Y 2O 3 nanoparticles organosol coated with DBS was prepared by microemulsion method. The optimum preparative conditions of Y 2O 3 nanoparticles organosol were obtained. TEM analysis indicates that the prepared Y ...Y 2O 3 nanoparticles organosol coated with DBS was prepared by microemulsion method. The optimum preparative conditions of Y 2O 3 nanoparticles organosol were obtained. TEM analysis indicates that the prepared Y 2O 3 nanoparticles are spherical in shape. The size is about 5 nm. The size distribution is in the narrow range and no agglomerates are observed. Y 2O 3 nanoparticles coated with DBS are easy to dissolve in weak polar solvents.展开更多
Long afterglow phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） were synthesized by microemulsion method, and their crystal structure and luminescent properties were compared and investigated. XRD patterns of samp...Long afterglow phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） were synthesized by microemulsion method, and their crystal structure and luminescent properties were compared and investigated. XRD patterns of samples indicate that phosphors CaAl2O4：Eu^2＋, Dy^3＋ and SrAl2O4 ： Eu^2＋, Dy^3＋ are with monoelinie crystal structure and phosphor BaAl2O4：Eu^2＋ , Dy^3＋ is with hexagonal crystal structure. The wide range of excitation spectrum of phosphors MAl2O4： Eu^2 ＋ , Dy^3＋ （M = Ca,Sr, Ba） indicates that the luminescent materials can he excited by light from ultraviolet ray to visible light and the maximum emission wavelength of phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） is found mainly at λem of 440 nm （M = Ca）, 520 nm （M = Sr） and 496 nm （M = Ba） respectively, the corresponding colors of emission light are blue, green and eyna-green respectively. The afterglow decay tendency of phosphors can he summarized as three processes： initial rapid decay, intermediate transitional decay and very long slow decay. Afterglow decay curves coincide with formula I = At^ - n, and the sequence of afterglow intensity and time is Sr 〉 Ca 〉 Ba.展开更多
A microemulsion-mediated hydrothermal method for synthesis of YVO4:RE(RE=Yb 3+/Er 3+,Yb 3+/Tm 3+)nanoparticles by hydrothermal treatment of quaternary microemulsion medium consisting of Na3VO4/NaOH and RE(NO3)3 aqueou...A microemulsion-mediated hydrothermal method for synthesis of YVO4:RE(RE=Yb 3+/Er 3+,Yb 3+/Tm 3+)nanoparticles by hydrothermal treatment of quaternary microemulsion medium consisting of Na3VO4/NaOH and RE(NO3)3 aqueous solution, surfactant cetyltrimethylammonium bromide(CTAB),cosurfactant n-hexanol and oil phase n-heptane was report.The confinement of microemulsion droplets acting as microreactors during the reaction process allows the formation of small size YVO4:RE nanoparticles with relatively narrow size distribution and less aggregation.The structure,size and shape of YVO4:RE nanoparticles were investigated by means of X-ray diffractometry(XRD)and transmission electron microscopy(TEM).Compared with the conventional solid annealing diffusion method,the microemulsion-mediated hydrothermal method shows superiority in obtaining YVO4:RE nanoparticles with controllable size,narrow size distribution and less aggregation.The microemulsion-mediated hydrothermal method may be potentially applicable for synthesis of other rare earth doped up-converting luminescence nanomaterials.展开更多
Polysiloxane latexes were prepared by microemulsion polymerization of octamethylcyclotetrasiloxane （D4） in the absence of co-emulsifier with octadecyl trimethyl ammonium chloride as a cationic emulsifier and potassi...Polysiloxane latexes were prepared by microemulsion polymerization of octamethylcyclotetrasiloxane （D4） in the absence of co-emulsifier with octadecyl trimethyl ammonium chloride as a cationic emulsifier and potassium hydrate as an initiator. The particle size was determined by the dynamic light scattering （DLS） technique and the reaction rates of the polymerization were discussed. Furthermore, the kinetics was studied by an initial-rate method, and the effects of the monomer, emulsifier and initiator concentrations and the temperature on polymerization conversions were investigated. From the kinetic results, the rate of polymerization, Rp at 80℃ can be expressed as Rp = k[D4]^0.79 [OTAC]^0.64[KOH]^0.38 and the aonarent activation energy（Ea）. which was determined by half-period method, is 95.32 kJ mol^-1.展开更多
Nanocrystalline TiO2 powders with high photocatalytic activity were prepared by one-step microemulsion-mediated hydrothermal method using tetrabutylorthotitanate (TiO(C4H9)4, TBOT) as precursor. The as-prepared TiO2 p...Nanocrystalline TiO2 powders with high photocatalytic activity were prepared by one-step microemulsion-mediated hydrothermal method using tetrabutylorthotitanate (TiO(C4H9)4, TBOT) as precursor. The as-prepared TiO2 powders were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and the Brunauer-Emmett-Teller (BET) specific surface area measurements. The effects of the oil/water ratio and hydrothermal temperature on the microstructures and photocatalytic activity of the TiO2 powders were investigated. The results suggest that increasing the oil/water emulsion ratio significantly decreased the particle size of the as-prepared TiO2 powders and improved the photocatalytic activity. With hydrothermal temperature increasing, the average crystallite size increased and the photocatalytic activities of TiO2 powders decreased.展开更多
The CeO_2-ZrO_2 solid solutions were prepared by a reverse microemulsion method. The effect of preparation parameters on the surface area and crystalline form of the solid solutions were studied by the BET surface are...The CeO_2-ZrO_2 solid solutions were prepared by a reverse microemulsion method. The effect of preparation parameters on the surface area and crystalline form of the solid solutions were studied by the BET surface area and XRD analysis. The studies indicate that the separation of the microemulsion phase during the preparation procedure can decrease the specific surface area of sample, adding hydrogen peroxide in the matrix solution can increase the specific surface area and stability of sample. The surface area of sample calcined at 550 ℃ for 5 h is 149 m^2·g^(-1), and that calcined at 900 ℃ for 6 h is 88 m^2·g^(-1). The sample with tetragonal symmetry Ce_(0.5)Zr_(0.5)O_2 phase has a higher stability.展开更多
In this study, the CaP/pDNA nanoparticles were prepared using Triton X-100/Butanol/Cyclohexane/Water reverse microemulsion system. Optimization of preparation conditions was based on evaluation of particle size by Box...In this study, the CaP/pDNA nanoparticles were prepared using Triton X-100/Butanol/Cyclohexane/Water reverse microemulsion system. Optimization of preparation conditions was based on evaluation of particle size by Box–Behnken design method. The particle sizes of the optimized CaP/pDNA nanoparticles were found to be 60.23 ± 4.72 nm, polydispersity index was 0.252 and pDNA encapsulate efficiency was more than 90%. The optimized CaP/pDNA nanoparticles have pH sensitivity and biocompatibility. Further, optimized CaP/pDNA nanoparticles showed higher transfection efficiency.展开更多
Adsorption isotherm is the most fundamental information related to chromatography. To calculate the parameters of Langmuir ad-sorption isotherm of thymidine, frontal analysis (FA) and elution-curve method (ECM) were a...Adsorption isotherm is the most fundamental information related to chromatography. To calculate the parameters of Langmuir ad-sorption isotherm of thymidine, frontal analysis (FA) and elution-curve method (ECM) were adopted in reversed-phase high performance liguid chromatography (RP-HPLC). In FA, the concentration of stationary phase was measured from the elution curves and the isotherm was deter-mined by regression analysis, while the parameters by ECM were obtained by parameter optimization. The adsorption isotherms of thymidine from the two methods were very similar. The superiority of ECM over FA was that the consumption of sample was less and only one or two in-jections of sample were required.展开更多
A new microemulsion method using tetraoctylammonium bromide as a cationic surfactant has been formulated to fabricate thiol-functionalized gold nanoparticles, The nanoparticles were compared with those synthesized by ...A new microemulsion method using tetraoctylammonium bromide as a cationic surfactant has been formulated to fabricate thiol-functionalized gold nanoparticles, The nanoparticles were compared with those synthesized by the multistep Brust two-phase method.The nanoparticle sizes and size distributions fabricated by the two methods were characterized by UV-vis ahsorbance spectroscopy and transmittance electron microscopy. The simple microemulsion method produced the same results as those obtained by the Brust method,展开更多
文摘Y 2O 3 nanoparticles organosol coated with DBS was prepared by microemulsion method. The optimum preparative conditions of Y 2O 3 nanoparticles organosol were obtained. TEM analysis indicates that the prepared Y 2O 3 nanoparticles are spherical in shape. The size is about 5 nm. The size distribution is in the narrow range and no agglomerates are observed. Y 2O 3 nanoparticles coated with DBS are easy to dissolve in weak polar solvents.
文摘Long afterglow phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） were synthesized by microemulsion method, and their crystal structure and luminescent properties were compared and investigated. XRD patterns of samples indicate that phosphors CaAl2O4：Eu^2＋, Dy^3＋ and SrAl2O4 ： Eu^2＋, Dy^3＋ are with monoelinie crystal structure and phosphor BaAl2O4：Eu^2＋ , Dy^3＋ is with hexagonal crystal structure. The wide range of excitation spectrum of phosphors MAl2O4： Eu^2 ＋ , Dy^3＋ （M = Ca,Sr, Ba） indicates that the luminescent materials can he excited by light from ultraviolet ray to visible light and the maximum emission wavelength of phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） is found mainly at λem of 440 nm （M = Ca）, 520 nm （M = Sr） and 496 nm （M = Ba） respectively, the corresponding colors of emission light are blue, green and eyna-green respectively. The afterglow decay tendency of phosphors can he summarized as three processes： initial rapid decay, intermediate transitional decay and very long slow decay. Afterglow decay curves coincide with formula I = At^ - n, and the sequence of afterglow intensity and time is Sr 〉 Ca 〉 Ba.
基金Projects(20601012,20601016,20961005)supported by the National Natural Science Foundation of ChinaProject(209024)supported by the Ministry of Education of ChinaProjects(206077,206043,10013-121008)supported by Inner Mongolia University,China
文摘A microemulsion-mediated hydrothermal method for synthesis of YVO4:RE(RE=Yb 3+/Er 3+,Yb 3+/Tm 3+)nanoparticles by hydrothermal treatment of quaternary microemulsion medium consisting of Na3VO4/NaOH and RE(NO3)3 aqueous solution, surfactant cetyltrimethylammonium bromide(CTAB),cosurfactant n-hexanol and oil phase n-heptane was report.The confinement of microemulsion droplets acting as microreactors during the reaction process allows the formation of small size YVO4:RE nanoparticles with relatively narrow size distribution and less aggregation.The structure,size and shape of YVO4:RE nanoparticles were investigated by means of X-ray diffractometry(XRD)and transmission electron microscopy(TEM).Compared with the conventional solid annealing diffusion method,the microemulsion-mediated hydrothermal method shows superiority in obtaining YVO4:RE nanoparticles with controllable size,narrow size distribution and less aggregation.The microemulsion-mediated hydrothermal method may be potentially applicable for synthesis of other rare earth doped up-converting luminescence nanomaterials.
文摘Polysiloxane latexes were prepared by microemulsion polymerization of octamethylcyclotetrasiloxane （D4） in the absence of co-emulsifier with octadecyl trimethyl ammonium chloride as a cationic emulsifier and potassium hydrate as an initiator. The particle size was determined by the dynamic light scattering （DLS） technique and the reaction rates of the polymerization were discussed. Furthermore, the kinetics was studied by an initial-rate method, and the effects of the monomer, emulsifier and initiator concentrations and the temperature on polymerization conversions were investigated. From the kinetic results, the rate of polymerization, Rp at 80℃ can be expressed as Rp = k[D4]^0.79 [OTAC]^0.64[KOH]^0.38 and the aonarent activation energy（Ea）. which was determined by half-period method, is 95.32 kJ mol^-1.
文摘Nanocrystalline TiO2 powders with high photocatalytic activity were prepared by one-step microemulsion-mediated hydrothermal method using tetrabutylorthotitanate (TiO(C4H9)4, TBOT) as precursor. The as-prepared TiO2 powders were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and the Brunauer-Emmett-Teller (BET) specific surface area measurements. The effects of the oil/water ratio and hydrothermal temperature on the microstructures and photocatalytic activity of the TiO2 powders were investigated. The results suggest that increasing the oil/water emulsion ratio significantly decreased the particle size of the as-prepared TiO2 powders and improved the photocatalytic activity. With hydrothermal temperature increasing, the average crystallite size increased and the photocatalytic activities of TiO2 powders decreased.
文摘The CeO_2-ZrO_2 solid solutions were prepared by a reverse microemulsion method. The effect of preparation parameters on the surface area and crystalline form of the solid solutions were studied by the BET surface area and XRD analysis. The studies indicate that the separation of the microemulsion phase during the preparation procedure can decrease the specific surface area of sample, adding hydrogen peroxide in the matrix solution can increase the specific surface area and stability of sample. The surface area of sample calcined at 550 ℃ for 5 h is 149 m^2·g^(-1), and that calcined at 900 ℃ for 6 h is 88 m^2·g^(-1). The sample with tetragonal symmetry Ce_(0.5)Zr_(0.5)O_2 phase has a higher stability.
基金the Natural Science Foundation Committee of China for the financial support (No.81173004 and No.81202483)
文摘In this study, the CaP/pDNA nanoparticles were prepared using Triton X-100/Butanol/Cyclohexane/Water reverse microemulsion system. Optimization of preparation conditions was based on evaluation of particle size by Box–Behnken design method. The particle sizes of the optimized CaP/pDNA nanoparticles were found to be 60.23 ± 4.72 nm, polydispersity index was 0.252 and pDNA encapsulate efficiency was more than 90%. The optimized CaP/pDNA nanoparticles have pH sensitivity and biocompatibility. Further, optimized CaP/pDNA nanoparticles showed higher transfection efficiency.
文摘Adsorption isotherm is the most fundamental information related to chromatography. To calculate the parameters of Langmuir ad-sorption isotherm of thymidine, frontal analysis (FA) and elution-curve method (ECM) were adopted in reversed-phase high performance liguid chromatography (RP-HPLC). In FA, the concentration of stationary phase was measured from the elution curves and the isotherm was deter-mined by regression analysis, while the parameters by ECM were obtained by parameter optimization. The adsorption isotherms of thymidine from the two methods were very similar. The superiority of ECM over FA was that the consumption of sample was less and only one or two in-jections of sample were required.
文摘A new microemulsion method using tetraoctylammonium bromide as a cationic surfactant has been formulated to fabricate thiol-functionalized gold nanoparticles, The nanoparticles were compared with those synthesized by the multistep Brust two-phase method.The nanoparticle sizes and size distributions fabricated by the two methods were characterized by UV-vis ahsorbance spectroscopy and transmittance electron microscopy. The simple microemulsion method produced the same results as those obtained by the Brust method,
