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221.
Price KK McCormick AV Francis LF 《Langmuir : the ACS journal of surfaces and colloids》2012,28(28):10329-10333
Nonuniformities, such as heavy edges or "coffee rings", frequently develop as particulate coatings dry. One idea for avoiding these nonuniformities is to engineer the substrate edges. In this work, monodisperse latex coatings were deposited on substrates with photoresist walls around their edges. Cryogenic scanning electron microscopy (cryoSEM) results show particle accumulation near the walls and at the free surface. The contact line, pinned at the wall, generates lateral transport of water and particles, leading to a nonuniform coating thickness. Still, coatings on substrates with walls were shown to have a higher degree of thickness uniformity after drying than those without walls. 相似文献
222.
Basu SK McCormick AV Scriven LE 《Langmuir : the ACS journal of surfaces and colloids》2006,22(13):5916-5924
An in-plane constrained cross-linked gel layer absorbs an equilibrium amount of solvent and experiences in-plane compressive stress. A stability analysis of such an elastic gel layer that is attached to either a viscous or an elastic bottom layer atop a rigid substrate is considered. The effects of the top and bottom layer moduli (E(t) and E(b)), the bottom-to-top layer thickness ratio (H/h), and the polymer solvent interaction parameter (chi) on the critical condition of wrinkling, wrinkle wavelength, and amplitude are examined. When the bottom layer is viscous, the compressed top layer is always unstable, and wrinkling is rate-controlled. The viscous flow of the bottom layer governs the rate and determines the fastest growing wavelength. As E(t) rises, the bending stiffness of the elastic layer does as well, and so the fastest growing wavelength (lambda(m)) rises and the equilibrium amplitude (A(e)) falls. As H/h rises, the constraint of the rigid substrate diminishes, and so lambda(m) and A(e) rise. As chi falls or as the solvent has higher affinity for the polymeric gel, lambda(m) falls and A(e) rises because better solvents create higher compressive strain that promote low-wavelength, high-amplitude wrinkles. When the bottom layer is elastic, a critical compressive stress exists. If the generated compressive stress by solvent absorption is greater than the critical stress, the top layer wrinkles. It was found that wrinkling is most likely at intermediate E(t), low E(b), high H/h, and low chi. Further, lower chi, higher H/h, and lower E(b) were found to promote higher equilibrium amplitude and higher wavelength wrinkles. 相似文献
223.
To develop viable polymer stabilized liquid crystal systems, it is crucial to understand the factors that affect polymer nanostructure evolution. This work examines the influence of the photopolymerization of aliphatic and fluorinated monoacrylate monomer within a room temperature smectic liquid crystal (LC). Additionally, the effect of LC order on polymerization kinetics, monomer and polymer organization, and the effect of the polymer on LC properties have been examined. Through this work, insight has been gained regarding the impact that the introduction of a fluorinated monoacrylate monomer has on polymerization kinetics, LC organization, and monomer/polymer segregation and organization within a polymer/LC system. Fluorinated moieties lower the surface energy of the monomer to enhance segregation between the smectic layers of the LC as compared with an analogous aliphatic monomer. Additionally, the enhanced segregation significantly increases the polymerization rate in the smectic phase and drives the continued segregation of the fluorinated polymer during and after polymerization. Fluorination also leads to the formation of an ordered polymer nanostructure if polymerized in ordered LC phases. This ordering is particularly evident when the fluorinated monomer is polymerized in the smectic phase in which the monomer is organized between the smectic layers of the LC. In addition, the ordered polymer structure found with the fluorinated monomer in the smectic phase leads to continued birefringence above the clearing point of the LC due to surface interactions between the LC and the ordered fluorinated polymer. The continued birefringence offers an exceptional opportunity to examine how factors such as polymer molecular mass and UV light intensity affect the overall polymer morphology of these polymer/LC systems. As the initiator concentration and UV light intensity are decreased, longer polymer chains form lattice-type morphologies; whereas, shorter polymer chains form smoother morphologies that more closely mirror the texture of the LC smectic phase. 相似文献
224.
To develop viable polymer stabilized liquid crystal systems, it is crucial to understand the factors that affect polymer nanostructure evolution. This work examines the influence of the photopolymerization of aliphatic and fluorinated monoacrylate monomer within a room temperature smectic liquid crystal (LC). Additionally, the effect of LC order on polymerization kinetics, monomer and polymer organization, and the effect of the polymer on LC properties have been examined. Through this work, insight has been gained regarding the impact that the introduction of a fluorinated monoacrylate monomer has on polymerization kinetics, LC organization, and monomer/polymer segregation and organization within a polymer/LC system. Fluorinated moieties lower the surface energy of the monomer to enhance segregation between the smectic layers of the LC as compared with an analogous aliphatic monomer. Additionally, the enhanced segregation significantly increases the polymerization rate in the smectic phase and drives the continued segregation of the fluorinated polymer during and after polymerization. Fluorination also leads to the formation of an ordered polymer nanostructure if polymerized in ordered LC phases. This ordering is particularly evident when the fluorinated monomer is polymerized in the smectic phase in which the monomer is organized between the smectic layers of the LC. In addition, the ordered polymer structure found with the fluorinated monomer in the smectic phase leads to continued birefringence above the clearing point of the LC due to surface interactions between the LC and the ordered fluorinated polymer. The continued birefringence offers an exceptional opportunity to examine how factors such as polymer molecular mass and UV light intensity affect the overall polymer morphology of these polymer/LC systems. As the initiator concentration and UV light intensity are decreased, longer polymer chains form lattice-type morphologies; whereas, shorter polymer chains form smoother morphologies that more closely mirror the texture of the LC smectic phase. 相似文献
225.
2 + Na2S → CdS + 2NaCl induced by mechanical milling resulted in the formation of CdS particles with an average diameter of < 8 nm.
The average particle size was controlled within the range of 4 to 8 nm by varying the size of the grinding media. The onset
energy of optical absorption showed a blue shift with decreasing particle size.
Received: 29 August 1997/Accepted: 25 September 1997 相似文献
226.
C. Bizon M. D. Shattuck John R. de Bruyn J. B. Swift W. D. McCormick Harry L. Swinney 《Journal of statistical physics》1998,93(3-4):449-465
Motions of individual particles within the stripe and square patterns formed in oscillated granular media are studied using numerical simulations. Our event-driven molecular dynamics simulations yield standing wave patterns in good accord with those observed in experiments at the same frequency and acceleration amplitude. The patterns are subharmonic and so return to their initial macroscopic state after two external cycles. However, simulations reveal that individual particles do not return to their initial position. In addition to diffusive motion, an organized flow of particles within the patterns is found; associated with each peak and each valley of the pattern is a pair of counterrotating convection rolls. The diffusion is anisotropic: transport perpendicular to stripes is enhanced over that parallel to stripes. This enhancement is computed as a function of the layer depth, acceleration amplitude, frequency, and coefficient of restitution of the particles, and is attributed to the effect of the advective motion. Velocity distributions, granular temperature, and the dependence of the diffusion coefficient parallel to the stripes on the average granular temperature are studied. 相似文献
227.
Michael J. Fevola Matthew G. Kellum Roger D. Hester Charles L. McCormick 《Journal of polymer science. Part A, Polymer chemistry》2004,42(13):3252-3270
The solution properties of low‐charge‐density ampholytic terpolymers of acrylamide, sodium 3‐acrylamido‐3‐methylbutanoate, and (3‐acrylamidopropyl)trimethylammonium chloride were studied as functions of the solution pH, ionic strength, and polymer concentration. Terpolymers with low charge densities, large charge asymmetries, or both exhibited excellent solubility in deionized (DI) water, and higher charge density terpolymers were readily dispersible in DI water; however, the higher charge density terpolymer solutions separated into polymer‐rich and polymer‐poor phases upon standing over time. Charge‐balanced terpolymers exhibited antipolyelectrolyte behavior at pH values greater than or equal to the ambient pH (6.5 ± 0.2); the same terpolymers behaved increasingly as cationic polyelectrolytes with decreasing solution pH because of the protonation of the 3‐acrylamido‐3‐methylbutanoate (AMB) repeat units. Unbalanced terpolymers generally exhibited polyelectrolyte behavior, although the effects of intramolecular electrostatic attractions (i.e., polyampholyte effects) on the hydrodynamic volume of the unbalanced terpolymer coils were evident at certain values of the solution pH and salt concentration. The dilute‐solution behavior of the terpolymers correlated well with the behavior predicted by several polyampholyte solution theories. In the semidilute regime, solution viscosities increased with increasing terpolymer charge density, and this indicated a significant enhancement of the solution viscosity by intermolecular electrostatic associations. Upon the addition of NaCl, semidilute‐solution viscosities tended to decrease because of the disruption of the intermolecular electrostatic associations. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3252–3270, 2004 相似文献
228.
Danagoulian A Mamyan VH Roedelbronn M Aniol KA Annand JR Bertin PY Bimbot L Bosted P Calarco JR Camsonne A Chang CC Chang TH Chen JP Choi S Chudakov E Degtyarenko P de Jager CW Deur A Dutta D Egiyan K Gao H Garibaldi F Gayou O Gilman R Glamazdin A Glashausser C Gomez J Hamilton DJ Hansen JO Hayes D Higinbotham DW Hinton W Horn T Howell C Hunyady T Hyde CE Jiang X Jones MK Khandaker M Ketikyan A Kubarovsky V Kramer K Kumbartzki G Laveissière G Lerose J Lindgren RA Margaziotis DJ Markowitz P 《Physical review letters》2007,98(15):152001
Cross-section values for Compton scattering on the proton were measured at 25 kinematic settings over the range s=5-11 and -t=2-7 GeV2 with a statistical accuracy of a few percent. The scaling power for the s dependence of the cross section at fixed center-of-mass angle was found to be 8.0+/-0.2, strongly inconsistent with the prediction of perturbative QCD. The observed cross-section values are in fair agreement with the calculations using the handbag mechanism, in which the external photons couple to a single quark. 相似文献
229.
We have measured -3.5 dB (-8.1 dB corrected for losses) relative intensity squeezing between probe and conjugate beams generated by stimulated, nondegenerate four-wave mixing in hot rubidium vapor. Unlike early observations of squeezing in atomic vapors based on saturation of a two-level system, our scheme uses a resonant nonlinearity based on ground-state coherences in a three-level system. Since this scheme produces narrowband, squeezed light near an atomic resonance, it is of interest for experiments involving cold atoms or atomic ensembles. 相似文献
230.
McAllister LA McCormick RA James KM Brand S Willetts N Procter DJ 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(4):1032-1046
A fluorous, cyclative-capture strategy based on a new Pummerer cyclization process allows rapid access to tagged, heterocyclic frameworks. Convenient modification of the fluorous, heterocyclic scaffolds by using a variety of approaches including Pd-catalyzed cross-couplings is possible. Traceless, reductive cleavage of the fluorous-phase tag or oxidative cleavage and further elaboration, completes a strategy for the high-throughput, fluorous-phase synthesis of a diverse range of N-heterocycles. 相似文献