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Effect of the Additionof a Cross-Linker and the WaterpH on the Physical Properties of Films of pH-Responsive Polymer Particlesat Air/Water Interfaces

机译:加法的效果交联剂与水pH值对pH响应型聚合物颗粒薄膜物理性能的影响在空气/水接口处

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摘要

We investigated how the stiffness and physical properties of films of pH-responsive polystyrene nanoparticles with poly(2-(N,N-dimethylamino)ethylmethacrylate) hairs (PDMA–PS particles) at air/water interfaces could be varied by using the cross-linker of 1,2-bis-(2-iodoethoxy)ethane (BIEE) and by varying the water pH. The physical properties of the film were investigated by using a Langmuir trough, atomic force microscope, and monolayer particle interaction apparatus. Films without large (μm-sized) holes were prepared by reacting BIEE with the PDMA–PS particles in the ethanol spreading solution for times ≤6 h and then by spreading this solution on a pH 5.8 water surface. Longer reaction times or a pH 9.0 water surface gave films with large holes. The holes were the result of the presence of aggregates of various sizes, which could not efficiently pack in the film. The aggregates were formed by interparticle adhesions because of the BIEE presence and physical attractive forces. The pH 5.8 water gave less aggregation than the pH 9.0 water because of the stronger interparticle electrostatic repulsions that resultedfrom the higher particle charge in pH 5.8 water than pH 9.0 water.The holes in the films could be decreased by reacting BIEE with thePDMA–PS particles on the pH 5.8 or 9.0 water surface, whilethe film was compressed to give a close packing density. The stiffnessof the film of PDMA–PS particles increased, when BIEE was reactedwith the PDMA–PS particles in the spreading solution for 1h and was then spread on a pH 5.8 water surface. The film stiffness,however, did not increase, when BIEE was reacted with PDMA–PSparticles on the pH 5.8 or 9.0 water surface for 1 h. This stiffnessdifference was explained by the fact that the former method gave athicker film than the latter method.
机译:我们研究了如何通过使用交叉电极来改变在空气/水界面处具有聚(2-(N,N-二甲基氨基)甲基丙烯酸甲酯)毛发(PDMA-PS颗粒)的pH响应聚苯乙烯纳米颗粒薄膜的刚度和物理性能。 1,2-双-(2-碘乙氧基)乙烷(BIEE)的连接基并通过改变水的pH值。通过使用Langmuir槽,原子力显微镜和单层颗粒相互作用装置研究了薄膜的物理性能。通过将BIEE与PDMA-PS颗粒在乙醇铺展溶液中反应≤6h,然后将该溶液铺展在pH 5.8的水表面上来制备没有大孔(μm尺寸)的薄膜。较长的反应时间或pH值为9.0的水表面会产生带有大孔的薄膜。这些孔是存在各种尺寸的聚集体的结果,这些聚集体不能有效地包装在薄膜中。由于BIEE的存在和物理吸引力,颗粒之间的粘附形成了聚集体。 pH 5.8的水比pH 9.0的水产生更少的聚集,因为产生了更强的粒子间静电排斥pH 5.8水中的粒子电荷高于pH 9.0水中的粒子电荷。通过使BIEE与pH 5.8或9.0的水表面上的PDMA–PS颗粒,而将膜压缩以得到紧密的堆积密度。刚度BIEE反应后,PDMA–PS颗粒的膜层数增加与PDMA–PS颗粒在撒布溶液中混合1h,然后涂在pH 5.8的水表面。漆膜刚度,但是,当BIEE与PDMA–PS反应时,并没有增加pH 5.8或9.0的水表面上的颗粒持续1小时。这种刚度差异是因为前一种方法给出了比后一种方法更厚的膜。

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