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The ultra-durable, self-healing superhydrophobic polyester fabric based on ZnO@PDMS nanoparticle composite coating (PET-g-PDMS@ZnO fiber) is prepared by low-temperature plasma polymerization. The influences of the preparation process on the superhydrophobicity, self-healing property, durability and stability of the coating are studied. The results show that the water contact angle on the surface of PET-g-PDMS@ZnO fabric can reach 162.7°, and the sliding angle is 7.5°. After 300 washing cycles and 1300 rubbing cycles, the superhydrophobic property is still maintained. Both plasma method and heating method are used to repair the worn coating, and it is found that the repair effect of plasma is obvious, while the heating repair is effective only in the case of small loads. Moreover, scanning electron microscope, nanoindentation and X-ray photoelectron spectroscopy measurement are used to explore the self-healing mechanism. This research provides the theoretical and technical support for the development and application of plasma technology in the preparation of superhydrophobic fabrics.
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Keywords:
- plasma /
- polyester /
- superhydrophobic /
- durability /
- self-healing
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Google Scholar
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[3] 王奔, 念敬妍, 铁璐, 张来斌, 郭志光 2013 物理学报 62 146801
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Google Scholar
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Google Scholar
[14] Su X J, Li H Q, Lai X J, Zhang L, Wang J, Liao X F, Zeng X R 2017 ACS Appl. Mater. Interfaces 9 28089
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[15] Li Y, Li L, Sun J Q 2010 Angew. Chem.Int. Ed. 49 6129
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Google Scholar
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图 1 (a) 超疏水织物的制备流程; (b) 不同液滴在超疏水织物表面的铺展图; 不同纤维表面的SEM图像, 其中图(c)—(e)分别对应(c) 涤纶纤维原样, (d) PET-g-PDMS, (e) PET-g-PDMS@ZnO; 不同纤维表面的AFM图像, 其中图(f)—(h)分别对应(f) 涤纶纤维原样, (g) PET-g-PDMS, (h) PET-g-PDMS@ZnO
Figure 1. (a) Preparation process of superhydrophobic fabric. (b) Spreading image of different droplets on the surface of superhydrophobic fabric. SEM images of different fiber surfaces: (c) Untreated; (d) PET-g-PDMS; (e) PET-g-PDMS@ZnO. AFM images of different fiber surfaces: (f) Untreated; (g) PET-g-PDMS; (h) PET-g-PDMS@ZnO.
图 2 (a)气体压强、(b)功率、(c)放电时间和(d)循环次数对PET-g-PDMS@ZnO织物水接触角的影响; 不同放电时间处理的纤维表面的SEM图像, 其中图(e), (f)对应的放电时间分别为(e) 15 s; (f) 100 s
Figure 2. Effects of (a) gas pressure, (b) power, (c) discharge time, and (d) washing times on the WCA of PET-g-PDMS@ZnO fabric; SEM images of fiber surface treated with different discharge time: (e) 15 s; (f) 100 s.
图 3 (a) 水接触角和滚动角与摩擦循环之间的关系; (b) 自修复流程图; 水接触角与(c)等离子体和(d)加热自修复循环次数之间的关系
Figure 3. (a) Relationship of WCA and sliding angle to friction cycle; (b) self-healing flow chart; relationship of WCA to the number of (c) plasma and (d) heating self-healing cycles.
图 4 PET-g-PDMS@ZnO纤维自修复前后SEM图像, 其中图(a)—(d)分别对应(a) PET-g-PDMS@ZnO纤维原样, (b) 磨擦400次后, (c) 等离子体处理修复后, (d) 加热(80 ℃, 30 min)修复后; (e) PDMS膜的纳米压痕
Figure 4. SEM images of PET-g-PDMS@ZnO fiber before and after self-healing: (a) PET-g-PDMS@ZnO fiber; (b) 400 rubs; (c) plasma treatment; (d) heating (80 ℃, 30 min). (e) Nanoindentation of PDMS film on the surface of PET-g-PDMS fiber.
图 5 自修复前后织物表面C 1s元素的XPS图像 (a) 原样; (b) PET-g-PDMS@ZnO织物; (c) 摩擦400次; (d) 等离子体法修复; (e) 加热法修复
Figure 5. XPS images of C 1s elements on the fabric surface before and after self-healing: (a) Fabric; (b) PET-g-PDMS@ZnO fabric; (c) rubbing 400 times; (d) plasma repairing; (e) heating repair.
表 1 不同样品表面元素含量
Table 1. Surface element content of different samples.
结合能/eV 化学键 原样 PET-g-PDMS@ZnO织物 摩擦400次 等离子体法修复 加热法修复 289.3 O—C=O 8.94 — 5.67 — 3.23 286.8 C=O 18.56 6.75 10.29 7.51 9.54 284.8 C—C 72.51 93.25 84.04 92.49 89.23 
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[1] Dimitrakellis P, Gogolides E 2018 Adv. Colloid Interface Sci. 254 1
Google Scholar
[2] Tsougeni K, Vourdas N, Tserepi A, Gogolides E, Cardinaud C 2009 Langmuir 25 11748
Google Scholar
[3] 王奔, 念敬妍, 铁璐, 张来斌, 郭志光 2013 物理学报 62 146801
Google Scholar
Wang B, Nian J Y, Tie L, Zhang Y B, Guo Z G 2013 Acta Phys. Sin. 62 146801
Google Scholar
[4] Liu H, Huang J Y, Chen Z, Chen G Q, Zhang K Q, Al-Deyab S S, Lai Y K 2017 Chem. Eng. J. 330 26
Google Scholar
[5] Zimmermann J, Reifler F A, Fortunato G, Gerhardt L C, Seeger S 2008 Adv. Funct. Mater. 18 3662
Google Scholar
[6] Deng B, Cai R, Yu Y, Jiang H Q, Wang C L, Li J A, Li L F, Yu M, Li J Y, Xie L D, Huang Q, Fan C H 2010 Adv. Mater. 22 5473
Google Scholar
[7] Xue C H, Li X, Jia S T, Guo X J, Li M 2016 RSC Adv. 6 84887
Google Scholar
[8] Liu S, Zhou H, Wang H X, Yang W D, Shao H, Fu S D, Zhao Y, Liu D Q, Feng Z H, Lin T 2017 Small 13 1701891
Google Scholar
[9] Kong L Z, Tu K K, Guan H, Wang X Q 2017 Appl. Surf. Sci. 407 479
Google Scholar
[10] Fu S D, Zhou H, Wang H X, Ding J, Liu S, Zhao Y, Niu H T, Rutledge G C, Lin T 2018 RSC Adv. 8 717
Google Scholar
[11] Abbas R, Khereby M A, Sadik W A, El Demerdash A G M 2015 Cellulose 22 887
Google Scholar
[12] Zhao Q, Wu L, Huang H, Liu Y C 2016 Mater. Des. 92 541
Google Scholar
[13] Oh J H, Ko T J, Moon M W, Park C H 2017 RSC Adv. 7 25597
Google Scholar
[14] Su X J, Li H Q, Lai X J, Zhang L, Wang J, Liao X F, Zeng X R 2017 ACS Appl. Mater. Interfaces 9 28089
Google Scholar
[15] Li Y, Li L, Sun J Q 2010 Angew. Chem.Int. Ed. 49 6129
Google Scholar
[16] Zhang H, Hou C P, Song L X, Ma Y, Ali Z, Gu J W, Zhang B L, Zhang H P, Zhang Q Y 2018 Chem. Eng. J. 334 598
Google Scholar
[17] Xu L Y, Yang L L, Yang S, Xu Z, Lin G J, Shi J J, Zhang R Y, Yu J Y, Ge D T, Guo Y 2021 ACS Appl. Mater. Interfaces 13 6758
Google Scholar
[18] Lee J, Hwang S, Cho D H, Hong J, Shin J H, Byun D 2017 Appl. Surf. Sci. 394 543
Google Scholar
[19] Jiang C, Liu W Q, Yang M P, Liu C H, He S, Xie Y K, Wang Z F 2019 Appl. Surf. Sci. 463 34
Google Scholar
[20] Zhao N, Xie Q D, Weng L H, Wang S Q, Zhang X Y, Xu J 2005 Macromolecules 38 8996
Google Scholar
[21] Qian Z Y, Risan J, Stadnick B, McKenna G B 2018 J. Polym. Sci., Part B: Polym. Phys. 56 414
Google Scholar
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