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  • 1
    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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  • 2
    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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