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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 16 (1955), S. 549-576 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization in solution of a variety of water-soluble monomers with a variety of water-soluble redox initiators is described and a detailed study is reported on the polymerization, in aqueous solution, of methyl vinyl ketone and of methyl methacrylate under the influence of potassium sulfate-silver nitrate. Keeping the persulfate concentration constant and varying the silver nitrate or, conversely, keeping the silver nitrate constant and varying the persulfate, it is found that, except at very high concentration of catalyst, both the rate of polymerization and the molecular weight of the polymer bear a linear relation to the square root of the catalyst concentration, in harmony with the general theory of catalyzed bulk and emulsion polymerization. The molecular weight of the polymer formed diminishes with increase in the temperature of polymerization. The study of redox polymerization in water, without emulsifier, has been extended to the case of a mixture of a water-soluble and a water-insoluble monomer, and it has been found that copolymerization proceeds at a reasonable rate and frequently forms a stable latex. The copolymerization of styrene and 5 or 10 per cent of its weight of methacrylonitrile in water under the influence of a water-soluble persulfate-bisulfite redox pair has been examined with some closeness. Polymerization is apparently initiated in the aqueous solution, since, contrary to the state of affairs in emulsion polymerization, water-soluble retarders are more effective than oil-soluble ones, when the retarder is added at the outset. If the retarder is added at a later stage of polymerization, oil-soluble reagents are more effective than water-soluble ones. The water-soluble monomer enters into the polymer at a greater rate than the water-insoluble one, but it appears that, even at the earliest stage at which it is practicable to take samples co-polymerization occurs. The influence of catalyst concentration on the rate of polymerization, the molecular weight of the polymer, and the latex particle size was examined.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Biochemical and Microbiological Technology and Engineering 1 (1959), S. 59-76 
    ISSN: 0368-1467
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An apparatus is described in which large numbers of algal cultures can be maintained under the following conditions: (1) Constant temperature within the range 5 to 70°C, four different temperatures being maintained simultaneously; (2) uniform illumination at intensities up to 20,000 metre-candles; (3) continuous shaking at variable speed; and (4) aeration under aseptic conditions with mixtures of up to four different gases in any desired proportions.Among other features, thermoregulator heads, flow-meters and heaters for sterile filters, of improved design are described.To illustrate the use of the apparatus, data showing the effects of light intensity and temperature on the growth of Monodus subterraneus are presented.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2017-09-01
    Description: Copper ions exchanged into zeolites are active for the selective catalytic reduction (SCR) of nitrogen oxides (NO x ) with ammonia (NH 3 ), but the low-temperature rate dependence on copper (Cu) volumetric density is inconsistent with reaction at single sites. We combine steady-state and transient kinetic measurements, x-ray absorption spectroscopy, and first-principles calculations to demonstrate that under reaction conditions, mobilized Cu ions can travel through zeolite windows and form transient ion pairs that participate in an oxygen (O 2 )–mediated Cu I -〉Cu II redox step integral to SCR. Electrostatic tethering to framework aluminum centers limits the volume that each ion can explore and thus its capacity to form an ion pair. The dynamic, reversible formation of multinuclear sites from mobilized single atoms represents a distinct phenomenon that falls outside the conventional boundaries of a heterogeneous or homogeneous catalyst.
    Keywords: Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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