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At least 271 records · Page 15

Sticking-Free Reduction of Titanomagnetite Ironsand in a Fluidized Bed Reactor

Fluidized bed reduction of iron ore fines is typically inhibited by the onset of “sticking” at temperatures above 973 K, which leads to particle agglomeration and defluidization of the bed. Here, we report the sticking-free fluidized bed reduction of titanomagnetite (TTM) ironsand at 1223 K in Ar-H{sub 2} gas mixtures. We show that sticking is prevented by the formation of a protective titanium-rich oxide shell around each particle during the initial reduction stage. This protective shell prevents iron-iron contact between particles throughout the reduction process, enabling metallization degrees of 93 pct to be attained without sticking occurring. Phase evolution during the reaction has also been analyzed using q-X-ray diffraction and scanning electron microscope/energy dispersed spectroscopy. We find that the reduction proceeds through four separate stages. During the initial stage, approximately half of the initial TTM phase is converted to wüstite, forming a network of sub-micron wüstite channels which interlace the TTM matrix. During this stage, Ti and Al are enriched within the TTM matrix, due to the low solubility of both species in wüstite. This enrichment stabilizes the remaining TTM, meaning that wüstite is then preferentially reduced to metallic iron in stage 2 of the reduction. In stage 3, the remaining Ti-enriched TTM is reduced directly to metallic iron and ilmenite. The final stage of reduction involves the conversion of ilmenite into rutile and pseudobrookite. Our findings clarify the important role played by titanium species during the reduction of TTM and suggest that New Zealand ironsand can offer significant advantages over conventional hematite ores when used as a feedstock for fluidized bed direct-reduced iron processes.

36 MATERIALS SCIENCE↗

Effect of Ca and Sm Combined Addition on the Microstructure and Elevated-Temperature Mechanical Properties of Mg-6Al Alloys

In the present study, the microstructure and elevated-temperature mechanical properties of Mg-6Al, Mg-6Al-4Ca, Mg-6Al-4Sm and Mg-6Al-2Ca-2Sm alloys were investigated. The experimental results showed that the microstructure and elevated-temperature mechanical property of Mg-6Al alloy changed obviously with the different elements addition. By analyzing the results of optical microscope, x-ray diffraction analysis, scanning electron microscope, and transmission electron microscope, it could be determined that there was only Mg{sub 17}Al{sub 12} phase in Mg-6Al alloy, there were Al{sub 2}Ca and (Mg, Al){sub 2}Ca phases in Mg-6Al-4Ca alloy, there were Al{sub 2}Sm and Mg{sub 17}Al{sub 12} phases in Mg-6Al-4Sm alloy, and there were (Mg, Al){sub 2}Ca, Al{sub 2}Ca and Al{sub 2}Sm phases in Mg-6Al-2Ca-2Sm alloy. In addition, the addition of alloying elements including Ca and Sm, especially the composite addition, could significantly improve the tensile properties of Mg-6Al alloy. Compared to Mg-6Al alloy, the tensile strengths of Mg-6Al-2Ca-2Sm alloy at 448, 473 and 498 K were enhanced by 50.32, 87.92, and 94.99%, respectively. Furthermore, when the stretching temperatures were 448 and 473 K, the fracture pattern of Mg-6Al-2Ca-2Sm alloy was the mixture of intergranular fracture and trans-crystalline fracture. However, when the stretching temperature was 498 K, the fracture pattern of Mg-6Al-2Ca-2Sm alloy was the intergranular fracture.

36 MATERIALS SCIENCE↗

Pure and cerium-doped zinc orthosilicate as a pigment for thermoregulating coatings

Microwave-assisted hydrothermal synthesis followed by high-temperature (1050 °C) calcination was used to prepare pure and cerium-doped zinc orthosilicate (Zn 2 SiO 4 ) pigments. Nanoscale Zn 2 SiO 4 and Ce–Zn 2 SiO 4 powders were blended with potassium silicate (K 2 SiO 3 ) and then applied to the aluminum substrate to obtain thermoregulating coatings. Electron beams with different energies were used to irradiate nanoscale pigment powders and coatings. X-ray diffraction (XRD), scanning electron microscopy (SEM), and transition electron microscopy (TEM) were used to characterize the phase composition, morphology, and atomic-level structure of materials. Here, the diffuse reflectance and absorption measurements of materials before and after irradiation indicated that Ce–Zn 2 SiO 4 -based coatings exhibit better radiation resistance compared to pure Zn 2 SiO 4 . Simple and straightforward preparation, as well as high radiation resistance, make Ce–Zn 2 SiO 4 -based thermoregulating coatings excellent candidates for space vehicles.

36 MATERIALS SCIENCE↗

New insights on the formation of supersaturated Cu-Nb solid solution prepared by mechanical alloying

The deformation-driven alloying mechanisms in the immiscible Cu-Nb system during mechanical alloying (MA) process have been studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) observations. It is found that the dominating alloying mechanism changes at the different stages of milling. Initially, the alloying process is mainly governed by interfaces and dislocations, which supply fast diffusion channels between phases. In the intermediate stage, Nb particles with sizes below 8 nm undergo a bcc to fcc allotropic transformation, and the interdiffusion between fcc-Nb and fcc-Cu is promoted due to the similarity of lattice structures. Further milling generates disclination defects, which contribute to the formation of fragments or subgrains with sizes below 5 nm. The introduction of such defects and fragments benefits the formation of a complete Cu-Nb solid solution. The formation kinetics of solid solution is analyzed by Johnson-Mehl-Avrami equation, which suggests that the speed of the diffusion of Nb atoms into Cu is very slow. - Highlights: •The bcc to fcc transformation in Nb nanoparticles promotes diffusion process. •The formation of fragments with sizes below 5 nm is attributed to the disclination defects. •Defect-assisted diffusion is responsible for the alloying process.

36 MATERIALS SCIENCE↗

Microstructure and nanoindentation analysis of Mg-SiC nanocomposite powders synthesized by mechanical milling

Highlights: • Mechanical milling as an effective solution to reach a homogeneous distribution of SiC nanoparticles up to 10 vol% in Mg matrix • No deformation twinning in the nanostructured Mg matrix even after the severe plastic deformation and hard SiC nanoparticles up to 10 vol%. • Significant enhancement of nanohardness and reduced elastic modulus in the milled nanocomposite powders - Abstract: Mixtures of magnesium powder and SiC nanoparticles at various volume fractions were mechanically milled to produce nanocrystalline Mg-SiC nanocomposites. X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were utilized to characterize the microstructure of the milled powders. The microstructural evidences revealed that mechanical milling is a proper method to achieve a uniform distribution of the SiC nanoparticles, even up to 10% in the Mg matrix. Based on the results, higher volume fraction of the SiC nanoparticles raise the value of measured microstrain and reduce the crystallite size of the Mg matrix. The TEM results pointed to the fact that no deformation twinning takes place in the nanostructured Mg matrix even after severe plastic deformation through mechanical milling and the presence of hard SiC nanoparticles up to 10 vol%. The effects of nanoparticle volume fraction on mechanical properties of the milled Mg-SiC nanocomposites were evaluated using nanoindentation tests. The results clearly showed a significant enhancement of nanohardness and reduced elastic modulus in the milled powders compared to that of the reference material namely as-received pure magnesium. It was found that the SiC nanoparticles (even up to 10 vol%), well distributed in the magnesium matrix, remarkably improve the reduced elastic modulus and nanohardness of the nanocomposite powders.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Synthesis and behaviors of g-C3N4 coupled with LaxCo3-xO4 nanocomposite for improved photocatalytic activeity and stability under visible light

Novel La{sub x}Co{sub 3-x}O{sub 4} doped graphitic carbon nitride photocatalysts were synthesized via a microwave-assisted hydrothermal method. The rate of H{sub 2} production varies with the ratio of the La/Co doped on g-C{sub 3}N{sub 4}, the highest hydrogen production activity is 63.12 μmol h{sup −1} when the molar ratio of La/Co is 10% in the nanohybrid. The nanohybrid photocatalyst exhibited activity for hydrogen generation is higher than that of pure g-C{sub 3}N{sub 4} by up to 6 times under visible light irradiation. The synergistic effect of g-C{sub 3}N{sub 4} and La{sub x}Co{sub 3-x}O{sub 4} leads to efficient separation of the photogenerated charge carriers, as a result of enhances the visible light photocatalytic hydrogen production activity of the photocatalysts. The effective coupling of La{sub x}Co{sub 3-x}O{sub 4} on g-C{sub 3}N{sub 4} can efficiently extend the light absorption of the g-C{sub 3}N{sub 4} to visible region and enhance the charge separation efficiency of g-C{sub 3}N{sub 4}/La{sub x}Co{sub 3-x}O{sub 4} composites. The possible photocatalytic mechanism of the g-C{sub 3}N{sub 4}/La{sub x}Co{sub 3-x}O{sub 4} photocatalysts is inferred by XPS, X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), photoluminescence spectroscopy (PL), and electrochemical workstation.

36 MATERIALS SCIENCE↗

Surface phases of the transition-metal dichalcogenide IrTe 2

Transition-metal dichalcogenide IrTe 2 has attracted attention because of its striped lattice, charge ordering, and superconductivity. We have investigated the surface structure of IrTe 2 , using low-energy electron diffraction and scanning tunneling microscopy. A complex striped lattice modulation as a function of temperature is observed, which shows hysteresis between cooling and warming. While the bulk 5 × 1 and 8 × 1 phases appear at high temperatures, the surface ground state has the 6 × 1 phase, not seen in the bulk, and the surface transition temperatures are distinct from the bulk. Here, the broken symmetry at the surface creates a quite different phase diagram, with the coexistence of several periodicities resembling devil's staircase behavior.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Optimization of the CVD parameters for ZnO nanorods growth: Its photoluminescence and field emission properties

Highlights: • Home-made CVD reactor fabricated and successfully used for growing ZnO nanorods. • Growth of nanostructures depends on several CVD process parameters. • CVD parameters, flow rate of carrier gas, substrate temperature, Au catalyst droplet size, growth time duration, etc. optimized. • The mechanism of crystal growth understood by studying FESEM/TEM/XRD. • Photoluminescence and Field emission studies done for defects and applications. - Abstract: Vertically aligned single crystalline ZnO nanorods arrays were grown on a silicon substrate in a CVD reactor using Au as a catalyst. The CVD parameters such as substrate temperature, catalyst layer thickness/morphology and reaction time play a crucial role in the synthesis of nanostructures by the vapor-liquid-solid process. By optimizing these various CVD parameters, highly controlled guided growth of ZnO nanorods was achieved. The structural and morphological properties of resultant ZnO nanorods were studied by means of X-ray diffraction, high-resolution transmission electron microscopy, selected area electron diffraction and field emission scanning electron microscopy. The photoluminescence spectroscopy was also done to investigate the defects in grown ZnO nanorods. The field emission results of nanorods array indicated that the properties of the field emission follow Fowler–Nordheim law. The nanorods (grown for 20 min) are vertically aligned on the substrate surface without entanglements and with good crystal quality as well which is very important for several applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Orientation Behavior and Mechanism of Ag-doped GdBa2Cu3O7-δ Superconducting thin Films Derived by Metal Organic Deposition

Ag-doped GdBa{sub 2}Cu{sub 3}O{sub 7−δ} (GdBCO)-coated conductors are fabricated via a metal-organic process. The X-ray diffraction and scanning electron microscopy results show that the growth conditions of the GdBa{sub 2}Cu{sub 3}O{sub 7−δ} matrix are modified, resulting in less a-axis growth and much smoother surface morphology and finally giving rise to much improvement of superconducting performance in a wide range of processing parameters. The orientation behavior and mechanism of Ag-doped GdBCO films are investigated. To reasonably explain the orientation behavior of Ag-doped GdBCO films, a simple nucleation model for Ag-doped GdBCO is established, suggesting quasi-liquid phases are perfected by Ag. As a consequence, a-axis nucleation is suppressed and strong c-axis nucleation is achieved in a wider processing window.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Structure, Morphology, Cation Distribution and Magnetic Properties of Cr{sup 3+}-Substituted CoFe{sub 2}O{sub 4} Nanoparticles

The present investigations deal with the effect of trivalent chromium ions (Cr{sup 3+}) on structural and magnetic properties of nanocrystalline cobalt ferrite (CoFe{sub 2}O{sub 4}) nanoparticles. The samples of CoCr{sub x}Fe{sub 2−x}O{sub 4} (where x = 0.0 to 1.0 in step of 0.2) were successfully synthesized by citric acid-assisted sol-gel auto combustion method. Further, the prepared samples were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), infrared spectroscopy (IR) and pulsed field hysteresis loop technique for structural, morphological and magnetic properties analysis, respectively. XRD patterns showed the formation of single-phase cubic spinel structure with broad Bragg’s peak for all the samples. The value of lattice parameter was found to be decreased with chromium substitution x. Cation distribution studies revealed that Co{sup 2+} and Fe{sup 3+} occupied both A and B sites, whereas Cr{sup 3+} ions occupied only B site. SEM analysis of the prepared samples confirmed the nanocrystalline nature of the material. The two absorption bands belonging to spinel structure were observed in IR spectra. Saturation magnetization (M{sub S}), remanence magnetization (M{sub r}) and coercivity (H{sub C}) was found to be decreased with increase in chromium substitution x.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Performance efficiency and kinetic studies of water purification using ZnO and MgO nanoparticles for potassium permanganate

Zinc oxide (ZnO) and Magnesium oxide (MgO) nanoparticles (NPs) have been synthesized by solid–solid reaction technique. X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier-transform infrared (FTIR) were used to investigate the structural properties of ZnO and MgO NPs. XRD indicates that structural of ZnO NPs has a hexagonal structure with space group P63mc. On the other hand, MgO NPs is cubic structure with space group Fm 3-bar m. The photocatalytic efficiency of both ZnO and MgO NPs as a catalyst was illustrated by studying the extreme quantity of potassium permanganate (KMnO{sub 4}) degradation rate in wastewater. KMnO{sub 4} achieved 17% and 25% degradation rate in 180 min for ZnO and MgO NPs, respectively. The experimental data were examined by the kinetic models of pseudo-first and second order as well as intra-particle diffusion. The obtained data is expressed well by the second-order kinetic model for both NPs. Moreover, according to the experimental results, MgO NPs has high-performance water purification as a comparison of ZnO NPs effect.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Processing and Characterization of Fe-Mn-Cu-Sn-C Alloys Prepared by Ball Milling and Spark Plasma Sintering

In this work, Fe-Mn-Cu-Sn-C alloys were prepared by means of powder metallurgy (PM). Powder mixtures were ball-milled for 8, 30 and 120 h and densified to < 1% porosity using spark plasma sintering (SPS) at 900 °C and 35 MPa. After consolidation, all samples of the Fe alloys were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), hardness and flexural strength tests. Resistance to abrasive wear was evaluated in both three-body abrasion and two-body abrasion tests. The SEM observations revealed an evident dependence of grain size and microstructural homogeneity on milling time. The XRD analysis showed a marked increase in austenite content in the as-sintered specimens with milling time. Although the proportion of deformation-induced martensite was small, the strengthening effect of abrasion on the subsurface layer of the investigated alloys was clearly indicated by Knoop hardness measurements.

36 MATERIALS SCIENCE↗

Size and morphology controlled NiSe nanoparticles as efficient catalyst for the reduction reactions

Facile and efficient ball milling and polyol methods were employed for the synthesis of nickel selenide (NiSe) nanoparticle. The particle size of the NiSe nanoparticle has been controlled mechanically by varying the ball size in the milling process. The role of the surfactants in the formation of various morphologies was studied. The compounds were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray energy dispersive spectroscopy (EDS). The efficiency of the NiSe nanoparticle as a catalyst was tested for the reduction of para-nitroaniline (PNA) to para-phenyldiamine (PPD) and para-nitrophenol (PNP) to para-aminophenol (PAP) using NaBH{sub 4} as the reducing agent. Particle size, morphology and the presence of surfactant played a crucial role in the reduction process. - Graphical abstract: NiSe nanoparticles in different size and morphology were synthesized using facile ball milling and polyol methods. Particle size, morphology and the presence of surfactant in these materials played a crucial role in the hydrogenation of PNA and PNP. - Highlights: • NiSe nanoparticles synthesized using ball milling and solution phase methods. • NiSe nanoparticle is an efficient catalyst for the reduction of PNA and PNP. • NiSe is found to be better than the best reported noble metal catalysts.

36 MATERIALS SCIENCE↗

Microstructural evolution and grain growth kinetics of GZ31 magnesium alloy

Grain growth behavior of Mg–3Gd–1Zn (GZ31) magnesium alloy was studied in a wide range of annealing time and temperature to clarify the kinetics of grain growth, microstructural evolution and related metallurgical phenomena. This material exhibited typical normal grain growth mode under annealing conditions with annealing temperature of lower than 300 °C and soaking time of lower than 240 min. However, the abnormality in grain growth was also evident at annealing temperature of 400 °C and 500 °C. The dependence of abnormal grain growth (AGG) at mentioned annealing temperatures upon microstructural features such as dispersed precipitates, which were rich in Zn and Gd, was investigated by optical micrographs, X-ray diffraction patterns, scanning electron microscopy images, and energy dispersive X-ray analysis spectra. The bimodality in grain-size distribution histograms also signified the occurrence of AGG. Based on the experimental data on grain growth obtained by annealing treatments, the grain growth exponent and the activation energy were also figured out.

36 MATERIALS SCIENCE↗

Effect of Ce addition on the microstructure and properties of Al-Cu-Mn-Mg-Fe lithium battery shell alloy

Highlights: • Al{sub 6}(Mn, Fe) particles could be remarkably refined by Ce alloying. • Ce addition to the alloy promoted precipitation of S' phase. • Ce-containing alloy had higher tensile strength than that of Ce-free alloy. • Ce-containing alloy had positive corrosion potential and lower corrosion current density. - Abstract: Effect of Ce addition on the microstructures, mechanical properties and electrochemical properties of Al-Cu-Mn-Mg-Fe lithium battery alloy was investigated by optical microscope (OM), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), tensile testing and electrochemical testing. Experimental results indicate that Ce addition resulted in the formation of Al{sub 8}Cu{sub 4}Ce phase in the Al-Cu-Mn-Mg-Fe alloy. The Ce-containing precipitates nucleated and grew up along the surface of Al{sub 6}(Mn, Fe) precipitates. Al{sub 6}(Mn, Fe) precipitates could be remarkably refined by Ce alloying. The aging precipitation behavior of S' phases could be promoted after Ce addition to the alloy. In comparison with Ce-free alloy, the Ce-containing alloy had higher tensile strength at both low temperature and elevated temperature. Especially at 200 °C, the yield strength and tensile strength of Ce-containing alloy substantially increased by 23.4% and 27.08%, respectively. Potentiodynamic polarization testing indicated that the Ce-containing alloy had a more positive corrosion potential and a lower corrosion current density.

36 MATERIALS SCIENCE↗

Fabrication of Biodegradable Superabsorbent Using RSM Design for Controlled Release of KNO{sub 3}

Present study envisaged the sequential experimental design approach for the development of biodegradable Gelatin-Tapoica/polyacrylamide superabsorbent. Percentage water uptake efficacy of candidate sample was optimized using Response Surface Methodology (RSM) design under microwave irradiation. Different process variables such as potassium persulphate and ammonium persulphate (KPS:APS) ratio, pH, reaction time concentration of acrylamide and N,N-methylene-bis-acrylamide (MBA) were investigated as a function of percentage swelling using sequential experimental design. Maximum liquid efficacy of 1550% was obtained at KPS:APS = 1.0:0.5; acrylamide = 7.67 × 10{sup −1} mol L{sup −1}; MBA = 1.76 × 10{sup −2} mol L{sup −1}; pH 10 and time = 110 s. The 3D crosslinked network formed was characterized using Fourier Transformation Infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscopic (SEM) techniques and thermal stability was ensured by Thermal gravimetric Analysis/Differential Thermal Analysis/Differential Thermal Gravimetric (TGA/DTA/DTG) studies. Superabsorbent synthesized could increase the moisture content in different type of soils and was found to enhance the water-holding capability of the soil upto 60 days in clayey, 40 days in sandy and 51 days in mixture of two soils under controlled conditions. Further, candidate polymer was investigated for the in-vitro controlled release of the KNO{sub 3} with diffusion exponent ‘n’ was found to be 0.4326 indicating Fickian type diffusion. Also, initial diffusion coefficient (D{sub I} = 3.49 × 10{sup −5} m{sup 2} h{sup −1}) was found to be greater than the lateral diffusion coefficient (D{sub L} = 3.76 × 10{sup −6} m{sup 2} h{sup −1}) indicated rapid release of KNO{sub 3} during initial hours with slow release afterwards. The ecofriendly nature of the synthesized polymer was also tested by conducting biodegradation studies and it was found to degrade upto 94% and 88.1% within 70 days with degradation rate of 1.34 and 1.26% per day using composting method and vermicomposting method respectively. So, the synthesized candidate polymer was found to be boon for agriculture-horticulture sector with wide applicability.

36 MATERIALS SCIENCE↗

Investigation of Microstructural and Magnetic Properties of BaV{sub x}Fe{sub 12−x}O{sub 19} Nanohexaferrites

Nanohexaferrites of BaV{sub x}Fe{sub 12−x}O{sub 19} (0.0 ≤ x ≤ 0.1) were prepared using sol–gel auto-combustion. The structure and morphology of BaV{sub x}Fe{sub 12−x}O{sub 19} (0.0 ≤ x ≤ 0.1) nano-sized hexaferrites were explored by X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with EDXS. XRD analysis indicated particle size in the 55–60-nm interval. SEM and EDXS investigations confirmed the formation of the desired composition of V-substituted Ba-hexaferrites. The magnetic properties of products were studied. The magnetic M(H) hysteresis loops revealed that all produced nanohexaferrites display ferromagnetic-like comportment. The deduced saturation magnetization (M{sub s}), retentivity (M{sub r}), magneto-crystalline anisotropy fields (H{sub a}), and coercive field (H{sub c}) were enhanced for low V{sup 3+} contents and were maximum for BaV{sub 0.04}Fe{sub 11.96}O{sub 19} (x = 0.04) nanohexaferrites, showing the strengthening of magnetic properties.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

AC Magnetic Susceptibility of Y{sub 3}Ba{sub 5}Cu{sub 8}O{sub 18} Substituted by Nd{sup 3+} and Ca{sup 2+} Ions

Effect of Nd{sup 3+} and Ca{sup 2+} ion substitutions in Y{sub 3}Ba{sub 5}Cu{sub 8}O{sub 18} (Y-358) was studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), electrical resistivity, and ac magnetic susceptibility measurements. Superconducting samples of type Y{sub 3 − x}Nd{sub x}Ba{sub 5 − y}Ca{sub y}Cu{sub 8}O{sub 18} (with 0 ≤ x, y ≤ 0.4) were synthesized by the standard solid-state reaction technique. XRD patterns revealed that all the samples were mainly composed of Y-358 phase with orthorhombic structure. SEM micrographs showed that Nd{sup 3+} and Ca{sup 2+} ion substitutions had the ability to alter the grain morphology of Y-358 to irregular randomly oriented grains with smaller average grain sizes. The temperature-dependent electrical resistivity curves indicated that the superconducting transition temperature T{sub c} was decreased from 96.51 to 87.41 K as the substitution contents were increased from 0 to 0.4. Detailed AC magnetic susceptibility measurements were done using a quantum design physical property measurement system (PPMS) at different dc fields (B = 0.5–20 kG) and frequency of 1 kHz. A comparison between electrical resistivity and AC magnetic susceptibility data was performed. It was found that T{sub cs} obtained from AC magnetic susceptibility were much lower than those obtained from the resistivity measurements, for all studied samples. This was discussed in terms of filamentary paths that could produce sharp pronounced drops in diamagnetism. Generally, the depression in T{sub c} was attributed to the decrease in relative volume fraction of Y-358 or due to trapping of mobile holes or other mechanism connected with oxygen vacancy disorder. Werthamer–Helfand–Hohenberg (WHH) theory was employed to study the temperature dependence of the upper critical magnetic field B{sub c2}(T) for the samples. The relative importance of both orbital and paramagnetic effects in the suppression of superconductivity was described with the aid of Maki parameter (κ{sub M}). The estimated values of the upper critical magnetic field at 0 K, B{sub c2}(0), were found to decrease from 37.3 to 13.5 T as Nd{sup 3+} and Ca{sup 2+} contents were increased from 0 to 0.4. This decrement was attributed to the weak electron–phonon coupling and to the orbital as well as spin pair breaking mechanisms. Furthermore, Ginzburg–Landau coherence length ξ{sub GL} of Y{sub 3 − x}Nd{sub x}Ba{sub 5 − y}Ca{sub y}Cu{sub 8}O{sub 18} was found to increase with the increase of the Nd{sup 3+} and Ca{sup 2+} contents. Therefore, Nd{sup 3+} and Ca{sup 2+} ions play an important role in the pair-breaking mechanism and in suppressing superconductivity of the Y-358 phase.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗