水解
异佛尔酮二异氰酸酯
异佛尔酮
化学
聚氨酯
丁二醇
催化作用
高分子化学
有机化学
六亚甲基二异氰酸酯
二醇
发酵
作者
Suguru Motokucho,Yu Nakayama,Hiroshi Morikawa,Hisayuki Nakatani
摘要
ABSTRACT In order to develop a chemical recycling system of polyurethanes (PUs), environment‐friendly hydrolysis of two types of aliphatic PUs was studied under pressured CO 2 in water, in which the carbonic acid generated from CO 2 acted as an acid catalyst. Two PUs, namely H‐PU or I‐PU, were synthesized starting from 1,4‐butanediol and 1,6‐hexamethylene diisocyanate or isophorone diisocyanate, respectively. The hydrolysis of PUs depended on the experimental conditions, such as the temperature and CO 2 pressure. As a result, 98% of H‐PU and 91% of I‐PU were successfully hydrolyzed under the typical conditions of 190 °C for 24 h at 8.0 MPa CO 2 . The reaction mixtures afforded 1,4‐butanediol and diamines without the formation of any byproducts. Both of these raw materials generated from the originated PUs by selective hydrolytic cleavage of the urethane linkages, and they were easily isolated in high yields simply by evaporation of the water‐soluble components within the reaction mixture. By comparing the results of the two aliphatic PUs with those of an aromatic PU (M‐PU), the hydrolyzability was found to decrease in the order H‐PU, I‐PU, and M‐PU. The difference can be ascribed to the hydrophilicity of the aliphatic or aromatic groups connected to the urethane moieties at the terminals of PUs. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 45897.
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