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酯交换法合成了一系列不同PEG含量的PET-PEG嵌段共聚物,并以差示扫描量热法研究了这些嵌段共聚物及纯PET的热性能。用毛细管流变仪研究了不同温度和不同长径比条件下它们的流为性能。 相似文献
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Aracely Serrano-Medina Irasema Oroz-Parra Victor E. Gomez-Resendiz Alexei Licea-Navarro 《国际聚合物材料杂志》2018,67(1):20-26
Temperature- and pH-sensitive core–shell nanogels were prepared by one-pot soapless emulsion polymerization of N-isopropylacrylamide and 2-methacryloyloxy benzoic acid with the aid of a crosslinker (core) using poly(ethylene glycol) methyl ether methacrylate as stabilizer (shell). The size of nanogels depended on the crosslinker used, being considerable smaller (around 100?nm) with the use of the acid-labile crosslinker 9-divinyl-2,4,8,10-tetraoxaspiro[5.5]-undecane (DVA). Doxorubicine (DOX) was loaded in nanogels with good efficiency. The empty nanogels were biocompatible for a lung cancer cell line (NCI-H1437), while the DOX-loaded, DVA-crosslinked nanogels resulted with efficient cytotoxicity for that cell line. 相似文献
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A novel and effective chain-extension procedure for obtaining high-molecular-weight PLGA-based bioerodible polymers is described. This procedure consists in a polycondensation reaction between PLGA thermal oligomers of average molecular weight 1000–3000 and bischlorofomates of either simple diols or α,ω-bis-hydroxylated oligomers, such as polyethyleneglycols or bis-hydroxy terminated poly-ε-caprolactones. In the latter case, multiblock copolymers are obtained. By varying the nature and the length of the starting diol, as well as the lactic/glycolic acid molar ratio in the starting PLGA oligomer, products with widely different physicochemical properties can be synthesized. In particular, dissolution times in aqueous media can be tuned within an ample range, from a few days to several months. This provides exceptional opportunities for designing products whose properties are tailored in view of specific applications in the biomedical field. © 1998 SCI. 相似文献
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Ananta Kumar MishraSaswata Bose Tapas KuilaNam Hoon Kim Joong Hee Lee 《Progress in Polymer Science》2012,37(6):842-869
Proton-exchange membrane fuel cells have emerged as a promising emission free technology to fulfill the existing power requirements of the 21st century. Nafion® is the most widely accepted and commercialized membrane to date and possesses excellent electrochemical properties below 80 °C, under highly humidified conditions. However, a decrease in the proton conductivity of Nafion® above 80 °C and lower humidity along with high membrane cost has prompted the development of new membranes and techniques. Addition of inorganic fillers, especially silicate-based nanomaterials, to the polymer membrane was utilized to partially overcome the aforementioned limitations. This is because of the lower cost, easy availability, high hydrophilicity and higher thermal stability of the inorganic silicates. Addition of silicates to the polymer membrane has also improved the mechanical, thermal and barrier properties, along with water uptake of the composite membranes, resulting in superior performance at higher temperature compared to that of the virgin membrane. However, the degrees of dispersion and interaction between the organic polymer and inorganic silicates play vital roles in improving the key properties of the membranes. Hence, different techniques and solvent media were used to improve the degrees of nanofiller dispersion and the physico-chemical properties of the membranes. This review focuses mainly on the techniques of silicate-based nanocomposite fabrication and the resulting impact on the membrane properties. 相似文献
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