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  • Analytical Chemistry and Spectroscopy  (963)
  • Physics  (889)
  • 2010-2014
  • 1980-1984  (1,454)
  • 1965-1969  (398)
  • 1925-1929
  • 1981  (1,454)
  • 1966  (398)
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  • 2010-2014
  • 1980-1984  (1,454)
  • 1965-1969  (398)
  • 1925-1929
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 659-662 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of the α polymorph of nylon 4 has been determined from the x-ray diffraction patterns of uniaxially oriented monofilaments. In general the crystal structure of α nylon 4 is similar to that of α nylon 6. The unit cell is monoclinic with the following dimensions: a = 9.29 ± 0.05 A., b = 12.24 ± 0.05 A., c = 7.97 ± 0.05 A., and β = 114.5 ± 1.0°. There are eight monomeric units in the unit cell. The theoretical density is 1.37 g./cc. and the observed density 1.25 g./cc. The space group is P21. The nylon 4 chains are of the extended planar zigzag type, with the plane of the zigzag approximately parallel to the a axis of the unit cell. Along the a axis, every other chain is inverted - an antiparallel arrangement of chains - thus permitting complete hydrogen bonding and the formation of sheets of nylon 4 chains. Along the c axis of the unit cell, the second sheet is displaced by3/10 of the b axis, thus leading to a staggered arrangement of sheets. The sheets are held in place by van der Waals forces.
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  • 3
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 599-610 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is described for the conversion of polystyrene to poly(styrenesulfonic acid) without change in the molecular weight distribution; the reaction is performed at room temperature in 100% H2SO4 and uses Ag+ catalyst. The resulting polyelectrolyte has solubility and other characteristics significantly different from those of previously investigated poly(vinylsulfonic acid). This permits a study of the influence of the aromatic group on the local and long range interactions in solution. The barium salt of poly(styrenesulfonic acid) is unusual in showing both upper and lower consolute temperatures in solution.
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  • 4
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 611-629 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Epitaxial deposition of homopolymers from solution [polyethylene, isotactic polystyrene, poly-3,3-bischloromethyloxacyclobutane (Penton) and polypropylene] was found on the (001) faces of cleaved alkali halide single crystals. Electron and optical microscopy studies have shown that the polymer usually grew from small, rodlike crystallites which were oriented in (110) directions of the halide crystal. Large oriented, four-leaved, “rose” structures also were observed for polyethylene. Electron diffraction studies indicate that the polymer chain axes for polyethylene, isotactic polystyrene, and Penton generally lie parallel to the (001) faces of the halide crystal and are also oriented in the 〈110〉 directions of the crystal face. Investigations on the effect of various halide substrates upon the epitaxial crystallization habit of polyethylene inferes that lattice matching does not play the major role in orientation. Two possible explanations are offered for this epitaxial behavior.
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  • 5
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 631-638 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of basic aluminium dibenzoate upon the supercooling of polypropylene fractions of molecular weight 9.2 × 103-1.25 × 106 was determined by differential thermal analysis. The response to heterogeneous nucleation within the precision of the method used appears to be only slightly dependent, if at all, upon the molecular weight of the polymer.
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  • 6
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 639-647 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wideline NMR techniques have been applied to both singly and doubly oriented specimens of nylon 66. Variations in the spectra obtained are observed for different orientations of the specimens relative to the applied field. These variations demonstrate that the zigzag chain axis is essentially parallel to the draw direction and that motion occurs in all of the sample. The motion is of two types: random in the mobile regions and rotation of segments about the chain axis in the rigid regions.
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  • 7
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 663-665 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 8
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 649-657 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization kinetics of poly(n-octadecyl methacrylate) has been studied at the air-water interface. The rate of the crystallization has been measured by the decrease in the area of monolayers with time at various temperatures and surface pressures. The crystallization isotherms have been analyzed by the general mathematical treatment of the kinetics of phase changes, and the results show linear growth to be dominant. The variation of the rate constant with temperature and pressure has been illustrated by the difference in the supersaturation defined by introducing the equilibrium pressure-area isotherms.
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  • 9
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 668-672 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 10
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    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 673-684 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Specific heats of plasticized poly(vinyl chloride) can be readily obtained by means of the thin foil calorimeter when the polymer is fabricated into sheet or film. The effects of temperature and plasticizer content on the specific heat and of the plasticizer content on the glass temperature are readily observed. The data may be used to estimate the glass temperatures of plasticizers where those temperatures are not readily reached by normal techniques. The specific heat at the glass temperature is approximately 0.255 for the ranges of 0-30 phr plasticizer. A definite glass transition is not observed with 60 phr plasticizer. No other transitions were observed between 200 and 400°K. The previous history of the polymer is important, as it can change the specific heat of the polymer noticeably, especially above the glass temperature. Comparison of the values listed here with those obtained by others should be made with the understanding that these samples were fabricated by extrusion and were free of observable strain. The degree of crystallinity of these polymers is very small, probably less than 10%, since none was found by x-ray diffraction. The plasticizing effect of some stabilizers was noted.
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  • 11
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 697-704 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Depolarization currents were used to study the persistent polarization induced in polystyrene and poly(methyl methacrylate) by cooling with flow under pressure. These studies showed that the charge on electrets made by flow under pressure consists in part of a surface charge which leaks off rapidly in moist air and in part of a charge due to volume polarization which decays more slowly. The volume polymerization produced in poly(methyl methacrylate) by flow under pressure is of the same order as that produced by cooling under a voltage drop, but flow under pressure produces a larger surface charge.
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  • 12
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ability of various polymers to acquire persistent polarization (i.e., to become electrets) was investigated. Polarization was induced in the polymers by two methods: (a) by cooling under a voltage drop and (b) by cooling with flow under pressure. There was found to be an optimum temperature for electret formation by either method. This optimum temperature was roughly 37°C. above Tg when polarization was produced by application of a voltage drop and roughly 57°C. when polarization was produced by flow under pressure. Crystallinity and the nonhomogeneities present in blended polymers were harmful to electret formation, but a small critical amount of ionic impurity was helpful.
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  • 13
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 705-714 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The determinations of the number-average molecular weight of polyethylene by cryoscopy has been improved, permitting precise measurements with both linear and branched polyethylenes in the molecular weight range 4,000-30,000. Improvements include a cryometer of new design, a lower-melting cryoscopic solvent containing a nucleating agent to control supercooling and rate of crystallization of the solvent, and more precise measurement of freezing point depression. Polyethylene samples are dissolved in hexamethylbenzene admixed with 0.1% of cadmium iodide, and steady-state freezingpoint depressions are measured with a thermistor to a maximum sensitivity of 5 × 10-5°C. Molecular weight measurements are reproducible to within ±10%. The cryoscopic apparatus and procedure are described in detail, and results obtained with samples of linear and branched polyethylene are presented and discussed.
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  • 14
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 765-775 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The behavior of films of polyelectrolytes at the water-organic liquid interface depends on the nature of the interface and the pH of the substratum. The present paper investigates the influence of these two factors on the cohesive forces between monomer units. Two polyelectrolytes were studied: poly(methacrylic acid) (APM) and poly-2-vinylpyridine (2-PVP). In the case of uncharged films, the collapse pressure decreases when the polarity of the organic phase becomes more important, whereas the term ω/kT, which appears in the theory of Motomura and Matuura, increases. A quantitative relation between the parameter ω/kT and the collapse pressure may be deduced. The behavior of the ionized surface film at different pH values is modified by the choice of the interface. However, there exists a competition between two phenomena: the dissolution of ionized residues in the substratum and the electrostatic repulsion between charges in the surface plane. Depending upon whether the first or the second parameter is more important, we observed that the surface pressure decreased or increased with the degree of ionization.
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  • 15
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 731-743 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Gel permeation chromatography is an elution chromatographic process depending on the permeation of the solute through a bed of gel particles. This process is used in the estimation of molecular weight distributions of polymers, since elution occurs in decreasing order of molecular size. The eluting species, however, are not perfectly fractionated, and apparent broadening of the distribution occurs. This broadening results from an axial (longitudinal) mixing of the eluting species. Consideration of the accessible bed volume for each species permits a correction to be made for this axial dispersion. The concept was applied to heterodisperse distributions by solving the resulting simultaneous equations. A least-squares regression may be employed to utilize the experimental data most effectively. The experimental chromatogram can be described in terms of accessible bed volume and dispersion coefficient of each species together with flow rate, sample concentration, and chromatograph column geometry. The chromatogram corrected for the axial dispersion describes the molecular weight distribution more accurately than does the experimentally determined curve. The correction procedure was applied to a well-characterized polystyrene; the results of the gel permeation chromatography show excellent confirmation of the results of fractionation and of other instrumental analyses.
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  • 16
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Torsional creep measurements on four natural rubber vulcanizates, crosslinked to different degrees, were carried out in the temperature range from -50 to 90°C. This investigation complements the studies on identical samples of the stress relaxation behavior by Chasset and Thirion and of the dynamic mechanical response by Ferry, Mancke, Maekawa, Ōyanagi, and Dickie. The creep measurements reported are shown to be in agreement with the stress relaxation results. In addition to the usual temperature reduction, a superposed curve was obtained for the long time response using the apparent molecular weight between crosslinks, Mc, as a reduction variable. The variation in viscoelastic response with crosslink density is interpreted as a restrictive action of the chemical crosslinks on the transient entanglement network.
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  • 17
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization kinetics of crystalline fractions of propylene oxide polymers made with different catalysts have been studied by isothermal dilatometric and microscopical measurements. Isothermal microscopical measurements indicate that spherulite growth in these polymers proceeds from predetermined nuclei. The half time for spherulitic appearance is less than, but of the same order as, the half time for complete crystallization. Only by taking this factor into account can the dilatometric data be represented by the Avrami equation. The deviation of the crystallization isotherm from that predicted from the microscopical data using the Avrami theory is attributed to a secondary crystallization process taking place within the spherulite. Crystallization continues long after spherulites completely occupy the available volume in the polymer. By assuming that the secondary crystallization proceeds as a first-order process in the uncrystallized, but crystallizable, portions of the melt, it is shown that the crystallization isotherms can be completely described in terms of four parameters. These are: (1) the time constant for the primary crystallization process; (2) the time constant for nucleation; (3) the time constant for the secondary crystallization process, and (4) the extent of secondary crystallization. The important conclusions of these studies are: the rates of nucleation and of spherulitic growth are far more dependent on temperature than on stereoregularity; the ratio of the rate of the secondary crystallization process to that of the primary crystallization process is almost independent of temperature, but increases with increasing stereoregularity of the polymer.
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  • 18
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 777-788 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of polypropylene crystallized at pressures up to 5000 atm. has been studied. Upon slow cooling from the melt at 320 atm., the γ modification, previously found only in low molecular weight and stereoblock fractions, begins to appear in small amounts in addition to the normal α monoclinic form. As the pressure is increased further, a larger proportion of the sample crystallizes in the γ form until, at 5000 atm., only the γ modification is present. X-ray and DTA studies show that the γ form of polypropylene transforms to the normal α modification at a temperature only slightly below the γ melting point. Evidence is presented which favors the occurrence of a solid-state transition as a model of transformation to the α form. Results from isothermal crystallizations at low supercoolings and annealing experiments under high pressure show that the melting point of the γ modification of polypropylene is very sensitive to crystallite perfection.
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  • 19
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 817-825 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The vapor pressure osmometry method for determining the molecular weight of polyamides has been studied by use of the newly developed solvents. Polymers used were polycaprolactams, polyenanthamides, and polypelargonamides. The measurements were carried out with 2,2,3,3-tetrafluoro-1-propanol and 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoro-1-heptanol as solvents at 50 and 130°C., respectively. Endgroup determinations on samples were also done in m-cresol by 0.1 N-hydrochloric acid. Reduced resistance differences (ΔR/C)0 obtained by vapor pressure osmometry at 50°C. were found to be in linear relation with the reciprocal of the number-average molecular weight determined by endgroup titrations; but anomalous results were obtained when dodecafluoroheptanol was used as the solvent at 130°C.
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  • 20
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 797-816 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The orientation behavior of stereoregular poly(vinyl alcohols) was investigated during stretching and after releasing the stress on the bulk polymers at relatively high humidity (80% R. H.) A structural model, differing from polyethylene, was proposed in which the crystallites were embedded in a considerably swollen amorphous matrix without any definite physical interaction so as to form an aggregation of crystallites, a superstructure. The crystal orientation followed, in principle, “the first borderline case” of Kratky, but with some difference from theory in orientation, while the noncrystalline orientation was represented by the freely jointed equivalent chain model of Kuhn and Grün with a value of N/γ as small as around 5. The difference between crystal orientation found and the theorietical orientation is discussed and some factors which prevented the crystal orientation are considered.
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  • 21
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 789-796 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mechanical damping measurements were carried out in the range of 103-105 cps and between 60°K. and the softening point on some substituted Polystyrenes and poly(vinyl benzoates) containing different substituents (methyl groups, methoxy groups, and halogen atoms) either in the ring or in the main chain. The ortho and meta ring-substituted polystyrenes do not show any secondary mechanical relaxation in the glassy state, although all the other substituted polystyrenes, exhibit a low-temperature damping peak (δ process) (which is in some way connected with ring motions) whose height and temperature location depend on nature, position, and number of substituents. Substituents in the para position of the ring or in the α position in the backbone chain shift the δ peak of the unsubstituted polystyrene towards higher temperatures; this shift is accompanied by an increase of the apparent activation energy E*. Substitution in the β position, on the contrary, does not affect the δ peak. Analogous results are obtained for substituted poly(vinyl benzoates), which exhibit, in addition, a β relaxation effect, associated with carboxyl group motions. A very good correlation is found between the values of E* and the limiting relaxation time τ for the δ relaxation of polystyrenes and poly(vinyl benzoates), similarly substituted in the ring, indicating that the δ relaxation leads to absorption curves in the mechanical relaxation spectrum which are characteristic of the structure of the aromatic side chain.
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  • 22
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 827-829 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 23
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 830-831 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 24
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 835-844 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The second virial coefficients of amylose acetate fractions have been determined at different temperatures and have been analyzed according to recent theories of second virial coefficient.
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  • 25
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 845-854 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic viscoelastic properties of 10 and 20% aqueous solutions of sodium polyacrylate were studied by the electromagnetic transducer method at 500 cps in the temperature range of 0-50°C. These solutions distinctly showed a relaxation phenomenon in this temperature range which was also affected by addition of such compounds as sodium chloride, urea, and dioxane. An anomalous behavior that cannot be explained as due to the relaxation phenomenon was observed on the addition of small amounts of these agents. One of the causes of this behavior is ascribed to the ion association in the solution. The static viscosity of the solution was also measured by using a rotating cylinder viscometer and the results compared with the dynamic data.
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  • 26
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 855-868 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transitions of an ionic polymer in bulk have been studied as a function of the counterion for various homo- and copolymers. It is shown that the glass transition temperature can vary by as much as 530°C., from -10°C. for the nonionic material to +520 for Ca2+ or Zn2+ substituted polymer. From simple electrostatic considerations, it is shown that a linear correlation should exist beween the glass transition and the ratio of the cation charge, q, to the internuclear distance, a, between cation and chain anion; for this particular material (the polyphosphate chain) the relation is Tg = 625(q/a) -12 where q is in units of one electron and a is in A. If the data are interpreted in the light of the Gibbs-DiMarzio theory, it is seen that both the chain stiffness and the intermolecular energy increase in an approximately parallel manner as q/a increases.
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  • 27
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 869-880 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The configurational entropy of the polyethylene chain at the melting points calculated in two ways. In both calculations, tetrahedral angles and discrete trans and gauche arrangements of all bonds are assumed, and trans bonds are assumed more stable than gauche by energy U1. First, calculations are made on chains of up to N = 18 bonds, disallowing all configurations having overlapping atoms, and the result is extrapolated to large N. Second, a calculation is made directly for long chains, with overlaps excluded only over every short chain segment. The results are in almost exact agreement, suggesting that the second method can be safely used with other molecules. The calculated configurational entropy is in line with that suggested by the entropy of fusion, assuming the chains to acquire a configurational freedom in the melt which approaches that of independent chains.
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  • 28
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 881-897 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The angular distribution function P(θ) for intensity of light scattered by a dilute solution of comblike branched molecules has been determined for three situations of some interest for evaluation of experimental data: (1) the molecules are identical with branches of equal length attached equidistantly along linear backbone chains; (2) the molecules are homogeneous in mass, with the same number of branches on each molecule, but the branches are distributed at random along the chain; (3) branches and main chains are still uniform, but the molecules are heterogeneous in mass with the number of branches per molecule distributed according to the binomial distribution and the branches in any molecule spaced randomly along the backbone. Examination of numerical results shows that the scattering functions for models (1) and (2) are not very different. The function for case (3) is somewhat different from the others when the mean number of branches per molecule is small but they contain a large fraction of the mass of the molecule. Over a limited range of the pertinent variables (corresponding roughly to observations on typical vinyl polymers of molecular weights up to 106) all three functions agree quite well with P(θ) for homogeneous linear chains with the same mean-square radius of gyration.
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  • 29
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 923-942 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A light-scattering study is presented of two isotactic polypropylene samples with broad molecular weight distributions (Mw/Mn = 8.1 and 8.7, respectively) dissolved in α-chloronaphthalene at 147°C. Incident radiation of 5460, 4358, and 3650 A. was used. The reciprocal intramolecular scattering function, P-1(u) is expressed as a function of the variable [sin(θ/2)/λ′]2. This provides a wider range of experimental values of the variable u = 16π2(b2/6) [sin(θ/2)/λ′]2 than is accessible by the usual technique of using only one wavelength. The shape of the function P-1(u) is closer to that predicted theoretically if the weight distribution function f(N) in the equation \documentclass{article}\pagestyle{empty}\begin{document}$ P(u) = \int_0^\infty {Nf(N)P_N (u)dN} /\int_0^\infty {Nf(N)dN} $\end{document} is given by the log-normal distribution rather than the distribution function of Schulz and Zimm. The method is applicable to polymer samples for which the average molecular weights are too low to be measured by the light-scattering method of Benoit and Loucheux.
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 571-586 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The changes in x-ray orientation brought about by the treatment of cotton and ramie with caustic soda of different concentrations have been studied. With ramie the effect of the treatment is to decrease the x-ray orientation, while with cotton the reverse is true. The cause of this difference is traced to a difference in the morphology of the two fibers rather than a difference in their fine structure.
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 559-569 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical properties of poly-4-methylpentene-1 have been measured in torsion in the temperature range from 25 to 160°C. at frequencies from 10-3 to 10 cps. Two transitions are found. The first, with a peak at 40°C. at 1 cps, appears as a normal glass transition. A broad high temperature peak appears at 130°C. The dynamic compliance-frequency data can be superposed by the conventional method of reduced variables for temperatures up to 100°C. The temperature dependence of the shift factors follows the WLF equation. Above this temperature, superposition can be achieved by applying horizontal and vertical shifts to both components of the dynamic compliance. When the vertical shift is permitted, the range of applicability of the WLF equation is extended to 160°C.
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 545-557 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two sets of dynamic mechanical property data and some stress relaxation data for semicrystalline, linear polyethylene are treated by data reduction methods previously described. These data can be represented by a master plot of reduced modulus versus reduced frequency and two sets of temperature-dependent shift factors. The first of these factors reflects the change of viscoelastic relaxation times with temperature. The second represents a separable change of modulus with temperature which applies over the entire time or frequency range of the experiments. This change is larger and in the opposite direction to that found applicable in the behavior of noncrystalline plastics and rubbers. The two sets of dynamic data show the same frequency-temperature dependence which can be represented by an activation energy of 22 kcal./mole. Small differences in the modulus-temperature dependence are attributed to differences in molecular weight or annealing conditions. The stress relaxation data superposes to a curve in good agreement with the dynamic data but with a factor of 20 difference in time scale. This difference is attributed to the finite strains used in the stress relaxation measurements. Such strains might be expected to increase free volume in simple extension deformations and so accelerate the relaxation.
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    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 587-598 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: NMR measurements on undrawn polyethylene (PE) samples in contact with a solvent such as C2Cl4 indicate an increase in the mobility of the mobile chain segments as compared to dry samples. Highly drawn PE shows no such effect. This is because Sa, the sorption per unit mass of noncrystalline material present, decreases from 20.9 wt.-% (dry basis), found for undrawn quenched PE, to 0.63 wt.-% after drawing (Sa determined at 25°C. and 0.80 vapor activity). Drawing also reduces the segment mobility according to the NMR spectrum. It is shown that these effects are caused by considerable structural changes occurring in the noncrystalline regions of PE upon drawing. Annealing of drawn PE samples at successively higher temperatures leads to a gradual relaxation of the noncrystalline regions towards the state characteristic of undrawn PE. With increasing annealing temperature Sa as well as the mobility approach values found with undrawn PE.
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    Journal of High Resolution Chromatography 4 (1981), S. 11-16 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; SCOT column ; Coating, liquid phase ; Single-step coating ; Phenols ; Phenolic acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A single-step coating method for the preparation of glass capillary SCOT columns is described. It is reproducible and less time-consuming than the well-known two-step coating procedures. Other methods attempted are discussed briefly. Both the flame ionization and electron capture detectors could be used in conjunction with temperature programming. The separations achieved with an “activity mixture”, phenols and phenolic acids, illustrate the resolution obtained. The columns are suitable for quantitative determinations and a comparison is made with a conventional packed column.
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    Journal of High Resolution Chromatography 4 (1981), S. 35-36 
    ISSN: 0935-6304
    Keywords: Gel permeation chromatography, GPC ; High-speed analysis ; Pollen allergen extract ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 115-120 
    ISSN: 0935-6304
    Keywords: TLC ; Gradient and continuous development ; Amino acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thin-layer gradient elution chromatography is a convenient technique for separation of very complicated mixtures; in some cases the gradient technique can be replaced by continuous development. The two techniques are compared in practice by using them to separate a mixture of dabsyl derivatives of amino acids.
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    Journal of High Resolution Chromatography 4 (1981), S. 123-124 
    ISSN: 0935-6304
    Keywords: (GC)2 in short capillaries ; Liquid crystalline stationary phase ; Supercooled temperature range ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 302-304 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Hemagglutinin glycoprotein of influenza virus investigated ; Peptide separation ; 14C labeling for identification ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The potential of reverse-phase high-performance liquid chromatography (RP-HPLC) for the separation of the tryptic glycopeptides of the hemagglutinin (HA) glycoprotein of influenza virus has been investigated. Excellent separation was accomplished with sample recovery of at least 90-95% by the utilization of an octadecasilyl silica stationary phase and a phosphoric acid/n-propanol solvent system. Eight glycosylated tryptic peptide classes were resolved from the HA glycoprotein of the A/USSR/90/77 virus strain.
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    Journal of High Resolution Chromatography 4 (1981), S. 477-478 
    ISSN: 0935-6304
    Keywords: Square relationship ; Effect of separation efficiency ; Simple equation for plate comparison ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 42-42 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 141-142 
    ISSN: 0935-6304
    Keywords: TLC ; Reflectance ; Transmission ; Probability vector ; Transition matrix ; Markov chains ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Changes of reflected and transmitted light in cases where a band lies in different sublayers of a thin-layer chromatogram are calculated by the use of Markov chains. The problem of a “random walk with absorbing barriers” is described and compared with the problem of transmission and reflectance of light in a layer of sorbent.
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    Journal of High Resolution Chromatography 4 (1981), S. 151-155 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; XAD-2 resin ; Fungicide residues, determination in wine and grape juice ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fungicides Bupirimate, Fenarimol, and Vinclozolin were sprayed on Vines. The fruits were harvested 8 and 21 days after the final application and processed to juice and wine. The fungicide residues were determined by filtration of the samples throug XAD-2 after pH adjustment, elution with methylene chloride, and glass capillary gas chromatography with SE-30 as stationary phase. Residue values of the three compounds were reported before and after fermentation. The precision of the analytical method was established by spiking portuguese white wine and spanish grape juice with the three fungicides and Triadimefon. The recoveries were in the range 80%-100%, except for Vinclozolin.
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    Journal of High Resolution Chromatography 4 (1981), S. 183-183 
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    Keywords: Gas chromatography ; Capillary, glass ; End-sealing technique for static coating ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 197-200 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 215-217 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary columns ; Direct method for flavor evaluation ; Aromatic herbs analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple, quick method is described for GC head space evaluation of herbs and drugs. The proposed procedure consists of milling a weighed sample of a certain herb in a glass device like a Braun MXK coffee grinder, modified in such a way that a special gas-tight valve allows the direct sampling of the vapors. Glass capillary columns are used to analyze the head space volatiles. Some preliminary applications of the method are given.
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    Journal of High Resolution Chromatography 4 (1981), S. 232-232 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Static coating ; Sealing method ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 237-239 
    ISSN: 0935-6304
    Keywords: HPLC fluorescence detection ; Pre-column derivatization ; Glibenclamide ; Serum drug levels ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 253-254 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 42-42 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 81-83 
    ISSN: 0935-6304
    Keywords: HPLC bonded phases ; Derivatisation of aminopropyl silica ; Resolution of enantiomers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 308-308 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 38-39 
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    Keywords: Gas chromatography ; Fused silica capillary column ; Activity ; Hydroxylated surfaces ; Dehydroxylated surfaces ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 83-85 
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    Keywords: HPLC ; Nanoliter volume detector ; 1.5 × 10-5 AU noise (0.1 μl 0.1% benzene in methanol) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 95-96 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 132-134 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Ion-pair reversed-phase HPLC ; Chlorhexidine in pharmaceutical preparations ; Quantitation within 0.66-3.41% relative standard deviation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 142-142 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 247-248 
    ISSN: 0935-6304
    Keywords: Gas Chromatography ; No simple relationship found between polarity of polysiloxane phases and N-TFA amino acid butyl esters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work, we have investigated the influence of the polarities and structures of 13 polysiloxanes on the retention of some N-TFA N-butyl esters of amino acids. Gehrke [1] was the first to examine the possible relationship between polarity and retention data of amino acid derivatives for 9 stationary liquid phases. He concluded that the molecular structure of the stationary liquid phase is an important factor determining retention.
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    Journal of High Resolution Chromatography 4 (1981), S. 287-291 
    ISSN: 0935-6304
    Keywords: Thin layer chromatography, TLC ; Ion exchange resin plates/tert-butyl alcohol, H2O, Na2HPO4, Nacl; ethanol, H2O, Na-acetate, NaCl ; Sulfonamides and other chemotherapeutic substances ; Qualitative analysis ; Effect of pH variation on Rf values ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A thin-layer chromatographic method is described for sulfonamides and some other chemotherapeutic compounds. Ion-exchange resin precoated plates (Fixion 50 × 8 Na+, Chinoin, Budapest or Polygram Ionex-25 SA-Na, Macherey-Nagel and Co.,Düren, FRG) are employed with Na2HPO4 or Na-acetate (adjusted to different pH values) containing NaCl and tert-butyl alcohol or ethanol as developing solvent system. For qualitative and/or semiquantitave determinations the chromatograms can be stained: (A) with o-tolidine, after chlorination; (B) with p-dimethylaminobenzaldehyde; (C) with p-dimethylaminocinnamaldehyde.
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    Journal of High Resolution Chromatography 4 (1981), S. 346-347 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; WCOT-glass capillary ; Organophosphorus insecticides ; Pesticides ; Metabolites ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article considers the separation of 23 organophosphorus insecticides to which two metabolites have been added. The high resolution of the column permits detection of the Z and E isomers of three of these insecticides.
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    Journal of High Resolution Chromatography 4 (1981), S. 361-362 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 366-384 
    ISSN: 0935-6304
    Keywords: GC/MS ; Capillary columns, fused silica ; Priority pollutants ; Quantitation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Operational characteristics have been determined for fused silica capillary column (FSCC) GC/MS as applied to “extractable” priority polutants. Chromatographic data show excellent relative retention time (RRT) intralaboratory precision and interlaboratory accuracy when multiple internal standards are empolyed. Potential chromatographic problems, such as column overload and “double peaking”, are addressed. Response factor relative standard deviations (RSD) at 50 ng for most of the extractable priority pollutants over the long term indicated precise determination (i.e. RSD generally ≤ 10%). Linearity was demonstrated over two orders of magnitude for FSCC GC/MS analysis of compounds with relatively low and high RF (response factor) values. Potential quantitative problems, such as saturation, are discussed. For certain aromatic priority pollutants interlaboratory RF agreement was observed. This was noted as perhaps the most important property of FSCC GC/MS analysis when the multiple internal standard approach is utilized. Determinations of extractable priority pollutants are directly compared for paced column GC/MS and FSCC GC/MS analysis of separate and composited extracts. For six extracts analyzed in triplicate, the latter configuration was shown to produce more consistent results. In view of the superior analysis logistics of composite extract FSCC GC/MS analysis, this approach was established as the preferred method for the analysis of priority pollutants classified as extractable.
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    Journal of High Resolution Chromatography 4 (1981), S. 393-397 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, fused silica ; Simultaneous detection ; Splitting capillary effluent ; Detection limit of 1 ppm Archlor 1254 ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A state-of-the-art gas chromatographic system for automatic simultaneous detection of halogenated and normal hydrocarbons has been developed, which consists of a standard Hewlett-Packard 5880 with a fused silica capillary column, whose effluent is split between the standard flame ionization detector and a Tracor Hall electroconductivity detector. The system provedes excellent capillary chromatography results and high sensitivity for halogenated compounds (a detection limit of 1 ppm Archlor 1254 in fuel oil). Reliability has been provides in the daily analysis of complex environmental samples.Emergency response cleanup and the containment of hazardous chemical spills and chemical dump sites forces one to deal with samples that are very complex. The contain large numbers of naturally occurring organic compounds and varying types of organic pollutants. Capillary chromatographic techniques of gas chromatographic and gas chromatographic/mass spectrometric analyses are necessary to achieve the resolution required for the analysis of these samples.
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  • 65
    ISSN: 0935-6304
    Keywords: Thin layer chromatography ; Use of molten solids as mobile phase advantageous ; Migration at higher temperature (80-180°C) studied ; Correction of front position for unsaturated flow possible ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper considers some aspects of a new TLC technique using a molten mobile phase which is solid under ambient conditions. The flow of high-boiling mobile phase at elevated temperature in thin-layer chromatography has been investigated and it is shown that the equation Zf2 = kt is not applicable to migration of the high boiling mobile phase front. The flow stability of the high-boiling mobile phase is noted. It is suggested on the basis of studies of concentration profiles of the solidified mobile phases by scanning photometers that the shape of the mobile phase concentration profile be taken into account in calculation of Rf Values.
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    Journal of High Resolution Chromatography 4 (1981) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 500-507 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Weak anion exchanger ; Octadecyl bonded packing ; Urine analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The analysis of ultraviolet-absorbing constituents in urine was undertaken by anion-exchange and reversed-phase liquid chromatography. A newly developed anion exchanger (TSK-IEX540 DEAE) was used for ion-exchange mode liquid chromatography and its high polarity and physical strength greatly reduced the analysis time. Up to 80 peaks were resolved within 30 min. Hydrophobicity values were used to predict the retention times of acids in reversed-phase mode liquid chromatography.
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    Journal of High Resolution Chromatography 4 (1981), S. 523-524 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Split injection ; Injection time influence ; PAH ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 533-534 
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    Keywords: Gas chromatography ; Capillary, glass ; End-sealing method for static coating ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 532-533 
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    Keywords: Micro high performance liquid chromatography, MHPLC ; Fourier transform infrared spectrometry, FT- IR ; Combination of MHPLC and FT-IR ; KBr buffer memory technique ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 546-546 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 72
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    Journal of High Resolution Chromatography 4 (1981), S. 557-560 
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    Keywords: Thin layer chromatography, TLC, HPTLC ; Reversed phase, chemically bonded ; Phenols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 580-581 
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    Keywords: Gas chromatography ; Coal gasification tar ; Boiling point distribution ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 584-585 
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    Keywords: Liquid chromatography, HPLC ; Reverse-phase mode ; TBAOAc/NH4OAc ion-pairing reagent circumvents problems ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of High Resolution Chromatography 4 (1981), S. 591-594 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 77
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    Journal of High Resolution Chromatography 4 (1981), S. 647-648 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Direct injection of silicone fluids method of choice for determining trace organic contaminants ; ≥ 1 ppm toluene determined ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 78
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    Journal of High Resolution Chromatography 4 (1981), S. 653-654 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Diastereoisomer separation of organic sulfites ; Bis(2-aryl-3-oxotetrahydro-2H-1,2-oxazin-5-yl) sulfite ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 79
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    Journal of High Resolution Chromatography 4 (1981), S. 659-660 
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    Keywords: Thin layer chromatography, TLC ; Quantitation by TLC scanner ; Detection mode, reflection ; Measuring mode, absorbance ; RSD 3% for carbofuran and 1% for quinalphos ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 80
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    Journal of High Resolution Chromatography 4 (1981), S. 3-5 
    ISSN: 0935-6304
    Keywords: Molecular weight distribution ; Polyglycol GC stationary phases ; Carbowax ; Ucon ; Pluronic ; Emulphor ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The width of the molecular weight distribution (MWD) of polymer stationary phases influences their polarity and other gas chromatographic characteristics. The MWD of the most frequently used polyglycol-type stationary phases such as Carbowax, Ucon, Emulphor and Pluronic has been determined and compared. The MWD determined by gel chromatography allows for the characterization of the actual batch of a stationary phase, provides a check on its consistency and helps to screen out the apparently less promising phases.
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    Journal of High Resolution Chromatography 4 (1981), S. 24-26 
    ISSN: 0935-6304
    Keywords: HPTLC ; HPLC ; GC/MS ; Methyl hydroxybenzoate (MHB) ; Propyl hydroxybenzoate (PHB) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Different chromatographic methods for determination of methyl hydroxybenzoate and propyl hydroxybenzoate in pharmaceutical formulations are compared. Procedures for HPTLC, HPLC and GC/MS are given.
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    Journal of High Resolution Chromatography 4 (1981), S. 37-38 
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    Keywords: HPLC ; Cardenolides in Convallaria majalis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cardenolides of Convallaria majalis were separated by reverse-phase HPLC on Partisil PXS 10/25 ODS columns using 25% acetonitrile as mobile phase. Periplorhamnoside, convallatoxin and either convallatoxol or convalloside were resolved from glycoside mixtures. Convallatoxin and periplorhamnoside were identified in plant extracts, convalloside and convallatoxol were not resolved from non-cardenolide material present in leaf extracts.
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    Journal of High Resolution Chromatography 4 (1981), S. 79-80 
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    Keywords: Gas chromatography ; Glass capillary columns ; Barium carbonate ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 84
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    Journal of High Resolution Chromatography 4 (1981), S. 86-89 
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    Keywords: Gas chromatography ; Packed columns ; Multidimensional switching, MDSS ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A multidimensional switching system with two packed columns has been used for the analysis of volatiles. Use of a high-boiling solvent and the backflush mode permitted total resolution of the mixture discussed in a short analysis time.
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    Journal of High Resolution Chromatography 4 (1981) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 102-108 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Series-coupled columns with different stationary phases ; Independent temperature control of columns ; Constant mass flow rate ; Retention time expressions ; Theory ; Selectivity control ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The technique of controlling chromatographic selectivity by the adjustment of column temperatures in systems of series-coupled columns is investigated by means of a general model incorporating the effects of temperature and mobile phase compressibility. In a previous article the performance of series-coupled columns was investigated under conditions of constant overall pressure drop. The present paper, on the other hand, considers systems in which a constant mass flow rate is maintained at all temperatures. The expressions derived for the effective partition coefficient and the retention time are compared with those of the previous paper. The numerical results for two-column systems exhibit the same major trends as those for constant pressure drop. It is shown that the effective partition coefficient is slightly dependent on the mass flow rate.
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    Journal of High Resolution Chromatography 4 (1981), S. 127-129 
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    Keywords: Gas liquid chromatography ; Open tubular capillary columns ; Adsorption and resolution ; Hydrocarbons ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 130-131 
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    Keywords: Liquid chromatography/mass spectrometry ; Atrazine ; Quantification ; Triazine herbicides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 143-145 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 147-148 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 164-168 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Simultaneous detection with effluent splitter ; Element-specific detection ; Petroleum residues ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two glass capillary gas chromatographic systems were equipped with inert effluent splitters which allowed simultaneous data acquisition using nonspecific and element-specific detectors. Simultaneous detection was achieved using the nonspecific flame ionization detector (FID) and the Hall® electrolytic conductivity detector (HECD) operated in either the sulfur-or the nitrogen-specific mode. Typical application of the simultaneous detection system as applied to analysis of petroleum residues is briefly described. The Hall electrolytic conductivity detector can be made element specific for halogen-, sulfur-, or nitrogen-containing compounds. Simultaneous detection enhances the information yield from a single sample injection and proves to be a powerful complementary technique when used with computerized gas chromatography/mass spectrometry.
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    Journal of High Resolution Chromatography 4 (1981), S. 186-187 
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    Keywords: Gas chromatography ; Capillary, glass ; Effluent splitter, preparation of ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 191-192 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 4 (1981), S. 218-223 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Column preparation ; “Split” vs. “on-column” injection ; Amino acid analysis, quantitative 10 ng level ; Average relative standard deviation 1% ; Fish muscle protein analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A carefully Standardized technique is described for the preparation of glass capillary columns which can be used successfully for routine quantitative amino acid analysis. Comparison is made between two different modes of sample injection. Preliminary quantitative results from “split” injection and “on-column” injection techniques are evaluated statistically and it is concluded that the “on-column” system is a prerequisite for quantitative amino acid analysis by glass capillary gas chromatography. An analysis of fish muscle protein hydrolyzate illustrates an application of this technique and results are compared with those from a packed column analysis.
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    Journal of High Resolution Chromatography 4 (1981), S. 224-227 
    ISSN: 0935-6304
    Keywords: Thin-layer adsorption chromatography ; Optimum separation ; Binary mobile phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The measure of the distribution of a mixture of substances in TLC with a binary mobile phase is expressed as ΔRM1,2i,j which represents the difference between the RM values of substances i and j on use of the binary solvent 1 + 2 as the mobile phase. The possibility of determining its maximum value at an optimum composition of the binary mobile phase is demonstrated in this paper. This value can calculated from experimental and theoretical functions RM1,2 = f(Φ1) of substance i and j. More simply, ΔRM1,2i,j can be calculated theoretically from easily measurable adsorption parameters of excess adsorption isotherms and from chromatographic parameters obtained for pure solvents. The ΔRM1,2i,j value calculated theoretically can be utilized in a pilot technique for determination of the optimum composition of the mobile phase in gradient liquid chromatography.
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    Journal of High Resolution Chromatography 4 (1981), S. 437-443 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Gas chromatographic profiles ; n-Butylboronates ; Alkyl-oximes ; Primary prostaglandins ; 6-Keto prostaglandin F1α ; Thromboxane B2 ; Isomers of prostaglandin F1α ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work describes the use of glass capillary columns (GCC) in the rapid concurrent analysis of primary prostaglandins (PGs) (e. g. PGE2, PGE2, PGF2α) and other functionally significant metabolites of arachidonic acid (AA) such as TXB2 and 6-keto PGF1α. The use of a new multistep mixed derivatization approach that generates the methyl esters of n-butylboronate, pentafluorobenzyloxime, trimethylsilyl ether derivatives of these compounds remarkably simplifies the GC profiling of the three main pathways of AA metabolism (PGs, thromboxane, and prostacyclin). Furthermore, isomeric species giving very similar or identical mass spectral patterns can be easily identified by their relative retention times on high efficiency capillary columns.
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    Journal of High Resolution Chromatography 4 (1981), S. 276-279 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Linear elution strength mobile phase technique ; Calculation of eluent compostion ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of gradient elution in RP-HPLC is increasing. Aqueous buffers, such as phosphate at pH 1.7, with acetonitrile as the organic modifier are particularly advantageous as eluents with linear elution strength (LES). In the isocratic mode, under the experimental conditions used, fairly good linearity exists between logk' and xB (xBº is the volume ratio of the organic modifier, i.e. acetonitrile) with a correlation coefficient of 0.9995. The relationship between isocratic and gradient elution parameters, such as xB, xBº (starting composition in gradient elution), m (slope of the linear gradient), is transparent and the parameters of interest can be predicted fairly accurately using simple equations. The proposed system could be used in elaboration of a general retention index system for organic molecules in RP-HPLC.
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    Journal of High Resolution Chromatography 4 (1981), S. 482-482 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 4 (1981), S. 495-499 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary column, fused silica ; Mass spectrometry ; Interface, direct coupling ; On-column injection ; Aflatoxin B1 ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel fused silica capillary GC/MS direct coupling is described which ensures quantitative transfer of sample from the point of injection to the ion source of a mass spectrometer without contacting any surfaces other than the column wall. This device permits GC analysis of highly labile substances. Aflatoxin B1, previously considered unassayable by GC, can now be determined by GC/MS.
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    Journal of High Resolution Chromatography 4 (1981), S. 309-314 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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