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Corrosion Control of Aluminium Alloy in Alkaline Solution Using Some Leave Extracts 叶片提取物对铝合金在碱性溶液中的腐蚀控制
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20110102.12
L. Nnanna, I. Anozie, C. Akoma, I. M. Mejeha, K. Okeoma, K. I. Mejeh
The effect of Euphorbia hirta and Dialum guineense leave extracts on the corrosion of aluminium in 0.25M NaOH was investigated using gravimetric technique. It was shown that the presence of Euphorbia hirta and Dialum guineense leave extracts inhibited the corrosion of aluminium in the test solutions and that the inhibition efficiency depended on the concentration of the plant extract as well as on the time of exposure of the aluminium samples in 0.25M NaOH solu- tions containing the extracts. Dialum guineense extract shows the best inhibition capability for aluminium corrosion in so- dium hydroxide, probably, this is due to the planer orientation of the adsorbed extract molecules. Inhibition efficiency of the inhibitors tested increases with decreasing sodium hydroxide concentrations. The experimental data complied to both Langmuir and Temkin adsorption isotherms and the value and sign of the apparent activation energy of adsorption obtained suggests that inhibitor molecules have mixed inhibition mechanism.
采用重量法研究了大戟叶和豚鼠叶提取物对铝在0.25M NaOH中腐蚀的影响。结果表明,大戟叶提取物和豚草叶提取物对铝的腐蚀有抑制作用,其抑制作用取决于植物提取物的浓度和铝样品在含提取物的0.25M NaOH溶液中的暴露时间。Dialum guineense提取物对氢氧化钠中铝的缓蚀性能最好,这可能是由于其吸附的提取物分子取向呈平面状。随着氢氧化钠浓度的降低,所测试的抑制剂的抑制效率提高。实验数据符合Langmuir和Temkin吸附等温线,得到的吸附表观活化能值和符号表明,抑制剂分子具有混合抑制机制。
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引用次数: 9
Microstructural Analysis of Selected Corroded Materials from Nigeria Oil and Gas Industry 尼日利亚石油天然气工业腐蚀材料的微观结构分析
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20110102.18
O. Ajide, A. Makinde
The enormous financial loss and the problems of plants shut down, lost production, product loss, product contaminations and loss of customer confidence as a result of corrosion is a serious challenge to the oil and gas industry. The objective of this paper is to investigate the microstructural characteristics of selected corroded materials from Nigeria oil and gas environments. A chemical analysis of the selected corroded materials was carried out with the aid of spectro-metal analyzer. Also, the microstructures of these corroded materials were examined under optical microscope. The results obtained were compared with the chemical compositions and microstructures of the standard alloy of the as received materials .Significant variations were noticed both in the chemical compositions and the ferrite/pearlite ratio within the microstructure. It is concluded that corrosion has added some undesirable features to the material samples and altered the microstructure characteristics which will remarkably alters their mechanical properties.
由于腐蚀导致的工厂关闭、生产损失、产品损失、产品污染和客户信心丧失等巨大的经济损失和问题,是油气行业面临的严峻挑战。本文的目的是研究尼日利亚油气环境中选定的腐蚀材料的微观结构特征。利用金属光谱分析仪对选定的腐蚀材料进行了化学分析。并在光学显微镜下观察了腐蚀材料的显微组织。将所得结果与接收材料的标准合金的化学成分和显微组织进行了比较,发现化学成分和显微组织中的铁素体/珠光体比都发生了显著变化。结果表明,腐蚀使材料样品增加了一些不良特征,并改变了其显微组织特征,从而显著改变了材料的力学性能。
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引用次数: 6
On Anomalies of Electrical Conductivity in Antistatic Plasticized Poly(Vinyl Chloride) Films 抗静电增塑型聚氯乙烯薄膜电导率异常研究
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20110102.21
D. Vlasov, L. Apresyan, T. V. Vlasova, V. Kryshtob
In plasticized poly(vinylchloride) (PVC) films, representing system of two chemically non-interacting insula- tors, PVC and plasticizer, at monotonous increase of concentration of one of the insulators (plasticizer) sharp transition insulator-semiconductor to a "high" conductive state is found out, which is accompanied by similar transition back to state with low conductivity at further increase of plasticizer concentration. The observed concentration range with a "high" (semiconductor) level of electric conductivity permits us to measure the resistance-thickness dependence for relatively wide films thickness set (20-200 µm), which is close to simple exponential. A phenomenological model that allows to interpret the observed phenomena as "direct" and "inverse" percolation transitions in two-phase medium with charge-transfer by nano-scale kinetic segments of macromolecules mainly along the borders between PVC-clusters and plasticizer is proposed.
在增塑型聚氯乙烯(PVC)薄膜中,当其中一种绝缘子(增塑剂)的浓度单一增加时,绝缘子-半导体向“高”导电性状态急剧过渡,而当增塑剂浓度进一步增加时,绝缘子-半导体又迅速向低导电性状态过渡。观察到的具有“高”(半导体)电导率水平的浓度范围使我们能够测量相对宽的薄膜厚度集(20-200µm)的电阻-厚度依赖关系,该关系接近简单指数。提出了一个现象学模型,该模型允许将所观察到的现象解释为两相介质中的“直接”和“逆”渗透转变,并主要沿着pvc团簇和增塑剂之间的边界通过大分子的纳米级动力学片段进行电荷转移。
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引用次数: 8
Preparation and Characterization of Polyaniline-Co 3 O 4 Nanocomposites via Interfacial Polymerization 界面聚合法制备聚苯胺-氧化钴纳米复合材料及其表征
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120203.01
M. Bedre, R. Deshpande, Basavaraja Salimath, V. Abbaraju
Polyaniline (Pani) and Polyaniline-Co3O4 nanocomposites (PCO) were prepared by employing interfacial po- lymerization using ammonium persulphate as an oxidizing agent. The formations of regular nanocomposite materials were studied by Fourier transform infrared (FTIR) spectroscopy and XRD techniques. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images were conducted to characterize the morphology. Thermo-gravimetric (TG) and differential thermal analysis (DTA) were carried out study the thermal stability of the resulting composites. The nano- composites were weakly ferromagnetic at room temperature. Formation of conducting emeraldine salt form was concluded by electrical conductivity.
以过硫酸铵为氧化剂,采用界面聚合法制备了聚苯胺(Pani)和聚苯胺- co3o4纳米复合材料。利用傅里叶变换红外光谱(FTIR)和x射线衍射(XRD)技术研究了规则纳米复合材料的形成。采用扫描电镜(SEM)和透射电镜(TEM)对其形貌进行表征。通过热重分析(TG)和差热分析(DTA)研究了复合材料的热稳定性。纳米复合材料在室温下具有弱铁磁性。通过电导率分析,得出了导电绿宝石盐形态的形成。
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引用次数: 41
Ferroelectric Relaxor Behavior and Spectroscopic Properties of Ba 2+ and Zr 4+ Modified Sodium Bismuth Titanate ba2 +和zr4 +改性钛酸铋钠的铁电弛豫行为和光谱性质
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120204.03
B. Tilak
Polycrystalline ceramics (Na0.5 Bi0.5)1-xBax ZryTi1-yO3, (BNBZT) (for x=0.10, 0.12; y=0.04), has been synthe- sized by conventional solid-state sintering. X-ray diffraction analysis indicates the formation of a single phase with tetragonal symmetry with pure perovskite structure. Scanning electron micrograph of the studied materials shows a distribution of grains. A broad dielectric peak with maximum permittivity has been observed near 1200 (for x=0.10, y=0.04) and 1600 (for x=0.12, y=0.04) respectively in the temperature range, RT-600℃. This result indicates that these materials may have great potential for a variety of high temperature applications. These ceramics show diffuse phase transition and the transition temperature shifting toward higher temperature with increasing frequency, which represents the relaxor behvaiour. The relaxor materials obey modified Curie-Weiss law and Vogel-Fulcher relationship. The values of the diffuseness parameter γ=2 for x = 0.10 and 1.67 for x = 0.12, obtained from the fit of a modified Curie-Weiss law established the relaxor type nature. For a more detailed interpretation of the ac data, the complex impedance (Z*) and electric modulus (M*) as a function of frequency f (i.e., 45 Hz-5 MHz) has been simultaneously analysed. Impedance study reveals that there exists a temperature dependent electrical relaxation phenomenon in the materials. Modulus represents hopping of ions and localized motion in studied compositions. Conductivity obey's Jonscher law
多晶陶瓷(Na0.5 Bi0.5)1-xBax ZryTi1-yO3, (BNBZT)(对于x=0.10, 0.12;Y =0.04),采用传统的固相烧结方法合成。x射线衍射分析表明形成了具有纯钙钛矿结构的四方对称单相。所研究材料的扫描电镜显示了晶粒的分布。在RT-600℃的温度范围内,在1200 (x=0.10, y=0.04)和1600 (x=0.12, y=0.04)附近分别观察到宽介电峰,最大介电常数。这一结果表明,这些材料在各种高温应用中具有很大的潜力。这些陶瓷表现为弥漫性相变,相变温度随频率的增加而向更高温度移动,表现为弛豫行为。弛豫材料服从修正的居里-魏斯定律和Vogel-Fulcher关系。对修正的居里-魏斯定律拟合得到的扩散参数γ=2 (x = 0.10)和1.67 (x = 0.12)确立了弛豫型性质。为了更详细地解释交流数据,同时分析了复阻抗(Z*)和电模量(M*)作为频率f(即45 Hz-5 MHz)的函数。阻抗研究表明,材料中存在与温度相关的电弛豫现象。模量表示所研究成分中离子的跳跃和局部运动。电导率服从琼舍尔定律
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引用次数: 27
Synthesis of Gold-Palladium Bimetallic Nanoparticles and Surface Catalytic Activity in Suzuki Coupling Reactions Using in FTIR Spectroscopy 金-钯双金属纳米颗粒的合成及其铃木偶联反应的表面催化活性研究
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120203.09
P. Venkatesan, J. Santhanalakshmi
Colloidal bimetallic gold core palladium shell nanoparticles were prepared by wet chemical method, in which Au(III) and Pd(II) ions in an aqueous solution in the presence of a cationic surfactant, Cetyltrimethylammonium bromide (CTAB). The structure and composition of the metallic nanoparticles were characterized by UV-Vis, HRTEM, SEM-EDX, XRD, XPS and FTIR. The catalytic activities of nanoparticles are tested on the surface chemical characterization study of Cetyltrimethylammonium bromide supported Au-Pd bimetallic nanoparticle catalyst, hereafter named Au-Pdnp, is reported. Such a catalyst was developed for the Suzuki coupling reaction and found excellent catalytic activity. Here we describe the catalytic performance and the FTIR studies provide proof of the mode of binding that occurs in the Palladium nanoparticle surface for the first time and also confirms the mechanism of the Suzuki reaction.
采用湿化学方法,将Au(III)和Pd(II)离子置于阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)存在的水溶液中,制备了胶体双金属金核钯壳纳米粒子。采用UV-Vis、HRTEM、SEM-EDX、XRD、XPS和FTIR表征了金属纳米颗粒的结构和组成。对十六烷基三甲基溴化铵负载的Au-Pd双金属纳米颗粒催化剂(以下简称Au-Pdnp)进行了表面化学表征研究,测试了纳米颗粒的催化活性。该催化剂用于Suzuki偶联反应,具有良好的催化活性。本文描述了钯纳米颗粒的催化性能,FTIR研究首次证明了钯纳米颗粒表面的结合模式,并证实了铃木反应的机理。
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引用次数: 4
Band Gap Determination of Copper Doped Tungsten Diselenide Single Crystals by Optical Absorption Method 光吸收法测定铜掺杂二硒化钨单晶带隙
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20110102.25
M. Deshpande, M. N. Parmar, Nilesh N. Pandya, Sandip V. Bhatt, S. Chaki
Absorption spectrum of copper (Cu) doped WSe2 (% of Cu = 0.0, 0.5, 1.0) single crystals were obtained in the range 700 nm to 1450 nm. The energy gap and phonon energies were determined for the crystals from the spectrum using two and three dimensional models. This study reflects that indirect transition is dominant in these crystals. On the basis of three dimensional models it was not possible for us to decide whether the indirect inter-band transition is forbidden or allowed type. Hence, different plots were made for two dimensional models, which showed that indirect forbidden transition holds accu- rately for this sample whereas indirect allowed type transition is not valid. The phonon energies calculated for these samples corresponds to the energies associated with optical phonons. The obtained results are discussed in details in this paper.
在700 ~ 1450 nm范围内获得了铜(Cu)掺杂WSe2 (% of Cu = 0.0, 0.5, 1.0)单晶的吸收光谱。利用二维和三维模型从光谱中确定了晶体的能隙和声子能量。本研究反映了这些晶体以间接转变为主。在三维模型的基础上,我们无法确定间接带间跃迁是禁止型还是允许型。因此,对二维模型进行了不同的绘制,结果表明间接禁止型转换对该样本有效,而间接允许型转换无效。为这些样品计算的声子能量与光学声子的能量相对应。本文对所得结果进行了详细的讨论。
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引用次数: 3
Electricalconductivity and Dielectric Properties of Bi 0.5 (Na 0.7 K 0.2 Li 0.1 ) 0.5 TiO 3 Ceramic Material Bi 0.5 (Na 0.7 K 0.2 Li 0.1) 0.5 tio3陶瓷材料的电导率和介电性能
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120202.04
K. Ch.Varada Rajulu, Tilak B, K. Sambasiva Rao
Solid state reaction route is used by adopting calcination, dry pressing and sintering for the preparation of polycrystalline Bi0.5(Na0.7K0.2Li0.1)0.5 TiO3(BNKLT) material. Studies of dielectric and conductivity parameters of the ma- terial were studied as a function of frequency(45Hz to 5MHz) and temperature(RT-600℃). At higher temperatures the conductivity curves were found to be merging, due to the effect of release of space charge.The conductivity parameters such as ion-hopping rate (ωp), fitting parameters (n(T), A(T)) and the charge carrier concentration(K ' ) terms have been calculated using Almond and West formalism.A strong dispersion in both the components of complex dielectric constant, appear to be a common feature in ferroelectrics associated with good ionic conductivity and is referred to as the low frequency dielectric dispersion(LFDD).This offered an opportunity to obtain a good candidate for replacing the lead based ceramics.
采用煅烧、干压、烧结等固相反应途径制备了Bi0.5(Na0.7K0.2Li0.1)0.5 TiO3(BNKLT)多晶材料。研究了材料的介电和电导率参数随频率(45Hz ~ 5MHz)和温度(RT-600℃)的变化规律。在较高的温度下,由于空间电荷释放的影响,电导率曲线趋于合并。利用Almond和West的形式化方法计算了离子跳变率(ωp)、拟合参数(n(T)、A(T))和载流子浓度(K’)等电导率参数。复合介电常数两个分量的强色散,似乎是与良好离子电导率相关的铁电体的共同特征,被称为低频介电色散(LFDD)。这为获得替代铅基陶瓷的良好候选材料提供了机会。
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引用次数: 10
On the Primary Phase Microstructure of Solidifying Ti-46Al-8Nb Refractory Intermetallic Alloy Ti-46Al-8Nb难熔金属间合金凝固初相组织研究
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120202.06
A. Kartavykh
The reported contradictory data on microstructure formation of the refractory intermetallic Ti-46Al-8Nb (at.%) alloy and on the high-temperature phase transformations proceeding within the Ti-Al-Nb phase diagram are ana- lysed and clarified experimentally. To determine the primary solidifying phase, a set of experiments is performed on melt- ing of the alloy specimens with low oxygen contamination in a high purity argon atmosphere using crucibles made of oxy- gen-free ceramics (99.99% AlN), and subsequent rapid solidification. Volumetrically-isothermal cooling from 1943 K at rates of 5, 10, and 20 K/s and following quench of mini-ingots from 1763 K are used. Specimens were studied by scanning electron microscopy (SEM) in backscattered electron (BSE) mode. SEM-BSE micrographs demonstrate contrasting shadow regions of non-uniform niobium segregation, which are fixed by quench and decorate the primary polycrystalline microstructure formed within the temperature range between 1843 (liquidus) and 1773 K (solidus). The primary crystalliz- ing phase is proven to be represented by β(Ti) dendrites, which have clearly pronounced fourfold (bcc-lattice) symmetry being formed with secondary dendrite arms development. The solidification path is shown to be described with single- phase scheme L→L+β(Ti)→β(Ti); no peritectic β(Ti)→α(Ti) bcc-hcp phase transformation revealed within the mushy state of alloy.
本文通过实验分析和澄清了有关难熔Ti-46Al-8Nb (at.%)合金显微组织形成与Ti-Al-Nb相图内高温相变过程的矛盾数据。为了确定合金初次凝固相,采用无氧陶瓷(99.99% AlN)坩埚在高纯氩气气氛中对低氧污染合金试样进行了熔炼和快速凝固实验。体积等温冷却从1943 K在5,10和20 K/s的速率和随后的淬火迷你锭从1763 K使用。采用背散射电子(BSE)模式对样品进行扫描电镜(SEM)研究。SEM-BSE显微图显示,在1843 K(液相线)和1773 K(固相线)温度范围内形成的初生多晶微观结构中,铌偏析的阴影区被淬火固定和修饰。初生晶相以β(Ti)枝晶为代表,具有明显的四重(bcc-晶格)对称,伴随二次枝晶臂的发育。凝固路径为L→L+β(Ti)→β(Ti);糊状合金中未出现包晶β(Ti)→α(Ti) bcc-hcp相变。
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引用次数: 4
Evolution of Structure, Microstructure, Electrical and Magnetic Properties of Nickel Oxide (NiO) with Transition Metal ion Doping 过渡金属离子掺杂氧化镍(NiO)的结构、微观结构、电性能和磁性能演变
Pub Date : 2012-08-31 DOI: 10.5923/J.MATERIALS.20120203.06
P. Mallick, N. Mishra
We present a brief review on the evolution of structure, microstructure, electrical and magnetic properties of NiO with transition metal (TM) doping. The fcc structure of NiO is not affected with TM doping whereas the some of the TM ion influences the microstructure. The antiferromagnetic property of NiO is strongly modified with some of the TM (Fe, Mn, V) doping and the same is not much affected with some other TM (Co, Cr, Zn and Cu) doping. Not only the dopants but also the form of the material decides the magnetic order in the host matrix. Powder NiO exhibits room tem- perature ferromagnetism with Fe doping, superparamagnetism with Mn doping. NiO thin films on the other hand exhibit ferromagnetism with Fe, Mn and V doping. The ferromagnetic ordering in these cases was improved with Li co-doping. The increased ferromagnetism in these cases may be due to increase of hole concentration due to Li doping. Giant dielectric response has been observed for (Li, Fe) and (Li, V) doped NiO ceramics.
本文综述了过渡金属(TM)掺杂后NiO的结构、微观结构、电学和磁学性能的演变。TM不影响NiO的fcc结构,但部分TM离子对其微观结构有影响。某些TM (Fe, Mn, V)掺杂对NiO的反铁磁性能有较强的影响,而其他TM (Co, Cr, Zn, Cu)掺杂对NiO的反铁磁性能影响不大。掺杂剂和材料的形态决定了基体的磁序。Fe掺杂的NiO粉末具有室温铁磁性,Mn掺杂的NiO粉末具有超顺磁性。另一方面,掺杂Fe、Mn和V的NiO薄膜表现出铁磁性。在这些情况下,Li共掺杂改善了铁磁有序性。在这些情况下,铁磁性的增加可能是由于Li掺杂增加了空穴浓度。在(Li, Fe)和(Li, V)掺杂的NiO陶瓷中观察到巨大的介电响应。
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引用次数: 44
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