High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for...High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for high-resistivity SiC single crystal growth, the preparation technology of SiC powder is different from that of SiC ceramic. The influence of the shape and size of carbon particles on the morphology and phase composition of the obtained SiC powder were discussed. The phase composition and morphology of the products were investigated by X-ray diffraction, Raman microspectroscopy and scanning electron microscopy. The results show that the composition of resulting SiC by in-situ synthesis from Si/C mixture strongly depends on the nature of the carbon source, which corresponds to the particle size and shape, as well as the preparation temperature. In the experimental conditions, flake graphite is more suitable for the synthesis of SiC powder than activated carbon because of its relatively smaller particle size and flake shape, which make the conversion more complete. The major phase composition of the full conversion products is β-SiC, with traces of α-SiC. Glow discharge mass spectroscopy measurements indicated that SiC powder synthesized with this chemical reaction method can meet the purity demand for the growth of high-resistivity SiC single crystals.展开更多
The dielectric properties of nano Si/C/N composite powder and nano SiC powder at high frequencies have been studied. The nano Si/C/N composite powder and nano SiC powder were synthesized from hexamethyldisilazane ((Me...The dielectric properties of nano Si/C/N composite powder and nano SiC powder at high frequencies have been studied. The nano Si/C/N composite powder and nano SiC powder were synthesized from hexamethyldisilazane ((Me 3Si) 2NH) (Me:CH 3) and SiH 4 C 2H 2 respectively by a laser induced gas phase reaction. The complex permittivities of the nano Si/C/N composite powder and nano SiC powder were measured between 8 2GHz and 12 4GHz. The real and imaginary parts of the complex permittivities of nano Si/C/N composite powder are much higher than those of nano SiC powder. The SiC microcrystalline in the nano Si/C/N composite powder dissolved a great deal of nitrogen. The local structure around Si atoms changed by introducing N into SiC. Carbon atoms around Si were substituted by N atoms. So charged defects and quasi free electrons moved in response to the electric field, diffusion or polarization current resulted from the field propagation. The high ε″and loss factor tgδ(ε″/ε′) of Si/C/N composite powder were due to the dielectric relaxation.展开更多
Phase pure ZrB2-SiC composite powders were prepared after 1 450℃/3 h via carbothermal reduction route,by using ZrSiO4,B2O3 and carbon as the raw materials.The influences of firing temperature as well as the type and ...Phase pure ZrB2-SiC composite powders were prepared after 1 450℃/3 h via carbothermal reduction route,by using ZrSiO4,B2O3 and carbon as the raw materials.The influences of firing temperature as well as the type and amount of additive on the phase composition of final products were detailedly investigated.The results indicated that the onset formation temperature of ZrB2-SiC was reduced to 1 400℃by the present conditions,and oxide additive（including CoSO4·7H2O,Y2O3 and TiO2）was effective in enhancing the decomposition of raw ZrSiO4,therefore accelerating the synthesis of ZrB2-SiC.Moreover,microstructural observation showed that the as-prepared ZrB2 and SiC respectively had well-defined hexagonal columnar and fibrous morphology.Furthermore,the methodology of back-propagation artificial neural networks（BP-ANNs）was adopted to establish a model for predicting the reaction extent（e g,the content of ZrB2-SiC in final product）in terms of various processing conditions.The results predicted by the as-established BP-ANNs model matched well with that of testing experiment（with a mean square error in 10^（-3） degree）,verifying good effectiveness of the proposed strategy.展开更多
Nano-SiC powders doped by B were synthesized through the carbothermal reduction of xerogels containing the tributyl borate. The results show that the 3C-SiC with minor phase of 6H-SiC is generated at 1 700 ℃,and that...Nano-SiC powders doped by B were synthesized through the carbothermal reduction of xerogels containing the tributyl borate. The results show that the 3C-SiC with minor phase of 6H-SiC is generated at 1 700 ℃,and that there are not the characteristic peaks of any boride in the XRD patterns,which indicates that the boron is available only on the crystallization of 3C-SiC. The Raman spectra of the samples also show the characteristic bands of 3C-and 6H-SiC at 788 and 965 cm-1. But the bands at 1 345 and 1 590 cm-1 are characteristic peaks of amorphous carbon materials. The intensities of peaks at 788 and 965 cm-1 increase with B content in Raman spectra,which also shift to higher wavenumber with the increasing B. The microstructure of SiC powder is composed of agglomerated particles with diameters ranging from 30 to 100 nm. The results of dielectric property show that the sample with 0.005 B has the largest values in ε′ and ε″ among the four samples due to the existence of the intrinsic defects. But the absence of the relaxation polarization leads to low values of all the samples.展开更多
The aging-hardening kinetics of powder metallurgy processed 2014Al alloy and its composite have been studied. The existence of n-SiC particulates leads to the increase of peak hardness. Interestingly, the aginghardeni...The aging-hardening kinetics of powder metallurgy processed 2014Al alloy and its composite have been studied. The existence of n-SiC particulates leads to the increase of peak hardness. Interestingly, the aginghardening peak of the composite takes place at earlier time than that of the unreinforced alloy. Transmission electron microscopy（TEM） studies indicated that the major precipitation phases are Al_5Cu_2Mn_3 and θ′（Al_2Cu）. Besides, Ω phase appeared in both specimens at peak hardening condition, which has been rarely observed previously in aluminum metal matrix composites without Ag. Accelerated aging kinetics and increased peak hardness may be attributed to the higher dislocation density resulted from the mismatch of coefficients of thermal expansion between n-SiC and 2014Al matrix. The results are beneficial to fabricating high performance composites for the application in automobile field such as pistons, driveshaft tubes, brake rotors, bicycle frames, railroad brakes.展开更多
Fabrication of silicon carbide(SiC)ceramics by digital light processing(DLP)technology is difficult owing to high refractive index and high ultraviolet(UV)absorptivity of SiC powders.The surface of the SiC powders can...Fabrication of silicon carbide(SiC)ceramics by digital light processing(DLP)technology is difficult owing to high refractive index and high ultraviolet(UV)absorptivity of SiC powders.The surface of the SiC powders can be coated with silicon oxide(SiO_(2))with low refractive index and low UV absorptivity via high-temperature oxidation,reducing the loss of UV energy in the DLP process and realizing the DLP preparation of the SiC ceramics.However,it is necessary to explore a high-temperature modification process to obtain a better modification effect of the SiC powders.Therefore,the high-temperature modification behavior of the SiC powders is thoroughly investigated in this paper.The results show that nano-scale oxide film is formed on the surface of the SiC powders by short-time high-temperature oxidation,effectively reducing the UV absorptivity and the surface refractive index(nʹ)of the SiC powders.When the oxidation temperature is 1300℃,compared with that of unoxidized SiC powders,the UV absorptivity of oxidized SiC powders decreases from 0.5065 to 0.4654,and a curing depth of SiC slurry increases from 22±4 to 59±4μm.Finally,SiC green bodies are successfully prepared by the DLP with the the oxidized powders,and flexural strength of SiC sintered parts reaches 47.9±2.3 MPa after 3 h of atmospheric sintering at 2000℃without any sintering aid.展开更多
ZrO2-SiC composite powder was synthesized by carbothermal reduction of zircon in argon atmosphere, and it was used as the additive to prepare Al2O3-C refractories. The effects of heating temperature on the synthesis p...ZrO2-SiC composite powder was synthesized by carbothermal reduction of zircon in argon atmosphere, and it was used as the additive to prepare Al2O3-C refractories. The effects of heating temperature on the synthesis process and the addition of the synthesized composite powder on the properties of the Al2O3-C refractories were investigated. The results show that the synthesized composite powder can be easily obtained by heating the mixture of zircon and carbon black at 1 873 K for 4 h in argon atmosphere, and the relative contents of ZrO2 and SiC in sample reach about 83.7% and 16.3%, respectively. The bulk density, crushing strength and thermal shock resistance of the Al2O3-C refractories can be improved obviously by the addition of the synthesized ZrO2-SiC composite powder.展开更多
SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase forma...SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase formation, and the thermodynamic analysis was performed systematically. Moreover, the variation of its microwave permittivity with different atomic ratio of Al/Si was investigated in the frequency range of 8.2-12.4 GHz. The results show that, the powder obtained consists of spherical particles of 300-400 nm in diameter, which are composed of SiC and Al2O3 microcrystal with the grain size of approximately 45 nm. The results of XRD accord with those of the thermodynamic analysis. It is impossible for Al atoms to dissolve in the lattice of SiC during the carbothermal reduction process. Along with the increase of atomic ratio of Al/Si in the xerogel, the amount of Al2O3 in the powder synthesized increases, which reduces bothε', the real part of complex permittivity, and tgδ(ε'/ε'), the dissipation factor, whereε' is the imaginary part of complex permittivity.展开更多
The properties of SiC kiln furniture bonded with fine silicon powderare related to the bonder’s crystal structure. At high temperature, it will crystallize ina-cristobalite with great bulk effect. MnO2 mineralizer ca...The properties of SiC kiln furniture bonded with fine silicon powderare related to the bonder’s crystal structure. At high temperature, it will crystallize ina-cristobalite with great bulk effect. MnO2 mineralizer can make a-cristobalite convertto a-tridymite whose bulk effect is small. The crystal structure and its amount were investigated with XRD technique. The influence of different amounts of MnO2 on thecrystal structure and polycrystal transformation, and that of crystal structure on theproperties of kiln furniture were studied. The best proportion of MnO2 added was determined to be 2.0%.展开更多
Co-SiC core-shell powders were prepared by electroless plating. Scanning electron microscopy （SEM） revealed that Co-SiC core-shell powders were of nearly sphere-like shape and were about 0.3 pan. X-ray powder diffra...Co-SiC core-shell powders were prepared by electroless plating. Scanning electron microscopy （SEM） revealed that Co-SiC core-shell powders were of nearly sphere-like shape and were about 0.3 pan. X-ray powder diffraction （XRD） patterns showed that the cobalt powder was hexagonal crystallite. The complex dielectric constant and the complex permeability of Co-SiC core-shell powders-paraffin wax composite were measured by the rectangle wavegnide method. It showed that the dielectric loss was less than 0.1 and the magnetic loss was about 0.2 in 8.2-12.4 GHz for prepared Co-SiC core-shell comoosite oowders.展开更多
Nickel oxide (NiO) powder is prepared by decomposition of basic nickel carbonate (mNiCO3.nNi(OH)2.xH2O) (BNC) in microwave field with silicon carbide (SiC) as an indirect heating medium. The decomposition proceeds sta...Nickel oxide (NiO) powder is prepared by decomposition of basic nickel carbonate (mNiCO3.nNi(OH)2.xH2O) (BNC) in microwave field with silicon carbide (SiC) as an indirect heating medium. The decomposition proceeds stage by stage: firstly BNC removes its crystal water with the heat provided by BNC itself and SiC which absorb microwave energy,then removes CO2 and H2O from the anhydride (mNiCO3 .nNi(OH)2) and begins to produce NiO with the heat provided by SiC, and finally decomposes into NiO powder completely with the heat provided by the produced NiO which absorbs microwave energy strongly. In the microwave irradiation process, the decomposition of BNC can be accelerated by increasing the amount of BNC, the amount of SiC and the microwave field power. The size of the NiO granule is about 18ourn when the size of BNC used is about 15ourn.展开更多
β-SiC nanoparticle reinforced A1 matrix （nano-SiCp/A1） composite was prepared by a multi- step powder metallurgy strategy including presureless sintering, hot compacting process and hot extrusion. The microstructur...β-SiC nanoparticle reinforced A1 matrix （nano-SiCp/A1） composite was prepared by a multi- step powder metallurgy strategy including presureless sintering, hot compacting process and hot extrusion. The microstructures of the as-prepared composites were observed by scanning electronic microscopy （SEM）, and the mechanical properties were characterized by tensile strength measurement and Brinell hardness test. The experimental results revealed that the tensile strength of the composite with the addition of 5wt%/3-SIC nanoprtieles could be increased to 215 MPa, increasing by 110% compared with pure A1 matrix. Comparative experiments reflected that theβ-SIC nanoprticles showed significant reinforcement effect than traditional a-SiC micro-sized particles. The preparation process and sintering procedure were investigated to develop a cost effective preparation strategy to fabricate nano-SiCp/A1 composite.展开更多
Low cost silicon carbon nanometer powder was synthesized by carbothermal reduction method with nanometer SiO2 and carbon as raw material. Its synthesis thermodynamics were discussed. The influence of La on TG-DSC curv...Low cost silicon carbon nanometer powder was synthesized by carbothermal reduction method with nanometer SiO2 and carbon as raw material. Its synthesis thermodynamics were discussed. The influence of La on TG-DSC curve was also analyzed. It indicated that the synthesis process of SiC powder had two steps. In the first step two medial productions of SiOg and COg formed, and in the second step, β-SiC was finally synthesized. After 0.3% La added, at the first step, the initiatory forming temperature of producing SiO(g) and CO(g) declined from 1351.4 to 1250.9 ℃, and the thermal activation energy decreased from 223.6 to 34.7 J·g-1; at the second step the initiatory forming temperature of synthesizing β-SiC powder declined from 1526.5 to 1357.8 ℃, and the thermal activation energy decreased from 693.7 to 295.7 J·g-1. Without La added, the best synthesis technology for β-SiC powder was 1550 ℃ for 120 min, average powder diameter was bigger about 150 nm. With La added, the best synthesis technology was 1500 ℃ for 120 min, average powder diameter was about 100 nm.展开更多
文摘High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for high-resistivity SiC single crystal growth, the preparation technology of SiC powder is different from that of SiC ceramic. The influence of the shape and size of carbon particles on the morphology and phase composition of the obtained SiC powder were discussed. The phase composition and morphology of the products were investigated by X-ray diffraction, Raman microspectroscopy and scanning electron microscopy. The results show that the composition of resulting SiC by in-situ synthesis from Si/C mixture strongly depends on the nature of the carbon source, which corresponds to the particle size and shape, as well as the preparation temperature. In the experimental conditions, flake graphite is more suitable for the synthesis of SiC powder than activated carbon because of its relatively smaller particle size and flake shape, which make the conversion more complete. The major phase composition of the full conversion products is β-SiC, with traces of α-SiC. Glow discharge mass spectroscopy measurements indicated that SiC powder synthesized with this chemical reaction method can meet the purity demand for the growth of high-resistivity SiC single crystals.
文摘The dielectric properties of nano Si/C/N composite powder and nano SiC powder at high frequencies have been studied. The nano Si/C/N composite powder and nano SiC powder were synthesized from hexamethyldisilazane ((Me 3Si) 2NH) (Me:CH 3) and SiH 4 C 2H 2 respectively by a laser induced gas phase reaction. The complex permittivities of the nano Si/C/N composite powder and nano SiC powder were measured between 8 2GHz and 12 4GHz. The real and imaginary parts of the complex permittivities of nano Si/C/N composite powder are much higher than those of nano SiC powder. The SiC microcrystalline in the nano Si/C/N composite powder dissolved a great deal of nitrogen. The local structure around Si atoms changed by introducing N into SiC. Carbon atoms around Si were substituted by N atoms. So charged defects and quasi free electrons moved in response to the electric field, diffusion or polarization current resulted from the field propagation. The high ε″and loss factor tgδ(ε″/ε′) of Si/C/N composite powder were due to the dielectric relaxation.
基金Funded by National Natural Science Foundation of China(Nos.51502212,51672194 and 51472184)Hubei Province Natural Science Foundation of China(No.2018CFB760)+1 种基金Program for Innovative Teams of Outstanding Young and Middle-aged Researchers in the Higher Education Institutions of Hubei Province(No.T201602)Key Program of Natural Science Foundation of Hubei Province(No.2017CFA004)
文摘Phase pure ZrB2-SiC composite powders were prepared after 1 450℃/3 h via carbothermal reduction route,by using ZrSiO4,B2O3 and carbon as the raw materials.The influences of firing temperature as well as the type and amount of additive on the phase composition of final products were detailedly investigated.The results indicated that the onset formation temperature of ZrB2-SiC was reduced to 1 400℃by the present conditions,and oxide additive（including CoSO4·7H2O,Y2O3 and TiO2）was effective in enhancing the decomposition of raw ZrSiO4,therefore accelerating the synthesis of ZrB2-SiC.Moreover,microstructural observation showed that the as-prepared ZrB2 and SiC respectively had well-defined hexagonal columnar and fibrous morphology.Furthermore,the methodology of back-propagation artificial neural networks（BP-ANNs）was adopted to establish a model for predicting the reaction extent（e g,the content of ZrB2-SiC in final product）in terms of various processing conditions.The results predicted by the as-established BP-ANNs model matched well with that of testing experiment（with a mean square error in 10^（-3） degree）,verifying good effectiveness of the proposed strategy.
基金Project(50572090) supported by the National Natural Science Foundation of China
文摘Nano-SiC powders doped by B were synthesized through the carbothermal reduction of xerogels containing the tributyl borate. The results show that the 3C-SiC with minor phase of 6H-SiC is generated at 1 700 ℃,and that there are not the characteristic peaks of any boride in the XRD patterns,which indicates that the boron is available only on the crystallization of 3C-SiC. The Raman spectra of the samples also show the characteristic bands of 3C-and 6H-SiC at 788 and 965 cm-1. But the bands at 1 345 and 1 590 cm-1 are characteristic peaks of amorphous carbon materials. The intensities of peaks at 788 and 965 cm-1 increase with B content in Raman spectra,which also shift to higher wavenumber with the increasing B. The microstructure of SiC powder is composed of agglomerated particles with diameters ranging from 30 to 100 nm. The results of dielectric property show that the sample with 0.005 B has the largest values in ε′ and ε″ among the four samples due to the existence of the intrinsic defects. But the absence of the relaxation polarization leads to low values of all the samples.
基金Financial support by the National Basic Research Program of China(“973”Program,No.2012CB619600)the National Natural Science Foundation of China(No.51474111)+2 种基金the Science and Technology Development Project of Jilin Province(No.20160519002JH)support came from the Fundamental Research Funds for the Central Universities(JCKY-QKJC02)the Chang Bai Mountain Scholars Program(2013014)
文摘The aging-hardening kinetics of powder metallurgy processed 2014Al alloy and its composite have been studied. The existence of n-SiC particulates leads to the increase of peak hardness. Interestingly, the aginghardening peak of the composite takes place at earlier time than that of the unreinforced alloy. Transmission electron microscopy（TEM） studies indicated that the major precipitation phases are Al_5Cu_2Mn_3 and θ′（Al_2Cu）. Besides, Ω phase appeared in both specimens at peak hardening condition, which has been rarely observed previously in aluminum metal matrix composites without Ag. Accelerated aging kinetics and increased peak hardness may be attributed to the higher dislocation density resulted from the mismatch of coefficients of thermal expansion between n-SiC and 2014Al matrix. The results are beneficial to fabricating high performance composites for the application in automobile field such as pistons, driveshaft tubes, brake rotors, bicycle frames, railroad brakes.
基金supported by grants from the Key Project Fund for Science and Technology Development of Guangdong Province (2020B090924003)the National Natural Science Foundation of China (51975230)Major Special Projects of Technological Innovation in Hubei Province (2019AAA002).
文摘Fabrication of silicon carbide(SiC)ceramics by digital light processing(DLP)technology is difficult owing to high refractive index and high ultraviolet(UV)absorptivity of SiC powders.The surface of the SiC powders can be coated with silicon oxide(SiO_(2))with low refractive index and low UV absorptivity via high-temperature oxidation,reducing the loss of UV energy in the DLP process and realizing the DLP preparation of the SiC ceramics.However,it is necessary to explore a high-temperature modification process to obtain a better modification effect of the SiC powders.Therefore,the high-temperature modification behavior of the SiC powders is thoroughly investigated in this paper.The results show that nano-scale oxide film is formed on the surface of the SiC powders by short-time high-temperature oxidation,effectively reducing the UV absorptivity and the surface refractive index(nʹ)of the SiC powders.When the oxidation temperature is 1300℃,compared with that of unoxidized SiC powders,the UV absorptivity of oxidized SiC powders decreases from 0.5065 to 0.4654,and a curing depth of SiC slurry increases from 22±4 to 59±4μm.Finally,SiC green bodies are successfully prepared by the DLP with the the oxidized powders,and flexural strength of SiC sintered parts reaches 47.9±2.3 MPa after 3 h of atmospheric sintering at 2000℃without any sintering aid.
基金Project(50274021) supported by the National Natural Science Foundation of China and Baoshan Iron and Steel Co. Ltd.
文摘ZrO2-SiC composite powder was synthesized by carbothermal reduction of zircon in argon atmosphere, and it was used as the additive to prepare Al2O3-C refractories. The effects of heating temperature on the synthesis process and the addition of the synthesized composite powder on the properties of the Al2O3-C refractories were investigated. The results show that the synthesized composite powder can be easily obtained by heating the mixture of zircon and carbon black at 1 873 K for 4 h in argon atmosphere, and the relative contents of ZrO2 and SiC in sample reach about 83.7% and 16.3%, respectively. The bulk density, crushing strength and thermal shock resistance of the Al2O3-C refractories can be improved obviously by the addition of the synthesized ZrO2-SiC composite powder.
基金Project (50572090) supported by the National Natural Science Foundation of China
文摘SiC-Al2O3 composite powder was prepared by sol-gel and carbothermal reduction method. The powder synthesized was characterized by X-ray diffraction(XRD) and scanning electron microscopy(SEM) to confirm the phase formation, and the thermodynamic analysis was performed systematically. Moreover, the variation of its microwave permittivity with different atomic ratio of Al/Si was investigated in the frequency range of 8.2-12.4 GHz. The results show that, the powder obtained consists of spherical particles of 300-400 nm in diameter, which are composed of SiC and Al2O3 microcrystal with the grain size of approximately 45 nm. The results of XRD accord with those of the thermodynamic analysis. It is impossible for Al atoms to dissolve in the lattice of SiC during the carbothermal reduction process. Along with the increase of atomic ratio of Al/Si in the xerogel, the amount of Al2O3 in the powder synthesized increases, which reduces bothε', the real part of complex permittivity, and tgδ(ε'/ε'), the dissipation factor, whereε' is the imaginary part of complex permittivity.
文摘The properties of SiC kiln furniture bonded with fine silicon powderare related to the bonder’s crystal structure. At high temperature, it will crystallize ina-cristobalite with great bulk effect. MnO2 mineralizer can make a-cristobalite convertto a-tridymite whose bulk effect is small. The crystal structure and its amount were investigated with XRD technique. The influence of different amounts of MnO2 on thecrystal structure and polycrystal transformation, and that of crystal structure on theproperties of kiln furniture were studied. The best proportion of MnO2 added was determined to be 2.0%.
基金This work was financially supported by the Science Fund for Distinguished Young Scholars of Henan Province, China (No. 0512002400)
文摘Co-SiC core-shell powders were prepared by electroless plating. Scanning electron microscopy （SEM） revealed that Co-SiC core-shell powders were of nearly sphere-like shape and were about 0.3 pan. X-ray powder diffraction （XRD） patterns showed that the cobalt powder was hexagonal crystallite. The complex dielectric constant and the complex permeability of Co-SiC core-shell powders-paraffin wax composite were measured by the rectangle wavegnide method. It showed that the dielectric loss was less than 0.1 and the magnetic loss was about 0.2 in 8.2-12.4 GHz for prepared Co-SiC core-shell comoosite oowders.
文摘Nickel oxide (NiO) powder is prepared by decomposition of basic nickel carbonate (mNiCO3.nNi(OH)2.xH2O) (BNC) in microwave field with silicon carbide (SiC) as an indirect heating medium. The decomposition proceeds stage by stage: firstly BNC removes its crystal water with the heat provided by BNC itself and SiC which absorb microwave energy,then removes CO2 and H2O from the anhydride (mNiCO3 .nNi(OH)2) and begins to produce NiO with the heat provided by SiC, and finally decomposes into NiO powder completely with the heat provided by the produced NiO which absorbs microwave energy strongly. In the microwave irradiation process, the decomposition of BNC can be accelerated by increasing the amount of BNC, the amount of SiC and the microwave field power. The size of the NiO granule is about 18ourn when the size of BNC used is about 15ourn.
基金Funded by the Research Collaborative Innovation Project of Jiangsu Province,China(BY2009129)the Science and Technology Project of Suzhou,China(SYG0905)
文摘β-SiC nanoparticle reinforced A1 matrix （nano-SiCp/A1） composite was prepared by a multi- step powder metallurgy strategy including presureless sintering, hot compacting process and hot extrusion. The microstructures of the as-prepared composites were observed by scanning electronic microscopy （SEM）, and the mechanical properties were characterized by tensile strength measurement and Brinell hardness test. The experimental results revealed that the tensile strength of the composite with the addition of 5wt%/3-SIC nanoprtieles could be increased to 215 MPa, increasing by 110% compared with pure A1 matrix. Comparative experiments reflected that theβ-SIC nanoprticles showed significant reinforcement effect than traditional a-SiC micro-sized particles. The preparation process and sintering procedure were investigated to develop a cost effective preparation strategy to fabricate nano-SiCp/A1 composite.
基金Project supported by the National Natural Science Foundation of China (50672060 and 50372041)Projectof Liaoning Province Government (20052002)
文摘Low cost silicon carbon nanometer powder was synthesized by carbothermal reduction method with nanometer SiO2 and carbon as raw material. Its synthesis thermodynamics were discussed. The influence of La on TG-DSC curve was also analyzed. It indicated that the synthesis process of SiC powder had two steps. In the first step two medial productions of SiOg and COg formed, and in the second step, β-SiC was finally synthesized. After 0.3% La added, at the first step, the initiatory forming temperature of producing SiO(g) and CO(g) declined from 1351.4 to 1250.9 ℃, and the thermal activation energy decreased from 223.6 to 34.7 J·g-1; at the second step the initiatory forming temperature of synthesizing β-SiC powder declined from 1526.5 to 1357.8 ℃, and the thermal activation energy decreased from 693.7 to 295.7 J·g-1. Without La added, the best synthesis technology for β-SiC powder was 1550 ℃ for 120 min, average powder diameter was bigger about 150 nm. With La added, the best synthesis technology was 1500 ℃ for 120 min, average powder diameter was about 100 nm.
