The mesoporous hydroxyapatite （HA） was synthesized by hydrothermal method utilizing cationic surfactant cetyltrimethylammonium bromide （CTAB） as template. The crystalline phase, morphology and porous structure wer...The mesoporous hydroxyapatite （HA） was synthesized by hydrothermal method utilizing cationic surfactant cetyltrimethylammonium bromide （CTAB） as template. The crystalline phase, morphology and porous structure were characterized respectively by different detecting techniques. The results reveal that the particles are highly crystalline hydroxyapatite phase. The surfactant has little influence on the morphology of the crystals, but affects the porous structure obviously. The sample without CTAB has a low surface area not exceeding 33 m^2/g, and no distinct pores can be observed by TEM. While the samples obtained with the surfactant get better parameters. Numerous open-ended pores centered at 2-7 nm spread unequally on the surface of the hydroxyapatite nanorods. The N2 adsorption-desorption experiments show type IV isotherms with distinct hysteresis loops, illustrating the presence of mesoporous structure. When the mole ratio of CTAB to HA is 1：2, the sample has the largest surface area of 97.1 m^2/g and pore volume of 0.466 cm^3/g.展开更多
Amine-functionalized mesoporous silica was prepared by using lauric acid and N-stearoyl-l-glutamic acid as structure directing agents via the S-N+-I- mechanism and applied to CO2 adsorption at room temperature. With ...Amine-functionalized mesoporous silica was prepared by using lauric acid and N-stearoyl-l-glutamic acid as structure directing agents via the S-N+-I- mechanism and applied to CO2 adsorption at room temperature. With γ-aminopropyltriethoxysilane as co-structure directing agent and due to the direct electrostatic interaction with anionic surfactant, most of the amino groups were uniformly distributed at the inner surface of pores and the per- formance was stable. The amine-functionalized mesoporous silica was characterized by Fourier transform infrared spectrometer, X-ray diffraction, nitrogen physisorption and thermogravimetric analysis. The CO2 adsorption capacity was measured by digital recording balance. At the room temperature and under the atmospheric pressure, the adsorption capacity of LAA-AMS-0.2 for CO2 and N2 is 1.40 mmol·g-1 and 0.03 mmol·g-1, respectively, indicating high separation coefficient of CO2/N2.展开更多
By varying concentration of PEG1000 as a structure-directing agent,mesoporous alumina with excellent textural properties was synthesized.The prepared mesoporous alumina displays high thermal stability,as shown by its ...By varying concentration of PEG1000 as a structure-directing agent,mesoporous alumina with excellent textural properties was synthesized.The prepared mesoporous alumina displays high thermal stability,as shown by its textural properties at different calcination temperatures of 600-850 °C.Characterization by SEM and TEM revealed that the added PEG surfactant induced the formation of petal-like alumina.XRD results clarified that all samples were amorphous and their peaks were around the peaks of γ-alumina.N_2 adsorption-desorption analysis showed that the prepared mesoporous alumina,if with PEG1000 in hydrolysis of aluminum isopropoxide,had excellent textural properties with large specific surface area,high pore volume and suitable pore size.The petal-like structure existing in the alumina samples improved their textural parameters,and the role and influential mechanism of PEG1000 were analyzed.展开更多
The properties of aqueous two-phase system (ATPS) of mixed solution containing gemini cationic surfactant trimethylene-1,3-bis(dodecyldimethyl ammonium) bromide (12-3-12, 2Br-) and traditional anionic surfactant sodiu...The properties of aqueous two-phase system (ATPS) of mixed solution containing gemini cationic surfactant trimethylene-1,3-bis(dodecyldimethyl ammonium) bromide (12-3-12, 2Br-) and traditional anionic surfactant sodium dodecyl sulfate (SDS) with or without added salt have been studied. An ATPS is formed in a narrow region of the ternary phase diagram different from that of traditional aqueous cationic-anionic surfactant systems. In ATPS region, the lowest total concentration of surfactants varies with the mixing ratio of geminis to SDS. Photographs obtained from freeze-etching, negative-staining and transmission electron microscopy show that the microstructures of two phases are different from each other. Micelles and vesicles can coexist in a single phase. The addition of salts can change the phase diagram of ATPS. Furthermore, the added salts promote the aggregation of rod-like micelles to form coarse network structure that increase the viscosity of solutions. The negative ions of the added salts are the determining factor.展开更多
The forming mechanism of microemulsion of sodium dodecyl sulfonate, alcohols,water and isooctane was studied, with particular emphasis on the effect of molecular weight andconcentration of alcohols. Phase diagram of t...The forming mechanism of microemulsion of sodium dodecyl sulfonate, alcohols,water and isooctane was studied, with particular emphasis on the effect of molecular weight andconcentration of alcohols. Phase diagram of the four components, alcohol, sodium dodecyl sulfonate,water and isooctane, was used as a means of study, through which the microemulsion regions weredetermined. Phase diagram of sodium dodecyl sulfonate/n-pentanol/isooctane/water system at κ_m = 2(κ_m = W_(n-pentanol)/W_(SDS)) is presented. The variation of conductivities of differentmicroemulsion samples with water was measured. From the conductivities we investigated a change instructure from water droplets in oil (W/O) at low water content to liquid crystal at intermediatewater content and a stricture of oil droplets in water (O/W) at high water content.展开更多
In this study, X-ray diffraction （XRD）, Fourier transform infrared spectrometer （FTIR） together with Scanning probe microscopy （SPM） were used to characterize the structure and morphology of the complexes, where...In this study, X-ray diffraction （XRD）, Fourier transform infrared spectrometer （FTIR） together with Scanning probe microscopy （SPM） were used to characterize the structure and morphology of the complexes, where the hydrobiotites （Xinfiang） were modified by single-chain surfactants octyltrimethylammonium bromide （OTMA） and octadecyltrimethylammonium bromide （ODTMA）. XRD patterns showed that the structure of complexes was significantly influenced by the surfactant concentration and the alkyl chain length, because obvious changes took place in the basal spacing. Furthermore, according to the XRD results, several arrangements of surfactant molecules within the hydrobiotite interlayer space were deduced. The FTIR spectrum indicated that the surfactant contents in complexes dramatically increased with the alkyl chain length. The SPM micrographs demonstrated that the surfaces of complexes prepared at lower surfactant concentration were relatively flat compared with that prepared at higher concentration, while those with higher surfactant concentration had much steeper surface due to the alkyl chain length. It was concluded that structure and morphology of surfactant/hydrobiotite complexes depend not only on the surfactant concentration, but also strongly on the surfactant species.展开更多
Superhydrophobic and superhydrophilic surfaces have been extensively inves- tigated due to their importance for industrial applications. It has been reported, however, that superhydrophobic surfaces are very sensitive...Superhydrophobic and superhydrophilic surfaces have been extensively inves- tigated due to their importance for industrial applications. It has been reported, however, that superhydrophobic surfaces are very sensitive to heat, ultraviolet （UV） light, and electric potential, which interfere with their long-term durability. In this study, we introduce a novel approach to achieve robust superhydrophobic thin films by designing architecture-defined complex nanostructures. A family of ZnO hollow microspheres with controlled constituent architectures in the morphologies of 1D nanowire networks, 2D nanosheet stacks, and 3D mesoporous nanoball blocks, respectively, was synthesized via a two-step self-assembly approach, where the oligomers or the constituent nanostructures with specially designed structures are first formed from surfactant templates, and then further assembled into complex morphologies by the addition of a second co-surfactant. The thin films composed of two-step synthesized ZnO hollow microspheres with different architectures presented superhydrophobicities with contact angles of 150°-155°, superior to the contact angle of 103° for one-step synthesized ZnO hollow microspheres with smooth and solid surfaces. Moreover, the robust superhydrophobicity was further improved by perfluorinated silane surface modification. The perfluorinated silane treated ZnO hollow microsphere thin films maintained excellent hydrophobicity even after 75 h of UV irradiation. The realization of environmentally durable promising solution for their long-term irradiations. superhydrophobic surfaces provides a service under UV or strong solar light展开更多
Manganese selenide （MnSe） possesses unique magnetic properties as an important magnetic semiconductor, but the synthesis and properties of MnSe nanocrystals are less developed compared to other semiconductor nanocry...Manganese selenide （MnSe） possesses unique magnetic properties as an important magnetic semiconductor, but the synthesis and properties of MnSe nanocrystals are less developed compared to other semiconductor nanocrystals because of the inability to obtain high-quality MnSe, especially in the metastable wurtzite structure. Here, we have successfully fabricated wurtzite MnSe nanocrystals via a colloidal approach which affords uniform crystal sizes and tailored shapes. The selective binding strength of the amine surfactant is the determining factor in shape-control and shape-evolution. Bullet-shapes could be transformed into shuttle-shapes if part of the oleylamine in the reaction solution was replaced by trioctylamine, and tetrapod-shaped nanocrystals could be formed in trioctylamine systems. The three-dimensional （3D） structure of the bullet-shaped nanorods has been demonstrated by the advanced transmission electron microscope （TEM） 3D-tomography technology. High-resolution TEM （HRTEM） and electron energy-loss spectroscopy （EELS） show that planar-defect structures such as stacking faults and twinning along the [001] direction arise during the growth of bullet-shapes. On the basis of careful HRTEM observations, we propose a ＂quadra-twin core＂ growth mechanism for the formation of wurtzite MnSe nanotetrapods. Furthermore, the wurtzite MnSe nanocrystals show low- temperature surface spin-glass behavior due to their noncompensated surface spins and the blocking temperatures increase from 8.4 K to 18.5 K with increasing surface area/volume ratio of the nanocrystals. Our results provide a systematic study of wurtzite MnSe nanocrystals.展开更多
基金Projects(51102285,81170912)supported by the National Natural Science Foundation of ChinaProject supported by the Open Foundation of State Key Laboratory of Powder Metallurgy,China
文摘The mesoporous hydroxyapatite （HA） was synthesized by hydrothermal method utilizing cationic surfactant cetyltrimethylammonium bromide （CTAB） as template. The crystalline phase, morphology and porous structure were characterized respectively by different detecting techniques. The results reveal that the particles are highly crystalline hydroxyapatite phase. The surfactant has little influence on the morphology of the crystals, but affects the porous structure obviously. The sample without CTAB has a low surface area not exceeding 33 m^2/g, and no distinct pores can be observed by TEM. While the samples obtained with the surfactant get better parameters. Numerous open-ended pores centered at 2-7 nm spread unequally on the surface of the hydroxyapatite nanorods. The N2 adsorption-desorption experiments show type IV isotherms with distinct hysteresis loops, illustrating the presence of mesoporous structure. When the mole ratio of CTAB to HA is 1：2, the sample has the largest surface area of 97.1 m^2/g and pore volume of 0.466 cm^3/g.
基金Supported by Tianjin Hi-tech Support Program Key Projects, China (2009F3-0005)
文摘Amine-functionalized mesoporous silica was prepared by using lauric acid and N-stearoyl-l-glutamic acid as structure directing agents via the S-N+-I- mechanism and applied to CO2 adsorption at room temperature. With γ-aminopropyltriethoxysilane as co-structure directing agent and due to the direct electrostatic interaction with anionic surfactant, most of the amino groups were uniformly distributed at the inner surface of pores and the per- formance was stable. The amine-functionalized mesoporous silica was characterized by Fourier transform infrared spectrometer, X-ray diffraction, nitrogen physisorption and thermogravimetric analysis. The CO2 adsorption capacity was measured by digital recording balance. At the room temperature and under the atmospheric pressure, the adsorption capacity of LAA-AMS-0.2 for CO2 and N2 is 1.40 mmol·g-1 and 0.03 mmol·g-1, respectively, indicating high separation coefficient of CO2/N2.
基金Supported by the National Basic Research Program of China(Y419012198)the National Natural Science Foundation of China(No.91534125)
文摘By varying concentration of PEG1000 as a structure-directing agent,mesoporous alumina with excellent textural properties was synthesized.The prepared mesoporous alumina displays high thermal stability,as shown by its textural properties at different calcination temperatures of 600-850 °C.Characterization by SEM and TEM revealed that the added PEG surfactant induced the formation of petal-like alumina.XRD results clarified that all samples were amorphous and their peaks were around the peaks of γ-alumina.N_2 adsorption-desorption analysis showed that the prepared mesoporous alumina,if with PEG1000 in hydrolysis of aluminum isopropoxide,had excellent textural properties with large specific surface area,high pore volume and suitable pore size.The petal-like structure existing in the alumina samples improved their textural parameters,and the role and influential mechanism of PEG1000 were analyzed.
基金the National Natural Science Foundation of China (No. 20025618, No. 20236010) Shanghai Municipal Education Commission of China.
文摘The properties of aqueous two-phase system (ATPS) of mixed solution containing gemini cationic surfactant trimethylene-1,3-bis(dodecyldimethyl ammonium) bromide (12-3-12, 2Br-) and traditional anionic surfactant sodium dodecyl sulfate (SDS) with or without added salt have been studied. An ATPS is formed in a narrow region of the ternary phase diagram different from that of traditional aqueous cationic-anionic surfactant systems. In ATPS region, the lowest total concentration of surfactants varies with the mixing ratio of geminis to SDS. Photographs obtained from freeze-etching, negative-staining and transmission electron microscopy show that the microstructures of two phases are different from each other. Micelles and vesicles can coexist in a single phase. The addition of salts can change the phase diagram of ATPS. Furthermore, the added salts promote the aggregation of rod-like micelles to form coarse network structure that increase the viscosity of solutions. The negative ions of the added salts are the determining factor.
基金Supported by the Natural Science Foundation of Zhejiang Province (No. 299018).
文摘The forming mechanism of microemulsion of sodium dodecyl sulfonate, alcohols,water and isooctane was studied, with particular emphasis on the effect of molecular weight andconcentration of alcohols. Phase diagram of the four components, alcohol, sodium dodecyl sulfonate,water and isooctane, was used as a means of study, through which the microemulsion regions weredetermined. Phase diagram of sodium dodecyl sulfonate/n-pentanol/isooctane/water system at κ_m = 2(κ_m = W_(n-pentanol)/W_(SDS)) is presented. The variation of conductivities of differentmicroemulsion samples with water was measured. From the conductivities we investigated a change instructure from water droplets in oil (W/O) at low water content to liquid crystal at intermediatewater content and a stricture of oil droplets in water (O/W) at high water content.
基金NSFC (No. 40502008)Sichuan Province Application and Basic Research Project (No. 05JY029-008)
文摘In this study, X-ray diffraction （XRD）, Fourier transform infrared spectrometer （FTIR） together with Scanning probe microscopy （SPM） were used to characterize the structure and morphology of the complexes, where the hydrobiotites （Xinfiang） were modified by single-chain surfactants octyltrimethylammonium bromide （OTMA） and octadecyltrimethylammonium bromide （ODTMA）. XRD patterns showed that the structure of complexes was significantly influenced by the surfactant concentration and the alkyl chain length, because obvious changes took place in the basal spacing. Furthermore, according to the XRD results, several arrangements of surfactant molecules within the hydrobiotite interlayer space were deduced. The FTIR spectrum indicated that the surfactant contents in complexes dramatically increased with the alkyl chain length. The SPM micrographs demonstrated that the surfaces of complexes prepared at lower surfactant concentration were relatively flat compared with that prepared at higher concentration, while those with higher surfactant concentration had much steeper surface due to the alkyl chain length. It was concluded that structure and morphology of surfactant/hydrobiotite complexes depend not only on the surfactant concentration, but also strongly on the surfactant species.
基金Acknowledgements This work was supported by the Australian Research Council （ARC） Discovery Project No. DP1096546. ZQS was supported by an ARC Postdoctoral （APD） Research Fellowship and a University of Wollongong （UOW） Vice-chancellor＇s Research Fellowship. TL acknowledges the support of a University of Queensland （UQ） Postdoctoral Fellowship. KSL and LJ appreciate the financial support of the National Natural Science Foundation of China （Nos. 21273016, 21001013, and 20974113）, the National Basic Research Program of China （No. 2013CB933003）, the Program for New Century Excellent Talents in Universities, Beijing Natural Science Foundation （No. 2122035）, and the Key Research Program of the Chinese Academy of Sciences （No. KJZDEW-M01）.
文摘Superhydrophobic and superhydrophilic surfaces have been extensively inves- tigated due to their importance for industrial applications. It has been reported, however, that superhydrophobic surfaces are very sensitive to heat, ultraviolet （UV） light, and electric potential, which interfere with their long-term durability. In this study, we introduce a novel approach to achieve robust superhydrophobic thin films by designing architecture-defined complex nanostructures. A family of ZnO hollow microspheres with controlled constituent architectures in the morphologies of 1D nanowire networks, 2D nanosheet stacks, and 3D mesoporous nanoball blocks, respectively, was synthesized via a two-step self-assembly approach, where the oligomers or the constituent nanostructures with specially designed structures are first formed from surfactant templates, and then further assembled into complex morphologies by the addition of a second co-surfactant. The thin films composed of two-step synthesized ZnO hollow microspheres with different architectures presented superhydrophobicities with contact angles of 150°-155°, superior to the contact angle of 103° for one-step synthesized ZnO hollow microspheres with smooth and solid surfaces. Moreover, the robust superhydrophobicity was further improved by perfluorinated silane surface modification. The perfluorinated silane treated ZnO hollow microsphere thin films maintained excellent hydrophobicity even after 75 h of UV irradiation. The realization of environmentally durable promising solution for their long-term irradiations. superhydrophobic surfaces provides a service under UV or strong solar light
文摘Manganese selenide （MnSe） possesses unique magnetic properties as an important magnetic semiconductor, but the synthesis and properties of MnSe nanocrystals are less developed compared to other semiconductor nanocrystals because of the inability to obtain high-quality MnSe, especially in the metastable wurtzite structure. Here, we have successfully fabricated wurtzite MnSe nanocrystals via a colloidal approach which affords uniform crystal sizes and tailored shapes. The selective binding strength of the amine surfactant is the determining factor in shape-control and shape-evolution. Bullet-shapes could be transformed into shuttle-shapes if part of the oleylamine in the reaction solution was replaced by trioctylamine, and tetrapod-shaped nanocrystals could be formed in trioctylamine systems. The three-dimensional （3D） structure of the bullet-shaped nanorods has been demonstrated by the advanced transmission electron microscope （TEM） 3D-tomography technology. High-resolution TEM （HRTEM） and electron energy-loss spectroscopy （EELS） show that planar-defect structures such as stacking faults and twinning along the [001] direction arise during the growth of bullet-shapes. On the basis of careful HRTEM observations, we propose a ＂quadra-twin core＂ growth mechanism for the formation of wurtzite MnSe nanotetrapods. Furthermore, the wurtzite MnSe nanocrystals show low- temperature surface spin-glass behavior due to their noncompensated surface spins and the blocking temperatures increase from 8.4 K to 18.5 K with increasing surface area/volume ratio of the nanocrystals. Our results provide a systematic study of wurtzite MnSe nanocrystals.
