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Sample records for azo dye polymer

  1. Anaerobic azo dye reduction

    OpenAIRE

    Zee, van der, F.P.

    2002-01-01

    Azo dyes, aromatic moieties linked together by azo (-N=N-) chromophores, represent the largest class of dyes used in textile-processing and other industries. The release of these compounds into the environment is undesirable, not only because of their colour, but also because many azo dyes and their breakdown products are toxic and/or mutagenic to life. To remove azo dyes from wastewater, a biological treatment strategy based on anaerobic reduction of the azo dye...

  2. Radiolysis of organic triphenylmethane, anthraquinone, xanthene, oxazine, thiazine, and azo dyes in polymers films

    International Nuclear Information System (INIS)

    Khabarov, V.N.; Kozlov, L.L.; Molin, A.A.; Mekhanik, T.V.

    1989-01-01

    The effect of the oxygen in the air and the temperature on radiochemical processes of decolorization of triphenylmethane, anthraquinone, xanthene, oxazine, thiazine, and azo dyes in polymer matrices of different chemical natures was studied. The rate of radiation decolorization for most of the dyes increases in irradiation in the presence of O 2 , which is hypothetically due to oxidation of the dye by singlet oxygen. The organic dyes exhibit the highest radiation stability in polyethylene terephthalate and polystyrene films

  3. Anaerobic azo dye reduction

    NARCIS (Netherlands)

    Zee, van der F.P.

    2002-01-01

    Azo dyes, aromatic moieties linked together by azo (-N=N-) chromophores, represent the largest class of dyes used in textile-processing and other industries. The release of these compounds into the environment is undesirable, not only because of their colour, but also

  4. Removal of anionic azo dyes from aqueous solution by functional ionic liquid cross-linked polymer

    International Nuclear Information System (INIS)

    Gao, Hejun; Kan, Taotao; Zhao, Siyuan; Qian, Yixia; Cheng, Xiyuan; Wu, Wenli; Wang, Xiaodong; Zheng, Liqiang

    2013-01-01

    Highlights: • Equilibrium, kinetic and thermodynamic of adsorption of dyes onto PDVB-IL was investigated. • PDVB-IL has a high adsorption capacity to treat dyes solution. • Higher adsorption capacity is due to the functional groups of PDVB-IL. • Molecular structure of dyes influences the adsorption capacity. -- Abstract: A novel functional ionic liquid based cross-linked polymer (PDVB-IL) was synthesized from 1-aminoethyl-3-vinylimidazolium chloride and divinylbenzene for use as an adsorbent. The physicochemical properties of PDVB-IL were investigated by Fourier transform infrared spectroscopy, scanning electron microscopy and thermogravimetric analysis. The adsorptive capacity was investigated using anionic azo dyes of orange II, sunset yellow FCF, and amaranth as adsorbates. The maximum adsorption capacity could reach 925.09, 734.62, and 547.17 mg/g for orange II, sunset yellow FCF and amaranth at 25 °C, respectively, which are much better than most of the other adsorbents reported earlier. The effect of pH value was investigated in the range of 1–8. The result shows that a low pH value is found to favor the adsorption of those anionic azo dyes. The adsorption kinetics and isotherms are well fitted by a pseudo second-order model and Langmuir model, respectively. The adsorption process is found to be dominated by physisorption. The introduction of functional ionic liquid moieties into cross-linked poly(divinylbenzene) polymer constitutes a new and efficient kind of adsorbent

  5. Photo refractive effect in an Azo-dye doped polymer

    International Nuclear Information System (INIS)

    Khoshsima, H.

    1997-01-01

    Photo refractive, todays, is the frontier of nonlinear optics. The higher nonlinear properties, the more photo refractive effect will appear. In this experimental study, applying the experimental arrangement for Degenerate Four Wave Minx ing, we got benefit of P.V.K base polymer made complex with T.N.F, that is basically charge carrier. D.M.N.P.A.A chromophore molecules are used to produce second order nonlinear optics effect. Under the best experimental condition, the measured diffraction efficiency was about 70%

  6. Linearly and circularly polarized laser photoinduced molecular order in azo dye doped polymer films

    Directory of Open Access Journals (Sweden)

    Saad Bendaoud

    2017-01-01

    Full Text Available Photo-induced behavior of Azo Disperse one (AZD1 doped Poly(Methyl MethAcrylate (PMMA using both linear and circular polarized light is studied. The anisotropy is not erased by the circular polarization light. The circular polarization light combined with relatively long lifetime of the cis state in azo dye doped polymers activate all transverse directions of the angular hole burning through the spot in the film inducing anisotropy. Under circular polarized light, there is no orientation perpendicularly to the helex described by the rotating electric field vector, trans molecules reorients in the propagation direction of the pump beam. The polarization state of the probe beam after propagation through the pumped spot depends strongly on the angle of incidence of both pump and probe beams on the input face. In the case where circular polarized pump and probe beams are under the same angle of incidence, the probe beam “sees” anisotropic film as if it is isotropic. Results of this work shows the possibility to reorient azobenzene-type molecules in two orthogonal directions using alternately linearly and circularly polarized beams.

  7. Synthesis and optical properties of azo -dye-attached novel second-order NLO polymers with high thermal stability

    Science.gov (United States)

    Ushiwata, Takami; Okamoto, Etsuya; Komatsu, Kyoji; Kaino, Toshikuni

    2001-06-01

    Novel second order nonlinear optical (NLO) polymethacrylate or polyacrylate polymers with high glass transition temperatures containing an azo dye attached as side-chain have been prepared using a new approach from polymethacrylic acid or polyacrylic acid as starting materials. Glass transition temperatures of 150 approximately 170 degree Celsius were obtained for Disperse red 1 dye attached polymethacrylic acid. These are attributed to the hydrogen bonding between the residual carboxyl groups in the starting polymers. Poled films by corona poling exhibited large NLO susceptibilities, (chi) (2)33 up to 53 pm/V at a wavelength of 1.3 micrometer. Due to the high glass transition temperatures of the polymers, long-term stability of the optical nonlinearity at 100 degrees Celsius was observed for 200 hrs or more. However residual carboxyl groups caused absorbance decrease mainly by hydrolysis of the ester bonds of the polymers investigated by UV-Vis absorption measurement. The stability of induced polar order of the NLO polymer was enhanced by using aminoalkyl chromophore and imidizing it thermally to introduce imide structure into the polymer main-chain. This imidized polymer exhibited (chi) (2)33 of 45 pm/V at a wavelength of 1.3 micrometer and maintained about 90% of the initial value after 230 hrs or more at 100 degrees Celsius.

  8. Synthesis of azo pyridone dyes

    Directory of Open Access Journals (Sweden)

    Mijin Dušan Ž.

    2011-01-01

    Full Text Available Over 50% of all colorants which are used nowdays are azo dyes and pigments, and among them arylazo pyridone dyes (and pigments have became of interest in last several decades due to the high molar extinction coefficient, and the medium to high light and wet fastness properties. They find application generally as disperse dyes. The importance of disperse dyes increased in the 1970s and 1980s due to the use of polyester and nylon as the main synthetic fibers. Also, disperse dyes were used rapidly since 1970 in inks for the heat-transfer printing of polyester. The main synthetic route for the preparation of azo dyes is coupling reaction between an aromatic diazo compound and a coupling component. Of all dyes manufactured, about 60% are produced by this reaction. Arylazo pyridone dyes can be prepared from pyridone moiety as a coupling component, where substituent can be on nitrogen, and diazonim salts which can be derived from different substituted anilines or other heterocyclic derivatives. In addition, arylazo dyes containing pyridone ring can be prepared from arylazo diketones or arylazo ketoesters (obtained by coupling β-diketones or β-ketoesters with diazonim salts by condensation with cyanoacetamide. Disazo dyes can be prepared by tetrazotizing a dianiline and coupling it with a pyridone or by diazotizing aniline and coupling it with a dipyridone. Trisazo dyes can be also prepared by diazotizing of aniline and coupling it with a tripyridone or by hexazotizing a trianiline and coupling it with a pyridone. The main goal of this paper is to give a brief review on the synthesis of arylazo pyridone dyes due to the lack of such reviews. In addition, some properties of arylazo pyridone dyes as light fastness and azo-hydrazon tautomerism are disccused.

  9. Aerobic decolourization of two reactive azo dyes under varying ...

    African Journals Online (AJOL)

    STORAGESEVER

    2010-02-01

    Feb 1, 2010 ... Azo dyes generally resist aerobic microbial degra- dation, only organisms with specialized azo dye reducing enzymes were found to degrade azo dyes under fully aerobic ... textile mill, in sterile plastic bottles. Isolation of ...

  10. Enhancement of the optical response in a biodegradable polymer/azo-dye film by the addition of carbon nanotubes

    International Nuclear Information System (INIS)

    Costanzo, Guadalupe Díaz; Ledesma, Silvia; Ribba, Laura; Goyanes, Silvia

    2014-01-01

    A new biodegradable photoresponsive material was developed using poly(lactic acid) (PLA) as the matrix material and Disperse Orange 3 (DO3) as photoisomerizable azo-dye. It was observed that the addition of multi-walled carbon nanotubes (MWCNTs) leads to a new phenomenon consisting of an enhancement of the optical anisotropy in a wide range of temperatures. In particular, the optical anisotropy increases 100% at room temperature. Moreover, the material containing MWCNTs shows a faster optical response that is evidenced as an increase in the growth rate of optical anisotropy. Spectroscopic data is provided to study the interaction among DO3, MWCNTs and PLA. The enhancement of optical anisotropy obtained with the addition of MWCNTs was related to the glass transition temperature (T g ) of each material. Maximum optical anisotropy was obtained 15 °C below the T g for both materials. Results are interpreted in terms of the interactions among DO3, MWCNTs and PLA and the packing density of the dye into the polymer chains. (paper)

  11. Biological wastewater treatment of azo dyes

    Energy Technology Data Exchange (ETDEWEB)

    Shaul, G.M.; Dempsey, C.R.; Dostal, K.A. (Environmental Protection Agency, Cincinnati, OH (USA))

    1988-09-01

    EPA Water Engineering Research Laboratory, Office of Research and Development, undertook a study to determine the fate of specific water soluble azo dye compounds in the activated sludge process (ASP). The study was approached by dosing the feed to the pilot ASP systems with various water soluble azo dyes and by monitoring each dye compound through the system, analyzing both liquid and sludge samples. The fate of the parent dye compound was assessed via mass balance calculations. These data could determine if the compound was removed by adsorption, apparent biodegradation, or not removed at all. The paper presents results for 18 dye compounds tested from June 1985 through August 1987. The study was conducted at EPAs Test and Evaluation Facility in Cincinnati, Ohio. The objective of this study was to determine the partitioning of water soluble azo dyes in the ASP.

  12. Nano-Sized Zero Valent Iron and Covalent Organic Polymer Composites for Azo Dye Remediation

    DEFF Research Database (Denmark)

    Mines, Paul D.; Byun, Jeehye; Hwang, Yuhoon

    2014-01-01

    . In this study, the effect of various covalent organic polymers (COPs) as effective supporting materials for nZVI for optimal pollutant degradation was assessed. These COPs demonstrate promising results for the ability to adsorb and remove carbon dioxide, yielding the notion that they are capable of groundwater...... in chlorinated organics, heavy metals, and various other groundwater contaminants....

  13. Integrated and sequential anaerobic/aerobic biodegradation of azo dyes

    NARCIS (Netherlands)

    Tan, N.G.C.

    2001-01-01

    Azo dyes constitute a major class of environmental pollutants accounting for 60 to 70% of all dyes and pigments used. These compounds are characterized by aromatic moieties linked together with azo groups (-N=N-). The release of azo dyes into the environment is a concern due to coloration

  14. Degradation of azo dyes by environmental microorganisms and helminths

    Energy Technology Data Exchange (ETDEWEB)

    Kingthom Chung; Stevens, S.E. Jr. (Memphis State Univ., TN (United States). Dept. of Biology)

    1993-11-01

    The degradation of azo dyes by environmental microorganisms, fungi, and helminths is reviewed. Azo dyes are used in a wide variety of products and can be found in the effluent of most sewage treatment facilities. Substantial quantities of these dyes have been deposited in the environment, particularly in streams and rivers. Azo dyes were shown to affect microbial activities and microbial population sizes in the sediments and in the water columns of aquatic habitats. Only a few aerobic bacteria have been found to reduce azo dyes under aerobic conditions, and little is known about the process. A substantial number of anaerobic bacteria capable of azo dye reduction have been reported. The enzyme responsible for azo dye reduction has been partially purified, and characterization of the enzyme is proceeding. The nematode Ascaris lumbricoides and the cestode Moniezia expanza have been reported to reduce azo dyes anaerobically. Recently the fungus Phanerochaete chrysoporium was reported to mineralize azo dyes via a peroxidation-mediated pathway. A possible degradation pathway for the mineralization of azo dye is proposed and future research needs are discussed.

  15. The Orange Side of Disperse Red 1: Humidity-Driven Color Switching in Supramolecular Azo-Polymer Materials Based on Reversible Dye Aggregation.

    Science.gov (United States)

    Schoelch, Simon; Vapaavuori, Jaana; Rollet, Frédéric-Guillaume; Barrett, Christopher J

    2017-01-01

    Humidity detection, and the quest for low-cost facile humidity-sensitive indicator materials is of great interest for many fields, including semi-conductor processing, food transport and storage, and pharmaceuticals. Ideal humidity-detection materials for a these applications might be based on simple clear optical readout with no power supply, i.e.: a clear color change observed by the naked eye of any untrained observer, since it doesn't require any extra instrumentation or interpretation. Here, the introduction of a synthesis-free one-step procedure, based on physical mixing of easily available commercial materials, for producing a humidity memory material which can be easily painted onto a wide variety of surfaces and undergoes a remarkable color change (approximately 100 nm blue-shift of λ MAX ) upon exposure to various thresholds of levels of ambient humidity is reported. This strong color change, easily visible to as a red-to-orange color switch, is locked in until inspection, but can then be restored reversibly if desired, after moderate heating. By taking advantage of spontaneously-forming reversible 'soft' supramolecular bonds between a red-colored azo dye and a host polymer matrix, a reversible dye 'migration' aggregation appearing orange, and dis-aggregation back to red can be achieved, to function as the sensor. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. The UV and Laser Aging for PMMA/BDK/Azo-dye Polymer Blend Cured by UV Light Beams

    International Nuclear Information System (INIS)

    Ahmad, A A; Omari, A M

    2015-01-01

    A polymeric-based solution blend composed of Azo-dye methyl red (MR) doped with polymethelmethacrelate (PMMA) solution, in addition, to the BenzylDimethylKetal (BDK) photoinitiator was made with optimum molar ratios and deposited on glass substrate by spin coating technique. The samples were then exposed to UV light beams in order to assist the layers polymerization by the proper exposure process. The photo chemical reaction occurred during the UV light polymerization process induces photo refractive changes which were presented as a function of wavelength or photon energy. Two main strong absorption peaks were observed in the films at around 330 nm (3.75 eV) and 500 nm (2.48 eV) for different curing time periods. This phenomenon enhances the films usage for optical data storage media at these two wavelengths. Since the deposited films were then useful as based layers for Read/Write optical data storage media, they were then tested by UV or laser Read/Write beams independently. The optical properties of the films were investigated while exposed to each beam. Finally, their optical properties were investigated as a function of aging time in order to relate the temporary and/or permanent light-exposure effect on the films compared to their optical properties before the light exposure. The films show a low absorbance at 630 nm (1.97 eV) and high absorbance at 480 nm (2.58 eV). This fact makes it possible to record holographic gratings in the polymeric film upon light exposure. In all cases the optical properties were evaluated by using the very sensitive, non destructive surface testing spectroscopic ellipsometry technique. The films were characterized in the spectral range of 300 to 1000 nm using Lorentz oscillator model with one oscillator centred at 4.15 eV. This study has been supported by the SEM and EDAX results to investigate the effect of the UV and visible beams on their optical properties. The results of this research determined the proper conditions for

  17. Studies on Dyeing Performance of Novel Acid Azo Dyes and Mordent Acid Azo Dyes Based on 2,4-Dihydroxybenzophenone

    Directory of Open Access Journals (Sweden)

    Bharat C. Dixit

    2009-01-01

    Full Text Available Novel acid azo and mordent acid azo dyes have been prepared by the coupling of diazo solution of different aminonaphthol sulphonic acids and aromatic amino acids with 2,4-dihydroxybenzophenone. The resultant dyes were characterized by elemental analysis as well as IR and 1H NMR spectral studies. The UV-visible spectral data have also been discussed in terms of structure property relationship. The dyeing assessments of all the dyes were evaluated on wool and silk textile fibers. The dyeing of chrome pretreated wool and silk have also been monitored. The result shows that better hue was obtained on mordented fiber. Results of bactericidal studies of chrome pretreated fibers revealed that the toxicity of mordented dyes against bacteria is fairly good. Dyeing on wool and silk fibers resulted in yellowish pink to reddish brown colourations having excellent light fastness and washing fastness.

  18. Effects of reduction products of ortho-hydroxyl substituted azo dyes on biodecolorization of azo dyes

    Energy Technology Data Exchange (ETDEWEB)

    Liu Guangfei [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China); Wang Jing, E-mail: wangjingbio@yahoo.cn [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China); Lu Hong; Jin Ruofei; Zhou Jiti; Zhang Long [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental and Biological Science and Technology, Dalian University of Technology, Linggong Road No. 2, Dalian 116024 (China)

    2009-11-15

    The mediated effects of reduction products of some ortho-hydroxyl substituted azo dyes on biodecolorization were investigated. The results indicated that the addition of reduction products could effectively accelerate dye decolorization by Shigella sp. QRZ-1. The best accelerating effect was obtained with the addition of reduction products of Acid Red 14 (AR14), resulting in an over 3-fold increase in decolorization efficiency of many azo dyes. In sequencing batch reactor experiments, the accelerating effect of reduction products of AR14 was more obvious (1.5-fold) during the startup of the system. When the dye concentration was increased to 500 mg L{sup -1}, the accelerated decolorization efficiency was still maintained around 95%. The presence of AR14 in the feed enhanced the decolorization performance of anaerobic sludge, indicating that the strategy may be beneficial for practical application. 1-Naphthol-2-amino-4-sulfonic acid, which is one of the reduction products of AR14, may function as redox mediator to speed up azo dye biodecolorization.

  19. Effects of reduction products of ortho-hydroxyl substituted azo dyes on biodecolorization of azo dyes

    International Nuclear Information System (INIS)

    Liu Guangfei; Wang Jing; Lu Hong; Jin Ruofei; Zhou Jiti; Zhang Long

    2009-01-01

    The mediated effects of reduction products of some ortho-hydroxyl substituted azo dyes on biodecolorization were investigated. The results indicated that the addition of reduction products could effectively accelerate dye decolorization by Shigella sp. QRZ-1. The best accelerating effect was obtained with the addition of reduction products of Acid Red 14 (AR14), resulting in an over 3-fold increase in decolorization efficiency of many azo dyes. In sequencing batch reactor experiments, the accelerating effect of reduction products of AR14 was more obvious (1.5-fold) during the startup of the system. When the dye concentration was increased to 500 mg L -1 , the accelerated decolorization efficiency was still maintained around 95%. The presence of AR14 in the feed enhanced the decolorization performance of anaerobic sludge, indicating that the strategy may be beneficial for practical application. 1-Naphthol-2-amino-4-sulfonic acid, which is one of the reduction products of AR14, may function as redox mediator to speed up azo dye biodecolorization.

  20. Dielectric Properties of Azo Polymers: Effect of the Push-Pull Azo Chromophores

    Directory of Open Access Journals (Sweden)

    Xuan Zhang

    2018-01-01

    Full Text Available The relationship between the structure and the dielectric properties of the azo polymers was studied. Four azo polymers were synthesized through the azo-coupling reaction between the same precursor (PAZ and diazonium salts of 4-aminobenzoic acid ethyl ester, 4-aminobenzonitrile, 4-nitroaniline, and 2-amino-5-nitrothiazole, respectively. The precursor and azo polymers were characterized by 1H NMR, FT-IR, UV-vis, GPC, and DSC. The dielectric constant and dielectric loss of the samples were measured in the frequency range of 100 Hz–200 kHz. Due to the existence of the azo chromophores, the dielectric constant of the azo polymers increases compared with that of the precursor. In addition, the dielectric constant of the azo polymers increases with the increase of the polarity of the azo chromophores. A random copolymer (PAZ-NT-PAZ composed of the azo polymer PAZ-NT and the precursor PAZ was also prepared to investigate the content of the azo chromophores on the dielectric properties of the azo polymers. It showed that the dielectric constant increases with the increase of the azo chromophores. The results show that the dielectric constant of this kind of azo polymers can be controlled by changing the structures and contents of azo chromophores during the preparation process.

  1. Effect of dye structure and redox mediators on anaerobic azo and anthraquinone dye reduction

    Directory of Open Access Journals (Sweden)

    Mayara Carantino Costa

    2012-01-01

    Full Text Available We investigated the biological decolourisation of dyes with different molecular structures. The kinetic constant values (k1 achieved with azo dye Reactive Red 120 were 7.6 and 10.1 times higher in the presence of RM (redox mediators AQDS and riboflavin, respectively, than the assays lacking RM. The kinetic constant achieved with the azo dye Congo Red was 42 times higher than that obtained with the anthraquinone dye Reactive Blue 4. The effect of RM on dye reduction was more evident for azo dyes resistant to reductive processes, and ineffective for anthraquinone dyes because of the structural stability of the latter.

  2. Azo dye decolorization assisted by chemical and biogenic sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Prato-Garcia, Dorian [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico); Cervantes, Francisco J. [División de Ciencias Ambientales, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa de San José 2055, San Luis Potosí 78216 (Mexico); Buitrón, Germán, E-mail: gbuitronm@ii.unam.mx [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico)

    2013-04-15

    Highlights: ► Azo dyes were reduced efficiently by chemical and biogenic sulfide. ► Biogenic sulfide was more efficient than chemical sulfide. ► There was no competition between dyes and sulfate for reducing equivalents. ► Aromatic amines barely affected the sulfate-reducing process. -- Abstract: The effectiveness of chemical and biogenic sulfide in decolorizing three sulfonated azo dyes and the robustness of a sulfate-reducing process for simultaneous decolorization and sulfate removal were evaluated. The results demonstrated that decolorization of azo dyes assisted by chemical sulfide and anthraquinone-2,6-disulfonate (AQDS) was effective. In the absence of AQDS, biogenic sulfide was more efficient than chemical sulfide for decolorizing the azo dyes. The performance of sulfate-reducing bacteria in attached-growth sequencing batch reactors suggested the absence of competition between the studied azo dyes and the sulfate-reducing process for the reducing equivalents. Additionally, the presence of chemical reduction by-products had an almost negligible effect on the sulfate removal rate, which was nearly constant (94%) after azo dye injection.

  3. Modification of azo dyes by lactic acid bacteria.

    Science.gov (United States)

    Pérez-Díaz, I M; McFeeters, R F

    2009-08-01

    The ability of Lactobacillus casei and Lactobacillus paracasei to modify the azo dye, tartrazine, was recently documented as the result of the investigation on red coloured spoilage in acidified cucumbers. Fourteen other lactic acid bacteria (LAB) were screened for their capability to modify the food colouring tartrazine and other azo dyes of relevance for the textile industry. Most LAB modified tartrazine under anaerobic conditions, but not under aerobic conditions in modified chemically defined media. Microbial growth was not affected by the presence of the azo dyes in the culture medium. The product of the tartrazine modification by LAB was identified as a molecule 111 daltons larger than its precursor by liquid chromatography-mass spectrometry. This product had a purple colour under aerobic conditions and was colourless under anaerobic conditions. It absorbed light at 361 and 553 nm. LAB are capable of anabolizing azo dyes only under anaerobic conditions. IMPACT AND SIGNIFICANCE OF THE STUDY: Although micro-organisms capable of reducing the azo bond on multiple dyes have been known for decades, this is the first report of anabolism of azo dyes by food related micro-organisms, such as LAB.

  4. Aerobic decolourization of two reactive azo dyes under varying ...

    African Journals Online (AJOL)

    Bacillus cereus isolated from dye industrial waste, that is, effluent and soil samples was screened for its ability to decolourize two reactive azo dye – cibacron black PSG and cibacron red P4B under aerobic conditions at pH 7 and incubated at 35°C over a five day period. Different carbon and nitrogen sources were used for ...

  5. Radiation resistance of organic azo dyes in aqueous solutions

    International Nuclear Information System (INIS)

    Khabarov, V.N.; Kozlov, L.L.

    1987-01-01

    The resistance to the action of the ionizing radiation of aqueous and aqueous-alcoholic solutions of organic mono- and diazo dyes was studied. The radiation chemical yield of decolorization of the dye, determined from the kinetic decolorization curves served as a quantitative criterion of the radiation resistance. The influence of pH, addition of ethanol, hydroquinone, thiourea, glucose and oxygen on the radiation resistance of the azo dyes was studied. An attempt was made to relate the efficiency of radiation decolorization to the chemical nature of the dye

  6. Influence of chemical structures on biodegradation of azo dyes by ...

    African Journals Online (AJOL)

    Influence of chemical structures on biodegradation of azo dyes by Pseudomonas sp. NA Oranusi, CJ Ogugbue. Abstract. No Abstract. Global Journal of Environmental Sciences Vol. 5(1) 2006: 19-25. Full Text: EMAIL FREE FULL TEXT EMAIL FREE FULL TEXT · DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT.

  7. Azo dye reduction by mesophilic and thermophilic anaerobic consortia

    NARCIS (Netherlands)

    Santos, dos A.B.; Madrid, de M.P.; Stams, A.J.M.; Lier, van J.B.; Cervantes, F.J.

    2005-01-01

    The reduction of the azo dye model compounds Reactive Red 2 (RR2) and Reactive Orange 14 (RO14) by mesophilic (30 C) and thermophilic (55 C) anaerobic consortia was studied in batch assays. The contribution of fermentative and methanogenic microorganisms in both temperatures was evaluated in the

  8. Chlorine disinfection of dye wastewater: Implications for a commercial azo dye mixture

    Energy Technology Data Exchange (ETDEWEB)

    Vacchi, Francine Inforcato; Albuquerque, Anjaina Fernandes; Vendemiatti, Josiane Aparecida; Morales, Daniel Alexandre [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil); Ormond, Alexandra B.; Freeman, Harold S. [Department of Textile Engineering, Chemistry, and Science, North Carolina State University, Raleigh, NC 27695-8301 (United States); Zocolo, Guilherme Juliao; Zanoni, Maria Valnice Boldrin [Departamento de Quimica Analitica, Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Quimica de Araraquara, Araraquara, SP 14801-970 (Brazil); Umbuzeiro, Gisela, E-mail: giselau@ft.unicamp.br [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil)

    2013-01-01

    Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving waters. Chemical treatment of effluents containing azo dyes includes disinfection using chlorine, which can generate compounds of varying eco/genotoxicity. Among the widely known commercial azo dyes for synthetic fibers is C.I. Disperse Red 1. While this dye is known to exist as a complex mixture, reports of eco/genotoxicity involve the purified form. Bearing in mind the potential for adverse synergistic effects arising from exposures to chemical mixtures, the aim of the present study was to characterize the components of commercial Disperse Red 1 and its chlorine-mediated decoloration products and to evaluate their ecotoxicity and mutagenicity. In conducting the present study, Disperse Red 1 was treated with chlorine gas, and the solution obtained was analyzed with the aid of LC-ESI-MS/MS to identify the components present, and then evaluated for ecotoxicity and mutagenicity, using Daphnia similis and Salmonella/microsome assays, respectively. The results of this study indicated that chlorination of Disperse Red 1 produced four chlorinated aromatic compounds as the main products and that the degradation products were more ecotoxic than the parent dye. These results suggest that a disinfection process using chlorine should be avoided for effluents containing hydrophobic azo dyes such commercial Disperse Red 1. -- Highlights: Black-Right-Pointing-Pointer Aqueous solutions of Disperse Red 1 were treated with chlorine. Black-Right-Pointing-Pointer The chlorination products of Disperse Red 1 were identified using LC-ESI-MS/MS. Black-Right-Pointing-Pointer Daphnia and Salmonella/microsome were employed for eco/genotoxicity testing. Black-Right-Pointing-Pointer The chlorinated dye was more mutagenic

  9. Chlorine disinfection of dye wastewater: Implications for a commercial azo dye mixture

    International Nuclear Information System (INIS)

    Vacchi, Francine Inforçato; Albuquerque, Anjaina Fernandes; Vendemiatti, Josiane Aparecida; Morales, Daniel Alexandre; Ormond, Alexandra B.; Freeman, Harold S.; Zocolo, Guilherme Julião; Zanoni, Maria Valnice Boldrin; Umbuzeiro, Gisela

    2013-01-01

    Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving waters. Chemical treatment of effluents containing azo dyes includes disinfection using chlorine, which can generate compounds of varying eco/genotoxicity. Among the widely known commercial azo dyes for synthetic fibers is C.I. Disperse Red 1. While this dye is known to exist as a complex mixture, reports of eco/genotoxicity involve the purified form. Bearing in mind the potential for adverse synergistic effects arising from exposures to chemical mixtures, the aim of the present study was to characterize the components of commercial Disperse Red 1 and its chlorine-mediated decoloration products and to evaluate their ecotoxicity and mutagenicity. In conducting the present study, Disperse Red 1 was treated with chlorine gas, and the solution obtained was analyzed with the aid of LC–ESI-MS/MS to identify the components present, and then evaluated for ecotoxicity and mutagenicity, using Daphnia similis and Salmonella/microsome assays, respectively. The results of this study indicated that chlorination of Disperse Red 1 produced four chlorinated aromatic compounds as the main products and that the degradation products were more ecotoxic than the parent dye. These results suggest that a disinfection process using chlorine should be avoided for effluents containing hydrophobic azo dyes such commercial Disperse Red 1. -- Highlights: ► Aqueous solutions of Disperse Red 1 were treated with chlorine. ► The chlorination products of Disperse Red 1 were identified using LC–ESI-MS/MS. ► Daphnia and Salmonella/microsome were employed for eco/genotoxicity testing. ► The chlorinated dye was more mutagenic than the dye itself. ► Chlorination should be avoided in effluents containing azo-dyes.

  10. Re-evaluation of azo dyes as food additives

    DEFF Research Database (Denmark)

    Pratt, Iona; Larsen, John Christian; Mortensen, Alicja

    2013-01-01

    additives to be assessed by the Scientific Committee on Food, many years ago, (ii) because of concern regarding possible health effects of artificial colours arising since the original evaluations.Concerns includedbehavioural effects in children, allergic reactions, genotoxicity and possible carcinogenicity......Aryl azo compounds are widely used as colorants (azo dyes) in a wide range of products including textiles, leather, paper, cosmetics, pharmaceuticals and food.As part of its systematic re-evaluation of food additives, the European Food Safety Authority (EFSA) has carried out new risk assessments...

  11. Understanding effects of chemical structure on azo dye decolorization characteristics by Aeromonas hydrophila

    Energy Technology Data Exchange (ETDEWEB)

    Hsueh, Chung-Chuan [Department of Chemical and Materials Engineering, National I-Lan University, I-Lan 260, Taiwan (China); Chen, Bor-Yann, E-mail: bychen@niu.edu.tw [Department of Chemical and Materials Engineering, National I-Lan University, I-Lan 260, Taiwan (China); Yen, Chia-Yi [Department of Chemical and Materials Engineering, National I-Lan University, I-Lan 260, Taiwan (China)

    2009-08-15

    This novel comparative study tended to disclose how the molecular structures present in seven azo dyes including two types of azo dyes (i.e., naphthol type azo dyes - Reactive Black 5 (RB 5), Reactive Blue 171 (RB 171), Reactive Green 19 (RG19), Reactive Red 198 (RR198), Reactive Red 141 (RR141) and non-naphthol type azo dyes - Direct Yellow 86 (DY86), Reactive Yellow 84 (RY84)) affected color removal capability of Aeromonas hydrophila. Generally speaking, the decolorization rate of naphthol type azo dye with hydroxyl group at ortho to azo bond was faster than that of non-naphthol type azo dye without hydroxyl group, except of RG19. The azo dyes with electron-withdrawing groups (e.g., sulfo group in RR198, RB5 and RR141) would be easier to be decolorized than the azo dyes with the electron-releasing groups (e.g., -NH-triazine in RB171 and RG19). In addition, the azo dyes containing more electron-withdrawing groups (e.g., RR198, RB5 and RR141) showed significantly faster rate of decolorization. The azo dyes with electron-withdrawing groups (e.g., sulfo group) at para and ortho to azo bond (e.g., RR198, RB5 and RR141) could be more preferred for color removal than those at meta (e.g., DY86 and RY84). The former azo dyes with para and ortho sulfo group provided more effective resonance effects to withdraw electrons from azo bond, causing azo dyes to be highly electrophilic for faster rates of reductive biodecolorization. However, since the ortho substituent caused steric hindrance near azo linkage(s), azo dyes with para substituent could be more favorable (e.g., SO{sub 2}(CH{sub 2}){sub 2}SO{sub 4}{sup -} in RR198 and RB5) than those with ortho substituent (e.g., sulfo group at RR141) for decolorization. Thus, the ranking of the position for the electron-withdrawing substituent in azo dyes to escalate decolorization was para > ortho > meta. This study suggested that both the positions of substituents on the aromatic ring and the electronic characteristics of

  12. Synthesis, characterization and dyeing assessment of novel acid azo dyes and mordent acid azo dyes based on 2-hydroxy-4-methoxybenzophenone on wool and silk fabrics

    Directory of Open Access Journals (Sweden)

    DHIRUBHAI J. DESAI

    2010-05-01

    Full Text Available Novel acid mono azo and mordent acid mono azo dyes were synthesised by the coupling of diazonium salt solution of different aromatic amines with 2-hydroxy-4-methoxybenzophenone. The resulting dyes were characterized by spectral techniques, i.e., elemental analysis, IR, 1H-NMR and UV–visible spectroscopy. The dyeing performance of all the dyes was evaluated on wool and silk fabrics. The dyeing of chrome pre-treated wool and silk fabrics showed better hues on mordented fabrics. Dyeing of wool and silk fabrics resulted in pinkish blue to red shades with very good depth and levelness. The dyed fabrics showed excellent to very good light, washing, perspiration, sublimation and rubbing fastness. The results of antibacterial studies of chrome pre-treated fabrics revealed that the toxicity of mordented dyes against Escherichia coli, Staphylococcus aureus, Salmonella typhi, Bacillus subtilis bacteria was fairly good.

  13. Analytical procedures for the determination of disperse azo dyes

    Energy Technology Data Exchange (ETDEWEB)

    Betowski, L.D.; Jones, T.L. (Environmental Protection Agency, Las Vegas, NV (USA)); Munslow, W.; Nunn, N.J. (Lockheed Engineering and Management Services Co., Las Vegas, NV (USA))

    1988-09-01

    Disperse Blue 79 is the most widely-used azo dye in the US. Its economic importance for the dye industry and textile industry is very great. Because of its use and potential for degradation to aromatic amines, this compound has been chosen for testing by the Interagency Testing Committee. The authors laboratory has been developing methods for the analytical determination of Disperse Blue 79 and any possible degradation products in wastewater. This work has been taking place in conjunction with the study of the fate of azo dyes in the wastewater treatment processes by the Water Engineering Research Laboratory of the US EPA in Cincinnati. There were various phases for this analytical development. The first step involved purifying the commercial material or presscake to obtain a standard for quantitative determination. A combination of HPLC, TLC and mass spectrometric methods was used to determine purity after extraction and column cleanup. Phase two involved the extraction of the dye from the matrices involved. The third phase was the actual testing of Disperse Blue 79 in the waste activated sludge system and anaerobic digester. Recovery of the dye and any degradation products at each sampling point (e.g., secondary effluent, waste activated sludge) was the goal of this phase.

  14. Dye-sensitized solar cell based on AZO/Ag/AZO multilayer transparent conductive oxide film

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Jin-He; Li, Ying [School of Materials Science and Engineering, Shanghai University, 149 Yanchang Road, Shanghai 200072 (China); Duong, Thanh-Tung; Choi, Hyung-Jin [Department of Materials Engineering, Chungnam National University, Daeduk Science Town, 305-764 Daejeon (Korea, Republic of); Yoon, Soon-Gil, E-mail: sgyoon@cnu.ac.kr [Department of Materials Engineering, Chungnam National University, Daeduk Science Town, 305-764 Daejeon (Korea, Republic of)

    2013-04-15

    Highlights: ► AZO/Ag/AZO (AAA) multilayer was used for working electrode of DSSC cell. ► The 100 nm-thick Nb-doped TiO{sub 2} layer showed a good blocking effect. ► The DSSC cell by AAA TCO material showed the highest efficiency of about 3.25%. -- Abstract: Niobium-doped TiO{sub 2} blocking layer and Al-doped ZnO (AZO)/Ag/AZO (AAA) TCO layers were grown onto glass substrate using pulsed laser deposition (PLD) and direct current (dc)/radio-frequency (rf) sputtering at room temperature, respectively for dye-sensitized solar cell (DSSC) applications. The 100 nm-thick NTO layer showed a blocking effect for the oxygen diffusion into AAA layer and for the recombination of the electrons. The DSSC cell composed of the NTO (100 nm)/AAA (400 nm) showed the highest photo-electrical efficiency of about 3.25%. An insertion of aluminum foil between serrated clip and AAA (100 nm) TCO improved a photo-conversion efficiency of the DSSC.

  15. Dye-sensitized solar cell based on AZO/Ag/AZO multilayer transparent conductive oxide film

    International Nuclear Information System (INIS)

    Qi, Jin-He; Li, Ying; Duong, Thanh-Tung; Choi, Hyung-Jin; Yoon, Soon-Gil

    2013-01-01

    Highlights: ► AZO/Ag/AZO (AAA) multilayer was used for working electrode of DSSC cell. ► The 100 nm-thick Nb-doped TiO 2 layer showed a good blocking effect. ► The DSSC cell by AAA TCO material showed the highest efficiency of about 3.25%. -- Abstract: Niobium-doped TiO 2 blocking layer and Al-doped ZnO (AZO)/Ag/AZO (AAA) TCO layers were grown onto glass substrate using pulsed laser deposition (PLD) and direct current (dc)/radio-frequency (rf) sputtering at room temperature, respectively for dye-sensitized solar cell (DSSC) applications. The 100 nm-thick NTO layer showed a blocking effect for the oxygen diffusion into AAA layer and for the recombination of the electrons. The DSSC cell composed of the NTO (100 nm)/AAA (400 nm) showed the highest photo-electrical efficiency of about 3.25%. An insertion of aluminum foil between serrated clip and AAA (100 nm) TCO improved a photo-conversion efficiency of the DSSC

  16. Metabolism of azo dyes by human skin microbiota.

    Science.gov (United States)

    Stingley, Robin L; Zou, Wen; Heinze, Thomas M; Chen, Huizhong; Cerniglia, Carl E

    2010-01-01

    Reduction of Methyl Red (MR) and Orange II (Or II) by 26 human skin bacterial species was monitored by a rapid spectrophotometric assay. The analysis indicated that skin bacteria, representing the genera Staphylococcus, Corynebacterium, Micrococcus, Dermacoccus and Kocuria, were able to reduce MR by 74-100 % in 24 h, with only three species unable to reduce completely the dye in that time. Among the species tested, only Corynebacterium xerosis was unable to reduce Or II to any degree by 24 h, and only Staphylococcus delphini, Staphylococcus sciuri subsp. sciuri and Pseudomonas aeruginosa were able to reduce completely this dye within 24 h. MR reduction started with early-exponential growth in Staphylococcus aureus and Staphylococcus epidermidis, and around late-exponential/early-stationary growth in P. aeruginosa. Reduction of Or II, Ponceau S and Ponceau BS started during late-exponential/early-stationary growth for all three species. Using liquid chromatography/electrospray ionization mass spectrometry analyses, MR metabolites produced by Staph. aureus, Staph. epidermidis and P. aeruginosa were identified as N,N-dimethyl-p-phenylenediamine and 2-aminobenzoic acid. Searches of available genomic and proteomic data revealed that at least four of the staphylococci in this study, Staphylococcus haemolyticus, Staph. epidermidis, Staphylococcus cohnii and Staphylococcus saprophyticus, have hypothetical genes with 77, 76, 75 and 74 % sequence identity to azo1 encoding an azoreductase from Staph. aureus and hypothetical proteins with 82, 80, 72 and 74 % identity to Azo1, respectively. In addition, Staphylococcus capitis has a protein with 79 % identity to Azo1. Western analysis detected proteins similar to Azo1 in all the staphylococci tested, except Staph. delphini, Staph. sciuri subsp. sciuri and Staphylococcus auricularis. The data presented in this report will be useful in the risk assessment process for evaluation of public exposure to products containing these dyes.

  17. A Novel Preparation Method of Two Polymer Dyes with Low Cytotoxicity

    Directory of Open Access Journals (Sweden)

    Dongjun Lv

    2017-02-01

    Full Text Available A new preparation method of polymer dyes was developed to improve both the grafting degree of the azo dyes onto O-carboxymethyl chitosan (OMCS and the water solubility of prepared polymer dyes. Firstly, the coupling compound of two azo edible colorants, sunset yellow (SY and allura red (AR, was grafted onto OMCS, and then coupled with their diazonium salt. The chemical structure of prepared polymer dyes was determined by Fourier transform-infrared spectroscopy and 1H-NMR, and the results showed that the two azo dyes were successfully grafted onto OMCS. The grafting degree onto OMCS and the water solubility of polymer dyes were tested, and the results showed that they were both improved as expected. The UV-vis spectra analysis results showed that the prepared polymer dyes showed similar color performance with the original azo dyes. Eventually, the cytotoxicity of prepared polymer dyes was tested and compared with the original azo dyes by a cytotoxicity test on human liver cell lines LO2, and the results showed that their grafting onto OMCS significantly reduced the cytotoxicity.

  18. Isolation and screening of azo dye decolorizing bacterial isolates from dye-contaminated textile wastewater

    Directory of Open Access Journals (Sweden)

    Shahid Mahmood

    2011-04-01

    Full Text Available Azo dyes are released into wastewater streams without any pretreatment and pollute water and soilenvironments. To prevent contamination of our vulnerable resources, removal of these dye pollutants is of greatimportance. For this purpose, wastewater samples were collected from dye-contaminated sites of Faisalabad. About200 bacterial isolates were isolated through enrichment and then tested for their potential to remove RemazolBlack-B azo dye in liquid medium. Five bacterial isolates capable of degrading Remazol Black-B azo dye efficientlywere screened through experimentation on modified mineral salt medium. Isolate SS1 (collected from wastewater ofSupreme Textile Industry was able to completely remove the Remazol Black-B dye from the liquid medium in 18 h.Further, the isolate showed the best performance at the dye concentration of 100 mg L-1 medium (pH 7 and attemperature 35oC. Similarly, yeast extract proved to be the best carbon source for decolorization purpose. Theresults imply that the isolate SS1 could be used for the removal of the reactive dyes from textile effluents.

  19. Aerobic Biodegradation Characteristic of Different Water-Soluble Azo Dyes

    Directory of Open Access Journals (Sweden)

    Shixiong Sheng

    2017-12-01

    Full Text Available This study investigated the biodegradation performance and characteristics of Sudan I and Acid Orange 7 (AO7 to improve the biological dye removal efficiency in wastewater and optimize the treatment process. The dyes with different water-solubility and similar molecular structure were biologically treated under aerobic condition in parallel continuous-flow mixed stirred reactors. The biophase analysis using microscopic examination suggested that the removal process of the two azo dyes is different. Removal of Sudan I was through biosorption, since it easily assembled and adsorbed on the surface of zoogloea due to its insolubility, while AO7 was biodegraded incompletely and bioconverted, the AO7 molecule was decomposed to benzene series and inorganic ions, since it could reach the interior area of zoogloea due to the low oxidation-reduction potential conditions and corresponding anaerobic microorganisms. The transformation of NH3-N, SO42− together with the presence of tryptophan-like components confirm that AO7 can be decomposed to non-toxic products in an aerobic bioreactor. This study provides a theoretical basis for the use of biosorption or biodegradation mechanisms for the treatment of different azo dyes in wastewater.

  20. Abatement of Azo Dye from Wastewater Using Bimetal-Chitosan

    Directory of Open Access Journals (Sweden)

    Ghorban Asgari

    2013-01-01

    Full Text Available We introduce a new adsorbent, bimetallic chitosan particle (BCP that is successfully synthesized and applied to remove the orange II dye from wastewater. The effects of pH, BCP quantity, and contact time are initially verified on the basis of the percentage of orange II removed from the wastewater. Experimental data reveal that the Cu/Mg bimetal and chitosan have a synergistic effect on the adsorption process of the adsorbate, where the dye adsorption by Cu/Mg bimetal, chitosan alone, and bimetal-chitosan is 10, 49, and 99.5%, respectively. The time required for the complete decolorization of orange II by 1 mg/L of BCP is 10 min. The Langmuir model is the best fit for the experimental data, which attains a maximum adsorption capacity of 384.6 mg/g. The consideration of the kinetic behavior indicates that the adsorption of orange II onto the BCP fits best with the pseudo-second-order and Elovich models. Further, the simulated azo dye wastewater can be effectively treated using a relatively low quantity of the adsorbent, 1 mg/L, within a short reaction time of 20 min. Overall, the use of BCP can be considered a promising method for eliminating the azo dye from wastewater effectively.

  1. Solar photoassisted advanced oxidation process of azo dyes.

    Science.gov (United States)

    Prato-Garcia, D; Buitrón, G

    2009-01-01

    Advanced oxidation processes assisted with natural solar radiation in CPC type reactors (parabolic collector compound), was applied for the degradation of three azo dyes: acid orange (AO7), acid red 151 (AR151) and acid blue 113 (AB113). Fenton, Fenton like and ferrioxalate-type complexes showed to be effective for degrade the azo linkage and moieties in different extensions. Initially, the best dose of reagents (Fe(3 + )-H(2)O(2)) was determined through a factorial experimental design, next, using response surface methodologies, the reagent consumption was reduced up to 40%, maintaining in all cases high decolourisation percentages (>98%) after 60 min. of phototreatment. In this work, it was also studied the effect of concentration changes of the influent between 100-300 mg/L and the operation of the photocatalytic process near neutral conditions (pH 6.0-6.5) by using ferrioxalate type complex (FeOx).

  2. Equilibrium and thermodynamics of azo dyes biosorption onto Spirulina platensis

    Directory of Open Access Journals (Sweden)

    G. L. Dotto

    2013-03-01

    Full Text Available The equilibrium and thermodynamics of azo dye (tartrazine and allura red biosorption onto Spirulina platensis biomass were investigated. The equilibrium curves were obtained at 298, 308, 318 and 328 K, and four isotherm models were fitted the experimental data. Biosorption thermodynamic parameters (ΔG, ΔH and ΔS were estimated. The results showed that the biosorption was favored by a temperature decrease. For both dyes, the Sips model was the best to represent the equilibrium experimental data (R²>0.99 and ARE<5.0% and the maximum biosorption capacities were 363.2 and 468.7 mg g-1 for tartrazine and allura red, respectively, obtained at 298 K. The negative values of ΔG and ΔH showed that the biosorption of both dyes was spontaneous, favorable and exothermic. The positive values of ΔS suggested that the system disorder increases during the biosorption process.

  3. Evaluation of biodecolorization of the textile azo dye by halophilic archaea

    Directory of Open Access Journals (Sweden)

    Masoomeh Selseleh Hassan-Kiadehi

    2017-09-01

    Discussion and conclusion: In conclusion, our results indicate that halophilic archaea have very high potential to decolorize azo dyes. Regarding high amounts of salts in textile wastewaters, using such microorganisms which can tolerate the harsh environment in order to decolorize azo dyes, could be a new approach in this field.

  4. Decolourization and degradation of azo Dye, Synozol Red HF6BN ...

    African Journals Online (AJOL)

    Decolourization and degradation of azo Dye, Synozol Red HF6BN, by Pleurotus ostreatus. Sidra Ilyas, Skinder Sultan Sultan, Abdul Rehman. Abstract. The present paper focuses on the use of fungus, Pleurotus ostreatus, to decolorize and degrade azo dye, Synazol Red HF6BN. Decolorization study showed that P.

  5. FACILE SYNTHESIS OF 1-NAPHTHOL AZO DYES WITH NANO ...

    African Journals Online (AJOL)

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    a highly efficient and one pot synthesis of azo dyes based on 1-naphthol under ... known and were identified by comparison of their physical and spectroscopic data with those of ... δ: 16.15 (s, 1H), 8.41 (d, J = 7.6 Hz, 1 H), 8.33 (d, J = 8.8 Hz, 2H), 7.8 (d, .... 86. 81. 77. 70. 65. N2. + IO4. -. O2N. 2d. 96. 93. 90. 85. 79. 73. 69.

  6. Effect of Reactive Black 5 azo dye on soil processes related to C and N cycling

    Directory of Open Access Journals (Sweden)

    Khadeeja Rehman

    2018-05-01

    Full Text Available Azo dyes are one of the largest classes of synthetic dyes being used in textile industries. It has been reported that 15–50% of these dyes find their way into wastewater that is often used for irrigation purpose in developing countries. The effect of azo dyes contamination on soil nitrogen (N has been studied previously. However, how does the azo dye contamination affect soil carbon (C cycling is unknown. Therefore, we assessed the effect of azo dye contamination (Reactive Black 5, 30 mg kg−1 dry soil, bacteria that decolorize this dye and dye + bacteria in the presence or absence of maize leaf litter on soil respiration, soil inorganic N and microbial biomass. We found that dye contamination did not induce any change in soil respiration, soil microbial biomass or soil inorganic N availability (P > 0.05. Litter evidently increased soil respiration. Our study concludes that the Reactive Black 5 azo dye (applied in low amount, i.e., 30 mg kg−1 dry soil contamination did not modify organic matter decomposition, N mineralization and microbial biomass in a silty loam soil.

  7. Decolorization of azo dyes (Direct Blue 151 and Direct Red 31 by moderately alkaliphilic bacterial consortium

    Directory of Open Access Journals (Sweden)

    Sylvine Lalnunhlimi

    2016-03-01

    Full Text Available Abstract Removal of synthetic dyes is one of the main challenges before releasing the wastes discharged by textile industries. Biodegradation of azo dyes by alkaliphilic bacterial consortium is one of the environmental-friendly methods used for the removal of dyes from textile effluents. Hence, this study presents isolation of a bacterial consortium from soil samples of saline environment and its use for the decolorization of azo dyes, Direct Blue 151 (DB 151 and Direct Red 31 (DR 31. The decolorization of azo dyes was studied at various concentrations (100–300 mg/L. The bacterial consortium, when subjected to an application of 200 mg/L of the dyes, decolorized DB 151 and DR 31 by 97.57% and 95.25% respectively, within 5 days. The growth of the bacterial consortium was optimized with pH, temperature, and carbon and nitrogen sources; and decolorization of azo dyes was analyzed. In this study, the decolorization efficiency of mixed dyes was improved with yeast extract and sucrose, which were used as nitrogen and carbon sources, respectively. Such an alkaliphilic bacterial consortium can be used in the removal of azo dyes from contaminated saline environment.

  8. A REVIEW ON EFFICACIOUS METHODS TO DECOLORIZE REACTIVE AZO DYE

    Directory of Open Access Journals (Sweden)

    Jagadeesan Vijayaraghavan

    2013-01-01

    Full Text Available This paper deals with the intensive review of reactive azo dye, Reactive Black 5. Various physicochemical methods namely photo catalysis, electrochemical, adsorption, hydrolysis and biological methods like microbial degradation, biosorption and bioaccumulation have been analyzed thoroughly along with the merits and demerits of each method. Among these various methods, biological treatment methods are found to be the best for decolorization of Reactive Black 5. With respect to dye biosorption, microbial biomass (bacteria, fungi, microalgae, etc, and outperformed macroscopic materials (seaweeds, crab shell, etc. are used for decolorization process. The use of living organisms may not be an option for the continuous treatment of highly toxic organic/inorganic contaminants. Once the toxicant concentration becomes too high or the process operated for a long time, the amount of toxicant accumulated will reach saturation. Beyond this point, an organism's metabolism may be interrupted, resulting in death of the organism. This scenario is not existed in the case of dead biomass, which is flexible to environmental conditions and toxicant concentrations. Thus, owing to its favorable characteristics, biosorption has received much attention in recent years.

  9. Radiolysis of organic triphenylmethane, anthraquinone, xanthene, oxazine, thiazine and azo dyes in polymeric films

    International Nuclear Information System (INIS)

    Khabarov, V.N.; Kozlov, L.L.; Molin, A.A.; Mekhanic, T.V.

    1988-01-01

    Effect of air oxygen and temperature (77 - 323 K) on decolorization radiation-chemical processes of triphenylmethane, anthraquinone, xanthene, oxazine, thiazine and azo dyes in different polymeric matrices is investigated. Radiation decolorization rate for the majority of dyes increases at the irradiation in O 2 presence, which is, presumably, connected with the dye oxidation by the singlet oxygen. The organic dyes manifest the most radiation resistance in polyethyleneterephthalate and polystyrene films

  10. Synthesis, Characterisation and DFT Calculations of Azo-Imine Dyes

    Directory of Open Access Journals (Sweden)

    Sevil Özkınalı

    2017-11-01

    Full Text Available In this study, azo dyes containing an imine group were synthesised by coupling p-hydroxybenzylidene aniline with the diazonium salts of p-toluidine, 4-aminophenol, aniline, p-chloroaniline, p-fluoroaniline, and p-nitroaniline. The compounds were characterised by melting point, elemental, UV-Vis and IR analyses as well as 1H-NMR and 13C-NMR spectroscopies. Moreover, the experimental data were supplemented with density functional theory (DFT calculations. The experimental data on FT-IR and UV–Vis spectra of the compounds were compared with theoretical results. The DFT calculations were performed to obtain the ground state geometries of the compounds using the B3LYP hybrid functional level with 6-311++g(2d,2p basis set. Frontier molecular orbital energies, band gap energies and some chemical reactivity parameters, such as chemical hardness and electronegativity, were calculated and compared with experimental values. A significant correlation was observed between the dipole moment and polarities of the solvents and the absorption wavelength of the compounds.

  11. Synthesis and spectral studies of some novel coumarin based disperse azo dyes

    International Nuclear Information System (INIS)

    Amjad, R.; Khan, S.R.; Naeem, M.

    2009-01-01

    Synthesis of some novel coumarin based azo dyes was carried out by diazotization of heterocyclic amines using nitrosyl sulphuric acid and then coupling them with 7-hydroxy-4-methyl Coumarin. The synthesized dyes when applied on polyester fibers showed moderate to good light fastness and very good to excellent fastness to washing, rubbing, perspiration and sublimation. (author)

  12. Role of brown-rot fungi in the bioremoval of azo dyes under different conditions

    Directory of Open Access Journals (Sweden)

    Naeem Ali

    2010-12-01

    Full Text Available The present study is vital to the understanding of bioremediation of structurally different azo dyes by some unusual Brown-rot fungi. Bioremoval of each dye (20 mg l-1 was tested in two different culture media under static and shaking conditions by taking inocula from different fungi. Fungal strains showed varying dyes removal abilities, though considerable high in case of Acid Red (AR 151(di-azo as compared to Orange (Or II (mono-azo. With an exception of Aspergillus tereus SA3, all the fungal isolates showed higher removal of dyes in SDB. Under static condition, the maximum decolorizing fungal strains were; Aspergillus flavus SA2 (67% and Alternaria spp. SA4 (57% in AR 151, while Penicillium spp. (34 and 33 % in Orange II, in SDB and STE, respectively. Bioremoval of dyes was considerably increased when experiments were shifted from static to shaking mode. It was specifically increased (% in; AR 151 (255 with Penicillium spp., Or II with A. flavus SA2 (112 and Alternaria spp. (111. The primary mechanism of dyes removal proved to be fungal biosorption. However, reduction of dyes (onto fungal with formation of their products (α. naphthol, sulphalinic acid and aniline furthermore revealed that dyes (specifically azo were actually biodegraded.

  13. Ozonation of azo dyes (Orange II and Acid Red 27) in saline media

    International Nuclear Information System (INIS)

    Silva, Alessandra C.; Pic, Jean Stephane; Sant'Anna, Geraldo L.; Dezotti, Marcia

    2009-01-01

    Ozonation of two azo dyes was investigated in a monitored bench scale bubble column reactor (8.5-L), varying liquid media salt content (0, 1, 40 and 100 g L -1 , NaCl). In experiments with Orange II pH was varied (5, 7.5 and 9) but ozonation of Acid Red 27 was performed at pH 7.5. Ozone self-decomposition rate-constant increased with salt concentration. Color removal was very effective and fast achieved under all experimental conditions. For the two azo dyes tested, more than 98% of color intensity was removed in 30-min ozonation assays. However, only partial mineralization of azo dyes (45%-Orange II; 20%-Acid Red 27) was attained in such experiments. The degree of mineralization (TOC removal) was negatively affected by salt concentration. Biodegradation assays conducted by respirometry revealed the inhibitory effect of dye degradation products formed during ozonation.

  14. Electrochemical and optical properties of new soluble dithienylpyrroles based on azo dyes

    International Nuclear Information System (INIS)

    Cihaner, Atilla; Algi, Fatih

    2009-01-01

    Two dithienylpyrroles based on azo dyes, namely 2,5'-dimethyl-[4-(2,5-di-thiophen-2-yl-pyrrol-1-yl)-phenyl]azobenzene (SNS-AB2) and 2,5'-dimethyloxy-[4-(2,5-di-thiophen-2-yl-pyrrol-1-yl)-phenyl]azobenzene (SNS-AB3), were synthesized and their corresponding polymers (PSNS-AB2 and PSNS-AB3) were successfully obtained via electropolymerization. The monomers have lower oxidation potentials (0.75 V and 0.80 V vs. Ag/AgCl for SNS-AB2 and SNS-AB3, respectively) when compared to their analogous. Both monomers exhibited photoisomerism properties under irradiation at 360 nm. During the irradiation process, for example, the color of SNS-AB3 changes from yellow to greenish yellow. The electroactive polymer films have well defined and reversible redox couples with a good cycle stability in both aqueous and organic solutions. The polymer films also exhibited electrochromic behaviors; color changes from yellowish green to dark green for the PSNS-AB2 (λ max = 435 nm and E g = 2.31 eV) and from mustard color to green for PSNS-AB3 (λ max = 430 nm and E g = 2.34 eV). Furthermore, the soluble polymers demonstrated different hues of yellow and green colors

  15. Use of Titanium Dioxide Photocatalysis on the Remediation of Model Textile Wastewaters Containing Azo Dyes

    Directory of Open Access Journals (Sweden)

    Josino Costa Moreira

    2011-12-01

    Full Text Available The photocatalytic degradation of two commercial textile azo dyes, namely C.I Reactive Black 5 and C.I Reactive Red 239, has been studied. TiO2 P25 Degussa was used as catalyst and photodegradation was carried out in aqueous solution under artificial irradiation with a 125 W mercury vapor lamp. The effects of the amount of TiO2 used, UV-light irradiation time, pH of the solution under treatment, initial concentration of the azo dye and addition of different concentrations of hydrogen peroxide were investigated. The effect of the simultaneous photodegradation of the two azo dyes was also investigated and we observed that the degradation rates achieved in mono and bi-component systems were identical. The repeatability of photocatalytic activity of the photocatalyst was also tested. After five cycles of TiO2 reuse the rate of colour lost was still 77% of the initial rate. The degradation was followed monitoring the change of azo dye concentration by UV-Vis spectroscopy. Results show that the use of an efficient photocatalyst and the adequate selection of optimal operational parameters may easily lead to a complete decolorization of the aqueous solutions of both azo dyes.

  16. [The decolorization and biodegrading metabolism of azo dyes by Pseudomonas S-42].

    Science.gov (United States)

    Liu, Z P; Yang, H F

    1989-12-01

    Pseudomonas S-42 was capable of decolorizing azo dyes such as Diamira Brilliant Orange RR(DBO-RR), Direct Brown M (DBM), Eriochrome Brown R(EBR) and so on. The cell suspension, cell-free extract and purified enzyme of Pseud. S-42 could decolorize azo dyes under similar conditions: the optimum pH and temperature laid 7.0 and 37 degrees C respectively. The efficiencies of decolorizing of DBO-RR, DBM, EBR by intact cells stood more than 90%. When the cell concentration was 15 mg(wet)/ml and the reaction time was 5 hours, the decolorizing activity for above three azo dyes by intact cells were 1.75, 2.4, 0.95 micrograms dye/mg cell, respectively. Cell-free extract and purified enzyme could well express the decolorizing activity only under the anaerobic condition and added NADH. Purified enzyme belongs to azoreductase, its molecular weight is about 34,000-2000 daltons, and its Vmax and Km for DBO-RR are 13 mumol.mg protein-1.min-1 and 54 mumol/L. The results of the detection of the biodegrading products of DBO-RR by spectrophotometric and NaNO2 reactional methods showed that the biodegradation of azo dyes was initiated by the reduction cleavage of azo bonds. It was hypothesized that biodegrading metabolism pathway of DBO-RR by Pseudomonas S-42.

  17. Acid-Base Properties of Azo Dyes in Solution Studied Using Spectrophotometry and Colorimetry

    Science.gov (United States)

    Snigur, D. V.; Chebotarev, A. N.; Bevziuk, K. V.

    2018-03-01

    Colorimetry and spectrophotometry with chemometric data processing were used to study the acid-base properties of azo dyes in aqueous solution. The capabilities of both methods were compared. Ionization constants of all the functional groups of the azo compounds studied could be determined relative to the change in the specific color difference depending on the acidity of the medium. The colorimetric functions of ion-molecular forms of azo compounds used as an analytical signal allow us to obtain complete information on the acid-base equilibrium in a wide acidity range.

  18. Biodegradation of azo dyes in cocultures of anaerobic granular sludge with aerobic aromatic amine degrading enrichment cultures

    NARCIS (Netherlands)

    Tan, N.C.G.; Prenefeta-Boldú, F.X.; Opsteeg, J.L.; Lettinga, G.; Field, J.A.

    1999-01-01

    A prerequisite for the mineralization (complete biodegradation) of many azo dyes is a combination of reductive and oxidative steps. In this study, the biodegradation of two azo dyes, 4-phenylazophenol (4-PAP) and Mordant Yellow 10 (4-sulfophenylazo-salicylic acid; MY10), was evaluated in batch

  19. Methods for the analysis of azo dyes employed in food industry--A review.

    Science.gov (United States)

    Yamjala, Karthik; Nainar, Meyyanathan Subramania; Ramisetti, Nageswara Rao

    2016-02-01

    A wide variety of azo dyes are generally added for coloring food products not only to make them visually aesthetic but also to reinstate the original appearance lost during the production process. However, many countries in the world have banned the use of most of the azo dyes in food and their usage is highly regulated by domestic and export food supplies. The regulatory authorities and food analysts adopt highly sensitive and selective analytical methods for monitoring as well as assuring the quality and safety of food products. The present manuscript presents a comprehensive review of various analytical techniques used in the analysis of azo dyes employed in food industries of different parts of the world. A brief description on the use of different extraction methods such as liquid-liquid, solid phase and membrane extraction has also been presented. Copyright © 2015 Elsevier Ltd. All rights reserved.

  20. KINETIC BEHAVIOR OF SOME AZO DYES DECOLORIZATION BY VARIATION OF ZINC OXIDE AND TITANIUM DIOXIDE CONCENTRATIONS

    Directory of Open Access Journals (Sweden)

    Wallace J. C. da Silva

    Full Text Available The decolorization of three monoazo dyes (acid orange 7, direct orange 34, and methyl orange, one diazo dye (direct yellow 86 and one tetraazo dye (direct red 80 were mediated by n-type semiconductors as ZnO and TiO2 under pseudo-first order conditions at 30 ºC. The decolorization rate constants of these azo dyes were determined, varying the semiconductor concentration for the majority of them from 1.0 to 10.0 g L-1. In general, the highest rate constants were displayed for ZnO. This work elucidates that the decolorization capacity depends on the charge, structure, and adsorption of the azo dye on the semiconductor surface as well as the agglomeration of the photocatalyst particles.

  1. Influence of mass transfer and chemical reaction on ozonation of azo dyes

    Energy Technology Data Exchange (ETDEWEB)

    Choi, I.S.; Wiesmann, U. [Dept. of Environmental Engineering, Technical Univ. of Berlin, Berlin (Germany)

    2003-07-01

    Azo dyes can be only mineralised by chemical oxidation. In this paper the oxidation of reactive black 5 (RB 5) and reactive orange 96 (RO 96) with concentrations between 35 and 5700 mgL{sup -1} (RB 5) and between 20 and 2050 mgL{sup -1} (RO 96) is investigated. A lab scale bubble column was used, which was gassed by a mixture of O{sub 2} and O{sub 3}. The oxidation rate was influenced by mass transfer for all dye concentrations used. For lower dye concentrations mass transfer alone was decisive for reaction rate showing an enhancement factor of E {approx} 1. However, in the region of higher dye concentrations, the slope of the decreasing ozone concentration inside the liquid boundary layer increases more and more with increasing dye concentration as a result of a chemical oxidation. Therefore, the enhancement factor depends on the kind and concentration of the azo dyes. For RB 5 as an diazo dye an enhancement factor of E = 9 was observed for 3800 mgL{sup -1}, RO 96 as a mono azo dye with a remarkable higher chemical oxidation rate shows an E = 17 already for 2050 mgL{sup -1}. (orig.)

  2. Evidence for significantly enhancing reduction of Azo dyes in Escherichia coli by expressed cytoplasmic Azoreductase (AzoA) of Enterococcus faecalis.

    Science.gov (United States)

    Feng, J; Heinze, T M; Xu, H; Cerniglia, C E; Chen, H

    2010-05-01

    Although cytoplasmic azoreductases have been purified and characterized from various bacteria, little evidence demonstrating that these azoreductases are directly involved in azo dye reduction in vivo is known. In order to evaluate the contribution of the enzyme to azo dye reduction in vivo, experiments were conducted to determine the effect of a recombinant cytoplasmic azoreductase (AzoA) from Enterococcus faecalis expressed in Escherichia coli on the rate of metabolism of Methyl Red, Ponceau BS and Orange II. The intact cells that contained IPTG induced AzoA had a higher rate of dye reduction with increases of 2 (Methyl Red), 4 (Ponceau BS) and 2.6 (Orange II)-fold compared to noninduced cells, respectively. Metabolites of Methyl Red isolated from induced cultures were identified as N,N-dimethyl-p-phenylenediamine and 2-aminobenzoic acid through liquid chromatography electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) analyses. In conclusion, our data demonstrate that AzoA from Ent. faecalis is capable of increasing the reduction of azo dyes in intact E. coli cells and that cytoplasmic azoreductase is involved in bacterial dye degradation in vivo.

  3. The oxidation of acid azo dye AY 36 by a manganese oxide containing mine waste

    International Nuclear Information System (INIS)

    Clarke, Catherine E.; Kielar, Filip; Johnson, Karen L.

    2013-01-01

    Highlights: ► This study looks at the oxidative breakdown of the amine containing dye acid yellow 36 by a Mn oxide containing mine waste. ► The oxidation proceeds by successive one electron transfers between the dye molecule and the Mn oxide minerals. ► The initial decolorization of the dye is rapid, but does not involve the cleavage of the azo bond. -- Abstract: The oxidative breakdown of acid azo dye acid yellow 36 (AY 36) by a Mn oxide containing mine tailings is demonstrated. The oxidation reaction is pH dependent with the rate of decolorization increasing with decreasing pH. The oxidation reaction mechanism is initiated at the amino moiety and proceeds via successive, one electron transfers from the dye to the Mn oxide minerals. The reaction pathway involves the formation of a number of colorless intermediate products, some of which hydrolyze in a Mn oxide-independent step. Decolorization of the dye is rapid and is observed before the cleavage of the azo-bond, which is a slower process. The terminal oxidation products were observed to be p-benzoquinone and 3-hydroxybenzenesulfonate. The reaction order of the initial decolorization was determined to be pseudo fractional order with respect to pH and pseudo first order with respect to dye concentration and Mn tailings’ surface area

  4. Decolorization of two azo dyes using marine Lysobacter sp. T312D9

    Directory of Open Access Journals (Sweden)

    Khouloud M. I. B.

    2013-01-01

    Full Text Available Aims: Novel azo dye-degrading bacterium T312D9 strain has been isolated from Abou Quir Gulf, Alexandria, Egypt. Methodology and Results: The identification of the isolate by 16S rRNA gene sequencing revealed to be Lysobacter sp. This marine ecofriendly isolate was exploited for its ability to degrade two synthetic azo dyes considered as detrimental pollutants from industrial effluents: congo red and methyl red. Using different dye concentrations showed the highest metabolic activity for complete degradation obtained from 100 to 500 mg/L within 30 h under static condition, also, sustaining higher dye loading of 1 g/L was carried out. The significant induction of enzymes NADH - 2,6-dichloroindophenol (NADH-DCIP reductase and tyrosinaseindicated their prominent role in dye degradation. The biodegradation of two azo dyes were analyzed by gas chromatographicmass spectrum analysis (GC-MS and Fourier transform infrared spectroscopy (FTIR before and after treatment. Toxicity study revealed the much less toxic nature of the metabolites produced after complete decolorization. Conclusion, significance and impact of study: Lysobacter sp T312D9 represent an inexpensive and promising marine bacteria for removal of both methyl and congo red. High sustainable metabolic activity for biodegradation under static condition. NADHDCIPreductase and tyrosinase were significantly induced during biodegradation of dyes. The obtained metabolites revealed to beless toxic in nature which offers a practical biological treatment.

  5. Efficiency of Polymeric Membrane Graphene Oxide-TiO2 for Removal of Azo Dye

    Directory of Open Access Journals (Sweden)

    Elahe Dadvar

    2017-01-01

    Full Text Available Achieving the desired standard of drinking water quality has been one of the concerns across water treatment plants in the developing countries. Processes such as grid chamber, coagulation, sedimentation, clarification, filtration, and disinfection are typically used in water purification plants. Among these methods, unit filtration which employs polymers is one of the new technologies. There have been many studies about the use of semiconductive TiO2 with graphene oxide (GO on the base of different polymeric membranes for the removal of azo dyes, especially methylene blue (MB. Polymeric GO-TiO2 membranes have high photocatalytic, antifouling property and permeate the flux removal of organic pollutants. The aim of this study was to investigate the characteristics of different polymeric membranes such as anionic perfluorinated polymer (Nafion, cellulose acetate, polycarbonate (PC, polysulfone fluoride (PSF, and polyvinylidene fluoride (PVDF. The result of this study showed that the GO-TiO2 membrane can be used in the field of water treatment and will be used for the removal of polycyclic aromatic hydrocarbons (PAHs from wastewater.

  6. Photocatalytic oxidation of a reactive azo dye and evaluation of the ...

    African Journals Online (AJOL)

    The purpose of this study was to investigate the photocatalytic oxidation of a reactive azo dye and determine the improvement in the biodegradability when photocatalytic oxidation was used as a pretreatment step prior to biological treatment. The results obtained from the experiments adding H2O2/TiO2 show that the ...

  7. Reductive decolourisation of azo dyes by mesophilic and thermophilic methanogenic consortia

    NARCIS (Netherlands)

    Cervantes, F.J.; Santos, dos A.B.; Madrid, de M.P.; Stams, A.J.M.; Lier, van J.B.

    2005-01-01

    The contribution of acidogenic bacteria and methanogenic archaea on the reductive decolourisation of azo dyes was assessed in anaerobic granular sludge. Acidogenic bacteria appeared to play an important role in the decolourising processes when glucose was provided as an electron donor; whereas

  8. Comparative study on reaction selectivity of azo dye decolorization by Pseudomonas luteola

    International Nuclear Information System (INIS)

    Hsueh, C.-C.; Chen, B.-Y.

    2007-01-01

    This study is to inspect how the variation of molecular structures and functional groups present in our model azo dyes (i.e., Congo red, Eriochrome black T (EBT), methyl orange, and methyl red) affects biodecolorization capability of Pseudomonas luteola. The most viable decolorization was found at pH 7-9 and the optimal cellular age for the most effective decolorization was 7 days after static incubation in dye-free cultures. In decolorization, the maximal absorption wavelength in UV-vis spectra for the different dye-containing cultures shifted from visible light range towards the ultraviolet visible range. Methyl red was not decolorized in contrast to methyl orange, Congo red, and Eriochrome black T. The sulfonic group para to azo bond (-N=N-) in methyl orange was a strong electron-withdrawing group through resonance to cause an enhancement of color removal to be easily biodecolorized. As a charged carboxyl group on methyl red is at ortho position (i.e., in the proximity) to azo bond, this led to a complete inhibition to decolorization. However, decolorization of Congo red and EBT in the absence of charged group (e.g., hydroxy or amino group) near azo bond was not completely repressed like methyl red. Thus, the presence of electron-withdrawing groups as the substituents on azo dyes enhanced decolorization capability for biodegradability. In addition, Monod kinetic model provided better predictions to all dye decolorization at initial short periods of time due to negligible intermediate formed at initial short time duration, but significant intermediate accumulation took place at longer period of time. In contrast, the decolorization performances of methyl orange at 400 ppm and EBT at 230 ppm were significantly less than those predicted from the Monod kinetic model likely due to accumulated intermediates exceeding the threshold levels for feedback inhibition

  9. Diphenyl (4′-(Aryldiazenylbiphenyl-4-ylamino(pyridin-3-ylmethylphosphonates as Azo Disperse Dyes for Dyeing Polyester Fabrics

    Directory of Open Access Journals (Sweden)

    Mohamed F. Abdel-Megeed

    2013-01-01

    Full Text Available Diphenyl (4′-aminobiphenyl-4-ylamino(pyridin-3-ylmethylphosphonate (1 was synthesized in 88% yield from reaction of pyridine-3-carboxaldehyde with benzidine and triphenylphosphite in the presence of titanium tetrachloride as a catalyst. Diazotization of 1 gave the corresponding diazonium salt 2 which was coupled with several hydroxyl or amino compounds to give the corresponding azo dyes 3–8 in 82–88% yields after crystallization. The dyes produced were applied to polyesters as disperse dyes and their fastness properties were elevated.

  10. Radiation degradation and hemolytic toxicity evaluation of mono azo reactive dyes

    International Nuclear Information System (INIS)

    Saeed, Q.U.; Bhatti, I.A.; Ashraf, A.

    2017-01-01

    Monoazo reactive dyes have been synthesized and subjected to degradation before their application. Advanced oxidation process has been recognized as a promising radiation technology for the remediation of hazardous organic compounds. Radiation induced degradation of two mono azo reactive dyes have been tried at different absorbed dose, 5 kGy,10 kGy and 15 kGy. Aqueous solutions of these dyes were treated with gamma radiation using Cs 137 radiation source at Nuclear Institute of Agriculture and Biology (NIAB) Faisalabad. Dyes were evaluated spectrophotometrically by UV-visible and fourier transform infra red (FT-IR) spectroscopic techniques before and after irradiation to analyse their percentage decolorization and degradation. Maximum percentage decolorization of 93% and 63% was achieved for mono azo dyes D1 and D2 at 15 kGy absorbed dose. Toxicity study of these dyes was also tested by haemolytic activity assay. Percentage haemolytic activity of untreated dyes was found within permissible limit showing non toxicity of dye solutions. (author)

  11. Reduction of azo dyes by flavin reductase from Citrobacter freundii A1

    Directory of Open Access Journals (Sweden)

    Mohd Firdaus Abdul-Wahab

    2012-12-01

    Full Text Available Citrobacter freundii A1 isolated from a sewage treatment facility was demonstrated to be able to effectively decolorize azo dyes as pure and mixed culture. This study reports on the investigation on the enzymatic systems involved. An assay performed suggested the possible involvement of flavin reductase (Fre as an azo reductase. A heterologouslyexpressed recombinant Fre from C. freundii A1 was used to investigate its involvement in the azo reduction process. Three model dyes were used, namely Acid Red 27 (AR27, Direct Blue 15 (DB15 and Reactive Black 5 (RB5. AR27 was found to be reduced the fastest by Fre, followed by RB5, and lastly DB15. Redox mediators nicotinamide adenine dinucleotide (NADH and riboflavin enhance the reduction, suggesting the redox activity of the enzyme. The rate and extent of reduction of the model dyes correlate well with the reduction potentials (Ep. The data presented here strongly suggest that Fre is one of the enzymes responsible for azo reduction in C. freundii A1, acting via an oxidation-reduction reaction.

  12. Degradation of a mono sulfonated azo dye by an integrated bio sorption and anaerobic system

    International Nuclear Information System (INIS)

    Goncalves, L. C.; Campos, R.; Pinheiro, H. M.; Lopes, A.; Ferra, M. I.

    2009-01-01

    A simulated textile effluent containing a mono sulphonated azo dye was fed to an anaerobic bioreactor in which a natural adsorbent, spent brewery grains (SBG), was incorporated. SABG is a by-product of the brewing industry and could act as adsorbent as well an electron shuttle (lignin fraction) in the dye degradation mechanism. Furthermore, it can also work as a conditioner for the anaerobic biomass. The influence of the dye (Acid Orange 7, AO7) concentration (60 and 150 mg/L) and the presence of SBG in the performance of upflow anaerobic sludge blanket reactor (UASB) was evaluated. (Author)

  13. Degradation of a mono sulfonated azo dye by an integrated bio sorption and anaerobic system

    Energy Technology Data Exchange (ETDEWEB)

    Goncalves, L. C.; Campos, R.; Pinheiro, H. M.; Lopes, A.; Ferra, M. I.

    2009-07-01

    A simulated textile effluent containing a mono sulphonated azo dye was fed to an anaerobic bioreactor in which a natural adsorbent, spent brewery grains (SBG), was incorporated. SABG is a by-product of the brewing industry and could act as adsorbent as well an electron shuttle (lignin fraction) in the dye degradation mechanism. Furthermore, it can also work as a conditioner for the anaerobic biomass. The influence of the dye (Acid Orange 7, AO7) concentration (60 and 150 mg/L) and the presence of SBG in the performance of upflow anaerobic sludge blanket reactor (UASB) was evaluated. (Author)

  14. Hollow Palladium Nanoparticles Facilitated Biodegradation of an Azo Dye by Electrically Active Biofilms

    KAUST Repository

    Kalathil, Shafeer; Chaudhuri, Rajib Ghosh

    2016-01-01

    Dye wastewater severely threatens the environment due to its hazardous and toxic effects. Although many methods are available to degrade dyes, most of them are far from satisfactory. The proposed research provides a green and sustainable approach to degrade an azo dye, methyl orange, by electrically active biofilms (EABs) in the presence of solid and hollow palladium (Pd) nanoparticles. The EABs acted as the electron generator while nanoparticles functioned as the electron carrier agents to enhance degradation rate of the dye by breaking the kinetic barrier. The hollow Pd nanoparticles showed better performance than the solid Pd nanoparticles on the dye degradation, possibly due to high specific surface area and cage effect. The hollow cavities provided by the nanoparticles acted as the reaction centers for the dye degradation.

  15. Synthesis and application of new mordent and disperse azo dyes based on 2,4-dihydroxybenzophenone

    Directory of Open Access Journals (Sweden)

    BHARAT C. DIXIT

    2007-02-01

    Full Text Available Novel mordent and disperse azo dyes were prepared by the coupling of various diazo solutions of aromatic amines with 2,4-ihydroxybenzophenone. The resultant dyes were characterized by elemental analyses as well as IR and NMR spectral studies. The UV-visible spectral data have also been iscussed in terms of structural property relationship. The dyeing assessment of all the dyeswas evaluated on wool and polyester textile fibers. The dyeing of chrome treated (i.e., chrome mordented wool and polyesters was also monitored. The results show that a better hue was obtained on mordented fibers. The results of the anti-bacterial properties of the chrome dyes revealed that the toxicity of these dyes against bacteria is fairly good.

  16. Hollow Palladium Nanoparticles Facilitated Biodegradation of an Azo Dye by Electrically Active Biofilms

    KAUST Repository

    Kalathil, Shafeer

    2016-08-04

    Dye wastewater severely threatens the environment due to its hazardous and toxic effects. Although many methods are available to degrade dyes, most of them are far from satisfactory. The proposed research provides a green and sustainable approach to degrade an azo dye, methyl orange, by electrically active biofilms (EABs) in the presence of solid and hollow palladium (Pd) nanoparticles. The EABs acted as the electron generator while nanoparticles functioned as the electron carrier agents to enhance degradation rate of the dye by breaking the kinetic barrier. The hollow Pd nanoparticles showed better performance than the solid Pd nanoparticles on the dye degradation, possibly due to high specific surface area and cage effect. The hollow cavities provided by the nanoparticles acted as the reaction centers for the dye degradation.

  17. Hollow Palladium Nanoparticles Facilitated Biodegradation of an Azo Dye by Electrically Active Biofilms

    Directory of Open Access Journals (Sweden)

    Shafeer Kalathil

    2016-08-01

    Full Text Available Dye wastewater severely threatens the environment due to its hazardous and toxic effects. Although many methods are available to degrade dyes, most of them are far from satisfactory. The proposed research provides a green and sustainable approach to degrade an azo dye, methyl orange, by electrically active biofilms (EABs in the presence of solid and hollow palladium (Pd nanoparticles. The EABs acted as the electron generator while nanoparticles functioned as the electron carrier agents to enhance degradation rate of the dye by breaking the kinetic barrier. The hollow Pd nanoparticles showed better performance than the solid Pd nanoparticles on the dye degradation, possibly due to high specific surface area and cage effect. The hollow cavities provided by the nanoparticles acted as the reaction centers for the dye degradation.

  18. TiO2/beads as a photocatalyst for the degradation of X3B azo dye

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The feasibility of photocatalytic degradation of X3B azo dye by TiO2/beads photocatalyst was studied. The effects of parameters such as the amount of TiO2/beads, airflow, as well as the concentrations of H2O2, Fe3+, Mg2+ and Na+ on the photocatalytic degradation of X3B azo dye were also studied. The results showed that 25 mg/dm3 X3B azo dye can be photocatalytically degraded completely by 30 min illumination with a 375W medium pressure mercury lamp. Adding a small amount of H2O2 or Fe3+, the efficiencies of photocatalytic degradation of X3B azo dye were increased rapidly. The mechanisms of the reaction and the role of the additives were also investigated. After 120 hours TiO2/beads showed no significant loss of the photocatalytic activity.

  19. Novel bio-electro-Fenton technology for azo dye wastewater treatment using microbial reverse-electrodialysis electrolysis cell

    DEFF Research Database (Denmark)

    Li, Xiaohu; Jin, Xiangdan; Zhao, Nannan

    2017-01-01

    Development of sustanaible technologies for treatment of azo dyes containing wastewaters has long been of great interest. In this study, we proposed an innovative concept of using microbial reverse-electrodialysis electrolysis cell (MREC) based Fenton process to treat azo dye wastewater. In such ......Development of sustanaible technologies for treatment of azo dyes containing wastewaters has long been of great interest. In this study, we proposed an innovative concept of using microbial reverse-electrodialysis electrolysis cell (MREC) based Fenton process to treat azo dye wastewater....... In such MREC-Fenton integrated process, the production of H2O2 which is the key reactant of fenton-reaction was driven by the electrons harvested from the exoelectrogens and salinity-gradient between sea water and fresh water in MREC. Complete decolorization and mineralization of 400 mg L-1 Orange G...

  20. Research on Synthesis of New Azo Calix[4]arene and its Dyeing Properties

    Directory of Open Access Journals (Sweden)

    Tang Jun

    2015-01-01

    Full Text Available With the raw materials of calix[4]arene, benzocaine, tricaine and procaine hydrochloride, three new azo calix[4]arene derivatives—6a, 6b and 6c are synthesized by diazotization–coupling reaction of an aromatic amine, with its yield of 83%, 81% and 83% respectively. The structural characterization is in a way of IR, 1H NMR and elemental analysis. This paper investigates the spectral properties of azo calix[4]arene derivatives under different solution pH conditions through the UV–visible spectroscopy, and researches the dyeing properties through the dyeing curve, color yield test and fastness test. The results show that, with the increase of pH value, the azo calix[4]arene derivatives—6a, 6b and 6c form azo–hydrazone tautomeric isomers with the maximum absorption peak redshift; the dyeing effect of the compound is good, of which the dye–uptake rate of the compound 6a is as high as 78%; the surface depth of color yield is 2.798, and the dry and wet rubbing fastness and the soaping fastness are respectively 4, which is a better disperse dye.

  1. The Comparative Study on the Rapid Decolorization of Azo, Anthraquinone and Triphenylmethane Dyes by Anaerobic Sludge

    Directory of Open Access Journals (Sweden)

    Daizong Cui

    2016-10-01

    Full Text Available An anaerobic sludge (AS, capable of decolorizing a variety of synthetic dyes, was acclimated and is reported here. The sludge presented a much better dye decolorizing ability than that of different individual strains. A broad spectrum of dyes could be decolorized by the sludge. Continuous decolorization tests showed that the sludge exhibited the ability to decolorize repeated additions of dye. The chemical oxygen demand (COD removal rate of the dye wastewater reached 52% after 12 h of incubation. Polymerase chain reaction and denaturing gradient gel electrophoresis (PCR-DGGE profiles revealed that the microbial community changed as a result of varying initial concentrations of dyes. Phylogenetic analysis indicated that microbial populations in the sludge belonged to the phyla Acidobacteria, Firmicutes, Bacteroidetes, Chloroflexi and Proteobacteria. The degradation products of the three types of dye were identified. For azo dyes, the anaerobic sludge converted Methyl Orange to N,N-dimethylbenzene-1,4-diamine and 4-aminobenzenesulfonic acid; for triphenylmethane dyes, after Malachite Green was decolorized, the analyzed products were found to be a mixture of N,N-dimethylbenzenamine, 3-dimethyl-aminophenol and 4-dimethylaminobenzophenone; for anthraquinone dyes, two products (acetophenone and 2-methylbenzoic acid were observed after Reactive Blue 19 decolorization. Together, these results suggest that the anaerobic sludge has promising potential for use in the treatment of industrial wastewater containing various types of dyes.

  2. The Comparative Study on the Rapid Decolorization of Azo, Anthraquinone and Triphenylmethane Dyes by Anaerobic Sludge.

    Science.gov (United States)

    Cui, Daizong; Zhang, Hao; He, Rubao; Zhao, Min

    2016-10-28

    An anaerobic sludge (AS), capable of decolorizing a variety of synthetic dyes, was acclimated and is reported here. The sludge presented a much better dye decolorizing ability than that of different individual strains. A broad spectrum of dyes could be decolorized by the sludge. Continuous decolorization tests showed that the sludge exhibited the ability to decolorize repeated additions of dye. The chemical oxygen demand (COD) removal rate of the dye wastewater reached 52% after 12 h of incubation. Polymerase chain reaction and denaturing gradient gel electrophoresis (PCR-DGGE) profiles revealed that the microbial community changed as a result of varying initial concentrations of dyes. Phylogenetic analysis indicated that microbial populations in the sludge belonged to the phyla Acidobacteria, Firmicutes, Bacteroidetes, Chloroflexi and Proteobacteria. The degradation products of the three types of dye were identified. For azo dyes, the anaerobic sludge converted Methyl Orange to N , N -dimethylbenzene-1,4-diamine and 4-aminobenzenesulfonic acid; for triphenylmethane dyes, after Malachite Green was decolorized, the analyzed products were found to be a mixture of N , N -dimethylbenzenamine, 3-dimethyl-aminophenol and 4-dimethylaminobenzophenone; for anthraquinone dyes, two products (acetophenone and 2-methylbenzoic acid) were observed after Reactive Blue 19 decolorization. Together, these results suggest that the anaerobic sludge has promising potential for use in the treatment of industrial wastewater containing various types of dyes.

  3. Synthesis and antitumor evaluation of thiophene based azo dyes incorporating pyrazolone moiety

    Directory of Open Access Journals (Sweden)

    Moustafa A. Gouda

    2016-03-01

    Full Text Available A series of thiophene incorporating pyrazolone moieties 5a–f and 6a–c were synthesized via diazo coupling of diazonium salt of 3-substituted-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophenes 1a–c with 3-methyl-1H-pyrazol-5(4H-one, 3-methyl-1-phenyl-1H-pyrazol-5(4H-one or 3-amino-1H-pyrazol-5(4H-one, respectively. Newly synthesized dyes were applied to polyester fabric as disperse dyes in which their color measurements and fastness properties were evaluated. These dyes showed generally red to blue shifted color with high extinction coefficient in comparison with aniline-based azo dyes. The antitumor activity of the synthesized dyes was evaluated. The results showed clearly that most of them exhibited good activity and compounds 5c and 5d exhibited moderate activity.

  4. Degradation of azo dyes by sequential Fenton's oxidation and aerobic biological treatment

    International Nuclear Information System (INIS)

    Tantak, Nilesh P.; Chaudhari, Sanjeev

    2006-01-01

    A two stage sequential Fenton's oxidation followed by aerobic biological treatment train was used to achieve decolorization and to enhance mineralization of azo dyes, viz. Reactive Black 5 (RB5), Reactive Blue 13 (RB13), and Acid Orange 7 (AO7). In the first stage, Fenton's oxidation process was used while in the second stage aerobic sequential batch reactors (SBRs) were used as biological process. Study was done to evaluate effect of pH on Fenton's oxidation process. Results reveal that pH 3 was optimum pH for achieving decolorization and dearomatization of dyes by Fenton's process. Degradation of dye was assessed by COD reduction and reduction in aromatic amines (naphthalene chromophores) which was measured by reduction in absorbance at 200 nm. More than 95% of color was removed with Fenton's oxidation process in all dyes. In overall treatment train 81.95, 85.57, and 77.83% of COD reduction was achieved in RB5, RB13, and AO7 dyes, respectively. In the Fenton's oxidation process 56, 24.5, and 80% reduction in naphthalene group was observed in RB5, RB13, and AO7, respectively, which further increased to 81.34, 68.73, and 92% after aerobic treatment. Fenton's oxidation process followed by aerobic SBRs treatment sequence seems to be viable method for achieving significant degradation of azo dye

  5. Analysis of electrode microbial communities in an up-flow bioelectrochemical system treating azo dye wastewater

    International Nuclear Information System (INIS)

    Cui, Min-Hua; Cui, Dan; Gao, Lei; Cheng, Hao-Yi; Wang, Ai-Jie

    2016-01-01

    Bioelectrochemical system (BES) is a rapidly developing technology covering contamination remediation, resource recovery and power generation. Electrode biofilms play a key role in BES operation. In this work, a single chamber up-flow bioelectrochemical system (UBES) was assembled with two preinoculated anodes and two raw cathodes for azo dye wastewater treatment. Microbial community structures of these electrodes after long-term operation (more than 200 days) were carried out by high-throughput Illumina 16S rRNA gene MiSeq sequencing platform. Microorganisms belonging to Enterobacter, Desulfovibrio and Enterococcus, which are capable of bidirectional extracellular electron transfer, were found to be the dominant members in all biofilms. Neither the polarity nor the position of the electrodes obviously altered the microbial community structures. This study provides a feasible strategy to build electrode active biofilms in a BES for azo dye wastewater treatment and gives great inspirations to bring this technology closer to application.

  6. Dyeing of Polyester with Disperse Dyes: Part 2. Synthesis and Dyeing Characteristics of Some Azo Disperse Dyes for Polyester Fabrics

    Directory of Open Access Journals (Sweden)

    Alya M. Al-Etaibi

    2016-06-01

    Full Text Available 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.

  7. Incorporation of Kojic Acid-Azo Dyes on TiO2 Thin Films for Dye Sensitized Solar Cells Applications

    Directory of Open Access Journals (Sweden)

    Carolynne Zie Wei Sie

    2017-01-01

    Full Text Available Sensitization of heavy metal free organic dyes onto TiO2 thin films has gained much attention in dye sensitized solar cells (DSSCs. A series of new kojic acid based organic dyes KA1–4 were synthesized via nucleophilic substitution of azobenzene bearing different vinyl chains A1–4 with kojyl chloride 4. Azo dyes KA1–4 were characterized for photophysical properties employing absorption spectrometry and photovoltaic characteristic in TiO2 thin film. The presence of vinyl chain in A1–4 improved the photovoltaic performance from 0.20 to 0.60%. The introduction of kojic acid obtained from sago waste further increases the efficiency to 0.82–1.54%. Based on photovoltaic performance, KA4 achieved the highest solar to electrical energy conversion efficiency (η = 1.54% in the series.

  8. A New Nano Silica Gel Supported by Thionyl Chloride as a Solid Acid for the Efficient Diazotization of Aniline Derivatives: Application and Synthesis of Azo Dyes

    Directory of Open Access Journals (Sweden)

    Mohammad Mirjalili

    2012-01-01

    Full Text Available A new nano silicagel supported by thionyl chloride as a solid acid was synthesized and used as a increasing the production yield of dye to affect the efficient diazotization of arylamines. The diazonium salts thus obtained were coupled, using standard experimental procedures, to anilines and naphthols to afford the requisite azo dyes in good yield. The diazotization and subsequent azo-coupling generated the related azo dyes at low temperature in short reaction times with a simple experimental procedure.

  9. Polymer dye lasers

    DEFF Research Database (Denmark)

    Balslev, Søren

    2006-01-01

    , elektronstrålelithografi og Röntgenstrålelithografi. Andre polymerer er også blevet formgivet via ”nanoimprint” lithografi for at skabe laserresonatorer. En række lasere, både baseret på et flydende forstærkningsmedium og et faststof forstærkningsrmedium er blevet udviklet. Laserne giver både lys i flere ”modes” og i een......Formålet med dette Ph.D. arbejde har været at udvikle miniaturiserede polymer farvestoflasere, egnet til at blive integreret i mikrochips som også indeholder andre polymerstrukturer – som for eksempel kan findes i ”Laboratorie-på-en-chip” kredsløb. Lasernes funktion skal være at levere lys til...... meget følsomme sensorformål, og at undgå at skulle opliniere eksterne lyskilder til sensorer på polymerchips. En enkelt type gennemsigtig ”resist” (SU-8) er blevet brugt til at udvikle en række laserresonatorer i polymer. ”Resisten” er blevet formgivet via en række lithografiske teknikker: UV lithografi...

  10. DFT Study of the Structure, Reactivity, Natural Bond Orbital and Hyperpolarizability of Thiazole Azo Dyes

    Directory of Open Access Journals (Sweden)

    Osman I. Osman

    2017-02-01

    Full Text Available The structure, reactivity, natural bond orbital (NBO, linear and nonlinear optical (NLO properties of three thiazole azo dyes (A, B and C were monitored by applying B3LYP, CAM-B3LYP and ωB97XD functionals with 6-311++G** and aug-cc-pvdz basis sets. The geometrical parameters,dipolemoments,HOMO-LUMO(highest occupied molecular orbital,lowest unoccupied molecular orbital energy gaps, absorption wavelengths and total hyperpolarizabilities were investigated in carbon tetrachloride (CCl4 chloroform (CHCl3, dichloromethane (CH2Cl2 and dimethlysulphoxide (DMSO. The donor methoxyphenyl group deviates from planarity with the thiazole azo moiety by ca. 38◦; while the acceptor dicyanovinyl, indandione and dicyanovinylindanone groups diverge by ca. 6◦. The HOMOs for the three dyes are identical. They spread over the methoxyphenyl donor moiety, the thiazole and benzene rings as π-bonding orbitals. The LUMOs are shaped up by the nature of the acceptor moieties. The LUMOs of the A, B and C dyes extend over the indandione, malononitrile and dicyanovinylindanone acceptor moieties, respectively, as π-antibonding orbitals. The HOMO-LUMO splittings showed that Dye C is much more reactive than dyes A and B. Compared to dyes A and B, Dye C yielded a longer maximum absorption wavelength because of the stabilization of its LUMOs relative to those of the other two. The three dyes show solvatochromism accompanied by significant increases in hyperpolarizability. The enhancement of the total hyperpolarizability of C compared to those of A and B is due to the cumulative action of the long π-conjugation of the indanone ring and the stronger electron-withdrawing ability of the dicyanovinyl moiety that form the dicyanovinylindanone acceptor group. These findings are facilitated by a natural bond orbital (NBO technique. The very high total hyperpolarizabilities of the three dyes define their potent nonlinear optical (NLO behaviour.

  11. Biodecolorization of the azo dye Reactive Red 2 by a halotolerant enrichment culture.

    Science.gov (United States)

    Beydilli, M Inan; Pavlostathis, Spyros G

    2007-11-01

    The decolorization of the azo dye Reactive Red 2 (RR2) under anoxic conditions was investigated using a mesophilic (35 degrees C) halotolerant enrichment culture capable of growth at 100 g/L sodium chloride (NaCl). Batch decolorization assays were conducted with the unacclimated halotolerant culture, and dye decolorization kinetics were determined as a function of the initial dye, biomass, carbon source, and an externally added oxidation-reduction mediator (anthraquinone-2,6-disulphonic acid) concentrations. The maximum biomass-normalized RR2 decolorization rate by the halotolerant enrichment culture under batch, anoxic incubation conditions was 26.8 mg dye/mg VSSxd. Although RR2 decolorization was inhibited at RR2 concentrations equal to and higher than 300 mg/L, the halotolerant culture achieved a 156-fold higher RR2 decolorization rate compared with a previously reported, biomass-normalized RR2 decolorization rate by a mixed mesophilic (35 degrees C) methanogenic culture in the absence of NaCl. Decolorization kinetics at inhibitory RR2 levels were described based on the Haldane model (Haldane, 1965). Five repetitive dyeing/decolorization cycles performed using the halotolerant culture and the same RR2 dyebath solution demonstrated the feasibility of biological renovation and reuse of commercial-strength spent reactive azo dyebaths.

  12. Decolorization of direct poly azo dye with nanophotocatalytic UV/NiO process

    Directory of Open Access Journals (Sweden)

    Ali Assadi

    2012-01-01

    Full Text Available Aims: The aim of the present study is to investigate the efficiency of ultraviolet/ nickel oxide (UV/NiO system as one form of advanced oxidation processes (AOP for decolorization of red poly azo. Materials and Methods: This study was conducted as a laboratory scale in a batch mode. Ultraviolet radiation was provided by a low pressure (11 W UV lamp. Effects of various factors including pH, different irradiation durations, different concentration of nickel oxide, and initial dye concentration were evaluated. Results: The results of the UV/NiO system′s assessment showed that UV light alone cannot remove DR 80 dye. Nickel oxide is an effective catalyst in the decolorization of dye with the nanophotocatalytic process. The decolorization efficiency increases with decreasing pH value and the optimum pH value is 4. Fainally, the highest removal efficiency achieved by UV/NiO process for DR 80 dye with concentrations of 25 mg/l and 50 mg/l was 94.3% and 82.2%, respectively. UV/NiO-based decolorization process follows pseudo-second-order reaction kinetics. Conclusions: From the findings of the present study, it can be concluded that UV/NiO process is an effective technique for decolorization of poly azo dye, DR 80, in aqueous solutions.

  13. Decolorization of Remazol Black-B azo dye in soil by fungi

    Directory of Open Access Journals (Sweden)

    Azeem Khalid*, Sadia Batool, Muhammad Tariq Siddique, Zilli Huma Nazli, Riffat Bibi, Shahid Mahmood and Muhammad Arshad

    2011-04-01

    Full Text Available Textile industry is known to release huge amount of dyes in the water and soil environments during the dyeingprocess. The present study was planned with the aim to remove azo dye toxicants from the soil using fungal strains.The fungi were isolated by using Remazol Black-B azo dye as the sole source of C and N. Ten isolates were initiallyselected for testing their decolorization potential in the liquid medium. Three most effective strains were used tostudy the decolorization of Remazol Black-B in soil. The strain S4 was found to be very effective in removing thedye Remazol Black-B from liquid medium as well as in soil suspension. More than 95% decolorization by the strainS4 was observed in soil under optimal incubation conditions. Overall, the dye decolorization was maximum at 100mg dye kg-1 soil at pH 7-8 under static conditions. Glucose, moisture and aeration also affected the decolorizationefficacy of the fungal strain in soil. This study implies that fungi could be used for bioremediation of dyecontaminatedsites.

  14. Photoassisted Electrochemical Treatment of Azo and Phtalocyanine Reactive Dyes in the Presence of Surfactants

    Science.gov (United States)

    Sala, Mireia; López-Grimau, Víctor; Gutiérrez-Bouzán, Carmen

    2016-01-01

    An electrochemical treatment (EC) was applied at different intensities to degrade the chromophoric groups of dyes C.I. Reactive Black 5 (RB5) and C.I. Reactive Blue 7 (Rb7) until uncolored species were obtained. Decolorization rate constants of the azo dye RB5 were higher than the phtalocyanine Rb7 ones. In addition, the EC treatment was more efficient at higher intensities, but these conditions significantly increased the generation of undesirable by-products such as chloroform. The combination of EC with UV irradiation (UVEC) drastically minimized the generation of chloroform. The photo-assisted electrochemical treatment was also able to achieve decolorization values of 99%. Finally, mixtures of dyes and surfactants were treated by EC and UVEC. In the presence of surfactants, the decolorization kinetic of dyes was slowed due to the competitive reactions of surfactants degradation. Both methods achieved total decolorization and in both cases, the generation of haloforms was negligible. PMID:28773335

  15. Effect of silver nanoparticles on photo-induced reorientation of azo groups in polymer films

    International Nuclear Information System (INIS)

    Zhou Jingli; Yang Jianjun; Sun Youyi; Zhang Douguo; Shen Jing; Zhang Qijin; Wang Keyi

    2007-01-01

    A series of polymer films containing azo groups and silver nanoparticles were prepared. Photo-induced reorientation of the film was conducted under irradiation of polarized light with wavelength at 365 nm, 442 nm and 532 nm, respectively. The influence of the concentration of dopant silver on the reorientation of the azo groups was studied. An enhancement of about 50% for the reorientation rate and about 70% for the reorientation amplitude was achieved. From a comparison of the enhancement obtained by irradiating with three different light sources, it was realized that the mechanism for enhancement of reorientation of azo groups is due to plasmon resonance of silver nanoparticles doped in the polymer films

  16. The contribution of fermentative bacteria and methanogenic archaea to azo dye reduction by a thermophilic anaerobic consortium

    NARCIS (Netherlands)

    Santos, dos A.B.; Cervantes, F.J.; Madrid, de M.P.; Bok, de F.A.M.; Stams, A.J.M.; Lier, van J.B.

    2006-01-01

    The contribution of fermentative bacteria and methanogenic archaea to azo dye reduction by a thermophilic anaerobic consortium was studied. Additionally, the effects of different electron-donating substrates and the redox mediator riboflavin on dye reduction were assessed by using either a

  17. Adsorption of the reactive azo dyes onto NH4Cl-induced activated carbon

    Directory of Open Access Journals (Sweden)

    Sakine Shekoohiyan

    2016-03-01

    Full Text Available Background: The efficacy of NH4Cl-induced activated carbon (NAC was examined in order to adsorb RR198, an azo reactive model dye, from an aqueous solution. Methods: The effects of pH (3 to 10, adsorbent dose (0.1 to 1.2 g/L, dye concentration and contact time on the adsorption efficiency were investigated. Results: The results showed that the removal of dye was highest at a solution pH of 7 and a powder dose of 1.1 g/L. The 85.9%, 72.6% and 65.4% removal of RR198 was obtained for a concentration of 25, 50 and 100 mg/L, respectively, at a relatively short contact time of 30 minutes, and at optimum pH and NAC concentrations of 1 g/L. The experimental data for kinetic analysis illustrated a best fit to the pseudo-second-order model. The study data on equilibrium were modeled using Langmuir, Freundlich and Dubinin–Radushkevich models; the Langmuir equation provided the best fit for the data. Conclusion: Therefore, the NAC appears to be an efficient and appropriate adsorbent for the removal of reactive azo dyes from waste streams.

  18. An Improved Method for Removal of Azo Dye Orange II from Textile Effluent Using Albumin as Sorbent

    Directory of Open Access Journals (Sweden)

    Tadashi Ohashi

    2012-11-01

    Full Text Available Azo dyes are generally resistant to biodegradation due to their complex structures. Acid orange II is one of the most widely used dyes in the textile industry. The influence of bovine serum albumin (BSA in different concentrations, pH, and time of contact on Orange II was investigated using kinetics and adsorption-isotherm experiments. The results showed that the maximum colour removed from dye/albumin was 99.50% and that a stable dye-protein complex had been formed at pH 3.5 and in a proportion of 1:3 (v/v, respectively. The synthetic effluent did not show toxicity to the microcrustacean Artemia salina, and showed a CL50 equal to 97 µg/mL to azo dye orange II. Additionally, the methodology was effective in removing the maximum of orange II using BSA by adsorption at pH 3.5 which mainly attracted ions to the azo dye during the adsorption process. This suggests that this form of treatment is economical and easy to use which potentially could lead to bovine serum albumin being used as a sorbent for azo dyes.

  19. Spatial variation of electrode position in bioelectrochemical treatment system: Design consideration for azo dye remediation.

    Science.gov (United States)

    Yeruva, Dileep Kumar; Shanthi Sravan, J; Butti, Sai Kishore; Annie Modestra, J; Venkata Mohan, S

    2018-05-01

    In the present study, three bio-electrochemical treatment systems (BET) were designed with variations in cathode electrode placement [air exposed (BET1), partially submerged (BET2) and fully submerged (BET3)] to evaluate azo-dye based wastewater treatment at three dye loading concentrations (50, 250 and 500 mg L -1 ). Highest dye decolorization (94.5 ± 0.4%) and COD removal (62.2 ± 0.8%) efficiencies were observed in BET3 (fully submerged electrodes) followed by BET1 and BET2, while bioelectrogenic activity was highest in BET1 followed by BET2 and BET3. It was observed that competition among electron acceptors (electrode, dye molecules and intermediates) critically regulated the fate of bio-electrogenesis to be higher in BET1 and dye removal higher in BET3. Maximum half-cell potentials in BET3 depict higher electron acceptance by electrodes utilized for dye degradation. Study infers that spatial positioning of electrodes in BET3 is more suitable towards dye remediation, which can be considered for scaling-up/designing a treatment plant for large-scale industrial applications. Copyright © 2018 Elsevier Ltd. All rights reserved.

  20. Removal of azo and anthraquinone reactive dyes from industrial wastewaters using MgO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Moussavi, Gholamreza, E-mail: Moussavi@modares.ac.ir [Department of Environmental Health, School of Medical Sciences, Tarbiat Modares University, Tehran (Iran, Islamic Republic of); Mahmoudi, Maryam [Department of Environmental Health, School of Medical Sciences, Tarbiat Modares University, Tehran (Iran, Islamic Republic of)

    2009-09-15

    In the present investigation, a porous MgO powder was synthesized and tested for the removal of dyes from aqueous solution. The size of the MgO particles was in the range of 38-44 nm, with an average specific surface area of 153.7 m{sup 2}/g. Adsorption of reactive blue 19 and reactive red 198 was conducted to model azo and anthraquinone dyes at various MgO dosages, dye concentrations, solution pHs and contact times in a batch reactor. Experimental results indicate that the prepared MgO powder can remove more than 98% of both dyes under optimum operational conditions of a dosage of 0.2 g, pH 8 and a contact time of 5 min for initial dye concentrations of 50-300 mg/L. The isotherm evaluations revealed that the Langmuir model attained better fits to the experimental equilibrium data than the Freundlich model. The maximum predicted adsorption capacities were 166.7 and 123.5 mg of dye per gram of adsorbent for RB 19 and RR 198, respectively. In addition, adsorption kinetic data followed a pseudo-second-order rate for both tested dyes.

  1. Radiolysis of Reactive AZO Dyes in Aqueous Solution

    International Nuclear Information System (INIS)

    Bagyo, Agustin NM; Winarti-Andayani; Hendig-Winarno; Ermin-Katrin; Soebianto, Yanti S

    2004-01-01

    The effects of radiation on aerated reactive dye solutions i.e Cibacron Violet, Cibacron Orange and Cibacron Yellow solutions have been studied. Parameters analysis were the change of pH after radiation, the change of absorption, degradation products and effects of pH on the radiolysis. The uv-vis absorption of solutions were observed before and after irradiation. pH variation was done from pHs 3, 5, 7, 9 and 12. Irradiation was done at doses of 0, 2, 4, 6, 8 and 10 kGy with dose rate of 5 kGy/h and was determined by a Fricke dosimeter. HPLC with UV detector was used to analyze the degradation products. Oxalic acid was the main degradation product and small amount of succinic acid was also detected. (author)

  2. Electrochemical characterization of azo dye (E)-1-(4-((4-(phenylamino)phenyl)diazenyl)phenyl)ethanone (DPA)

    International Nuclear Information System (INIS)

    Surucu, Ozge; Abaci, Serdar; Seferoğlu, Zeynel

    2016-01-01

    Highlights: • Electrochemical characterization of azo dye DPA was performed. • Pencil graphite electrode was used as working electrode. • Cyclic voltammetry was used to determine the effect of scan rate and pH. • Chronoamperometry was used to determine diffusion constant. • Square wave voltammetry verified the results of cyclic voltammetry. - Abstract: An enormous range of possible dyes are available, especially as the starting molecules are readily available and cheap. As other dye classes become less viable from either an environmental or economic reasons, azo dyes come to the forefront. Therefore, electrochemical characterization of a novel synthesized azo dye (E)-1-(4-((4-(phenylamino) phenyl)diazenyl)phenyl)ethanone was achieved for the first time. Cyclic voltammetry, chronoamperometry and square wave voltammetry techniques were used to investigate the electrochemical behavior and electrocatalytic effect of azo dye (E)-1-(4-((4-(phenylamino) phenyl)diazenyl)phenyl)ethanone at pencil graphite electrode. Cyclic voltammograms were utilized to determine the effect of scan rate and pH on the peak current and peak potential. Chronoamperometry technique was used to determine diffusion constant, D and the type of adsorption isotherms. The kinetics parameters which were the apparent electron transfer rate constant, k s and charge transfer coefficient, α were calculated. Square wave voltammetry was used to verify responses of cyclic voltammetry technique.

  3. Synthesis of silver nanoparticles using bacterial exopolysaccharide and its application for degradation of azo-dyes

    Directory of Open Access Journals (Sweden)

    Chinnashanmugam Saravanan

    2017-09-01

    Full Text Available In this study, the synthesis and characterization of exopolysaccharide-stabilized sliver nanoparticles (AgNPs was carried out for the degradation of industrial textile dyes. Characterization of AgNPs was done using surface plasmon spectra using UV–Vis spectroscopy, X-ray diffraction (XRD and Raman spectroscopy. The morphological nature of AgNPs was determined through transmission electron microscopy (TEM, scanning electron microscopy (SEM and atomic force microscopy (AFM, which indicated that the AgNPs were spherical in shape, with an average size of 35 nm. The thermal behaviour of AgNPs revealed that it is stable up to 437.1 °C and the required energy is 808.2J/g in TGA-DTA analysis. Ability of EPS stabilized AgNPs for degradation of azo dyes such as Methyl orange (MO and Congo red (CR showed that EPS stabilized AgNPs were found to be efficient in facilitating the degradation process of industrial textile dyes. The electron transfer takes place from reducing agent to dye molecule via nanoparticles, resulting in the destruction of the dye chromophore structure. This makes EPS-AgNPs a suitable, cheap and environment friendly candidate for biodegradation of harmful textile dyes.

  4. pI-Control in comparative fluorescence gel electrophoresis (CoFGE) using amphoteric azo dyes

    Czech Academy of Sciences Publication Activity Database

    Hanneken, M.; Šlais, Karel; König, S.

    2015-01-01

    Roč. 8, SEP (2015), s. 36-39 ISSN 2212-9685 Institutional support: RVO:68081715 Keywords : comparative fluorescence gel * electrophoresis * protein grid * azo dyes Subject RIV: CB - Analytical Chemistry, Separation http://ac.els-cdn.com/S2212968515000094/1-s2.0-S2212968515000094-main.pdf?_tid=7c92fa40-56e6-11e5-b36a-00000aab0f01&acdnat=1441798543_19612c0d7466780944bc4ae22173da92

  5. Decolourisations and biodegradations of model azo dye solutions using a sequence batch reactor, followed by ultrafiltration

    DEFF Research Database (Denmark)

    Korenak, J.; Ploder, J.; Trček, J.

    2018-01-01

    RNA gene and ITS1-5.8S rDNA-ITS2 sequence analysis, respectively. Serratia marcescens and Klebsiella oxytoca were the most common bacteria with the highest number present during the aerobic and anaerobic phases of the bioprocess. In addition, a high number of Elizabethkingia miricola, Morganella morganii......, Comamonas testosteroni, Trichosporon sp. and Galactomyces sp. were detected. Taken together, our results demonstrated that the sequencing batch reactor system combined with ultrafiltration is an efficient technique for treatment of wastewater containing azo dye. Moreover, the ultrafiltration effectively...

  6. Thermally and optically tunable lasing properties from dye-doped holographic polymer dispersed liquid crystal in capillaries

    Science.gov (United States)

    Chen, Maozhou; Dai, Haitao; Wang, Dongshuo; Yang, Yue; Luo, Dan; Zhang, Xiaodong; Liu, Changlong

    2018-03-01

    In this paper, we investigated tunable lasing properties from the dye-doped holographic polymer dispersed liquid crystal (HPDLC) gratings in capillaries with thermal and optical manners. The thermally tunable range of the lasing from the dye-doped HPDLC reached 8.60 nm with the temperature ranging from 23 °C to 50 °C. The optically tunable laser emission was achieved by doping azo-dye in HPDLC. The transition of azo-dye from trans- to cis-state could induce the reorientation of LC molecules after UV light irradiation, which resulted in the variation of refractive index contrast of LC-rich/polymer-rich layer in HPDLC. Experimentally, the emission wavelength of lasing showed a blueshift (about 2 nm) coupled with decreasing output intensities. The tunable laser based on HPDLC may enable more applications in laser displays, optical communication, biosensors, etc.

  7. Heterogeneous fenton degradation of azo dyes catalyzed by modified polyacrylonitrile fiber fe complexes: QSPR (quantitative structure peorperty relationship) study.

    Science.gov (United States)

    Li, Bing; Dong, Yongchun; Ding, Zhizhong

    2013-07-01

    The amidoximated polyacrylonitrile (PAN) fiber Fe complexes were prepared and used as the heterogeneous Fenton catalysts for the degradation of 28 anionic water soluble azo dyes in water under visible irradiation. The multiple linear regression (MLR) method was employed to develop the quantitative structure property relationship (QSPR) model equations for the decoloration and mineralization of azo dyes. Moreover, the predictive ability of the QSPR model equations was assessed using Leave-one-out (LOO) and cross-validation (CV) methods. Additionally, the effect of Fe content of catalyst and the sodium chloride in water on QSPR model equations were also investigated. The results indicated that the heterogeneous photo-Fenton degradation of the azo dyes with different structures was conducted in the presence of the amidoximated PAN fiber Fe complex. The QSPR model equations for the dye decoloration and mineralization were successfully developed using MLR technique. MW/S (molecular weight divided by the number of sulphonate groups) and NN=N (the number of azo linkage) are considered as the most important determining factor for the dye degradation and mineralization, and there is a significant negative correlation between MW/S or NN=N and degradation percentage or total organic carbon (TOC) removal. Moreover, LOO and CV analysis suggested that the obtained QSPR model equations have the better prediction ability. The variation in Fe content of catalyst and the addition of sodium chloride did not alter the nature of the QSPR model equations.

  8. Case study of the sonochemical decolouration of textile azo dye Reactive Black 5

    International Nuclear Information System (INIS)

    Vajnhandl, Simona; Le Marechal, Alenka Majcen

    2007-01-01

    The decolouration and mineralization of reactive dye C.I. Reactive Black 5, a well-known representative of non-biodegradable azo dyes, by means of ultrasonic irradiation at 20, 279 and 817 kHz has been investigated with emphasis on the effect of various parameters on decolouration and degradation efficiency. Characterization of the used ultrasound systems was performed using calorimetric measurements and oxidative species monitoring using Fricke and iodine dosimeter. Experiments were carried out with low frequency probe type, and a high-frequency plate type transducer at 50, 100 and 150 W of acoustic power and within the 5-300 mg/L initial dye concentration range. Decolouration, as well as radical production, increased with increasing frequency, acoustic power, and irradiation time. Any increase in initial dye concentration results in decreased decolouration rates. Sonochemical decolouration was substantially depressed by the addition of 2-methyl-2-propanol as a radical scavenger, which suggests radical-induced reactions in the solution. Acute toxicity to marine bacteria Vibrio fischeri was tested before and after ultrasound irradiation. Under the conditions employed in this study, no toxic compounds were detected after 6 h of irradiation. Mineralization of the dye was followed by TOC measurements. Relatively low degradation efficiency (50% after 6 h of treatment) indicates that ultrasound is rather inefficient in overall degradation, when used alone

  9. Isolation, Screening and Development of Local Bacterial Consortia With Azo Dyes Decolourising Capability

    Directory of Open Access Journals (Sweden)

    Khadijah, O.

    2009-01-01

    Full Text Available A total of 1540 bacterial isolates were isolated and screened for their ability to degrade selected azo dyes. Of these, nine isolates were chosen for further studies based on their ability to degrade a wide spectrum of dyes efficiently and rapidly. Several microbial consortia were developed and tested for their effectiveness. Overall the consortia were able to degrade 70 - 100% colour within 72 hours compared to 60 – 97% colour removed by individual isolates. A microbial consortium labelled C15 showed good growth in agitation culture but the colour removal was best in static culture with 80 - 100% colour removed in less than 72 hours. Based on the 16S rRNA sequencing, two of the bacterial isolates in C15 belong to the Chryseobacterium genus while the other one belongs to Flavobacterium genus.

  10. Degradação redutiva de azo-corantes utilizando-se ferro metálico Reductive degradation of azo-dyes by metallic iron

    Directory of Open Access Journals (Sweden)

    Cláudio Lima de Souza

    2006-03-01

    Full Text Available Corantes azo são extensivamente utilizados em processos de tingimento de fibras têxteis, sendo caracterizados por elevada resistência frente a processos aeróbios de biodegradação e, por conseqüência, persistência nos processos convencionais de tratamento de resíduos. Neste trabalho reporta-se a degradação redutiva de corantes azo, utilizando-se ferro metálico. Em condições experimentais otimizadas (pH 7 e 10 g de lã de aço comercial a completa descoloração do corante modelo (preto reativo 5 foi conseguida em um sistema contínuo, operando com tempos de retenção de 6 min. Nestas condições, o ferro solubilizado alcança concentrações compatíveis com os limites impostos pela atual legislação brasileira (12 mg L-1. Trata-se de um resultado bastante promissor, principalmente levando-se em consideração o caráter recalcitrante dos azo corantes e a simplicidade do sistema proposto.Azo dyes are extensively used in textile dying processes and are characterized by extreme resistance to biodegradation and consequently persistence during conventional wastewater treatment processes. In this work the reductive degradation of azo dyes was studied using zero-valent iron. At optimized experimental conditions (pH 7 and 10 g of commercial iron wool complete decolorization of the model dye (reactive black 5 was afforded in a continuous system operating with hydraulic retention time of 6 min. At these conditions the released total soluble iron reaches a concentration compatible with the limits imposed by the current Brazilian legislation (12 mg L-1. That is a very promising result, mainly taking into account the high recalcitrant character of azo dyes and the simplicity of the proposed system.

  11. Microbial dynamics during azo dye degradation in a UASB reactor supplied with yeast extract.

    Science.gov (United States)

    Silva, S Q; Silva, D C; Lanna, M C S; Baeta, B E L; Aquino, S F

    2014-01-01

    The present work aimed to investigate the microbial dynamics during the anaerobic treatment of the azo dye blue HRFL in bench scale upflow anaerobic sludge bed (UASB) reactor operated at ambient temperature. Sludge samples were collected under distinct operational phases, when the reactor were stable (low variation of color removal), to assess the effect of glucose and yeast extract as source of carbon and redox mediators, respectively. Reactors performance was evaluated based on COD (chemical oxygen demand) and color removal. The microbial dynamics were investigated by PCR-DGGE (Polimerase Chain Reaction - Denaturing Gradient of Gel Electrophoresis) technique by comparing the 16S rDNA profiles among samples. The results suggest that the composition of microorganisms changed from the beginning to the end of the reactor operation, probably in response to the presence of azo dye and/or its degradation byproducts. Despite the highest efficiency of color removal was observed in the presence of 500 mg/L of yeast extract (up to 93%), there were no differences regarding the microbial profiles that could indicate a microbial selection by the yeast extract addition. On the other hand Methosarcina barkeri was detected only in the end of operation when the best efficiencies on color removal occurred. Nevertheless the biomass selection observed in the last stages of UASB operation is probably a result of the washout of the sludge in response of accumulation of aromatic amines which led to tolerant and very active biomass that contributed to high efficiencies on color removal.

  12. Removal of Azo Dye from Synthetic Wastewater Using Immobilized Nano-Diatomite Within Calcium Alginate

    Directory of Open Access Journals (Sweden)

    AA Khodabandelou

    2016-03-01

    Full Text Available Introduction: The presence of organic dyes, discharged by textile industries, in aqueous environments can cause detrimental effects on aquatic life and subsequently human health. Therefore, the decolorization of aquatic environments is mandatory to protect the environment. For this reason, in the present study, nano-sized diatomite was immobilized within calcium alginate as a nanocomposite adsorbent for removing organic azo dye (Direct blue 15 from aqueous solutions.  Methods: First of all, Iranian diatomite was grinded in a planetary ball mill equipped with tungsten carbide cup for 20 h to achieve nanoparticles of the diatomite. For the immobilization of nanostructured diatomite, a 2% sodium alginate solution was used. Scanning electron microscopy (SEM, X-ray diffraction (XRD and Fourier transform infra-red (FT-IR spectroscopy were used to characterize immobilized nano-diatomite. Fifty milliliter Erlenmeyer flasks were used as batch flow mode experimental reactors. Working solutions were prepared by the dilution of stock solution (1 g/L to desired concentrations. The effect of different operational parameters including contact time, initial pH, adsorbent dosage and initial dye concentration along with kinetic and isotherm of the adsorption were evaluated. After each experiment, the residual concentration of the dyes was measured spectrophotometrically. Results: As results, the adsorption of organic dye increased with increasing contact time and adsorbent dosage, while increasing initial dye concentrations resulted in decreasing the adsorption. The adsorption of DB-15 was favored at basic PH. The immobilization of diatomite led to enhancing the adsorption of  DB-15 compared to diatomite alone. According to the obtained correlation coefficient, the adsorption of DB-15 obeyed pseudo-second order kinetic model and Langmuir isotherm model. The maximum adsorption capacity of diatomite/alginate nanocomposite for the adsorption of DB-15 were found

  13. Poly(methylmethacrylate) grafted chitosan: An efficient adsorbent for anionic azo dyes

    International Nuclear Information System (INIS)

    Singh, V.; Sharma, A.K.; Tripathi, D.N.; Sanghi, R.

    2009-01-01

    Present study reports on peroxydisulfate/ascorbic acid initiated synthesis of Chitosan-graft-poly(methylmethacrylate) (Ch-g-PMMA) and its characterization by FTIR, XRD and 13 C NMR. The copolymer remained water insoluble even under highly acidic conditions and was evaluated to be an efficient adsorbent for the three anionic azo dyes (Procion Yellow MX, Remazol Brilliant Violet and Reactive Blue H5G) over a wide pH range of 4-10 being most at pH 7. The adsorbent was also found efficient in decolorizing the textile industry wastewater and was much more efficient than the parent chitosan. Equilibrium sorption experiments were carried out at different pH and initial dye concentration values. The experimental equilibrium data for each adsorbent-dye system were successfully fitted to the Langmuir and Freundlich sorption isotherms. Based on Langmuir model Q max for yellow, violet and blue dyes was 250, 357 and 178, respectively. Thermodynamic parameters of the adsorption processes such as ΔG o , ΔH o , and ΔS o were calculated. The negative values of free energy reflected the spontaneous nature of adsorption. The adsorption kinetic data of all the three dyes could be well represented by pseudo-second-order model with the correlation coefficients (R 2 ) being 0.9922, 0.9997 and 0.9862, for direct yellow, reactive violet and blue dye, respectively with rate constants 0.91 x 10 -4 , 1.82 x 10 -4 and 1.05 x 10 -4 g mg -1 min -1 , respectively. At pH 7, parent chitosan also showed pseudo-second-order kinetics. The temperature dependence of dye uptake and the pseudo-second-order kinetics of the adsorption indicated that chemisorption is the rate-limiting step that controls the process

  14. Preparation and morphological and optical characterization of azo-polymer-based SiO2 sonogel hybrid composites

    International Nuclear Information System (INIS)

    Morales-Saavedra, Omar G; Ontiveros-Barrera, Fernando G; Torres-Zúñiga, Vicente; Guadalupe-Bañuelos, José; Ortega-Martínez, Roberto; Rivera, Ernesto; García, Tonatiuh

    2009-01-01

    The well-established catalyst-free sonogel route was successfully implemented to fabricate highly pure, optically active, solid state polymeric azo- dye/SiO 2 -based hybrid composites. Bulk samples exhibit controllable geometrical shapes and monolithic structure with variable dopant concentrations. Since the implemented azo-dye chromophores exhibit a push–pull structure, hybrid film samples were spin-coated on ITO-covered glass substrates; molecular alignment was then performed via electrical poling in order to explore the quadratic nonlinear optical performance of this kind of composite. Comprehensive morphological, spectroscopic and optical characterization of the samples were performed with several experimental techniques: atomic force microscopy, x-ray diffraction and infrared, Raman, photoluminescent and ultraviolet–visible spectroscopies. The linear refractive indices of both bulk and thin film samples were measured according to the Brewster angle technique and a numerical analysis of the transmission spectral data, respectively. Regardless of the low glass transition temperatures of the studied polymers, some hybrid film samples were able to display stable nonlinear optical activity such as second harmonic generation. Results show that the chromophores were satisfactorily embedded into the highly pure SiO 2 sonogel network without significant guest–host molecular interactions, thus preserving their optical properties and producing sol–gel hybrid glasses suitable for optical applications

  15. Degradation of direct azo dye by Cucurbita pepo free and immobilized peroxidase.

    Science.gov (United States)

    Boucherit, Nabila; Abouseoud, Mahmoud; Adour, Lydia

    2013-06-01

    Enzymatic decolourization of the azo dye, Direct Yellow (DY106) by Cucurbita pepo (courgette) peroxidase (CP) is a complex process, which is greatly affected by pH, temperature, enzyme activity and the concentrations of H2O2 and dye. Courgette peroxidase was extracted and its performance was evaluated by using the free-CP (FCP) and immobilized-CP (ICP) forms in the decolourization of DY106. Immobilization of peroxidase in calcium alginate beads was performed according to a strategy aiming to minimize enzyme leakage and keep its activity at a maximum value by optimizing sodium alginate content, enzyme loading and calcium chloride concentration. The initial conditions at which the highest DY106 decolourization yield was obtained were found at pH 2, temperature 20 degrees C, H2O2 dose 1 mmol/L (FCP) and 100 mmol/L (ICP). The highest decolourization rates were obtained for dye concentrations 50 mg/L (FCP) and 80 mg/L (ICP). Under optimal conditions, the FCP was able to decolorize more than 87% of the dye within 2 min. While with ICP, the decolourization yield was 75% within 15 min. The decolourization and removal of DY106 was proved by UV-Vis analysis. Fourier transform infrared (FT-IR) spectroscopy analysis was also performed on DY106 and enzymatic treatment precipitated byproduct.

  16. Synthesis of MoO3 nanoparticles for azo dye degradation by catalytic ozonation

    International Nuclear Information System (INIS)

    Manivel, Arumugam; Lee, Gang-Juan; Chen, Chin-Yi; Chen, Jing-Heng; Ma, Shih-Hsin; Horng, Tzzy-Leng; Wu, Jerry J.

    2015-01-01

    Highlights: • Synthesis of one-dimensional MoO 3 nanostructures using hydrothermal, microwave, and sonochemical methods. • Sonochemical synthesized MoO 3 presents the best efficiency for the dye removal by catalytic ozonation. • Efficient environmental remediation process. - Abstract: One-dimensional molybdenum trioxide nanostructures were prepared in three different approaches, including thermal, microwave, and sonochemical methods. The physicochemical properties of the obtained MoO 3 nanoparticles were investigated by diffused reflectance spectroscopy, X-ray diffraction analysis, field emission scanning electron microscopy, high resolution transmission electron microscopy, and Brunauer–Emmett–Teller surface area analysis. Among the methods as investigated, sonochemical synthesis gave well-dispersed fine MoO 3 nanoparticles compared with the other approaches. All the synthesized MoO 3 nanostructures were examined for the catalytic ozonation to degrade azo dye in aqueous environment. Different performances were obtained for the catalyst prepared in different methods and the catalytic efficiencies were found to be the order of sonochemical, microwave, and then thermal methods. The sonochemical MoO 3 catalyst allowed the total dye removal within 20 min and its good performance was justified according to their higher surface area with higher number of active sites that provide effective dye interaction for better degradation

  17. Biodegradation of carcinogenic textile azo dyes using bacterial isolates of mangrove sediment

    Directory of Open Access Journals (Sweden)

    Guru Prasad Srinivasan

    2014-02-01

    Full Text Available Objective: To evaluate the biodegrading property against carcinogenic azo dyes using bacterial isolates of mangrove sediment. Methods: The bacterial isolates were subjected to submerged fermentation and their growth kinetics were studied. The potential strain was characterized using 16S rDNA sequencing. Results: In the present study, dye degrading bacterial colonies were isolated from the mangrove sediment samples of Parangipettai estuarine area, Tamil Nadu. Of the 30 morphologically different strains isolated, 5 showed antagonistic property. The growth kinetics of the two strains, P1 and G1, which showed potent activity were calculated. One particular isolate (P1 showing promising dye degrading potential in the submerged fermentation was further characterized. The strain was identified as Paenibacillus sp. by 16S rDNA sequencing. Conclusions: This study reveals the less explored microflora of mangrove sediments. The novel strain may further be analyzed and used in the treatment of effluent from dye industry so as to reduce the impact of carcinogenic contaminants.

  18. Light sensitive polymer obtained by dispersion of azo-functionalized POSS nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Miniewicz, A., E-mail: andrzej.miniewicz@pwr.edu.pl [Advanced Materials Engineering and Modelling, Faculty of Chemistry, Wroclaw University of Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw (Poland); Tomkowicz, M.; Karpinski, P.; Sznitko, L. [Advanced Materials Engineering and Modelling, Faculty of Chemistry, Wroclaw University of Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw (Poland); Mossety-Leszczak, B. [Faculty of Chemistry, Rzeszow University of Technology, Al. Powstancow Warszawy 12, 35-959 Rzeszow (Poland); Dutkiewicz, M. [Faculty of Chemistry, Adam Mickiewicz University of Poznan, Umultowska 89 B, 61-614 Poznan (Poland)

    2015-07-29

    Highlights: • Nanocomposite material PMMA containing azo-functionalized POSS has been prepared. • Surface topographies of prepared films are porous and dependent on azo-POSS content. • Photo-induced optical anisotropies both static and dynamic have been characterized. - Abstract: Hybrid inorganic–organic nanoparticles based on cubic siloxane cage (RSiO{sub 3/2}){sub 8}, known as polyhedral oligosilsesquioxane (POSS), have been functionalized by eight groups of azo-benzene mesogens and dispersed in poly(methyl methacrylate) PMMA matrix. Presence of azo-benzene units adds an important light-driven functionality to the system due to their photoisomerization resulting in refractive index and/or absorption changes of the whole system. The polymer films containing various concentrations of azo-POSS nanoparticles show remarkable changes of surface morphology being either transparent (at low POSS concentration) or highly scattering (at high POSS concentration) for visible light. Surface structures were examined by optical microscopy as well as by atomic force microscopy (AFM). Results of photoinduced alignment are discussed in the framework of light-induced modification of the aliphatic chains containing azo-benzene photoisomerizing moieties and self-organization process.

  19. Light sensitive polymer obtained by dispersion of azo-functionalized POSS nanoparticles

    International Nuclear Information System (INIS)

    Miniewicz, A.; Tomkowicz, M.; Karpinski, P.; Sznitko, L.; Mossety-Leszczak, B.; Dutkiewicz, M.

    2015-01-01

    Highlights: • Nanocomposite material PMMA containing azo-functionalized POSS has been prepared. • Surface topographies of prepared films are porous and dependent on azo-POSS content. • Photo-induced optical anisotropies both static and dynamic have been characterized. - Abstract: Hybrid inorganic–organic nanoparticles based on cubic siloxane cage (RSiO 3/2 ) 8 , known as polyhedral oligosilsesquioxane (POSS), have been functionalized by eight groups of azo-benzene mesogens and dispersed in poly(methyl methacrylate) PMMA matrix. Presence of azo-benzene units adds an important light-driven functionality to the system due to their photoisomerization resulting in refractive index and/or absorption changes of the whole system. The polymer films containing various concentrations of azo-POSS nanoparticles show remarkable changes of surface morphology being either transparent (at low POSS concentration) or highly scattering (at high POSS concentration) for visible light. Surface structures were examined by optical microscopy as well as by atomic force microscopy (AFM). Results of photoinduced alignment are discussed in the framework of light-induced modification of the aliphatic chains containing azo-benzene photoisomerizing moieties and self-organization process

  20. Nanoimprinted polymer photonic crystal dye lasers

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Smith, Cameron; Buss, Thomas

    2010-01-01

    Optically pumped polymer photonic crystal band-edge dye lasers are presented. The photonic crystal is a rectangular lattice providing laser feedback as well as an optical resonance for the pump light. The lasers are defined in a thin film of photodefinable Ormocore hybrid polymer, doped...

  1. Decolorization of azo dyes Orange G using hydrodynamic cavitation coupled with heterogeneous Fenton process.

    Science.gov (United States)

    Cai, Meiqiang; Su, Jie; Zhu, Yizu; Wei, Xiaoqing; Jin, Micong; Zhang, Haojie; Dong, Chunying; Wei, Zongsu

    2016-01-01

    The present work demonstrates the application of the combination of hydrodynamic cavitation (HC) and the heterogeneous Fenton process (HF, Fe(0)/H2O2) for the decolorization of azo dye Orange G (OG). The effects of main affecting operation conditions such as the inlet fluid pressure, initial concentration of OG, H2O2 and zero valent iron (ZVI), the fixed position of ZVI, and medium pH on decolorization efficiency were discussed with guidelines for selection of optimum parameters. The results revealed that the acidic conditions are preferred for OG decolorizaiton. The decolorization rate increased with increasing H2O2 and ZVI concentration and decreased with increasing OG initial concentration. Besides, the decolorization rate was strongly dependent on the fixed position of ZVI. The analysis results of degradation products using liquid chromatography-ESI-TOF mass spectrometry revealed that the degradation mechanism of OG proceeds mainly via reductive cleavage of the azo linkage due to the attack of hydroxyl radical. The present work has conclusively established that the combination of HC and HF can be more energy efficient and gives higher decolorization rate of OG as compared with HC and HF alone. Copyright © 2015 Elsevier B.V. All rights reserved.

  2. Ultrasound enhanced activation of peroxydisulfate by activated carbon fiber for decolorization of azo dye.

    Science.gov (United States)

    Huang, Tianyin; Zhang, Ke; Qian, Yajie; Fang, Cong; Chen, Jiabin

    2018-02-20

    Activated carbon fiber (ACF) has become an emerging activator for peroxydisulfate (PDS) to generate sulfate radical (SO 4 •- ). However, the relative low activation efficiency and poor contaminant mineralization limited its widespread application. Herein, ultrasound (US) was introduced to the ACF activated PDS system, and the synergistic effect of US and ACF in PDS activation and the enhancement of contaminant mineralization were investigated. The synergistic effect of US and ACF was observed in the PDS activation to decolorize orange G (OG). The decolorization efficiency increased with increasing ACF loading and US power, and PDS/OG ratio from 1 to 40. The activation energy was determined to be 24.065 kJ/mol. The radical-induced decolorization of OG took place on the surface of ACF, and both SO 4 •- and hydroxyl radical ( • OH) contributed to OG decolorization. The azo bond and naphthalene ring on OG were destructed to other aromatic intermediates and finally mineralized to CO 2 and H 2 O. The introduction of US in the ACF/PDS system significantly enhanced the mineralization of OG. The combination of US and PDS was highly efficient to activate PDS to decolorize azo dyes. Moreover, the introduction of US remarkably improved the contaminant mineralization.

  3. All-fiber maskless lithographic technology to form microcircular interference pattern on Azo polymer film

    Science.gov (United States)

    Kim, Junki; Jung, Yongmin; Oh, Kyunghwan; Chun, Chaemin; Hong, Jeachul; Kim, Dongyu

    2005-03-01

    We report a novel all-fiber, maskless lithograpic technology to form various concentric grating patterns for micro zone plate on azo polymer film. The proposed technology is based on the interference pattern out of the cleaved end of a coreless silica fiber (CSF)-single mode fiber (SMF) composite. The light guided along SMF expands into the CSF segment to generate various circular interference patterns depending on the length of CSF. Interference patterns are experimentally observed when the CSF length is over a certain length and the finer spacing between the concentric rings are obtained for a longer CSF. By using beam propagation method (BPM) package, we could further investigated the concentric interference patterns in terms of intensity distribution and fringe spacing as a function of CSF length. These intereference patterns are directly projected over azo polymer film and their intensity distrubution formed surface relief grating (SRG) patterns. Compared to photoresist films azo polymer layers produce surface relief grating (SRG), where the actual mass of layer is modulated rather than refractive index. The geometric parameters of the CSF length as well as diameter and the spacing between the cleaved end of a CSF and azo polymer film, were found to play a major role to generate various concentric structures. With the demonstration of the circular SRG patterns, we confirmed that the proposed technique do have an ample potential to fabricate micro fresnel zone plate, that could find applications in lens arrays for optical beam formings as well as compact photonic devices.

  4. Biodegradation mechanisms and kinetics of azo dye 4BS by a microbial consortium.

    Science.gov (United States)

    He, Fang; Hu, Wenrong; Li, Yuezhong

    2004-10-01

    A microbial consortium consisting of a white-rot fungus 8-4* and a Pseudomonas 1-10 was isolated from wastewater treatment facilities of a local dyeing house by enrichment, using azo dye Direct Fast Scarlet 4BS as the sole source of carbon and energy, which had a high capacity for rapid decolorization of 4BS. To elucidate the decolorization mechanisms, decolorization of 4BS was compared between individual strains and the microbial consortium under different treatment processes. The microbial consortium showed a significant improvement on dye decolorization rates under either static or shaking culture, which might be attributed to the synergetic reaction of single strains. From the curve of COD values and the UV-visible spectra of 4BS solutions before and after decolorization cultivation with the microbial consortium, it was found that 4BS could be mineralized completely, and the results had been used for presuming the degrading pathway of 4BS. This study also examined the kinetics of 4BS decolorization by immobilized microbial consortium. The results demonstrated that the optimal decolorization activity was observed in pH range between four and 9, temperature range between 20 and 40 degrees C and the maximal specific decolorization rate occurred at 1,000 mg l(-1) of 4BS. The proliferation and distribution of microbial consortium were also microscopically observed, which further confirmed the decolorization mechanisms of 4BS.

  5. Kinetic and equilibrium study of adsorption of di-azo dyes on commercial activated carbon

    International Nuclear Information System (INIS)

    Hyali, E.A.S.A.; Abady, T.G.A.

    2013-01-01

    This research work is concerned with studying the adsorption of a number of di-azo dyes on commercial activated carbon (CAC). The synthesized dyes vary in their structures by the central parts. which are either ortho, meta or para phenvlene diamine. This variation affects the linearity of molecules, their spatial arrangement and electron movement throughout the molecule by resonance. Factors a fleeting adsorption process, such as the efiect of contact time, initial concentration, p1-I of the adsorption medium, adsorbent dose, effect of solvent and temperature were studied. The results indicated that, the adsorption process is fast in the first 10 mm, then gradually decreased with time and approaches maximum within 70-80 min for all the studied dyes. The increase of initial concentration and temperature decreased the adsorption efficiency. The results also shows that, the adsorption is found to be more efficient at low Ph value. The increase of the adsorbent dose increases the adsorption efficiency and decreases its capacity. The variation of solvent (ethanol-water ratio) indicates that the decrease of dielectric constant lowers the adsorption efficiency. The study included application of three adsorption isotherms, Freundlich, Langmuir and Tempkin on the experimental data of the studied systems. The results indicated that, Freundlich isotherm fits better the adsorption data. Kinetic analysis of the adsorption data was also conducted by employing 4 kinetic models; pseudo first order and pseudo second order, Elovich and intra particle diffusion equations. The results obtained conclude that, the studied systems follow the Pseudo second order model. (author)

  6. Poly(acrylamide) functionalized chitosan: An efficient adsorbent for azo dyes from aqueous solutions

    International Nuclear Information System (INIS)

    Singh, Vandana; Sharma, Ajit Kumar; Sanghi, Rashmi

    2009-01-01

    In the present communication we report on the optimization of persulfate/ascorbic acid initiated synthesis of chitosan-graft-poly(acrylamide) (Ch-g-PAM) and its application in the removal of azo dyes. The optimum yield of the copolymer was obtained using 16 x 10 -2 M acrylamide, 3.0 x 10 -2 M ascorbic acid, 2.4 x 10 -3 M K 2 S 2 O 8 and 0.1 g chitosan in 25 mL of 5% aqueous formic acid at 45 ± 0.2 o C. Ch-g-PAM remained water insoluble even under highly acidic conditions and could efficiently remove Remazol violet and Procion yellow dyes from the aqueous solutions over a pH range of 3-8 in contrast to chitosan (Ch) which showed pH dependent adsorption. The adsorption data of the Ch-g-PAM and Ch for both the dyes were modeled by Langmuir and Freundlich isotherms where the data fitted better to Langmuir isotherms. To understand the adsorption behavior of Ch-g-PAM, adsorption of Remazol violet on to the copolymer was optimized and the kinetic and thermodynamic studies were carried out taking Ch as reference. Both Ch-g-PAM and Ch followed pseudo-second-order adsorption kinetics. The thermodynamic study revealed a positive heat of adsorption (ΔH o ), a positive ΔS o and a negative ΔG o , indicating spontaneous and endothermic nature of the adsorption of RV dye on to the Ch-g-PAM. The Ch-g-PAM was found to be very efficient in removing color from real industrial wastewater as well, though the interfering ions present in the wastewater slightly hindered its adsorption capacity. The data from regeneration efficiencies for ten cycles evidenced the high reusability of the copolymer in the treatment of waste water laden with even high concentrations of dye.

  7. Analysis of photoinduced birefringence in azo-dye doped films by a fast imaging technique

    International Nuclear Information System (INIS)

    Marino, Iari-Gabriel; Lottici, Pier Paolo

    2010-01-01

    In photo-birefringent films, the relationship ρ(I) between optical retardation ρ and pump irradiance I may be obtained with imaging techniques applied within a pump-probe setup. However, measurement of ρ(I) are reported only at long irradiation times and low time-resolution. In this paper we describe a polariscopic imaging technique with higher sensitivity (by a factor of ∼ 30), where the probe beam is focused on the entrance pupil of the camera ('Maxwellian view'). The technique is applied to an azo-dye doped polymeric film, obtaining the continuous ρ(I) curve after irradiation times from 10 ms to 240 ms. Exponential functions are fitted against the experimental data both as a function of time and irradiance.

  8. Waste Plant Material as a Potential Adsorbent of a Selected Azo Dye

    Directory of Open Access Journals (Sweden)

    Tomczak Elwira

    2017-06-01

    Full Text Available This paper discusses the adsorption of Direct Orange 26 azo dye on sunflower husk - an agricultural waste product. During the study, sorption kinetics and equilibrium as well as sorption capacity of the husk were investigated. The adsorption kinetics was analyzed using pseudo-first and pseudo-second order equations, which indicated a chemical sorption mechanism. The sorption equilibrium was approximated with the two-parameter Freundlich and Langmuir equations and the three-parameter Redlich-Peterson equation. The main experiments were carried out in a laboratory adsorption column under different process conditions. Experimental data were interpreted with the Thomas model, based on the volumetric flow rate, initial composition of the feed solution and mass of the adsorbent. The results of modeling the adsorption equilibrium, adsorption kinetics and adsorption dynamics were evaluated statistically.

  9. Synthesis and characterization of Mg-based amorphous alloys and their use for decolorization of Azo dyes

    International Nuclear Information System (INIS)

    Iqbal, M; Wang, W H

    2014-01-01

    Mg-based alloys are light weight and have wide range of applications in the automotive industry. These alloys are widely used because of their very attractive physical and mechanical properties and corrosion resistance. The properties and applications can be further improved by changing the nature of materials from crystalline to amorphous. In this study, melt spun ribbons (MSRs) of Mg 70 Zn 25 Ca 5 Mg 68 Zn 27 Ca 5 alloys were prepared by melt spinning technique by using 3-4N pure metals. Characterization of the samples was done by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and energy dispersive x-ray analyzer (EDAX). Microstructural investigations were conducted by using scanning electron microscopy (SEM), atomic force microscopy (AFM) as well as optical and stereo scan microscopy techniques. DSC results showed multistage crystallization. Activation energy was found to be 225 kJ/mol by Kissinger method indicating good thermal stability against crystallization. XRD, DSC, SEM and EDS (energy dispersive spectroscopy) results are agreed very well. In order to study decolorization, the MSRs of Mg 70 Zn 25 Ca 5 Mg 68 Zn 27 Ca 5 alloys were treated repeatedly with various azo dyes at room temperature. In order to compare the results, MSRs of amorphous Zr- and Ni-based metallic glasses were also treated. Reaction of MSRs with azo dyes results in their decolorization in a few hours. Decolorization of azo dyes takes place by introducing amorphous MSRs which results in breaking the -N=N- bonds that exist in dye contents. It is concluded that Mg-based alloys are useful for paint and dye industries and will be beneficial to control water pollution. Comparison of results showed that Mg-based alloys are more efficient than Zr- and Ni-based amorphous alloys for decolorization of azo dyes

  10. Immobilized laccase mediated dye decolorization and transformation pathway of azo dye acid red 27

    OpenAIRE

    Chhabra, Meenu; Mishra, Saroj; Sreekrishnan, Trichur Ramaswamy

    2015-01-01

    Background Laccases have good potential as bioremediating agents and can be used continuously in the immobilized form like many other enzymes. Methods In the present study, laccase from Cyathus bulleri was immobilized by entrapment in Poly Vinyl Alcohol (PVA) beads cross-linked with either nitrate or boric acid. Immobilized laccase was used for dye decolorization in both batch and continuous mode employing a packed bed column. The products of degradation of dye Acid Red 27 were identified by ...

  11. Enzyme-mediated bacterial biodegradation of an azo dye (C.I. Acid blue 113): reuse of treated dye wastewater in post-tanning operations.

    Science.gov (United States)

    Senthilvelan, T; Kanagaraj, J; Panda, R C

    2014-11-01

    "Dyeing" is a common practice used to color the hides during the post-tanning operations in leather processing generating plenty of wastewater. The waste stream containing dye as pollutant is severely harmful to living beings. An azo dye (C.I. Acid Blue 113) has been biodegraded effectively by bacterial culture mediated with azoreductase enzyme to reduce the pollution load in the present investigation. The maximum rate of dye degradation was found to be 96 ± 4 and 92 ± 4 % for the initial concentrations of 100 and 200 mg/l, respectively. The enzyme activity was measured using NADH as a substrate. Fourier transform infrared spectroscopy (FT-IR) analysis was confirmed that the transformation of azo linkage could be transformed into N2 or NH3 or incorporated into complete biomass. Breaking down of dye molecules to various metabolites (such as aniline, naphthalene-1,4-diamine, 3-aminobenzenesulfonic acid, naphthalene-1-sulfonic acid, 8-aminonaphthalene-1-sulfonic acid, 5,8-diaminonaphthalene-1-sulfonic acid) was confirmed by gas chromatography and mass spectra (GC-MS) and mass (electrospray ionization (ESI)) spectra analysis. The treated wastewater could be reused for dyeing operation in the leather processing, and the properties of produced leather were evaluated by conventional methods that revealed to have improved dye penetration into the grain layer of experimental leather sample and resulted in high levelness of dyeing, which helps to obtain the desired smoothness and soft leather properties.

  12. Isolation and Characterization of Paracoccus sp. GSM2 Capable of Degrading Textile Azo Dye Reactive Violet 5

    Directory of Open Access Journals (Sweden)

    Mallikarjun C. Bheemaraddi

    2014-01-01

    Full Text Available A potential bacterial strain GSM2, capable of degrading an azo dye Reactive Violet 5 as a sole source of carbon, was isolated from textile mill effluent from Solapur, India. The 16S rDNA sequence and phenotypic characteristics indicated an isolated organism as Paracoccus sp. GSM2. This strain exhibited complete decolorization of Reactive Violet 5 (100 mg/L within 16 h, while maximally it could decolorize 800 mg/L of dye within 38 h with 73% decolorization under static condition. For color removal, the most suitable pH and temperature were pH 6.0–9.0 and 25–40°C, respectively. The isolate was able to decolorize more than 70% of five structurally different azo dyes within 38 h. The isolate is salt tolerant as it can bring out more than 90% decolorization up to a salt concentration of 2% (w/v. UV-Visible absorption spectra before and after decolorization suggested that decolorization was due to biodegradation and was further confirmed by FT-IR spectroscopy. Overall results indicate the effectiveness of the strain GSM2 explored for the treatment of textile industry effluents containing various azo dyes. To our knowledge, this could be the first report on biodegradation of Reactive Violet 5 by Paracoccus sp. GSM2.

  13. Immobilized laccase mediated dye decolorization and transformation pathway of azo dye acid red 27.

    Science.gov (United States)

    Chhabra, Meenu; Mishra, Saroj; Sreekrishnan, Trichur Ramaswamy

    2015-01-01

    Laccases have good potential as bioremediating agents and can be used continuously in the immobilized form like many other enzymes. In the present study, laccase from Cyathus bulleri was immobilized by entrapment in Poly Vinyl Alcohol (PVA) beads cross-linked with either nitrate or boric acid. Immobilized laccase was used for dye decolorization in both batch and continuous mode employing a packed bed column. The products of degradation of dye Acid Red 27 were identified by LC MS/MS analysis. The method led to very effective (90%) laccase immobilization and also imparted significant stability to the enzyme (more than 70% after 5 months of storage at 4°C). In batch decolorization, 90-95% decolorization was achieved of the simulated dye effluent for up to 10-20 cycles. Continuous decolorization in a packed bed bioreactor led to nearly 90% decolorization for up to 5 days. The immobilized laccase was also effective in decolorization and degradation of Acid Red 27 in the presence of a mediator. Four products of degradation were identified by LC-MS/MS analysis. The immobilized laccase in PVA-nitrate was concluded to be an effective agent in treatment of textile dye effluents.

  14. Optimization of integrated chemical-biological degradation of a reactive azo dye using response surface methodology

    Energy Technology Data Exchange (ETDEWEB)

    Sudarjanto, Gatut [Advanced Wastewater Management Centre, The University of Queensland, Qld 4072 (Australia); Keller-Lehmann, Beatrice [Advanced Wastewater Management Centre, The University of Queensland, Qld 4072 (Australia); Keller, Jurg [Advanced Wastewater Management Centre, The University of Queensland, Qld 4072 (Australia)]. E-mail: j.keller@awmc.uq.edu.au

    2006-11-02

    The integrated chemical-biological degradation combining advanced oxidation by UV/H{sub 2}O{sub 2} followed by aerobic biodegradation was used to degrade C.I. Reactive Azo Red 195A, commonly used in the textile industry in Australia. An experimental design based on the response surface method was applied to evaluate the interactive effects of influencing factors (UV irradiation time, initial hydrogen peroxide dosage and recirculation ratio of the system) on decolourisation efficiency and optimizing the operating conditions of the treatment process. The effects were determined by the measurement of dye concentration and soluble chemical oxygen demand (S-COD). The results showed that the dye and S-COD removal were affected by all factors individually and interactively. Maximal colour degradation performance was predicted, and experimentally validated, with no recirculation, 30 min UV irradiation and 500 mg H{sub 2}O{sub 2}/L. The model predictions for colour removal, based on a three-factor/five-level Box-Wilson central composite design and the response surface method analysis, were found to be very close to additional experimental results obtained under near optimal conditions. This demonstrates the benefits of this approach in achieving good predictions while minimising the number of experiments required.

  15. Optimization of integrated chemical-biological degradation of a reactive azo dye using response surface methodology

    International Nuclear Information System (INIS)

    Sudarjanto, Gatut; Keller-Lehmann, Beatrice; Keller, Jurg

    2006-01-01

    The integrated chemical-biological degradation combining advanced oxidation by UV/H 2 O 2 followed by aerobic biodegradation was used to degrade C.I. Reactive Azo Red 195A, commonly used in the textile industry in Australia. An experimental design based on the response surface method was applied to evaluate the interactive effects of influencing factors (UV irradiation time, initial hydrogen peroxide dosage and recirculation ratio of the system) on decolourisation efficiency and optimizing the operating conditions of the treatment process. The effects were determined by the measurement of dye concentration and soluble chemical oxygen demand (S-COD). The results showed that the dye and S-COD removal were affected by all factors individually and interactively. Maximal colour degradation performance was predicted, and experimentally validated, with no recirculation, 30 min UV irradiation and 500 mg H 2 O 2 /L. The model predictions for colour removal, based on a three-factor/five-level Box-Wilson central composite design and the response surface method analysis, were found to be very close to additional experimental results obtained under near optimal conditions. This demonstrates the benefits of this approach in achieving good predictions while minimising the number of experiments required

  16. Azo dyes decomposition on new nitrogen-modified anatase TiO2 with high adsorptivity

    International Nuclear Information System (INIS)

    Janus, M.; Choina, J.; Morawski, A.W.

    2009-01-01

    New vis active photocatalyst was obtained by the modification of commercial anatase TiO 2 (Police, Poland) in pressure reactor in an ammonia water atmosphere at 100 o C for 4 h. The photocatalytic activity of new material was tested during three azo dyes decomposition: monoazo (Reactive Read), diazo (Reactive Black) and poliazodye (Direct Green). Obtained photocatalyst had new bands at 1430-1440 cm -1 attributed to the bending vibrations of NH 4 + and at 1535 cm -1 associated with NH 2 groups or NO 2 and NO. UV-vis/DR spectra of photocatalyst had also insignificant decrease in visible region. Fluorescence technique was used for studying the amount of hydroxyl radicals produced on TiO 2 surface during visible light irradiation. The hydroxyl radicals produced react with coumarin present in the solution to form 7-hydroxycoumarin which has fluorescent capacity. Photocatalytic activity of modified TiO 2 was compared with commercial titanium dioxide P25 (Degussa, Germany). The photocatalytic activity of TiO 2 /N was higher than that of unmodified material and P25 under visible light irradiation. The ability for dye adsorption (Reactive Red) on photocatalyst surface was also tested. Unmodified TiO 2 and P25 has isotherm of adsorption by Freundlich model, and nitrogen-modified TiO 2 by Langmuir model. The presence of nitrogen at the surface of TiO 2 significantly increased adsorption capacity of TiO 2 as well as OH· radicals formation under visible radiation.

  17. Fenton oxidative decolorization of the azo dye Direct Blue 15 in aqueous solution

    DEFF Research Database (Denmark)

    Sun, Jian-Hui; Shi, Shao-Hui; Lee, Yi-Fan

    2009-01-01

    In this paper, the application of Fenton oxidation process for the decolorization of an azo dye Direct Blue 15 (DB15) in aqueous solution was investigated. The effect of initial pH, dosage of H2O2, H2O2/Fe2+ and H2O2/dye ratios and the reaction temperature on the decolorization efficiency...... = 60: 1 and temperature = 30 degrees C. Under the optimal conditions, 4.7 x 10(-5) mol/L of the DB15 aqueous solution can be completely decolorized by Fenton oxidation within 50-min reaction time and the decolorization kinetic rate constant k was determined as 0.1694 min(-1). Additionally increasing...... the reaction temperature from 20 to 40 degrees C showed a positive effect on the decolorization efficiency of DB15. The present study can provide guidance to relational industry operators and planners to effectively treat the DB15 contaminated wastewater by Fenton oxidation process. (C) 2009 Elsevier B. V. All...

  18. Synthesis and Evaluation of Changes Induced by Solvent and Substituent in Electronic Absorption Spectra of New Azo Disperse Dyes Containig Barbiturate Ring

    Directory of Open Access Journals (Sweden)

    Hooshang Hamidian

    2013-01-01

    Full Text Available Six azo disperse dyes were prepared by diazotizing 4-amino hippuric acid and coupled with barbituric acid and 2-thiobarbituric acid. Then, the products were reacted with aromatic aldehyde, sodium acetate, and acetic anhydride, and oxazolone derivatives were formed. Characterization of the dyes was carried out by using UV-Vis, FT-IR, 1H NMR and 13C NMR, and mass spectroscopic techniques. The solvatochromic behavior of azo disperse dyes was evaluated in various solvents. The effects of substituents of aromatic aldehyde, barbiturate, and thiobarbiturate ring on the color of dyes were investigated.

  19. DECOLORIZATION OF AZO DYES AND MINERALIZATION OF PHENANTHRENE BY TRAMETES SP. AS03 ISOLATED FROM INDONESIAN MANGROVE FOREST

    Directory of Open Access Journals (Sweden)

    Asep Hidayat

    2014-04-01

    Full Text Available Textile industry contributes the most disposals of synthetic dyes, and about 40% of textile dyes has been generating high amount of colored wastewater. Polycyclic aromatic hydrocarbons (PAHs, such as phenanthrene, is a group of organic compounds, that structurally comprised of two or more benzene rings, which persist in air, water, and soil. The organic pollutants of dyes and PAHs have adversely effects the food chain and are potentially toxic, mutagenic, and carcinogenic to the environment. The objective of this research is to screen and investigate the potential fungus from mangrove forest to degrade azo dyes and phenanthrene.  In this study, fungi were collected from mangrove forest in Riau Province – Sumatra – Indonesia. Previously, Trametes sp. AS03 is one of the fungi isolated from mangrove forest in Riau Province, that was able to decolorize Remazol Brilliant Blue R (RBBR. The capability of Trametes sp. AS03 to decolorize four azo dyes, Remazol B. Violet (V5, Levafix Orange E3GA (Or64, Levafix B. Red E-6BA (R159, and Sumifix S. Scarlet 2GF (R222, were further evaluated. The result shows that Trametes sp. AS03 decolorized 91, 60, 48, and 31 of V5, R222, R159, and Or64, respectively. By showing its capability to decolorize some of the dyes, Trametes sp. AS03 was used to break down phenanthrene. AS03 degraded more than 70% of phenanthrene in 15 days.

  20. BF3.SiO2: an efficient catalyst for the synthesis of azo dyes at room temperature

    Directory of Open Access Journals (Sweden)

    Bi Bi Fatemeh Mirjalili

    2012-07-01

    Full Text Available A rapid one-pot method has been developed for the synthesis of azo dyes via ‎sequential diazotization–diazo coupling of aromatic amines with coupling agents at room ‎temperature in the presence of BF3.SiO2 as acidic catalyst. The obtained aryl diazonium salts bearing silica supported boron tri-flouride counter ion‎ was sufficiently stable to be kept at room ‎temperature in the dry state.‎

  1. Synthesis and antibacterial activity of novel Pyrazolo [3, 4-B] quinoline based heterocyclic azo compounds and their dyeing performance

    International Nuclear Information System (INIS)

    Thaokar, Sanjay F.; Patel, Dinesh M.; Patel, Manish P.; Patel, Ranjan G.

    2007-01-01

    3-Amino-6-methyl-1H- pyrazolo [3, 4-B] quinoline was synthesized in good yield. Monoazo compounds were prepared using this intermediate as diazo component with various heterocyclic coupling components. All the azo compounds were characterized by their percentage yield, melting point, elemental analysis, UV-visible spectra, IR-spectra and dyeing performance on nylon and polyester fibres and by their antibacterial activity against gram positive and gram negative bacteria. (author)

  2. Strong guided mode resonant local field enhanced visible harmonic generation in an azo-polymer resonant waveguide grating.

    Science.gov (United States)

    Lin, Jian Hung; Tseng, Chun-Yen; Lee, Ching-Ting; Young, Jeff F; Kan, Hung-Chih; Hsu, Chia Chen

    2014-02-10

    Guided mode resonance (GMR) enhanced second- and third-harmonic generation (SHG and THG) is demonstrated in an azo-polymer resonant waveguide grating (RWG), comprised of a poled azo-polymer layer on top of a textured SU8 substrate with a thin intervening layer of TiO2. Strong SHG and THG outputs are observed by matching either in-coming fundamental- or out-going harmonic-wavelength to the GMR wavelengths of the azo-polymer RWG. Without the azo-polymer coating, pure TiO2 RWGs, do not generate any detectable SHG using a fundamental beam peak intensity of 2 MW/cm(2). Without the textured TiO2 layer, a planar poled azo-polymer layer results in 3650 times less SHG than the full nonlinear RWG structure under identical excitation conditions. Rigorous coupled-wave analysis calculations confirm that this enhancement of the nonlinear conversion is due to strong local electric fields that are generated at the interfaces of the TiO2 and azo-polymer layers when the RWG is excited at resonant wavelengths associated with both SHG and THG conversion processes.

  3. [Decolorization of the azo dye reactive red X-3B by an Al-Cu bimetallic system].

    Science.gov (United States)

    Fan, Jin-hong; Ma, Lu-ming; Wang, Hong-wu; Wu, De-li

    2008-06-01

    The decoloration mechanism and kinetics of the azo dye reactive red X-3B by an Al-Cu bimetallic system were investigated by measuring the dye removal, the TOC removal and the aniline concentration, and by adding EDTA as control experiments. The results showed the colority removal rate of X-3B reached 83% in the near neutral pH medium for 30 min and 96.4% for 120 min, in which, about 34% was due to the X-3B reduced to aniline, and about 20% and 30% was due to the flocculating of aluminum ions and surface adsorption of aluminum-fillings respectively. The decolorization of dyeing wastewater is a gradual reaction process, which first adsorbs a large number of dyeing ingredients and then carries out inner electrolysis reduction, improved effectively by the flocculating action of aluminum ions. The decolorization reaction appears to be a pseudo first-order reaction and increases with rising temperature.

  4. Colorful and transparent poly(vinyl alcohol) composite films filled with layered zinc hydroxide salts, intercalated with anionic orange azo dyes (methyl orange and orange II)

    International Nuclear Information System (INIS)

    Neves da Silva, Marlon Luiz; Marangoni, Rafael; Cursino, Ana Cristina Trindade; Schreiner, Wido Herwig; Wypych, Fernando

    2012-01-01

    Highlights: ► Zinc hydroxide salts were successfully intercalated with anionic orange azo dyes. ► The anionic dye was co-intercalated with hydrated chloride anions. ► The orange materials were used as fillers for poly(vinyl alcohol). ► Transparent, homogeneous, colorful PVA films were obtained by wet casting. ► Some composites stored at lower humidity exhibited improved mechanical properties. - Abstract: Layered zinc hydroxide salts (zinc LHS) were intercalated with anionic orange azo dyes, namely methyl orange (MO) and orange II (OII), and co-intercalated with hydrated chloride anions. After characterization by X-ray diffraction (XRD), thermal analysis (TGA/DTA), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), the materials were used as fillers for poly(vinyl alcohol) (PVA). Colorful transparent films were obtained by wet casting, revealing good dispersion of the material into the polymer. In the case of zinc LHS/OII, PVA was intercalated between the zinc LHS layers. Evaluation of the mechanical properties of the PVA composite films revealed that the layered colorful materials were able to increase the mechanical properties of the PVA films only when the films were stored under lower relative humidity. As expected, films with higher water content displayed reduced tensile strength and modulus because of the plasticizing effect of water. As for the films stored at 43% relative humidity, more pronounced improvement of modulus was observed for 1 and 4% zinc LHS/OII, and enhanced tensile strength was achieved for 0.5 and 1% zinc LHS/OII. This effect can be attributed to better dispersion of the layered filler and its better adhesion to the PVA matrix.

  5. Atomic-Layer-Deposited AZO Outperforms ITO in High-Efficiency Polymer Solar Cells

    KAUST Repository

    Kan, Zhipeng

    2018-05-11

    Tin-doped indium oxide (ITO) transparent conducting electrodes are widely used across the display industry, and are currently the cornerstone of photovoltaic device developments, taking a substantial share in the manufacturing cost of large-area modules. However, cost and supply considerations are set to limit the extensive use of indium for optoelectronic device applications and, in turn, alternative transparent conducting oxide (TCO) materials are required. In this report, we show that aluminum-doped zinc oxide (AZO) thin films grown by atomic layer deposition (ALD) are sufficiently conductive and transparent to outperform ITO as the cathode in inverted polymer solar cells. Reference polymer solar cells made with atomic-layer-deposited AZO cathodes, PCE10 as the polymer donor and PC71BM as the fullerene acceptor (model systems), reach power conversion efficiencies of ca. 10% (compared to ca. 9% with ITO-coated glass), without compromising other figures of merit. These ALD-grown AZO electrodes are promising for a wide range of optoelectronic device applications relying on TCOs.

  6. Atomic-Layer-Deposited AZO Outperforms ITO in High-Efficiency Polymer Solar Cells

    KAUST Repository

    Kan, Zhipeng; Wang, Zhenwei; Firdaus, Yuliar; Babics, Maxime; Alshareef, Husam N.; Beaujuge, Pierre

    2018-01-01

    Tin-doped indium oxide (ITO) transparent conducting electrodes are widely used across the display industry, and are currently the cornerstone of photovoltaic device developments, taking a substantial share in the manufacturing cost of large-area modules. However, cost and supply considerations are set to limit the extensive use of indium for optoelectronic device applications and, in turn, alternative transparent conducting oxide (TCO) materials are required. In this report, we show that aluminum-doped zinc oxide (AZO) thin films grown by atomic layer deposition (ALD) are sufficiently conductive and transparent to outperform ITO as the cathode in inverted polymer solar cells. Reference polymer solar cells made with atomic-layer-deposited AZO cathodes, PCE10 as the polymer donor and PC71BM as the fullerene acceptor (model systems), reach power conversion efficiencies of ca. 10% (compared to ca. 9% with ITO-coated glass), without compromising other figures of merit. These ALD-grown AZO electrodes are promising for a wide range of optoelectronic device applications relying on TCOs.

  7. Conducting polypyrrole films as a potential tool for electrochemical treatment of azo dyes in textile wastewaters

    Energy Technology Data Exchange (ETDEWEB)

    Haque, Md. Mominul [Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, NSW 2109 (Australia); Smith, Warren T. [Samadha Pacifica Pty Ltd, Woonona, NSW 2517 (Australia); Wong, Danny K.Y., E-mail: Danny.Wong@mq.edu.au [Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, NSW 2109 (Australia)

    2015-02-11

    Highlights: • Anion exchange property of polypyrrole films exploited in developing a treatment method for Acid Red 1. • An environmentally friendly treatment method for Acid Red 1 without generating any toxic by-products. • Acid Red 1 is anodically entrapped and cathodically liberated at polypyrrole films. • Analytical characteristics of Acid Red 1-entrapped polypyrrole films. - Abstract: In this paper, we demonstrate conducting polypyrrole films as a potential green technology for electrochemical treatment of azo dyes in wastewaters using Acid Red 1 as a model analyte. These films were synthesised by anodically polymerising pyrrole in the presence of Acid Red 1 as a supporting electrolyte. In this way, the anionic Acid Red 1 is electrostatically attracted to the cationic polypyrrole backbone formed to maintain electroneutrality, and is thus entrapped in the film. These Acid Red 1-entrapped polypyrrole films were characterised by electrochemical, microscopic and spectroscopic techniques. Based on a two-level factorial design, the solution pH, Acid Red 1 concentration and polymerisation duration were identified as significant parameters affecting the entrapment efficiency. The entrapment process will potentially aid in decolourising Acid Red 1-containing wastewaters. Similarly, in a cathodic process, electrons are supplied to neutralise the polypyrrole backbone, liberating Acid Red 1 into a solution. In this work, following an entrapment duration of 480 min in 2000 mg L{sup −1} Acid Red 1, we estimated 21% of the dye was liberated after a reduction period of 240 min. This allows the recovery of Acid Red 1 for recycling purposes. A distinctive advantage of this electrochemical Acid Red 1 treatment, compared to many other techniques, is that no known toxic by-products are generated in the treatment. Therefore, conducting polypyrrole films can potentially be applied as an environmentally friendly treatment method for textile effluents.

  8. Green synthesis of palladium nanoparticles with carboxymethyl cellulose for degradation of azo-dyes

    Energy Technology Data Exchange (ETDEWEB)

    Li, Gang; Li, Yun; Wang, Zhengdong; Liu, Huihong, E-mail: huihongliu@126.com

    2017-02-01

    Palladium nanoparticles (PdNPs) were synthesized through friendly environmental method using PdCl{sub 2} and carboxymethyl cellulose (CMC) in an aqueous solution (pH 6) at controlled water bath (80 °C) for 30 min. CMC functioned as both reducing and stabilizing agent. The characterization through high resolution-transmission electron microscopic (HRTEM) and X-ray Fluorescence Spectrometry (XRF) inferred that the as-synthesized PdNPs were spherical in shape with a face cubic crystal (FCC) structure. The results from dynamic light scattering (DLS) suggested the PdNPs had the narrow size distribution with an average size of 2.5 nm. The negative zeta potential (−52.6 mV) kept the as-synthesized PdNPs stable more than one year. The PdNPs showed the excellent catalytic activity by reducing degradation of azo-dyes, such as p-Aminoazobenzene, acid red 66, acid orange 7, scarlet 3G and reactive yellow 179, in the present of sodium borohydride. - Highlights: • Green synthesis of palladium nanoparticles using carboxymethyl cellulose. • The synthesis of palladium nanoparticles were performed easily. • Carboxymethyl cellulose acts as both reducing and stabilization agents. • The as-synthesized palladium nanoparticles show excellent catalytic activity.

  9. Decolorization of Mordant red 73 azo dye in water using H2O2/UV and photo-Fenton treatment.

    Science.gov (United States)

    Elmorsi, Taha M; Riyad, Yasser M; Mohamed, Zeinhom H; Abd El Bary, Hassan M H

    2010-02-15

    Decolorization of the Mordant red 73 (MR73) azo dye in water was investigated in laboratory-scale experiments using UV/H(2)O(2) and photo-Fenton treatments. Photodegradation experiments were carried out in a stirred batch photoreactor equipped with a low-pressure mercury lamp as UV source at 254 nm. The effect of operating parameters such as pH, [H(2)O(2)](,) [dye] and the presence of inorganic salts (NaNO(3), NaCl and Na(2)CO(3)) were also investigated. The results indicated that complete dye decolorization was obtained in less than 60 min under optimum conditions. Furthermore, results showed that dye degradation was dependent upon pH, [H(2)O(2)] and initial dye concentration. The presence of chloride ion led to large decreases in the photodegradation rate of MR73 while both nitrate and carbonate ions have a slight effect. The photo-Fenton treatment, in the presence of Fe powder as a source of Fe(2+) ions, was highly efficient and resulted in 99% decolorization of the dye in 15 min. Mineralization of MR73 dye was investigated by determining chemical oxygen demand (COD). In a 3h photoperiod "65%" of the dye was mineralized by the H(2)O(2)/UV process, while the photo-Fenton treatment was more efficient producing 85% mineralization over the same 3-h period.

  10. Transport behaviors of anionic azo dyes at interface between surfactant-modified flax shives and aqueous solution: Synchrotron infrared and adsorption studies

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wenxia [MOE Key Laboratory of Resources and Environmental Systems Optimization, Institute for Energy, Environment and Sustainability Research, UR-NCEPU, North China Electric Power University, Beijing, 102206 (China); Huang, Guohe, E-mail: huang@iseis.org [MOE Key Laboratory of Resources and Environmental Systems Optimization, Institute for Energy, Environment and Sustainability Research, UR-NCEPU, North China Electric Power University, Beijing, 102206 (China); An, Chunjiang; Xin, Xiaying [Institute for Energy, Environment and Sustainable Communities, University of Regina, Regina, S4S 0A2 (Canada); Zhang, Yan [MOE Key Laboratory of Resources and Environmental Systems Optimization, Institute for Energy, Environment and Sustainability Research, UR-NCEPU, North China Electric Power University, Beijing, 102206 (China); Liu, Xia [Canadian Light Source, Saskatoon, S7N 2V3 (Canada)

    2017-05-31

    Highlights: • Surfactant modified flax shives for removing anionic azo dyes. • The equilibrium and kinetic studies for the adsorption of anionic azo dyes. • The migration patterns of dye pollutants at flax shive-water interface. • New insights from synchrotron infrared-assisted characterization. • Potential as biomass adsorbent for the removal of dyes from wastewater. - Abstract: From the viewpoint of sustainability, biomass adsorbent has a high potential in pollution control and there is an emerging interest to investigate the behaviors of pollutants at the interface between biomass adsorbent and solution. This study investigated the performance of cetyltrimethylammonium bromide surfactant-modified flax shives (MFS) for removal of anionic azo dyes from aqueous solution. The equilibrium and kinetic analysis for the adsorption of Acid Orange 7 (AO-7), Acid Red 18 (AR-18) and Acid Black 1 (AB-1) on MFS were conducted. The surface of MFS was characterized by synchrotron infrared and SEM analysis. The absorbed amount of three anionic azo dyes varied with the change of adsorbent dosage, pH and ionic strength. The adsorption isotherm data well fit to the Langmuir model. The adsorption process followed the pseudo-second-order kinetics and the liquid film diffusion models. Thermodynamic studies indicated that the adsorption of three anionic azo dyes was spontaneous. The adsorption of AR-18 and AB-1 onto MFS was endothermic while the adsorption of AO-7 was exothermic. The results can help better understand the behaviors of organic pollutants at biomass adsorbent-water interface. They also present the potential of using MFS as a suitable adsorbent for the removal of anionic azo dyes from wastewater.

  11. Transport behaviors of anionic azo dyes at interface between surfactant-modified flax shives and aqueous solution: Synchrotron infrared and adsorption studies

    International Nuclear Information System (INIS)

    Wang, Wenxia; Huang, Guohe; An, Chunjiang; Xin, Xiaying; Zhang, Yan; Liu, Xia

    2017-01-01

    Highlights: • Surfactant modified flax shives for removing anionic azo dyes. • The equilibrium and kinetic studies for the adsorption of anionic azo dyes. • The migration patterns of dye pollutants at flax shive-water interface. • New insights from synchrotron infrared-assisted characterization. • Potential as biomass adsorbent for the removal of dyes from wastewater. - Abstract: From the viewpoint of sustainability, biomass adsorbent has a high potential in pollution control and there is an emerging interest to investigate the behaviors of pollutants at the interface between biomass adsorbent and solution. This study investigated the performance of cetyltrimethylammonium bromide surfactant-modified flax shives (MFS) for removal of anionic azo dyes from aqueous solution. The equilibrium and kinetic analysis for the adsorption of Acid Orange 7 (AO-7), Acid Red 18 (AR-18) and Acid Black 1 (AB-1) on MFS were conducted. The surface of MFS was characterized by synchrotron infrared and SEM analysis. The absorbed amount of three anionic azo dyes varied with the change of adsorbent dosage, pH and ionic strength. The adsorption isotherm data well fit to the Langmuir model. The adsorption process followed the pseudo-second-order kinetics and the liquid film diffusion models. Thermodynamic studies indicated that the adsorption of three anionic azo dyes was spontaneous. The adsorption of AR-18 and AB-1 onto MFS was endothermic while the adsorption of AO-7 was exothermic. The results can help better understand the behaviors of organic pollutants at biomass adsorbent-water interface. They also present the potential of using MFS as a suitable adsorbent for the removal of anionic azo dyes from wastewater.

  12. FACTORS AFFECTING THE REMOVAL OF A BASIC AND AN AZO DYE FROM ARTIFICIAL SOLUTIONS BY ADSORPTION USING ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    H Albroomi

    2014-10-01

    Full Text Available Decolourisation of wastewater, particularly from textile industries, is one of the major environmental concerns these days. Current methods for removing dyes from wastewater are costly and cannot effectively be used to treat wide range of such wastewater. This work describes the use of commercial available granular activated carbon (GAC as an efficient adsorbent material for dyes removal. Aqueous solutions of various basic dye Methylene Blue (MB and azo-dye Tartrazine with concentrations 5-20 mg l–1 and 10-100 mg l–1, respectively, were shaken with certain amount of GAC to determine the adsorption capacity and removal efficiencies. The effects of adsorbent dose, initial pH, initial dye concentration, agitation speed and contact time on dyes removal efficiencies have been studied. Maximum dye concentration was removed from the solution within 60-90 min after the beginning of every experiment. Adsorption parameters were found to fit well into Langmuir and Freundlich adsorption isotherms models with correlation coefficient (R2 > 0.99 in the concentration range of MB and TZ studied.

  13. Spectroscopic and theoretical study of the "azo"-dye E124 in condensate phase: evidence of a dominant hydrazo form.

    Science.gov (United States)

    Almeida, Mariana R; Stephani, Rodrigo; Dos Santos, Hélio F; de Oliveira, Luiz Fernando C

    2010-01-14

    Spectroscopic techniques, including Raman, IR, UV/vis, and NMR were used to characterize the samples of the azo dye Ponceau 4R (also known as E124, New Coccine; Cochineal Red; C.I. no. 16255; Food Red No. 102), which is 1,3-naphthalenedisulfonic acid, 7-hydroxy-8-[(4-sulfo-1-naphthalenyl) azo] trisodium salt in aqueous solution and solid state. In addition, first principle calculations were carried out for the azo (OH) and hydrazo (NH) tautomers in order to assist in the assignment of the experimental data. The two intense bands observed in the UV/vis spectrum, centered at 332 and 507 nm, can be compared to the calculated values at 296 and 474 nm for azo and 315 and 500 nm for hydrazo isomer, with the latter in closer agreement to the experiment. The Raman spectrum is quite sensitive to tautomeric equilibrium; in solid state and aqueous solution, three bands were observed around 1574, 1515, and 1364 cm(-1), assigned to mixed modes including deltaNH + betaCH + nuCC, deltaNH + nuC horizontal lineO + nuC horizontal lineN + betaCH and nuCC vibrations, respectively. These assignments are predicted only for the NH species centered at 1606, 1554, and 1375 cm(-1). The calculated Raman spectrum for the azo (OH) tautomer showed two strong bands at 1468 (nuN = N + deltaOH) and 1324 cm(-1) (nuCC + nuC-N), which were not obtained experimentally. The (13)C NMR spectrum showed a very characteristic peak at 192 ppm assigned to the carbon bound to oxygen in the naphthol ring; the predicted values were 165 ppm for OH and 187 for NH isomer, supporting once again the predominance of NH species in solution. Therefore, all of the experimental and theoretical results strongly suggest the food dye Ponceau 4R or E124 has a major contribution of the hydrazo structure instead of the azo form as the most abundant in condensate phase.

  14. Efficient degradation of Azo dyes by a newly isolated fungus Trichoderma tomentosum under non-sterile conditions.

    Science.gov (United States)

    He, Xiao-Ling; Song, Chao; Li, Yuan-Yuan; Wang, Ning; Xu, Lei; Han, Xin; Wei, Dong-Sheng

    2018-04-15

    A fast-growing fungus with remarkable ability to degrade several azo dyes under non-sterile conditions was isolated and identified. This fungus was identified as Trichoderma tomentosum. Textile effluent of ten-fold dilution could be decolorized by 94.9% within 72h before optimization. Acid Red 3R model wastewater with a concentration of 85.5mgL -1 could be decolorized by 99.2% within the same time after optimization. High-level of manganese peroxidase and low-level of lignin peroxidase activities were detected during the process of decolorization from the culture supernatant, indicating the possible involvement of two enzymes in azo dye decolorization. No aromatic amine products were detected from the degradation products of Acid Red 3R by gas chromatography-mass spectrometry (GC/MS) analysis, indicating the possible involvement of a special symmetrical oxidative degradation pathway. Phytotoxicity assay confirmed the lower toxicity toward the test plant seeds of the degradation products when compared to the original dye. Copyright © 2017 Elsevier Inc. All rights reserved.

  15. Photocatalytic degradation of an azo-dye on TiO2/activated carbon composite material.

    Science.gov (United States)

    Andriantsiferana, C; Mohamed, E F; Delmas, H

    2014-01-01

    A sequential adsorption/photocatalytic regeneration process to remove tartrazine, an azo-dye in aqueous solution, has been investigated. The aim ofthis work was to compare the effectiveness of an adsorbent/photocatalyst composite-TiO2 deposited onto activated carbon (AC) - and a simple mixture of powders of TiO2 and AC in same proportion. The composite was an innovative material as the photocatalyst, TiO2, was deposited on the porous surface ofa microporous-AC using metal-organic chemical vapour deposition in fluidized bed. The sequential process was composed of two-batch step cycles: every cycle alternated a step of adsorption and a step of photocatalytic oxidation under ultra-violet (365 nm), at 25 degreeC and atmospheric pressure. Both steps, adsorption and photocatalytic oxidation, have been investigated during four cycles. For both materials, the cumulated amounts adsorbed during four cycles corresponded to nearly twice the maximum adsorption capacities qmax proving the photocatalytic oxidation to regenerate the adsorbent. Concerning photocatalytic oxidation, the degree of mineralization was higher with the TiO2/AC composite: for each cycle, the value of the total organic carbon removal was 25% higher than that obtained with the mixture powder. These better photocatalytic performances involved better regeneration than higher adsorbed amounts for cycles 2, 3 and 4. Better performances with this promising material - TiO2 deposited onto AC - compared with TiO2 powder could be explained by the vicinity of photocatalytic and AC adsorption sites.

  16. Effect of an azo dye (DR1) on the dielectric parameters of a nematic liquid crystal system

    International Nuclear Information System (INIS)

    Ozder, S.; Okutan, M.; Koeysal, O.; Goektas, H.; San, S.E.

    2007-01-01

    The dielectric parameters and relaxation properties of azo dye (DR1) doped E7 and pure E7 liquid crystal (LC) have been investigated in a wide frequency range of 10 k-10 MHz through the dielectric spectroscopy method at room temperature. Dielectric anisotropy (Δε) property of the LC changes from the positive type to negative type and dielectric anisotropy values decrease with doping of DR1. The relaxation frequency f r of E7 and E7/DR1 LC was calculated by means of Cole-Cole plots. Influence of bias voltage on the dielectric parameters has also been investigated

  17. Effect of addition of heavy metal ion on decolouration and degradation of azo dye in aqueous solution by gamma irradiation combined with ozone

    International Nuclear Information System (INIS)

    Lee, M.J.; Jin, J.H.; Nho, Y.C.; Arai, H.

    1998-01-01

    In decomposition of azo dyes solution by simultaneous application of gamma-ray and ozone treatment, the effect of addition of heavy metal ion upon decolouration and decomposition was studied. Cupric ion was used as a heavy metal ion. For the aqueous solution with and without addition of cupric ion, the degree of decolouration of 552 nm, the changes of pH, the reduction of TOC and BOD were measured as function of dose under condition of fixed concentration of ozone. It appeared that the addition of cupric ion played a positive role in decomposition of azo dye solution, but played a negative role in decolouration

  18. Decolorization and detoxification of Synozol red HF-6BN azo dye, by Aspergillus niger and Nigrospora sp

    Directory of Open Access Journals (Sweden)

    Sidra Ilyas

    2013-01-01

    Full Text Available In the present investigation the fungi, Aspergillus niger and Nigrospora sp. were employed for decolorization of Synazol red HF-6BN. Decolorization study showed that Aspergillus niger and Nigrospora sp. were able to decolorize 88% and 96% Synazol red 6BN, respectively, in 24 days. It was also studied that 86% and 90% Synazol red containing of dye effluent was decolorized by Aspergillus niger and Nigrospora sp. after 28 days of incubation at room temperature. A fungal-based protein with relative molecular mass of 70 kDa was partially purified and examined for enzymatic characteristics. The enzyme exhibited highest activity at temperature ranging from 40-50[degree sign]C and at pH=6.0. The enzyme activity was enhanced in the presence of metal cations. High performance liquid chromatography analysis confirmed that these fungal strains are capable to degrade Synazol red dye into metabolites. No zones of inhibition on agar plates and growth of Vigna radiata in the presence of dye extracted sample, indicated that the fungal degraded dye metabolites are nontoxic to beneficial micro-flora and plant growth. Aspergillus niger and Nigrospora sp. have promising potential in color removal from textile wastewater-containing azo dyes.

  19. Conductivity of oriented bis-azo polymer films

    DEFF Research Database (Denmark)

    Apitz, D.; Bertram, R.P.; Benter, N.

    2006-01-01

    The conductivity properties of electro-optic photoaddressable, dense bis-ozo chromophore polymer films are investigated by using samples corona poled at various temperatures. A dielectric spectrometer is applied to measure the frequency dependence of the conductivity at different temperatures...... before and after heating the material to above the glass transition temperature. The results show that the orientation of the chromophores changes the charge-carrier mobility. Ionic conductivity dominates in a more disordered configuration of the material, while the competing process of hole hopping...... takes over as a transition to a liquid-crystalline phase occurs when the material is heated to much higher than the gloss transition temperature. Such micro-crystallization strongly enhances the conductivity....

  20. Deciphering effects of functional groups and electron density on azo dyes degradation by graphene loaded TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Qian [College of Chemical Engineering, HuaQiao University, Xiamen 361021 (China); Liang, Xiao [School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093 (China); Chen, Bor-Yann [Department of Chemical and Materials Engineering, National I-Lan University, 26047, Taiwan (China); Chang, Chang-Tang, E-mail: ctchang@niu.edu.tw [Department of Environmental Engineering, National I-Lan University, 26047, Taiwan (China)

    2015-12-01

    Highlights: • The degradation pathways of RB5, RB171 and RR198 have been identified. • The favorable bond to be broken under photo degradation was deciphered in this research. • The breakages of the bonds were due to the electron density changes around the bonds. • The hydroxyl radicals as the main oxidized species were confirmed by positive hole trapper and ESR. - Abstract: This study tended to decipher the mechanism of photo degradation of azo dyes, which bond was favorable to be broken for application of wastewater decolorization. That is, from chemical structure perspective, the critical substituents to affect electron donor/acceptor for dye degradation would be identified in this research. The model reactive blacks (RB5), reactive blue 171 (RB171) and reactive red 198 (RR198) were degraded by graphene loaded TiO{sub 2}, indicating how the electron withdrawing and releasing groups affect azo dye degradability. The byproducts and intermediate products were analyzed by ultraviolet–visible spectroscopy (UV–vis), gas chromatography–mass spectrometry (GC–MS) and ion chromatography (IC). Furthermore, the radicals involved in the reaction were found by electron paramagnetic resonance (ESR) to confirm the main oxidized species of hydroxyl radicals rather than the light generated positive holes. The finding revealed that the breakages of the bonds were due to the electron density changes around the bonds. This principle can be applicable not only for RB5 degradation, but also for reactive blue 171 (RB171), reactive red 198 (RR198) and some other textile dyes.

  1. Time-dependent efficiency measurements of polymer solar cells with dye additives: unexpected initial increase of efficiency

    Science.gov (United States)

    Bandaccari, Kyle J.; Chesmore, Grace E.; Bugaj, Mitchel; Valverde, Parisa Tajalli-Tehrani; Barber, Richard P.; McNelis, Brian J.

    2018-04-01

    We report the effects of the addition of two azo-dye additives on the time-dependent efficiency of polymer solar cells. Although the maximum efficiencies of devices containing different amounts of dye do not vary greatly over the selected concentration range, the time dependence results reveal a surprising initial increase in efficiency in some samples. We observe this effect to be correlated with a leakage current, although a specific mechanism is not yet identified. We also present the measured lifetimes of these solar cells, and find that variations in dye concentrations produce a small effect at most. Characterization of the bulk heterojunction layer (active layer) morphology using atomic-force microscope (AFM) imaging reveals reordering patterns which suggest that the primary effects of the dyes arise via structural, not absorptive, characteristics.

  2. Sensitive spectrophotometric determination of aceclofenac following azo dye formation with 4-carboxyl-2,6-dinitrobenzene diazonium ion.

    Science.gov (United States)

    Aderibigbe, Segun A; Adegoke, Olajire A; Idowu, Olakunle S; Olaleye, Sefiu O

    2012-01-01

    The study is a description of a sensitive spectrophotometric determination of aceclofenac following azo dye formation with 4-carboxyl-2,6-dinitrobenzenediazonium ion (CDNBD). Spot test and thin layer chromatography revealed the formation of a new compound distinct from CDNBD and aceclofenac. Optimization studies established a reaction time of 5 min at 30 degrees C after vortex mixing the drug/CDNBD for 10 s. An absorption maximum of 430 nm was selected as analytical wavelength. A linear response was observed over 1.2-4.8 μg/mL of aceclofenac with a correlation coefficient of 0.9983 and the drug combined with CDNBD at stoichiometric ratio of 2 : 1. The method has a limit of detection of 0.403 μg/mL, limit of quantitation of 1.22 μg/mL and is reproducible over a three day assessment. The method gave Sandell's sensitivity of 3.279 ng/cm2. Intra- and inter-day accuracies (in terms of errors) were less than 6% while precisions were of the order of 0.03-1.89% (RSD). The developed spectrophotometric method is of equivalent accuracy (p > 0.05) with British Pharmacopoeia, 2010 potentiometric method. It has the advantages of speed, simplicity, sensitivity and more affordable instrumentation and could found application as a rapid and sensitive analytical method of aceclofenac. It is the first described method by azo dye derivatization for the analysis of aceclofenac in bulk samples and dosage forms.

  3. Efficient azo dye decolorization in a continuous stirred tank reactor (CSTR) with built-in bioelectrochemical system.

    Science.gov (United States)

    Cui, Min-Hua; Cui, Dan; Gao, Lei; Cheng, Hao-Yi; Wang, Ai-Jie

    2016-10-01

    A continuous stirred tank reactor with built-in bioelectrochemical system (CSTR-BES) was developed for azo dye Alizarin Yellow R (AYR) containing wastewater treatment. The decolorization efficiency (DE) of the CSTR-BES was 97.04±0.06% for 7h with sludge concentration of 3000mg/L and initial AYR concentration of 100mg/L, which was superior to that of the sole CSTR mode (open circuit: 54.87±4.34%) and the sole BES mode (without sludge addition: 91.37±0.44%). The effects of sludge concentration and sodium acetate (NaAc) concentration on azo dye decolorization were investigated. The highest DE of CSTR-BES for 4h was 87.66±2.93% with sludge concentration of 12,000mg/L, NaAc concentration of 2000mg/L and initial AYR concentration of 100mg/L. The results in this study indicated that CSTR-BES could be a practical strategy for upgrading conventional anaerobic facilities against refractory wastewater treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III.

    Science.gov (United States)

    Zanoni, Thalita Boldrin; Lizier, Thiago M; Assis, Marilda das Dores; Zanoni, Maria Valnice B; de Oliveira, Danielle Palma

    2013-07-01

    This work describes the mutagenic response of Sudan III, an adulterant food dye, using Salmonella typhimurium assay and the generation of hazardous aromatic amines after different oxidation methods of this azo dye. For that, we used metabolic activation by S9, catalytic oxidation by ironporphyrin and electrochemistry oxidation in order to simulate endogenous oxidation conditions. The oxidation reactions promoted discoloration from 65% to 95% of Sudan III at 1 × 10(-4)molL(-1) and generation of 7.6 × 10(-7)molL(-1) to 0.31 × 10(-4)molL(-1) of aniline, o-anisidine, 2-methoxi-5-methylaniline, 4-aminobiphenyl, 4,4'-oxydianiline; 4,4'-diaminodiphenylmethane and 2,6-dimethylaniline. The results were confirmed by LC-MS-MS experiments. We also correlate the mutagenic effects of Sudan III using S. typhimurium with the strain TA1535 in the presence of exogenous metabolic activation (S9) with the metabolization products of this compound. Our findings clearly indicate that aromatic amines are formed due to oxidative reactions that can be promoted by hepatic cells, after the ingestion of Sudan III. Considering that, the use of azo compounds as food dyestuffs should be carefully controlled. Copyright © 2013 Elsevier Ltd. All rights reserved.

  5. Evaluation of the adsorbent properties of a zeolite rock modified for the removal of the azo dyes as water pollutants

    International Nuclear Information System (INIS)

    Torres P, J.

    2005-01-01

    At the moment some investigations which make reference to the removal of dyes for diverse adsorbent materials; as well as the factors that influence in the sorption process, considering the type so much of dye as those characteristics of the adsorbent material. In this work were investigated those adsorbent properties of a zeolite rock coming from San Luis Potosi State for the removal of azo dyes, using as peculiar cases the Red 40 (Red Allura) and the Yellow 5 (Tartrazine); for it were determined kinetic parameters and the sorption isotherms, as well as the sorption mechanisms involved in each case, between the dyes and the zeolite rock. In this work also it was considered the characterization before and after to removal of color from the water, through advanced analytical techniques such as the scanning electron microscopy of high vacuum (SEM), elementary microanalysis (EDS) and X-ray diffraction (XRD). The experimental part of the work fundamentally consisted, in the conditioning with a NaCl solution and later on the modification with HDTMA-Br of the natural zeolite rock, for then to put it in contact with solutions of the dyes R-40 and A-5, varying so much the contact times as the concentrations; the quantification of sodium in the liquid phase after the modification of the zeolite rock to determine the capacity of external cation exchange (CICE) it was carried out by means of the atomic absorption spectroscopy technique (EAA), and the quantification of the surfactant and the dyes in the liquid phase, it was carried out by means of the UV-vis spectrophotometry technique. It was found that the kinetic model that better it describes the process of sorption of R-40 and A-5 for the modified zeolite rock with HDTMA-Br, leaving of monocomponent and bi component solutions, it is the pseudo- second order. Inside of the obtained results for the sorption isotherms, as much the dye R-40 as the dye A-5 its presented a better adjustment to the Langmuir model. In what refers

  6. Decolorization of the azo dye Acid Orange 51 by laccase produced in solid culture of a newly isolated Trametes trogii strain

    OpenAIRE

    Daâssi, Dalel; Zouari-Mechichi, Héla; Frikha, Fakher; Martínez, María Jesús; Nasri, M.; Mechichi, Tahar

    2013-01-01

    This study concerns the decolorization and detoxification of the azo dye Acid Orange 51 (AO51) by crude laccase from Trametes trogii produced in solid culture using sawdust as support media. A three-level Box?Behnken factorial design with four factors (enzyme concentration, 1-hydroxybenzotriazole (HBT) concentration, dye concentration and reaction time) combined with response surface methodology was applied to optimize AO51 decolorization. A mathematical model was developed showing the effect...

  7. Cancer risk assessment of azo dyes and aromatic amines from tattoo bands, folders of paper, toys, bed clothes, watch straps and ink

    NARCIS (Netherlands)

    Zeilmaker MJ; Kranen HJ van; Veen MP van; Janus J; LBM

    2000-01-01

    A quantitative assessment was performed to estimate the cancer risk to individuals using tattoo bands, folders of paper, toys, bed clothes, watch straps and ink which are coloured with azo dyes. In these products benzidine and the benzidine related amines o-anisidine, 2,4-toluenediamine,

  8. DMol3/COSMO-RS prediction of aqueous solubility and reactivity of selected Azo dyes: Effect of global orbital cut-off and COSMO segment variation

    CSIR Research Space (South Africa)

    Wahab, OO

    2018-01-01

    Full Text Available Aqueous solubility and reactivity of four azo dyes were investigated by DMol3/COSMO-RS calculation to examine the effects of global orbital cut-off and COSMO segment variation on the accuracies of theoretical solubility and reactivity. The studied...

  9. Kinetics of decolorization of azo dye by bipolar pulsed barrier discharge in a three-phase discharge plasma reactor.

    Science.gov (United States)

    Zhang, Ruobing; Zhang, Chi; Cheng, XingXin; Wang, Liming; Wu, Yan; Guan, Zhicheng

    2007-04-02

    Removal of amaranth, a commercial synthetic azo dye widely used in the dye and food industry, was examined as a possible remediation technology for treating dye-contaminated water. Effects of various parameters such as gas flow rate, solution conductivity, pulse repetition frequency, etc., on decolorization kinetics were investigated. Experimental results show that an aqueous solution of 24 mg/l dye is 81.24% decolorized following 30 min plasma treatment for a 50 kV voltage and 0.75 m(3)/h gas flow rate. Decolorization reaction of amaranth in the plasma reactor is a pseudo first order reaction. Rate constant (k) of decolorization increases quickly with increasing the applied voltage, pulse repetition frequency and the gas flow rate. However, when the applied voltage is beyond 50 kV and increases further, increase rate of k decreases. In addition, k decreases quickly when the solution conductivity increases from 200 to 1481 microS/cm. The decolorization reaction has a high rate constant (k=0.0269 min(-1)) when the solution pH is beyond 10. Rate constant k decreases with the decrease of pH and reaches minimum at a pH of about 5 (k(min)=0.01603 min(-1)), then increases to 0.02105 min(-1) when pH decreases to 3.07. About 15% of the initial TOC can be degraded only in about 120 min non-thermal plasma treatment.

  10. Biosurfactant production from Pseudomonas taiwanensis L1011 and its application in accelerating the chemical and biological decolorization of azo dyes.

    Science.gov (United States)

    Liu, Cong; You, Yanting; Zhao, Ruofei; Sun, Di; Zhang, Peng; Jiang, Jihong; Zhu, Aihua; Liu, Weijie

    2017-11-01

    Dye dispersion and the interaction efficiency between azoreductases and dye molecules are rate-limiting steps for the decolorization of azo dyes. In this study, a biosurfactant-producing strain, Pseudomonas taiwanensis L1011, was isolated from crude oil. To increase the yield of the biosurfactant BS-L1011 from P. taiwanensis L1011, culture conditions were optimized including temperature, initial pH, carbon source, nitrogen source and C/N ratio. A maximum yield of 1.12g/L of BS-L1011 was obtained using D-mannitol as carbon source and yeast extract/urea as compound nitrogen source with C/N ratio of 10/4, pH 7.0 and 28°C. BS-L1011 exhibited a low critical micelle concentration (CMC) of 10.5mg/L and was able to reduce the surface tension of water to 25.8±0.1 mN/m. BS-L1011 was stable over a wide range of temperatures, pH values and salt concentrations. The biosurfactant is reported for the first time to accelerate chemical decolorization of Congo red by sodium hypochlorite, and biological decolorization of Amaranth by Bacillus circulans BWL1061, thus showing a potential in the treatment of dyeing wastewater. Copyright © 2017 Elsevier Inc. All rights reserved.

  11. Kinetics of decolorization of azo dye by bipolar pulsed barrier discharge in a three-phase discharge plasma reactor

    International Nuclear Information System (INIS)

    Zhang Ruobing; Zhang Chi; Cheng Xingxin; Wang Liming; Wu Yan; Guan Zhicheng

    2007-01-01

    Removal of amaranth, a commercial synthetic azo dye widely used in the dye and food industry, was examined as a possible remediation technology for treating dye-contaminated water. Effects of various parameters such as gas flow rate, solution conductivity, pulse repetition frequency, etc., on decolorization kinetics were investigated. Experimental results show that an aqueous solution of 24 mg/l dye is 81.24% decolorized following 30 min plasma treatment for a 50 kV voltage and 0.75 m 3 /h gas flow rate. Decolorization reaction of amaranth in the plasma reactor is a pseudo first order reaction. Rate constant (k) of decolorization increases quickly with increasing the applied voltage, pulse repetition frequency and the gas flow rate. However, when the applied voltage is beyond 50 kV and increases further, increase rate of k decreases. In addition, k decreases quickly when the solution conductivity increases from 200 to 1481 μS/cm. The decolorization reaction has a high rate constant (k = 0.0269 min -1 ) when the solution pH is beyond 10. Rate constant k decreases with the decrease of pH and reaches minimum at a pH of about 5 (k min = 0.01603 min -1 ), then increases to 0.02105 min -1 when pH decreases to 3.07. About 15% of the initial TOC can be degraded only in about 120 min non-thermal plasma treatment

  12. Degradation efficiency and mechanism of azo dye RR2 by a novel ozone aerated internal micro-electrolysis filter.

    Science.gov (United States)

    Zhang, Xian-Bing; Dong, Wen-Yi; Sun, Fei-Yun; Yang, Wei; Dong, Jiao

    2014-07-15

    A newly designed ozone aerated internal micro-electrolysis filter (OIEF) was developed to investigate its degradation efficiencies and correlated reaction mechanisms of RR2 dye. Complete decolorization and 82% TOC removal efficiency were stably achieved in OIEF process. Based on the comprehensive experimental results, an empirical equation was proposed to illustrate the effects of initial dye concentration and ozone dosage rate on color removal. The results indicated that OIEF process could be operated at wide pH range without significant treatment efficiencies change, while the optimum pH for RR2 dye degradation was 9.0. There were 15, 8 and 6 kinds of identified intermediates during ozonation, IE and OIEF treatment processes, respectively. Less identified intermediates and their lower concentrations in OIEF may attribute to its rather excellent mineralization performance. It was found that ozonation, Fe(2+)/Fe(3+) catalyzed ozonation, the redox reactions of electro-reduction and electro-oxidation are the most important mechanisms in OIEF process. The catalytic effect of Fe(2+)/Fe(3+) would induce mutual conversion between dissolved Fe(2+) and Fe(3+), and then decrease the dissolution rate of ZVI. The excellent treatment performance proved that the OIEF process is one promising technology applied for reactive azo dyes and other refractory wastewater treatment. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Performance and microbial community structures of hydrolysis acidification process treating azo and anthraquinone dyes in different stages.

    Science.gov (United States)

    Liu, Na; Xie, Xuehui; Yang, Bo; Zhang, Qingyun; Yu, Chengzhi; Zheng, Xiulin; Xu, Leyi; Li, Ran; Liu, Jianshe

    2017-01-01

    In this study, performance of hydrolysis acidification process treating simulated dyeing wastewater containing azo and anthraquinone dyes in different stages was investigated. The decolorization ratio, COD Cr removal ratio, BOD 5 /COD Cr value, and volatile fatty acids (VFAs) production were almost better in stage 1 than that in stage 2. Fourier transform infrared spectroscopy (FTIR) and gas chromatography-mass spectrometry (GC-MS) confirmed the biodegradation of Reactive Black 5 (RB5) and Remazol Brilliant Blue R (RBBR) in hydrolysis acidification process. Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analyses revealed that significant difference of microbial community structures existed in stage 1 and 2. The dominant species in stage 1 was related to Bacteroidetes group, while the dominant species in stage 2 was related to Bacteroidetes and Firmicutes groups. From the results, it could be speculated that different dyes' structures might have significant influence on the existence and function of different bacterial species, which might supply information for bacteria screening and acclimation in the treatment of actual dyeing wastewater.

  14. Simultaneous Decolorization and Biohydrogen Production from Xylose by Klebsiella oxytoca GS-4-08 in the Presence of Azo Dyes with Sulfonate and Carboxyl Groups

    Science.gov (United States)

    Cao, Ming-yue; Wang, Peng-tao; Wang, Shi; Yue, Ying-rong; Yuan, Wen-duo; Qiao, Wei-chuan; Wang, Fei

    2017-01-01

    ABSTRACT Biohydrogen production from the pulp and paper effluent containing rich lignocellulosic material could be achieved by the fermentation process. Xylose, an important hemicellulose hydrolysis product, is used less efficiently as a substrate for biohydrogen production. Moreover, azo dyes are usually added to fabricate anticounterfeiting paper, which further increases the complexity of wastewater. This study reports that xylose could serve as the sole carbon source for a pure culture of Klebsiella oxytoca GS-4-08 to achieve simultaneous decolorization and biohydrogen production. With 2 g liter−1 of xylose as the substrate, a maximum xylose utilization rate (URxyl) and a hydrogen molar yield (HMY) of 93.99% and 0.259 mol of H2 mol of xylose−1, respectively, were obtained. Biohydrogen kinetics and electron equivalent (e− equiv) balance calculations indicated that methyl red (MR) penetrates and intracellularly inhibits both the pentose phosphate pathway and pyruvate fermentation pathway, while methyl orange (MO) acted independently of the glycolysis and biohydrogen pathway. The data demonstrate that biohydrogen pathways in the presence of azo dyes with sulfonate and carboxyl groups were different, but the azo dyes could be completely reduced during the biohydrogen production period in the presence of MO or MR. The feasibility of hydrogen production from industrial pulp and paper effluent by the strain if the xylose is sufficient was also proved and was not affected by toxic substances which usually exist in such wastewater, except for chlorophenol. This study offers a promising energy-recycling strategy for treating pulp and paper wastewaters, especially for those containing azo dyes. IMPORTANCE The pulp and paper industry is a major industry in many developing countries, and the global market of pulp and paper wastewater treatment is expected to increase by 60% between 2012 and 2020. Such wastewater contains large amounts of refractory contaminants, such

  15. Fe{sub 3}O{sub 4}@Nico-Ag magnetically recyclable nanocatalyst for azo dyes reduction

    Energy Technology Data Exchange (ETDEWEB)

    Kurtan, U., E-mail: ukurtan@fatih.edu.tr; Amir, Md.; Baykal, A.

    2016-02-15

    Graphical abstract: - Highlights: • Fe{sub 3}O{sub 4}@Nico@Ag magnetic recyclable nanocatalyst (MRC) is more effective for the reduction of azo dyes consisting of MB and MO. • It could be reused several times without significant loss in catalytic activity. • Fe{sub 3}O{sub 4}@Nico@Ag (MRCs) has been successively used for colour reduction of MO, MB, EY, RhB and their mixtures. - Abstract: In this study, we report the successful synthesis of Fe{sub 3}O{sub 4}@Nico-Ag nanocomposite as magnetically recyclable nanocatalyst (MRCs) via reflux process at 80 °C for 5 h followed by reduction of Ag{sup +}. FeCl{sub 3}·6H{sub 2}O, FeCl{sub 2}·4H{sub 2}O, AgNO{sub 3} as starting reactants and nicotinic acid as linker. The structure, morphology, thermal behaviour and magnetic properties of the product were characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive spectrometry (EDX), thermal gravimetry (TG) and vibrating sample magnetometry (VSM), respectively. The catalytic activity of product for various azo dyes such as methylene blue (MB), methyl orange (MO), Rhodamine B (RhB) and eosin Y (EY) and their double mixtures were studied. It was found that Fe{sub 3}O{sub 4}@Nico-Ag MRCs is an efficient catalyst and can also rapidly separated from the reaction medium using magnet without considerable loss in its catalytic activity and used several times. Fe{sub 3}O{sub 4}@Nico-Ag MRCs has potential for the treatment of industrial dye pollutants.

  16. Efeitos dos parâmetros operacionais na fotodegradação do azo corante direct red 23 na interface dióxido de titânio/água Effects of operational parameters on the photodegradation of direct red 23 azo dye at the titanium dioxide/water interface

    Directory of Open Access Journals (Sweden)

    Débora Nobile Clausen

    2007-01-01

    Full Text Available The decolorization and degradation of direct red 23 azo dye have been investigated in aqueous suspension of titanium dioxide under artificial irradiation. The effects of some operational parameters such as azo dye concentration, catalyst loading, and solution pH were investigated at 30.0 ºC and optimized values were obtained. The first-order kinetic model was used to discuss the results. The UV-Vis spectra changes showed that the azo dye sample, collected after 6 h irradiation, was 98% decolorized while the residual total carbon was 97.9% degraded, indicating simultaneous photodecolorization and degradation.

  17. Batch and fixed-bed adsorption of tartrazine azo-dye onto activated carbon prepared from apricot stones

    Science.gov (United States)

    Albroomi, H. I.; Elsayed, M. A.; Baraka, A.; Abdelmaged, M. A.

    2017-07-01

    This work describes the potential of utilizing prepared activated carbon from apricot stones as an efficient adsorbent material for tartrazine (TZ) azo-dye removal in a batch and dynamic adsorption system. The results revealed that activated carbons with well-developed surface area (774 m2/g) and pore volume (1.26 cm3/g) can be manufactured from apricot stones by H3PO4 activation. In batch experiments, effects of the parameters such as initial dye concentration and temperature on the removal of the dye were studied. Equilibrium was achieved in 120 min. Adsorption capacity was found to be dependent on the initial concentration of dye solution, and maximum adsorption was found to be 76 mg/g at 100 mg/L of TZ. The adsorption capacity at equilibrium ( q e) increased from 22.6 to 76 mg/g with an increase in the initial dye concentrations from 25 to 100 mg/L. The thermodynamic parameters such as change in free energy (Δ G 0), enthalpy (Δ H 0) and entropy (Δ S 0) were determined and the positive value of (Δ H) 78.1 (K J mol-1) revealed that adsorption efficiency increased with an increase in the process temperature. In fixed-bed column experiments, the effect of selected operating parameters such as bed depth, flow rate and initial dye concentration on the adsorption capacity was evaluated. Increase in bed height of adsorption columns leads to an extension of breakthrough point as well as the exhaustion time of adsorbent. However, the maximum adsorption capacities decrease with increases of flow rate. The breakthrough data fitted well to bed depth service time and Thomas models with high coefficient of determination, R 2 ≥ 94.

  18. Density functional theory study of adsorption geometries and electronic structures of azo-dye-based molecules on anatase TiO2 surface for dye-sensitized solar cell applications.

    Science.gov (United States)

    Prajongtat, Pongthep; Suramitr, Songwut; Nokbin, Somkiat; Nakajima, Koichi; Mitsuke, Koichiro; Hannongbua, Supa

    2017-09-01

    Structural and electronic properties of eight isolated azo dyes (ArNNAr', where Ar and Ar' denote the aryl groups containing benzene and naphthalene skeletons, respectively) were investigated by density functional theory (DFT) based on the B3LYP/6-31G(d,p) and TD-B3LYP/6-311G(d,p) methods The effect of methanol solvent on the structural and electronic properties of the azo dyes was elucidated by employing a polarizable continuum model (PCM). Then, the azo dyes adsorbed onto the anatase TiO 2 (101) slab surface through a carboxyl group. The geometries and electronic structures of the adsorption complexes were determined using periodic DFT based on the PWC/DNP method. The calculated adsorption energies indicate that the adsorbed dyes preferentially take configuration of the bidentate bridging rather than chelating or monodentate ester-type geometries. Furthermore, the azo compounds having two carboxyl groups are coordinated to the TiO 2 surface more preferentially through the carboxyl group connecting to the benzene skeleton than through that connecting to the naphthalene skeleton. The dihedral angles (Φ B-N ) between the benzene- and naphthalene-skeleton moieties are smaller than 10° for the adsorbed azo compounds containing one carboxyl group. In contrast, Φ B-N > 30° are obtained for the adsorbed azo compounds containing two carboxyl groups. The almost planar conformations of the former appear to strengthen both π-electrons conjugation and electronic coupling between low-lying unoccupied molecular orbitals of the azo dyes and the conduction band of TiO 2 . On the other hand, such coupling is very weak for the latter, leading to a shift of the Fermi level of TiO 2 in the lower-energy direction. The obtained results are useful to the design and synthesize novel azo-dye-based molecules that give rise to higher photovoltaic performances of the dye-sensitized solar cells. Copyright © 2017 Elsevier Inc. All rights reserved.

  19. Simultaneous determination of ten illegal azo dyes in feed by ultra-high performance liquid chromatography tandem mass spectrometry

    Directory of Open Access Journals (Sweden)

    Piątkowska Marta

    2017-09-01

    Full Text Available Introduction: The paper presents the method of simultaneous determination of 10 illegal azo dyes in feed by ultra-high performance liquid chromatography coupled with tandem mass spectrometry technique. Material and Methods: The dyes were extracted with hexane, evaporated to dryness, and analysed. Separation was achieved in 7 min in a gradient elution using acetonitrile (A and 0.1% formic acid (B as a mobile phase. Results: The validation results showed the repeatability of the method, which was evaluated at three levels (50, 500, and 5,000 μg/kg. All the matrix calibration curves for the working ranges were linear (R2 0.9904 to 1.0, the repeatability was between 2.1% and 24%, and recoveries ranged from 77.9% to 120%. The LOD and LOQ were at 1-2 and 5-10 μg/kg for different dyes, respectively. Furthermore, the method was applied in the homogeneity tests of the in-house prepared feed containing Sudan I at the levels of 0.5, 5, and 50 mg/kg. Conclusions: A sensitive, selective, and fast multiresidue method was successfully developed and validated. Its robustness was confirmed by the analysis of an experimental feed containing Sudan I.

  20. Aerobic sludge granulation for simultaneous anaerobic decolorization and aerobic aromatic amines mineralization for azo dye wastewater treatment.

    Science.gov (United States)

    Yan, Lawrence K Q; Fung, Ka Y; Ng, Ka M

    2018-06-01

    In this study, the capability of using aerobic granules to undergo simultaneous anaerobic decolorization and aerobic aromatic amines degradation was demonstrated for azo dye wastewater treatment. An integrated acclimation-granulation process was devised, with Mordant Orange 1 as the model pollutant. Performance tests were carried out in a batch column reactor to evaluate the effect of various operating parameters. The optimal condition was to use 1.0-1.7 mm (1.51 ± 0.33 mm) granules, 5 g/L biomass, and 4000 mg/L organics as nutrient; and supplement the wastewater with 1  mg/L dissolved oxygen. This led to a dye mineralization of 61 ± 2%, an anaerobic dye removal of 88 ± 1%, and an aerobic aromatic amines removal of 70 ± 3% within 48 h. This study showed that simultaneous anaerobic/aerobic process by aerobic granules could be a possible alternative to the conventional activated sludge process.

  1. Improved biodegradation of synthetic azo dye by horseradish peroxidase cross-linked on nano-composite support.

    Science.gov (United States)

    Sun, Huaiyan; Jin, Xinyu; Long, Nengbing; Zhang, Ruifeng

    2017-02-01

    A ZnO nanowires/macroporous SiO 2 composite was used as support to immobilize horseradish peroxidase (HRP) by in-situ cross-linking method. Using diethylene glycol diglycidyl ether (DDE) as a long-chained cross-linker, it was adsorbed on the surface of ZnO nanowires before reaction with HRPs, the resulted composite was quite different from the traditional cross-linking enzyme aggregates (CLEAs) on both structure and catalytic performance. The immobilized HRP showed high activity in the decolorization of azo dyes. The effect of various conditions such as the loading amount of HRP, solution pH, temperature, contact time and concentration of dye were optimized on the decolorization. The decolorization percentage of Acid Blue 113 and Acid black 10 BX reached as high as 95.4% and 90.3%, respectively. The immobilized HRP gave the highest decolorization rate under dye concentration as 50mg/L and reaction time of 35min. The immobilized HRP exhibited much better resistance to temperature and pH inactivation than free HRP. The storage stability and reusability were greatly improved through the immobilization, from the decolorization of Acid blue 113 it was found that 80.4% of initial efficiency retained after incubation at 4°C for 60 days, and that 79.4% of decolorization efficiency retained after 12 cycles reuse. Copyright © 2016 Elsevier B.V. All rights reserved.

  2. Rapid isolation of a facultative anaerobic electrochemically active bacterium capable of oxidizing acetate for electrogenesis and azo dyes reduction.

    Science.gov (United States)

    Shen, Nan; Yuan, Shi-Jie; Wu, Chao; Cheng, Yuan-Yuan; Song, Xiang-Ning; Li, Wen-Wei; Tong, Zhong-Hua; Yu, Han-Qing

    2014-05-01

    In this study, 27 strains of electrochemically active bacteria (EAB) were rapidly isolated and their capabilities of extracellular electron transfer were identified using a photometric method based on WO3 nanoclusters. These strains caused color change of WO3 from white to blue in a 24-well agar plate within 40 h. Most of the isolated EAB strains belonged to the genera of Aeromonas and Shewanella. One isolate, Pantoea agglomerans S5-44, was identified as an EAB that can utilize acetate as the carbon source to produce electricity and reduce azo dyes under anaerobic conditions. The results confirmed the capability of P. agglomerans S5-44 for extracellular electron transfer. The isolation of this acetate-utilizing, facultative EBA reveals the metabolic diversity of environmental bacteria. Such strains have great potential for environmental applications, especially at interfaces of aerobic and anaerobic environments, where acetate is the main available carbon source.

  3. Facile synthesis of 1-naphthol azo dyes with nano SiO2/HIO4 under solvent-free conditions

    Directory of Open Access Journals (Sweden)

    A.R. Pourali

    2013-09-01

    Full Text Available Nano-silica supported periodic acid (nano-SPIA has been utilized as a heterogeneous reagent for a highly efficient and one pot synthesis of azo dyes based on 1-naphthol under solvent-free conditions at room temperature. This method has some advantages, the reaction workup is very easy and the catalyst can be easily separated from the reaction mixture and one-pot procedure. The related products have been obtained in good to excellent yields, high purity and short reaction times. The structures of the products have been characterized by several techniques using UV-Vis, FT-IR, 1H NMR, 13C NMR and mass spectra.DOI: http://dx.doi.org/10.4314/bcse.v27i3.13

  4. Spectrophotometric determination of sildenafil citrate in pure form and in pharmaceutical formulation using some chromotropic acid azo dyes

    Science.gov (United States)

    Issa, Y. M.; El-Hawary, W. F.; Youssef, A. F. A.; Senosy, A. R.

    2010-04-01

    Two simple and highly sensitive spectrophotometric methods were developed for the quantitative determination of the drug sildenafil citrate (SC), Viagra, in pure form and in pharmaceutical formulations, through ion-associate formation reactions (method A) with mono-chromotropic acid azo dyes, chromotrope 2B (I) and chromotrope 2R (II) and ion-pair reactions (method B) with bi-chromotropic acid azo dyes, 3-phenylazo-6-o-carboxyphenylazo-chromotropic acid (III), bis-3,6-(o-hydroxyphenylazo)-chromotropic acid (IV), bis-3,6-(p-N,N-dimethylphenylazo)-chromotropic acid (V) and 3-phenylazo-6-o-hydroxyphenylazo-chromotorpic acid (VI). The reaction products, extractable in methylene chloride, were quantitatively measured at 540, 520, 540, 570, 600 and 575 nm using reagents, I-VI, respectively. The reaction conditions were studied and optimized. Beer's plots were linear in the concentration ranges 3.3-87.0, 3.3-96.0, 5.0-115.0, 2.5-125.0, 8.3-166.7 and 0.8-15.0 μg mL -1 with corresponding molar absorptivities 1.02 × 10 4, 8.34 × 10 3, 6.86 × 10 3, 5.42 × 10 3, 3.35 × 10 3 and 2.32 × 10 4 L mol -1 cm -1 using reagents I-VI, respectively. The limits of detection and Sandell's sensitivities were calculated. The methods were successfully applied to the analysis of commercial tablets (Vigoran) and the recovery study reveals that there is no interference from the common excipients that are present in tablets. Statistical comparison of the results was performed with regard to accuracy and precision using Student's t- and F-tests at 95% confidence level. There is no significant difference between the reported and proposed methods with regard to accuracy and precision.

  5. Effect of food azo dye tartrazine on learning and memory functions in mice and rats, and the possible mechanisms involved.

    Science.gov (United States)

    Gao, Yonglin; Li, Chunmei; Shen, Jingyu; Yin, Huaxian; An, Xiulin; Jin, Haizhu

    2011-08-01

    Tartrazine is an artificial azo dye commonly used in human food and pharmaceutical products. The present study was conducted to evaluate the toxic effect of tartrazine on the learning and memory functions in mice and rats. Animals were administered different doses of tartrazine for a period of 30 d and were evaluated by open-field test, step-through test, and Morris water maze test, respectively. Furthermore, the biomarkers of the oxidative stress and pathohistology were also measured to explore the possible mechanisms involved. The results indicated that tartrazine extract significantly enhanced active behavioral response to the open field, increased the escape latency in Morris water maze test and decreased the retention latency in step-through tests. The decline in the activities of catalase, glutathione peroxidase (GSH-Px), and superoxide dismutase (SOD) as well as a rise in the level of malonaldehyde (MDA) were observed in the brain of tartrazine-treated rats, and these changes were associated with the brain from oxidative damage. The dose levels of tartrazine in the present study produced a few adverse effects in learning and memory functions in animals. The mechanisms might be attributed to promoting lipid peroxidation products and reactive oxygen species, inhibiting endogenous antioxidant defense enzymes and the brain tissue damage. Tartrazine is an artificial azo dye commonly used in human food and pharmaceutical products. Since the last assessment carried out by the Joint FAO/WHO Expert Committee on Food Additives in 1964, many new studies have been conducted. However, there is a little information about the effects on learning and memory performance. The present study was conducted to evaluate the toxic effect of tartrazine on the learning and memory functions in animals and its possible mechanism involved. Based on our results, we believe that more extensive assessment of food additives in current use is warranted. © 2011 Institute of Food

  6. The effects of halide ions on the radiation-induced decoloration of azo and anthraquinone dyes in N2O-saturated aqueous solutions

    International Nuclear Information System (INIS)

    Suzuki, Nobutake; Tokunaga, Okihiro; Washino, Masamitsu

    1978-01-01

    The radiation-induced decoloration of azo and anthraquinone dyes was studied in N 2 O-saturated aqueous solutions containing halide ions. In the N 2 O-saturated solutions, the decoloration yield, G(-Dye), increased markedly upon the addition of Br - and I - , which are efficient scavengers of the OH radical. In the nitrogen-saturated solutions, however, the G(-Dye) decreased upon the addition of Br - and I - . Such an increase in the G(-Dye) upon the addition of Br - and I - in the N 2 O-saturated solutions is mainly attributable to the attacks of the halide radical anions, Br 2 - and I 2 - , on the ring structure of the dyes. On the other hand, the G(-Dye) was not changed upon the addition of Cl - in the N 2 O-saturated solution. This may be attributable to the very slow rate of the formation of Cl 2 - in a neutral solution. (auth.)

  7. Review of Polymer, Dye-Sensitized, and Hybrid Solar Cells

    Directory of Open Access Journals (Sweden)

    S. N. F. Mohd-Nasir

    2014-01-01

    Full Text Available The combination of inorganic nanoparticles semiconductor, conjugated polymer, and dye-sensitized in a layer of solar cell is now recognized as potential application in developing flexible, large area, and low cost photovoltaic devices. Several conjugated low bandgap polymers, dyes, and underlayer materials based on the previous studies are quoted in this paper, which can provide guidelines in designing low cost photovoltaic solar cells. All of these materials are designed to help harvest more sunlight in a wider range of the solar spectrum besides enhancing the rate of charge transfer in a device structure. This review focuses on developing solid-state dye-synthesized, polymer, and hybrid solar cells.

  8. Synthesis, dyeing performance on polyester fiber and antimicrobial studies of some novel pyrazolotriazine and pyrazolyl pyrazolone azo dyes

    Directory of Open Access Journals (Sweden)

    Hala F. Rizk

    2017-05-01

    Full Text Available 5-Amino-4-heterylazo-3-phenyl-1H-pyrazoles (2a–d were diazotized and coupled with malononitrile to give pyrazoloazo malononitrile which by heating in glacial acetic acid gave novel pyrazolo[5,1-c][1,2,4]triazine dyes (3a–d. Also, some diazopyrazolyl pyrazolone dyes (4a–h were synthesized by diazotization of 2a–d and coupled with some pyrazolone derivatives. The structure of the synthesized dyes was determined by elemental analysis and spectral data. All the synthesized compounds were applied as disperse dyes and their dyeing performance on polyester fabric was studied. The fastness and colorimetric properties were measured. The results revealed that the monoazo dyes have good fastness and good to moderate affinity to polyester fabric than diazo dyes. In addition, the synthesized dyes were screened for their antimicrobial activities against Staphylococcus aureus, Pseudomonas aeruginosa (Gram positive, Bacillus subtitles, Escherichia coli (Gram negative and Candida albicans, Aspergillus niger (Fungi. The results revealed that most of the prepared dyes have high antibacterial activity.

  9. Post-treatment of anaerobically degraded azo dye Acid Red 18 using aerobic moving bed biofilm process: Enhanced removal of aromatic amines

    International Nuclear Information System (INIS)

    Hosseini Koupaie, E.; Alavi Moghaddam, M.R.; Hashemi, S.H.

    2011-01-01

    Highlights: → Biofilm process was applied as post-treatment of anaerobically degraded an azo dye. → More than 65% of the dye total metabolites was completely mineralized. → Based on HPLC analysis, more than 80% of 1-naphthylamine-4-sulfonate was removed. → Inhibition of biofilm growth was increased with increasing the initial dye concentration. → Considerable porous morphology was observed in the SEM photographs of the biofilm. - Abstract: The application of aerobic moving bed biofilm process as post-treatment of anaerobically degraded azo dye Acid Red 18 was investigated in this study. The main objective of this work was to enhance removal of anaerobically formed the dye aromatic metabolites. Three separate sequential treatment systems were operated with different initial dye concentrations of 100, 500 and 1000 mg/L. Each treatment system consisted of an anaerobic sequencing batch reactor (An-SBR) followed by an aerobic moving bed sequencing batch biofilm reactor (MB-SBBR). Up to 98% of the dye decolorization and more than 80% of the COD removal occurred anaerobically. The obtained results suggested no significant difference in COD removal as well as the dye decolorization efficiency using three An-SBRs receiving different initial dye concentrations. Monitoring the dye metabolites through HPLC suggested that more than 80% of anaerobically formed 1-naphthylamine-4-sulfonate was completely removed in the aerobic biofilm reactors. Based on COD analysis results, at least 65-72% of the dye total metabolites were mineralized during the applied treatment systems. According to the measured biofilm mass and also based on respiration-inhibition test results, increasing the initial dye concentration inhibited the growth and final mass of the attached-growth biofilm in MB-SBBRs.

  10. Dye linked conjugated homopolymers: using conjugated polymer electroluminescence to optically pump porphyrin-dye emission

    DEFF Research Database (Denmark)

    Nielsen, K.T.; Spanggaard, H.; Krebs, Frederik C

    2004-01-01

    . Electroluminescent devices of the homopolymer itself and of the zinc-porphyrin containing polymer were prepared and the nature of the electroluminescence was characterized. The homopolymer segments were found to optically pump the emission of the zinc-porphyrin dye moities. The homopolymer exhibits blue......Zinc-porphyrin dye molecules were incorporated into the backbone of a conjugated polymer material by a method, which allowed for the incorporation of only one zinc-porphyrin dye molecule into the backbone of each conjugated polymer molecule. The electronic properties of the homopolymer were...

  11. Low-Cost Biodegradation and Detoxification of Textile Azo Dye C.I. Reactive Blue 172 by Providencia rettgeri Strain HSL1

    Directory of Open Access Journals (Sweden)

    Harshad Lade

    2015-01-01

    Full Text Available Present study focuses on exploitation of agricultural waste wheat bran (WB as growth medium for degradation of textile azo dye C.I. Reactive Blue 172 (RB 172 using a single bacterium P. rettgeri strain HSL1 (GenBank accession number JX853768.1. The bacterium was found to completely decolorize 50 mg L−1 of dye RB 172 within 20 h at 30 ± 0.2°C under microaerophilic incubation conditions. Additionally, significant reduction in COD (85% and TOC (52% contents of dye decolorized medium was observed which suggested its mineralization. Induction in the activities of azoreductase (159% and NADH-DCIP reductase (88% provided an evidence for reductive cleavage of dye RB 172. The HPLC, FTIR, and GC-MS analysis of decolorized products confirmed the degradation of dye into various metabolites. The proposed metabolic pathway for biodegradation of RB 172 has been elucidated which showed the formation of 2 intermediate metabolites, namely, 4-(ethenylsulfonyl aniline and 1-amino-1-(4-aminophenyl propan-2-one. The acute and phytotoxicity evaluation of degraded metabolites suggests that bacterial strain favors the detoxification of dye RB 172. Thus, WB could be utilized as a low-cost growth medium for the enrichment of bacteria and their further use for biodegradation of azo dyes and its derivatives containing wastes into nontoxic form.

  12. Bioelectricity Generation and Bioremediation of an Azo-Dye in a Microbial Fuel Cell Coupled Activated Sludge Process

    Science.gov (United States)

    Khan, Mohammad Danish; Abdulateif, Huda; Ismail, Iqbal M.; Sabir, Suhail; Khan, Mohammad Zain

    2015-01-01

    Simultaneous bioelectricity generation and dye degradation was achieved in the present study by using a combined anaerobic-aerobic process. The anaerobic system was a typical single chambered microbial fuel cell (SMFC) which utilizes acid navy blue r (ANB) dye along with glucose as growth substrate to generate electricity. Four different concentrations of ANB (50, 100, 200 and 400 ppm) were tested in the SMFC and the degradation products were further treated in an activated sludge post treatment process. The dye decolorization followed pseudo first order kinetics while the negative values of the thermodynamic parameter ∆G (change in Gibbs free energy) shows that the reaction proceeds with a net decrease in the free energy of the system. The coulombic efficiency (CE) and power density (PD) attained peak values at 10.36% and 2,236 mW/m2 respectively for 200 ppm of ANB. A further increase in ANB concentrations results in lowering of cell potential (and PD) values owing to microbial inhibition at higher concentrations of toxic substrates. Cyclic voltammetry studies revealed a perfect redox reaction was taking place in the SMFC. The pH, temperature and conductivity remain 7.5–8.0, 27(±2°C and 10.6–18.2 mS/cm throughout the operation. The biodegradation pathway was studied by the gas chromatography coupled with mass spectroscopy technique, suggested the preferential cleavage of the azo bond as the initial step resulting in to aromatic amines. Thus, a combined anaerobic-aerobic process using SMFC coupled with activated sludge process can be a viable option for effective degradation of complex dye substrates along with energy (bioelectricity) recovery. PMID:26496083

  13. Monopolar Electro-Coagulation Process for Azo Dye C.I. Acid Red 18 Removal from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Ghasem Azarian

    2014-12-01

    Full Text Available The discharge of wastewaters containing an untreated dye results in aesthetic problems and an increase in gases solubility, which causes light transmission inhibition into water bodies. In spite of advantages of physicochemical and biological methods, these processes produce huge amounts of sludge, toxic by-products and require several oxidant chemicals. By contrast, electrochemical processes because of their high versatility, high efficiency and eco-friendly properties are more acceptable. In the present study, the removal of azo dye Acid Red 18 and chemical oxygen demand (COD from synthetic wastewater by monopolar (EC process was investigated and key parameters such as operating time, current density (CD, initial pH and energy, and electrode consumption were optimized. It was found that the process had a very good efficiency in the removal of both COD and color; for the iron electrode, the maximum amounts of color and COD removal were 99.5% and 59.0%, respectively. An operating time of 45 min, pH of 7 and CD of 1.2 mA/cm2 was selected as the optimized condition. The optimization of variables is extremely crucial as it results in a decrease in costs, energy and electrode consumption. Overall, the iron electrode used less energy than the aluminum electrode and was more acceptable for use in this process due to economical reasons. The findings of UV/vis spectra illustrated that the structures of this dye were removed by the process. In comparison with traditional methods such as aerobic and anaerobic systems, the EC process is a suitable alternative for the treatment of wastewaters containing dye pollutants.

  14. Azo dye removal in a membrane-free up-flow biocatalyzed electrolysis reactor coupled with an aerobic bio-contact oxidation reactor

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Dan; Guo, Yu-Qi; Cheng, Hao-Yi; Liang, Bin; Kong, Fan-Ying [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, No. 202 Haihe Road, Harbin 150090 (China); Lee, Hyung-Sool [Department of Civil and Environmental Engineering, University of Waterloo, 200 University Avenue West Waterloo, Ontario, Canada N2L 3G1 (Canada); Wang, Ai-Jie, E-mail: waj0578@hit.edu.cn [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, No. 202 Haihe Road, Harbin 150090 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer A membrane-free up-flow biocatalyzed electrolysis reactor coupled with an aerobic bio-contact oxidation reactor was developed. Black-Right-Pointing-Pointer Alizarin Yellow R as the mode of azo dyes was efficiently converted to p-phenylenediamine (PPD) and 5-aminosalicylic acid (5-ASA). Black-Right-Pointing-Pointer PPD and 5-ASA were further oxidized in a bio-contact oxidation reactor. Black-Right-Pointing-Pointer The mechanism of UBER for azo dye removal was discussed. - Abstract: Azo dyes that consist of a large quantity of dye wastewater are toxic and persistent to biodegradation, while they should be removed before being discharged to water body. In this study, Alizarin Yellow R (AYR) as a model azo dye was decolorized in a combined bio-system of membrane-free, continuous up-flow bio-catalyzed electrolysis reactor (UBER) and subsequent aerobic bio-contact oxidation reactor (ABOR). With the supply of external power source 0.5 V in the UBER, AYR decolorization efficiency increased up to 94.8 {+-} 1.5%. Products formation efficiencies of p-phenylenediamine (PPD) and 5-aminosalicylic acid (5-ASA) were above 90% and 60%, respectively. Electron recovery efficiency based on AYR removal in cathode zone was nearly 100% at HRTs longer than 6 h. Relatively high concentration of AYR accumulated at higher AYR loading rates (>780 g m{sup -3} d{sup -1}) likely inhibited acetate oxidation of anode-respiring bacteria on the anode, which decreased current density in the UBER; optimal AYR loading rate for the UBER was 680 g m{sup -3} d{sup -1} (HRT 2.5 h). The subsequent ABOR further improved effluent quality. Overall the Chroma decreased from 320 times to 80 times in the combined bio-system to meet the textile wastewater discharge standard II in China.

  15. Azo dye removal in a membrane-free up-flow biocatalyzed electrolysis reactor coupled with an aerobic bio-contact oxidation reactor

    International Nuclear Information System (INIS)

    Cui, Dan; Guo, Yu-Qi; Cheng, Hao-Yi; Liang, Bin; Kong, Fan-Ying; Lee, Hyung-Sool; Wang, Ai-Jie

    2012-01-01

    Highlights: ► A membrane-free up-flow biocatalyzed electrolysis reactor coupled with an aerobic bio-contact oxidation reactor was developed. ► Alizarin Yellow R as the mode of azo dyes was efficiently converted to p-phenylenediamine (PPD) and 5-aminosalicylic acid (5-ASA). ► PPD and 5-ASA were further oxidized in a bio-contact oxidation reactor. ► The mechanism of UBER for azo dye removal was discussed. - Abstract: Azo dyes that consist of a large quantity of dye wastewater are toxic and persistent to biodegradation, while they should be removed before being discharged to water body. In this study, Alizarin Yellow R (AYR) as a model azo dye was decolorized in a combined bio-system of membrane-free, continuous up-flow bio-catalyzed electrolysis reactor (UBER) and subsequent aerobic bio-contact oxidation reactor (ABOR). With the supply of external power source 0.5 V in the UBER, AYR decolorization efficiency increased up to 94.8 ± 1.5%. Products formation efficiencies of p-phenylenediamine (PPD) and 5-aminosalicylic acid (5-ASA) were above 90% and 60%, respectively. Electron recovery efficiency based on AYR removal in cathode zone was nearly 100% at HRTs longer than 6 h. Relatively high concentration of AYR accumulated at higher AYR loading rates (>780 g m −3 d −1 ) likely inhibited acetate oxidation of anode-respiring bacteria on the anode, which decreased current density in the UBER; optimal AYR loading rate for the UBER was 680 g m −3 d −1 (HRT 2.5 h). The subsequent ABOR further improved effluent quality. Overall the Chroma decreased from 320 times to 80 times in the combined bio-system to meet the textile wastewater discharge standard II in China.

  16. Enhancement of polymer dye lasers by multifunctional photonic crystal lattice

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Xiao, Sanshui; Mortensen, Asger

    2009-01-01

    The light output of dye doped hybrid polymer band-edge lasers is increased more than 100 times by using a rectangular lattice photonic crystal, which provides both feedback and couples more pump light into the laser.......The light output of dye doped hybrid polymer band-edge lasers is increased more than 100 times by using a rectangular lattice photonic crystal, which provides both feedback and couples more pump light into the laser....

  17. Low-temperature-fabricated ZnO, AZO, and SnO{sub 2} nanoparticle-based dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Hong Hee; Park, Cheolmin; Choi, Wonkook; Cho, Sungjae; Moon, Byungjoon; Son, Dongick [Korea Institute of Science and Technology, Seoul (Korea, Republic of); Yonsei University, Seoul (Korea, Republic of)

    2014-11-15

    The authors investigated the microstructural and the electrical properties of ZnO, AZO, and SnO{sub 2} based dye-sensitized solar cells (DSSCs) fabricated using a low-temperature-processed (200 .deg. C) dyesensitized ZnO, AZO, and SnO{sub 2} nanoparticle thin film and a Pt catalyst deposited on ITO/glass by RF magnetron sputtering. A hydropolymer containing PEG (poly ethylene glycol) and PEO (poly ethylene oxide) is used to make uniformly-distributed ZnO, AZO, and SnO{sub 2} nanoparticle layer which forms a nano porous ZnO, AZO, and SnO{sub 2} network after heat treatment. The layer is then dye sensitized and sandwiched between two electrodes in an electrolyte to make a DSSC device. The highest measured parameters, the short-circuit current density (J{sub sc}), the open circuit potential (V{sub oc}), the fill factor (FF), and power conversion efficiency (η), of the DSSC fabricated wander optimized conditions were observed to be 5.10 mA/cm{sup 2}, 0.61 V, 0.46, and 1.43%, respectively.

  18. Adsorption of heavy metal ions and azo dyes by crosslinked nanochelating resins based on poly(methylmethacrylate-co-maleic anhydride

    Directory of Open Access Journals (Sweden)

    M. Ghaemy

    2014-03-01

    Full Text Available Chelating resins are suitable materials for the removal of heavy metals in water treatments. A copolymer, Poly(MMA-co-MA, was synthesized by radical polymerization of maleic anhydride (MA and methyl methacrylate (MMA, characterized and transformed into multifunctional nanochelating resin beads (80–150 nm via hydrolysis, grafting and crosslink reactions. The resin beads were characterized by swelling studies, field emission scanning electron microscopy (FESEM and Fourier transform infrared spectroscopy (FTIR. The main purpose of this work was to determine the adsorption capacity of the prepared resins (swelling ratio ~55% towards metal ions such as Hg2+, Cd2+, Cu2+ from water at three different pH values (3, 6 and 9. Variations in pH and types of metal ions have not significantly affected the chelation capacity of these resins. The maximum chelation capacity of one of the prepared resin beads (Co-g-AP3 for Hg2+ was 63, 85.8 and 71.14 mg/g at pH 3, 6 and 9, respectively. Approximately 96% of the metal ions could be desorbed from the resin. Adsorption capacity of these resins towards three commercial synthetic azo dyes was also investigated. The maximum adsorption of dye AY42 was 91% for the resin Co-g-AP3 at room temperature. This insures the applicability of the synthesized resins for industrial applications.

  19. Adsorption of Azo-Dye Orange II from Aqueous Solutions Using a Metal-Organic Framework Material: Iron- Benzenetricarboxylate

    Science.gov (United States)

    Rojas García, Elizabeth; López Medina, Ricardo; May Lozano, Marcos; Hernández Pérez, Isaías; Valero, Maria J.; Maubert Franco, Ana M.

    2014-01-01

    A Metal-Organic Framework (MOF), iron-benzenetricarboxylate (Fe(BTC)), has been studied for the adsorptive removal of azo-dye Orange II from aqueous solutions, where the effect of various parameters was tested and isotherm and kinetic models were suggested. The adsorption capacities of Fe(BTC) were much higher than those of an activated carbon. The experimental data can be best described by the Langmuir isotherm model (R2 > 0.997) and revealed the ability of Fe(BTC) to adsorb 435 mg of Orange II per gram of adsorbent at the optimal conditions. The kinetics of Orange II adsorption followed a pseudo-second-order kinetic model, indicating the coexistence of physisorption and chemisorption, with intra-particle diffusion being the rate controlling step. The thermodynamic study revealed that the adsorption of Orange II was feasible, spontaneous and exothermic process (−25.53 kJ·mol−1). The high recovery of the dye showed that Fe(BTC) can be employed as an effective and reusable adsorbent for the removal of Orange II from aqueous solutions and showed the economic interest of this adsorbent material for environmental purposes. PMID:28788289

  20. Adsorption of Azo-Dye Orange II from Aqueous Solutions Using a Metal-Organic Framework Material: Iron- Benzenetricarboxylate

    Directory of Open Access Journals (Sweden)

    Elizabeth Rojas García

    2014-12-01

    Full Text Available A Metal-Organic Framework (MOF, iron-benzenetricarboxylate (Fe(BTC, has been studied for the adsorptive removal of azo-dye Orange II from aqueous solutions, where the effect of various parameters was tested and isotherm and kinetic models were suggested. The adsorption capacities of Fe(BTC were much higher than those of an activated carbon. The experimental data can be best described by the Langmuir isotherm model (R2 > 0.997 and revealed the ability of Fe(BTC to adsorb 435 mg of Orange II per gram of adsorbent at the optimal conditions. The kinetics of Orange II adsorption followed a pseudo-second-order kinetic model, indicating the coexistence of physisorption and chemisorption, with intra-particle diffusion being the rate controlling step. The thermodynamic study revealed that the adsorption of Orange II was feasible, spontaneous and exothermic process (−25.53 kJ·mol−1. The high recovery of the dye showed that Fe(BTC can be employed as an effective and reusable adsorbent for the removal of Orange II from aqueous solutions and showed the economic interest of this adsorbent material for environmental purposes.

  1. Synthesized TiO{sub 2}/ZSM-5 composites used for the photocatalytic degradation of azo dye: Intermediates, reaction pathway, mechanism and bio-toxicity

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Kefu; Hu, Xin-Yan [College of the Environment and Ecology, Xiamen University, Xiamen (China); Chen, Bor-Yann; Hsueh, Chung-Chuan [Department of Chemical and Materials Engineering, National I-Lan University, I-Lan, Taiwan (China); Zhang, Qian [Department of Environmental Engineering, National Taiwan University, Taipei, Taiwan (China); Wang, Jiajie; Lin, Yu-Jung [College of the Environment and Ecology, Xiamen University, Xiamen (China); Chang, Chang-Tang, E-mail: ctchang73222@gmail.com [Department of Environmental Engineering, National I-Lan University, I-Lan, Taiwan (China)

    2016-10-15

    Highlights: • The major photo-catalytic degradation pathway of azo-dye was elaborated according to the identification of by-products from GC–MS and IC analysis. • Comparative assessment on characteristics of abiotic and biotic dye decolorization was analyzed. • EDTA (hole scavengers) and t-BuOH (radical scavengers) were used to determine the main active oxidative species in the system. • The toxicity effects of degradation intermediates of Reactive Black 5 (RB5) on the cellular respiratory activity were assessed. - Abstract: In this study, a one-step solid dispersion method was used to synthesize titanium dioxide (TiO{sub 2})/Zeolite Socony Mobil-5 (ZSM-5) composites with substantially reduced time and energy consumption. A degradation efficiency of more than 95% was achieved within 10 min using 50% PTZ (synthesized TiO{sub 2}/ZSM-5 composites with TiO{sub 2} contents of 50 wt% loaded on ZSM-5) at pH 7 and 25 °C. The possible degradation pathway of azo-dye Reactive Black 5 (RB5) was investigated using gas chromatography–mass spectrometry and ion chromatography (IC). The bonds between the N atoms and naphthalene groups are likely attacked first and cleaved by hydroxyl radicals, ultimately resulting in the decolorization and mineralization of the azo dye. A comparative assessment of the characteristics of abiotic and biotic dye decolorization was completed. In addition, the toxicity effects of the degradation intermediates of azo-dye RB5 on cellular respiratory activity were analyzed. The bio-toxicity results showed that the decay rate constants of CO{sub 2} production from the azo-dye RB5 samples at different degradation times increased initially and subsequently decreased, indicating that intermediates of higher toxicity could adhere to the catalyst surface and gradually destroyed by further photocatalytic oxidation. Additionally, EDTA (hole scavengers) and t-BuOH (radical scavengers) were used to detect the main active oxidative species in the system

  2. Kinetics and mechanism of azo dye destruction in advanced oxidation processes

    International Nuclear Information System (INIS)

    Wojnarovits, L.; Palfi, T.; Takacs, E.

    2007-01-01

    The kinetics and mechanism of dye destruction in advanced oxidation processes is discussed on the example of Apollofix Red (Ar-28) radiolysis in aqueous solution. When the reactive intermediate reacts with the color bearing part of the molecule causing with nearly 100% efficiency destruction of the conjugation, the dose dependence, or time dependence of color disappearance is linear. In this case, spectrophotometry can be used to follow-up dye decomposition. Linear dependence was observed when hydrated electrons or hydrogen atoms reacted with the dye. In hydroxyl radical reactions some colored products form with spectra similar to those of the starting dye molecules. For that reason, spectrophotometry gives false result about the intact dye molecule concentration. Analysis by the HPLC reveals logarithmic time dependence in agreement with a theoretical model developed

  3. Acid azo dye remediation in anoxic-aerobic-anoxic microenvironment under periodic discontinuous batch operation: bio-electro kinetics and microbial inventory.

    Science.gov (United States)

    Venkata Mohan, S; Suresh Babu, P; Naresh, K; Velvizhi, G; Madamwar, Datta

    2012-09-01

    Functional behavior of anoxic-aerobic-anoxic microenvironment on azo dye (C.I. Acid black 10B) degradation was evaluated in a periodic discontinuous batch mode operation for 26 cycles. Dye removal efficiency and azo-reductase activity (30.50 ± 1 U) increased with each feeding event until 13th cycle and further stabilized. Dehydrogenase activity also increased gradually and stabilized (2.0 ± 0.2 μg/ml) indicating the stable proton shuttling between metabolic intermediates providing higher number of reducing equivalents towards dye degradation. Voltammetric profiles showed drop in redox catalytic currents during stabilized phase also supports the consumption of reducing equivalents towards dye removal. Change in Tafel slopes, polarization resistance and other bioprocess parameters correlated well with the observed dye removal and biocatalyst behavior. Microbial community analysis documented the involvement of specific organism pertaining to aerobic and facultative functions with heterotrophic and autotrophic metabolism. Integrating anoxic microenvironment with aerobic operation might have facilitated effective dye mineralization due to the possibility of combining redox functions. Copyright © 2012 Elsevier Ltd. All rights reserved.

  4. Bioremoval of the azo dye Congo Red by the microalga Chlorella vulgaris.

    Science.gov (United States)

    Hernández-Zamora, Miriam; Cristiani-Urbina, Eliseo; Martínez-Jerónimo, Fernando; Perales-Vela, Hugo Virgilio; Ponce-Noyola, Teresa; Montes-Horcasitas, María del Carmen; Cañizares-Villanueva, Rosa Olivia

    2015-07-01

    Discharge of dye-containing wastewater by the textile industry can adversely affect aquatic ecosystems and human health. Bioremoval is an alternative to industrial processes for detoxifying water contaminated with dyes. In this work, active and inactive biomass of the microalga Chlorella vulgaris was assayed for the ability to remove Congo Red (CR) dye from aqueous solutions. Through biosorption and biodegradation processes, Chlorella vulgaris was able to remove 83 and 58 % of dye at concentrations of 5 and 25 mg L(-1), respectively. The maximum adsorption capacity at equilibrium was 200 mg g(-1). The Langmuir model best described the experimental equilibrium data. The acute toxicity test (48 h) with two species of cladocerans indicated that the toxicity of the dye in the effluent was significantly decreased compared to the initial concentrations in the influent. Daphnia magna was the species less sensitive to dye (EC50 = 17.0 mg L(-1)), followed by Ceriodaphnia dubia (EC50 = 3.32 mg L(-1)). These results show that Chlorella vulgaris significantly reduced the dye concentration and toxicity. Therefore, this method may be a viable option for the treatment of this type of effluent.

  5. Photo-oxidative degradation of Chicago Sky Blue azo dye on transition metal oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Slote, J.; Luo, J.; Hepel, M. [State Univ. of New York at Potsdam, NY (United States). Dept. of Chemistry; Zhong, C.-J. [State Univ. of New York at Binghamton, NY (United States). Dept. of Chemistry

    2003-07-01

    Every day, an average of 128 tons of dye staffs are discharged into waste water, causing environmental harm. The authors discussed the photo-electrical method for separating the semiconductor catalyst particles from the solution and direct control of the interfacial potential as an efficient and convenient method for degrading organic dyes. Photocurrent-potential measurements were made using a standard photoelectrochemical setup. It involved a microcomputer-controlled potentiostat and a 500 watts (W) quartz halogen lamp as the illumination source. The measurement of the photocurrent represented the difference between the current under illumination and current in the dark. Three-electrode electrochemical cells were used for all experiments. The best results concerning the degradation of dyes were obtained with tungsten oxides (WO3) and molybdenum oxides (MoO3) electrodes. Confirmation that the dyes had been fully degraded was obtained by performing absorbance measurements and a high performance liquid chromatography (HPLC) analysis of the samples after degradation. The effect on the rate of decolorisation process of Chicago Sky Blue, a diazo dye, and other dyes, of pH, potential, concentration, and type of supporting electrolyte was examined. The supporting electrolyte was found to have a strong influence on the degradation of diazo dye. Illumination with visible light yielded lower degradation rates than that with ultraviolet-visible light. It appears that Chicago Sky Blue dye sensitizes the semiconductor to expand the absorption of light energy well into visible range, despite the photoelectrochemical degradation of the dye being mainly induced by the ultraviolet light. The authors proposed the mechanisms of the reactions occurring during the photodegradation process. 6 refs., 1 fig.

  6. Photocatalytic Oxidation of Azo Dyes and Oxalic Acid in Batch Reactors and CSTR: Introduction of Photon Absorption by Dyes to Kinetic Models

    Directory of Open Access Journals (Sweden)

    I. Grčić

    2018-04-01

    Full Text Available The possibilities of treating industrial effluents and water purification by advanced oxidation processes have been extensively studied; photocatalysis has emerged as a feasible alternative solution. In order to apply the photocatalytic treatment on a larger scale, relevant modeling approaches are necessary. The scope of this work was to investigate the applicability of recently published kinetic models in different reactor systems (batch and CSTR under UVA or UVC irradiation and in combination with two types of TiO2 catalyst, AEROXIDE® P25 and PC-500 for degradation of azo dyes (C.I. Reactive Violet 2, and C.I. Mordant Yellow 10, oxalic acid and their mixtures. The influences of reactor geometry and irradiation intensities on pollutant oxidation efficiency were examined. The effect of photon absorption by dyes in water matrix was thoroughly studied. Relevant kinetic models were introduced to the mass balance for particular reactor system. Resulting models were sufficient for description of pollutant degradation in batch reactors and CSTR. Experimental results showed 1.15 times higher mineralization extents achieved after 7 cycles in CSTR than in batch photoreactor of similar geometry within the equivalent time-span. The application of CSTR in-series could simplify the photocatalytic water treatment on a larger scale.

  7. Treatment of an azo dye effluent by peroxi-coagulation and its comparison to traditional electrochemical advanced processes.

    Science.gov (United States)

    do Vale-Júnior, Edilson; da Silva, Djalma R; Fajardo, Ana S; Martínez-Huitle, Carlos A

    2018-04-05

    Peroxi-coagulation (PC) is an interesting new process that has not been widely studied in the literature. This work presents the application of this technology to treat an azo dye synthetic effluent, studying the effect of different parameters including initial pH, current density (j), initial dye concentration and supporting electrolyte. The two former variables significantly affected the colour removal of the wastewater, followed by the initial dye concentration and the kind of electrolyte, in a lesser extent. The optimum operating conditions achieved were initial pH of 3.0, j = 33.3 mA cm -2 , 100 mg L -1 of methyl orange (MO) and Na 2 SO 4 as supporting electrolyte. The performance of PC was also compared to other electrochemical advanced processes, under similar experimental conditions. Results indicate that the kinetic decay of the MO increases in the following order: electrocoagulation (EC) oxidation (EO) with electrogenerated H 2 O 2 oxidant character of the homogenous OH radicals generated by EF and PC approaches. The EO process with production of H 2 O 2 (EO-H 2 O 2 ) is limited by mass transport and the EC, as a separation method, takes longer times to achieve similar removal results. Energy requirements about 0.06 kWh g COD -1 , 0.09 kWh g COD -1 , 0.7 kWh g COD -1 and 0.1 kWh g COD -1 were achieved for PC, EF, EO-H 2 O 2 and EC, respectively. Degradation intermediates were monitored and carboxylic acids were detected for PC and EF processes, being rapidly removed by the former technology. PC emerges as a promising and competitive alternative for wastewaters depollution, among other oxidative approaches. Copyright © 2018 Elsevier Ltd. All rights reserved.

  8. Structure and reactivity of thiazolium azo dyes: UV-visible, resonance Raman, NMR, and computational studies of the reaction mechanism in alkaline solution.

    Science.gov (United States)

    Abbott, Laurence C; Batchelor, Stephen N; Moore, John N

    2013-03-07

    UV-visible absorption, resonance Raman, and (1)H NMR spectroscopy, allied with density functional theory (DFT) calculations, have been used to study the structure, bonding, and alkaline hydrolysis mechanism of the cationic thiazloium azo dye, 2-[2-[4-(diethylamino)phenyl]diazenyl]-3-methyl-thiazolium (1a), along with a series of six related dyes with different 4-dialkylamino groups and/or other phenyl ring substituents (2a-c, 3a-c) and the related isothiazolium azo dye, 5-[2-[4-(dimethylamino)phenyl]diazenyl]-2-methyl-isothiazolium (4). These diazahemicyanine dyes are calculated to have a similar low-energy structure that is cis, trans at the (iso)thiazolium-azo group, and for which the calculated Raman spectra provide a good match with the experimental data; the calculations on these structures are used to assign and discuss the transitions giving rise to the experimental spectra, and to consider the bonding and its variation between the dyes. UV-visible, Raman, and NMR spectra recorded from minutes to several weeks after raising the pH of an aqueous solution of 1a to ca. 11.5 show that the dominant initial step in the reaction is loss of diethylamine to produce a quinonimine (ca. hours), with subsequent reactions occurring on longer time scales (ca. days to weeks); kinetic analyses give a rate constant of 2.6 × 10(-2) dm(3) mol(-1) s(-1) for reaction of 1a with OH(-). UV-visible spectra recorded on raising the pH of the other dyes in solution show similar changes that are attributed to the same general reaction mechanism, but with different rate constants for which the dependence on structure is discussed.

  9. UV-visible-DAD and 1H-NMR spectroscopy data fusion for studying the photodegradation process of azo-dyes using MCR-ALS.

    Science.gov (United States)

    Fernández, Cristina; Pilar Callao, M; Larrechi, M Soledad

    2013-12-15

    The photodegradation process of three azo-dyes - Acid Orange 61, Acid Red 97 and Acid Brown 425 - was monitored simultaneously by ultraviolet-visible spectroscopy with diode array detector (UV-vis-DAD) and (1)H-nuclear magnetic resonance ((1)H-NMR). Multivariate curve resolution-alternating least squares (MCR-ALS) was applied to obtain the concentration and spectral profile of the chemical compounds involved in the process. The analysis of the H-NMR data suggests there are more intermediate compounds than those obtained with the UV-vis-DAD data. The fusion of UV-vis-DAD and the (1)H-NMR signal before the multivariate analysis provides better results than when only one of the two detector signals was used. It was concluded that three degradation products were present in the medium when the three azo-dyes had practically degraded. This study is the first application of UV-vis-DAD and (1)H-NMR spectroscopy data fusion in this field and illustrates its potential as a quick method for evaluating the evolution of the azo-dye photodegradation process. © 2013 Elsevier B.V. All rights reserved.

  10. Photocatalytic Removal of Azo Dye and Anthraquinone DyeUsing TiO2 Immobilised on Ceramic Tiles

    Directory of Open Access Journals (Sweden)

    P. N. Palanisamy

    2011-01-01

    Full Text Available The photocatalytic activity of TiO2 immobilized on different supports; cement and ceramic tile, was studied to decolorize two commercial dyes. The catalyst was immobilised by two different techniques, namely, slurry method on ceramic tile and powder scattering on cement. The degradation of the dyes was carried out using UV and solar irradiation. The comparative efficiency of the catalyst immobilised on two different supports was determined. The photodegradation process was monitored by UV-Vis spectrophotometer. The catalyst immobilised on ceramic tile was found to be better than the catalyst immobilised on cement. Experimental results showed that both illumination and the catalyst were necessary for the degradation of the dyes and UV irradiation is more efficient compared to solar irradiation.

  11. Role of surfactant derived intermediates in the efficacy and mechanism for radiation chemical degradation of a hydrophobic azo dye, 1-phenylazo-2-naphthol

    Energy Technology Data Exchange (ETDEWEB)

    Das, Laboni [Radiation & Photochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Chatterjee, Suchandra [Food Technology Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Naik, Devidas B. [Radiation & Photochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Adhikari, Soumyakanti, E-mail: asoumya@barc.gov.in [Radiation & Photochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

    2015-11-15

    Highlights: • Demonstration of the role of surfactant in the degradation of the hydrophobic dye. • First direct observation of the formation of “hydrazyl radical-parent” adduct. • Similar products obtained in the reaction of e{sup −}{sub aq} and ·OH radical in TX-100 medium. • Significant reduction in cytotoxicity of irradiated dye in aqueous–organic medium. • New mechanistic pathway could be delineated. - Abstract: A combined methodology involving gamma and pulse radiolysis, product analysis and toxicity studies has been adopted to comprehend the degradation process of a model hydrophobic azo dye, 1-phenylazo-2-naphthol, emphasizing the role of the surfactant, which is an integral part of textile waste. Two new and important findings are underlined in this article. The first is the direct attestation of the hydrazyl radical-parent adduct, formed in the reaction of the dye with e{sup −}{sub aq} followed by protonation and subsequent addition to the unreacted dye molecule. This has been confirmed from concentration dependent studies. Secondly, we have clearly shown that in the reaction of hydroxyl radical with the dye in Triton X-100 media, the initially produced TX radicals cause reductive degradation of the dye. Identification and detailed analysis of HPLC and GCMS data reveals that similar products are formed in both the reactions of e{sup −}{sub aq} and ·OH radicals. Moreover, the cytotoxicity of 10{sup −4} mol dm{sup −3} dye was found to be reduced significantly after irradiation. Thus, the present study not only depicts new pathways for the degradation of hydrophobic azo dye, but also demonstrates the role of a surfactant in the entire process.

  12. Mechanism of radiation destruction of dyes in polymers

    International Nuclear Information System (INIS)

    Belichenko, A.S.; Dyumaev, K.M.; Maslyukov, A.P.; Matyushin, G.A.; Nechitailo, V.S.

    1991-01-01

    Considering the experimental results, it might be expected that the mechanism of radiation destruction of dyed polymers by UV-and γ-irradiation should also be associated with a chemical reaction between dye molecules and oxyradicals which appear either on destruction of polymer macromolecules or on oxidation of macroradicals by the oxygen dissolved in the matrix. Thus, the radiation stability of dyes should depend on the rate of formation of primary radicals in the polymer under the action of UV- and γ-irradiation. As has been demostrated, this rate can be influenced by 'resonant' low-molecular additives which perform oscillative cross-relaxation. (author) 8 refs.; 2 figs

  13. Antimicrobial polymer films for food packaging

    Science.gov (United States)

    Concilio, S.; Piotto, S.; Sessa, L.; Iannelli, P.; Porta, A.; Calabrese, E. C.; Galdi, M. R.; Incarnato, L.

    2012-07-01

    New antimicrobial polymeric systems were realized introducing new antimicrobial azo compounds in PP and LDPE matrices. The polymeric materials containing different percentage of azo compounds were mold-casted and the obtained film were tested in vitro against Gram+ and Gram- bacteria and fungi. These results hold promise for the fabrication of bacteria-resistant polymer films by means of simple melt processing with antimicrobial azo-dyes.

  14. TiO2/Ag modified penta-bismuth hepta-oxide nitrate and its adsorption performance for azo dye removal

    Institute of Scientific and Technical Information of China (English)

    Eshraq Ahmed Abdullah; Abdul Halim Abdullah; Zulkarnain Zainal; Mohd Zobir Hussein; Tan Kar Ban

    2012-01-01

    A modified hydrophilic penta-bismuth hepta-oxide nitrate (Bi5O7NO3) surface was synthesized via a precipitation method using TiO2 and Ag as modified agents.The synthesized product was characterized by different analytical techniques.The removal efficiency was evaluated using mono- and di-sulphonated azo dyes as model pollutants.Different kinetic,isotherm and diffusion models were chosen to describe the adsorption process.X-ray photoelectron spectroscopy (XPS) results revealed no noticeable differences in the chemical states of modified adsorbent when compared to pure Bi5O7NO3; however,the presence of hydrophilic centres such as TiO2 and Ag developed positively charged surface groups and improved its adsorption performance to a wide range of azo dyes.Dyes removal was found to be a function of adsorbent dosage,initial dye concentration,solution pH and temperature.The reduction of Langrnuir 1,2-mixed order kinetics to the second or first-order kinetics could be successfully used to describe the adsorption of dyes onto the modified adsorbent.Mass transfer can be described by intra-particle diffusion at a certain stage,but it was not the rate limiting step that controlled the adsorption process.Homogenous behavior of adsorbent surface can be explored by applying Langmuir isotherm to fit the adsorption data.

  15. Novel 2-phenyl-3-{4’-[N-(4”-aminophenylcarbamoyl]-phenyl}-quinazoline-4(3Hone-6-sulphonic acidbased mono azo reactive dyes

    Directory of Open Access Journals (Sweden)

    DIVYESH R. PATEL

    2011-02-01

    Full Text Available A series of new heterocyclic mono azo reactive dyes 7a–m were prepared by diazotization of 2-phenyl-3-{4’-[N-(4”-aminophenylcarbamoyl]-phenyl}-quinazoline-4(3H-one-6-sulphonic acid (3 and coupling with various cyanurated coupling components 6a–m and their dyeing performance on silk, wool and cotton fibres was assessed. These dyes were found to give a variety of colour shades with very good depth and levelness on the fibres. All the compounds were identified by conventional method (IR and 1H-NMR and elemental analyses. The percentage dye bath exhaustion on different fibres was reasonably good and acceptable. The dyed fibre showed moderate to very good fastness to light, washing and rubbing.

  16. Characterization of azo dyes on Pt and Pt/polyaniline/dispersed Pt electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Molina, J.; Fernandez, J.; Rio, A.I. del; Bonastre, J. [Departamento de Ingenieria Textil y Papelera, EPS de Alcoy, Universitat Politecnica de Valencia, Plaza Ferrandiz y Carbonell s/n, 03801 Alcoy (Spain); Cases, F., E-mail: fjcases@txp.upv.es [Departamento de Ingenieria Textil y Papelera, EPS de Alcoy, Universitat Politecnica de Valencia, Plaza Ferrandiz y Carbonell s/n, 03801 Alcoy (Spain)

    2012-06-15

    The electrochemical characterization of two organic dyes (amaranth and procion orange MX-2R) has been performed on Pt electrodes and Pt electrodes coated with polyaniline and dispersed Pt. Electrodes with different Pt loads have been synthesized and characterized obtaining that a load of 300 {mu}g cm{sup -2} was the optimum one. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) was employed to observe the distribution and morphology of the Pt nanoparticles. The electroactivity of the electrodes has also been characterized by means of scanning electrochemical microscopy (SECM). The chemical characterization of Pt dispersed Pani coated Pt electrodes (Pt-Pani-Pt) was performed by means of X-ray photoelectron spectroscopy (XPS). The electrochemical characterization of the dyes has been performed by means of cyclic voltammetry. Voltammograms have shown that the presence of the dyes diminishes characteristic Pt oxidation and reduction peaks. However, redox processes due to the dyes, appeared in the voltammograms. The different species responsible of these redox processes were generated in the vicinity of the electrode and were not adsorbed on the electrode surface since after stirring, the different redox processes disappeared. Characterization with different scan rates showed that redox processes of both dyes were controlled by diffusion.

  17. Dye sensitized photovoltaic cells: Attaching conjugated polymers to zwitterionic ruthenium dyes

    DEFF Research Database (Denmark)

    Krebs, Frederik C; Biancardo, M.

    2006-01-01

    The synthesis of a zwitterionic ruthenium dye that binds to anatase surfaces and has a built-in functionality that allows for the attachment of a conjugated polymer chain is presented. The system was found to adsorb on the surface of anatase anchored by the ruthenium dye. Two types of devices were...... prepared: standard photoelectrochemical (PEC) solar cells and polymer solar cells. The PEC solar cells employed a sandwich geometry between TiO2 nanoporous photoanodes and Pt counter electrodes using LiI/I-2 in CH3CN as an electrolyte. The polymer solar cells employed planar anatase electrodes...

  18. Intermolecular energy transfer in binary systems of dye polymers

    Science.gov (United States)

    Liu, Lin-I.; Barashkov, Nikolay N.; Palsule, Chintamani P.; Gangopadhyay, Shubhra; Borst, Walter L.

    2000-10-01

    We present results and physical interpretations for the energy transfer mechanisms in two-component dye polymer systems. The data consist of fluorescence emission spectra and decays. Two dyes were embedded in an epoxypolymer base, and only they participated in the energy transfer. Following pulsed laser excitation of the donor dye, energy transfer took place to the accept dye. The possible transfer paths considered here were nonradiative and radiative transfer. The latter involves two steps, emission and absorption of a photon, and therefore is relatively slow, while nonradiative transfer is a fast single step resulting from direct Coulomb interactions. A predominantly nonradiative transfer is desirable for applications, for instance in wavelength shifters in high energy particle detection. We studied the concentration effects of the dyes on the energy transfer and obtained the relative quantum efficiencies of various wavelength shifters from the fluorescence emission spectra. For low acceptor concentrations, radiative transfer was found to dominate, while nonradiative transfer became dominant at increasing dye concentrations. The fluorescence decays were analyzed with a sum-of-exponentials method and with Förster kinetics. The sum of exponential model yielded mean decay times of the dye polymers useful for a general classification. The decay times decreased as desired with increasing acceptor concentration. The samples, in which nonradiative energy transfer dominated, were analyzed with Förster kinetics. As a result, the natural decay times of the donor and acceptor dyes and the critical radii for nonradiative energy transfer were obtained from a global best fit.

  19. Azo dyes decomposition on new nitrogen-modified anatase TiO{sub 2} with high adsorptivity

    Energy Technology Data Exchange (ETDEWEB)

    Janus, M., E-mail: mjanus@ps.pl [Szczecin University of Technology, Department of Sanitary Engineering, al. Piastow 50, 70-310 Szczecin (Poland); Szczecin University of Technology, Institute of Chemical and Environment Engineering, Department of Water Technology and Environment Engineering, ul. Pulaskiego 10, 70-322 Szczecin (Poland); Choina, J.; Morawski, A.W. [Szczecin University of Technology, Institute of Chemical and Environment Engineering, Department of Water Technology and Environment Engineering, ul. Pulaskiego 10, 70-322 Szczecin (Poland)

    2009-07-15

    New vis active photocatalyst was obtained by the modification of commercial anatase TiO{sub 2} (Police, Poland) in pressure reactor in an ammonia water atmosphere at 100 {sup o}C for 4 h. The photocatalytic activity of new material was tested during three azo dyes decomposition: monoazo (Reactive Read), diazo (Reactive Black) and poliazodye (Direct Green). Obtained photocatalyst had new bands at 1430-1440 cm{sup -1} attributed to the bending vibrations of NH{sub 4}{sup +} and at 1535 cm{sup -1} associated with NH{sub 2} groups or NO{sub 2} and NO. UV-vis/DR spectra of photocatalyst had also insignificant decrease in visible region. Fluorescence technique was used for studying the amount of hydroxyl radicals produced on TiO{sub 2} surface during visible light irradiation. The hydroxyl radicals produced react with coumarin present in the solution to form 7-hydroxycoumarin which has fluorescent capacity. Photocatalytic activity of modified TiO{sub 2} was compared with commercial titanium dioxide P25 (Degussa, Germany). The photocatalytic activity of TiO{sub 2}/N was higher than that of unmodified material and P25 under visible light irradiation. The ability for dye adsorption (Reactive Red) on photocatalyst surface was also tested. Unmodified TiO{sub 2} and P25 has isotherm of adsorption by Freundlich model, and nitrogen-modified TiO{sub 2} by Langmuir model. The presence of nitrogen at the surface of TiO{sub 2} significantly increased adsorption capacity of TiO{sub 2} as well as OH{center_dot} radicals formation under visible radiation.

  20. Evaluation of three reagent dosing strategies in a photo-Fenton process for the decolorization of azo dye mixtures

    International Nuclear Information System (INIS)

    Prato-Garcia, D.; Buitrón, Germán

    2012-01-01

    Highlights: ► Dosing strategies for a photo-Fenton process were evaluated. ► The dosing strategy had no effect of on the decolorization. ► The type of strategy influenced SUVA index, toxicity reduction and biodegradability. ► A continuous reagents supply was found to be the most adequate strategy. ► Decolorization as well as a less toxic and biodegradable effluent was produced. - Abstract: Three reagent dosing strategies used in the solar photo-assisted decolorization of a mixture of sulfonated dyes consisting of acid blue 113, acid orange 7 and acid red 151 were evaluated. Results demonstrated that the dosing strategy influenced both reagent consumption and the biodegradability and toxicity of the effluent. In one strategy (E 1 ), the Fenton's reactants were dosed in a punctual mode, while in the other two strategies (E 2 an E 3 ), the reactants were dosed continuously. In the E 2 strategy the reactants were dosed by varying the duration of the injection time. In the E 3 strategy, the reactants were dosed during 60 min at a constant rate, but with different concentrations. All cases showed that feeding the reactor between 40% and 60% of the maximal dose was sufficient to decolorize more than 90% of the mixture of azo dyes. The E 1 strategy was less effective for aromatic content reduction. Conversely, the continuous addition of the reagents (E 2 and E 3 strategies) improved the aromatic content removal. E 3 strategy was substantially more appropriate than E 1 strategy due to improved the effluent quality in two key areas: toxicity and biodegradability.

  1. Use of active consortia of constructed ternary bacterial cultures via mixture design for azo-dye decolorization enhancement

    International Nuclear Information System (INIS)

    Chen, B.-Y.; Wang, M.-Y.; Lu, W.-B.; Chang, J.-S.

    2007-01-01

    This first-attempt study used constructed bacterial consortia containing Escherichia coli DH5α (a weak decolorizer) and its UV-irradiated mutants (E. coli UVT1 and UV68; strong decolorizers) via equilateral triangle diagram and mixture experimental design to assess color removal during species evolution. The results showed that although strain DH5α was not an effective decolorizer, its presence might still played a significant role in affecting optimal color removal capabilities of mixed consortia (e.g., E. coli DH5α, UVT1 and UV68) for two model azo dyes; namely, reactive red 22 (RR22) and reactive black 5 (RB5). Contour analysis of ternary systems also clearly showed that decolorization of RR22 and RB5 by DH5α-containing active mixed consortia was more effective than mono-cultures of the stronger decolorizer alone (e.g., UVT1). The optimal composition of the mixed consortium (UV68, UVT1, DH5α) achieving the highest specific decolorization rate was (13%:58%:29%) and (0%:74%:26%) for decolorization of RR22 and RB5, respectively, with initial total cell density fixed at OD 600 = 3.5 ± 0.28

  2. Decolorizing of azo dye Reactive red 24 aqueous solution using exfoliated graphite and H2O2 under ultrasound irradiation.

    Science.gov (United States)

    Li, Mei; Li, Ji-Tai; Sun, Han-Wen

    2008-07-01

    At its natural pH (6.95), the decolorization of Reactive red 24 in ultrasound, ultrasound/H2O2, exfoliated graphite, ultrasound/exfoliated graphite, exfoliated graphite/H2O2 and ultrasound/exfoliated graphite/H2O2 systems were compared. An enhancement was observed for the decolorization in ultrasound/exfoliated graphite/H2O2 system. The effect of solution pH, H2O2 and exfoliated graphite dosages, and temperature on the decolorization of Reactive red 24 was investigated. The sonochemical treatment in combination with exfoliated graphite/H2O2 showed a synergistic effect for the decolorization of Reactive red 24. The results indicated that under proper conditions, there was a possibility to remove Reactive red 24 very efficient from aqueous solution. The decolorization of other azo dyes (Reactive red 2, Methyl orange, Acid red 1, Acid red 73, Acid red 249, Acid orange 7, Acid blue 113, Acid brown 75, Acid green 20, Acid yellow 42, Acid mordant brown 33, Acid mordant yellow 10 and Direct green 1) was also investigated, at their natural pH.

  3. Preparation, characterization of a ceria loaded carbon nanotubes nanocomposites photocatalyst and degradation of azo dye Acid Orange 7

    Directory of Open Access Journals (Sweden)

    Wen Tao

    2016-06-01

    Full Text Available A ceria loaded carbon nanotubes (CeO2/CNTs nanocomposites photocatalyst was prepared by chemical precipitation, and the preparation conditions were optimized using an orthogonal experiment method. HR-TEM, XRD, UV-Vis/DRS, TGA and XPS were used to characterize the photocatalyst. Nitrogen adsorption-desorption was employed to determine the BET specific surface area. The results indicated that the photocatalyst has no obvious impurities. CeO2 was dispersed on the carbon nanotubes with a good loading effect and high loading efficiency without agglomeration. The catalyst exhibits a strong ability to absorb light in the ultraviolet region and some ability to absorb light in the visible light region. The CeO2/CNTs nanocomposites photocatalyst was used to degrade azo dye Acid Orange 7 (40 mg/L. The optical decolorization rate was 66.58% after xenon lamp irradiation for 4 h, which is better than that of commercial CeO2 (43.13%. The results suggested that CeO2 loading on CNTs not only enhanced the optical decolorization rate but also accelerated the separation of CeO2/CNTs and water.

  4. Effects of Electrical Stimulation on the Degradation of Azo Dye in Three-Dimensional Biofilm Electrode Reactors

    Directory of Open Access Journals (Sweden)

    Xian Cao

    2017-04-01

    Full Text Available Three-dimensional biofilm electrode reactors (3D-BERs were constructed to degrade the azo dye Reactive Brilliant Red (RBR X-3B. The 3D-BERs with different influent concentrations and external voltages were individually studied to investigate their influence on the removal of X-3B. Experimental results showed that 3D-BERs have good X-3B removal efficiency; even when the influent concentration was 800 mg/L, removal efficiency of 73.4% was still achieved. In addition, the X-3B removal efficiency stabilized shortly after the influent concentration increased. In 3D-BERs, the average X-3B removal efficiency increased from 52.8% to 85.4% when the external voltage rose from 0 to 2 V. We further identified the intermediate products via UV-Vis and gas chromatography-mass spectrometry (GC-MS analyses, and discussed the potential mechanism of degradation. After the conjugate structure of X-3B was destroyed, all of the substances generated mainly consisted of lower-molecular-weight organics.

  5. Remediation of azo dyes by using household used black tea as an ...

    African Journals Online (AJOL)

    In the present study used black tea and its impregnates were used as an adsorbents for the removal of textile dyes such as methylene blue and malachite green. The impregnation technique was adopted for the preparation of metal impregnates. The present study shows that used black tea and its impregnate exhibit ...

  6. Photocatalytic oxidation of a reactive azo dye and evaluation of the ...

    African Journals Online (AJOL)

    driniev

    2004-07-03

    Jul 3, 2004 ... biological oxygen demand (BOD) test. The results ... Toxicity testing of photo- catalytically ... The dye solution contained in a flask was placed on a magnetic ..... opacity of the suspension in the excess of TiO2 particles (Fig. 4).

  7. Diffusion driven optofluidic dye lasers encapsulated into polymer chips

    DEFF Research Database (Denmark)

    Wienhold, Tobias; Breithaupt, Felix; Vannahme, Christoph

    2012-01-01

    Lab-on-a-chip systems made of polymers are promising for the integration of active optical elements, enabling e.g. on-chip excitation of fluorescent markers or spectroscopy. In this work we present diffusion operation of tunable optofluidic dye lasers in a polymer foil. We demonstrate that these ......Lab-on-a-chip systems made of polymers are promising for the integration of active optical elements, enabling e.g. on-chip excitation of fluorescent markers or spectroscopy. In this work we present diffusion operation of tunable optofluidic dye lasers in a polymer foil. We demonstrate...... that these first order distributed feedback lasers can be operated for more than 90 min at a pulse repetition rate of 2 Hz without fluidic pumping. Ultra-high output pulse energies of more than 10 μJ and laser thresholds of 2 μJ are achieved for resonator lengths of 3 mm. By introducing comparatively large on......-chip dye solution reservoirs, the required exchange of dye molecules is accomplished solely by diffusion. Polymer chips the size of a microscope cover slip (18 × 18 mm2) were fabricated in batches on a wafer using a commercially available polymer (TOPAS® Cyclic Olefin Copolymer). Thermal imprinting...

  8. Spectroscopic, thermal, catalytic and biological studies of Cu(II) azo dye complexes

    Science.gov (United States)

    El-Sonbati, A. Z.; Diab, M. A.; El-Bindary, A. A.; Shoair, A. F.; Hussein, M. A.; El-Boz, R. A.

    2017-08-01

    New complexes of copper(II) with azo compounds of 5-amino-2-(aryl diazenyl)phenol (HLn) are prepared and investigated by elemental analyses, molar conductance, IR, 1H NMR, UV-Visible, mass, ESR spectra, magnetic susceptibility measurements and thermal analyses. The complexes have a square planar structure and general formula [Cu(Ln)(OAc)]H2O. Study the catalytic activities of Cu(II) complexes toward oxidation of benzyl alcohol derivatives to carbonyl compounds were tested using H2O2 as the oxidant. The intrinsic binding constants (Kb) of the ligands (HLn) and Cu(II) complexes (1-4) with CT-DNA are determined. The formed compounds have been tested for biological activity of antioxidants, antibacterial against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria and yeast Candida albicans. Antibiotic (Ampicillin) and antifungal against (Colitrimazole) and cytotoxic compounds HL1, HL2, HL3 and complex (1) showed moderate to good activity against S. aureus, E. coli and Candida albicans, and also to be moderate on antioxidants and toxic substances. Molecular docking is used to predict the binding between the ligands with the receptor of breast cancer (2a91).

  9. A comparative study of polymer-dye interaction

    Directory of Open Access Journals (Sweden)

    Nandini R.

    2009-08-01

    Full Text Available The interaction between an anionic dye Methyl Orange and two poly cations namely, Poly (N-vinyl-4-methylpyridiniumiodide, (PC1 & Poly (vinylbenzyltriphenylphosphoniumchloride, (PC2 has been investigated by spectrophotometric method. The polymers are observed to induce metachromasy in the dye as evidenced from the considerable blue shift in the absorption maximum of the dye. The interaction constant and thermodynamic parameters of interaction have been determined by absorbance measurements at the metachromatic band. The effect of additives such as ionic salts, alcohols, urea and polyelectrolytes on the reversal of metachromasy has been studied and used to determine the stability of the metachromatic complex and to understand the nature of binding.

  10. Biodegradation of Azo Dye RO16 in Different Reactors by Immobilized Irpex lacteus

    Czech Academy of Sciences Publication Activity Database

    Tavčar, M.; Svobodová, Kateřina; Kuplenk, J.; Novotný, Čeněk; Pavko, A.

    2006-01-01

    Roč. 53, - (2006), s. 338-343 ISSN 1318-0207 R&D Projects: GA MŠk(CZ) 1P05ME828; GA AV ČR(CZ) IAA6020411; GA ČR(CZ) GP526/06/P102 Institutional research plan: CEZ:AV0Z50200510 Keywords : irpex lacteus * dye decolorization * trickle bed reactor Subject RIV: EE - Microbiology, Virology Impact factor: 0.703, year: 2006

  11. Application of acidic treated pumice as an adsorbent for the removal of azo dye from aqueous solutions: kinetic, equilibrium and thermodynamic studies

    Directory of Open Access Journals (Sweden)

    Samarghandi Mohammad

    2012-11-01

    Full Text Available Abstract Colored effluents are one of the important environment pollution sources since they contain unused dye compounds which are toxic and less-biodegradable. In this work removal of Acid Red 14 and Acid Red 18 azo dyes was investigated by acidic treated pumice stone as an efficient adsorbent at various experimental conditions. Removal of dye increased with increase in contact time and initial dye concentration, while decreased for increment in solution temperature and pH. Results of the equilibrium study showed that the removal of AR14 and AR18 followed Freundlich (r2>0.99 and Langmuir (r2>0.99 isotherm models. Maximum sorption capacities were 3.1 and 29.7 mg/g for AR 14 and AR18, namely significantly higher than those reported in the literature, even for activated carbon. Fitting of experimental data onto kinetic models showed the relevance of the pseudo-second order (r2>0.99 and intra-particle diffusion (r2>0.98 models for AR14 and AR18, respectively. For both dyes, the values of external mass transfer coefficient decreased for increasing initial dye concentrations, showing increasing external mass transfer resistance at solid/liquid layer. Desorption experiments confirmed the relevance of pumice stone for dye removal, since the pH regeneration method showed 86% and 89% regeneration for AR14 and AR18, respectively.

  12. Photophysical behavior of layer-by-layer electrostatic self-assembled film of azo dye Chromotrope-2R and a polycation

    Energy Technology Data Exchange (ETDEWEB)

    Hansda, Chaitali [Department of Physics, Jadavpur University, Jadavpur, Kolkata 700032 (India); Department of Physics, The University of Burdwan, Golapbag, Burdwan 713104 (India); Dutta, Bipan [Department of Physics, Sammilani Mahavidyalaya, Baghajatin Station, E.M. Bypass, Kolkata 700075 (India); Chakraborty, Utsav; Singha, Tanmoy [Department of Physics, Jadavpur University, Jadavpur, Kolkata 700032 (India); Hussain, Syed Arshad; Bhattacharjee, Debajyoti [Department of Physics, Tripura University, Suryamaninagar 799022, Tripura West (India); Paul, Sharmistha [West Bengal State Council of Science and Technology, Vigyan Chetana Bhavan, Sector-I, Salt Lake, Kolkata 700064 (India); Paul, Pabitra Kumar, E-mail: pabitra_tu@yahoo.co.in [Department of Physics, Jadavpur University, Jadavpur, Kolkata 700032 (India)

    2016-10-15

    This communication reports the fabrication of layer-by-layer electrostatic self-assembled films of an azo dye Chromotrope-2R (CH2R) and a Polycation poly(allylamine hydrochloride) (PAH) onto solid substrate. UV–vis absorption and steady state fluorescence emission spectroscopy successfully confirm the incorporation of dye molecules onto the PAH coated quartz substrate. The adsorption behavior of CH2R onto PAH backbone in LbL films highly depends upon the variation of the microenvironment namely pH of the dye solution from which the film was fabricated. PAH layer onto quartz substrate was able to swell sufficiently in the dye solution at very high pH. The Density functional theory was also utilized here to explain the origin of various spectral transitions from the ground electronic states for both in neutral and anionic form of CH2R. In LbL films the more closure association of dye molecules causes their aggregations which are reflected in their absorption and steady state fluorescence emission spectra when compared to those of pure dye solution. Atomic force microscopic images of LbL films assembled from CH2R aqueous solution at different pH clearly reveal the change in the surface morphology of the films and different degree of association of dye molecules in LbL films deposited at various pH of CH2R.

  13. Application of Acidic Treated Pumice as an Adsorbent for the Removal of Azo Dye from Aqueous Solutions:kinetic, Equilibrium and Thermodynamic Studies

    Directory of Open Access Journals (Sweden)

    Saied Bashiri

    2012-11-01

    Full Text Available Colored effluents are one of the important environment pollution sources since they contain unused dye compounds which are toxic and less-biodegradable. In this work removal of Acid Red 14 and Acid Red 18 azo dyes was investigated by acidic treated pumice stone as anefficient adsorbent at various experimental conditions. Removal of dye increased with increase in contact time and initial dye concentration, while decreased for increment in solution temperature and pH. Results of the equilibrium study showed that the removal ofAR14 and AR18 followed Freundlich (r2>0.99 and Langmuir (r2>0.99 isotherm models.Maximum sorption capacities were 3.1 and 29.7 mg/g for AR 14 and AR18, namely significantly higher than those reported in the literature, even for activated carbon. Fitting of experimental data onto kinetic models showed the relevance of the pseudo-second order (r2>0.99 and intra-particle diffusion (r2>0.98 models for AR14 and AR18, respectively. For both dyes, the values of external mass transfer coefficient decreased for increasing initial dye concentrations, showing increasing external mass transfer resistance at solid/liquid layer.Desorption experiments confirmed the relevance of pumice stone for dye removal, since the pH regeneration method showed 86% and 89 % regeneration for AR14 and AR18,respectively.

  14. Photophysical behavior of layer-by-layer electrostatic self-assembled film of azo dye Chromotrope-2R and a polycation

    International Nuclear Information System (INIS)

    Hansda, Chaitali; Dutta, Bipan; Chakraborty, Utsav; Singha, Tanmoy; Hussain, Syed Arshad; Bhattacharjee, Debajyoti; Paul, Sharmistha; Paul, Pabitra Kumar

    2016-01-01

    This communication reports the fabrication of layer-by-layer electrostatic self-assembled films of an azo dye Chromotrope-2R (CH2R) and a Polycation poly(allylamine hydrochloride) (PAH) onto solid substrate. UV–vis absorption and steady state fluorescence emission spectroscopy successfully confirm the incorporation of dye molecules onto the PAH coated quartz substrate. The adsorption behavior of CH2R onto PAH backbone in LbL films highly depends upon the variation of the microenvironment namely pH of the dye solution from which the film was fabricated. PAH layer onto quartz substrate was able to swell sufficiently in the dye solution at very high pH. The Density functional theory was also utilized here to explain the origin of various spectral transitions from the ground electronic states for both in neutral and anionic form of CH2R. In LbL films the more closure association of dye molecules causes their aggregations which are reflected in their absorption and steady state fluorescence emission spectra when compared to those of pure dye solution. Atomic force microscopic images of LbL films assembled from CH2R aqueous solution at different pH clearly reveal the change in the surface morphology of the films and different degree of association of dye molecules in LbL films deposited at various pH of CH2R.

  15. Catalytic role of Au-TiO{sub 2} nanocomposite on enhanced degradation of an azo-dye by electrochemically active biofilms: a quantized charging effect

    Energy Technology Data Exchange (ETDEWEB)

    Kalathil, Shafeer; Lee, Jintae; Cho, Moo Hwan, E-mail: mhcho@ynu.ac.kr [Yeungnam University, School of Chemical Engineering (Korea, Republic of)

    2013-01-15

    A green and sustainable approach to azo dye degradation by an electrochemically active biofilm (EAB) with Au-TiO{sub 2} nanocomposite assistance (average size of Au {approx}8 nm) has been developed with high efficiency and mineralization of toxic intermediates. The EAB-Au-TiO{sub 2} system degraded the dye more rapidly than the EAB without the nanocomposite, which indicated the catalytic role of the Au-TiO{sub 2} nanocomposite on the dye degradation. Toxicity measurements showed that the dye wastewater treated by the EAB-Au-TiO{sub 2} system was almost non-toxic while the dye wastewater treated by the EAB without the nanocomposite showed a high toxicity compared to the parent dye. Quantized charging and Fermi level equilibration within the Au-TiO{sub 2} nanocomposite may be attributed to the excellent catalytic activity of the nanocomposite on the dye degradation. A mechanism of the catalytic activity is also proposed. Redox behavior and quantized charging of the nanocomposite were confirmed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV), respectively. The proposed protocol can be effectively utilized in wastewater treatment applications.

  16. EXTRACTION OF MONOAZO DYES BY HYDROPHILIC EXTRACTANTS FROM AQUEOUS SOLUTIONS

    Directory of Open Access Journals (Sweden)

    Y. I. Korenman

    2012-01-01

    Full Text Available The extraction of mono azo dyes E102, E122, E110, E124, E129 from aqueous solutions with hydrophilic solvents (alcohols, esters, ketones and polymers (poly-N-vinylamides, polyethylene glycol was studied. The main regularities of extraction are established. The distribution coefficients and degree of extraction of dyes was estimate. The influence of the nature of solvents and polymers on the extraction of dyes from aqueous solutions are established.

  17. Decolorization of azo dye and generation of electricity by microbial fuel cell with laccase-producing white-rot fungus on cathode

    International Nuclear Information System (INIS)

    Lai, Chi-Yung; Wu, Chih-Hung; Meng, Chui-Ting; Lin, Chi-Wen

    2017-01-01

    Highlights: • A laccase-producing fungus on cathode of MFC was used to enhance degradation of azo dye. • Laccase-producing fungal cathodes performed better than laccase-free control cathodes. • A maximum power density of 13.38 mW/m"2 and an >90% decolorization of acid orange 7 were obtained. • Growing a fungal culture with continuous laccase production improved MFC’s electricity generation. - Abstract: Wood-degrading white-rot fungi produce many extracellular enzymes, including the multi-copper oxidative enzyme laccase (EC 1.10.3.2). Laccase uses atmospheric oxygen as the electron acceptor to catalyze a one-electron oxidation reaction of phenolic compounds and therefore has the potential to simultaneously act as a cathode catalyst in a microbial fuel cell (MFC) and degrade azo dye pollutants. In this study, the laccase-producing white-rot fungus Ganoderma lucidum BCRC 36123 was planted on the cathode surface of a single-chamber MFC to degrade the azo dye acid orange 7 (AO7) synergistically with an anaerobic microbial community in the anode chamber. In a batch culture, the fungus used AO7 as the sole carbon source and produced laccase continuously, reaching a maximum activity of 20.3 ± 0.3 U/L on day 19 with a 77% decolorization of the dye (50 mg/L). During MFC operations, AO7 in the anolyte diffused across a layer of polyvinyl alcohol-hydrogel that separated the cathode membrane from the anode chamber, and served as a carbon source to support the growth of, and production of laccase by, the fungal mycelium that was planted on the cathode. In such MFCs, laccase-producing fungal cathodes outperformed laccase-free controls, yielding a maximum open-circuit voltage of 821 mV, a closed-circuit voltage of 394 mV with an external resistance of 1000 Ω, a maximum power density of 13.38 mW/m"2, a maximum current density of 33 mA/m"2, and a >90% decolorization of AO7. This study demonstrates the feasibility of growing a white-rot fungal culture with continuous

  18. Comparison of three combined sequencing batch reactor followed by enhanced Fenton process for an azo dye degradation: Bio-decolorization kinetics study

    Energy Technology Data Exchange (ETDEWEB)

    Azizi, A., E-mail: armina_84@yahoo.com [Civil and Environmental Engineering Department, Amirkabir University of Technology, Hafez Ave., Tehran15875-4413 (Iran, Islamic Republic of); Alavi Moghaddam, M.R., E-mail: alavim@yahoo.com [Civil and Environmental Engineering Department, Amirkabir University of Technology, Hafez Ave., Tehran15875-4413 (Iran, Islamic Republic of); Maknoon, R., E-mail: rmaknoon@yahoo.com [Civil and Environmental Engineering Department, Amirkabir University of Technology, Hafez Ave., Tehran15875-4413 (Iran, Islamic Republic of); Kowsari, E., E-mail: kowsarie@aut.ac.ir [Department of Chemistry, Amirkabir University of Technology, Hafez Ave., Tehran 15875-4413 (Iran, Islamic Republic of)

    2015-12-15

    Highlights: • Three combined advanced SBR and enhanced Fenton process as post treatment was compared. • Higher biomass concentration, dye, COD and metabolites removal was presented together. • Pseudo zero and pseudo first-order bio-decolorization kinetics were observed in all SBRs. • High reduction of AR18 to intermediate metabolites was monitored by HPLC. - Abstract: The purpose of this research was to compare three combined sequencing batch reactor (SBR) – Fenton processes as post-treatment for the treatment of azo dye Acid Red 18 (AR18). Three combined treatment systems (CTS1, CTS2 and CTS3) were operated to investigate the biomass concentration, COD removal, AR18 dye decolorization and kinetics study. The MLSS concentration of CTS2 reached 7200 mg/L due to the use of external feeding in the SBR reactor of CTS2. The COD concentration remained 273 mg/L and 95 mg/L (initial COD = 3270 mg/L) at the end of alternating anaerobic–aerobic SBR with external feeding (An-A MSBR) and CTS2, respectively, resulting in almost 65% of Fenton process efficiency. The dye concentration of 500 mg/L was finally reduced to less than 10 mg/L in all systems indicating almost complete AR18 decolorization, which was also confirmed by UV–vis analysis. The dye was removed following two successive parts as parts 1 and 2 with pseudo zero-order and pseudo first-order kinetics, respectively, in all CTSs. Higher intermediate metabolites degradation was obtained using HPLC analysis in CTS2. Accordingly, a combined treatment system can be proposed as an appropriate and environmentally-friendly system for the treatment of the azo dye AR18 in wastewater.

  19. Interaction between toxic azo dye C.I. Acid Red 88 and serum albumins

    International Nuclear Information System (INIS)

    Naveenraj, Selvaraj; Solomon, Rajadurai Vijay; Venuvanalingam, Ponnambalam; Asiri, Abdullah M.; Anandan, Sambandam

    2013-01-01

    Serum albumin-toxic dye interaction studies will be of paramount importance in the field of toxicology due to its relation towards the distribution and transportation of dye in blood. In this regard, the binding between C.I. Acid Red 88 (AR88) and serum albumins (HSA and BSA) was investigated by using combination of spectroscopic and molecular modeling methods. The fluorescence results revealed that AR88 interact with serum albumins through the combination of static and dynamic quenching mechanism. The distance “r” between serum albumin and AR88 was obtained according to the Forster resonance energy transfer (FRET) theory. Synchronous fluorescence and CD spectral results showed alterations in the microenvironment and conformation of serum albumins. The molecular docking method is also employed to understand the interaction of AR88 with serum albumins. All these studies confirm that BSA has more affinity towards AR88 than that of HSA which suggests that AR88 is more easily transported in the body of bovid than human and so it is more hazardous to bovids. -- Highlights: • AR88 interacts with serum albumin through the combination of both static and dynamic quenching mechanism. • The binding site of AR88 in serum albumins is nearer to tryptophan moiety. • Circular Dichroism spectra showed that AR88 alters α-helicity of serum albumin. • This interaction study could be greatly imperative for further investigations in toxicology

  20. The comparison of spectra and dyeing properties of new azonaphthalimide with analogues azobenzene dyes on natural and synthetic polymers

    Directory of Open Access Journals (Sweden)

    Mozhgan Hosseinnezhad

    2017-05-01

    Full Text Available The aim of the present research was to prepare new acid dyes based on naphthalimides. In this respect a series of monoazo acid dyes have been obtained using 4-amino-N-methyl (alternatively N-butyl-1,8-naphthalimide, aniline and p-nitroaniline as diazo components. 2-Naphthol-6-sulfonic acid (Schaeffer’s acid and 1-naphthol-8-amino-3,6-disulfonic acid (H-acid were used as coupling components. The spectrophotometric properties of the synthesized dyes were investigated in various solvents and compared with analogues azobenzene dyes. It is found, when acid dyes are applied in various solvents and different pH, additional bathochromically shifted bands of different intensity appear in the electronic spectra. This effect is caused by the occurrence of the equilibrium of azo and hydrazone forms in the dyes. The synthesized acid dyes were applied on wool fabrics in order to consider their dyeing properties, fastnesses and the obtainable color gamut. The synthesized dyes represented that they have the ability of dyeing wool and polyamide fabrics and give red to violet hues with good wash, medium light, and good milling and perspiration fastnesses.

  1. Enhancing the electrochemical oxidation of acid-yellow 36 azo dye using boron-doped diamond electrodes by addition of ferrous ion

    International Nuclear Information System (INIS)

    Villanueva-Rodriguez, M.; Hernandez-Ramirez, A.; Peralta-Hernandez, J.M.; Bandala, Erick R.; Quiroz-Alfaro, Marco A.

    2009-01-01

    This work shows preliminary results on the electrochemical oxidation process (EOP) using boron-doped diamond (BDD) electrode for acidic yellow 36 oxidation, a common azo dye used in textile industry. The study is centred in the synergetic effect of ferrous ions and hydroxyl free radicals for improving discoloration of azo dye. The assays were carried out in a typical glass cell under potentiostatic conditions. On experimental conditions, the EOP was able to partially remove the dye from the reaction mixture. The reaction rate increased significantly by addition of Fe 2+ (1 mM as ferrous sulphate) to the system and by (assumed) generation of ferrate ion [Fe(VI)] over BDD electrode. Ferrate is considered as a highly oxidizing reagent capable of removing the colorant from the reaction mixture, in synergistic action with the hydroxyl radicals produced on the BDD surface. Further increases in the Fe 2+ concentration lead to depletion of the reaction rate probably due to the hydroxyl radical scavenging effect of Fe 2+ excess in the system.

  2. Azo dye removal in a membrane-free up-flow biocatalyzed electrolysis reactor coupled with an aerobic bio-contact oxidation reactor.

    Science.gov (United States)

    Cui, Dan; Guo, Yu-Qi; Cheng, Hao-Yi; Liang, Bin; Kong, Fan-Ying; Lee, Hyung-Sool; Wang, Ai-Jie

    2012-11-15

    Azo dyes that consist of a large quantity of dye wastewater are toxic and persistent to biodegradation, while they should be removed before being discharged to water body. In this study, Alizarin Yellow R (AYR) as a model azo dye was decolorized in a combined bio-system of membrane-free, continuous up-flow bio-catalyzed electrolysis reactor (UBER) and subsequent aerobic bio-contact oxidation reactor (ABOR). With the supply of external power source 0.5 V in the UBER, AYR decolorization efficiency increased up to 94.8±1.5%. Products formation efficiencies of p-phenylenediamine (PPD) and 5-aminosalicylic acid (5-ASA) were above 90% and 60%, respectively. Electron recovery efficiency based on AYR removal in cathode zone was nearly 100% at HRTs longer than 6 h. Relatively high concentration of AYR accumulated at higher AYR loading rates (>780 gm(-3) d(-1)) likely inhibited acetate oxidation of anode-respiring bacteria on the anode, which decreased current density in the UBER; optimal AYR loading rate for the UBER was 680 gm(-3) d(-1) (HRT 2.5 h). The subsequent ABOR further improved effluent quality. Overall the Chroma decreased from 320 times to 80 times in the combined bio-system to meet the textile wastewater discharge standard II in China. Copyright © 2012 Elsevier B.V. All rights reserved.

  3. Mechanism of azo dye degradation in Advanced Oxidation Processes: Degradation of Sulfanilic Acid Azochromotrop and its parent compounds in aqueous solution by ionizing radiation

    International Nuclear Information System (INIS)

    Palfi, Tamas; Wojnarovits, Laszlo; Takacs, Erzsebet

    2011-01-01

    Mechanistic studies were made on hydroxyl radical and hydrated electron reaction with Sulfanilic Acid Azochromotrop (SPADNS) as model azo dye in dilute aqueous solution. SPADNS contains 4,5-dihydroxynaphthalene-2,7-disulfonic acid part and 4-sulfophenylazo group. To establish the details of the reaction mechanism the reactions of two simpler molecules without 4-sulfophenylazo part were also studied: one of them contained one (in position 4, II), the other two (in positions 4 and 5, III) -OH groups. Hydroxyl radicals react with these molecules with radical addition to the naphthalene-2,7-disulfonic acid part. The adduct hydroxycyclohexadienyl type radical decays in radical-radical reactions, or undergoes a (pH dependent) water elimination to yield naphthoxy radical. The radical decay takes place on the ms timescale. Degradation efficiencies are 0.6-0.8. Hydrated electron in the case of the two simpler molecules reacts with the rings, while in the case of dye with the azo bond. Electron scavenging is followed by protonation, this reaction in the case of II and III yields cyclohexadienyl, while with the dye hydrazo radical. The efficiency of degradation with II and III is 0.2-0.6, while for SPADNS it is close to 1.

  4. Adsorption mechanism and kinetics of azo dye chemicals on oxide nanotubes: a case study using porous CeO_2 nanotubes

    International Nuclear Information System (INIS)

    Wu, Junshu; Wang, Jinshu; Du, Yucheng; Li, Hongyi; Jia, Xinjian

    2016-01-01

    Metal oxide nanotubes are believed to be promising materials with adsorption functionality for water purification due to their synergistic effect of the overall microscale morphology for easy separation and nanoscale surface characters providing enough surface active absorption sites. This work shows the synthesis of uniform hierarchical porous CeO_2 nanotubes via nanowire-directed templating method and describes the adsorption behavior of CeO_2 nanotubes for a typical azo dye Congo red which has resistance to oxidation and decoloration in natural conditions. Fourier transform infrared spectroscopy spectra provided the evidence that Congo red was successfully coated on the surface of CeO_2 nanotubes by both bidentate-type bridge link of Ce"4"+ cations from sulfonate SO_3"− groups and the electrostatic attraction between the protonated surface generated by oxygen vacancies and dissociated sulfonate groups. The adsorption kinetic data fitted well to the pseudo-second-order kinetic equation, whereas the Langmuir isotherm equation exhibited better correlation with the experimental data. The calculated maximum adsorption capacity from the isothermal model was 362.32 mg/g. In addition, the prepared CeO_2 nanotubes exhibited good recyclability and reusability as highly efficient adsorbents for Congo red removal after regeneration. These favorable performances enable the obtained CeO_2 nanotubes to be promising materials for dye removal from aqueous solution.Graphical AbstractCeO_2 nanotubes composed of crystallized nanoparticles exhibit well adsorption ability for a typical azo dye Congo red.

  5. Detection of Azo Dyes in Curry Powder Using a 1064-nm Dispersive Point-Scan Raman System

    Directory of Open Access Journals (Sweden)

    Sagar Dhakal

    2018-04-01

    Full Text Available Curry powder is extensively used in Southeast Asian dishes. It has been subject to adulteration by azo dyes. This study used a newly developed 1064 nm dispersive point-scan Raman system for detection of metanil yellow and Sudan-I contamination in curry powder. Curry powder was mixed with metanil yellow and (separately with Sudan-I, at concentration levels of 1%, 3%, 5%, 7%, and 10% (w/w. Each sample was packed into a nickel-plated sample container (25 mm × 25 mm × 1 mm. One Raman spectral image of each sample was acquired across the 25 mm × 25 mm surface area. Intensity threshold value was applied to the spectral images of Sudan-I mixtures (at 1593 cm−1 and metanil yellow mixtures (at 1147 cm−1 to obtain binary detection images. The results show that the number of detected adulterant pixels is linearly correlated with the sample concentration (R2 = 0.99. The Raman system was further used to obtain a Raman spectral image of a curry powder sample mixed together with Sudan-I and metanil yellow, with each contaminant at equal concentration of 5% (w/w. The multi-component spectra of the mixture sample were decomposed using self-modeling mixture analysis (SMA to extract pure component spectra, which were then identified as matching those of Sudan-I and metanil yellow using spectral information divergence (SID values. The results show that the 1064 nm dispersive Raman system is a potential tool for rapid and nondestructive detection of multiple chemical contaminants in the complex food matrix.

  6. Enhanced azo dye removal in a continuously operated up-flow anaerobic filter packed with henna plant biomass

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Jingang, E-mail: hjg@hdu.edu.cn [Institute of Environmental Science and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Wu, Mengke; Chen, Jianjun; Liu, Xiuyan; Chen, Tingting [Institute of Environmental Science and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Wen, Yue [State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Tang, Junhong; Xie, Zhengmiao [Institute of Environmental Science and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China)

    2015-12-15

    Highlights: • Henna stem mixed with ceramic media in UAF enhanced the removal of AO7. • Bio-reduction was the main AO7 removal pathway in henna-added UAF. • Adsorption and endogenous reduction were the main removal pathways in the control. • Henna played a multiple role in providing electron donors and redox mediator. - Abstract: Effects of henna plant biomass (stem) packed in an up-flow anaerobic bio-filter (UAF) on an azo dye (AO7) removal were investigated. AO7 removal, sulfanilic acid (SA) formation, and pseudo first-order kinetic constants for these reactions (k{sub AO7} and k{sub SA}) were higher in the henna-added UAF (R2) than in the control UAF without henna (R1). The maximum k{sub AO7} in R1 and R2 were 0.0345 and 0.2024 cm{sup −1}, respectively, on day 18; the corresponding molar ratios of SA formation to AO7 removal were 0.582 and 0.990. Adsorption and endogenous bio-reduction were the main AO7 removal pathways in R1, while in R2 bio-reduction was the dominant. Organics in henna could be released and fermented to volatile fatty acids, acting as effective electron donors for AO7 reduction, which was accelerated by soluble and/or fixed lawsone. Afterwards, the removal process weakened over time, indicating the demand of electron donation and lawsone-releasing during the long-term operation of UAF.

  7. Polymer photonic crystal dye lasers as optofluidic cell sensors

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Lopacinska, Joanna M.; Jakobsen, Mogens Havsteen

    2009-01-01

    Dye doped hybrid polymer lasers are implemented as label free evanescent field biosensors for detection of cells. It is demonstrated that although the coverage is irregular and the cells extend over several lattice constants, the emission wavelength depends linearly on the fraction of the surface...

  8. Iron promotion of the TiO2 photosensitization process towards the photocatalytic oxidation of azo dyes under solar-simulated light irradiation

    International Nuclear Information System (INIS)

    Castro, Camilo A.; Centeno, Aristobulo; Giraldo, Sonia A.

    2011-01-01

    Highlights: → Azo dye photooxidation occurs under strict combination of ultraviolet and visible irradiation of Fe-TiO 2 . → Fe 3+ enhances the TiO 2 photooxidation of azo dyes while decreases that of phenol. → UV irradiation leads to a decrease in photooxidation activity of Fe-TiO 2 photocatalysts. - Abstract: The photocatalytic oxidation of the azo dye Orange-II (Or-II) using Fe loaded TiO 2 (Fe-TiO 2 ) was studied under ultraviolet (UV), visible (vis) and simultaneous UV-vis irradiations using a solar light simulator. Photocatalysts were characterized by means of XRD, SEM-EDX, FTIR and DRS. Fe 3+ species, identified in XPS analyses, were responsible of the increased absorption of visible light. Moreover, DRS analyses showed a decrease in the bandgap due to Fe 3+ loading. Photocatalystic tests proved that Fe modification enhanced the TiO 2 photocatalytic activity towards Or-II photodegradation under simultaneous UV-vis irradiation. Even so, the performance of the Fe-TiO 2 samples towards the photodegradation of phenol, under UV irradiation, was lower than TiO 2 suggesting the recombination of the UV photogenerated electron-hole pair. Therefore, results evidence a Fe 3+ promotion of the electron caption in the photosensitization process of TiO 2 by Or-II acting as a sensitizer. Such process leads to the Or-II photooxidation under UV-vis irradiation by losing energy in electron transferring processes to sensitize TiO 2 , and, the formation of reactive oxygen species promoted by the injected electron to the TiO 2 conduction band.

  9. Bismuth Basic Nitrate as a Novel Adsorbent for Azo Dye Removal

    Directory of Open Access Journals (Sweden)

    E. A. Abdullah

    2012-01-01

    Full Text Available Bismuth basic nitrate (BBN and its TiO2-Ag modified sorbent, PTBA were successfully synthesized via a precipitation method. The structural characteristics of prepared sorbents were determined through different analytical techniques. The potential use of prepared sorbents for organic compounds' removal was evaluated using Methyl Orange and Sunset Yellow dyes as model pollutants in aqueous solutions. The experimental results showed that the presence of TiO2 and Ag particles during the crystal growth of bismuth basic nitrate has an effect on the crystal structure, point of zero charge (pHpzc, pore volume and diameter. The lower binding energy of Ti 2p core level peak indicates the octahedral coordination of TiO2 particles on the PTBA surface. The alteration of hydrophilic-hydrophobic characteristics of sorbent's surface improves the adsorptive performance of the modified sorbent and provides an efficient route for organic contaminants' removal from aqueous solutions.

  10. The effect of NCS- on the radiation-induced decoloration of azo and anthraquinone dyes in N2O-saturated aqueous solutions

    International Nuclear Information System (INIS)

    Suzuki, Nobutake; Hotta, Hiroshi

    1977-01-01

    The radiation-induced decoloration of azo and anthraquinone dyes was studied in N 2 O-saturated aqueous solutions containing NCS - . In the N 2 O-saturated solutions, the decoloration yield, G(-Dye), increased markedly upon the addition of NCS - , which is an efficient scavenger of the OH radical-that is, from 1.46 up to 2.10 for Acid Red 265 and from 0.51 up to 1.51 for Acid Blue 40 upon the addition of 1 mM NCS - . In the nitrogen-saturated solutions, however, the G(-Dye) decreased upon the addition of NCS - . It is concluded that the increase in the G(-Dye) upon the addition of NCS - in the N 2 O-saturated solutions is mainly attributable to the attack of the radical anion (NCS) 2 - on the ring structure of the dyes. This radical anion is formed through the following path: NCS - +OH → NCS+OH - and NCS+NCS - reversible (NCS) 2 - . At low NCS - concentrations, the G(-Dye) decreased for Acid Red 265 and increased for Acid Blue 40. This may be attributable to the larger reactivity of (NCS) 2 - on Acid Blue 40 than on Acid Red 265. (auth.)

  11. Decolorization of the azo dye Acid Orange 51 by laccase produced in solid culture of a newly isolated Trametes trogii strain.

    Science.gov (United States)

    Daâssi, Dalel; Zouari-Mechichi, Hela; Frikha, Fakher; Martinez, Maria Jesus; Nasri, Moncef; Mechichi, Tahar

    2013-04-01

    This study concerns the decolorization and detoxification of the azo dye Acid Orange 51 (AO51) by crude laccase from Trametes trogii produced in solid culture using sawdust as support media. A three-level Box-Behnken factorial design with four factors (enzyme concentration, 1-hydroxybenzotriazole (HBT) concentration, dye concentration and reaction time) combined with response surface methodology was applied to optimize AO51 decolorization. A mathematical model was developed showing the effect of each factor and their interactions on color removal. The model predicted that Acid Orange 51 decolorization above 87.87 ± 1.27 % could be obtained when enzyme concentration, HBT concentration, dye concentration and reaction time were set at 1 U/mL, 0.75 mM, 60 mg/L and 2 days, respectively. The experimental values were in good agreement with the predicted ones and the models were highly significant, the correlation coefficient (R 2 ) being 0.9. Then the desirability function was employed to determine the optimal decolorization condition for each dye and minimize the process cost simultaneously. In addition, germination index assay showed that laccase-treated dye was detoxified; however in the presence of HBT, the phytotoxicity of the treated dye was increased. By using cheap agro-industrial wastes, such as sawdust, a potential laccase was obtained. The low cost of laccase production may further broaden its application in textile wastewater treatment.

  12. Descoloração redutiva de corantes azo e o efeito de mediadores redox na presença do aceptor de elétrons sulfato Reductive decolourisation of azo dyes and the effect of redox mediators in the presence of the electron acceptor sulfate

    Directory of Open Access Journals (Sweden)

    Mayara Carantino Costa

    2010-01-01

    Full Text Available We investigated the impact of sulphate and the redox mediator Anthraquinone-2,6-disulfonate (AQDS on the decolorization of the azo dyes Congo Red (CR and Reactive Black 5 (RB5. In anaerobic reactors free of extra sulphate dosage, the color removal efficiency decreased drastically when the external electron donor ethanol was removed. In presence of an extra dosage of sulphate, CR decolourisations were 47.8% (free of AQDS and 96.5% (supplemented with AQDS. The decolourisations achieved in both reactors with RB5 were lower than the ones found with CR. Finally, the biogenic sulphide contribution on azo dye reduction was negligiable.

  13. Synthesis, spectroscopic and TD-DFT quantum mechanical study of azo-azomethine dyes. A laser induced trans-cis-trans photoisomerization cycle.

    Science.gov (United States)

    Georgiev, Anton; Kostadinov, Anton; Ivanov, Deyan; Dimov, Deyan; Stoyanov, Simeon; Nedelchev, Lian; Nazarova, Dimana; Yancheva, Denitsa

    2018-03-05

    This paper describes the synthesis, spectroscopic characterization and quantum mechanical calculations of three azo-azomethine dyes. The dyes were synthesized via condensation reaction between 4-(dimethylamino)benzaldehyde and three different 4-aminobenzene azo dyes. Quantum chemical calculations on the optimized molecular geometry and electron densities of the trans (E) and cis (Z) isomers and their vibrational frequencies have been computed by using DFT/B3LYP density-functional theory with 6-311++G(d,p) basis set in vacuo. The thermodynamic parameters such as total electronic energy E (RB3LYP), enthalpy H 298 (sum of electronic and thermal enthalpies), free Gibbs energy G 298 (sum of electronic and thermal free Gibbs energies) and dipole moment μ were computed for trans (E) and cis (Z) isomers in order to estimate the ΔE trans→cis , Δμ trans→cis, ΔH trans→cis , ΔG trans→cis and ΔS trans→cis values. After molecular geometry optimization the electronic spectra have been obtained by TD-DFT calculations at same basis set and correlated with the spectra of vapour deposited nanosized films of the dyes. The NBO analysis was performed in order to understand the intramolecular charge transfer and energy of resonance stabilization. Solvatochromism was investigated by UV-VIS spectroscopy in five different organic solvents with increasing polarity. The dynamic photoisomerization experiments have been performed in DMF by pump lasers λ=355nm (mostly E→Z) and λ=491nm (mostly Z→E) in spectral region 300nm - 800nm at equal concentrations and times of illumination in order to investigate the photodynamical trans-cis-trans properties of the CHN and NN chromophore groups of the dyes. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. ISOLATION AND CHARACTERIZATION OF A MOLYBDENUM-REDUCING AND AZO-DYE DECOLORIZING SERRATIA MARCESCENS STRAIN NENI-1 FROM INDONESIAN SOIL

    Directory of Open Access Journals (Sweden)

    Neni Gusmanizar

    2016-01-01

    Full Text Available Heavy metals and organic xenobiotics including dyes are important industrial components with their usage amounting to the millions of tonnes yearly. Their presence in the environment is a serious pollution issue globally. Bioremediation of these pollutants using microbes with multiple detoxification capacity is constantly being sought. In this work we screen the ability of a molybdenum-reducing bacterium isolated from contaminated soil to decolorize various azo and triphenyl methane dyes. The bacterium reduces molybdate to molybdenum blue (Mo-blue optimally at pH 6.0, and temperatures of between 25 and 40oC. Glucose was the best electron donor for supporting molybdate reduction followed by sucrose, trehalose, maltose, d-sorbitol, dmannitol, d-mannose, myo-inositol, glycerol and salicin in descending order. Other requirements include a phosphate concentration of between 5.0 and 7.5 mM and a molybdate concentration between 10 and 20 mM. The absorption spectrum of the Moblue produced was similar to previous Mo-reducing bacterium, and closely resembles a reduced phosphomolybdate. Molybdenum reduction was inhibited by copper, silver and mercury at 2 ppm by 43.8%, 42.3% and 41.7%, respectively. We screen for the ability of the bacterium to decolorize various dyes. The bacterium was able to decolorize the dye Congo Red. Biochemical analysis resulted in a tentative identification of the bacterium as Serratia marcescens strain Neni-1. The ability of this bacterium to detoxify molybdenum and decolorize azo dye makes this bacterium an important tool for bioremediation.

  15. Treatment of a non-azo dye aqueous solution by CWAO in continuous reactor using a Ni catalyst derived from hydrotalcite-like precursor

    Energy Technology Data Exchange (ETDEWEB)

    Vallet, Ana, E-mail: avallet@quim.ucm.es [Grupo de Catalisis y Procesos de Separacion (CyPS), Departamento de Ingenieria Quimica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Besson, Michele, E-mail: michele.besson@ircelyon.univ-lyon1.fr [IRCELYON, Institut de recherches sur la catalyse et l' environnement de Lyon, UMR5256 CNRS-Universite Lyon1, 2 Avenue Albert Einstein, F-69626 Villeurbanne Cedex (France); Ovejero, Gabriel; Garcia, Juan [Grupo de Catalisis y Procesos de Separacion (CyPS), Departamento de Ingenieria Quimica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer Ni supported over hydrotalcite calcined precursors as catalyst. Black-Right-Pointing-Pointer Catalytic wet air oxidation in trickle bed reactor for Basic Yellow 11 removal. Black-Right-Pointing-Pointer Dye removal depends on temperature, initial dye concentration and flow rate. Black-Right-Pointing-Pointer The catalyst proved to be stable and efficient for the dye degradation. - Abstract: Catalytic wet air oxidation (CWAO) of a Basic Yellow 11 (BY11) aqueous solution, chosen as a model of a hardly biodegradable non-azo dye was carried out in a continuous-flow trickle-bed reactor, using nickel supported over hydrotalcite precursor calcined at 550 Degree-Sign C. An increase in the reaction temperature (120-180 Degree-Sign C), and a decrease in dye concentration (1000-3000 ppm) or liquid flow rate (0.1-0.7 mL min{sup -1}) enhanced the CWAO performance in a 30 and 19% for the variation of the temperature and concentration respectively. After a small leaching observed within the first hours, the catalyst proved to be very stable during the 65-day reaction. The CWAO process was found to be very efficient, achieving BY11 conversion up to 95% and TOC conversion up to 85% at 0.1 mL min{sup -1} and 180 Degree-Sign C under 5 MPa air.

  16. A comparative study of quantum yield and electrical energy per order (E(Eo)) for advanced oxidative decolourisation of reactive azo dyes by UV light.

    Science.gov (United States)

    Muruganandham, M; Selvam, K; Swaminathan, M

    2007-06-01

    This paper evaluates the quantum yield and electrical energy per order (E(Eo)) efficiency of Reactive Orange 4 (RO4) and Reactive Yellow 14 (RY14) azo dyes by three advanced oxidation processes (AOPs). Both dyes were completely decolourised by all these processes. The relative decolourisation efficiencies of these processes were in the following order: Fe(2+)/H(2)O(2)/UV>UV/TiO(2)>UV/H(2)O(2). The low efficiency of UV/H(2)O(2) process is mainly due to low UV absorption by hydrogen peroxide at the 365nm. The figure of merit E(Eo) values showed that UV/H(2)O(2) process consumes more electrical energy than the other two processes. The electrical energy consumption is in the following order: UV/H(2)O(2)>UV/TiO(2)>Fe(2+)/H(2)O(2)/UV. At low initial dye concentration higher quantum yield was observed in UV/TiO(2) process, whereas in photo-Fenton process higher quantum yield was observed at high initial dye concentration. The structure of dye molecule also influences the quantum yield and E(Eo) value.

  17. A comparative investigation on adsorption performances of mesoporous activated carbon prepared from waste rubber tire and activated carbon for a hazardous azo dye-Acid Blue 113

    International Nuclear Information System (INIS)

    Gupta, V.K.; Gupta, Bina; Rastogi, Arshi; Agarwal, Shilpi; Nayak, Arunima

    2011-01-01

    Research highlights: → The system is cheap, efficient and fast for the removal of dyes from waters. → Higher adsorption capacity is due to higher mesoporous volume of the adsorbent. → The rate determining step of the adsorption process is particle diffusion. - Abstract: A mesoporous carbon developed from waste tire rubber, characterized by chemical analysis, FTIR, and SEM studies, was used as an adsorbent for the removal and recovery of a hazardous azo dye, Acid Blue 113. Surface area, porosity, and density were determined. The adsorption of the dye over the prepared adsorbent and a commercial activated carbon was achieved under different pH, adsorbate concentration, sieve size, adsorbent dosage, contact time and temperature conditions. Langmuir and Freundlich adsorption isotherm models were applied and thermodynamic parameters were calculated. Kinetic studies indicated that the adsorption process follow first order kinetics and particle diffusion mechanisms are operative. By percolating the dye solution through fixed-bed columns the bulk removal of the Acid Blue 113 was carried out and necessary parameters were determined to find out the percentage saturation of both the columns. Recovery of the dye was made by eluting 0.1 M NaOH through the column.

  18. Treatment of a non-azo dye aqueous solution by CWAO in continuous reactor using a Ni catalyst derived from hydrotalcite-like precursor

    International Nuclear Information System (INIS)

    Vallet, Ana; Besson, Michèle; Ovejero, Gabriel; García, Juan

    2012-01-01

    Highlights: ► Ni supported over hydrotalcite calcined precursors as catalyst. ► Catalytic wet air oxidation in trickle bed reactor for Basic Yellow 11 removal. ► Dye removal depends on temperature, initial dye concentration and flow rate. ► The catalyst proved to be stable and efficient for the dye degradation. - Abstract: Catalytic wet air oxidation (CWAO) of a Basic Yellow 11 (BY11) aqueous solution, chosen as a model of a hardly biodegradable non-azo dye was carried out in a continuous-flow trickle-bed reactor, using nickel supported over hydrotalcite precursor calcined at 550 °C. An increase in the reaction temperature (120–180 °C), and a decrease in dye concentration (1000–3000 ppm) or liquid flow rate (0.1–0.7 mL min −1 ) enhanced the CWAO performance in a 30 and 19% for the variation of the temperature and concentration respectively. After a small leaching observed within the first hours, the catalyst proved to be very stable during the 65-day reaction. The CWAO process was found to be very efficient, achieving BY11 conversion up to 95% and TOC conversion up to 85% at 0.1 mL min −1 and 180 °C under 5 MPa air.

  19. A comparative study of quantum yield and electrical energy per order (E Eo) for advanced oxidative decolourisation of reactive azo dyes by UV light

    International Nuclear Information System (INIS)

    Muruganandham, M.; Selvam, K.; Swaminathan, M.

    2007-01-01

    This paper evaluates the quantum yield and electrical energy per order (E Eo ) efficiency of Reactive Orange 4 (RO4) and Reactive Yellow 14 (RY14) azo dyes by three advanced oxidation processes (AOPs). Both dyes were completely decolourised by all these processes. The relative decolourisation efficiencies of these processes were in the following order: Fe 2+ /H 2 O 2 /UV > UV/TiO 2 > UV/H 2 O 2 . The low efficiency of UV/H 2 O 2 process is mainly due to low UV absorption by hydrogen peroxide at the 365 nm. The figure of merit E Eo values showed that UV/H 2 O 2 process consumes more electrical energy than the other two processes. The electrical energy consumption is in the following order: UV/H 2 O 2 > UV/TiO 2 > Fe 2+ /H 2 O 2 /UV. At low initial dye concentration higher quantum yield was observed in UV/TiO 2 process, whereas in photo-Fenton process higher quantum yield was observed at high initial dye concentration. The structure of dye molecule also influences the quantum yield and E Eo value

  20. Electrochemical characteriztion of the bioanode during simultaneous azo dye decolorization and bioelectricity generation in an air-cathode single chambered microbial fuel cell

    International Nuclear Information System (INIS)

    Sun Jian; Hu Yongyou; Hou Bin

    2011-01-01

    To achieve high power output based on simultaneously azo dye decolorization using microbial fuel cell (MFC), the bioanode responses during decolorization of a representative azo dye, Congo red, were investigated in an air-cathode single chambered MFC using representative electrochemical techniques. It has been found that the maximum stable voltage output was delayed due to slowly developed anode potential during Congo red decolorization, indicating that the electrons recovered from co-substrate are preferentially transferred to Congo red rather than the bioanode of the MFC and Congo red decolorization is prior to electricity generation. Addition of Congo red had a negligible effect on the Ohmic resistance (R ohm ) of the bioanode, but the charge-transfer resistance (R c ) and the diffusion resistance (R d ) were significantly influenced. The R c and R d firstly decreased then increased with increase of Congo red concentration, probably due to the fact that the Congo red and its decolorization products can act as electron shuttle for conveniently electrons transfer from bacteria to the anode at low concentration, but result in accelerated consumption of electrons at high concentration. Cyclic voltammetry results suggested that Congo red was a more favorable electron acceptor than the bioanode of the MFC. Congo red decolorization did not result in a noticeable decrease in peak catalytic current until Congo red concentration up to 900 mg l -1 . Long-term decolorization of Congo red resulted in change in catalytic active site of anode biofilm.

  1. The influence of Triton X-100 surfactant on the morphology and properties of zinc sulfide nanoparticles for applications in azo dyes degradation

    Energy Technology Data Exchange (ETDEWEB)

    Dumbrava, Anca, E-mail: adumbrava@univ-ovidius.ro [Department of Chemistry and Chemical Engineering, Ovidius University of Constanta, 124 Mamaia Blvd., Constanta 900527 (Romania); Berger, Daniela, E-mail: danaberger01@yahoo.com [University Politehnica of Bucharest, Department of Inorganic Chemistry, Physical Chemistry and Electrochemistry, Polizu Street 1-7, Bucharest 011061 (Romania); Prodan, Gabriel [Electron Microscopy Laboratory, Ovidius University of Constanta, 124 Mamaia Blvd., Constanta 900527 (Romania); Matei, Cristian [University Politehnica of Bucharest, Department of Inorganic Chemistry, Physical Chemistry and Electrochemistry, Polizu Street 1-7, Bucharest 011061 (Romania); Moscalu, Florin [Department of Physics, Ovidius University of Constanta, 124 Mamaia Blvd., Constanta 900527 (Romania); Diacon, Aurel [University Politehnica of Bucharest, Department of Bioresources and Polymer Science, Polizu Street 1-7, Bucharest 011061 (Romania)

    2017-06-01

    Herein we report the synthesis, by two different routes, of ZnS nanoparticles capped with Triton X-100 (TX), which were characterized by X-ray diffraction, transmission electron microscopy, high resolution electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy, FTIR spectroscopy, UV–visible spectroscopy, photoluminescence spectroscopy, and surface area measurements. The TX-capped ZnS nanopowders have a very good photocatalytic activity and high specific surface area, depending on the synthesis route; e.g. an azo dye solution is almost complete photobleached in only 60 min (a photocatalytic activity of 97.79%) using TX-capped ZnS nanopowder, with specific surface area of 191 m{sup 2}/g, and further a photocatalytic activity of 99.75% was achieved in 120 min. Based on the photocatalytic results, the ZnS nanopowders can be considered suitable catalysts for a green, very efficient and quick strategy for removing of organic pollutants from wastewaters. - Highlights: • Triton X-100 was used as surfactant in ZnS nanopowders synthesis by two methods. • Triton X-capped ZnS nanoparticles with high specific surface area were synthesized. • A very high capacity for bleaching an azo dye solution was evidenced. • Some of ZnS powders properties were crucially modified by the synthesis technique.

  2. The influence of Triton X-100 surfactant on the morphology and properties of zinc sulfide nanoparticles for applications in azo dyes degradation

    International Nuclear Information System (INIS)

    Dumbrava, Anca; Berger, Daniela; Prodan, Gabriel; Matei, Cristian; Moscalu, Florin; Diacon, Aurel

    2017-01-01

    Herein we report the synthesis, by two different routes, of ZnS nanoparticles capped with Triton X-100 (TX), which were characterized by X-ray diffraction, transmission electron microscopy, high resolution electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy, FTIR spectroscopy, UV–visible spectroscopy, photoluminescence spectroscopy, and surface area measurements. The TX-capped ZnS nanopowders have a very good photocatalytic activity and high specific surface area, depending on the synthesis route; e.g. an azo dye solution is almost complete photobleached in only 60 min (a photocatalytic activity of 97.79%) using TX-capped ZnS nanopowder, with specific surface area of 191 m 2 /g, and further a photocatalytic activity of 99.75% was achieved in 120 min. Based on the photocatalytic results, the ZnS nanopowders can be considered suitable catalysts for a green, very efficient and quick strategy for removing of organic pollutants from wastewaters. - Highlights: • Triton X-100 was used as surfactant in ZnS nanopowders synthesis by two methods. • Triton X-capped ZnS nanoparticles with high specific surface area were synthesized. • A very high capacity for bleaching an azo dye solution was evidenced. • Some of ZnS powders properties were crucially modified by the synthesis technique.

  3. Enhanced degradation of azo dye alizarin yellow R in a combined process of iron-carbon microelectrolysis and aerobic bio-contact oxidation.

    Science.gov (United States)

    Liang, Bin; Yao, Qian; Cheng, Haoyi; Gao, Shuhong; Kong, Fanying; Cui, Dan; Guo, Yuqi; Ren, Nanqi; Lee, Duu-Jong; Wang, Aijie

    2012-06-01

    With the aim of enhanced degradation of azo dye alizarin yellow R (AY) and further removal of the low-strength recalcitrant matter (LsRM) of the secondary effluent as much as possible, our research focused on the combination of aerobic bio-contact oxidation (ABO) with iron/carbon microelectrolysis (ICME) process. The combined ABO (with effective volume of 2.4 l) and ICME (with effectively volume of 0.4 l) process were studied with relatively short hydraulic retention time (HRT) of 4 or 6 h. At the HRT of 6 h with the reflux ratio of 1 and 2, the AY degradation efficiency in the final effluent was >96.5%, and the total organic carbon (TOC) removal efficiency were 69.86% and 79.44%, respectively. At the HRT of 4 h and the reflux ratio of 2, TOC removal efficiency and AY degradation efficiency were 73.94% and 94.89%, respectively. The ICME process obviously enhanced the total AY removal and the generated micromolecule acids and aldehydes then that wastewater backflow to the ABO where they were further biodegraded. The present research might provide the potential options for the advanced treatment azo dyes wastewater with short HRT and acceptable running costs.

  4. A magenta polypyrrole derivatised with Methyl Red azo dye: synthesis and spectroelectrochemical characterisation

    International Nuclear Information System (INIS)

    Almeida, Andresa K.A.; Dias, Jéssica M.M.; Santos, Diego P.; Nogueira, Fred A.R.; Navarro, Marcelo; Tonholo, Josealdo; Lima, Dimas J.P.; Ribeiro, Adriana S.

    2017-01-01

    Highlights: • A pyrrole (Py) derivative functionalised with methyl red (MRPy) was synthesised. • MRPy was polymerised electrochemically in LiClO_4/CH_3CN with BFEE. • Electrochromic properties of PMRPy and PPy doped with methyl red (PPy/MR) were compared. • Colour of the PMRPy changes from magenta to yellow depending on the pH. • PMRPy films might be applicable in optoelectronic devices or in pH sensors. - Abstract: A pyrrole derivative bearing 2-(4-dimethylaminophenylazo)benzoic acid, also known as Methyl Red (MR), was prepared by a simple synthetic route, and electropolymerised onto ITO/glass electrodes in (C_4H_9)_4NBF_4/CH_3CN in presence of boron trifluoride diethyl etherate (BFEE). Films of polypyrrole (PPy) and PPy doped with MR (PPy/MR) were also deposited onto ITO/glass in order to compare their electrochromic properties with the films of PPy derivatised with MR. Cyclic voltammogram of the poly[3-(N-pyrrolyl)propyl 2-(4-dimethylaminophenylazo)benzoate] (PMRPy) film displayed a redox pair with anodic peak potential (Epa) at ca. 0.53 V and cathodic peak potential (Epc) at 0.25 V vs. Ag/Ag"+, corresponding to the polymer p-doping, whilst the PPy/MR film shows capacitive behaviour with a redox pair in the cathodic region (Epa = −0.36 V and Epc = −0.62 V), similar to the PPy film (Epa = −0.10 V, and Epc = −0.15 V), and an anodic wave in the same potential range of that for PMRPy film. The electrochromic properties of the PMRPy film, such as chromatic contrast (Δ%T = 34.2%), switching time (τ = 10 s) and stability (Δ%T = 15% at the 100th cycle), were enhanced relative to the PPy/MR and PPy films. However, the colour of the PMRPy film changed from yellow (-0.8 V) to magenta (E = 1.0 V) in the first cycle and became light magenta at −0.8 V in the subsequent cycles. PMRPy films were also investigated in phosphate buffer solution (PBS, 2.0 ≤ pH ≤ 9.0) and after exposure to HCl vapour, in which the colour varied from magenta at pH = 2.0 to

  5. Photodegradation of polymer-dispersed perylene di-imide dyes

    Science.gov (United States)

    Tanaka, Nobuaki; Barashkov, Nikolay; Heath, Jerry; Sisk, Wade N.

    2006-06-01

    Polymer-dispersed perylene di-imide dye photodegradation is investigated by monitoring the fluorescence intensity as a function of 532 nm laser pulses. Anaerobically irradiated polymer-dye films exhibited an accelerated decrease in fluorescence intensity, which was partially recovered upon exposure to oxygen. Decelerated photodegradation rates were observed for perylene di-imide ethanol solutions upon the addition of a singlet oxygen quenching antioxidant. These observations suggest reversible photoreduction and type II photo-oxidation as important photodegradation mechanisms. Type II photo-oxidation for perylene red 532 nm irradiation is supported by a singlet oxygen quantum yield of 0.09±0.03, determined via detection of time-resolved O2 (a1Δg —> X3∑g-) infrared phosphorescence.

  6. Synthesis, characterization and degradation activity of Methyl orange Azo dye using synthesized CuO/α-Fe2O3 nanocomposite

    Directory of Open Access Journals (Sweden)

    Mohsen Mehdipour Ghazi

    2017-04-01

    Full Text Available This study investigated the photo-degradation of methyl orange (MO as a type of azo dye using a CuO/α-Fe2O3 nanocomposite. A CuO/α-Fe2O3 powder with a crystalline size in the range of 27-49 nm was successfully prepared using simple co-precipitation along with a sonication method. The characterization of the synthesized sample was done via XRD, FE-SEM, EDS, FTIR and DRS analyses. The Tauc equation revealed that the band gap of the nano composite in the direct mood was 2.05 ev, which is in the visible light range. The effect of operating factors containing dye concentration, photocatalyst dosage and pH on dye degradation efficiency was measured. Response Surface Method (RSM was employed to specify the parameter effects. The photocatalytic activity of the CuO/α-Fe2O3 nanocomposite was evaluated by degradation of MO under visible light irradiation. The results showed that the pH value played a very effective role in the dye degradation process efficiency. Also, the photocatalytic degradation of MO obtained was equal to 88.47% in the optimal values.

  7. Characterization of pore-expanded amino-functionalized mesoporous silicas directly synthesized with dimethyldecylamine and its application for decolorization of sulphonated azo dyes

    International Nuclear Information System (INIS)

    Yang Hong; Feng Qiyan

    2010-01-01

    With dimethyldecylamine (DMDA) as the expander, a new kind of pore-expanded amino-functionalized mesoporous silicas (PEAFMS) was directly synthesized under mild alkali condition. The characteristics of PEAFMS sample demonstrated that the presence of DMDA markedly augmented the average pore diameter (19.04 nm) and strongly enhanced its decolorization ability. Subsequently, acid mordant dark yellow GG (YGG) and reactive red violet X-2R (RVX) were chosen to assess its adsorption capacity for sulphonated azo dyes. The effect of initial pH was investigated and the decolorization mechanism was illuminated. Three isotherms were conducted and the goodness of fit increased as the following order: Freundlich < Langmuir < Redlich-Peterson. The maximum adsorption capacities of YGG and RVX onto PEAFMS were 1.967 and 0.957 mmol/g, respectively. Adsorption kinetic processes were better predicted by the pseudo-second-order rate equation than the pseudo-first-order one. Adsorption thermodynamic results suggested that the adsorption behavior of both dyes onto PEAFMS was spontaneous with the chemical nature. In addition, the regeneration of PEAFMS was proved to be feasible using NaOH as the strippant. After five cycles, PEAFMS still possessed a favorable adsorption capacity for dyes. It is safely concluded that PEAFMS could be a potential adsorbent for the dye removal from wastewater.

  8. Adsorption mechanism and kinetics of azo dye chemicals on oxide nanotubes: a case study using porous CeO{sub 2} nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Junshu; Wang, Jinshu, E-mail: wangjsh@bjut.edu.cn; Du, Yucheng; Li, Hongyi; Jia, Xinjian [Beijing University of Technology, School of Materials Science and Engineering (China)

    2016-07-15

    Metal oxide nanotubes are believed to be promising materials with adsorption functionality for water purification due to their synergistic effect of the overall microscale morphology for easy separation and nanoscale surface characters providing enough surface active absorption sites. This work shows the synthesis of uniform hierarchical porous CeO{sub 2} nanotubes via nanowire-directed templating method and describes the adsorption behavior of CeO{sub 2} nanotubes for a typical azo dye Congo red which has resistance to oxidation and decoloration in natural conditions. Fourier transform infrared spectroscopy spectra provided the evidence that Congo red was successfully coated on the surface of CeO{sub 2} nanotubes by both bidentate-type bridge link of Ce{sup 4+} cations from sulfonate SO{sub 3}{sup −} groups and the electrostatic attraction between the protonated surface generated by oxygen vacancies and dissociated sulfonate groups. The adsorption kinetic data fitted well to the pseudo-second-order kinetic equation, whereas the Langmuir isotherm equation exhibited better correlation with the experimental data. The calculated maximum adsorption capacity from the isothermal model was 362.32 mg/g. In addition, the prepared CeO{sub 2} nanotubes exhibited good recyclability and reusability as highly efficient adsorbents for Congo red removal after regeneration. These favorable performances enable the obtained CeO{sub 2} nanotubes to be promising materials for dye removal from aqueous solution.Graphical AbstractCeO{sub 2} nanotubes composed of crystallized nanoparticles exhibit well adsorption ability for a typical azo dye Congo red.

  9. Light harvesting by dye linked conducting polymers

    Energy Technology Data Exchange (ETDEWEB)

    Troensegaard Nielsen, K.

    2006-06-15

    The fact that the fossil fuel is finite and that the detrimental long-term effects of letting CO2 into our atmosphere exist, have created an enormous interest in developing new, cheap, renewable and less polluting energy resources. One of the most obvious abundant sources of energy in the solar system is the sun. Unfortunately the well developed silicon solar cells are very costly to produce. In an attempt to produce cheap and flexible solar cells, plastic solar cells have received a lot of attention in the last decades. There are still a lot of parameters to optimize if the plastic solar cell shall be able to compete with the silicon solar cells. One of the parameters is to ensure a high degree of charge carrier separation. Charge carrier separation can only happen at heterojunctions, which cover for example the interfaces between the polymers and the electrodes or the interface between an n-conductor and a p-conductor. The facts that the charge carrier separation only happens at the heterojunctions limits the thickness of the active layer in solar cells and thereby the effectiveness of the solar cells. In this project the charge carrier separation is attempted optimized by making plastic solar cells with a molecular heterojunction. The molecular heterojunction has been obtained by synthesizing a three domain super molecular assembly termed NPN. NPN consists of two poly[1-(2,5-dioctyltolanyl)ethynylene] chains (N-domains) coupled to the [10,20-bis(3,5-bistert-butylphenyl]-5,15-dibromoporphinato]zinc(II) (P-domain). It is shown that the N domains in NPN work as effective light harvesting antennas for the P domain and effectively transfer electrically generated excitons in the N domain to the P domain. Unfortunately the P domain does not separate the charge carriers but instead works as a charge carrier trap. This results in a performance of solar cells made of NPN that is much lower than the performance of solar cells made of pure poly[1-(2,5-dioctyltolanyl

  10. Optical, thermal and combustion properties of self-colored polyamide nanocomposites reinforced with azo dye surface modified ZnO nanoparticles

    Science.gov (United States)

    Hajibeygi, Mohsen; Shabanian, Meisam; Omidi-Ghallemohamadi, Mehrdad; Khonakdar, Hossein Ali

    2017-09-01

    New self-colored aromatic-polyamide (PA) nanocomposites containing azo and naphthalene chromophores were prepared with azo-dye surface-modified ZnO nanoparticles (SMZnO) using solution method in dimethylformamide. The X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) results showed the uniform distribution for ZnO nanoparticles in the PA matrix. The UV-vis spectra of PA/ZnO nanocomposites (PANC) showed a blue shift as well as reduction in absorbance intensities and the photoluminescence studies revealed that the increasing intensities of the violet emission in SMZnO loading. From thermo gravimetric analysis (TGA), the temperature at 10% mass loss (T10) increased from 291.8 °C to 387.6 °C for PANC containing 8 mass% of SMZnO, as well as the char yield enhanced significantly, which was about 23.5% higher than the neat PA. The peak heat release rate resulted from microscale combustion calorimeter (MCC), by 8 mass% loading of SMZnO, decreased about 56.9% lower than the neat PA.

  11. Azo dyes degradation using TiO2-Pt/graphene oxide and TiO2-Pt/reduced graphene oxide photocatalysts under UV and natural sunlight irradiation

    Science.gov (United States)

    Rosu, Marcela-Corina; Coros, Maria; Pogacean, Florina; Magerusan, Lidia; Socaci, Crina; Turza, Alexandru; Pruneanu, Stela

    2017-08-01

    The photocatalytic degradation of azo dyes with different structures (amaranth, sunset yellow and tartrazine) using TiO2-Pt nanoparticles (TPt), TiO2-Pt/graphene oxide (TPt-GO) and TiO2-Pt/reduced graphene oxide (TPt-rGO) composites were investigated in the presence of UV and natural sunlight irradiation. The composites were prepared by a combined chemical-thermal method and characterized by Transmission Electron Microscopy (TEM), X-ray powder diffraction (XRD), Infrared (FTIR) and UV-Vis spectroscopy. The modification of TiO2-Pt with graphene oxide shifted its optical absorption edge towards the visible region and increased its photocatalytic activity under UV and natural sunlight irradiation. The efficiency of catalysts on azo dyes degradation (in similar conditions) reached high values (above 99%) under sunlight conditions, proving the remarkable photocatalytic activities of obtained composites. TPt-GO nanocomposite exhibited higher photoactivity than TPt or TPt-rGO, demonstrating degradation efficiencies of 99.56% for amaranth, 99.15% for sunset yellow and 96.23% for tartrazine. The dye photodegradation process follows a pseudo-first-order kinetic with respect to the Langmuir-Hinshelwood reaction mechanism. A direct dependence between azo dyes degradation rate and chemical structure of dyes has been observed.

  12. An integrated (electro- and bio-oxidation) approach for remediation of industrial wastewater containing azo-dyes: Understanding the degradation mechanism and toxicity assessment.

    Science.gov (United States)

    Aravind, Priyadharshini; Selvaraj, Hosimin; Ferro, Sergio; Sundaram, Maruthamuthu

    2016-11-15

    A hybrid approach for the remediation of recalcitrant dye wastewater is proposed. The chlorine-mediated electrochemical oxidation of real textile effluents and synthetic samples (using Ti/IrO2-RuO2-TiO2 anodes), lead to discoloration by 92% and 89%, respectively, in 100min, without significant mineralization. The remediation was obtained through biodegradation, after removing the residual bio-toxic active chlorine species via sunlight exposition. Results show that the electrochemical discoloration enhances the effluent biodegradability with about 90% COD removal employing acclimatized naphthalene-degrading bacterial consortia, within 144h. Based on results obtained through FT-IR and GC-MS, it is likely that azo group stripping and oxidative cleavage of dyes occur due to the nucleophilic attack of active chlorine species during electro-oxidation. This leads to generation of aromatic intermediates which are further desulfonated, deaminated or oxidized only at their functional groups. These aromatic intermediates were mineralized into simpler organic acids and aldehydes by bacterial consortia. Phyto-toxicity trials on Vigna radiata confirmed the toxic nature of the untreated dye solutions. An increase in root and shoot development was observed with the electrochemically treated solutions, the same was higher in case of bio-treated solutions. Overall, obtained results confirm the capability of the proposed hybrid oxidation scheme for the remediation of textile wastewater. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Preparation and photocatalytic performance of Fe (III)-amidoximated PAN fiber complex for oxidative degradation of azo dye under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Yongchun, E-mail: dye@tjpu.edu.cn [Division of Textile Chemistry and Ecology, School of Textile Science and Engineering, Tianjin Polytechnic University, Tianjin 300160 (China); State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou, 350002 (China); Han, Zhenbang [Division of Textile Chemistry and Ecology, School of Textile Science and Engineering, Tianjin Polytechnic University, Tianjin 300160 (China); Liu, Chunyan [Division of Textile Chemistry and Ecology, School of Textile Science and Engineering, Tianjin Polytechnic University, Tianjin 300160 (China); State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou, 350002 (China); Du, Fang [Division of Textile Chemistry and Ecology, School of Textile Science and Engineering, Tianjin Polytechnic University, Tianjin 300160 (China)

    2010-04-15

    Polyacrylonitrile (PAN) fiber was modified with hydroxylamine hydrochloride to introduce amidoxime groups onto the fiber surface. These amidoxime groups were used to react with Fe (III) ions to prepare Fe (III)-amidoximated PAN fiber complex, which was characterized using SEM, XRD, FTIR, XPS, DMA, and DRS respectively. Then the photocatalytic activity of Fe-AO-PAN was evaluated in the degradation of a typical azo dye, C. I. Reactive Red 195 in the presence of H{sub 2}O{sub 2} under visible light irradiation. Moreover, the effect of the Fe content of Fe-AO-PAN on dye degradation was also investigated. The results indicated that Fe (III) ions can crosslink between the modified PAN fiber chains by the coordination of Fe (III) ions with the amino nitrogen atoms and hydroxyl oxygen atoms of the amidoximation groups to form Fe (III)-amidoximated PAN fiber complex, and the Fe content of which is mainly determined by Fe (III) ions and amidoximation groups. Fe (III)-amidoximated PAN fiber complex is found to be activated in the visible light region. Moreover, Fe (III)-amidoximated PAN fiber complex shows the catalytic activity for dye degradation by H{sub 2}O{sub 2} at pH = 6.0 in the dark, and can be significantly enhanced by increasing light irradiation and Fe content, therefore, it can be used as a new heterogeneous Fenton photocatalyst for the effective decomposition of the dye in water. In addition, ESR spectra confirm that Fe (III)-amidoximated PAN fiber complex can generate more {center_dot}OH radicals from H{sub 2}O{sub 2} under visible light irradiation, leading to dye degradation. A possible mechanism of photocatalysis is proposed.

  14. Removal of azo dye using Fenton and Fenton-like processes: Evaluation of process factors by Box-Behnken design and ecotoxicity tests.

    Science.gov (United States)

    Fernandes, Neemias Cintra; Brito, Lara Barroso; Costa, Gessyca Gonçalves; Taveira, Stephânia Fleury; Cunha-Filho, Marcílio Sérgio Soares; Oliveira, Gisele Augusto Rodrigues; Marreto, Ricardo Neves

    2018-06-06

    The conventional treatment of textile effluents is usually inefficient in removing azo dyes and can even generate more toxic products than the original dyes. The aim of the present study was to optimize the process factors in the degradation of Disperse Red 343 by Fenton and Fenton-like processes, as well as to investigate the ecotoxicity of the samples treated under optimized conditions. A Box-Behnken design integrated with the desirability function was used to optimize dye degradation, the amount of residual H 2 O 2 [H 2 O 2residual ], and the ecotoxicity of the treated samples (lettuce seed, Artemia salina, and zebrafish in their early-life stages). Dye degradation was affected only by catalyst concentration [Fe] in both the Fenton and Fenton-like processes. In the Fenton reaction, [H 2 O 2residual ] was significantly affected by initial [H 2 O 2 ] and its interaction with [Fe]; however, in the Fenton-like reaction, it was affected by initial [H 2 O 2 ] only. A. salina mortality was affected by different process factors in both processes, which suggests the formation of different toxic products in each process. The desirability function was applied to determine the best process parameters and predict the responses, which were confirmed experimentally. Optimal conditions facilitated the complete degradation of the dye without [H 2 O 2residual ] or toxicity for samples treated with the Fenton-like process, whereas the Fenton process induced significant mortality for A. salina. Results indicate that the Fenton-like process is superior to the Fenton reaction to degrade Disperse Red 343. Copyright © 2018 Elsevier B.V. All rights reserved.

  15. Compósitos de poli(álcool vinílico contendo hidroxissais lamelares de zinco, intercalados com corantes aniônicos azo (tropaeolina 0 e tropaeolina 00 Poly(vinyl alcohol composites containing layered hydroxide salts, intercalated with anionic azo dyes (tropaeolin 0 and tropaeolin 0

    Directory of Open Access Journals (Sweden)

    Marlon Luiz Neves da Silva

    2013-01-01

    Full Text Available Hidroxissais lamelares de zinco foram intercalados com corantes aniônicos azo, obtendo-se pigmentos de coloração laranja. Os materiais foram caracterizados por difração de raios X (XRD, espectroscopia vibracional na região do infravermelho com transformada de Fourier (FTIR, análise térmica (TGA/DTA/DSC e espectroscopia fotoeletrônica de raios X (XPS. Após caracterização, os pigmentos lamelares foram dispersos em uma matriz de poli(álcool vinílico - PVA, em concentrações variáveis, em relação à massa de PVA. Filmes homogêneos, transparentes e coloridos foram obtidos pelo método de "casting" úmido e mantidos em dessecador em umidade controlada de 65 % por uma semana e avaliados quanto às suas propriedades mecânicas. Devido às diferentes polaridades dos ânions intercalados, diferentes comportamentos foram observados para os pigmentos quando utilizados como cargas em PVA. Esse trabalho abre uma frente de pesquisas na utilização de hidroxissais lamelares intercalados com corantes aniônicos, como cargas alternativas em materiais compósitos poliméricos.Layered zinc hydroxide salts were intercalated with anionic azo dyes, obtaining orange pigments. The materials were characterized by X-ray diffraction (XRD, Fourier Transform Infrared spectroscopy (FTIR, thermal analysis (TGA/DTA/DSC and X-ray photoelectron spectroscopy (XPS. After characterization, the layered pigments were dispersed into a matrix of poly(vinyl alcohol - PVA, in variable concentrations, in relation to the PVA mass. Homogeneous, transparent and colorful films were obtained by wet casting method and kept in a desiccator at 65% of humidity for one week and evaluated in relation to their mechanical properties. Owing to the different intercalated anions polarities, different behaviors were observed for both pigments when used as fillers in PVA. This work opens a research front in the utilization of layered hydroxide salt intercalated with anionic dyes, as

  16. Single mode dye-doped polymer photonic crystal lasers

    International Nuclear Information System (INIS)

    Christiansen, Mads B; Buß, Thomas; Smith, Cameron L C; Petersen, Sidsel R; Jørgensen, Mette M; Kristensen, Anders

    2010-01-01

    Dye-doped polymer photonic crystal (PhC) lasers fabricated by combined nanoimprint and photolithography are studied for their reproducibility and stability characteristics. We introduce a phase shift in the PhC lattice that substantially improves the yield of single wavelength emission. Single mode emission and reproducibility of laser characteristics are important if the lasers are to be mass produced in, e.g., optofluidic sensor chips. The fabrication yield is above 85% with highly reproducible wavelengths (within 0.5%), and the temperature dependence on the wavelength is found to be −0.045 or −0.066 nm K -1 , depending on the material

  17. Single mode dye-doped polymer photonic crystal lasers

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Buss, Thomas; Smith, Cameron

    2010-01-01

    Dye-doped polymer photonic crystal (PhC) lasers fabricated by combined nanoimprint and photolithography are studied for their reproducibility and stability characteristics. We introduce a phase shift in the PhC lattice that substantially improves the yield of single wavelength emission. Single mode...... emission and reproducibility of laser characteristics are important if the lasers are to be mass produced in, e. g., optofluidic sensor chips. The fabrication yield is above 85% with highly reproducible wavelengths (within 0.5%), and the temperature dependence on the wavelength is found to be -0.045 or -0...

  18. An integrated (electro- and bio-oxidation) approach for remediation of industrial wastewater containing azo-dyes: Understanding the degradation mechanism and toxicity assessment

    International Nuclear Information System (INIS)

    Aravind, Priyadharshini; Selvaraj, Hosimin; Ferro, Sergio; Sundaram, Maruthamuthu

    2016-01-01

    Highlights: • Firstly, the mediated electro-oxidation allows rapid discoloration of the effluent. • Cost effective sunlight-mediated removal of bio-toxic active chlorine species. • Electrochemical pretreatment enhances the biodegradability of textile wastewater. • About 90% COD removal was achieved by a subsequent biodegradation. • By-products from degradation of dyes have shown to be ecofriendly and non-toxic. - Abstract: A hybrid approach for the remediation of recalcitrant dye wastewater is proposed. The chlorine-mediated electrochemical oxidation of real textile effluents and synthetic samples (using Ti/IrO_2-RuO_2-TiO_2 anodes), lead to discoloration by 92% and 89%, respectively, in 100 min, without significant mineralization. The remediation was obtained through biodegradation, after removing the residual bio-toxic active chlorine species via sunlight exposition. Results show that the electrochemical discoloration enhances the effluent biodegradability with about 90% COD removal employing acclimatized naphthalene-degrading bacterial consortia, within 144 h. Based on results obtained through FT-IR and GC–MS, it is likely that azo group stripping and oxidative cleavage of dyes occur due to the nucleophilic attack of active chlorine species during electro-oxidation. This leads to generation of aromatic intermediates which are further desulfonated, deaminated or oxidized only at their functional groups. These aromatic intermediates were mineralized into simpler organic acids and aldehydes by bacterial consortia. Phyto-toxicity trials on Vigna radiata confirmed the toxic nature of the untreated dye solutions. An increase in root and shoot development was observed with the electrochemically treated solutions, the same was higher in case of bio-treated solutions. Overall, obtained results confirm the capability of the proposed hybrid oxidation scheme for the remediation of textile wastewater.

  19. An integrated (electro- and bio-oxidation) approach for remediation of industrial wastewater containing azo-dyes: Understanding the degradation mechanism and toxicity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Aravind, Priyadharshini, E-mail: priya.bdu07@gmail.com [Corrosion and Materials Protection Division (CMPD), CSIR—Central electrochemical research institute (CECRI), Karaikudi 630 003 (India); Selvaraj, Hosimin [Corrosion and Materials Protection Division (CMPD), CSIR—Central electrochemical research institute (CECRI), Karaikudi 630 003 (India); Ferro, Sergio [Ecas4 Australia, Unit 8, 1 London Road, Mile End, South Australia 5031 (Australia); Sundaram, Maruthamuthu [Corrosion and Materials Protection Division (CMPD), CSIR—Central electrochemical research institute (CECRI), Karaikudi 630 003 (India)

    2016-11-15

    Highlights: • Firstly, the mediated electro-oxidation allows rapid discoloration of the effluent. • Cost effective sunlight-mediated removal of bio-toxic active chlorine species. • Electrochemical pretreatment enhances the biodegradability of textile wastewater. • About 90% COD removal was achieved by a subsequent biodegradation. • By-products from degradation of dyes have shown to be ecofriendly and non-toxic. - Abstract: A hybrid approach for the remediation of recalcitrant dye wastewater is proposed. The chlorine-mediated electrochemical oxidation of real textile effluents and synthetic samples (using Ti/IrO{sub 2}-RuO{sub 2}-TiO{sub 2} anodes), lead to discoloration by 92% and 89%, respectively, in 100 min, without significant mineralization. The remediation was obtained through biodegradation, after removing the residual bio-toxic active chlorine species via sunlight exposition. Results show that the electrochemical discoloration enhances the effluent biodegradability with about 90% COD removal employing acclimatized naphthalene-degrading bacterial consortia, within 144 h. Based on results obtained through FT-IR and GC–MS, it is likely that azo group stripping and oxidative cleavage of dyes occur due to the nucleophilic attack of active chlorine species during electro-oxidation. This leads to generation of aromatic intermediates which are further desulfonated, deaminated or oxidized only at their functional groups. These aromatic intermediates were mineralized into simpler organic acids and aldehydes by bacterial consortia. Phyto-toxicity trials on Vigna radiata confirmed the toxic nature of the untreated dye solutions. An increase in root and shoot development was observed with the electrochemically treated solutions, the same was higher in case of bio-treated solutions. Overall, obtained results confirm the capability of the proposed hybrid oxidation scheme for the remediation of textile wastewater.

  20. Azo polymers with electronical push and pull structures prepared via RAFT polymerization and its photoinduced birefringence behavior

    Directory of Open Access Journals (Sweden)

    2008-08-01

    Full Text Available Two methacrylate monomers containing azo and electronical push and pull structure, e.g. 2-Methyl-acrylic-acid-2-{[4-(4-cyano-phenylazo-3-methyl-phenyl]-ethyl-amino-ethyl ester (MACP with cyano substituted and 2-Methylacrylic-acid-2-{ethyl-[4-(4-methoxy-phenylazo-3-methyl-phenyl]-amino}-ethyl ester (MAMP with methoxy substituted, were synthesized and polymerized using 2-cyanoprop-2-yl dithiobenzoate (CPDB as chain transfer agent and 2,2'-azobisisobutyronitrile (AIBN as initiator. The results showed that the polymerization displayed characteristics of ‘living’/controlled free radical polymerization. Thus, the obtained polymers, polyMACP (pMACP and polyMAMP (pMAMP, had controlled molecular weights and narrow molecular weights distribution. The chain extension experiments of pMACP and pMAMP using styrene as the second monomer were successfully carried out. The photo-induced trans-cis-trans isomerization kinetic of pMACP and pMAMP in chloroform solution were described. Marked differences in rate for the trans-cis and cis-trans isomerization of pMACP and pMAMP were observed in chloroform solution due to the different electronic effects in these two polymers. Photoinduced birefringence and surface relief grating (SRG of the pMACP and pMAMP were investigated in thin film state.

  1. Hydrogen bonding intermolecular effect on electro-optical response of doped 6PCH nematic liquid crystal with some azo dyes

    Science.gov (United States)

    Kiani, S.; Zakerhamidi, M. S.; Tajalli, H.

    2016-05-01

    Previous studies on the electro-optical responses of dye-doped liquid crystal have shown that dopant material have a considerable effect on their electro-optical responses. Despite the studies carried out on electro-optical properties of dye-doped liquid crystal, no attention has been paid to study of the interaction and structural effects in this procedure. In this paper, linear dyes and with similar structure were selected as dopants. The only difference in used dyes is the functional groups in their tails. So, doping of these dyes into liquid crystals determines the influence of interaction type on electro-optical behaviours of the doped systems. Therefore, in this work, two aminoazobenzene (;A-dye;: hydrogen bond donor) and dimethyl-aminoazobenzene (;B-dye;) dyes with different compositional percentages in liquid crystal host were used. Electro-optical Kerr behaviour, the pre-transition temperature and third order nonlinear susceptibility were investigated. The obtained results effectively revealed that type of interactions between the dye and liquid crystal is determinative of behavioral difference of doped system, compared to pure liquid crystal. Also, pre-transitional behaviour and thereupon Kerr electro-optical responses were affected by formed interactions into doped systems. In other words, it will be shown that addition of any dopants in liquid crystal, regardless of the nature of interactions, cannot cause appropriate electro-optical responses. In fact, type of dye, nature of interactions between dopant and liquid crystalline host as well as concentration of dye are the key factors in selecting the appropriate liquid crystal and dopant dye.

  2. Impacto dos mediadores redox na remoção de cor de corantes azo e antraquinônico por lodo granular anaeróbio sob condições mesofílicas e termofílicas Impact of redox mediators on colour removal of azo and anthraquinone dyes by anaerobic granular sludge under mesophilic and thermophilic conditions

    Directory of Open Access Journals (Sweden)

    André Bezerra dos Santos

    2007-03-01

    Full Text Available Investigou-se o efeito de diferentes mediadores redox (MR na remoção de cor de corantes azo e antraquinônico pelo uso de lodo granular anaeróbio sob condições mesofílicas (30ºC e termofílicas (55ºC. Comprovou-se em experimento em batelada que a adição de concentrações catalíticas de MR pode ter um efeito marcante nas taxas de descoloração do corante azo Reactive Red 2 (RR2, mas o mesmo comportamento não pode ser obtido com o corante antraquinônico Reactive Blue 5 (RB5. Entretanto, com ambos os corantes, o simples aumento da temperatura de incubação para condições termofílicas fez acelerar consideravelmente os processos de descoloração, comparados com condições mesofílicas. Por exemplo, a constante de primeira ordem "k" da redução dos corantes RR2 e RB5, foi aumentada em 6,2 e 11 vezes, respectivamente, à 55ºC quando comparado com 30ºC. Por fim, comprovou-se em experimentos de fluxo contínuo, a boa performance do tratamento termofílico na descoloração redutiva de corantes azo.The effect of different redox mediators (RM on colour removal of azo and anthraquinone dyes was investigated with anaerobic granular sludge under mesophilic (30ºC and thermophilic (55ºC conditions. Batch experiments revealed that an addition of catalytic concentrations of RM provided a remarkable effect on the decolourisation rates of the azo dye Reactive Red 2 (RR2, but the same effect could not be obtained with the anthraquinone dye Reactive Blue 5 (RB5. Nevertheless, for both dyes, the temperature increase to thermophilic conditions was an effective strategy to considerably accelerate the decolourisation process compared to mesophilic conditions. For instance, the first-order rate constant "k" of RR2 and RB5 reduction, was increased in 6.2 and 11-fold, respectively, at 55ºC in comparison with 30ºC. Such an effect of the temperature on the reductive decolourisation of azo dye was also verified in continuous flow experiments.

  3. Novel acid mono azo dye compound: Synthesis, characterization, vibrational, optical and theoretical investigations of 2-[(E)-(8-hydroxyquinolin-5-yl)-diazenyl]-4,5-dimethoxybenzoic acid

    Science.gov (United States)

    Saçmacı, Mustafa; Çavuş, Hatice Kanbur; Arı, Hatice; Şahingöz, Recep; Özpozan, Talat

    2012-11-01

    Novel acid mono azo dye, 2-[(E)-(8-hydroxyquinolin-5yl)-diazenyl]-4,5-dimethoxybenzoic acid (HQD), was synthesized by coupling diazonium salt solution of 2-amino-4,5-dimethoxybenzoic acid (DMA) with 8-hydroxyquinoline (HQ). This dye was characterized by UV-vis, IR & Raman, 1H and 13C NMR spectroscopic techniques and elemental analysis. The normal coordinate analysis of HQD was also performed to assign each band in vibrational spectra. DFT (B3LYP and B3PW91) calculations were employed to optimize the geometry, to interpret NMR spectra, to calculate and to determine the stable tautomeric structure of the compound. Natural Bond Orbital (NBO) analysis was performed to investigate intramolecular interactions. The vibrational spectral data obtained from solid phase IR & Raman spectra were assigned based on the results of the theoretical calculations. UV-vis spectroscopic technique was employed to obtain the optical band gap of HQD. The analysis of the optical absorption data revealed the existence of direct and indirect transitions in the optical band gaps. The optical band gaps of HQD have been found 1.95 and 1.90 eV for direct and indirect transitions, respectively.

  4. Enhanced accumulation and visible light-assisted degradation of azo dyes in poly(allylamine hydrochloride)-modified mesoporous silica spheres

    International Nuclear Information System (INIS)

    Tao Xia; Liu Bing; Hou Qian; Xu Hui; Chen Jianfeng

    2009-01-01

    A new route for the economic and efficient treatment of azo dye pollutants is reported, in which surface-modified organic-inorganic hybrid mesoporous silica (MS) spheres were chosen as microreactors for the accumulation and subsequent photodegradation of pollutants in defined regions. The surface-modified silica materials were prepared by anchoring the polycationic species such as poly(allylamine hydrochloride) on MS spheres via a simple wet impregnation method. The as-synthesized spheres with well-defined porous structures exhibited 15 times of accumulating capacity for orange II and Congo red compared to that of the pure MS spheres. Diffuse reflectance UV-vis spectroscopy and confocal laser scanning microscopy demonstrated that the accumulated orange II and CR in defined MS spheres were rapidly degraded in the presence of Fenton reagent under visible radiation. Kinetics analysis in recycling degradation showed that the as-synthesized materials might be utilized as environment-friendly preconcentrators/microreactors for the remediation of dye wastewater

  5. Treatment of a non-azo dye aqueous solution by CWAO in continuous reactor using a Ni catalyst derived from hydrotalcite-like precursor.

    Science.gov (United States)

    Vallet, Ana; Besson, Michèle; Ovejero, Gabriel; García, Juan

    2012-08-15

    Catalytic wet air oxidation (CWAO) of a Basic Yellow 11 (BY11) aqueous solution, chosen as a model of a hardly biodegradable non-azo dye was carried out in a continuous-flow trickle-bed reactor, using nickel supported over hydrotalcite precursor calcined at 550°C. An increase in the reaction temperature (120-180°C), and a decrease in dye concentration (1000-3000 ppm) or liquid flow rate (0.1-0.7 mL min(-1)) enhanced the CWAO performance in a 30 and 19% for the variation of the temperature and concentration respectively. After a small leaching observed within the first hours, the catalyst proved to be very stable during the 65-day reaction. The CWAO process was found to be very efficient, achieving BY11 conversion up to 95% and TOC conversion up to 85% at 0.1 mL min(-1) and 180°C under 5 MPa air. Copyright © 2012 Elsevier B.V. All rights reserved.

  6. Photoassisted electrochemical recirculation system with boron-doped diamond anode and carbon nanotubes containing cathode for degradation of a model azo dye

    International Nuclear Information System (INIS)

    Vahid, Behrouz; Khataee, Alireza

    2013-01-01

    In this research work, a photoassisted electrochemical system under recirculation mode and with UV irradiation was designed for treatment of C.I. Acid Blue 92 (AB92) as a model anionic azo dye in aqueous solution. Degradation experiments were carried out with boron-doped diamond (BDD) anode and carbon nanotubes-polytetrafluoroethylene (CNTs-PTFE) cathode in the presence of sulfate as an electrolyte. A comparative study of AB92 degradation by photolysis, electrochemical oxidation and photoassisted electrochemical processes after 45 min of treatment demonstrated that degradation efficiency was 27.89, 37.65 and 95.86%, respectively. Experimental data revealed that the degradation rate of AB92 in all of the processes obeyed pseudo-first-order kinetics and application of photoassisted electrochemical system reduced electrical energy per order (E EO ), considerably. Degradation efficiency of photoassisted electrochemical process enhanced by increasing applied current and flow rate values, but vice versa trend was observed for initial dye concentration and an optimum amount of 6 was obtained for initial pH. The TOC measurement results demonstrated that 93.24% of organic substrates were mineralized after 120 min of photoassisted electrochemical process and GC–Mass analysis was performed for identification of degradation intermediates

  7. Potential of the aquatic fern Azolla filiculoides in biodegradation of an azo dye: modeling of experimental results by artificial neural networks.

    Science.gov (United States)

    Khataee, A R; Movafeghi, A; Vafaei, F; Lisar, S Y Salehi; Zarei, M

    2013-01-01

    The potential of an aquatic fern, Azolla filiculoides, in phytoremediation of a mono azo dye solution, C.I. Acid Blue 92 (AB92), was studied. The effects of operational parameters such as reaction time, initial dye concentration, fern fresh weight, pH, temperature and reusability of the fern on biodegradation efficiency were investigated. The intermediate compounds produced by biodegradation process were analyzed using GC-MS analysis. An artificial neural network (ANN) model was developed to predict the biodegradation efficiency. The findings indicated that ANN provides reasonable predictive performance (R2 = 0.961). The effects of AB92 solutions (10 and 20 mg L(-1)) on growth, chlorophylls and carotenoids content, activity of antioxidant enzymes such as superoxide dismutase, peroxidase and catalase and formation of malondialdehyde were analyzed. AB92 generally showed inhibitory effects on the growth. Moreover, photosynthetic pigments in the fronds significantly decreased in the treatments. An increase was detected for lipid peroxidation and antioxidant enzymes activity, suggesting that AB92 caused reactive oxygen species production in Azolla fronds, which were scavenged by induced activities of antioxidant enzymes.

  8. New self-assembled material based on Ru nanoparticles and 4-sulfocalix[4]arene as an efficient and recyclable catalyst for reduction of brilliant yellow azo dye in water: a new model catalytic reaction

    Energy Technology Data Exchange (ETDEWEB)

    Rambabu, Darsi; Pradeep, Chullikkattil P.; Dhir, Abhimanew, E-mail: abhimanew@iitmandi.ac.in [Indian Institute of Technology (India)

    2016-12-15

    New self-assembled material (Ru@SC) with ruthenium nanoparticles (Ru NPs) and 4-sulfocalix[4]arene (SC) is synthesized in water at room temperature. Ru@SC is characterized by thermal gravimetric analysis, FT-IR, powder x-ray diffraction, TEM and SEM analysis. The size of Ru nanoparticles in the self-assembly is approximately 5 nm. The self-assembled material Ru@SC shows an efficient catalytic reduction of toxic ‘brilliant yellow’ (BY) azo dye. The reduced amine products were successfully separated and confirmed by single-crystal XRD, NMR and UV-Vis spectroscopy. Ru@SC showed a better catalytic activity in comparison with commercial catalysts Ru/C (ruthenium on charcoal 5 %) and Pd/C (palladium on charcoal 5 and 10 %). The catalyst also showed a promising recyclability and heterogeneous nature as a catalyst for reduction of ‘BY’ azo dye.

  9. Fabrication of Microcapsules for Dye-Doped Polymer-Dispersed Liquid Crystal-Based Smart Windows.

    Science.gov (United States)

    Kim, Mingyun; Park, Kyun Joo; Seok, Seunghwan; Ok, Jong Min; Jung, Hee-Tae; Choe, Jaehoon; Kim, Do Hyun

    2015-08-19

    A dye-doped polymer-dispersed liquid crystal (PDLC) is an attractive material for application in smart windows. Smart windows using a PDLC can be operated simply and have a high contrast ratio compared to those of other devices that employed photochromic or thermochromic material. However, in conventional dye-doped PDLC methods, dye contamination can cause problems and has a limited degree of commercialization of electric smart windows. Here, we report on an approach to resolve dye-related problems by encapsulating the dye in monodispersed capsules. By encapsulation, a fabricated dye-doped PDLC had a contrast ratio of >120 at 600 nm. This fabrication method of encapsulating the dye in a core-shell structured microcapsule in a dye-doped PDLC device provides a practical platform for dye-doped PDLC-based smart windows.

  10. Morphological appearances and photo-controllable coloration of dye-doped cholesteric liquid crystal/polymer coaxial microfibers fabricated by coaxial electrospinning technique.

    Science.gov (United States)

    Lin, Jia-De; Chen, Che-Pei; Chen, Lin-Jer; Chuang, Yu-Chou; Huang, Shuan-Yu; Lee, Chia-Rong

    2016-02-08

    This study systematically investigates the morphological appearance of azo-chiral dye-doped cholesteric liquid crystal (DDCLC)/polymer coaxial microfibers obtained through the coaxial electrospinning technique and examines, for the first time, their photocontrollable reflection characteristics. Experimental results show that the quasi-continuous electrospun microfibers can be successfully fabricated at a high polymer concentration of 17.5 wt% and an optimum ratio of 2 for the feeding rates of sheath to core materials at 25 °C and a high humidity of 50% ± 2% in the spinning chamber. Furthermore, the optical controllability of the reflective features for the electrospun fibers is studied in detail by changing the concentration of the azo-chiral dopant in the core material, the UV irradiation intensity, and the core diameter of the fibers. Relevant mechanisms are addressed to explain the optical-control behaviors of the DDCLC coaxial fibers. Considering the results, optically controllable DDCLC coaxial microfibers present potential applications in UV microsensors and wearable smart textiles or swabs.

  11. Magnetic polymer microcapsules loaded with Nile Red fluorescent dye

    Science.gov (United States)

    Bartel, Marta; Wysocka, Barbara; Krug, Pamela; Kępińska, Daria; Kijewska, Krystyna; Blanchard, Gary J.; Kaczyńska, Katarzyna; Lubelska, Katarzyna; Wiktorska, Katarzyna; Głowala, Paulina; Wilczek, Marcin; Pisarek, Marcin; Szczytko, Jacek; Twardowski, Andrzej; Mazur, Maciej

    2018-04-01

    Fabrication of multifunctional smart vehicles for drug delivery is a fascinating challenge of multidisciplinary research at the crossroads of materials science, physics and biology. We demonstrate a prototypical microcapsule system that is capable of encapsulating hydrophobic molecules and at the same time reveals magnetic properties. The microcapsules are prepared using a templated synthesis approach where the molecules to be encapsulated (Nile Red) are present in the organic droplets that are suspended in the polymerization solution which also contains magnetic nanoparticles. The polymer (polypyrrole) grows on the surface of organic droplets encapsulating the fluorescent dye in the core of the formed microcapsule which incorporates the nanoparticles into its wall. For characterization of the resulting structures a range of complementary physicochemical methodology is used including optical and electron microscopy, magnetometry, 1H NMR and spectroscopy in the visible and X-ray spectral ranges. Moreover, the microcapsules have been examined in biological environment in in vitro and in vivo studies.

  12. Control of gain in conjugated polymers and perylene dyes

    International Nuclear Information System (INIS)

    Sheridan, A.

    2001-03-01

    This thesis presents an investigation into the factors which control the gain and amplification properties in conjugated materials. Conjugated polymers and perylene dyes are highly fluorescent, are easy to process into thin films, and exhibit strong amplification over a broad gain bandwidth making them ideal for use in lasers and amplifiers. The stimulated emission created when thin films of the red emitting polymer poly(2-methoxy-5-(2'-ethylhexyloxy)-p-phenylenvinylene) (MEH-PPV) were photoexcited with high energy laser pulses was investigated. This was characterised by a dramatic narrowing of the emission spectrum which has been assigned to amplified spontaneous emission (ASE). The emission was found to have a gaussian profile and the gain coefficient was found to be 4 cm -1 . The temperature dependence of the absorption, photoluminescence and ASE of films of MEH-PPV was measured. The effect of film morphology on the photophysical properties was investigated by using films cast from two spinning solvents, chlorobenzene (CB) and tetrahydrofuran (THF). Film morphology was found to greatly affect the temperature dependence. A particularly important property is the spectral position of the ASE and the factors which affect it. By controlling the film thickness close to the cut-off thickness for waveguiding in the polymer film it was shown that the peak position of the ASE could be tuned by 31 nm. Modelling of the waveguide modes in the polymer films was used to explain this effect. The cut-off wavelength for each film was measured and good agreement with the theory was found. In order to investigate ways in which energy transfer could be used to control the emission, two perylene dyes were used as a donor-acceptor pair in a host matrix of poly methymethacralate (PMMA). The position of the ASE was found to depend on the acceptor concentration. Measurements of the photoluminescence quantum yield and time-resolved luminescence measurements showed that the energy transfer

  13. Enhanced solar light photodegradation of brilliant black bis-azo dye in aqueous solution by F, Sm3+ codoped TiO2

    Science.gov (United States)

    Mukonza, Sabastian S.; Nxumalo, Edward N.; Mamba, Bhekie B.; Mishra, Ajay K.

    2017-05-01

    This research focuses on improving the photocatalytic efficiency of TiO2 during the photo-mineralisation of brilliant black (BN) bis-azo dye pollutant in aqueous solution. This was achieved by improving the visible light activity of TiO2 photocatalyst semiconductor through co-doping of fluorine (F) and trivalent samarium ions (Sm3+) into a TiO2 matrix using a modified sol-gel synthesis method. Structural, morphological, and textural properties were evaluated using ultra-violet /visible spectroscopy (UV-visible), Raman spectroscopy, scanning electron microscopy coupled to energy dispersive X-ray spectroscopy (SEM/EDX) and X-ray diffraction spectroscopy (XRD). Photocatalytic and degradation efficiencies were assessed by decolourisation of BN dye in aqueous solution. Complete degradation of BN was attained after an irradiation time of 3 h using F, Sm3+-TiO2 (0.6% Sm3+) compared to 73.4% achieved using pristine TiO2. Pseudo first order kinetics rate constants (Ka) were 2.73×10-2 and 6.6×10-3 min-1 for Sm3+-TiO2 (0.6%Sm3+) and pristine TiO2, respectively, which translates to a remarkably high enhancement factor of 4. The results obtained established that doping of TiO2 by F and Sm3+ enhances the photocatalytic performance of TiO2 during solar light radiation which enables the utilisation of freely available and clean solar energy.

  14. Characterization and performance of carbonaceous materials obtained from exhausted sludges for the anaerobic biodecolorization of the azo dye Acid Orange II

    Energy Technology Data Exchange (ETDEWEB)

    Athalathil, S.; Stüber, F.; Bengoa, C.; Font, J. [Departament d’Enginyeria Quimica, ETSEQ, Universitat Rovira i Virgili, Av. Paisos Catalans 26, 43007 Tarragona, Catalunya (Spain); Fortuny, A. [Departament d’Enginyeria Quimica, EPSEVG, Universitat Politecnica de Catalunya, Av. Victor Balaguer s/n, 08800 Vilanova i la Geltru, Catalunya (Spain); Fabregat, A., E-mail: azael.fabregat@urv.cat [Departament d’Enginyeria Quimica, ETSEQ, Universitat Rovira i Virgili, Av. Paisos Catalans 26, 43007 Tarragona, Catalunya (Spain)

    2014-02-01

    Graphical abstract: - Highlights: • Carbonaceous materials were prepared from exhausted sludge materials. • High surface area and good physicochemical properties were achieved. • Utilization of waste sludge materials and mixed anaerobic cultures were used in a continuous anaerobic UPBR system (upflow packed bed biological reactor). • Effective treatment of dye contaminated wastewater in a cheapest and environmental friendly method was demonstrated. - Abstract: This work presents the preliminary study of new carbonaceous materials (CMs) obtained from exhausted sludge, their use in the heterogeneous anaerobic process of biodecolorization of azo dyes and the comparison of their performance with one commercial active carbon. The preparation of carbonaceous materials was conducted through chemical activation and carbonization. Chemical activation was carried out through impregnation of sludge-exhausted materials with ZnCl{sub 2} and the activation by means of carbonization at different temperatures (400, 600 and 800 °C). Their physicochemical and surface characteristics were also investigated. Sludge based carbonaceous (SBC) materials SBC400, SBC600 and SBC800 present values of 13.0, 111.3 and 202.0 m{sup 2}/g of surface area. Biodecolorization levels of 76% were achieved for SBC600 and 86% for SBC800 at space time (τ) of 1.0 min, similar to that obtained with commercial activated carbons in the continuous anaerobic up-flow packed bed reactor (UPBR). The experimental data fit well to the first order kinetic model and equilibrium data are well represented by the Langmuir isotherm model. Carbonaceous materials show high level of biodecolorization even at very short space times. Results indicate that carbonaceous materials prepared from sludge-exhausted materials have outstanding textural properties and significant degradation capacity for treating textile effluents.

  15. Using Polarized Spectroscopy to Investigate Order in Thin-Films of Ionic Self-Assembled Materials Based on Azo-Dyes

    Science.gov (United States)

    Ahmad, Mariam; Andersen, Frederik; Brend Bech, Ári; Bendixen, H. Krestian L.; Nawrocki, Patrick R.; Bloch, Anders J.; Bora, Ilkay; Bukhari, Tahreem A.; Bærentsen, Nicolai V.; Carstensen, Jens; Chima, Smeeah; Colberg, Helene; Dahm, Rasmus T.; Daniels, Joshua A.; Dinckan, Nermin; El Idrissi, Mohamed; Erlandsen, Ricci; Førster, Marc; Ghauri, Yasmin; Gold, Mikkel; Hansen, Andreas; Hansen, Kenn; Helmsøe-Zinck, Mathias; Henriksen, Mathias; Hoffmann, Sophus V.; Hyllested, Louise O. H.; Jensen, Casper; Kallenbach, Amalie S.; Kaur, Kirandip; Khan, Suheb R.; Kjær, Emil T. S.; Kristiansen, Bjørn; Langvad, Sylvester; Lund, Philip M.; Munk, Chastine F.; Møller, Theis; Nehme, Ola M. Z.; Nejrup, Mathilde Rove; Nexø, Louise; Nielsen, Simon Skødt Holm; Niemeier, Nicolai; Nikolajsen, Lasse V.; Nøhr, Peter C. T.; Skaarup Ovesen, Jacob; Paustian, Lucas; Pedersen, Adam S.; Petersen, Mathias K.; Poulsen, Camilla M.; Praeger-Jahnsen, Louis; Qureshi, L. Sonia; Schiermacher, Louise S.; Simris, Martin B.; Smith, Gorm; Smith, Heidi N.; Sonne, Alexander K.; Zenulovic, Marko R.; Winther Sørensen, Alma; Vogt, Emil; Væring, Andreas; Westermann, Jonas; Özcan, Sevin B.

    2018-01-01

    Three series of ionic self-assembled materials based on anionic azo-dyes and cationic benzalkonium surfactants were synthesized and thin films were prepared by spin-casting. These thin films appear isotropic when investigated with polarized optical microscopy, although they are highly anisotropic. Here, three series of homologous materials were studied to rationalize this observation. Investigating thin films of ordered molecular materials relies to a large extent on advanced experimental methods and large research infrastructure. A statement that in particular is true for thin films with nanoscopic order, where X-ray reflectometry, X-ray and neutron scattering, electron microscopy and atom force microscopy (AFM) has to be used to elucidate film morphology and the underlying molecular structure. Here, the thin films were investigated using AFM, optical microscopy and polarized absorption spectroscopy. It was shown that by using numerical method for treating the polarized absorption spectroscopy data, the molecular structure can be elucidated. Further, it was shown that polarized optical spectroscopy is a general tool that allows determination of the molecular order in thin films. Finally, it was found that full control of thermal history and rigorous control of the ionic self-assembly conditions are required to reproducibly make these materials of high nanoscopic order. Similarly, the conditions for spin-casting are shown to be determining for the overall thin film morphology, while molecular order is maintained. PMID:29462883

  16. Synthesis, Spectral, Thermogravimetric, XRD, Molecular Modelling and Potential Antibacterial Studies of Dimeric Complexes with Bis Bidentate ON–NO Donor Azo Dye Ligands

    Directory of Open Access Journals (Sweden)

    Bipin Bihari Mahapatra

    2013-01-01

    Full Text Available The dimeric complexes of Co(II, Ni(II, Cu(II, Zn(II, Cd(II, and Hg(II with two new symmetrical ON–NO donor bis bidentate (tetradentate azo dye ligands, LH2 = 4,4′-bis(4′-hydroxyquinolinolinylazodiphenylsulphone, and L′H2 = 4,4′-bis(acetoacetanilideazodiphenylsulphone have been synthesized. The metal complexes have been characterised by elemental analytical, conductance, magnetic susceptibility, IR, electronic spectra, ESR, NMR, thermogravimetry, X-ray diffraction (powder pattern spectra, and molecular modelling studies. The Co(II and Ni(II complexes are found to be octahedral, Cu(II complexes are distorted octahedral, and a tetrahedral stereochemistry has been assigned to Zn(II, Cd(II, and Hg(II complexes. The thermogravimetric study indicates that compounds are quite stable. The energy optimized structures are proposed using the semiempirical ZINDO/1 quantum mechanical calculations. The potential antibacterial study of the ligands and some metal complexes has been made with one gram positive bacteria Staphylococcus aureus and one gram negative bacteria E. coli which gives encouraging results. Both the Co(II complexes are found to possess monoclinic crystal system.

  17. Using Polarized Spectroscopy to Investigate Order in Thin-Films of Ionic Self-Assembled Materials Based on Azo-Dyes

    Directory of Open Access Journals (Sweden)

    Miguel R. Carro-Temboury Martin Kühnel

    2018-02-01

    Full Text Available Three series of ionic self-assembled materials based on anionic azo-dyes and cationic benzalkonium surfactants were synthesized and thin films were prepared by spin-casting. These thin films appear isotropic when investigated with polarized optical microscopy, although they are highly anisotropic. Here, three series of homologous materials were studied to rationalize this observation. Investigating thin films of ordered molecular materials relies to a large extent on advanced experimental methods and large research infrastructure. A statement that in particular is true for thin films with nanoscopic order, where X-ray reflectometry, X-ray and neutron scattering, electron microscopy and atom force microscopy (AFM has to be used to elucidate film morphology and the underlying molecular structure. Here, the thin films were investigated using AFM, optical microscopy and polarized absorption spectroscopy. It was shown that by using numerical method for treating the polarized absorption spectroscopy data, the molecular structure can be elucidated. Further, it was shown that polarized optical spectroscopy is a general tool that allows determination of the molecular order in thin films. Finally, it was found that full control of thermal history and rigorous control of the ionic self-assembly conditions are required to reproducibly make these materials of high nanoscopic order. Similarly, the conditions for spin-casting are shown to be determining for the overall thin film morphology, while molecular order is maintained.

  18. Microwave-enhanced UV/H2O2 degradation of an azo dye (tartrazine): optimization, colour removal, mineralization and ecotoxicity.

    Science.gov (United States)

    Parolin, Fernanda; Nascimento, Ulisses Magalhães; Azevedo, Eduardo Bessa

    2013-01-01

    This study optimizes two factors, pH and initial [H2O2], in the ultraviolet (UV)/H2O2/microwave (MW) process through experimental design and assesses the effect of MWs on the colour removal of an azo-dye (tartrazine) solution that was favoured by an acidic pH. The estimated optimal conditions were: initial [H2O2] = 2.0 mmol L(-1) and pH = 2.6, at 30 +/- 2 degrees C. We obtained colour removals of approximately 92% in 24 min of irradiation (EDL, 244.2 W), following zero order kinetics: k = (3.9 +/- 0.52) x 10(-2) a.u. min(-1) and R2 = 0.989. Chemical and biological oxygen demand were significantly removed. On the other hand, the carbon content, biodegradability and ecotoxicity (Lactuca sativa) remained approximately the same. The UV/H2O2/MW process was shown to be eight times faster than other tested processes (MW, H2O2, H2O2/MW, and UV/MW).

  19. Effect of food azo dyes tartrazine and carmoisine on biochemical parameters related to renal, hepatic function and oxidative stress biomarkers in young male rats.

    Science.gov (United States)

    Amin, K A; Abdel Hameid, H; Abd Elsttar, A H

    2010-10-01

    Tartrazine and carmoisine are an organic azo dyes widely used in food products, drugs and cosmetics. The present study conducted to evaluate the toxic effect of these coloring food additives; on renal, hepatic function, lipid profile, blood glucose, body-weight gain and biomarkers of oxidative stress in tissue. Tartrazine and carmoisine were administered orally in two doses, one low and the other high dose for 30 days followed by serum and tissue sample collection for determination of ALT, AST, ALP, urea, creatinine, total protein, albumin, lipid profile, fasting blood glucose in serum and estimation of GSH, catalase, SOD and MDA in liver tissue in male albino rat. Our data showed a significant increase in ALT, AST, ALP, urea, creatinine total protein and albumin in serum of rats dosed with tartrazine and carmoisine compared to control rats and these significant change were more apparent in high doses than low, GSH, SOD and Catalase were decreased and MDA increased in tissue homogenate in rats consumed high tartrazine and both doses of carmoisine. We concluded that tartrazine and carmoisine affect adversely and alter biochemical markers in vital organs e.g. liver and kidney not only at higher doses but also at low doses. Copyright (c) 2010 Elsevier Ltd. All rights reserved.

  20. Using Polarized Spectroscopy to Investigate Order in Thin-Films of Ionic Self-Assembled Materials Based on Azo-Dyes.

    Science.gov (United States)

    Kühnel, Miguel R Carro-Temboury Martin; Ahmad, Mariam; Andersen, Frederik; Bech, Ári Brend; Bendixen, H Krestian L; Nawrocki, Patrick R; Bloch, Anders J; Bora, Ilkay; Bukhari, Tahreem A; Bærentsen, Nicolai V; Carstensen, Jens; Chima, Smeeah; Colberg, Helene; Dahm, Rasmus T; Daniels, Joshua A; Dinckan, Nermin; Idrissi, Mohamed El; Erlandsen, Ricci; Førster, Marc; Ghauri, Yasmin; Gold, Mikkel; Hansen, Andreas; Hansen, Kenn; Helmsøe-Zinck, Mathias; Henriksen, Mathias; Hoffmann, Sophus V; Hyllested, Louise O H; Jensen, Casper; Kallenbach, Amalie S; Kaur, Kirandip; Khan, Suheb R; Kjær, Emil T S; Kristiansen, Bjørn; Langvad, Sylvester; Lund, Philip M; Munk, Chastine F; Møller, Theis; Nehme, Ola M Z; Nejrup, Mathilde Rove; Nexø, Louise; Nielsen, Simon Skødt Holm; Niemeier, Nicolai; Nikolajsen, Lasse V; Nøhr, Peter C T; Orlowski, Dominik B; Overgaard, Marc; Ovesen, Jacob Skaarup; Paustian, Lucas; Pedersen, Adam S; Petersen, Mathias K; Poulsen, Camilla M; Praeger-Jahnsen, Louis; Qureshi, L Sonia; Ree, Nicolai; Schiermacher, Louise S; Simris, Martin B; Smith, Gorm; Smith, Heidi N; Sonne, Alexander K; Zenulovic, Marko R; Sørensen, Alma Winther; Sørensen, Karina; Vogt, Emil; Væring, Andreas; Westermann, Jonas; Özcan, Sevin B; Sørensen, Thomas Just

    2018-02-15

    Three series of ionic self-assembled materials based on anionic azo-dyes and cationic benzalkonium surfactants were synthesized and thin films were prepared by spin-casting. These thin films appear isotropic when investigated with polarized optical microscopy, although they are highly anisotropic. Here, three series of homologous materials were studied to rationalize this observation. Investigating thin films of ordered molecular materials relies to a large extent on advanced experimental methods and large research infrastructure. A statement that in particular is true for thin films with nanoscopic order, where X-ray reflectometry, X-ray and neutron scattering, electron microscopy and atom force microscopy (AFM) has to be used to elucidate film morphology and the underlying molecular structure. Here, the thin films were investigated using AFM, optical microscopy and polarized absorption spectroscopy. It was shown that by using numerical method for treating the polarized absorption spectroscopy data, the molecular structure can be elucidated. Further, it was shown that polarized optical spectroscopy is a general tool that allows determination of the molecular order in thin films. Finally, it was found that full control of thermal history and rigorous control of the ionic self-assembly conditions are required to reproducibly make these materials of high nanoscopic order. Similarly, the conditions for spin-casting are shown to be determining for the overall thin film morphology, while molecular order is maintained.

  1. New azo dyes as colored isoelectric point markers for isoelectric focusing in acidic pH region

    Czech Academy of Sciences Publication Activity Database

    Šťastná, Miroslava; Trávníček, Martin; Šlais, Karel

    2005-01-01

    Roč. 26, č. 1 (2005), s. 53-59 ISSN 0173-0835 R&D Projects: GA AV ČR(CZ) IBS4031201; GA ČR(CZ) GA203/02/1447; GA AV ČR IAA4031302 Keywords : ampholytic dyes * pI markers Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.850, year: 2005

  2. Effect of AZO on GO-NO-GO radiation indicator

    International Nuclear Information System (INIS)

    Hasan Sham; Taiman Kadni; Noriah Mod Ali

    2002-01-01

    The purpose of the study is to evaluate the effect of Azo group dyes as an radiation indicator. Dimethyl Yellow, Alizarin Red, Congo Red, Methyl Violet and Bromophenol Blue dyes were used to compare the capability of each dye to change colour in response to radiation. Sensitivity of single and incorporated dyes were identified by exposing them to 5-50 kGy gamma radiation. The result shows that the Azo group is more sensitive to radiation compare to other groups. (Author)

  3. Removal of binary azo dyes from water by UV-irradiated degradation in TiO2 suspensions

    International Nuclear Information System (INIS)

    Juang, Ruey-Shin; Lin, Su-Hsia; Hsueh, Pei-Ying

    2010-01-01

    Photodegradation and mineralization of single and binary Acid Orange 7 (AO7) and Reactive Red 2 (RR2) under UV irradiation in TiO 2 suspensions was examined. Experiments were conducted as a function of initial pH, TiO 2 dose, and initial dye concentration. First-order derivative spectrophotometric method was used to simultaneously analyze AO7 and RR2 in binary solutions. The Langmuir-Hinshelwood kinetic model was applied to evaluate and compare the apparent rate constants for the photodegradation of both dyes in single and binary solutions. It was shown that photodegradation of both dyes in binary solution was slower than those in single solution under comparable conditions. Moreover, the difference between the apparent rate constants of RR2 and AO7 became smaller in contrast to the cases of single solutions. After 20-min UV irradiation with 0.5 g/L TiO 2 , complete removal of single 0.086 mM AO7 and 0.086 mM RR2 at pH 6.8 was obtained, but only 60% and 45% of binary 0.086 mM AO7 and 0.086 mM RR2 was removed, respectively.

  4. Synthesis, structural characterization of nano ZnTiO3 ceramic: An effective azo dye adsorbent and antibacterial agent

    Directory of Open Access Journals (Sweden)

    R.S. Raveendra

    2014-12-01

    Full Text Available Nanocrystalline meta-zinc titanate (ZnTiO3 ceramic was prepared using a self-propagating solution combustion synthesis (SCS for the first time using urea as fuel. The product was calcined at 800 °C for 2 h to improve the crystallinity. Powder X-ray diffraction (PXRD, Fourier transform infrared spectroscopy (FTIR, scanning electron microscopy (SEM, energy-dispersive X-ray spectroscopy (EDAX, high resolution transmission electron microscopy (HR-TEM and UV–vis absorption spectroscopy were used to characterize the final product. PXRD results show that the ilmenite type rhombohedral structure was formed when the sample was calcined at 800 °C for 2 h. Adsorption experiments were performed with cationic malachite green (MG dye. ∼96% dye was adsorbed onto nanocrystalline ZnTiO3 ceramic at pH 9 for 30 min of the contact time. The optimum adsorbent dose was found to be 0.45 g/L of dye. Langmuir–Hinshelwood model was used to study adsorption kinetics and first order kinetic model best describes the MG adsorption on ZnTiO3. Antibacterial activity was investigated against gram negative Klebsiella aerogenes, Pseudomonas desmolyticum, Escherichia coli, and gram positive Staphylococcus aureus bacteria by agar well diffusion method. Nanocrystalline ZnTiO3 ceramic showed significant effect on all the four bacterial strains at the concentration of 1000 and 1500 μg per well.

  5. Assessment of toxicity and genotoxicity of the reactive azo dyes Remazol Black B and Remazol Orange 3R and effectiveness of electron beam irradiation in the reduction of color and toxic effects

    International Nuclear Information System (INIS)

    Pinheiro, Alessandro de Sa

    2011-01-01

    The textile industries play an important role in national and global economy. But, their activities are considered potentially polluting. The use of large volumes of water and the production of colored wastewater with high organic matter are among the main issues raised, especially during the stage of dyeing and washing of the textile process. The reactive azo dyes are the main colors used in the industry for dyeing of cotton in Brazil and worldwide. Because of its low setting and variations in the fiber production process, about 30% of the initial concentration used in the dyeing baths are lost and will compose the final effluent. These compounds have a low biodegradability, are highly soluble in water and therefore are not completely removed by conventional biological processes. In addition, other processes do not promote degradation but the transference to solid environment. The dyes discarded without treatment in the water body can cause aesthetic modifications, alter photosynthesis and gas solubility, as well as being toxic and genotoxic. The main objectives of this study were to evaluate the toxicity and genotoxicity of two reactive azo dyes (Remazol Black B - RPB and Remazol Orange 3R - R3AR) and the percentage of color and toxicity reduction after the use of electron beam radiation. The acute toxicity assays performed with Vibrio fischeri, Daphnia similis and Biomphalaria glabrata showed different response patterns for dyes. The different chemical forms of dyes were slightly toxic to Vibrio fischeri and only the RPB dye (vinylsulphone) was toxic (EC50 15min = 6,23 mg L-1). In tests with Daphnia similis, the dye RPB was slightly toxic in its pattern form, sulphatoethylsulphone, (CE50 48h = 91,25 mg L -1 ) and showed no toxicity in other chemical forms. However, the RA3R dye was toxic to the dafnids and the vinylsulphone form very toxic (EC50 48h = 0,54 mg L-1). No toxicity was observed in Biomphalaria glabrata assays. Chronic toxicity was assessed with the

  6. Thermal modification of activated carbon surface chemistry improves its capacity as redox mediator for azo dye reduction.

    Science.gov (United States)

    Pereira, L; Pereira, R; Pereira, M F R; van der Zee, F P; Cervantes, F J; Alves, M M

    2010-11-15

    The surface chemistry of a commercial AC (AC(0)) was selectively modified, without changing significantly its textural properties, by chemical oxidation with HNO(3) (AC(HNO3)) and O(2) (AC(O2)), and thermal treatments under H(2) (AC(H2)) or N(2) (AC(N2)) flow. The effect of modified AC on anaerobic chemical dye reduction was assayed with sulphide at different pH values 5, 7 and 9. Four dyes were tested: Acid Orange 7, Reactive Red 2, Mordant Yellow 10 and Direct Blue 71. Batch experiments with low amounts of AC (0.1 g L(-1)) demonstrated an increase of the first-order reduction rate constants, up to 9-fold, as compared with assays without AC. Optimum rates were obtained at pH 5 except for MY10, higher at pH 7. In general, rates increased with increasing the pH of point zero charge (pH(pzc)), following the trend AC(HNO3) granular biomass, AC(H2) also duplicated and increase 4.5-fold the decolourisation rates of MY10 and RR2, respectively. In this last experiment, reaction rate was independent of AC concentration in the tested range 0.1-0.6 g L(-1). Copyright © 2010 Elsevier B.V. All rights reserved.

  7. Modeling of Reactive Blue 19 azo dye removal from colored textile wastewater using L-arginine-functionalized Fe{sub 3}O{sub 4} nanoparticles: Optimization, reusability, kinetic and equilibrium studies

    Energy Technology Data Exchange (ETDEWEB)

    Dalvand, Arash; Nabizadeh, Ramin [Department of Environmental Health Engineering, School of Public Health, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Reza Ganjali, Mohammad [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of); Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Khoobi, Mehdi [Medical Biomaterials Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 14176 (Iran, Islamic Republic of); Nazmara, Shahrokh [Department of Environmental Health Engineering, School of Public Health, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Hossein Mahvi, Amir, E-mail: ahmahvi@yahoo.com [Department of Environmental Health Engineering, School of Public Health, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Center for Solid Waste Research, Institute for Environmental Research, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); National Institute of Health Research, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2016-04-15

    This study aimed to investigate the removal of Reactive Blue 19 from colored wastewater using Fe{sub 3}O{sub 4} magnetic nanoparticles modified with L-arginine (Fe{sub 3}O{sub 4}@L-arginine). In order to investigate the effect of independent variables on dye removal and determining the optimum condition, the Box–Behnken Design (BBD) under Response Surface Methodology (RSM) was employed. Fe{sub 3}O{sub 4}@L-arginine nanoparticles were synthesized and characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and vibrating sample magnetometer. Applying Fe{sub 3}O{sub 4}@L-arginine nanoparticles for dye removal showed that; by increasing adsorbent dose and decreasing pH, dye concentration, and ionic strength dye removal has been increased. In the optimum condition, Fe{sub 3}O{sub 4}@L-arginine nanoparticles were able to remove dye as high as 96.34% at an initial dye concentration of 50 mg/L, adsorbent dose of 0.74 g/L, and pH 3. The findings indicated that dye removal followed pseudo-second-order kinetic (R{sup 2}=0.999) and Freundlich isotherm (R{sup 2}=0.989). Based on the obtained results, as an efficient and reusable adsorbent, Fe{sub 3}O{sub 4}@L-arginine nanoparticles can be successfully applied for dye removal from colored wastewater. - Highlights: • The Fe{sub 3}O{sub 4}@L-arginine removed RB 19 azo dye from wastewater efficiently. • BBD under RSM was used to analyze and optimize the adsorption process. • pH was the most influential parameter in dye removal.

  8. Biofilm inhibition formation of clinical strains of Pseudomonas aeruginosa mutans, photocatalytic activity of azo dye and GC-MS analysis of leaves of Lagerstroemia speciosa.

    Science.gov (United States)

    Sai Saraswathi, V; Kamarudheen, Neethu; Bhaskara Rao, K V; Santhakumar, K

    2017-04-01

    The investigation was conducted to analyse the bioactive compounds from the leaf extracts of L. speciosa by GC-MS. The extracts were screened for antibacterial and antibiofilm activities against potential clinical strains. The bioactive compounds from the leaves of L. speciosa were extracted by soxhlet continuous extraction method and their chemical composition was analysed by Gas Chromatography-Mass Spectroscopy (GC-MS). The antibacterial activity was evaluated against clinical strain like Staphylococcus aureus, Escherichia coli, P. aeruginosa and Salmonella typhi by well diffusion technique. We also screened for antibacterial property against common food borne pathogens namely Listeria monocytogenes and Bacillus cereus at varied concentration 250μml -1 to 1000μml -1 . Thereafter antibiofilm assay was carried out at from 250 to 1000μg/ml against P. aeruginosa (high biofilm forming pathogen) clinical strain by cover slip technique and the morphology of the pathogen was observed using Scanning Electron Microscopy-(SEM). It was observed that diverse class of secondary metabolites were found by GC-MS analysis for all the extracts upon the continuous extraction. It was found that only minimum inhibition was seen in alcoholic extract for antibacterial activity, whereas all other extracts showed negligible activity. P. aeruginosa biofilm inhibited to 93.0±2% and 91±2% at higher concentration (1000μg/ml) for methanolic and ethanolic extract respectively. Absence of extracellular matrix structure and the surface cracking of biofilm were viewed by SEM, which confirmed the antibiofilm activity. Hence this study reveals that L. speciosa showed significant antibiofilm activity against P. aeruginosa due to the phytoconstituents present in the leaf extracts which was well documented in the alcoholic extracts by GC-MS analysis. The methanolic and ethanolic extract showed good photocatalytic activity of 77.44% and 96.66% against azo dye degradation respectively. Further

  9. Influence of generated intermediates’ interaction on heterogeneous Fenton's degradation of an azo dye 1-diazo-2-naphthol-4-sulfonic acid by using sludge based carbon as catalyst

    International Nuclear Information System (INIS)

    Gu, Lin; Huang, Shouqiang; Zhu, Nanwen; Zhang, Daofang; Yuan, Haiping; Lou, Ziyang

    2013-01-01

    Highlights: • End-products have higher tendency to be adsorbed on SC than primarily-formed. • Higher initial H 2 O 2 dosage results in intermediates with strong polarity. • 9 model intermediates differ in their behavior on interactions with catalysts. • Polar surface area dominated their adsorption on SC while K ow acts as a key role on HSC. -- Abstract: Sewage sludge based carbons have recently been used as novel catalyst in heterogeneous Fenton's reactions to degrade azo dye molecules. The carbons, functioning as both catalyst and adsorbent, play an important role in pollutants elimination, especially for those simultaneously generated organic intermediates. Different factors, i.e., H 2 O 2 concentration, may influence the type and properties of those intermediates and may have great impacts on their elimination through the interactions with catalysts’ surface. Thus, techniques including Temperature Programmed Desorption-Mass Spectrometer (TPD-MS), N 2 adsorption isotherm and Scanning Electron Microscope (SEM) were used to probe the ways of the interaction between oxidation products and catalyst by using different initial H 2 O 2 concentrations (10 and 20 mM). The higher Chemical Oxygen Demand (COD) removal with 20 mM H 2 O 2 was found to be related not only to the higher hydroxyl radicals but also the specific interactions between the intermediates and catalyst’ surface. The deep oxidation occurred in the conditions with higher oxidant amount enhances the intermediates’ adsorption on catalyst, thus increasing the COD removal by large margin. Simulated adsorption experiments by using six primarily formed intermediates and three deeply mineralized products on three different catalysts also confirmed the assumption. Results suggested close relations between adsorption capacities and intermediates’ properties such as polar surface area and octanol-water partition coefficient

  10. Dichroic dye-dependent studies in guest-host polymer-dispersed liquid crystal films

    Energy Technology Data Exchange (ETDEWEB)

    Malik, Praveen, E-mail: pmalik100@yahoo.co [Department of Physics, Dr. B.R. Ambedkar National Institute of Technology, Jalandhar 144011, Punjab (India); Raina, K.K. [Liquid Crystal Group, Materials Research Laboratory, School of Physics and Materials Science, Thapar University, Patiala 147004, Punjab (India)

    2010-01-01

    Guest-host polymer-dispersed liquid crystal (GHPDLC) films were prepared using a nematic liquid crystal, photo-curable polymer and dichroic dye (anthraquinone blue) by polymerization-induced phase separation (PIPS) technique. Non-ionic dichroic dye (1%, 2% and 4% wt./wt. ratio) was taken as guest in PDLC host. Polarizing microscopy shows that in the absence of electric field, liquid crystal (LC) droplets in polymer matrix mainly exhibit bipolar configuration, however, relatively at higher field, maltese-type crosses were observed. Our results show that approx1% dye-doped PDLC film shows better transmission and faster response times over pure polymer-dispersed nematic liquid crystal (PDNLC) and higher concentrated (2% and 4%) GHPDLC films.

  11. Dichroic dye-dependent studies in guest-host polymer-dispersed liquid crystal films

    International Nuclear Information System (INIS)

    Malik, Praveen; Raina, K.K.

    2010-01-01

    Guest-host polymer-dispersed liquid crystal (GHPDLC) films were prepared using a nematic liquid crystal, photo-curable polymer and dichroic dye (anthraquinone blue) by polymerization-induced phase separation (PIPS) technique. Non-ionic dichroic dye (1%, 2% and 4% wt./wt. ratio) was taken as guest in PDLC host. Polarizing microscopy shows that in the absence of electric field, liquid crystal (LC) droplets in polymer matrix mainly exhibit bipolar configuration, however, relatively at higher field, maltese-type crosses were observed. Our results show that ∼1% dye-doped PDLC film shows better transmission and faster response times over pure polymer-dispersed nematic liquid crystal (PDNLC) and higher concentrated (2% and 4%) GHPDLC films.

  12. CaSnO 3 obtained by modified Pechini method applied in the photocatalytic degradation of an azo dye

    Directory of Open Access Journals (Sweden)

    G. L. Lucena

    Full Text Available Abstract Pure forms of alkaline-earth stannates with perovskite structure (ASnO3, A= Ca2+, Sr2+, Ba2+ have been used as photocatalysts. In this work, CaSnO3 perovskite sample was synthesized by a modified Pechini method at 800 ºC and characterized by X-ray diffraction (XRD, UV-visible spectroscopy, infrared spectroscopy and Raman spectroscopy. The photocatalytic degradation of remazol golden yellow (RNL dye under UV radiation was evaluated. The XRD pattern showed that the synthesis method favored the orthorhombic CaSnO3 crystallization. According to the Raman spectrum, a material with high short-range order was obtained despite of the relatively low synthesis temperature, compared to the solid-state reaction one. The highest photocatalytic activity was attained at pH 3, which presented 51% discoloration and improved activity of 35% compared to discoloration solely due to adsorption (absence of radiation. The point of zero charge (PZC and the photocatalytic results indicated that a direct mechanism prevailed at pH 3, whereas an indirect mechanism prevailed at pH 6.

  13. Ultrasonically facilitated adsorption of an azo dye onto nanostructures obtained from cellulosic wastes of broom and cooler straw.

    Science.gov (United States)

    Safari, Mahdi; Khataee, Alireza; Darvishi Cheshmeh Soltani, Reza; Rezaee, Reza

    2018-07-15

    In the present work, ultrasonically facilitated adsorption (UFA) of a cationic dye [Basic Red 46 (BR46)] was examined using cellulosic nanostructures obtained from broom and cooler straw. Although the exclusive application of the nanostructured broom resulted in the 43.51% adsorption of BR46, the UFA process gave rise to the substantial removal efficiency of about 93%. In the case of the nanostructured straw, the efficiency was increased from 36.9% to 55.7%. The UFA process for both adsorbents reached the equilibrium within 60 min which was shorter than the time for the only adsorption. According to the values of the mean free energy (E), the decolorization via the UFA process applying broom (15.81 kJ/mol) and straw (11.18 kJ/mol) nanostructures was occurred chemically. An insignificant loss in the adsorption capacity of both adsorbents was observed after three regeneration tests by means of 0.05 M hydrochloric acid, indicating the good reusability potential of the as-synthesized cellulosic nanostructures. Copyright © 2018 Elsevier Inc. All rights reserved.

  14. Optimization for decolorization of azo dye acid green 20 by ultrasound and H2O2 using response surface methodology

    International Nuclear Information System (INIS)

    Zhang Zhanmei; Zheng Huaili

    2009-01-01

    Response surface methodology (RSM) based on Box-Behnken design was successfully applied to the optimization of the operating conditions in decolorization of acid green 20 (AG 20) by ultrasonic irradiation in the presence of H 2 O 2 . The effects of three operating variables, ultrasonic power density, initial pH value of dye solution and H 2 O 2 concentration on the decolorization efficiency of AG 20 were evaluated. A quadratic model for AG 20 decolorization was proposed. Analysis of variance (ANOVA) indicated that the proposed quadratic model could be used to navigate the design space. The proposed model was approximately in accordance with the experimental case with correlation coefficients R 2 and R adj 2 of 0.9995 and 0.9984, respectively. The optimum operating conditions for AG 20 decolorization were found to be 1.08 W/mL of ultrasonic power density, 4.85 of initial pH and 1.94 mM of H 2 O 2 concentration, respectively. The predicted decolorization rate under the optimum conditions determined by RSM was 96.8%. Confirmatory tests were carried out under the optimum conditions and the decolorization rate of 96.3% was observed, which closely agreed with the predicted value. The results confirmed that RSM based on Box-Behnken design was an accurate and reliable method to optimize the operating conditions of AG 20 decolorization.

  15. Facile Preparation of Phosphotungstic Acid-Impregnated Yeast Hybrid Microspheres and Their Photocatalytic Performance for Decolorization of Azo Dye

    Directory of Open Access Journals (Sweden)

    Lan Chen

    2013-01-01

    Full Text Available Phosphotungstic acid (HPW-impregnated yeast hybrid microspheres were prepared by impregnation-adsorption technique through tuning pH of the aqueous yeast suspensions. The obtained products were characterized by field emission scanning electron microscopy (FE-SEM, energy dispersive spectrometry (EDS, X-ray diffraction (XRD, thermogravimetry-differential scanning calorimetry (TG-DSC, and ultraviolet-visible spectrophotometry (UV-Vis, respectively. FE-SEM and EDS ascertain that the HPW has been effectively introduced onto the surface of yeast, and the resulting samples retain ellipsoid shape, with the uniform size (length 4.5 ± 0.2 μm, width 3.0 ± 0.3 μm and good monodispersion. XRD pattern indicates that the main crystal structure of as-synthesized HPW@yeast microsphere is Keggin structure. TG-DTA states that the HPW in composites has better thermal stability than pure HPW. Fourier transform infrared spectroscopy (FT-IR elucidates that the functional groups or chemical bonds inherited from the pristine yeast cell were critical to the assembling of the composites. UV-Vis shows that the obtained samples have a good responding to UV light. The settling ability indicates that the hybrid microspheres possess an excellent suspension performance. In the test of catalytic activity, the HPW@yeast microsphere exhibits a high photocatalytic activity for the decoloration of Methylene blue and Congo red dye aqueous solutions, and there are a few activity losses after four cycles of uses.

  16. Cancer risk assessment of azo dyes and aromatic amines from tattoo bands, folders of paper, toys, bed clothes, watch straps and ink

    NARCIS (Netherlands)

    Zeilmaker MJ; van Kranen HJ; van Veen MP; Janus J; LBM

    2000-01-01

    Dit rapport beschrijft een schatting voor het risico op kanker dat verbonden is aan het gebruik van tatoe bandjes, kinderspeelpapier, speelgoed, beddengoed, lederen horlogebandjes en inkt waarin kankerverwekkende azo kleurstoffen aangetroffen zijn. In genoemde producten zijn benzidine en de

  17. Rapid degradation of azo dye Direct Black BN by magnetic MgFe{sub 2}O{sub 4}-SiC under microwave radiation

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Jia; Yang, Shaogui, E-mail: yangsg@nju.edu.cn; Li, Na; Meng, Lingjun; Wang, Fei; He, Huan; Sun, Cheng

    2016-08-30

    Highlights: • MgFe{sub 2}O{sub 4}-SiC was first successfully synthesized. • MgFe{sub 2}O{sub 4}-SiC attained the maximum absorbing value of 13.32 dB at 2.57 GHz, which reached extremely high RL value at low frequency range. • Fast decolorization and high TOC removal of azo dye Direct Black BN with complicated structure could occur with MgFe{sub 2}O{sub 4}-SiC under MW radiation. • MgFe{sub 2}O{sub 4}-SiC had better MW absorbing property and higher MW catalytic activity than MnFe{sub 2}O{sub 4}-SiC under the same condition. • MgFe{sub 2}O{sub 4}-SiC was of practical use in the wastewater treatment. - Abstract: A novel microwave (MW) catalyst, MgFe{sub 2}O{sub 4} loaded on SiC (MgFe{sub 2}O{sub 4}-SiC), was successfully synthesized by sol-gel method, and pure MgFe{sub 2}O{sub 4} was used as reference. The MgFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4}-SiC catalysts were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), N{sub 2} adsorption analyzer (BET specific surface area), X-ray photoelectron spectroscopy (XPS). The electromagnetic parameters of the prepared catalysts were measured by vector network analyzer. The reflection loss (RL) based on the electromagnetic parameters calculated in Matlab showed MgFe{sub 2}O{sub 4}-SiC attained the maximum absorbing value of 13.32 dB at 2.57 GHz, which reached extremely high RL value at low frequency range, revealing the excellent MW absorption property of MgFe{sub 2}O{sub 4}-SiC. MW-induced degradation of Direct Black BN (DB BN) over as-synthesized MgFe{sub 2}O{sub 4}-SiC indicated that degradation efficiency of DB BN (20 mg L{sup −1}) in 5 min reached 96.5%, the corresponding TOC removal was 65%, and the toxicity of DB BN after degradation by MgFe{sub 2}O{sub 4}-SiC obviously decreased. The good stability and applicability of MgFe{sub 2}O{sub 4}-SiC on the degradation process were also discovered. Moreover, the ionic chromatogram during degradation

  18. Improved power conversion efficiency of dye-sensitized solar cells using side chain liquid crystal polymer embedded in polymer electrolytes

    International Nuclear Information System (INIS)

    Cho, Woosum; Lee, Jae Wook; Gal, Yeong-Soon; Kim, Mi-Ra; Jin, Sung Ho

    2014-01-01

    Side chain liquid crystal polymer (SCLCP) embedded in poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-co-HFP)-based polymer electrolytes (PVdF-co-HFP:side chain liquid crystal polymer (SCLCP)) was prepared for dye-sensitized solar cell (DSSC) application. The polymer electrolytes contained tetrabutylammonium iodide (TBAI), iodine (I 2 ), and 8 wt% PVdF-co-HFP in acetonitrile. DSSCs comprised of PVdF-co-HFP:SCLCP-based polymer electrolytes displayed enhanced redox couple reduction and reduced charge recombination in comparison to those of the conventional PVdF-co-HFP-based polymer electrolyte. The significantly increased short-circuit current density (J sc , 10.75 mA cm −2 ) of the DSSCs with PVdF-co-HFP:SCLCP-based polymer electrolytes afforded a high power conversion efficiency (PCE) of 5.32% and a fill factor (FF) of 0.64 under standard light intensity of 100 mW cm −2 irradiation of AM 1.5 sunlight. - Highlights: • We developed the liquid crystal polymer embedded on polymer electrolyte for DSSCs. • We fabricated the highly efficient DSSCs using polymer electrolyte. • The best PCE achieved for P1 is 5.32% using polymer electrolyte

  19. Improved power conversion efficiency of dye-sensitized solar cells using side chain liquid crystal polymer embedded in polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Woosum [Department of Chemistry Education, and Department of Frontier Materials Chemistry, and Institute for Plastic Information and Energy Materials, Pusan National University, Busan 609-735 (Korea, Republic of); Lee, Jae Wook, E-mail: jlee@donga.ac.kr [Department of Chemistry, Dong-A University, Busan 604-714 (Korea, Republic of); Gal, Yeong-Soon [Polymer Chemistry Lab, College of General Education, Kyungil University, Hayang 712-701 (Korea, Republic of); Kim, Mi-Ra, E-mail: mrkim2@pusan.ac.kr [Department of Polymer Science and Engineering, Pusan National University, Busan 609-735 (Korea, Republic of); Jin, Sung Ho, E-mail: shjin@pusan.ac.kr [Department of Chemistry Education, and Department of Frontier Materials Chemistry, and Institute for Plastic Information and Energy Materials, Pusan National University, Busan 609-735 (Korea, Republic of)

    2014-02-14

    Side chain liquid crystal polymer (SCLCP) embedded in poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-co-HFP)-based polymer electrolytes (PVdF-co-HFP:side chain liquid crystal polymer (SCLCP)) was prepared for dye-sensitized solar cell (DSSC) application. The polymer electrolytes contained tetrabutylammonium iodide (TBAI), iodine (I{sub 2}), and 8 wt% PVdF-co-HFP in acetonitrile. DSSCs comprised of PVdF-co-HFP:SCLCP-based polymer electrolytes displayed enhanced redox couple reduction and reduced charge recombination in comparison to those of the conventional PVdF-co-HFP-based polymer electrolyte. The significantly increased short-circuit current density (J{sub sc}, 10.75 mA cm{sup −2}) of the DSSCs with PVdF-co-HFP:SCLCP-based polymer electrolytes afforded a high power conversion efficiency (PCE) of 5.32% and a fill factor (FF) of 0.64 under standard light intensity of 100 mW cm{sup −2} irradiation of AM 1.5 sunlight. - Highlights: • We developed the liquid crystal polymer embedded on polymer electrolyte for DSSCs. • We fabricated the highly efficient DSSCs using polymer electrolyte. • The best PCE achieved for P1 is 5.32% using polymer electrolyte.

  20. Evaluation of the adsorbent properties of a zeolite rock modified for the removal of the azo dyes as water pollutants; Evaluacion de las propiedades adsorbentes de una roca zeolitica modificada para la remocion de colorantes azoicos como contaminantes del agua

    Energy Technology Data Exchange (ETDEWEB)

    Torres P, J

    2005-07-01

    At the moment some investigations which make reference to the removal of dyes for diverse adsorbent materials; as well as the factors that influence in the sorption process, considering the type so much of dye as those characteristics of the adsorbent material. In this work were investigated those adsorbent properties of a zeolite rock coming from San Luis Potosi State for the removal of azo dyes, using as peculiar cases the Red 40 (Red Allura) and the Yellow 5 (Tartrazine); for it were determined kinetic parameters and the sorption isotherms, as well as the sorption mechanisms involved in each case, between the dyes and the zeolite rock. In this work also it was considered the characterization before and after to removal of color from the water, through advanced analytical techniques such as the scanning electron microscopy of high vacuum (SEM), elementary microanalysis (EDS) and X-ray diffraction (XRD). The experimental part of the work fundamentally consisted, in the conditioning with a NaCl solution and later on the modification with HDTMA-Br of the natural zeolite rock, for then to put it in contact with solutions of the dyes R-40 and A-5, varying so much the contact times as the concentrations; the quantification of sodium in the liquid phase after the modification of the zeolite rock to determine the capacity of external cation exchange (CICE) it was carried out by means of the atomic absorption spectroscopy technique (EAA), and the quantification of the surfactant and the dyes in the liquid phase, it was carried out by means of the UV-vis spectrophotometry technique. It was found that the kinetic model that better it describes the process of sorption of R-40 and A-5 for the modified zeolite rock with HDTMA-Br, leaving of monocomponent and bi component solutions, it is the pseudo- second order. Inside of the obtained results for the sorption isotherms, as much the dye R-40 as the dye A-5 its presented a better adjustment to the Langmuir model. In what refers

  1. Enhanced transduction of photonic crystal dye lasers for gas sensing via swelling polymer film

    DEFF Research Database (Denmark)

    Smith, Cameron; Lind, Johan Ulrik; Christiansen, Mads Brøkner

    2011-01-01

    We present the enhanced transduction of a photonic crystal dye laser for gas sensing via deposition of an additional swelling polymer film. Device operation involves swelling of the polymer film during exposure to specific gases, leading to a change in total effective refractive index. Experimental...... in its application to other intracavity-based detection schemes to enable gas sensing. © 2011 Optical Society of America....

  2. Multimode laser emission from dye-doped hollow polymer optical fibre

    Indian Academy of Sciences (India)

    2014-02-09

    Feb 9, 2014 ... Dye-doped polymer optical fibre preforms were fabricated by the controlled polymeriza- tion of Rh B-doped methyl methacrylate (MMA). Hole in the preform can be achieved by placing a teflon rod on the centre of the glass tube during the polymerization. Final fibre structure with required diameter was ...

  3. Polymer photonic crystal dye lasers as label free evanescent cell sensors

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Lopacinska, Joanna M.; Jakobsen, Mogens Havsteen

    2009-01-01

    . The lasers are fabricated by combined nanoimprint and photolithography (CNP) in Ormocore hybrid polymer doped with the laser dye Pyrromethene 597. The lasers emit in the chip plane at a wavelength around 595 nm when pumped with 5 ns pulses from a compact frequency doubled Nd:YAG laser. We investigate...

  4. Micro-fabricated solid state dye lasers based on a photo-definable polymer

    DEFF Research Database (Denmark)

    Nilsson, Daniel; Balslev, Søren; Gregersen, Misha Marie

    2005-01-01

    the commercially available laser dye Rhodamine 6G, which is incorporated into the SU-8 polymer matrix. The single-mode slab waveguide is formed by three-step spin-coating deposition: a buffer layer of undoped SU-8, a core layer of SU-8 doped with Rhodamine, and a cladding layer of undoped SU-8. (c) 2005 Optical...

  5. Preparation of nanospinels NiMn{sub x}Fe{sub 2-x}O{sub 4} using sol-gel method and their applications on removal of azo dye from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Khosravi, Iman [Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad 917791436 (Iran, Islamic Republic of); Yazdanbakhsh, Mohammad, E-mail: myazdan@um.ac.ir [Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad 917791436 (Iran, Islamic Republic of); Goharshadi, Elaheh K. [Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad 917791436 (Iran, Islamic Republic of); Center of Nano Research, Ferdowsi University of Mashhad, Mashhad 91799 (Iran, Islamic Republic of); Youssefi, Abbas [Par -e- Tavous Research Institute, Mashhad 91000 (Iran, Islamic Republic of)

    2011-11-01

    Highlights: {yields} The nanospinels, NiMn{sub x}Fe{sub 2-x}O{sub 4} (x = 0.05, 0.1, 0.3, 0.5, 0.7, and 1), prepared by Sol-gel method. {yields} The nanospinels prepared, have been used for removal of approximately 90% of reactive blue 5 within 1 min. {yields} The degradation of RB5 dye, follows merely an adsorption process. - Abstract: In this paper, nanospinels NiMn{sub x}Fe{sub 2-x}O{sub 4} (x = 0.05, 0.1, 0.3, 0.5, 0.7, and 1) were prepared by sol-gel method in the presence of nitrate-metal-ethylene glycol (EG) polymerized complex. The nanospinels were characterized using thermogravimetry analysis (TGA), X-ray powder diffraction (XRD), Fourier infrared spectroscopy (FTIR), and transmission electron microscope (TEM). The adsorption of an azo dye, reactive blue 5 (RB5), from water was determined using the prepared nanospinels. The effect of operational parameters such as the initial dye concentration, the concentration of nanospinels, temperature, and pH on the degradation of dye was investigated. The adsorption process follows second-order kinetics and Arrhenius behavior. Two common models, the Langmuir and Freundlich isotherms were used to investigate the interaction of dye and nanospinels. The isotherm evaluations revealed that the Freundlich model provides better fit to the experimental data than that of the Langmuir model. The photocatalytic degradation of RB5 at pH 1 under UV irradiation was examined. The results showed that the degradation of RB5 dye follows merely an adsorption process.

  6. Thermal Dynamics of Xanthene Dye in Polymer Matrix Excited by Double Pulse Laser Radiation

    Science.gov (United States)

    Samusev, Ilia; Borkunov, Rodion; Tsarkov, Maksim; Konstantinova, Elizaveta; Antipov, Yury; Demin, Maksim; Bryukhanov, Valery

    2018-01-01

    Double-pulse laser excitation of the eosin and silver nanoparticles embedded into polymer media is known to be a method of electronic-vibrational energy deactivation kinetic process information obtaining and polymer thermal dynamics investigation. We have studied the vibrational relaxation processes in dye molecules (eosin) and nanoparticles in polyvinyl alcohol after two time-shifted laser pulses with fast and delayed fluorescence kinetics study. In order to simulate thermal and photophysical processes caused by double photon excitation, we solved heat transfer and energy deactivation differential equations numerically. The simulation allowed us to obtain the value of heat conductivity coefficient of polymer matrix.

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

    Energy Technology Data Exchange (ETDEWEB)

    Abbasi, Alireza, E-mail: aabbasi@khayam.ut.ac.ir [School of Chemistry, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Gharib, Maniya; Najafi, Mahnaz [School of Chemistry, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Janczak, Jan [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, PO Box 1410, 50-950 Wrocław (Poland)

    2016-03-15

    A new one-dimensional (1D) coordination polymer, [Zn(4,4′-bpy)(H{sub 2}O){sub 4}](ADC)·4H{sub 2}O (1) (4,4′-bpy=4,4′-bipyridine and H{sub 2}ADC=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. - Graphical abstract: A new 1D coordination polymer as catalyst for the degradation of Bismarck brown aqueous solution. - Highlights: • A 1D coordination polymer has been synthesized at room temperature. • The prepared compound was utilized for color removal of Bismarck brown dye. • Good catalytic activity and stability in the dye decolorization has been found.

  8. Solid State Polymer Electrolytes for Dye-sensitized Solar Cell

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    1 Introduction Over the past decade,Dye-sensitized solar cells (DSSCs) have been intensively investigated as potential alternatives to conventional inorganic photovoltaic devices due to their low production cost and high energy conversion[1-4]. This type of solar cell has achieved an impressive energy conversion efficiency of over 10%,whose electrolyte is a voltaic organic liquid solvent containing iodide/triiodide as redox couple.However,the use of a liquid electrolyte brings difficulties in the practi...

  9. [Adsorption and desorption of dyes by waste-polymer-derived activated carbons].

    Science.gov (United States)

    Lian, Fei; Liu, Chang; Li, Guo-Guang; Liu, Yi-Fu; Li, Yong; Zhu, Ling-Yan

    2012-01-01

    Mesoporous activated carbons with high surface area were prepared from three waste polymers, i. e., tire rubber, polyvinyl chloride (PVC) and polyethyleneterephtalate (PET), by KOH activation. The adsorption/desorption characteristics of dyes (methylene blue and methyl orange) on the carbons were studied. The effects of pH, ionic strength and surface surfactants in the solution on the dye adsorption were also investigated. The results indicated that the carbons derived from PVC and PET exhibited high surface area of 2 666 and 2 831 m2 x g(-1). Their mesopore volume were as high as 1.06 and 1.30 cm3 g(-1), respectively. 98.5% and 97.0% of methylene blue and methyl orange were removed in 15 min by PVC carbon, and that of 99.5% and 95.0% for PET carbon. The Langmuir maximum adsorption capacity to these dyes was more than 2 mmol x g(-1), much higher than that of commercial activated carbon F400. Compared with Freundlich model, the adsorption data was fitted better by Langmiur model, indicating monolayer coverage on the carbons. The adsorption was highly dependent on solution pH, ionic strength and concentration of surface surfactants. The activated carbons exhibited higher adsorption to methylene blue than that of methyl orange, and it was very hard for both of the dyes to be desorbed. The observation in this study demonstrated that activated carbons derived from polymer waste could be effective adsorbents for the treatment of wastewater with dyes.

  10. Influence of ionic strength in the adsorption and during photocatalysis of reactive black 5 azo dye on TiO{sub 2} coated on non woven paper with SiO{sub 2} as a binder

    Energy Technology Data Exchange (ETDEWEB)

    Aguedach, Abdelkahhar [Laboratoire de l' Eau et environnement, Universite Chouaib Doukkali, Faculte des Sciences, BP.20, El Jadida, Maroc (Morocco); Brosillon, Stephan [Laboratoire Science Chimiques de Rennes UMR 6226, Equipe Chimie et Ingenierie des Procedes, Ecole Nationale Superieure de Chimie, Universite Rennes 1, avenue du General Leclerc, 35700 Rennes (France)], E-mail: Stephan.Brosillon@ensc-rennes.fr; Morvan, Jean [Laboratoire Science Chimiques de Rennes UMR 6226, Equipe Chimie et Ingenierie des Procedes, Ecole Nationale Superieure de Chimie, Universite Rennes 1, avenue du General Leclerc, 35700 Rennes (France); Lhadi, El Kbir [Laboratoire de l' Eau et environnement, Universite Chouaib Doukkali, Faculte des Sciences, BP.20, El Jadida, Maroc (Morocco)

    2008-01-31

    Reactive black 5 (RB5), an azo dye, was degraded by using UV-irradiated TiO{sub 2} coated on non woven paper with SiO{sub 2} as a binder. The adsorption capacity of the photocatalyst was studied at natural pH, superior to pH{sub pzc} of the binder, for various ionic strengths. Different salts such as NaCl, KCl, CaCl{sub 2}, LiCl, Ca(NO{sub 3}){sub 2} were used to increase the ionic strength. The presence of salt increased the adsorption capacity. The electrostatic interactions between dye and oxide surface charges (TiO{sub 2}/SiO{sub 2}) is very important in the adsorption phenomena. The effect of the ionic strength of the solution on photocatalyst degradation was studied. The rate of degradation was increased by the presence of salts in the range of the experimental conditions. The increase of the initial decolorization rate was observed in the following order: Ca{sup 2+} > K{sup +} > Na{sup +} > Li{sup +}. Experiments with different anions (Cl{sup -}, NO{sub 3}{sup -}) had shown that nitrate was an indifferent electrolyte for the adsorption and photodegradation of the dye on SiO{sub 2}/TiO{sub 2}.

  11. Influence of ionic strength in the adsorption and during photocatalysis of reactive black 5 azo dye on TiO2 coated on non woven paper with SiO2 as a binder

    International Nuclear Information System (INIS)

    Aguedach, Abdelkahhar; Brosillon, Stephan; Morvan, Jean; Lhadi, El Kbir

    2008-01-01

    Reactive black 5 (RB5), an azo dye, was degraded by using UV-irradiated TiO 2 coated on non woven paper with SiO 2 as a binder. The adsorption capacity of the photocatalyst was studied at natural pH, superior to pH pzc of the binder, for various ionic strengths. Different salts such as NaCl, KCl, CaCl 2 , LiCl, Ca(NO 3 ) 2 were used to increase the ionic strength. The presence of salt increased the adsorption capacity. The electrostatic interactions between dye and oxide surface charges (TiO 2 /SiO 2 ) is very important in the adsorption phenomena. The effect of the ionic strength of the solution on photocatalyst degradation was studied. The rate of degradation was increased by the presence of salts in the range of the experimental conditions. The increase of the initial decolorization rate was observed in the following order: Ca 2+ > K + > Na + > Li + . Experiments with different anions (Cl - , NO 3 - ) had shown that nitrate was an indifferent electrolyte for the adsorption and photodegradation of the dye on SiO 2 /TiO 2

  12. Conducting polymers based counter electrodes for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Veerender, P., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Saxena, Vibha, E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Gusain, Abhay, E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Jha, P., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Koiry, S. P., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Chauhan, A. K., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Aswal, D. K., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com; Gupta, S. K., E-mail: veeru1009@gmail.com, E-mail: veeru1009@gmail.com [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai - 400085 (India)

    2014-04-24

    Conducting polymer films were synthesized and employed as an alternative to expensive platinum counter electrodes for dye-sensitized solar cells. poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) thin films were spin-coated and polypyrrole films were electrochemically deposited via cyclic voltammetry method on ITO substrates. The morphology of the films were imaged by SEM and AFM. These films show good catalytic activity towards triiodide reduction as compared to Pt/FTO electrodes. Finally the photovoltaic performance of DSSC fabricated using N3 dye were compared with PT/FTO, PEDOT/ITO, and e-PPy counter electrodes.

  13. Novelionic Polymer Electrolytes for Dye Sensitized Solar Cell

    Institute of Scientific and Technical Information of China (English)

    Li Wang; Shibi Fang; Yuan Lin

    2005-01-01

    @@ 1Introduction In recent years, dye-sensitized solar cells(DSC) based on nanocrystalline porous TiO2 films have attracted much attention because of their relatively higher efficiency and low cost compared with conventional inorganic photovoltaic devices[1]. This type of solar cell has achieved an impressive photo-to-energy conversion efficiency of over 10% where the electrolyte is volatile organic liquid solvents containing I-/I-3- as redox couple. Because of high volatilities, solvent losses occur during long-term operations, resulting in lowered DSC performances.And leakage of liquid electrolyte also limits the durability of DSC.

  14. Single-mode solid-state polymer dye laser fabricated with standard I-line UV lithography

    DEFF Research Database (Denmark)

    Balslev, Søren; Mironov, Andrej; Nilsson, Daniel

    2005-01-01

    We present single-mode solid-state polymer dye lasers fabricated with standard UV lithography. The lasers use a high-order Bragg grating and rely on index-tuning of a photosensitive polymer for waveguiding. The gain medium is Rhodamine 6G.......We present single-mode solid-state polymer dye lasers fabricated with standard UV lithography. The lasers use a high-order Bragg grating and rely on index-tuning of a photosensitive polymer for waveguiding. The gain medium is Rhodamine 6G....

  15. 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.

    Science.gov (United States)

    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. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Enhanced adsorption of active brilliant red X-3B dye on chitosan molecularly imprinted polymer functionalized with Ti(IV) as Lewis acid.

    Science.gov (United States)

    Deng, Hui; Wei, Zhilai; Wang, XiaoNing

    2017-02-10

    A Ti(IV) functionalized chitosan molecularly imprinted polymer (Ti-CSMIP) was successfully prepared. Ti 4+ as Lewis acidic was used to modify chitosan MIP by producing metal hydroxyl group and protonated surface of adsorbent in aqueous solution to recognize X-3B molecule as a Lewis base. The adsorbent was characterized by FTIR, SEM, XRD, BET, elemental and zeta potential analysis. XRD illustrated Ti-CSMIP exhibited a weak anatase phase when Ti 4+ cross-linked with chitosan. Batch adsorption experiments were performed to evaluate adsorption condition, including sorption isotherm, kinetics and reusability. The maximum adsorption capacity of Ti-CSMIP for X-3B was 161.1mg/g at 293K when solution pH was in the range of 6.0-7.0. Equilibrium data was well analyzed by three-parameter isotherm model, and the kinetics of adsorption followed the pseudo-second kinetics equation. Regeneration experiments indicated a possible application as an effective sorbent for the selective removal of azo anionic dye in aqueous solutions. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Dye-sensitized solar cell with natural gel polymer electrolytes and f-MWCNT as counter-electrode

    Science.gov (United States)

    Nwanya, A. C.; Amaechi, C. I.; Ekwealor, A. B. C.; Osuji, R. U.; Maaza, M.; Ezema, F. I.

    2015-05-01

    Samples of DSSCs were made with gel polymer electrolytes using agar, gelatin and DNA as the polymer hosts. Anthocyanine dye from Hildegardia barteri flower is used to sensitize the TiO2 electrode, and the spectrum of the dye indicates strong absorptions in the blue region of the solar spectrum. The XRD pattern of the TiO2 shows that the adsorption of the dye did not affect the crystallinity of the electrode. The f-MWCNT indicates graphite structure of the MWCNTs were acid oxidized without significant damage. Efficiencies of 3.38 and 0.1% were obtained using gelatin and DNA gel polymer electrolytes, respectively, for the fabricated dye-sensitized solar cells.

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

    Science.gov (United States)

    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. Implementation of all-optical reversible logic gate based on holographic laser induced grating using azo-dye doped polymers

    Science.gov (United States)

    Forsati, Rana; Valipour Ebrahimi, Sara; Navi, Keivan; Mohajerani, Ezeddin; Jashnsaz, Hossein

    2013-02-01

    Increasing demand for power reduction in computer systems has led to new trends in computations and computer design including reversible computing. Its main aim is to eliminate power dissipation in logical elements but can have some other advantages such as data security and error prevention. Because of interesting properties of reversible computing, implementing computing devices with reversible manner is the only way to make the reversible computing a reality. In recent years, reversible logic has turned out to be a promising computing paradigm having application in CMOS, nanotechnology, quantum computing and optical computing. In this paper, we propose and realize a novel implementation of Toffoli gate in all-optical domain. We have explained its principle of operations and described an actual experimental implementation. The all-optical reversible gate presented in this paper will be useful in different applications such as arithmetic and logical operations in the domain of reversible logic-based computing.

  20. A UV-prepared linear polymer electrolyte membrane for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Imperiyka, M., E-mail: imperiyka@gmail.com [Faculty of Arts and Sciences, Kufra Campus, University of Benghazi, Al Kufrah (Libya); Ahmad, A.; Hanifah, S.A. [School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Polymer Research Center, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Bella, F. [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento 21, 10129 Torino (Italy); Department of Applied Science and Technology – DISAT, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Torino (Italy)

    2014-10-01

    The effects of LiClO{sub 4} and LiFS{sub 3}SO{sub 3} on poly(glycidyl methacrylate)-based solid polymer electrolyte and its photoelectrochemical performance in a dye sensitized solar cell consisting of FTO/TiO{sub 2}–dye/P(GMA)–LiClO{sub 4}–EC/Pt were investigated. The electrochemical stability of films was studied by cyclic voltammetry (CV). The highest ionic conductivities obtained were 4.2×10{sup −5} and 3.7×10{sup −6} S cm{sup −1} for the film containing 30 wt% LiClO{sub 4} and 25 wt% LiCF{sub 3}SO{sub 3}, respectively. The polymer electrolytes showed electrochemical stability windows up to 3 V and 2.8 V for LiClO{sub 4} and LiCF{sub 3}SO{sub 3}, respectively. The assembled dye-sensitized solar cell showed a sunlight conversion efficiency of 0.679% (J{sub sc}=3 mA cm{sup −2}, V{sub oc}=0.48 V and FF=0.47), under light intensity of 100 mW cm{sup −2}.

  1. Development of a Chemiresistor Sensor Based on Polymers-Dye Blend for Detection of Ethanol Vapor

    Directory of Open Access Journals (Sweden)

    Marcos A. L. dos Reis

    2010-03-01

    Full Text Available The conductive blend of the poly (3,4-ethylene dioxythiophene and polystyrene sulfonated acid (PEDOT-PSS polymers were doped with Methyl Red (MR dye in the acid form and were used as the basis for a chemiresistor sensor for detection of ethanol vapor. This Au│Polymers-dye blend│Au device was manufactured by chemical vapor deposition and spin-coating, the first for deposition of the metal electrodes onto a glass substrate, and the second for preparation of the organic thin film forming ~1.0 mm2 of active area. The results obtained are the following: (i electrical resistance dependence with atmospheres containing ethanol vapor carried by nitrogen gas and humidity; (ii sensitivity at 1.15 for limit detection of 26.25 ppm analyte and an operating temperature of 25 °C; and (iii the sensing process is quickly reversible and shows very a low power consumption of 20 μW. The thin film morphology of ~200 nm thickness was analyzed by Atomic Force Microscopy (AFM, where it was observed to have a peculiarly granulometric surface favorable to adsorption. This work indicates that PEDOT-PSS doped with MR dye to compose blend film shows good performance like resistive sensor.

  2. Photoinduced charge and energy transfer in dye-doped conjugated polymers

    International Nuclear Information System (INIS)

    Veldman, Dirk; Bastiaansen, Jolanda J.A.M.; Langeveld-Voss, Bea M.W.; Sweelssen, Joergen; Koetse, Marc M.; Meskers, Stefan C.J.; Janssen, Rene A.J.

    2006-01-01

    Conjugated polymer-molecular dye blends of MDMO-PPV (poly[2-methoxy-5-(3',7'-dimethyloctyloxy)-1,4-phenylenevinylene]) and PF1CVTP (poly[9,9-dioctylfluorene-2,7-diyl-alt-2,5-bis(2-thienyl-1-cyanovinyl) -1-(3',7= '-dimethyloctyloxy)-4-methoxybenzene-5'',5''-diyl]) with three dipyrrometheneboron difluoride (bodipy) dyes were studied by (time-resolved) fluorescence and photoinduced absorption spectroscopy to determine quantitatively the relation between the electronic HOMO and LUMO levels and the occurrence of energy or charge transfer after optical excitation. We find that for MDMO-PPV photoinduced charge transfer to the dyes occurs, while photoexcitation of PF1CVTP exclusively results in energy transfer. The differences can be rationalized by assuming that the energy of the charge separated state is 0.33-0.45 eV higher than the energy determined from oxidation and reduction potentials of donor and acceptor, respectively. This provides an important design rule to identify appropriate materials for polymer solar cells that can have a high open-circuit voltage

  3. Ozo-Dyes mixture degradation in a fixed bed biofilm reactor packed with volcanic porous rock

    International Nuclear Information System (INIS)

    Contreras-Blancas, E.; Cobos-Vasconcelos, D. de los; Juarez-Ramirez, C.; Poggi-Varaldo, H. M.; Ruiz-Ordaz, N.; Galindez-Mayer, J.

    2009-01-01

    Textile industries discharge great amounts of dyes and dyeing-process auxiliaries, which pollute streams and water bodies. Several dyes, especially the ones containing the azo group, can cause harmful effects to different organisms including humans. Through bacterial and mammalian tests, azo dyes or their derived aromatic amines have shown cell genotoxicity. The purpose of this work was to evaluate the effect of air flow rate on azo-dyes mixture biodegradation by a microbial community immobilized in a packed bed reactor. (Author)

  4. Ozo-Dyes mixture degradation in a fixed bed biofilm reactor packed with volcanic porous rock

    Energy Technology Data Exchange (ETDEWEB)

    Contreras-Blancas, E.; Cobos-Vasconcelos, D. de los; Juarez-Ramirez, C.; Poggi-Varaldo, H. M.; Ruiz-Ordaz, N.; Galindez-Mayer, J.

    2009-07-01

    Textile industries discharge great amounts of dyes and dyeing-process auxiliaries, which pollute streams and water bodies. Several dyes, especially the ones containing the azo group, can cause harmful effects to different organisms including humans. Through bacterial and mammalian tests, azo dyes or their derived aromatic amines have shown cell genotoxicity. The purpose of this work was to evaluate the effect of air flow rate on azo-dyes mixture biodegradation by a microbial community immobilized in a packed bed reactor. (Author)

  5. Optoelectronic and Photovoltaic Performances of Pyridine Based Monomer and Polymer Capped ZnO Dye-Sensitized Solar Cells.

    Science.gov (United States)

    Singh, Satbir; Raj, Tilak; Singh, Amarpal; Kaur, Navneet

    2016-06-01

    The present research work describes the comparative analysis and performance characteristics of 4-pyridine based monomer and polymer capped ZnO dye-sensitized solar cells. The N, N-dimethyl-N4-((pyridine-4yl)methylene) propaneamine (4,monomer) and polyamine-4-pyridyl Schiff base (5, polymer) dyes were synthesized through one step condensation reaction between 4-pyridinecarboxaldehyde 1 and N, N-dimethylpropylamine 2/polyamine 3. Products obtained N, N-dimethyl-N4-((pyridine-4yl)methylene)propaneamine (4) and polyamine-4-pyridyl Schiff base (5) were purified and characterized using 1H, 13C NMR, mass, IR and CHN spectroscopy. Both the dyes 4 and 5 were further coated over ZnO nanoparticles and characterized using SEM, DLS and XRD analysis. Absorption profile and emission profile was monitored using fluorescence and UV-Vis absorption spectroscopy. A thick layer of these inbuilt dye linked ZnO nanoparticles of dyes (4) and (5) was pasted on one of the conductive side of ITO glass followed with a liquid electrolyte and counter electrode of the same conductive glass. Polyamine-4-pyridyl Schiff base polymer (5) decorated dye sensitized solar cell has shown better exciting photovoltaic properties in the form of short circuit current density (J(sc) = 6.3 mA/cm2), open circuit photo voltage (V(oc) = 0.7 V), fill factor (FF = 0.736) than monomer decorated dye sensitized solar cell. Polymer dye (5) based ZnO solar cell has shown a maximum solar power to electrical conversion efficiency of 3.25%, which is enhanced by 2.16% in case of monomer dye based ZnO solar cell under AM 1.5 sun illuminations.

  6. Degradation of the azo dye Acid Red 1 by anodic oxidation and indirect electrochemical processes based on Fenton's reaction chemistry. Relationship between decolorization, mineralization and products

    International Nuclear Information System (INIS)

    Florenza, Xavier; Solano, Aline Maria Sales; Centellas, Francesc; Martínez-Huitle, Carlos Alberto

    2014-01-01

    Highlights: • Degradation of Acid Red 1 by anodic oxidation, electro-Fenton and photoelectro-Fenton • Quicker and similar decolorization by electro-Fenton and photoelectro-Fenton due to oxidation with ● OH in the bulk • Almost total mineralization by photoelectro-Fenton with Pt or BDD due to fast photolysis of products by UVA light • Detection of 11 aromatic products, 15 hydroxylated compounds, 13 desulfonated derivatives and 7 carboxylic acids • Release of NH 4 + , NO 3 − and SO 4 2− ions, and generation of persistent N-products of low molecular mass - Abstract: Solutions of 236 mg dm −3 Acid Red 1 (AR1), an azo dye widely used in textile dying industries, at pH 3.0 have been comparatively treated by anodic oxidation with electrogenerated H 2 O 2 (AO-H 2 O 2 ), electro-Fenton (EF) and photoelectro-Fenton (PEF) at constant current density (j). Assays were performed with a stirred tank reactor equipped with a Pt or boron-doped diamond (BDD) anode and an air-diffusion cathode for H 2 O 2 generation from O 2 reduction. The main oxidizing agents were hydroxyl radicals produced at the anode from water oxidation in all methods and in the bulk from Fenton's reaction between generated H 2 O 2 and 0.5 mmol dm −3 Fe 2+ in EF and PEF. For each anode, higher oxidation power was found in the sequence AO-H 2 O 2 < EF < PEF. The oxidation ability of the BDD anode was always superior to that of Pt. Faster and similar decolorization efficiency was achieved in EF and PEF owing to the quicker destruction of aromatics with hydroxyl radicals produced in the bulk. The PEF process with BDD was the most potent method yielding almost total mineralization due to the additional rapid photolysis of recalcitrant intermediates like Fe(III)-carboxylate complexes under UVA irradiation. The increase in j always enhanced the decolorization and mineralization processes because of the greater production of hydroxyl radicals, but decreases the mineralization current efficiency

  7. High-throughput measurement of polymer film thickness using optical dyes

    Science.gov (United States)

    Grunlan, Jaime C.; Mehrabi, Ali R.; Ly, Tien

    2005-01-01

    Optical dyes were added to polymer solutions in an effort to create a technique for high-throughput screening of dry polymer film thickness. Arrays of polystyrene films, cast from a toluene solution, containing methyl red or solvent green were used to demonstrate the feasibility of this technique. Measurements of the peak visible absorbance of each film were converted to thickness using the Beer-Lambert relationship. These absorbance-based thickness calculations agreed within 10% of thickness measured using a micrometer for polystyrene films that were 10-50 µm. At these thicknesses it is believed that the absorbance values are actually more accurate. At least for this solvent-based system, thickness was shown to be accurately measured in a high-throughput manner that could potentially be applied to other equivalent systems. Similar water-based films made with poly(sodium 4-styrenesulfonate) dyed with malachite green oxalate or congo red did not show the same level of agreement with the micrometer measurements. Extensive phase separation between polymer and dye resulted in inflated absorbance values and calculated thickness that was often more than 25% greater than that measured with the micrometer. Only at thicknesses below 15 µm could reasonable accuracy be achieved for the water-based films.

  8. Photoluminescence Spectroscopy of Rhodamine 800 Aqueous Solution and Dye-Doped Polymer Thin-Film: Concentration and Solvent Effects

    Science.gov (United States)

    Le, Khai Q.; Dang, Ngo Hai

    2018-05-01

    This paper investigates solvent and concentration effects on photoluminescence (PL) or fluorescence properties of Rhodamine 800 (Rho800) dyes formed in aqueous solution and polymer thin-film. Various commonly used organic solvents including ethanol, methanol and cyclopentanol were studied at a constant dye concentration. There were small changes in the PL spectra for the different solvents in terms of PL intensity and peak wavelength. The highest PL intensity was observed for cyclopentanol and the lowest for ethanol. The longest peak wavelength was found in cyclopentanol (716 nm) and the shortest in methanol (708 nm). Dissolving the dye powder in the methanol solvent and varying the dye concentration in aqueous solution from the high concentrated solution to highly dilute states, the wavelength tunability was observed between about 700 nm in the dilute state and 730 nm at high concentration. Such a large shift may be attributed to the formation of dye aggregates. Rho800 dye-doped polyvinyl alcohol (PVA) polymer thin-film was further investigated. The PL intensity of the dye in the form of thin-film is lower than that of the aqueous solution form whereas the peak wavelength is redshifted due to the presence of PVA. This paper, to our best knowledge, reports the first study of spectroscopic properties of Rho800 dyes in various forms and provides useful guidelines for production of controllable organic luminescence sources.

  9. Polymer-Optical-Fiber Lasers and Amplifiers Doped with Organic Dyes

    Directory of Open Access Journals (Sweden)

    Joseba Zubia

    2011-07-01

    Full Text Available Polymer optical fibers (POFs doped with organic dyes can be used to make efficient lasers and amplifiers due to the high gains achievable in short distances. This paper analyzes the peculiarities of light amplification in POFs through some experimental data and a computational model capable of carrying out both power and spectral analyses. We investigate the emission spectral shifts and widths and on the optimum signal wavelength and pump power as functions of the fiber length, the fiber numerical aperture and the radial distribution of the dopant. Analyses for both step-index and graded-index POFs have been done.

  10. Recycling of negative electrodes from spent Ni-Cd batteries as CdO with nanoparticle sizes and its application in remediation of azo dye

    Energy Technology Data Exchange (ETDEWEB)

    Moreira, T.F.M.; Santana, I.L.; Moura, M.N.; Ferreira, S.A.D.; Lelis, M.F.F.; Freitas, M.B.J.G., E-mail: marcosbj@hotmail.com

    2017-07-01

    In this study, negative electrodes from spent Ni-Cd batteries were recycled as CdCO{sub 3}, which was thermally treated to produce synthetized, nanostructured CdO. There is interest in CdO because of its energy band gap, high electrical conductivity and selective catalytic properties. CdO was characterized in this study by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and transmission electronic microscopy (TEM). The XRD pattern showed CdO peaks in a crystalline cubic phase, and the average crystallite diameter was 22.21 nm. TEM micrographs showed the formation of clusters containing nanostructures. We also tested the efficiency of CdO catalytic activity in degrading Reactive Black 5 (RB5) dye. Degradation was conducted in conditions of pH = 4.0, pH = 5.97 and pH = 8.0. The degradation efficiency was, respectively, 65.42%, 61.80% and 67.01% after 480 min of reaction. The determining step in the reaction mechanism for dye degradation was the formation of the radical ion OH·. Therefore, the degradation exhibited a first-order reaction. The catalytic activity of CdO and the rate constant values were independent of the pH of the solution. This work presents potential solutions for two environmental problems: recycling Cd and dye degradation. - Graphical abstract: Recycling of spent Ni-Cd batteries as CdO nanoparticles. - Highlights: • This work presents solutions for Cd recycling and dye degradation. • Anodes of Ni-Cd batteries were recycled as CdO with nanometer-sized particles. • CdO presents catalytic activity in the degradation of reactive black dye. • Decoloration of reactive black dye exhibits first-order reaction. • The rate constant values are independent of the pH solution.

  11. High stability of polymer optical fiber with dye doped cladding for illumination systems

    Energy Technology Data Exchange (ETDEWEB)

    Jaramillo-Ochoa, L. [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Querétaro 76230, México (Mexico); Narro-García, R. [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Querétaro 76230, México (Mexico); Universidad Autónoma de Chihuahua, Facultad de Ingeniería, Circuito Universitario S/N, 31125 Chihuahua, Chih., México (Mexico); Ocampo, M.A. [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Querétaro 76230, México (Mexico); Quintero-Torres, R., E-mail: rquintero@fata.unam.mx [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Querétaro 76230, México (Mexico)

    2017-04-15

    In this work, the photodegradation of a polymer optical fiber with Rhodamine doped cladding as a function of illumination time and excitation intensity is presented. To show the effect of photodegradation on different bulk geometries and environments, the photodegradation from a dye doped preform and a PMMA thick film is also evaluated. The reversible and the irreversible degradation of the florescent material were quantified under an established excitation scheme. To this purpose, a four-level system to model the photodegradation rates and its relation with the population of the states is presented and it is used to justify a possible underlying mechanism. The obtained results suggest an increase of one order of magnitude in the stability (lifetime) of the polymer optical fiber with respect to the preform or the thick film geometry stability.

  12. Novel amphiphilic polymeric ionic liquid-solid phase micro-extraction membrane for the preconcentration of aniline as degradation product of azo dye Orange G under sonication by liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Cai, Mei-Qiang; Wei, Xiao-Qing; Du, Chun-Hui; Ma, Xu-Ming; Jin, Mi-Cong

    2014-07-04

    A novel amphiphilic polymeric ionic liquid membrane containing a hydrophilic bromide anion and a hydrophobic carbonyl group was synthesized in dimethylformamide (DMF) systems using the ionic liquid 1-butyl-3-vinylimidazolium bromide (BVImBr) and the methylmethacrylate (MMA) as monomers. The prepared amphiphilic ploy-methylmethacrylate-1-butyl-3-vinylimidazolium bromide (MMA-BVImBr) was characterized by a scanning electron microscope and an infrared spectrum instrument. The results of solid-phase micro-extraction membrane (SPMM) experiments showed that the adsorption capacity of membrane was about 0.76μgμg(-1) for aniline. Based on this, a sensitive method for the determination of trace aniline, as a degradation product of azo dye Orange G under sonication, was developed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The calibration curve showed a good linearity ranging from 0.5 to 10.0μgL(-1) with a correlation coefficient value of 0.9998. The limit of quantification was 0.5μgL(-1). The recoveries ranged from 90.6% to 96.1%. The intra- and inter-day relative standard deviations were less than 8.3% and 10.9%. The developed SPMM-LC-MS/MS method was used successfully for preconcentration of trace aniline produced during the sonication of Orange G solution. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Cobalt ferrite nano-composite coated on glass by Doctor Blade method for photo-catalytic degradation of an azo textile dye Reactive Red 4: XRD, FESEM and DRS investigations.

    Science.gov (United States)

    Habibi, Mohammad Hossein; Parhizkar, Janan

    2015-11-05

    Cobalt ferrite nano-composite was prepared by hydrothermal route using cobalt nitrate, iron nitrate and ethylene glycol as chelating agent. The nano-composite was coated on glass by Doctor Blade method and annealed at 300 °C. The structural, optical, and photocatalytic properties have been studied by powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and UV-visible spectroscopy (UV-Vis DRS). Powder XRD analysis confirmed formation of CoFe2O4 spinel phase. The estimated particle size from FESEM data was 50 nm. The calculated energy band gaps, obtained by Tauc relation from UV-Vis absorption spectra was 1.3 eV. Photocatalytic degradation of Reactive Red 4 as an azo textile was investigated in aqueous solution under irradiation showed 68.0% degradation of the dye within 100 min. The experimental enhanced activity compare to pure Fe2O3 can be ascribed to the formation of composite, which was mainly attributable to the transfer of electron and hole to the surface of composite and hinder the electron hole recombination. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. Ni/MgAlO regeneration for catalytic wet air oxidation of an azo-dye in trickle-bed reaction

    International Nuclear Information System (INIS)

    Vallet, Ana; Ovejero, Gabriel; Rodríguez, Araceli; Peres, José A.; García, Juan

    2013-01-01

    Highlights: ► Ni supported over hydrotalcite calcined precursors as catalyst. ► Catalytic wet air oxidation in trickle bed reactor for Chromotrope 2R removal. ► Dye removal depends on temperature, initial dye concentration and flow rate. ► The catalyst proved to bare-usable after in situ regeneration. -- Abstract: Active nickel catalysts (7 wt%) supported over Mg–Al mixed oxides have been recently developed and it has also been demonstrated that they are also highly selective in Catalytic Wet air Oxidation (CWAO) of dyes. CWAO of Chromotrope 2R (C2R) has been studied using a trickle bed reactor employing temperatures from 100 to 180 °C, liquid flow rates from 0.1 to 0.7 mL min −1 and initial dye concentration from 10 to 50 ppm. Total pressure and air flow were 25 bar and 300 mL min −1 , respectively. The catalyst showed a very stable activity up to 24 h on stream with an average TOC conversion of 82% at 150 °C and T r = 0.098 g Ni min mL −1 . After the reaction, a 1.1 wt% C of carbonaceous deposit is formed onto the catalyst and a diminution of 30% of the surface area with respect of the fresh catalyst was observed. An increase in the space time gave higher TOC conversions up to T r = 0.098 g Ni min mL −1 , attaining values of 80% at 180 °C. The performance of TOC and dye removal does not decrease after two regeneration cycles. In total, a 57 h effective reaction has been carried out with no loss of catalytic activity

  15. Ni/MgAlO regeneration for catalytic wet air oxidation of an azo-dye in trickle-bed reaction

    Energy Technology Data Exchange (ETDEWEB)

    Vallet, Ana [Grupo de Catálisis y Procesos de Separación (CyPS), Departamento de Ingeniería Química, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Ovejero, Gabriel, E-mail: govejero@quim.ucm.es [Grupo de Catálisis y Procesos de Separación (CyPS), Departamento de Ingeniería Química, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Rodríguez, Araceli [Grupo de Catálisis y Procesos de Separación (CyPS), Departamento de Ingeniería Química, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain); Peres, José A. [Centro de Química de Vila Real, Universidade de Trás-os-Montes e Alto Douro, Apartado 1013, 5001-801 Vila Real (Portugal); García, Juan, E-mail: juangcia@quim.ucm.es [Grupo de Catálisis y Procesos de Separación (CyPS), Departamento de Ingeniería Química, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid (Spain)

    2013-01-15

    Highlights: ► Ni supported over hydrotalcite calcined precursors as catalyst. ► Catalytic wet air oxidation in trickle bed reactor for Chromotrope 2R removal. ► Dye removal depends on temperature, initial dye concentration and flow rate. ► The catalyst proved to bare-usable after in situ regeneration. -- Abstract: Active nickel catalysts (7 wt%) supported over Mg–Al mixed oxides have been recently developed and it has also been demonstrated that they are also highly selective in Catalytic Wet air Oxidation (CWAO) of dyes. CWAO of Chromotrope 2R (C2R) has been studied using a trickle bed reactor employing temperatures from 100 to 180 °C, liquid flow rates from 0.1 to 0.7 mL min{sup −1} and initial dye concentration from 10 to 50 ppm. Total pressure and air flow were 25 bar and 300 mL min{sup −1}, respectively. The catalyst showed a very stable activity up to 24 h on stream with an average TOC conversion of 82% at 150 °C and T{sub r} = 0.098 g{sub Ni} min mL{sup −1}. After the reaction, a 1.1 wt% C of carbonaceous deposit is formed onto the catalyst and a diminution of 30% of the surface area with respect of the fresh catalyst was observed. An increase in the space time gave higher TOC conversions up to T{sub r} = 0.098 g{sub Ni} min mL{sup −1}, attaining values of 80% at 180 °C. The performance of TOC and dye removal does not decrease after two regeneration cycles. In total, a 57 h effective reaction has been carried out with no loss of catalytic activity.

  16. Treatment of azo dye-containing wastewater by a Fenton-like process in a continuous packed-bed reactor filled with activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Mesquita, Isabel; Matos, Luis C. [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); Duarte, Filipa [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal); Maldonado-Hodar, F.J. [Department of Inorganic Chemistry, Faculty of Sciences, University of Granada, Av. Fuentenueva, 18071 Granada (Spain); Mendes, Adelio [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal); Madeira, Luis M., E-mail: mmadeira@fe.up.pt [Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); LEPAE - Laboratory for Process, Environmental and Energy Engineering, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Porto (Portugal)

    2012-10-30

    Highlights: Black-Right-Pointing-Pointer Oxidation with the Fenton's reagent was carried out in a packed-bed reactor. Black-Right-Pointing-Pointer The packed-bed was filled with iron-impregnated activated carbon. Black-Right-Pointing-Pointer The increment of temperature increases the Chicago Sky Blue removal and mineralization. Black-Right-Pointing-Pointer The values of iron leaching were below 0.4 ppm in the outlet effluent. Black-Right-Pointing-Pointer It was possible to reach a dye conversion of 88% in steady-state. - Abstract: In this work, oxidation with a Fenton-like process of a dye solution was carried out in a packed-bed reactor. Activated carbon Norit RX 3 Extra was impregnated with ferrous sulfate and used as catalyst (7 wt.% of iron). The effect of the main operating conditions in the Chicago Sky Blue (CSB) degradation was analyzed. It was found that the increase in temperature leads to a higher removal of the dye and an increased mineralization. However, it also increases the iron leaching, but the values observed were below 0.4 ppm (thus, far below European Union limits). It was possible to reach, at steady-state, a dye conversion of 88%, with a total organic carbon (TOC) removal of ca. 47%, being the reactor operated at 50 Degree-Sign C, pH 3, W{sub cat}/Q = 4.1 g min mL{sup -1} (W{sub cat} is the mass of catalyst and Q the total feed flow rate) and a H{sub 2}O{sub 2} feed concentration of 2.25 mM (for a CSB feed concentration of 0.012 mM). The same performance was reached in three consecutive cycles.

  17. Solidification of liquid electrolyte with imidazole polymers for quasi-solid-state dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Wang Miao; Lin Yuan; Zhou Xiaowen; Xiao Xurui; Yang Lei; Feng Shujing; Li Xueping

    2008-01-01

    Quasi-solid-state electrolytes were prepared by employing the imidazole polymers to solidify the liquid electrolyte containing lithium iodide, iodine and ethylene carbonate (EC)/propylene carbonate (PC) mixed solvent. The ionic conductivity and diffusion behavior of triiodide in the quasi-solid-state electrolytes were examined in terms of the polymer content. Application of the quasi-solid-state electrolytes to the dye-sensitized solar cells, the maximum energy conversion efficiency of 7.6% (AM 1.5, 100 mW cm -2 ) was achieved. The dependence of the photovoltaic performance on the polymer content and on the different anions of the imidazole polymers was studied by electrochemical impedance spectroscopy and cyclic voltammetry. The results indicate the charge transfer behaviors occurred at nanocrystalline TiO 2 /electrolyte and Pt/electrolyte interface play an important role in influencing the photovoltaic performance of quasi-solid-state dye-sensitized solar cells

  18. In vitro mutagenicity, NMR metabolite characterization of azo and triphenylmethanes dyes by adherents bacteria and the role of the "cna" adhesion gene in activated sludge.

    Science.gov (United States)

    Ayed, Lamia; Bakir, Karima; Ben Mansour, Hedi; Hammami, Saousen; Cheref, Abdelkrim; Bakhrouf, Amina

    2017-02-01

    Staphylococcus aureus, showing the greatest decolorization ability, was further investigated for Methyl Red (MR) Congo Red (CR), Crystal Violet (CV) and Malachite Green (MG) decolorization using response surface methodology (RSM). The chemometric methods use, based on statistical design of experiments (DOEs) such as RSM is becoming increasingly widespread in several sciences such as analytical chemistry, engineering and environmental chemistry. Stapphylococcus aureus ATCC 25923, Stapphylococcus aureus (S1) and Stapphylococcus aureus (S2), were isolated from textile wastewater plant located in KsarHellal, Tunisia and were tested for their decolorization capacity. PCR technique was utilized to identify the 3 bacterial strains and to detect the adhesin gene "cna". Biodegradation of MR, CR, CV and MG (750 ppm), were investigated under shaking condition in Mineral Salt Medium (MSM) solution at pH 7.5 and temperature 30 °C, using a 3.7 × 10 5  CFU/ml as inoculum size. Our results showed that Staphylococcus aureus had a high decolorization capacity. Nuclear magnetic resonance (NMR) spectroscopy analysis confirmed the biodegradation of dyes. The four dyes mutagenicity with the S9 metabolizing system decreased significantly after biodegradation and totally disappeared. Nuclear magnetic resonance (NMR) spectroscopy analysis confirmed the biodegradation of dyes. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Ni/MgAlO regeneration for catalytic wet air oxidation of an azo-dye in trickle-bed reaction.

    Science.gov (United States)

    Vallet, Ana; Ovejero, Gabriel; Rodríguez, Araceli; Peres, José A; García, Juan

    2013-01-15

    Active nickel catalysts (7 wt%) supported over Mg-Al mixed oxides have been recently developed and it has also been demonstrated that they are also highly selective in Catalytic Wet air Oxidation (CWAO) of dyes. CWAO of Chromotrope 2R (C2R) has been studied using a trickle bed reactor employing temperatures from 100 to 180 °C, liquid flow rates from 0.1 to 0.7 mL min(-1) and initial dye concentration from 10 to 50 ppm. Total pressure and air flow were 25 bar and 300 mL min(-1), respectively. The catalyst showed a very stable activity up to 24 h on stream with an average TOC conversion of 82% at 150 °C and T(r)=0.098 g(Ni) min mL(-1). After the reaction, a 1.1 wt% C of carbonaceous deposit is formed onto the catalyst and a diminution of 30% of the surface area with respect of the fresh catalyst was observed. An increase in the space time gave higher TOC conversions up to T(r)=0.098 g(Ni) min mL(-1), attaining values of 80% at 180 °C. The performance of TOC and dye removal does not decrease after two regeneration cycles. In total, a 57 h effective reaction has been carried out with no loss of catalytic activity. Copyright © 2012 Elsevier B.V. All rights reserved.

  20. Dye-Incorporated Polynaphthalenediimide Acceptor for Additive-Free High-Performance All-Polymer Solar Cells.

    Science.gov (United States)

    Chen, Dong; Yao, Jia; Chen, Lie; Yin, Jingping; Lv, Ruizhi; Huang, Bin; Liu, Siqi; Zhang, Zhi-Guo; Yang, Chunhe; Chen, Yiwang; Li, Yongfang

    2018-04-16

    All-polymer solar cells (all-PSCs) can offer unique advantages for applications in flexible devices, and naphthalene diimide (NDI)-based polymer acceptors are the widely used polymer acceptors. However, their power conversion efficiency (PCE) still lags behind that of state-of-the-art polymer solar cells, due to low light absorption, suboptimal energy levels and the strong aggregation of the NDI-based polymer acceptor. Herein, a rhodanine-based dye molecule was introduced into the NDI-based polymer acceptor by simple random copolymerization and showed an improved light absorption coefficient, an up-shifted lowest unoccupied molecular orbital level and reduced crystallization. Consequently, additive-free all-PSCs demonstrated a high PCE of 8.13 %, which is one of the highest performance characteristics reported for all-PSCs to date. These results indicate that incorporating a dye into the n-type polymer gives insight into the precise design of high-performance polymer acceptors for all-PSCs. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Dye-sensitized solar cells and solar module using polymer electrolytes: Stability and performance investigations

    Directory of Open Access Journals (Sweden)

    Jilian Nei de Freitas

    2006-01-01

    Full Text Available We present recent results on solid-state dye-sensitized solar cell research using a polymer electrolyte based on a poly(ethylene oxide derivative. The stability and performance of the devices have been improved by a modification in the method of assembly of the cells and by the addition of plasticizers in the electrolyte. After 30 days of solar irradiation (100 mW cm-2 no changes in the cell's efficiency were observed using this new method. The effect of the active area size on cell performance and the first results obtained for the first solar module composed of 4.5 cm2 solid-state solar cells are also presented.

  2. Influence of generated intermediates’ interaction on heterogeneous Fenton's degradation of an azo dye 1-diazo-2-naphthol-4-sulfonic acid by using sludge based carbon as catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Gu, Lin [School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093 (China); School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Huang, Shouqiang [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Zhu, Nanwen, E-mail: nwzhu@sjtu.edu.cn [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Zhang, Daofang, E-mail: Zhangdf-usst@163.com [School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093 (China); Yuan, Haiping; Lou, Ziyang [School of Environmental Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2013-12-15

    Highlights: • End-products have higher tendency to be adsorbed on SC than primarily-formed. • Higher initial H{sub 2}O{sub 2} dosage results in intermediates with strong polarity. • 9 model intermediates differ in their behavior on interactions with catalysts. • Polar surface area dominated their adsorption on SC while K{sub ow} acts as a key role on HSC. -- Abstract: Sewage sludge based carbons have recently been used as novel catalyst in heterogeneous Fenton's reactions to degrade azo dye molecules. The carbons, functioning as both catalyst and adsorbent, play an important role in pollutants elimination, especially for those simultaneously generated organic intermediates. Different factors, i.e., H{sub 2}O{sub 2} concentration, may influence the type and properties of those intermediates and may have great impacts on their elimination through the interactions with catalysts’ surface. Thus, techniques including Temperature Programmed Desorption-Mass Spectrometer (TPD-MS), N{sub 2} adsorption isotherm and Scanning Electron Microscope (SEM) were used to probe the ways of the interaction between oxidation products and catalyst by using different initial H{sub 2}O{sub 2} concentrations (10 and 20 mM). The higher Chemical Oxygen Demand (COD) removal with 20 mM H{sub 2}O{sub 2} was found to be related not only to the higher hydroxyl radicals but also the specific interactions between the intermediates and catalyst’ surface. The deep oxidation occurred in the conditions with higher oxidant amount enhances the intermediates’ adsorption on catalyst, thus increasing the COD removal by large margin. Simulated adsorption experiments by using six primarily formed intermediates and three deeply mineralized products on three different catalysts also confirmed the assumption. Results suggested close relations between adsorption capacities and intermediates’ properties such as polar surface area and octanol-water partition coefficient.

  3. Combined cation-exchange and solid phase extraction for the selective separation and preconcentration of zinc, copper, cadmium, mercury and cobalt among others using azo-dye functionalized resin.

    Science.gov (United States)

    Chatterjee, Mousumi; Srivastava, Bhavya; Barman, Milan K; Mandal, Bhabatosh

    2016-04-01

    A facile synthesis of an ion exchange material (FSG-PAN) has been achieved by functionalizing silica gel with an azo-dye. Its composition and structure are well assessed by systematic analysis. Extractor possesses high BET surface area (617.794m(2)g(-1)), exchange capacity and break-through capacity (BTC) (Q0 Zn(II): 225; Cd(II): 918; Hg(II): 384, Cu(II): 269 and Co(II): 388μMg(-1)). The sorption process was endothermic (+ΔH), entropy-gaining (+ΔS) and spontaneous (-ΔG) in nature. Preconcentration factor has been optimized at 172(Zn(II)); 157.2(Cd(II)); 193.6(Hg(II)); 176(Cu(II)); 172.4(Co(II)). Density functional theory calculation has been performed to analyze the sorption pathway. BTC (μMg(-1)) of FSG-PAN was found to be the product of its frontier orbitals and state of sorbed metal ion species, x (at x=1, mononuclear and x>1, a polynuclear species; i.e., BTC=[amount of HOMO]×x). FSG-PAN is used for the selective separation and preconcentration of Zn(II), Cd(II), Hg(II), Cu(II),Co(II) from large volume sample (800mL) of low concentration (0.017-0.40mML(-1)) in presence of foreign ions (50-300mML(-1)) at optimum conditions (pH: 7.0±1.5, flow rate: 2.5mLmin(-1), temperature: 27°C, equilibration-time: 5min). The method was found to be effective for real samples also. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Two Chemically Stable Cd(II Polymers as Fluorescent Sensor and Photocatalyst for Aromatic Dyes

    Directory of Open Access Journals (Sweden)

    Jun Wang

    2018-03-01

    Full Text Available Two new 2D Cd(II-based coordination polymers (CPs, viz. [Cd2(H2L2(2,2’-bipy2] (1 and [Cd(L0.5(phen·0.5H2O] (2, have been constructed using ethylene glycol ether bridging tetracarboxylate ligand 5,5′(4,4′-phenylenebis(methyleneoxy diisophthalic acid (H4L. Both CPs behaved as profound fluorescent sensor for Fe3+ ion and nitro-aromatics (NACs, specifically 2,4,6-trinitrophenol (TNP. The stability at elevated temperature and photocatalytic behaviors of both 1 and 2 for photo-decomposition of aromatic dyes have also been explored. An attempt has been made to explore the plausible mechanism related with the decrease in fluorescence intensity of 1 and 2 in presence of NACs using theoretical calculations. Additionally, the probable mechanism of photo catalysis by 1 and 2 to photo-degrade aromatic dyes has been explained using density of states (DOS calculations.

  5. Photocatalytic degradation of textile azo dye over Ce{sub 1-x}Sn {sub x}O{sub 2} series

    Energy Technology Data Exchange (ETDEWEB)

    Borker, Pritam [Department of Chemistry, Goa University, Goa 403 206 (India); Salker, A.V. [Department of Chemistry, Goa University, Goa 403 206 (India)]. E-mail: sal_arun@rediffmail.com

    2006-08-25

    Ce{sub 1-x}Sn {sub x}O{sub 2} (x = 0, 0.1, 0.2, 0.3 and 1.0) have been prepared by co-precipitation method and characterized by XRD, FTIR, BET surface area and TG/DSC methods. The solid state studies such as electrical resistivity, magnetic susceptibility and diffuse reflectance measurements have been carried out and are attempted to correlate with the photocatalytic activity of these compositions. Solar radiation induced degradation of the textile diazo dye Naphthol Blue Black (NBB) has been carried out on these semiconductor compositions. The surface adsorbed oxygen plays an important role in scavenging photogenerated electrons thus preventing the recombination between electron and hole, inducing effective photodegradation.

  6. A Triphenylamine-Based Conjugated Polymer with Donor-π-Acceptor Architecture as Organic Sensitizer for Dye-Sensitized Solar Cells.

    Science.gov (United States)

    Zhang, Wei; Fang, Zhen; Su, Mingjuan; Saeys, Mark; Liu, Bin

    2009-09-17

    A conjugated polymer containing an electron donating backbone (triphenylamine) and an electron accepting side chain (cyanoacetic acid) with conjugated thiophene units as the linkers has been synthesized. Dye-sensitized solar cells (DSSCs) are fabricated utilizing this material as the dye sensitizer, resulting a typical power conversion efficiency of 3.39% under AM 1.5 G illumination, which represents the highest efficiency for polymer dye-sensitized DSSCs reported so far. The results show the good promise of conjugated polymers as sensitizers for DSSC applications. Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Assessment of molecularly imprinted polymers (MIPs) in the preconcentration of disperse red 73 dye prior to photoelectrocatalytic treatment.

    Science.gov (United States)

    Franco, Jefferson Honorio; Aissa, Alejandra Ben; Bessegato, Guilherme Garcia; Fajardo, Laura Martinez; Zanoni, Maria Valnice Boldrin; Pividori, María Isabel; Del Pilar Taboada Sotomayor, Maria

    2017-02-01

    Magnetic molecularly imprinted polymers (MMIPs) have become a research hotspot due to their two important characteristics: target recognition and magnetic separation. This paper presents the preparation, characterization, and optimization of an MMIP for the preconcentration of disperse red 73 dye (DR73) and its subsequent efficient degradation by photoelectrocatalytic treatment. The MMIPs were characterized by scanning electron microscopy (SEM), which revealed homogeneous distribution of the particles. Excellent encapsulation of magnetite was confirmed by transmission electron microscopy (TEM). A study of dye binding showed that the dye was retained more selectively in the MIP, compared to the NIP. The release of DR73 from the imprinted polymers into methanol and acetic acid was analyzed by UV-Vis spectrophotometry. The extracts showed higher absorbance values for MMIP, compared to MNIP, confirming greater adsorption of dye in the MMIP material. The extracts were then subjected to photoelectrocatalytic treatment. LC-MS/MS analysis following this treatment showed that the dye was almost completely degraded. Hence, the combination of MMIP extraction and photoelectrocatalysis offers an alternative way of selectively removing an organic contaminant, prior to proceeding with its complete degradation.

  8. Encapsulation of dye molecules into mesoporous polymer resin and mesoporous polymer-silica films by an evaporation-induced self-assembly method

    Energy Technology Data Exchange (ETDEWEB)

    Chi Yue; Li Nan; Tu Jinchun; Zhang Yujie [School of Material Science and Engineering, Key Laboratory of Automobile Materials of Ministry of Education, Jilin University, Changchun 130012 (China); Li Xiaotian, E-mail: xiaotianli@jlu.edu.c [School of Material Science and Engineering, Key Laboratory of Automobile Materials of Ministry of Education, Jilin University, Changchun 130012 (China); Shao Changlu, E-mail: clshao@nenu.edu.c [Center for Advanced Optoelectronic Functional Materials Research, Northeast Normal University, Changchun 130024 (China)

    2010-03-15

    Polymer resin and polymer-silica films with highly ordered mesostructure have been used as host materials to encapsulate DCM (4-(dicyanomethylene) -2-methyl-6-(4-dimethylaminostyryl)-4h-pyran), a kind of fluorescent dye, through evaporation-induced self-assembly method (EISA). After encapsulation, the composites show significant blue-shift in photoluminescence (PL) spectra. Particularly, by changing the excitation wavelength, the samples show different emission bands. These phenomena are related to the mesostructure and the positions of DCM molecules in the host.

  9. Phthaloylchitosan-Based Gel Polymer Electrolytes for Efficient Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    S. N. F. Yusuf

    2014-01-01

    Full Text Available Phthaloylchitosan-based gel polymer electrolytes were prepared with tetrapropylammonium iodide, Pr4NI, as the salt and optimized for conductivity. The electrolyte with the composition of 15.7 wt.% phthaloylchitosan, 31.7 wt.% ethylene carbonate (EC, 3.17 wt.% propylene carbonate (PC, 19.0 wt.% of Pr4NI, and 1.9 wt.% iodine exhibits the highest room temperature ionic conductivity of 5.27 × 10−3 S cm−1. The dye-sensitized solar cell (DSSC fabricated with this electrolyte exhibits an efficiency of 3.5% with JSC of 7.38 mA cm−2, VOC of 0.72 V, and fill factor of 0.66. When various amounts of lithium iodide (LiI were added to the optimized gel electrolyte, the overall conductivity is observed to decrease. However, the efficiency of the DSSC increases to a maximum value of 3.71% when salt ratio of Pr4NI : LiI is 2 : 1. This cell has JSC, VOC and fill factor of 7.25 mA cm−2, 0.77 V and 0.67, respectively.

  10. Fullerene-catalyzed reduction of azo derivatives in water under UV irradiation

    KAUST Repository

    Guo, Yong; Li, Wengang; Yan, Jingjing; Moosa, Basem; Amad, Maan H.; Werth, Charles; Khashab, Niveen M.

    2012-01-01

    Metal-free fullerene (C60) was found to be an effective catalyst for the reduction of azo groups in basic aqueous solution under UV irradiation in the presence of NaBH4. Use of NaBH4 by itself is not sufficient to reduce the azo dyes without the assistance of a metal catalyst such as Pd and Ag. Experimental and theoretical results suggest that C 60 catalyzes this reaction by using its vacant orbital to accept the electron in the bonding orbital of azo dyes, which leads to the activation of the N=N bond. UV irradiation increases the ability of C60 to interact with electron-donor moieties in azo dyes. Filling a vacancy: Experimental and theoretical methods have been combined to show that C60-catalyzed reductions of azo compounds form aromatic amines under UV irradiation (see scheme). The obtained results show that C60 acts as an electron acceptor to catalyze the reduction of azo compounds, and the role of UV irradiation is to increase the ability of C60 to interact with electron-donor moieties in azo compounds. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Fullerene-catalyzed reduction of azo derivatives in water under UV irradiation

    KAUST Repository

    Guo, Yong

    2012-09-27

    Metal-free fullerene (C60) was found to be an effective catalyst for the reduction of azo groups in basic aqueous solution under UV irradiation in the presence of NaBH4. Use of NaBH4 by itself is not sufficient to reduce the azo dyes without the assistance of a metal catalyst such as Pd and Ag. Experimental and theoretical results suggest that C 60 catalyzes this reaction by using its vacant orbital to accept the electron in the bonding orbital of azo dyes, which leads to the activation of the N=N bond. UV irradiation increases the ability of C60 to interact with electron-donor moieties in azo dyes. Filling a vacancy: Experimental and theoretical methods have been combined to show that C60-catalyzed reductions of azo compounds form aromatic amines under UV irradiation (see scheme). The obtained results show that C60 acts as an electron acceptor to catalyze the reduction of azo compounds, and the role of UV irradiation is to increase the ability of C60 to interact with electron-donor moieties in azo compounds. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Quaternized triethanolamine-sebacoyl moieties in highly branched polymer architecture as a host for the entrapment of acid dyes in aqueous solutions

    Directory of Open Access Journals (Sweden)

    Meriem Bendjelloul

    2017-03-01

    Full Text Available This paper reports the synthesis of a hyperbranched polymer by a cost-effective one-step copolymerization of A3 and B2 monomers, namely, triethanolamine and sebacoyl chloride, respectively, followed by methylation of tertiary amine groups. The structure of the hyperbranched polymer QTEAS as an efficient material for the removal of acid dyes was demonstrated by Fourier transform infrared spectroscopy (FTIR, cross polarization magic angle spinning (CPMAS 13C NMR, thermogravimetric analysis (TGA, powder X-ray diffraction (DRX and scanning electron microscopy (SEM. The removal of indigo carmine (IC and Evans blue (EB was expected to be driven by the electrostatic attraction between positively charged quaternary ammonium groups within the hyperbranched polymer and the negatively charged dyes. The removal process was found to be closely connected to the total number of sulfonate groups on the surface of the dyes. Nonetheless, the ionic strength does not affect the dyes' removal efficiency by the hyperbranched polymer. The sorption capacities at saturation of the monolayer qmax were determined to be 213.22 mg g−1 and 214.13 mg g−1, for IC and EB, respectively, thus showing the greater affinity of QTEAS sorbent for both dyes. Despite its extended molecular structure, EB is removed with the same effectiveness as IC. Finally, the great efficiency of the highly branched polymer for dye removal from colored wastewater was clearly demonstrated.

  13. The Hydractinia echinata Test-System. III: Structure-Toxicity Relationship Study of Some Azo-, Azo-Anilide, and Diazonium Salt Derivatives

    Directory of Open Access Journals (Sweden)

    Sergiu Adrian Chicu

    2014-07-01

    Full Text Available Structure-toxicity relationships for a series of 75 azo and azo-anilide dyes and five diazonium salts were developed using Hydractinia echinata (H. echinata as model species. In addition, based on these relationships, predictions for 58 other azo-dyes were made. The experimental results showed that the measured effectiveness Mlog(1/MRC50 does not depend on the number of azo groups or the ones corresponding to metobolites, but it is influenced by the number of anilide groups, as well as by the substituents’ positions within molecules. The conformational analysis pointed out the intramolecular hydrogen bonds, especially the simple tautomerization of quinoidic (STOH or aminoidic (STNH2 type. The effectiveness is strongly influenced by the “push-pull” electronic effect, specific to two hydroxy or amino groups separated by an azo moiety (double alternate tautomery, (DAT, to the –COOH or –SO3H groups which are located in ortho or para position with respect to the azo group. The levels of the lipophylic/hydrophilic, electronic and steric equilibriums, pointed out by the Mlog(1/MRC50 values, enabled the calculation of their average values Clog(1/MRC50 (“Köln model”, characteristic to one derivative class (class isotoxicity. The azo group reduction and the hydrolysis of the amido/peptidic group are two concurrent enzymatic reactions, which occur with different reaction rates and mechanisms. The products of the partial biodegradation are aromatic amines. No additive or synergic effects are noticed among them.

  14. Synthesis, Characterization and Photoinduction of Optical Anisotropy in Liquid Crystalline Diblock Azo-Copolymers

    DEFF Research Database (Denmark)

    Forcén, P; Oriol, L; Sánchez, C

    2007-01-01

    Diblock copolymers with polymethyl methacrylate and side chain liquid crystalline WC) azopolymethacrylate blocks were synthesized by atom transfer radical polymerization (ATRP). The azobeazene content in these copolymers ranges from 52 to 7 wt %. For an azo conteat dowri to 20% they exhibit a LC...... anisotropy induced in these films by illumination with linearly polarized 488 nm light was studied and the resuits compared with those of the azo homopolymer and of a random copolymer with a similar composition. The formation of azo aggregates inside the azo blocks is strongly reduced in going from...... the homopolymer to the copolymers. Photoinduced azo orientation perpendicular to the 488 nm light polarization was found in aH the polymers. The orientational order parameter is very similar in the homopolymer and in the block copolymers with an azo content down to 20 wt %, while it is much lower in the random...

  15. Mycoremediation of congo red dye by filamentous fungi

    OpenAIRE

    Bhattacharya, Sourav; Das, Arijit; G, Mangai.; K, Vignesh.; J, Sangeetha.

    2011-01-01

    Azo, anthroquinone and triphenylmethane dyes are the major classes of synthetic colourants, which are difficult to degrade and have received considerable attention. Congo red, a diazo dye, is considered as a xenobiotic compound, and is recalcitrant to biodegradative processes. Nevertheless, during the last few years it has been demonstrated that several fungi, under certain environmental conditions, are able to transfer azo dyes to non toxic products using laccases. The aim of this work was t...

  16. The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors

    OpenAIRE

    Faith M. Akwi; Paul Watts

    2016-01-01

    Summary In this paper, a micro-fluidic optimized process for the continuous flow synthesis of azo compounds is presented. The continuous flow synthesis of Sudan II azo dye was used as a model reaction for the study. At found optimal azo coupling reaction temperature and pH an investigation of the optimum flow rates of the reactants for the diazotization and azo coupling reactions in Little Things Factory-MS microreactors was performed. A conversion of 98% was achieved in approximately 2.4 min...

  17. Preparation of lysine-decorated polymer-brush-grafted magnetic nanocomposite for the efficient and selective adsorption of organic dye

    Science.gov (United States)

    Jing, Shiyao; Wang, Xin; Tan, Yebang

    2018-05-01

    A novel magnetic nanocomposite (Lys-PGMA@Fe3O4) containing amphoteric polymer brushes was synthesized by combining surface-initiated atom-transfer radical polymerization and lysine modification. The chemical structure of Lys-PGMA@Fe3O4 was confirmed by multiple methods, such as FT-IR, TGA, elemental analysis. The core-brush morphology was clearly observed by transmission electron microscopy. Lys-PGMA@Fe3O4 was then used to selectively and efficiently adsorb hazardous dyes. Adsorption results showed that Lys-PGMA@Fe3O4 had considerable adsorption capacity (0.54 and 0.85 mmol·g-1 for LY and MEB, respectively) and rapid adsorption rate (within 10 min), which can be attributed to the nanosize and abundant adsorptive polymer brushes. The selective adsorption of a mixture of lemon yellow (pH = 4.0) and methylene blue (pH = 10.0) was achieved through the amphoteric polymer brushes. Similar to traditional adsorbent materials, Lys-PGMA@Fe3O4 also showed easy magnet-assisted separation property. Lys-PGMA@Fe3O4 adsorbent can also be regenerated to reduce application cost. Overall, results demonstrated that Lys-PGMA@Fe3O4 nanocomposite was an excellent adsorbent material for removing dye pollutants from wastewater.

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

    Energy Technology Data Exchange (ETDEWEB)

    Sreedhar, Sreeja, E-mail: sreejasreedhar83@gmail.com; Muneera, C. I., E-mail: drcimuneera@hotmail.com [Department of Physics, University of Kerala, Kariavattom, Thiruvananthapuram 695581, Kerala (India); Illyaskutty, Navas [Institute for Sensorics and Information Systems (ISIS), Karlsruhe University of Applied Sciences, Moltkestr. 30, D-76133 Karlsruhe (Germany); Sreedhanya, S. [School of Chemical Sciences, M. G. University, Kottayam, Kerala 686560 (India); Philip, Reji [Light and Matter Physics Group, Raman Research Institute, Bangalore 560080 (India)

    2016-05-21

    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.

  19. Present status of solid state photoelectrochemical solar cells and dye sensitized solar cells using PEO-based polymer electrolytes

    International Nuclear Information System (INIS)

    Singh, Pramod Kumar; Bhattacharya, Bhaskar; Nagarale, R K; Pandey, S P; Rhee, H W

    2011-01-01

    Due to energy crises in the future, much effort is being directed towards alternate sources. Solar energy is accepted as a novel substitute for conventional sources of energy. Out of the long list of various types of solar cells available on the market, solid state photoelectrochemical solar cells (SSPECs) and dye sensitized solar cells (DSSCs) are proposed as an alternative to costly crystalline solar cell. This review provides a common platform for SSPECs and DSSCs using polymer electrolyte, particularly on polyethylene oxide (PEO)-based polymer electrolytes. Due to numerous advantageous properties of PEO, it is frequently used as an electrolyte in both SSPECs as well as DSSCs. In DSSCs, so far high efficiency (more than 11%) has been obtained only by using volatile liquid electrolyte, which suffers many disadvantages, such as corrosion, leakage and evaporation. The PEO-based solid polymer proves its importance and could be used to solve the problems stated above. The recent developments in SSPECs and DSSCs using modified PEO electrolytes by adding nano size inorganic fillers, blending with low molecular weight polymers and ionic liquid (IL) are discussed in detail. The role of ionic liquid in modifying the electrical, structural and photoelectrochemical properties of PEO polymer electrolytes is also described. (review)

  20. Present status of solid state photoelectrochemical solar cells and dye sensitized solar cells using PEO-based polymer electrolytes

    Science.gov (United States)

    Singh, Pramod Kumar; Nagarale, R. K.; Pandey, S. P.; Rhee, H. W.; Bhattacharya, Bhaskar

    2011-06-01

    Due to energy crises in the future, much effort is being directed towards alternate sources. Solar energy is accepted as a novel substitute for conventional sources of energy. Out of the long list of various types of solar cells available on the market, solid state photoelectrochemical solar cells (SSPECs) and dye sensitized solar cells (DSSCs) are proposed as an alternative to costly crystalline solar cell. This review provides a common platform for SSPECs and DSSCs using polymer electrolyte, particularly on polyethylene oxide (PEO)-based polymer electrolytes. Due to numerous advantageous properties of PEO, it is frequently used as an electrolyte in both SSPECs as well as DSSCs. In DSSCs, so far high efficiency (more than 11%) has been obtained only by using volatile liquid electrolyte, which suffers many disadvantages, such as corrosion, leakage and evaporation. The PEO-based solid polymer proves its importance and could be used to solve the problems stated above. The recent developments in SSPECs and DSSCs using modified PEO electrolytes by adding nano size inorganic fillers, blending with low molecular weight polymers and ionic liquid (IL) are discussed in detail. The role of ionic liquid in modifying the electrical, structural and photoelectrochemical properties of PEO polymer electrolytes is also described.

  1. Influence of solvent on the poly (acrylic acid)-oligo-(ethylene glycol) polymer gel electrolyte and the performance of quasi-solid-state dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Wu, Jihuai; Lan, Zhang; Lin, Jianming; Huang, Miaoliang; Hao, Shancun; Fang, Leqing

    2007-01-01

    The influence of solvents on the property of poly (acrylic acid)-oligo-(ethylene glycol) polymer gel electrolyte and photovoltaic performance of quasi-solid-state dye-sensitized solar cells (DSSCs) were investigated. Solvents or mixed solvents with large donor number enhance the liquid electrolyte absorbency, which further influences the ionic conductivity of polymer gel electrolyte. A polymer gel electrolyte with ionic conductivity of 4.45 mS cm -1 was obtained by using poly (acrylic acid)-oligo-(ethylene glycol) as polymer matrix, and absorbing 30 vol.% N-methyl pyrrolidone and 70 vol.% γ-butyrolactone with 0.5 M NaI and 0.05 M I 2 . By using this polymer gel electrolyte coupling with 0.4 M pyridine additive, a quasi-solid-state dye-sensitized solar cell with conversion efficiency of 4.74% was obtained under irradiation of 100 mW cm -2 (AM 1.5)

  2. Reversible light-controlled conductance switching of azobenzene-based metal/polymer nanocomposites

    International Nuclear Information System (INIS)

    Pakula, Christina; Zaporojtchenko, Vladimir; Strunskus, Thomas; Faupel, Franz; Zargarani, Dordaneh; Herges, Rainer

    2010-01-01

    We present a new concept of light-controlled conductance switching based on metal/polymer nanocomposites with dissolved chromophores that do not have intrinsic current switching ability. Photoswitchable metal/PMMA nanocomposites were prepared by physical vapor deposition of Au and Pt clusters, respectively, onto spin-coated thin poly(methylmethacrylate) films doped with azo-dye molecules. High dye concentrations were achieved by functionalizing the azo groups with tails and branches, thus enhancing solubility. The composites show completely reversible optical switching of the absorption bands upon alternating irradiation with UV and blue light. We also demonstrate reversible light-controlled conductance switching. This is attributed to changes in the metal cluster separation upon isomerization based on model experiments where analogous conductance changes were induced by swelling of the composite films in organic vapors and by tensile stress.

  3. The effect of dioctyl sodium sulphosuccinate on tartrazine azo reduction by intestinal bacteria.

    Science.gov (United States)

    Allan, R J; Roxon, J J

    1977-03-01

    1. Washed whole-cell suspensions of Proteus vulgaris and micro-organisms from rat faeces, reductively cleave the azo bond of the food dye tartrazine under anaerobic conditions. 2. Dioctyl sodium sulphosuccinate, a common faecal softening laxative, when added to incubations in vitro at concentrations greater than 0.005%, increases tartrazine azo reduction in P. vulgaris whole-cell suspensions. 3. By contrast, concentrations of dioctyl sodium sulphosuccinate greater than 0.005% when added to incubations in vitro of rat faecal preparations, resulted in an inhibition of tartrazine azo reduction.

  4. The use of poly(vinylpyridine-co-acrylonitrile) in polymer electrolytes for quasi-solid dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Li, Minyu; Feng, Shujing; Fang, Shibi; Xiao, Xurui; Li, Xueping; Zhou, Xiaowen; Lin, Yuan

    2007-01-01

    Poly(vinylpyridine-co-acrylonitrile) (P(VP-co-AN)) was used to form polymer electrolytes for dye-sensitized solar cells (DSSCs). The effects of P(VP-co-AN) on the photovoltaic performances of DSSCs have been investigated with nonaqueous electrolytes containing alkali-iodide and iodine. It was found that the effect of P(VP-co-AN) on V oc closely related to its amount in the electrolyte. Lower amount of P(VP-co-AN) was benefit for the construction of a solar cell containing P(VP-co-AN) with higher energy conversion efficiency. Chemically crosslinking solidification with backbone polymer P(VP-co-AN) amount of 3% fabricated quasi-solid DSSCs with 10% increased conversion efficiencies with relative to that of the initial liquid DSSCs

  5. Scattering-layer-induced energy storage function in polymer-based quasi-solid-state dye-sensitized solar cells.

    Science.gov (United States)

    Zhang, Xi; Jiang, Hongrui

    2015-03-09

    Photo-self-charging cells (PSCs) are compact devices with dual functions of photoelectric conversion and energy storage. By introducing a scattering layer in polymer-based quasi-solid-state dye-sensitized solar cells, two-electrode PSCs with highly compact structure were obtained. The charge storage function stems from the formed ion channel network in the scattering layer/polymer electrolyte system. Both the photoelectric conversion and the energy storage functions are integrated in only the photoelectrode of such PSCs. This design of PSC could continuously output power as a solar cell with considerable efficiency after being photo-charged. Such PSCs could be applied in highly-compact mini power devices.

  6. Azo biphenyl polyurethane: Preparation, characterization and application for optical waveguide switch

    Science.gov (United States)

    Jiang, Yan; Da, Zulin; Qiu, Fengxian; Yang, Dongya; Guan, Yijun; Cao, Guorong

    2018-01-01

    Azo waveguide polymers are of particular interest in the design of materials for applications in optical switch. The aim of this contribution was the synthesis and thermo-optic waveguide switch properties of azo biphenyl polyurethanes. A series of monomers and azo biphenyl polyurethanes (Azo BPU1 and Azo BPU2) were synthesized and characterized by FT-IR, UV-Vis spectroscopy and 1H NMR. The physical and mechanical properties of thin polymer films were measured. The refractive index and thermo-optic coefficient (dn/dT) of polymer films were investigated for TE (transversal electric) polarizations by ATR technique. The transmission loss of film was measured using the Charge Coupled Device digital imaging devices. The results showed the Azo BPU2 containing chiral azobenzene chromophore had higher dn/dT and lower transmission loss. Subsequently, a 1 × 2 Y-branch and 2 × 2 Mach-Zehnder optical switches based on the prepared polymers were designed and simulated. The results showed that the power consumption of all switches was less than 1.0 mW. Compared with 1 × 2 Y-branch optical switch, the 2 × 2 Mach-Zehnder optical switches based on the same polymer have the faster response time, which were about only 1.2 and 2.0 ms, respectively.

  7. Removal of hazardous dye Ponceau-S by using Chitin:

    African Journals Online (AJOL)

    Sr030111Bin Comp

    Key words: Chitin, Ponceau-S, organic bioadsorbent, colored organic, industrial effluents. ..... of cationic azo dye by TiO2/bentonite nanocomposite, J. Photochem. ... effluents to freshwater and estuarine algae, crustaceans and fishes. Environ.

  8. Sorption isotherms, kinetic and optimization process of amino acid proline based polymer nanocomposite for the removal of selected textile dyes from industrial wastewater.

    Science.gov (United States)

    Raghunath, Sharista; Anand, K; Gengan, R M; Nayunigari, Mithil Kumar; Maity, Arjun

    2016-12-01

    In this article, adsorption and kinetic studies were carried out on three textile dyes, namely Reactive Blue 222 (RB 222), Reactive Red 195 (RR 195) and Reactive Yellow 145 (RY 145). The dyes studied in a mixture were adsorbed under various conditions onto PRO-BEN, a bentonite modified with a new cationic proline polymer (l-proline-epichlorohydrin polymer). The proline polymer was characterized by 1 H NMR, Fourier transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS) and TEM. The PRO-BEN composite was characterized by FT-IR, dynamic light scattering (DLS) (zeta potential), TEM imaging, SEM/EDX and X-ray photoelectron spectroscopy (characterize the binding energy). During adsorption studies, factors involving pH, temperature, the initial concentrations of the dyes and the quantity of PRO-BEN used during adsorption were established. The results revealed that the adsorption mechanism was categorized by the Langmuir type 1 isotherm. The adsorption data followed the pseudo-second order kinetic model. The intraparticle diffusion model indicated that adsorption did not only depend on the intraparticle diffusion of the dyes. The thermodynamic parameters verified that the adsorption process was spontaneous and exothermic. The Gibbs free energy values indicated that physisorption had occurred. Successful adsorption of dyes from an industrial effluent was achieved. Desorption studies concluded that PRO-BEN desorbed the dyes better than alumina. This can thereby be viewed as a recyclable remediation material. The PRO-BEN composite could be a cost efficient alternative towards the removal of organic dyes in wastewater treatment. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. Newer approach of using alternatives to (Indium doped) metal electrodes, dyes and electrolytes in dye sensitized solar cell

    Science.gov (United States)

    Patni, Neha; Sharma, Pranjal; Pillai, Shibu G.

    2018-04-01

    This work demonstrates the PV study of dye sensitised solar cells by fabricating the (PV) cell using the ITO, FTO and AZO glass substrate. Dyes used for the fabrication were extracted from beetroot and spinach and a cocktail dye by mixing both of the dyes was also prepared. Similarly the three dufferent electrolytes used were iodide-triiodide couple, polyaniline and mixture of polyaniline and iodide couple. Mixed dye and mixed electrolyte has emerged as the highest efficient cell. The electrical characterisation shows that the highest power conversion efficiency of 1.86% was achieved by FTO substrate, followed by efficiency of 1.83% by AZO substrate and efficiency of 1.63% with ITO substrate using mixed dye and mixed electrolyte approach. This justifies that FTO and AZO shows better efficiency and hence proposed to be used as an alternative to indium free system.

  10. Dye-based coatings for hydrophobic valves and their application to polymer labs-on-a-chip

    Science.gov (United States)

    Riegger, L.; Mielnik, M. M.; Gulliksen, A.; Mark, D.; Steigert, J.; Lutz, S.; Clad, M.; Zengerle, R.; Koltay, P.; Hoffmann, J.

    2010-04-01

    We provide a method for the selective surface patterning of microfluidic chips with hydrophobic fluoropolymers which is demonstrated by the fabrication of hydrophobic valves via dispensing. It enables efficient optical quality control for the surface patterning thus permitting the low-cost production of highly reproducible hydrophobic valves. Specifically, different dyes for fluoropolymers enabling visual quality control (QC) are investigated, and two fluoropolymer-solvent-dye solutions based on fluorescent quantum dots (QD) and carbon black (CB) are presented in detail. The latter creates superhydrophobic surfaces on arbitrary substrates, e.g. chips made from cyclic olefin copolymer (COC, water contact angle = 157.9°), provides good visibility for the visual QC in polymer labs-on-a-chip and increases the burst pressures of the hydrophobic valves. Finally, an application is presented which aims at the on-chip amplification of mRNA based on defined flow control by hydrophobic valves is presented. Here, the optimization based on QC in combination with the Teflon-CB coating improves the burst pressure reproducibility from 14.5% down to 6.1% compared to Teflon-coated valves.

  11. The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors.

    Science.gov (United States)

    Akwi, Faith M; Watts, Paul

    2016-01-01

    In this paper, a micro-fluidic optimized process for the continuous flow synthesis of azo compounds is presented. The continuous flow synthesis of Sudan II azo dye was used as a model reaction for the study. At found optimal azo coupling reaction temperature and pH an investigation of the optimum flow rates of the reactants for the diazotization and azo coupling reactions in Little Things Factory-MS microreactors was performed. A conversion of 98% was achieved in approximately 2.4 minutes and a small library of azo compounds was thus generated under these reaction conditions from couplers with aminated or hydroxylated aromatic systems. The scaled up synthesis of these compounds in PTFE tubing (i.d. 1.5 mm) was also investigated, where good reaction conversions ranging between 66-91% were attained.

  12. The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors

    Directory of Open Access Journals (Sweden)

    Faith M. Akwi

    2016-09-01

    Full Text Available In this paper, a micro-fluidic optimized process for the continuous flow synthesis of azo compounds is presented. The continuous flow synthesis of Sudan II azo dye was used as a model reaction for the study. At found optimal azo coupling reaction temperature and pH an investigation of the optimum flow rates of the reactants for the diazotization and azo coupling reactions in Little Things Factory-MS microreactors was performed. A conversion of 98% was achieved in approximately 2.4 minutes and a small library of azo compounds was thus generated under these reaction conditions from couplers with aminated or hydroxylated aromatic systems. The scaled up synthesis of these compounds in PTFE tubing (i.d. 1.5 mm was also investigated, where good reaction conversions ranging between 66–91% were attained.

  13. Improvement of N-phthaloylchitosan based gel polymer electrolyte in dye-sensitized solar cells using a binary salt system.

    Science.gov (United States)

    Yusuf, S N F; Azzahari, A D; Selvanathan, V; Yahya, R; Careem, M A; Arof, A K

    2017-02-10

    A binary salt system utilizing lithium iodide (LiI) as the auxiliary component has been introduced to the N-phthaloylchitosan (PhCh) based gel polymer electrolyte consisting of ethylene carbonate (EC), dimethylformamide (DMF), tetrapropylammonium iodide (TPAI), and iodine (I 2 ) in order to improve the performance of dye-sensitized solar cell (DSSC) with efficiency of 6.36%, photocurrent density, J SC of 17.29mAcm -2 , open circuit voltage, V OC of 0.59V and fill factor, FF of 0.62. This efficiency value is an improvement from the 5.00% performance obtained by the DSSC consisting of only TPAI single salt system. The presence of the LiI in addition to the TPAI improves the charge injection rates and increases the iodide contribution to the total conductivity and both factors contribute to the increase in efficiency of the DSSC. The interaction behavior between polymer-plasticizer-salt was thoroughly investigated using EIS, FTIR spectroscopy and XRD. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Computational models for structure-hydrophobicity relationships of 4-carboxyl-2,6-dinitrophenyl azo hydroxynaphthalenes.

    Science.gov (United States)

    Idowu, Olakunle S; Adegoke, Olajire A; Idowu, Abiola; Olaniyi, Ajibola A

    2007-01-01

    Some phenyl azo hydroxynaphthalene dyes (e.g., sunset yellow) are certified as approved colorants for food, cosmetics, and drug formulations. The hydrophobicity of 4 newly synthesized azo dyes of the phenyl azo hydroxynaphthalene class was investigated, as a training set, with the goal of developing models for quantitative structure-property relationships (QSPR). Retention behavior of the molecules reversed-phase thin-layer chromatography (RPTLC) was investigated using liquid paraffin-coated silica gel as the stationary phase. Mobile phases consisted of aqueous mixtures of methanol, acetone, and dimethylformamide (DMF). Basic hydrophobicity parameter (Rmw), specific hydrophobic surface area (S), and isocratic chromatographic hydrophobicity index (phio) were computed from the chromatographic data. The hydrophobicity index (Rm) decreased linearly with increasing concentration of organic modifiers. Extrapolated Rmw values obtained by using DMF and acetone differ significantly from the value obtained by using methanol as organic modifier [P dyes and may also play useful roles in computer-assisted molecular discovery of nontoxic azo dyes.

  15. Gold nanoworms immobilized graphene oxide polymer brush nanohybrid for catalytic degradation studies of organic dyes

    International Nuclear Information System (INIS)

    Mogha, Navin Kumar; Gosain, Saransh; Masram, Dhanraj T.

    2017-01-01

    Highlights: • AuNPs on PDMAEMA brushes immobilized reduced graphene oxide was used as catalyst. • A novel highly efficient, reusable heterogeneous catalyst for dyes degradation. • Rhodamine B, Methyl Orange and Eosin Y was used for study. • Apparent rate constant observed was 21.8, 26.2, and 8.7 (×10 −3 s −1 ) respectively. - Abstract: In the present work, we report gold nanoparticles (AuNPs) on poly (dimethylaminoethyl methacrylate) (PDMAEMA) brushes immobilized reduced graphene oxide (Au/PDMAEMA/RGO) as catalyst for degradation kinetic studies of Rhodamine B (RB), Methyl Orange (MO) and Eosine Y (EY) dyes, having an excellent catalytic activity, as evident by the apparent rate constant (k app ), which is found to be 21.8, 26.2, and 8.7 (×10 −3 s −1 ), for RB, MO and EY respectively. Au/PDMAEMA/RGO catalyst is easy to use, highly efficient, recyclable, which make it suitable for applications in waste water management. Foremost, synthesis of PDMAEMA brushes on graphene oxide is accomplished by Atom transfer radical polymerization method (ATRP), whereas AuNPs are synthesized by simple chemical reduction method.

  16. Gold nanoworms immobilized graphene oxide polymer brush nanohybrid for catalytic degradation studies of organic dyes

    Energy Technology Data Exchange (ETDEWEB)

    Mogha, Navin Kumar; Gosain, Saransh; Masram, Dhanraj T., E-mail: dhnaraj_masram27@rediffmail.com

    2017-02-28

    Highlights: • AuNPs on PDMAEMA brushes immobilized reduced graphene oxide was used as catalyst. • A novel highly efficient, reusable heterogeneous catalyst for dyes degradation. • Rhodamine B, Methyl Orange and Eosin Y was used for study. • Apparent rate constant observed was 21.8, 26.2, and 8.7 (×10{sup −3} s{sup −1}) respectively. - Abstract: In the present work, we report gold nanoparticles (AuNPs) on poly (dimethylaminoethyl methacrylate) (PDMAEMA) brushes immobilized reduced graphene oxide (Au/PDMAEMA/RGO) as catalyst for degradation kinetic studies of Rhodamine B (RB), Methyl Orange (MO) and Eosine Y (EY) dyes, having an excellent catalytic activity, as evident by the apparent rate constant (k{sub app}), which is found to be 21.8, 26.2, and 8.7 (×10{sup −3} s{sup −1}), for RB, MO and EY respectively. Au/PDMAEMA/RGO catalyst is easy to use, highly efficient, recyclable, which make it suitable for applications in waste water management. Foremost, synthesis of PDMAEMA brushes on graphene oxide is accomplished by Atom transfer radical polymerization method (ATRP), whereas AuNPs are synthesized by simple chemical reduction method.

  17. Gold nanoworms immobilized graphene oxide polymer brush nanohybrid for catalytic degradation studies of organic dyes

    Science.gov (United States)

    Mogha, Navin Kumar; Gosain, Saransh; Masram, Dhanraj T.

    2017-02-01

    In the present work, we report gold nanoparticles (AuNPs) on poly (dimethylaminoethyl methacrylate) (PDMAEMA) brushes immobilized reduced graphene oxide (Au/PDMAEMA/RGO) as catalyst for degradation kinetic studies of Rhodamine B (RB), Methyl Orange (MO) and Eosine Y (EY) dyes, having an excellent catalytic activity, as evident by the apparent rate constant (kapp), which is found to be 21.8, 26.2, and 8.7 (×10-3 s-1), for RB, MO and EY respectively. Au/PDMAEMA/RGO catalyst is easy to use, highly efficient, recyclable, which make it suitable for applications in waste water management. Foremost, synthesis of PDMAEMA brushes on graphene oxide is accomplished by Atom transfer radical polymerization method (ATRP), whereas AuNPs are synthesized by simple chemical reduction method.

  18. Surface grafting of zwitterionic polymers onto dye doped AIE-active luminescent silica nanoparticles through surface-initiated ATRP for biological imaging applications

    Science.gov (United States)

    Mao, Liucheng; Liu, Xinhua; Liu, Meiying; Huang, Long; Xu, Dazhuang; Jiang, Ruming; Huang, Qiang; Wen, Yuanqing; Zhang, Xiaoyong; Wei, Yen

    2017-10-01

    Aggregation-induced emission (AIE) dyes have recently been intensively explored for biological imaging applications owing to their outstanding optical feature as compared with conventional organic dyes. The AIE-active luminescent silica nanoparticles (LSNPs) are expected to combine the advantages both of silica nanoparticles and AIE-active dyes. Although the AIE-active LSNPs have been prepared previously, surface modification of these AIE-active LSNPs with functional polymers has not been reported thus far. In this work, we reported a rather facile and general strategy for preparation of polymers functionalized AIE-active LSNPs through the surface-initiated atom transfer radical polymerization (ATRP). The AIE-active LSNPs were fabricated via direct encapsulation of AIE-active dye into silica nanoparticles through a non-covalent modified Stöber method. The ATRP initiator was subsequently immobilized onto these AIE-active LSNPs through amidation reaction between 3-aminopropyl-triethoxy-silane and 2-bromoisobutyryl bromide. Finally, the zwitterionic 2-(methacryloyloxy)ethyl phosphorylcholine (MPC) was selected as model monomer and grafted onto MSNs through ATRP. The characterization results suggested that LSNPs can be successfully modified with poly(MPC) through surface-initiated ATRP. The biological evaluation results demonstrated that the final SNPs-AIE-pMPC composites possess low cytotoxicity, desirable optical properties and great potential for biological imaging. Taken together, we demonstrated that AIE-active LSNPs can be fabricated and surface modified with functional polymers to endow novel functions and better performance for biomedical applications. More importantly, this strategy developed in this work could also be extended for fabrication of many other LSNPs polymer composites owing to the good monomer adoptability of ATRP.

  19. Determinação de corantes marcadores do tipo azo e antraquinona em combustíveis por cromatografia líquida com detecção eletroquímica Determination of azo and anthraquinone dyes in fuels sample using hplc with electrochemical detection

    Directory of Open Access Journals (Sweden)

    Magno Aparecido Gonçalves Trindade

    2010-01-01

    Full Text Available An analytical method based on high-performance liquid chromatography with electrochemical detection has been developed and applied to the determination of Solvent blue 14 (SA-14 and Solvent red 24 (SV-24 in fuel samples. The dyes were better separated on C18 column, using a mobile phase composed of acetonitrile and ammonium acetate (90:10, v/v. Detection was carried out at an oxidation potential of +0.85V. The detector response was linear at concentration range of 7.50×10-8 - 1.50×10-6 mol L-1 (r = 0.997 for SA-14 and SV-24, respectively. The method was used to quantify these dyes in fuels samples with satisfactory accuracy and precision.

  20. Microbial fuel cell operation using monoazo and diazo dyes as terminal electron acceptor for simultaneous decolourisation and bioelectricity generation.

    Science.gov (United States)

    Oon, Yoong-Sin; Ong, Soon-An; Ho, Li-Ngee; Wong, Yee-Shian; Oon, Yoong-Ling; Lehl, Harvinder Kaur; Thung, Wei-Eng; Nordin, Noradiba

    2017-03-05

    Monoazo and diazo dyes [New coccine (NC), Acid orange 7 (AO7), Reactive red 120 (RR120) and Reactive green 19 (RG19)] were employed as electron acceptors in the abiotic cathode of microbial fuel cell. The electrons and protons generated from microbial organic oxidation at the anode which were utilized for electrochemical azo dye reduction at the cathodic chamber was successfully demonstrated. When NC was employed as the electron acceptor, the chemical oxygen demand (COD) removal and dye decolourisation efficiencies obtained at the anodic and cathodic chamber were 73±3% and 95.1±1.1%, respectively. This study demonstrated that the decolourisation rates of monoazo dyes were ∼50% higher than diazo dyes. The maximum power density in relation to NC decolourisation was 20.64mW/m 2 , corresponding to current density of 120.24mA/m 2 . The decolourisation rate and power output of different azo dyes were in the order of NC>AO7>RR120>RG19. The findings revealed that the structure of dye influenced the decolourisation and power performance of MFC. Azo dye with electron-withdrawing group at para substituent to azo bond would draw electrons from azo bond; hence the azo dye became more electrophilic and more favourable for dye reduction. Copyright © 2016 Elsevier B.V. All rights reserved.

  1. Statistical optimization and artificial neural network modeling for acridine orange dye degradation using in-situ synthesized polymer capped ZnO nanoparticles.

    Science.gov (United States)

    Dhiman, Nitesh; Markandeya; Singh, Amrita; Verma, Neeraj K; Ajaria, Nidhi; Patnaik, Satyakam

    2017-05-01

    ZnO NPs were synthesized by a prudent green chemistry approach in presence of polyacrylamide grafted guar gum polymer (pAAm-g-GG) to ensure uniform morphology, and functionality and appraised for their ability to degrade photocatalytically Acridine Orange (AO) dye. These ZnO@pAAm-g-GG NPs were thoroughly characterized by various spectroscopic, XRD and electron microscopic techniques. The relative quantity of ZnO NPs in polymeric matrix has been estimated by spectro-analytical procedure; AAS and TGA analysis. The impact of process parameters viz. NP's dose, contact time and AO dye concentration on percentage photocatalytic degradation of AO dyes were evaluated using multivariate optimizing tools, Response Surface Methodology (RSM) involving Box-Behnken Design (BBD) and Artificial Neural Network (ANN). Congruity of the BBD statistical model was implied by R 2 value 0.9786 and F-value 35.48. At RSM predicted optimal condition viz. ZnO@pAAm-g-GG NP's dose of 0.2g/L, contact time of 210min and AO dye concentration 10mg/L, a maximum of 98% dye degradation was obtained. ANOVA indicated appropriateness of the model for dye degradation owing to "Prob.>F" less than 0.05 for variable parameters. We further, employed three layers feed forward ANN model for validating the BBD process parameters and suitability of our chosen model. The evaluation of Levenberg-Marquardt algorithm (ANN1) and Gradient Descent with adaptive learning rate (ANN2) model employed to scrutinize the best method and found experimental values of AO dye degradation were in close to those with predicated value of ANN 2 modeling with minimum error. Copyright © 2017 Elsevier Inc. All rights reserved.

  2. High-Quality AZO/Au/AZO Sandwich Film with Ultralow Optical Loss and Resistivity for Transparent Flexible Electrodes.

    Science.gov (United States)

    Zhou, Hua; Xie, Jing; Mai, Manfang; Wang, Jing; Shen, Xiangqian; Wang, Shuying; Zhang, Lihua; Kisslinger, Kim; Wang, Hui-Qiong; Zhang, Jinxing; Li, Yu; Deng, Junhong; Ke, Shanming; Zeng, Xierong

    2018-05-09

    Transparent flexible electrodes are in ever-growing demand for modern stretchable optoelectronic devices, such as display technologies, solar cells, and smart windows. Such sandwich-film-electrodes deposited on polymer substrates are unattainable because of the low quality of the films, inducing a relatively large optical loss and resistivity as well as a difficulty in elucidating the interference behavior of light. In this article, we report a high-quality AZO/Au/AZO sandwich film with excellent optoelectronic performance, e.g., an average transmittance of about 81.7% (including the substrate contribution) over the visible range, a sheet resistance of 5 Ω/sq, and a figure-of-merit (FoM) factor of ∼55.1. These values are well ahead of those previously reported for sandwich-film-electrodes. Additionally, the interference behaviors of light modulated by the coat and metal layers have been explored with the employment of transmittance spectra and numerical simulations. In particular, a heater device based on an AZO/Au/AZO sandwich film exhibits high performance such as short response time (∼5 s) and uniform temperature field. This work provides a deep insight into the improvement of the film quality of the sandwich electrodes and the design of high-performance transparent flexible devices by the application of a flexible substrate with an atomically smooth surface.

  3. Enhancing the photovoltaic performance of bulk heterojunction polymer solar cells by adding Rhodamine B laser dye as co-sensitizer.

    Science.gov (United States)

    Kazemifard, Sholeh; Naji, Leila; Afshar Taromi, Faramarz

    2018-04-01

    Ternary blend (TB) strategy has been considered as an effective method to enhance the photovoltaic performance of bulk heterojunction (BHJ) polymer solar cells (PSCs). Here, we report on TB-based PSCs containing two donor materials; poly-3-hexylthiophene (P3HT) and Rhodamine B (RhB) laser organic dye, and [6,6]-phenyl C 61 butyric acid methyl ester (PC 61 BM) as an acceptor. The influence of RhB weight percentage and injection volume was extensively studied. To gain insight into the influences of RhB on the photovoltaic performance of PSCs, physicochemical and optical properties of TBs were compared with those of BHJ binary blend as a standard. RhB broadened the light absorption properties of the active layer and played a bridging role between P3HT and PC 61 BM. The PCE and short-circuit current density (Jsc) of the optimized TB-based PSCs comprising of 0.5 wt% RhB reached 5% and 12.12 mA/cm 2 , respectively. Compared to BHJ standard cell, the PCE and the generated current was improved by two orders of magnitude due to higher photon harvest of the active layer, cascade energy level structure of TB components and a considerable decrease in the charge carrier recombination. The results suggest that RhB can be considered as an effective material for application in PSCs to attain high photovoltaic performance. Copyright © 2018 Elsevier Inc. All rights reserved.

  4. Preparation and characterization of pyrromethene-567 dye-doped polymer samples using Gamma Irradiation Polymerization Method (GIPM)

    Energy Technology Data Exchange (ETDEWEB)

    Al-Ghamdi, Attieh A., E-mail: aaaalghamdi4@kau.edu.sa [Center of Nanotechnology, King Abdulaziz University, Jeddah (Saudi Arabia); Mahrous, Eiman M. [Taibah University, Department of Physics, Madinah (Saudi Arabia); Al-Enizi, Abdullah M. [King Saud University, Department of Chemistry, Riyadh (Saudi Arabia); Azam, Ameer [Center of Nanotechnology, King Abdulaziz University, Jeddah (Saudi Arabia)

    2015-01-15

    Dye-doped polymer gain media laser samples of pyrromethene-567 in a mixture with methyl methacrylate and 2-hydroxyethyl methacrylate copolymer have been prepared and synthesized by the Conventional Thermal Polymerization Method (CTPM) using an oven, and by the Gamma Irradiation Polymerization Method (GIPM) using Cobalt-60 ({sup 60}Co). Physical properties comprising absorption molar coefficients, absorption cross sections, fluorescence quantum yields, fluorescence life times, and emission cross sections were determined and calculated from the measured absorption and emission spectra. The efficiency and photo-stability of samples fabricated by both methods were measured and compared. The time required for synthesis was reduced by 90% using the GIPM. Complete polymerization of the GIPM sample was found to be at 7 kGy. Further, the GIPM produces high laser damage resistance material, which might be attributed to the highly dense polymeric network structure formed as a result of the effect of gamma radiation on MMA and HEMA monomers. - Highlights: • Samples of PM-567 in a mixture with MMA/HEMA were synthesized by the GIPM. • The time required for synthesis was reduced by 90% using the GIPM. • Complete polymerization of the GIPM sample was at 7 kGy. • The laser media produced is fast and free of contamination that gives high purity material. • The GIPM produced a high laser damage resistance material.

  5. Successful treatment of high azo dye concentration wastewater using combined anaerobic/aerobic granular activated carbon-sequencing batch biofilm reactor (GAC-SBBR): simultaneous adsorption and biodegradation processes.

    Science.gov (United States)

    Hosseini Koupaie, E; Alavi Moghaddam, M R; Hashemi, S H

    2013-01-01

    The application of a granular activated carbon-sequencing batch biofilm reactor (GAC-SBBR) for treatment of wastewater containing 1,000 mg/L Acid Red 18 (AR18) was investigated in this research. The treatment system consisted of a sequencing batch reactor equipped with moving GAC as biofilm support. Each treatment cycle consisted of two successive anaerobic (14 h) and aerobic (8 h) reaction phases. Removal of more than 91% chemical oxygen demand (COD) and 97% AR18 was achieved in this study. Investigation of dye decolorization kinetics showed that the dye removal was stimulated by the adsorption capacity of the GAC at the beginning of the anaerobic phase and then progressed following a first-order reaction. Based on COD analysis results, at least 77.8% of the dye total metabolites were mineralized during the applied treatment system. High-performance liquid chromatography analysis revealed that more than 97% of 1-naphthyalamine-4-sulfonate as one of the main sulfonated aromatic constituents of AR18 was removed during the aerobic reaction phase. According to the scanning electron microscopic analysis, the microbial biofilms grew in most cavities and pores of the GAC, but not on the external surfaces of the GAC.

  6. Mechanisms of reversible photodegradation in disperse orange 11 dye doped in PMMA polymer

    International Nuclear Information System (INIS)

    Embaye, Natnael B.; Ramini, Shiva K.; Kuzyk, Mark G.

    2008-01-01

    We use amplified spontaneous emission (ASE) and linear absorption spectroscopy to study the mechanisms of reversible photodegradation of 1-amino-2-methylanthraquinone (disperse orange 11-DO11) in solid poly(methyl methacrylate). Measurements as a function of intensity, concentration, and time suggest that ASE originates in a state (be it a tautomer or a vibronic level) that can form a dimer or some other aggregate upon relaxation, which through fluorescence quenching leads to degradation of the ASE signal. Whatever the degradation route, a high concentration of DO11 is required and the polymer plays a key role in the process of opening a new reversible degradation pathway that is not available at lower concentrations or in liquid solutions. We construct an energy level diagram that describes all measured quantities in the decay and recovery processes and propose a hypothesis of the nature of the associated states

  7. Optical gain at 650 nm from a polymer waveguide with dye-doped cladding

    Science.gov (United States)

    Reilly, M. A.; Coleman, B.; Pun, E. Y. B.; Penty, R. V.; White, I. H.; Ramon, M.; Xia, R.; Bradley, D. D. C.

    2005-12-01

    Signal amplification at the polymer optical fiber low-loss window of 650 nm is reported in an SU8 rib waveguide coated with Rhodamine-640 doped poly(methyl methacrylate). A signal beam is end-fired into the facet of a 7×100μm waveguide and amplified by top pumping of the 2-μm-thick cladding region with a pulsed pump source focused into a 9-mm-long stripe. A gain of 14dB and a minimum signal-to-noise ratio of around 2 dB are achieved in a 15-mm-long device with a low threshold pump intensity of 0.25μJ/mm2, which is an order of magnitude lower than previously reported.

  8. Comparative studies on dyeing rate migration and wash fastness ...

    African Journals Online (AJOL)

    Migration and diffusion properties of synthesized azo dyes from 2-aminothiazole derivatives applied on commercial grade undyed cellulose acetate (CA) and cellulose triacetate (CTA) were investigated using dyeing conditions of 2% on weight of fabric (owf), 50:1 liquor ratio and subjected to ISO3 and ISO4 standard wash ...

  9. The polymer gel electrolyte based on poly(methyl methacrylate) and its application in quasi-solid-state dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Yang Hongxun; Huang Miaoliang; Wu Jihuai; Lan Zhang; Hao Sancun; Lin Jianming

    2008-01-01

    Using poly(methyl methacrylate) as polymer host, ethylene carbonate, 1,2-propanediol carbonate and dimethyl carbonate as organic mixture solvents, sodium iodide and iodine as source of I - /I 3 - , a polymer gel electrolyte PMMA-EC/PC/DMC-NaI/I 2 with ionic conductivity of 6.89 mS cm -1 was prepared. Based on the polymer gel electrolyte, a quasi-solid-state dye-sensitized solar cell (DSSC) was fabricated. The quasi-solid-state DSSC possessed a good long-term stability and a light-to-electrical energy conversion efficiency of 4.78% under irradiation of 100 mW cm -2 simulated sunlight, which is almost equal to that of DSSC with a liquid electrolyte

  10. Experimental elaboration and analysis of dye-sensitized TiO2 solar cells (DSSC) dyed by natural dyes and conductive polymers

    Science.gov (United States)

    KałuŻyński, P.; Maciak, E.; Herzog, T.; Wójcik, M.

    2016-09-01

    In this paper we propose low cost and easy in development fully working dye-sensitized solar cell module made with use of a different sensitizing dyes (various anthocyanins and P3HT) for increasing the absorption spectrum, transparent conducting substrates (vaccum spattered chromium and gold), nanometer sized TiO2 film, iodide and methyl viologen dichloride based electrolyte, and a counter electrode (vaccum spattered platinum or carbon). Moreover, some of the different technologies and optimization manufacturing processes were elaborated for energy efficiency increase and were presented in this paper.

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

    Institute of Scientific and Technical Information of China (English)

    Yuanfang Wang; Baoyu Gao; Qinyan Yue; Yah Wang

    2011-01-01

    A coagulation/flocculation process using the composite floceulant 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 (η),basicity (B =[OH]/[Al]) and organic content (Wp) on the flocculation performance as well as the mechanism of PAC-EPI-DMA flocculant were investigated.The η was the key factor affecting the dye removal efficiency of PAC-EPI-DMA.PAC-EPI-DMA with an intermediate η (2400 mPa-sec) gave higher decolorization efficiency by adsorption bridging and charge neutralization due to the co-effect of PAC and EPI-DMA polymers.The Wp of the composite flocculant was a minor important factor for the flocculation.The adsorption bridging of PAC-EPI-DMA with η of 300 or 4300 mPa.sec played an important role with the increase of Wp,whereasthe charge neutralization of them was weaker with the increase of Wp.There was interaction between Wp 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.

  12. Decolorization of dyes by recombinase CotA from Escherichia coli ...

    African Journals Online (AJOL)

    The CotA laccase could efficiently decolorize anthraquinone and azo dyes in 24 h. The decolourization capacity of this recombinant laccase suggested that it could be a useful biocatalyst for the treatment of dye-containing effluents. Key words: Recombinant CotA laccase, Escherichia coli, purification, dye decolorization.

  13. Novel, one-step synthesis of zwitterionic polymer nanoparticles via distillation-precipitation polymerization and its application for dye removal membrane.

    Science.gov (United States)

    Ibrahim, G P Syed; Isloor, Arun M; Inamuddin; Asiri, Abdullah M; Ismail, Norafiqah; Ismail, Ahmed Fauzi; Ashraf, Ghulam Md

    2017-11-21

    In this work, poly(MBAAm-co-SBMA) zwitterionic polymer nanoparticles were synthesized in one-step via distillation-precipitation polymerization (DPP) and were characterized. [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (SBMA) as monomer and N, N'-methylene bis(acrylamide) (MBAAm) as cross-linker are used for the synthesis of nanoparticles. As  far as our knowledge, this is the first such report on the synthesis of poly(MBAAm-co-SBMA) nanoparticles via DPP. The newly synthesized nanoparticles were further employed for the surface modification of polysulfone (PSF) hollow fiber membranes for dye removal. The modified hollow fiber membrane exhibited the improved permeability (56 L/ m 2 h bar) and dye removal (>98% of Reactive Black 5 and >80.7% of Reactive orange 16) with the high permeation of salts. Therefore, the as-prepared membrane can have potential application in textile and industrial wastewater treatment.

  14. Influence of dehydrated nanotubed titanic acid on charge transport and luminescent properties of polymer light-emitting diodes with fluorescent dye

    Science.gov (United States)

    Qian, Lei; Bera, Debasis; Jin, Zhen-Sheng; Du, Zu-Liang; Xu, Zheng; Teng, Feng; Liu, Wei

    2007-09-01

    In this paper, we discuss the influence of dehydrated nanotubed titanic acid (DNTA) on charge transport and luminescent properties of polymer light-emitting diodes (PLEDs) doped with fluorescent dye. Photoluminescence results confirm the efficient energy transfer from PVK to 4-(dicyanom-ethylene)-2- t-butyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJTB) and tris-(8-hydroxtquinoline) aluminum (Alq 3) in a DNTA-doped device. The device showed lower turn-on voltages and higher charge current by doping with DNTA, which also caused a shift in the exciton's recombination region.

  15. Microbial fuel cell operation using monoazo and diazo dyes as terminal electron acceptor for simultaneous decolourisation and bioelectricity generation

    International Nuclear Information System (INIS)

    Oon, Yoong-Sin; Ong, Soon-An; Ho, Li-Ngee; Wong, Yee-Shian; Oon, Yoong-Ling; Lehl, Harvinder Kaur; Thung, Wei-Eng; Nordin, Noradiba

    2017-01-01

    Highlights: • Monoazo and diazo dyes were used as electron acceptor in the abiotic cathode of MFC. • Simultaneous decolourisation and bioelectricity generation were achieved. • Azo dye structures influenced the decolourisation performance. • Positive relation between decolourisation rate and power performance. - Abstract: Monoazo and diazo dyes [New coccine (NC), Acid orange 7 (AO7), Reactive red 120 (RR120) and Reactive green 19 (RG19)] were employed as electron acceptors in the abiotic cathode of microbial fuel cell. The electrons and protons generated from microbial organic oxidation at the anode which were utilized for electrochemical azo dye reduction at the cathodic chamber was successfully demonstrated. When NC was employed as the electron acceptor, the chemical oxygen demand (COD) removal and dye decolourisation efficiencies obtained at the anodic and cathodic chamber were 73 ± 3% and 95.1 ± 1.1%, respectively. This study demonstrated that the decolourisation rates of monoazo dyes were ∼50% higher than diazo dyes. The maximum power density in relation to NC decolourisation was 20.64 mW/m"2, corresponding to current density of 120.24 mA/m"2. The decolourisation rate and power output of different azo dyes were in the order of NC > AO7 > RR120 > RG19. The findings revealed that the structure of dye influenced the decolourisation and power performance of MFC. Azo dye with electron-withdrawing group at para substituent to azo bond would draw electrons from azo bond; hence the azo dye became more electrophilic and more favourable for dye reduction.

  16. Microbial fuel cell operation using monoazo and diazo dyes as terminal electron acceptor for simultaneous decolourisation and bioelectricity generation

    Energy Technology Data Exchange (ETDEWEB)

    Oon, Yoong-Sin [Water Research Group (WAREG), School of Environmental Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis (Malaysia); Ong, Soon-An, E-mail: ongsoonan@yahoo.com [Water Research Group (WAREG), School of Environmental Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis (Malaysia); Ho, Li-Ngee [School of Materials Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis (Malaysia); Wong, Yee-Shian; Oon, Yoong-Ling; Lehl, Harvinder Kaur; Thung, Wei-Eng [Water Research Group (WAREG), School of Environmental Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis (Malaysia); Nordin, Noradiba [School of Materials Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis (Malaysia)

    2017-03-05

    Highlights: • Monoazo and diazo dyes were used as electron acceptor in the abiotic cathode of MFC. • Simultaneous decolourisation and bioelectricity generation were achieved. • Azo dye structures influenced the decolourisation performance. • Positive relation between decolourisation rate and power performance. - Abstract: Monoazo and diazo dyes [New coccine (NC), Acid orange 7 (AO7), Reactive red 120 (RR120) and Reactive green 19 (RG19)] were employed as electron acceptors in the abiotic cathode of microbial fuel cell. The electrons and protons generated from microbial organic oxidation at the anode which were utilized for electrochemical azo dye reduction at the cathodic chamber was successfully demonstrated. When NC was employed as the electron acceptor, the chemical oxygen demand (COD) removal and dye decolourisation efficiencies obtained at the anodic and cathodic chamber were 73 ± 3% and 95.1 ± 1.1%, respectively. This study demonstrated that the decolourisation rates of monoazo dyes were ∼50% higher than diazo dyes. The maximum power density in relation to NC decolourisation was 20.64 mW/m{sup 2}, corresponding to current density of 120.24 mA/m{sup 2}. The decolourisation rate and power output of different azo dyes were in the order of NC > AO7 > RR120 > RG19. The findings revealed that the structure of dye influenced the decolourisation and power performance of MFC. Azo dye with electron-withdrawing group at para substituent to azo bond would draw electrons from azo bond; hence the azo dye became more electrophilic and more favourable for dye reduction.

  17. Optimal decolorization and kinetic modeling of synthetic dyes by Pseudomonas strains.

    Science.gov (United States)

    Yu, J; Wang, X; Yue, P L

    2001-10-01

    Pseudomonas spp were isolated from an anaerobic-aerobic dyeing house wastewater treatment facility as the most active azo-dye degraders. Decolorization of azo dyes and non-azo dyes including anthraquinone, metal complex and indigo was compared with individual strains and a bacterial consortium consisting of the individual strain and municipal sludge (50 50wt). The consortium showed a significant improvement on decolorization of two recalcitrant non-azo dyes, but little effect on the dyes that the individual strains could degrade to a great or moderate extent. Decolorization of Acid violet 7 (monoazo) by a Pseudomonas strain GM3 was studied in detail under various conditions. The optimum decolorization activity was observed in a narrow pH range (7-8), a narrow temperature range (35-40 degrees C), and at the presence of organic and ammonium nitrogen. Nitrate had a severe inhibitory effect on azo dye decolorization: 10 mg/L led to 50% drop in decolorization activity and 1000 mg/L to complete activity depression. A kinetic model is established giving the dependence of decolorization rate on cell mass concentration (first-order) and dye concentration (half order). The rate increased with temperature from 10 to 35 C, which can be predicted by Arrhenius equation with the activation energy of 16.87 kcal/mol and the frequency factor of 1.49 x 10(11) (mg L)1/2/g DCM min.

  18. Synthesis and characterization of 5-amino-2-((3-hydroxy-4-((3-hydroxyphenyl phenyl diazenyl phenol and its Cu(II complex – a strategy toward developing azo complexes for reduction of cytotoxicity

    Directory of Open Access Journals (Sweden)

    Durba Ganguly

    2014-12-01

    Full Text Available A major drawback of azo compounds is their associated toxicity, often carcinogenic, which is related to the reduction of the azo bond. This study intends to re-investigate this behavior by studying 5-amino-2-((3-hydroxy-4-((3-hydroxyphenyl phenyl diazenyl phenol (AHPD, a compound containing two azo bonds. Interaction of AHPD and its dimeric Cu(II complex with bacterial strains Escherichia coli and Staphylococcus aureus revealed the complex was less toxic. Reductive cleavage of the azo bond in AHPD and the complex followed using cytochrome c reductase (a model azo-reductase as well as azo-reductase enzymes obtained from bacterial cell extracts. Degradation of the azo bond was less in the complex allowing us to correlate the observed cytotoxicity. Cyclic voltammetry on AHPD and the complex support observations of enzyme assay experiments. These were particularly useful in realizing the formation of amines as an outcome of the reductive cleavage of azo bonds in AHPD that could not be identified through an enzyme assay. Results suggest that complex formation of azo compounds could be a means to control the formation of amines responsible for cytotoxicity. Studies carried out on bacterial cells for mere simplicity bear significance for multicellular organisms and could be important for human beings involved with the preparation and utilization of azo dyes.

  19. 40 CFR 721.2577 - Copper complex of (substituted sulfonaphthyl azo substituted phenyl) disulfonaphthyl azo, amine...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Copper complex of (substituted... Copper complex of (substituted sulfonaphthyl azo substituted phenyl) disulfonaphthyl azo, amine salt... substances identified generically as copper complex of (substituted sulfonaphthyl azo substituted phenyl...

  20. A Polymer Electrolyte for Dye-Sensitized Solar Cells Based on a Poly(Polyvinylidenefluoride-Co-Hexafluoropropylene)/Hydroxypropyl Methyl Cellulose Blend

    Science.gov (United States)

    Won, Lee Ji; Kim, Jae Hong; Thogiti, Suresh

    2018-03-01

    A novel polymer blend electrolyte for dye-sensitized solar cells (DSSCs) was synthesized by quasi-solidifying a liquid-based electrolyte containing an iodide/triiodide redox couple and supporting salts with a mixture of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and indigenous hydroxypropyl methyl cellulose (HPMC). A high ionic conductivity of 8.8 × 10-4 S cm-1 was achieved after introducing 5 wt% of HPMC with respect to the weight of PVDH-HFP. DSSCs were fabricated using gel polymer blend electrolytes, and the J-V characteristics of the fabricated devices were analyzed. Under optimal conditions, the photovoltaic conversion efficiency of cells with the novel HPMC-blended gel electrolyte (5.34%) was significantly greater than that of cells without HPMC (3.97%).

  1. The Effect of Lithium Iodide to the Properties of Carboxymethyl κ-Carrageenan/Carboxymethyl Cellulose Polymer Electrolyte and Dye-Sensitized Solar Cell Performance

    Directory of Open Access Journals (Sweden)

    Siti Rudhziah Che Balian

    2016-05-01

    Full Text Available This study was undertaken to investigate the solid biopolymer electrolytes based on a carboxymethyl κ-carrageenan/carboxymethyl cellulose blend complexed with lithium iodide of various weight ratios. The complexation of the doping salt with the polymer blend was confirmed by Fourier transform infrared spectroscopy. Ionic conductivity of the film was determined by impedance spectroscopy in the frequency range of 10 Hz to 4 MHz and in the temperature range of 303–338 K. The ionic conductivity increased with the increase in lithium iodide concentration as well as temperature. The membrane comprising 30 wt % of lithium iodide was found to give the highest conductivity of 3.89 × 10−3 S·cm−1 at room temperature. The increase in conductivity was associated with the increase in the number as well as the mobility of the charge carries. The conductivity increase with temperature followed the Vogel–Tamman–Fulcher model. The fabricated dye-sensitive solar cell, FTO/TiO2-dye/CMKC/CMCE-LiI (30 wt % +I2/Pt exhibited the highest conversion efficiency of 0.11% at a light intensity of 100 mW·cm−2. This indicated that the biopolymer blend electrolyte system has potential for use in dye-sensitized solar cells.

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

    Science.gov (United States)

    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

  3. Syntheses, structures and selective dye adsorption of five formic-based coordination polymers prepared by in-situ hydrolysis of N, N′-dimethylformamide

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Zheng; Meng, Xiang-min; Zhang, Dong-mei; Zhang, Xia; Wang, Mei [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, Shandong 266100 (China); Jin, Fan [Max Planck Institute for Terrestrial Microbiology & LOEWE Center for Synthetic Microbiology (SYNMIKRO), Marburg 35043 (Germany); Fan, Yu-hua [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, Shandong 266100 (China)

    2017-04-15

    Five functional coordination polymers (formic-based CPs) namely: ([Cu{sub 2}(CHOO){sub 3}(bibp){sub 2}]·CHOO){sub n} (1), ([Co{sub 2}(CHOO){sub 3}(bibp){sub 2}]·NO{sub 3}·H{sub 2}O)n (2), ([Ni{sub 2}(CHOO){sub 3}(bibp){sub 2}]·NO{sub 3}·H{sub 2}O){sub n} (3) [Co(CHOO){sub 2}(bbibp)]{sub n} (4) and [Zn(CHOO){sub 2}(bbibp)]{sub n} (5) (bibp=4,4′-bis(imidazolyl)biphenyl, bbibp=4,4′-bis(benzoimidazo-1-yl)biphenyl) have been successfully hydrothermally synthesized using the in-situ hydrolysis of N, N′-dimethylformamide (DMF) as the source of formate. All of these five polymers were characterized by single-crystal X-ray diffraction, elemental analysis, IR spectra, powder X-ray diffraction (PXRD), and thermogravimetric (TG) analysis. Complexes 1–3 have the similar three-dimensional 3D kag topological framework built from the bibp ligand as the support member between the neighboring formic planes. Both complexes 4 and 5 have the similar one-dimensional 1D linear chain which is further assembled into 3D supermolecular structure by C–H…O hydrogen bonds. The dyes adsorption experiments have also been investigated systematically. The results show that complexes 2 and 3 exhibit high selective adsorption ability towards anionic dyes in their aqueous solution. Moreover, complex 2 displays good reversibility in the process of the dyes adsorption-release. Meanwhile, the unusual blocking phenomenon was firstly observed when complex 2 was in MO/OIV aqueous solutions with different concentration.

  4. Microfluidic Dye Lasers

    DEFF Research Database (Denmark)

    Kristensen, Anders; Balslev, Søren; Gersborg-Hansen, Morten

    2006-01-01

    A technology for miniaturized, polymer based lasers, suitable for integration with planar waveguides and microfluidic networks is presented. The microfluidic dye laser device consists of a microfluidic channel with an embedded optical resonator. The devices are fabricated in a thin polymer film...

  5. Novel colorimetric sensors for cyanide based on azo-hydrazone tautomeric skeletons.

    Science.gov (United States)

    Adegoke, Olajire A; Adesuji, Temitope E; Thomas, Olusegun E

    2014-07-15

    The monoazo dyes, 4-carboxyl-2, 6-dinitrophenylazohydroxynaphthalenes dyes (AZ-01, AZ-03 and AZ-04), were evaluated as a highly selective colorimetric chemosensor for cyanide ion. The recognition of cyanide ion gave an obvious colour change from light yellow to brownish red and upon dilution with acetone produced a purple to lilac colour. Optimum conditions for the reaction between the azo dyes and cyanide ion were established at 30°C for 5 min, and different variables affecting the reaction were carefully studied and optimised. Under the optimum conditions, linear relationships between the CN(-) concentrations and light absorption were established. Using these azo-hydrazone molecular switch entities, excellent selectivity towards the detection of CN(-) in aqueous solution over miscellaneous competitive anions was observed. Such selectivity mainly results from the possibility of nucleophilic attack on the azo-hydrazone chemosensors by cyanide anions in aqueous system, which is not afforded by other competing anions. The cyanide chemosensor method described here should have potential application as a new family probes for detecting cyanide in aqueous solution. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Ultrasound assisted extraction of natural dye from jackfruit's wood (Artocarpus heterophyllus): The effect of ethanol concentration as a solvent

    Science.gov (United States)

    Febriana, Ike Dayi; Gala, Selfina; Mahfud, Mahfud

    2017-05-01

    Azo dye are synthetic organic dyes which has an azo group (- N = N -) as chromophore. Azo dye is resistand to decomposition process and harmfull for the environment and human being. Natural dye can be used as substitution of azo dye at textile industry. Natural dye are eco - friendly and can be applied for dyeing of fibrous material. Natural dye can be obtained from natural origin such as leaves, wood, or roots. The wood of jackfruit (Artocarpus heterophyllus) can used as natural source of natural dye. Ultrasound assisted extraction (UAE) is a new method that can be used to extract natural dye from jackfruit's wood. The aim of this research are to study about influence of ethanol concentration as solvent and extraction kinetic. Jackfruit's wood dust from sawmill used for the experimentation were sifted by sieve 35 mesh. Ethanol 96% used as solvent of this experiment and varied the concentration in volume to volume ratio (v/v). Experiment were carried out from 20 to 50 minutes. The result of this experiment shows that ethanol concentration influenced yield of extraction from jackfruit's wood. Concentration of ethanol will be affected polarity of solvent. The Peleg model was used to describe about kinetic model of natural dye extraction. Value of k1 and k2 constant are 0.003835 and 0.04186 respectively.

  7. pH triggered superior selective adsorption and separation of both cationic and anionic dyes and photocatalytic activity on a fully exfoliated titanate layer-natural polymer based nanocomposite.

    Science.gov (United States)

    Sarkar, Amit Kumar; Saha, Arka; Panda, Asit Baran; Pal, Sagar

    2015-11-18

    A fully exfoliated titanate layer-natural polymer amylopectin based nanocomposite, with pH responsive superior selective adsorption, separation of both cationic (MB: 599 mg g(-1) at pH 9) and anionic (MO: 558 mg g(-1) at pH 3) dyes and photodegradation properties, has been realized through simultaneous in situ layered titanate formation, exfoliation and polymerization.

  8. Study of Modern Nano Enhanced Techniques for Removal of Dyes and Metals

    Directory of Open Access Journals (Sweden)

    Samavia Batool

    2014-01-01

    Full Text Available Industrial effluent often contains the significant amount of hexavalent chromium and synthetic dyes. The discharge of wastewater without proper treatment into water streams consequently enters the soil and disturbs the aquatic and terrestrial life. A range of wastewater treatment technologies have been proposed which can efficiently reduce both Cr(VI and azo dyes simultaneously to less toxic form such as biodegradation, biosorption, adsorption, bioaccumulation, and nanotechnology. Rate of simultaneous reduction of Cr(VI and azo dyes can be enhanced by combining different treatment techniques. Utilization of synergistic treatment is receiving much attention due to its enhanced efficiency to remove Cr(VI and azo dye simultaneously. This review evaluates the removal methods for simultaneous removal of Cr(VI and azo dyes by nanomicrobiology, surface engineered nanoparticles, and nanophotocatalyst. Sorption mechanism of biochar for heavy metals and organic contaminants is also discussed. Potential microbial strains capable of simultaneous removal of Cr(VI and azo dyes have been summarized in some details as well.

  9. Competitive effects of humic acid and wastewater on adsorption of Methylene Blue dye by activated carbon and non-imprinted polymers.

    Science.gov (United States)

    Murray, Audrey; Örmeci, Banu

    2018-04-01

    Natural organic matter (NOM), present in natural waters and wastewater, decreases adsorption of micropollutants, increasing treatment costs. This research investigated mechanisms of competition for non-imprinted polymers (NIPs) and activated carbon with humic acid and wastewater. Three different types of activated carbons (Norit PAC 200, Darco KB-M, and Darco S-51) were used for comparison with the NIP. The lower surface area and micropore to mesopore ratio of the NIP led to decreased adsorption capacity in comparison to the activated carbons. In addition, experiments were conducted for single-solute adsorption of Methylene Blue (MB) dye, simultaneous adsorption with humic acid and wastewater, and pre-loading with humic acid and wastewater followed by adsorption of MB dye using NIP and Norit PAC 200. Both the NIP and PAC 200 showed significant decreases of 27% for NIP (p=0.087) and 29% for PAC 200 (p=0.096) during simultaneous exposure to humic acid and MB dye. There was no corresponding decrease for NIP or PAC 200 pre-loaded with humic acid and then exposed to MB. In fact, for PAC 200, the adsorption capacity of the activated carbon increased when it was pre-loaded with humic acid by 39% (p=0.0005). For wastewater, the NIP showed no significant increase or decrease in adsorption capacity during either simultaneous exposure or pre-loading. The adsorption capacity of PAC 200 increased by 40% (p=0.001) for simultaneous exposure to wastewater and MB. Pre-loading with wastewater had no effect on MB adsorption by PAC 200. Copyright © 2017. Published by Elsevier B.V.

  10. AZO-Ag-AZO transparent electrode for amorphous silicon solar cells

    International Nuclear Information System (INIS)

    Theuring, Martin; Vehse, Martin; Maydell, Karsten von; Agert, Carsten

    2014-01-01

    Metal-based transparent electrodes can be fabricated at low temperatures, which is crucial for various substrate materials and solar cells. In this work, an oxide-metal-oxide (OMO) transparent electrode based on aluminum zinc oxide (AZO) and silver is compared to AZO layers, fabricated at different temperatures and indium tin oxides. With the OMO structure, a sheet resistance of 7.1/square and a transparency above 80% for almost the entire visible spectrum were achieved. The possible application of such electrodes on a textured solar cell was demonstrated on the example of a rough ZnO substrate. An OMO structure is benchmarked in a n-i-p amorphous silicon solar cell against an AZO front contact fabricated at 200 °C. In the experiment, the OMO electrode shows a superior performance with an efficiency gain of 30%. - Highlights: • Multilayer transparent electrode based on aluminum zinc oxide (AZO) and Ag • Comparison of AZO-Ag-AZO transparent electrode to AZO and indium tin oxide • Performance of AZO-Ag-AZO transparent electrodes on textured surfaces • Comparison of amorphous silicon solar cells with different transparent electrodes

  11. Novel salicylazo polymers for colon drug delivery: dissolving polymers by means of bacterial degradation.

    Science.gov (United States)

    Saphier, Sigal; Karton, Yishai

    2010-02-01

    Novel azo polymers were prepared for colonic drug delivery with a release mechanism based on structural features of azo derivatives designed for rapid bacterial degradation leading to soluble polymers. Two Salicylazo derivatives were prepared and conjugated as side chains at different ratios to methacrylic acid-methyl methacrylate copolymers (Eudragits). The azo compounds were designed to have a hydrophilic and a hydrophobic part on opposite sides of the azo bond. Upon reduction of the azo bonds, the hydrophobic part is released, resulting in a more water soluble polymer. The solubility of the polymeric films was studied relative to Eudragit S known to dissolve toward the end of the small intestine. One of the two azo derivatives prepared gave rise to polymers, which showed reduced solubility relative to Eudragit S. These polymers were subjected to reduction tests in anaerobic rat cecal suspensions by following the release of the hydrophobic product. Reduction rate was found to be rapid, comparable to that of Sulfasalazine. Studies on the azopolymeric films in anaerobic rat cecal suspensions, showed that these polymers dissolve faster than in sterilized suspensions. Solid dosage forms may be coated with these polymers to provide an efficient delivery system to the colon with a rapid release mechanism. (c) 2009 Wiley-Liss, Inc. and the American Pharmacists Association.

  12. Methacrylic azopolymers for holographic storage: A comparison among different polymer types

    DEFF Research Database (Denmark)

    Forcen, P.; Oriol, L.; Sanchez, C.

    2007-01-01

    The photoinduced anisotropy and volume holographic storage in a series of polymers with different architectures and azo contents of 7% and 20% in weight have been investigated. Measurements of the birefringence (An) induced with nearly polarised 488 nm light show that for polymers with an azo con...

  13. Methacryluic Azopolymers for Holographic Storage: A Comparison among Different Polymer Types

    DEFF Research Database (Denmark)

    Forcén, Patricia; Oriol, Luis; Sánchez, Carlos

    2007-01-01

    The photoinduced anisotropy and volume holographic storage in a series of polymers with different architectures and azo contents of 7% and 20% in weight have been investigated. Measurements of the birefringence (An) induced with im- early polarised 488 nm light show that for polymers with an azo ...

  14. Nanostructured TiO2 microspheres for dye-sensitized solar cells employing a solid state polymer electrolyte

    International Nuclear Information System (INIS)

    Jung, Hun-Gi; Nagarajan, Srinivasan; Kang, Yong Soo; Sun, Yang-Kook

    2013-01-01

    Bimodal mesoporous, anatase TiO 2 microspheres with particle sizes ranging from 0.3 to 2 μm were synthesized using a facile solvothermal method. The photovoltaic performance of TiO 2 microspheres in dye-sensitized solar cells (DSSCs) using a solid state electrolyte was investigated. The solid state electrolyte DSSC device based on the TiO 2 microspheres exhibits an energy conversion efficiency of 4.2%, which is greater than that of commercial P25 TiO 2 (3.6%). The higher photocurrent density was primarily achieved as a result of the greater specific surface area and pore size, which resulted in an increase in the dye uptake of the TiO 2 microspheres and easy transport of solid electrolyte through mesopores. In addition, the greater electron lifetime and superior light scattering ability also enhanced the photovoltaic performance of the TiO 2 microsphere-based, solid state DSSCs

  15. A Novel Polymer Electrolyte Using In-situ Quanternization for All Solid-state Dye-sensitized Solar Cell

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    1 Introduction Dye-sensitized solar cells (DSSCs) with a mesoporous network of interconnected TiO2 nanocrystals have attracted wide-spread scientific and technological interest over the past decades due to its low cost and high energy conversion efficiency. Meantime, it also has been considered as potential alternative to conventional photovoltaic devices. In 2001, Gratzel group constructed such kind of DSSC with the conversion efficiency of more than 11%[1]. But this system uses liquid electrolyte with...

  16. Surface relief gratings: experiments, physical scenarios, and photoinduced (anomalous) dynamics of functionalized polymer chains

    Science.gov (United States)

    Mitus, A. C.; Radosz, W.; Wysoczanski, T.; Pawlik, G.

    2017-10-01

    Surface Relief Gratings (SRG) were demonstrated experimentally more than 20 years ago. Despite many years of research efforts the underlying physical mechanisms remain unclear. In this paper we present a short overview of the main concepts related to SRG - photofluidization and its counterpart, the orientational approach - based on a seminal paper by Saphiannikova et al. Next, we summarize the derivation of the cos2 θ potential, following the lines of recent paper of this group. Those results validate the generic Monte Carlo model for the photoinduced build-up of the density and SRG gratings in a model polymer matrix functionalized with azo-dyes, presented in another part of the paper. The characterization of the photoinduced motion of polymer chains, based on our recent paper, is briefly discussed in the last part of the paper. This discussion offers a sound insight into the mechanisms responsible for inscription of SRG as well as for single functionalized nanoparticle studies.

  17. A hydrazone covalent organic polymer based micro-solid phase extraction for online analysis of trace Sudan dyes in food samples.

    Science.gov (United States)

    Zhang, Chengjiang; Li, Gongke; Zhang, Zhuomin

    2015-11-06

    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

  18. Treatment of a Textile Effluent from Dyeing with Cochineal Extracts Using Trametes versicolor Fungus

    Directory of Open Access Journals (Sweden)

    Gabriela Arroyo-Figueroa

    2011-01-01

    Full Text Available 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.

  19. Treatment of a textile effluent from dyeing with cochineal extracts using Trametes versicolor fungus.

    Science.gov (United States)

    Arroyo-Figueroa, Gabriela; Ruiz-Aguilar, Graciela M L; López-Martínez, Leticia; González-Sánchez, Guillermo; Cuevas-Rodríguez, Germán; Rodríguez-Vázquez, Refugio

    2011-05-05

    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.

  20. Kinetic of Azo Dyes Decolourization by Enterobacteriaceae Species ...

    African Journals Online (AJOL)

    It was observed that the riboflavin addition at 19.95 n moles ml-1 in the reaction mixture, rate of decolourization was suddenly change from 0.019 ÄA/minutes to 0.20 ÄA/minutes, which is extremely high by 10 fold fast and subsequently remains faster i.e 0.2 ÄA/minutes without further additional RF in the same assay mixture.

  1. Decolorization of the azo dye reactive black 5 using laccase ...

    African Journals Online (AJOL)

    The PDF file you selected should load here if your Web browser has a PDF reader plug-in installed (for example, a recent version of Adobe Acrobat Reader). If you would like more information about how to print, save, and work with PDFs, Highwire Press provides a helpful Frequently Asked Questions about PDFs.

  2. Metal-free polymer/MWCNT composite fiber as an efficient counter electrode in fiber shape dye-sensitized solar cells

    Science.gov (United States)

    Ali, Abid; Mujtaba Shah, Syed; Bozar, Sinem; Kazici, Mehmet; Keskin, Bahadır; Kaleli, Murat; Akyürekli, Salih; Günes, Serap

    2016-09-01

    Highly aligned multiwall carbon nanotubes (MWCNT) as fiber were modified with a conducting polymer via a simple dip coating method. Modified MWCNT exhibited admirable improvement in electrocatalytic activity for the reduction of tri-iodide in dye sensitized solar cells. Scanning electron microscopy images confirm the successful deposition of polymer on MWCNT. Cyclic voltammetry, square wave voltammetry and electrochemical impedance spectroscopy studies were carried out to investigate the inner mechanism for the charge transfer behaviour. Results from bare and modified electrodes revealed that the MWCNT/(poly (3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) composite electrode is much better at catalysing the {{{{I}}}3}-/{{{I}}}- redox couple compared to the pristine fiber electrode. The photoelectric conversion efficiency of 5.03% for the modified MWCNT electrodes was comparable with that of the conventional Pt-based electrode. The scientific results of this study reveal that MWCNT/PEDOT:PSS may be a better choice for the replacement of cost intensive electrode materials such as platinum. Good performance even after bending up to 90° and in-series connection to enhance the output voltage were also successfully achieved, highlighting the practical application of this novel device.

  3. Bioremediation of acid fast red dye by Streptomyces globosus under ...

    African Journals Online (AJOL)

    Two different azo dyes known as acid fast red (AFR) and Congo red (CR) were examined for their decolorization by five strains of actinomycetes (Streptomyces globosus, Streptomyces alanosinicus, Streptomyces ruber, Streptomyces gancidicus, and Nocardiopsis aegyptia) under shake and static conditions. Streptomyces ...

  4. Bioremediation of acid fast red dye by Streptomyces globosus under ...

    African Journals Online (AJOL)

    Administrator

    2011-04-25

    Apr 25, 2011 ... Azo dyes are widely used in industries, such as textiles, paper, plastics ... processes have received increasing interest owing to their cost effectiveness and environmental friendliness. (Mabrouk and ... hydrolytic enzymes . In addition it .... A trial for using potato peels for more economic biomass production.

  5. FIA-Spectrophotometric Method for Determination of Nitrite in Meat Products: An Experiment Exploring Color Reduction of an Azo-Compound

    Science.gov (United States)

    Penteado, Jose C.; Angnes, Lucio; Masini, Jorge C.; Oliveira, Paulo C. C.

    2005-01-01

    This article describes the reaction between nitrite and safranine O. This sensitive reaction is based on the disappearance of color of the reddish-orange azo dye, allowing the determination of nitrite at the mg mL-1 level. A factorial optimization of parameters was carried out and the method was applied for the quantification of nitrite in…

  6. Platinum/titanium bilayer deposited on polymer film as efficient counter electrodes for plastic dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Ikegami, M.; Miyoshi, K.; Miyasaka, T.; Teshima, K.; Wei, T. C.; Wan, C. C.; Wang, Y. Y.

    2007-01-01

    A surface-rich platinum/titanium bilayer was deposited on poly(ethylene naphthalate) film by vacuum sputtering as counterelectrode for plastic dye-sensitized solar cells (DSSCs). Compared to the electrodes made of pure Pt layer, this electrode maintained similar electrochemical catalytic effect at relative low Pt usage. Current-voltage characteristics of the plastic DSSC at this stage stand at 0.69 V on V OC , 9.97 mA/cm 2 on I SC , 0.69 on fill factor, and 4.31% cell efficiency under AM1.5, 100 mW/cm 2 illumination

  7. Molecular and excited state properties of isomeric scarlet disperse dyes

    Science.gov (United States)

    Lim, Jihye; Szymczyk, Malgorzata; Mehraban, Nahid; Ding, Yi; Parrillo-Chapman, Lisa; El-Shafei, Ahmed; Freeman, Harold S.

    2018-06-01

    This work was part of an investigation aimed at characterizing the molecular and excited state properties of currently available disperse dyes developed to provide stability to extensive sunlight exposures when adsorbed on poly(ethylene terephthalate) (PET) fibers. Having completed the characterization of yellow, magenta, and cyan disperse dyes for PET-based fabrics used outdoors, our attention turned to the colors designed to enhance the color gamut of a standard 4-member (cyan/yellow/magenta/black) color set. The present study pertained specifically to the characterization of commercially available scarlet dyes. In this regard, HPLC analysis showed that a scarlet product used for PET coloration was mainly a 70/30 mixture of dyes, and the use of HRMS and single crystal X-ray diffraction analyses indicated that these two dyes were azo compounds derived from isomeric pyridine-based couplers which differed in the location of the primary amino (sbnd NH2) and anilino (sbnd NHPh) groups attached to the pyridine ring. One dye structure has the sbnd NHPh group para to the azo group (Sc2), while the other has that group in the ortho position (Sc3). The presence of either ortho substituent provides photostabilization through intramolecular H-bonding with the azo moiety. Further, results from molecular modeling studies showed that the lower excited state oxidation potential of Sc3 relative to that of Sc2 allows Sc3 to function as an energy quencher for the excited state of Sc2 - through thermodynamically favorable electron transfer.

  8. Thermal stability and degradation behavior of novel wholly aromatic azo polyamide-hydrazides

    International Nuclear Information System (INIS)

    Al-Ghamdia, R.F.; Fahmib, M.M.; Mohamed, N.A.

    2005-01-01

    Thermal stability and degradation behavior of a series of novel wholly aromatic azo polyamide-hydrazides have been investigated in nitrogen and in air atmospheres using differential scanning ealorimetry, thermogravimetry, infrared spectroscopy and elemental analysis. The influences of controlled structural variations and molecular weight on the thermal stability and degradation behavior of this series of polymers have also been studied. The structural differences were achieved by varying the content of para- and meta substituted phenylene rings incorporated within this series. The polymers were prepared by a low temperature solution polycondensation reaction of p aminosalicylic acid hydrazide and an equimolar amount of 4,4-azo dibenzoyl chloride [4,4 ADBC] or 3,3-azo dibenzoyl chloride [3,3ADBC] or mixtures of various molar ratios of 4,4ADBC and 3,3ADBC in anhydrous N,N- dimethyl acetamide [DMAc] containing lithium chloride as a solvent at -10 degree C. The results clearly reveal that these polymers are characterized by high thermal stability. Their weight loss occurred in three distinctive steps. The first was small and assigned to the evaporation of absorbed moisture. The second was appreciable and was attributed to the cyclo dehydration reaction of the hydrazide groups into 1,3,4-oxadiazole rings by losing water, combined with elimination of azo groups by losing molecular nitrogen. This is not a true degradation but rather a thermo-chemical transformation reaction of the azo polyamide-hydrasdes into the corresponding polyamide-l,3,4-oxadiazoles. The third was relatively severe and sharp, particularly in air, and corresponded to the decomposition of the resulting polyamide-l, 3,4-oxadiazoles. In both degradation atmospheres, the improved resistance to high temperatures was always associated with increased content of para- phenylene moieties of the investigated polymer. Further, with exception of 160-200 degree C temperature range, where the lower molecular weight

  9. A kinetic study of textile dyeing wastewater degradation by Penicillium chrysogenum.

    Science.gov (United States)

    Durruty, Ignacio; Fasce, Diana; González, Jorge Froilán; Wolski, Erika Alejandra

    2015-06-01

    The potential of Penicillium chrysogenum to decolorize azo dyes and a real industrial textile wastewater was studied. P. chrysogenum was able to decolorize and degrade three azo dyes (200 mg L(-1)), either independently or in a mixture of them, using glucose as a carbon source. A kinetic model for degradation was developed and it allowed predicting the degradation kinetics of the mixture of the three azo dyes. In addition, P. chrysogenum was able to decolorize real industrial wastewater. The kinetic model proposed was also able to predict the decolorization of the real wastewater. The calibration of the proposed model makes it a useful tool for future wastewater facilities' design and for practical applications.

  10. Structural evolution, electrical and optical properties of AZO films ...

    Indian Academy of Sciences (India)

    Administrator

    Aluminum-doped zinc oxide (AZO) target was fabricated using AZO ... All AZO films show c-axis preferred orientation and hexagonal structure. With increasing film thick- ness from 153 to 1404 nm, the crystallinity was improved and the angle of (002) peak was close to ... For observing grain boundary and size, the target was.

  11. Fabrication of Cost-Effective Dye-Sensitized Solar Cells Using Sheet-Like CoS2 Films and Phthaloylchitosan-Based Gel-Polymer Electrolyte

    Directory of Open Access Journals (Sweden)

    Saradh Prasad

    2018-01-01

    Full Text Available Platinum-free counter electrodes (CE were developed for use in efficient and cost-effective energy conversion devices, such as dye-sensitized solar cells (DSSCs. Electrochemical deposition of CoS2 on fluorine-doped tin oxide (FTO formed a hierarchical sheet-like structured CoS2 thin film. This film was engaged as a cost-effective platinum-free and high-efficiency CE for DSSCs. High stability was achieved using a phthaloychitosan-based gel-polymer electrolyte as the redox electrolyte. The electrocatalytic performance of the sheet-like CoS2 film was analyzed by electrochemical impedance spectroscopy and cyclic voltammetry. The film displayed improved electrocatalytic behavior that can be credited to a low charge-transfer resistance at the CE/electrolyte boundary and improved exchange between triiodide and iodide ions. The fabricated DSSCs with a phthaloychitosan-based gel-polymer electrolyte and sheet-like CoS2 CE had a power conversion efficiency (PCE, η of 7.29% with a fill factor (FF of 0.64, Jsc of 17.51 mA/cm2, and a Voc of 0.65 V, which was analogous to that of Pt CE (η = 7.82%. The high PCE of the sheet-like CoS2 CE arises from the enhanced FF and Jsc, which can be attributed to the abundant active electrocatalytic sites and enhanced interfacial charge-transfer by the well-organized surface structure.

  12. Azoreductase and dye detoxification activities of Bacillus velezensis strain AB.

    Science.gov (United States)

    Bafana, Amit; Chakrabarti, Tapan; Devi, Sivanesan Saravana

    2008-01-01

    Azo dyes are known to be a very important and widely used class of toxic and carcinogenic compounds. Although lot of research has been carried out for their removal from industrial effluents, very little attention is given to changes in their toxicity and mutagenicity during the treatment processes. Present investigation describes isolation of a Bacillus velezensis culture capable of degrading azo dye Direct Red 28 (DR28). Azoreductase enzyme was isolated from it, and its molecular weight was found to be 60 kDa. The enzyme required NADH as cofactor and was oxygen-insensitive. Toxicity and mutagenicity of the dye during biodegradation was monitored by using a battery of carefully selected in vitro tests. The culture was found to degrade DR28 to benzidine and 4-aminobiphenyl, both of which are potent mutagens. However, on longer incubation, both the compounds were degraded further, resulting in reduction in toxicity and mutagenicity of the dye. Thus, the culture seems to be a suitable candidate for further study for both decolourization and detoxification of azo dyes, resulting in their safe disposal.

  13. Irradiation treatment of textile dyes: Apollofix-red

    International Nuclear Information System (INIS)

    Wojnarovits, L.; Palfi, T.; Takacs, E.

    2004-01-01

    The UV-VIS absorption spectra of azo dyes in aqueous solutions strongly overlap with the spectra of intermediates produced in reaction with the intermediates of water radiolysis. This overlap complicates the investigation of reaction mechanisms. The paper describes a method for the separation of the two spectra on the example of Apollofix-Red, a triazine and H-acid containing dye. The reactivity of water radiolysis intermediates (e aq - , OH, H, O 2 /HO 2 ) with the dye is also discussed. The most intensive decolouration was found in the reaction of e aq - and H which is due to the fast reaction of these intermediates with the -N=N-azo group of the unreacted molecule and their slow reaction with the transformed molecules. (author)

  14. Electrical circuit model of ITO/AZO/Ge photodetector.

    Science.gov (United States)

    Patel, Malkeshkumar; Kim, Joondong

    2017-10-01

    In this data article, ITO/AZO/Ge photodetector was investigated for electrical circuit model. Due to the double (ITO and AZO) transparent metal-oxide films (DOI:10.1016/j.mssp.2016.03.007) (Yun et al., 2016) [1], the Ge heterojunction device has a better interface quality due to the AZO layer with a low electrical resistance due to the ITO layer (Yun et al., 2015) [2]. The electrical and interfacial benefitted ITO/AZO/Ge heterojunction shows the quality Schottky junction. In order to investigate the device, the ITO/AZO/Ge heterojunction was analyzed by R-C circuit model using the impedance spectroscopy.

  15. Construction of an integrated enzyme system consisting azoreductase and glucose 1-dehydrogenase for dye removal.

    Science.gov (United States)

    Yang, Yuyi; Wei, Buqing; Zhao, Yuhua; Wang, Jun

    2013-02-01

    Azo dyes are toxic and carcinogenic and are often present in industrial effluents. In this research, azoreductase and glucose 1-dehydrogenase were coupled for both continuous generation of the cofactor NADH and azo dye removal. The results show that 85% maximum relative activity of azoreductase in an integrated enzyme system was obtained at the conditions: 1U azoreductase:10U glucose 1-dehydrogenase, 250mM glucose, 1.0mM NAD(+) and 150μM methyl red. Sensitivity analysis of the factors in the enzyme system affecting dye removal examined by an artificial neural network model shows that the relative importance of enzyme ratio between azoreductase and glucose 1-dehydrogenase was 22%, followed by dye concentration (27%), NAD(+) concentration (23%) and glucose concentration (22%), indicating none of the variables could be ignored in the enzyme system. Batch results show that the enzyme system has application potential for dye removal. Copyright © 2012 Elsevier Ltd. All rights reserved.

  16. Modification of fluorescence and optical properties of Rhodamine B dye doped PVA/Chitosan polymer blend films

    Science.gov (United States)

    Padmakumari, R.; Ravindrachary, V.; Mahantesha, B. K.; Sagar, Rohan N.; Sahanakumari, R.; Bhajantri, R. F.

    2018-05-01

    Pure and Rhodamine B doped Poly (vinyl alcohol)/Chitosan composite films are prepared using solution casting method. Fourier transforms infrared spectra (FTIR), Ultraviolet-Visible (UV-Vis), fluorescence studies were used to characterize the prepared polymer films. The FT-IR results show that the appearance of new peaks along with shift in peak positions indicates the interaction of Rhodamine B with PVA-CS blend. Optical absorption edge, band gap and activation energy were determined from UV-Visible studies. The optical absorption edge increases, band gap decreases and activation energy increases with dopant concentration respectively. The corresponding emission spectra were studied using fluorescence spectroscopy. From the fluorescence study the quenching phenomena are observed in emission wavelength range of 607nm-613nm upon excitation with absorption maxima 443nm.

  17. Eco-friendly synthesis of 4-4-diaminodiphenylurea, a dye intermediate and direct dyes derived from it

    International Nuclear Information System (INIS)

    Amjad, R.; Khan, S.R.; Naeem, M.; Sohaib, M.; Munawar, M.A.

    2011-01-01

    A rapid, environmental friendly and highly efficient method for the synthesis of 4-4/sup '/-diaminodiphenyl- urea and direct dyes derived form it has been reported. The reported method is environmentally friendly, as it doesn't involve the usage of environmentally hazardous material like phosgene and tri phosgene. Novel azo dyes have been prepared by the coupling of 4-4/sup '/-Diamino diphenylurea with various couplers. Structure elucidation of the synthesized dyes was carried out by IR, NMR, Elemental analysis, and confirmation was made by Mass Spectrometry. The dyeing performance of these dyes was assessed on cotton fabric. The dye bath exhaustion, sublimation and fastness properties were also determined. The dyed fabric showed moderate to good light fastness and very good to excellent fastness properties for washing, rubbing, perspiration, and sublimation. (author)

  18. Degradation of a monoazo dye Alizarin Yellow GG in aqueous solutions by gamma irradiation: Decolorization and biodegradability enhancement

    International Nuclear Information System (INIS)

    Sun, Weihua; Chen, Lujun; Tian, Jinping; Wang, Jianlong; He, Shijun

    2013-01-01

    The irradiation-induced degradation of an azo dye, Alizarin Yellow GG (AY-GG), was investigated in aqueous solution under gamma irradiation using a 60 Cobalt source at a dose rate of 113 Gy/min. The decolorization percentage of AY-GG reached 65% when its initial concentration was 100 mg/l and the absorbed dose was 9 kGy. The decolorization process could be described by first-order kinetic equation. In addition, specific oxygen uptake rate (SOUR, mg O 2 (g MLVSS) −1 h −1 ) of activated sludge using the irradiated azo dye solutions was 8.1 mg O 2 (g MLVSS) −1 h −1 after 9 kGy irradiation, indicating that the biodegradability of AY-GG could be enhanced by 30%. However, toxic intermediates including heterocyclic aromatic amines and cyanides were detected during the irradiation process, which inhibited the complete biological degradation of azo dye. Fortunately, the inhibition could be eliminated by further irradiation. The azo dye solution became amenable to biodegradation and can be further treated by biological treatment process. - Highlights: ► Decolorization process by radiation conformed to first-order kinetics. ► Biodegradability of AY-GG could be enhanced 30% after 9 kGy radiation. ► Radiation can be used as a pretreatment technology for azo dye-containing wastewater. ► Combining radiation with aerobic biological treatment is a feasible strategy.

  19. Novel Tunable Dye Laser for Lidar Detection, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — A tunable dye laser for Lidar detection will be fabricated based on the innovative dye-doped Holographic Polymer Dispersed Liquid Crystals (HPDLC) technology. The...

  20. Homogenous and heterogenous advanced oxidation of two commercial reactive dyes.

    Science.gov (United States)

    Balcioglu, I A; Arslan, I; Sacan, M T

    2001-07-01

    Two commercial reactive dyes, the azo dye Reactive Black 5 and the copper phythalocyanine dye Reactive Blue 21, have been treated at a concentration of 75 mg l(-1) by titanium dioxide mediated photocatalytic (TiO2/UV), dark and UV-light assisted Fenton (Fe2+/H2O2) and Fenton-like (Fe3+/H2O2) processes in acidic medium. For the treatment of Reactive Black 5, all investigated advanced oxidation processes were quite effective in terms of colour, COD as well as TOC removal. Moreover, the relative growth inhibition of the azo dye towards the marine algae Dunaliella tertiolecta that was initially 70%, did not exhibit an increase during the studied advanced oxidation reactions and complete detoxification at the end of the treatment period could be achieved for all investigated treatment processes. However, for Reactive Blue 21, abatement in COD and UV-VIS absorbance values was mainly due to the adsorption of the dye on the photocatalyst surface and/or the coagulative effect of Fe3+/Fe2+ ions. Although only a limited fraction of the copper phythalocyanine dye underwent oxidative degradation, 47% of the total copper in the dye was already released after 1 h photocatalytic treatment.

  1. Studies on Synthesis and Dyeing Preformance of Acid Dyes Based on 4,7-Dihydroxy-1,10-Phenanthroline-2,9-Dione

    Directory of Open Access Journals (Sweden)

    B. V. Patel

    2008-01-01

    Full Text Available Some new azo acid dyes were prepared by coupling various diazotized acid components such as anthranilic acid, sulphanilic acid, laurent acid, peri acid, tobias acid, H-acid, J-acid, gamma acid, sulphotobias acid, 4-aminotoluiene-3-sulphonic acid, 5-sulpho- anthranilic acid, 2-naphthylamine-3,6,8-trisulphonic acid, bronner acid, metanilic acid and cleve acid with 4,7-dihydroxy-1,10-phenanthroline-2,9-dione. The dyes were characterized by elemental, IR and TLC analyses. Their dyeing performance as acid dyes has been assessed on viscose rayon, wool and cotton fibres.

  2. ADSORPSI-DESORPSI ZAT WARNA AZO JENIS REMAZOL BLACK B MENGGUNAKAN MEMBRAN POLIELEKTROLIT (PEC KITOSAN-PEKTIN

    Directory of Open Access Journals (Sweden)

    Ni Putu Sri Ayuni

    2016-08-01

    Full Text Available Abstrak Sekitar 2-50% dari zat warna azo yang digunakan selama proses pencelupan ini tidak mengikat serat dan langsung dilepaskan ke lingkungan melalui instalasi pengolahan limbah. Hal ini perlu dilakukan pengolahan limbah cair yang mengandung zat warna azo jenis Remazol Black B sebelum dibuang ke lingkungan. Penelitian ini bertujuan untuk mengetahui kondisi optimum membran PEC kitosan-pektin yang dapat digunakan untuk mengadsorpsi zat warna azo jenis Remazol Black B .Untuk memperoleh kondisi optimum akan dilakukan adsorpsi zat warna azo jenis Remazol Black B dengan variasi waktu kontak (5-150 menit, pH (5-9 dan konsentrasi larutan zat warna azo jenis Remazol Black B (5, 10, 15, 20, dan 25 mg/L. Untuk mengetahui karakteristik zat warna jenis Remazol Black B oleh membran PEC kitosan-pektin di analisis dengan persamaan isoterm adsorpsi Langmuir dan isoterm adsorpsi Freundlich sedangkan daya adsorpsi maksimum dari membran PEC kitosan pektin ditentukan dari kurva berdasarkan karakteristik membran yang diperoleh. Hasil penelitian menunjukkan bahwa adsorpsi zat warna azo jenis Remazol Black B terjadi pada kondisi optimum dengan pH 5, waktu 120 menit dan konsentrasi larutan zat warna azo jenis Remazol Black B 10 mg/L (62,75 %. Pola adsorpsi mengikuti pola adsorpsi isoterm Freundlich dengan daya adsorpsi maksimum 0,02 (mg/g. Untuk efisiensi desorpsi maksimal diperoleh pada larutan NaCl 1 M (11,17 % Kata Kunci: adsorpsi, membran polielektrolit kitosan pektin, Remazol Black B Abstract Azo dyes produced approximately 2-50% from dying process were thrown through effluent to the environment without any treatment. The objective of this research were to know the optimum condition of PEC chitosan pectin membrane using to adsorp Remazol Black B with various contact time (5-150 min, pH (5-9 and Remazol Black B concentration (5, 10, 15, 20, dan 25 mg/L. Adsorption charactheristic of Remazol Black B by PEC chitosan pectin membrane were determined by Langmuir and

  3. Enhanced performance of a quasi-solid-state dye-sensitized solar cell with aluminum nitride in its gel polymer electrolyte

    KAUST Repository

    Huang, Kuan-Chieh

    2011-08-01

    The effects of incorporation of aluminum nitride (AlN) in the gel polymer electrolyte (GPE) of a quasi-solid-state dye-sensitized solar cell (DSSC) were studied in terms of performance of the cell. The electrolyte, consisting of lithium iodide (LiI), iodine (I2), and 4-tert-butylpyridine (TBP) in 3-methoxypropionitrile (MPN), was solidified with poly(vinyidene fluoride-co-hexafluoro propylene) (PVDF-HFP). The 0.05, 0.1, 0.3, and 0.5 wt% of AlN were added to the electrolyte for this study. XRD analysis showed a reduction of crystallinity in the polymer PVDF-HFP for all the additions of AlN. The DSSC fabricated with a GPE containing 0.1 wt% AlN showed a short-circuit current density (JSC) and power-conversion efficiency (η) of 12.92±0.54 mA/cm2 and 5.27±0.23%, respectively, at 100 mW/cm2 illumination, in contrast to the corresponding values of 11.52±0.21 mA/cm2 and 4.75±0.08% for a cell without AlN. The increases both in JSC and in η of the promoted DSSC are attributed to the higher apparent diffusion coefficient of I- in its electrolyte (3.52×10-6 cm2/s), compared to that in the electrolyte without AlN of a DSSC (2.97×10-6 cm 2/s). At-rest stability of the quasi-solid-state DSSC with 0.1 wt% of AlN was found to decrease hardly by 5% and 7% at room temperature and at 40 °C, respectively, after 1000 h duration. The DSSC with a liquid electrolyte showed a decrease of about 40% at room temperature, while it virtually lost its performance in about 150 h at 40 °C. Explanations are further substantiated by means of electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and by porosity measurements. © 2010 Elsevier B.V.

  4. Room temperature solid-state synthesis of a conductive polymer for applications in stable I₂-free dye-sensitized solar cells.

    Science.gov (United States)

    Kim, Byeonggwan; Koh, Jong Kwan; Kim, Jeonghun; Chi, Won Seok; Kim, Jong Hak; Kim, Eunkyoung

    2012-11-01

    A solid-state polymerizable monomer, 2,5-dibromo-3,4-propylenedioxythiophene (DBProDOT), was synthesized at 25 °C to produce a conducting polymer, poly(3,4-propylenedioxythiophene) (PProDOT). Crystallographic studies revealed a short interplane distance between DBProDOT molecules, which was responsible for polymerization at low temperature with a lower activation energy and higher exothermic reaction than 2,5-dibromo-3,4-ethylenedioxythiophene (DBEDOT) or its derivatives. Upon solid-state polymerization (SSP) of DBProDOT at 25 °C, PProDOT was obtained in a self-doped state with tribromide ions and an electrical conductivity of 0.05 S cm⁻¹, which is considerably higher than that of chemically-polymerized PProDOT (2×10⁻⁶ S cm⁻¹). Solid-state ¹³C NMR spectroscopy and DFT calculations revealed polarons in PProDOT and a strong perturbation of carbon nuclei in thiophenes as a result of paramagnetic broadening. DBProDOT molecules deeply penetrated and polymerized to fill nanocrystalline TiO₂ pores with PProDOT, which functioned as a hole-transporting material (HTM) for I₂-free solid-state dye-sensitized solar cells (ssDSSCs). With the introduction of an organized mesoporous TiO₂ (OM-TiO₂) layer, the energy conversion efficiency reached 3.5 % at 100 mW cm⁻², which was quite stable up to at least 1500 h. The cell performance and stability was attributed to the high stability of PProDOT, with the high conductivity and improved interfacial contact of the electrode/HTM resulting in reduced interfacial resistance and enhanced electron lifetime. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Laser Dyes

    Indian Academy of Sciences (India)

    amplification or generation of coherent light waves in the UV,. VIS, and near IR region. .... ciency in most flashlamp pumped dye lasers. It is used as reference dye .... have led to superior laser dyes with increased photostabilities. For instance ...

  6. Degradation of Synthetic Dyes by Laccases – A Mini-Review

    Directory of Open Access Journals (Sweden)

    Legerská Barbora

    2016-06-01

    Full Text Available Laccases provide a promising future as a tool to be used in the field of biodegradation of synthetic dyes with different chemical structures. These enzymes are able to oxidize a wide range of phenolic substrates without the presence of additional co-factors. Laccases have been confirmed for their potential of synthetic dye degradation from wastewater and degradation products of these enzymatic reactions become less toxic than selected dyes. This study discusses the potential of laccase enzymes as agents for laccase-catalyzed degradation in terms of biodegradation efficiency of synthetic dyes, specifically: azo dyes, triphenylmethane, indigo and anthraquinone dyes. Review also summarizes the laccase-catalyzed degradation mechanisms of the selected synthetic dyes, as well as the degradation products and the toxicity of the dyes and their degradation products.

  7. Adsorption of a Textile Dye on Commercial Activated Carbon: A Simple Experiment to Explore the Role of Surface Chemistry and Ionic Strength

    Science.gov (United States)

    Martins, Angela; Nunes, Nelson

    2015-01-01

    In this study, an adsorption experiment is proposed using commercial activated carbon as adsorbent and a textile azo dye, Mordant Blue-9, as adsorbate. The surface chemistry of the activated carbon is changed through a simple oxidation treatment and the ionic strength of the dye solution is also modified, simulating distinct conditions of water…

  8. Genetic damage induced by a food coloring dye (sunset yellow) on meristematic cells of Brassica campestris L.

    Science.gov (United States)

    Dwivedi, Kshama; Kumar, Girjesh

    2015-01-01

    We have performed the present piece of work to evaluate the effect of synthetic food coloring azo dye (sunset yellow) on actively dividing root tip cells of Brassica campestris L. Three doses of azo dye were administered for the treatment of actively dividing root tip cells, namely, 1%, 3%, and 5%, for 6-hour duration along with control. Mitotic analysis clearly revealed the azo dye induced endpoint deviation like reduction in the frequency of normal divisions in a dose dependent manner. Mitotic divisions in the control sets were found to be perfectly normal while dose based reduction in MI was registered in the treated sets. Azo dye has induced several chromosomal aberrations (genotoxic effect) at various stages of cell cycle such as stickiness of chromosomes, micronuclei formation, precocious migration of chromosome, unorientation, forward movement of chromosome, laggards, and chromatin bridge. Among all, stickiness of chromosomes was present in the highest frequency followed by partial genome elimination as micronuclei. The present study suggests that extensive use of synthetic dye should be forbidden due to genotoxic and cytotoxic impacts on living cells. Thus, there is an urgent need to assess potential hazardous effects of these dyes on other test systems like human and nonhuman biota for better scrutiny.

  9. Degradation of environment pollutant dyes using phytosynthesized metal nanocatalysts

    Science.gov (United States)

    MeenaKumari, M.; Philip, Daizy

    2015-01-01

    We present for the first time biogenic reduction and stabilization of gold and silver ions at room temperature using fruit juice of Punica granatum. The formation, morphology and crystalline structure of the synthesized nanoparticles are determined using UV-Visible, XRD and TEM. An attempt to reveal the partial role of phenolic hydroxyls in the reduction of Au3+ and Ag+ is done through FTIR analysis. The synthesized nanoparticles are used as potential catalysts in the degradation of a cationic phenothiazine dye, an anionic mono azo dye and a cationic fluorescent dye. The calculated values of percentage removal of dyes and the rate constants from pseudo first order kinetic data fit give a comparative study on degradation of organic dyes in presence of prepared gold and silver nanoparticles.

  10. The structural and electro-optical characteristics of AZO/Cr:Cu/AZO transparent conductive film

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Tien-Chai [Department of Electrical Engineering, Kun Shan University, No. 195, Kun-Da Road, Yung-Kang Dist., Tainan 71003, Taiwan, ROC (China); Huang, Wen-Chang, E-mail: wchuang@mail.ksu.edu.tw [Department of Electro-Optical Engineering, Kun Shan University, No. 195, Kun-Da Road, Yung-Kang Dist., Tainan 71003, Taiwan, ROC (China); Tsai, Fu-Chun [Department of Electro-Optical Engineering, Kun Shan University, No. 195, Kun-Da Road, Yung-Kang Dist., Tainan 71003, Taiwan, ROC (China)

    2015-08-31

    A novel triple-layered transparent conductive film, AZO/Cr:Cu/AZO (ACCA), was presented in the paper. The structural and electro-optical properties of the ACCA film were discussed. The thickness of the middle metal layer was constant and those of the AZO layers were varied. The ACCA film shows an obvious ZnO (002) c-axis preferential growth. No diffraction peaks related to Cr and Cu were observed through x-ray diffraction analysis. The middle Cr:Cu layer showed a thickness of 8.16 nm with a continuous and amorphous structure by the observation of a high-resolution transmission electron microscopy (HR-TEM). For the electro-optical characteristic, a best figure of merit (FOM) value of 3.54 × 10{sup −3} Ω{sup −1} with a corresponding transmittance of 85% was obtained at the thickness of 116 nm of ACCA film. The high FOM value of the film is due to the improvement of conductivity and small sacrifices of transparency. - Highlights: • A novel triple-layered transparent conductive film, AZO/Cr:Cu/AZO is developed. • Chromium is added to copper to reduce the oxidation–reduction reaction. • The film has a FOM of 3.54 × 10{sup −3} Ω{sup −1} with a corresponding transmittance of 85%. • The Cr:Cu layer shows a continuous and amorphous structure.

  11. The structural and electro-optical characteristics of AZO/Cr:Cu/AZO transparent conductive film

    International Nuclear Information System (INIS)

    Lin, Tien-Chai; Huang, Wen-Chang; Tsai, Fu-Chun

    2015-01-01

    A novel triple-layered transparent conductive film, AZO/Cr:Cu/AZO (ACCA), was presented in the paper. The structural and electro-optical properties of the ACCA film were discussed. The thickness of the middle metal layer was constant and those of the AZO layers were varied. The ACCA film shows an obvious ZnO (002) c-axis preferential growth. No diffraction peaks related to Cr and Cu were observed through x-ray diffraction analysis. The middle Cr:Cu layer showed a thickness of 8.16 nm with a continuous and amorphous structure by the observation of a high-resolution transmission electron microscopy (HR-TEM). For the electro-optical characteristic, a best figure of merit (FOM) value of 3.54 × 10 −3 Ω −1 with a corresponding transmittance of 85% was obtained at the thickness of 116 nm of ACCA film. The high FOM value of the film is due to the improvement of conductivity and small sacrifices of transparency. - Highlights: • A novel triple-layered transparent conductive film, AZO/Cr:Cu/AZO is developed. • Chromium is added to copper to reduce the oxidation–reduction reaction. • The film has a FOM of 3.54 × 10 −3 Ω −1 with a corresponding transmittance of 85%. • The Cr:Cu layer shows a continuous and amorphous structure

  12. Panchromatic response composed of hybrid visible-light absorbing polymers and near-IR absorbing dyes for nanocrystalline TiO{sub 2}-based solid-state solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hyo Joong; Graetzel, Michael; Nazeeruddin, Md. Khaja [Laboratory for Photonics and Interfaces, Institute of Chemical Sciences and Engineering, School of Basic Sciences, Swiss Federal Institute of Technology, CH-1015 Lausanne (Switzerland); Leventis, Henry C.; Haque, Saif A. [Department of Chemistry, Imperial College of Science Technology and Medicine, London SW72AZ (United Kingdom); Torres, Tomas [Departamento de Quimica Organica, Universidad Autonoma de Madrid (UAM), 28049 Madrid (Spain)

    2011-01-01

    In pursuit of panchromatic sensitizers for mesoporous TiO{sub 2}-based solid-state solar cells, a near-IR absorbing zinc phthalocyanine dye (coded TT1) was firstly adsorbed over relatively thin ({proportional_to}1 {mu}m) TiO{sub 2} mesoporous films and then a visible-light absorbing polymer [regioregular poly(3-hexylthiophene), P3HT] was incorporated into the mesopores as both a second sensitizer and a solid hole conductor. After optimizing some experimental parameters, these hybrid solid-state cells exhibited a clear panchromatic response, and an overall conversion efficiency of around 1% at full sun intensity. (author)

  13. Synthesis and Investigation Absorption Features of Some Novel Hetarylazo Dyes Derived from Calix[4]resorcinarene

    Directory of Open Access Journals (Sweden)

    İzzet Şener

    2013-12-01

    Full Text Available In this study, several derivatives of amines were diazotized and coupled with 3-aminocrotonitrile to give 2-arylhydrazon-3-ketiminocrotononitrile. The synthesized components were then refluxed with hydrazine hydrate in ethanol to give a series of dyes 5-amino-4-arylazo-3-ethyl-1'H-Pyrazole. The synthesized dyes were diazotised and coupled with resorcinarene, which was obtained from condensation of between resorcinol and acetaldehyde, to give a new synthesis of azo dyes based on resorcinarene. The structures of synthesized dyes based on resorcinarene were characterized by spectral methods. The effect of varying solvents, acid and base upon the absorption spectra of resultant dyes has been investigated. Key words: Resorcinarene, Azo Dyes, Absorption Spectra, Solvent Effect, Acid-Base Effect Rezorsinaren Bazlı Azo Boyarmaddelerin Sentezi ve Absorpsiyon Özelliklerinin İncelenmesi Özet: Bu çalışmada, çeşitli amin türevleri diazolanmış ve 3-aminokrotonitril ile kenetlenerek 2-arilhidrazon-3-ketiminokrotononitril bileşikleri elde edilmiştir. Elde edilen bileşikler, hidrazinhidrat ile etanol içerisinde reflaks edilerek bir seri 5-amino-4-arilazo-3-metil-1'H-pirazol boyaları elde edilmiştir. Elde edilen boyalar diazonlarak rezorsinol ve asetaldehit arasındaki kondenzasyondan elde edilen rezorsinaren bileşiği ile kenetlenmiş ve rezorsinaren bazlı azo boyarmaddeler sentezlenmiştir. Sentezlenen rezorsinaren bazlı azoboyarmaddelerin yapıları spektrofotometrik yöntemler kullanılarak incelendi. Sentezlenen boyarmaddelerin görünür bölge absorpsiyon spektrumları üzerine değişik çözücü, asit ve baz etkileri incelendi. Anahtar kelimeler: Rezorsiaren, Azo Boyarmadde, Absorpsiyon Spektrumu, Çözücü Etkisi, Asit-Baz Etkisi

  14. Voltammetric determination of zirconium using azo compounds

    International Nuclear Information System (INIS)

    Orshulyak, O.O.; Levitskaya, G.D.

    2008-01-01

    The optimum conditions for zirconium complexation with azo compounds are found. The applicability of Eriochrome Red B, Calcon, and Calcion to the voltammetric determination of zirconium, total Zr(IV) and Hf(IV), and Zr(IV) in the presence of Zn(II), Cu(II), Cd(II), Ni(II), or Ti(IV) is demonstrated. The developed procedures are used to determine zirconium in a terbium alloy and in an alloy for airplane wheel drums [ru

  15. Optical sensors from electrohydrodynamic jetted polymer fiber resonators

    DEFF Research Database (Denmark)

    Laye, Fabrice; Kraemmer, Sarah; Castillo, Alejandro

    2016-01-01

    Electrohydrodynamic jetting is used to manufacture dye-doped polymer fiber resonators. We present comb-like laser emission from different polymer/dye combinations and report the use of these structures as sensitive detection of ethanol and methanol.......Electrohydrodynamic jetting is used to manufacture dye-doped polymer fiber resonators. We present comb-like laser emission from different polymer/dye combinations and report the use of these structures as sensitive detection of ethanol and methanol....

  16. A solid-state dye-sensitized solar cell based on a novel ionic liquid gel and ZnO nanoparticles on a flexible polymer substrate

    Energy Technology Data Exchange (ETDEWEB)

    Wei Di; Ryhanen, Tapani [Nokia Research Centre c/o Nanoscience Centre, University of Cambridge, 11 JJ Thomson Avenue, CB3 0FF, Cambridge (United Kingdom); Unalan, Husnu Emrah; Amaratunga, Gehan [Centre of Advanced Photonics and Electronics, Department of Engineering, University of Cambridge, 9 JJ Thomson Avenue, CB3 0FA, Cambridge (United Kingdom); Han Dongxue; Zhang Qixian; Niu Li [Changchun Institute of Applied Chemistry, Chinese Academy of Science, 130000 Changchun (China)], E-mail: di.wei@nokia.com

    2008-10-22

    This paper describes a new strategy to make a full solid-state, flexible, dye-sensitized solar cell (DSSC) based on novel ionic liquid gel, organic dye, ZnO nanoparticles and carbon nanotube (CNT) thin film stamped onto a polyethylene terephthalate (PET) substrate. The CNTs serve both as the charge collector and as scaffolds for the growth of ZnO nanoparticles, where the black dye molecules are anchored. It opens up the possibility of developing a continuous roll to roll processing for THE mass production of DSSCs.

  17. Modeling fiber Bragg grating device networks in photomechanical polymer optical fibers

    Science.gov (United States)

    Lanska, Joseph T.; Kuzyk, Mark G.; Sullivan, Dennis M.

    2015-09-01

    We report on the modeling of fiber Bragg grating (FBG) networks in poly(methyl methacrylate) (PMMA) polymer fibers doped with azo dyes. Our target is the development of Photomechanical Optical Devices (PODs), comprised of two FBGs in series, separated by a Fabry-Perot cavity of photomechanical material. PODs exhibit photomechanical multi-stability, with the capacity to access multiple length states for a fixed input intensity when a mechanical shock is applied. Using finite-difference time-domain (FDTD) numerical methods, we modeled the photomechanical response of both Fabry-Perot and Bragg-type PODs in a single polymer optical fiber. The polymer fiber was modeled as an instantaneous Kerr-type nonlinear χ(3) material. Our model correctly predicts the essential optical features of FBGs as well as the photomechanical multi-stability of nonlinear Fabry-Perot cavity-based PODs. Networks of PODs may provide a framework for smart shape-shifting materials and fast optical computation where the decision process is distributed over the entire network. In addition, a POD can act as memory, and its response can depend on input history. Our models inform and will accelerate targeted development of novel Bragg grating-based polymer fiber device networks for a variety of applications in optical computing and smart materials.

  18. Phycoremediation of industrial wastewater containing azo compounds

    OpenAIRE

    Parin D. Shah; Dipti Galani; M S. Rao

    2000-01-01

    This paper summarizes the state-of-the-art biological wastewater treatment technique that uses eukaryotic microalgae as well as several prokaryotic photosynthetic cyanobacteria. Micro algae are known to remove dyes by bioadsorption (sorption of dye molecules over the surface of algal cells), biodegradation and bioconversion (diffusion of dye molecules into the algal cells and subsequent conversion). This paper mainly focuses on biodegradation abilities of microalgae for t...

  19. PHYSICO-CHEMICAL STUDIES OF DISAZO DYES DERIVED ...

    African Journals Online (AJOL)

    DJFLEX

    with disazo disperse dyes on synthetic polymer-fibres. (Venkataraman, 1974; Otutu et al., 2008). In this present study, the physico-chemical studies of disazo dyes derived from p-aminophenol recently prepared by our research group is described. We also described the kinetics of the dyes on nylon 6 fibre. In another study.

  20. Electrical circuit model of ITO/AZO/Ge photodetector

    Directory of Open Access Journals (Sweden)

    Malkeshkumar Patel

    2017-10-01

    Full Text Available In this data article, ITO/AZO/Ge photodetector was investigated for electrical circuit model. Due to the double (ITO and AZO transparent metal-oxide films (DOI:10.1016/j.mssp.2016.03.007 (Yun et al., 2016 [1], the Ge heterojunction device has a better interface quality due to the AZO layer with a low electrical resistance due to the ITO layer (Yun et al., 2015 [2]. The electrical and interfacial benefitted ITO/AZO/Ge heterojunction shows the quality Schottky junction. In order to investigate the device, the ITO/AZO/Ge heterojunction was analyzed by R–C circuit model using the impedance spectroscopy.

  1. Preparation and Properties of Flexible AZO@C Nanofibers

    Directory of Open Access Journals (Sweden)

    MA Hui

    2018-01-01

    Full Text Available A new type of environmental-friendly flexible nanofibers of aluminum doped zinc oxide (AZO coated carbon (AZO@C was successfully prepared by using polyvinyl alcohol (PVA as raw materials. The as-spun PVA nanofibers were prepared via electrospinning and its water resistance was greatly improved after heat-treatment. Then, the PVA nanofibers with a layer of zinc aluminum hydroxide on the surface were synthesized by hydrothermal method. Thereafter, new AZO@C composite nanofibers was produced after sintering at 500℃ to the carbonization of PVA nanofibers and the dehydration of zinc aluminum hydroxide to form AZO nanoparticles. The structure and properties of the samples were characterized by Fourier-transform infrared spectrometer (FT-IR, thermal gravimetric analyzer (TGA and scanning electron microscope (SEM. The average diameter of the AZO@C nanofibers is (320±45nm. The photocatalytic property of the resultant composite fibers is demonstrated by degrading methyl orange under solar light.

  2. Phytoremediation in education: textile dye teaching experiments.

    Science.gov (United States)

    Ibbini, Jwan H; Davis, Lawrence C; Erickson, Larry E

    2009-07-01

    Phytoremediation, the use of plants to clean up contaminated soil and water, has a wide range of applications and advantages, and can be extended to scientific education. Phytoremediation of textile dyes can be used as a scientific experiment or demonstration in teaching laboratories of middle school, high school and college students. In the experiments that we developed, students were involved in a hands-on activity where they were able to learn about phytoremediation concepts. Experiments were set up with 20-40 mg L(-1) dye solutions of different colors. Students can be involved in the set up process and may be involved in the experimental design. In its simplest forms, they use two-week-old sunflower seedlings and place them into a test tube of known volume of dye solution. Color change and/or dye disappearance can be monitored by visual comparison or with a spectrophotometer. Intensity and extent of the lab work depends on student's educational level, and time constraints. Among the many dyes tested, Evan's Blue proved to be the most readily decolorized azo dye. Results could be observed within 1-2 hours. From our experience, dye phytoremediation experiments are suitable and easy to understand by both college and middle school students. These experiments help visual learners, as students compare the color of the dye solution before and after the plant application. In general, simple phytoremediation experiments of this kind can be introduced in many classes including biology, biochemistry and ecological engineering. This paper presents success stories of teaching phytoremediation to middle school and college students.

  3. Efficient holographic recording in novel azo-containing polymer

    Czech Academy of Sciences Publication Activity Database

    Mysliwiec, J.; Miniewicz, A.; Nešpůrek, Stanislav; Studenovský, Martin; Sedláková, Zdeňka

    2007-01-01

    Roč. 29, č. 12 (2007), s. 1756-1762 ISSN 0925-3467 R&D Projects: GA AV ČR IAA4112401; GA MŠk OC 138 Institutional research plan: CEZ:AV0Z40500505 Keywords : azopolymers * dynamic holography * photochromism Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.519, year: 2007

  4. Dataset on analysis of dyeing property of natural dye from Thespesia populnea bark on different fabrics

    Directory of Open Access Journals (Sweden)

    Kuchekar Mohini

    2018-02-01

    Full Text Available The natural dyes separated from plants are of gaining interest as substitutes for synthetic dyes in food and cosmetics. Thespesia populnea (T. populnea is widely grown plant and used in the treatment of various diseases. This study was aimed to separate natural dye from T. populnea bark and analysis of its dyeing property on different fabrics. In this investigation pharmacognostic study was carried out. The pharmacognostic study includes morphological study, microscopical examination, proximate analysis along with the phytochemical study. The dyeing of different fabric was done with a natural dye extracted from T. populnea bark. The fabrics like cotton, butter crep, polymer, chiken, lone, ulene and tarakasa were dye with plant extract. The various evaluation parameters were studied. It includes effect of washing with water, effect of soap, effect of sunlight, effect of alum, effect of Cupric sulphate, microscopical study of fabrics and visual analysis of dyeing by common people were studied. In results, natural dye isolated from T. populnea bark could be used for dyeing fabrics with good fastness properties. The studies reveals that, the dyeing property of fabrics after washing with water and soap, exposed to sunlight does not get affected. It was observed that cotton and tarakasa stains better as compared with other fabrics. It was concluded that the ethanolic extract having good dyeing property. Keywords: Plant, Thespesia populnea, Bark, Natural dye, Fabrics

  5. Studies on Synthesis and Dyeing Preformance of Acid Dyes Based on 4,7-Dihydroxy-3,8-di-α-naphthylazo-1,10-phenanthroline-2,9-Dione

    Directory of Open Access Journals (Sweden)

    B. V. Patel

    2007-01-01

    Full Text Available Some new azo acid dyes were prepared by coupling various diazotized acid components such as anthranilic acid, sulphanilic acid, laurentacid, peri acid, tobias acid, H-acid, J-acid, gamma acid, sulphotobias acid,4-aminotoluiene-3-sulphonic acid, 5-sulpho- anthranilic acid, 2-naphthylamine-3,6,8-trisulphonic acid, bronner acid, metanilic acid and cleve acid with 4,7-dihydroxy-3,8-di-α-naphthylazo-1,10-phenanthroline-2,9-dione. The dyes were characterized by elemental, IR and TLC analyses. Their dyeing performance as acid dyes has been assessed on viscose rayon, wool and cotton fibres.

  6. Micro-Cavity Fluidic Dye Laser

    DEFF Research Database (Denmark)

    Helbo, Bjarne; Kristensen, Anders; Menon, Aric Kumaran

    2003-01-01

    We have successfully designed, fabricated and characterized a micro-cavity fluidic dye laser with metallic mirrors, which can be integrated with polymer based lab-on-a-chip microsystems without further processing steps. A simple rate-equation model is used to predict the average pumping power...... threshold for lasing as function of cavity-mirror reflectance, laser dye concentration and cavity length. The laser device is characterized using the laser dye Rhodamine 6G dissolved in ethanol. Lasing is observed, and the influence of dye concentration is investigated....

  7. Syntheses, structures, electrochemistry and catalytic oxidation degradation of organic dyes of two new coordination polymers derived from Cu(II) and Mn(II) and 1-(tetrazo-5-yl)-4-(triazo-1-yl)benzene

    Energy Technology Data Exchange (ETDEWEB)

    Song, Ming; Mu, Bao; Huang, Ru-Dan, E-mail: huangrd@bit.edu.cn

    2017-02-15

    Two new coordination polymers (CPs), namely, [Cu{sub 2}(ttbz)(H{sub 2}btc){sub 2}(OH)]{sub n} (1) and [Mn(ttbz){sub 2}(H{sub 2}O){sub 2}]{sub n} (2) (Httbz =1-(tetrazo-5-yl)-4-(triazo-1-yl)benzene, H{sub 3}btc =1,3,5-benzenetricarboxylic acid), have been hydrothermally synthesized and structurally characterized. Complex 1 exhibits a (3,5,5,5)-connected 2D layer with a Schläfli symbol of (3·4{sup 2})(3·4{sup 4}0.5{sup 2}0.6{sup 3})(3{sup 2}0.4{sup 4}0.5{sup 2}0.6{sup 2})(3{sup 2}0.4{sup 4}0.5{sup 3}0.6), in which the ttbz{sup -} ligand can be described as μ{sub 5}-bridge, linking Cu(II) ions into a 2D layer and H{sub 2}btc{sup -} ions play a supporting role in complex 1. The ttbz{sup -} ligand in complex 2 represents the bridging coordination mode, connecting two Mn(II) ions to form the infinite 1D zigzag chains, respectively, which are further connected by two different types of hydrogen bonds to form a 3D supramolecular. Furthermore, catalytic oxidation activities toward organic dyes and electrochemical behaviors of the title complexes have been investigated at room temperature in aqueous solutions, indicating these complexes may be applicable to color removal in a textile wastewater stream and practical applications in areas of electrocatalytic reduction toward nitrite, respectively. - Graphical abstract: Two new coordination polymers based on different structural characteristics have been hydrothermally synthesized by the mixed ligands. The catalytic oxidation activities toward organic dyes and electrochemical behaviors of the title complexes have been investigated. - Highlights: • The organic ligand containing the tetrazolyl group and triazolyl group with some advantages has been used. • Two new coordination polymers with different structural characteristics has been discussed in detail. • Catalytic oxidation activities toward organic dyes and electrochemical behaviors of the title complexes have been investigated.

  8. Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes

    Directory of Open Access Journals (Sweden)

    Alimmari Adel

    2012-07-01

    Full Text Available Abstract Background A series of some novel arylazo pyridone dyes was synthesized from the corresponding diazonium salt and 6-hydroxy-4-phenyl-3-cyano-2-pyridone using a classical reaction for the synthesis of the azo compounds. Results The structure of the dyes was confirmed by UV-vis, FT-IR, 1H NMR and 13C NMR spectroscopic techniques and elemental analysis. The solvatochromic behavior of the dyes was evaluated with respect to their visible absorption properties in various solvents. Conclusions The azo-hydrazone tautomeric equilibration was found to depend on the substituents as well as on the solvent. The geometry data of the investigated dyes were obtained using DFT quantum-chemical calculations. The obtained calculational results are in very good agreement with the experimental data.

  9. Acid Blue dyes in polypyrrole synthesis: the control of polymer morphology at nanoscale in the promotion of high conductivity and the reduction of cytotoxicity

    Czech Academy of Sciences Publication Activity Database

    Bober, Patrycja; Li, Yu; Acharya, Udit; Panthi, Yadu Ram; Pfleger, Jiří; Humpolíček, P.; Trchová, Miroslava; Stejskal, Jaroslav

    2018-01-01

    Roč. 237, March (2018), s. 40-49 ISSN 0379-6779 R&D Projects: GA ČR(CZ) GA17-04109S Institutional support: RVO:61389013 Keywords : Acid Blue * conducting polymer * conductivity Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 2.435, year: 2016

  10. New azo coupling reactions for visible spectrophotometric determination of salbutamol in bulk and pharmaceutical preparations

    International Nuclear Information System (INIS)

    Dhahir, S. A.

    2011-01-01

    The purpose of the present study was to develop a new, simple, cheap, fast, accurate, and sensitive colorimetric methods that can be used for the determination of salbutamol sulphate drug in pure from as well as in pharmaceutical formulations. The method is based on the reaction 2-chloro-4-nitroaniline with nitrite in acid medium to form diazonium ion, which is coupled with of salbutamol in basic medium to form azo dyes, showing yellow color and absorption maxima at 463 nm. Beer's law is obeyed in the concentration of 4-48μg/ml. The molar absorptivity and san dell's sensitivity are 5.27x103 L mole-1 cm-1, 0.015 μgcm-2, respectively. The optimum reaction conditions and other analytical parameters were evaluated. (author).

  11. Optofluidic third order distributed feedback dye laser

    DEFF Research Database (Denmark)

    Gersborg-Hansen, Morten; Kristensen, Anders

    2006-01-01

    which has a refractive index lower than that of the polymer. In combination with a third order DFB grating, formed by the array of nanofluidic channels, this yields a low threshold for lasing. The laser is straightforward to integrate on lab-on-a-chip microsystems where coherent, tunable light......This letter describes the design and operation of a polymer-based third order distributed feedback (DFB) microfluidic dye laser. The device relies on light confinement in a nanostructured polymer film where an array of nanofluidic channels is filled by capillary action with a liquid dye solution...

  12. A Lipophilic IR-780 Dye-Encapsulated Zwitterionic Polymer-Lipid Micellar Nanoparticle for Enhanced Photothermal Therapy and NIR-Based Fluorescence Imaging in a Cervical Tumor Mouse Model

    Directory of Open Access Journals (Sweden)

    Santhosh Kalash Rajendrakumar

    2018-04-01

    Full Text Available To prolong blood circulation and avoid the triggering of immune responses, nanoparticles in the bloodstream require conjugation with polyethylene glycol (PEG. However, PEGylation hinders the interaction between the nanoparticles and the tumor cells and therefore limits the applications of PEGylated nanoparticles for therapeutic drug delivery. To overcome this limitation, zwitterionic materials can be used to enhance the systemic blood circulation and tumor-specific delivery of hydrophobic agents such as IR-780 iodide dye for photothermal therapy. Herein, we developed micellar nanoparticles using the amphiphilic homopolymer poly(12-(methacryloyloxydodecyl phosphorylcholine (PCB-lipid synthesized via reversible addition–fragmentation chain transfer (RAFT polymerization. The PCB-lipid can self-assemble into micelles and encapsulate IR-780 dye (PCB-lipid–IR-780. Our results demonstrated that PCB-lipid–IR-780 nanoparticle (NP exhibited low cytotoxicity and remarkable photothermal cytotoxicity to cervical cancer cells (TC-1 upon near-infrared (NIR laser irradiation. The biodistribution of PCB-lipid–IR-780 showed higher accumulation of PCB-lipid–IR-780 than that of free IR-780 in the TC-1 tumor. Furthermore, following NIR laser irradiation of the tumor region, the PCB-lipid–IR-780 accumulated in the tumor facilitated enhanced tumor ablation and subsequent tumor regression in the TC-1 xenograft model. Hence, these zwitterionic polymer-lipid hybrid micellar nanoparticles show great potential for cancer theranostics and might be beneficial for clinical applications.

  13. Mycoremediation of congo red dye by filamentous fungi.

    Science.gov (United States)

    Bhattacharya, Sourav; Das, Arijit; G, Mangai; K, Vignesh; J, Sangeetha

    2011-10-01

    Azo, anthroquinone and triphenylmethane dyes are the major classes of synthetic colourants, which are difficult to degrade and have received considerable attention. Congo red, a diazo dye, is considered as a xenobiotic compound, and is recalcitrant to biodegradative processes. Nevertheless, during the last few years it has been demonstrated that several fungi, under certain environmental conditions, are able to transfer azo dyes to non toxic products using laccases. The aim of this work was to study the factors influencing mycoremediation of Congo red. Several basidiomycetes and deuteromycetes species were tested for the decolourisation of Congo red (0.05 g/l) in a semi synthetic broth at static and shaking conditions. Poor decolourisation was observed when the dye acted as the sole source of nitrogen, whereas semi synthetic broth supplemented with fertilizer resulted in better decolourisation. Decolourisation of Congo red was checked in the presence of salts of heavy metals such as mercuric chloride, lead acetate and zinc sulphate. Decolourisation parameters such as temperature, pH, and rpm were optimized and the decolourisation obtained at optimized conditions varied between 29.25- 97.28% at static condition and 82.1- 100% at shaking condition. Sodium dodecyl sulphate polyacrylamide gel electrophoretic analysis revealed bands with molecular weights ranging between 66.5 to 71 kDa, a characteristic of the fungal laccases. High efficiency decolourisation of Congo red makes these fungal forms a promising choice in biological treatment of waste water containing Congo red.

  14. Mycoremediation of Congo red dye by filamentous fungi

    Directory of Open Access Journals (Sweden)

    Sourav Bhattacharya

    2011-12-01

    Full Text Available Azo, anthroquinone and triphenylmethane dyes are the major classes of synthetic colourants, which are difficult to degrade and have received considerable attention. Congo red, a diazo dye, is considered as a xenobiotic compound, and is recalcitrant to biodegradative processes. Nevertheless, during the last few years it has been demonstrated that several fungi, under certain environmental conditions, are able to transfer azo dyes to non toxic products using laccases. The aim of this work was to study the factors influencing mycoremediation of Congo red. Several basidiomycetes and deuteromycetes species were tested for the decolourisation of Congo red (0.05 g/l in a semi synthetic broth at static and shaking conditions. Poor decolourisation was observed when the dye acted as the sole source of nitrogen, whereas semi synthetic broth supplemented with fertilizer resulted in better decolourisation. Decolourisation of Congo red was checked in the presence of salts of heavy metals such as mercuric chloride, lead acetate and zinc sulphate. Decolourisation parameters such as temperature, pH, and rpm were optimized and the decolourisation obtained at optimized conditions varied between 29.25- 97.28% at static condition and 82.1- 100% at shaking condition. Sodium dodecyl sulphate polyacrylamide gel electrophoretic analysis revealed bands with molecular weights ranging between 66.5 to 71 kDa, a characteristic of the fungal laccases. High efficiency decolourisation of Congo red makes these fungal forms a promising choice in biological treatment of waste water containing Congo red.

  15. Synthesis, spectroscopic, and molecular structure characterizations of some azo derivatives of 2-hydroxyacetophenone

    Science.gov (United States)

    Albayrak, Çiğdem; Gümrükçüoğlu, İsmail E.; Odabaşoğlu, Mustafa; İskeleli, Nazan Ocak; Ağar, Erbil

    2009-08-01

    Some novel azo compounds were prepared by the reaction of 2-hydroxyacetophenone with aniline and its substituted derivatives. The structures of synthesized azo compounds were determined by IR, UV-Vis, 1H NMR and 13C NMR spectroscopic techniques and the structures of some of these compounds were also determined by X-ray diffraction studies. Structural analysis using IR in solid state shows that the azo form is favoured in the azo compounds whereas UV-Vis analysis of the azo compounds in solution has shown that there is a azo and ionic form. The azo compounds in the basic solvents dimethylformamide (DMF) and dimethylsulfoxide (DMSO) are both azo and ionic form while these compounds in ethyl alcohol (EtOH) and chloroform (CHCl 3) are only azo form.

  16. Optimization of AZO films prepared on flexible substrates

    Indian Academy of Sciences (India)

    Administrator

    grey relational analysis, the optimization of these deposition process parameters for AZO thin films with multiple characteristics ... bias voltage, annealing temperature and plasma treatment deposition time (Pei et ... water and dried in nitrogen.

  17. Ion irradiation of