1995
DOI: 10.1016/0032-3861(95)93119-7
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Preparation of oligoester diols by alcoholytic destruction of poly(ethylene terephthalate)

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Cited by 54 publications
(57 citation statements)
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“…The glycolysis reaction was carried out in a continuously stirred three-necked flask equipped with a condenser, thermometer and nitrogen inlet, in order to avoid the oxidation products obtained in presence of atmospheric oxygen and elevated temperature. The temperature of the reaction was kept constant at 200-220 8C for a time period of 4 h. [11][12][13][14][15] After the completion of glycolysis reaction, the product was cooled to room temperature, dissolved in a suitable amount of dichloromethane (CH 2 Cl 2 ), and shaken vigorously with an equal amount of distilled water in order to get rid of unreacted glycol and remaining catalyst. [16,17] After phase separation between the two layers, the organic layer (oligoesters dissolved in organic solvent) was collected and washed several times with distilled water.…”
Section: Synthesis Of Oligoester Polyolsmentioning
confidence: 99%
“…The glycolysis reaction was carried out in a continuously stirred three-necked flask equipped with a condenser, thermometer and nitrogen inlet, in order to avoid the oxidation products obtained in presence of atmospheric oxygen and elevated temperature. The temperature of the reaction was kept constant at 200-220 8C for a time period of 4 h. [11][12][13][14][15] After the completion of glycolysis reaction, the product was cooled to room temperature, dissolved in a suitable amount of dichloromethane (CH 2 Cl 2 ), and shaken vigorously with an equal amount of distilled water in order to get rid of unreacted glycol and remaining catalyst. [16,17] After phase separation between the two layers, the organic layer (oligoesters dissolved in organic solvent) was collected and washed several times with distilled water.…”
Section: Synthesis Of Oligoester Polyolsmentioning
confidence: 99%
“…This fact confirms that the molar ratio of DEG : PET plays an important role in determining the nature of the obtained gylcolysates. [24] Molecular weight determination Molecular weights of all synthesized unsaturated polyester resins (UP1-UP12) are determined by end-group analysis. [12] Each UP is analyzed for both acid number (A) and hydroxyl value (B) in mg KOH/g, and the numberaverage molecular weight M -n is then calculated from Eq.…”
Section: Resultsmentioning
confidence: 99%
“…Glycolysis reaction was carried out in a continuously stirred three-necked flask equipped with a condenser. The temperature of the reaction was kept constant at 200 -220 8C for a time of 4 h. [12][13][14][15][16] After completion of the glycolysis reaction, the product is cooled to room temperature, dissolved in a suitable amount of non-polar organic solvent, e. g., CH 2 Cl 2 , CCl 4 or benzene, and shaken vigorously with an equal amount of distilled water in order to get rid of unreacted glycol and remaining catalyst. [17] After phase separation between the two layers, the organic layer (oligomer dissolved in non-polar solvent) is collected and washed several times with distilled water by the same way.…”
Section: Experimental Partmentioning
confidence: 99%
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