Dissolution improvement of fenofibrate by melting inclusion in mesoporous silica

In this study,using mesoporous silica for the solubility enhancement of poorly watersoluble drug was investigated.Although the incorporating drug into mesoporous silica is generally performed through the solvent method,the new melting method was proposed in the present study.Fenofibrate,a poorly water-soluble drug,was incorporated into mesoporous silica by solvent method and melting method.The obtained samples were observed by SEM and their physicochemical properties were evaluated by PXRD and DSC measurement.The dissolution and supersaturated property were also investigated.The results from SEM,PXRD and DSC measurement showed that drug could be loaded into pore via the melting method as well as by the solvent method.The drug loaded quantity depended on the pore volume.Drug up to 33%could be incorporated into mesoporous silica and existed in amorphous state.When drug was overloaded or difficulty in incorporation into pore was found,recrystallization of drug occurred at the outer surface of mesoporous silica.From the dissolution test,samples prepared by solvent method and melting method gave the supersaturated drug concentration which sample from melting method showed superior dissolution to the one from solvent method.From this study,drug was efficiently incorporated into mesoporous silica by the melting method which is a simple and solvent-free process,and the aqueous solubility enhancement of poorly watersoluble drug was achieved.

Structural and electrical characterization of Cu_(2)ZnSnS_(4) ingot material grown by melting method

In this work,a Cu_(2)ZnSnS_(4)(CZTS)ingot is grown via a melting method,then cooled;the resulting molten stoichiomet-ric mixture is sealed off in a quartz ampoule under vacuum.The CZTS powder chemical composition analyses are determined us-ing energy dispersive spectroscopy,and revealing the slightly Cu-rich and Zn-poor character of the ingot.Powder X-ray diffrac-tion analysis reveals a crystalline structure with a kesterite phase formation,and a preferred orientation of(112)plane.The lat-tice constants of the a-and c-axes,calculated based on the XRD analyses,are a=5.40Åand c=10.84Å.Based on Hall measure-ments at room temperature,we find that the crystal exhibits p-type conductivity,with a high concentration of 1018 cm^(-3),a res-istivity of 1.7Ωcm,and a mobility of 10.69 cm^(2)V-1s-1.Activation energies are estimated based on an Arrhenius plot of conductiv-ity versus 1/T,for a temperature range of 80-350 K,measuring 35 and 160 meV in low-and high-temperature regimes,respect-ively,which is attributed to complex defects(2CuZn+SnZn)and antisite defects(CuZn),respectively.The observed scattering mech-anisms are attributed to ionized impurities and acoustic phonons at low and high temperatures,respectively.The extracted band-gap is 1.37 eV.

Preparation of Thermosensitive Microcapsules Containing Water Soluble Powder by Melting Dispersion Cooling Method

It was tried to prepare the thermosensitive microcapsules containing the water soluble solid powder by the melting dispersion cooling method and to establish the optimum preparation conditions. As a model water soluble solid powder, sodium hydrogen carbonate was adopted in order to generate carbon dioxide gas and as a thermosensitive shell material, olefin resin with the melting point of ca. 40°C was used. In the experiment, the concentration of olefin resin in the shell material solution was mainly changed together with the concentrations of the oil soluble surfactant species and the α-tocopherol as a modifier of shell. Addition of α-tocopherol into the shell material solution could prevent the core from breaking away during the microencapsulation process and result in the higher microencapsulation efficiency, because the dispersion stability of solid powder in the shell material solution could be increased due to the increase in affinity between the shell material solution and solid powder. Also, the microencapsulation efficiency increased with the concentration of olefin resin, became maximum at 50 wt% and then, decreased. The microcapsules were found to begin melting at 36°C and to generate carbon dioxide gas.

Effects of porosity and pore size on the compressive properties of closed-cell Mg alloy foam

In our current work,AZ31 magnesium alloy foams with closed-cell were successfully fabricated by melt foaming method using Ca and CaCO3 as thickening and blowing agent,respectively.The influences of porosity and pore size on the quasi-static compressive properties of the foams were systematically investigated.The results showed that the yield strength,energy absorption capacity and ideality energy absorption efficiency were decreased with the increase in porosity.However,specimens with porosities of 60%,65%and 70%possessed similar total energy absorption capacity and ideality energy absorption efficiency.Meanwhile,experimental results showed that mean plateau strength of the foams was increased first and then decreased with increase in mean pore size.In addition,energy absorption capacities were almost the same in the initial stage,while the differences were obvious in the middle stage.From the engineering point of view,the specimens with mean pore size of 1.5 mm possess good combination of mean plateau strength and energy absorption characteristics under the present conditions.

区熔法生长近化学计量比铌酸锂晶体

The congruently melting composition of Lithium Niobate(LN) is 48.6mol% Li 2O,rather than stoichiometric 50mol%Li 2O.By means of conventional Czochralski(CZ) method,it is easy to grow the congruent LN crystal with high quality,but difficult to grow the stoichiometric LN crystal with homogeneous composition. In contrast to CZ method,Melting Zone(MZ) method makes use of the segregation of solute,and is likely to grow homogeneous crystal.By MZ method,we have grown near stoichiometric LN crystal (Li%mol=49.5%) from stoichiometric LN raw material. The difference between the raw material and the crystal is due to the volatilization loss of Lithium at the growing temperature.With 50.5mol%Li 2O LN raw material,stoichiometric LN crystal could be grown. Li rich LN solvent zone preplaced in the melting zone makes the crystal much more homogeneous than that without the solvent zone.The preplaced Li rich zone heightens the starting [Li] concentration of the liquid phase,so that the initial [Li] concentration of LN crystal is close to the stable value,and the process of stabilization is shortened.

Electrochemical impedance spectra of V_2O_5 xerogel films with intercalation of lithium ion

Vanadium pentoxide xerogel films used for lithium rechargeable batteries were prepared from crystalline c-V2O5 by melt quenching method,then the electrochemical process of lithium intercalation into vanadium pentoxide xerogel films was simulated with an equivalent circuit model, which was derived from the mechanism of electrode reactions. Measured electrochemical impedance spectra at various electrode potentials were analyzed by using the complex non-linear least-squares fitting method. The results show that impedance spectra consist of 2 high-to- medium frequency depressed arcs and a low frequency straight line. The high frequency arc is attributed to the absorption reaction of lithium ions into the oxide film, the medium frequency arc is attributed to the charge transfer reaction at the vanadium oxide/electrolyte interface and the low frequency is characterized by a straight line with a phase angle of 45° corresponding to the diffusion of lithium ion through vanadium oxide phase. The experimental and calculated results are compared and discussed focusing on the electrochemical performance and the state of charge of the electrode. Moreover, the high consistence of the fitted values of the model to the experimental data indicates that this mathematical model does give a satisfying description of the intercalation process of vanadium pentoxide xerogel films.

Production technique of vermicular graphite iron cylinder head of vehicle diesel engine

The 25 years＇ production and application have proved that vermicular graphite iron cylinder heads with vermicularity ≥50% satisfy the machinability and performance demand of diesel engine. The method, in which using cupola-induction furnace duplex melting and pour-over process with rare earth-ferrosilicon or rare earthsilicon compound as vermJcularizing alloy plus rare earth-magnesium-ferrosilicon as stirring alloy, is an optimal vermicularizing process for obtaining satisfied vermicularity. Using top kiss risers, enlarging kissing areas and expanding covering width and making ingates to freeze earlier are the effective measures to eliminate shrinkage, blowhole and oxide inclusions in the vermicular graphite iron cylinder heads.

Microstructure and Electrochemical Characteristics of Melt-Spinning Alloy Ml(NiCoMnAl)_5

The microstructure and electrochemical characteristics of Ml(NiCoMnAl) 5 alloys prepared by both the melt spinning method and the conventional induction melting were investigated and compared. SEM and XRD studies show that the microstructure of melt spinning alloys is columnar structure. With increasing melt spinning rate, the crystal grains become finer and preferentially grow along (111)[111] direction. The melt spinning and cast alloys belong to CaCu 5 type hexagonal crystal structure. The electrochemical measurements show that the initial capacities of melt spinning alloy electrodes are all above 210 mAh·g -1 with good activation behavior, reaching their maximum capacities after two charge discharge cycles. The maximum capacity (294 mAh·g -1 ) of melt spinning (10 m·s -1 ) alloy electrodes is as the same as that of as cast alloy electrode, and stability of charge discharge cycles of all melt spinning alloy electrodes is better than that of the as cast alloy electrodes. When charged at 600 mA·g -1 , the capacity of melt spinning (10 m·s -1 ) alloy electrode could reach 65% of its maximum capacity about 45 min with high rate discharge capability; but with the cycle number increasing, the stability of its capacity is less than that electrodes of melt spinning rate.

Effects of melt spinning process parameters and wheel surface quality on production of 6060 aluminum alloy powders and ribbons

The aim of this study is to investigate the surface quality of the melt spinning wheel, which was changed from smooth type to textured structure, to atomize liquid metal to form powders. The effects of melt spinning process parameters like wheel speed, gas ejection pressure, molten metal temperature, nozzle–wheel gap and wheel surface quality on the morphological and microstructural features of 6060 aluminum alloy powders and ribbons were investigated. It was observed that ribbon type material was obtained with the smooth wheel and the powder was produced with textured type. The sizes of produced ribbons with smooth surface wheel varied in the range of 30-170 μm in thickness, 4-8 mm in width, and 0.5-1 m in length. The average powder size of the powders manufactured using the textured wheel was in the range of 161-274 μm, depending on the process parameters.Increasing the wheel speed, melt temperature and decreasing gas ejection pressure, nozzle-wheel gap resulted in the decrease of both ribbon thickness and powder size. The microstructures of the powders and ribbons were the equiaxed cellular type, and the average grain sizes diminished with decreasing the ribbon thickness and powder size. The maximum cooling rates were 2.00×10^5 and 1.26×10^4 K/s for the ribbon with thickness of 30 μm and for the powder with size of 87 μm, respectively.

Compressive characteristics of closed-cell aluminum foams with different percentages of Er element

In the present study, closed-cell aluminum foams with different percentages of erbium （Er） element were successfully prepared. The distribution and existence form of erbium （Er） element and its effect on the compressive properties of the foams were investigated. Results show that Er uniformly distributes in the cell walls in the forms of Al3Er intermetallic compound and AI-Er solid solutions. Compared with commercially pure aluminum foam, Er-containing foams possess higher micro-hardness, compressive strength and energy absorption capacity due to solid solution strengthening and second phase strengthening effects. Additionally, the amount of Er element should be controlled in the range of 0.10wt.%-0.50wt.% in order to obtain a good combination of compressive strength and energy absorption properties.

Investigation on the Tensile Properties and Fracture Characteristics of Amorphous Ribbons Fe81.50B1.40Si7.95Nb7.37Cu1.73P0.05

A number of Fe-Si-B amorphous ribbons are made by using melt spinning method. The microstructure, mechanical and other relevant properties of thin amorphous ribbons of Fe81.50B1.40Si7.95Nb7.37Cu1.73P0.05 alloy at room temperature were studied with several equipment including Differential scanning calorimetry (DSC), X-ray diffraction (XRD),Scanning electron microscope (SEM), and tensile machine. Significantly different microstructures exist between the free and wheel face of the thin amorphous ribbons. The free face is smooth while the wheel face is coarse with a great number of micro voids on the surface. Experimental results show that the tensile strength and elastic modulus of thethin amorphous ribbons at room temperature are 1951 MPa and 70 GPa. In addition, the amorphous ribbons possess reasonable tensile elongation (2.46%). The fracture appearance of amorphous ribbons of Fe81.50B1.40Si7.95Nb7.37Cu1.73P0.05 alloyis a mixed mode of ductile and brittle fracture which includes dimples and partial cleavage fracture similar to the crystalline materials. The dimple feature proves that it still has plastic characteristics on the micro scale.

Superelasticity of Cu–Ni–Al shape-memory fibers prepared by melt extraction technique

In the paper, a melt extraction method was used to fabricate Cu–4Ni–14Al（wt%） fiber materials with diameters between 50 and 200 μm. The fibers exhibited superelasticity and temperature-induced martensitic transformation. The microstructures and superelasticity behavior of the fibers were studied via scanning electron microscopy（SEM） and a dynamic mechanical analyzer（DMA）, respectively. Appropriate heat treatment further improves the plasticity of Cu-based alloys. The serration behavior observed during the loading process is due to the multiple martensite phase transformation.

Organic Melt Crystallization as a Method for Synthesis of Supramolecular Complexes

The most simple method for solventless synthesis of supramolecular complex of CMCR·2BPY·BZP, [CMCR = C-methylcalix[4]resorcinarene, BPY = 4,4'-bipyridine, BZP = benzophenone], is proposed. Although CMCR by itself is high melting point compound (above 300°C), CMCR was found to be dissolved in melt mixture of BPY and BZPeven below 120°C. In the mixture of the three components, the reaction occurs to form CMCR·2BPY·BZP supramolecular complex.