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The relationship between damage mechanisms and energy absorption up to failure was revealed.
Different initial water contents and evolution of water absorption up to 28 days were analyzed.
Relative to their phenylene analogues 46 48, these series showed red shifted absorption (up to 10 nm).
The FIR absorption up to ∼400 μm for AlGaAs films with different Al fractions and doping are presented.
This simple relation for the sound absorption up to now was derived from individual solutions for finite-size absorbers, only.
The outcomes exhibited significant porosity of > 80%, moderate degradation rate, and tremendous value of water absorption up to 1163% in all samples.
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They are soluble in polar organic solvents and insoluble in water, but show equilibrium water absorptions up to 21.0% by wt.
Absorption grades 1 and 4 showed high absorption capacity (up to 8%%) while it was in the range of 3%% for grade 2 and 5.
The parasitic phase of (Bi/Fe 2O3 in BiFeO3 synchronously makes its a clearly red shift of light absorption edge up to approximately 665 nm, enhanced visible-light absorption, and improved charge separation due to their suitable bands positions and intimate contact.
The deposited layer of CdS nanoparticles sensitizes the TiO2 surface to visible light; CdS-sensitized TiO2 IO films demonstrate absorption of up to approximately 550 nm light, with enhanced absorption for increased CdS deposits.
In addition, those systems can only measure absorption coefficients up to 0.3 mm−1, not high enough to measure the absorption coefficient of whole blood in the VIS/NIR spectral range.
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