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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2013 · IF 2.108

The dynamic interfacial adsorption and demulsification behaviors of novel amphiphilic dendrimers

Pei Zhang,Hui Wang,Xia Liu,Xuefeng Shi,Jian Zhang,Guang Yang,Keji Sun,Jinben Wang

The dynamic surface tension and dilational viscoelasticity properties of amphiphilic polyamidoamine (PAMAM) dendrimers were investigated to probe the hydrophobic chain effect on the interfacial properties and the demulsification behaviors. The values of dynamic parameters n and t * representing diffusion speed of the molecules obtained according to the Rosen equation decreased with the increasing of bulk concentration. Taking the hydrophobic effect into consideration, the t * values decreased and n values increased with the increase of alkyl chain length, suggesting easier adsorption and faster diffusion for longer hydrophobic chain which was opposite to the tendency of traditional surfactants. Further dilational viscoelasticity studies demonstrated that the properties referring to adsorption and exchange-diffusion were probably affected by the aggregates conformation at the interface. Subsequently, from the demulsification experiments a conclusion can be drawn that the amphiphilic dendrimers with branched dendritic structure possesses superior properties of breaking W/O crude oil emulsions, showing a certain correlation to the dilational viscoelasticity properties.

研究领域: 胶体与界面化学 · 石油化学 · 高分子科学 · 流变学 · 表面活性剂化学
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POLYMER DEGRADATION AND STABILITY · 2016 · IF 3.12

Synthesis of a novel macromolecular charring agent with free-radical quenching capability and its synergism in flame retardant polypropylene

Huali Xie,Xuejun Lai,Hongqiang Li,Xingrong Zeng

Fabricating an effective synergism between the condensed phase (char-forming) and the gas phase (free-radical quenching) is recently considered to be a very promising way to prepare high-efficient intumescent flame retardants . In this work, a novel hindered amine phosphorous-nitrogen macromolecular charring agent (HAPN) with free-radical quenching capability was synthesized and characterized. Then it was combined with ammonium polyphosphate (APP) to flame-retard polypropylene (PP). The flame retardancy and thermal stability of PP/HAPN/APP mixtures were investigated by limiting oxygen index (LOI), vertical burning test (UL-94), cone calorimetric test (CCT) and thermogravimetric analysis (TGA). When the content of HAPN/APP was 25 wt%, PP/HAPN/APP could self-extinguish at 36 s after igniting in the oxygen concentration of 29.5% and achieve a UL-94 V-0 rating. Meanwhile, the peak heat release rate (PHRR), total heat release rate (THR), average heat release rate (AV-HRR) and average mass loss rate (AV-MLR) were significantly decreased. The flame retardant mechanism of HAPN/APP was explored and the results revealed that there was an effective synergism between the condensed phase and the gas phase during the combustion. In the condensed phase, HAPN could make PP involve into the char-forming reaction to promote the formation of compact and firm intumescent char layer. Simultaneously, the nitroxyl radical generated by HAPN could effectively restrain and even extinguish the flame in the gas phase by quenching the active free-radicals.

研究领域: 高分子化学 · 材料科学 · 阻燃材料 · 热稳定性 · 燃烧性能
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2015 ·Vol. 54 ·期 3 ·368-380 · IF 3.113

Hyperbranched block copolymer from AB2 macromonomer: Synthesis and its reaction-induced microphase separation in epoxy thermosets

Jingang Li,Yixin Xiang,Sixun Zheng

In this contribution, we reported the synthesis of a hyperbranched block copolymer composed of poly(ε-caprolactone) (PCL) and polystyrene (PS) subchains. Toward this end, we first synthesized an α-alkynyl- and ω,ω′-diazido-terminated PCL- b -(PS) 2 macromonomer via the combination of ring-opening polymerization and atom transfer radical polymerization. By the use of this AB 2 macromonomer, the hyperbranched block copolymer ( h -[PCL- b -(PS) 2 ]) was synthesized via a copper-catalyzed Huisgen 1,3-dipolar cycloaddition (i.e., click reaction) polymerization. The hyperbranched block copolymer was characterized by means of 1 H nuclear magnetic resonance spectroscopy and gel permeation chromatography. Both differential scanning calorimetry and atomic force microscopy showed that the hyperbranched block copolymer was microphase-separated in bulk. While this hyperbranched block copolymer was incorporated into epoxy, the nanostructured thermosets were successfully obtained; the formation of the nanophases in epoxy followed reaction-induced microphase separation mechanism as evidenced by atomic force microscopy, small angle X-ray scattering, and dynamic mechanical thermal analysis. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 368–380

研究领域: 高分子化学 · 材料科学 · 纳米结构功能材料 · 聚合物自组装 · 热固性树脂改性
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