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Surface morphology of latex film formed from poly(butyl methacrylate) latex in the presence of alkali-soluble resin

机译:在碱溶性树脂存在下由聚甲基丙烯酸丁酯胶乳形成的胶乳膜的表面形态

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The film morphology of emulsifier-free poly(n-butyl methacrylate) (PBMA) latex in the presence of post-added alkali-soluble resin (ASR) was studied using atomic force microscopy (AFM). The film morphology was monitored, from the nascent stage after water was evaporated from the dispersion, as a function of annealing temperature and its duration. The AFM results suggest strongly the formation of a hard shell of ASR, namely poly(styrene/alpha-methylstyrene/acrylic acid) (SAA) over the soft PBMA particle. During annealing, the incompatibility of the two polymers leads to the migration and accumulation of SAA at the interstices and interfacial regions among the arrays of PBMA particles, and also at the film surface. The hard shell of SAA retards the diffusion of the PBMA molecules across the particle/particle interface and slows down the gradual coalescence of film formation. Annealing at high temperature ruptures the SAA shells and the PBMA particles interdiffuse at a faster rate than the SAA due to its lower Tg compared to that of SAA. The difference in the rates of fusion of the SAA and PBMA phases leads to the formation of indentations on individual particles at high annealing temperature and long annealing duration. The occurrence of this feature increases with the annealing temperature and its duration. These indentations are eventually transformed into `depressions' on the latex films when the indentations at the top of the individual particles sag inwords at sufficiently high annealing temperature and long annealing time. The surface enrichment of SAA is confirmed by the results of fainer transform infrared spectroscopy with attenuated internal reflectance of the film surface.
机译:使用原子力显微镜(AFM)研究了无乳化剂的聚甲基丙烯酸正丁酯(PBMA)在后添加碱溶性树脂(ASR)存在下的薄膜形态。在水从分散体中蒸发之后的新生阶段,根据退火温度及其持续时间来监测膜的形态。 AFM结果强烈表明ASR的硬壳,即在柔软的PBMA颗粒上形成了聚(苯乙烯/α-甲基苯乙烯/丙烯酸)(SAA)。在退火期间,两种聚合物的不相容性导致SAA在PBMA颗粒阵列之间的间隙和界面区域以及薄膜表面迁移和积累。 SAA的硬壳阻碍了PBMA分子在颗粒/颗粒界面上的扩散,并减慢了膜形成的逐渐结合。高温退火使SAA壳破裂,并且PBMA颗粒的Tg比SAA低,因此其扩散速度比SAA快。 SAA和PBMA相的熔融速率不同会导致在较高的退火温度和较长的退火时间下在单个颗粒上形成压痕。该特征的发生随着退火温度及其持续时间的增加而增加。当在足够高的退火温度和较长的退火时间下,单个颗粒顶部的凹痕下垂时,这些凹痕最终会在乳胶薄膜上转变为“凹痕”。 SAA的表面富集是通过Fainer变换红外光谱法得到的,该结果具有薄膜表面的内部反射率降低的特征。

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