Method for reducing N oxo-compound
A compound and oxygen technology, applied in the field of reducing N-oxyl compounds contained in easily polymerizable substances, can solve problems such as decreased stability and increased acid value
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Embodiment 1
[0042] 100 g of MMA containing 100 ppm of N-oxyl compound 8 and 0.5 g of activated clay Galeona-su GSF (manufactured by Mizusawa Chemical Industry Co., Ltd.) were added to a 300 ml four-necked flask, and stirred at room temperature for 60 minutes. The treated solution after stirring was filtered with a membrane filter (pore diameter: 0.5 μm) to obtain 98.7 g of MMA (98.7% recovery rate). The N-oxyl compound 8 contained in this MMA was below the quantitative limit (0.1 ppm).
Embodiment 2
[0044] The N-oxyl compound reduction treatment was carried out in the same manner as in Example 1, except that 100 g of MMA containing 20 ppm of the N-oxyl compound 1 was used as a polymerization inhibitor. The obtained MMA was 98 g (98% recovery), and the N-oxyl compound 1 contained therein was below the quantitative limit (0.1 ppm). Example 3
Embodiment 3
[0045] The N-oxyl compound reduction treatment was carried out in the same manner as in Example 1 except that 100 g of ethylene glycol dimethacrylate was used instead of MMA. The obtained ethylene glycol dimethacrylate was 98.5 g (98.5% recovery rate), and the N-oxyl compound 8 contained in it was below the quantitative limit (0.1 ppm).
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