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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 10 (1996), S. 733-740 
    ISSN: 0268-2605
    Keywords: arsenic speciation ; seasonal change ; methylarsenical ; seawater ; sediment ; biological activity ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The distribution of arsenic species, including trivalent methylarsenicals, was observed in coastal seawater of Tosa Bay and Uranouchi Inlet Japan. In Tosa Bay, most arsenic was dissolved in the inorganic form throughout the year and the concentration of total dissolved arsenic was higher than that in Uranouchi Inlet. The sum of methylarsenicals found in surface waters comprised 2-25% and 10-82% of the total dissolved arsenic in Tosa Bay and Uranouchi Inlet, respectively. In Uranouchi Inlet, seasonal variations in the concentrations of arsenicals were observed both in the water column and in surface sediments. The maximum concentrations of methylarsenicals appeared during summer, and became comparable to those of inorganic arsenicals in surface water. The concentration of trivalent methylarsenicals was usually low, and their seasonal changes seemed to be independent of those of the pentavalent species. The variations in methylarsenic(V) concentration did not coincide with those of chlorophyll a in either Tosa Bay or Uranouchi Inlet. These results suggested that methylarsenic(V) in natural waters was produced not directly by the activity of phytoplankton but through decomposition of organic matter by bacteria.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 305-311 
    ISSN: 0268-2605
    Keywords: arsenic speciation ; seasonal change ; arsenic methylation ; redox conditions ; freshwater ; hypolimnion ; biological activity ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Seasonal changes in the distribution of arsenic species were observed in a dredged area in the southern basin of Lake Biwa, Japan. The concentrations of dimethylarsenic acid [DMAA(V)] became comparable with those of inorganic forms during a stratification period. DMAA(V) increased not only in the photic zone but also in the hypolimnion. In the photic zone, an increase in DMAA(V) was observed with the yearly maximum of water temperature. In the hypolimnion, the seasonal changes in methylarsenicals differed from those in surface waters. DMAA(V) maxima appeared seasonally under sub-anoxic conditions and developed regionally at the redox boundary and above the sediment surface. The DMAA(V) concentrations increased in the initial period of oxygen depletion and just after the disappearance of anoxia, while they diminished in the anoxic hypolimnion by midsummer. The seasonal behavior of trivalent methylarsenicals, which are readily oxidized in oxic environments, was similar to that of DMAA(V). The total arsenic concentration in the surface layer rose to a maximum in late summer. Methylarsenicals did not increase in such a way that the total arsenic concentration increased during summer. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 241-251 
    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 reaction of isobutene (IB) with its dimers (IB2) catalyzed by CF3SO3H yielded isobutene trimers (IB3) in high yield in nonpolar solvents at 0°C. The initial feed of isobutene, in the presence of equimolar IB2 or more, was selectively converted into IB3 without loss or accumulation of IB2. After complete consumption of the isobutene, however, the remaining IB2 rapidly dimerized to isobutene tetramers (IB4). 13C-NMR analysis of the products showed that the IB3 was formed via addition of the t-butyl cation (protonated isobutene to 2,4,4-trimethyl-1-pentene (an IB2 isomer); the trimer fraction was free from isomers arising from addition of the t-butyl cation to 2,4,4-trimethyl-2-pentene (another IB2 isomer) or addition of the IB2 cation to isobutene. The IB3 thus obtained was further oligomerized with CF3SO3H catalyst in nonpolar media in the range of 0 to -25°C to give a mixture of IB5, IB6, and IB7 in high yield. With EtAlCl2 as catalyst, reaction of isobutene with IB2 and oligomerization of IB3 both resulted in products with a broad molecular weight distribution containing higher oligomers and complex hydrocarbons formed via cracking of the intermediate carbocations.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 2593-2603 
    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: Lower oligomers (dimer to tetramer) of 1-hexene were obtained in high yield (65 wt %) with a new cationic complex catalyst, EtAlCl2—CCl3CO2H, in n-hexane at 70°C, trimer being the major product. A strong oxo acid, CF3SO3H, yielded very similar products under the same conditions. Characteristics of the 1-hexene oligomerization by these two catalysts were the high selectivity for dimers to tetramers and the absence of cracking of the product. In contrast, EtAlCl2 or AlCl3 alone led to oligomers with a higher molecular weight (∼103) and a broad molecular weight distribution, the structure of which was very complicated because of extensive cracking of products. A series of EtAlCl2—chloroacetic acid (CClnH3-nCO2H, n = 0-3) complexes were also examined as catalysts. The yield of dimer to tetramer increased with increasing acidity of the chloroacetic acids. The mechanism of the 1-hexene oligomerization with these complex catalysts was discussed on the basis of the structure of product oligomers.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 171-181 
    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: Isobutylene tetramers (IB4) were obtained in high yield by the cationic dimerization of commercial diisobutylene (DIB) (2,4,4-trimethyl-1-pentene with isomeric impurities) with CF3SO3O3H or CH3COClO4 as catalyst. The best IB4 yields (80-90%) were achieved at 0-30°C in nonpolar solvents (n-hexane and CCl4). The major components in the IB4 produced under these conditions were 2,2,6,6,8,8-hexamethyl-4-methylenenonane (8) and 2,2,4,6,6,8,8-heptamethyl-4-nonene (9) that arose via simple linear dimerization of DIB. The yield of IB4 was almost independent of the monomer concentration ranging from 10 to 50 vol % at 0°C, but decreased at higher temperatures (〉50°C) or in a polar solvent [(CH2Cl)2] because of the formation of higher oligomers and side reactions such as cracking. A Lewis acid catalyst (AlEtCl2) resulted in a very complex mixture of C12-C20 hydrocarbons at 0°C in CCl4; the yield of IB4 was less than 40%. The catalytic difference between oxo acids and metal halides is discussed.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2025-2037 
    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: An investigation has been made into the effect of mixing by a screw extruder upon the molecular characteristics and the melt flow properties of high-density polyethylene. The crosslinking between molecules predominates over the scission of a molecule at an early stage of mixing, but with further increase in the degree of mixing, this situation reverses itself to bring about the formation of branched polymers. Static flow and dynamic viscoelastic properties of molten high-density polyethylene change considerably with increase in the degree of mixing. The apparent viscosity drops rather sharply after mixing. The dynamic properties for the original resin show smaller frequency dependence of the viscosity and larger dependence of the rigidity than those for extrudates. The relaxation spectra become broader with increase in mixing. These may mainly be due to the change of the molecular characteristics of high-density polyethylene with mixing by an extruder.
    Additional Material: 12 Ill.
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