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Macromolecular Chains (macromolecular + chain)

Distribution by Scientific Domains

Polymers and Materials Science	88%

Selected Abstracts

Synthesis and crystallization behavior of acetal copolymer/silica nanocomposite by in situ cationic ring-opening copolymerization of trioxane and 1,3-dioxolane

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008
Lanhui Sun
Abstract The acetal copolymer/silica nanocomposite was prepared by in situ bulk cationic copolymerization of trioxane and 1,3-dioxolane in the presence of nanosilica. The crystallization behavior of acetal copolymer/silica nanocomposite was studied by AFM, DSC, XRD, and CPOM, and the macromolecular structure of acetal copolymer/silica nanocomposite was characterized by FTIR and 1H-NMR. The 1H-NMR results showed that the macromolecular chain of acetal copolymer had more than two consecutive 1,3-dioxolane units in an oxymethylene main chain, while that of acetal copolymer/silica nanocomposite had only one 1,3-dioxolane unit in an oxymethylene main chain. There existed interaction between the macromolecular chains and nanoparticles (such as hydrogen bonds and coordination). On one hand, nanoparticles acted as nucleation center, which accelerated the crystallization rate but reduced the crystallinity. The spherulite sizes also decreased with addition of nanoparticles attributed to the nucleation effect. On the other hand, the presence of nanoparticles interrupted the spherical symmetry of the crystallite. In conclusion, the high surface energy and small scale of nanoparticles have a prominent impact on the polymerization mechanism and crystallization behavior of nanocomposite. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

Coil-Globule Collapse in Flexible Macromolecules

MACROMOLECULAR THEORY AND SIMULATIONS, Issue 9 2003
Bahattin M. Baysal
Abstract The transition of a solvated flexible macromolecular chain from random coil behavior in the , -state to a globular compact form in the collapsed state has been the subject of extensive theoretical and experimental studies. Most of the coil-globule transition studies of macromolecules have concentrated on the prototypical polystyrene-cyclohexane system. However, chain contractions reported in this system have been around 75% of those in the unperturbed , -state. This relatively small decrease in size does not satisfy the criterion for a densely packed, collapsed globule. Experimentally, the collapse from a coil to a true compact globular state has now been established for two flexible macromolecules: poly(N -isopropylacrylamide) in water and poly(methyl methacrylate) in various solvents. In this contribution, we review recent theoretical studies covering phenomenological and Langevin models as well as computer simulations. In addition, we outline recent experimental studies of the coil-globule transition of various flexible polymers, copolymers, and polyelectrolytes. Expansion factor, ,, versus temperature for NaPSS in 4.17 M aqueous NaCl solution. (,): NaPSS-1, (,): NaPSS-2. [source]

Heterocyclic polyimides containing siloxane groups in the main chain

POLYMER INTERNATIONAL, Issue 9 2009
Mariana-Dana Damaceanu
Abstract BACKGROUND: Among the polymers widely studied for applications in advanced techniques, aromatic polyimides have received considerable attention due to their outstanding thermal stability associated with good electrical and mechanical properties. However, these polymers are usually difficult to process, being insoluble and without a glass transition. To improve the processing characteristics of polyimides, modification of their structure is often achieved by the introduction of flexible linkages in the macromolecular chain or various substituents on the aromatic rings. RESULTS: A series of polyimides and intermediate polyamidic acids were synthesized from aromatic oxadiazole-diamines and a dianhydride containing a siloxane bridge (R2SiOSiR2). These polymers exhibit good solubility in certain organic solvents and can be cast into thin and very thin films from their solutions. They exhibit high thermal stability with decomposition being above 440 °C and relatively low glass transition temperatures in the range 160,190 °C. These polymers show strong photoluminescence in the blue spectral region. CONCLUSION: The introduction of oxadiazole rings together with siloxane groups into the chains of aromatic polyimides gives highly thermostable polymers with remarkable solubility and film-forming ability and that emit blue light, being attractive for applications in micro- and nanoelectronics and other related advanced fields. Copyright © 2009 Society of Chemical Industry [source]

Study on bulk polymerization of methyl methacrylate initiated by low intensity ultrasonic irradiation

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010
Sude Ma
Abstract Methyl methacrylate (MMA) was polymerized in bulk solutions using low intensity ultrasonic radiation of 0.25 W/cm2. The polymerization occurred after 1 h of irradiation time was applied. The polymerization rate was greatly accelerated either by increasing the amount of poly (methyl methacrylate) (PMMA) granular added into the system or by elongating the irradiation time. However, it was found that the reaction rate increased with the decreasing of the ultrasonic frequencies when the exposure time of the polymerization under the irradiation was less than 3 h. Experimental results verified that the polymerization was initiated by free radicals, which were mainly generated from the degradation of PMMA macromolecular chains, the friction between the polymer macromolecular chains and the solvent monomer. These findings were obviously different from those obtained when high intensity ultrasonic irradiation was used. The polymers fabricated in this study by using ultrasound irradiation have a narrower molecular weight distribution compared to those obtained from the polymerizations induced by the conventional initiators. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Mechanical and functional properties of composites based on graphite and carboxylated acrylonitrile butadiene rubber

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010
Jian Yang
Abstract In this study, carboxylated acrylonitrile butadiene rubber (xNBR)/expanded graphite (EG) nanocomposites were prepared with a latex compounding technique by ultrasonic stirring. The dispersion of EG in the xNBR matrix was investigated with transmission electron microscopy, scanning electron microscopy, and X-ray diffraction analysis. EG could be exfoliated into lots of nanosheets dispersing in the xNBR matrix. More EG loading resulted in the presence of a few incompletely exfoliated agglomerates. The mechanical properties (hardness, tensile modulus, and tensile strength) of the xNBR/EG composites were determined. Dynamic mechanical thermal analysis was also performed, and it showed that the nanosheets of EG somewhat immobilized the motion of rubber macromolecular chains and led to the shifting and broadening of the tan , peak toward higher temperatures. Many other functional properties of EG-filled xNBR composites were studied, and it was established that the composites had excellent electrical conductivity as well as gas-barrier and wear properties. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Synthesis and crystallization behavior of acetal copolymer/silica nanocomposite by in situ cationic ring-opening copolymerization of trioxane and 1,3-dioxolane

Copolymers based on poly(butylene terephthalate) and polycaprolactone- block -polydimethylsiloxane- block -polycaprolactone

POLYMER INTERNATIONAL, Issue 6 2010
Vesna V Anti
Abstract A series of novel thermoplastic elastomers, based on poly(butylene terephthalate) (PBT) and polycaprolactone- block -polydimethylsiloxane- block -polycaprolactone (PCL-PDMS-PCL), with various mass fractions, were synthesized through melt polycondensation. In the synthesis of the poly(ester-siloxane)s, the PCL blocks served as a compatibilizer for the non-polar PDMS blocks and the polar comonomers dimethyl terephthalate and 1,4-butanediol. The introduction of PCL-PDMS-PCL soft segments resulted in an improvement of the miscibility of the reaction mixture and therefore in higher molecular weight polymers. The content of hard PBT segments in the polymer chains was varied from 10 to 80 mass%. The degree of crystallinity of the poly(ester-siloxane)s was determined using differential scanning calorimetry and wide-angle X-ray scattering. The introduction of PCL-PDMS-PCL soft segments into the polymer main chains reduced the crystallinity of the hard segments and altered related properties such as melting temperature and storage modulus, and also modified the surface properties. The thermal stability of the poly(ester-siloxane)s was higher than that of the PBT homopolymer. The inclusion of the siloxane prepolymer with terminal PCL into the macromolecular chains increased the molecular weight of the copolymers, the homogeneity of the samples in terms of composition and structure and the thermal stability. It also resulted in mechanical properties which could be tailored. Copyright © 2010 Society of Chemical Industry [source]

Structure and properties of star-shaped solution-polymerized styrene-butadiene rubber and its co-coagulated rubber filled with silica/carbon black-I: morphological structure and mechanical properties

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11 2009
Xiao Liu
Abstract The morphological structure and mechanical properties of the star-shaped solution-polymerized styrene-butadiene rubber (SSBR) and organically modified nanosilica powder/star-shaped SSBR co-coagulated rubber (N-SSBR) both filled with silica/carbon black (CB) were studied. The results showed that, compared with SSBR, silica powder could be mixed into N-SSBR much more rapidly, and N-SSBR/SiO2 nanocomposite had better filler-dispersion and processability. N-SSBR/SiO2/CB vulcanizates displayed higher glass-transition temperature and lower peak value of internal friction loss than SSBR/SiO2/CB vulcanizates. In the N-SSBR/SiO2/CB vulcanizates, filler was dispersed in nano-scale resulting in good mechanical properties. Composites filled with silica/CB doped filler exhibited more excellent mechanical properties than those filled with a single filler because of the better filler-dispersion and stronger interfacial interaction with macromolecular chains. N-SSBR/SiO2/CB vulcanizates exhibited preferable performance in abrasion resistance and higher bound rubber content as the blending ratio of silica to CB was 20:30. Copyright © 2008 John Wiley & Sons, Ltd. [source]

Rapid and Effective Adsorption of Lead Ions on Fine Poly(phenylenediamine) Microparticles

CHEMISTRY - A EUROPEAN JOURNAL, Issue 16 2006
Mei-Rong Huang Prof.
Abstract Fine microparticles of poly(p -phenylenediamine) (PpPD) and poly(m -phenylenediamine) (PmPD) were directly synthesized by a facile oxidative precipitation polymerization and their strong ability to adsorb lead ions from aqueous solution was examined. It was found that the degree of adsorption of the lead ions depends on the pH, concentration, and temperature of the lead ion solution, as well as the contact time and microparticle dose. The adsorption data fit the Langmuir isotherm and the process obeyed pseudo-second-order kinetics. According to the Langmuir equation, the maximum adsorption capacities of lead ions onto PpPD and PmPD microparticles at 30,°C are 253.2 and 242.7 mg,g,1, respectively. The highest adsorptivity of lead ions is up to 99.8,%. The adsorption is very rapid with a loading half-time of only 2 min as well as initial adsorption rates of 95.24 and 83.06 mg,g,1 min,1 on PpPD and PmPD particles, respectively. A series of batch experiment results showed that the PpPD microparticles possess an even stronger capability to adsorb lead ions than the PmPD microparticles, but the PmPD microparticles, with a more-quinoid-like structure, show a stronger dependence of lead-ion adsorption on the pH and temperature of the lead-ion solution. A possible adsorption mechanism through complexation between Pb2+ ions and N groups on the macromolecular chains has been proposed. The powerful lead-ion adsorption on the microparticles makes them promising adsorbents for wastewater cleanup. [source]