Phase Analysis of Titanium in Steel and Some Aspects on Their Application

Phase analysis of titanium in steel has been carried out on thirty samples with different Ticontent from 0. 036 %-0. 204% . The various heat treatments for the samples are to anneal at 1050-1200 ℃ for a while ,followed by cooling at a rate of 1 . 10, 20 ℃/s ,respectively.It is achieved to separate and determine fine particle TiC ,coarse particle Ti_2CS and TiN ex-tracted from steel by controlling the oxidation potential and acidity of solutions.The results of quantrtative analysis of the individual phase show that 0. 09 %- 0. 13 % Ti-contentis enough to eliminate free nitrogen and transform MnS into Yi_2CS in steel effectively. In the case of0. 06 %- 0. 10 % Ti-content combined with annealing at 1050℃. and quick cooling at 20 ℃/s ,a prop-er amount of fine particle TiC can be precipitated and the rate of TiC (fine )/TiC (total )is high ,which arebeneficial to increase strength and toughness of steel. More Ti-content or cooling slowly will preciprtatemore coarse particle TiC which decreaces toughness severely. The proposed methods for quantitativephase analysis of titanium in steel are given in detail.

Precipitation of metal oxide nanoparticles using a miniemulsion technique

A method to precipitate nanoparticles using a miniemulsion technique is described, in which miniemulsion droplets between 100 and 1000 nm in size serve as nanoreactors enabling both the control of particle formation and particle growth. The application of miniemulsion droplets to synthesise nanoparticles comprises three advantages： first, the size of the precipitated particles is limited by the reactant concentration within the emulsion droplet; second, particle agglomeration is prevented as nanoparticle collision outside the nanoreactor is avoided; and third, easy technical scale up can be realized by increasing emulsion volume and thus the number of nanoreactors, while local conditions within the reactors are not changed, The miniemulsion technique is an easy scalable process which allows defined synthesis of particles by precipitation reactions. The miniemulsion technique involves first the preparation of a stable water-in- oil miniemulsion by high pressure homogenisation. Whereas a water soluble reactant is provided within the aqueous droplets, another oilas well as water-soluble reactant can be introduced to the emulsion after homogenisation. The precipitation reaction is induced by the diffusion of the second reactant into the emulsion droplet. Together with this contribution, a method is described and discussed which uses a high pressure homogenisation process to produce stable water-in-oil miniemulsions serving as a reaction medium to precipitate metal oxides.

Effect of Intergranular Precipitation on the Internal Oxidation Behavior of Cr–Mn–N Austenitic Stainless Steels

The effect of intergranular precipitation on the internal oxidation behavior of Cr–Mn–N austenitic steels at 1000 °C in dry air atmosphere was investigated using scanning electron microscope, transmission electron microscope, and X-ray diffraction analysis. The results show that intergranular M23C6 carbide morphologies play an important role on the internal oxidation behavior of Cr–Mn–N steels. During the period of the oxidation, both discontinuous chain-shaped and continuous film-shaped intergranular M23C6 carbides precipitated along the grain boundaries. Internal oxides of silica preferentially intruded into the matrix along grain boundaries with discontinuous M23C6 carbide particles, while silica was obviously restricted at the interfaces between the external scale and matrix on the occasion of continuous film-shaped M23C6 carbides. It is seemed that reasonable microstructure could improve the oxidation resistance of Cr–Mn–N steels.

Highly inhibited transport of dissolved thallium(I) in manganese oxide-coated sand: Chemical condition effects and retention mechanisms

Thallium contamination in water can cause great danger to the environment.In this study,we synthesized manganese oxide-coated sand(MOCS)and investigated the transport and retention behaviors of Tl(I)in MOCS under different conditions.Characterization methods combined with a two-site nonequilibrium transport model were applied to explore the retentionmechanisms.The results showed that Tl(I)mobility was strongly inhibited in MOCS media,and the retention capacity calculated from the fitted model was 510.41 mg/g under neutral conditions.The retention process included adsorption and oxidative precipitation by the manganese oxides coated on the sand surface.Cotransport with the same concentration of Mn(II)led to halving Tl(I)retention due to competition for reactive sites.Enhanced Tl(I)retention was observed under alkaline conditions,as increasing pH promoted electronegativity on the media surface.Moreover,the competitive cation Ca^(2+)significantly weakened Tl(I)retention by occupying adsorption sites.These findings provide new insights into understanding Tl(I)transport behavior in water-saturated porous media and suggest that manganese oxide-coated sand can be a cost-effective filter media for treating Tl-contaminated water.

The origin of different morphology of internal oxide precipitates in ferritic and austenitic steels

The internal oxide precipitates were supposed to be spherical in Wagner’s original theory,while the fol-lowing research demonstrated that this assumption is an exception rather than the truth,which caused deviations in the application of this theory.In this study,the internal oxide precipitates have a needle-like and a near-spherical morphology in a Fe-9Cr ferritic and a Fe-17Cr-9Ni austenitic steels after expo-sure to 600℃ deaerated steam for 600 h,respectively.The nano-to-atomic scale characterization shows that the morphology of the internal oxide precipitates is controlled by the structure of the interfaces be-tween the metal matrix and the internal oxide,while the interface structure is mainly affected by the crystallographic structure of the two phases and their orientation relationship.In addition,the internal oxide precipitation-induced volume expansion and the outward Fe diffusion-induced volume shrink oc-cur simultaneously during the oxidation process.The stress status in the internal oxidation zone(IOZ)is the competing result of the two factors,which could dynamically affect the high-temperature oxidation.The results obtained in this study suggest that there is potential to control the distribution,morphology,and interface structure of the internal oxide precipitates by selecting appropriate base metal and internal oxide-forming element,in order to obtain better high-temperature oxidation-resistant materials.

Effect of Temperature on Scale Morphology of Fe-1.5Si Alloy

Because of the effect of silicon on the formation of oxide scale, red scale is the main surface defect of hot rolled Fe-Si plate, making the scale difficult for descaling compared with carbon steel. Thermogravimetric analyzer （TGA） is used to simulate isothermal oxidation process of Fe-1.5Si alloy for 60 min under air condition, and the temperature range is from 700 to 1 200 ℃. Electron probe microanalysis （EPMA） is used to observe cross-sectional scale morphology and analyze elemental distribution of the scale. Relational graph of temperature, scale thickness and scale structure is obtained. It is found that scale structure （outer Fe oxide layer＋inner FeO/Fe2SiO4 layer＋internal Si oxide precipitates） is almost unchanged with temperature except at 1000 and 1 200 ℃. At 1000 ℃ internal Si ox- ide precipitates cannot be found at the subsurface of the alloy, and at 1200 ℃ FeO/Fe2SiO4 not only forms a layer as usual but also penetrates into the outer Fe oxide layer deeply.

Effect of Ce doping of TiO_2 support on NH_3-SCR activity over V_2O_5–WO_3/CeO_2–TiO_2 catalyst

CeO2–TiO2composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5–WO3/CeO2–TiO2catalysts for the selective catalytic reduction（SCR） of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV–Vis,Raman and XPS techniques. The results showed that the catalytic activity of V2O5–WO3/TiO2 was greatly enhanced by Ce doping（molar ratio of Ce/Ti = 1/10） in the TiO2 support.The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning.