Search NASA⌕ Search

SEARCH · Search NASA

Results for “RHODAMINES”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 19 records

Effective dose and persistence of Rhodamine-B in wild pig Vibrissae

Due to substantial ecological and economic damage attributed to wild pigs (Sus scrofa), there is international interest in using pharmaceutical baits to control populations. To assess the efficacy and specificity of baiting programs, one may use chemical biomarkers to evaluate uptake of pharmaceutical baits. In particular, Rhodamine B (RB) is known to be an effective biomarker in wild pigs. However, significant data gaps exist regarding the minimum effective dosage and the persistence of RB in wild pigs. To investigate this we used a controlled double-blind study, administering a one-time dose of RB at three treatment levels (5, 15, or 30 mg/kg) to 15 pigs, with five pigs per treatment group. Facial vibrissae were collected pre-RB ingestion as a control and every 2 weeks post-RB ingestion for 12 weeks. We examined samples for RB presence and used a generalized linear mixed model (GLMM) to determine the influence of treatment dose on persistence of RB. Additionally, we measured distance moved by the RB mark away from the vibrissae root and used a GLMM to assess movement rates of RB bands along growing vibrissae. Here, we found consistently greater persistence of RB in the 15 and 30 mg/kg treatments across the sampling period (p = 0.005 and p = <0.0001, respectively). A significant, positive movement trend in RB bands was observed within the 15 and 30mg/kg groups. Based on our results, a 15 mg/kg dosage can be considered a minimum effective dose for wild pigs and will reliably produce a detectable RB mark up to and likely beyond 12 weeks post-ingestion.

59 BASIC BIOLOGICAL SCIENCES↗

Rationalizing the suitability of rhodamines as chromophores in dye-sensitized solar cells: A systematic molecular design study

Here, rhodamines are chromophores that are employed in many dye applications. Their strong optical absorption in the visible region of the electromagnetic spectrum renders them attractive dye candidates for dye-sensitized solar cells (DSCs). However, they have not yet been systematically tested in DSCs as single- or co-sensitizers. Recent advances in concerted experimental and computational workflows involving molecular design protocols can afford a better understanding of the molecular origins of the optoelectronic properties in these sensitizers. Herein, we examine the suitability of rhodamines R560 (1), R575 (2), R590 (3), R610 (4), R620 (5), R640 (6), and R3B (7) as chromophores in co-sensitized DSCs. Our study follows a stepwise approach. Initially, structural and optical properties of the dyes are investigated by experimental and computational methods to reveal structure-property relationships and other useful features for DSC applications. Subsequently, 1-7 are investigated at the dye···TiO 2 interface, both by calculations of dye-adsorption onto the surface of a modeled (TiO 2 ) 9 cluster, and by experimental studies of dye-adsorption on TiO 2 . For that purpose, a selection of rhodamine dyes are paired together (1 and 5) and (1 and 7) for co-sensitization, among which 5 is also co-adsorbed with a fluorescein dye in order to explore chemical compatibility factors. The best dye candidates are identified from the findings of these adsorption studies in terms of dye aggregation, anchoring modes, and panchromatic response. Despite their promising dye…TiO 2 adsorption and optical prospects, our results show that rhodamines lack a suitable intramolecular charge transfer pathway for dye-to-TiO 2 electron injection to occur, thus precluding their photovoltaic function as DSC dyes. Our results are then assessed against ostensibly disparate reports of rhodamines performing successfully in DSC devices; this comparison necessitated the internal reproduction of previously reported co-sensitization experiments on 2 with the industrial standard reference dye, N3. We achieve reconciliation between our results and those in the literature by reasoning that while rhodamines cannot deliver photovoltaic function in DSCs in their own right, they can either act to facilitate or deplete the photovoltaic output of a DSC indirectly by affecting the TiO 2 adsorption prospects of a photovoltaic-active dye with which a rhodamine is co-sensitized.

14 SOLAR ENERGY↗

Coumarin-Rhodamine Hybrids—Novel Probes for the Optical Measurement of Viscosity and Polarity

A comprehensive systematic study of absorption and fluorescence properties in solvents of varying viscosity and polarity of three novel and red-emitting coumarin-rhodamine hybrid derivatives with differences in the rigidity of their substituents is presented. This includes ethanol-polyethylene glycol, toluene-polyethylene glycol, and toluene-paraffin mixtures. Moreover, protonation-induced effects on the spectroscopic properties are studied. A viscosity-induced emission enhancement was observed for all coumarin-rhodamine hybrid derivatives. MCR2 bearing a julolidine donor showed the expected low sensitivity to viscosity whereas MCR3 with its freely rotatable diphenylamino substituent revealed a particularly pronounced sensitivity to this parameter. Moreover, MCR2 shows an enhancement in emission in the open, i.e., protonated form in conjunction with a largely Stokes shift fluorescence in the deep red spectral region. This enables the application of these dyes as viscosity sensors and as far red emitting pH-sensitive probes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Facile synthesis of gold nanopuncheons with high-index facets and their SERS effects on Rhodamine 6G

Highlights: • Au nanopuncheons with high-index facets have been prepared by seed-mediated growth. • The nanopuncheons are enclosed by 24 planes of (2 5 0), (3 0 1) and 2 (0 1 0) planes. • The nanopuncheons showed high SERS activity toward Rhodamine 6G. - Abstract: Au nanopuncheons with exposed high-index facets have been synthesized in high-yield by employing didodecyldimethylammonium bromide (DDAB) as surfactant in one-step seed-mediated growth. Transmission electron microscopy (TEM) characterization showed that the as-prepared Au nanopuncheons possessed 24 high index facets of (2 5 0), (3 0 1), and 2 (0 1 0) planes. Due to the high density of atomic steps and kinks in the structure, the Au nanopuncheons exhibited high surface enhanced Raman scattering (SERS) activity toward Rhodamine 6G.

36 MATERIALS SCIENCE↗

Synthesis of Tb{sub 4}O{sub 7} complexed with reduced graphene oxide for Rhodamine-B absorption

Highlights: • Tb–rGO composite was fabricated via a facile thermally reduction process. • The green and blue emissions were both observed in the composite. • The composite exhibited efficient absorption capability for Rhodamine-B. - Abstract: Tb{sub 4}O{sub 7} complexed with reduced graphene oxide composite (Tb–rGO) had been designed and fabricated by a facile thermal reduction method. The formation of Tb{sub 4}O{sub 7} particles and reduction of graphene oxide (GO) occurred simultaneously, and partial terbium ions would be complexed with rGO via oxygen-containing function groups on rGO sheets. Introducing of terbium ions could effectively tune the photoluminescence properties of rGO, and the composite exhibited the typical green emission of terbium ions as well as the blue self-luminescence of graphene entered at 440 nm. Moreover, Tb–rGO had demonstrated its high capability as an organic dye (Rhodamine-B) scavenger with high speed and efficiency. The findings showed the promising applications for large-scale removal of organic dye contaminants, especially in the field of waste water treatment.

36 MATERIALS SCIENCE↗

Stimulated emission from aluminium anode oxide films doped with rhodamine 6G

The spectral and luminescent properties of the rhodamine 6G dye in a porous matrix of aluminium anode oxide are studied. The films with a highly-ordered porous structure are produced using the method of two-stage anodic oxidation. By means of raster electron microscopy it is found that the diameter of the pores amounts to nearly 50 nm and the separation between the adjacent channels is almost 105 nm. The thickness of the films is equal to 55 μm, and the specific surface area measured using the method of nitrogen capillary condensation is 15.3 m{sup 2} g{sup -1}. Fluorescence and absorption spectra of rhodamine 6G molecules injected into the pores of the aluminium anode oxide are measured. It is found that under the excitation of samples with the surface dye concentration 0.3 × 10{sup 14} molecules m{sup -2} by the second harmonic of the Nd : YAG laser in the longitudinal scheme with the pumping intensity 0.4 MW cm{sup -2}, a narrow band of stimulated emission with the intensity maximum at the wavelength 572 nm appears against the background of the laser-induced fluorescence spectrum. A further increase in the pumping radiation intensity leads to the narrowing of the stimulated emission band and an increase in its intensity. The obtained results demonstrate the potential possibility of using the porous films of aluminium anode oxide, doped with laser dyes, in developing active elements for quantum electronics. (laser applications and other topics in quantum electronics)

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Study of the deposition features of the organic dye Rhodamine B on the porous surface of silicon with different pore sizes

The deposition features of the organic dye Rhodamine B on the porous surface of silicon with average pore sizes of 50–100 and 100–250 nm are studied. Features of the composition and optical properties of the obtained systems are studied using infrared and photoluminescence spectroscopy. It is found that Rhodamine-B adsorption on the surface of por-Si with various porosities is preferentially physical. The optimal technological parameters of its deposition are determined.

36 MATERIALS SCIENCE↗

Investigating Single-Molecule Fluorescence Spectral Heterogeneity of Rhodamines Using High-Throughput Single-Molecule Spectroscopy

We experimentally investigated several intra-molecular coordinate and environmental changes as potential causes of single-molecule fluorescence spectral heterogeneities (smFSH). Here, we developed a high-throughput single-molecule spectroscopy technique to analyze more than 5,000 single-molecule emission spectra from each of nine commonly used fluorophores with different structural rigidities deposited on substrates with different polarities. We observed an unexpected high smFSH from structurally rigid Rhodamine B compared with a structurally flexible Cyanine dye - Alexa Fluor 647. Based on experimentally measured smFSH, we ruled out the system’s noise uncertainty, single-molecule spectral diffusion, and environmental polarity as the primary causes of the high smFSH. We found that the rotational flexibility of N, N-dialkylated groups contributed to the smFSH. With the high smFSH observed in structurally more rigid model fluorophores, we speculated that other intra-molecular coordinate and environmental changes might also contribute to the high smFSH in Rhodamines.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Two-photon-excited fluorescence resonance energy transfer in an aqueous system of CdTe quantum dots and Rhodamine B

Two-photon excited fluorescence resonance energy transfer (FRET) between CdTe quantum dots with different emission peaks and Rhodamine B in aqueous solution are investigated both experimentally and theoretically. The photoluminescence and lifetime are measured using a time-resolved fluorescence test system. The two-photon excited FRET efficiency is found to increase as the degree of spectral overlap of the emission spectrum of CdTe and the absorption spectrum of Rhodamine B increases, which is due to the increase of Forster radius of the sample. Moreover, FRET efficiency increases when the ratio of acceptor/donor concentration increases. The two-photon excited FRET efficiency was found to reach 40%.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Determination of Cerium (IV) Using Rhodamine 6G Fluorescence Quenching

The interaction between rhodamine 6G (Rh6G) and cerium sulfate was studied by the fluorescence quenching method. In a sulfuric acid medium, the interaction of Ce(IV) with Rh6G results in Rh6G fluorescence quenching. The maximum excitation wavelength (λ{sub ex}) and the maximum emission wavelength (λ{sub em}) are 530 nm and 555 nm, respectively. A good linearity between the relative fl uorescence intensity (ΔF) and Ce(IV) was observed in the range ~0.12–1.08 μg/mL. The detection limit was 1.4 × 10{sup –3} μg/mL. The optimum reaction conditions, influencing factors, and effect of coexisting substances were investigated in the experiment. We found that the concentration of Rh6G was 3.2 × 10{sup –6} mol/L, and the fl uorescence intensity was maximum.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Adsorption of Methylene Blue, Brilliant Green and Rhodamine B from Aqueous Solution Using Collagen-g-p(AA-co-NVP)/Fe{sub 3}O{sub 4}@SiO{sub 2} Nanocomposite Hydrogel

In this study, the collagen-g-poly(acrylic acid-co-N-vinylpyrrolidone)/Fe{sub 3}O{sub 4}@SiO{sub 2} (collagen-g-p(AA-co-NVP)/Fe{sub 3}O{sub 4}@SiO{sub 2}) as magnetic nanocomposite hydrogel was synthesized by graft copolymerization of acrylic acid (AA) and N-vinylpyrrolidone (NVP) onto collagen in the presence of the Fe{sub 3}O{sub 4}@SiO{sub 2} using ammonium persulfate as a free radical initiator and bis[2-(methacryloyloxy)ethyl] phosphate as a crosslinker under ultrasound-assisted condition. The blank collagen-g-p(AA-co-NVP) hydrogel and its composite with the Fe{sub 3}O{sub 4}@SiO{sub 2} nanoparticles were characterized by means of FTIR, SEM-EDS, XRD, VSM and TGA methods. The effects of different parameters such as pH, dose of adsorbent and time on swelling behavior were examined. The swelling ratio of the collagen-g-p(AA-co-NVP) hydrogel increased in the presence of the Fe{sub 3}O{sub 4}@SiO{sub 2} nanoparticles. Adsorption behavior of magnetic nanocomposite hydrogel was investigated for the adsorption of dyes and it was found to remove about 93% for methylene blue, 96% for brilliant green and 89% for rhodamine B in 50 mg/L of dyes solutions at pH 7. Kinetic study revealed the applicability of pseudo-first-order and pseudo-second-order models for the adsorption of mentioned dyes. The adsorption isotherm was studied in 25, 35, 45 and 55 °C using Langmuir, Freundlich, Temkin and Sips models and the adsorption data were well described by Langmuir isotherm model. Negative values of ΔG{sup º} for all three dyes suggested the feasibility of dyes removal and support for spontaneous adsorption of mentioned dyes on magnetic nanocomposite hydrogel. Desorption of dyes from the dye loaded nanocomposite hydrogel was simply done in ethanol. The results indicate that the prepared magnetic nanocomposite hydrogel is an efficient adsorbent with high adsorption capacity for the aforementioned dyes.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Mil-100(Fe) nanoparticles supported on urchin like Bi{sub 2}S{sub 3} structure for improving photocatalytic degradation of rhodamine-B dye under visible light irradiation

Highlights: • Facile synthesis a new hybrid photocatalyst MIL-100(Fe)@Bi{sub 2}S{sub 3}. • Investigation enhanced photocatalytic performance of MIL-100(Fe)@Bi{sub 2}S{sub 3} compared to individual components. • Determination the main active species during photocatalytic degradation of RhB over MIL-100(Fe)@Bi{sub 2}S{sub 3}. • Propose photocatalytic mechanism for degradation of RhB over MIL-100(Fe)@Bi{sub 2}S{sub 3}. - Abstract: Metal organic framework (MOFs) have been attracted a great attention as a new type photocatalysts due to their unique properties. In this work, the new hybrid photocatalyst based on fabrication hybrid structures between MIL-100(Fe) and Bi{sub 2}S{sub 3} (MIL-100(Fe)@Bi{sub 2}S{sub 3}) were synthesized via simple hydrothermal method. The photocatalytic degradation of Rhodamine B (RhB) over the as-prepared samples showed that the hybrid photocatalyst samples had higher photocatalytic performance compared to the individual components (MIL-100(Fe) and Bi{sub 2}S{sub 3}). The higher photocatalytic performance of the hybrid photocatalysts was proved by electrochemical and photoelectrochemical analysis such as electrochemical impedance spectroscopy (EIS) and also photocurrent measurement. In addition, the possible photocatalytic mechanism based on the optical, photoelectrochemical and quenching tests was proposed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

BODIPY modified g-C{sub 3}N{sub 4} as a highly efficient photocatalyst for degradation of Rhodamine B under visible light irradiation

Highlights: • Post modification strategy to reduce the residual amine on the g-C{sub 3}N{sub 4} frameworks through Schiff base reaction using BODIPY derivatives was adopted. • Reinforced visible light absorption and depressed carrier recombination were seen in the post modified photocatalysts. • Photocatalytic performance of modified photocatalysts were strengthened by more than 3.5 times than the pure g-C{sub 3}N{sub 4}. - Abstract: Developing new energy resource as well as efficient treatment strategies to solve the energy crisis and organic pollutants problems is of crucial importance. Due to medium band gap and highly thermal stability, doped or chemically functionallized graphitic carbon nitride (g-C{sub 3}N{sub 4}) has been envisioned as promising photocatalysts in processing organic pollutants. In this work, we use 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) chemically modified g-C{sub 3}N{sub 4} to degrade Rhodamine B (RhB) under visible light irradiation (λ ≥ 420 nm). When the modified weight ratio of BODIPY in g-C{sub 3}N{sub 4} reaches 0.6% (CN-0.6), the photocatalytic performance is nearly 3.5 times fast than that of without modification (CN-0). Enhanced visible light absorption and depressed electron-hole recombination rate may take responsibilities for the enhanced photocalytic performance. A possible mechanism responsible for this photocatalytic process is proposed. Our work might provide a new strategy to develop valid photocatalysts with broad visible light absorption.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Growth, microstructure, structural and optical properties of PVP-capped CdS nanoflowers for efficient photocatalytic activity of Rhodamine B

Highlights: • Synthesis of un-capped and PVP-capped CdS microstructures by Hydrothermal. • Growth of both the flower and dendrite microstructures controlled by the growth time. • Phase transition of CdS from cubic zinc blend to hexagonal by the growth time. • CdS flowers enhanced the photocatalytic performance of RhB under visible light. • PVP-capped CdS showed the highest degradation of 95% of RhB within 120 min. - Abstract: Size and structure tunability of polyvinyl pyrolidone (PVP) capped cadmium sulfide (PVP-capped CdS) flowers were synthesized by controlling the reaction time. XRD pattern indicated a phase transition from the cubic zinc blend to the hexagonal phase of CdS powder as the reaction time increased. As per the microstructure analysis with respect to the reaction time, the spherical nanoparticles were transformed in to the flower like morphology consisting of sword like nanorods and confirmed by the bright field images of TEM, while, HR-TEM images showed the uniform lattice spacing. UV-spectra exhibited a red shift due to the excitations of CdS nanoparticles. The near band edge (NBE) peak of PVP-capped CdS was completely diminished which indicated to sulphur vacancies on the surface of flowers. The photocatalytic activity of PVP-capped CdS flowers was detected the fast degradation of Rhodamine B (RhB) dye (95% for 120 min) by irradiation of visible light.

36 MATERIALS SCIENCE↗

Raspberry—like monodispersity ZnO microspheres for photodegradation of rhodamine B

Highlights: • Rasberry-like ZnO microspheres were successfully prepared through a F108-assisted one-pot hydrothermal route. • The resulting ZnO microspheres are composed of many small nanoparticles, generating a unique rough surface. • The surface rough and the diameter of the microspheres can be easily tuned only by changing the composition of the precursor. • The Au decorated-ZnO composite demonstrates better photocatalytic activities for degradation of RhB than the pristine ZnO micropheres. - Abstract: In the article, we propose a simple and effective one-pot hydrothermal approach for synthesis of raspberry-like ZnO microspheres, where triblockpoly (ethylene oxide)-poly (propylene oxide)-poly (ethylene oxide), triethanolamine, ethylene glycol acts as the structure-directing agent (SDA), co-template, and solvent, respectively. They are together responsible for the growth of ZnO products with uniform morphology, high crystallinity, and good monodispersity. The resulting ZnO microspheres possess rough surface, which are composed of many small nanoparticles. Moreover, the surface roughness and the diameter of the microspheres can be easily tuned only by changing the composition of the precursor. Meanwhile, the photodegradation behavior of the products is also tested by selecting the rhodamine B (RhB) as the model pollutant. The photocatalytic results indicate that the raspberry-like ZnO products exhibit excellent photocatalytic activity. In particular, the Au decorated-ZnO composite demonstrates an enhanced photocatalytic activity towards degradation of RhB under UV irradiation compared with the pristine ZnO microspheres.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Fabrication of In2O3/TiO2 nanotube arrays hybrids with homogeneously developed nanostructure for photocatalytic degradation of Rhodamine B

Highlights: • A new class of plate-like In{sub 2}O{sub 3}/TNAs photocatalyst is successfully fabricated. • The obtained In{sub 2}O{sub 3}/TNAs hybrid presents a well-aligned nanotubular structure. • In{sub 2}O{sub 3} particles are dispersed homogeneously on TNAs without blocking the nozzles. • In{sub 2}O{sub 3}/TNAs hybrid shows a much enhanced Rhodamine B degradation efficiency. • In{sub 2}O{sub 3}/TNAs hybrid demonstrates an excellent recycling capability. - Abstract: To enhance the photocatalytic recycling capability of the TiO{sub 2}-based photocatalysts, a new kind of plate-like In{sub 2}O{sub 3}/TiO{sub 2} nanotube array (TNA) hybrids is fabricated herein by constructing TNAs via an anodization method followed by doping In{sub 2}O{sub 3} via a solvothermal method. The obtained In{sub 2}O{sub 3}/TNA hybrid demonstrates a well-aligned nanotubular structure with homogeneous dispersion of In{sub 2}O{sub 3} nanoparticles. It shows a much higher degradation rate of 77% after 2 h compared to TNA (37%). In addition, the plate-like feature endows the photocatalysts with an excellent recycling capability. These superior photocatalytic degradation performances can be ascribed to the following factors: (1) the enhanced light absorption ability and efficient separation of photoexcited electron-hole pairs derived from the formation of the heterostructure between the interface of TiO{sub 2} and In{sub 2}O{sub 3}; (2) the efficient transport of reactant molecules provided by the well-defined TNAs and the homogeneous distribution of the In{sub 2}O{sub 3} nanoparticles without blocking the nanotubes.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Three-dimensional MoO3 nanoflowers assembled with nanosheets for rhodamine B degradation under visible light

Highlights: • The orthorhombic three-dimensional MoO{sub 3} nanoflowers were synthesized by the modified hydrothermal method. • Using different amount of HCl to transfer from the h-MoO{sub 3} to the α-MoO{sub 3} was well discussed. • Better pore sizes and surface areas of the three-dimensional MoO{sub 3} nanoflowers accelerate the photodegradation process of RhB. • The three-dimensional MoO{sub 3} nanoflowers showed the photocatalytic activity (91.57%). • This methodology should be useful for preparing other nanostructured catalysts. - Abstract: Three-dimensional hierarchical nanoflowers self-assembled with the orthorhombic molybdenum oxide (α-MoO{sub 3}) nanoflowers were synthesized by the modified hydrothermal method. The structure characterizations of the three-dimensional α-MoO{sub 3} nanoflowers were carried out by scanning electron microscope (SEM), Energy Disperse Spectroscopy (EDS), X-ray diffraction (XRD) and nitrogen adsorption-desorption measurement. Moreover, the three-dimensional α-MoO{sub 3} nanoflowers as photocatalyst exhibited enhanced photocatalytic activity towards photodegradation of Rhodamine B (RhB) under xenon (Xe) lamp irradiation. The results of SEM, EDS, XRD and nitrogen adsorption-desorption measurement showed the three-dimensional α-MoO{sub 3} nanoflowers have a better morphology, pore size (7.99 nm) and surface areas (50.788 m{sup 2} g{sup −1}) than hexagonal MoO{sub 3} (h-MoO{sub 3}) nanosheets, photocatalytic activity studies confirmed that the three-dimensional α-MoO{sub 3} nanoflowers photocatalyst exhibits a high visible-light-driven activity for photodegradation of RhB solution of 91.57% within 160 min under Xe lamp irradiation. A mechanism was also proposed for the degradation of RhB by three-dimensional α-MoO{sub 3} nanoflowers.

77 NANOSCIENCE AND NANOTECHNOLOGY↗