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
  • Artikel  (7)
  • Karten
  • Chemistry  (7)
  • 2020-2022
  • 1955-1959  (3)
  • 1950-1954  (4)
  • Chemie und Pharmazie  (7)
Sammlung
  • Artikel  (7)
  • Karten
Schlagwörter
Verlag/Herausgeber
Erscheinungszeitraum
Jahr
Thema
  • Chemie und Pharmazie  (7)
  • Physik  (7)
  • 1
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 11 (1953), S. 127-138 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Copolymerization studies have been made on the three two-component systems formed by the monomers methyl acrylate, 2-vinylpyridine, and dichlorostyrene, and values of the monomer reactivity ratios were determined. Terpolymers were prepared from mixtures of these same monomers, and their compositions were compared with those predicted from the kinetic data for the copolymerizations. Measurements of dissymmetry of scattered light, molecular weight, and viscosity were made on solutions in acetic acid and in methyl ethyl ketone of a terpolymer containing 37 mole per cent methyl acrylate, 47 mole per cent 2-vinylpyridine, and 16 mole per cent dichlorostyrene. The molecular weight of the terpolymer is essentially the same in the two solvents but the polymer chain is more extended in acetic acid than in methyl ethyl ketone. In nitromethane solutions of the terpolymer the ηsp/c values increase sharply with decreasing concentration. This increase is eliminated if the solutions also contain 0.01 mole per liter of a substituted quaternary ammonium iodide. These facts indicate that the polymer behaves as a polyelectrolyte in nitromethane, presumably because of reaction between the aci-form of the solvent and the vinylpyridine groups.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 554-557 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The influence of water vapor on the rate of diffusion of organic molecules has been studied at 40°C. by the sorption method for the systems water-acetone-polyvinyl acetate, water-carbon tetrachloride-polyvinyl acetate, water-acetone-cellulose acetate (37.9% acetyl) and water-benzene-polystyrene. For the first three systems the rate of diffusion of the organic vapor is markedly faster for the mixture of water and organic vapor than for the pure organic vapor. With polyvinyl acetate, the rate of diffusion of 80 mm. of acetone is increased about 25-fold if 36 mm. of water vapor is mixed with the acetone. Diffusion of the larger carbon tetrachloride molecule is accelerated by water even more than is acetone. Water vapor at a pressure of 36 mm. causes about a 30-fold increase in the rate of diffusion of 80 mm. of acetone into cellulose acetate even though the diffusion of acetone itself into cellulose acetate is anomalous. With polystyrene the presence of water vapor causes no acceleration of the diffusion of benzene which is the expected result since, in contrast to the other two polymers, polystyrene sorbs only very small amounts of water. It is concluded that the marked effect of water vapor on the diffusion of organic vapors into polyvinyl acetate and cellulose acetate involves (a) a rapid diffusion of water into the polymer and (b) more rapid diffusion of the organic vapor into the “water plasticized” polymer than into the dry polymer.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dilute solution viscosity properties of fractions of two linear and one branched sample of polyvinyl acetate in benzene and of two linear and one branched fraction in several solvents were measured at 35°C. Values of total slope, b (from plots of ηsp/c vs. c), and intrinsic viscosities were obtained under the requirement that k′ + β = 0.500 ± 0.002. Empirical plots of log b vs. log [η] gave lines which were straight within the limits of accuracy of the data. For the linear fractions in benzene, Huggins' k′ was constant and the slope of the log b vs. log [η] line was 2; for the branched fractions in benzene, k′ increased with [η] and the slope of the log b vs. log [η] line was greater than 2. The log b vs. log [η] plots form the basis for a “one-point” method for determining [η]. Consideration of these data along with results reported in the literature indicates that k′ is measurably sensitive to branching only for fractions possessing a certain minimum combination of size and complexity. However, in some cases where the variations of k′ are inconclusive, use of the slope of the log b vs. log [η] line may provide a reliable indication of branching. It was found that a comparison between the branched and linear series could also be made at constant values of [η] or b. Two linear fractions in different solvents obeyed a type of Huggins relationship in which k′ did not vary with solvent and the slope of the log b vs. log [η] line was 2. For a higher molecular weight branched fraction, however, k′ varied from solvent to solvent and the slope of the log-log plot was about 1.7. These data do not support a reference point concept of “true” intrinsic viscosity based on a simple linear relationship between b and [η]. Preliminary results dealing with the effects of the shear rate indicated that the measured viscosity properties of branched fractions may be more seriously affected by changes in shear rate than those of linear fractions.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A detailed study has been made of the rate of take-up of vapors of methylene chloride and acetone by thin films of cellulose acetate (37.9% acetyl) as a function of vapor pressure, film thickness, and temperature. It was found that the method of film preparation and conditioning greatly influenced the kinetics of the take-up. Films, which were not completely dry, exhibit a much faster rate of take-up than dry films. Dry films could he obtained by either long treatment in a vacuum oven, or by water leaching followed by vacuum drying for five days. In either case, identical kinetic results are obtained. The mercury cast films used in this work give reproducible results and show a much slower rate of take-up than a comparable glass cast film.It was found that there was no fundamental difference in the rate of take-up for the vapors of methylene chloride and acetone, although in the liquid state the former is a limited swelling agent, while the latter is a solvent. For both these yapors there is a characteristic pressure above which several anomalies appear, which make a complete quantitative explanation of the data rather difficult. The most important of these anomalies is that, if one plots the amount of vapor taken up as a function of time, an inversion of slope is observed. This inversian is very marked and is a function of film thickness. Another anomaly that appears is that the absolute amount of vapor sorbed for thinner films is greater than that for thicker films for an appreciable time interval. The effect of temperature is complex. Above the pressures where the inversion of a slope occurs, the rate is lower a t higher temperatures for a considerable range of the sorption. These effects cannot be explained on the basis of a generalized diffusion equation with the boundary conditions which have been considered so far, i.e., assuming that the outer film surface is always in equilibrium with the vapor.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Studies have been made of sorption and desorption of acetone by films of cellulose nitrate (11 and 12% N) at 30°C. by following the weight of vapor takeup or loss as a function of time. The takeup-time curves show marked inflections and plots of takeup versus \documentclass{article}\pagestyle{empty}\begin{document}$\sqrt t$\end{document} are initially nonlinear for both sorption and desorption, indicating that Fick's law with the usual boundary conditions is not obeyed. The rate of vapor takeup is also considerably more rapid and different in character for films cast on glass than for films cast on mercury. A striking result is that for successive sorption-desorption cycles the rate of sorption decreases markedly, e.g., by a factor of 16 for five cycles. Studies of the optical anisotropy of the films show that the orientation of the polymer molecules normal to the plane of the film is increased by the diffusion process and it is concluded that this accounts for the decreased rate for successive sorption-desorption cycles and provides an explanation for the diffusion anomalies. A possible cause of this orientation is the observed anisotropic swelling combined with slow movement of the polymer segments.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Studies have been made by a sorption-desorption procedure on the diffusion of water vapor at relative humidities of from 30 to 85% into the polymers, polyvinyl acetate cellulose acetate (37.9% acetyl), cellulose nitrate (12.0% N), 6-10 nylon, and polyvinyl alcohol. Diffusion of water in polyvinyl acetate obeys Fick's law at temperatures of from 30 to 50°C. and also at 22°C., which is below the second-order transition. The energy of activation for diffusion of water into polyvinyl acetate is 15 kcal. per mole and at 40°C. the diffusion coefficient is 7 × 10-6 cm.2/min. In contrast to the results with organic vapors, the diffusion coefficient for water is found to be independent of concentration of water in the polyvinyl acetate. Similar behavior is found for diffusion of water at 40° into cellulose acetate, cellulose nitrate, and 6-10 nylon. The chief difference is that for these three polymers the diffusion departs mildly from Fick's law at the later stages of some of the sorption and desorption experiments. This generally uncomplicated diffusion of water in these three polymers contrasts with the markedly anomalous diffusion found for organic vapors such as methanol and acetone into cellulose acetate and nitrate. With polyvinyl alcohol the diffusion of water is distinctly anomalous and closely resembles the non-Fickian diffusion of organic vapors in cellulose acetate and nitrate. One consequence is that the rate of sorption and desorption of water in polyvinyl alcohol is considerably slower than in the other polymers and is also concentration dependent.
    Zusätzliches Material: 7 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...