On the nanostructure of polymer layers formed by adsorption from binary and ternary solutions on a solid SiO2 : a combined adsorption and atomic force microscopy (AFM) study
The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO^sub 2^ surface has been estimated from adsorption isotherms and atomic force microscopy (AFM) measurements for polystyrene, poly(butyl methacrylate), and their mixtures. The thickness of the adsorpt...
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Published in: | Colloid and polymer science Vol. 284; no. 8; pp. 893 - 899 |
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01-05-2006
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Abstract | The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO^sub 2^ surface has been estimated from adsorption isotherms and atomic force microscopy (AFM) measurements for polystyrene, poly(butyl methacrylate), and their mixtures. The thickness of the adsorption layers depends strongly on the adsorption conditions and is controlled by several features of the adsorbing entities. In a low-concentration regime of adsorption, the length of polymer chains and the nature of their interaction with the substrate are the most important factors controlling the adsorption process. Above the critical concentration C*, macromolecular clusters (aggregates of several overlapping chains) are formed in a solution as a result of polymer chains self-assembly. Therefore, the final adsorption layer thickness is determined mainly by the size of the clusters in this concentrated regime of adsorption. We also demonstrate that in the case of polymer mixtures, the adsorption leads to formation of mosaic structures with alternation of the polymeric components in plane of the substrate and a characteristic domain size of approximately 200 nm for each of the components. AFM study reveals that the adsorbed layers are fractal structures whose fractal dimensions depend on the type of the polymer and the adsorption process. We demonstrate therefore that the structure of nanolayers of polymers and their mixtures on the solid surface can be regulated by variation of the adsorption conditions.[PUBLICATION ABSTRACT] |
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AbstractList | The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO2 surface has been estimated from adsorption isotherms and atomic force microscopy (AFM) measurements for polystyrene, poly(butyl methacrylate), and their mixtures. The thickness of the adsorption layers depends strongly on the adsorption conditions and is controlled by several features of the adsorbing entities. In a low-concentration regime of adsorption, the length of polymer chains and the nature of their interaction with the substrate are the most important factors controlling the adsorption process. Above the critical concentration C*, macromolecular clusters (aggregates of several overlapping chains) are formed in a solution as a result of polymer chains self-assembly. Therefore, the final adsorption layer thickness is determined mainly by the size of the clusters in this concentrated regime of adsorption. We also demonstrate that in the case of polymer mixtures, the adsorption leads to formation of mosaic structures with alternation of the polymeric components in plane of the substrate and a characteristic domain size of approximately 200 nm for each of the components. AFM study reveals that the adsorbed layers are fractal structures whose fractal dimensions depend on the type of the polymer and the adsorption process. We demonstrate therefore that the structure of nanolayers of polymers and their mixtures on the solid surface can be regulated by variation of the adsorption conditions. The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO^sub 2^ surface has been estimated from adsorption isotherms and atomic force microscopy (AFM) measurements for polystyrene, poly(butyl methacrylate), and their mixtures. The thickness of the adsorption layers depends strongly on the adsorption conditions and is controlled by several features of the adsorbing entities. In a low-concentration regime of adsorption, the length of polymer chains and the nature of their interaction with the substrate are the most important factors controlling the adsorption process. Above the critical concentration C*, macromolecular clusters (aggregates of several overlapping chains) are formed in a solution as a result of polymer chains self-assembly. Therefore, the final adsorption layer thickness is determined mainly by the size of the clusters in this concentrated regime of adsorption. We also demonstrate that in the case of polymer mixtures, the adsorption leads to formation of mosaic structures with alternation of the polymeric components in plane of the substrate and a characteristic domain size of approximately 200 nm for each of the components. AFM study reveals that the adsorbed layers are fractal structures whose fractal dimensions depend on the type of the polymer and the adsorption process. We demonstrate therefore that the structure of nanolayers of polymers and their mixtures on the solid surface can be regulated by variation of the adsorption conditions.[PUBLICATION ABSTRACT] |
Author | KONOVALYUK, V. D CHORNAYA, V. N BLIZNYUK, V. N KATUMENU, R. K TODOSIYCHUK, T. T LIPATOV, Y. S |
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Keywords | Semidilute solution Liquid solid adsorption Coadsorption Nanolayers Surface topography Experimental study Layer thickness Silica Organic solution Polymer mixtures Fractal structures Adsorbed layers Fractal dimension Polymer adsorption from solutions Dilute solution Butyl methacrylate polymer Styrene polymer Self-assembling |
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References | GV Kozlov (1460_CR8) 2003 BJ Fontana (1460_CR19) 1961; 65 A Ulman (1460_CR6) 1991 DH Gracias (1460_CR5) 2002; 14 Y Tretiakov (1460_CR1) 2003; 72 YS Lipatov (1460_CR18) 1975; 37 V Chornaya (1460_CR16) 2002; 255 AN Semenov (1460_CR7) 1996; 29 L Isaacs (1460_CR2) 1999 MM Lerner (1460_CR11) 1997 MN Jones (1460_CR4) 1995 GV Kozlov (1460_CR9) 2001 VN Bliznyuk (1460_CR21) 2001; 167 A Gordon (1460_CR17) 1972 YS Lipatov (1460_CR12) 1988 YS Lipatov (1460_CR13) 1999 M Kawaguchi (1460_CR14) 1992; 37 G Goldbeck-Wood (1460_CR20) 2002; 35 GV Kozlov (1460_CR10) 2002; 9 C Rosa De (1460_CR3) 2000; 405 P Meakin (1460_CR22) 1998 YS Lipatov (1460_CR15) 2002 |
References_xml | – start-page: 1 volume-title: Fractals and local orders in polymer materials year: 2001 ident: 1460_CR9 contributor: fullname: GV Kozlov – volume-title: Handbook of nanophase materials year: 1997 ident: 1460_CR11 contributor: fullname: MM Lerner – volume-title: Fractals, scaling and growth far from equilibrium year: 1998 ident: 1460_CR22 contributor: fullname: P Meakin – volume: 405 start-page: 433 year: 2000 ident: 1460_CR3 publication-title: Nature (Lond) doi: 10.1038/35013018 contributor: fullname: C Rosa De – volume-title: The chemist’s companion year: 1972 ident: 1460_CR17 contributor: fullname: A Gordon – volume-title: Encyclopedia of surface and colloid science year: 2002 ident: 1460_CR15 contributor: fullname: YS Lipatov – volume-title: An introduction to ultrathin organic films. From Langmuir–Blodgett to self-assembly year: 1991 ident: 1460_CR6 contributor: fullname: A Ulman – volume: 37 start-page: 219 year: 1992 ident: 1460_CR14 publication-title: Adv Colloid Interface Sci doi: 10.1016/0001-8686(92)80085-C contributor: fullname: M Kawaguchi – volume: 35 start-page: 5283 year: 2002 ident: 1460_CR20 publication-title: Macromolecules doi: 10.1021/ma0119777 contributor: fullname: G Goldbeck-Wood – volume: 72 start-page: 721 year: 2003 ident: 1460_CR1 publication-title: Russian Progr Chem contributor: fullname: Y Tretiakov – volume: 65 start-page: 480 issue: 3 year: 1961 ident: 1460_CR19 publication-title: J Phys Chem doi: 10.1021/j100821a023 contributor: fullname: BJ Fontana – volume: 9 start-page: 509 year: 2002 ident: 1460_CR10 publication-title: Compos Interfaces doi: 10.1163/15685540260494092 contributor: fullname: GV Kozlov – volume-title: Polymer interfaces and emulsions year: 1999 ident: 1460_CR13 contributor: fullname: YS Lipatov – volume: 255 start-page: 36 year: 2002 ident: 1460_CR16 publication-title: J Colloid Interface Sci doi: 10.1006/jcis.2002.8609 contributor: fullname: V Chornaya – volume: 167 start-page: 89 year: 2001 ident: 1460_CR21 publication-title: Macromol Symp doi: 10.1002/1521-3900(200103)167:1<89::AID-MASY89>3.0.CO;2-S contributor: fullname: VN Bliznyuk – volume-title: Colloid chemistry of polymers year: 1988 ident: 1460_CR12 contributor: fullname: YS Lipatov – volume-title: Micelles, monolayers and biomembranes year: 1995 ident: 1460_CR4 contributor: fullname: MN Jones – volume: 29 start-page: 2179 year: 1996 ident: 1460_CR7 publication-title: Macromolecules doi: 10.1021/ma950712n contributor: fullname: AN Semenov – volume: 14 start-page: 235 year: 2002 ident: 1460_CR5 publication-title: Adv Mater doi: 10.1002/1521-4095(20020205)14:3<235::AID-ADMA235>3.0.CO;2-B contributor: fullname: DH Gracias – volume-title: Supramolecular technology year: 1999 ident: 1460_CR2 contributor: fullname: L Isaacs – volume-title: Fractal analysis of polymers year: 2003 ident: 1460_CR8 contributor: fullname: GV Kozlov – volume: 37 start-page: 247 year: 1975 ident: 1460_CR18 publication-title: Colloid J USSR contributor: fullname: YS Lipatov |
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Snippet | The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO^sub 2^ surface has been estimated from adsorption... The thickness of nanolayers formed by adsorption from dilute and semi-dilute solutions on a solid SiO2 surface has been estimated from adsorption isotherms and... |
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SubjectTerms | Adsorption Applied sciences Atomic force microscopy Chains (polymeric) Exact sciences and technology Fractal analysis Fractals Microscopy Nanomaterials Nanostructure Organic polymers Physicochemistry of polymers Polymers Properties and characterization Self assembly Solution and gel properties Surface chemistry |
Title | On the nanostructure of polymer layers formed by adsorption from binary and ternary solutions on a solid SiO2 : a combined adsorption and atomic force microscopy (AFM) study |
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