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  • 1995-1999  (16)
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  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract. The novel poly(aryl ether ketone)s containing chloro-side group were synthesized by nucleophilic substitution reactions of 4,4′-biphenol and chlorohydroquinone with either 4,4′-difluorobenzophenone (BP/CH/DF) or 1,4-bis(p-fluorobenzoyl)benzene (BP/CH/BF) and their thermotropic liquid crystalline properties were characterized by a variety of experimental techniques. The thermotropic liquid crystalline behavior was observed in the copolymers containing 50 and 70% biphenol. Melting transition (Tm) and isotropization transition (Ti) both appeared in the DSC thermograms. A banded texture was formed after shearing the sample in the liquid crystalline state. The novel poly(aryl ether ketone)s had relatively higher glass transition temperature (Tg) in the range of 168 ∼ 200 °C and lower melting temperature (Tm) in the range of 290 ∼ 340 °C. The thermal stability (Td) was in the range of 430 ∼ 490 °C.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly(etheretherketon) (PEEK)/Poly(phenolphthaleinethersulfon) (PPES)-Blockcopolymere mit PPES-Anteilen zwischen 12 und 44% wurden durch Kondensation von fluorterminierten PEEK-Oligomeren und hydroxyterminierten PPES-Oligomeren hergestellt. Die Abhängigkeit der Copolymereigenschaften von der Zusammensetzung wurde untersucht. Die Copolymeren erwiesen sich als homogen, die Komponenten zeigten gute Verträglichkeit ohne Mikrophasenseparation. Die Copolymeren kristallisierten wie PEEK mit rhombischer Struktur. Der Kristallisationsgrad der Copolymeren was gering und nahm mit steigendem PPES-Gehalt rasch ab. Im Ver-gleich zur Kristallstruktur von PEEK wurden für die Längen der a- und b-Achsen des Copolymer-Kristallgitters - und somit auch für das Zellvolumen - größere Werte gefunden. Die Analyse der isothermen Kristallisationskinetik der Copolymeren ergab für den Avrami-Exponenten einen Wert von 2,0. Mit steigendem PPES-Gehalt der Copolymeren erhöhten sich die Glasübergangstemperaturen stark, die thermische Stabilität nahm jedoch ab. Die PEEK/PPES-Blockcopolymeren ziegten gute mechanische Eigenschaften wie hohe Zugfestigkeiten und Elastizitätsmoduli.
    Notes: Poly(ether ether ketone) (PEEK)/poly(phenolphthalein ether sulfone) (PPES) block copolymers were synthesized by a condensation reaction of fluorine-terminated PEEK oligomers and hydroxy-terminated PPES oligomers. The content of PPES in the copolymers was varied from 12 to 44 wt.-%, and the effect of the compositional variation on the properties was investigated. Microphase separation was not observed and the copolymers formed a homogeneous system having good compatibility. The crystal structure of the copolymers is rhombic, equal to PEEK. The degree of crystallinity of the copolymers was low and decreased rapidly with the increase of PPES content. Concerning the cell parameters of the crystalline unit, a- and b-axes are apparently longer and V is, thus, also larger compared with PEEK. Analyses of the isothermal crystallization kinetics of the copolymers provided an Avrami exponent (n) of 2.0. The glass transition temperature (Tg) of the copolymers greatly rose but the thermal stability became much poorer with the increase of PPES content. PEEK/PPES block copolymers possess good mechanical properties such as high strength and modulus.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly(etheretherketon) (PEEK)/4,4′-Dihydroxydiphenylsulfon (DHDPS)-Multiblock-Copolymere mit Diphenyloxysulfon(DPOS)-Gehalten zwischen 4,9 und 36,6 Gew.-% wurden aus DHDPS und fluorterminierten PEEK-Oligomeren hergestellt. Das zahlenmittlere Molekulargewicht (Mn) der PEEK-Oligomeren variierte zwischen 470 und 4900. Der Einfluß der Zusammensetzung auf die Eigenschaften der Copolymeren wurde untersucht. Es wurde keine Mikrophasenseparation beobachtet. Die Copolymeren bildeten ein homogenes System mit guter Phasenverträglichkeit. Bei den Copolymeren mit höchstens 23,1 Gew.-% DPOS wurde eine kristalline Struktur beobachtet. Röntgenweit- und Kleinwinkelstreumessungen ergaben eine rhombische Kristallstruktur, wie sie auch bei PEEK gefunden wird. Die Verteilung der Schichtdicken der kristallinen und amorphen Regionen ist relativbreit. Mit Zunahme des DPOS-Gehalts (oder der Abnahme des zahlenmittleren Molekulargewichts der PEEK-Segmente) nahmen der Kristallinitatsgrad und der Schmelzpunkt der Copolymeren ab, und die Glastemperatur (Tg) nahm schrittweisezu.
    Notes: Poly(ether ether ketone) (PEEK)/4,4′-dihydroxydiphenyl sulfone (DHDPS) multiblock copolymers with a content of the diphenoxysulfone (DPOS) moiety between 4.9 and 36.6wt.-% were synthesized by the reaction of DHDPS and fluorine-terminated PEEK oligomers. The number-average molecular weight of PEEK oligomers (Mn) was varied from 470 to 4900. The effect of the compositional variation on the properties was investigated. Microphase separation was not observed. The copolymers formed a homogeneous system having good compatibility. The copolymers whose DPOS contents are not exceeding 23.1 wt.-% (Mn of PEEK segment ≥ 865) have crystalline structure.From the measurements of wide- and small-angle X-ray scatterings it was revealed that the crystal structure of the copolymers is rhombic, equal to PEEK, and the distribution of the thickness of the crystalline and amorphous regions is very broad. The degree of crystallinity and the melting point of the copolymers decreased and the glass transition temperature (Tg) gradually rose with the increase of the DPOS content (or the decrease of Mn of the PEEK segment).
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 99-105 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Five kinds of poly(aryl ether ketone)s (PAEKs) having para-substituted linear molecular chains were synthesized via nucleophilic substitution reaction of the corresponding difluoro- and dihydroxy-compounds. The glass transition temperature and melting temperature of the PAEKs measured through differential scanning calorimetry in addition to those of other PAEKs reported are approximately proportional to the logarithm of the ratio of the mole fractions of ketone and ether groups in the repeating unit of the PEAKs. On the other hand, this ratio does not affect the crystal structure of the PAEKs.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The evolution of crystallinity and polymorphism during hot-drawing of amorphous poly(ether ether ketone ketone) (PEEKK) as a function of strain rate, draw ratio, and temperature was investigated. In modification I, the competition of chain extension and molecular alignment is responsible for the strain rate and temperature dependence. Modification II crystallization is basically controlled by chain extension during stretching. The former can be transformed into the latter via relaxation during stretching or annealing at elevated temperature.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The novel poly(aryl ether ketone)s were synthesized by nucleophilic substitution reactions of 4,4′-difluorobenzophenone with 4,4′-biphenyldiol and chlorohydroquinone. As expected, the copolymers have lower melting transitions than the biphenyldiol-based homopoly(aryl ether ketone) because of the copolymerization effect of the crystal-disrupting monomer chlorohydroquinone. Copolymers containing 50 and 70% biphenyldiol show two first-order transitions which are associated with the crystal-to-liquid crystal transition and the liquid crystal-to-isotropic transition.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 1643-1650 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of a novel poly(aryl ether ketone) [PEDEKmK] was investigated via polarizing optical microscopy (POM), TEM, DSC, SAXS and electron diffraction (ED). A distinct change in lamellar thickness, orientation, and spherulitic morphology was observed due to crystal melting and recrystallization. However, the crystal packing mode is found to be identical before and after the recrystallization process.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystal structure and polymorphism induced by uniaxial drawing of a poly(aryl ether ketone) [PEDEKmK] prepared from 1,3-bis(4-fluorobenzoyl)benzene and biphenyl-4,4′-diol have been investigated by means of transmission electron microscopy (TEM), electron diffraction (ED), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC) techniques. The melting and recrystallization process in the temperature range of 250-260°C, far below the next melting temperature (306°C), was identified and found to be responsible for the remarkable changes in lamellar morphology. Based on WAXD and ED patterns, it was found that crystal structure of isotropic-crystalline PEDEKmK obtained under different crystallization conditions (melt-crystallization, cold-crystallization, solvent-induced crystallization, melting-recrystallization, and crystallization from solution) keeps the same mode of packing, i.e., a two-chain orthorhombic unit cell with the dimensions a = 0.784 nm, b = 0.600 nm, and c = 4.745 nm (form I). A second crystal modification (form II) can be induced by uniaxial drawing above the glass transition temperature, and always coexists with form I. This form also possesses an orthorhombic unit cell but with different dimensions, i.e., a = 0.470 nm, b = 1.054 nm, c = 5.064 nm. The 0.32 nm longer c -axis of form II as compared with form I is attributed to an overextended chain conformation due to the expansion of ether and ketone bridge bond angles during uniaxial drawing. The temperature dependence of WAXD patterns for the drawn PEDEKmK suggests that form II can be transformed into the more stable form I by relaxation of overextended chains and relief of internal stress at elevated temperature in absence of external tension.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 17 (1996), S. 117-122 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Structures of poly(ether ether ketone ketone)-poly(ether biphenyl ether ketone ketone) copolymers were studied by using small angle X-ray scattering and the one-dimensional electron density correlation function method. The results revealed that structures of the aggregated state of the copolymers depend closely on the biphenyl content (nb). When nb = 0.35, invariant Q, long period L, average thickness of crystal lamellae d̄, electron density difference ηc - ηa and degree of crystallinity Wc, x assume minimum values.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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