Preparation and Characterization of Polypropylene/Clay Nanocomposites

2011 ◽  
Vol 55-57 ◽  
pp. 1584-1587 ◽  
Author(s):  
Li Mei Wang

Polypropylene(PP)/clay nanocomposites were prepared by solution blending. The microstructure of PP/clay nanocomposites was studied by wide-angle X-ray diffraction (XRD) analysis. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were used to investigate thermal properties of PP/clay nanocomposites. XRD pattern prove that clay layers were exfoliated into nanometer size in PP matrix and that α-Phase crystallite was the main crystallite of PP in PP/clay nanocomposites. TGA examinations confirmed that the maximum decomposition temperature of PP/clay nanocomposites was higher than that of neat PP and that the thermal stability of PP/clay nanocomposites rose noticeably. Results of DSC scans showed the crystalliztion temperature of nanocomposites was slightly bigger than that of pure PP due to the efficient nucleating effects of clay layers.

2011 ◽  
Vol 55-57 ◽  
pp. 1588-1592
Author(s):  
Li Mei Wang

Clay was organically modified with one kind of ionic liquild. Organical clay obtained was used to prepare poly(propylene) (PP)/clay nanocomposites by solution blending. Flourier transform infrared (FTIR), wide-angle X-ray diffraction (XRD) and thermogravimetric analysis (TGA) revealed that the ionic liquild was loaded in the galleries of organically modified clay. TGA result show the thermal stability of organically modified clay was superior to clay. XRD patterns indicated that the d-spacing of clay layers increased to 2.96 nm from 1.22 nm of clay. XRD patterns of PP/clay nanocomposites show that clay layers were dispersed in PP matrix by nanometer size.


2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Limei Wang ◽  
Aihua He

Polypropylene (PP)/clay nanocomposites were synthesized by in situ intercalative polymerization with TiCl4/MgCl2/clay compound catalyst. Microstructure and thermal properties of PP/clay nanocomposites were studied in detail. Fourier transform infrared (FTIR) spectra indicated that PP/clay nanocomposites were successfully prepared. Both wide-angle X-ray diffraction (XRD) and transmission electron microscopy (TEM) examination proved that clay layers are homogeneously distributed in PP matrix. XRD patterns also showed that theαphase was the dominate crystal phase of PP in the nanocomposites. Thermogravimetric analysis (TGA) examinations confirmed that thermal stability of PP/clay nanocomposites was markedly superior to pure PP. Differential scanning calorimetry (DSC) scans showed that the melt temperature and the crystallinity of nanocomposites were slightly lower than those of pure PP due to crystals imperfections.


Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 3035
Author(s):  
Dovydas Karoblis ◽  
Diana Griesiute ◽  
Kestutis Mazeika ◽  
Dalis Baltrunas ◽  
Dmitry V. Karpinsky ◽  
...  

In this study, a highly crystalline bismuth ferrite (BFO) powder was synthesized using a novel, very simple, and cost-effective synthetic approach. It was demonstrated that the optimal annealing temperature for the preparation of highly-pure BFO is 650 °C. At lower or higher temperatures, the formation of neighboring crystal phases was observed. The thermal behavior of BFO precursor gel was investigated by thermogravimetric and differential scanning calorimetry (TG-DSC) measurements. X-ray diffraction (XRD) analysis and Mössbauer spectroscopy were employed for the investigation of structural properties. Scanning electron microscopy (SEM) was used to evaluate morphological features of the synthesized materials. The obtained powders were also characterized by magnetization measurements, which showed antiferromagnetic behavior of BFO powders.


2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jiangtao Xing ◽  
Weili Wang ◽  
Wenzheng Xu ◽  
Tianle Yao ◽  
Jun Dong ◽  
...  

In order to improve the safety of hexanitrohexaazaisowurtzitane (CL-20), submicron CL-20 particles were prepared by a siphon ultrasonic-assisted spray refining experimental device. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC), and the impact sensitivity of the samples was tested. The results show that the particle size of siphon-refined CL-20 is about 800 nm~1 μm, which is more smooth, mellow, and dense than that of CL-20 prepared by a traditional pressure-refined method. The peak diffraction angle of pressure- and siphon-refined CL-20 is basically the same as that of raw CL-20, and their crystal forms are ε type. The peak strength of pressure- and siphon-refined CL-20 decreased obviously. The apparent activation energy of pressure-refined CL-20 and siphon-refined CL-20 is 13.3 kJ/mol and 11.95 kJ/mol higher than that of raw CL-20, respectively. The thermal stability of CL-20 is improved. The activation enthalpy (ΔH#) is significantly higher than that of raw CL-20, and the characteristic drop is 70.4% and 82.7% higher than that of raw CL-20. The impact sensitivity of siphon-refined CL-20 is lower than that of pressure-refined CL-20, so the safety performance of an explosive is improved obviously.


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.


2018 ◽  
Vol 32 (8) ◽  
pp. 1078-1091 ◽  
Author(s):  
Sibel Erol Dağ ◽  
Pınar Acar Bozkurt ◽  
Fatma Eroğlu ◽  
Meltem Çelik

A series of polystyrene (PS)/unmodified Na-montmorillonite (Na-MMT) composites were prepared via in situ radical polymerization. The prepared composites were characterized using various techniques. The presence of various functional groups in the unmodified Na-MMT and PS/unmodified Na-MMT composite was confirmed by Fourier transform infrared spectroscopy. Morphology and particle size of prepared composites was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). According to the XRD and TEM results, the interlayer spacing of MMT layers was expanded. SEM images showed a spongy and porous-shaped morphology of composites. TEM revealed the Na-MMT intercalated in PS matrix. The thermal stability of PS/unmodified Na-MMT composites was significantly improved as compared to PS, which is confirmed using thermogravimetric analysis (TGA). The TGA curves indicated that the decomposition temperature of composites is higher at 24–51°C depending on the composition of the mixture than that of pure PS. The differential scanning calorimetry (DSC) results showed that the glass transition temperature of composites was higher as compared to PS. The moisture retention, water uptake, Brunauer–Emmett–Teller specific surface area, and specific pore volume of composites were also investigated. Water resistance of the composites can be greatly improved.


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.


2021 ◽  
Vol 2129 (1) ◽  
pp. 012092
Author(s):  
Suffi Irni Alias ◽  
Banjuraizah Johar ◽  
Syed Nuzul Fadzli Adam ◽  
Mustaffa Ali Azhar Taib ◽  
Fatin Fatini Othman ◽  
...  

Abstract The porcelain formulation containing percentages of treated FGD sludge waste from 5% up to 15% in replacement of feldspar were prepared. The porcelain mixture formulation were mixed by high energy planatery mill at speed 300 rpm for 1 hours. The powder were compacted by using hydraulic press and sintered at temperature 1200 °C for 3 hours. The sintered samples were characterized using X-ray fluorescene (XRF), X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) and Thermogravimetry/Differential scanning calorimetry (TGA/DCS). The primary effect concerning the addition of treated FGD sludge was the change of intensity composition (gypsum and anhydrate) in porcelain formulation. The XRD analysis has shown that the main component in sludge waste were gypsum and anhydrate.


2018 ◽  
Vol 26 (3(129)) ◽  
pp. 17-22 ◽  
Author(s):  
Xichao Sun ◽  
Yeqian Ge

In order to provide a theoretical basis for the preparation and spinnability of two-component materials, poly(3-hydroxybutyrate-co-3-hydroxyvalerate)(PHBV) and polypropylene grafting maleic anhydride (PP-g-MAH) blends were prepared by melt mixing with different ratios (100/0, 75/25, 50/50, 25/75, 0/100). Properties of the blends system were investigated by means of a mixed rheometer, scanning electron microscope, simultaneous thermal analyser, differential scanning calorimetry and X-ray diffraction. The results demonstrate that PHBV/PP-g-MAH blends exhibit different morphology of the sea-island with a change in the mix ratio. The initial thermal decomposition temperature of PHBV in the blending system is over 250 °C, which means the thermal stability of PHBV is markedly improved. The crystallisation of PHBV varied according to the blending process parameter. When the cooling velocity increases, the crystallisation peak becomes wide, the temperature of crystallisation decreases, and the crystallisation temperature of PHBV increases significantly. PHBV has a high sensitivity to variation in the shear rate, and PHBV/PP-g-MAH blends have the mixing characteristic of shear thinned liquid. There is no diffraction peak at 2θ = 22.8°, and this result certifies that PP-g-MAH changes the crystal form of PHBV. and that PP-g-MAH addition is beneficial to the spinnability of PHBV. Results show that the interplay between PHBV and PP-g-MAH is of great significance and universal for both plastics and fibres.


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.


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