Aluminizing Low Carbon Steel at Lower Temperatures

This study reports the significantly enhanced aluminizing behaviors of a low carbon steel at temperatures far below the austenitizing temperature, with a nanostructured surface layer produced by surface mechanical attrition treatment （SMAT）. A much thicker iron aluminide compound layer with a much enhanced growth kinetics of η-Fe2Al5 in the SMAT sample has been observed relative to the coarse-grained steel sample. Compared to the coarse-grained sample, a weakened texture is formed in the aluminide layer in the SMAT sample. The aluminizing kinetics is analyzed in terms of promoted difusivity and nucleation frequency in the nanostructured surface layer.

Aluminizing Coating and Aluminizing-Y_2O_3 Coating Deposited by Pulsed Spark

Aluminizing coating and aluminizing-dispersed Y 2O 3 composite coating were prepared on 20 steel specimens by pulsed spark technique, which exhibited a micro-crystallized structure with grain size in the range of several ten to several hundred nanometers. It is shown that, after oxidation at 600 ℃ in air for 100 h, these two kinds of coatings have excellent resistance to high temperature oxidation and scale spallation, and the aluminizing-dispersed Y 2O 3 composite coating has even better property than the aluminizing coating. AFM, SEM, EDS and XRD were applied to analyze the surface morphology, composition and phases structure of these coatings and the oxide scale formed in oxidation. The mechanism for these coatings that how to enhance the oxidation resistance and scale spallation resistance was discussed by considering the factors, such as Al concentration on the selective oxidation of Fe-Al alloy, the effect of micro-crystallization, reactive element effect (REE) caused by dispersed Y 2O 3, etc.

Heat Transfer during the Solidification of Hot Dip Aluminizing Coating

Hot dip aluminizing is one of the most effective methods of surface protection for steels and is gradually gaining popularity.Although the pulling speed is one of the most important parameters to control the coating thickness of aluminizing products,however,there are few publications on the mathematical modeling of pulling speed during the hot dip process.In order to describe the correlation among the pulling speed,coating thickness and solidification time,the principle of mass and heat transfer during the aluminizing process is investigated in this paper.The mathematical models are based on Navier-Stokes equation and heat transfer analysis.Experiments using the self-designed equipment are carried out to validate the mathematical models.Specifically,aluminum melt is purified at 730 ℃.The Cook-Norteman method is used for the pretreatment of Q235 steel plates.The temperature of hot dip aluminizing is set to 690 ℃ and thedipping time is set to 3 min.A direct current motor with stepless speed variation is used to adjust the pulling speed.The temperature change of the coating is recorded by an infrared thermometer,and the coating thickness is measured by using image analysis.The validate experiment results indicate that the coating thickness is proportional to the square root of pulling speed for the Q235 steel plate,and that there is a linear relationship between coating thickness and solidification time when the pulling speed is lower than 0.11 m/s.The prediction of the proposed model fits well with the experimental observations of the coating thickness.

Pack Aluminizing of Copper

Aluminizing of Cu by a pack cementation process was performed to improve its surface properties.The effect of variation of pack aluminizing temperature from 800 to 900℃ and aluminizing time from 1 to 6 h on the microstructure and the thickness of the aluminide coating of Cu was investigated. Pack aluminizing of Cu significantly improved the microhardness and the oxidation resistance. The microhardness was increased about seven times and the oxidation resistance,after 96 h exposure in air at 900℃, was extremely increased ten times by aluminizing Cu at 900℃ for 3 h.

RE-aluminithermic Aluminizing

The steel surface treatment by rare-earth aluminithermic aluminizing,which was utilized onthermal couple,buried parts of lightning arrester and silencer of automobile,has met with success.This new technique was studied by Beijing University of Science and Technology,BeijingIron-steel Institute and Jingdong Work of Corrosion-protective Materials cooperatively.The steel

Corrosion Behavior of Fe–Al Coatings Fabricated by Pack Aluminizing Method

In this study, the two kinds of Fe-Al coatings were fabricated by pack aluminizing on low-carbon steel at different temperatures. The corrosion behavior of the Fe-Al coatings in artificial seawater was investigated by the electrochemical and weight loss techniques. Results show that the thickness of coating layer increases with increasing aluminizing temperature. The coatings exhibit high micro-hardness and good metallurgical bonding with the substrate. In comparison with the steel substrate, the corrosion current density Ico^r of the Fe-AI coatings is always lower than that of substrate, about 1/38 or 1/33 after 2 h immersion, and 1/3 or 1/6 for 720 h immersion. As can be seen from the weight loss curve, the Fe-AI coatings show less loss than that of the substrate within 30-day immersion. The corrosion products formed on the surface of the coatings include oxides of Al, Mg, Fe and Ca, and pitting defect has also been found. The Fe-Al coating with higher content of Fe2Al5 has better corrosion resistance.

Assessing the energy release characteristics during the middle detonation reaction stage of aluminized explosives

Afterburning behind the detonation front of an aluminized explosive releases energy on the millisecond timescale,which prolong the release of detonation energy and the energy release at different stages also shows significant differences.However,at present,there are few effective methods for evaluating the energy release characteristics of the middle reaction stage of such explosives,which can have a duration of tens to hundreds of microseconds.The present work demonstrates an approach to assessing the midstage of an aluminized explosive detonation based on a water push test employing a high degree of confinement.In this method,the explosive is contained in a steel cylinder having one end closed that is installed at the bottom of a transparent water tank.Upon detonation,the gaseous products expand in one direction while forcing water ahead of them.The resulting underwater shock wave and the interface between the gas phase products and the water are tracked using an ultra-high-speed framing and streak camera.The shock wave velocity in water and the expansion work performed by the gaseous detonation products were calculated to assess the energy release characteristics of aluminized explosives such as CL-20 and RDX in the middle stage of the detonation reaction.During the middle stage of the detonation process of these aluminized explosives,the aluminum reaction reduced the attenuation of shock waves and increased the work performed by gas phase products.A higher aluminum content increased the energy output while the presence of oxidants slowed the energy release rate.This work demonstrates an effective means of evaluating the performance of aluminized explosives.

Research on the quasi-isentropic driving model of aluminized explosives in the detonation wave propagation direction

Taking CL-20(Hexanitrohexaazaisowurtzitane)-based aluminized explosives with high gurney energy as the research object, this research experimentally investigates the work capability of different aluminized explosive formulations when driving metal flyer plates in the denotation wave propagation direction.The research results showed that the formulations with 43 μm aluminum(Al) powder particles(The particle sizes of Al powder were in the range of 2~43 μm) exhibited the optimal performance in driving flyer plates along the denotation wave propagation direction. Compared to the formulations with Al powder 13 μm, the formulations with Al powder 2 μm delivered better performance in accelerating metal flyer plates in the early stage, which, however, turned to be poor in the later stage. The CL-20-based explosives containing 25% Al far under-performed those containing 15% Al. Based on the proposed quasi-isentropic hypothesis, relevant isentropy theories, and the functional relationship between detonation parameters and entropy as well as Al reaction degree, the characteristic lines of aluminized explosives in accelerating flyer plates were theoretically studied, a quasi-isentropic theoretical model for the aluminized explosive driving the flyer plate was built and the calculation methods for the variations of flyer plate velocity, Al reaction degree, and detonation product parameters with time and axial positions were developed. The theoretical model built is verified by the experimental results of the CL-20-based aluminized explosive driving flyer plate. It was found that the model built could accurately calculate the variations of flyer plate velocity and Al reaction degree over time. In addition, how physical parameters including detonation product pressure and temperature varied with time and axial positions was identified. The action time of the positive pressure after the detonation of aluminized explosives was found prolonged and the downtrend of the temperature was slowed down and even reversed to a slight rise due to the aftereffect reaction between the Al powder and the detonation products.

Study on Technology of Aluminizing and Internal Oxidation on Surface of Cu-Al-Y Alloy

Aluminum was deposited by diffusion into Cu-Al-Y alloy substrates by the pack-cementation process.Diffusion was carried out in two kinds of container with pot-type and can-type,and the results are presented.The effects of various time and temperature on the coating characteristics of Cu-Al-Y was also investigated.The result shows that the diffusion layer is nearly 170-200μm in thickness by aluminizing treatment at 900-950℃for 6-8 h in pot-type container.The aluminized layers were observed by a scanning electron micrograph(SEM),we can found:A uniform coating was achieved on Cu-Al-Y alloy surface,relatively uniform thickness and even interfaces between the layers and the substrate.The diffusion coefficient of Al in Cu-Al-Y alloys at 900℃in pot-type container can be calculated is 3.65×10-12 m 2 /s.

Cu-Zn-based alloy/oxide interfaces for enhanced electroreduction of CO_(2) to C_(2+) products

The electrochemical CO_(2)reduction reaction to produce multi-carbon(C_(2+)) hydrocarbons or oxygenate compounds is a promising route to obtain a renewable fuel of high energy density.However,producing C_(2+)at high current densities is still a challenge.Herein,we develop a Cu-Zn alloy/Cu-Zn aluminate oxide composite electrocatalytic system for enhanced conversion of CO_(2)to C_(2+)products.The Cu-Zn-Al-Layered Double Hydroxide(LDH) is used as a precursor to decompose into uniform Cu-Zn oxide/Cu-Zn aluminate pre-catalyst.Under electrochemical reduction,Cu-Zn oxide generates Cu-Zn alloy while Cu-Zn aluminate oxide remains unchanged.The alloy and oxide are closely stacked and arranged alternately,and the aluminate oxide induces the strong electron interaction of Cu,Zn and Al,creating a large number of highly active reaction interfaces composed of 0 to+3 valence metal sites.With the help of the interface effect,the optimized Cu_(9)Zn_(1)/Cu_(0.8)Zn_(0.2)Al_(2)O_(4)catalyst achieves a Faradaic efficiency of 88.5% for C_(2+)products at a current density of 400 mA cm^(-2)at-1.15 V versus reversible hydrogen electrode.The in-situ Raman and attenuate total reflectance-infrared absorption spectroscopy(ATR-IRAS) spectra show that the aluminate oxide at the interface significantly enhances the adsorption and activation of CO_(2)and the dissociation of H2O and strengthens the adsorption of CO intermediates,and the alloy promotes the C-C coupling to produce C_(2+)products.This work provides an efficient strategy to construct highly active reaction interfaces for industrial-scale electrochemical CO_(2)RR.

Research of detonation products of RDX/Al from the perspective of composition

Aluminized explosives exhibit excellent performance because the oxidation of aluminum(Al)powders enhances the pressure and temperature of detonation products.However,the equation of state(EOS)of detonation products has not been understood well.In the present study,we conducted long-time tests(approximately 1 ms)of a metal rod driven by detonation products of RDX,RDX/Li F,and RDX/Al.In addition,we used laser velocimetry(PDV)to measure the freesurface velocity of the rod.Thermochemical code DLCHEQ was successfully applied to the hydrodynamic program SSS to perform the roddriven test,and a novel method was established to study the EOS of detonation products from the perspective of composition.The reliability of DLCEHQ was validated by a small deviation(<10%)between the experimental rod free-surface velocity of RDX and the calculated results;the deviation was considerably less than that from the results obtained using the JWL EOS and ideal-gas EOS.The endothermic process and the reaction of Al powders(Al+H_(2)O+NO+CO_(2)→CO+H_(2)+N_(2)+Al_(2)O_(3))were analyzed by calculating the rod free-surface velocity of RDX/Li F and RDX/Al,respectively.The results of the present study demonstrated that the thermodynamic state of Al powders has notable influence on the EOS of aluminized detonation products,and the findings were compared with those of previous studies.First,the temperature equilibrium between Al powders and CHNO products is not always achieved,and the disequilibrium is more obvious when the reaction of Al powders is stronger.Second,the reaction rate of Al powders depends on pressure and Al content.Finally,the endothermic process of Al powders has a high contribution to the decrease in the work ability of RDX/Al instead of the gasconsumption mechanism of the Al reaction.More than half of the reaction heat of Al powders is used to heat itself,whereas the gas consumption during the reaction is negligible.

Effect of Hydrated Calcium Aluminate Cement on the Chloride Immobilization of Portland Cement Paste

To improve the efficiency and stability of chloride immobilization of portland cement paste,hydrated calcium aluminate cement(HCAC)prepared by wet grinding of CAC was added into portland cement paste as an additive.The immobilized chloride ratio(ICR)was evaluated,and the mechanism of chloride immobilization was researched by XRD,DTG,NMR,and MIP tests.The analysis results demonstrated that HCAC could improve the chloride immobilization capacity of portland cement paste.The mechanism was attributed to the following aspects:chemical binding capacity was enhanced via producing more Kuzel’s salt;physical adsorption capacity was reduced by decreasing the C-S-H gel;migration resistance was enhanced through refining the pore structure.

Chloride Corrosion of Reinforced Calcium Aluminate Cement Mortar

This paper describes a study on the corrosion behavior of steel reinforcement in CAC mortars via electrochemical methods including corrosion potential,electrochemical impedance,and linear polarization evaluation.Results indicate that there is a non-linear relationship between the corrosion degree of steel reinforcement in CAC mortar and the concentration of NaCl solution.The electrochemical parameters of specimens immersed in 3%NaCl solution suddenly drop at 40 days,earlier than 60 days of the reference.And the charge transfer resistivity of the specimen has decreased by 11 orders of magnitude at 40 days,showing an evident corrosion on steel reinforcement.However,it is interesting to notice that the corrosion is delayed by high external chloride concentration.The specimens immersed in 9%and 15%NaCl solutions remain in a relatively stable state within 120 days with slight pitting.The great corrosion protection of CAC concrete to embedded steel bars enables its wide application in marine.

Post-mortem Microstructural Study of Aluminous Refractory Brick Used in Channels of Blast Furnaces

Aluminous refractory materials with high alumina contents are widely used in the steel industry,and the higher the alumina content,the higher the working temperature.Properties such as high refractoriness and thermal shock resistance lead these refractory materials to be used as channel linings of blast furnaces,where they are exposed to the attack by slag,molten steel,working cycles and sudden temperature changes between 25℃(room temperature)and 1520℃(the temperature of molten pig iron).In this work,microstructural changes in post-mortem aluminous refractory bricks were investigated by apparent porosity,X-ray diffraction analysis(XRD),Fourier transform infrared spectroscopy(FTIR),scanning electron microscopy,and X-ray dispersion energy spectrometry(SEM/EDS).The results showed an increase in the apparent porosity and the bulk density and the presence of the phases mullite,sillimanite,alumina,and quartz in the post-mortem brick.Calcium and magnesium were not detected in the microstructure of the post-mortem brick,indicating that slags did not corrode these refractory materials.Therefore,the microstructural changes that occurred in the post-mortem bricks must be due to thermal cycling.In the X-ray diffraction(XRD)test,mullite,sillimanite,quartz,andα-alumina phases were identified.These results indicate that the aluminous refractory was obtained from sillimanite.In infrared spectroscopy(FTIR)it was possible to identify the vibration bands referring to the Si-O and Al-O bonds.The increase in the porosity is a result of cracks caused by work cycles at high temperatures and the temperature gradient to which the refractory was subjected during use.Through the micrograph it was possible to identify the presence of acicular mullite.The absence of magnesium and calcium in the microanalysis results by energy dispersed X-ray spectrometry(EDS)indicates that there was no infiltration by slag or liquid iron.These results indicate that the microstructural changes that occurred in the post-mortem aluminous refractory were of a thermal nature.

Fluoride Ion Adsorption Effect and Adsorption Mechanism of Self-Supported Adsorbent Materials Based on Desulfurization Gypsum-Aluminate Cement

The adsorption method has the advantages of low cost,high efficiency,and environmental friendliness in treating fluorinated wastewater,and the adsorbent material is the key.This study combines the inherent anion-exchange adsorption properties of layered double hydroxides(LDHs).Self-supported porous adsorbent materials loaded with AFm and AFt were prepared from a composite cementitious system consisting of calcium aluminate cement(CAC)and flue gas desulfurization gypsum(FGDG)by chemical foaming technique.The mineral composition of the adsorbent material was characterized by X-ray diffraction(XRD)and Scanning electron microscopy(SEM).Through the static adsorption experiment,the adsorption effect of the mineral composition of the adsorbent on fluoride ions was deeply analyzed,and the adsorption mechanism was revealed.XRD and SEM showed that the main hydration phases of the composite cementitious system consisting of CAC and FGDG are AFm,AFt,AH_(3),and CaSO_(4)·2H_(2)O.FGDG accelerates the hydration process of CAC and inhibits the transformation of AFt to AFm.The AFt content increased,and the AFm content decreased or even disappeared as the amount of FGDG increased.Static adsorption experiment results showed that AFm and AFt in adsorbent materials could significantly enhance the adsorption of fluoride ions.The adsorption of F^(−)in aqueous solution by PAG tends more towards monolayer adsorption with a theoretical maximum capacity of 108.70 mg/g and is similar to the measured value of 112.77 mg/g.

Effect of Al Powder and Si Powder Additions on Structure and Properties of Unburned Magnesium Aluminate Spinel Refractories

Unburned magnesium aluminate spinel refractories were prepared using sintered magnesium aluminate spinel as the main raw material,phenolic resin as the binder,aluminum powder(2%,4%,and 6%by mass)and silicon powder(when Al powder addition is 4%,Si powder addition varies:1%and 2%,by mass)as additives.The effects of the Al powder and Si powder additions on the properties and microstructure of the refractories heat treated at different temperatures(1000,1400,and 1600℃for 3 h)were studied.The results show that the Al powder addition can greatly enhance the cold modulus of rupture of the samples fired at 1000 or 1400℃,and meanwhile AlN reinforcement phase forms in the matrix,which greatly improves the hot modulus of rupture of the samples at 1400℃;however,the heat treatment at 1600℃has little influence on the strength;the addition of Al powder and Si powder results in the formation of low melting point phases,greatly reducing the hot modulus of rupture.However,the low melting point phases promote sintering,which enhances the density and the cold modulus of rupture,and decreases the volume change during heating.The samples added with Al and Si all have higher cold modulus of rupture than those added with Al powder only.

Effect of ZrO_(2)Addition on Lanthanum Aluminate-based High Emissivity Coating Materials

In order to enhance the sintering resistance of lanthanum aluminate based high emissivity coatings,Ca^(2+)-Fe^(3+)doped LaAlO_(3)/ZrO_(2)specimens were prepared by solid state sintering using La_(2)O_(3),Al_(2)O_(3),CaCO_(3) and Fe_(2)O_(3) as raw materials,extra-adding fused Y_(2)O_(3)-stabilized ZrO_(2)(0,5%,10%,and 15%,by mass),ball milling,pre-calcining,pressing into shapes and sintering at 1600℃for 2 h.The effect of the ZrO_(2)addition on the properties of lanthanum aluminate based high emissivity coatings was explored.It is concluded that ZrO_(2)does not react with LaAlO_(3),which can inhibit the sintering of the specimens.With the increase of the ZrO_(2),addition,the linear shrinkage rate and the thermal conductivity decrease significantly,while the emissivity decreases,but the emissivity of all the specimens is all higher than 0.9.The optimal addition of ZrO_(2),is 10%.

Geochemical Mobility Associated to Gold and Base Metal Occurrences of Mangodara Sector, in Southern Burkina Faso, Banfora Greenstone Belts (West African Craton)

In the Mangodara area within the Banfora greenstone belts (Baoulé-Mossi domain of the West African Craton), our study focused on geochemical assessment of the mobility of major and trace elements. Gold and base metal occurrences are hosted in highly metamorphic felsic (metarhyolite) and intermediate (metadacite and metaandesite) formations. Common mineral assemblages made up of staurolite - kyanite - pyrophyllite are interpreted to represent the metamorphosed equivalent of aluminous hydrothermal alteration. Associated felsic and intermediate volcanic rocks are enriched in Fe2O3, K2O (metaandesite, metarhyolite) and depleted in MgO, Al2O3, CaO, P2O5, Na2O (metarhyolite) and Fe2O3, MgO, CaO (metaandesite). Al2O3 depletion in mineralized kyanite-staurotide bearing metarhyolites suggests corroded minerals. Mineralized metarhyolites show enrichment in Au, Ag, Ba, Bi, Cr, Cu, Eu, La, Mo, Ni, Pb, S, Sc, V and depletion in As Sb Co, Sn, Zn while mineralized metaandesites show enrichment in Au, Ag, As, Mo, S, Sb and depletion in Co, Sn, Zn, Bi, Cr, Cu, Eu, Ni, Pb, Sc. Ba, La, V are immobile in metaandesites. Finally, Ag, As, Sn appear as geochemical vectors for gold exploration in the study area since gold mineralization is characterized by Au + Ba + Cu + Eu + La + Mo + Ni + S association in metarhyolites and Au + S + Sb + As + Ag + Bi in metaandesites.

A STUDY ON ALUMINIDE COATINGS ON TiAl ALLOYS BY PACKCEMENTATION METHOD

The halide-activated pack cementation method is utilized to deposit aluminide coat- ings on TiAl alloys. Emphasis is placed on the effect of alloying elements on the aluminizing behavior of TiAl alloy. The addition of a small amount of Nb or Cr in the TiAl improves significantly the aluminizing kinetics of TiAl alloys by increasing the solid-state division of Al through the formation of stable TiAl3 layer. The TiAl3 layer formed on the TiAl alloyed with Nb or Cr has better toughness than the TiAl3 formed on the non-alloyed TiAl. The reason for better toughness of the coating formed on TiAl is that partial TiAl3 with tetragonal structure was changed to high symmetry cubic L12 structure since Nb or Cr was dissolved into TiAl3. The TiAl3 layer formed on the TiAl alloyed with Nb or Cr has much better oxidation resistance than the TiAl3 layer formed on the non-alloyed TiAl. It is attributed to change in the crystal structure of TiAl3 from the brittle tetragonal DO22 to the ductile cubic L12 by addition of small amount of Nb or Cr.

Formation of microstructural features in hot-dip aluminized AISI 321 stainless steel

Hot-dip aluminizing（HDA） is a proven surface coating technique for improving the oxidation and corrosion resistance of ferrous substrates. Although extensive studies on the HDA of plain carbon steels have been reported, studies on the HDA of stainless steels are limited. Because of the technological importance of stainless steels in high-temperature applications, studies of their microstructural development during HDA are needed. In the present investigation, the HDA of AISI 321 stainless steel was carried out in a pure Al bath. The microstructural features of the coating were studied using scanning electron microscopy and transmission electron microscopy. These studies revealed that the coating consists of two regions： an Al top coat and an aluminide layer at the interface between the steel and Al. The Al top coat was found to consist of intermetallic phases such as Al_7Cr and Al_3Fe dispersed in an Al matrix. Twinning was observed in both the Al_7Cr and the Al_3Fe phases. Furthermore, the aluminide layer comprised a mixture of nanocrystalline Fe_2Al_5, Al_7Cr, and Al. Details of the microstructural features are presented, and their formation mechanisms are discussed.