High Energy Ball Milling and Liquid Crystal Template Method: A Successful Combination for the Preparation of Magnetic Nano-Platforms

2021 ◽  
Vol 21 (5) ◽  
pp. 2930-2934
Author(s):  
Alessandra Scano ◽  
Edmond Magner ◽  
Martina Pilloni ◽  
Davide Peddis ◽  
Franca Sini ◽  
...  

In this study, we present the preparation of superparamagnetic ordered mesoporous silica (SOMS) for biomedical applications by the combination of high energy ball milling (HEBM) and the liquid crystal template method (LCT) to produce a material comprised of room temperature superparamagnetic Fe3O4 nanoparticles in a MCM-41 like mesostructured silica. In a typical synthesis, a mixture of Fe2O3 and silica was sealed in a stainless-steel vial with steel balls. Ball milling experiments were performed in a vibratory mill apparatus. The milling process produced nanocomposites with an average size ranging from ∼100–200 nm, where the Fe3O4 nanoparticles (4.8 nm size) are homogeneously dispersed into the amorphous SiO2 matrix. The obtained nanocomposite has been used for the preparation of the SOMS through the LCT method. Structural, morphological and textural characterization were performed using X-ray powder diffraction, transmission electron microscopy and nitrogen sorption analysis. Field dependence of magnetization was investigated and showed superparamagnetic behaviour at 300 K with a value of saturation magnetization (Ms) that is of interest for biomedical applications.

2014 ◽  
Vol 802 ◽  
pp. 29-34
Author(s):  
Leandro Koji Kayano ◽  
Daniel Murusawa ◽  
Gilda Maria Cortez Pereira ◽  
Alfeu Saraiva Ramos

This work presents the results on the high-energy ball milling and hot pressing of Ni-48Ti-2Sn and Ni-45Ti-5Sn (at-%) powder mixtures. The milling process was performed in a planetary ball mill using stainless steel vial (225 mL) and hardened steel balls (19 mm diameter), rotary speed of 300 rpm, and a ball-to-powder weight ratio of 10:1. Samples were collected into the vial after different milling times: 60, 180 and 300 min. In the sequence, wet milling (isopropyl alcohol) was adopted up to 720 min in order to increase the powder yield into the vials. The as-milled and hot-pressed samples were characterized by X-ray diffraction, electron scanning microscopy, and energy dispersive spectrometry. Results indicated that the ductile particles were promptly cold-welded during the initial milling times. XRD patterns of the Ni-48Ti-2Sn powder mixture indicated that the peaks of Ni, Ti and Sn disappeared after milling for 3h. Following, peaks of NiTi and Ni4Ti3were preferentially formed during milling of Ni-Ti-Sn powders. A large amount of fine powders was yielded into the vial after wet milling for 720 min only. No significant carbon or oxygen contamination was detected by EDS analysis. Hot pressing produced homogeneous and dense samples which presented microstructures containing a large amount of the NiTi compound.


2012 ◽  
Vol 727-728 ◽  
pp. 233-238
Author(s):  
Gilda Maria Cortez Pereira ◽  
Marisa Aparecida de Souza ◽  
Tomaz Manabu Hashimoto ◽  
Vinicius André Rodrigues Henriques ◽  
Alfeu Saraiva Ramos

This work discusses on the preparation of Ni-45Ti-5Mo, Ni-40Ti-10Mo and Ni-46Ti-2Mo-2Zr (at-%) alloys by high-energy ball milling and hot pressing, which are potentially attractive for dental and medical applications. The milling process was performed in stainless steel balls (19mm diameter) and vials (225 mL) using a rotary speed of 300rpm and a ball-to-powder weight ratio of 10:1. Hot pressing under vacuum was performed in a BN-coated graphite crucible at 900°C for 1 h using a load of 20 MPa. The milled and hot-pressed materials were characterized by X-ray diffraction, electron scanning microscopy, and electron dispersive spectrometry. Peaks of B2-NiTi and Ni4Ti3were identified in XRD patterns of Ni-45Ti-5Mo, Ni-40Ti-10Mo and Ni-46Ti-2Mo-2Zr powders milled for 1h. The NiTi compound dissolved small Mo amounts lower than 4 at%, which were measured by EDS analysis. Moreover, it was identified the existence of an unknown Mo-rich phase in microstructures of the hot-pressed Ni-Ti-Mo alloys.


2006 ◽  
Vol 54 (1) ◽  
pp. 93-97 ◽  
Author(s):  
J.L. Li ◽  
L.J. Wang ◽  
G.Z. Bai ◽  
W. Jiang

2001 ◽  
Vol 16 (6) ◽  
pp. 1636-1643 ◽  
Author(s):  
L. B. Kong ◽  
J. Ma ◽  
T. S. Zhang ◽  
W. Zhu ◽  
O. K. Tan

Partially reacted mixtures of Pb(ZrxTi1−x)O3 and its corresponding starting oxide components were obtained by a high-energy ball milling process. The partially reacted powders were characterized by x-ray diffraction and scanning electron microscopy techniques. The sintering behavior of the milled mixtures has demonstrated a distinct volumetric expansion before the densification of the samples, which clearly shows the occurrence of a reactive sintering process of the partially reacted powders. Such process requires a lower densification temperature as compared with the PZT powders produced by the conventional solid-state reaction process. PZT ceramics were found to form directly from the partially reacted powders sintered at 900–1200 °C. The dielectric and ferroelectric properties of the PZT ceramics as a function of sintering temperature and milling time were also studied and discussed.


2012 ◽  
Vol 86 ◽  
pp. 122-124 ◽  
Author(s):  
Sajjad Amirkhanlou ◽  
Mostafa Ketabchi ◽  
Nader Parvin

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