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Decomposition Temperature (decomposition + temperature)
Kinds of Decomposition Temperature Selected AbstractsPrediction of Decomposition Temperature for Lanthanide Complexes Involving Cyclopentadienyl and Benzohydroxamic Acid Ligand by ANNsCHINESE JOURNAL OF CHEMISTRY, Issue 10 2002Yi-Min Sun Abstract The decomposition temperatures of the lanthanide organic complexes (,5 -C5H5)2 Ln(C6H5CONHO) involving cyclopentadienyl and benzohydroxamic acid ligands were calculated and predicted by the model based on ANNs (artificial neural networks) method. The comparison was carried out between results from ANNs method and traditional regression method. It is proved that ANNs could be used more efficiently for the prediction of decomposition temperature of lanthanide organic complexes. [source] Influence of the starting powders on the synthesis of nickel ferriteCRYSTAL RESEARCH AND TECHNOLOGY, Issue 8 2006F. Kenfack Abstract The thermal decomposition of freeze-dried nickel(II)-iron(III) formate was investigated by means of DTA, TG, mass spectrometry and X-ray powder diffractometry. For the preparation of homogeneous freeze-dried nickel(II)-iron(III) formate precursors, a rigorous control of nickel ion concentration in the precursor solution was required. The decomposition of the reactive nickel(II)-iron(III) formate does not only reflect aspects of single formates, but also an interaction between components which lowers the decomposition temperature. Crystalline nickel ferrite powders were obtained at 600-800°C. This temperature is quite lower than 1100°C employed for the ceramic method. In the presence of air, the regeneration of nickel ferrite from the taenite phase (,Ni,Fe) is accomplished at 800°C. This temperature is also 300°C below the temperature employed when the mixtures NiO:,-Fe2O3 or Ni:2Fe are the starting powders. The main reason for the high reactivity of the freeze-dried formates and the taenite alloy is the large homogeneity of these precursors. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Thermal Decomposition Reactions as a Tool for the Synthesis of New Thermodynamic Metastable Modifications: Synthesis, Structures, and Properties of (Formato)nickel(II) Coordination Polymers Based on 4,4,-BipyridineEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 12 2010Jan Boeckmann Abstract The reaction of nickel formate with 4,4,-bipyridine (bipy) in aqueous solution at room temperature leads to the formation of the hydrated compound [Ni(HCO2)2(H2O)(bipy)·4H2O]n (1) reported recently. On heating, compound 1 decomposes into the new anhydrous compound of composition [Ni(HCO2)2(bipy)]n (2II), which decomposes on further heating. Interestingly, if the anhydrous compound is prepared from solution, a new modification 2I is obtained. Investigations on the stability of both forms show that modification 2I presents the thermodynamically most stable form between room and decomposition temperature, whereas modification 2II, which can only be prepared by thermal decomposition, is metastable. In the crystal structure of 2I, the Ni2+ cations are coordinated by four ,2 - anti,anti bridging formato anions and two bridging ,2 -bipy ligands in a slightly distorted octahedralgeometry. The formato anions bridge the metal cations in zigzag chains, which are further connected by ,2 - anti,anti formato anions and bipy ligands to give a three-dimensional coordination network. IR spectroscopic investigations on the metastable form 2II also indicate that all formato anions act as bridging ligands. Magnetic measurements of the hydrated and anhydrous compounds reveal different behavior with a ferromagnetic ordering for compound 2I and an antiferromagnetic ordering for compound 1. For form 2II, only Curie,Weiss paramagnetism was found. [source] Rotational foam molding of polypropylene with control of melt strengthADVANCES IN POLYMER TECHNOLOGY, Issue 4 2003Remon Pop-Iliev Abstract Polypropylene (PP) has not been used extensively in rotational foam molding because it has been traditionally considered as nonfavorable for foaming applications because of its relatively weak melt strength and melt elasticity at elevated temperatures. However, because of the unique end-use properties of PP, PP foams have recently grown in importance. An experimental study was conducted to identify feasible processing strategies for producing PP foams with satisfactory morphologies in dry-blending-based rotational foam molding. The obtained results revealed that cell coalescence plays a key role in the production of PP foams in rotational foam molding. If it is efficiently suppressed, the cell morphology of the PP foams improves dramatically. To suppress cell coalescence, it would be necessary to preserve the melt strength of PP during processing. One way of doing this is maintaining the temperature of the PP melt as low as possible. This can be accomplished by either lowering the decomposition temperature of the chemical blowing agent by using an activator such as zinc oxide and/or reducing the temperature of the oven. © 2003 Wiley Periodicals, Inc. Adv Polym Techn 22: 280,296, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.10056 [source] Effect of boron-containing materials on the flammability and thermal degradation of polyamide 6 composites containing melamineJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Mehmet Do Abstract Three different boron-containing substances,zinc borate (ZnB), borophosphate (BPO4), and a boron- and silicon-containing oligomer (BSi),were used to improve the flame retardancy of melamine in a polyamide 6 (PA-6) matrix. The combustion and thermal degradation characteristics of PA-6 composites were investigated with the limiting oxygen index (LOI), the UL-94 standard, thermogravimetric analysis (TGA)/Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC). A slight increase was seen in the LOI values of a sample containing BSi (1 wt %). BPO4 at high loadings showed a V0 rating (indicating the best flame retardancy) and slightly lower LOI values in comparison with samples with only melamine. For ZnB and BSi, glassy film and char formation decreased the dripping rate and sublimation of melamine, and this led to low LOIs. According to the TGA,FTIR results, the addition of boron compounds did not change the decomposition product distribution of melamine and PA-6. The addition of boron compounds affected the flame retardancy by physical means. The TGA data showed that boron compounds and melamine reduced the decomposition temperature of PA-6. According to the DSC data, the inclusion of boron compounds increased the onset temperature of sublimation of melamine and also affected the flame retardancy negatively. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Preparation of novel polyindene/polyoxymethylene blends and investigation of their propertiesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010Tenzile Zilhan Cabuk Abstract In this study, the conducting homopolymer of indene was synthesized by a chemical polymerization method in a nonaqueous medium, and polyindene (PIn)/polyoxymethylene (POM) blends were prepared. The physical, chemical, thermal, and spectral properties of the synthesized homopolymer and their blends were investigated. The conductivities of PIn and the PIn/POM blends were measured with a four-probe technique. The conductivity of PIn was determined as 1.16 × 10,5 S/cm, whereas the conductivities of the PIn/POM blends were determined to be in the range 3.16 × 10,6 to 9.8 × 10,6 S/cm. From Gouy scale magnetic susceptibility measurements, we found that PIn and the PIn/POM blends had polaron natures. The amount of Fe (milligrams per gram) in the PIn and PIn/POM structures were determined by inductively coupled plasma,optic emission spectrometry. Fourier transform infrared spectra were taken to analyze the structural properties of PIn and the PIn/POM blends. The thermal properties of PIn and PIn/POM blends were investigated with thermogravimetric analysis and differential scanning calorimetry analyses, and we found that they showed adequate thermal stability. According to the initial decomposition temperature among the blends, the blend including 16% PIn had the highest decomposition temperature with 244°C. The morphological structures of the PIn, POM, and blends were clarified with scanning electron microscopy. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Effects of membrane thickness and heat treatment on the gas transport properties of membranes based on P84 polyimideJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Yi Shen Abstract P84 polyimide membranes with thicknesses ranging from 6 to 310 ,m were successfully fabricated by spin coating. The glass transition temperature of the P84 powder was found to be 315°C using differential scanning calorimetry, whereas its decomposition temperature was 536°C using thermogravimetric analysis. Scanning electron microscopy was used to examine the morphology of the membranes. The permeability of single gas (He, N2, O2, and CO2) and the ideal selectivity of gas pair (O2/N2, He/CO2, CO2/N2, and He/O2), as a function of membrane thickness, were determined. The results showed that the permeability of a single gas increased with increasing membrane thickness, whereas the selectivity of a given gas pair was nearly independent of the membrane thickness. The average selectivity of O2/N2, He/CO2, CO2/N2, and He/O2 were found to be 8.2, 10.0, 12.9, and 15.8, respectively. The effects of heat treatment on the membrane morphology and gas transport properties were investigated for three annealing temperatures, i.e., 80°C, 200°C, and 315°C. The membrane annealed at 315°C was cracked due to the stress sustained either during heating or cooling, thereby resulting in little or no selectivity. The permeabilities of P84-118 membrane (118 ,m thickness) annealed at 80°C were 16.2, 0.196, 1.20, and 2.01 Barrer for He, N2, O2, and CO2, respectively. The permeabilities of P84-118 membrane annealed at 200°C decreased by 9.75%, 47.96%, 25.83%, and 30.85% for He, N2, O2, and CO2, respectively, as compared with those at 80°C, whereas the ideal selectivities increased by 42.65%, 30.52%, 32.85%, and 21.63% for O2/N2, He/CO2, CO2/N2, and He/O2, respectively. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Morphology, mechanical properties, and thermal stability of poly(L -lactic acid)/poly(butylene succinate- co -adipate)/silicon dioxide compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2009Ruyin Wang Abstract Poly(butylene succinate- co -adipate) (PBSA) and two types of SiO2 (hydrophilic or hydrophobic) were used to modify poly(L -lactic acid) (PLLA). The mechanical properties, rheological and thermal behavior, phase morphology, and thermal stability of PLLA/PBSA/SiO2 composites were investigated. The impact strength, flexural strength, and modulus of PLLA/PBSA blends increased after the addition of hydrophobic SiO2 without decreasing the elongation at break, and the elongation at break monotonically decreased with increasing hydrophilic SiO2 content. The melt elasticity and viscosity of the PLLA/PBSA blend increased with the addition of SiO2. The hydrophilic SiO2 was encapsulated by the dispersed PBSA phase in the composites, which led to the formation of a core,shell structure, whereas the hydrophobic SiO2 was more uniformly dispersed and mainly located in the PLLA matrix, which was desirable for the optimum reinforcement of the PLLA/PBSA blend. The thermogravimetric analysis results show that the addition of the two types of SiO2 increased the initial decomposition temperature and activation energy and consequently retarded the thermal degradation of PLLA/PBSA. The retardation of degradation was prominent with the addition of hydrophobic SiO2. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Hydrogenated natural rubber blends: Aspect on thermal stability and oxidative behaviorJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009N. Hinchiranan Abstract Hydrogenated natural rubber (HNR) prepared from natural rubber (NR) is a new sustainable elastomer with excellent thermal properties. This study reports on the effect of vulcanization system and blend ratio on the thermal and oxidative resistance of HNR/NR vulcanizates. The various HNR/NR ratios vulcanized by peroxide and sulfur donor system exhibited the highest retention of tensile strength after thermal aging due to the formation of zinc-dimethyldithiocarbamate (ZDMDC) which is an efficient antioxidant. The results from thermogravimetric analysis (TGA) indicated that the saturated structure of HNR had higher decomposition temperature and activation energy to enhance the thermal stability of HNR/NR vulcanizates. The initial and maximum decomposition temperatures of NR and HNR phases in vulcanizates were not affected by rubber blend ratio. This suggests that the decomposition pattern of HNR has no influence on another constituent. The increase in HNR content in the blends could retard the ozonolysis resulting in the surface cracking attacked by ozone. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Synthesis and characterization of polypyrrole rod doped with p -toluenesulfonic acid via micelle formationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Duk Ki Kim Abstract Rod-type polypyrrole (PPY) doped with p -toluenesulfonic acid (TSA) was synthesized by chemical oxidative polymerization via a self-assembly process. The shape of the PPY particles is mainly determined by the ratio of TSA/pyrrole (PY) and feed rate of the oxidant. Particle of different shapes (rod, grain, and partially rod) exhibit differences in morphology, electrical properties, dispersity, and thermal properties. Wide-angle X-ray diffraction patterning analysis was used to investigate the mechanism of rod formation. The effect of the TSA concentration on the PPY structure was investigated using Fourier transform infrared spectroscopy. The PPY rods doped with TSA exhibited better electrical conductivity than granular PPY doped with TSA, and their dispersity and thermal stability were also higher. Self-orientation of PPY in the micelles of TSA and high crystallinity of the rod particles led to improved thermal stability. Hence, the decomposition temperature of the polymer chain was considerably increased. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Novel adamantane-containing epoxy resinJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007Xiaoming Su Abstract A novel adamantane-containing epoxy resin diglycidyl ether of bisphenol-adamantane (DGEBAda) was successfully synthesized from 1,3-bis(4-hydroxyphenyl)adamantane by a one-step method. The proposed structure of the epoxy resin was confirmed with Fourier transform infrared, 1H-NMR, gel permeation chromatography, and epoxy equivalent weight titration. The synthesized adamantane-containing epoxy resin was cured with 4,4,-diaminodiphenyl sulfone (DDS) and dicyandiamide (DICY). The thermal properties of the DDS-cured epoxy were investigated with differential scanning calorimetry and thermogravimetric analysis (TGA). The dielectric properties of the DICY-cured epoxy were determined from its dielectric spectrum. The obtained results were compared with those of commercially available diglycidyl ether of bisphenol A (DGEBA), a tetramethyl biphenol (TMBP)/epoxy system, and some other associated epoxy resins. According to the measured values, the glass-transition temperature of the DGEBAda/DDS system (223°C) was higher than that of the DGEBA/DDS system and close to that of the TMBP/DDS system. TGA results showed that the DGEBAda/DDS system had a higher char yield (25.02%) and integral procedure decomposition temperature (850.7°C); however, the 5 wt % degradation temperature was lower than that of DDS-cured DGEBA and TMBP. Moreover, DGEBAda/DDS had reduced moisture absorption and lower dielectric properties. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Synthesis and characterization of copolythiopheneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Jie He Abstract Copolythiophenes (Co-PTs), poly(3-hexylthiophene- co -3-thiophene carboxylic acid) (P3HT-TCa), poly(3-hexyloxylthiophene- co -3-thiophene carboxylic acid) (P3HOT-TCa), and poly(3-phenylthiophene- co -3-thiophene carboxylic acid) (P3PhT-TCa), were synthesized by chemical oxidized polymerization to investigate the effect of copolymerization on the properties of polythiophenes (PTs). Gel permeation chromatography showed that the molecular weight (MW) of Co-PT was lower than that of homopolythiophene. Fourier transform infrared (FTIR) spectra indicated that the copolymerization was successful between the monomers. The ,max of Co-PTs gave a "blue shift" in ultraviolet-visible (UV-VIS) spectra. Photoluminescence (PL) spectra showed that the PL intensity of Co-PT became weaker than that of homopolythiophene and the disappearance of PL had been observed in P3HOT-TCa. The thermal stability of Co-PT was influenced by the carboxyl for its low decomposition temperature. Furthermore, the copolymerization between multi-wall carbon nanotube containing thiophene ring (MWNT-Th) and 3-hexyloxylthiphene could also take place successfully. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Synthesis of organic,inorganic hybrid polymeric nanocomposites for the hard coat applicationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Chuan Hsiao Shu Abstract An organic,inorganic hybrid polymeric nanocomposite has been synthesized for making UV-curable hard coats. This nanocomposite consists of nano-sized colloidal silica functionalized with vinyltriethoxysilane (VTES) and dendritic acrylic oligomers (DAO) which have been formed earlier via a reaction of ethylenediamine (EDA) with trimethylopropane triacrylate (TMPTA). Applied as a hard coat on top of a polyethylene terephthalate (PET) film, this nanocomposite has a short UV-cure time and the cured coat has an enhanced thermal decomposition temperature (Td), 89,90% transparency, increased hardness up to 3H, better adhesion up to 4B, and a flat surface with a root mean square roughness of 2,4 nm. The preparation as well as the characterization of the constituting species and the final hybrid are described in detail. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3985,3993, 2007 [source] Fabrication, structures, and properties of acrylonitrile/methyl acrylate copolymers and copolymers containing microencapsulated phase change materialsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007Na Han Abstract The polyacrylonitrile-methyl acrylate (AN/MA mole ratio 100/0,70/30) copolymers and copolymers (AN/MA mole ratio 85/15) containing up to 40 wt % of microencapsulated n -octadecane (MicroPCMs) are synthesized in water. The MicroPCMs were incorporated at the step of polymerization. The effect of the MA mole ratio and MicroPCMs content on structures and properties of the copolymers were studied by using Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (1H NMR), scanning electronic microscope (SEM), differential scanning calorimetry (DSC), thermogravimetry analysis (TG), gel permeation chromatography (GPC), and X-ray diffraction (XRD). The feeding ratio agreed well with the composition of the AN/MA copolymers. The copolymers are synthesized in the presence of MicroPCMs. The melting point moves to lower temperature (206°C), while the decomposition temperature moves to higher temperature (309°C) with increasing of the MA mole ratio and microcapsules content. The number,average molecular weight of the copolymer is ,30,000. The crystallinity of the copolymer decreases with increasing of the MA mole ratio and microcapsules content. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2776,2781, 2007 [source] An engineering-purpose preparation strategy for ammonium-type ionic liquid with high purityAICHE JOURNAL, Issue 4 2010Xiaoqi Sun Abstract A new strategy for preparing ammonium-type ionic liquid (IL) by acid/base neutralization reaction was proposed. The method contributed to preparing hydroxide-based ammonium IL and resulting task specific ionic liquid (TSIL) with high purity using a low-costly and environment-friendly synthetic route. Halide contamination in the prepared ILs could be markedly decreased than those prepared by well-established anion metathesis method. Moreover, some novel TSILs composed of cations and anions with big steric hindrances could be prepared by this method. Physicochemical properties of the bifunctional TSILs, i.e., density, water content, decomposition temperature, and munal solubility, were also studied in this article. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Exothermic thermal reaction of dopamine with 3,5-dinitrobenzoic acidJOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 11 2003Yoshikatsu Ito Abstract Pyrolysis of the crystalline 1,:,1 molecular complex DA,dnba, which was prepared from cocrystallization of dopamine (DA) and 3,5-dinitrobenzoic acid (dnba), was studied. This cocrystal decomposed violently at the melting-point, leading to the formation of a black solid along with a tiny amount of 3-amino-5-nitrobenzoic acid (1). The pyrolysis reaction was followed by differential scanning calorimetry (DSC) and one large exothermic peak was observed at the decomposition temperature. In view of the DSC patterns for cocrystal DA,dnba and other compounds, it seems that both a catechol moiety and an amino group of DA in addition to a strong electron acceptor such as dnba are required for the appearance of the exothermic peak. On the basis of (a) elemental analysis of the black solid and (b) other pyrolysis experiments for cocrystals PA,dnba (PA: ,-phenylethylamine), BA,dnba (BA: benzylamine), DMDA,dnba (DMDA: O,O,-dimethyldopamine) and DHBA,dnba (DHBA: 3,4-dihydroxybenzylamine), it is assumed that the black solid was formed mainly through elimination of more than one molecule of water from one molecule of DA,dnba. Copyright © 2003 John Wiley & Sons, Ltd. [source] Living cationic polymerization of 2-adamantyl vinyl etherJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2008Tamotsu Hashimoto Abstract Living cationic polymerization of 2-adamantyl vinyl ether (2-vinyloxytricyclo[3.3.1.1]3,7decane; 2-AdVE) was achieved with the CH3CH(OiBu)OCOCH3/ethylaluminum sesquichloride/ethyl acetate [CH3CH(OiBu)OCOCH3/Et1.5AlCl1.5/CH3COOEt] initiating system in toluene at 0 °C. The number-average molecular weights (Mn's) of the obtained poly(2-AdVE)s increased in direct proportion to monomer conversion and produced the polymers with narrow molecular weight distributions (MWDs) (Mw/Mn = ,1.1). When a second monomer feed was added to the almost polymerized reaction mixture, the added monomer was completely consumed and the Mn's of the polymers showed a direct increase against conversion of the added monomer. Block and statistical copolymerization of 2-AdVE with n -butyl vinyl ether (CH2CHOCH2 CH2CH2CH3; NBVE) were possible via living process based on the same initiating system to give the corresponding copolymers with narrow MWDs. Grass transition temperature (Tg) and thermal decomposition temperature (Td) of the poly(2-AdVE) (e.g., Mn = 22,000, Mw/Mn = 1.17) were 178 and 323 °C, respectively. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1629,1637, 2008 [source] Stereoregular P(MMA)-clay nanocomposites by metallocene catalysts: In situ synthesis and stereocomplex formationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 13 2007Wesley R. Mariott Abstract This contribution reports the synthesis and characterization of stereochemically controlled, as well as crystalline stereocomplex, P(MMA)-clay nanocomposites using metallocene complexes and alane-intercalated clay activators. The ligand elimination and exchange reactions involving Lewis acids E(C6F5)3 (E = Al, B) and an organically modified montmorillonite clay were employed to synthesize the alane-intercalated clay activators. When combined with dimethyl metallocenes of various symmetries, these clay activators brought about efficient MMA polymerizations leading to in situ polymerized, stereochemically controlled P(MMA)-intercalated clay nanocomposites. The most noticeable thermal property enhancement observed for the clay nanocomposite P(MMA), when compared with the pristine P(MMA) having similar molecular weight and stereomicrostructure, has a considerable increase in Tg (,10 °C). Mixing of dilute THF solutions of two diastereomeric nanocomposites in a 1:2 isotactic to syndiotactic ratio, followed by reprecipitation or crystallization procedures, yielded unique double-stranded helical stereocomplex P(MMA)-clay nanocomposites with a predominantly exfoliated clay morphology. Remarkably, the resulting crystalline stereocomplex P(MMA) matrix is resistant to the boiling-THF extraction and its clay nanocomposites exhibit high Tm of 201 to 210 °C. Furthermore, the stereocomplex P(MMA)-clay nanocomposite shows a one-step, narrow decomposition temperature window and a single, high maximum rate decomposition temperature of 377 °C. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2581,2592, 2007 [source] Synthesis and properties of the polythiourethanes obtained by the cationic ring-opening polymerization of cyclic thiourethanesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 16 2006Daisuke Nagai Abstract The cationic ring-opening polymerization of a five-membered thiourethane [3-benzyl-1,3-oxazolidine-2-thione (BOT)] with boron trifluoride etherate afforded the corresponding polythiourethane with a narrow molecular weight distribution in an excellent yield. The molecular weight of the polymers could be controlled by the feed ratio of the monomer to the initiator. A kinetic study of the polymerization revealed that the polymerization rate of BOT (1.3 × 10,2 L mol,1 min,1) was two times larger than that of the six-membered thiourethane [3-benzyltetrahydro-1,3-oxazolidine-2-thione (BTOT); 6.8 × 10,3 L mol,1 min,1], and the monomer conversion obeyed the first-order kinetic equation. These observations, along with the successful results in the two-stage polymerization, supported the idea that this polymerization proceeded in a controlled manner. Block copolymerizations of BOT with BTOT were also carried out to afford the corresponding di- and triblock copolymers with narrow molecular weight distributions. The order of the 5% weight loss temperatures was as follows: poly(3-benzyltetrahydro-1,3-oxazolidine-2-thione) [poly(BTOT)] > poly(BTOT54 - b -BOT46) > poly(3-benzyl-1,3-oxazolidine-2-thione) [poly(BOT)]. This indicated that an increase in the BTOT unit content raised the decomposition temperature. The order of the refractive indices was poly(BOT) > poly(BTOT54 - b -BOT46) > poly(BTOT54 - b -BOT46 - b -BTOT50) > poly(BTOT); this was in accord with the order of the sulfur content in the polymer chain. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4795,4803, 2006 [source] Synthesis and properties of polyimides bearing acid groups on long pendant aliphatic chainsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 13 2006Tomohiro Yasuda Abstract A series of novel polyimide electrolytes having long pendant sulfo- or phosphoalkoxy groups were synthesized for fuel-cell applications. Sulfodecyloxy-, phosphodecyloxy-, and sulfophenoxydodecyloxy-substituted benzidine monomers were synthesized from dihydroxybenzidine. These monomers were copolymerized with naphthalene tetracarboxylic dianhydride and fluorenylidene dianiline to give the corresponding polyimides. A flexible, ductile, and self-standing membrane was obtained via casting from the polyimide solution. Because the acid groups were on long pendant side chains and away from the main chains, the polyimide membrane showed improved oxidative and hydrolytic stability in comparison with the polyimides with sulfonic acid groups on the main chains or on the short side chains. High thermal stability (no glass-transition temperature and a decomposition temperature > 200 °C) was also obtained. The polyimide membrane displayed high proton conductivity of 10,1 S cm,1 at 120 °C. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3995,4005, 2006 [source] Hyperbranched polycarbosiloxane with dendritic boron cores: Synthesis, characterization, and structure regulationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2006Jie Kong Abstract The synthesis, characterization, and structure regulation of hyperbranched polycarbosiloxane with dendritic boron cores were realized in this paper. First, dendritic boron core was synthesized via hydroboration with borane dimethylsulfide and bis(allyloxy)dimethylsilane. Then, the hyperbranched polycarbosiloxanes with dendritic boron cores were synthesized via hydrosilylation with AB2 type monomer of bis(allyloxy)methylsilane and dendritic boron cores. The molecular structures of the dendritic boron core and resulting hyperbranched polymers were characterized by using Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance, and 13C nuclear magnetic resonance spectroscopies. Size exclusion chromatography/multiangle laser light scattering analysis reveals that the structures of hyperbranched polycarbosiloxane can be regulated effectively by incorporation of functional dendritic boron cores. Compared with hyperbranched polycarbosiloxane of the same molecular weight level, the hyperbranched polycarbosiloxane with dendritic boron cores presents narrower molecular weight distribution as well as much smaller hydrodynamic radius and intrinsic viscosity. Thermalgravimetric analyzer analysis indicates that both the decomposition temperature and ceramic yields are increased as the results of the incorporation of dendritic boron cores into hyperbranched polycarbosiloxane. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3930,3941, 2006 [source] Synthesis and characterization of carbon nanotube/polypyrrole core,shell nanocomposites via in situ inverse microemulsionJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 23 2005Yijun Yu Abstract We demonstrate here a feasible approach to the preparation of multiwalled carbon nanotube (MWNT)/polypyrrole (PPy) core,shell nanowires by in situ inverse microemulsion. Transmission electron microscopy and scanning electron microscopy showed that the carbon nanotubes were uniformly coated with a PPy layer with a thickness of several to several tens of nanometers, depending on the MWNT content. Fourier transform infrared spectra suggested that there was strong interaction between the ,-bonded surface of the carbon nanotubes and the conjugated structure of the PPy shell layer. The thermal stability and electrical conductivity of the MWNT/PPy composites were examined with thermogravimetric analysis and a conventional four-probe method. In comparison with pure PPy, the decomposition temperature of the MWNT/PPy (1 wt % MWNT) composites increased from 305 to 335 °C, and the electrical conductivity of the MWNT/PPy (1 wt % MWNT) composites increased by 1 order of magnitude. The current,voltage curves of the MWNT/PPy nanocomposites followed Ohm's law, reflecting the metallic character of the MWNT/PPy nanocomposites. The cyclic voltammetry measurements revealed that PPy/MWNT composites showed an enhancement in the specific charge capacity with respect to that of pure PPy. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 6105,6115, 2005 [source] Solid polymer electrolytes III: Preparation, characterization, and ionic conductivity of new gelled polymer electrolytes based on segmented, perfluoropolyether-modified polyurethaneJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2002Chi-Chang Chen Abstract New segmented polyurethanes with perfluoropolyether (PFPE) and poly(ethylene oxide) blocks were synthesized from a fluorinated macrodiol mixed with poly(ethylene glycol) (PEG) in different ratios as a soft segment, 2,4-toluene diisocyanate as a hard segment, and ethylene glycol as a chain extender. Fourier transform infrared, NMR, and thermal analysis [differential scanning calorimetry and thermogravimetric analysis (TGA)] were used to characterize the structures of these copolymers. The copolymer films were immersed in a liquid electrolyte (1 M LiClO4/propylene carbonate) to form gel-type electrolytes. The ionic conductivities of these polymer electrolytes were investigated through changes in the copolymer composition and content of the liquid electrolyte. The relative molar ratio of PFPE and PEG in the copolymer played an important role in the conductivity and the capacity to retain the liquid electrolyte solution. The copolymer with a 50/50 PFPE/PEG ratio, having the lowest decomposition temperature shown by TGA, exhibited the highest ionic conductivity and lowest activation energy for ion transportation. The conductivities of these systems were about 10,3 S cm,1 at room temperature and 10,2 S cm,1 at 70 °C; the films immersed in the liquid electrolyte with an increase of 70 wt % were homogenous with good mechanical properties. © 2002 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 486,495, 2002; DOI 10.1002/pola.10119 [source] Organosoluble and transparent polyimides derived from alicyclic dianhydride and aromatic diaminesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 1 2002J. G. Liu Abstract Organosoluble polyimides were synthesized with the alicyclic dianhydride 1,8-dimethylbicyclo[2,2,2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride and aromatic diamines. The polyimides possessed good solubility both in strong dipolar solvents and in common solvents; the thermal decomposition temperature of the polyimides exceeded 420 °C. Strong and flexible films of the polyimides, with the cutoff of ultraviolet,visible absorption lower than 310,320 nm, exhibited good features as the alignment layers for nematic liquid crystals with pretilt angles of 1.5,2.9°. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 110,119, 2002 [source] Preparation and Properties of PVC Ternary Nanocomposites Containing Elastomeric Nanoscale Particles and Exfoliated Sodium-MontmorilloniteMACROMOLECULAR MATERIALS & ENGINEERING, Issue 6 2006Qingguo Wang Abstract Summary: A novel rigid PVC ternary nanocomposite containing NBR-ENP and untreated Na-MMT has been fabricated. X-ray diffraction XRD, TEM and SEM observations revealed that the untreated Na-MMT was exfoliated and most NBR-ENPs (about 90 nm) were separately dispersed in the PVC matrix. DMTA and TGA demonstrated that the PVC ternary nanocomposites had a higher glass transition temperature and a higher decomposition temperature than neat PVC, while the toughness increased simultaneously. Combustion tests showed that the exfoliated clay in the PVC/NBR-ENP/MMT ternary nanocomposites did not improve the flame retardancy after ignition under strong heat flux. Schematic diagram of the fabrication procedure of PVC/NBR-ENP/Na-MMT ternary nanocomposites. [source] New organosoluble polyimides with low dielectric constants derived from bis[4-(2-trifluoromethyl-4-aminophenoxy)phenyl] diphenylmethyleneMACROMOLECULAR SYMPOSIA, Issue 1 2003Der-Jang Liaw Abstract A new kink diamine with trifluoromethyl group on either side, bis[4-(2-trifluoromethyl-4-aminophenoxy)phenyl]diphenylmethane(BTFAPDM), was reacted with various aromatic dianhydrides to prepare polyimides via poly (amic acid) precursors followed by thermal or chemical imidization. Polyimides were prepared using 3,3,, 4,4,-biphenyltetracarboxylic dianhydride(1), 4,4,-oxydiphthalic anhydride(2), 3,3,,4,4,-benzophenonetetracarboxylic dianhydride (3), 4,4,-sulfonyldiphthalic anhydride(4), and 4,4,-hexafluoroisopropylidene-diphathalic anhydride(5). The fluoro-polyimides exhibited low dielectric constants between 2.46 and 2.98, light color, and excellent high solubility. They exhibited glass transition temperatures between 227 and 253°C, and possessed a coefficient of thermal expansion (CTE) of 60-88 ppm/°C. Polymers PI-2, PI-3, PI-4, PI-5 showed excellent solubility in the organic solvents: N -methyl-2-pyrrolidinone (NMP), N,N -dimethylacetamide (DMAc), N,N -dimethylformamide (DMF), dimethyl sulfoxide (DMSO), pyridkie and tetrahydrofuran (THF). Inherent viscosity of the polyimides were found to range between 0.58 and 0.72 dLg-1. Thermogravimetric analysis of the polyimides revealed a high thermal stability decomposition temperature in excess of 500°C in nitrogen. Temperature at 10 % weight loss was found to be in the range 506-563°C and 498-557°C in nitrogen and air, respectively. The polyimide films had a tensile strength in the range 75-87 MPa; tensile modulus, 1.5-2.2 GPa; and elongation at break, 6-7%. [source] Nanoclay-reinforced syntactic foams: Flexure and thermal behaviorPOLYMER COMPOSITES, Issue 8 2010Mrinal C. Saha Syntactic foams containing 60 vol% of hollow glass microballoons in epoxy matrix are modified with untreated nanoclays using combined mechanical and ultrasonication methods. Effects of nanoclays on flexure and thermal behavior of syntactic foams are investigated by adding different amount of nanoclays in the range of 1,3% by weight. Microscopic examinations and physical property characterization are performed to determine the interactions among constituent materials and the void formation during fabrication. It is found that the syntactic foams with 2 wt% nanoclays show the highest improvement in flexural properties (,42% strength and ,18% modulus) and dynamic mechanical properties (,30% storage modulus and ,28% loss modulus) properties. Thermal decomposition temperature is found to be unaffected by the addition of nanoclays, whereas a continuous reduction in the coefficient of thermal expansion (CTE) is observed. An examination of failure surface indicates that the failure is initiated on the tension side of the flexure sample due to fracturing of microballoons. POLYM. COMPOS., 31:1332,1342, 2010. © 2009 Society of Plastics Engineers [source] Rheology and melt strength of long chain branching polypropylene prepared by reactive extrusion with various peroxidesPOLYMER ENGINEERING & SCIENCE, Issue 2 2010Feng-Hua Su Long Chain Branching Polypropylenes were prepared in an extruder by a melt grafting reaction in the presence of various peroxides and a polyfunctional monomer of 1,6-hexanediol diarylate. Fourier Transformed Infrared spectra and the rheological characteristics indicated that the grafting reaction added long branched chains to linear polypropylene (PP). In comparison to the initial PP, the branched samples exhibited higher melt strength, lower melt flow index, and enhancement of crystallization temperature. The branching number of the modified samples agreed well with their melt viscoelasticity and the improved degree of their melt strength. The branching level in modified PPs could be controlled by the property and structure of the peroxide used. Peroxides with lower decomposition temperature and more stable radicals after decomposition promoted the branching reaction, leading to the modified PPs with higher branching level and melt strength. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers [source] The effect of copper(II) on the thermal and mechanical properties of poly(vinyl alcohol)/silica hybridPOLYMER ENGINEERING & SCIENCE, Issue 8 2009Juan Li A novel copper-poly(vinyl alcohol) (PVA)/silica complex was prepared and its chemical structure, thermal, and mechanical properties were studied. The results showed that the crystallinity of PVA first increased and then decreased by the addition of copper chloride, whereas, the thermal decomposition temperature increased dramatically. For PVA/silica hybrid, the decomposition temperature associated with the removal of water molecules in PVA chains was 262°C. But the temperature increased to 361°C when the content of copper chloride was 2 wt%. The intelligent electronic tensile tester was used to investigate the mechanical properties of these complexes. The results suggested that the tensile strength of the complexes is improved with negligible decrease in the plasticity. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers [source] Preparation and characterization of polyurethane,gold nanocomposites prepared using encapsulated gold nanoparticlesPOLYMER INTERNATIONAL, Issue 7 2010Chao-Ching Chang Abstract Gold nanoparticles (GNPs) have been widely studied due to their unique properties. Although many research groups have developed the synthesis of GNPs using various polymers as stabilizing or reducing agents, the effects of GNPs on the structures and properties of polymer matrices have been less reported. We propose a new design for the preparation of polyurethane,gold (PU,Au) nanocomposites. 11-Mercapto-1-undecanol-coated GNPs acted as the chain extenders and reacted with isocyanates to form covalent bonds between PU and GNPs. PU,Au nanocomposites were successfully synthesized, and the effects of multifunctional GNPs on the structures, morphology and properties of poly(ester urethane) were investigated. Scanning electron microscopy images suggested the GNPs can be dispersed uniformly in the PU matrix. Maltese-cross of spherical crystals was observed in the PU,Au nanocomposites, and the size of the crystals decreased with an increase in gold content. As the gold content increased, the thermal decomposition temperature and the temperature of the maximum decomposition rate increased. The glass transition temperature, crystal melting temperature and melting enthalpy of the soft segment also increased progressively. The results showed that multifunctional GNPs concentrated hard segments and resulted in an increase of heterogeneous nucleation, phase separation and elasticity. Copyright © 2010 Society of Chemical Industry [source] | |||||||||||||