Heat Deflection Temperature (heat + deflection_temperature)

Distribution by Scientific Domains


Selected Abstracts


Comparison of the effects of polyethylenimine and maleated polypropylene coupling agents on the properties of cellulose-reinforced polypropylene composites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008
C. González-Sánchez
Abstract The desire to improve the properties of cellulose-reinforced composites while producing them by methods as similar as possible to those used on an industrial scale is one of the driving forces in this field of research. In this work, extensive research for determining the mechanical, thermal, rheological, and physical properties of novel cellulose-reinforced polypropylene composites containing a polyethylenimine (PEI) coupling agent was conducted. A comparison of their properties with those of reference composites without any coupling agent or containing a maleated polypropylene (MAPP) coupling agent was also carried out. The presence of the PEI coupling agent mainly gave rise to a substantial increase in the tensile and flexural strengths and elongations as well as the impact strength, heat deflection temperature (HDT), melt volume flow index, and water absorption of PEI-containing composites in comparison with composites without any coupling agent added. However, the increases achieved in the tensile and flexural composite strengths and HDT were lower than those achieved with the MAPP coupling agent mainly for composites containing 50 wt % cellulose fibers. On the other hand, PEI-containing composites exhibited, in most cases, larger elongations and energies required to break in tensile tests as well as larger impact strengths, melt volume flow indices, and water absorption percentages than MAPP-containing composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]


Mechanical and thermal properties of polypropylene/sugarcane Bagasse composites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007
B. Ramaraj
Abstract To determine the possibility of using sugarcane bagasse (SCB) waste as reinforcing filler in the thermoplastic polymer matrix, SCB-reinforced polypropylene (PP) composites were prepared. The PP and SCB composites were prepared by the extrusion of PP resin with 5, 10, 15, and 20 wt % of SCB filler in a corotating twin screw extruder. The extruded strands were cut into pellets and injection molded to make test specimens. These specimens were tested for physicomechanical properties such as tensile, flexural, Izod, and Charpy impact strengths, density, water absorption, and thermal characteristics, namely, heat deflection temperature (HDT), melt flow index, and thermogravimetric analysis. It was found that the flexural strength increased from 23.66 to 26.84 MPa, Izod impact strength increased from 10.499 to 13.23 Kg cm/cm, Charpy impact strength increased from 10.096 to 13.98 Kg cm/cm, and HDT increased from 45.5 to 66.5°C, with increase in filler loading from 5 to 20% in the PP matrix. However, the tensile strength and elongation decreased from 32.22 to 27.21 MPa and 164.4 to 11.20% respectively. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3827,3832, 2007 [source]


Simultaneously improving the toughness, flexural modulus and thermal performance of isotactic polypropylene by ,-, crystalline transition and inorganic whisker reinforcement

POLYMER ENGINEERING & SCIENCE, Issue 2 2010
Yewen Cao
Magnesium salt (M-HOS) whisker and ,-nucleating agent were introduced into polypropylene and their effects on the crystalline structures, morphologies, mechanical properties, and thermal resistance of polypropylene (PP) were investigated. The results of wide angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), and polar optical microscopy (POM) examinations suggested that the presence of the whisker did not cause any negative effect on the occurrence of ,-modification, and ,-phase became absolutely dominant form in ,-nucleated samples. The mechanical and thermal properties tests demonstrated that there is an excellent synergy between the ,-nucleating agent and the whisker. For PP composite containing 0.1 wt% of the ,-nucleating agent and 10 wt% of the whiskers, the Izod notched impact strength, elongation at break, flexural modulus, and heat deflection temperature were increased by 108, 194, 31, and 40%, respectively, compared with those of neat PP. By combining the toughening effect of ,,, transition with the reinforcing effect of the whisker, simultaneous improvement in toughness, flexural modulus, and thermal performance of PP was successfully achieved. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers [source]


Studies on thermal and morphological properties of 1,1-bis(3-methyl-4-cyanatophenyl)cyclohexane-epoxy-bismaleimide matrices

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 8 2003
K. Dinakaran
Abstract A new cyanate ester monomer, 1,1-bis(3-methyl-4-cyanatophenyl)cyclohexane has been synthesized and characterized. Epoxy modified with 4, 8 and 12% (by weight) of cyanate ester were made using epoxy resin and 1,1-bis(3-methyl-4-cyanatophenyl)cyclohexane and cured by using diaminodiphenylmethane. The cyanate ester modified epoxy matrix systems were further modified with 4, 8 and 12% (by weight) of bismaleimide (N,N,-bismaleimido-4,4,-diphenylmethane). The formation of oxazolidinone and isocyanurate during cure reaction of epoxy and cyanate ester blend was confirmed by IR spectral studies. Bismaleimide-cyanate ester-epoxy matrices were characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and heat deflection temperature (HDT) analysis. Thermal studies indicate that the introduction of cyanate ester into epoxy resin improves the thermal degradation studies at the expense of glass transition temperature. Whereas the incorporation of bismaleimide into epoxy resin enhances the thermal properties according to its percentage content. However, the introduction of both cyanate ester and bismaleimide influences the thermal properties according to their percentage content. DSC thermogram of cyanate ester modified epoxy and bismaleimide modified epoxy show unimodel reaction exotherms. The thermal degradation temperature and heat distortion temperature of the cured bismaleimide modified epoxy and cyanate ester-epoxy systems increased with increasing bismaleimide content. The morphology of the bismaleimide modified epoxy and cyanate ester-epoxy systems were also studied by scanning electron microscopy. Copyright © 2003 John Wiley & Sons, Ltd. [source]


Recycled PCB flour reinforced linear low-density polyethylene composites enhanced by water cross-linking reaction

ASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 2 2009
Chen-Feng Kuan
Abstract Recycled printed circuit board (PCB) flour reinforced linear low-density polyethylene (LLDPE) composites were prepared successfully. Water cross-linking technique was adopted to improve the physical characteristics of the composites. Composites were compounded using a twin-screw extruder and treated with a coupling agent (vinyltrimethoxysilane, VTMOS) and a compatibilizer (polyolefin elastomer grafted with melaic acid, POE-g-MA). They were then moisture-cross-linked in hot water. The composite that was cross-linked in water exhibited better mechanical properties than the noncross-linked composite because of strong chemical bonding between the filler and the polyolefin matrix. When the PCB flour content reaches 60 wt% following 4 h of water cross-linking, the tensile strength and the flexural strength are increased by 18.8% (12.8,15.2 MPa) and 13.2% (21.9,24.8 MPa) respectively. Scanning electron microscopy (SEM) images of the fracture surfaces of water cross-linked composites indicated that good interfacial strength existed between the filler and the polyolefin matrix. Thermal analyses of water cross-linked composites indicated that the thermal degradation temperature and the heat deflection temperature (HDT) of the composite increased with the increasing of water cross-linking time. The HDT of the composite rose from 55.8 to 83 °C. Copyright © 2008 Curtin University of Technology and John Wiley & Sons, Ltd. [source]