Modification Behavior of Trace Rare Earth on Impurity Phases in Commercial Purity Aluminum

Modifying effect and mechanism of trace rare earth on Fe(Si) rich impurity phases in commercial purity aluminum were studied with the aids of SEM, EDAX, TEM, etc. It is found that Ce rich mixed rare earth (RE) is an effective modifying agent, which makes the coarse Fe rich impurity phases transform into complex compounds of tiny, sphere/short stick form, thus improving mechanical properties of this material; its modifying mechanism is in that RE gathering in front of solid/liquid interface enters into the impurity phases, forming complex (AlFeSiRE) compounds; or is adsorbed in the impurity phases surface, impeding the growth of impurity phases; however, excessive RE will result in the increasing of RE compounds (secondary phases), and plasticity reduction of this material. Therefore, its addition amount should be less than 0 07% (mass fraction).

Effects of RE,V,Ti and B composite modification on the microstructure and properties of high chromium cast iron containing 3% molybdenum

The effects of RE, V, Ti and B on the microstructure and properties of high chromium cast iron containing 3% molybdenum under as-cast and heat treatment conditions were investigated with the method of comparing experiments. The results show that with the increase of RE content, the primary austenite of high chromium cast iron is obviously refined. The morphology of carbide is changed from netlike and lath to small multiangular isolated blocks or massive blocks, the isolated degree of carbide is improved obviously, and the size is significantly refined. The addition of V and B into high chromium cast iron can refine the microstmcture, reduce coarse columnar crystals and make the carbide smaller and uniform. Through composite modification with RE, V, Ti and B, the hardness, wear resistance and impact toughness of high chromium cast iron are increased conspicuously. After heat treatment, the hardness of high chromium iron is increased significantly, but the toughness and wear resistance do not show great improvement.

Modification and refinement mechanism of Mg_2Si phase in Sr-containing AZ61-0.7Si magnesium alloy

The effect of Sr on modification and refinement of the Mg 2 Si phase in an AZ61-0.7Si magnesium alloy has been investigated and analyzed.The results indicate that Sr can effectively modify and refine the Chinese-script shaped Mg2Si phase in the AZ61-0.7Si alloy.By adding 0.06wt.%-0.12wt.%Sr to AZ61-0.7Si alloy,the Mg2Si phase in the alloy can be changed from the initial coarse Chinese-script shape to fine granule and/or irregular polygonal shapes.Accordingly,the Sr-containing AZ61-0.7Si alloy exhibits higher tensile and creep properties than the AZ61-0.7Si alloy without Sr modification.The mechanism on modification and refinement of the Mg2Si phase in Sr-containing AZ61-0.7Si alloy is possibly related to the following two aspects:(1)adding Sr may form the Al4Sr phase which can serve as the heterogeneous nucleus for the Mg2Si particles and/or(2)adding Sr may lower the onset crystallizing temperature and increase the undercooling level.

Iron-Modification of Pyroclastic Material from PCCVC Eruption (Chile): Characterization and Application to Remove Arsenic from Groundwater

Pyroclastic material from the PCCVC eruption (Chile) was modified with iron (III) solutions leading to the formation of ferrihydrite surface deposits. The aim of the chemical treatment was to prepare an adsorbent to remove arsenic from water by using low-cost mineral wastes. Physicochemical characterization of original and modified materials was carried out by XRD, BET-N2 adsorption, SEM-EDS microscopy and ICP-AES chemical analysis. The modified ash revealed that the increase of bulk iron content was close to 5% (expressed as Fe2O3) whereas surface values were 20.6% Fe2O3. Surface properties showed an increase of BET specific surface with prevalence of mesopores and an increase of total pore volume attributed to presence of nanoscopic iron phase. Kinetic and equilibrium studies were directed to optimize the operative conditions related to the material adsorptive capacity for removing arsenate species. Hence, the adsorbent dose, contact time, pH, stirring and sedimentation were evaluated in batch process. The optimal adsorption dose was 40 g ·L-1 and the solid-liquid contact time was stirring (1 h) and sedimentation (23 h), enough to ensure an adequate turbidity value valid for a pH range between 3.77 and 8.95. The analysis of the isotherm equilibrium by using the Langmuir linear method showed a R2 = 0.995 value. The performance of the treatment to remove arsenic by using a cost-effective adsorbent prepared from volcanic material is a promising technology to apply in the environmental field.

A Novel Method for Modification of SMPU by Micro-phase Separation Promoters

A novel method of controlling the shape memory properties of shape memory polyurethane （SMPU） by addition of micro-phase separation promoters including 1-octadecanol （ODO） and liquid paraffin （LP） is reported. The results indicate that the strain recovery temperature and the strain modulus rate （Eg/Er） were increased significantly with addition of small amount of micro-phase separation promoters. Thus it can increase the shape memory fixity rate and other shape memory behaviors of SMPU.

Modification of ash flow properties of coal rich in calcium and iron by coal gangue addition

Flow property of coal ash and slag is an important parameter for slag tapping of entrained flow gasifier.The viscosity of slag with high contents of calcium and iron exhibits the behavior of a crystalline slag,of which viscosity sharply increases when temperature is lowered than temperature of critical viscosity(TCV).The fluctuation in temperature near the TCVcan cause an accumulation of slag inside the gasifier.In order to prevent slag blockage,it is necessary to adjust the ash composition by additive to modify the flow property of coal rich in calcium and iron.Main components of coal gangue are Al_(2)O_(3) and SiO_(2),which is a potential additive to modify the ash flow properties of these coals.In this work,we investigated the ash flow properties of a typical coal rich in calcium and iron by adding coal gangue with different SiO_(2)/Al_(2)O_(3)ratio.The results showed that the ash fusion temperatures(AFTs)firstly decreased,and then increased with increasing amount of coal gangue addition.Chemical composition of coal ash rich in calcium and iron moved from gehlenite primary phase to anorthite,quartz and corundum primary phases.The slags with coal gangue addition behaved as a glassy slag,of which the viscosity gradually increased as temperature decreased.Besides,a high SiO_(2)/Al_(2)O_(3)ratio of coal gangue was beneficial to modify the slag viscosity behavior.Addition of coal gangue with a high SiO_(2)/Al_(2)O_(3)ratio impeded formation of crystalline phases during cooling.This work demonstrated that coal gangue addition was an effective way to improve the ash flow properties of the coal rich in calcium and iron for the entrained flow gasifier.

Comparison of Sb and Sr on modification and refinement of Mg_2Si phase in AZ61-0.7Si magnesium alloy

The effects of Sb and Sr on the modification and refinement of Mg2Si phase in an AZ61-0.7Si magnesium alloy were investigated and compared. The results indicate that the difference of Sb and Sr in the modification and refinement of Mg2Si phase is significant. Addition of 0.4%Sb(mass fraction) to AZ61-0.7Si alloy can refine but not modify Mg2Si phase. Oppositely,by addition of 0.12%Sr to AZ61-0.7Si alloy,the Mg2Si phase changes from initial coarse Chinese script shape to fine granule and/or irregular polygonal shape. Accordingly,the Sr-modified AZ61-0.7Si alloy exhibits higher tensile and creep properties than the Sb-modified one. The difference of Sb and Sr in the modification and refinement of Mg2Si phase is possibly related to the following two aspects:1) the disregistry at(100)Al4Sr//(100)Mg2Si is lower than that at(0001)Mg3Sb2//(111)Mg2Si(0.69% vs 1.72%) and 2) the onset crystallizing temperature of the Sr-modified AZ61-0.7Si alloy is lower than that of the Sb-modified one(603.1 ℃ vs 606.9 ℃).

Thermodynamic data calculation for iron phases in sulfoaluminate cementitious materials prepared using solid wastes

The preparation of sulfoaluminate cementitious materials(SCM)is a promising way to massively utilize solid wastes.Iron phases are significant in SCM system but the thermodynamic data of some key minerals,such as6 CaO·Al2 O3·2 Fe2 O3(C6 AF2)and 6 CaO·2 Al2 O3·Fe2 O3(C6 A2 F),are missing,which greatly hinders the SCM optimization in a theoretical way.This work,for the first time,calculated the standard formation enthalpy,Gibbs free energy of formation,entropy and molar heat capacity for C6 AF2 and C6 A2 F and lowered the errors to the least with the reference of C4 AF data in the literature.By building the function diagram of Gibbs free energy changes with temperature for the basic iron phase formation reactions with the obtained thermodynamic data,it is proved that the formation likeliness of C6 AF2 is higher than that of C6 A2 F,as is accordant to the literatures and verifies the correctness of obtained data.This work provides a good theoretical foundation to optimize SCM mineral system and to study relevant mechanism deeply.

Distribution and Influence of Iron Phases on the Physico-Chemical Properties of Phyllosilicates

Clay minerals from different Cretaceous stratigraphic successions of Egypt were investigated using XRD, DTA, dissolution analysis (DCB), IR, M*issbauer and X-band Electron Spin Resonance (ESR) spectroscopies. The purity of the samples and the degree of structural order were determined by XRD. The location of Fe in the octahedral sheet is characterized by absorption bands at ～875 cm\+\{-1\} assigned as Al-OH-Fe which is present after chemical dissolution of free iron. The M*issbauer spectra of these clays show two doublets with isomer shift and quadrupole splitting typical of octahedral coordinated Fe\+\{3+\}, in addition to third doubler with hyperfine parameter typical of Fe\+\{2+\} in the spectra of Abu-Had kaolinite (H) sample. 6-lines magnetic hyperfine components which are consistent with those of hematite are confirmed in the spectra of both Isel and Rish kaolinite samples. Goethite was confirmed by both IR and DTA. Multiple nature of ESR of these clays suggested structural Fe in distorted octahedral symmetry and as non-structural Fe. Little dispersion and low swelling indices as well as incomplete activation of investigated montmorillonite samples by NaCO\-3 appear to be due to incomplete disaggregation of montmorillonite particles. This can be explained by the ability of Fe-gel to aggregate the montmorillonite into pseudo-particles and retard the rigid-gel structure. However, extraction of this ferric amorphous compound by dithonite treatment recovers the surface properties of the montmorillonite samples. On the other hand, amounts and site occupation of Fe associated with kaolinite samples show a negative correlation with the parameters used to describe the degree of crystalline perfection, color, brightness and vitrification range of these kaolinite samples.

Distribution and Influence of Iron Phases on the Physico-Chemical Properties of Phyllosilicates

Clay minerals from different Cretaceous stratigraphic successions of Egypt were investigated using XRD, DTA, dissolution analysis (DCB), IR, Mssbauer and X\|ray Electron Spin Resonance (ESR) spectroscopes. The purity of the samples and the degree of their structural order were determined by XRD. The location of Fe in the octahedral sheet is characterized by absorption bands at ～875cm\+\{-1\} assigned as Al\|OH\|Fe which persist after chemical dissolution of free iron. The Mssbauer spectra of these clays show two doublets with isomer shift and quadrupole splitting typical of octahedrally coordinated Fe\+\{3+\}, in addition to third doublet with hyperfine parameter typical of Fe\+\{2+\} in the spectra of Abu\|Had kaolinite (H) sample. Six\|lines magnetic hyperfine components which are consistent with those of hematite are confirmed in the spectra of both Isel and Rish kaolinite samples. Goethite was confirmed by both IR and DTA. Multiple nature of ESR of these clays suggested structural Fe in distorted octahedral symmetry as well as non\|structural Fe.\; Little dispersion and low swelling indices as well as incomplete activation of the investigated montmorillonite samples by NaCO\-3 appear to be due to incomplete disaggregation of montmorillonite particles. This can be explained by the ability of Fe\|gel to aggregate the montmorillonite into pseudo\|particles and retard the rigid\|gel structure. However, extraction of this ferric amorphous compound by dithonite treatment recovers the surface properties of the montmorillonite samples.\; On the other hand, the amount and site occupation of Fe associated with kaolinite samples show an inverse correlation with the parameters used to describe the degree of crystallinity perfection, color, brightness and vitrification range of these kaolinite samples.

Distributions of Sr and Fe and their influence on modification of hypoeutectic Al-Si alloy

The influence of cooling rate and Fe-containing phases on Sr-modification of Si phases in hypoeutectic Al-Si alloys, a problem with great industrial importance, was investigated. The microstructures of samples were examined using scanning electron microscopy(SEM) with energy-dispersive X-ray spectroscopy(EDX). A new method of electron probe microanalysis(EPMA) map scanning was used to analyze the Sr distribution, which gave quantitative results covering more Si particles. EPMA map scanning, together with SEM with EDX, was also used in analyzing the distribution of Fe phases. Results show that Fe-containing phase was related to the unmodified Si particles in samples with partial modification failure and the plate-like Si phases in samples without modification failure. Such a relationship was further confirmed by the microstructure observation.In conclusion, a partial failure of Sr-modification can be caused by both slow cooling rate and Fe-containing phases.

Direct observation of shock-induced phase transformation in polycrystalline iron via in situ x-ray diffraction

Phase transition of polycrystalline iron compressed along the Hugoniot is studied by combining laser-driven shock with in situ x-ray diffraction technique.It is suggested that polycrystalline iron changes from an initial body-centered cubic structure to a hexagonal close-packed structure with increasing pressure(i.e.,a phase transition fromαtoε).The relationship between density and pressure for polycrystalline iron obtained from the present experiments is found to be in good agreement with the gas-gun Hugoniot data.Our results show that experiments with samples at lower temperatures under static loading,such as in a diamond anvil cell,lead to higher densities measured than those found under dynamic loading.This means that extrapolating results of static experiments may not predict the dynamic responses of materials accurately.In addition,neither the face-centered cubic structure seen in previous molecular-dynamics simulations or twophase coexistence are found within our experimental pressure range.

Preparation and modification of VO_2 thin film on R-sapphire substrate by rapid thermal process

The VO2 thin film with high performance of metal-insulator transition （MIT） is prepared on R-sapphire substrate for the first time by magnetron sputtering with rapid thermal process （RTP）. The electrical characteristic and THz transmittance of MIT in VO2 film are studied by four-point probe method and THz time domain spectrum （THz-TDS）. X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, atomic force microscopy （AFM）, and search engine marketing （SEM） are employed to analyze the crystalline structure, valence state, surface morphology of the film. Results indicate that the properties of VO2 film which is oxidized from the metal vanadium film in oxygen atmosphere are improved with a follow- up RTP modification in nitrogen atmosphere. The crystallization and components of VO2 film are improved and the film becomes compact and uniform. A better phase transition performance is shown that the resistance changes nearly 3 orders of magnitude with a 2-~C hysteresis width and the THz transmittances are reduced by 64% and 60% in thermal and optical excitation respectively.

Preparation and modification of nano-sized Al_2O_3 powders through addition of oxide

Ammonium aluminum carbonate hydroxide（AACH）, the precursor of α-Al2O3, was fabricated with NH4Al（SO4）2 and NH4HCO3 via a precipitation method. During the heat treatment AACH undergoes such a phase transformation process: amorphous（350℃）→γ（700℃）→γ+θ（1050℃）→θ+α （1100℃）→α （1200℃）. Oxides, such as TiO2 sol and MgO sol were introduced into the precursor. Then both the α transformation temperature and the particle sizes of α-Al2O3 are decreased. The microstructures and its surface electronic properties of the powders are modified, and its dispersion property is improved. Doping TiO2 sol grains, AACH completes α phase transformation nearly at 1100℃, its first-order diameter is about 120nm. Doping with MgO sol grains, α phase transformation completes after being sintered at 1100℃.

Investigation of the Boriding Process of the Ti-Al Intermetallic Alloy GE48-2-2 Taking into Account the Probability of the Influence of the Substrate Modification

Boriding of the Ti-Al intermetallic GE48-2-2 at 1273 K for 10 hours was performed. In order to ensure that no any serious alteration occurred in the substrate, it was previously examined with X-Ray Diffractometry (XRD), after it has undergone an annealing process at the temperature of boronizing. Subsequently, we examined the coating with XRD and Scanning Electron Microscopy, in order to characterize its structure and morphology. A dense TiΒ2 layer, 10 - 15 μm thick, was formed, but also Cr2B3 and NbN, BN and some Ti-Al phases were detected. Efforts were undertaken to focus on influence of the substrate modification, towards the quality of the coating.

Mini Review: Chemical Mesoscopics Notions in the Explanation of Polymeric Materials Modification Mechanism with Participation of Metal Carbon Mesocomposites

The paper is dedicated to the consideration of the chemical mesoscopics notions application for the explanation of polymeric materials modification mechanism by the metal carbon mesoscopic composites.The main peculiarities of these nanosized particles are following:a)the presence of unpaired electrons on the carbon cover;b)the structure of carbon cover consists from poly acetylene and carbine fragments;c)the atomic magnetic moment of inner metal is equaled to more than 1,3μB.The metal carbon mesocomposites activity depends on the medium and conditions influence because of the possible changes of the phase coherency and quantization of negative charges.

Synthesis and modification of spherical/hollow metal-organic frameworks for efficient extraction of sulfonamides in aqueous environments

In this study,two novel spherical/hollow metal-organic frameworks were successfully synthesized,and further modified by a mild non-covalent modification strategy with dopamine and 1,4-benzenedithiol(BDT)as polymeric monomers to obtain pB DT@PDA-Ni-MOF and p BDT@PDA-Ni/Co-MOF,respectively.The results showed that the above MOFs possessed extremely fast adsorption rates and ideal adsorption capacities for sulfonamides(SAs)and the modified MOFs exhibited enhanced adsorption capacities for SAs owing to a large number of additional functional groups.Then,benefit of their regular morphology and size,a facile syringe-assisted dispersive solid phase extraction(S-DSPE)method was developed for efficient detection of SAs,which will provide a powerful tool for monitoring trace level of SAs in aqueous environment.

Revealing the atomic mechanism of diamond–iron interfacial reaction

Diamond,with ultrahigh hardness,high wear resistance,high thermal conductivity,and so forth,has attracted worldwide attention.However,researchers found emergent reactions at the interfaces between diamond and ferrous materials,which significantly affects the performance of diamond-based devices.Herein,combing experiments and theoretical calculations,taking diamond–iron(Fe)interface as a prototype,the counter-diffusion mechanism of Fe/carbon atoms has been established.Surprisingly,it is identified that Fe and diamond first form a coherent interface,and then Fe atoms diffuse into diamond and prefer the carbon vacancies sites.Meanwhile,the relaxed carbon atoms diffuse into the Fe lattice,forming Fe_(3)C.Moreover,graphite is observed at the Fe_(3)C surface when Fe_(3)C is over-saturated by carbon atoms.The present findings are expected to offer new insights into the atomic mechanism for diamondferrous material's interfacial reactions,benefiting diamond-based device applications.

Solubility of iron(Ⅲ) and nickel(Ⅱ) acetylacetonates in supercritical carbon dioxide

As a common precursor for supercritical CO_(2)(scCO_(2))deposition techniques,solubility data of organometallic complexes in scCO_(2)is crucial for the preparation of nanocomposites.Recently,metal acetylacetonates have shown great potential for the preparation of single-atom catalytic materials.In this study,the solubilities of iron(Ⅲ)acetylacetonate(Fe(acac)3)and nickel(Ⅱ)acetylacetonate(Ni(acac)2)were measured at the temperature from 313.15 to 333.15 K and in the pressure range of 9.5–25.2 MPa to accumulate new solubility data.Solubility was measured using a static weight loss method.The semi-empirical models proposed by Chrastil and Sung et al.were used to correlate the solubility data of Fe(acac)3 and Ni(acac)2.The equations obtained can be used to predict the solubility of the same system in the experimental range.