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Differential Scanning Calorimetry Results (differential + scanning_calorimetry_result)
Selected AbstractsEffect of addition of organic microspheres on proton conductivity property of sulfonated poly(arylene ether sulfone) membraneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Cui Liang Abstract Sulfonated poly(arylene ether sulfone) (SPAES)/polystyrene(PS) and SPAES/polystyrene sulfonic acid (PSSA) composite membranes were studied for a proton-exchange membrane used in a fuel cell. PS microspheres were synthesized by emulsion polymerization. PSSA microspheres with 5.3 mmol/g ion-exchange capacity (IEC) were prepared by sulfonation of PS microspheres. The composite membranes were prepared by solution casting. SPAES/PSSA composite membranes showed higher proton conductivity than a SPAES membrane because of the IEC improved by adding PSSA. Although the addition of PSSA also brought about the increase of a methanol permeability, the proton/methanol selectivity defined as the ratio of the proton conductivity to the methanol permeability was improved at low humidity by adding 5 wt % of PSSA microspheres. Differential scanning calorimetry results indicated that the amount of free water varied in the cases of the addition of the two kinds of organic microspheres. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Thermal properties and phase morphology of melt-mixed poly(trimethylene terephthalate)/poly(hexamethylene isophthalamide) blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Fang-Chyou Chiu Abstract This work examines the thermal properties and phase morphology of melt-mixed poly(trimethylene terephthalate) (PTT)/poly(hexamethylene isophthalamide) (PA 6I) blends. Two temperatures, i.e., 250 and 260°C, are used to prepare the blends, respectively. Differential scanning calorimetry results indicate the immiscible feature of the blends. It is thus concluded that the ester-amide interchange reaction hardly occurred in the PTT/PA 6I blends. Depending on the composition and mixing temperature, the crystallization ability of PTT in the blends is either enhanced or hindered. Basically, a lower PA 6I content shifts the PTT melt crystallization to a higher temperature, whereas a higher PA 6I content causes an opposing outcome. The original complex melting behavior of neat PTT becomes more regular after the incorporation of 60 wt % or 80 wt % of PA 6I. Thermogravimetry analyses (TGA) show that the thermal stability of the blends improves as the PA 6I content increases. The two-phased morphology of the blends is examined by scanning electron microscopy (SEM). Polarized light microscopy (PLM) results reveal that the PTT spherulites become coarser with the inclusion of PA 6I; only smaller/dispersed crystallites are observed in the blend with 20 wt % of PTT. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Proton transportation in an organic,inorganic hybrid polymer electrolyte based on a polysiloxane/poly(allylamine) networkJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 15 2005Ping-Lin Kuo Abstract A new class of proton-conducting polymer was developed via the sol,gel process from amino-containing organic,inorganic hybrids by the treatment of poly(allylamine) with 3-glycidoxypropyltrimethoxysilane doped with ortho -phosphoric acid. The polymer matrix contains many hydrophilic sites and consists of a double-crosslinked framework of polysiloxane and amine/epoxide. Differential scanning calorimetry results suggest that hydrogen bonding or electrostatic forces are present between H3PO4 and the amine nitrogen, resulting in an increase in the glass-transition temperature of the poly(allylamine) chain with an increasing P/N ratio. The 31P magic-angle spinning NMR spectra indicate that three types of phosphate species are involved in the proton conduction, and the motional freedom of H3PO4 is increased with increasing P/N ratios. The conductivity above 80 °C does not drop off but increases instead. Under a dry atmosphere, a high conductivity of 10,3 S/cm at temperatures up to 130 °C has been achieved. The maximum activation energy obtained at P/N = 0.5 suggests that a transition of proton-conducting behavior exits between Grotthus- and vehicle-type mechanisms. The dependence of conductivity on relative humidity (RH) above 50% is smaller for H3PO4 -doped membranes compared with H3PO4 -free ones. These hybrid polymers have characteristics of low water content (23 wt %) and high conductivity (10,2 S/cm at 95% RH), making them promising candidates as electrolytes for fuel cells. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3359,3367, 2005 [source] Synthesis and Monitoring of ,-Bi2Mo3O12 Catalyst Formation using Thermo-Raman SpectroscopyEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 8 2004Anil Ghule Abstract Thermo-Raman spectroscopy was used to monitor the dehydration and phase transformations of Bi2Mo3O12·5H2O. The hydrated forms Bi2Mo3O12·5H2O, Bi2Mo3O12·4.75H2O, Bi2Mo3O12·3H2O, Bi2Mo3O12·2H2O, and anhydrous Bi2Mo3O12 were observed during dehydration in the wavelength range from 200 to 1400 cm,1. Representative Raman spectra of these compounds are reported for the first time. The thermo-Raman intensity thermogram showed a systematic dehydration in four steps, and the differential thermo-Raman intensity thermogram confirmed this. Thermogravimetry, differential thermogravimetry, and differential scanning calorimetry results were in harmony with the results of the thermo-Raman spectroscopy. Additionally, the dehydration resulting in formation of anhydrous Bi2Mo3O12 (amorphous Bi2Mo3O12 phase) and the final transformation into the ,-Bi2Mo3O12 phase was observed to be a dynamic thermal process. The slow, controlled heating rate produced ,-Bi2Mo3O12 catalyst with a particle size averaging 200 nm. The catalyst formed was further characterized by Fourier transform infrared spectroscopy, X-ray diffraction, time of flight SIMS, transmission electron microscopy, and energy-dispersive X-ray analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] ELECTRICAL CONDUCTIVITY OF HEATED CORNSTARCH,WATER MIXTURESJOURNAL OF FOOD PROCESS ENGINEERING, Issue 6 2009EDUARDO MORALES-SANCHEZ ABSTRACT Electrical conductivity (EC) of cornstarch,water mixtures in the range 10:90 to 70:30 (w/w) was studied as a function of temperature. An external resistive heating system equipped with an electronic device capable of monitoring EC in real time was used and EC of the mixtures was measured while heated at a rate of 5C/min. Results showed that EC went through four different temperature-dependent stages (A, B, C and D). Stage B (41C to 64C) showed a lower EC increasing rate when compared with that of Stage A (from 25C to 41C), probably as a result of starch granule swelling. In Stage C (64C to 78C), EC behavior was found to be dependent on water content. When water content was more than 50%, the value for EC increased. On the other side, EC decreased when water content was less than 50%. Stage C was related to starch gelatinization, according to differential scanning calorimetry results obtained in this study. In Stage D (78C to 92C), a steady increase in EC was observed, probably as a result of the total solubilization of starch in water. It was concluded that Stage C in EC graphs corresponded to cornstarch gelatinization, so it might be possible to use EC monitoring as an alternative technique to measure cornstarch thermal characteristics with different contents of water. PRACTICAL APPLICATIONS Electrical conductivity can be used as an adequate technique to monitor gelatinization, granule swelling and phase change of starch as a function of temperature in corn starch,water mixtures with a wide range of water contents. With this technique, it is also possible to calculate important thermal parameters, such as the beginning and end of the gelatinization and the energy activation for the heating process of cornstarch. This can lead to a better design and control of important industrial corn processes such as alkaline cooking. [source] Preparation and characterization of polypropylene/solid-state organomodified montmorillonite nanocompositesPOLYMER COMPOSITES, Issue 4 2008Sun Yu-hai A novel organomodified montmorillonite prepared by solid-state method and its nanocomposites with polypropylene were studied. The interaction between modifying agent and montmorillonite was investigated by X-ray diffraction (XRD) analysis, contact angle determination, and Fourier-transform infrared spectroscopy. The results showed that the modifying agent behaves as an effective intercalating agent, enlarging the interlayer spacing of montmorillonite and making montmorillonite more hydrophobic. Polypropylene/solid-state organomodified montmorillonite composites were prepared by melt-mixing method. The dispersion of the silicates was investigated by XRD analysis and transmission electron microscopy. It was found that the nanocomposites are formed with solid-state organomodified montmorillonite and polypropylene. The thermogravimetric analysis and differential scanning calorimetry results showed that the organoclay could enhance the thermal stability and decrease the relative crystallinity of polypropylene. Mechanical and rheological tests indicated that the organoclay improves the mechanical properties but has no obvious effect on rheological properties of polypropylene. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers [source] Synthesis and characterization of polyaniline derivative and silver nanoparticle compositesPOLYMER INTERNATIONAL, Issue 10 2008Gururaj M Neelgund Abstract BACKGROUND: There has been a recent surge of interest in the synthesis and applications of electroactive polymers with incorporated metal nanoparticles. These hybrid systems are expected to display synergistic properties between the conjugated polymers and the metal nanoparticles, making them potential candidates for applications in sensors and electronic devices. RESULTS: Composites of polyaniline derivatives,polyaniline, poly(2,5-dimethoxyaniline) and poly(aniline-2,5-dimethoxyaniline),and silver nanoparticles were prepared through simultaneous polymerization of aniline derivative and reduction of AgNO3 in the presence of poly(styrene sulfonic acid) (PSS). We used AgNO3 as one of the initial components (1) to form the silver nanoparticles and (2) as an oxidizing agent for initiation of the polymerization reaction. UV-visible spectra of the synthesized nanocomposites reveal the synchronized formation of silver nanoparticles and polymer matrix. The morphology of the silver nanoparticles and degree of their dispersion in the nanocomposites were characterized by transmission electron microscopy. Thermogravimetric analysis and differential scanning calorimetry results indicate an enhancement of the thermal stability of the nanocomposites compared to the pure polymers. The electrical conductivity of the nanocomposites is in the range 10,4 to 10,2 S cm,1. CONCLUSION: A single-step process for the synthesis of silver nanoparticle,polyaniline derivative nanocomposites doped with PSS has been demonstrated. The approach in which silver nanoparticles are formed simultaneously during the polymerization process results in a good dispersion of the nanoparticles in the conductive polymer matrix. Copyright © 2008 Society of Chemical Industry [source] | |||||||||||||