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  • 1990-1994  (71)
  • Polymer and Materials Science  (50)
  • Life and Medical Sciences  (13)
  • Organic Chemistry  (8)
  • 1
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: CH-type catalysts were prepared by reacting MgCl2 · ROH, where ROH is 2-ethyl hexanol (EH), (R)-2-octanol (R-20), and (S)-2-octanol (S-20), with TiCl4 in the presence of di-i-butyl phthalate (BP), di-i-butyl terephthalate (BT), (-)-dimenthyl phthalate (MP), or (-)-dimenthyl terephthalate (MT). The MT catalysts were found to incorporate 8.9 to 13% Ti whereas the BP catalysts contain only 1.9 to 2.6% Ti. Comparison of the CH(EH, BP) and CH(EH, MT) catalysts showed that they have about equal number of isospecific active sites per gram of catalyst and the same rate constants of propagation for their nonspecific sites, however, the isospecific sites in the latter are less active by comparison. Consequently, the CH(EH, BP) catalysts is five times more active than the CH(EH, MT) catalysts and produces polypropylene which is 97% isotactic (reflux n-heptane insoluble) as compared to 84.7% for the latter. The catalysts derived from 2-octanols are much less active than the corresponding catalysts prepared with 2-ethyl hexanol due to lack of reactivity with phthalic anhydride which permits excessive incorporation of TiCl4 to form nonstereospecific catalytic sites as well as inactive Ti species.
    Additional Material: 4 Ill.
    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 32 (1994), S. 2049-2056 
    ISSN: 0887-624X
    Keywords: metallocenes ; olefin polymerizations ; Ziegler-Natta catalysts ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Propylene was polymerized with rac-ethylene-bis (1-η5-indenyl)dichlorozirconium/methylaluminoxane in solvents of different polarity. The poly (propylene) formed was separated by solvent extraction; 13C-NMR and DSC measurements were made on the polymer fractions. The poly(propylene) in each solvent fraction has its characteristic molecular weight steric pentad distributions, melting transition temperature, and enthalpy for fusion irrespective of the polymerization medium. The results suggest that the medium dielectric constant does not affect the polymerization rate or the intrinsic stereoselectivity, propagation and chain transfer rates a given catalytic species but can alter the occurrence of steric insertion errors through shifting of distributions of the propagating species producing poly(propylenes) of different stereoregularities. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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  • 3
    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: The formation of CH-type catalysts has been investigated by high-resolution and solid-state NMR. These catalysts are prepared from a soluble MgCl2 and 2-ethyl-1-hexanol adduct (MgCl2·3EH) by reaction with phthalic anhydride (PA) to form dioctylphthalate (DOP) and then with TiCl4 in the presence of di-i-butylphthalate (BP). In the model systems MgCl2·3EH/PA, MgCl2/BP, and MgCl2/TiCl4/BP, the ester is complexed with MgCl2 and /or TiCl4 in two or more states. Only single-ester C=O and OCH2 resonances are seen in TiCl4/BP, probably due to exchange of ester coordinations. CH-catalysts prepared by three different procedures exhibit a single mode of bonding for the ester. The chemical shift values are consistent for ester complexed with MgCl2. The most active and stereoselective catalyst has the most shielded chemical shift values for the C=O and  - OCH2 -  carbons, shortest TH1 and TH1p, and longest TCH relaxation times. These parameters change monotonically with the decrease of activity and stereoselectivity of the catalyst preparation. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 479-484 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 1639-1643 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 14CH3O3H was used to quench ethylene polymerization by transition metal catalysts. 3H labeling occurred exclusively for Ti-containing catalysts, whereas more than 95% of the chains were labeled with 14CH3 for the Cr-containing catalysts. Both modes of labeling occurred with V-containing catalysts. The observed phenomena indicate a change of “coordinate-carbanionic” to “coordinate-carbocationic” character for the alkyls of Ti, V and Cr in this order.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 2579-2603 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Compounds of palladium with ten different chelated bisphosphine ligands were investigated for their catalysis of alternating copolymerization of propene with carbon monoxide. The bisphosphine structure and chelate ring size influence strongly the activity, regio- and stereo-selectivity of the catalysts. Molecular mechanics calculations on the π-olefin complex showed that the non-bonded interaction between propene and the ligands on Pd is both regio- and stereo-selective. Primary insertion is about seven times more probable than secondary insertion for the Pd complex of bis(diphenylphosphino)butane ligand. The enantioselective catalysts favor the meso enchainment of propene. Gas chromatography/mass spectrometry (GC-MS) of oligomers showed that most chains are initiated by Pd—H species with less frequent initiation by Pd—OCH3 complexes; β-hydrogen elimination is the dominant chain termination process.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A selective method using polarography was developed for the determination of the degree of adsorption of anionic polyacrylamides onto Kaolinite. Four polymers of the same anionic character but different molar mass were studied. Limiting adsorption of the polyacrylamides onto the clay increased with their molar mass.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A cationic polyacrylamide was examined using polarography, constant potential coulometry, photon correlation spectroscopy, electrocapillarity and potentiometric titrimetry. A polarographic response was found in differential-pulse polarography (DPP), direct-current and Kalousek modes at -1,7 V versus a silver/silver chloride electrode. In each case the magnitude of the response was a function of polymer concentration. However, it is thought that the response is not due to the polymer itself but impurities found with it. These were found to have a pK of 4,75. The polymer appears to develop a more open structure in LiCl solution (〈0,0013 mol/L). The unwashed polymer was found to greatly increase the interfacial tension at the mercury drop, but this effect was considerably reduced on washing the polymer in 70% acetone solution. Hydrolysis of the polymer seems to occur at pH 10. The suppression of the negative tensammetric peak of poly(ethylene glycol) (PEG200) by a range of cationic polyacrylamides was used for their analysis in the determination of their adsorption onto the surface of woodpulp. The adsorption was found to be a function of both their cationicity and mean molar mass. The rate of hemicellulose desorption from the woodpulp appears to be pH dependent. The impurity is thought to be mainly adipamic acidSystematic name: 5-carbamoylpentanoic acid..
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 1741-1748 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A technique using buffer capacity has been developed for evaluating the approximate pK values of the stability constant K, of polyelectrolytes. The technique has been applied to hemicellulose extracted from woodpulp (pK ≈ 3,9 (0,1 M NaCl)) and dextran (pK = 13,55 ± 0,2 (2 M NaCl)). Verification of the method has been obtained by applying it to acetic acid (pK = 4,55 ± 0,02 (0,1 M NaCl), pK = 4,70 ± 0,02 (0,001 M NaCl)) and glucose (pK = 12,00 ± 0,05 (2 M NaCl)). Glucose was found to turn peppermint green in NaOH solutions. At least 50% of the surface charge of woodpulp was found to originate from its hemicellulose coating.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 212 (1992), S. 257-267 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The ontogeny of various middle-ear structures was examined in 11 groups of chicks between 10 days embryonic and adult. Measurements of the tympanic membrane surface area and height, columella length, and that of the columella footplate, annular ligament, and oval window area were obtained using video micrographs and computer digitization techniques. The oval window matures first at 53 days post-hatching, whereas the columella achieves adult size at 74 days. The tympanic membrane surface area is the last middle-ear variable studied to reach adult size (79 days post-hatch). The columella increases its length from 0.63 mm (10 days embryonic) to 2.73 mm in the adult. The tympanic membrane area expands by 280% whereas the columellar footplate area increases by 11x. As a result, the pressure amplification of the middle ear due to the tympanic membrane/columellar footplate area ratio improves by over 400%. These data further contribute to our understanding of the functional development of the middle ear. © 1992 Wiley-Liss, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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