CN103102168A - Preparation method of modified carbon fiber-reinforced composite ceramic - Google Patents
Preparation method of modified carbon fiber-reinforced composite ceramic Download PDFInfo
- Publication number
- CN103102168A CN103102168A CN2013100420037A CN201310042003A CN103102168A CN 103102168 A CN103102168 A CN 103102168A CN 2013100420037 A CN2013100420037 A CN 2013100420037A CN 201310042003 A CN201310042003 A CN 201310042003A CN 103102168 A CN103102168 A CN 103102168A
- Authority
- CN
- China
- Prior art keywords
- carbon fiber
- zno
- preparation
- modified carbon
- ceramic powder
- 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
Images
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
The invention provides a preparation method of modified carbon fiber-reinforced composite ceramic. The preparation method comprises the following steps: (1) placing carbon fiber into concentrated nitric acid, soaking and then washing with deionized water; (2) heating an ethanol solution of zinc acetate and the ethanol solution of NaOH to 65 DEG C, then mixing in equal molar ratio to prepare a ZnO sol; (3) dipping and lifting the carbon fiber in the ZnO sol for 2-3 times and pre-placing a ZnO crystal seed; (4) mixing a zinc salt solution and a hexamethylene tetramine solution in equal molar ratio to prepare a growth solution, placing the carbon fiber provided with the ZnO crystal seed into the growth solution, firstly performing heat preservation at the temperature of 80-90 DEG C, then washing, and drying to get a ZnO nano-wire array thin film growing on the carbon fiber in the fixed direction; (5) placing NiO and Fe2O3 on a planet mill for wet milling so as to form slurry, drying the slurry, and then pre-burning to get NiFe2O4-based ceramic powder; and (6) taking the NiFe2O4-based ceramic powder, additionally adding the short-cut carbon fiber after modification, performing dry pressing and forming, then placing into a multifunctional sintering furnace, and sintering under the protection of nitrogen to get the modified carbon fiber-reinforced composite ceramic.
Description
Technical field
The present invention relates to the preparation method that a kind of modified carbon fiber strengthens composite ceramics, belong to technical field of aluminum electrolysis.
Background technology
At present, the carbon annode material is still adopted in the conventional aluminum electrolysis, can discharge a large amount of greenhouse gases, contaminate environment in electrolytic process.And need the frequent anode material of changing, increase production cost.People are from energy-conservation and reduce production costs, and eliminate the electrolysis of aluminum pollution on the environment and set out, and Mathematical model has been produced some new designs.The investigator is being devoted to develop the aluminum electrolyzation technology that adopts the noble electrode system in the last thirty years, and its core is exactly the research of inert anode material.After the eighties in 20th century, the research of aluminum electrolysis inertia anode material mainly concentrates on metal anode, metal oxide anode, sintering metal anode.Metal anode is easy to make, and has good electroconductibility, therefore is considered always and makes the aluminium electrolysis anode material.But except some precious metal, metallic substance can not fully be resisted the oxygen corrosion of cryolite fused salt and electrolysis generation.Metal oxide is because unreactiveness receives much concern, but relatively poor electroconductibility and heat-shock resistance have limited again their application.Cermet material has been concentrated the unreactiveness of the good electron conduction of metallic substance and stupalith, so be considered to as the most promising material of inert anode always, the research of this respect is also maximum.But find in the electrolysis of aluminum experimental study, inert anode surface meeting produces a large amount of O
2Bubble, surface formed the gas shield film, stoped cryolite fused salt to the corrosion of inert anode and soaked into.Yet due to a large amount of O
2The fluctuation of bubble and electrolytic solution is washed away the inert anode surface, makes the ceramic matrix of cermet inert anode large-area cracking and slag-off phenomenon occur in electrolytic process, causes the electrolytic corrosion speed of inert anode material higher.Thereby the mechanical behavior under high temperature that how to improve the ceramic-base inert anode material becomes the key of inert anode research.
At present, the carbon fiber of employing high specific strength and high elastic coefficient has been subjected to the investigator mutually as ceramic toughening and has paid close attention to widely, and the interface performance of carbon fiber and ceramic matrix has determined the effect that fiber induces one, and affects to a great extent the fracture mode of matrix material.Often improve the interfacial state of carbon fiber and ceramic matrix by means of process for modifying surface such as high temperature oxidation alligatoring and metallizing coatings for this reason.But high-temperature oxidation process has greatly reduced original intensity of carbon fiber, and the wettability of metallic coating and ceramic matrix is bad, cause carbon fiber and ceramic matrix interface still to have more space, the suffered stress of ceramic matrix can not effectively be delivered on carbon fiber, so the mechanical property of ceramic matrix can not be improved.So, study a kind of coating technology oxide coated on carbon fiber, not reducing the original intensity of carbon fiber simultaneously is one of gordian technique of the carbon fiber-reinforced pottery of development.
Summary of the invention
The purpose of this invention is to provide the preparation method that a kind of modified carbon fiber that the composite ceramics density is high, intensity is large that can satisfy the demand, preparation strengthens composite ceramics.Its technical scheme is:
A kind of modified carbon fiber strengthens the preparation method of composite ceramics, and it is characterized in that adopting following steps: (1) cleans up carbon fiber to be placed on and soaks 5 ~ 8min in concentrated nitric acid, then removes the redundant nitric acid of surface attachment with washed with de-ionized water; (2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.01 ~ 0.2M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 1 ~ 2h, make stable ZnO colloidal sol; (3) carbon fiber is flooded 5 ~ 10min in ZnO colloidal sol, take out at 100 ~ 120 ℃ of drying 10 ~ 20min, dipping lifts 2 ~ 3 times repeatedly, presets the ZnO crystal seed on carbon fiber; (4) volumetric molar concentration being the zinc solution of 1～25mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 80 ~ 90 ℃ of insulation 2 ~ 8h, take out repetitive scrubbing, 70 ~ 100 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber, and wherein zinc solution is any in zinc nitrate, zinc sulfate or zinc chloride; (5) adopt NiO and Fe
2O
3Be starting material, be placed on planetary mills and form slip after wet-milling 10 ~ 20min, with putting into 1000 ~ 1100 ℃ of pre-burning 4 ~ 6h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtain NiFe
2O
4The based ceramic powder material; (6) get NiFe
2O
4The based ceramic powder material separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material quality 2 ~ 5%; carbon fiber length is 2 ~ 5mm; after mixing, 25 ~ 100MPa is dry-pressing formed; then put into multifunctional sintering furnace; under nitrogen protection; in 1300 ~ 1350 ℃ of sintering 5 ~ 8h, obtain ZnO nano-wire surface modified carbon fiber reinforcement ferronickel spinel composite ceramics.
Described a kind of modified carbon fiber strengthens the preparation method of composite ceramics, in step (5), separately adds the additive of starting material total mass 2 ~ 3%, together is placed in wet-milling formation slip on planetary mills with starting material, and additive is MnO
2, V
2O
5And TiO
2In a kind of or any two mixing.
Described a kind of modified carbon fiber strengthens the preparation method of composite ceramics, in step (5), and NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio.
Described a kind of modified carbon fiber strengthens the preparation method of composite ceramics, in step (6), and NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, and the chopped carbon fiber of getting after minus mesh and modification adopts the dry method batch mixing, at this moment non-grinding medium.
Described a kind of modified carbon fiber strengthens the preparation method of composite ceramics, in step (6), and NiFe
2O
4After chopped carbon fiber batch mixing after based ceramic powder material and modification, separately add the binding agent of mixture total mass 5% and mix, dry-pressing formed, wherein binding agent is any in polyvinyl alcohol or methylcellulose gum.
Described a kind of modified carbon fiber strengthens the preparation method of composite ceramics, and in step (6), the temperature rise rate of multifunctional sintering furnace is 3 ℃/min, after 1300 ~ 1350 ℃ of insulation 5 ~ 8h, and furnace cooling.
The present invention compared with prior art, its advantage is:
1, pass through carbon fiber surface modification, use directly growing ZnO nano-wire on carbon fiber of liquid phase deposition, form carbon fiber/ZnO matrix material, pyroprocessing oxidation or existing cycle of chemical plating technology have been overcome in existing carbon fiber treatment technology long, the shortcoming that microtexture is restive, reduce the original intensity of carbon fiber.
2, adopt carbon fiber/ZnO matrix material to add NiFe to as wild phase
2O
4In the base ceramic phase, improved the interface structure of carbon fiber with the ceramic matrix phase, increase its interface binding power, and ZnO uniform particles, disperse are distributed in the ceramic particle interface, strengthened boundary strength, promote sintering, overcome the shortcoming that in existing nano particle toughening technology, nanoparticle is easily reunited, made density, heat-shock resistance and the bending strength of ZnO nano-wire surface modified carbon fiber reinforcement ferronickel spinel composite ceramics all greatly improve.
Description of drawings
Fig. 1 is the SEM figure of the embodiment of the present invention 1 gained ZnO nano-wire surface modified carbon fiber reinforcement ferronickel spinel composite ceramics section;
Fig. 2 is the SEM figure of pure nickel hercynite base pottery section.
Embodiment
Embodiment 1, and its concrete steps are:
(1) carbon fiber is cleaned up be placed on and soak 5min in concentrated nitric acid, then remove the redundant nitric acid of surface attachment with washed with de-ionized water;
(2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.01M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 1h, make stable ZnO colloidal sol;
(3) carbon fiber is flooded 10min in ZnO colloidal sol, take out at 120 ℃ of dry 10min, then dipping lifts 2 times repeatedly, presets the ZnO crystal seed on carbon fiber;
(4) volumetric molar concentration being the zinc nitrate solution of 12mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 90 ℃ of insulation 4h, take out repetitive scrubbing, 90 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber;
(5) adopt NiO and Fe
2O
3Be starting material, NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio, is placed on planetary mills and forms slip after wet-milling 20min, with putting into 1100 ℃ of pre-burning 6h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtains NiFe
2O
4The based ceramic powder material;
(6) with NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material screen blanking quality 2%; carbon fiber length is 5mm; separately add the polyvinyl alcohol adhesive of mixture total mass 5% and mix after adopting the dry method batch mixing; dry-pressing formed in 60MPa; sample size is the Cylindrical Samples of Φ 50 * 15 ± 2mm; then put into multifunctional sintering furnace; under nitrogen protection; temperature rise rate is 3 ℃/min; in 1300 ℃ of sintering 5h; furnace cooling obtains the spinel based composite ceramics of ZnO nano-wire surface modified carbon fiber reinforcement ferronickel.
With target compound of the present invention and the pure nickel hercynite base pottery contrast of not adding modified carbon fiber, evidence: the density of composite ceramics of the present invention, heat-shock resistance and bending strength improve respectively 19%, 250% and 70% than pure nickel hercynite base pottery, and mechanical property strengthens greatly.
Embodiment 2:
(1) carbon fiber is cleaned up be placed on and soak 8min in concentrated nitric acid, then remove the redundant nitric acid of surface attachment with washed with de-ionized water;
(2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.2M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 2h, make stable ZnO colloidal sol;
(3) carbon fiber is flooded 5min in ZnO colloidal sol, take out at 100 ℃ of dry 20min, then dipping lifts 2 times repeatedly, presets the ZnO crystal seed on carbon fiber;
(4) volumetric molar concentration being the solution of zinc sulfate of 1mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 80 ℃ of insulation 2h, take out repetitive scrubbing, 70 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber;
(5) adopt NiO and Fe
2O
3Be starting material, NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio, separately adds the MnO of starting material total mass 2%
2Additive is placed on planetary mills and forms slip after wet-milling 10min, with putting into 1000 ℃ of pre-burning 4h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtains NiFe
2O
4The based ceramic powder material;
(6) with NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material screen blanking quality 5%; carbon fiber length is 2mm; separately add the methyl cellulose binder of mixture total mass 5% and mix after adopting the dry method batch mixing; dry-pressing formed in 25MPa; sample size is the Cylindrical Samples of Φ 50 * 20 ± 2mm; then put into multifunctional sintering furnace; under nitrogen protection; temperature rise rate is 3 ℃/min; in 1300 ℃ of sintering 8h; furnace cooling obtains the spinel based composite ceramics of ZnO nano-wire surface modified carbon fiber reinforcement ferronickel.
Embodiment 3:
(1) carbon fiber is cleaned up be placed on and soak 6min in concentrated nitric acid, then remove the redundant nitric acid of surface attachment with washed with de-ionized water;
(2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.1M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 1.5h, make stable ZnO colloidal sol;
(3) carbon fiber is flooded 7min in ZnO colloidal sol, take out at 110 ℃ of dry 15min, then dipping lifts 1 time, preset the ZnO crystal seed on carbon fiber;
(4) volumetric molar concentration being the liquor zinci chloridi of 25mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 85 ℃ of insulation 8h, take out repetitive scrubbing, 100 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber;
(5) adopt NiO and Fe
2O
3Be starting material, NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio, separately adds the additive of starting material total mass 3%, and additive is MnO
2With V
2O
5Wait mass mixing, be placed in and form slip on planetary mills after wet-milling 15min, will put into 1100 ℃ of pre-burning 5h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtain NiFe
2O
4The based ceramic powder material;
(6) with NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material screen blanking quality 5%; carbon fiber length is 4mm; separately add the methyl cellulose binder of mixture total mass 5% and mix after adopting the dry method batch mixing; dry-pressing formed in 100MPa; sample size is the Cylindrical Samples of Φ 100 * 40 ± 5mm; then put into multifunctional sintering furnace; under nitrogen protection; temperature rise rate is 3 ℃/min; in 1300 ℃ of sintering 6h; furnace cooling obtains the spinel based composite ceramics of ZnO nano-wire surface modified carbon fiber reinforcement ferronickel.
Embodiment 4:
(1) carbon fiber is cleaned up be placed on and soak 8min in concentrated nitric acid, then remove the redundant nitric acid of surface attachment with washed with de-ionized water;
(2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.1M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 2h, make stable ZnO colloidal sol;
(3) carbon fiber is flooded 5min in ZnO colloidal sol, take out at 100 ℃ of dry 20min, then dipping lifts 2 times repeatedly, presets the ZnO crystal seed on carbon fiber;
(4) volumetric molar concentration being the solution of zinc sulfate of 10mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 85 ℃ of insulation 3h, take out repetitive scrubbing, 80 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber;
(5) adopt NiO and Fe
2O
3Be starting material, NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio, separately adds the TiO of starting material total mass 2.5%
2Additive is placed on planetary mills and forms slip after wet-milling 10min, with putting into 1100 ℃ of pre-burning 4h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtains NiFe
2O
4The based ceramic powder material;
(6) with NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material screen blanking quality 3%; carbon fiber length is 2mm; separately add the polyvinyl alcohol adhesive of mixture total mass 5% and mix after adopting the dry method batch mixing; dry-pressing formed in 40MPa; sample size is the Cylindrical Samples of Φ 50 * 18 ± 2mm; then put into multifunctional sintering furnace; under nitrogen protection; temperature rise rate is 3 ℃/min; in 1350 ℃ of sintering 5h; furnace cooling obtains the spinel based composite ceramics of ZnO nano-wire surface modified carbon fiber reinforcement ferronickel.
Claims (6)
1. a modified carbon fiber strengthens the preparation method of composite ceramics, and it is characterized in that adopting following steps: (1) cleans up carbon fiber to be placed on and soaks 5 ~ 8min in concentrated nitric acid, then removes the redundant nitric acid of surface attachment with washed with de-ionized water; (2) volumetric molar concentration is the zinc acetate ethanolic soln of 0.01 ~ 0.2M and NaOH ethanolic soln and is heated to separately 65 ℃ after equimolar ratio mix, stir 1 ~ 2h, make stable ZnO colloidal sol; (3) carbon fiber is flooded 5 ~ 10min in ZnO colloidal sol, take out at 100 ~ 120 ℃ of drying 10 ~ 20min, dipping lifts 2 ~ 3 times repeatedly, presets the ZnO crystal seed on carbon fiber; (4) volumetric molar concentration being the zinc solution of 1～25mM and hexamethylenetetramine solution etc. mole pours in beaker, mix and make growth media, the carbon fiber that presets the ZnO crystal seed is put into growth media together be placed in again water-bath, at 80 ~ 90 ℃ of insulation 2 ~ 8h, take out repetitive scrubbing, 70 ~ 100 ℃ of dryings again can obtain the ZnO nanowire array film of oriented growth on carbon fiber, and wherein zinc solution is any in zinc nitrate, zinc sulfate or zinc chloride; (5) adopt NiO and Fe
2O
3Be starting material, be placed on planetary mills and form slip after wet-milling 10 ~ 20min, with putting into 1000 ~ 1100 ℃ of pre-burning 4 ~ 6h of high temperature resistance furnace after 110 ℃ of oven dry of slip, obtain NiFe
2O
4The based ceramic powder material; (6) get NiFe
2O
4The based ceramic powder material separately adds NiFe
2O
4Chopped carbon fiber after the modification of based ceramic powder material quality 2 ~ 5%; carbon fiber length is 2 ~ 5mm; after mixing, 25 ~ 100MPa is dry-pressing formed; then put into multifunctional sintering furnace; under nitrogen protection; in 1300 ~ 1350 ℃ of sintering 5 ~ 8h, obtain ZnO nano-wire surface modified carbon fiber reinforcement ferronickel spinel composite ceramics.
2. a kind of modified carbon fiber as claimed in claim 1 strengthens the preparation method of composite ceramics, it is characterized in that: in step (5), separately add the additive of starting material total mass 2 ~ 3%, together be placed in wet-milling formation slip on planetary mills with starting material, additive is MnO
2, V
2O
5And TiO
2In a kind of or any two mixing.
3. a kind of modified carbon fiber as claimed in claim 1 strengthens the preparation method of composite ceramics, it is characterized in that: in step (5), and NiO and Fe
2O
3Raw material is the 1.5:1 batching in molar ratio.
4. a kind of modified carbon fiber as claimed in claim 1 strengthens the preparation method of composite ceramics, it is characterized in that: in step (6), and NiFe
2O
4The based ceramic powder material is the standard sieve screening of 0.038mm by grinding by the aperture, and the chopped carbon fiber of getting after minus mesh and modification adopts the dry method batch mixing, at this moment non-grinding medium.
5. a kind of modified carbon fiber as claimed in claim 1 strengthens the preparation method of composite ceramics, it is characterized in that: in step (6), and NiFe
2O
4After chopped carbon fiber batch mixing after based ceramic powder material and modification, separately add the binding agent of mixture total mass 5% and mix, dry-pressing formed, wherein binding agent is any in polyvinyl alcohol or methylcellulose gum.
6. a kind of modified carbon fiber as claimed in claim 1 strengthens the preparation method of composite ceramics, and it is characterized in that: in step (6), the temperature rise rate of multifunctional sintering furnace is 3 ℃/min, after 1300 ~ 1350 ℃ of insulation 5 ~ 8h, and furnace cooling.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2013100420037A CN103102168A (en) | 2013-02-02 | 2013-02-02 | Preparation method of modified carbon fiber-reinforced composite ceramic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2013100420037A CN103102168A (en) | 2013-02-02 | 2013-02-02 | Preparation method of modified carbon fiber-reinforced composite ceramic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN103102168A true CN103102168A (en) | 2013-05-15 |
Family
ID=48310407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2013100420037A Pending CN103102168A (en) | 2013-02-02 | 2013-02-02 | Preparation method of modified carbon fiber-reinforced composite ceramic |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103102168A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103590234A (en) * | 2013-11-28 | 2014-02-19 | 哈尔滨工业大学 | Preparation method for zinc oxide nanowire-modified PBO fiber |
| CN103628305A (en) * | 2013-11-28 | 2014-03-12 | 哈尔滨工业大学 | Zinc oxide nanowire modified PBO (Poly-p-phenylenebenzobisthiazole) fiber |
| CN105421084A (en) * | 2015-12-04 | 2016-03-23 | 镇江奥立特机械制造有限公司 | Novel fiber liquid-immersing method |
| CN105413672A (en) * | 2015-11-25 | 2016-03-23 | 天津中材工程研究中心有限公司 | Nano-zinc oxide and carbon fiber composite material and preparation method thereof |
| CN106147117A (en) * | 2016-06-29 | 2016-11-23 | 陕西科技大学 | On carbon cloth, growing zinc oxide nanorod strengthens the preparation method of resin-matrix friction material |
| CN106892677A (en) * | 2017-02-20 | 2017-06-27 | 佛山市蓝瑞欧特信息服务有限公司 | A kind of carbon fiber ceramic material and preparation method thereof |
| CN109054084A (en) * | 2018-07-20 | 2018-12-21 | 安徽锦华氧化锌有限公司 | A kind of rubber modified zinc oxide-carbon fiber composite fibre and preparation method thereof |
| CN110318252A (en) * | 2019-08-16 | 2019-10-11 | 四川轻化工大学 | Composite material with spiral carbon nanofiber surface loaded with zinc oxide particles and preparation method and application thereof |
| CN110835269A (en) * | 2019-10-30 | 2020-02-25 | 安徽朗基新材料科技有限公司 | Production process of high-strength high-performance soft magnetic ferrite material |
| CN114433147A (en) * | 2022-02-26 | 2022-05-06 | 广东工业大学 | Preparation method of carbon cloth loaded zinc oxide/silver phosphate composite photocatalytic material |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101041887A (en) * | 2007-04-27 | 2007-09-26 | 刘春祥 | Boracic acid aluminium crystal whisker/casting aluminum alloy composite material and preparation method thereof |
| CN101805174A (en) * | 2010-04-08 | 2010-08-18 | 长沙理工大学 | NiFe prepared by chemical coprecipitation method2O4Method for preparing spinel ceramic powder |
-
2013
- 2013-02-02 CN CN2013100420037A patent/CN103102168A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101041887A (en) * | 2007-04-27 | 2007-09-26 | 刘春祥 | Boracic acid aluminium crystal whisker/casting aluminum alloy composite material and preparation method thereof |
| CN101805174A (en) * | 2010-04-08 | 2010-08-18 | 长沙理工大学 | NiFe prepared by chemical coprecipitation method2O4Method for preparing spinel ceramic powder |
Non-Patent Citations (2)
| Title |
|---|
| ULISES GALAN ET AL.: ""Effect of ZnO nanowire morphology on the interfacial strength of nanowire coated carbon fibers"", 《COMPOSITES SCIENCE AND TECHNOLOGY》 * |
| XIULI LONG ET AL.: ""Effect of adding fiber on the microstructure and mechanical properties of NiFe2O4 composite ceramics"", 《CERAMICS INTERNATIONAL》 * |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103590234A (en) * | 2013-11-28 | 2014-02-19 | 哈尔滨工业大学 | Preparation method for zinc oxide nanowire-modified PBO fiber |
| CN103628305A (en) * | 2013-11-28 | 2014-03-12 | 哈尔滨工业大学 | Zinc oxide nanowire modified PBO (Poly-p-phenylenebenzobisthiazole) fiber |
| CN103590234B (en) * | 2013-11-28 | 2015-08-19 | 哈尔滨工业大学 | A kind of preparation method of zinc oxide nanowire modification pbo fiber |
| CN103628305B (en) * | 2013-11-28 | 2016-02-17 | 哈尔滨工业大学 | A kind of pbo fiber of zinc oxide nanowire modification |
| CN105413672A (en) * | 2015-11-25 | 2016-03-23 | 天津中材工程研究中心有限公司 | Nano-zinc oxide and carbon fiber composite material and preparation method thereof |
| CN105421084A (en) * | 2015-12-04 | 2016-03-23 | 镇江奥立特机械制造有限公司 | Novel fiber liquid-immersing method |
| CN106147117A (en) * | 2016-06-29 | 2016-11-23 | 陕西科技大学 | On carbon cloth, growing zinc oxide nanorod strengthens the preparation method of resin-matrix friction material |
| CN106147117B (en) * | 2016-06-29 | 2018-06-19 | 陕西科技大学 | The preparation method of growing zinc oxide nanorod reinforced resin base frication material on carbon cloth |
| CN106892677A (en) * | 2017-02-20 | 2017-06-27 | 佛山市蓝瑞欧特信息服务有限公司 | A kind of carbon fiber ceramic material and preparation method thereof |
| CN109054084A (en) * | 2018-07-20 | 2018-12-21 | 安徽锦华氧化锌有限公司 | A kind of rubber modified zinc oxide-carbon fiber composite fibre and preparation method thereof |
| CN109054084B (en) * | 2018-07-20 | 2020-08-11 | 安徽锦华氧化锌有限公司 | Modified zinc oxide-carbon fiber composite fiber for rubber and preparation method thereof |
| CN110318252A (en) * | 2019-08-16 | 2019-10-11 | 四川轻化工大学 | Composite material with spiral carbon nanofiber surface loaded with zinc oxide particles and preparation method and application thereof |
| CN110835269A (en) * | 2019-10-30 | 2020-02-25 | 安徽朗基新材料科技有限公司 | Production process of high-strength high-performance soft magnetic ferrite material |
| CN114433147A (en) * | 2022-02-26 | 2022-05-06 | 广东工业大学 | Preparation method of carbon cloth loaded zinc oxide/silver phosphate composite photocatalytic material |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103102168A (en) | Preparation method of modified carbon fiber-reinforced composite ceramic | |
| CN104973662B (en) | Oxide anode for treatment of ship domestic sewage and preparation method thereof | |
| CN104562128B (en) | A kind of method for preparing thermal protection ceramic layer on metal or metallic composite surface | |
| CN105244191A (en) | Manganese cobalt oxide porous nanometer sheet/foam nickel compound electrode material preparation method | |
| CN103908969B (en) | A kind of BiFeO 3nano-particles reinforcement TiO 2the preparation method of nanometer pipe array electrode material | |
| CN105244192A (en) | Magnesium cobaltite porous nanowire array/ nickel foam composite electrode material preparation method | |
| CN102051634A (en) | Titanium electrode material with porous titanium as substrate and preparation method of titanium electrode material | |
| CN106277042B (en) | One kind prepares Ti4O7Method | |
| CN104894595A (en) | High-catalytic-activity amorphous metal oxide hydrogen evolution electrode and preparation method thereof | |
| CN104532290B (en) | A kind of Fe2O3/ ZnO homojunction materials and its production and use | |
| CN108130582A (en) | A kind of preparation method of 2.5 dimension anodes of high catalytic activity carried magnetic particle | |
| CN103014755A (en) | Fabrication method of long-life titanium base electrode | |
| CN103253672A (en) | Preparation method of silicon carbide nanowire thin film based on hydrogen production by photoelectric catalytic decomposition of water | |
| Li et al. | Electrochemical properties of powder-pressed Pb–Ag–PbO2 anodes | |
| Li et al. | Homogeneous nanosheet Co 3 O 4 film prepared by novel unipolar pulse electro-deposition method for electrochemical water splitting | |
| CN105336503A (en) | Preparation method of copper cobaltate porous microrod and nickel foam composite electrode material | |
| CN105161319B (en) | The preparation method of Nano tube array of titanium dioxide nickel-loaded cobalt oxide electrode material | |
| CN106683896A (en) | Preparation method and application of core-shell-structured nickel molybdate/manganese dioxide composite material | |
| CN103305866A (en) | Preparation method of iridium oxide nanometer coating electrode taking aluminum oxide-based composite material as base body | |
| CN101285206B (en) | Preparation method for zinc bloom and zinc aluminate composite nano-tubes and arrays | |
| CN113584422B (en) | Surface Ti of metal titanium bipolar plate of proton exchange membrane fuel cell 4 O 7 Method for producing a coating | |
| CN110052601A (en) | A kind of method of the modified AB5 type hydrogen storage alloy of silica-graphene compound coating | |
| CN113529133B (en) | Preparation method of self-supporting type bifunctional catalytic electrode | |
| CN108660443B (en) | Preparation method and application of stannic oxide electrode | |
| CN114808041A (en) | Preparation and activation regeneration method of Pb-based pseudomorphic stable anode for manganese electrodeposition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WD01 | Invention patent application deemed withdrawn after publication | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130515 |