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Honeycomb Films (honeycomb + film)

Distribution by Scientific Domains

Polymers and Materials Science	100%

Selected Abstracts

Influence of Solvents on the Formation of Honeycomb Films by Water Droplets Templating

MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 5 2006
Ye Tian
Abstract Summary: Several solvents were utilized to investigate their influence on the formation of honeycomb patterns. The polymers PPO, PLGA and PLLGA were dissolved in different solvents or mixed solvents to form porous membranes. It was found that a good compatibility between the polymers and their solvents, and an appropriate volatility of the solvent were beneficial for the formation of regular structures. Moreover, C2HCl3 and CH2Cl2, neither of whose PPO solutions could form regular structures at 30,°C, were mixed at different volume ratios to dissolve PPO and fabricate porous structures. The result showed that a regular pattern was achieved when the volume ratio of C2HCl3:CH2Cl2 was 90:10 and that a special structure with big pores surrounded by small pores was obtained when the volume ratio of C2HCl3:CH2Cl2 was 10:90. Based on these phenomena, possible reasons were also proposed. [source]

Solvent Resistant Honeycomb Films from Photo-Crosslinkable Polycinnamate

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 8 2007
Olaf Karthaus
Abstract Microporous films consisting of two-dimensionally ordered void structures - so-called honeycomb films - were produced by evaporation of polymer solutions under high humidity. Two types of poly(vinyl cinnamate)s were used: A newly synthesized amphiphilic poly(vinyl cinnamate) and a mixture of a commercial poly(vinyl cinnamate) and an amphiphilic polyion complex. Photo-crosslinking of the honeycomb structure could be achieved by UV irradiation while completely retaining the film morphology. The crosslinked films showed excellent stability against organic solvents. [source]

Self-Organized Single-Walled Carbon Nanotube Conducting Thin Films with Honeycomb Structures on Flexible Plastic Films

ADVANCED FUNCTIONAL MATERIALS, Issue 2 2009
Nobuo Wakamatsu
Abstract Complex 1, synthesized from anionic shortened single-walled carbon nanotubes and cationic ammonium lipid dissolved in organic solvents, is cast on pretreated transparent flexible poly(ethylene terephthalate) (PET) films under a higher relative humidity to form thin films with self-organized honeycomb structures. The cell sizes are controllable by changing the experimental conditions. The lipid, which is the cationic part of complex 1, is easily removed by a simple ion-exchange method, while maintaining the basic honeycomb structures. After the ion exchange, the nanotube honeycomb films on PET with thinner skeletons exhibit a dramatic decrease in the surface resistivity from insulating to conducting. Carbon nanotubes with honeycomb structures formed by the self-organization on flexible polymer films are useful in many areas of nanoscience and technology including nanomaterials, nanoelectronics, nanodevices, catalysts, sensors, and so on. [source]

Dramatic Morphology Control in the Fabrication of Porous Polymer Films,

ADVANCED FUNCTIONAL MATERIALS, Issue 22 2008
Luke A. Connal
Abstract Highly ordered, porous honeycomb films are prepared by the breath-figure (BF) technique using dendron-functionalized star polymers as precursors. By changing the nature of the dendritic end groups, dramatically different porous morphologies can be produced. Three series of star polymers are prepared with both the size of the 2,2-bis(methoxy)propionic acid (bis-MPA)-based dendron end group and the dendron functionality being varied. Star polymers end-functionalized with acetonide-protected dendrons (generations 1 to 4) are initially prepared and the acetonide groups subsequently deprotected to yield hydroxyl-functionalized star polymers. Modification of these hydroxyl groups with pentadecafluorooctanoyl chloride yields a third series of functionalized star polymers. The resulting star polymers have surface groups with very different polarity and by utilizing these star polymers to form honeycomb films by the BF technique, the morphology produced is dramatically different. The star polymers with amphiphilic character afford interconnected porous morphologies with multiple layers of pores. The star polymers with pentadecafluorooctanoyl end groups show highly ordered monolayers of pores with extremely thin walls and represent a new porous morphology that has previously not been reported. The ability to prepare libraries of different dendronized star polymers has given further insights into the BF technique and allows the final porous morphology to be controllably tuned utilizing the functional chain ends and generation number of the dendronized star polymers. [source]

Fabrication of Reversibly Crosslinkable, 3-Dimensionally Conformal Polymeric Microstructures,

ADVANCED FUNCTIONAL MATERIALS, Issue 20 2008
Luke A. Connal
Abstract Multifaceted porous materials were prepared through careful design of star polymer functionality and properties. Functionalized core crosslinked star (CCS) polymers with a low glass transition temperature (Tg) based on poly(methyl acrylate) were prepared having a multitude of hydroxyl groups at the chain ends. Modification of these chain ends with 9-anthracene carbonyl chloride introduces the ability to reversibly photocrosslink these systems after the star polymers were self-assembled by the breath figure technique to create porous, micro-structured films. The properties of the low Tg CCS polymer allow for the formation of porous films on non-planar substrates without cracking and photo-crosslinking allows the creation of stabilized honeycomb films while also permitting a secondary level of patterning on the film, using photo-lithographic techniques. These multifaceted porous polymer films represent a new generation of well-defined, 3D microstructures. [source]