scholarly journals Preparation of La0.7Ca0.3−xSrxMnO3 Manganites by Four Synthesis Methods and Their Influence on the Magnetic Properties and Relative Cooling Power

Materials ◽  
2019 ◽  
Vol 12 (2) ◽  
pp. 309 ◽  
Author(s):  
María Botello-Zubiate ◽  
María Grijalva-Castillo ◽  
Daniel Soto-Parra ◽  
Renee Sáenz-Hernández ◽  
Carlos Santillán-Rodríguez ◽  
...  
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Solid State ◽  
Solid State Reaction ◽  
Pechini Method ◽  
Sol Gel ◽  
Relative Cooling Power ◽  
Cooling Power ◽  
Synthesis Methods ◽  
Consolidation Process

Manganites of the family La0.7Ca0.3−xSrxMnO3 were fabricated by four preparation methods: (a) the microwave-assisted sol-gel Pechini method; (b) sol-gel Pechini chemical synthesis; (c) solid-state reaction with a planetary mill; and (d) solid-state reaction with an attritor mill, in order to study the effect of the preparation route used on its magnetocaloric and magnetic properties. In addition, the manganites manufactured by the Pechini sol-gel method were compacted using Spark Plasma Sintering (SPS) to determine how the consolidation process influences its magnetocaloric properties. The Curie temperatures of manganites prepared by the different methods were determined in ~295 K, with the exception of those prepared by a solid-state reaction with an attritor mill which was 301 K, so there is no correlation between the particle size and the Curie temperature. All samples gave a positive slope in the Arrot plots, which implies that the samples underwent a second order Ferromagnetic (FM)–Paramagnetic (PM) phase transition. Pechini sol-gel manganite presents higher values of Relative Cooling Power (RCP) than the solid-state reaction manganite, because its entropy change curves are smaller, but wider, associated to the particle size obtained by the preparation method. The SPS technique proved to be easier and faster in producing consolidated solids for applications in active magnetic regenerative refrigeration compared with other compaction methods.

Synthesis of Pure Dicalcium Silicate Powder by the Pechini Method and Characterization of Hydrated Cement

2014 ◽  
Vol 787 ◽  
pp. 387-394 ◽  
Author(s):  
Yan Ni Tan ◽  
Yong Liu ◽  
Zhang Qing ◽  
Gurpreet Birdi ◽  
Liam M. Grover
Keyword(s):  
Solid State ◽  
Mass Loss ◽  
Solid State Reaction ◽  
Pechini Method ◽  
Sol Gel ◽  
Dicalcium Silicate ◽  
Hydrated Cement ◽  
Gel Method ◽  
Sol Gel Method

Calcium silicate (CS) is a main component of Portland cement and is responsible for the strength development. Recent research has shown that dicalcium silicate cement (CSC) is bioactive and is a potential candidate for bone replacement. Traditionally, dicalcium silicate powder is synthesized by a solid state reaction or a sol-gel method. The solid-state reaction, however, usually needs a higher temperature and a longer calcination time. Furthermore, the dicalcium silicate powder made by the sol-gel method is not pure, and contains a significant quantity of CaO which is harmful to the strength and biological properties of the CSC. The Pechini technique is an alternative, low temperature polymeric precursor route for synthesis of high purity powders. In this study, purer CS powder was synthesized via the Pechini method by calcination at 800°C for 3h. DSC-TGA, XRD, SEM were used for characterization of CS powder and the hydrated cement. The DSC-TGA curves showed that the main exothermic peak was at 479°C and the total mass loss was 79.2%. The XRD patterns of CSC after hydration for 7, 14, and 35 days illustrated that dicalcium silicate hydrate (Ca1.5SiO3.5·xH2O, C-S-H) was formed in the hardened CS paste. The XRD peaks on the diffraction pattern of the C-S-H of the day 35 sample were of greater intensity than those at day 7 and day 14. This demonstrates that the hydration speed was slow and complete hydration could take more than one month. Flake-like crystals were observed on scanning electron micrographs following hardening. The degradation study result showed that there was no mass loss of CSC after the samples were soaked into phosphate buffered saline (PBS) for 40 days. The silicon assay revealed that orthosilicic acid could be released from CSC after the samples were soaked in simulated body fluid (SBF). Silicon is known to be critical to skeletal mineralization. The existence of silicon may stimulate the proliferation of bone and activate cells to produce bone. Investigation of cell attachment confirmed that the MC-3T3 cells attached well to the surfaces of CSC after seeding.

scholarly journals Structural and Magnetic Properties of Ni0.6Zn0.4Fe2O4Ferrite Prepared by Solid State Reaction and Sol-gel

2014 ◽  
Vol 19 (1) ◽  
pp. 64-67 ◽  
Author(s):  
Yoon Mi Kwon ◽  
Min-Young Lee ◽  
Millaty Mustaqima ◽  
Chunli Liu ◽  
Bo Wha Lee
Keyword(s):  
Magnetic Properties ◽  
Solid State ◽  
Solid State Reaction ◽  
Sol Gel ◽  
Structural And Magnetic Properties

COMPARATIVE STUDY BY SOL-GEL ACRYLAMIDE POLYMERIZATION VIA MICROWAVE AND SOLID STATE SYNTHESIS METHODS IN (Er2-x Srx)Ru2O6 SYSTEM

MRS Advances ◽  
2017 ◽  
Vol 2 (62) ◽  
pp. 3883-3889
Author(s):  
A. Quiroz ◽  
M. Abatal ◽  
E. Chavira ◽  
A. Tejeda ◽  
O. Novel ◽  
...  
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Sol Gel ◽  
Morphological Properties ◽  
Synthesis Methods ◽  
X Ray Diffraction ◽  
Methods Of Synthesis ◽  
Acrylamide Polymerization ◽  
Image Position ◽  
Decomposition Phase

AbstractWe have studied the structural and morphological properties on the pyrochlore (Er2-x Srx)Ru2O6 system, for x = 0.0, 0.02, 0.05, 0.07, 0.10, and 0.15. Polycrystalline samples were prepared by solid-state reaction (SR) and sol-gel acrylamide polymerization (SGAP). Thermogravimetric Analysis (TGA) was used to follow the thermal transformations such as reagents decomposition, phase transformation, chemical stability, and volatilization of organic material of samples. The reagents and synthesized products by the different methods of synthesis were characterized using powder X-ray diffraction (XRD). All samples crystallize Er2Ru2O6 PDF (72-7620) in the cubic unit cell with Fd$\bar{3}$m (No. 227) space group and form a solid solution up to x = 0.15. Scanning electron microscopy (SEM) shows considerable variations and similitudes in sizes, very few phases and shapes of polycrystals can be observed. Polycrystalline samples prepared by solid-state reaction (SR) present a grain size varies between 77 nm to 250 nm.

Li2SrSiO4:Eu2+ phosphor prepared by the Pechini method and its application in white light emitting diode

2008 ◽  
Vol 23 (12) ◽  
pp. 3288-3294 ◽  
Author(s):  
Hong He ◽  
Renli Fu ◽  
Hai Wang ◽  
Xiufeng Song ◽  
Zhengwei Pan ◽  
...  
Keyword(s):  
Solid State ◽  
White Light ◽  
Solid State Reaction ◽  
Light Emitting Diode ◽  
Pechini Method ◽  
Sol Gel ◽  
Color Temperature ◽  
Light Emitting ◽  
White Leds ◽  
Luminescence Efficiency

Eu2+-doped Li2SrSiO4 phosphors were prepared by two different synthesis processes, the Pechini sol-gel route and solid-state reaction (SSR) method. Their morphology, crystal structure, and luminescence properties have been characterized. Li2SrSiO4:Eu2+ phosphors show broad and intensive excitation in the range of 390–480 nm and emit yellow-orange light extending from 500 to 700 nm. The luminescence efficiency of Li2SrSiO4: Eu2+ phosphors synthesized through the Pechini route is much better than that of phosphors prepared by solid-state reaction method. The application of phosphors from the Pechini route in white light emitting diodes (LEDs) has been investigated. The Commission Internationale de L’Eclairage (CIE) chromaticity coordinates and the correlated color temperature of these white LEDs have been calculated; they are comparable to corresponding values of commercial Y3Al5O12:Ce3+ converted white LEDs.

Electrical assessment of brownmillerite-type calcium ferrite materials obtained by proteic sol-gel route and by solid-state reaction using mollusk shells

2021 ◽  
pp. 122172
Author(s):  
Chrystian G.M. Lima ◽  
Allan J.M. Araújo ◽  
Rinaldo M. Silva ◽  
Rafael A. Raimundo ◽  
João P.F. Grilo ◽  
...  
Keyword(s):  
Solid State ◽  
Solid State Reaction ◽  
Sol Gel ◽  
Calcium Ferrite ◽  
Mollusk Shells

scholarly journals Sol-Gel Synthesis of the Double Perovskite Sr2FeMoO6 by Microwave Technique

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3876
Author(s):  
Jesús Valdés ◽  
Daniel Reséndiz ◽  
Ángeles Cuán ◽  
Rufino Nava ◽  
Bertha Aguilar ◽  
...  
Keyword(s):  
Particle Size ◽  
Hydrothermal Synthesis ◽  
Microwave Radiation ◽  
Structural Characteristics ◽  
Sol Gel ◽  
Synthesis Method ◽  
Double Perovskite ◽  
Synthesis Methods ◽  
X Ray ◽  
Sol Gel Synthesis

The effect of microwave radiation on the hydrothermal synthesis of the double perovskite Sr2FeMoO6 has been studied based on a comparison of the particle size and structural characteristics of products from both methods. A temperature, pressure, and pH condition screening was performed, and the most representative results of these are herein presented and discussed. Radiation of microwaves in the hydrothermal synthesis method led to a decrease in crystallite size, which is an effect from the reaction temperature. The particle size ranged from 378 to 318 nm when pH was 4.5 and pressure was kept under 40 bars. According to X-ray diffraction (XRD) results coupled with the size-strain plot method, the product obtained by both synthesis methods (with and without microwave radiation) have similar crystal purity. The Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) techniques showed that the morphology and the distribution of metal ions are uniform. The Curie temperature obtained by thermogravimetric analysis indicates that, in the presence of microwaves, the value was higher with respect to traditional synthesis from 335 K to 342.5 K. Consequently, microwave radiation enhances the diffusion and nucleation process of ionic precursors during the synthesis, which promotes a uniform heating in the reaction mixture leading to a reduction in the particle size, but keeping good crystallinity of the double perovskite. Precursor phases and the final purity of the Sr2FeMoO6 powder can be controlled via hydrothermal microwave heating on the first stages of the Sol-Gel method.

Annealing Effects on the Physical and Magnetic Properties of Tb1.5Y1.5Fe5O12 Films Nanoparticles Prepared by Sol-Gel Method

2013 ◽  
Vol 756 ◽  
pp. 91-98 ◽  
Author(s):  
Ftema W. Aldbea ◽  
Noor Bahyah Ibrahim ◽  
Mustafa Hj. Abdullah
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Annealing Temperature ◽  
Quartz Substrate ◽  
Sol Gel ◽  
Lattice Parameter ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Iron Garnet

Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900 °C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900°C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-raySpectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealingtemperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. Normal 0 21 false false false MS X-NONE X-NONE MicrosoftInternetExplorer4 Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900°C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900 °C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-ray Spectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealing temperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}

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