Effect of trimethylolpropane triacrylate (TMPTA) on the properties of irradiated epoxidized natural rubber (ENR‐50), ethylene‐(vinyl acetate) copolymer (EVA), and an ENR‐50/EVA blend

The effect of trimethylolpropane triacrylate (TMPTA) monomer on the tensile properties, dynamic mechanical properties, and morphology of irradiated epoxidized natural rubber (ENR‐50), ethylene‐(vinyl acetate) copolymer (EVA), and an ENR‐50/EVA blend was investigated. The ENR‐50, EVA, and ENR‐50/EVA blend were irradiated by using a 3.0‐MeV electron‐beam apparatus at doses ranging from 20 to 100 kGy. The improvement of tensile properties and morphology with irradiation indicated the advantage of having irradiation‐induced crosslinks in these materials. Observation of the properties studied confirmed that TMPTA was efficient in enhancing the irradiation‐induced crosslinking of ENR‐50, EVA, and the ENR‐50/EVA blend. Addition of TMPTA improved the adhesion between the ENR‐50/EVA blend phases by forcing grafting and crosslinking at a higher irradiation dose (100 kGy). J. VINYL ADDIT. TECHNOL., 2009. © 2009 Society of Plastics Engineers.     

Physical properties of ethylene vinyl acetate copolymer (EVA)/natural rubber (NR) blend based foam

In this study an attempt was made to improve the rebound resilience and to decrease the density of ethylene‐vinyl acetate copolymer (EVA) foam. For this purpose, EVA was blended with natural rubber (NR), and EVA/NR blends were foamed at 155°C, 160°C, and 165°C. To investigate the correlation between crosslinking behavior and physical properties of foams, crosslinking behavior of EVA/NR blends was monitored. The physical properties of the foams were then measured as a function of foaming temperatures and blend compositions: 165°C was found to be the optimal temperature for a crosslinking of EVA/NR foam. As a result, the density of EVA/NR blend foamed at 165°C was found to be the lowest. EVA/NR (90/10) blend, foamed at 165°C, showed lower density, better rebound resilience, and greater tear strength than EVA foam. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2212–2216, 2004     

Effect of epoxidized natural rubber on thermal properties,fatigue life,and natural weathering test of styrene butadiene rubber/recycled acrylonitrile‐butadiene rubber (SBR/NBRr) blends

The utilization of waste rubber powder in polymer matrices provides an attractive strategy for polymer waste disposal. Addition of recycled acrylonitrile‐butadiene rubber (NBRr) in rubber compounds gives economic (lowering the cost of rubber compounds) as well as processing advantages. In this study, the properties of styrene butadiene rubber (SBR)/NBRr blends with and without epoxidized natural rubber (ENR‐50) as a compatibilizer were determined. The results such as thermal gravimetric analysis (TGA), fatigue life, and natural weathering test of SBR/NBRr blends with and without ENR‐50 were carried out. Results showed that TG thermograms of SBR/NBRr blends with ENR‐50 show lower thermal stability compared blends without ENR‐50. The incorporation of ENR‐50 into SBR/NBRr blends has reduced char residue compared SBR/NBRr blends without ENR‐50. The incorporation of ENR‐50 in SBR/NBRr blends has increased the rigidity of the blends thus lowering the fatigue life. The increment in tensile properties retention of SBR/NBRr blends with ENR‐50 indicated the enhancement on weathering resistant. The surfaces of SBR/NBRr blends with ENR‐50 after 6 months exposure showed a minimal severity of crack compared with SBR/NBRr blends without ENR‐50. It revealed that the scale of cracks has reduced indicating well‐retaining interfacial adhesion between SBR and NBRr with the presence of ENR‐50 as a compatibilizer. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A structural study of epoxidized natural rubber (ENR‐50) ring opening under mild acidic condition

A structural study of ring opening reaction of purified epoxidized natural rubber (ENR) with acetic acid was conducted using the NMR techniques and its thermal characteristic was evaluated with Thermal gravimetry/Differential Thermal Gravimetry (TG/DTG) and Differential Scanning Calorimetry (DSC) analyses. ¹H‐NMR revealed that 19.56% of epoxide was ring‐opened from the total amount of the epoxide unit in ENR‐50 and this was supported by Fourier Transform Infrared (FTIR) spectroscopy. ¹³C‐NMR suggests the fixation of alkyl (R) i.e., acetate group to the epoxide carbon via ester linkage and formation of hydroxyl groups in the polymer chains. The attachment location of R occurred at both most (↑) and least (↓) hindered carbons of the epoxide. The TG/DTG results of acid treated ENR‐50 showed three decomposition steps at 235–338, 338–523, 523–627 °C due to the presence of the polymer chains mixture, i.e., ring‐opened and intact epoxide of ENR‐50. This increases the T_g value of acid treated ENR‐50 at 24.6 °C as compared to purified ENR‐50 at −17.7 °C. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44123.     

Adhesion properties of (epoxidized natural rubber)/(ethylene‐propylene‐diene rubber) blend adhesive: Effect of blend ratio and testing rate

The adhesion properties of epoxidized natural rubber (ENR 25)/(ethylene‐propylene‐diene rubber) blend adhesive were investigated by using various blend ratios of the two rubbers and rate of testing. Coumarone‐indene resin was used as the tackifier. Results show that the loop tack and peel strength of adhesives increase steadily up to 60% ENR 25 before decreasing with further increase in % ENR 25. This observation is attributed to an increase in wettability and compatibility up to the optimum value of the ENR 25 blend ratio. However, shear strength increases continuously with increasing percentage of ENR 25, an observation that is ascribed to the increasing cohesive strength of the blend adhesive. In all cases, the adhesion properties increase with increasing coating thickness and testing rates. J. VINYL ADDIT. TECHNOL., 22:134–139, 2016. © 2014 Society of Plastics Engineers     

Orientation effects on the deformation and fracture properties of high‐density polyethylene/ethylene vinyl acetate (HDPE/EVA) blends

In this paper, the tensile deformation and fracture toughness of high‐density polyethylene (HDPE)/ethylene vinyl acetate (EVA) blends, obtained by dynamic packing injection moulding, have been comprehensively investigated in different directions of rectangle samples, including longitudinal, latitudinal and oblique directions relative to the flow direction. Two kinds of EVA were used with VA content 16 wt% (16EVA) and 33 wt% (33EVA) to control the interfacial interactions. The results indicate that molecular orientation and interfacial interaction play very important roles to determine the tensile behaviour and fracture toughness. Biaxial‐reinforcement of tensile strength was seen for HDPE/16EVA blends but only uniaxial‐reinforcement was observed for HDPE/33EVA blends. The difference is caused by the different interfacial interactions as highlighted by the peel test, scanning electron microscopy (SEM) observation as well as theoretical evaluation. Very high impact strength, decreasing with increasing EVA content, was observed when the fracture propagation is perpendicular to the shear flow direction, while a low impact strength, increasing slightly increasing with EVA content, was seen when the fracture propagation is parallel to the shear flow. The fracture of oblique samples is always along the flow direction instead of along the impact direction or tensile direction. The tensile behaviour and fracture toughness are discussed on the basis of the formation of transcrystalline zones, orientation of EVA particles and matrix toughness of HDPE in different directions. Copyright © 2004 Society of Chemical Industry     

Miscibility and adhesive properties of ethylene vinyl acetate copolymer (EVA)‐based hot‐melt adhesives. I. Adhesive tensile strength

A series of ethylene vinyl acetate copolymers (EVA) were blended with some tackifier resins that are made from wood extracts, and possible relations between their miscibility and properties as hot‐melt adhesives (HMA) were investigated. From our previous report on miscibility of various EVA‐based HMAs, we chose some blends that represent some of typical miscibility types and measured their adhesive tensile strengths. When the blends were miscible at testing temperatures, the temperature at which the maximum value of adhesive tensile strength was recorded tended to move toward higher temperature as tackifier content of blends increased. This result corresponds to the glass transition temperature (T_g) of the blends that became higher as tackifier content of blends increased when blend components were miscible. In terms of HMA performances, we suggest that factors other than miscibility affect absolute values of adhesive tensile strength more directly than miscibility; this idea has to be investigated further in a future study. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 719–725, 2002     

Organic vapor permeation through natural rubber/poly(ethylene‐co‐vinyl acetate) blend membranes

Natural rubber/poly(ethylene‐co‐vinyl acetate) (NR/EVA) blend membranes, crosslinked with dicumyl peroxide, have been prepared and tested for vapor permeation characteristics. The effects of structure and morphology of the blend membranes on the permeability were investigated. The permeability was found to decrease with increase in EVA content which has been attributed to the semicrystalline nature of EVA. The permeation process has been observed to be controlled mainly by the molecular mass of the penetrants. In the case of benzene/acetone mixtures, it has been found that when acetone concentration increases the vapor permeation rate decreases. This clearly indicates less interaction of acetone towards NR/EVA membranes. For supporting all the observations, the parameters such as swelling coefficient and permeability coefficient have been calculated. POLYM. ENG. SCI., 48:198–202, 2008.© 2007 Society of Plastics Engineers     

Thermal and chemical stabilization of ethylene/vinyl acetate/vinyl alcohol (EVA‐OH) terpolymers under nitroplasticizer environments

In this study, we compare the aging behaviors of cross‐linked ethylene/vinyl acetate/vinyl alcohol terpolymers, also referred to as EVA‐OH, when they are either immersed in nitroplasticizer (NP) liquid or exposed to NP vapor at different temperatures. While thermogravimetric analysis and differential scanning calorimetry are used to probe the thermal stability of aged NP and polymers, Fourier transform infrared, gel permeation chromatography, ultra‐violet/vis, and nuclear magnetic resonance are used to probe their structural changes over the aging process. The study confirms that NP degrades through C? N cleavage, and releases HONO molecules at a slightly elevated temperature (<75°C). As these molecules accumulate in the vapor phase, they react among themselves to create an acidic environment. Therefore, these chemical constituents in the NP vapor significantly accelerate the hydrolysis of EVA‐OH polymer. When the hydrolysis occurs in both vinyl acetate and urethane groups and the scission at the cross‐linker progresses, EVA‐OH becomes vulnerable to further degradation in the NP vapor environment. Through the comprehensive characterization, the possible degradation mechanisms of the terpolymers are proposed. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41450.     

The effect of an epoxidized plasticizer on the thermo-oxidative ageing of poly(vinyl chloride)/epoxidized natural rubber thermoplastic elastomers

The effects of an epoxidized plasticizer on the mechanical properties and thermo-oxidative ageing behaviour of poly(vinyl chloride)/epoxidized natural rubber thermoplastic elastomers (TPEs) were investigated. Aged and unaged blends were characterized by FTIR, tensile properties, tear strength, hardness and dynamic mechanical analysis (DMA). The properties of the epoxidized soya oil (ESO) plasticized TPEs were compared with those of the di-2-ethylhexylphthalate (DOP) plasticized counterparts. The presence of epoxide groups in ESO has been shown to produce two conflicting effects. On the one hand, the presence of excessive epoxide groups has resulted in poor ageing behaviour. On the other hand, it has resulted in a good interaction and compatibility with PVC/ENR. It was found that the tensile strength of the ESO plasticized blends were comparable with the DOP plasticized ones, but the elongation at break (EB) of the ESO blends fell short of that of the DOP blends. Also the retention of both tensile properties for the ESO blends was poorer than for DOP blends. Hardening and embrittlement also occurred in the ESO blends. Despite these weaknesses, ESO could be an ideal plasticizer for the PVC/ENR system as indicated by plasticizer permanence and the greater efficiency of plasticization. © 1998 SCI.     

Effect of electron‐beam irradiation on poly(vinyl chloride)/epoxidized natural rubber blend: dynamic mechanical analysis

The irradiation‐induced crosslinking in 50/50 poly(vinyl chloride)/epoxidized natural rubber (PVC/ENR) blend was investigated by means of dynamic mechanical analysis. The influence of trimethylolpropane triacrylate on the irradiation‐induced crosslinking of PVC/ENR blends was also studied. The enhancement in storage modulus and T_g with irradiation dose indicated the formation of irradiation‐induced crosslinks. This is further supported by the decrease in tan δ_max and loss modulus peak. The compatibility of the blend was found to be improved upon irradiation. The Fox model was used to provide a further insight into the irradiation‐induced compatibility in the blend. Scanning electron microscopy studies on the cryofracture surface morphology of the blends as well as the homopolymer have been undertaken in order to gain more evidence on the irradiation‐induced crosslinking. © 2001 Society of Chemical Industry     

Studies on polyamide‐6/polyolefin blend system compatibilized with epoxidized natural rubber

Infrared spectra of polyamide‐6 (PA6) with and without epoxidized natural rubber (ENR) are presented. The influence of ENR used as a compatibilizer on the morphologies, crystallizability, mechanical properties, and thermal behavior of the polyamide‐6/polyolefins (PO) blends are studied. The infrared spectra suggest that under normal processing conditions, the carboxyl end groups of PA6 could chemically react in situ with the epoxy groups of ENR, and ester groups are created. This means that the PA6‐ENR grafting copolymer could be obtained during processing. All the morphological characterizations and thermal analyses show that the compatibility of PA6/PO blends is obviously improved by ENR because the copolymer increases the interaction between PA6 and PO. It is also found that the toughness of PA6/PO blends increase significantly after using ENR, while the tensile strength and the softening temperature of PA6/PO blends have almost no change. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 398–403, 2003     

Effect of rubber content on mechanical properties and heat shrinkage of ethylene vinyl acetate copolymer blended with epoxidized natural rubber

Ethylene vinyl acetate (EVA, 18 mol % vinyl acetate) and epoxidized natural rubber (ENR, 50 mol % epoxidation) were blended in an internal mixer and compared to EVA. Dicumyl peroxide (DCP) was used as a curing agent. The blends consisted of 10–50 wt % of ENR and were compared with crosslinked EVA in terms of heat shrinkage, mechanical properties, and degree of crystallinity. It is found that the blends showed a decrease in mechanical properties with increasing ENR content because DCP was not a good vulcanizing agent of ENR. The addition of ENR did not affect heat shrinkability of EVA. The maximum heat shrinkage obtained was 80% for EVA and the blends. ENR did not affect thermal properties of EVA investigated by the differential scanning calorimetry. The X‐ray diffractometry showed discrepancy in degree of crystallinity before and after specimen stretching and after heat shrinking. It is believed that ENR particles decreased molecular orientation of EVA resulting in a decrease in degree of crystallinity but the remained orientation was sufficient for heat shrinking. The blend showed better extrudability than EVA after increasing take‐up speed. Therefore, the extruded tube prepared from the blend provided higher heat shrinkage than EVA tube. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of different curing systems on heat shrinkability and mechanical properties of ethylene vinyl acetate/epoxidized natural rubber blends

Ethylene vinyl acetate (EVA)/epoxidized natural rubber (ENR) blends containing 10 and 30 wt % ENR were prepared by using an internal mixer. Five different types of curing systems were employed: dicumyl peroxide (DCP), sulfur (S), phenolic resin (Ph), DCP + S, and DCP + Ph. DCP could crosslink with both EVA and ENR while S and Ph were curing agents for ENR. The DCP system provided the lowest tensile properties and tear strength because of low crosslinking in ENR phase. Addition of sulfur or phenolic resin increased the mechanical properties due to a better vulcanization of the rubber phase. The mechanical properties of the blends decreased with increasing ENR content. The rubber particle size in the blends containing 30% ENR played a more important role in the mechanical properties than the blends containing 10% ENR. ENR particle size did not affect heat shrinkability of EVA and a well vulcanized rubber phase was not required for high heat shrinkage. Furthermore, heat shrinkage of the blends slightly changed as the ENR content increased for all curing systems. With regard to the mechanical properties and heat shrinkability, the most appropriate curing system was DCP + Ph and in the case the 10 wt % ENR content produced a more favorable blend. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effects of epoxidized natural rubber (ENR‐50) and processing parameters on the properties of NR/EPDM blends using response surface methodology

The effects of epoxidized natural rubber (ENR‐50) and processing parameters on the properties of natural rubber/ethylene–propylene–diene rubber (NR/EPDM; 70 : 30 phr) blends were studied. The compounds were prepared by melt compounding method. Using response surface methodology of two‐level full factorial, the effects of ENR‐50 contents (?1 : 5 phr; +1 : 10 phr), mixing temperature (?1 : 50°C; +1 : 110°C), rotor speed (?1 : 40 rpm; +1 : 80 rpm), and mixing time (?1 : 5 min; +1 : 9 min) in NR/EPDM blends were evaluated. Cure characteristics and tensile properties were selected as the responses. The significance of factors and its interaction was analyzed using ANOVA and the model's ability to represent the system was confirmed using the constant of determination, R² with values above 0.90. It was found that the presence of ENR‐50 has the predominant role on the properties of NR/EPDM blends. The addition of ENR‐50 significantly improved cure characteristics and tensile strength up to 5.12% and 6.48% compared to neat NR/EPDM blends, respectively. These findings were further supported by swell measurement, differential scanning calorimetry, and scanning electron microscopy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40713.     

Preparation of ethylene vinyl acetate (EVA) copolymer nanotubes by wetting of anodic alumina oxide (AAO) method

Ethylene vinyl acetate (EVA) nanotube arrays were successfully prepared through wetting of anodic alumina oxide (AAO) template with polymer melt or solution, a simple physical technique. The results of scanning electron microscope (SEM) demonstrate that the wall thickness of nanotubes via solution wetting method varies from the concentrations of solutions. The EVA nanotubes, obtained from 5.0 to 7.0 wt% EVA solutions, are ca. 40 nm and ca. 60 nm, respectively. As for melt wetting method, the length of nanotubes depends on temperature and the flow properties of polymer melt. The mechanism of forming the nanotubes has been also discussed.     

Thermomechanical properties and shape memory effect of epoxidized natural rubber crosslinked by 3‐amino‐1,2,4‐triazole

A thermally induced shape memory polymer based on epoxidized natural rubber (ENR) was produced by curing the ENR with 3‐amino‐1,2,4‐triazole as a crosslinker in the presence of bisphenol‐A as a catalyst. Dynamic mechanical and tensile analysis was conducted to examine the variation of glass transition temperature, stiffness, and extensibility of the vulcanizates with the amount of curatives. Shape memory properties of the ENR vulcanizates were characterized by shape retention and shape recovery. It was revealed that the glass transition temperature of the ENR vulcanizates could be tuned well above room temperature by increasing the amount of curing agents. Also, ENR vulcanizates with T_g higher than ambient temperature showed good shape memory effects under 100% elongation, and the response temperatures of the recovery were well matched with T_g of the samples. Copyright © 2006 Society of Chemical Industry     

Solid‐state NMR and morphological studies of poly(ethylene‐co‐vinyl acetate)/poly(vinyl acetate) blends

To obtain a correlation among structure–morphology–mobility–compatibility properties of poly(ethylene‐co‐vinyl acetate) (EVA)/poly(vinyl acetate) (PVAc) blends, we have used scanning electron microscopy and solid‐state nuclear magnetic resonance in our investigations. The results are discussed in terms of blends, component dispersion, plasticization effect, and domain mobilities to acquire a response of the correlation between structural properties. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2990–2996, 1999     

Mechanical and sorption properties of poly(ethylene-co-vinyl acetate)(EVA) compatibilized acrylonitrile butadiene rubber/natural rubber blend systems

Poly (ethylene-co-vinyl acetate) (EVA) has been used as a compatibilizer for heterogeneous natural rubber/acrylonitrile butadiene rubber (NR/NBR) blends. NR/NBR (50/50) blends were compatibilized with varying amounts, from 0 to 10 parts per hundred rubber (phr), of EVA. The compatibility of the blend components in presence of EVA has been evaluated in terms of mechanical and sorption characteristics. The mechanical properties were found to be improved by the addition of EVA upto 6 phr. The solvent resistance of the compatibilized samples has been observed to be higher compared to the uncompatibilized blends; attributed to the increased interfacial adhesion between the blend components. DSC studies showed a shift of glass transition temperatures of the blend components towards higher temperatures indicating increased rigidity of the matrix in presence of EVA.     

Fabrication and characterization of HCl‐treated clinoptilolite filled ethylene vinyl acetate composite films

As received and HCl treated Clinoptilolite (C)‐ethylene vinyl acetate (EVA) composites were prepared via the melt‐mixing technique, and extruded through a single‐screw extruder to obtain composite strips with an average thickness of 0.5 mm. The films were then characterized for their morphological, structural, thermal, and mechanical properties. Optical micrographs show that at higher C loading, the particles form large agglomerates, resulting in the formation of voids on the surface of the films. With increasing zeolite loading, the films become brittle, resulting in reduced Young's modulus. Acid treatment of the C tends to affect the crystal structure of the zeolite, resulting in poor tensile properties of the HCl‐treated zeolite‐filled EVA films. Addition of the zeolite also increased the crystallinity of the structure, acting as a nucleating agent in the EVA crystallization. Modeling of the tensile yield data with Pukanszky model indicate that there is poor interfacial adhesion between the polymer matrix and the filler particles. Thermal characterization studies showed that addition of the zeolites retarded the onset degradation temperature of EVA. However, degradation temperatures including T_max and the final decomposed temperature were increased, suggesting improved thermal stability due to reduced inter‐chain mobility in the composite materials as a result of increased zeolite loading. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013