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溶胶-凝胶法制备的 TiO 薄膜在不同类型塑料基底上的转移和附着。

Transferability and Adhesion of Sol-Gel-Derived Crystalline TiO Thin Films to Different Types of Plastic Substrates.

机构信息

Graduate School of Science and Engineering, Kansai University , 3-3-35 Yamate-cho, Suita 564-8680, Japan.

Faculty of Chemistry, Materials and Bioengineering, Kansai University , 3-3-35 Yamate-cho, Suita 564-8680, Japan.

出版信息

Langmuir. 2017 Jan 31;33(4):947-953. doi: 10.1021/acs.langmuir.6b04142. Epub 2017 Jan 20.

Abstract

Anatase thin films were prepared on various plastic substrates by our recently developed sol-gel transfer technique. Polycarbonate (PC), poly(methyl methacrylate) (PMMA), polyethylene terephthalate (PET), polyethylene (PE), polypropylene (PP), polyether ether ketone (PEEK), and polyvinylidene chloride (PVDC) were employed as plastic substrates. A Si(100) substrate was first coated with a polyimide (PI)/polyvinylpyrrolidone (PVP) mixture layer, and an alkoxide-derived titania gel film was deposited on it by spin-coating. The resulting titania gel film was heated to 600 °C, during which the PI/PVP layer decomposed and the gel film was converted into a 60 nm thick anatase film. The anatase film was then transferred from the Si(100) substrate to the plastic substrate. This was achieved by heating the plastic/anatase/Si(100) stack in a near-infrared image furnace to 120-350 °C, depending on the type of plastic substrate, under unidirectional pressure. The anatase film cracked during transfer to PE, PP, PEEK, and PVDC substrates but did not crack during transfer to PC, PMMA, and PET substrates. The fraction of the total film area that was successfully transferred was assessed with the aid of image analysis. This fraction tended to be large for plastics with C═O and C-O groups and small for those without these groups. The film/substrate adhesion assessed by cross-cut tape tests also tended to be high for plastics with C═O and C-O groups and low for those without these groups. The adhesion to plastics without C═O or C-O groups could be enhanced and their transfer area fraction increased by oxidizing the native plastic surface by ultraviolet-ozone treatment prior to transfer.

摘要

锐钛矿薄膜通过我们最近开发的溶胶-凝胶转移技术在各种塑料基底上制备。聚碳酸酯(PC)、聚甲基丙烯酸甲酯(PMMA)、聚对苯二甲酸乙二醇酯(PET)、聚乙烯(PE)、聚丙烯(PP)、聚醚醚酮(PEEK)和聚偏二氯乙烯(PVDC)被用作塑料基底。首先,在 Si(100) 衬底上涂覆一层聚酰亚胺(PI)/聚乙烯吡咯烷酮(PVP)混合物层,然后通过旋涂在其上沉积醇盐衍生的二氧化钛凝胶膜。所得的二氧化钛凝胶膜被加热至 600°C,在此期间,PI/PVP 层分解,凝胶膜转化为 60nm 厚的锐钛矿膜。然后将锐钛矿膜从 Si(100) 衬底转移到塑料衬底上。这是通过在近红外图像炉中加热塑料/锐钛矿/Si(100) 叠层来实现的,取决于塑料基底的类型,在单向压力下,加热温度为 120-350°C。在将锐钛矿膜转移到 PE、PP、PEEK 和 PVDC 基底时,膜会发生开裂,但在转移到 PC、PMMA 和 PET 基底时,膜不会开裂。借助图像分析评估了总膜面积中成功转移的部分。对于具有 C═O 和 C-O 基团的塑料,该部分趋于较大,对于没有这些基团的塑料,该部分趋于较小。通过在转移之前用紫外线-臭氧处理对天然塑料表面进行氧化,可以增强与没有 C═O 或 C-O 基团的塑料的附着力,并增加其转移面积分数。

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