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Rubbery Polymer (rubbery + polymer)

Distribution by Scientific Domains
Polymers and Materials Science100%

Selected Abstracts

Polymerization of linseed oil with phenolic resins

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010
Gökhan Çayl
Abstract In this study, linseed oil was directly polymerized with different oil soluble resoles. p- Ethyl (PEP), p-tertiary butyl (PTB), p-tertiary octyl (PTO), and p- phenyl (PPP) phenols were separately reacted with formaldehyde to give linseed oil soluble resoles. These were then reacted with linseed oil to give transparent rubbery polymers. A model reaction was performed with methyl oleate and PTB phenol resole to clarify the reaction mechanism. Reaction products were characterized with 1H-NMR and IR techniques. Spectral examination of the model reaction showed that polymerization reaction proceeded via ene reaction of the quinone methide formed at the end group of the resole with the allylic positions of the fatty ester. Rubbery polymers were obtained with linseed oil using 10 to 40% of the different resoles. Hard, load bearing and tough materials were obtained at 40% phenolic resin loading. Mechanical properties of the materials were characterized by dynamic mechanical analyzer (DMA) and stress,strain tests. The best mechanical and thermal properties were obtained with PEP resole which showed a storage modulus of 350 MPa and a tan , peak at 65°C. Storage moduli of 275, 250, and 30 were obtained for PPP, PTB, and PTO resoles-linseed oil polymers, respectively. At the same phenolic resin loading, elongation at break and swelling ratios in CH2Cl2 increased with the longer alkyl substitution on the resole resins. The highest thermal stability was observed by PEP resole,linseed oil polymer which has a 5% weight loss temperature of 340°C as determined by TGA. The lowest thermal stability was observed for PTB resole-linseed oil polymer at 220°C. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Actuation in Crosslinked Polymers via Photoinduced Stress Relaxation,

ADVANCED MATERIALS, Issue 16 2006
F. Scott
Photoinduced polymer actuation by relieving stress unevenly through the thickness of a chemically crosslinked, rubbery polymer upon light exposure is demonstrated (see figure). The sensitivity of this method to light is greater than previously developed photoinduced actuation techniques, as the recurring chain-transfer reactions amplify the effects of each absorbed photon and subsequently generated radical on the stress-relief and actuation processes. [source]

Synergetic behavior of low Tg polybutadiene polymers and polysiloxanes as components for glass fiber sizing in composite materials

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010
Katherine M. Danner
Abstract The effect of low Tg polybutadiene (PBD) rubbery polymer as a part of polysiloxane/PBD E-glass fibers sizing on mechanical properties of a corresponding epoxy composite material has been evaluated by the punch shear test technique. The results show that the use of hydroxyl terminated PBD led to significant increase in interface shear strength, energy absorption, as well as dynamic modulus and Tg in a corresponding composite material. The sizing composition and fiber morphology were characterized by FTIR spectroscopy and AFM microscopy, respectively. Possible rational for such sizing composition/material property relationship is discussed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Polymerization of linseed oil with phenolic resins

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010
Gökhan Çayl
Abstract In this study, linseed oil was directly polymerized with different oil soluble resoles. p- Ethyl (PEP), p-tertiary butyl (PTB), p-tertiary octyl (PTO), and p- phenyl (PPP) phenols were separately reacted with formaldehyde to give linseed oil soluble resoles. These were then reacted with linseed oil to give transparent rubbery polymers. A model reaction was performed with methyl oleate and PTB phenol resole to clarify the reaction mechanism. Reaction products were characterized with 1H-NMR and IR techniques. Spectral examination of the model reaction showed that polymerization reaction proceeded via ene reaction of the quinone methide formed at the end group of the resole with the allylic positions of the fatty ester. Rubbery polymers were obtained with linseed oil using 10 to 40% of the different resoles. Hard, load bearing and tough materials were obtained at 40% phenolic resin loading. Mechanical properties of the materials were characterized by dynamic mechanical analyzer (DMA) and stress,strain tests. The best mechanical and thermal properties were obtained with PEP resole which showed a storage modulus of 350 MPa and a tan , peak at 65°C. Storage moduli of 275, 250, and 30 were obtained for PPP, PTB, and PTO resoles-linseed oil polymers, respectively. At the same phenolic resin loading, elongation at break and swelling ratios in CH2Cl2 increased with the longer alkyl substitution on the resole resins. The highest thermal stability was observed by PEP resole,linseed oil polymer which has a 5% weight loss temperature of 340°C as determined by TGA. The lowest thermal stability was observed for PTB resole-linseed oil polymer at 220°C. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Sorption behavior in polymers above Tg: Relations between mechanical properties and swelling in limonene

POLYMER ENGINEERING & SCIENCE, Issue 9 2005
J.E. Ritums
The sorption behavior of two highly swelling "rubbery" polymers, natural rubber and polyethylene, has been studied. The polymers are in many aspects very different. Yet, when the solute mass uptake, in this case limonene, is plotted as a function of the square root of time, both polymers show similar "sigmoidal"-types of curves. This triggered the research to determine what mechanisms were responsible for the observed similarities and if the degree in sigmoidal behavior and swelling anisotropy could be easily assessed explicitly by any mechanical parameter. It was found that their degrees of swelling anisotropy, described by a solute-surface-concentration relaxation time, could be explained by their relative bulk moduli. It was assumed that the ratio in bulk modulus at zero pressure, determined from compression measurements, could represent the ratio in expansion bulk modulus during swelling. However, the prediction in swelling anisotropy during sorption using the ratio in bulk modulus was slightly less successful when the swelling anisotropy was quantified as the relative ratio of sheet thickness to cross-sectional area side length. It should be noted that the ratio in uniaxial tensile modulus between polyethylene and natural rubber was several orders of magnitude higher than their ratio in swelling anisotropy. The natural rubber sheet became saddle-shaped during limonene sorption and collapsed into a flat shape when the saturation concentration was approached. During desorption, the sheet went from flat to cup-shaped and then flat again at the end of desorption. The saddle and cup shapes occurred in both square and round sheets. These shapes are believed to be a consequence of buckling and deformation due to instabilities in the stress state of the sheet. This was, in turn, explained by the normally existing local variation in cross-link density. POLYM. ENG. SCI., 45:1194,1202, 2005. © 2005 Society of Plastics Engineers [source]