CN106242581A - A kind of high performance ceramic material and the application in preparing sintex thereof - Google Patents
A kind of high performance ceramic material and the application in preparing sintex thereof Download PDFInfo
- Publication number
- CN106242581A CN106242581A CN201610580411.1A CN201610580411A CN106242581A CN 106242581 A CN106242581 A CN 106242581A CN 201610580411 A CN201610580411 A CN 201610580411A CN 106242581 A CN106242581 A CN 106242581A
- Authority
- CN
- China
- Prior art keywords
- parts
- borax
- sodium metasilicate
- ceramic material
- granule
- 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
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/58—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
- C04B35/584—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon nitride
-
- 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
- C04B35/64—Burning or sintering processes
- C04B35/645—Pressure sintering
-
- 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
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
-
- 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
- C04B2235/3241—Chromium oxides, chromates, 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
- C04B2235/3298—Bismuth oxides, bismuthates or oxide forming salts thereof, e.g. zinc bismuthate
-
- 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
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3826—Silicon carbides
Abstract
The invention discloses a kind of high performance ceramic material and the application in preparing sintex thereof, be prepared from by the raw material of following weight portion: silicon nitride, 80~90 parts;Chromium oxide, 3~5 parts;Carborundum, 4~6 parts;Silicon dioxide, 3~5 parts;Titanium dioxide, 4~6 parts;Calcium fluoride, 2~4 parts;Calcium pyroborate, 1~3 part;Bismuth oxide, 2~4 parts;Polyethylene Glycol, 0.8~1.2 part;Polyacrylic acid, 0.6~0.8 part;Deionized water, 25~35 parts;Borax and sodium metasilicate totally 6~8 parts, the weight ratio of Borax and sodium metasilicate is 5~7:1.The ceramic material toughness that the present invention provides is high, hardness is high, and intensity is big, is suitable for use as ceramic cutting tool material.This technique effect is relevant with the weight ratio of Borax in raw material and sodium metasilicate, when the weight ratio of Borax and sodium metasilicate is 5~7:1, and the best performance of ceramic material.
Description
Technical field
The present invention relates to cutter material field, be specifically related to a kind of high performance ceramic material and in preparing sintex
Application.
Background technology
Ceramic cutting-tool has possessed high rigidity, high density, high temperature resistant, and diamagneticization, antioxidation, corrosion resistance are strong, chemical
The feature such as good stability, high-wearing feature, is the succedaneum that the tradition cutting elements such as high-speed steel are good, solves the resource such as molybdenum, nickel
Rare problem.But ceramic cutting material still exists relatively costly at present, toughness is inadequate, fragility is big, hardness is uneven,
The problems such as poor radiation, self lubricity are bad, need to solve.
Summary of the invention
It is an object of the invention to provide a kind of high performance ceramic material and the application in preparing sintex thereof.
The above-mentioned purpose of the present invention is achieved by techniques below scheme:
A kind of high performance ceramic material, is prepared from by the raw material of following weight portion: silicon nitride, 80~90 parts;Oxidation
Chromium, 3~5 parts;Carborundum, 4~6 parts;Silicon dioxide, 3~5 parts;Titanium dioxide, 4~6 parts;Calcium fluoride, 2~4 parts;Calcium pyroborate,
1~3 part;Bismuth oxide, 2~4 parts;Polyethylene Glycol, 0.8~1.2 part;Polyacrylic acid, 0.6~0.8 part;Deionized water, 25~35
Part;Borax and sodium metasilicate totally 6~8 parts, the weight ratio of Borax and sodium metasilicate is 5~7:1.
Further, described high performance ceramic material is prepared from by the raw material of following weight portion: silicon nitride, and 85
Part;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3 parts;Calcium pyroborate, 2 parts;Oxidation
Bismuth, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax and sodium metasilicate totally 7 parts, Borax and
The weight ratio of sodium metasilicate is 6:1.
Further, described high performance ceramic material is prepared from by the raw material of following weight portion: silicon nitride, and 80
Part;Chromium oxide, 3 parts;Carborundum, 4 parts;Silicon dioxide, 3 parts;Titanium dioxide, 4 parts;Calcium fluoride, 2 parts;Calcium pyroborate, 1 part;Oxidation
Bismuth, 2 parts;Polyethylene Glycol, 0.8 part;Polyacrylic acid, 0.6 part;Deionized water, 25 parts;Borax and sodium metasilicate totally 6 parts, Borax and
The weight ratio of sodium metasilicate is 5:1.
Further, described high performance ceramic material is prepared from by the raw material of following weight portion: silicon nitride, and 90
Part;Chromium oxide, 5 parts;Carborundum, 6 parts;Silicon dioxide, 5 parts;Titanium dioxide, 6 parts;Calcium fluoride, 4 parts;Calcium pyroborate, 3 parts;Oxidation
Bismuth, 4 parts;Polyethylene Glycol, 1.2 parts;Polyacrylic acid, 0.8 part;Deionized water, 35 parts;Borax and sodium metasilicate totally 8 parts, Borax and
The weight ratio of sodium metasilicate is 7:1.
The preparation method of above-mentioned high performance ceramic material, comprises the steps:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, granule step S1, S2 obtained mixes, and adds deionized water and is mixed into pureed, sends in ball mill
Ball milling 2~3 hours, be dried, and sends in calcining furnace, calcines 1~2 hour at 800~900 DEG C, take out and pulverize, crosses 200 mesh
Sieve, obtains granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2~3 is little
Time, to dry at 110~120 DEG C, cross 40 mesh sieves, hot pressing at 1600~1700 DEG C, hot pressing pressure is 20~30MPa, hot pressing
Time is 50~60 minutes, to obtain final product.
Advantages of the present invention:
The ceramic material toughness that the present invention provides is high, hardness is high, and intensity is big, is suitable for use as ceramic cutting tool material.
Detailed description of the invention
Further illustrate the essentiality content of the present invention below in conjunction with embodiment, but do not limit the present invention with this and protect model
Enclose.Although the present invention being explained in detail with reference to preferred embodiment, it will be understood by those within the art that, can be right
Technical scheme is modified or equivalent, without deviating from the spirit and scope of technical solution of the present invention.
Embodiment 1: the preparation of high performance ceramic material
Parts by weight of raw materials compares:
Silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3
Part;Calcium pyroborate, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax is with inclined
Sodium silicate totally 7 parts, the weight ratio of Borax and sodium metasilicate is 6:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
Embodiment 2: the preparation of high performance ceramic material
Parts by weight of raw materials compares:
Silicon nitride, 80 parts;Chromium oxide, 3 parts;Carborundum, 4 parts;Silicon dioxide, 3 parts;Titanium dioxide, 4 parts;Calcium fluoride, 2
Part;Calcium pyroborate, 1 part;Bismuth oxide, 2 parts;Polyethylene Glycol, 0.8 part;Polyacrylic acid, 0.6 part;Deionized water, 25 parts;Borax is with inclined
Sodium silicate totally 6 parts, the weight ratio of Borax and sodium metasilicate is 5:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
Embodiment 3: the preparation of high performance ceramic material
Parts by weight of raw materials compares:
Silicon nitride, 90 parts;Chromium oxide, 5 parts;Carborundum, 6 parts;Silicon dioxide, 5 parts;Titanium dioxide, 6 parts;Calcium fluoride, 4
Part;Calcium pyroborate, 3 parts;Bismuth oxide, 4 parts;Polyethylene Glycol, 1.2 parts;Polyacrylic acid, 0.8 part;Deionized water, 35 parts;Borax is with inclined
Sodium silicate totally 8 parts, the weight ratio of Borax and sodium metasilicate is 7:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
Embodiment 4: the preparation of high performance ceramic material
Parts by weight of raw materials compares:
Silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3
Part;Calcium pyroborate, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax is with inclined
Sodium silicate totally 7 parts, the weight ratio of Borax and sodium metasilicate is 5:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
Embodiment 5: the preparation of high performance ceramic material
Parts by weight of raw materials compares:
Silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3
Part;Calcium pyroborate, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax is with inclined
Sodium silicate totally 7 parts, the weight ratio of Borax and sodium metasilicate is 7:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
The weight ratio of embodiment 6: comparative example, Borax and sodium metasilicate is 4:1
Parts by weight of raw materials compares:
Silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3
Part;Calcium pyroborate, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax is with inclined
Sodium silicate totally 7 parts, the weight ratio of Borax and sodium metasilicate is 4:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
The weight ratio of embodiment 7: comparative example, Borax and sodium metasilicate is 8:1
Parts by weight of raw materials compares:
Silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3
Part;Calcium pyroborate, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax is with inclined
Sodium silicate totally 7 parts, the weight ratio of Borax and sodium metasilicate is 8:1.
Preparation method:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate
Close, ball milling, cross 200 mesh sieves, obtain granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, by step S1, the mixing of S2 granule, adds deionized water and is mixed into pureed, send into ball milling 2.5 in ball mill
Individual hour, it is dried, sends in calcining furnace, calcine 1.5 hours at 850 DEG C, take out and pulverize, cross 200 mesh sieves, obtain granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, and ball milling 2.5 is little
Time, to dry at 115 DEG C, cross 40 mesh sieves, hot pressing at 1650 DEG C, hot pressing pressure is 25MPa, and hot pressing time is 55 minutes.
Embodiment 8: effect example
The performance of the ceramic material of testing example 1~7 preparation respectively, result is as follows.
Fracture toughness/MPa m1/2 | Vickers hardness/GPa | Bending strength/MPa | |
Embodiment 1 | 17.5 | 95 | 1280 |
Embodiment 4 | 17.1 | 92 | 1240 |
Embodiment 5 | 17.3 | 92 | 1250 |
Embodiment 6 | 9.6 | 65 | 750 |
Embodiment 7 | 9.4 | 63 | 780 |
The test result of embodiment 2,3 is basically identical with embodiment 4,5.
Above-mentioned test result indicate that, the ceramic material toughness that the present invention provides is high, hardness is high, and intensity is big, is suitable for use as pottery
Porcelain cutter material.This technique effect is relevant with the weight ratio of Borax in raw material and sodium metasilicate, Borax and sodium metasilicate
Weight ratio when being 5~7:1, the best performance of ceramic material.
The effect of above-described embodiment indicates that the essentiality content of the present invention, but does not limit the protection of the present invention with this
Scope.It will be understood by those within the art that, technical scheme can be modified or equivalent,
Essence and protection domain without deviating from technical solution of the present invention.
Claims (5)
1. a high performance ceramic material, it is characterised in that be prepared from by the raw material of following weight portion: silicon nitride, 80~
90 parts;Chromium oxide, 3~5 parts;Carborundum, 4~6 parts;Silicon dioxide, 3~5 parts;Titanium dioxide, 4~6 parts;Calcium fluoride, 2~4
Part;Calcium pyroborate, 1~3 part;Bismuth oxide, 2~4 parts;Polyethylene Glycol, 0.8~1.2 part;Polyacrylic acid, 0.6~0.8 part;Deionization
Water, 25~35 parts;Borax and sodium metasilicate totally 6~8 parts, the weight ratio of Borax and sodium metasilicate is 5~7:1.
High performance ceramic material the most according to claim 1, it is characterised in that by the raw material preparation of following weight portion
Become: silicon nitride, 85 parts;Chromium oxide, 4 parts;Carborundum, 5 parts;Silicon dioxide, 4 parts;Titanium dioxide, 5 parts;Calcium fluoride, 3 parts;Boron
Acid calcium, 2 parts;Bismuth oxide, 3 parts;Polyethylene Glycol, 1.0 parts;Polyacrylic acid, 0.7 part;Deionized water, 30 parts;Borax and metasilicic acid
Totally 7 parts of sodium, the weight ratio of Borax and sodium metasilicate is 6:1.
High performance ceramic material the most according to claim 1, it is characterised in that by the raw material preparation of following weight portion
Become: silicon nitride, 80 parts;Chromium oxide, 3 parts;Carborundum, 4 parts;Silicon dioxide, 3 parts;Titanium dioxide, 4 parts;Calcium fluoride, 2 parts;Boron
Acid calcium, 1 part;Bismuth oxide, 2 parts;Polyethylene Glycol, 0.8 part;Polyacrylic acid, 0.6 part;Deionized water, 25 parts;Borax and metasilicic acid
Totally 6 parts of sodium, the weight ratio of Borax and sodium metasilicate is 5:1.
High performance ceramic material the most according to claim 1, it is characterised in that by the raw material preparation of following weight portion
Become: silicon nitride, 90 parts;Chromium oxide, 5 parts;Carborundum, 6 parts;Silicon dioxide, 5 parts;Titanium dioxide, 6 parts;Calcium fluoride, 4 parts;Boron
Acid calcium, 3 parts;Bismuth oxide, 4 parts;Polyethylene Glycol, 1.2 parts;Polyacrylic acid, 0.8 part;Deionized water, 35 parts;Borax and metasilicic acid
Totally 8 parts of sodium, the weight ratio of Borax and sodium metasilicate is 7:1.
5. the preparation method of the arbitrary described high performance ceramic material of Claims 1 to 4, it is characterised in that comprise the steps:
Step S1, mixes chromium oxide, carborundum, silicon dioxide, calcium fluoride, Calcium pyroborate, bismuth oxide, Borax and sodium metasilicate,
Ball milling, crosses 200 mesh sieves, obtains granule;
Step S2, by silicon nitride, titanium dioxide mixing, ball milling, crosses 250 mesh sieves, obtains granule;
Step S3, granule step S1, S2 obtained mixes, and adds deionized water and is mixed into pureed, sends into ball milling 2 in ball mill
~3 hours, it is dried, sends in calcining furnace, calcine 1~2 hour at 800~900 DEG C, take out and pulverize, cross 200 mesh sieves,
To granule;
Step S4, granule step S3 obtained mixes with polyacrylic acid, Polyethylene Glycol, stirs, ball milling 2~3 hours,
Drying at 110~120 DEG C, cross 40 mesh sieves, hot pressing at 1600~1700 DEG C, hot pressing pressure is 20~30MPa, and hot pressing time is
50~60 minutes, to obtain final product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610580411.1A CN106242581B (en) | 2016-07-21 | 2016-07-21 | A kind of high performance ceramic material and its preparing the application in sintex |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610580411.1A CN106242581B (en) | 2016-07-21 | 2016-07-21 | A kind of high performance ceramic material and its preparing the application in sintex |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106242581A true CN106242581A (en) | 2016-12-21 |
CN106242581B CN106242581B (en) | 2019-02-19 |
Family
ID=57603214
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610580411.1A Active CN106242581B (en) | 2016-07-21 | 2016-07-21 | A kind of high performance ceramic material and its preparing the application in sintex |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106242581B (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104370555A (en) * | 2014-10-27 | 2015-02-25 | 合肥市东庐机械制造有限公司 | Silicon nitride based ceramic cutting tool material and preparation method thereof |
CN104370548A (en) * | 2014-10-27 | 2015-02-25 | 合肥市东庐机械制造有限公司 | Ceramic material for high-speed steel cutters and preparation method thereof |
CN104402420A (en) * | 2014-10-27 | 2015-03-11 | 合肥市东庐机械制造有限公司 | High toughness ceramic material for cutting tools and preparation method thereof |
CN105884388A (en) * | 2014-12-22 | 2016-08-24 | 青岛麦特瑞欧新材料技术有限公司 | Modified silicon carbide crystal whisker reinforced ceramic material and preparing method thereof |
-
2016
- 2016-07-21 CN CN201610580411.1A patent/CN106242581B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104370555A (en) * | 2014-10-27 | 2015-02-25 | 合肥市东庐机械制造有限公司 | Silicon nitride based ceramic cutting tool material and preparation method thereof |
CN104370548A (en) * | 2014-10-27 | 2015-02-25 | 合肥市东庐机械制造有限公司 | Ceramic material for high-speed steel cutters and preparation method thereof |
CN104402420A (en) * | 2014-10-27 | 2015-03-11 | 合肥市东庐机械制造有限公司 | High toughness ceramic material for cutting tools and preparation method thereof |
CN105884388A (en) * | 2014-12-22 | 2016-08-24 | 青岛麦特瑞欧新材料技术有限公司 | Modified silicon carbide crystal whisker reinforced ceramic material and preparing method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN106242581B (en) | 2019-02-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104229844B (en) | Preparation method of superfine low-sodium alpha-alumina powder with high activity | |
US10737983B2 (en) | Black zirconia sintered body and preparation method therefor and use thereof | |
CN104370550B (en) | A kind of high tenacity Stupalox material and preparation method thereof | |
CN103924144B (en) | A kind of soap-free emulsion polymeization phase ultrafine WC hard alloy preparation method | |
CN104387032B (en) | A kind of cutting tool pottery and its preparation method | |
CN107522465B (en) | A kind of preparation method of high-quality ceramics seal | |
WO2019210729A1 (en) | Caulking gypsum powder and preparation method therefor, and harmless treatment method for phosphogypsum | |
CN104370533B (en) | A kind of low cost ceramic cutter material and preparation method thereof | |
CN109369193A (en) | A kind of hard, silicon nitride ceramics of high-ductility performance and its preparation method and application with height | |
CN107176838A (en) | A kind of preparation method of the silicon carbide ceramics pot of graphene enhancing thermal conductivity | |
CN108165855B (en) | A kind of bonding agent, polycrystalline cubic boron nitride compound sheets and preparation method thereof | |
CN104370548B (en) | A kind of rapid steel cutting tool stupalith and preparation method thereof | |
CN104072143A (en) | High-thermal-conductivity silicon carbide ceramic material and preparation method thereof | |
CN106242581A (en) | A kind of high performance ceramic material and the application in preparing sintex thereof | |
CN106278254A (en) | A kind of high-strength and high ductility ceramic composite and the application in manufacturing cutter thereof | |
CN110204208A (en) | A kind of easy clean opal glaze and its preparation method and application suitable for low expansion ceramic | |
CN104402454A (en) | Heat-resistant ceramic for cutting tools and preparation method thereof | |
CN105060895A (en) | High-strength silicon carbide ceramic material and preparation method therefor | |
CN107043245B (en) | Ceramic heating sheet | |
CN104355615B (en) | A kind of high-hardness ceramic cutter material and preparation method thereof | |
CN109694242A (en) | It is a kind of suitable for electric cooker, the material of electric pressure cooking saucepan ceramic liner and its production technology | |
CN107858745A (en) | A kind of stainless steel products glossing | |
CN107056264A (en) | A kind of acid and alkali-resistance low-temperature sintering composite ceramic material and preparation method thereof | |
CN104387075B (en) | A kind of nozzle pottery containing diadust and preparation method thereof | |
KR101223455B1 (en) | Composition for heat resistance ceramic ware |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right |
Effective date of registration: 20200324 Address after: 311265, Hangzhou, Zhejiang province Xiaoshan district on the town of purple Village Patentee after: Zhejiang Ruike Special Ceramics Co., Ltd Address before: 325600 Zhejiang city of Wenzhou province Yueqing City Yuecheng Town Lake Ao Zhongyang road 37 Lane 2 Patentee before: Wang Hui |
|
TR01 | Transfer of patent right |