Phase Behavior and Properties of Polyurethane-PVC Blends and Fibers

1999 ◽  
Vol 72 (4) ◽  
pp. 587-601 ◽  
Author(s):  
Zoran S. Petrović ◽  
Ivan Javni ◽  
Jonathan Shull ◽  
Alan Waddon
Keyword(s):  
Thermomechanical Analysis ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Polyurethane Elastomer ◽  
Scanning Calorimetry ◽  
Polyester Urethane ◽  
Elastomeric Matrix ◽  
Low Concentrations ◽  
Rigid Poly ◽  
High Degree

Abstract A polyester urethane elastomer is blended with rigid poly(vinyl chloride) (PVC) and the miscibility of the components studied over the entire range of compositions. The polyurethane elastomer was a block copolymer with a low degree of crystallinity, while PVC was practically amorphous. Differential scanning calorimetry (DSC), thermomechanical analysis (TMA) and dynamic mechanical analysis (DMA) methods showed that polyester urethanes were partially miscible with PVC since two distinct glass transitions, which changed with the change of concentration of components, were observed. Although the PVC content was varied from 0–100%, the aim of the work was to examine if PVC at low concentrations would form fibrils in the urethane matrix and act as a reinforcing agent for the polyurethane elastomer. The morphology of the blends was studied by scanning electron microscopy and x-ray scattering. The blends were then spun into fibers to force the dispersed phase to elongate and form fibrils (draw ratio was about 100). A high degree of miscibility is obtained at low concentration of either of the components. The PVC phase in fibers spun from the blends have higher glass-transition temperature (Tg) than in isotropic blends, presumably due to increased orientation. No fibrillation of the rigid phase in the elastomeric matrix could be observed. The fibers displayed higher strengths but lower elongation at break than the isotropic blends of the same composition. Intermeshing morphology (at about 50/50 concentration) gave the lowest strengths.

scholarly journals Preparation and Characterization of Talc Filled Thermoplastic Polyurethane/Polypropylene Blends

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Emi Govorčin Bajsić ◽  
Vesna Rek ◽  
Ivana Ćosić
Keyword(s):  
Thermal Properties ◽  
Thermoplastic Polyurethane ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Polypropylene Blends ◽  
Pp Blends ◽  
The Degree Of Crystallinity ◽  
Better Than

The effect of the addition of talc on the morphology and thermal properties of blends of thermoplastic polyurethane (TPU) and polypropylene (PP) was investigated. The blends of TPU and PP are incompatible because of large differences in polarities between the nonpolar crystalline PP and polar TPU and high interfacial tensions. The interaction between TPU and PP can be improved by using talc as reinforcing filler. The morphology was observed by means of scanning electron microscopy (SEM). The thermal properties of the neat polymers and unfilled and talc filled TPU/PP blends were studied by using dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The addition of talc in TPU/PP blends improved miscibility in all investigated TPU/T/PP blends. The DSC results for talc filled TPU/PP blends show that the degree of crystallinity increased, which is due to the nucleating effect induced by talc particles. The reason for the increased storage modulus of blends with the incorporation of talc is due to the improved interface between polymers and filler. According to TGA results, the addition of talc enhanced thermal stability. The homogeneity of the talc filled TPU/PP blends is better than unfilled TPU/PP blends.

scholarly journals Application of Differential Scanning Calorimetry (DSC) and Modulated Differential Scanning Calorimetry (MDSC) in Food and Drug Industries

Polymers ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 5 ◽  
Author(s):  
César Leyva-Porras ◽  
Pedro Cruz-Alcantar ◽  
Vicente Espinosa-Solís ◽  
Eduardo Martínez-Guerra ◽  
Claudia I. Piñón-Balderrama ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Heat Capacity ◽  
Thermomechanical Analysis ◽  
Mechanical Analysis ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Modulated Differential Scanning Calorimetry ◽  
Accuracy And Precision ◽  
Wide Range ◽  
Transition Issues

Phase transition issues in the field of foods and drugs have significantly influenced these industries and consequently attracted the attention of scientists and engineers. The study of thermodynamic parameters such as the glass transition temperature (Tg), melting temperature (Tm), crystallization temperature (Tc), enthalpy (H), and heat capacity (Cp) may provide important information that can be used in the development of new products and improvement of those already in the market. The techniques most commonly employed for characterizing phase transitions are thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), thermomechanical analysis (TMA), and differential scanning calorimetry (DSC). Among these techniques, DSC is preferred because it allows the detection of transitions in a wide range of temperatures (−90 to 550 °C) and ease in the quantitative and qualitative analysis of the transitions. However, the standard DSC still presents some limitations that may reduce the accuracy and precision of measurements. The modulated differential scanning calorimetry (MDSC) has overcome some of these issues by employing sinusoidally modulated heating rates, which are used to determine the heat capacity. Another variant of the MDSC is the supercooling MDSC (SMDSC). SMDSC allows the detection of more complex thermal events such as solid–solid (Ts-s) transitions, liquid–liquid (Tl-l) transitions, and vitrification and devitrification temperatures (Tv and Tdv, respectively), which are typically found at the supercooling temperatures (Tco). The main advantage of MDSC relies on the accurate detection of complex transitions and the possibility of distinguishing reversible events (dependent on the heat capacity) from non-reversible events (dependent on kinetics).

scholarly journals Photocatalytic and adsorption properties of TiO2-pillared montmorillonite obtained by hydrothermally activated intercalation of titanium polyhydroxo complexes

2018 ◽  
Vol 9 ◽  
pp. 364-378 ◽  
Author(s):  
Mikhail F Butman ◽  
Nikolay L Ovchinnikov ◽  
Nikita S Karasev ◽  
Nataliya E Kochkina ◽  
Alexander V Agafonov ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Nitrogen Adsorption ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
New Approach ◽  
Pillared Montmorillonite ◽  
Degussa P25 ◽  
Adsorption Desorption ◽  
High Degree

We report on a new approach for the synthesis of TiO2-pillared montmorillonite, where the pillars exhibit a high degree of crystallinity (nanocrystals) representing a mixture of anatase and rutile phases. The structures exhibit improved adsorption and photocatalytic activity as a result of hydrothermally activated intercalation of titanium polyhydroxo complexes (i.e., TiCl4 hydrolysis products) in a solution with a concentration close to the sol formation limit. The materials, produced at various annealing temperatures from the intercalated samples, were characterized by infrared spectroscopy, differential scanning calorimetry (DSC)/thermogravimetric analysis (TGA), X-ray diffraction, dynamic light scattering (DLS) measurements, and liquefied nitrogen adsorption/desorption. The photocatalytic activity of the TiO2-pillared materials was studied using the degradation of anionic (methyl orange, MO) and cationic (rhodamine B, RhB) dyes in water under UV irradiation. The combined effect of adsorption and photocatalysis resulted in removal of 100% MO and 97.5% RhB (with an initial concentration of 40 mg/L and a photocatalyst-sorbent concentration of 1 g/L) in about 100 minutes. The produced TiO2-pillared montmorillonite showed increased photocatalytic activity as compared to the commercially available photocatalyst Degussa P25.

scholarly journals Review of Recent Developments of Glass Transition in PVC Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4336
Author(s):  
Jolanta Tomaszewska ◽  
Tomasz Sterzyński ◽  
Aneta Woźniak-Braszak ◽  
Michał Banaszak
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Thermomechanical Analysis ◽  
Mechanical Analysis ◽  
Temperature Dependent ◽  
Scanning Calorimetry ◽  
Recent Developments ◽  
Dielectric Thermal Analysis ◽  
The Impact

This review addresses the impact of different nanoadditives on the glass transition temperature (Tg) of polyvinyl chloride (PVC), which is a widely used industrial polymer. The relatively high Tg limits its temperature-dependent applications. The objective of the review is to present the state-of-the-art knowledge on the influence of nanofillers of various origins and dimensions on the Tg of the PVC. The Tg variations induced by added nanofillers can be probed mostly by such experimental techniques as thermomechanical analysis (TMA), dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), and dielectric thermal analysis (DETA). The increase in Tg is commonly associated with the use of mineral and carbonaceous nanofillers. In this case, a rise in the concentration of nanoadditives leads to an increase in the Tg due to a restraint of the PVC macromolecular chain’s mobility. The lowering of Tg may be attributed to the well-known plasticizing effect, which is a consequence of the incorporation of oligomeric silsesquioxanes to the polymeric matrix. It has been well established that the variation in the Tg value depends also on the chemical modification of nanofillers and their incorporation into the PVC matrix. This review may be an inspiration for further investigation of nanofillers’ effect on the PVC glass transition temperature.

scholarly journals Influence of the Lignin Content on the Properties of Poly(Lactic Acid)/lignin-Containing Cellulose Nanofibrils Composite Films

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1013 ◽  
Author(s):  
Xuan Wang ◽  
Yuan Jia ◽  
Zhen Liu ◽  
Jiaojiao Miao
Keyword(s):  
Lactic Acid ◽  
Lignin Content ◽  
Cellulose Nanofibrils ◽  
Composite Films ◽  
Tensile Tests ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Poly Lactic Acid ◽  
Scanning Calorimetry

Poly(lactic acid) (PLA)/lignin-containing cellulose nanofibrils (L-CNFs) composite films with different lignin contents were produced bythe solution casting method. The effect of the lignin content on the mechanical, thermal, and crystallinity properties, and PLA/LCNFs interfacial adhesion wereinvestigated by tensile tests, thermogravimetric analysis, differential scanning calorimetry (DSC), dynamic mechanical analysis, Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The tensile strength and modulus of the PLA/9-LCNFs (9 wt % lignin LCNFs) composites are 37% and 61% higher than those of pure PLA, respectively. The glass transition temperature (Tg) decreases from 61.2 for pure PLA to 52.6 °C for the PLA/14-LCNFs (14 wt % lignin LCNFs) composite, and the composites have higher thermal stability below 380 °C than pure PLA. The DSC results indicate that the LCNFs, containing different lignin contents, act as a nucleating agent to increase the degree of crystallinity of PLA. The effect of the LCNFs lignin content on the PLA/LCNFs compatibility/adhesion was confirmed by the FTIR, SEM, and Tg results. Increasing the LCNFs lignin content increases the storage modulus of the PLA/LCNFs composites to a maximum for the PLA/9-LCNFs composite. This study shows that the lignin content has a considerable effect on the strength and flexibility of PLA/LCNFs composites.

Thermal, morphological and mechanical properties of composites based on polyamide 6 with cellulose, silica and their hybrids from rice husk

2020 ◽  
pp. 002199832097829
Author(s):  
Renato P Melo ◽  
Marcelo P da Rosa ◽  
Paulo H Beck ◽  
Lucas GP Tienne ◽  
Maria de Fátima V Marques
Keyword(s):  
Mechanical Properties ◽  
Rice Husk ◽  
Natural Fibers ◽  
Polyamide 6 ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Cellulosic Fibers ◽  
The One ◽  
Properties Of Composites

The use of cellulosic fibers from different natural sources as fillers in polymer matrices to improve their properties has been extensively studied in the last years. It is mainly due to the vast availability of natural fibers as well as their biodegradability. The purpose of this present work was to extract cellulose, silica, and cellulose-silica fillers – these last called “hybrids” – from rice husk through delignification and subsequent oxidation and, then, prepare composites with polyamide 6 and improve mainly its thermal-mechanical properties. The content of 10 wt.% of fillers was inserted in PA 6 matrix. Infrared spectroscopy pointed the main characteristic peaks of cellulose and silica of hybrids, as thermogravimetric analysis showed high thermal stability of fillers, allowing their incorporation in PA-6 matrix by extrusion method. Thermo dynamic-mechanical analysis showed, in a general overview, a significant improvement of mechanical properties of composites, as elastic modulus, compared with neat polyamide-6, mainly the one with 2.5 wt% of silica and 7.5% of cellulose. This last also showed increasing of degree of crystallinity, measured by differential scanning calorimetry, showing the extraction efficiency of fillers from rice husk as well as the potential application of composites as structural components in automotive parts.

scholarly journals Thermal analysis of postcured aramid fiber/epoxy composites

2021 ◽  
Vol 60 (1) ◽  
pp. 479-489
Author(s):  
Konstantinos Karvanis ◽  
Soňa Rusnáková ◽  
Ondřej Krejčí ◽  
Alena Kalendová
Keyword(s):  
Thermal Resistance ◽  
Elevated Temperatures ◽  
Volume Fraction ◽  
Thermomechanical Analysis ◽  
Mechanical Analysis ◽  
Aramid Fiber ◽  
Point Of View ◽  
Creep Recovery ◽  
Aramid Fibers ◽  
Scanning Calorimetry

Abstract In this study, aramid fiber-reinforced polymer (AFRP) composites were prepared and then postcured under specific heating/cooling rates. By dynamic mechanical analysis, the viscoelastic properties of the AFRP composites at elevated temperatures and under various frequencies were determined. Thermomechanical analysis (TMA), in the modes of creep-recovery and stress–relaxation tests, was also performed. Furthermore, differential scanning calorimetry was also used, and the decomposition of the AFRP composites, aramid fibers, and pure postcured epoxy, in two different atmospheres, namely, air atmosphere and nitrogen (N2) atmosphere, was explored by the thermogravimetric analysis (TGA). From this point of view, the aramid fibers showed remarkably thermal resistance, in N2 atmosphere, and the volume fraction of fibers (Φf) was calculated to be Φf = 51%. In the TGA experiments, the postcured AFRP composites showed very good thermal resistance, both in air and N2 atmosphere, and this characteristic in conjunction with their relatively high T g, which is in the range of 85–95°C, depending on the frequency and the determination method, classifies these composites as potential materials in applications where the resistance in high temperatures is a required characteristic.

Formulations, development and characterization techniques of investment casting patterns

2019 ◽  
Vol 35 (3) ◽  
pp. 335-349 ◽  
Author(s):  
Robert K. Tewo ◽  
Hilary L. Rutto ◽  
Walter Focke ◽  
Tumisang Seodigeng ◽  
Lawrence K. Koech
Keyword(s):  
Investment Casting ◽  
Manufacturing Sector ◽  
Dimensional Accuracy ◽  
Casting Process ◽  
Thermomechanical Analysis ◽  
Mechanical Analysis ◽  
Filler Materials ◽  
Scanning Calorimetry ◽  
Investment Casting Process ◽  
Printed Patterns

Abstract Conventionally, unfilled wax has been used as a universal pattern material for the investment casting process. With increase in demand for accurate dimensions and complex shapes, various materials have been blended with wax to develop more suitable patterns for investment casting in order to overcome performance limitations exhibited by unfilled wax. The present article initially reviews various investigations on the development of investment casting patterns by exploring pattern materials, type of waxes and their limitations, the effect of filler materials and various additives on unfilled wax, wax blends for pattern materials, plastics and polymers for pattern materials and 3D-printed patterns. The superiority of filled and polymer patterns in terms of dimensional accuracy, pattern strength, surface and flow properties over unfilled wax is also discussed. The present use of 3D patterns following their versatility in the manufacturing sector to revolutionize the investment casting process is also emphasized. Various studies on wax characterization such as physical (surface and dimensions), thermal (thermogravimetric analysis and differential scanning calorimetry), mechanical (thermomechanical analysis, tensile stress testing, dynamic mechanical analysis) and rheological (viscosity and shearing properties) are also discussed.

Thermal and Mechanical Characterization of Jute-Biopol Nanophased Green Composites

2011 ◽  
Vol 1312 ◽  
Author(s):  
Mohammad K Hossain ◽  
Mohammad W Dewan ◽  
Mahesh Hosur ◽  
Shaik Jeelani
Keyword(s):  
Thermal Performance ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Jute Fiber ◽  
Degree Of Crystallinity ◽  
Fiber Reinforced ◽  
Molding Process ◽  
Scanning Calorimetry ◽  
Solution Intercalation ◽  
Jute Fibers

ABSTRACTSurface modification of jute fibers was accomplished by performing chemical treatments including detergent washing, dewaxing, alkali, and acetic acid treatment. Morphology of modified surfaces examined using scanning electron microscopy (SEM) revealed improved surfaces for better adhesion with matrix. Better thermal performance of treated fibers was found from thermogravimetric analysis (TGA). Enhanced tensile properties of treated fibers were obtained from tensile tests. Using solution intercalation technique and magnetic stirring, 2%, 3%, and 4% by weight Montmorillonite K10 nanoclay were dispersed into a biodegradable polymer, Biopol. Thermal performance of nanoclay infused Biopol characterized using dynamic scanning calorimetry (DSC) showed improved degree of crystallinity by 7%. Jute fiber reinforced Biopol biocomposites with and without nanoclay were manufactured using treated and untreated jute fibers by compression molding process. Thermal and mechanical responses of treated fiber reinforced Biopol composites (TJBC) without nanoclay evaluated using dynamic mechanical analysis (DMA) and flexure tests showed 9% and 12% increase in storage modulus and flexure strength, respectively, compared to untreated jute fiber reinforced composites (UTJBC). The respective values were 100% and 35% for 4% nanoclay infused TJBC compared to UTJBC without nanoclay.

Effect of Silane Treated and Untreated Talc on the Properties of Thermoplastic Polyurethane/Polypropylene Blends

2013 ◽  
Vol 849 ◽  
pp. 121-126 ◽  
Author(s):  
Emi Govorčin Bajsić ◽  
Filipan Veljko ◽  
Vesna Ocelić Bulatović
Keyword(s):  
Storage Modulus ◽  
Thermoplastic Polyurethane ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Mechanical And Thermal Properties ◽  
Scanning Calorimetry ◽  
Twin Screw ◽  
Mechanical Tensile ◽  
Polypropylene Blends ◽  
Pp Blends

The effect of the silane treated talc on the mechanical and thermal properties of talc filled thermoplastic polyurethane/polypropylene blends (TPU/PP blends) was investigated. Thermoplastic polyurethane and polypropylene are partially miscible due to the lack of interfacial interaction between the nonpolar crystalline PP and polar TPU. Blends of TPU and PP with silane treated and untreated-talc were prepared using melt blending in a laboratory twin-screw extruder. Organosilane (3-glycidoxypropyl-trimetoxy silane coupling agent) was used to treat talc in order to improve the affinity between the filler and the TPU/PP blends. Dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC) and mechanical (tensile test) measurements were used to characterize the talc filled and silane treated talc filled composites and TPU/PP/talc blends. The addition of silane treated and untreated talc in TPU/PP blends improved miscibility in all investigated TPU/PP/talc blends. The silane treatment increases the storage modulus in all investigated TPU/PP/talc blends in comparison with that of the untreated TPU/PP/talc blends. The obtained DSC results show that the addition of silane treated talc increases the degree of crystallinity (χc) of TPU/PP/talc blends because of the improved adhesion between the polymer and the treated talc. Addition of silane treated talc improved the mechanical properties as compared to TPU/PP/talc blends without chemical modification of talc. The results of strength correlate to the values of the storage modulus and crystallinity of the investigated TPU/PP/talc blends.

Sign in / Sign up

Export Citation Format

Share Document