Statistical model for combustion of high-metal magnesium-based hydro-reactive fuel

We investigate experimentally and analytically the combustion behavior of a high-metal magnesium-based hydro- reactive fuel under high temperature gaseous atmosphere. The fuel studied in this paper contains 73% magnesium powders. An experimental system is designed and experiments are carried out in both argon and water vapor atmo- spheres. It is found that the burning surface temperature of the fuel is higher in water vapor than that in argon and both of them are higher than the melting point of magnesium, which indicates the molten state of magnesium particles in the burning surface of the fuel. Based on physical considerations and experimental results, a mathematical one-dimensional model is formulated to describe the combustion behavior of the high-metal magnesium-based hydro-reactive fuel. The model enables the evaluation of the burning surface temperature, the burning rate and the flame standoff distance each as a function of chamber pressure and water vapor concentration. The results predicted by the model show that the burning rate and the surface temperature increase when the chamber pressure and the water vapor concentration increase, which are in agreement with the observed experimental trends.

Unlock the full potential of carbon cloth-based scaffolds towards magnesium metal storage via regulation on magnesiophilicity and surface geometric structure

The development of rechargeable magnesium(Mg) batteries is of practical significance to upgrade the electric energy storage devices due to exceptional capacity and abundant resources of Mg-metal anode.However,the reversible Mg electrochemistry suffers from unsatisfied rate capability and lifespan,mainly caused by non-uniform distribution of electrodeposits.In this work,a fresh design concept of threedimensional carbon cloths scaffolds is proposed to overcome the uncontrollable Mg growth via homogenizing electric field and improving magnesiophilicity.A microscopic smooth and nitrogen-containing defective carbonaceous layer is constructed through a facile pyrolysis of ZIF8 on carbon cloths.As revealed by finite element simulation and DFT calculation results,the smooth surface endows with uniform electric field distribution and simultaneously the nitrogen-doping species enable good magnesiophilicity of scaffolds.The fine and uniform Mg nucleus as well as the inner electrodeposit behavior are also disclosed.As a result,an exceptional cycle life of 500 cycles at 4.0 mA cm^(-2) and 4.0 mA h cm^(-2) is firstly realized to our best knowledge.Besides,the functional scaffolds can be cycled for over 2200 h at 2.0 mA cm^(-2) under a normalized capacity of 5.0 mA h cm^(-2),far exceeding previous results.This work offers an effective approach to enable the full potential of carbon cloths-based scaffolds towards metal storage for next generation battery applications.

Uniform nanoplating of metallic magnesium film on titanium dioxide nanotubes as a skeleton for reversible Na metal anode

To meet the low-cost concept advocated by the sodium metal anode,this paper reports the use of a pulsed electrodeposition technology with ionic liquids as electrolytes to achieve uniform nanoplating of metallic magnesium films at around 20 nm on spaced titanium dioxide(TiO_(2))nanotubes(STNA-Mg).First,the sodiophilic magnesium metal coating can effectively reduce the nucleation overpotential of sodium metal.Moreover,three-dimensional STNA can limit the volume expansion during sodium metal plating and stripping to achieve the ultrastable deposition and stripping of sodium metals with a high Coulombic efficiency of up to 99.5%and a small voltage polarization of 5 mV in symmetric Na||Na batteries.In addition,the comparative study of sodium metal deposition behavior of STNA-Mg and STNA-Cu prepared by the same route further confirmed the advantage of magnesium metal to guide sodium metal growth.Finally,the prepared STNA-Mg-Na metal anode and commercial sodium vanadium phosphate cathode were assembled into a full cell,delivering a discharge capacity of 110.2 mAh·g^(-1)with a retention rate of 95.6%after 110 cycles at 1C rate.

Hybrid solid electrolyte interphases formed in conventional carbonate electrolyte enable high-voltage and ultra-stable magnesium metal batteries

Magnesium metal batteries are considered as viable alternatives of lithium-ion batteries for their low cost and high capacity of magnesium.Nevertheless,the practical application of magnesium metal batteries is extremely challenging due to a lack of suitable electrolyte that can stabilize magnesium metal anode and high-voltage cathode simultaneously.Herein,we found that in-situ formed lithium/magnesium hybrid electrolyte interphases in conventional LiPF6-containing carbonate-based electrolyte can not only prevent the production of passivation layer on the magnesium metal anode,but also inhibit the oxidation of the electrolyte under high voltage.The symmetric magnesium‖magnesium battery can achieve reversible stripping/plating for 1600 and 600 h at 0.02 and 0.1 mA cm^(-2),respectively.In addition,when coupled with a carbon fiber cathode,the magnesium metal battery exhibited a capacity retention rate of 96.3% for 1000 cycles at a current density of 500 mA g^(-1)and presented a working voltage of ~3.1 V.This research paves a new and promising path to the commercialization process of rechargeable magnesium metal batteries.

Transient liquid phase bonding of TiC particulate reinforced magnesium metal matrix composite (TiC_p/AZ91D)

Microstructures and mechanical properties of transient liquid phase （TLP） bonded magnesium metal matrix composite （ MMC） joints using copper interlayer have been investigated. With an increase of bonding times from 5 min to 50 min at bonding temperature of 510 ℃ , the average concentration of copper in the bonded zone decreased, the microstructure in the zone changed from Cu, α-Mg and CuMg2 to α-Mg, CuMg2 and TiC, and mechanical properties of the joint increased. The shear strength of the joint bonded at 510 ℃ for 50 min reached 64 MPa due to the metallurgical bonding of the joint and improving its homogeneity of composition and microstructure. It is favorable to increase the bonding time for improving mechanical properties of TLP bonded magnesium MMC joint.

Synthesis and Crystal Structure of a Magnesium Metal-organic Framework

A magnesium metal organic framework, [N-H2（CH3）2][-N（CH3）4][Mgs（bpdc）3（O2CH）6]· 3H2O （1, bpdcH2 = 4,4＇-biphenyldicarboxylic acid）, has been solvothermally synthesized and structurally characterized. 1 crystallizes in the trigonal system, space group R-3, with a = 11.3427（3）, c = 41.5662（18） A, V = 4631.3（3） A^3, Z = 3 and the final R = 0.0457. Its structure features a pillared-layered three-dimensional network with 8.21 A cavities, in which cationic [NH2（CH3）2]^＋ or [N（CH3）4]^＋ and lattice water molecules are located. Thermal stability of the title compound has also been investigated.

Kinetic Factors for Intensive Reaction of Magnesium-Based Spheroidiser in Hot Metal

The spheroidiser is a necessary additive to manufacture ductile iron.Sometimes with the same hot metal,spheroidisers and treated technology,reactions differ greatly from each other.The reaction may be quite normal in one case,but very intensive for another one.The effects of kinetic factors such as size,surface area and morphology o f spheroidiser on the reaction of spheoidization are studied.

镁合金尾翼类构件径向同步加载工艺研究

目的针对常规挤压工艺成形尾翼类构件飞行时翼片径向产生挠曲变形的问题,提出了一种可调控金属流动的径向同步加载成形方法。方法结合ANSYS、Deform-3D有限元模拟和物理实验,分析径向同步加载的金属流动行为、等效应变和金属流线分布,通过拉伸实验测试成形翼片挤压方向(Extrusion Direction,ED)和横截面方向(Transverse Direction,TD)的力学性能,并通过观察显微组织揭示径向强化机理。结果径向同步加载通过对坯料施加周向压应力促进了金属径向流动,形成了沿径向分布良好的金属流线,有利于提升径向力学性能;采用该工艺试制构件表面质量良好,无宏观缺陷,且形成沿径向分布的宏观流线;翼片径向力学性能显著提升,屈服强度提升了57.8 MPa,抗拉强度提升了80.1 MPa,延伸率提升了1.4%,其强塑性的提升与纤维组织和块状LPSO相的纤维强化密切相关。结论实现了尾翼类构件的径向同步加载整体成形,通过调控金属流动形成径向分布良好的金属流线,提升了成形翼片径向强度,为高性能镁合金尾翼类构件的整体成形提供了理论基础和技术支撑。

半封闭空间内氢化镁粉尘爆炸火焰的传播特性

在自行搭建的5 L粉尘爆炸火焰传播特性实验装置中,实验研究了半封闭空间内氢化镁(MgH_(2))粉尘爆炸火焰的传播特性。实验结果表明:随MgH_(2)粉尘浓度的提高,MgH_(2)粉尘爆炸火焰由点火至稳定传播所用时间先缩短后延长以及预热区宽度先减小后增大,火焰亮度、锋面平滑度、及火焰传播速度呈先提高后降低的趋势,并在质量浓度为800 g/m^(3)时呈最佳燃烧状态。不同浓度的MgH_(2)粉尘爆炸火焰传播瞬时速度整体呈波动趋势,波动幅度随浓度的提高而先减小后增大,800 g/m^(3)时波动幅度最小,瞬时传播速度变化趋势随浓度的变化呈现不同的变化趋势。最后,根据MgH_(2)爆炸产物的XRD测试结果,分析MgH_(2)粉尘爆炸反应机理,发现MgH_(2)粉尘爆炸是以MgH_(2)燃烧反应为主并伴随有MgH_(2)和Mg(OH)2分解以及Mg和H_(2)氧化等多个总包反应的复杂过程,爆炸反应的最终产物为MgO。

Magnesium production by carbothermic reduction in vacuum

In present work,we investigate production of magnesium by carbothermic reduction under vacuum conditions.The process was divided into two parts,one is reduction process,and the other one is condensation process.The experimental results revealed that during reduction process,the gas-solid reaction between MgO and CO was not occurred at a temperature and pressure of 1723 K and 30-100 Pa respectively.So the main reduction reaction was MgO(_(s))+C(_(s))=Mg(_(g))+CO(_(g))(under vacuum)and reaction type belonged to solid-solid reaction.In Condensation Process,according to a contrast and analysis,the condensation quality of magnesium is associated with CO concentration.The resultant product C was formed and it followed magnesium vapor condensation which prevents mutual combination of two metal droplets to forms the compact condensation produces.Therefore,in order to compact morphological forms of magnesium crystal whiskers,we must control the technical conditions and find the method to separate the magnesium vapor and carbon monoxide.That's the key factor to get better crystalline structure.

金属离子抗炎作用的分子机制

背景:抵抗炎症反应是促进损伤组织修复的重要环节,改善医用生物植入材料所造成的局部炎症反应是近几年有待解决的关键问题。目的:综述常见金属离子的抗炎作用及相关分子机制,为改善生物植入材料导致的宿主早期炎症反应提供一定理论参考。方法:利用计算机检索PubMed、Web of Science、中国知网及万方数据库中相关文献,以“金属离子,镁离子,锌离子,银离子,铜离子,炎症,抗炎作用,氧化应激,免疫调节,信号通路”为中文检索词,以“metal ions,magnesium ion,zinc ion,silver ion,copper ion,inflammation,anti-inflammatory effects,oxidative stress,immunoregulation,signaling pathway”为英文检索词进行检索,通过阅读文题和摘要进行初步筛选,最终纳入80篇文献进行结果分析与总结。结果与结论:①镁、锌、银、铜等金属离子具有良好的抗炎作用,该抗炎作用的强弱与其剂量及作用时间具有强相关性,未来可考虑通过控制离子的释放速率以及调节适宜治疗浓度以达到最佳抗炎效果。②镁离子和锌离子表现出优异的抗炎活性,镁离子常以硫酸镁等化合物形式在抗炎治疗中发挥益处,锌离子则以锌饲料作为锌的主要补充来源调节机体炎症反应。③银离子和铜离子具有一定抗炎作用,但仍以优异的抗菌活性占首要地位,主要以纳米颗粒及生物涂层等方式发挥作用。④镁、锌等金属离子可与天然提取物结合形成复合物发挥抗炎作用,该方法具有价格低廉、来源广泛的优点,是可持续的绿色途径,值得临床推广。⑤镁、锌、银、铜等金属离子通过减少宿主氧化应激损伤、调节免疫细胞、抑制核转录因子κB、Toll样受体、STAT3和NOD等炎症信号通路共同发挥抗炎作用。⑥金属离子抗炎相关分子机制是一个复杂网络,并非是某个单一通路的作用,而应该是多个信号通路的集合,目前仍有许多潜在机制尚未被发掘,未来需要更加系统地阐明各个信号通路之间的相互联系。

生物活性离子改性透钙磷石骨水泥的生物和理化性能

背景:透钙磷石骨水泥作为一种骨替代和骨填充材料,因其具有良好的生物相容性、骨传导性等优点,尤其是相比于其他磷酸钙类骨水泥具有更好的生物降解能力,在骨修复方面有重要应用价值,但也因其存在机械性能不足、固化反应快及注射性能差等问题的限制,目前一般只能用于非负重区骨的修复。目的:探讨生物活性离子(金属离子和非金属离子)改性透钙磷石骨水泥,以期拓展使用范围。方法:利用Pub Med、Science Direct和中国知网、万方数据库检索2018-2023年发表的文献,中文检索词为“金属离子,铁,铜,锶,镁,锌,非金属离子,改性,骨,透钙磷石骨水泥”;英文检索词为“metal ion,iron,Fe,copper,Cu,strontium,Sr,magnesium,Mg,zinc,Zn,non-metal ion,modification,bone,Brushite Cements”。通过阅读标题、摘要对所得文献进行初筛,排除重复及内容不相关文献,最终纳入64篇文献进行综述。结果与结论:(1)生物活性离子影响透钙磷石骨水泥水化反应过程,不同离子以离子取代的方式掺入透钙磷石骨水泥晶体结构中,改变了骨水泥晶体形态,引起凝固时间、注射性、抗压强度等理化性能改变。(2)离子改性的透钙磷石骨水泥因不同的晶体结构而产生不同的离子释放效应,不同类型离子具有如促血管生成/成骨、抗菌及抗肿瘤等特性而发挥作用,此外,透钙磷石骨水泥具有良好的生物降解性,这对于各离子性能的发挥具有极大优势。(3)不同离子改性透钙磷石骨水泥理化性能影响如下:铁、铜、锶、镁、锌、银、钴可延长凝固时间;锶、镁可提高注射性能;铜、锶、镁、银、硅可增强抗压强度;能同时改善透钙磷石骨水泥以上3种理化性能的离子有锶、镁;良好的理化性能是临床应用的前提,故离子改善透钙磷石骨水泥的凝固时间、注射性及抗压强度等性能对骨水泥的研究应用具有重要意义。(4)不同离子改性透钙磷石骨水泥生物性能影响如下:铜、锶、镁、锌、钴、锂、硅、硒具有促血管生成/成骨效应;铁、铜、镁、锌、银具有抗菌特性;镁离子具有抗炎特性;铜、硒具有抗肿瘤性。(5)综上所述,镁离子能改善透钙磷石骨水泥凝固时间、注射性和抗压强度,同时具有促新生血管生成/成骨及抗菌性,对合并感染的骨缺损治疗具有良好应用前景;此外,铜还具有抗肿瘤特性,因此铜离子在感染、肿瘤引起的骨缺损治疗方面有巨大潜力;只是目前相关研究仍处于基础研究阶段,不同离子掺杂浓度和合成条件等对透钙磷石骨水泥理化性能的影响需进一步探索,同时对于生物性能影响也需更长期的研究观察。

金属离子促血管生成机制及在骨组织工程中的应用

背景:多种金属离子因具有良好的血管生成活性,并参与成骨中血管新生等生理过程,在骨组织工程领域的研究和应用正日益深入。目的:系统性阐释铜(Cu2+)、镁(Mg2+)、锶(Sr2+)、锌(Zn2+)、钴(Co2+)离子的促血管生成机制及其在骨组织工程的应用现状和主要治疗的疾病类型。方法:2位作者利用Pub Med和中国知网数据库检索2017-2022年间发表的文献,中文检索词为“铜离子,镁离子,锶离子,锌离子,钴离子,骨,血管生成”;英文检索词为“copper,cuprum,Cu,magnesium,Mg,strontium,Sr,zinc,Zn,cobalt,Co,metal ion,angiogenesis,bone”。通过阅读标题、摘要对所得文献进行初筛,排除不相关文献后,最终纳入114篇文献进行综述。结果与结论:(1)金属离子可以通过作用于血管内皮生长因子、缺氧诱导因子、血管生成相关基因、内皮细胞以及对巨噬细胞进行免疫调节等途径调控血管生成。(2)铜、镁、锶、锌、钴等金属离子因具有显著的血管生成效应,常用于组织工程支架的性能改善,其中水凝胶、生物陶瓷和合成聚合物材料目前应用较为广泛,镁及其合金也因其优良的承重能力颇具优势,但这些材料均存在一些缺陷,目前暂时没有一种理想的骨替代材料。(3)不同的离子作用特点如下:铜具有抗菌、成血管和成骨等性能,主要用于感染及肿瘤等引起的骨缺损;镁、锌具有较强的生物降解性,需要对降解速率进行控制;镁具有腐蚀性,主要以合金形式应用;锌的成血管机制涉及较少;镁、锶用于治疗骨质疏松性骨缺损效果显著。(4)以上5种金属离子(铜、镁、锶、锌、钴)具有显著的促血管生成作用,也通过成血管来促进成骨,个别离子如铜离子具有杀菌作用,这些金属离子可以作为治疗肿瘤、骨质疏松症、感染和创伤等引起的骨缺损的新策略,但是目前的临床试验和产品的应用性研究相对不足。

燃煤锅炉烟气湿法脱硫废水中重金属及钙镁离子沉淀规律研究

燃煤锅炉烟气湿法脱硫废水中的重金属及钙镁等离子危害较大,开展其沉淀去除规律的研究有利于废水中有用元素的资源化回收和废水的回用。采用碱液沉淀法对脱硫废水进行分级处理,对沉淀产物采用SEM-EDS等手段进行表征。结果表明,采用氢氧化钙作为沉淀剂可以实现去除重金属、回收镁资源及去除氟化物和降低废水硬度等多种目标。在去除重金属离子的过程中,当脱硫废水pH值为9.0~9.5时,废水中的重金属离子可得到有效去除且达到污水排放标准,镁离子几乎没有损失,钙增加率也较低,仅为4.6%以下;将废水pH值调整为9.5~9.7可有效回收废水中的镁元素,镁的回收率在62%以上,回收效果较好。在碱性条件下,向废水中投加Na_(2)CO_(3)可有效降低废水中的钙离子和残留的镁离子,实现废水降硬的目标。不同pH值下沉淀物的SEM-EDS能谱显示,对脱硫废水进行梯级pH处理可以达到分级去除重金属污染物和回收镁元素的目标。通过对脱硫废水中重金属及钙镁结垢离子的沉淀规律研究,实现了废水的分质分盐有用成分的资源化回用,避免了产生杂盐危废造成二次污染的可能,达到了脱硫废水的零排放的目标。

钙锶镁锌交联藻酸盐水凝胶的制备及其细胞相容性研究

目的:制备4组含不同种类二价金属离子Ca^(2+)、Sr^(2+)、Mg^(2+)、Zn^(2+)交联的藻酸盐凝胶支架,检测其理化性能,观察MC3T3-E1细胞在各组凝胶表面的黏附、增殖及成骨分化情况。方法:配制4组离子总浓度为6.5g/L且含不同种类Ca^(2+)、Sr^(2+)、Mg^(2+)、Zn^(2+)的混合溶液作为交联剂,与海藻酸钠溶液发生螯合反应制备多离子交联水凝胶,依据所含离子种类分为Ca组、Ca-Sr组、Ca-Sr-Mg组、Ca-Sr-Mg-Zn组,Ca组为对照组。使用扫描电镜观察凝胶冻干后的表面形态,检测其降解、溶胀性能及Sr^(2+)、Mg^(2+)、Zn^(2+)析出浓度。将MC3T3-E1细胞接种在水凝胶表面,观察细胞黏附形态,采用CCK-8法和活死染色法评价其生物安全性和细胞增殖能力。诱导MC3T3-E1细胞成骨分化,检测ALP活性,茜素红染色观察钙盐沉积情况,RT-qPCR检测成骨基因的表达。结果:与Ca组相比,Ca-Sr组、Ca-Sr-Mg组、Ca-Sr-Mg-Zn组水凝胶的孔隙更均匀致密,凝胶的降解速度与溶胀率均减小(P<0.05),细胞在凝胶表面的黏附形态由球形变为多角形;与Ca组比较,Ca-Sr组、Ca-Sr-Mg组、Ca-Sr-Mg-Zn组水凝胶表面的细胞增殖活性、细胞内ALP活性、钙结节生成面积及I型胶原、骨形态发生蛋白2、Runt相关转录因子2等成骨基因的表达量升高(P<0.05),且Ca-Sr组、Ca-Sr-Mg组、Ca-Sr-Mg-Zn组水凝胶表面的细胞增殖活力及成骨分化效果依次提高(P<0.05)。结论:较Ca^(2+)交联的海藻酸钙水凝胶相比,使用Ca^(2+)、Sr^(2+)、Mg^(2+)、Zn^(2+)混合金属阳离子作为交联剂,能改善藻酸盐水凝胶的理化性能,促进MC3T3-E1细胞在凝胶表面的黏附及成骨分化。

气力输送系统在无水氯化镁颗粒输送上的应用

无水氯化镁原料具有易吸水性和强度差的特性,选择一种合适的输送方式成为关键。气力输送系统是通过消耗气流的一定动能,将物料在封闭的管道内沿着一定方向向前推送的过程,它具有输送管路完全密闭、输送物料不会被外界物质污染、输送管路布置灵活、占用空间较小、自动化程度高的特点。利用干燥过后的压缩空气作为输送气源,以低速的浓相气力输送无水氯化镁,不仅可阻断外界空气与无水氯化镁接触,防止空气中的水分污染无水氯化镁,输送时物料速度低,不易破碎,而且效率和自动化程度高,可大幅降低生产人工成本。

TiO_(2)直接还原制备超低氧钛

提出在MgCl_(2)−KCl−YCl_(3)熔盐中,通过熔盐电解产生Mg直接还原TiO_(2)制备低氧钛。绘制Mg−Ti−O三元相图和电位−氧势(φ−pO^(2)−)图,表明镁还原TiO_(2)制备低氧钛是可行的。在MgCl_(2)−YCl_(3)和MgCl_(2)−YCl_(3)−KCl熔盐中,不同温度和施加电压条件下,开展熔盐电解−镁热还原TiO_(2)实验研究,结果表明:借助YOCl沉淀及CO_(x)同步生成,将还原和脱氧产物O^(2)−快速脱除,在1073~1173 K、施加电压2.5~3.1 V的条件下,通过电化学还原可以将TiO_(2)还原为高氧钛(Ti6O)。在温度为1173 K的MgCl_(2)−YCl_(3)熔盐中,开展不同施加电压下的高氧钛电化学脱氧实验。此外,还观察到有可能将高氧钛的氧含量可从1200×10^(−6)降至100×10^(−6)以下。

镁合金表面介孔SiO_(2)改性等离子体电解氧化复合涂层组织与性能研究

为了在镁合金表面制备对损伤具有自修复能力的复合涂层,本文将负载了缓蚀剂8-羟基喹啉(8-HQ)的介孔SiO_(2)微容器掺杂在环氧树脂涂层中,并涂敷在经等离子电解氧化处理的镁合金AZ91D试样表面,制备了介孔SiO_(2)改性的等离子体电解氧化复合涂层。采用TEM、FT-IR、UV及TGA研究了8-HQ在微容器中的负载及释放规律;通过SEM、电化学测试研究了改性后的复合涂层表面微观形貌、耐蚀性、自修复效果及其自修复机理。研究结果表明:8-HQ在介孔SiO_(2)内的最大负载率约为16%,并在40 min内基本释放完全;通过预制缺陷,证明了涂层具备自修复能力,且自修复效率约为93%;改性后的复合涂层表现出更好的耐蚀性,从而提高了镁合金在实际应用中的使用寿命。

基于内非金属元素掺杂的外微波电场协同增强镁储氢机理研究

在众多的固态储氢材料中,镁基材料已被公认为极具应用前景,但镁在储氢过程中需要克服动力学性能差(氢解离扩散难)、反应能耗高等难题,因而阻碍了其大规模商业化应用。微波外场可高效加速化学反应并降低反应温度和能耗,已逐渐应用于改善储氢过程,但目前针对内非金属元素掺杂外微波电场协同增强镁储氢的研究鲜有报道。为此,基于第一性原理计算探究了内掺杂非金属元素外微波电场协同改善镁储氢的作用机制,分析了有无非金属元素掺杂下镁—氢气体系在微波电场作用前后的吸附能、电子特性、过渡态等热动力学性能变化机理。研究结果表明:①微波电场改变了氢气分子和镁表面的电荷分布,使得氢气分子出现电荷分离(发生极化);②态密度计算结果也表明微波电场改变了H-s轨道的电子态分布,使得H-s电子向高能量区域移动,从而增强H-s与Mg-sp轨道杂化,导致镁与氢气之间的相互作用增强;③内非金属元素掺杂外微波电场协同改性使吸氢过程的反应能垒从0.94 eV大幅降至0.77 eV。结论认为:①微波电场有助于氢气发生极化,激活了氢气的反应活性,降低反应能耗;②内非金属元素掺杂外微波电场协同改性促进了氢气在镁表面的反应进程,有效提高了镁吸氢过程的动力学性能。

取向硅钢表面点状露金成因研究

对取向硅钢表面的点状露金缺陷的形成原因进行了模拟和研究,采用金相显微镜观察缺陷表面形貌,再采用扫描电镜的面扫描功能分析缺陷成分分布。研究结果表明:取向硅钢在夏季及秋季生产时,因为降雨量多且气温高,空气湿度大,空气中的水蒸气会冷凝在硅钢卷上,硅钢卷表面氧化镁的含水率升高,在水和氧气的作用下,硅钢基体表面产生很多氧化腐蚀点。这些氧化腐蚀点会阻碍高温退火过程中硅酸镁底层的形成,并且在温度升高后与罩室炉内的氢气反应,氧化产物被还原,经酸洗后,最终成品表面留下圆形的白色露金。