کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
594878 1453991 2011 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis, surface and aggregation properties of glucosamide-grafted amphiphilic glycopolysiloxanes
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Synthesis, surface and aggregation properties of glucosamide-grafted amphiphilic glycopolysiloxanes
چکیده انگلیسی

Three glucosamide-grafted amphiphilic glycopolysiloxanes (APFPS-GL) were synthesized through a two-step method. First, the aminopropyl functional polysiloxanes (APFPS) were synthesized by equilibrium polymerization; then, gluconolactone was conjugated to the APFPS via ring-opening reaction to give the glycopolysiloxanes APFPS-GL. The final compositions of the amphiphilic glycopolysiloxanes were characterized by FT-IR, 1H NMR and 13C NMR. Surface activities and aggregation behavior in aqueous solution of these three glycopolysiloxanes were investigated by surface tension measurements, dynamic light scattering (DLS) and transmission electron microscopy (TEM). The results show that these three glycopolysiloxanes have much higher surface activity than those of conventional carbon–carbon chain glycopolymers in aqueous solution and they can self-assemble into spherical micelles with average diameters in the range from 200 to 600 nm.

Amphiphilic glycopolysiloxanes which have high surface activity were synthesized.Figure optionsDownload as PowerPoint slideHighlights
► Three novel amphiphilic glycopolysiloxanes were synthesized by two-step reactions.
► The amphiphilic glycopolysiloxanes can reduce surface tension of water to much lower values compared with the carbon–carbon chain amphiphilic glycopolymers.
► The amphiphilic glycopolysiloxanes can self-assemble into polymeric micelles with wide rang in diameters.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Colloids and Surfaces A: Physicochemical and Engineering Aspects - Volume 381, Issues 1–3, 20 May 2011, Pages 55–60
نویسندگان
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