scholarly journals Characterization of the Interface Between the Bulk Glass Forming Alloy Zr41Ti14Cu12Ni10Be23 with Pure Metals and Ceramics

2000 ◽  
Vol 15 (7) ◽  
pp. 1617-1621 ◽  
Author(s):  
Jan Schroers ◽  
Konrad Samwer ◽  
Frigyes Szuecs ◽  
William L. Johnson

The reaction of the bulk glass forming alloy Zr41Ti14Cu12Ni10Be23 (Vit 1) with W, Ta, Mo, AlN, Al2O3, Si, graphite, and amorphous carbon was investigated. Vit 1 samples were melted and subsequently solidified after different processing times on discs of the different materials. Sessile drop examinations of the macroscopic wetting of Vit 1 on the discs as a function of temperature were carried out in situ with a digital optical camera. The reactions at the interfaces between the Vit 1 sample and the different disc materials were investigated with an electron microprobe. The structure and thermal stability of the processed Vit 1 samples were examined by x-ray diffraction and differential scanning calorimetry. The results are discussed in terms of possible applications for composite materials.

2011 ◽  
Vol 691 ◽  
pp. 23-26 ◽  
Author(s):  
C. Triveño Rios ◽  
Conrado R. M. Afonso ◽  
Claudemiro Bolfarini ◽  
Walter José Botta Filho ◽  
Claudio Shyinti Kiminami

Bulk glassy alloys based on the Fe-Co-B-Si-Nb system have already achieved high levels of mechanical strength. The present work investigated the microstructural evolution of Fe43.2Co28.8B19.2Si4.8Nb4 alloy during the spray forming and wedge mold casting processes, with emphasis on the formation of amorphous phase. The microstructure was evaluated by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). The region outer the spray deposit showed the formation of an amorphous structure with a thickness of ~2.5 mm, while that of the wedge-shaped sample exhibited a thickness of up to ~1.5 mm, suggesting that both processes show a promising potential for the production of bulk glass alloys.


2012 ◽  
Vol 490-495 ◽  
pp. 3868-3873 ◽  
Author(s):  
Xiao Hong Yang ◽  
Xi Peng Nie ◽  
Jian Zhong Jiang

Bulk metallic glasses (BMGs) of Cu45Zr48-xAl7Tix with x= 0, 1.5, and 3 at.% were prepared by copper mould casting. The corrosion resistance of the BMGs with different Ti contents was examined by potentiodynamic polarization tests and weight loss measurements in 1 N NaOH, 1 N H2SO4, 1 N H2SO4 + 0.01 N NaCl and 0.5 N NaCl solutions, respectively. The newly-developed BMGs’ corrosion resistance in Cl-- or both H+ and Cl--ions containing solutions can be greatly enhanced. The influence of Ti addition on glass forming ability (GFA) and thermal stability was investigated by x-ray diffraction and differential scanning calorimetry in detail. The alloy containing 1.5 at.% Ti exhibits the largest GFA, the critical size comes up to 10 mm in diameter.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Jianjun Chen ◽  
Yueyue Jia ◽  
Zhiye Zhang ◽  
Xinlong Wang ◽  
Lin Yang

We investigated the changes in the conformation and crystalline structure of polypropylene (PP) using a combination of Fourier transform infrared spectroscopy (FTIR), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC) based on PP/chlorinated PP (CPP)/polyaniline (PANI) composites. The DSC heating thermograms and WAXD patterns of the PP/CPP/PANI composites showed that theβ-crystal was affected greatly by the CPP content. Characterization of the specific regularity in the infrared band variation showed that the conformational orders of the helical sequences in PP exhibited major changes that depended on the CPP content. Initially, the intensity ratio ofA840/A810increased with the CPP concentration and reached its maximum level when the CPP content was <13.22% before decreasing as the CPP content increased further. The effect of increased temperature on the conformation of PP was studied by in situ FTIR. Initially, the intensity ratio ofA999/A973decreased slowly with increasing the temperature up to 105°C before decreasing sharply with further increases in temperature and then decreasing slowly again when the temperature was higher than 128°C.


2016 ◽  
Vol 71 (12) ◽  
pp. 1199-1209
Author(s):  
Vera A. Hartdegen ◽  
Maximilian S. Hofmayer ◽  
Konstantin Karaghiosoff ◽  
Thomas M. Klapötke

AbstractOn the basis of 1,2-bis(5-tetrazolo)ethane (BTE) the corresponding twofold vinyl and allyl N-substituted derivatives were synthesized using 1,2-dibromoethane and allyl bromide, respectively. The compounds were obtained as two different constitutional isomers. Both species were analyzed using NMR and IR spectroscopy, elemental analysis, as well as mass spectrometry. In the case of the diallyl bistetrazoles, the two isomers were characterized using 2D NMR spectroscopy. The synthesis of the divinyl compounds gave crystals of the 2,2′-N-substituted isomer, which were analyzed by single-crystal X-ray diffraction. The thermal stability of the compounds was determined using differential scanning calorimetry (DSC) and gave decomposition temperatures around 190°C and 230°C. For the investigation of the inherent energetic potential, sensitivities toward physical stimuli and detonation parameters were determined. The compounds turned out to be insensitive toward friction and impact and possess moderate energetic properties.


2014 ◽  
Vol 904 ◽  
pp. 7-9
Author(s):  
Xiao Hua Gu ◽  
Xi Wei Zhang ◽  
Bao Yun Xu ◽  
Peng Zeng

In this paper, the diphenyl methane diisocyanate (MDI) was used to modify montmorillonoid (MMT) and got the organic montmorillonite (OMMT), which was used with the monomers of PET by in situ polymerization method to prepare PET/MMT nanocomposition. The OMMT was analyzed by the X ray diffraction (XRD) to test the change of the spacing layer. Dispersion of MMT in the PET/MMT nanocomposites were studied with XRD and SEM and by means of thermogravimetric analyzer (TGA) on the thermal stability of PET/MMT nanocomposites. The results showed that, MDI modified MMT successfully, and the compatibility of MMT and PET was increased .


2012 ◽  
Vol 182-183 ◽  
pp. 249-253
Author(s):  
Jun Qiao ◽  
Jia Wei Shen ◽  
Xiang Hong Huang ◽  
Qian Feng Zhang

PMMA/MMT nanocomposites has been prepared by using methyl methacrylate (MMA), montmorillonite (MMT) and ethanolamine as the raw materials via an in-situ free radical polymerization process. The as-prepared nanocomposites were characterized by Fourier transformation infrared spectroscopy (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The results show that the poly(methyl methacrylate) and inorganic montmorillonite have been effectively combined. The structure and thermal stability of the as-prepared nanocomposites are different from the content of MMT in the nanacomposites.


2014 ◽  
Vol 915-916 ◽  
pp. 780-783
Author(s):  
Hong Wang ◽  
Ming Tian Li ◽  
Yue Lu ◽  
Di Liu

Pyrrole and m-toluidine copolymer (P(PY/MT)) / montmorillonite (MMT) Composites were prepared by in situ chemical polymerization of pyrrole with m-toluidine monomer in the presence of montmorillonite. The structural, morphological and thermal properties of these composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). X-ray diffraction result for P(PY/MT)-MMT illuminated the intercalation of P(PY/MT) copolymer between the clay layers. The FT-IR result showed the successful incorporation of montmorillonite clay in the prepared P(PY/MT)/MMT composite. The higher thermal stability of high MMT content rate might be attributed to its higher chain compactness due to the interfacial interaction between the P(PY/MT) and the clay.


2009 ◽  
Vol 151 ◽  
pp. 145-149 ◽  
Author(s):  
Viorica Gaina ◽  
Constantin Gaina ◽  
Mihaela Olaru

A novel silver/polysulfone nanocomposite membrane was prepared by a convenient ultraviolet irradiation technique, through in situ reduction of silver salt (AgNO3) added to a solution of commercial UDEL polyethersulfone dissolved in N-methyl-2-pyrrolidinone (NMP). The UV-reduction of Ag+ to Ag0 nanoparticles was confirmed by means of UV-vis spectroscopy, from aggregation phenomena. The effects of dispersion of silver nanoparticles within polysulfone matrix were investigated by means of ATR-FTIR, dynamic mechanical thermal analysis and differential scanning calorimetry. Using X-ray diffraction, it was shown that annealing produced silver crystallites of 70-90 nm across, which are partially textured in “sheetlike” {110} planes.


e-Polymers ◽  
2013 ◽  
Vol 13 (1) ◽  
Author(s):  
Matko Erceg ◽  
Dražan Jozić

Abstract Poly(3-hydroxybutyrate)/Cloisite25A (PHB/25A) nanocomposites were prepared by solution-intercalation method. The intercalation of PHB chains between the layers of Cloisite25A was observed by X-ray diffraction (XRD). Differential scanning calorimetry (DSC) and non-isothermal thermogravimetry (TG) analysis were performed to study the thermal properties, crystallization and the thermal degradation of the prepared nanocomposites. DSC analysis indicates that Cloisite25A acts as a nucleating agent and increases the crystallization rate of PHB, but due to intercalation reduces its overall degree of crystallinity. TG analysis shows that addition of Cloisite25A enhances the thermal stability of PHB.


2014 ◽  
Vol 941-944 ◽  
pp. 334-337
Author(s):  
Hong Wang ◽  
Rui Song Yang ◽  
Ying Wang

Poly (m-toluidine)(PMT) / montmorillonite (MMT) Composites with thermal stability were synthesized by in situ chemical polymerization of m-toluidine monomer in the presence of montmorillonite. The PMT /MMT composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). The FT-IR result displayed the successful incorporation of montmorillonite clay in the prepared PMT/MMT composite. X-ray diffraction result for PMT/MMT showed the intercalation of PMT between the clay layers. The higher thermal stability of high MMT content rate might be attributed to its higher chain compactness due to the interfacial interaction between the PMT and the .MMT.


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