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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1459-1470 
    ISSN: 0887-6266
    Keywords: Polyacrylonitrile ; propylene carbonate ; thermoreversible gels ; NMR ; x-ray ; lattice expansion ; solvated crystallites ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of thermoreversible polyacrylonitrile-propylene carbonate (PAN-PC) gels was examined using solid-state carbon-13 nuclear magnetic resonance (NMR) spectroscopy and x-ray diffraction. Following complete dissolution of the polymer at elevated temperature and cooling of the concentrated PAN-PC solutions, a gel was formed. The PAN-PC gels consisted of regions of mobile polymer chains, rich in PC, “cross-linked” by regions of rigid polymer. The mobile regions of the gels showed solution-type NMR spectra with resolution of tacticity effects. The rigid component detected by NMR would correspond to the crysttallites detected previously by x-ray diffraction. Wide-angle x-ray diffractograms of the gels showed different peaks when compared with the dry polymer powder. After solvent extraction and drying of the gel, the diffractogram reverted to that of the original dry powder. This new result is the strongest evidence to support the view advanced earlier that the new peaks found in the diffraction pattern of the wet gels arises from solvated polymer crystallites rather than from ordinary polymer crystallites. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 1509-1516 
    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 synthesis and characterization of aromatic copolyesters containing terephthalic acid and phenyl hydroquinone as the major constituents and either 1,4-napthalene diol or 1,4-anthracene diol as the minority comonomer is described. Both polymers melted in the vicinity of 300°C, giving birefringent fluids. Optical microscopy showed Schlieren textures consisting predominantly of inversion walls characteristic of the nematic phase. The clearing temperature was in the vicinity of 460°C, but was accompanied by charring. DSC experiments showed a high glass transition temperature of 130-160°C for both polymers. Crystalnematic and nematic-isotropic endotherms were observed on heating; however, degradation took place near the isotropization temperature. Thus, on cooling, the sequence was reversible only if the previous heating was beyond the crystal-nematic but below the isotropization temperature. The polymers were stable in terms of gross weight loss until about 450°C, though there were indications that crosslinking occurred above about 400°C over a short period of time. The polymers formed low-viscosity injection-molding compounds, but to use them effectively, it would require mold-gate designs that reduce the “jetting” tendency for liquid crystal polymer melts, which result in weld lines. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 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. 1957-1967 
    ISSN: 0887-6266
    Keywords: liquid crystals ; polyesters ; smectic mesophase ; crystallization ; optical textures ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This work reports the phase behavior of the polyesters made from the condensation of isophthalic acid (IA) and terephthalic acid (TA) with the mesogenic diol 4,4′-bis (6-hydroxy hexoxy) biphenyl (BHHBP). The latter monomer forms a smectic mesophase in the interval 98-179°C. Fischer et al., who investigated the room temperature x-ray patterns of the oriented polyesters of BHHBP and IA, as well as BHHBP and TA, claimed that both polymers also showed smectic mesophases. However, they showed no other evidence to support their interpretation. In the present work, examination of these polyesters under the optical microscope revealed focal conic textures for the IA polyester, but spherulitic textures for the TA polyester. DSC studies revealed thermograms with two peaks in the cooling scan for the IA polyester, at different cooling rates, which supported the view that there were two phase transitions. The heating scans of the TA polyester showed multiple peaks that depended on heating rate whereas on cooling, only a single exothermic peak was observed at all cooling rates. Thus, the current results definitely support the case for a smectic A mesophase in the IA polyester but, contrary to Fischer et al.'s opinion, do not suggest any mesophase formation in the TA polyester. © 1995 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2077-2084 
    ISSN: 0887-6266
    Keywords: liquid crystals ; polyesters ; nematic-smectic biphase ; monotropic ; crystallization ; optical textures ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polyesters made from the condensation of isophthalic acid (IA) or terephthalic acid (TA) with the mesogenic diol 4,4′-bis (6-hydroxy hexoxy)biphenyl (BHHBP) are both reported to show a smectic mesophase. However, in our previous work, we found evidence for a mesophase in the polyester containing BHHBP and IA, but not in the one with BHHBP and TA. For the BHHBP-IA polyester, we thought the phase sequence on cooling was I → SA → K, while on heating the situation was unresolved; there was some indication that on heating, a K → I transition occurs without any intervening mesophase. In other words, it was suspected that the mesophase in the IA polyester was monotropic. In this work, we have now obtained firm evidence that the mesophase behavior of the BHHBP-IA polyester is indeed monotropic. Further, an additional complexity has been found: on cooling, there is in fact a nematic phase, besides a smectic A, and a crystal phase. However, the mesophase appears to be complex. As the nematic and smectic textures occurred simultaneously, it seems that the mesophase is a nematic-smectic biphase. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 33 (1994), S. 9-17 
    ISSN: 0959-8103
    Keywords: Polyacrylonitrile ; infrared dichroism ; orientation factors ; X-ray ; laterally-ordering ; solvent orientation ; dipole pairing ; 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: Polyacrylonitrile (PAN) films were made by casting a dimethyl sulphoxide (DMSO) solution. After drying, the films were uniaxially drawn by an essentially solid-state drawing procedure. Using polarised-infrared (IR) spectroscopy, the dichroism of the nitrile-stretching vibration was monitored as a function of draw ratio. The dichroism results were converted to plots of chain-orientation factor versus draw ratio. For this, α, the transition-moment angle of the vibration, has to be known. Though a value of 68-73° has been suggested in the literature, for the present samples α cannot be 70° or less, and 73° is the most appropriate. The meaning and nature of the transition-moment angle in the context of a flexible-chain polymer molecule is discussed. The IR spectrum also showed dichroism in the S=O stretch and the —CH3 rocking vibrations from the (residual) DMSO present in the film, indicating that the solvent molecules were also orientated. It is proposed that this occurred due to dipolar interactions between the S=O and the C≡N groups, which led to solvent molecules being bound to the polymer chains. X-ray diffraction studies indicated ‘lateral-ordering’ consisting of hexagonally packed, rod-like chains with no c-axis order. The diffraction patterns obtained here were the ‘standard’ ones for PAN, in contrast to those observed previously in solvent-containing PAN gels.
    Additional Material: 6 Ill.
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  • 6
    Publication Date: 2019-12-09
    Description: The 3D printing of articles by the effect of a directed laser beam on a plastic powder is a demanding process, and unlike injection molding, very few polymers work well enough with it. Recently, we reported that poly(ethylene terephthalate) (PET) powder has intrinsically good properties for 3D printing. Basic mechanical properties were shown earlier and it was demonstrated that unfused but heat-exposed PET powder does not degrade quickly allowing good re-use potential. In this work, we conducted a detailed comparison of the mechanical properties of PET and polyamide 12 from different build orientations. PET powders with two different molecular weights were used. With the high molecular weight powder, the processing parameters were optimized, and the printed bars showed little difference between the different orientations, which means there is low anisotropy in mechanical properties of built parts. Based on processing experience of the first powder, the second powder with a lower molecular weight was also very printable and complex parts were made with ease from the initial printing trials; since the process parameters were not optimized then, lower mechanical properties were obtained. While the intrinsic material properties of PET (melting and re-crystallization kinetics) are not the best for injection molding, PET is eminently suitable for powder bed fusion.
    Electronic ISSN: 2073-4360
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
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  • 7
    Publication Date: 2020-09-08
    Description: Metal-plastic composites have the potential to combine enhanced electrical and thermal conductivity with a lower density than a pure metal. The drawback has often been brittleness and low impact resistance caused by weak adhesion between the metal filler and the plastic. Based on our observation that aluminum foil sticks very strongly to poly(ethylene terephthalate) (PET) if it is used as a backing during compression moulding, this work set out to explore PET filled with a micro and a nano aluminum (Al) powder. In line with other composites using filler particles with low aspect-ratio, the tensile modulus increased somewhat with loading. However, unlike most particle composites, the strength did not decrease and most surprisingly, the Izod impact resistance increased, and in fact more than doubled with certain compositions. Thus, the Al particles acted as a toughening agent without decreasing the modulus and strength. This would be the first case where addition of a metal powder to a plastic increased the modulus and impact resistance simultaneously. The Al particles also acted as nucleating agents but it was not sufficient to make PET crystallize as fast as the injection moulding polyester, poly(butylene terephthalate) (PBT).
    Electronic ISSN: 2073-4360
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
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