妍媸·真鉴·慕道——论《聊斋志异》中的“化貌”篇章

《聊斋志异》中涉及人物面容妍媸变幻的小说约为八篇。这些篇章中人物"化貌"的实质是企图实现对苦难人生的逃逸和对无情时空的超越,其间寄托着作者对"真鉴"、对天下知音的热切渴求。而假象与真鉴、世道与自我、皮相与灵魂等富有哲理意味的问题,也在故事中得到了深入探讨。《聊斋》"化貌"篇章描摹了关爱苍生且情思细腻、风格飘洒的仙人形象,这种慕道的深层心理乃是作者对自由、广阔的精神家园的追寻。

Effect of Different Morphologies Induced by Solvent on ZIF-67 Derived Co@NC for Catalytic Phenol Hydrogenation

The Co@NC catalysts with different morphologies were prepared by two step process,solvent control growth and pyrolysis method.The polyhedral Co@NC-67P-450 catalyst has a relatively high CoNx content and exhibits excellent phenol hydrogenation activity(conversion 96.9%)at 160℃,3 MPa,which is higher than that of leaf shaped Co@NC-67L-450 catalyst(conversion 75.4%).We demonstrated Co_(3)O_(4)was reduced to the Co^(0)during the reaction.Moreover,CoNx species contribute to the superior hydrogenation activity of phenol.The Co-based catalysts can be easily recovered through the magnetic separation and performed the high stability.

Progresses and future directions on yardangs

Background,aim,and scope Yardang is a kind of typical wind-eroded landform in arid zones both on Earth and other planets.Their geomorphic process records the surface changes and climate,which may play a vital role in exploring the coupled landform-atmosphere system in arid zones.Recently,significant progresses have been made in this research field,and a review is still absent,which is the aim of the paper.Materials and methods Previous studies on the distribution,composition,morphology,and climatic driving force of yardang landform were reviewed.Results Earth yardang’s three evolutionary models were generalized:morphology evolution model,altitude evolution model and climate driven evolution model.Extraterrestrial yardang and its evolution are also summarized:the morphology is dominated by long ridges on Venus and Titan,and three yardang evolution hypotheses and an indirect dating method based on stratigraphic contact have been studied on Mars.Discussion In this study,firstly,the definition and morphology of yardang were described to define its characteristics.Secondly,we argue that yardang evolution has two dimensions:short-term variation and longterm variation.In the short-term variation,the morphological evolution of yardang on earth can be divided into four stages:embryonic stage,juvenile stage,mature stage,and demise stage.In the long-term variation,the evolution of yardang on earth is climate-driven,i.e.,it is controlled by atmospheric circulation changes during glacial-interglacial periods.Thirdly,yardang research on extraterrestrial bodies was also summarized:yardang has been found on Mars,Venus,and Titan,and the research focus by far are on geomorphology only.Conclusions(1)Yardang landform is an erosion landform with alternating ridges and troughs,with main form of whale back shape and fluctuations in the range of aspect ratios;(2)the short-term variation of yardang is manifested in its morphological evolution and height change,while the long-term variation is climate-driven;(3)based on Earth yardang,extraterrestrial yardang research has been carried out on Mars,Venus,and Titan.Recommendations and perspectives We then proposed that:(1)yardang formation ages,due to the erosion characteristics,are difficult to constraint;(2)the wind erosion capacity in the yardang areas might have been severely underestimated,making it essential to re-evaluate the previous paleoclimate reconstruction in the closed basins with limited chronological data;(3)yardang evolution is driven by climate change,but the coupling relationship between the yardang geomorphy and the air circulation is still unclear.Finally,future research directions:(1)more chronological data are needed,as well as the wind erosion capacity for yardang initiation and development;(2)the co-evolution of mid-low latitude landforms involved in yardang long-term variation and its relationship with global atmospheric circulation.

The effect of the carbon components on the performance of carbonbased transition metal electrocatalysts for the hydrogen evolution reaction

The hydrogen evolution reaction(HER)is a promising way to produce hydrogen,and the use of non-precious metals with an excellent electrochemical performance is vital for this.Carbon-based transition metal catalysts have high activity and stability,which are important in reducing the cost of hydrogen production and promoting the development of the hydrogen production industry.However,there is a lack of discussion regarding the effect of carbon components on the performance of these electrocatalysts.This review of the literature discusses the choice of the carbon components in these catalysts and their impact on catalytic performance,including electronic structure control by heteroatom doping,morphology adjustment,and the influence of self-supporting materials.It not only analyzes the progress in HER,but also provides guidance for synthesizing high-performance carbon-based transition metal catalysts.

Preparation and characterization of Ce-silane-ZrO_2 composite coatings on 1060 aluminum

In order to improve the property of traditional Ce-based conversion coatings, Ce-silane-ZrO2 composite coatings were successfully prepared on 1060 aluminum. The microstructure, chemical element composition and corrosion resistance of Ce-based conversion coatings and Ce-silane-ZrO2 composite coatings were investigated by SEM, AFM, XPS and EIS analyses. Stacking structure of the composite coating can be observed. The inner layer of the composite coatings mainly consists of oxide and hydroxide of Ce（Ⅲ）, and the silane network is composed of the outer layer together with a small amount of Ce（Ⅳ） hydroxide. By adding silane and ZrO2 nanoparticles into Ce-based conversion coatings, the porosity and the micro cracks of the coatings decrease apparently accompanying with the improvement of the corrosion resistance.

Effect of carbon addition on carbide morphology of single crystal Ni-based superalloy

Single crystal superalloys of AM3 with different carbon levels were prepared at withdraw rate of 50μm/s. The effect of carbon addition on the carbide morphology was investigated. It was found that there were four types of MC-type carbides, acicular, nodular, blocky, and Chinese script-type in the crystals. With an increase in carbon level, the volume fraction of carbide increased significantly while the volume fraction of eutectic decreased significantly. Furthermore, the size of carbide in high level carbon alloy became much larger.

Phase transitions, micro-morphology and its oxidation mechanism in oxidation of ilmenite (FeTiO_3) powder

Phase transitions, morphology changes, and oxidation mechanism of the ilmenite oxidation process were investigated. FeTi03 transforms to hematite and rutile when oxidation at 700-800 ℃, and pseudobrookite is formed when the oxidation temperature reaches 900 ℃. The initial ilmenite powder exhibits paramagnetism; however, after being oxidized at the intermediate temperature （800-850 ℃）, the oxidation product exhibits weak ferromagnetism. The oxidation mechanism was discussed. The microstructure observations show that a lot of micro-pores emerge on the surfaces of ilmenite particles at the intermediate temperature, which is deemed to be caoable ofenhancin~ the mass transfer ofoxgen during oxidation.

Comparative study on corrosion behavior of as-cast and extruded Mg-5Y-7Gd-1Nd-0.5Zr alloy in 5% NaCl aqueous solution

The corrosion behaviours of Mg-5Y-7Gd-1Nd-0.5Zr magnesium alloys prepared by as-casting and extrusion were investigated in 5% NaCl aqueous solution by immersion and electrochemical tests. The microstructure indicates the mean grain size of 15 μm for the extruded and 100 μm for the as-cast Mg-5Y-7Gd-1Nd-0.5Zr magnesium alloys. The corrosion morphology of as-cast sample shows pitting corrosion and little filiform corrosion, but that of the extruded sample shows pitting corrosion at the initial stage. The corrosion rate of extruded sample is higher than that of as-cast Mg-5Y-7Gd-1Nd-0.5Zr alloy according to the immersion test. The second phases containing RE acting as cathodes improve the corrosion properties. The corrosion potentials of as-cast and extruded Mg-5Y-7Gd-1Nd-0.5Zr alloys are -1.658 V and -1.591 V, respectively. The origins of the distinctive corrosion behavior of as-cast and extruded Mg-5Y-7Gd-1Nd-0.5Zr Mg alloys were discussed.

New Color-Difference Formula Based on CIECAM97s

To deduce a new color difference formula based on CIE 1997 Color Appearance Model(CIECAM97s), a color space J a 1 b 1 is first constructed with color appearance descriptors J,a,b in CIECAM97s. The new formula is then deduced in the space and named CDF CIECAM97s. The factors for lightness, chroma and hue correction in the formula are derived by linear regression according to BFD? CP data sets. It is found by statistical analysis that CDF CIECAM97s is in closer accordance with the visual assessments when compared with CMC(1∶1), CIE94 and CIE L *a *b * color difference formulae. Based on color appearance model, the new color difference formula can be used to predict color difference perception in a varity of different viewing conditions.

Morphology, photoluminescence and gas sensing of Ce-doped ZnO microspheres

Ce-doped ZnO microspheres were solvothermally prepared, and their microstructure, morphology, photoluminescence, and gas sensing were investigated by X-ray diffractometer, field emission scanning electron microscopy, transmission electron microscopy, fluorescence spectrometer and gas sensing analysis system. The results showed that the Ce-doped ZnO microspheres were composed of numerous nanorods with a diameter of 70 nm and a wurtzite structure. Ce-doping could cause a morphological transition from loose nanorods assembly to a tightly assembly in the microspheres. Compared with pure ZnO, the photoluminescence of the Ce-doped microspheres showed red-shifted UV emission and an enhanced blue emission. Particularly, the Ce-doped ZnO sensors exhibited much higher sensitivity and selectivity to ethanol than that of pure ZnO sensor at 320 °C. The ZnO microspheres doped with 6% Ce (mole fraction) exhibited the highest sensitivity (about 30) with rapid response (2 s) and recovery time (16 s) to 50×10?6 ethanol gas.

Oxidation roasting of molybdenite concentrate

In order to investigate the oxidation roasting of molybdenite concentrate in pure oxygen atmosphere, experiments at 673, 723, 773, 873 and 973 K were carried out. The phase transitions and morphology evolutions of the samples obtained at different temperatures after reacting for different time were analyzed by X-ray diffraction（XRD） and scanning electron microscopy（SEM）. The results showed that molybdenite concentrate was oxidized directly to Mo O3 in pure oxygen atmosphere. There were remarkable changes of the morphologies of products with the increase of the roasting temperature. It was also found that sintering phenomenon occurred during the roasting process in pure oxygen when the temperature was above 873 K. The composition of sintered sample was mainly comprised of Mo O3 and some unreacted Mo S2.

Effect of current frequency on properties of coating formed by microarc oxidation on AZ91D magnesium alloy

The microarc oxidation（MAO） coatings produced at different current frequencies on AZ91 D magnesium alloys were studied systematically. The morphologies, thickness, corrosion performances, and tribological properties of the coatings were investigated by the scanning electron microscopy, the electrochemical measurement system, and MS-T3000 friction test rig, respectively. The results show that the structure of the coatings becomes denser, and thickness becomes thinner with the increase of the current frequency. It is also found that the corrosion resistance of the coatings produced at higher frequency is improved greatly and the difference of the corrosion current density becomes small with increasing current frequency, which is similar to that of the coating thickness. The tribological test shows that the friction coefficient decreases with increasing the current frequency and the wear resistance of the coatings is influenced by both the thickness and structures. All these results were explained by analyzing the growing process of the MAO coating.

Variation of the second-phase morphology and its influence on fracture behavior of Al-Si alloy

Using an optical microscope and scanning electron microscope (SEM), the variation of eutectic Si morphology of Al-Si alloy in solution treatment was observed to study its influence on mechanical properties and fracture behavior. The results show that eutectic Si undergoes stubbing, necking, fragmentation, and growth in the initial stage (250 min); in the middle solution stage (250 to 400 min), the eutectic Si morphology has no significant change, only the degree of spheroidizing becomes higher; after 600 min, the growth of eutectic Si is a coarsening process controlled by diffusion and follows the Liftshitz-Slyozov-Wangner (LSW) model, and the eutectic Si morphology deteriorates due to the occurrence of facets and lap. Based on the quantitative measure and regression analysis, the eutectic Si morphology has a remarkable influence on mechanical properties and fracture behavior.

Low temperature solid-phase sintering of sintered metal fibrous media with high specific surface area

A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting process were first plated with a coarse copper coating layer by electroless plating process.A low-temperature sintering process was then completed at about 800 °C for 1 h under the protection of hydrogen atmosphere.The results show that a novel SMFM with complex surface morphology and high specific surface area（0.2 m2/g） can be obtained in this way.The effect of sintering temperature on the surface morphology and specific surface area of SMFM was studied by means of scanning electron microscopy and Brunauer-Emmett-Teller.The damage of micro-structure during the sintering process mainly contributed to the loss of specific surface area of SMFM and the optimal sintering temperature was 800 °C.

Microbially induced deposition of barium phosphates and its ingredient,morphology and size under different pH values

A phosphate-mineralization microbe was used to induce barium phosphates precipitation, and the precipitates with different types were obtained under different pH values. The average crystallite size of the barium phosphates was calculated by particle size distribution curves, and the size of the products was 33.40, 29. 37, 24. 13, 47.76 and 96. 53 μm when the pH values of the mixed solution are 7, 8, 9, 10 and 11, respectively. The results of X-ray diffraction （XRD） show that the structures of the particles controlled by the mixed solution are mainly BaaPO4 when pH 〈 10; the barium phosphates are synthesized by biological deposition which is the mixture of BaHPO4 and Ba5 （PO4）3OH when pH = 10; when pH = 11, the barium phosphates are also the mixtures, which are Ba5 （PO4）3OH and BaNaPO4. The above results indicate that the phosphate-mineralization microbe can produce a certain enzyme which constantly hydrolyzes phosphate monoester in the mixed solution, and then PO4^3- ions are obtained.

Research progress of Ag_3PO_4-based photocatalyst: Fundamentals and performance enhancement

Ag3PO4 is found to be a highly efficient photocatalyst and receives great attention. The high activity of the photocatalyst is credited to the intrinsic electronic structure. The morphology control and nano-composite fabrication are used to improve the performance and practicability. This paper reviews the structure, properties and some theoretical aspects of Ag3PO4 single crystal. Also, the major strategies, namely the morphology control and hetero-nanostructure construction, as ways to improve the performance of Ag3PO4-based photocatalysts, are summarized with the aid of some typical instances.

Surfactant-assisted hydrothermally synthesized MoS_2 samples with controllable morphologies and structures for anthracene hydrogenation

MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants（PEG,PVP,P123,SDS,AOT,and CTAB）on the morphologies and structures of MoS_2 samples were investigated.The results revealed that spherical,bulk-like,and flower-like MoS_2 particles assembled by NH4~＋-intercalated MoS_2 nano-sheets were synthesized.The morphologies of the MoS_2 samples and their structures（including the slab length and the number of stacked layers） of MoS_2 nano-sheets in these samples could be controlled by adjusting the surfactants.Mono-dispersed spherical MoS_2 particles could be synthesized with PEG via the creation of MoS_2 nano-sheets with slab lengths shorter than 15 nm and fewer than six stacked layers.Possible formation mechanisms of these MoS_2 samples created via surfactant-assisted hydrothermal processes are proposed.Further,the catalytic activities of MoS_2 samples for anthracene hydrogenation were evaluated in a slurry-bed reactor.The catalyst synthesized with the surfactant PEG exhibited the highest catalytic hydrogenation activity.Compared with the other catalysts,it had a smaller particle size,mono-dispersed spherical morphology,shorter slab length,and fewer stacked layers;these were all beneficial to exposing its active edges.This work provides an efficient approach to synthesize transition metal sulfides with controllable morphologies and structures.

Effects of Co_3O_4 nanocatalyst morphology on CO oxidation:Synthesis process map and catalytic activity

This study focuses on drawing a hydrothermal synthesis process map for Co3O4 nanoparticles with various morphologies and investigating the effects of Co3O4 nanocatalyst morphology on CO oxidation.A series of cobalt-hydroxide-carbonate nanoparticles with various morphologies（i.e.,nanorods,nanosheets,and nanocubes） were successfully synthesized,and Co3O4 nanoparticles were obtained by thermal decomposition of the cobalt-hydroxide-carbonate precursors.The results suggest that the cobalt source is a key factor for controlling the morphology of cobalt-hydroxide-carbonate at relatively low hydrothermal temperatures（≤ 140℃）.Nanorods can be synthesized in CoCl2 solution,while Co（NO3）2 solution promotes the formation of nanosheets.Further increasing the synthesis temperature（higher than 140 ℃） results in the formation of nanocubes in either Co（NO3）2 or CoCl2 solution.The reaction time only affects the size of the obtained nanoparticles.The presence of CTAB could improve the uniformity and dispersion of particles.Co3O4 nanosheets showed much higher catalytic activity for CO oxidation than nanorods and nanocubes because it has more abundant Co^（3＋） on the surface,much higher reducibility,and better oxygen desorption capacity.

Recent advances on Bi_(2)WO_(6)‐based photocatalysts for environmental and energy applications

Bismuth tungstate(Bi_(2)WO_(6))has become a research hotspot due to its potential in photocatalytic energy conversion and environmental purification.Nevertheless,the limited light absorption and fast recombination of photogenerated carriers hinder the further improvement of the photocatalytic performance of Bi_(2)WO_(6).Herein,we provide a systematic review for the recent advances on Bi_(2)WO_(6)‐based photocatalysts.It starts with the crystal structure,optical properties and photocatalytic fundamentals of Bi_(2)WO_(6).Then,we focus on the modification strategies of Bi_(2)WO_(6)based on morphology control,atomic modulation and composite fabrication for diverse photocatalytic applications,such as organic synthesis,water splitting,CO2 reduction,water treatment,air purification,bacterial inactivation,etc.Finally,some current challenges and future development prospects are proposed.We expect that this review can provide a useful reference and guidance for the development of efficient Bi_(2)WO_(6)photocatalysts.

Electronic and geometric structure of the copper-ceria interface on Cu/CeO2 catalysts

The atomic structure of the active sites in Cu/CeO2 catalysts is intimately associated with the copper-ceria interaction. Both the shape of ceria and the loading of copper affect the chemical bonding of copper species on ceria surfaces and the electronic and geometric character of the relevant interfaces. Nanostructured ceria, including particles(polyhedra), rods, and cubes, provides anchoring sites for the copper species. The atomic arrangements and chemical properties of the(111),(110) and(100) facets, preferentially exposed depending on the shape of ceria, govern the copper-ceria interactions and in turn determine their catalytic properties. Also, the metal loading significantly influences the dispersion of copper species on ceria with a specific shape, forming copper layers, clusters, and nanoparticles. Lower copper contents result in copper monolayers and/or bilayers while higher copper loadings lead to multi-layered clusters and faceted particles. The active sites are usually generated via interactions between the copper atoms in the metal species and the oxygen vacancies on ceria, which is closely linked to the number and density of surface oxygen vacancies dominated by the shape of ceria.