CN107935594A - The preparation method of low-k ultra high quality factor microwave-medium ceramics - Google Patents
The preparation method of low-k ultra high quality factor microwave-medium ceramics Download PDFInfo
- Publication number
- CN107935594A CN107935594A CN201810014956.5A CN201810014956A CN107935594A CN 107935594 A CN107935594 A CN 107935594A CN 201810014956 A CN201810014956 A CN 201810014956A CN 107935594 A CN107935594 A CN 107935594A
- Authority
- CN
- China
- Prior art keywords
- microwave
- preparation
- quality factor
- high quality
- ultra high
- 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.)
- Pending
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
- C04B35/495—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 vanadium, niobium, tantalum, molybdenum or tungsten oxides or solid solutions thereof with other oxides, e.g. vanadates, niobates, tantalates, molybdates or tungstates
-
- 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
- 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
- C04B2235/3213—Strontium 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
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3215—Barium 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
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
-
- 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
- C04B2235/3284—Zinc oxides, zincates, cadmium oxides, cadmiates, mercury oxides, mercurates 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
- C04B2235/34—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
- C04B2235/70—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)
- Inorganic Insulating Materials (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
This application discloses a kind of preparation method of low-k ultra high quality factor microwave-medium ceramics, stocked up by following molar ratio:0.15~0.25 barium carbonate;0.05~0.15 alundum (Al2O3);0.48~0.60 tantalum pentoxide;0.15~0.22 zinc oxide;0.01~0.03 strontium carbonate;0.03~0.05 silica prepares microwave-medium ceramics.The microwave-medium ceramics dielectric constant 20.0 ± 1.0 that the present invention obtains, and quality factor >=250000GHz.
Description
Technical field
This application involves the preparation method of microwave-medium ceramics, particularly a kind of low-k ultra high quality factor microwave
The preparation method of media ceramic.
Background technology
The microwave-medium ceramics of existing making can not meet low-k and two conditions of ultrahigh Q-value at the same time, can not
Meets the needs of existing production.
The content of the invention
The present invention is to overcome the deficiencies of the prior art and provide a kind of low-k ultra high quality factor microwave-medium
The preparation method of ceramics.
To achieve the above object, the present invention provides following technical solution:
The embodiment of the present application discloses the preparation method of low-k ultra high quality factor microwave-medium ceramics, including such as
Lower step,
S1 stocks up according to following molar ratio:0.15~0.25 barium carbonate;0.05~0.15 alundum (Al2O3);0.48~0.60
Tantalum pentoxide;0.15~0.22 zinc oxide;0.01~0.03 strontium carbonate;0.03~0.05 silica;
The barium carbonate, alundum (Al2O3), tantalum pentoxide, zinc oxide are mixed to form the first microwave material by S2, in institute
State and deionized water and zirconia balls progress ball milling are added in the first microwave material, dried after ball milling, then by steel wire
Mesh screen obtains the first powder;
S3 is by first powder calcination;
The strontium carbonate, silica the second microwave material of formation are added in the first powders of S4 after firing, described
Deionized water is added in second microwave material and carries out ball milling with zirconia balls, is dried after ball milling, then by steel wire
Sieve obtains the second powder;
S5 is by second powder calcination;
The second powder after calcining is put into polyesteramine bucket by S6, adds deionized water and zirconia balls, adds polyethylene
Alcohol solution after adding dispersant and releasing agent ball milling 24h, is granulated as binding agent;
S7 is pressed into granulation powder the sequin of radius 13.85mm, thickness 6.2mm;
The sequin suppressed is sintered 20h at a temperature of 1600~1650 DEG C and obtains product by S8.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S1, the barium carbonate, alundum (Al2O3), tantalum pentoxide, strontium carbonate, the purity of silica are more than 99.99%.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S2, first microwave material, deionized water, the mass ratio of zirconia balls are 1: 1.2: 2.5.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S2, drying temperature is 150 ± 5 DEG C, and the steel wire mesh screen is 200 mesh.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S3, calcining heat is 1350~1400 DEG C, calcination time 5h.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S4, second microwave material, deionized water, the mass ratio of zirconia balls are 1: 1.2: 2.5.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S4, drying temperature is 150 ± 5 DEG C, and the steel wire mesh screen is 200 mesh.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S5, calcining heat is 1400~1450 DEG C, calcination time 5h.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S6, the mass ratio of the second powder, deionized water, zirconia balls after calcining is 1: 1.0: 2.5.
Preferably, in the preparation method of above-mentioned low-k ultra high quality factor microwave-medium ceramics, the step
In rapid S9, the compact density of the sequin is 3.90 ± 0.10g/cm3。
The beneficial effects of the invention are as follows obtained microwave-medium ceramics dielectric constant 20.0 ± 1.0, and quality factor >=
250000GHz。
Embodiment
It will be apparent from the preferred embodiment of the present invention below.
Early-stage preparations raw material:Barium carbonate, alundum (Al2O3), tantalum pentoxide, strontium carbonate, the purity of silica are
More than 99.99%, nanoscale, purity zinc oxide reaches high-grade pure.
Embodiment 1
S1 stocks up according to following molar ratio:0.15 barium carbonate;0.15 alundum (Al2O3);0.52 tantalum pentoxide;0.15 oxygen
Change zinc;0.01 strontium carbonate;0.05 silica;
Barium carbonate, alundum (Al2O3), tantalum pentoxide, zinc oxide are mixed to form the first microwave material by S2, micro- first
Deionized water is added in wave material and carries out ball milling, the first microwave material, deionized water, the matter of zirconia balls with zirconia balls
Amount dries at 152 DEG C after ball milling than being 1: 1.2: 2.5, then obtains the first powder by 200 mesh steel wire mesh screens;
S3 is by the first powder calcination, and calcining heat is 1380 DEG C, calcination time 5h;
Strontium carbonate, silica the second microwave material of formation are added in the first powders of S4 after firing, in the second microwave
Deionized water is added in material and carries out ball milling, the second microwave material, deionized water, the quality of zirconia balls with zirconia balls
Than for 1: 1.2: 2.5, being dried after ball milling at 151 DEG C, then obtaining the second powder by 200 mesh steel wire mesh screens;
S5 is by the second powder calcination, and calcining heat is 1430 DEG C, calcination time 5h;
The second powder after calcining is put into polyesteramine bucket by S6, adds deionized water and zirconia balls, and the after calcining
Two powders, deionized water, the mass ratio of zirconia balls are 1: 1.0: 2.5, add polyvinyl alcohol water solution as binding agent, add
After entering dispersant and releasing agent ball milling 24h, it is granulated;
S7 is pressed into granulation powder the sequin of radius 13.85mm, thickness 6.2mm, and the compact density of sequin is
3.95g/cm3;
The sequin suppressed is sintered 20h at a temperature of 1630 DEG C and obtains product by S8.
Embodiment 2
S1 stocks up according to following molar ratio:0.22 barium carbonate;0.08 alundum (Al2O3);0.48 tantalum pentoxide;0.17 oxygen
Change zinc;0.02 strontium carbonate;0.04 silica;
Barium carbonate, alundum (Al2O3), tantalum pentoxide, zinc oxide are mixed to form the first microwave material by S2, micro- first
Deionized water is added in wave material and carries out ball milling, the first microwave material, deionized water, the matter of zirconia balls with zirconia balls
Amount dries at 153 DEG C after ball milling than being 1: 1.2: 2.5, then obtains the first powder by 200 mesh steel wire mesh screens;
S3 is by the first powder calcination, and calcining heat is 1375 DEG C, calcination time 5h;
Strontium carbonate, silica the second microwave material of formation are added in the first powders of S4 after firing, in the second microwave
Deionized water is added in material and carries out ball milling, the second microwave material, deionized water, the quality of zirconia balls with zirconia balls
Than for 1: 1.2: 2.5, being dried after ball milling at 150 DEG C, then obtaining the second powder by 200 mesh steel wire mesh screens;
S5 is by the second powder calcination, and calcining heat is 1440 DEG C, calcination time 5h;
The second powder after calcining is put into polyesteramine bucket by S6, adds deionized water and zirconia balls, and the after calcining
Two powders, deionized water, the mass ratio of zirconia balls are 1: 1.0: 2.5, add polyvinyl alcohol water solution as binding agent, add
After entering dispersant and releasing agent ball milling 24h, it is granulated;
S7 is pressed into granulation powder the sequin of radius 13.85mm, thickness 6.2mm, and the compact density of sequin is
3.92g/cm3;
The sequin suppressed is sintered 20h at a temperature of 1620 DEG C and obtains product by S8.
Embodiment 3
S1 stocks up according to following molar ratio:0.25 barium carbonate;0.05 alundum (Al2O3);0.60 tantalum pentoxide;0.22 oxygen
Change zinc;0.03 strontium carbonate;0.03 silica;
Barium carbonate, alundum (Al2O3), tantalum pentoxide, zinc oxide are mixed to form the first microwave material by S2, micro- first
Deionized water is added in wave material and carries out ball milling, the first microwave material, deionized water, the matter of zirconia balls with zirconia balls
Amount dries at 148 DEG C after ball milling than being 1: 1.2: 2.5, then obtains the first powder by 200 mesh steel wire mesh screens;
S3 is by the first powder calcination, and calcining heat is 1390 DEG C, calcination time 5h;
Strontium carbonate, silica the second microwave material of formation are added in the first powders of S4 after firing, in the second microwave
Deionized water is added in material and carries out ball milling, the second microwave material, deionized water, the quality of zirconia balls with zirconia balls
Than for 1: 1.2: 2.5, being dried after ball milling at 150 DEG C, then obtaining the second powder by 200 mesh steel wire mesh screens;
S5 is by the second powder calcination, and calcining heat is 1425 DEG C, calcination time 5h;
The second powder after calcining is put into polyesteramine bucket by S6, adds deionized water and zirconia balls, and the after calcining
Two powders, deionized water, the mass ratio of zirconia balls are 1: 1.0: 2.5, add polyvinyl alcohol water solution as binding agent, add
After entering dispersant and releasing agent ball milling 24h, it is granulated;
S7 is pressed into granulation powder the sequin of radius 13.85mm, thickness 6.2mm, and the compact density of sequin is
3.88g/cm3;
The sequin suppressed is sintered 20h at a temperature of 1650 DEG C and obtains product by S8.
Embodiment 1-3 is tested for the property, instrument model HP8703A, test cavity is 30 × t28mm's of Φ
Silver coated aluminum chamber, its each item data are as follows:
Present embodiment does not simply limit its protection domain to the exemplary illustration of this patent, and those skilled in the art are also
Local change can be carried out to it, as long as it does not exceed the essence of this patent, all be considered as the equivalent substitution to this patent, all
Within the protection domain of this patent.
Claims (10)
1. a kind of preparation method of low-k ultra high quality factor microwave-medium ceramics, it is characterised in that including following step
Suddenly,
S1 stocks up according to following molar ratio:0.15~0.25 barium carbonate;0.05~0.15 alundum (Al2O3);0.48~0.60 5 oxygen
Change two tantalums;0.15~0.22 zinc oxide;0.01~0.03 strontium carbonate;0.03~0.05 silica;
The barium carbonate, alundum (Al2O3), tantalum pentoxide, zinc oxide are mixed to form the first microwave material by S2, described
Deionized water is added in one microwave material and carries out ball milling with zirconia balls, is dried after ball milling, then by steel wire mesh screen
Obtain the first powder;
S3 is by first powder calcination;
The strontium carbonate, silica the second microwave material of formation are added in the first powders of S4 after firing, described second
Deionized water is added in microwave material and carries out ball milling with zirconia balls, dries after ball milling, is then obtained by steel wire mesh screen
To the second powder;
S5 is by second powder calcination;
The second powder after calcining is put into polyesteramine bucket by S6, adds deionized water and zirconia balls, adds polyvinyl alcohol water
Solution after adding dispersant and releasing agent ball milling 24h, is granulated as binding agent;
S7 is pressed into granulation powder the sequin of radius 13.85mm, thickness 6.2mm;
The sequin suppressed is sintered 20h at a temperature of 1600~1650 DEG C and obtains product by S8.
2. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S1, the barium carbonate, alundum (Al2O3), tantalum pentoxide, strontium carbonate, the purity of silica are
More than 99.99%.
3. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S2, first microwave material, deionized water, the mass ratio of zirconia balls are 1: 1.2: 2.5.
4. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S2, drying temperature is 150 ± 5 DEG C, and the steel wire mesh screen is 200 mesh.
5. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S3, calcining heat is 1350~1400 DEG C, calcination time 5h.
6. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S4, second microwave material, deionized water, the mass ratio of zirconia balls are 1: 1.2: 2.5.
7. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S4, drying temperature is 150 ± 5 DEG C, and the steel wire mesh screen is 200 mesh.
8. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S5, calcining heat is 1400~1450 DEG C, calcination time 5h.
9. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S6, the mass ratio of the second powder, deionized water, zirconia balls after calcining is 1: 1.0: 2.5.
10. the preparation method of low-k ultra high quality factor microwave-medium ceramics according to claim 1, its feature
It is, in the step S9, the compact density of the sequin is 3.90 ± 0.10g/cm3。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810014956.5A CN107935594A (en) | 2018-01-08 | 2018-01-08 | The preparation method of low-k ultra high quality factor microwave-medium ceramics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810014956.5A CN107935594A (en) | 2018-01-08 | 2018-01-08 | The preparation method of low-k ultra high quality factor microwave-medium ceramics |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107935594A true CN107935594A (en) | 2018-04-20 |
Family
ID=61937429
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810014956.5A Pending CN107935594A (en) | 2018-01-08 | 2018-01-08 | The preparation method of low-k ultra high quality factor microwave-medium ceramics |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107935594A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109020536A (en) * | 2018-09-29 | 2018-12-18 | 成都顺康三森电子有限责任公司 | A kind of media ceramic resonance manufacturing method |
CN109336597A (en) * | 2018-12-13 | 2019-02-15 | 张家港保税区灿勤科技有限公司 | The preparation method and test method of the base station 5G ceramic dielectric waveguide filter |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102659396A (en) * | 2012-03-28 | 2012-09-12 | 厦门松元电子有限公司 | Low-dielectric constant microwave ceramic dielectric material and preparation method thereof |
CN105669195A (en) * | 2016-01-04 | 2016-06-15 | 张家港保税区灿勤科技有限公司 | Low-dielectric-constant and high-Q-value microwave dielectric ceramic material and preparation method thereof |
-
2018
- 2018-01-08 CN CN201810014956.5A patent/CN107935594A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102659396A (en) * | 2012-03-28 | 2012-09-12 | 厦门松元电子有限公司 | Low-dielectric constant microwave ceramic dielectric material and preparation method thereof |
CN105669195A (en) * | 2016-01-04 | 2016-06-15 | 张家港保税区灿勤科技有限公司 | Low-dielectric-constant and high-Q-value microwave dielectric ceramic material and preparation method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109020536A (en) * | 2018-09-29 | 2018-12-18 | 成都顺康三森电子有限责任公司 | A kind of media ceramic resonance manufacturing method |
CN109336597A (en) * | 2018-12-13 | 2019-02-15 | 张家港保税区灿勤科技有限公司 | The preparation method and test method of the base station 5G ceramic dielectric waveguide filter |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104944939A (en) | Stable-temperature medium-temperature-sintering microwave dielectric ceramic and preparation method thereof | |
CN107235711B (en) | Temperature-stable metaantimmonic acid magnesium lithium-based microwave medium composite ceramics and preparation method thereof | |
CN104446468A (en) | X9R ceramic capacitor dielectric material and preparation method thereof | |
CN104961453A (en) | Temperature-stable type low-loss microwave dielectric ceramic and preparing method thereof | |
CN109020542A (en) | The preparation method of medium dielectric constant microwave medium ultra high quality factor microwave-medium ceramics | |
CN105801112A (en) | Nd and Al co-doped substituted Ba0.4Sr0.6TiO3 giant dielectric ceramic and preparation method thereof | |
JP2010285336A (en) | Sintered material for dielectric substance and method for producing the same, and sintered material for dielectric substance which has core-shell fine structure and method for producing the same | |
CN108314444A (en) | A kind of high q-factor rock salt class microwave dielectric material | |
CN107935594A (en) | The preparation method of low-k ultra high quality factor microwave-medium ceramics | |
CN109231985A (en) | A kind of preparation method of low-loss X8R type dielectric substance | |
CN107500754A (en) | It is a kind of to be used for high ceramic medium material for holding high pressure MLCC and preparation method thereof | |
CN108147809B (en) | Medium-low temperature sintered barium-titanium series microwave dielectric material and preparation method thereof | |
CN105669195B (en) | Low dielectric constant and high Q value microwave dielectric ceramic materials and preparation method thereof | |
CN104944940A (en) | Stable-temperature magnesium-titanate-base microwave dielectric ceramic and preparation method thereof | |
Sayyadi-Shahraki et al. | Microwave dielectric properties and chemical compatibility with silver electrode of Li2TiO3 ceramic with Li2O–ZnO–B2O3 glass additive | |
CN108218423A (en) | A kind of X8R types ceramic capacitor dielectric material and preparation method thereof | |
CN103396117A (en) | Low-temperature sintered strontium titanate energy-storing medium ceramic material and preparation method thereof | |
CN105399405B (en) | A kind of low dielectric microwave ferroelectric ceramics and preparation method thereof | |
CN104987070A (en) | Temperature stable microwave dielectric ceramic with medium dielectric constant and preparation method of temperature stable microwave dielectric ceramic | |
CN108395243B (en) | XnR BaTiO with wide temperature range and high stability3Base medium ceramic and preparation method thereof | |
CN104817322B (en) | A kind of temperature-stable capacitor ceramic material Sr4euTiNb9o30and preparation method thereof | |
CN109721359A (en) | A kind of lithium titanium is co-doped with high q-factor lithium magnesium niobium system dielectric material and preparation method thereof | |
CN113264763A (en) | Wide-temperature-stability barium titanate-based dielectric ceramic material and preparation method thereof | |
Lei et al. | Synthesis of (1− x) ZnAl2O4–xTiO2 microwave dielectric ceramics by molten-salt process | |
CN104710171B (en) | A kind of high energy storage density strontium bismuth titanate base complex phase ceramic and preparation method thereof |
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 | ||
CB02 | Change of applicant information |
Address after: 215634 Jiangsu Canqin Science and Technology Co., Ltd. No. 19 Jingang Road, Zhangjiagang Free Trade Zone, Suzhou City, Jiangsu Province Applicant after: Jiangsu Canqin Science and Technology Co., Ltd. Address before: Jingang road Suzhou 215634 Jiangsu province Zhangjiagang Free Trade Zone No. 19 Zhangjiagang bonded zone canqin science and Technology Co Ltd Applicant before: Zhangjiagang Bonded Area Canqin Technology Co., Ltd. |
|
CB02 | Change of applicant information | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180420 |
|
RJ01 | Rejection of invention patent application after publication |