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     

Flame retardant flexible poly(vinyl chloride) compound for cable application

ZnO/MgO, ZnO/CaO, and ZnO/CaO/MgO can form solid solutions. The solid solution for we as flame retardant (SSFR) was obtained by annealing at 1023 K for 4.5 h in a muffle furnace. Flexible poly (vinyl chloride) (PVC) filled with SSFR and Sb₂O₃ was investigated by differential thermal analysis thermogravimetry. Limiting oxygen index (LOI), mechanical properties, and electrical properties were studied. The surface of the char formed after combusting of the PVC compounds was observed through scanning electron microscopy and the effect of the surface area to the LOI was also studied. The data suggested that a small amount of SSFR and Sb₂O₃ have good synergy and can greatly increase the LOI and the char yield, and that the thermal degradation temperature and the activation energy decreased. It can be concluded that the mechanism of SSFR is a condensed‐phase mechanism. Moreover, one can conclude that the surface area can enhance the LOI. All the results showed that SSFR is effective and safe as a flame retardant in flexible PVC. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3137–3142, 2003     

Behavior of flexible poly(vinyl chloride)/poly(hydroxybutyrate valerate) blends

Blends of flexible poly(vinyl chloride) (PVC) and a poly(hydroxybutyrate valerate) (PHBV) copolymer were prepared and characterized with different techniques. The tensile strength of PVC did not show a marked reduction at PHBV concentrations up to 50 phr, despite a lack of miscibility between the two polymers. The crystallization of the PHBV copolymer was markedly hindered by the presence of PVC, as calorimetric results revealed. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and characterization of flexible poly(vinyl chloride) foam films

In this study, the effect of activator ZnO and heating time at 190°C on foaming, gelation, and dehydrochlorination of poly(vinyl chloride) (PVC) plastisol was investigated. For this purpose, a PVC plastisol was prepared by mixing PVC, dioctyl phthalate (DOP), azodicarbonamide (ADC), ZnO, and the heat stabilizers calcium stearate (CaSt₂) and zinc stearate(ZnSt₂). PVC plastisol films were heated for 3, 6, 12, and 24 min periods at 190°C to see the effect of heating time on the gelation and foaming processes of the PVC foam. The time of 12 min was determined to be optimum for the completion of gelation and foaming processes without thermal degradation of PVC. No foaming was observed under the same conditions for the samples without ZnO. ZnO had a significant catalytic effect on ADC decomposition, accelerating the foaming of the films. Average porosity measurement showed a consistent increase in porosity with heating time up to 76% and the average density decreased from 1.17 to 0.29 g/cm³ on foaming. Tensile tests showed that the tensile strength and tensile strain both increased considerably up to 0.98 MPa and 207%, respectively, with heating time and the elastic modulus was seen to gradually decrease from 4.7 to 0.7 MPa with heating time. Films without ZnO had higher tensile strength since there were no pores. PVC thermomat tests showed that ZnO lowered the stability time of plastigel film with azodicarbonamide. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Improved falling weight impact test for poly(vinyl chloride) products

A modified impact test using a 6.35 millimeter diameter tapered impacting tool has been developed to test profiles above 2.5 millimeters in thickness. The new method also helps to find the ductile-brittle transition easily. It is even more important for the prediction of toughness, especially for exterior applications, than the minimum energy required for any type of failure.     

The solubility of vinyl chloride in poly(vinyl chloride)

The solubility of vinyl chloride monomer (VCM) in PVC powders has been studied by equilibrium vapor pressure and microbalance gravimetric techniques at temperatures from 30 to 110°C. At temperatures and VCM concentrations above the glass transition, the solubility closely follows the Flory-Huggins equation with χ = 0.98 and is independent of temperature and of the PVC type, molecular weight, or history. In the glassy state, the VCM solubility is higher than the Flory-Huggins value and shows pronounced dependence upon time and the PVC history. These results have been interpreted through the dual-mode sorption concept of Michaels, Vieth, and Barrie: Normal dissolution follows the Flory-Huggins relation, and the additional glassy-state solubility represents the contribution of a hole-filling process. Changes in solubility with time and sample history parallel well-known volume relaxation processes, indicating that vapor solubility measurements offer a direct and sensitive measure of the free-volume state of glassy polymers.     

Improvements to C-ring fracture toughness test for poly(vinyl chloride) pipes

Abstract

Examination of the published procedure for performing calculations on data obtained from the C-ring fracture toughness test for unplasticised poly(vinyl chloride) reveals a major flaw. The dimensions of the specimens do not satisfy the ASTM criteria for plane strain conditions and correction factors are therefore introduced. However, there is an error in the calculation procedure, which results in variations in the severity of the test with pipe wall thickness. An improved approach is proposed and recommendations are made for changing the ISO/DIS 11673·2 test standard, to allow for variations in the yield strength of unplasticised poly(vinyl chloride) and to identify the calculated data as K _c rather than K _1c.     

Processing aids for poly(vinyl chloride)

Processing aids are an important class of additives for poly(vinyl chloride) (PVC). At relatively low concentration, processing aids enable the melt processing of rigid PVC and enlarge its processing windows. Discussed in this presentation are some major functions of processing aids, such as promoting PVC fusion, modifying PVC's melt rheology, and lubricating to prevent adherence of PVC melt to the processing equipment. Some examples are given to show the effects of processing aids on PVC die swell, melt fracture, melt viscosity, and PVC fusion. Commercial sources of various processing aids and typical PVC formulations for various applications are also discussed.     

Polymeric costabilisers for poly(vinyl chloride)

Methacrylate-based copolymers with 2-hydroxyethyl methacrylate and 2,3-epoxypropyl methacrylate, respectively, were synthesised and investigated as costabilisers for PVC. It was found that these polymers are capable of improving the induction time of PVC dehydrochlorination. This costabilising effect is dependent on the amount of functional groups which have been introduced into the copolymer. The new costabilisers interact with most used kinds of stabilisers and are capable of partly substituting the metal stabilisers.     

Modification of poly(vinyl chloride). XIX. Electroplating of poly(vinyl chloride)

As a preliminary treatment in the PVC-electroplating procedure, treatment with dimethylformamide followed by sensitization leads to a finely roughened and a highly hydrophilic surface with reducing power. This is caused by the formation of an ionic complex compound between dimethylformamide and tin(II) chloride absorbed in the PVC surface. A much more finely and deeply etched surface which exhibits higher adhesion through the mechanical interlocking effect is obtained with the PVC blends containing the plasticizer with a low value of interaction parameter and with a solubility parameter approximate to that of PVC. Adhesion of the metal layer to the PVC surface thus obtained is improved about 1.5 times by thermal aging at 120°C for 20 min.     

Automated microscopic technique for evaluating poly(vinyl chloride)–plasticizer compatibility

An automated microtechnique has been developed that permits a rapid, reproducible determination of the Flory–Huggins χ interaction parameters for poly(vinyl choloride)–plasticizer systems. It is a modification of the Anagnostopoulos method of determining an apparent melting temperature of a poly(vinyl chloride) (PVC) particle in excess plasticizer. A microscope equipped with a photodiode sensor is used to measure changes in the light transmitted through a plasticizer sample containing a PVC particle as the temperature is increased at a fixed rate, either 0.2 or 1.0°C/min. Data acquisition is done by computer so that minimal operator assistance is required. The apparent melting region is characterized by a sigmoidal change in the light transmitted through a fixed sample area. This curve allows an accurate, reproducible definition of the apparent melting temperature from which the χ parameter is easily derived. The values obtained for the interaction parameter of PVC with four plasticizers chosen from the phthalate and phosphate families are in good agreement with general trends of solvent quality. Separate experiments demonstrated that the overall transmittance profile reflects changes in both the size and the optical clarity of the PVC particle during heating. This leads to added features in the profile that reflect important diffusion and swelling characteristics for a given system. © 1994 John Wiley & Sons, Inc.     

Studies of electrical properties of some fire-retarding poly(vinyl chloride) compositions

Several fire-resistant formulations were prepared from a sample of poly(vinyl chloride) (PVC), small variable proportions of chloroorganic adducts [1,2,3,4,7,7-hexachloro-5-carboxy,bicyclo(2,2,1)heptene-2] or [1,2,3,4,7,7-hexachloro-5-carboxy,5-methyl-bicyclo(2,2,1)heptene-2] as fire-retarding modifiers, plasticizers (dibutylphthalate and a chlorinated paraffin), and a heat stabilizer (dibutyltindilaurate). The fire-resistance and electrical properties of the obtained formulations were studied to obtain a fire-retarding plasticized PVC of good electrical insulation character. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 27–35, 1997     

Degradation of poly(vinyl chloride)

The decomposition of poly(vinyl chloride) below 155°C has been examined by thermogravimetric analysis. Degradation is enhanced by irradiation with 1 MeV electrons. Later stages of isothermal weight loss for thermal and radiolytic decomposition follow 3/2-order kinetics and a similar reaction scheme is inferred. A free radical mechanism for dehydrochlorination involving allyl and polyenyl radicals is postulated.     

Dehydrochlorination of poly(vinyl chloride)

PVC has been dehydrochlorinated with alcoholic alkali in soution at 7°C for different lengths of time. At early stages of dehydrochlorination the dominant reaction is intramolecular removal of HCl and this gives rise to two intense Raman bands at ～ 1126 (ν₁) and ～ 1518 cm^?1 (ν₂) and following UV irradiation, to a quadruplet ESR spectrum. Increasing polyene sequence length and intermolecular removal of HCl at later stages of reaction alters the quadruplet signal to a singlet, shifts ν₁ and ν₂ to lower frequencies and increases the molecular weight. The presence of polyene units stiffens the chain and increases the elastic modulus. The T_g is, however, lowered slightly due to the removal of bulky chlorine atoms which relieves steric hindrance and dipole interaction between neighboring chains. The β-transition is also rendered less distinct.     

Miscibility in poly(vinyl chloride)/chlorinated poly(vinyl chloride) blends,and blends of different chlorinated poly(vinyl chlorides)

Blends of poly(vinyl chloride) with chlorinated poly(vinyl chloride) (PVC), and blends of different chlorinated poly(vinyl chlorides) (CPVC) provide an opportunity to examine systematically the effect that small changes in chemical structure have on polymer-polymer miscibility. Phase diagrams of PVC/CPVC blends have been determined for CPVC's containing 62 to 38 percent chlorine. The characteristics of binary blends of CPVC's of different chlorine contents have also been examined using differential calorimetry (DSC) and transmission electron microscopy. Their mutual solubility has been found to be very sensitive to their differences in mole percent CCl₂ groups and degree of chlorination. In metastable binary blends of CPVC's possessing single glass transition temperatures (T_g) the rate of phase separation, as followed by DSC, was found to be relatively slow at temperatures 45 to 65° above the T_g of the blend.     

Chemically crosslinked poly(vinyl chloride)

The effect of mixing time, temperature, and thermal treatment on mechanical properties of crosslinked PVC is investigated. The tensile properties and gel content of crosslinked and uncrosslinked PVC molded samples are evaluated. The cured samples exhibited higher tensile strength and thermal stability than unmodified PVC.     

Wet poly(vinyl chloride) membrane

Wet, porous, and semipermeable poly(vinyl chloride) (PVC) membrane prepared from a binary system, PVC and dimethylformamide, by immersing in alcohols or ethers was studied. The pore dimensions of the wet PVC membrane were from 0.01 to 0.05 μm, calculated from hydrodynamic permeability by using experimental values such as water flux and water content. They agreed reasonably well with the dimension of the pores which prevented the protein passing through the membrane, observed by SEM photographs. Formation of the wet PVC membrane can be explained by slow phase separation and slow leaching of the casting solution immersed in alcohols and ethers such as methanol and ethylene glycol monomethyl ether.     

Modelling and optimization of a flexible poly(vinyl chloride) compound formulation for mine cables

Developments by Labuschagné et al. (Patent, WO 2006/123284 A2, 2006) in the manufacture of Layered Double Hydroxides (LDHs) have led to a patent describing a new effluent free synthesis method. A promising application for the LDH is as an additive for a flexible poly(vinyl chloride) (PVC) compound used for the insulation for cables used in South African underground mines. Consequently, a new formulation is required. Unfortunately formulating a PVC compound is a complex problem. The purpose of the investigation is to develop a method that can be used to find an optimum PVC formulation where the material requirements are met while also allowing for the quantitative analysis of the effect of the ingredients on the material properties. This is achieved by modeling the thermal stability, fire retardancy, and basic mechanical properties of the compound as a function of the relative proportions of the ingredients using 2nd order Scheffé polynomials. The empirical models are determined using statistical experimental design. Each model is interpreted using statistical analysis of the model terms which allows for the quantification of the effects and interactions of all the ingredients on the various response variables. The models are also used as constraints in the optimization of the PVC formulation for minimum cost. Parametric analyses are done to demonstrate how the optimization can be used to analyze the entire system taking into account the cost performance of the ingredients. Finally, it is demonstrated how the above approach requires significantly less time and labor to find an optimum formulation than the traditional approach. J. VINYL ADDIT. TECHNOL., 25:E44–E58, 2019. © 2017 Society of Plastics Engineers     

Rheology of poly(vinyl chloride) dry blends I. A fusion model for evaluating rigid dry blend compound performance

This study of rigid poly(vinyl chloride) (PVC) dry blend fusion proceeds via scanning electron microscope (SEM) examination of material in a sigma mixing bowl fitted torque rheometer. A mathematical model is developed and tested. During the course of the study, degradation behavior was observed some time before the conventional t₂ or the end point of thermal stability. A suitable model for torque changes during degradation was not developed.