The effect of thermal cycle on joint of Ti/stainless steel phase transformation diffusion bonding

The effects of thermal cycle parameters on the tensile strength and fracture characteristics of phase transformation diffusion bonding(PTDB) joint of titanium and stainless steel (Ti/SS) were studied in this paper. With the maximum cyclic temperature of 1 173～1 223 K , the minimum cyclic temperature of 1 073～1 093 K , the heating velocity of 30～50 K/s , the cooling velocity of 15～20 K/s , the cycle numbers of 15～20 and bonding pressure is 13 MPa , the tensile strength of joint is more than 380 MPa , exceeding 80% of that of Ti.

Progress in research on diffusional phase transformations of Fe–C alloys under high magnetic fields

The solid-phase transformations of metal materials under high magnetic fields are an important topic in research on the electromagnetic processing of materials.Progress in research on the diffusional phase transformations of Fe–C alloys under high magnetic fields is reviewed.The effects of high magnetic fields on the microstructural evolution in diffusional phase transformations in Fe–C alloys are discussed.The kinetics of ferrite transformations,pearlite transformations,and the precipitation of carbides under high magnetic fields are reviewed in terms of the thermodynamics of phase transformations and the diffusion behavior of carbon atoms.Finally,future trends in research on diffusional phase transformations of Fe–C alloys under high magnetic fields are discussed.

Highly efficient photo-thermal synergistic catalysis of CO_(2)methanation over La1-xCexNiO_(3)perovskite-catalyst

Solar-driven photo-thermal catalytic CO_(2)methanation reaction is a promising technology to alleviate the problems posed by greenhouse gases emissions.However,designing advanced photo-thermal catalysts remains a research challenge for CO_(2)methanation reaction.In this work,a series of ABO3(A=lanthanide,B=transition metal)perovskite catalysts with Ce-substituted LaNiO3(La1-xCexNiO3,x=0,0.2,0.5,0.8,1)were synthesized for CO_(2)methanation.The La0.2Ce0.8NiO3 exhibited the highest CH4 formation rate of 258.9 mmol·g^(-1)·hcat-1,CO_(2)conversion of 55.4%and 97.2%CH4 selectivity at 300℃with the light intensity of 2.9 W·cm^(-2).Then the catalysts were thoroughly analyzed by physicochemical structure and optical properties characterizations.The partial substitution of the A-site provided more active sites for the adsorption and activation of CO_(2)/H_(2).The sources of the active sites were considered to be the oxygen vacancies(Ov)created by lattice distortions due to different species of ions(La^(3+),Ce^(4+),Ce^(3+))and exsolved Ni0 by H_(2)reduction.The catalysts have excellent light absorption absorbance and low electron-hole(e-/h+)recombination rate,which greatly contribute to the excellent performance in photo-thermal synergistic catalysis(PTC)CO_(2)methanation.The results of in situ irradiated electron paramagnetic resonance spectrometer(ISI-EPR)and ISI-X-ray photoelectron spectroscopy(XPS)indicated that the aggregation of unpaired electrons near the defects and Ni metal(from La and Ce ions to Ov and Ni0)accelerated adsorption and activation of CO_(2)/H_(2).At last,the catalyst properties and structure were correlated with the proposed reaction mechanism from the in situ diffuse reflection infrared Fourier transform spectrum(DRIFTS)measurements.The in situ precipitation of the B-site enhanced the dispersion of Ni,while its enriched photoelectrons upon illumination further promote hydrogen dissociation.More H^(*)spillover accelerated the rate-determining step(RDS)of HCOO*hydrogenation.This work provides the theoretical basis for the development of catalysts and industrial application.

Transformation of Anaplastic Large Cell Lymphoma to High-grade Diffuse Large B-cell Ymphoma:Remission after Pegylated Liposomal Doxorubicin and Rituximab Immunotherapy

Summary:We demonstrate the usefulness of pegylated liposomal doxorubicin (PL-doxorubicin) combine with CD20 antibody Rituximab in a case of transformation of anaplastic large cell lymphoma (ALCL) to high-grade diffuse large B-cell lymphoma (B-DLCL).Case report:A 63-year-old woman suffering from anaplastic large cell lymphoma(stage Ⅳ a) since 2004 showed mediastinal relapse despite of 4 cyclesof chemotherapy following the

Effect of Deep Cryogenic Treatment on Formation of Reversed Austenite in Super Martensitic Stainless Steel

The effect of deep cryogenic treatment on the formation of reversed austenite （RA） in super martensitic stainless steel was investigated. RA was found to form in steels without （A） and with （B） deep cryogenic treatment. The volume fraction of RA initially increased and then decreased with increasing tempering temperature over 550-- 750 ℃ for the two steels, which were quenched at 1050 ℃. In addition, for both with and without deep cryogenic treatment, the RA content reached a maximum value at 650 ℃ although the RA content in steel B was greater than that in steel A over the entire range of tempering temperatures. Furthermore, the hardness （HRC） of steel B was greater than that of steel A at tempering temperatures of 550--750 ℃. From these results, the basic mechanism for the formation of RA in steels A and B was determined to be Ni diffusion. However, there were more Ni enriched points, a lower degree of enrichment, and a shorter diffusion path in steel B. It needed to be noted that the shapes of the RA consisted of blocks and stripes in both steels. These shapes resulted because the RA redissolved and trans- formed to martensite along the martensitic lath boundaries when the tempering temperature was 650--750 ℃, and a portion of RA in the martensitie lath divided the originally wider martensitic laths into a number of thinner ones. In- terestingly, the RA redissolved more rapidly in steel B and consequently resulted in a stronger refining effect.

Large anisotropic negative thermal expansion in Cu-TDPAT metalorganic framework:A combined in situ X-ray diffraction and DRIFTS study

Cu-TDPAT(H_(6)TDPAT=2,4,6-tris(3,5-dicarboxylphenylamino)-1,3,5-triazine),a stable nanoporous metal-organic framework with rht topology,has sparked broad interest as an adsorbent for several chemical separation processes.In this work,in situ synchrotron diffraction experiments followed by sequential LeBail refinements reveal that Cu-TDPAT shows unusually large anisotropic negative thermal expansion(NTE).The PASCal crystallography tool,used to analyze the magnitude of the NTE,reveals an average volumetric thermal expansion coefficientαv=-20.3 MK^(-1).This value is significantly higher than the one reported for Cu-BTC(also known as HKUST-1),which contains the same Cu-paddlewheel building unit,αv=-12 MK^(-1).In situ synchrotron single crystal X-ray diffraction and in situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)were employed to shed light on the NTE mechanism.Using these two methods,we were able to elucidate the three main structural motions that are responsible for the NTE effect.The more pronounced NTE behavior of Cu-TDPAT is attributed to the lower symmetry combined with the more complex ligand structure when compared to Cu-BTC.The knowledge obtained in this work is important for understanding the behavior of the adsorbent under transient variable temperature conditions in fixed adsorption beds.

Effect of ceria surface facet on stability and reactivity of isolated platinum atoms

Well-defined surface structures and uniformity are key factors in exploring structure–activity relationships in heterogeneous catalysts.A modified atomic layer deposition method and three well-defined CeO_(2) nanoshapes,octahedra with(111)surfaces,cubes exposing(100)facets,and rods with(100)and(110)surface facet terminations,were utilized to synthesize ultra-low loading Pt/CeO_(2) catalysts and allow investigations on the influence of ceria surface facet on isolated Pt species under reducing conditions.A mild reduction temperature(150℃)reduces the initial platinum ions present on the surfaces of the ceria support but preserves the isolated Pt atoms on all ceria surface facets.In contrast,a reduction temperature of 350°C,reveals very different interactions between the initial single Pt atoms and the various ceria surface facets,leading to dissimilar and nonuniform Pt ensembles on the three ceria shapes.To isolate facet dependent Pt–CeO_(2) interactions and avoid variations between Pt species,the Pt1/CeO_(2) catalysts after reduction at 150°C were subjected to CO oxidation conditions.The isolated Pt atoms on the CeO_(2) octahedra and cubes are less active in the CO oxidation reaction,compared with Pt on CeO_(2) rods.In the case of Pt on the CeO_(2) octahedra this is due to strongly bound CO blocking active sites together with a stable CeO_(2)(111)surface limiting the oxygen supply from the support.On the CeO_(2) cubes,some Pt is not available for reaction and CO is bound strongly on the available Pt species.In addition,the Pt catalysts supported on the CeO_(2) cubes are not stable with time on stream.The isolated Pt atoms on the CeO_(2) rods are considerably more active under these conditions and this is due to a weaker Pt–CO bond strength and more facile reverse oxygen spillover from the defect-rich(110)surfaces of the rods due to the lower energy of oxygen vacancy formation on this CeO_(2) surface.The Pt supported on the CeO_(2) rods is also remarkably stable with time on stream.This work demonstrates the importance of using ultra-low loadings of active metal and well-defined oxide supports to isolate interactions between single metal atoms and oxide supports and determine the effects of the oxide support surface facet on the active metal at the atomic level.

The effect of gas phase polydimethylsiloxane surface treatment of metallic aluminum particles： Surface characterization and flow behavior

Aluminum particles were exposed to gaseous polydimethylsiloxane （PDMS） to produce a hydropho- bic surface coating for enhanced flow and fluidity. Surface retention of the intact PDMS was confirmed through infrared and X-ray photoelectron spectroscopy. Transmission electron microscopy was used to image cross-sections of the treated particles and energy dispersive spectroscopy element maps demon- strated the presence of a surface layer consisting of silicon and oxygen. Density measurements provided evidence for improvements in the Hausner ratio and Carr index of the PDMS-treated aluminum, indicating a reduction in inter-particulate cohesion through increased bulk density. Stability, compressibility, shear, aeration, and permeability of the particles were assessed by powder rheometer. The compressibility was reduced by approximately 32% following surface treatment, revealing a reduction in void space, while Mohr＇s circle analysis and shear testing determined that the extrapolated cohesion value was reduced by approximately 53% and the flow factor at 6 kPa was doubled. Aeration testing showed that the air velocity required to obtain a fluidized bed was on the order of 0.35 mm/s for the treated powder, whereas the raw powder could not be uniformly fluidized. PDMS may be a viable option for the large-scale treatment of aluminum powder for flow applications.