采棉机机架体静力分析研究

基于ANSYS Workbench对采棉机机架体进行有限元分析,把机架体上装配零件经过适当简化处理加载到机架板上,得出机架上板和中间板为承受应力较大的零件。经强度校核,机架强度满足正常工作要求。

2100BL电铲上机架体的修复设计

2100BL型电铲是美国P&H采矿设备公司研制的大型矿用机械式正铲挖掘机,因工况条件恶劣,负载变化很大,受冲击载荷频率高,其零部件极易受损。从结构上来说,上机架体是主要受力机构,也是最易受损的结构件之一,在工作中受力最大,必须同时具有抗压、抗弯、抗扭等特性。本文主要介绍了如何应用焊接和精加工技术来修复电铲上机架体的工艺。

浅谈无机房电梯机架体结构设计

无机房电梯井道结构各异,本文通过对设计过程碰到的非标结构进行分析,从而得出了一些设计解决方案。

巨型水轮发电机下机架工地制造翻身工艺研究

某巨型水轮发电机下机架中心体须在工地现场进行生产制造。为满足焊接、质检等工序操作要求,在制造过程中必须进行翻身,巨型水轮发电机下机架中心体在工地制造过程中翻身尚属首次,无可借鉴的经验,本文通过对工地现场条件分析,制定了下机架中心体翻身工艺,解决了下机架中心体工地现场翻身难题,该翻身工艺在安全性、可靠性、翻身效率方面都优于常规的翻身工艺。

Strategies for engineering metal-organic frameworks as efficient photocatalysts

Environmental pollution and energy deficiency represent major problems for the sustainability of the modern world. Photocatalysis has recently emerged as an effective and environmentally friendly technique to address some of these sustainability issues,although the key to the success of this approach is dependent on the photocatalysts themselves. Based on their attractive physic chemical properties,including their ultrahigh surface areas,homogeneous active sites and tunable functionality,metal-organic frameworks（MOFs） have become interesting platforms for the development of solar energy conversion devices. Furthermore,MOFs have recently been used in a wide variety of applications,including heterogeneous photocatalysis for pollutant degradation,organic transformations,hydrogen production and CO2 reduction. In this review,we have highlighted recent progress towards the application of MOFs in all of these areas. We have collected numerous reported examples of the use of MOFs in these areas,as well as providing some analysis of the key factors influencing the efficiency of these systems. Moreover,we have provided a detailed discussion of new strategies that have been developed for enhancing the photocatalytic activity of MOFs. Finally,we have provided an outlook for this area in terms of the future challenges and potential prospects for MOFs in photocatalysis.

Amine-grafted on lanthanide metal-organic frameworks:Three solid base catalysts for Knoevenagel condensation reaction

A post-synthetic modification strategy has been used to prepare three solid base catalysts, including Er（btc）（ED）075（H2O）0.25 （2, btc = 1,3,5-benzenetricarboxylates, ED = 1,2-ethanediamine）, Er（btc）（PP）0.55（H20）0.45 （3, PP = piperazine）, and Er（btc）（DABCO）0.15（H2O）0.85 （4, DABCO = 1,4- diazabicyclo[2.2.2]octane）, by grafting three different diamines onto the coordinatively unsaturated Er（III） ions into the channels of the desolvated lanthanide metal-organic framework （Er（otc））. The resulting metal-organic frameworks were characterized by elemental analysis, thermogravimetric analysis, powder X-ray diffraction, and N2 adsorption. Based on its higher loading ratio of the diamine, as well as its greater stability and porosity, catalyst 2 exhibited higher catalytic activity and reusability than catalysts 3 and 4- for the Knoevenagel condensation reaction. The catalytic mechanism of 2 has also been investigated using size-selective catalysis tests.

3D-ordered macroporous N-doped carbon encapsulating Fe-N alloy derived from a single-source metal-organic framework for superior oxygen reduction reaction

Fe-N compounds with excellent electrocatalytic oxygen reduction activity are considered to be one of the most promising non-precious metal materials for fuel cells.Fe-N compounds with excellent electrocatalytic oxygen reduction activity are considered to be one of the most promising non-precious metal materials for fuel cells,which focuses on the Fe-N4 single-atom catalysts and the iron nitride materials(such as Fe2N and Fe3N).A hybridized catalyst having a hierarchical porous structure with regular macropores could enable the desired mass transfer efficiency in the catalytic process.In this study,we have constructed a new type of hybrid catalyst having iron and iron-nitrogen alloy nanoparticles(Fe-N austenite,termed as Fe-NA)embedded in the three-dimensional ordered macroporous N-doped carbon(3DOM Fe/Fe-NA@NC)by direct pyrolysis of single-source dicyandiamide-based iron metal-organic frameworks.The as-synthesized composites preserve the hierarchical porous carbon framework with ordered macropores and high specific surface area,incorporating the uniformly dispersed iron/iron-nitrogen austenite nanoparticles.Thereby,the striking architectural configuration embedded with highly active catalytic species delivers a superior oxygen reduction activity with a half-wave potential of 0.88 V and a subsequent superior Zn-air battery performance with high open-circuit voltage and continuous stability as compared to those using a commercial 20%Pt/C catalyst.

Structure and denitration performance of carbon-based catalysts prepared from Cu-BTC precursor

Using Cu-BTC prepared by hydrothermal method as precursor, carbon-based catalysts were obtained as model materials for low-temperature DeNO_x. These catalysts were characterized by X-ray diffractometry（XRD）, Raman spectroscopy, scanning electron microscopy（SEM） and energy dispersive X-ray spectrometry（EDS）. The results showed that all carbon-based catalysts held the octahedron shape of Cu-BTC in most parts, and they mainly consisted of face-centered cubic copper. CuO_x/C exhibited excellent catalytic activity, and such catalytic activity was further improved with the introduction of Ag. The catalyst with a Cu to Ag mole ratio of 6：1 and an activated temperature of 600 °C showed the best catalytic performance, and its catalytic denitration rate reached 100% at a temperature as low as 235 °C. During the catalytic reaction process, Cu~＋ mainly played a catalytic role.

Covalent organic frameworks as heterogeneous catalysts

Covalent organic frameworks （COFs）, established as an emerging class of crystalline porous polymers with high surface area, structural diversity, and esignability, attract much interest and exhibit potential applications in catalysis. In this review, we summarize the use of COFs as a versatile platform to develop heterogeneous catalysts for a variety of chemical reactions. Catalytic COFs are categorized in accordance with the types of active sites, involving single functional active sites, bifunctional active sites, and metal nanoparticles （NPs） embedded in pores. Special emphasis is placed on the deliberate or incidental synthesis strategies, the stability, the heterogeneity, and the shape/size selectivity for COF catalysis. Moreover, a description of the application of COFs as photocatalysts and electrocatalysts is presented. Finally, the prospects of COFs in catalysis and remaining issues in this field are indicated.

Dimension-Controllable and Photo-Responsive Supramolecular Organic Framworks through Cucurbit[8]uril-based Self-Assembly

Dimension-controllable supramolecular organic frameworks(SOFs)with aggregation-enhanced fluorescence are hierarchically fabricated through the host-guest interactions of cucurbit[8]uril(CB[8])and coumarin-modified tetraphenylethylene derivatives(TPEC).The three-dimensional layered SOFs could be constructed from the further stacking of two-dimensional mono-layered structures via simply regulating the self-assembly conditions including the culturing time and concentration.Upon light irradiation under the wavelength of 365 nm,the photodimerization of coumarin moieties occurred,which resulted in the transformation of the resultant TPECn/CB[8]4n two-dimensional SOFs into robust covalently-connected 2D polymers with molecular thickness.Interestingly,the supramolecular system of TPEC/CB[8]exhibited intriguing multicolor fluorescence emission from yellow to blue in the time range of 0-24 h at 365 nm irradiation,possessing potential applicability for photochromic fluorescence ink.

Development of a bismuth-based metal-organic framework for photocatalytic hydrogen production

A novel 3 D bismuth-organic framework(called Bi-TBAPy) single crystal was synthesized by employing 1,3,6,8-tetrakis(p-benzoic acid)pyrene(H4TBAPy) as an organic linker. The study demonstrates that the Bi-TBAPy not only possesses good chemical stability and suitable band edge positions for promising photocatalytic H2 evolution, but it also exhibits a typical ligand-to-metal charge transfer for favorable charge separation. The photocatalytic H2 evolution rates on the as-obtained Bi-TBAPy with different cocatalysts modified were examined with triethanolamine as the sacrificial reagent. Based on this, the hydrogen evolution rate of 140 μmol h-1 g-1 was obtained on the optimized sample with a loading of 2 wt% Pt as a cocatalyst. To the best of our knowledge, this is the first bismuth-based metal-organic framework(MOF) that functions as an effective photocatalyst for photocatalytic water reduction. Our study not only adds a new member to the family of photocatalyst materials, but also reveals the importance of cocatalyst modification in improving photocatalytic activity of MOFs.

Direct and Indirect Excitons in Two-Dimensional Covalent Organic Frameworks

Highly luminescent bulk two-dimensional covalent organic frameworks(COFs)attract much attention recently.Origin of their luminescence and their large Stokes shift is an open question.After first-principles calculations on two kinds of COFs using the GW method and Bethe-Salpeter equation,we find that monolayer COF has a direct band gap,while bulk COF is an indirect band-gap material.The calculated optical gap and optical absorption spectrum for the direct excitons of bulk COF agree with the experiment.However,the calculated energy of the indirect exciton,in which the photoelectron and the hole locate at the conduction band minimum and the valence band maximum of bulk COF respectively,is too low compared to the fluorescence spectrum in experiment.This may exclude the possible assistance of phonons in the luminescence of bulk COF.Luminescence of bulk COF might result from exciton recombination at the defects sites.The indirect band-gap character of bulk COF originates from its AA-stacked conformation.If the conformation is changed to the AB-stacked one,the band gap of COF becomes direct which may enhance the luminescence.

A Comparative Analysis of China ICT Regulation Effectiveness Based on an IEP Framework

In order to conduct a comparative analysis on China's Telecommunications/ICT regulation effectiveness to make up the omission of international researches,and to find out the difference between China and other countries and try to improve China's ICT regulation effectiveness,this paper developed an extended,integrated ICT regulation effectiveness assessment framework,with a name of IEP framework that consists of three assessment directions,namely regulation institution,regulation enforcement and industry performance.Based on this framework and by using Entropy Method,the paper then selected 10 sample countries,including China,six developed countries,and other three developing countries,and made a comprehensive comparison evaluation for those countries.Finally,by focusing on China's results of ranking 10 in institution,6 in enforcement,5 in performance and 8 in total ranking,the paper gave the explanation and presented improvement suggestions for the future ICT regulation in China.

Metal organic framework‐ionic liquid hybrid catalysts for the selective electrochemical reduction of CO_(2) to CH4

The electrochemical reduction of CO_(2) towards hydrocarbons is a promising technology that can utilize CO_(2) and prevent its atmospheric accumulation while simultaneously storing renewable en‐ergy.However,current CO_(2) electrolyzers remain impractical on a large scale due to the low current densities and faradaic efficiencies(FE)on various electrocatalysts.In this study,hybrid HKUST‐1 metal‐organic framework‒fluorinated imidazolium‐based room temperature ionic liquid(RTIL)electrocatalysts are designed to selectively reduce CO_(2) to CH_(4).An impressive FE of 65.5%towards CH_(4) at-1.13 V is achieved for the HKUST‐1/[BMIM][PF_(6)]hybrid,with a stable FE greater than 50%maintained for at least 9 h in an H‐cell.The observed improvements are attributed to the increased local CO_(2) concentration and the improved CO_(2)‐to‐CH_(4) thermodynamics in the presence of the RTIL molecules adsorbed on the HKUST‐1‐derived Cu clusters.These findings offer a novel approach of immobilizing RTIL co‐catalysts within porous frameworks for CO_(2) electroreduction applications.

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.

In situ doping brushite on zinc manganese oxide toward enhanced water oxidation performance: Mimicry of an oxygen‐evolving complex

We report in situ doping of brushite on zinc manganese oxide（ZMO）, fabricated by calcining a Mn（II） oxalate‐impregnated metal‐organic framework. The doping process was conducted in com‐bination with the photocatalytic water oxidation reaction which was catalyzed by ZMO in neutral phosphate‐buffered aqueous solution containing [Ru（bpy）3]^2＋‐Na2S2O8 and calcium（II） triflate salt, exhibiting greatly enhanced water oxidation performance with optimized turnover frequency of 0.18 mmol（O2） mol（Mn）^（–1） s^（–1）. Different analytical techniques indicated that photodeposited calci‐um‐phosphate（CaP） acted as a co‐catalyst to promote the O2 evolution activity of ZMO. This system involved the use of manganese oxide and calcium ion, and the operation was conducted under am‐bient temperature and neutral conditions, thus, it efficiently mimicked the oxygen‐evolving complex in photosystem II.

Metal‐organic framework‐derived multifunctional photocatalysts

Metal‐organic framework(MOF)‐derived nanomaterials have attracted widespread attention,because the excellent features,such as high surface area,porosity and tunable properties are inherited from MOFs.Moreover,the derivatives avoid the poor conductivity and stability of MOFs.MOF‐derived nanomaterials can easily be regulated by a specific selection of metal nodes and organic linkers,resulting in multifunctionality in photocatalysis.MOF derivatives can be used not only as semiconductor photocatalysts,but also as co‐catalysts for photocatalytic hydrogen evolution,CO_(2) reduction,pollutants degradation,etc.This review focuses on the multifunctional applications of MOF derivatives in the field of photocatalysis.The researches in recent years are analyzed and summarized from the aspects of preparation,modification and application of MOF derivatives.At the end of the review,the development and challenges of MOF derivatives applied in photocatalysis in the future are put forward,in order to provide more references for further research in this field and bring new inspiration.

Substitution for In Vitro and In Vivo Tests:Computational Models from Cell Attachment to Tissue Regeneration

To get an optimal product of orthopaedic implant or regenerative medicine needs to follow trialand-error analyses to investigate suitable product’s material,structure,mechanical properites etc.The whole process from in vivo tests to clinical trials is expensive and time-consuming.Computational model is seen as a useful analysis tool to make the product development.A series of models for simulating tissue engineering process from cell attachment to tissue regeneration are reviewed.The challenging is that models for simulating tissue engineering processes are developed separately.From cell to tissue regeneration,it would go through blood injection after moving out the defect;to cell disperse and attach on the scaffold;to proliferation,migration and differentiation;and to the final part-becoming mature tissues.This paper reviewed models that related to tissue engineering process,aiming to provide an opportunity for researchers to develop a mature model for whole tissue engineering process.This article focuses on the model analysis methods of cell adhesion,nutrient transport and cell proliferation,differentiation and migration in tissue engineering.In cell adhesion model,one of the most accurate method is to use discrete phase model to govern cell movement and use Stanton-Rutland model for simulating cell attachment.As for nutrient transport model,numerical model coupling with volume of fluid model and species transport model together is suitable for predicting nutrient transport process.For cell proliferation,differentiation and migration,finite element method with random-walk algorithm is one the most advanced way to simulate these processes.Most of the model analysis methods require further experiments to verify the accuracy and effectiveness.Due to the lack of technology to detect the rate of nutrient diffusion,there are especially few researches on model analysis methods in the area of blood coagulation.Therefore,there is still a lot of work to be done in the research of the whole process model method of tissue engineering.In the future,the numerical model would be seen as an optimal way to investigate tissue engineering products bioperformance and also enable to optimize the parameters and material types of the tissue engineering products.

Single crystal metal-organic framework constructed by vertically self-pillared nanosheets and its derivative for oriented lithium plating

This vertically self‐pillared(VSP)structure extends the application range of traditional porous materials with facile mass/ion transport and enhanced reaction kinetics.Here,we prepare a single crystal metal‐organic framework(MOF),employing the ZIF‐67 structure as a proof of concept,which is constructed by vertically self‐pillared nanosheets(VSP‐MOF).We further converted VSP‐MOF into VSP‐cobalt sulfide(VSP‐CoS2)through a sulfidation process.Catalysis plays an important role in almost all battery technologies;for metallic batteries,lithium anodes exhibit a high theoretical specific capacity,low density,and low redox potential.However,during the half‐cell reaction(Li++e=Li),uncontrolled dendritic Li penetrates the separator and solid electrolyte interphase layer.When employed as a composite scaffold for lithium metal deposition,there are many advantage to using this framework:1)the VSP‐CoS2 substrate provides a high specific surface area to dissipate the ion flux and mass transfer and acts as a pre‐catalyst,2)the catalytic Co center favors the charge transfer process and preferentially binds the Li+with the enhanced electrical fields,and 3)the VSP structure guides the metallic propagation along the nanosheet 2D orientation without the protrusive dendrites.All these features enable the VSP structure in metallic batteries with encouraging performances.

Power Delivery Studies of Windbelt Generators with Different Architectures

Windbelt generators have been proposed as small, green power sources for battery charging applications. Some of the reported results lack detailed information about how key parameters influence the output power of the generator. In this work, we built prototypes with different architectures to study the voltage generation and power delivery as functions of belt tension, length, and electrical load at various wind speeds. We also studied the maximum power delivery conditions before the breakdown of the belt oscillation occurs. Our results are obtained from windbelt generators with two types of architectures： a conventional design with an adjustable belt that uses weight for tension control, and a revised design with a belt oscillation perpendicular to the coil axis. We have concluded that the breakdown of the belt oscillation at lower output resistances is a primary bottleneck that will limit windbelt systems to only very low power applications.