Direct-to-video holographic readout in quantum wells for three-dimensional imaging through turbid media

Customized photorefractive quantum-well devices have been developed for real-time video acquisition of coherence-gated, three-dimensional images in turbid media. Large-field-of-view holographic imaging with direct video capture is now possible. We have evaluated the role of intensity-limited device performance in Fourier-plane and image-plane holography in such devices and, using near-infrared light, have imaged through turbid phantoms of 13 mean free paths' scattering depth with 50-microm transverse and 60-microm depth resolution.     

Interfacial polycondensation. II. Fundamentals of polymer formation at liquid interfaces

If a solution of a fast-reacting diacid halide in a water-immiscible solvent is brought together with an aqueous solution of a diamine without stirring, a thin film of high polymer is formed at once at the interface. Polyurethanes and polyamides in. particular form tough films which can be grasped and pulled continuously from the interface as a folded rope of film. The unstirred interfacial polycondensation not only provides a dramatic demonstration of polymer formation but has permitted the observation of polymerization behavior and the study of the effects of many variables upon the process. The polymer-forming reactions proceed by nucleophilic displacement, and many have rate constants of at least 10²–10¹ l. mole^-1 sec.^-1. Polymers derived from diamines were found to form in the organic solvent phase. Therefore the rate of polymer formation is controlled by the transfer of diamine from the aqueous phase. It is believed that the liquid interface does not have any beneficial orienting effect on the reactants but that it provides for the regulated flow of one reactant into an excess of the other. Furthermore, the aqueous phase provides for the removal of the interfering byproduct, hydrogen halide, from the polymerization site. Some of the interrelated variables which have been studied and which are discussed in relation to the physical mechanism are the solvent sensitivity of the polymer, partition coefficients of the reactants, reactant concentration, duration of the polymerization, and the addition of the monofunctional reactants, detergents, and salts. The formation of polyphenyl esters is discussed briefly.     

The Mechanism of Adsorption of Rh(III) Bromide Complex Ions on Activated Carbon

In the paper, the mechanism of the process of the Rh(III) ions adsorption on activated carbon ORGANOSORB 10—AA was investigated. It was shown, that the process is reversible, i.e., stripping of Rh(III) ions from activated carbon to the solution is also possible. This opens the possibility of industrial recovery of Rh (III) ions from highly dilute aqueous solutions. The activation energies for the forward and backward reaction were determined These are equal to c.a. 7 and 0 kJ/mol. respectively. Unfortunately, the efficiency of this process was low. Obtained maximum load of Rh(III) was equal to 1.13 mg per 1 g of activated carbon.     

The onset of coulomb explosions in polyatomic molecules

With the development of high intensity femtosecond lasers, the ionisation and dissociation dynamics of molecules has become an area of considerable interest. Using the technique of femtosecond laser mass spectrometry (FLMS), the molecules carbon disulphide, pyrimidine, toluene, cyclohexanone and benzaldehyde are studied with pulse widths of 50 fs in the near infrared (IR) wavelength region (790 nm). Results are presented and contrasted for laser beam intensities around 10(15) and 10(16) W cm(-2). For the lower intensities, the mass spectra yield dominant singly charged parent ions. Additionally, the appearance of doubly charged parent ions is evident for carbon disulphide, toluene and benzaldehyde with envelopes of doubly charged satellite species existing in these local regions. Carbon disulphide also reveals a small triply charged component. Such atomic-like features are thought to be a strong fingerprint of FLMS at these intensities. However, upon increasing the laser intensity to approximately 10(16) W cm(-2), parent ion dominance decreases and the appearance of multiply charged atomic species occurs, particularly carbon. This phenomenon has been attributed to Coulomb explosions in which the fast absorption of many photons may produce transient highly ionised parent species which can subsequently blow apart. Copyright 1999 John Wiley & Sons, Ltd.     

Uniform molecular analysis using femtosecond laser mass spectrometry

The potential of femtosecond laser time-of-flight mass spectrometry (FLMS) for uniform quantitative analysis of molecules has been investigated. Various samples of molecular gases and vapours have been studied, using ultra-fast ( approximately 50 fs) laser pulses with very high intensity (up to 1.6 x 10(16) Wcm(-2)) for non-resonant multiphoton ionisation/tunnel ionisation. Some of these molecules have high ionisation potentials, requiring up to ten photons for non-resonant ionisation. The relative sensitivity factors (RSF) have been determined as a function of the laser intensity and it has been demonstrated that for molecules with very different masses and ionisation potentials, uniform ionisation has been achieved at the highest laser intensities. Quantitative laser mass spectrometry of molecules is therefore a distinct possibility. Copyright 1999 John Wiley & Sons, Ltd.     

Rhodamine 6G conjugated to gold nanoparticles as labels for both SERS and fluorescence studies on live endothelial cells

Microchimica Acta - Fluorescence and surface-enhanced Raman scattering (SERS) spectroscopy were employed to investigate the cellular uptake of rhodamine 6G (R6G) alone and of R6G loaded with gold...     

Adsorption isotherms of homologous alkyldimethylbenzylammonium bromides on sodium montmorillonite

The adsorption of homologous alkyldimethylbenzylammonium bromides, [C(6)H(5)CH(2)N(CH(3))(2)R]Br, on sodium montmorillonite from aqueous NaCl solutions at room temperature has been studied. R stands for the methyl-, butyl-, hexyl-, octyl-, decyl-, and dodecyl-group, and the corresponding ammonium cations will be denoted as C1+, C4+, C6+, C8+, C10+, and C12+, respectively. C1+, the reference cation, attains the plateau region of adsorption at a level close to the cation exchange capacity (CEC) of the clay. The chain-length dependence on adsorptivity of the homologous cations exhibits an unexpected peculiarity. In the case of short-chain homologues of C1+ their adsorption onto sodium montmorillonite decreases in the order C1+>C4+>C6+. This behavior is due, presumably, to the growing steric hindrances at the surface of clay, which occur because of the limited area available for the bulky organic cations at the exchange sites. These limitations appear to be out-balanced in the case of higher homologues for which the increasingly growing hydrophobic effects lead to the expected sequence of adsorptivity of the cations, i.e., C1+相似文献   

Orthophosphoric acid solutions of sodium orthovanadate,sodium tungstate,and sodium molybdate as potential corrosion inhibitors of the Al2Cu intermetallic phase

Orthophosphoric acid solutions of sodium orthovanadate, sodium tungstate, and sodium molybdate are tested as potential corrosion inhibitors of the Al₂Cu intermetallic phase. Corrosion inhibition is observed for 0.2 M solutions of Na₃VO₄ and Na₂WO₄ by increasing the pH to > 2. When the pH is < 2, the aforementioned salts increase the corrosion rate of the intermetallic phase. A 0.2 M solution of Na₃VO₄ causes the precipitation of vanadium phosphate on the surface of the Al₂Cu phase at pH = 1.