组合式H型钢门式支架施工技术在市政互通匝道桥施工中的应用

福州市福湾路提升改造工程,采用组合式H型钢现浇箱梁支架来解决上跨匝道桥和紧邻营运线桥梁施工中的上下空间受限和钢管支墩布跨过大的技术难题,可供类似桥梁施工借鉴。     

Albumin mediated reactive oxygen species scavenging and targeted delivery of methotrexate for rheumatoid arthritis therapy

Rheumatoid arthritis(RA)is a common chronic systemic autoimmune disease.Although there are a variety of treatments for RA,the substantial clinical therapies are still limited to disease-modifying anti-rheumatic drugs(DMARD),which would induce obvious side-effect in patients after long-term administration.Herein,an uncomplicated drug-induced self-assembly strategy was proposed to fabricate enzyme-loaded albumin nanomedicine.The hydrophobic drug methotrexate(MTX)could induce self-assembly of superoxide dismutase(SOD)and human serum albumin(HSA)to form HSA-SOD-MTX nanoparticle.After intravenous injection,dual-modal imaging including fluorescence imaging or single-photon emission computed tomography(SPECT)/CT imaging exhibits high accumulation of cyanine 5.5(Cy5.5)or 125l labeled HSA-SOD-MTX nanoparticles in the joints of collagen-induced arthritis(CIA)mice.Importantly,using the synergy therapy of SOD enzyme to scavenge the reactive oxygen species(ROS)and MTX to suppress inflammation,HSA-SOD-MTX nanoparticles exhibit excellent therapeutic efficiency of RA in CIA mice compared with the other groups.Micro-CT and clinical arthritis score of RA mice further demonstrate that RA symptoms of mice treated with HSA-SOD-MTX nanoparticles is significantly relived,which was further demonstrated by the histological analysis and the inflammatory factors measurement.The synergy therapy of inflammation by MTX and SOD enzyme based on HSA-SOD-MTX nanoparticles show excellent therapeutic effects of RA without inducing obvious side effects.Therefore,our strategy may further promote the highly efficient therapy of RA using SOD enzyme to scavenge the ROS and decreasing the side-effect of MTX,which may provide the reference for clinical RA treatment.     

Interfacial reaction between zirconium alloy and graphite mold/yttrium oxide ceramic mold

Zirconium alloys are active in the molten state and tend to react with the mold during casting. The casting technology of zirconium is not yet well established; especially in selecting the mold materials, which are difficult to determine. In the present work, the interfacial reactions between zirconium casting and casting mold were studied. The zirconium alloy was melted in a vacuum arc skull furnace and then cast into the graphite mold and ceramic mold, respectively. The zirconium casting samples were characterized using SEM, EDS and XRD with an emphasis on the chemical diffusion of elements. A reaction layer was observed at the casting surface. Chemical analysis shows that chemical elements C, O and Y from the mold are diffused into the molten zirconium, and new phases, such as ZrC, Zr30, YO1.335 and Y6ZrO11, are formed at the surface. In addition, an end product of zirconium valve cast in a yttria mold has a compact structure and good surface quality.     

Effects of laser shock processing,solid solution and aging,and cryogenic treatments on microstructure and thermal fatigue performance of ZCuAl10Fe3Mn2 alloy

The materials used in variable temperature conditions are required to have excellent thermal fatigue performance. The effects of laser shock processing (LSP), solid solution and aging treatment (T6), and cryogenic treatment (CT) on both microstructure and thermal fatigue performance of ZCuAl₁₀Fe₃Mn₂ alloys were studied. Microstructure and crack morphology were then examined by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The result showed that, after being subjected to the combination treatment of T6+CT+LSP, the optimal mechanical properties and thermal fatigue performance were obtained for the ZCuAl₁₀Fe₃Mn₂ alloy with the tensile strength, hardness, and elongation of 720 MPa, 300.16 HB, and 16%, respectively, and the thermal fatigue life could reach 7,100 cycles when the crack length was 0.1 mm. Moreover, the ZCuAl₁₀Fe₃Mn₂ after combination treatment shows high resistance to oxidation, good adhesion between the matrix and grain boundaries, and dramatically reduced growth rate of crack. During thermal fatigue testing, under the combined action of thermal and alternating stresses, the microstructure around the sample notch oxidized and became loose and porous, which then converted to micro-cracks. Fatigue crack expanded along the grain boundary in the early stage. In the later stage, under the cyclic stress accumulation, the oxidized microstructure separated from the matrix, and the fatigue crack expanded in both intergranular and transgranular ways. The main crack was thick, and the path was meandering.     

Additive manufacturing and foundry innovation

Additive manufacturing is expected to transform and upgrade the traditional foundry industry to realize the integrated manufacturing and rapid and low-cost development of high-performance components with complex shapes. The additive manufacturing technology commonly applied in casting mold preparation (fusible molds, sand molds/cores and ceramic cores) mainly includes selective laser sintering (SLS) and binder injection three-dimensional printing (3DP). In this work, the research status of SLS/3DP-casting processes on material preparation, equipment development, process optimization, simulation and application cases in aerospace, automotive and other fields were elaborated. Finally, the developing trends of the additive manufacturing technology in the future of foundry field are introduced, including multi-material sand molds (metal core included), ceramic core-shell integration and die-casting dies with conformal cooling runners.     

Microstructure and mechanical properties of laser additive manufactured novel titanium alloy after heat treatment

A novel α+β titanium alloy with multi-alloying addition was designed based on the cluster formula 12[Al-Ti₁₂](AlTi₂)+5[Al-Ti₁₄](AlV_1.2Mo_0.6Nb_0.2) which was derived from Ti-6Al-4V.The nominal composition of this novel alloy was determined as Ti-6.83Al-2.28V-2.14Mo-0.69Nb-6.79Zr.In this study,the novel alloy and Ti-6Al-4V alloy samples were prepared by laser additive manufacturing.The microstructure,micro-hardness,room/high temperature tensile properties of the as-deposited samples were investigated.Compared to Ti-6Al-4V,the novel alloy has much higher room and high temperature (600℃) tensile strengths,which are 1,427.5 MPa and 642.2 MPa,respectively;however,it has a much lower elongation (3.2%) at room temperature because of the finer microstructure.To improve the elongation of the novel alloy,heat treatment was used.After solution at 960℃ or 970℃ for 1 h followed by air cooling and aging at 550℃ for 4 h followed by air cooling,a unique bi-modal microstructure which contains crab-like primary α and residual β phase is obtained,improving the compression elongation by 80.9% compared to the as-deposited samples.The novel alloy can be used as a high-temperature and high-strength candidate for laser additive manufacturing.     

某深基坑中管井降水施工技术及监测维护措施探讨

本文根据工程中的深基坑开挖施工的要求,实施了管井降水的方法,从而达到了基坑降水的目的。通过对管井降水实施效果的分析,表明了该方法具有良好的效果。     

Carbon-coated Ni-Co alloy catalysts: preparation and performance for in-situ aqueous phase hydrodeoxygenation of methyl palmitate to hydrocarbons using methanol as the hydrogen donor

Carbon-coated Ni, Co and Ni-Co alloy catalysts were prepared by the carbonization of the metal doped resorcinol-formaldehyde resins synthesized by the one-pot extended Stöber method. It was found that the introduction of Co remarkably reduced the carbon microsphere size. The metallic Ni, Co, and Ni-Co alloy particles (mainly 10–12 nm) were uniformly distributed in carbon microspheres. A charge transfer from Ni to Co appeared in the Ni-Co alloy. Compared with those of metallic Ni and Co, the d-band center of the Ni-Co alloy shifted away from and toward the Fermi level, respectively. In the in-situ aqueous phase hydrodeoxygenation of methyl palmitate with methanol as the hydrogen donor at 330 °C, the decarbonylation/decarboxylation pathway dominated on all catalysts. The Ni-Co@C catalysts gave higher activity than the Ni@C and Co@C catalysts, and the yields of n-pentadecane and n-C₆–n-C₁₆ reached 71.6% and 92.6%, respectively. The excellent performance of Ni-Co@C is attributed to the electronic interactions between Ni and Co and the small carbon microspheres. Due to the confinement effect of carbon, the metal particles showed high resistance to sintering under harsh hydrothermal conditions. Catalyst deactivation is due to the carbonaceous deposition, and the regeneration with CO₂ recovered the catalyst reactivity.     

N-Positive ion activated rapid addition and mitochondrial targeting ratiometric fluorescent probes for in vivo cell H2S imaging

Heterocyclic compound quinoline and its derivatives exist in natural compounds and have a broad spectrum of biological activity.They play an important role in the design of new structural entities for medical applications.Similarly,indoles and their derivatives are found widely in nature.Amino acids,alkaloids and auxin are all derivatives of indoles,as are dyes,and their condensation with aldehydes makes it easy to construct reaction sites for nucleophilic addition agents.In this work,we combine these two groups organically to construct a rapid response site(within 30 s)for H₂S,and at the same time,a ratiometric fluorescence response is presented throughout the process of H₂S detection.As such,the lower detection limit can reach 55.7 nmol/L for H₂S.In addition,cell imaging shows that this probe can be used for the mitochondrial targeted detection of endogenous and exogenous H₂S.Finally,this probe application was verified by imaging H₂S in nude mice.     

A ternary mechanism for the facilitated transfer of metal ions onto metal–organic frameworks: implications for the ‘‘versatility’’ of these materials as solid sorbents

Although metal–organic frameworks offer a new platform for developing versatile sorption materials, yet coordinating the functionality, structure and component of these materials remains a great challenge. It depends on a comprehensive knowledge of a “real sorption mechanism”. Herein, a ternary mechanism for U(VI) uptake in metal–organic frameworks was reported. Analogous MIL-100s (Al, Fe, Cr) were prepared and studied for their ability to sequestrate U(VI) from aqueous solutions. As a result, MIL-100(Al) performed the best among the tested materials, and MIL-100(Cr) performed the worst. The nuclear magnetic resonance technique combined with energy-dispersive X-ray spectroscopy and zeta potential measurement reveal that U(VI) uptake in the three metal–organic frameworks involves different mechanisms. Specifically, hydrated uranyl ions form outer-sphere complexes in the surface of MIL-100s (Al, Fe) by exchanging with hydrogen ions of terminal hydroxyl groups (Al-OH₂, Fe-OH₂), and/or, hydrated uranyl ions are bound directly to Al(III) center in MIL-100(Al) through a strong inner-sphere coordination. For MIL-100(Cr), however, the U(VI) uptake is attributed to electrostatic attraction. Besides, the sorption mechanism is also pH and ionic strength dependent. The present study suggests that changing metal center of metal–organic frameworks and sorption conditions alters sorption mechanism, which helps to construct effective metal–organic frameworks-based sorbents for water purification.