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排序方式: 共有944条查询结果,搜索用时 15 毫秒
1.
Gui-Jia Gao Mei-Qi Zeng En-Liang Zhang Rong-Chang Zeng Lan-Yue Cui Dao-kui Xu Feng-Qin Wang M.Bobby Kannan 《材料科学技术学报》2021,83(24):161-178
The microstructure and chemical compositions of the solid solution-treated Mg-3Nd-1Li-0.2Zn alloy were characterized using optical microscope,scanning electron microscope(SEM),transmission electron microscope(TEM),electron probe micro-analyzer(EPMA)and X-ray photoelectron spectroscopy(XPS).The corrosion behaviour of the alloy was investigated via electrochemical polarization,electrochemical impedance spectroscopy(EIS),hydrogen evolution test and scanning Kelvin probe(SKP).The results showed that the microstructure of the as-extruded Mg-3Nd-1Li-0.2Zn alloy contained α-Mg matrix and nanometric second phase Mg41 Nd5.The grain size of the alloy increased significantly with the increase in the heat-treatment duration,whereas the volume fraction of the second phase decreased after the solid solution treatment.The surface film was composed of oxides(Nd2O3,MgO,Li2O and ZnO)and carbonates(MgCO3 and Li2CO3),in addition to Nd.The as-extruded alloy exhibited the best corrosion resistance after an initial soaking of 10 min,whereas the alloy with 4h-solution-treatment possessed the lowest corrosion rate after a longer immersion(1 h).This can be attributed to the formation of Nd-containing oxide film on the alloys and a dense corrosion product layer.The dealloying corrosion of the second phase was related to the anodic Mg41Nd5 with a more negative Volta potential relative to α-Mg phase.The preferential corrosion of Mg41Nd5 is proven by in-situ observation and SEM.The solid solution treatment of Mg-3Nd-1Li-0.2Zn alloy led to a shift in corrosion type from pitting corrosion to uniform corrosion under long-term exposure. 相似文献
2.
Xiao-Li Fan Yuan-Fang Huo Chang-Yang Li M.Bobby Kannan Xiao-Bo Chen Shao-Kang Guan Rong-Chang Zeng Quan-Li Ma 《稀有金属(英文版)》2019,(6)
A hexagonal nanosheet Mg(OH)_2 coating was prepared through a one-step hydrothermal method using LiOH solution as mineralizer and then modified by ethylenediaminetetraacetic acid(EDTA) to minimize the rapid corrosion of AZ31 Mg alloy.The performance of the coating was evaluated using electrochemical technique,hydrogen evolution measurements, nanoscratch test,Fourier-transform infrared spectroscopy(FTIR), X-ray diffraction(XRD) patterns and field-emission scanning electron microscopy(FESEM).The results suggested that the corrosion rate of bare AZ31 Mg alloys was significantly reduced by one and two orders of magnitude through the protection from Mg(OH)_2 coating and modification with EDTA(i.e., EDTA-Mg(OH)_2 coating), respectively.FESEM micrographs indicated that the modification in EDTA elicits to the formation of an EDTA-Mg(OH)_2 composite with a thickness as twice as that of as-prepared Mg(OH)_2 coating.Nanoscratch tests revealed strong adhesion between the composite or Mg(OH)_2 coating and the substrate.The study of formation and corrosion mechanisms of the coatings manifested that Mg(OH)_2 was first formed near the intermetallic compound AlMn particles and gradually covered the entire surface, wherein the AlMn particles played an important role in the coating growth process.And it also proved that EDTA accelerated the formation of Mg(OH)_2. 相似文献
3.
Ponnusamy Nandha Kumar Shangavi Subramanian Uthirapathy Vijayalakshmi Sanjeevi Kannan 《Journal of the American Ceramic Society》2020,103(6):3528-3540
Structurally stable β-Ca3(PO4)2/t-ZrO2 composite mixtures with the aid of Dy3+ stabilizer were accomplished at 1500°C. The precursors comprising Ca2+, P5+, Zr4+, and Dy3+ have been varied to obtain five different combinations. The results revealed the fact that complete phase transformation of calcium-deficient apatite to β-Ca3(PO4)2 occurred only at 1300°C, whereas the evidence of t-ZrO2 crystallization is obvious at 900°C. The dual occupancy of Dy3+ at β-Ca3(PO4)2 and t-ZrO2 structures was evident; however, Dy3+ initially prefers to occupy β-Ca3(PO4)2 lattice until its saturation limit and thereafter accommodates at the lattice site of ZrO2. The typical absorption and emission behavior of Dy3+ were noticed in all the systems and, moreover, the surrounding symmetry of Dy3+ domains has been determined from the luminescence study. All the systems ensured paramagnetic response that is generally contributed by the presence of Dy3+. A gradual increment in the phase content of t-ZrO2 in the composite mixtures ensured a significant improvement in the hardness and Young's modulus of the investigated compositions. 相似文献
4.
Kannan K. Thirumalai Rameshbabu S. 《Journal of Mechanical Science and Technology》2018,32(4):1739-1747
Journal of Mechanical Science and Technology - This paper investigates the tribological characteristics of modified jojoba oil (MJO) as a base stoke for SAE20W40 mineral oil (LO). In addition, a... 相似文献
5.
Sharma Nitin Kumar Kannan Rangasayee Li Leijun Anderson Neil Rashid Muhammad Collins Laurie Poplawsky Jonathan D. Unocic Raymond 《Metallurgical and Materials Transactions A》2021,52(9):3788-3798
Metallurgical and Materials Transactions A - The bondline of electric-resistance-welded (ERW) linepipe steel, often etched white (i.e., ferrite) in optical microscopy, is generally believed to be... 相似文献
6.
Kotha Gangadhar Damerla Vijayakumar Ali J. Chamkha Thangavelu Kannan Gnanasekaran Sakthivel 《亚洲传热研究》2020,49(2):838-857
This study article addressesthe flow and heat transfer characteristics of a magnetite Fe3O4 micropolar ferrofluid flow past a stretching sheet. For practical interest, thermal radiation, Newtonian heating, and a heat source or sink are considered in this investigation. A useful Tiwari‐Das nanofluid model is considered to analyze the microstructure and inertial characteristics of the water‐based nanofluids containing iron oxide. The dimensionless nonlinear ordinary differential equations are solved by employing suitable similarity variables. The resulting nonlinear system is solved by the spectral quasi‐linearization method. The effects of different nondimensional parameters on various profiles are shown graphically and explored in detail. It is found that the micropolar ferrofluid exhibits a higher energy distribution than that of a classical micropolar fluid. Compared to the classical micropolar liquid, local skin‐friction is more significant for the micropolar magnetite ferrofluid. In the presence of Newtonian heating, the thermal behavior of the micropolar nanofluid is remarkably better than that of the classical micropolar fluid. 相似文献
7.
8.
Joy Jestin Balakrishnan Kannan Madhavankutty Sreeraj 《Universal Access in the Information Society》2022,21(3):717-723
Universal Access in the Information Society - Lack of Sign Language-based learning tools is a hindrance in acquiring knowledge for deaf students. Technology-based tools have introduced innovative... 相似文献
9.
Synthesis and characterization of poly(ethylene oxide)‐based glycopolymers and their biocompatibility with osteoblast cells 下载免费PDF全文
Mummuluri Trinadh Kannan Govindaraj Tota Rajasekhar Marshal Dhayal Annadanam V Sesha Sainath 《Polymer International》2015,64(6):795-803
Poly(ethylene oxide)‐block‐poly(methacryl‐d ‐glucopyranoside) (PEO‐GP) and poly(methacryl‐d ‐glucopyranoside) (H‐GP) glycopolymers were synthesized by deacetylation of acetylated polymers which were synthesized via atom transfer radical polymerization. The synthesized glycopolymers were characterized using 1H NMR, 13C NMR and Fourier transform infrared (FTIR) spectroscopies, gel permeation chromatography (GPC), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The deacetylated polymers exhibited onset decomposition temperatures about 60 °C lower compared to the polymers having acetyl pendants. The glass transition temperature (Tg) of the acetylated homopolymer was 133 °C and that of the PEO‐based block copolymer was 124 °C. The deacetylated polymers H‐GP and PEO‐GP exhibited Tg values of about ?30 °C. Biocompatibility of the H‐GP and PEO‐GP glycopolymers was obtained by studying osteoblast cell adhesion, viability and proliferation in vitro. The cell viability showed an increase with increasing concentration of H‐GP from 0.1 to 1 µmol L?1 and then decreased with further increase in its concentration (10–1000 µmol L?1). PEO‐GP did not show a significant variation in cell viability on variation of its concentration from 0.1 to 1000 µmol L?1. The significant improvement in biocompatibility with osteoblast cells in the presence of PEO‐GP was considered as due to the covalently bonded PEO segment of the methacrylate glycopolymer block. © 2014 Society of Chemical Industry 相似文献
10.
To quantitatively characterize the substances contributing to estrogenic activity in river water, in vitro bioassay using MVLN cells and instrumental analysis using liquid chromatograph–mass spectrometer (LC/MS) or liquid chromatograph–tandem mass spectrometer (LC/MS/MS) were applied to river water extracts taken from various locations in the Tama River, Japan. Tama River water samples were extracted using solid phase extraction and the crude extracts were fractionated by high-performance liquid chromatography (HPLC) into 10 fractions. The sixth fraction contained nonylphenol (NP) and octylphenol (OP) at concentrations in the range of 51.6–147 and 6.9–81.9 ng/L, respectively (concentrations corresponding to the original sample volumes). No estrogenic activity, expressed as 17β-estradiol equivalents (E2-EQB), however, was observed in this fraction (<0.6 ng-E2eq/L). Instrumentally determined estrogenic activity (E2-EQC), which is the concentrations of NP and OP multiplied by their corresponding relative potency, was below the detection limit of the MVLN cell bioassay. Estrogenic activities were detected only in HPLC fraction nos. 7, 8 and 9. Estrone (E1), estradiol (E2) and bisphenol A (BPA) were detected in these fractions. Estriol (E3) and ethynylestradiol (EE2) were not detected (<0.2 ng/L) in these fractions. The calculated E2-EQC for BPA was below the detection limit of bioassay. The E2-EQC for E1 and E2 were on the same order as the estrogenic activity determined by the bioassay (E2-EQB). The ratios of E2-EQC and E2-EQB for E1 and E2 in the three factions collectively (nos. 7–9) were 0.49–0.97 and 0.29–1.12, respectively. Above results indicated that the major causal substances to the estrogenic activity in the Tama River were E1 and E2. 相似文献