The adsorptive separation of C_(2)H_(4)and C_(2)H_(6),as an alternative to distillation units consuming high energy,is a promising yet challenging research.The great similarity in the molecular size of C_(2)H_(4)and C...The adsorptive separation of C_(2)H_(4)and C_(2)H_(6),as an alternative to distillation units consuming high energy,is a promising yet challenging research.The great similarity in the molecular size of C_(2)H_(4)and C_(2)H_(6)brings challenges to the regulation of adsorbents to realize efficient dynamic separation.Herein,we reported the enhancement of the kinetic separation of C_(2)H_(4)/C_(2)H_(6)by controlling the crystal size of ZnAtzPO_(4)(Atz=3-amino-1,2,4-triazole)to amplify the diffusion difference of C_(2)H_(4)and C_(2)H_(6).Through adjusting the synthesis temperature,reactant concentration,and ligands/metal ions molar ratio,ZnAtzPO4 crystals with different sizes were obtained.Both single-component kinetic adsorption tests and binary-component dynamic breakthrough experiments confirmed the enhancement of the dynamic separation of C_(2)H_(4)/C_(2)H_(6)with the increase in the crystal size of ZnAtzPO_(4).The separation selectivity of C_(2)H_(4)/C_(2)H_(6)increased from 1.3 to 98.5 with the increase in the crystal size of ZnAtzPO_(4).This work demonstrated the role of morphology and size control of adsorbent crystals in the improvement of the C_(2)H_(4)/C_(2)H_(6)kinetic separation performance.展开更多
Ten rock samples consisting of one pyroclastic density current(PDC1)deposit,seven lava flows(LF1–7),and two summit lava domes(LD1,2)were studied to understand the petrogenesis and magma dynamics at Mt.Sumbing.The str...Ten rock samples consisting of one pyroclastic density current(PDC1)deposit,seven lava flows(LF1–7),and two summit lava domes(LD1,2)were studied to understand the petrogenesis and magma dynamics at Mt.Sumbing.The stratigraphy is arranged as LF1,PDC1,LF2,LF3,LF4,LF5,LF6,LF7,LD1,and LD2;furthermore,these rocks were divided into two types.TypeⅠ,observed in the oldest(LF1)sample,has poor MgO and high Ba/Nb,Th/Yb and Sr.The remaining samples(PDC1–LD2)represent typeⅡ,characterized by high MgO and low Ba/Nb,Th/Yb and Sr values.We suggest that type I is derived from AOC(altered oceanic crust)-rich melts that underwent significant crustal assimilation,while typeⅡoriginates from mantle-rich melts with less significant crustal assimilation.The early stage of typeⅡmagma(PDC1–LF3)was considered a closed system,evolving basaltic andesite into andesite(55.0–60.2 wt%SiO_(2))with a progressively increasing phenocryst(0.30–0.48φ_(PC))and decreasing crystal size distribution(CSD)slope(from-3.9 to-2.9).The evidence of fluctuating silica and phenocryst contents(between 55.9–59.7 wt%and 0.25–0.41φ_(PC),respectively),coupled with the kinked and steep(from-5.0 to-3.3)CSD curves imply the interchanging condition between open(i.e.,magma mixing)and closed magmatic systems during the middle stage(LF4–LF6).Finally,it underwent to closed system again during the final stage(LF7–LD2)because the magma reached dacitic composition(at most 68.9 wt%SiO_(2))with abundant phenocryst(0.38–0.45φ_(PC))and gentle CSD slope(from-4.1 to-1.2).展开更多
The porosity of H‐ZSM‐5zeolite is known to facilitate the diffusion of molecules in the methanol‐to‐aromatics(MTA)reaction.The activity and selectivity of the H‐ZSM‐5catalyst in the MTAreaction has been studied ...The porosity of H‐ZSM‐5zeolite is known to facilitate the diffusion of molecules in the methanol‐to‐aromatics(MTA)reaction.The activity and selectivity of the H‐ZSM‐5catalyst in the MTAreaction has been studied as a function of crystal size.ZSM‐5zeolites with different crystal sizeswere successfully synthesized by conventional hydrothermal methods.Tailoring ZSM‐5particle sizewas easily controlled by changes to the sol‐gel composition,and in particular,the deionized waterto tetrapropylammonium hydroxide ratio,and crystallization time.The structure of the H‐ZSM‐5zeolites were characterized by X‐ray diffraction and the morphology of the zeolite particles wasdetermined by scanning electron microscopy.N2adsorption‐desorption measurements establishedchanges to the textural properties,and compositional properties were characterized by X‐ray fluorescencespectroscopy.Acidity measurements of the catalysts were measured by pyridine‐adsorbedFourier transform infrared spectroscopy and the temperature‐programmed desorption of ammonia.After subjecting the catalysts to the MTA reaction,the total amount of coke formed on the spentdeactivated catalysts was determined by thermal gravimetric analysis.The results show that theSiO2/Al2O3molar ratios and acidic properties of the H‐ZSM‐5samples are similar,however,thenano‐sized hierarchical ZSM‐5zeolite with an additional level of auxiliary pores possesses a higher展开更多
Carbon deposition during methanol to hydrocarbons leads to the quick deactivation of ZSM-5 catalyst and it is one of the major problems for this technology. Decreasing the crystal size or introducing mesopores into ZS...Carbon deposition during methanol to hydrocarbons leads to the quick deactivation of ZSM-5 catalyst and it is one of the major problems for this technology. Decreasing the crystal size or introducing mesopores into ZSM-5 zeolites can improve its diffusion property and decrease the coke formation. In this paper, nano-sized ZSM-5 zeolite with intercrystalline mesopores combining the mesoporous and nano sized structure was fabricated. For comparison, the mesoporous ZSM-5 and nano-sized ZSM-5 were also prepared. These catalyst samples were characterized by XRD, BET, NH3-TPD, TEM, Py-IR and TG techniques and used on the conversion of methanol to gasoline in a fixed-bed reactor at T=405 degrees C, WHSV =4.74 h(-1) and P=1.0 MPa. It was found that the external surface area of the nano-sized ZSM-5 zeolite with intercrystalline mesopores reached 104 m(2)/g, larger than that of mesoporous ZSM-5 (66 m(2)/g) and nano sized ZSM-5 (76 m(2)/g). Catalytic lifetime of the nano-sized ZSM-5 zeolite with intercrystalline mesopores was 93 h, which was only longer than that of mesoporous ZSM-5 (86 h), but shorter than that of nano sized ZSM-5 (104 h). Strong acidity promoted the coke formation and thus decreased the catalytic lifetime of the nano-sized ZSM-5 zeolite with intercrystalline mesopores though it presented large external surface that could improve the diffusion property. The special zeolite catalyst was further dealuminated to decrease the strong acidity. After this, its coke formation rate was slowed and catalytic lifetime was prolonged to 106 h because of the large external surface area and decreased weak acidity. This special structural zeolite is a potential catalyst for methanol to gasoline reaction. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.展开更多
size of spinel crystals in the CaO–SiO2–MgO –Al2O3–Cr2O3 system was investigated using lab experiments carried out in a carbon tube furnace. Scanning electron microscopy with energy-dispersive X-ray spectroscopy（...size of spinel crystals in the CaO–SiO2–MgO –Al2O3–Cr2O3 system was investigated using lab experiments carried out in a carbon tube furnace. Scanning electron microscopy with energy-dispersive X-ray spectroscopy（SEM–EDS） and X-ray diffraction（XRD） were used to analyze the microstructure, components, and the mineral phases of synthetic slags. FactS age 7.1 was used to calculate the crystallization process of the molten slag. The results showed that the addition of Fe2O3 promoted the precipitation of spinel crystals and inhibited the formation of dicalcium silicate. The size of spinel crystals increased from 2.74 to 8.10 μm and the contents of chromium and iron in the spinel varied as the Fe2O3 addition was increased from 0 to 20 wt%. Fe2O3 thermodynamically provided the spinel-forming components to enhance the formation of FeCr2O4, MgFe2O4, and Fe3O4. The addition of Fe2O3 increased the fraction of liquid phase in a certain temperature range and promoted diffusion by decreasing the slag’s viscosity. Therefore, Fe2O3 is beneficial to the growth of spinel crystals in stainless steel slag.展开更多
Calcium modified lead titanate nanocrystal material Pb0.85Ca0.15TiO3 was synthesized by means of a solgel method.The changes of crystal structure and grainsize of the samples were investigated under different conditio...Calcium modified lead titanate nanocrystal material Pb0.85Ca0.15TiO3 was synthesized by means of a solgel method.The changes of crystal structure and grainsize of the samples were investigated under different conditions of heat treatment.the results show that the tetragonal symmetry is reduced and the ferroelectricparaelectric phase transformation temperature is decreased with the reduce of the grainsize of the sample.the critical grainsize for the ferroelectricparaelectric phase transformation at room temperature was calculated.The change regularities of the lattice constant and tetragonality with the grainsize are discussed.展开更多
Fischer-Tropsch synthesis （FTS） is an increasingly important approach for producing liquid fuels and chemicals via syngas-that is, synthesis gas, a mixture of carbon monoxide and hydrogen-generated from coal, natura...Fischer-Tropsch synthesis （FTS） is an increasingly important approach for producing liquid fuels and chemicals via syngas-that is, synthesis gas, a mixture of carbon monoxide and hydrogen-generated from coal, natural gas, or biomass. In FTS, dispersed transition metal nanoparticles are used to catalyze the reactions underlying the formation of carbon-carbon bonds. Catalytic activity and selectivity are strongly correlated with the electronic and geometric structure of the nanoparticles, which depend on the particle size, morphology, and crystallographic phase of the nanoparticles. In this article, we review recent works dealing with the aspects of bulk and surface sensitivity of the FTS reaction. Understanding the different catalytic behavior in more detail as a function of these parameters may guide the design of more active, selective, and stable FTS catalysts.展开更多
In manufacturing process, it is necessary to measure change in CSD (Crystal Size Distribution) with time accurately because CSD is one of the most important indices that evaluate quality of products. FBRM (Focused Bea...In manufacturing process, it is necessary to measure change in CSD (Crystal Size Distribution) with time accurately because CSD is one of the most important indices that evaluate quality of products. FBRM (Focused Beam Reflectance Measurement) can measure CLD (Chord Length Distribution) in line, but CLD is different from CSD because of principle of FBRM. However, if CSD is determined beforehand, CLD can be calculated from the CSD with statistical method. First, when crystal shape is defined from the characteristic crystal size, the matrix of each crystal shape which transforms CSD into CLD in a uniform manner is calculated with Monte Carlo analysis. Characteristic crystal size is added to the variables defining chord length in order to avoid complex integrals and apply the change in crystal shape with characteristic crystal size to the transforming matrix. Secondly, CSD and CLD are actually measured in suspension of acetaminophen in ethanol and suspension of L-arginine in water to demonstrate the validity of 2 matrices. Lastly, these matrices are multiplied by some simple CSD models to test the properties of these matrices and demonstrate the utility of this transformation.展开更多
Ultrasonic technology has been intensively studied recently due to its special features. In this paper, an ultrasonic crystallization method was introduced for the preparation of ZnAl-Hydrotalcite-Like compounds （ZnA...Ultrasonic technology has been intensively studied recently due to its special features. In this paper, an ultrasonic crystallization method was introduced for the preparation of ZnAl-Hydrotalcite-Like compounds （ZnAl-HTLcs）. Samples with high crystallinity, small particle size and narrow particle size distribution were obtained and fully characterized using conventional techniques of XRD, FT-IR and TGDTA. The results prove that both ultrasonic frequency and ultrasonic power have effects on the sizes of the product particles. By varying the ultrasonic power from 250 W to 88 W, with the ultrasonic frequency fixed at 59 kHz, the median particle size of the samples increased from 0.37 μm to 0.82 μm. By altering the hydrothermal treatment time from 1 h to 5 h at 110 ℃, the median particle size of ZnAl-HTLcs synthesized via ultrasonic crystallization increased from 0.88 μm to 1.11 μm.展开更多
Nanocrystalline TiO2 was prepared by high frequency plasma chemical vapor deposition (HF-PCVD). The effects of additive AlCl3 on crystal phase, particle size and microstructurai parameters of TiO2 nanocrystallites wer...Nanocrystalline TiO2 was prepared by high frequency plasma chemical vapor deposition (HF-PCVD). The effects of additive AlCl3 on crystal phase, particle size and microstructurai parameters of TiO2 nanocrystallites were investigated by X-ray diffraction(XRD) and transmission electron microscopy (TEM). The nanocrystallites obtained experimentally are mixture of anatase and rutile, the uniform diameters of particles are about 30 nm. The phase transformation from anatase to rutile was accelerated by AlCl3, and rutile content is increased from 26.7 wt pct to 53.6 wt pct with increasing of addition of AlCl3 from 0.0 wt pct to 5.0 wt pct. The particle size is reduced and the size distribution becomes very narrow. The crystal lattice constants have the trend to decrease, and celi volumes appear as shrinkable.展开更多
Crystal shape distribution, i.e. the multidimensional size distribution of crystals, is of great importance to their down-stream processing such as in filtration as well as to the end-use properties including the diss...Crystal shape distribution, i.e. the multidimensional size distribution of crystals, is of great importance to their down-stream processing such as in filtration as well as to the end-use properties including the dissolution rate and bioavailability for crystalline pharmaceuticals. Engineering crystal shape and shape distribution requires knowledge about the growth behavior of different crystal facets under varied operational conditions e.g. supersaturations. Measurement of the facet growth rates and growth kinetics of static crystals in a crystallizer without stirring has been reported previously. Here attention is given to study on real-time characterization of the 3D facet growth behavior of crystals in a stirred tank where crystals are constantly moving and rotating. The measurement technique is stereo imaging and the crystal shape reconstruction is based on a stereo imaging camera model. By reference to a case study on potash alum crystallization, it is demonstrated that the crystal size and shape distributions (CSSD) of moving and rotating potash alum crystals in the solution can be reconstructed. The moving window approach was used to correlate 3D face growth kinetics with supersaturation (in the range 0.04 - 0.12) given by an ATR FTIR probe. It revealed that {100} is the fastest growing face, leading to a rapid reduction of its area, while the {111} face has the slowest growth rate, reflected in its area continuously getting larger.展开更多
The inhibitory effect of phosphate on the crystal grain growth of nanosized titania during high temperature calcination was investigated. Nanosized titanium dioxide powders prepared by hydrolysis of titanium tetrachlo...The inhibitory effect of phosphate on the crystal grain growth of nanosized titania during high temperature calcination was investigated. Nanosized titanium dioxide powders prepared by hydrolysis of titanium tetrachloride were soaked in phosphate solutions with different concentrations. The obtained powders calcined at various temperatures were characterized by X-ray diffraction （XRD）, Fourier transform infrared spectroscopy （FTIR）, and X-ray photoelectronic spectroscopy （XPS）. The grain size of the samples without phosphate treatment increased quickly when calcined at high temperatures, while the grain size of the samples with phosphate modification increased slowly when calcined at the same temperature. This phenomenon implies that phosphate treatment plays an important role in inhibiting the crystal grain growth of titania. The possible mechanism of the inhibition effect of phosphate on titania is discussed.展开更多
Calcium carbonate, the main component of lime, has been widely used in industry due to its stability and economy. Calcium carbonate has three types of crystalline polymorphism, calcite, aragonite and vaterite, each wi...Calcium carbonate, the main component of lime, has been widely used in industry due to its stability and economy. Calcium carbonate has three types of crystalline polymorphism, calcite, aragonite and vaterite, each with different properties. Therefore, the control of crystal polymorphism is required for industrial applications. In addition, the control of crystal size and shape is similarly required for different applications. In this study, the effect of SrCO<sub>3</sub> on the size control of fine aragonite-type calcium carbonate crystals by uniform urea precipitation and the effect of SrCO<sub>3</sub> addition was investigated by adding solid strontium carbonate and dissolved strontium carbonate. The addition of solid strontium carbonate affected the crystal polymorphism and size of the calcium carbonate produced, depending on the properties of the solid particles and the amount of SrCO<sub>3</sub> added. Experiments on the addition of dissolved SrCO<sub>3</sub> showed that the supersaturation formation rate could be controlled to control the crystal polymorphism.展开更多
The Panzhihua layered intrusions is generated closely related to the Emeishan LIPs.This paper analyzes the spatial distribution of plagioclase and pyroxene.The quantitative texture analysis of 2209 plagioclase shows t...The Panzhihua layered intrusions is generated closely related to the Emeishan LIPs.This paper analyzes the spatial distribution of plagioclase and pyroxene.The quantitative texture analysis of 2209 plagioclase shows that the characteristic length of plagioclase is 0.54 to 0.96 mm,the intercept variation range is large,from-0.67 to 0.96,and the slope is-1.85 to-1.04,the Aspect Ratio shows from 1.84 to 2.59 and fractal dimension D is 1.908–1.933.The quantitative texture analysis of 2342 pyroxene shows that the characteristic length of pyroxene is 0.38–0.64 mm,the intercept shows from 0.46 to 2.26,The slope ranges from-2.6 to-1.47,the Aspect Ratio value varies from 1.53 to 1.71,the fractal dimension D is 0.93 to 1.13.All the CSDs results of the Panzhihua intrusions indicate that plagioclase and pyroxene form in an open magma system and undergo four replenishment of magma injection.The plagioclase crystals do not grow as the lathlike shape,and the fractal growth leads to complex crystal surface.The plagioclase undergoes deformation compaction during the crystal process,and then is oriented.The pyroxene crystals grow along an approximately triaxial ratio and undergo texture adjustment and small crystal dissolution reabsorption.When all crystals in magma system grows up to 2 mm,the pyroxene undergoes cumulation in the Panzhihua layered intrusions.The plagioclase crystallization time scale is 171.23–304.41 years,representing that the crystallization is the more uniform in central part of the melt.The nucleation density continuously increases during the crystallization process of the magma system.The time scale to reach the final maximum crystal nucleation density is 15.28–58.98 years.展开更多
1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was ...1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was much oversupplied[1].However particles anhydrous sodium sulphate of large size is not adequate to the demand for its展开更多
The effect of crystal size of USY zeolite on the performance of hydro-upgrading catalysts for treating catalytically cracked(FCC) LCO(light cycle oil) was studied.Three W-Ni catalysts supported on USY zeolites with di...The effect of crystal size of USY zeolite on the performance of hydro-upgrading catalysts for treating catalytically cracked(FCC) LCO(light cycle oil) was studied.Three W-Ni catalysts supported on USY zeolites with different crystal sizes and Al2O3 were prepared by impregnation method.The catalysts were characterized by XRD and BET methods,and evaluated in a micro-reactor using tetralin as the model compound and in an 100-mL hydrogenation test unit using FCC LCO as the feedstock.By contrast,catalyst made from smaller crystal-size USY zeolite had higher external surface area and shorter pore length,having more hydrogenation activity sites and short contact time of reactant molecules with acidity sites.The evaluation results showed that the catalyst prepared on the basis of small crystal-size USY zeolite had higher tetralin conversion and better hydro-upgrading performance for treating FCC LCO.展开更多
The crystal size distribution（CSD）was determined with small angle X-ray scattering technique.Theanticoking property of Ni-catalysts was investigated with the steam reforming of n-heptane in a TG-monitoredflow reacto...The crystal size distribution（CSD）was determined with small angle X-ray scattering technique.Theanticoking property of Ni-catalysts was investigated with the steam reforming of n-heptane in a TG-monitoredflow reactor.The results of this study show that the rate of coking on the supported Ni-catalysts depends main-ly on the percentage content of the large size fraction（25-70nm）of Ni-crystallites,and that the dispersion ofNi-crystallites and the anticoking property of the Ni/α-Al<sub>2</sub>O<sub>3</sub> catalysts were promoted obviously by theLa<sub>2</sub>O<sub>3</sub>-modification method.The variation of the Ni-CSD and the anticoking property of the catalysts were fur-ther tested through different periods of hydrothermal treatment.It is found that the content of the largeNi-crystal size fraction and the coking rate pass correspondingly through a maximum.展开更多
The size and weight fraction of crystals of pure ice or dimethylsulfoxide (DMSO) in poly(vinyl alcohol) (PVA) gel prepared from a mixed solvent of DMSO/water were determined from melting peaks observed by differential...The size and weight fraction of crystals of pure ice or dimethylsulfoxide (DMSO) in poly(vinyl alcohol) (PVA) gel prepared from a mixed solvent of DMSO/water were determined from melting peaks observed by differential scanning calorimetry (DSC). The depression of the melting point with respect to the equilibrium melting point and the melting enthalpy gave the crystal size and weight fraction, respectively. The sizes were in the range of a few nm to tens of nm, depending on the composition ratio of the mixed solvent (DMSO/water) and the polymer concentration. Based on the weight fraction, the critical condition at which the whole solvent became non-freezable was estimated, and it was found to depend on both the PVA concentration and the DMSO/water ratio. When the solvent was pure water, the critical PVA concentration was as high as 86.4 wt%, while for pure DMSO solvent it was 50.1 wt%.展开更多
A dynamic explicit finite element code and rate-dependent elastic-viscoplastic polycrystalline model were used to simulate the simple tension test of annealing FCC polycrystal and 6111-T4 aluminum alloy sheet metal. T...A dynamic explicit finite element code and rate-dependent elastic-viscoplastic polycrystalline model were used to simulate the simple tension test of annealing FCC polycrystal and 6111-T4 aluminum alloy sheet metal. The variability of flow stress was investigated, which was induced by various grain boundary constraints when the ratio of thickness-to-grain size was changed. The simulated results show that, when the relative grain size increases, the constraint of grain boundary will increase accordingly, which results in the increase of the flow stress of polycrystal. The results agree with experiments.展开更多
基金supported by the National Key Research and Development Program of China(2022YFB3806800)the National Natural Science Foundation of China(22122811,22008209)the Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering(2021SZ-TD008).
文摘The adsorptive separation of C_(2)H_(4)and C_(2)H_(6),as an alternative to distillation units consuming high energy,is a promising yet challenging research.The great similarity in the molecular size of C_(2)H_(4)and C_(2)H_(6)brings challenges to the regulation of adsorbents to realize efficient dynamic separation.Herein,we reported the enhancement of the kinetic separation of C_(2)H_(4)/C_(2)H_(6)by controlling the crystal size of ZnAtzPO_(4)(Atz=3-amino-1,2,4-triazole)to amplify the diffusion difference of C_(2)H_(4)and C_(2)H_(6).Through adjusting the synthesis temperature,reactant concentration,and ligands/metal ions molar ratio,ZnAtzPO4 crystals with different sizes were obtained.Both single-component kinetic adsorption tests and binary-component dynamic breakthrough experiments confirmed the enhancement of the dynamic separation of C_(2)H_(4)/C_(2)H_(6)with the increase in the crystal size of ZnAtzPO_(4).The separation selectivity of C_(2)H_(4)/C_(2)H_(6)increased from 1.3 to 98.5 with the increase in the crystal size of ZnAtzPO_(4).This work demonstrated the role of morphology and size control of adsorbent crystals in the improvement of the C_(2)H_(4)/C_(2)H_(6)kinetic separation performance.
基金funded by the Faculty of Geography under the scheme of“Dana Hibah Penelitian Mandiri Dosen Tahun 2023 Tahap 1”。
文摘Ten rock samples consisting of one pyroclastic density current(PDC1)deposit,seven lava flows(LF1–7),and two summit lava domes(LD1,2)were studied to understand the petrogenesis and magma dynamics at Mt.Sumbing.The stratigraphy is arranged as LF1,PDC1,LF2,LF3,LF4,LF5,LF6,LF7,LD1,and LD2;furthermore,these rocks were divided into two types.TypeⅠ,observed in the oldest(LF1)sample,has poor MgO and high Ba/Nb,Th/Yb and Sr.The remaining samples(PDC1–LD2)represent typeⅡ,characterized by high MgO and low Ba/Nb,Th/Yb and Sr values.We suggest that type I is derived from AOC(altered oceanic crust)-rich melts that underwent significant crustal assimilation,while typeⅡoriginates from mantle-rich melts with less significant crustal assimilation.The early stage of typeⅡmagma(PDC1–LF3)was considered a closed system,evolving basaltic andesite into andesite(55.0–60.2 wt%SiO_(2))with a progressively increasing phenocryst(0.30–0.48φ_(PC))and decreasing crystal size distribution(CSD)slope(from-3.9 to-2.9).The evidence of fluctuating silica and phenocryst contents(between 55.9–59.7 wt%and 0.25–0.41φ_(PC),respectively),coupled with the kinked and steep(from-5.0 to-3.3)CSD curves imply the interchanging condition between open(i.e.,magma mixing)and closed magmatic systems during the middle stage(LF4–LF6).Finally,it underwent to closed system again during the final stage(LF7–LD2)because the magma reached dacitic composition(at most 68.9 wt%SiO_(2))with abundant phenocryst(0.38–0.45φ_(PC))and gentle CSD slope(from-4.1 to-1.2).
基金supported by the National Natural Science Foundation of China (21676300)~~
文摘The porosity of H‐ZSM‐5zeolite is known to facilitate the diffusion of molecules in the methanol‐to‐aromatics(MTA)reaction.The activity and selectivity of the H‐ZSM‐5catalyst in the MTAreaction has been studied as a function of crystal size.ZSM‐5zeolites with different crystal sizeswere successfully synthesized by conventional hydrothermal methods.Tailoring ZSM‐5particle sizewas easily controlled by changes to the sol‐gel composition,and in particular,the deionized waterto tetrapropylammonium hydroxide ratio,and crystallization time.The structure of the H‐ZSM‐5zeolites were characterized by X‐ray diffraction and the morphology of the zeolite particles wasdetermined by scanning electron microscopy.N2adsorption‐desorption measurements establishedchanges to the textural properties,and compositional properties were characterized by X‐ray fluorescencespectroscopy.Acidity measurements of the catalysts were measured by pyridine‐adsorbedFourier transform infrared spectroscopy and the temperature‐programmed desorption of ammonia.After subjecting the catalysts to the MTA reaction,the total amount of coke formed on the spentdeactivated catalysts was determined by thermal gravimetric analysis.The results show that theSiO2/Al2O3molar ratios and acidic properties of the H‐ZSM‐5samples are similar,however,thenano‐sized hierarchical ZSM‐5zeolite with an additional level of auxiliary pores possesses a higher
基金the Science and Technology Foundation Platform Construction Project of Shanxi Province(No.2015091009)the National Science Foundation for Young Scientists of China(No.21606160)+1 种基金the Qualified Personnel Foundation of Taiyuan University of Technology(No.tyut-rc201454a)School Fund of Taiyuan University of Technology(Nos.1205-04020202 and 1205-04020102)
文摘Carbon deposition during methanol to hydrocarbons leads to the quick deactivation of ZSM-5 catalyst and it is one of the major problems for this technology. Decreasing the crystal size or introducing mesopores into ZSM-5 zeolites can improve its diffusion property and decrease the coke formation. In this paper, nano-sized ZSM-5 zeolite with intercrystalline mesopores combining the mesoporous and nano sized structure was fabricated. For comparison, the mesoporous ZSM-5 and nano-sized ZSM-5 were also prepared. These catalyst samples were characterized by XRD, BET, NH3-TPD, TEM, Py-IR and TG techniques and used on the conversion of methanol to gasoline in a fixed-bed reactor at T=405 degrees C, WHSV =4.74 h(-1) and P=1.0 MPa. It was found that the external surface area of the nano-sized ZSM-5 zeolite with intercrystalline mesopores reached 104 m(2)/g, larger than that of mesoporous ZSM-5 (66 m(2)/g) and nano sized ZSM-5 (76 m(2)/g). Catalytic lifetime of the nano-sized ZSM-5 zeolite with intercrystalline mesopores was 93 h, which was only longer than that of mesoporous ZSM-5 (86 h), but shorter than that of nano sized ZSM-5 (104 h). Strong acidity promoted the coke formation and thus decreased the catalytic lifetime of the nano-sized ZSM-5 zeolite with intercrystalline mesopores though it presented large external surface that could improve the diffusion property. The special zeolite catalyst was further dealuminated to decrease the strong acidity. After this, its coke formation rate was slowed and catalytic lifetime was prolonged to 106 h because of the large external surface area and decreased weak acidity. This special structural zeolite is a potential catalyst for methanol to gasoline reaction. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
基金financially supported by the National Natural Science Foundation of China (No. 51404173)Hubei Provincial Natural Science Foundation (No. 2016CFB579)+1 种基金China Postdoctoral Science Foundation (No. 2014M562073)State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology
文摘size of spinel crystals in the CaO–SiO2–MgO –Al2O3–Cr2O3 system was investigated using lab experiments carried out in a carbon tube furnace. Scanning electron microscopy with energy-dispersive X-ray spectroscopy（SEM–EDS） and X-ray diffraction（XRD） were used to analyze the microstructure, components, and the mineral phases of synthetic slags. FactS age 7.1 was used to calculate the crystallization process of the molten slag. The results showed that the addition of Fe2O3 promoted the precipitation of spinel crystals and inhibited the formation of dicalcium silicate. The size of spinel crystals increased from 2.74 to 8.10 μm and the contents of chromium and iron in the spinel varied as the Fe2O3 addition was increased from 0 to 20 wt%. Fe2O3 thermodynamically provided the spinel-forming components to enhance the formation of FeCr2O4, MgFe2O4, and Fe3O4. The addition of Fe2O3 increased the fraction of liquid phase in a certain temperature range and promoted diffusion by decreasing the slag’s viscosity. Therefore, Fe2O3 is beneficial to the growth of spinel crystals in stainless steel slag.
文摘Calcium modified lead titanate nanocrystal material Pb0.85Ca0.15TiO3 was synthesized by means of a solgel method.The changes of crystal structure and grainsize of the samples were investigated under different conditions of heat treatment.the results show that the tetragonal symmetry is reduced and the ferroelectricparaelectric phase transformation temperature is decreased with the reduce of the grainsize of the sample.the critical grainsize for the ferroelectricparaelectric phase transformation at room temperature was calculated.The change regularities of the lattice constant and tetragonality with the grainsize are discussed.
基金financial support by NWO-VICI and NWO-TOP grants awarded to Emiel J.M.Hensen
文摘Fischer-Tropsch synthesis （FTS） is an increasingly important approach for producing liquid fuels and chemicals via syngas-that is, synthesis gas, a mixture of carbon monoxide and hydrogen-generated from coal, natural gas, or biomass. In FTS, dispersed transition metal nanoparticles are used to catalyze the reactions underlying the formation of carbon-carbon bonds. Catalytic activity and selectivity are strongly correlated with the electronic and geometric structure of the nanoparticles, which depend on the particle size, morphology, and crystallographic phase of the nanoparticles. In this article, we review recent works dealing with the aspects of bulk and surface sensitivity of the FTS reaction. Understanding the different catalytic behavior in more detail as a function of these parameters may guide the design of more active, selective, and stable FTS catalysts.
文摘In manufacturing process, it is necessary to measure change in CSD (Crystal Size Distribution) with time accurately because CSD is one of the most important indices that evaluate quality of products. FBRM (Focused Beam Reflectance Measurement) can measure CLD (Chord Length Distribution) in line, but CLD is different from CSD because of principle of FBRM. However, if CSD is determined beforehand, CLD can be calculated from the CSD with statistical method. First, when crystal shape is defined from the characteristic crystal size, the matrix of each crystal shape which transforms CSD into CLD in a uniform manner is calculated with Monte Carlo analysis. Characteristic crystal size is added to the variables defining chord length in order to avoid complex integrals and apply the change in crystal shape with characteristic crystal size to the transforming matrix. Secondly, CSD and CLD are actually measured in suspension of acetaminophen in ethanol and suspension of L-arginine in water to demonstrate the validity of 2 matrices. Lastly, these matrices are multiplied by some simple CSD models to test the properties of these matrices and demonstrate the utility of this transformation.
基金Supported by the Natural Science Funds (20001015) of Xianxi Province.
文摘Ultrasonic technology has been intensively studied recently due to its special features. In this paper, an ultrasonic crystallization method was introduced for the preparation of ZnAl-Hydrotalcite-Like compounds （ZnAl-HTLcs）. Samples with high crystallinity, small particle size and narrow particle size distribution were obtained and fully characterized using conventional techniques of XRD, FT-IR and TGDTA. The results prove that both ultrasonic frequency and ultrasonic power have effects on the sizes of the product particles. By varying the ultrasonic power from 250 W to 88 W, with the ultrasonic frequency fixed at 59 kHz, the median particle size of the samples increased from 0.37 μm to 0.82 μm. By altering the hydrothermal treatment time from 1 h to 5 h at 110 ℃, the median particle size of ZnAl-HTLcs synthesized via ultrasonic crystallization increased from 0.88 μm to 1.11 μm.
文摘Nanocrystalline TiO2 was prepared by high frequency plasma chemical vapor deposition (HF-PCVD). The effects of additive AlCl3 on crystal phase, particle size and microstructurai parameters of TiO2 nanocrystallites were investigated by X-ray diffraction(XRD) and transmission electron microscopy (TEM). The nanocrystallites obtained experimentally are mixture of anatase and rutile, the uniform diameters of particles are about 30 nm. The phase transformation from anatase to rutile was accelerated by AlCl3, and rutile content is increased from 26.7 wt pct to 53.6 wt pct with increasing of addition of AlCl3 from 0.0 wt pct to 5.0 wt pct. The particle size is reduced and the size distribution becomes very narrow. The crystal lattice constants have the trend to decrease, and celi volumes appear as shrinkable.
文摘Crystal shape distribution, i.e. the multidimensional size distribution of crystals, is of great importance to their down-stream processing such as in filtration as well as to the end-use properties including the dissolution rate and bioavailability for crystalline pharmaceuticals. Engineering crystal shape and shape distribution requires knowledge about the growth behavior of different crystal facets under varied operational conditions e.g. supersaturations. Measurement of the facet growth rates and growth kinetics of static crystals in a crystallizer without stirring has been reported previously. Here attention is given to study on real-time characterization of the 3D facet growth behavior of crystals in a stirred tank where crystals are constantly moving and rotating. The measurement technique is stereo imaging and the crystal shape reconstruction is based on a stereo imaging camera model. By reference to a case study on potash alum crystallization, it is demonstrated that the crystal size and shape distributions (CSSD) of moving and rotating potash alum crystals in the solution can be reconstructed. The moving window approach was used to correlate 3D face growth kinetics with supersaturation (in the range 0.04 - 0.12) given by an ATR FTIR probe. It revealed that {100} is the fastest growing face, leading to a rapid reduction of its area, while the {111} face has the slowest growth rate, reflected in its area continuously getting larger.
基金Support of the National Natural Science Foundation of China (No. 20671028)the Natural Science Foundation of Hebei Province (No. E2006000172)the Postdoctoral Science Foundation of China (No. 2005038511)
文摘The inhibitory effect of phosphate on the crystal grain growth of nanosized titania during high temperature calcination was investigated. Nanosized titanium dioxide powders prepared by hydrolysis of titanium tetrachloride were soaked in phosphate solutions with different concentrations. The obtained powders calcined at various temperatures were characterized by X-ray diffraction （XRD）, Fourier transform infrared spectroscopy （FTIR）, and X-ray photoelectronic spectroscopy （XPS）. The grain size of the samples without phosphate treatment increased quickly when calcined at high temperatures, while the grain size of the samples with phosphate modification increased slowly when calcined at the same temperature. This phenomenon implies that phosphate treatment plays an important role in inhibiting the crystal grain growth of titania. The possible mechanism of the inhibition effect of phosphate on titania is discussed.
文摘Calcium carbonate, the main component of lime, has been widely used in industry due to its stability and economy. Calcium carbonate has three types of crystalline polymorphism, calcite, aragonite and vaterite, each with different properties. Therefore, the control of crystal polymorphism is required for industrial applications. In addition, the control of crystal size and shape is similarly required for different applications. In this study, the effect of SrCO<sub>3</sub> on the size control of fine aragonite-type calcium carbonate crystals by uniform urea precipitation and the effect of SrCO<sub>3</sub> addition was investigated by adding solid strontium carbonate and dissolved strontium carbonate. The addition of solid strontium carbonate affected the crystal polymorphism and size of the calcium carbonate produced, depending on the properties of the solid particles and the amount of SrCO<sub>3</sub> added. Experiments on the addition of dissolved SrCO<sub>3</sub> showed that the supersaturation formation rate could be controlled to control the crystal polymorphism.
基金funded by National Basic Research Program of China(Grant No.2011CB808901)the Geological Survey Program of the China Geological Survey(Grant No.1212011220921)。
文摘The Panzhihua layered intrusions is generated closely related to the Emeishan LIPs.This paper analyzes the spatial distribution of plagioclase and pyroxene.The quantitative texture analysis of 2209 plagioclase shows that the characteristic length of plagioclase is 0.54 to 0.96 mm,the intercept variation range is large,from-0.67 to 0.96,and the slope is-1.85 to-1.04,the Aspect Ratio shows from 1.84 to 2.59 and fractal dimension D is 1.908–1.933.The quantitative texture analysis of 2342 pyroxene shows that the characteristic length of pyroxene is 0.38–0.64 mm,the intercept shows from 0.46 to 2.26,The slope ranges from-2.6 to-1.47,the Aspect Ratio value varies from 1.53 to 1.71,the fractal dimension D is 0.93 to 1.13.All the CSDs results of the Panzhihua intrusions indicate that plagioclase and pyroxene form in an open magma system and undergo four replenishment of magma injection.The plagioclase crystals do not grow as the lathlike shape,and the fractal growth leads to complex crystal surface.The plagioclase undergoes deformation compaction during the crystal process,and then is oriented.The pyroxene crystals grow along an approximately triaxial ratio and undergo texture adjustment and small crystal dissolution reabsorption.When all crystals in magma system grows up to 2 mm,the pyroxene undergoes cumulation in the Panzhihua layered intrusions.The plagioclase crystallization time scale is 171.23–304.41 years,representing that the crystallization is the more uniform in central part of the melt.The nucleation density continuously increases during the crystallization process of the magma system.The time scale to reach the final maximum crystal nucleation density is 15.28–58.98 years.
基金financial support of National Nature Science Foundation (21376178)TIDA giant growth plan (2011-XJR13020)+3 种基金Tianjin Science and technology support program (12ZCDZSF06900)Tianjin University of Science and Technology fund for scientific research (20120119)Tianjin education commission program (20130509)Research fund for the doctoral program of higher education of China (20131208120001)
文摘1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was much oversupplied[1].However particles anhydrous sodium sulphate of large size is not adequate to the demand for its
基金support from the China National Petroleum Corporation (CNPC) (2011B-2304-0305)
文摘The effect of crystal size of USY zeolite on the performance of hydro-upgrading catalysts for treating catalytically cracked(FCC) LCO(light cycle oil) was studied.Three W-Ni catalysts supported on USY zeolites with different crystal sizes and Al2O3 were prepared by impregnation method.The catalysts were characterized by XRD and BET methods,and evaluated in a micro-reactor using tetralin as the model compound and in an 100-mL hydrogenation test unit using FCC LCO as the feedstock.By contrast,catalyst made from smaller crystal-size USY zeolite had higher external surface area and shorter pore length,having more hydrogenation activity sites and short contact time of reactant molecules with acidity sites.The evaluation results showed that the catalyst prepared on the basis of small crystal-size USY zeolite had higher tetralin conversion and better hydro-upgrading performance for treating FCC LCO.
文摘The crystal size distribution（CSD）was determined with small angle X-ray scattering technique.Theanticoking property of Ni-catalysts was investigated with the steam reforming of n-heptane in a TG-monitoredflow reactor.The results of this study show that the rate of coking on the supported Ni-catalysts depends main-ly on the percentage content of the large size fraction（25-70nm）of Ni-crystallites,and that the dispersion ofNi-crystallites and the anticoking property of the Ni/α-Al<sub>2</sub>O<sub>3</sub> catalysts were promoted obviously by theLa<sub>2</sub>O<sub>3</sub>-modification method.The variation of the Ni-CSD and the anticoking property of the catalysts were fur-ther tested through different periods of hydrothermal treatment.It is found that the content of the largeNi-crystal size fraction and the coking rate pass correspondingly through a maximum.
文摘The size and weight fraction of crystals of pure ice or dimethylsulfoxide (DMSO) in poly(vinyl alcohol) (PVA) gel prepared from a mixed solvent of DMSO/water were determined from melting peaks observed by differential scanning calorimetry (DSC). The depression of the melting point with respect to the equilibrium melting point and the melting enthalpy gave the crystal size and weight fraction, respectively. The sizes were in the range of a few nm to tens of nm, depending on the composition ratio of the mixed solvent (DMSO/water) and the polymer concentration. Based on the weight fraction, the critical condition at which the whole solvent became non-freezable was estimated, and it was found to depend on both the PVA concentration and the DMSO/water ratio. When the solvent was pure water, the critical PVA concentration was as high as 86.4 wt%, while for pure DMSO solvent it was 50.1 wt%.
基金Funded by Science Foundation for the Excellent Youth Scholars of Shanghai (No.gjd10028)
文摘A dynamic explicit finite element code and rate-dependent elastic-viscoplastic polycrystalline model were used to simulate the simple tension test of annealing FCC polycrystal and 6111-T4 aluminum alloy sheet metal. The variability of flow stress was investigated, which was induced by various grain boundary constraints when the ratio of thickness-to-grain size was changed. The simulated results show that, when the relative grain size increases, the constraint of grain boundary will increase accordingly, which results in the increase of the flow stress of polycrystal. The results agree with experiments.
