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  • Polymer and Materials Science  (10)
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  • Polymer and Materials Science  (10)
  • Chemistry  (10)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3605-3616 
    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: Cast amorphous one mil films of poly(ethylene terephthalate)were allowed to crystallize isothermally in silicone oil over the temperature range 25-240°C. The crystallization paths were followed by recording the percent of transmission of 4000 A. light through the films as a function of time at specific temperatures. At temperatures between 70 and 90°C. the transmission increased to a value higher than the initial transmission and did not decrease with time. From about 95 to 125°C. the curves showed a similar increase, followed by a decrease to a minimum and then an increase to a new maximum before leveling off. The shapes of these curves were interpreted in terms of the sizes of the growing spherulites. The first detectable signs of crystallization were observed at 96.5°C., as evidenced by density and densitometer measurements. It is shown that the polymer passed through a temperature range beginning at the glass transition point (66°C.) and extending to about 95°C., where molecular and chain rearrangements occurred without crystallization. Half lives and rate constants were found to increase exponentially over the range 96.5-119.5°C. Above approximately 125°C., the crystallization process took place at such a rapid rate that accurate data were impossible to obtain. Activation energies were calculated from the rate constants and from an estimation of induction times from the light transmission-time curves. These values were found to be 37 and 30 kcal./mole, respectively. The density-time data were also fitted to the Avrami relationship. Evaluation of the constants indicated that the initial crystallization growth was lineal.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3617-3624 
    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: Electron micrographs were made from replicas taken from the natural, argon-etched, and fractured surfaces, respectively, of the polymer before and after progressive stages of crystallization. The natural surface protrusions were identified as axialities and became more defined as the crystallization progressed. The argon-etched surfaces of highly crystallized polymer did reveal the crystalline nature of the polymer, but replicas of the slightly crystalline material gave patterns which cannot be quantitatively described at this time. It is thought that heat effects and/or interactions with the argon ions had an effect on the polymer surfaces. Replicas of the fractured amorphous samples revealed a typical conchoidal fracture, whereas those of the fractured surfaces of the highly crystalline samples gave tangible evidence that this polymer crystallized in a characteristic spherulitic manner.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2799-2804 
    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 transmission electron microscopy (TEM) and scanning electron microscopy (SEM) study of plasma-formed polyethylene and polystyrene is reported. A two-phase structure of spheres embedded in a polymer binder is evident, supporting the predictions of earlier low-angle x-ray scattering data taken of these two plasma-deposited polymers.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2793-2798 
    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 low-angle x-ray scattering technique has been applied to determine the submicrostructure of plasma-formed polyethylene and polystyrene. The plasma-formed polymers appear to closely approximate a “filler - binder” structure where polymer spheres constitute the filler material and a lower-density polymer, the binder. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) micrographs confirm the spherical diameters predicted by the low-angle x-ray scattering data.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2805-2816 
    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 results of a study of irradiated and unirradiated samples of polymers prepared by plasma polymerization in an inductively coupled radiofrequency (rf) reactor using infrared, elemental, thermogravimetric, and ESR analyses and density and refractive index measurements are presented. The plasma-formed polymers studied include polypropylene, poly(ethylbenzene), poly(methyl methacrylate), poly(tetrafluoroethylene), poly(chlorotrifluoroethylene), and poly(trimethylchlorosilane).
    Additional Material: 5 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 669-676 
    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: Polyimidothioethers were synthesized as possible polymers for evaluation as X-ray resists. These polymers were varied in the ratio of the monomers and in their structures. Aliphatic thiols, bismaleimides, and iodonium monomers were used. The composition was varied using ratios of the bisimide to iodonium of 9: 1, 8 : 2, 7 : 3, 6 : 4, 5 : 5, and 0 : 1. The ratio of the thiols, containing 6 to 10 —CH2— groups, to the monomers was 1 : 1. The synthesis and characterization of the intermediate compounds and polymers are described in detail.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2089-2106 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(chloro-p-xylylene) was synthesized in a manner similar to poly(p-xylylene) using Gorham's method at various cryogenic temperatures. The effect of the sublimation rate of dimer on the kinetics of deposition, crystallinity, and crystalline structure was studied. Increasing the sublimation rate of the dimer increases the deposition rate similar to that of poly(p-xylylene). However, an increase in crystallinity, in contrast to Parylene N, is observed, although, in general, Parylene C has lower crystallinity relative to Parylene N. No polymorphism is observed either by decreasing the deposition temperature or by increasing the sublimation rate of the dimer. Solution annealing and isothermal annealing both bring about crystallization without any structural transformation. Solution annealing removes the oligomers and dimers, but no crystalline oligomers are ever detected under the scanning electron microscope (SEM). The surface topology of films synthesized from ambient temperature to -40°C is very similar to Parylene N. At lower temperatures, in the region -50 to -60°C, a rod-type morphology is observed similar to Parylene N. The surface topology of samples synthesized at -196°C is totally different from that of Parylene N. All low temperature synthesized samples are amorphous.
    Additional Material: 13 Ill.
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  • 8
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of the sublimation rate of di-p-xylylene on the crystallinity and morphology of Parylene N deposited on stainless steel was studied as a function of substrate temperature. For a given rate of dimer sublimation, the deposition rate increases with decreasing substrate temperature. Increasing the sublimation rate of the dimer increases the deposition rate 10-fold, decreases the crystallinity, and shifts the appearance of the hexagonal β structure towards higher substrate temperature for samples synthesized from room temperature (RT) to -60°C. Solution annealing resulting from solvent extraction, and isothermal annealing, increase the crystallinity of the polymers and result in structures containing both α and β polymorphs. The surface topology, as revealed by scanning electron microscopy (SEM), for polymers synthesized from RT to -40°C shows a globular structure, whereas low temperature samples exhibit a rod-type morphology. For higher sublimation rates of the dimer, SEM micrographs show that oligomeric species start appearing on the polymer films after a period of 4-5 days. Solvent extraction removes the oligomeric crystals, and GPC analysis of the resulting extract indicates that most of the oligomers range in molecular weight from 100 to 900. The cross-sectional morphology for fractured low temperature samples, however, reveals different morphologies as polymerization proceeds. It is postulated that in the temperature range -50 to -78°C, both surface condensation and surface adsorption of monomer occurs, leading to different morphologies and lower crystallinity. The polymer synthesized at liquid nitrogen temperature shows the presence of voids along with different morphologies. X-ray diffractograms of polymers synthesized at liquid nitrogen reveal a considerable amount of amorphous phase in the films. Hence, it is inferred that, although the liquid nitrogen polymerization is a solid state polymerization of the crystalline monomer, it does not lead to 100% crystalline material, and the reasons for this are discussed.
    Additional Material: 13 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 545-568 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polychloro-p-xylylene (Parylene C) and poly-p-xylylene (Parylene N) films were synthesized in vacuum with and without the presence of 42 mtorr of argon at various deposition temperatures and three different dimer sublimation rates. Depending on the synthesis conditions, the morphology of the films can vary from a homogeneous (nonporous) structure to a heterogeneous (porous) structure. The transport coefficients of the gases He, O2, N2, and CO2 through these films were measured at 25°C. The transport coefficients for both types of films vary with the deposition temperature and the dimer sublimation rate. The variation, however, cannot be solely explained by the change of crystallinity. Anomalous transport behavior is observed in the homogeneous, as-synthesized polymers of relatively high crystalline content (above 20-30%). In many cases the permeabilities and diffusivities increase despite an increase in crystallinity. The effects of crystallization induced by isothermal and solvent annealing on the transport coefficients of polymers of Parylene C are different from those of Parylene N synthesized with or without argon. The mean pore size and effective porosity of the porous films were calculated from gas permeation data. For Parylene C and Parylene N porous films synthesized without argon, increasing the dimer sublimation rate or decreasing the deposition temperature increases the mean pore size but decreases the effective porosity. For Parylene N porous films synthesized in the presence of argon, increasing the dimer sublimation rate or decreasing the deposition temperature results in a decrease in the mean pore size but an increase in the effective porosity. Overall, no appreciable change in transport coefficients is observed upon addition of an inert gas.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 23 (1985), S. 639-645 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 6 Ill.
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