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Volumn 31, Issue 13, 1998, Pages 4272-4276

Synthesis and surface energy measurement of semi-fluorinated, low-energy surfaces

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; ELASTOMERS; FLUORINE; HYDROLYSIS; HYSTERESIS; INTERFACIAL ENERGY;

EID: 0032096279     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma9700993     Document Type: Article
Times cited : (39)

References (20)
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    • Viney, C.; Russell, T. P.; Depero, L. E.; Twieg, R. J. Mol. Cryst. Liq. Cryst. 1989, 168, 63. Viney, C.; Twieg, R. J.; Russell, T. P.; Depero, L. E. Liq. Cryst. 1989, 5, 1783. Russell, T. P.; Rabolt, J. F.; Twieg, R. J.; Siemens, R. L. Macromolecules 1986, 19, 1135.
    • (1989) Liq. Cryst. , vol.5 , pp. 1783
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    • Viney, C.; Russell, T. P.; Depero, L. E.; Twieg, R. J. Mol. Cryst. Liq. Cryst. 1989, 168, 63. Viney, C.; Twieg, R. J.; Russell, T. P.; Depero, L. E. Liq. Cryst. 1989, 5, 1783. Russell, T. P.; Rabolt, J. F.; Twieg, R. J.; Siemens, R. L. Macromolecules 1986, 19, 1135.
    • (1986) Macromolecules , vol.19 , pp. 1135
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    • (1992) Makromol. Chem. , vol.193 , pp. 275-284
    • Hopken, J.1    Moller, M.2    Lee, M.S.3    Percec, V.4
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    • Hopken, J.; Moller, M.; Lee, M. S.; Percec, V. Makromol. Chem. 1992, 193, 275-284. Percee, V.; Schlueter, D.; Ungar, G. Macromolecules 1997, 30, 645-648. Beyou, E.; Bennetau, B.; Dunoguès, J.; Babin, P.; Teyssié, D.; Boileau, S.; Corpart, J.-M. Polym. Int. 1995, 38, 237-244.
    • (1997) Macromolecules , vol.30 , pp. 645-648
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    • Davidson, T.; Griffin, A. C.; Wilson, L. M.; Windle, A. H. Macromolecules 1995, 28, 354-357. Hoyle, C. E.; Kang, D.; Jariwala, C.; Griffin, A. C. Polymer 1993, 34, 3070-3075.
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    • note
    • Error for all XPS composition measurements was ±0.1%. The remaining composition of the samples (without H) with 4.8% F was 47.2% C, 23.0% Si, and 25.0% O. No Cl was observable. On the basis of the 4.8% F and the stoichiometry of the attached SFG group and the unmodified PDMS, the theoretical composition should be 4.8% F, 49.5% C, 22.5% Si, and 23.5% O. The increased O and decreased C observed relative to the computed composition probably results from silanol end groups created by the HCl treatment that have not reacted with the SFG groups.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.