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  • DEG  (2)
  • 2,6-naphthalene dicarboxylic acid  (1)
  • Diglycidyl ether  (1)
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  • 1
    ISSN: 1572-8935
    Keywords: Diglycidyl ether ; Phosphorus-containing epoxy resin ; Char yield ; Limiting oxygen index ; Flame-retardant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract A novel aryl phosphinate diglycidyl ether, 10-(2′,5′-diglycidyl ether phenyl)-9,10-dihydro-9-oxa-l0-phosphaphenanthrene-10-oxide (DHQEP), was synthesized. The structure of the diglycidyl ether was characterized by elemental analysis, mass, FTIR, 1H, 13C, 31P NMR spectroscopies and X-ray single crystal analysis. In addition, compositions of the diglycidyl ether with three curing agents, e.g. phthalic anhydride (PA), hexahydrophthalic anhydride (HHPA), and aryl phosphinate anhydride (DMSA), were used for making a comparison of its heat and flame retardancy with that of DER331 and DEN438. The resulting aryl phosphinate epoxy-resin composites demonstrated a higher limiting oxygen index (LOT) value as well as a higher char yield, confirming the effectiveness of aryl phosphinate epoxide as a flame retardant for epoxy resins.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 3073-3080 
    ISSN: 0887-624X
    Keywords: direct esterification ; BHET ; EG ; DEG ; OH reactivity ; kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For revealing diethylene glycol (DEG) formation in poly(ethylene terephthalate) (PET) synthesis, this research focused on finding the stage most critical for DEG formation. It is found that the esterification stage was the most critical stage for DEG formation during production of PET through the direct esterification process. In addition, the kinetics of the formation of DEG (ether bond), which is mainly produced from hydroxyl end groups of ethylene glycol (EG) and bis-hydroxyethyl terephthalate (BHET) oligomer, was investigated. The results show that the reactivity of BHET-OH functional group is greater than that of EG-OH functional group in the reaction to produce ether bonds. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 3073-3080, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 3081-3087 
    ISSN: 0887-624X
    Keywords: TPA ; mol ratio ; DEG ; kinetics ; protons ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This research focused on studies of the effect of terephthalic acid (TPA) addition at the initial feed on diethylene glycol formation (DEG) in the process of polyethylene terephthalate (PET) preparation. Experimental results show that, when the mol ratio of ethylene glycol (EG) with TPA ranges from 1.0 to 1.3, the greater the amount of TPA added at the initial feed, the more DEG formed, and the greater the suppression of the rate of esterification and polymerization. In addition, the kinetics of EG with protons in the etherification reaction was considered in the study. It is found that, during the etherification reaction, the reactivity of hydroxyl end groups with ether bonds is higher than that of hydroxyl end groups on their own, and the activation energy of EG with protons is much lower than that of pure EG on its own. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 3081-3087, 1998
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 40 (1996), S. 93-98 
    ISSN: 0959-8103
    Keywords: phosphorus pentoxide/methanesulphonic acid ; polynaphthimidazoles ; 2,6-naphthalene dicarboxylic acid ; dimethyl 2,6-naphthalene dicarboxylate ; thermal stability ; 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: Phosphorus pentoxide/methanesulphonic acid (PPMA) was used as both solvent and condensing agent for the preparation of polynaphthimidazoles (PNIs) through direct polycondensation. The reactions of 2,6-naphthalene dicarboxylic acid and dimethyl 2,6-naphthalene dicarboxylate with tetramine monomer were studied with varying concentration of monomer, reaction temperature and reaction time in order to obtain high-molecular-weight polymer with high conversion. The properties, including solvent resistance, thermal properties and film casting, of synthesized polymers were also investigated. It was found that, using PPMA as both solvent and condensing agent, PNIs can be prepared successfully with high molecular weight by direct polycondensation of 2,6-naphthalene dicarboxylic acid or its derivatives with tetramine. The PNIs had inherent viscosities in the range 0.94-2.38 dl/g (in conc. H2SO4 at 30°C); however, polymers synthesized from isophthalic and terephthalic acids with tetramine had inherent viscosities of only 0.56dl/g and 0.48dl/g, respectively, with low conversions under similar reaction conditions. The glass transition temperature of the PNI 1 was 403°C. Thermal analysis indicates that these PNIs have excellent thermal stability, and the 10 wt% loss temperatures were recorded in the range 588-648°C in nitrogen gas, 533-580°C in air. The chemical stability and mechanical properties of films are also outstanding.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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