基于蒙特卡罗模拟的透射式XRD背景的定量分析

XRD背景主要来源于空气、装置和样品中光子的散射,XRD分析需准确扣除背景,常用的扣背景方法具有一定的局限。蒙特卡罗模拟可实现光子的甄别与统计,因此可将其用于XRD背景来源的定量分析。相干散射的模拟中需考虑物质的Form Factor,这可由Baró等的拟合式、独立原子模型或德拜公式给出;在20 keV能量及透射几何模式下,通过对骨、尼龙、水等物质的XRD模拟,对探测器中光子来源进行了区分和统计。结果表明,德拜公式计算的空气背景大于独立原子模型;空气散射在小角度时背景占比大,随散射角的增加从100%减小至40%以下,而样品中康普顿散射的计数占比则从0增大至60%以上。该方法可对不同样品组成以及复杂装置结构的XRD背景进行定量分析。

偏光显微镜和XRD在南非Postmasburg锰矿定性分析中的应用

根据南非Postmasburg锰矿田BIF型矿体中的矿石分带和品位差异,识别出了富锰型矿石、砾岩型矿石以及铁质岩型矿石。为确定各类矿石的矿物成分,了解矿石类型与其矿物成分间的对应关系,以各类矿石为研究对象,对其中的矿物成分进行了研究。采用偏光显微鉴定技术结合X射线衍射物相分析,基于矿物偏光特征和特征衍射峰,对矿石中的矿物进行了定性。结果表明,富锰型矿石中的主量矿物为方铁锰矿和褐锰矿;砾岩型矿石中金属矿物几乎全为赤铁矿,黏土矿物以钠珠云母为主;含砾铁质岩中黏土矿物居多,以白云母为主,金属矿物多为赤铁矿。由此可见,偏光显微鉴定和XRD具有良好的一致性和互补性,尤其是对厚层的沉积型矿床,岩性和岩相具有一定变化序列的情况下,更适合二者相结合进行精确定性分析。

Assessing the conservation impact of Chinese indigenous chicken populations between ex-situ and in-situ using genome-wide SNPs

Conservation programs require rigorous evaluation to ensure the preservation of genetic diversity and viability of conservation populations. In this study, we conducted a comparative analysis of two indigenous Chinese chicken breeds, Gushi and Xichuan black-bone, using whole-genome SNPs to understand their genetic diversity, track changes over time and population structure. The breeds were divided into five conservation populations(GS1, 2010, ex-situ;GS2, 2019, ex-situ;GS3, 2019, in-situ;XB1, 2010, in-situ;and XB2, 2019, in-situ) based on conservation methods and generations. The genetic diversity indices of three conservation populations of Gushi chicken showed consistent trends, with the GS3 population under in-situ strategy having the highest diversity and GS2 under ex-situ strategy having the lowest. The degree of inbreeding of GS2 was higher than that of GS1 and GS3. Conserved populations of Xichuan black-bone chicken showed no obvious changes in genetic diversity between XB1 and XB2. In terms of population structure, the GS3 population were stratified relative to GS1 and GS2. According to the conservation priority, GS3 had the highest contribution to the total gene and allelic diversity in GS breed, whereas the contribution of XB1 and XB2 were similar. We also observed that the genetic diversity of GS2 was lower than GS3, which were from the same generation but under different conservation programs(in-situ and ex-situ). While XB1 and XB2 had similar levels of genetic diversity. Overall, our findings suggested that the conservation programs performed in ex-situ could slow down the occurrence of inbreeding events, but could not entirely prevent the loss of genetic diversity when the conserved population size was small, while in-situ conservation populations with large population size could maintain a relative high level of genetic diversity.

In-situ AFM and quasi-in-situ studies for localized corrosion in Mg-9Al-1Fe-(Gd) alloys under 3.5 wt.% NaCl environment

Revealing the localized corrosion process of Mg alloy is considered as one of the most significant ways for improving its corrosion resistance.The reliable monitor should be high distinguishability and real-time in liquid environment.Herein,Mg-9Al-1Fe and Mg-9Al-1Fe-1Gd alloys were designed to highlight the impact of intermetallic on the corrosion behaviour.In-situ AFM with a special electrolyte circulation system and quasi-in-situ SEM observation were used to monitor the corrosion process of the designed alloys.SEM-EDS and TEM-SAED were applied to identify the intermetallic in the designed alloys,and their volta potentials were measured by SKPFM.According to the real-time and real-space in-situ AFM monitor,the corrosion process consisted of dissolution of anodicα-Mg phase,accumulation of corrosion products around cathodic phase and shedding of some fine cathodic phase.Then,the localized corrosion process of Mg alloy was revealed combined with the results of the monitor of corrosion process and Volta potential difference.

An in-situ study of static recrystallization in Mg using high temperature EBSD

It has been a common method to improve the mechanical properties of metals by manipulating their microstructures via static recrystallization,i.e.,through heat treatment.Therefore,the knowledge of recrystallization and grain growth is critical to the success of the technique.In the present work,by using in-situ high temperature EBSD,the mechanisms that control recrystallization and grain growth of an extruded pure Mg were studied.The experimental results revealed that the grains of priority for dynamic recrystallization exhibit fading competitiveness under static recrystallization.It is also found that grain boundary movement or grain growth is likely to show an inverse energy gradient effect,i.e.,low energy grains tend to swallow or grow into high energy grains,and grain boundaries of close to 30°exhibit superior growth advantage to others.Another finding is that{10-12}tensile twin boundaries are sites of hardly observed for recrystallization,and are finally swallowed by adjacent recrystallized grains.The above findings may give comprehensive insights of static recrystallization and grain growth of Mg,and may guide the design of advanced materials processing in microstructural engineering.

An in-situ self-etching enabled high-power electrode for aqueous zinc-ion batteries

Sluggish storage kinetics is considered as the main bottleneck of cathode materials for fast-charging aqueous zinc-ion batteries(AZIBs).In this report,we propose a novel in-situ self-etching strategy to unlock the Palm tree-like vanadium oxide/carbon nanofiber membrane(P-VO/C)as a robust freestanding electrode.Comprehensive investigations including the finite element simulation,in-situ X-ray diffraction,and in-situ electrochemical impedance spectroscopy disclosed it an electrochemically induced phase transformation mechanism from VO to layered Zn_(x)V_(2)O_5·nH_(2)O,as well as superior storage kinetics with ultrahigh pseudocapacitive contribution.As demonstrated,such electrode can remain a specific capacity of 285 mA h g^(-1)after 100 cycles at 1 A g^(-1),144.4 mA h g^(-1)after 1500 cycles at 30 A g^(-1),and even 97 mA h g^(-1)after 3000 cycles at 60 A g^(-1),respectively.Unexpectedly,an impressive power density of 78.9 kW kg^(-1)at the super-high current density of 100 A g^(-1)also can be achieved.Such design concept of in-situ self-etching free-standing electrode can provide a brand-new insight into extending the pseudocapacitive storage limit,so as to promote the development of high-power energy storage devices including but not limited to AZIBs.

Microstructural characterization and mechanical properties of(TiC+TiB)/TA15 composites prepared by an in-situ synthesis method

Titanium matrix composites reinforced with ceramic particles are considered a promising engineering material due to their combination of high specific strength,low density,and high modulus.In this study,the TA15-based composites reinforced with a volume fraction of 10% to 25%(TiB+TiC)were prepared using powder metallurgy and casting technique.Microstructural characterization and phase constitution were examined using optical microscopy(OM),scanning electron microscopy(SEM),and X-ray diffraction(XRD).In addition,the microhardness,room temperature(RT)and high temperature(HT)tensile properties of the composites were evaluated.Results revealed that the reinforcements are distributed uniformly even in the composites with a high volume of TiB and TiC.However,as the volume fraction exceeds 15%,TiB and TiC particles become coarsening and exhibit rod-like and dendritic-like morphology.Microhardness increases gradually from 321.2 HV for the base alloy to a maximum of 473.3 HV as the reinforcement increases to 25vol.%.Tensile test results indicate that a reinforcement volume fraction above 20% is beneficial for enhancing tensile strength and yield strength at high temperatures,but it has an adverse effect on room temperature elongation.Conversely,if the reinforcement volume fraction is below 20%,it can improve high-temperature elongation when the temperature exceeds 600℃.

Progress in in-situ electrochemical nuclear magnetic resonance for battery research

A thorough understanding of the fundamental electrochemical and chemical processes in batteries is crucial to advancing energy density and power density.However,the characterizations of such processes are complex.In-situ electrochemical nuclear magnetic resonance(EC-NMR)offers the capability to collect real-time data during battery operation,furnishing insights into the local structures and ionic dynamics of materials by monitoring changes in the chemical environment around the nuclei.EC-NMR also has the advantages of being both quantitative and non-destructive.This paper systematically reviews the design of EC-NMR approach,and delves into the applications and progress of EC-NMR concerning battery reaction mechanisms,failure mechanisms,and overall battery systems.The review culminates in a comprehensive summary of the perspective and challenges associated with EC-NMR.

In-situ polymerized PEO-based solid electrolytes contribute better Li metal batteries:Challenges,strategies,and perspectives

Polyethylene oxide(PEO)-based solid polymer electrolytes(SPEs)with good electrochemical stability and excellent Li salt solubility are considered as one of the most promising SPEs for solid-state lithium metal batteries(SSLMBs).However,PEO-based SPEs suffer from low ionic conductivity at room temperature and high interfacial resistance with the electrodes due to poor interfacial contact,seriously hindering their practical applications.As an emerging technology,in-situ polymerization process has been widely used in PEO-based SPEs because it can effectively increase Li-ion transport at the interface and improve the interfacial contact between the electrolyte and electrodes.Herein,we review recent advances in design and fabrication of in-situ polymerized PEO-based SPEs to realize enhanced performance in LMBs.The merits and current challenges of various SPEs,as well as their stabilizing strategies are presented.Furthermore,various in-situ polymerization methods(such as free radical polymerization,cationic polymerization,anionic polymerization)for the preparation of PEO-based SPEs are summarized.In addition,the application of in-situ polymerization technology in PEO-based SPEs for adjustment of the functional units and addition of different functional filler materials was systematically discussed to explore the design concepts,methods and working mechanisms.Finally,the challenges and future prospects of in-situ polymerized PEO-based SPEs for SSLMBs are also proposed.

In-situ interfacial passivation and self-adaptability synergistically stabilizing all-solid-state lithium metal batteries

The function of solid electrolytes and the composition of solid electrolyte interphase(SEI)are highly significant for inhibiting the growth of Li dendrites.Herein,we report an in-situ interfacial passivation combined with self-adaptability strategy to reinforce Li_(0.33)La_(0.557)TiO_(3)(LLTO)-based solid-state batteries.Specifically,a functional SEI enriched with LiF/Li_(3)PO_(4) is formed by in-situ electrochemical conversion,which is greatly beneficial to improving interface compatibility and enhancing ion transport.While the polarized dielectric BaTiO_(3)-polyamic acid(BTO-PAA,BP)film greatly improves the Li-ion transport kinetics and homogenizes the Li deposition.As expected,the resulting electrolyte offers considerable ionic conductivity at room temperature(4.3 x 10~(-4)S cm^(-1))and appreciable electrochemical decomposition voltage(5.23 V)after electrochemical passivation.For Li-LiFePO_(4) batteries,it shows a high specific capacity of 153 mA h g^(-1)at 0.2C after 100 cycles and a long-term durability of 115 mA h g^(-1)at 1.0 C after 800 cycles.Additionally,a stable Li plating/stripping can be achieved for more than 900 h at 0.5 mA cm^(-2).The stabilization mechanisms are elucidated by ex-situ XRD,ex-situ XPS,and ex-situ FTIR techniques,and the corresponding results reveal that the interfacial passivation combined with polarization effect is an effective strategy for improving the electrochemical performance.The present study provides a deeper insight into the dynamic adjustment of electrode-electrolyte interfacial for solid-state lithium batteries.

准东阜康凹陷XRD录井多层感知器法储层物性评价探索

快速准确评价储层物性是试油选层及压裂定段的关键。为研究准东阜康凹陷二叠系上乌尔禾组优质储层分布层段,探索了多层感知器法在准东阜康凹陷XRD录井储层物性评价中的应用。通过收集大量的XRD录井数据,优选5种特征矿物构建多层感知器法神经网络模型,验证发现所建立的模型能够较好地拟合储层物性参数与矿物含量之间的关系。经过训练的模型在测试数据集上取得了较高的预测准确率,为快速、准确评价储层物性提供了新途径。在KT 5及F 47井应用取得了较好的评价效果,具有一定的推广应用价值。

Interplay of laser power and pore characteristics in selective laser melting of ZK60 magnesium alloys:A study based on in-situ monitoring and image analysis

This study offers significant insights into the multi-physics phenomena of the SLM process and the subsequent porosity characteristics of ZK60 Magnesium(Mg)alloys.High-speed in-situ monitoring was employed to visualise process signals in real-time,elucidating the dynamics of melt pools and vapour plumes under varying laser power conditions specifically between 40 W and 60 W.Detailed morphological analysis was performed using Scanning-Electron Microscopy(SEM),demonstrating a critical correlation between laser power and pore formation.Lower laser power led to increased pore coverage,whereas a denser structure was observed at higher laser power.This laser power influence on porosity was further confirmed via Optical Microscopy(OM)conducted on both top and cross-sectional surfaces of the samples.An increase in laser power resulted in a decrease in pore coverage and pore size,potentially leading to a denser printed part of Mg alloy.X-ray Computed Tomography(XCT)augmented these findings by providing a 3D volumetric representation of the sample internal structure,revealing an inverse relationship between laser power and overall pore volume.Lower laser power appeared to favour the formation of interconnected pores,while a reduction in interconnected pores and an increase in isolated pores were observed at higher power.The interplay between melt pool size,vapour plume effects,and laser power was found to significantly influence the resulting porosity,indicating a need for effective management of these factors to optimise the SLM process of Mg alloys.

Oxidation of emerging organic contaminants by in-situ H_(2)O_(2) fenton system

The existence and risk of emerging organic contaminants(EOCs)have been under consideration and paid much effort to degrade these pollutants.Fenton system is one of the most widely used technologies to solve this problem.The original Fenton system relies on the hydroxyl radicals produced by Fe(Ⅱ)/H_(2)O_(2) to oxidize the organic contaminants.However,the application of the Fenton system is limited by its low iron cycling efficiency and the high risks of hydrogen peroxide transportation and storage.The introduction of external energy(including light and electricity etc.)can effectively promote the Fe(Ⅲ)/Fe(Ⅱ)cycle and the reduction of oxygen to produce hydrogen peroxide in situ.This review introduces three in-situ Fenton systems,which are electro-Fenton,Photo-Fenton,and chemical reaction.The mechanism,influencing factors,and catalysts of these three in-situ Fenton systems in degrading EOCs are discussed systematically.This review strengthens the understanding of Fenton and in-situ Fenton systems in degradation,offering further insight into the real application of the in-situ Fenton system in the removal of EOCs.

In-situ coating and surface partial protonation co-promoting performance of single-crystal nickel-rich cathode in all-solid-state batteries

The poor electrochemical performance of all-solid-state batteries(ASSBs),which is assemblied by Ni-rich cathode and poly(ethylene oxide)(PEO)-based electrolytes,can be attributed to unstable cathodic interface and poor crystal structure stability of Ni-rich cathode.Several coating strategies are previously employed to enhance the stability of the cathodic interface and crystal structure for Ni-rich cathode.However,these methods can hardly achieve simplicity and high efficiency simultaneously.In this work,polyacrylic acid(PAA)replaced traditional PVDF as a binder for cathode,which can achieve a uniform PAA-Li(LixPAA(0<x≤1))coating layer on the surface of single-crystal LiNi_(0.83)Co_(0.12)Mn_(0.05)O_(2)(SC-NCM83)due to H^(+)/Li^(+)exchange reaction during the initial charging-discharging process.The formation of PAA-Li coating layer on cathode can promote interfacial Li^(+)transport and enhance the stability of the cathodic interface.Furthermore,the partially-protonated surface of SC-NCM83 casued by H^(+)/Li^(+)exchange reaction can restrict Ni ions transport to enhance the crystal structure stability.The proposed SC-NCM83-PAA exhibits superior cycling performance with a retention of 92%compared with that(57.3%)of SC-NCM83-polyvinylidene difluoride(PVDF)after 200 cycles.This work provides a practical strategy to construct high-performance cathodes for ASSBs.

FTIR和XRD在断层构造煤结构分析中的应用

为探究断层构造作用对煤化学结构特征和微晶结构特征的影响,采用傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)分析,对红庆梁矿和段王矿的原生煤及断层构造煤进行分析。结果表明,受断层构造作用影响,红庆梁、段王断层构造煤中苯环二取代、苯环四取代的含量明显大于原生煤,苯环三取代和苯环五取代的含量低于原生煤,断层构造煤中C—O—C伸缩振动、—CH_(2)反对称弯曲振动、—CH_(3)、—CH_(2)和芳环—OH含量均多于原生煤,断层构造煤中醚C—O振动、芳烃CC、—CH和OH—π含量低于原生煤。红庆梁、段王断层构造煤的芳碳率fa是原生煤的1.01和1.03倍,芳环缩合度DOC是原生煤的1.01倍和3.7倍,CH_(2)/CH_(3)值是原生煤样的0.933倍和0.94倍,芳香度I分别是原生煤样的1.01倍和1.34倍。说明断层构造作用促使官能团和脂肪链脱落,增加煤的缩聚程度,降低煤中脂肪侧链的长度,增大芳香结构含量。XRD测试结果表明,原生煤和断层构造煤具有相近的矿物组分,断层构造作用未对煤中矿物组分的类型产生明显的改变。在2θ=26°附近存在特征(002)带,表明存在少量的层状石墨结构,然而在2θ=45°附近并没有清楚地显示(100)带,说明煤中石墨结构的基面生长水平较低。红庆梁、段王断层构造煤的晶间间距d_(002)值与原生煤相比变化很小,微晶堆积高度L_(c)值分别是原生煤的0.9045倍和0.9027倍,芳香度f_(a)-XRD值分别是原生煤的1.1439倍和1.0669倍,晶体堆叠平均层数N_(ave)值分别是原生煤的0.90945倍和0.92356倍。断层构造作用减小煤的芳香层片堆砌度,增大煤的芳香度,减少了煤微晶结构单元的堆叠层数,说明断层构造促进煤中非芳香化合物向芳香化合物的转化。断层构造煤的芳香度、成熟度更高,断层构造煤的燃烧反应性弱于原生煤。

高校化学TGA、SEM和XRD的微视频教学探索

高校化学专业实验为研究性教学的重要环节,既承担知识和技能的传授,同时启迪学生的创造性思维并提升其素质。后疫情时期,开展大学化学专业实验混合式教学模式势在必行。作为一种多功能、性能优良的无机化学材料,纳米氧化锌被科学家们持续关注。以掺铝氧化锌(ZAO)为例介绍表征其结构、形貌和热失重的三种大型仪器的操作短视频制作:热失重分析仪(TGA)、飞纳扫描电子显微镜(SEM)和X射线粉末衍射仪(XRD)。期待为新冠肺炎疫情常态化防控背景下,高校化学专业实验、创新实验和科普平台的建立提供素材及方法借鉴。

In-situ observations of damage-fracture evolution in surrounding rock upon unloading in 2400-m-deep tunnels

The damage-fracture evolution of deep rock mass has obvious particularity,which is revealed in 2400-mdeep tunnels by field tests.The evolution of the excavation damaged zone depth is consistent with that of the fractured zone depth.The ratio of the excavation damaged zone depth to the excavation fractured zone depth is greater than 2.0 in a rock mass with both high strength and good integrity,but less than1.5 in a rock mass with lower strength or poor integrity.Zonal disintegration in a rock mass with high strength and fair integrity is more likely to occur when it contains more than two groups of primary fractures in damaged zones.Fractures develop outward in zonal disintegration but are totally different from the single-zone fracture,in which the fractures develop inward,and it is the starting position of the fractured zone when the excavation surface of the middle pilot is 7–9 m close to the pre-set borehole and it stops after the excavation surface of the baseplate is 11–14 m away.The most intense evolution occurs around 2–4 m from the pre-set borehole in the sidewall expansion stage.The research results provide a reference for the monitoring scheme and support design of CJPL-Ⅲin its future construction.

Application of Mythen detector:In-situ XRD study on the thermal expansion behavior of metal indium

A Mythen detector has been equipped at the beamline 4B9 A of Beijing Synchrotron Radiation Facility(BSRF),which is expected to enable BSRF to perform time-resolved measurement of X-ray diffraction(XRD) full-profiles.In this paper,the thermal expansion behavior of metal indium has been studied by using the in-situ XRD technique with the Mythen detector.The indium was heated from 303 to 433 K with a heating rate of 2 K/min.The in-situ XRD full-profiles were collected with a rate of one profile per 10 seconds.Rietveld refinement was used to extract the structural parameters.The results demonstrate that these collected quasi-real-time XRD profiles can be well used for structural analysis.The metal indium was found to have a nonlinear thermal expansion behavior from room temperature to the melting point(429.65 K).The a-axis of the tetragonal unit cell expands with a biquadratic dependency on temperature,while the c-axis contracts with a cubic dependency on temperature.By the time-resolved XRD measurements,it was observed that the[200]preferred orientation can maintain to about 403.15 K.While(110) is the last and detectable crystal plane just before melting of the polycrystalline indium foil.This study is not only beneficial to the application of metal indium,but also exhibits the capacity of in-situ time-resolved XRD measurements at the X-ray diffraction station of BSRF.

Fabrication of ZIF-8 membranes on dual-layer ZnO-PES/PES organic hollow fibers by in-situ crystallization

Compared to inorganic supports, polymeric supports can offer additional benefits, e.g., easier processing and cheaper. However, the organic surface has weak adhesion to the zeolitic imidazolate frameworks(ZIFs) membrane layer, which usually requires complex surface modification or seeding. Herein, we demonstrate that a dual-layer asymmetric polymer support prepared by a simple spinning process is a good candidate for the preparation of ZIF-8 membrane. The inner layer of the support is an organic hollow fiber(PES) with finger-like pores, and the outer layer is a ZnO-PES composite layer with finger-like pores also. The ZnO-PES composite layer is expected to contain uniform ZnO crystals in the polymer matrix, i.e., the ZnO particles in the skin layer of the support are not easy to fall off. Under the induction of ZnO particles in the outer layers, continuous ZIF-8 membranes can be prepared by single in-situ crystallization, showing good adhesion to the supports. The obtained ZIF-8 membranes show a H_(2) permeance of 8.7 × 10^(-8)mol·m^(-2)·s^(-1)·Pa^(-1) with a H_(2)/N_(2) ideal separation selectivity of 18.0. The design and preparation of this dual-layer polymer support is expected to promote the large-scale application of MOF membranes on polymer supports.

X射线衍射(XRD)定量分析铜闪速吹炼渣中磁铁尖晶石含量

为提高铜闪速吹炼渣磁铁尖晶石含量测量方法的稳定性和实用性,以铜闪速吹炼渣为研究对象,基于XRD定量分析原理,分别采用内标法和K值法测量闪速吹炼渣中磁铁尖晶石含量,同时对比化学物相分析法、扫描电子显微镜(SEM)照片面积统计分析法、饱和磁性仪定量测定结果,评价各方法的优劣。XRD定量分析测得样品中磁铁尖晶石含量结果:内标法16.78%,测量误差≤0.15%;K值法17.80%。对比其他分析方法具有更小的测量误差和更高的稳定性。方法的建立,可为开发铜冶炼渣中高效、稳定、便捷的磁铁尖晶石含量分析检测方法提供新思路。