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Sample records for carmine organic dyes

  1. [Asthma and allergy due to carmine dye].

    PubMed

    Tabar, A I; Acero, S; Arregui, C; Urdánoz, M; Quirce, S

    2003-01-01

    Cochineal carmine, or simply carmine (E120), is a red colouring that is obtained from the dried bodies of the female insect Dactylopius coccus Costa (the cochineal insect). We have evaluated the prevalence of sensitization and asthma caused by carmine in a factory using natural colouring, following the diagnosis of two workers with occupational asthma. The accumulated incidence of sensitization and occupational asthma due to carmine in this factory are 48.1% and 18.5% respectively, figures that make the introduction of preventive measures obligatory. Occupational asthma caused by inhaling carmine should be considered as a further example of the capacity of certain protein particles of arthropods (in this case cochineal insects) to act as aeroallergens. Carmine should be added to the list of agents capable of producing occupational asthma, whose mechanism, according to our studies, would be immunological mediated by IgE antibodies in the face of diverse allergens of high molecular weight, which can vary from patient to patient. Nonetheless, given the existence of different components in carmine, it cannot be ruled out that substances of low molecular weight, such as carminic acid, might act as haptenes. Besides, since we are dealing with a colouring that is widely used as a food additive, as a pharmaceutical excipient and in the composition of numerous cosmetics, it is not surprising that allergic reactions can appear both through ingestion and through direct cutaneous contact. We find ourselves facing a new example of an allergen that can act through both inhalation and digestion, giving rise to an allergolical syndrome that can show itself clinically with expressions of both respiratory allergy and alimentary allergy. PMID:13679965

  2. The history, chemistry and modes of action of carmine and related dyes.

    PubMed

    Dapson, R W

    2007-08-01

    Carmine has been used in biological staining to demonstrate selectively nuclei, chromosomes or mucins, depending on the formulation. Throughout its history in science, complaints and frustrations have been expressed about dye quality. Inconsistencies in dye quality or identity have prevented thorough understanding of staining mechanisms and have caused many stain solutions to behave unsatisfactorily. The aim of this review is to (1) detail causes of these problems, which are rooted in history, geography and production, (2) offer ways to minimize problems and (3) provide modern explanations for stain behavior. Carmine is a "semi-synthetic" dye, i.e., a complex of aluminum and the natural dye cochineal (carminic acid). Carmine shows considerable batch-to-batch variability. Geography, politics, history, agricultural practices and iconography all contribute to the variability of cochineal. In addition, widely divergent manufacturing methods are used to produce carmine. Also, confusion in terminology has led to mislabeling. Pressure from the food industry for a more satisfactory colorant for acidic foods led to the introduction of a new dye, aminocarminic acid, which could enter the biological market inadvertantly. Improved methods of analysis should help the certification process by the Biological Stain Commission. Further standardization could be achieved by replacing most of the methods of solubilizing carmine. The majority of these methods use heat, which is likely to damage the dye molecule. Fortunately, carmine is readily dissolved by raising the pH of the aqueous solvent above 12, and a new form of the dye, now available commercially, is soluble in water without the need for heat or pH adjustment. Chemical structures and physical properties of carminic acid, carmine, aminocarminic acid and kermesic acid are reviewed. A new configuration for carmine is proposed, as well as possible changes to carminic acid and carmine molecules as a result of decomposition caused

  3. Removal of acidic indigo carmine textile dye from aqueous solutions using radiation induced cationic hydrogels.

    PubMed

    Sari, Müfrettin Murat

    2010-01-01

    This study examined the removal of acidic indigo carmine dyes from aqueous solutions using cationic hydrogels. Irradiated hydrogels were investigated as a new sorbent for dye removal from aqueous solution. Poly(N,N-Diethylamino ethyl methacrylate) [poly(DEAEMA)] hydrogels were prepared by radiation polymerisation of N,N-diethylamino ethyl methacrylate [DEAEMA] monomer in the presence of cross-linking agent, ethylene glycol dimethacrylate [EGDMA], and used for the removal of acidic indigo carmine textile dye. The adsorption of dyes was examined using a batch sorption technique. The effects of pH, time and initial dye concentration on the adsorption capacity of hydrogels were investigated. Maximum gelation ratio was 98.2% at irradiation dose of 5.3 kGy. Maximum equilibrium volume swelling, V/V(0), value was 21.3 at pH 2.8. Maximum amount of adsorbed indigo carmine onto hydrogels was 96.7 mg dye/g gel at pH 2.8, 21 h of adsorption time and 120 mg/L initial dye solution. Swelling and adsorption capacity increased with decreasing of pH. Compared with Congo red, amounts of adsorbed indigo carmine are much higher than those of Congo red. Langmuir isotherm model was the best fit for these poly(DEAEMA) hydrogels-indigo carmine systems.

  4. Red cochineal dye (carminic Acid): its role in nature.

    PubMed

    Eisner, T; Nowicki, S; Goetz, M; Meinwald, J

    1980-05-30

    Carminic acid, the well-known red dyestuff from cochineal insects (Dactylopius spp.), is a potent feeding deterrent to ants. This deterrency may be indicative of the natural function of the compound, which may have evolved in cochineals as a chemical weapon against predation. The behavior of an unusual predator is described-the carnivorous caterpillar of a pyralid moth (Laetilia coccidivora)-which is undeterred by carminic acid and feeds on cochineals. The animal has the remarkable habit of utilizing the ingested carminic acid for defensive purposes of its own. PMID:17779027

  5. Indigo Carmine Dye-Polymer Nanocomposite Films For Optical Limiting Applications

    NASA Astrophysics Data System (ADS)

    Sreeja, S.; Mayadevi, S.; Suresh, S. R.; Frobel, P. G. Louie; Smijesh, N.; Philip, Reji; Muneera, C. I.

    2011-10-01

    Nanocomposite films of an organic dye-polymer (Indigo Carmine-PVA) system were fabricated and their optical limiting behaviour was investigated under excitation with 532 nm laser pulses of 5 ns temporal width using the open aperture Z-scan technique. The samples displayed optical limiting behavior under the experimental conditions. The Atomic Force Microscopic (AFM) analysis of the surface topography revealed homogeneous distribution of nanoclustered aggregates grown within the polymer matrix and an average roughness of ˜2.02 nm for the surface. The estimated values of the effective nonlinear absorption coefficient, βeff (˜10-7-10-8 cm/W) marked up to the highest reported ones in literature in the nanosecond regime. The results indicate that these nanocomposite films are potential materials for optical limiting devices used for the protection of human eyes and other delicate optical sensors from laser induced optical damage.

  6. Occupational asthma and immunologic responses induced by inhaled carmine among employees at a factory making natural dyes.

    PubMed

    Quirce, S; Cuevas, M; Olaguibel, J M; Tabar, A I

    1994-01-01

    Carmine is a natural red dye widely used as a food coloring agent and for cosmetic manufacture. It is extracted from the dried females of the insect Dactylopius coccus var. Costa (cochineal). Although it has been reported that inhalation of carmine may give rise to occupational asthma and extrinsic allergic alveolitis, there is little evidence of its immunogenic capacity. We studied nine current employees at a factory making natural dyes and one former employee who had left this plant after occupational asthma developed. A current employee had work-related symptoms of rhinitis and asthma that were confirmed by bronchial provocation tests, and another worker had rhinitis. Immunologic sensitization to carmine and cochineal was evaluated by means of skin testing and determination of serum-specific IgE and IgG subclass antibodies by RAST and ELISA, respectively. The specificity of the RAST assay was investigated by RAST inhibition with different fractions of carmine. The three workers with respiratory symptoms had positive skin prick test reactions to both carmine and cochineal. An immediate response to the bronchial provocation test with carmine and cochineal was observed in the current employee with asthma. Specific IgE antibodies against carmine and cochineal were found only in this worker. RAST inhibition studies indicated that the main allergen had a molecular weight between 10 and 30 kd. Specific IgG antibodies against carmine and cochineal, mainly the subclasses IgG1, IgG3, and IgG4, were found in the 10 subjects surveyed. These findings suggest that carmine may induce immunologic responses, most likely IgE mediated in workers with symptoms of occupational asthma. PMID:8308181

  7. Charge-Transfer Complexation at Carminic Acid-CdS Interface and Its Impact on the Efficiency of Dye-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Shahzad, Naila; Shah, Syed Mujtaba; Munir, Shamsa; Hana, Amina; Jabeen, Uzma; Nosheen, Erum; Habib, Banafsha; Khan, Arif Ullah; Hassan, Zubair; Siddiq, Muhammad; Hussain, Hazrat

    2015-04-01

    We report for the first time charge-transfer complex formation at the interface of carminic acid and cadmium sulfide (CdS) nanoparticles. The complex formation was confirmed by ultraviolet-visible (UV-vis) and fluorescence emission spectroscopy. Cadmium sulfide nanoparticles were synthesized by the wet chemical method and characterized by UV-vis spectroscopy, x-ray diffraction and transmission electron microscopy. Carminic acid, in different concentrations, was chemisorbed on the surface of CdS nanoparticles. Grafting of carminic acid on CdS was confirmed by Fourier transform infrared spectroscopy. Energy levels of the highest occupied molecular orbitals and lowest unoccupied molecular orbitals (LUMO) of both carminic acid and CdS nanoparticles matched well for the injection of electron from LUMO of carminic acid to the conduction band of cadmium sulfide. The photoactive nanohybrid material was used in dye-sensitized solar cells. The efficiency of carminic acid functionalized CdS nanoparticles was found to be double the value obtained for the reference device and remained constant over a certain concentration range owing to the complex formation at the interface. However, raising the concentration of carminic acid beyond 2.5 × 10-5 M resulted in a decrease in efficiency. This was ascribed to charge recombination due to the presence of ungrafted carminic acid molecules.

  8. Effective photocatalytic decolorization of indigo carmine dye in Moroccan natural phosphate-TiO2 aqueous suspensions

    NASA Astrophysics Data System (ADS)

    Naciri, Nouâma; Farahi, Abdelfettah; Rafqah, Salah; Nasrellah, Hamid; El Mhammedi, Moulay Abderrahim; Lançar, IbnToumaret; Bakasse, Mina

    2016-02-01

    Heterogeneous photocatalysis is a significant green technology for application in water purification. In this study, the photocatalytic activity of NP-TiO2 based on Moroccan natural phosphate (NP) doped by titanium dioxide TiO2 was evaluated by photocatalytic decolorization of indigo carmine (IC) dye in aqueous solution as a model pollutant under UV light. The NP-TiO2 catalyst was characterized by XRD, FTIR and surface area. The effect of the calcination temperature of NP-TiO2, catalyst concentration, initial concentration of the IC, initial pH, initial hydrogen peroxide H2O2 concentration and coexisting ions on the photocatalytic decolorization of IC was investigated. The NP-TiO2 showed a significantly higher rate of degradation of IC, when compared to TiO2. After 125 min of irradiation using a low intensity of UV-lamp (15 W ∗ 3 lamps = 45 W), 99% of IC solution (20 mg L-1) was decolorized with 0.5 g L-1 of the NP-TiO2 calcined at 600 °C at pH = 11. Therefore, this process can be developed as an economically feasible and environmentally friendly method to decolorize or treat dye wastewater using sunlight.

  9. Raman spectroscopy of organic dyes adsorbed on pulsed laser deposited silver thin films

    NASA Astrophysics Data System (ADS)

    Fazio, E.; Neri, F.; Valenti, A.; Ossi, P. M.; Trusso, S.; Ponterio, R. C.

    2013-08-01

    The results of a surface-enhanced Raman scattering (SERS) study performed on representative organic and inorganic dyes adsorbed on silver nanostructured thin films are presented and discussed. Silver thin films were deposited on glass slides by focusing the beam from a KrF excimer laser (wavelength 248 nm, pulse duration 25 ns) on a silver target and performing the deposition in a controlled Ar atmosphere. Clear Raman spectra were acquired for dyes such as carmine lake, garanza lake and brazilwood overcoming their fluorescence and weak Raman scattering drawbacks. UV-visible absorption spectroscopy measurements were not able to discriminate among the different chromophores usually referred as carmine lake (carminic, kermesic and laccaic acid), as brazilwood (brazilin and brazilein) and as garanza lake (alizarin and purpurin). SERS measurements showed that the analyzed samples are composed of a mixture of different chromophores: brazilin and brazilein in brazilwood, kermesic and carminic acid in carmine lake, alizarin and purpurin in garanza lake. Detection at concentration level as low as 10-7 M in aqueous solutions was achieved. Higher Raman intensities were observed using the excitation line of 632.8 nm wavelength with respect to the 785 nm, probably due to a pre-resonant effect with the molecular electronic transitions of the dyes.

  10. Matrix-assisted laser desorption and electrospray ionization mass spectrometry of carminic acid isolated from cochineal

    NASA Astrophysics Data System (ADS)

    Maier, Marta S.; Parera, Sara D.; Seldes, Alicia M.

    2004-04-01

    Carminic acid, isolated from cochineal, was analyzed by matrix-assisted laser desorption/ionization (MALDI) and electrospray mass spectrometry (ESI-MS). Application of both techniques to the analysis of carminic acid suspended in linseed oil and applied to a piece of canvas, demonstrated the ability of MALDI and ESI-MS to identify this organic dye in a mixture as those used in easel painting.

  11. Carmine hypersensitivity masquerading as azithromycin hypersensitivity.

    PubMed

    Greenhawt, Matthew; McMorris, Marc; Baldwin, James

    2009-01-01

    Macrolide hypersensitivity is a rarely reported event. However, carmine dye has become increasingly important as a provocative agent. We present a case of a woman with documented carmine hypersensitivity, who reported anaphylaxis 90 minutes after ingestion of a generic azithromycin. Our investigations revealed that this was an allergy to the carmine dye in the tablet's coating rather than to the antibiotic. Seven extracts were prepared including carmine dye, crushed dried female cochineal insects, crushed tablets of Zithromax (Pfizer Inc.) and generic azithromycin (Teva Pharmaceuticals), and the crushed colored coatings from both tablets. These were suspended in preservative-free normal saline, and then applied as a skin-prick test and read at 30 minutes. The skin-prick skin test results were 4+ to histamine and carmine dye, but negative to cochineal insect extract, Pfizer crushed tablets, and negative control. The patient was 1+ to the Teva crushed tablet, but was 4+ to the Teva brand coating and negative to the Pfizer brand coating, which did not contain carmine. The patient subsequently ingested Pfizer Zithromax without any sequelae. To our knowledge, this is the first reported case of carmine anaphylaxis attributed to carmine-containing medication. Careful history and skin-prick testing to the appropriate agents allowed elucidation of the subtlety of the true offending agent without unnecessary avoidance of the medication class. Patients with a carmine hypersensitivity should actively check with their pharmacy or prescribing physician to verify their medications are free of this offending agent. PMID:19331724

  12. Preparation of mesoporous poly (acrylic acid)/SiO2 composite nanofiber membranes having adsorption capacity for indigo carmine dye

    NASA Astrophysics Data System (ADS)

    Xu, Ran; Jia, Min; Li, Fengting; Wang, Hongtao; Zhang, Bingru; Qiao, Junlian

    2012-03-01

    Mesoporous poly (acrylic acid)/SiO2 (PAA/SiO2) composite nanofiber membranes functionalized with mercapto groups were fabricated by a sol-gel electrospinning method, and their adsorption capacity for indigo carmine was investigated. The membranes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, x-ray powder diffraction (XRD), and nitrogen adsorption-desorption measurement. SEM and TEM observation results showed that the PAA/SiO2 fibers had diameters between 400-800 nm and mesopores with an average pore size of 3.88 nm. The specific surface area of the mesoporous nanofiber membranes was 514.89 m2/g. The characteristic peaks for mercapto group vibration in FTIR and Raman spectra demonstrated that the mercapto groups have been incorporated into the silica skeleton. The adsorption isotherm data of indigo carmine on the membranes fit well with Redlich-Peterson model, and the maximum adsorption capacity calculated was 523.11 mg/g. It was found that the removal rate of indigo carmine by the membranes reached a maximum of 98% in 90 min and the adsorption kinetics followed a pseudo-second-order model. The high adsorption capacity of PAA/SiO2 nanofiber membrane makes it a promising adsorbent for indigo carmine removal from the wastewater.

  13. A method for determining identity and relative purity of carmine, carminic acid and aminocarminic acid.

    PubMed

    Dapson, Rw

    2005-01-01

    Carmine is one of the few dyes currently certified by the Biological Stain Commission that is not assayed for dye content. Existing assay methods are complex and do not differentiate the three cochineal derivatives carmine, carminic acid and aminocarminic acid. The latter dye is relatively new to the food trade as an acid-stable red colorant and may eventually enter the biological stains market. The assay proposed here is a two-step procedure using quantitative spectrophotometric analysis at high pH (12.5-12.6) followed by a qualitative scan of a low pH (1.90-2.10) solution. Carmine is distinct at high pH, and the remaining dyes are easily distinguished at low pH. Four instances of mislabeling are documented from 18 commercial products, but the mislabeled dyes were not certified dyes. Samples from nearly all lots of carmine certified by the Biological Stain Commission from 1920 to 2004 proved to be carmine, but they varied widely in dye content. Batches from 1920 through the 1940s were significantly richer in dye content. Variability has been extreme since 2000, and most of the poorest lots have been submitted since 1990. PMID:16720520

  14. A method for determining identity and relative purity of carmine, carminic acid and aminocarminic acid.

    PubMed

    Dapson, Rw

    2005-01-01

    Carmine is one of the few dyes currently certified by the Biological Stain Commission that is not assayed for dye content. Existing assay methods are complex and do not differentiate the three cochineal derivatives carmine, carminic acid and aminocarminic acid. The latter dye is relatively new to the food trade as an acid-stable red colorant and may eventually enter the biological stains market. The assay proposed here is a two-step procedure using quantitative spectrophotometric analysis at high pH (12.5-12.6) followed by a qualitative scan of a low pH (1.90-2.10) solution. Carmine is distinct at high pH, and the remaining dyes are easily distinguished at low pH. Four instances of mislabeling are documented from 18 commercial products, but the mislabeled dyes were not certified dyes. Samples from nearly all lots of carmine certified by the Biological Stain Commission from 1920 to 2004 proved to be carmine, but they varied widely in dye content. Batches from 1920 through the 1940s were significantly richer in dye content. Variability has been extreme since 2000, and most of the poorest lots have been submitted since 1990.

  15. Carminic acid dye from the homopteran Dactylopius coccus hemolymph is consumed during treatment with different microbial elicitors.

    PubMed

    Hernández-Hernández, Fidel de la Cruz; de Muñoz, Fernando García-Gil; Rojas-Martínez, Alberto; Hernández-Martínez, Salvador; Lanz-Mendoza, Humberto

    2003-09-01

    The activation of Dactylopius coccus (Costa) hemolymph with microbial polysaccharide molecules was studied. Hemolymph incubated in the presence of laminarin, zymosan, and N-acetyl glucosamine produced a dark fibrillar precipitated, and the red pigment (carminic acid) was consumed (measured spectrophotometrically at 495 nm). Lipopolysaccharide (LPS) did not induce any response. The reaction was inhibited with millimolar concentrations of serine and cysteine protease inhibitors, EGTA and phenyl thiourea. It was also diminished by prostaglandin synthesis inhibitors: dexamethasone, acetylsalicylic acid, and indomethacin. However, Mg2+ chelator EDTA did not inhibit hemolymph activation. Hemolymph proteins were depleted from soluble phase during treatment with laminarin, but a group of around 34 kDa remained unmodified. These results showed that D. coccus hemolymph is activated by microbial elicitors, its activation depends on eicosanoids, and suggest participation of a prophenoloxidase (PPO)-like activation system that could consume carminic acid. We are currently dissecting the molecular factors involved in D. coccus hemolymph activation to determine homologies and differences with other arthropods immune response pathways. PMID:12942514

  16. The removal of the indigo carmine dye from aqueous solutions using cross-linked chitosan: evaluation of adsorption thermodynamics using a full factorial design.

    PubMed

    Cestari, Antonio R; Vieira, Eunice F S; Tavares, Andréa M G; Bruns, Roy E

    2008-05-01

    A 2(3) factorial design was employed to evaluate the quantitative removal of the indigo carmine (IC) dye from aqueous solutions on glutaraldehyde cross-linked chitosan. The variables were chitosan masses of 100 and 300 mg, IC concentrations of 2.0 and 5.0 x 10(-5) mol L(-1) and temperatures of 25 and 35 degrees C. The quantitative and energetic adsorption parameters were analyzed statistically using modeling with bilinear equations. The results indicated that increasing the chitosan mass from 100 to 300 mg decreases the IC adsorption/mass ratio (mol g(-1)) whereas a temperature increase of 25-35 degrees C increases it. The principal effect of the IC concentration did not show statistical significance. The factorial experiments demonstrate the existence of a significant antagonistic interaction effect between the chitosan mass and temperature. The adsorption thermodynamic parameters, namely Delta(ads)H, Delta(ads)G, and Delta(ads)S, were determined for all the factorial design results. Endothermic values were found in relation to the Delta(ads)H. The positive Delta(ads)S values indicate that entropy is a driving force for adsorption. The Delta(ads)G values are also significantly affected by important antagonistic and synergistic effects involving all principal and interactive factors. It is concluded that the thermodynamical spontaneity of the IC adsorption parameters are greatly influenced by the interactive factors and not by the temperature changes alone.

  17. Preparation and characterization of platinum (Pt) and palladium (Pd) nanoparticle decorated graphene sheets and their utilization for the elimination of basic fuchsin and indigo carmine dyes

    NASA Astrophysics Data System (ADS)

    Kurt, Belma Zengin; Durmus, Zehra; Durmus, Ali

    2016-01-01

    In this study, graphene nano sheets, prepared with chemical oxidation and reduction routes via modified-Hummer method, were successfully decorated with platinum (Pt) and palladium (Pd) nanoparticles. Structural and morphological features of resulted graphene-metal nanocomposites were characterized with FT-IR, XRD, SEM and TEM methods. Anti-oxidant activity (AOA) values of nanocomposites were determined. The IC50 values of Pt-graphene and Pd-graphene nanocomposites were found to be 46.1 and 90.2 μg/mL, respectively based on the ABTS method and 80.2 and 143.7 μg/mL according to the DPPH method. It was found that the graphene-metal nanocomposites exhibited superior free radical scavenging activity compared to several types of noble metal nano particles although the nanocomposites consist of much lower amount of active metal sites than the nano-crystalline metal powders. It was consequently reported that the graphene-metal nanocomposites could be successfully used for the photocatalytic elimination of fuchsin and indigo carmine dyes under light irradiation.

  18. Stability of γ-Irradiated Carmine

    NASA Astrophysics Data System (ADS)

    Cosentino, Hélio M.; Fontenele, Rinaldo S.; DelMastro, Nélida L.

    2005-01-01

    Carmine is a dye used mainly for coloring food products and galenicals but also in inks. As food irradiation is becoming a regular treatment for food preservation, it is desirable to have a proper knowledge about the radiation sensitivity of additives that can be included in the food formula. The aim of this work was to establish the radiation stability of carmine against Co-60 gamma radiation. Samples of 50% pure carmine powder as well as 50%, 10% and 5% aqueous solutions were irradiated in a Gammacell 220, dose rate of about 5.2 kGy/h, with doses of 0, 1, 2, 4, 8, 16 and 32 kGy. Spectrophotometric readings at 494 nm show a slight decrease of the absorbance as a function of dose: Samples irradiated with 4 and 32 kGy retained 95% and 90% of absorbance of the unirradiated samples respectively. These results indicate a rather good stability of carmine against γ-irradiation.

  19. Solvent-free fluidic organic dye lasers.

    PubMed

    Choi, Eun Young; Mager, Loic; Cham, Tran Thi; Dorkenoo, Kokou D; Fort, Alain; Wu, Jeong Weon; Barsella, Alberto; Ribierre, Jean-Charles

    2013-05-01

    We report on the demonstration of liquid organic dye lasers based on 9-(2-ethylhexyl)carbazole (EHCz), so-called liquid carbazole, doped with green- and red-emitting laser dyes. Both waveguide and Fabry-Perot type microcavity fluidic organic dye lasers were prepared by capillary action under solvent-free conditions. Cascade Förster-type energy transfer processes from liquid carbazole to laser dyes were employed to achieve color-variable amplified spontaneous emission and lasing. Overall, this study provides the first step towards the development of solvent-free fluidic organic semiconducting lasers and demonstrates a new kind of optoelectronic applications for liquid organic semiconductors.

  20. Occupational asthma and food allergy due to carmine.

    PubMed

    Acero, S; Tabar, A I; Alvarez, M J; Garcia, B E; Olaguibel, J M; Moneo, I

    1998-09-01

    Carmine (E120), a natural red dye extracted from the dried females of the insect Dactylopius coccus var. Costa (cochineal), has been reported to cause hypersensitivity reactions. We report a case of occupational asthma and food allergy due to carmine in a worker not engaged in dye manufacturing. A 35-year-old nonatopic man, who had worked for 4 years in a spice warehouse, reported asthma and rhinoconjunctivitis for 5 months, related to carmine handling in his work. Two weeks before the visit, he reported one similar episode after the ingestion of a red-colored sweet containing carmine. Peak flow showed drops higher than 25% related to carmine exposure. Prick tests with the cochineal insect and carmine were positive, but negative to common aeroallergens, several mites, foods, and spices. The methacholine test was positive. Specific bronchial challenge test with a cochineal extract was positive with a dual pattern (20% and 24% fall in FEV1). Double-blind oral challenge with E120 was positive. The patient's sera contained specific IgE for various high-molecular-weight proteins from the cochineal extract, as shown by immunoblotting. Carmine proteins can induce IgE-mediated food allergy and occupational asthma in workers using products where its presence could be easily overlooked, as well as in dye manufacture workers. PMID:9788693

  1. Revised procedures for the certification of carmine (C.I. 75470, Natural red 4) as a biological stain.

    PubMed

    Dapson, R W; Frank, M; Penney, D P; Kiernan, J A

    2007-02-01

    Carmine is one of the original dyes certified by the Biological Stain Commission (BSC). Until now it has lacked both an assay procedure for dye content and a means to positively identify the dye. The methods for testing carmine in the laboratory of the BSC have been revised to include spectrophotometric examination at pH 12.5-12.6 to determine that the dye is carmine (lambda(max)=530-335 nm). The maximum absorbance of a solution containing 100 mg of dye per liter of water, adjusted to pH 12.5-12.6, which provides a relative measure of dye content, should lie in the range 1.2 to 1.8. If the dye is not carmine, spectrophotometry at pH 1.9-2.1 shows whether it is carminic acid (lambda(max)=490-500 nm) or 4-aminocarminic acid (lambda(max)=525-530 nm). The latter two dyes, which are also called carmine when sold as food colorants, have physical properties different from those of true carmine. The functional tests for carmine as a biological stain are Orth's lithium-carmine method for nuclei, Southgate's mucicarmine method for mucus, and Best's carmine method for glycogen. PMID:17510809

  2. Simultaneous determination of carminic acid, riboflavine, curcumin and erythrosine by derivative spectrophotometry and ratio spectra derivative.

    PubMed

    Nevado, J J; Cabanillas, C G; Salcedo, A M

    1994-05-01

    A quaternary mixture of carminic acid, riboflavine, curcumin and erythrosine can be resolved with a previous extraction step into metyl-isobutyl ketone and, resolving the binary mixtures obtained in the aqueous phase and organic phase, using derivative spectrophotometry on the basis of the zero-crossing measurements in the first derivative spectra as well as the first derivative of ratio spectra. The conditions of extraction established and the proposed methods have been tested to determine these colorants in several synthetic mixtures of four dyes, obtaining good recoveries. The methods have been applied in yoghurt samples spiked with the dyes. PMID:18966000

  3. Allergic contact dermatitis from carmine.

    PubMed

    Shaw, Daniel W

    2009-01-01

    A 28-year-old woman developed allergic contact dermatitis within 6 to 24 hours exclusively after using carmine-containing eyeshadows and lipsticks. She had both a positive patch test result and a positive antecubital repeated open application test result with carmine 2.5% in petrolatum. Thirty other patients had negative patch test results. Carmine is a widely used pigment derived from gravid cochineal insects. Carminic acid is the source of its color. Only two previous publications describing allergic contact dermatitis from carmine could be found. The ingredient in carmine causing these delayed hypersensitivity reactions has not been studied. In contrast, there are numerous reports of immediate hypersensitivity reactions from carmine, mostly from its use in foods and beverages but also from cosmetics and pharmaceuticals. These are immunoglobulin E-mediated reactions directed against cochineal proteins. PMID:19808007

  4. Allergic contact dermatitis from carmine.

    PubMed

    Shaw, Daniel W

    2009-01-01

    A 28-year-old woman developed allergic contact dermatitis within 6 to 24 hours exclusively after using carmine-containing eyeshadows and lipsticks. She had both a positive patch test result and a positive antecubital repeated open application test result with carmine 2.5% in petrolatum. Thirty other patients had negative patch test results. Carmine is a widely used pigment derived from gravid cochineal insects. Carminic acid is the source of its color. Only two previous publications describing allergic contact dermatitis from carmine could be found. The ingredient in carmine causing these delayed hypersensitivity reactions has not been studied. In contrast, there are numerous reports of immediate hypersensitivity reactions from carmine, mostly from its use in foods and beverages but also from cosmetics and pharmaceuticals. These are immunoglobulin E-mediated reactions directed against cochineal proteins.

  5. Continuous-wave organic dye lasers and methods

    SciTech Connect

    Shapira, Ofer; Chua, Song-Liang; Zhen, Bo; Lee, Jeongwon; Soljacic, Marin

    2014-09-16

    An organic dye laser produces a continuous-wave (cw) output without any moving parts (e.g., without using flowing dye streams or spinning discs of solid-state dye media to prevent photobleaching) and with a pump beam that is stationary with respect to the organic dye medium. The laser's resonant cavity, organic dye medium, and pump beam are configured to excite a lasing transition over a time scale longer than the associated decay lifetimes in the organic dye medium without photobleaching the organic dye medium. Because the organic dye medium does not photobleach when operating in this manner, it may be pumped continuously so as to emit a cw output beam. In some examples, operation in this manner lowers the lasing threshold (e.g., to only a few Watts per square centimeter), thereby facilitating electrical pumping for cw operation.

  6. On the early development of organic dyes for dye-sensitized solar cells.

    PubMed

    Kloo, Lars

    2013-07-28

    This viewpoint describes the background of the development of organic dyes for dye-sensitized solar cells, the impact of the 2006 ChemComm paper by Sun, Hagfeldt and co-workers regarding the D5 D-π-A-family of dyes, some recent developments and possible future challenges to meet.

  7. Decolorization of indigo carmine by laccase displayed on Bacillus subtilis spores.

    PubMed

    Cho, Eun-Ah; Seo, Jiyoung; Lee, Dong-Woo; Pan, Jae-Gu

    2011-06-10

    Blue multicopper oxidases, laccases displayed on the surface of Bacillus spores were used to decolorize a widely used textile dyestuff, indigo carmine. The laccase-encoding gene of Bacillus subtilis, cotA, was cloned and expressed in B. subtilis DB104, and the expressed enzyme was spontaneously localized on Bacillus spores. B. subtilis spores expressing laccase exhibited maximal activity for the oxidation of 2,2'-azino-bis (3-ethylthiazoline-6-sulfonate) (ABTS) at pH 4.0 and 80°C, and for the decolorization of indigo carmine at pH 8.0 and 60°C. The displayed enzyme retained 80% of its original activity after pre-treatment with organic solvents such as 50% acetonitrile and n-hexane for 2h at 37°C. The apparent K(m) of the enzyme displayed on spores was 443±124 μM for ABTS with a V(max) of 150 ± 16 U/mg spores. Notably, 1mg of spores displaying B. subtilis laccase (3.4 × 10(2)U for ABTS as a substrate) decolorized 44.6 μg indigo carmine in 2h. The spore reactor (0.5 g of spores corresponding to 1.7×10(5)U in 50 mL) in a consecutive batch recycling mode decolorized 223 mg indigo carmine/L to completion within 42 h at pH 8.0 and 60°C. These results suggest that laccase displayed on B. subtilis spores can serve as a powerful environmental tool for the treatment of textile dye effluent.

  8. Indigo Carmine for the Selective Endoscopic Intervertebral Nuclectomy

    PubMed Central

    Kim, Inn-Se; Shin, Sang-Wook; Kim, Tae-Kyun; Kim, Jeung-Il

    2005-01-01

    This study was undertaken to prove that the selectively infiltrated parts of nucleus pulposus with indigo carmine was degenerated parts of nucleus pulposus. This study was done, between August and October 2002, in 5 patients, who received endoscopic discectomy, due to intervertebral disc herniation. Discogram was done with mixture of indigo carmine and radioactive dye. Blue discolored part was removed through endoscope, and small undiscolored part was removed together for the control. The two parts were stained with hematoxylin and eosin and compared under the microscope. Undiscolored part was normal nucleus pulposus, composed of chondrocytes with a matrix of type II collagen and proteoglycan, mainly aggrecan. However, in discolored part, slits with destruction of collagen fiber array and ingrowth of vessel and nerve were observed. Using indigo carmine in endoscopic discectomy gives us selective removal of degenerated disc. PMID:16100472

  9. Molecular design and photovoltaic performance of organic dyes containing phenothiazine for dye-sensitized solar cells.

    PubMed

    Jo, Hyo Jeong; Nam, Jung Eun; Sim, Kyoseung; Kim, Dae-Hwan; Kim, Jae Hong; Kang, Jin-Kyu

    2014-10-01

    We synthesized novel organic photosensitizers based on fluorine-substituted phenothiazine with thiophene bridge units in the chromophore for application in dye-sensitized solar cells (DSSCs). Furthermore, organic dyes with different acceptors exhibited higher molar extinction coefficients, and better light absorption at longer wavelengths. The photovoltaic properties of organic dyes composed of different acceptors in their chromophores were measured to identify their effects on the DSSC performance. The organic dye, PFSCN2 containing multi-cyanoacrylic acid as the electron acceptor, showed a power conversion efficiency of 4.67% under AM 1.5 illumination (100 mW/cm2). The retarded recombination kinetics from TiO2 electrode to electrolyte enhanced the electron life time of the organic dye, PFSCN2 in the photoanode of the DSSC. This was confirmed with impedance analysis.

  10. Fundamental study on magnetic separation of organic dyes in wastewater

    NASA Astrophysics Data System (ADS)

    Fang, M.; Mishima, F.; Akiyama, Y.; Nishijima, S.

    2010-11-01

    The objective of this study is to separate dyes in wastewater with high efficiency and speed using High Gradient Magnetic Separation with superconducting magnet. Two main technologies are necessary for magnetic separation; one is magnetic seeding technology to provide ferromagnetism to the substance, and the other is magnetic separation technology using superconducting magnet and magnetic filters. In order to separate organic dyes, it is necessary to clarify the mechanism of magnetic seeding, and to design a suitable magnetic seeding method depending on the kind of object dye. Six kinds of dyes which are widely used in industry were adopted to investigate the possibility of the magnetic seeding and interaction mechanism between dye and ferromagnetic particles. As a result, it was shown that electrostatic interaction is one of the main interactions between organic dye and ferromagnetic particles.

  11. 21 CFR 73.2087 - Carmine.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2087 Carmine. (a) Identity and specifications. The color...)(2). (b) Use and restrictions. Carmine may be safely used in cosmetics generally, including cosmetics... provisions of § 70.25 of this chapter. (2) Cosmetics containing carmine that are not subject to...

  12. 21 CFR 73.2087 - Carmine.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2087 Carmine. (a) Identity and specifications. The color...)(2). (b) Use and restrictions. Carmine may be safely used in cosmetics generally, including cosmetics... provisions of § 70.25 of this chapter. (2) Cosmetics containing carmine that are not subject to...

  13. 21 CFR 73.2087 - Carmine.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2087 Carmine. (a) Identity and specifications. The color...)(2). (b) Use and restrictions. Carmine may be safely used in cosmetics generally, including cosmetics... chapter. (2) Cosmetics containing carmine that are not subject to the requirements of § 701.3 of...

  14. 21 CFR 73.2087 - Carmine.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2087 Carmine. (a) Identity and specifications. The color...)(2). (b) Use and restrictions. Carmine may be safely used in cosmetics generally, including cosmetics... provisions of § 70.25 of this chapter. (2) Cosmetics containing carmine that are not subject to...

  15. 21 CFR 73.2087 - Carmine.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2087 Carmine. (a) Identity and specifications. The color...)(2). (b) Use and restrictions. Carmine may be safely used in cosmetics generally, including cosmetics... provisions of § 70.25 of this chapter. (2) Cosmetics containing carmine that are not subject to...

  16. Structure of acid-stable carmine.

    PubMed

    Sugimoto, Naoki; Kawasaki, Yoko; Sato, Kyoko; Aoki, Hiromitsu; Ichi, Takahito; Koda, Takatoshi; Yamazaki, Takeshi; Maitani, Tamio

    2002-02-01

    Acid-stable carmine has recently been distributed in the U.S. market because of its good acid stability, but it is not permitted in Japan. We analyzed and determined the structure of the major pigment in acid-stable carmine, in order to establish an analytical method for it. Carminic acid was transformed into a different type of pigment, named acid-stable carmine, through amination when heated in ammonia solution. The features of the structure were clarified using a model compound, purpurin, in which the orientation of hydroxyl groups on the A ring of the anthraquinone skeleton is the same as that of carminic acid. By spectroscopic means and the synthesis of acid-stable carmine and purpurin derivatives, the structure of the major pigment in acid-stable carmine was established as 4-aminocarminic acid, a novel compound. PMID:11998314

  17. Spectrophotometric determination of vanadium in metallurgical products with carminic acid and cetyltrimethylammonium chloride

    SciTech Connect

    Babenko, N.L.; Blokh, M. Sh.; Guseva, T.D.

    1985-11-01

    According to the authors, there is an increasing demand for sensitive, selective, and rapid methods of determining low levels of vanadium in metallurgical products, and solvent-extraction methods do not meet the requirements. The authors used an anthraquinone dye carminic acid (CA) as a chromophoric organic reagent: 1, 3, 4, 6-tetrahydroxy-2-R-5carboxy-8-methylanthra-9, 10-quinone. The CSA was cetyltrimethylammonium chloride CTA. The three-component system was examined in order to devise a reasonably sensitive and rapid method of determining vanadium in metallurgical products. A study is made of the complexing in the system formed by vanadium (IV) with CA and the CSA. The optimum conditions for the formation of the complex have been established together with the spectrophotometric characteristics. A spectrophotometric method has been devised for determining from 0.05 to 5% of vanadium in metallurgical products with a relative standard deviation of not more than 0.04.

  18. Geometrical and energetical structural changes in organic dyes for dye-sensitized solar cells probed using photoelectron spectroscopy and DFT.

    PubMed

    Eriksson, Susanna K; Josefsson, Ida; Ellis, Hanna; Amat, Anna; Pastore, Mariachiara; Oscarsson, Johan; Lindblad, Rebecka; Eriksson, Anna I K; Johansson, Erik M J; Boschloo, Gerrit; Hagfeldt, Anders; Fantacci, Simona; Odelius, Michael; Rensmo, Håkan

    2016-01-01

    The effects of alkoxy chain length in triarylamine based donor-acceptor organic dyes are investigated with respect to the electronic and molecular surface structures on the performance of solar cells and the electron lifetime. The dyes were investigated when adsorbed on TiO2 in a configuration that can be used for dye-sensitized solar cells (DSCs). Specifically, the two dyes D35 and D45 were compared using photoelectron spectroscopy (PES) and density functional theory (DFT) calculations. The differences in solar cell characteristics when longer alkoxy chains are introduced in the dye donor unit are attributed to geometrical changes in dye packing while only minor differences were observed in the electronic structure. A higher dye load was observed for D45 on TiO2. However, D35 based solar cells result in higher photocurrent although the dye load is lower. This is explained by different geometrical structures of the dyes on the surface.

  19. [Absolute quantification of carminic acid in cochineal extract by quantitative NMR].

    PubMed

    Sugimoto, Naoki; Tada, Atsuko; Suematsu, Takako; Arifuku, Kazunori; Saito, Takeshi; Ihara, Toshihide; Yoshida, Yuuichi; Kubota, Reiji; Tahara, Maiko; Shimizu, Kumiko; Ito, Sumio; Yamazaki, Takeshi; Kawamura, Yoko; Nishimura, Tetsuji

    2010-01-01

    A quantitative NMR (qNMR) method was applied for the determination of carminic acid. Carminic acid is the main component in cochineal dye that is widely used as a natural food colorant. Since several manufacturers only provide reagent-grade carminic acid, there is no reference material of established purity. To improve the reliability of analytical data, we are developing quantitative nuclear magnetic resonance (qNMR), based on the fact that the intensity of a given NMR resonance is directly proportional to the molar amount of that nucleus in the sample. The purities and contents of carminic acid were calculated from the ratio of the signal intensities of an aromatic proton on carminic acid to nine protons of three methyl groups on DSS-d6 used as the internal standard. The concentration of DSS-d6 itself was corrected using potassium hydrogen phthalate, which is a certified reference material (CRM). The purities of the reagents and the contents of carminic acid in cochineal dye products were determined with SI-traceability as 25.3-92.9% and 4.6-30.5% based on the crystalline formula, carminic acid potassium salt trihydrate, which has been confirmed by X-ray analysis. The qNMR method does not require a reference compound, and is rapid and simple, with an overall analysis time of only 10 min. Our approach thus represents an absolute quantitation method with SI-traceability that should be readily applicable to analysis and quality control of any natural product. PMID:20208405

  20. Nitro group as a new anchoring group for organic dyes in dye-sensitized solar cells.

    PubMed

    Cong, Jiayan; Yang, Xichuan; Liu, Jing; Zhao, Jinxia; Hao, Yan; Wang, Yu; Sun, Licheng

    2012-07-01

    An organic dye JY1 bearing a nitro group was designed, synthesized and applied in DSCs. An unusual colour change was observed when the voltage applied to the device was reversed which was accompanied by a five-fold increase in the cell efficiency. We propose that applying a bias enabled the attachment of nitro groups to the TiO(2) surface.

  1. Structure-performance correlations of organic dyes with an electron-deficient diphenylquinoxaline moiety for dye-sensitized solar cells.

    PubMed

    Li, Sie-Rong; Lee, Chuan-Pei; Yang, Po-Fan; Liao, Chia-Wei; Lee, Mandy M; Su, Wei-Lin; Li, Chun-Ting; Lin, Hao-Wu; Ho, Kuo-Chuan; Sun, Shih-Sheng

    2014-08-01

    The high performances of dye-sensitized solar cells (DSSCs) based on seven new dyes are disclosed. Herein, the synthesis and electrochemical and photophysical properties of a series of intentionally designed dipolar organic dyes and their application in DSSCs are reported. The molecular structures of the seven organic dyes are composed of a triphenylamine group as an electron donor, a cyanoacrylic acid as an electron acceptor, and an electron-deficient diphenylquinoxaline moiety integrated in the π-conjugated spacer between the electron donor and acceptor moieties. The DSSCs based on the dye DJ104 gave the best overall cell performance of 8.06 %; the efficiency of the DSSC based on the standard N719 dye under the same experimental conditions was 8.82 %. The spectral coverage of incident photon-to-electron conversion efficiencies extends to the onset at the near-infrared region due to strong internal charge-transfer transition as well as the effect of electron-deficient diphenylquinoxaline to lower the energy gap in these organic dyes. A combined tetraphenyl segment as a hydrophobic barrier in these organic dyes effectively slows down the charge recombination from TiO2 to the electrolyte and boosts the photovoltage, comparable to their Ru(II) counterparts. Detailed spectroscopic studies have revealed the dye structure-cell performance correlations, to allow future design of efficient light-harvesting organic dyes.

  2. Screening π-conjugated bridges of organic dyes for dye-sensitized solar cells with panchromatic visible light harvesting

    NASA Astrophysics Data System (ADS)

    Yang, Zhenqing; Liu, Chunmeng; Shao, Changjin; Zeng, Xiaofei; Cao, Dapeng

    2016-07-01

    Developing highly efficient organic dyes with panchromatic visible light harvesting for dye-sensitized solar cells (DSSCs) is still one of the most important scientific challenges. Here, we design a series of phenothiazine derivative organic dyes with donor-π-acceptor (D-π-A) structure using density functional theory (DFT) and time-dependent DFT (TDDFT) based on experimentally synthesized typical SH-6 organic dyes. Results indicate that the newly designed BUCT13 - BUCT30 dyes show smaller HOMO-LUMO energy gaps, higher molar extinction coefficients and obvious redshifts compared to the SH-6 dye, and the maximum absorption peaks of eight dyes are greater than 650 nm among the newly designed dyes. In particular, BUCT27 exhibits a 234 nm redshift and the maximum molar extinction coefficient with an increment of about 80% compared to the SH-6 dye. BUCT19 exhibits not only a 269 nm redshift and higher molar extinction coefficient with an increment of about 50% compared to the SH-6 dye, but the extremely broad absorption spectrum covering the entire visible range up to the near-IR region of 1200 nm. It is expected that this work can provide a new strategy and guidance for the investigation of these dye-sensitized devices.

  3. Screening π-conjugated bridges of organic dyes for dye-sensitized solar cells with panchromatic visible light harvesting.

    PubMed

    Yang, Zhenqing; Liu, Chunmeng; Shao, Changjin; Zeng, Xiaofei; Cao, Dapeng

    2016-07-01

    Developing highly efficient organic dyes with panchromatic visible light harvesting for dye-sensitized solar cells (DSSCs) is still one of the most important scientific challenges. Here, we design a series of phenothiazine derivative organic dyes with donor-π-acceptor (D-π-A) structure using density functional theory (DFT) and time-dependent DFT (TDDFT) based on experimentally synthesized typical SH-6 organic dyes. Results indicate that the newly designed BUCT13 - BUCT30 dyes show smaller HOMO-LUMO energy gaps, higher molar extinction coefficients and obvious redshifts compared to the SH-6 dye, and the maximum absorption peaks of eight dyes are greater than 650 nm among the newly designed dyes. In particular, BUCT27 exhibits a 234 nm redshift and the maximum molar extinction coefficient with an increment of about 80% compared to the SH-6 dye. BUCT19 exhibits not only a 269 nm redshift and higher molar extinction coefficient with an increment of about 50% compared to the SH-6 dye, but the extremely broad absorption spectrum covering the entire visible range up to the near-IR region of 1200 nm. It is expected that this work can provide a new strategy and guidance for the investigation of these dye-sensitized devices. PMID:27188528

  4. Screening π-conjugated bridges of organic dyes for dye-sensitized solar cells with panchromatic visible light harvesting.

    PubMed

    Yang, Zhenqing; Liu, Chunmeng; Shao, Changjin; Zeng, Xiaofei; Cao, Dapeng

    2016-07-01

    Developing highly efficient organic dyes with panchromatic visible light harvesting for dye-sensitized solar cells (DSSCs) is still one of the most important scientific challenges. Here, we design a series of phenothiazine derivative organic dyes with donor-π-acceptor (D-π-A) structure using density functional theory (DFT) and time-dependent DFT (TDDFT) based on experimentally synthesized typical SH-6 organic dyes. Results indicate that the newly designed BUCT13 - BUCT30 dyes show smaller HOMO-LUMO energy gaps, higher molar extinction coefficients and obvious redshifts compared to the SH-6 dye, and the maximum absorption peaks of eight dyes are greater than 650 nm among the newly designed dyes. In particular, BUCT27 exhibits a 234 nm redshift and the maximum molar extinction coefficient with an increment of about 80% compared to the SH-6 dye. BUCT19 exhibits not only a 269 nm redshift and higher molar extinction coefficient with an increment of about 50% compared to the SH-6 dye, but the extremely broad absorption spectrum covering the entire visible range up to the near-IR region of 1200 nm. It is expected that this work can provide a new strategy and guidance for the investigation of these dye-sensitized devices.

  5. The degradation of organic dyes by corona discharge

    SciTech Connect

    Goheen, S.C.; McCulloch, M.; Durham, D.E.; Heath, W.O.

    1992-02-01

    Several dyes in water were individually exposed to corona discharge. Light absorbance decreased for all organic dyes with time. Absorbance losses with methylene blue, malachite green, and new coccine were studied. The loss of color was followed using an in situ colorimeter and the effects of varying the current, voltage, gas phase, stirring rates, salinity, and electrode spacing were investigated. The highest reaction rates were observed using the highest current, highest voltage (up to 10kV), highest stirring rate, lowest salinity, smallest electrode spacing, and an environment containing enhanced levels of oxygen. Current was higher in the presence of nitrogen than in the presence of oxygen (for the same voltage), but the reaction of methylene blue did not proceed unless oxygen was present. These results help identify conditions using corona discharge in which dyes, and potentially other organics, can be destroyed. 22 refs., 5 figs.

  6. Organic Semiconductors based on Dyes and Color Pigments.

    PubMed

    Gsänger, Marcel; Bialas, David; Huang, Lizhen; Stolte, Matthias; Würthner, Frank

    2016-05-01

    Organic dyes and pigments constitute a large class of industrial products. The utilization of these compounds in the field of organic electronics is reviewed with particular emphasis on organic field-effect transistors. It is shown that for most major classes of industrial dyes and pigments, i.e., phthalocyanines, perylene and naphthalene diimides, diketopyrrolopyrroles, indigos and isoindigos, squaraines, and merocyanines, charge-carrier mobilities exceeding 1 cm(2) V(-1) s(-1) have been achieved. The most widely investigated molecules due to their n-channel operation are perylene and naphthalene diimides, for which even values close to 10 cm(2) V(-1) s(-1) have been demonstrated. The fact that all of these π-conjugated colorants contain polar substituents leading to strongly quadrupolar or even dipolar molecules suggests that indeed a much larger structural space shows promise for the design of organic semiconductor molecules than was considered in this field traditionally. In particular, because many of these dye and pigment chromophores demonstrate excellent thermal and (photo-)chemical stability in their original applications in dyeing and printing, and are accessible by straightforward synthetic protocols, they bear a particularly high potential for commercial applications in the area of organic electronics.

  7. Organic Semiconductors based on Dyes and Color Pigments.

    PubMed

    Gsänger, Marcel; Bialas, David; Huang, Lizhen; Stolte, Matthias; Würthner, Frank

    2016-05-01

    Organic dyes and pigments constitute a large class of industrial products. The utilization of these compounds in the field of organic electronics is reviewed with particular emphasis on organic field-effect transistors. It is shown that for most major classes of industrial dyes and pigments, i.e., phthalocyanines, perylene and naphthalene diimides, diketopyrrolopyrroles, indigos and isoindigos, squaraines, and merocyanines, charge-carrier mobilities exceeding 1 cm(2) V(-1) s(-1) have been achieved. The most widely investigated molecules due to their n-channel operation are perylene and naphthalene diimides, for which even values close to 10 cm(2) V(-1) s(-1) have been demonstrated. The fact that all of these π-conjugated colorants contain polar substituents leading to strongly quadrupolar or even dipolar molecules suggests that indeed a much larger structural space shows promise for the design of organic semiconductor molecules than was considered in this field traditionally. In particular, because many of these dye and pigment chromophores demonstrate excellent thermal and (photo-)chemical stability in their original applications in dyeing and printing, and are accessible by straightforward synthetic protocols, they bear a particularly high potential for commercial applications in the area of organic electronics. PMID:27028553

  8. Enzyme immunoassay for carminic acid in foods.

    PubMed

    Yoshida, A; Takagaki, Y; Nishimune, T

    1995-01-01

    A competitive enzyme immunoassay (EIA) for carminic acid was investigated. Monoclonal anticarminic acid antibody was obtained from A/J mice immunized with carminic acid-human immunoglobulin G (IgG) conjugate. Carminic acid was extracted with distilled water from beverage, jelly, candy, pasta sauce, yogurt, or ice cream samples. Ham or fish paste samples were digested with pronase, then carminic acid was extracted from samples with sodium hydroxide solution. The extract was diluted more than 10-fold with 1% gelatin in borate buffer solution. Microtiter plates were coated with carminic acid-bovine serum albumin (BSA) conjugate or just BSA. Goat anti-mouse IgG(H+L)-peroxidase complex was used as a second antibody, and 3,3',5,5'-tetramethylbenzidine was used as a substrate for the peroxidase. The working range for quantitative analysis was 0.3-10 ng/mL, and the detection limit was 0.2 micrograms/g original sample. Recoveries of carminic acid by this assay were > 95% for milk beverage and jelly, and > 85% for yogurt and fish paste. Carminic acid was detected in 7 of 26 red-colored commercial food products and ranged from 3.5 to 356 micrograms/g. This EIA system also responded to the structural analogue of carminic acid, laccaic acid. PMID:7756895

  9. Photoproducts of carminic acid formed by a composite from Manihot dulcis waste.

    PubMed

    Antonio-Cisneros, Cynthia M; Dávila-Jiménez, Martín M; Elizalde-González, María P; García-Díaz, Esmeralda

    2015-04-15

    Carbon-TiO2 composites were obtained from carbonised Manihot dulcis waste and TiO2 using glycerol as an additive and thermally treating the composites at 800 °C. Furthermore, carbon was obtained from manihot to study the adsorption, desorption and photocatalysis of carminic acid on these materials. Carminic acid, a natural dye extracted from cochineal insects, is a pollutant produced by the food industry and handicrafts. Its photocatalysis was observed under different atmospheres, and kinetic curves were measured by both UV-Vis and HPLC for comparison, yielding interesting differences. The composite was capable of decomposing approximately 50% of the carminic acid under various conditions. The reaction was monitored by UV-Vis spectroscopy and LC-ESI-(Qq)-TOF-MS-DAD, enabling the identification of some intermediate species. The deleterious compound anthracene-9,10-dione was detected both in N2 and air atmospheres. PMID:25466082

  10. Organic synthetic dye degradation by modified pinhole discharge

    NASA Astrophysics Data System (ADS)

    Lončarić Božić, A.; Koprivanac, N.; Šunka, P.; Člupek, M.; Babický, V.

    2004-03-01

    The aim of this work was to investigate the possibility of applying a high voltage pulsed electrical discharges for dye wastewater treatment. Commercial organic monochlorotriazine reactive dye of the anthraquinone type C.I. Reactive Blue 49 (RB49) was chosen as a representative of persistent and recalcitrant wastewater pollutant. The modified pinhole discharge flow-through reactor was used to treat such type of contaminant. Applying HV pulses 30 kV, 3.15 J/pulse, 50 Hz repetition rate, complete decolorisation and partial mineralization of RB49 has been reached and demonstrated by means of UV/VIS absorption, TOC and AOX measurements.

  11. Organic dyes removal using magnetically modified rye straw

    NASA Astrophysics Data System (ADS)

    Baldikova, Eva; Safarikova, Mirka; Safarik, Ivo

    2015-04-01

    Rye straw, a very low-cost material, was employed as a biosorbent for two organic water-soluble dyes belonging to different dye classes, namely acridine orange (acridine group) and methyl green (triarylmethane group). The adsorption properties were tested for native and citric acid-NaOH modified rye straw, both in nonmagnetic and magnetic versions. The adsorption equilibrium was reached in 2 h and the adsorption isotherms data were analyzed using the Langmuir model. The highest values of maximum adsorption capacities were 208.3 mg/g for acridine orange and 384.6 mg/g for methyl green.

  12. Organics Verification Study for Sinclair and Dyes Inlets, Washington

    SciTech Connect

    Kohn, Nancy P.; Brandenberger, Jill M.; Niewolny, Laurie A.; Johnston, Robert K.

    2006-09-28

    Sinclair and Dyes Inlets near Bremerton, Washington, are on the State of Washington 1998 303(d) list of impaired waters because of fecal coliform contamination in marine water, metals in sediment and fish tissue, and organics in sediment and fish tissue. Because significant cleanup and source control activities have been conducted in the inlets since the data supporting the 1998 303(d) listings were collected, two verification studies were performed to address the 303(d) segments that were listed for metal and organic contaminants in marine sediment. The Metals Verification Study (MVS) was conducted in 2003; the final report, Metals Verification Study for Sinclair and Dyes Inlets, Washington, was published in March 2004 (Kohn et al. 2004). This report describes the Organics Verification Study that was conducted in 2005. The study approach was similar to the MVS in that many surface sediment samples were screened for the major classes of organic contaminants, and then the screening results and other available data were used to select a subset of samples for quantitative chemical analysis. Because the MVS was designed to obtain representative data on concentrations of contaminants in surface sediment throughout Sinclair Inlet, Dyes Inlet, Port Orchard Passage, and Rich Passage, aliquots of the 160 MVS sediment samples were used in the analysis for the Organics Verification Study. However, unlike metals screening methods, organics screening methods are not specific to individual organic compounds, and are not available for some target organics. Therefore, only the quantitative analytical results were used in the organics verification evaluation. The results of the Organics Verification Study showed that sediment quality outside of Sinclair Inlet is unlikely to be impaired because of organic contaminants. Similar to the results for metals, in Sinclair Inlet, the distribution of residual organic contaminants is generally limited to nearshore areas already within the

  13. Removal of dyes using immobilized titanium dioxide illuminated by fluorescent lamps.

    PubMed

    Zainal, Zulkarnain; Hui, Lee Kong; Hussein, Mohd Zobir; Taufiq-Yap, Yun Hin; Abdullah, Abdul Halim; Ramli, Irmawati

    2005-10-17

    The photodegradation of various dyes in aqueous solution was studied. Experiments were carried out using glass coated titanium dioxide thin film as photocatalyst. Photodegradation processes of methylene blue (MB), methyl orange (MO), indigo carmine (IC), chicago sky blue 6B (CSB), and mixed dye (MD, mixture of the four mentioned single dye) were reported. As each photodegradation system is pH dependent, the photodegradation experiment was carried out in each dye photodegradation reactive pH range at approximately 28 degrees C. The dyes removal efficiency was studied and compared using UV-vis spectrophotometer analysis. The total removal of each dye was: methylene blue (90.3%), methyl orange (98.5%), indigo carmine (92.4%), chicago sky blue 6B (60.3%), and mixed dyes (70.1%), respectively. The characteristic of the photocatalyst was investigated using X-ray diffractometer (XRD). The amount of each dye intermediate produced in the photodegradation process was also determined with the help of total organic carbon (TOC) analysis.

  14. Visible Light-Induced Carbonylation Reactions with Organic Dyes as the Photosensitizers.

    PubMed

    Peng, Jin-Bao; Qi, Xinxin; Wu, Xiao-Feng

    2016-09-01

    Dyes can CO do it: Organic dyes and pigments are usually applied in textile dyeing, which can be dated back to the Neolithic period. Interestingly, the possibility to use organic dyes as photoredox catalysts has also been noticed by organic chemists and applied in organic synthesis. Carbonylation reactions as a powerful procedure in carbonyl-containing compound preparation have also been studied. In this manuscript, the recent achievements in using organic dyes as visible-light sensitizers in carbonylation chemistry are summarized and discussed.

  15. Visible Light-Induced Carbonylation Reactions with Organic Dyes as the Photosensitizers.

    PubMed

    Peng, Jin-Bao; Qi, Xinxin; Wu, Xiao-Feng

    2016-09-01

    Dyes can CO do it: Organic dyes and pigments are usually applied in textile dyeing, which can be dated back to the Neolithic period. Interestingly, the possibility to use organic dyes as photoredox catalysts has also been noticed by organic chemists and applied in organic synthesis. Carbonylation reactions as a powerful procedure in carbonyl-containing compound preparation have also been studied. In this manuscript, the recent achievements in using organic dyes as visible-light sensitizers in carbonylation chemistry are summarized and discussed. PMID:27488198

  16. Ultra-high-performance liquid chromatography/tandem high-resolution mass spectrometry analysis of sixteen red beverages containing carminic acid: identification of degradation products by using principal component analysis/discriminant analysis.

    PubMed

    Gosetti, Fabio; Chiuminatto, Ugo; Mazzucco, Eleonora; Mastroianni, Rita; Marengo, Emilio

    2015-01-15

    The study investigates the sunlight photodegradation process of carminic acid, a natural red colourant used in beverages. For this purpose, both carminic acid aqueous standard solutions and sixteen different commercial beverages, ten containing carminic acid and six containing E120 dye, were subjected to photoirradiation. The results show different patterns of degradation, not only between the standard solutions and the beverages, but also from beverage to beverage. Due to the different beverage recipes, unpredictable reactions take place between the dye and the other ingredients. To identify the dye degradation products in a very complex scenario, a methodology was used, based on the combined use of principal component analysis with discriminant analysis and ultra-high-performance liquid chromatography coupled with tandem high resolution mass spectrometry. The methodology is unaffected by beverage composition and allows the degradation products of carminic acid dye to be identified for each beverage. PMID:25149011

  17. Ultra-high-performance liquid chromatography/tandem high-resolution mass spectrometry analysis of sixteen red beverages containing carminic acid: identification of degradation products by using principal component analysis/discriminant analysis.

    PubMed

    Gosetti, Fabio; Chiuminatto, Ugo; Mazzucco, Eleonora; Mastroianni, Rita; Marengo, Emilio

    2015-01-15

    The study investigates the sunlight photodegradation process of carminic acid, a natural red colourant used in beverages. For this purpose, both carminic acid aqueous standard solutions and sixteen different commercial beverages, ten containing carminic acid and six containing E120 dye, were subjected to photoirradiation. The results show different patterns of degradation, not only between the standard solutions and the beverages, but also from beverage to beverage. Due to the different beverage recipes, unpredictable reactions take place between the dye and the other ingredients. To identify the dye degradation products in a very complex scenario, a methodology was used, based on the combined use of principal component analysis with discriminant analysis and ultra-high-performance liquid chromatography coupled with tandem high resolution mass spectrometry. The methodology is unaffected by beverage composition and allows the degradation products of carminic acid dye to be identified for each beverage.

  18. Salicylic Acid-Based Organic Dyes Acting as the Photosensitizer for Solar Cells.

    PubMed

    Hong, Sungjun; Park, Jae-Hyeong; Han, Ah-Reum; Ko, Kwan-Woo; Eom, Jin Hee; Namgoong, Sung Keon; Lo, Alvie S V; Gordon, Keith C; Yoon, Sungho; Han, Chi-Hwan

    2016-05-01

    A D-π-A metal-free organic dye, featuring salicylic acid as a novel acceptor/anchoring unit, has been designed, synthesized and applied to dye-sensitized solar cell. The detailed photophysical, electrochemical, photovoltaic and sensitizing properties of the organic dye were investigated, in addition to the computational studies of the dye and dye-(TiO2)6 system. A solar cell device using this new organic dye as a sensitizer produced a solar to electric power conversion efficiency (PCE) of 3.49% (J(sc) = 6.69 mAcm-2, V(oc) = 0.74 V and ff = 0.70) under 100 mWcm(-2) simulated AM 1.5 G solar irradiation, demonstrating that the salicylic acid-based organic dye is a suitable alternative to currently used organometallic dyes.

  19. Salicylic Acid-Based Organic Dyes Acting as the Photosensitizer for Solar Cells.

    PubMed

    Hong, Sungjun; Park, Jae-Hyeong; Han, Ah-Reum; Ko, Kwan-Woo; Eom, Jin Hee; Namgoong, Sung Keon; Lo, Alvie S V; Gordon, Keith C; Yoon, Sungho; Han, Chi-Hwan

    2016-05-01

    A D-π-A metal-free organic dye, featuring salicylic acid as a novel acceptor/anchoring unit, has been designed, synthesized and applied to dye-sensitized solar cell. The detailed photophysical, electrochemical, photovoltaic and sensitizing properties of the organic dye were investigated, in addition to the computational studies of the dye and dye-(TiO2)6 system. A solar cell device using this new organic dye as a sensitizer produced a solar to electric power conversion efficiency (PCE) of 3.49% (J(sc) = 6.69 mAcm-2, V(oc) = 0.74 V and ff = 0.70) under 100 mWcm(-2) simulated AM 1.5 G solar irradiation, demonstrating that the salicylic acid-based organic dye is a suitable alternative to currently used organometallic dyes. PMID:27483839

  20. DCM-based organic dyes with electron donating groups for dye-sensitized solar cells.

    PubMed

    Kim, Joo Young; Yoon, Seung Soo; Kim, Young Sik

    2014-07-01

    Herein, 4-(dicyanomethylene)-2-methyl-6-[p-(dimethylamino)styryl]-4H-pyran (DCM)-based dyes with electron donating groups were designed and their electronic and optical properties were investigated theoretically for dye-sensitized solar cells (DSSCs). Among the dyes, the D1 and D2 dyes were composed of single electron donating group and the D3 and D4 dyes composed of dual donating group. We performed DFT/TDDFT calculations to get insight into the factors responsible for photovoltaic properties as dye sensitizers. It showed that all the dyes in this work are available as dye sensitizers from the energy consideration compared to TiO2 electrode and iodide electrolyte. It also showed that the D3 and D4 dyes produced additional absorption bands by the introduction of dual donor in absorption spectra and the absorption band of the D4 dye is more red-shifted than that of the D3 dye. It is attributed to the fact that the M2 (a coumarin derivative) moiety with stronger electron withdrawing ability stabilized its LUMO level. In terms of molar extinction coefficient and panchromatic feature, we suggest that the D4 dye would show better performance than other dyes in the present study as a dye sensitizer for DSSCs.

  1. First principles study of organic sensitizers for dye sensitized solar cells: effects of anchoring groups on optoelectronic properties and dye aggregation.

    PubMed

    Nachimuthu, Santhanamoorthi; Chen, Wei-Chieh; Leggesse, Ermias Girma; Jiang, Jyh-Chiang

    2016-01-14

    We have designed a new set of D-π-A type organic dye sensitizers with different acceptor and anchoring groups, and systematically investigated their optoelectronic properties for efficient dye sensitized solar cell applications. Particularly, we have focused on the effects of anchoring groups on the dye aggregation phenomenon. TDDFT results indicate that the dyes with CSSH anchoring groups exhibit improved optoelectronic properties compared to other dyes. Further, molecular dynamics simulations have been performed to describe the formation of dye aggregation due to intermolecular hydrogen bonding. The observed results indicate that dyes with CSSH anchoring groups are less prone to aggregate because of their very weak intermolecular interactions.

  2. Severe Hypotension, Hypoxia, and Subcutaneous Erythema Induced by Indigo Carmine Administration during Open Prostatectomy

    PubMed Central

    Voelzke, Bryan B.

    2016-01-01

    Indigo carmine (also known as 5,5′-indigodisulfonic acid sodium salt or indigotine) is a blue dye that is administered intravenously to examine the urinary tract and usually is biologically safe and inert. Indigo carmine rarely may cause adverse reactions. We treated a 66-year-old man who had general anesthesia and radical retropubic prostatectomy for prostate cancer. He had a previous history of allergy to bee sting with nausea, vomiting, and dizziness. Within 1 minute after injection of indigo carmine for evaluation of the ureters, the patient developed hypotension to 40 mmHg, severe hypoxia (the value of SpO2 (peripheral capillary oxygen saturation) was 75% on 40% inspired oxygen concentration), poor air movement and bilateral diffuse wheezing on auscultation, and marked subcutaneous erythema at the upper extremities. After treatment with 100% oxygen, epinephrine (total, 1.5 mg), hydrocortisone (100 mg), diphenhydramine (50 mg), albuterol nebulizer (0.083%), and continuous infusion of epinephrine (0.15 μg/kg/min), the vital signs became stable, and he recovered completely. In summary, indigo carmine rarely may cause life-threatening anaphylactic or anaphylactoid reaction that may necessitate rapid treatment to stabilize cardiovascular, hemodynamic, and pulmonary function.

  3. Severe Hypotension, Hypoxia, and Subcutaneous Erythema Induced by Indigo Carmine Administration during Open Prostatectomy

    PubMed Central

    Voelzke, Bryan B.

    2016-01-01

    Indigo carmine (also known as 5,5′-indigodisulfonic acid sodium salt or indigotine) is a blue dye that is administered intravenously to examine the urinary tract and usually is biologically safe and inert. Indigo carmine rarely may cause adverse reactions. We treated a 66-year-old man who had general anesthesia and radical retropubic prostatectomy for prostate cancer. He had a previous history of allergy to bee sting with nausea, vomiting, and dizziness. Within 1 minute after injection of indigo carmine for evaluation of the ureters, the patient developed hypotension to 40 mmHg, severe hypoxia (the value of SpO2 (peripheral capillary oxygen saturation) was 75% on 40% inspired oxygen concentration), poor air movement and bilateral diffuse wheezing on auscultation, and marked subcutaneous erythema at the upper extremities. After treatment with 100% oxygen, epinephrine (total, 1.5 mg), hydrocortisone (100 mg), diphenhydramine (50 mg), albuterol nebulizer (0.083%), and continuous infusion of epinephrine (0.15 μg/kg/min), the vital signs became stable, and he recovered completely. In summary, indigo carmine rarely may cause life-threatening anaphylactic or anaphylactoid reaction that may necessitate rapid treatment to stabilize cardiovascular, hemodynamic, and pulmonary function. PMID:27610263

  4. Severe Hypotension, Hypoxia, and Subcutaneous Erythema Induced by Indigo Carmine Administration during Open Prostatectomy.

    PubMed

    Nandate, Koichiro; Voelzke, Bryan B

    2016-01-01

    Indigo carmine (also known as 5,5'-indigodisulfonic acid sodium salt or indigotine) is a blue dye that is administered intravenously to examine the urinary tract and usually is biologically safe and inert. Indigo carmine rarely may cause adverse reactions. We treated a 66-year-old man who had general anesthesia and radical retropubic prostatectomy for prostate cancer. He had a previous history of allergy to bee sting with nausea, vomiting, and dizziness. Within 1 minute after injection of indigo carmine for evaluation of the ureters, the patient developed hypotension to 40 mmHg, severe hypoxia (the value of SpO2 (peripheral capillary oxygen saturation) was 75% on 40% inspired oxygen concentration), poor air movement and bilateral diffuse wheezing on auscultation, and marked subcutaneous erythema at the upper extremities. After treatment with 100% oxygen, epinephrine (total, 1.5 mg), hydrocortisone (100 mg), diphenhydramine (50 mg), albuterol nebulizer (0.083%), and continuous infusion of epinephrine (0.15 μg/kg/min), the vital signs became stable, and he recovered completely. In summary, indigo carmine rarely may cause life-threatening anaphylactic or anaphylactoid reaction that may necessitate rapid treatment to stabilize cardiovascular, hemodynamic, and pulmonary function. PMID:27610263

  5. 494 Skin Sensitization to Carmine Before Onset of Systemic Allergy to Ingested Carmine

    PubMed Central

    Katada, Yoshinori; Harada, Yoshinori; Azuma, Naoto; Hashimoto, Jun; Saeki, Yukihiko; Tanaka, Toshio

    2012-01-01

    Background Allergic sensitization to food can occur through skin exposure. We investigated anaphylactic cases due to carmine, a food additive extracted from Dactylopius coccus. Methods Screening all patients, who visited our department from January 2000 to December 2009, we identified 2 new such cases. Both had history of rash induced by certain cosmetics containig carmine. We further investigated previous case reports of carmine allergy, whether skin sensitization antedated food allergy or not. Results Case 1: A 26-year-old woman visited our hospital because of anaphylaxis occurred within 5 minutes after ingesting a Japanese YOKAN (sweetened and jellied bean paste). IgE antibodies against common food allergens including beans and wheat were all negative. As the paste contains carmine, we tested specific IgE antibody, which was positive. She had been avoiding using certain cheeks and lips for 2 years, since they cause erythema. These cosmetics emerged as containing carmine. Abstaining from the food additive made her free from anaphylaxis. Case 2: A 30-year-old woman came to our hospital for dyspnea, uriticaria, and bilateral blepharedema, immediately after drinking Campari soda. Her past history was prominent, as she had 4 episodes of anaphylaxis in 4 years, requiring emergency transport twice. All anaphylactic episodes occurred in Italian restaurants when she drank cocktails, which might contain carmine in Campari soda. She had been also sensitive to certain rouges since several years before the first onset of anaphylaxis. It became clear that the rouges contained carmine. In literatures, we found 22 cases with allergy to ingested carmine. It is surprising that all cases were women (aged 25 to 52), while occupationally sensitized patients are predominantly men. As far as we could know, 85.7 % of (6/7) mentioned cases had previous history of sensitization to cosmetics containing carmine. Conclusions In many cases with allergy against ingested carmine, the route of

  6. Metal-free organic dyes for TiO2 and ZnO dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Selopal, Gurpreet Singh; Wu, Hui-Ping; Lu, Jianfeng; Chang, Yu-Cheng; Wang, Mingkui; Vomiero, Alberto; Concina, Isabella; Diau, Eric Wei-Guang

    2016-01-01

    We report the synthesis and characterization of new metal-free organic dyes (namely B18, BTD-R, and CPTD-R) which designed with D-π-A concept to extending the light absorption region by strong conjugation group of π-linker part and applied as light harvester in dye sensitized solar cells (DSSCs). We compared the photovoltaic performance of these dyes in two different photoanodes: a standard TiO2 mesoporous photoanode and a ZnO photoanode composed of hierarchically assembled nanostructures. The results demonstrated that B18 dye has better photovoltaic properties compared to other two dyes (BTD-R and CPTD-R) and each dye has higher current density (Jsc) when applied to hierarchical ZnO nanocrystallites than the standard TiO2 mesoporous film. Transient photocurrent and photovoltage decay measurements (TCD/TVD) were applied to systematically study the charge transport and recombination kinetics in these devices, showing the electron life time (τR) of B18 dye in ZnO and TiO2 based DSSCs is higher than CPTD-R and BTD-R based DSSCs, which is consistent with the photovoltaic performances. The conversion efficiency in ZnO based DSSCs can be further boosted by 35%, when a compact ZnO blocking layer (BL) is applied to inhibit electron back reaction.

  7. Metal-free organic dyes for TiO2 and ZnO dye-sensitized solar cells

    PubMed Central

    Selopal, Gurpreet Singh; Wu, Hui-Ping; Lu, Jianfeng; Chang, Yu-Cheng; Wang, Mingkui; Vomiero, Alberto; Concina, Isabella; Diau, Eric Wei-Guang

    2016-01-01

    We report the synthesis and characterization of new metal-free organic dyes (namely B18, BTD-R, and CPTD-R) which designed with D-π-A concept to extending the light absorption region by strong conjugation group of π-linker part and applied as light harvester in dye sensitized solar cells (DSSCs). We compared the photovoltaic performance of these dyes in two different photoanodes: a standard TiO2 mesoporous photoanode and a ZnO photoanode composed of hierarchically assembled nanostructures. The results demonstrated that B18 dye has better photovoltaic properties compared to other two dyes (BTD-R and CPTD-R) and each dye has higher current density (Jsc) when applied to hierarchical ZnO nanocrystallites than the standard TiO2 mesoporous film. Transient photocurrent and photovoltage decay measurements (TCD/TVD) were applied to systematically study the charge transport and recombination kinetics in these devices, showing the electron life time (τR) of B18 dye in ZnO and TiO2 based DSSCs is higher than CPTD-R and BTD-R based DSSCs, which is consistent with the photovoltaic performances. The conversion efficiency in ZnO based DSSCs can be further boosted by 35%, when a compact ZnO blocking layer (BL) is applied to inhibit electron back reaction. PMID:26738698

  8. Interaction of protonated merocyanine dyes with amines in organic solvents

    NASA Astrophysics Data System (ADS)

    Ribeiro, Eduardo Alberton; Sidooski, Thiago; Nandi, Leandro Guarezi; Machado, Vanderlei Gageiro

    2011-10-01

    2,6-Diphenyl-4-(2,4,6-triphenylpyridinium-1-yl)phenolate ( 1a) and 4-[(1-methyl-4(1 H)-pyridinylidene)-ethylidene]-2,5-cyclohexadien-1-one ( 2a) were protonated in organic solvents (dichloromethane, acetonitrile, and DMSO) to form 1b and 2b, respectively. The appearance of the solvatochromic bands of 1a and 2a was studied UV-vis spectrophotometrically by deprotonation of 1b and 2b in solution in the presence of the following amines: aniline (AN), N-methylaniline (NMAN), N, N-dimethylaniline (NDAN), n-butylamine (BA), diethylamine (DEA), and triethylamine (TEA). Titrations of 1b and 2b with the amines were carried out and the binding constants were determined from the titration curves in each solvent, using a mathematical model adapted from the literature which considers the simultaneous participation of two dye: amine stoichiometries, 1:1 and 1:2. The data obtained showed the following base order for the two compounds in DMSO: BA > DEA > TEA, while aromatic amines did not cause any effect. In dichloromethane, the following base order for 1b was verified: TEA > DEA > BA ≫NDAN, while for 2b the order was: TEA > DEA > BA, suggesting that 1b is more acidic than 2b. The data in acetonitrile indicated for 1b and 2b the following order for the amines: DEA > TEA > BA. The diversity of the experimental data were explained based on a model that considers the level of interaction of the protonated dyes with the amines to be dependent on three aspects: (a) the basicity of the amine, which varies according to their molecular structure and the solvent in which it is dissolved, (b) the molecular structure of the dye, and (c) the solvent used to study the system.

  9. Insights into aggregation effects on optical property and electronic coupling of organic dyes in dye sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Feng, Shuai; Li, Quan-Song; Yang, Li-Na; Sun, Zhu-Zhu; Niehaus, Thomas A.; Li, Ze-Sheng

    2015-01-01

    Combining density functional theory (DFT), time-dependent DFT, and density functional tight binding (DFTB) methods, we present a computational investigation on the aggregation effects of two organic dyes, WS-2 and WS-6, which are used as sensitizers in dye sensitized solar cells (DSSCs). The calculated absorption and emission spectra in solution and on TiO2 agree well with the experimental observations, which demonstrate WS-6 is less prone to aggregation due to a hexyl substituent on the thiophene ring compared to WS-2. Importantly, our results predict strong aggregation interactions inducing larger electronic coupling between the stacking dimers, which may be detrimental for electronic injection from dye to TiO2 and partly responsible for the loss of photo-voltaic efficiency. The deeper understanding of the dye aggregation effects shed lights on a better knowledge about the complex factors determining the function of DSSC and rational design of high efficiency sensitizers.

  10. Catalytic degradation of organic dyes using biosynthesized silver nanoparticles.

    PubMed

    Vidhu, V K; Philip, Daizy

    2014-01-01

    The green synthesis of metallic nanoparticles paved the way to improve and protect the environment by decreasing the use of toxic chemicals and eliminating biological risks in biomedical applications. Plant mediated synthesis of metal nanoparticles is gaining more importance owing to its simplicity, rapid rate of synthesis of nanoparticles and eco-friendliness. The present article reports an environmentally benign and unexploited method for the synthesis of silver nanocatalysts using Trigonella foenum-graecum seeds, which is a potential source of phytochemicals. The UV-visible absorption spectra of the silver samples exhibited distinct band centered around 400-440 nm. The major phytochemicals present in the seed extract responsible for the formation of silver nanocatalysts are identified using FTIR spectroscopy. The report emphasizes the effect of the size of silver nanoparticles on the degradation rate of hazardous dyes, methyl orange, methylene blue and eosin Y by NaBH4. The efficiency of silver nanoparticles as a promising candidate for the catalysis of organic dyes by NaBH4 through the electron transfer process is established in the present study.

  11. Deposition of organic dyes for dye-sensitized solar cell by using matrix-assisted pulsed laser evaporation

    NASA Astrophysics Data System (ADS)

    Yen, Chih-Ping; Yu, Pin-Feng; Wang, Jyhpyng; Lin, Jiunn-Yuan; Chen, Yen-Mu; Chen, Szu-yuan

    2016-08-01

    The deposition of various distinct organic dyes, including ruthenium complex N3, melanin nanoparticle (MNP), and porphyrin-based donor-π-acceptor dye YD2-o-C8, by using matrix-assisted pulsed laser evaporation (MAPLE) for application to dye-sensitized solar cell (DSSC) is investigated systematically. It is found that the two covalently-bonded organic molecules, i.e., MNP and YD2-o-C8, can be transferred from the frozen target to the substrate with maintained molecular integrity. In contrast, N3 disintegrates in the process, presumably due to the lower bonding strength of metal complex compared to covalent bond. With the method, DSSC using YD2-o-C8 is fabricated, and an energy conversion efficiency of 1.47% is attained. The issue of the low penetration depth of dyes deposited by MAPLE and the possible resolution to it are studied. This work demonstrates that MAPLE could be an alternative way for deposition of organic dyes for DSSC.

  12. Case study on the destruction of organic dyes in supercritical water

    SciTech Connect

    LaJeunesse, C.A.; Rice, S.F.

    1994-11-01

    Organic dyes, which were used in Navy shells to mark ships and structures, need to be disposed of without burning. A study was undertaken to assess the feasibility of using supercritical water oxidation to destroy organic dyes. Experimental destruction efficiencies, product analyses, and process configuration are reported.

  13. Decolorization and biodegradation of Indigo carmine by a textile soil isolate Paenibacillus larvae.

    PubMed

    Ramya, Mohandass; Anusha, Bhaskar; Kalavathy, S

    2008-04-01

    The potential of recently isolated bacteria Paenibacillus larvae for the effective decolorization of Indigo carmine was evaluated. The effects of operational parameters (temperature, pH, dye concentration, shaking/non shaking) were tested. Maximum extent of decolorization was observed when the medium was incorporated with 10 g/l of yeast extract and peptone. Decolorization was strongly inhibited at non-shaken conditions as well as incorporation of inorganic sources (sodium nitrite and ammonium chloride) in the medium. Maximum decolorization was observed at 30 degrees C (100%) and 40 degrees C (92%) at 8 h of incubation. The LC-MS and NMR analysis confirms the oxidation of Indigo carmine . The primary degradation products were found to be Isatin sulfonic acid and anthranilicacid.

  14. Selective adsorption and separation of organic dyes from aqueous solution on polydopamine microspheres.

    PubMed

    Fu, Jianwei; Xin, Qianqian; Wu, Xuechen; Chen, Zhonghui; Yan, Ya; Liu, Shujun; Wang, Minghuan; Xu, Qun

    2016-01-01

    Polydopamine (PDA) microspheres, synthesized by a facile oxidation polymerization route, were evaluated as a potential adsorbent for selective adsorption and separation of organic dyes. The adsorption processes towards nine water-soluble dyes (anionic dyes: methyl orange (MO), eosin-Y (EY), eosin-B (EB), acid chrome blue K (ACBK), neutral dye: neutral red (NR), and cationic dyes: rhodamine B (RhB), malachite green (MG), methylene blue (MB), safranine T (ST)) were thoroughly investigated. The adsorption selectivity of organic dyes onto PDA microspheres was successfully applied for the separation of dyes mixtures. Various influential factors such as solution pH, temperature, and contact time were employed to ascertain the optimal condition for adsorption of representative organic dyes including MB, MG and NR. The pseudo-first-order and pseudo-second-order kinetics models were used to fit the adsorption kinetics process. Five isothermal adsorption models (Langmuir, Dubnin-Radushkevich, Temkin, Freundlich and Harkins-Jura) were used to investigate the adsorption thermodynamics properties. The results showed that the PDA microspheres owned good selective adsorption ability towards cationic dyes. The adsorption kinetics process conformed to the pseudo-second-order kinetics model and the Langmuir isotherm model was more appropriate for tracing the adsorption behavior than other isotherm models. Thus, we can conclude PDA microspheres may be a high-efficiency selective adsorbent towards some cationic dyes.

  15. Selective adsorption and separation of organic dyes from aqueous solution on polydopamine microspheres.

    PubMed

    Fu, Jianwei; Xin, Qianqian; Wu, Xuechen; Chen, Zhonghui; Yan, Ya; Liu, Shujun; Wang, Minghuan; Xu, Qun

    2016-01-01

    Polydopamine (PDA) microspheres, synthesized by a facile oxidation polymerization route, were evaluated as a potential adsorbent for selective adsorption and separation of organic dyes. The adsorption processes towards nine water-soluble dyes (anionic dyes: methyl orange (MO), eosin-Y (EY), eosin-B (EB), acid chrome blue K (ACBK), neutral dye: neutral red (NR), and cationic dyes: rhodamine B (RhB), malachite green (MG), methylene blue (MB), safranine T (ST)) were thoroughly investigated. The adsorption selectivity of organic dyes onto PDA microspheres was successfully applied for the separation of dyes mixtures. Various influential factors such as solution pH, temperature, and contact time were employed to ascertain the optimal condition for adsorption of representative organic dyes including MB, MG and NR. The pseudo-first-order and pseudo-second-order kinetics models were used to fit the adsorption kinetics process. Five isothermal adsorption models (Langmuir, Dubnin-Radushkevich, Temkin, Freundlich and Harkins-Jura) were used to investigate the adsorption thermodynamics properties. The results showed that the PDA microspheres owned good selective adsorption ability towards cationic dyes. The adsorption kinetics process conformed to the pseudo-second-order kinetics model and the Langmuir isotherm model was more appropriate for tracing the adsorption behavior than other isotherm models. Thus, we can conclude PDA microspheres may be a high-efficiency selective adsorbent towards some cationic dyes. PMID:26407057

  16. Nano- and microparticles of organic fluorescent dyes: self-organization and optical properties.

    PubMed

    Fery-Forgues, Suzanne; Abyan, Mouhammad; Lamere, Jean-François

    2008-01-01

    Organic nanostructured materials are of increasing interest for applications in the fields of bioanalysis, photocatalysis, photonics, and organic light-emitting diodes. However, their preparation is still difficult to control and their optical properties are inadequately known. A solvent-exchange process called the "reprecipitation method" was used here to prepare nano- and microcrystals from fluorescent dyes belonging, for example, to the coumarin and nitrobenzoxadiazole (NBD) series. Typically, the dyes were dissolved in a hydrophilic organic solvent and then suddenly placed in an aqueous environment, where they spontaneously produce molecular assemblies. According to the self-association properties of the dyes and to the experimental conditions used, the nano- and microcrystals obtained exhibited different sizes and shapes, as observed by fluorescence and electron microscopy. In some cases, the crystal habit was controlled by adding some additives to the reprecipitation medium. The overall optical properties of the free-standing particles in suspension were generally quite close to those of the dissolved dyes. However, strong distortions of the absorption and emission spectra were observed for crystals grown in the presence of ionic additives. Under the fluorescence microscope, individual microcrystals may show peculiar emission characteristics, displaying bright and dark zones, or behaving like tiny optical fibers.

  17. Advanced organic dye for high-speed, high-density optical media

    NASA Astrophysics Data System (ADS)

    Kodaira, Takuo; Matsuda, Isao; Somei, Hidenori; Tsuzuki, Takeo; Yokoyama, Daizo; Endo, Akihisa; Takeguchi, Kazunobu; Kojo, Shinichi; Miyazawa, Fuyuki; Otsu, Takeshi; Murai, Wakaaki; Hattori, Masashi; Shimomai, Kenichi; Oshita, Junji; Asano, Sho; Shimizu, Atsuo; Fujii, Toru

    2015-09-01

    Advances in organic dye progress are indispensable for high-speed, high-density recording of recordable Blu-ray Disc™ (BD-R) low-to-high (LTH) discs without a low elastic modulus layer. The optimal physical properties of the organic dyes, i.e., a low decomposition calorific value, a low decomposition temperature, and a large n-value, were determined, and a dye with these properties was synthesized. A BD-R disc using the dye conformed to the BD-R LTH standard at 8× recording and ever higher speeds should be possible. Furthermore, the possibility of 33 GB/layer high-density recording was suggested.

  18. Composite nanofibers for highly efficient photocatalytic degradation of organic dyes from contaminated water.

    PubMed

    Mohamed, Alaa; El-Sayed, Ramy; Osman, T A; Toprak, M S; Muhammed, M; Uheida, A

    2016-02-01

    In this study highly efficient photocatalyst based on composite nanofibers containing polyacrylonitrile (PAN), carbon nanotubes (CNT), and surface functionalized TiO2 nanoparticles was developed. The composite nanofibers were fabricated using electrospinning technique followed by chemical crosslinking. The surface modification and morphology changes of the fabricated composite nanofibers were examined through SEM, TEM, and FTIR analysis. The photocatalytic performance of the composite nanofibers for the degradation of model molecules, methylene blue and indigo carmine, under UV irradiation in aqueous solutions was investigated. The results demonstrated that high photodegradation efficiency was obtained in a short time and at low power intensity compared to other reported studies. The effective factors on the degradation of the dyes, such as the amount of catalyst, solution pH and irradiation time were investigated. The experimental kinetic data were fitted using pseudo-first order model. The effect of the composite nanofibers as individual components on the degradation efficiency of MB and IC was evaluated in order to understand the overall photodegradation mechanism. The results obtained showed that all the components possess significant effect on the photodegradation activity of the composite nanofibers. The stability studies demonstrated that the photodegradation efficiency can remain constant at the level of 99% after five consecutive cycles. PMID:26615225

  19. Composite nanofibers for highly efficient photocatalytic degradation of organic dyes from contaminated water.

    PubMed

    Mohamed, Alaa; El-Sayed, Ramy; Osman, T A; Toprak, M S; Muhammed, M; Uheida, A

    2016-02-01

    In this study highly efficient photocatalyst based on composite nanofibers containing polyacrylonitrile (PAN), carbon nanotubes (CNT), and surface functionalized TiO2 nanoparticles was developed. The composite nanofibers were fabricated using electrospinning technique followed by chemical crosslinking. The surface modification and morphology changes of the fabricated composite nanofibers were examined through SEM, TEM, and FTIR analysis. The photocatalytic performance of the composite nanofibers for the degradation of model molecules, methylene blue and indigo carmine, under UV irradiation in aqueous solutions was investigated. The results demonstrated that high photodegradation efficiency was obtained in a short time and at low power intensity compared to other reported studies. The effective factors on the degradation of the dyes, such as the amount of catalyst, solution pH and irradiation time were investigated. The experimental kinetic data were fitted using pseudo-first order model. The effect of the composite nanofibers as individual components on the degradation efficiency of MB and IC was evaluated in order to understand the overall photodegradation mechanism. The results obtained showed that all the components possess significant effect on the photodegradation activity of the composite nanofibers. The stability studies demonstrated that the photodegradation efficiency can remain constant at the level of 99% after five consecutive cycles.

  20. A push-pull organic dye with a quinoidal thiophene linker: Photophysical properties and solvent effects

    NASA Astrophysics Data System (ADS)

    Climent, Clàudia; Carreras, Abel; Alemany, Pere; Casanova, David

    2016-10-01

    In the present work we perform a computational study of the properties of a push-pull organic dye with a quinoidal thiophene unit as the conjugated linker between the electron donor and acceptor groups. We investigate the photophysical properties of the dye related to its potential use as a molecular sensitizer in dye-sensitized solar cells. We rationalize the solvation effects on the absorption band of the dye in protic and aprotic solvents, identifying the interaction of alcohol solvents with the amine in the donor group as the source for the blue shift of the absorption band with respect to aprotic solvents.

  1. Preparation and spectral characterization of polymeric nanocapsules containing DR1 organic dye

    NASA Astrophysics Data System (ADS)

    Sharifimehr, Mohammad Reza; Ghanbari, Khadijeh; Ayoubi, Kazem; Mohajerani, Ezedin

    2015-07-01

    In order to provide necessary degree of freedom for organic dye molecules in optical applications and also for safety improvement, water insoluble Disperse Red 1 (DR1) dye molecules were placed inside the polymeric nanocapsules along with suitable surfactants and using controlled phase-separation method. TEM images were used to investigate the morphology of prepared nanocapsules. Total dye concentration for a solution consist of obtained polymeric nanocapsules was determined using decomposition of nanocapsules and a reference absorption spectrum. Absorption spectrum of a solution containing DR1 and dichloromethane was also compared with prepared nanocapsules at the same dye concentration, thereby a red-shift in absorption spectrum was detected.

  2. Wavelength-Tunable Microlasers Based on the Encapsulation of Organic Dye in Metal-Organic Frameworks.

    PubMed

    Wei, Yanhui; Dong, Haiyun; Wei, Cong; Zhang, Wei; Yan, Yongli; Zhao, Yong Sheng

    2016-09-01

    A wavelength-tunable microlaser is realized based on the controlled intramolecular charge transfer (ICT) process in dye-encapsulated metal-organic framework (MOF) material. The confinement effect of the MOFs is beneficial for low-threshold lasing. By effectively controlling the polarity of the MOF pores, the population distribution between the locally excited and ICT states is continuously modulated, thus achieving broadband tunable MOF-based microlasers. PMID:27314453

  3. Wavelength-Tunable Microlasers Based on the Encapsulation of Organic Dye in Metal-Organic Frameworks.

    PubMed

    Wei, Yanhui; Dong, Haiyun; Wei, Cong; Zhang, Wei; Yan, Yongli; Zhao, Yong Sheng

    2016-09-01

    A wavelength-tunable microlaser is realized based on the controlled intramolecular charge transfer (ICT) process in dye-encapsulated metal-organic framework (MOF) material. The confinement effect of the MOFs is beneficial for low-threshold lasing. By effectively controlling the polarity of the MOF pores, the population distribution between the locally excited and ICT states is continuously modulated, thus achieving broadband tunable MOF-based microlasers.

  4. [1]Benzothieno[3,2-b]benzothiophene-Based Organic Dyes for Dye-Sensitized Solar Cells.

    PubMed

    Capodilupo, Agostina L; Fabiano, Eduardo; De Marco, Luisa; Ciccarella, Giuseppe; Gigli, Giuseppe; Martinelli, Carmela; Cardone, Antonio

    2016-04-15

    Three new metal-free organic dyes with the [1]benzothieno[3,2-b]benzothiophene (BTBT) π-bridge, having the structure donor-π-acceptor (D-π-A) and labeled as 19, 20 and 21, have been designed and synthesized for application in dye-sensitized solar cells (DSSC). Once the design of the π-acceptor block was fixed, containing the BTBT as the π-bridge and the cyanoacrylic group as the electron acceptor and anchoring unit, we selected three donor units with different electron-donor capacity, in order to assemble new chromophores with high molar extinction coefficients (ε), whose absorption features well reflect the good performance of the final DSSC devices. Starting with the 19 dye, which shows a molar extinction coefficient ε of over 14,000 M(-1) cm(-1) and takes into account the absorption maximun at the longer wavelength, the substitution of the BFT donor unit with the BFA yields a great enhancement of absorptivity (molar extinction coefficient ε > 42,000 M(-1) cm(-1)), until reaching the higher value (ε > 69,000 M(-1) cm(-1)) with the BFPhz donor unit. The good general photovoltaic performances obtained with the three dyes highlight the suitable properties of electron-transport of the BTBT as the π-bridge in organic chromophore for DSSC, making this very cheap and easy to synthesize molecule particularly attractive for efficient and low-cost photovoltaic devices. PMID:26986652

  5. White light-emitting diode with quasisolar spectrum based on organic fluorescent dyes

    NASA Astrophysics Data System (ADS)

    Chung, Shuang-Chao; Li, Ming-Chia; Sun, Ching-Cherng

    2015-07-01

    We present a study of light-emitting diodes (LEDs) using organic fluorescent dyes to replace the general phosphor. The blue die with a specific organic fluorescent dye gives the LED a single color appearance. Through a color-mixing cavity, multiple LEDs are used to produce a quasisolar spectrum at a certain band and white light with a color rendering index as high as 97 at around 2800 K.

  6. Simultaneous determination of eleven dyes and their aluminum lakes in drugs.

    PubMed

    Ishikawa, Fusako; Shigeoka, Sutemi; Nagashima, Machiko; Takahashi, Misako; Kamimura, Hisashi

    2003-01-01

    A 3-step extraction method was developed for the simultaneous determination of 11 dyes and their aluminum lakes in drugs. The dyes were first extracted with warm water (approximately 60 degrees C) and were cleaned up by solid-phase extraction with a tC18 cartridge. Aluminum lake dyes that remained in the precipitate were extracted with 0.02M NaOH. Aluminum in the dye lakes was reextracted into the organic layer with acetylacetone-butyl acetate (1 + 9, v/v), as an acetylacetone chelate, and was quantified by atomic absorption spectrometry. The dye portions of the aluminum lakes remained in the aqueous layer and were cleaned up in the same way as the dyes. The dyes and the dye portions of the aluminum lakes were quantified by ion-pair liquid chromatography with a photodiode array detector within 20 min. The recoveries of dyes from drug fortified at 10 microg of each dye per pill were 87.0-102.2%, and the recoveries of dyes from drugs fortified at 50 microg of each dye lake per pill were 82.9-101.6%, except for recoveries of indigo carmine. In 40 ethical and over-the-counter drugs, dyes that were not indicated in the package insert information for drugs were detected in 5 samples. The highest amount of dye found in a drug was 1169.5 microg erythrosine, which was detected in a capsule of antibiotic. Aluminum lake dyes were detected in 8 samples of various dosage forms. PMID:12723908

  7. [Rapid Synthesis of Metal Organic Framework and Its Adsorption Properties on Anonic Dyes].

    PubMed

    Sun, De-shuai; Liu, Ya-li; Zhang, Xiao-dong; Qin, Ting-ting

    2016-03-15

    The waste water containing dyes is difficult to be biochemically treated because of its deep color. Adsorption becomes an important treatment method for this kind of waste water. The iron organic framework was rapidly synthesized at room temperature, and characterized by IR and XRD. Adsorption properties of the materials were tested using four anonic dyes solutions. It was found that the iron organic framework could be formed rapidly, with higher surface area and pore volumes. The pH value of zero point charge was 3.7. The adsorption experiments showed that the iron organic material could remove more dyes in acid solution. The dye adsorption capacity increased with increasing dye concentration. These adsorption data fitted well with Langmuir thermoadsorption equation. The calculated parameter from Langmuir adsorption indicated that the adsorption process could be performed easily. The second order kinetic equation could describe the adsorption data. In addition, the structure of dyes could affect the adsorption process. The metal complex dyes could be quickly removed. PMID:27337895

  8. [Rapid Synthesis of Metal Organic Framework and Its Adsorption Properties on Anonic Dyes].

    PubMed

    Sun, De-shuai; Liu, Ya-li; Zhang, Xiao-dong; Qin, Ting-ting

    2016-03-15

    The waste water containing dyes is difficult to be biochemically treated because of its deep color. Adsorption becomes an important treatment method for this kind of waste water. The iron organic framework was rapidly synthesized at room temperature, and characterized by IR and XRD. Adsorption properties of the materials were tested using four anonic dyes solutions. It was found that the iron organic framework could be formed rapidly, with higher surface area and pore volumes. The pH value of zero point charge was 3.7. The adsorption experiments showed that the iron organic material could remove more dyes in acid solution. The dye adsorption capacity increased with increasing dye concentration. These adsorption data fitted well with Langmuir thermoadsorption equation. The calculated parameter from Langmuir adsorption indicated that the adsorption process could be performed easily. The second order kinetic equation could describe the adsorption data. In addition, the structure of dyes could affect the adsorption process. The metal complex dyes could be quickly removed.

  9. 21 CFR 73.1100 - Cochineal extract; carmine.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1100 Cochineal extract; carmine. (a) Identity and specifications. (1) The color additives cochineal extract and carmine shall conform in identity and specifications to the requirements of § 73.100(a) (1) and (2) and (b). (2) Color...

  10. 21 CFR 73.1100 - Cochineal extract; carmine.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1100 Cochineal extract; carmine. (a) Identity and specifications. (1) The color additives cochineal extract and carmine shall conform in identity and specifications to the requirements of § 73.100(a) (1) and (2) and (b). (2) Color...

  11. 21 CFR 73.1100 - Cochineal extract; carmine.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1100 Cochineal extract; carmine. (a) Identity and specifications. (1) The color additives cochineal extract and carmine shall conform in identity and specifications to the requirements of § 73.100(a) (1) and (2) and (b). (2) Color...

  12. 21 CFR 73.1100 - Cochineal extract; carmine.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1100 Cochineal extract; carmine. (a) Identity and specifications. (1) The color additives cochineal extract and carmine shall conform in identity and specifications to the requirements of § 73.100(a) (1) and (2) and (b). (2) Color...

  13. Femtosecond spectroscopic study of carminic acid DNA interactions

    NASA Astrophysics Data System (ADS)

    Comanici, Radu; Gabel, Bianca; Gustavsson, Thomas; Markovitsi, Dimitra; Cornaggia, Christian; Pommeret, Stanislas; Rusu, Catalin; Kryschi, Carola

    2006-06-01

    Photo-excited carminic acid and carminic acid-DNA complexes in a buffer solution at pH 7 have been examined using a variety of spectroscopy techniques, that are in particular, the femtosecond resolved fluorescence upconversion and transient absorption spectroscopy. The observation of dual fluorescence emission, one peaks at 470 nm and the other at 570 nm, indicates to an excited-state (S 1) intramolecular proton transfer (ESIPT). A detailed analysis of the transient absorption measurements of an aqueous carminic-acid solution at pH 7 yielded four lifetimes for the excited-state (S 1): 8, 15, 33 and 46 ps. On the other hand, only two lifetimes, 34 and 47 ps, were observed by fluorescence upconversion spectroscopy because of the detection limitation to the long wavelength edge of the carminic-acid spectrum. The four S 1 lifetimes were ascribed to the coexistence of respectively two tautomer (normal and tautomer) forms of carminic acid, in the non-dissociated state (CAH) and in the deprotonated state (CA -). The fluorescence upconversion measurements of carminic acid-DNA complexes exhibited a prolongation of the fluorescence lifetimes. This effect was accepted as evidence for the formation of intercalation complexes between the carminic acid and the DNA. The intercalative binding of the carminic acid to DNA was confirmed by the fluorescence titration experiments resulting to a binding constant of 2 × 10 5 M -1 that is typical for anthracycline-DNA complexes.

  14. Influence of selected fluorescent dyes on small aquatic organisms

    NASA Astrophysics Data System (ADS)

    Rowiński, Paweł; Chrzanowski, Marcin

    2011-02-01

    Rhodamine B and Rhodamine WT are fluorescent dyes commonly used as tracers in hydrological investigations. Since introducing intensely red substances into rivers raises understandable doubts of ecological nature, the authors aimed at examining the influence of these dyes on small water fauna using bioindication methods. Quantitative results, calculated with the use of Bliss-Weber probit statistical method, were achieved by means of standardized ecotoxicological tests containing ready-to-hatch resting forms of fairy shrimp (Thamnocephalus platyurus). Qualitative studies included observation of water flea crustacean (Daphnia magna) and horned planorbis snail (Planorbis corneus), both typically present in rivers and representative for temperate climate, as well as guppy fish (Poecilla reticulata), paramecium protozoan (Paramaecium caudatum) and the above-mentioned fairy shrimp. The investigation revealed that both dyes in concentrations used for hydrological purposes are low enough to exert almost no toxic impact on water fauna considered.

  15. Novel D-A-π-A organic dyes based on 3-dimensional triarylamine and benzothiadiazole derivatives for high-performance dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Huang, Hongli; Chen, Huajie; Long, Jun; Wang, Guo; Tan, Songting

    2016-09-01

    Organic dyes with a 3-dimensional (3D) structure is helpful for retarding dyes aggregation and charge recombination as well as improving the power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). In this contribution, a novel 3D triarylamine derivative (IDTTPA) featuring an indenothiophenene unit has been designed, synthesized, and applied to develop a 3D organic dyes. Two novel D-A-π-A organic dyes (CD1 and CD2) based on IDTTPA as the electron donors, 2,1,3-benzothiadiazole derivatives as the auxiliary acceptors, and formic acid as the anchoring groups have been successfully synthesized and applied in DSSCs. The effects of the fluoro substitute groups on the photophysical, electrochemical, and photovoltaic properties are investigated. The results indicate that the fluoro-containing dye CD2 exhibits higher molar extinction coefficient, stronger light-capturing ability, and better photovoltaic performance than those of CD1 dye without fluoro substitute. Investigation of the DSSCs performance shows that CD2-based DSSCs exhibit a high PCE value of 7.91%, higher than that of CD1-based DSSCs (6.29%), even higher than that of the reference DSSCs based on N719 (7.49%). This works has demonstrated that this kind of 3D unit (IDTTPA) is a strong and promising electron donor unit to develop high efficiency metal-free organic dyes.

  16. Development and validation of a quantitative method for determination of carmine (E120) in foodstuffs by liquid chromatography: NMKL Collaborative Study.

    PubMed

    Merino, L; Edberg, U; Tidriks, H

    1997-01-01

    A liquid chromatographic method for quantitative determination of carmine (E120) in different foodstuffs is described. Qualitative and semiquantitative methods for analysis of carmine and other related dyes are well established. However, quantitative methods available are based mainly on enzymatic reactions that are time-consuming or specific for analysis of carminic acid in yoghurt. In the method developed and validated here, carminic acid is extracted by boiling the sample with HCl, purified on a solid-phase extraction cartridge, and injected on a C18 analytical column. The method was evaluated by an internal analytical quality control and a collaborative study in which 11 laboratories from the Nordic countries participated. The food samples analyzed were fruit jelly, liqueur, juice, yoghurt, and ice cream. Materials were distributed to participants as uniform level and split level. Validation showed that the proposed method is well suited for quantitative determination of carmine. The detection limit is 0.1 mg/L. The mean relative standard deviation for reproducibility varies from 7.9 to 11.7%. The proposed method is simple and relatively fast compared with previously published methods. PMID:9325582

  17. Hierarchical Organization of Organic Dyes and Protein Cages into Photoactive Crystals.

    PubMed

    Mikkilä, Joona; Anaya-Plaza, Eduardo; Liljeström, Ville; Caston, Jose R; Torres, Tomas; Escosura, Andrés de la; Kostiainen, Mauri A

    2016-01-26

    Phthalocyanines (Pc) are non-natural organic dyes with wide and deep impact in materials science, based on their intense absorption at the near-infrared (NIR), long-lived fluorescence and high singlet oxygen ((1)O2) quantum yields. However, Pcs tend to stack in buffer solutions, losing their ability to generate singlet oxygen, which limits their scope of application. Furthermore, Pcs are challenging to organize in crystalline structures. Protein cages, on the other hand, are very promising biological building blocks that can be used to organize different materials into crystalline nanostructures. Here, we combine both kinds of components into photoactive biohybrid crystals. Toward this end, a hierarchical organization process has been designed in which (a) a supramolecular complex is formed between octacationic zinc Pc (1) and a tetraanionic pyrene (2) derivatives, driven by electrostatic and π-π interactions, and (b) the resulting tetracationic complex acts as a molecular glue that binds to the outer surface anionic patches of the apoferritin (aFt) protein cage, inducing cocrystallization. The obtained ternary face-centered cubic (fcc) packed cocrystals, with diameters up to 100 μm, retain the optical properties of the pristine dye molecules, such as fluorescence at 695 nm and efficient light-induced (1)O2 production. Considering that (1)O2 is utilized in important technologies such as photodynamic therapy (PDT), water treatments, diagnostic arrays and as an oxidant in organic synthesis, our results demonstrate a powerful methodology to create functional biohybrid systems with unprecedented long-range order. This approach should greatly aid the development of nanotechnology and biomedicine.

  18. Effect of the co-sensitization sequence on the performance of dye-sensitized solar cells with porphyrin and organic dyes.

    PubMed

    Fan, Suhua; Lu, Xuefeng; Sun, Hong; Zhou, Gang; Chang, Yuan Jay; Wang, Zhong-Sheng

    2016-01-14

    To obtain a broad spectral response in the visible region, TiO2 film is co-sensitized with a porphyrin dye (FNE57 or FNE59) and an organic dye (FNE46). It is found that the stepwise co-sensitization in one single dye solution followed by in another single dye solution is better than the co-sensitization in a cocktail solution in terms of photovoltaic performance. The stepwise co-sensitization first with a porphyrin dye and then with an organic dye outperforms that in a reverse order. DSSC devices based on co-sensitizers FNE57 + FNE46 and FNE59 + FNE46 with a quasi-solid-state gel electrolyte generate power conversion efficiencies of 7.88% and 8.14%, respectively, which exhibits remarkable efficiency improvements of 61% and 35%, as compared with devices sensitized with the porphyrin dyes FNE57 and FNE59, respectively. Co-sensitization brings about a much improved short-circuit photocurrent due to the complementary absorption of the two sensitizers. The observed enhancement of incident monochromatic photon-to-electron conversion efficiency from individual dye sensitization to co-sensitization is attributed to the improved charge collection efficiency rather than to the light harvesting efficiency. Interestingly, the open-circuit photovoltage for the co-sensitization system comes between the higher voltage for the porphyrin dye (FNE57 or FNE59) and the lower voltage for the organic dye (FNE46), which is well correlated with their electron lifetimes. This finding indicates that not only the spectral complementation but also the electron lifetime should be considered to select dyes for co-sensitization. PMID:26651077

  19. Synthesis, linear optical, non-linear optical, thermal and mechanical characterizations of dye-doped semi-organic NLO crystals

    NASA Astrophysics Data System (ADS)

    Sesha Bamini, N.; Vidyalakshmy, Y.; Choedak, Tenzin; Kejalakshmy, N.; Muthukrishnan, P.; Ancy, C. J.

    2015-06-01

    Organic laser dyes Coumarin 485, Coumarin 540 and Rhodamine 590 Chloride were used to dope potassium acid phthalate crystals (KAP). Dye-doped KAP crystals with different dye concentrations such as 0.01 mM, 0.03 mM, 0.05 mM, 0.07 mM and 0.09 mM (in the KAP growth solution) were grown. The linear optical, non-linear optical, mechanical and thermal characterizations of dye-doped KAP crystals were studied and compared to understand the effect of dye and dye concentration on the KAP crystal. Absorption and emission studies of KAP and dye-doped KAP single crystals indicated the inclusion of the dye into the KAP crystal lattice. The effect of dye and its concentration on the SHG efficiency of the KAP crystal was studied using the Kurtz and Perry powder technique. It was observed that the absorption maximum wavelength and concentration of the dye used for doping the KAP single crystal decided the SHG efficiency of the dye-doped KAP single crystals. The mechanical hardness of the dye-doped and undoped (pure) KAP single crystals were studied using the Vickner’s microhardness test. It was observed that doping the KAP crystals with the laser dyes changed them from softer material to harder material. Etching studies showed an improvement in the optical quality of the KAP crystal after doping with laser dyes.

  20. Carminic acid-promoted oxygen radical damage to lipid and carbohydrate.

    PubMed

    Gutteridge, J M; Quinlan, G J

    1986-01-01

    The food colouring carminic acid redox cycles to produce free radicals. These radicals, in the presence of trace amounts of iron salts, readily damage membrane lipid and degrade the carbohydrate deoxyribose. Damage to membrane lipid appears to involve mainly organic oxygen radicals such as alkoxy and peroxy radicals, whereas that to deoxyribose implicates the hydroxyl radical formed in a Fenton-type reaction. Antioxidants and iron chelators prevent such damage. PMID:3803637

  1. TDDFT screening auxiliary withdrawing group and design the novel D-A-π-A organic dyes based on indoline dye for highly efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Yang, Zhenqing; Liu, Yun; Liu, Chunmeng; Lin, Chundan; Shao, Changjin

    2016-10-01

    Based on the experimentally synthesized dye JZ145, we designed a series of novel D-A-π-A dyes SPL201-SPL211 with different π-conjugated bridges and a new auxiliary withdrawing group for highly efficient dye-sensitized solar cells (DSSCs) using density functional theory (DFT) and time-dependent DFT(TDDFT). The molecular structures, energy levels, absorption spectra, light-harvesting efficiency (LHE), driving force of injection(ΔGinj) and regeneration(ΔGreg), electron dipole moment (μnormal) and lifetime of the first excited state(τ) were all scrutinized in details. Results reveal that the additional withdrawing group A2 and the π-conjugated group di-η-hexyl-substituted cyclopentadithiophene (CPDT) are more promising functional groups for the organic dyes with D-A-π-A structure. We further designed SPL212 and SPL213 by employing indoline group as donor, the above screened functional groups as π-conjugated bridge and additional withdrawing group, biscarbodithiolic acid and dicyanovinyl sulfonic acid groups as acceptor group. We found that SPL212 exhibits not only a higher molar extinction coefficient with an increment of 30.8%, larger excited state lifetime and an obvious redshift of 201 nm but also a broader absorption spectrum covering the entire visible range even up to near-IR of 1200 nm compared to JZ145. So, SPL212 can be used as a promising candidate for DSSCs. In addition, the results also prove that biscarbodithiolic acid may be more favorable than dicyanovinylsulfonic acid as acceptor group in DSSCs.

  2. TDDFT screening auxiliary withdrawing group and design the novel D-A-π-A organic dyes based on indoline dye for highly efficient dye-sensitized solar cells.

    PubMed

    Yang, Zhenqing; Liu, Yun; Liu, Chunmeng; Lin, Chundan; Shao, Changjin

    2016-10-01

    Based on the experimentally synthesized dye JZ145, we designed a series of novel D-A-π-A dyes SPL201-SPL211 with different π-conjugated bridges and a new auxiliary withdrawing group for highly efficient dye-sensitized solar cells (DSSCs) using density functional theory (DFT) and time-dependent DFT(TDDFT). The molecular structures, energy levels, absorption spectra, light-harvesting efficiency (LHE), driving force of injection(ΔGinj) and regeneration(ΔGreg), electron dipole moment (μnormal) and lifetime of the first excited state(τ) were all scrutinized in details. Results reveal that the additional withdrawing group A2 and the π-conjugated group di-η-hexyl-substituted cyclopentadithiophene (CPDT) are more promising functional groups for the organic dyes with D-A-π-A structure. We further designed SPL212 and SPL213 by employing indoline group as donor, the above screened functional groups as π-conjugated bridge and additional withdrawing group, biscarbodithiolic acid and dicyanovinyl sulfonic acid groups as acceptor group. We found that SPL212 exhibits not only a higher molar extinction coefficient with an increment of 30.8%, larger excited state lifetime and an obvious redshift of 201nm but also a broader absorption spectrum covering the entire visible range even up to near-IR of 1200nm compared to JZ145. So, SPL212 can be used as a promising candidate for DSSCs. In addition, the results also prove that biscarbodithiolic acid may be more favorable than dicyanovinylsulfonic acid as acceptor group in DSSCs. PMID:27269476

  3. Solubilization of two organic dyes by cationic ester-containing gemini surfactants.

    PubMed

    Tehrani-Bagha, A R; Singh, R G; Holmberg, K

    2012-06-15

    Solubilization of two different types of organic dyes, Quinizarin with an anthraquinone structure and Sudan I with an azo structure, has been studied in aqueous solutions of a series of cationic gemini surfactants and of a conventional monomeric cationic surfactant, dodecyltrimethylammonium bromide (DTAB). Surfactant concentrations both above and below the critical micelle concentration were used. The concentration of solubilized dye at equilibrium was determined from the absorbance of the solution at λ(max) with the aid of a calibration curve. The solubilization power of the gemini surfactants was higher than that of DTAB and increased with increasing alkyl chain length. An increase in length of the spacer unit resulted in increased solubilization power while a hydroxyl group in the spacer did not have much effect. Ester bonds in the alkyl chains reduced the solubilization power with respect to both dyes. A comparison between the absorbance spectra of the dyes in micellar solution with spectra in a range of solvents of different polarity indicated that the dye is situated in a relatively polar environment. One may therefore assume that the dye is located just below the head group region of the micelle. Attractive π-cation interactions may play a role for orienting the dye to the outer region of the micelle.

  4. Selective positioning of organic dyes in a mesoporous inorganic oxide film.

    PubMed

    Lee, Kyungtae; Park, Se Woong; Ko, Min Jae; Kim, Kyungkon; Park, Nam-Gyu

    2009-08-01

    Although sequential adsorption of dyes in a single TiO(2) electrode is ideal to extend the range of light absorption in dye-sensitized solar cells, high-temperature processing has so far limited its application. We report a method for selective positioning of organic dye molecules with different absorption ranges in a mesoporous TiO(2) film by mimicking the concept of the stationary phase and the mobile phase in column chromatography, where polystyrene-filled mesoporous TiO(2) film is explored for use as a stationary phase and a Brønsted-base-containing polymer solution is developed for use as a mobile phase for selective desorption of the adsorbed dye. By controlling the desorption and adsorption depth, yellow, red and green dyes were vertically aligned within a TiO(2) film, which is confirmed by an electron probe micro-analyser. The external quantum efficiency (EQE) spectrum from a solar cell with three selectively positioned dyes reveals the EQE characteristics of each single-dye cell. PMID:19561600

  5. Adsorption of azo dyes from aqueous solution by the hybrid MOFs/GO.

    PubMed

    Li, Ling; Shi, Zhennan; Zhu, Hongyang; Hong, Wei; Xie, Fengwei; Sun, Keke

    2016-01-01

    In this work, a hybrid of chromium(III) terephthalate metal organic framework (MIL-101) and graphene oxide (GO) was synthesized and its performance in the removal of azo dyes (Amaranth, Sunset Yellow, and Carmine) from water was evaluated. The adsorption for azo dyes on MIL-101/GO was compared with that of MIL-101, and it was found that the addition of GO enhanced the stability of MIL-101 in water and increased the adsorption capacity. The maximum adsorption capacities of MIL-101/GO were 111.01 mg g(-1) for Amaranth, 81.28 mg g(-1) for Sunset Yellow, and 77.61 mg g(-1) for Carmine. The adsorption isotherms and kinetics were investigated, showing that the adsorption fits the Freundlich isotherm and the pseudo-second-order kinetic model. The recyclability of MIL-101/GO was shown by the regeneration by acetone. The high adsorption capability and excellent reusability make MIL-101/GO a competent adsorbent for the removal dyes from aqueous solution.

  6. Enhanced fluorescence emitted by microdroplets containing organic dye emulsions.

    PubMed

    Boni, M; Nastasa, V; Andrei, I R; Staicu, Angela; Pascu, M L

    2015-01-01

    In this paper, laser beam resonant interaction with pendant microdroplets that are seeded with a laser dye (Rhodamine 6G (Rh6G)) water solution or oily Vitamin A emulsion with Rhodamine 6G solution in water is investigated through fluorescence spectra analysis. The excitation is made with the second harmonic generated beam emitted by a pulsed Nd:YAG laser system at 532 nm. The pendant microdroplets containing emulsion exhibit an enhanced fluorescence signal. This effect can be explained as being due to the scattering of light by the sub-micrometric drops of oily Vitamin A in emulsion and by the spherical geometry of the pendant droplet. The droplet acts as an optical resonator amplifying the fluorescence signal with the possibility of producing lasing effect. Here, we also investigate how Rhodamine 6G concentration, pumping laser beam energies and number of pumping laser pulses influence the fluorescence behavior. The results can be useful in optical imaging, since they can lead to the use of smaller quantities of fluorescent dyes to obtain results with the same quality. PMID:25784965

  7. Macrophages possess probenecid-inhibitable organic anion transporters that remove fluorescent dyes from the cytoplasmic matrix

    PubMed Central

    1987-01-01

    We introduced several membrane-impermeant fluorescent dyes, including Lucifer Yellow, carboxyfluorescein, and fura-2, into the cytoplasmic matrix of J774 cells and thioglycollate-elicited mouse peritoneal macrophages by ATP permeabilization of the plasma membrane and observed the subsequent fate of these dyes. The dyes did not remain within the cytoplasmic matrix; instead they were sequestered within phase-lucent cytoplasmic vacuoles and released into the extracellular medium. We used Lucifer Yellow to study these processes further. In cells incubated at 37 degrees C, 87% of Lucifer Yellow was released from the cells within 30 min after dye loading. The dye that remained within the cells at this time was predominantly within cytoplasmic vacuoles. Lucifer yellow transport was temperature dependent and occurred against a concentration gradient; therefore it appeared to be an energy- requiring process. The fluorescent dyes used in these studies are all organic anions. We therefore examined the ability of probenecid (p- [dipropylsulfamoyl]benzoic acid), which blocks organic anion transport across many epithelia, to inhibit efflux of Lucifer Yellow, and found that this drug inhibited this process in a dose-dependent and reversible manner. Efflux of Lucifer Yellow from the cells did not require Na+ co-transport or Cl- antiport; however, it was inhibited by lowering of the extracellular pH. These experiments indicate that macrophages possess probenecid-inhibitable transporters which are similar in their functional properties to organic anion transporters of epithelial cells. Such organic anion transporters have not been described previously in macrophages; they may mediate the release of naturally occurring organic anions such as prostaglandins, leukotrienes, glutathione, bilirubin, or lactate from macrophages. PMID:3693397

  8. Active polymer fibres doped with organic dyes: Generation and amplification of coherent radiation

    SciTech Connect

    Maier, G V; Kopylova, T N; Svetlichnyi, Valerii A; Podgaetskii, Vitalii M; Dolotov, S M; Ponomareva, O V; Monich, A E; Monich, E A

    2007-01-31

    The technology is developed for manufacturing active polymer optical fibres doped with organic dyes. Stimulated emission and amplification in the long-wavelength part of the visible spectrum is studied for rhodamine 11B, phenalemine 512 and substituted DCM pyran in polymer optical fibres. Lasing was observed upon longitudinal and transverse pumping by the second harmonic of a Nd:YAG laser. The gain in polymer fibres was estimated by measuring the intensity ratio of radiation of a master oscillator (dye laser) propagated through the excited (pumped) and unexcited (not pumped) fibre pieces doped with organic dyes. It is shown that the lasing efficiency of rhodamine 11B in a transversely pumped polymer fibre can achieve 36%. The maximum gain (25 dB m{sup -1}) is obtained in fibres doped with phenalemine 512. (lasers)

  9. Electronic structure measurements of metal-organic solar cell dyes using x-ray absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Johnson, Phillip S.

    The focus of this thesis is twofold: to report the results of X-ray absorption studies of metal-organic dye molecules for dye-sensitized solar cells and to provide a basic training manual on X-ray absorption spectroscopy techniques and data analysis. The purpose of our research on solar cell dyes is to work toward an understanding of the factors influencing the electronic structure of the dye: the choice of the metal, its oxidation state, ligands, and cage structure. First we study the effect of replacing Ru in several common dye structures by Fe. First-principles calculations and X-ray absorption spectroscopy at the C 1s and N 1s edges are combined to investigate transition metal dyes in octahedral and square planar N cages. Octahedral molecules are found to have a downward shift in the N 1s-to-pi* transition energy and an upward shift in C 1s-to-pi* transition energy when Ru is replaced by Fe, explained by an extra transfer of negative charge from Fe to the N ligands compared to Ru. For the square planar molecules, the behavior is more complex because of the influence of axial ligands and oxidation state. Next the crystal field parameters for a series of phthalocyanine and porphyrins dyes are systematically determined using density functional calculations and atomic multiplet calculations with polarization-dependent X-ray absorption spectra. The polarization dependence of the spectra provides information on orbital symmetries which ensures the determination of the crystal field parameters is unique. A uniform downward scaling of the calculated crystal field parameters by 5-30% is found to be necessary to best fit the spectra. This work is a part of the ongoing effort to design and test new solar cell dyes. Replacing the rare metal Ru with abundant metals like Fe would be a significant advance for dye-sensitized solar cells. Understanding the effects of changing the metal centers in these dyes in terms of optical absorption, charge transfer, and electronic

  10. An Efficient Approach Towards the Photodegradation of Indigo Carmine by Introducing ZnO/CuO/Si Ternary Nanocomposite as Photocatalyst

    NASA Astrophysics Data System (ADS)

    Dhara, Arnab; Baral, Apurba; Chabri, Sumit; Sinha, Arijit; Bandyopadhyay, Nil Ratan; Mukherjee, Nillohit

    2016-05-01

    The authors report a facile route for the large scale synthesis of CuO/ZnO/Si ternary system achieved by non-equilibrium synthesis using High Energy Ball Milling (HEBM) technique. The synthesized material was found highly efficient for the photo-degradation of a hazardous dye Indigo Carmine, a widely used dye in textile industries with major threats to our environment. The structural properties of the prepared material were evaluated using X-ray diffraction and field emission scanning electron microscopy, which revealed, that the optimization of milling duration plays a crucial role for the formation of such ternary system. UV-Vis-NIR spectroscopy yielded broadband absorption of light over the region 1100-350 nm. The photocatalytic activities of CuO/ZnO/Si ternary system were systematically explored by monitoring the fall in specific absorption peak intensity of the aqueous Indigo Carmine solution exposed under artificial light source.

  11. Photocatalytic Destruction of an Organic Dye Using TiO2 and Solar Energy.

    ERIC Educational Resources Information Center

    Giglio, Kimberly D.; And Others

    1995-01-01

    Describes a general chemistry experiment that is carried out in sunlight to illustrate the ability of TiO2 to act as a photocatalyst by mineralizing an organic dye into carbon dioxide. Details about the construction of the reactor system used to perform this experiment are included. (DDR)

  12. Optical Properties of Fluorescent Mixtures: Comparing Quantum Dots to Organic Dyes

    ERIC Educational Resources Information Center

    Hutchins, Benjamin M.; Morgan, Thomas T.; Ucak-Astarlioglu, Mine G.; Wlilliams, Mary Elizabeth

    2007-01-01

    The study describes and compares the size-dependent optical properties of organic dyes with those of semiconductor nanocrystals or quantum dots (QDs). The analysis shows that mixtures of QDs contain emission colors that are sum of the individual QD components.

  13. Rhodanine dye-based small molecule acceptors for organic photovoltaic cells.

    PubMed

    Kim, Yujeong; Song, Chang Eun; Moon, Sang-Jin; Lim, Eunhee

    2014-08-01

    The solution-processable small molecules based on carbazole or fluorene containing rhodanine dyes at both ends were synthesized and introduced as acceptors in organic photovoltaic cells. The high energy levels of their lowest unoccupied molecular orbitals resulted in a power conversion efficiency of 3.08% and an open circuit voltage of up to 1.03 V.

  14. Effect of electron withdrawing unit for dye-sensitized solar cell based on D-A-π-A organic dyes

    SciTech Connect

    Kwon, Dong Yuel; Chang, Dong Min; Kim, Young Sik

    2014-10-15

    Highlights: • To gain the red-shifted absorption spectra, withdrawing unit was substituted in dye. • By the introduction of additional withdrawing unit, LUMOs level of dye are decreased. • Decreasing LUMOs level of dye caused the red-shifted absorption spectra of dye. • Novel acceptor, DCRD, showed better photovoltaic properties than cyanoacetic acid. - Abstract: In this work, two novel D-A-π-A dye sensitizers with triarylamine as an electron donor, isoindigo and cyano group as electron withdrawing units and cyanoacetic acid and 2-(1,1-dicyanomethylene) rhodanine as an electron acceptor for an anchoring group (TICC, TICR) were designed and investigated with the ID6 dye as the reference. The difference in HOMO and LUMO levels were compared according to the presence or absence of isoindigo in ID6 (TC and ID6). To gain insight into the factors responsible for photovoltaic performance, we used density functional theory (DFT) and time-dependent density functional theory (TDDFT) calculations. Owing to different LUMO levels for each acceptor, the absorption band and molar extinction coefficient of each dye was different. Among the dyes, TICR showed more red-shifted and broader absorption spectra than other dyes and had a higher molar extinction coefficient than the reference. It is expected that TICR would show better photovoltaic properties than the other dyes, including the reference dye.

  15. Molecular engineering of D-D-π-A type organic dyes incorporating indoloquinoxaline and phenothiazine for highly efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Qian, Xing; Wang, Xiaoying; Shao, Li; Li, Hongmei; Yan, Rucai; Hou, Linxi

    2016-09-01

    Four metal-free organic dyes QX05-08 based on indoloquinoxaline and phenothiazine have been successfully designed and synthesized for dye-sensitized solar cells. The D-D-π-A type dyes QX07 and QX08 consist of an indoloquinoxaline donor, a phenothiazine donor, a cyanoacrylic acid acceptor/anchoring group and a thiophene or furan π-bridge. Other simple D-π-A type dyes QX05 and QX06 based on indoloquinoxaline and phenothiazine respectively have also been synthesized for comparison. The D-D-π-A type dyes QX07 and QX08 present good balanced structures and show excellent photoelectric properties. Especially, the dye QX07 with a thiophene unit as the π-bridge exhibits the best photovoltaic performances in solar cells. A high power conversion efficiency up to 8.28% with a Jsc of 15.3 mA cm-2 and a Voc of 757 mV have been achieved by the dye QX07 using an iodine electrolyte under standard conditions.

  16. Library of UV-Vis-NIR reflectance spectra of modern organic dyes from historic pattern-card coloured papers.

    PubMed

    Montagner, Cristina; Bacci, Mauro; Bracci, Susanna; Freeman, Rachel; Picollo, Marcello

    2011-09-01

    An accurate characterisation of the organic dyes used in artworks, especially those made of paper, is an important factor in designing safe conservation treatments. In the case of synthetic organic dyes used in modern works of art, for example, one frequently encountered difficulty is that some of these dyes are not still commercially available. Recognizing this problem, the authors of this paper present the results of an analysis of UV-Vis-NIR fibre optic reflectance spectra of 82 samples of dyed paper prepared with 41 dyes. The samples come from a historic book, The Dyeing of Paper in the Pulp, which was published by Interessen-Gemeinschaft (I.G.) Farbenindustrie in 1925. The dyes used in the paper pulp belong to the azo compounds, acridine, anthraquinone, azine, diphenylmethane, indigoid, methine, nitro, quinoline, thiazine, triphenylmethane, sulphur and xanthene classes.

  17. Use of jute processing wastes for treatment of wastewater contaminated with dye and other organics.

    PubMed

    Banerjee, Souvik; Dastidar, M G

    2005-11-01

    A study was conducted to examine the potential of jute processing waste (JPW) for the treatment of wastewater contaminated with dye and other organics generated from various activities associated with jute cultivation and fibre production. Adsorption studies in batch mode have been conducted using dye solution as an adsorbate and JPW as an adsorbent. A comparative adsorption study was made with standard adsorbents such as powdered and granular activated carbon (PAC and GAC, respectively). A maximum removal of 81.7% was obtained with methylene blue dye using JPW as compared to 61% using PAC and 40% using GAC under similar conditions. The adsorption potential of JPW was observed to be dependent on various parameters such as type of dye, initial dye concentration, pH and dosage of adsorbent. The batch sorption data conformed well to the Langmuir and Freundlich isotherms. However, lower BOD (33.3%) and COD (13.8%) removal from retting effluent was observed using JPW as compared to 75.6% BOD removal and 71.1% COD removal obtained with GAC.

  18. Organic sensitizers for dye-sensitized solar cell (DSSC): Properties from computation, progress and future perspectives

    NASA Astrophysics Data System (ADS)

    Obotowo, I. N.; Obot, I. B.; Ekpe, U. J.

    2016-10-01

    The advent of the dye-sensitized solar cells (DSSCs) came at a time when the quest for alternative energy was high, replacing p-n junction photovoltaic devices. Its uniqueness arises from the fact that unlike the conventional systems where the semiconductor assumes the task of light absorption and charge transport, the two functions are separated in DSSC. Organic sensitizers have been used to harvest a large fraction of sunlight ranging from the UV region to the near infrared region of the spectrum leading to power conversion efficiencies of up to ∼ 10.65 % for metal-free organic sensitizers. Currently, experimental analysis of photo sensitizers utilized in DSSCs is often a trial and error process, often laborious and require extensive and expensive chemical synthesis. In most cases, disappointing results from late-stage of the dye synthesis indicate an urgent need to understand the properties of the dyes at a molecular level, before experiments take place. Fortunately, the use of quantum chemical calculations especially Density Functional Theory (DFT) to screen potential dyes has helped in developing efficient sensitizers and to reduce cost. In the present review article, we discuss the current state of the field, new concepts, design strategies, challenges facing the theoretical design and development of organic sensitizers for DSSCs and future perspectives.

  19. Computational comparison of CPDT to other conjugated linkers in triarylamine-based organic dyes.

    PubMed

    Climent, Clàudia; Casanova, David

    2013-01-01

    The use of the cyclopentadithiophene (cpdt) fragment to chemically link electron donor and acceptor groups has become a rather common procedure to design new organic dyes with enhanced light harvesting properties. The photo-to-current efficiencies obtained by sensitized solar cells with dyes incorporating the cpdt moiety are commonly improved with respect to other similar π-fragments as separators. In many cases, the advantages of cpdt can be related to the larger extinction coefficients obtained. In this work we perform a detailed computational study of triarylamine-based organic dyes with the cyanoacrylic acid as the acceptor group and considering a variety of conjugated linkers with cpdt as the reference case. The influence of slightly different linkers and donor groups in the computed excitation energies and oscillator strengths is discussed by means of molecular geometries and frontier orbitals. The structural characteristics imposed by cpdt compared to similar conjugated bridges are responsible for its larger computed oscillator strengths. The insertion of an ethylene unit between the donor group and the linker systematically reduces the energy gap to the first excited singlet state and yields larger oscillator strengths of the optical transition. These results could be very helpful in the quest of new organic dyes with improved properties as sensitizers in Grätzel cells.

  20. Degradation of cyanoacrylic acid-based organic sensitizers in dye-sensitized solar cells.

    PubMed

    Chen, Cheng; Yang, Xichuan; Cheng, Ming; Zhang, Fuguo; Sun, Licheng

    2013-07-01

    Organic dyes have become widely used in dye-sensitized solar cells (DSSCs) because of their good performance, flexible structural modifications, and low costs. To increase the photostability of organic dye-based DSSCs, we conducted a full study on the degradation mechanism of cyanoacrylic acid-based organic sensitizers in DSSCs. The results showed that with the synergy between water and UV light, the sensitizer could desorb from the TiO2 surface and the cyanoacrylic acid unit of the sensitizer was transformed into the aldehyde group. It was also observed that the water content had a great effect on the degradation process. Our experiments conducted using (18) O-labeled water demonstrated that the oxygen atom of the aldehyde group identified in the degraded dye came from the solvent water in the DSSCs. Therefore, controlling the water content during DSSC fabrication, good sealing of cells, and filtering the UV light are crucial to produce DSSCs that are more durable and robust.

  1. Synthesis of Pt3Ni microspheres with high performance for rapid degradation of organic dyes.

    PubMed

    Wang, Min; Yang, Yushi; Long, Jia; Mao, Zhou; Qiu, Tong; Wu, Qingzhi; Chen, Xiaohui

    2015-12-01

    In this study, Pt3Ni microspheres consisted of nanoparticles were synthesized without addition of surfactants via the solvothermal route. The obtained sample was characterized by X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometer (ICP-AES), X-ray photoelectron spectroscopy (XPS), and field-emission scanning electron microscopy (FESEM). Furthermore, the catalytic performance of as-synthesized Pt3Ni microspheres was evaluated on the degradation of different organic dyes (methylene blue, methyl orange, Congo red, and rhodamine B). The results show that different dyes were rapidly decomposed by Pt3Ni microspheres in different pathways. Among different dyes, the formation and further degradation of the intermediates was observed during the degradation of methylene blue and methyl orange, suggesting the indirect degradation process of these dyes. This study provides not only a promising catalyst for the removal of organic contaminants for environment remediation, but also new insights for Pt3Ni alloy as a high-performance catalyst in organic synthesis.

  2. Imaging fluorescence correlation spectroscopy studies of dye diffusion in self-assembled organic nanotubes.

    PubMed

    Xu, Hao; Nagasaka, Shinobu; Kameta, Naohiro; Masuda, Mitsutoshi; Ito, Takashi; Higgins, Daniel A

    2016-06-22

    The rate and mechanism of diffusion by anionic sulforhodamine B (SRB) dye molecules within organic nanotubes self-assembled from bolaamphiphile surfactants were investigated by imaging fluorescence correlation spectroscopy (imaging-FCS). The inner and outer surfaces of the nanotubes are terminated with amine and glucose groups, respectively; the former allow for pH-dependent manipulation of nanotube surface charge while the latter enhance their biocompatibility. Wide-field fluorescence video microscopy was used to locate and image dye-doped nanotubes dispersed on a glass surface. Imaging-FCS was then used to spatially resolve the SRB transport dynamics. Mobilization of the dye molecules was achieved by immersion of the nanotubes in buffer solution. Experiments were performed in pH 6.4, 7.4 and 8.4 buffers, at ionic strengths ranging from 1.73 mM to 520 mM. The results show that coulombic interactions between cationic ammonium ions on the inner nanotube surface and the anionic SRB molecules play a critical role in governing mass transport of the dye. The apparent dye diffusion coefficient, D, was found to generally increase with increasing ionic strength and with increasing pH. The D values obtained were found to be invariant along the nanotube length. Mass transport of the SRB molecules within the nanotubes is concluded to occur by a desorption-mediated Fickian diffusion mechanism in which dye motion is slowed by its coulombic interactions with the inner surfaces of the nanotubes. The results of these studies afford information essential to the use of organic nanotubes in controlled drug release applications. PMID:27271313

  3. Photoinduced reactions between Pb3O4 and organic dyes in aqueous solution under visible light.

    PubMed

    Zhou, Yangen; Long, Jinlin; Gu, Quan; Lin, Huaxiang; Lin, Huan; Wang, Xuxu

    2012-12-01

    Pb(3)O(4) could react with organic dyes in aqueous solution under visible light irradiation, in which Pb(3)O(4) was transformed into Pb(3)(CO(3))(2)(OH)(2) along with oxidation of the organic dyes. Cu(2+) has considerable effect on the reaction. In the presence of Cu(2+), MO (20 ppm) and RhB (10(-5) mol L(-1)) were completely degraded under visible light within 6 and 20 min, respectively, while both Pb(3)O(4) and Cu(2+) keep almost stable during photodegradation. The mechanisms of the reactions with and without Cu(2+) ions were studied. The photochemical system of Pb(3)O(4) cooperating with Cu(2+) ions is probably used for the treatment of organic pollutants in water under visible light.

  4. Organic dye penetration quantification into a dental composite resin cured by LED system using fluorescence spectroscopy

    NASA Astrophysics Data System (ADS)

    Lizarelli, Rosane de Fátima Zanirato; Silva, Maciel E., Jr.; Lins, Emery C. C. C.; Costa, Mardoqueu M.; Pelino, José Eduardo P.; Bagnato, Vanderlei S.

    2007-02-01

    A major characteristic of LEDs systems is the lower heat emission related with the kind of light generation and spectral emission band. Material temperature during photoactivation can promote different photocuring performance. Organic dye penetration could be a trace to identify the efficacy of photocured composite resin. A new method using fluorescent spectroscopy through digital image evaluation was developed in this study. In order to understand if there is a real influence of material temperature during the photoactivation procedure of a dental restorative material, a hybrid composite resin (Z250, 3M-Espe, USA) and 3 light sources, halogen lamp (510 mW/cm2) and two LED systems 470+/-10nm (345 and 1000 mW/cm2) under different temperatures and intensities were used. One thousand and five hundred samples under different associations between light sources and temperatures (0, 25, 50, 75 and 100 °C were tested and immediately kept in 6G rodamin dye solution. Dye penetration was evaluated through fluorescent spectroscopy recorded by digital image data. Pixels in gray scale showed the percentage penetration of organic dye into the composite resin mass. Time and temperature were statistically significant (p<0.05) through the ANOVA statistical test. The lowest penetration value was with 60 seconds and 25 °C. Time and temperature are important factors to promote a homogeneous structure polymerized composite resin more than the light source type, halogen or LEDs system.

  5. Degradation of organic dyes by Si/SiOx core-shell nanowires: Spontaneous generation of superoxides without light irradiation.

    PubMed

    Cao, Yu; Gu, Xiaoyu; Yu, Hongkun; Zeng, Wei; Liu, Xiang; Jiang, Suhua; Li, Yuesheng

    2016-02-01

    Recently, silicon nanowires (SiNWs) have been proven to be highly active in the photocatalysis of dye degradation. However, the unstable hydrogen-terminated surface and the need for constant light irradiation hinder their extensive use. In this work, a stable silica shell was intentionally formed on the surface of SiNWs to produce Si/SiOx core-shell silicon nanowires (S-SiNWs). Light-illuminated or not, S-SiNWs showed almost identical degradation ability for the degradation of indigo carmine (IC) in both conditions, which meant neither hydrogen termination nor light irradiation was a prerequisite for the degradation activity of S-SiNWs. UV/Vis spectroscopy and liquid chromatography/mass spectrometry showed that IC was converted into isatin sulfonic acid in this process. Quenching studies and electron paramagnetic resonance spectroscopy revealed that this bleaching ability was highly dependent on superoxides. A possible mechanism was accordingly suggested. In addition, the recently discovered reductase-like activity of SiNWs can be explained by the superoxides generation.

  6. Adsorption of organic dyes on TiO2 surfaces in dye-sensitized solar cells: interplay of theory and experiment.

    PubMed

    Anselmi, Chiara; Mosconi, Edoardo; Pastore, Mariachiara; Ronca, Enrico; De Angelis, Filippo

    2012-12-14

    First-principles computer simulations can contribute to a deeper understanding of the dye/semiconductor interface lying at the heart of Dye-sensitized Solar Cells (DSCs). Here, we present the results of simulation of dye adsorption onto TiO(2) surfaces, and of their implications for the functioning of the corresponding solar cells. We propose an integrated strategy which combines FT-IR measurements with DFT calculations to individuate the energetically favorable TiO(2) adsorption mode of acetic acid, as a meaningful model for realistic organic dyes. Although we found a sizable variability in the relative stability of the considered adsorption modes with the model system and the method, a bridged bidentate structure was found to closely match the FT-IR frequency pattern, also being calculated as the most stable adsorption mode by calculations in solution. This adsorption mode was found to be the most stable binding also for realistic organic dyes bearing cyanoacrylic anchoring groups, while for a rhodanine-3-acetic acid anchoring group, an undissociated monodentate adsorption mode was found to be of comparable stability. The structural differences induced by the different anchoring groups were related to the different electron injection/recombination with oxidized dye properties which were experimentally assessed for the two classes of dyes. A stronger coupling and a possibly faster electron injection were also calculated for the bridged bidentate mode. We then investigated the adsorption mode and I(2) binding of prototype organic dyes. Car-Parrinello molecular dynamics and geometry optimizations were performed for two coumarin dyes differing by the length of the π-bridge separating the donor and acceptor moieties. We related the decreasing distance of the carbonylic oxygen from the titania to an increased I(2) concentration in proximity of the oxide surface, which might account for the different observed photovoltaic performances. The interplay between theory

  7. Supramolecular Organization of Dye Molecules in Zeolite L Channels: Synthesis, Properties, and Composite Materials.

    PubMed

    Cao, Pengpeng; Khorev, Oleg; Devaux, André; Sägesser, Lucie; Kunzmann, Andreas; Ecker, Achim; Häner, Robert; Brühwiler, Dominik; Calzaferri, Gion; Belser, Peter

    2016-03-14

    Sequential insertion of different dyes into the 1D channels of zeolite L (ZL) leads to supramolecular sandwich structures and allows the formation of sophisticated antenna composites for light harvesting, transport, and trapping. The synthesis and properties of dye molecules, host materials, composites, and composites embedded in polymer matrices, including two- and three-color antenna systems, are described. Perylene diimide (PDI) dyes are an important class of chromophores and are of great interest for the synthesis of artificial antenna systems. They are especially well suited to advancing our understanding of the structure-transport relationship in ZL because their core fits tightly through the 12-ring channel opening. The substituents at both ends of the PDIs can be varied to a large extent without influencing their electronic absorption and fluorescence spectra. The intercalation/insertion of 17 PDIs, 2 terrylenes, and 1 quaterrylene into ZL are compared and their interactions with the inner surface of the ZL nanochannels discussed. ZL crystals of about 500 nm in size have been used because they meet the criteria that must be respected for the preparation of antenna composites for light harvesting, transport, and trapping. The photostability of dyes is considerably improved by inserting them into the ZL channels because the guests are protected by being confined. Plugging the channel entrances, so that the guests cannot escape into the environment is a prerequisite for achieving long-term stability of composites embedded in an organic matrix. Successful methods to achieve this goal are described. Finally, the embedding of dye-ZL composites in polymer matrices, while maintaining optical transparency, is reported. These results facilitate the rational design of advanced dye-zeolite composite materials and provide powerful tools for further developing and understanding artificial antenna systems, which are among the most fascinating subjects of current

  8. Blue natural organic dyestuffs--from textile dyeing to mural painting. Separation and characterization of coloring matters present in elderberry, logwood and indigo.

    PubMed

    Pawlak, Katarzyna; Puchalska, Maria; Miszczak, Agata; Rosłoniec, Elzbieta; Jarosz, Maciej

    2006-05-01

    Natural dyestuffs used for painting or dyeing of textiles are complex mixtures of compounds of various chemical properties. Proper identification of the dye used by a painter and, even better, its origin is possible only when its compositional 'fingerprint' can be evaluated. For this reason gradient program for liquid chromatographic separation of 16 color compounds--components of natural blue dyes: elderberry, logwood and indigo--has been developed. Two detector systems were used simultaneously: UV-Vis spectrophotometry (at 280, 445, 520 and 600 nm) and ESI mass spectrometry (positive and negative SIM mode). It was found that fragmentation observed in ESI-MS is affected not only by ion source parameters, but also by chromatographic conditions, especially in case of the less stable substances: cyanidin glucosides, tannic acid, rutin and hematoxylin. Examination of characteristic dissociation pathways of the compounds under investigation after direct admission into ion source or after chromatographic separation allowed to select proper ions for SIM detection and to develop novel and efficient reversed phase high performance liquid chromatographic (RP-HPLC)-UV-Vis/ESI-MS method for the analysis of natural blue dyes. The procedure was successfully applied for identification of indigotin and carminic acid-main colorants extracted from a fiber taken from the blue-red 'Italian' tapestry (the collection of the National Museum in Warsaw, Poland). PMID:16575781

  9. Proficiency of acceptor-donor-acceptor organic dye with spiro-MeOTAD HTM on the photovoltaic performance of dye sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Ramavenkateswari, K.; Venkatachalam, P.

    2016-08-01

    This work investigates the proficiency of acceptor-donor-acceptor (A-D-A) organic dye Diisopropyl azodicarboxylate (DIAC) as photosensitizer on the photovoltaic parameters of silver (Ag) doped TiO2 photoanode dye-sensitized solar cells (DSSCs) with quasi-solid state electrolyte/hole transport material (HTM) spiro-MeOTAD. TNSs (TiO2 nanosticks) photoanodes are prepared through sol-gel method and hydrothermal technique. X-ray powder diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and BET measurement were used to characterize the structure and morphology of TiO2 nanostructures. The Diisopropyl azodicarboxylate organic dye with TNPs-Ag@TNSs composite photoanode structure and spiro-MeOTAD HTM exhibited better power conversion efficiency (PCE). [Figure not available: see fulltext.

  10. Proficiency of acceptor-donor-acceptor organic dye with spiro-MeOTAD HTM on the photovoltaic performance of dye sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Ramavenkateswari, K.; Venkatachalam, P.

    2016-09-01

    This work investigates the proficiency of acceptor-donor-acceptor (A-D-A) organic dye Diisopropyl azodicarboxylate (DIAC) as photosensitizer on the photovoltaic parameters of silver (Ag) doped TiO2 photoanode dye-sensitized solar cells (DSSCs) with quasi-solid state electrolyte/hole transport material (HTM) spiro-MeOTAD. TNSs (TiO2 nanosticks) photoanodes are prepared through sol-gel method and hydrothermal technique. X-ray powder diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and BET measurement were used to characterize the structure and morphology of TiO2 nanostructures. The Diisopropyl azodicarboxylate organic dye with TNPs-Ag@TNSs composite photoanode structure and spiro-MeOTAD HTM exhibited better power conversion efficiency (PCE).

  11. Liquid chromatographic determination of carminic acid in yogurt.

    PubMed

    Jalón, M; Peña, M J; Rivas, J C

    1989-01-01

    A reverse-phase liquid chromatographic method is described for the determination of carminic acid in yogurt. A C18 column is used with acetonitrile-1.19M formic acid (19 + 81) as mobile phase and diode array detection. Sample preparation includes deproteinization with papain and purification in a polyamide column. The relative standard deviation for repeated determinations of carminic acid in a commercial strawberry-flavored yogurt was 3.0%. Recoveries of carminic acid added to a natural-flavored yogurt ranged from 87.2 to 95.3% with a mean of 90.2%. The method permits measurement of amounts as low as 0.10 mg/kg. PMID:2708269

  12. A Robust Organic Dye for Dye Sensitized Solar Cells Based on Iodine/Iodide Electrolytes Combining High Efficiency and Outstanding Stability

    PubMed Central

    Joly, Damien; Pellejà, Laia; Narbey, Stéphanie; Oswald, Frédéric; Chiron, Julien; Clifford, John N.; Palomares, Emilio; Demadrille, Renaud

    2014-01-01

    Among the new photovoltaic technologies, the Dye-Sensitized Solar Cell (DSC) is becoming a realistic approach towards energy markets such as BIPV (Building Integrated PhotoVoltaics). In order to improve the performances of DSCs and to increase their commercial attractiveness, cheap, colourful, stable and highly efficient ruthenium-free dyes must be developed. Here we report the synthesis and complete characterization of a new purely organic sensitizer (RK1) that can be prepared and synthetically upscaled rapidly. Solar cells containing this orange dye show a power conversion efficiency of 10.2% under standard conditions (AM 1.5G, 1000 Wm−2) using iodine/iodide as the electrolyte redox shuttle in the electrolyte, which is among the few examples of DSC using an organic dyes and iodine/iodide red/ox pair to overcome the 10% efficiency barrier. We demonstrate that the combination of this dye with an ionic liquid electrolyte allows the fabrication of solar cells that show power conversion efficiencies of up to 7.36% that are highly stable with no measurable degradation of initial performances after 2200 h of light soaking at 65°C under standard irradiation conditions. RK1 achieves one of the best output power conversion efficiencies for a solar cell based on the iodine/iodide electrolyte, combining high efficiency and outstanding stability. PMID:24504344

  13. A Robust Organic Dye for Dye Sensitized Solar Cells Based on Iodine/Iodide Electrolytes Combining High Efficiency and Outstanding Stability

    NASA Astrophysics Data System (ADS)

    Joly, Damien; Pellejà, Laia; Narbey, Stéphanie; Oswald, Frédéric; Chiron, Julien; Clifford, John N.; Palomares, Emilio; Demadrille, Renaud

    2014-02-01

    Among the new photovoltaic technologies, the Dye-Sensitized Solar Cell (DSC) is becoming a realistic approach towards energy markets such as BIPV (Building Integrated PhotoVoltaics). In order to improve the performances of DSCs and to increase their commercial attractiveness, cheap, colourful, stable and highly efficient ruthenium-free dyes must be developed. Here we report the synthesis and complete characterization of a new purely organic sensitizer (RK1) that can be prepared and synthetically upscaled rapidly. Solar cells containing this orange dye show a power conversion efficiency of 10.2% under standard conditions (AM 1.5G, 1000 Wm-2) using iodine/iodide as the electrolyte redox shuttle in the electrolyte, which is among the few examples of DSC using an organic dyes and iodine/iodide red/ox pair to overcome the 10% efficiency barrier. We demonstrate that the combination of this dye with an ionic liquid electrolyte allows the fabrication of solar cells that show power conversion efficiencies of up to 7.36% that are highly stable with no measurable degradation of initial performances after 2200 h of light soaking at 65°C under standard irradiation conditions. RK1 achieves one of the best output power conversion efficiencies for a solar cell based on the iodine/iodide electrolyte, combining high efficiency and outstanding stability.

  14. A robust organic dye for dye sensitized solar cells based on iodine/iodide electrolytes combining high efficiency and outstanding stability.

    PubMed

    Joly, Damien; Pellejà, Laia; Narbey, Stéphanie; Oswald, Frédéric; Chiron, Julien; Clifford, John N; Palomares, Emilio; Demadrille, Renaud

    2014-02-07

    Among the new photovoltaic technologies, the Dye-Sensitized Solar Cell (DSC) is becoming a realistic approach towards energy markets such as BIPV (Building Integrated PhotoVoltaics). In order to improve the performances of DSCs and to increase their commercial attractiveness, cheap, colourful, stable and highly efficient ruthenium-free dyes must be developed. Here we report the synthesis and complete characterization of a new purely organic sensitizer (RK1) that can be prepared and synthetically upscaled rapidly. Solar cells containing this orange dye show a power conversion efficiency of 10.2% under standard conditions (AM 1.5G, 1000 Wm(-2)) using iodine/iodide as the electrolyte redox shuttle in the electrolyte, which is among the few examples of DSC using an organic dyes and iodine/iodide red/ox pair to overcome the 10% efficiency barrier. We demonstrate that the combination of this dye with an ionic liquid electrolyte allows the fabrication of solar cells that show power conversion efficiencies of up to 7.36% that are highly stable with no measurable degradation of initial performances after 2200 h of light soaking at 65°C under standard irradiation conditions. RK1 achieves one of the best output power conversion efficiencies for a solar cell based on the iodine/iodide electrolyte, combining high efficiency and outstanding stability.

  15. Spatial modulation spectroscopy for imaging and quantitative analysis of single dye-doped organic nanoparticles inside cells.

    PubMed

    Devadas, Mary Sajini; Devkota, Tuphan; Guha, Samit; Shaw, Scott K; Smith, Bradley D; Hartland, Gregory V

    2015-06-01

    Imaging of non-fluorescent nanoparticles in complex biological environments, such as the cell cytosol, is a challenging problem. For metal nanoparticles, Rayleigh scattering methods can be used, but for organic nanoparticles, such as dye-doped polymer beads or lipid nanoparticles, light scattering does not provide good contrast. In this paper, spatial modulation spectroscopy (SMS) is used to image single organic nanoparticles doped with non-fluorescent, near-IR croconaine dye. SMS is a quantitative imaging technique that yields the absolute extinction cross-section of the nanoparticles, which can be used to determine the number of dye molecules per particle. SMS images were recorded for particles within EMT-6 breast cancer cells. The measurements allowed mapping of the nanoparticle location and the amount of dye in a single cell. The results demonstrate how SMS can facilitate efforts to optimize dye-doped nanoparticles for effective photothermal therapy of cancer.

  16. Theoretical analysis of the solvatochromism of organic dyes differing by the conjugation sequence

    NASA Astrophysics Data System (ADS)

    Manzhos, Sergei; Komatsu, Makoto; Nakazaki, Jotaro; Segawa, Hiroshi; Yamashita, Koichi

    2012-01-01

    Absorption peak maxima of two organic dyes differing by the position of the methine unit differ by 61 nm in dioxane and by up to 139 nm in polar solvents. It was previously reported that the difference is not reproduced by time-dependent density functional theory (TDDFT) using ab initio or hybrid functionals. TDDFT errors are different between the molecules, leading to a qualitative failure of TDDFT to predict relative energetics of the dyes. We focus on the effect of polar solvents (acetonitrile, DMSO, methanol, and 2-propanol) on the absorption spectrum, specifically, on the different between the two molecules sign of the solvatochromic shift versus dioxane. Using the correction due to Peach et al., the absolute TDDFT errors can be brought within acceptable ranges of 0.2 to 0.3 eV, and the blue shift versus dioxane is reproduced, although both dyes are predicted to exhibit positive solvatochromism. The inclusion of explicit solvent molecules did not appreciably change either TDDFT energies or the correction term. These results show that in dye design by changing the conjugation order, computational errors are expected to be more important than in the case of an extension of the size of conjugation, especially when polar solvents are used.

  17. Facile microwave-assisted synthesis of titanium dioxide decorated graphene nanocomposite for photodegradation of organic dyes

    SciTech Connect

    Gayathri, Shunmugiah; Kottaisamy, Muniasamy; Ramakrishnan, Veerabahu

    2015-12-15

    An efficient and facile method was adopted to prepare TiO{sub 2}-graphene (TG) nanocomposites with TiO{sub 2} nanoparticles uniformly distributed on graphene. By adjusting the amount of TiO{sub 2} precursor, both high and low dense TiO{sub 2} nanoparticles on graphene were effectively attained via electrostatic attraction between graphene oxide sheets and TiO{sub 2} nanoparticles. The prepared nanocomposites were characterized by various characterization techniques. The TG nanocomposite showed an excellent activity for the photodegradation of the organic dyes such as methylene blue (MB) and rose bengal (RB) under ultra violet (UV) light irradiation. The TG nanocomposite of TG 2.5 showed better photocatalytic performance than bare TiO{sub 2} nanoparticles and other composites. The enhanced activity of the composite material is attributed to the reduction in charge recombination and interaction of organic dyes with graphene. The decrease in charge recombination was evidenced from the photoluminescence (PL) spectra. The observed results suggest that the synthesized TG composites have a potential application to treat the industrial effluents, which contain organic dyes.

  18. The study of synthetic food dyes by positron annihilation lifetime spectroscopy.

    NASA Astrophysics Data System (ADS)

    Pivtsaev, A. A.; Razov, V. I.

    2015-06-01

    By method of positron annihilation lifetime spectroscopy (PALS), substances are food dyes were studied: E-102 (Tartrazine), E-124 (Ponso 4R), E 132 (Indigo carmine), E-133 (Brilliant Blue), E-151 (Black Shiny). They are examined for the presence of carcinogenic properties. The difference between dyes having explicit carcinogenic properties and mutagenic properties (non-explicit carcinogens) is established.

  19. Novel thiazolo[5,4-d]thiazole-based organic dyes for quasi-solid-state dye-sensitized solar cells.

    PubMed

    Zhang, Weiyi; Feng, Quanyou; Wang, Zhong-Sheng; Zhou, Gang

    2013-05-01

    A series of novel metal-free organic dyes containing the thiazolo[5,4-d]thiazole moiety were designed and synthesized for quasi-solid-state dye-sensitized solar cells (DSSCs). Different alkoxy chains were introduced into the electron donor part of the dye molecules for comparison. The optical, electrochemical, and photovoltaic properties for all sensitizers were systematically investigated. It was found that the sensitizers with the different alkoxy groups have similar photophysical and electrochemical properties, such as absorbance and energy levels, owing to their close chemical structures. However, the quasi-solid-state DSSCs based on the resulting sensitizers exhibit different performance parameters. The quasi-solid-state DSSC based on sensitizer FNE74 with two octyloxy chains possessed the highest solar energy conversion efficiency of 5.10 % under standard AM 1.5G sunlight illumination without the use of coadsorbant agents.

  20. High-performance liquid chromatographic separation of carminic acid, alpha- and beta-bixin, and alpha- and beta-norbixin, and the determination of carminic acid in foods.

    PubMed

    Lancaster, F E; Lawrence, J F

    1996-05-01

    During a study of natural food colours, a simple and reliable high-performance liquid chromatography system was developed for use with cochineal and annato. An isocratic mobile phase, consisting of methanol and 6% aqueous acetic acid, resolved bixin and norbixin, while a gradient system was used to separate carminic acid and the annato compounds. The carminic acid contents of cochineal extract, carmine and carmine hydrosoluble were determined using an isocratic mobile phase (40:60, v/v). The detection limit for carminic acid in the various products was approximately 100 ng/g. Carminic acid was determined quantitatively in fruit beverages, yogurt and candies. It was demonstrated that, because of decomposition, carminic acid was not suitable for use in candies when manufacturing temperatures above 100 degrees C were required. Most membrane filters are not suitable for use with cochineal solutions, but a cellulose membrane filter did not adsorb carminic acid and was used successfully to remove impurities from water-based cochineal products and food extracts containing carminic acid. PMID:8653204

  1. Stability of fluorescent labels in PLGA polymeric nanoparticles: Quantum dots versus organic dyes.

    PubMed

    Abdel-Mottaleb, Mona M A; Beduneau, Arnaud; Pellequer, Yann; Lamprecht, Alf

    2015-10-15

    Polymeric nanoparticles (NPs) are currently being investigated for various therapeutic, diagnostic and drug delivery applications. The study of their interactions and fate in biological systems is frequently performed via their fluorescent labeling and following them using fluorescent microscopy. Quantum dots are proposed as stable fluorescent label and compared to other organic dyes (Nile red and DiI) in terms of their entrapment, diffusion in different aqueous or lipophilic media and photostability. In vitro transfer to hydrophilic PBS solution showed that after 8h, 4.2±2.2, 15.5±2.0 and 0.9±0.02% was released from the QDs, NR and DiI nanoparticles, respectively. However, higher diffusion rates were observed in the lipophilic medium chain triglyceride and artificial sebum for all the dyes used. Fluorescent intensity of the three different markers was found to be stable over a period of 24h. Continuous illumination with laser beam using a confocal laser scanning microscopy indicated the superior stability of quantum dots compared to the other organic dyes. Skin permeation experiments have shown that QDs were the most representative marker for the polymeric nanoparticles skin penetration. PMID:26307264

  2. High effective adsorption of organic dyes on magnetic cellulose beads entrapping activated carbon.

    PubMed

    Luo, Xiaogang; Zhang, Lina

    2009-11-15

    Maghemite (gamma-Fe(2)O(3)) nanoparticles were created with a submerged circulation impinging stream reactor (SCISR) from FeCl(3) x 6H(2)O and FeCl(2).4H(2)O by using precipitation followed by oxidation. Subsequently, by blending cellulose with the Fe(2)O(3) nanoparticles and activated carbon (AC) in 7 wt% NaOH/12 wt% urea aqueous solution pre-cooled to -12 degrees C, millimeter-scale magnetic cellulose beads, coded as MCB-AC, was fabricated via an optimal dropping technology. The cellulose beads containning Fe(2)O(3) nanoparticles exhibited sensitive magnetic response, and their recovery could facilitate by applying a magnetic field. The adsorption and desorption of the organic dyes on MCB-AC were investigated to evaluate the removal of dyes (methyl orange and methylene blue) with different charges from aqueous solution. Their adsorption kinetics experiments were carried out and the data were well fitted by a pseudo-second-order equation. The results revealed that the MCB-AC sorbent could efficiently adsorb the organic dyes from wastewater, and the used sorbents could be recovered completely. Therefore, we developed a highly efficient sorbent, which were prepared by using simple and "green" process, for the applications on the removal of hazardous materials.

  3. Highly oriented surface-growth and covalent dye labeling of mesoporous metal-organic frameworks.

    PubMed

    Hinterholzinger, Florian M; Wuttke, Stefan; Roy, Pascal; Preusse, Thomas; Schaate, Andreas; Behrens, Peter; Godt, Adelheid; Bein, Thomas

    2012-04-14

    Mesoporous amino-functionalized metal-organic framework thin films with the UiO-68 topology were grown in a highly oriented fashion on two different self-assembled monolayers on gold. The oriented MOF films were covalently modified with the fluorescent dye Rhodamine B inside the pore system, as demonstrated with size-selective fluorescence quenching studies. Our study suggests that mesoporous metal-organic frameworks are promising hosts for the covalent attachment of numerous functional moieties in a molecularly designed crystalline environment.

  4. Visible light assisted degradation of organic dye using Ag3PO4

    NASA Astrophysics Data System (ADS)

    Dhanabal, R.; Velmathi, S.; Bose, A. Chandra

    2015-06-01

    The study of visible light photodegradation of organic dye Methylene Blue (MB) have been investigated using silver phosphate (Ag3PO4) as a photocatalyst which is good efficient material for photocatalytic reaction. The simple ion-exchange method is used to prepare Ag3PO4. The structure of the material have been confirmed using X-ray diffraction which shows cubic structure of Ag3PO4. The functional group of the Ag3PO4 has been verified by Fourier transform infrared spectroscopy. The bandgap of Ag3PO4 is calculated using kubelka-munk function from the ultra violet-visible diffuse reflectance spectroscopy, the absorption of Ag3PO4 starts from 470 nm. Under simulated visible light irradiation, Ag3PO4 catalyst exhibits good catalytic ability for degrading MB dye.

  5. Metal-organic frameworks at interfaces in dye-sensitized solar cells.

    PubMed

    Li, Yafeng; Chen, Caiyun; Sun, Xun; Dou, Jie; Wei, Mingdeng

    2014-09-01

    ZIF-8, a kind of widely studied metal-organic frameworks, was used for the interfacial modification of dye-sensitized solar cells by a facile post-treatment strategy for the first time, which solved the problem of severely decreased short-circuit photocurrent in previous report. After the surface treatment, the performance of cells was obviously improved. The conditions for the deposition of ZIF-8 were optimized. The best photovoltaic property was obtained when the growth time of ZIF-8 was 7 min and the TiO2 photoanode was post-treated for 2 times. Besides the energy barrier effect of ZIF-8 that improved the open-circuit photovoltage and electron lifetime, the dyes adsorbed tightly on TiO2 surface was found to be a key point for the efficient electron injection and improved performance.

  6. Organic nanofibers from squarylium dyes: local morphology, optical, and electrical properties

    NASA Astrophysics Data System (ADS)

    Balzer, Frank; Schiek, Manuela; Osadnik, Andreas; Lützen, Arne; Rubahn, Horst-Günter

    2012-02-01

    Environmentally stable, non-toxic squarylium dyes with strong absorption maxima in the red and near infrared spectral region are known for almost fifty years. Despite the fact that their optoelectronic properties distinguish them as promising materials for organics based photovoltaic cells, they have regained attention only very recently. For their application in heterojunction solar cells knowledge of their nanoscopic morphology as well as nanoscopic electrical properties is paramount. In this paper thin films from two different squarylium dyes, from squarylium (SQ) and from hydroxy-squarylium (SQOH) are investigated. The thin films are either solution casted or vacuum sublimed onto substrates such as muscovite mica, which are known to promote self-assembly into oriented, crystalline nanostructures such as nanofibers. Local characterization is performed via (polarized) optical microscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), and Kelvin probe force microscopy (KPFM).

  7. Quantum dot and quantum dot-dye co-sensitized solar cells containing organic thiolate-disulfide redox electrolyte

    NASA Astrophysics Data System (ADS)

    Meng, Ke; Surolia, Praveen K.; Byrne, Owen; Thampi, K. Ravindranathan

    2015-02-01

    Quantum dot sensitized solar cells (QDSSCs) require special electrolytes, which are not always compatible with the requirements of dye sensitized solar cells. CdS and PbS quantum dot sensitized solar cells are able to show promising power conversion efficiencies in the presence of an organic thiolate/disulfide redox electrolyte. Also, an appreciable enhancement in performance is noticed when such devices are co-sensitized with a Ru-dye. The measured cell efficiencies of the CdS/dye and PbS/dye co-sensitized solar cells are 3.93% and 4.18%, respectively, which are higher than the sum of the corresponding individual QDSSCs and the dye sensitized solar cell (DSSCs). The enhancement seen with co-sensitization was investigated and explained by the fact that it suppressed back electron transfer processes in the cell, which was ascertained by electrochemical impedance spectroscopy (EIS) results.

  8. 21 CFR 73.1100 - Cochineal extract; carmine.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Cochineal extract; carmine. 73.1100 Section 73.1100 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL... suitable and that are listed in this subpart as safe in color additive mixtures for coloring drugs....

  9. Third-order nonlinear optical response of indigo carmine under 633 nm excitation for nonlinear optical applications

    NASA Astrophysics Data System (ADS)

    Pramodini, S.; Poornesh, P.

    2014-11-01

    We report thermally induced third-order nonlinearity and optical limiting behaviour of Indigo Carmine dye. z-Scan technique was used to determine the sign and magnitude of absorptive and refractive nonlinearities. Continuous wave (CW) He-Ne laser operating at 633 nm was used as source of excitation. In open aperture z-scan experiments, samples exhibited reverse saturable absorption (RSA) process. For closed aperture z-scan experiments, samples revealed self-defocusing property. The presence of donor and acceptor groups in the structure increases the conjugation length and in turn increases the optical nonlinearity. Induced self-diffraction rings pattern was recorded for the samples and it is attributed to refractive index change and thermal lensing. Also, optical limiting and clamping studies were carried out for various input power. Optical clamping of about ~1 mW was observed. This endorses that the dye under investigation is a positive candidate for opto-electronic and photonic applications.

  10. Highly sensitive wavelength-dependent nonaqueous capillary electrophoresis for simultaneous screening of various synthetic organic dyes.

    PubMed

    Park, Moonhee; Bahng, Seung-Hoon; Woo, Nain; Kang, Seong Ho

    2016-05-15

    A novel multi-wavelength nonaqueous capillary electrophoresis (MW-NACE) technique based on wavelength-dependent laser-induced fluorescence (LIF) detection was investigated for the simultaneous screening of various synthetic organic dyes. Multi-wavelength excitation light sources were utilized to excite different organic dyes [e.g., 543 nm for crystal violet (CV), methyl violet B (MVB), methyl violet B base (MBB), rhodamine 6G (R6G), and rhodamine B base (RBB); 635 nm for nile blue A (NBA) and methylene blue (MB)] simultaneously. Using a nonaqueous buffer system composed of 15 mM sodium borate and 835 mM acetic acid in 100% ethanol (pH=5.4), all dyes were analyzed within 15 min with excellent resolution (R≥4.0) under an electric field of 500 V/cm. Calibration curves showed excellent linearity with square of correlation coefficients (r(2)) greater than 0.9908 over wide dynamic ranges of 0.4-50 μM for CV, 0.8-50 μM for MVB, 1.5-50 μM for MBB, 0.08-5 nM for R6G, 0.06-10 μM for MB, 0.02-10 μM for NBA, and 0.13-10 pM for RBB. The detection limits (S/N=3) of 40 fM to 0.5 μM were 10-200,000 times lower than those of previous detection methods. While adjacent peaks were not well distinguished with baseline separation in a single capillary, the devised technique was faster and more sensitive than conventional aqueous and nonaqueous CE approaches, thereby enabling the quantitative analysis of various dyes based on wavelength-dependent fluorescence detection with different excitation wavelengths. PMID:26992516

  11. Rapid Synthesis of Thiophene-Based, Organic Dyes for Dye-Sensitized Solar Cells (DSSCs) by a One-Pot, Four-Component Coupling Approach.

    PubMed

    Matsumura, Keisuke; Yoshizaki, Soichi; Maitani, Masato M; Wada, Yuji; Ogomi, Yuhei; Hayase, Shuzi; Kaiho, Tatsuo; Fuse, Shinichiro; Tanaka, Hiroshi; Takahashi, Takashi

    2015-06-26

    This one-pot, four-component coupling approach (Suzuki-Miyaura coupling/C-H direct arylation/Knoevenagel condensation) was developed for the rapid synthesis of thiophene-based organic dyes for dye-sensitized solar cells (DSSCs). Seven thiophene-based, organic dyes of various donor structures with/without the use of a 3,4-ethylenedioxythiophene (EDOT) moiety were successfully synthesized in good yields based on a readily available thiophene boronic acid pinacol ester scaffold (one-pot, 3-step, 35-61%). Evaluation of the photovoltaic properties of the solar cells that were prepared using the synthesized dyes revealed that the introduction of an EDOT structure beside a cyanoacrylic acid moiety improved the short-circuit current (Jsc) while decreasing the fill factor (FF). The donor structure significantly influenced the open-circuit voltage (Voc), the FF, and the power conversion efficiency (PCE). The use of a n-hexyloxyphenyl amine donor, and our originally developed, rigid, and nonplanar donor, both promoted good cell performance (η=5.2-5.6%).

  12. Cosensitization of D-A-π-A quinoxaline organic dye: efficiently filling the absorption valley with high photovoltaic efficiency.

    PubMed

    Pei, Kai; Wu, Yongzhen; Li, Hui; Geng, Zhiyuan; Tian, He; Zhu, Wei-Hong

    2015-03-11

    In the efficient cosensitization, the pure organic sensitizers with high molecular extinction coefficients and long wavelength response are highly preferable since the dye loading amount for each dye in cosensitization is decreased with respect to single dye sensitization. A D-A-π-A featured quinoxaline organic sensitizer IQ21 is specifically designed. The high conjugation building block of 4H-cyclopenta[2,1-b:3,4-b']dithiophene (CPDT) is introduced as the π bridge, instead of the traditional thiophene unit, especially in realizing high molecular extinction coefficients (up to 66 600 M(-1) cm(-1)) and extending the light response wavelength. With respect to the reference dye IQ4, the slightly lower efficiency of IQ21 (9.03%) arises from the decrease of VOC, which offsets the gain in JSC. While cosensitized with a smaller D-π-A dye S2, the efficiency in IQ21 is further improved to 10.41% (JSC = 19.8 mA cm(-2), VOC = 731 mV, FF = 0.72). The large improvement in efficiency is attributed to the well-matched molecular structures and loading amounts of both dyes in the cosensitization system. We also demonstrated that coabsorbent dye S2 can distinctly compensate the inherent drawbacks of IQ21, not only enhancing the response intensity of IPCE, making up the absorption defects around low wavelength region of IPCE, but also repressing the charge recombination rate to some extent.

  13. Spatial modulation spectroscopy for imaging and quantitative analysis of single dye-doped organic nanoparticles inside cells

    NASA Astrophysics Data System (ADS)

    Devadas, Mary Sajini; Devkota, Tuphan; Guha, Samit; Shaw, Scott K.; Smith, Bradley D.; Hartland, Gregory V.

    2015-05-01

    Imaging of non-fluorescent nanoparticles in complex biological environments, such as the cell cytosol, is a challenging problem. For metal nanoparticles, Rayleigh scattering methods can be used, but for organic nanoparticles, such as dye-doped polymer beads or lipid nanoparticles, light scattering does not provide good contrast. In this paper, spatial modulation spectroscopy (SMS) is used to image single organic nanoparticles doped with non-fluorescent, near-IR croconaine dye. SMS is a quantitative imaging technique that yields the absolute extinction cross-section of the nanoparticles, which can be used to determine the number of dye molecules per particle. SMS images were recorded for particles within EMT-6 breast cancer cells. The measurements allowed mapping of the nanoparticle location and the amount of dye in a single cell. The results demonstrate how SMS can facilitate efforts to optimize dye-doped nanoparticles for effective photothermal therapy of cancer.Imaging of non-fluorescent nanoparticles in complex biological environments, such as the cell cytosol, is a challenging problem. For metal nanoparticles, Rayleigh scattering methods can be used, but for organic nanoparticles, such as dye-doped polymer beads or lipid nanoparticles, light scattering does not provide good contrast. In this paper, spatial modulation spectroscopy (SMS) is used to image single organic nanoparticles doped with non-fluorescent, near-IR croconaine dye. SMS is a quantitative imaging technique that yields the absolute extinction cross-section of the nanoparticles, which can be used to determine the number of dye molecules per particle. SMS images were recorded for particles within EMT-6 breast cancer cells. The measurements allowed mapping of the nanoparticle location and the amount of dye in a single cell. The results demonstrate how SMS can facilitate efforts to optimize dye-doped nanoparticles for effective photothermal therapy of cancer. Electronic supplementary information (ESI

  14. Metal-organic gel templated synthesis of magnetic porous carbon for highly efficient removal of organic dyes.

    PubMed

    Wang, Luhuan; Ke, Fei; Zhu, Junfa

    2016-03-21

    Magnetic porous carbon composites are promising materials in various applications, such as adsorbents, supercapacitors and catalyst supports, due to their high surface area, thermal and chemical stability, and easy separation. However, despite the increasing number of reports of magnetic porous carbon composites, the preparation of these materials with environmentally friendly procedures still remains a great challenge. Herein, we report a facile method to prepare a magnetic porous carbon composite with high surface area from a Fe-based metal-organic gel (MOG) template, an extended structure of a metal-organic framework (MOF). The obtained magnetic porous carbon composite was applied to remove organic dyes from an aqueous solution by selecting methyl orange (MO) as a model molecule. It exhibits excellent adsorption capacity (182.82 mg g(-1)), fast adsorption kinetics (8.13 × 10(-3) g mg(-1) min(-1)), and a perfect magnetic separation performance for the MO removal. This study demonstrates a new way to achieve clean synthesis of magnetic porous carbon materials, and opens a new door for the application of MOGs in organic dye removal.

  15. Synthesis of Organic Dye-Impregnated Silica Shell-Coated Iron Oxide Nanoparticles by a New Method

    NASA Astrophysics Data System (ADS)

    Ren, Cuiling; Li, Jinhua; Liu, Qian; Ren, Juan; Chen, Xingguo; Hu, Zhide; Xue, Desheng

    2008-12-01

    A new method for preparing magnetic iron oxide nanoparticles coated by organic dye-doped silica shell was developed in this article. Iron oxide nanoparticles were first coated with dye-impregnated silica shell by the hydrolysis of hexadecyltrimethoxysilane (HTMOS) which produced a hydrophobic core for the entrapment of organic dye molecules. Then, the particles were coated with a hydrophilic shell by the hydrolysis of tetraethylorthosilicate (TEOS), which enabled water dispersal of the resulting nanoparticles. The final product was characterized by X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, photoluminescence spectroscopy, and vibration sample magnetometer. All the characterization results proved the final samples possessed magnetic and fluorescent properties simultaneously. And this new multifunctional nanomaterial possessed high photostability and minimal dye leakage.

  16. Degradation of organic dyes via bismuth silver oxide initiated direct oxidation coupled with sodium bismuthate based visible light photocatalysis.

    PubMed

    Yu, Kai; Yang, Shaogui; Liu, Cun; Chen, Hongzhe; Li, Hui; Sun, Cheng; Boyd, Stephen A

    2012-07-01

    Organic dye degradation was achieved via direct oxidation by bismuth silver oxide coupled with visible light photocatalysis by sodium bismuthate. Crystal violet dye decomposition by each reagent proceeded via two distinct pathways, each involving different active oxygen species. A comparison of each treatment method alone and in combination demonstrated that using the combined methods in sequence achieved a higher degree of degradation, and especially mineralization, than that obtained using either method alone. In the combined process direct oxidation acts as a pretreatment to rapidly bleach the dye solution which substantially facilitates subsequent visible light photocatalytic processes. The integrated sequential direct oxidation and visible light photocatalysis are complementary manifesting a > 100% increase in TOC removal, compared to either isolated method. The combined process is proposed as a novel and effective technology based on one primary material, sodium bismuthate, for treating wastewaters contaminated by high concentrations of organic dyes.

  17. Identification of natural dyes in archeological Coptic textiles by liquid chromatography with diode array detection.

    PubMed

    Orska-Gawryś, Jowita; Surowiec, Izabella; Kehl, Jerzy; Rejniak, Hanna; Urbaniak-Walczak, Katarzyna; Trojanowicz, Marek

    2003-03-14

    Reversed-phase HPLC with diode-array UV-Vis spectrophotometric detection has been used for identification of natural dyes in extracts from wool and silk fibres from archeological textiles. The examined objects originate from 4th to 12th Century Egypt and belong to the collection of Early Christian Art of the National Museum in Warsaw. Extraction from fibres was carried out with HCl solution containing ethanol or with warm pyridine. As the main individual chemical components of natural dyes, anthraquinone, indigoid and flavonoid dyes including alizarin, purpurin, luteolin, apigenin, carminic acid, ellagic acid, gallic acid, laccaic acids A and B and indigotin were found. For pyridine extracts another mobile phase with an optimized gradient of organic modifier concentration was used. With such an eluent the appearance of double peaks for indigotin and indirubin was eliminated. For acidic extraction of dyes from fibres, ethanol was used. Due to its higher boiling point than methanol it evaporates slower from the extraction solution enabling a more efficient extraction of dyes. PMID:12650256

  18. FRET Sensor for Erythrosine Dye Based on Organic Nanoparticles: Application to Analysis of Food Stuff.

    PubMed

    Mahajan, Prasad G; Bhopate, Dhanaji P; Kolekar, Govind B; Patil, Shivajirao R

    2016-07-01

    An aqueous suspension of fluorescent nanoparticles (PHNNPs) of naphthol based fluorescent organic compound 1-[(Z)-(2-phenylhydrazinylidene) methyl] naphthalene -2-ol (PHN) were prepared using reprecipitation method shows bathochromically shifted aggregation induced enhanced emission (AIEE) in the spectral region where erythrosine (ETS) food dye absorbs strongly. The average size of 72.6 nm of aqueous suspension of PHNNPs obtained by Dynamic light scattering results shows a narrow particle size distribution. The negative zeta potential of nano probe (-22.6 mV) responsible to adsorb oppositely charged analyte on its surface and further permit to bind nano probe and analyte within the close distance proximity required for efficient fluorescence resonance energy transfer (FRET) to take place from donor (PHNNPs) to acceptor (ETS). Systematic FRET experiments performed by measuring fluorescence quenching of PHNNPs with successive addition of ETS solution exploited the use of the PHNNPs as a novel nano probe for the detection of ETS in aqueous solution with extremely lower limit of detection equal to 3.6 nM (3.1 ng/mL). The estimation of photo kinetic and thermodynamic parameters such as quenching rate constant, enthalpy change (∆H), Gibbs free energy change (∆G) and entropy change (∆S) was obtained by the quenching results obtained at different constant temperatures which were found to fit the well-known Stern-Volmer relation. The mechanism of binding and fluorescence quenching of PHNNPs by ETS food dye is proposed on the basis of results obtained in photophysical studies, thermodynamic parameter, energy transfer efficiency, critical energy transfer distance (R0) and distance of approach between donor-acceptor molecules (r). The proposed FRET method based on fluorescence quenching of PHNNPs was successfully applied to develop an analytical method for estimation of ETS from food stuffs without interference of other complex ingredients. Graphical Abstract A

  19. FRET Sensor for Erythrosine Dye Based on Organic Nanoparticles: Application to Analysis of Food Stuff.

    PubMed

    Mahajan, Prasad G; Bhopate, Dhanaji P; Kolekar, Govind B; Patil, Shivajirao R

    2016-07-01

    An aqueous suspension of fluorescent nanoparticles (PHNNPs) of naphthol based fluorescent organic compound 1-[(Z)-(2-phenylhydrazinylidene) methyl] naphthalene -2-ol (PHN) were prepared using reprecipitation method shows bathochromically shifted aggregation induced enhanced emission (AIEE) in the spectral region where erythrosine (ETS) food dye absorbs strongly. The average size of 72.6 nm of aqueous suspension of PHNNPs obtained by Dynamic light scattering results shows a narrow particle size distribution. The negative zeta potential of nano probe (-22.6 mV) responsible to adsorb oppositely charged analyte on its surface and further permit to bind nano probe and analyte within the close distance proximity required for efficient fluorescence resonance energy transfer (FRET) to take place from donor (PHNNPs) to acceptor (ETS). Systematic FRET experiments performed by measuring fluorescence quenching of PHNNPs with successive addition of ETS solution exploited the use of the PHNNPs as a novel nano probe for the detection of ETS in aqueous solution with extremely lower limit of detection equal to 3.6 nM (3.1 ng/mL). The estimation of photo kinetic and thermodynamic parameters such as quenching rate constant, enthalpy change (∆H), Gibbs free energy change (∆G) and entropy change (∆S) was obtained by the quenching results obtained at different constant temperatures which were found to fit the well-known Stern-Volmer relation. The mechanism of binding and fluorescence quenching of PHNNPs by ETS food dye is proposed on the basis of results obtained in photophysical studies, thermodynamic parameter, energy transfer efficiency, critical energy transfer distance (R0) and distance of approach between donor-acceptor molecules (r). The proposed FRET method based on fluorescence quenching of PHNNPs was successfully applied to develop an analytical method for estimation of ETS from food stuffs without interference of other complex ingredients. Graphical Abstract A

  20. Efficient adsorbents of nanoporous aluminosilicate monoliths for organic dyes from aqueous solution.

    PubMed

    El-Safty, Sherif A; Shahat, Ahmed; Awual, Md Rabiul

    2011-07-01

    Growing public awareness on the potential risk to humans of toxic chemicals in the environment has generated demand for new and improved methods for toxicity assessment and removal, rational means for health risk estimation. With the aim of controlling nanoscale adsorbents for functionality in molecular sieving of organic pollutants, we fabricated cubic Im3m mesocages with uniform entrance and large cavity pores of aluminosilicates as highly promising candidates for the colorimetric monitoring of organic dyes in an aqueous solution. However, a feasible control over engineering of three-dimensional (3D) mesopore cage structures with uniform entrance (~5 nm) and large cavity (~10 nm) allowed the development of nanoadsorbent membranes as a powerful tool for large-quantity and high-speed (in minutes) adsorption/removal of bulk molecules such as organic dyes. Incorporation of high aluminum contents (Si/Al=1) into 3D cubic Im3m cage mesoporous silica monoliths resulted in small, easy-to-use optical adsorbent strips. In such adsorption systems, natural surfaces of active acid sites of aluminosilicate strips strongly induced both physical adsorption of chemically responsive dyes and intraparticle diffusion into cubic Im3m mesocage monoliths. Results likewise indicated that although aluminosilicate strips with low Si/Al ratios exhibit distortion in pore ordering and decrease in surface area and pore volume, enhancement of both molecular converges and intraparticle diffusion onto the network surfaces and into the pore architectures of adsorbent membranes was achieved. Moreover, 3D mesopore cage adsorbents are reversible, offering potential for multiple adsorption assays.

  1. Assessment of the ΔSCF density functional theory approach for electronic excitations in organic dyes

    SciTech Connect

    Kowalczyk, T.; Yost, S. R.; Van Voorhis, T.

    2010-01-01

    This paper assesses the accuracy of the ΔSCF method for computing low-lying HOMO→LUMO transitions in organic dye molecules. For a test set of vertical excitation energies of 16 chromophores, surprisingly similar accuracy is observed for time-dependent density functional theory and for ΔSCF density functional theory. In light of this performance, we reconsider the ad hoc ΔSCF prescription and demonstrate that it formally obtains the exact stationary density within the adiabatic approximation, partially justifying its use. The relative merits and future prospects of ΔSCF for simulating individual excited states are discussed.

  2. Third order optical nonlinearities characteristics of Disperse Red1 organic dye molecules inside of polymeric nanocapsules

    NASA Astrophysics Data System (ADS)

    Sharifimehr, Mohammad Reza; Ayoubi, Kazem; Mohajerani, Ezeddin

    2015-11-01

    Measuring nonlinear optical response of a specific material in a mixture, not only leads to investigate the behavior of a particular component in various circumstances, but also can be a way to select suitable combination and optimum concentration of additives and therefore obtaining the maximum nonlinear optical signals. In this work, by using dual-arm Z-scan technique, the nonlinear refractive index of Disperse Red1 (DR1) organic dye molecules inside the core of prepared polymeric nanocapsules was measured among various materials which prepared nanocapsules were made of them. Then the measured value was compared with nonlinear refractive index of DR1 solved in dichloromethane.

  3. Effect of viscosity, basicity and organic content of composite flocculant on the decolorization performance and mechanism for reactive dyeing wastewater.

    PubMed

    Wang, Yuanfang; Gao, Baoyu; Yue, Qinyan; Wang, Yan

    2011-01-01

    A coagulation/flocculation process using the composite flocculant polyaluminum chloride-epichlorohydrin dimethylamine (PAC-EPI-DMA) was employed for the treatment of an anionic azo dye (Reactive Brilliant Red K-2BP dye). The effect of viscosity (eta), basicity (B = [OH]/[Al]) and organic content (W(P)) on the flocculation performance as well as the mechanism of PAC-EPI-DMA flocculant were investigated. The eta was the key factor affecting the dye removal efficiency of PAC-EPI-DMA. PAC-EPI-DMA with an intermediate eta (2400 mPa x sec) gave higher decolorization efficiency by adsorption bridging and charge neutralization due to the co-effect of PAC and EPI-DMA polymers. The W(P) of the composite flocculant was a minor important factor for the flocculation. The adsorption bridging of PAC-EPI-DMA with eta of 300 or 4300 mPa x sec played an important role with the increase of W(P), whereas the charge neutralization of them was weaker with the increase of W(P). There was interaction between W(P) and B on the removal of reactive dye. The composite flocculant with intermediate viscosity and organic content was effective for the treatment of reactive dyeing wastewater, which could achieve high reactive dye removal efficiency with low organic dosage. PMID:22432257

  4. Post-assembly atomic layer deposition of ultrathin metal-oxide coatings enhances the performance of an organic dye-sensitized solar cell by suppressing dye aggregation.

    PubMed

    Son, Ho-Jin; Kim, Chul Hoon; Kim, Dong Wook; Jeong, Nak Cheon; Prasittichai, Chaiya; Luo, Langli; Wu, Jinsong; Farha, Omar K; Wasielewski, Michael R; Hupp, Joseph T

    2015-03-11

    Dye aggregation and concomitant reduction of dye excited-state lifetimes and electron-injection yields constitute a significant mechanism for diminution of light-to-electrical energy conversion efficiencies in many dye-sensitized solar cells (DSCs). For TiO2-based DSCs prepared with an archetypal donor-acceptor organic dye, (E)-2-cyano-3-(5'-(5''-(p-(diphenylamino)phenyl)-thiophen-2''-yl)thiophen-2'-yl)acrylic acid (OrgD), we find, in part via ultrafast spectroscopy measurements, that postdye-adsorption atomic layer deposition (ALD) of ultrathin layers of either TiO2 or Al2O3 effectively reverses residual aggregation. Notably, the ALD treatment is significantly more effective than the widely used aggregation-inhibiting coadsorbent, chenodeoxycholic acid. Primarily because of reversal of OrgD aggregation, and resulting improved injection yields, ALD post-treatment engenders a 30+% increase in overall energy conversion efficiency. A secondary contributor to increased currents and efficiencies is an ALD-induced attenuation of the rate of interception of injected electrons, resulting in slightly more efficient charge collection.

  5. 6H-Indolo[2,3-b]quinoxaline-based organic dyes containing different electron-rich conjugated linkers for highly efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Qian, Xing; Gao, Huan-Huan; Zhu, Yi-Zhou; Lu, Lin; Zheng, Jian-Yu

    2015-04-01

    A new class of organic dyes based on 6H-indolo[2,3-b]quinoxaline are synthesized and applied as photosensitizers for dye-sensitized solar cells. Different electron-rich π-conjugated bridges such as oligothiophene, thienyl carbazole, and furyl carbazole are introduced to cooperate with 6H-indolo[2,3-b]quinoxaline and cyanoacrylic acid anchoring group to give the dyes JY01, JY02, and JY03, respectively. Their photophysical, electrochemical, and photovoltaic properties are further investigated. All three dyes show good performances as photosensitizers. In particular, DSSC based on JY01 shows the best photovoltaic performance with a short-circuit photocurrent density of 16.0 mA cm-2, an open-circuit photovoltage of 708 mV and a fill factor of 0.67, corresponding to an overall power conversion efficiency of 7.62% under AM 1.5 irradiation (100 mW cm-2).

  6. Indolo[3,2-b]carbazole-based multi-donor-π-acceptor type organic dyes for highly efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Qian, Xing; Shao, Li; Li, Hongmei; Yan, Rucai; Wang, Xiaoying; Hou, Linxi

    2016-07-01

    Four novel indolo[3,2-b]carbazole-based multi-donor-π-acceptor type organic dyes QX01-04 have been designed, synthesized, and applied for dye-sensitized solar cells. These dyes consist of an indolo[3,2-b]carbazole core acting as the main donor group, a couple of groups such as ethylbenzene, N,N-diethylaniline, ethyloxylbenzene, and octyloxylbenzene acting as the secondary donors. The photophysical, electrochemical, and theoretical studies indicate that the four dyes are all capable as the photosensitizers. When introducing N,N-diethylaniline as the secondary donor, QX02 exhibits a broader absorption region and significantly improved IPCE values, which ensured a good light-harvesting ability and a high Jsc of 15.2 mA cm-2. Finally, QX02-based cell achieved a high efficiency of 8.09% which is very close to that of the commercial N719-based cell (8.26%) under 100 mW cm-2 irradiation.

  7. A Research Module for the Organic Chemistry Laboratory: Multistep Synthesis of a Fluorous Dye Molecule.

    PubMed

    Slade, Michael C; Raker, Jeffrey R; Kobilka, Brandon; Pohl, Nicola L B

    2014-01-14

    A multi-session research-like module has been developed for use in the undergraduate organic teaching laboratory curriculum. Students are tasked with planning and executing the synthesis of a novel fluorous dye molecule and using it to explore a fluorous affinity chromatography separation technique, which is the first implementation of this technique in a teaching laboratory. Key elements of the project include gradually introducing students to the use of the chemical literature to facilitate their searching, as well as deliberate constraints designed to force them to think critically about reaction design and optimization in organic chemistry. The project also introduces students to some advanced laboratory practices such as Schlenk techniques, degassing of reaction mixtures, affinity chromatography, and microwave-assisted chemistry. This provides students a teaching laboratory experience that closely mirrors authentic synthetic organic chemistry practice in laboratories throughout the world.

  8. A Research Module for the Organic Chemistry Laboratory: Multistep Synthesis of a Fluorous Dye Molecule

    PubMed Central

    2014-01-01

    A multi-session research-like module has been developed for use in the undergraduate organic teaching laboratory curriculum. Students are tasked with planning and executing the synthesis of a novel fluorous dye molecule and using it to explore a fluorous affinity chromatography separation technique, which is the first implementation of this technique in a teaching laboratory. Key elements of the project include gradually introducing students to the use of the chemical literature to facilitate their searching, as well as deliberate constraints designed to force them to think critically about reaction design and optimization in organic chemistry. The project also introduces students to some advanced laboratory practices such as Schlenk techniques, degassing of reaction mixtures, affinity chromatography, and microwave-assisted chemistry. This provides students a teaching laboratory experience that closely mirrors authentic synthetic organic chemistry practice in laboratories throughout the world. PMID:24501431

  9. Development of a rapid and simple method for detection of protein contaminants in carmine.

    PubMed

    Nakayama, Norihisa; Ohtsu, Yutaka; Maezawa-Kase, Daisuke; Sano, Ken-Ichi

    2015-01-01

    Protein contaminants in carmine can cause dyspnea and anaphylactic reactions in users and consumers of products containing this pigment. The method generally used for detection of proteins in carmine has low reproducibility and is time-consuming. In this study, a rapid, simple, and highly reproducible method was developed for the detection of protein contaminants in carmine. This method incorporates acidic protein denaturation conditions and ultrafiltration. To prevent protein aggregation, sodium dodecyl sulfate containing gel electrophoresis running buffer was used for dispersing the carmine before filtration. An ultrafiltration device was used to separate the protein contaminants from carminic acid in the carmine solution. Two ultrafiltration devices were compared, and a cylindrical device containing a modified polyethersulfone membrane gave the best results. The method had high reproducibility. PMID:25892994

  10. Development of a Rapid and Simple Method for Detection of Protein Contaminants in Carmine

    PubMed Central

    Nakayama, Norihisa; Ohtsu, Yutaka; Maezawa-Kase, Daisuke; Sano, Ken-Ichi

    2015-01-01

    Protein contaminants in carmine can cause dyspnea and anaphylactic reactions in users and consumers of products containing this pigment. The method generally used for detection of proteins in carmine has low reproducibility and is time-consuming. In this study, a rapid, simple, and highly reproducible method was developed for the detection of protein contaminants in carmine. This method incorporates acidic protein denaturation conditions and ultrafiltration. To prevent protein aggregation, sodium dodecyl sulfate containing gel electrophoresis running buffer was used for dispersing the carmine before filtration. An ultrafiltration device was used to separate the protein contaminants from carminic acid in the carmine solution. Two ultrafiltration devices were compared, and a cylindrical device containing a modified polyethersulfone membrane gave the best results. The method had high reproducibility. PMID:25892994

  11. Hierarchical assembly of metal nanoparticles, quantum dots and organic dyes using DNA origami scaffolds

    NASA Astrophysics Data System (ADS)

    Schreiber, Robert; Do, Jaekwon; Roller, Eva-Maria; Zhang, Tao; Schüller, Verena J.; Nickels, Philipp C.; Feldmann, Jochen; Liedl, Tim

    2014-01-01

    The self-assembly of nanoscale elements into three-dimensional structures with precise shapes and sizes is important in fields such as nanophotonics, metamaterials and biotechnology. Short molecular linkers have previously been used to create assemblies of nanoparticles, but the approach is limited to small interparticle distances, typically less than 10 nm. Alternatively, DNA origami can precisely organize nanoscale objects over much larger length scales. Here we show that rigid DNA origami scaffolds can be used to assemble metal nanoparticles, quantum dots and organic dyes into hierarchical nanoclusters that have a planet-satellite-type structure. The nanoclusters have a tunable stoichiometry, defined distances of 5-200 nm between components, and controllable overall sizes of up to 500 nm. We also show that the nanoscale components can be positioned along the radial DNA spacers of the nanostructures, which allows short- and long-range interactions between nanoparticles and dyes to be studied in solution. The approach could, in the future, be used to construct efficient energy funnels, complex plasmonic architectures, and porous, nanoengineered scaffolds for catalysis.

  12. Preparation of C60 Nanowhiskers-SnO2 Nanocomposites and Photocatalytic Degradation of Organic Dyes.

    PubMed

    Park, Hae Soo; Ko, Weon Bae

    2015-10-01

    C60 nanowhiskers were prepared using a liquid-liquid interfacial precipitation (LLIP) method. Tin oxide (SnO2) nanoparticles were synthesized by a reaction of tin (IV) chloride pentahydrate with ammonium nitrate in an electric furnace. The C60 nanowhiskers-SnO2 nanocomposites were calcined in an electric furnace at 700 °C under an inert argon gas atmosphere for 2 h. The crystallinity, morphology and optical properties of the samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and UV-vis spectrophotometry. The photocatalytic activity of the C60 nanowhiskers-SnO2 nanocomposites in the degradation of the organic dyes, such as methylene blue, methyl orange, rhodamine B, and brilliant green, under ultraviolet light at 254 nm by UV-vis spectrophotometry was evaluated and compared with that of C60 nanowhiskers and SnO2 nanoparticles. The experimental results showed that C60 nanowhiskers-SnO2 nanocomposites exhibited remarkably higher photocatalytic degradation of organic dyes compared to C60 nanowhiskers and SnO2 nanoparticles.

  13. Preparation of ZnS-graphene nanocomposites under electric furnace and photocatalytic degradation of organic dyes.

    PubMed

    Park, Hae Soo; Ko, Weon Bae

    2014-11-01

    Zinc sulfide (ZnS) nanoparticles were synthesized from zinc nitrate hexahydrate and thiourea under microwave irradiation. The ZnS-graphene nanocomposites were calcined in an electric furnace at 700 degrees C under an inert argon gas atmosphere for 2 hr. The heated ZnS-graphene nanocomposites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV-vis spectrophotometry. After heat treatment, ZnS-graphene nanocomposites had a more porous and larger surface area, than the unheated ZnS-graphene nanocomposites. The photocatalytic activity of the heated ZnS-graphene nanocomposites in the degradation of organic dyes, such as methylene blue, methyl orange, and rhodamine B, under ultraviolet light at 254 nm by UV- vis spectrophotometer was evaluated and compared with that of the unheated ZnS nanoparticles, heated ZnS nanoparticles, unheated ZnS-graphene nanocomposites. Among the our experimental results as a photocatalyst, the heated ZnS-graphene nanocomposites exhibited remarkably higher photocatalytic degradation of organic dyes as compared to other nanomaterials such as unheated ZnS nanoparticles and heated ZnS-graphene nanocomposites.

  14. Preparation of ZnS-graphene nanocomposites under electric furnace and photocatalytic degradation of organic dyes.

    PubMed

    Park, Hae Soo; Ko, Weon Bae

    2014-11-01

    Zinc sulfide (ZnS) nanoparticles were synthesized from zinc nitrate hexahydrate and thiourea under microwave irradiation. The ZnS-graphene nanocomposites were calcined in an electric furnace at 700 degrees C under an inert argon gas atmosphere for 2 hr. The heated ZnS-graphene nanocomposites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV-vis spectrophotometry. After heat treatment, ZnS-graphene nanocomposites had a more porous and larger surface area, than the unheated ZnS-graphene nanocomposites. The photocatalytic activity of the heated ZnS-graphene nanocomposites in the degradation of organic dyes, such as methylene blue, methyl orange, and rhodamine B, under ultraviolet light at 254 nm by UV- vis spectrophotometer was evaluated and compared with that of the unheated ZnS nanoparticles, heated ZnS nanoparticles, unheated ZnS-graphene nanocomposites. Among the our experimental results as a photocatalyst, the heated ZnS-graphene nanocomposites exhibited remarkably higher photocatalytic degradation of organic dyes as compared to other nanomaterials such as unheated ZnS nanoparticles and heated ZnS-graphene nanocomposites. PMID:25958578

  15. Sol-gel-derived silica films with tailored microstructures for applications requiring organic dyes

    SciTech Connect

    Logan, M.N.; Prabakar, S.; Brinker, C.J. |

    1994-09-01

    A three-step sol-gel process was developed to prepare organic dye-doped thin films with tailored porosity for applications in chemical sensing and optoelectronics. Varying the acid- and base-catalyzed hydrolysis steps of sols prepared from tetraethoxysilane with identical final H{sub 2}O/Si ratios, dilution factors and pH resulted in considerably different distributions of the silicate polymers in the sol (determined by {sup 29}Si NMR) and considerably different structures for the polymer clusters (determined by SAXS). During film formation these kinetic effects cause differences in the packing and collapse of the silicate network, leading to thin films with different refractive indices and volume fraction porosities. Under conditions where small pore-plugging species were avoided, the porosities of as-deposited films could be varied by aging the sol prior to film deposition. This strategy, which relies on the growth and aggregation of fractal polymeric clusters, is compatible with the low temperature and near neutral pH requirements of organic dyes.

  16. Preparation of C60 Nanowhiskers-SnO2 Nanocomposites and Photocatalytic Degradation of Organic Dyes.

    PubMed

    Park, Hae Soo; Ko, Weon Bae

    2015-10-01

    C60 nanowhiskers were prepared using a liquid-liquid interfacial precipitation (LLIP) method. Tin oxide (SnO2) nanoparticles were synthesized by a reaction of tin (IV) chloride pentahydrate with ammonium nitrate in an electric furnace. The C60 nanowhiskers-SnO2 nanocomposites were calcined in an electric furnace at 700 °C under an inert argon gas atmosphere for 2 h. The crystallinity, morphology and optical properties of the samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and UV-vis spectrophotometry. The photocatalytic activity of the C60 nanowhiskers-SnO2 nanocomposites in the degradation of the organic dyes, such as methylene blue, methyl orange, rhodamine B, and brilliant green, under ultraviolet light at 254 nm by UV-vis spectrophotometry was evaluated and compared with that of C60 nanowhiskers and SnO2 nanoparticles. The experimental results showed that C60 nanowhiskers-SnO2 nanocomposites exhibited remarkably higher photocatalytic degradation of organic dyes compared to C60 nanowhiskers and SnO2 nanoparticles. PMID:26726474

  17. Switch-On Fluorescence of a Perylene-Dye-Functionalized Metal-Organic Framework through Postsynthetic Modification.

    PubMed

    Dietl, Christian; Hintz, Henrik; Rühle, Bastian; Schmedt Auf der Günne, Jörn; Langhals, Heinz; Wuttke, Stefan

    2015-07-20

    A perylene dye was introduced directly as a linker into a metal-organic framework (MOF) during synthesis. Depending on the dye concentration in the MOF synthesis mixture, different fluorescent materials were generated. The successful incorporation of the dye was proven by using (13) C and (27) Al MAS NMR spectroscopy, by solution NMR spectroscopy after digestion of the MOF sample, and by synthesizing a reference dye without connecting groups, which could coordinate on the metal-oxo cluster inside the MOF. Fluorescence quenching effects of the MOF linker, 2-aminoterephthalate, were observed and overcome by postsynthetic modification with acetic anhydride. We show here for the first time that amino groups, which can be used as anchoring points for covalent attachment of other molecules, are responsible for fluorescence quenching. Thus, a very promising strategy to implement switchable fluorescence into MOFs is shown here.

  18. Comparative studies on rigid π linker-based organic dyes: structure-property relationships and photovoltaic performance.

    PubMed

    Li, Hairong; Koh, Teck Ming; Hao, Yan; Zhou, Feng; Abe, Yuichiro; Su, Haibin; Hagfeldt, Anders; Grimsdale, Andrew C

    2014-12-01

    A series of six structurally correlated donor-π bridge-acceptor organic dyes were designed, synthesized, and applied as sensitizers in dye-sensitized solar cells. Using the most widely studied donor (triarylamine) and cyclopenta[1,2-b:5,4-b']dithiophene or cyclopenta[1,2-b:5,4-b']dithiophene[2',1':4,5]thieno[2,3-d]thiophene as π spacers, their structure-property relationships were investigated in depth by photophysical techniques and theoretical calculations. It was found that the photovoltaic performance of these dyes largely depends on their electronic structures, which requires synergistic interaction between donors and acceptors. Increasing the electron richness of the donor or the elongation of π-conjugated bridges does not necessarily lead to higher performance. Rather, it is essential to rationally design the dyes by balancing their light-harvesting capability with achieving suitable energy levels to guarantee unimpeded charge separation and transport.

  19. Connecting Direct C-H Arylation Reactions with Dye-Sensitized Solar Cells: A Shortcut to D-A-π-A Organic Dyes.

    PubMed

    Lin, Po-Han; Lu, Te-Jui; Cai, Deng-Jhou; Lee, Kun-Mu; Liu, Ching-Yuan

    2015-10-12

    A step-economical synthetic strategy is developed to target thieno[3,4-c]pyrrole-4,6-dione (TPD)-based D-A-π-A organic dyes for dye-sensitized solar cells (DSSCs). Through sequential Pd-catalyzed direct C-H (hetero)arylation reaction, synthesis of the push-pull-type small molecules is reduced from the traditional six steps to two steps. In this report, we focus on the optimization of the key C-H monoarylation of TPD by screening ligands, acid additives, bases, and solvents. The reaction proves versatile toward new D-A-π-A organic dyes with a variety of different donor groups, and several derivatives are efficiently prepared under optimum reaction conditions. The sensitive aldehyde functionality that is a required intermediate for conversion into anchoring groups for TiO2 is well tolerated. Based on our synthetic study, DSSCs are fabricated and characterized using two designed sensitizers. The photovoltaic characterization of the devices affords an open-circuit voltage of 0.60-0.69 V, a short-circuit current density of 10.85-11.07 mA cm(-2), and a fill factor of 69.9-70.8 %, which corresponds to an overall power conversion efficiency of 4.61-5.33 %.

  20. Near infrared organic semiconducting materials for bulk heterojunction and dye-sensitized solar cells.

    PubMed

    Singh, Surya Prakash; Sharma, G D

    2014-06-01

    Dye sensitized solar cells (DSSCs) and bulk heterojunction (BHJ) solar cells have been the subject of intensive academic interest over the past two decades, and significant commercial effort has been directed towards this area with the vison of developing the next generation of low cost solar cells. Materials development has played a vital role in the dramatic improvement of both DSSC and BHJ solar cell performance in the recent years. Organic conjugated polymers and small molecules that absorb solar light in the visible and near infrared (NIR) regions represent a class of emering materials and show a great potential for the use of different optoelectronic devices such as DSSCs and BHJ solar cells. This account describes the emering class of near infrared (NIR) organic polymers and small molecules having donor and acceptors units, and explores their potential applications in the DSSCs and BHJ solar cells.

  1. First principles study of thieno[2,3-b]indole-based organic dyes for dye-sensitized solar cells: Screen novel π-linkers and explore the interface between photosensitizers and TiO2

    NASA Astrophysics Data System (ADS)

    Wen, Yaping; Wu, Wenpeng; Li, Yuanyuan; Zhang, Weiyi; Zeng, Zhaoyang; Wang, Li; Zhang, Jinglai

    2016-09-01

    Four organic compounds with different π-linkers are theoretically explored as potential photosensitizers for application in dye-sensitized solar cells (DSSCs). Besides the isolated dyes, the interfacial properties of dyes adsorbed on TiO2 anatase (101) surface are theoretically investigated. The overall conversion efficiency (η) of DSSCs is evaluated by the following items on the basis of the isolated dyes, including structures, absorption spectrum, energy gap, open-circuit voltage (Voc), short-circuit current density (Jsc), and reorganization energies (λtotal). After adsorbed on the TiO2 surface, the electron would be efficiently injected from dye into the TiO2 surface because of the increased of the lowest unoccupied molecular orbital (LUMO) energy level of the dyes, the decreased of the conduction band of TiO2 surface, and the narrowed band gaps for both dye and TiO2. Moreover, the injection times are in a reasonable range indicating that they are ideal dyes. Combination of all items, the performance of THI-2T-C (See Scheme 1, the sketch structures of all the investigated isolated dyes) stands out from the rest investigated dyes from the theoretical viewpoint. Only enlargement of the π-linker extent is not a smart choice, since the nature of π-linker plays a more important role in affecting the performance of DSSCs.

  2. Detailed analysis of ultrathin fluorescent red dye interlayer for organic photovoltaic cells

    NASA Astrophysics Data System (ADS)

    Zang, Yue; Yu, Jun-Sheng; Wang, Na-Na; Jiang, Ya-Dong

    2011-01-01

    The influence of an ultrathin 4-(dicyanomethylene)-2-t-butyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJTB) fluorescent dye layer at donor/acceptor heterojunction on the performance of small-molecule organic photovoltaic (OPV) cell is studied. The structure of OPV cell is of indium-tin oxide (ITO)/copper phthalocyanine (CuPc)/DCJTB/fullerene (C60)/bathophenanthroline (Bphen)/Ag. The results show that open circuit voltage (VOC) increases to 0.57 V as the film thickness of DCJTB layer increases from 0.2 to 2.0 nm. By using an equivalent circuit model, the enhancement of VOC is found to be attributed to the reduced reverse saturation current density (JS) which is due to the lower highest occupied molecular orbital (HOMO) level in DCJTB than that in CuPc. Also, the short circuit current density (JSC) is affected when the DCJTB layer becomes thicker, resulting from the high series resistance RSA due to the low charge carrier mobility of fluorescent red dye.

  3. Visible light assisted degradation of organic dye using Ag{sub 3}PO{sub 4}

    SciTech Connect

    Dhanabal, R.; Bose, A. Chandra; Velmathi, S.

    2015-06-24

    The study of visible light photodegradation of organic dye Methylene Blue (MB) have been investigated using silver phosphate (Ag{sub 3}PO{sub 4}) as a photocatalyst which is good efficient material for photocatalytic reaction. The simple ion-exchange method is used to prepare Ag{sub 3}PO{sub 4}. The structure of the material have been confirmed using X-ray diffraction which shows cubic structure of Ag{sub 3}PO{sub 4}. The functional group of the Ag{sub 3}PO{sub 4} has been verified by Fourier transform infrared spectroscopy. The bandgap of Ag{sub 3}PO{sub 4} is calculated using kubelka-munk function from the ultra violet-visible diffuse reflectance spectroscopy, the absorption of Ag{sub 3}PO{sub 4} starts from 470 nm. Under simulated visible light irradiation, Ag{sub 3}PO{sub 4} catalyst exhibits good catalytic ability for degrading MB dye.

  4. A novel porous anionic metal-organic framework with pillared double-layer structure for selective adsorption of dyes

    NASA Astrophysics Data System (ADS)

    Sheng, Shu-Nan; Han, Yi; Wang, Bin; Zhao, Cui; Yang, Fan; Zhao, Min-Jian; Xie, Ya-Bo; Li, Jian-Rong

    2016-01-01

    A novel porous anionic metal-organic framework, (Me2NH2)2[Zn2L1.5bpy]·2DMF (BUT-201; H4L=4,8-disulfonaphthalene-2,6-dicarboxylic acid; bpy=4,4-bipyridine; DMF=N,N-dimethylformamide), with pillared double-layer structure has been synthesized through the reaction of a sulfonated carboxylic acid ligand and Zn(NO3)2·6H2O with 4,4-bipyridine as a co-ligand. It is found that BUT-201 can rapidly adsorb cationic dyes with a smaller size such as Methylene Blue (MB) and Acriflavine Hydrochloride (AH) by substitution of guest (CH3)2NH2+, but has no adsorption towards the cationic dyes with a lager size such as Methylene Violet (MV), the anionic dyes like C. I. Acid Yellow 1 (AY1) and neutral dyes like C. I. Solvent Yellow 7 (SY7), respectively. The results show that the adsorption behavior of BUT-201 relates not only to the charge but also to the size/shape of dyes. Furthermore, the adsorbed dyes can be gradually released in the methanol solution of LiNO3.

  5. A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes.

    PubMed

    Chen, Di-ming; Shi, Wei; Cheng, Peng

    2015-01-01

    A cage-based cationic body-centered metal-organic framework was successfully synthesized using a custom-designed bifunctional triazolcarboxylate ligand. It shows interesting single-crystal-to-single-crystal transformation upon solvent exchange process and selective uptake of organic dyes.

  6. Thermal diffusivity measurements of sub-micron organic dye thin films using a high temperature superconductor bolometer

    NASA Astrophysics Data System (ADS)

    Savoy, Steven M.; Wells, Cyndi A.; McDevitt, John T.; Rhodes, Timothy A.

    1998-12-01

    The thermal diffusivity of a thin organic dye layer deposited atop thin films of the high temperature superconductor YBa2Cu3O7-δ is measured using a pulsed laser flash method. Here, the underlying superconductor acts as a highly sensitive temperature transducer after appropriate conversion of the transient voltage response from 7 ns optical pulses. Film surface temperature decays for several thicknesses of the dye layers were evaluated; these decays exhibited a linear dependence of the time at half temperature maximum versus thickness squared. Three dimensional finite difference modeling was used to study and extract the thermal diffusivity values of the thin organic layers as well as to investigate the transient temperature distributions within the dye and superconductor areas.

  7. Molecular engineering of organic dyes with a hole-extending donor tail for efficient all-solid-state dye-sensitized solar cells.

    PubMed

    Lu, Jianfeng; Chang, Yu-Cheng; Cheng, Hsu-Yang; Wu, Hui-Ping; Cheng, Yibing; Wang, Mingkui; Diau, Eric Wei-Guang

    2015-08-10

    We report a new concept for the design of metal-free organic dyes (OD5-OD9) with an extended donor-π-acceptor (D-π-A) molecular framework, in which the donor terminal unit is attached by a hole-extending side chain to retard back electron transfer and charge recombination; the π-bridge component contains varied thiophene-based substituents to enhance the light-harvesting ability of the device. The best dye (OD9) has a D-A-π-A configuration with the hexyloxyphenylthiophene (HPT) side chain as a hole-extension component and a benzothiadiazole (BTD) internal acceptor as a π-extension component. The co-sensitization of OD9 with the new porphyrin dye LW24 enhanced the light-harvesting ability to 800 nm; thus, a power conversion efficiency 5.5 % was achieved. Photoinduced absorption (PIA) and transient absorption spectral (TAS) techniques were applied to account for the observed trend of the open-circuit voltage (VOC ) of the devices. This work provides insights into the molecular design, photovoltaic performance, and kinetics of charge recombination. PMID:26119886

  8. Use of grape seed and its natural polyphenol extracts as a natural organic coagulant for removal of cationic dyes.

    PubMed

    Jeon, Jong-Rok; Kim, Eun-Ju; Kim, Young-Mo; Murugesan, Kumarasamy; Kim, Jae-Hwan; Chang, Yoon-Seok

    2009-11-01

    Natural organic coagulants (NOCs) such as chitosan and Moringa oleifera seeds have been extensively characterized for potential application in water treatment as an alternative to metal-based coagulants. However, the action of both chitosan and M. oleifera seeds is mainly restricted to anionic organic pollutants because of their cationic functional groups affording poor cationic pollutant coagulation by electrostatic repulsion. In this study, we employed ethanolic grape seed extract (GSE) and grape seed-derived polyphenols such as tannic acid and catechin in an effort to find novel NOCs showing stable anionic forms for removal of cationic organic pollutants. The target substances tested were malachite green (MG) and crystal violet (CV), both mutagenic cationic dyes. Polyphenol treatment induced fast decolorization followed by gradual floc formation concomitant with red or blue shifts in maximum absorbance wavelengths of the cationic dyes. Liquid chromatography analysis of flocs formed by polyphenols directly showed that initial supramolecular complexes attributed mainly to electrostatic attraction between polyphenol hydroxyphenyl groups and cationic dyes further progressed into stronger aggregates, leading to precipitation of dye-polyphenol complexes. Consistent with the results obtained using catechin and tannic acid, use of GSE also resulted in effective decolorization and coagulation of soluble MG and CV in aqueous solutions. Screening of several organic GSE components for NOC activity strongly suggested that natural polyphenols are the main organic ingredients causing MG and CV removal via gradual floc formation. The treatment by natural polyphenols and GSE decreased toxicity of MG- or CV-contaminated water.

  9. A novel structural Fenton-like nanocatalyst with highly improved catalytic performance for generalized preparation of iron oxide@organic dye polymer core-shell nanospheres.

    PubMed

    Zhao, Guanghui; Peng, Xiaomen; Li, Hongping; Wang, Jianzhi; Zhou, Lincheng; Zhao, Tianqi; Huang, Zhihao; Jiang, Haifei

    2015-05-01

    FexOy@FexOy/C nanoparticles with a soap-bubble-like shell have been synthesized, and the materials exhibit excellent Fenton catalytic performance. More importantly, FexOy@FexOy/C nanoparticles as catalysts and precursors could catalyze organic dye molecules to form iron oxide@organic dye polymer core-shell nanospheres.

  10. A novel structural Fenton-like nanocatalyst with highly improved catalytic performance for generalized preparation of iron oxide@organic dye polymer core-shell nanospheres.

    PubMed

    Zhao, Guanghui; Peng, Xiaomen; Li, Hongping; Wang, Jianzhi; Zhou, Lincheng; Zhao, Tianqi; Huang, Zhihao; Jiang, Haifei

    2015-05-01

    FexOy@FexOy/C nanoparticles with a soap-bubble-like shell have been synthesized, and the materials exhibit excellent Fenton catalytic performance. More importantly, FexOy@FexOy/C nanoparticles as catalysts and precursors could catalyze organic dye molecules to form iron oxide@organic dye polymer core-shell nanospheres. PMID:25828271

  11. The Rise of Near-Infrared Emitters: Organic Dyes, Porphyrinoids, and Transition Metal Complexes.

    PubMed

    Barbieri, Andrea; Bandini, Elisa; Monti, Filippo; Praveen, Vakayil K; Armaroli, Nicola

    2016-08-01

    In recent years, the interest in near-infrared (NIR) emitting molecules and materials has increased significantly, thanks to the expansion of the potential technological applications of NIR luminescence in several areas such as bioimaging, sensors, telecommunications, and night-vision displays. This progress has been facilitated by the development of new synthetic routes for the targeted functionalization and expansion of established molecular frameworks and by the availability of simpler and cheaper NIR detectors. Herein, we present recent developments on three major classes of systems-i.e., organic dyes, porphyrinoids, and transition metal complexes-exhibiting the maximum of the emission band at λ > 700 nm. In particular, we focus on the design strategies that may increase the luminescence efficiency, while pushing the emission band more deeply in the NIR region. This overview suggests that further progress can be achieved in the near future, with enhanced availability of more robust, stronger, and cheaper NIR luminophores. PMID:27573399

  12. Hierarchically porous silicon-carbon-nitrogen hybrid materials towards highly efficient and selective adsorption of organic dyes

    NASA Astrophysics Data System (ADS)

    Meng, Lala; Zhang, Xiaofei; Tang, Yusheng; Su, Kehe; Kong, Jie

    2015-01-01

    The hierarchically macro/micro-porous silicon-carbon-nitrogen (Si-C-N) hybrid material was presented with novel functionalities of totally selective and highly efficient adsorption for organic dyes. The hybrid material was conveniently generated by the pyrolysis of commercial polysilazane precursors using polydivinylbenzene microspheres as sacrificial templates. Owing to the Van der Waals force between sp-hybridized carbon domains and triphenyl structure of dyes, and electrostatic interaction between dyes and Si-C-N matrix, it exhibites high adsorption capacity and good regeneration and recycling ability for the dyes with triphenyl structure, such as methyl blue (MB), acid fuchsin (AF), basic fuchsin and malachite green. The adsorption process is determined by both surface adsorption and intraparticle diffusion. According to the Langmuir model, the adsorption capacity is 1327.7 mg.g-1 and 1084.5 mg.g-1 for MB and AF, respectively, which is much higher than that of many other adsorbents. On the contrary, the hybrid materials do not adsorb the dyes with azo benzene structures, such as methyl orange, methyl red and congro red. Thus, the hierarchically porous Si-C-N hybrid material from a facile and low cost polymer-derived strategy provides a new perspective and possesses a significant potential in the treatment of wastewater with complex organic pollutants.

  13. Hierarchically porous silicon–carbon–nitrogen hybrid materials towards highly efficient and selective adsorption of organic dyes

    PubMed Central

    Meng, Lala; Zhang, Xiaofei; Tang, Yusheng; Su, Kehe; Kong, Jie

    2015-01-01

    The hierarchically macro/micro-porous silicon–carbon–nitrogen (Si–C–N) hybrid material was presented with novel functionalities of totally selective and highly efficient adsorption for organic dyes. The hybrid material was conveniently generated by the pyrolysis of commercial polysilazane precursors using polydivinylbenzene microspheres as sacrificial templates. Owing to the Van der Waals force between sp2-hybridized carbon domains and triphenyl structure of dyes, and electrostatic interaction between dyes and Si-C-N matrix, it exhibites high adsorption capacity and good regeneration and recycling ability for the dyes with triphenyl structure, such as methyl blue (MB), acid fuchsin (AF), basic fuchsin and malachite green. The adsorption process is determined by both surface adsorption and intraparticle diffusion. According to the Langmuir model, the adsorption capacity is 1327.7 mg·g−1 and 1084.5 mg·g−1 for MB and AF, respectively, which is much higher than that of many other adsorbents. On the contrary, the hybrid materials do not adsorb the dyes with azo benzene structures, such as methyl orange, methyl red and congro red. Thus, the hierarchically porous Si–C–N hybrid material from a facile and low cost polymer-derived strategy provides a new perspective and possesses a significant potential in the treatment of wastewater with complex organic pollutants. PMID:25604334

  14. Hierarchically porous silicon-carbon-nitrogen hybrid materials towards highly efficient and selective adsorption of organic dyes.

    PubMed

    Meng, Lala; Zhang, Xiaofei; Tang, Yusheng; Su, Kehe; Kong, Jie

    2015-01-01

    The hierarchically macro/micro-porous silicon-carbon-nitrogen (Si-C-N) hybrid material was presented with novel functionalities of totally selective and highly efficient adsorption for organic dyes. The hybrid material was conveniently generated by the pyrolysis of commercial polysilazane precursors using polydivinylbenzene microspheres as sacrificial templates. Owing to the Van der Waals force between sp-hybridized carbon domains and triphenyl structure of dyes, and electrostatic interaction between dyes and Si-C-N matrix, it exhibites high adsorption capacity and good regeneration and recycling ability for the dyes with triphenyl structure, such as methyl blue (MB), acid fuchsin (AF), basic fuchsin and malachite green. The adsorption process is determined by both surface adsorption and intraparticle diffusion. According to the Langmuir model, the adsorption capacity is 1327.7 mg·g(-1) and 1084.5 mg·g(-1) for MB and AF, respectively, which is much higher than that of many other adsorbents. On the contrary, the hybrid materials do not adsorb the dyes with azo benzene structures, such as methyl orange, methyl red and congro red. Thus, the hierarchically porous Si-C-N hybrid material from a facile and low cost polymer-derived strategy provides a new perspective and possesses a significant potential in the treatment of wastewater with complex organic pollutants. PMID:25604334

  15. Synthesis of magnetic nanoporous carbon from metal-organic framework for the fast removal of organic dye from aqueous solution

    NASA Astrophysics Data System (ADS)

    Jiao, Caina; Wang, Yanen; Li, Menghua; Wu, Qiuhua; Wang, Chun; Wang, Zhi

    2016-06-01

    In this paper, a magnetic nanoporous carbon (Fe3O4/NPC) was successfully synthesized by using MOF-5 as carbon precursor and Fe salt as magnetic precursor. The texture properties of the as-synthesized nanocomposite were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and N2 adsorption-desorption isotherms. The Fe3O4/NPC had a high surface area with strong magnetic strength. Its adsorption behavior was tested by its adsorption capacity for the removal of methylene blue from aqueous solution. The results demonstrated that the Fe3O4/NPC had a high adsorption capacity, rapid adsorption rate, and easy magnetic separabilty. Moreover, the adsorbent could be easily regenerated by washing it with ethanol. The Fe3O4/NPC can be used as a good alternative for the effective removal of organic dyes from wastewater.

  16. Screening for larvicidal activity of ten carminative plants.

    PubMed

    Pitasawat, B; Choochote, W; Kanjanapothi, D; Panthong, A; Jitpakdi, A; Chaithong, U

    1998-09-01

    Ten species of plants, reported to possess carminative property, were screened for larvicidal potential against Culex quinquefasciatus by exposing early 4th instar larvae to a series of concentrations of the ethanolic extracts of the plants. Mortality counts were made after 24 hours exposure. Probit analysis using computerized Harvard Programming (Hg1, 2) was employed to determine the LC50, LC95 and LC99 values in order to compare the larvicidal potency of the ten plants. Marked larvicidal effects were seen with Kaempferia galanga, Illicium vernum and Spilanthes acmella having LC50 values of 50.54, 54.11 and 61.43 ppm, respectively.

  17. Screening for larvicidal activity of ten carminative plants.

    PubMed

    Pitasawat, B; Choochote, W; Kanjanapothi, D; Panthong, A; Jitpakdi, A; Chaithong, U

    1998-09-01

    Ten species of plants, reported to possess carminative property, were screened for larvicidal potential against Culex quinquefasciatus by exposing early 4th instar larvae to a series of concentrations of the ethanolic extracts of the plants. Mortality counts were made after 24 hours exposure. Probit analysis using computerized Harvard Programming (Hg1, 2) was employed to determine the LC50, LC95 and LC99 values in order to compare the larvicidal potency of the ten plants. Marked larvicidal effects were seen with Kaempferia galanga, Illicium vernum and Spilanthes acmella having LC50 values of 50.54, 54.11 and 61.43 ppm, respectively. PMID:10437975

  18. Tailoring oxides of copper-Cu2O and CuO nanoparticles and evaluation of organic dyes degradation

    NASA Astrophysics Data System (ADS)

    Raghav, Ragini; Aggarwal, Priyanka; Srivastava, Sudha

    2016-04-01

    We report a simple one-pot colloidal synthesis strategy tailoring cuprous or cupric nano-oxides in pure state. NaOH provided alkaline conditions (pH 12.5 -13) for nano-oxides formation, while its concentration regulated the oxidation state of the nano-oxides. The morphological, structural and optical properties of synthesized Cu2O and CuO nanoparticles were studied by transmission electron microscopy (TEM), X-Ray diffraction (XRD) and UV-vis spectroscopy. Dye degradation capability of CuO and Cu2O nanoparticles was evaluated using four organic dyes - Malachite green, Methylene blue, Methyl orange and Methyl red. The results demonstrate effective degradation of all four dyes employing with almost comparable activity both Cu2O and CuO nanoparticles.

  19. Photoinduced absorption measurement on a microchip equipped with organic dye-doped polymer waveguide

    NASA Astrophysics Data System (ADS)

    Kawaguchi, T.; Nagai, K.; Yamashita, K.

    2013-05-01

    We have fabricated a waveguide-type optical sensing microchip and succeeded in on-chip photoinduced absorption (PIA) spectroscopy. The PIA microchip was fabricated with a conventional photolithographic technique and consisted of plastic optical waveguides and microfluidic channels. Furthermore, a serially-cascaded polymer waveguide doped with organic dyes was integrated on this microchip, which was fabricated using a self-written waveguide process. This dye-doped waveguide was pumped by a UV light emitting diode (UV-LED) and used as a probe light source with a broad emission spectrum. At the same time, a solution of test material in the microfluidic channel was synchronously pumped by a UV-LED or UV laser diode. Since the transmission spectrum of the photo-excited test material could be measured, the PIA spectra were obtained easily. In this study, we have demonstrated the on-chip PIA measurements for two classes of test materials, rare-earth complex and chlorophyll molecules. In the measurement for the aqueous solution of Neodymium (III) acetate hydrate, PIA signals attributed to the 4f-4f transition was observed. Furthermore, by varying the modulation frequency of the pulsed optical pumping, lifetime analysis of the excited 4f states was achieved. In the measurements for the ethanol solutions of chlorophyll a and chlorophyll b, PIA signals were observed at the wavelength near the Q-band absorption peaks. These spectra were very similar to the well-known feature for the photosystem II protein complex observed in a conventional PIA system. From these results, it is expected that the onchip PIA measurement technique is applicable to the transient analyses for the material systems with photoexcited charge transfer.

  20. Theoretical analysis of the absorption spectra of organic dyes differing by the conjugation sequence: illusion of negative solvatochromism

    NASA Astrophysics Data System (ADS)

    Manzhos, Sergei; Segawa, Hiroshi; Yamashita, Koichi

    2012-06-01

    Absorption peak maxima of two organic dyes differing by the position of the methine unit differ by 61 nm in dioxane and 128 nm in acetonnitrile. The difference is not reproduced by TDDFT using ab initio or hybrid functionals. TDDFT errors are different between the molecules due to a different albeit small extent of charge transfer, leading to a qualitative failure of TDDFT to predict relative energetics of the dyes. The TDDFT errors in non-polar solvents (such as dioxane) could be corrected based on the approach of Peach et al. (J. Chem. Phy. 128, 044118 (2008)). Here, we focus on the effect on the absorption spectrum of a polar solvent, specifically of the different between the two molecules sign of the solvatochromic shift vs. dioxane. Using the corrrection due to Peach et al, the absolute TDDFT errors can be brought within accetable ranges of 0.2-0.3 eV with the PCM solvent model, and the blue shift vs.dioxane is reporoduced, although both dyes are predicted to exhibit positive solvatochromism. The inclusion of explicit solvent molecules forming hydrogen bonds with the dye did not appreciably change neither TDDFT energies nor the correction term. These results show the importance of a more careful assessment of computational errors in the strategy of computationaly dye design by changing the conjugation order, where they are expected to be more important than in the case of an extension of the size of conjugation, and more so when polar solvents are used.

  1. Photoconductivity of organic polymer films doped with porous silicon nanoparticles and ionic polymethine dyes

    SciTech Connect

    Davidenko, N. A. Skrichevsky, V. A.; Ishchenko, A. A.; Karlash, A. Yu.; Mokrinskaya, E. V.

    2009-05-15

    Features of electrical conductivity and photoconductivity of polyvinylbutyral films containing porous silicon nanoparticles and similar films doped with cationic and anionic polymethine dyes are studied. Sensitization of the photoelectric effect by dyes with different ionicities in films is explained by the possible photogeneration of holes and electrons from dye molecules and the intrinsic bipolar conductivity of porous silicon nanoparticles. It is assumed that the electronic conductivity in porous silicon nanoparticles is higher in comparison with p-type conductivity.

  2. Irradiation of Escherichia coli in the Visible Spectrum with a Tunable Organic-Dye Laser Energy Source

    PubMed Central

    Takahashi, Patrick K.; Toups, Harold J.; Greenberg, David B.; Dimopoullos, George T.; Rusoff, Louis L.

    1975-01-01

    Pulsed laser energy was shown to be effective in inhibiting the growth of Escherichia coli. The irradiation source was derived from a tunable organic-dye laser utilizing rhodamine 6G (590 ± 5 nm) solutions as lasing media. The organisms, suspended in nutrient broth, were irradiated both with and without an exogenous photosensitizer. One photosensitizer (toluidine blue) did not appreciably alter the inhibitory effect observed. In the presence of acridine orange, however, some additional growth occurred. PMID:1089163

  3. Theoretical study of an asymmetric A-π-D-π-D-π-A' tribranched organic sensitizer for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Lee, Geon Hyeong; Kim, Young Sik

    2016-08-01

    An asymmetric A-π-D-π-D-π-A' tribranched organic dye (dye1) with cyanoacrylic acid and indolinum carboxyl acid as electron acceptors and triphenylamine as an electron donor was designed and theoretically investigated for dye-sensitized solar cells (DSSCs). Dye1 was compared to reference well-known dyes with single electron acceptors (D5 and JYL-SQ6). Density functional theory and time-dependent density functional theory calculations were used to estimate the photovoltaic properties of the dyes. Due to the different lowest unoccupied molecular orbital levels of each acceptor and the energy antenna of the dual electron donor (D-π-D), the absorption spectra of the branches displayed different shapes. If the overall properties are considered, the asymmetric A-π-D-π-D-π-A' tribranched organic dye exhibited a high conversion efficiency performance for DSSCs. The findings of this work suggest that optimizing the branch of electron donors and acceptors in dye sensitizers based on asymmetric A-π-D-π-D-π-A' tribranched organic dye produces good photovoltaic properties for DSSCs.

  4. Removal of organic dyes using Cr-containing activated carbon prepared from leather waste.

    PubMed

    Oliveira, Luiz C A; Coura, Camila Van Zanten; Guimarães, Iara R; Gonçalves, Maraisa

    2011-09-15

    In this work, hydrogen peroxide decomposition and oxidation of organics in aqueous medium were studied in the presence of activated carbon prepared from wet blue leather waste. The wet blue leather waste, after controlled pyrolysis under CO(2) flow, was transformed into chromium-containing activated carbons. The carbon with Cr showed high microporous surface area (up to 889 m(2)g(-1)). Moreover, the obtained carbon was impregnated with nanoparticles of chromium oxide from the wet blue leather. The chromium oxide was nanodispersed on the activated carbon, and the particle size increased with the activation time. It is proposed that these chromium species on the carbon can activate H(2)O(2) to generate HO radicals, which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. In fact, in this work we observed that activated carbon obtained from leather waste presented high removal of methylene blue dye combining the adsorption and oxidation processes.

  5. Abatements of reduced sulphur compounds, colour, and organic matter from indigo dyeing effluents by electrocoagulation.

    PubMed

    Tünay, Olcay; Simşeker, Merve; Kabdaşli, Isik; Olmez-Hanci, Tugba

    2014-08-01

    In the present study, the treatability of indigo dyeing effluents by the electrocoagulation (EC) process using stainless steel electrodes was experimentally investigated. The samples used were concentrated with main pollutant parameters of chemical oxygen demand (COD) (1000-1100 mg/L), reduced sulphur species (over 2000 mg SO2-(3)/L), and colour (0.12-0.13 1/cm). The study focused on the effect of main operation parameters on the EC process performance in terms of abatement of reduced sulphur compounds as well as decolourization and organic matter reduction. Results indicated that the performance of EC proved to be high providing total oxidation of the reduced sulphur compounds, almost complete decolourization, and COD removal up to 90%. Increasing applied current density from 22.5 to 45 mA/cm2 appreciably improved abatement of the reduced sulphur compounds for Sample I, but a further increase in the applied current density to 67.5 mA/cm2 did not accelerate the conversion rate to sulphate. The process performance was adversely affected by increasing initial concentration of the reduced sulphur compounds. Decolourization and organic matter removal efficiency enhanced with increasing applied current density. The main removal mechanism of the reduced sulphur compounds by EC was explained as conversion to sulphate via oxidation. Conversion rate to sulphate fitted pseudo-first-order kinetics very well.

  6. Energy-Cascaded Upconversion in an Organic Dye-Sensitized Core/Shell Fluoride Nanocrystal.

    PubMed

    Chen, Guanying; Damasco, Jossana; Qiu, Hailong; Shao, Wei; Ohulchanskyy, Tymish Y; Valiev, Rashid R; Wu, Xiang; Han, Gang; Wang, Yan; Yang, Chunhui; Ågren, Hans; Prasad, Paras N

    2015-11-11

    Lanthanide-doped upconversion nanoparticles hold promises for bioimaging, solar cells, and volumetric displays. However, their emission brightness and excitation wavelength range are limited by the weak and narrowband absorption of lanthanide ions. Here, we introduce a concept of multistep cascade energy transfer, from broadly infrared-harvesting organic dyes to sensitizer ions in the shell of an epitaxially designed core/shell inorganic nanostructure, with a sequential nonradiative energy transfer to upconverting ion pairs in the core. We show that this concept, when implemented in a core-shell architecture with suppressed surface-related luminescence quenching, yields multiphoton (three-, four-, and five-photon) upconversion quantum efficiency as high as 19% (upconversion energy conversion efficiency of 9.3%, upconversion quantum yield of 4.8%), which is about ~100 times higher than typically reported efficiency of upconversion at 800 nm in lanthanide-based nanostructures, along with a broad spectral range (over 150 nm) of infrared excitation and a large absorption cross-section of 1.47 × 10(-14) cm(2) per single nanoparticle. These features enable unprecedented three-photon upconversion (visible by naked eye as blue light) of an incoherent infrared light excitation with a power density comparable to that of solar irradiation at the Earth surface, having implications for broad applications of these organic-inorganic core/shell nanostructures with energy-cascaded upconversion.

  7. A metal-organic tetrahedron as a redox vehicle to encapsulate organic dyes for photocatalytic proton reduction.

    PubMed

    Jing, Xu; He, Cheng; Yang, Yang; Duan, Chunying

    2015-03-25

    The design of artificial systems that mimic highly evolved and finely tuned natural photosynthetic systems is a subject of intensive research. We report herein a new approach to constructing supramolecular systems for the photocatalytic generation of hydrogen from water by encapsulating an organic dye molecule into the pocket of a redox-active metal-organic polyhedron. The assembled neutral Co4L4 tetrahedron consists of four ligands and four cobalt ions that connect together in alternating fashion. The cobalt ions are coordinated by three thiosemicarbazone NS chelators and exhibit a redox potential suitable for electrochemical proton reduction. The close proximity between the redox site and the photosensitizer encapsulated in the pocket enables photoinduced electron transfer from the excited state of the photosensitizer to the cobalt-based catalytic sites via a powerful pseudo-intramolecular pathway. The modified supramolecular system exhibits TON values comparable to the highest values reported for related cobalt/fluorescein systems. Control experiments based on a smaller tetrahedral analogue of the vehicle with a filled pocket and a mononuclear compound resembling the cobalt corner of the tetrahedron suggest an enzymatic dynamics behavior. The new, well-elucidated reaction pathways and the increased molarity of the reaction within the confined space render these supramolecular systems superior to other relevant systems.

  8. Organic Dye Effects on DNAPL Entry Pressure in Water Saturated Porous Media

    SciTech Connect

    Iversen, G.M.

    2001-10-02

    One of three diazo dyes with the same fundamental structure have been used in most studies of DNAPL behavior in porous media to stain the NAPL: Sudan III, Sudan IV, or Oil-Red-O. The dyes are generally implicitly assumed to not influence DNAPL behavior. That assumption was tested using simple entry pressure experiments.

  9. Bio-Inspired electro-photonic structure for organic and dye sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Lopez, Rene

    2011-03-01

    A major challenge in solar cell technology dwells in achieving an efficient absorption of photons with an effective carrier extraction. In all cases, light absorption considerations call for thicker modules while carrier transport would benefit from thinner ones. This dichotomy is a fundamental problem limiting the efficiencies of most photovoltaics. One pathway to overcome this problem is to decouple light absorption from carrier collection. We present solutions to this problem applying bio-inspired nanostructures to two different types of systems: organic photovoltaic (OPV) and dye sensitized solar cells (DSSC). For OPV devices based on poly-3-hexylthiophene:[6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PCBM), we describe a 2-D photonic crystal geometry that enhances the absorption of polymer-fullerene photonic cells ~ 20 % relative to conventional planar cells. Remarkably, the photonic crystal cell offers the possibility to increase photocurrents by improvements in optical absorption and carrier extraction simultaneously, and particularly through the excitation of photonic resonant modes near the band edge of organic PV materials. We also present an optical method to extract charge transport lengths from device photoactive layers. For DSSCs we introduce a new structural motif for the photoanode in which the traditional random nanoparticle oxide network is replaced by vertically aligned bundles of oxide nanocrystals. We have used a pulsed laser deposition system to ablate titanium oxide targets to obtain the porous and vertically aligned structures for enhanced photoelectrochemical performance. Absorption studies show that in optimized structures for titanium oxide, there is a 1.4 times enhancement of surface area compared to the best sol-gel films, Incident-Photon-Conversion-Efficiency values are better than 3 times thicker sol-gel films, and ~ 92 % Absorbed-Photon-Conversion-Efficiency values have been observed when sensitizing with the N3 dye (Ru(dcbpyH)2

  10. Synthesis of magnetic metal-organic framework (MOF) for efficient removal of organic dyes from water.

    PubMed

    Zhao, Xiaoli; Liu, Shuangliu; Tang, Zhi; Niu, Hongyun; Cai, Yaqi; Meng, Wei; Wu, Fengchang; Giesy, John P

    2015-01-01

    A novel, simple and efficient strategy for fabricating a magnetic metal-organic framework (MOF) as sorbent to remove organic compounds from simulated water samples is presented and tested for removal of methylene blue (MB) as an example. The novel adsorbents combine advantages of MOFs and magnetic nanoparticles and possess large capacity, low cost, rapid removal and easy separation of the solid phase, which makes it an excellent sorbent for treatment of wastewaters. The resulting magnetic MOFs composites (also known as MFCs) have large surface areas (79.52 m(2) g(-1)), excellent magnetic response (14.89 emu g(-1)), and large mesopore volume (0.09 cm(3) g(-1)), as well as good chemical inertness and mechanical stability. Adsorption was not drastically affected by pH, suggesting π-π stacking interaction and/or hydrophobic interactions between MB and MFCs. Kinetic parameters followed pseudo-second-order kinetics and adsorption was described by the Freundlich isotherm. Adsorption capacity was 84 mg MB g(-1) at an initial MB concentration of 30 mg L(-1), which increased to 245 mg g(-1) when the initial MB concentration was 300 mg L(-1). This capacity was much greater than most other adsorbents reported in the literature. In addition, MFC adsorbents possess excellent reusability, being effective after at least five consecutive cycles. PMID:26149818

  11. Synthesis of magnetic metal-organic framework (MOF) for efficient removal of organic dyes from water

    PubMed Central

    Zhao, Xiaoli; Liu, Shuangliu; Tang, Zhi; Niu, Hongyun; Cai, Yaqi; Meng, Wei; Wu, Fengchang; Giesy, John P.

    2015-01-01

    A novel, simple and efficient strategy for fabricating a magnetic metal-organic framework (MOF) as sorbent to remove organic compounds from simulated water samples is presented and tested for removal of methylene blue (MB) as an example. The novel adsorbents combine advantages of MOFs and magnetic nanoparticles and possess large capacity, low cost, rapid removal and easy separation of the solid phase, which makes it an excellent sorbent for treatment of wastewaters. The resulting magnetic MOFs composites (also known as MFCs) have large surface areas (79.52 m2 g−1), excellent magnetic response (14.89 emu g−1), and large mesopore volume (0.09 cm3 g−1), as well as good chemical inertness and mechanical stability. Adsorption was not drastically affected by pH, suggesting π–π stacking interaction and/or hydrophobic interactions between MB and MFCs. Kinetic parameters followed pseudo-second-order kinetics and adsorption was described by the Freundlich isotherm. Adsorption capacity was 84 mg MB g−1 at an initial MB concentration of 30 mg L−1, which increased to 245 mg g−1 when the initial MB concentration was 300 mg L−1. This capacity was much greater than most other adsorbents reported in the literature. In addition, MFC adsorbents possess excellent reusability, being effective after at least five consecutive cycles. PMID:26149818

  12. Synthesis of magnetic metal-organic framework (MOF) for efficient removal of organic dyes from water

    NASA Astrophysics Data System (ADS)

    Zhao, Xiaoli; Liu, Shuangliu; Tang, Zhi; Niu, Hongyun; Cai, Yaqi; Meng, Wei; Wu, Fengchang; Giesy, John P.

    2015-07-01

    A novel, simple and efficient strategy for fabricating a magnetic metal-organic framework (MOF) as sorbent to remove organic compounds from simulated water samples is presented and tested for removal of methylene blue (MB) as an example. The novel adsorbents combine advantages of MOFs and magnetic nanoparticles and possess large capacity, low cost, rapid removal and easy separation of the solid phase, which makes it an excellent sorbent for treatment of wastewaters. The resulting magnetic MOFs composites (also known as MFCs) have large surface areas (79.52 m2 g-1), excellent magnetic response (14.89 emu g-1), and large mesopore volume (0.09 cm3 g-1), as well as good chemical inertness and mechanical stability. Adsorption was not drastically affected by pH, suggesting π-π stacking interaction and/or hydrophobic interactions between MB and MFCs. Kinetic parameters followed pseudo-second-order kinetics and adsorption was described by the Freundlich isotherm. Adsorption capacity was 84 mg MB g-1 at an initial MB concentration of 30 mg L-1, which increased to 245 mg g-1 when the initial MB concentration was 300 mg L-1. This capacity was much greater than most other adsorbents reported in the literature. In addition, MFC adsorbents possess excellent reusability, being effective after at least five consecutive cycles.

  13. High-performance plastic dye-sensitized solar cells based on low-cost commercial P25 TiO2 and organic dye.

    PubMed

    Yin, Xiong; Xue, Zhaosheng; Wang, Long; Cheng, Yueming; Liu, Bin

    2012-03-01

    High-performance plastic dye-sensitized solar cells (DSCs) based on low-cost commercial Degussa P25 TiO(2) and organic indoline dye D149 have been fabricated using electrophoretic deposition (EPD) with compression post-treatment at room temperature. The pressed EPD electrode outperformed the sintered EPD electrode and as-prepared EPD electrode in short-circuit current density and power conversion efficiency. About 150% and 180% enhancement in power conversion efficiency have been achieved in DSC devices with sintering and compression post-treatment as compared to the as-prepared electrode, respectively. Several characterizations including intensity modulated photocurrent spectroscopy, incident photon-to-electron conversion efficiency and electrochemical impedance spectra have been employed to reveal the nature of improvement with post-treatment. Experimental results indicate that the sintering and compression post-treatment are beneficial to improve the electron transport and thus lead to the enhancement of photocurrent and power conversion efficiency. In addition, the compression post-treatment is more efficient than sintering post-treatment in improving interparticle connection in the as-prepared EPD electrode. Under optimized conditions, the conversion efficiency of plastic devices with D149-sensitized P25 TiO(2) photoanode has reached 5.76% under illumination of AM 1.5G (100 mW cm(-2)). This study demonstrates that the EPD combined with compression post-treatment provides a way to fabricate highly efficient plastic photovoltaic devices.

  14. Quantitative determination of carmine in foods by high-performance liquid chromatography.

    PubMed

    Lim, Ho-Soo; Choi, Jae-Chon; Song, Sung-Bong; Kim, Meehye

    2014-09-01

    A simple and rapid method has been developed and validated for the determination of carmine in foods. Samples were homogenised and extracted with 0.05 M NaOH, followed by centrifugation. The resulting solution was filtered and injected to HPLC. Carmine was separated by HPLC using an NovaPak C18 column coupled to a photodiode array detector. The contents of carmine were finally quantified using corresponding calibration curves over ranges of 1.0-100 μg ml(-1), with good correlation coefficients (r(2)=0.9999). The recoveries of carmine from foods spiked at levels of 10, 50, and 100 μg g(-1) which ranged from 90.4% to 96.2% with relative standard deviations between 2.8% and 6.8%. Limit of detection and limit of quantification of carmine were 0.4 and 1.0 μg ml(-1), respectively. This method was found to be useful to distinguish carmine from carminic acid, a major component of cochineal extract. The method has been successfully applied to various foods. PMID:24731378

  15. HPLC-DAD-MS analysis of dyes identified in textiles from Mount Athos.

    PubMed

    Mantzouris, Dimitrios; Karapanagiotis, Ioannis; Valianou, Lemonia; Panayiotou, Costas

    2011-03-01

    Organic colorants contained in 30 textiles (16th to early 20th century) from the monastery of Simonos Petra (Mount Athos) have been investigated using high-performance liquid chromatography equipped with diode-array detection and mass spectrometry (HPLC-DAD-MS). The components of natural dyes identified in samples treated by the standard HCl dyestuff extraction method were: alizarin, apigenin, butein, carminic acid, chrysoeriol, dcII, dcIV, dcVII, ellagic acid, emodin, fisetin, flavokermesic acid, fustin, genistein, haematein derivative (Hae'), indigotin, indirubin, isoliquiritigenin, isorhamnetin, kaempferide, kaempferol, kermesic acid, luteolin, naringenin, purpurin, quercetin, rhamnazin, rhamnetin, sulfuretin, and type B and type C compounds (last two are markers for Caesalpinia trees). Early, semi-synthetic dyes, for example indigo carmine, fuchsin components, and rhodamine B were identified in objects dated late 19th to early 20th century. A dyestuff extraction method which involves use of TFA, instead of HCl, was applied to selected historical samples, showing that the mild method enables efficient extraction of weld (Reseda luteola L.) and dyer's broom (Genista tinctoria L.) glycosides. The marker compound (Hae') for logwood (Haematoxylum campechianum L.) identification after treatment with HCl was investigated by liquid chromatography coupled to mass spectrometry (LC-MS) in negative electrospray ionization (LC-MS-ESI(-)) mode. LC-MS in negative atmospheric pressure chemical ionization (LC-MS-APCI(-)) mode was used, probably for the first time, to investigate cochineal (Dactylopius coccus Costa) samples. Positive electrospray ionization (LC-MS-ESI(+)) mode was used for identification of fuchsin components. Detailed HPLC-DAD studies were performed on young fustic (Cotinus coggygria Scop.) and Persian berries (Rhamnus trees). PMID:21271239

  16. Surface Binding and Organization of Sensitizing Dyes on Metal Oxide Single Crystal Surfaces

    SciTech Connect

    Parkinson, Bruce

    2010-06-04

    Even though investigations of dye-sensitized nanocrystalline semiconductors in solar cells has dominated research on dye-sensitized semiconductors over the past two decades. Single crystal electrodes represent far simpler model systems for studying the sensitization process with a continuing train of studies dating back more than forty years. Even today single crystal surfaces prove to be more controlled experimental models for the study of dye-sensitized semiconductors than the nanocrystalline substrates. We analyzed the scientific advances in the model sensitized single crystal systems that preceded the introduction of nanocrystalline semiconductor electrodes. It then follows the single crystal research to the present, illustrating both their striking simplicity of use and clarity of interpretation relative to nanocrystalline electrodes. Researchers have employed many electrochemical, photochemical and scanning probe techniques for studying monolayer quantities of sensitizing dyes at specific crystallographic faces of different semiconductors. These methods include photochronocoulometry, electronic spectroscopy and flash photolysis of dyes at potential-controlled semiconductor electrodes and the use of total internal reflection methods. In addition, we describe the preparation of surfaces of single crystal SnS2 and TiO2 electrodes to serve as reproducible model systems for charge separation at dye sensitized solar cells. This process involves cleaving the SnS2 electrodes and a photoelectrochemical surface treatment for TiO2 that produces clean surfaces for sensitization (as verified by AFM) resulting in near unity yields for electron transfer from the molecular excited dyes into the conduction band.

  17. Hydrogen evolution by photocatalytic reactions of some organic dyes and semiconductors

    NASA Astrophysics Data System (ADS)

    Sakata, T.; Kawai, T.; Koiso, T.; Okuyama, M.

    Various organic dyes and powdered semiconductors are illuminated by visible light to bring about methylviologen - MV(2+) - reduction and hydrogen evolution from water, in an effort to study an 'artificial photosynthesis' process. MV(2+) is used as an electron acceptor, EDTA as an electron donor, and photochemical reactions are carried out both in nonaqueous solutions, such as dimethylsulfoxide, methanol, and in their mixtures with water. A 500W Xe lamp and a monochromator are used for monochromatic illumination at the peak wavelength of the visible absorption band of each molecule. The reduced MV(+) is monitored by a spectrophotometer, and a thermopile is used to determine the quantum efficiency of the reaction. Zn-chlorophyl-a and Zn-tetraphenylporphine show quite a high quantum efficiency. The preparation of the TiO2-RuO2 photocatalyst is described. The band gap illumination of TiO2 mixed with RuO2 leads to a continuous, catalytic production of hydrogen and oxygen from gaseous water at room temperature. The rate of hydrogen evolution per 100 mg of TiO2-RuO2, for 20 hours, is 11 micromoles at the stationary state.

  18. Investigation of 1H NMR chemical shifts of organic dye with hydrogen bonds and ring currents.

    PubMed

    Park, Sung Soo; Won, Yong Sun; Lee, Woojin; Kim, Jae Hong

    2011-04-01

    The (1)H NMR chemical shifts were theoretically computed for the organic dyes 2-(2,6-dimethyl-4H-pyran-4-ylidene)-malononitrile (1), cyano-(2,6-dimethyl-4H-pyran-4-ylidene)-acetic acid methyl ester (2), 2-(2,6-bis(4-(dimethylamino)styryl)-4H-pyran-4-ylidene)-malononitrile (3), and methyl 2-(2,6-bis(4-(dimethylamino)styryl)-4H-pyran-4-ylidene)-2-cyanoacetate (4) at the GIAO/B3LYP/6-311++G(d,p)//B3LYP/6-311++G(d,p) level of theory. Moreover, the intramolecular rotational barriers of the molecules were calculated to evaluate the internal flexibility with respect to the torsional degrees of freedom, and the nuclear-independent chemical shifts (NICS) were employed to analyze the ring currents. The difference was explained in terms of intramolecular hydrogen bonds and ring currents of the molecules. The (1)H NMR spectra were reproduced by experiments for the comparison with computationally constructed data. Our results suggest a good guideline in interpreting (1)H NMR chemical shifts using computational methods and furthermore a reliable perspective for designing molecular structures.

  19. Template-free hydrothermal derived cobalt oxide nanopowders: Synthesis, characterization, and removal of organic dyes

    SciTech Connect

    Nassar, Mostafa Y.; Ahmed, Ibrahim S.

    2012-09-15

    Graphical abstract: XRD patterns of the products obtained by hydrothermal treatment at 160 °C for 24 h, and at different [Co{sup 2+}]/[CO{sub 3}{sup 2−}] ratios: (a) 1:6, (b) 1:3, (c) 1:1.5, (d) 1:1, (e) 1:0.5. Highlights: ► Spinel cobalt oxide nanoparticles with different morphologies were prepared by hydrothermal approach. ► The optical characteristics of the as-prepared cobalt oxide revealed the presence of two band gaps. ► Adsorption of methylene blue dye on Co{sub 3}O{sub 4} was investigated and the percent uptake was found to be >99% in 24 h. -- Abstract: Pure spinel cobalt oxide nanoparticles were prepared through hydrothermal approach using different counter ions. First, the pure and uniform cobalt carbonate (with particle size of 21.8–29.8 nm) were prepared in high yield (94%) in an autoclave in absence unfriendly organic surfactants or solvents by adjusting different experimental parameters such as: pH, reaction time, temperature, counter ions, and (Co{sup 2+}:CO{sub 3}{sup 2−}) molar ratios. Thence, the spinel Co{sub 3}O{sub 4} (with mean particle size of 30.5–47.35 nm) was produced by thermal decomposition of cobalt carbonate in air at 500 °C for 3 h. The products were characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FTIR), transmission electron microscope (TEM), scanning electron microscope (SEM), and thermal analysis (TA). Also, the optical characteristics of the as-prepared Co{sub 3}O{sub 4} nanoparticles revealed the presence of two band gaps (1.45–1.47, and 1.83–1.93 eV). Additionally, adsorption of methylene blue dye on Co{sub 3}O{sub 4} nanoparticles was investigated and the uptake% was found to be >99% in 24 h.

  20. Preparation of graphene-ZrO2 nanocomposites by heat treatment and photocatalytic degradation of organic dyes.

    PubMed

    Cho, Bum Hwi; Ko, Weon Bae

    2013-11-01

    ZrO2 nanoparticles were synthesized by combining a solution containing zinconyl chloride in distilled water with a NH4OH solution under microwave irradiation. Graphene and ZrO2 nanocomposites were synthesized in an electric furnace at 700 degrees C for 2 hours. The heated graphene-ZrO2 nanocomposites were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. In addition, UV-vis spectrophotometry was used to evaluate the heated graphene-ZrO2 nanocomposites as a catalyst in the photocatalytic degradation of organic dyes. The photocatalytic effect of the heated graphene-ZrO2 nanocomposites was compared with that of unheated graphene nanoparticles, heated graphene nanoparticles, and unheated graphene-ZrO2 nanocomposites in organic dyes (methylene blue, methyl orange, and rhodamine B) under ultraviolet light at 254 nm.

  1. Preparation of graphene-ZrO2 nanocomposites by heat treatment and photocatalytic degradation of organic dyes.

    PubMed

    Cho, Bum Hwi; Ko, Weon Bae

    2013-11-01

    ZrO2 nanoparticles were synthesized by combining a solution containing zinconyl chloride in distilled water with a NH4OH solution under microwave irradiation. Graphene and ZrO2 nanocomposites were synthesized in an electric furnace at 700 degrees C for 2 hours. The heated graphene-ZrO2 nanocomposites were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. In addition, UV-vis spectrophotometry was used to evaluate the heated graphene-ZrO2 nanocomposites as a catalyst in the photocatalytic degradation of organic dyes. The photocatalytic effect of the heated graphene-ZrO2 nanocomposites was compared with that of unheated graphene nanoparticles, heated graphene nanoparticles, and unheated graphene-ZrO2 nanocomposites in organic dyes (methylene blue, methyl orange, and rhodamine B) under ultraviolet light at 254 nm. PMID:24245304

  2. Metal-organic frameworks derived carbon as a high-efficiency counter electrode for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Sun, Xun; Li, Yafeng; Dou, Jie; Shen, Deli; Wei, Mingdeng

    2016-08-01

    Metal-organic frameworks, ZIF-8, derived carbon materials are firstly applied as a counter electrode of dye-sensitized solar cells due to their easy fabrication, large specific surface area and high catalytic activities towards the reduction of I3- ions. An efficiency of 7.32% is achieved under the illumination of 1 sun (AM 1.5, 100 mW/cm2), which is comparable to that of the solar cell based on Pt electrode.

  3. Immobilization of papaya laccase in chitosan led to improved multipronged stability and dye discoloration.

    PubMed

    Jaiswal, Nivedita; Pandey, Veda P; Dwivedi, Upendra N

    2016-05-01

    A purified papaya laccase was immobilized in chitosan beads using entrapment approach and its physico-chemical properties were investigated and compared with that of free enzyme. Increase in properties of the laccase such as optimum temperature (by 10 °C), thermostability (by 3-folds) and optimum pH (from 8.0 to 10.0) was observed after immobilization. Immobilization led to increased tolerance of enzyme to a number of metal ions (including heavy metals) and organic solvents namely, ethanol, isopropanol, methanol, benzene and DMF. The catalytic efficiency (Kcat/Km) of the immobilized enzyme was found to increase more than ten folds, in comparison to that of the free enzyme, with hydroquinone as substrate. Immobilization of laccase also led to improvement in dye decolorization such that the synthetic dye indigo carmine (50 μg/ml) was completely decolorized within 8h of incubation as compared to that of the free laccase which decolorized the same dye to only 56% under similar conditions. Thus, immobilization of laccase into chitosan beads led to tremendous improvement in various useful attributes of this enzyme thereby making it more versatile for its industrial exploitation. PMID:26812115

  4. Peripheral Hole Acceptor Moieties on an Organic Dye Improve Dye‐Sensitized Solar Cell Performance

    PubMed Central

    Hao, Yan; Gabrielsson, Erik; Lohse, Peter William; Yang, Wenxing; Johansson, Erik M. J.; Hagfeldt, Anders

    2015-01-01

    Investigation of charge transfer dynamics in dye‐sensitized solar cells is of fundamental interest and the control of these dynamics is a key factor for developing more efficient solar cell devices. One possibility for attenuating losses through recombination between injected electrons and oxidized dye molecules is to move the positive charge further away from the metal oxide surface. For this purpose, a metal‐free dye named E6 is developed, in which the chromophore core is tethered to two external triphenylamine (TPA) units. After photoinduced electron injection into TiO2, the remaining hole is rapidly transferred to a peripheral TPA unit. Electron–hole recombination is slowed down by 30% compared to a reference dye without peripheral TPA units. Furthermore, it is found that the added TPA moieties improve the electron blocking effect of the dye, retarding recombination of electrons from TiO2 to the cobalt‐based electrolyte. PMID:27722076

  5. Induction, Purification and Characterization of a Novel Manganese Peroxidase from Irpex lacteus CD2 and Its Application in the Decolorization of Different Types of Dye

    PubMed Central

    Qin, Xing; Zhang, Jie; Zhang, Xiaoyu; Yang, Yang

    2014-01-01

    Manganese peroxidase (MnP) is the one of the important ligninolytic enzymes produced by lignin-degrading fungi which has the great application value in the field of environmental biotechnology. Searching for new MnP with stronger tolerance to metal ions and organic solvents is important for the maximization of potential of MnP in the biodegradation of recalcitrant xenobiotics. In this study, it was found that oxalic acid, veratryl alcohol and 2,6-Dimehoxyphenol could stimulate the synthesis of MnP in the white-rot fungus Irpex lacteus CD2. A novel manganese peroxidase named as CD2-MnP was purified and characterized from this fungus. CD2-MnP had a strong capability for tolerating different metal ions such as Ca2+, Cd2+, Co2+, Mg2+, Ni2+ and Zn2+ as well as organic solvents such as methanol, ethanol, DMSO, ethylene glycol, isopropyl alcohol, butanediol and glycerin. The different types of dyes including the azo dye (Remazol Brilliant Violet 5R, Direct Red 5B), anthraquinone dye (Remazol Brilliant Blue R), indigo dye (Indigo Carmine) and triphenylmethane dye (Methyl Green) as well as simulated textile wastewater could be efficiently decolorized by CD2-MnP. CD2-MnP also had a strong ability of decolorizing different dyes with the coexistence of metal ions and organic solvents. In summary, CD2-MnP from Irpex lacteus CD2 could effectively degrade a broad range of synthetic dyes and exhibit a great potential for environmental biotechnology. PMID:25412169

  6. Induction, purification and characterization of a novel manganese peroxidase from Irpex lacteus CD2 and its application in the decolorization of different types of dye.

    PubMed

    Qin, Xing; Zhang, Jie; Zhang, Xiaoyu; Yang, Yang

    2014-01-01

    Manganese peroxidase (MnP) is the one of the important ligninolytic enzymes produced by lignin-degrading fungi which has the great application value in the field of environmental biotechnology. Searching for new MnP with stronger tolerance to metal ions and organic solvents is important for the maximization of potential of MnP in the biodegradation of recalcitrant xenobiotics. In this study, it was found that oxalic acid, veratryl alcohol and 2,6-Dimehoxyphenol could stimulate the synthesis of MnP in the white-rot fungus Irpex lacteus CD2. A novel manganese peroxidase named as CD2-MnP was purified and characterized from this fungus. CD2-MnP had a strong capability for tolerating different metal ions such as Ca2+, Cd2+, Co2+, Mg2+, Ni2+ and Zn2+ as well as organic solvents such as methanol, ethanol, DMSO, ethylene glycol, isopropyl alcohol, butanediol and glycerin. The different types of dyes including the azo dye (Remazol Brilliant Violet 5R, Direct Red 5B), anthraquinone dye (Remazol Brilliant Blue R), indigo dye (Indigo Carmine) and triphenylmethane dye (Methyl Green) as well as simulated textile wastewater could be efficiently decolorized by CD2-MnP. CD2-MnP also had a strong ability of decolorizing different dyes with the coexistence of metal ions and organic solvents. In summary, CD2-MnP from Irpex lacteus CD2 could effectively degrade a broad range of synthetic dyes and exhibit a great potential for environmental biotechnology.

  7. 2,3-Dipentyldithieno[3,2-f:2',3'-h]quinoxaline-Based Organic Dyes for Efficient Dye-Sensitized Solar Cells: Effect of π-Bridges and Electron Donors on Solar Cell Performance.

    PubMed

    Huang, Zu-Sheng; Zang, Xu-Feng; Hua, Tao; Wang, Lingyun; Meier, Herbert; Cao, Derong

    2015-09-16

    Five novel metal-free organic dyes DQ1-5 containing a dipentyldithieno[3,2-f:2',3'-h]quinoxaline (DPQ) unit were synthesized and applied in dye-sensitized solar cells (DSSCs), where DPQ was employed as a π-spacer for the first time. Their photophysical, electrochemical, and theoretical calculations and photovoltaic properties were systematically investigated. All the five dyes show broad photoresponse. Especially the absorption edges of DQ3-5 extend to 800 nm on the TiO2 films. The inserted electron-rich unit 3,4-ethylenedioxythiophene or electron-withdrawing group benzothiadiazole (BTD) in DPQ-based dyes can greatly influence the optoelectronic properties of the dyes. In addition, the different electron donors also significantly affect the performance of the DSSCs. Under standard global AM 1.5 solar light conditions, the DQ5 sensitized solar cell obtained a power conversion efficiency of 7.12%. The result indicates that the rigid DPQ-based organic dye is a promising candidate for efficient DSSCs.

  8. Removal of malachite green dye from wastewater by different organic acid-modified natural adsorbent: kinetics, equilibriums, mechanisms, practical application, and disposal of dye-loaded adsorbent.

    PubMed

    Wang, Hou; Yuan, Xingzhong; Zeng, Guangming; Leng, Lijian; Peng, Xin; Liao, Kailingli; Peng, Lijuan; Xiao, Zhihua

    2014-10-01

    Natural adsorbent (Cinnamomum camphora sawdust) modified by organic acid (oxalic acid, citric acid, and tartaric acid) was investigated as a potential adsorbent for the removal of hazardous malachite green (MG) dye in aqueous media in a batch process. The extent of MG adsorption onto modified sawdust increased with increasing organic acid concentrations, pH, contact time, and temperature but decreased with increasing adsorbent dosage and ionic strength. Kinetic study indicated that the pseudo-second-order kinetic model could best describe the adsorption kinetics of MG. Equilibrium data were found to fit well with the Langmuir model, and the maximum adsorption capacity of the three kinds of organic acid-modified sawdust was 280.3, 222.8, and 157.5 mg/g, respectively. Thermodynamic parameters suggested that the sorption of MG was an endothermic process. The adsorption mechanism, the application of adsorbents in practical wastewater, the prediction of single-stage batch adsorption system, and the disposal of depleted adsorbents were also discussed.

  9. Microscopy of hierarchically organized TiO{sub 2} photoelectrode for dye solar cells

    SciTech Connect

    Eskandar, A.; Mohamed, N. M.

    2015-07-22

    Research on improving the performance of dye solar cells has various aspects of the device being investigated. This paper analyzes the deliberately hierarchized photoelectrode configuration for DSC applications to improve the performance of DSCs. Multiple layers of differently composed TiO{sub 2} particle types namely aggregates and nanoparticles were deposited to form a photoelectrode with thickness of about 12 µm. The photoelectrodes were assembled into working DSCs with an active area of 1 cm{sup 2}. Measurement for solar power conversion performance was measured under 1 sun at AM1.5 spectrum simulated sunlight. Electron microscopy for photoelectrode analysis was conducted using Field Emission Scattering Electron Microscopy with enhanced resolution. External Quantum Efficiency was measured using a purpose built instrument. Kinetics were investigated using the Electrochemical Impedance Spectroscopy (EIS) measurement with a potentiostat. The best performing DSC is of the hierarchically organized photoelectrode with a photoconversion efficiency of 4.58%, an increase of 14% in comparison to the reference samples with fully aggregates configuration. Short circuit current density, Jsc increases by about 2.223 mA cm{sup −2} relative to the blanks. The electron microscopy confirmed expected thickness at around 10 µm and layers forming the photoelectrode being hierarchically deposited with ∼20 nm TiO{sub 2} nanoparticles and 450 nm TiO{sub 2} aggregates mixture composition. EQE improved especially for visible region of 500-550 nm light wavelengths with 12 % increase in the response of in that region. Improvement to the diffusion coefficient as measured by the EIS contributed to the performance increase of the photoelectrode configuration under investigation.

  10. Synthesis and characterization of organic dyes with various electron-accepting substituents for p-type dye-sensitized solar cells.

    PubMed

    Weidelener, Martin; Powar, Satvasheel; Kast, Hannelore; Yu, Ze; Boix, Pablo P; Li, Chen; Müllen, Klaus; Geiger, Thomas; Kuster, Simon; Nüesch, Frank; Bach, Udo; Mishra, Amaresh; Bäuerle, Peter

    2014-11-01

    Four new donor-π-acceptor dyes differing in their acceptor group have been synthesized and employed as model systems to study the influence of the acceptor groups on the photophysical properties and in NiO-based p-type dye-sensitized solar cells. UV/Vis absorption spectra showed a broad range of absorption coverage with maxima between 331 and 653 nm. Redox potentials as well as HOMO and LUMO energies of the dyes were determined from cyclic voltammetry measurements and evaluated concerning their potential use as sensitizers in p-type dye-sensitized solar cells (p-DSCs). Quantum-chemical density functional theory calculations gave further insight into the frontier orbital distributions, which are relevant for the electronic processes in p-DSCs. In p-DSCs using an iodide/triiodide-based electrolyte, the polycyclic 9,10-dicyano-acenaphtho[1,2-b]quinoxaline (DCANQ) acceptor-containing dye gave the highest power conversion efficiency of 0.08%, which is comparable to that obtained with the perylenemonoimide (PMI)-containing dye. Interestingly, devices containing the DCANQ-based dye achieve a higher V(OC) of 163 mV compared to 158 mV for the PMI-containing dye. The result was further confirmed by impedance spectroscopic analysis showing higher recombination resistance and thus a lower recombination rate for devices containing the DCANQ dye than for PMI dye-based devices. However, the use of the strong electron-accepting tricyanofurane (TCF) group played a negative role in the device performance, yielding an efficiency of only 0.01% due to a low-lying LUMO energy level, thus resulting in an insufficient driving force for efficient dye regeneration. The results demonstrate that a careful molecular design with a proper choice of the acceptor unit is essential for development of sensitizers for p-DSCs.

  11. Thermoresponsive cellulose ether and its flocculation behavior for organic dye removal.

    PubMed

    Tian, Ye; Ju, Benzhi; Zhang, Shufen; Hou, Linan

    2016-01-20

    A thermoresponsive polymer, 2-hydroxy-3-butoxypropyl hydroxyethyl cellulose (HBPEC), was prepared by grafting butyl glycidyl ether (BGE) onto hydroxyethyl cellulose (HEC). The lower critical solution temperature (LCST) and critical flocculation temperature (CFT) of HBPEC were varied by changing the molar substitution (MS) and salt concentrations. Transmission electron microscopy (TEM) images and fluorescence spectroscopy showed that HBPEC can assemble into micelles. Additionally, using Nile Red as a model dye, the performance of HBPEC for the removing Nile Red from aqueous solutions via cloud point extraction procedures was investigated in detail. The encapsulation behavior of dye in the aqueous solution of HBPEC was studied by fluorescence spectroscopy and fluorescence microscope. The experimental results indicated that 99.4% of dye was removed from the aqueous solutions, and the HBPEC was recycled and reused easily, Furthermore, the recycle efficiency (RE) and maximum loading capacity portrayed little loss with the number of cycles.

  12. Clickable degradable aliphatic polyesters via copolymerization with alkyne epoxy esters: synthesis and postfunctionalization with organic dyes.

    PubMed

    Teske, Nele S; Voigt, Julia; Shastri, V Prasad

    2014-07-23

    Degradable aliphatic polyesters are the cornerstones of nanoparticle (NP)-based therapeutics. In this paradigm, covalent modification of the NP with cell-targeting motifs and dyes can aid in guiding the NP to its destination and gaining visual confirmation. Therefore, strategies to impart chemistries along the polymer backbone that are amenable to easy modification, such as 1,3-dipolar cycloaddition of an azide to an alkyne (the "click reaction"), could be significant. Here we present a simple and efficient way to introduce alkyne groups at high density in aliphatic polyesters without compromising their crystallinity via the copolymerization of cyclic lactones with propargyl 3-methylpentenoate oxide (PMPO). Copolymers of lactic acid and ε-caprolactone with PMPO were synthesized with up to 9 mol % alkyne content, and accessibility of the alkyne groups to the click reaction was demonstrated using several dyes commonly employed in fluorescence microscopy and imaging (Cy3, ATTO-740, and coumarin 343). In order to establish the suitability of these copolymers as nanocarriers, copolymers were formulated into NPs, and cytocompatibility, cellular uptake, and visualization studies undertaken in HeLa cells. Dye-modified NPs exhibited no quenching, remained stable in solution for at least 10 days, showed no cytotoxicity, and were readily taken up by HeLa cells. Furthermore, in addition to enabling the incorporation of multiple fluorophores within the same NP through blending of individual dye-modified copolymers, dye-modified polyesters offer advantages over physical entrapment of dye, including improved signal to noise ratio and localization of the fluorescence signal within cells, and possess the necessary prerequisites for drug delivery and imaging.

  13. An integrated experimental and theoretical approach to the spectroscopy of organic-dye-sensitized TiO₂ heterointerfaces: disentangling the effects of aggregation, solvation, and surface protonation.

    PubMed

    Marotta, Gabriele; Lobello, Maria Grazia; Anselmi, Chiara; Barozzino Consiglio, Gabriella; Calamante, Massimo; Mordini, Alessandro; Pastore, Mariachiara; De Angelis, Filippo

    2014-04-14

    We report a joint experimental and computational study into the spectroscopic properties of a prototypical D5 organic dye, both in solution and adsorbed on a TiO2 surface, with the aim of modeling and quantifying the UV/Vis spectral shifts that occur in the different explored environments. Going from the dye in solution to dye-sensitized TiO2, various factors may shift the position of the UV/Vis absorption maximum, both towards longer and shorter wavelengths. Here we have focused on the effect of dye aggregation on TiO2, surface protonation, and solvent effects. The D5 dye forms stable aggregates on the TiO2 surface that cause spectral blueshifts. We used different sensitization conditions to vary the dye loading and thus the extent of dye aggregation. For each sensitization condition, we explored protonated and native TiO2 films. Computational modeling of different dimeric aggregates with increasing intermolecular interactions and simulation of the associated optical responses also confirm the observed spectral blueshifts. Our results show that both the presence of surface protons and solvent stabilize the excited state of the adsorbed dye molecules, which causes a marked redshift in the absorption maximum and thus moves in the opposite direction to the shift due to the increase in the surface coverage.

  14. Response characterization of a fiber optic sensor array with dye-coated planar waveguide for detection of volatile organic compounds.

    PubMed

    Lee, Jae-Sung; Yoon, Na-Rae; Kang, Byoung-Ho; Lee, Sang-Won; Gopalan, Sai-Anand; Jeong, Hyun-Min; Lee, Seung-Ha; Kwon, Dae-Hyuk; Kang, Shin-Won

    2014-07-01

    We have developed a multi-array side-polished optical-fiber gas sensor for the detection of volatile organic compound (VOC) gases. The side-polished optical-fiber coupled with a polymer planar waveguide (PWG) provides high sensitivity to alterations in refractive index. The PWG was fabricated by coating a solvatochromic dye with poly(vinylpyrrolidone). To confirm the effectiveness of the sensor, five different sensing membranes were fabricated by coating the side-polished optical-fiber using the solvatochromic dyes Reinhardt's dye, Nile red, 4-aminophthalimide, 4-amino-N-methylphthalimide, and 4-(dimethylamino)cinnamaldehyde, which have different polarities that cause changes in the effective refractive index of the sensing membrane owing to evanescent field coupling. The fabricated gas detection system was tested with five types of VOC gases, namely acetic acid, benzene, dimethylamine, ethanol, and toluene at concentrations of 1, 2,…,10 ppb. Second-regression and principal component analyses showed that the response properties of the proposed VOC gas sensor were linearly shifted bathochromically, and each gas showed different response characteristics.

  15. Response Characterization of a Fiber Optic Sensor Array with Dye-Coated Planar Waveguide for Detection of Volatile Organic Compounds

    PubMed Central

    Lee, Jae-Sung; Yoon, Na-Rae; Kang, Byoung-Ho; Lee, Sang-Won; Gopalan, Sai-Anand; Jeong, Hyun-Min; Lee, Seung-Ha; Kwon, Dae-Hyuk; Kang, Shin-Won

    2014-01-01

    We have developed a multi-array side-polished optical-fiber gas sensor for the detection of volatile organic compound (VOC) gases. The side-polished optical-fiber coupled with a polymer planar waveguide (PWG) provides high sensitivity to alterations in refractive index. The PWG was fabricated by coating a solvatochromic dye with poly(vinylpyrrolidone). To confirm the effectiveness of the sensor, five different sensing membranes were fabricated by coating the side-polished optical-fiber using the solvatochromic dyes Reinhardt's dye, Nile red, 4-aminophthalimide, 4-amino-N-methylphthalimide, and 4-(dimethylamino)cinnamaldehyde, which have different polarities that cause changes in the effective refractive index of the sensing membrane owing to evanescent field coupling. The fabricated gas detection system was tested with five types of VOC gases, namely acetic acid, benzene, dimethylamine, ethanol, and toluene at concentrations of 1, 2,…,10 ppb. Second-regression and principal component analyses showed that the response properties of the proposed VOC gas sensor were linearly shifted bathochromically, and each gas showed different response characteristics. PMID:24988381

  16. Doping effects of fluorinated organic dyes on the open-circuit voltage of bulk-heterojunction photovoltaic devices

    NASA Astrophysics Data System (ADS)

    Watanabe, Tomoki; Yamashita, Kenichi

    2015-08-01

    We have investigated photovoltaic properties of bulk-heterojunction (BHJ) organic absorption layer doped with fluorinated Coumarin dyes. By dilute doping of a fluorinated Coumarin dye, Coumarin 307, into poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) BHJ absorption layer, the open-circuit voltage of photovoltaic device increased by ∼90 mV without the significant degradation in the short-circuit current density. On the other hand, the doping of non-fluorinated Coumarin dye such as Coumarin 2 did not induce such the enhancement effect in the open-circuit voltage. In ultraviolet photoelectron spectroscopies, the doping of Coumarin 307 was found to have no impact on P3HT, but the density of state of PCBM was significantly modified by the doping. The change in the density of state was confirmed also in ultraviolet absorption measurement. Possible explanations for the enhancement in the open-circuit voltage are discussed from the experimental results, and a shift of the vacuum level by the doping can be considered as a direct origin.

  17. Facile synthesis of PbWO4: Applications in photoluminescence and photocatalytic degradation of organic dyes under visible light

    NASA Astrophysics Data System (ADS)

    Saraf, Rohit; Shivakumara, C.; Behera, Sukanti; Nagabhushana, H.; Dhananjaya, N.

    2015-02-01

    Stolzite polymorph of PbWO4 catalyst was prepared by the facile room temperature precipitation method. Structural parameters were refined by the Rietveld analysis using powder X-ray data. PbWO4 was crystallized in the scheelite-type tetragonal structure with space group I41/a (No. 88). Field emission scanning electron microscopy revealed leaf like morphology. Photoluminescence spectra exhibit broad blue emission (425 nm) under the excitation of 356 nm. The photocatalytic degradation of Methylene blue, Rhodamine B and Methyl orange dyes were measured under visible illumination. The 100% dye degradation was observed for MB and RhB dyes within 60 and 105 min. The rate constant was found to be in the decreasing order of MB > RhB > MO which followed the 1st order kinetic mechanism. Therefore, PbWO4 can be a potential candidate for blue component in white LEDs and also acts as a catalyst for the treatment of toxic and non-biodegradable organic pollutants in water.

  18. Facile synthesis of PbWO4: applications in photoluminescence and photocatalytic degradation of organic dyes under visible light.

    PubMed

    Saraf, Rohit; Shivakumara, C; Behera, Sukanti; Nagabhushana, H; Dhananjaya, N

    2015-02-01

    Stolzite polymorph of PbWO4 catalyst was prepared by the facile room temperature precipitation method. Structural parameters were refined by the Rietveld analysis using powder X-ray data. PbWO4 was crystallized in the scheelite-type tetragonal structure with space group I41/a (No. 88). Field emission scanning electron microscopy revealed leaf like morphology. Photoluminescence spectra exhibit broad blue emission (425 nm) under the excitation of 356 nm. The photocatalytic degradation of Methylene blue, Rhodamine B and Methyl orange dyes were measured under visible illumination. The 100% dye degradation was observed for MB and RhB dyes within 60 and 105 min. The rate constant was found to be in the decreasing order of MB>RhB>MO which followed the 1st order kinetic mechanism. Therefore, PbWO4 can be a potential candidate for blue component in white LEDs and also acts as a catalyst for the treatment of toxic and non-biodegradable organic pollutants in water.

  19. A high surface area Zr(IV)-based metal–organic framework showing stepwise gas adsorption and selective dye uptake

    SciTech Connect

    Lv, Xiu-Liang; Tong, Minman; Huang, Hongliang; Wang, Bin; Gan, Lei; Yang, Qingyuan; Zhong, Chongli; Li, Jian-Rong

    2015-03-15

    Exploitation of new metal–organic framework (MOF) materials with high surface areas has been attracting great attention in related research communities due to their broad potential applications. In this work, a new Zr(IV)-based MOF, [Zr{sub 6}O{sub 4}(OH){sub 4}(eddb){sub 6}] (BUT-30, H{sub 2}eddb=4,4′-(ethyne-1,2-diyl)dibenzoic acid) has been solvothermally synthesized, characterized, and explored for gases and dyes adsorptions. Single-crystal X-ray diffraction analysis demonstrates a three-dimensional cubic framework structure of this MOF, in which each Zr{sub 6}O{sub 4}(OH){sub 4} building unit is linked by 12 linear eddb ligands. BUT-30 has been found stable up to 400 °C and has a Brunauer–Emmett–Teller (BET) surface area as high as 3940.6 m{sup 2} g{sup −1} (based on the N{sub 2} adsorption at 77 K) and total pore volume of 1.55 cm{sup 3} g{sup −1}. It is more interesting that this MOF exhibits stepwise adsorption behaviors for Ar, N{sub 2}, and CO{sub 2} at low temperatures, and selective uptakes towards different ionic dyes. - Graphical abstract: A new Zr(IV)-based MOF with high surface area has been synthesized and structurally characterized, which shows stepwise gas adsorption at low temperature and selective dye uptake from solution. - Highlights: • A new Zr-based MOF was synthesized and structurally characterized. • This MOF shows a higher surface area compared with its analogous UiO-67 and 68. • This MOF shows a rare stepwise adsorption towards light gases at low temperature. • This MOF performs selective uptakes towards cationic dyes over anionic ones. • Using triple-bond spacer is confirmed feasible in enhancing MOF surface areas.

  20. Rational Molecular Engineering of Indoline-Based D-A-π-A Organic Sensitizers for Long-Wavelength-Responsive Dye-Sensitized Solar Cells.

    PubMed

    Zhang, Weiwei; Wu, Yongzhen; Zhu, Haibo; Chai, Qipeng; Liu, Jingchuan; Li, Hui; Song, Xiongrong; Zhu, Wei-Hong

    2015-12-01

    Indoline-based D-A-π-A organic sensitizers are promising candidates for highly efficient and long-term stable dye-sensitized solar cells (DSSCs). In order to further broaden the spectral response of the known indoline dye WS-2, we rationally engineer the molecular structure through enhancing the electron donor and extending the π-bridge, resulting in two novel indoline-based D-A-π-A organic sensitizers WS-92 and WS-95. By replacing the 4-methylphenyl group on the indoline donor of WS-2 with a more electron-rich carbazole unit, the intramolecular charge transfer (ICT) absorption band of dye WS-92 is slightly red-shifted from 550 nm (WS-2) to 554 nm (WS-92). In comparison, the incorporation of a larger π-bridge of cyclopentadithiophene (CPDT) unit in dye WS-95 not only greatly bathochromatically tunes the absorption band to 574 nm but also largely enhances the molar extinction coefficients (ε), thus dramatically improving the light-harvesting capability. Under the standard global AM 1.5 solar light condition, the photovoltaic performances of both organic dyes have been evaluated in DSSCs on the basis of the iodide/triiodide electrolyte without any coadsorbent or cosensitizer. The DSSCs based on WS-95 display better device performance with power conversion efficiency (η) of 7.69%. The additional coadsorbent in the dye bath of WS-95 does not improve the photovoltaic performance, indicative of its negligible dye aggregation, which can be rationalized by the grafted dioctyl chains on the CPDT unit. The cosensitization of WS-95 with a short absorption wavelength dye S2 enhances the IPCE and improves the η to 9.18%. Our results indicate that extending the π-spacer is more rational than enhancing the electron donor in terms of broadening the spectral response of indoline-based D-A-π-A organic sensitizers.

  1. Superiority of D-A-D over D-A type of organic dyes for the application in dye-sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Biswas, Santu; Pramanik, Anup; Ahmed, Tasnim; Sahoo, Suman Kalyan; Sarkar, Pranab

    2016-04-01

    We study the optoelectronic properties of some recently synthesized D-A-D chromophores which are susceptible for superior intramolecular charge transfer (ICT) property. Our first principle calculations reveal that, the chromophores have enhanced charge transfer probability in the excited state in comparison to their corresponding ground states indicating faster electron injection at the interface of dye-semiconductor composites. We compute the photovoltaic properties of the dyes with and without substitution and way out a root for optimizing the device performance. Finally, dye-TiO2 QD composite systems are studied as a model for realistic photovoltaic device.

  2. Destination of organic pollutants during electrochemical oxidation of biologically-pretreated dye wastewater using boron-doped diamond anode.

    PubMed

    Zhu, Xiuping; Ni, Jinren; Wei, Junjun; Xing, Xuan; Li, Hongna

    2011-05-15

    Electrochemical oxidation of biologically-pretreated dye wastewater was performed in a boron-doped diamond (BDD) anode system. After electrolysis of 12h, the COD was decreased from 532 to 99 mg L(-1) (<100 mg L(-1), the National Discharge Standard of China). More importantly, the destination of organic pollutants during electrochemical oxidation process was carefully investigated by molecular weight distribution measurement, resin fractionation, ultraviolet-visible spectroscopy, HPLC and GC-MS analysis, and toxicity test. As results, most organic pollutants were completely removed by electrochemical oxidation and the rest was primarily degraded to simpler compounds (e.g., carboxylic acids and short-chain alkanes) with less toxicity, which demonstrated that electrochemical oxidation of biologically-pretreated dye wastewater with BDD anode was very effective and safe. Especially, the performance of BDD anode system in degradation of large molecular organics such as humic substances makes it very promising in practical applications as an advanced treatment of biologically-pretreated wastewaters. PMID:21377794

  3. Comparative study on the process behavior and reaction kinetics in sonocatalytic degradation of organic dyes by powder and nanotubes TiO2.

    PubMed

    Pang, Yean Ling; Abdullah, Ahmad Zuhairi

    2012-05-01

    Sonocatalytic degradation of various organic dyes (Congo Red, Reactive Blue 4, Methyl Orange, Rhodamine B and Methylene Blue) catalyzed by powder and nanotubes TiO(2) was studied. Both catalysts were characterized using transmission electron microscope (TEM), surface analyzer, Raman spectroscope and thermal gravimetric analyzer (TGA). Sonocatalytic activity of powder and nanotubes TiO(2) was elucidated based on the degradation of various organic dyes. The former catalyst was favorable for treatment of anionic dyes, while the latter was more beneficial for cationic dyes. Sonocatalytic activity of TiO(2) nanotubes could be up to four times as compared to TiO(2) powder under an ultrasonic power of 100 W and a frequency of 42 kHz. This was associated with the higher surface area and the electrostatic attraction between dye molecules and TiO(2) nanotubes. Fourier transform-infrared spectrometer (FT-IR) was used to identify changes that occurred on the functional group in Rhodamine B molecules and TiO(2) nanotubes after the reaction. Sonocatalytic degradation of Rhodamine B by TiO(2) nanotubes apparently followed the Langmuir-Hinshelwood adsorption kinetic model with surface reaction rate of 1.75 mg/L min. TiO(2) nanotubes were proven for their high potential to be applied in sonocatalytic degradation of organic dyes.

  4. Catalytic spectrophotometric determination of trace aluminium with indigo carmine

    NASA Astrophysics Data System (ADS)

    Zheng, Huai-Li; Xiong, Wen-Qiang; Gong, Ying-Kun; Peng, De-Jun; Li, Ling-Chun

    2007-04-01

    A new catalytic spectrophotometric method is described for the determination of trace amounts of Al(III). The methods based on catalytic action of Al(III) on the oxidation of indigo carmine (IC) by ammonium persulfate in hexamethylene tetramine-hydrochloric acid ((CH 2) 6N 4-HCl) buffer medium (pH 5.4) and in the presence of surfactant—TritonX-100. The effects of some factors on the reaction speed were investigated. Aluminium concentration is linear for 0-1.2 × 10 -7 g/ml in this method. The detection limit of the proposed method is 1.96 × 10 -8 g/ml. Most of the foreign ions except for Cu(II), Fe(III) do not interfere with the determination, and the interference of Cu(II) and Fe(III) in this method can be removed by extraction with sodium diethyldithiocarbamate-carbon tetrachloride (DDTC-CCl 4). This system is a quasi-zero-order reaction for Al(III), but it is a quasi-first-order reaction for IC. The apparent rate constant is 2.62 × 10 -5 s -1 and the apparent activation energy is 6.60 kJ/mol in the system. The proposed method was applied to the determination of trace aluminium(III) in real samples with satisfactory results.

  5. Self-organization and photo-induced formation of cyanine dye aggregates on the plasmonic Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Starovoytov, Anton A.; Nabiullina, Rezida D.; Toropov, Nikita A.

    2016-04-01

    The optical properties of hybrid film based on plasmon Ag nanoparticles of different size and cyanine dyes with different length of conjugation chain depending on the relative position of the plasmon resonance and the absorption of organic molecules were studied. The absorption spectra of the films revealed several molecular forms, such as all-trans- and cisisomers, dimers and J-aggregate, which also exist in pure organic films without Ag nanoparticles. It's shown that the absorption of aggregate bands increased after exposure by nanosecond laser on the hybrid films due to photo-induced additional self-organization of aggregates. In the presence of Ag nanoparticles, laser radiation leads to the change of molecular forms at a comparatively low threshold.

  6. ZnO double layer film with a novel organic sensitizer as an efficient photoelectrode for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Lee, Chuan-Pei; Chen, Ping-Wei; Li, Chun-Ting; Huang, Yi-June; Li, Sie-Rong; Chang, Ling-Yu; Chen, Pei-Yu; Lin, Lu-Yin; Vittal, R.; Sun, Shih-Sheng; Lin, Jiang-Jen; Ho, Kuo-Chuan

    2016-09-01

    A novel organic sensitizer, coded CR147, is applied to sensitize a ZnO-based dye-sensitized solar cell (DSSC). The common problem of ZnO dissolution and Zn2+/dye agglomeration, caused by the use of ruthenium-based dyes, is solved by the application of this CR147 dye. The highest power conversion efficiency (η) of 4.77% is achieved for the DSSC using a photoanode with a film of commercial ZnO nanoparticles (Csbnd ZnO) and the CR147 dye, while the η is only 3.41% for the DSSC with the commercial N719 dye. The cell performance with the CR147 dye is further improved by using a photoanode with the double layer ZnO film (D-ZnO), composed of an underlayer with coral-like ZnO nanocrystals and an overlayer with hexagonal club-like ZnO submicrocrystals. The DSSC with the D-ZnO film exhibits an η of 6.89%, which is ca. 45% higher than that of the DSSC with the Csbnd ZnO film (4.77%). This higher efficiency is attributed to the superior charge transfer and light-scattering abilities provided by coral-like ZnO nanocrystals and hexagonal clubs-like ZnO submicrocrystals, respectively, with reference to these parameters of Csbnd ZnO.

  7. The J-band of organic dyes: lineshape and coherence length

    NASA Astrophysics Data System (ADS)

    Eisfeld, Alexander; Briggs, John S.

    2002-07-01

    Self-organised J-aggregates of dye molecules, known for over 60 years, are emerging as remarkably versatile quantum systems with applications in photography, opto-electronics, solar cells, photobiology and as supra-molecular fibres. Recently there has been much effort to achieve quantum entanglement and coherence on the nanoscale in atom traps and quantum dot aggregates (for use in quantum computing). We point out that the excitonic state of the J-aggregate is a text-book case of mesoscopic quantum coherence and entanglement. The establishment of coherence can literally be seen since the dye changes colour dramatically on aggregation due to strong shifts in the absorption spectrum. Here we reproduce in a simple theory the shifts and shapes of optical absorption spectra upon aggregation to a polymer and calculate the coherence length of quantum entanglement of monomer wavefunctions.

  8. Color tuning in new metal-free organic sensitizers (Bodipys) for dye-sensitized solar cells.

    PubMed

    Kumaresan, Duraisamy; Thummel, Randolph P; Bura, Thomas; Ulrich, Gilles; Ziessel, Raymond

    2009-06-22

    Fun in the sun! A strategy has been devised for functionalizing and solubilizing boron dipyrromethene (Bodipy) dyes at the central boron atom and changing the color by increasing delocalization on the central core. This approach leads to the formation of stable B-C[triple bond]C and pyrrole--C=C linkages suitable for use in TiO(2)-sensitized devices (see figure).

  9. An organic dye-polymer (phenol red-poly (vinyl alcohol)) composite architecture towards tunable -optical and -saturable absorption characteristics

    NASA Astrophysics Data System (ADS)

    Sreedhar, Sreeja; Illyaskutty, Navas; Sreedhanya, S.; Philip, Reji; Muneera, C. I.

    2016-05-01

    Herein, we demonstrate that blending an organic dye (guest/filler), with a vinyl polymer (host template), is an inexpensive and simple approach for the fabrication of multifunctional photonic materials which could display an enhancement in the desirable properties of the constituent materials and, at the same time provide novel synergistic properties for the guest-host system. A new guest-host nanocomposite system comprising Phenol Red dye and poly (vinyl alcohol) as guest and host template, respectively, which exhibits tunable optical characteristics and saturable absorption behavior, is introduced. The dependence of local electronic environment provided by the polymer template and the interactions of the polymer molecules with the encapsulated guest molecules on the observed optical/nonlinear absorption behavior is discussed. An understanding of the tunability of the optical/ photophysical processes, with respect to the filler content, as discussed herein could help in the design of improved optical materials for several photonic device applications like organic light emitting diodes and saturable absorbers.

  10. Graphene Oxide/Silver Nanohybrid as Multi-functional Material for Highly Efficient Bacterial Disinfection and Detection of Organic Dye

    NASA Astrophysics Data System (ADS)

    Tam, Le Thi; Dinh, Ngo Xuan; Van Cuong, Nguyen; Van Quy, Nguyen; Huy, Tran Quang; Ngo, Duc-The; Mølhave, Kristian; Le, Anh-Tuan

    2016-10-01

    In this work, a multi-functional hybrid system consisting of graphene oxide and silver nanoparticles (GO-Ag NPs) was successfully synthesized by using a two-step chemical process. We firstly demonstrated noticeable bactericidal ability of the GO-Ag hybrid system. We provide more chemo-physical evidence explaining the antibacterial behavior of GO-Ag nanohybrid against Gram-negative Escherichia Coli and Gram-positive Staphylococcus aureus in light of ultrastructural damage analyses and Ag1+ ions release rate onto the cells/medium. A further understanding of the mode of antimicrobial action is very important for designing and developing advanced antimicrobial systems. Secondly, we have also demonstrated that the GO-Ag nanohybrid material could be used as a potential surface enhanced Raman scattering (SERS) substrate to detect and quantify organic dyes, e.g., methylene blue (MB), in aqueous media. Our findings revealed that the GO-Ag hybrid system showed better SERS performance of MB detection than that of pure Ag-NPs. MB could be detected at a concentration as low as 1 ppm. The GO-Ag-based SERS platform can be effectively used to detect trace concentrations of various types of organic dyes in aqueous media. With the aforementioned properties, the GO-Ag hybrid system is found to be very promising as a multi-functional material for advanced biomedicine and environmental monitoring applications.

  11. Graphene Oxide/Silver Nanohybrid as Multi-functional Material for Highly Efficient Bacterial Disinfection and Detection of Organic Dye

    NASA Astrophysics Data System (ADS)

    Tam, Le Thi; Dinh, Ngo Xuan; Van Cuong, Nguyen; Van Quy, Nguyen; Huy, Tran Quang; Ngo, Duc-The; Mølhave, Kristian; Le, Anh-Tuan

    2016-06-01

    In this work, a multi-functional hybrid system consisting of graphene oxide and silver nanoparticles (GO-Ag NPs) was successfully synthesized by using a two-step chemical process. We firstly demonstrated noticeable bactericidal ability of the GO-Ag hybrid system. We provide more chemo-physical evidence explaining the antibacterial behavior of GO-Ag nanohybrid against Gram-negative Escherichia Coli and Gram-positive Staphylococcus aureus in light of ultrastructural damage analyses and Ag1+ ions release rate onto the cells/medium. A further understanding of the mode of antimicrobial action is very important for designing and developing advanced antimicrobial systems. Secondly, we have also demonstrated that the GO-Ag nanohybrid material could be used as a potential surface enhanced Raman scattering (SERS) substrate to detect and quantify organic dyes, e.g., methylene blue (MB), in aqueous media. Our findings revealed that the GO-Ag hybrid system showed better SERS performance of MB detection than that of pure Ag-NPs. MB could be detected at a concentration as low as 1 ppm. The GO-Ag-based SERS platform can be effectively used to detect trace concentrations of various types of organic dyes in aqueous media. With the aforementioned properties, the GO-Ag hybrid system is found to be very promising as a multi-functional material for advanced biomedicine and environmental monitoring applications.

  12. Preparation of C60(O)n-ZnO nanocomposite under electric furnace and photocatalytic degradation of organic dyes.

    PubMed

    Cho, Bum Hwi; Oh, Youn Jun; Mun, Sang Mi; Ko, Weon Bae

    2012-07-01

    Zinc oxide (ZnO) nanoparticles were synthesized sonochemically by applying ultrasonic irradiation to a mixed aqueous-alcoholic solution of zinc nitrate with sodium hydroxide at room temperature. The morphology and optical properties of the ZnO nanoparticles were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-vis spectroscopy. The C60(O)n nanoparticles were synthesized by heating a mixture of C60 and 3-chloroperoxybenzoic acid in a benzene solvent under the reflux system. The heated C60(O)n-ZnO nanocomposite was synthesized in an electric furnace at 700 degrees C for two hours. The heated C60(O)n-ZnO nanocomposite was characterized by XRD, SEM, and TEM, and examined as a catalyst in the photocatalytic degradation of organic dyes by UV-vis spectroscopy. The photocatalytic effect of the heated C60(O)n-ZnO nanocomposite was evaluated by a comparison with that of unheated C60(O)n nanoparticles, heated C60(O)n nanoparticles, and unheated C60(O)n-ZnO in organic dyes, such as methylene blue (MB), methyl orange (MO), and rhodamine B (RhB) under ultraviolet light at 365 nm.

  13. Synthesis of [60]fullerene-ZnO nanocomposite under electric furnace and photocatalytic degradation of organic dyes.

    PubMed

    Hong, Sung Kyu; Lee, Jeong Ho; Ko, Weon Bae

    2011-07-01

    Zinc oxide (ZnO) nanoparticles were synthesized by a reaction between an aqueous-alcoholic solution of zinc nitrate and sodium hydroxide under ultrasonic irradiation at room temperature. The morphology, optical properties of the ZnO nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis spectroscopy. The [60]fullerene and zinc oxide nanocomposite were synthesized in an electric furnace at 700 degrees C for two hours. The [60]fullerene-ZnO nanocomposite was characterized by XRD, SEM and TEM. In addition, the [60]fullerene-ZnO nanocomposite was investigated as a catalyst in the photocatalytic degradation of organic dyes using UV-vis spectroscopy. The photocatalytic activity of the [60]fullerene-ZnO nanocomposite was compared with that of ZnO nanoparticles, heated ZnO nanoparticles after synthesis, pure [60]fullerene, and heated pure [60]fullerene in organic dyes such as methylene blue (MB), methyl orange (MO), and rhodamine B (RhB) under ultraviolet light at 254 nm.

  14. Adsorption and kinetic studies of seven different organic dyes onto magnetite nanoparticles loaded tea waste and removal of them from wastewater samples

    NASA Astrophysics Data System (ADS)

    Madrakian, Tayyebeh; Afkhami, Abbas; Ahmadi, Mazaher

    2012-12-01

    Adsorption of seven different organic dyes from aqueous solutions onto magnetite nanoparticles loaded tea waste (MNLTW) was studied. MNLTW was prepared via a simple method and was fully characterized. The properties of this magnetic adsorbent were characterized by scanning electron microscopy and X-ray diffraction. Adsorption characteristics of the MNLTW adsorbent was examined using Janus green, methylene blue, thionine, crystal violet, Congo red, neutral red and reactive blue 19 as adsorbates. Dyes adsorption process was thoroughly studied from both kinetic and equilibrium points of view for all adsorbents. The experimental isotherm data were analyzed using Langmuir, Freundlich, Sips, Redlich-Peterson, Brouers-Sotolongo and Temkin isotherms. The results from Langmuir isotherm indicated that the capacity of MNLTW for the adsorption of cationic dyes was higher than that for anionic dyes. The adsorption kinetics was tested for the pseudo-first order and pseudo-second order kinetic models at different experimental conditions.

  15. Stimulated resonance Raman scattering from organic dyes in a multiple-scattering medium as a potential method for determining their vibrational spectra

    SciTech Connect

    Yashchuk, V P; Tikhonov, E A; Bukatar', A O; Prigodiuk, O A; Smalyuk, A P

    2011-10-31

    A method is described for deriving Raman spectra of organic dyes from their random lasing spectra. The method was tested using Rhodamine 6G. The Raman spectrum obtained for this dye agrees well with the spectra measured by standard techniques but is more structured, which allows unresolved features to be detected. The spectrum provides more detailed information owing to the interference between the Raman scattered light and amplified spontaneous emission of the dye molecules within a photon mean free path. One advantage of the method is that the luminescence of the dye helps to observe Raman lines, which allows one to work in the Stokes region and facilitates the measurement procedure. (nonlinear optical phenomena)

  16. Adsorption and kinetic studies of seven different organic dyes onto magnetite nanoparticles loaded tea waste and removal of them from wastewater samples.

    PubMed

    Madrakian, Tayyebeh; Afkhami, Abbas; Ahmadi, Mazaher

    2012-12-01

    Adsorption of seven different organic dyes from aqueous solutions onto magnetite nanoparticles loaded tea waste (MNLTW) was studied. MNLTW was prepared via a simple method and was fully characterized. The properties of this magnetic adsorbent were characterized by scanning electron microscopy and X-ray diffraction. Adsorption characteristics of the MNLTW adsorbent was examined using Janus green, methylene blue, thionine, crystal violet, Congo red, neutral red and reactive blue 19 as adsorbates. Dyes adsorption process was thoroughly studied from both kinetic and equilibrium points of view for all adsorbents. The experimental isotherm data were analyzed using Langmuir, Freundlich, Sips, Redlich-Peterson, Brouers-Sotolongo and Temkin isotherms. The results from Langmuir isotherm indicated that the capacity of MNLTW for the adsorption of cationic dyes was higher than that for anionic dyes. The adsorption kinetics was tested for the pseudo-first order and pseudo-second order kinetic models at different experimental conditions. PMID:23058993

  17. Variation in the concentration of carminic acid produced by Dactylopius coccus (Hemiptera: Dactylopidae) at various maturation stages.

    PubMed

    Flores-Alatorre, H L; Abrego-Reyes, V; Reyes-Esparza, J A; Angeles, E; Alba-Hurtado, F

    2014-08-01

    The concentration of carminic acid was found to vary based on the size and life cycle stage of the cochineal, Dactylopius coccus Costa. The concentration of carminic acid in cochineal eggs, nymph I, nymph II, fertilized adults, ovipositing adults, and sterile adults female was measured using capillary electrophoresis, and the total fluorescence of the carminic acid globules was measured using flow cytometry. The smallest sterile adult females had a greater percentage of carminic acid relative to their weight (26.27%; P < 0.001) than adult females in the remaining groups. In general, ovipositing females had a greater percentage of carminic acid than the remainder of the females. Nymph II was the phase that had the smallest percentage of carminic acid. Using flow cytometry, it was demonstrated that ovipositing females had a greater total fluorescence than the other sampled groups (P < 0.05). A positive correlation was found between the percentage of carminic acid and the total fluorescence of the carminic acid globules (r2 = 0.68; P < 0.05). The results of this study, together with others that involve industrial processes, shall allow an improvement of the current classification criteria of the commercial quality of dry cochineal. PMID:25195465

  18. Smectite clays of Serbia and their application in adsorption of organic dyes

    NASA Astrophysics Data System (ADS)

    Milošević, Maja; Logar, Mihovil

    2014-05-01

    Colorants and dyes are currently available in over a 100.000 different species and several biggest industries are using them daily in their manufacture processes (textile, cosmetics, food industry, etc.). Since colorants are easily dissoluble in water they pass through filter membranes without further decomposing and in that manner they end up in the environment. The main goal of this work is to apply certain methods in determining the suitability of individual clay in adsorbing and removing colorants from polluted waters. For this study we have chosen four different raw clays from three regions in Serbia: Svrljig (B), Bogovina (Bo) and Slatina-Ub (C and V) and as colorant - methylene blue dye (MB (MERCK, for analytical purposes)). Experiments where carried out to determine the sample structure (XRD and IR), grain size (granulometry), cationic exchange capacity (CEC via spectrophotometry using MB) and adsorption capabilities (spectrophotometry and fluorimetry using MB). XRD and IR data are showing that the samples are smectite clays where samples B i Bo are mainly montmorillonite while C and V are montmorillonite-illite clays. Granulometric distribution results indicate that samples B i Bo have smaller grain size, less that 1μ (over 60%) whereas the samples C and V are more coarse grained (40% over 20μ). This grain distribution is affecting their specific surface area in the manner that those coarse grained samples have smaller specific surface area. Cationic exchange capacity determined with methylene blue indicate that montmorillonite samples have larger CEC (B = 37 meq/100g, Bo = 50 meq/100g) and montmorillonite-illite samples smaller CEC (V = 5 meq/100g, V = 3 meq/100g). Fluorimetry measurement results gave us a clear distinction between those with higher and smaller adsorption capability. Montmorillonite samples (B and Bo) with higher CEC values and smaller grain size are adsorbing large amounts of methylene blue witch is visible by absence of fluorimetric

  19. [Identification of acid-stable carmine in imported apple syrup product].

    PubMed

    Kawasaki, Yoko; Sugimoto, Naoki; Sato, Kyoko; Yamazaki, Takeshi; Ishiwata, Hajimu; Maitani, Tamio

    2002-08-01

    An unknown red pigment was purified from an apple syrup product imported from Canada, using a DIAION HP-20 column with methanol as the eluent. By spectroscopic means and chemical synthesis, the isolated pigment was identified as 4-aminocarminic acid, which is the major pigment of acid-stable carmine (a red colorant illegal in Japan). In addition, HPLC and TLC methods were proposed to detect this illegal colorant. While the color of carminic acid changed from yellow to red in the pH range of McIlvaine buffer (3.0-7.0), the color of 4-aminocarminic acid was always red, and also the ultraviolet/visible (UV/Vis) spectra did not change. These characteristics are useful to distinguish 4-aminocarminic acid from carminic acid. PMID:12436709

  20. Genotoxicity studies in vitro and in vivo on carminic acid (natural red 4).

    PubMed

    Loprieno, G; Boncristiani, G; Loprieno, N

    1992-09-01

    The potential genotoxic activity of carminic acid (CAS no. 1260-17-9; EINECS no. 215-023-3; C.I. no. 75410), a component of natural red colouring products (cochineal: CAS no. 1343-78-8; EINECS no. 215-680-6; C.I. no. 75470), used in food, cosmetics and drugs, has been evaluated by means of a series of short-term tests in vitro and in vivo, namely Salmonella reverse mutation, chromosome aberrations and sister chromatid exchanges in vitro on Chinese hamster ovary cells, and the mouse micronucleus test. All studies have produced negative results. The data obtained strongly support the non-mutagenic/non-carcinogenic activity of this compound. Genotoxicity data previously obtained for carminic acid, concerning the induction of a series of other genetic endpoints in different test systems, have also been considered, as have recent findings that indicate lack of carcinogenic activity in the cochineal preparation containing 29.8% carminic acid. PMID:1385283

  1. Defensive use of an acquired substance (carminic acid) by predaceous insect larvae.

    PubMed

    Eisner, T; Ziegler, R; McCormick, J L; Eisner, M; Hoebeke, E R; Meinwald, J

    1994-06-15

    Larvae of two insects, a coccinellid beetle (Hyperaspis trifurcata) and a chamaemyiid fly (Leucopis sp.), feed on cochineal insects and appropriate their prey's defensive chemical, carminic acid, for protective purposes of their own. H. trifurcata discharges the chemical with droplets of blood (hemolymph) that it emits when disturbed; Leucopis sp. ejects the compound with rectal fluid. Ants are thwarted by these defenses, which are compared with the previously-described defense of a pyralid caterpillar (Laetilia coccidivora) that disgorges carminic acid-laden crop fluid. The defensive fluid of all three larvae contains carminic acid at concentrations spanning a range (0.2-6.2%) proven deterrent to ants. Many insects are known to appropriate defensive substances from plants. Insects that acquire defensive chemicals from animal sources may be relatively rare. PMID:8020623

  2. Chromatographic and spectroscopic identification and recognition of ammoniacal cochineal dyes and pigments

    NASA Astrophysics Data System (ADS)

    Chieli, A.; Sanyova, J.; Doherty, B.; Brunetti, B. G.; Miliani, C.

    2016-06-01

    In this work a combined chromatographic and spectroscopic approach is used to provide a diagnostic assessment of semi-synthetic ammoniacal cochineal through the syntheses of its dyes and lakes according to art historical recipes. Commercially introduced in the late XIX century as a dye and pigment, it was used to obtain a brilliant purplish/violet nuance which provided a more stable option over carminic acid although its evidenced use in manufacts and artworks of heritage importance have been scarcely documented. Through HPLC-DAD, it has been possible to identify 4-aminocarminic acid as the main component of ammoniacal cochineal highlighting a chemical formula analogous to acid stable carmine, a recent patented food dye. FTIR clearly distinguishes the amine group in the ammoniacal cochineal dye preparation and TLC-SERS allows for an adequate separation and spectral differentiation in its main components to be evidenced. Colloidal SERS has permitted spectral markers useful in discerning ammoniacal cochineal over carminic acid to be highlighted and discussed. Finally, the methods experimented in this study for the identification of ammoniacal cochineal have been validated on analyzing a sample of dyed wool.

  3. Chromatographic and spectroscopic identification and recognition of ammoniacal cochineal dyes and pigments.

    PubMed

    Chieli, A; Sanyova, J; Doherty, B; Brunetti, B G; Miliani, C

    2016-06-01

    In this work a combined chromatographic and spectroscopic approach is used to provide a diagnostic assessment of semi-synthetic ammoniacal cochineal through the syntheses of its dyes and lakes according to art historical recipes. Commercially introduced in the late XIX century as a dye and pigment, it was used to obtain a brilliant purplish/violet nuance which provided a more stable option over carminic acid although its evidenced use in manufacts and artworks of heritage importance have been scarcely documented. Through HPLC-DAD, it has been possible to identify 4-aminocarminic acid as the main component of ammoniacal cochineal highlighting a chemical formula analogous to acid stable carmine, a recent patented food dye. FTIR clearly distinguishes the amine group in the ammoniacal cochineal dye preparation and TLC-SERS allows for an adequate separation and spectral differentiation in its main components to be evidenced. Colloidal SERS has permitted spectral markers useful in discerning ammoniacal cochineal over carminic acid to be highlighted and discussed. Finally, the methods experimented in this study for the identification of ammoniacal cochineal have been validated on analyzing a sample of dyed wool. PMID:26985877

  4. Experimental and numerical investigation of the effect of liquid temperature on the sonolytic degradation of some organic dyes in water.

    PubMed

    Merouani, Slimane; Hamdaoui, Oualid; Boutamine, Zineb; Rezgui, Yacine; Guemini, Miloud

    2016-01-01

    This paper presents a comprehensive experimental and numerical investigation of the effects of liquid temperature on the sonochemical degradation of three organic dyes, Rhodamine B (RhB), Acid orange 7 (AO7) and Malachite green (MG), largely used in the textile industry. The experiments have been carried out for an ultrasonic frequency of 300 kHz. The obtained experimental results were discussed using a new approach combining the results of single-bubble event and the number of active bubbles. The single-bubble event was predicted using a model that combines the bubble dynamics with chemical kinetics occurring inside a bubble during the strong collapse. The number of active bubbles was predicted using a method developed in our previous work. The experiments showed that the degradation rate of the three dyes increased significantly with increasing liquid temperature in the range 25-55°C. It was predicted that the main pathway of pollutants degradation is the attack by OH radicals. The simulations showed that there exists an optimum liquid temperature of about 35°C for the production of OH inside a bubble whereas the number of active bubbles increased sharply with the rise of the liquid temperature. It was predicted that the overall production rate of OH increased with increasing liquid temperature in the range 25-55°C. Finally, it was concluded that the effect of liquid temperature on the sonochemical degradation of the three dyes in aqueous phase was controlled by the number of active bubbles in the range 35-55°C and by both the number of bubbles and the single bubble yield in the range 25-35°C. PMID:26384922

  5. Experimental and numerical investigation of the effect of liquid temperature on the sonolytic degradation of some organic dyes in water.

    PubMed

    Merouani, Slimane; Hamdaoui, Oualid; Boutamine, Zineb; Rezgui, Yacine; Guemini, Miloud

    2016-01-01

    This paper presents a comprehensive experimental and numerical investigation of the effects of liquid temperature on the sonochemical degradation of three organic dyes, Rhodamine B (RhB), Acid orange 7 (AO7) and Malachite green (MG), largely used in the textile industry. The experiments have been carried out for an ultrasonic frequency of 300 kHz. The obtained experimental results were discussed using a new approach combining the results of single-bubble event and the number of active bubbles. The single-bubble event was predicted using a model that combines the bubble dynamics with chemical kinetics occurring inside a bubble during the strong collapse. The number of active bubbles was predicted using a method developed in our previous work. The experiments showed that the degradation rate of the three dyes increased significantly with increasing liquid temperature in the range 25-55°C. It was predicted that the main pathway of pollutants degradation is the attack by OH radicals. The simulations showed that there exists an optimum liquid temperature of about 35°C for the production of OH inside a bubble whereas the number of active bubbles increased sharply with the rise of the liquid temperature. It was predicted that the overall production rate of OH increased with increasing liquid temperature in the range 25-55°C. Finally, it was concluded that the effect of liquid temperature on the sonochemical degradation of the three dyes in aqueous phase was controlled by the number of active bubbles in the range 35-55°C and by both the number of bubbles and the single bubble yield in the range 25-35°C.

  6. Electroactive organic dye incorporating dipeptides in the formation of self-assembled nanofibrous hydrogels.

    PubMed

    Liu, Yu-Hao; Hsu, Shu-Min; Wu, Fang-Yi; Cheng, Hsun; Yeh, Mei-Yu; Lin, Hsin-Chieh

    2014-10-15

    In this study, we examined the self-assembly of four dipeptides conjugated with the electroactive dye naphthalenediimide (NDI). The presence of the NDI group at the N-terminus of Phe-Phe and Phe-Gly promoted the formation of one-dimensional (1-D) nanostructures and three-dimensional (3-D) colored hydrogels under both acidic and physiological conditions. The 1-D nanostructures of these gels were stabilized through intermolecular π-π interactions of the conjugated systems and extended hydrogen bonding of the dipeptide units. PMID:25229206

  7. UV light induced photodegradation of organic dye by ZnO nanocatalysts

    SciTech Connect

    Sumesh, C. K.; Patel, Bhavin; Parekh, Kinnari

    2013-06-03

    Ultraviolet light induced photocatalytic activity of ZnO nanocatalyst prepared using a wet chemical precipitation route and mineralization of the methyl orange (MO) dye has been carried out in a photocatalytic reactor. The degradation of the MO was monitored spectrophotometrically and showed a decolorization efficiency of 92% after nine hours of irradiation in the MO-ZnO/UV light system. The blue shifting of maximum peak position of the MO and the formation of extra peak at 247 nm during irradiation time advances revealed that MO degrades in the form of intermediates during the photocatalytic process.

  8. Synthesis of organic photosensitizers containing dithienogermole and thiadiazolo[3,4-c]pyridine units for dye-sensitized solar cells.

    PubMed

    Adachi, Yohei; Ooyama, Yousuke; Shibayama, Naoyuki; Ohshita, Joji

    2016-09-21

    Dithienogermole (DTG) is a germanium-bridged bithiophene system that has been applied as a building unit of conjugated materials for organic electronic devices, including organic photovoltaics and organic light emitting diodes. However, DTG has not been used as a component of sensitizers for dye-sensitized solar cells (DSSCs). In this work, we have synthesized three D-π-A-π-A type sensitizers containing DTG and thiadiazolo[3,4-c]pyridine (PTz). We expected that combining DTG and a strong acceptor PTz would give rise to a strong absorption in the visible region. In addition, we introduced bulky 2-ethylhexyl groups on the germanium atom to prevent dye aggregation on TiO2 films. Three DTG-containing dyes with different anchor units were synthesized and their optical/electrochemical properties were investigated. The DTG-containing dyes exhibited broad and strong absorption bands around 600 nm on TiO2. We fabricated DSSCs based on the DTG-containing dyes. The onsets of incident photon to current conversion efficiency (IPCE) spectra reached 900 nm and a maximal power conversion efficiency of 2.76% was achieved.

  9. Synthesis of organic photosensitizers containing dithienogermole and thiadiazolo[3,4-c]pyridine units for dye-sensitized solar cells.

    PubMed

    Adachi, Yohei; Ooyama, Yousuke; Shibayama, Naoyuki; Ohshita, Joji

    2016-09-21

    Dithienogermole (DTG) is a germanium-bridged bithiophene system that has been applied as a building unit of conjugated materials for organic electronic devices, including organic photovoltaics and organic light emitting diodes. However, DTG has not been used as a component of sensitizers for dye-sensitized solar cells (DSSCs). In this work, we have synthesized three D-π-A-π-A type sensitizers containing DTG and thiadiazolo[3,4-c]pyridine (PTz). We expected that combining DTG and a strong acceptor PTz would give rise to a strong absorption in the visible region. In addition, we introduced bulky 2-ethylhexyl groups on the germanium atom to prevent dye aggregation on TiO2 films. Three DTG-containing dyes with different anchor units were synthesized and their optical/electrochemical properties were investigated. The DTG-containing dyes exhibited broad and strong absorption bands around 600 nm on TiO2. We fabricated DSSCs based on the DTG-containing dyes. The onsets of incident photon to current conversion efficiency (IPCE) spectra reached 900 nm and a maximal power conversion efficiency of 2.76% was achieved. PMID:27510746

  10. Influence of niobium doping in hierarchically organized titania nanostructure on performance of dye-sensitized solar cells.

    PubMed

    Park, Jong Hoon; Noh, Jun Hong; Han, Byung Suh; Shin, Seong Sik; Park, Ik Jae; Kim, Dong Hoe; Hong, Kug Sun

    2012-06-01

    Niobium doped hierarchically organized TiO2 nanostructures composed of 20 nm size anatase nanocrystals were synthesized using pulsed laser deposition (PLD). The Nb doping concentration could be facilely controlled by adjusting the concentration of Nb in target materials. We could investigate the influence of Nb doping in the TiO2 photoelectrode on the cell performance of dye-sensitized solar cells (DSSCs) by the exclusion of morphological effects using the prepared Nb-doped TiO2 anostructures. We found no significant change in short circuit current density (Jsc) as a function of Nb doping concentration. However, open circuit voltage (Voc) and fill factor (FF) monotonously decrease with increasing Nb concentration. Dark current characteristics of the DSSCs reveal that the decrease in Voc and FF is attributed to the decrease in shunt resistance due to the increase in conductivity TiO2 by Nb doping. However, electrochemical impedance spectra (EIS) analysis at open circuit condition under illumination showed that the resistance at the TiO2/dye/electrolyte interface increases with Nb concentration, revealing that Nb doping suppress the charge recombination at the interface. In addition, electron life time obtained using characteristic frequency in Bode plot increases from 14 msec to 56 msec with increasing Nb concentration from 0 to 1.2 at%. This implies that the improved light harvesting can be achieved by increasing diffusion length through Nb-doping in the conventional TiO2 photoelectrode.

  11. Facile and Scalable Preparation of Graphene Oxide-Based Magnetic Hybrids for Fast and Highly Efficient Removal of Organic Dyes

    NASA Astrophysics Data System (ADS)

    Jiao, Tifeng; Liu, Yazhou; Wu, Yitian; Zhang, Qingrui; Yan, Xuehai; Gao, Faming; Bauer, Adam J. P.; Liu, Jianzhao; Zeng, Tingying; Li, Bingbing

    2015-07-01

    This study reports the facile preparation and the dye removal efficiency of nanohybrids composed of graphene oxide (GO) and Fe3O4 nanoparticles with various geometrical structures. In comparison to previously reported GO/Fe3O4 composites prepared through the one-pot, in situ deposition of Fe3O4 nanoparticles, the GO/Fe3O4 nanohybrids reported here were obtained by taking advantage of the physical affinities between sulfonated GO and Fe3O4 nanoparticles, which allows tuning the dimensions and geometries of Fe3O4 nanoparticles in order to decrease their contact area with GO, while still maintaining the magnetic properties of the nanohybrids for easy separation and adsorbent recycling. Both the as-prepared and regenerated nanohybrids demonstrate a nearly 100% removal rate for methylene blue and an impressively high removal rate for Rhodamine B. This study provides new insights into the facile and controllable industrial scale fabrication of safe and highly efficient GO-based adsorbents for dye or other organic pollutants in a wide range of environmental-related applications.

  12. Hybrid functional calculated optical and electronic structures of thin anatase TiO2 nanowires with organic dye adsorbates

    NASA Astrophysics Data System (ADS)

    Ünal, Hatice; Gunceler, Deniz; Gülseren, Oğuz; Ellialtıoğlu, Şinasi; Mete, Ersen

    2015-11-01

    The electronic and optical properties of thin anatase TiO2 (1 0 1) and (0 0 1) nanowires have been investigated using the screened Coulomb hybrid density functional calculations. For the bare nanowires with sub-nanometer diameters, the calculated band gaps are larger relative to the bulk values due to size effects. The role of organic light harvesting sensitizers on the absorption characteristics of the anatase nanowires has been examined using the hybrid density functional method incorporating partial exact exchange with range separation. For the lowest lying excitations, directional charge redistribution of tetrahydroquinoline (C2-1) dye shows a remarkably different profile in comparison to a simple molecule which is chosen as the coumarin skeleton. The binding modes and the adsorption energies of C2-1 dye and coumarin core on the anatase nanowires have been studied including non-linear solvation effetcs. The calculated optical and electronic properties of the nanowires with these two different types of sensitizers have been interpreted in terms of their electron-hole generation, charge carrier injection and recombination characteristics.

  13. Tunable synthesis of SiO2-encapsulated zero-valent iron nanoparticles for degradation of organic dyes

    PubMed Central

    2014-01-01

    A series of nanocomposites consisting of zero-valent iron nanoparticles (ZVI NPs) encapsulated in SiO2 microspheres were successfully synthesized through a successive two-step method, i.e., the wet chemical reduction by borohydride followed by a modified Stöber method. The as-synthesized nanocomposites were characterized using X-ray diffraction, field emission scanning electron microscopy, vibrating sample magnetometer, and inductively coupled plasma-atomic emission spectrometer. The catalytic performance of SiO2-encapsulated ZVI nanocomposites for the degradation of organic dyes was investigated using methylene blue (MB) as the model dye in the presence of H2O2. The results showed that the degradation efficiency and apparent rate constant of the degradation reaction were significantly enhanced with increased ZVI NPs encapsulated in SiO2 microspheres, whereas the dosage of H2O2 remarkably promoted degradation rate without affecting degradation efficiency. The content-dependent magnetic property ensured the excellent magnetic separation of degradation products under an external magnet. This strategy for the synthesis of SiO2-encapsulated ZVI NPs nanocomposites was low cost and easy to scale-up for industrial production, thereby enabling promising applications in environmental remediation. PMID:25258615

  14. Facile and Scalable Preparation of Graphene Oxide-Based Magnetic Hybrids for Fast and Highly Efficient Removal of Organic Dyes

    PubMed Central

    Jiao, Tifeng; Liu, Yazhou; Wu, Yitian; Zhang, Qingrui; Yan, Xuehai; Gao, Faming; Bauer, Adam J. P.; Liu, Jianzhao; Zeng, Tingying; Li, Bingbing

    2015-01-01

    This study reports the facile preparation and the dye removal efficiency of nanohybrids composed of graphene oxide (GO) and Fe3O4 nanoparticles with various geometrical structures. In comparison to previously reported GO/Fe3O4 composites prepared through the one-pot, in situ deposition of Fe3O4 nanoparticles, the GO/Fe3O4 nanohybrids reported here were obtained by taking advantage of the physical affinities between sulfonated GO and Fe3O4 nanoparticles, which allows tuning the dimensions and geometries of Fe3O4 nanoparticles in order to decrease their contact area with GO, while still maintaining the magnetic properties of the nanohybrids for easy separation and adsorbent recycling. Both the as-prepared and regenerated nanohybrids demonstrate a nearly 100% removal rate for methylene blue and an impressively high removal rate for Rhodamine B. This study provides new insights into the facile and controllable industrial scale fabrication of safe and highly efficient GO-based adsorbents for dye or other organic pollutants in a wide range of environmental-related applications. PMID:26220847

  15. Hydrothermal fabrication of selectively doped organic assisted advanced ZnO nanomaterial for solar driven photocatalysis.

    PubMed

    Namratha, K; Byrappa, K; Byrappa, S; Venkateswarlu, P; Rajasekhar, D; Deepthi, B K

    2015-08-01

    Hydrothermal fabrication of selectively doped (Ag(+)+Pd(3+)) advanced ZnO nanomaterial has been carried out under mild pressure temperature conditions (autogeneous; 150°C). Gluconic acid has been used as a surface modifier to effectively control the particle size and morphology of these ZnO nanoparticles. The experimental parameters were tuned to achieve optimum conditions for the synthesis of selectively doped ZnO nanomaterials with an experimental duration of 4 hr. These selectively doped ZnO nanoparticles were characterized using powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-Vis spectroscopy and scanning electron microscopy (SEM). The solar driven photocatalytic studies have been carried out for organic dyes, i.e., Procion MX-5B dye, Cibacron Brilliant Yellow dye, Indigo Carmine dye, separately and all three mixed, by using gluconic acid modified selectively doped advanced ZnO nanomaterial. The influence of catalyst, its concentration and initial dye concentration resulted in the photocatalytic efficiency of 89% under daylight.

  16. Organic Dyes Incorporating the Dithieno[3,2-f:2',3'-h]quinoxaline Moiety for Dye-Sensitized Solar Cells.

    PubMed

    Ni, Jen-Shyang; Kao, Wei-Siang; Chou, Hao-Ju; Lin, Jiann T

    2015-09-01

    New donor-acceptor'-acceptor-type sensitizers (QBT dyes), comprising arylamine as the electron donor, dithieno[3,2-f:2',3'-h]quinoxaline as the internal acceptor, and 2-cyanoacrylic acid as both the acceptor and anchor, have been synthesized. The QBT dyes have broad absorption spectra covering the range of λ=368-487 nm with a highest molar extinction coefficient of up to approximately 40 000 M(-1)  cm(-1) . The light-to-electricity conversion efficiencies of the dye-sensitized solar cells (DSSCs) fabricated from the dyes range from 6.11 to 7.59 % under simulated AM 1.5 G illumination. Upon addition of a threefold concentration of chenodeoxycholic acid as the co-adsorbent, the best performance cell has a power-conversion efficiency of 8.41 %, which is higher than that of the N719-based standard DSSC (8.27 %).

  17. An organic redox electrolyte to rival triiodide/iodide in dye-sensitized solar cells.

    PubMed

    Wang, Mingkui; Chamberland, Nathalie; Breau, Livain; Moser, Jacques-E; Humphry-Baker, Robin; Marsan, Benoît; Zakeeruddin, Shaik M; Grätzel, Michael

    2010-05-01

    Dye-sensitized solar cells (DSCs) have achieved impressive conversion efficiencies for solar energy of over 11% with an electrolyte that contains triiodide/iodide as a redox couple. Although triiodide/iodide redox couples work efficiently in DSCs, they suffer from two major disadvantages: electrolytes that contain triiodide/iodide corrode electrical contacts made of silver (which reduces the options for the scale up of DSCs to module size) and triiodide partially absorbs visible light. Here, we present a new disulfide/thiolate redox couple that has negligible absorption in the visible spectral range, a very attractive feature for flexible DSCs that use transparent conductors as current collectors. Using this novel, iodide-free redox electrolyte in conjunction with a sensitized heterojunction, we achieved an unprecedented efficiency of 6.4% under standard illumination test conditions. This novel redox couple offers a viable pathway to develop efficient DSCs with attractive properties for scale up and practical applications.

  18. Room temperature synthesis of a Zn(II) metal-organic coordination polymer for dye removal

    NASA Astrophysics Data System (ADS)

    Abbasi, Alireza; Gharib, Maniya; Najafi, Mahnaz; Janczak, Jan

    2016-03-01

    A new one-dimensional (1D) coordination polymer, [Zn(4,4‧-bpy)(H2O)4](ADC)·4H2O (1) (4,4‧-bpy=4,4‧-bipyridine and H2ADC=acetylenedicarboxylic acid), was synthesized at room temperature. The crystal structure of the coordination polymer was determined by single-crystal X-ray diffraction analysis. Compound 1 was also characterized by FT-IR, powder X-ray diffraction (PXRD) and thermogravimetric analysis (TGA). The catalytic activity of 1 was evaluated in the color removal of Bismarck brown as a representative of dye pollutant in water under mild conditions. Coordination polymer 1 exhibited good catalytic activity and stability in the decolorization of Bismarck brown and could be easily recovered and reused for at least three cycles.

  19. Aqueous synthesis of hierarchical bismuth nanobundles with high catalytic activity to organic dyes

    NASA Astrophysics Data System (ADS)

    Ma, Dechong; Zhao, Yan; Zhao, Jingzhe; Li, Yawen; Lu, Yan; Zhao, Duijia

    2015-07-01

    Bundle-like bismuth (Bi) nanoarchitectures were successfully prepared on a large scale by an aqueous reducing strategy with polyethylene glycol (PEG) as directing agent at 90 °C for 55 min. The bundle-like Bi nanoarchitectures have a length of 4-5 μm and diameter of 0.5-1 μm with fairly uniform construction. Catalytic activities of the as-prepared hierarchical Bi nanobundles were investigated for degrading Rhodamine B (RhB) dye solution under visible-light irradiation. The Bi nanostructures extended excellent catalytic activity and good cycling performance toward photodegradation of RhB. Possible mechanism was proposed for Bi-assisted photocatalytic degradation of RhB under visible-light.

  20. Metal-free organic sensitizers for use in water-splitting dye-sensitized photoelectrochemical cells

    PubMed Central

    Swierk, John R.; Méndez-Hernández, Dalvin D.; McCool, Nicholas S.; Liddell, Paul; Terazono, Yuichi; Pahk, Ian; Tomlin, John J.; Oster, Nolan V.; Moore, Thomas A.; Moore, Ana L.; Gust, Devens; Mallouk, Thomas E.

    2015-01-01

    Solar fuel generation requires the efficient capture and conversion of visible light. In both natural and artificial systems, molecular sensitizers can be tuned to capture, convert, and transfer visible light energy. We demonstrate that a series of metal-free porphyrins can drive photoelectrochemical water splitting under broadband and red light (λ > 590 nm) illumination in a dye-sensitized TiO2 solar cell. We report the synthesis, spectral, and electrochemical properties of the sensitizers. Despite slow recombination of photoinjected electrons with oxidized porphyrins, photocurrents are low because of low injection yields and slow electron self-exchange between oxidized porphyrins. The free-base porphyrins are stable under conditions of water photoelectrolysis and in some cases photovoltages in excess of 1 V are observed. PMID:25583488

  1. Separation and recovery of food coloring dyes using aqueous biphasic extraction chromatographic resins.

    PubMed

    Huddleston, J G; Willauer, H D; Boaz, K R; Rogers, R D

    1998-06-26

    Aqueous biphasic systems (ABS) and aqueous biphasic extraction chromatographic (ABEC) resins are currently under investigation for their utility in the removal of color from textile plant wastes. The structures of several widely used food colorings, suggest that these dyes would also be retained on the resins. In work currently in progress, we have begun to investigate the retention and resolution of several common food colorings including indigo carmine, amaranth, carminic acid. erythrosin B, tartrazine and quinoline yellow. The relationship between the uptake of these dyes on ABEC resins in terms of the binding strengths and capacities of the resins and their partitioning behavior in ABS is illustrated. Some possible theoretical and practical approaches to the prediction of the partitioning and retention behavior is discussed. PMID:9699992

  2. Template-free synthesis of ZnV 2O 4 hollow spheres and their application for organic dye removal

    NASA Astrophysics Data System (ADS)

    Duan, Fang; Dong, Weifu; Shi, Dongjian; Chen, Mingqing

    2011-10-01

    Hollow ZnV 2O 4 spheres with the shell aggregated by small nanoparticles were successfully synthesized through a facile one-pot template-free solvothermal method. The as-prepared product was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), and Brunauer-Emmett-Teller N 2 adsorption-desorption analyses. The formation of ZnV 2O 4 hollow spheres was based on flowerlike intermediate products supported reduction-dissolution-aggregation process at the expense of consumption of all the flowerlike products. The obtained ZnV 2O 4 hollow spheres showed a good adsorption capacity of methylene blue (MB) organic dye, which might be attributed to their special structural feature with large surface area. The adsorption kinetics and isotherm of MB on ZnV 2O 4 hollow spheres were also studied.

  3. Recycling of agricultural solid waste, coir pith: removal of anions, heavy metals, organics and dyes from water by adsorption onto ZnCl2 activated coir pith carbon.

    PubMed

    Namasivayam, C; Sangeetha, D

    2006-07-31

    The abundant lignocellulosic agricultural waste, coir pith is used to develop ZnCl(2) activated carbon and applied to the removal of toxic anions, heavy metals, organic compounds and dyes from water. Sorption of inorganic anions such as nitrate, thiocyanate, selenite, chromium(VI), vanadium(V), sulfate, molybdate, phosphate and heavy metals such as nickel(II) and mercury(II) has been studied. Removal of organics such as resorcinol, 4-nitrophenol, catechol, bisphenol A, 2-aminophenol, quinol, O-cresol, phenol and 2-chlorophenol has also been investigated. Uptake of acidic dyes such as acid brilliant blue, acid violet, basic dyes such as methylene blue, rhodamine B, direct dyes such as direct red 12B, congo red and reactive dyes such as procion red, procion orange were also examined to assess the possible use of the adsorbent for the treatment of contaminated ground water. Favorable conditions for maximum removal of all adsorbates at the adsorbate concentration of 20 mg/L were used. Results show that ZnCl(2) activated coir pith carbon is effective for the removal of toxic pollutants from water.

  4. Recycling of agricultural solid waste, coir pith: removal of anions, heavy metals, organics and dyes from water by adsorption onto ZnCl2 activated coir pith carbon.

    PubMed

    Namasivayam, C; Sangeetha, D

    2006-07-31

    The abundant lignocellulosic agricultural waste, coir pith is used to develop ZnCl(2) activated carbon and applied to the removal of toxic anions, heavy metals, organic compounds and dyes from water. Sorption of inorganic anions such as nitrate, thiocyanate, selenite, chromium(VI), vanadium(V), sulfate, molybdate, phosphate and heavy metals such as nickel(II) and mercury(II) has been studied. Removal of organics such as resorcinol, 4-nitrophenol, catechol, bisphenol A, 2-aminophenol, quinol, O-cresol, phenol and 2-chlorophenol has also been investigated. Uptake of acidic dyes such as acid brilliant blue, acid violet, basic dyes such as methylene blue, rhodamine B, direct dyes such as direct red 12B, congo red and reactive dyes such as procion red, procion orange were also examined to assess the possible use of the adsorbent for the treatment of contaminated ground water. Favorable conditions for maximum removal of all adsorbates at the adsorbate concentration of 20 mg/L were used. Results show that ZnCl(2) activated coir pith carbon is effective for the removal of toxic pollutants from water. PMID:16406295

  5. An anionic zeolite-like metal-organic framework (AZMOF) with a Moravia network for organic dye absorption through cation-exchange.

    PubMed

    Shen, Yu; Fan, Cong-Cong; Wei, Yu-Zhen; Du, Jie; Zhu, Hai-Bin; Zhao, Yue

    2016-07-01

    An anionic zeolite-like metal-organic framework (AZMOF) with a twisted partially augmented the net, known as the "Moravia" net, [(CH3)2NH2]6[Sr13(O)3()8(OH)2(H2O)16]·xS (, where S represents non-coordinated solvent molecules, and is the abbreviation of benzo-(1,2;3,4;5,6)-tris-(thiophene-2'-carboxylic acid)), has been solvothermally synthesized and characterized, which possesses an anionic framework and nano-sized sodalite cage. Through cation-exchange, is capable of uptaking large organic cationic dyes including Rhodamine B (RB), Basic Red 2 (BR2), Crystal Violet (CV) and Methylene Blue (MB), amongst which the adsorption capability for RB (up to 545 mg g(-1)), and BR2 (up to 675 mg g(-1)) is the highest for reported absorbants to date. PMID:27301344

  6. The energy transfer mechanism of a photoexcited and electroluminescent organic hybrid thin film of blue, green, and red laser dyes.

    PubMed

    Li, Weiling; Zhang, Jing; Zheng, Yanqiong; Chen, Guo; Cai, Miao; Wei, Bin

    2015-01-01

    Though optically pumped lasing has been realized for years, electrically pumped lasing has not yet been achieved in organic semiconductor devices. In order to make a better understanding of the laser mechanisms of the organic materials, we prepared organic thin films consisting of three efficient laser dyes of a blue emitter, 4″,4″'-N,N-diphenylamine-4,4'-diphenyl-1,1'-binaphthyl (BN), a green emitter, 1,4-bis[2-[4-[N,N-di(p-tolyl)amino] phenyl]vinyl]benzene (DSB), and a red emitter, 4-(dicyanomethylene)-2-t-butyl-6(1,1,7,7-tetramethyljulolidy-l-9-enyl)-4H-pyran (DCJTB) with different doping concentrations for the first time to investigate the cascade energy transfer process. The energy transfer schemes in the co-doped thin films in photoluminescence and electroluminescence have been investigated. The results indicated that the DSB molecules acted as a bridge to deliver energy more effectively from the host (BN) to the guest (DCJTB). Meanwhile, the maximum current efficiency (C E) and power efficiency (P E) of the organic light-emitting devices (OLEDs) with the emitting layer of lower doping concentration were 13.5 cd/A and 14.1 lm/W, respectively.

  7. Selective adsorption of cationic dyes from aqueous solution by polyoxometalate-based metal-organic framework composite

    NASA Astrophysics Data System (ADS)

    Liu, Xiaoxia; Gong, Wenpeng; Luo, Jing; Zou, Chentao; Yang, Yun; Yang, Shuijin

    2016-01-01

    A novel environmental friendly adsorbent H6P2W18O62/MOF-5 was synthesized by a simple one-step reaction under solvothermal conditions and characterized by XRD, FTIR, thermogravimetric analyses (TGA) and N2 adsorption-desorption isotherms. The removal rate of H6P2W18O62/MOF-5 was quite greater (85%) than that of MOF-5 (almost zero), showing that the adsorption performance of porous MOF-5 can be improved through the modification of H6P2W18O62. Further study revealed that H6P2W18O62/MOF-5 exhibited a fast adsorption rate and selective adsorption ability towards the cationic dyes in aqueous solution. The removal rate was up to 97% for cationic dyes methylene blue (MB) and 68% for rhodamine B(Rhb) within 10 min. However, anionicdye methyl orange(MO) can only reach to 10%. The influences including initial concentration, contact time, initial solution pH and temperature of MB adsorption onto H6P2W18O62/MOF-5 were investigated in detail. The kinetic study indicated that the adsorption of MB onto H6P2W18O62/MOF-5 followed the pseudo second-order model well. The isotherm obtained from experimental data fitted the Langmuir model, yielding maximum adsorption capacity of 51.81 mg/g. The thermodynamic parameters analysis illustrated that the MB adsorption onto H6P2W18O62 immobilized MOF-5 was spontaneous and endothermic process. Besides, these results implied that designing a novel material polyoxometalate-based metal-organic frameworks is great potential for removing cationic organic pollutants and even extended to improve other specific application.

  8. Amphiphilic block-graft copolymer templates for organized mesoporous TiO2 films in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Lim, Jung Yup; Lee, Chang Soo; Lee, Jung Min; Ahn, Joonmo; Cho, Hyung Hee; Kim, Jong Hak

    2016-01-01

    Amphiphilic block-graft copolymers composed of poly(styrene-b-butadiene-b-styrene) (SBS) backbone and poly(oxyethylene methacrylate) (POEM) side chains are synthesized and combined with hydrophilically preformed TiO2 (Pre-TiO2), which works as a structural binder as well as titania source. This results in the formation of crack free, 6-μm-thick, organized mesoporous TiO2 (OM-TiO2) films via one-step doctor-blading based on self-assembly of SBS-g-POEM as well as preferential interaction of POEM chains with Pre-TiO2. SBS-g-POEM with different numbers of ethylene oxide repeating units, SBS-g-POEM(500) and SBS-g-POEM(950), are used to form OM-TiO2(500) and OM-TiO2(950), respectively. The efficiencies of dye-sensitized solar cells (DSSCs) with a quasi-solid-state polymer electrolyte reach 5.7% and 5.8% at 100 mW/cm2 for OM-TiO2(500) and OM-TiO2(950), respectively. The surface area of OM-TiO2(950) was greater than that of OM-TiO2(500) but the light reflectance was lower in the former, which is responsible for similar efficiency. Both DSSCs exhibit much higher efficiency than one (4.8%) with randomly-organized particulate TiO2 (Ran-TiO2), which is attributed to the higher dye loading, reduced charge recombination and improved pore infiltration of OM-TiO2. When utilizing poly((1-(4-ethenylphenyl)methyl)-3-butyl-imidazolium iodide) (PEBII) and mesoporous TiO2 spheres as the solid electrolyte and the scattering layer, the efficiency increases up to 7.5%, one of the highest values for N719-based solid-state DSSCs.

  9. Multifunctional Three-Dimensional Europium Metal-Organic Framework for Luminescence Sensing of Benzaldehyde and Cu(2+) and Selective Capture of Dye Molecules.

    PubMed

    Du, Pei-Yao; Gu, Wen; Liu, Xin

    2016-08-15

    A multifunctional three-dimensional lanthanide metal-organic framework has been rationally constructed. Highly selective sensing of benzaldehyde and Cu(2+) ions makes it a potential bifunctional sensor. Also, it could serve as a good candidate material for the removal of dyes from effluents based on the size exclusion. PMID:27458756

  10. Evaluation of quantum dot immunofluorescence and a digital CMOS imaging system as an alternative to conventional organic fluorescence dyes and laser scanning for quantifying protein microarrays.

    PubMed

    Jain, Aarti; Taghavian, Omid; Vallejo, Derek; Dotsey, Emmanuel; Schwartz, Dan; Bell, Florian G; Greef, Chad; Davies, D Huw; Grudzien, Jennipher; Lee, Abraham P; Felgner, Philip L; Liang, Li

    2016-04-01

    Organic fluorescent dyes are widely used for the visualization of bound antibody in a variety of immunofluorescence assays. However, the detection equipment is often expensive, fragile, and hard to deploy widely. Quantum dots (Qdot) are nanocrystals made of semiconductor materials that emit light at different wavelengths according to the size of the crystal, with increased brightness and stability. Here, we have evaluated a small benchtop "personal" optical imager (ArrayCAM) developed for quantification of protein arrays probed by Qdot-based indirect immunofluorescence. The aim was to determine if the Qdot imager system provides equivalent data to the conventional organic dye-labeled antibody/laser scanner system. To do this, duplicate proteome microarrays of Vaccinia virus, Brucella melitensis and Plasmodium falciparum were probed with identical samples of immune sera, and IgG, IgA, and IgM profiles visualized using biotinylated secondary antibodies followed by a tertiary reagent of streptavidin coupled to either P3 (an organic cyanine dye typically used for microarrays) or Q800 (Qdot). The data show excellent correlation for all samples tested (R > 0.8) with no significant change of antibody reactivity profiles. We conclude that Qdot detection provides data equivalent to that obtained using conventional organic dye detection. The portable imager offers an economical, more robust, and deployable alternative to conventional laser array scanners. PMID:26842269

  11. Dithiafulvenyl unit as a new donor for high-efficiency dye-sensitized solar cells: synthesis and demonstration of a family of metal-free organic sensitizers.

    PubMed

    Guo, Kunpeng; Yan, Keyou; Lu, Xiaoqing; Qiu, Yongcai; Liu, Zhike; Sun, Jianwei; Yan, Feng; Guo, Wenyue; Yang, Shihe

    2012-05-01

    This work identifies the dithiafulvenyl unit as an excellent electron donor for constructing D-π-A-type metal-free organic sensitizers of dye-sensitized solar cells (DSCs). Synthesized and tested are three sensitizers all with this donor and a cyanoacrylic acid acceptor but differing in the phenyl (DTF-C1), biphenyl (DTF-C2), and phenyl-thiopheneyl-phenyl π-bridges (DTF-C3). Devices based on these dyes exhibit a dramatically improved performance with the increasing π-bridge length, culminating with DTF-C3 in η = 8.29% under standard global AM 1.5 illumination.

  12. Dissolved organic matter removal using magnetic anion exchange resin treatment on biological effluent of textile dyeing wastewater.

    PubMed

    Fan, Jun; Li, Haibo; Shuang, Chendong; Li, Wentao; Li, Aimin

    2014-08-01

    This study investigated the removal of dissolved organic matter (DOM) from real dyeing bio-treatment effluents (DBEs) with the use of a novel magnetic anion exchange resin (NDMP). DOMs in two typical DBEs were fractionized using DAX-8/XAD-4 resin and ultrafiltration membranes. The hydrophilic fractions and the low molecular weight (MW) (<3kDa) DOM fractions constituted a major portion (>50%) of DOMs for the two effluents. The hydrophilic and low MW fractions of both effluents were the greatest contributors of specific UV254 absorbance (SUVA254), and the SUVA254 of DOM fractions decreased with hydrophobicity and MW. Two DBEs exhibited acute and chronic biotoxicities. Both acute and chronic toxicities of DOM fractions increased linearly with the increase of SUVA254 value. Kinetics of dissolved organic carbon (DOC) removal via NDMP treatment was performed by comparing it with that of particle active carbon (PAC). Results indicated that the removal of DOC from DBEs via NDMP was 60%, whereas DOC removals by PAC were lower than 15%. Acidic organics could be significantly removed with the use of NDMP. DOM with large MW in DBE could be removed significantly by using the same means. Removal efficiency of NDMP for DOM decreased with the decrease of MW. Compared with PAC, NDMP could significantly reduce the acute and chronic bio-toxicities of DBEs. NaCl/NaOH mixture regenerants, with selected concentrations of 10% NaCl (m/m)/1% NaOH (m/m), could improve desorption efficiency. PMID:25108712

  13. Highly efficient photocatalytic degradation of organic dyes by Cu doped ZnO nanostructures.

    PubMed

    Kuriakose, Sini; Satpati, Biswarup; Mohapatra, Satyabrata

    2015-10-14

    Copper doped ZnO nanostructures have been synthesized by a facile wet chemical method. Structural properties of as-synthesized nanomaterials have been studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy, while UV-visible absorption spectroscopy and Raman spectroscopy have been used to study their optical properties. Sunlight driven photocatalytic degradation of methylene blue (MB) and methyl orange (MO) dyes in water was used to evaluate the photocatalytic activities of Cu doped ZnO nanostructures using UV-visible absorption spectroscopy. The results showed that there is an optimum Cu doping level which leads to the highly enhanced photocatalytic activity of Cu doped ZnO nanostructures, as compared to pure ZnO nanostructures. A mechanism for the enhanced photocatalytic activity of Cu-ZnO nanostructures is tentatively proposed. The enhanced photocatalytic activity of Cu-ZnO nanostructures is attributed to the combined effects of improved separation of photogenerated charge carriers due to optimal Cu doping in ZnO nanostructures and the formation of ZnO-CuO nanoheterojunctions.

  14. Impact of local compressive stress on the optical transitions of single organic dye molecules

    NASA Astrophysics Data System (ADS)

    Stöttinger, Sven; Hinze, Gerald; Diezemann, Gregor; Oesterling, Ingo; Müllen, Klaus; Basché, Thomas

    2014-03-01

    The ability to mechanically control the optical properties of individual molecules is a grand challenge in nanoscience and could enable the manipulation of chemical reactivity at the single-molecule level. In the past, light has been used to alter the emission wavelength of individual molecules or modulate the energy transfer quantum yield between them. Furthermore, tensile stress has been applied to study the force dependence of protein folding/unfolding and of the chemistry and photochemistry of single molecules, although in these mechanical experiments the strength of the weakest bond limits the amount of applicable force. Here, we show that compressive stress modifies the photophysical properties of individual dye molecules. We use an atomic force microscope tip to prod individual molecules adsorbed on a surface and follow the effect of the applied force on the electronic states of the molecule by fluorescence spectroscopy. Applying a localized compressive force on an isolated molecule induces a stress that is redistributed throughout the structure. Accordingly, we observe reversible spectral shifts and even shifts that persist after retracting the microscope tip, which we attribute to transitions to metastable states. Using quantum-mechanical calculations, we show that these photophysical changes can be associated with transitions among the different possible conformers of the adsorbed molecule.

  15. Metal-chelate dye-controlled organization of Cd32S14(SPh)40(4-) nanoclusters into three-dimensional molecular and covalent open architecture.

    PubMed

    Zheng, Nanfeng; Lu, Haiwei; Bu, Xianhui; Feng, Pingyun

    2006-04-12

    Chalcogenide II-VI nanoclusters are usually prepared as isolated clusters and have defied numerous efforts to join them into covalent open-framework architecture with conventional templating methods such as protonated amines or inorganic cations commonly used to direct the formation of porous frameworks. Herein, we report the first templated synthesis of II-VI covalent superlattices from large II-VI tetrahedral clusters (i.e., [Cd32S14(SPh)38]2-). Our method takes advantage of low charge density of metal-chelate dyes that is a unique match with three-dimensional II-VI semiconductor frameworks in charge density, surface hydrophilicity-hydrophobicity, and spatial organization. In addition, metal-chelate dyes also serve to tune the optical properties of resulting dye semiconductor composite materials.

  16. Optimization of lasing in an inverted-opal titania photonic crystal cavity as an organic solid-state dye-doped laser.

    PubMed

    Zhang, Dingke; Chen, Shijian; Jiang, Maohua; Ye, Lijuan

    2014-11-10

    Lasing performance of a dye-doped laser by encapsulating orange fluorescent dye 4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran (DCM) with different concentrations in a highly ordered three-dimensional (3D) inverted-opal titania (TiO2) photonic crystal (PC) microcavity was studied. The lasing threshold and laser quality were improved by optimizing the concentration of the laser dye DCM. When the concentration of DCM is optimized to 10-4  mol/l, the photoluminescence (PL) efficiency of DCM is sufficient to achieve lasing emission and meanwhile no fluorescence quantum quenching occurs. Therefore, the emission spectrum was greatly narrowed and the threshold was significantly improved, which reached 0.8  mJ pulse-1 cm-2. Our findings are promising results toward the realization of fabricating a highly efficient low-threshold organic laser.

  17. Dye-sensitized MIL-101 metal organic frameworks loaded with Ni/NiO{sub x} nanoparticles for efficient visible-light-driven hydrogen generation

    SciTech Connect

    Liu, Xin-Ling; Wang, Rong; Yuan, Yu-Peng E-mail: cxue@ntu.edu.sg; Zhang, Ming-Yi; Xue, Can E-mail: cxue@ntu.edu.sg

    2015-10-01

    The Ni/NiO{sub x} particles were in situ photodeposited on MIL-101 metal organic frameworks as catalysts for boosting H{sub 2} generation from Erythrosin B dye sensitization under visible-light irradiation. The highest H{sub 2} production rate of 125 μmol h{sup −1} was achieved from the system containing 5 wt. % Ni-loaded MIL-101 (20 mg) and 30 mg Erythrosin B dye. Moreover, the Ni/NiO{sub x} catalysts show excellent stability for long-term photocatalytic reaction. The enhancement on H{sub 2} generation is attributed to the efficient charge transfer from photoexcited dye to the Ni catalyst via MIL-101. Our results demonstrate that the economical Ni/NiO{sub x} particles are durable and active catalysts for photocatalytic H{sub 2} generation.

  18. Optimization of lasing in an inverted-opal titania photonic crystal cavity as an organic solid-state dye-doped laser.

    PubMed

    Zhang, Dingke; Chen, Shijian; Jiang, Maohua; Ye, Lijuan

    2014-11-10

    Lasing performance of a dye-doped laser by encapsulating orange fluorescent dye 4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran (DCM) with different concentrations in a highly ordered three-dimensional (3D) inverted-opal titania (TiO2) photonic crystal (PC) microcavity was studied. The lasing threshold and laser quality were improved by optimizing the concentration of the laser dye DCM. When the concentration of DCM is optimized to 10-4  mol/l, the photoluminescence (PL) efficiency of DCM is sufficient to achieve lasing emission and meanwhile no fluorescence quantum quenching occurs. Therefore, the emission spectrum was greatly narrowed and the threshold was significantly improved, which reached 0.8  mJ pulse-1 cm-2. Our findings are promising results toward the realization of fabricating a highly efficient low-threshold organic laser. PMID:25402981

  19. High catalytic activity of magnetic CuFe2O4/graphene oxide composite for the degradation of organic dyes under visible light irradiation

    NASA Astrophysics Data System (ADS)

    Chen, Peng; Xing, Xiang; Xie, Huifang; Sheng, Qi; Qu, Hongxia

    2016-09-01

    Magnetic CuFe2O4/graphene oxide composite (CuFe2O4/GO) has been synthesized by hydrothermal method and showed excellent visible-light-photocatalytic activity for the degradation of different dyes as Rhodamine B (RhB) and acid orange II (AO7) with no need of H2O2. The Structure and morphology were investigated by XRD, FTIR and TEM and the performance of the catalyst was systematically investigated under various experimental conditions as pH, the dosage of catalyst, dye initial concentration, etc. The dyes degradation on CuFe2O4/GO was also remained in a level in the presence of OH2- radical scavenger (2-propanol), while it decreased in the presence of O2- radical scavenger (benzoquinone) and h+ radical scavenger (ammonium oxalate), indicating that O2- and h+ radicals were responsible for the dye degradation. The magnetic CuFe2O4/GO composite shows potential applications in organic dye water treatment due to its magnetically recyclability and powerful visible-light-photocatalytic activity.

  20. Relationship between temperature-induced changes in internal microscopic structures of poly(N-isopropylacrylamide) microgels and organic dye uptake behavior.

    PubMed

    Kureha, Takuma; Sato, Takaaki; Suzuki, Daisuke

    2014-07-29

    Temperature-induced changes in the internal structures of poly(N-isopropylacrylamide) (pNIPAm) microgels were evaluated by small-angle X-ray scattering (SAXS), and the results were used to explain organic dye uptake by the microgels. The dye uptake experiments were conducted using two organic dyes: cationic rhodamine 6G (R6G) and anionic erythrosine. In the SAXS investigation, the internal structures of the microgels were characterized in terms of the correlation length, ξ, and the distance, d*, which originated from the local packing of the isopropyl groups of two neighboring chains. With increasing temperature up to the volume phase transition temperature (VPTT) of the microgels, the correlation length, ξ, was increased and the distance, d*, was decreased. At the same time, the amounts of the dyes taken up by the pNIPAm microgels were increased, despite a decrease in the volume of the microgels. The results indicated that the pNIPAm chains were closer to each other due to the hydrophobic association of isopropyl groups, which resulted in the growth of the hydrophobic domains. Thus, the hydrophobic interactions between the dyes and pNIPAm were probably accompanied by the domain formation. With a further increase of temperature above the VPTT, the correlation length, ξ, was decreased and then not defined because the Ornstein-Zernike type contribution disappeared, and the distance, d*, was not largely changed. At the same time, the uptake amounts of the dyes per unit volume of the microgels were also not largely changed, which behaved similar to the distance, d*. It was probably due to the fact that the internal structures of the microgels were not largely changed because the isopropyl groups were in contact with each other. The view was supported by the result of the uptake study of the nonthermoresponsive microgels which did not have the hydrophobic isopropyl groups. PMID:25003512

  1. Organic dopant added polyvinylidene fluoride based solid polymer electrolytes for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Senthil, R. A.; Theerthagiri, J.; Madhavan, J.

    2016-02-01

    The effect of phenothiazine (PTZ) as dopant on PVDF/KI/I2 electrolyte was studied for the fabrication of efficient dye-sensitized solar cell (DSSC). The different weight percentage (wt%) ratios (0, 20, 30, 40 and 50%) of PTZ doped PVDF/KI/I2 electrolyte films were prepared by solution casting method using DMF as a solvent. The following techniques such as Fourier transform infrared (FT-IR), differential scanning calorimetry (DSC), X-ray diffractometer (XRD) and AC-impedance analysis have been employed to characterize the prepared polymer electrolyte films. The FT-IR studies revealed the complex formation between PVDF/KI/I2 and PTZ. The crystalline and amorphous nature of polymer electrolytes were confirmed by DSC and XRD analysis respectively. The ionic conductivities of polymer electrolyte films were calculated from the AC-impedance analysis. The undoped PVDF/KI/I2 electrolyte exhibited the ionic conductivity of 4.68×10-6 S cm-1 and this value was increased to 7.43×10-5 S cm-1 when PTZ was added to PVDF/KI/I2 electrolyte. On comparison with different wt% ratios, the maximum ionic conductivity was observed for 20% PTZ-PVDF/KI/I2 electrolyte. A DSSC assembled with the optimized wt % of PTZ doped PVDF/KI/I2 electrolyte exhibited a power conversion efficiency of 2.92%, than the undoped PVDF/KI/I2 electrolyte (1.41%) at similar conditions. Hence, the 20% PTZ-PVDF/KI/I2 electrolyte was found to be optimal for DSSC applications.

  2. Organic sensitizers featuring a planar indeno[1,2-b]-thiophene for efficient dye-sensitized solar cells.

    PubMed

    Lim, Kimin; Ju, Myung Jong; Song, Juman; Choi, In Taek; Do, Kwangsuk; Choi, Hyeju; Song, Kihyung; Kim, Hwan Kyu; Ko, Jaejung

    2013-08-01

    An efficient organic sensitizer (JK-306) featuring a planar indeno[1,2-b]thiophene as the π-linker of a bridging unit for dye-sensitized solar cells (DSSCs) was synthesized. The sensitizer had a strong molar absorption coefficient and a red-shifted absorption band compared with JK-305, which resulted in a significant increase in the short-circuit photocurrent density. We incorporated a highly congested bulky amino group into the 2',4'-dihexyloxybiphenyl-4-yl moiety, an electron donor, to diminish the charge recombination and to prevent aggregation of the sensitizer. Under standard AM 1.5G solar conditions, JK-306-sensitized cells in the presence of co-adsorbents chenodeoxycholic acid (CDCA) and 4-[bis(9,9-dimethyl-9H-fluoren-2-yl)amino]benzoic acid (HC-A), which afforded an overall conversion efficiency of 8.37% and 8.52%, respectively. Upon changing the I(-) /I3 (-) electrolyte to the Co(II) /Co(III) redox couple, the cell gave rise to a significantly improved conversion efficiency of 10.02% with the multifunctional HC-A, which is one of the highest values reported for DSSCs with a cobalt-based electrolyte. Furthermore, the JK-306-based solar cell with a polymer gel electrolyte revealed a high conversion efficiency of 7.61%, which is one of the highest values for cells based on organic sensitizers.

  3. Enhancing dye-sensitized solar cell performances by molecular engineering: highly efficient π-extended organic sensitizers.

    PubMed

    Grisorio, Roberto; De Marco, Luisa; Agosta, Rita; Iacobellis, Rosabianca; Giannuzzi, Roberto; Manca, Michele; Mastrorilli, Piero; Gigli, Giuseppe; Suranna, Gian Paolo

    2014-09-01

    This study deals with the synthesis and characterization of two π-extended organic sensitizers (G1 and G2) for applications in dye-sensitized solar cells. The materials are designed with a D-A-π-A structure constituted by i) a triarylamine group as the donor part, ii) a dithienyl-benzothiadiazole chromophore followed by iii) a further ethynylene-thiophene (G1) or ethynylene-benzene (G2) π-spacer and iv) a cyano-acrylic moiety as acceptor and anchoring part. An unusual structural extension of the π-bridge characterizes these structures. The so-configured sensitizers exhibit a broad absorption profile, the origin of which is supported by density functional theory. The absence of hypsochromic shifts as a consequence of deprotonation as well as notable optical and electrochemical stabilities are also observed. Concerning the performances in devices, electrochemical impedance spectroscopy indicates that the structural modification of the π-spacer mainly increases the electron lifetime of G2 with respect to G1. In devices, this feature translates into a superior power conversion efficiency of G2, reaching 8.1%. These results are comparable to those recorded for N719 and are higher with respect to literature congeners, supporting further structural engineering of the π-bridge extension in the search for better performing π-extended organic sensitizers.

  4. Straightforward fabrication of stable white LEDs by embedding of inorganic UV-LEDs into bulk polymerized polymethyl-methacrylate doped with organic dyes

    NASA Astrophysics Data System (ADS)

    di Martino, Daniela; Beverina, Luca; Sassi, Mauro; Brovelli, Sergio; Tubino, Riccardo; Meinardi, Francesco

    2014-03-01

    Stable white-emitting down-converted LEDs are straightforwardly prepared by bulk polymerization of an organic dye doped polymethyl-methacrylate (PMMA) shell directly on top of a highly efficient commercial blue-emitting InGaN LED. Our optimized polymerization procedure allows for extending the form factor of achievable luminescence converter (LUCO) material beyond the conventional thin film form and to directly produce devices with light bulb design. The selected organic dyes, the blue-emitting Coumarin 30 and a red-emitting diketopyrrolopyrrole derivative, exhibit high compatibility with the free radical polymerization reaction of the PMMA matrix and ensure high stability of the final hybrid device. The control of both the thickness of the PMMA shell and the concentration of the dopant dyes allow for fine tuning of the emission color of the LUCO LED and to obtain white light with CIE chromatic coordinates x = 0.32 and y = 0.33, with rendering index as high as 80. This simple and versatile procedure is not dye-exclusive and is therefore extendable to other molecular systems for color-tunable efficient solid-state lighting sources.

  5. Theoretica Study of Asymmetric Double D-π-A Organic Sensitizers for Efficient Dye-Sensitized Solar Cells.

    PubMed

    Kwon, Dong Yuel; Lee, Gun Hyung; Kim, Young Sik

    2015-03-01

    Three novel dye sensitizers that were based on asymmetric double D-π-A chains with phenoxazine (POZ) and diphenylamine (DPA) as electron donors and cyanoacetic acid (CA) and 2-(1,1- dicyanomethylene) rhodanine (RD) as electron acceptors (DCPR, DRPC, DRPR) were designed, theoretically investigated, and compared with the reference dye based on asymmetric double D-π-A chains (DCPC). Using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) calculations, we gained insight into the factors responsible for the photovoltaic properties of the dye sensitizers. Due to the different HOMO levels of each donor and the different LUMO levels of each acceptor, the absorption spectrum of each dye showed different shapes. Among the dyes, DRPR showed a broader and more bathochromically shifted absorption band than the other dies. It also showed a higher molar extinction coefficient than that of the reference dye (DCPC). This work suggests optimizing the chain of electron donors and acceptors in dye sensitizers based on asymmetric double D-π-A chains would produce good photovoltaic properties for dye-sensitized solar cells (DSSCs).

  6. Transparent Organic Photodetector using a Near-Infrared Absorbing Cyanine Dye

    NASA Astrophysics Data System (ADS)

    Zhang, Hui; Jenatsch, Sandra; de Jonghe, Jelissa; Nüesch, Frank; Steim, Roland; Véron, Anna C.; Hany, Roland

    2015-03-01

    Organic photodetectors are interesting for low cost, large area optical sensing applications. Combining organic semiconductors with discrete absorption bands outside the visible wavelength range with transparent and conductive electrodes allows for the fabrication of visibly transparent photodetectors. Visibly transparent photodetectors can have far reaching impact in a number of areas including smart displays, window-integrated electronic circuits and sensors. Here, we demonstrate a near-infrared sensitive, visibly transparent organic photodetector with a very high average visible transmittance of 68.9%. The transmitted light of the photodetector under solar irradiation exhibits excellent transparency colour perception and rendering capabilities. At a wavelength of 850 nm and at -1 V bias, the photoconversion efficiency is 17% and the specific detectivity is 1012 Jones. Large area photodetectors with an area of 1.6 cm2 are demonstrated.

  7. Transparent organic photodetector using a near-infrared absorbing cyanine dye.

    PubMed

    Zhang, Hui; Jenatsch, Sandra; De Jonghe, Jelissa; Nüesch, Frank; Steim, Roland; Véron, Anna C; Hany, Roland

    2015-03-24

    Organic photodetectors are interesting for low cost, large area optical sensing applications. Combining organic semiconductors with discrete absorption bands outside the visible wavelength range with transparent and conductive electrodes allows for the fabrication of visibly transparent photodetectors. Visibly transparent photodetectors can have far reaching impact in a number of areas including smart displays, window-integrated electronic circuits and sensors. Here, we demonstrate a near-infrared sensitive, visibly transparent organic photodetector with a very high average visible transmittance of 68.9%. The transmitted light of the photodetector under solar irradiation exhibits excellent transparency colour perception and rendering capabilities. At a wavelength of 850 nm and at -1 V bias, the photoconversion efficiency is 17% and the specific detectivity is 10(12) Jones. Large area photodetectors with an area of 1.6 cm(2) are demonstrated.

  8. Detection of volatile organic compounds through a sensing film of TiO II doped with organic dyes deposited on an optical fiber

    NASA Astrophysics Data System (ADS)

    Muñoz A., S.; Ramos M., J.; Martínez H., C.; Castillo M., J.; Beltrán P., G.; Palomino M., R.

    2007-03-01

    The necessity of detection and recognition of different types of gases, such as volatile organic compounds, which are frequently found in food and beverage industries among others, requires the development of different types of sensors. In this work, an application of optical fiber for the detection of volatile organic compounds, particularly ethanol is presented. The sensor was constructed removing a portion of the cladding and depositing instead a sensing titanium dioxide (TiO II) film doped with an organic dye (rhodamine 6G) by the sol-gel method. The sensor response was measured in a Teflon chamber where the sample to be measured was injected. A He-Ne laser beam was coupled to the fiber and the variation in the output power was measured which indicates the gas presence. The difference between the output power with and without gas gives a measure of the concentration that exists in the chamber. The experimental results showed that for an ethanol concentration range from 0 to 10500 ppm, the response of the sensor was approximately linear with a correlation coefficient of 0.9924.

  9. Film Properties and Polycrystallization of Organic Dyes on ITOs with Surface Treatment for Organic Light-Emitting Diodes

    NASA Astrophysics Data System (ADS)

    Iwama, Yuki; Mori, Tatsuo; Mizutani, Teruyoshi

    ITO(Indium-Tin-Oxide) has been now widely used as the transparent anode for organic light-emitting devices(OLEDs). We used various methods of ITO surface treatment and examined the effects of them by measuring contact angle and calculating surface energy. We also prepared OLEDs with ITO treated by each method, and estimated their characteristics. The surface of ITO treated by UV-O3 or O2-plasma was more hydrophilic than that treated by only organic rinse or no treatment, and consequently the characteristic of the OLED was improved. We suppose these treatments affect the hole injection from ITO into organic layer, due to ionization potential or surface cleanness. We also investigated time degradation of NPD films on the ITO substrates. The films deposited with high deposition rate porycrystallized faster.

  10. Synthesis of a Near-Infrared Emitting Squaraine Dye in an Undergraduate Organic Laboratory

    ERIC Educational Resources Information Center

    Marks, Patrick; Levine, Mindy

    2012-01-01

    Squaraines are a class of organic fluorophores that possess unique photophysical properties, including strong near-infrared absorption and emission. The synthesis of many squaraines involves the condensation of an electron-rich aromatic ring with squaric acid. These reactions are generally refluxed overnight in a benzene-butanol solvent mixture.…

  11. Enhancement of the antiviral and interferon-inducing activities of poly r(A-U) by carminic acid.

    PubMed

    Jamison, J M; Flowers, D G; Jamison, E; Kitareewan, S; Krabill, K; Rosenthal, K S; Tsai, C

    1988-01-01

    Experiments have been designed to systematically examine the effects of carminic acid (CAR) on the antiviral/interferon-inducing activity of poly r(A-U), using the human foreskin fibroblast-vesicular stomatitis virus bioassay system. Modulation of the antiviral/interferon-inducing activity of poly r(A-U) by carminic acid was examined at fixed poly r(A-U) concentrations of 0.05 mM or 0.2 mM while varying the carminic acid concentrations to produce variable CAR/ribonucleotide ratios ranging from 1:16 to 2:1. Carminic acid and poly r(A-U) were tested individually at the concentrations employed in the CAR/poly r(A-U) combinations. Neither the carminic acid alone nor poly r(A-U) alone were effective antiviral agents/interferon inducers. The antiviral/interferon-inducing activity of poly r(A-U) was potentiated twelve-fold at CAR/ribonucleotide ratios in the region of 1/6 to 1/4. These results suggest a synergism between the poly r(A-U) and the carminic acid at the concentrations employed in this study. PMID:2451107

  12. Dye Painting!

    ERIC Educational Resources Information Center

    Johnston, Ann

    This resource provides practical instructions for applying color and design directly to fabric. Basic information about the dye painting process is given. The guide addresses the technical aspects of fabric dye and color use and offers suggestions for fabric manipulation and dye application in order to achieve various design effects. This…

  13. Nickel-supported carbon nitride photocatalyst combined with organic dye for visible-light-driven hydrogen evolution from water.

    PubMed

    Mori, Kohsuke; Itoh, Taiki; Kakudo, Hiroki; Iwamoto, Tomoyuki; Masui, Yoichi; Onaka, Makoto; Yamashita, Hiromi

    2015-10-01

    A noble-metal-free photocatalytic H2 production system consisting of a Ni-based catalyst, visible-light-responsive organic dye, and graphitic carbon nitride (g-C3N4) as a support has been developed. Characterization by means of XAFS revealed that the deposition of a trinuclear Ni precursor complex, Ni(NiL2)2Cl2 (L = β-mercaptoethylamine), on the g-C3N4 affords a monomeric Ni(ii) species involving β-mercaptoethylamine and aqua ligands in an octahedral coordination geometry. Such a Ni species acts as a hydrogen production site from an aqueous solution without an electron relay reagent by combining with thiazole orange (TO) as a photosensitizer. The emission of the attached TO at around 550 nm decreases with increasing loading amount of Ni catalyst, suggesting electron transfer from TO to the Ni catalyst via the g-C3N4 support. Leaching and agglomeration of the active Ni catalyst and TO are not observed during the photocatalytic reaction. Moreover, the use of highly porous carbon nitride (nanoporous carbon nitride; nanoC3N4) is proven to significantly enhance the photocatalytic activity because of the high surface area due to the unique porous structure as well as high absorption and emission properties of TO associated with nanoC3N4.

  14. Influence of synthetic and natural food dyes on activities of CYP2A6, UGT1A6, and UGT2B7.

    PubMed

    Kuno, Nayumi; Mizutani, Takaharu

    2005-08-27

    Synthetic or natural food dyes are typical xenobiotics, as are drugs and pollutants. After ingestion, part of these dyes may be absorbed and metabolized by phase I and II drug-metabolizing enzymes and excreted by transporters of phase III enzymes. However, there is little information regarding the metabolism of these dyes. It was investigated whether these dyes are substrates for CYP2A6 and UDP-glucuronosyltransferase (UGT). The in vitro inhibition of drug-metabolizing enzymes by these dyes was also examined. The synthetic food dyes studied were amaranth (food red no. 2), erythrosine B (food red no. 3), allura red (food red no. 40), new coccine (food red no. 102), acid red (food red no. 106), tartrazine (food Yellow no. 4), sunset yellow FCF (food yellow no. 5), brilliant blue FCF (food blue no. 1), and indigo carmine (food blue no. 2). The natural additive dyes studied were extracts from purple sweet potato, purple corn, cochineal, monascus, grape skin, elderberry, red beet, gardenia, and curthamus. Data confirmed that these dyes were not substrates for CYP2A6, UGT1A6, and UGT2B7. Only indigo carmine inhibited CYP2A6 in a noncompetitive manner, while erythrosine B inhibited UGT1A6 (glucuronidation of p-nitrophenol) and UGT2B7 (glucuronidation of androsterone). In the natural additive dyes just listed, only monascus inhibited UGT1A6 and UGT2B7.

  15. Characterization of a Highly Thermostable and Organic Solvent-Tolerant Copper-Containing Polyphenol Oxidase with Dye-Decolorizing Ability from Kurthia huakuii LAM0618T

    PubMed Central

    Guo, Xiang; Zhou, Shan; Wang, Yanwei; Song, Jinlong; Wang, Huimin; Kong, Delong; Zhu, Jie; Dong, Weiwei; He, Mingxiong; Hu, Guoquan; Ruan, Zhiyong

    2016-01-01

    Laccases are green biocatalysts that possess attractive advantages for the treatment of resistant environmental pollutants and dye effluents. A putative laccase-like gene, laclK, encoding a protein of 29.3 kDa and belonging to the Cu-oxidase_4 superfamily, was cloned and overexpressed in Escherichia coli. The purified recombinant protein LaclK (LaclK) was able to oxidize typical laccase substrates such as 2,6-dimethoxyphenol and l-dopamine. The characteristic adsorption maximums of typical laccases at 330 nm and 610 nm were not detected for LaclK. Cu2+ was essential for substrate oxidation, but the ratio of copper atoms/molecule of LaclK was determined to only be 1:1. Notably, the optimal temperature of LaclK was 85°C with 2,6-dimethoxyphenol as substrates, and the half-life approximately 3 days at 80°C. Furthermore, 10% (v/v) organic solvents (methanol, ethanol, isopropyl alcohol, butyl alcohol, Triton x-100 or dimethyl sulfoxide) could promote enzymatic activity. LaclK exhibited wide-spectrum decolorization ability towards triphenylmethane dyes, azo dyes and aromatic dyes, decolorizing 92% and 94% of Victoria Blue B (25 μM) and Ethyl Violet (25 μM), respectively, at a concentration of 60 U/L after 1 h of incubation at 60°C. Overall, we characterized a novel thermostable and organic solvent-tolerant copper-containing polyphenol oxidase possessing dye-decolorizing ability. These unusual properties make LaclK an alternative for industrial applications, particularly processes that require high-temperature conditions. PMID:27741324

  16. Modeling materials and processes in hybrid/organic photovoltaics: from dye-sensitized to perovskite solar cells.

    PubMed

    De Angelis, Filippo

    2014-11-18

    CONSPECTUS: Over the last 2 decades, researchers have invested enormous research effort into hybrid/organic photovoltaics, leading to the recent launch of the first commercial products that use this technology. Dye-sensitized solar cells (DSCs) have shown clear advantages over competing technologies. The top certified efficiency of DSCs exceeds 11%, and the laboratory-cell efficiency is greater than 13%. In 2012, the first reports of high efficiency solid-state DSCs based on organohalide lead perovskites completely revolutionized the field. These materials are used as light absorbers in DSCs and as light-harvesting materials and electron conductors in meso-superstructured and flat heterojunction solar cells and show certified efficiencies that exceed 17%. To effectively compete with conventional photovoltaics, emerging technologies such as DSCs need to achieve higher efficiency and stability, while maintaining low production costs. Many of the advances in the DSC field have relied on the computational design and screening of new materials, with researchers examining material characteristics that can improve device performance or stability. Suitable modeling strategies allow researchers to observe the otherwise inaccessible but crucial heterointerfaces that control the operation of DSCs, offering the opportunity to develop new and more efficient materials and optimize processes. In this Account, we present a unified view of recent computational modeling research examining DSCs, illustrating how the principles and simulation tools used for these systems can also be adapted to study the emerging field of perovskite solar cells. Researchers have widely applied first-principles modeling to the DSC field and, more recently, to perovskite-based solar cells. DFT/TDDFT methods provide the basic framework to describe most of the desired materials and interfacial properties, and Car-Parrinello molecular dynamics allow researchers the further ability to sample local minima and

  17. Understanding flocculation mechanism of graphene oxide for organic dyes from water: Experimental and molecular dynamics simulation

    NASA Astrophysics Data System (ADS)

    Liu, Jun; Li, Peng; Xiao, Hang; Zhang, Yayun; Shi, Xiaoyang; Lü, Xiaomeng; Chen, Xi

    2015-11-01

    Flocculation treatment processes play an important role in water and wastewater pretreatment. Here we investigate experimentally and theoretically the possibility of using graphene oxide (GO) as a flocculant to remove methylene blue (MB) from water. Experimental results show that GO can remove almost all MB from aqueous solutions at its optimal dosages and molecular dynamics simulations indicate that MB cations quickly congregate around GO in water. Furthermore, PIXEL energy contribution analysis reveals that most of the strong interactions between GO and MB are of a van der Waals (London dispersion) character. These results offer new insights for shedding light on the molecular mechanism of interaction between GO and organic pollutants.

  18. Three-photon absorption process in organic dyes enhanced by surface plasmon resonance

    NASA Astrophysics Data System (ADS)

    Cohanoschi, Ion

    2006-07-01

    Multi-photon absorption processes have received significant attention from the scientific community during the last decade, mainly because of their potential applications in optical limiting, data storage and biomedical fields. Perhaps, one of the most investigated processes studied so far has been two-photon absorption (2PA). These investigations have resulted in successful applications in all the fields mentioned above. However, 2PA present some limitations in the biomedical field when pumping at typical 2PA wavelengths. In order to overcome these limitations, three-photon absorption (3PA) process has been proposed. However, 3PA in organic molecules has a disadvantage, typical values of sigma3' are small (10-81 cm6s 2/photon2), therefore, 3PA excitation requires high irradiances to induce the promotion of electrons from the ground state to the final excited state. To overcome this obstacle, specific molecules that exhibit large 3PA cross-section must be designed. Thus far, there is a lack of systematic studies that correlate 3PA processes with the molecular structure of organic compounds. In order to fill the existent gap in 3PA molecular engineering, in this dissertation we have investigated the structure/property relationship for a new family of fluorene derivatives with very high three-photon absorption cross-sections. We demonstrated that the symmetric intramolecular charge transfer as well as the pi-electron conjugation length enhances the 3PA cross-section of fluorene derivatives. In addition, we showed that the withdrawing electron character of the attractor groups in a pull-pull geometry proved greater 3PA cross-section. After looking for alternative ways to enhance the effective sigma 3' of organic molecules, we investigated the enhancement of two- and three-photon absorption processes by means of Surface Plasmon. We demonstrated an enhancement of the effective two- and three-photon absorption cross-section of an organic compound of 480 and 30 folds

  19. Solution-processed organic photovoltaic cells based on a squaraine dye.

    PubMed

    Chen, Guo; Sasabe, Hisahiro; Wang, Zhongqiang; Wang, Xiaofeng; Hong, Ziruo; Kido, Junji; Yang, Yang

    2012-11-14

    In this work, 2,4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl] squaraine (SQ) was systematically studied as an electron donor in solution processed photovoltaic cells, showing power conversion efficiency of >4.0% under AM1.5G 1 sun illumination at room temperature. Low mobilities were found to limit charge transport in the bulk heterojunctions. Efficiency was thus improved to 5.1% at 80 °C mainly due to improvement of photocurrent extraction. We also demonstrated that the SQ compound synthesized via a simple method has high purity, and thus can be used in photovoltaic cells without further purification. Our results suggest the huge potential of SQ and its analogs in organic photovoltaic applications.

  20. Re-evaluation of all-plastic organic dye laser with DFB structure fabricated using photoresists

    PubMed Central

    Tsutsumi, Naoto; Nagi, Saori; Kinashi, Kenji; Sakai, Wataru

    2016-01-01

    Organic solid-state lasers (OSSLs) with distributed feedback structures can detect nanoscale materials and therefore offer an attractive sensing platform for biological and medical applications. Here we investigate the lasing characteristics, i.e., the threshold and slope efficiency, as a function of the grating depth in OSSL devices with distributed feedback (DFB) structure fabricated using photoresists. Two types of photoresists were used for the DFB structures: a negative photoresist, SU-8 2002, and a positive photoresist, ma-P 1275. The DFB structure was fabricated using a Lloyd-mirror configuration. The active layer was a rhodamine 6G-doped cellulose acetate waveguide. The threshold for the first order mode (m  = 1) was lower than that for the second and third order modes (m = 2, and 3). A low threshold of 27 μJ cm−2 pulse−1 (58 nJ) was obtained using SU-8 2002, with m = 1. The slope efficiency was evaluated as a function of grating depth for each mode and increased as the grating depth increased. PMID:27703217

  1. Re-evaluation of all-plastic organic dye laser with DFB structure fabricated using photoresists

    NASA Astrophysics Data System (ADS)

    Tsutsumi, Naoto; Nagi, Saori; Kinashi, Kenji; Sakai, Wataru

    2016-10-01

    Organic solid-state lasers (OSSLs) with distributed feedback structures can detect nanoscale materials and therefore offer an attractive sensing platform for biological and medical applications. Here we investigate the lasing characteristics, i.e., the threshold and slope efficiency, as a function of the grating depth in OSSL devices with distributed feedback (DFB) structure fabricated using photoresists. Two types of photoresists were used for the DFB structures: a negative photoresist, SU-8 2002, and a positive photoresist, ma-P 1275. The DFB structure was fabricated using a Lloyd-mirror configuration. The active layer was a rhodamine 6G-doped cellulose acetate waveguide. The threshold for the first order mode (m  = 1) was lower than that for the second and third order modes (m = 2, and 3). A low threshold of 27 μJ cm‑2 pulse‑1 (58 nJ) was obtained using SU-8 2002, with m = 1. The slope efficiency was evaluated as a function of grating depth for each mode and increased as the grating depth increased.

  2. Advanced treatment of textile dyeing secondary effluent using magnetic anion exchange resin and its effect on organic fouling in subsequent RO membrane.

    PubMed

    Yang, Cheng; Li, Li; Shi, Jialu; Long, Chao; Li, Aimin

    2015-03-01

    Strict regulations are forcing dyeing factory to upgrade existing waste treatment system. In this study, advanced treatment of dyeing secondary effluent by magnetic anion exchange resin (NDMP) was investigated and compared with ultrafiltration (UF); NDMP as a pre-treatment of reverse osmosis (RO) was also studied. NDMP resin (20 mL/L) gave higher removal of dissolved organic carbon (DOC) (83.9%) and colority (94.9%) than UF with a cut-off of 10 kDa (only 48.6% and 44.1%, respectively), showing that NDMP treatment was effective to meet the stringent discharge limit of DOC and colority. Besides, NDMP resin (20 mL/L) as a pretreatment of RO increased the permeate flux by 12.5% and reduced irreversible membrane fouling by 6.6%, but UF pretreatment did not mitigate RO membrane fouling. The results of excitation-emission matrix fluorescence spectra and resin fractions showed that NDMP had more efficient removal than UF for transphilic acid and hydrophilic fraction, such as protein-like organic matters and soluble microbial products, which contributed to a significant proportion of RO membrane fouling. In sum, NDMP resin treatment not only gave effective removal of DOC and colority of dyeing secondary effluent, but exhibited some improvement for RO membrane flux and irreversible fouling. PMID:25463217

  3. Advanced treatment of textile dyeing secondary effluent using magnetic anion exchange resin and its effect on organic fouling in subsequent RO membrane.

    PubMed

    Yang, Cheng; Li, Li; Shi, Jialu; Long, Chao; Li, Aimin

    2015-03-01

    Strict regulations are forcing dyeing factory to upgrade existing waste treatment system. In this study, advanced treatment of dyeing secondary effluent by magnetic anion exchange resin (NDMP) was investigated and compared with ultrafiltration (UF); NDMP as a pre-treatment of reverse osmosis (RO) was also studied. NDMP resin (20 mL/L) gave higher removal of dissolved organic carbon (DOC) (83.9%) and colority (94.9%) than UF with a cut-off of 10 kDa (only 48.6% and 44.1%, respectively), showing that NDMP treatment was effective to meet the stringent discharge limit of DOC and colority. Besides, NDMP resin (20 mL/L) as a pretreatment of RO increased the permeate flux by 12.5% and reduced irreversible membrane fouling by 6.6%, but UF pretreatment did not mitigate RO membrane fouling. The results of excitation-emission matrix fluorescence spectra and resin fractions showed that NDMP had more efficient removal than UF for transphilic acid and hydrophilic fraction, such as protein-like organic matters and soluble microbial products, which contributed to a significant proportion of RO membrane fouling. In sum, NDMP resin treatment not only gave effective removal of DOC and colority of dyeing secondary effluent, but exhibited some improvement for RO membrane flux and irreversible fouling.

  4. [Case of urticaria due to cochineal dye in red-colored diet].

    PubMed

    Kotobuki, Yorihisa; Azukizawa, Hiroaki; Nishida, Youko; Murota, Hiroyuki; Katayama, Ichiro; Yoshikawa, Kunihiko

    2007-12-01

    We herein describe a 33-year-old female who recurrently exhibited urticaria accompanied by vomiting, diarrhea and dyspnea after taking red-colored food. From her history, we suspected the cochineal dye, the commonly used natural red dye in red-colored food and beverage, to be the cause of her symptoms. Oral provocation test using cochineal dye-stained red-colored boiled-fish-paste induced urticaria and respiratory symptoms. Furthermore the prick tests and the scratch tests with cochineal dye and carminic acid, the major ingredient of cochineal dye, were also positive. These results indicate that type 1 allergy to cochineal dye caused urticaria in this patient. Thereafter, she avoided the foods containing a cochineal dye and showed a complete clinical remission. Recently, the number of literatures described about increased incidence of type 1 allergy to cochineal dye. As the usage of cochineal dye is increasing in the Japanese market, we should keep in mind that cochineal dye can be a cause of urticaria in daily practice. PMID:18195555

  5. Extractive spectrophotometric and fluorimetric determination of boron with 2,2,4-trimethyl-1,3-pentanediaol and carminic acid.

    PubMed

    Aznarez, J; Ferrer, A; Rabadan, J M; Marco, L

    1985-12-01

    Boric acid at mug ml or ng ml level can be extracted from 1-6M hydrochloric acid into 2,2,4-trimethyl-1,3-pentanediol solution in chloroform and thus separated from many ions which interfere in the usual spectrophotometric methods. The boron is determined directly in the organic phase without back-extraction into water, by adding a solution of carminic acid in a mixture of sulphuric and glacial acetic acids (1+2 v v ) and measuring the absorbance at 549 nm. The molar absorptivity is 2.58 x 10(4) l.mole(-1).cm(-1) and Beer's law is valid for the 0.05-0.4 mug ml boron range. In the fluorimetric method, 509 or 547 nm can be used as the excitation wavelength and 567 nm for emission measurement, giving a linear response in the 8-120 ng ml boron range. Both methods have been applied to determination of boron in plants and natural waters with good precision and accuracy. PMID:18963973

  6. Degradation of Dye Wastewater by ns-Pulse DBD Plasma

    NASA Astrophysics Data System (ADS)

    Gao, Jin; Gu, Pingdao; Yuan, Li; Zhong, Fangchuan

    2013-09-01

    Two plasma reactors have been developed and used to degrade dye wastewater agents. The configuration of one plasma reactor is a comb-like extendable unit module consisting of 5 electrodes covered with a quartz tube and the other one is an array reactor which is extended from the unit module. The decomposition of wastewater by ns pulse dielectric barrier discharge (DBD) plasma have been carried out by atomizing the dyeing solutions into the reactors. During experiments, the indigo carmine has been treated as the waste agent. The measurements of UV-VIS absorption spectroscopy and the chemical oxygen demand (COD) are carried out to demonstrate the decomposition effect on the wastewater. It shows that the decoloration rate of 99% and the COD degradation rate of 65% are achieved with 15 min treatment in the unit reactor. The effect of electrical parameters on degradation has been studied in detail. Results from the array reactor indicate that it has a better degradation effect than the unit one. It can not only totally remove the chromogenic bond of the indigo carmine solution, but also effectively degrade unsaturated bonds. The decoloration rate reaches 99% after 10 min treatment, the decomposition rate of the unsaturated bond reaches 83% after 60 min treatment, and the COD degradation rate is nearly 74%.

  7. A cascaded QSAR model for efficient prediction of overall power conversion efficiency of all-organic dye-sensitized solar cells.

    PubMed

    Li, Hongzhi; Zhong, Ziyan; Li, Lin; Gao, Rui; Cui, Jingxia; Gao, Ting; Hu, Li Hong; Lu, Yinghua; Su, Zhong-Min; Li, Hui

    2015-05-30

    A cascaded model is proposed to establish the quantitative structure-activity relationship (QSAR) between the overall power conversion efficiency (PCE) and quantum chemical molecular descriptors of all-organic dye sensitizers. The cascaded model is a two-level network in which the outputs of the first level (JSC, VOC, and FF) are the inputs of the second level, and the ultimate end-point is the overall PCE of dye-sensitized solar cells (DSSCs). The model combines quantum chemical methods and machine learning methods, further including quantum chemical calculations, data division, feature selection, regression, and validation steps. To improve the efficiency of the model and reduce the redundancy and noise of the molecular descriptors, six feature selection methods (multiple linear regression, genetic algorithms, mean impact value, forward selection, backward elimination, and +n-m algorithm) are used with the support vector machine. The best established cascaded model predicts the PCE values of DSSCs with a MAE of 0.57 (%), which is about 10% of the mean value PCE (5.62%). The validation parameters according to the OECD principles are R(2) (0.75), Q(2) (0.77), and Qcv2 (0.76), which demonstrate the great goodness-of-fit, predictivity, and robustness of the model. Additionally, the applicability domain of the cascaded QSAR model is defined for further application. This study demonstrates that the established cascaded model is able to effectively predict the PCE for organic dye sensitizers with very low cost and relatively high accuracy, providing a useful tool for the design of dye sensitizers with high PCE.

  8. Photocatalytic degradation of organic reactive dyes over MnTiO3/TiO2 heterojunction composites under UV-visible irradiation.

    PubMed

    Sivakumar, Santhanam; Selvaraj, Ayyasamy; Ramasamy, Anaipalayam Kandasamy

    2013-01-01

    In this study, the photocatalytic degradation of organic reactive dyes have been investigated using MnTiO3/TiO2 heterojunction composites in the presence of electron acceptors under UV-Visible light irradiation. This MnTiO3/TiO2 heterojunction composites were prepared by annealing different mass ratios of pyrophanite MnTiO3 (3-11 wt%) and TiO2 at 300°C. All the MnTiO3/TiO2 heterojunction composites were characterized by spectral techniques like X-ray diffraction (XRD), scanning electron microscope (SEM) and diffused reflectance UV-visible spectroscopic analysis (DRS). Among them, 9 wt% MnTiO3/TiO2 heterojunction composites exhibited higher photocatalytic activity for the degradation of Reactive Blue 4 (RB 4). The photocatalytic efficiency of 9 wt% MnTiO3/TiO2 heterojunction composites was further enhanced by the addition of substantial amount of electron acceptors like hydrogen peroxide (H2O2) and ammonium peroxydisulfate ([NH4]2S2O8). The presence of oxidants (electron acceptors) facilitates the fast degradation of dye solution even in higher concentration upto 200 mg/L. The photocatalytic activity of MnTiO3/TiO2 heterojunction composites was also studied for the degradation of other four different structured reactive dyes. The extent of mineralization of these organic reactive dyes during photocatalytic degradation was estimated from COD analysis. MnTiO3/TiO2 heterojunction composites was also found to have good photostability in the presence of oxidants.

  9. A simple method for determination of carmine in food samples based on cloud point extraction and spectrophotometric detection.

    PubMed

    Heydari, Rouhollah; Hosseini, Mohammad; Zarabi, Sanaz

    2015-01-01

    In this paper, a simple and cost effective method was developed for extraction and pre-concentration of carmine in food samples by using cloud point extraction (CPE) prior to its spectrophotometric determination. Carmine was extracted from aqueous solution using Triton X-100 as extracting solvent. The effects of main parameters such as solution pH, surfactant and salt concentrations, incubation time and temperature were investigated and optimized. Calibration graph was linear in the range of 0.04-5.0 μg mL(-1) of carmine in the initial solution with regression coefficient of 0.9995. The limit of detection (LOD) and limit of quantification were 0.012 and 0.04 μg mL(-1), respectively. Relative standard deviation (RSD) at low concentration level (0.05 μg mL(-1)) of carmine was 4.8% (n=7). Recovery values in different concentration levels were in the range of 93.7-105.8%. The obtained results demonstrate the proposed method can be applied satisfactory to determine the carmine in food samples.

  10. Catalytic ozonation of organic pollutants from bio-treated dyeing and finishing wastewater using recycled waste iron shavings as a catalyst: Removal and pathways.

    PubMed

    Wu, Jin; Ma, Luming; Chen, Yunlu; Cheng, Yunqin; Liu, Yan; Zha, Xiaosong

    2016-04-01

    Catalytic ozonation of organic pollutants from actual bio-treated dyeing and finishing wastewater (BDFW) with iron shavings was investigated. Catalytic ozonation effectively removed organic pollutants at initial pH values of 7.18-7.52, and the chemical oxygen demand (COD) level decreased from 142 to 70 mg·L(-1) with a discharge limitation of 80 mg·L(-1). A total of 100% and 42% of the proteins and polysaccharides, respectively, were removed with a decrease in their contribution to the soluble COD from 76% to 41%. Among the 218 organic species detected by liquid chromatography-mass spectrometry, 58, 77, 79 and 4 species were completely removed, partially removed, increased and newly generated, respectively. Species including textile auxiliaries and dye intermediates were detected by gas chromatography-mass spectrometry. The inhibitory effect decreased from 51% to 33%, suggesting a reduction in the acute toxicity. The enhanced effect was due to hydroxyl radical (OH) oxidation, co-precipitation and oxidation by other oxidants. The proteins were removed by OH oxidation (6%), by direct ozonation, co-precipitation and oxidation by other oxidants (94%). The corresponding values for polysaccharides were 21% and 21%, respectively. In addition, the iron shavings behaved well in successive runs. These results indicated that the process was favorable for engineering applications for removal of organic pollutants from BDFW.

  11. Photooxidation of different organic dyes (RB, MO, TB, and BG) using Fe(III)-doped TiO 2 nanophotocatalyst prepared by novel chemical method

    NASA Astrophysics Data System (ADS)

    Ghorai, Tanmay K.; Biswas, Soumya K.; Pramanik, Panchanan

    2008-09-01

    The nano-structured Fe(III)-doped TiO 2 photocatalysts with anatase phase have been developed for the oxidation of non-biodegradable different organic dyes like methyl orange (MO), rhodamine B (RB), thymol blue (TB) and bromocresol green (BG) using UV-Hg-lamp. The different compositions of Fe xTi 1- xO 2 ( x = 0.005, 0.01, 0.05, and 0.1) nanocatalysts synthesized by chemical method (CM), have been characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectra, specific surface area (BET), transmission electronic microscopy (TEM) analysis, XPS, ESR and zeta potential. From XRD analysis, the results indicate that all the compositions of Fe(III) doped in TiO 2 catalysts gives only anatase phase not rutile phase. For complete degradation of all the solutions of the dyes (MO, RB, TB, and BG), the composition with x = 0.005 is more photoactive compared all other compositions of Fe xTi 1- xO 2, and degussa P25. The decolorization rate of different dyes decreases as Fe(III) concentration in TiO 2 increases. The energy band gap of Fe(III)-doped TiO 2 is found to be 2.38 eV. The oxidation state of iron has been found to be 3+ from XPS and ESR show that Fe 3+ is in low spin state.

  12. TiO2 Immobilized on Manihot Carbon: Optimal Preparation and Evaluation of Its Activity in the Decomposition of Indigo Carmine

    PubMed Central

    Antonio-Cisneros, Cynthia M.; Dávila-Jiménez, Martín M.; Elizalde-González, María P.; García-Díaz, Esmeralda

    2015-01-01

    Applications of carbon-TiO2 materials have attracted attention in nanotechnology due to their synergic effects. We report the immobilization of TiO2 on carbon prepared from residues of the plant Manihot, commercial TiO2 and glycerol. The objective was to obtain a moderate loading of the anatase phase by preserving the carbonaceous external surface and micropores of the composite. Two preparation methods were compared, including mixing dry precursors and immobilization using a glycerol slurry. The evaluation of the micropore blocking was performed using nitrogen adsorption isotherms. The results indicated that it was possible to use Manihot residues and glycerol to prepare an anatase-containing material with a basic surface and a significant SBET value. The activities of the prepared materials were tested in a decomposition assay of indigo carmine. The TiO2/carbon eliminated nearly 100% of the dye under UV irradiation using the optimal conditions found by a Taguchi L4 orthogonal array considering the specific surface, temperature and initial concentration. The reaction was monitored by UV-Vis spectrophotometry and LC-ESI-(Qq)-TOF-MS, enabling the identification of some intermediates. No isatin-5-sulfonic acid was detected after a 60 min photocatalytic reaction, and three sulfonated aromatic amines, including 4-amino-3-hydroxybenzenesulfonic acid, 2-(2-amino-5-sulfophenyl)-2-oxoacetic acid and 2-amino-5-sulfobenzoic acid, were present in the reaction mixture. PMID:25588214

  13. TiO2 immobilized on Manihot carbon: optimal preparation and evaluation of its activity in the decomposition of indigo carmine.

    PubMed

    Antonio-Cisneros, Cynthia M; Dávila-Jiménez, Martín M; Elizalde-González, María P; García-Díaz, Esmeralda

    2015-01-12

    Applications of carbon-TiO2 materials have attracted attention in nanotechnology due to their synergic effects. We report the immobilization of TiO2 on carbon prepared from residues of the plant Manihot, commercial TiO2 and glycerol. The objective was to obtain a moderate loading of the anatase phase by preserving the carbonaceous external surface and micropores of the composite. Two preparation methods were compared, including mixing dry precursors and immobilization using a glycerol slurry. The evaluation of the micropore blocking was performed using nitrogen adsorption isotherms. The results indicated that it was possible to use Manihot residues and glycerol to prepare an anatase-containing material with a basic surface and a significant SBET value. The activities of the prepared materials were tested in a decomposition assay of indigo carmine. The TiO2/carbon eliminated nearly 100% of the dye under UV irradiation using the optimal conditions found by a Taguchi L4 orthogonal array considering the specific surface, temperature and initial concentration. The reaction was monitored by UV-Vis spectrophotometry and LC-ESI-(Qq)-TOF-MS, enabling the identification of some intermediates. No isatin-5-sulfonic acid was detected after a 60 min photocatalytic reaction, and three sulfonated aromatic amines, including 4-amino-3-hydroxybenzenesulfonic acid, 2-(2-amino-5-sulfophenyl)-2-oxoacetic acid and 2-amino-5-sulfobenzoic acid, were present in the reaction mixture.

  14. TiO2 immobilized on Manihot carbon: optimal preparation and evaluation of its activity in the decomposition of indigo carmine.

    PubMed

    Antonio-Cisneros, Cynthia M; Dávila-Jiménez, Martín M; Elizalde-González, María P; García-Díaz, Esmeralda

    2015-01-01

    Applications of carbon-TiO2 materials have attracted attention in nanotechnology due to their synergic effects. We report the immobilization of TiO2 on carbon prepared from residues of the plant Manihot, commercial TiO2 and glycerol. The objective was to obtain a moderate loading of the anatase phase by preserving the carbonaceous external surface and micropores of the composite. Two preparation methods were compared, including mixing dry precursors and immobilization using a glycerol slurry. The evaluation of the micropore blocking was performed using nitrogen adsorption isotherms. The results indicated that it was possible to use Manihot residues and glycerol to prepare an anatase-containing material with a basic surface and a significant SBET value. The activities of the prepared materials were tested in a decomposition assay of indigo carmine. The TiO2/carbon eliminated nearly 100% of the dye under UV irradiation using the optimal conditions found by a Taguchi L4 orthogonal array considering the specific surface, temperature and initial concentration. The reaction was monitored by UV-Vis spectrophotometry and LC-ESI-(Qq)-TOF-MS, enabling the identification of some intermediates. No isatin-5-sulfonic acid was detected after a 60 min photocatalytic reaction, and three sulfonated aromatic amines, including 4-amino-3-hydroxybenzenesulfonic acid, 2-(2-amino-5-sulfophenyl)-2-oxoacetic acid and 2-amino-5-sulfobenzoic acid, were present in the reaction mixture. PMID:25588214

  15. Fluorescent nanoparticles based on a microporous organic polymer network: fabrication and efficient energy transfer to surface-bound dyes.

    PubMed

    Patra, Abhijit; Koenen, Jan-Moritz; Scherf, Ullrich

    2011-09-14

    Well-defined nanoparticles composed of a tetraphenylmethane-based microporous polymer network with an average particle diameter of 30-60 nm were fabricated by a miniemulsion polymerization technique. Strong green emission was observed and efficient excitation energy transfer from nanoparticles to surface-bound dye molecules was explored. PMID:21805006

  16. Ultrasonically assisted hydrothermal synthesis of activated carbon-HKUST-1-MOF hybrid for efficient simultaneous ultrasound-assisted removal of ternary organic dyes and antibacterial investigation: Taguchi optimization.

    PubMed

    Azad, F Nasiri; Ghaedi, M; Dashtian, K; Hajati, S; Pezeshkpour, V

    2016-07-01

    Activated carbon (AC) composite with HKUST-1 metal organic framework (AC-HKUST-1 MOF) was prepared by ultrasonically assisted hydrothermal method and characterized by FTIR, SEM and XRD analysis and laterally was applied for the simultaneous ultrasound-assisted removal of crystal violet (CV), disulfine blue (DSB) and quinoline yellow (QY) dyes in their ternary solution. In addition, this material, was screened in vitro for their antibacterial actively against Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa (PAO1) bacteria. In dyes removal process, the effects of important variables such as initial concentration of dyes, adsorbent mass, pH and sonication time on adsorption process optimized by Taguchi approach. Optimum values of 4, 0.02 g, 4 min, 10 mg L(-1) were obtained for pH, AC-HKUST-1 MOF mass, sonication time and the concentration of each dye, respectively. At the optimized condition, the removal percentages of CV, DSB and QY were found to be 99.76%, 91.10%, and 90.75%, respectively, with desirability of 0.989. Kinetics of adsorption processes follow pseudo-second-order model. The Langmuir model as best method with high applicability for representation of experimental data, while maximum mono layer adsorption capacity for CV, DSB and QY on AC-HKUST-1 estimated to be 133.33, 129.87 and 65.37 mg g(-1) which significantly were higher than HKUST-1 as sole material with Qm to equate 59.45, 57.14 and 38.80 mg g(-1), respectively.

  17. Two novel POM-based inorganic-organic hybrid compounds: synthesis, structures, magnetic properties, photodegradation and selective absorption of organic dyes.

    PubMed

    Dui, Xue-Jing; Yang, Wen-Bin; Wu, Xiao-Yuan; Kuang, Xiaofei; Liao, Jian-Zhen; Yu, Rongmin; Lu, Can-Zhong

    2015-05-28

    The hydrothermal reactions of a mixture of (NH4)6Mo7O24·4H2O, Cu(Ac)2·H2O and 3-bpo ligands at different temperatures result in the isolation of two novel inorganic-organic hybrid materials containing different but related isopolymolybdate units, [Cu(3-bpo)(H2O)(Mo4O13)]·3H2O () and [Cu2(3-bpo)2(Mo6O20)] (). The {Mo4O13}n chains in and unprecedented [Mo6O20](4-) isopolyhexamolybdate anions in are linked by octahedral Cu(2+) ions into two-dimensional hybrid layers. Interestingly, 3-bpo ligands in both and are located on either side of these hybrid layers and serve as arched footbridges to link Cu(ii) ions in the layer via pyridyl N-donors, and at the same time connect these hybrid layers into 3D supramolecular frameworks via weak MoNoxadiazole bonds. Another important point for is that water clusters are filled in the 1D channels surrounded by isopolytetramolybdate units. In addition, dye adsorption and photocatalytic properties of and magnetic properties of have been investigated. The results indicated that complex is not only a good heterogeneous photocatalyst in the degradation of methyl orange (MO) and methylene blue (MB), but also has high absorption capacity of MB at room temperature and can selectively capture MB molecules from binary mixtures of MB/MO or MB/RhB. All MB molecules absorbed on can be completely released and photodegraded in the presence of adequate peroxide. The temperature dependence of magnetic susceptibility revealed that complex exhibits antiferromagnetic ordering at about 5 K, and a spin-flop transition was observed at about 5.8 T at 2 K, indicating metamagnetic-like behaviour from antiferromagnetic to ferromagnetic phases.

  18. Adsorption kinetics and isotherm of anionic dyes onto organo-bentonite from single and multisolute systems.

    PubMed

    Shen, Dazhong; Fan, Jianxin; Zhou, Weizhi; Gao, Baoyu; Yue, Qinyan; Kang, Qi

    2009-12-15

    The performances of polydiallydimethylammonium modified bentonite (PDADMA-bentonite) as an adsorbent to remove anionic dyes, namely Acid Scarlet GR (AS-GR), Acid Turquoise Blue 2G (ATB-2G) and Indigo Carmine (IC), were investigated in single, binary and ternary dye systems. In adsorption from single dye solutions with initial concentration of 100 micromol/L, the dosage of PDADMA-bentonite needed to remove 95% dye was 0.42, 0.68 and 0.75 g/L for AS-GR, ATB-2G and IC, respectively. The adsorption isotherms of the three dyes obeyed the Langmuir isotherm model with the equilibrium constants of 0.372, 0.629 and 4.31 L/micromol, the saturation adsorption amount of 176.3, 149.2 and 228.7 micromol/g for ATB-2G, IC and AS-GR, respectively. In adsorption from mixed dye solutions, the isotherm of each individual dye followed an expanded Langmuir isotherm model and the relationship between the total amount of dyes adsorbed and the total equilibrium dye concentration was interpreted well by Langmuir isotherm model. In the region of insufficient dosage of PDADMA-bentonite, the dye with a larger affinity was preferentially removed by adsorption. Desorption was observed in the kinetic curve of the dye with lower affinity on PDADMA-bentonite surface by the competitive adsorption. The kinetics in single dye solution and the total adsorption of dyes in binary and ternary dye systems nicely followed pseudo-second-order kinetic model.

  19. Photocatalytic degradation of indigo carmine by hydrothermally synthesized Bi₂MoO ₆ in presence of EDTA.

    PubMed

    Sánchez Trinidad, C; Martínez-de la Cruz, A; López Cuéllar, E

    2015-01-01

    Bi2MoO6 oxide was synthesized by hydrothermal reaction in the presence of EDTA under different experimental conditions (time of reaction and EDTA concentration) in order to obtain materials with specific textural properties. It was determined that the addition of EDTA influences the final physical properties of Bi2MoO6. The photocatalytic activity of Bi2MoO6 samples was evaluated in the degradation reaction of indigo carmine (IC) in aqueous solution under solar radiation type. The best results as photocatalyst were obtained with the sample hydrothermally synthesized at 150 ºC for 4h in presence of a 0.031 M EDTA solution. This sample was able to whiten a solution of IC in a 94% after 120 min of lamp irradiation with t 1/2 = 31 min. In general, the samples prepared with lower concentrations of EDTA were the best photocatalysts. A gradual decrease in the activity was observed in the samples prepared with the same EDTA concentration as was increased in the reaction time. Beyond differences in morphology and textural properties of the samples prepared, the presence of EDTA by-products on the samples and the decomposition degree of it were important factors in determining the activity of the photocatalysts. Analysis of total organic carbon (TOC) of samples irradiated for 100 h confirmed that Bi2MoO6 oxide is able to mineralize the complex organic molecule of IC to CO2 and H2O in 55 %.

  20. Analysis of the phosphorescent dye concentration dependence of triplet-triplet annihilation in organic host-guest systems

    NASA Astrophysics Data System (ADS)

    Zhang, L.; van Eersel, H.; Bobbert, P. A.; Coehoorn, R.

    2016-10-01

    Using a novel method for analyzing transient photoluminescence (PL) experiments, a microscopic description is obtained for the dye concentration dependence of triplet-triplet annihilation (TTA) in phosphorescent host-guest systems. It is demonstrated that the TTA-mechanism, which could be a single-step dominated process or a diffusion-mediated multi-step process, can be deduced for any given dye concentration from a recently proposed PL intensity analysis. A comparison with the results of kinetic Monte Carlo simulations provides the TTA-Förster radius and shows that the TTA enhancement due to triplet diffusion can be well described in a microscopic manner assuming Förster- or Dexter-type energy transfer.

  1. Enhancement of a solar photo-Fenton reaction with ferric-organic ligands for the treatment of acrylic-textile dyeing wastewater.

    PubMed

    Soares, Petrick A; Batalha, Mauro; Souza, Selene M A Guelli U; Boaventura, Rui A R; Vilar, Vítor J P

    2015-04-01

    Literature describes a kinetic mineralization profile for most of acrylic-textile dyeing wastewaters using a photo-Fenton reaction characterized by a slow degradation process and high reactants consumption. This work tries to elucidate that the slow decay on DOC concentration is associated with the formation of stable complexes between Fe(3+) and textile auxiliary products, limiting the photoreduction of Fe(3+). This work also evaluates the enhancement of a solar photo-Fenton reaction through the use of different ferric-organic ligands applied to the treatment of a simulated acrylic-textile dyeing wastewater, as a pre-oxidation step to enhance its biodegradability. The photo-Fenton reaction was negatively affected by two dyeing auxiliary products: i) Sera(®) Tard A-AS, a surfactant mainly composed of alkyl dimethyl benzyl ammonium chloride and ii) Sera(®) Sperse M-IW, a dispersing agent composed of polyglycol solvents. The catalytic activity of the organic ligands toward the ferrous-catalysed system followed this order: Fe(III)-Oxalate > Fe(III)-Citrate > Fe(III)-EDDS, and all were better than the traditional photo-Fenton reaction. Different design parameters such as iron concentration, pH, temperature, flow conditions, UV irradiance and H2O2 addition strategy and dose were evaluated. The ferrioxalate induced photo-Fenton process presented the best results, achieving 87% mineralization after 9.3 kJUV L(-1) and allowing to work until near neutral pH values. As expected, the biodegradability of the textile wastewater was significantly enhanced during the photo-Fenton treatment, achieving a value of 73%, consuming 32.4 mM of H2O2 and 5.7 kJUV L(-1).

  2. Microencapsulated jabuticaba (Myrciaria cauliflora) extract added to fresh sausage as natural dye with antioxidant and antimicrobial activity.

    PubMed

    Baldin, Juliana Cristina; Michelin, Euder Cesar; Polizer, Yana Jorge; Rodrigues, Isabela; de Godoy, Silvia Helena Seraphin; Fregonesi, Raul Pereira; Pires, Manoela Alves; Carvalho, Larissa Tátero; Fávaro-Trindade, Carmen Silvia; de Lima, César Gonçalves; Fernandes, Andrezza Maria; Trindade, Marco Antonio

    2016-08-01

    The aim was to evaluate the addition of microencapsulated jabuticaba extract (MJE) to fresh sausage as natural dye with antioxidant and antimicrobial activity. Fresh sausages without dye, with cochineal carmine and with addition of 2% and 4% MJE were evaluated for chemical, microbiological and sensory properties during 15days of refrigerated storage. TBARS values were lower (P<0.05) throughout the storage period in sausages with 2% and 4% MJE (below 0.1mg of malondialdehyde/kg sample) than in control and carmine treatments (from 0.3 to 0.6mg of malondialdehyde/kg sample). T2% and T4% also showed lower microbial counts on storage days 4 and 15 for APCs. The addition of 4% MJE negatively influenced (P<0.05) sensory color, texture and overall acceptance attributes. On the other hand, T2% presented similar (P>0.05) sensory acceptance to control and carmine treatments in most of the attributes evaluated except for a decrease in color. Thus, addition of 2% MJE to fresh sausage can be considered as a natural pigment ingredient.

  3. Microencapsulated jabuticaba (Myrciaria cauliflora) extract added to fresh sausage as natural dye with antioxidant and antimicrobial activity.

    PubMed

    Baldin, Juliana Cristina; Michelin, Euder Cesar; Polizer, Yana Jorge; Rodrigues, Isabela; de Godoy, Silvia Helena Seraphin; Fregonesi, Raul Pereira; Pires, Manoela Alves; Carvalho, Larissa Tátero; Fávaro-Trindade, Carmen Silvia; de Lima, César Gonçalves; Fernandes, Andrezza Maria; Trindade, Marco Antonio

    2016-08-01

    The aim was to evaluate the addition of microencapsulated jabuticaba extract (MJE) to fresh sausage as natural dye with antioxidant and antimicrobial activity. Fresh sausages without dye, with cochineal carmine and with addition of 2% and 4% MJE were evaluated for chemical, microbiological and sensory properties during 15days of refrigerated storage. TBARS values were lower (P<0.05) throughout the storage period in sausages with 2% and 4% MJE (below 0.1mg of malondialdehyde/kg sample) than in control and carmine treatments (from 0.3 to 0.6mg of malondialdehyde/kg sample). T2% and T4% also showed lower microbial counts on storage days 4 and 15 for APCs. The addition of 4% MJE negatively influenced (P<0.05) sensory color, texture and overall acceptance attributes. On the other hand, T2% presented similar (P>0.05) sensory acceptance to control and carmine treatments in most of the attributes evaluated except for a decrease in color. Thus, addition of 2% MJE to fresh sausage can be considered as a natural pigment ingredient. PMID:27016672

  4. Determination of boron in produced water using the carminic acid assay.

    PubMed

    Floquet, Cedric F A; Sieben, Vincent J; MacKay, Bruce A; Mostowfi, Farshid

    2016-04-01

    Using the carminic acid assay, we determined the concentration of boron in oilfield waters. We investigated the effect of high concentrations of salts and dissolved metals on the assay performance. The influence of temperature, development time, reagent concentration, and water volume was studied. Ten produced and flowback water samples of different origins were measured, and the method was successfully validated against ICP-MS measurements. In water-stressed regions, produced water is a potential source of fresh water for irrigation, industrial applications, or consumption. Therefore, boron concentration must be determined and controlled to match the envisaged waste water reuse. Fast, precise, and onsite measurements are needed to minimize errors introduced by sample transportation to laboratories. We found that the optimum conditions for our application were a 5:1 mixing volume ratio (reagent to sample), a 1 g L(-1) carminic acid concentration in 99.99% sulfuric acid, and a 30 min reaction time at ambient temperature (20 °C to 23 °C). Absorption values were best measured at 610 nm and 630 nm and baseline corrected at 865 nm. Under these conditions, the sensitivity of the assay to boron was maximized while its cross-sensitivity to dissolved titanium, iron, barium and zirconium was minimized, alleviating the need for masking agents and extraction methods. PMID:26838405

  5. Carminic acid modified anion exchanger for the removal and preconcentration of Mo(VI) from wastewater.

    PubMed

    El-Moselhy, Medhat Mohamed; Sengupta, Arup K; Smith, Ryan

    2011-01-15

    Removal and preconcentration of Mo(VI) from water and wastewater solutions was investigated using carminic acid modified anion exchanger (IRA743). Various factors influencing the adsorption of Mo(VI), e.g. pH, initial concentration, and coexisting oxyanions were studied. Adsorption reached equilibrium within <10 min and was independent of initial concentration of Mo(VI). Studies were performed at different pH values to find the pH at which maximum adsorption occurred and was determined to be at a pH between 4.0 and 6.0. The Langmuir adsorption capacity (q(max)) was found to be 13.5mg Mo(VI)/g of the adsorbent. The results showed that modification of IRA743 with carminic acid is suitable for the removal of Mo(VI), as molybdate, from water and wastewater samples. The concentration of Mo(VI) was determined spectrophotometrically using bromopyrogallol red as a complexation reagent. This allows the determination of Mo(VI) in the range 1.0-100.0 μg/mL. The obtained material was subjected to efficient regeneration. PMID:20943315

  6. Organic Fluorescent Dyes Supported on Activated Boron Nitride: A Promising Blue Light Excited Phosphors for High-Performance White Light-Emitting Diodes

    NASA Astrophysics Data System (ADS)

    Li, Jie; Lin, Jing; Huang, Yang; Xu, Xuewen; Liu, Zhenya; Xue, Yanming; Ding, Xiaoxia; Luo, Han; Jin, Peng; Zhang, Jun; Zou, Jin; Tang, Chengchun

    2015-02-01

    We report an effective and rare-earth free light conversion material synthesized via a facile fabrication route, in which organic fluorescent dyes, i.e. Rhodamine B (RhB) and fluorescein isothiocyanate (FITC) are embedded into activated boron nitride (αBN) to form a composite phosphor. The composite phosphor shows highly efficient Förster resonance energy transfer and greatly improved thermal stability, and can emit at broad visible wavelengths of 500-650 nm under the 466 nm blue-light excitation. By packaging of the composite phosphors and a blue light-emitting diode (LED) chip with transparent epoxy resin, white LED with excellent thermal conductivity, current stability and optical performance can be realized, i.e. a thermal conductivity of 0.36 W/mk, a Commission Internationale de 1'Eclairage color coordinates of (0.32, 0.34), and a luminous efficiency of 21.6 lm.W-1. Our research opens the door toward to the practical long-life organic fluorescent dyes-based white LEDs.

  7. Organic Fluorescent Dyes Supported on Activated Boron Nitride: A Promising Blue Light Excited Phosphors for High-Performance White Light-Emitting Diodes

    PubMed Central

    Li, Jie; Lin, Jing; Huang, Yang; Xu, Xuewen; Liu, Zhenya; Xue, Yanming; Ding, Xiaoxia; Luo, Han; Jin, Peng; Zhang, Jun; Zou, Jin; Tang, Chengchun

    2015-01-01

    We report an effective and rare-earth free light conversion material synthesized via a facile fabrication route, in which organic fluorescent dyes, i.e. Rhodamine B (RhB) and fluorescein isothiocyanate (FITC) are embedded into activated boron nitride (αBN) to form a composite phosphor. The composite phosphor shows highly efficient Förster resonance energy transfer and greatly improved thermal stability, and can emit at broad visible wavelengths of 500–650 nm under the 466 nm blue-light excitation. By packaging of the composite phosphors and a blue light-emitting diode (LED) chip with transparent epoxy resin, white LED with excellent thermal conductivity, current stability and optical performance can be realized, i.e. a thermal conductivity of 0.36 W/mk, a Commission Internationale de 1'Eclairage color coordinates of (0.32, 0.34), and a luminous efficiency of 21.6 lm·W−1. Our research opens the door toward to the practical long-life organic fluorescent dyes-based white LEDs. PMID:25682730

  8. Microchip electrophoresis with background electrolyte containing polyacrylic acid and high content organic solvent in cyclic olefin copolymer microchips for easily adsorbed dyes.

    PubMed

    Wei, Xuan; Sun, Ping; Yang, Shenghong; Zhao, Lei; Wu, Jing; Li, Fengyun; Pu, Qiaosheng

    2016-07-29

    Plastic microchips can significantly reduce the fabrication cost but the adsorption of some analytes limits their application. In this work, background electrolyte containing ionic polymer and high content of organic solvent was adopted to eliminate the analyte adsorption and achieve highly efficient separation in microchip electrophoresis. Two dyes, rhodamine 6G (Rh6G) and rhodamine B (RhB) were used as the model analytes. By using methanol as the organic solvent and polyacrylic acid (PAA) as a multifunctional additive, successful separation of the two dyes within 75μm id. microchannels was realized. The role of PAA is multiple, including viscosity regulator, selectivity modifier and active additive for counteracting analyte adsorption on the microchannel surface. The number of theoretical plate of 7.0×10(5)/m was attained within an effective separation distance of 2cm using background electrolyte consisting 80% methanol, 0.36% PAA and 30mmol/L phosphate at pH 5.0. Under optimized conditions, relative standard deviations of Rh6G and RhB detection (n=5) were no more than 1.5% for migration time and 2.0% for peak area, respectively. The limit of detection (S/N=3) was 0.1nmol/L for Rh6G. The proposed technique was applied in the determination of both Rh6G and RhB in chilli powder and lipstick samples with satisfactory recoveries of 81.3-103.7%. PMID:27371017

  9. Quantum dots-based double imaging combined with organic dye imaging to establish an automatic computerized method for cancer Ki67 measurement

    NASA Astrophysics Data System (ADS)

    Wang, Lin-Wei; Qu, Ai-Ping; Liu, Wen-Lou; Chen, Jia-Mei; Yuan, Jing-Ping; Wu, Han; Li, Yan; Liu, Juan

    2016-02-01

    As a widely used proliferative marker, Ki67 has important impacts on cancer prognosis, especially for breast cancer (BC). However, variations in analytical practice make it difficult for pathologists to manually measure Ki67 index. This study is to establish quantum dots (QDs)-based double imaging of nuclear Ki67 as red signal by QDs-655, cytoplasmic cytokeratin (CK) as yellow signal by QDs-585, and organic dye imaging of cell nucleus as blue signal by 4‧,6-diamidino-2-phenylindole (DAPI), and to develop a computer-aided automatic method for Ki67 index measurement. The newly developed automatic computerized Ki67 measurement could efficiently recognize and count Ki67-positive cancer cell nuclei with red signals and cancer cell nuclei with blue signals within cancer cell cytoplasmic with yellow signals. Comparisons of computerized Ki67 index, visual Ki67 index, and marked Ki67 index for 30 patients of 90 images with Ki67 ≤ 10% (low grade), 10% < Ki67 < 50% (moderate grade), and Ki67 ≥ 50% (high grade) showed computerized Ki67 counting is better than visual Ki67 counting, especially for Ki67 low and moderate grades. Based on QDs-based double imaging and organic dye imaging on BC tissues, this study successfully developed an automatic computerized Ki67 counting method to measure Ki67 index.

  10. Microchip electrophoresis with background electrolyte containing polyacrylic acid and high content organic solvent in cyclic olefin copolymer microchips for easily adsorbed dyes.

    PubMed

    Wei, Xuan; Sun, Ping; Yang, Shenghong; Zhao, Lei; Wu, Jing; Li, Fengyun; Pu, Qiaosheng

    2016-07-29

    Plastic microchips can significantly reduce the fabrication cost but the adsorption of some analytes limits their application. In this work, background electrolyte containing ionic polymer and high content of organic solvent was adopted to eliminate the analyte adsorption and achieve highly efficient separation in microchip electrophoresis. Two dyes, rhodamine 6G (Rh6G) and rhodamine B (RhB) were used as the model analytes. By using methanol as the organic solvent and polyacrylic acid (PAA) as a multifunctional additive, successful separation of the two dyes within 75μm id. microchannels was realized. The role of PAA is multiple, including viscosity regulator, selectivity modifier and active additive for counteracting analyte adsorption on the microchannel surface. The number of theoretical plate of 7.0×10(5)/m was attained within an effective separation distance of 2cm using background electrolyte consisting 80% methanol, 0.36% PAA and 30mmol/L phosphate at pH 5.0. Under optimized conditions, relative standard deviations of Rh6G and RhB detection (n=5) were no more than 1.5% for migration time and 2.0% for peak area, respectively. The limit of detection (S/N=3) was 0.1nmol/L for Rh6G. The proposed technique was applied in the determination of both Rh6G and RhB in chilli powder and lipstick samples with satisfactory recoveries of 81.3-103.7%.

  11. Green synthesis of AgI-reduced graphene oxide nanocomposites: Toward enhanced visible-light photocatalytic activity for organic dye removal

    NASA Astrophysics Data System (ADS)

    Reddy, D. Amaranatha; Lee, Seunghee; Choi, Jiha; Park, Seonhwa; Ma, Rory; Yang, Haesik; Kim, Tae Kyu

    2015-06-01

    Novel reduced graphene oxide (RGO) enwrapped AgI nanocomposites were successfully fabricated by a facile template-free ultrasound-assisted method at room temperature. The structural, morphological, and optical studies demonstrate that the obtained nanostructures have good crystallinity and that the graphene nanosheets are decorated densely with AgI nanostructures. The photocatalytic activity of the composite was evaluated by the degradation of an organic dye, Rhodamine B (RhB), under visible-light irradiation. The results indicate that AgI with incorporated graphene exhibited much higher photocatalytic activity than the pure AgI due to the improved separation efficiency of the photogenerated carriers and that it prolonged the lifetime of the electron-hole pairs due to the chemical bonding between AgI and graphene. AgI (0.4 mg mL-1 of graphene oxide) nanocomposites displayed the highest photocatalytic degradation efficiency and the corresponding catalytic efficiencies within 70 min were ∼96%. Moreover, with the assistance of H2O2 the photocatalytic ability of the as-obtained AgI-RGO nanocomposites was enhanced. The corresponding catalytic efficiencies within 30 min were ∼96.8% (for 1 mL H2O2) under the same irradiation conditions. The excellent visible-light photocatalytic efficiency and luminescence properties make the AgI-RGO nanocomposites promising candidates for the removal of organic dyes for water purification and enable their application in near-UV white LEDs.

  12. Nickel Nanoparticle-Decorated Porous Carbons for Highly Active Catalytic Reduction of Organic Dyes and Sensitive Detection of Hg(II) Ions.

    PubMed

    Veerakumar, Pitchaimani; Chen, Shen-Ming; Madhu, Rajesh; Veeramani, Vediyappan; Hung, Chin-Te; Liu, Shang-Bin

    2015-11-11

    High surface area carbon porous materials (CPMs) synthesized by the direct template method via self-assembly of polymerized phloroglucinol-formaldehyde resol around a triblock copolymer template were used as supports for nickel nanoparticles (Ni NPs). The Ni/CPM materials fabricated through a microwave-assisted heating procedure have been characterized by various analytical and spectroscopic techniques, such as X-ray diffraction, field emission transmission electron microscopy, vibrating sample magnetometry, gas physisorption/chemisorption, thermogravimetric analysis, and Raman, Fourier-transform infrared, and X-ray photon spectroscopies. Results obtained from ultraviolet-visible (UV-vis) spectroscopy demonstrated that the supported Ni/CPM catalysts exhibit superior activity for catalytic reduction of organic dyes, such as methylene blue (MB) and rhodamine B (RhB). Further electrochemical measurements by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) also revealed that the Ni/CPM-modified electrodes showed excellent sensitivity (59.6 μA μM(-1) cm(-2)) and a relatively low detection limit (2.1 nM) toward the detection of Hg(II) ion. The system has also been successfully applied for the detection of mercuric ion in real sea fish samples. The Ni/CPM nanocomposite represents a robust, user-friendly, and highly effective system with prospective practical applications for catalytic reduction of organic dyes as well as trace level detection of heavy metals. PMID:26479076

  13. Dye Painting with Fiber Reactive Dyes

    ERIC Educational Resources Information Center

    Benjamin-Murray, Betsy

    1977-01-01

    In her description of how to use dyes directly onto fabrics the author lists materials to be used, directions for mixing dyes, techniques for applying dyes, references for additional reading and sources for dye materials. Preceding the activity with several lessons in design and other textile techniques with the dye process will ensure a…

  14. 76 FR 3584 - Disclosure of Cochineal Extract and Carmine in the Labeling of Wines, Distilled Spirits, and Malt...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-20

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF THE TREASURY Alcohol and Tobacco Tax and Trade Bureau 27 CFR Parts 5 RIN 1513-AB79 Disclosure of Cochineal Extract and Carmine in the Labeling of Wines, Distilled Spirits, and Malt Beverages Correction In proposed...

  15. Multifunctional conjugated polymers with main-chain donors and side-chain acceptors for dye sensitized solar cells (DSSCs) and organic photovoltaic cells (OPVs).

    PubMed

    Chang, Dong Wook; Ko, Seo-Jin; Kim, Jin Young; Park, Su-Moon; Lee, Hyo Joong; Dai, Liming; Baek, Jong-Beom

    2011-11-15

    A novel multifunctional conjugated polymer (RCP-1) composed of an electron-donating backbone (carbazole) and an electron-accepting side chain (cyanoacetic acid) connected through conjugated vinylene and terthiophene has been synthesized and tested as a photosensitizer in two major molecule-based solar cells, namely dye sensitized solar cells (DSSCs) and organic photovoltaic cells (OPVs). Promising initial results on overall power conversion efficiencies of 4.11% and 1.04% are obtained from the basic structure of DSSCs and OPVs based on RCP-1, respectively. The well-defined donor (D)-acceptor (A) structure of RCP-1 has made it possible, for the first time, to reach over 4% of power conversion efficiency in DSSCs with an organic polymer sensitizer and good operation stability.

  16. Study of nonlinear refraction of organic dye by Z-scan technique using He-Ne laser

    SciTech Connect

    Medhekar, S.; Kumar, R.; Mukherjee, S.; Choubey, R. K.

    2013-02-05

    Laser induced third-order nonlinear optical responses of Brilliant Green solution has been investigated by utilizing single beam Z-scan technique with a continuous-wave He-Ne laser radiation at 632.8 nm. It was observed that the material exhibits self-defocusing type optical nonlinearity. The measurements of nonlinear refraction were carried out at different dye concentrations and found that the increase in solution concentration leads to the linear increase of the nonlinear refractive index. The experimental results confirm great potential of the Brilliant Green for the application in nonlinear optical devices.

  17. Graphene nanoplatelets doped with N at its edges as metal-free cathodes for organic dye-sensitized solar cells.

    PubMed

    Ju, Myung Jong; Jeon, In-Yup; Kim, Jae Cheon; Lim, Kimin; Choi, Hyun-Jung; Jung, Sun-Min; Choi, In Taek; Eom, Yu Kyung; Kwon, Young Jin; Ko, Jaejung; Lee, Jae-Joon; Kim, Hwan Kyu; Baek, Jong-Beom

    2014-05-21

    Challenging precious Pt-based electrocatalysts for dye-sensitized solar cells (DSSCs), graphene nanoplatelets that are N-doped at the edges (NGnPs) are prepared via simply ball-milling graphite in the presence of nitrogen gas. DSSCs based on specific nanoplatelets designated "NGnP5" display superior photovoltaic performance (power conversion efficiency, 10.27%) compared to that of conventional Pt-based devices (9.96%). More importantly, the NGnP counter electrode exhibits outstanding electrochemical stability and electrocatalytic activity with a cobalt-complex redox couple.

  18. Treatment of a textile effluent from dyeing with cochineal extracts using Trametes versicolor fungus.

    PubMed

    Arroyo-Figueroa, Gabriela; Ruiz-Aguilar, Graciela M L; López-Martínez, Leticia; González-Sánchez, Guillermo; Cuevas-Rodríguez, Germán; Rodríguez-Vázquez, Refugio

    2011-01-01

    Trametes versicolor (Tv) fungus can degrade synthetic dyes that contain azo groups, anthraquinone, triphenylmethane polymers, and heterocyclic groups. However, no references have been found related to the degradation of natural dyes, such as the carminic acid that is contained in the cochineal extract. Experiments to determine the decolorization of the effluent used in the cotton dyeing process with cochineal extract by means of Tv fungus were done. Treatments to determine decolorization in the presence or absence of Kirk's medium, glucose, and fungus, with an addition of 50% (v v-1) of nonsterilized effluent were performed. Physicochemical characterization was performed at the start and end of the treatment. Degradation kinetics were determined. A direct relationship was found between the dry weight of fungi, pH, and the decolorization system, with higher decolorization at lower pH levels (pH ~4.3). High decolorization (81% ± 0.09; 88% ± 0.17; and 99% ± 0.04) for three of the eight treatments (Kirk's medium without glucose, Kirk's medium with glucose, and without medium with glucose, respectively) was found. Toxicity tests determined an increase in the initial effluent toxicity (7.33 TU) compared with the final treatment (47.73 TU) in a period of 11 days. For this system, a degradation sequence of the carminic acid structure present in the effluent by the Tv fungus is suggested, in which it is seen that metabolites still containing aromatic structures are generated. PMID:21552764

  19. [Study on removal effect of different organic fractions from bio-treated effluent of dye wastewater by UV/H2O2 process].

    PubMed

    Li, Xin; Liu, Yong-di; Sun, Xian-bo; Xu, Hong-yong; Qian, Fei-yue; Li, Xin-jue; Li, Mu

    2012-08-01

    The pretreatment of bio-treated effluent of dye wastewater by UV/H2O2 process was studied. The influencing factors, such as H2O2 dosage, reaction time and pH values were evaluated for the removal efficiency of UV254, ADMI7.6, DOC and DOC of dye wastewater by UV/H2O2 process. The experimental results showed that,the optimal conditions determined were as follows: initial pH 7.4-8.1, H2O2 dosage 4.5 mmol x L(-1) and UV irradiation time of 50 min. Under the optimal conditions, UV254, ADMI7.6, DOC and COD removal rate could reach 77%, 94%, 40% and 69%. Removal effects of four different DOM fractions, hydrophobic acids, non-acid hydrophobics, tasnsphilics and hydrophilics separated by XAD-8 and XAD-4 resins. The experimental results show that: hydrophobic material was the main substance causing color, when it was characterized by ADMI7.6, the proportion could reach 92%, of which 53% was non-acid hydrophobics. It indicated that removal efficiencies of tasnsphilics, hydrophobic acids and non-acid hydrophobics were high through UV/H2O2, process, while hydrophilics' efficiencies were lower. The experimental results showed that organic molecules with molecular weight over 10,000 contributed greatly to UV254, ADMI7.6 and DOC removal rate. PMID:23213897

  20. J-aggregates of organic dye molecules complexed with iron oxide nanoparticles for imaging-guided photothermal therapy under 915-nm light.

    PubMed

    Song, Xuejiao; Gong, Hua; Liu, Teng; Cheng, Liang; Wang, Chao; Sun, Xiaoqi; Liang, Chao; Liu, Zhuang

    2014-11-12

    Recently, the development of nano-theranostic agents aiming at imaging guided therapy has received great attention. In this work, a near-infrared (NIR) heptamethine indocyanine dye, IR825, in the presence of cationic polymer, polyallylamine hydrochloride (PAH), forms J-aggregates with red-shifted and significantly enhanced absorbance. After further complexing with ultra-small iron oxide nanoparticles (IONPs) and the followed functionalization with polyethylene glycol (PEG), the obtained IR825@PAH-IONP-PEG composite nanoparticles are highly stable in different physiological media. With a sharp absorbance peak, IR825@PAH-IONP-PEG can serve as an effective photothermal agent under laser irradiation at 915 nm, which appears to be optimal in photothermal therapy application considering its improved tissue penetration compared with 808-nm light and much lower water heating in comparison to 980-nm light. As revealed by magnetic resonance (MR) imaging, those nanoparticles after intravenous injection exhibit high tumor accumulation, which is then harnessed for in vivo photothermal ablation of tumors, achieving excellent therapeutic efficacy in a mouse tumor model. This study demonstrates for the first time that J-aggregates of organic dye molecules are an interesting class of photothermal material, which when combined with other imageable nanoprobes could serve as a theranostic agent for imaging-guided photothermal therapy of cancer.

  1. Evaluation of the treatment performance of lab-scaled vertical flow constructed wetlands in removal of organic compounds, color and nutrients in azo dye-containing wastewater.

    PubMed

    Dogdu, Gamze; Yalcuk, Arda

    2016-01-01

    The objective of this study is to examine the treatment performance of vertical flow intermittent feeding constructed wetland (VFCW) in removal of organic pollution, nutrients and color in azo-dye containing wastewater. The systems consisted of PVC reactors, some filling materials such as gravel, sand and zeolite and wetland plants including Typha angustifolia and Canna indica. The average treatment efficiency of the systems for COD, color, sulphate, NH4-N, and PO4-P were in the range of 57-63%, 94-99%, 44-48%, 39-44%, and 84-88%, respectively among the VFCW reactors. It is concluded that VFCW reactor system can effectively be used in the treatment of dye-rich wastewater, especially for the removal of color and in the reduction of COD. Biofilm formation and cleavage of azo bonds could be observed by SEM and FTIR results, respectively. Almost similar NH4-N and PO4-P removal were obtained in all reactors by using same amount of zeolite media.

  2. Vertical-cavity surface-emitting laser in the long-wavelength (700 nm) region in the visible by energy transfer between organic dyes

    NASA Astrophysics Data System (ADS)

    Liao, Zhifu; Zhou, Yuan; Cui, Yuanjing; Yang, Yu; Wang, Zhiyu; Qian, Guodong

    2014-06-01

    In this work, organic vertical-cavity surface-emitting lasers (VCSELs) with single-mode laser output in the long-wavelength region (~700 nm) of the visible were reported based on the energy transfer between dye pairs consisting of pyrromethene 597 (PM597) and rhodamine 700 (LD700). By co-doping PM597 into the polymeric hosts, the fluorescence intensity of LD700 was enhanced by 30-fold and the photophysical parameters of the donor-acceptor pairs were investigated, indicating the involvement of non-radiative resonance energy transfer processes between PM597 and LD700. Active distributed Bragg reflectors (DBR) were made by alternately spin-coating dye-doped polyvinylcarbazole and cellulose acetate thin films as the high and low refractive index layers, respectively. By sandwiching the active layer with 2 DBR mirrors, VCSEL emission at 698.9 nm in the biological first window (650-950 nm) was observed under the 532-nm laser pulses. The laser slope efficiency and threshold were also measured.

  3. [Study on removal effect of different organic fractions from bio-treated effluent of dye wastewater by UV/H2O2 process].

    PubMed

    Li, Xin; Liu, Yong-di; Sun, Xian-bo; Xu, Hong-yong; Qian, Fei-yue; Li, Xin-jue; Li, Mu

    2012-08-01

    The pretreatment of bio-treated effluent of dye wastewater by UV/H2O2 process was studied. The influencing factors, such as H2O2 dosage, reaction time and pH values were evaluated for the removal efficiency of UV254, ADMI7.6, DOC and DOC of dye wastewater by UV/H2O2 process. The experimental results showed that,the optimal conditions determined were as follows: initial pH 7.4-8.1, H2O2 dosage 4.5 mmol x L(-1) and UV irradiation time of 50 min. Under the optimal conditions, UV254, ADMI7.6, DOC and COD removal rate could reach 77%, 94%, 40% and 69%. Removal effects of four different DOM fractions, hydrophobic acids, non-acid hydrophobics, tasnsphilics and hydrophilics separated by XAD-8 and XAD-4 resins. The experimental results show that: hydrophobic material was the main substance causing color, when it was characterized by ADMI7.6, the proportion could reach 92%, of which 53% was non-acid hydrophobics. It indicated that removal efficiencies of tasnsphilics, hydrophobic acids and non-acid hydrophobics were high through UV/H2O2, process, while hydrophilics' efficiencies were lower. The experimental results showed that organic molecules with molecular weight over 10,000 contributed greatly to UV254, ADMI7.6 and DOC removal rate.

  4. New composites of nanoparticle Cu (I) oxide and titania in a novel inorganic polymer (geopolymer) matrix for destruction of dyes and hazardous organic pollutants.

    PubMed

    Falah, Mahroo; MacKenzie, Kenneth J D; Knibbe, Ruth; Page, Samuel J; Hanna, John V

    2016-11-15

    New photoactive composites to efficiently remove organic dyes from water are reported. These consist of Cu2O/TiO2 nanoparticles in a novel inorganic geopolymer matrix modified by a large tertiary ammonium species (cetyltrimethylammonium bromide, CTAB) whose presence in the matrix is demonstrated by FTIR spectroscopy. The CTAB does not disrupt the tetrahedral geopolymer structural silica and alumina units as demonstrated by (29)Si and (27)Al MAS NMR spectroscopy. SEM/EDS, TEM and BET measurements suggest that the Cu2O/TiO2 nanoparticles are homogenously distributed on the surface and within the geopolymer pores. The mechanism of removal of methylene blue (MB) dye from solution consists of a combination of adsorption (under dark conditions) and photodegradation (under UV radiation). MB adsorption in the dark follows pseudo second-order kinetics and is described by Freundlich-Langmuir type isotherms. The performance of the CTAB-modified geopolymer based composites is superior to composites based on unmodified geopolymer hosts, the most effective composite containing 5wt% Cu2O/TiO2 in a CTAB-modified geopolymer host. These composites constitute a new class of materials with excellent potential in environmental protection applications.

  5. Organic-free Anatase TiO₂ Paste for Efficient Plastic Dye-Sensitized Solar Cells and Low Temperature Processed Perovskite Solar Cells.

    PubMed

    Fu, Nianqing; Huang, Chun; Liu, Yan; Li, Xing; Lu, Wei; Zhou, Limin; Peng, Feng; Liu, Yanchun; Huang, Haitao

    2015-09-01

    Recently, the synthesis of fine TiO2 paste with organic-free binder emerged as an indispensable technique for plastic photovoltaics due to the low temperature processing requirement. In this study, pure anatase TiO2 nanoparticles and organic-free TiO2-sol were successfully synthesized individually in organic-free solution. By mixing the pure anatase TiO2 with the newly developed TiO2-sol binder, mechanically robust and well-interconnected TiO2 films were prepared via UV-irradiation at low temperature for applications in plastic dye-sensitized solar cells (p-DSSCs). The structural, electrical, and photovoltaic properties of the films as well as the devices were investigated by various techniques. The dye-loading amount of the obtained film is 2.6 times that of the P25 electrodes. As revealed by electrochemical impedance spectroscopy results, the film derived from the as-prepared anatase TiO2 paste (A-TiO2) exhibits much smaller charge transport resistance and lower electron recombination rate than the P25 film, while the introduction of TiO2-sol into the paste can further remarkably decrease the resistance of the produced film (AS-TiO2). The p-DSSCs employing AS-TiO2 photoanode yield a high efficiency up to 7.51%, which is 86% higher than the P25 reference cells and also 31% higher than the A-TiO2 cell. As a proof of concept, the newly developed AS-TiO2 paste was also applied to low temperature processed perovskite solar cells (PSCs), and a promising high efficiency up to 9.95% was achieved.

  6. A hydrazone covalent organic polymer based micro-solid phase extraction for online analysis of trace Sudan dyes in food samples.

    PubMed

    Zhang, Chengjiang; Li, Gongke; Zhang, Zhuomin

    2015-11-01

    Covalent organic polymers (COPs) connected by covalent bonds are a new class of porous network materials with large surface area and potential superiority in sample pretreatment. In this study, a new hydrazone linked covalent organic polymer (HL-COP) adsorbent was well-designed and synthesized based on a simple Schiff-base reaction. The condensation of 1,4-phthalaldehyde and 1,3,5-benzenetricarbohydrazide as organic building blocks led to the synthesis of HL-COP with uniform particle size and good adsorption performance. This HL-COP adsorbent with high hydrophobic property and rich stacking π electrons contained abundant phenyl rings and imine (CN) groups throughout the entire molecular framework. The adsorption mechanism was explored and discussed based on π-π affinity, hydrophobic effect, hydrogen bonding and electron-donor-acceptor (EDA) interaction, which contributed to its strong recognition affinity to target compounds. Enrichment factors were 305-757 for six Sudan dyes by HL-COP micro-solid phase extraction (μ-SPE), indicating its remarkable preconcentration ability. Furthermore, the adsorption amounts by HL-COP μ-SPE were 1.0-11.0 folds as those by three commonly used commercial adsorbents. Then, HL-COP was applied as adsorbent of online μ-SPE coupled with high performance liquid chromatography (HPLC) for enrichment and analysis of trace Sudan dyes in food samples with detection limit of 0.03-0.15μg/L. The method was successfully applied for online analysis of chilli powder and sausage samples. Sudan II and Sudan III in one positive chilli powder sample were actually found and determined with concentrations of 8.3 and 6.8μg/kg, respectively. The recoveries of chilli powder and sausage samples were in range of 75.8-108.2% and 73.8-112.6% with relative standard deviations of 1.2-8.5% and 1.9-9.4% (n=5), respectively. The proposed method was accurate, reliable and convenient for the online simultaneous analysis of trace Sudan dyes in food samples. PMID

  7. A hydrazone covalent organic polymer based micro-solid phase extraction for online analysis of trace Sudan dyes in food samples.

    PubMed

    Zhang, Chengjiang; Li, Gongke; Zhang, Zhuomin

    2015-11-01

    Covalent organic polymers (COPs) connected by covalent bonds are a new class of porous network materials with large surface area and potential superiority in sample pretreatment. In this study, a new hydrazone linked covalent organic polymer (HL-COP) adsorbent was well-designed and synthesized based on a simple Schiff-base reaction. The condensation of 1,4-phthalaldehyde and 1,3,5-benzenetricarbohydrazide as organic building blocks led to the synthesis of HL-COP with uniform particle size and good adsorption performance. This HL-COP adsorbent with high hydrophobic property and rich stacking π electrons contained abundant phenyl rings and imine (CN) groups throughout the entire molecular framework. The adsorption mechanism was explored and discussed based on π-π affinity, hydrophobic effect, hydrogen bonding and electron-donor-acceptor (EDA) interaction, which contributed to its strong recognition affinity to target compounds. Enrichment factors were 305-757 for six Sudan dyes by HL-COP micro-solid phase extraction (μ-SPE), indicating its remarkable preconcentration ability. Furthermore, the adsorption amounts by HL-COP μ-SPE were 1.0-11.0 folds as those by three commonly used commercial adsorbents. Then, HL-COP was applied as adsorbent of online μ-SPE coupled with high performance liquid chromatography (HPLC) for enrichment and analysis of trace Sudan dyes in food samples with detection limit of 0.03-0.15μg/L. The method was successfully applied for online analysis of chilli powder and sausage samples. Sudan II and Sudan III in one positive chilli powder sample were actually found and determined with concentrations of 8.3 and 6.8μg/kg, respectively. The recoveries of chilli powder and sausage samples were in range of 75.8-108.2% and 73.8-112.6% with relative standard deviations of 1.2-8.5% and 1.9-9.4% (n=5), respectively. The proposed method was accurate, reliable and convenient for the online simultaneous analysis of trace Sudan dyes in food samples.

  8. Subcellular localization and antiviral activity of carminic acid/poly r(A-U) combinations.

    PubMed

    Krabill, K; Jamison, J M; Gilloteaux, J; Summers, J L

    1993-10-01

    Carminic acid (CAR) enhances the antiviral activity of poly r(A-U) twelve-fold without increasing interferon induction, inactivating the vesicular stomatitis virus or inducing host cell cytotoxicity. Phase contrast photomicrographs of human foreskin fibroblasts (HSF) incubated with CAR alone, poly r(A-U) alone or with a CAR/poly r(A-U) combination illustrate that the CAR/poly r(A-U) combinations display altered subcellular distribution with the CAR being localized in the nucleoli and chromatin. Phase contrast and fluorescence photomicrographs of adriamycin (ADR)-treated and ADR/poly r(A-U)-treated HSF cells corroborate these findings. These results suggest that modulation of one or more nucleolar processes may be responsible for the enhanced antiviral activity. PMID:8287022

  9. Vibrational spectroscopy to study degradation of natural dyes. Assessment of oxygen-free cassette for safe exposition of artefacts.

    PubMed

    Koperska, Monika; Łojewski, Tomasz; Łojewska, Joanna

    2011-03-01

    An important issue connected with conservation chemistry is how to improve the storage and exposure conditions in order to suppress the fading and degradation of dyes and other components of paintings. Although the oxygen-free exposure cassettes are commonly known in museums, there is still lack of information in the literature about the effect of anoxic conditions on the degradation of dyes. This study is an attempt to start a database formation on the dyes degradation. Five commercial dyes (indigo, dragon's blood, curcumin, madder, carminic acid) were submitted to accelerated ageing by exposure to intensive light in the visible range in both oxygen-free (anoxia) and -rich conditions. Degradation of the samples was investigated by several analytical techniques (attenuated total reflectance infrared spectroscopy, Raman spectroscopy, reflectance UV-Vis spectroscopy, X-ray fluorescence spectroscopy and optical microscopy). The conclusions are based on the estimators (derived from the determination of colour differences from Vis spectra and from the changes in FTIR and Raman vibrational bands intensity). According to them, only indigo, dragon's blood and curcumin show greater stability in anoxic conditions in comparison with oxygen-rich ones while madder, carminic acid undergo greater degradation. PMID:21165610

  10. Influence of the Terminal Electron Donor in D-D-π-A Organic Dye-Sensitized Solar Cells: Dithieno[3,2-b:2',3'-d]pyrrole versus Bis(amine).

    PubMed

    Dai, Panpan; Yang, Lin; Liang, Mao; Dong, Huanhuan; Wang, Peng; Zhang, Chunyao; Sun, Zhe; Xue, Song

    2015-10-14

    With respect to the electron-withdrawing acceptors of D-A-π-A organic dyes, reports on the second electron-donating donors for D-D-π-A organic dyes are very limited. Both of the dyes have attracted significant attention in the field of dye-sensitized solar cells (DSCs). In this work, four new D-D-π-A organic dyes with dithieno[3,2-b:2',3'-d]pyrrole (DTP) or bis(amine) donor have been designed and synthesized for a investigation of the influence of the terminal electron donor in D-D-π-A organic dye-sensitized solar cells. It is found that DTP is a promising building block as the terminal electron donor when introduced in the dithiophenepyrrole direction, but not just a good bridge, which exhibits several characteristics: (i) efficiently increasing the maximum molar absorption coefficient and extending the absorption bands; (ii) showing stronger charge transfer interaction as compared with the pyrrole direction; (iii) beneficial to photocurrent generation of DSCs employing cobalt electrolytes. DSCs based on M45 with the Co-phen electrolyte exhibit good light-to-electric energy conversion efficiencies as high as 9.02%, with a short circuit current density (JSC) of 15.3 mA cm(-2), open circuit voltage (VOC) of 867 mV and fill factor (FF) of 0.68 under AM 1.5 illumination (100 mW cm(-2)). The results demonstrate that N,S-heterocycles such as DTP unit could be promising candidates for application in highly efficient DSCs employing cobalt electrolyte.

  11. Influence of the Terminal Electron Donor in D-D-π-A Organic Dye-Sensitized Solar Cells: Dithieno[3,2-b:2',3'-d]pyrrole versus Bis(amine).

    PubMed

    Dai, Panpan; Yang, Lin; Liang, Mao; Dong, Huanhuan; Wang, Peng; Zhang, Chunyao; Sun, Zhe; Xue, Song

    2015-10-14

    With respect to the electron-withdrawing acceptors of D-A-π-A organic dyes, reports on the second electron-donating donors for D-D-π-A organic dyes are very limited. Both of the dyes have attracted significant attention in the field of dye-sensitized solar cells (DSCs). In this work, four new D-D-π-A organic dyes with dithieno[3,2-b:2',3'-d]pyrrole (DTP) or bis(amine) donor have been designed and synthesized for a investigation of the influence of the terminal electron donor in D-D-π-A organic dye-sensitized solar cells. It is found that DTP is a promising building block as the terminal electron donor when introduced in the dithiophenepyrrole direction, but not just a good bridge, which exhibits several characteristics: (i) efficiently increasing the maximum molar absorption coefficient and extending the absorption bands; (ii) showing stronger charge transfer interaction as compared with the pyrrole direction; (iii) beneficial to photocurrent generation of DSCs employing cobalt electrolytes. DSCs based on M45 with the Co-phen electrolyte exhibit good light-to-electric energy conversion efficiencies as high as 9.02%, with a short circuit current density (JSC) of 15.3 mA cm(-2), open circuit voltage (VOC) of 867 mV and fill factor (FF) of 0.68 under AM 1.5 illumination (100 mW cm(-2)). The results demonstrate that N,S-heterocycles such as DTP unit could be promising candidates for application in highly efficient DSCs employing cobalt electrolyte. PMID:26394089

  12. Identification and characterization of artists' red dyes and their mixtures by surface-enhanced Raman spectroscopy.

    PubMed

    Whitney, Alyson V; Casadio, Francesca; Van Duyne, Richard P

    2007-09-01

    Silver film over nanospheres (AgFONs) were successfully employed as surface-enhanced Raman spectroscopy (SERS) substrates to characterize several artists' red dyes including: alizarin, purpurin, carminic acid, cochineal, and lac dye. Spectra were collected on sample volumes (1 x 10(-6) M or 15 ng/microL) similar to those that would be found in a museum setting and were found to be higher in resolution and consistency than those collected on silver island films (AgIFs). In fact, to the best of the authors' knowledge, this work presents the highest resolution spectrum of the artists' material cochineal to date. In order to determine an optimized SERS system for dye identification, experiments were conducted in which laser excitation wavelengths were matched with correlating AgFON localized surface plasmon resonance (LSPR) maxima. Enhancements of approximately two orders of magnitude were seen when resonance SERS conditions were met in comparison to non-resonance SERS conditions. Finally, because most samples collected in a museum contain multiple dyestuffs, AgFONs were employed to simultaneously identify individual dyes within several dye mixtures. These results indicate that AgFONs have great potential to be used to identify not only real artwork samples containing a single dye but also samples containing dyes mixtures. PMID:17910797

  13. High-efficiency sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays

    NASA Astrophysics Data System (ADS)

    Guo, Xiao; Fu, Yongming; Hong, Deyi; Yu, Binwei; He, Haoxuan; Wang, Qiang; Xing, Lili; Xue, Xinyu

    2016-09-01

    Highly-efficient sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays was achieved. A steel screen was used as the substrate for supporting FeS/ZnO nanoarrays, and the nanoarrays were vertically and uniformly grown on the substrate via a wet-chemical route. Under ultrasonic and solar irradiation, FeS/ZnO nanoarrays have high sono-photocatalytic activity for degrading methylene blue in water. The photogenerated carriers can be separated by a piezoelectric field and a built-in electric field, resulting in a low recombination rate and high photocatalytic efficiency. The piezophototronic and photocatalytic effects were coupled together. The experimental/theoretical data indicate that this novel wastewater treatment can co-use mechanical and solar energy in nature, and so is a promising technology for environment improvement.

  14. CTAB-assisted synthesis of novel ultrathin MoSe2 nanosheets perpendicular to graphene for the adsorption and photodegradation of organic dyes under visible light.

    PubMed

    Wu, Yuxin; Xu, Mingquan; Chen, Xi; Yang, Shuanglei; Wu, Hanshuo; Pan, Jun; Xiong, Xiang

    2016-01-01

    A novel nanostructure of perpendicular ultrathin MoSe2 nanosheets directly grown on graphene was produced by a facile hydrothermal method in the presence of CTAB. The vertically-oriented and ultrathin MoSe2 nanosheets distribute uniformly on the surface of graphene, and the nanosheets are typically 2-3 layers, which is confirmed by TEM and red shift of the A1g Raman peak. In comparison with pure MoSe2 and MoSe2 nanospheres on graphene, vertically oriented MoSe2 nanosheets on graphene show enhanced organic dye adsorption ability and photocatalytic performance in the degradation of MB, RhB and MO under dark conditions and visible light irradiation. The excellent photocatalytic activity may be contributed by the unique perpendicular MoSe2 nanosheets with fully exposed active edges and hybridized with graphene for reduced electron-hole pair recombination. PMID:26627597

  15. Investigation of energy transfer and charge trapping in dye-doped organic light-emitting diodes by magneto-electroluminescence measurement

    NASA Astrophysics Data System (ADS)

    Peng, Qiming; Gao, Na; Li, Weijun; Chen, Ping; Li, Feng; Ma, Yuguang

    2013-05-01

    We investigated the energy transfer and charge trapping (CT) in dye-doped organic light-emitting devices by using the magneto-electroluminescence as a tool. An intra-molecular charge-transfer fluorescent material N,N-diphenyl-4-(9-phenylnaphtho-[2,3-c][1,2,5]thiadiazol-4-yl)aniline was selected as the guest emitter. The tri-(8-hydroxyquinoline)-aluminum and 1,3-bis(9-carbazolyl)benzene were selected as the hosts. Our results demonstrate that as the energy difference between the HOMO (highest occupied molecular orbital)/LUMO (lowest unoccupied molecular orbital) of the host and the guest (ΔEHOMO/ΔELUMO) increases, the CT becomes more dominant, and the CT cannot be ignored even when the ΔEHOMO/ΔELUMO is small and the emission spectrum of the host overlaps the absorption spectrum of the guest well.

  16. Circularly polarized luminescence by visible-light absorption in a chiral O-BODIPY dye: unprecedented design of CPL organic molecules from achiral chromophores.

    PubMed

    Sánchez-Carnerero, Esther M; Moreno, Florencio; Maroto, Beatriz L; Agarrabeitia, Antonia R; Ortiz, María J; Vo, Bryan G; Muller, Gilles; de la Moya, Santiago

    2014-03-01

    Circularly polarized luminescence (CPL) in simple (small, nonaggregated, nonpolymeric) O-BODIPYs (R)-1 and (S)-1 by irradiation with visible light is first detected as proof of the ability of a new structural design to achieve CPL from inherently achiral monochromophore systems in simple organic molecules. The measured level of CPL (|g(lum)|) in solution falls into the usual range of that obtained from other simple organic molecules (10(-5)-10(-2) range), but the latter having more complex architectures since axially chiral chromophores or multichromophore systems are usually required. The new design is based on chirally perturbing the acting achiral chromophore by orthogonally tethering a single axially chiral 1,1'-binaphtyl moiety to it. The latter does not participate as a chromophore in the light-absorption/emission phenomenon. This simple design opens up new perspectives for the future development of new small-sized CPL organic dyes (e.g., those based on other highly luminescent achiral chromophores and/or chirally perturbing moieties), as well as for the improvement of the CPL properties of the organic molecules spanning their use in photonic applications.

  17. Adsorption of porphyrin and carminic acid on TiO2 nanoparticles: A photo-active nano-hybrid material for hybrid bulk heterojunction solar cells.

    PubMed

    Munir, Shamsa; Shah, Syed Mujtaba; Hussain, Hazrat; Siddiq, Muhammad

    2015-12-01

    A photo-active nano-hybrid material consisting of titania nanoparticles, carminic acid, and sulphonic acid functionalized porphyrin is reported here. In an attempt to extend the absorption spectrum of titania to visible region by co-adsorbing carminic acid and sulphonic acid functionalized porphyrin on its surface. Interesting changes in the UV-visible and fluorescence spectra were noticed. The adsorption of carminic acid resulted in the formation of charge transfer complex with titania nanoparticles. This was confirmed by the electronic absorption and fluorescence emission spectroscopies. Chemisorption of porphyrin on the carminic acid functionalized titania further boosted the charge transfer effect. This was noticed by the increase in intensity and width of the charge transfer absorption and emission bands. Energy level diagram showed that the interaction among the constituents of the nano-hybrid assembly permitted the flow of electron in a cascade manner from carminic acid to TiO2.This also allowed direct flow of electrons either from carminic acid or porphyrin toward titania. The material was used as an active blend in hybrid bulk heterojunction solar cells. Co-functionalized TiO2-based devices were found 3.5 times more efficient than the reference device but morphology of the device proved a major setback. PMID:26555643

  18. Adsorption of porphyrin and carminic acid on TiO2 nanoparticles: A photo-active nano-hybrid material for hybrid bulk heterojunction solar cells.

    PubMed

    Munir, Shamsa; Shah, Syed Mujtaba; Hussain, Hazrat; Siddiq, Muhammad

    2015-12-01

    A photo-active nano-hybrid material consisting of titania nanoparticles, carminic acid, and sulphonic acid functionalized porphyrin is reported here. In an attempt to extend the absorption spectrum of titania to visible region by co-adsorbing carminic acid and sulphonic acid functionalized porphyrin on its surface. Interesting changes in the UV-visible and fluorescence spectra were noticed. The adsorption of carminic acid resulted in the formation of charge transfer complex with titania nanoparticles. This was confirmed by the electronic absorption and fluorescence emission spectroscopies. Chemisorption of porphyrin on the carminic acid functionalized titania further boosted the charge transfer effect. This was noticed by the increase in intensity and width of the charge transfer absorption and emission bands. Energy level diagram showed that the interaction among the constituents of the nano-hybrid assembly permitted the flow of electron in a cascade manner from carminic acid to TiO2.This also allowed direct flow of electrons either from carminic acid or porphyrin toward titania. The material was used as an active blend in hybrid bulk heterojunction solar cells. Co-functionalized TiO2-based devices were found 3.5 times more efficient than the reference device but morphology of the device proved a major setback.

  19. Enhanced Electron Lifetimes in Dye-Sensitized Solar Cells Using a Dichromophoric Porphyrin: The Utility of Intermolecular Forces.

    PubMed

    Zhao, Long; Wagner, Pawel; van der Salm, Holly; Gordon, Keith C; Mori, Shogo; Mozer, Attila J

    2015-10-01

    Electron lifetimes in dye-sensitized solar cells employing a porphyrin dye, an organic dye, a 1:1 mixture of the two dyes, and a dichromophoric dye design consisting of the two dyes using a nonconjugated linker were measured, suggesting that the dispersion force of the organic dyes has a significant detrimental effect on the electron lifetime and that the dichromophoric design can be utilized to control the effect of the dispersion force.

  20. Synthesis of Tunable Band Gap Semiconductor Nickel Sulphide Nanoparticles: Rapid and Round the Clock Degradation of Organic Dyes

    NASA Astrophysics Data System (ADS)

    Molla, Aniruddha; Sahu, Meenakshi; Hussain, Sahid

    2016-05-01

    Controlled shape and size with tuneable band gap (1.92–2.41 eV), nickel sulphide NPs was achieved in presence of thiourea or thioacetamide as sulphur sources with the variations of temperature and capping agents. Synthesized NPs were fully characterized by powder XRD, IR, UV-vis, DRS, FE-SEM, TEM, EDX, XPS, TGA and BET. Capping agent, temperature and sulphur sources have significant role in controlling the band gaps, morphology and surface area of NPs. The catalytic activities of NPs were tested for round the clock (light and dark) decomposition of crystal violet (CV), rhodamine B (RhB), methylene blue (MB), nile blue (NB) and eriochrome black T (EBT). Agitation speed, temperature, pH and ionic strength have significant role on its catalytic activities. The catalyst was found to generate reactive oxygen species (ROS) both in presence and absence of light which is responsible for the decomposition of dyes into small fractions, identified with ESI-mass spectra.

  1. Fe3 O4 Anisotropic Nanostructures in Hydrogels: Efficient Catalysts for the Rapid Removal of Organic Dyes from Wastewater.

    PubMed

    Gao, Yang; Hu, Chen; Zheng, Wen Jiang; Yang, Sen; Li, Fei; Sun, Shao Dong; Zrínyi, Miklós; Osada, Yoshihito; Yang, Zhi Mao; Chen, Yong Mei

    2016-07-01

    Fe3 O4 anisotropic nanostructures that exhibit excellent catalytic performance are rarely used to catalyze Fenton-like reactions because of the inevitable drawbacks resulting from traditional preparation methods. In this study, a facile, nontoxic, water-based approach is developed for directly regulating a series of anisotropic morphologies of Fe3 O4 nanostructures in a hydrogel matrix. In having the advantages of both the catalytic activity of Fe3 O4 and the adsorptive capacity of an anionic polymer network, the hybrid nanocomposites have the capability to effect the rapid removal of cationic dyes, such as methylene blue, from water samples. Perhaps more interestingly, hybrid nanocomposites loaded with Fe3 O4 nanorods exhibit the highest catalytic activity compared to those composed of nanoneedles and nanooctahedra, revealing the important role of nanostructure morphology. By means of scanning electrochemical microscopy, it is revealed that Fe3 O4 nanorods can efficiently catalyze H2 O2 decomposition and thus generate more free radicals ((.) OH, (.) HO2 ) for methylene blue degradation, which might account for their high catalytic activity.

  2. Fe3 O4 Anisotropic Nanostructures in Hydrogels: Efficient Catalysts for the Rapid Removal of Organic Dyes from Wastewater.

    PubMed

    Gao, Yang; Hu, Chen; Zheng, Wen Jiang; Yang, Sen; Li, Fei; Sun, Shao Dong; Zrínyi, Miklós; Osada, Yoshihito; Yang, Zhi Mao; Chen, Yong Mei

    2016-07-01

    Fe3 O4 anisotropic nanostructures that exhibit excellent catalytic performance are rarely used to catalyze Fenton-like reactions because of the inevitable drawbacks resulting from traditional preparation methods. In this study, a facile, nontoxic, water-based approach is developed for directly regulating a series of anisotropic morphologies of Fe3 O4 nanostructures in a hydrogel matrix. In having the advantages of both the catalytic activity of Fe3 O4 and the adsorptive capacity of an anionic polymer network, the hybrid nanocomposites have the capability to effect the rapid removal of cationic dyes, such as methylene blue, from water samples. Perhaps more interestingly, hybrid nanocomposites loaded with Fe3 O4 nanorods exhibit the highest catalytic activity compared to those composed of nanoneedles and nanooctahedra, revealing the important role of nanostructure morphology. By means of scanning electrochemical microscopy, it is revealed that Fe3 O4 nanorods can efficiently catalyze H2 O2 decomposition and thus generate more free radicals ((.) OH, (.) HO2 ) for methylene blue degradation, which might account for their high catalytic activity. PMID:26955896

  3. Synthesis of Tunable Band Gap Semiconductor Nickel Sulphide Nanoparticles: Rapid and Round the Clock Degradation of Organic Dyes

    PubMed Central

    Molla, Aniruddha; Sahu, Meenakshi; Hussain, Sahid

    2016-01-01

    Controlled shape and size with tuneable band gap (1.92–2.41 eV), nickel sulphide NPs was achieved in presence of thiourea or thioacetamide as sulphur sources with the variations of temperature and capping agents. Synthesized NPs were fully characterized by powder XRD, IR, UV-vis, DRS, FE-SEM, TEM, EDX, XPS, TGA and BET. Capping agent, temperature and sulphur sources have significant role in controlling the band gaps, morphology and surface area of NPs. The catalytic activities of NPs were tested for round the clock (light and dark) decomposition of crystal violet (CV), rhodamine B (RhB), methylene blue (MB), nile blue (NB) and eriochrome black T (EBT). Agitation speed, temperature, pH and ionic strength have significant role on its catalytic activities. The catalyst was found to generate reactive oxygen species (ROS) both in presence and absence of light which is responsible for the decomposition of dyes into small fractions, identified with ESI-mass spectra. PMID:27185051

  4. Aegle marmelos Mediated Green Synthesis of Different Nanostructured Metal Hexacyanoferrates: Activity against Photodegradation of Harmful Organic Dyes.

    PubMed

    Jassal, Vidhisha; Shanker, Uma; Kaith, B S

    2016-01-01

    Prussian blue analogue potassium metal hexacyanoferrate (KMHCF) nanoparticles Fe4[Fe(CN)6]3 (FeHCF), K2Cu3[Fe(CN)6]2 (KCuHCF), K2Ni[Fe(CN)6]·3H2O (KNiHCF), and K2Co[Fe(CN)6] (KCoHCF) have been synthesized using plant based biosurfactant Aegle marmelos (Bael) and water as a green solvent. It must be emphasized here that no harmful reagent or solvent was used throughout the study. Plant extracts are easily biodegradable and therefore do not cause any harm to the environment. Hence, the proposed method of synthesis of various KMHCF nanoparticles followed a green path. The synthesized nanoparticles were characterized by powder X-ray diffraction (PXRD), Field-Emission Scanning Electron Microscopy (FE-SEM), Transmission Electron Microscopy (TEM), and Fourier Transform Infrared Spectroscopy (FT-IR). MHCF nanoparticles were used for the photocatalytic degradation of toxic dyes like Malachite Green (MG), Eriochrome Black T (EBT), Methyl Orange (MO), and Methylene Blue (MB). Under optimized reaction conditions, maximum photocatalytic degradation was achieved in case of KCuHCF nanoparticles mediated degradation process (MG: 96.06%, EBT: 83.03%, MB: 94.72%, and MO: 63.71%) followed by KNiHCF (MG: 95%, EBT: 80.32%, MB: 91.35%, and MO: 59.42%), KCoHCF (MG: 91.45%, EBT: 78.84%, MB: 89.28%, and MO: 58.20%). PMID:27034896

  5. Aegle marmelos Mediated Green Synthesis of Different Nanostructured Metal Hexacyanoferrates: Activity against Photodegradation of Harmful Organic Dyes

    PubMed Central

    Jassal, Vidhisha; Kaith, B. S.

    2016-01-01

    Prussian blue analogue potassium metal hexacyanoferrate (KMHCF) nanoparticles Fe4[Fe(CN)6]3 (FeHCF), K2Cu3[Fe(CN)6]2 (KCuHCF), K2Ni[Fe(CN)6]·3H2O (KNiHCF), and K2Co[Fe(CN)6] (KCoHCF) have been synthesized using plant based biosurfactant Aegle marmelos (Bael) and water as a green solvent. It must be emphasized here that no harmful reagent or solvent was used throughout the study. Plant extracts are easily biodegradable and therefore do not cause any harm to the environment. Hence, the proposed method of synthesis of various KMHCF nanoparticles followed a green path. The synthesized nanoparticles were characterized by powder X-ray diffraction (PXRD), Field-Emission Scanning Electron Microscopy (FE-SEM), Transmission Electron Microscopy (TEM), and Fourier Transform Infrared Spectroscopy (FT-IR). MHCF nanoparticles were used for the photocatalytic degradation of toxic dyes like Malachite Green (MG), Eriochrome Black T (EBT), Methyl Orange (MO), and Methylene Blue (MB). Under optimized reaction conditions, maximum photocatalytic degradation was achieved in case of KCuHCF nanoparticles mediated degradation process (MG: 96.06%, EBT: 83.03%, MB: 94.72%, and MO: 63.71%) followed by KNiHCF (MG: 95%, EBT: 80.32%, MB: 91.35%, and MO: 59.42%), KCoHCF (MG: 91.45%, EBT: 78.84%, MB: 89.28%, and MO: 58.20%). PMID:27034896

  6. Synthesis of Tunable Band Gap Semiconductor Nickel Sulphide Nanoparticles: Rapid and Round the Clock Degradation of Organic Dyes

    NASA Astrophysics Data System (ADS)

    Molla, Aniruddha; Sahu, Meenakshi; Hussain, Sahid

    2016-05-01

    Controlled shape and size with tuneable band gap (1.92-2.41 eV), nickel sulphide NPs was achieved in presence of thiourea or thioacetamide as sulphur sources with the variations of temperature and capping agents. Synthesized NPs were fully characterized by powder XRD, IR, UV-vis, DRS, FE-SEM, TEM, EDX, XPS, TGA and BET. Capping agent, temperature and sulphur sources have significant role in controlling the band gaps, morphology and surface area of NPs. The catalytic activities of NPs were tested for round the clock (light and dark) decomposition of crystal violet (CV), rhodamine B (RhB), methylene blue (MB), nile blue (NB) and eriochrome black T (EBT). Agitation speed, temperature, pH and ionic strength have significant role on its catalytic activities. The catalyst was found to generate reactive oxygen species (ROS) both in presence and absence of light which is responsible for the decomposition of dyes into small fractions, identified with ESI-mass spectra.

  7. Transparent bifacial dye-sensitized solar cells based on organic counter electrodes and iodine-free electrolyte

    NASA Astrophysics Data System (ADS)

    Ku, Zhiliang; Rong, Yaoguang; Han, Hongwei

    2013-10-01

    In this study, a novel bifacially active transparent dye-sensitized solar cell (DSSCs) assembled with a transparent poly(3,4-ethylenedioxythiophene) (PEDOT) counter electrode and a colorless iodine-free polymer gel (IFPG) electrolyte was developed. The IFPG electrolyte was prepared by employing an ionic liquid (1,2-dimethyl-3-propylinmidazolium iodide, DMPII) as the charge transfer intermediate and a polymer composite as the gelator without the addition of iodine, exhibiting high conductivity and non-absorption characters. PEDOT electrodes were prepared via a facile electro-polymerization method. By controlling the amount of polymerization charge capacity, we optimized the PEDOT electrodes with high transparency and a favorable activity for catalyzing the IFPG electrolyte. The bifacial DSSCs device fabricated by this kind of transparent PEDOT electrode and colorless IFPG electrolyte showed a power conversion efficiency (PCE) of 6.35% and 4.98% at 100 mW cm-2 AM1.5 illumination corresponding to front- and rear-side illumination. It is notable that the PCE under rear-side illumination approaches 80% that of front-side illumination. Moreover, the device shows excellent stability as confirmed by aging test. These promising results highlight the enormous potential of this transparent PEDOT CE and colorless IFPG electrolyte in scaling up and commercialization of low cost and effective bifacial DSSCs.

  8. Surface-enhanced Raman scattering study of organic pigments using silver and gold nanoparticles prepared by pulsed laser ablation

    NASA Astrophysics Data System (ADS)

    Fazio, E.; Trusso, S.; Ponterio, R. C.

    2013-05-01

    The identification of pigments used in ancient times represents an interesting task in order to discriminate a production of a precise geographic area or to trace out the ancient commercial networks. Conventional micro-Raman spectroscopy (MRS), being a non-destructiveness technique, has been largely used for the analysis of dyes. Nevertheless several pigments, especially of organic origin, show weak Raman activity beside a strong a fluorescence that prevents their identification. Surface enhanced Raman scattering (SERS) can address such difficulties. The presence of noble metal nanoparticles induces a giant amplification of the Raman signal beside the fluorescence quenching. In this work we present the use of gold and silver nanoparticles to enhance the Raman signal of some commercial red organic dyes: bazilwood, dragon's blood, carmine and madder lake. The nanoparticles were prepared adopting two approaches: (1) ablating metallic targets in water using a pulsed Nd:YAG laser at 532 nm and (2) depositing the nanoparticles on glass substrates by means of a KrF excimer laser ablation process, performed in a controlled argon atmosphere.

  9. The Acaricidal Activity of Venom from the Jellyfish Nemopilema nomurai against the Carmine Spider Mite Tetranychus cinnabarinus.

    PubMed

    Yu, Huahua; Yue, Yang; Dong, Xiangli; Li, Rongfeng; Li, Pengcheng

    2016-01-01

    The carmine spider mite Tetranychus cinnabarinus (T. cinnabarinus) is a common polyphagous pest that attacks crops, vegetables, flowers, and so on. It is necessary to find lead compounds for developing novel, powerful, and environmentally-friendly acaricides as an alternative approach to controlling the carmine spider mite because of the serious resistance and residual agrochemicals in the environment. In addition, the study on the acaricidal activities of marine bioactive substances is comparatively deficient. In the present study, the acaricidal activity of venom (NnFV) from the jellyfish Nemopilema nomurai against the carmine spider mite T. cinnabarinus was determined for the first time. The venom had contact toxicity, and the 24-h LC50-value was 29.1 μg/mL. The mite body wall was affected by the venom, with the mite body having no luster and being seriously shrunken after 24 h. T. cinnabarinus was a potential target pest of NnFV, which had potential as a type of natural bioacaricide. The repellent activity and systemic toxicity of the venom against T. cinnabarinus were also studied. However, NnFV had no repellent activity and systemic toxicity against T. cinnabarinus. PMID:27294957

  10. Spectrophotometric determination of nitrite based on its catalytic effect on the oxidation of carminic acid by bromate.

    PubMed

    Manzoori, J L; Sorouraddin, M H; Haji-Shabani, A M

    1998-08-01

    A highly sensitive and selective method is described for the determination of trace amounts of nitrite based on its effect on the oxidation of carminic acid with bromate. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of carminic acid at 490 nm after 3 min of mixing the reagents. The optimum reaction conditions were 1.8x10(-1) mol l(-1) H(2)SO(4), 3.8x10(-3) mol l(-1) KBrO(3), and 1.2x10(-4) mol l(-1) carminic acid at 30 degrees C. By using the recommended procedure, the calibration graph was linear from 0.2 to 14 ng ml(-1) of nitrite; the detection limit was 0.04 ng ml(-1); the R.S.D. for six replicate determinations of 6 ng ml(-1) was 1.7%. The method is mostly free from interference, especially from large amounts of nitrate and ammonium ions. The proposed method was applied to the determination of nitrite in rain and river water. PMID:18967267

  11. Spectrophotometric determination of osmium based on its catalytic effect on the oxidation of carminic acid by hydrogen peroxide.

    PubMed

    Manzoori, J L; Sorouraddin, M H; Amjadi, M

    2000-10-01

    A highly sensitive spectrophotometric method is described for the determination of trace amounts of osmium(VIII), based on its catalytic effect on the oxidation of carminic acid by hydrogen peroxide. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of carminic acid at 540 nm after 3 min of mixing the reagents. The optimum reaction conditions were 1x10(-4) mol l(-1) carminic acid, 0.013 mol l(-1) hydrogen peroxide and pH 10 at 25 degrees C. By using the recommended procedure, the calibration graph was linear from 0.1 to 1.5 ng ml(-1) of osmium; the detection limit was 0.02 ng ml(-1); the RSD for five replicate determinations of 0.2-1.4 ng ml(-1) was in the range of 1.8-4.7%. The influence of several foreign ions on osmium determination were studied and the effect of interfering ions were removed by extracting osmium into isobuthyl methyl ketone and back extracting into sodium hydroxide solution. PMID:18968089

  12. The Acaricidal Activity of Venom from the Jellyfish Nemopilema nomurai against the Carmine Spider Mite Tetranychus cinnabarinus.

    PubMed

    Yu, Huahua; Yue, Yang; Dong, Xiangli; Li, Rongfeng; Li, Pengcheng

    2016-06-09

    The carmine spider mite Tetranychus cinnabarinus (T. cinnabarinus) is a common polyphagous pest that attacks crops, vegetables, flowers, and so on. It is necessary to find lead compounds for developing novel, powerful, and environmentally-friendly acaricides as an alternative approach to controlling the carmine spider mite because of the serious resistance and residual agrochemicals in the environment. In addition, the study on the acaricidal activities of marine bioactive substances is comparatively deficient. In the present study, the acaricidal activity of venom (NnFV) from the jellyfish Nemopilema nomurai against the carmine spider mite T. cinnabarinus was determined for the first time. The venom had contact toxicity, and the 24-h LC50-value was 29.1 μg/mL. The mite body wall was affected by the venom, with the mite body having no luster and being seriously shrunken after 24 h. T. cinnabarinus was a potential target pest of NnFV, which had potential as a type of natural bioacaricide. The repellent activity and systemic toxicity of the venom against T. cinnabarinus were also studied. However, NnFV had no repellent activity and systemic toxicity against T. cinnabarinus.

  13. Spectrophotometric determination of nitrite based on its catalytic effect on the oxidation of carminic acid by bromate.

    PubMed

    Manzoori, J L; Sorouraddin, M H; Haji-Shabani, A M

    1998-08-01

    A highly sensitive and selective method is described for the determination of trace amounts of nitrite based on its effect on the oxidation of carminic acid with bromate. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of carminic acid at 490 nm after 3 min of mixing the reagents. The optimum reaction conditions were 1.8x10(-1) mol l(-1) H(2)SO(4), 3.8x10(-3) mol l(-1) KBrO(3), and 1.2x10(-4) mol l(-1) carminic acid at 30 degrees C. By using the recommended procedure, the calibration graph was linear from 0.2 to 14 ng ml(-1) of nitrite; the detection limit was 0.04 ng ml(-1); the R.S.D. for six replicate determinations of 6 ng ml(-1) was 1.7%. The method is mostly free from interference, especially from large amounts of nitrate and ammonium ions. The proposed method was applied to the determination of nitrite in rain and river water.

  14. The Acaricidal Activity of Venom from the Jellyfish Nemopilema nomurai against the Carmine Spider Mite Tetranychus cinnabarinus

    PubMed Central

    Yu, Huahua; Yue, Yang; Dong, Xiangli; Li, Rongfeng; Li, Pengcheng

    2016-01-01

    The carmine spider mite Tetranychus cinnabarinus (T. cinnabarinus) is a common polyphagous pest that attacks crops, vegetables, flowers, and so on. It is necessary to find lead compounds for developing novel, powerful, and environmentally-friendly acaricides as an alternative approach to controlling the carmine spider mite because of the serious resistance and residual agrochemicals in the environment. In addition, the study on the acaricidal activities of marine bioactive substances is comparatively deficient. In the present study, the acaricidal activity of venom (NnFV) from the jellyfish Nemopilema nomurai against the carmine spider mite T. cinnabarinus was determined for the first time. The venom had contact toxicity, and the 24-h LC50-value was 29.1 μg/mL. The mite body wall was affected by the venom, with the mite body having no luster and being seriously shrunken after 24 h. T. cinnabarinus was a potential target pest of NnFV, which had potential as a type of natural bioacaricide. The repellent activity and systemic toxicity of the venom against T. cinnabarinus were also studied. However, NnFV had no repellent activity and systemic toxicity against T. cinnabarinus. PMID:27294957

  15. Simultaneous identification of natural dyes in the collection of drawings and maps from The Royal Chancellery Archives in Granada (Spain) by CE.

    PubMed

    López-Montes, Ana; Blanc García, Rosario; Espejo, Teresa; Huertas-Perez, José F; Navalón, Alberto; Vílchez, José Luis

    2007-04-01

    A simple and rapid capillary electrophoretic method with UV detection (CE-UV) has been developed for the identification of five natural dyes namely, carmine, indigo, saffron, gamboge and Rubia tinctoria root. The separation was performed in a fused-silica capillary of 64.5 cm length and 50 microm id. The running buffer was 40 mM sodium tetraborate buffer solution (pH 9.25). The applied potential was 30 kV, the temperature was 25 degrees C and detections were performed at 196, 232, 252, 300 and 356 nm. The injections were under pressure of 50 mbar during 13 s. The method was applied to the identification of carminic acid, gambogic acid, crocetin, indigotin, alizarin and purpurin in the collection of drawings and maps at the Royal Chancellery Archives in Granada (Spain). The method was validated by using HPLC as a reference method. PMID:17366480

  16. Use of novel nest boxes by carmine bee-eaters (Merops nubicus) in captivity.

    PubMed

    Elston, Jennifer J; Carney, Jennifer; Quinones, Glorieli; Sky, Christy; Plasse, Chelle; Bettinger, Tammie

    2007-01-01

    Carmine bee-eaters make attractive additions to zoo aviaries but breeding programs have had challenges and limited success. The objectives of this study were to document nesting behavior of Carmine bee-eaters in a captive setting and compare reproductive success between a novel nest box (plastic, 17 x 30 x 22 cm) and a PVC pipe model used previously (30 cm long, 8 cm in diameter). Three bee-eater pairs were given access to seven nest chambers (six novel boxes, one PVC model). Behavioral observations occurred during a 15-min period in the morning or afternoon before egg production and continued until chicks fledged for a total of 87 observation periods (21.75 hr). All occurrences by an individual bird entering or exiting a nest tunnel, food provision, and the time (min) spent inside a nest cavity were documented. Additionally, daily temperature within each nest chamber was recorded. Before eggs were produced the average daily temperature (23.02 degrees C) within the nest chambers did not differ, suggesting that nest cavity choice was not influenced by temperature. No differences were detected among pairs in percent of observed time spent inside their nest cavities or number of times a nest tunnel was entered during the incubation or fledging periods. During incubation females spent a greater percent of observed time inside the nest cavity than males (P=0.02). During the fledging period food provision did not differ between the pairs, however males entered their nest tunnels more often per hour than females (P=0.03), and males tended to provide food more often than females (P=0.053). Two pairs nested in novel nest boxes and successfully fledged one chick each. The pair that nested in the PVC model did not fledge a chick. A nest box that aids in keeping eggs intact is essential for breeding bee-eaters in captivity, and maintaining captive populations will provide opportunities for zoo visitors to enjoy these birds and will reduce the need to remove birds from the wild

  17. Hierarchical Heteroaggregation of Binary Metal-Organic Gels with Tunable Porosity and Mixed Valence Metal Sites for Removal of Dyes in Water

    PubMed Central

    Mahmood, Asif; Xia, Wei; Mahmood, Nasir; Wang, Qingfei; Zou, Ruqiang

    2015-01-01

    Hierarchical heteronuclear metal-organic gels (MOGs) based on iron (Fe) and aluminium (Al) metal-organic framework (MOF) backbones bridged by tri-carboxylate ligands have firstly been synthesized by simple solvothermal method. Monometallic MOGs based on Fe or Al give homogenous monoliths, which have been tuned by introduction of heterogeneity in the system (mismatched growth). The developed gels demonstrate that surface areas, pore volumes and pore sizes can be readily tuned by optimizing heterogeneity. The work also elaborates effect of heterogeneity on size of MOG particles which increase substantially with increasing heterogeneity as well as obtaining mixed valence sites in the gels. High surface areas (1861 m2/g) and pore volumes (9.737 cc/g) were obtained for heterogeneous gels (0.5Fe-0.5Al). The large uptakes of dye molecules (290 mg/g rhodamine B and 265 mg/g methyl orange) with fast sorption kinetics in both neutral and acidic mediums show good stability and accessibility of MOG channels (micro and meso-/macropores), further demonstrating their potential applications in catalysis and sorption of large molecules. PMID:26014755

  18. A recyclable and highly active Co{sub 3}O{sub 4} nanoparticles/titanate nanowire catalyst for organic dyes degradation with peroxymonosulfate

    SciTech Connect

    Chen, Zhili; Chen, Shihua; Li, Yonghe; Si, Xiaolei; Huang, Jun; Massey, Sylvain; Chen, Guangliang

    2014-09-15

    Sodium ions of TNWs were exchanged with hydrogen ions, and this protocol was very suitable for capturing high density of cobalt ions. Meanwhile, the fabricated Co{sub 3}O{sub 4}/TNWs nano-material presented a highly catalytic and stable activity for dye degradation. - Highlights: • Co{sub 3}O{sub 4} nanoparticles were deposited on the pretreated TNWs surface. • The TNWs treated by hydrogen ions captures higher density of cobalt ions. • The Co{sub 3}O{sub 4}/TNWs catalyst possesses highly efficiency for dyes degradation with oxone. - Abstract: In this paper, we reported a recyclable and highly active porous catalyst of titanate nanowires (TNWs) coated with well-distributed Co{sub 3}O{sub 4} nanoparticles (NPs) (Co{sub 3}O{sub 4}/TNWs). Sodium ions of TNWs were exchanged with hydrogen ions in the dilute nitric acid, and this protocol was very suitable for capturing cobalt ions. X-ray diffraction (XRD) demonstrated the existence of Co{sub 3}O{sub 4} phase with unique lattice planes, such as (2 2 0), (3 1 1) and (5 1 1). Electron microscopes (FE-SEM and TEM) indicated that the Co{sub 3}O{sub 4} NPs with an average diameter of 22 ± 3 nm were coated uniformly on TNWs surface (average diameter: 37 ± 5.5 nm), and the Co{sub 3}O{sub 4} NPs mainly exposed their (2 2 0) and (2 2 2) active planes. XPS analysis confirms the formation of Co{sub 3}O{sub 4} phase by the presence of Co 2p peaks at 780.1 eV (2p 3/2) and 795.5 eV (2p 1/2). Methylene blue (MB) and other organic dyes (rhodamine B (RhB) and methyl orange (MO)) were chosen as target compounds for catalytic degradation under indoor scattering light. Compared to the original Co{sub 3}O{sub 4}/TNWs catalyst, the catalytic efficiency of nanoscaled catalyst with oxone for MB was about 15 times higher, and the MB solution (10 mg L{sup −1}) was completely degraded within 8 min. The catalytic activity of recycled catalyst used in the sixth run still remained very active, and the degradation time for MB was only 16 min

  19. In-tube electro-membrane extraction with a sub-microliter organic solvent consumption as an efficient technique for synthetic food dyes determination in foodstuff samples.

    PubMed

    Bazregar, Mohammad; Rajabi, Maryam; Yamini, Yadollah; Asghari, Alireza; Abdossalami asl, Yousef

    2015-09-01

    A simple and efficient extraction technique with a sub-microliter organic solvent consumption termed as in-tube electro-membrane extraction (IEME) is introduced. This method is based upon the electro-kinetic migration of ionized compounds by the application of an electrical potential difference. For this purpose, a thin polypropylene (PP) sheet placed inside a tube acts as a support for the membrane solvent, and 30μL of an aqueous acceptor solution is separated by this solvent from 1.2mL of an aqueous donor solution. This method yielded high extraction recoveries (63-81%), and the consumption of the organic solvent used was only 0.5μL. By performing this method, the purification is high, and the utilization of the organic solvent, used as a mediator, is very simple and repeatable. The proposed method was evaluated by extraction of four synthetic food dyes (Amaranth, Ponceau 4R, Allura Red, and Carmoisine) as the model analytes. Optimization of variables affecting the method was carried out in order to achieve the best extraction efficiency. These variables were the type of membrane solvent, applied extraction voltage, extraction time, pH range, and concentration of salt added. Under the optimized conditions, IEME-HPLC-UV provided a good linearity in the range of 1.00-800ngmL(-1), low limits of detection (0.3-1ngmL(-1)), and good extraction repeatabilities (RSDs below 5.2%, n=5). It seems that this design is a proper one for the automation of the method. Also the consumption of the organic solvent in a sub-microliter scale, and its simplicity, high efficiency, and high purification can help one getting closer to the objectives of the green chemistry. PMID:26256917

  20. In-tube electro-membrane extraction with a sub-microliter organic solvent consumption as an efficient technique for synthetic food dyes determination in foodstuff samples.

    PubMed

    Bazregar, Mohammad; Rajabi, Maryam; Yamini, Yadollah; Asghari, Alireza; Abdossalami asl, Yousef

    2015-09-01

    A simple and efficient extraction technique with a sub-microliter organic solvent consumption termed as in-tube electro-membrane extraction (IEME) is introduced. This method is based upon the electro-kinetic migration of ionized compounds by the application of an electrical potential difference. For this purpose, a thin polypropylene (PP) sheet placed inside a tube acts as a support for the membrane solvent, and 30μL of an aqueous acceptor solution is separated by this solvent from 1.2mL of an aqueous donor solution. This method yielded high extraction recoveries (63-81%), and the consumption of the organic solvent used was only 0.5μL. By performing this method, the purification is high, and the utilization of the organic solvent, used as a mediator, is very simple and repeatable. The proposed method was evaluated by extraction of four synthetic food dyes (Amaranth, Ponceau 4R, Allura Red, and Carmoisine) as the model analytes. Optimization of variables affecting the method was carried out in order to achieve the best extraction efficiency. These variables were the type of membrane solvent, applied extraction voltage, extraction time, pH range, and concentration of salt added. Under the optimized conditions, IEME-HPLC-UV provided a good linearity in the range of 1.00-800ngmL(-1), low limits of detection (0.3-1ngmL(-1)), and good extraction repeatabilities (RSDs below 5.2%, n=5). It seems that this design is a proper one for the automation of the method. Also the consumption of the organic solvent in a sub-microliter scale, and its simplicity, high efficiency, and high purification can help one getting closer to the objectives of the green chemistry.

  1. Allergic dermatoses and respiratory diseases from reactive dyes.

    PubMed

    Estlander, T

    1988-05-01

    5 cases of occupational eczema, urticaria and respiratory disease from reactive dyes, occurring during 1977-1987, are reported. The patients, 4 men and 1 woman, were 24-52 years old when examined. They had been working in dye houses or textile plants, and had been exposed to reactive dyes for 8 months to 4 years before symptoms developed. Only 1 of the patients has been able to continue in the same occupation. On patch testing, the 4 patients with eczema reacted positively to 9 commercial dye powders. 2 patients reacted to the same dye, Remazol Schwarz B. On scratch and/or prick testing, the 2 patients who also had respiratory symptoms and/or urticaria reacted positively to the same dyes as on patch testing. The 5th patient, who had urticaria and respiratory symptoms, reacted positively to a dye, Remazol Gold Gelb RNL, but the patch test with that dye was negative. None of the patients was patch-test-positive to para-phenylenediamine (PPD) or to textile dye allergens in a series of organic dyes. Thus, the series of organic dyes has little value in the screening of allergy to reactive dyes. A 1% pet. dilution of commercial dye powder for patch testing and the same concentration in distilled water for prick testing seem to be suitable for the screening of allergy to reactive dyes.

  2. Application of surface-enhanced Raman scattering (SERS) for the identification of anthraquinone dyes used in works of art

    SciTech Connect

    Chen, Kui; Leona, Marco; Yan, Fei; Wabuyele, Musundi B; Vo Dinh, Tuan

    2006-04-01

    Surface-enhanced Raman scattering (SERS) was investigated for applications in the analysis of anthraquinone dyes used in works of art. Two SERS procedures were developed and evaluated with three frequently used anthraquinone dyes, alizarin, carminic acid and lac dye. The first procedure involves coating a layer of silver nanoparticles directly on pieces of filter paper stained with the dyes of interest by thermal evaporation to induce SERS effect. In the second procedure, a SERS-active Ag-Al{sub 2}O{sub 3} substrate was prepared by spin-coating an alumina-nanoparticle layer onto a glass slide to provide the nanostructure of the substrate, followed by thermally evaporating a layer of silver nanoparticles on top of the alumina layer. Aliquots of dye solutions were delivered onto this substrate to be analyzed. Intense SERS spectra characteristic of alizarin, carminic acid and lac dye were obtained using both SERS procedures. The effects of two parameters, the concentration of the alumina suspension and the thickness of the silver nanoparticle layer on the performance of the Ag-Al{sub 2}O{sub 3} substrate were examined with alizarin as the model compound. Comparative studies were conducted between the Ag-Al{sub 2}O{sub 3} substrate and the SERS substrate prepared using Tollens reaction. The Ag-Al{sub 2}O{sub 3} substrate was shown to offer larger enhancement and improved reproducibility than the Tollens substrates. Finally, the potential applicability of the Ag-Al{sub 2}O{sub 3} substrate for the analysis of real artifact objects was illustrated by the identification of alizarin extracted from a small piece of textile dyed using traditional methods and materials. The limit of detection for alizarin was estimated to be 7 x 10{sup -15} g from tests performed on solutions of known concentration.

  3. A simple and rapid resonance Rayleigh scattering method for detection of indigo carmine in soft drink.

    PubMed

    Li, Qin; Yang, Jidong; Tan, Xuanping; Zhang, Zhan; Hu, Xiaomei; Yang, Menghuan

    2016-08-01

    A novel method that uses acridine orange (AO) to detect indigo carmine (IC) in soft drinks was developed. The method is highly sensitive and is based on a resonance Rayleigh scattering (RRS) technique. In Britton-Robinson (BR) buffer solution, pH 4.3, the weak RRS intensity of AO was greatly enhanced by the addition of IC, with the maximum peak located at 332 nm. Under optimum conditions, it was found that the enhanced RRS intensity was proportional to the concentration of IC over a range of 2-32 × 10(-6)  mol/L. A low detection limit of 2.4 × 10(-8)  mol/L was achieved. The sensitivity and selectivity of the method are high enough to permit the determination of trace amounts of IC without any significant interference from high levels of other components such as common anions and other amino acids. Finally, the concentration of IC in three different soft drinks was determined with satisfactory results. Copyright © 2016 John Wiley & Sons, Ltd. PMID:26791156

  4. Discoloration of Indigo Carmine Using Aqueous Extracts from Vegetables and Vegetable Residues as Enzyme Sources

    PubMed Central

    Solís, A.; Perea, F.; Solís, M.; Manjarrez, N.; Pérez, H. I.; Cassani, J.

    2013-01-01

    Several vegetables and vegetable residues were used as sources of enzymes capable to discolor indigo carmine (IC), completely or partially. Complete discoloration was achieved with aqueous extracts of green pea seeds and peels of green pea, cucumber, and kohlrabi, as well as spring onion leaves. The source of polyphenol oxidase (PPO), pH, time, and aeration is fundamental for the discoloration process catalyzed by PPO. The PPO present in the aqueous extract of green pea seeds was able to degrade 3,000 ppm of IC at a pH of 7.6 and magnetic stirring at 1,800 rpm in about 36 h. In addition, at 1,800 rpm and a pH of 7.6, this extract discolored 300 ppm of IC in 1:40 h; in the presence of 10% NaCl, the discoloration was complete in 5:50 h, whereas it was completed in 4:30 h with 5% NaCl and 2% laundry soap. PMID:24151588

  5. Discoloration of indigo carmine using aqueous extracts from vegetables and vegetable residues as enzyme sources.

    PubMed

    Solís, A; Perea, F; Solís, M; Manjarrez, N; Pérez, H I; Cassani, J

    2013-01-01

    Several vegetables and vegetable residues were used as sources of enzymes capable to discolor indigo carmine (IC), completely or partially. Complete discoloration was achieved with aqueous extracts of green pea seeds and peels of green pea, cucumber, and kohlrabi, as well as spring onion leaves. The source of polyphenol oxidase (PPO), pH, time, and aeration is fundamental for the discoloration process catalyzed by PPO. The PPO present in the aqueous extract of green pea seeds was able to degrade 3,000 ppm of IC at a pH of 7.6 and magnetic stirring at 1,800 rpm in about 36 h. In addition, at 1,800 rpm and a pH of 7.6, this extract discolored 300 ppm of IC in 1:40 h; in the presence of 10% NaCl, the discoloration was complete in 5:50 h, whereas it was completed in 4:30 h with 5% NaCl and 2% laundry soap. PMID:24151588

  6. Dyeing behaviour of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves (Lawsonia inermis)

    NASA Astrophysics Data System (ADS)

    Rehman, Fazal-ur; Adeel, Shahid; Qaiser, Summia; Ahmad Bhatti, Ijaz; Shahid, Muhammad; Zuber, Mohammad

    2012-11-01

    Dyeing behavior of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves has been investigated. Cotton and dye powder are irradiated to different absorbed doses of 2, 4, 6, 8 and 10 kGy using Cs-137 gamma irradiator. The dyeing parameters such as dyeing time, electrolyte (salt) concentration and mordant concentrations using copper and iron as mordants are optimized. Dyeing is performed using un-irradiated and irradiated cotton with dye solutions and their color strength values are evaluated in CIE Lab system using Spectraflash -SF650. Methods suggested by International Standard Organization (ISO) have been employed to investigate the colourfastness properties such as colourfastness to light, washing and rubbing of irradiated dyed fabric. It is found that gamma ray treatment of cotton dyed with extracts of henna leaves has significantly improved the color strength as well as enhanced the rating of fastness properties.

  7. Effect of organic solvents on J aggregation of pseudoisocyanine dye at mica/water interfaces: morphological transition from three-dimension to two-dimension.

    PubMed

    Yao, Hiroshi; Morita, Yoshinobu; Kimura, Keisaku

    2008-02-01

    Morphological and spectroscopic properties of pseudoisocyanine (PIC) J aggregates produced at mica/solution interfaces have been characterized by absorption/fluorescence spectroscopy, fluorescence microscopy, and atomic force microscopy. Addition of organic solvents (1-propanol (PrOH) or 1,4-dioxane (Dox)) into aqueous solutions of the PIC dye induced a transition of the morphology of the interfacial J aggregates. The characteristic feature of this transition is the thickness (or height) change of the aggregate domain layers from three-dimensions to two-dimensions: The domain area of the J aggregates was dependent on the amount of the organic cosolvent, while the domain thickness was dependent on the type of the cosolvent. In pure aqueous solution, the J aggregates at the mica/water interface had a three-dimensional structure with the height of approximately 3 nm (multilayer structure). In mixed solvents of PrOH/water or Dox/water (5 or 10 vol%), the interfacial aggregates became a bilayer or monolayer structure, respectively, assuming that PIC molecules are adsorbed on their molecular plane perpendicular to the mica surface. Meanwhile, optical properties (band width and peak position) of the J band were invariant upon addition of the organic cosolvents, suggesting that molecular packing in the J aggregates is essentially unchanged. These results revealed that spectroscopic properties of the interfacial PIC J aggregates were determined only by the lateral (two-dimensional) interaction within the adsorbed monolayer of PIC molecules on mica, and interlayer interaction in the multilayered J aggregate was consequently small. PMID:17963780

  8. An efficient photocatalyst for degradation of various organic dyes: Ag@Ag2MoO4-AgBr composite.

    PubMed

    Bai, Yu-Yang; Lu, Yi; Liu, Jin-Ku

    2016-04-15

    The Ag2MoO4-AgBr composite was prepared by a facile in-situ anion-exchange method, then the Ag nanoparticles were coated on this composite through photodeposition route to form a novel Ag@Ag2MoO4-AgBr composite. The in-situ Br(-) replacement in a crystal lattice node position of Ag2MoO4 crystal allows for overcoming the resistance of electron transition effectively. Meanwhile silver nano-particles on the surface of Ag@Ag2MoO4-AgBr composite could act as electron traps to intensify the photogeneration electron-hole separation and the subsequent transfer of the trapped electron to the adsorbed O2 as an electron acceptor. As an efficient visible light catalyst, the Ag@Ag2MoO4-AgBr composite exhibited superior photocatalytic activity for the degradation of various organic dyes. The experimental results demonstrated superior photocatalytic rate of Ag@Ag2MoO4-AgBr composite compared to pure AgBr and Ag2MoO4 crystals (37.6% and 348.4% enhancement respectively). The Ag@Ag2MoO4-AgBr composite cloud degraded Rhodamin B, bromophenol blue, and amino black 10b completed in 7min. PMID:26775100

  9. An efficient photocatalyst for degradation of various organic dyes: Ag@Ag2MoO4-AgBr composite.

    PubMed

    Bai, Yu-Yang; Lu, Yi; Liu, Jin-Ku

    2016-04-15

    The Ag2MoO4-AgBr composite was prepared by a facile in-situ anion-exchange method, then the Ag nanoparticles were coated on this composite through photodeposition route to form a novel Ag@Ag2MoO4-AgBr composite. The in-situ Br(-) replacement in a crystal lattice node position of Ag2MoO4 crystal allows for overcoming the resistance of electron transition effectively. Meanwhile silver nano-particles on the surface of Ag@Ag2MoO4-AgBr composite could act as electron traps to intensify the photogeneration electron-hole separation and the subsequent transfer of the trapped electron to the adsorbed O2 as an electron acceptor. As an efficient visible light catalyst, the Ag@Ag2MoO4-AgBr composite exhibited superior photocatalytic activity for the degradation of various organic dyes. The experimental results demonstrated superior photocatalytic rate of Ag@Ag2MoO4-AgBr composite compared to pure AgBr and Ag2MoO4 crystals (37.6% and 348.4% enhancement respectively). The Ag@Ag2MoO4-AgBr composite cloud degraded Rhodamin B, bromophenol blue, and amino black 10b completed in 7min.

  10. Microwave-enhanced synthesis of magnetic porous covalent triazine-based framework composites for fast separation of organic dye from aqueous solution.

    PubMed

    Zhang, Wang; Liang, Fei; Li, Cun; Qiu, Ling-Guang; Yuan, Yu-Peng; Peng, Fu-Min; Jiang, Xia; Xie, An-Jian; Shen, Yu-Hua; Zhu, Jun-Fa

    2011-02-28

    A novel type of magnetic porous carbonaceous polymeric material, CTF/Fe(2)O(3) composite (CTF = covalent triazine-based framework), has been synthesized by a facile microwave-enhanced high-temperature ionothermal method. By selecting ZnCl(2) as a reaction medium and the Lewis acid catalyst, and choosing FeCl(3)·6H(2)O as an iron oxide precursor, a series of CTF/Fe(2)O(3) composites with different γ-Fe(2)O(3) contents has been prepared in 60 min. The resulting samples were characterized by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and N(2) sorption-desorption isotherms. The obtained CTF/Fe(2)O(3) composites exhibit high surface areas (930-1149 m(2) g(-1)), and their saturation magnetizations at 300 K vary from 1.1 to 5.9 emu g(-1), depending respectively on different Fe(2)O(3) contents (6.43-12.43 wt%) in the CTF/Fe(2)O(3) composites. The CTF/Fe(2)O(3) composites were applied to remove organic dye from aqueous solution by selecting methyl orange as a model molecule, and both high adsorption capacity (291 mg g(-1), corresponding to 0.889 mmol g(-1)) and fast adsorption kinetics (k(ads) = 4.31 m(2) mg(-1) min(-1)) were observed.

  11. Platinum-Free Counter Electrode Comprised of Metal-Organic-Framework (MOF)-Derived Cobalt Sulfide Nanoparticles for Efficient Dye-Sensitized Solar Cells (DSSCs)

    PubMed Central

    Hsu, Shao-Hui; Li, Chun-Ting; Chien, Heng-Ta; Salunkhe, Rahul R.; Suzuki, Norihiro; Yamauchi, Yusuke; Ho, Kuo-Chuan; Wu, Kevin C.-W.

    2014-01-01

    We fabricated a highly efficient (with a solar-to-electricity conversion efficiency (η) of 8.1%) Pt-free dye-sensitized solar cell (DSSC). The counter electrode was made of cobalt sulfide (CoS) nanoparticles synthesized via surfactant-assisted preparation of a metal organic framework, ZIF-67, with controllable particle sizes (50 to 320 nm) and subsequent oxidation and sulfide conversion. In contrast to conventional Pt counter electrodes, the synthesized CoS nanoparticles exhibited higher external surface areas and roughness factors, as evidenced by X-ray diffraction (XRD), scanning electron microscopy (SEM) element mapping, and electrochemical analysis. Incident photon-to-current conversion efficiency (IPCE) results showed an increase in the open circuit voltage (VOC) and a decrease in the short-circuit photocurrent density (Jsc) for CoS-based DSSCs compared to Pt-based DSSCs, resulting in a similar power conversion efficiency. The CoS-based DSSC fabricated in the study show great potential for economically friendly production of Pt-free DSSCs. PMID:25382139

  12. Photoinduced electron transfer (PET) versus excimer formation in supramolecular p/n-heterojunctions of perylene bisimide dyes and implications for organic photovoltaics.

    PubMed

    Nowak-Król, Agnieszka; Fimmel, Benjamin; Son, Minjung; Kim, Dongho; Würthner, Frank

    2015-01-01

    Foldamer systems comprised of two perylene bisimide (PBI) dyes attached to the conjugated backbones of 1,2-bis(phenylethynyl)benzene and phenylethynyl-bis(phenylene)indane, respectively, were synthesized and investigated with regard to their solvent-dependent properties. UV/Vis absorption and steady-state fluorescence spectra show that both foldamers exist predominantly in a folded H-aggregated state consisting of π-π-stacked PBIs in THF and in more random conformations with weaker excitonic coupling between the PBIs in chloroform. Time-resolved fluorescence spectroscopy and transient absorption spectroscopy reveal entirely different relaxation pathways for the photoexcited molecules in the given solvents, i.e. photoinduced electron transfer leading to charge separated states for the open conformations (in chloroform) and relaxation into excimer states with red-shifted emission for the stacked conformations (in THF). Supported by redox data from cyclic voltammetry and Rehm-Weller analysis we could relate the processes occurring in these solution-phase model systems to the elementary processes in organic solar cells. Accordingly, only if relaxation pathways such as excimer formation are strictly avoided in molecular semiconductor materials, excitons may diffuse over larger distances to the heterojunction interface and produce photocurrent via the formation of electron/hole pairs by photoinduced electron transfer.

  13. High-efficiency sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays.

    PubMed

    Guo, Xiao; Fu, Yongming; Hong, Deyi; Yu, Binwei; He, Haoxuan; Wang, Qiang; Xing, Lili; Xue, Xinyu

    2016-09-16

    Highly-efficient sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays was achieved. A steel screen was used as the substrate for supporting FeS/ZnO nanoarrays, and the nanoarrays were vertically and uniformly grown on the substrate via a wet-chemical route. Under ultrasonic and solar irradiation, FeS/ZnO nanoarrays have high sono-photocatalytic activity for degrading methylene blue in water. The photogenerated carriers can be separated by a piezoelectric field and a built-in electric field, resulting in a low recombination rate and high photocatalytic efficiency. The piezophototronic and photocatalytic effects were coupled together. The experimental/theoretical data indicate that this novel wastewater treatment can co-use mechanical and solar energy in nature, and so is a promising technology for environment improvement.

  14. High-efficiency sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays.

    PubMed

    Guo, Xiao; Fu, Yongming; Hong, Deyi; Yu, Binwei; He, Haoxuan; Wang, Qiang; Xing, Lili; Xue, Xinyu

    2016-09-16

    Highly-efficient sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays was achieved. A steel screen was used as the substrate for supporting FeS/ZnO nanoarrays, and the nanoarrays were vertically and uniformly grown on the substrate via a wet-chemical route. Under ultrasonic and solar irradiation, FeS/ZnO nanoarrays have high sono-photocatalytic activity for degrading methylene blue in water. The photogenerated carriers can be separated by a piezoelectric field and a built-in electric field, resulting in a low recombination rate and high photocatalytic efficiency. The piezophototronic and photocatalytic effects were coupled together. The experimental/theoretical data indicate that this novel wastewater treatment can co-use mechanical and solar energy in nature, and so is a promising technology for environment improvement. PMID:27502445

  15. The Enhanced Catalytic Activities of Asymmetric Au-Ni Nanoparticle Decorated Halloysite-Based Nanocomposite for the Degradation of Organic Dyes

    NASA Astrophysics Data System (ADS)

    Jia, Lei; Zhou, Tao; Xu, Jun; Li, Xiaohui; Dong, Kun; Huang, Jiancui; Xu, Zhouqing

    2016-02-01

    Janus particles (JPs) are unique among the nano-/microobjects because they provide asymmetry and can thus impart drastically different chemical or physical properties. In this work, we have fabricated the magnetic halloysite nanotube (HNT)-based HNTs@Fe3O4 nanocomposite (NCs) and then anchored the Janus Au-Ni or isotropic Au nanoparticles (NPs) to the surface of external wall of sulfydryl modified magnetic nanotubes. The characterization by physical methods authenticates the successful fabrication of two different magnetic HNTs@Fe3O4@Au and HNTs@Fe3O4@Au-Ni NCs. The catalytic activity and recyclability of the two NCs have been evaluated considering the degradation of Congo red (CR) and 4-nitrophenol (4-NP) using sodium borohydride as a model reaction. The results reveal that the symmetric Au NPs participated NCs display low activity in the degradation of the above organic dyes. However, a detailed kinetic study demonstrates that the employ of bimetallic Janus Au-Ni NPs in the NCs indicates enhanced catalytic activity, owing to the structurally specific nature. Furthermore, the magnetic functional NCs reported here can be used as recyclable catalyst which can be recovered simply by magnet.

  16. Characterization of anthocyanin based dye-sensitized organic solar cells (DSSC) and modifications based on bio-inspired ion mobility improvements

    NASA Astrophysics Data System (ADS)

    Mawyin, Jose Amador

    The worldwide electrical energy consumption will increase from currently 10 terawatts to 30 terawatts by 2050. To decrease the current atmospheric CO2 would require our civilization to develop a 20 terawatts non-greenhouse emitting (renewable) electrical power generation capability. Solar photovoltaic electric power generation is thought to be a major component of proposed renewable energy-based economy. One approach to less costly, easily manufactured solar cells is the Dye-sensitized solar cells (DSSC) introduced by Greatzel and others. This dissertation describes the work focused on improving the performance of DSSC type solar cells. In particular parameters affecting dye-sensitized solar cells (DSSC) based on anthocyanin pigments extracted from California blackberries (Rubus ursinus) and bio-inspired modifications were analyzed and solar cell designs optimized. Using off-the-shelf materials DSSC were constructed and tested using a custom made solar spectrum simulator and photoelectric property characterization. This equipment facilitated the taking of automated I-V curve plots and the experimental determination of parameters such as open circuit voltage (V OC), short circuit current (JSC), fill factor (FF), etc. This equipment was used to probe the effect of various modifications such as changes in the annealing time and composition of the of the electrode counter-electrode. Solar cell optimization schemes included novel schemes such as solar spectrum manipulation to increase the percentage of the solar spectrum capable of generating power in the DSSC. Solar manipulation included light scattering and photon upconversion. Techniques examined here focused on affordable materials such as silica nanoparticles embedded inside a TiO2 matrix. Such materials were examined for controlled scattering of visible light and optimize light trapping within the matrix as well as a means to achieve photon up-energy-conversion using the Raman effect in silica nano-particles (due

  17. Facile one-pot synthesis of organic dye-complexed microgels for optical detection of glucose at physiological pH.

    PubMed

    Li, Yingyu; Zhou, Shuiqin

    2013-06-21

    With a rational design of functional co-monomers, low-cost dye-complexed microgels, capable of continuous glucose detection at physiological pH, were readily synthesized in one-pot via precipitation polymerization in water.

  18. Synergistic inhibition behavior between indigo carmine and cetyl trimethyl ammonium bromide on carbon steel corroded in a 0.5 M HCl solution

    NASA Astrophysics Data System (ADS)

    Zhang, Zhe; Tian, Ningchen; Li, Xiuying; Zhang, Lingzhi; Wu, Ling; Huang, Yan

    2015-12-01

    This work reports on a newly observed synergistic inhibition between indigo carmine and cetyl trimethyl ammonium bromide (CTAB) on 1045 carbon steel (CS) corroded in a 0.5 M HCl solution. The results of electrochemical measurements showed that CTAB could change indigo carmine in a manner that would accelerate corrosion and produce an effective inhibitor. The maximal protection efficiency was significantly greater than 0.985, with the concentration of the combination inhibitors reaching approximately 5 × 10-5 M. The microstructure of the CS corrosion surface demonstrated that the indigo disulfonate anions and cetyltrimethylammonium cations were adsorbed simultaneously on the CS surface to protect it from corrosion. Diffusion coefficient analysis and the surface concentration profiles of the corrosive species were used to investigate the synergistic effect of the indigo carmine/CTAB combination inhibitors, and the results demonstrate the existence of synergy.

  19. Dark dyes-bright complexes: fluorogenic protein labeling.

    PubMed

    Bruchez, Marcel P

    2015-08-01

    Complexes formed between organic dyes and genetically encoded proteins combine the advantages of stable and tunable fluorescent molecules and targetable, biologically integrated labels. To overcome the challenges imposed by labeling with bright fluorescent dyes, a number of approaches now exploit chemical or environmental changes to control the properties of a bound dye, converting dyes from a weakly fluorescent state to a bright, easily detectable complex. Optimized, such approaches avoid the need for removal of unbound dyes, facilitate rapid and simple assays in cultured cells and enable hybrid labeling to function more robustly in living model organisms.

  20. Pickering emulsions prepared by layered niobate K₄Nb₆O₁₇ intercalated with organic cations and photocatalytic dye decomposition in the emulsions.

    PubMed

    Nakato, Teruyuki; Ueda, Hiroaki; Hashimoto, Sachika; Terao, Ryosuke; Kameyama, Miyuki; Mouri, Emiko

    2012-08-01

    We investigated emulsions stabilized with particles of layered hexaniobate, known as a semiconductor photocatalyst, and photocatalytic degradation of dyes in the emulsions. Hydrophobicity of the niobate particles was adjusted with the intercalation of alkylammonium ions into the interlayer spaces to enable emulsification in a toluene-water system. After the modification of interlayer space with hexylammonium ions, the niobate stabilized water-in-oil (w/o) emulsions in a broad composition range. Optical microscopy showed that the niobate particles covered the surfaces of emulsion droplets and played a role of emulsifying agents. The niobate particles also enabled the generation of oil-in-water (o/w) emulsions in a limited composition range. Modification with dodecylammonium ions, which turned the niobate particles more hydrophobic, only gave w/o emulsions, and the particles were located not only at the toluene-water interface but also inside the toluene continuous phase. On the other hand, interlayer modification with butylammonium ions led to the formation of o/w emulsions. When porphyrin dyes were added to the system, the cationic dye was adsorbed on niobate particles at the emulsion droplets whereas the lipophilic dye was dissolved in toluene. Upon UV irradiation, both of the dyes were degraded photocatalytically. When the cationic and lipophilic porphyrin molecules were simultaneously added to the emulsions, both of the dyes were photodecomposed nonselectively.

  1. Application of surface-enhanced Raman scattering (SERS) for the identification of anthraquinone dyes used in works of art

    NASA Astrophysics Data System (ADS)

    Chen, K.; Leona, Marco; Vo-Dinh, K. C.; Yan, F.; Wabuyele, M.; Vo-Dinh, Tuan

    2005-11-01

    Surface-enhanced Raman scattering (SERS) was investigated for applications in the analysis of anthraquinone dyes used in works of art. Two SERS procedures were developed and evaluated with frequently used anthraquinone dyes, alizarin, carminic acid and lac dye. The first procedure involves the removal of a microscopic fragment containing alizarin from a painting, and a layer of silver nanoparticles was thermally evaporated directly on the fragment to induce SERS signal from alizarin. The applicability of this procedure for analyzing solid samples of color layer from paintings was discussed in detail. In the second procedure, a SERS-active substrate was prepared by spin-coating an alumina-nanoparticle layer onto a glass slide, followed by thermally evaporating a layer of silver nanoparticles on top of the alumina layer. Aliquots of dye solutions were delivered onto this substrate where intense SERS spectra characteristic of alizarin, carminic acid, and lac dye were obtained. The effects of two parameters, the concentration of the alumina suspension, and the thickness of the silver nanoparticle layer, on the performance of the Ag-Al2O3 substrate were examined with alizarin as the model compound. Comparative studies with other common SERS substrates showed larger enhancement and improved reproducibility for the Ag-Al2O3 substrate. The potential applicability of the Ag-Al2O3 substrate for the analysis of real artifact objects was illustrated by the identification of alizarin extracted from a small piece of textile dyed with traditional methods and materials. The limit of detection for alizarin was estimated to be 7×10-15 g from tests using solutions of known concentration.

  2. Textile dye dermatitis.

    PubMed

    Hatch, K L; Maibach, H I

    1995-04-01

    The literature concerning textile dye dermatitis published during the last decade was reviewed. Sixty-one cases of dye-allergic contact dermatitis in which the presentation or course of the dermatitis was unusual or the dye allergen was one not previously reported have been described. The four new dye allergens discovered were Disperse Blue 106, Disperse Blue 85, Disperse Brown 1, and Basic Red 46. The incidence of dye dermatitis varied from 1% to 15.9% depending on the country, patient sample, and number of dyes in the patch test series. The 10 new dye allergens discovered in these studies were Disperse Blue 153, Disperse Orange 13, Basic Black 1, Basic Brown 1, the acid dyes Supramine Yellow and Supramine Red, the direct dye Diazol Orange, the basic dye Brilliant Green, Turquoise Reactive, and Neutrichrome Red. Disperse Blue 106 and Disperse Blue 124 were shown to be the strongest clothing dye sensitizers to date. Standard screening patch test series were found to be inadequate for the detection of textile dye sensitivity; therefore textile dye patch test series should be used. It is difficult to determine whether the incidence of dye dermatitis is increasing or decreasing because controlled epidemiologic studies are lacking, but data suggest that textile dye sensitivity is more common than previously believed.

  3. Synthesis, Photophysics, Electrochemistry and Electrogenerated Chemiluminescence of PEG-Modified BODIPY dyes in Organic and Aqueous Solutions

    PubMed Central

    Nepomnyashchii, Alexander B.; Pistner, Allen J.; Bard, Allen J.; Rosenthal, Joel

    2013-01-01

    A set polyethylene glycol (PEG) appended BODIPY architectures (BOPEG1 – BOPEG3) have been prepared and studied in CH2Cl2, H2O:CH3CN (1:1) and aqueous solutions. BOPEG1 and BOPEG2 both contain a short PEG chain and differ in substitution about the BODIPY framework. BOPEG3 is comprised of a fully substituted BODIPY moiety linked to a PEG polymer that is roughly 13 units in length. The photophysics and electrochemical properties of these compounds have been thoroughly characterized in CH2Cl2 and aqueous CH3CN solutions. The behavior of BOPEG1 – BOPEG3 correlates with established rules of BODIPY stability based on substitution about the BODIPY moiety. ECL for each of these compounds was also monitored. BOPEG1, which is unsubstituted at the 2- and 6-positions dimerized upon electrochemical oxidation while BOPEG2, which contains ethyl groups at the 2- and 6-positions, was much more robust and served as an excellent ECL luminophore. BOPEG3 is highly soluble in water due to the long PEG tether and demonstrated modest ECL activity in aqueous solutions using tri-n-propylamine (TPrA) as a coreactant. As such, BOPEG3 represents the first BODIPY derivative that has been shown to display ECL in water without the need for an organic cosolvent, and marks an important step in the development of BODIPY based ECL probes for various biosensing applications. PMID:23626863

  4. Supersensitization of CdS quantum dots with a near-infrared organic dye: toward the design of panchromatic hybrid-sensitized solar cells.

    PubMed

    Choi, Hyunbong; Nicolaescu, Roxana; Paek, Sanghyun; Ko, Jaejung; Kamat, Prashant V

    2011-11-22

    The photoresponse of quantum dot solar cells (QDSCs) has been successfully extended to the near-IR (NIR) region by sensitizing nanostructured TiO(2)-CdS films with a squaraine dye (JK-216). CdS nanoparticles anchored on mesoscopic TiO(2) films obtained by successive ionic layer adsorption and reaction (SILAR) exhibit limited absorption below 500 nm with a net power conversion efficiency of ~1% when employed as a photoanode in QDSC. By depositing a thin barrier layer of Al(2)O(3), the TiO(2)-CdS films were further modified with a NIR absorbing squaraine dye. Quantum dot sensitized solar cells supersensitized with a squariand dye (JK-216) showed good stability during illumination with standard global AM 1.5 solar conditions, delivering a maximum overall power conversion efficiency (η) of 3.14%. Transient absorption and pulse radiolysis measurements provide further insight into the excited state interactions of squaraine dye with SiO(2), TiO(2), and TiO(2)/CdS/Al(2)O(3) films and interfacial electron transfer processes. The synergy of combining semiconductor quantum dots and NIR absorbing dye provides new opportunities to harvest photons from different regions of the solar spectrum.

  5. Interaction of Sensitizing Dyes with Nanostructured TiO2 Film in Dye-Sensitized Solar Cells Using Terahertz Spectroscopy

    PubMed Central

    Ghann, William; Rahman, Aunik; Rahman, Anis; Uddin, Jamal

    2016-01-01

    The objective of this investigation was to shed light on the nature of interaction of different organic dyes and an inorganic dye, Ruthenium (II) polypyridine complex, with TiO2 nanoparticles. TiO2 is commonly deployed as an efficient energy transfer electrode in dye sensitized solar cells. The efficiency of dye sensitized solar cells is a function of the interaction of a dye with the electrode material such as TiO2. To the best of our knowledge the present study is the first effort in the determination of terahertz absorbance signals, investigation of real-time dye permeation kinetics, and the surface profiling and 3D imaging of dye sensitized TiO2 films. Herein, we report that the terahertz spectra of the natural dye sensitized TiO2 films were distinctively different from that of the inorganic dye with prominent absorption of natural dyes occurring at approximately the same wavelength. It was observed that the permeation of the natural dyes were more uniform through the layers of the mesoporous TiO2 compared to the inorganic dye. Finally, defects and flaws on TiO2 film were easily recognized via surface profiling and 3D imaging of the films. The findings thus offer a new approach in characterization of dye sensitized solar cells. PMID:27443236

  6. Interaction of Sensitizing Dyes with Nanostructured TiO2 Film in Dye-Sensitized Solar Cells Using Terahertz Spectroscopy.

    PubMed

    Ghann, William; Rahman, Aunik; Rahman, Anis; Uddin, Jamal

    2016-07-22

    The objective of this investigation was to shed light on the nature of interaction of different organic dyes and an inorganic dye, Ruthenium (II) polypyridine complex, with TiO2 nanoparticles. TiO2 is commonly deployed as an efficient energy transfer electrode in dye sensitized solar cells. The efficiency of dye sensitized solar cells is a function of the interaction of a dye with the electrode material such as TiO2. To the best of our knowledge the present study is the first effort in the determination of terahertz absorbance signals, investigation of real-time dye permeation kinetics, and the surface profiling and 3D imaging of dye sensitized TiO2 films. Herein, we report that the terahertz spectra of the natural dye sensitized TiO2 films were distinctively different from that of the inorganic dye with prominent absorption of natural dyes occurring at approximately the same wavelength. It was observed that the permeation of the natural dyes were more uniform through the layers of the mesoporous TiO2 compared to the inorganic dye. Finally, defects and flaws on TiO2 film were easily recognized via surface profiling and 3D imaging of the films. The findings thus offer a new approach in characterization of dye sensitized solar cells.

  7. Interaction of Sensitizing Dyes with Nanostructured TiO2 Film in Dye-Sensitized Solar Cells Using Terahertz Spectroscopy

    NASA Astrophysics Data System (ADS)

    Ghann, William; Rahman, Aunik; Rahman, Anis; Uddin, Jamal

    2016-07-01

    The objective of this investigation was to shed light on the nature of interaction of different organic dyes and an inorganic dye, Ruthenium (II) polypyridine complex, with TiO2 nanoparticles. TiO2 is commonly deployed as an efficient energy transfer electrode in dye sensitized solar cells. The efficiency of dye sensitized solar cells is a function of the interaction of a dye with the electrode material such as TiO2. To the best of our knowledge the present study is the first effort in the determination of terahertz absorbance signals, investigation of real-time dye permeation kinetics, and the surface profiling and 3D imaging of dye sensitized TiO2 films. Herein, we report that the terahertz spectra of the natural dye sensitized TiO2 films were distinctively different from that of the inorganic dye with prominent absorption of natural dyes occurring at approximately the same wavelength. It was observed that the permeation of the natural dyes were more uniform through the layers of the mesoporous TiO2 compared to the inorganic dye. Finally, defects and flaws on TiO2 film were easily recognized via surface profiling and 3D imaging of the films. The findings thus offer a new approach in characterization of dye sensitized solar cells.

  8. Interaction of Sensitizing Dyes with Nanostructured TiO2 Film in Dye-Sensitized Solar Cells Using Terahertz Spectroscopy.

    PubMed

    Ghann, William; Rahman, Aunik; Rahman, Anis; Uddin, Jamal

    2016-01-01

    The objective of this investigation was to shed light on the nature of interaction of different organic dyes and an inorganic dye, Ruthenium (II) polypyridine complex, with TiO2 nanoparticles. TiO2 is commonly deployed as an efficient energy transfer electrode in dye sensitized solar cells. The efficiency of dye sensitized solar cells is a function of the interaction of a dye with the electrode material such as TiO2. To the best of our knowledge the present study is the first effort in the determination of terahertz absorbance signals, investigation of real-time dye permeation kinetics, and the surface profiling and 3D imaging of dye sensitized TiO2 films. Herein, we report that the terahertz spectra of the natural dye sensitized TiO2 films were distinctively different from that of the inorganic dye with prominent absorption of natural dyes occurring at approximately the same wavelength. It was observed that the permeation of the natural dyes were more uniform through the layers of the mesoporous TiO2 compared to the inorganic dye. Finally, defects and flaws on TiO2 film were easily recognized via surface profiling and 3D imaging of the films. The findings thus offer a new approach in characterization of dye sensitized solar cells. PMID:27443236

  9. Anthracene/phenothiazine π-conjugated sensitizers for dye-sensitized solar cells using redox mediator in organic and water-based solvents.

    PubMed

    Lin, Ryan Yeh-Yung; Chuang, Tzu-Man; Wu, Feng-Ling; Chen, Pei-Yu; Chu, Te-Chun; Ni, Jen-Shyang; Fan, Miao-Syuan; Lo, Yih-Hsing; Ho, Kuo-Chuan; Lin, Jiann T

    2015-01-01

    Metal-free dyes (MD1 to MD5) containing an anthracene/phenothiazine unit in the spacer have been synthesized. The conversion efficiency (7.13 %) of the dye-sensitized solar cell using MD3 as the sensitizer reached approximately 85 % of the N719-based standard cell (8.47 %). The cell efficiency (8.42 %) of MD3-based dye-sensitized solar cells (DSSCs) with addition of chenodeoxycholic acid is comparable with that of N719-based standard cell. The MD3 water-based DSSCs using a dual-TEMPO (2,2,6,6-tetramethylpiperidine-N-oxyl)/iodide electrolyte exhibited very promising cell performance of 4.96 % with an excellent Voc of 0.77 V.

  10. Anthraquinone dyes decolorization capacity of anamorphic Bjerkandera adusta CCBAS 930 strain and its HRP-like negative mutants.

    PubMed

    Korniłłowicz-Kowalska, Teresa; Rybczyńska, Kamila

    2014-06-01

    Cultures of the anamorphic fungus Bjerkandera adusta CCBAS 930 decolorizing, in stationary cultures, 0.01 % solutions of carminic acid and Poly R-478, were characterised by a strong increase in the activity of the horseradish peroxidase (HRP-like) and manganese-dependent peroxidase (MnP) at a low activity of lignin peroxidase. Genotypically modified mutants of B. adusta CCBAS 930: 930-5 and 930-14, with total or partial loss of decolorization capabilities relative to anthraquinonic dyes, showed inhibition of the activity of HRP-like peroxidase and MnP. Whereas, compared to the parental strain, in the mutant cultures there was an increase in the activity of lignin peroxidase and laccase. The paper presents a discussion of the role of the studied enzymatic activities in the process of decolorization of anthraquinonic dyes by the strain B. adusta CCBAS 930. PMID:24415463

  11. Identification of anthraquinone coloring matters in natural red dyes by electrospray mass spectrometry coupled to capillary electrophoresis.

    PubMed

    Puchalska, Maria; Orlińska, Magdalena; Ackacha, Mohamed A; Połeć-Pawlak, Kasia; Jarosz, Maciej

    2003-12-01

    Capillary electrophoresis with UV/visible diode-array detection (DAD) and electrospray mass spectrometric (ESI-MS) detection were used for the identification of anthraquinone color components of cochineal, lac-dye and madder, natural red dyestuffs often used by ancient painters. For the purpose of such analysis, ESI-MS was found to be a much more appropriate detection technique than DAD one owing to its higher sensitivity (detection limits in the range 0.1-0.5 micro g ml(-1)) and selectivity. The method developed made it possible to identify unequivocally carminic acid and laccaic acids A, B and E as coloring matters in the examined preparations of cochineal and lac-dye, respectively. In madder, European Rubia tinctorum, alizarin and purpurin were found. The method allows the rapid, direct and straightforward identification and quantification of components of natural products used in art and could be very helpful in restoration and conservation procedures. PMID:14696204

  12. Cloth dye poisoning

    MedlinePlus

    ... poisonous ingredient in most household cloth dyes. Most common household cloth dyes are made from nonpoisonous substances, such as: Mild soaps Pigments Salts Although these substances are generally considered not dangerous, ...

  13. Evaluation of potential genotoxicity of five food dyes using the somatic mutation and recombination test.

    PubMed

    Sarıkaya, Rabia; Selvi, Mahmut; Erkoç, Figen

    2012-08-01

    In this study, different concentrations of five food dyes (amaranth, patent blue, carminic acid, indigotine and erythrosine) have been evaluated for genotoxicity in the Somatic Mutation and Recombination Test (SMART) of Drosophila melanogaster. Standard cross was used in the experiment. Larvae including two linked recessive wing hair mutations were chronically fed at different concentrations of the test compounds in standard Drosophila Instant Medium. Feeding ended with pupation of the surviving larvae. Wings of the emerging adult flies were scored for the presence of spots of mutant cells which can result from either somatic mutation or somatic recombination. For the evaluation of genotoxic effects, the frequencies of spots per wing in the treated series were compared to the control group, which was distilled water. The present study shows that carminic acid and indigotine demonstrated negative results while erythrosine demonstrated inconclusive results. In addition 25 mg mL(-1) concentration of patent blue and 12.5, 25 and 50 mg mL(-1) concentrations of amaranth demonstrated positive results in the SMART.

  14. Evaluation of potential genotoxicity of five food dyes using the somatic mutation and recombination test.

    PubMed

    Sarıkaya, Rabia; Selvi, Mahmut; Erkoç, Figen

    2012-08-01

    In this study, different concentrations of five food dyes (amaranth, patent blue, carminic acid, indigotine and erythrosine) have been evaluated for genotoxicity in the Somatic Mutation and Recombination Test (SMART) of Drosophila melanogaster. Standard cross was used in the experiment. Larvae including two linked recessive wing hair mutations were chronically fed at different concentrations of the test compounds in standard Drosophila Instant Medium. Feeding ended with pupation of the surviving larvae. Wings of the emerging adult flies were scored for the presence of spots of mutant cells which can result from either somatic mutation or somatic recombination. For the evaluation of genotoxic effects, the frequencies of spots per wing in the treated series were compared to the control group, which was distilled water. The present study shows that carminic acid and indigotine demonstrated negative results while erythrosine demonstrated inconclusive results. In addition 25 mg mL(-1) concentration of patent blue and 12.5, 25 and 50 mg mL(-1) concentrations of amaranth demonstrated positive results in the SMART. PMID:22482698

  15. Method of dye removal for the textile industry

    SciTech Connect

    Stone, M.L.

    2000-07-25

    The invention comprises a method of processing a waste stream containing dyes, such as a dye bath used in the textile industry. The invention uses an inorganic-based polymer, such as polyphosphazene, to separate dyes and/or other chemicals from the waste stream. Membranes comprising polyphosphazene have the chemical and thermal stability to survive the harsh, high temperature environment of dye waste streams, and have been shown to completely separate dyes from the waste stream. Several polyphosplhazene membranes having a variety of organic substituent have been shown effective in removing color from waste streams.

  16. Method of dye removal for the textile industry

    DOEpatents

    Stone, Mark L.

    2000-01-01

    The invention comprises a method of processing a waste stream containing dyes, such as a dye bath used in the textile industry. The invention comprises using an inorganic-based polymer, such as polyphosphazene, to separate dyes and/or other chemicals from the waste stream. Membranes comprising polyphosphazene have the chemical and thermal stability to survive the harsh, high temperature environment of dye waste streams, and have been shown to completely separate dyes from the waste stream. Several polyphosplhazene membranes having a variety of organic substituent have been shown effective in removing color from waste streams.

  17. The Development and Application of Novel IR and NMR-Based Model for the Evaluation of Carminative Effect of Artemisia judaica L. Essential Oil

    PubMed Central

    Alzweiri, Muhammed; Alrawashdeh, Ibrahim M.; Bardaweel, Sanaa K.

    2014-01-01

    Artemisia judaica L. is a medicinal plant that is traditionally used to relieve abdominal pains through its carminative activity. In this study, spectroscopic analysis was employed to investigate the carminative activity associated with A. judaica. Using infrared spectroscopy, the carminative activity was evaluated based on the first derivative of IR-characteristic stretching signal of CO2. Our results indicate that A. judaica oil effectively reduced the response of CO2 signal equivalent to thymol standard. Additionally, 1H-NMR spectroscopy was utilized to assess surface activity of A. judaica crude oil through the reduction of interfacial tension in a D2O/CDCl3 system. Apparently, 10 mg of the oil was able to solubilize water in a chloroform layer up to 4.3% (w/w). In order to correlate the observed surface activity of the oil to its actual composition, GC-MS and GC-FID structural analysis were undertaken. The results revealed that the oil composition consists of oxygenated terpenes which might be responsible for the carminative effect. Furthermore, owing to its sensitivity, our model provides a fundamental basis for the pharmacological assessment of trace amounts of oils with high precision and accuracy. PMID:25614741

  18. Sonochemical assisted hydrothermal synthesis of ZnO: Cr nanoparticles loaded activated carbon for simultaneous ultrasound-assisted adsorption of ternary toxic organic dye: Derivative spectrophotometric, optimization, kinetic and isotherm study.

    PubMed

    Jamshidi, M; Ghaedi, M; Dashtian, K; Hajati, S; Bazrafshan, A A

    2016-09-01

    Chromium doped zinc oxide nanoparticles (ZnO: Cr-NPs) was synthesized by ultrasonically assisted hydrothermal method and characterized by FE-SEM, XRD and TEM analysis. Subsequently, this composite ultrasonically assisted was deposited on activated carbon (ZnO: Cr-NPs-AC) and used for simultaneous ultrasound-assisted removal of three toxic organic dye namely of malachite green (MG), eosin yellow (EY) and Auramine O (AO). Dyes spectra overlap in mixture (major problem for simultaneous investigation) of this systems was extensively resolved by derivative spectrophotometric method. The magnitude of variables like initial dyes concentration, adsorbent mass and sonication time influence on dyes removal was optimized using small central composite design (CCD) combined with desirability function (DF) approach, while pH was studied by one-a-time approach. The maximized removal percentages at desirability of 0.9740 was set as follow: pH 6.0, 0.019g ZnO: Cr-NPs-AC, 3.9min sonication at 4.5, 4.8 and 4.7mgL(-1) of MG, EY and AO, respectively. Above optimized points lead to achievement of removal percentage of 98.36%, 97.24%, and 99.26% correspond to MG, EY and AO, respectively. ANOVA for each dyes based p-value less than (<0.0001) suggest highly efficiency of CCD model for prediction of data concern to simultaneous removal of these dyes within 95% confidence interval, while their F-value for MG, EY and AO is 935, 800.2, and 551.3, respectively, that confirm low participation of this them in signal. The value of multiple correlation coefficient R(2), adjusted and predicted R(2) for simultaneous removal of MG is 0.9982, 0.9972 and 0.9940, EY is 0.9979, 0.9967 and 0.9930 and for AO is 0.9970, 0.9952 and 0.9939. The adsorption rate well fitted by pseudo second-order and Langmuir model via high, economic and profitable adsorption capacity of 214.0, 189.7 and 211.6mgg(-1) for MG, EY and AO, respectively. PMID:27150752

  19. Sonochemical assisted hydrothermal synthesis of ZnO: Cr nanoparticles loaded activated carbon for simultaneous ultrasound-assisted adsorption of ternary toxic organic dye: Derivative spectrophotometric, optimization, kinetic and isotherm study.

    PubMed

    Jamshidi, M; Ghaedi, M; Dashtian, K; Hajati, S; Bazrafshan, A A

    2016-09-01

    Chromium doped zinc oxide nanoparticles (ZnO: Cr-NPs) was synthesized by ultrasonically assisted hydrothermal method and characterized by FE-SEM, XRD and TEM analysis. Subsequently, this composite ultrasonically assisted was deposited on activated carbon (ZnO: Cr-NPs-AC) and used for simultaneous ultrasound-assisted removal of three toxic organic dye namely of malachite green (MG), eosin yellow (EY) and Auramine O (AO). Dyes spectra overlap in mixture (major problem for simultaneous investigation) of this systems was extensively resolved by derivative spectrophotometric method. The magnitude of variables like initial dyes concentration, adsorbent mass and sonication time influence on dyes removal was optimized using small central composite design (CCD) combined with desirability function (DF) approach, while pH was studied by one-a-time approach. The maximized removal percentages at desirability of 0.9740 was set as follow: pH 6.0, 0.019g ZnO: Cr-NPs-AC, 3.9min sonication at 4.5, 4.8 and 4.7mgL(-1) of MG, EY and AO, respectively. Above optimized points lead to achievement of removal percentage of 98.36%, 97.24%, and 99.26% correspond to MG, EY and AO, respectively. ANOVA for each dyes based p-value less than (<0.0001) suggest highly efficiency of CCD model for prediction of data concern to simultaneous removal of these dyes within 95% confidence interval, while their F-value for MG, EY and AO is 935, 800.2, and 551.3, respectively, that confirm low participation of this them in signal. The value of multiple correlation coefficient R(2), adjusted and predicted R(2) for simultaneous removal of MG is 0.9982, 0.9972 and 0.9940, EY is 0.9979, 0.9967 and 0.9930 and for AO is 0.9970, 0.9952 and 0.9939. The adsorption rate well fitted by pseudo second-order and Langmuir model via high, economic and profitable adsorption capacity of 214.0, 189.7 and 211.6mgg(-1) for MG, EY and AO, respectively.

  20. Seeking effective dyes for a mediated glucose-air alkaline battery/fuel cell

    NASA Astrophysics Data System (ADS)

    Eustis, Ross; Tsang, Tsz Ming; Yang, Brigham; Scott, Daniel; Liaw, Bor Yann

    2014-02-01

    A significant level of power generation from an abiotic, air breathing, mediated reducing sugar-air alkaline battery/fuel cell has been achieved in our laboratories at room temperature without complicated catalysis or membrane separation in the reaction chamber. Our prior studies suggested that mass transport limitation by the mediator is a limiting factor in power generation. New and effective mediators were sought here to improve charge transfer and power density. Forty-five redox dyes were studied to identify if any can facilitate mass transport in alkaline electrolyte solution; namely, by increasing the solubility and mobility of the dye, and the valence charge carried per molecule. Indigo dyes were studied more closely to understand the complexity involved in mass transport. The viability of water-miscible co-solvents was also explored to understand their effect on solubility and mass transport of the dyes. Using a 2.0 mL solution, 20% methanol by volume, with 100 mM indigo carmine, 1.0 M glucose and 2.5 M sodium hydroxide, the glucose-air alkaline battery/fuel cell attained 8 mA cm-2 at short-circuit and 800 μW cm-2 at the maximum power point. This work shall aid future optimization of mediated charge transfer mechanism in batteries or fuel cells.

  1. Simple method for the analysis of food dyes on reversed-phase thin-layer plates.

    PubMed

    Oka, H; Ikai, Y; Kawamura, N; Yamada, M; Inoue, H; Ohno, T; Inagaki, K; Kuno, A; Yamamoto, N

    1987-12-18

    A technique for the determination of food dyes using reversed-phase thin-layer chromatography on octadecyl-modified silica is described. A solvent system containing 5.0% aqueous sodium sulphate solution enables good separation of the food dyes. Their separation is dependent on the pH of the solvent system, good separation among all dyes being obtained between pH 6.0 and 7.0. The determination of thirteen dyes can be achieved by a combination of methanol-acetonitrile-5.0% aqueous sodium sulphate solution (3:3:10) (solvent system A) and methanol-methyl ethyl ketone-5.0% aqueous sodium sulphate solution (1:1:1) (solvent system B). Solvent system A was used for the determination of Tartrazine, Amaranth, Indigo Carmine, New Coccine, Sunset Yellow FCF, Allura Red AC, Fast Green FCF and Brilliant Blue FCF and for the screening of Acid Red (R-106), Eosin (R-103), Erythrosin (R-3), Rose Bengale (R-105) and Phloxine (R-104). When the spots of R-3, R-103, R-104, R-105 and R-106 appear on the plate, their determination can be achieved by using solvent system B. Each calibration graph was linear between 0.2 and 1.0 micrograms.

  2. Enhanced photocatalytic and adsorptive degradation of organic dyes by mesoporous Cu/Al2O3-MCM-41: intra-particle mesoporosity, electron transfer and OH radical generation under visible light.

    PubMed

    Pradhan, Amaresh C; Parida, K M; Nanda, Binita

    2011-07-28

    Mesoporous Cu/Al(2)O(3)-MCM-41 composite was synthesized by two step processes; in situ incorporation of high surface area mesoporous Al(2)O(3) (MA) into the framework of MCM-41 (in situ method) followed by impregnation of Cu(II) by incipient wetness method. The interesting thing is that starch was used for the first time as template for the preparation of high surface area MA. To evaluate the structural and electronic properties, these catalysts were characterized by low angle X-ray diffraction (LXRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-vis DRS, FTIR and photoluminescent (PL) spectra. The various cationic dye such as methylene blue (MB), methyl violet (MV), malachite green (MG) and rhodamine 6G (Rd 6G) of high concentration 500 mg L(-1) were degraded and adsorbed very efficiently (100%) using the 5 Cu/Al(2)O(3)-MCM-41 composite within 30 and 60 min, respectively. The high and quick removal of such concerted cationic organic dyes and also mixed dyes (MB+MV+MG+Rd 6G) by means of photocatalysis/adsorption is basically due to the combined effect three characteristics of synthesized mesoporous 5 Cu/Al(2)O(3)-MCM-41 composite. These characteristics are intra-particle mesoporosity, electron transfer and ˙OH radical generation under solar light. PMID:21681290

  3. Development of efficiency improved polymer-modified TiO2 for the photocatalytic degradation of an organic dye from wastewater environment

    NASA Astrophysics Data System (ADS)

    Sangareswari, Murugan; Meenakshi Sundaram, Mariappan

    2015-10-01

    In this study, the photocatalytic activity of polypyrrole-TiO2 nanocomposite was studied experimentally for the degradation of methylene blue (MB) dye under simulating solar light irradiation. To improve the photocatalytic activity of TiO2 under sunlight irradiation, conducting polymers such as polypyrrole (PPy) and its derivatives are generally used as photosensitizers. The PPy-TiO2 nanocomposite was prepared by the chemical oxidative polymerization method. The prepared nanocomposite showed better photocatalytic activity than bare TiO2 under sunlight irradiation for the degradation of MB dye. The prepared nanocomposite was subjected to characterization techniques such as SEM-EDAX, FT-IR, UV-DRS, XRD, TGA and PL spectral analysis. Different influencing operating parameters like initial concentration of dye, irradiation time, pH and amount of PPy-TiO2 nanocomposite used have also been studied. The optical density of the dye degradation was measured by UV-Visible spectrophotometer. The repeatability of photocatalytic activity was also tested. A plausible mechanism was proposed and discussed on the basis of experimental results.

  4. Organic solvent-free air-assisted liquid-liquid microextraction for optimized extraction of illegal azo-based dyes and their main metabolite from spices, cosmetics and human bio-fluid samples in one step.

    PubMed

    Barfi, Behruz; Asghari, Alireza; Rajabi, Maryam; Sabzalian, Sedigheh

    2015-08-15

    Air-assisted liquid-liquid microextraction (AALLME) has unique capabilities to develop as an organic solvent-free and one-step microextraction method, applying ionic-liquids as extraction solvent and avoiding centrifugation step. Herein, a novel and simple eco-friendly method, termed one-step air-assisted liquid-liquid microextraction (OS-AALLME), was developed to extract some illegal azo-based dyes (including Sudan I to IV, and Orange G) from food and cosmetic products. A series of experiments were investigated to achieve the most favorable conditions (including extraction solvent: 77μL of 1-Hexyl-3-methylimidazolium hexafluorophosphate; sample pH 6.3, without salt addition; and extraction cycles: 25 during 100s of sonication) using a central composite design strategy. Under these conditions, limits of detection, linear dynamic ranges, enrichment factors and consumptive indices were in the range of 3.9-84.8ngmL(-1), 0.013-3.1μgmL(-1), 33-39, and 0.13-0.15, respectively. The results showed that -as well as its simplicity, fastness, and use of no hazardous disperser and extraction solvents- OS-AALLME is an enough sensitive and efficient method for the extraction of these dyes from complex matrices. After optimization and validation, OS-AALLME was applied to estimate the concentration of 1-amino-2-naphthol in human bio-fluids as a main reductive metabolite of selected dyes. Levels of 1-amino-2-naphthol in plasma and urinary excretion suggested that this compound may be used as a new potential biomarker of these dyes in human body. PMID:26149246

  5. Organic solvent-free air-assisted liquid-liquid microextraction for optimized extraction of illegal azo-based dyes and their main metabolite from spices, cosmetics and human bio-fluid samples in one step.

    PubMed

    Barfi, Behruz; Asghari, Alireza; Rajabi, Maryam; Sabzalian, Sedigheh

    2015-08-15

    Air-assisted liquid-liquid microextraction (AALLME) has unique capabilities to develop as an organic solvent-free and one-step microextraction method, applying ionic-liquids as extraction solvent and avoiding centrifugation step. Herein, a novel and simple eco-friendly method, termed one-step air-assisted liquid-liquid microextraction (OS-AALLME), was developed to extract some illegal azo-based dyes (including Sudan I to IV, and Orange G) from food and cosmetic products. A series of experiments were investigated to achieve the most favorable conditions (including extraction solvent: 77μL of 1-Hexyl-3-methylimidazolium hexafluorophosphate; sample pH 6.3, without salt addition; and extraction cycles: 25 during 100s of sonication) using a central composite design strategy. Under these conditions, limits of detection, linear dynamic ranges, enrichment factors and consumptive indices were in the range of 3.9-84.8ngmL(-1), 0.013-3.1μgmL(-1), 33-39, and 0.13-0.15, respectively. The results showed that -as well as its simplicity, fastness, and use of no hazardous disperser and extraction solvents- OS-AALLME is an enough sensitive and efficient method for the extraction of these dyes from complex matrices. After optimization and validation, OS-AALLME was applied to estimate the concentration of 1-amino-2-naphthol in human bio-fluids as a main reductive metabolite of selected dyes. Levels of 1-amino-2-naphthol in plasma and urinary excretion suggested that this compound may be used as a new potential biomarker of these dyes in human body.

  6. Monitoring the dye impregnation time of nanostructured photoanodes for dye sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Shahzad, N.; Pugliese, D.; Lamberti, A.; Sacco, A.; Virga, A.; Gazia, R.; Bianco, S.; Shahzad, M. I.; Tresso, E.; Pirri, C. F.

    2013-06-01

    Dye-sensitized solar cells (DSSCs) are getting increasing attention as low-cost, easy-to-prepare and colored photovoltaic devices. In the current work, in view of optimizing the fabrication procedures and understanding the mechanisms of dye attachment to the semiconductor photoanode, absorbance measurements have been performed at different dye impregnation times ranging from few minutes to 24 hours using UV-Vis spectroscopy. In addition to the traditional absorbance experiments, based on diffuse and specular reflectance on dye impregnated thin films and on the desorption of dye molecules from the photoanodes by means of a basic solution, an alternative in-situ solution depletion measurement, which enables fast and continuous evaluation of dye uptake, is presented. Photoanodes have been prepared with two different nanostructured semiconducting films: mesoporous TiO2, using a commercially available paste from Solaronix, and sponge-like ZnO obtained in our laboratory from sputtering and thermal annealing. Two different dyes have been analyzed: Ruthenizer 535-bisTBA (N719), which is widely used because it gives optimal photovoltaic performances, and a new metal-free organic dye based on a hemisquaraine molecule (CT1). Dye sensitized cells were fabricated using a customized microfluidic architecture. The results of absorbance measurements are presented and discussed in relation to the obtained solar energy conversion efficiencies and the incident photon-to-electron conversion efficiencies (IPCE).

  7. Role of white rot fungus Funalia trogii in detoxification of textile dyes.

    PubMed

    Apohan, Elif; Yesilada, Ozfer

    2005-01-01

    Toxic and genotoxic effects of the textile dyes on organisms suggest the need for remediation of dyes before discharging them into the environment. For this reason, the ability of Funalia trogii pellets to detoxify textile dyes was investigated and evaluated. Although, textile dyes are toxic substances for many microorganisms, the pellets were able to decolorize and detoxify the azo dyes used. Astrazon Blue and Red dyes inhibit growth of F. trogii and S. aureus on solid medium in a concentration dependent manner. The toxicity of these dyes on a fungus, F. trogii and a bacterium, S. aureus was significantly decreased after pretreatment with fungal pellets.

  8. Laser ablation of dyes

    NASA Astrophysics Data System (ADS)

    Späth, M.; Stuke, M.

    1992-01-01

    High density 50 μs pulses of the UV dyes PPF, POPOP and BBO and of two dyes in the visible region, Xanthen N92 and Fluorol 7GA were generated by laser ablation. Dye powders were pressed with 7800 kp/cm 2 in round pellets which were ablated by exposure to KrF excimer laser radiation (248 nm) at a fluence of 100 mJ/cm 2. The ablation cloud was optically activated with a XeCl excimer laser. Its fluorescence spectrum was measured and was identified as a dye vapour fluorescence spectrum by comparison to conventional dye solution and dye vapour spectra. The dye cloud is not deflected in an electric field (10 6 V/m). By changing the delay time between the ablation laser and the focused activation laser, the velocity distribution of the ablated dye was measured. Its maximum is at 600 m/s for PPF. Knowing the thickness of the ablated dye layer per shot (300 Å) and the size of the ablation cloud (pictures of a video camera), one can estimate the maximum density of the dye in the gas pulse to be 10 -5 mol/ l in the range of concentration of lasing dyes. However, no lasing was observed up to now.

  9. Synthesis of azoimidazolium dyes with nitrous oxide.

    PubMed

    Tskhovrebov, Alexander G; Naested, Lara C E; Solari, Euro; Scopelliti, Rosario; Severin, Kay

    2015-01-19

    A new method for the synthesis of industrially important azoimidazolium dyes is presented. The procedure is based on a reagent which is rarely used in the context of synthetic organic chemistry: nitrous oxide ("laughing gas"). N2O is first coupled to N-heterocyclic carbenes. Subsequent reaction with aromatic compounds through an AlCl3-induced C-H activation process provides azoimidazolium dyes in good yields. PMID:25420599

  10. Preparation of Nanoporous TiO2 for Dye-Sensitized Solar Cell (DSSC) Using Various Dyes

    NASA Astrophysics Data System (ADS)

    Yuliarto, Brian; Fanani, Fahiem; Fuadi, M. Kasyful; Nugraha

    2010-10-01

    This article reports the development of organic dyes as an attempt to reduce material costs of Dye-Sensitized Solar Cell (DSSC). Indonesia, a country with variety and considerable number of botanical resources, is suitable to perform the research. Indonesian black rice, curcuma, papaya leaf, and the combination were chosen as organic dyes source. Dyes were extracted using organic solvent and adsorbed on mesoporous Titanium Dioxide (TiO2) which has been optimized in our laboratory. The best dyes light absorbance and performance obtained from papaya leaf as chlorophyll dyes that gives two peaks at 432 nm and 664 nm from UV-Vis Spectrophotometry and performance under 100 mW/cm2 Xenon light solar simulator gives VOC = 0.566 Volt, JSC = 0.24 mA/cm2, Fill Factor = 0.33, and efficiency of energy conversion 0,045%.

  11. Ultrasonic dyeing of cellulose nanofibers.

    PubMed

    Khatri, Muzamil; Ahmed, Farooq; Jatoi, Abdul Wahab; Mahar, Rasool Bux; Khatri, Zeeshan; Kim, Ick Soo

    2016-07-01

    Textile dyeing assisted by ultrasonic energy has attained a greater interest in recent years. We report ultrasonic dyeing of nanofibers for the very first time. We chose cellulose nanofibers and dyed with two reactive dyes, CI reactive black 5 and CI reactive red 195. The cellulose nanofibers were prepared by electrospinning of cellulose acetate (CA) followed by deacetylation. The FTIR results confirmed complete conversion of CA into cellulose nanofibers. Dyeing parameters optimized were dyeing temperature, dyeing time and dye concentrations for each class of the dye used. Results revealed that the ultrasonic dyeing produced higher color yield (K/S values) than the conventional dyeing. The color fastness test results depicted good dye fixation. SEM analysis evidenced that ultrasonic energy during dyeing do not affect surface morphology of nanofibers. The results conclude successful dyeing of cellulose nanofibers using ultrasonic energy with better color yield and color fastness results than conventional dyeing. PMID:26964959

  12. Ultrasonic dyeing of cellulose nanofibers.

    PubMed

    Khatri, Muzamil; Ahmed, Farooq; Jatoi, Abdul Wahab; Mahar, Rasool Bux; Khatri, Zeeshan; Kim, Ick Soo

    2016-07-01

    Textile dyeing assisted by ultrasonic energy has attained a greater interest in recent years. We report ultrasonic dyeing of nanofibers for the very first time. We chose cellulose nanofibers and dyed with two reactive dyes, CI reactive black 5 and CI reactive red 195. The cellulose nanofibers were prepared by electrospinning of cellulose acetate (CA) followed by deacetylation. The FTIR results confirmed complete conversion of CA into cellulose nanofibers. Dyeing parameters optimized were dyeing temperature, dyeing time and dye concentrations for each class of the dye used. Results revealed that the ultrasonic dyeing produced higher color yield (K/S values) than the conventional dyeing. The color fastness test results depicted good dye fixation. SEM analysis evidenced that ultrasonic energy during dyeing do not affect surface morphology of nanofibers. The results conclude successful dyeing of cellulose nanofibers using ultrasonic energy with better color yield and color fastness results than conventional dyeing.

  13. Study on the fluorescence enhancement in Lanthanum(III)-carminic acid-cetyltrimethylammonium bromide system and its analytical application.

    PubMed

    Wang, Feng; Huang, Wei; Li, Kexiang; Li, Aihua; Gao, Wei; Tang, Bo

    2011-09-01

    A fluorescent enhancement system carminic acid (CA)-La3+-CTAB is found and based on this finding a new fluorimetric method for the determination of CA is developed. Under optimized conditions, the enhanced intensities of fluorescence are quantitatively in proportion to the concentrations of CA in the range of 0.01231-12.31 μg mL(-1). The detection limit is 10.92 ng mL(-1). Compared with other methods that have been reported to determine CA, this method has high sensitivity, stability and wide linear range. In addition, the luminescence mechanism indicates that the complex of La3+-CA (1:2) forms and solubilizes in CTAB micelle. PMID:21703912

  14. Study on the fluorescence enhancement in Lanthanum(III)-carminic acid-cetyltrimethylammonium bromide system and its analytical application

    NASA Astrophysics Data System (ADS)

    Wang, Feng; Huang, Wei; Li, Kexiang; Li, Aihua; Gao, Wei; Tang, Bo

    2011-09-01

    A fluorescent enhancement system carminic acid (CA)-La 3+-CTAB is found and based on this finding a new fluorimetric method for the determination of CA is developed. Under optimized conditions, the enhanced intensities of fluorescence are quantitatively in proportion to the concentrations of CA in the range of 0.01231-12.31 μg mL -1. The detection limit is 10.92 ng mL -1. Compared with other methods that have been reported to determine CA, this method has high sensitivity, stability and wide linear range. In addition, the luminescence mechanism indicates that the complex of La 3+-CA (1:2) forms and solubilizes in CTAB micelle.

  15. Plasma induced degradation of Indigo Carmine by bipolar pulsed dielectric barrier discharge(DBD) in the water-air mixture.

    PubMed

    Zhang, Ruo-Bing; Wu, Yan; Li, Guo-Feng; Wang, Ning-Hui; Li, Jie

    2004-01-01

    Degradation of the Indigo Carmine (IC) by the bipolar pulsed DBD in water-air mixture was studied. Effects of various parameters such as gas flow rate, solution conductivity, pulse repetitive rate and ect., on color removal efficiency of dying wastewater were investigated. Concentrations of gas phase o3 and aqueous phase H2O2 under various conditions were measured. Experimental results showed that air bubbling facilitates the breakdown of water and promotes generation of chemically active species. Color removal efficiency of IC solution can be greatly improved by the air aeration under various solution conductivities. Decolorization efficiency increases with the increase of the gas flow rate, and decreases with the increase of the initial solution conductivity. A higher pulse repetitive rate and a larger pulse capacitor C(p) are favorable for the decolorization process. Ozone and hydrogen peroxide formed decreases with the increase of initial solution conductivity. In addition, preliminary analysis of the decolorization mechanisms is given.

  16. Effect of mercerization and gamma irradiation on the dyeing behaviour of cotton using stilbene based direct dye

    NASA Astrophysics Data System (ADS)

    Bhatti, Ijaz Ahmad; Adeel, Shahid; Fazal-ur-Rehman; Irshad, Misbah; Abbas, Muhammad

    2012-07-01

    The dyeing behaviour of mercerized and gamma irradiated cotton fabric using stilbene based direct dye has been investigated. The fabric was treated with different concentrations of alkali to optimize the mercerization. The optimum mercerized cotton fabric was irradiated to absorbed doses of 2, 4, 6, 8 and 10 kGy using Cs-137 gamma irradiator. Dyeing was performed using irradiated and un-irradiated cotton with dye solutions. The dyeing parameters such as temperature, time of dyeing, pH of dyeing solutions and salt concentration were optimized. The colour strength values of dyed fabrics were evaluated by comparing irradiated and un-irradiated cotton in CIE Lab system using Spectra flash SF650. Methods suggested by International Standard Organization (ISO) were employed to study the effect of gamma irradiation on the colourfastness properties of dyed fabric. It was found that mercerized and irradiated cotton have not only improved the colour strength but enhanced the rating of fastness properties also.

  17. Organic Photosensitizers Incorporating Rigidified Dithieno[3,2-f:2',3'-h]quinoxaline Segment Tethered with Thiophene Substitutes for Dye-Sensitized Solar Cells.

    PubMed

    Ni, Jen-Shyang; Chiu, Tang-Yao; Kao, Wei-Siang; Chou, Hao-Ju; Su, Chao-Chin; Lin, Jiann T

    2016-09-01

    Metal-free D-π-RS-π-A type sensitizers, consisting of triphenylamine as the electron donor, 2,3-bis(3-(2-ethylhexyl)-5-methylthiophen-2-yl)dithieno[3,2-f:2',3'-h]quinoxaline (DTQT) as the rigidified conjugation spacer (RS), thiophene as the π-spacer, and 2-cyanoacrylic acid as the acceptor/anchor, have broad absorption spectra ranging from 350 to 550 nm and a high molar extinction coefficient up to >46 200 M(-1) cm(-1). Under simulated AM 1.5 G illumination, the dye-sensitized solar cells (DSSCs) fabricated from the dyes exhibited light-to-electricity conversions in the range of 6.78% to 8.27%. The best efficiency is slightly higher than that of N719-based standard DSSC (7.92%). The efficiency can be further boosted to 8.51% by optimizing the concentration of LiI electrolyte. PMID:27523392

  18. Two photon absorption energy transfer in the light-harvesting complex of photosystem II (LHC-II) modified with organic boron dye.

    PubMed

    Chen, Li; Liu, Cheng; Hu, Rui; Feng, Jiao; Wang, Shuangqing; Li, Shayu; Yang, Chunhong; Yang, Guoqiang

    2014-07-15

    The plant light-harvesting complexes of photosystem II (LHC-II) play important roles in collecting solar energy and transferring the energy to the reaction centers of photosystems I and II. A two photon absorption compound, 4-(bromomethyl)-N-(4-(dimesitylboryl)phenyl)-N-phenylaniline (DMDP-CH2Br), was synthesized and covalently linked to the LHC-II in formation of a LHC-II-dye complex, which still maintained the biological activity of LHC-II system. Under irradiation with femtosecond laser pulses at 754 nm, the LHC-II-dye complex can absorb two photons of the laser light effectively compared with the wild type LHC-II. The absorbed excitation energy is then transferred to chlorophyll a with an obvious fluorescence enhancement. The results may be interesting and give potentials for developing hybrid photosystems.

  19. Organic Photosensitizers Incorporating Rigidified Dithieno[3,2-f:2',3'-h]quinoxaline Segment Tethered with Thiophene Substitutes for Dye-Sensitized Solar Cells.

    PubMed

    Ni, Jen-Shyang; Chiu, Tang-Yao; Kao, Wei-Siang; Chou, Hao-Ju; Su, Chao-Chin; Lin, Jiann T

    2016-09-01

    Metal-free D-π-RS-π-A type sensitizers, consisting of triphenylamine as the electron donor, 2,3-bis(3-(2-ethylhexyl)-5-methylthiophen-2-yl)dithieno[3,2-f:2',3'-h]quinoxaline (DTQT) as the rigidified conjugation spacer (RS), thiophene as the π-spacer, and 2-cyanoacrylic acid as the acceptor/anchor, have broad absorption spectra ranging from 350 to 550 nm and a high molar extinction coefficient up to >46 200 M(-1) cm(-1). Under simulated AM 1.5 G illumination, the dye-sensitized solar cells (DSSCs) fabricated from the dyes exhibited light-to-electricity conversions in the range of 6.78% to 8.27%. The best efficiency is slightly higher than that of N719-based standard DSSC (7.92%). The efficiency can be further boosted to 8.51% by optimizing the concentration of LiI electrolyte.

  20. Two photon absorption energy transfer in the light-harvesting complex of photosystem II (LHC-II) modified with organic boron dye

    NASA Astrophysics Data System (ADS)

    Chen, Li; Liu, Cheng; Hu, Rui; Feng, Jiao; Wang, Shuangqing; Li, Shayu; Yang, Chunhong; Yang, Guoqiang

    2014-07-01

    The plant light-harvesting complexes of photosystem II (LHC-II) play important roles in collecting solar energy and transferring the energy to the reaction centers of photosystems I and II. A two photon absorption compound, 4-(bromomethyl)-N-(4-(dimesitylboryl)phenyl)-N-phenylaniline (DMDP-CH2Br), was synthesized and covalently linked to the LHC-II in formation of a LHC-II-dye complex, which still maintained the biological activity of LHC-II system. Under irradiation with femtosecond laser pulses at 754 nm, the LHC-II-dye complex can absorb two photons of the laser light effectively compared with the wild type LHC-II. The absorbed excitation energy is then transferred to chlorophyll a with an obvious fluorescence enhancement. The results may be interesting and give potentials for developing hybrid photosystems.

  1. Modification of TiO₂ electrode with organic silane interposed layer for high-performance of dye-sensitized solar cells.

    PubMed

    Sewvandi, Galhenage A; Tao, Zhuoqi; Kusunose, Takafumi; Tanaka, Yasuhiro; Nakanishi, Shunsuke; Feng, Qi

    2014-04-23

    Back electron transfer from the TiO2 electrode surface to the electrolyte is the main reason behind the low-open circuit potential (Voc) and the low-fill factor (FF) of the dye-sensitized solar cells (DSSCs). Modifications to the TiO2 electrode, fabricated using {010}-faceted TiO2 nanoparticles with six different kinds of silane, are reported to decrease the back electron transfer on the TiO2 surface. The effect of alkyl chain length of hydrocarbon silanes and fluorocarbon silanes on adsorption parameters of surface coverage and adsorption constant, interfacial resistance, and photovoltaic performances were investigated. Adsorption isotherms, impedance analysis, and photovoltaic measurements were used as the investigation techniques. The reduction of back electron transfer depended on the TiO2 surface coverage by silane, alkyl chain length, and the molecular structure of the silane. Even though Voc and FF were improved, significant reduction in short-circuit photocurrent density (Jsc) was observed after silanization because of desorption of dye during silanization. A new approach, sequential adsorption process of silane and dye, was introduced to enhance Voc and FF without lowering Jsc. Heptadecafluorodecyl trimethoxy-silane showed the highest coverage on the surface of the TiO2 and had the highest effect on the performance improvement of the DSSC, where Voc, FF, and efficiency (η) were improved by 22, 8.0, and 22%, respectively.

  2. Efficiency Records in Mesoscopic Dye-Sensitized Solar Cells.

    PubMed

    Albero, Josep; Atienzar, Pedro; Corma, Avelino; Garcia, Hermenegildo

    2015-08-01

    The aim of the present review article is to show the progress achieved in the efficiency of dye-sensitized solar cells (DSSCs) by evolution in the structure and composition of the dye. After an initial brief description of DSSCs and the operating mechanism the major part of the present article is organized according to the type of dye, trying to show the logic in the variation of the dye structure in order to achieve strong binding on the surface of the layer of nanoparticulate TiO2 , efficient interfacial electron injection between the excited dye and the semiconductor, and minimization of the unwanted dark current processes. Besides metal complexes, including polypyridyls and nitrogenated macro rings, organic dyes and inorganic light harvesters such as quantum dots and perovskites have also been included in the review. The last section summarizes the current state of the art and provides an overview on future developments in the field. PMID:26183911

  3. Efficiency Records in Mesoscopic Dye-Sensitized Solar Cells.

    PubMed

    Albero, Josep; Atienzar, Pedro; Corma, Avelino; Garcia, Hermenegildo

    2015-08-01

    The aim of the present review article is to show the progress achieved in the efficiency of dye-sensitized solar cells (DSSCs) by evolution in the structure and composition of the dye. After an initial brief description of DSSCs and the operating mechanism the major part of the present article is organized according to the type of dye, trying to show the logic in the variation of the dye structure in order to achieve strong binding on the surface of the layer of nanoparticulate TiO2 , efficient interfacial electron injection between the excited dye and the semiconductor, and minimization of the unwanted dark current processes. Besides metal complexes, including polypyridyls and nitrogenated macro rings, organic dyes and inorganic light harvesters such as quantum dots and perovskites have also been included in the review. The last section summarizes the current state of the art and provides an overview on future developments in the field.

  4. Detoxification of azo dyes in the context of environmental processes.

    PubMed

    Rawat, Deepak; Mishra, Vandana; Sharma, Radhey Shyam

    2016-07-01

    Azo dyes account for >70% of the global industrial demand (∼9 million tons). Owing to their genotoxic/carcinogenic potential, the annual disposal of ∼4,500,000 tons of dyes and/or degraded products is an environmental and socio-economic concern. In comparison to physico-chemical methods, microbe-mediated dye degradation is considered to be low-input, cost-effective and environmentally-safe. However, under different environmental conditions, interactions of chemically diverse dyes with metabolically diverse microbes produce metabolites of varying toxicity. In addition, majority of studies on microbial dye-degradation focus on decolorization with least attention towards detoxification. Therefore, the environmental significance of microbial dye detoxification research of past >3 decades is critically evaluated with reference to dye structure and the possible influence of microbial interactions in different environments. In the absence of ecosystem-based studies, the results of laboratory-based studies on dye degradation, metabolite production and their genotoxic impact on model organisms are used to predict the possible fate and consequences of azo dyes/metabolites in the environment. In such studies, the predominance of fewer numbers of toxicological assays that too at lower levels of biological organization (molecular/cellular/organismic) suggests its limited ecological significance. Based on critical evaluation of these studies the recommendations on inclusion of multilevel approach (assessment at multiple levels of biological organization), multispecies microcosm approach and native species approach in conjunction with identification of dye metabolites have been made for future studies. Such studies will bridge the gap between the fundamental knowledge on dye-microbe-environment interactions and its application to combat dye-induced environmental toxicity. Thus an environmental perspective on dye toxicity in the background of dye structure and effects of

  5. Detoxification of azo dyes in the context of environmental processes.

    PubMed

    Rawat, Deepak; Mishra, Vandana; Sharma, Radhey Shyam

    2016-07-01

    Azo dyes account for >70% of the global industrial demand (∼9 million tons). Owing to their genotoxic/carcinogenic potential, the annual disposal of ∼4,500,000 tons of dyes and/or degraded products is an environmental and socio-economic concern. In comparison to physico-chemical methods, microbe-mediated dye degradation is considered to be low-input, cost-effective and environmentally-safe. However, under different environmental conditions, interactions of chemically diverse dyes with metabolically diverse microbes produce metabolites of varying toxicity. In addition, majority of studies on microbial dye-degradation focus on decolorization with least attention towards detoxification. Therefore, the environmental significance of microbial dye detoxification research of past >3 decades is critically evaluated with reference to dye structure and the possible influence of microbial interactions in different environments. In the absence of ecosystem-based studies, the results of laboratory-based studies on dye degradation, metabolite production and their genotoxic impact on model organisms are used to predict the possible fate and consequences of azo dyes/metabolites in the environment. In such studies, the predominance of fewer numbers of toxicological assays that too at lower levels of biological organization (molecular/cellular/organismic) suggests its limited ecological significance. Based on critical evaluation of these studies the recommendations on inclusion of multilevel approach (assessment at multiple levels of biological organization), multispecies microcosm approach and native species approach in conjunction with identification of dye metabolites have been made for future studies. Such studies will bridge the gap between the fundamental knowledge on dye-microbe-environment interactions and its application to combat dye-induced environmental toxicity. Thus an environmental perspective on dye toxicity in the background of dye structure and effects of

  6. A metal-free N-annulated thienocyclopentaperylene dye: power conversion efficiency of 12% for dye-sensitized solar cells.

    PubMed

    Yao, Zhaoyang; Zhang, Min; Li, Renzhi; Yang, Lin; Qiao, Yongna; Wang, Peng

    2015-05-11

    Reported are two highly efficient metal-free perylene dyes featuring N-annulated thienobenzoperylene (NTBP) and N-annulated thienocyclopentaperylene (NTCP), which are coplanar polycyclic aromatic hydrocarbons. Without the use of any coadsorbate, the metal-free organic dye derived from the NTCP segment was used for a dye-sensitized solar cell which attained a power conversion efficiency of 12% under an irradiance of 100 mW cm(-2), simulated air mass global (AM1.5G) sunlight.

  7. Enhancement of solar light photocatalytic activity of TiO2-CeO2 composite by Er3+:Y3Al5O12 in organic dye degradation

    NASA Astrophysics Data System (ADS)

    Li, Y.; Li, S. G.; Zhang, L.; Wang, J.; Li, Y.; Ma, C. H.

    2014-12-01

    The Er3+:Y3Al5O12, as an upconversion luminescence agent which is able to transform the visible part of the solar light to ultraviolet light, was prepared by nitrate-citrate sol-gel method. A novel solar light photocatalyst, Er3+:Y3Al5O12/TiO2-CeO2 composite was synthesized using ultrasonic treatment. The X-ray diffraction (XRD) and scanning election microscopy (SEM) were used to characterize the structural morphology of the Er3+:Y3Al5O12/TiO2-CeO2 composite. In order to evaluate the solar light photocatalytic activity of Er3+:Y3Al5O12/TiO2-CeO2 composite, the Azo Fuchsine dye was used as a model organic pollutant. The progress of the degradation reaction was monitored by UV-Vis spectroscopy and ion chromatography. The key influences on the solar light photocatalytic activity of Er3+:Y3Al5O12/TiO2-CeO2 were studied, such as Ti/Ce molar ratio, heat-treatment temperature and heat-treatment time. Otherwise, the effects of initial dye concentration, Er3+:Y3Al5O12/TiO2-CeO2 amount, solar light irradiation time and the nature of the dye on the solar light photocatalytic degradation process were investigated. It was found that the solar light photocatalytic activity of Er3+:Y3Al5O12/TiO2-CeO2 composite was superior to Er3+:Y3Al5O12/TiO2 and Er3+:Y3Al5O12/CeO2 powder in the similar conditions.

  8. Recyclability of thin nylon film-supported p-CuBiS2/ n-TiO2 heterojunction-based nanocomposites for visible light photocatalytic degradation of organic dye

    NASA Astrophysics Data System (ADS)

    Abdullah, Hairus; Kuo, Dong-Hau; Lee, Jiunn-Yih; Wu, Chang-Mou

    2016-08-01

    Hybrid film photocatalysts have been prepared by embedding SiO2/TiO2/CuBiS2/Ag nanocomposite spheres into nylon films (nylon/catalyst) for controlling the leaching problem of catalyst powders during the photodegradation of acid black 1 (AB 1) dye solution. The composite catalyst with 500 nm SiO2 sphere as a support which had uniform size and shape was synthesized by the sol-gel and hydrothermal methods. The coupling between p-CuBiS2 and n-TiO2 nanoparticles showed synergetic effects to the enhancement of organic dye photodegradation under visible light irradiation. Furthermore, the Ag nanoparticles on the nanocomposites increased the surface plasmonic resonance and acted as electron trapping which is leading to better photocarrier separation. The 20, 30, and 40 mg as-prepared nanocomposite catalysts were embedded into nylon films to produce three different compositions of 120 mg nylon/catalyst hybrids. The good photodegradation property of 40 mg nylon/catalyst hybrid was tested and was found that it could degrade the 100 mL of 5 ppm dye solution, respectively, in 150, 120, 180, and 150 min in four consecutive runs under 150 W halogen light irradiation. The hybrid films did not need a washing procedure after being used and could be incessantly used after that. The good reusability of hybrid photocatalyst films is attributed to its porosity, thin thickness, tiny size of nanoparticles (less than 10 nm), and the formation of nano p- n diodes between p-CuBiS2 and n-TiO2 nanoparticles.

  9. Toxicity of xanthene food dyes by inhibition of human drug-metabolizing enzymes in a noncompetitive manner.

    PubMed

    Mizutani, Takaharu

    2009-01-01

    The synthetic food dyes studied were rose bengal (RB), phroxine (PL), amaranth, erythrosine B (ET), allura red, new coccine, acid red (AR), tartrazine, sunset yellow FCF, brilliant blue FCF, and indigo carmine. First, data confirmed that these dyes were not substrates for CYP2A6, UGT1A6, and UGT2B7. ET inhibited UGT1A6 (glucuronidation of p-nitrophenol) and UGT2B7 (glucuronidation of androsterone). We showed the inhibitory effect of xanthene dye on human UGT1A6 activity. Basic ET, PL, and RB in those food dyes strongly inhibited UGT1A6 activity, with IC(50) values = 0.05, 0.04, and 0.015 mM, respectively. Meanwhile, AR of an acidic xanthene food dye showed no inhibition. Next, we studied the inhibition of CYP3A4 of a major phase I drug-metabolizing enzyme and P-glycoprotein of a major transporter by synthetic food dyes. Human CYP3A4 and P-glycoprotein were also inhibited by basic xanthene food dyes. The IC(50) values of these dyes to inhibit CYP3A4 and P-glycoprotein were the same as the inhibition level of UGT1A6 by three halogenated xanthene food dyes (ET, PL, and RB) described above, except AR, like the results with UGT1A6 and UGT2B7. We also confirmed the noninhibition of CYP3A4 and P-gp by other synthetic food dyes. Part of this inhibition depended upon the reaction of (1)O(2) originating on xanthene dyes by light irradiation, because inhibition was prevented by (1)O(2) quenchers. We studied the influence of superoxide dismutase and catalase on this inhibition by dyes and we found prevention of inhibition by superoxide dismutase but not catalase. This result suggests that superoxide anions, originating on dyes by light irradiation, must attack drug-metabolizing enzymes. It is possible that red cosmetics containing phloxine, erythrosine, or rose bengal react with proteins on skin under lighting and may lead to rough skin.

  10. Toxicity of Xanthene Food Dyes by Inhibition of Human Drug-Metabolizing Enzymes in a Noncompetitive Manner

    PubMed Central

    Mizutani, Takaharu

    2009-01-01

    The synthetic food dyes studied were rose bengal (RB), phroxine (PL), amaranth, erythrosine B (ET), allura red, new coccine, acid red (AR), tartrazine, sunset yellow FCF, brilliant blue FCF, and indigo carmine. First, data confirmed that these dyes were not substrates for CYP2A6, UGT1A6, and UGT2B7. ET inhibited UGT1A6 (glucuronidation of p-nitrophenol) and UGT2B7 (glucuronidation of androsterone). We showed the inhibitory effect of xanthene dye on human UGT1A6 activity. Basic ET, PL, and RB in those food dyes strongly inhibited UGT1A6 activity, with IC50 values = 0.05, 0.04, and 0.015 mM, respectively. Meanwhile, AR of an acidic xanthene food dye showed no inhibition. Next, we studied the inhibition of CYP3A4 of a major phase I drug-metabolizing enzyme and P-glycoprotein of a major transporter by synthetic food dyes. Human CYP3A4 and P-glycoprotein were also inhibited by basic xanthene food dyes. The IC50 values of these dyes to inhibit CYP3A4 and P-glycoprotein were the same as the inhibition level of UGT1A6 by three halogenated xanthene food dyes (ET, PL, and RB) described above, except AR, like the results with UGT1A6 and UGT2B7. We also confirmed the noninhibition of CYP3A4 and P-gp by other synthetic food dyes. Part of this inhibition depended upon the reaction of 1O2 originating on xanthene dyes by light irradiation, because inhibition was prevented by 1O2 quenchers. We studied the influence of superoxide dismutase and catalase on this inhibition by dyes and we found prevention of inhibition by superoxide dismutase but not catalase. This result suggests that superoxide anions, originating on dyes by light irradiation, must attack drug-metabolizing enzymes. It is possible that red cosmetics containing phloxine, erythrosine, or rose bengal react with proteins on skin under lighting and may lead to rough skin. PMID:20041016

  11. Comparison of the ionizing radiation effects on cochineal, annatto and turmeric natural dyes

    NASA Astrophysics Data System (ADS)

    Cosentino, Helio M.; Takinami, Patricia Y. I.; del Mastro, Nelida L.

    2016-07-01

    As studies on radiation stability of food dyes are scarce, commercially important natural food grade dyes were evaluated in terms of their sensitivity against gamma ionizing radiation. Cochineal, annatto and turmeric dyes with suitable concentrations were subjected to increasing doses up to 32 kGy and analyzed by spectrophotometry and capillary electrophoresis. The results showed different pattern of absorbance versus absorbed dose for the three systems. Carmine, the glucosidal coloring matter from the scale insect Coccus cacti L., Homoptera (cochineal) remained almost unaffected by radiation up to doses of about 32 kGy (absorbance at 494 nm). Meanwhile, at that dose, a plant-derived product annatto or urucum (Bixa orellana L.) tincture presented a nearly 58% reduction in color intensity. Tincture of curcumin (diferuloylmethane) the active ingredient in the eastern spice turmeric (Curcuma longa) showed to be highly sensitive to radiation when diluted. These data shall be taken in account whenever food products containing these food colors were going to undergo radiation processing.

  12. Chitosan-based hydrogel for dye removal from aqueous solutions: Optimization of the preparation procedure

    NASA Astrophysics Data System (ADS)

    Gioiella, Lucia; Altobelli, Rosaria; de Luna, Martina Salzano; Filippone, Giovanni

    2016-05-01

    The efficacy of chitosan-based hydrogels in the removal of dyes from aqueous solutions has been investigated as a function of different parameters. Hydrogels were obtained by gelation of chitosan with a non-toxic gelling agent based on an aqueous basic solution. The preparation procedure has been optimized in terms of chitosan concentration in the starting solution, gelling agent concentration and chitosan-to-gelling agent ratio. The goal is to properly select the material- and process-related parameters in order to optimize the performances of the chitosan-based dye adsorbent. First, the influence of such factors on the gelling process has been studied from a kinetic point of view. Then, the effects on the adsorption capacity and kinetics of the chitosan hydrogels obtained in different conditions have been investigated. A common food dye (Indigo Carmine) has been used for this purpose. Noticeably, although the disk-shaped hydrogels are in the bulk form, their adsorption capacity is comparable to that reported in the literature for films and beads. In addition, the bulk samples can be easily separated from the liquid phase after the adsorption process, which is highly attractive from a practical point of view. Compression tests reveal that the samples do not breakup even after relatively large compressive strains. The obtained results suggest that the fine tuning of the process parameters allows the production of mechanical resistant and highly adsorbing chitosan-based hydrogels.

  13. Resistance status of the carmine spider mite, Tetranychus cinnabarinus and the twospotted spider mite, Tetranychus urticae to selected acaricides on strawberries.

    PubMed

    Bi, Jian-Long; Niu, Zi-Mian; Yu, Lu; Toscano, Nick C

    2016-02-01

    The carmine spider mite, Tetranychus cinnabarinus (Boisduval) and the twospotted spider mite, Tetranychus urticae Koch, are serious pests of strawberries and many other horticultural crops. Control of these pests has been heavily dependent upon chemical acaricides. Objectives of this study were to determine the resistance status of these two pest species to commonly used acaricides on strawberries in a year-round intensive horticultural production region. LC90 of abamectin for adult carmine spider mites was 4% whereas that for adult twospotted spider mites was 24% of the top label rate. LC90s of spiromesifen, etoxazole, hexythiazox and bifenazate were 0.5%, 0.5%, 1.4% and 83% of their respective highest label rates for carmine spider mite eggs, 0.7%, 2.7%, 12.1% and 347% of their respective highest label rates for the nymphs. LC90s of spiromesifen, etoxazole, hexythiazox and bifenazate were 4.6%, 11.1%, 310% and 62% of their respective highest label rates for twospotted spider mite eggs, 3%, 13%, 432,214% and 15% of their respective highest label rates for the nymphs. Our results suggest that T. cinnabarinus have developed resistance to bifenazate and that the T. urticae have developed resistance to hexythiazox. These results strongly emphasize the need to develop resistance management strategies in the region.

  14. One-pot synthesis of ZnO2/ZnO composite with enhanced photocatalytic performance for organic dye removal.

    PubMed

    Liu, Wei; Wang, Mingliang; Xu, Chunxiang; Chen, Shifu; Fu, Xianliang

    2013-01-01

    The ZnO2/ZnO photocatalysts with various ZnO2 contents were prepared by one-pot synthesis method using ZnO and H2O2 as raw materials. The photocatalysts were characterized by XRD, UV-vis DRS, SEM, EDS, FT-IR spectra, fluorescence emission spectra, and BET specific area. The photocatalytic performance of the photocatalyst was evaluated by photocatalytic degradation of methyl orange (MO) and rhodamine B (RhB). The results showed that the photocatalytic activity of the ZnO2/ZnO was much higher than that of single-phase ZnO or ZnO2. The optimum ZnO2 content was 1.0 wt.%. The maximal degradation rate constant of MO and RhB was 4.1 times and 2.2 times that observed for pure ZnO, respectively. The stability of the prepared photocatalyst in the photocatalytic process was also investigated. The active species in dye degradation were examined by adding a series of scavengers. The possible mechanisms involved in the photocatalytic degradation of dye were also discussed.

  15. Synthesis and photocatalytic oxidation of different organic dyes by using Mn 2O 3/TiO 2 solid solution and visible light

    NASA Astrophysics Data System (ADS)

    Ghorai, Tanmay K.; Pramanik, Susmita; Pramanik, Panchanan

    2009-08-01

    Mn 2O 3/TiO 2 solid solution was prepared from two different oxides, manganese oxide (from KMnO 4 and ethanol) and TiO 2, these samples were characterized by BET, XRD, EDAX, SEM, FT-IR, ESR, XPS and UV-vis absorption spectroscopy. Photocatalytic activities of Mn 2O 3/TiO 2 powder was investigated by photooxidation of different dyes like Rhodamine B, thymol blue, methyl orange and Bromocresol green under visible light (300-W Xe lamp; λ > 420 nm). The results show that the alloy of TiO 2 with 1 mol% of Mn 2O 3 (MNT1) exhibit photocatalytic activity 3-5 times higher than that of P25 TiO 2 for oxidation of various dyes (RB, TB, MO and BG). The average particle size and crystallite size of MNT1 were found to be 100 nm and 12 nm measured from SEM and XRD, respectively. The EPR spectra of the Mn 2O 3/TiO 2 samples is a sharp five-line Mn(III) component centered on geff = 1 .99.

  16. Oxazine laser dyes

    DOEpatents

    Hammond, Peter R.; Field, George F.

    1992-01-01

    New oxazine compounds useful as dye laser media in solution, are superiior to prior art materials. The oxazine dyes useful when pumped by the 578.2 nm copper line to operate in the 700-800 nm range are described by formula I ##STR1##

  17. Bi-anchoring organic sensitizers of type D-(π-A)2 comprising thiophene-2-acetonitrile as π-spacer and malonic acid as electron acceptor for dye sensitized solar cell applications

    NASA Astrophysics Data System (ADS)

    Reddy, Gachumale Saritha; Ramkumar, Sekar; Asiri, Abdullah M.; Anandan, Sambandam

    2015-06-01

    Two new bi-anchoring organic sensitizers of type D-(π-A)2 comprising the identical π-spacer (thiophene-2-acetonitrile) and electron acceptor (malonic acid) but different aryl amine as electron donors (diphenylamine and carbazole) were synthesized, characterized and fabricated metal free dye-sensitized solar cell devices. The intra molecular charge transfer property and electrochemical property of these dyes were investigated by molecular absorption, emission, cyclic voltammetric experiments and in addition, quantum chemical calculation studies were performed to provide sufficient driving force for the electron injection into the conduction band of TiO2 which leads to efficient charge collection. Among the fabricated devices, carbazole based device exhibits high current conversion efficiency (η = 4.7%) with a short circuit current density (JSC) 15.3 mA/cm2, an open circuit photo voltage (VOC) of 0.59 V and a fill factor of 0.44 under AM 1.5 illumination (85 mW/cm2) compared to diphenylamine based device.

  18. Low temperature (150 °C) fabrication of high-performance TiO{sub 2} films for dye-sensitized solar cells using ultraviolet light and plasma treatments of TiO{sub 2} paste containing organic binder

    SciTech Connect

    Zen, Shungo Ono, Ryo; Inoue, Yuki

    2015-03-14

    Dye-sensitized solar cells (DSSCs) require annealing of TiO{sub 2} photoelectrodes at 450 °C to 550 °C. However, such high-temperature annealing is unfavorable because it limits the use of materials that cannot withstand high temperatures, such as plastic substrates. In our previous paper, a low-temperature annealing technique of TiO{sub 2} photoelectrodes using ultraviolet light and dielectric barrier discharge treatments was proposed to reduce the annealing temperature from 450 °C to 150 °C for a TiO{sub 2} paste containing an organic binder. Here, we measure the electron diffusion length in the TiO{sub 2} film, the amount of dye adsorption on the TiO{sub 2} film, and the sheet resistance of a glass substrate of samples manufactured with the 150 °C annealing method, and we discuss the effect that the 150 °C annealing method has on those properties of DSSCs.

  19. Interactions of Enolizable Barbiturate Dyes.

    PubMed

    Schade, Alexander; Schreiter, Katja; Rüffer, Tobias; Lang, Heinrich; Spange, Stefan

    2016-04-11

    The specific barbituric acid dyes 1-n-butyl-5-(2,4-dinitro-phenyl) barbituric acid and 1-n-butyl-5-{4-[(1,3-dioxo-1H-inden-(3 H)-ylidene)methyl]phenyl}barbituric acid were used to study complex formation with nucleobase derivatives and related model compounds. The enol form of both compounds shows a strong bathochromic shift of the UV/Vis absorption band compared to the rarely coloured keto form. The keto-enol equilibria of the five studied dyes are strongly dependent on the properties of the environment as shown by solvatochromic studies in ionic liquids and a set of organic solvents. Enol form development of the barbituric acid dyes is also associated with alteration of the hydrogen bonding pattern from the ADA to the DDA type (A=hydrogen bond acceptor site, D=donor site). Receptor-induced altering of ADA towards DDA hydrogen bonding patterns of the chromophores are utilised to study supramolecular complex formation. As complementary receptors 9-ethyladenine, 1-n-butylcytosine, 1-n-butylthymine, 9-ethylguanidine and 2,6-diacetamidopiridine were used. The UV/Vis spectroscopic response of acid-base reaction compared to supramolecular complex formation is evaluated by (1)H NMR titration experiments and X-ray crystal structure analyses. An increased acidity of the barbituric acid derivative promotes genuine salt formation. In contrast, supramolecular complex formation is preferred for the weaker acidic barbituric acid. PMID:26945529

  20. Turn-on fluorescence triggered by selective internal dye replacement in MOFs.

    PubMed

    Wuttke, Stefan; Dietl, Christian; Hinterholzinger, Florian M; Hintz, Henrik; Langhals, Heinz; Bein, Thomas

    2014-04-01

    Coordinatively unsaturated metal sites (CUS) are used to create dye-functionalized metal-organic frameworks (MOFs). The quenching of dye fluorescence through interactions with the CUS can be utilised for chemical sensing of Lewis bases that displace the dye from the CUS, resulting in a triggered turn-on fluorescence signal.

  1. Genome sequence of Citrobacter sp. strain A1, a dye-degrading bacterium.

    PubMed

    Chan, Giek Far; Gan, Han Ming; Rashid, Noor Aini Abdul

    2012-10-01

    Citrobacter sp. strain A1, isolated from a sewage oxidation pond, is a facultative aerobe and mesophilic dye-degrading bacterium. This organism degrades azo dyes efficiently via azo reduction and desulfonation, followed by the successive biotransformation of dye intermediates under an aerobic environment. Here we report the draft genome sequence of Citrobacter sp. A1.

  2. Decolorization and removal of textile and non-textile dyes from polluted wastewater and dyeing effluent by using potato (Solanum tuberosum) soluble and immobilized polyphenol oxidase.

    PubMed

    Khan, Amjad Ali; Husain, Qayyum

    2007-03-01

    Celite bound potato polyphenol oxidase preparation was employed for the treatment of wastewater/dye effluent contaminated with reactive textile and non-textile dyes, Reactive Blue 4 and Reactive Orange 86. The maximum decolorization was found at pH 3.0 and 4.0 in case of Reactive Blue 4 and Reactive Orange 86, respectively. Immobilized potato polyphenol oxidase was significantly more effective in decolorizing the individual dye and complex mixtures of dyes as compared to soluble enzyme. The absorption spectra of the treated and untreated dye mixture and dyeing effluent exhibited a marked difference in the absorption value at various wavelengths. The polluted water contaminated with an individual dye or mixtures of dyes treated with soluble and immobilized potato polyphenol oxidase resulted in the remarkable loss in total organic carbon.

  3. Decolorization and removal of textile and non-textile dyes from polluted wastewater and dyeing effluent by using potato (Solanum tuberosum) soluble and immobilized polyphenol oxidase.

    PubMed

    Khan, Amjad Ali; Husain, Qayyum

    2007-03-01

    Celite bound potato polyphenol oxidase preparation was employed for the treatment of wastewater/dye effluent contaminated with reactive textile and non-textile dyes, Reactive Blue 4 and Reactive Orange 86. The maximum decolorization was found at pH 3.0 and 4.0 in case of Reactive Blue 4 and Reactive Orange 86, respectively. Immobilized potato polyphenol oxidase was significantly more effective in decolorizing the individual dye and complex mixtures of dyes as compared to soluble enzyme. The absorption spectra of the treated and untreated dye mixture and dyeing effluent exhibited a marked difference in the absorption value at various wavelengths. The polluted water contaminated with an individual dye or mixtures of dyes treated with soluble and immobilized potato polyphenol oxidase resulted in the remarkable loss in total organic carbon. PMID:16765044

  4. Photocatalytic degradation of organic dyes by La³⁺/Ce³⁺-H₃PW₁₂O₄₀ under different light irradiation.

    PubMed

    Li, Taohai; Li, Quanguo; Yan, Jing; Li, Feng

    2014-06-28

    New photocatalysts (La(3+)-H3PW12O40 and Ce(3+)-H3PW12O40) were prepared, and the degradation activity of these products was evaluated. These photocatalysts were synthesized by the hydrothermal method assisted by PEG-1000 from the reactions of LaCl3 or CeCl3 and phosphotungstic acid. The prepared catalysts were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), ultraviolet-visible diffuse reflection spectroscopy (UV-vis) and thermal gravimetric analysis (TGA). The catalytic activity of La(3+)-H3PW12O40 and Ce(3+)-H3PW12O40 was evaluated by adopting methyl orange (MO) and Rhodamine B (RhB) as model dyes, and the reaction was carried out under UV- and visible light irradiation.

  5. Dye system for dye laser applications

    SciTech Connect

    Hammond, P.R.

    1991-05-21

    This patent describes a dye of the DCM family, (2-methyl-6-(2-(1,2,3,4-tetrahydro-1-methyl-6-quinolinyl)ethenyl)-4H-pyran-4-ylidene)-propanedinitrile, dissolved in 2-phenoxyethanol, is non-mutagenic, stable and efficient, particularly in a pumped continuous wave laser system.

  6. Dye system for dye laser applications

    DOEpatents

    Hammond, Peter R.

    1991-01-01

    A dye of the DCM family, [2-methyl-6-[2-(1,2,3,4-tetrahydro-1-methyl-6-quinolinyl)ethenyl]-4H-pyran -4-ylidene]-propanedinitrile, dissolved in 2-phenoxyethanol, is non-mutagenic, stable and efficient, particularly in a pumped continuous wave laser system.

  7. Improvement of catalytic activity of Fe3O4/CuO/TiO2 nanocomposites using the combination of ultrasonic and UV light irradiation for degradation of organic dyes

    NASA Astrophysics Data System (ADS)

    Fauzian, Malleo; Taufik, Ardiansyah; Saleh, Rosari

    2016-04-01

    Iron-copper-titania mixed oxides was synthesized with Fe3O4/CuO to various TiO2 molar ratio using sol-gel method at low temperature and the intrinsic characteristics were studied by a variety of techniques such as X-ray diffraction (XRD), vibrating sample magnetometer (VSM) and BET surface area analyzer. The results demonstrate that all samples contained Fe3O4, CuO and TiO2 structures and exhibited ferromagnetic behavior at room temperature. In this study, methylene blue is used as a model of organic dyes. The degradation of methylene blue was observed using sonocatalysis and photocatalysis systems simultaneously. The experimental results showed that kinetic data followed the pseudo-first order model and the apparent rate constant of simultaneously processes of sonocatalysis and photocatalysis is higher than the respective individual processes.

  8. Matrix-assisted laser desorption/ionization mass spectrometric analysis of poly(3,4-ethylenedioxythiophene) in solid-state dye-sensitized solar cells: comparison of in situ photoelectrochemical polymerization in aqueous micellar and organic media.

    PubMed

    Zhang, Jinbao; Ellis, Hanna; Yang, Lei; Johansson, Erik M J; Boschloo, Gerrit; Vlachopoulos, Nick; Hagfeldt, Anders; Bergquist, Jonas; Shevchenko, Denys

    2015-04-01

    Solid-state dye-sensitized solar cells (sDSCs) are devoid of such issues as electrolyte evaporation or leakage and electrode corrosion, which are typical for traditional liquid electrolyte-based DSCs. Poly(3,4-ethylenedioxythiophene) (PEDOT) is one of the most popular and efficient p-type conducting polymers that are used in sDSCs as a solid-state hole-transporting material. The most convenient way to deposit this insoluble polymer into the dye-sensitized mesoporous working electrode is in situ photoelectrochemical polymerization. Apparently, the structure and the physicochemical properties of the generated conducting polymer, which determine the photovoltaic performance of the corresponding solar cell, can be significantly affected by the preparation conditions. Therefore, a simple and fast analytical method that can reveal information on polymer chain length, possible chemical modifications, and impurities is strongly required for the rapid development of efficient solar energy-converting devices. In this contribution, we applied matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) for the analysis of PEDOT directly on sDSCs. It was found that the PEDOT generated in aqueous micellar medium possesses relatively shorter polymeric chains than the PEDOT deposited from an organic medium. Furthermore, the micellar electrolyte promotes a transformation of one of the thiophene terminal units to thiophenone. The introduction of a carbonyl group into the PEDOT molecule impedes the growth of the polymer chain and reduces the conductivity of the final polymer film. Both the simplicity of sample preparation (only application of the organic matrix onto the solar cell is needed) and the rapidity of analysis hold the promise of making MALDI MS an essential tool for the physicochemical characterization of conducting polymer-based sDSCs.

  9. Green synthesis of the reduced graphene oxide-CuI quasi-shell-core nanocomposite: A highly efficient and stable solar-light-induced catalyst for organic dye degradation in water

    NASA Astrophysics Data System (ADS)

    Choi, Jiha; Reddy, D. Amaranatha; Islam, M. Jahurul; Seo, Bora; Joo, Sang Hoon; Kim, Tae Kyu

    2015-12-01

    Surfactant-free, reduced graphene oxide (RGO)-CuI quasi-shell-core nanocomposites were successfully synthesized using ultra-sonication assisted chemical method at room temperature. The morphologies, structures and optical properties of the CuI and CuI-RGO nanocomposites were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transformed infrared spectroscopy (FTIR), UV-visible absorption spectroscopy, and photoluminescence (PL) spectroscopy. Morphological and structural analyses indicated that the CuI-RGO core-shell nanocomposites comprise single-crystalline face-centered cubic phase CuI nanostructures, coated with a thin RGO quasi-shell. Photocatalysis experiments revealed that the as-synthesized CuI-RGO nanocomposites exhibit remarkably enhanced photocatalytic activities and stabilities for photo degradation of Rhodamine-B (RhB) organic dye under simulated solar light irradiation. The photo degradation ability is strongly affected by the concentration of RGO in the nanocomposites; the highest photodegradation rate was obtained at a graphene loading content of 2 mg mL-1 nanocomposite. The remarkable photocatalytic performance of the CuI-RGO nanocomposites mainly originates from their unique adsorption and electron-accepting and electron-transporting properties of RGO. The present work provides a novel green synthetic route to producing CuI-RGO nanocomposites without toxic solvents or reducing agents, thereby providing highly efficient and stable solar light-induced RGO-CuI quasi-shell-core nanocomposites for organic dye photo degradation in water.

  10. Influence of Exposure to Imidacloprid on Survivorship, Reproduction and Vitellin Content of the Carmine Spider Mite, Tetranychus cinnabarinus

    PubMed Central

    Zeng, Chun-Xiang; Wang, Jin-Jun

    2010-01-01

    Occasional reports linking neonicotinoid insecticide applications to field population outbreaks of the spider mite have been a topic of concern for integrated pest management programs. To elucidate the impacts of a neonicotinoid insecticide on the carmine spider mite, Tetranychus cinnabarinus Boisduval (Acari: Tetranychidae), the survivorship, reproduction, and vitellin contents of the mite were investigated after exposure to various concentrations of imidacloprid on the V. unguiculata leaf discs at 25°C, 80% RH and a photoperiod of 14:10 (L:D) in the laboratory. The results showed that the field-relevant dose of imidacloprid did not significantly affect the hatch rate of eggs or pre-imaginal survivorship of the mite, while sublethal doses of imidacloprid, previously determined for Myzus persicae, led to a significant increase in the hatch rate of eggs and pre-imaginal survivorship of the mite compared to the untreated control. Adult longevity and fecundity of T. cinnabarinus for imidacloprid-treated populations were slightly prolonged and increased, respectively, but the difference from the untreated control was not significant. The vitellin content in eggs increased significantly after exposure to imidacloprid. Imidacloprid may be one of the major reasons for the outbreak of T. cinnabarinus in the field. PMID:20578884

  11. Application of video recording technology to improve husbandry and reproduction in the carmine bee-eater (Merops n. nubicus).

    PubMed

    Ferrie, Gina M; Sky, Christy; Schutz, Paul J; Quinones, Glorieli; Breeding, Shawnlei; Plasse, Chelle; Leighty, Katherine A; Bettinger, Tammie L

    2016-01-01

    Incorporating technology with research is becoming increasingly important to enhance animal welfare in zoological settings. Video technology is used in the management of avian populations to facilitate efficient information collection on aspects of avian reproduction that are impractical or impossible to obtain through direct observation. Disney's Animal Kingdom(®) maintains a successful breeding colony of Northern carmine bee-eaters. This African species is a cavity nester, making their nesting behavior difficult to study and manage in an ex situ setting. After initial research focused on developing a suitable nesting environment, our goal was to continue developing methods to improve reproductive success and increase likelihood of chicks fledging. We installed infrared bullet cameras in five nest boxes and connected them to a digital video recording system, with data recorded continuously through the breeding season. We then scored and summarized nesting behaviors. Using remote video methods of observation provided much insight into the behavior of the birds in the colony's nest boxes. We observed aggression between birds during the egg-laying period, and therefore immediately removed all of the eggs for artificial incubation which completely eliminated egg breakage. We also used observations of adult feeding behavior to refine chick hand-rearing diet and practices. Although many video recording configurations have been summarized and evaluated in various reviews, we found success with the digital video recorder and infrared cameras described here. Applying emerging technologies to cavity nesting avian species is a necessary addition to improving management in and sustainability of zoo avian populations.

  12. Application of video recording technology to improve husbandry and reproduction in the carmine bee-eater (Merops n. nubicus).

    PubMed

    Ferrie, Gina M; Sky, Christy; Schutz, Paul J; Quinones, Glorieli; Breeding, Shawnlei; Plasse, Chelle; Leighty, Katherine A; Bettinger, Tammie L

    2016-01-01

    Incorporating technology with research is becoming increasingly important to enhance animal welfare in zoological settings. Video technology is used in the management of avian populations to facilitate efficient information collection on aspects of avian reproduction that are impractical or impossible to obtain through direct observation. Disney's Animal Kingdom(®) maintains a successful breeding colony of Northern carmine bee-eaters. This African species is a cavity nester, making their nesting behavior difficult to study and manage in an ex situ setting. After initial research focused on developing a suitable nesting environment, our goal was to continue developing methods to improve reproductive success and increase likelihood of chicks fledging. We installed infrared bullet cameras in five nest boxes and connected them to a digital video recording system, with data recorded continuously through the breeding season. We then scored and summarized nesting behaviors. Using remote video methods of observation provided much insight into the behavior of the birds in the colony's nest boxes. We observed aggression between birds during the egg-laying period, and therefore immediately removed all of the eggs for artificial incubation which completely eliminated egg breakage. We also used observations of adult feeding behavior to refine chick hand-rearing diet and practices. Although many video recording configurations have been summarized and evaluated in various reviews, we found success with the digital video recorder and infrared cameras described here. Applying emerging technologies to cavity nesting avian species is a necessary addition to improving management in and sustainability of zoo avian populations. PMID:26661620

  13. Dyeing of Polyester with Disperse Dyes: Part 2. Synthesis and Dyeing Characteristics of Some Azo Disperse Dyes for Polyester Fabrics.

    PubMed

    Al-Etaibi, Alya M; Alnassar, Huda S; El-Apasery, Morsy Ahmed

    2016-01-01

    The goal of this study was to utilize carrier for accelerating the rate of dyeing not only to enhance dyeing of polyester fabrics dyed with disperse dyes 3a,b, but also to save energy. Both the color strength expressed as dye uptake and the fastness properties of the dyed fabrics were evaluated. PMID:27367659

  14. Diode-pumped dye laser

    NASA Astrophysics Data System (ADS)

    Burdukova, O. A.; Gorbunkov, M. V.; Petukhov, V. A.; Semenov, M. A.

    2016-10-01

    This letter reports diode pumping for dye lasers. We offer a pulsed dye laser with an astigmatism-compensated three-mirror cavity and side pumping by blue laser diodes with 200 ns pulse duration. Eight dyes were tested. Four dyes provided a slope efficiency of more than 10% and the highest slope efficiency (18%) was obtained for laser dye Coumarin 540A in benzyl alcohol.

  15. Quirks of dye nomenclature. 3. Trypan blue.

    PubMed

    Cooksey, C J

    2014-11-01

    Trypan blue is colorant from the 19(th) century that has an association with Africa as a chemotherapeutic agent against protozoan (Trypanosomal) infections, which cause sleeping sickness. The dye still is used for staining biopsies, living cells and organisms, and it also has been used as a colorant for textiles.

  16. Solar light induced degradation of reactive dye using photocatalysis.

    PubMed

    Park, Jae-Hong; Cho, Il-Hyoung; Kim, Young-Gyu

    2004-01-01

    Outdoors experiment with natural solar light instead of using artificial UV light was also conducted to investigate alternative energy source applicability on organics degradation. The results of this study were as follows. Degradation of the reactive dye, Red 120, with TiO2/solar light was enhanced by augmentation in TiO2 loading, and UV light intensity but was inhibited by increase in initial dye concentration. With both solar light illumination and TiO2 present, reactive dye was more effectively eliminated than with either solar light or TiO, alone. Photocatalytic removal efficiency of reactive dye increased with increasing TiO2 dosage. However, over 1.5 gL(-1) of TiO2 dosage, the efficiency reached a plateau. The degradation rate of reactive dye, Red 120, was strongly dependent on initial dye concentration, and all the experimental data were fit to the first-order rate equation. Photocatalytic degradation of reactive dye increased linearly with increasing UV light intensity. It is found that the presence of thick clouds in the sky markedly increased the time required for degradation of reactive dye. On the basis of these experimental observations, the photo-oxidation degradation of reactive dye using TiO2 under solar light irradiation can be feasible application of the advanced oxidation process.

  17. Hair dye poisoning

    MedlinePlus

    ... are: Arsenic Bismuth Denatured alcohol Lead ( lead poisoning ) Mercury Pyrogallol Silver Hair dyes may contain other harmful ... bleeding and infection. Continued exposure to lead or mercury can lead to permanent brain and nervous system ...

  18. New synthetic routes towards soluble and dissymmetric triphenodioxazine dyes designed for dye-sensitized solar cells.

    PubMed

    Nicolas, Yohann; Allama, Fouzia; Lepeltier, Marc; Massin, Julien; Castet, Frédéric; Ducasse, Laurent; Hirsch, Lionel; Boubegtiten, Zahia; Jonusauskas, Gediminas; Olivier, Céline; Toupance, Thierry

    2014-03-24

    New π-conjugated structures are constantly the subject of research in dyes and pigments industry and electronic organic field. In this context, the triphenodioxazine (TPDO) core has often been used as efficient photostable pigments and once integrated in air stable n-type organic field-effect transistor (OFET). However, little attention has been paid to the TPDO core as soluble materials for optoelectronic devices, possibly due to the harsh synthetic conditions and the insolubility of many compounds. To benefit from the photostability of TPDO in dye-sensitized solar cells (DSCs), an original synthetic pathway has been established to provide soluble and dissymmetric molecules applied to a suitable design for the sensitizers of DSC. The study has been pursued by the theoretical modeling of opto-electronic properties, the optical and electronic characterizations of dyes and elaboration of efficient devices. The discovery of new synthetic pathways opens the way to innovative designs of TPDO for materials used in organic electronics.

  19. DFT study of the effect of different metals on structures and electronic spectra of some organic-metal compounds as sensitizing dyes

    NASA Astrophysics Data System (ADS)

    Tang, Guodong; Li, Rongqing; Kou, Shanshan; Tang, Tingling; Zhang, Yu; Wang, Yiwei

    2014-02-01

    Ruthenium polypyridined-derivative complexes are used in dye-sensitized solar cell [DSSC] as a light to current conversion sensitizer. In order to lower the cost of the DSSC the normal transition metals were used to replace the noble metal ruthenium, and some compounds [ML2L'] (M = Pt, Fe, Ni, Zn; L = isonicotinic acid, L' = maleonitriledithiolate, I = PtL2L', II = FeL2L', III = NiL2L', IV = ZnL2L') were selected as the replacement. The geometries, electronic structures and optical absorption spectra of these compounds have been studied by using density functional theory (DFT) calculation at the B3LYP/LANL2DZ, B3P86/LANL2DZ, B3LYP/GEN level of theory. All the geometric parameters are close to the experimental values. The HOMOs are mainly on the maleonitriledithiolate groups mixed with fewer characters of the metal atom, the LUMOs are mainly on the two pyridine ligands. This means that the electron transition is attributed to the LLCT. The maximum absorptions of complexes are found to be at 351 nm, 806 nm for compound I, and 542 nm for compound II. The maximum absorptions of complexes are found to be at 884 nm for compound III, and 560 nm for compound IV. This means that those compounds may be as a suitable sensitizer for solar energy conversion applications.

  20. Facile water-stability evaluation of metal-organic frameworks and the property of selective removal of dyes from aqueous solution.

    PubMed

    Qi, Zhao-Peng; Yang, Ji-Min; Kang, Yan-Shang; Guo, Fan; Sun, Wei-Yin

    2016-06-01

    A facile and universal method was developed to evaluate the relative water stability of porous MOFs and morphological evolution was achieved by controlling the volume ratio of DMF and H2O. The relative water stability of the studied MOFs is in the order HKUST-1 > MOF-505 ∼ UMCM-150 > NOTT-101 > DUT-23(Cu) > [Zn2(BPnDC)2(DABCO)] ∼ [Cu3(TPTrC)2(DABCO)] > MOF-5. In addition, DUT-23(Cu) [Cu6(BTB)4(BPY)3] (H3BTB = 4,4',4''-benzene-1,3,5-triyl-tribenzoic acid, BPY = 4,4'-bipyridine) nanoparticles obtained with a volume ratio of DMF and H2O of 18 : 2 show excellent adsorption capacity for methylene blue (MB) (814 mg g(-1)) with high selectivity compared with methyl orange, rhodamine B, and acid chrome blue K dyes due to the size and the electrostatic repulsion effects in aqueous solution. PMID:27139895