Studies of electrical and mechanical properties of semiconductive poly(vinyl chloride) compositions

A sample of poly(vinyl chloride) (PVC) and a polar plasticizer consisting of dioctylphthalate (DOP) and triisopropylphenylphosphate (TIPPP) was prepared and found to possess some electrical conductivity. Different samples of PVC compositions were formulated from the PVC-DOP-TIPPP system and also variable proportions of the conductive materials polyaniline or the Ni salt of ethylene glycol bisadipate ester. Dibutyltindilaurate as a heat stabilizer, titanium oxide as a filler, and sandorin red 20 pigment were added. The effect of the structure of polyaniline and Ni adipate ester on the electrical and mechanical properties of the PVC–DOP–TIPPP system was studied to obtain a semiconductive plasticized PVC with good mechanical properties. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 685–693, 1998     

Studies of electrical and mechanical properties of poly(vinyl chloride) mixed with electrically conductive additives

Different samples of poly(vinyl chloride) (PVC) compositions were formulated from PVC, a polar plasticizer such as dioctylphthalate (DOP), and variable proportions of electrically conductive additives such as fast extrusion furnace (FEF) carbon black (CB), poly(vinylpyridine) (PVP), or polyacrylonitrile (PAN). Epoxidized soybean oil was added as a heat stabilizer. Samples of the PVC–CB system were also prepared by dispersing different concentrations of CB into the PVC matrix. The electrical studies showed that the addition of CB to the PVC–DOP system produces a plasticized PVC with high electrical conductivity whereas the compounding of PVC with CB produces a sample with much higher electrical conductivity. The effect of the structure of PVP and PAN on the electrical and mechanical properties of the PVC–DOP system was also studied to obtain a semiconductive plasticized PVC with good mechanical properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1590–1598, 2004     

Design and fabrication of flexible poly(vinyl chloride) dielectric composite reinforced with ZnO microvaristors

Flexible poly(vinyl chloride)/varistor composites were fabricated by solution casting method. High‐field ZnO varistor particles processed from micron‐sized Zn dust is explored as multifunctional filler for PVC composites. Mechanical blending of Zn dust with La₂O₃‐CeO₂ rare earths and varistor forming minor additives followed by sintering at 1250 °C resulted in fine‐grained ZnO varistors. Bulk varistor was subsequently milled to obtain ZnO microvaristor grains. The effect of microvaristor on the UV stability, dielectric, and mechanical properties of the PVC composite was analyzed. The varistor filler in PVC enhanced the microhardness and retained the tensile properties without any significant loss. After UV irradiation PVC/varistor composite shows remarkable mechanical stability retention (95%) compared to pure PVC (75%). Also, microvaristor reinforcement resulted in dielectric constant tunability (? = 2–37) without any drastic change in the dielectric loss (0.02–0.05). Thus, Zn dust‐derived ZnO varistors could be potentially exploited to design functional PVC composites for electronic applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46031.     

Evaluation of the effects of biobased plasticizers on the thermal and mechanical properties of poly(vinyl chloride)

Blends were prepared of poly(vinyl chloride) (PVC) with four different plasticizers; esters of aconitic, citric, and phthalic acids; and other ingredients used in commercial flexible PVC products. The thermal and mechanical properties of the fresh products and of the products after 6 months of aging were measured. Young's modulus of the PVC blends was reduced about 10‐fold by an increase in the plasticizer level from 15 to 30 phr from the semirigid to the flexible range according to the ASTM classification, but a 40‐phr level was required for PVC to retain its flexibility beyond 6 months. At the 40‐phr level, tributyl aconitate performed better than diisononyl phthalate (DINP) or tributyl citrate, in terms of lowering Young's modulus, both in the fresh materials and those aged for 6 months. The effects of the four plasticizers on the glass‐transition temperature (T_g) were similar, with T_g close to ambient temperature at the 30‐ and 40‐phr levels in freshly prepared samples and at 40–60°C in those aged for 6 months. The thermal stability of the PVC plasticized with DINP was superior among the group. Overall, tributyl aconitate appeared to be a good candidate for use in consumer products where the alleged toxicity of DINP may be an issue. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1366–1373, 2006     

Experimental investigations of polypropylene and poly(vinyl chloride) composites filled with plerospheres

Plerospheres, defined here as superfine spherical particles (0.5–5 μm) separated from fly ash (rather than as other solid spherical particles, as some have used the term), are separated from coal fly ash but are dramatically different from it. Plerospheres can be used as polymer fillers to improve the properties of composites. With plerospheres used as fillers for polypropylene (PP) and unplasticized poly(vinyl chloride) (UPVC), the effects of the filler content, the particle sizes of the plerospheres, and the coupling agent on the composite properties were studied. The particle sizes of the plerospheres were 2 and 5 μm. The results suggested that the notched impact properties both at a normal temperature and a low temperature and the tensile and flexural properties of plerosphere/PP increased significantly when the content was increased from 0 to 30 wt % and further increased with the addition of a coupling agent. Differential scanning calorimetry indicated that the thermal properties of the plerosphere/PP composite improved. The surface characteristics and morphology of the impact fracture surface were examined in detail with scanning electron microscopy. The rheological performance of plerosphere/UPVC pipe composites obviously improved; the plasticizing time was shortened, and the maximum torque was reduced. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 126–131, 2004     

Effect of the fiber content and plasticizer type on the rheological and mechanical properties of poly(vinyl chloride)/green coconut fiber composites

A series of poly(vinyl chloride) (PVC)/green coconut fiber (GCF) composites, with dioctyl phthalate (DOP) or thermoplastic polyurethane (TPU) as a plasticizer, were prepared by melt mixing. Their properties were studied in the molten state with an advanced nonlinear harmonic testing technique; in the solid state, the hardness and impact resistance were evaluated, and scanning electron microscopy was used for fractured surfaces. The effect of the fiber loading was investigated, as well as the role of the plasticizer. PVC–GCF composites are heterogeneous materials that, in the molten state, exhibit essentially a nonlinear viscoelastic character, in contrast to pure PVC, which has a linear viscoelastic region up to 50–60% strain. The complex modulus increases with the GCF content but in such a manner that the observed reinforcement is at best of hydrodynamic origin, without any specific chemical (i.e., permanent) interaction occurring between the polymer matrix and the fibers. As expected, PVC offers good wetting of GCFs, as reflected by the easy mixing and the rheological and mechanical properties. Fibers can be incorporated into PVC up to a 30% concentration without any problem, with the PVC/plasticizer ratio kept constant. Higher GCF levels could therefore be considered. Replacing DOP in part with TPU gives some benefit in terms of impact resistance, likely because of the viscoelastic nature of the latter and the associated energy absorption effects. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Effect of plasticizers on mechanical,electrical, permanence,and thermal properties of poly(vinyl chloride)

Effects of three different plasticizers and their blends with dioctyl phthalate (DOP) on thermal stability, flammability, mechanical, electrical, and permanence properties of poly(vinyl chloride) (PVC) compound were studied. Various plasticizers used were DOP, butyl benzyl phthalate (BBP), isodecyl diphenyl phosphate (IDDP), and polybutylene adipate (PBA) at concentrations of up to 40 phr level. Studies showed that processability and softness were improved by addition of BBP. An increase in the content of IDDP increased the electrical and flammability properties, whereas compositions with PBA exhibited the best permanence properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3278–3284, 2003     

Synthesis and properties of fluorescent light‐emitting polyamide hybrids with reactive nanosilica by epoxide functionalization

A series of poly(carbazole‐quinoxaline‐amide)s (PCQAs) containing phenyl and long alkyl chain as pendants was synthesized from polycondensation between a new diamine with a synthesized and several commercial dicarboxylic acids using Yamazaki's method. PCQAs had inherent viscosities and weight average molecular weights ( ) in the range of 0.48–0.62 dL g^?1 and 51,600–58,500 g mol^?1, respectively. These luminescent polymers are readily soluble in a variety of organic solvents and formed low‐colored and tough thin films. In this study, silane modified SiO₂ (mSiO₂) nanoparticles were prepared, characterized and used with PCQAs in preparation of nanocomposites via solution blending method. The interfacial interaction strength between mSiO₂ and the polymer–matrix enhanced thermal stability (T_10%, from 463°C to 500°C) and mechanical strength (from 100 MPa to 150 MPa) for composite containing 30 wt % mSiO₂ in comparison with the pure polyamide. These materials showed good ability for extraction–elimination of metal ions such as Cr⁶⁺, Cr³⁺, Co²⁺, Zn²⁺, Pb²⁺, Cd²⁺, and Hg²⁺ from aqueous solutions either individually or in the mixture at various pH. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40219.     

Preparation and properties of some filled poly(vinyl chloride) compositions

Different samples of filled poly(vinyl chloride) (PVC) compositions were formulated from PVC, a polar plasticizer mixture consisting of dioctylphthalate (DOP) and a chlorinated paraffin, and variable proportions of a white filler such as barite, calcium carbonate, kaoline, quartz, or talc; a conductive filler such as High Abrasion Furnace (HAF) carbon black; or a hydrated mineral filler such as aluminium hydroxide, magnesium hydroxide, or calcium hydroxide. Epoxidized soybean oil as a heat stabilizer and sandorin red (BRN) pigment were added. Electrical and mechanical studies show that the incorporation of white fillers produces a plasticized PVC of good electrical insulation character whereas the addition of HAF carbon black produces a sample with some electrical conductivity; both of them have good mechanical properties. Of the hydrated fillers studied aluminium hydroxide has been found to impart the best fire retardancy and good electrical properties for electric wires and cables. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2657–2670, 1999     

Mechanical properties of poly(vinyl chloride) blends and corresponding graft copolymers

The mechanical properties of the poly (vinyl chloride) (PVC) and poly (glycidyl methacrylate) [poly (GMA)] blend system and the PVC and poly (hydroxyethyl methacrylate) [poly (HEMA)] blend system and their crosslinked films were investigated. At the same time, the mechanical properties for the corresponding graft copolymers such as PVC-g-GMA, PVC-g-HEMA, and their crosslinked films were also investigated in this study. The results showed that the tensile strengths for PVC–poly (GMA) blend systems were higher than those for PVC-g-GMA graft copolymer, and the tensile strengths for PVC-g-HEMA were higher than those for PVC-poly (HEMA) blend systems. However, the mechanical properties for the PVC–poly (GMA) blend system were not affected by the crosslinking of the blend system, but those for PVC-poly (HEMA) and their graft copolymers decreased with an increase of the equivalent ratio ([NCO]/[OH]) of the crosslinker. Finally, the surface hydrophilicity of the PVC-g-HEMA graft copolymer and PVC-poly (HEMA) blends were also assessed through measuring the contact angle. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 67: 307–319, 1998     

A new biobased plasticizer for poly(vinyl chloride) based on epoxidized cottonseed oil

The use of epoxidized cottonseed oil as plasticizer for poly(vinyl chloride) was studied. The plasticizer content was set to 70 phr and the optimum isothermal curing conditions were studied in the temperature range comprised between 160 and 220 °C with varying curing times in the 7.5–17.5 min range. The influence of the curing conditions on overall performance of cured plastisols was followed by the evolution of mechanical properties (tensile tests with measurements of tensile strength, elongation at break, and modulus), change in color, surface changes of fractured samples by scanning electron microscopy (SEM), thermal transitions by differential scanning calorimetry, and migration in n‐hexane. The optimum mechanical features of cured plastisols are obtained for curing temperatures in the 190–220 °C range. For these curing conditions, fractography analysis by SEM gives evidences of full curing process as no PVC particles and free plasticizer can be found. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43642.     

Modification of poly(vinyl chloride) by IPN formation with poly(ethyl acrylate)

Semi‐1 and semi‐2 interpenetrating polymer networks (IPNs) of poly(vinyl chloride) (PVC) and in situ formed poly(ethyl acrylate) (PEA) have been synthesized using diallyl phthalate and ethylene glycol dimethacrylate as the crosslinkers of PVC and PEA, respectively. These two types of IPNs have been compared with respect to their physical, mechanical, and thermal properties and an endeavor has been made to find a correlation of these properties with the morphology generated in these systems. The semi‐1 IPNs displayed a decrease in their tensile strength and modulus while in contrast; the semi‐2 IPNs exhibited a marginal increase with increasing crosslinked PEA incorporation. The semi‐1 and semi‐2 IPNs containing 10 and 30 wt % of PEA displayed a two‐stage degradation typical of PVC in their thermogravimetric and DSC studies while confirming the increased stability of the samples with higher percentages of PEA. The softening characteristics as detected by the extent of penetration of the thermomechanical probe as has been detected by thermomechanical analysis are in conformity with their mechanicals. The biphasic cocontinuous systems as explicit from the morphological studies reveal fibrillar characteristics in both the systems. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Thermal and dynamic mechanical behavior of poly(vinyl chloride)/wood flour composites

Thermal and dynamic mechanical behaviors of wood plastic composites made of poly vinyl chloride (PVC) and surface treated, untreated wood flour were characterized by using differential scanning calorimetry and dynamic mechanical analysis. Glass transition temperature (T_g) of PVC was slightly increased by the addition of wood flour and by wood flour surface treatments. Heat capacity differences (ΔC_p) of composites before and after glass transition were markedly reduced. PVC/wood composites exhibited smaller tan δ peaks than PVC alone, suggesting that less energy was dissipated for coordinated movements and disentanglements of PVC polymer chains in the composites. The rubbery plateaus of storage modulus (E′) curves almost disappeared for PVC/wood composites in contrast to a well defined plateau range for pure PVC. It is proposed that wood flour particles act as “physical crosslinking points” or “pinning centers” inside the PVC matrix, resulting in the absence of the rubbery plateau and high E′ above T_g. The mobility of PVC chain segments were further retarded by the presence of surface modified wood flour. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Environmentally friendly plasticizers for poly(vinyl chloride)—Improved mechanical properties and compatibility by using branched poly(butylene adipate) as a polymeric plasticizer

Linear and branched poly(butylene adipate)s (PBA) with molecular weights ranging from 2000 to 10,000 g/mol, and a branching agent content between 0 and 1.8%, were solution cast with poly(vinyl chloride) (PVC) to form 50‐ to 60‐μm thick flexible films. Dry films were analyzed by tensile testing, Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and optical microscopy (OM) to study the effects of molecular weight and branching on the plasticizing efficiency of the polyester. PBA formed a semimiscible two‐phase system with PVC, where the amorphous part exhibited a single glass transition temperature. The degree of crystallinity for the polyester, surface composition, and mechanical properties of the films depended on the blend composition, molecular weight, and degree of branching of the polyester. Plasticizing efficiency was improved by higher degree of branching. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2180–2188, 2006     

Poly(vinyl chloride)/metallic oxides/organically modified montmorillonite nanocomposites: Preparation,morphological characterization,and modeling of the mechanical properties

Poly(vinyl chloride), metallic oxides (from copper, molybdenum, and zinc), and organically modified montmorillonite (O‐MMT) nanocomposites were prepared in a melt‐blending or intercalation‐in‐the‐molten‐state process. The morphology of the nanocomposites was evaluated with X‐ray diffraction (XRD) and transmission electron microscopy (TEM). Properties, such as the mechanical, thermal, and electrical properties, and the dynamic thermal stability against dehydrochlorination were also evaluated. Nanocomposites with a hybrid intercalated/exfoliated structure were obtained in all of the situations considered, as demonstrated by the XRD and TEM results and indirectly by the increment of Young's modulus of the formulations with increasing amount of O‐MMT incorporated. The modeling of Young's modulus by the Halpin–Tsai, Hui–Shia, and Lewis–Nielsen theories showed that the process of nanocomposite preparation allowed the aspect ratio of the clay particles to increase; these values were comparable to those nanocomposites obtained by other researchers with different polymeric matrices and methodologies. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Blends of poly(vinyl chloride) with acrylonitrile-chlorinated polyethylene-styrene copolymer. II. Mechanical properties

Blends of poly(vinyl chloride) (PVC) and acrylonitrile-chlorinated polyethylene-styrene (ACS) graft copolymer were prepared by melt blending. Mechanical properties were studied by the use of dynamic mechanical analysis (DMA), impact tests, tensile tests, and scanning electron microscopy (SEM). The DMA study showed that PVC is immiscible with chlorinated polyethylene in ACS but partially miscible with poly(styrene-co-acrylonitrile) (25% acrylonitrile content) in ACS. Mechanical property tests showed that there is a significant increase in the impact strength while other good mechanical properties of PVC such as high modulus and high strength remain. SEM observations supported the results of the mechanical properties studies. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 399–405, 1997     

Mechanochemical improvement of the flame‐retardant and mechanical properties of zinc borate and zinc borate–aluminum trihydrate‐filled poly(vinyl chloride)

In this study, the effect of the high‐energy mechanical milling of a mixture of poly(vinyl chloride) (PVC) with zinc borate (ZB) or ZB–aluminum trihydrate (ATH), a mixture of ZB and ATH, on the flame‐retardant and mechanical properties of ZB and ZB–ATH filled PVC was examined. The high‐energy mechanical milling of PVC/ZB and the PVC/ZB–ATH mixture produced chemical bonding between PVC and ZB or ZB–ATH, increasing the interfacial interaction of PVC/ZB and PVC/ZB–ATH blends, which resulted in a great increase in the limiting oxygen index, the impact and yield strengths, and the elongation at break of PVC/ZB and PVC/ZB–ATH blends. The results from ultraviolet spectroscopy and gas chromatography–mass spectroscopy show that mechanochemical modification of ZB and ZB–ATH much more effectively suppressed the release of aromatic compounds in PVC/ZB and PVC/ZB–ATH blends during burning. Mechanochemical modification provided an excellent route for the improvement of the flame‐retardant and mechanical properties of flame‐retardant‐additive‐filled PVC. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 753–762, 2003     

Blends of plasticized poly(vinyl chloride) and waste flexible poly(vinyl chloride) with waste nitrile rubber powder

Blends of poly(vinyl chloride) (PVC) with varying contents of plasticizer and finely ground powder of waste nitrile rubber rollers were prepared over a wide range of rubber contents through high‐temperature blending. The effects of rubber and plasticizer (dioctyl phthalate) content on the tensile strength, percentage elongation, impact properties, hardness, abrasion resistance, flexural crack resistance, limiting oxygen index (LOI), electrical properties, and breakdown voltage were studied. The percentage elongation, flexural crack resistance, and impact strength of blends increased considerably over those of PVC. The waste rubber had a plasticizing effect. Blends of waste plasticized PVC and waste nitrile rubber showed promising properties. The electrical properties and LOI decreased with increasing rubber and plasticizer content. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1552–1558, 2004     

Mechanical properties,flame retardancy,and smoke suppression of lanthanum organic montmorillonite/poly(vinyl chloride) nanocomposites

A dimethyl dioctadecyl ammonium chloride modified organic montmorillonite (OMMT_‐I.44P)/poly(vinyl chloride) (PVC) nanocomposite and anionic‐surfactant‐modified lanthanum organic montmorillonite (La‐OMMT)/PVC nanocomposites (with three different anionic surfactants for the La‐OMMTs) were prepared via melt‐intercalation technology. The effects of the La‐OMMTs and OMMT_‐I.44P on the mechanical properties, flame retardancy, and smoke suppression of PVC were studied. X‐ray diffraction characterization showed that the La‐OMMTs were exfoliated in the PVC matrix. The mechanical properties of the nanocomposites were enhanced by the incorporation of the La‐OMMTs. Cone calorimetry and gas chromatography–mass spectrometry analyses indicated that the incorporation of the La‐OMMTs enhanced the flame retardancy and smoke suppression of the PVC nanocomposites. Scanning electron microscopy photos further showed that the residual char surfaces of La‐OMMT/PVC were all intact and, thus, provided better barriers to energy and smoke transport. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43951.     

Peroxide crosslinking of rigid poly(vinyl chloride)

The optimum conditions for crosslinking rigid poly(vinyl chloride) with trimethylolpropane trimethacrylate (TMPTMA) and peroxide have been examined. The extent of crosslinking was measured by determining gel content by Soxhlet extraction in tetrahydrofuran. Mechanical properties were measured at 130°C and dynamic viscoelastic measurements were carried out to detect changes in the glass transition temperature (T_g). It was found that 15 phr of TMPTMA and 0.3 phr of peroxide were optimum concentrations for maximizing the extent of crosslinking, tensile strength, and T_g. The lower molding temperature of 170°C was preferred to minimize thermal degradation. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2904–2909, 2007