CN105198388A - Preparation method of ceramic binding post used for high voltage suspension type electric power - Google Patents

Preparation method of ceramic binding post used for high voltage suspension type electric power Download PDF

Info

Publication number
CN105198388A
CN105198388A CN201510615822.5A CN201510615822A CN105198388A CN 105198388 A CN105198388 A CN 105198388A CN 201510615822 A CN201510615822 A CN 201510615822A CN 105198388 A CN105198388 A CN 105198388A
Authority
CN
China
Prior art keywords
parts
oxide
preparation
high voltage
electric power
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201510615822.5A
Other languages
Chinese (zh)
Other versions
CN105198388B (en
Inventor
刘贞天
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hunan Xingcheng Electric Porcelain Electrical Appliances Co., Ltd.
Original Assignee
Changsha Dingcheng New Material Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Changsha Dingcheng New Material Technology Co Ltd filed Critical Changsha Dingcheng New Material Technology Co Ltd
Priority to CN201810197324.7A priority Critical patent/CN108314429A/en
Priority to CN201510615822.5A priority patent/CN105198388B/en
Priority to CN201810197325.1A priority patent/CN108298962A/en
Publication of CN105198388A publication Critical patent/CN105198388A/en
Application granted granted Critical
Publication of CN105198388B publication Critical patent/CN105198388B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention discloses a preparation method of a ceramic binding post used in high voltage suspension type electric power. According to the preparation method, a solid phase sintering method is adopted, nanometer alumimum oxide, barium titanate and sericite serve as main raw materials, methyl vinyl silicone rubber, mullite, talc, clay, celestine, zirconium oxide provided with stable yttrium, zinc oxide and titanium oxide serve as auxiliary constituents, iron oxide, niobium oxide, manganese dioxide, anti-explosion fibers, chromium oxide and nickel oxide serve as additives, and the ceramic binding post which is high in compression strength and used in high voltage suspension type electric power is prepared and obtained.

Description

A kind of preparation method of high voltage suspended electric power ceramic wiring terminal
Technical field
The invention belongs to a kind of preparation method of high voltage suspended electric power ceramic wiring terminal, belong to ceramic field.
Background technology
Terminal stud is widely used in various vacuum device, plays High-Voltage Insulation, vacuum-sealing and supports the effects such as fixing.Ceramic wiring terminal is terminal stud the most common.At high voltage suspended power domain, also widely, the research about ceramic wiring terminal is also very general in the application of ceramic wiring terminal.But along with the further miniaturization of electrical device and integrated, the voltage endurance capability improving high voltage suspended electric power ceramic wiring terminal becomes the concern of this field and one of problem demanding prompt solution.
Summary of the invention
The object of the invention is for the problems referred to above, develop a kind of preparation method with the high voltage suspended electric power ceramic wiring terminal of alumina base of high compressive strength.
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 10-50 part;
Barium titanate 10-50 part;
Sericite 10-50 part;
Methyl vinyl silicone rubber 5-15 part;
Mullite 5-15 part;
Talcum 5-15 part;
Clay 5-15 part;
Lazurite 5-15 part;
Zirconium white 5-15 part that yttrium is stable;
Zinc oxide 5-15 part;
Titanium oxide 5-15 part;
Ferric oxide 1-4 part;
Niobium oxides 1-4 part;
Manganse Dioxide 1-4 part;
Explosion-proof fiber 1-4 part;
Chromic oxide 1-4 part;
Nickel oxide 1-4 part;
(2) pre-burning: mixed by each raw material, at 200-300 degree Celsius of lower pre-burning 1-3 hour, obtains Preburning material;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 24-48 hour;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 600-650 DEG C, burn till 1-2 hour, and then calcine 1-2 hour at 1500-1600 DEG C.
As preferably: described pre-burning, 250 degrees Celsius of lower pre-burnings 2 hours, obtains Preburning material.
As preferably: the weight part of each raw material is:
Nano aluminium oxide 30 parts;
Barium titanate 30 parts;
Sericite 30 parts;
Methyl vinyl silicone rubber 9 parts;
Mullite 9 parts;
9 parts, talcum;
Clay 9 parts;
Lazurite 7 parts;
The zirconium white 7 parts that yttrium is stable;
7 parts, zinc oxide;
Titanium oxide 7 parts;
Ferric oxide 2 parts;
Niobium oxides 2 parts;
Manganse Dioxide 2 parts;
Explosion-proof fiber 2 parts;
1 part, chromic oxide;
Nickel oxide 1 part.
As preferably: the particle diameter of described nano aluminium oxide is 30-70nm.
As preferably: the time of described ball milling step is 36 hours.
As preferably: described in burn till burn till 1.5 hours at 620 DEG C, and then to calcine 1.5 hours at 1550 DEG C.
Beneficial effect of the present invention:
By reasonable preparation raw material, adopt the method for solid state sintering, with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive, have prepared the high voltage suspended electric power ceramic wiring terminal with high compressive strength.
The present invention is in the selection of main raw material, the nano aluminium oxide adopting physical and chemical performance more superior is as main material, by selecting the aluminum oxide of Nano grade, it has larger specific surface area and more superior tap density and more excellent mechanical property and anti-pressure ability.Simultaneously, the three kinds of materials that employ of the invention are main material, barium titanate and sericite, not only from the main material cost reducing nano aluminium oxide, meanwhile, also by the supplement effect of laminate structure, create supplement effect, meanwhile, heat-resisting, the resistance to compression of sericite and barium titanate and whippy physics and chemistry function, will produce synergistic effect and devotion effect to nano aluminium oxide.Meanwhile, also containing a lot of trace element in sericite, certain sintering aid effect will be played in sintering process.And in the selection of auxiliary material, methyl vinyl silicone rubber is modified rubber, by the compound with inorganic materials, the mechanical property of stupalith can be improved; And the stable zirconium white of mullite, talcum, clay, lazurite, yttrium plays enhancement for the performance such as anti-pressure and abrasion-proof strengthening stupalith.And the introducing of zinc oxide and titanium oxide, the self-cleaning ability of terminal stud can be improved; In the selection of additive, the present invention introduces multiple additives metal oxide, by the doping of metallic element, the performances such as the surface resistivity of pottery can be made to be optimized, then improve the voltage endurance capability of pottery.This ceramsite preparation process is simple, is applicable to suitability for industrialized production.
Embodiment
Below in conjunction with specific embodiment, and comparable data describes in further detail the present invention.Should be understood that these embodiments just in order to demonstrate the invention, but not limit the scope of the invention by any way.
Embodiment 1:
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 30 parts;
Barium titanate 30 parts;
Sericite 30 parts;
Methyl vinyl silicone rubber 9 parts;
Mullite 9 parts;
9 parts, talcum;
Clay 9 parts;
Lazurite 7 parts;
The zirconium white 7 parts that yttrium is stable;
7 parts, zinc oxide;
Titanium oxide 7 parts;
Ferric oxide 2 parts;
Niobium oxides 2 parts;
Manganse Dioxide 2 parts;
Explosion-proof fiber 2 parts;
1 part, chromic oxide;
Nickel oxide 1 part;
(2) pre-burning: mixed by each raw material, 250 degrees Celsius of lower pre-burnings 2 hours, obtains Preburning material;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 36 hours;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 650 DEG C, burn till 1.5 hours, and then calcine 1.5 hours at 1550 DEG C.
Embodiment 2:
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 35 parts;
Barium titanate 35 parts;
Sericite 35 parts;
Methyl vinyl silicone rubber 11 parts;
Mullite 11 parts;
11 parts, talcum;
Clay 11 parts;
Lazurite 7 parts;
The zirconium white 7 parts that yttrium is stable;
7 parts, zinc oxide;
Titanium oxide 7 parts;
Ferric oxide 1 part;
Niobium oxides 2 parts;
Manganse Dioxide 1 part;
Explosion-proof fiber 2 parts;
2 parts, chromic oxide;
Nickel oxide 1 part;
(2) pre-burning: each raw material is mixed, pre-burning 3 hours, obtains Preburning material at 300 degrees Celsius;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 48 hours;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 650 DEG C, burn till 2 hours, and then calcine 2 hours at 1600 DEG C.
Embodiment 3:
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 50 parts;
Barium titanate 50 parts;
Sericite 50 parts;
Methyl vinyl silicone rubber 15 parts;
Mullite 15 parts;
15 parts, talcum;
Clay 15 parts;
Lazurite 7 parts;
The zirconium white 7 parts that yttrium is stable;
7 parts, zinc oxide;
Titanium oxide 7 parts;
Ferric oxide 2 parts;
Niobium oxides 2 parts;
Manganse Dioxide 2 parts;
Explosion-proof fiber 2 parts;
1 part, chromic oxide;
Nickel oxide 1 part;
(2) pre-burning: each raw material is mixed, pre-burning 1 hour, obtains Preburning material at 200 degrees celsius;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 24 hours;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 600 DEG C, burn till 1 hour, and then calcine 1 hour at 1500 DEG C.
Embodiment 4:
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 10 parts;
Barium titanate 10 parts;
Sericite 10 parts;
Methyl vinyl silicone rubber 5 parts;
Mullite 5 parts;
5 parts, talcum;
Clay 5 parts;
Lazurite 5 parts;
The zirconium white 5 parts that yttrium is stable;
5 parts, zinc oxide;
Titanium oxide 5 parts;
Ferric oxide 1 part;
Niobium oxides 1 part;
Manganse Dioxide 1 part;
Explosion-proof fiber 1 part;
1 part, chromic oxide;
Nickel oxide 1 part;
(2) pre-burning: each raw material is mixed, pre-burning 1 hour, obtains Preburning material at 200 degrees celsius;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 24 hours;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 600 DEG C, burn till 1 hour, and then calcine 1 hour at 1500 DEG C.
Embodiment 5:
A preparation method for high voltage suspended electric power ceramic wiring terminal,
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 50 parts;
Barium titanate 50 parts;
Sericite 35 parts;
Methyl vinyl silicone rubber 10 parts;
Mullite 10 parts;
10 parts, talcum;
Clay 10 parts;
Lazurite 10 parts;
The zirconium white 10 parts that yttrium is stable;
10 parts, zinc oxide;
Titanium oxide 10 parts;
Ferric oxide 3 parts;
Niobium oxides 3 parts;
Manganse Dioxide 3 parts;
Explosion-proof fiber 3 parts;
3 parts, chromic oxide;
Nickel oxide 3 parts;
(2) pre-burning: mixed by each raw material, 250 degrees Celsius of lower pre-burnings 2 hours, obtains Preburning material;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 36 hours;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 625 DEG C, burn till 1 hour, and then calcine 1 hour at 1550 DEG C.
The physical measurement data of the embodiment of the present invention are as follows:
Vickers' hardness/Gpa Ultimate compression strength/Mpa Specific inductivity
Embodiment 1 66 790 9.08
Embodiment 2 69 800 8.99
Embodiment 3 68 795 9.12
Embodiment 4 65 815 9.15
Embodiment 5 70 810 9.20
To those skilled in the art, obviously the invention is not restricted to the details of above-mentioned one exemplary embodiment, and when not deviating from spirit of the present invention or essential characteristic, the present invention can be realized in other specific forms.Therefore, no matter from which point, all should embodiment be regarded as exemplary, and be nonrestrictive, scope of the present invention is limited by claims instead of above-mentioned explanation, and all changes be therefore intended in the implication of the equivalency by dropping on claim and scope are included in the present invention.
In addition, be to be understood that, although this specification sheets is described according to embodiment, but not each embodiment only comprises an independently technical scheme, this narrating mode of specification sheets is only for clarity sake, those skilled in the art should by specification sheets integrally, and the technical scheme in each embodiment also through appropriately combined, can form other embodiments that it will be appreciated by those skilled in the art that.

Claims (7)

1. a preparation method for high voltage suspended electric power ceramic wiring terminal, is characterized in that:
The preparation method of described ceramic wiring terminal comprises following preparation process:
(1) get the raw materials ready: with nano aluminium oxide, barium titanate and sericite for main raw material, with stable zirconium white, zinc oxide and the titanium oxide of methyl vinyl silicone rubber, mullite, talcum, clay, lazurite, yttrium for ancillary component, with ferric oxide, niobium oxides, Manganse Dioxide, explosion-proof fiber, chromic oxide and nickel oxide are additive;
The weight part of each raw material is:
Nano aluminium oxide 10-50 part;
Barium titanate 10-50 part;
Sericite 10-50 part;
Methyl vinyl silicone rubber 5-15 part;
Mullite 5-15 part;
Talcum 5-15 part;
Clay 5-15 part;
Lazurite 5-15 part;
Zirconium white 5-15 part that yttrium is stable;
Zinc oxide 5-15 part;
Titanium oxide 5-15 part;
Ferric oxide 1-4 part;
Niobium oxides 1-4 part;
Manganse Dioxide 1-4 part;
Explosion-proof fiber 1-4 part;
Chromic oxide 1-4 part;
Nickel oxide 1-4 part;
(2) pre-burning: mixed by each raw material, at 200-300 degree Celsius of lower pre-burning 1-3 hour, obtains Preburning material;
(3) ball milling: Preburning material is mixed, then adds appropriate water, according to Preburning material: ball: water=1:2:1, ball milling 24-48 hour;
(4) granulating and forming: by the granulation of ball milling material, and cold isostatic compaction;
(5) burn till: at 600-650 DEG C, burn till 1-2 hour, and then calcine 1-2 hour at 1500-1600 DEG C.
2. a preparation method for high voltage suspended electric power ceramic wiring terminal as claimed in claim 2, is characterized in that: described pre-burning, 250 degrees Celsius of lower pre-burnings 2 hours, obtains Preburning material.
3. a preparation method for high voltage suspended electric power ceramic wiring terminal as claimed in claim 1 or 2, is characterized in that: the weight part of each raw material is:
Nano aluminium oxide 30 parts;
Barium titanate 30 parts;
Sericite 30 parts;
Methyl vinyl silicone rubber 9 parts;
Mullite 9 parts;
9 parts, talcum;
Clay 9 parts;
Lazurite 7 parts;
The zirconium white 7 parts that yttrium is stable;
7 parts, zinc oxide;
Titanium oxide 7 parts;
Ferric oxide 2 parts;
Niobium oxides 2 parts;
Manganse Dioxide 2 parts;
Explosion-proof fiber 2 parts;
1 part, chromic oxide;
Nickel oxide 1 part.
4. a preparation method for high voltage suspended electric power ceramic wiring terminal as claimed in claim 3, is characterized in that: the particle diameter of described nano aluminium oxide is 30-70nm.
5. a preparation method for high voltage suspended electric power ceramic wiring terminal as claimed in claim 1, is characterized in that: the time of described ball milling step is 36 hours.
6. a preparation method for high voltage suspended electric power ceramic wiring terminal as claimed in claim 1, is characterized in that: described in burn till burn till 1.5 hours at 620 DEG C, and then to calcine 1.5 hours at 1550 DEG C.
7. the high voltage suspended electric power ceramic wiring terminal for preparing of the preparation method of high voltage suspended electric power ceramic wiring terminal any one of a claim 1-6.
CN201510615822.5A 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended electric power ceramic wiring terminal Active CN105198388B (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN201810197324.7A CN108314429A (en) 2015-09-24 2015-09-24 A kind of preparation method of higfh-tension ceramics binding post
CN201510615822.5A CN105198388B (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended electric power ceramic wiring terminal
CN201810197325.1A CN108298962A (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended ceramic wiring terminal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510615822.5A CN105198388B (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended electric power ceramic wiring terminal

Related Child Applications (2)

Application Number Title Priority Date Filing Date
CN201810197325.1A Division CN108298962A (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended ceramic wiring terminal
CN201810197324.7A Division CN108314429A (en) 2015-09-24 2015-09-24 A kind of preparation method of higfh-tension ceramics binding post

Publications (2)

Publication Number Publication Date
CN105198388A true CN105198388A (en) 2015-12-30
CN105198388B CN105198388B (en) 2018-04-24

Family

ID=54946416

Family Applications (3)

Application Number Title Priority Date Filing Date
CN201810197324.7A Pending CN108314429A (en) 2015-09-24 2015-09-24 A kind of preparation method of higfh-tension ceramics binding post
CN201810197325.1A Withdrawn CN108298962A (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended ceramic wiring terminal
CN201510615822.5A Active CN105198388B (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended electric power ceramic wiring terminal

Family Applications Before (2)

Application Number Title Priority Date Filing Date
CN201810197324.7A Pending CN108314429A (en) 2015-09-24 2015-09-24 A kind of preparation method of higfh-tension ceramics binding post
CN201810197325.1A Withdrawn CN108298962A (en) 2015-09-24 2015-09-24 A kind of preparation method of high voltage suspended ceramic wiring terminal

Country Status (1)

Country Link
CN (3) CN108314429A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107129289A (en) * 2017-06-01 2017-09-05 合肥尚强电气科技有限公司 A kind of insulator and preparation method thereof
CN108101526A (en) * 2017-12-13 2018-06-01 萍乡强盛电瓷制造有限公司 A kind of electric porcelain insulator and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101404360A (en) * 2008-10-21 2009-04-08 潮州市三江电子有限公司 Connector post of refrigeration compressor
CN101624290A (en) * 2009-07-24 2010-01-13 中国科学院上海硅酸盐研究所 Preparation method of high-transparent fine-grained alumina ceramics
CN101993239A (en) * 2010-11-29 2011-03-30 中国科学院上海硅酸盐研究所 Method for preparing fine-grain high-strength high-purity alumina ceramics
CN102153335A (en) * 2011-04-02 2011-08-17 西南科技大学 Machinable aluminium oxide ceramics and preparation method of machinable aluminium oxide ceramics

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101941836B (en) * 2010-08-30 2013-01-02 济源市更新瓷料有限公司 Low-temperature ceramic-firing high-density alumina ceramic granulation powder and preparation method thereof
CN103739273B (en) * 2013-12-23 2015-05-20 吴江华诚复合材料科技有限公司 Insulating ceramic material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101404360A (en) * 2008-10-21 2009-04-08 潮州市三江电子有限公司 Connector post of refrigeration compressor
CN101624290A (en) * 2009-07-24 2010-01-13 中国科学院上海硅酸盐研究所 Preparation method of high-transparent fine-grained alumina ceramics
CN101993239A (en) * 2010-11-29 2011-03-30 中国科学院上海硅酸盐研究所 Method for preparing fine-grain high-strength high-purity alumina ceramics
CN102153335A (en) * 2011-04-02 2011-08-17 西南科技大学 Machinable aluminium oxide ceramics and preparation method of machinable aluminium oxide ceramics

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107129289A (en) * 2017-06-01 2017-09-05 合肥尚强电气科技有限公司 A kind of insulator and preparation method thereof
CN108101526A (en) * 2017-12-13 2018-06-01 萍乡强盛电瓷制造有限公司 A kind of electric porcelain insulator and preparation method thereof
CN108101526B (en) * 2017-12-13 2020-07-17 萍乡强盛电瓷制造有限公司 Electric porcelain insulator and preparation method thereof

Also Published As

Publication number Publication date
CN108298962A (en) 2018-07-20
CN105198388B (en) 2018-04-24
CN108314429A (en) 2018-07-24

Similar Documents

Publication Publication Date Title
Zhao et al. High-energy storage performance in lead-free (1-x) BaTiO3-xBi (Zn0. 5Ti0. 5) O3 relaxor ceramics for temperature stability applications
CN105254288A (en) Preparation method of electric organic composite ceramic binding post
KR101228689B1 (en) Oxide based magnetic material, process for producing the same, sintered ferrite magnet and process for producing the same
Jian et al. A strategy for design of non-percolative composites with stable giant dielectric constants and high energy densities
BRPI0620713A2 (en) magnetic oxide material
CN105692641A (en) Preparation method and application of tungsten boride
CN105949725A (en) Epoxy-resin-based high-dielectric composite material and preparation method thereof
CN105198407A (en) Preparation method of composite ceramic binding post for electricity
CN105198388A (en) Preparation method of ceramic binding post used for high voltage suspension type electric power
CN108409320B (en) Double-texture composite magneto-dielectric ceramic material and preparation method thereof
Jotania et al. Structural phases and Maxwell–Wagner relaxation in magnetically soft-ZnFe2O4 and hard-Sr2Cu2Fe12O22 nanocomposites
CN100532319C (en) Mo-corundum ceramic material and low-temperature sintering method
CN105130406A (en) Preparation method of high-voltage suspension type alumina-based ceramic binding post for electric power
CN103113125A (en) Lamellar compound platy crystal grain dispersed and enhanced transition metal carbide multiphase material and ultralow temperature preparation method thereof
CN105254289A (en) Preparation method of electricity inorganic composite ceramic binding post
CN104710171B (en) A kind of high energy storage density strontium bismuth titanate base complex phase ceramic and preparation method thereof
Zahi et al. Preparation of Ni–Zn–Cu ferrite particles by sol–gel technique
Zhang et al. Preparation and dielectric properties of (Ba0. 5Sr0. 4Ca0. 1) TiO3/polystyrene composites
JP2007055832A (en) Oxide magnetic composition and magnetic material for high frequency
JP4461276B2 (en) Method for producing magnetic powder
JP4761187B2 (en) Magnetic oxide material
CN104710172B (en) A kind of lead-free anti-ferroelectric high energy storage density ceramic material and preparation method thereof
CN107586060A (en) A kind of High-energy-storage density dielectric material and preparation method thereof
JP6195110B2 (en) Oxide ceramics and ceramic electronic parts
CN103288441B (en) The Meta Materials of a kind of ceramic composite and preparation thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20180320

Address after: 362000 Dongping City, Quanzhou province Yongchun town Dongshan village, No. 579, No.

Applicant after: Yan Rongtu

Address before: 410205 A543, Changsha, China, the headquarters of the software park, No. 39, sharp mountain road, high tech Development Zone, Hunan, China

Applicant before: CHANGSHA DINGCHENG NEW MATERIAL TECHNOLOGY CO., LTD.

GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20191122

Address after: 412200 No. three, 6 Liling Road, Hunan, Zhuzhou

Patentee after: Hunan Xingcheng Electric Porcelain Electrical Appliances Co., Ltd.

Address before: 362000 Dongping City, Quanzhou province Yongchun town Dongshan village, No. 579, No.

Patentee before: Yan Rongtu