Compatibilization Effects of PE-g-MA on Mechanical,Thermal and Swelling Properties of High Density Polyethylene/Natural Rubber/Thermoplastic Tapioca Starch Blends

Effect of polyethylene grafted maleic anhydride (PE-g-MA) on mechanical, thermal and swelling characteristic of high density polyethylene (HDPE)/natural rubber (NR)/thermoplastic tapioca starch (TPS) blends were studied. The measurements from differential scanning calorimetric (DSC), dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA), proved the effectiveness of PE-g-MA as compatibilizer in improving the miscibility between HDPE/NR – TPS blends. A decrement in crystallinity index was found after adding PE-g-MA. It is due to restriction in mobility of the HDPE chains. In the presence of PE-g-MA, the blends have better thermal stability. On top of that, the storage modulus which is reflected to the blend stiffness also increased as indicated the improvement in HDPE/NR – TPS interaction.     

Compatibilization of SBR/NBR blends using chemically modified styrene‐co‐butadiene rubber Part 2. Effect of compatibilizer loading

The present work focuses on the compatibization of styrene‐co‐butadiene rubber (SBR)/acrylonitrile‐co‐butadiene rubber (NBR) blends with dichlorocarbene modified styrene‐co‐butadiene rubber (DCSBR) as a function of concentration of compatibilizer and composition of the blend. FTIR studies, differential scanning calorimetry and dynamic mechanical analysis reveal molecular level miscibility in the blends in the presence of compatibilizer. The formation of interfacial bonding is assessed by analysis of swelling behaviour, cure characteristics, stress–strain data and mechanical properties. These studies show that the compatibilizing action of DCSBR becomes more prominent as the proportion of NBR in the blend increases. The resistance of the vulcanizate towards thermal and oil ageing improved with compatibilization. The change in technological properties is correlated with the crosslink density of the blends assessed from swelling and stress–strain data. © 2001 Society of Chemical Industry     

Tensile properties and morphology of the dynamically cured EPDM and PP/HDPE ternary blends

The tensile properties and morphology of the polyolefin ternary blends of ethylenepropylene–diene terpolymer (EPDM), polypropylene and high density polyethylene were studied. Blends were prepared in a laboratory internal mixer where EPDM was cured in the presence of PP and HDPE under shear with dicumyl peroxide (DCP). For comparison, blends were also prepared from EPDM which was dynamically cured alone and blended with PP and HDPE later (cure–blend). The effect of DCP concentration, intensity of the shear mixing, and rubber/plastics composition was studied. The tensile strength and modulus increased with increasing DCP concentration in the blends of EPDM-rich compositions but decreased with increasing DCP concentration in blends of PP-rich compositions. In the morphological analysis by scanning electron microscopy (SEM), the small amount of EPDM acted as a compatibilizer to HDPE and PP. It was also revealed that the dynamic curing process could reduce the domain size of the crosslinked EPDM phase. When the EPDM forms the matrix, the phase separation effect becomes dominant between the EPDM matrix and PP or HDPE domain due to the crosslinking in the matrix.     

Crystallization,melting behavior,and morphology of BPP/HDPE blend

The crystallization, melting behavior, and morphology of a low ethylene content block propylene–ethylene copolymer (BPP) and a high-density polyethylene (HDPE) blend were studied. It was found that the existence of ethylene–propylene rubber (EPR) in BPP has more influence on the crystallization of HDPE than on that of PP. This leads to the decreasing of the melting temperature of the HDPE component in the blends. It is suggested that the EPR component in BPP shifted to the HDPE component during the blending process. The crystallinity of the HDPE phase in the blends decreased with increasing BPP content. The morphology of these blends was studied by polarized light microscopy (PLM) and SEM. For a BPP-rich blend, it was observed that the HDPE phase formed particles dispersed in the PP matrix. The amorphous EPR chains may penetrate into HDPE particles to form a transition layer. © 1998 John Wiley & Sons, Inc. J. Appl. Polym. Sci. 69: 2469–2475, 1998     

Effect of Addition of HDPE and LDPE on Rheological,Mechanical, Elastic and Compatibility Behavior of SBR/NBR Rubber Blend System

The influence of adding low density polyethylene (LDPE) and high density polyethylene (HDPE) to different ratios of styrene butadiene copolymer (SBR) and acrylonitrile butadiene copolymer (NBR) rubber blend has been studied. The experimental methods performed are based on measurements of rheological, mechanical, elastic properties, phase morphology, density, ultrasonic studies, thermal stability and differential scanning calorimetry (DSC). Results showed that rheological and mechanical properties of the blend are improved, especially at SBR/NBR blend (50/50), when incorporated with LDPE. Results indicated also a clear stability of the cure rate index (CRI) of the blend. Morphological structure analysis obtained from scanning electron microscope (SEM) showed a reduced domain size for blends containing LDPE. Ultrasonic and density investigations revealed the efficiency of adding LDPE in improving the compatibility behavior of this blend. Results also showed an improvement in elastic properties and thermal stability by adding LDPE. DSC scans of the blends filled with LDPE showed high shift in the glass transition temperature which can be attributed to the increased strength at the interface.     

The effect of glycidyl methacrylate and styrene comonomers on compatibility,physical-mechanical properties,and swelling behavior of SBR/NBR blends

The effect of functionalized styrene-butadiene rubber (SBR) with glycidyl methacrylate (GMA) monomers, in the presence of styrene comonomers (SBR-g-GMA-co-St) as a compatibilizer on physical-mechanical, morphological, and swelling behavior of SBR/nitrile butadiene rubber (NBR) blends were studied. It was proved that the compatibilizer made through dicumyl peroxide-induced reaction which possessed 1.5 phr GMA in addition to 1.5 phr styrene comonomers showed higher efficiency of grafting. Possible in situ reactions between SBR-g-GMA-co-St and NBR component also were evaluated with an attenuated total reflectance mode of Fourier-transform infrared spectroscopy. SBR/NBR blend containing compatibilizer with a middle value of grafting demonstrated the most reactions between components. Dynamic mechanical thermal analysis results illustrated that the presence of SBR-g-GMA-co-St caused a significant improvement in compatibility of two components. This was verified with the scanning electron microscope pictures in which a smoother surface of the sample was clear. The enhancement in microstructure led to an increase in tensile strength, elongation at break, and storage modulus. Moreover, the increase in the intermolecular cross-links and made interactions considerably affected blends' swelling behavior in both hydrocarbon solvents (carbon tetrachloride and chloroform).     

Oil resistant thermoplastic elastomers of nitrile rubber and high density polyethylene blends

Different grades of oil resistant thermoplastic elastomers (TPE) based on blends of nitrile rubber (NBR) and high density polyethylene (HDPE) have been developed. Chemical treatment of HDPE to evolve compatibility with NBR and dynamic vulcanization with different curatives have been studied. Determination of physico‐mechanical and thermal properties and relative crystallinity of these blends have been carried out. Oil resistance characteristics of the blends have been evaluated in different commercially used oils and fuels for applications as a substitute for NBR/polyvinyl chloride (PVC) blends.     

Compatibilization of SBR/NBR Blends Using Poly Acrylonitrile as Compatibilizer

Blends of styrene-co-butadiene rubber (SBR) and acrylonitrile-co-butadiene rubber (NBR) were prepared and their rheological and mechanical properties were examined. The effect of the addition of 5 phr of poly acrylonitrile as compatibilizer on the compatibility of the rubber blend was studied. Ultrasonic and scanning electron microscopy (SEM) techniques were used to assess the degree of compatibility of the blend. The results revealed that the use of the prepared compatibilizer has significantly resulted in the clear stability of the cure rate index (CRI) of the blends and that the tensile strength was improved at (50/50) SBR/NBR blend. The degree of compatibility was enhanced to a great extent.     

High density polyethylene/acrylonitrile butadiene rubber blends: Morphology,mechanical properties,and compatibilization

Polymer blends based on high-density polyethylene (HDPE) and acrylonitrile butadiene rubber (NBR) were prepared by a melt blending technique. The mixing parameters such as temperature, time, and speed of mixing were varied to obtain a wide range of properties. The mixing parameters were optimized by evaluating the mechanical properties of the blend over a wide range of mixing conditions. The morphology of the blend indicated a two-phase structure in which NBR phase was dispersed as domains up to 50% of its concentration in the continuous HDPE matrix. However, 70 : 30 NBR/HDPE showed a cocontinuous morphology. The tensile strength, elongation at break, and hardness of the system were measured as a function of blend compostion. As the polymer pair is incompatible, technological compatibilization was sought by the addition of maleic-modified polyethylene (MAPE) and phenolic-modified polyethylene (PhPE). The interfacial activity of MAPE and PhPE was studied as a function of compatibilizer concentration by following the morphology of the blend using scanning electron micrographs. Domain size of the dispersed phase showed a sharp decrease by the addition of small amounts of compatibilizers followed by a leveling off at higher concentrations. Also, more uniformity in the distribution of the dispersed phase was observed in compatibilized systems. The tensile strength of the compatibilized systems showed improvement. The mechanical property improvement, and finer and uniform morphology, of compatibilized systems were correlated with the improved interfacial condition of the compatibilized blends. The experimental results were compared with the current theories of Noolandi and Hong. © 1995 John Wiley & Sons, Inc.     

HDPE／NBR共混物的性能和结构研究

通过熔融共混法制备了HDPE/NBR（NBR为丁腈橡胶）二元共混物和HDPE/NBR/HDPE-g-MAH（MAH为马来酸酐）三元共混物，研究了其力学性能和相态结构。结果表明：对于极性不同的二元共混体系，加入15%（质量含量，下同）的NBR即可行到冲击强度为712.2J/m、相态结构为平行排列的丝状共混物；对于加有相容剂HDPE-g-MAH的三元共混体系，尽管冲击强度达到845.9J/m，但此时NBR加入量为25%，且相容剂的制备工艺繁琐，质量不好控制。     

Toughened polyoxymethylene by polyolefin elastomer and glycidyl methacrylate grafted high‐density polyethylene

Ternary blends of polyoxymethylene (POM), polyolefin elastomer (POE), and glycidyl methacrylate grafted high density polyethylene (GMA‐g‐HDPE) with various component ratios were studied for their mechanical and thermal properties. The size of POE dispersed phase increased with increasing the elastomer content due to the observed agglomeration. The notched impact strength demonstrated a parabolic tendency with increasing the elastomer content and reached the peak value of 10.81 kJ/m² when the elastomer addition was 7.5 wt%. The disappearance of epoxy functional groups in the POM/POE/GMA‐g‐HDPE blends indicated that GMA‐g‐HDPE reacted with the terminal hydroxyl groups of POM and formed a new graft copolymer. Higher thermal stability was observed in the modified POM. Both storage modulus and loss modulus decreased from dynamic mechanical analysis tests while the loss factor increased with increasing the elastomer content. GMA‐g‐HDPE showed good compatibility between the POM matrix and the POE dispersed phase due to the reactive compatibilization of the epoxy groups of GMA and the terminal hydroxyl groups of POM. A POM/POE blend without compatibilizer was researched for comparison, it was found that the properties of P‐7.5(POM/POE 92.5 wt%/7.5 wt%) were worse than those of the blend with the GMA‐g‐HDPE compatibilizer. POLYM. ENG. SCI., 57:1119–1126, 2017. © 2017 Society of Plastics Engineers     

High‐density polyethylene/natural rubber blends filled with thermoplastic tapioca starch: Physical and isothermal crystallization kinetics study

High‐density polyethylene/natural rubber (HDPE/NR) blends filled thermoplastic tapioca starch was studied. In this blend system, thermoplastic starch (TPS) acted as an inert component, and the influence of TPS incorporation was studied in terms of tensile properties and crystallization kinetics. Tensile properties of the blends were affected by the addition of TPS particles, which reflects the incompatibility and lack of adhesion at the interface. The effect of TPS incorporation on the crystallization behavior of the HDPE/NR blends was also evaluated at different predetermined crystallization temperatures. The isothermal crystallization data obtained in this study were analyzed by using the Avrami equation. The Avrami exponent for HDPE/NR and HDPE/NR‐10% TPS blends varied around 2.0 and slightly decreased around 1.8 for HDPE/NR‐30% TPS, implying the nucleation process is heterogeneous and the crystal growth is 2D. J. VINYL ADDIT. TECHNOL., 22:191–199, 2016. © 2014 Society of Plastics Engineers     

Properties and morphology of oriented ternary blends of poly(ethylene terephthalate), high density polyethylene,and compatibilizing agent

Oriented blends of poly(ethylene terephthalate) (PET) and high density polyethylene (HDPE) with and without compatibilizing agent have been studied with regard to orientation temperature, stretch rate, extension ratio, mode of orientation, and blend composition. These oriented blends have been characterized using infrared spectroscopy and differential scanning calorimetry. The tensile and tensile impact properties were also investigated. The results show that blends with compatibilizer show strain hardening upon orientation, whereas the blend without compatibilizer does not strain harden upon orientation. The blends with less PET content have been difficult to orient. The morphology of these blends show fibril structure, highly oriented in the direction of stretch. Infrared measurements show that PET within the blend has undergone strain induced crystallization upon orientation. It has also been observed that the mechanical properties, such as the modulus and ultimate stress, show improvement upon orientation. Simultaneously stretched blends show better physical properties than sequentially oriented blends.     

Effect of maleic anhydride grafting on nanokaolinclay reinforced polystyrene/high density polyethylene blends

Nanofillers have revolutionized the field of polymer modification. Modification of polymer blends with nanofillers opens up a myriad of opportunities to develop materials of choice. Polystyrene (PS) and high density polyethylene (HDPE) are two widely used standard plastics. To generate high modulus and strength a PS rich blend of PS/HDPE (80/20) was selected and the blend was modified using low cost nanokaolin clay, a 1:1 alumina silicate. The effect of maleic anhydride grafted PS/PE as compatibilizer in this system was studied. The incorporation of the compatibilizer improves the mechanical properties. This can be correlated with better interfacial adhesion as evidenced by scanning electron microscopy. The optimum in these properties was obtained at a compatibilizer concentration of 10–15%. The composites were characterized byX‐ray diffraction, differential scanning calorimetric, and dynamic mechanical analyzer techniques. This study shows that kaolin can be used as potential modifier of PS/HDPE blend. POLYM. COMPOS. 2012. © 2012 Society of Plastics Engineers     

Blends of high density polyethylene and poly(l‐lactic acid): Mechanical and thermal properties

The blends of high‐density polyethylene (HDPE) and poly(l ‐lactic acid) (PLLA) were prepared by melt blending method in an extrusion mixer with a postextrusion blown film attachment. The ratios of HDPE/PLLA blends were taken as 100/0, 95/5, 90/10, 85/15, and 80/20. The 80/20 blend was further compatibilized by adding maleic anhydride‐grafted polyethylene in different ratios (up to 8 wt%). Based on the mechanical properties of the films, the compositions HDPE80 (80% HDPE and 20% PLLA) and HD80C4 (80% HDPE, 20% PLLA, and 4% compatibilizer) were found to be optimum and considered for further analysis. The thermal properties of these selected blends were investigated by means of thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA study revealed that the addition of the PLLA somewhat decreased the thermal stability of HDPE. DSC investigation showed that the blends were partially miscible only. X‐ray diffraction (XRD) analysis enlightened that the crystallinity of blends was slightly increased with addition of PLLA. Immiscibility of the two polymers was diminished in the presence of compatibilizer, as indicated by the scanning electron microscopy (SEM) of the blends. These partially biodegradable blends may be used for flexible packaging applications. POLYM. ENG. SCI., 54:2155–2160, 2014. © 2013 Society of Plastics Engineers     

Determination of the compatibility of NBR‐EPDM blends by an ultrasonic technique,modulated DSC,dynamic mechanical analysis,and atomic force microscopy

In this study, the compatibility of immiscible binary blends of acrylonitrile‐co‐butadiene rubber (NBR) and ethylene proplylene diene rubber (EPDM) was characterized by various analytical techniques. Ultrasonic velocity measurements were conducted on solution blends of NBR and EPDM in various blend ratios as well as with the addition of either chlorinated polethylene (CM) or chlorosulphonated polyethylene (CSM) as a compatibilizer. Without the compatibilizer, the ultrasonic velocity was observed to vary in an apparently sinusoidal way with variation in the blend ratio. The addition of a compatibilizer, however, resulted in a marked increase of the ultrasonic velocity and significant changes in the nature of the plots of velocity vs. composition. Various other parameters (e.g., temperature, solid content of the solution blends, and efficacy of the compatibilizer) were found to affect the relative ultrasonic velocity values. Thermal analysis by modulated differential scanning calorimetry (MDSC) indicated that the segmental immiscibility between NBR and EPDM, and the addition of the compatibilizer resulted in characteristic peak shifts of the individual rubbers to form a broad plateau. Measurements of the storage modulus (E′), loss modulus (E″), and tan δ properties by dynamic mechanical analysis (DMA) also showed distinctive changes. Atomic force microscopy (AFM) on the surface topography, phase images, and histogram plots of the vulcanizates of 50:50 NBR‐EPDM blends were also carried out to study the effect of compatibilization. POLYM. ENG. SCI., 45:1265–1276, 2005. © 2005 Society of Plastics Engineers     

Studies on high density polyethylene/polycarbonate blend system compatibilized with low density polyethylene grafted diallyl bisphenol A ether

Blends of a high density polyethylene (HDPE) matrix and a polycarbonate (PC) minor phase were investigated through their morphology, heat resistance, mechanical properties, crystallizing behavior, rheological measurement and especially the compatible effect of a compatibilizer: low density polyethylene grafted diallyl bisphenol A ether (LDPE-g-DBAE). The blends without compatibilizer exhibited a phase growth and no adhesive between the HDPE matrix and the dispersed phase. In the presence of 10% by weight of LDPE-g-DBAE as a compatibilizer, more fine particles and a dim phase interface were observed, and the blends showed a remarkable increase in heat distortion temperature and mechanical properties. The compatibilized blends possessed a high apparent viscosity as compared with the noncompatibilized ones. However, the apparent viscosity of the blends, with or without the compatibilizer, was lower than that of the neat HDPE and PC. Exploration by DSC found that the melting point and the crystallinity of HDPE in the blends decreased, and especially for the blends with the compatibilizer. These facts could be interpreted in terms of the efficient compatible effect of the LDPE-g-DBAE, which resulted from the interaction between the diallyl bisphenol A ether unit of LDPE-g-DBAE and polycarbonate, and the miscibility of the LDPE unit and HDPE.     

Rheological properties and crystalline structure of the dynamically cured EPDM and PP/HDPE ternary blends

The rheological properties and crystalline structure of the polyolefin ternary blends of EPDM/polypropylene/high density polyethylene were studied. Blends were prepared in a laboratory internal mixer by two different methods. In blend–cure process, blending and curing were performed simultaneously and EPDM was cured by dicumyl peroxide (DCP) in the presence of PP/HDPE under shear. The cure–blend was to cure EPDM alone first under shear (dynamic curing) and then mix the cured EPDM with PP and HDPE. The effect of DCP concentration, intensity of the shear mixing, and the rubber/plastic composition were studied using capillary rheometer and X-ray diffractometer. The PP-rich ternary blends showed the effect of the mechanooxidative degradation of PP by shear and peroxide. The melt viscosity increased with increasing DCP concentration in blends of EPDM-rich compositions. X-ray diffraction studies revealed that the inclusion of 25 wt % of linear EPDM in the PP/HDPE mixture for the PP-rich ternary blends changed the crystal structure of polypropylene component in the ternary blends. However, the dynamic curing did not alter the crystal structure of PP or HDPE in the blends.     

Dynamic mechanical properties and morphology of high‐density polyethylene/CaCO3 blends with and without an impact modifier

Dynamic mechanical analysis and differential scanning calorimetry were used to investigate the relaxations and crystallization of high‐density polyethylene (HDPE) reinforced with calcium carbonate (CaCO₃) particles and an elastomer. Five series of blends were designed and manufactured, including one series of binary blends composed of HDPE and amino acid treated CaCO₃ and four series of ternary blends composed of HDPE, treated or untreated CaCO₃, and a polyolefin elastomer [poly(ethylene‐co‐octene) (POE)] grafted with maleic anhydride. The analysis of the tan δ diagrams indicated that the ternary blends exhibited phase separation. The modulus increased significantly with the CaCO₃ content, and the glass‐transition temperature of POE was the leading parameter that controlled the mechanical properties of the ternary blends. The dynamic mechanical properties and crystallization of the blends were controlled by the synergistic effect of CaCO₃ and maleic anhydride grafted POE, which was favored by the core–shell structure of the inclusions. The treatment of the CaCO₃ filler had little influence on the mechanical properties and morphology. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3907–3914, 2007