scholarly journals Enantiomeric Polylactide Blends in the Presence of Montmorillonite Clay

2018 ◽  
Vol 34 (6) ◽  
pp. 2716-2720
Author(s):  
Onanong Cheerarot ◽  
Yodthong Baimark

The stereocomplex polylactides (scPLAs) of the asymmetric poly(L-lactide)(PLLA)/poly(D-lactide) (PDLA) ratios from 80:20 to 60:40 were prepared via the simple melt blending method using an internal mixer at 200°C. An organo-modified clay, Cloisite® 30B, was used for nanocomposite preparation. The formation of the stereocomplex and nanocomposite structures were confirmed by differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD) and transmission electron microscopy (TEM). An increase in the PDLA content could enhance the stereocomplex formation. The presence of Cloisite®30B decreased the melting temperature and crystallinity of the blends. This was due to the thinner crystalline size generated and/or more disordered crystals.

e-Polymers ◽  
2017 ◽  
Vol 17 (5) ◽  
pp. 409-416 ◽  
Author(s):  
Yottha Srithep ◽  
Dutchanee Pholharn

AbstractPoly(l-lactide) (PLLA)/poly(d-lactide) (50/50) with plasticizer contents ranging from 2% to 16% w/w were prepared by melt blending using an internal mixer. Wide-angle X-ray diffraction, Fourier transform infrared spectroscopy and differential scanning calorimetry results confirmed that complete stereocomplex polylactide crystallites without any homocrystallites were produced. Compared to neat PLLA, the melting temperature of the stereocomplex polylactide and its plasticized samples was approximately 55°C higher. Higher plasticizer contents decreased glass transition temperature of the stereocomplex, which implied higher flexibility and enhanced the crystallization rate. However, the plasticizer in the stereocomplex reduced the thermal stability.


2013 ◽  
Vol 664 ◽  
pp. 538-542 ◽  
Author(s):  
Onusa Saravari ◽  
Phanitnan Srisuwan ◽  
Noppadon Kerddonfag ◽  
Wannee Chinsirikul

In this article, the effect of montmorillonite (MMT) concentration on the nucleation of polypropylene (PP) was investigated. The PP/MMT nanocomposites containing various content of MMT (0.075-3.0 wt%) were prepared by a melt blending process using an internal mixer, followed by compression molding into sheets. The nucleation effect of MMT was characterized by X-ray diffraction (XRD), wide angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC) techniques. XRD results indicated that the PP nanocomposites loaded with less than 1.5 wt% of MMT formed an exfoliated structure. DSC results showed that the crystallization temperature (Tc) of PP/MMT nanocomposites were higher than that of neat PP. Tc also increased with increasing MMT content, indicating that MMT was effective in nucleating PP crystal. WAXD patterns revealed that the addition of MMT did not affect the crystal structure of PP. Mechanical property tests showed that the tensile and impact strengths of the PP/MMT nanocomposites were better than those of neat PP when the MMT content was lower than 1.5 wt%.


2011 ◽  
Vol 364 ◽  
pp. 317-321 ◽  
Author(s):  
Siti Zulaiha Hairaldin ◽  
Wan Md Zin Wan Yunus ◽  
Nor Azowa Ibrahim

In this study, Octadecylamine Modified montmorillonites (ODAMMT) were used to prepare polylactide/polycaprolactone (PLA/PCL) clay nanocomposites. PLA and PCL were blend using an internal mixer by melt blending method. The other sample was blend with natrium monmorillonite (NaMMT) and Octadecylamine modified monmorillonite to produce PLA/PCL-NaMMT and PLA/PCL-ODAMMT. To characterize the polymer nanocomposite, X-ray diffraction (XRD), FTIR and SEM analysis were conducted. Comparison of morphology were made up between neat PLA/PCL, PLA/PCL with presence of of montmorillonite and octadecylamine modified monmorillonite respectively based on SEM micrograph. The number-average diameter was calculated for PLA/PCL, PLA/PCL-NaMMT, and PLA/PCL-ODAMMT.


2014 ◽  
Vol 1033-1034 ◽  
pp. 869-872
Author(s):  
Kun Yan Wang

Polypropylene (PP)/ethylene-vinyl acetate (EVA) blends were prepared using a twin-screw extruder by melt blending method. The influences of the EVA contents in PP/EVA blends on crystallization behavior and mechanical properties were investigated by X-ray diffraction (XRD) and differential scanning calorimetry (DSC). XRD results show that the EVA not change the crystal structure in the blends but only decrease the intensity of the diffraction peak. DSC results showed that the melting point and crystallization point decreased when EVA added to the blend. The tensile properties of PP/EVA blend become much better.


2017 ◽  
Vol 37 (8) ◽  
pp. 747-755 ◽  
Author(s):  
Zhiyuan Shen ◽  
Faliang Luo ◽  
Jianghua Du ◽  
Xiaomei Lei ◽  
Lijie Ji

Abstract The blends of poly (butylene terephthalate) (PBT) and 4,4′-dihydroxyphenyl (DHP) were prepared by melt blending, and the effects of DHP on the crystallization and melting behaviors of PBT were investigated by differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), and polarized optical microscopy (POM). The results showed that crystallization temperature and crystallinity of PBT apparently decreased with the addition of DHP. A remarkably decline in crystallization rate of PBT was achieved, and the blends had higher σe and q values than that of pure PBT as analyzed based on the Avrami equation and Lauritzen-Hoffman equation. The crystal structure of PBT did not change by the addition of DHP, while the spherulite size of PBT decreased.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Krisztian Nemeth ◽  
Nikolett Varro ◽  
Balazs Reti ◽  
Peter Berki ◽  
Balazs Adam ◽  
...  

Abstract In the present publication, multiwalled carbon nanotubes (MWCNT) coated with SiO2–MgO nanoparticles were successfully fabricated via sol–gel method to facilitate their incorporation into polymer matrices. Magnesium acetate tetrahydrate and tetraethyl orthosilicate were used as precursors. The coated MWCNTs were characterized by transmission electron microscopy (TEM), X–ray diffraction (XRD) and Raman spectroscopy methods. These investigation techniques verified the presence of the inorganic nanoparticles on the surface of MWCNTs. Surface coated MWCNTs were incorporated into polyamide (PA), polyethylene (PE) and polypropylene (PP) matrices via melt blending. Tensile test and differential scanning calorimetry (DSC) investigations were performed on SiO2–MgO/MWCNT polymer composites to study the reinforcement effect on the mechanical and thermal properties of the products. The obtained results indicate that depending on the type of polymer, the nanoparticles differently influenced the Young’s modulus of polymers. Generally, the results demonstrated that polymers treated with SiO2-MgO/MWCNT nanoparticles have higher modulus than neat polymers. DSC results showed that nanoparticles do not change the melting and crystallization behavior of PP significantly. According to the obtained results, coated MWCNTs are promising fillers to enhance mechanical properties of polymers.


Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Xianjie Yuan ◽  
Xuanhui Qu ◽  
Haiqing Yin ◽  
Zaiqiang Feng ◽  
Mingqi Tang ◽  
...  

This present work investigates the effects of sintering temperature on densification, mechanical properties and microstructure of Al-based alloy pressed by high-velocity compaction. The green samples were heated under the flow of high pure (99.99 wt%) N2. The heating rate was 4 °C/min before 315 °C. For reducing the residual stress, the samples were isothermally held for one h. Then, the specimens were respectively heated at the rate of 10 °C/min to the temperature between 540 °C and 700 °C, held for one h, and then furnace-cooled to the room temperature. Results indicate that when the sintered temperature was 640 °C, both the sintered density and mechanical properties was optimum. Differential Scanning Calorimetry, X-ray diffraction of sintered samples, Scanning Electron Microscopy, Energy Dispersive Spectroscopy, and Transmission Electron Microscope were used to analyse the microstructure and phases.


Clay Minerals ◽  
2009 ◽  
Vol 44 (1) ◽  
pp. 35-50 ◽  
Author(s):  
Yun Huang ◽  
Xiaoyan Ma ◽  
Guozheng Liang ◽  
Hongxia Yan

AbstractMelt blending using a twin-screw extruder was used to prepare composites of polypropylene (PP)/organic rectorite (PR). The organic rectorite (OREC) was modified with dodecyl benzyl dimethyl ammonium bromide (1227). Wide-angle X-ray diffraction (WAXD) and transmission electron microscopy were used to investigate the dispersion of OREC in the composites. The d spacings of OREC in PR composites was greater than in OREC itself. The dispersion of OREC particles in the PP polymer matrix was fine and uniform when the clay content was small (2 wt.%). The rheology was characterized using a capillary rheometer. The processing behaviour of the PR system improved as the amount of OREC added increased. Non-isothermal crystallization kinetics were analysed using differential scanning calorimetry. It was shown that the addition of OREC had a heterogeneous nucleation effect on PP, and can accelerate the crystallization. However, only when fine dispersion was achieved, and at lower rates of temperature decrease, was the crystallinity greater. Wide-angle X-ray diffraction and polarized light microscopy were used to observe the crystalline form and crystallite size. The PP in the PR composites exhibited an a-monoclinic crystal form, as in pure PP, and in both cases a spherulite structure was observed. However, the smaller spherulite size in the PR systems indicated that addition of OREC can reduce the crystal size significantly, which might improve the ‘toughness’ of the PP. The mechanical properties (tensile and impact strength) improved when the amount of OREC added was appropriate. Dynamic mechanical analysis showed that the storage modulus (E′) and loss modulus (E″) of the nanocomposites were somewhat greater than those of pure PP when an appropriate amount of OREC was added. Finally, thermogravimetric analysis showed that the PR systems exhibited a greater thermal stability than was seen with pure PP.


2013 ◽  
Vol 785-786 ◽  
pp. 123-126
Author(s):  
Ying Ye ◽  
Kun Yan Wang ◽  
Ge Chang ◽  
Qian Ying Jiang

Polypropylene/organoclay modified by dodecanol phase change material were prepared by melt blending method. The thermal stability and crystallization behavior was studied by thermogravimetry (TG), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). TG results indicated the window of processing of PP could be improved by adding small amount organoclay modified by dodecanol to the blend. DSC showed the organoclay modified by dodecanol affected the crystallization behavior of PP as heterogeneous nucleation agent. XRD results show that the organoclay modified by dodecanol does not change the crystal structure in the blends but only decrease the intensity of the diffraction peak.


1991 ◽  
Vol 246 ◽  
Author(s):  
J.A. Horton ◽  
E.P. George ◽  
C.J. Sparks ◽  
M.Y. Kao ◽  
O.B. Cavin ◽  
...  

AbstractA survey by differential scanning calorimetry (DSC) and recovery during heating of indentations on a series of nickel-aluminum alloys showed that the Ni-36 at.% Al composition has the best potential for a recoverable shape memory effect at temperatures above 100°C. The phase transformations were studied by high temperature transmission electron microscopy (TEM) and by high temperature x-ray diffraction (HTXRD). Quenching from 1200°C resulted in a single phase, fully martensitic structure. The initial quenched-in martensites were found by both TEM and X-ray diffraction to consist of primarily a body centered tetragonal (bct) phase with some body centered orthorhombic (bco) phase present. On the first heating cycle, DSC showed an endothermic peak at 121°C and an exothermic peak at 289°C, and upon cooling a martensite exothermic peak at 115° C. Upon subsequent cycles the 289°C peak disappeared. High temperature X-ray diffraction, with a heating rate of 2°C/min, showed the expected transformation of bct phase to B2 between 100 and 200°C, however the bco phase remained intact. At 400 to 450°C the B2 phase transformed to Ni2Al and Ni5Al3. During TEM heating experiments a dislocation-free martensite transformed reversibly to B2 at temperatures less than 150°C. At higher temperatures (nearly 600°C) 1/3, 1/3, 1/3 reflections from an ω-like phase formed. Upon cooling, the 1/3, 1/3, 1/3 reflections disappeared and a more complicated martensite resulted. Boron additions suppressed intergranular fracture and, as expected, resulted in no ductility improvements. Boron additions and/or hot extrusion encouraged the formation of a superordered bct structure with 1/2, 1/2, 0 reflections.


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