An efficient synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is achieved via a reaction of acenaphthe-nequinone and indoles catalyzed by solid superacid SO4^2-/TiO2 under solvent-free conditions...An efficient synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is achieved via a reaction of acenaphthe-nequinone and indoles catalyzed by solid superacid SO4^2-/TiO2 under solvent-free conditions at room temperature by grinding, which provides an efficient route to the synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one.This procedure offers several advantages including solvent-free conditions,excellent yields of products,simple work-up as well as reuse of catalysts which makes it a useful and attractive protocol for the synthesis of these compounds.展开更多
The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1...The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1). the CPC-12 conversion at 310C over Ti(SO_4)_2 calcined at 350C remained about 98.5% during 360 h on stream. and the selectivity to by-products remained zero. The findings enlarged the scope of traditional catalyst systems for the CFCs decomposition.展开更多
Using two piezoelectric transducers, one measures the stress tensor response from the strain field generated by the second transducer. The ratio between the stress response and strain velocity determines the dissipati...Using two piezoelectric transducers, one measures the stress tensor response from the strain field generated by the second transducer. The ratio between the stress response and strain velocity determines the dissipative response. In the first part, we show that the dissipative stress response can be used for studying excitations in a topological superconductor. We investigate a topological superconductor for the case when an Abrikosov vortex lattice is formed. In this case, the Majorana fermions are dispersive, a fact that is used to compute the dissipative stress response. In the second part, we analyse the dissipative superfluid flow through solid 4He discoused recently. We identify low energy, an excitation which plays the role of the Majorana mode which is free to move in a direction perpendicular to the two dimensional plane spaces of the dislocations.展开更多
Ag3PO4 microcrystals with highly enhanced visible light photocatalytic activity are prepared by a facile and simple solid state reaction at room temperature. The composition, morphology and optical properties of the a...Ag3PO4 microcrystals with highly enhanced visible light photocatalytic activity are prepared by a facile and simple solid state reaction at room temperature. The composition, morphology and optical properties of the asprepared Ag3PO4 microcrystMs are characterized by x-ray diffraction, scanning electron microscopy and UV-vis diffuse reflectance spectra. The photocatalytie properties of Ag3PO4 are investigated by the degradation of both methylene blue and methyl orange dyes under visible light irradiation. The as-prepared Ag3PO4 microcrystals possess high photocatalytic oxygen production with the rate of 673μmolh-1g-1. Moreover, the as-prepared Ag3PO4 microcrystals show an enhanced photoelectrochemistry performance under irradiation of visible light.展开更多
Dispersion of KF on AlPO4-5 molecular sieve created basic sites and caused 1654 cm- band of bidentate carbonate in CO2 adsorption.After pre-treated above 823K. 5%KF/AlPO4-5exhibited basic catalytic activity in the iso...Dispersion of KF on AlPO4-5 molecular sieve created basic sites and caused 1654 cm- band of bidentate carbonate in CO2 adsorption.After pre-treated above 823K. 5%KF/AlPO4-5exhibited basic catalytic activity in the isomerization of butenes at 273K. and the activity increasedwith the pre-treatment temperature up to 923K.展开更多
Nowadays,the majority of the studies on the substitution are focused on cations(such as Y^(3+),Ti^(4+),P^(5+),etc.)in Li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP),while there are few studies on the substitution of anion...Nowadays,the majority of the studies on the substitution are focused on cations(such as Y^(3+),Ti^(4+),P^(5+),etc.)in Li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP),while there are few studies on the substitution of anion O^(2-).In this work,the modified LATP with a series of LiCl(LATPClx,x=0.1,0.2,0.3,0.4)additives is prepared to enhance ionic conductivity.The successful introduction of Cl-makes the length of the c axis decrease from 20.822(2)to 20.792(1)Å,and the bulk conductivity of 2.13×10^(-3) S·cm^(-1) is achieved in LATPCl_(0.3).Moreover,the Al/Ti-O1/Cl1 and Al/Ti-O_(2)/Cl_(2) distance decrease,while the Li1-O_(2)/Cl_(2) distance increases.Lithium ions migrate more easily in the nanochannel of M3-M1-M3.In addition,the LiCl additive increases the relative density and the grain boundary conductivity of LATPClx compounds.Naturally,a higher ionic conductivity of 2.12×10^(–4) S·cm^(-1) and a low activation energy of 0.30 eV are obtained in LATPCl_(0.3).Correspondingly,the symmetric cell exhibits a low overpotential of±50 mV for over 200 h in LATPCl_(0.3).The solid-state Li|LATPCl_(0.3)|NCM811(NCM811=LiNi0.8Co0.1Mn0.1O_(2))battery exhibits high initial capacity 185.1 mAh·g^(-1) with a capacity retention rate of 95.4%after 100 cycles at 0.5 C.This result suggests that LiCl additive is an effective strategy to promote electrochemical properties of LATP solid electrolyte and can be considered for reference to other inorganic solid electrolytes systems.展开更多
A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) method is described for determination of letrozole in human plasma.Following solid phase extraction(SPE) of letroz...A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) method is described for determination of letrozole in human plasma.Following solid phase extraction(SPE) of letrozole and letrozole-d4 on Orochem DVB-LP cartridges,chromatography was performed on Acquity UPLC BEH C_(18)(50 mm × 2.1 mm.1.7 μm) column using methanol-0.1%formic acid in water(85:15,v/v) as the mobile phase.Detection was carried out on a triple quadrupole mass spectrometer with an electrospray source,operated under positive ionization mode.Quantitation of letrozole and letrozole-d4 was done using multiple reaction monitoring(MRM) following the transitions at m/z286.2→217.0 and m/z 290.2→221.0,respectively.The calibration plots were linear through the concentration range of 0.10-100 ng/mL(r^2 ≥ 0.9990) using 100 μL human plasma.The extraction recovery of letrozole ranged from 94.3%to 96.2%and the intra-batch and inter-batch precision was ≤ 5.2%.The method was successfully applied to a bioequivalence study of letrozole after oral administration of2.5 mg tablet formulation to 16 healthy postmenopausal Indian women.The assay reproducibility was also established through incurred sample reanalysis(ISR) of 74 subject samples.展开更多
Solid complex Zn(Thr)SO 4·H 2O was prepared in a water acetone system. Under linearly increasing temperature, the non isothermal kinetics and the decomposition mechanism of Zn(Thr)SO 4·H 2O were studie...Solid complex Zn(Thr)SO 4·H 2O was prepared in a water acetone system. Under linearly increasing temperature, the non isothermal kinetics and the decomposition mechanism of Zn(Thr)SO 4·H 2O were studied by means of thermogravimetry and IR spectrometry. The thermal decomposition processes of the complex could be divided into three stages. The non isothermal decomposition mechanism and the kinetics parameters of the ligand lost process were obtained from an analysis to the TG DTG curves at various heating rates of 5 0, 10 0, 15 0 and 20 0 K/min by two integral and three differential methods. The results show that the random nucleation and the subsequent growth mechanism ( n =3/2) controlled the ligand lost process, the corresponding activation energy E and pre exponential constant A are 139 96 kJ/mol and 10 11 32 s -1 , respectively. The empirical kinetics model equation was constructed.展开更多
Series Bi3NbO7/Bi2Zn(2/3)Nb(4/3)O7 (BN/BZN) composites were synthesized through a facile solid state reaction method. The products were characterized by X-ray diffraction(XRD), field emission scanning electron...Series Bi3NbO7/Bi2Zn(2/3)Nb(4/3)O7 (BN/BZN) composites were synthesized through a facile solid state reaction method. The products were characterized by X-ray diffraction(XRD), field emission scanning electron microscopy(FE-SEM) and UV-vis diffuse reflectance spectroscopy(DRS). When BN: BZN=0.1 mole ratio, the BN/BZN composite showed the best visible-light-driven photocatalytic performance, which decomposed nearly 100% of Rh B(10 ppm, p H=3-4) within 40 min. The results demonstrated that in-situ solid state synthesis of BN/BZN composites could be an efficient strategy to develop new photocatalyst for environmental remediation.展开更多
Hot compressive experiments of the laser solid formed(LSFed)TC4 titanium alloy were conducted at a wide temperature range of 650-950℃and strain rate of 0.01-10 s^(-1).The Arrheniustype constitutive models of the LSFe...Hot compressive experiments of the laser solid formed(LSFed)TC4 titanium alloy were conducted at a wide temperature range of 650-950℃and strain rate of 0.01-10 s^(-1).The Arrheniustype constitutive models of the LSFed TC4 alloy were established at the temperature range of 800-950℃and of 650-800℃,respectively.The average relative error between the predicted stresses and experimental values in those two temperature ranges are 10.4%and 8.3%,respectively,indicating that the prediction models constructed in this paper are in a good agreement with experimental data.Processing maps were established by the principle of dynamic materials modeling on the basis of the data achieved from the hot compression experiments.The processing parameters corresponding to the stable and unstable regions of material deformation can be determined from the processing maps.The microstructure evolution of the stable and unstable regions of the samples after tests were observed.Finally,the effect of hot compressive parameters on the microstructure were investigated to research the dynamic recrystallization and the texture of the deformed LSFed TC4 alloy.展开更多
A novel, high-temperature, mechano-chemical(HTMC) method was developed to synthesise singlephase Sr_2CeO_4:Eu^(3+)phosphor. Phosphors were characterised by X-ray diffraction(XRD), scanning electron microscopy...A novel, high-temperature, mechano-chemical(HTMC) method was developed to synthesise singlephase Sr_2CeO_4:Eu^(3+)phosphor. Phosphors were characterised by X-ray diffraction(XRD), scanning electron microscopy(SEM), and luminescence spectra. Compared with phosphors prepared by the traditional hightemperature solid state method and citric acid gel method, single-phase Sr_2CeO_4:Eu^(3+)powders by using the HTMC method, with small average particle sizes of about 5 μm, a narrow size distribution range and uniform dispersion, were prepared at 800 ℃, and reached their maximum luminescent intensity at 900 ℃.Under ultraviolet excitation at 298 nm, the sample showed good luminescence with the strongest red light of 616 nm. However, Sr_2CeO_4:Eu^(3+)was prepared at the higher temperature of 1100 ℃ by solid state method and citric acid gel method. The particle size was too large and uneven with phosphor agglomeration by high-temperature solid state method. The luminescent intensity reached a maximum for Sr_2CeO_4:Eu^(3+)phosphor at a synthesis temperature of 1100 ℃ by using the high-temperature solid state method, and at 1200 ℃ by both citric acid gel and chemical precipitation methods. Furthermore, the advantages of the Sr_2CeO_4:Eu^(3+)powder prepared by HTMC method were discussed compared with that prepared using traditional high-temperature solid state and citric acid gel methods.展开更多
基金supported by the research foundation of Hebei University of Science and Technology
文摘An efficient synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is achieved via a reaction of acenaphthe-nequinone and indoles catalyzed by solid superacid SO4^2-/TiO2 under solvent-free conditions at room temperature by grinding, which provides an efficient route to the synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one.This procedure offers several advantages including solvent-free conditions,excellent yields of products,simple work-up as well as reuse of catalysts which makes it a useful and attractive protocol for the synthesis of these compounds.
文摘The catalytic hydrolysis of dichlorodifluoromethane (CFC-12) was investigated over solid acid Ti(SO_4)_2. The catalytic activity decreased with the calcination temperature. When space velocity was 6 1 h^(-1) g-cat^(-1). the CPC-12 conversion at 310C over Ti(SO_4)_2 calcined at 350C remained about 98.5% during 360 h on stream. and the selectivity to by-products remained zero. The findings enlarged the scope of traditional catalyst systems for the CFCs decomposition.
文摘Using two piezoelectric transducers, one measures the stress tensor response from the strain field generated by the second transducer. The ratio between the stress response and strain velocity determines the dissipative response. In the first part, we show that the dissipative stress response can be used for studying excitations in a topological superconductor. We investigate a topological superconductor for the case when an Abrikosov vortex lattice is formed. In this case, the Majorana fermions are dispersive, a fact that is used to compute the dissipative stress response. In the second part, we analyse the dissipative superfluid flow through solid 4He discoused recently. We identify low energy, an excitation which plays the role of the Majorana mode which is free to move in a direction perpendicular to the two dimensional plane spaces of the dislocations.
基金Supported by the Beijing Higher Education Young Elite Teacher Project under Grant No YETP1297the Fundamental Research Funds for the Central Universities under Grant No 2014MDLXYZY05+1 种基金the Undergraduate Innovative Test Program of China under Grant Nos GCCX2015110009 and BEIJ2015110024the National Natural Science Foundation of China under Grant Nos11074312 and 11374377
文摘Ag3PO4 microcrystals with highly enhanced visible light photocatalytic activity are prepared by a facile and simple solid state reaction at room temperature. The composition, morphology and optical properties of the asprepared Ag3PO4 microcrystMs are characterized by x-ray diffraction, scanning electron microscopy and UV-vis diffuse reflectance spectra. The photocatalytie properties of Ag3PO4 are investigated by the degradation of both methylene blue and methyl orange dyes under visible light irradiation. The as-prepared Ag3PO4 microcrystals possess high photocatalytic oxygen production with the rate of 673μmolh-1g-1. Moreover, the as-prepared Ag3PO4 microcrystals show an enhanced photoelectrochemistry performance under irradiation of visible light.
文摘Dispersion of KF on AlPO4-5 molecular sieve created basic sites and caused 1654 cm- band of bidentate carbonate in CO2 adsorption.After pre-treated above 823K. 5%KF/AlPO4-5exhibited basic catalytic activity in the isomerization of butenes at 273K. and the activity increasedwith the pre-treatment temperature up to 923K.
基金supported by the National Natural Science Foundation of China(NSFC)(Nos.51772239,51972262 and 22005186)the 111 Project(No.B14040).
文摘Nowadays,the majority of the studies on the substitution are focused on cations(such as Y^(3+),Ti^(4+),P^(5+),etc.)in Li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP),while there are few studies on the substitution of anion O^(2-).In this work,the modified LATP with a series of LiCl(LATPClx,x=0.1,0.2,0.3,0.4)additives is prepared to enhance ionic conductivity.The successful introduction of Cl-makes the length of the c axis decrease from 20.822(2)to 20.792(1)Å,and the bulk conductivity of 2.13×10^(-3) S·cm^(-1) is achieved in LATPCl_(0.3).Moreover,the Al/Ti-O1/Cl1 and Al/Ti-O_(2)/Cl_(2) distance decrease,while the Li1-O_(2)/Cl_(2) distance increases.Lithium ions migrate more easily in the nanochannel of M3-M1-M3.In addition,the LiCl additive increases the relative density and the grain boundary conductivity of LATPClx compounds.Naturally,a higher ionic conductivity of 2.12×10^(–4) S·cm^(-1) and a low activation energy of 0.30 eV are obtained in LATPCl_(0.3).Correspondingly,the symmetric cell exhibits a low overpotential of±50 mV for over 200 h in LATPCl_(0.3).The solid-state Li|LATPCl_(0.3)|NCM811(NCM811=LiNi0.8Co0.1Mn0.1O_(2))battery exhibits high initial capacity 185.1 mAh·g^(-1) with a capacity retention rate of 95.4%after 100 cycles at 0.5 C.This result suggests that LiCl additive is an effective strategy to promote electrochemical properties of LATP solid electrolyte and can be considered for reference to other inorganic solid electrolytes systems.
基金Department of Chemistry,St.Xavier's College,Ahmedabad,India for supporting this work
文摘A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) method is described for determination of letrozole in human plasma.Following solid phase extraction(SPE) of letrozole and letrozole-d4 on Orochem DVB-LP cartridges,chromatography was performed on Acquity UPLC BEH C_(18)(50 mm × 2.1 mm.1.7 μm) column using methanol-0.1%formic acid in water(85:15,v/v) as the mobile phase.Detection was carried out on a triple quadrupole mass spectrometer with an electrospray source,operated under positive ionization mode.Quantitation of letrozole and letrozole-d4 was done using multiple reaction monitoring(MRM) following the transitions at m/z286.2→217.0 and m/z 290.2→221.0,respectively.The calibration plots were linear through the concentration range of 0.10-100 ng/mL(r^2 ≥ 0.9990) using 100 μL human plasma.The extraction recovery of letrozole ranged from 94.3%to 96.2%and the intra-batch and inter-batch precision was ≤ 5.2%.The method was successfully applied to a bioequivalence study of letrozole after oral administration of2.5 mg tablet formulation to 16 healthy postmenopausal Indian women.The assay reproducibility was also established through incurred sample reanalysis(ISR) of 74 subject samples.
基金Supported by the National Natural Science Foundation of China(No.2 98710 32 and2 0 1710 36 ) and the EducationalSpecial Foundation of Shaanxi Province(No.0 1H0 8)
文摘Solid complex Zn(Thr)SO 4·H 2O was prepared in a water acetone system. Under linearly increasing temperature, the non isothermal kinetics and the decomposition mechanism of Zn(Thr)SO 4·H 2O were studied by means of thermogravimetry and IR spectrometry. The thermal decomposition processes of the complex could be divided into three stages. The non isothermal decomposition mechanism and the kinetics parameters of the ligand lost process were obtained from an analysis to the TG DTG curves at various heating rates of 5 0, 10 0, 15 0 and 20 0 K/min by two integral and three differential methods. The results show that the random nucleation and the subsequent growth mechanism ( n =3/2) controlled the ligand lost process, the corresponding activation energy E and pre exponential constant A are 139 96 kJ/mol and 10 11 32 s -1 , respectively. The empirical kinetics model equation was constructed.
基金Funded by the National Natural Science Foundation of China(No.51662005)the Guangxi Natural Science Foundation(No.2014GXNSFFA118004)
文摘Series Bi3NbO7/Bi2Zn(2/3)Nb(4/3)O7 (BN/BZN) composites were synthesized through a facile solid state reaction method. The products were characterized by X-ray diffraction(XRD), field emission scanning electron microscopy(FE-SEM) and UV-vis diffuse reflectance spectroscopy(DRS). When BN: BZN=0.1 mole ratio, the BN/BZN composite showed the best visible-light-driven photocatalytic performance, which decomposed nearly 100% of Rh B(10 ppm, p H=3-4) within 40 min. The results demonstrated that in-situ solid state synthesis of BN/BZN composites could be an efficient strategy to develop new photocatalyst for environmental remediation.
基金the National Key Research and Development Program of China(No.2016YFB1100104)the National Natural Science Foundation of China(No.51875470)+1 种基金the State Key Laboratory of Solidification Processing(NPU,China)(2019-QZ-01)the financial support from the fund of SAST(SAST2016043)。
文摘Hot compressive experiments of the laser solid formed(LSFed)TC4 titanium alloy were conducted at a wide temperature range of 650-950℃and strain rate of 0.01-10 s^(-1).The Arrheniustype constitutive models of the LSFed TC4 alloy were established at the temperature range of 800-950℃and of 650-800℃,respectively.The average relative error between the predicted stresses and experimental values in those two temperature ranges are 10.4%and 8.3%,respectively,indicating that the prediction models constructed in this paper are in a good agreement with experimental data.Processing maps were established by the principle of dynamic materials modeling on the basis of the data achieved from the hot compression experiments.The processing parameters corresponding to the stable and unstable regions of material deformation can be determined from the processing maps.The microstructure evolution of the stable and unstable regions of the samples after tests were observed.Finally,the effect of hot compressive parameters on the microstructure were investigated to research the dynamic recrystallization and the texture of the deformed LSFed TC4 alloy.
文摘A novel, high-temperature, mechano-chemical(HTMC) method was developed to synthesise singlephase Sr_2CeO_4:Eu^(3+)phosphor. Phosphors were characterised by X-ray diffraction(XRD), scanning electron microscopy(SEM), and luminescence spectra. Compared with phosphors prepared by the traditional hightemperature solid state method and citric acid gel method, single-phase Sr_2CeO_4:Eu^(3+)powders by using the HTMC method, with small average particle sizes of about 5 μm, a narrow size distribution range and uniform dispersion, were prepared at 800 ℃, and reached their maximum luminescent intensity at 900 ℃.Under ultraviolet excitation at 298 nm, the sample showed good luminescence with the strongest red light of 616 nm. However, Sr_2CeO_4:Eu^(3+)was prepared at the higher temperature of 1100 ℃ by solid state method and citric acid gel method. The particle size was too large and uneven with phosphor agglomeration by high-temperature solid state method. The luminescent intensity reached a maximum for Sr_2CeO_4:Eu^(3+)phosphor at a synthesis temperature of 1100 ℃ by using the high-temperature solid state method, and at 1200 ℃ by both citric acid gel and chemical precipitation methods. Furthermore, the advantages of the Sr_2CeO_4:Eu^(3+)powder prepared by HTMC method were discussed compared with that prepared using traditional high-temperature solid state and citric acid gel methods.