Synthesization and crystallization mechanism of nano-scale γ-AlOOH with various morphologies

Nano-scale γ-AIOOH with various morphologies, such as whisker, bar, ball, and sheet, was synthesized successfully and control- lably through a facile hydrothermal method just by adjusting the pH value of the solvent. Based on the analysis of the experimental data, the growth mechanism of nano-scale γ-AlOOH in the hydrothermal process was established. It is proposed that the growth unit and the growth direction are determined by the pH value of the solution and the growth unit, respectively. One-dimensional γ-AlOOH, such as whisker and bar, is formed in lower pH ranges, while two-dimensional γ-AlOOH sueli as sheet is formed only in high pH environment following the plane expansion crystallization mechanism.

Influence of Nano-Nd_2O_3 on Crystallization Mechanism of Fused Quartz

The isothermal crystallization kinetics of pure fused quartz of blank specimen N- 0 and specimen N- 3 in troduced with 3 mass% nano-Nd2O3 was researched by means of XRD and Avrami equation. The results show that crystallization mechanisms of fused quartz in two specimens are both heterogeneous nucleation type caused by surface structure defects,and the grain growth mode of two specimens are both two-dimensional growth ac companied by one-dimensional and three-dimensiona growths,specimen N- 3 has the higher degree of grain growth in one-dimensional and three-dimensional than specimen N- 0; introducing nano-Nd2O3 can obviously reduce the ＂active nucleation sites＂of glass structure on the fused quartz particles surface,enhance the stability o glass structure,increase the activation energy of fused quartz crystallization from 874 k J · mol- 1to 1 270 k J·mol- 1,and decrease the crystallization rate of fused quartz obviously.

A study of the crystallization kinetics of Ge-Te amorphous systems

The glass-forming ability of binary GexTe100-x (x=15, 20, 30) alloys was investigated. The crystallization mechanism of these amorphous bulks was studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and differential scanning calo- rimetry (DSC). The temperature of glass transition, the temperature of crystallization, the activation energy for glass transition and crystallization, and the order of the crystallization mechanism were calculated from the different heating-rates.

Effect of pH on Crystallization of Nanocrystalline Zirconia in a Microwave-hydrothermal Process

Nanocrystalline zirconia（ZrO） was synthesized using a microwave-hydrothermal process.The effect of pH on the crystallization of the ZrO2 powders was investigated.The phase and microstructure of ZrO2 powders were examined using X-ray diffraction（XRD）,Raman spectroscopy,and transmission electron microscopy（TEM）.Results show that pure m-ZrO2 can be obtained at low pH（pH＆lt;2）.Pure t-ZrO2 is formed at pH = 7 and 14.The size of the ZrO2 crystals is in the range of 8-26 nm and decreases with increasing pH.The formation of m-ZrO2 results from the precipitation of ZrO2 from solution.The t-ZrO2 is formed through the in-situ structural rearrangement of amorphous Zr（OH）xOy.The stabilization of t-ZrO2 is attributed to the small crystal size and the adsorption of hydroxy ions on the surfaces of the crystals.

Shaped binderless ZSM-11 zeolite catalyst prepared via a dry-gel conversion method:Characterization and application for alkylation of benzene with dimethyl ether

Shaped binderless ZSM-11 zeolite catalysts were synthesized via a dry-gel conversion technique from 70ZSM-11/30 SiO;mix extrudates. 1,6-hexanediamine combined with tetrabutylammonium bromide was proved to be the best structure directing agent for the synthesis of the binderless ZSM-11 catalyst, without adding other alkaline materials. The 70HZSM-11/30 SiO;mix serials materials crystallized for different times were detected by X-ray diffraction（XRD）, nuclear magnetic resonance（NMR）, scanning electron microscopy（SEM）, transmission electron microscopy（TEM）, scanning transmission electron microscopy–energy dispersive spectroscopy（STEM–EDS） techniques, and so on. In order to investigate the possible crystallization mechanism, the textural and structural properties of 70HZSM-11/30 SiO;mix serials samples were further characterized by N;adsorption–desorption. Acid properties were determined by temperature-programed desorption of NH;（NH;-TPD） and pyridine adsorption-infrared（Py-IR） measurements. In the alkylation of benzene with dimethyl ether, the serials catalysts exhibited different benzene conversions. 70HZSM-11/30 SiO;mix showed the lowest benzene conversion while sample 70HZSM-11/30 SiO;mix-6.5h synthesized only for 6.5h displayed a higher benzene conversion, even higher than the value over 70HZSM-11/30Al;O;mix. Extending the crystallization time, the obtained samples displayed the increased benzene conversion in general under the same reaction conditions. In the end, the relation of physicochemical properties with the reaction performance was investigated.

A Critical Review on Superchilling Preservation Technology in Aquatic Product

aquatic product, known as one of the good resources for white meat, has been widely accepted by the consumers due to its high protein, low fat, especially low cholesterol. With the fast development of living standards around the world, the consumer demands for high quality, nutrition, safety and freshness of ifshery food are increasing. Thus, high efifcient preservation technologies for aquatic products become particularly important. Superchilling is one of the controlled-temperature preservation technologies for seafood. Aquatic products can be kept in better quality under superchilling conditions. This review introduced the principle and development of superchilling process, mainly focusing on research progresses and technical dififculties of superchilling. The growth mechanism of ice crystals and the feasibility of application of computational lfuid dynamics in analyzing the temperatures variation and ice crystals during superchilling progress were also discussed, which will provide theoretical foundation for its improvement and application.

Synthesis and characterization of copolymers of poly(m-xylylene adipamide) and poly(ethylene terephthalate) oligomers by melt copolycondensation

Poly（m-xylylene adipamide）/poly（ethylene terephthalate）（MXD6/PET） copolymers are synthesized by melt copolycondensation with 1–5 wt% low molecular weight PET oligomers into the MXD6 oligomers at 260 ℃.FR-IR and1 H NMR analysis results indicate that the interchange reaction has occurred between MXD6 oligomers and PET oligomers. The thermal behavior of copolymers shows that the melting temperature of MXD6/PET copolymers decreases with the increasing of amount of PET oligomers, while the crystallization temperature accordingly increases. And the equilibrium temperature Tm0 is evaluated to be 251.8 ℃ for the copolymers with5 wt% PET oligomer adding, which is very close to that of neat MXD6. The tensile and impact strength of MXD6/PET copolymers are significantly improved than that of pure MXD6 by mechanical properties test, and the microfibril structure in the impact fracture sample＇s surface reveals the feature of ductile fracture.

Optical and defect properties of S-doped and Al-doped GaSe crystals

S-doped and Al-doped GaSe crystals are promising materials for their applications in nonlinear frequency conversion devices. The optical and defect properties of pure, S-doped, and Al-doped GaSe crystals were studied by using photoluminescence（PL） and Fourier transform infrared spectroscopy（FT-IR）. The micro-topography of（0001） face of these samples was observed by using scanning electron microscope（SEM） to investigate the influence of the doped defects on the intralayer and interlayer chemical bondings. The doped S or Al atoms form the SSe^0 or AlGa^＋1） substitutional defects in the layer GaSe structure, and the positive center of AlGa-^＋1 could induce defect complexes. The incorporations of S and Al atoms can change the optical and mechanical properties of the GaSe crystal by influencing the chemical bonding of the layer structure. The study results may provide guidance for the crystal growth and further applications of S-doped and Al-doped GaSe crystals.

Mechanical alloying characteristic and thermal stability of Al_(78)Fe_(20)Zr_2 amorphous powders

The powders of pure Al, Fe, and Zr for preparing Al78Fe20Zr2 were subject to a high-energy planetary ball milling.The microstructure evolution of the mixtures at the different intervals of milling was characterized by X-ray diffraction（XRD）, transmission electron microscopy（TEM） and differential scanning calorimetry（DSC）.It was found that a nearly complete amorphization could be achieved in the mixtures after ball milling for 23 h.Further ball milling led to the crystallization of the amorphous powders.A long time ball milling, e.g., 160 h, led to a complete crystallization of the amorphous powders and the formation of Al3Zr and Al13Fe4.The crystallization products caused by ball milling are almost the same as that produced by isothermal annealing of the amorphous powders in vacuum at 800 K for 1 h.

Decoding the nature of interaction between felsic clasts and mafic magma in a subvolcanic magma chamber from amphibole–titanite transformation and chemistry

The Ghansura Rhyolite Dome of Bathani vol-cano-sedimentary sequence,eastern India,represents a subvolcanic felsic magma chamber that was invaded by crystal-rich mafic magma during its cooling phase to form an assortment of hybrid rocks.A prominent solidified portion of the magma reservoir was embedded in the intruding mafic magma as fragments or clasts that pro-duced mafic rocks with felsic clasts.Two distinct compo-sitional zones could be identified in the mafic rocks containing felsic clasts-(a)medium-grained mafic zones that are dominated by amphiboles,and(b)fine-grained felsic zones consisting primarily of quartz and feldspar.Amphiboles occur in most of the felsic clasts suggesting the mechanical transfer of crystals from the mafic to the felsic zones.Compositions of amphiboles were determined from both the mafic and felsic zones that show linear compositional variation from actinolite to ferro-hornblende through magnesio-hornblende,suggesting the interplay of complex substitutions in individual amphibole sites.Cationic schemes have confirmed the role of pargasite(Pg)-type substitution,which is a combination of edenite(Ed)-and tschermakite(Ts)-type substitutions.Moreover,amphibole has been extensively replaced by titanite in the studied rock.Titanite produced in the mafic zones due to the destabilization of amphiboles was observed migrating from the mafic to the felsic zones through mineral-trans-porting veins.Compositions of titanite were determined from grains that occur in association with amphiboles and those which are present as individual entities in the felsic zones.Similar to amphiboles,titanite also displays cationic substitutions in the studied rock.From the results presented in this work,we infer that extensive replacement of amphibole by titanite and cationic substitutions in amphi-boles,and also titanite,may be considered important pet-rogenetic indicators to decipher magma mixing events.

Influence of Temperature on Stacking Fault Energy and Creep Mechanism of a Single Crystal Nickel-based Superalloy

The influence of temperatures on the stacking fault energies and deformation mechanism of a Re- containing single crystal nickel-based superalloy during creep at elevated temperatures was investigated by means of calculating the stacking fault energy of alloy, measuring creep properties and performing contrast analysis of dislocation configuration. The results show that the alloy at 760 ℃ possesses lower stacking fault energy, and the stacking fault of alloy increases with increasing temperature. The defor- mation mechanism of alloy during creep at 760 ℃ is 7＇ phase sheared by 〈110〉 super-dislocations, which may be decomposed to form the configuration of Shockley partials plus super-lattice intrinsic stacking fault, while the deformation mechanism of alloy during creep at 1070 ℃ is the screw or edge super- dislocations shearing into the rafted 7＇ phase. But during creep at 7（50 and 980 ℃, some super- dislocations shearing into 7＇ phase may cross-slip from the {111} to {100} planes to form the K-W locks with non-plane core structure, which may restrain the dislocations slipping to enhance the creep resis- tance of alloy at high temperature. The interaction between the Re and other elements may decrease the diffusion rate of atoms to improve the microstructure stability, which is thought to be the main reason why the K-W locks are to be kept in the Re-containing superalloy during creep at 980 ℃.

Crystal structure of full-length human glucagon receptor reveals novel receptor activation mechanisms

Subject Code:C05With the support by the National Natural Science Foundation of China,a team of scientists let by Profs.Wu Beili(吴蓓丽),Wang Mingwei and Jiang Hualiang from Shanghai Institute of Materia Medica,Chinese Academy of Sciences has determined the high-resolution atomic structure of a full-length class B

Metal-organic frameworks:Synthetic methods for industrial production

Metal-organic frameworks(MOFs),which are constructed by metal ions or clusters with organic ligands,have shown great potential in gas storage and separation,luminescence,catalysis,drug delivery,sensing,so on.More than 20,000 MOFs have been reported by adjusting the composition and reaction conditions,most of them were synthesized by hydrothermal or solvothermal methods.The conventional solvothermal methods are favorable for the slow crystallization of MOFs to obtain single crystals or highly crystalline powders,which are suitable for the structure analysis.However,their harsh synthesis conditions,long reaction time,difficulty in continuous synthesis limit their scale-up in industrial production and application.Meanwhile,shaping or processing is also required to bring MOF crystals and powders into the market.Therefore,this review demonstrates the crystallization mechanisms of MOFs to understand how the synthetic parameters affect the final products.Additionally,a variety of promising synthetic routes which can be used for large scale synthesis were reviewed in details.Lastly,the prospects of MOF shaping and processing are provided to promote their industrial application.

Progress in Seed-assisted Synthesis of (Silico) Aluminophosphate Molecular Sieves

Aluminophosphate(AlPO)and silicoaluminophosphate(SAPO)molecular sieves are an important class of open-framework crystalline materials with wide applications thanks to their molecular-scale selectivity,moderate/strong acidity and excellent(hydro)thermal stability.In recent decades,the manufacturing of new microporous solids with ordered structures has been widely investigated and many effective methods have been developed,which enriches the material types and broadens their applications beyond the traditional use as catalysts and adsorbents.However,the development on the synthesis of AlPO/SAPO molecular sieves is still insufficient and lags behind the needs of applications.Herein,we summarize the work on the seed-assisted synthesis of AlPO/SAPO molecular sieves compared with the zeolite synthetic system,aiming to prompt the synthesis and application of AlPO/SAPO molecular sieves.

Progress in synthesis of highly crystalline covalent organic frameworks and their crystallinity enhancement strategies

Covalent organic frameworks(COFs) have been attracting growing concerns since the first report in2005. With the well-defined and ordered structures, COFs express big potential in mass transport, storage/separation and energy conversion applications. From the perspective of both theory and application,the construction of crystalline COFs with high quality and variety is highly worth to be devoted to. To give insight into the crystalline process of COFs and deeply understand the factors of COFs crystallization,this review was concentrated on the recent progress in construction of crystalline COFs. Accordingly, the types and crystallization process of COFs were summarized firstly. And then the factors on crystallinity and the measures for improving the crystallinity of COFs were classified and discussed in detail. Finally,the perspectives for the development of COFs in further was given at the end of this review.

Coarsening Behavior of Gamma Prime Precipitates in a Nickel Based Single Crystal Superalloy

The γ/γ＇ microstructural evolution in a nickel based single crystal superalloy during load-free thermal exposure at 900 ℃ has been further investigated in this paper. The growth characteristics of γ＇ precipitates were discussed in detail. The generation of interfacial dislocations would accelerate the rate of coalescence in the dendrite arms. The average sizes of precipitates were used to compare interface with diffusion controlled growth mechanism and no mechanism seems obviously dominant, although the square rate law gives slightly better fit. The coarsening behavior may be controlled by diffusion through the ragged interface between the γ＇ precipitate and the y matrix.

A 150%enhancement of PMOSFET mobility using hybrid orientation

A high-performance PMOSFET based on silicon material of hybrid orientation is obtained.Hybrid orientation wafers,integrated by（100） and（110） crystal orientation,are fabricated using silicon-silicon bonding, chemical mechanical polishing,etching silicon and non-selective expitaxy.A PMOSFET with W/L = 50μm/8μm is also processed,and the measured results show that the drain-source current and peak mobility of the PMOSFET are enhanced by up to 50.7%and 150%at V_（gs） =-15 V and V_（ds） =-0.5 V,respectively.The mobility values are higher than that reported in the literature.

High Temperature Stress Rupture Anisotropy of a Ni-Based Single Crystal Superalloy

High temperature stress rupture anisotropies of a second generation Ni-base single crystal（SC） superalloy specimens with [001], [011] and [111] orientations under 900 ℃/445 MPa and 1100 ℃/100 MPa have been investigated in the present study, with attentions to the evolution of γ/γ′ microstructure observed by scanning electron microscopy and the dislocation configuration characterized by transmission electron microscopy in each oriented specimen. At 1100 ℃/100 MPa as well as 900 ℃/445 MPa, the single crystal superalloy exhibits obvious stress rupture anisotropic behavior. The [001] oriented specimen has the longest rupture lifetime at 900 ℃/445 MPa, and the [111] oriented sample shows the best rupture strength at 1100 ℃/100 MPa. While the [011] oriented specimen presents the worst rupture lifetime at each testing condition, its stress rupture property at 1100 ℃/100 MPa is clearly improved, compared with900 ℃/445 MPa. The evident stress rupture anisotropy at 900 ℃/445 MPa is mainly attributed to the distinctive movement way of dislocations in each oriented sample. Whereas, at 1100 ℃/100 MPa, together with the individual dislocation configuration, the evolution of γ/γ′ microstructure in each orientation also plays a key role in the apparent stress rupture anisotropy.

Ultra-wide tuning single channel filter based on one-dimensional photonic crystal with an air cavity

By inserting an air cavity into a one-dimensional photonic crystal of LiF/GaSb, a tunable filter covering the whole visible range is proposed. Following consideration of the dispersion of the materials, through modulating the thickness of the air cavity, we demonstrate that a single resonant peak can shift from 416.1 to 667.3 nm in the band gap at normal incidence by means of the transfer matrix method. The research also shows that the transmittance of the channel can be maximized when the number of periodic Li F/Ga Sb layers on one side of the air defect layer is equal to that of the other side. When adding a period to both sides respectively, the full width at half maximum of the defect mode is reduced by one order of magnitude. This structure will provide a promising approach to fabricate practical tunable filters in the visible region with ultra-wide tuning range.

Investigation of Structural, Electronic and Mechanical Properties of Rubidium Metal Hydrides RbMH_4(M=B, Al, Ga)

Ab initio calculations are performed to investigate the structural stability, electronic structure and mechanical properties of rubidium metal hydrides RbMH4（M = B, Al, Ga） for five different crystal structures, namely hexagonal（P63mc）, tetragonal（P42/nmc）, tetragonal（P421c）, orthorhombic（Pnma） and monoclinic（P21/c）. Among the considered structures, tetragonal（P421c） phase is found to be the most stable one for these metal hydrides at normal pressure. A pressure-induced structural phase transition from tetragonal（P421c） to monoclinic（P21/c） phase is observed in all the three metal hydrides. The electronic structure reveals that these hydrides are wide band gap semiconductors. The calculated elastic constants indicate that these alkali metal tetrahydrides are mechanically stable at normal pressure.