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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Analytical chemistry 36 (1964), S. 1130-1132 
    ISSN: 1520-6882
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 747-750 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The following equation for the determination of polyethylene melt strength (MS) has been derived: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm MS}({\rm poise}) = {{1.492 \times 10^7 (\Delta l)^2 r_0^2} \mathord{\left/ {\vphantom {{1.492 \times 10^7 (\Delta l)^2 r_0^2} {({\rm MF})}}} \right. \kern-\nulldelimiterspace} {({\rm MF})}} $$\end{document} where Δl is the length (inches) of extruded polymer cord required for 50% decrease in diameter of the cord, r0 is the radius (inches) of the molten polymer cord as it first emerges from the melt indexer die, and MF is melt flow rate in grams/10 min. The required measurements are made on the initially extruded 0.5-in. portion of the polymer cord from a conventional melt indexer using the standard 0.0825-in.-diameter die and 2160-g. load and a temperature of 230°C. This melt strength equation was derived by using the assumption that the melt strength can be expressed as melt viscosity at low shear rates. Melt strengths of polyethylenes having similar melt indices have been shown to have over a 37-fold difference.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 523-526 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 2 (1962), S. 164-169 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The results compare favorably with those obtained by careful refractionation of fractions isolated by the precipitation method. A convenient parameter, U, related to the breadth of the molecular weight distribution can be calculated from the slope of the log-probability plot. When the plot is linear, U, is numerically equal to the ratio Mw/Mn. Values of U obtained for a number of commercial and experimental polypropylenes indicate that, with a given type of polypropylene, the breadth of the distribution increases as the average molecular weight of the sample increases, and that wide differences in distribution can be expected from polymers made by different processes.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: It is well known that the rheological behavior of polyethylene melts is affected by at least four variables: (1) molecular weight, (2) molecular weight distribution, (3) long-chain branching and its distribution, and (4) short-chain branching. Of these, the first three appear to have the largest effects. In the present paper an attempt is made to determine the effect of molecular weight distribution by rheological studies of polymers having similar molecular weight distribution by rheological studies of polymers having similar molecular weights and degrees of branching, but varying considerably in their molecular weight distributions as determined by fractionation. The rheological parameters studied were melt recovery, non-Newtonian behavior, critical shear rate, and melt strength. It is shown that the melt recovery increases uniformly as the molecular weight distribution broadens. The degree of non-Newtonian behavior, as measured by the exponent n of the power law, also increases with distribution breadth and is particularly affected by the amount of low molecular weight polymer present. Melt strength increases in a similar manner. Critical shear rate is inversely related to the breadth of the molecular weight distribution and is particularly dependent on the molecular weight of the highest fractions. The log of the critical shear rate is inversely proportional to the melt index recovery.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Studies of the rheological properties of fractions of linear and branched polyethylenes have shown that the melt recovery of linear polyethylene fractions is very small and independent of molecular weight over a wide range. Fractions containing high degrees of long-chain branching, on the other hand, have high melt recoveries. The melt recovery of a fraction can therefore be used as an index of long-chain branching. Alternatively, if no long-chain branching is present, the melt recovery is a unique function of the molecular weight distribution. This effect is illustrated by blends of fractions. The log of the critical shear rate is a linear function of the log melt viscosity of the fraction for both linear and branched polyethylenes. This would indicate that the critical shear rate of polydisperse samples would depend primarily on the weight-average of Z-average molecular weight of the polymer. This is confirmed by previous studies on polydisperse samples. It also appears that critical shear rate is highly dependent on the homogeneity of the sample. Blends of the same fractions had quite different critical shear rates, depending on the procedure used to prepare them, even though their molecular weight distributions were identical. The change in viscosity with shear rate is not a unique function of molecular weight or melt viscosity. Fractions of linear polyethylene show a greater change in viscosity with shear rate than branched fractions of similar low shear melt viscosity. This suggests that the effect is related to chain entanglement or coordinated segmental motion.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 7
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The objective of this work was to determine the relationships among molecular and melt parameters of polyolefins. The polyolefins studied are polypropylene, poly-1-butene, poly-1-hexene, poly-1-dodecene, these have regularly spaced short-chain branches. Conclusions from previous work, as well as some new data, on polyethylene are given. As the molecular weight increases, the critical shear rate decreases but the melt viscosity and non-Newtonian ratio increase. As the molecular weight distribution broadens, the critical shear rate decreases, whereas the normal forces and the non-Newtonian ratio increase. Increasing the number of short-chain branches increases the energy of activation and the melt viscosity but decreases the non-Newtonian ratio. As the length of the short-chain branches increases, the non-Newtonian ratio increases, but the melt viscosity, critical shear rate, and energy of activation decrease. Increasing the number of long-chain branches decreases the non-Newtonian ratio, but the normal forces and the melt viscosity increase. Such information allows the polymer chemist to design a polyolefin molecule having the critical melt properties required for a given production technique.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 8
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new method has been developed for the fractionation of polyethylene, providing more reliable data on molecular weight distribution in a fraction of the time required by previous methods. The fractionation is carried out on a column of glass beads, using a combination of solvent and temperature gradients by a method similar to that used by Baker and Williams for polystyrene. The lowest temperature in the column is above the melting point of the polyethylene, so that fractionation takes place by partition of the polymer molecules between two liquid phases in transient equilibrium. Because of the combined solvent and temperature gradients, the polymer is transferred from the stationary to the moving phase many times in its passage down the column; consequently, the fractions are considerably narrower than those obtained from a single-step fractionation. A simple apparatus which will fractionate up to 5 g. of polyethylene in a 24-hr. period is described. The effect of such experimental variables as column load, solvent flow rate, and the type of solvent gradient was determined. Experimental data obtained on several commercial polyethylenes are given.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 215-226 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The influence of preparative conditions on the molecular weight and stereoregularity distributions of polypropylene was investigated. The stereoregularity distribution is narrowed by using a highly stereospecific catalyst, by decreasing the polymerization temperature, and for the three-component catalyst by keeping the mole proportion of the electron-donating third component at 0.5. The molecular weight distribution can be narrowed by using a highly stereospecific catalyst, a high monomer concentration, and a high polymerization temperature, and by having a lower conversion, particularly at low monomer concentration. The possibility of long-chain branching in polypropylene was indicated by data from the fractionation of tritium-labeled polymers.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 10
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Copolymerization of propylene and 1-butene with highly stereospecific three-component coordination catalysts produced multiblock crystalline copolymers having stereo-regular sequences of both propylene and 1-butene. Copolymers containing from 3 to about 80% 1-butene had two DTA melting points which were attributable to polypropylene and poly-1-butene crystallinity. Those containing from 18 to about 70% 1-butene had x-ray diffraction patterns showing peaks characteristic of polypropylene and form I poly-1-butene, but form II poly-1-butene crystallinity was never observed. The multiblock copolymer structure observed is also supported by the fact that the product of the reactivity ratios is greater than unity. The composition distributions of low-conversion and continuously prepared copolymers were similar and relatively broad. For example, copolymers containing an average of 12% 1-butene had species containing from 5-30% 1-butene. High-conversion copolymers had an even broader composition distribution due to the gradual increase of the 1-butene concentration in the comonomer mixture as the copolymerization proceeded. The absence of homopolymers was demonstrated by fractionation. The ability to detect homopolymers was proved by the fact that a mixture of stereoregular polypropylene and poly-1-butene were readily separated. Increasing the amount of 1-butene tended to decrease those properties dependent upon crystallinity such as hardness, tensile strength, stiffness, density, and melting point, but tended to improve significantly the impact strength, low temperature properties, and clarity of molded objects. These duocrystalline copolymers retained a much higher level of properties than that observed for random copolymers prepared with less stereospecific coordination catalysts.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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