Porous TiFe_(2) intermetallic compound fabricated via elemental powder reactive synthesis

Porous intermetallics show potential in the field of filtration and separation as well as in the field of catalysis.Herein,porous Ti Fe2intermetallics were fabricated by the reactive synthesis of elemental powders.The phase transformation and pore formation of porous TiFe2intermetallics were investigated,and its corrosion behavior and hydrogen evolution reaction(HER)performance in alkali solution were studied.Porous TiFe2intermetallics with porosity in the range of 34.4%-56.4%were synthesized by the diffusion reaction of Ti and Fe elements,and the pore formation of porous TiFe2intermetallic compound is the result of a combination of the bridging effect and the Kirkendall effect.The porous TiFe2samples exhibit better corrosion resistance compared with porous 316L stainless steel,which is related to the formation of uniform nanosheets on the surface that hinder further corrosion,and porous TiFe2electrode shows the overpotential of 220.6 and 295.6 mV at 10 and 100 mA·cm-2,suggesting a good catalytic performance.The synthesized porous Fe-based intermetallic has a controllable pore structure as well as excellent corrosion resistance,showing its potential in the field of filtration and separation.

A review on surface coating strategies for anti-hygroscopic of high energy oxidizer ammonium dinitramide

Ammonium dinitramide(ADN),which has the advantages of high energy density,no halogen and low characteristic signal,is not only considered as a new high-energy oxidizer that is expected to replace the traditional oxidizer ammonium perchlorate(AP)in solid propellants,but also a good performance explosive in itself.However,due to the strong hygroscopicity of ADN,its application in solid propellants and explosives is greatly limited.Solving the hygroscopicity of ADN is the key to realize the wide application of ADN.In this paper,we systematically review the research progress of anti-hygroscopic strategies of ADN coating.The surface coating methods are focusing on solvent volatilization,solvent-non-solvent,melt crystallization and atomic layer deposition technology.The characteristics of the different methods are compared and analyzed,and the basis for the classification and selection of the coating materials are introduced in detail.In addition,the feasibility of material for surface coating of ADN is evaluated by several compatibility analysis methods.It is highly expected that the liquid phase method(solvent volatilization method,solvent-non-solvent method)would be the promising method for future ADN coating because of its effective,safety and facile operation.Furthermore,polymer materials,are the preferred coating materials due to their high viscosity,easy adhesion,good anti-hygroscopic effect,and heat resistance,which make ADN weak hygroscopicity,less sensitive,easier to preserve and good compatibility.

New insights in nano-copper chromite catalyzing ultrafine AP:Evaluation of dispersity and mixing uniformity

Improving the application of nanomaterials has always been a research hotspot in the field of energetic materials(EMs)due to their obvious catalytic effect on the EMs,especially the uniformly dispersed nanomaterials.However,few studies have reported the dispersion of nanomaterials.In this study,the dispersity and mixing uniformity of nano-CuCr_(2)O_(4)was evaluated based on the difference of solid UV light absorption between the nano-catalytic materials and EMs.The nano-CuCr_(2)O_(4)/ultrafine AP composites with different dispersity of nano-CuCr_(2)O_(4)were prepared by manual grinding and mechanical grinding with different grinding strength and griding time.And then,the absorbance of different samples at 212 nm was obtained by solid UV testing due to the high repeatability of the absorbance at 210-214 nm for three parallel experiments,and the dispersity of different samples was calculated through the established difference equation.Furthermore,the samples were characterized by XRD,IR,SEM,EDS,DSC and TG-MS,which confirmed that different mixing methods did not change the structure of the samples(XRD and IR),and the mixing uniformity improved with the increase of grinding strength and grinding time(SEM and EDS).The scientificity and feasibility of the difference equation were further verified by DSC.The dispersity of nano-CuCr_(2)O_(4)exhibits a positive intrinsic relationship with its catalytic performance,and the uniformly dispersed nano-CuCr_(2)O_(4)significantly reduces the thermal decomposition temperature of ultrafine AP from 367.7 to 338.8℃.The TG-MS patterns show that the dispersed nano-CuCr_(2)O_(4)advanced the thermal decomposition process of ultrafine AP by about 700 s,especially in the high temperature decomposition stage,and the more concentrated energy release characteristic is beneficial to further enhance the energy performance of AP-based propellants.The above conclusions show that the evaluation method of dispersity based on solid UV curves could provide new ideas for the dispersity characterization of nano-catalytic materials in EMs,which is expected to be widely used in the field of EMs.

玻璃纤维板阵列增多层吸波复合结构

本文将电路模拟吸波阵列与玻璃纤维介质板(FEPL)阵列结合,采用真空热压成型工艺制备了一种具有超宽带强吸波性能的多层复合结构。整个FEPL阵列复合结构的表面密度约为2.4 kg/m^(2),厚度约为10.0 mm。仿真和测量结果均表明,FEPL阵列可以明显改善吸波结构的斜入射角的稳定性,提高电磁吸收率,拓宽吸收带宽。在斜入射角40°~60°范围内,FEPL阵列显著提高了吸波复合结构的吸收性能,同时将相对带宽(FBW)拓宽了约9.1%;此外,它还将复合吸波结构正入射角的平均反射系数从−14.4 dB降低到了−25.7 dB,降低了约11.3 dB。本文所提出的玻璃纤维板阵列增多层吸波复合结构性能优异,制备工艺简单,适合实际工程应用。

Understanding the dehydrogenation properties of Mg(0001)/MgH_(2)(110)interface from first principles

Magnesium hydride is one of the most promising solid-state hydrogen storage materials for on-board application.Hydrogen desorption from MgH_(2) is accompanied by the formation of the Mg/MgH_(2) interfaces,which may play a key role in the further dehydrogenation process.In this work,first-principles calculations have been used to understand the dehydrogenation properties of the Mg(0001)/MgH_(2)(110) interface.It is found that the Mg(0001)/MgH_(2)(110) interface can weaken the Mg-H bond.The removal energies for hydrogen atoms in the interface zone are significantly lower compared to those of bulk MgH_(2).In terms of H mobility,hydrogen diffusion within the interface as well as into the Mg matrix is considered.The calculated energy barriers reveal that the migration of hydrogen atoms in the interface zone is easier than that in the bulk MgH_(2).Based on the hydrogen removal energies and diffusion barriers,we conclude that the formation of the Mg(0001)/MgH_(2)(110) interface facilitates the dehydrogenation process of magnesium hydride.

Strain‑Induced Surface Interface Dual Polarization Constructs PML‑Cu/Bi_(12)O_(17)Br_(2) High‑Density Active Sites for CO_(2) Photoreduction

The insufficient active sites and slow interfacial charge trans-fer of photocatalysts restrict the efficiency of CO_(2) photoreduction.The synchronized modulation of the above key issues is demanding and chal-lenging.Herein,strain-induced strategy is developed to construct the Bi–O-bonded interface in Cu porphyrin-based monoatomic layer(PML-Cu)and Bi_(12)O_(17)Br_(2)(BOB),which triggers the surface interface dual polarization of PML-Cu/BOB(PBOB).In this multi-step polarization,the built-in electric field formed between the interfaces induces the electron transfer from con-duction band(CB)of BOB to CB of PML-Cu and suppresses its reverse migration.Moreover,the surface polarization of PML-Cu further promotes the electron converge in Cu atoms.The introduction of PML-Cu endows a high density of dispersed Cu active sites on the surface of PBOB,significantly promoting the adsorption and activation of CO_(2) and CO desorption.The conversion rate of CO_(2) photoreduction to CO for PBOB can reach 584.3μmol g-1,which is 7.83 times higher than BOB and 20.01 times than PML-Cu.This work offers valuable insights into multi-step polarization regulation and active site design for catalysts.

Purification process of coal-based coke powder as anode for Li-ion batteries

A process of purification of coal-based coke powder as anode for Li-ion batteries was attempted. The process started with the treatment of coke powder with dilute hydrofluoric acid solution, followed by united-acid-leaching using sulfuric acid and hydrochloric acid. The effects of altering the hydrofluoric acid addition, hydrofluoric acid concentration, contact time, temperature and acid type were investigated. A minimum ash content of 0.35% was obtained when proper conditions were applied. The electrochemical performance of purified coke powder shows greatly improved electrochemical performance. The as-purified coke powder presented an initial reversible capacity of 257.4 mAh/g and a retention rate of 95% after 50 cycles. The proposed purification process paves a way to prepare a promising anode material with good performance with low cost of coke powder for Li-ion batteries.

Effects of Metal and Composite Metal Nanopowders on the Thermal Decomposition of Ammonium Perchlorate (AP) and the Ammonium Perchlorate/Hydroxyterminated Polybutadiene (AP/HTPB) Composite Solid Propellant

Effects of metal (Ni, Cu, Al) and composite metal (NiB, NiCu, NiCuB) nanopowders on the thermal decomposition of ammonium perchlorate (AP) and composite solid propellant ammonium perchlorate/hydroxyterminated polybutadiene (AP/HTPB) were studied by thermal analysis (DTA). The results show that metal and composite metal nanopowders all have good catalytic effects on the thermal decomposition of AP and AP/HTPB composite solid propellant. The effects of metal nanopowders on the thermal decomposition of AP are less than those of the composite metal nanopowders. The effects of metal and composite metal nanopowders on the thermal decomposition of AP are different from those on the thermal decomposition of the AP/HTPB composite solid propellant.

One-Step Synthesis of Nanocrytalline Perovskite LaMnO_3 Powders via Microwave-Induced Solution Combustion Route

Perovskite LaMnO3 powders with an average crystallite size of 12.5 nm were rapidly synthesized via a microwave-induced autocombustion reaction using glycine as a fuel and nitrate as an oxidant. After self-propagating combustion, the desired nanocrystalline perovskite LaMnO3 was obtained and no further calcination was carried out. The possible processes of combustion reaction were discussed according to the principle of propellant chemistry. The autocombustion and thermal decomposition of the precursor were investigated using the TG-DTA and FT-IR techniques. The influences of glycine-nitrate molar ratio and heat-treatment temperature on the perovskite phase formation and crystallite size of as-burnt powder were studied by XRD. The morphology and size of the as-burnt powder before and after milling were characterized and compared by TEM.

Novel Salt-Assisted Combustion Synthesis of High Surface Area Ceria Nanopowders by An Ethylene Glycol-Nitrate Combustion Process

A novel salt-assisted combustion process with ethylene glycol as a fuel and nitrate as an oxidant to synthesize high surface area celia nanopowders was reported. The effects of various tunable conditions, such as fuel-to-oxidant ratio, type of salts, and amount of added salts, on the characteristics of the as-prepared powders were investigated by X-ray diffraction, transmission electron microscopy and BET surface area measurement. A mechanism scheme was proposed to illustrate the possible formation processes of well-dispersed ceria nanoparticles in the salt-assisted combustion synthesis. It was verified that the simple introduction of leachable inert inorganic salts as an excellent agglomeration inhibitor into the redox mixture precursor leads to the formation of well-dispersed ceria particles with particle size in the range of 4 ～6 nm and a drastic increase in the surface area. The presence of KCl results in an over ten-fold increment in specific surface area from 14.10 m^2·g^-1 for the produced ceria powders via the conventional combustion synthesis process to 156.74 m^2·g^-1 for the product by the salt-assisted combustion synthesis process at the same molar ratio of ethylene glycol-nitrate.

Fabrication of ultrafine Nd-Fe-B powder by a modified reduction-diffusion process

In order to obtain ultrafine Nd-Fe-B powder, a spray-dried precursor was treated by reduction-diffusion (R/D) process. And, unlike the conventional R/D process, calcium reduction that is a crucial step for the formation of Nd2Fe14B was performed without conglomerating the precursor with Ca powder. By adopting this modified process, it is possible to synthesize the hard magnetic Nd2Fe14B at the reaction temperature as low as 850 ℃. The average size of Nd2Fe14B particles that are uniformly distributed in the optimally treated powder was <<1 μm. Most Nd2Fe14B particles were enclosed with thin layers of Nd-rich phase. Typical magnetic properties of such powder without eliminating impurity CaO were iHc=～5.9 kOe, Br=～5.5 kG, and (BH)max=～6 MGOe.

Compaction of TiAlMn Alloy Powder by Explosion and Sintering

Direct explosive compaction and sintering of a mixture of Ti-30Al-2Mn(wt%)and Ti-38Al-2Mn(wt%) intermetallic compound powders were carried out.Microstructure and phase characteristics of the alloys were analysed by TEM,SEM,X-ray diffractometry and optical microscopy.The results showed that the rel- ative density of the samples which were explosive-compacted and sintered reached 99.90%,and fine grain structure was obtained.Through the explosive-compacting and then sintering at 1373 K in argon atmos- phere,mutual diffusion between Ti-30Al-2Mn particles and Ti-38Al-2Mn particles took place and TiAl phase was formed in the alloy.TiAl based alloys prepared by high-energy ball-milling powders had much fi- ner grain size than those prepared by general ball-milling powdeis.

GO/HTPB composite liner for anti-migration of small molecules

Hydroxyl-terminated polybutadiene/toluene diisocyanate(HTPB/TDI)system is widely used in composite solid propellants.The migrations of plasticizers and water molecules from solid propellants and surrounding environment to the inhibitor have always been the important issues.This study focuses on the preparation,characterization and anti-migration behavior of graphene oxide(GO)/HTPB nanocomposite liner.The GO/HTPB(GH)composite liners affect the migration of small molecules through a tighter cross-linked structure and weakening function of small molecule adsorption.The anti-migration performance of the liner at different temperatures was analyzed,and the influence of the added amount of GO on the anti-migration performance and adhesion performance was also systematically studied.The overall performance of the liner is optimized when the amount of GO filler is 0.3 wt%.After adding 0.3 wt%GO,the concentration of dioctyl sebacate(DOS)migrated into the liner is decreased by 23.28%,and the concentration of water molecules is decreased by 51.89%,indicating that the introduction of GO can significantly improve the anti-migration performance of the liner.In addition,the bond strength is greatly increased from 0.25 MPa to 0.95 MPa,which meets the application requirements of the current propellant system.This research provides an important way for the preparation of structure-function synergistic anti-migration composite liners.

铵盐溶液中一水合三氧化钨直接转型制备仲钨酸铵

针对目前四水合仲钨酸铵生产和开发过程中存在流程长、能源消耗高、钨结晶率低和环境污染严重等问题,本文开发了一种经济、高效、可持续的技术直接转型制备四水合仲钨酸铵。结果表明,在不同的实验条件下,原料一水合三氧化钨与碳酸氢铵或碳酸铵按生成仲钨酸铵的化学计量配比,可在密闭容器中进行直接转化得到仲钨酸铵产品。控制反应条件为:温度80℃,液固质量比2:1,添加剂PEG2000加入量80×10-6g/L,固相一水合三氧化钨与碳酸氢铵溶液反应3 h。制备出的四水合仲钨酸铵产品颗粒表面致密,平均粒径为61.7μm。转型得到的仲钨酸铵产品化学纯度符合APT·4H2O-0级品标准。

Layer-Contacted Graphene-Like BN/Ultrathin Bi_(3)O_(4)Br Stacking for Boosting Photocatalytic Molecular Oxygen Activation

Novel graphene-like boron nitride(BN)/Bi_(3)O_(4)Br photocatalysts have been controllably synthesized through a facile solvothermal method for the first time. Layer contact stacking between graphene-like BN and ultrathin Bi_(3)O_(4)Br was achieved with strong interaction. Dehalogenation is designed to harvest more visible light, and the ultrathin structure of Bi_(3)O_(4)Br is designed to accelerate charge transfer from inside to the surface. After graphene-like BN was engineered, photocatalytic performance greatly improved under visible light irradiation. Graphene-like BN can act as a surface electron-withdrawing center and adsorption center, facilitating molecular oxygen activation. O_(2)^(·-)was determined to be the main active species during the degradation process through analyses of electron spin resonance and XPS valence band spectra.

Oxygen defect modulating the charge behavior in titanium dioxide for boosting photocatalytic nitrogen fixation performance

Extremely high-temperature and high-pressure requirement of Haber-Bosch process motivates the search for a sustainable ammonia synthesis approach under mild conditions.Photocatalytic technology is a potential solution to convert N2 to ammonia.However,the poor light absorption and low charge carrier separation efficiency in conventional semiconductors are bottlenecks for the application of this technology.Herein,a facile synthesis of anatase TiO_(2)nanosheets with an abundance of surface oxygen vacancies(TiO_(2)-OV)via the calcination treatment was reported.Photocatalytic experiments of the prepared anatase TiO_(2)samples showed that TiO_(2)-OV nanosheets exhibited remarkably increased ammonia yield for solar-driven N2 fixation in pure water,without adding any sacrificial agents.EPR,XPS,XRD,UV-Vis DRS,TEM,Raman,and PL techniques were employed to systematically explore the possible enhanced mechanism.Studies revealed that the introduced surface oxygen vacancies significantly extended the light absorption capability in the visible region,decreased the adsorption and activation barriers of inert N2,and improved the separation and transfer efficiency of the photogenerated electronhole pairs.Thus,a high rate of ammonia evolution in TiO_(2)-OV was realized.This work offers a promising and sustainable approach for the efficient artificial photosynthesis of ammonia.

193 nm激光对MgF_(2)窗口材料的损伤特性研究

随着光刻技术和低温硅退火等大能量、高功率紫外激光系统的发展,激光装置中窗口材料面临的紫外激光诱导损伤的问题越来越得到重视。MgF_(2)窗口是紫外波段难以替代的光学窗口材料,具有比CaF_(2)更优的紫外透光率、更低的折射率和更高的硬度等优点,因而在高功率紫外激光器、深紫外探测器、光电探测和对抗领域具有重要的应用。研究激光对MgF_(2)窗口材料的损伤机制对推动其在光学领域的应用至关重要。本文通过扫描电镜分析MgF_(2)窗口材料在193 nm紫外激光(2.8 J/cm^(2))辐照下出现的裂纹和凹坑等损伤形貌,随着激光脉冲数和能量的增加,MgF_(2)窗口材料的后表面损伤程度呈指数级增加,窗口材料的后表面损伤程度比前表面更加严重。利用三维时域有限差分(3D-FDTD)方法对193 nm激光辐照MgF_(2)窗口材料内部的激光电场分布进行了计算。模拟发现无论缺陷在前表面还是后表面,电场强度的峰值都出现在后表面附近,后表面更容易被损伤,这与实验结果吻合;缺陷在激光辐照过程中会导致光场的局域调制,增强吸收,同时降低材料表面的机械强度。

Structural regulation chemistry of lithium-ion solvation in nonflammable phosphate-based electrolytes for high interfacial compatibility with graphite anode

With the booming development of lithium-ion batteries,safety has become one of the most primary focuses of current researches.Although there are various approaches to enhance the safety of lithiumion batteries,phosphate-based electrolyte holds the greatest potential for practical application due to their non-flammability.Nonetheless,its compatibility issue with the graphite anode remains a significant obstacle to its widespread use.Herein,an effective method is proposed to improve the compatibility of electrolyte with graphite(Gr)anode by rationally adjusting the proportion of lithium salt and solvent components to optimize the Li^(+)solvation structure.By slightly increasing the Li^(+)/triethyl phosphate(TEP)ratio,TEP alone cannot fully occupy the inner solvation sheath and therefore less polar ethylene carbonate(EC)has to be recruited,and the solvation structure gradually changes from Li^(+)–[TEP]_(4)to Li^(+)–[TEP]_(3)[EC]with the coexistence of EC and TEP.Simultaneously,EC molecules in the Li^(+)–[TEP]_(3)[EC]could be preferentially reduced on graphite compared to the TEP molecules,resulting in the formation of a uniform and durable solid-electrolyte interphase(SEI)layer.Benefiting from the optimized phosphate-based electrolyte,the Gr|Li battery exhibits a capacity retention rate of 96.8%after stable cycling at 0.5 C for 470 cycles which shows a longer cycle life than the battery with carbonate electrolyte(cycling at 0.5 C for 450 cycles).Therefore,this work provides the guidance for designing a non-flammable phosphate-based electrolyte for high-safety and long cycling-life lithium-ion batteries.

Study of nano-nitramine explosives:preparation,sensitivity and application

Nano-nitramine explosives(RDX.HMX.CL-20) are produced on a bi-directional grinding mill.The scanning electron microscope(SEM)observations show that the prepared particles are semi-spherical,and the narrow size distributions are characterized using the laser particle size analyzer.Compared with the micron-sized samples,the nano-products show obvious decrease in friction and impact sensitivities.In the case of shock sensitivities,nano-products have lower values by 59.9%(RDX),56.4%(HMX),and 58.1%(CL-20),respectively.When nano-RDX and nano-HMX are used in plastic bonded explosives(PBX) as alternative materials of micron-sized particles,their shock sensitivities are significantly decreased by 24.5%(RDX) and 22.9%(HMX),and their detonation velocities are increased by about 1.7%.Therefore,it is expected to promote the application of nano-nitramine explosives in PBXs and composite modified double-based propellants(CMDBs) so that some of their properties would be improved.

Effect of Drying on Particle Size and Sensitivities of Nano hexahydro-1,3,5-trinitro-1,3,5-triazine

Nano hexahydro-1,3,5-trinitro-1,3,5-triazine(RDX) was prepared using a bi-directional rotation mill and dried under different conditions(liquid, temperature and drying). It shows that the samples cake seriously and the particles grow up obviously by ordinary drying in different liquids at 70 C, which occurs again after vacuum drying. With the increase of temperature, the degrees of caking and aggregation are enhanced.Well dispersed sample maintaining constant particle size is extracted by supercritical drying, especially freeze drying. Furthermore, the mechanical sensitivities of I-RDX, O-RDX and F-RDX, of which the average sizes are 88.03 mm, 15.32 mm and 0.16 mm, respectively, are evaluated. Compared with I-RDX, the friction, impact and shock sensitivities of O-RDX are slightly lower. However, the friction, impact and shock sensitivities of F-RDX are reduced by 30%, 99.0% and 59.9%, respectively.