A kind of modified polyethylene terephthalate and preparation method thereof
A kind of technology of ethylene glycol phthalate and terephthalic acid, which is applied in the field of preparation of modified polyethylene terephthalate, can solve problems such as reducing the viscosity of polyethylene terephthalate, To achieve the effect of not reducing molecular weight, increasing crystallinity, and increasing crystallization temperature
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[0015] The invention provides a preparation method of modified polyethylene terephthalate, comprising: (1) reacting ethylene glycol, terephthalic acid and a crystallization accelerator in the presence of an esterification catalyst to obtain a reaction product; 2) remove unreacted ethylene glycol from the reaction product, and then carry out polycondensation under polycondensation reaction conditions; the crystallization accelerator contains the structural unit shown in formula (1) and the structure shown in formula (2) A random copolymer of units,
[0016]
[0017] Among them, in formula (1) R 1 for C 2 -C 15 The content of the alkylene group represented by the formula (1) in the crystallization accelerator is 1-10 mol%.
[0018] The inventors of the present invention have found in research that in the esterification reaction of polyethylene terephthalate, the random copolymer containing the structural unit shown in formula (1) and the structural unit shown in formula (2...
preparation example 1
[0054] Synthesis of Crystallization Accelerator Poly(4-methyl-1-pentene-co-9-decen-1-ol)
[0055] The dry 100ml polymerization bottle was vacuumized and flushed three times with nitrogen repeatedly. At 25°C, start stirring, add 3.0ml of 4-methyl-1-pentene, 0.5ml of 9-decen-1-ol, 12.0ml of methylaluminoxane toluene solution in the polymerization bottle Each ml of methylalumoxane toluene solution contains 1.67mmol of methylalumoxane), and 1.0ml contains 50 μmol of dimethylsiloxane bis(2-methyl-indenyl)zirconium dichloride (purchased from STREM company) The toluene solution, and then start timing to carry out the copolymerization reaction at a temperature of 50° C. and a gauge pressure of 0.1 MPa for 6 hours. Stop stirring, carefully pour the reaction solution into a beaker, add acidified ethanol, stir for more than 6 hours, and filter to obtain the polymer. The polymer was vacuum dried at 60°C for 24 hours to obtain the product.
[0056] This copolymer is denoted as J-1, carr...
preparation example 2
[0058] Synthesis of Crystallization Accelerator Poly(4-methyl-1-pentene-co-9-decen-1-ol)
[0059] The dry 100ml polymerization bottle was vacuumized and flushed three times with nitrogen repeatedly. At 25°C, start stirring, add 3.0ml of 4-methyl-1-pentene, 0.1ml of 9-decen-1-ol, 12.0ml of methylaluminoxane toluene solution in the polymerization bottle Containing methylaluminoxane in every ml methylaluminoxane toluene solution is 1.67mmol), 1.0ml contains the toluene solution of 50 μ mol dimethylsiloxane bis(2-methyl-indenyl) zirconium dichloride, and then start Timely carry out the copolymerization reaction at a temperature of 40°C and a gauge pressure of 0.15 MPa for 4 hours. Stop stirring, carefully pour the reaction solution into a beaker, add acidified ethanol, stir for more than 6 hours, and filter to obtain the polymer. The polymer was vacuum dried at 60°C for 24 hours to obtain the product.
[0060] This copolymer is denoted as J-2, carries out GPC and 13 As measure...
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