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Reduction of the substitutional disorder by heat treatments in Mn2-xCoxVAl Heusler alloys 热处理降低Mn2-xCoxVAl Heusler合金中的取代无序
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-25
D. Benea, R. Gavrea, M. Coldea, L. Barbu-Tudoran, O. Isnard, V. Pop
We report on the preparation and the atomic disorder reduction by annealing in Mn2xCoxVAl Heusler alloys. The degrees of the B2 and L21 atomic ordering for the as-cast samples, obtained from intensity ratios of (200) and (111) peaks respectively related to (220) peak of the Xray patterns, are significantly improved after annealing at 700 800 °C for 72 h. The diminution of the substitutional disorder is essential in these types of compounds, as the half-metallic character and the magnetic properties are primarily influenced by this factor. Introduction Heusler alloys are ternary intermetallic compounds of the L21 structure with stoichiometric composition X2YZ, where X and Y are usually two different transition metals and Z is a nonmagnetic element [1]. Earlier studies have shown that Mn2VAl Heusler alloy is a half-metallic ferrimagnet [2-5]. This compound is characterized by an antiparallel coupling between the Mn and V magnetic moments, the total spin moment being 2 μB per formula unit [2, 3]. The high Curie temperature of 760 K [3] makes it interesting for spintronic applications. The spin compensation in Mn2−xCoxVAl alloy was induced by progressive substitution of Co for Mn and a fully compensated ferrimagnetic behavior has been experimentally obtained for the MnCoVAl alloy [4]. The presence of a considerable atomic disorder in the Mn2VAl compound due to the intermixing of the V and Al atoms has been reported [5]. Previous studies have shown that the magnetic properties and the half-metallic character of these Heusler alloys are strongly influenced by the crystallographic disorder [1, 3, 6, 7]. The aim of the present work is to reduce the substitutional disorder by heat treatments in Mn2−xCoxVAl Heusler alloys. For the evaluation of the atomic ordering in the full Heusler alloys, the Takamura’s model has been used [8]. In order to determine and to adjust the ordering parameters defined in this model, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and neutron diffraction studies have been performed. Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 219-227 doi: http://dx.doi.org/10.21741/9781945291999-25 220 Experimental details The Mn2−xCoxVAl (x= 0, 0.2, 0.6, 1) ingots were prepared by induction melting under a purified Ar atmosphere of the starting components Mn (99.95 wt %), Al (99.999 wt %), V (99.99 wt %) and Co (99.99 wt %). An excess of 3 wt % of manganese was added to the stoichiometric mixture in order to compensate for preferential Mn evaporation during the melting processes. The samples were turned and remelted repeatedly in order to ensure homogeneity. The water-cooled copper crucible ensured a rapid cooling of the alloys after melting. The samples were wrapped in tantalum foil, sealed in quartz tubes and subsequently annealed in an Ar atmosphere for 72 hours. The stoichiometry of our as-cast samples was investigated using the energy dispers
Heusler合金的X2YZ - l21型晶体结构。图3所示。铸态Mn2-xCoxVAl样品的室温x射线衍射图。数据被归一化为(220)反射的强度。粉末冶金与先进材料- RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 211 -227 doi: http://dx.doi.org/10.21741/9781945291999-25 222铸态Mn2−xCoxVAl (x = 0,0.2, 0.6和1)合金的室温x射线衍射图如图3所示。XRD分析结果表明,铸态合金为单相结晶,属于X2YZ Heusler型结构,立方空间群Fm3 μ m(空间群no.;225),其中Mn和Co原子占据8c Wyckoff位(X),而V和Al原子分别位于4a (Y)和4b (Z)晶体位(见图2)。XRD谱图的(111)和(200)超晶格衍射线证明,Mn2-xCoxVAl合金均表现出完整Heusler合金的稳定L21结构。从(111)面反射的消光表明V原子和Al原子之间的混合。同样,如果所有Mn、V和Al原子混合,则超晶格反射(111)和(200)都将消失[1,4,8]。我们采用Takamura的模型来研究我们的Mn2−xCoxVAl (x = 0,0.2, 0.6和1)合金中的取代无序。在该模型中,定义了两种排序参数来描述原子位置之间的混合。SB2阶参数描述了Mn原子在X2YZ全Heusler合金中占据X位(8c)的概率,定义为:SB2 = MMM oM X - MMM oM X rrMror MMM oM X ffff - MMM oM X rrMror(1);二级参数SL21描述了V原子在X2YZ全Heusler合金中占据Y位的概率:SL21 = MVoM Y - MVoM Y rrMror MVoM Y ffff - MVoM Y rrMror(2)。铸态Mn2−xCoxVAl样品的结构参数包括SB2和SL21排序参数、单元常数和位点占用。Co含量(x)原子数x位Y位Z位SB2 SL21 alat (nm)
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引用次数: 1
Synthesis and characterization of various surfactants for stabilized CuO powder 稳定型氧化铜粉体表面活性剂的合成与表征
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-6
B. Bita, V. Ţucureanu, I. Cernica, M. Popescu, A. Matei, C. Romanițan
In the present work, CuO nanoparticles were successfully prepared by the coprecipitation method using copper acetate (Cu(CH3COO)2) as a basic precursor, sodium hydroxide (NaOH) as a precipitator material, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) as anionic and cationic surfactants, respectively. The synthesized powders samples were characterized by Fourier transform infrared spectrometry (FTIR), field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The investigation showed that the added types of surfactants have effects on the decrease of the crystallite size, on the CuO particles morphology, shape and uniform distribution as it is noticed in the XRD and SEM characterizations. Additionally, the FTIR spectra for all the powders samples showed the same Cu-O stretching vibration mode which indicates the presence of a crystalline CuO monoclinic structure. The obtained results create premises for further advanced the applications of CuO powders in various domains. Introduction Over the years, the interests in developing nanoparticles metal oxides have considerably increased due to the necessity of obtaining materials with outstanding physical and chemical properties. Various methods of metal oxide synthesis have been know so far, researches continue to development a new approaches with a strict control over nanoparticles morphology, size and composition for several technological applications. Copper oxide (CuO), belonging to the nanomaterials class, which has attracted recent research because of its excellent properties, cost effectiveness and wide spectrum of practical applications (solar and electrochemical cells, gas sensors, field emitters, active catalyst and antimicrobial activity, etc.). Also, CuO as nanostructured oxide being classified as a p-type monoclinically structured semiconductor material with a direct band-gap value of 1.85 eV presents a particular attention. This type of material has a special concern because it extends the use in a board range of applications, such as electronics and optoelectronics, catalysts, sensors and biosensors, chemical sensing devices, nanofluids and field emitters, desinfection, cosmetic pigments, antibacterial agent, etc. [1–4]. In order for this material to exhibit viable properties in the desired field of applicability, it is intended to establish its method of obtaining and its synthesis parameters; there Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 52-60 doi: http://dx.doi.org/10.21741/9781945291999-6 53 have been elaborated and known various physical and chemical methods so far, such as sol-gel, coprecipitation, hydrothermal synthesis, mechanical mixing, solid state reaction, thermal descomposition of precursors, microemulsion, microwave irraditiaon, physical vapor deposition, ablation, etc. [3, 5, 6]. From the bottom-up type methods, precipitation is a cheap one, w
本文以乙酸铜(Cu(CH3COO)2)为碱性前驱体,氢氧化钠(NaOH)为沉淀剂,十二烷基硫酸钠(SDS)和十六烷基三甲基溴化铵(CTAB)分别为阴离子和阳离子表面活性剂,采用共沉淀法成功制备了CuO纳米颗粒。采用傅里叶变换红外光谱(FTIR)、场发射扫描电镜(FESEM)和x射线衍射(XRD)对合成的粉末样品进行了表征。XRD和SEM表征表明,表面活性剂的添加类型对CuO颗粒的形貌、形状和均匀分布都有影响。此外,所有粉末样品的FTIR光谱显示出相同的Cu-O拉伸振动模式,表明存在结晶CuO单斜结构。所得结果为进一步推进氧化铜粉体在各个领域的应用创造了前提。多年来,由于需要获得具有优异物理和化学性能的材料,人们对纳米金属氧化物的开发兴趣大大增加。金属氧化物的合成方法多种多样,研究人员不断开发新的方法,严格控制纳米颗粒的形态、大小和组成,用于多种技术应用。氧化铜(CuO),属于纳米材料类,因其优异的性能、成本效益和广泛的实际应用(太阳能和电化学电池、气体传感器、场发射体、活性催化剂和抗菌活性等)而受到近年来的研究。此外,CuO作为纳米结构氧化物被归类为p型单临床结构半导体材料,其直接带隙值为1.85 eV,引起了特别的关注。这类材料受到特别关注,因为它扩展了电路板的应用范围,如电子和光电子、催化剂、传感器和生物传感器、化学传感装置、纳米流体和场发射器、消炎、化妆品颜料、抗菌剂等[1-4]。为了使该材料在期望的应用领域中表现出可行的性能,拟建立其获得方法及其合成参数;粉末冶金与先进材料- RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 52-60 doi: http://dx.doi.org/10.21741/9781945291999-6 53迄今为止已经阐述和了解了各种物理和化学方法,如溶胶-凝胶,共沉淀,水热合成,机械混合,固相反应,前驱体热分解,微乳液,微波辐照,物理气相沉积,烧蚀等[3,5,6]。从自下而上的方法来看,沉淀法成本低,适用范围广,且不需要添加二次反应产物[7-9]。特别是,为了获得CuO,该方法涉及在水溶液中沉淀各种可溶性铜盐(硝酸盐、氯化物、硫酸盐和醋酸盐),然后热分解生成氧化物[4,5,10]。将无机盐用NaOH、KOH、(NH4)2CO3或NH4OH溶液在严格的pH控制下,在水介质中混合,最后得到沉淀,进行特征热处理。在合成过程中,反应参数(pH、反应物的加入速度、搅拌速度、溶液浓度、反应温度等)对颗粒的大小、形貌和粒度具有决定性作用[11 - 13]。文献中提出了在相对高温(700 ~ 1100℃)下的各种热处理方法,导致颗粒团聚现象,颗粒平均尺寸增大。为了防止团聚的倾向,有利于纳米结构材料的形成,建议使用表面活性剂。由于静电和硬脂稳定机制降低了溶液的表面张力,改善了纳米晶材料的性能,不同表面活性剂的使用可以改善颗粒的结构、物理化学和形态性能[6,14 - 18]。此外,在氧化材料沉淀过程中加入表面活性剂可以提高纳米颗粒的稳定性以及表面活性剂分子与金属离子之间的相互作用。表面活性剂是一种化学物质,主要作用于相对亲和力较低的表面和可溶解物质。它们具有不对称的分子结构,由非极性(碳氢化合物)和极性(可电离或不可电离)部分组成。 表面活性剂的作用是提供一种有效的涂层,以诱导静电或硬脂排斥,从而抵消范德华引力[19 - 22]。专业文献显示,利用油酸(OA)、聚乙二醇(PEG)、十六烷基三甲基溴化铵(CTAB)、次氯酸十二烷基硫酸酯(SDS)、聚乙烯吡咯烷酮(PVP)、四辛基溴化铵(TOAB)等不同类型的表面活性剂来改善纳米CuO的性能和形成的研究,从初始阶段起就在合成过程中起着重要作用。本研究实验中选择CTAB和SDS两种表面活性剂的原因是基于它们对颗粒稳定性、粒径变化、形貌和沉淀颗粒表面性能的显著影响,同时也因为它们价格低廉,在市场上相对容易找到,毒性低[7,14,23 - 25]。本文研究了在阴离子(SDS)和阳离子(CTAB)两种表面活性剂存在和不存在的情况下,用共沉淀法制备CuO纳米颗粒。研究了表面活性剂对纳米CuO形貌、平均尺寸和晶体结构的影响。利用场发射扫描电镜(FESEM)、x射线衍射(XRD)和傅里叶变换红外光谱(FT-IR)对其形貌和结构进行了表征。粉末冶金与先进材料- RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 52-60 doi: http://dx.doi.org/10.21741/9781945291999-6 54实验细节:以一水乙酸铜[Cu(CH3COO)2]、氢氧化钠[NaOH]和阴离子型表面活性剂[C12H25NaO4S, SDS 99%]和[C19H42BrN, CTAB > 99%]为原料合成CuO粉末。所有试剂均购自Sigma-Aldrich公司,未经任何纯化。为了在无表面活性剂和有表面活性剂的情况下合成CuO,分别制备了1M [Cu(CH3COO)2]和1M [NaOH]的原液。从乙酸原液中取一部分,在碱性介质中,通过滴加NaOH溶液调节pH,直至观察到形成青蓝色沉淀。在有表面活性剂的样品中,在铜源上加入进样表面活性剂(SDS和CTAB浓度为0.1 M),在连续搅拌的情况下,滴入沉淀剂(NaOH),直至沉淀形成,并将pH调至1011左右。沉淀形成后,继续搅拌至80℃。引入SDS阴离子表面活性剂后,由于反离子在晶面上的尺寸效应,导致了均匀的核过程。通过添加CTAB作为阳离子表面活性剂,在四面体结构中实现了完全的电离和阳离子形成,但也决定了CuO纳米颗粒不同面生长速率的控制[14,26]。所有合成样品均保持相同的合成条件(时间、温度和pH)。这样形成的沉淀物被留在剩余位置,然后用布克纳漏斗在真空下过滤,然后用水-乙醇混合物洗涤,以净化和去除二级化合物。样品洗净后,在80℃的烘箱中烘干,然后在550℃的常压下煅烧烧结3小时。由于干燥样品的烧结温度,颜色由绿色变为蓝色再变为黑色。采用傅里叶变换红外光谱法(Bruker Optics, Vertex 80V)对合成的氧化物样品的官能团和化学键进行了分析,平均扫描64次,波数范围为4000 ~ 400 cm。在所有光谱的处理中,提取了CO2中C=O键的振动模式的能带。为了研究其形貌和颗粒大小,使用了在10 kV工作电压和30 000x量级下获得的场发射扫描电子显微镜(FE-SEM)。合成的CuO粒子的x射线衍射测量使用Rigaku Smartlab衍射仪记录,辐射CuKa=1.540593 Å,表明电流的变化极限在150 mA到190 mA之间。以12°/min的扫描速率收集数据。在20 = 20-95°范围内。不同样品的FTIR光谱是在没有表面活性剂(图1a)和有表面活性剂(图1b和c)的情况下获得的CuO粉末的比较。
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引用次数: 1
A comparative study of the Co-based amorphous alloy prepared by mechanical alloying and rapid quenching 机械合金化与快速淬火法制备co基非晶合金的比较研究
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-18
B. Neamțu, T. Marinca, H. Chicinaş, F. Popa, I. Chicinaș, O. Isnard, G. Ababei, M. Gabor
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引用次数: 0
Green synthesis of Reduced Graphene Oxide (RGNO) / Polyvinylchloride (PVC) composites and their structural characterization 还原氧化石墨烯(RGNO) /聚氯乙烯(PVC)复合材料的绿色合成及其结构表征
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-16
F. Mindivan, M. Goktas
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引用次数: 3
Composite material obtained by powder metallurgy with applications in the automotive industry 粉末冶金获得的复合材料在汽车工业中的应用
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-23
C. Pascu, Ș. Gheorghe, C. Nicolicescu, D. Tărâţă
Because of their great properties titanium and titanium alloys have been used in automotive industry, biomedical applications, aerospace industry, computer components, emerging applications, architecture of buildings, etc. In the last decade there has been revived interest in the utilization of the Powder Metallurgy (PM) route as a low-cost way for obtaining components from this alloys. This research presents the experimental results concerning the processing of Ti based alloy by Two-Steps Sintering and Multiple-Steps Sintering, techniques belonging to PM technology. The initial powder mixture consists in TiH2 powder particles that have been combined with some metallic powders (Al, Mn, Sn, Zr) for improving the final mechanic-chemicals and functional properties for using in the automotive industry. As a result it was studied the physical-mechanical properties after sintering, the influence of the sintering temperature and time on the microstructural changes of the composite material based on titanium. Introduction Titanium alloys have multiple applications in diverse fields such as industrial and medical fields [1-4]. This is due to their excellent performances such as: low density, good corrosion resistance, non-magnetic properties, high specific strength, high chemical stability, resistant to high temperatures, etc. [5, 6]. The basic advantages of titanium alloys in terms of the automotive industry are the high strength to density, their low density, the outstanding corrosion resistance [7, 8]. In the automotive field, one of the greatest applications of titanium-based materials is for components of the internal combustion engine area that equip the vehicle (pistons, valves, connecting rod, crank caps, bolts, etc.) [9, 10]. Also, for modern jet turbine engines titanium alloys usually represent approximately 30% of the used materials, especially in the forward zone of the engine [11]. However, compared to other traditional materials, the major impediment represents the high cost of titanium [12]. Another disadvantage of titanium for applications in the automotive industry is its low tribological properties because of poor plastic shearing resistance and work hardening ability [13, 14]. Using inexpensive alloying elements (such as Sn, Mn, Fe, Cr, etc.) instead of expensive alloying metals (V, Nb, Mo, Zr, etc.) to improve the strengthen alloys is one of the methods to reduce the cost of manufacturing titanium alloys [15]. Due to the properties they possess, by alloying Ti with small amounts of aluminium percentage a Ti-Al (γ Ti-Al) alloy is obtained with excellent mechanical properties and corrosion resistance at Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 200-211 doi: http://dx.doi.org/10.21741/9781945291999-23 201 temperatures above 700°C, which allows the replacement for traditional Ni based superalloy for turbine engine components [16]. Due to the very good wear b
在PM方法中,似乎提供了最大的机会来降低实际成本,人们认为两步(TSS)和多步(MSS)烧结技术允许获得不同成分和显微结构的Ti产品用于汽车零部件[27]。传统的获得钛合金的方法需要特殊的可控气氛条件,这导致获得这些合金的成本很高[28]。因此,在过去的十年中,许多研究都集中在使用TiH2粉末进行粉末冶金制备ti合金[29-34]。根据[35],用氢化钛粉末进行粉末冶金制备了Ti-6Al-2Sn-4Zr-2Mo合金。以TiH2粉末为基体制备的合金具有较好的力学性能和较高的耐高温腐蚀性能。本研究提出通过添加少量Al、Sn、Mn、Zr和C来改善该合金的力学和摩擦学性能,并采用TSS和MSS技术,通过压实和烧结来实现进一步的加工。本研究采用Chemetall公司生产的氢化钛(TiH2)作为初始材料。TiH2成分中存在以下化学元素:钛(最小95%),氢(最小3.8%),Al(最大0.15%),Si(最大015%),氮(最大0.3%),Fe, Ni, Cl, Mg, C, Ni(最后一个成分都在0.1%以下)。为了改善初始粉末的机械和摩擦学特性,通过混合60分钟引入以下粉末冶金和先进材料- RoPM&AM 2017材料研究论坛LLC材料研究进展8 (2018)200-211 doi: http://dx.doi.org/10.21741/9781945291999-23 202成分:Mn粉末,Sn粉末,Alumix 321, 8%粉末,Zr粉末和石墨粉末。混合料的混合和均质在Fritsch公司的经典球磨机中进行,球:粉比1:1,250 ml研磨碗,氩气,球材料不锈钢- 1.3541 ISO/EN/DIN codeX47Cr14, B50,主盘转速200转/分。各组分之间的重量比为:80%wt。wt TiH2, 8%。, Mn, 3%wt。锡、wt 2%。锆、wt 6%。Alumix321,和1%wt。C.粒径分布如图1所示,采用动态激光散射(DLS)技术,采用美国布鲁克海文仪器公司的90Plus粒径分析仪,配备35mw固体激光器,波长为660 nm。温度为25℃,散射角为90°。将粉末在水中稀释,并对溶液进行超声波处理5分钟,以避免颗粒絮凝。图1所示。混合料的粒度分布。图2所示。混合物的SEM图像。图2显示了混合物的SEM图像。混合物的粒径呈双峰分布,粒径分别在(188 ~ 294 nm) (1110 ~ 1730 nm)之间。最高数量的粒子(占总数的28%)的尺寸等于225纳米。粒径较大的颗粒所占比例小于1.5%。平均水动力直径为291 nm。表1给出了与图1所示粒度分布相对应的亚微米尺寸和粉末颗粒百分比。方法与技术将均匀化后的混合料在600MPa压实压力下单侧冷压实,制成直径为12.05 mm的圆柱形试样。采用一台100 kN的A009机电微机试验机,安装TCSoft2004Plus软件进行单侧冷压试验。每个部分的绿色密度已根据先前的研究[27]确定。下一步是绿色粉饼的烧结。他们使用粉末冶金技术使用了四种不同的烧结制度如下:V1制度,在1050°C下使用经典烧结,停留时间为90分钟;两步烧结(TSS)制度,V2,在1050℃下停留时间为15分钟,然后在1000℃下停留75分钟;TSS状态,V3,在1050°C下烧结15分钟,在950°C下烧结75分钟,图3;粉末冶金和先进材料- RoPM&AM 2017材料研究论坛有限责任公司材料研究进展8 (2018)200-211 doi: http://dx.doi.org/10.21741/9781945291999-23 203多步烧结(MSS), V4,在1050°C, 15分钟的停留时间,1000°C, 20分钟的停留时间和900°C, 55分钟的停留时间,图4。表1。粒度分布及粉末颗粒百分比尺寸[nm]粒度分布[%]189 11.8% 206 23.6% 225 28% 246 19.6% 269 9.2% 294 1.9% 1110 1.1% 1213 0.8% 1326 2% 1448 1.4% 1583 0.3% 1729 0.3%TSS循环为1050°C和950°C。图4所示。MSS循环在1050 /1000/ 900°C。
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引用次数: 1
A study of the ferromagnetic microwires retention in cellulose matrix in the security papers 防伪纸中纤维素基质中铁磁微丝的保留研究
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-1
I. Zapodeanu, M. Codescu, M. Burlacu, V. Midoni, R. Erdei, D. Pătroi, E. Patroi, E. Manta, K. Kappel
Prepared by the Taylor – Ulitovsky technique, the glass-coated microwires are formed from a metallic core, with the diameter 3 to 50 μm, surrounded by an insulating layer from glass, with the thickness of 1 to 20 μm. Embedded in the cellulose matrix, the ferromagnetic glasscoated microwires allow their use as security element for the authentication of valuable papers in the electronic validation process. The authentication of the security paper is realised with a special detector, by “YES” or “NO” answer. This paper can be used as anti-shoplifting or validating elements to identify the counterfeit products. The paper presents the experimental results related to the retention of ferromagnetic microwires in the cellulose matrix, a complex process characterised by specific features, primarily due to the shape and diameter/length ratio of the microwires. The ferromagnetic retention yield was η = 65 – 90%, for the prepared papers with basis weight more than 50 g/m. Introduction Faced with increasing of goods counterfeiting, a wide range of methods are currently used to protect consumer goods, bank, state and commercial documents. Thanks to impossibility to produce security elements without proper equipment and under special conditions imposed by the very high degree of accuracy, the advanced technologies offer the solution, ensuring a high degree of protection against falsification. Investment and research efforts are being made to diversify the field of high security elements. The moment of launching the technology for glass-coated microwires (GMW) fabrication [1,2] has become revolutionary on the high-tech technology market, opening up the gates of a large variety of technological benefits for the existing applications and also setting the foundation for new applications [3-9]. The advantages of ferromagnetic GMWs securing [10] were: possibility of identifying at distance; stable magnetic properties even at high temperatures and corrosive media; wide range of functional temperatures; stability at shielding – the codes shielded by metallic panels can be read; stability at the mechanical action; small sizes and low consumption and, for the microfibbers from the last generation, with special properties, allowing the possibility to the information magnetic encoding): very large amount of the generated codes; the information can be read both from a stationary source and from a source in motion; the encoding is impossible to destroy, both in the Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 1-10 doi: http://dx.doi.org/10.21741/9781945291999-1 2 continuously and in variable magnetic field, (reliable encoding); possibility to read the information from any code randomly oriented in space. The structure of the paper consists of vegetable fibers (wood or non-wood), in which auxiliary materials, such as fillers, gluing agents, pigments, additives etc. are incorporated. Depending on t
由泰勒- Ulitovsky技术,金属的玻璃微丝形成核心,直径3 - 50μm,从玻璃绝缘层包围,1到20μm的厚度。嵌入在纤维素基质中,铁磁玻璃涂层微线允许它们作为电子验证过程中有价值文件认证的安全元素。通过“是”或“否”的回答,通过一个特殊的检测器来实现安全纸的认证。本文可以作为防入店行窃或识别假冒产品的验证元素。本文介绍了与铁磁微丝在纤维素基质中的保留有关的实验结果,这是一个具有特定特征的复杂过程,主要是由于微丝的形状和直径/长度比。铁磁潴留率η= 65 - 90%,准备论文的基础重量超过50 g / m。面对越来越多的商品假冒,目前使用了各种各样的方法来保护消费品,银行,国家和商业文件。由于不可能产生安全元素没有适当的设备和在特殊的条件下实施的精确度很高,先进技术提供解决方案,确保高度的防范伪造。投资和研究正在努力多样化高安全领域的元素。玻璃涂层微线(GMW)制造技术的推出[1,2]已经成为高科技技术市场上的革命性技术,为现有应用打开了各种技术效益的大门,也为新的应用奠定了基础[3-9]。铁磁gmw固定[10]的优点是:可以远距离识别;稳定的磁性甚至在高温和腐蚀性介质;功能温度范围广;屏蔽时的稳定性——金属板屏蔽的代码可以读取;稳定的机械作用;小尺寸和低消耗,对于上一代的微纤维来说,具有特殊的性能,允许对信息进行磁编码的可能性):生成的代码量非常大;所述信息既可以从静止源读取,也可以从运动源读取;编码是不可能破坏的,无论是在粉末冶金和先进材料- RoPM&AM 2017材料研究论坛LLC材料研究进展8 (2018)1-10 doi: http://dx.doi.org/10.21741/9781945291999-1 2连续和可变磁场,(可靠编码);从空间中任意方向的代码中读取信息的可能性。纸的结构由植物纤维(木材或非木材)组成,其中加入了辅助材料,如填料,胶粘剂,颜料,添加剂等。根据纸张的应用领域,某些结构特征被施加到网络上:纤维-纤维接触的数量和纤维间空间的大小,表面的密度和粗糙度。这些属性根据识别性质、加工程度,辅助的数量和属性,和处理技术用于网络的形成和完成。填充物是指添加到纸浆中的任何非纤维材料,以改善纸张的光学性能,以及其他特征,如孔隙度、平滑度、印刷能力等。通过在纸浆中掺入颜料,增加了纸张的光学不均匀性,增加了纸张上的反射光和折射光,提高了纸张的白度和不透明度。同时,保留在薄片结构中的色素颗粒增加了纤维间的空间,减少了纤维间键形成的可能性,对纸张阻力指标产生了负面影响。填料在纸张中的保留主要是通过大颗粒的过滤和细颗粒的胶体现象来实现的。填料的引入主要取决于技术方面的考虑,因为如果只使用纤维材料,纸张的某些特性,特别是光学指数和印刷能力是有限的。目前,填料在某些情况下也可以作为纤维材料的部分替代品,从而有助于降低生产成本。采用Taylor-Ulitovsky工艺研制的gmw由外包玻璃绝缘层的圆柱形金属芯组成,金属芯的直径为350 μm,玻璃绝缘层的厚度为120 μm。这种微导线的长度,在实验室条件下,达到大约。1公里。铁磁玻璃包覆微线,切割在大约。 长度为7mm的微丝段在纸的组成中也作为填充材料,但在纸浆和纸张结构中,微丝段具有与传统填充材料不同的特定行为。与这些材料不同的是,将极少量的铁磁微线引入纸中,对浆料的流变特性和纸的电阻特性没有显著的影响。电线的外观、直径、长度和微线密度也是区分目前用于填充纸张的材料的具体特征。在铁磁微丝的情况下,保留效率的重要性主要是由于需要在纸张中达到一定的微丝密度,以确保其安全性而不影响纸张质量和功能。2. 制备gmw的泰勒-乌里托夫斯基技术是在玻璃管的高频电感中放置金属棒(图1)。在产生的电磁场的影响下,金属熔化,形成液滴。在与熔融金属接触时,玻璃管的一部分变软,覆盖液滴的玻璃形成涂层。对于一个特定的工作状态[11],这种玻璃浸泡通过拉也训练金属,导致微线的形成,这是收集在阀芯。可以得到不同的金属芯结构:不同尺寸的多晶晶体(微晶、纳米晶)或非晶。实验研究采用Fe77B13Si10 gmw,通过x射线衍射和磁性,通过振动样品磁强计,对其进行了结构表征。在纸张结构中达到一定的GMW密度,如填料,取决于造纸过程中对智能材料保留有特殊影响的因素的作用。了解和控制这些影响将最终使纸张达到足够的密度。在这方面,已经试验了粉末冶金和先进材料- RoPM&AM 2017年材料研究论坛有限责任公司材料研究学报8 (2018)1-10 doi: http://dx.doi.org/10.21741/9781945291999-1 3几个项目,其中实现gmw担保论文的基本配方已经补充了针对所研究的每个影响因素的几个变量。图1所示。Fe77B13Si10铁磁玻璃包覆微丝拉丝过程中的一个方面。表1。参数S/H比,[wt. %] S/H Schopper - Riegler度,[SR]微丝量,[g] Retentor量,[%]纸重,[g/m]纤维材料性质100 S或100 H 30 0.005;0.007;0.009纤维素材料的Schopper - Riegler度SR 60/40 30/20;40/30;50/40;60/50 0.009 GMWs量60/40 30/20;40/30;50/40;60/50 0005;0007;0009;0.011纸张纤维成分中的软木/硬木纤维素纸浆比例为20/80;30/70;40/60;50/50 45/30 0.007保留乳液量,在纸质制造单据中添加60/40 30/ 200;0.2;0.4;0.6;0.8纸张重量60/40 30/20 50;70;90;长度为7mm的gmw作为填料嵌入纤维素基质(纸浆)中,混合物的主要接收物(wt.%)为:从软木(S)纸浆中漂白的硫酸盐纤维素(不同量:30 - 100%;Schopper - Riegler度:30 - 60 SR);硬木(H)纸浆漂白硫酸盐纤维素(不同量:30 - 100%;Schopper - Riegler度20 50 SR);纸张填充材料:15%碳酸钙;胶乳:1.5%烷基二美塞烯(AKD);保留添加剂:0.5%聚酰胺胺和不同量的GMW(10张纸,纸重q = 75 g/m) - 0.005g;0.007克;0.009g和0.011g。选择纸张制备实验配方的特殊性,以突出不同粉末冶金和先进材料的影响- RoPM&AM 2017材料研究论坛LLC材料研究进展8 (2018)1-10 doi: http://dx.doi.org/10.21741/9781945291999-1 4个工艺参数(表1)。Schopper-Riegler试验提供了稀浆悬浮液脱水速率的度量。研究表明,滤干性与纤维的表面条件和膨胀有关,是衡量纸浆受到的机械处理程度的有用指标。保留效率(η)表示为最初用于制备纤维素糊的GMW量与实验室制备的纸张中剩余GMW量的比值(每次实验中,确定10张纸的保留率)。3.结果与讨论 Fe77B13Si10铁磁玻璃包覆微丝制备完成后,通过x射线衍射对其进行了结构表征。玻璃涂层是
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引用次数: 0
Obtaining of W/Cu nanocomposite powders by high energy ball milling process 高能球磨法制备W/Cu纳米复合粉体
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-20
V. Nicoară, F. Popa, T. Marinca, C. Nicolicescu
The morphology of the particles is important in the process of obtaining alloys based on W/Cu, thus this investigation is focused on the influence of the copper content on the properties of W/Cu nanocomposites powders obtained after 20 hours of high energy ball milling. The experimental results regarding the obtaining of W100-x/Cux nanocomposites (x between 20 and 45 wt. %) are presented. Composition of the mixtures influenced the particle size distribution namely, the higher is Cu content the larger dimensions of the particles will be attained. After 20 hours of high energy ball milling the crystallites size was about 30 nm for copper respectively 12 nm for tungsten and Cu atoms entered in the W structure. Introduction One of the specific classes of materials which are suitable for elaboration by Powder Metallurgy (PM) consists in pseudo-alloys based on W-Cu due to their mutual insolubility. These materials are very important due to their wide field of applicability such as: welding electrodes, nozzle liners for rockets and missiles, heat sink materials, high power electrical contacts, fission reactors and so on, applications that require high mechanical properties conferred, in this case by tungsten, combined with high electrical and thermal conductivity which are conferred by copper [1-6]. The properties of these materials are in correlation with their composition and morphology and because of that is very important to choose the right composition function of the application [7]. In the field of high power electrical contacts, W-Cu materials must have high arc erosion resistance high temperature strength and high tribological properties to ensure an as long as possible lifetime [8, 9]. Particle size of the component elements plays an important role in the final properties of WCu alloys [10]. One of the techniques used for fabrication of the W-Cu materials is the infiltration one, which consists in the formation of a porous skeleton by tungsten which will be filled with molten copper. Vacuum pulse carburisation was reported [11] to be an infiltration method that leads to the formation of W-30wt.%Cu material with core-shell structure which presents high electrical conductivity (46.55%IACS) compared to the national standard (GB/T8320-2003 – 42%IACS) and a friction coefficient μ=0.64. To improve the sinter ability of W-Cu materials it can be introduced some activators such as Ni, Fe or Co which can be grain growth inhibitors [12]. Using of this activators can lead to a decreasing of electrical and thermal conductivity of W-Cu Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 173-181 doi: http://dx.doi.org/10.21741/9781945291999-20 174 materials [13, 14]. A technique used for mass production which is suitable to produce W-Cu complex shape parts is Metal Injection Moulding (MIM) [15]. Another method to produce W-Cu materials is Mechanical Alloying (MA) which ensures obtaining
(2)给出了10分钟MM(休息2分钟)温度和压力的演变。粉末冶金与先进材料- RoPM&AM材料研究论坛有限责任公司2017材料研究论文集8 (2018)173-181 doi: http://dx.doi.org/10.21741/9781945291999-20 175从(图2)可以看出,由于为干磨型,温度不超过50℃,压力基本恒定。这些参数必须控制,因为如果温度过高,可能会损坏碗和设备。粉末混合物的形态学方面使用JEOL显微镜JSM-5600 LV。采用美国Brookhaven Instruments公司的90Plus粒度分析仪,配备波长为660 nm的35 mW固体激光器,采用动态激光散射(DLS)技术研究了粒径分布和多分散性的演变。温度为25℃,散射角为90°。在水中稀释粉末混合物,每个样品的溶液进行超声波处理5分钟,以避免颗粒絮凝。x射线衍射的研究是用Inel衍射仪进行的,型号为Equinox 3000,工作在反射和Co辐射中。2的研究间隔是20-110度。结果和讨论在(图3)中分别给出了初始均质混合物和研磨20小时样品的形貌。从(图3 a, c, e, g, i, k)可以明显看出,初始均质混合物中钨颗粒的粒径(纳米级)低于铜颗粒。此外,在(图3k)中可以观察到钨纳米粉对铜颗粒的覆盖程度较高,这与混合物的组成(80W/Cu)相一致。经过20小时的MM处理(图3 b, d, f, h, j, l),所有样品的元素个体形态都变为均匀状态。很可能实现了不同粒子的混合和焊接。而且粉末容易结块。图4为不同阶段混合物的XRD谱图。图中给出了未铣削样品和铣削5、10、15和20 h样品的W-Cu混合物的x射线衍射图。除了这些衍射图外,在同一图中还给出了W和Cu的平均晶粒尺寸随铣削时间的变化。粉末冶金与先进材料- RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 173-181 doi: http://dx.doi.org/10.21741/9781945291999-20 176来自Im-3m空间组,根据JCPDS文件04-0806和04-0836,在未研磨样品的x射线衍射图中可以观察到W - bcc结构的峰特征。图3所示。a) 55W/Cu均质混合物的SEM图像;b) MM 20小时后55W/Cu;c) 60W/Cu均质混合物;d) MM 20h后60W/Cu;e) 65W/Cu均质混合物;f) MM 20h后65W/Cu;g) 70W/Cu均质混合物;h) MM 20小时后70W/Cu;i) 75W/Cu均质混合物;j) MM 20h后75W/Cu;k) 80W/Cu均质混合物;l) MM 20h后80W/Cu;W和Cu峰强度的比值随着混合物中W和Cu含量的变化而变化,正如预期的那样。还可以观察到钨衍射峰的展宽,这是由于混合物中使用的钨粉的纳米晶状态。钨粉的平均晶粒尺寸(用Scherrer法计算)为12±2 nm。研磨5 h后,铜的衍射峰也变宽,表明铜的晶体减少。进一步增加铣削时间也会导致铜的衍射峰增大,直到铣削时间结束,在所有W和Cu之比的衍射图中都没有发现其他的衍射峰。可以观察到,与材料中Cu的含量无关,在衍射图中可以观察到其峰。研磨20 h后,材料中出现fcc铜基结构。已知在平衡条件下W和Cu之间没有溶解度,也知道通过机械铣削可以得到不混相元素之间的固溶体,可以假设经过20次铣削后,一些Cu原子进入了W结构。x射线研究表明,在铣削结束时,材料是由W-Cu固溶体和Cu纳米晶组成的纳米复合材料。可以注意到钨晶在与铜一起研磨时没有明显的变化。它保持在12±2 nm左右。 平均粉末冶金和先进材料- RoPM&AM 2017材料研究论坛LLC材料研究论文集8 (2018)173-181 doi: http://dx.doi.org/10.21
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引用次数: 2
Atomic force microscopy analyses on metallic thin films for optical MEMS 光学MEMS金属薄膜的原子力显微镜分析
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-14
V. Merie, M. Pustan, G. Negrea, C. Bîrleanu
This paper is a study on three metallic thin films usable for manufacturing optical MEMS. The films were deposited by thermal evaporation on glass substrates. They were characterized from the topographical, tribological and mechanical point of view at nanoscale. The results pointed out that the silver thin films present higher values of the tribological and mechanical properties than the other two films when testing at room temperature. Increasing the testing temperature from 20 to 100 °C caused a decreased of both hardness and Young’s modulus with about 30 up to 55 %. Introduction The optical microelectromechanical systems (MEMS) are formed in general by multi-layers of metallic thin films characterized by good optical properties. Over the last decades, the attention of the researchers was focused on developing different devices known as microelectromechanical systems (MEMS) that are satisfying the demands of the customers. The properties of the materials employed for manufacturing such devices determine its properties and its performance [1]. The optical MEMS are a category of MEMS devices that are combining the optical, mechanical, and electronic properties in a single device. They are used in the manufacture of optical sensors, attenuators, micro-lenses, micro-mirrors, displays and so on [2-5]. Aluminum [6, 7], gold [8, 9] and silver [10, 11] are one of the most used materials for manufacturing optical MEMS due to their physical, chemical, mechanical, and optical properties. These materials can be obtained as thin films by different methods such as thermal evaporation [6], magnetron sputtering [7-9], electron beam deposition [12], and so on. Arrazat and his colleagues reported their results concerning the evolution of gold thin films deposited by sputtering on silicon substrates. They investigated the deposited films by electron back scatter diffraction analyses that allowed them to study the reliability of micro-switches manufactured using gold thin films [13]. The growth of aluminum thin films and the interfacial precipitation between such films and the silicon substrates were studied by Dutta and his coworkers. They pointed out that at the interface between the aluminum thin films and the silicon substrate during the heat treatment, some silicon precipitates are formed. According to them, these precipitates are supplying the driving force necessary for the deposit of the aluminum thin films [14]. Hojabri and his team worked on determining the influence of substrate temperature on the morphological and structural characteristics of silver thin films deposited by direct current magnetron sputtering on silicon substrates. Their results showed that the substrate temperature Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 125-133 doi: http://dx.doi.org/10.21741/9781945291999-14 126 strongly influence the growth of the silver thin films, their surface roughness, as well
本文研究了三种可用于制造光学MEMS的金属薄膜。薄膜是通过热蒸发沉积在玻璃衬底上的。从形貌、摩擦学和力学角度对其进行了表征。结果表明,在室温条件下,银薄膜的摩擦学性能和力学性能均高于其他两种薄膜。将测试温度从20℃提高到100℃,硬度和杨氏模量都下降了约30%至55%。光学微机电系统(MEMS)一般是由具有良好光学性能的多层金属薄膜构成的。在过去的几十年里,研究人员的注意力集中在开发不同的器件,即微机电系统(MEMS),以满足客户的需求。用于制造这种装置的材料的性质决定了它的性质和性能[1]。光学MEMS是将光学、机械和电子特性结合在单个器件中的一类MEMS器件。它们被用于制造光学传感器、衰减器、微透镜、微镜、显示器等[2-5]。铝[6,7]、金[8,9]和银[10,11]由于其物理、化学、机械和光学性能,是制造光学MEMS最常用的材料之一。这些材料可以通过热蒸发[6]、磁控溅射[7-9]、电子束沉积[12]等不同的方法得到薄膜。Arrazat和他的同事报告了他们关于在硅衬底上溅射沉积金薄膜的演变的结果。他们通过电子反向散射衍射分析研究了沉积的薄膜,这使他们能够研究使用金薄膜[13]制造的微开关的可靠性。Dutta和他的同事研究了铝薄膜的生长和这种薄膜与硅衬底之间的界面沉淀。他们指出,在热处理过程中,铝薄膜与硅衬底之间的界面处形成了一些硅沉淀。他们认为,这些沉淀物为铝薄膜b[14]的沉积提供了必要的驱动力。Hojabri和他的团队致力于确定衬底温度对在硅衬底上通过直流磁控溅射沉积的银薄膜的形态和结构特征的影响。他们的研究结果表明,衬底温度对银薄膜的生长、表面粗糙度和晶粒尺寸[15]有很大的影响。粉末冶金与先进材料- RoPM&AM 2017材料研究论坛LLC材料研究进展8 (2018)125-133 doi: http://dx.doi.org/10.21741/9781945291999-14 126。本研究是对热蒸发法在玻璃基板上沉积铝、金、银薄膜的实验研究,这些薄膜适合制造光学MEMS。材料和实验方法采用纯度为99.99%的铝靶、金靶和银靶热蒸发法制备了三种金属薄膜。薄膜被沉积在玻璃衬底上。底物用高纯度酒精(99.9%)在超声波浴中清洗,以去除任何可能的杂质。然后用压缩空气吹。我们使用电阻加热钨源(“船”型)和真空气氛(5.10托)。施加了60- 80a的电流。衬底与电阻器之间保持50mm的恒定距离。用克卢日纳波卡工业大学材料科学与工程系的JEOL JSM 5600 LV扫描电子显微镜测定了沉积薄膜的厚度约为70 nm。从形貌、摩擦学和力学等方面对制备的薄膜进行了表征。测试在克卢纳波卡技术大学微纳米系统实验室的XE70原子力显微镜(AFM)上进行,环境干净。采用n型硅NSC35C悬臂梁对三种金属薄膜的形貌和摩擦学特性进行了研究。其特点如厂家所述:长度为130 μm,厚度为2 μm,宽度为35 μm,力常数为5.4 N/m。测试时使用的设定点为10 nN。采用点内光谱法,利用PPP-NCHR悬臂梁实现了附着参数的测定。相对湿度为31%,测试温度在20 ~ 100℃之间变化,每次测试增加20℃。
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引用次数: 0
Reactive mechanical milling of Fe-Ni-Fe2O3 mixtures Fe-Ni-Fe2O3混合物的反应机械铣削
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-3
T. Marinca, N. Sechel, I. Chicinaș, F. Popa, H. Chicinaş, B. Neamțu
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引用次数: 0
Mössbauer spectroscopic analysis of (Nd,Pr,Dy)2(Fe,Co,Ga)14B/α-Fe permanent magnetic nanocomposites Mössbauer (Nd,Pr,Dy)2(Fe,Co,Ga)14B/α-Fe永磁纳米复合材料的光谱分析
Pub Date : 2018-11-05 DOI: 10.21741/9781945291999-8
E. Manta, B. Cekić, V. Ivanovski, A. Umićević, Katarina Ćirić
In this paper, it is reported the structural and magnetic properties of Nd13.7Pr0.7Dy0.2Fe73.1Co6.3Ga0.4B5.6 and Nd7.7Pr0.7Dy0.2Fe79.1Co6.3Ga0.4B5.6 magnetic nanocomposites, synthesized by melt-spinning and annealing methods. The Nd-Fe-B ribbons are melt-spun at v=30 m/s in high vacuum and annealed at 715C for 4 min. in argon. Furthermore, Xray diffraction and transmission Fe Mössbauer spectra at RT are used to investigate the effects of substituent elements: Dy, Pr, Co, Ga on the hard magnetic properties and microstructure of both nanocomposites. Analysis of Mössbauer spectra for Nd13.7Pr0.7Dy0.2Fe73.1Co6.3Ga0.4B5.6 is done in terms of ten Zeeman sextets, one paramagnetic doublet related to Nd1.1Fe4B4 phase and two hyperfine magnetic fields distributions extracted from spectrum. Similar result of analysis of the second nanocomposite is obtained with eleven sextets, one doublet and one distribution. One sextet corresponds to α-Fe phase, while we have identified six iron sextets corresponding to the six distinct iron sites in the Nd2Fe14B structure: 16k1, 16k2, 8j1, 8j2, 4c and 4e. The three remaining sextets belong to Fe3B structure with three inequivalent Fe sites: FeI(8g), FeII(8g) and FeIII(8g). The eleventh sextet of Nd7.7Pr0.7Dy0.2Fe79.1Co6.3Ga0.4B5.6 belongs to FeB. All relevant parameters for both nanocomposites: magnetic hyperfine field, isomer shift and quadrupole splitting are determined for each of these sites. To highlight the thermally induced structural transformations, the quenched samples have been analysed by differential scanning calorimetry and thermomagnetic measurements. The magnetic properties, measured at RT on the quenched and annealed ribbons, revealed the relationship between the alloy chemical composition and processing.
本文报道了采用熔融纺丝和退火法制备的Nd13.7Pr0.7Dy0.2Fe73.1Co6.3Ga0.4B5.6和nd7.7 pr0.7 dy0.2 fe70.1 co6.3 ga0.4 b5.6磁性纳米复合材料的结构和磁性能。Nd-Fe-B带在高真空中以v=30 m/s的速度熔融纺丝,并在715℃氩气中退火4 min。此外,利用x射线衍射和透射Fe Mössbauer在RT下的光谱研究取代元素:Dy, Pr, Co, Ga对两种纳米复合材料的硬磁性能和微观结构的影响。对Nd13.7Pr0.7Dy0.2Fe73.1Co6.3Ga0.4B5.6的Mössbauer光谱进行了10个Zeeman六重体、1个与Nd1.1Fe4B4相相关的顺磁偶极体和从光谱中提取的2个超精细磁场分布的分析。第二种纳米复合材料具有11个六重体、1个双重体和1个分布,得到了类似的分析结果。一个六元体对应α-Fe相,而我们已经确定了六个铁六元体对应于Nd2Fe14B结构中的六个不同的铁位点:16k1, 16k2, 8j1, 8j2, 4c和4e。其余三种六元体属于Fe3B结构,具有三个不相等的铁位:FeI(8g), FeII(8g)和FeIII(8g)。nd7.7 pr0.7 dy0.2 fe70.1 co6.3 ga0.4 b5.6的第11个六重体属于feb,并确定了这两种纳米复合材料的相关参数:超精细磁场、同分异构体位移和四极分裂。为了突出热诱导的结构转变,用差示扫描量热法和热磁测量对淬火样品进行了分析。对淬火带和退火带的磁性能进行了RT测量,揭示了合金的化学成分与加工过程之间的关系。
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Powder Metallurgy and Advanced Materials
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