新疆诺尔特地区金、多金属成矿地球动力学背景

诺尔特地区位于北阿尔泰构造带的东部,西伯利亚板块西南缘。该区地球动力学背景的演化与北阿尔泰一致,其演化经历了基底陆壳、拉张型过渡壳、汇聚型过渡壳、新陆壳及新陆壳在中生代的发展等阶段。金、多金属成矿为燕山期南北挤压、构造活化动力学背景下的产物,与新陆壳在中生代的发展有关。

山东省海阳市招虎山岩体西南金、多金属成矿研究及找矿方向

招虎山岩体位于胶莱盆地的北缘胶东地区重要的成矿区带上,具较好成矿条件好。本文探讨了成矿作用及成矿规律,对金、多金属找矿方向进行了总结。

Manufacture, characterization and application of porous metal-fiber sintered felt used as mass-transfer-controlling medium for direct methanol fuel cells

Fabrication, characterization and performance of a porous metal-fiber sintered felt （PMFSF） based on multi-tooth cutting and solid-phase sintering were studied. The PMFSF was used as the anodic methanol barrier in a passive air-breathing direct methanol fuel cell to mitigate the effects of methanol crossover. Compared with the commercial SUS316L felt made of bundle-drawn fibers, this self-made PMFSF has larger pore diameter, polarized pore distribution, irregular fiber shape, rougher surface, lower mass flow resistance and evident hydrophobicity. The results reveal that the use of a PMFSF significantly enhances the cell performance since it helps to maintain a balance between the reactant and product management while depressing methanol crossover. The PMFSF with a porosity of 70% yields the highest cell performance at a methanol concentration of 4 mol/L.

Rock-forming mechanism of Qingshanjiao intrusion in Dongguashan copper(gold) deposit, Tongling area, Anhui province, China

Dongguashan deposit is a large porphyry-skarn copper（gold） deposit in Tongling ore district. The Qingshanjiao intermediate acid intrusion of Yanshanian had a direct genetic relationship with mineralization. The magma origin, rock-forming dynamic background and rock-forming process were studied, and the rock-forming mechanism of Qingshanjiao intrusion was discussed, based on geological characteristics, detailed observation of petrography and systematic investigation of petrochemistry, trace elements and REE geochemistry characteristics of Qingshanjiao intrusion. The results show that Qingshanjiao rock body belongs to high-K calc-alkaline series with higher LREE elements, Th, Rb and Sr abundance, but depleted in HREE elements, Ba, Nb and Ta. The primary magma originated from the mantle-crust mixtures which were caused by basaltic magma of mantle mixing with syenite magma of partial melting of the lower crust, and the formation environment of Qingshanjiao intrusion was emplaced in the transitional environment from compression to extension. The Harker diagram and hybrid structures of plagioclase and potassium feldspar indicate that the fractional crystallization occurred in the process of magmatic evolution. The petrochemistry, trace elements and REE geochemistry characteristics indicate that the magma was contaminated by crustal material during the rock-forming. These results suggested that the Qingshanjiao intrusion was formed by fractional crystallization and assimilation and hybridization of mantle-crust magma in the transitional environment from compression to extensional.

Solvothermal synthesis of Co-substituted phosphomolybdate acid encapsulated in the UiO-66 framework for catalytic application in olefin epoxidation

Hybrid composites of phosphomolybdic acid@UiO-66(PMo12@UiO-66)and Co-substituted phosphomolybdic acid@UiO-66(PMo11Co@UiO-66)were synthesized using the direct solvothermal method.A variety of characterization results demonstrated that phosphomolybdic acid(PMo12)or Co-substituted phosphomolybdate acid(PMo11Co)clusters are uniformly dispersed in the cages of Zr-based metal-organic UiO-66 frameworks.The catalytic properties of these hybrid composites were investigated by applying the epoxidation of olefins with tert-butyl hydroperoxide as the oxidant.Compared to PMo12@UiO-66,PMo11Co@UiO-66 showed a much higher catalytic activity and was simply recovered by filtration and reused for at least ten runs without significant loss of catalytic activity.Particularly,PMo11Co@UiO-66 can efficiently convert cyclic olefins like limonenes to epoxides,and its selectivity to 1,2-limonene oxide reached 91%in the presence of a radical inhibitor such as hydroquinone.The excellent catalytic activity and stability of the hybrid composite PMo11Co@UiO-66 are mainly attributed to the uniform distribution of highly active PMo11Co units within the smaller cages of UiO-66,to the suitable surface polarity of the hybrid composite for facilitating the access of reagents and solvent,and to the strong interface-interactions between the polyoxometalate and the UiO-66 framework.

Light alloying element‐regulated noble metal catalysts for energy‐related applications

Noble metals have been widely used as heterogeneous catalysts because they exhibit high activity and selectivity for many reactions of both academic and industrial interest.The introduction of light atomic species(e.g.,H,B,C,and N)into noble metal lattices plays an important role in optimizing catalytic performance by modulating structural and electronic properties.In this review,we present a general overview of the recent advances in the modification of noble metals with light alloying elements for various catalytic reactions,particularly for energy‐related applications.We summarize the types,location,concentration,and ordering degree of light atoms as major factors in the performance of noble metal‐based catalysts,with emphasis on how they can be rationally controlled to promote activity and selectivity.We then summarize the synthetic strategies developed to incorporate light elements and highlight the theoretical and experimental methods for understanding the alloying effects.We further focus on the wide usage of noble metal‐based catalysts modified with different light alloying atoms and attempt to correlate the structural features with their catalytic performances.Finally,we discuss current challenges and future perspectives regarding the development of highly efficient noble metal‐based catalysts modified with light elements.

Dissolution kinetics of copper from multi-metal copper alloy roasted in oxygen

A kinetic study on the sulfuric acid leaching of multi-metal oxide, which is the product of multi-metal copper alloy with iron trioxide roasted in oxygen, was carried out. The effects of leaching time, stirring speed, sulfuric acid concentration, reaction temperature, and particle size of the multi-metal oxide on the kinetics and mechanism of copper extraction were studied. It was found that the reaction kinetic model about the copper extraction from multi-metal oxide follows the mixed kinetic shrinking core mode： 1/31n（1-X）＋（1-X）-l/3-1=680.5C（H2SO4）0.4297dp0.75115exp（-Ea/RT）t.

Hot deformation behavior and related microstructure evolution in Au−Sn eutectic multilayers

Hot compression was performed on a multilayered Au−20Sn eutectic alloy to investigate the deformation behavior and microstructure evolution.During hot compression,microstructural spheroidization was initiated from plastic instability regions,and it was preferentially activated in vertical lamellae with a growth direction parallel to the compressive direction.Continuous dynamic recrystallization associated with lattice dislocations was the mechanism in both AuSn and Au5Sn multilayers.After spheroidization,strain accumulations were weakened in both of the equiaxed phases,and the deformation mechanism was substantially replaced by grain boundary sliding and migration.Based on these findings,hot rolling was conducted on an as-cast Au−20Sn alloy and a foil with a thickness of~50μm was successfully prepared.The present study can promote the development of Au−20Sn foils,and provide insights into the deformation behavior and microstructure evolution of multilayered eutectic alloys.

Research advances of light-driven hydrogen evolution using polyoxometalate-based catalysts

With the increasing concerns to energy shortage and environmental problems in modern society,the development of cheap,clean,and sustainable energy alternatives has been attracting tremendous attention globally.Among various strategies of renewable energy exploration,solar-driven water splitting into its compositional elements H2 and O2 is an ideal approach to convert and store renewable solar energy into chemical bonds.In recent few decades,as an emerging new type of catalysts,polyoxometalates(POMs)have been widely utilized for water splitting due to their versatile synthetic methodology and highly tunable physicochemical and photochemical properties.This critical review addresses the research advances of light-driven hydrogen evolution using polyoxometalate-based catalysts,including plenary POMs,transition-metal-substituted POMs,POM@MOF composites,and POM-semiconductor hybrids,under UV,near UV and visible light irradiation.In addition,the catalytic mechanism for each reaction system has been thoroughly discussed and summarized.Finally,a comprehensive outlook of this research area is also prospected.

Li_(x)Cu alloy nanowires nested in Ni foam for highly stable Li metal composite anode

Porous metal architectures are widely adopted as three-dimensional conducting scaffolds for constructing Li metal composite anodes,whereas their macropores hinder their practical application due to limited surface area and large pore size of few hundred micrometers.In this work,a network of Li_(x)Cu solid solution alloy nanowires is in situ formed via infiltrating molten Li-Cu alloy into Ni foam and subsequent cooling treatment,whereby a three-component composite anode consisting of Li metal,Li_(x)Cu alloy,and Ni foam is fabricated.The Li_(x)Cu nanowires nested as secondary frame split the macropores into micropores,enlarging the active surface area and inducing uniform Li deposition significantly.The lithiophilicity of the alloy wires and the shrunken void size built by the hierarchical architecture can further tune the nucleation and growth behavior of Li.The multiscale synergetic effect between the primary and secondary scaffold guarantees the composite anode sheet with extraordinarily long-term cycling stability even under high current rates.

Porous bimetallic Pt-Fe nanocatalysts for highly efficient hydrogenation of acetone

Porous Pt-Fe bimetallic nanocrystals have been synthesized via self-assembly and can effectively facilitate the synthesis of 2-propanol from acetone. The bimetallic catalyst has three--dimensional channels and shows turnover frequencies （TOFs） of up to 972 h^-1 for a continuous process more than 50 h. Preliminary mechanistic studies suggest that the high reactivity is related to the interface consisting of a bimetallic Pt-Fe alloy and Fe2O3-x. An understanding of real catalytic behavior and the catalytic mechanism based on model systems has been shown to help fabricate an improved Pt/Fe3O4 catalyst with increased activity and lifetime which has great potential for large-scale industrial applications.

Manufacture of porous metallic glass using dissolvable templates

A facile,precise,and controllable manufacturing technology is desired for hierarchical functional surfaces.In this work,we successfully manufactured porous metallic glass using a water-dissolution material as template and the excellent thermoplastic property of metallic glass.The prepared micro/nanostructures have excellent tunability,and the proposed approach can be used to prepare large-area disordered porous structures and ordered regular arrays with nanoscale replication accuracy.In particular,the disordered porous structure prepared by the dissolvable template strategy exhibits a water contact angle of~140°and an oil contact angle of~0°,making it suitable for oil/water separation.It also shows stable wettability after being soaked in strong acid or alkali environments and maintains a~130°water contact angle and a~4°oil contact angle even after severe wear.The proposed strategy also possesses excellent recycling properties.We reconstructed porous structures on the same surface three times and found no significant change in wettability for each reconstructed porous structure.Our research provides a facile and controllable approach for the preparation of hierarchical porous structures and paves the way for the design of other functional surfaces.

Localization and macroscopic instability in nanoporous metals

Ductile fracture generally relates to microscopic voiding and to strain localization in metallic materials.When the void size is reduced to the nanoscale,size effects often lead to a different macroscopic plastic behavior from that established for the same material with larger voids.For example,irradiation of metallic materials can generate a large number of voids at the nanoscale,leading to complex deformation behaviors.The present work advances the understanding of strain localization in nanoporous metallic materials,connecting both the microscopic(nano-)and macroscopic scales.To explore the physical mechanisms at the nanoscale,molecular dynamics(MD)simulations were here carried out,capturing multiple nanovoids explicitly.Then,a homogenized continuum theory based in Gurson's constitutive framework is proposed,which enables us to explore how localized behavior at the macroscopic scale evolves.The homogenized model incorporates the surface tension associated with nanosized void.The importance of this surface tension is illustrated by several parametric studies on the conditions of localization,when a specimen is subjected to uniaxial tension.Our parametric studies show that for smaller nanovoid sizes,and for a hardening matrix material,shear localization onset is delayed.Our proposed homogenization model was then used to predict localization behavior captured by our MD simulation.The yield stress and the localization strain predicted by our continuum model are in general agreement with the trends obtained by MD simulation.Moreover,based on our present study,experimental results of shear failure strain vs.dose of irradiation for several metals could be qualitatively explained rather successfully.Our model can therefore help shed light on prolonging the operation limits and the lifetime of irradiated metallic materials under complex loading conditions.

An oxidation-nitridation-denitridation approach to transform metal solids into foams with adjustable pore sizes for energy applications

Metal foams with hierarchically porous structures are highly desirable in energy applications as active materials or their host substrates.However,conventional preparation methods usually have a quite limited flexibility of adjusting pore size of metal foams.Herein,an alternative new method based on gaseous thermal oxidation-nitridation-denitridation processes was developed to prepare metal(copper and nickel)foams with adjustable pore size by controlling the thermal nitridation temperature.Moreover,this environment-friendly method is independent of the shape of starting pure metal substrates and can be repeatedly applied to the metal substrates to create hierarchical porous structures containing different size pores.As a demonstration of the advantages of the resultant foams with abundant pores by this method,compared with its starting material(commercial Ni foam with the pore size of several millimeters),the resultant hierarchical porous Ni foam gives the remarkably enhanced performance of electrochemical water splitting as HER/OER electrodes and electrochemical energy storage as the host substrate of capacitive material MnO2.The metal foams with adjustable pore size prepared by the developed method will find a wide range of important applications in energy storage and conversion areas.