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Sea dye marker block releases a visible slick which lasts at least twelve hours. The dye marker uses a fluorescent dye in a heat cured binder which, when immersed in seawater, releases the dye at a controlled rate.
The author has identified the following significant results. For two years ERTS-1 has been employed to investigate current circulation patterns in Delaware Bay under different tidal, flow, and wind conditions. Since sufficient numbers of current meters and boats are not available, air-droppable drogues and dye packs have been developed and tested. The drogues consist of a styrofoam float and a line to which is attached a stainless steel biplane. The length of the line determines at what depth currents will be monitored. The floats are color coded to distinguish their movement and mark the depth of the biplanes. Simultaneously floating and anchored dye packs of fluorescein dye have been deployed from aircraft. The movement of the dye and drogues is tracked by sequential aerial photography, using fixed markers on shore or on buoys as reference points to calibrate the scale and direction of drogue movement. The current data obtained by this technique is then used to annotate current circulation maps derived from ERTS-1 imagery.
A straightforward method for the user of color imagery to determine the spectral analytical density of dyes present in the processed imagery is presented. The method involves exposing a large number of different color patches on the film which span the gamut of the film's imaging capabilities. From integral spectral density measurements at 16 to 19 different wavelengths, the unit spectral dye curves for each of the three dyes present were determined in two different types of color films. A discussion of the use of these spectral dye densities to determine the transformation between integral density measurements and analytical density is presented.
Existing DIAL systems for water vapor measurements in the troposphere operate at wavelengths near 720 nm. The use of stronger water vapor absorption lines in the range 930 to 960 nm will significantly improve DIAL measurements in the upper troposphere and lower stratosphere where water vapor concentrations are low. The generation of light at 940 nm using a frequency doubled Nd:YAG pumped dye laser is inefficient due to the small absorption if infrared dyes at the pump wavelength. However, 940 nm generation utilizing stimulated Raman scattering of dye lasers is attractive because of a potentially high conversion efficiency plus the possibility of retaining the narrow linewidth available from some dye lasers. The Raman conversion efficiency and line broadening are presented for first Stokes operation at 720 and 940 nm using hydrogen and deuterium as the Raman media.
Dye laser gains were measured at various pump-beam irradiances on a dye cell in order to evaluate the feasibility of solar pumping. Rhodamine 6G dye was considered as a candidate for the solar-pumped laser because of its high utilization of the solar spectrum and high quantum efficiency. Measurements show that a solar concentration of 20,000 is required to reach the threshold of the dye.
Threshold solar power for dye laser pumping has been determined by measuring the gain of a rhodamine 6G dye laser amplifier at various solar-simulated irradiances on an amplifier cell. The measured threshold was 20,000 solar constants (2.7 kW/sq cm) for the dye volume of 2 x 5 x 40 cu mm and the optimum dye concentration of 0.001 M. The threshold is about one-third of that achievable with a high-intensity solar concentrator.
A new potential DIAL laser transmitter is described that uses solid-state dye laser materials to make a simpler, more compact, lower mass laser system. Two solid-state dye laser materials were tested to evaluate their performance in a laser oscillator cavity end pumped by a pulsed Nd:YAG laser at 532 nm. The polymer host polymethyl-methacrylate was injected with a pyrromethene laser dye, PM 580, or PM 597. A narrowband laser oscillator cavity was constructed to produce visible wavelengths of 578 and 600 nm which were frequency doubled into the UV region (299 or 300 nm) by using a BBO crystal, resulting in a maximum energy of 11 mJ at a wavelength of 578 nm when pumped by the Nd:YAG laser at an energy of 100 mJ (532 nm). A maximum output energy of 378 microJ was achieved in the UV region at a wavelength of 289 nm but lasted only 2000 laser shots at a repetition rate of 10 Hz. The results are promising and show that a solid-state dye laser based ozone DIAL system is possible with improvements in the design of the laser transmitter.
The present invention discloses a new class of highly fluorescent indicator dyes that are specific for calcium ions. The new fluorescent indicator dyes combine a stilbene-type fluorophore with a tetracarboxylate parent Ca.sup.2+ chelating compound having the octacoordinate pattern of liganding groups characteristic of EGTA and BAPTA. Preferred forms contain extra heterocyclic bridges to reinforce the ethylenic bond of the stilbene and to reduce hydrophobicity. Compared to their widely used predecessor, quin2, the new dyes offer up to thirty-fold brighter fluorescence, major changes in wavelength (not just intensity) upon Ca.sup.2+ binding, slightly lower affinities for Ca.sup.2+, slightly longer wavelengths of excitation, and considerably improved selectivity for Ca.sup.2+ over other divalent cations. These properties, particularly the wavelength sensitivity to Ca.sup.2+, make the dyes useful indicators for many intracellular applications, especially in single cells, adherent cell layers, or bulk tissues. The present invention also discloses an improved method for synthesizing alpha-acyloxyalkyl bromides wherein the bromides so synthesized are free of contaminating bis(1-bromoalkyl)ether. The improved method is exemplified herein in the synthesis of acetoxymethyl bromide, a compound useful in preparing the acetoxymethyl esters disclosed herein as novel Ca.sup.2+ specific fluorescent indicators.
A novel series of hydrophobic room temperature ionic liquids based on six cyclic sulfonium cations were first time synthesized and applied in dye-sensitized solar cells as pure solvents for electrolyte system. The chronoamperograms result showed that the length of substituent on sulfonium cations could inhibit the I{sub 3}{sup -} diffusion and the five-ring structure of sulfonium was benefit for fast triiodide ion diffusion. The electrochemical impendence spectra measurement of dye-sensitized solar cells with these ionic liquid electrolytes was carried out and the result indicated that the cations' structure had indeed influence on the cells' performance especially for the fill factor, which was further proved by the measurement result of I-V curves of these dye-sensitized solar cells. The conclusion was obtained that the electron exchange reaction on Pt counter electrode/electrolyte interface dominated the cells' performance for these ionic liquid electrolyte-based DSCs. (author)
Three organic dyes with D-{pi}-D-{pi}-A structure based on triarylamine, dimethylarylamine, and rhodanine-3-acetic acid moieties are designed and synthesized. Incorporating thiophene moieties into the system affords sensitizers with high molar extinction coefficients. These dyes were applied into nanocrystalline TiO{sub 2} dye-sensitized solar cells through standard operations. For a typical device the maximal monochromatic incident photon-to-current conversion efficiency (IPCE) can reach 73%, with a short-circuit photocurrent density (J{sub sc}) of 7.3 mA/cm{sup 2}, an open-circuit voltage (V{sub oc}) of 636 mV, and a fill factor (ff) of 0.61, corresponding to an overall conversion efficiency ({eta}) of 2.86%. (author)
A novel multi-component biosorbent consisted of pine, oak, hornbeam and fir sawdust biomasses was used to eliminate a common hazardous dye (Malachite green, MG) from aqueous solution. The influences of different parameters like solution pH, biosorbent amount, dye concentration and contact time on the removal process were thoroughly studied to evaluate optimum biosorption conditions. The pseudo-first-order, pseudo-second-order, Elovich, logistic and intra-particle diffusion models were used to describe the biosorption kinetics. Logistic model represented the kinetic experimental data well. The experimental equilibrium biosorption data were analyzed by Freundlich, Langmuir and Dubinin–Radushkevich isotherms. Freundlich model fitted better with the experimental data compared to others. In addition, the mean free energy obtained from Dubinin–Radushkevich model and the standard Gibbs free energy change indicated that the nature of biosorption was feasible, spontaneous and physical type. Overall, the novel eco-biosorbent could be used as a promising biosorbent to remove such unsafe dye molecules from aqueous environments.
A novel superabsorbent hydrogel (SAHs) composed of (acrylic acid, sodium alginate and sodium humate) (AAc/NaAlg/SH) SAHs were tested as adsorbent for metal ions Cu{sup 2+}, Pb{sup 2+}, and Fe{sup 2+} ions as well as MB and CV dyes. The influence of SH concentration varies from 6.97, 8.04, 9.09, 10.11% and 11 wt% were designated as S{sub 1}, S{sub 2}, S{sub 3}, S{sub 4}, S{sub 5}, respectively. The synthesized superabsorbent hydrogel were used for the adsorption of Cu{sup 2+}, Pb{sup 2+}, Fe{sup 2+} and MB and CV dyes from their aqueous solutions. The binding capacity for Cu{sup 2+}, Pb{sup 2+}, Fe{sup 2+} ions were 311 mg/gm/L at 850 mg/L, 209 mg/gm/L at 850 mg/L and 197 mg/gm/L at 850 mg/L for initial ion concentration respectively and MB and CV dyes molecules were 323 mg/gm/L at 360 mg/L, 289 mg/gm/L at 360 mg/L for initial molecule concentration per gram of AAc/NaAlg/SH containing 9.09 wt% SH content. The adsorption data obeyed Langmuir sorption isotherms.
Phase-pure anatase TiO{sub 2} nanocrystallite aggregates synthesized by a continuous supercritical fluid process have been first used for fabricating mesoporous photoanodes of dye-sensitized solar cells (DSCs). Due to the small size (11 nm) of the TiO{sub 2} nanocrystallites in the aggregates, the mesoporous photoanode provides a high specific surface area, 80 m{sup 2}/g, which ensures high dye loading. At the same time, the submicrometer-sized aggregates endow the mesoporous photoanode with strong light scattering effect. Therefore, the light harvesting efficiency of the photoanode is increased. With an improved short-circuit current density, a high overall power conversion efficiency of 8.65% (100 mW/cm{sup 2}, AM 1.5) is achieved without additional scattering layers, 12% enhanced compared with the DSCs fabricated from commercial Degussa P25 with exactly the same procedures. In addition, this supercritical fluid process is scalable and rapid (less than one minute) for TiO{sub 2} aggregates synthesis, which will push the commercialization of DSCs in the future. - Graphical abstract: Due to the special morphology and structure, the photoanode of DSCs provides high specific surface area and strong light scattering at the same time, which results in high conversion efficiencies of the DSCs. Table of contents: Thanks to the synchronous realization of high specific surface area and strong light scattering, a high efficiency of 8.65% was achieved based on a novel mesoporous TiO{sub 2} aggregates photoanode for DSCs. Highlights: Black-Right-Pointing-Pointer The TiO{sub 2} aggregate photoanode provides a possible route for highly efficient DSCs. Black-Right-Pointing-Pointer Photoanode with high dye loading and light scattering is successfully fabricated. Black-Right-Pointing-Pointer TiO{sub 2} synthesized by a supercritical fluid process is first applied to DSCs. Black-Right-Pointing-Pointer The synthesis method and high efficiency will push the commercialization of DSCs.
Graphical abstract: They consist of treating triazoloisoquinolines substituted tetramethyl-dioxaborolane (2) with 5-formyl-2-bromothiophene under conditions for Suzuki coupling to produce 5-(4-(3-oxo-[1,2,4]triazolo[3,4-a]isoquinolin-2(3H)-yl)phenyl) thiophene-2-carbaldehyde (3). Knoevenagel condensation of compound 3 with cyanoacrylic acid is carried out in the presence of piperidine, and after precipitation and purification with silica gel chromatography, the final dyestuff 4L is obtained as a yellow powder. This product has been characterized by spectroscopic analyses. Display Omitted Highlights: ► This new dyestuff investigated the role of triazoloisoquinoline dyestuffs as co-adsorbents and co-sensitizers with N719. ► The results show that co-adsorption of N719 sensitizer with dyestuff 5 increases the photocurrent in 1–0.25 molar ratio. ► This improved conversion efficiency is attributed to the insulating molecular layer, and the light harvesting effect at shorter-wavelength regions. -- Abstract: Triazoloisoquinoline contains electron-rich nitrogen and oxygen heteroatoms in a heterocyclic structure with high electron-donating ability. By utilizing this feature, two organic dyesutffs containing triazoloisoquinoline were synthesized and used in the fabrication of dye-sensitized solar cells (DSSCs), overcoming the deficiency of ruthenium dyestuff absorption in the blue part of the visible spectrum. This method also fills the blanks of ruthenium dyestuff sensitized TiO{sub 2} film, and forms a compact insulating molecular layer due to the nature of small molecular organic dyestuffs. The incident photon-to-electron conversion efficiency of N719 at shorter wavelength regions is 35%. After addition of triazoloisoquinoline-based dyestuff for co-sensitization, the IPCE at 350–500 nm increased significantly. This can be attributed to the increased photocurrent of the cells, which improves the dye-sensitized photoelectric conversion efficiency from 4.49% to 5.15%, which the overall conversion efficiency increased by about 15%. As a consequence, this low molecular weight organic dyestuff is a promising candidate as co-adsorbent and co-sensitizer for highly efficient dye-sensitized solar cells.
Highlights: ► CdSe–graphene is synthesized by hydrothermal method. ► Three molar solutions of CdSe were used making three different composites. ► RhB and Texbrite MST-L were used as sample dye solutions. ► Texbrite MST-L is photo degraded in visible light. ► UV-spectroscopic analysis was done to measure degradation. - Abstract: CdSe–graphene composites were prepared using simple “hydrothermal method” where the graphene surface was modified using different molar solutions of cadmium selenide (CdSe) in aqueous media. The characterization of CdSe–graphene composites were studied by X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscope (SEM), and with transmission electron microscope (TEM). The catalytic activities of CdSe-composites were evaluated by degradation of rhodamine B (RhB) and commercial industrial dye “Texbrite MST-L (TXT-MST)” with fixed concentration. The degradation was observed by the decrease in the absorbance peak studied by UV spectrophotometer. The decrease in the dye concentration indicated catalytic degradation effect by CdSe–graphene composites.
Graphical abstract: - Highlights: • Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres were successfully synthesized by a hydrothermal procedure. • Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres were used to remove wastewater pollutant containing azo dye. • The activity of Bi{sub 2}O{sub 3}/CeO{sub 2} is synergically enhanced compared to its pristine forms. - Abstract: We report on the visible-light responsive porous assembly of Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres, which were synthesized via a simple hydrothermal reaction between Bi(NO{sub 3}){sub 3}·5H{sub 2}O and Ce(NO{sub 3}){sub 3}·6H{sub 2}O in the presence of ethylene glycol and ethanol. Systematic structural (X-ray diffraction (XRD)), morphological (field emission scanning electron microscopy (FE-SEM) and transmission electron microscopic (TEM)), BET surface area and diffuse reflectance spectral (DRS) analyses were carried out to characterize the formed product. The effects of experimental parameters on the microstructural and morphological behavior of Bi{sub 2}O{sub 3}/CeO{sub 2} composites were discussed. The semiconductor material as obtained was evaluated as a heterogeneous photocatalyst for the photolytic degradation of an azo dye in water and the degradation was found to follow pseudo-first-order rate kinetics. The study compares the rate constants of the new hybrid catalyst to a pristine Bi{sub 2}O{sub 3} and CeO{sub 2}, which has excellent catalytic properties under visible light irradiation for the degradation of Orange II dye.
Highlights: • TiO{sub 2} nanorods doped with Ca ions were synthesized by one-step hydrothermal method. • The flat band edge of rutile TiO{sub 2} shifted positively via Ca-doping. • The photoelectric conversion efficiency of dye-sensitized solar cells (DSSCs) based on TiO{sub 2} electrode was much enhanced by Ca-doping. • A relatively high open circuit voltage was obtained by adopting Ca-doped TiO{sub 2} nanorods electrode. - Abstract: Ca-doped TiO{sub 2} nanorod arrays were prepared via the one-step hydrothermal method successfully, and the effect of Ca ions content on the photovoltaic conversion efficiency of dye-sensitized solar cells has been fully discussed in the paper. Although no obvious change on the microstructure and morphology was observed by field emission scanning electron microscope and transmission electron microscope for the Ca-doped samples, the results of X-ray diffraction and X-ray photoelectron spectroscopy confirmed that Ti{sup 4+} was substituted with Ca{sup 2+} successfully. UV–vis spectroscopy results revealed that the flat band edge shifted positively by Ca ions doping. The photovoltaic conversion efficiency of the dye-sensitized solar cells based on the 2 mol% Ca-doped TiO{sub 2} electrode was 43% higher than that of the undoped one due to the less recombination possibility.
Highlights: • Photoelectrode made of Hydrogen titanate nanotubes from H{sub 2}Ti{sub 3}O{sub 7}. • Solar cell efficiency enhancement from 5.95% to 7.63%. • Increase of Voc due to a decrease in the work function on HTNT. • Increase of Jsc due to an increase of the specific area of HTNT. - Abstract: The existent research literature of Dye Sensitized Solar Cells (DSSC) is mainly focused on the dye but there are very few studies focused in the semiconductor. Here, we present the performance of hydrogen titanate nanotubes (HTNT), showing an enhancement of the solar cell efficiency from 5.95% to 7.63%, respect to anatase as photoelectrode. This enhancement could be explained in terms of open-circuit voltage, directly associated to the value of the HTNT band gap (E{sub g} = 3.3 eV), the relative position of the edge conduction band; and the increase of the short-circuit current, directly associated to the enhancement of the specific area of the photoelectrode. All these characteristics are in very good concordance with our theoretical modelling of the system, based on First Principles calculations. We expect that this system could be further characterized, utilizing different dyes or absorbers, in order to evaluate the potential use of hydrogen titanate nanotubes for solar cell applications.