排序方式: 共有42条查询结果,搜索用时 15 毫秒
1.
Alexopoulos T Allen C Anderson EW Areti H Banerjee S Beery PD Biswas NN Bujak A Carmony DD Carter T Cole P Choi Y De Bonte RJ Erwin AR Findeisen C Goshaw AT Gutay LJ Hirsch AS Hojvat C Kenney VP Lindsey CS LoSecco JM McMahon T McManus AP Morgan N Nelson KS Oh SH Piekarz J Porile NT Reeves D Scharenberg RP Stampke SR Stringfellow BC Thompson MA Turkot F Walker WD Wang CH Wesson DK 《Physical review letters》1990,64(9):991-994
2.
Lazarus EA Navratil GA Greenfield CM Strait EJ Austin ME Burrell KH Casper TA Baker DR DeBoo JC Doyle EJ Durst R Ferron JR Forest CB Gohil P Groebner RJ Heidbrink WW Hong R Houlberg WA Howald AW Hsieh C Hyatt AW Jackson GL Kim J Lao LL Lasnier CJ Leonard AW Lohr J La Haye RJ Maingi R Miller RL Murakami M Osborne TH Perkins LJ Petty CC Rettig CL Rhodes TL Rice BW Sabbagh SA Schissel DP Scoville JT Snider RT Staebler GM Stallard BW Stambaugh RD St John HE Stockdale RE Taylor PL Thomas DM 《Physical review letters》1996,77(13):2714-2717
3.
4.
5.
Costa AC Composto RJ Vlcek P Geoghegan M 《The European physical journal. E, Soft matter》2005,18(2):159-166
Using neutron reflectometry, the adsorption of diblock copolymers from a neutral polystyrene (PS) matrix is studied as a function
of substrate type and non-adsorbing block degree of polymerization. The block copolymer is poly(deutero styrene)-block-poly(methyl methacrylate) and the substrates are silicon oxide, SiOx, and SiOx functionalized with (3-aminopropyl)triethoxysilane (APTES). We have determined the equilibrium volume fraction-depth profiles
for such films, and compared them with volume fraction profiles generated by self-consistent mean-field (SCMF) theory and
find good agreement between the experimental and theoretical data. SCMF calculations show that the segmental interaction energy
between PS matrix chains and APTES is two orders of magnitude stronger than that between PS and SiOx. 相似文献
6.
7.
8.
Russel M. Walters Karen E. Sohn Karen I. Winey Russell J. Composto 《Journal of Polymer Science.Polymer Physics》2002,40(24):2833-2841
The local environment of unneutralized carboxylic acid groups in poly(ethylene‐ran‐methacrylic acid) (E/MAA) ionomers neutralized with monovalent (Li and Na) and divalent (Ca and Zn) ions has been investigated with Fourier transform infrared spectroscopy. These unneutralized acid groups interact with one another to form acid dimers, and they associate with existing neutralized complexes. At room temperature, no free acids can be detected for any system, not even for pure E/MAA. With the acid dimer peak (1700 cm?1) and a known unneutralized acid concentration, the concentration of acids associated with a neutralized complex can be determined. This concentration of associated acids increases with increasing neutralization, reaches a maximum below 50% neutralization, and then decreases toward zero near 80% neutralization. This behavior is perhaps due to the increased driving force for aggregation of the neutralization acids. Although Li, Na, and Ca contain similar concentrations of associated acids over the range of neutralizations, the Zn system contains far fewer associated acids (i.e., more acid dimers) at any particular neutralization level. These results are confirmed by an analysis of the absorbance in the neutralized region (1650–1500 cm?1). © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2833–2841, 2002 相似文献
9.
Deshmukh RD Composto RJ 《Langmuir : the ACS journal of surfaces and colloids》2007,23(26):13169-13173
Direct embedding of metal nanoparticles (NPs) into the surface of a polymer melt is observed by TEM and a new embedding mechanism proposed. Upon annealing above the glass transition temperature of polystyrene (PS), NPs (20 nm gold) are rapidly covered by a thin PS wetting layer, h* approximately 1.3-1.8 nm (i.e., about two or three monomers). Because it creates capillary pressure on a NP, this "universal" wetting layer is proposed to be responsible for NP embedding. The value of h* is independent of the molecular weight of PS and constant during the embedding process. The value of h* is found to be similar to the equilibrium wetting layer thickness of a polymer melt spreading on a metal substrate. Using a model that includes the spreading coefficient, long-range van der Waals interactions, and a chain-stretching penalty, h* is shown to be independent of the molecular weight of the polymer. Using this model and the measured value of h*, the interfacial energy between Au NP and PS is estimated to be 8.7 J/m2. 相似文献
10.
Extensive new high-temperature, high-resolution FTIR emission spectroscopy measurements for the five common isotopomers of GeO are combined with previous diode laser and microwave measurements in combined isotopomer analyses. New Dunham expansion parameters and an accurate analytical potential energy function are determined for the ground X1Sigma+ state. Copyright 1999 Academic Press. 相似文献