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  • 1985-1989  (13)
  • 1987  (13)
  • Polymer and Materials Science  (12)
  • Drosophila
  • Engineering General
  • Life and Medical Sciences
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 13 (1987), S. 2069-2081 
    ISSN: 1573-1561
    Keywords: Drosophila ; D. mojavensis ; D. nigrospiracula ; D. mettleri ; Diptera ; Drosophilidae ; cactus ; alkaloids ; viability ; development ; longevity ; host-plant relationships
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Drosophila mettleri is a soil-breeding, cactophilic drosophilid which lives in the Sonoran Desert. Several chemical constituents of cacti in this region have been identified as having major roles in insect-host plant relationships involvingDrosophila. For example, isoquinoline alkaloids, which are present in senita cactus, have been shown to be toxic to seven of the nine species tested. The two tolerant species areD. pachea, the normal resident, andD. mettleri. Necroses of senita cacti are often used as feeding substrates byD. mettleri adults, but this species has never been reared from senita rots. Soil, which have been soaked by juice from saguaro and cardón rots, are the typical breeding substrates of this species. The tissues of both of these cacti also contain alkaloids, chemically related to those in senita, but at much lower concentrations. Alkaloid concentration in saguaro-soaked soil was found to be 1.4–27 times the average concentration in fresh tissue. Alkaloids were extracted from saguaro tissue and used in tests of larva-to-adult viability, developmental rate, and adult longevity. Elevated concentrations of saguaro alkaloids had no significant effect on the longevity ofD. mettleri, but significantly reduced the longevity ofD. nigrospiracula andD. mojavensis, two nonsoil breeding cactophilic species. Viability and developmental rates of all three species were affected, but the effect onD. nigrospiracula was comparatively greater. It is argued that the adaptations that allowD. mettleri to utilize the saguaro soil niche also convey tolerance to alkaloids present in senita tissue. The ability to utilize senita necroses as feeding substrates represents an ecological advantage to D. mettleri, in that the density of potential feeding sites is increased as compared to species which are more specific in their host-plant relationships.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1433-1443 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of substituted phenylene-dithio-bis(phenyldithiazyl) (PDBPD) and phenylthiophenyldithiazyl (PTPD) compounds have been synthesized utilizing the facile reaction between N-trimethyl silylimides and aromatic sulfenyl chlorides. The compounds are insulators with conductivities of 10-8-10-12 (Ω cm)-1. However, they can be oxidized with Br2 to conductivities of 10-3-10-5 (Ω cm)-1 for pressed pellets. Electron donating and withdrawing substituents on the phenyl ring markedly alter the electrical transport properties. While PTPD compounds are soluble in many solvents, the PDBPD derivatives are only sparingly soluble.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2881-2892 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrogen has been found earlier to increase the initial rate of polymerization by MgCl2/EB/PC/AlEt3/TiCl4-AlEt3/MPT, CW-catalyst (+Bi, +Be) (EB, ethyl benzoate; PC, p-cresol; MPT, methyl-p-toluate), but decays more rapidly as compared to polymerizations in the absence of H2. In this study the effect of H2 was studied when either the internal Lewis base, EB Bi, or the external Lewis base, MPT Be, or both are deleted from the CW-catalyst. H2 does not affect the stereospecificity of all the catalysts, but causes a slight increase of polymer yield, whereas the yield is virtually unchanged by H2 for the catalysts activated with Be. Unlike the catalyst (+Bi, +Be) where H2 increases active site concentrations [Ti*] about threefold, it affects [Ti*] negligibly when Be is absent. The rate constants of propagation is about the same with or without H2 for the CW-catalyst (+Bi, -Be) or (-Bi, -Be); the same statement can be said about the rate constant of chain transfer with AlEt3 or with H2. Hydrogen increases the rate of catalyst site deactivation for the various catalysts in the order of(+Bi, +Be) 〉 (-Bi, -Be) 〉 (+Bi, -Be).
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2175-2183 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previous work by a number of researchers has noted the presence of anhydride during the imidization step of polyimide polymer processing from diester-diacids and diamines. This has been often, and incorrectly, dismissed as being due to the reversion of the intermediate amide-acid. Comparison of the relative rates of reactions among model compounds demonstrates the intermediacy of anhydride in the imidization reaction. When creation of the anhydride is blocked, the production of amide-acid is greatly slowed. Infrared and NMR observations of mixtures of monomers confirm the production of anhydride as a necessary intermediate in the imidization reaction occuring during the production of polyimide polymers from diester diacids.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 919-934 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Decene-l was polymerized with the MgCl2/ethylebenzoate/p-cresol/AIEt3/TiCl4-AlEt3/methyl-p-toluate catalyst at 50° using an A/T ratio of 167 and a range of monomer concentration. The concentration of the two kinds of active sites are [Ti1*] = 12% and [Ti2*] = 4% of the total titanium. The rate constants of propagation are 24 M-1 s-1. Chain transfers to AIEt3, monomer, and by β-hydride elimination have rate constant values of 1.7 × 10-3 M-1 s-1, 1.34 × 10-2 M-1 s-1, and 1.7 × 10-2 s-1, respectively. Poly(decene-l) have relatively narrow MW which are unchanged during the course of a polymerization. Therefore, the active site concentrations in the CW catalyst for propylene and decene polymerization are identical and their rate constant values agree within a factor of 2. However, the rate of decene polymerization depends on fractional order of monomer concentration and decreases with the increase of activator concentration. Furthermore, the formation of metal polymer bonds has a rate independent of these concentrations. These kinetic behaviors are a manifestation of absorption processes of these species which are not seen in propylene polymerizations.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1011-1026 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerizations of decene-1 were carried out from 0° to 70° at A/T = 167 and [M] = 0.75 M initiated by 0.17, 0.34, and 0.69 mM of Ti contained in the MgCl2/ethylbenzoate/p-cresol/AlEt3/TiCl4-AlEt3/methyl-p-toluate catalyst. The rate of polymerization is directly proportional to the catalyst concentration. About 12% of the Ti in the catalyst is initially active at 50°; they are 1.4%, 8.8%, and 9.4% at 0°, 25°, and 70°, respectively. The changes of Rp with temperature parallels the variations in the active site concentration. The decline of Rp with time has second-order plots with slopes which are inversely proportional to the catalyst concentration, but the rate constants for these deactivations are nearly the same for decene and propylene polymerizations. These results strongly support a mechanism of deactivation involving two adjacent sites in the catalyst particle surfaces. The rate constants of propagation and of chain transfer to AlEt3, the energetics for these processes, and MW and MW distribution data have been obtained.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2847-2870 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A systematic study has been made on the functions of external Lewis base (Be, methyl-p-toluate, MPT) and internal Lewis base (Bi, ethyl benzoate, EB) for the CW-catalyst system MgCI2/EB/PC/AlEt3/TiCl4-AlEt3/MPT (PC, p-cresol). Bi is a nonstereoselective modifier. It increases the active site concentrations and rate constants of propagation, kp, of both the isospecific and nonspecific sites, and thus the productivities of the stereoregular and irregular polypropylenes by five- to tenfold. It seems that Bi complexes with the MgCl2 support to lower the electronegativity of the surface Mg atoms. It also acts to lower the rate constant of chain transfer to aluminum alkyl, kAtr, by two- to fourfold. The action of Be is highly stereospecific. The isotacticity index of polypropylene is ≫ 95% in the presence of Be but ≪ 68% without it. Addition of Be decreases nonspecific [Ti*]a by about (11 ± 2)-fold; there is only about a twofold reduction of the isospecific [Ti*]i. It decreases kp,a about three times but has no effect on kp,i, so that the latter is (21 ± 4) times the former. Be decreases kAtr,i for transfer with aluminum alkyl much more than it does to kAtr,a; but it does not affect the rates of chain transfer with monomer and by β-hydride elimination or the rate of catalyst deactivation. The number of active sites without Be is [Ti*]i = 15% and [Ti*]a = 55% for a total of 70%. In the presence of Be they are both about 6%. Optimum performance in propylene polymerizations requires both Bi and Be in the case of the CW-catalyst.
    Additional Material: 14 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 945-954 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The onset of decomposition of poly(4-methyl-1,3-dioxolane) was lowered to 70°C by 0.1 wt% p-toluene sulfonic acid from 170°C in the absence of acid to produce more than 81% yield of monomer. Protonation forms cyclic oxonium ion followed by depolymerization. Minor products are isomers of hydroxymethyl-2-hydroxyl-2-methyl ethyl ether and bis(2-hydroxyl-2-methyl ethoxyl)methane from rearrangements of the oxonium ions. The first order rate constant of acidolysis of poly(4-methyl-1-1,3-dioxolane) is about 8.5 kcal mol-1, which is much smaller than about 17 kcal mol-1 for the acidolysis of poly(1,3-dioxolane).
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 57-69 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric relaxation in three segmented polyurethane-CaCO3 composites was investigated between -70°C and +150°C in the 300 Hz to 100 kHz frequency range. Two of the polymers contained a polyacetal-polyether soft segment, whereas the soft component of the third polymer was polypropylene oxide. The hard segments consisted of 4,4′-diphenyl methane diisocyanate in two cases and toluene-2,4-diisocyanate in the third case.In parallel studies two calorimetric relaxations, designated α and α′, were observed for each sample and were determined to be glass transitions of the soft and hard segments, respectively. In general, the transition temperatures decrease with increasing filler content. High frequency, low temperature permittivities increase while low frequency, high temperature AC conductivities generally decrease with increasing filler content. The shift in the transition temperatures can be explained using the adsorption theory of filler-polymer interactions and the densities of the samples. The interfacial polarization mechanism becomes important only above the α′ transition temperature and below 1 kHz.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 1459-1475 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of silicone-modified bismaleimide resins have been examined as matrices for high performance continuous fiber-reinforced composite materials. Detailed studies of the interrelation between processing, structure, and properties of both the neat resin and corresponding carbon-fiber-reinforced composite have identified that the silicone additive provides important morphological modification to the bismaleimide matrix for toughness improvements while, at the same time, retaining the elevated temperature performance. Micrographs of fracture surfaces of cured samples demonstrate remarkable similarities to fracture surfaces of rubber-modified epoxy matrices. Specifically, a fracture surface covered with noncommunicating microcavities of 1.5 μm in diameter was observed. However, unlike rubber-modified epoxies where the observed features are assumed to be created during fracture of the specimen, this study demonstrates that the microcavities are created during the cure process and, thus, exist in the bulk of the material before fracture. In simulated cures of the material either while obsered directly in a polarizing microscope or indirectly inside thermal analysis cells (DSC, TGA) and with examination of fractured surfaces of samples cured according to different temperature profiles, it is established that the silicone modifier, in conjunction with the processing conditions, is responsible for the morphological developments. Accordingly, a mechanism describing the observed morphology was proposed based on physical changes that the silicone additive experiences in relation to specific volatile products emitted during the cure process.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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