A kind of Ni-Cr-Fe-B-Si system amorphous alloy was used as interlayer in transient liquid-phase bonding(TLP bonding)of polycrystalline superalloy K465.The bonding behavior,microstructure feature and the tensile proper...A kind of Ni-Cr-Fe-B-Si system amorphous alloy was used as interlayer in transient liquid-phase bonding(TLP bonding)of polycrystalline superalloy K465.The bonding behavior,microstructure feature and the tensile properties of the joints were investigated.There are B-rich phase and Si-rich phase formed in the center of the seam after bonding at 1210℃for 30 min.The isothermal solidification is complete after bonding at 1210℃for 4 h.The relationship of the average width of the remnant eutectic zone and bonding time at 1210℃is nonlinear.The tensile strength of the bonded joint at room temperature and 900℃is comparable to that of K465 alloy.展开更多
With the use of Ti/Ni/Cu/Ni multiple foils as interlayer,carbon/carbon（C/C） composite was bonded to Nibased superalloy GH3044 by partial transient liquid-phase bonding technique.The effect of bonding temperature on ...With the use of Ti/Ni/Cu/Ni multiple foils as interlayer,carbon/carbon（C/C） composite was bonded to Nibased superalloy GH3044 by partial transient liquid-phase bonding technique.The effect of bonding temperature on the microstructures and strengths of the joints was investigated.The results showed that gradient structural multiple interlayers composed of ‘‘C–Ti reaction layer/Ti–Ni intermetallic compound layer/Ni–Cu sosoloid/residual Cu layer/Ni-GH3044 diffusion layer＇＇ were formed between C/C composite and GH3044.The shear strength of the C/C composite/GH3044 joint reached the highest value of 26.1 MPa when the bonding temperature was 1,030 °C.In addition,the fracture morphology showed that the fracture mode changed with the increase of bonding temperature.展开更多
Effect of holding time on microstructural developments and transformation of precipitates formed at the interface during transient liquid-phase bonding of a duplex stainless steel using a Ni-based amorphous insert all...Effect of holding time on microstructural developments and transformation of precipitates formed at the interface during transient liquid-phase bonding of a duplex stainless steel using a Ni-based amorphous insert alloy was studied. The experimental results reveal that the microstructure of the adjacent base metal varies clearly as a function of holding time. The migration of Cr and Ni elements and the → transformation seem to play relevant roles in this microstructure evolution. The scanning electron microscopy (SEM) and electron prob X-ray microanalysis (EPMA) results indicate the transformation of BN→BN and (N, Mo) boride→BN at the interface with the holding time of 60-1 800 s. N content changes with holding time increasing at locations at the interface might be a controlling factor contributing to this transformation.展开更多
The interfacial reactions in partial transient liquid-phase bonding of Si3N4 ceramics with Ti/Ni/Ti interlayers were studied by means of scanning electron microscopy （SEM）, energy dispersive spectrometry （EDS） and...The interfacial reactions in partial transient liquid-phase bonding of Si3N4 ceramics with Ti/Ni/Ti interlayers were studied by means of scanning electron microscopy （SEM）, energy dispersive spectrometry （EDS） and X-ray diffractometry （XRD）. It was shown that the interfacial structure of Si3N4/TiN/Ti5Si3+Ti5Si4 + Ni3Si/ （NiTi ） /Ni3Ti/ Ni was formed after bonding. The activation energies for TiN layer and the mixed reaction layer of Ti5Si3 + Ti5Si4 + Ni3Si are 546. 8 kJ/mol and 543. 9 kJ/mol, respectively. The formation and transition processes of interface layer sequence in the joint were clarified by diffusion path. An important characteristic, which is different from the conventional brazing and soid-state diffusion bonding, has been found, i. e., during the partial transient liquid-phase bonding, not only the reaction layers which have formed grow, but also the diffusion path in the subsequent reaction changes because of the remarkable variation of the concentration on the metal side.展开更多
Effects of the main process parameters（temperature and time） on microstructure and properties of Ti（C, N）/Ni interface bonded by （Cu＋Nb） interlayer in a vacuum diffusion bonding device were investigated. The in...Effects of the main process parameters（temperature and time） on microstructure and properties of Ti（C, N）/Ni interface bonded by （Cu＋Nb） interlayer in a vacuum diffusion bonding device were investigated. The interfacial microstructures consisted initially of Ni3Nb metallic compound and eutectic of Ni3Nb ＋ CuNiss, and finally transformed to （Ti, Nb） （C, N）＋Ni3Nb near Ti （C, N） and NiCuss ＋ Ni3Nb near Ni when diffusion bonding temperature was 1 523-1 573 K. It was clear that Cu was a constituent in the transient liquid phase （TLP） into which Ni was dissolved by forming Cu-Ni transition liquid. Nb was dissolved in Cu-Ni transition liquid rapidly. Ti （C, N） conld be wetted by resultant Ni-Nb-Cu transient liquid phase which was followed by a little （Ti, Nb） （C, N） solid solution formed at interface. This increased the interface combining capability. Ultimately the interface shear strength was able to reach 140 MPa. The theoretle analysis and experimental results show that the growth of interfacial reaction layer Ni3Nb accords with parabola law, and the activation energy of diffusion reaction is 115.0±0.5 kJ/mol, while the diffusion reaction speed constant is 12.53 mm/s^1/2.展开更多
In reactive-hot-pressed ZrB_(2)-SiC-ZrC ceramics,ZrO_(2) was found to replace ZrC phase,hence leading to confusion in designing ultra-high-temperature ceramics(UHTCs).We employ high-precision X-ray diffraction and ele...In reactive-hot-pressed ZrB_(2)-SiC-ZrC ceramics,ZrO_(2) was found to replace ZrC phase,hence leading to confusion in designing ultra-high-temperature ceramics(UHTCs).We employ high-precision X-ray diffraction and electron microscopies to reassess the phase behavior during entire reaction and densification and to reveal the evolution of multiphase relationship at different stages before reaching the final ZrB2-SiC-ZrO_(2) composition.Frozen from transient liquid-phase,bulk glassy phase of 15 vol% was found to be constituted of Zr-Si-B-C-O with stable Zr:O ratio,which starts as early as in the intermediate stage to suppress ZrC in favor of SiC nucleation.Inhomogeneity in phase relations and microstructures results from variation in local transient liquid-phase to develop SiC phase in various modes and rates.As inferred from the earlier report of phase formation,competing reactions for ZrC and ZrB_(2) phases in the initial stage below 1000℃ were mediated via Zr-O-B-C liquid phase.Such liquid phase was moderated by stable B-O components,as initiated from surface oxides of starting powders.This picture under a continuous mother liquid phase can unify the reactions and sintering into a collective meltingenucleationegrowth process,which enables and guides the evolution of multiphase relationship through several stages to reach final densification at relatively low temperature with the help of residual oxides.展开更多
Partial transient liquid phase （PTLP） bonding of TiC cermet to 06Cr19Ni10 stainless steel was carried out. Impulse pressuring was used to reduce the bonding time, and a Ti/Cu/Nb interlayer was employed to alleviate ...Partial transient liquid phase （PTLP） bonding of TiC cermet to 06Cr19Ni10 stainless steel was carried out. Impulse pressuring was used to reduce the bonding time, and a Ti/Cu/Nb interlayer was employed to alleviate the detrimental effect of interfacial reaction products on the bonding strength. Successful bonding was achieved at 885℃ under a pulsed pressure of 2-10 MPa within durations in the range of 2-8 min, which was notably shortened in comparison with conventional PTLP bonding. Microstructure characterization revealed the o- phase with a limit solubility of Nb, a sequence of Ti-Cu intermetallic phases and solid solutions of Ni and Cu in α＋β Ti in the reaction zone. The maximum shear strength of 106.7 MPa was obtained when the joint was bonded for 5 rain, indicating that a robust metallurgical bonding was achieved. Upon shear loading, the joints fractured along the Ti-Cu intermetallics interface and spread to the interior of TiC cermet in a brittle cleavage manner.展开更多
Genotyping by Target Sequencing(GBTS)technology,known for its flexibility,high efficiency,high throughput,and low cost,has been increasingly employed in molecular breeding.However,there is still limited study on the d...Genotyping by Target Sequencing(GBTS)technology,known for its flexibility,high efficiency,high throughput,and low cost,has been increasingly employed in molecular breeding.However,there is still limited study on the design and development of high-throughput genotyping tools in watermelon.In this study,we identified 112000 high quality SNPs by analyzing the resequencing data of 43 cultivated watermelon accessions.11921 and 6094 SNPs were selected for developing two sets of watermelon liquid-phase chips with different marker densities,named Watermelon 10K and 5K,respectively.Furthermore,the SNPs and Indels of most mapped gene/QTLs for many agronomic important traits in watermelon were also integrated into the two chips for foreground selection.These chips have been tested using GBTS technology in various applications in watermelon.The genotyping of 76 accessions by Watermelon 5K liquid-phase chip showed an average detection rate of 99.28%and 81.78%for cultivated and wild watermelon accessions,respectively.This provided enough markers information for GWAS and two significant QTLs,ssc1.1 and ssc1.2,associated with soluble sugar content were detected.Furthermore,BSA-seq analysis for non-lobed leaf and dwarf traits were validated by liquid-phase chips,and the candidate region was consistent with our previous studies.Additionally,we precisely introduced the Cldw1 and Clbl genes into an elite inbred line WT2 using Watermelon 5K for assisted selection,resulting in the development of three new germplasm with good plant architecture.As a high-throughput genotyping liquid-phase SNP array,the Watermelon 10K and 5K chips will greatly facilitate functional studies and molecular breeding in watermelon.展开更多
A comprehensive understanding of the structure and dynamic evolution of catalytic active sites is vital for advancing the study of liquid-phase acetylene hydrochlorination.Here,we successfully developed a Ru-DIPEA/TMS...A comprehensive understanding of the structure and dynamic evolution of catalytic active sites is vital for advancing the study of liquid-phase acetylene hydrochlorination.Here,we successfully developed a Ru-DIPEA/TMS catalyst optimised through systematic composition and condition tuning,demonstrating exceptional performance with 95.5%C_(2)H_(2)conversion and sustaining over 91.1%activity along with nearly 100%selectivity for VCM during a continuous 900-h test.Using a combination of characterisation techniques,including UV–vis spectroscopy,FT-IR spectroscopy,X-ray photoelectron spectroscopy,singlecrystal X-ray diffraction,and X-ray absorption spectroscopy,along with density functional theory(DFT)calculations,the structure and dynamic behaviour of the active sites were thoroughly investigated under the synergistic influence of ligands and HCl.The results revealed that HCl activation induces a significant structural transformation of the active sites,leading to the formation of a hexacoordinate complex,Ru(CO)_(2)C_(12)(C_(6)H_(15)N·HCl)_(2).DFT calculations further elucidated the mechanism underlying active site formation,revealing that an increased electron density around the Ru centre and corresponding changes in its coordination environment play critical roles in enhancing catalyst stability and activity.This study contributes to a deeper understanding of the structural basis of active site evolution during acetylene hydrochlorination,offering both practical insights into industrial applications and foundational knowledge for advancing liquid-phase catalysis.展开更多
Pt nanoparticles entrapped in ordered mesoporous CMK-3 carbons with p6mm symmetry were prepared using a facile impregnation method, and the resulting materials were characterized using X-ray diffraction spectroscopy, ...Pt nanoparticles entrapped in ordered mesoporous CMK-3 carbons with p6mm symmetry were prepared using a facile impregnation method, and the resulting materials were characterized using X-ray diffraction spectroscopy, N2 adsorption-desorption, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. The Pt nanoparticles were highly dispersed in the CMK-3 with 43.7% dispersion. The Pt/CMK-3 catalyst was an effective catalyst for the liquid-phase hydrogenation of nitrobenzene and its derivatives under the experimental conditions studied here. The Pt/CMK-3 catalyst was more active than commercial Pt/C catalyst in most cases. A highest turnover frequency of 43.8 s-1 was measured when the Pt/CMK-3 catalyst was applied for the hydrogenation of 2-methyl-nitrobenzene in ethanol under optimal conditions. It is worthy of note that the Pt/CMK-3 catalyst could be recycled easily, and could be reused at least fourteen times without any loss in activity or selectivity for the hydrogenation of nitrobenzene in ethanol.展开更多
Liquid phase oxidation of toluene is an environmental benign route for the production of benzoic acid.In a φ48mm bubble column reactor,the commercial process of toluene liquid phase oxidation was conducted with Co(CH...Liquid phase oxidation of toluene is an environmental benign route for the production of benzoic acid.In a φ48mm bubble column reactor,the commercial process of toluene liquid phase oxidation was conducted with Co(CH3COO)2.4H2O as catalyst.The Co2+ concentration [Co2+] was determined by extraction spectrophotometry and hereby the Co3+ concentration [Co3+] was obtained by mass balance.The results showed that [Co3+] reached the maximum at about 25-30min.[Co3+] increased with increasing Co catalyst amount at total Co concentration<150 mg.L-1 of toluene.The conversion of toluene,yield and selectivity of benzoic acid increased with the increasing [Co3+/Co2+] max.A high [Co3+] and a high [Co3+]/[Co2+] ratio are beneficial to the reaction.展开更多
The homogeneous liquid was separated into two phases, （Fe, Co）-rich LI and Cu-rich L2, once the melt was undercooled below a liquid-phase separation temperature Tsep. If the duration from Tsep to Tsl （solidificatio...The homogeneous liquid was separated into two phases, （Fe, Co）-rich LI and Cu-rich L2, once the melt was undercooled below a liquid-phase separation temperature Tsep. If the duration from Tsep to Tsl （solidification temperature of LI phase）, termed the liquid-phase separation interval Δt, exceeded a critical value, an eggtype structure was observed. By utilizing differential thermal analyses （DTA）, the solidification process of the undercooled Fe-Co-Cu alloys was studied. Additionally, an immiscible boundary was obtained, which was a convex parabola with a symmetrical axis of XCu=0.52. Depending on the relative amounts of LI and L2, the minor phase was nucleated firstly to form liquid droplets and separated from the original liquids at the beginning of liquid-phase separation.展开更多
The liquid-phase furfural （FAL） hydrogenation to furfuryl alcohol （FOL） and tetrahydrofurfuryl alcohol （THFOL） was investigated using sulfonate group （-SO3H） grafted activated carbon （AC） supported Ni cataly...The liquid-phase furfural （FAL） hydrogenation to furfuryl alcohol （FOL） and tetrahydrofurfuryl alcohol （THFOL） was investigated using sulfonate group （-SO3H） grafted activated carbon （AC） supported Ni catalyst, which was prepared and activated simultaneously by liquid phase reduction method. This functionalized nickel catalyst demonstrated an enhanced catalytic performance for selective hydrogenation of FAL, in which almost 100% FOL （〈80℃） and THFOL （〉100℃） selectivity with complete conversion was obtained, respectively. More importantly, the conversion of transfer hydrogenation of FAL to FOL also can reach almost 100% under optimal conditions （140℃, 4.0h）. The effect of -SO3H was evaluated and systematically analyzed by the combination of reaction performance and physico-chemical characterizations. Cycling test proved the prepared catalyst could be recycled and reused for several times without noticeably reducing catalytic activity of hvdrogenation.展开更多
The kinetics of liquid-phase hydrogenation of toluene catalyzed by MlNi_5 was studied by investigating the influences of the reaction temperature and pressure on the mass transfer-reaction processes inside the slurry....The kinetics of liquid-phase hydrogenation of toluene catalyzed by MlNi_5 was studied by investigating the influences of the reaction temperature and pressure on the mass transfer-reaction processes inside the slurry. The results show that the reaction rate accelerates when the reaction temperature increases, and reaches its maximum at about 490 K, but if temperature is higher than 510 K, the reaction rate decreases rapidly. The whole reaction process is controlled by the reaction at the surface of the catalyst particles. The mass transfer resistance at gas-liquid interface and that from the bulk liquid phase to the surface of the catalyst particle can be neglected. The apparent reaction rate is zero order for toluene concentration and first order for hydrogen concentration in the liquid phase. The kinetic model is obtained. The kinetic model fits the experimental data very well. The apparent activation energy of the hydrogen absorption reaction of MlNi_5-toluene slurry system is 41.01 kJ·mol^(-1).展开更多
The main problems with the liquid-phase technology of carbon fiber/aluminum matrix composites include poor wetting of the fiber with liquid aluminum and formation of aluminum carbide on the fibers’surface.This paper ...The main problems with the liquid-phase technology of carbon fiber/aluminum matrix composites include poor wetting of the fiber with liquid aluminum and formation of aluminum carbide on the fibers’surface.This paper aims to solve these problems.The theoretical and experimental dependence of porosity on the applied pressure were determined.The possibility of obtaining a carbon fiber/aluminum matrix composite wire with a strength value of about 1500 MPa was shown.The correlation among the strength of the carbon fiber reinforced aluminum matrix composite,the fracture surface,and the degradation of the carbon fiber surface was discussed.展开更多
Cu-Zn-Al slurry catalysts were prepared using a complete liquid-phase preparation technology under different heat treatment atmospheres.The catalysts were characterized using X-ray diffraction,X-ray photoelectron spec...Cu-Zn-Al slurry catalysts were prepared using a complete liquid-phase preparation technology under different heat treatment atmospheres.The catalysts were characterized using X-ray diffraction,X-ray photoelectron spectroscope,and N2 adsorption-desorption.Their application in the single-step synthesis of dimethyl ether from syngas was also investigated.The results indicate that the type of heat treatment atmosphere has an influence on the Cu species and the Cu0/Cu＋ ratio on the catalyst surface.Moreover,the final Cu/Zn ratio on the catalyst surface is mainly dependent on the composition and reaction environment of the catalyst and less on the type of heat treatment atmosphere.The prepared catalysts can suppress sintering of active sites at high temperatures,and the type of heat treatment atmosphere mainly affects the capability of the catalyst for methanol synthesis.The catalysts perform best using N2 as the heat treatment atmosphere.展开更多
TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, s...TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, field emission scanning electron microscopy （FE- SEM）, transmission electron microscopy （TEM）, and selected area electron diffraction （SAED） analysis. Results of electron microscopic observations indicated that the nanowires were smooth and uniform with a diameter of about 50-80 nm and several micrometers in length. SAED, Raman, and XRD mea- surements showed that TiO2 nanowires were single-crystalline with a pure rutile structure after heating at 800 ~C for 10 h. In this situation, the nanowire constituents grew preferentially along the 〈001〉 direction. Furthermore, the formation process and mechanistic study of the Ti02 nanowire arrays were proposed and discussed in detail. The nanowires are clearly produced by the deposition of TiO2 particles on the inner wall of the template nanochannels.展开更多
According to the characteristics of FCC diesel, a technology of liquid-phase hydrodesulfurization of the diesel in tubular reactors was proposed and lab-scale experiments were carried out. A kinetic model for the hydr...According to the characteristics of FCC diesel, a technology of liquid-phase hydrodesulfurization of the diesel in tubular reactors was proposed and lab-scale experiments were carried out. A kinetic model for the hydrodesulfurization process was developed and verified. The model was utilized to predict the sulfur content of products under different operating conditions. The effects of temperature, space velocity, pressure, and hydrogen concentration on the dcsulfurization rate were investigated.展开更多
Olivine LiFePO4/C nanowires have been successfully synthesized by a simple and eco-friendly solution preparation.The phase,structure,morphology and composition of the as-prepared products were characterized by powder ...Olivine LiFePO4/C nanowires have been successfully synthesized by a simple and eco-friendly solution preparation.The phase,structure,morphology and composition of the as-prepared products were characterized by powder X-ray diffraction(XRD),scanning electron microscopy(SEM),thermogravimetric and differential-thermogravimetric analysis(TG-DTA) and energy dispersive X-ray spectrometry(EDS) techniques,showing uniform nanowire shape of LiFePO4/C with a diameter of 80-150 nm and a length of several microns.The heat-treated LiFePO4/C nanowires show excellent electrochemical properties of specific discharge capacity,rate capacity and cycling stability.In particular,the LiFePO4/C nanowires heat-treated at 400 °C show preferable first discharge specific capacity of 161 mA·h/g at 0.1C rate,while the voltage platform is 3.4 V and the first discharge specific capacity is 93 mA·h/g at 20C rate.The specific capacity retention is 98% after 50 cycles at 5C rate.展开更多
Nanobubbles have attracted considerable attention in various industrial applications due to their exceptionally long lifetime and their potential as carriers at the nanoscale.The stability and physiochemical propertie...Nanobubbles have attracted considerable attention in various industrial applications due to their exceptionally long lifetime and their potential as carriers at the nanoscale.The stability and physiochemical properties of nanobubbles are highly sensitive to the presence of surfactants that can lower their surface tension or improve their electrostatic stabilization.Herein,we report real-time observations of the dynamic behaviors of nanobubbles in the presence of soluble surfactants.Using liquid-phase transmission electron microscopy(TEM)with multi-chamber graphene liquid cells,bulk nanobubbles and surface nanobubbles were observed in the same imaging condition.Our direct observations of nanobubbles indicate that stable gas transport frequently occurs without interfaces merging,while a narrow distance is maintained between the interfaces of interacting surfactant-laden nanobubbles.Our results also elucidate that the interface curvature of nanobubbles is an important factor that determines their interfacial stability.展开更多
基金financially supported by the National Basic Research Program China(Nos.2010CB631200 and 2010CB631206)the National Natural Science Foundation of China(Nos.50971124,50904059,51071165,U1037601 and 51204156)
文摘A kind of Ni-Cr-Fe-B-Si system amorphous alloy was used as interlayer in transient liquid-phase bonding(TLP bonding)of polycrystalline superalloy K465.The bonding behavior,microstructure feature and the tensile properties of the joints were investigated.There are B-rich phase and Si-rich phase formed in the center of the seam after bonding at 1210℃for 30 min.The isothermal solidification is complete after bonding at 1210℃for 4 h.The relationship of the average width of the remnant eutectic zone and bonding time at 1210℃is nonlinear.The tensile strength of the bonded joint at room temperature and 900℃is comparable to that of K465 alloy.
基金financially supported by the National Natural Science Foundation of China(Nos.51202193 and 51221001)the Fundamental Research Foundation of Northwestern Polytechnical University(No.GBKY1021)the‘‘111’’Project(No.08040)
文摘With the use of Ti/Ni/Cu/Ni multiple foils as interlayer,carbon/carbon（C/C） composite was bonded to Nibased superalloy GH3044 by partial transient liquid-phase bonding technique.The effect of bonding temperature on the microstructures and strengths of the joints was investigated.The results showed that gradient structural multiple interlayers composed of ‘‘C–Ti reaction layer/Ti–Ni intermetallic compound layer/Ni–Cu sosoloid/residual Cu layer/Ni-GH3044 diffusion layer＇＇ were formed between C/C composite and GH3044.The shear strength of the C/C composite/GH3044 joint reached the highest value of 26.1 MPa when the bonding temperature was 1,030 °C.In addition,the fracture morphology showed that the fracture mode changed with the increase of bonding temperature.
基金Project(51205428) supported by the National Natural Science Foundation of ChinaProject(CDJRC10130011) supported by the Fundamental Research Funds for the Central Universities, ChinaProject(2010-0001-222) supported by NCRC (National Core Research Center) Program through the National Research Foundation of Korea funded by the Ministry of Education, Science and Technology,Korea
文摘Effect of holding time on microstructural developments and transformation of precipitates formed at the interface during transient liquid-phase bonding of a duplex stainless steel using a Ni-based amorphous insert alloy was studied. The experimental results reveal that the microstructure of the adjacent base metal varies clearly as a function of holding time. The migration of Cr and Ni elements and the → transformation seem to play relevant roles in this microstructure evolution. The scanning electron microscopy (SEM) and electron prob X-ray microanalysis (EPMA) results indicate the transformation of BN→BN and (N, Mo) boride→BN at the interface with the holding time of 60-1 800 s. N content changes with holding time increasing at locations at the interface might be a controlling factor contributing to this transformation.
文摘The interfacial reactions in partial transient liquid-phase bonding of Si3N4 ceramics with Ti/Ni/Ti interlayers were studied by means of scanning electron microscopy （SEM）, energy dispersive spectrometry （EDS） and X-ray diffractometry （XRD）. It was shown that the interfacial structure of Si3N4/TiN/Ti5Si3+Ti5Si4 + Ni3Si/ （NiTi ） /Ni3Ti/ Ni was formed after bonding. The activation energies for TiN layer and the mixed reaction layer of Ti5Si3 + Ti5Si4 + Ni3Si are 546. 8 kJ/mol and 543. 9 kJ/mol, respectively. The formation and transition processes of interface layer sequence in the joint were clarified by diffusion path. An important characteristic, which is different from the conventional brazing and soid-state diffusion bonding, has been found, i. e., during the partial transient liquid-phase bonding, not only the reaction layers which have formed grow, but also the diffusion path in the subsequent reaction changes because of the remarkable variation of the concentration on the metal side.
基金Funded by the National Natural Science Foundation of China (No.50074017/E0408)
文摘Effects of the main process parameters（temperature and time） on microstructure and properties of Ti（C, N）/Ni interface bonded by （Cu＋Nb） interlayer in a vacuum diffusion bonding device were investigated. The interfacial microstructures consisted initially of Ni3Nb metallic compound and eutectic of Ni3Nb ＋ CuNiss, and finally transformed to （Ti, Nb） （C, N）＋Ni3Nb near Ti （C, N） and NiCuss ＋ Ni3Nb near Ni when diffusion bonding temperature was 1 523-1 573 K. It was clear that Cu was a constituent in the transient liquid phase （TLP） into which Ni was dissolved by forming Cu-Ni transition liquid. Nb was dissolved in Cu-Ni transition liquid rapidly. Ti （C, N） conld be wetted by resultant Ni-Nb-Cu transient liquid phase which was followed by a little （Ti, Nb） （C, N） solid solution formed at interface. This increased the interface combining capability. Ultimately the interface shear strength was able to reach 140 MPa. The theoretle analysis and experimental results show that the growth of interfacial reaction layer Ni3Nb accords with parabola law, and the activation energy of diffusion reaction is 115.0±0.5 kJ/mol, while the diffusion reaction speed constant is 12.53 mm/s^1/2.
基金financially supported by the National Natural Science Foundation of China(No.51532006)the Shanghai Municipal Science and Technology Commission(No.16DZ2260600)the 111 Project of the Ministry of Education and the National Bureau of Foreign Experts(No.D16002).
文摘In reactive-hot-pressed ZrB_(2)-SiC-ZrC ceramics,ZrO_(2) was found to replace ZrC phase,hence leading to confusion in designing ultra-high-temperature ceramics(UHTCs).We employ high-precision X-ray diffraction and electron microscopies to reassess the phase behavior during entire reaction and densification and to reveal the evolution of multiphase relationship at different stages before reaching the final ZrB2-SiC-ZrO_(2) composition.Frozen from transient liquid-phase,bulk glassy phase of 15 vol% was found to be constituted of Zr-Si-B-C-O with stable Zr:O ratio,which starts as early as in the intermediate stage to suppress ZrC in favor of SiC nucleation.Inhomogeneity in phase relations and microstructures results from variation in local transient liquid-phase to develop SiC phase in various modes and rates.As inferred from the earlier report of phase formation,competing reactions for ZrC and ZrB_(2) phases in the initial stage below 1000℃ were mediated via Zr-O-B-C liquid phase.Such liquid phase was moderated by stable B-O components,as initiated from surface oxides of starting powders.This picture under a continuous mother liquid phase can unify the reactions and sintering into a collective meltingenucleationegrowth process,which enables and guides the evolution of multiphase relationship through several stages to reach final densification at relatively low temperature with the help of residual oxides.
基金Project(51421001)supported by the National Natural Science Foundation of ChinaProjects(106112015CDJXZ138803,106112015CDJXY130003)supported by the Fundamental Research Funds for the Central Universities,China
文摘Partial transient liquid phase （PTLP） bonding of TiC cermet to 06Cr19Ni10 stainless steel was carried out. Impulse pressuring was used to reduce the bonding time, and a Ti/Cu/Nb interlayer was employed to alleviate the detrimental effect of interfacial reaction products on the bonding strength. Successful bonding was achieved at 885℃ under a pulsed pressure of 2-10 MPa within durations in the range of 2-8 min, which was notably shortened in comparison with conventional PTLP bonding. Microstructure characterization revealed the o- phase with a limit solubility of Nb, a sequence of Ti-Cu intermetallic phases and solid solutions of Ni and Cu in α＋β Ti in the reaction zone. The maximum shear strength of 106.7 MPa was obtained when the joint was bonded for 5 rain, indicating that a robust metallurgical bonding was achieved. Upon shear loading, the joints fractured along the Ti-Cu intermetallics interface and spread to the interior of TiC cermet in a brittle cleavage manner.
基金supported by the National Natural Science Foundation of China(Grant Nos.32172602,32472739)the Major Science and Technology Project of Henan Province(Grant No.221100110400)+3 种基金the Funding of Joint Research on Agricultural Varietie Improvement of Henan Province(Grant No.2022010503)the Natural Science Foundation of Henan(Grant No.242300421030)the Key Scientifc and Technological Project of Henan Province(Grant Nos.242102111124,242102111115)the Key Research and Development Program of Xinjiang Uygur autonomous region(2023B02017-2).
文摘Genotyping by Target Sequencing(GBTS)technology,known for its flexibility,high efficiency,high throughput,and low cost,has been increasingly employed in molecular breeding.However,there is still limited study on the design and development of high-throughput genotyping tools in watermelon.In this study,we identified 112000 high quality SNPs by analyzing the resequencing data of 43 cultivated watermelon accessions.11921 and 6094 SNPs were selected for developing two sets of watermelon liquid-phase chips with different marker densities,named Watermelon 10K and 5K,respectively.Furthermore,the SNPs and Indels of most mapped gene/QTLs for many agronomic important traits in watermelon were also integrated into the two chips for foreground selection.These chips have been tested using GBTS technology in various applications in watermelon.The genotyping of 76 accessions by Watermelon 5K liquid-phase chip showed an average detection rate of 99.28%and 81.78%for cultivated and wild watermelon accessions,respectively.This provided enough markers information for GWAS and two significant QTLs,ssc1.1 and ssc1.2,associated with soluble sugar content were detected.Furthermore,BSA-seq analysis for non-lobed leaf and dwarf traits were validated by liquid-phase chips,and the candidate region was consistent with our previous studies.Additionally,we precisely introduced the Cldw1 and Clbl genes into an elite inbred line WT2 using Watermelon 5K for assisted selection,resulting in the development of three new germplasm with good plant architecture.As a high-throughput genotyping liquid-phase SNP array,the Watermelon 10K and 5K chips will greatly facilitate functional studies and molecular breeding in watermelon.
基金supported by the National Natural Science Foundation of China(No.22378308)Jing-Jin-Ji Regional Integrated Environmental Improvement-National Science and Technology Major Project(No.2024ZD1200301–2)the Scientific and Technological Project of Yunnan Precious Metal Laboratory(No.YPML2023050202)。
文摘A comprehensive understanding of the structure and dynamic evolution of catalytic active sites is vital for advancing the study of liquid-phase acetylene hydrochlorination.Here,we successfully developed a Ru-DIPEA/TMS catalyst optimised through systematic composition and condition tuning,demonstrating exceptional performance with 95.5%C_(2)H_(2)conversion and sustaining over 91.1%activity along with nearly 100%selectivity for VCM during a continuous 900-h test.Using a combination of characterisation techniques,including UV–vis spectroscopy,FT-IR spectroscopy,X-ray photoelectron spectroscopy,singlecrystal X-ray diffraction,and X-ray absorption spectroscopy,along with density functional theory(DFT)calculations,the structure and dynamic behaviour of the active sites were thoroughly investigated under the synergistic influence of ligands and HCl.The results revealed that HCl activation induces a significant structural transformation of the active sites,leading to the formation of a hexacoordinate complex,Ru(CO)_(2)C_(12)(C_(6)H_(15)N·HCl)_(2).DFT calculations further elucidated the mechanism underlying active site formation,revealing that an increased electron density around the Ru centre and corresponding changes in its coordination environment play critical roles in enhancing catalyst stability and activity.This study contributes to a deeper understanding of the structural basis of active site evolution during acetylene hydrochlorination,offering both practical insights into industrial applications and foundational knowledge for advancing liquid-phase catalysis.
基金supported by the National Natural Science Foundation of China(21273076 and 21373089)the Open Research Fund of Top Key Discipline of Chemistry in Zhejiang Provincial Colleges and Key Laboratory of the Ministry of Education for Catalysis Materials(Zhejiang Normal University,ZJHX2013)Shanghai Leading Academic Discipline Project (B409)~~
文摘Pt nanoparticles entrapped in ordered mesoporous CMK-3 carbons with p6mm symmetry were prepared using a facile impregnation method, and the resulting materials were characterized using X-ray diffraction spectroscopy, N2 adsorption-desorption, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. The Pt nanoparticles were highly dispersed in the CMK-3 with 43.7% dispersion. The Pt/CMK-3 catalyst was an effective catalyst for the liquid-phase hydrogenation of nitrobenzene and its derivatives under the experimental conditions studied here. The Pt/CMK-3 catalyst was more active than commercial Pt/C catalyst in most cases. A highest turnover frequency of 43.8 s-1 was measured when the Pt/CMK-3 catalyst was applied for the hydrogenation of 2-methyl-nitrobenzene in ethanol under optimal conditions. It is worthy of note that the Pt/CMK-3 catalyst could be recycled easily, and could be reused at least fourteen times without any loss in activity or selectivity for the hydrogenation of nitrobenzene in ethanol.
基金Supported by the National Natural Science Foundation of China （20576081, 20736009） and the Ph.D. Programs Foundation of Ministry of Education of China （20070610128）.
文摘Liquid phase oxidation of toluene is an environmental benign route for the production of benzoic acid.In a φ48mm bubble column reactor,the commercial process of toluene liquid phase oxidation was conducted with Co(CH3COO)2.4H2O as catalyst.The Co2+ concentration [Co2+] was determined by extraction spectrophotometry and hereby the Co3+ concentration [Co3+] was obtained by mass balance.The results showed that [Co3+] reached the maximum at about 25-30min.[Co3+] increased with increasing Co catalyst amount at total Co concentration<150 mg.L-1 of toluene.The conversion of toluene,yield and selectivity of benzoic acid increased with the increasing [Co3+/Co2+] max.A high [Co3+] and a high [Co3+]/[Co2+] ratio are beneficial to the reaction.
基金supported by the Natural Science Foundation of China (Grant No.50771084)the Natural Science Foundation of the Education Department of Jiangsu province,China (Grant No.09KJB430004)
文摘The homogeneous liquid was separated into two phases, （Fe, Co）-rich LI and Cu-rich L2, once the melt was undercooled below a liquid-phase separation temperature Tsep. If the duration from Tsep to Tsl （solidification temperature of LI phase）, termed the liquid-phase separation interval Δt, exceeded a critical value, an eggtype structure was observed. By utilizing differential thermal analyses （DTA）, the solidification process of the undercooled Fe-Co-Cu alloys was studied. Additionally, an immiscible boundary was obtained, which was a convex parabola with a symmetrical axis of XCu=0.52. Depending on the relative amounts of LI and L2, the minor phase was nucleated firstly to form liquid droplets and separated from the original liquids at the beginning of liquid-phase separation.
基金the National Natural Science Foundation of China (Nos. 51502297, 51372248, and 51432009)Instrument Developing Project of the Chinese Academy of Sciences (No. yz201421)
文摘The liquid-phase furfural （FAL） hydrogenation to furfuryl alcohol （FOL） and tetrahydrofurfuryl alcohol （THFOL） was investigated using sulfonate group （-SO3H） grafted activated carbon （AC） supported Ni catalyst, which was prepared and activated simultaneously by liquid phase reduction method. This functionalized nickel catalyst demonstrated an enhanced catalytic performance for selective hydrogenation of FAL, in which almost 100% FOL （〈80℃） and THFOL （〉100℃） selectivity with complete conversion was obtained, respectively. More importantly, the conversion of transfer hydrogenation of FAL to FOL also can reach almost 100% under optimal conditions （140℃, 4.0h）. The effect of -SO3H was evaluated and systematically analyzed by the combination of reaction performance and physico-chemical characterizations. Cycling test proved the prepared catalyst could be recycled and reused for several times without noticeably reducing catalytic activity of hvdrogenation.
文摘The kinetics of liquid-phase hydrogenation of toluene catalyzed by MlNi_5 was studied by investigating the influences of the reaction temperature and pressure on the mass transfer-reaction processes inside the slurry. The results show that the reaction rate accelerates when the reaction temperature increases, and reaches its maximum at about 490 K, but if temperature is higher than 510 K, the reaction rate decreases rapidly. The whole reaction process is controlled by the reaction at the surface of the catalyst particles. The mass transfer resistance at gas-liquid interface and that from the bulk liquid phase to the surface of the catalyst particle can be neglected. The apparent reaction rate is zero order for toluene concentration and first order for hydrogen concentration in the liquid phase. The kinetic model is obtained. The kinetic model fits the experimental data very well. The apparent activation energy of the hydrogen absorption reaction of MlNi_5-toluene slurry system is 41.01 kJ·mol^(-1).
基金financially supported by ISSP RAS-Russian Government contracts
文摘The main problems with the liquid-phase technology of carbon fiber/aluminum matrix composites include poor wetting of the fiber with liquid aluminum and formation of aluminum carbide on the fibers’surface.This paper aims to solve these problems.The theoretical and experimental dependence of porosity on the applied pressure were determined.The possibility of obtaining a carbon fiber/aluminum matrix composite wire with a strength value of about 1500 MPa was shown.The correlation among the strength of the carbon fiber reinforced aluminum matrix composite,the fracture surface,and the degradation of the carbon fiber surface was discussed.
基金supported by the National Natural Science Foundation of China(No.20706039)the National Basic Research Program(973 Program) of China (No.2005CB221204)+1 种基金the Program for the Top Young Academic Leaders of Higher Learning Institutions of Shanxi of China in 2010the Young Scientific and the Technical Fund of Shanxi of China (No.2006021010)
文摘Cu-Zn-Al slurry catalysts were prepared using a complete liquid-phase preparation technology under different heat treatment atmospheres.The catalysts were characterized using X-ray diffraction,X-ray photoelectron spectroscope,and N2 adsorption-desorption.Their application in the single-step synthesis of dimethyl ether from syngas was also investigated.The results indicate that the type of heat treatment atmosphere has an influence on the Cu species and the Cu0/Cu＋ ratio on the catalyst surface.Moreover,the final Cu/Zn ratio on the catalyst surface is mainly dependent on the composition and reaction environment of the catalyst and less on the type of heat treatment atmosphere.The prepared catalysts can suppress sintering of active sites at high temperatures,and the type of heat treatment atmosphere mainly affects the capability of the catalyst for methanol synthesis.The catalysts perform best using N2 as the heat treatment atmosphere.
基金supported by the Institute of Science and High Technology and Environmental Sciences(No.1/1859)
文摘TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, field emission scanning electron microscopy （FE- SEM）, transmission electron microscopy （TEM）, and selected area electron diffraction （SAED） analysis. Results of electron microscopic observations indicated that the nanowires were smooth and uniform with a diameter of about 50-80 nm and several micrometers in length. SAED, Raman, and XRD mea- surements showed that TiO2 nanowires were single-crystalline with a pure rutile structure after heating at 800 ~C for 10 h. In this situation, the nanowire constituents grew preferentially along the 〈001〉 direction. Furthermore, the formation process and mechanistic study of the Ti02 nanowire arrays were proposed and discussed in detail. The nanowires are clearly produced by the deposition of TiO2 particles on the inner wall of the template nanochannels.
基金the financial support from the SINOPEC(No.2014310031600599)
文摘According to the characteristics of FCC diesel, a technology of liquid-phase hydrodesulfurization of the diesel in tubular reactors was proposed and lab-scale experiments were carried out. A kinetic model for the hydrodesulfurization process was developed and verified. The model was utilized to predict the sulfur content of products under different operating conditions. The effects of temperature, space velocity, pressure, and hydrogen concentration on the dcsulfurization rate were investigated.
基金Project(51202066)supported by the National Natural Science Foundation of ChinaProject supported by Scientific Research Fund of Hunan Provincial Science and Technology Department,China+1 种基金Project(2013-26)supported by the State Key Program of Jilin University,ChinaProject(2013001)supported by Key Laboratory of Ecological Impacts of Hydraulic-projects and Restoration of Aquatic Ecosystem,Minister of Water Resources,China
文摘Olivine LiFePO4/C nanowires have been successfully synthesized by a simple and eco-friendly solution preparation.The phase,structure,morphology and composition of the as-prepared products were characterized by powder X-ray diffraction(XRD),scanning electron microscopy(SEM),thermogravimetric and differential-thermogravimetric analysis(TG-DTA) and energy dispersive X-ray spectrometry(EDS) techniques,showing uniform nanowire shape of LiFePO4/C with a diameter of 80-150 nm and a length of several microns.The heat-treated LiFePO4/C nanowires show excellent electrochemical properties of specific discharge capacity,rate capacity and cycling stability.In particular,the LiFePO4/C nanowires heat-treated at 400 °C show preferable first discharge specific capacity of 161 mA·h/g at 0.1C rate,while the voltage platform is 3.4 V and the first discharge specific capacity is 93 mA·h/g at 20C rate.The specific capacity retention is 98% after 50 cycles at 5C rate.
基金financial support from the National Research Foundation of Korea(NRF)grant funded by the Korean government(Ministry of Science and ICT,NRF-2017R1A5A1015365)Creative-Pioneering Researchers Program through Seoul National University(2020)+3 种基金the Interdisciplinary Research Initiatives Programs by College of Engineering and College of Medicine,Seoul National Universitythe POSCO Science Fellowship of POSCO TJ Park Foundationthe support from the NRF funded by the Ministry of Education(2019R1F1A1059099 and 2020R1F1A1065856)the support from the research fund of Hanyang University(HY-2018-N)。
文摘Nanobubbles have attracted considerable attention in various industrial applications due to their exceptionally long lifetime and their potential as carriers at the nanoscale.The stability and physiochemical properties of nanobubbles are highly sensitive to the presence of surfactants that can lower their surface tension or improve their electrostatic stabilization.Herein,we report real-time observations of the dynamic behaviors of nanobubbles in the presence of soluble surfactants.Using liquid-phase transmission electron microscopy(TEM)with multi-chamber graphene liquid cells,bulk nanobubbles and surface nanobubbles were observed in the same imaging condition.Our direct observations of nanobubbles indicate that stable gas transport frequently occurs without interfaces merging,while a narrow distance is maintained between the interfaces of interacting surfactant-laden nanobubbles.Our results also elucidate that the interface curvature of nanobubbles is an important factor that determines their interfacial stability.
