Changes in the wettability of the surface of soda-lime glass and of sol-gel-derived lithium silicate thin films during storage at room temperature

被引:0
|
作者
Kozuka, Hiromitsu [1 ]
Miyao, Yuta [1 ]
Kato, Tomoaki [1 ]
Miki, Manato [1 ]
机构
[1] Kansai Univ, Dept Chem & Mat Engn, 3-3-35 Yamate Cho, Suita 5648680, Japan
关键词
Wettability; Contact angle; Soda-lime glass; Lithium silicate thin film; Ion-excahnge; CHEMICAL-PROPERTIES; OH GROUPS; OXIDE; WATER; SUPERHYDROPHILICITY; ADSORPTION; DEGRADATION; CHEMISTRY; DYNAMICS; TENSION;
D O I
10.1007/s10971-024-06523-5
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Maintaining the water wettability for extended period is generally tough to achieve on solid surface. We stored a soda-lime glass plate in a container equipped with an air purifier with a fan filter, where the water contact angle increased from 3 degrees to 33 degrees in 2 days. X-ray photoelectron spectroscopic (XPS) spectra obtained on the glass surface showed that hydrocarbons increased in amount during storage, indicating their adsorption as one of the causes of the increased contact angle during storing. Next we prepared lithium silicate thin films with nominal Li/Si mole ratios of 0.12-0.86 on Si(100) wafers by sol-gel method from lithium nitrate-tetraethyl orthosilicate solutions. The films were stored in the container with the air purifier, and the water contact angle was measured as a function of storage time. The films of Li/Si >= 0.24 kept contact angles lower than 15 degrees over 10 days although hydrocarbons increased in amount on the surface during storage, which was examined by XPS analysis on the film of Li/Si = 0.24. The film surface turned cloudy during storage, which we attributed to lithium carbonate precipitates by field emission scanning electron microscopy (FE-SEM) and infrared (IR) absorption spectroscopy. We thought that hydrocarbons adsorbed on lithium carbonate precipitates may be washed out when a water droplet is placed on the film surface in contact angle measurements, and that such hydrocarbon removal may lead to the long-term duration of the low contact angle. Elemental depth profile analysis by XPS showed that Li+ ions leach out from the film during soaking in water, resulting in the formation of a silica film. We expected the resulting silica film to be porous and hence to exhibit persistent low water contact angle due to capillary effect. However, the film showed higher initial contact angles, which further increased during storing. The silica film was unexpectedly relatively dense, which was revealed by refractive index measurements, not having porous nature with persistent hydrophilicity.Graphical AbstractWater contact angle on soda-lime glass surface increased during storage in air, while adsorbed hydrocarbon increased in amount. Sol-gel-derived lithium silicate thin films kept low contact angles during storage while adsorbed hydrocarbon increased. Li+ ions leached out when the film was soaked in water. The water contact angle on a soda-lime glass plate surface increased during storage in the air.Hydrocarbons increased in amount on the glass plate surface during storage.Lithium silicate thin films prepared from LiNO3-Si(OC2H5)4 solution kept contact angles lower than 15 degrees for during storage over 300 h.Li+ ions leached out when the lithium silicate film was soaked in water.The soaked film showed significant increase in contact angle during storage.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] Nano-quantum size effect in sol-gel derived mesoporous titania layers deposited on soda-lime glass substrate
    Gondek, Ewa
    Karasinski, Pawel
    Drewniak, Sabina
    PHYSICA E-LOW-DIMENSIONAL SYSTEMS & NANOSTRUCTURES, 2014, 62 : 128 - 135
  • [22] Effect of Annealing Temperature on Structural and Optical Properties of Sol-Gel-Derived ZnO Thin Films
    Arif, Mohd.
    Sanger, Amit
    Vilarinho, Paula M.
    Singh, Arun
    JOURNAL OF ELECTRONIC MATERIALS, 2018, 47 (07) : 3678 - 3684
  • [23] Sol-Gel-Derived Iron Oxide Thin Films on Silicon: Surface Properties and Interfacial Chemistry
    Park, Chi-dong
    Walker, Jeremy
    Tannenbaum, Rina
    Stiegman, A. E.
    Frydrych, J.
    Machala, L.
    ACS APPLIED MATERIALS & INTERFACES, 2009, 1 (09) : 1843 - 1846
  • [24] Low-Temperature Process for Direct Formation of MoS2 Thin Films on Soda-Lime Glass Substrates
    Ma, Sang Min
    Kwon, Sang Jik
    Cho, Eou-Sik
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2019, 19 (03) : 1439 - 1444
  • [25] Gaining insight into the nanoscale properties of sol-gel-derived silicate thin films by single-molecule spectroscopy
    Higgins, DA
    Collinson, MM
    LANGMUIR, 2005, 21 (20) : 9023 - 9031
  • [26] Pressureless joining of soda lime silicate glass using polysilazane-derived silica at near-room temperature
    Karacasulu, Levent
    Biesuz, Mattia
    Pastorelli, Virginia
    Vakifahmetoglu, Cekdar
    Sglavo, Vincenzo M.
    Ferraris, Monica
    Soraru, Gian D.
    CERAMICS INTERNATIONAL, 2025, 51 (05) : 5747 - 5753
  • [27] CHEMICAL DURABILITY OF SODA-LIME-SILICA GLASS BOTTLES COATED WITH SOL-GEL DERIVED SILICA FILMS
    AHMED, AA
    RAMADAN, NA
    YOUSSOF, IM
    GLASS TECHNOLOGY, 1995, 36 (02): : 54 - 60
  • [28] FACTORS AND MECHANISM OF CHANGES IN THE REFRACTIVE-INDEX OF SOL-GEL DERIVED 80TIO2.20SIO2 FILMS COATED ON SODA-LIME-SILICATE GLASS SUBSTRATES
    KIM, BO
    CHUNG, SJ
    NIPPON SERAMIKKUSU KYOKAI GAKUJUTSU RONBUNSHI-JOURNAL OF THE CERAMIC SOCIETY OF JAPAN, 1993, 101 (12): : 1324 - 1329
  • [29] Apparent relaxation of in-plane residual stress of sol-gel-derived crystalline and glass oxide thin films
    Kozuka, Hiromitsu
    Kitano, Sosuke
    Nishimura, Yuki
    Koizumi, Yuta
    JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY, 2020, 95 (03) : 710 - 718
  • [30] Effects of acetic acid on the crystallization temperature of sol-gel-derived MgO nano-powders and thin films
    Kim, JY
    Jung, HS
    Hong, KS
    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2005, 88 (03) : 784 - 787