ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Polymer and Materials Science  (57)
  • COMMUNICATIONS AND RADAR  (5)
  • 1990-1994  (28)
  • 1980-1984  (34)
  • 1920-1924
Sammlung
Verlag/Herausgeber
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2809-2813 
    ISSN: 0887-624X
    Schlagwort(e): Malachite Green vinyl polymer ; ionic conductivity ; photoinduced switching ; single-ionic ; carrier generation ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Copolymers of bis[4-(N,N-dimethylamino)phenyl]-4-vinylphenylmethanenitrile (vinyl Malachite Green leuconitrile) with methyl methacrylate or ω-methoxyoligo(oxyethylene) methacrylate have been synthesized, aiming at designing one-component-type organic polymers for photoswitchable ion-conducting films. The triphenylmethanenitrile copolymers with ω-methoxyoligo(oxyethylene) methacrylate were found to undergo ionic-conductivity switching by turning on and off UV light at ambient temperature, owing to their low glass transition temperature. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 181-185 
    ISSN: 0887-624X
    Schlagwort(e): poly(bisthiazole-imide) ; heterocyclic polyimide ; solubility ; high-temperature polymers ; thermal properties ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1243-1254 
    ISSN: 0887-624X
    Schlagwort(e): tetraphenylporphyrin-containing polymer ; homopolymer ; water-soluble polymer ; radical polymerization ; manganese(III) complex ; ligand substitution reaction ; anionic ligand ; thiocyanate ; electrostatic effect ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A vinyl monomer containing the pendant tetraphenylporphyrin (TPP) group, 4-vinyltetraphenylporphyrin (VTPP), was synthesized. A homopolymer (PVTPP) which is insoluble in water, and three water-soluble polymers were obtained by radical polymerization. The water-soluble polymers are two anionic polymers (PVPTSPP and PVTPP-StSO3) and a cationic polymer (PVTPP-VPyM). PVPTSPP has sulfonic acid groups in a TPP group and very high charge density. PVTPP-StSO3 was obtained by copolymerization of VTPP and sodium 4-styrenesulfonate. PVTPP-VPyM was obtained by quarternarization of a copolymer of VTPP and 4-vinylpyridine. Polymeric manganese(III) complexes (PMn-VTPP, PMnVPTSPP, PMnVTPP-StSO3, and PMnVTPP-VPyM) were prepared from the polymers and manganese acetate. The acetate ligand in PMnVTPP can be easily substituted by another ligand such as Cl-, AcO-, OH-, and SCN-. The substitution reaction occurs in the interface between water and chloroform. The sulfonated homopolymer, PMnVPTSPP, cannot incorporate with anionic ligands because of the strong electrostatic repulsion. In the anionic copolymer, PMnVTPP-StSO3, the ligand substitution reaction with SCN ligand needs activation energy of 53 kJ/mol. In the cationic polymer complex, PMnVTPP-VPyM, the OH ligand can be easily substituted with the SCN ligand and the equilibrium constant of the reaction was estimated at 1.38 × 10-3. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 777-779 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    Digitale Medien
    Digitale Medien
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 1 (1992), S. 401-413 
    ISSN: 1018-5054
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The conformation of the ethoxy tail flanking the cyanobiphenyl core has been studied in the liquid-crystalline phase as well as in the isotropic solution. In solution, the vicinal coupling constant 3JCH for the moiety CphO—CH (Cph: phenyl carbon) provided the information regarding the rotation around the O—C bond. Phenetole was mostly used as a model compound. The conventional rotational isomeric state (RIS) analysis yielded the energy difference between the gauche and trans state to be of the order of 1,6 to 1,4 kcal/mol in CDCl3, C6D6 and dimethyl-d6 sulfoxide. In this treatment, the rotational state around the neighboring bond (Cph—O) was taken to occur at 0 or π. The deuterated compound, 4-ethoxy-4′-biphenylyl-d7 cyanide, was prepared and studied in the liquid-crystalline state by 2H NMR. The orientational order parameters of the mesogenic core were determined by the analysis of dipolar and quadrupolar splitting data due to aromatic deuterons. The quadrupolar splitting data were also obtained for the deuterated ethoxy tail. The conformation of the tail was elucidated according to the RIS simulation scheme previously proposed. The fraction of the trans conformation ft was estimated to be 0,79 around the nematic-isotropic transition temperature (TNI = 91,9°C). It was suggested that the conformation of the ethoxy tail remains nearly unaffected by the phase transition in the immediate vicinity of TNI. The fraction ft increases moderately toward an asymptotic value as temperature decreases.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 205-208 
    ISSN: 1042-7147
    Schlagwort(e): Polymer electrolytes ; lonic conductivity ; Organogels ; Photopolymerization ; Polyaniline ; Rechargeable battery ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Gel-type solid polymer electrolytes (SPE) which consisted of LiBF4 as the electrolyte, a mixture of propylene carbonate and 1,2-dimethoxyethane as the solvents, and a mixture of ethoxypolyoxyethyleneacrylate and trimethylolpropanetriacrylate as the monomers, were prepared by photopolymerization. The composition range for the gelation and the SPE formation was defined. Relationships between the composition of the SPE, and the ionic conductivity and modulus were clarified. The ionic conductivity of the SPE film, the composition of which was 13 wt% monomer, 20 wt% LiBF4 and 67 wt% solvent, was 2.7 × 10-3 S/cm, and the modulus was 103 dyn/cm2 at 25°C. When a polyaniline(PANI)/SPE interface was formed on polyaniline films by photopolymerization at the optimal composition, the redox behavior of PANI was almost equivalent to that in nonaqueous electrolyte solutions. The discharge capacity of a Li/SPE/PANI film rechargeable battery was 116 mAh/g-PANI (based on the weight of PANI), almost the same as that of a Li/nonaqueous electrolyte solution/PANI cell.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1629-1638 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Blends of poly(ethylene terephthalate) (PET) and a copolyester of bisphenol A-terephthaloylisophthaloyl (PAr) (2:1:1) have been studied both before and after transesterification. The physical blends exhibit phase separation in their amorphous states: a pure PET phase and a mixed PAr-rich phase. In spite of this phase separation, PET crystallinity in blends, normalized to PET fraction, surprisingly goes through a maximum at 25% PAr content. The transesterfied copolymers are noncrystallizable and exhibit a single Tg between those of starting polymers, PET and PAr.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1233-1239 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Various azobenzene derivatives and polymers were attempted as materials for thin composite films containing a polymer, a liquid crystal, and lithium perchlorate which can undergo ionic-conductivity switching induced by light or heat. Poly(vinyl chloride) -based composite films containing enantiotropic azobenzene liquid crystals 1, exhibited significant ionicconductivity change based on thermo- and photoinduced phase transitions of 1, the temperature dependence on the ionic conductivity reflecting the enantiotropic phase transition behavior of the liquid crystals. Marked, reversible ionic-conductivity switching on alternating irradiation of UV and visible lights was attained with the composite films containing 1, especially 1 (n = 12). Incorporation of monotropic liquid crystals 3 to the composite films allowed bistability in the temperature dependence on the ionic conductivity. Employment of a polycarbonate resin and poly(methyl methacrylate) as the polymer material of the composite films gave similar ionic-conductivity changes to the poly(vinyl chloride) composite films, whereas polyethyleneoxide brought about some different results in the photoinduced ionic-conductivity change.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 627-635 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Preparation and characterization of novel cycloaliphatic epoxy resins, which are derived from octadienyl compounds, were studied. From a model peracetic acid epoxidation reaction using 2,7-octadienyl acetate-1, the structure of the liquid resins is estimated to be mainly terminal epoxides and some amount of inner epoxide depending on the epoxide content. The epoxy resins offer lower toxicity and lower vapor pressure. The reactivity of the resin with acid anhydrides is moderate but faster than that of traditional cyclohexane epoxide-type resins and slower than that of the glycidyl ester-type resins. This reactivity was also examined using model compounds. The heat deflection temperature of the hexahydro-phthalic anhydride-cured resins is shown to be directly proportional to the number of epoxy groups in the molecules. The flexural strength of the cured resins is nearly equivalent to that of the commercial resins, although the flexural elongation of the resins is larger than that of the rigid cyclohexane epoxide-type resins. The thermal stability of the cured resins is comparable to typical rigid cycloaliphatic resins; furthermore, high water resistance of the cured resins is suggested to be attributed to the hydrophobic character of the C8 chain by cross-linking. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 753-767 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Alumina fibers were obtained from the poly[((3-ethoxypropanoyl)oxy)aloxane] (P-3EPA) by using a polymeric precursor technology. The rheological properties of the concentrated solution of P-3EPA related to the extrusion and spinning processes have been investigated to determine the processability into fine filaments. Thirty weight percent P-3EPA dissolved into toluene showed an excellent spinnability and fine filaments of 20-30 μm in diameter were easily obtained. The phase changes during the sintering of the fiber were studied with wide-angle X-ray diffraction and were shown to be strongly related to the mechanical properties of the fiber. Further the addition of the ethyl silicate (ES) as a sintering agent which prevent the crystal growth of Al2O3 was found to be effective to improve the mechanical properties of the alumina fiber.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...