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Optical Absorbance (optical + absorbance)

Distribution by Scientific Domains

Polymers and Materials Science	60%

Selected Abstracts

Scintillation properties of lead tungstate crystals doped with the monovalent ion lithium

PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 13 2004
Yanlin Huang
Abstract Lithium-doped PbWO4 crystals have been grown by the Czochralski method. Optical absorbance, X-ray excited luminescence, light yield measurements and X-ray pulsed excited decays have been investigated. Li+ doping has a very good uniformity and could enhance the luminescence of PbWO4, give some contributions to the "fast" decay components. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]

On the kinetics of voltage formation in purple membranes of Halobacterium salinarium

FEBS JOURNAL, Issue 19 2000
Richard W. Hendler
The kinetics of the bacteriorhodopsin photocycle, measured by voltage changes in a closed membrane system using the direct electrometrical method (DEM) of Drachev, L.A., Jasaitus, A.A., Kaulen, A.D., Kondrashin, A.A., Liberman, E.A., Nemecek, I.B., Ostroumov, S.A., Semenov, Yu, A. & Skulachev, V.P. (1974) Nature249, 321,324 are sixfold slower than the kinetics obtained in optical studies with suspensions of purple membrane patches. In this study, we have investigated the reasons for this discrepancy. In the presence of the uncouplers carbonyl cyanide m -chlorophenylhydrazone or valinomycin, the rates in the DEM system are similar to the rates in suspensions of purple membrane. Two alternative explanations for the effects of uncouplers were evaluated: (a) the ,back-pressure' of the ,µ,H+ slows the kinetic steps leading to its formation, and (b) the apparent difference between the two systems is due to slow major electrogenic events that produce little or no change in optical absorbance. In the latter case, the uncouplers would decrease the RC time constant for membrane capacitance leading to a quicker discharge of voltage and concomitant decrease in photocycle turnover time. The experimental results show that the primary cause for the slower kinetics of voltage changes in the DEM system is thermodynamic back-pressure as described by Westerhoff, H.V. & Dancshazy, Z. (1984) Trends Biochem. Sci.9, 112,117. [source]

Photoresponsive Ferroelectric Liquid-Crystalline Polymers

ADVANCED FUNCTIONAL MATERIALS, Issue 1 2007
P. Beyer
Abstract The photoresponse of ferroelectric smectic side-chain liquid-crystalline (LC) polymers containing a photoisomerizable azobenzene derivative as a covalently linked photochromic side group is investigated. By static measurements in different photostationary states, the effect of trans,cis isomerization on the material's phase-transition temperatures and its ferroelectric properties (spontaneous electric polarization PS and director tilt angle ,) are analyzed. It turns out that the Curie temperature (transition SC* to SA) can be reversibly shifted by up to 17,°C. The molecular mechanism of this "photoferroelectric effect" is studied in detail using time-resolved measurements of the dye's optical absorbance, the director tilt angle, and the spontaneous polarization, which show a direct response of the ferroelectric parameters to the molecular isomerization. The kinetics of the thermal reisomerization of the azo dye in the LC matrix are evaluated. A comparison to the reisomerization reaction in isotropic solution (toluene) reveals a faster thermal relaxation of the dye in the LC phase. [source]

Stability of poly(3,4-ethylene dioxythiophene) materials intended for implants,

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2010
Elin M. Thaning
Abstract This study presents experiments designed to study the stability of the conducting polymer poly(3,4-ethylene dioxythiophene) (PEDOT), under simulated physiological conditions using phosphate-buffered saline (PBS) and hydrogen peroxide (H2O2) (0.01M) at 37°C over a 5- to 6-week period. Voltage pulsing in PBS was used as an additional test environment. The influence of switching the counter ion used in electropolymerization from polystyrene sulphonate (PSS) to heparin was investigated. Absorbance spectroscopy and cyclic voltammetry were used to evaluate the material properties. Most of the samples in H2O2 lost both electroactivity and optical absorbance within the study period, but PEDOT:PSS was found slightly more stable than PEDOT:heparin. Polymers were relatively stable in PBS throughout the study period, with around 80% of electroactivity remaining after 5 weeks, disregarding delamination, which was a significant problem especially for polymer on indium tin oxide substrates. Voltage pulsing in PBS did not increase degradation. The counter ion influenced the time course of degradation in oxidizing agents. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 2010 [source]

Structure and Properties of CdS/Regenerated Cellulose Nanocomposites

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 10 2005
Dong Ruan
Abstract Summary: Novel inorganic-organic hybrid materials composed of cadmium sulfide (CdS) semiconducting nanocrystals and regenerated cellulose (RC) were prepared by using in situ synthesizing method. Cellulose was dissolved in a 6 wt.-% NaOH/4 wt.-% urea/thiourea aqueous solution at low temperature followed by addition of cadmium chloride (CdCl2), resulting that the CdS nanocrystals were successfully grown in situ in the cellulose solution. Nanocomposite films containing homogeneous CdS nanoparticles were obtained by casting the resulting solution. Their structure and optical properties were characterized by X-ray photoelectron spectroscopy, wide-angle X-ray diffraction, thermogravimetry analysis, dynamic mechanical analysis, atomic force microscopy, transmittance electronic microscope, UV-vis spectroscopy, and photoluminescence spectroscopy. The experimental results confirmed that the CdS nanocrystalline existed in the composite films, and cellulose matrix provided a confined medium for CdS particle growth in uniform size. The CdS/RC composites showed narrow emission in photoluminescence spectra, and their optical absorbance in the UV range was higher than that of the cellulose film without CdS. This work provided a simple method to prepare cellulose functional materials in NaOH/urea aqueous solution. Photoluminescence of CdS/RC nanocomposites and TEM image of CdS nanocrystals dispersed in RC matrix. [source]