The Effect of Triacetin on the Plasticization Efficiency and Tensile Properties of Polyvinyl Chloride/di-2-Ethyl Hexyl Phthalate/Triacetin Compounds

2016 ◽  
Vol 1133 ◽  
pp. 206-210 ◽  
Author(s):  
Arjulizan Rusli ◽  
Nur Farhana Asul Kahar
Keyword(s):  
Molecular Weight ◽  
Tensile Strength ◽  
Glass Transition ◽  
Tensile Properties ◽  
Polyvinyl Chloride ◽  
Chemical Structure ◽  
Low Molecular Weight ◽  
Migration Ability ◽  
Elongation At Break ◽  
Before And After

The use of triacetin as an alternative plasticizer to polyvinyl chloride (PVC) was studied in term of plasticizer efficiency and tensile properties before and after ageing. The efficiency of plasticizers was evaluated based on the glass transition temperature (Tg) and the hardness value of the compounds. The Tg and hardness of all PVC/DEHP/Triacetin compounds are lower than PVC/50DEHP and PVC/50Triacetin compounds indicating synergistic plasticisation effect between both DEHP and Triacetin within the PVC compounds. The low molecular weight and chemical structure of triacetin are believed to contribute to the highest tensile strength, elongation at break and modulus of the PVC/triacetin compared with PVC/DEHP and PVC/DEHP/triacetin compounds. However, the migration ability of the triacetin plasticizer is believed to result in the biggest changes of the tensile properties of PVC compounds plasticized with triacetin before and after ageing.

Processing, Thermal Behavior and Tensile Properties of PLA/Thermoplastic Starch/Montmorillonite Nanocomposites

2013 ◽  
Vol 684 ◽  
pp. 75-79
Author(s):  
Esmat Jalalvandi ◽  
Taravat Ghanbari ◽  
Hossein Cherghibidsorkhi ◽  
Ehsan Zeimaran ◽  
Hamid Ilbeygi
Keyword(s):  
Tensile Strength ◽  
Glass Transition ◽  
Thermal Properties ◽  
Transition Temperature ◽  
Thermal Behavior ◽  
Tensile Properties ◽  
Thermoplastic Starch ◽  
Screw Extruder ◽  
Elongation At Break ◽  
Twin Screw

Thermoplastic starch, polylactic acid glycerol and maleic anhydride (MA) were compounded with natural montmorillonite (MMT) through a twin screw extruder to investigate the effects of different loading of MMT on tensile properties and thermal behavior of the nanocomposites. Tensile results showed an increased in modulus, tensile strength and elongation at break. However, beyond 3phr of MMT the modulus of samples decreased because the MMT particles agglomerated. The thermal properties were characterized by using differential scanning calorimeter (DSC). The results showed that MMT increased melting temperature and crystallization temperature of matrix but reduction in glass transition temperature was observed.

EFFECT OF PLASTICIZER EXTRACTION BY JET FUEL ON A NITRILE HOSE COMPOUND

2015 ◽  
Vol 88 (2) ◽  
pp. 324-342 ◽  
Author(s):  
Richard J. Pazur ◽  
T. A. C. Kennedy
Keyword(s):  
Molecular Weight ◽  
Tensile Strength ◽  
Glass Transition ◽  
Chemical Structure ◽  
Jet Fuel ◽  
Butadiene Rubber ◽  
Maximum Torque ◽  
Lower Viscosity ◽  
Aromatic Components ◽  
Polymeric Plasticizer

ABSTRACT Seven ester plasticizers were evaluated in a reference acrylonitrile–butadiene rubber (NBR) fuel hose compound with respect to extractability resistance to jet fuel. Plasticizers differed primarily in chemical structure (polarity) and molecular weight (monomeric vs polymeric). Plasticizer addition led to lower viscosity, maximum torque, modulus, tensile strength, and enhanced low temperature properties. Exposure to jet fuel caused plasticizer extraction resulting in compound softening due to absorption of the aromatic components in the fuel. The glass transition temperature shifted toward lower temperatures. Extraction resistance is enhanced by optimizing polymer–plasticizer compatibility and by using a higher molecular weight plasticizer. The use of the polymeric plasticizer A-8600 lowers the loss of other fugitive plasticizers, indicating the presence of specific plasticizer–plasticizer interactions. Of the monomeric and polymeric plasticizers, trioctyl trimellitate and A-8600, respectively, display the best combination of plasticizing ability and extraction resistance.

Nanoarchitectonics Composites of Thermoplastic Starch and Montmorillonite Modified with Low Molecular Weight Polylactic Acid

2020 ◽  
Vol 20 (5) ◽  
pp. 2955-2963
Author(s):  
Peixian Li ◽  
Huimin Guo ◽  
Kaixiong Yang ◽  
Xiaoyan Yu ◽  
Xiongwei Qu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Polylactic Acid ◽  
Composite Films ◽  
Thermoplastic Starch ◽  
Nanocomposite Films ◽  
Low Molecular Weight ◽  
Elongation At Break ◽  
Starch Films

Nano montmorillonite (MMT) was modified by low molecular weight polylactic acid (PLA), then, the PLA modified MMT and raw MMT were added into thermoplastic starch (TPS) to prepare biodegradable nanocomposite films, respectively. For both nanocomposite films with raw MMT and modified MMT, the Tmax of degradation was enhanced and the mechanical properties were improved. The composite films containing 4 wt.% MMT displayed tensile strength of 5.06 MPa, approximately 1.4 times of that for the pure TPS films. The tensile strength of composite films containing 4 wt.% modified MMT is 6.74 MPa approximately 2 times of those for pure starch films. On the other hand, the composite film containing 4 wt.% modified MMT displayed elongation at break as high as 34.25%, which is 1.3 times of that of the pure starch film, while the composite films containing raw MMT had reduced elongation at break. This study showed that the MMT modified with PLA could significantly enhance the mechanical properties of TPS, and provides a new method to prepare fully biodegradable starch-based nanocomposites.

Ultimate Tensile Properties of Segmented Polyurethane Elastomers: Factors Leading to Reduced Properties for Polyurethanes Based on Nonpolar Soft Segments

1986 ◽  
Vol 59 (3) ◽  
pp. 405-431 ◽  
Author(s):  
T. A. Speckhard ◽  
S. L. Cooper
Keyword(s):  
Molecular Weight ◽  
Glass Transition ◽  
Phase Separation ◽  
Block Copolymers ◽  
Tensile Properties ◽  
Soft Segment ◽  
Low Molecular Weight ◽  
Polyurethane Elastomers ◽  
Soft Segments ◽  
Available Information

Abstract Factors that could explain the lower tensile properties of nonpolar soft-segment-based polyurethane block copolymers relative to those of conventional polyether or polyester polyurethanes have been examined. Many of the materials studied in the literature have suffered from the use of soft segments with poor functionality, which has led to low molecular weight, network defects, and an unfavorable amount of crosslinking. Additionally, most of the materials have been based on soft segments whose molecular weight appears to be too high to obtain optimum properties. Polyurethanes based on nonpolar soft segments are also likely to suffer from premature phase separation during polymerization leading to low molecular weight and compositional heterogeneity, especially if the reaction is done in bulk. The lower soft-segment glass-transition temperature of, in particular, the polydimethylsiloxane polyurethanes can also contribute to their lower tensile properties at room temperature. However, if differences in the soft-segment glass-transition temperatures are accounted for by comparing samples at equivalent values of T−Tg and other parameters are optimized, it appears that only a lack of soft-segment crystallizability under strain and possibly an excessively high degree of phase separation are inherently limiting the tensile properties of nonpolar soft-segment-based polyurethane block copolymers. The limited amount of available information concerning the effects of many of these factors suggests a need for additional work in this area.

Properties of Random PSF/PES Copolymers as High-Performance Polymers

2011 ◽  
Vol 217-218 ◽  
pp. 1606-1610
Author(s):  
Dong Jiang ◽  
Xiao Ran Zhang ◽  
Yan Mei Ma ◽  
Cheng You Ma
Keyword(s):  
Weight Loss ◽  
Tensile Strength ◽  
Glass Transition ◽  
High Performance ◽  
Molar Ratio ◽  
Transition Temperatures ◽  
Elongation At Break ◽  
Glass Transition Temperatures ◽  
High Performance Polymers ◽  
Diphenyl Sulfone

A series of random polysulfone/polyethersulfone (PSF/PES) copolymers were synthesized by the polycondensation of 4, 4'-isopropylidendiphenol, 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-dichlorodiphenyl sulfone in the presence of K2CO3. We obtained a series of copolymers by changing the molar ratio of 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-isopropylidendiphenol (it was marked as the ratio of S:A). The copolymers have the similar solubility with polyethersulfone. They also have high glass transition temperatures (Tg: 199°C~229°C) and 5% weight loss temperatures (4, 4'-isopropylidendiphenol: 4, 4΄-dihyolroxy diphenyl sulfone=1:1, Td5=497°C). At the same time the elongation at break is much higher than that of PES, while the tensile strength is a little lower than that of PES.

scholarly journals Characterisation of Sequential Solvent Fractionation and Base-catalysed Depolymerisation of Treated Alkali Lignin

BioResources ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. 4137-4151 ◽  
Author(s):  
Aikfei Ang ◽  
Zaidon Ashaari ◽  
Edi Suhaimi Bakar ◽  
Nor Azowa Ibrahim
Keyword(s):  
Molecular Weight ◽  
Chemical Structure ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Solubility Parameters ◽  
Low Molecular Weight ◽  
Sequential Fractionation ◽  
Weight Average Molecular Weight ◽  
Solvent Fractionation ◽  
Alkali Lignin

An alkali lignin (OL) with a weight-average molecular weight (Mw) of 11646 g/mol was used to prepare low-molecular weight lignin for resin synthesis. The low-molecular weight lignin feedstock was obtained via base-catalysed depolymerisation (BCD) treatments at different combined severity factors. Sequential fractionation of the OL and BCD-treated lignins using organic solvents with different Hildebrand solubility parameters were used to alter the homogeneity of the OL. The yield and properties of OL itself and OL and BCD-treated OL dissolved in propan-1-ol (F1), ethanol (F2), and methanol (F3) were determined. Regardless of the treatment applied, a small amount of OL was dissolved in F1 and F2. The BCD treatment did not increase the yield of F1 but did increase the yields of F2 and F3. Gel permeation chromatography (GPC) showed that the repolymerization reaction occurred in F3 for all BCD-treated OL, so these lignins were not suitable for use as feedstocks for resin production. The GPC, 13Carbon-nuclear magnetic resonance, and Fourier transform infrared spectroscopy analyses confirmed that the F3 in OL exhibited the optimum yield, molecular weight distribution, and chemical structure suitable for use as feedstocks for resin synthesis.

Tensile Properties of Polypropylene/Cocoa Pod Husk Biocomposites: Effect of Maleated Polypropylene

2013 ◽  
Vol 747 ◽  
pp. 645-648 ◽  
Author(s):  
Koay Seong Chun ◽  
Salmah Husseinsyah ◽  
Hakimah Osman
Keyword(s):  
Tensile Strength ◽  
Tensile Properties ◽  
Tensile Modulus ◽  
Melt Blending ◽  
Elongation At Break ◽  
Maleated Polypropylene ◽  
Matrix Interaction ◽  
Cocoa Pod Husk ◽  
Blending Process ◽  
Scanning Electron

Polypropylene/Cocoa Pod Husk (PP/CPH) biocomposites with different maleated polypropylene (MAPP) content were prepared via melt blending process using Brabender Plastrograph mixer. The tensile strength and tensile modulus of PP/CPH biocomposites increased with increasing of MAPP content. The PP/CPH biocomposites with 5 phr of MAPP showed the optimum improvement on tensile properties. However, the increased of MAPP content reduced the elongation at break of PP/CPH biocomposites. At 5 phr of MAPP content, PP/CPH biocomposites showed lowest elongation at break. Scanning electron microscope confirms the PP/CPH biocomposites with MAPP have better filler-matrix interaction and adhesion due to the effect of MAPP.

Synthesis of Cyclic Polysulfides and their Properties as Curing Agents

2004 ◽  
Vol 77 (2) ◽  
pp. 380-390
Author(s):  
Wonmun Choi ◽  
Tomoyuki Matsumura
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
High Molecular Weight ◽  
Mass Spectra ◽  
Elongation At Break ◽  
Molecular Weights ◽  
Aging Properties ◽  
Curing Agents ◽  
Polysulfide Polymer

Abstract The reactions of dichloroalkanes and sodium tetra-sulfide (Na2S4) were carried out in a mixture of water and toluene to produce corresponding cyclic polysulfides and polysulfide polymer. The low molecular weights of cyclic sulfides were obtained by the reaction at 90 °C, while the high molecular weight of polysulfide polymer was obtained by the reaction at 50 °C. GPC chromatograms and Mass spectra revealed that the structures of cyclic polysulfide were 1:1, 2:2, and 3:3 adducts of dichloroalkane and sodium tetra-sulfide. The mechanical properties of vulcanized NR at 148 °C with cyclic sulfides were similar to that with sulfur. However, both tensile strength and elongation at break of vulcanized NR at 170 °C with cyclic sulfides are much higher than that with sulfur. The aging properties of vulcanized NR at 148 °C or 170 °C with cyclic polysulfides indicate better stability.

scholarly journals The effects of alkanolamide addition on cure characteristics, swelling behaviour and tensile properties of silica-filled natural rubber (NR) / chloroprene rubber (CR) blends

2018 ◽  
Vol 34 ◽  
pp. 01030 ◽  
Author(s):  
Indra Surya ◽  
Syahrul Fauzi Siregar ◽  
Hanafi Ismail
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Tensile Properties ◽  
Crosslink Density ◽  
Tensile Modulus ◽  
Palm Stearin ◽  
Swelling Behaviour ◽  
Elongation At Break ◽  
Cure Characteristics ◽  
Chloroprene Rubber

Effects of alkanolamide (ALK) addition on cure characteristics, swelling behaviour and tensile properties of silica-filled natural rubber (NR)/chloroprene rubber (CR) blends were investigated. The ALK was synthesized from Refined Bleached Deodorized Palm Stearin (RBDPS) and diethanolamine, and incorporated into the silica-filled NR/CR blends as a non-toxic rubber additive. The ALK loadings were 0.0, 1.0, 3.0, 5.0 and 7.0 phr. It was found that the ALK exhibited shorter scorch and cure times and higher elongation at break of the silica-filled NR/CR blends. The ALK also exhibited higher torque differences, tensile modulus and tensile strength at a 1.0 phr of ALK loading and then decreased with further increases in the ALK loading. The swelling measurement proved that the 1.0 phr loading of ALK caused the highest degree in crosslink density of the silica-filled NR/CR blends.

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