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Effect of Agitation Methods on Characteristics of Iron Ferrite Nanoparticles Synthesized by Co-Precipitation Process 搅拌方式对共沉淀法合成铁酸铁纳米颗粒特性的影响
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0005
H. R. Dehghanpour, P. Parvin, A. Younesi, Monireh Gilaki
To assess the result of the stirring process on the Fe3O4 nanoparticles' properties, two types of stirrings (mechanical and magnetic) were compared. Fe3O4 nanoparticles were generated by chemical precipitation. Oleic acid covered the nanoparticles as a surfactant performer. X-ray diffraction (XRD) was used to investigate the fine grains sample, and scanning electron microscope (SEM) images were used for observing the nanoparticles’ geometry. The vibrating sample magnetometer (VSM) was also used to examine the magnetic characteristic of the nanoparticles. Chemical bonds were determined by using Fourier transform infrared spectroscopy (FTIR). As a result, the hysteresis loop characterized the magnetic nanoparticles. Magnetite nanoparticles are regarded as a soft magnetic material due to their low coercivity. XRD diagrams show the presence of powerful peaks in the orientations of crystal surfaces of the spinel form of the nanoparticles. The result showed that nanoparticles were nearly spherical. The average dimensions of the nanoparticles were estimated by Scherrer approximation. The mean particle dimensions were 11 nm (chemical mixer) and 13 nm (magnet mixer). SEM images verified the spherical shape of the nanoparticles, and FTIR confirmed the constitution of Fe-O bonds and validated the spinel ferrites configuration.
为了评估搅拌过程对Fe3O4纳米颗粒性能的影响,比较了两种搅拌方式(机械搅拌和磁力搅拌)。采用化学沉淀法制备了纳米Fe3O4。油酸作为表面活性剂覆盖在纳米颗粒表面。利用x射线衍射(XRD)对样品进行表征,利用扫描电镜(SEM)对纳米颗粒的形貌进行观察。用振动样品磁强计(VSM)检测了纳米颗粒的磁性特性。用傅里叶变换红外光谱(FTIR)测定化学键。因此,磁滞回线表征了磁性纳米颗粒。磁性纳米颗粒由于其低矫顽力而被认为是一种软磁材料。XRD图显示,尖晶石型纳米颗粒的晶面取向存在强大的峰。结果表明,纳米颗粒接近球形。采用Scherrer近似估计了纳米颗粒的平均尺寸。平均粒径为11 nm(化学混合器)和13 nm(磁力混合器)。SEM图像证实了纳米颗粒的球形,FTIR证实了Fe-O键的构成,并证实了尖晶石铁素体的结构。
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引用次数: 0
Temperature-dependent Photoluminescence Properties of Eu2+-doped CaMgSi2O6 Phosphors Eu2+掺杂CaMgSi2O6荧光粉的温度依赖性光致发光特性
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0004
T. Wu, Guoxiang Peng, Wei-Ren Zhang, Cheng-Fu Yang
The solid-state reaction method was used to synthesize 0.025Eu2+-doped CaMgSi2O6 (Eu-CaMgSi2O6) powder in the reduction atmosphere of 5% H2 + 95% N2 at 1300oC with a duration of 4 h. The reduction atmosphere was removed when the temperature was down to 800oC. The XRD pattern showed that only the CaMgSi2O6 phase was observed in synthesized 0.025Eu2+-doped CaMgSi2O6 powder. Room-temperature photoluminescence excitation (PLE) and photoluminescence (PL) spectra of Eu-CaMgSi2O6 phosphors were recorded by using the Hitachi F-4500 fluorescence spectrophotometer at wavelength ranges of 200–430 and 350–600 nm, respectively. A new important finding is that the synthesized Eu-CaMgSi2O6 phosphor has three important PLE wavelengths. Therefore, Eu-CaMgSi2O6 phosphors are measured from 25oC (room temperature) to 200oC under three different PLE wavelengths to find the effect of temperature on the variations of maximum photoluminescence intensities (PLmax). All the PL spectra show that only one emission band with a central wavelength of 449 nm is found, which is independent of the PLE wavelengths and is caused by the transition of 4f7 → 4f65d1. Another important finding is that the different PLE wavelengths have an apparent effect on the PLmax value of the Eu-CaMgSi2O6 phosphor. Finally, the decay-time curves of Eu-CaMgSi2O6 phosphor under three PLE wavelengths are also investigated.
采用固相反应法,在5% H2 + 95% N2还原气氛下,在1300℃下合成0.025Eu2+掺杂CaMgSi2O6 (Eu-CaMgSi2O6)粉体,反应时间为4 h,温度降至800℃时去除还原气氛。XRD谱图表明,合成的0.025Eu2+掺杂CaMgSi2O6粉体中只存在CaMgSi2O6相。利用日立F-4500荧光分光光度计分别记录了Eu-CaMgSi2O6荧光粉在200 ~ 430 nm和350 ~ 600 nm波长范围内的室温光致发光激发(PLE)和光致发光(PL)光谱。一个新的重要发现是,合成的Eu-CaMgSi2O6荧光粉具有三个重要的PLE波长。因此,在25℃(室温)至200℃范围内,在三种不同的PLE波长下测量Eu-CaMgSi2O6荧光粉,以寻找温度对最大光致发光强度(PLmax)变化的影响。所有的PL光谱都表明,只有一个中心波长为449 nm的发射波段与PLE波长无关,是由4f7→4f65d1跃迁引起的。另一个重要的发现是,不同的PLE波长对Eu-CaMgSi2O6荧光粉的PLmax值有明显的影响。最后,研究了铕- camgsi2o6荧光粉在三个PLE波长下的衰减时间曲线。
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引用次数: 1
Study on Preparing β-Ga2O3 Films with Temperature-Controlled Buffer Layer by RF Magnetron Sputtering 射频磁控溅射制备具有温控缓冲层的β-Ga2O3薄膜的研究
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0003
Yi Liu, T. He, Sufen Wei
β-Ga2O3 thin films were prepared on (0006) sapphire substrates by RF magnetron sputtering. Under the conditions of sputtering power of 80 W, time of 10 min, and total flow rate of 40 sccm in oxygen and argon atmosphere (2.5 % oxygen ratio). Different preparation temperatures were used to conduct layering by temperature modulation. A homogenous β-Ga2O3 buffer layer was grown first, and then the second β-Ga2O3 film was grown on top of it. When the stratified sputtering of different temperature combinations was completed, high-temperature thermal annealing with the same parameters was performed. The effects on the structure, surface morphology, and optical properties of β-Ga2O3 thin films were compared and analyzed when using the preparation sequence of the homogenous buffer layer and the top layer at different temperatures after annealing. Finally, based on the stratified preparation temperature parameters, the optimal stratified temperature parameters were summarized.
采用射频磁控溅射技术在(0006)蓝宝石衬底上制备了β-Ga2O3薄膜。溅射功率为80 W,溅射时间为10 min,总流量为40 sccm,在氧气和氩气中(氧气比为2.5%)溅射。采用温度调制的方法,利用不同的制备温度进行分层。先生长一层均匀的β-Ga2O3缓冲层,再在其上生长第二层β-Ga2O3薄膜。当不同温度组合的分层溅射完成后,进行相同参数的高温热退火。比较分析了退火后均匀缓冲层和顶层在不同温度下的制备顺序对β-Ga2O3薄膜结构、表面形貌和光学性能的影响。最后,根据分层制备温度参数,总结出最佳的分层温度参数。
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引用次数: 0
Nanostructuring Polyaniline Using Non-Substituted Imidazolium-Based Ionic liquid as Polymerization Medium Enabling Faster Supercapacitor Operation 以非取代咪唑基离子液体为聚合介质制备纳米聚苯胺,使超级电容器运行速度更快
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0001
Fatima Al Zohbi, F. Ghamouss, B. Schmaltz, M. Abarbri, K. Cherry, Mohamad fadel Tabcheh, F. Tran Van
Non-substituted imidazolium-based protic ionic liquid, namely imidazolium hydrogen sulfate [Imi][HSO4], has been investigated as a polymerization medium for PANI (designated as PANI/PIL). The resulting material was then investigated as electrode materials for supercapacitors. [Imi][HSO4] was prepared via a one-step acid-base reaction, and its structure was confirmed by 1H NMR. [Imi][HSO4] displayed full miscibility with water owing to the charge density distribution of its ions. Furthermore, the binary mixture [Imi][HSO4]/water is highly acid (e.g. pH ~ 0.1 for [Imi][HSO4]/water in a weight ratio of 70/30). As the polymerization medium for PANI/PIL, [Imi][HSO4] plays the role of a soft template agent and induces nanostructured PANI formation with fibrillar morphology (as shown by SEM images) without affecting the typical structure of PANI (as confirmed by FT-IR analysis). Furthermore, PANI/PIL was obtained in emeraldine salt form without any undesirable byproduct. Moreover, the electrical conductivity was seven times superior to that of the conventional PANI (i.e. PANI/HCl) when measured by the four-probe technique of PANI/PIL (~ 21.8 S/cm). This improvement in the PANI/PIL’s electrical conductivity of as well as the fibrillar morphology of PANI/PIL positively influences its electrochemical performances and highlights the suitability of [Imi][HSO4] as a polymerization medium for PANI material.
研究了非取代咪唑基质子离子液体,即咪唑硫酸氢[Imi][HSO4]作为聚苯胺(简称PANI/PIL)的聚合介质。然后研究了所得材料作为超级电容器的电极材料。通过一步酸碱反应制备了[Imi][HSO4],并通过1H NMR对其结构进行了证实。[Imi][HSO4]由于其离子的电荷密度分布,与水表现出完全的混溶性。此外,[Imi][HSO4]/水二元混合物呈强酸性(如[Imi][HSO4]/水在70/30的质量比下pH ~ 0.1)。[Imi][HSO4]作为聚苯胺/PIL的聚合介质,起到软模板剂的作用,在不影响聚苯胺典型结构的情况下,诱导形成具有纤维状形态的纳米结构聚苯胺(如SEM图像所示)(经FT-IR分析证实)。此外,聚苯胺/太平盐以翡翠盐的形式得到,没有任何不良的副产物。此外,用四探针法测定的电导率(~ 21.8 S/cm)比传统聚苯胺(即聚苯胺/盐酸)高7倍。PANI/PIL的电导率和纤维状形态的改善对其电化学性能产生了积极的影响,并突出了[Imi][HSO4]作为PANI材料聚合介质的适用性。
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引用次数: 0
Clinical Significance of Accurate Transfer of Provisional Resin-Based to Permanent Lithium Disilicate Glass Ceramic Dental Restorations 临时树脂基到永久二硅酸锂玻璃陶瓷牙体准确转移的临床意义
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0002
Evangelos Ximinis, Maria Tsiafitsa, O. Naka, D. Dionysopoulos
Smile reconstruction is, yet, a challenging procedure for dental practitioners. A stable and satisfactory aesthetic result demands a meticulous procedure, which involves many clinical and laboratory steps. The purpose of this article is to present a case of aesthetic reconstruction in the anterior region with a successful 14-year recall. A 40-year-old female patient came to the dental clinic complaining about her smile appearance. Lithium disilicate glass-ceramic full-coverage restorations for the six upper anterior teeth were the selected treatment plan for this case. The key to this successful result was the used therapeutic methodology, where the characteristics of the provisional restorations were copied to the final restorations. In this article, the therapeutic methodology is presented step by step and all the clinical and laboratory steps are explained thoroughly. The patient has visited the dental clinic annually as arecall visit. The final result from the 14-year recall visit revealed that the aesthetic result was stable, the restorations were intact and there were no signs of gingival infection or dental decay. Consequently, the presented therapeutic methodology leads to a successful and long-term result.
然而,对牙科医生来说,重建微笑是一个具有挑战性的过程。一个稳定和满意的美学结果需要一个细致的程序,包括许多临床和实验室步骤。这篇文章的目的是提出一个案例美学重建在前区与成功的14年回忆。一位40岁的女病人来到牙科诊所,抱怨自己的笑容。本病例选择六颗上前牙的二硅酸锂玻璃陶瓷全覆盖修复方案。这一成功结果的关键是使用的治疗方法,其中临时修复体的特征被复制到最终修复体中。在本文中,逐步介绍了治疗方法,并对所有临床和实验室步骤进行了彻底的解释。这个病人每年去牙科诊所一次,作为回忆。14年的召回访问的最终结果显示,美观结果稳定,修复体完好无损,没有牙龈感染或蛀牙的迹象。因此,提出的治疗方法导致一个成功的和长期的结果。
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引用次数: 0
Novel Schiff Base Co(II) Complexes: Potential Biological Applications 新型希夫碱Co(II)配合物:潜在的生物学应用
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-09-30 DOI: 10.35745/afm2022v02.03.0006
Arumugam Parasuraman Arumugam, Govindan Elango, S. Guhanathan
Cobalt (Co) complexes with the N2O2 category have been created synthetically by the reaction of salicylaldehyde / 3,4-diamino benzophenone with acetylacetone and glutaric anhydride respectively. The ligands and individual Cobalt (II) complexes were recognized through spectroscopical data (Fourier Transform Infrared, Ultra Violet-visible, proton and carbon-13 NMR, & Mass). Non-electrolytic in nature of the complex found from their molar conductivities (Ω-1cm2mol-1) in DMSO of 10-3M solution. The ESR revealed the geometry of the complexes to be octahedral. The Schiff base Cobalt (II) complex was characterized by anticancer activity and cytotoxicity
以水杨醛/ 3,4-二氨基苯甲酮为原料,分别与乙酰丙酮和戊二酸酐反应合成了N2O2类钴配合物。配体和单个钴(II)配合物通过光谱数据(傅里叶变换红外,紫外可见,质子和碳-13核磁共振,和质量)被识别。非电解性质的配合物发现,从他们的摩尔电导率(Ω-1cm2mol-1)在DMSO的10-3M溶液。ESR显示配合物的几何形状为八面体。希夫碱钴(II)配合物具有抗癌活性和细胞毒性
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引用次数: 0
Photovoltaic Performance of CH3NH3PbI2Cl Perovskite Solar Cell CH3NH3PbI2Cl钙钛矿太阳能电池的光伏性能
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-06-30 DOI: 10.35745/afm2022v02.02.0003
Yi-Tzu Tseng, Y. Tseng, C. Wu
Perovskite solar cells have attracted extensive research attention recently as they are promising high-performance solar cells with long-time stability at a low cost. In this study, we demonstrated a one-step solution approach to prepare the CH3NH3PbICl2 perovskite layer by adding lead chloride (PbCl2) to the standard methylamine iodide (MAI) precursor solution and annealing process of the perovskite layer at different temperature. Finally, the Ag/Spiro-OMeTAD/CH3NH3PbI2Cl /mp-TiO2/c-TiO2/FTO/Glass perovskite solar cell was successfully fabricated by using solution processing.
钙钛矿太阳能电池是一种具有低成本、长时间稳定性的高性能太阳能电池,近年来引起了广泛的研究关注。在本研究中,我们通过在标准碘化甲胺(MAI)前驱体溶液中加入氯化铅(PbCl2),并在不同温度下对钙钛矿层进行退火处理,一步法制备了CH3NH3PbICl2钙钛矿层。最后,采用溶液法制备了Ag/Spiro-OMeTAD/CH3NH3PbI2Cl /mp-TiO2/c-TiO2/FTO/Glass钙钛矿太阳能电池。
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引用次数: 0
Electromechanical Property Calculation of Carbon Nanotubes Using Linear Augmented Cylindrical Wave Method 线性增广柱面波法计算碳纳米管机电性能
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-06-30 DOI: 10.35745/afm2022v02.02.0006
P. D’yachkov
Deformations of single-walled carbon nanotubes (SWNTs) change their band structure in the nanoelectromechanical systems. In this study, we investigated the response of the electronic structure of chiral and nonchiral SWNTs (8,7), (9,6), (10,5), (7,7), (11,0), (12,0), and (13,0) to twisting and axial tension modes by using the symmetrized linear augmented cylindrical wave technique. We showed that perturbations of the band structures depend on a “family” index p = (n1 − n2)mod 3 (where p = −1, 0 or 1). Twisting the semiconducting (8,7) tubule with p = 1 in the direction of the screw axis is accompanied by the large broadening of minimum gap E11 and narrowing of the second gap E22, while these gaps drastically change in the tubule (10,5) with p = −1. In these tubules, changing the direction of twisting leads to the reversal in direction of the gap shifts. Regardless of the twisting direction, in metallic (7,7) and quasi-metallic (9,6) SWNTs with p = 0, the E11 gap rapidly increases from 0.0 and 0.035 eV to about 1 eV. When twisting the zigzag tubules (13,0) p = 1 and (11,0) p = −1, the gaps E11 equal to about 0.8 eV increase and decrease by several hundredths of eV. On the contrary, the compression and extension of these tubules cause a sharp change in their band structure with approximately a twofold change in the gaps E11 and E22 and inversion in the sequence of the boundary bands. The similar deformation of the armchair nanotube (7,7) has practically no effect on its electronic levels. In the case of zigzag (12,0) p = 0 SWNT, all deformation modes transform the quasi-metallic tubule into the semiconductor.
单壁碳纳米管(SWNTs)的变形改变了其在纳米机电系统中的能带结构。在这项研究中,我们研究了手性和非手性swcnts(8,7)、(9,6)、(10,5)、(7,7)、(11,0)、(12,0)和(13,0)的电子结构对扭曲和轴向张力模式的响应。我们证明了能带结构的扰动依赖于“族”指数p = (n1−n2)mod 3(其中p = - 1,0或1)。在螺旋轴方向上扭曲半导体(8,7)管p = 1时,伴随着最小间隙E11的大幅扩大和第二间隙E22的缩小,而这些间隙在p = - 1时的管(10,5)中发生了急剧变化。在这些小管中,扭转方向的改变会导致间隙位移方向的逆转。无论扭转方向如何,在p = 0的金属(7,7)和准金属(9,6)SWNTs中,E11隙从0.0和0.035 eV迅速增加到约1 eV。当扭曲(13,0)p = 1和(11,0)p = - 1时,约为0.8 eV的间隙E11增加和减少了百分之几eV。相反,这些小管的压缩和拉伸使其能带结构发生了急剧变化,E11和E22的间隙发生了大约两倍的变化,边界带序列发生了反转。扶手椅纳米管的类似变形(7,7)实际上对其电子水平没有影响。在锯齿形(12,0)p = 0 SWNT的情况下,所有变形模式都将准金属管转变为半导体。
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引用次数: 1
Modeling of Optical Characteristics of Silver Nanoparticles—Water Suspension Subject to Electromagnetic Irradiation 纳米银粒子的光学特性建模——电磁辐照下的水悬浮液
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-06-30 DOI: 10.35745/afm2022v02.02.0004
H. R. Dehghanpour
Electromagnetic radiation on the suspension of silver-water nanoparticles was simulated using Maxwell equations and the phenomenological equation of extinction crosssection and application of appropriate boundary conditions for nanoparticles with spherical geometry. The outputs of this simulation (extinction coefficient in different conditions) were compared with previous experimental results. The similarity between the simulation outputs and the experimental results indicates the high degree of reliability of the simulation method to predict the results of situations in which there is no experimental data.
采用麦克斯韦方程和消光截面的现象学方程,并应用球形纳米粒子适当的边界条件,模拟了电磁辐射对银水纳米粒子悬浮液的影响。将模拟结果(不同条件下的消光系数)与以往的实验结果进行了比较。仿真输出与实验结果的相似性表明,该仿真方法对无实验数据情况下的结果预测具有很高的可靠性。
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引用次数: 0
Analogy among Center of Gravity, Center of Mass, and Centroid of Rigid body: Analysis of Formula for Their Respective Calculation as per Configuration of Body and Utilization in Composite Application 刚体重心、质心、质心的类比:按体形各自计算公式分析及在复合应用中的应用
IF 2.5 4区 医学 Q2 Biochemistry, Genetics and Molecular Biology Pub Date : 2022-06-30 DOI: 10.35745/afm2022v02.02.0002
Saransh Tiwari, Sudhaker Dixit, Ved Kumar, A. Rastogi
The essential distinctions and similarities between the center of gravity, the center of mass, and the centroid of a rigid body in space are illustrated in this article. The use of an acceptable equation for a given configuration of the body situated at any location in a 3-D space is established and used in a composite application in the boiler lever safety valve.
本文阐述了空间中刚体的重心、质心和质心之间的本质区别和相似之处。建立了在三维空间中任意位置的给定结构的可接受方程的使用,并在锅炉杠杆安全阀的复合应用中使用。
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引用次数: 1
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Journal of Applied Biomaterials & Functional Materials
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