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  • Polymer and Materials Science  (956)
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  • 1970-1974  (956)
  • 1950-1954
  • 1972  (956)
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  • 1970-1974  (956)
  • 1950-1954
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 6 (1972), S. 179-250 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 1-14 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The radiation-induced graft copolymerization of styrene and various kraft softwood lignins was studied. Expression of the results as the usual “per cent graft” was impossible, because grafting caused the lignin to become extractable in solvents for the styrene homopolymer. However, evaluation of the effects of various solvents on the degree of reaction was made through an indirect, and possibly more characteristic, measure. Grafting was least pronounced under conditions of low lignin accessibility (e.g., when less than 10% methanol was present), but increased with the addition of better lignin solvents or with higher methanol concentrations. The precipitating nature of the latter conditions was also found to contribute to an accelerated rate of grafting. Surprisingly, the graft copolymer was found to degrade at higher doses. Proof of grafting is offered in a fractionation scheme. Measurement of the molecular weight of the polystyrene separated from the lignin backbone allows the estimation of approximately one polystyrene graft per lignin molecule in benzene-extractable copolymers. Two glass transition temperatures could be detected in several fractionated copolymers.
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  • 4
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 61-68 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Color stability in irradiated PVC may be achieved by (1) structural modification to block dehydrochlorination, (2) addition of radiation protectors, or (3) addition of radical scavengers. This study explores the latter approaches. Twenty-six compounds representing a variety of structural types were screened for their effectiveness as measured by subsequent color development. Fifteen of the compounds imparted partial or complete postirradiation stability. Possible stabilizer mechanisms are discussed.
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  • 5
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 83-97 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The ultraviolet degradation of poly(vinyl chloride) films was studied in a photoreactor which supplied energy near 3000 Å. It was noted that the rate of degradation and color development was increased when the level of residual solvent in the cast films was increased. Two solvents were employed in the study: tetrahydrofuran and dichloroethane. The amount of residual solvent was correlated with the height of a characteristic peak at 2800 Å for tetrahydrofuran and 1900 Å for dichloroethane. Films which had very small traces of solvent showed excellent resistance to ultraviolet degradation, even in the absence of ultraviolet stabilizers. The analysis of solubility data showed that chain scission was controlling in the early stages of exposure, while crosslinking was controlling at later stages. As a result, it was not possible to apply Charlesby's treatment of radiation-induced degradation. Comparison with the results obtained by other workers for degradation at 2537 Å showed that degradation at this wavelength was much faster than degradation at 3000 Å. Furthermore, degradation at 2537 Å appeared to be controlled by crosslinking at all stages of exposure.
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  • 6
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 139-155 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In this paper we define a new structural parameter of polymers, and show how this may be employed. This parameter, for which only the structure and the density are needed, is the relative number of network bonds per unit volume; it is written Ner (basis 1 cm3), and it is used in conjunction with the average connectivity or connection number CN of the network atoms, where the word connection also refers only to network bonds. The relationship of these two numbers makes it possible to present a unified picture of all polymers, organic and inorganic, including such highly condensed networks as diamond. By plotting Ner against CN, the region in which inorganic and organic polymers occur can be seen. This is called the polymer zone, and it is evident that carbon polymers occupy only a small part of it. From this graph, an arbitrary measure of bond packing efficiency can be deduced for carbon polymers. In addition, the process of graphitization and carbonization can be followed graphically within the polymer zone. Ner is also related to certain physical properties such as bulk modulus, hardness, and cubical coefficient of expansion, which depend (among other things) on the tightness of bond arrangement. The resultant correlations can be used to predict the value of Ner required to achieve given values of these properties for the more rigid structures.
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  • 7
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 191-202 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Poly(ethylene terephthalate) has been irradiated with UV light of different wavelengths and in various atmospheres. The extent of degradation was monitored by measuring the tensile strength, molecular weight, carboxylic acid endgroups, and fluorescence emission of the polymer. The importance of wavelengths 〈315 nm in causing deterioration was demonstrated to be mainly due to strong surface absorption which results in surface crazing and ultimate fracture under stress. Irradiation in nitrogen and under vacuum were found to give similar results, but with oxygen present in the system several significant differences were observed. In nonoxidative irradiations, crosslinking and discoloration of the polymer occurred. Under oxidative conditions, chain scissions and fluorescent material build-up resulted, whereas no crosslinking and only slight discoloration was observed. The possibility of a photo-oxidation reaction has thus been suggested, involving hydroperoxide formation, to explain the discrepancy in results obtained for the two types of environments.
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  • 8
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 345-352 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The preparation of 3,3′-dichloro-5,5′-diaminobenzidine and its polymeric reaction products with pyromellitic dianhydride and 3,4,3′,4′-benzophenonetetracarboxylic dianhydride are described. The soluble amine-acid-amide form of the polymer is stable at higher concentrations than the corresponding polymers from 3,3′-diaminobenzidine or 3,3′,4,4′-tetraaminodiphenyl ether. Infrared spectra indicate that polybenzimidazopyrrolone structure is formed after cure. The preparation and properties of films and glass-reinforced laminates prepared from the polymers are described.
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  • 9
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 395-406 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A variance range analysis of the x-ray line profiles for seven cottons (native, ureatreated, and mercerized) has been carried out to get two estimates of the crystallite size from (1) the slope and (2) the variance intercept. Assuming the crystallite length of cellulose to be the same in ramie and native cottons under ideal conditions of growth, the relative fluctuation of the repeat length along the b-axis has been calculated for all the samples. This degree of paracrystalline lattice distortions is negatively correlated with the fiber bundle strength at zero gauge and appears to be the same as the imperfections referred to in the weak link theories of fiber strength. While the orientation parameters are also well correlated with strength, the degree of crystallinity does not seem to have any influence. Wilson's rigorous mathematical treatment of the number-average particle size, in relation to the two estimates from the variance slope and intercept as well as the particle size distribution, has been successfully applied for the first time to cotton fibers leading to a clearer understanding of crystallite size-strength relationship.
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  • 10
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 449-460 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A copolymer (MW = 1800) of styrene (St) and maleic anhydride (MAn) was esterified with an excess amount of an alcohol mixture, and then the relation between the esterification rates of the individual alcohols and the contents of the esters in the esterific copolymer was examined. At first, the rate constant of an individual esterification was obtained for four different alcohols (n-butanol, i-amylalcohol, and benzylalcohol) in a noncatalyst system. Then, the mixed esterification of n-butanol and i-amylalcohol was carried out; from the analysis of the ester contents, the following equation was obtained: $$ {{\left[ {{\rm P}_{\rm 1} } \right]} \mathord{\left/ {\vphantom {{\left[ {{\rm P}_{\rm 1} } \right]} {\left[ {{\rm P}_{\rm 2} } \right]}}} \right. \kern-\nulldelimiterspace} {\left[ {{\rm P}_{\rm 2} } \right]}} = {{k_1 \left[ {{\rm B}_{\rm 1} } \right]_0 } \mathord{\left/ {\vphantom {{k_1 \left[ {{\rm B}_{\rm 1} } \right]_0 } {k_2 \left[ {{\rm B}_{\rm 2} } \right]_0 .}}} \right. \kern-\nulldelimiterspace} {k_2 \left[ {{\rm B}_{\rm 2} } \right]_0 .}} $$ From this result, it was concluded that, in esterification with alcohols involving n species, the content of the individual ester can be expressed by the following equation: $$ {{\left[ {{\rm P}_j } \right]} \mathord{\left/ {\vphantom {{\left[ {{\rm P}_j } \right]} {\sum\limits_{i = 1}^n {\left[ {{\rm P}_i } \right]} }}} \right. \kern-\nulldelimiterspace} {\sum\limits_{i = 1}^n {\left[ {{\rm P}_i } \right]} }} = {{k_j \left[ {{\rm B}_j } \right]_0 } \mathord{\left/ {\vphantom {{k_j \left[ {{\rm B}_j } \right]_0 } {\sum\limits_{i = 1}^n {k_i \left[ {{\rm B}_i } \right]_0 } }}} \right. \kern-\nulldelimiterspace} {\sum\limits_{i = 1}^n {k_i \left[ {{\rm B}_i } \right]_0 } }} $$ where [P] = concentration of esters in the copolymer, [B]0 = initial concentration of alcohols, and k = rate constant of esterification (i,j = 1,2…,n).
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  • 11
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 539-543 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 12
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 865-870 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The difference between the hydraulic permeability K under a pressure gradient and the diffusive permeability P under a concentration gradient can be explained by the incipient viscous flow at high degree of swelling. This flow is opposed by the friction resistance of the macromolecules of the highly swollen membrane. It comes to an end at a critical swelling Hc when the number of permeant molecules is not more sufficient for a complete solvation of the macromolecules of the membrane. Below this swelling, K equals PV1/RT, where V1 is the molar volume of the permeant, and above it the difference K - PV1/RT is proportional to H/(1 - H) - Hc/(1 - Hc). The proportionality factor depends on the friction coefficient of the macromolecular segments and on the average lateral chain clustering. The data on poly(glycerol methacrylate) suggest that on the average the aggregates contain two chains.
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  • 13
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 917-920 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A two-component reactive system consisting of a poly(chromium(III) bisphosphinate) and dioctylphosphinic acid reacts to form a poly(chromium(III) trisphosphinate). Extensive thermomechanical hysteresis is displayed throughout the temperature range -180°C to 〉300°C by specimens containing filaments of glass. Thermal pretreatment to about 400°C (the limit of thermal stability) eliminated these instabilities. These results correlate with the reported brittle and tough character of films of the poly(chromium (III) bisphosphinate) and poly(chromium (III) trisphosphinate), respectively. Regardless of thermal history (between 200°C and 400°C), the polymer system displayed three major transition regions: the glass transition centered at about 0°C, another centered at about 230°C, and a third at about -200°C.
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  • 14
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 945-954 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Sorption kinetics and equilibria for CO2 in polycarbonate were studied over a range of temperatures from 35° to 65°C and pressures from 3 to 22 atm. The dual mode sorption model of Vieth et al. was used to test the data, and a comparison was made with previous work on glassy polystyrene. Further evidence of the validity of generality of the model in providing a consistent picture of small-molecule diffusion in glassy polymers was thereby provided. The technical feasibility of membrane separation of H2 from a H2/CO2 mixture by selective permeation through polycarbonate was examined at 50°C.
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  • 15
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    Journal of Applied Polymer Science 16 (1972), S. 987-1008 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Statistical analysis of inherent viscosities (LVN), shear modulus (G*), and melting temperature (Tm) interval data for isotactic polypropylene-linear polyethylene (HDPE) blends was performed in order to verify their microheterogeneity. High shear measurements in viscometric (Poiseuille's) flow were carried out on four replicated compositions of the blends. Least-squares treatment of the results yielded power law parameters for the blends differing in composition. The significance of differences between the blends of various HDPE content was tested using the multiple-range (Duncan's) test, and tentative conclusions are drawn on the composition dependence of the melt flow viscosities of the blends.
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  • 16
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The radiation-induced graft copolymerization of styrene to cellulose has been studied in vacuo at 30°C and at dose rates from (0.37 to 8.73) × 10-2 W/kg. Dioxan was used as solvent for monomer and polystyrene homopolymer, and water (2% total volume) was incorporated as swelling agent for cellulose. The concentration of styrene in the bulk medium was varied from 0.432 to 3.46 moles/l., and the rates of both grafting and homopolymerization were shown to be proportional to [monomer] · [intensity]1/2. The value of 3.3 × 10-4 l. mole-1 sec-1 derived for kp2/kt in homopolymerization is similar to that for normal free-radical polymerization of styrene. However, reduced termination during grafting yielded a much higher value (58 l. moles-1 sec-1). Degradation of cellulose in the absence of monomer was followed viscometrically, and values of 13.5 and 24.6 were derived for G (scission) in vacuo and in air, respectively.
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  • 17
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The separation of various liquid mixtures including systems of chloroform-hydrocarbons or ethyl ether, water-alcohols and water-nucleophilic organic solvents have been investigated by the pervaporation technique. Membranes were obtained by grafting Lewis base onto poly(tetrafluoroethylene) (PTFE) films. The PTFE backbone has been chosen for its mechanical and chemical resistance. N-Vinylpyrrolidone and 4-vinylpyridine were selected because of their great affinity for the electrophilic compounds. In all cases, the compound which has the greatest affinity for the membrane pervaporates selectively through modified PTFE films. Selectivity and rates were studied. It is concluded that because selectivity is very important, total separation of different mixtures is possible at a good yield, with a faster rate when the temperature is increased or the thickness of the membrane is decreased.
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  • 18
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    Journal of Applied Polymer Science 16 (1972), S. 1109-1123 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polybutadiene rubbers of well-defined and varying molecular weight were prepared by anionic polymerization and used in the preparation of mass-polymerized polystyrene blends. The particle size of the dispersed rubber phase was varied by (1) controlling the relative viscosity, at phase inversion, of the two liquid phases composed of polystyrene and polybutadiene in styrene monomer; (2) by varying the intensity of mixing, and (3) by adding preformed polystyrene to the prepolymer, prior to phase inversion. The mechanical and dynamic properties of the resulting blends are found to be determined mainly by the particle size of the dispersed rubber phase, independently from the method used to obtain such size. The weight fraction of rubber phase, rather than the weight fraction of rubber charged, is found to correlate with the blend modulus and may also affect its level of toughness. Low molecular weight rubbers are found capable of efficient blend reinforcement, if the excessively small rubber particle size obtained by conventional processes is enlarged by incorporation of preformed polystyrene prior to phase inversion.
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  • 19
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    Journal of Applied Polymer Science 16 (1972), S. 1155-1166 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper describes the results of simultaneous dynamic measurements in tension and torsion made on propellant samples. The complex dynamic moduli E′, E″, G′, and G″ at low frequencies were determined within a temperature range from room temperature to -90°C. Time temperature shift factors and reduced master curves for both tension and shear properties are discussed. The effect of dewetting on the dynamic properties in tension and shear was also investigated. A preliminary attempt is made to compute the degree of dewetting in a propellant by applying Beer-Lambert's law.
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  • 20
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    Journal of Applied Polymer Science 16 (1972), S. 1191-1212 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A change in the degree of vulcanization in a carbon black-filled rubber is shown not to affect the change of in-phase shear modulus with strain amplitude, provided the amount of filler is kept constant. Similar results are found with the change of out-of-phase modulus and phase angle with strain amplitude. A similar value of change of in-phase shear modulus with strain amplitude (G′0 - G′∞) is found for a vulcanized and unvulcanized tire tread rubber; this behavior is attributed for the breakdown of the secondary three-dimensional carbon black aggregated network. Detailed consideration is given to other factors such as hydrodynamic, shape factor, and relaxation effects which contribute to the difference between the shear modulus of the gum rubber and the filled rubber when all the carbon black structure has been broken down. The consequence of the breakdown of the secondary aggregated structure of carbon black are considered in terms of factors affecting heat build-up in tires.
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  • 21
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    Journal of Applied Polymer Science 16 (1972), S. 1281-1293 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A semiempirical model for estimation of viscosities of concentrated polymer solutions1 can be applied to mixtures of polymers in a common solvent. The data required for estimation of mixture viscosity are: solvent viscosity, polymer molecular weight, density, concentration, and intrinsic viscosity in the particular solvent. Calculated and experimental viscosities agree to within a few per cent for the relatively nonpolar systems for which comparative data are available. The model does not appear to be adequate for mixtures in which there are extensive hydrogen-bonding interactions.Results of the new model are equivalent to those of an empirical equation2 reported to be effective for fairly concentrated binary polymer mixtures.Specific interactions between polymeric solutes can be conveniently assessed by comparing measured mixture viscosity to that calculated from the model presented. It is not clear, however, that such assessments have any fundamental significance, since the interactions which are calculated depend on the assumptions inherent in the estimation of the “ideal” mixture viscosity. The same reservations apply to other models which have been proposed for this purpose.
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  • 22
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    Journal of Applied Polymer Science 16 (1972), S. 1911-1924 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Equipment and techniques are described which have been developed for determining the drawing behavior of fibers from novel polymers which are available only in very small quantities. Emphasis is placed upon information obtained from the stress-strain diagrams of the fibers during drawing. A parameter, the reinforcement factor, is described which reflects the degree of orientation induced by drawing short lengths of fiber in a discontinuous manner. This parameter exhibits maxima at various combinations of temperature and draw rate, and the relationship between the corresponding temperatures and draw rates is shown to be logarithmic. The parameter is used to predict temperatures and draw rates which will give fibers having a high degree of orientation and good tensile properties when drawn continuously. The application of these techniques to give acceptable fibers from poly(m-phenylene adamantane-1,3-dicarboxamide) is described. This material is of interest as one possessing a high degree of thermal stability, and the best fibers produced to date have a tenacity of 4.0 g per denier, an initial modulus of 60 g per denier, and a break extension of 16.0%.
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  • 23
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    Journal of Applied Polymer Science 16 (1972), S. 1925-1935 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Styrene-grafted nylon 6 fibers which had been prepared by the UV irradiation method were investigated by dynamic viscoelasticity and dilatometry. It was found that nylon 6 is relaxed and polystyrene is simultaneously plasticized by nylon 6 during grafting. These phenomena are interpreted as follows. The grafting process causes nylon 6 to have a lower glass transition temperature and increases grafting frequency of polystyrene to nylon 6 by increasing the chemical junctions between the two components, so that they necessarily become more compatible.
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  • 24
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    Journal of Applied Polymer Science 16 (1972), S. 1947-1952 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The grafting of isoprene as well as a comonomer mixture of isoprene and acrylonitrile onto a backbone of high molecular weight poly(propylene oxide) with tertiary-butyl peroctoate gave a gumstock which is sulfur curable to a product having interesting elastomeric properties.
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  • 25
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    Journal of Applied Polymer Science 16 (1972), S. 1937-1946 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Starch xanthates with degrees of substitution (D.S.) ranging from 0.08 to 0.58 were reacted with high or low molecular weight polyethylenimine (PEI, two of six times the stoichiometric amount) to form starch poly(ethylenimino thiourethanes). Aqueous thiourethane solutions were mixed with commercial styrene-butadiene and acrylonitrile-butadiene latices, and the solids were coprecipitated by adding 1M ZnSO4 and 1N H2SO. The master batches (filtered, dried at 70°C), having 15 to 50 parts of starch (equivalent) per 100 parts of rubber (phr), were masticated and compounded in a sulfur-accelerator recipe and press cured to yield vulcanizates of improved physical characteristics compared to control vulcanizates. About 0.22 D.S. produced best results. With this D.S. xanthate and a 3.5 ratio of 100,000 MW PEI, a 25 phr starch loading gave maximum tensile strength (2720 psi) in a styrene-butadiene vulcanizate. Hardness generally increased with increasing D.S. and starch contents. The thiourethane decreased compression set and increased abrasion resistance. The former was lowest and the latter highest at ca. 0.20 D.S. and 25 phr starch. Both set and abrasion were lowest with thiourethane prepared from xanthate made in a “Roto-feed” process rather than a “Ko-Kneader” operation. Rebound was not appreciably changed, and increase of volume swelling in water was small upon thiourethane incorporation.
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    Journal of Applied Polymer Science 16 (1972), S. 1953-1958 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of epoxy resins based on the diglycidyl ethers of bisphenol A have been characterized by nuclear magnetic resonance and gel permeation chromatography. The ratio of molecular volume of a lightly branched molecule to that of a linear molecule of the same weight was found to vary as the square root of the ratio of the average maximal dimensions of the chain. At high degrees of chain branching, the ratio of the latter was to the power of three halves.
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    Journal of Applied Polymer Science 16 (1972), S. 1959-1965 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics of primary crystallization from the melt of nylon 6-piperazine adipate and nylon 6-piperazine terephthalate copolyamides were measured dilatometrically. It was found that the crystallization rate of the samples under investigation decreases with increase in the percentage comonomer content and rigidity of molecules over the entire temperature range investigated. The Avrami exponent n varied with temperature, values being from 2 to 4.
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    Journal of Applied Polymer Science 16 (1972), S. 2091-2104 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermomechanical spectra of two series of amorphous polyolefins represented by $\rlap{--} [{\rm CH}_2 )_m {\rm - C}\left( {{\rm CH}_3 } \right)_2 \rlap{--} ]_n$ and $\rlap{--} [\left( {{\rm CH}_2 } \right)_m \bond {\rm C}\left( {{\rm CH}_3 } \right)\left( {{\rm C}_2 {\rm H}_5 } \right)\rlap{--} ]_n$, where m = 1, 2, and 3, are presented from -180°C to above the glass transition temperatures. The polymers were obtained by cationic polymerization of α-olefins. The mechanical spectra show a maximum in glass transition temperature and secondary transition temperature for the second member of each series. This maximum is interpreted in terms of a proposed geometrical intermolecular interlocking which is considered to be at a maximum for the second member of the series and serves to restrict the submolecular motions associated with the transitions. The proposal is discussed in terms of its consequences upon free volume, density, cohesive energy density, and chain flexibility.
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    Journal of Applied Polymer Science 16 (1972), S. 2131-2139 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The proton spin-lattice relaxation and dielectric relaxation were studied in some polymers at the solid-polymer interface was constructed from several filled polymers. A useful model of surface layer which can be considered as consisting of a great number of small solid particles covered with a polymer layer. The following systems were studied: polystyrene, poly(methyl methacrylate), their copolymers and cellulose acetate in the presence of different content of fine particles of aerosil and Teflon. It was established that the decrease of surface layer thickness shifts the minimum of spin-lattice relaxation time T1 of high temperature process to higher temperature and minimum T1 of low temperature process to lower temperature. The same was found for dielectric losses reflecting the motion of side groups and of segments. From temperature dependence of T1 and tan δ for both relaxation processes the apparent energies of activation were calculated. On the base of dielectric relaxation data the circular diagram of complex dielectric constant was constructed and by the Cole-Cole method the dispersion parameter α for polymers at the interface was calculated. These data also show the broadening of relaxation spectra in surface layers. The results are discussed in terms of the restriction of possible conformation of chains at the interface and their interaction with surface. It was established that character of molecular motion changes at the interface is dependent on the mode of molecular motion.
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    Journal of Applied Polymer Science 16 (1972), S. 2153-2155 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 16 (1972), S. 2175-2184 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Capillary flow data were obtained for a 27.5% solution of cellulose acetate in acetone. The solution temperature was 50°C, and the range of apparent shear rates investigated was 1.7 × 105 to 1.7 × 106 sec-1. Capillaries having tapered entrance angles of 37.88° to 120.63° were used. A power-law model was adequate to describe the shear stress at the wall (τw) and the corrected shear rate \documentclass{article}\pagestyle{empty}\begin{document}$(\dot \gamma )$\end{document} relationship. Entrance angle affected the entrance pressure drop corrected for kinetic energy, (ΔP0,c); ΔP0,c increased as the angle widened. Treating the entrance flow as an elongational flow situation facilitated superposition of the Delta;P0,c data on a single curve. Estimated elongational viscosities decreased with increasing applied stress.
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    Journal of Applied Polymer Science 16 (1972), S. 2159-2173 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Differential thermal analysis, or DTA, is a technique for determining the properties of materials from the thermodynamic and kinetic points of view. Dielectric measurement is also a powerful tool for probing the structure of materials, but from another direction. Dielectric analysis is a measure of the dipole response within dielectric materials to an applied electric field. This response is controlled by the spatial arrangement and viscoelastic properties of dielectric materials. Dielectric thermal analysis is being increasingly used in research and process control, offering the advantages of being nonobtrusive and easily instrumented and having a broad theoretical basis which can be correlated with results from other methods such as dynamic mechanical relaxation measurements, NMR, neutron relaxation, birefringence, and, of course, DTA. Because of the nonobtrusive nature of dielectric measurement, it can be run concurrently with other analytical techniques without disturbing their results. When dielectric analysis is run concurrently with other methods of analysis such as DTA, we often receive fresh insights and cross-checking on such behavior as polymeric crosslinking, molecular weight increase, and Tg - viscoelastic behavior in general. The results and conclusions drawn for such investigations are described.
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    Journal of Applied Polymer Science 16 (1972), S. 2207-2213 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Contact angles are reported for the systems ethanol-water, n-propanol-water, and benzene-cyclohexane measured at atmospheric pressure and 25.0°C, in equilibrium with their vapors, on poly(tetrafluoroethylene) surfaces of known roughness. Comparison of the data with those reported by other workers has shown that the discordancy in values can be attributed solely to the various preparation techniques producing surfaces of differing roughnesses.
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    Journal of Applied Polymer Science 16 (1972), S. 2239-2247 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The compatibility of the mixtures poly(vinyl chloride) - ethylene vinyl acetate copolymer and poly(vinyl chloride) - chlorinated ethylene vinyl acetate copolymer was studied by the method of dynamic mechanical testing. The character of G′ and G″ was confronted with the Takayanagi model. In all cases a limited compatibility of the components was observed.
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    Journal of Applied Polymer Science 16 (1972), S. 2249-2255 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The applicability of the formula f(t) = n(t)RT(α - α-2) suggested by Tobolsky as the basis of chemorheology has been discussed. In this expression, f(t) is the stress after t hours, n(t) is the crosslinking density (mole/cc) after t hours, R is the gas constant, T is the absolute temperature, and α is the extension ratio. We have discussed the applicability of this formula, in another words, whether the degraded stress f(t) calculated from this formula would be consistent with the initial stress ft(0) of other polymer if the degraded crosslinking density values n(t) are equal to those of nt(0), the initial density values n(0) of other polymer. Natural rubber vulcanizates and SBR vulcanizates were used as samples in these experiments. Assuming n(t) = σ(t) n(0), α(t′) = 1, the applicability of the above formula was recognized from our experimental results.
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    Journal of Applied Polymer Science 16 (1972), S. 2257-2268 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effects of the combination of solvent and nonsolvent on the column fractionation of polypropylene were investigated. Decalin, kerosene, and α-chloronaphthalene were employed as the solvents, whereas ethyl and butyl carbitol were employed as the nonsolvents. It was found that the molecular weight distribution of the fractions was not very significantly affected by the combination of solvent and nonsolvent. By applying Caplan's theory, namely, that M̄-1/2 is a linear function of the weight fraction of solvent contained in the eluent (where M is the average molecular weight of a fraction), we concluded that to conduct a good fractionation both the solvent and the nonsolvent should be poorer solvents for the polymer.
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    Journal of Applied Polymer Science 16 (1972), S. 2291-2315 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An apparatus was constructed which would allow vinyl-type monomers (and others) to polymerize at ambient temperatures in the presence of an inductively coupled RF field. The details of the construction of the system are reported along with preliminary results obtained from nine monomers: styrene, methylvinyldichlorosilane, vinyl acetate, acrylonitrile, vinyl fluoride, 1,1-difluoroethylene, vinyl chloride, ethylene, and 1,3-butadiene.
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    Journal of Applied Polymer Science 16 (1972), S. 2317-2341 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study has been made on the plasma polymerization of styrene monomer in a cold, low-power, inductively coupled RF plasma. Styrene monomer yielded an insoluble, crosslinked film which was slightly colored. A kinetic study is reported for styrene. The effects of power level, bleed rate of monomer, pressure, and reactor geometry on the rate of polymer formation are reported. A mechanism is postulated for plasma polymerization. It was found that the initiation step was the rate controlling step and that the reaction followed a cationic polymerization scheme. Both crosslinking and discoloration of the polymers occur at the time of polymerization and are not a result of exposure of the reacted polymer to the plasma. The polymerization was shown to take place in the bulk phase as well as on the reaction wall surfaces.
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    Journal of Applied Polymer Science 16 (1972), S. 2269-2290 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The phenomenon of plasticizer acceptance by poly(vinyl chloride) (PVC) in hotprocess dry blending is examined via scanning electron microscopy, mercury intrusion porosimetry, and torque rheometer measurements. The effects of granule porosity, resin molecular weight, and synthesis recipe in PVC manufacture by the suspension process are related to the rate of plasticizer acceptance. For a PVC resin to dry blend, i.e., to become a free-flowing powder when mixed with plasticizer under hot-processing conditions, the resin granules must be porous. Porosity arises from interstices between primary PVC particles. At a given granule porosity, an increase in primary particle agglomeration adversely affects dry blend performance. At constant molecular weight and for resins manufactured by a given recipe, dry-blend performance is quantitatively described by granule porosity. With an increase in resin molecular weight, a greater granule porosity is required to maintain an equivalent dry-blend time (DBT). Accordingly, for most suspending agent recipes, DBT is dependent directly upon granule porosity and inversely upon molecular weight. However, if the suspending agent used in resin manufacture is an excessively rapid film former, dry-blend performance with molecular weight variation is dependent upon the suspending agent's concentration, not upon granule porosity, which must be adequate, nor upon the resin's molecular weight. An interfacial film-forming suspending agent enhances fusion of primary PVC particles at the suspension granule - water interface, increasing the granule's “pericellular membrane” thickness. This membrane, a PVC skin, does not significantly influence dry-blend performance with low- or intermediate-viscosity plasticizers. The particle skin does impede dry-blend rates with high-viscosity, poorly solvating plasticizers, but this effect can be negated in part by increasing the diameter of pore openings in the topographical skin. Dry blending occurs below the glass transition temperature (Tg) of PVC with low-viscosity plasticizers and above the Tg with high-viscosity, poorly solvating modifiers. The influence of resin and plasticizer variables indicates the dry-blend phenomenon to be a diffusion-controlled process. The rate of dry blending is dependent upon two mechanisms: (1) the rate of pore penetration - which exposes the plasticizer to a much greater surface area than if it remained exterior, encapsulating the granule - and (2) the rate of plasticizer diffusion into the PVC matrix.
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    Journal of Applied Polymer Science 16 (1972), S. 2353-2359 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A high-density polyethylene prepared at low pressures is characterized with respect to density, microscopic examination, mechanical properties, and diffusion. The data for the slowly cooled, nonisothermally crystallized polymer clearly indicate that the method of preparation grossly affects the final properties of the polymer.
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    Journal of Applied Polymer Science 16 (1972), S. 3003-3016 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Osmotic pressure experiments were conducted with PVC samples of different molecular weights dissolved in THF, using both a block osmometer and a Hewlett-Packard automatic osmometer equipped alternately with Schleicher and Schuell 07 and 08 membranes to optimize the procedure for accurate osmotic pressure measurements. It was found that, provided a flow of solvent could be maintained through the membrane and into the solution, an osmotic pressure of good accuracy was obtained even though the membrane was nominally much too coarse for the polymer analyzed.
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    Journal of Applied Polymer Science 16 (1972), S. 3035-3038 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 16 (1972), S. 3039-3040 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 16 (1972), S. 3041-3046 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Journal of Applied Polymer Science 16 (1972), S. 3017-3034 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Earlier work revealed that the internal plasticization of polyacrylonitrile by the higher n-alkyl acrylates or N-n-alkylacrylamides yielded only brittle copolymers. This difficulty was circumvented in the present work by starting with copolymers of acrylonitrile and ethyl acrylate, over the range of compositions, and further modifying these by incrementally displacing the ethyl acrylate in each recipe by n-octadecyl acrylate through terpolymerization. In this way, the stepwise small reduction in Tg for the base ethyl acrylate-acrylonitrile copolymers was greatly increased for each of the terpolymers. Compositions were obtained ranging from glassy, brittle terpolymers, with glass transitions above room temperature, to soft plasticized polymers having sufficient polar networks retained from the nitrile to confer useful properties. The decline in the glass temperature was shown to be dependent on the free volume conferred by the side-chain methylene groups of each acrylate ester. In contrast, the decline in tensile and flexural strengths and moduli for the terpolymers having glass transitions above room temperature was produced entirely by the presence of the methylene groups of the 18-carbon ester. The glass transition region corresponded to room temperature when the acrylonitrile content of the base copolymer had been reduced to 50 mole-%. Terpolymers of this nitrile content and lower had the low moduli and large elongations of plasticized compositions. An equation was developed which correlated empirically the glass transitions and the mechanical properties with the weight fraction of the acrylate esters for the glassy terpolymers.
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    Journal of Applied Polymer Science 16 (1972), S. 3047-3062 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The problem of drag reduction in a helically coiled tube is examined experimentally. The general problems involved in the correlation of drag reduction data are analyzed critically, and some important recommendations are made based on the findings of this work. A phenomenological approach is suggested for correlating the drag reduction data. An examination of the straight-tube data from the literature and the coiledtube data obtained in this work shows that for a variety of aqueous polymer solutions the data could be uniquely correlated by the following equation: \documentclass{article}\pagestyle{empty}\begin{document}$ \beta = 0.2 + \frac{{0.8}}{{1 + \left( {{\rm De'}} \right)^{0.8} }} $\end{document} where β = reduced friction factor and De′ = modified Deborah number.
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    Journal of Applied Polymer Science 16 (1972), S. 3063-3071 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The ultraviolet absorption spectra of Cadoxen solutions of hydrocellulose and hydrocellulose phenylosazones are described. With solutions of hydrocellulose no simple relationship between D.P. and absorbance was found. Solutions of hydrocellulose phenylosazone in Cadoxen show well-defined maxima at 277 nm and 390 nm and do not change over 1 hr when oxygen is excluded. The absorbance of the phenylosazone at 390 nm may be used to determine the D.P. of the hydrocellulose samples.
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    Journal of Applied Polymer Science 16 (1972), S. 3073-3094 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermomechanical spectra of two new carborane-siloxane polymers containing five-boron carborane cages in the backbones are reported and discussed. The polymers are the homopolymer, HO—[Si(CH3)2—CB5H5C—Si(CH3)2—O—]nH, and the random copolymer with 20 mole-% of the ten-boron meta-carborane analogue, —[Si(CH3)2—CB10H10C—Si(CH3)2—O—]. The mechanical spectra (∼1 cps) were determined from -180° → +625° → -180°C (ΔT/Δl = 3.6°C/min for T 〉 25°C and 2°C/min for T 〈 25°C) using the semimicro thermomechanical technique, torsional braid analysis. In nitrogen, both polymers displayed secondary transitions at -140°C. The glass transition (Tg) for the homopolymer was -60°C and for the copolymer was -52°C. The homopolymer had a melting point of +70°C. The copolymer was amorphous. The high-temperature stability in nitrogen of both polymers appeared to be identical; thermal stiffening commenced at 400°C, continued to 625°C, and resulted in materials that were typical of highly crosslinked resins. In air, the homopolymer began to stiffen catastrophically near 270°C, while the copolymer began to stiffen similarly nearly 50°C higher. The intrinsic elastomeric nature together with the thermomechanical results prompted further study of the copolymer. Thermomechanical cycling studies in nitrogen and air are reported for the copolymer. Some correlating TGA and DTA are also discussed.
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    Journal of Applied Polymer Science 16 (1972), S. 3095-3103 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Nine linear poly(carborane-siloxane) high-temperature elastomers which differ systematically in chemical structure were investigated by torsional braid analysis. The structural variations include two different carborane cage structures in the polymer chain (—CB10H10C— and —CB5H5C—) and the stepwise increase in the number of —Si(CH3)2—O— linkages associated with each cage in the repeat unit. Poly(dimethylsiloxane) was studied as the compositional limit of both series. The dynamic mechanical relaxations (at about 1 cps) of the materials are reported. These include the melting points of the semicrystalline polymers and the glass transitions and secondary transitions of all the polymers. The glass transition temperatures in each series were systematized using the well-known copolymer composition-versus-glass transition temperature relationship 1/Tg = W1/Tg1 + W2/Tg2.
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  • 50
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    Journal of Applied Polymer Science 16 (1972), S. 3113-3121 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The interaction of the acid dye Biebrich Scarlet (C.I. Acid Red 66) with α-, β-, and γ-keratoses obtained from wool fiber by performic acid oxidation was studied. The extrapolated saturation values of dye bound to protein and the association constants for the interactions were obtained. Maximum dye uptake was found for α-keratose, followed by γ- and β-keratoses, in that order. Incorporation of varying amounts of m-cresol in the dye solutions showed no significant effect. There was no indication of an interaction between m-cresol and the keratoses from direct studies.
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    Journal of Applied Polymer Science 16 (1972), S. 3123-3131 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The thermal stabilities of polybutadienyllithium, polyisoprenyllithium, and polystyryllithium solutions have been determined in hydrocarbon solvents. Kinetic analysis indicated that a complex mechanism was involved in the thermolysis of polybutadienyllithium. The thermal stability was observed to increase with increasing lithium concentration, suggesting the presence of competitive reactions in addition to the expected elimination of lithium hydride. The thermal stability of the three systems studied was consistent with their reported degrees of association: dimeric polystyryllithium was less stable than tetrameric polyisoprenyllithium or hexameric polybutadienyllithium.
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    Journal of Applied Polymer Science 16 (1972), S. 3133-3144 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In addition to the expected elimination of lithium hydride, metalation and addition reactions have been observed as competitive, thermolytic reactions of polybutadienyllithium. The importance of these reactions at temperatures frequently utilized for the polymerization of butadiene was illustrated and the effect of these reactions on the macrostructure of polybutadiene determined.
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  • 53
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    Journal of Applied Polymer Science 16 (1972), S. 3207-3221 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The products obtained on degradation of poly(p-N,N-dimethylaminostyrene) in vacuo are described. The effects of molecular weight and pyrolysis temperature are discussed and the behavior compared with polystyrene under similar conditions. Product analysis has revealed significant differences between the products of degradation obtained from the two polymers, and mechanisms involving methyl-group migration have been proposed and discussed to account for the anomalous behavior of poly(p-N,N-dimethyl-aminostyrene). The liquid products of pyrolysis have been separated and identified by gas-liquid chromatography using the Kovats retention index, and quantitative analysis is also described. Analysis of the gaseous fraction by mass spectrometry is described.
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    Journal of Applied Polymer Science 16 (1972), S. 3223-3236 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect of the extent of degradation of poly(p-N,N-dimethylaminostyrene) on the quantity and composition of the residue and the effect of pyrolysis temperature on the fraction volatile at pyrolysis temperature are discussed. The behavior of poly(p-N,N-dimethylaminostyrene) is compared to that of polystyrene. A significant difference has been found for the behavior of the residue from poly(p-N,N-dimethylaminostyrene), which is ascribed to a crosslinking reaction involving the dimethylamino substitutent. Mechanisms to account for the observed products of degradation have been suggested and are discussed.
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    Journal of Applied Polymer Science 16 (1972), S. 3237-3244 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Fibers were spun from six different, wholly aromatic copolyamides of limited order. Tensile properties of the fibers were obtained at standard conditions and, for selected fibers, at elevated temperatures and after heat-aging at 300°C in air. The dry-heat shrinkage determined up to 400°C on selected fibers was relatively low; zero-strength temperatures ranged from 375°C to 495°C. Resistance to numerous chemical reagents was determined for one of the fibers and found to be comparable to that of the fibers from other wholly aromatic polyamides. Resistance to ultraviolet light appeared to be of the same order as that of unstabilized nylon 66.
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    Journal of Applied Polymer Science 16 (1972), S. 3245-3251 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: On the basis of Mooney scorch measurements at 120°C and of continuous measurements of vulcanization in a Vuremo curemeter at 145°C, sulfenamides which function as inhibitors of the sulfur-free thiuram vulcanization have been investigated. It was found that the actual prevulcanization inhibitor is 2-mercaptobenzothiazole. Its formation from sulfenamides is activated by zinc dimethyldithiocarbamate since the vulcanization of rubber by thiuram disulfides in the presence of zinc oxide is always accompanied by the formation of zinc dithiocarbamate. It seems probable that the inhibition effect of 2-mercaptobenzothiazole is attributable to the formation of a complex with zinc dimethyldithiocarbamate which decreases the reaction rate in the initial steps of the sulfur-free thiuram vulcanization and thus causes the scorch delay.
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    Journal of Applied Polymer Science 16 (1972), S. 3265-3274 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermal decomposition and resultant disposal of waste poly(vinyl chloride) (PVC) is facilitated by preliminary exposure to ionizing radiation, such as energetic electrons, in an oxygen atmosphere. The results of isothermal and temperature-programmed thermogravimetry, differential thermal analysis, and effluent gas analysis in nitrogen and in oxygen indicate that the major effect of irradiation is to render PVC increasingly susceptible to oxidation. The presence of oxygen during heating enhances the decomposition. Crystalline order in PVC is destroyed by irradiation.
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    Journal of Applied Polymer Science 16 (1972), S. 3253-3263 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The kinetics of simultaneous thermal and hydrolytic degradation of poly(1,4-cyclohexylenedimethylene terephthalate) (PCHDT) were evaluated by using a 1.5-in.-diam. melt extruder (≈20/1 length/diameter ratio) as a reactor. The effects of extrusion temperature (295°-330°C), residence time (2.6-17.5 min), and moisture content (〈0.001% to 0.2%) of the supply polymer on degradation were determined. The rate of degradation was measured in terms of the rate at which inherent viscosity (I.V.) decreased and the rate at which carboxyl endgroup concentration increased. The contributions of both thermal and hydrolytic degradation to the total degradation of PCHDT could be separated because the hydrolysis was rapid enough that it could be considered as occurring prior to thermal degradation. Thus, the hydrolysis merely adjusted the initial properties of the supply polymer, which was then subjected to thermal degradation. Equations were developed from an analysis of the kinetic data based on a random chain scission mechanism. The activation energies for decrease in I.V. and increase in carboxyl endgroup concentration of PCHDT from thermal degradation were determined as 33.5 and 41 kcal/mole, respectively.
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    Journal of Applied Polymer Science 16 (1972), S. 3353-3360 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Two independently derived distribution function methods validate both the calibration curve and the dispersion correction of the “effective linear calibration” method used in gel permeation chromatography (GPC). Experimental conditions are specified for making the method more useful by permitting linear extrapolation of the calibration line, \documentclass{article}\pagestyle{empty}\begin{document}$ V_R = C_1 + C_2 \log M, $\end{document} and for using a minimum number of standards. The independent methods quantitatively relate known differential of integral distribution functions for standard samples to their respective chromatograms. As such, they are useful calibration methods also, but are limited in scope and range.
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    Journal of Applied Polymer Science 16 (1972), S. 3381-3385 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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    Die Makromolekulare Chemie 158 (1972), S. 27-37 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zur Untersuchung der Kinetik der radikalischen Polymerisation des Acrylamids bei Monomerkonzentrationen unter 0,1 m wurde ein spezielles Dilatometer konstruiert. Die Initiierung der Polymerisation erfolgte durch 4.4′-Azo-bis-4-cyanovaleriansäure in wäßriger Lösung bei 25°C.Aus den m't einem Testversuch der Anfangskonzentrationen [M] = 0,093 m und [I] = 2,09·10-3 m bestimmten Ausdehnungs- und Viskositätsdaten konnte ein fkd-Wert von 2,81·10-8 sec-1 berechnet werden. Ein Vergleich mit extrapolierten Literaturangaben für kd bei 25°C ergab einen Wirkungsgrad f von 0,65 Die fkd- und f-Werte in dieser Untersuchung sind vergleichbar mit anderen veröffentlichten Angaben.Die gefundene Polymerisationsgeschwindigkeit von der Ordnung 3/2 in bezug auf die Konzentration [M] zeigt, daß die Ordnung für Monomerkonzentrationen unter 0,1 m größere Werte als 1 annimmt. Die Ergebnisse können im Rahmen der Käfig-Effekt-Theorie erklärt werden.
    Notes: A dilatometer was constructed to study the free radical polymerization kinetics of acrylamide below 0.1 M monomer. The polymerization was initiated by 4.4′-azo-bis-4-cyano-pentanoic acid in aqueous solution at 25°C.The fkd value, calculated from dilatometric and viscometric data for a test with initial concentration [M] = 0.093 M and [I] = 2.09·10-3 M, was 2.81·10-8 sec-1. Comparison with an extrapolated literature value for kd at 25°C indicated an efficiency value, f, equal to 0.65. Both fkd and f were comparable in magnitude to results of other cited investigations.The results of a 3/2 order dependency of polymerization rate on [M] substantiated the apparent tendency of acrylamide concentration exponents to increase above 1.0 below 0.1 M monomer. A cage effect theory was offered as an explanation for this phenomenon.
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    Die Makromolekulare Chemie 162 (1972), S. 219-233 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Gegenstand dieser Arbeit war die Untersuchung der Änderung der Feinstruktur von isotaktischem Polypropylen während der isothermen Kristallisation und die Feststellung, ob die Theorie der durch die Kristallisation induzierten Molekularfraktionierung oder die der durch die Translationsdiffusion der Polymerkette im Kristallzustand hervorgerufenen Lamellenverdichtung (Translationsdiffusionstheorie) bei dem Kristallisationsprozeß die entscheidende Rolle spielt. Mit fortschreitender Kristallisation entstehen unabhängig vom Molekulargewicht und der Molekulargewichtsverteilung bei niedriger Temperatur schmelzende Kristalle. Bei Polymeren mit hohem Molekulargewicht wird das Maximum der Wärmekapazität zu höheren Temperaturen hin verschoben; die hoch schmelzenden Komponenten entstehen im wesentlichen über den Translationsdiffusionsmechanismus. Sofern der Unterschied der Molekulargewichte zweier Komponenten einer Polymermischung nicht zu groß ist, findet man im DSC-Thermogramm einer solchen auskristallisierten Mischung ein Maximum, das in erster Näherung in der Mitte zwischen den Maximum der unter den gleichen Bedingungen wie die Mischung auskristallisierten getrennten Komponenten liegt. Sofern sich die Molekulargewichte der beiden Komponenten wesentlich unterscheiden, zeigt das DSC-Thermogramm der Mischung, daß beide Komponenten die Tendenz getrennt zu kristallisieren aufweisen. Die von KAWAI, HOSOI und KAMIDE für lineares Polyäthylen auf experimentellem Wege erhaltenen Hinweise gegen die Fraktionierungstheorie werden am Beispiel des isotaktischen Polypropylens im Detail untersucht.
    Notes: The objects of this study were to examine the change of the fine structure in isotactic polypropylene during isothermal crystallization and to determine whether the theory of molecular weight fractionation induced by crystallization or the lamellae thickening, due to longitudinal translation or sliding diffusion of polymer chains in a crystal state (sliding diffusion theory) is important in the crystallization process. As crystallization proceeds, low melting crystals are produced, irrespective of molecular weight and molecular weight distribution. For high molecular weight polymers, the peak of the thermogram shifts to higher temperatures, and the high melting components are produced mainly by the sliding diffusion mechanism. If the difference between the molecular weights of both components in a polymer blend is not too great, a peak is found in the DSC thermogram of such a crystallized blend which occurs roughly midway between those of each separately component crystallized under the same conditions as the blend. If the molecular weights of the two components differ greatly the DSC thermograms of the blend show that each component tends to crystallize separately. The experimental evidences, obtained by KAWAI, HOSOI, and KAMIDE in the case of linear polyethylene, against the fractionation theory are examined in detail for isotactic polypropylene.
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    Die Makromolekulare Chemie 162 (1972), S. 269-274 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: By means of light scattering measurements the second osmotic virial coefficient A2 is determined for two series of cellulose trinitrate with somewhat different nitrogen content (CTN 13.9 and CTN 12.9) as a function of temperature. The individual contributions A2,H and A2,S obtained therefrom show considerable negative values for the excess entropy in some cases. Enthalpy and excess entropy of dilution are found to be closely correlated.
    Notes: An zwei Reihen von Cellulosetrinitraten mit etwas verschiedenem Stickstoffgehalt (CTN 13,9 und CTN 12,9) wird der zweite osmotische Virialkoeffizient A2 in Abhängigkeit von der Temperatur durch Streulichtmessungen bestimmt und daraus die Anteile A2,H und A2,S berechnet. Es treten z. T. erhebliche negative Werte der Exzeßentropie auf. Zwischen der Exzeßentropie der Verdünnung und der Verdünnungsenthalpie besteht eine deutliche Korrelation.
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    Notes: No Abstract
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    Die Makromolekulare Chemie 158 (1972), S. 223-239 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Thiocarboxylic acid trimethylsilyl esters (I and II) are obtained by the conversion of carboxylic acid chlorids or anhydrids with hexamethyl disilthian. The trimethylsilylesters I and II react with various electrophilic reagents like acid chlorides or alkyl bromides under elimination of halogen silane yielding always the S-acyl or S-alkyl derivatives of the thiocarboxylic acids. By the reaction of α.ω-dithiodicarboxylic acid trimethylsilyl esters (II) with their corresponding dicarboxylic acid chlorides hitherto unknown polyacylsulfides are formed. Similarly the following polyamides are obtained by the reaction of thea II and piperazine biscarbamoylchloride.
    Notes: Durch Umsetzung von Carbonsäurechloriden oder -anhydriden mit Hexamethyldisilthian lassen sich Thiocarbonsäure-trimethylsilylester (I und II) herstellen. Die Silylester I und II reagieren mit verschiedenen elektrophilen Reagenzien, z B. mit Säurechloriden und Alkylbromiden unter Eliminierung von Halogensilan, wobei stets Thiocarbonsäure-S-acyl-oder -S-alkylderivate entstehen. Aus α.ω-Dithiocarbonsäure-trimethylsilylestern (II) und den zugehörigen Dicarbonsäurechloriden wurden bisher noch nicht beschriebene Polyacylsulfide gewonnen; bei der Umsetzung mit Piperazin-bis-carbonylchlorid entstehen Polyamide (s. Summary).
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    Die Makromolekulare Chemie 158 (1972), S. 313-316 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
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    Die Makromolekulare Chemie 159 (1972), S. 1-5 
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    Die Makromolekulare Chemie 159 (1972), S. 18-28 
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    Die Makromolekulare Chemie 159 (1972), S. 66-79 
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    Die Makromolekulare Chemie 159 (1972), S. 79-81 
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    Die Makromolekulare Chemie 159 (1972), S. 102-107 
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    Die Makromolekulare Chemie 159 (1972), S. 82-102 
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    Die Makromolekulare Chemie 159 (1972), S. 107-125 
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    Die Makromolekulare Chemie 159 (1972), S. 133-141 
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    Die Makromolekulare Chemie 159 (1972), S. 141-150 
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    Die Makromolekulare Chemie 159 (1972), S. 125-132 
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    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Wird ein aus Monomereinheiten A bestehendes Homopolymeres durch eine polymeranaloge Reaktion in ein Copolymeres der Monomereinheiten A und B umgewandelt, so kann die reversible Reaktion A ⇄ B in ihrer Kinetik von den beiden benachbarten Monomereinheiten abhängen. Es wird gezeigt, daß in den Copolymeren eine regellose Verteilung der Blöcke entlang der Kette vorliegt in dem Sinne, daß die Wahrscheinlichkeit eines Blockes bestimmter Länge nicht von der Länge benachbarter Blöcke abhängt. Im Gegensatz zur regellosen Verteilung der Blöcke in der Kette entspricht die Häufigkeitsverteilung der Blocklänge einer nicht-MARKOFFschen Statistik der Monomereinheiten. Ein exaktes Schema für die Anwendung von bedingten Wahrscheinlichkeiten zur Berechnung der Wahrscheinlichkeiten von Sequenzen wird angegeben. Eine Methode zur Ableitung der Geschwindigkeitsgleichungen für polymeranaloge Reaktionen und deren Anwendung zum Beweis der regellosen Statistik der Blöcke wird beschrieben. Durch Monte-Carlo-Simulation erhaltene Modellcopolymere bestätigen die regellose Statistik der Blöcke und die nicht-MARKOFFsche Statistik der Monomereinheiten.
    Notes: When converting a homopolymer, consisting of monomer units A, by a polymer analogous reaction into a copolymer, composed of monomer units A and B, the reversible reaction A ⇄ B may be kinetically influenced by the two flanking monomer units. The distribution of the blocks along the chain of the copolymer is shown to be random in the sense that the probability of a block of given length does not depend on the length of adjacent blocks. As opposed to the random distribution of the blocks in the chain, the frequency distribution of the block lengths conforms to block probabilities determined by a non-MARKOVian statistics of monomer units. The exact way to use conditional probabilities for calculating the probabilities of sequences is presented. A method for deriving rate equations of polymer analogous reactions and their use for proving the random distribution of the blocks is described. Model copolymers obtained by Monte Carlo simulation of polymer analogous reactions confirm the random statistics of blocks and the non-MARKOVian statistics of monomer units.
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  • 78
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    Die Makromolekulare Chemie 160 (1972), S. 183-194 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die ungestörten Dimensionen von Blockcopolymeren aus Polystyrol und Polyisopren in verdünnten Lösungen wurden aus unter Theta-Bedingungen durchgeführten Messungen und unter Anwendung der FLORY-FOX-Theorie über Viskositätsdaten bestimmt. In Lösungen, bei denen die Theta-Temperaturen eine direkte Bestimmung ausschließen, wurde die STOCKMAYER-FIXMAN-Methode angewandt. Die Ergebnisse zeigen, daß die unter Theta-Bedingungen ermittelten ungestörten Dimensionen sich - unabhängig davon, ob die Bestimmung direkt oder durch Extrapolation erfolgte - linear mit der Zusammensetzung ändern. Demzufolge kann das charakteristische Verhältnis des Blockcopolymeren aus den für die Homopolymeren gegebenen Werten gemäß der Gleichung \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm c}_\infty ^{{\rm Block}} {\rm } = {\rm xc}_\infty ^{{\rm PS}} {\rm } + {\rm (1 - x)c}_\infty ^{{\rm PI}} $\end{document} bestimmt werden. Hierin ist x der Molenbruch; die hochgestellten Indices PS und PI beziehen sich auf Polystyrol bzw. auf Polyisopren. Der sterische Faktor σ = r02rof2 gehorcht einer entsprechenden Beziehung. Nahwechselwirkungsparameter wurden durch Anwen-dung von Gleichungen, die die zweiten osmotischen Virialkoeffizienten mit dem ausge-schlossenen Volumen verkniipfen und die sich bei der Auwendung auf Homopolymere als sinnvoll erwiesen haben, ermittelt. Die uber Viskositatsmessungen einerseits und uber osmometrische Methoden andererseits erhaltenen Daten werden miteinander verglichen und diskutiert.
    Notes: The unperturbed dimensions of block copolymers of polystyrene and polyisoprene in dilute solution have been determined from measurements made under theta conditions, by application of the FLORY-FOX theory to viscosity data. In solvents, where theta temperatures preclude direct evaluation, the STOCKMAYER-FIXMAN method has been applied. The results show that unperturbed dimension determined under theta conditions, whether measured directly or by appropriate extrapolation procedures, vary linearly with composition. Thus the characteristic ratio for the block copolymer may be calculated from homopolymer data according to the relation \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm c}_\infty ^{{\rm Block}} {\rm } = {\rm xc}_\infty ^{{\rm PS}} {\rm } + {\rm (1 - x)c}_\infty ^{{\rm PI}} $\end{document} where x is the mole fraction and superscripts PS and PI refer to polystyrene and polyisoprene respectively. The steric factor σ = r02rof2 obeys a similar relation.Short range interaction parameters have also been determined by application of equations relating osmotic second virial coefficients with the excluded volume and which have been shown to be reasonably successful when applied to homopolymers. Data from viscosity and osmometry methods are compared and discussed.
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  • 79
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    Die Makromolekulare Chemie 160 (1972), S. 213-225 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die elektrophile Desaktivierungsreaktion eines „lebenden“ monocarbanionischen Polystyrols mit Tris(allyloxy)1.3.5-triazin führt zur Bildung sternförmiger Polymerer, in welchen drei Polystyrolketten mit den drei C-Atomen des Triazinrings verbunden sind. Die molekularen Eigenschaften dieser Polymeren werden durch osmometrische, viscosimetrische und Lichtstreuungs-Messungen sowie durch Gel-Chromatographie charakterisiert. Daraus geht eindeutig hervor, daß bei dieser Reaktion wohldefinierte Modell-Polymere mit sehr enger Molekulargewichtsverteilung erhalten werden. Die hydrodynamischen Eigenschaften dieser Stern-Polymeren werden mit den theoretischen Voraussagen verglichen.
    Notes: La réaction de désactivation électrophile d'un polystyrène «vivant» monocarbanionique sur le tris(allyloxy)1.3.5-triazine, conduit à la formation de molécules en étoile à trois branches dans lesquelles les branches sont liées aux trois atomes de carbone d'un hétérocycle triazine. La détermination des caractéristiques moléculaires de ces polymères par osmométrie, diffusion de la lumière, viscosimétrie et par chromatographie sur gel (GPC), montre que des molécules-modèle de structure bien définie et de très faible polydispersité ont été obtenues. Les propriétés hydrodynamiques de ces polystyrènes en étoile sont étudiées et comparées aux prévisions théoriques.
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  • 80
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    Die Makromolekulare Chemie 160 (1972), S. 251-258 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Grenzflächenpolykondensation von Silanen mit Hydrazinen wurden Polymere der Struktur I hergestellt. Dabei kam ein modifiziertes wasserfreies Lösungsmittelsystem aus Acetonitril und Kohlenwasserstoffen zur Anwendung.Die Produkte haben nur niedrige Molekulargewichte. Eine Zuordnung der IR-Banden wird gegeben.
    Notes: Polymers of the form below were prepared by the interfacial method via the condensation of silanes with hydrazines employing a modified nonaqueous system using acetonitrile and liquid hydrocarbons. IR frequency band assignments are given. The products are oligomeric.
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  • 81
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    Die Makromolekulare Chemie 160 (1972), S. 321-338 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurde die Kinetik der Reaktion des Bis(4-isocyanatophenyl)methans (MDI) und des 1-Methyl-2.4-diisocyanatobenzols (2.4-TDI) mit Poly(oxyäthylen) (POE, M̄n = 2750) sowie mit Poly(oxyäthylenoxyadipoyl) (PAE, M̄n = 2350) in Toluol oder Dioxan bei konstantem Verhältnis [NCO]/[OH] = 2 untersucht. Bei Wahl bestimmter experimenteller Bedingungen können „Präpolymere“ mit Isocyanat-Endgruppen erhalten werden. Die Stabilität dieser Polymeren ist jedoch begrenzt. Eine Nebenreaktion führt zur Erhöhung des Molekulargewichtes und zur Bildung neuer funktioneller Gruppen, als Folge der Bildung intermolekularer Allophanat-Bindungen. Dieser Prozeß verläuft schneller im Falle des POE als im Falle des PAE.Die Polykondensation eines „Präpolymeren“, PAE, ω,ω′-Diisocyanats und eines POE führt zu linearen Block-Copolymeren, in denen die mittlere Zahl der Sequenzen (3 bis 20) sowie die Länge der POE-Sequenzen weitgehend (2750 ≤M̄n ≤ 10600) variieren können. Die Struktur dieser Polymeren ist charakterisiert durch regelmäßiges Alternieren hydrophober PAE- und hydrophiler POE-Blöcke, die durch Urethanverbindungen miteinander verbunden sind. Diese Produkte sind interessante Modelle auf dem Gebiet kristallisierbarer amphipatischer Block-Copolymer und der Polyurethan-Elastomeren.
    Notes: Nous avons étudié la cinétique de la réaction du bis(4-isocyanatophényl)méthane (MDI) et du l-méthyl-2.4-diisocyanatobenzène (2.4-TDI) sur le poly(oxyéthylène) (POE, M̄n = 2750) et le poly(oxyéthylèneoxyadipoyl) (PAE, M̄n = 2350) en solution dans le toluène ou le dioxanne, et pour un rapport constant [NCO]/[OH] = 2. Il est possible d'obtenir, dans des conditions expérimentales bien déterminées, des «prépolymères» porteurs de groupements terminaux isocyanate. Ces «prépolymères» présentent cependant une stabilité limitée dans le temps, qui se manifeste par un accroissement de la masse moléculaire moyenne et de la fonctionnalité, résultant de la formation de liaisons allophanate intermoléculaires. Ce processus est en particulier accéléré dans le cas des POE.La polycondensation en solution homogène entre «prépolymère» PAE ω.ω′-diisocyanate et POE conduit à des copolymères séquencés linéaires, dans lesquels le nombre moyen de séquences (3 à 20) et la longueur de la séquence POE (2750 ≤ M̄n ≤ 10600) peuvent varier dans un assez large domaine. L'architecture de ces macromolécules est caractérisée par l'alternance régulière de séquences hydrophobes PAE et hydrophiles POE reliées entre elles par des charnières uréthane. Ces matériaux constituent des modèles intéressants dans le domaine des copolymères séquencés cristallisables doués de propriétés amphipatiques, et dans celui des élastomères polyuréthane.
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    Die Makromolekulare Chemie 160 (1972), S. 347-348 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Die Makromolekulare Chemie 158 (1972), S. 39-51 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Epitaxie von Poly-α-benzyl-L-glutamat (PBLG) auf der (001)-Spaltfläche von Alkalihalogenideinkristallen führt zum Aufwachsen von Block- und Linienstrukturen, welche für verschiedene Lösungsmittel und Trägermaterialien qualitativ ähnlich sind. Im Anfangsstadium der epitaktischen Kristallisation wurde eine eindeutige Tendenz zur Orientierung der α-Helices von PBLG entlang der 〈110〉-Richtung des Trägers beobachtet. Es wird angenommen, daß die epitaktischen Strukturen aus gestreckten, nicht gefalteten Molekülen (α-Helices) gebildet sind, die normalerweise nebeneinander, im Fall von niedermolekularen Fraktionen aber auch linear assoziiert sind. Epitaxie von PBLG wurde nur in der Nähe des Fällungspunktes beobachtet. Die vom Kristall ausgehenden Anziehungs-und Orientierungskräfte sind ziemlich weitreichend, und es gibt mindestens zwei Arten davon. Man kann den Dekorationseffekt der PBLG-Epitaxie zur Charakterisierung der Trägeroberfläche ausnutzen.
    Notes: Epitaxial crystallization of poly-γ-benzyl-L-glutamate (PBLG) on 001 alkali halide single crystal surfaces results in block and row structures that are qualitatively similar for various solvents and crystals used. There is a definite tendency in the first stages of epitaxial crystallization to align the α-helical molecules along the 〈110〉 substrate direction. We propose that the epitaxial structures are built up of straight, non-folded α-helical molecules associated side-by-side and, in the case of low M̄w fractions, also end-to-end. The epitaxial crystallization of PBLG was observed only in the vicinity of the precipitation point. The orienting and attracting forces coming from the crystal substrate have a long range character and are of at least two kinds. The decoration effect of PBLG epitaxial structures could be used for substrate surface structure characterization.
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  • 84
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    Die Makromolekulare Chemie 158 (1972), S. 53-63 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Konformation von Poly-L-glutaminsäure (PLGA) in Pyridin/Wasser-Gemischen wurde mit Hilfe verschiedener Techniken untersucht (ORD, IR, NMR und Viskosimetrie). Es wurde gefunden, daß bei niedrigen Wassergehalten PLGA Aggregate bildet, deren Stabilität sehr empfindlich von der Temperatur und der Zusammensetzung des Lösungsmittelgemisches abhängt. Bei höherem Wassergehalt des Mediums findet eine Helix-Knäuel-Umwandlung statt.
    Notes: The conformational state of poly-L-glutamic acid (PLGA) in the mixed solvent pyridine/water has been studied by means of different techniques (ORD, IR, PMR, and viscosity). It has been found that at low water contents PLGA forms aggregates the stability of which depends in a sensitive manner on temperature and solvent composition.At higher water content PLGA undergoes a helix-coil transition.
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    Die Makromolekulare Chemie 158 (1972), S. 65-79 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Diffusion von Helium, Sauerstoff, Stickstoff und Kohlendioxid in Polymethylmethacrylat wurde untersucht. Die erhaltenen Daten wurden nach der von PAUL und DIBENEDETTO modifizierten Methode ausgewertet. Verschiedene thermodynamische Parameter wurden berechnet. Der Mechanismus des Diffusionsprozesses wird diskutiert.
    Notes: Diffusion of helium, oxygen, nitrogen, and carbon dioxide in poly(methyl methacrylate) has been studied. The data are analyzed employing the new modified time-lag technique developed by PAUL and DIBENEDETTO. Different thermodynamic parameters have been evaluated and the mechanism of gaseous diffusion has been discussed.
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  • 86
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The light-scattering-function of salty DNA-solutions indicate a wide-range order in the solution. This order is developing gradually in the solution at rest within a time of several hours to several days. Stirring causes distortion of the lattice. By heating near to the melting point it disappears. From the measured extremes in the scattering function, a BRAGG-value of 6000 Å can be calculated, but periodic distances of 2000 Å and 3300 Å respectively are also possible. In the concentration range from 1 · 10-4 to 3 · 10-4 g/ml no clear dependence on the concentration can be detected, so a model of equidistant parallel rods can be excluded. Immediately after filtration through a planar filter having pores of 0.5 μm in diameter, the DNA-molecules appear to be strongly distorted and are rather coillike.
    Notes: Aus der Winkelabhängigkeit der Lichtstreuung von salzhaltigen DNA-Lösungen kann auf das Vorliegen von Fernordnungen in der Lösung geschlossen werden. Diese Ordnung bildet sich in den ruhenden Lösungen im Verlauf mehrerer Stunden bis Tage aus. Sie kann durch Rühren gestört werden und verschwindet in der Nähe der Schmelztemperatur der DNA.Aus den gemessenen Extremwerten der Streufunktion läßt sich formal ein BRAGGscher Wert von 6000 Å errechnen, aber auch Periodizitäten von 2000 Å bzw. 3300 Å sind möglich. Zwischen 1 · 10-4 bis 3 · 10-4 g/ml läßt sich keine eindeutige Abhängigkeit von der Konzentration feststellen, wodurch man hier ein einfaches Parallelstranggitter ausschließen kann. Unmittelbar nach der Filtration durch Flächenfilter der Porenweite 0,5 μm zeigen die DNA-Moleküle stark gestörte, knäuelartige Struktur.
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  • 87
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    Die Makromolekulare Chemie 158 (1972), S. 113-121 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: We tried to utilize the photolysis of azides to prepare polymers. In this aim, several bis-azides were prepared and photolyzed in different solvents while the calculated amount of nitrogen was split off. Most of the dark-coloured photoproducts were insoluble, while some products from the photolysis were partly soluble in dichloroacetic acid. The structure of the soluble photoproducts was elucidated by comparing the absorption spectra of their solutions with those of a model compound.
    Notes: Es wurde versucht, die Photolyse von aromatischen Aziden zur Darstellung von Polymeren auszunutzen. Zu diesem Zweck wurden mehrere Bis-Azide hergestellt und in verschiedenen Lösungsmitteln bestrahlt, wobei die berechnete Menge Stickstoff abgespalten wurde. Die meisten der tiefgefärbten Bestrahlungsprodukte sind unlöslich; bei bestimmten Ausgangsverbindungen konnten in Dichloressigsäure lösliche Anteile erhalten werden. Auf die Struktur der Bestrahlungsprodukte kann durch Vergleich der Spektren dieser Lösungen mit denen einer Modellverbindung geschlossen werden.
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  • 88
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    Die Makromolekulare Chemie 158 (1972), S. 97-112 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Viscosity measurements with solutions of poly(methyl methacrylate) in toluene are evaluated according to the model of the entanglement network solution. For a comparison, for the same system a numerical calculation of the complete BUECHE function is carried out. There is no break in the η0 vs. M function, but rather a transition, whose breadth depends, among others, upon the slip factor s. Comparison of the numerical results with the data leads to a reasonable value for the frictional coefficient of a chain segment. From the data of the measurements, the critical molecular weight Mc is determined, and therefrom the apparent statistical chain element A′m. It agrees satisfactorily with values from other investigations.
    Notes: Viskositätsmessungen an Lösungen von Polymethylmethacrylat in Toluol werden nach dem Modell der Netzwerk-Lösung ausgewertet. Zum Vergleich wird für dasselbe System eine numerische Berechnung der von BUECHE angegebenen Beziehung durchgeführt; es ergibt sich im η0-M-Verlauf kein Knick, sondern ein Übergang, dessen Breite unter anderem von dem Schlüpffaktor s abhängt. Der Vergleich von Rechnung und Meßdaten ergibt einen vernünftigen Wert des Segment-Reibungsfaktors f0. Aus den Meßwerten wird weiter das kritische Molekulargewicht Mc ermittelt und daraus das scheinbare statistische Fadenelement A′m, das mit Werten aus anderen Messungen befriedigend übereinstimmt.
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    Die Makromolekulare Chemie 158 (1972), S. 123-134 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The FRIES rearrangement was investigated with the acetyl derivatives of some phenolic di- and trinuclear compounds. Using nitrobenzene as solvent and AlCl3 as catalyst, all acetyl groups of a molecule can react to form p-hydroxyacetophenone units. Methoxy groups remain unchanged under these conditions. The conversion to o-hydroxyacetophenone compounds, which generally requires higher temperatures, could not be attained until now. All compounds obtained were investigated by means of IR-, UV- and NMR- spectra. They were further characterized by preparing acetyl derivatives and 2.4-dinitrophenylhydrazones.
    Notes: Die FRIES sche Verschiebung wurde an den Acetylderivaten einiger phenolischer Zweiund Dreikernverbindungen untersucht. In Nitrobenzol, mit AlCl3 als Katalysator, ist bei Temperaturen von 40-60°C eine gleichzeitige Umlagerung von mehreren Acylgruppen pro Molekül in die para-Stellung zur phenolischen Hydroxylgruppe ohne Schwierigkeiten möglich. Methoxygruppen bleiben dabei erhalten. Die bei höheren Temperaturen verlaufende Umlagerung in die ortho-Stellung zur phenolischen Hydroxylgruppe gelang jedoch bisher nicht. Die erhaltenen Mehrkernverbindungen mit p-Hydroxyacetophenonbausteinen wurden IR-, UV- und NMR-spektroskopisch untersucht. Sie wurden ferner durch Überführung in die entsprechenden O-Acetylderivate und 2.4-Dinitrophenylhydrazone charakterisiert.
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    Die Makromolekulare Chemie 158 (1972), S. 161-164 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Einige geschützte, in organischen Solventien lösliche 9-Vinyladenine wurden hergestellt. Diese Monomeren sollen für die Synthese von stereoisomeren Poly-(9-vinyladeninen) eingesetzt werden.
    Notes: In order to develope synthetic approaches to poly-(9-vinyladenines) of varying degrees of stereoregularity a series of protected 9-vinyladenine monomers have been synthesized which are soluble in organic solvents.
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    Die Makromolekulare Chemie 158 (1972), S. 165-175 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: An iterative calculation procedure for the determination of the molecular weight distribution function from experimental, by isothermal elution generated data - especially for narrow distributed polymers - is described. Therein the classically gained distribution is used as an approximation. It is again fractionated by calculation taking as base the phase equilibrium. The calculated fractions give some more information for the construction of a better approximation. Some simulation has been done to show the stability of convergency of this procedure. Finally the method is demonstrated and discussed on experimental data of a mixture of two well known narrow distributed polystyrens.
    Notes: Ein iteratives Rechenverfahren zur Bestimmung der Molekulargewichtsverteilungsfunktionen aus experimentellen, mit der isothermen Elution ermittelten Daten - speziell für Polymere kleiner Uneinheitlichkeit - wird beschrieben. Hierbei wird die klassisch gewonnene Verteilung als Näherung betrachtet, rechnerisch auf der Basis des Phasengleichgewichts erneut fraktioniert und aus den ermittelten Fraktionen die Zusatzinformation zur Konstruktion einer besseren Näherung gewonnen. Um die Stabilität der Konvergenz des Verfahrens zu zeigen, wurde eine Simulationsrechnung durchgeführt. Schließlich wird das Verfahren an experimentell gewonnenen Daten eines aus zwei gut bekannten, eng verteilten Polystyrolen erzeugten Gemisches demonstriert und diskutiert.
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: On a étudié la structure et la cristallisation d'un copolymère triséquencé poly-ε-caprolactone/polyoxyéthylène/poly-ε-caprolactone, dont les séquences, toutes capables de cristalliser, ont des longueurs équivalentes.Grǎce à la dilatométrie et à la diffractométrie selon DEBYE-SCHERRER, on a montré que les deux types de séquences cristallisent effectivement et dans un ordre qui dépend de la température de l'expérience. On a défini trois domaines de température: au-dessous de 51°C, c'est le polyoxyéthylène qui cristallise en premier; au-dessus de 52°C, c'est au contraire la polycaprolactone qui cristallise en premier; entre 51 et 52°C enfin les deux séquences semblent cristalliser en měme temps.A l'aide de la diffractométrie aux petits angles de BRAGG, on a montré que la structure du copolymère est lamellaire et correspond à l'empilement périodique et alterné de couches de polyoxyéthylène et de polycaprolactone. On a de plus établi que, dans la zone intermédiaire de températures de cristallisation, le système résulte de la juxtaposition de domaines entiers comportant des lamelles soit du type de celles obtenues au-dessous de 51°C, soit du type de celles obtenues au-dessus de 52°C.En calculant les taux de cristallinité respectifs des deux séquences du copolymère, on a constaté que ceux-ci ne sont élevés, et en tout cas comparables à ceux des homopolymères correspondants, que dans la mesure où les séquences considérées ont cristallisé avant les autres.Dans une tentative de description plus détaillée de la structure, on a calculé les épaisseurs respectives des couches de polyoxyéthylène et de polycaprolactone, et, dans chacune d'elles, des sous-couches de polymère cristallin et amorphe.En étudiant par dilatométrie la fusion du copolymère, on a constaté que les deux types de séquences fondent indépendamment, d'abord les séquences de polyoxyéthylène, puis celles de caprolactone.Dans une dernière partie, on a considéré enfin le phénomène de recuit. Par suite de la fusion précoce du polyoxyéthylène et de la lenteur extrěme de la polycaprolactone à recuire, le copolymère n'évolue guère par chauffage à température élevée.
    Additional Material: 9 Ill.
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  • 93
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    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 162 (1972), S. 199-204 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Struktur der mittels anionischer Polymerisation von Methacrylsäure-p-tolylester in Toluol oder Tetrahydrofuran (THF) mit Butyllithium, Naphthalinnatrium oder Lithiumaluminiumhydrid als Starter erhaltenen Poly(methacrylsäure-p-tolylester) wurde mit Hilfe der IR- und NMR-(100-MHz)-Spektroskopie bestimmt. Die Polymerisationen in Toluol geben Polymere mit überwiegend isotaktischer Struktur, während die in THF erhaltenen Polymeren hauptsächlich syndiotaktisch sind.
    Notes: La structure des poly(méthacrylates de p-tolyl) obtenus par polymérisation anionique du méthacrylate de p-tolyl dans le toluène ou le tétrahydrofuranne (THF) en utilisant le butyllithium, le naphtalène sodium ou l'hydrure de lithium aluminium comme amorceurs, a été déterminée à l'aide de la spectrographie dans l'infra rouge et de la spectrographie de RMN 100 MHz. Les polymérisations dans le toluène donnent des polymères à structure isotactique prédominante, tandis que dans le THF les polymères obtenus sont essentiellement syndiotactiques.
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  • 94
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Following the syntheses of HAYES and HUNTER a cyclic, tetrameric compound (VII) was prepared by ring closure of a linear four nuclear compound (VI), starting from p-cresol and formaldehyde. The structure of VII was investigated by spectroscopic analysis. By means of UV -and IR- spectra, VII can be distinguished from the starting compound VI and a side product, VIII. The H-NMR-spectra of the cyclic condensate and its starting compound VI are totally identical with the supplied structures. Determined at 20 and 60°C, they give information about certaing conformers of the cyclic compound. The molecular weight (480) received by mass spectroscopic measures, is identical with the calculated value (480,6).
    Notes: In Anlehnung an den Syntheseweg von HAYES und HUNTER wurde eine cyclische, tetramere Verbindung (VII) über eine linear 4-Kernverbindung (VI) (aus p-Kresol und Formaldehyd) hergestellt. Ihre Struktur wurde spektroskopisch untersucht. Mittels UV- und IR-Spektren läßt sich VII von der Ausgangsstufe VI und einem Konkurrenzprodukt VIII unterscheiden. Die H-NMR-Spektren der Ringverbindung und ihrer Ausgangsverbindung (VI) stimmen vollständig mit den angegebenen Strukturformeln überein; sie geben, bei 20 und 60°C aufgenommen, Hinweise auf bestimmte Konformere der Ringverbindung. Das massenspektrometrisch bestimmte Molekulargewicht (480) stimmt mit dem berechneten (480,6) überein.
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  • 95
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Bei der Copolymerisation von D- und L-Alanin-N-carboxyanhydrid (NCA) mit einem überschuß des L-Antipoden mit Hilfe von Triäthylaluminium wurde ein Polyalanin mit gleichen Mengen an L- und D-Resten im Anfangsstadium der Polymerisation erhalten.Als lnitiierung der Polymerisation wird die Wasserstoffabspaltung aus der NH-Gruppe des NCA durch das Trialkylaluminium angesehen.Da Sarcosin-NCA (N-Methylglycin-NCA) nicht mit Trialkylaluminium polymerisiert, wird angenommen, daß die Polymerisation über die Form des metallierten NCA erfolgt. Eine stereochemische Untersuchung des Diisobutylaluminium-Derivats von 4-Methyl-oxazolidon (BAO) als Modellsubstanz für das metallierte NCA zeigte, daß BAO vorzugsweise zu einer meso-dimeren Struktur assoziiert. Daraus wird geschlossen, daß auch das metallierte NCA vorzugsweise eine meso-dimere Struktur ausbildet. Damit stimmt überein, daß die NCA-Polymerisation im Anfangsstadium Polyalanin mit praktisch gleichen Mengen an L- und D-Resten bildet.
    Notes: In the copolymerization of D- and L-alanine N-carboxy anhydride (NCA) with an excess of L-antipode by triethylaluminum, a polyalanine containing an equal amount of L- and D-residues was obtained in the early stage of the polymerization.Initiation of the polymerization was the hydrogen abstraction from NH group of the NCA by the trialkylaluminum.Since sarcosine NCA (N-methylglycine NCA) was not polymerized with trialkylaluminum, alanine NCA is considered to be polymerized through the form of the metalated NCA. A stereochemical study on diisobutylaluminum 4-methyloxazolidonate (BAO) as a model compound of the metalated NCA showed that BAO was associated with each other forming preferentially a meso-dimeric structure. From this result, the metalated NCA is also considered to form preferentially a meso-dimeric structure in conformity with the observed fact that the NCA polymerization produced in the early stage the polyalanine consisting of practically the same amount of L- and D-residues.
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  • 96
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    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 158 (1972), S. 215-222 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Grenzflächenkondensation wurden Polyarylate aus dem Säurechlorid des Methyldi-(p-carboxyphenoxymethyl)-phosphinoxides (MCPO) und verschiedenen Diphenolen erhalten. Die höchsten Molekulargewichte wurden mit 0,1 mol · l-1 Dichlorid und 0,05 mol · l-1 Bisphenol erreicht. Synthetisiert wurden außerdem Copolyarylate aus 2.2-Bis-(p-hydroxyphenyl)-propan, Terephthaloyldichlorid und MCPO, und zwar bei verschiedenen Molverhältnissen. Die erhaltenen Homo- und Copolyarylate weisen sehr gute selbstlöschende Eigenschaften und verhältnismäßig hohe thermische Stabilität auf.
    Notes: Polyarylates were prepared from methyl-di(p-carboxyphenoxymethyl)phosphine oxide (MCPO) acid chloride and bis-phenols by the interphase polycondensation method The highest molecular weights were obtained at an MCPO acid chloride concentration of 0.1 mole·l-1 and a concentration of the bisphenol of 0.05 mole · l-1. Copolyarylates were also synthesized from 2.2-bis(p-hydroxyphenyl)propane, MCPO and terephthalic acid chloride employing different mole ratios of monomers. The homo- and copolyarylates obtained possess well expressed self-extinguishing properties and enhanced thermostability.
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  • 97
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    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 158 (1972), S. 241-260 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Einige wichtige statistische Parameter der wahrscheinlichsten und der TUNG schen Verteilung in bezug auf die Polymolekularität wurden verglichen. Darüber hinaus wurde eine Interpretationsmethode der Fraktionierungsangaben gezeigt die relativ einfach und schnell die Entscheidung ermöglicht, ob eine wahrscheinlichste oder eine TUNG sche Verteilung vorliegt.
    Notes: Some important parameters of the most probable and the TUNG distributions with respect to the molecular heterogeneity have been compared. Furthermore an interpretation method of the fractionation data has been given allowing to decide relatively simply and quickly whether the tested distribution is either of the most probable or the TUNG type.
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  • 98
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Mechanismus der Initiierung der anionischen Polymerisation von 2-Vinylpyridin durch Diphenylnatrium wurde untersucht. Er ist auf Grund der großen Reaktivität der Pyridinringe sehr verwickelt. Diese können ein Elektron aufnehmen und Pyridin-Radikalionen bilden, deren Dimerisation zur Bildung von 4.4′-Dipyridyl führt. Jedoch ist die Synthese von linearen Blockcopolymeren aus 2-Vinylpyridin und Propylensulfid mit drei Blöcken möglich.
    Notes: Le mécanisme d'amorçage de la polymérisation anionique de la vinyl-2 pyridine par le biphényle sodium a été étudié. Il est très complexe en raison de la grande réactivité des cycles pyridiniques. Ceux-ci peuvent capter un électron pour donner des ions radicaux (pyridine) dont la dimérisation conduit finalement à la formation d'enchaǐnements 4.4′-bipyridile. Cependant, la synthèse des copolymères linéaires de la vinyl-2 pyridine et du sulfure de propylène comportant trois séquences est possible.
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  • 99
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Initiierung der anionischen Polymerisation von 2-Vinylpyridin durch Diphenylmethylnatrium wurde spektrophotometrisch untersucht. Diphenylmethylnatrium reagiert nicht mit den Pyridinringen; seine Umsetzung ist unvollständig, weil die Wachstumsgeschwindigkeit erheblich größer ist als die Initiierungsgeschwindigkeit. Die Ergebnisse werden durch die Synthese linearer AB-Blockcopolymerer aus 2-Vinylpyridin und Propylensulfid bestätigt.
    Notes: La réaction d'amorçage de la polymérisation anionique de la vinyl-2 pyridine par le diphénylméthyl sodium a été étudiée par spectrophotométrie. Le diphénylméthyl sodium ne réagit pas avec les cycles pyridiniques mais, par contre sa conversion est incomplète, la vitesse de propagation étant bien supérieure à la vitesse d'amorçage. La synthèse de copolymères biséquencés linéaires de la vinyl-2 pyridine et du sulfure de propylène confirme ces résultats.
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  • 100
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    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 159 (1972), S. 150-150 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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