This research focused on developing a modified chemical precipitation(MCP) method for treating wet flue gas desulfurization(FGD) waste water by adding a solid powder reagent directly. Simulated wet FGD wastewater was ...This research focused on developing a modified chemical precipitation(MCP) method for treating wet flue gas desulfurization(FGD) waste water by adding a solid powder reagent directly. Simulated wet FGD wastewater was treated by MCP method in simulation experiments.Optimization experiments were carried out with the help of response surface methodology(RSM) and central composite design(CCD) to evaluate the effects and the interactions of experimental variables, including reagent dosage, temperature and pH value. The optimal reagent dosage, temperature and pH value were 3018.0 mg/L,40.5 °C and 5.7, respectively. The RSM was demonstrated as an appropriate approach for the optimization of wet FGD wastewater treatment with the MCP method. A comparative study between the MCP method and the traditional chemical precipitation(TCP) method on raw wet FGD wastewater treatment was conducted. Results indicate that the MCP had less reagent dosage and variety than the TCP method had. Thus, the MCP method had a lower cost.展开更多
Using cetyltrimethylammonium bromide (CTAB) as the template agent, cerium nitrate as the cerium resource, yttrium nitrate as the yttrium resource, and ammonium carbonate as the precipitating agent, mesoporous CeO2 pow...Using cetyltrimethylammonium bromide (CTAB) as the template agent, cerium nitrate as the cerium resource, yttrium nitrate as the yttrium resource, and ammonium carbonate as the precipitating agent, mesoporous CeO2 powders doped with different yttrium contents were successfully synthesized using a chemical precipitation method, under an alkalescent condition. Properties of the obtained samples were characterized and analyzed with X-ray diffraction (XRD), energy dispersive analysis of X-rays (EDAX), transmission electron microscopy (TEM), infrared (IR) absorbance, and the BET method. For the prepared samples with 20% (molar ratio) Y-doped content, a BET specific surface area of 106.6 m2·g-1, with an average pore size of 3.27 nm were obtained. XRD patterns showed that the doped samples were with a cubic fluorite structure. TEM micrographs revealed that the doped samples showed a spherical morphology with a diameter ranging from 20 to 30 nm and a round pore shape. IR results indicated that the Ce-O-Ce vibration intensity decreased as the Y-doped content increased. N2 adsorption-desorption isotherms showed that the samples possessed typical mesopore characteristics. The average pore size of the samples decreased after mesoporous CeO2 was doped with yttrium, and the average pore size decreased largely as the Y-doped content increased.展开更多
Highly pure active γ-Al2O3 nanoparticles were synthesized from aluminum nitrate and ammonium carbonate with a little surfactant by chemical precipitation method. The factors affecting the synthesis process were studi...Highly pure active γ-Al2O3 nanoparticles were synthesized from aluminum nitrate and ammonium carbonate with a little surfactant by chemical precipitation method. The factors affecting the synthesis process were studied. The properties of γ-Al2O3 nanoparticles were characterized by DTA, XRD, BET, TEM, laser granularity analysis and impurity content analysis. The results show that the amorphous precursor Al（OH）3 sols are produced by using 0.1mol/L Al（NO3）3 ·9H2O and 0.16mol/L （NH4）2CO3·H2O reaction solutions, according to the volume ratio 1.33, adding 0.024% （volume fraction） surfactant PEG600, and reacting at 40℃, 1000r/min stirring rate for 15min. Then, after stabilizing for 24h, the precursors were extracted and filtrated by vacuum, washed thoroughly with deionized water and dehydrated ethanol, dried in vacuum at 80℃ for 8h, final calcined at 800℃ for 1h in the air, and high purity active γ-Al2O3 nanoparticles can be prepared with cubic in crystal system, O7H-FD3M in space group, about 9nm in crystal grain size, about 20nm in particle size and uniform size distribution, 131.35m2/g in BET specific surface area, 711nm in pore diameter, and not lower than 99.93% in purity.展开更多
The uniform layered LiNi1/3Co1/3Mn1/3O2 cathode material for lithium ion batteries was prepared by using (Ni1/3Co1/3Mn1/3)C2O4 as precursor synthesized via oxalate co-precipitation method in air. The effects of calcin...The uniform layered LiNi1/3Co1/3Mn1/3O2 cathode material for lithium ion batteries was prepared by using (Ni1/3Co1/3Mn1/3)C2O4 as precursor synthesized via oxalate co-precipitation method in air. The effects of calcination temperature and time on the structure and electrochemical properties of the LiNi1/3Co1/3Mn1/3O2 were systemically studied. XRD results revealed that the optimal calcination conditions to prepare the layered LiNi1/3Co1/3Mn1/3O2 were 950°C for 15 h. Electrochemical measurement showed that the sample prepared under the such conditions has the highest initial discharge capacity of 160.8 mAh/g and the smallest irreversible capacity loss of 13.5% as well as stable cycling performance at a constant current density of 30 mA/g between 2.5 and 4.3 V versus Li at room temperature.展开更多
The systematic method for constructing Lewis representations is a method for representing chemical bonds between atoms in a molecule. It uses symbols to represent the valence electrons of the atoms involved in the bon...The systematic method for constructing Lewis representations is a method for representing chemical bonds between atoms in a molecule. It uses symbols to represent the valence electrons of the atoms involved in the bond. Using a number of rules in a defined order, it is often better suited to complicated cases than the Lewis representation of atoms. This method allows us to determine the formal charge and oxidation number of each atom in the edifice more efficiently than other methods.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
The exotic species Spartina alterniflora(S.alterniflora)seriously threatens the stability and functioning of saltmarsh ecosystems in the Yangtze Estuary.Ambitious efforts have been undertaken to control this species,b...The exotic species Spartina alterniflora(S.alterniflora)seriously threatens the stability and functioning of saltmarsh ecosystems in the Yangtze Estuary.Ambitious efforts have been undertaken to control this species,but subsequent re-invasion is frequent,presenting a significant barrier to restoration.The complexity and high cost of integrated physical control programs has necessitated a shift in focus,leading to considerable attention being paid to the potential of herbicides to control S.alterniflora.To find a strategy for emergency control of small and scattered patches of re-invading S.alterniflora,an in situ field experiment using Gallant(Haloxyfop-R-methyl)herbicide was conducted.The growth parameters of plant density and height were used to evaluate the control efficiency of different treatment dosages and times and sediment samples were taken for environmental toxicity analysis.The results show the following:(1)the control efficacy of the maximum proposed application dose(2.70 g/m2)was 92%for continuous swards and 100%for small patches,while those of other dosages(0.45 g/m2,0.90 g/m2,and 1.35 g/m2)were lower than 40%;(2)the appropriate implementation time was July to August with 100%mortality resulting from a single application,while S.alterniflora was shown to be capable of recovering rapidly after treatment in May;and(3)there were no significant differences in the community structure of meiofauna among the herbicide treatments and the control,and no herbicide residues were detected in sediment samples collected from treatment areas.This chemical control method was implemented in the Shanghai Chongming Dongtan National Bird Nature Reserve(CDNR).The results of this study indicate that Gallant is an environmentally friendly herbicide with high efficiency,which can be adopted for emergency control of re-invading S.alterniflora.展开更多
Nanocrystalline Gd3Ga5O12:Eu3+ with cubic phase was prepared by a urea homogeneous precipitation method. X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), Fourier transform infrared spectrosc...Nanocrystalline Gd3Ga5O12:Eu3+ with cubic phase was prepared by a urea homogeneous precipitation method. X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric and differential thermal analysis (TG-DTA) and photoluminescence spectra were used to characterize the samples. The effects of the initial solution pH value and urea content on the structure of the sample were studied. The XRD results show that pure phase Gd3Ga5O12 can be obtained at pH =6 and pH =8 of the initial solution. The average crystallite size can be calculated as in the range of 24~33 nm. The average crystallite size decreases with increasing molar ratio of urea to metal ion. The results of excitation spectra and emission spectra show that the emission peaks are ascribed to 5D0→7FJ transitions of Eu3+, and the magnetic dipole transition originated from 5D0 →7F1 of Eu3+ is the strongest; the broad excitation bands belong to change transfer band of Eu?O and the host absorption of Gd3Ga5O12. An efficient energy transfer occurs from Gd3+ to Eu3+.展开更多
We used a chemical reduction method to synthesize the catalysts of cobalt(Co) and cobalt-ruthenium(Co-Ru) bifunctional supported on carbon nanotubes(CNTs) for Fischer–Tropsch synthesis(FTS) in a fixedbed reactor. The...We used a chemical reduction method to synthesize the catalysts of cobalt(Co) and cobalt-ruthenium(Co-Ru) bifunctional supported on carbon nanotubes(CNTs) for Fischer–Tropsch synthesis(FTS) in a fixedbed reactor. These Co-Ru/CNTs catalysts were synthesized with various weight proportions of Ru/Co(0.1 to 0.4 wt%) with keeping a fixed amount of cobalt(10 wt%). Moreover, for comparison purpose, CNTs supported Co-and Co(Ru)-based catalysts at same loading as the above catalysts were prepared through impregnation method. We characterize the present catalysts through the various techniques such as Energy–dispersive X-ray(EDX), Transmission Electron Microscopy(TEM), Brunauer–Emmett–Teller(BET),Hydrogen-Temperature-Programmed Reduction(H_2-TPR), Hydrogen-Temperature-Programmed Desorption(H_2-TPD) and O_2 titration. Thus using the chemical reduction method, a narrow particle size distribution was obtained so that the small cobalt particles were confined inside the CNTs. The Co-based catalyst prepared by impregnation was compared with the Co-Ru catalysts at the same loading. The results demonstrated that the use of chemical reduction method led to decrease the average Co oxide cluster size to8.7 nm so that the reduction enhanced about 24% and stabilized an earlier time at the stream. Among the prepared catalysts, the results indicated that the Co-Ru/CNTs catalysts demonstrated high catalytic activity with the highest long-chain hydrocarbons(C_(5+)), selectivity up to 74.76%, which was higher than those we obtained by the Co-Ru/γ-Al_2O_3(61._20%), Co/CNTs(43.68%) and Co/γ-Al_2O_3(37.69%). At the same time, comparing with those catalyst synthesized by impregnation, the use of chemical reduction led to enhancement of the C_(5+) selectivity from 59.30% to 68.83% and increment in FTS rate about 11% for the Co-Ru/CNTs catalyst.展开更多
A modified wet chemical route for low-temperature synthesis of the calcium stannate CaSnO3, a potentialmaterial for dielectric applications is reported. Firstly, a precursor CaSn(OH)6 was prepared using tin tetrachlor...A modified wet chemical route for low-temperature synthesis of the calcium stannate CaSnO3, a potentialmaterial for dielectric applications is reported. Firstly, a precursor CaSn(OH)6 was prepared using tin tetrachloride,calcium chloride and sodium hydroxide at room temperature. Then the precursor was annealed at relatively low tem-perature of 600 ℃ to obtain CaSnO3. The phase identification, thermal behavior and surface morphology of the sam-ples were characterized by element analysis, X-ray diffraction (XRD), thermo-gravimetric (TG) analysis and deriva-tive thermo-gravimetric (DTG) analysis, Fourier transform infrared spectroscopy (FTIR) and scanning electron mi-croscopy (SEM) in detail. The results show that CaSnO3 obtained by this method possesses a cubic perovskitestructure with average grain size of 5 μm.展开更多
In this paper,the application of an algorithm for precipitation retrieval based on Himawari-8 (H8) satellite infrared data is studied.Based on GPM precipitation data and H8 Infrared spectrum channel brightness tempera...In this paper,the application of an algorithm for precipitation retrieval based on Himawari-8 (H8) satellite infrared data is studied.Based on GPM precipitation data and H8 Infrared spectrum channel brightness temperature data,corresponding "precipitation field dictionary" and "channel brightness temperature dictionary" are formed.The retrieval of precipitation field based on brightness temperature data is studied through the classification rule of k-nearest neighbor domain (KNN) and regularization constraint.Firstly,the corresponding "dictionary" is constructed according to the training sample database of the matched GPM precipitation data and H8 brightness temperature data.Secondly,according to the fact that precipitation characteristics in small organizations in different storm environments are often repeated,KNN is used to identify the spectral brightness temperature signal of "precipitation" and "non-precipitation" based on "the dictionary".Finally,the precipitation field retrieval is carried out in the precipitation signal "subspace" based on the regular term constraint method.In the process of retrieval,the contribution rate of brightness temperature retrieval of different channels was determined by Bayesian model averaging (BMA) model.The preliminary experimental results based on the "quantitative" evaluation indexes show that the precipitation of H8 retrieval has a good correlation with the GPM truth value,with a small error and similar structure.展开更多
CeO 2 nanocrystalline particulates with different sizes were prepared by precipitation method using ethanol as dispersive and protective reagent. XRD spectra show that the synthesized CeO 2 has cubic crystalline struc...CeO 2 nanocrystalline particulates with different sizes were prepared by precipitation method using ethanol as dispersive and protective reagent. XRD spectra show that the synthesized CeO 2 has cubic crystalline structure of space group O 5 H-F M3M, when calcination temperature is in the range of 250～800 ℃. TEM images reveal that CeO 2 particles are spherical in shape. The average size of the particles increases with the increase of calcination temperature. Thermogravimetric analysis indicates that the weight loss of precursor mainly depends on the calcination temperature, and little depends on the calcination time. Measurements of CeO 2 relative density show that the relative density of CeO 2 nanocrystalline powders increases with increasing CeO 2 particle size.展开更多
Zinc sulfide photocatalysts doped with chromium (1:1)% were synthesized via precipitation technique. Their characteristics were studied by X-ray diffraction (XRD), AFM and Florescence spectrometer. The photocatalytic ...Zinc sulfide photocatalysts doped with chromium (1:1)% were synthesized via precipitation technique. Their characteristics were studied by X-ray diffraction (XRD), AFM and Florescence spectrometer. The photocatalytic reaction was applied under light intensity equal to 1.45 × 10-7 Einstein mol-1 to investigate the kinetics and thermodynamic parameters for photo-decolorization of reactive black 5 dye in collide solution of bare and Cr-doped ZnS. The mean crystal size and particle size for bare ZnS are more than those values for prepared Cr loaded ZnS.展开更多
The micron-sized Sr 2(P2O7):Ce,Tb green phosphors were prepared by being annealed at different temperatures with its precursors synthesized by co-precipitates of(NH4) 2HPO4 at ambient temperature. The phase structure,...The micron-sized Sr 2(P2O7):Ce,Tb green phosphors were prepared by being annealed at different temperatures with its precursors synthesized by co-precipitates of(NH4) 2HPO4 at ambient temperature. The phase structure, grain size, surface morphology, and luminescent properties of phosphors were investigated by X-ray diffraction, scanning electron microscope, transmission electron microscope, and fluorescence spectrum. The results show that the product of precursor annealed at 1,100 °C is Sr 2(P 2O7):Ce,Tb, which belongs to orthorhombic phase. The powder is spherical and the size distribution is in micron grade. The sample with the molar ratio of Sr/Tb/Ce of 100.0:0.4:0.6 shows the best fluorescence effect annealed at 1,100 °C for 3 h. The phosphors produce green fluorescence by being excitated with ultraviolet radiation of 254 nm wavelength, and the main emission peak is at 547 nm. The Sr 2(P2O7):Ce,Tb phosphors synthesized by co-precipitation method of precursors at ambient temperature is a kind of efficient green-emitting phosphors.展开更多
The fine powders of Mn-Zn ferrites with uniform size were prepared via chemical coprecipitation method. X-ray diffraction analysis(XRD), scanning electron microscopy(SEM), vibrating sample magnetometer(VSM), frequency...The fine powders of Mn-Zn ferrites with uniform size were prepared via chemical coprecipitation method. X-ray diffraction analysis(XRD), scanning electron microscopy(SEM), vibrating sample magnetometer(VSM), frequency dependence of permeability and metallographical microscope were used to investigate the crystal structure, surface topography and magnetic properties of the powders and the sintering samples. The experimental results demonstrate that the precursor powders have formed a pure phase cubic spinel MnxZn1-xFe2O4 while in the reactor and show definite magnetism, which can solve the difficult issue in washing process effectively. When calcined beneath 450 ℃, the powders have intact crystal form and the crystallite size is less than 20 nm. Comparison tests of sintering temperatures show that 1 300 ℃ is the ideal sintering temperature for Mn-Zn ferrites prepared by using the chemical co-precipitation.展开更多
Water soluble core has been widely used in manufacturing complex metal components with hollow configurations or internal channels;however,the soluble core can absorb water easily from the air at room temperature.To im...Water soluble core has been widely used in manufacturing complex metal components with hollow configurations or internal channels;however,the soluble core can absorb water easily from the air at room temperature.To improve the humidity resistance of the water soluble core and optimize the process parameters applied in manufacturing of the water soluble core,a precipitation method and a two-level-three-full factorial central composite design were used,respectively.The properties of the cores treated by the precipitation method were compared with that without any treatment.Through a systematical study by means of both an environmental scanning electron microscope(ESEM) and an energy dispersive X-ray(EDX) analyzer,the results indicate that the hygroscopicity can be reduced by 20% and the obtained optimal process conditions for three critical control factors affecting the hygroscopicity are 0.2 g·mL-1 calcium chloride concentration,4% water concentration and 0 min ignition time.The porous surface coated by calcium chloride and the high humidity resistance products generated in the precipitation reaction between calcium chloride and potassium carbonate may contribute to the lower hygroscopicity.展开更多
A series of rare earth hydroxide and oxide nanoparticles have been prepared by precipitation method with alcohol as the dispersive and protective reagent. Transmission electron microscope (TEM) images indicate that th...A series of rare earth hydroxide and oxide nanoparticles have been prepared by precipitation method with alcohol as the dispersive and protective reagent. Transmission electron microscope (TEM) images indicate that the particles are spherical in shape and smaller than 100 nm in size. The crystallite sizes of cubic Ln2O3 have lanthanide shrinking effect, while average crystal lattice distortion rates possess lanthanide swelling effect. The diffraction peak intensity of heavy rare earth oxide nanometer powders is remarkably stronger than that of light rare earth oxide nanometer powders. The variation of diffraction intensity with atomic number presents an inverted W type, forming a double peak structure. Fourier transform infrared (FTIR) spectrums reveal that Ln2O3 nanopowders have higher surface activity than that of ordinary Ln2O3 powders. The UV-vis spectra show that Ln-O bond of these particles is slightly blue-shifted, and its absorption intensity decreases.展开更多
Y2O3: Er3+, Yb3+ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm l...Y2O3: Er3+, Yb3+ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3:Er3+,Yb3+ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to 2H11/ 2,4S3/ 2→4I15/ 2 and 4F9/ 2→4I15/2 transitions of the Er3+ ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.展开更多
The influence of chemical composition and cold deformation on aging precipitation behavior of 18Cr-16Mn-2Mo-1.1N(HNS-A), 18Cr-16Mn-1.3N(HNS-B), 18Cr-18Mn-2Mo-0.96N(HNS-C) and 18Cr-18Mn-2Mo-0.77N(HNS-D) high nitrogen a...The influence of chemical composition and cold deformation on aging precipitation behavior of 18Cr-16Mn-2Mo-1.1N(HNS-A), 18Cr-16Mn-1.3N(HNS-B), 18Cr-18Mn-2Mo-0.96N(HNS-C) and 18Cr-18Mn-2Mo-0.77N(HNS-D) high nitrogen austenitic stainless steels was investigated. The results show that the "nose" temperatures and incubation periods of the initial time temperature precipitation(TTP) curves of aged HNSs are found to be 850℃,60s; 850℃, 45s; 850℃, 60 s and 900℃,90s, respectively. Based on the analysis of SAD patterns, the coarse cellular Cr2N precipitate which presents a lamellar structure has a hexagonal structure of a=0.478 nm and c=0.444 nm. The χ phase corresponding to a composition of Fe36Cr12Mo10, is determined to be a body-centered cubic structure of a=0.892 nm. The precipitating sensitivity presents no more difference with the nitrogen content increasing from 0.77% to 0.96%, but exhibits so obviously that the cellular precipitates nearly overspread the whole field. The addition of Mo element can restrain the TTP curves moving left and down, which means decreasing the sensitivity of aging precipitation. With increasing the cold deformation, the sensitivity of precipitation increases obviously.展开更多
文摘This research focused on developing a modified chemical precipitation(MCP) method for treating wet flue gas desulfurization(FGD) waste water by adding a solid powder reagent directly. Simulated wet FGD wastewater was treated by MCP method in simulation experiments.Optimization experiments were carried out with the help of response surface methodology(RSM) and central composite design(CCD) to evaluate the effects and the interactions of experimental variables, including reagent dosage, temperature and pH value. The optimal reagent dosage, temperature and pH value were 3018.0 mg/L,40.5 °C and 5.7, respectively. The RSM was demonstrated as an appropriate approach for the optimization of wet FGD wastewater treatment with the MCP method. A comparative study between the MCP method and the traditional chemical precipitation(TCP) method on raw wet FGD wastewater treatment was conducted. Results indicate that the MCP had less reagent dosage and variety than the TCP method had. Thus, the MCP method had a lower cost.
基金Project supported by the International Cooperation of Science and Technology Ministry PRC (2005DFBA028)the National Natural Science Foundation of China (59925412)
文摘Using cetyltrimethylammonium bromide (CTAB) as the template agent, cerium nitrate as the cerium resource, yttrium nitrate as the yttrium resource, and ammonium carbonate as the precipitating agent, mesoporous CeO2 powders doped with different yttrium contents were successfully synthesized using a chemical precipitation method, under an alkalescent condition. Properties of the obtained samples were characterized and analyzed with X-ray diffraction (XRD), energy dispersive analysis of X-rays (EDAX), transmission electron microscopy (TEM), infrared (IR) absorbance, and the BET method. For the prepared samples with 20% (molar ratio) Y-doped content, a BET specific surface area of 106.6 m2·g-1, with an average pore size of 3.27 nm were obtained. XRD patterns showed that the doped samples were with a cubic fluorite structure. TEM micrographs revealed that the doped samples showed a spherical morphology with a diameter ranging from 20 to 30 nm and a round pore shape. IR results indicated that the Ce-O-Ce vibration intensity decreased as the Y-doped content increased. N2 adsorption-desorption isotherms showed that the samples possessed typical mesopore characteristics. The average pore size of the samples decreased after mesoporous CeO2 was doped with yttrium, and the average pore size decreased largely as the Y-doped content increased.
文摘Highly pure active γ-Al2O3 nanoparticles were synthesized from aluminum nitrate and ammonium carbonate with a little surfactant by chemical precipitation method. The factors affecting the synthesis process were studied. The properties of γ-Al2O3 nanoparticles were characterized by DTA, XRD, BET, TEM, laser granularity analysis and impurity content analysis. The results show that the amorphous precursor Al（OH）3 sols are produced by using 0.1mol/L Al（NO3）3 ·9H2O and 0.16mol/L （NH4）2CO3·H2O reaction solutions, according to the volume ratio 1.33, adding 0.024% （volume fraction） surfactant PEG600, and reacting at 40℃, 1000r/min stirring rate for 15min. Then, after stabilizing for 24h, the precursors were extracted and filtrated by vacuum, washed thoroughly with deionized water and dehydrated ethanol, dried in vacuum at 80℃ for 8h, final calcined at 800℃ for 1h in the air, and high purity active γ-Al2O3 nanoparticles can be prepared with cubic in crystal system, O7H-FD3M in space group, about 9nm in crystal grain size, about 20nm in particle size and uniform size distribution, 131.35m2/g in BET specific surface area, 711nm in pore diameter, and not lower than 99.93% in purity.
基金financially supported by the Natural Science Foundation of Guangxi Province, China (No. GKZ0832256)
文摘The uniform layered LiNi1/3Co1/3Mn1/3O2 cathode material for lithium ion batteries was prepared by using (Ni1/3Co1/3Mn1/3)C2O4 as precursor synthesized via oxalate co-precipitation method in air. The effects of calcination temperature and time on the structure and electrochemical properties of the LiNi1/3Co1/3Mn1/3O2 were systemically studied. XRD results revealed that the optimal calcination conditions to prepare the layered LiNi1/3Co1/3Mn1/3O2 were 950°C for 15 h. Electrochemical measurement showed that the sample prepared under the such conditions has the highest initial discharge capacity of 160.8 mAh/g and the smallest irreversible capacity loss of 13.5% as well as stable cycling performance at a constant current density of 30 mA/g between 2.5 and 4.3 V versus Li at room temperature.
文摘The systematic method for constructing Lewis representations is a method for representing chemical bonds between atoms in a molecule. It uses symbols to represent the valence electrons of the atoms involved in the bond. Using a number of rules in a defined order, it is often better suited to complicated cases than the Lewis representation of atoms. This method allows us to determine the formal charge and oxidation number of each atom in the edifice more efficiently than other methods.
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supported by the National Key Research and Development Program of China(Grant No.2016YFC1201100)the National Natural Science Foundation of China(Grant No.41876093)the Scientific Research Project of the Shanghai Science and Technology Committee(Grants No.17DZ1201902,18DZ1206506,and 18DZ1204802).
文摘The exotic species Spartina alterniflora(S.alterniflora)seriously threatens the stability and functioning of saltmarsh ecosystems in the Yangtze Estuary.Ambitious efforts have been undertaken to control this species,but subsequent re-invasion is frequent,presenting a significant barrier to restoration.The complexity and high cost of integrated physical control programs has necessitated a shift in focus,leading to considerable attention being paid to the potential of herbicides to control S.alterniflora.To find a strategy for emergency control of small and scattered patches of re-invading S.alterniflora,an in situ field experiment using Gallant(Haloxyfop-R-methyl)herbicide was conducted.The growth parameters of plant density and height were used to evaluate the control efficiency of different treatment dosages and times and sediment samples were taken for environmental toxicity analysis.The results show the following:(1)the control efficacy of the maximum proposed application dose(2.70 g/m2)was 92%for continuous swards and 100%for small patches,while those of other dosages(0.45 g/m2,0.90 g/m2,and 1.35 g/m2)were lower than 40%;(2)the appropriate implementation time was July to August with 100%mortality resulting from a single application,while S.alterniflora was shown to be capable of recovering rapidly after treatment in May;and(3)there were no significant differences in the community structure of meiofauna among the herbicide treatments and the control,and no herbicide residues were detected in sediment samples collected from treatment areas.This chemical control method was implemented in the Shanghai Chongming Dongtan National Bird Nature Reserve(CDNR).The results of this study indicate that Gallant is an environmentally friendly herbicide with high efficiency,which can be adopted for emergency control of re-invading S.alterniflora.
基金financially supported by the Science and Technology Research Project of Department of Education of Liaoning Province,China(No.L2011063)
文摘Nanocrystalline Gd3Ga5O12:Eu3+ with cubic phase was prepared by a urea homogeneous precipitation method. X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric and differential thermal analysis (TG-DTA) and photoluminescence spectra were used to characterize the samples. The effects of the initial solution pH value and urea content on the structure of the sample were studied. The XRD results show that pure phase Gd3Ga5O12 can be obtained at pH =6 and pH =8 of the initial solution. The average crystallite size can be calculated as in the range of 24~33 nm. The average crystallite size decreases with increasing molar ratio of urea to metal ion. The results of excitation spectra and emission spectra show that the emission peaks are ascribed to 5D0→7FJ transitions of Eu3+, and the magnetic dipole transition originated from 5D0 →7F1 of Eu3+ is the strongest; the broad excitation bands belong to change transfer band of Eu?O and the host absorption of Gd3Ga5O12. An efficient energy transfer occurs from Gd3+ to Eu3+.
文摘We used a chemical reduction method to synthesize the catalysts of cobalt(Co) and cobalt-ruthenium(Co-Ru) bifunctional supported on carbon nanotubes(CNTs) for Fischer–Tropsch synthesis(FTS) in a fixedbed reactor. These Co-Ru/CNTs catalysts were synthesized with various weight proportions of Ru/Co(0.1 to 0.4 wt%) with keeping a fixed amount of cobalt(10 wt%). Moreover, for comparison purpose, CNTs supported Co-and Co(Ru)-based catalysts at same loading as the above catalysts were prepared through impregnation method. We characterize the present catalysts through the various techniques such as Energy–dispersive X-ray(EDX), Transmission Electron Microscopy(TEM), Brunauer–Emmett–Teller(BET),Hydrogen-Temperature-Programmed Reduction(H_2-TPR), Hydrogen-Temperature-Programmed Desorption(H_2-TPD) and O_2 titration. Thus using the chemical reduction method, a narrow particle size distribution was obtained so that the small cobalt particles were confined inside the CNTs. The Co-based catalyst prepared by impregnation was compared with the Co-Ru catalysts at the same loading. The results demonstrated that the use of chemical reduction method led to decrease the average Co oxide cluster size to8.7 nm so that the reduction enhanced about 24% and stabilized an earlier time at the stream. Among the prepared catalysts, the results indicated that the Co-Ru/CNTs catalysts demonstrated high catalytic activity with the highest long-chain hydrocarbons(C_(5+)), selectivity up to 74.76%, which was higher than those we obtained by the Co-Ru/γ-Al_2O_3(61._20%), Co/CNTs(43.68%) and Co/γ-Al_2O_3(37.69%). At the same time, comparing with those catalyst synthesized by impregnation, the use of chemical reduction led to enhancement of the C_(5+) selectivity from 59.30% to 68.83% and increment in FTS rate about 11% for the Co-Ru/CNTs catalyst.
文摘A modified wet chemical route for low-temperature synthesis of the calcium stannate CaSnO3, a potentialmaterial for dielectric applications is reported. Firstly, a precursor CaSn(OH)6 was prepared using tin tetrachloride,calcium chloride and sodium hydroxide at room temperature. Then the precursor was annealed at relatively low tem-perature of 600 ℃ to obtain CaSnO3. The phase identification, thermal behavior and surface morphology of the sam-ples were characterized by element analysis, X-ray diffraction (XRD), thermo-gravimetric (TG) analysis and deriva-tive thermo-gravimetric (DTG) analysis, Fourier transform infrared spectroscopy (FTIR) and scanning electron mi-croscopy (SEM) in detail. The results show that CaSnO3 obtained by this method possesses a cubic perovskitestructure with average grain size of 5 μm.
基金Supported by National Natural Science Foundation of China(41805080)Natural Science Foundation of Anhui Province,China(1708085QD89)+1 种基金Key Research and Development Program Projects of Anhui Province,China(201904a07020099)Open Foundation Project Shenyang Institute of Atmospheric Environment,China Meteorological Administration(2016SYIAE14)
文摘In this paper,the application of an algorithm for precipitation retrieval based on Himawari-8 (H8) satellite infrared data is studied.Based on GPM precipitation data and H8 Infrared spectrum channel brightness temperature data,corresponding "precipitation field dictionary" and "channel brightness temperature dictionary" are formed.The retrieval of precipitation field based on brightness temperature data is studied through the classification rule of k-nearest neighbor domain (KNN) and regularization constraint.Firstly,the corresponding "dictionary" is constructed according to the training sample database of the matched GPM precipitation data and H8 brightness temperature data.Secondly,according to the fact that precipitation characteristics in small organizations in different storm environments are often repeated,KNN is used to identify the spectral brightness temperature signal of "precipitation" and "non-precipitation" based on "the dictionary".Finally,the precipitation field retrieval is carried out in the precipitation signal "subspace" based on the regular term constraint method.In the process of retrieval,the contribution rate of brightness temperature retrieval of different channels was determined by Bayesian model averaging (BMA) model.The preliminary experimental results based on the "quantitative" evaluation indexes show that the precipitation of H8 retrieval has a good correlation with the GPM truth value,with a small error and similar structure.
文摘CeO 2 nanocrystalline particulates with different sizes were prepared by precipitation method using ethanol as dispersive and protective reagent. XRD spectra show that the synthesized CeO 2 has cubic crystalline structure of space group O 5 H-F M3M, when calcination temperature is in the range of 250～800 ℃. TEM images reveal that CeO 2 particles are spherical in shape. The average size of the particles increases with the increase of calcination temperature. Thermogravimetric analysis indicates that the weight loss of precursor mainly depends on the calcination temperature, and little depends on the calcination time. Measurements of CeO 2 relative density show that the relative density of CeO 2 nanocrystalline powders increases with increasing CeO 2 particle size.
文摘Zinc sulfide photocatalysts doped with chromium (1:1)% were synthesized via precipitation technique. Their characteristics were studied by X-ray diffraction (XRD), AFM and Florescence spectrometer. The photocatalytic reaction was applied under light intensity equal to 1.45 × 10-7 Einstein mol-1 to investigate the kinetics and thermodynamic parameters for photo-decolorization of reactive black 5 dye in collide solution of bare and Cr-doped ZnS. The mean crystal size and particle size for bare ZnS are more than those values for prepared Cr loaded ZnS.
基金financially supported by the National Natural Science Foundation of China(No.21273060)the Program for New Century Excellent Talents in Heilongjiang Provincial University(No.1251-NCET-014)
文摘The micron-sized Sr 2(P2O7):Ce,Tb green phosphors were prepared by being annealed at different temperatures with its precursors synthesized by co-precipitates of(NH4) 2HPO4 at ambient temperature. The phase structure, grain size, surface morphology, and luminescent properties of phosphors were investigated by X-ray diffraction, scanning electron microscope, transmission electron microscope, and fluorescence spectrum. The results show that the product of precursor annealed at 1,100 °C is Sr 2(P 2O7):Ce,Tb, which belongs to orthorhombic phase. The powder is spherical and the size distribution is in micron grade. The sample with the molar ratio of Sr/Tb/Ce of 100.0:0.4:0.6 shows the best fluorescence effect annealed at 1,100 °C for 3 h. The phosphors produce green fluorescence by being excitated with ultraviolet radiation of 254 nm wavelength, and the main emission peak is at 547 nm. The Sr 2(P2O7):Ce,Tb phosphors synthesized by co-precipitation method of precursors at ambient temperature is a kind of efficient green-emitting phosphors.
基金Funded by the National Natural Science Foundation of China(Nos.51162019 and 51462019)
文摘The fine powders of Mn-Zn ferrites with uniform size were prepared via chemical coprecipitation method. X-ray diffraction analysis(XRD), scanning electron microscopy(SEM), vibrating sample magnetometer(VSM), frequency dependence of permeability and metallographical microscope were used to investigate the crystal structure, surface topography and magnetic properties of the powders and the sintering samples. The experimental results demonstrate that the precursor powders have formed a pure phase cubic spinel MnxZn1-xFe2O4 while in the reactor and show definite magnetism, which can solve the difficult issue in washing process effectively. When calcined beneath 450 ℃, the powders have intact crystal form and the crystallite size is less than 20 nm. Comparison tests of sintering temperatures show that 1 300 ℃ is the ideal sintering temperature for Mn-Zn ferrites prepared by using the chemical co-precipitation.
文摘Water soluble core has been widely used in manufacturing complex metal components with hollow configurations or internal channels;however,the soluble core can absorb water easily from the air at room temperature.To improve the humidity resistance of the water soluble core and optimize the process parameters applied in manufacturing of the water soluble core,a precipitation method and a two-level-three-full factorial central composite design were used,respectively.The properties of the cores treated by the precipitation method were compared with that without any treatment.Through a systematical study by means of both an environmental scanning electron microscope(ESEM) and an energy dispersive X-ray(EDX) analyzer,the results indicate that the hygroscopicity can be reduced by 20% and the obtained optimal process conditions for three critical control factors affecting the hygroscopicity are 0.2 g·mL-1 calcium chloride concentration,4% water concentration and 0 min ignition time.The porous surface coated by calcium chloride and the high humidity resistance products generated in the precipitation reaction between calcium chloride and potassium carbonate may contribute to the lower hygroscopicity.
文摘A series of rare earth hydroxide and oxide nanoparticles have been prepared by precipitation method with alcohol as the dispersive and protective reagent. Transmission electron microscope (TEM) images indicate that the particles are spherical in shape and smaller than 100 nm in size. The crystallite sizes of cubic Ln2O3 have lanthanide shrinking effect, while average crystal lattice distortion rates possess lanthanide swelling effect. The diffraction peak intensity of heavy rare earth oxide nanometer powders is remarkably stronger than that of light rare earth oxide nanometer powders. The variation of diffraction intensity with atomic number presents an inverted W type, forming a double peak structure. Fourier transform infrared (FTIR) spectrums reveal that Ln2O3 nanopowders have higher surface activity than that of ordinary Ln2O3 powders. The UV-vis spectra show that Ln-O bond of these particles is slightly blue-shifted, and its absorption intensity decreases.
基金the Foundation for the University by Educational Department of Liaoning (05L337)Key Laboratory of Rare Earth Chemistry and Physics, Chinese Academy of Sciences
文摘Y2O3: Er3+, Yb3+ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3:Er3+,Yb3+ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to 2H11/ 2,4S3/ 2→4I15/ 2 and 4F9/ 2→4I15/2 transitions of the Er3+ ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.
基金Project(51304041) supported by the National Natural Science Foundation of ChinaProject(N100402015) supported by Fundamental Research Funds for the Central Universities of China+1 种基金Project(2012AA03A502) supported by the National High Technology Research and Development Program of ChinaProject supported by Program for Liaoning Innovative Research Team in University,China
文摘The influence of chemical composition and cold deformation on aging precipitation behavior of 18Cr-16Mn-2Mo-1.1N(HNS-A), 18Cr-16Mn-1.3N(HNS-B), 18Cr-18Mn-2Mo-0.96N(HNS-C) and 18Cr-18Mn-2Mo-0.77N(HNS-D) high nitrogen austenitic stainless steels was investigated. The results show that the "nose" temperatures and incubation periods of the initial time temperature precipitation(TTP) curves of aged HNSs are found to be 850℃,60s; 850℃, 45s; 850℃, 60 s and 900℃,90s, respectively. Based on the analysis of SAD patterns, the coarse cellular Cr2N precipitate which presents a lamellar structure has a hexagonal structure of a=0.478 nm and c=0.444 nm. The χ phase corresponding to a composition of Fe36Cr12Mo10, is determined to be a body-centered cubic structure of a=0.892 nm. The precipitating sensitivity presents no more difference with the nitrogen content increasing from 0.77% to 0.96%, but exhibits so obviously that the cellular precipitates nearly overspread the whole field. The addition of Mo element can restrain the TTP curves moving left and down, which means decreasing the sensitivity of aging precipitation. With increasing the cold deformation, the sensitivity of precipitation increases obviously.
