Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0....Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0.12)O_(2)mixed oxides was realized via a facile and scalable approach,namely,sulfateaided coprecipitation method was labelled as CZ-S.Sulfate ion(SO_(4)^(2-))was added into raw solution in the form of sulfuric acid and acted as coordination agent.The control sample was prepared by conventional coprecipitation method without sulfuric acid added and labelled as CZ.The promotion effect of sulfate ion was analyzed systematically by X-ray diffraction(XRD),transmission electron microscopy(TEM),scanning electron microscopy(SEM),N_(2)adsorption-desorption,Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),OSC and hydrogen temperatureprogrammed reduction(H_(2)-TPR)analysis.XRD and high resolution TEM results reveal that CZ-S have homogeneous distributions of elements.TEM and SEM images show that fresh samples of CZ-S have narrower distributions of grain sizes and larger pore sizes than those of CZ.Through cross analysis of structure and morphology of CZ and CZ-S,we find that the introduction of sulfate ions results in uniform distributions of elements,narrows distributions of grain sizes,and enables the formation of secondary loose packing of sub-particles,which lead to enhanced thermal stability of the samples of CZ-S upon aging process at high temperature.After aging treatment at 1100℃for 10 h,aged samples of CZ-S present larger specific surface areas and pore volumes than the aged sample prepared by conventional coprecipitation method without sulfate ions added.Furthermore,the aged sample of CZ-S2(SO_(4)^(2-)/Zr=1)possesses the highest specific surface area of 21.9 m2/g and the biggest pore volume of 0.035 mL/g among all aged samples.展开更多
The electrocatalysts of Pt/C, PtRu/C and Ru/C were prepared by the impregnation method. The facet characterization, the dispersion and the particle size for the catalysts were determined by means of X ray diffractio...The electrocatalysts of Pt/C, PtRu/C and Ru/C were prepared by the impregnation method. The facet characterization, the dispersion and the particle size for the catalysts were determined by means of X ray diffraction and transmission electron microscopy. X ray photoelectron spectroscopy was also used to analyze the state and the valency of the noble metals. The results show that the particle size was in nanometer range and the binary metals have come into being an alloy. The platinum in the catalysts existed in zero valency. The valency of the ruthenium on the surface is different from that in the body, while the ruthenium on the surface existed in oxide form. PtRu/C and Pt/C are of good activity to the electrooxidation of hydrogen except Ru/C. PtRu/C is more tolerant of CO than Pt/C, and CO is only adsorbed on Pt.展开更多
Nanocrystalline Ni0.5Zn0.5 ferrite with average grain sizes ranging from 10 to 100 nm is prepared by using a spraying-coprecipitation method. The results indicate that the nanocrystalline Ni0.5Zn0.5 ferrite is ferroma...Nanocrystalline Ni0.5Zn0.5 ferrite with average grain sizes ranging from 10 to 100 nm is prepared by using a spraying-coprecipitation method. The results indicate that the nanocrystalline Ni0.5Zn0.5 ferrite is ferromagnetic without the superparamagnetic phenomenon observed at room temperature. Specific saturation magnetization of nanocrystalline Nio.sZno.5 ferrite increases from 40.2 to 75.6 emu/g as grain size increases from 11 to 94nm. Coercivity of nanocrystalline Ni0.5Zn0.5 ferrite increases monotonically when d 〈 62 nm.The relationship between the coercivity and the mean grain size is well fitted into a relation Hc - d^3. A theoretically evaluated value of the critical grain size is 141nm larger than the experimental value 62nm for nanocrystalline Ni0.5Zn0.5 ferrite. The magnetic behaviour of nanocrystalline Ni0.5Zn0.5 ferrite may be explained by using the random anisotropy theory.展开更多
With zirconium oxychloride, nitrate of lime and ammonia as raw materials, nano powder of CaO ZrO 2 was prepared by chemical coprecipitation method. By use of azeotropic distillation processing, chemical coprecipitatio...With zirconium oxychloride, nitrate of lime and ammonia as raw materials, nano powder of CaO ZrO 2 was prepared by chemical coprecipitation method. By use of azeotropic distillation processing, chemical coprecipitation precursor was obtained. Phase transformation of the precursor was observed at the temperature of 593.81 ℃ and 1 234.56 ℃ respectively with DTA analyses. Phase structure was analyzed through XRD and Raman spectra. The average particle size of tetragonal zirconium oxide powder was 9.8 and 43.7 nm after calcination at 600 and 1 100 ℃ respectively which was tested by TEM and BET analyses. Furthermore, the influences of the doping of nitrate of lime and the average particle size of zirconium oxide on the stability of tetragonal zirconium oxide were also discussed.展开更多
Nanocrystalline Ni1-xZnxFe2O4 ferrites with 0≤x≤1 were successfully prepared by a spraying-coprecipitation method.The microstructure was investigated by using XRD and TEM.Magnetic properties were measured with vibra...Nanocrystalline Ni1-xZnxFe2O4 ferrites with 0≤x≤1 were successfully prepared by a spraying-coprecipitation method.The microstructure was investigated by using XRD and TEM.Magnetic properties were measured with vibrating sample magnetometer（VSM） at room temperature.The results show that the grain size of nanocrystalline Ni1-xZnxFe2O4 ferrite calcined at 600 ℃ for 1.5 h is about 30 nm.Lattice parameter and specific saturation magnetization Ms of nanocrystalline Ni1-xZnxFe2O4 ferrite increase with the Zn^2＋ ions content at room temperature,and maximum Ms is 66.8 A·m^2·kg^-1 as the Zn^2＋ ions content is around 0.5,and coercivity Hc of the nanocrystalline Ni1-xZnxFe2O4 ferrite decreases with Zn^2＋ ions content.展开更多
LiNi0.5Mn1.5O4 was synthesized by two different coprecipitation methods:composite carbonate process and composite hydroxide method. The effects of calcination temperature of precursors on the physical properties and e...LiNi0.5Mn1.5O4 was synthesized by two different coprecipitation methods:composite carbonate process and composite hydroxide method. The effects of calcination temperature of precursors on the physical properties and electrochemical performance of the samples were investigated. The results of scanning electron microscopy(SEM) show that as calcination temperature increases,the crystallinity of the samples is improved,and their grain sizes are obviously increased. X-Ray diffraction(XRD) data show that the LiNi0.5Mn1.5O4 compounds obtained by two coprecipitation methods both exhibit a pure cubic spinel structure without any impurities. Furthermore,it is found that the samples prepared with relatively high temperature precursors present large initial discharge capacity(>125 mA·h/g) and excellent cycling stability with a capacity retention rate larger than 91% after 30 cycles at current density of 1 C. This probably derives from their higher crystallinity and larger grain sizes. However,the initial discharge capacity of LiNi0.5Mn1.5O4 synthesized by composite carbonate process is smaller than that prepared by composite carbonate process,but it shows better capacity retention ability.展开更多
The α-SiC in 0.5μm size powders were coated with Al_2O_3 and Y_2O_3 by a coprecipitation coating (CPC) method forfabrication of SiC/YAG composites. The same powder preparation was carried out by conventional mechani...The α-SiC in 0.5μm size powders were coated with Al_2O_3 and Y_2O_3 by a coprecipitation coating (CPC) method forfabrication of SiC/YAG composites. The same powder preparation was carried out by conventional mechanical mixing(MM) method for comparison. Two kinds of SiC/YAG composites were manufactured by pressureless sintering usingthe different powders, named CPC composite and MM composite thereafter respectively. It is shown that the CPCcomposite has the advantages of homogeneous distribution of YAG phase and of being sintered to high density ata low temperature, 100℃ lower than that of MM composite. The strength (573 MPa) and hardness (23.3 GPa) ofthe CPC composite are significantly higher than those (323 MPa and 13.5 GPa) of the MM composite, respectively.展开更多
The objective of this work is to study the synthesis of copper-alumina nanocomposites using the coprecipitation process and hot-pressing method, and investigate their mechanical properties. The effects of calcination ...The objective of this work is to study the synthesis of copper-alumina nanocomposites using the coprecipitation process and hot-pressing method, and investigate their mechanical properties. The effects of calcination temperature on the average size of composite particles and chemical composition after calcination were also analyzed. The sintering parameters including sintering temperature, hot pressure and packing time were optimized to fabricate the alumina nanoparticles reinforced copper matrix composites（CMCs）. The density, microhardness and tribological properties of the CMCs reinforced with 1 wt%, 2 wt%, 3 wt%, 4 wt% and 5 wt% of alumina nanoparticles were investigated correspondingly. The results showed that the optimum preparation parameters for the CMCs were 900 ℃ of hot pressing temperature, 27.5 MPa of hot pressure and 2 hrs of packing time. The CMC reinforced with 2 wt% of alumina nanoparticles had the lowest wear rate, with the relative wear resistance of 3.13.展开更多
Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal ...Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal indium in HNO3.The tin solution was obtained by dissolving metal tin in HNO3 and followed by stabilizing with citric acid.The free of chlorine ions in the synthesis process brought several advantages：shortening the synthesis time,decreasing the particle agglomeration,decreasing the chlorine content in the ITO nanoparticles and improving the particle sinterability.This is the first time to report the synthesis of ITO nanoparticles free from chlorine contamination without using the expensive metal alkoxides as starting materials.展开更多
CoFe2O4 nanoparticles （NPs） were synthesized by coprecipitation method using FeCl3·6H2O and CoCl2·6H2O as precursors.The synthesized conditions were optimized,such as added means of precipitator,quantity o...CoFe2O4 nanoparticles （NPs） were synthesized by coprecipitation method using FeCl3·6H2O and CoCl2·6H2O as precursors.The synthesized conditions were optimized,such as added means of precipitator,quantity of precipitator,the mol ratio of Fe 3＋ to Co2＋,reaction temperature and pH value.The synthesized material was characterized by XRD,TEM,FTIR,EDS,Raman and its magnetic properties were studied by VSM.The experimental results confirm that the sample is cubic spinel structure CoFe2O4 with a narrow size distribution and a good dispersion feature.CoFe2O4 NPs with well-controlled shape and size was obtained at 70℃.The magnetic properties indicate superparamagnetic behavior and good saturated magnetization.展开更多
The addition of the second phase into tungsten can significantly refine the grain size of tungsten alloys,and also play a role in dispersion strengthening,thus improving the properties of tungsten alloy.As a preparati...The addition of the second phase into tungsten can significantly refine the grain size of tungsten alloys,and also play a role in dispersion strengthening,thus improving the properties of tungsten alloy.As a preparation method of tungsten alloy powder,liquid-phase method avoids the disadvantage of mechanical alloying,and the obtained powder composition is accurate and controllable,with high purity and excellent uniformity.At present,the second phase particles used for dispersion strengthening tungsten alloys are mainly composed of oxides.Oxide particles can be synthesized and precipitated in nitrate solution through in situ chemical reaction,and are uniformly distributed in composite powder by mixing and stirring.Finally,the oxide dispersion strengthened tungsten alloy(ODS-W)was obtained by reduction and sintering.Liquid-phase methods for preparing ODS-W alloys include azeotropic distillation,sol-gel methods,freeze-drying,hydrothermal synthesis,spray-drying,etc.In this paper,several liquid-phase methods for preparing tungsten alloy composite powder precursors are reviewed,and their latest research progresses are discussed.In addition,the morphologies and properties of tungsten alloys prepared by different methods are compared,which provides guidance for preparing high-performance tungsten alloys.展开更多
Mgo-Cao refractories are widely used in the iron and steel metalurgy industry due to their advantages of purifying molten steel,high refractoriness,good thermal shock resistance,and excellent corrosion resistance to b...Mgo-Cao refractories are widely used in the iron and steel metalurgy industry due to their advantages of purifying molten steel,high refractoriness,good thermal shock resistance,and excellent corrosion resistance to basic slags.However,hydration occurs during the manufacturing,storage,and transportation of refractories,which severely limits their application.Mgo-CaO clinker is the main raw material for Mgo-Cao refractories,and its hydration resistance determines the development of the latter case.Herein,the Mgo-Cao clinker was modified using myristic acid as the modifying agent by the liquid-phase deposition method.The effects of the particle size of the raw materials,concentration of myristic acid,treatment temperature and time on the phase composition and hydration resistance of the modified Mgo-Cao clinkers were investigated in detail.The results show that the samples with an agent concentration of 0.25 mol L^(-1) and treated at 25℃ for 1 h exhibit the optimal hydration resistance properties,namely a low hydration mass gain rate(0.23%)and a large water contact angle(152.9).展开更多
基金Project supported by Beijing Nova Program(Z181100006218030)。
文摘Ceria-zirconia based mixed oxides(CZs)have been applied in three-way catalysts(TWCs)for their high surface area and oxygen storage capacity(OSC).In this work,enhanced thermal stability of Ce_(0.33)Zr_(0.55)(LaNdY)_(0.12)O_(2)mixed oxides was realized via a facile and scalable approach,namely,sulfateaided coprecipitation method was labelled as CZ-S.Sulfate ion(SO_(4)^(2-))was added into raw solution in the form of sulfuric acid and acted as coordination agent.The control sample was prepared by conventional coprecipitation method without sulfuric acid added and labelled as CZ.The promotion effect of sulfate ion was analyzed systematically by X-ray diffraction(XRD),transmission electron microscopy(TEM),scanning electron microscopy(SEM),N_(2)adsorption-desorption,Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),OSC and hydrogen temperatureprogrammed reduction(H_(2)-TPR)analysis.XRD and high resolution TEM results reveal that CZ-S have homogeneous distributions of elements.TEM and SEM images show that fresh samples of CZ-S have narrower distributions of grain sizes and larger pore sizes than those of CZ.Through cross analysis of structure and morphology of CZ and CZ-S,we find that the introduction of sulfate ions results in uniform distributions of elements,narrows distributions of grain sizes,and enables the formation of secondary loose packing of sub-particles,which lead to enhanced thermal stability of the samples of CZ-S upon aging process at high temperature.After aging treatment at 1100℃for 10 h,aged samples of CZ-S present larger specific surface areas and pore volumes than the aged sample prepared by conventional coprecipitation method without sulfate ions added.Furthermore,the aged sample of CZ-S2(SO_(4)^(2-)/Zr=1)possesses the highest specific surface area of 21.9 m2/g and the biggest pore volume of 0.035 mL/g among all aged samples.
基金Supported by the National 973project(No.G2 0 0 0 0 2 6 4 10 ) and Inovation Funds of Dalian Insitute of Chem icalPhysics
文摘The electrocatalysts of Pt/C, PtRu/C and Ru/C were prepared by the impregnation method. The facet characterization, the dispersion and the particle size for the catalysts were determined by means of X ray diffraction and transmission electron microscopy. X ray photoelectron spectroscopy was also used to analyze the state and the valency of the noble metals. The results show that the particle size was in nanometer range and the binary metals have come into being an alloy. The platinum in the catalysts existed in zero valency. The valency of the ruthenium on the surface is different from that in the body, while the ruthenium on the surface existed in oxide form. PtRu/C and Pt/C are of good activity to the electrooxidation of hydrogen except Ru/C. PtRu/C is more tolerant of CO than Pt/C, and CO is only adsorbed on Pt.
文摘Nanocrystalline Ni0.5Zn0.5 ferrite with average grain sizes ranging from 10 to 100 nm is prepared by using a spraying-coprecipitation method. The results indicate that the nanocrystalline Ni0.5Zn0.5 ferrite is ferromagnetic without the superparamagnetic phenomenon observed at room temperature. Specific saturation magnetization of nanocrystalline Nio.sZno.5 ferrite increases from 40.2 to 75.6 emu/g as grain size increases from 11 to 94nm. Coercivity of nanocrystalline Ni0.5Zn0.5 ferrite increases monotonically when d 〈 62 nm.The relationship between the coercivity and the mean grain size is well fitted into a relation Hc - d^3. A theoretically evaluated value of the critical grain size is 141nm larger than the experimental value 62nm for nanocrystalline Ni0.5Zn0.5 ferrite. The magnetic behaviour of nanocrystalline Ni0.5Zn0.5 ferrite may be explained by using the random anisotropy theory.
文摘With zirconium oxychloride, nitrate of lime and ammonia as raw materials, nano powder of CaO ZrO 2 was prepared by chemical coprecipitation method. By use of azeotropic distillation processing, chemical coprecipitation precursor was obtained. Phase transformation of the precursor was observed at the temperature of 593.81 ℃ and 1 234.56 ℃ respectively with DTA analyses. Phase structure was analyzed through XRD and Raman spectra. The average particle size of tetragonal zirconium oxide powder was 9.8 and 43.7 nm after calcination at 600 and 1 100 ℃ respectively which was tested by TEM and BET analyses. Furthermore, the influences of the doping of nitrate of lime and the average particle size of zirconium oxide on the stability of tetragonal zirconium oxide were also discussed.
基金Funded by the Natural Science Foundation of High Education School ofAnhui Province,China (Nos:KJ2007B0271 and KJ2010A095)
文摘Nanocrystalline Ni1-xZnxFe2O4 ferrites with 0≤x≤1 were successfully prepared by a spraying-coprecipitation method.The microstructure was investigated by using XRD and TEM.Magnetic properties were measured with vibrating sample magnetometer（VSM） at room temperature.The results show that the grain size of nanocrystalline Ni1-xZnxFe2O4 ferrite calcined at 600 ℃ for 1.5 h is about 30 nm.Lattice parameter and specific saturation magnetization Ms of nanocrystalline Ni1-xZnxFe2O4 ferrite increase with the Zn^2＋ ions content at room temperature,and maximum Ms is 66.8 A·m^2·kg^-1 as the Zn^2＋ ions content is around 0.5,and coercivity Hc of the nanocrystalline Ni1-xZnxFe2O4 ferrite decreases with Zn^2＋ ions content.
基金Project(2007CB613607) supported by the National Basic Research Program of China
文摘LiNi0.5Mn1.5O4 was synthesized by two different coprecipitation methods:composite carbonate process and composite hydroxide method. The effects of calcination temperature of precursors on the physical properties and electrochemical performance of the samples were investigated. The results of scanning electron microscopy(SEM) show that as calcination temperature increases,the crystallinity of the samples is improved,and their grain sizes are obviously increased. X-Ray diffraction(XRD) data show that the LiNi0.5Mn1.5O4 compounds obtained by two coprecipitation methods both exhibit a pure cubic spinel structure without any impurities. Furthermore,it is found that the samples prepared with relatively high temperature precursors present large initial discharge capacity(>125 mA·h/g) and excellent cycling stability with a capacity retention rate larger than 91% after 30 cycles at current density of 1 C. This probably derives from their higher crystallinity and larger grain sizes. However,the initial discharge capacity of LiNi0.5Mn1.5O4 synthesized by composite carbonate process is smaller than that prepared by composite carbonate process,but it shows better capacity retention ability.
基金This work was supported by the National Natural Science Foundation of China(No.50372041)National“863”Plan(No.2003AA305620).
文摘The α-SiC in 0.5μm size powders were coated with Al_2O_3 and Y_2O_3 by a coprecipitation coating (CPC) method forfabrication of SiC/YAG composites. The same powder preparation was carried out by conventional mechanical mixing(MM) method for comparison. Two kinds of SiC/YAG composites were manufactured by pressureless sintering usingthe different powders, named CPC composite and MM composite thereafter respectively. It is shown that the CPCcomposite has the advantages of homogeneous distribution of YAG phase and of being sintered to high density ata low temperature, 100℃ lower than that of MM composite. The strength (573 MPa) and hardness (23.3 GPa) ofthe CPC composite are significantly higher than those (323 MPa and 13.5 GPa) of the MM composite, respectively.
基金Funded by Jiangsu Innovation Program for Graduate EducationFundamental Research Funds for the Central Universities(No.KYLX_0258)+1 种基金Opening Project of Jiangsu Key Laboratory of Advanced Structural Materials and Application Technology(No.ASMA201401)Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘The objective of this work is to study the synthesis of copper-alumina nanocomposites using the coprecipitation process and hot-pressing method, and investigate their mechanical properties. The effects of calcination temperature on the average size of composite particles and chemical composition after calcination were also analyzed. The sintering parameters including sintering temperature, hot pressure and packing time were optimized to fabricate the alumina nanoparticles reinforced copper matrix composites（CMCs）. The density, microhardness and tribological properties of the CMCs reinforced with 1 wt%, 2 wt%, 3 wt%, 4 wt% and 5 wt% of alumina nanoparticles were investigated correspondingly. The results showed that the optimum preparation parameters for the CMCs were 900 ℃ of hot pressing temperature, 27.5 MPa of hot pressure and 2 hrs of packing time. The CMC reinforced with 2 wt% of alumina nanoparticles had the lowest wear rate, with the relative wear resistance of 3.13.
基金supported by the Ph.D. programs Foundation of Ministry of Education of China (No.200802511022)
文摘Indium tin oxide （ITO） nanoparticles with crystallite size of 12.6 nm and specific surface area of 45.7 m 2 ·g-1 were synthesized by co-precipitation method.The indium solution was obtained by dissolving metal indium in HNO3.The tin solution was obtained by dissolving metal tin in HNO3 and followed by stabilizing with citric acid.The free of chlorine ions in the synthesis process brought several advantages：shortening the synthesis time,decreasing the particle agglomeration,decreasing the chlorine content in the ITO nanoparticles and improving the particle sinterability.This is the first time to report the synthesis of ITO nanoparticles free from chlorine contamination without using the expensive metal alkoxides as starting materials.
基金Funded by the National Natural Science Foundation of China(No.60877048)
文摘CoFe2O4 nanoparticles （NPs） were synthesized by coprecipitation method using FeCl3·6H2O and CoCl2·6H2O as precursors.The synthesized conditions were optimized,such as added means of precipitator,quantity of precipitator,the mol ratio of Fe 3＋ to Co2＋,reaction temperature and pH value.The synthesized material was characterized by XRD,TEM,FTIR,EDS,Raman and its magnetic properties were studied by VSM.The experimental results confirm that the sample is cubic spinel structure CoFe2O4 with a narrow size distribution and a good dispersion feature.CoFe2O4 NPs with well-controlled shape and size was obtained at 70℃.The magnetic properties indicate superparamagnetic behavior and good saturated magnetization.
基金supported by National Natural Science Foundation of China(no.U2004180)。
文摘The addition of the second phase into tungsten can significantly refine the grain size of tungsten alloys,and also play a role in dispersion strengthening,thus improving the properties of tungsten alloy.As a preparation method of tungsten alloy powder,liquid-phase method avoids the disadvantage of mechanical alloying,and the obtained powder composition is accurate and controllable,with high purity and excellent uniformity.At present,the second phase particles used for dispersion strengthening tungsten alloys are mainly composed of oxides.Oxide particles can be synthesized and precipitated in nitrate solution through in situ chemical reaction,and are uniformly distributed in composite powder by mixing and stirring.Finally,the oxide dispersion strengthened tungsten alloy(ODS-W)was obtained by reduction and sintering.Liquid-phase methods for preparing ODS-W alloys include azeotropic distillation,sol-gel methods,freeze-drying,hydrothermal synthesis,spray-drying,etc.In this paper,several liquid-phase methods for preparing tungsten alloy composite powder precursors are reviewed,and their latest research progresses are discussed.In addition,the morphologies and properties of tungsten alloys prepared by different methods are compared,which provides guidance for preparing high-performance tungsten alloys.
基金National Natural Science Foundation of China(Grants 52202025 and U23A20559)Natural Science Foundation of Hubei Province(Grant 2022CFB629)+1 种基金"The 14^(th)Five-Year Plan"Hubei Provincial Advantaged Characteristic Disciplines(Groups)Project of Wuhan University of Science and Technology(2023A0307).
文摘Mgo-Cao refractories are widely used in the iron and steel metalurgy industry due to their advantages of purifying molten steel,high refractoriness,good thermal shock resistance,and excellent corrosion resistance to basic slags.However,hydration occurs during the manufacturing,storage,and transportation of refractories,which severely limits their application.Mgo-CaO clinker is the main raw material for Mgo-Cao refractories,and its hydration resistance determines the development of the latter case.Herein,the Mgo-Cao clinker was modified using myristic acid as the modifying agent by the liquid-phase deposition method.The effects of the particle size of the raw materials,concentration of myristic acid,treatment temperature and time on the phase composition and hydration resistance of the modified Mgo-Cao clinkers were investigated in detail.The results show that the samples with an agent concentration of 0.25 mol L^(-1) and treated at 25℃ for 1 h exhibit the optimal hydration resistance properties,namely a low hydration mass gain rate(0.23%)and a large water contact angle(152.9).
