Muscovite mineral was roasted in different conditions.Rubidium leaching rate was a standard to examine the impact of various factors on calcination effect,including the agent types,roasting time,mass ratio,and roastin...Muscovite mineral was roasted in different conditions.Rubidium leaching rate was a standard to examine the impact of various factors on calcination effect,including the agent types,roasting time,mass ratio,and roasting temperature.The results indicate that the best agent is the combination of sodium chloride and calcium chloride,and its mass ratio of muscovite/NaCl/CaCl2is1.00:0.25:0.25.Calcined at 850℃ for 30 min,the rubidium leaching rate is up to 90.12%.The reaction of muscovite ore with the chlorinating agent CaCl2was studied by TG/DSC,and the surface morphology before and after leaching was characterized by SEM.Rubidium chloride products can be obtained using t-BAMBP extraction,hydrochloric acid re-extraction,and purification.展开更多
Perovskite-type V-doped titanium-bearing blast furnace slag (VTBBFS) photocatalyst was prepared by high-temperature solid phase method.The influence of calcination temperature on the photocatalytic and antibacterial p...Perovskite-type V-doped titanium-bearing blast furnace slag (VTBBFS) photocatalyst was prepared by high-temperature solid phase method.The influence of calcination temperature on the photocatalytic and antibacterial properties of VTBBFS was studied in details.Its composition and microstructure were evaluated by X-ray diffractometer,ultraviolet-visible absorption spectrometer,Fourier transform infrared spectrometer and scanning electron microscope.The antibacterial properties of VTBBFS to Candida albicans were investigated by flask oscillation method.The results showed that the optical absorption and antibacterial properties of VTBBFS were the best with 10%(ω) doping of vanadium,prepared at 800℃ for 2 h,and its sterilization rate was close to 100% to Candida albicans (ATCC10231).The minimum inhibitory and minimum bactericidal concentrations were 25 and 50 mg/mL.When the concentration was 0.2 μg/mL,the catalyst had the least toxic toxicity.展开更多
Pd-doped organosilica membranes were prepared by controlling calcination atmospheres(i.e.POS-Air,POS-N2,POS-H2,POS-H2/N2)to tailor their networks for improving their gas separation performance.This study shows that Pd...Pd-doped organosilica membranes were prepared by controlling calcination atmospheres(i.e.POS-Air,POS-N2,POS-H2,POS-H2/N2)to tailor their networks for improving their gas separation performance.This study shows that Pd(Ⅱ)could be only maintained under non-reductive calcination atmosphere,while inert and reducing calcination atmosphere is more beneficial to maintain organosilica moieties in POS networks.POS-H2/N2 membrane showed the optimal H2 separation performance that its permselectivities for H2/CO2,H2/N2,H2/CH4 and H2/SF6 are 15.0,96.7,173.0 and 3400.0,re spectively.Moreover,it is found that H2 molecules pass through the four membranes based on activated diffusion,while CO2 molecules permeation through POS-N2 and POS-Air membrane is dominated by surface diffusion.This work may provide insight into the understanding of the calcination atmosphere effect on gas separation performance of metal-doped organosilica membranes.展开更多
To enable the utilization of low-grade and high-sulfur bauxite, the suspension calcination was used to remove the sulfur and the activate silica minerals, and the calcinated bauxite was subjected to a desilication pro...To enable the utilization of low-grade and high-sulfur bauxite, the suspension calcination was used to remove the sulfur and the activate silica minerals, and the calcinated bauxite was subjected to a desilication process in Na OH solution under atmospheric pressure. The desulfurization and desilication properties and mineralogical evolution were studied by X-ray diffraction, thermogravimetry–differential thermal analysis, scanning electron microscopy, and FactSage methods. The results demonstrate that the suspension calcination method is efficient for sulfur removal: 84.21% of S was removed after calcination at 1000°C for 2 min. During the calcination process, diaspore and pyrite were transferred to α-Al2O3, magnetite, and hematite. The phase transformation of pyrite follows the order FeS2 → Fe3O4 → Fe2O3, and the iron oxides and silica were converted into iron silicate. In the alkali-soluble desilication process, the optimum condition was an alkali solution concentration of 110 g/L, a reaction time of 20 min, and a reaction temperature of 95°C. The corresponding desilication ratio and alumina loss ratio were 44.9% and 2.4%, respectively, and the alumina-to-silica mass ratio of the concentrate was 7.9. The Al2O3·2SiO2, SiO2, and Al2O3 formed during the calcination process could react with Na OH solution, and their activity decreased in the order of Al2O3·2 SiO2, SiO2, and Al2O3.展开更多
Co_3O_4/CeO_2 composites with high surface areas and ultrafine crystalline sizes for catalytic combustion of methane were firstly prepared by a new sol-gel method which combined ultrasonic impregnation treatment and c...Co_3O_4/CeO_2 composites with high surface areas and ultrafine crystalline sizes for catalytic combustion of methane were firstly prepared by a new sol-gel method which combined ultrasonic impregnation treatment and calcination in N_2 atmosphere. The samples were characterized by various means such as nitrogen adsorption/desorption, X-ray diffraction(XRD), H_2 temperature-programmed reduction(H_2-TPR),X-ray photoelectron spectroscopy(XPS) and transmission electron microscopy(TEM). Results showed that the modified catalyst had the mesoporous structure, comparatively higher amount of surface oxygen and larger oxygen vacancies than others. As a result of the structure and surface composition merits, a high methane combustion conversion(50%) could be obtained at a low temperature of 262 °C for the modified Co_3O_4/CeO_2 composites catalysts. The experimental results demonstrated that ultrasonic impregnation treatment combined with the N_2 thermal treatment prior to calcination in air had a promising application for preparation of Co_3O_4/CeO_2 composites catalysts for low-temperature catalytic combustion of methane.展开更多
Lanthanum-containing(LaX)and cerium-containing X zeolites(CeX)were prepared by a doubleexchange,double-calcination method.By changing the calcination atmospheres between nitrogen and air,the Ce^(IV) contents in CeX ze...Lanthanum-containing(LaX)and cerium-containing X zeolites(CeX)were prepared by a doubleexchange,double-calcination method.By changing the calcination atmospheres between nitrogen and air,the Ce^(IV) contents in CeX zeolites were adjusted and their impacts on physicochemical properties and catalytic performance in isobutane alkylation were established.The crystallinity of CeX zeolite was found to be negatively correlated with the Ce^(IV) content.This i s believed to be due to the water formed during the oxidation of Ce^(III),which facilitates the framework dealumination.As a consequence,calcining in air resulted in a great elimination of strong Brønsted acid sites while under nitrogen protection,this phenomenon was mostly hindered and the sample’s acidity was preserved.When tested in a continuously flowed slurry reactor,the catalyst lifetime for isobutane alkylation was found to be linearly related to the strong Brønsted acid concentration.In addition,Ce^(3+)was found more benefit for the hydride transfer compared with La^(3+),which is ascribed to the stronger polarization effect on the CH bond of isobutane.Moreover,the decline of hydride transfer activity can be slowed down by the catalytic cracking of the bulky molecules.Based on the product distribution,a new catalytic cycle of dimethylhexanes(DMHs)involving a direct formation of isobutene rather than tert-butyl carbocation was proposed in isobutane alkylation.展开更多
The influences of roasting activation on the particle morphology, microscopic structure, and adsorption properties of natural clinoptilolites were investigated. The experimental results show that the optimal modified ...The influences of roasting activation on the particle morphology, microscopic structure, and adsorption properties of natural clinoptilolites were investigated. The experimental results show that the optimal modified conditions include a calcination temperature at 400 ℃, a roasting time of 0.5 h, and furnace cooling. The ammonia nitrogen removal rate from analog renewable water of the modified clinoptilolites reached 72% in the optimized conditions, which is 12% higher than that of natural ones. Scanning electron microscopy analysis showed that the surface morphology changed, the micro-hole size increased, and the surface became smoother and more uniform after calcination. The single-point total adsorption average pore width increased from 7.74 nm to 10.64 nm.展开更多
Calcination and acid leaching of coal kaolin were studied to determine an effective and economical preparation method of calcined kaolin. Thermogravimetric–differential thermal analysis(TG–DTA) and X-ray diffraction...Calcination and acid leaching of coal kaolin were studied to determine an effective and economical preparation method of calcined kaolin. Thermogravimetric–differential thermal analysis(TG–DTA) and X-ray diffraction(XRD) demonstrated that 900°C was the suitable temperature for the calcination. Leaching tests showed that hydrochloric acid was more effective for iron dissolution from raw coal kaolin(RCK), whereas oxalic acid was more effective on iron dissolution from calcined coal kaolin(CCK). The iron dissolution from CCK was 28.78wt%, which is far less effective than the 54.86wt% of RCK under their respective optimal conditions. Through analysis by using M?ssbauer spectroscopy, it is detected that nearly all of the structural ferrous ions in RCK were removed by hydrochloric acid. However, iron sites in CCK changed slightly by oxalic acid leaching because nearly all ferrous ions were transformed into ferric species after firing at 900°C. It can be concluded that it is difficult to remove the structural ferric ions and ferric oxides evolved from the structural ferrous ions. Thus, iron removal by acids should be conducted prior to calcination.展开更多
SiO2-supported Ni-Mo bimetallic phosphides were prepared by temperature-programmed reduction(TPR) method from the phosphate precursors calcined at different temperatures. Their properties were characterized by means o...SiO2-supported Ni-Mo bimetallic phosphides were prepared by temperature-programmed reduction(TPR) method from the phosphate precursors calcined at different temperatures. Their properties were characterized by means of ultraviolet-visible diffuse reflectance spectroscopy(UV-Vis DRS), H2temperature-programmed reduction(H2-TPR), X-ray diffraction(XRD), transmission electron microscopy(TEM), CO chemisorption, H2 and NH3temperature-programmed desorptions(H2-TPD and NH3-TPD). Their catalytic performances for the deoxygenation of methyl laurate were tested in a fixed-bed reactor. When the precursors were calcined at 400 and 500?C, respectively, Ni Mo P2 phase could be formed apart from Ni2 P and Mo P phases in the prepared C400 and C500 catalysts. However, when the precursors were calcined at600, 700 and 800°C, respectively, only Ni2 P and Mo P phases could be detected in the prepared C600, C700 and C800 catalysts. Also, in C400, C500 and C600 catalysts, Mo atoms were found to be entered in the lattice of Ni2 P phase, but the entering extent became less with the increase of calcination temperature. As the calcination temperature of the precursor increased, the interaction between Ni and Mo in the prepared catalysts decreased, and the phosphide crystallite size tended to increase, subsequently leading to the decrease in the surface metal site density and the acid amount. C600 catalyst showed the highest activity among the tested ones for the deoxygenation of methyl laurate. As the calcination temperature of the precursor increased, the selectivity to C12 hydrocarbons decreased while the selectivity to C11 hydrocarbons tended to increase. This can be mainly attributed to the decreased Ni-Mo interaction and the increased phosphide particle size. In sum, the structure and performance of Ni-Mo bimetallic phosphide catalyst can be tuned by the calcination temperature of precursor.展开更多
The desulfurization efficiency and mechanism of the calcination of petroleum coke in ammonia atmosphere at lower than 1000 ℃ were investigated through a series of conditional experiments and comparison with other gas...The desulfurization efficiency and mechanism of the calcination of petroleum coke in ammonia atmosphere at lower than 1000 ℃ were investigated through a series of conditional experiments and comparison with other gases such as H_2. The topics of efficiency and reaction mechanism are usually discussed through investigation by means of the Fourier transform infrared spectroscopy(FT-IR), the Brunauer-Emmett-Teller(BET) technique, and the thermogravimetry coupled with the mass spectrometry(TG-MS). Results showed that in addition to H_2, ammonia not only could retain a high desulfurization rate but could also reduce coke loss during the desulfurization process of petroleum coke. The best desulfurization conditions covered a petroleum coke particle size of less than 0.1 mm, a calcination temperature of 800 ℃ in ammonia atmosphere with a flow rate of 10 L/h, and a heating duration of more than 120 min. Ammonia decomposition, H_2 generation, decline in the activation energy of the carbon–sulfur bonds, and petroleum coke with a largest specific surface area at 800 ℃ are the key goals of desulfurization studied thereby. As proved by TG-MS analysis, given a large quantity of H_2, ammonia can be decomposed at the same temperature to completely come into contact with the sulfur species in petroleum coke to generate H_2S.展开更多
Magnetic α-Fe2O3,γ-Fe2O3 and Fe3O4 were prepared by facile calcination under different temperature from K4[Fe(CN)6]as raw materials,in which the calcined products areα-Fe2O3,Fe3O4 and γ-Fe2O3 at 400 or 700,500,and...Magnetic α-Fe2O3,γ-Fe2O3 and Fe3O4 were prepared by facile calcination under different temperature from K4[Fe(CN)6]as raw materials,in which the calcined products areα-Fe2O3,Fe3O4 and γ-Fe2O3 at 400 or 700,500,and 600 ℃,respectively.The as-prepared compounds were characterized by X-ray powder diffraction and scanning electron microscopy,and their magnetic behavior at room temperature was also studied.This method provided a simple approach to prepare different polymorphic forms of magnetic iron oxides,which may have potential applications in magnetic science,magnetic composite materials,magnetic core,magnetic separation and medical diagnostics.展开更多
The catalytic performances of Co3O4/SiO2 catalysts prepared by incipient wetness impregnation for CO oxidation were investigated using three kinds of silica as carriers with different pore sizes of 7.7,14.0 and 27.0 n...The catalytic performances of Co3O4/SiO2 catalysts prepared by incipient wetness impregnation for CO oxidation were investigated using three kinds of silica as carriers with different pore sizes of 7.7,14.0 and 27.0 nm.The effects of calcination temperature on the catalyst surface and micro structure properties as well as catalytic performance for the oxidation of carbon monoxide were also studied.All catalysts were characterized by N2 adsorption-desorption,XRD,XPS,FTIR,H2-TPR and O2-TPD.It was found that the properties and crystal size of cobalt-containing species strongly depended on the pore size of silica carrier.While the silica pore size increased from 7.7 to 27.0 nm,the Co3O4 crystal size increased from 8.5 to 13.5 nm.Moreover,it was demonstrated that if the spinel crystal structure of Co3O4 was obtained at a calcination temperature as low as 150℃,the catalyst sample would have a high Co3O4 surface dispersion and an increase of surface active species,and thus exhibit a high activity for the oxidation of carbon monoxide.展开更多
In the present work,the effect of pre-calcination on carbonation conversion and cyclic stability of modi fied CaObased sorbent was investigated by thermogravimetric analyzer(TGA).The modi fied CaO-based sorbents with ...In the present work,the effect of pre-calcination on carbonation conversion and cyclic stability of modi fied CaObased sorbent was investigated by thermogravimetric analyzer(TGA).The modi fied CaO-based sorbents with CaAc_2 as precursor were respectively doped with different elements(Mg,Al,Ce,Zr and La).The speci fic surface area,pore volume and pore size distribution were tested by N_2 isothermal adsorption measurements.The phase compositions of sorbents were characterized by X-ray diffraction(XRD).The results showed that the cyclic stabilities of the sorbents were improved by pre-calcination.The pre-calcination was conducted at 900°C for 5 h in air by the muf fle furnace.With pre-calcination,the cyclic stabilities of sorbents could be as high as 96% after 22 cycles,such as CaO-Al,CaO-Ce and CaO-La.After contact with air,the carbonation conversions of spent sorbents with pre-calcination suddenly increased by about one-sixth due to the change of channel structure by hydration.Both the cyclic stability of sorbent and the durability of reactivation were related to the structural stability of sample,especially the stability of mesopores between 2 nm and 5.5 nm.The present work also provided an easy and low-cost method for reactivating the spent CaO-based sorbents.展开更多
The layered perovskite type oxide K2La2Ti3O10 powders were prepared under air, Ar and H2 calcination atmospheres by sol-gel method and characterized by X-ray diffractometry, UV-Vis diffuse reflectance and X-ray photoe...The layered perovskite type oxide K2La2Ti3O10 powders were prepared under air, Ar and H2 calcination atmospheres by sol-gel method and characterized by X-ray diffractometry, UV-Vis diffuse reflectance and X-ray photoelectron spectroscopy. The influence of the calcination atmosphere on the photocatalytic reactivity of K2La2Ti3O10 for hydrogen production was investigated. The photocatalytic reactivity of K2La2Ti3O10 prepared under air, Ar and H2 atmospheres was compared with that prepared under ultraviolet and visible light radiation using I- as electronic donor. The results show that K2La2Ti3O10 prepared under Ar and H2 atmospheres has higher photocatalytic activity for hydrogen production than that prepared under air atmosphere. The hydrogen production rates under ultraviolet irradiation are 127.5, 81.3 and 57.0 μmol/(L·h) and those under visible light irradiation are 40.2, 30.2 and 16.5 μmol/(L·h) respectively when K2La2Ti3O10 is prepared under Ar, H2 and air atmospheres.展开更多
The preparation of microsized hematite powder from ferrous sulfate using microwave calcination was investigated based on the TG/DTG curves. The decomposition of industrial ferrous sulfate under air atmosphere was divi...The preparation of microsized hematite powder from ferrous sulfate using microwave calcination was investigated based on the TG/DTG curves. The decomposition of industrial ferrous sulfate under air atmosphere was divided into three stages, and a ferrous sulfate sample added with 15% Fe_2O_3 could strongly absorb microwave energy. Therefore, preparing hematite powder from ferrous sulfate using microwave calcination was feasible. Hematite was obtained under the following optimized conditions: calcination temperature, 850 °C; microwave power, 650 W; and sample amount, 40 g. The obtained hematite satisfied the first-grade quality requirements. The total ferrum value was more than 58%, and the total sulfur and phosphorus contents were less than 0.5% and 0.2%, respectively. X-ray powder diffraction and scanning electron microscopy were used to characterize the structure and morphology of microsized hematite powder. The particles were non-spherical in shape, and the average particle size distribution was 10.45 μm. This work provides new potential applications for waste ferrous sulfate.展开更多
A new magnesium phosphate bone cement(MPBC) was prepared as a byproduct of boroncontaining magnesium oxide(B-MgO) after extracting Li_2CO_3 from salt lakes. We analyzed the elementary composition of the B-MgO raw mate...A new magnesium phosphate bone cement(MPBC) was prepared as a byproduct of boroncontaining magnesium oxide(B-MgO) after extracting Li_2CO_3 from salt lakes. We analyzed the elementary composition of the B-MgO raw materials and the effects of calcination temperature on the performance of MPBC. The phase composition and microstructure of the B-MgO raw materials and the hydration products(KMg PO_4·6H_2O) of MPBC were analyzed by X-ray diffraction and scanning electron microscopy. The results showed that ionic impurities and the levels of toxic elements were sufficiently low in B-MgO raw materials to meet the medical requirements for Mg O(Chinese Pharmacopeia, 2010 Edition) and for hydroxyapatite surgical implants(GB23101.1-2008). The temperature of B-Mg O calcination had a marked influence on the hydration and hardening of MPBC pastes. Increasing calcination temperature prolonged the time required for the MPBC slurry to set, significantly decreased the hydration temperature, and prolonged the time required to reach the highest hydration temperature. However, the compressive strength of hardened MPBC did not increase with higher calcination temperatures. In the 900-1 000 ℃ temperature range, the hardened MPBC had a higher compressive strength. Imaging analysis suggested that the setting time and the highest hydration temperature of MPBC pastes were dependent on the size and crystal morphology of the B-Mg O materials. The production and microstructure compactness of KMgPO_4·6H_2O, the main hydration product, determined the compressive strength.展开更多
The calcination zone temperature control is an important problem in rotary kiln production process. In order to solve this problem,a predictive control method based on improved harmony search algorithm( IHS)and least ...The calcination zone temperature control is an important problem in rotary kiln production process. In order to solve this problem,a predictive control method based on improved harmony search algorithm( IHS)and least square support vector machine( LSSVM) is proposed. LSSVM is utilized to bulid the nonlinear predictive model of calcination zone temperature in rotary kiln. The calcination zone temperature can be predicted through input control variable,the error and error correction of output feedback. The performance index function is established by deviation and control variable. An IHS algorithm with better fitness and faster convergence speed is proposed. The optimal control variable can be obtained by rolling optimization through this IHS algorithm. The stability of this predictive control method is proved to be feasible. The simulation and actual experiment results show that the proposed predictive control method has good control performance.展开更多
The effect of support calcination temperature on the benzene selective hydrogenation performance of the Ru-Ce-B/ZrO2 catalysts was investigated.It was found that with increasing calcination temperature,the surface are...The effect of support calcination temperature on the benzene selective hydrogenation performance of the Ru-Ce-B/ZrO2 catalysts was investigated.It was found that with increasing calcination temperature,the surface area decreased,on the contrary,the pore size and the amount of monoclinic phase increased.With increasing support calcination temperature,the activity of the catalyst roughly decreased and cyclohexene selectivity increased.The activity decreased due to the decrease of the surface areas.The increase of the cyclohexene selectivity was correlated not only with the decrease of the surface areas but also with the increase of monoclinic phases,rich in surface hydroxyl,and the enlarged pore size of zirconia.This suggests the monoclinic zirconia with a medium surface area,rather than a big one,and a mesoporous structure,even including some macropores,is an ideal support of the catalyst for benzene selective hydrogenation.展开更多
In this paper,the effect of high temperature calcination on the structure and properties of bauxite-based homogeneous clinkers calcined at different temperatures for different durations was studied.The results show th...In this paper,the effect of high temperature calcination on the structure and properties of bauxite-based homogeneous clinkers calcined at different temperatures for different durations was studied.The results show that with the rising of calcination temperature and the prolonging of holding time,the volume density of bauxite-based homogeneous clinkers increases and the apparent porosity decreases.After high temperature calcination,the linear expansion of bauxitebased homogeneous clinker is smaller than that of the non-calcined ones.Whether calcined at high temperatures or not,the thermal shock resistance of bauxite-based homogeneous clinkers is good.The crystalline phases of bauxite-based homogeneous clinkers are mainly mullite and corundum.There is more glass phase in the bauxite-based homogeneous clinkers without calcination.After calcination at high temperatures the glass phase content decreases significantly,and the mullite crystals develop better forming the cross-network structure.展开更多
基金supported by the Chinese Nonferrous Guilin Research Institute of Geology for Mineral Resource (No.ky20101372000001)
文摘Muscovite mineral was roasted in different conditions.Rubidium leaching rate was a standard to examine the impact of various factors on calcination effect,including the agent types,roasting time,mass ratio,and roasting temperature.The results indicate that the best agent is the combination of sodium chloride and calcium chloride,and its mass ratio of muscovite/NaCl/CaCl2is1.00:0.25:0.25.Calcined at 850℃ for 30 min,the rubidium leaching rate is up to 90.12%.The reaction of muscovite ore with the chlorinating agent CaCl2was studied by TG/DSC,and the surface morphology before and after leaching was characterized by SEM.Rubidium chloride products can be obtained using t-BAMBP extraction,hydrochloric acid re-extraction,and purification.
基金Supported by the National Natural Science Foundation of China (No. 50874029)Important Project of Education Ministry (No.307009)National Basic Research Program (973) (No.2007CB613504)
文摘Perovskite-type V-doped titanium-bearing blast furnace slag (VTBBFS) photocatalyst was prepared by high-temperature solid phase method.The influence of calcination temperature on the photocatalytic and antibacterial properties of VTBBFS was studied in details.Its composition and microstructure were evaluated by X-ray diffractometer,ultraviolet-visible absorption spectrometer,Fourier transform infrared spectrometer and scanning electron microscope.The antibacterial properties of VTBBFS to Candida albicans were investigated by flask oscillation method.The results showed that the optical absorption and antibacterial properties of VTBBFS were the best with 10%(ω) doping of vanadium,prepared at 800℃ for 2 h,and its sterilization rate was close to 100% to Candida albicans (ATCC10231).The minimum inhibitory and minimum bactericidal concentrations were 25 and 50 mg/mL.When the concentration was 0.2 μg/mL,the catalyst had the least toxic toxicity.
基金Supported by the National Natural Science Foundation of China(21276123,21490581)the National High Technology Research and Development Program of China(2012AA03A606)the“Summit of the Six Top Talents”Program of Jiangsu Province.
文摘Pd-doped organosilica membranes were prepared by controlling calcination atmospheres(i.e.POS-Air,POS-N2,POS-H2,POS-H2/N2)to tailor their networks for improving their gas separation performance.This study shows that Pd(Ⅱ)could be only maintained under non-reductive calcination atmosphere,while inert and reducing calcination atmosphere is more beneficial to maintain organosilica moieties in POS networks.POS-H2/N2 membrane showed the optimal H2 separation performance that its permselectivities for H2/CO2,H2/N2,H2/CH4 and H2/SF6 are 15.0,96.7,173.0 and 3400.0,re spectively.Moreover,it is found that H2 molecules pass through the four membranes based on activated diffusion,while CO2 molecules permeation through POS-N2 and POS-Air membrane is dominated by surface diffusion.This work may provide insight into the understanding of the calcination atmosphere effect on gas separation performance of metal-doped organosilica membranes.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.U1812402,51664005,and 51774102)Talents of Guizhou Science and Technology Cooperation Platform(Talent Team Giant[2015]4005,Platform Talent[2017]5788,[2017]5626,and KY(2015)334).
文摘To enable the utilization of low-grade and high-sulfur bauxite, the suspension calcination was used to remove the sulfur and the activate silica minerals, and the calcinated bauxite was subjected to a desilication process in Na OH solution under atmospheric pressure. The desulfurization and desilication properties and mineralogical evolution were studied by X-ray diffraction, thermogravimetry–differential thermal analysis, scanning electron microscopy, and FactSage methods. The results demonstrate that the suspension calcination method is efficient for sulfur removal: 84.21% of S was removed after calcination at 1000°C for 2 min. During the calcination process, diaspore and pyrite were transferred to α-Al2O3, magnetite, and hematite. The phase transformation of pyrite follows the order FeS2 → Fe3O4 → Fe2O3, and the iron oxides and silica were converted into iron silicate. In the alkali-soluble desilication process, the optimum condition was an alkali solution concentration of 110 g/L, a reaction time of 20 min, and a reaction temperature of 95°C. The corresponding desilication ratio and alumina loss ratio were 44.9% and 2.4%, respectively, and the alumina-to-silica mass ratio of the concentrate was 7.9. The Al2O3·2SiO2, SiO2, and Al2O3 formed during the calcination process could react with Na OH solution, and their activity decreased in the order of Al2O3·2 SiO2, SiO2, and Al2O3.
文摘Co_3O_4/CeO_2 composites with high surface areas and ultrafine crystalline sizes for catalytic combustion of methane were firstly prepared by a new sol-gel method which combined ultrasonic impregnation treatment and calcination in N_2 atmosphere. The samples were characterized by various means such as nitrogen adsorption/desorption, X-ray diffraction(XRD), H_2 temperature-programmed reduction(H_2-TPR),X-ray photoelectron spectroscopy(XPS) and transmission electron microscopy(TEM). Results showed that the modified catalyst had the mesoporous structure, comparatively higher amount of surface oxygen and larger oxygen vacancies than others. As a result of the structure and surface composition merits, a high methane combustion conversion(50%) could be obtained at a low temperature of 262 °C for the modified Co_3O_4/CeO_2 composites catalysts. The experimental results demonstrated that ultrasonic impregnation treatment combined with the N_2 thermal treatment prior to calcination in air had a promising application for preparation of Co_3O_4/CeO_2 composites catalysts for low-temperature catalytic combustion of methane.
基金This work was supported by the National Key Research and Development Program of China(2017YFA0206803)the National Natural Science Foundation of China(21878315)+3 种基金the Key Programs of the Chinese Academy of Sciences(KFZD-SW-413)the Key Programs of Innovation Academy for Green Manufacture,CAS(IAGM2020C17)K.C.Wong Education Foundation(No.GJTD-2018-04)the Major Program of National Natural Science Foundation of China(21890762).
文摘Lanthanum-containing(LaX)and cerium-containing X zeolites(CeX)were prepared by a doubleexchange,double-calcination method.By changing the calcination atmospheres between nitrogen and air,the Ce^(IV) contents in CeX zeolites were adjusted and their impacts on physicochemical properties and catalytic performance in isobutane alkylation were established.The crystallinity of CeX zeolite was found to be negatively correlated with the Ce^(IV) content.This i s believed to be due to the water formed during the oxidation of Ce^(III),which facilitates the framework dealumination.As a consequence,calcining in air resulted in a great elimination of strong Brønsted acid sites while under nitrogen protection,this phenomenon was mostly hindered and the sample’s acidity was preserved.When tested in a continuously flowed slurry reactor,the catalyst lifetime for isobutane alkylation was found to be linearly related to the strong Brønsted acid concentration.In addition,Ce^(3+)was found more benefit for the hydride transfer compared with La^(3+),which is ascribed to the stronger polarization effect on the CH bond of isobutane.Moreover,the decline of hydride transfer activity can be slowed down by the catalytic cracking of the bulky molecules.Based on the product distribution,a new catalytic cycle of dimethylhexanes(DMHs)involving a direct formation of isobutene rather than tert-butyl carbocation was proposed in isobutane alkylation.
基金Funded by the National Natural Science Foundation of China(No.51174017)
文摘The influences of roasting activation on the particle morphology, microscopic structure, and adsorption properties of natural clinoptilolites were investigated. The experimental results show that the optimal modified conditions include a calcination temperature at 400 ℃, a roasting time of 0.5 h, and furnace cooling. The ammonia nitrogen removal rate from analog renewable water of the modified clinoptilolites reached 72% in the optimized conditions, which is 12% higher than that of natural ones. Scanning electron microscopy analysis showed that the surface morphology changed, the micro-hole size increased, and the surface became smoother and more uniform after calcination. The single-point total adsorption average pore width increased from 7.74 nm to 10.64 nm.
基金financially supported by Zhejiang Natural Science Foundation(No.Y1080393)Opening Foundation of State Key Laboratory of Clean Energy Utilization(No.ZJUEDU2012001)
文摘Calcination and acid leaching of coal kaolin were studied to determine an effective and economical preparation method of calcined kaolin. Thermogravimetric–differential thermal analysis(TG–DTA) and X-ray diffraction(XRD) demonstrated that 900°C was the suitable temperature for the calcination. Leaching tests showed that hydrochloric acid was more effective for iron dissolution from raw coal kaolin(RCK), whereas oxalic acid was more effective on iron dissolution from calcined coal kaolin(CCK). The iron dissolution from CCK was 28.78wt%, which is far less effective than the 54.86wt% of RCK under their respective optimal conditions. Through analysis by using M?ssbauer spectroscopy, it is detected that nearly all of the structural ferrous ions in RCK were removed by hydrochloric acid. However, iron sites in CCK changed slightly by oxalic acid leaching because nearly all ferrous ions were transformed into ferric species after firing at 900°C. It can be concluded that it is difficult to remove the structural ferric ions and ferric oxides evolved from the structural ferrous ions. Thus, iron removal by acids should be conducted prior to calcination.
基金supported by the National Natural Science Foundation of China(No.21176177)the Natural Science Foundation of Tianjin(No.12JCYBJC13200)State Key Laboratory of Catalytic Materials and Reaction Engineering(RIPP,SINOPEC)
文摘SiO2-supported Ni-Mo bimetallic phosphides were prepared by temperature-programmed reduction(TPR) method from the phosphate precursors calcined at different temperatures. Their properties were characterized by means of ultraviolet-visible diffuse reflectance spectroscopy(UV-Vis DRS), H2temperature-programmed reduction(H2-TPR), X-ray diffraction(XRD), transmission electron microscopy(TEM), CO chemisorption, H2 and NH3temperature-programmed desorptions(H2-TPD and NH3-TPD). Their catalytic performances for the deoxygenation of methyl laurate were tested in a fixed-bed reactor. When the precursors were calcined at 400 and 500?C, respectively, Ni Mo P2 phase could be formed apart from Ni2 P and Mo P phases in the prepared C400 and C500 catalysts. However, when the precursors were calcined at600, 700 and 800°C, respectively, only Ni2 P and Mo P phases could be detected in the prepared C600, C700 and C800 catalysts. Also, in C400, C500 and C600 catalysts, Mo atoms were found to be entered in the lattice of Ni2 P phase, but the entering extent became less with the increase of calcination temperature. As the calcination temperature of the precursor increased, the interaction between Ni and Mo in the prepared catalysts decreased, and the phosphide crystallite size tended to increase, subsequently leading to the decrease in the surface metal site density and the acid amount. C600 catalyst showed the highest activity among the tested ones for the deoxygenation of methyl laurate. As the calcination temperature of the precursor increased, the selectivity to C12 hydrocarbons decreased while the selectivity to C11 hydrocarbons tended to increase. This can be mainly attributed to the decreased Ni-Mo interaction and the increased phosphide particle size. In sum, the structure and performance of Ni-Mo bimetallic phosphide catalyst can be tuned by the calcination temperature of precursor.
基金the National Natural Science Foundation of China(Projects No.51374253 and No.51574289)
文摘The desulfurization efficiency and mechanism of the calcination of petroleum coke in ammonia atmosphere at lower than 1000 ℃ were investigated through a series of conditional experiments and comparison with other gases such as H_2. The topics of efficiency and reaction mechanism are usually discussed through investigation by means of the Fourier transform infrared spectroscopy(FT-IR), the Brunauer-Emmett-Teller(BET) technique, and the thermogravimetry coupled with the mass spectrometry(TG-MS). Results showed that in addition to H_2, ammonia not only could retain a high desulfurization rate but could also reduce coke loss during the desulfurization process of petroleum coke. The best desulfurization conditions covered a petroleum coke particle size of less than 0.1 mm, a calcination temperature of 800 ℃ in ammonia atmosphere with a flow rate of 10 L/h, and a heating duration of more than 120 min. Ammonia decomposition, H_2 generation, decline in the activation energy of the carbon–sulfur bonds, and petroleum coke with a largest specific surface area at 800 ℃ are the key goals of desulfurization studied thereby. As proved by TG-MS analysis, given a large quantity of H_2, ammonia can be decomposed at the same temperature to completely come into contact with the sulfur species in petroleum coke to generate H_2S.
基金supported by the Funds of Fujian province department of education(No.JA14199)
文摘Magnetic α-Fe2O3,γ-Fe2O3 and Fe3O4 were prepared by facile calcination under different temperature from K4[Fe(CN)6]as raw materials,in which the calcined products areα-Fe2O3,Fe3O4 and γ-Fe2O3 at 400 or 700,500,and 600 ℃,respectively.The as-prepared compounds were characterized by X-ray powder diffraction and scanning electron microscopy,and their magnetic behavior at room temperature was also studied.This method provided a simple approach to prepare different polymorphic forms of magnetic iron oxides,which may have potential applications in magnetic science,magnetic composite materials,magnetic core,magnetic separation and medical diagnostics.
基金supported by the National Natural Science Foundation of China(NSFC 20776089)the 985 Project of Sichuan University
文摘The catalytic performances of Co3O4/SiO2 catalysts prepared by incipient wetness impregnation for CO oxidation were investigated using three kinds of silica as carriers with different pore sizes of 7.7,14.0 and 27.0 nm.The effects of calcination temperature on the catalyst surface and micro structure properties as well as catalytic performance for the oxidation of carbon monoxide were also studied.All catalysts were characterized by N2 adsorption-desorption,XRD,XPS,FTIR,H2-TPR and O2-TPD.It was found that the properties and crystal size of cobalt-containing species strongly depended on the pore size of silica carrier.While the silica pore size increased from 7.7 to 27.0 nm,the Co3O4 crystal size increased from 8.5 to 13.5 nm.Moreover,it was demonstrated that if the spinel crystal structure of Co3O4 was obtained at a calcination temperature as low as 150℃,the catalyst sample would have a high Co3O4 surface dispersion and an increase of surface active species,and thus exhibit a high activity for the oxidation of carbon monoxide.
基金Supported by Capture CO2 and Storage Technology Jointly Studied by USA and China(2013DFB60140-04)Key Program of National Natural Science Foundation of China(No.21536009)
文摘In the present work,the effect of pre-calcination on carbonation conversion and cyclic stability of modi fied CaObased sorbent was investigated by thermogravimetric analyzer(TGA).The modi fied CaO-based sorbents with CaAc_2 as precursor were respectively doped with different elements(Mg,Al,Ce,Zr and La).The speci fic surface area,pore volume and pore size distribution were tested by N_2 isothermal adsorption measurements.The phase compositions of sorbents were characterized by X-ray diffraction(XRD).The results showed that the cyclic stabilities of the sorbents were improved by pre-calcination.The pre-calcination was conducted at 900°C for 5 h in air by the muf fle furnace.With pre-calcination,the cyclic stabilities of sorbents could be as high as 96% after 22 cycles,such as CaO-Al,CaO-Ce and CaO-La.After contact with air,the carbonation conversions of spent sorbents with pre-calcination suddenly increased by about one-sixth due to the change of channel structure by hydration.Both the cyclic stability of sorbent and the durability of reactivation were related to the structural stability of sample,especially the stability of mesopores between 2 nm and 5.5 nm.The present work also provided an easy and low-cost method for reactivating the spent CaO-based sorbents.
基金Project(2002AA327140) supported by the National High-Tech Research and Development Program of China
文摘The layered perovskite type oxide K2La2Ti3O10 powders were prepared under air, Ar and H2 calcination atmospheres by sol-gel method and characterized by X-ray diffractometry, UV-Vis diffuse reflectance and X-ray photoelectron spectroscopy. The influence of the calcination atmosphere on the photocatalytic reactivity of K2La2Ti3O10 for hydrogen production was investigated. The photocatalytic reactivity of K2La2Ti3O10 prepared under air, Ar and H2 atmospheres was compared with that prepared under ultraviolet and visible light radiation using I- as electronic donor. The results show that K2La2Ti3O10 prepared under Ar and H2 atmospheres has higher photocatalytic activity for hydrogen production than that prepared under air atmosphere. The hydrogen production rates under ultraviolet irradiation are 127.5, 81.3 and 57.0 μmol/(L·h) and those under visible light irradiation are 40.2, 30.2 and 16.5 μmol/(L·h) respectively when K2La2Ti3O10 is prepared under Ar, H2 and air atmospheres.
基金Project(2013AA064003)supported by the National Technology Research and Development Program of ChinaProject(51564033)supported by the National Natural Science Foundation of ChinaProject(2016FA023)supported by the Yunnan Applied Basic Research(CNMRCUXT1403)State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization,Kunming University of Science and Technology,China
文摘The preparation of microsized hematite powder from ferrous sulfate using microwave calcination was investigated based on the TG/DTG curves. The decomposition of industrial ferrous sulfate under air atmosphere was divided into three stages, and a ferrous sulfate sample added with 15% Fe_2O_3 could strongly absorb microwave energy. Therefore, preparing hematite powder from ferrous sulfate using microwave calcination was feasible. Hematite was obtained under the following optimized conditions: calcination temperature, 850 °C; microwave power, 650 W; and sample amount, 40 g. The obtained hematite satisfied the first-grade quality requirements. The total ferrum value was more than 58%, and the total sulfur and phosphorus contents were less than 0.5% and 0.2%, respectively. X-ray powder diffraction and scanning electron microscopy were used to characterize the structure and morphology of microsized hematite powder. The particles were non-spherical in shape, and the average particle size distribution was 10.45 μm. This work provides new potential applications for waste ferrous sulfate.
基金Funded by the National Natural Science Foundation of China(No.21276264)the Qinghai Province Science and TechnologyDepartment(No.2013-G-208)
文摘A new magnesium phosphate bone cement(MPBC) was prepared as a byproduct of boroncontaining magnesium oxide(B-MgO) after extracting Li_2CO_3 from salt lakes. We analyzed the elementary composition of the B-MgO raw materials and the effects of calcination temperature on the performance of MPBC. The phase composition and microstructure of the B-MgO raw materials and the hydration products(KMg PO_4·6H_2O) of MPBC were analyzed by X-ray diffraction and scanning electron microscopy. The results showed that ionic impurities and the levels of toxic elements were sufficiently low in B-MgO raw materials to meet the medical requirements for Mg O(Chinese Pharmacopeia, 2010 Edition) and for hydroxyapatite surgical implants(GB23101.1-2008). The temperature of B-Mg O calcination had a marked influence on the hydration and hardening of MPBC pastes. Increasing calcination temperature prolonged the time required for the MPBC slurry to set, significantly decreased the hydration temperature, and prolonged the time required to reach the highest hydration temperature. However, the compressive strength of hardened MPBC did not increase with higher calcination temperatures. In the 900-1 000 ℃ temperature range, the hardened MPBC had a higher compressive strength. Imaging analysis suggested that the setting time and the highest hydration temperature of MPBC pastes were dependent on the size and crystal morphology of the B-Mg O materials. The production and microstructure compactness of KMgPO_4·6H_2O, the main hydration product, determined the compressive strength.
基金Sponsored by National Natural Science Foundation of China(Grant No.61433004)the Liaoning Province Doctor Startup Fund(Grant No.20141070)
文摘The calcination zone temperature control is an important problem in rotary kiln production process. In order to solve this problem,a predictive control method based on improved harmony search algorithm( IHS)and least square support vector machine( LSSVM) is proposed. LSSVM is utilized to bulid the nonlinear predictive model of calcination zone temperature in rotary kiln. The calcination zone temperature can be predicted through input control variable,the error and error correction of output feedback. The performance index function is established by deviation and control variable. An IHS algorithm with better fitness and faster convergence speed is proposed. The optimal control variable can be obtained by rolling optimization through this IHS algorithm. The stability of this predictive control method is proved to be feasible. The simulation and actual experiment results show that the proposed predictive control method has good control performance.
文摘The effect of support calcination temperature on the benzene selective hydrogenation performance of the Ru-Ce-B/ZrO2 catalysts was investigated.It was found that with increasing calcination temperature,the surface area decreased,on the contrary,the pore size and the amount of monoclinic phase increased.With increasing support calcination temperature,the activity of the catalyst roughly decreased and cyclohexene selectivity increased.The activity decreased due to the decrease of the surface areas.The increase of the cyclohexene selectivity was correlated not only with the decrease of the surface areas but also with the increase of monoclinic phases,rich in surface hydroxyl,and the enlarged pore size of zirconia.This suggests the monoclinic zirconia with a medium surface area,rather than a big one,and a mesoporous structure,even including some macropores,is an ideal support of the catalyst for benzene selective hydrogenation.
文摘In this paper,the effect of high temperature calcination on the structure and properties of bauxite-based homogeneous clinkers calcined at different temperatures for different durations was studied.The results show that with the rising of calcination temperature and the prolonging of holding time,the volume density of bauxite-based homogeneous clinkers increases and the apparent porosity decreases.After high temperature calcination,the linear expansion of bauxitebased homogeneous clinker is smaller than that of the non-calcined ones.Whether calcined at high temperatures or not,the thermal shock resistance of bauxite-based homogeneous clinkers is good.The crystalline phases of bauxite-based homogeneous clinkers are mainly mullite and corundum.There is more glass phase in the bauxite-based homogeneous clinkers without calcination.After calcination at high temperatures the glass phase content decreases significantly,and the mullite crystals develop better forming the cross-network structure.
