Nanometer α-Fe2O3 catalysts were prepared by hydrolyzation in high temperature. Three kinds of precipitators, NaOH, （NH4）2CO3 and urea were used to compare the effect in the process of hydrolyzation. Nanometer size...Nanometer α-Fe2O3 catalysts were prepared by hydrolyzation in high temperature. Three kinds of precipitators, NaOH, （NH4）2CO3 and urea were used to compare the effect in the process of hydrolyzation. Nanometer sizer, transmission electron microscopy （TEM） and X-ray diffraction （XRD） were employed to test the profiles and diameters of the product particles. The test results indicate that the production is nanometer α-Fe2O3 with narrow particle size distribution （PSD） and good dispersibility. The catalysts are mixed with ammonia perchlorate （AP） in 1.0 wt.%. And the composite particles of catalysts with AP are prepared using a new solvent-nonsolvent method. Differential thermal analyzer （DTA） is employed to analysis the thermal decomposition of the composite particles and pure AP sample. The results imply that the thermal decomposition curve peaks of the samples in which nanometer α-Fe2O3 catalysts are added appear comparatively more ahead than that of pure AP sample. Among these mixtures added nanometer material, the smaller the particle diameter of catalyst is, the more ahead the thermal decomposition curve peaks of AP appear. The high and low temperature thermal decomposition curve peaks of AP mixed with the catalyst deposed by urea are more ahead of 77.8?℃ and 9.7?℃ than that of pure AP, respectively. The mechanism of the catalyst deposed by urea with smaller diameter and the distinct catalysis of the particles on the thermal decomposition of AP are discussed.展开更多
The preparation of nanometer γ-Fe2O3 through an electrochemical process was studied at room temperature, using a metal iron plate as sacrificing anode and a sheet of stainless steel as cathode, in non-aqueous mediate...The preparation of nanometer γ-Fe2O3 through an electrochemical process was studied at room temperature, using a metal iron plate as sacrificing anode and a sheet of stainless steel as cathode, in non-aqueous mediate containing （Bu）4 NBr as support electrolyre and 2% （vol%） water. The powdery particles obtained were then calcined at 300 ℃. The products were characterized by IR, XRD, SEM, TEM and laser particle size analyser, indicating the fine particle is a pure nanometer γ-Fe2O3. The morphology is like coneshaped and their average size is 22.0 nm. Furthermore the VSM spectrum shows that the particle＇s coercivity （3.9 × 10^3 A/m） is rather small, presenting the excellent super-paramagnetism.展开更多
Ammonium aluminum carbonate hydroxide (AACH) precursor was synthesized by the precipitation reaction of aluminum sulfate and ammonium carbonate. Then the precursor was dealt with five drying methods including ordinary...Ammonium aluminum carbonate hydroxide (AACH) precursor was synthesized by the precipitation reaction of aluminum sulfate and ammonium carbonate. Then the precursor was dealt with five drying methods including ordinary drying, alcohol exchange, vacuum freeze-drying, glycol distillation, n-butanol azeotropic distillation respectively and calcined at 1 200 ℃ for 2 h to get α-Al2O3. The effects of drying methods on preparation of nanometer α-Al2O3 were discussed, and the optimal drying method was confirmed. The structural properties of powders were characterized by XRD, SEM and BET measurements. The results show that vacuum freeze-drying, glycol distillation and n-butanol azeotropic distillation can prevent the powders from aggregating, and among them the n-butanol azeotropic distillation is the best method. The nanometer α-Al2O3 powder with non-aggregation can be manufactured using n-butanol azeotropic distillation and the average particle size is about 40 nm.展开更多
W-2 wt.%Y2O3 composite material with uniform distribution of yttrium element was fabricated through processes of mechanical alloying （MA） and spark plasma sintering （SPS）. The relevant productions were characteriz...W-2 wt.%Y2O3 composite material with uniform distribution of yttrium element was fabricated through processes of mechanical alloying （MA） and spark plasma sintering （SPS）. The relevant productions were characterized by scanning electron microscopy （SEM）, energy dispersive spectroscopy （EDS）, X-ray diffraction （XRD）, and transmission electron microscopy （TEM）. The XRD showed that the W-2 wt.%Y2O3 composite powder, including tungsten matrix and Y2O3 particles, was refined to nanometer sizes during the MA process. The SEM and TEM micrographs showed that the MA produced composite powder presented a lamellar morphology and contained many dislocations and microcracks. The EDS showed that the Y and O elements were uniformly distributed in the W matrix after mechanically alloying for 15 h. The W-2 wt.%Y2O3 composite material with uniform distribution of yttrium was obtained by sintering of the MA produced composite powder.展开更多
A new nanometer material, nano-Al2O3 with carbon fibre as the carrier, was employed for the removal of Cd with low concentrations from polluted water. The characterization of the material was carried out by means of S...A new nanometer material, nano-Al2O3 with carbon fibre as the carrier, was employed for the removal of Cd with low concentrations from polluted water. The characterization of the material was carried out by means of SEM and TEM. Batch adsorption and elution experiments were carried out to determine the adsorption properties of Cd on the new adsorbent. The classical Thomas model was applied to estimating the equilibrium coefficients of Cd adsorption and the saturated adsorption ability. The results show that the Thomas model is fit for describing the kinetic adsorption process, and the maximum adsorption capacity of the nanometer Al2O3/carbon is 69.29 mg/g. The resulting information also indicates that the desorption of Cd eluted with de-ionized water at a rate of 9.8 mL/min can be neglected. With the advantage of a high adsorption capacity for removing low concentration Cd, the Al2O3/carbon fibre possesses the potentiality to be an effective adsorbent for the removal of Cd from polluted water.展开更多
文摘Nanometer α-Fe2O3 catalysts were prepared by hydrolyzation in high temperature. Three kinds of precipitators, NaOH, （NH4）2CO3 and urea were used to compare the effect in the process of hydrolyzation. Nanometer sizer, transmission electron microscopy （TEM） and X-ray diffraction （XRD） were employed to test the profiles and diameters of the product particles. The test results indicate that the production is nanometer α-Fe2O3 with narrow particle size distribution （PSD） and good dispersibility. The catalysts are mixed with ammonia perchlorate （AP） in 1.0 wt.%. And the composite particles of catalysts with AP are prepared using a new solvent-nonsolvent method. Differential thermal analyzer （DTA） is employed to analysis the thermal decomposition of the composite particles and pure AP sample. The results imply that the thermal decomposition curve peaks of the samples in which nanometer α-Fe2O3 catalysts are added appear comparatively more ahead than that of pure AP sample. Among these mixtures added nanometer material, the smaller the particle diameter of catalyst is, the more ahead the thermal decomposition curve peaks of AP appear. The high and low temperature thermal decomposition curve peaks of AP mixed with the catalyst deposed by urea are more ahead of 77.8?℃ and 9.7?℃ than that of pure AP, respectively. The mechanism of the catalyst deposed by urea with smaller diameter and the distinct catalysis of the particles on the thermal decomposition of AP are discussed.
文摘The preparation of nanometer γ-Fe2O3 through an electrochemical process was studied at room temperature, using a metal iron plate as sacrificing anode and a sheet of stainless steel as cathode, in non-aqueous mediate containing （Bu）4 NBr as support electrolyre and 2% （vol%） water. The powdery particles obtained were then calcined at 300 ℃. The products were characterized by IR, XRD, SEM, TEM and laser particle size analyser, indicating the fine particle is a pure nanometer γ-Fe2O3. The morphology is like coneshaped and their average size is 22.0 nm. Furthermore the VSM spectrum shows that the particle＇s coercivity （3.9 × 10^3 A/m） is rather small, presenting the excellent super-paramagnetism.
基金Project (5JJ30103) supported by the Natural Science Foundation of Hunan Province, China
文摘Ammonium aluminum carbonate hydroxide (AACH) precursor was synthesized by the precipitation reaction of aluminum sulfate and ammonium carbonate. Then the precursor was dealt with five drying methods including ordinary drying, alcohol exchange, vacuum freeze-drying, glycol distillation, n-butanol azeotropic distillation respectively and calcined at 1 200 ℃ for 2 h to get α-Al2O3. The effects of drying methods on preparation of nanometer α-Al2O3 were discussed, and the optimal drying method was confirmed. The structural properties of powders were characterized by XRD, SEM and BET measurements. The results show that vacuum freeze-drying, glycol distillation and n-butanol azeotropic distillation can prevent the powders from aggregating, and among them the n-butanol azeotropic distillation is the best method. The nanometer α-Al2O3 powder with non-aggregation can be manufactured using n-butanol azeotropic distillation and the average particle size is about 40 nm.
文摘W-2 wt.%Y2O3 composite material with uniform distribution of yttrium element was fabricated through processes of mechanical alloying （MA） and spark plasma sintering （SPS）. The relevant productions were characterized by scanning electron microscopy （SEM）, energy dispersive spectroscopy （EDS）, X-ray diffraction （XRD）, and transmission electron microscopy （TEM）. The XRD showed that the W-2 wt.%Y2O3 composite powder, including tungsten matrix and Y2O3 particles, was refined to nanometer sizes during the MA process. The SEM and TEM micrographs showed that the MA produced composite powder presented a lamellar morphology and contained many dislocations and microcracks. The EDS showed that the Y and O elements were uniformly distributed in the W matrix after mechanically alloying for 15 h. The W-2 wt.%Y2O3 composite material with uniform distribution of yttrium was obtained by sintering of the MA produced composite powder.
基金Supported by the Starting Foundation for Graduated Doctors in Jilin University(No.420010302353).
文摘A new nanometer material, nano-Al2O3 with carbon fibre as the carrier, was employed for the removal of Cd with low concentrations from polluted water. The characterization of the material was carried out by means of SEM and TEM. Batch adsorption and elution experiments were carried out to determine the adsorption properties of Cd on the new adsorbent. The classical Thomas model was applied to estimating the equilibrium coefficients of Cd adsorption and the saturated adsorption ability. The results show that the Thomas model is fit for describing the kinetic adsorption process, and the maximum adsorption capacity of the nanometer Al2O3/carbon is 69.29 mg/g. The resulting information also indicates that the desorption of Cd eluted with de-ionized water at a rate of 9.8 mL/min can be neglected. With the advantage of a high adsorption capacity for removing low concentration Cd, the Al2O3/carbon fibre possesses the potentiality to be an effective adsorbent for the removal of Cd from polluted water.
