To get a better understanding of structural deactivation of ZSM-5/MOR during the catalytic cracking of n-heptane in the steam atmosphere, a comprehensive mechanism of hydrothermal dealumination was proposed through in...To get a better understanding of structural deactivation of ZSM-5/MOR during the catalytic cracking of n-heptane in the steam atmosphere, a comprehensive mechanism of hydrothermal dealumination was proposed through in-situ diffuse reflectance Fourier transform infrared spectroscopy(DRIFTS) in this work. The mechanism can be divided into two steps: firstly, the hydrolysis of four Al\\O bonds, and secondly, the self-healing of Si\\OH bonds accompanied with partial condensation of the extra-framework Al species. Accordingly, the kinetics of dealumination process has also been fully discussed. In the IR spectra, the range of 3450–3850 cm^(-1) could be deconvolved to distinguish the hydroxyl groups on the different position and calculate the consumption of each hydroxyl group during the reaction. Based on results from the in-situ DRIFTS, the kinetics of dealumination was hence developed and also in well agreement with the kinetics of deactivation of ZSM/MOR catalysts during the reaction in the presence of little coke deposits.展开更多
The mesoporous materials supported zirconium (Zr-MCM-48) and magnesium (Mg-MCM-48) with three-dimen- sional pore structures and different Zr or Mg contents were prepared via the hydrothermal method, respectively. ...The mesoporous materials supported zirconium (Zr-MCM-48) and magnesium (Mg-MCM-48) with three-dimen- sional pore structures and different Zr or Mg contents were prepared via the hydrothermal method, respectively. The prepared samples were characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), NH3 temperature programmed desorption (NH3-TPD) and N2 adsorption-desorption. The XRD, TEM and N2 adsorption-desorption results suggested that M-MCM-48 (where M = Zr, Mg) samples still maintained typical cubic mesoporous framework of MCM-48, with slight decrease of specific surface areas and mesopore orders. The isomerization of n-heptane was carried out as a probe reaction at various factors including the zirconium or magnesium content, reaction time, reaction temperature and weight hourly space veloc- ity (WHSV). Preliminary results demonstrated that the Mg-MCM-48 catalyst exhibited a higher catalytic activity with a maximum heptane conversion of 91.5% and a corresponding isomerization selectivity of 72.3% as compared to that of Zr- MCM-48. However, for catalytic stability of Mg-MCM-48 for n-heptane isomerization was poorer than Zr-MCM-48, because the Mg-MCM-48 catalyst could maintain a relatively high catalytic activity for only 130 rain, while the Zr-MCM-48 catalyst could maintain a relatively high catalytic activity for more than 190 min without any obvious decrease in performance.展开更多
Crystals of a new organometallic nonlinear optical (NLO) compound, di-ta-chloro-bis[chlorotri(thiourea)bismuth(Ⅲ)]- pentachloro(thiourea)bismuth-ate(Ⅲ) (DCBPB), have been successfully grown from formic a...Crystals of a new organometallic nonlinear optical (NLO) compound, di-ta-chloro-bis[chlorotri(thiourea)bismuth(Ⅲ)]- pentachloro(thiourea)bismuth-ate(Ⅲ) (DCBPB), have been successfully grown from formic acid aqueous solutions of thio-urea and bismuth chloride by a slow evaporation technique. The crystal structure and atomic composition of DCBPB have been confirmed by single crystal X-ray diffraction (SCXRD), Fourier transform infrared spectra, and elemental analysis. The SCXRD results proved that DCBPB crystallizes in triclinic space group P1 with unit cell dimensions of a = 7.0606(2) A, b = 8.8106(4) A, c = 16.3247(8) A, a = 99.242(4)°, fl = 95.309(3)°, )/= 105.856(3)°, and Z= 2. DCBPB crystal exhibits excel-lent transmittance from 500 to 2500 nm and green fluorescence with maximum emission at 508 nm. The thermogravimetric-differential scanning calorimetry (TG-DSC) analysis indicates that a solid-phase reaction took place at 170.1 ℃, whereas the decomposition temperature of the crystal material was 189℃. The NLO property obtained by the Kurtz powder test showed that the second harmonic generation efficiency of DCBPB crystal is two-seventh of KDP crystal.展开更多
In this study,polyvinyl alcohol(PVA)–ionic liquid(IL) membranes were prepared for the separation of isopropyl alcohol(IPA)–water azeotropic mixtures by pervaporation.PVA-IL composite membranes were prepared by simpl...In this study,polyvinyl alcohol(PVA)–ionic liquid(IL) membranes were prepared for the separation of isopropyl alcohol(IPA)–water azeotropic mixtures by pervaporation.PVA-IL composite membranes were prepared by simple solvent evaporation method using four ILs,viz.,1-n-butyl-3-methylimidazolium chloride(BMIMCl),1-hexyl-3-methylimidazolium chloride(HMIMCl),1-hexyl-3-methylimidazolium tetra fluoroborate(HMIMBF4) and 1-octyl-3-methylimidazolium chloride(OMIMCl).Three ILs were used to study the effect of alkyl chain on the pervaporation performance.The study had focused on the effect feed water concentration from 10%–40%and effect of feed temperature from 50–80°C.Physiochemical properties of all the membranes were studied using Fourier transform infrared spectroscopy(FTIR),scanning electron microscopy(SEM) and contact angle measurement.The Arrhenius activation energies for permeation were estimated to be in the range 4–12 kJ·mol-1 from the temperature dependent permeation values.展开更多
In this work, new composite membranes were successfully prepared via phase inversion technique using polyvinyl chloride(PVC) and polyvinylpyrrolidone(PVP) as polymers and tetrahydrofuran(THF) and N-methyl-2-pyrrolidon...In this work, new composite membranes were successfully prepared via phase inversion technique using polyvinyl chloride(PVC) and polyvinylpyrrolidone(PVP) as polymers and tetrahydrofuran(THF) and N-methyl-2-pyrrolidone(NMP) as solvents. The prepared membranes have been characterized by scanning electron microscope(SEM), and fourier transforms infrared spectroscopy(FTIR). The scanning electron microscope results prove that the prepared membranes are smooth and their pores are distributed throughout the whole surface and bulk body of the membrane without any visible cracks. The stress–strain mechanical test showed an excellent mechanical behavior enhanced by the presence of PVP in the prepared membranes. The membranes performance results showed that the salt rejection reached 98% with a high flux. This, in turn, makes the prepared membranes can be applied for sea and brackish water treatment through membrane distillation technology.展开更多
基金Supported by the National Key Research and Development Program of China(2016YFA0202900)the National Natural Science Foundation of China(91434123,21622606)+1 种基金Zhejiang Provincial Natural Science Foundation of China(LR18B060001)the Fundamental Research Funds for the Central Universities
文摘To get a better understanding of structural deactivation of ZSM-5/MOR during the catalytic cracking of n-heptane in the steam atmosphere, a comprehensive mechanism of hydrothermal dealumination was proposed through in-situ diffuse reflectance Fourier transform infrared spectroscopy(DRIFTS) in this work. The mechanism can be divided into two steps: firstly, the hydrolysis of four Al\\O bonds, and secondly, the self-healing of Si\\OH bonds accompanied with partial condensation of the extra-framework Al species. Accordingly, the kinetics of dealumination process has also been fully discussed. In the IR spectra, the range of 3450–3850 cm^(-1) could be deconvolved to distinguish the hydroxyl groups on the different position and calculate the consumption of each hydroxyl group during the reaction. Based on results from the in-situ DRIFTS, the kinetics of dealumination was hence developed and also in well agreement with the kinetics of deactivation of ZSM/MOR catalysts during the reaction in the presence of little coke deposits.
基金supported by the postdoctoral programme for chemical engineering and technology of Northeast Petroleum Universitythe Youth Fund of Northeast Petroleum University(grant number NEPUQN2015-1-08)+2 种基金the Cultivation Fund of Northeast Petroleum University [grant number 2017PYYL-03]the Daqing Science and Technology Plan Projects [grant number szdfy-2015-04]the College Students’ Innovative Entrepreneurial Training Plan Projects of Heilongjiang Province [grant number 201710220030]
文摘The mesoporous materials supported zirconium (Zr-MCM-48) and magnesium (Mg-MCM-48) with three-dimen- sional pore structures and different Zr or Mg contents were prepared via the hydrothermal method, respectively. The prepared samples were characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), NH3 temperature programmed desorption (NH3-TPD) and N2 adsorption-desorption. The XRD, TEM and N2 adsorption-desorption results suggested that M-MCM-48 (where M = Zr, Mg) samples still maintained typical cubic mesoporous framework of MCM-48, with slight decrease of specific surface areas and mesopore orders. The isomerization of n-heptane was carried out as a probe reaction at various factors including the zirconium or magnesium content, reaction time, reaction temperature and weight hourly space veloc- ity (WHSV). Preliminary results demonstrated that the Mg-MCM-48 catalyst exhibited a higher catalytic activity with a maximum heptane conversion of 91.5% and a corresponding isomerization selectivity of 72.3% as compared to that of Zr- MCM-48. However, for catalytic stability of Mg-MCM-48 for n-heptane isomerization was poorer than Zr-MCM-48, because the Mg-MCM-48 catalyst could maintain a relatively high catalytic activity for only 130 rain, while the Zr-MCM-48 catalyst could maintain a relatively high catalytic activity for more than 190 min without any obvious decrease in performance.
基金the support by the National Key Research and Development Program of China(No.2016YFC0400408)
文摘Crystals of a new organometallic nonlinear optical (NLO) compound, di-ta-chloro-bis[chlorotri(thiourea)bismuth(Ⅲ)]- pentachloro(thiourea)bismuth-ate(Ⅲ) (DCBPB), have been successfully grown from formic acid aqueous solutions of thio-urea and bismuth chloride by a slow evaporation technique. The crystal structure and atomic composition of DCBPB have been confirmed by single crystal X-ray diffraction (SCXRD), Fourier transform infrared spectra, and elemental analysis. The SCXRD results proved that DCBPB crystallizes in triclinic space group P1 with unit cell dimensions of a = 7.0606(2) A, b = 8.8106(4) A, c = 16.3247(8) A, a = 99.242(4)°, fl = 95.309(3)°, )/= 105.856(3)°, and Z= 2. DCBPB crystal exhibits excel-lent transmittance from 500 to 2500 nm and green fluorescence with maximum emission at 508 nm. The thermogravimetric-differential scanning calorimetry (TG-DSC) analysis indicates that a solid-phase reaction took place at 170.1 ℃, whereas the decomposition temperature of the crystal material was 189℃. The NLO property obtained by the Kurtz powder test showed that the second harmonic generation efficiency of DCBPB crystal is two-seventh of KDP crystal.
文摘In this study,polyvinyl alcohol(PVA)–ionic liquid(IL) membranes were prepared for the separation of isopropyl alcohol(IPA)–water azeotropic mixtures by pervaporation.PVA-IL composite membranes were prepared by simple solvent evaporation method using four ILs,viz.,1-n-butyl-3-methylimidazolium chloride(BMIMCl),1-hexyl-3-methylimidazolium chloride(HMIMCl),1-hexyl-3-methylimidazolium tetra fluoroborate(HMIMBF4) and 1-octyl-3-methylimidazolium chloride(OMIMCl).Three ILs were used to study the effect of alkyl chain on the pervaporation performance.The study had focused on the effect feed water concentration from 10%–40%and effect of feed temperature from 50–80°C.Physiochemical properties of all the membranes were studied using Fourier transform infrared spectroscopy(FTIR),scanning electron microscopy(SEM) and contact angle measurement.The Arrhenius activation energies for permeation were estimated to be in the range 4–12 kJ·mol-1 from the temperature dependent permeation values.
文摘In this work, new composite membranes were successfully prepared via phase inversion technique using polyvinyl chloride(PVC) and polyvinylpyrrolidone(PVP) as polymers and tetrahydrofuran(THF) and N-methyl-2-pyrrolidone(NMP) as solvents. The prepared membranes have been characterized by scanning electron microscope(SEM), and fourier transforms infrared spectroscopy(FTIR). The scanning electron microscope results prove that the prepared membranes are smooth and their pores are distributed throughout the whole surface and bulk body of the membrane without any visible cracks. The stress–strain mechanical test showed an excellent mechanical behavior enhanced by the presence of PVP in the prepared membranes. The membranes performance results showed that the salt rejection reached 98% with a high flux. This, in turn, makes the prepared membranes can be applied for sea and brackish water treatment through membrane distillation technology.