水溶液
Zeta电位
热分解
聚氨酯
反离子
高分子化学
化学
聚丙烯乙二醇
分解
环氧氯丙烷
三乙胺
粒径
核化学
材料科学
有机化学
纳米颗粒
物理化学
离子
聚乙二醇
纳米技术
作者
Yun Chen,Yun Chen,Yueh‐Liang Chen,Yueh‐Liang Chen
标识
DOI:10.1002/app.1992.070460308
摘要
Abstract The influence of counterions on the properties of aqueous dispersions of polyurethane (PU) anionomer have been investigated. The PU anionomers were prepared by polyaddition reaction of 4,4′‐methylenebis(phenylisocyanate) with poly(propylene glycol) (PPG), dimethylolpropionic acid (DMPA), and 1,4‐butanediol, followed by neutralization of pendant COOH groups by various bases. Stable dispersions are obtained for PU anionomers containing 0.8–1.1 wt % COOH groups (17.8–24.4 mmol/100 g polymer) that have been neutralized by ammonia, trimethylamine, triethylamine, LiOH, NaOH, and KOH, respectively. It is found that average particle size is determined mainly by the zeta potential of the dispersions. The number‐average diameter of the dispersions containing metal cations (Li‐, Na‐, and K‐0.9) is between 60–73 nm (zetal potential −65 to −70 mV), while that of the dispersions containing ammonium cations (AMM‐, TMA‐, and TEA‐0.9) is between 104–251 nm (zeta potential −47 to −64 mV). The surface tension of the dispersions decreases with concentration rapidly and levels off at concentrations higher than 20 mmol/L. The decreased decomposition temperature of the PU anionomers, compared to unionized PUs, can be attributed to the disordering of hard domains after ionization or decomposition reaction catalyzed by alkali metal carboxylates. The thermal decomposition proceeds mainly via cyclic elimination.
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