两亲扩展型共聚物的合成及中间极性嵌段对乳化性能的影响
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东华大学中央高校基本科研业务费专项资金(批准号:12D10521)


Synthesis of Amphiphilic Extended Copolymers and the Influence of Intermediate Polar Block on Emulsifying Properties
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    摘要:

    采用聚乙二醇单甲醚 (Mn=1900, 5000) 分别引发丙交酯和ε-己内酯开环聚合合成了中间嵌段(PLA)聚合度递增的聚乙二醇-聚丙交酯-聚己内酯 (PEG-PLA-PCL) 两亲扩展型共聚物和相应的聚乙二醇-聚己内酯 (PEG-PCL)两嵌段共聚物。用FT-IR、1H-NMR和GPC对产物结构进行了表征,研究了共聚物和常规低分子表面活性剂的乳化性能,探讨了中间极性嵌段的长度对共聚物乳化性能的影响。结果表明,对于甲苯/水体系,共聚物可用于制备稳定的O/W型乳液,且三嵌段共聚物的乳化性能优于低分子表面活性剂;随着引入PLA嵌段聚合度的增加,共聚物的乳化能力呈先增加后减小的趋势,这是由于引入的中间嵌段可增加共聚物与水相和油相的作用,使两相界面膜变厚;相对于PEG1900系列共聚物,PEG5000系列共聚物中需要引入更长的中间嵌段才能获得最佳乳化性能。

    Abstract:

    The amphiphilic triblock copolymer poly(ethylene glycol)-co-polylactide-co-poly(ε-caprolactone) (PEG-PLA-PCL) with increasing PLA block ratio and corresponding diblock copolymer poly(ethylene glycol)-co-poly(ε-caprolactone) (PEG-PCL)were prepared using ring-opening polymerization of d,l- lactide and ε- caprolactone initiated by monomethoxy poly(ethylene glycol)(Mn=1900, 5000). The structure of the target copolymers was confirmed by means of FT-IR,1H-NMR spectra and GPC, then emulsifying properties of the copolymers and low molecular surfactants were studied and their relationship with the block ratio of the intermediate polar block PLA in triblock copolymers was discussed in detail. The results indicate that all of the copolymers can emulsify the toluene/water system and the emulsions were oil-in-water type. The copolymers show better emulsifying properties than the low molecular surfactants, and the emulsifying ability of the copolymers first increased and then decreased with the increase of PLA block ratio. It is because that the interactions with water and oil phase are enhanced by inserting intermediate polar block PLA, leading to a thicker interfacial membrane. To achieve optimum emulsifying performance, longer intermediate polar block was required for PEG1900-containing copolymers than that for PEG5000-containing copolymers.

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宗秋艳,董霞,何瑾馨.两亲扩展型共聚物的合成及中间极性嵌段对乳化性能的影响[J].精细化工,2013,30(5):

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  • 收稿日期:2012-12-05
  • 最后修改日期:2013-01-31
  • 录用日期:2013-03-04
  • 在线发布日期: 2013-05-03
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