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Thermally responsive wettability of self-assembled methvlcellulose nanolavers

机译:自组装甲基纤维素纳米层的热响应润湿性

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Thermo-responsive cellulosic nanolayers were prepared from methylcellulose (MC), which is known to have a unique lower critical solution temperature. Thiosemicarbazide (TSC) was selectively introduced into the MC reducing end groups, and the corresponding MC-TSC derivative was spontaneously chemisorbed on an Au substrate at 4 ℃ to give MC self-assembled monolayers (SAMs). Linear MC chains were stably fixed onto the Au substrate, yielding an MC-SAM of thickness ca. 15 nm with a root mean square value less than 1 nm. The MC-SAM surface exhibited thermally responsive wetting characteristics; the water contact angle was found to rise and fall around 70 ℃, possibly due to the solid-state phase transition of the MC nanolayers resulting from the inherent gelation of MC molecules in water. Such wetting behavior was shown to be reversible following repeated heating and cooling. The MC-SAM immersed in salt solution revealed lower phase transition temperatures, and an increase in sodium chloride concentration ranging from 0.0 to 1.0 M brought about a dramatic decrease in the apparent phase transition temperature from ca. 70 to 30 ℃. For the purposely designed MC nanolayers, such controllable wetting properties are expected to prompt growing interest in the applications of cellulosic biopolymer interfaces.
机译:由甲基纤维素(MC)制备热响应性纤维素纳米层,已知该甲基纤维素具有独特的较低的临界溶液温度。将硫代氨基脲(TSC)选择性地引入MC还原端基中,并将相应的MC-TSC衍生物在4℃下自发化学吸附在Au基底上,得到MC自组装单层膜(SAMs)。线性MC链稳定地固定在Au基底上,从而产生厚度约为ca的MC-SAM。 15纳米,均方根值小于1纳米。 MC-SAM表面表现出热响应润湿特性。发现水接触角在70℃左右上升或下降,这可能是由于MC分子在水中固有的胶凝作用导致了MC纳米层的固态相变。在反复加热和冷却后,这种润湿行为被证明是可逆的。浸入盐溶液中的MC-SAM显示出较低的相变温度,而氯化钠浓度从0.0到1.0 M升高,导致表观相变温度从约℃急剧降低。 70至30℃。对于有目的地设计的MC纳米层,这种可控的润湿性能有望促进人们对纤维素生物聚合物界面应用的兴趣。

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