Effect of Epoxide Group in Thermoplastic Elastomer on the Properties of Polyamide6 and Low-Density Polyethylene Blends

2014 ◽  
Vol 979 ◽  
pp. 143-146 ◽  
Author(s):  
Surakit Tuampoemsab ◽  
Saad Riyajan ◽  
Thritima Sritapunya ◽  
Pornsri Pakeyangkoon

Studies on the effect of percentages of epoxide group in thermoplastic elastomer as a compatibilizer on properties of polyamide6 (PA6) and low-density polyethylene (LDPE) blends was successfully carried out in this study. Thermoplastic epoxidized natural rubber (TPENR), made from epoxidized natural rubber (ENR) and LDPE, prepared from 3 types of ENR, i.e., ENR-20, ENR-50 and ENR-70, with the ratio of 90/10 of LDPE/ENR by weight. TPENR was applied as a compatibilizer into the blend of PA6/LDPE/TPENR at the ratio by weight of 80/20/1 by using a twin screw extruder at 235°C. All test specimens were characterized for phase morphology, impact strength and rheological behaviour. Results exhibited that phase morphology of PA6/LDPE blend was incompatible. The addition of TPENR improved the compatibility of PA6/LDPE blends. With inclusion of TPENR-20 as a compatibilizer, the uniformity and the maximum reduction of dispersed phase sized were observed. Moreover, it was revealed that the rheological properties such as shear viscosity increased when compared with PA6/LDPE incompatible blend. In addition, it was found that the highest shear viscosity and also the highest impact strength were obtained for the blend of PA6/LDPE compatibilized by TPENR-20. This result was further supported by SEM images, which showed that the smallest dispersed phase size occurred when a TPENR-20 was used as a compatibilizer. So, it was clearly demonstrated in this study that the suitable type of TPENR, i.e., TPENR-20, has an effect on improving phase morphology and properties of PA6/LDPE blends.

2013 ◽  
Vol 33 (7) ◽  
pp. 579-588 ◽  
Author(s):  
S.T. Sam ◽  
H. Ismail ◽  
H.P.S. Abdul Khalil

Abstract In the present study, linear low density polyethylene (LLDPE)/soya powder blends were compatibilized with epoxidized natural rubber (ENR 50) and exposed to natural weathering. The exposure period for the blends was 1 year. It was found that the degradability of the compatibilized blends was higher than that of uncompatibilized blends. Fourier transform infrared (FTIR) spectra, the tensile test, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) were applied to analyze the degradability of the blends. IR spectra showed that the carbonyl index (CI) of the blends increased as a function of exposure period and soya powder content. The compatibilized blends gave higher carbonyl indices. The retention tensile strength and elongation at break (Eb) of the compatibilized blends after weathering was generally lower than for the uncompatibilized blends. The increase of crystallinity also indicated a reduction of the amorphous portion after degradation. The higher crystallinity in compatibilized blends further confirms the higher degradability of ENR 50 compatibilized blends. The weight loss and molecular weight change indicated that the incorporation of ENR 50 into LLDPE/soya powder blends can enhance the degradability of the blends upon outdoor exposure.


2014 ◽  
Vol 803 ◽  
pp. 310-316 ◽  
Author(s):  
S.T. Sam ◽  
Nurul Hani ◽  
H. Ismail ◽  
Nik Noriman ◽  
S. Ragunathan

Natural fiber reinforced composites are increasingly being used in various applications area. Therefore, the processing method and physical properties of these composites are very important parameters in product quality and quaranty. This paper focused on the tensile properties, Fourier transform infrared (FTIR) and water absorption of cogon grass (CG) with low density polyethylene (LDPE)/soya spent flour (SSF) composites. The tensile strength and elongation at break (Eb) of uncompatibilized CG with LDPE/ SSF decreased significantly with increasing of fiber content. However, the Young’s modulus increased with increasing of CG loading. The presence of epoxidized natural rubber (ENR 50) as a compatibilizer increased the tensile strength, Eband Young’s modulus of the composites when compared to uncompatibilized composites. Fourier transform infrared results show distinguishable peaks for compatibilized and uncompatibilized composites. The water absorption for both uncompatibilized and compatibilized composites increased from day 1 until day 21. The presence of ENR 50 as compatibilizer showed lower water absorption percentage compared to uncompatibilized composites.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1821
Author(s):  
Ildar I. Salakhov ◽  
Nadim M. Shaidullin ◽  
Anatoly E. Chalykh ◽  
Mikhail A. Matsko ◽  
Alexey V. Shapagin ◽  
...  

Low-temperature properties of high-density polyethylene (HDPE), low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), and their blends were studied. The analyzed low-temperature mechanical properties involve the deformation resistance and impact strength characteristics. HDPE is a bimodal ethylene/1-hexene copolymer; LDPE is a branched ethylene homopolymer containing short-chain branches of different length; LLDPE is a binary ethylene/1-butene copolymer and an ethylene/1-butene/1-hexene terpolymer. The samples of copolymers and their blends were studied by gel permeation chromatography (GPC), differential scanning calorimetry (DSC), 13С NMR spectroscopy, and dynamic mechanical analysis (DMA) using testing machines equipped with a cryochamber. It is proposed that such parameters as “relative elongation at break at −45 °C” and “Izod impact strength at −40 °C” are used instead of the ductile-to-brittle transition temperature to assess frost resistance properties because these parameters are more sensitive to deformation and impact at subzero temperatures for HDPE. LLDPE is shown to exhibit higher relative elongation at break at −45 °C and Izod impact strength at −20 ÷ 60 °C compared to those of LDPE. LLDPE terpolymer added to HDPE (at a content ≥ 25 wt.%) simultaneously increases flow properties and improves tensile properties of the blend at −45 °C. Changes in low-temperature properties as a function of molecular weight, MWD, crystallinity, and branch content were determined for HDPE, LLDPE, and their blends. The DMA data prove the resulting dependences. The reported findings allow one to understand and predict mechanical properties in the HDPE–LLDPE systems at subzero temperatures.


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