Finite Element Analysis of Large Size Chromium Oxide Green Bodies During Firing

To prevent dense chromium oxide covers from cracking during firing,such as internal cracking,surface cracking and fracture,the firing process of dense chromium oxide products was simulated,and the performance parameters at several specific temperatures before and after densification of chromium oxide green bodies were tested.The temperature difference and the stress difference of chromium oxide green bodies were calculated by Finite Element Software at heating and cooling rates of 10,20,30 and 40℃·h^(-1),respectively.The results show that large temperature difference and thermal stress difference are the main causes of internal cracking,surface cracking and fracture of the brick.Suitable heating rates reduce or avoid internal cracking of the brick.When the heating rate is 30℃·h^(-1) below 1450℃and 10℃·h^(-1) above 1450℃,the temperature difference and the thermal stress difference in the brick are below 4℃and 4 MPa,respectively,and there is no internal crack in the brick after firing.The initial cooling stage is the key stage that causes cracking or fracture of bricks.When the cooling rate is 20℃·h^(-1) above 1450℃,the thermal stress difference in the brick is less than 4 MPa,which can significantly reduce the surface cracks and fracture of the brick.

Reduction of chromium oxides in stainless steel dust

The recovery of metal oxides from stainless steel dust using C（graphite）, SiFe, and Al as reductants was investigated under various conditions. The apparent distribution ratio of Cr（L Cr ′^m/s ） in the recovered metal and residual slag phases was defined as the major performance metric. The results show that the recovery ratio of metals increases as the ratio of CaO ：SiO2 by mass in the residual slag increases to 1.17. The residual content of metals in the slag decreases as the Al2O3 content of the slag is increased from approximately 8wt% to 10wt%. The recovery ratio of Cr increases with increasing L Cr ′^ m/s , and a linear relationship between L Cr ′^m/s and the activity coefficient ratio of CrO in the slag and the recovered metal phase is observed. The combination of C and SiFe or Al as the reducing agents reveals that Si is the more effective coreductant.

Preparation and Characterization of Plasma-Sprayed Ultrafine Chromium Oxide Coatings

Ultrafine chromium oxide coatings were prepared by plasma spraying with ultrafine feedstock. Processing parameters of plasma spraying were optimized. Optical microscope （OM） was used to observe the microstructure of the ultrafine chromium oxide coatings. Scanning electron microscopy （SEM） was used to observe the morphology and particle size of ultrafine powder feedstock as well as to examine the microstructure of the chromium oxide coating. In addition, hardness and bonding strength of the ultrafine chromium oxide coatings were measured. The results showed that the optimized plasma spraying parameters were suitable for ultrafine chromium oxide coating and the properties and microstructure of the optimized ultrafine chromium oxide coating were superior compared to conventional chromium oxide wear resistant coatings.

Effect of Atmosphere on Sintering Behavior of Chromium Oxide Materials

The chromium oxide materials were prepared using Cr2O3 micropowder as main starting material, TiO2 micropowder as sintering aid, polyvinyl alcohol as binder, by a series of processes such as slurrying, spraying granulation, machine moulding and cold isostatic pressing, and firing at 1 500 ℃ for 3 h in air （ oxygen partial pressure was 2. 1× 10^4 Pa ）, industrial nitrogen （ oxygen partial pressure was 1×10^3 Pa ） , pure nitrogen （ oxygen partial pressure was 10 Pa） , high purity nitrogen （ oxygen partial pressure was 0.1 Pa ） , and carbon cake embedded atmosphere （ oxygen partial pressure wtas 2.3×10-12 Pa ）. Effects of oxygen partial pressures on the sintering behavior of Cr2 O3 materials were investiga- ted. The results show that （ 1 ） for 3 wt% TiO2-doped specimeas, there is a substantial dependence of sintering on oxygen partial pressure （0. 1 Pa - 2. 1 ×10^4 Pa ） , and the bulk density increases and apparent porosity decreases with oxygen partial pressure decreasing; （2） even if the oxygen partial pressure is 0. 1 Pa, the specimen without TiO2 cannot reach densification sintering; （3） under very low oxygen partial pressure of carbon embedded atmosphere, Cr2O3 materials containing TiO2 or not can attain denzification.

Efect of chromium oxide as active site over TiO_2-PILC for selective catalytic oxidation of NO

This study introduced TiO2-pillared clays （TiO2-PILC） as a support for the catalytic oxidation of NO and analyzed the performance of chromium oxides as the active site of the oxidation process. Cr-based catalysts were prepared by a wet impregnation method. It was found that the 10 wt.% chromium doping on the support achieved the best catalytic activity. At 350℃, the NO conversion was 61% under conditions of GHSV = 23600 hr^-l. The BET data showed that the support particles had a mesoporous structure. Hz-TPR showed that Cr（10）TiP （10 wt.% Cr doping on TiO2-PILC） clearly exhibited a smooth single peak. EPR and XPS were used to elucidate the oxidation process. During the NO ＋ O2 adsorption, the intensity of evolution of superoxide ions （O2^-） increased. The content of Cr^3＋ on the surface of the used catalyst was 40.37%, but when the used catalyst continued adsorbing NO, the Cr^3＋ increased to 50.28%. Additionally, Oα/Oβ increased markedly through the oxidation process. The NO conversion decreased when SO2 was added into the system, but when the SO2 was removed, the catalytic activity recovered almost up to the initial level. FT-IR spectra did not show a distinct characteristic peak of SO4^2-.

Preparation of Chromium Oxide Coatings on Aluminum Borate Whiskers by a Hydrothermal Deposition Process

Aluminum borate whiskers (9Al 2O 3·2B 2O 3) can be used to reinforce aluminum alloys to produce light and strong composites. However, the adverse interfacial reactions between the whiskers and the aluminum alloys inhibit their practical uses; therefore, a protective coating is needed on whiskers. In this work, aluminum borate whiskers were coated with chromium coating deposits in a hydrothermal solution containing CrCl 3, Na 2C 4H 4O 6, NaPH 2O 2, and H 3BO 3. The presence of the impurity P in the hydrothermal deposits can be avoided by reducing the amount of NaPH 2O 2 in the coating solution. Thermodynamic analysis was used to discuss the behavior of ions in the coating process. The subsequent heating of the hydrothermal products in air at 800 ℃ yielded smooth Cr 2O 3 films with a thickness of 0.060.07 μm.

Influence of Target-Substrate Distance and Sputtering Power on Chromium Oxide Films Prepared by Medium-Frequency Magnetron Sputtering

Chromium oxide films were deposited on Si（100） substrates by medium-frequency（MF） unbalanced magnetron sputtering at different target-substrate distances DTS（60,100,120 mm） and sputtering power（2.8,5.6,11.2 kW）,respectively.The structure,surface morphologies,and microhardness of the chromium oxide films were examined by X-ray diffraction（XRD）,atomic force microscopy（AFM）,and microhardness tester.The results indicate that elevated MF sputtering power can improve the crystallization of the films;The DTS value affects the structure of the films by changing the preferential orientation from CrO3（221） to Cr2O3（116）;The microhardness of the chromium oxide films is found to increase with the sputtering power.For preparing the Cr2O3-dominated films with comparatively high-performance,the optimized condition is the target-substrate distance of 100 mm and MF sputtering power of 11.2 kW.

Effects of lanthanum ion-implantation on microstructure of oxide film formed on Co-Cr alloy

Isothermal and cyclic oxidizing behavior of Co-40Cr alloy and its lanthanum ion-implanted samples were studied at 1000 ℃ in the air by thermal-gravimetric analysis （TGA）. Scanning electronic microscopy （SEM） and transmission electronic microscopy （TEM） were used to examine the morphology and structure of oxide film after oxidation. Secondary ion mass spectrum （SIMS） method was used to examine the binding energy change of chromium caused by La-doping and its influence on the formation of Cr2O3 film. laser Raman spectrum was used to examine the stress changes within the oxide film. It was found that lanthanum implantation remarkably reduced isothermal oxidizing rate of Co-40Cr and improved anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvement were mainly that the implanted lanthanum reduced the grain size and internal stress of Cr2O3 oxide and increased high temperature plasticity of the oxide film. Lanthanum mainly existed on the outer surface of Cr2O3 oxide film in the form of fine La2O3 and LaCrO3 spinel particles.

Roles of Ceria on Base Metal Oxide Catalysts——NO+CO Reaction

A microreactor system was used to study the catalytic reaction of NO+CO→1/2 N_2+CO_2 over Cu,Fe, Mn,Cr,and Ce oxides supported on alumina,and the effect of adding Ce in supported Cu-M-O(M=Mn,Fe and Cr) catalysts on their catalytic activities for the topic reaction and the concentration of N_2O produced.It was found that the catalytic activity order of the single-element oxide is:CuO>Fe_2O_3≈Cr_2O_3> MnO_2>CeO_2>NiO.Cu-Mn-O is more active than CuO,and Cu-Fe-O is more active than Cu-Mn-O and Cu-Cr-O for NO+CO reaction.This study shows that the addition of Ce in supported Cu-M-O can promote their catalytic activities Jot the topic reaction,which makes the reaction of 2NO+CO→N_2O+CO_2 fast,and N_2O is an intermediate compound produced during NO+CO reaction.

Preparation and Properties of Ultra-fine Chromium Carbonization of High Performance Mechanical Activation

The preparation of hydroxyl chromium oxide by hydrogen reduction of disodium chromate and particulate hydroxyl mechanical activation features were studied. Then with self-made hydroxyl chromium as the raw material, a direct reduction and carburization process was used to prepare ultra-fine chromium carbonization. Through SEM and XRD, the high performance mechanical activation, key coefficients, microstructure, hardness and wear-resisting property were investigated. The results reveal that suitable mechanical activation and carbon reducing carbonization temperature, carbonization time, carbon content are beneficial to obtaining ultra-fine chromium carbonization. Typically, when the time of high performance grinding is 5 min, the carbon reducing temperature is 1100 ℃, the carbon reducing time is 1h, the carbon content is 28%, and finally the particle size of chromium carbide powder is 1 μm. Under this condition of preparation of ultra-fine chromium carbide, both the hardness and wear resistance are better than those in the industrialization of chromium carbide coating.

CrOx supported on high-silica HZSM-5 for propane dehydrogenation

Industrial propane dehydrogenation(PDH)catalysts generally suffer from low catalytic stability due to the coke formation onto the catalyst surface to cover the active sites.The exploitation of an efficient catalyst with both high catalytic selectivity and long-term stability toward PDH is of great importance but challenging to make.Herein CrOx supported on high-silica HZSM-5 with a SiO2/Al2O3 ratio of 260(Cr/Z-5(260)is synthesized by a simple wet impregnation method,which exhibits high catalytic activity,good selectivity and excellent stability for PDH.At a weight hourly space velocity(WHSV)of 0.59 h-1,a propylene formation rate of 4.1 mmol g-1cath-1(~32.6% propane conversion and ~94.2% propylene selectivity)can be maintained over the 5%Cr/Z-5(260)catalyst after 50 h time on stream,which is much better than commercial Cr/Al2O3(Catofin process,catalyst life is several hours)at the same reaction conditions.With increasing the WHSV to 5.9 h-1,a high propylene formation rate of 27.9 mmol gcat-1h-1can be obtained over the 5%Cr/Z-5(260)catalyst after 50 h time on stream,demonstrating a very promising PDH catalyst.Characterization results and Na+doping experiments reveal that the Cr species combined with Br?nsted acid sites in Cr/HZSM-5 catalysts are responsible for the high catalytic performance.In particular,the Br?nsted acid sites in HZSM-5 zeolite could increase the propane adsorption and enhance the C–H bond activation.Furthermore,the high surface area and well-defined pores of HZSM-5 zeolite can provide a special environment for the dispersion and stabilization of Cr species,thus guaranteeing high catalytic activity and stability.

Preparation of Cr_2O_3 precursors by hydrothermal reduction in the abundant Na_2CO_3 and Na_2CrO_4 solution

Precursors of chromium oxide （p-Cr203） were prepared by reducing hexavalent chromium in the presence of sodium carbonate solution under hydrothermal conditions. Methanal was used as the reductant, and carbon dioxide was the acidulating agent. The influences of reaction temperature, initial pressure of carbon dioxide, isothermal time and methanal coefficient on Cr（VI） reduction were investigated. Ex- perimental results showed that Cr（VI） was reduced to Cr（III） with a yield of 99%. Chemical titration, thermogravimetry （TG）, X-ray diffrac- tion （XRD） analysis, and scanning electron microscopy （SEM） were used to characterize the p-Cr203 and Cr203. The series of p-Cr203 were found to be multiphase even if they presented different colors, from gray green to lavender. After these p-Cr203 samples were calcined, the product of rhombohedral Cr203 with a purity of 99.5wt% was obtained.

Oxidative Dehydrogenation of Ethylbenzene over ZSM-5 Type Chromosilicates in the Presence of CO2

In this work, ZSM-5 type chromosilicate samples as K[Cr]ZSM-5(KCS) and Na[Cr]ZSM-5(NCS) were prepared by hydrothermal method and their catalytic properties were investigated for the oxidative dehydrogenation of ethylbenzene in the presence of CO2 as an oxidant using a fixed-bed stainless steel reactor. The prepared samples were characterized by their morphology (SEM), structural parameters (XRD), and textural parameters (BET). The performance of these catalysts was evaluated in terms of conversion, styrene yield, and selectivity. The KCSBW catalyst (potassium chromosilicate before washing with distilled water) afforded the highest styrene yield, 56.19%, with the selectivity of 96.05% in the presence of CO2 because of the coexistence of potassium ion and Cr2O3 in its structure and their synergistic effect. The influence of the presence of Cr2O3 and sodium or potassium ion on the catalytic activity of the chromosilicate samples in the catalytic EB dehydrogenation process was discussed in detail. Moreover, according to the results, the catalytic activity of the chromosilicate samples (CS) in EB dehydrogenation was increased by decreasing the surface area.

Surface Mapping of Resistive Switching CrOx Thin Films

In this work, we investigated resistive switching behavior of CrOx thin films grown by using sputtering technique. Conventional I-V measurements obtained from Ag/CrOx/Pt/Ti/SiO2/Si structures depict the bipolar switching behavior, which is controlled by formation/dissolution processes of Ag conducting filaments through electrochemical redox reaction under external electric field driven. Conductive atomic force microscopy (C-AFM) technique provides the valuable mapping images of existing Ag filaments at low resistance state as well as the characteristics of filament distributions and diameters. This study also reveals that where the higher amplitude of topography is, the easier possibility of forming conducting filament paths is on CrOx surface films.

Nano-sized Fe_2O_3/Fe_3O_4 facilitate anaerobic transformation of hexavalent chromium in soil–water systems

The purpose of this study is to investigate the effects of nano-sized or submicro Fe_2O_3/Fe_3O_4 on the bioreduction of hexavalent chromium（Cr（VI）） and to evaluate the effects of nano-sized Fe_2O_3/Fe_3O_4 on the microbial communities from the anaerobic flooding soil.The results indicated that the net decreases upon Cr（VI） concentration from biotic soil samples amended with nano-sized Fe_2O_3（317.1 ± 2.1 mg/L） and Fe_3O_4（324.0 ± 22.2 mg/L） within21 days,which were approximately 2-fold of Cr（VI） concentration released from blank control assays（117.1 ± 5.6 mg/L）.Furthermore,the results of denaturing gradient gel electrophoresis（DGGE） and high-throughput sequencing indicated a greater variety of microbes within the microbial community in amendments with nano-sized Fe_2O_3/Fe_3O_4 than the control assays.Especially,Proteobacteria occupied a predominant status on the phylum level within the indigenous microbial communities from chromium-contaminated soils.Besides,some partial decrease of soluble Cr（VI） in abiotic nano-sized Fe_2O_3/Fe_3O_4 amendments was responsible for the adsorption of nano-sized Fe_2O_3/Fe_3O_4 to soluble Cr（VI）.Hence,the presence of nano-sized Fe_2O_3/Fe_3O_4 could largely facilitate the mobilization and biotransformation of Cr（VI） from flooding soils by adsorption and bio-mediated processes.

Effect of TiO2 on reduction behavior of Cr2O3 in CaO-SiO2-Al2O3-MgO-TiO2-Cr2O3 by carbon from Fe-C melt

The chromium-bearing titanomagnetite ore will turn to be the important raw material for blast furnace process in Panxi area,China.The reduction behavior of Cr2O3 between CaO-SiO2-Al2O3-TiO2-Cr2O3 and Fe-C systems was investigated.The effect of TiO2 content in the slag system on the reduction of Cr2O3,TiO2,and SiO2 and the con sumption of C in hot metal was investigated by both theoretical calculation and physical experiment.The theoretical calculation results reveal that higher reduction temperature promotes the reduction of Cr and Ti,while high basicity and TiO2 content have little influence on the reduction of chromium but significantly influence the reduction of Ti.The smelting reduction experiment results show that the content of Cr in hot metal significantly in creases with extendi ng the reduction time and decreases with the increase in TiO2 content.However,the content of Ti in hot metal significantly increases as the TiO2 increases,reaching 0.073,0.085,0.107,and 0.121 wt.%for 5,10,15,and 20 wt.%of TiO2 input,respectively.Kinetic studies proved that the reduction of Cr2O3 was a first-order reaction.The addition of TiO2 inhibited the reduction of Cr2O3 and resulted in the decrease in reaction rate constant.