Method for preparing polylactic acid radiation grafting copolymer with electron accelerator
An electron accelerator and radiation grafting technology, which is applied in the field of preparation of radiation graft copolymers, can solve the problems of large loss of mechanical properties, large penetration depth, and changes in degradation rate of polylactic acid materials, and achieve good surface hydrophilicity and degradation rate, simplified modification process steps, and strong ray penetration
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Embodiment 1
[0029] Distill the N-vinylpyrrolidone under reduced pressure to remove the polymerization inhibitor, the vacuum degree is -0.095MPa, seal the N-vinylpyrrolidone from which the polymerization inhibitor has been removed, and place it in a desiccator for future use.
[0030] Measure 6ml of N-vinylpyrrolidone from which the polymerization inhibitor was removed, dissolve it in 14ml of methanol, and add 0.056ml of acetic acid to form a solution. Measure 11ml of the acetic acid methanol solution of N-vinylpyrrolidone, pour it into the cell culture bottle, then weigh 0.2004g of polylactic acid and put it into the cell culture bottle, and make it completely soaked in the acetic acid methanol solution of N-vinylpyrrolidone middle. Vacuumize and fill with nitrogen repeatedly for 5 times, and finally seal the tube with nitrogen. The sealed tube sample is sent to the accelerator for irradiation, the velocity flow of the accelerator is 2 mA, and the absorbed dose is 2 kGy.
[0031] Take o...
Embodiment 2
[0034] Distill the N-vinylpyrrolidone under reduced pressure to remove the polymerization inhibitor, the vacuum degree is -0.095MPa, seal the N-vinylpyrrolidone from which the polymerization inhibitor has been removed, and put it in a desiccator for future use.
[0035] Measure 6ml of N-vinylpyrrolidone from which the polymerization inhibitor was removed, dissolve it in 14ml of methanol, and add 0.056ml of acetic acid to form a solution. Measure 11ml of the acetic acid methanol solution of N-vinylpyrrolidone, pour it into the cell culture bottle, then weigh 0.2222g of polylactic acid and put it into the cell culture bottle, and make it completely soaked in the acetic acid methanol solution of N-vinylpyrrolidone middle. Vacuumize and fill with nitrogen repeatedly for 5 times, and finally seal the tube with nitrogen. The sealed tube sample is sent to the accelerator for irradiation, the velocity flow of the accelerator is 2 mA, and the absorbed dose is 4 kGy.
[0036] Take out...
Embodiment 3
[0039] Distill the N-vinylpyrrolidone under reduced pressure to remove the polymerization inhibitor, the vacuum degree is -0.095MPa, seal the N-vinylpyrrolidone from which the polymerization inhibitor has been removed, and place it in a desiccator for future use.
[0040] Measure 6ml of N-vinylpyrrolidone from which the polymerization inhibitor was removed, and dissolve it in 14ml of methanol to form a solution. Measure 11ml of the methanol solution of N-vinylpyrrolidone, pour it into the cell culture bottle, then weigh 0.2084g of polylactic acid and put it into the cell culture bottle, and make it completely immersed in the methanol solution of N-vinylpyrrolidone in acetate . Vacuumize and fill with nitrogen repeatedly for 5 times, and finally seal the tube with nitrogen. The sealed tube sample is sent to the accelerator for irradiation, the velocity flow of the accelerator is 4 mA, and the absorbed dose is 8 kGy.
[0041] Take out the irradiated sample, wash the surface of...
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