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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1875-1882 
    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 chemical structure of polyurethane modified by BHET is correlated with its mechanical and dynamic mechanical properties. Evaluation of this amorphous elastomer by means of stress-strain tests and transition temperature measurements reveals that incorporation of the BHET structure into the soft polyester segment affects the domain structure and, in turn, the entire mechanical behavior of polyurethane. It is also shown that polyurethane has a wide range of Tg and secondary transition temperature by varying the ratio of BHET to EG as well as the ratio of TDI to polyester polyol.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Particle and Particle Systems Characterization 4 (1987), S. 78-82 
    ISSN: 0934-0866
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An evaluation was made to assess whether linear grade distribution measurements determined from polished sections of randomly oriented particles can be used to estimate the extent of liberation for multiphase particles of specified size. Two techniques, optical image analysis and microprobe analysis, were used to establish the linear grade distributions for samples of different composition from a copper porphyry flotation circuit and these two were found to be equivalent. An estimate of the variance in the experimental data was made by measuring the average chalcopyrite content in these samples and comparing the results to chemical assays. The statistical significance of the linear grade distribution data obtained by optical image analysis was assessed and, for a given accuracy, the number of particles required to obtain an unbiased representation of the sample was determined.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1803-1811 
    ISSN: 0887-6266
    Keywords: ramp rate ; polyimide ; bending-beam technique ; stress ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stress in films of semirigid and rigid polyimides (PIs) on silicon (Si) substrate has been measured in situ during curing using a newly modified bending beam apparatus. By using the apparatus, the onset of residual stress in the initially solvent-rich films has also been investigated. The stress characteristics of the PI films are strongly ramp rate dependent. Different ramp rates result in markedly different stress patterns, thermo-mechanical properties, and film morphologies. The residual stress at room temperature after curing is scattered around 23-31 MPa for the films of pyromellitic dianhydride-4,4′-oxydianiline (PMDA-ODA). For pyromellitic dianhydride-p-phenylenediamine (PMDA-PDA), it systematically increases from -6 to 28 MPa for ramp rate increasing from 0.5 to 10°C/min. The residual stress is very low in the slowly cured PMDA-PDA films. However, these films have gone through a very high-stress transient state during curing. The maximum transient stress is comparatively higher in the films of PMDA-PDA than in PMDA-ODA. Slowly cured PMDA-PDA films exhibit high structural ordering, high in-plane anisotropy, and low coefficient of thermal expansion. ©1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 2239-2242 
    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: Bis-maleimide (BMI) has recently attracted condsiderable attention as an important matrix resin for high-performance composites, due to its outstanding high-temperature performance. First-generation BMI is too brittle for primary strauture. Our toughening approach began by dissolving PEI (polyetherimide) into compatible dially compound (Matrimid 5292 B, Ciba Geigy) prior to coreaction with BMI resin. In this note, the toughness and interface properties were investigated for the toughened matrix system.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1233-1241 
    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 co[poly(ethylene terephthalate-p-oxybenzoate)] thermotropic copolyester was synthesized from various ratios of two different moieties of either poly(ethylene terephthalate) (PET) or its oligomer as moiety (II) with p-acetoxybenzoic acid as moiety (I) through the polycondensation process. The polymeric products obtained were then ground and subjected to solid-state polymerization under vacuum for various polymerization times. Thermogravimetric analysis (TGA) and the derivative thermogravimetric analysis (DTG) were performed with these samples obtained. Also, a commercial product, Eastman 10109, was analyzed in comparison with these samples. It was found that the copolyesters made of PET and of its oligomer in a p-oxybenzoate (POB):PET = 80 : 20 composition ratio and subjected to 8 and 4 h solid-state polymerization times, respectively, showed the most similar thermogravimetric behavior with Eastman 10109. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1727-1734 
    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 co[poly(ethylene terephthalate-p-oxybenzoate)] thermotropic copolyesters with various compositions were prepared by the copolymerization of either poly(ethylene terephthalate) polymer (PET) or its oligomer (OET) as moiety (II) and p-acetoxy-benzoic acid (POB) as moiety (I). The polymeric products obtained were then subjected to solid-state polymerization. The glass and melting transitions of the copolyesters obtained have been studied by differential scanning calorimetry (DSC). Effects of composition and solid-state polymerization on DSC are discussed. The melting point of copolyesters possesses a higher value if the PET polymer is used as PET moiety in the copolyesters. In the DSC scan of the POB rich composition, the endothermic peak shows obscurely and enthalpy of fusion becomes small due to the change in the crystalline morphology from isotropic to anisotropic. In general, the melting point of copolyesters is increased by the solid-state polymerization reaction. It is also found that both the melting temperature and enthalpy of fusion of the copolyesters can be increased simultaneously by the solid-state polymerization reaction only when the composition of POB/PET is 80/20. This phenomenum at this composition may be attributed to the annealing effect caused by the randomness of two moiety units on the backbone chain of copolyesters and the increased molecular weight as well. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 869-873 
    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: Polyurethanes were synthesized from polyester polyols, derived from PET Waste. The PET waste was first depolymerized by glycolysis. The glycolysized products were reacted with adipic acid to yield polyester polyols, and the polyester polyols were then reacted with either MDI or TDI to obtain polyurethanes. In this article, the thermal properties of the polyurethanes obtained are discussed in detail. © 1994 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1223-1231 
    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 dynamic and isothermal crystallization behaviors of polyethylene terephthalate (PET) blended with two types of co[poly(ethylene terephthalate-p-oxybenzoate)] copolyesters with different compositions, i.e., POB/PET = 20/80 (P28) and POB/PET = 80/20 (P82), has been studied by using differential scanning calorimetry (DSC). Both of these copolyesters in 10 wt % increase crystallization rate of PET in a manner similar to that of a nucleating agent. It is found that sample P28, which is an isotropic copolyester, accelerates the crystallization rate more significantly than that of P82, which is a thermotropic copolyester. The Avrami exponents n and rate constants k of these samples based on DSC studies were obtained in order to discuss the crystallization kinetics of PET accelerated by these copolyesters. The crystallization rate of the blends is also increased by 8 min blending due to the increased uniformity of the copolyester dispersed in the PET matrix. © 1994 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 1107-1112 
    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) (PET) was blended with four different kinds of co[poly(ethylene terephthalate-p-oxybenzoate)] copolyesters, designated P28, P46, P64, and P82, with the level of copolyester varing from 1 to 15 wt %. All samples were prepared by melt-mixing in a Brabender Plasticorder for 8 min. The crystallization behavior of samples were then studied via DSC. The results indicate that these four copolyesters accelerate the crystallization rate of PET in a manner similar to that of a nucleating agent. The acceleration of the PET crystallization rate was most pronounced in the PET/P28 blends with a maximum level at 10 wt % of P28, and in the PET/P28 blends, at 5 wt % of P82. The melting endotherm onset temperatures and the melting peak widths for the blends are comparable with those of neat PET. These results imply that the stability of PET crystalline phase in the blends does not change by blending. The observed changes in crystallization behavior, however, are explained by the effect of the physical state of the copolyester during PET crystallization as well as the content of the p-oxybenzoate (POB) moiety in corporated into the blends. © 1995 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 1447-1454 
    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) (PET) has been melt-mixed at 293°C with two types of co[poly(ethylene terephthalate-p-oxybenzoate) (POB-PET) copolyester, designated as P28 and P82, at the level of 10 wt %. The different p-acetoxybenzoic acid/PET mole ratios are 20/80 in P28 and 80/20 in P82. The blends were heated to 305°C and then cooled to 25°C at rate of 10°C/min. The crystalline morphology of these blends in the range from 25°C to 305°C is monitored by polarized light microscopy. Morphologic observations revealed a quicker appearance of crystalline in the blends upon the addition of 10 wt % copolyester as a nucleating agent. It is found that P28, which contains fewer POB units, is much more advantageous to the nucleation process than P82, which contains more POB units. According to the optical photomicrographs, sufficient uniformity of distribution of copolyester domains in the PET matrix is reached after 8 min blending. © 1996 John Wiley & Sons, Inc.
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