Acetate Film (acetate + film)

Distribution by Scientific Domains


Selected Abstracts


Solution-Deposited Zinc Oxide and Zinc Oxide/Pentacene Bilayer Transistors: High Mobility n-Channel, Ambipolar, and Nonvolatile Devices,

ADVANCED FUNCTIONAL MATERIALS, Issue 12 2008
Bhola Nath Pal
Abstract A solution processed n-channel zinc oxide (ZnO) field effect transistor (FET) was fabricated by simple dip coating and subsequent heat treatment of a zinc acetate film. The field effect mobility of electrons depends on ZnO grain size, controlled by changing the number of coatings and zinc acetate solution concentration. The highest electron mobility achieved by this method is 7.2,cm2 V,1 s,1 with On/Off ratio of 70. This electron mobility is higher than for the most recently reported solution processed ZnO transistor. We also fabricated bilayer transistors where the first layer is ZnO, and the second layer is pentacene, a p-channel organic which is deposited by thermal evaporation. By changing the ZnO grain size (or thickness) this type of bilayer transistor shows p-channel, ambipolar and n-channel behavior. For the ambipolar transistor, well balanced electron and hole mobilities are 7.6,×,10,3 and 6.3,×,10,3,cm2 V,1 s,1 respectively. When the ZnO layer is very thin, the transistor shows p-channel behavior with very high reversible hysteresis. The nonvolatile tuning function of this transistor was investigated. [source]


Improvement of light fastness of natural dyes.

COLORATION TECHNOLOGY, Issue 5 2001
Part 2: Effect of functional phenyl esters on the photofading of carthamin in polymeric substrate
The photofading behaviour of carthamin in cellulose acetate film was investigated. A contribution from singlet oxygen to that fading was suggested. Phenyl esters containing nickel sulphonate quenching groups were prepared and the protecting effect of these compounds towards the photofading of carthamin was examined in cellulose acetate film. It is proposed that nickel sulphonate derivatives of phenyl esters can be applied as effective stabilisers against the fading of natural dyes. [source]


Characterization of polycyclic aromatic hydrocarbon bioavailability in estuarine sediments using thin-film extraction

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 5 2007
Christopher J. Golding
Abstract It is well documented that the bioavailability of hydrophobic organic chemicals (HOCs) can vary substantially among sediments. This makes risk assessments based on total sediment concentrations problematic. The present study investigates the application of thin-film solid-phase extraction to measure bioavailable concentrations of phenanthrene in estuarine sediment by comparing concentrations of phenanthrene in the amphipod Corophium colo and in thin ethylene/vinyl acetate films at different concentrations in three geochemically different sediments. For all sediment types, concentrations of phenanthrene in sediments and thin films followed linear relationships, indicating first-order exchange kinetics. Organism/thin-film concentration ratios did not vary systematically among sediment types but dropped significantly with increasing phenanthrene concentration in the sediments. While at low phenanthrene concentrations in the sediment fugacities of phenanthrene in the amphipods approached the fugacities in the thin films, they were significantly lower than those in the sediments at higher concentrations. While phenanthrene concentrations in the three sediment types were identical, biota sediment accumulation factors and concentrations in amphipods and thin films were consistently lower in sediments enriched with black carbon than in sediments with sedimentary organic matter bearing a more diagenetic organic signature. It is concluded that, for the range of concentrations tested, thin-film solid-phase extraction can be a useful tool in the characterization of differences in bioavailability of HOCs among sediment types. [source]


Development of a 1-Methylcyclopropene (1-MCP) Sachet Release System

JOURNAL OF FOOD SCIENCE, Issue 1 2006
Younsuk S. Lee
ABSTRACT The partitioning of 1-methylcyclopropene (1-MCP) between the gas/polymer matrix was determined for 2 adsorbing agents and 4 sachet materials to estimate the adsorption potential of 1-MCP at 23°C. The release study was performed using a closed system under 2 different environmental conditions, dry air (0% RH) and 90% RH. Sachets made from Tyvek®, paper, low-density polyethylene (LDPE), and polyvinyl acetate (PVA) materials were fabricated to contain silica gel and activated carbon. Activated carbon sachets did not release 1-MCP at either testing condition. Activated carbon had a very strong affinity for 1-MCP. The permeability coefficients of 1-MCP and water in polyethylene and polyvinyl acetate films were determined using a quasi-isostatic method. LDPE sachets containing silica gel had similar 1-MCP release rates at both 0% and 90% RH. PVA sachets containing silica gel had slow release of 1-MCP. The amount of 1-MCP released from PVA sachets containing silica gel at 90% RH was larger than the amount of 1-MCP released at 0% RH. Release of 1-MCP from paper and Tyvek sachets was largely dependent on the sorbate-absorbing ability of the adsorbing agents. [source]


Characterization of chitosan/citrate and chitosan/acetate films and applications for wound healing

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008
Junichi Tanigawa
Abstract In this work, we aimed to develop a scaffold of chitosan (CS) with a porous sponge structure for an artificial skin. The scaffolds were prepared from both CS/citric and CS/acetic solutions. In addition, the cast films were also prepared from the same solutions to compare some of their properties. They were characterized using WAXD, FTIR, DSC, tensile measurements, and SEM observation. It was found that CS/acetate had low crystallinity but CS/citrate was in an amorphous state, resulting in a large ductility with rubbery softness. Despite the different morphologies of CS/citrate and CS/acetate scaffolds, both scaffolds exhibited the wound healing effect available for tissue engineering. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]