Formation of hydrophobic self-assembled monolayers on paper surface with silanes
- Authors
- Jeong, O.M.; Hyoung, L.; Paik, K.-H.
- Issue Date
- 2010
- Keywords
- Silanes; Monolayers
- Citation
- Palpu Chongi Gisul/Journal of Korea Technical Association of the Pulp and Paper Industry, v.42, no.1, pp.64 - 73
- Indexed
- SCOPUS
KCI
- Journal Title
- Palpu Chongi Gisul/Journal of Korea Technical Association of the Pulp and Paper Industry
- Volume
- 42
- Number
- 1
- Start Page
- 64
- End Page
- 73
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/118261
- ISSN
- 0253-3200
- Abstract
- This study was conducted to modify the surface properties of papers by formation of hydrophobic self-assembled monolayers AM) on paper surface with silanes. A base paper I(0.5% AKD) and base paper II(1.0-1.5% AKD) were reacted with silanes(PFDTES, DMDCS, MODDCS) by immersion method and vapor deposition method. Hydrophobic SAMs(contact angle value> 120) were obtained on all papers after treatment with 10 μl PFDTES for 15min, with 50μl DMDCS for 30min, with 50μl MODDCS for 300min. When applying PFDTES to paper surface, lower silane concentration and shorter reaction time were required, whereas MODDCS with long alkyl chain required the longest reaction time of 300min. The stöckight sizing degree of silane treated papers were increased between 105sec(base paper I) and 130sec(base paper II). The wet tensile strength of PFDTES-treated base papers(I, II) increased by 10-34% after SAM formation. However, the wet tensile strength of the DMDCS-treated base paper(I) was found to decrease from 0.067kN/m to 0.038kN/m; this may due to the cellulose degrading as a result of generated hydrogen chloride when hydroxyl group of cellulose were reacted with DMDCS. No apparent changes of PPS roughness on silane-treated papers are observed. The ATR-IR spectrum showed absorption peak located at 465 and 1200cm-1 which can be assigned to the Si-O-C asymmetric stretching and Si-O-C bonds, respectively.
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Collections - College of Life Sciences and Biotechnology > Division of Environmental Science and Ecological Engineering > 1. Journal Articles
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