and solid phase drying obtains solid phase C, by solid phase C
It is placed under nitrogen protection atmosphere and is heated to 200 DEG C of heat preservation 30min, then proceed to be warming up to 480 DEG C of heat preservation 1h, it is empty after heat preservation
It is cooled to room temperature, obtains the titanium dioxide additive.
Nano boric acid cerium described in this comparative example the preparation method comprises the following steps:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, Na in the solution A2B4O7·10H2O's is dense
Degree is 4g/100mL, remaining is water;The concentration of cerous nitrate is 3g/mL in solution B, remaining is water;Solution A constant temperature water bath to 50~
60 DEG C, oleic acid is added into solution A, oleic acid additional amount/solution A amount=9g/100mL is stirred solution 40min;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 3 times, drying obtains the nano boric acid cerium.
The preparation method of high-strength porcelain insulator described in this comparative example, comprises the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h of mud cake;
Step 2, with deionized water adjust mud cake water content be 20%~25%, extrusion molding, 100 ± 5 DEG C of dryings to water content 12%
~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 460~470 DEG C of first segment keep the temperature 6 hours, 980~1000 DEG C of second segment guarantors
Warm 2h, 1150~1200 DEG C of third section keep the temperature 6 hours, furnace cooling after roasting, mucilage binding, test, and warehousing finished products obtain institute
State high-strength porcelain insulator.
Embodiment 5
Test sample is prepared according to method described in Examples 1 to 4 and comparative example 1~3, tests the tension of same group of sample respectively
Intensity and compression strength, the results are shown in Table 1.
Table 1
Test group | Tensile strength/MPa | Compression strength/MPa |
Embodiment 1 | 224.25 | 2884.32 |
Embodiment 2 | 231.08 | 2899.51 |
Embodiment 3 | 233.51 | 2967.74 |
Embodiment 4 | 229.86 | 2893.38 |
Comparative example 1 | 168.80 | 1520.05 |
Comparative example 2 | 85.01 | 632.58 |
Comparative example 3 | 144.43 | 1398.22 |
As shown in Table 1, using the titanium dioxide additive and nano boric acid cerium of preparation method of the present invention preparation as raw material
Porcelain insulator obtained has more excellent tensile strength and compression strength compared to currently used porcelain insulator;Comparison is real
Apply example 3 and comparative example 3 it is found that in porcelain insulator preparation process be added polyethylene glycol, stannic chloride and tantalic chloride aqueous solution,
The mechanical property of insulator product can be further increased, improves strengths in tension and compression, this may be due to inside porcelain insulator
The result that micro-crack is partially made up.
Technical solution provided by the present invention is described in detail above, for those of ordinary skill in the art,
Thought according to an embodiment of the present invention, there will be changes in the specific implementation manner and application range, in conclusion this theory
Bright book content should not be construed as limiting the invention.
Claims (8)
1. a kind of high-strength porcelain insulator, which is characterized in that the porcelain insulator is sintered by following raw materials according: kaolin, stone
Sand, mullite, potassium feldspar, titanium dioxide additive, bauxite and nano boric acid cerium;
The preparation method of the titanium dioxide additive comprises the following steps:
1) titania powder is subjected to ball milling, the powder after ball milling crosses the sieve of 1500 mesh or more, collects powder after sieving, mistake
Powder acetone washing after sieve, drying obtain solid phase A;
2) mixture being formed in the ammonia spirit containing ethylene glycol in solid phase A immersion, mixture is placed in closed container,
Container is sealed, 150~170 DEG C of 10~30min of heat preservation are heated to, then naturally cools to room temperature, closed container is opened and takes out
Mixture is separated by solid-liquid separation, and solid phase is washed with deionized 2~3 times, is dried, and solid phase B is obtained;
3) the solid phase B is immersed in silicon tetrachloride, to solution vacuumize process until not having bubble to emerge, solution is taken
Out, be separated by solid-liquid separation, solid phase drying obtain solid phase C, solid phase C is placed under nitrogen protection atmosphere be heated to 200 DEG C heat preservation 20~
30min is then proceeded to be warming up to 400~500 DEG C of 1~2h of heat preservation, is air-cooled to room temperature after heat preservation, obtains the titanium dioxide
Additive.
2. a kind of high-strength porcelain insulator according to claim 1, which is characterized in that each raw material mixing quality portion rate
Are as follows: 8~16 parts of kaolin, 9~20 parts of quartz sand, 10~14 parts of mullite, 2~5 parts of potassium feldspar, titanium dioxide additive 2~5
Part, 40~50 parts of bauxite and 6~20 parts of nano boric acid cerium.
3. a kind of high-strength porcelain insulator according to claim 1, which is characterized in that the ammonia spirit containing ethylene glycol
In, NH3Mass percentage be 5%~10%, the volume fraction of ethylene glycol is 1%~3%, the ammonia spirit quality containing ethylene glycol
For 5 times or more for impregnating solid phase A mass therein.
4. a kind of high-strength porcelain insulator according to claim 1, which is characterized in that the silicon tetrachloride quality is to impregnate
5 times or more of solid phase A mass therein.
5. a kind of high-strength porcelain insulator according to claim 1, which is characterized in that the preparation side of the nano boric acid cerium
Method are as follows:
(1) Na is configured2B4O7·10H2The water solution A and cerous nitrate solution B of O, solution A constant temperature water bath is to 50~60 DEG C, to solution
Oleic acid is added in A, is stirred solution 40min or more;
(2) after the completion of stirring, solution B is added dropwise into solution A under stirring, until no longer generating precipitating, is added dropwise
It filters after the completion, for solid phase with ethanol washing 2~3 times, drying obtains the nano boric acid cerium.
6. a kind of high-strength porcelain insulator according to claim 5, which is characterized in that Na in the solution A2B4O7·
10H2The concentration of O is 3~5g/100mL, remaining is water;The concentration of cerous nitrate is 1~4g/mL in solution B, remaining is water;It is described
Oleic acid additional amount/solution A amount=8~10g/100mL.
7. the preparation method of high-strength porcelain insulator as claimed in claim 2, which is characterized in that comprise the following steps:
Step 1 weighs each raw material by the mass fraction, and each raw material is mixed, sieving, mud refining, and mud cake water content holding 12%~
18%, the aging 48h or more of mud cake;
Step 2, the aqueous solution for configuring polyethylene glycol, stannic chloride and tantalic chloride, the mud cake after stirring is aging, and sprayed to mud cake
The aqueous solution of the polyethylene glycol, stannic chloride and tantalic chloride, adjusting mud cake water content is 20%~25%, extrusion molding, 120 DEG C
It is dried below to water content 12%~18%, repaired biscuit, glazing;
Step 3, blank are roasted with three sections of oxidizing flame, and 420~500 DEG C of first segment keep the temperature 5~7 hours, 980~1000 DEG C of second segment
1~2h is kept the temperature, 1150~1200 DEG C of third section keep the temperature 5~7 hours, furnace cooling after roasting, mucilage binding, test, and finished product enters
Library obtains the high-strength porcelain insulator.
8. preparation method as claimed in claim 7, which is characterized in that the water of the polyethylene glycol, stannic chloride and tantalic chloride
In solution, the mass percentage of each component is polyethylene glycol 10%~16%, stannic chloride 5%~8%, tantalic chloride 2%~3%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910860422.9A CN110467442B (en) | 2019-09-11 | 2019-09-11 | High-strength porcelain insulator and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910860422.9A CN110467442B (en) | 2019-09-11 | 2019-09-11 | High-strength porcelain insulator and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN110467442A true CN110467442A (en) | 2019-11-19 |
CN110467442B CN110467442B (en) | 2021-12-28 |
Family
ID=68515617
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910860422.9A Active CN110467442B (en) | 2019-09-11 | 2019-09-11 | High-strength porcelain insulator and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110467442B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110922157A (en) * | 2019-12-18 | 2020-03-27 | 江西省萍乡市南坑高压电瓷有限公司 | Electroceramic blank and manufacturing method thereof |
CN111099882A (en) * | 2019-12-30 | 2020-05-05 | 湖南高强电瓷电器有限公司 | High-strength ultrahigh-voltage hollow porcelain insulator and preparation method thereof |
CN112919882A (en) * | 2021-03-30 | 2021-06-08 | 江西省萍乡市华东出口电瓷有限公司 | High-strength high-hardness weather-resistant porcelain insulator and preparation method thereof |
CN113402932A (en) * | 2021-07-01 | 2021-09-17 | 江西东维电气有限公司 | Self-cleaning type high strength clavate porcelain insulator |
CN115974534A (en) * | 2023-02-07 | 2023-04-18 | 江西省萍乡市华东出口电瓷有限公司 | Suspension porcelain insulator with aluminum oxide cylindrical head structure |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4983556A (en) * | 1987-03-06 | 1991-01-08 | Ngk Insulators, Ltd. | High strength porcelains for use in insulators and production thereof |
JP2001048672A (en) * | 1999-07-12 | 2001-02-20 | Res Inst Of Natl Defence | Low density and high strength heat-insulating material and its production |
CN103426572A (en) * | 2012-05-21 | 2013-12-04 | 韩国电气安全公社 | Method for manufacturing polymer insulator and insulator manufactured by the method |
CN104987044A (en) * | 2015-07-20 | 2015-10-21 | 湖南稀土金属材料研究院 | High-strength aluminous electroceramics and preparation method thereof |
CN105254280A (en) * | 2015-11-13 | 2016-01-20 | 湖南大学 | Preparation method of high-strength electroceramic |
CN107954704A (en) * | 2017-12-13 | 2018-04-24 | 谢琦 | A kind of porcelain insulator and preparation method thereof |
CN108395225A (en) * | 2018-04-11 | 2018-08-14 | 佛山市拓拓网络科技有限公司 | A kind of electronic ceramics |
-
2019
- 2019-09-11 CN CN201910860422.9A patent/CN110467442B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4983556A (en) * | 1987-03-06 | 1991-01-08 | Ngk Insulators, Ltd. | High strength porcelains for use in insulators and production thereof |
JP2001048672A (en) * | 1999-07-12 | 2001-02-20 | Res Inst Of Natl Defence | Low density and high strength heat-insulating material and its production |
CN103426572A (en) * | 2012-05-21 | 2013-12-04 | 韩国电气安全公社 | Method for manufacturing polymer insulator and insulator manufactured by the method |
CN104987044A (en) * | 2015-07-20 | 2015-10-21 | 湖南稀土金属材料研究院 | High-strength aluminous electroceramics and preparation method thereof |
CN105254280A (en) * | 2015-11-13 | 2016-01-20 | 湖南大学 | Preparation method of high-strength electroceramic |
CN107954704A (en) * | 2017-12-13 | 2018-04-24 | 谢琦 | A kind of porcelain insulator and preparation method thereof |
CN108395225A (en) * | 2018-04-11 | 2018-08-14 | 佛山市拓拓网络科技有限公司 | A kind of electronic ceramics |
Non-Patent Citations (4)
Title |
---|
TAOYONG LIU ET.AL: "The utilization of electrical insulators waste and red mud for fabrication of partially vitrified ceramic materials with high porosity and high strength", 《JOURNAL OF CLEANER PRODUCTION》 * |
孔令同: "改性纳米硼酸铈的制备及其在润滑油中的应用", 《中国优秀硕士学位论文库》 * |
桑建华: "湿法成形轻质高强棒形支柱瓷绝缘子配方的研制", 《现代技术陶瓷》 * |
韦东田 等: "电瓷绝缘子中几种关键性粘土矿物原料研究", 《矿物学报》 * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110922157A (en) * | 2019-12-18 | 2020-03-27 | 江西省萍乡市南坑高压电瓷有限公司 | Electroceramic blank and manufacturing method thereof |
CN111099882A (en) * | 2019-12-30 | 2020-05-05 | 湖南高强电瓷电器有限公司 | High-strength ultrahigh-voltage hollow porcelain insulator and preparation method thereof |
CN112919882A (en) * | 2021-03-30 | 2021-06-08 | 江西省萍乡市华东出口电瓷有限公司 | High-strength high-hardness weather-resistant porcelain insulator and preparation method thereof |
CN112919882B (en) * | 2021-03-30 | 2022-09-16 | 江西省萍乡市华东出口电瓷有限公司 | High-strength high-hardness weather-resistant porcelain insulator and preparation method thereof |
CN113402932A (en) * | 2021-07-01 | 2021-09-17 | 江西东维电气有限公司 | Self-cleaning type high strength clavate porcelain insulator |
CN115974534A (en) * | 2023-02-07 | 2023-04-18 | 江西省萍乡市华东出口电瓷有限公司 | Suspension porcelain insulator with aluminum oxide cylindrical head structure |
CN115974534B (en) * | 2023-02-07 | 2023-09-08 | 江西省萍乡市华东出口电瓷有限公司 | Suspension porcelain insulator with alumina cylindrical head structure |
Also Published As
Publication number | Publication date |
---|---|
CN110467442B (en) | 2021-12-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110467442A (en) | A kind of high-strength porcelain insulator and preparation method thereof | |
CN105645823B (en) | A kind of low-dosage green alkali-free chlorine liquid accelerator and preparation method thereof | |
CN112919882B (en) | High-strength high-hardness weather-resistant porcelain insulator and preparation method thereof | |
CN105385870A (en) | Preparation method of graphene/aluminum composite material | |
CN106007657B (en) | A kind of preparation method of pillar porcelain insulator | |
CN110950633A (en) | Electric porcelain insulator and preparation method thereof | |
CN112707714A (en) | Formula and preparation process of high-strength cylindrical head suspension insulator | |
CN104446277A (en) | Electro-ceramic cement adhesive composite material prescription | |
CN106007656B (en) | A kind of pillar porcelain insulator | |
CN113354437A (en) | Toughening column type porcelain insulator and preparation method thereof | |
CN101767984B (en) | Fused silica ceramic material containing holmium oxide and preparation method thereof | |
CN108624087B (en) | Pretreatment method of zircon powder with high reaction activity | |
CN106882950B (en) | Method for enhancing high-temperature-resistant phosphate adhesive by using silica sol | |
CN115974534B (en) | Suspension porcelain insulator with alumina cylindrical head structure | |
CN106221082B (en) | A kind of composite material and preparation method of Gemini surface active modified calcium carbonate filled polytetrafluoroethylene | |
CN104497211A (en) | Efficient concrete thickener and preparation method thereof | |
CN110903071A (en) | Electric porcelain insulator and preparation method thereof | |
EP4310829A1 (en) | Iron-modified acoustic material, production method thereof, speaker and electronic device | |
CN110922157A (en) | Electroceramic blank and manufacturing method thereof | |
CN111484321A (en) | Ultrahigh-strength domestic ceramic and preparation method thereof | |
CN109627033A (en) | A kind of heat-insulated ceramic ware for daily use and preparation method thereof | |
CN111704783B (en) | Preparation process of finishing powder | |
CN111041267A (en) | High-purity gold-based silver-palladium composite bonding material | |
JPH0356581A (en) | Silicone two-component type sealing material composition | |
US4036907A (en) | Poly(meta-phenylene isophthalamide) composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |