Crystallization and melting behavior of i-PP: a perspective from Flory's thermodynamic equilibrium theory and DSC experiment

PA6/polypropylene (PP) blends are investigated for obtaining balanced strength and toughness. The focus of this study is to understand the effect of PP content on mechanical property, water absorption, impact strength, thermal behavior, and morphology of PP in the absence and presence of PP‐g‐maleic anhydride compatibilizer. In comparison to pure PA6, all blends have higher impact strength with 161 and 124% increase at 5 wt % PP content in uncompatibilized and compatibilized blends (UB and CB), respectively. Morphology of impact fractured samples shows brittle fracture in the case of CB. scanning electron microscope of cryogenically fractured samples show decrease in domain size and change in shape from ellipsoid to spherical, from UB to CB. Then, 75% reduction in water absorption is observed for 50 wt % PP content UB. Postwater absorption yield strength (YS) remains constant above 10 wt % PP in both UB and CB and decrease in YS is less at higher PP content in CB. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47690.

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 2 more Smart Citations

Influence of PP content on mechanical properties, water absorption, and morphology in PA6/PP blend

Aparna

Purnima

2019

“…[66][67][68][69] The standard values for heat of melting-PA11 = 244 J/g 70,71 , PHB = 146 J/g, 72 and PP = 207 J/g. 73 Supporting Information Table S3 shows the % crystallinity for PA11, PP, PP-g-MA, and PHB, while crystallinity of the formed blends was shown in Table V. Due to phase separation and differential crystallization of PP and PA 11, the noncompatible binary blend has very low values of % crystallinity.…”

Section: Thermal Analysismentioning

confidence: 99%

Novel approach for the preparation of a compatibilized blend of nylon 11 and polypropylene with polyhydroxybutyrate: Mechanical, thermal, and barrier properties

Gadgeel

Mhaske

2019

This article comprises of the interaction in the immiscible polymer system of nylon 11 (PA 11), polypropylene (PP), and polyhydroxybutyrate (PHB). Reactive compatibilization extrusion method with maleic anhydride-grafted polypropylene (PP-g-MA) is used to achieve compatibility within the polymer. To further improve the interaction of the blend at interphase, PHB was added as a dispersive phase in a concentration varying from 10 to 40% of the total batch. Addition of PHB motives the excellent dispersion of PP chain in PA 11 and assures the compatibility between the phases of PA 11 and PP-g-MA. The entire system of tertiary and binary phases was blended in a twin-screw extruder at different composition. The macro-optimal tensile strength, Young's modulus, bending strength, and notched impact strength of PA11/PP systems were found to be superior as compared to their noncompatibilized systems. The degradation temperature of the blends of PA11/PP and PA11/PHB/PP with and without compatibilizer was evaluated by thermogravimetric analysis (TGA). It was found that the high temperature of degradation was required for compatibilized ternary blend than that of the compatibilized binary blend. The distortion temperature of the systems was studied with the help of heat deflection temperature (HDT) and found to be advanced for blend having a higher concentration of the dispersed phase. Differential scanning calorimetry (DSC) was used to determine the % crystallinity, melting, and crystallization temperature of this system. Chemical resistance and barrier properties of the different compatibilized and noncompatibilized blends were studied. PHB dispersed phase with a reactive compatibilizer cause enhancement in chemical resistance and barrier properties of the blend.

Effect of the elastomer viscosity on the morphology and impact behavior of injection molded foams based on blends of polypropylene and polyolefin elastomers

Muñoz-Pascual

Saiz‐Arroyo²,

Vananroye

et al. 2020

The impact resistance of injection‐molded polypropylene (PP) parts is severely reduced when they are foamed. It is necessary to implement strategies, such as elastomer toughening, to increase the impact behavior of foamed parts. However, the knowledge on the effect of elastomer addition on the morphology, cellular structure, and impact of injection‐molded cellular parts is very limited. In this work, foamed parts based on blends of PP and polyolefin elastomers have been produced and characterized. A high and a low viscosity octene‐ethylene copolymer (EOC) and a high viscosity butene‐ethylene copolymer (EBC) were employed. The blends have been thermally and rheological characterized. Solids materials and foams (relative density 0.76) were injection‐molded. The solid phase and cellular structure morphologies were studied using scanning electron microscopy. The results showed that elastomer toughening has been successful to obtain an improvement of the impact behavior in solid and cellular polymers. In this case, EOC materials provide an appropriate interfacial adhesion and optimized cellular structure which results in high impact resistance. The optimum elastomer to improve the properties is the EOC with a higher viscosity which provides impact resistance with n values below 3 due to the toughening of polymer matrix, thick skin thickness, and low cell size.