Effects of Calcium Oxide on Physicochemical Properties of Spray-dried Bayberry Powder

[Objective] Effects of different contents of calcium oxide on physicochemi- cal properties of spray-dried bayberry powder were studied. [Method] Bayberry pow- der produced from bayberry juice adding 0, 2 and 4 g/L calcium oxide using the spray drying technique has been selected. The physicochemical properties of the spray-dried bayberry powder were investigated by determining moisture content, colour, apparent density, wettability, angle of repose and moisture absorption rate of bayberry powder. [Result] The results showed that the content of calcium oxide had a significant effect on the moisture content and colour of bayberry powder. Effects of different contents of calcium oxide on the apparent density of spray-dried bayber- ry powder were not obvious. Adding calcium oxide had a significant effect on the wettability, angle of repose and moisture absorption rate of spray-dried bayberry powder, nevertheless, there was not obvious difference on these properties between adding 2 and 4 g/L calcium oxide. [Conclusion] The results confirmed that the con- tent of calcium oxide had a significant effect on the properties of spray-dried bay- berry powder.

PREPARATION OF NANOSIZED METAL-OXIDE ULTRAFINE POWDERS BY ATOMIZING-COMBUSTION TECHNIQUE

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Preparation of low-oxygen-containing Ti-48Al-2Cr-2Nb alloy powder by direct reduction of oxides

A high-purity Ti-48Al-2Nb-2Cr alloy powder with an oxygen content as low as 0.0572 wt.%and a particle size of<150μm was produced from a mixture of TiO_(2),Al_(2)O_(3),Nb_(2)O_(5),and Cr_(2)O_(3)powders through reduction with magnesium and deoxidation with calcium.The phase and composition of the products were analyzed.The final product mainly includedγ-TiAl and minorα_(2)-Ti_(3)Al phases,and Ti,Al,Cr,and Nb were homogenously distributed in the powder with a mole ratio of 49.73:43.51:2.05:1.98.The reduction and deoxidation mechanisms were investigated by thermodynamic modeling using the HSC Chemistry software and Pandat software based on the Ti alloy database.

Preparing low-oxygen Ti-6Al-4V alloy powder through direct reduction of oxides and its synergistic reaction mechanism

Ti-6Al-4V alloy powder was prepared through a two-step reduction of a mixture of TiO_(2),V_(2)O_(5) and Al_(2)O_(3) in this study.The oxide mixture was first reduced by Mg in MgCl_(2) at 750℃ in argon,where oxygen was reduced to 2.47 wt%from 40.02 wt%.The oxygen content in the final powder was eventually reduced to an extremely low level(0.055 wt%)using calcium at 900℃ in argon,and the final powder had the composition of 90.12 wt%Ti,5.57 wt%Al,and 3.87 wt%V,which meets the standard specification of Ti-6Al-4V(ASTM F1108-09).Between the two reductions,a heat treatment step was designed to help controlling the specific surface area and particle size.The effect of the heat treatment temperature on the morphology,and composition uniformity of the powder was investigated in detail.Heat treatment above 1300℃ attributed to a dense powder with a controlled specific surface area.Thermodynamic modeling and experimental results indicated that onlyα-Ti enriched with Al andβ-Ti enriched with V exist in the final powder,and other possible phases including Al-Mg and Al-V were excluded.This study also offers a triple-step thermochemical process for producing high-purity Ti-based alloy powder.

Hydrogen Reduction:A Novel Method of Synthesizing Ultra-fine Chromic Oxide Powder

The ultra-fine chromic oxide powder was prepared by a novel gas-solid reduction reaction.Na2CrO4 was firstly reduced with hydrogen at 400-600 ℃.The obtained reduction products,mainly the mixture of NaCrO2 and sodium hydroxide（NaOH）,were converted into chromic oxide through hydrolysis followed by calcination.The obtained chromic oxide product was characterized by powder X-ray diffraction（XRD） and SEM.The results show that the hydrolysis process of sodium chromite is the key step and lower reduction temperature helps intensify the hydrolysis process.

Synthesis of La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3-δ) Powder for Solid Oxide Fuel Cell by a Nitrate-Citrate Combustion Route

A nitrate-citrate combustion route to synthesize La0.9Sr0.1Ga0.8Mg0.2O3-σ powder for solid oxide fuel cell application was presented. This route is based on the gelling of nitrate solutions by the addition of citric acid and ammonium hydroxide, followed by an intense combustion process due to an exothermic redox reaction between nitrate and citrate ions. The optimum technical parameters are that the pH value is 5, and the molar ratio of citric acid to the total metallic ion is 1.5:1. X-ray diffraction characterization of calcined gel shows that pure phase was synthesized after calcination at 1400℃for 10 h, and the TEM result shovvs the calcined powder with average particle size is about 150 nm. The grain resistance contributes to the total resistance of sintered peliet below 500℃. The conductivity of the sintered peliet at 800℃ was 0.07 S-1·cm-1 higher than the conductivity of YSZ (0.05 S-1·cm-1 at 800℃)

Structure-dependent re-dispersibility of graphene oxide powders prepared by fast spray drying

The graphene oxide powder(GOP)obtained from the spray drying process often exhibits poor redispersibility which is considered due to the partial reduction of GO sheets.The reduction of drying temperature can effectively increase the redispersibility of GOP,but result in a decreased drying efficiency.Herein,we found that the redispersibility of GOP is strongly affected by its microstructure,which is determined by the feed concentration.With the increase of feed concentration,the GO nanosheet assembly varies from the disordered stacking to relatively oriented assembly,making the morphology of the GOP transform from balllike(the most crumpled one)to flakelike(the least crumpled one),and the 0.8 mgml 1 is the threshold concentration for the morphology,structure,and redispersibility change.Once the feed concentration reaches 0.8 mg ml 1,the appearance of the nematic phase in droplet ensures the relatively oriented assembly of GO sheets to form the layered structure with a low crumpling degree,which greatly improves the polar parts surface tension of the solid GOP,making the GOP easier to form hydrogen bonding with water during the redispersion process,thus stabilizing dispersion.This work provides useful information for understanding the relationships between the morphology,microstructure,and final redispersibility of GOPs.

Buckling analysis of embedded graphene oxide powder-reinforced nanocomposite shells

In this study,the buckling analysis of a Graphene oxide powder reinforced(GOPR)nanocomposite shell is investigated.The effective material properties of the nanocomposite are estimated through Halpin-Tsai micromechanical scheme.Three distribution types of GOPs are considered,namely uniform,X and O.Also,a first-order shear deformation shell theory is incorporated with the principle of virtual work to derive the governing differential equations of the problem.The governing equations are solved via Galerkin’s method,which is a powerful analytical method for static and dynamic problems.Comparison study is performed to verify the present formulation with those of previous data.New results for the buckling load of GOPR nanocomposite shells are presented regarding for different values of circumferential wave number.Besides,the influences of weight fraction of nanofillers,length and radius to thickness ratios and elastic foundation on the critical buckling loads of GOP-reinforced nanocomposite shells are explored.

Improving corrosion resistance of additively manufactured WE43 magnesium alloy by high temperature oxidation for biodegradable applications

Laser powder bed fusion(L-PBF)has been employed to additively manufacture WE43 magnesium(Mg)alloy biodegradable implants,but WE43 L-PBF samples exhibit excessively rapid corrosion.In this work,dense WE43 L-PBF samples were built with the relativity density reaching 99.9%.High temperature oxidation was performed on the L-PBF samples in circulating air via various heating temperatures and holding durations.The oxidation and diffusion at the elevated temperature generated a gradient structure composed of an oxide layer at the surface,a transition layer in the middle and the matrix.The oxide layer consisted of rare earth(RE)oxides,and became dense and thick with increasing the holding duration.The matrix was composed ofα-Mg,RE oxides and Mg_(24)RE_(5) precipitates.The precipitates almost disappeared in the transition layer.Enhanced passivation effect was observed in the samples treated by a suitable high temperature oxidation.The original L-PBF samples lost 40%weight after 3-day immersion in Hank’s solution,and broke into fragments after 7-day immersion.The casted and solution treated samples lost roughly half of the weight after 28-day immersion.The high temperature oxidation samples,which were heated at 525℃ for 8 h,kept the structural integrity,and lost only 6.88%weight after 28-day immersion.The substantially improved corrosion resistance was contributed to the gradient structure at the surface.On one hand,the outmost dense layer of RE oxides isolated the corrosive medium;on the other hand,the transition layer considerably inhibited the corrosion owing to the lack of precipitates.Overall,high temperature oxidation provides an efficient,economic and safe approach to inhibit the corrosion of WE43 L-PBF samples,and has promising prospects for future clinical applications.

EFFECT OF OXIDE LAYER THICKNESS OVER Al AND Al ALLOY POWDERS ON QUALITY OF THEIR EXPLOSIVE COMPACTS

Observations of microstructure of explosive compacts made of Al or Al-Li alloy powders by atomization with water,nitrogen or ultrasoic Ar gas were carried out under optical and scanning electron microscopes.The rsults indicate that super quality explosive compact can only be obtained by powders of which the thickness of the oxide layer is less than 30 nm.

Influence of phase components of tungsten oxide on homogeneity of ultrafine tungsten powder

The influence of phase components of tungsten oxide on homogeneity of ultrafine tungsten powder by conventional hydrogen reduction techniques was studied. Results show that phase components of tungsten oxide play a crucial role on homogeneity of metal tungsten powder; ultrafine and homogeneous tungsten powder can be produced from oxides which consist of only one phase. Due to the different reduction rates (or different reduction paths) of oxide which comprises different phases, the multi phase components tungsten oxide leads to a fine but in homogeneous metal tungsten powder.

Plasma-Chemical Synthesis of Nanosized Powders-Nitrides,Carbides,Oxides,Carbon Nanotubes and Fullerenes

In this article the plasma-chemical synthesis of nanosized powders （nitrides, car- bides, oxides, carbon nanotubes and fullerenes） is reviewed. Nanosized powders - nitrides, carbides, oxides, carbon nanotubes and fullerenes have been successfully produced using different techniques, technological apparatuses and conditions for their plasma-chemical synthesis.

Microstructure Study on Nano-phase Powder of Indium Tin Oxide

hemical co-precipitation method was used to prepare indium tin hydroxide. Indium tin hydroxide has the structure of cubic crystal. The cubic crystal structure transformed to amorphous after heat treatment at 250℃ for 1 h. When the heat treatment temperature was higher than 280℃, the amorphous transformed to cubic crystal structure. After heat treatment at 600℃ for 1 h, the particle size of indium tin oxide is 8～20 nm. The weight ratio of In∶Sn is near 9∶1. Its granule has spherical shape. The dispersity is good.

Photocatalytic Activity of Titanium Dioxide Powder Fabricated from an Anodized Titanium Sheet under Ultra-Violet and Visible Light Irradiation

A commercially pure titanium sheet with titanium carbide (TiC) precipitated in its surface layer was anodized in NH4NO3 aqueous solution and heat treated in air. The photocatalytic activity of titanium dioxide powder collected from the surface of the anodized titanium sheet was evaluated under ultra-violet and visible light irradiation. It showed relatively high photocatalytic activity in 0.1 mol/l potassium iodide solution, which was almost equal to the activity level of TiO2 powder (P-25) manufactured by Degussa Corporation. The better photocatalytic activity under ultra-violet irradiation is considered to be related to the formation of anatase type titanium dioxide. Photocatalytic activity under visible light irradiation was also observed, which was considered to be attributable to impurity doping, (carbon), in the titanium dioxide powder.

Preparation of α-Bi_2O_3 from bismuth powders through low-temperature oxidation

α-Bi2O3 powders were prepared from nanometer Bi powders through low-temperature oxidation at less than 873.15 K. XRD, SEM, TEM and HRTEM were used to characterize the structure and morphology of Bi powders and Bi2O3 particles. Kinetic studies on the bismuth oxidation at low-temperatures were carried out by TGA method. The results show that bismuth beads should be reunited and oxidized to become irregular Bi2O3 powders. The bismuth oxidation follows shrinking core model, and its controlling mechanism varies at different reaction time. Within 0-10 min, the kinetics is controlled by chemical reaction, after that it is controlled by O2 diffusion in the solid α-Bi2O3 layer. The apparent activation energy is determined as 55.19 kJ/mol in liquid-phase oxidation.

A Green and Mild Approach of Synthesis of Highly-Conductive Graphene Film by Zn Reduction of Exfoliated Graphite Oxide

We report a simple and green approach to synthesize reduced graphene oxide （RGO） nanosheets at room temperature based on Zn reduction of exfoliated GO. The evolution of GO to RGO has been characterized by X-ray diffraction, UV-Vis absorption spectroscopy and Raman spectroscopy. The results of X-ray photoelectron spectroscopy reveal that the atomic ratio of carbon to oxygen in the RGO can be tuned from 1.67 to 13.7 through controlling the reduction time. Moreover, the conductivity of the RGO is measured to be 26.9±2.2 kS/m, much larger than those previously obtained by chemical reduction through other reducing agents. More importantly, the resistance of the RGO film with 20 nm thickhess can be as low as 2 kΩ/square, while a high transparency over 70% within a broad spectral range from 0.45 pm to 1.50 p.m can be retained. The proposed method is low-cost, eco-friendly and highly-eiffcient, the as-prepared thinner RGO films are useful in a variety of potential application fields such as optoelectronics, photovoltaics and electrochemistry by serving as an ultralight, flexible and transparent electrode material.

Crystal growth of tungsten during hydrogen reduction of tungsten oxide at high temperature

Crystal growth of tungsten during hydrogen reduction of tungsten oxide (WO3) to prepare coarse grain tungsten powder at high temperature (950 ℃) was studied. The phase composition and morphologies of products were investigated by means of XRD and SEM. The results show that the reduction sequence of hydrogen reduction of WO3 is WO3→WO2.9→W18O49→WO2→W. The step of WO2→W is the critical step which determines the grain size of tungsten powder. The partial pressure (pH2O/pH2) of H2O within powder layer shows strong effect on the nucleation and grain growth of tungsten. By increasing the pH2O/pH2 within powder layer, well-developed coarse grain tungsten powder with particle size above 15 μm is obtained. After carburizing, the powder can be used to produce ultra-coarse grain cemented carbide with grain size above 5 μm.

Effects of surface oxide species and contents on SiC slurry viscosity

The disadvantageous effects of colloidal SiO2 layer and micro-content of metal oxide adsorbed on SiC powder surface on SiC slurry stable dispersion were studied, and the novel method to avoid this disadvantage was proposed. By acidwashing, on the one hand, because the maximum Zeta potential of SiC powder increases to 72.49 mV with the decreasing content of metal oxide adsorbed on the SiC powder surface, the repulsion force between SiC powders that dispersed in slurry is enhanced, thus the SiC powder can be fully dispersed in slurry. On the other hand, after HF acidwashing, with the OH^- group adsorbed on SiC powder surface destroyed and replaced by the Fion, the hydrogen bond adsorbed on the OHgroup is also destroyed. Therefore, the surface property of the SiC powder is changed from hydrophilic to hydrophobic; H2O that adsorbed on SiC powder surface is released and can flow freely, and it actually increases the content of the effective flow phase in the slurry. These changes of SiC powder surface property can be proved by XPS and FTIR analysis. Finally, the viscosity of SiC slurry is decreased greatly, and when the viscosity of the slurry is lower than 1 Pa·s, the solid volume fraction of SiC powder in the slurry is maximized to 61.5 vol.%.

Preparation of Arsenic Oxide and High Purity Ultrafine Antimony Compounds from Flue Dust Containing Arsenic and Antimony

A new hydrometallurgical process of chlorination-distillation at low temperatures about 100 °C was developed for recovery of valuable metal and environmental protection. This process was used to treat flue dust containing arsenic and antimony and satisfactory results were obtained. Over 99% of arsenic and antimony were recovered, and high purity As2O3 and SbCl3 were produced. A metallic alcoholate technique was developed and proved to be of significant to the utilization of antimony resources. Using this technique, a number of antimony oxide powders were prepared, such as high purity and ultrafine Sb2O3, ultrafine Sb2O3-Sb2O5 and Sb2O3-SnO2 composite powders.

Mechanochemical Reaction of Lanthanum Carbonate with Sodium Hydroxide and Preparation of Lanthanum Oxide Nanoparticle

The preparation of nano sized La 2O 3 powder by mechanochemical reaction of lanthanum carbonate with sodium hydroxide and subsequent heat treatment was studied using X ray diffraction, differential thermal and thermo gravimetric analysis and transmission electron microscopy. It was found that the mechanochemical reaction process can be divided into two steps: the first step is the multi phases mechanochemical reaction of lanthanum carbonate with NaOH to form amorphous lanthanum basic carbonate and lanthanum hydroxide, and the second step is the crystallization of basic lanthanum carbonate with the formula of La 2(OH) 2(CO 3) 2·H 2O under a quasi hydrothermal synthesis condition caused by the mechanical ball milling. The synthesized La 2O 3 powder appears clearly separated spherical like monodisperse nano size particles in which particle size ranges from 30 to 50 nm.