共查询到20条相似文献,搜索用时 15 毫秒
1.
E.G. Merino S. Atlas M. Raihane A. Belfkira M. Lahcini A. Hult M. Dionísio N.T. Correia 《European Polymer Journal》2011,(7):1429-1446
Aiming to develop new dielectric polymers containing CN and F groups with strong dipole moments, a novel copolymer of acrylonitrile (AN) and 2,2,2-trifluoroethyl acrylate (ATRIF) was synthesized in acetonitrile by free radical process as well as the respective homopolymer (poly(ATRIF)). The copolymer’s composition and microstructure were analyzed by FTIR, 1H and 13C NMR spectroscopy and SEC. The molar incorporation of AN determined in the copolymer by NMR was 58 mol%. Thermogravimetric analysis of poly(AN-co-ATRIF) copolymer showed good thermal stability comparatively to the fluorinated homopolymer.Both copolymer, poly(AN-co-ATRIF), and homopolymer, poly(ATRIF), were dielectrically characterized over a frequency range from 10−1 to 106 Hz, and in a temperature range from 223 to 393 K. The dominating relaxation process detected in both materials is the α-relaxation, associated with the dynamic glass transition. A VFTH temperature dependence of the relaxation times (τ) was found for both materials, as characteristic of cooperative processes, from which the respective glass transition temperatures (Tg(τ = 100 s)) were estimated, which differ ∼40 K, the one of the copolymer being higher (307 K) in accordance to the calorimetric analysis. This effect was attributed to a higher stiffness of the backbone in the copolymer originated by the inclusion of the acrylonitrile groups. Both relaxation functions have the same breath of relaxation times allowing constructing a single master curve, indicating similar non-exponential character. A less fragile behavior was found for the copolymer. This was rationalized in a more straightforward way by the free volume approach instead from a correlation between fragility and intermolecular coupling. It was found that in the copolymer the free volume increases at a lower rate with the temperature increase. It was inferred from the VFTH temperature dependence of the dc conductivity and low values of the decoupling index that ion motion is significantly influenced by the dynamics of the α-process. 相似文献
2.
E.El Shafee 《European Polymer Journal》2002,38(3):413-421
Binary blends of atactic poly(epichlorohydrin) (aPECH) and poly(3-hydroxybutyrate) (PHB) were investigated as a function of blend composition and crystallization conditions by dielectric relaxation spectroscopy. The quenched samples were found to be miscible in the whole composition range by detecting only one glass transition relaxation, for each composition, which could be closely described by the Gorden-Taylor equation. The cold-crystallized blends displayed two glass transition relaxations at all blend ratios indicating the coexisting of two amorphous populations: a pure aPECH phase dispersed mainly in the interfibrillar zones and a mixed amorphous phase held between crystal lamellae. The interlamellar trapping of aPECH was small and decreases with increasing the overall PHB content in the blend. At high crystallization temperatures the aPECH molecules was found to reside mainly in the interfibrillar regions due to its high mobility relative to the crystal growth rate of PHB. Our results suggest that because the intersegmental interaction in aPECH/PHB blends is weak, the mobility of the amorphous component at a given crystallization temperature decides diluent segregation. 相似文献
3.
The idea of coexistence of two different amorphous fractions in semi-crystalline poly(ethylene) (PE) is taken into consideration. Differential scanning calorimetry, dynamic mechanical thermal analysis and positron annihilation were used to study the effect of supermolecular structure on the glass transition associated with ‘semi-ordered’ amorphous phase. The arrangement of chains, located in this phase, is forced internally by the presence of crystalline domains. Influence of drawing, irradiation and annealing on thermodynamic and structural parameters was investigated. In a series of experiments the correlation between the glass transition, the α relaxation and the free volume of a semi-crystalline system was found. In order to better describe the relaxation, existence of two types of amorphous fractions was assumed. The relaxations are treated as a long-scale motion of macromolecule segments located into the ‘semi-ordered’ amorphous regions, or into the ‘real’ amorphous regions, and are labelled as αc and αg, respectively. The magnitudes of the loss peaks were quite sensitive to the free volume, which was found to increase by drawing and decrease by irradiation. Two different DSC traces were recorded for both glass transitions. 相似文献
4.
The dielectric properties of methylacrylate (MA)/tri-ethyleneglycol dimethacrylate (TrEGDMA) copolymers at different compositions, ranging from 0 to 100, were measured between −120 and 150 °C over the frequency range 0.1 Hz-1 MHz. In the given frequency range, three relaxation processes were detected by dielectric relaxation spectroscopy in homo poly-TrEGDMA and copolymers: the α process associated with the glass transition, and two secondary processes due to localized mobility. In PMA only one secondary process was observed besides the alpha relaxation process. The influence of copolymerization going from PMA, monofunctional softer component with a glass transition determined calorimetrically as 284 K, to poly-TrEGDMA, higher glass transition component, bifunctional, that also forms a dense network due to cross linking, reflects mainly in the alpha process that shifts to higher temperatures and becomes broader. The raise and broadening in the glass transition with TrEGDMA increase was also observed by dynamic mechanical thermal analysis and differential scanning calorimetry. The glass transition temperature of poly-TrEGDMA was not detected calorimetrically but a value of 429 K was estimated from the best fit of the Fox equation. In what concerns the secondary relaxation process detected in poly-TrEGDMA and copolymers at the lowest temperatures, it is related with local twisting motions of ethyleneglycol moieties, being designated as γ relaxation, while the process detected in the medium temperature range is associated with the rotation of the carboxylic groups as in poly(alkyl methacrylates), designated as β relaxation. This process is detected at much lower temperatures in homo PMA in the same temperature region than the above mentioned γ relaxation. The copolymerization influences mainly the α process while the γ process remains almost unaffected in copolymers relative to homo poly-TrEGDMA. The β process is largely determined by the presence o the tri-ethylene glycol dimethacrylate monomeric units even in copolymers with the lowest TrEGDMA content. 相似文献
5.
M. Wübbenhorst A. L. de Rooij J. van Turnhout J. Tacx V. Mathot 《Colloid and polymer science》2001,279(6):525-531
A curious, strong dielectric relaxation process (δ) was found in rapidly cooled poly(ethylene naphthalate). This process,
which is located between two known β and β* relaxations of PEN, appears predominantly after rapid cooling and remains present
even after heating above the glass transition temperature. In view of its very low activation energy of ∼10 kJ/mol, its markedly
high relaxation strength of up to Δɛ=5, and its Debye-like peak shape, a collective relaxation mechanism is proposed, which
involves collective crankshaft motions of the -O-CH2-CH2-O- sequences in a regular arrangement of the main chains. The analogy between this δ-relaxation and an ultra-slow relaxation
recently found in the smectic E phase of a side-chain liquid crystalline polymer suggests a (close-to) hexagonal smectic ordering
in PEN. The very existence of liquid-crystalline order in PEN is corroborated by the observation of a thermo-reversible discontinuity
in the relaxation parameters around −90 °C, which resembles a broadened LC-LC phase transition. Re-evaluation of experimental
data of the β* relaxation, which occurs in the non-crystalline fraction of PEN, suggests that this relaxation is sensitive
to the local orientational order, which extends from nematic to isotropic. The shift in the temperature of the β* peak and
even the splitting of this peak found by other authors can be ascribed to the lowering of the activation energy by the local
ordered packing of the PEN chains in line with a lower activation energy in the nematic order. The coexistence of isotropic
and nematic regions in PEN is put in the context of orientational order fluctuations during the induction period of cold crystallisation
of semi-flexible polymers.
Received: 31 August 2000 Accepted: 30 October 2000 相似文献
6.
Dielectric relaxation spectroscopy was used to investigate the effect of the inorganic phase on the polymeric relaxation dynamics in PMMA/silica hybrids synthesized in situ via sol-gel processes. It was found that the large-scale molecular motions of PMMA were influenced by the addition of silica, inducing longer mean relaxation times, more heterogeneous relaxing environments and the higher activation energy. Explanations based on hydrogen-bond interactions between two phases and a fraction of entrapped chain segments in silica networks were proposed to understand the influence of the silica. 相似文献
7.
Glass transitions were observed in thin films of poly(2-vinyl pyridine) (P2VP) and poly(methyl methacrylate) (PMMA) using a scanning nanocalorimetry technique which has both high sensitivity (10−9 J/K) and high scan rates (104-105 K/s). Samples were deposited by the spin-cast method. The thickness of samples was 100-400 nm. Glass transition temperature, obtained by nanocalorimetry, is shifted toward higher temperatures by 10-20 K and activation enthalpy of glass transition is shifted to lower values by factor of 2-4. The glass transition characteristics of both polymers are discussed in terms of the standard Tool-Narayanaswamy-Moynihan (TNM) multi-parameter model. 相似文献
8.
To study the ion‐conductive and dielectric properties of polymer electrolytes based on poly(ethylene carbonate) (PEC) with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), the complex permittivity and conductivity were measured using broadband dielectric spectroscopy. The temperature dependence of the relaxation frequency and ionic conductivity for PEC‐LiTFSI electrolytes (1 – 200 mol%) indicates that the segmental motion of PEC chains decreases with the addition of just 1 mol% of Li salt and increases with increasing concentration above 10 mol%. According to the Walden rule for PEC‐based electrolytes, the value of deviation from the reference line increased, and the fragility and decoupling exponents decreased with increasing salt concentration. These results indicate that there are large numbers of ion pairs and aggregated ions, which imply low ionicity and reduced fragility in highly concentrated PEC‐based electrolytes. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
9.
Temperature-induced phase transition in water solutions of poly(N-isopropylacrylamide) (PNIPAM) and poly(N-isopropylmethacrylamide) (PNIPMAM) have been studied by ATR FTIR and Raman spectroscopy in combination with quantum chemical calculations. The presence or absence of the α-methyl group has a strong effect on the physical structure of water solutions. Although the hydrophobic interactions for PNIPMAM and PNIPAM are very similar, PNIPMAM with additional methyl group exhibits significantly weaker intermolecular interactions between the amide groups. That effect is the cause of the higher transition temperature Tt by about 8 °C for PNIPMAM compared to PNIPAM due to the formation of larger compact structures. The presence of the methyl group is significant for the reversibility of the temperature transition during the backward cooling as the dissolution of more stable compact PNIPMAM requires overcoming of a higher energy barrier and shows a strong hysteresis. 相似文献
10.
New poly(benzoxazole–imide)s have been prepared by polycondensation of bis(o-aminophenol)s, such as 3,3′ dihydroxybenzidine or 2,2-bis(3-amino-4-hydroxyphenyl)-hexafluoropropane, with diacid chlorides containing both imide and hexafluoroisopropylidene groups. The soluble polymer precursor resulting from the first step of polycondensation in N-methylpyrrolidinone (NMP) at low temperature was processed into thin flexible films, which were then thermally treated to reach the fully cyclized structure of poly(benzoxazole–imide)s, as observed by infrared spectra. An alternative way to produce the cyclization was by heating at reflux the solution of polymer precursor in NMP. Thermal stability, glass transition temperature, dielectric constant and its dependence on relative humidity have been studied and compared with those of related polybenzoxazoles and other heterocyclic Polymers. 相似文献
11.
We report on the spectroelectrochemical characterization of conducting polymer (CP) films, composed of alternating layers of poly(aniline) (PANI) and poly(acrylic acid) (PAA), deposited on ITO-coated, planar glass substrates using layer-by-layer self-assembly. Absorbance changes associated with voltammetrically induced redox changes in ultrathin films composed of only two bilayers (ITO/PANI/PAA/PANI/PAA) were monitored in real time using a unique multiple reflection, broadband attenuated total reflection (ATR) spectrometer. CP films in contact with pH 7 buffer undergo a single oxidation/reduction process, with ca. 12.5% of the aniline centers in the film being oxidized and reduced. The ATR spectra indicate that during an anodic sweep, the leucoemeraldine form of PANI in these films is oxidized to generate both the emeraldine and pernigraniline forms simultaneously. A comparison of the behavior observed during anodic and cathodic sweeps suggests that the rate of oxidation is limited by structural changes in the polymer film originating in electrostatic repulsion between positively charged PANI chains. 相似文献
12.
Francesc Estrany David Aradilla Ramn Oliver Elaine Armelin Carlos Alemn 《European Polymer Journal》2008,44(5):1323-1330
Multilayered films formed by 3, 5 and 7 alternated layers of poly(3,4-ethylenedioxythiophene) and poly(N-methylpyrrole) have been prepared by chronoamperometry under a constant potential of 1.4 V using a layer-by-layer electrodeposition technique. In order to examine influence of the interface:bulk dimensional ratio, the thickness of the yielded films was reduced from the submicrometric to the nanometric scale by decreasing the polymerization time of each layer from 100 s to 10 s. The electroactivity, electrochemical characteristics and morphologies of the resulting multilayered films have been compared with those obtained for both single-component poly(3,4-ethylenedioxythiophene) films prepared using identical experimental conditions and previously reported multilayered films with thickness within the micrometric scale [Estrany F, Aradilla D, Oliver R, Alemán C. Eur Polym J 2007;43:1876]. 相似文献
13.
A. Kyritsis A. Spanoudaki C. Pandis L. Hartmann R. Pelster N. Shinyashiki J.C. Rodríguez Hernández J.L. Gómez Ribelles M. Monleón Pradas P. Pissis 《European Polymer Journal》2011,47(12):2391-2402
Water and polymer dynamics in hydrogels based on random copolymers of hydrophilic poly(hydroxyl ethyl acrylate) (PHEA) and hydrophobic poly(ethyl acrylate) (PEA), in wide ranges of composition, were investigated by means of two dielectric techniques, thermally stimulated depolarization currents (TSDC) and, mainly, broadband dielectric relaxation spectroscopy (DRS) at several levels of relative humidity/water content. Water sorption of the hydrogels was studied by equilibrium sorption isotherms (ESI). Two secondary relaxations (γ and βsw) and the primary (segmental) α relaxation associated with the glass transition of the copolymer matrix were followed and analyzed against copolymer composition and water content. The results show that the copolymers are homogeneous at nm scale, except at very high PEA content. Correlations were observed between results on the organization of water in the hydrogels and on water effects on polymer dynamics. Distinct changes in the dielectric response, in particular in the time scale and the dielectric strength of the βsw relaxation, at the water content of the completion of the first hydration layer indicate that water molecules themselves contribute to the dielectric response at higher water contents. Proton conductivity of the hydrogels at various levels of water content was also studied and correlation to segmental dynamics (decoupling) was analyzed. 相似文献
14.
Measurements of the complex relative permittivity of poly(vinyl acetate) from 35 °C to 190 °C and poly(vinyl chloride) from 90 °C to 150 °C in the frequency range 10–2 –107 Hz and the pressure range 1–5000 bar are reported. Details of the pressure generating system and of the dielectric equipment are described. 相似文献
15.
交联聚醚聚氨酯的表征及其聚集态转变和自由体积特性的正电子湮没研究 总被引:1,自引:0,他引:1
采用全反射红外光谱(ATR-IR)对聚合物的结构进行了表征,证明其为交联聚醚聚氨酯(PEU),且其碱金属盐络合物的导电性与其自由体积有关。在110~350K温度范围内测量了PEU的正电子湮没寿命谱,结果表明正电子湮没寿命谱的温度关系可灵敏地反映聚合物的聚集态转变及其自由体积特性随温度的变化。得到了PEU的次级转变、玻璃化转变及结晶相的熔融变化等方面的信息。并由实验测得的o-Ps寿命计算出不同温度下PEU中自由体积孔洞的尺寸。 相似文献
16.
Ken-ichi Kato Kaori Ito-Akita Hiroyuki Ohno 《Journal of Solid State Electrochemistry》2000,4(3):141-145
Poly(ethylene oxide) (PEO) oligomers having alkali metal thiolate groups on the chain ends (PEO
m
-S−M+) were prepared as an ion conductive matrix. The molecular weight of the PEO part (m) and the content of the thiolate groups in the molecule were changed to analyze the effect of carrier ion concentration in
the bulk. In a series of potassium salt derivatives, PEO350-SK showed the highest ionic conductivity of 6.42 × 10−5 S/cm at 50 °C. In spite of a poor degree of dissociation which was derived from the acidity of the thiolate groups, PEO
m
-SM showed quite high ionic conductivity among other PEO/salt hybrids. PEO
m
-SM had glass transition temperatures (T
g) 20 °C lower than other PEO/salt hybrids. Lowering the T
g was concluded to be effective in providing higher ionic conductivity for PEO-based polymer electrolytes.
Received: 30 April 1999 / Accepted: 20 June 1999 相似文献
17.
A novel type of a Si-containing poly(urethane-imide) (PUI) was prepared by two different methods. In the first method, Si-containing polyurethane (PU) prepolymer having isocyanate end groups was prepared by the reaction of diphenylsilanediol (DSiD) and toluene diisocyanate (TDI). Subsequently the PU prepolymer was reacted with pyromellitic dianhydride (PMDA) or benzophenonetetracarboxylic dianhydride (BTDA) in N-methyl pyrolidone (NMP) to form Si-containing modified polyimide directly. In the second method, PU prepolymer was reacted with diaminodiphenylether (DDE) or diaminodiphenylsulfone (DDS) in order to prepare an amine telechelic PU prepolymer. Finally, the PU prepolymer having diamine end groups was reacted with PMDA or BTDA to form a Si-containing modified polyimide. Cast films prepared by second method were thermally treated at 160 °C to give a series of clear, transparent PUI films. Thermogravimetric analysis indicated that the thermal degradation of PUI starts at 265 °C which is higher than degradation temperature of conventional PU, confirming that the introduction of imide groups improved the thermal stability of PU.To characterize the modified polyimides and their films, TGA, FTIR, SEM and inherent viscosity analyses were carried out. The dielectrical properties were investigated by the frequency-capacitance method. Dielectric constant, dielectric breakdown strength, moisture uptake and solubility properties of the films were also investigated. 相似文献
18.
To assess the compatibility of blends of synthetic poly(propylene carbonate) (PPC), with a natural bacterial poly(3-hydroxybutyrate) (PHB), a simple casting procedure of blend was used. poly(3-hydroxybutyrate)/poly(propylene carbonate) blends are found to be incompatible according to DSC and DMA analysis. In order to improve the compatibility and mechanical properties of PHB/PPC blends, poly(vinyl acetate) (PVAc) was added as a compatibilizer. The effects of PVAc on the thermal behavior, morphology, and mechanical properties of 70PHB/30PPC blend were investigated. The results show that the melting point and the crystallization temperature of PHB in blends decrease with the increase of PVAc content in blends, the loss factor changes from two separate peaks of 70PHB/30PPC blend to one peak of 70PHB/30PPC/12PVAc blend. It is also found that adding PVAc into 70PHB/30PPC blend can decrease the size of dispersed phase from morphology analysis. The result of tensile properties shows that PVAc can increase the tensile strength and Young’s modulus of 70PHB/30PPC blend, and both the elongation at break and the tensile toughness increase significantly with PVAc added into 70PHB/30PPC. 相似文献
19.
A new double perovskite oxide holmium magnesium zirconate Ho2MgZrO6 (HMZ) was prepared by solid state reaction technique. The crystal structure has been determined by powder X-ray diffraction which shows monoclinic phase at room temperature with cell parameters a = 9.3028 ± 0.0030 Å, b = 5.2293 ± 0.0008 Å, c = 4.4009 ± 0.0009 Å, β = 103.3746 ± 0.0166°. An analysis of complex permittivity with frequency was carried out assuming a distribution of relaxation times. The frequency dependent electrical data are analyzed in the framework of conductivity and electric modulus formalisms. At the high temperature range, conductivity data satisfy the variable range hopping (VRH) model. In this regime, the conductivity of sample obeys Mott’s T1/4 law, characteristic of VRH. High temperature data indicates the formation of thermally activated small polarons. The scaling behaviour of imaginary part of electric modulus suggests that the relaxation describes the same mechanism at various temperatures. 相似文献
20.
The heat capacity, Cp, of poly(oxyethylene), POE, with a molar mass of 900,000 Da, was analyzed by temperature-modulated differential scanning calorimetry, TMDSC. The high molar mass POE crystals are in a folded-chain macroconformation and show some locally reversible melting, starting already at about 250 K. At 335 K the thermodynamic heat capacity reaches the level of the melt. The end of melting of a high-crystallinity sample was analyzed quasi-isothermally with varying modulation amplitudes from 0.2 to 3.0 K to study the reversible crystallinity. A new internal calibration method was developed which allows to quantitatively assess small fractions of reversibly melting crystals in the presence of the reversible heat capacity and large amounts of irreversible melting. The specific reversibility decreases to small values in the vicinity of the end of melting, but does not seem to go to zero. The reversible melting is close to symmetric with a small fraction crystallizing slower than melting, i.e., under the chosen condition some of the melting and crystallization remains reversing. The collected data behave as one expects for a crystallization governed by molecular nucleation and not as one would expect from the formation of an intermediate mesophase on crystallization. The method developed allows a study of the active surface of melting and crystallization of flexible macromolecules. 相似文献