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通过紫外线诱导交联快速制备刷状涂层

Rapid Processing of Bottlebrush Coatings through UV-Induced Cross-Linking.

作者信息

Mei Hao, Mah Adeline Huizhen, Hu Zhiqi, Li Yilin, Terlier Tanguy, Stein Gila E, Verduzco Rafael

机构信息

Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas 77005, United States.

Nanosystems Engineering Research Center for Nanotechnology-Enabled Water Treatment, Rice University, Houston, Texas 77005, United States.

出版信息

ACS Macro Lett. 2020 Aug 18;9(8):1135-1142. doi: 10.1021/acsmacrolett.0c00384. Epub 2020 Jul 22.

Abstract

Bottlebrush polymers can be used to introduce novel surface properties including hydrophilicity, stimuli-responsiveness, and reduced friction forces. However, simple, general, and efficient approaches to cross-linking bottlebrush polymer films and coatings are limited. Here, we report that bottlebrush polymers with an unsaturated polynorbornene backbone and thiol-terminated side chains can be cross-linked on demand by UV irradiation to produce uniform and insoluble bottlebrush polymer coatings. To quantify the kinetics and efficiency of cross-linking by UV exposure (254 nm), we measured the normalized residual thickness (NRT) of bottlebrush and linear polymer films after UV exposure and solvent washing. For bottlebrush polymers with thiol-terminated polystyrene (PS) side chains, the NRT exceeded 60% for a UV dose of 1.0 J/cm, while unfunctionalized linear PS required a dose of 7.9 J/cm to achieve similar NRT values. Rapid UV-induced cross-linking of the bottlebrush PS was attributed to the thiol-ene coupling of the thiol-terminated side chains with the unsaturated polynorbornene backbones, as demonstrated through FTIR measurements and control studies involving bottlebrush polymers with saturated backbones. To establish the broader applicability of this approach, UV-induced cross-linking was demonstrated for thin films of bottlebrush polymers with thiol-terminated poly(methyl acrylate) (BB-PMMA-SH) side chains and those with poly(ethylene glycol) (BB-PEG) and poly(lactic acid) (BB-PLA) side chains which do not contain thiol end groups. UV-induced cross-linking of BB-PEG and BB-PLA films required the use of a multifunctional thiol additive. Finally, we demonstrated that bottlebrush polymer multilayers can be fabricated through sequential deposition and UV-induced cross-linking of different bottlebrush polymer chemistries. The cross-linking process outlined in this work is simple, general, and efficient and produces solvent-resistant coatings that preserve the unique properties and functions of bottlebrush polymers.

摘要

刷状聚合物可用于引入包括亲水性、刺激响应性和降低摩擦力在内的新型表面特性。然而,用于交联刷状聚合物薄膜和涂层的简单、通用且有效的方法有限。在此,我们报道了具有不饱和聚降冰片烯主链和硫醇封端侧链的刷状聚合物可通过紫外线照射按需交联,以制备均匀且不溶性的刷状聚合物涂层。为了量化紫外线照射(254 nm)交联的动力学和效率,我们测量了紫外线照射和溶剂洗涤后刷状聚合物和线性聚合物薄膜的归一化残余厚度(NRT)。对于具有硫醇封端聚苯乙烯(PS)侧链的刷状聚合物,紫外线剂量为1.0 J/cm²时,NRT超过60%,而未官能化的线性PS需要7.9 J/cm²的剂量才能达到类似的NRT值。刷状PS的快速紫外线诱导交联归因于硫醇封端侧链与不饱和聚降冰片烯主链的硫醇-烯偶联,这通过傅里叶变换红外光谱(FTIR)测量以及涉及具有饱和主链的刷状聚合物的对照研究得到证明。为了确立该方法更广泛的适用性,对具有硫醇封端聚(甲基丙烯酸甲酯)(BB-PMMA-SH)侧链以及具有聚(乙二醇)(BB-PEG)和聚(乳酸)(BB-PLA)侧链(不含硫醇端基)的刷状聚合物薄膜进行了紫外线诱导交联演示。BB-PEG和BB-PLA薄膜的紫外线诱导交联需要使用多功能硫醇添加剂。最后,我们证明了刷状聚合物多层膜可通过不同刷状聚合物化学组成的顺序沉积和紫外线诱导交联来制备。这项工作中概述的交联过程简单、通用且有效,并产生了保留刷状聚合物独特性能和功能的耐溶剂涂层。

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