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Sample records for degrades methyl t-butyl

  1. Biodegradation of ethyl t-butyl ether (ETBE), methyl t-butyl ether (MTBE) and t-amyl methyl ether (TAME) by Gordonia terrae.

    Science.gov (United States)

    Hernandez-Perez, G; Fayolle, F; Vandecasteele, J P

    2001-01-01

    Gordonia terrae strain IFP 2001 was selected from activated sludge for its capacity to grow on ethyl t-butyl ether (ETBE) as sole carbon and energy source. ETBE was stoichiometrically degraded to t-butyl alcohol (TBA) and the activity was inducible. A constitutive strain, G. terrae IFP 2007, derived from strain IFP 2001, was also selected. Methyl t-butyl ether (MTBE) and t-amyl methyl ether (TAME) were not used as carbon and energy sources by the two strains, but cometabolic degradation of MTBE and TAME was demonstrated, to TBA and t-amyl alcohol (TAA) respectively, in the presence of a carbon source such as ethanol. No two-carbon compound was detected during growth on ETBE, but formate was produced during cometabolic degradation of MTBE or TAME. A monooxygenase was involved in the degradation of ethers, because no degradation of ETBE was observed under anaerobic conditions and the presence of a cytochrome P-450 was demonstrated in G. terrae IFP 2001 after induction by cultivation on ETBE.

  2. Liquid/air partition coefficients of methyl and ethyl T-butyl ethers, T-amyl methyl ether, and T-butyl alcohol.

    Science.gov (United States)

    Nihlen, A; Lof, A; Johanson, G

    1995-01-01

    Partition coefficients are essential to a description of the uptake and distribution of volatile substances in humans and in the development of physiologically based pharmacokinetic models. Liquid/air partition coefficients (lambda) of three ethers, methyl t-butyl ether (MTBE), ethyl t-butyl ether (ETBE), and t-amyl methyl ether (TAME) were determined in vitro by head space-gas chromatography. These ethers, and especially MTBE, are used in unleaded gasoline to enhance the oxygen and octane content, and to reduce the output of carbon monoxide during combustion. Partition coefficients of t-butyl alcohol (TBA), a metabolite of MTBE, were determined also. The liquids tested were fresh human blood, water (physiological saline), and olive oil. The (lambda)blood/air values were: 17.7 (95% confidence interval 17.0-18.4) for MTBE; 11.7 (11.3-12.1) for ETBE; and 17.9 (17.3-18.5) for TAME. Corresponding (lambda)water/air values were 15.2 (14.9-15.5), 8.39 (8.19-8.59), and 11.9 (11.7-12.1). The ethers have a higher affinity for oil, the values for (lambda)oil/air being 120 (114-125), 190 (183-197), and 337 (320-354), respectively. As expected, the (lambda)blood/air and (lambda)water/air for TBA were much higher than for the ethers, 462 (440-484) and 603 (590-617), respectively. The (lambda)oil/air was 168 (161-174) for TBA. The interindividual variability of the (lambda)blood/air (10 subjects) was calculated as the coefficient of variation, and estimated as: 14% for MTBE, 20% for ETBE, 20% for TAME, and 30% for TBA. No significant difference was seen in the (lambda)blood/air between the sexes.

  3. Influence of Temperature on Thermodynamic Properties of Methyl t-Butyl Ether (MTBE) + Gasoline Additives

    Science.gov (United States)

    Gonzalez-Olmos, R.; Iglesias, M.; Goenaga, J. M.; Resa, J. M.

    2007-08-01

    The densities and sound speeds of binary mixtures of methyl tert-butyl ether (MTBE) + (benzene, toluene, ethylbenzene, isooctane, tert-butyl alcohol) have been measured at temperatures from 288.15 to 323.15 K and at atmospheric pressure over the complete concentration range. The experimental excess volumes and deviations of isentropic compressibility were calculated. The deviation of isentropic compressibility data have been analyzed in terms of different theoretical models; adequate agreement between the experimental and predicted values is obtained. The data from this study improve the data situation related to gasoline additives and help to understand the MTBE volumetric and acoustic behavior for various chemical systems.

  4. Solid state {sup 1}H spin-lattice relaxation and isolated-molecule and cluster electronic structure calculations in organic molecular solids: The relationship between structure and methyl group and t-butyl group rotation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xianlong, E-mail: WangXianlong@uestc.edu.cn, E-mail: pbeckman@brynmawr.edu [Key Laboratory for NeuroInformation of Ministry of Education, School of Life Science and Technology, University of Electronic Science and Technology of China, 4 North Jianshe Rd., 2nd Section, Chengdu 610054 (China); Mallory, Frank B. [Department of Chemistry, Bryn Mawr College, 101 North Merion Ave., Bryn Mawr, Pennsylvania 19010-2899 (United States); Mallory, Clelia W. [Department of Chemistry, Bryn Mawr College, 101 North Merion Ave., Bryn Mawr, Pennsylvania 19010-2899 (United States); Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323 (United States); Odhner, Hosanna R.; Beckmann, Peter A., E-mail: WangXianlong@uestc.edu.cn, E-mail: pbeckman@brynmawr.edu [Department of Physics, Bryn Mawr College, 101 North Merion Ave., Bryn Mawr, Pennsylvania 19010-2899 (United States)

    2014-05-21

    We report ab initio density functional theory electronic structure calculations of rotational barriers for t-butyl groups and their constituent methyl groups both in the isolated molecules and in central molecules in clusters built from the X-ray structure in four t-butyl aromatic compounds. The X-ray structures have been reported previously. We also report and interpret the temperature dependence of the solid state {sup 1}H nuclear magnetic resonance spin-lattice relaxation rate at 8.50, 22.5, and 53.0 MHz in one of the four compounds. Such experiments for the other three have been reported previously. We compare the computed barriers for methyl group and t-butyl group rotation in a central target molecule in the cluster with the activation energies determined from fitting the {sup 1}H NMR spin-lattice relaxation data. We formulate a dynamical model for the superposition of t-butyl group rotation and the rotation of the t-butyl group's constituent methyl groups. The four compounds are 2,7-di-t-butylpyrene, 1,4-di-t-butylbenzene, 2,6-di-t-butylnaphthalene, and 3-t-butylchrysene. We comment on the unusual ground state orientation of the t-butyl groups in the crystal of the pyrene and we comment on the unusually high rotational barrier of these t-butyl groups.

  5. Reaction of Ketene Dithioacetals with Pyrazolylcarbohydrazide:Synthesis and Biological Activities of Ethyl 5-Amino-1-(5'-methyl-1'-t-butyl-4'-pyrazolyl)carbonyl-3-methylthio-1H-pyrazole-4-carboxylate

    Institute of Scientific and Technical Information of China (English)

    LI Ming李明; WEN Li-Rong文丽荣; FU Wei-Jun付维军; ZHAO Gui-Long赵桂龙; HU Fang-Zhong胡方中; YANG Hua-Zheng杨华铮

    2004-01-01

    The title compound, C16-H23N5O3S, ethyl 5-amino-1-(5'-methyl-1'-t-butyl-4'-pyrazolyl)carbonyl-3-methylthio1H-pyrazole-4-carboxylate (5) has been synthesized by the treatment of ethyl 2-cyano-3,3-dimethylthioacrylate with 1-t-butyl-5-methyl-4-hydrazinocarbonylpyrazole (4) in refluxed ethanol. The possible mechanism of the above reaction was also discussed. The results of biological test show that the title compound has fungicidal and plant growth regulation activities.

  6. Synthesis and Crystal Structure of Ethyl 5-Amino-1-[(5'-methyl-1'-t-butyl-4'-pyrazolyl)carbonyl]-3- methylthio-1H-pyrazole-4-carboxylate

    Institute of Scientific and Technical Information of China (English)

    李明; 文丽荣; 赵桂龙; 王啸; 杨华铮

    2005-01-01

    The title compound, ethyl 5-amino-1-[(5'-methyl-1'-t-butyl-4'-pyrazolyl)carbonyl] -3-methylthio-1H-pyrazole-4-carboxylate 5, has been synthesized by the treatment of 4 with ethyl 2-cyano-3,3-dimethylthioacrylate, and its crystal structure was determined by X-ray diffraction method. The crystal belongs to monoclinic, space group P21/c with a = 12.194(4), b = 12.909(4), c = 11.607(4) (A), β= 90.183(5)°, V = 1827.2(10) (A)3, Mr = 365.45, Z = 4, Dc = 1.328 g/cm3, μ = 0.203 mm-1, F(000) = 776, R = 0.0586 and wR = 0.1558. Preliminary bioassays indicated that the title compound shows fungicidal and plant growth regulation activities.

  7. Synthesis and Crystal Structure of 1-(1'-t- Butyl-5'-methyl-4-pyrazolyl-carbonyl)- 3,5-dimethyl-1H-yl-pyrazole

    Institute of Scientific and Technical Information of China (English)

    文丽荣; 付维军; 李明; 赵桂龙; 胡方中; 杨华铮

    2004-01-01

    The crystal structure of 1-(1'-t-butyl-5'-methyl-4'-pyrazolylcarbonyl)-3,5-dimeth yl-1H-yl-pyrazole ([C14H20N4O]2, Mr = 520.68) has been determined by single-crystal X-ray diffraction analysis. The crystal belongs to triclinic, space group P1 with a = 11.049(4), b = 11.313(4), c = 13.964(5) A, a = 69.085(6), β = 75.962(6), γ = 62.245(6)°, V = 1436.7(9)A3, Z = 2, Dc= 1.204 g/cm3,t = 0.079 mm-1, F(000) = 560, R = 0.0790 and wR = 0.1416 for 4729 unique reflections with 2635 observed ones (I > 2σ(I)). The results indicate that the pyrazole rings display aromaticity. The four pyrazole moieties are approximately coplanar in each case. The dihedral angles between planes 1 and 2, 3 and 4 are 40.99 and 10.77°, respectively.

  8. Hydrogen bonded rings, chains and lassos: the case of t-butyl alcohol clusters

    Science.gov (United States)

    Zimmermann, D.; Häber, Th.; Schaal, H.; Suhm, M. A.

    Infrared OH stretching spectra of hydrogen bonded 2-methyl-propan-2-ol (t-butyl alcohol) clusters are investigated by ragout-jet FTIR spectroscopy. A spectral difference technique is used to discriminate approximately between neighbouring cluster sizes. Dimers, trimers and cyclic tetramers can be detected along with larger clusters, which exhibit a surprisingly structured vibrational fingerprint. Comparison is made to the spectra of related alcohols and to energetic and harmonic vibrational predictions from electronic structure calculations. The experimentally observed 32% increase in OH stretching wavenumber shift from methanol dimer to t-butyl alcohol dimer is reproduced at the HF/3-21G level (+ 33%). It is also qualitatively correct at the MP2/6-31+ G* level (+ 15%), whereas it has the wrong sign at the B3LYP/6-31+ G* level (-5%) and is negligible at the HF/6-31+ G* level, disregarding anharmonic effects. The cyclic tetramer of t-butyl alcohol is found to be particularly stable due to a favourable up-down alternation of the bulky t-butyl groups. Beyond the t-butyl alcohol tetramer, lasso structures are found to be energetically competitive with simple ring structures. A many-body decomposition shows that this is due to a reduced cooperativity in the sterically hindered pentamer ring. The resulting thermodynamic and kinetic relevance of cyclic tetramers is discussed.

  9. Research Progress in Microbiological Degradation of Bensulfuron-Methyl Herbicide

    Institute of Scientific and Technical Information of China (English)

    XIONG Minghua; LI Chunyan

    2009-01-01

    This paper reviewed the strategies and methods of screening for microorganisms having strong ability to remove bensulfuron-methyl (BSM), and discussed BSM degradation pathways and factors affecting its microbial metabolism. Finally, it prospected the research emphasis in the future.

  10. Molecular recognition study of ethosuximide by the supramolecular probe, p-t-butyl calix(8)arene

    Energy Technology Data Exchange (ETDEWEB)

    Meenakshi, C., E-mail: geethu.laxi@gmail.com [Department of Chemistry, Shri Meenakshi Government College for Women (Autonomous), Madurai 625002 (India); Sangeetha, P.; Ramakrishnan, V. [Department of Laser Studies, School of Physics, Madurai Kamaraj University, Madurai 625021 (India)

    2013-06-15

    The supramolecule, p-t-Butyl calix(8)arene, forms inclusion complex with the antiseizure drug molecule, ethosuximide. This feature is explained on the basis of optical absorption spectroscopy. Here p-t-Butyl calix(8)arene is the host molecule and ethosuximide is the guest molecule. The stoichiometry of the host–guest complex and the binding constant has been determined using Benesi–Hildebrand plot. Based on the result obtained the structure of the inclusion complex has been proposed. -- Highlights: ► Third generation supramolecule, t-butyl calix (8) arene, is used as a host molecule. ► Anti seizure drug molecule is used as a guest molecule. ► Inclusion complex is formed between the host and guest molecule.

  11. Stabilizing effects of estertins mercaptide (methyl acrylate) for PVC degradation

    Science.gov (United States)

    Zhang, S. H.; Liu, T. M.; Li, J. L.; Wang, C. R.; Li, C.; Wang, Z. Q.

    2016-07-01

    The thermal and UV light (ultraviolet light) stability of PVC films with estertins mercaptide (methyl acrylate), methyltins mercaptide and the compound consisted of estertins mercaptide (methyl acrylate) and hydrotalcite (2:2.5) were investigated by ageing in a circulation oven at 190 °C and irradiating with 72W UV light for 96h, respectively, and then the yellowness and transmission rate were tested by Color Quest XE. Hydrotalcite was proved to have good synergies with estertins mercaptide (methyl acrylate) on improving the thermal stability and UV light stability. The retarding effects of the heat stabilizers to PVC degradation were tested by TGA from 50°C to 600°C. The results show that temperature of HCl evolution from PVC film was improved obviously by compounding with estertins mercaptide(methyl acrylate) and hydrotalcite and estertins mercaptide(methyl acrylate) was found to have a better long term stability. Sn4+ consistence of water and seawater in which films before and after UV light irradiation were soaked for 60 days was analyzed by ICP; the results indicate that the Sn4+ consistence from the films with estertins mercaptide(methyl acrylate) as thermal stabilizer was lower than that from the film with methyltins mercaptide. The crosslink moderately by UV irradiation for PVC films can hold back the dissolution of organotin heat stabilizers from PVC products into water and seawater.

  12. Tri(t-butyl)phosphine-assisted selective hydrosilylation of terminal alkynes

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    A highly efficient and regio-/stereoselective method of hydrosilylating terminal alkynes was developed using Pt(DVDS)-tri(t-butyl) phosphine catalyst system at room temperature.Trans-products or alpha-products were obtained almost exclusively depending on the alkynes and silanes employed.

  13. Degradation of methyl orange through synergistic effect of zirconia nanotubes and ultrasonic wave.

    Science.gov (United States)

    Zhao, Jianling; Wang, Xixin; Zhang, Libin; Hou, Xiaorui; Li, Ying; Tang, Chengchun

    2011-04-15

    Zirconia nanotubes with a length of 25 μm, inner diameter of 80 nm, and wall thickness of 35 nm were prepared by anodization method in mixture of formamide and glycerol (volume ratio = 1:1) containing 1 wt% NH(4)F and 1 wt% H(2)O. Experiments showed that zirconia nanotubes and ultrasonic wave had synergistic degradation effect for methyl orange and the efficiency of ultrasonic wave increased by more than 7 times. The decolorization percentage was influenced by pH value of the solution. Methyl orange was easy to be degraded in acidic solution. The decolorization percentage of methyl orange reached 97.6% when degraded for 8h in 20mg/L methyl orange solution with optimal pH value 2. The reason of synergistic degradation effect for methyl orange might be that adsorption of methyl orange onto zirconia nanotubes resulted in the easy degradation of the methyl orange through ultrasonic wave.

  14. Rapid degradation of bensulfuron-methyl upon repeated application in paddy soils

    Institute of Scientific and Technical Information of China (English)

    XIE Xiao-mei; LIU Wei-ping; ABID Subhani

    2004-01-01

    Rapid degradation of bensulfuron-methyl upon repeated application in paddy soils was studied. The results showed that the DT50of bensulfuron-methyl was reduced from 16 d to 9 d in soil with one-year bensulfuron-methyl application. Rapid bensulfuron-methyl degradation was happened to previously untreated soil by addition 5% rapid bensuifuron-methyl adapted soil and was inhibited following pre-treatment with broad-spectrum antibiotic chloramphenicol. In bensulfuron-methyl adapted soil mineralisation of 14C labeled bensulfuronmethyl to 14 CO2 occurred at a faster rate than with previously untreated soil. It was concluded that rapid bensulfuron-methyl degradation upon repeated application is probably linked to the adaptation of soil bacteria which can utilize bensulfuron-methyl as a source of carbon and energy.

  15. Thermal degradation behavior of methyl methacrylate derived copolymer.

    Science.gov (United States)

    Kaya, Esin; Kurt, Adnan; Er, Mustafa

    2012-11-01

    A novel copolymer of 2-hydroxy-3-menthyloxy-1-(4-methoxyphenyl)-3-oxopropyl methacrylate (HMOPMA) and methyl methacrylate (MMA), [poly(HMOPMA-co-MMA)], was synthesized by free radical polymerization. The percentages of HMOPMA and MMA units obtained in the copolymer composition were 19% and 81%, respectively. The solubility parameter of poly(HMOPMA-co-MMA) was found to be 10.3 cal(1/2) cm(-3/2) by turbidimetric titration method. Thermal degradation mechanism and activation energies for initial decomposition process under non-isothermal conditions were determined by integral approximation methods from the thermogravimetric study. The decomposition activation energies of poly(HMOPMA-co-MMA) using Kissinger and Flyn-Wall-Ozawa methods were calculated as 119.99 kJ/mol and 125.34 kJ/mol, respectively. The study of kinetic equations showed that the reaction mechanism of decomposition process in the conversion range studied progressed with D1 mechanism, one-dimensional diffusion of deceleration type of solid state mechanism.

  16. Ethyl t-butyl ether: review of reproductive and developmental toxicity.

    Science.gov (United States)

    de Peyster, Ann

    2010-06-01

    Ethyl t-butyl ether (ETBE) is a motor fuel oxygenate used in reformulated gasoline. Knowledge of developmental and reproductive toxicity potential of ETBE is critical for making informed decisions about acceptance and regulations. This review discusses toxicology studies providing information about effects on reproduction and the conceptus. Seven GLP-compliant studies following widely accepted protocols have focused specifically on developmental and reproductive toxicity (DART) in rats and rabbits exposed to ETBE by gavage with doses up to 1,000 mg/kg body weight/day, the limit specified in standardized test guidelines. Other repeat-dose general toxicology studies have administered ETBE to rodents for up to 180 days, and included reproductive organ weights, histology, or other indications of reproductive system structure or function. DART potential of the main ETBE metabolite t-butyl alcohol and class-related MTBE has also been studied. More GLP-compliant studies exist for evaluating ETBE using well-established, currently recommended protocols than are available for many other chemicals used today. The database for determining ETBE DART potential is adequate, although not all study details are currently easily accessible for peer-review. ETBE does not appear to be selectively toxic to reproduction or embryofetal development in the absence of other manifestations of general toxicity. Studies using recommended methods for sample preservation and analysis have shown no targeted effect on the reproductive system. No embryofetal effects were observed in rabbits. Early postnatal rat pup deaths show no clear dose-response and have largely been attributed to total litter losses with accompanying evidence of maternal neglect or frank maternal morbidity.

  17. Effect of anionic surfactants on the process of Fenton degradation of methyl orange.

    Science.gov (United States)

    Yang, C W; Wang, D

    2009-01-01

    Fenton process has been shown to be very successful to remove dyes from water. However, the influence of other constituents in dyeing industry wastewater, such as Sodium Dodecyl Sulphate (SDS) surfactants, has not been investigated. In this study, the effect of SDS surfactant on the kinetics of Methyl Orange degradation undergoing Fenton process was investigated. Results show that Methyl Orange degradation rate decreased as SDS concentration increased, which was attributed to the consumption of hydroxyl radicals (OH) by surfactants and the formation of Methyl Orange-SDS complex. No evidence was found that the Methyl Orange degradation pathway was affected by the presence of SDS. The kinetics modelling indicates the reaction was the first-order reaction to Methyl Orange.

  18. Influence of crystal structure of nanosized ZrO2 on photocatalytic degradation of methyl orange

    OpenAIRE

    Basahel, Sulaiman N; Ali, Tarek T; Mokhtar, Mohamed; Narasimharao, Katabathini

    2015-01-01

    Nanosized ZrO2 powders with near pure monoclinic, tetragonal, and cubic structures synthesized by various methods were used as catalysts for photocatalytic degradation of methyl orange. The structural and textural properties of the samples were analyzed by X-ray diffraction, Raman spectroscopy, TEM, UV-vis, X-ray photoelectron spectroscopy (XPS), and N2 adsorption measurements. The performance of synthesized ZrO2 nanoparticles in the photocatalytic degradation of methyl orange under UV light ...

  19. Magnetic field assisted Fenton reactions for the enhanced degradation of methyl blue

    Institute of Scientific and Technical Information of China (English)

    Xiao Long Hao; Lu Yi Zou; Guang Sheng Zhang; Yi Bo Zhang

    2009-01-01

    Magnetic field was tentatively introduced into Fenton reactions system for the degradation and discoloration of methyl blue as the represent of organic chemical dye, which was a bio-refractory organic pollutant in industry wastewater. It was found that under optimal Fenton reaction conditions, with the assistant of magnetic field in Fenton reactions, the degradation rate of methyl blue, the decomposition rate of H2O2 and the conversion rate of Fe2+ were accelerated, the extent of them would be improved by the increase of magnetic field intensity. Meanwhile, the mineralization of methyl blue (CODcr) was improved by over 10% with magnetic fiold.

  20. MnO2/CeO2 for catalytic ultrasonic degradation of methyl orange.

    Science.gov (United States)

    Zhao, He; Zhang, Guangming; Zhang, Quanling

    2014-05-01

    Catalytic ultrasonic degradation of aqueous methyl orange was studied in this paper. Heterogeneous catalyst MnO2/CeO2 was prepared by impregnation of manganese oxide on cerium oxide. Morphology and specific surface area of MnO2/CeO2 catalyst were characterized and its composition was determined. Results showed big differences between fresh and used catalyst. The removal efficiency of methyl orange by MnO2/CeO2 catalytic ultrasonic process was investigated. Results showed that ultrasonic process could remove 3.5% of methyl orange while catalytic ultrasonic process could remove 85% of methyl orange in 10 min. The effects of free radical scavengers were studied to determine the role of hydroxyl free radical in catalytic ultrasonic process. Results showed that methyl orange degradation efficiency declined after adding free radical scavengers, illustrating that hydroxyl free radical played an important role in degrading methyl orange. Theoretic analysis showed that the resonance size of cavitation bubbles was comparable with the size of catalyst particles. Thus, catalyst particles might act as cavitation nucleus and enhance ultrasonic cavitation effects. Measurement of H2O2 concentration in catalytic ultrasonic process confirmed this hypothesis. Effects of pre-adsorption on catalytic ultrasonic process were examined. Pre-adsorption significantly improved methyl orange removal. The potential explanation was that methyl orange molecules adsorbed on catalysts could enter cavitation bubbles and undergo stronger cavitation.

  1. Degradation of organophosphorus pesticide parathion methyl on nanostructured titania-iron mixed oxides

    Energy Technology Data Exchange (ETDEWEB)

    Henych, Jiří, E-mail: henych@iic.cas.cz [Department of Material Chemistry, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Řež (Czech Republic); Štengl, Václav; Slušná, Michaela; Matys Grygar, Tomáš [Department of Material Chemistry, Institute of Inorganic Chemistry AS CR v.v.i., 25068 Řež (Czech Republic); Janoš, Pavel; Kuráň, Pavel; Štastný, Martin [Faculty of the Environment, J.E. Purkyně University, Králova Výšina 7, 400 96 Ústí nad Labem (Czech Republic)

    2015-07-30

    Highlights: • Ti–Fe mixed oxides were synthesized via low-temperature one-pot method. • Mixed oxides were used for degradation of parathion methyl. • Pure reference oxide samples showed no degradation ability. • Mixed oxides reached 70% degree of conversion of parathion methyl. - Abstract: Titania-iron mixed oxides with various Ti:Fe ratio were prepared by homogeneous hydrolysis of aqueous solutions of titanium(IV) oxysulphate and iron(III) sulphate with urea as a precipitating agent. The synthesized samples were characterized by X-ray diffraction, Raman and infrared spectroscopy, scanning and transmission electron microscopy, XRF analysis, specific surface area (BET) and porosity determination (BJH). These oxides were used for degradation of organophosporus pesticide parathion methyl. The highest degradation efficiency approaching <70% was found for the samples with Ti:Fe ratio 0.25:1 and 1:0.25. Contrary, parathion methyl was not degraded on the surfaces of pure oxides. In general, the highest degradation rate exhibited samples consisted of the iron or titanium oxide containing a moderate amount of the admixture. However, distinct correlations between the degradation rate and the sorbent composition were not identified.

  2. Rapid degradation of azo dye methyl orange using hollow cobalt nanoparticles.

    Science.gov (United States)

    Sha, Yingying; Mathew, Iswarya; Cui, Qingzhou; Clay, Molly; Gao, Fan; Zhang, Xiaoqi Jackie; Gu, Zhiyong

    2016-02-01

    A rapid and efficient method for methyl orange degradation using hollow cobalt (Co) nanoparticles is reported. Hollow Co nanoparticles were fabricated by a galvanic replacement reaction using aluminum (Al) nanoparticles as the template material. The methyl orange degradation characteristics were investigated by measuring the time dependent UV-Vis absorption of the dye solution, which showed a very fast degradation rate under acidic conditions. At an initial methyl orange concentration of 100 mg/L (pH = 2.5) and Co nanoparticle dosage of 0.5 g/L, the azo dye degradation efficiency reached up to 99% within 4 min, and the degradation constant rate was up to 2.444 min(-1), which is the highest value among other studies. A comparison of the decolorization rates at similar conditions with several other azo dyes, including Congo red, Amaranth, and Orange G, showed that the dye with a simpler structure and lower molecular mass decolorized considerably faster than the ones having a more complicated structure (higher molecular mass). The methyl orange degradation was also conducted using hollow nickel (Ni) nanoparticles and commercially available solid spherical Co and Ni nanoparticles. The results showed that Co-based nanoparticles outperformed Ni-based nanoparticles, with the hollow Co nanoparticles exhibiting the fastest degradation rate. Using the hollow Co nanoparticles is a very promising approach for the remediation of methyl orange dye containing wastewater due to the fast degradation rate and high degradation efficiency. In addition, these hollow Co nanoparticles are easily recycled because of their magnetic property.

  3. Construction and analysis of an intergeneric fusant able to degrade bensulfuron-methyl and butachlor.

    Science.gov (United States)

    Feng, Liping; Xiong, Minghua; Cheng, Xiaosong; Hou, Ning; Li, Chunyan

    2013-02-01

    Rhodococcus sp. BX2 degrades bensulfuron-methyl but not butachlor, and Acinetobacter sp. LYC-1 degrades butachlor but not bensulfuron-methyl. Functional strains were constructed through protoplast fusion of Rhodococcus sp. BX2 and Acinetobacter sp. LYC-1 to generate fusants with an improved ability to simultaneously degrade bensulfuron-methyl and butachlor. Initial identification and stability tests of the fusants were performed. Three fusants with eighth transfer on plates containing two antibiotics and two herbicides were obtained. F1 also grew well in an inorganic salt solution containing bensulfuron-methyl and butachlor. F1 was characterized by its parents' morphological and physio-biochemical features. F1 not only had bands in common with BX2 and LYC-1, but also had its own specific bands analyzed by Random Amplified Polymorphic DNA. The genetic similarity indices between F1 and BX2 and F1 and LYC-1 were 0.507 and 0.470, respectively. The percentages bensulfuron-methyl and butachlor degradation by F1 in an inorganic salt solution supplemented with 100 mg/L bensulfuron-methyl and 100 mg/L butachlor were 65.35 and 62.41 %, respectively, and the percentages in soil contaminated with 10 mg/kg bensulfuron-methyl and 10 mg/kg butachlor with an inoculum size of 5 % at 34 °C and at a pH of 7.5 after 35 days were 63.74 and 61.53 %, respectively. It was demonstrated that F1 could simultaneously degrade bensulfuron-methyl and butachlor.

  4. The adsorption and degradation of chlorpyriphos-methyl, pendimethalin and metalaxyl in solid urban waste compost.

    Science.gov (United States)

    Baglieri, Andrea; Gennari, Mara; Arena, Maria; Abbate, Cristina

    2011-01-01

    To evaluate the feasibility of using compost to prepare substrates for the disposal of pesticide residues, adsorption and degradation studies were carried out on three widely used agricultural pesticides: chlorpyriphos-methyl, pendimethalin and metalaxyl. Obtained from solid urban waste, this compost has been shown to be able to adsorb high levels of chlorpyriphos-methyl and pendimethalin (85%, 100%) whereas metalaxyl was only adsorbed at a level of 37%. However, adding smectite to the compost increased the adsorption of metalaxyl by 117%. Chlorpyriphos-methyl and pendimethalin degraded quickly with half-lives of 1.7 and 14.5 days, respectively, whereas metalaxyl proved more persistent (a half-life of 84 days). Adding ammonium nitrate to the compost accelerated metalaxyl degradation to a half-life of 15 days.

  5. Preparation of Mixed Semiconductors for Methyl Orange Degradation

    OpenAIRE

    Sangeeta Adhikari; Debasish Sarkar

    2015-01-01

    Attempts were made to compare the photocatalytic efficacy in between quasi-fiber and near spherical commercial grade ZnO through the addition of monoclinic WO3 nanocuboid. Mixed oxide semiconductors were assessed for their dye degradation performance under irradiation of visible light energy. Surface area and the particle morphology pattern have an influence on the resultant photocatalytic features of these mixed oxide composites. The high porous quasi-fibrous ZnO was successfully fabricated ...

  6. Estimation of the fraction of biologically active methyl tert-butyl ether degraders in a heterogeneous biomass sample

    DEFF Research Database (Denmark)

    Waul, Christopher Kevin; Arvin, Erik; Schmidt, Jens Ejbye

    2008-01-01

    The fraction of biologically active methyl tert-butyl ether degraders in reactors is just as important for prediction of removal rates as knowledge of the kinetic parameters. The fraction of biologically active methyl tert-butyl ether degraders in a heterogeneous biomass sample, taken from a packed...

  7. Isolation and Characterization of Methyl Parathion-degrading Bacteria Based on Microbial Sensor Construction

    Directory of Open Access Journals (Sweden)

    GENG Fang-fang

    2014-12-01

    Full Text Available Methyl parathion (MP, a kind of typical organophosphates pesticides (OPs, is widely used as agricultural insecticides. However, due to their neurotoxic effects on humans, the elimination of OPs has become increasingly important. Microbial sensors are consisted of biological components and transducers. Owing to their attractive advantages including low cost, easy of miniaturization and excellent selectivity, they have been widely used for environmental analysis. In this paper, four novel bacterial strains capable of utilizing methyl parathion as the sole carbon source were isolated from pesticide contaminated soils. These four isolates were identified based on morphological characteristics and 16S rRNA gene sequences analysis, and their capability of degrading methyl parathion were investigated by high performance liquid chromatography. The highest degrading efficiency strain was selected for further study of degrading mechanism. The results indicated that degradation rate of these four strains were all over 78% after incubation at 30 ℃, pH 7.0 for 7 d with the original concentration of methyl parathion 50 mg·L-1. The highest degradation rate was up to 100%. 16S rRNA gene sequences indicated that strain MP-6 was affiliated into the genus klebsiella. The LC-MS results indicated that methyl parathion was hydrolyzed to dimethyl thiophosphoric acid and p-nitrophenol by MP-6. A little of p-nitrophenol molecules could be further metabolized to 4-nitrocatechol and 1, 2, 4-benzenetrio. The results indicated that based on detecting the potential signal of intermediate product p-nitrophenol, the strain MP-6 could be used to construct microbial sensors for determination of organophosphorus pesticides in environment.

  8. Net degradation of methyl mercury in alder swamps.

    Science.gov (United States)

    Kronberg, Rose-Marie; Tjerngren, Ida; Drott, Andreas; Björn, Erik; Skyllberg, Ulf

    2012-12-18

    Wetlands are generally considered to be sources of methyl mercury (MeHg) in northern temperate landscapes. However, a recent input-output mass balance study during 2007-2010 revealed a black alder (Alnus glutinosa) swamp in southern Sweden to be a consistent and significant MeHg sink, with a 30-60% loss of MeHg. The soil pool of MeHg varied substantially between years, but it always decreased with distance from the stream inlet to the swamp. The soil MeHg pool was significantly lower in the downstream as compared to the upstream half of the swamp (0.66 and 1.34 ng MeHg g⁻¹ SOC⁻¹ annual average⁻¹, respectively, one-way ANOVA, p = 0.0006). In 2008 a significant decrease of %MeHg in soil was paralleled by a significant increase in potential demethylation rate constant (k(d), p landscape planning, and suggest that restored or preserved Alnus swamps may be used to mitigate MeHg produced in northern temperate landscapes.

  9. Rheology and thermal degradation of isocyanate-functionalized methyl cellulose-based oleogels.

    Science.gov (United States)

    Gallego, R; Arteaga, J F; Valencia, C; Franco, J M

    2013-10-15

    The -NCO-functionalization of methyl cellulose with HMDI and its application to chemically gel the castor oil is explored in this work by analyzing the influence of functionalization degree on the rheological and thermogravimetric behavior of resulting chemical oleogels. With this aim, different methyl cellulose chemical modifications were achieved by limiting the proportion of HMDI and, subsequently, oleogels were obtained by dispersing these polymers in castor oil and promoting the reaction between those biopolymers and the hydroxyl groups located in the ricinoleic fatty acid chain. -NCO-functionalized methyl cellulose-based oleogels were characterized from themogravimetric and rheological points of view. Suitable thermal resistance and rheological characteristics were found in order to propose these oleogels as promising bio-based alternatives to traditional lubricating greases based on non-renewable resources. In general, -NCO-functionalized methyl cellulose thermally decomposed in three main steps whereas resulting oleogels thermal decomposition takes place in one main single stage which comprises the thermal degradation of both the polymer and the castor oil. Temperature range for thermal degradation is broadened when using highly -NCO-functionalized methyl cellulose. A cross-linked viscoelastic gel was obtained with methyl cellulose functionalized in a relatively low degree (around 6% -NCO molar content). The rheological properties of highly functionalized methyl cellulose-based oleogels evolve during several months of aging, but mainly during the first week, due to the progress of the reaction between -NCO functional groups and castor oil -OH groups. SAOS functions analyzed and oleogel relative elasticity increase with the functionalization degree. Oleogel linear viscoelastic response is also extremely dependent on NCO-functionalized methyl cellulose concentration.

  10. Degradation of organophosphorus pesticide parathion methyl on nanostructured titania-iron mixed oxides

    Science.gov (United States)

    Henych, Jiří; Štengl, Václav; Slušná, Michaela; Matys Grygar, Tomáš; Janoš, Pavel; Kuráň, Pavel; Štastný, Martin

    2015-07-01

    Titania-iron mixed oxides with various Ti:Fe ratio were prepared by homogeneous hydrolysis of aqueous solutions of titanium(IV) oxysulphate and iron(III) sulphate with urea as a precipitating agent. The synthesized samples were characterized by X-ray diffraction, Raman and infrared spectroscopy, scanning and transmission electron microscopy, XRF analysis, specific surface area (BET) and porosity determination (BJH). These oxides were used for degradation of organophosporus pesticide parathion methyl. The highest degradation efficiency approaching degraded on the surfaces of pure oxides. In general, the highest degradation rate exhibited samples consisted of the iron or titanium oxide containing a moderate amount of the admixture. However, distinct correlations between the degradation rate and the sorbent composition were not identified.

  11. A novel two-level dielectric barrier discharge reactor for methyl orange degradation.

    Science.gov (United States)

    Tao, Xumei; Wang, Guowei; Huang, Liang; Ye, Qingguo; Xu, Dongyan

    2016-12-15

    A novel pilot two-level dielectric barrier discharge (DBD) reactor has been proposed and applied for degradation of continuous model wastewater. The two-level DBD reactor was skillfully realized with high space utilization efficiency and large contact area between plasma and wastewater. Various conditions such as applied voltage, initial concentration and initial pH value on methyl orange (MO) model wastewater degradation were investigated. The results showed that the appropriate applied voltage was 13.4 kV; low initial concentration and low initial pH value were conducive for MO degradation. The percentage removal of 4 L MO with concentration of 80 mg/L reached 94.1% after plasma treatment for 80min. Based on ultraviolet spectrum (UV), Infrared spectrum (IR), liquid chromatography-mass spectrometry (LC-MS) analysis of degradation intermediates and products, insights in the degradation pathway of MO were proposed.

  12. Photocatalytic degradation of methyl orange using ZnO/TiO2 composites

    Institute of Scientific and Technical Information of China (English)

    Ming GE; Changsheng GUO; Xingwang ZHU; Lili MA; Zhefian HAN; Wei HU; Yuqiu WANG

    2009-01-01

    ZnO/TiO2 composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange (MO) in aqueous suspension under UV irradiation. The composi-tion and surface structure of the catalyst were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscopy (TEM). The degradation efficiencies of MO at various pH values were obtained. The highest degradation efficiencies were obtained before 30 min and after 60 min at pH 11.0 and pH 2.0, respectively. A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry. Six intermediates were found during the photocatalytic degradation process of quinonoid MO. The degradation pathway of quinonoid MO was also proposed.

  13. Preparation of Mixed Semiconductors for Methyl Orange Degradation

    Directory of Open Access Journals (Sweden)

    Sangeeta Adhikari

    2015-01-01

    Full Text Available Attempts were made to compare the photocatalytic efficacy in between quasi-fiber and near spherical commercial grade ZnO through the addition of monoclinic WO3 nanocuboid. Mixed oxide semiconductors were assessed for their dye degradation performance under irradiation of visible light energy. Surface area and the particle morphology pattern have an influence on the resultant photocatalytic features of these mixed oxide composites. The high porous quasi-fibrous ZnO was successfully fabricated by a simple solution combustion method. It is deliberately made of clusters of primary near spherical particles that supports WO3 nanocuboid embedment and shows interactive characteristics in comparison to the counterpart commercial near spherical ZnO combined with WO3. The photocatalytic activity significantly increases up to 95% under visible radiation for 90 min due to high surface area imparted by unique quasi-fiber morphology. The photogenerated electron-hole pair interaction mechanism has been proposed to support the photocatalytic behavior.

  14. Activity of cell wall degrading glycanases in methyl jasmonate-induced leaf abscission in Kalanchoe blossfeldiana

    Directory of Open Access Journals (Sweden)

    Marian Saniewski

    2013-12-01

    Full Text Available It was found previously that methyl jasmonate (JA-Me induced leaf abscission in Kalanchoe blossfeldiana. In present studies it was shown that JA-Me markedly increased the total activities of cellulase, polygalacturonase, pectinase and xylanase in petioles, but did not affect activities of these enzymes in the blades and apical part of shoots of K. blossfeldiana. These results suggest that methyl jasmonate promotes the degradation of cell wall polysaccharides in the abscission zone and in this way induces leaf abscission in Kalanchoe blossfeldiana.

  15. Ultrasonic Degradation of Methyl Orange in Presence of Y2O3 Doping Anatase TiO2 Catalyst

    Institute of Scientific and Technical Information of China (English)

    Wang Jun; Guo Baodong; Pan Zhijun; Liu Zhenrong; Wen Fuyu; Zhang Zhaohong

    2004-01-01

    Various affecting factors and degradation mechanism were studied on ultrasonic degradation of methyl orange adopting Y2O3 doping anatase TiO2 catalyst prepared in laboratory.In the experiment, the UV-VIS spectrophotometer was used to follow and inspect the degradation process of methyl orange.The results indicate that the ultrasonic degradation ratios of methyl orange in the presence of anatase TiO2 catalyst are much better than those without catalyst.Moreover, the catalytic performance of Y2O3 doping anatase TiO2 catalyst is obviously higher than that of anatase TiO2 catalyst without doping.The optimal conditions were adopted in this work and the degradation and COD elimination ratio of methyl orange got to98% and 99.0% in 90 min, respectively.

  16. Degradation of Methyl Orange in Water by Contact Glow Discharge Electrolysis

    Institute of Scientific and Technical Information of China (English)

    GONG Jianying; CAI Weimin

    2007-01-01

    The degradation of methyl orange in a neutral phosphate buffer solution was investigated by means of contact glow discharge electrolysis (CGDE).The methyl oranges were degraded and eventually decomposed into inorganic carbon when CGDE was conducted under the applied DC voltage of 480 V and current of ca.80 mA.As the intermediate products,some phenolic compounds were detected as well as carboxylic acids.Experimental results showed that the oxidation process followed the first-order reaction law.Based on the analysis of the ultraviolet (UV) spectra of the solution and the intermediate products from High Pressure Liquid Chromatography-Mass Spectrum (HPLC-MS),the reaction pathway was proposed.The attack of hydroxyl radicals was considered to be a key step to start the whole oxidation process.

  17. Influence of crystal structure of nanosized ZrO2 on photocatalytic degradation of methyl orange

    Science.gov (United States)

    Basahel, Sulaiman N.; Ali, Tarek T.; Mokhtar, Mohamed; Narasimharao, Katabathini

    2015-02-01

    Nanosized ZrO2 powders with near pure monoclinic, tetragonal, and cubic structures synthesized by various methods were used as catalysts for photocatalytic degradation of methyl orange. The structural and textural properties of the samples were analyzed by X-ray diffraction, Raman spectroscopy, TEM, UV-vis, X-ray photoelectron spectroscopy (XPS), and N2 adsorption measurements. The performance of synthesized ZrO2 nanoparticles in the photocatalytic degradation of methyl orange under UV light irradiation was evaluated. The photocatalytic activity of the pure monoclinic ZrO2 sample is higher than that of the tetragonal and cubic ZrO2 samples under optimum identical conditions. The characterization results revealed that monoclinic ZrO2 nanoparticles possessed high crystallinity and mesopores with diameter of 100 Å. The higher activity of the monoclinic ZrO2 sample for the photocatalytic degradation of methyl orange can be attributed to the combining effects of factors including the presence of small amount of oxygen-deficient zirconium oxide phase, high crystallinity, large pores, and high density of surface hydroxyl groups.

  18. Photocatalytic degradation of methyl orange by polyoxometalates supported on yttrium-doped TiO2

    Institute of Scientific and Technical Information of China (English)

    WANG Yajun; LU Kecheng; FENG Changgen

    2011-01-01

    A series of novel photocatalysts,H3PW12O40-Y-TiO2 nanocomposites with different H3PW12O40 loading levels (10%-40%) were prepared by impregnation method.And the Y-TiO2 support,doped with yttrium,was synthesized via sol-gel technique.The prepared catalysts were characterized by Fourier transform infrared spectroscopy (FT-IR),powder X-ray diffraction (XRD),nitrogen adsorption-desorption analysis and scanning electron microscopy (SEM).The processes allowed obtaining Keggin structure and crystallized anatase with large BET surface area as well as uniform distribution.The effects of H3PW12O40 loadings,catalyst dose,initial pH and concentration of dye solution on the degradation kinetics of methyl orange under UV light (λ≥365 nm) were discussed.Kinetics studies showed that the photocatalytic degradation of methyl orange fitted the apparent first-order reaction.Methyl orange was totally degraded in 21 min under optimum conditions:20% loading,0.03 g dose and pH 1.0.The catalyst was stable and easily to be separated from reaction system for recovery.

  19. Photocatalytic degradation of methyl orange dye using silver (Ag) nanoparticles synthesized from Ulva lactuca.

    Science.gov (United States)

    Kumar, P; Govindaraju, M; Senthamilselvi, S; Premkumar, K

    2013-03-01

    In this paper, we report on biosynthesis of silver nanoparticles using Ulva lactuca (seaweed) at room temperature along with photocatalytic degradation of methyl orange dye. UV spectral analysis showed peak at 430 nm with special reference to the excitation of surfaces plasmon vibration by silver nanoparticles. FT-IR studies reveal the presence of bioactive functional groups such as phenolic compounds, amines and aromatic ring are found to be the capping and stabilizing agents of nanoparticles. The morphology of silver nanoparticles was found to be spherical and ranges about 48.59 nm as confirmed by HR-SEM. Negative zeta potential value of -34 mV suggests that the nanoparticles are highly stable in colloidal solution. XRD patterns also suggest the occurrence of spherical shaped particles due to the presence of silver ions. Further, photocatalytic degradation of methyl orange was measured spectrophotometrically by using silver as nanocatalyst under visible light illumination. The results revealed that biosynthesized silver nanoparticles using U. lactuca was found to be impressive in degrading methyl orange.

  20. Influence of crystal structure of nanosized ZrO2 on photocatalytic degradation of methyl orange.

    Science.gov (United States)

    Basahel, Sulaiman N; Ali, Tarek T; Mokhtar, Mohamed; Narasimharao, Katabathini

    2015-01-01

    Nanosized ZrO2 powders with near pure monoclinic, tetragonal, and cubic structures synthesized by various methods were used as catalysts for photocatalytic degradation of methyl orange. The structural and textural properties of the samples were analyzed by X-ray diffraction, Raman spectroscopy, TEM, UV-vis, X-ray photoelectron spectroscopy (XPS), and N2 adsorption measurements. The performance of synthesized ZrO2 nanoparticles in the photocatalytic degradation of methyl orange under UV light irradiation was evaluated. The photocatalytic activity of the pure monoclinic ZrO2 sample is higher than that of the tetragonal and cubic ZrO2 samples under optimum identical conditions. The characterization results revealed that monoclinic ZrO2 nanoparticles possessed high crystallinity and mesopores with diameter of 100 Å. The higher activity of the monoclinic ZrO2 sample for the photocatalytic degradation of methyl orange can be attributed to the combining effects of factors including the presence of small amount of oxygen-deficient zirconium oxide phase, high crystallinity, large pores, and high density of surface hydroxyl groups.

  1. Hydrogen bonding in the recovery of phenols and methyl-t-butyl ether : molecular modeling and calorimetry

    NARCIS (Netherlands)

    Cuypers, R.

    2010-01-01

    The purification of waste water is very important, for clean potable water is a common good and a necessity. Surface water purification is nowadays carried out on a massive industrial scale, and clean water is at our disposal virtually everywhere and always. However, cleaning industrial waste water

  2. Enhanced degradation of the volatile fumigant-nematicides 1,3-d and methyl bromide in soil.

    Science.gov (United States)

    Ou, L T

    1998-03-01

    The use of the gaseous funaigant-nematicide methyl bromide in agriculture is scheduled to be phased out in the year 2001.1,3-Dichloropropene (1,3-D) in combination with chloropicrin and an herbicide is considered to be a viable alternative to methyl bromide for some crops. 1,3-Dichloropropene consists of two isomers, cis- and trans-l,3-D. A number of soil bacteria have been shown to initially degrade 1,3-D or one of its isomers, cis-l,3-D, via hydrolysis. Until recently, the degradation of cis- and trans-l,3-D in soils was considered to exhibit similar kinetics, witla their degradation rates increasing with increases in soil temperature. Enhanced degradation of 1,3-D in soil from a site in Florida with a history of repeated annual applications of 1,3-D was observed in 1994. Biological hydrolysis was involved in the initial degradation of cis- and trans-l,3-D. The two isomers were degraded at different rates, with the trans isomer being degraded more rapidly than the cis isomer. Cis- and trans-l,3-D in soil from the control site were degraded at a similar rate but more slowly than in the enhanced soil. Methyl bromide in soils can be degraded through chemical hydrolysis and methylation to soil organic matter. Some methanotrophic bacteria and ammonia-oxidation bacteria during the oxidation of their primary substrates (methane and ammonia) also have the capacity to cooxidize methyl bromide to formaldehyde and bromide ion. It was recently observed that degradation of methyl bromide was stimulated in methanotrophic soils and in soils treated with ammonium sulfate. Soil methanotrophic bacteria and soil nitrifiers are apparently responsible for cooxidation of methyl bromide in methanotrophic and ammonia treated soils, respectively.

  3. Complete Genome of Rhodococcus pyridinivorans SB3094, a Methyl-Ethyl-Ketone-Degrading Bacterium Used for Bioaugmentation

    DEFF Research Database (Denmark)

    Dueholm, Morten Simonsen; Albertsen, Mads; D'Imperio, Seth;

    2014-01-01

    Here, we present the complete genome of Rhodococcus pyridinivorans SB3094, a methyl-ethyl-ketone (MEK)-degrading strain used for bioaugmentation relating to the treatment of wastewater contamination with petrochemical hydrocarbons. The genome highlights important features for bioaugmentation...

  4. Microbial degradation of methyl tert-butyl ether and tert-butyl alcohol in the subsurface

    Science.gov (United States)

    Schmidt, Torsten C.; Schirmer, Mario; Weiß, Holger; Haderlein, Stefan B.

    2004-06-01

    The fate of fuel oxygenates such as methyl tert-butyl ether (MTBE) in the subsurface is governed by their degradability under various redox conditions. The key intermediate in degradation of MTBE and ethyl tert-butyl ether (ETBE) is tert-butyl alcohol (TBA) which was often found as accumulating intermediate or dead-end product in lab studies using microcosms or isolated cell suspensions. This review discusses in detail the thermodynamics of the degradation processes utilizing various terminal electron acceptors, and the aerobic degradation pathways of MTBE and TBA. It summarizes the present knowledge on MTBE and TBA degradation gained from either microcosm or pure culture studies and emphasizes the potential of compound-specific isotope analysis (CSIA) for identification and quantification of degradation processes of slowly biodegradable pollutants such as MTBE and TBA. Microcosm studies demonstrated that MTBE and TBA may be biodegradable under oxic and nearly all anoxic conditions, although results of various studies are often contradictory, which suggests that site-specific conditions are important parameters. So far, TBA degradation has not been shown under methanogenic conditions and it is currently widely accepted that TBA is a recalcitrant dead-end product of MTBE under these conditions. Reliable in situ degradation rates for MTBE and TBA under various geochemical conditions are not yet available. Furthermore, degradation pathways under anoxic conditions have not yet been elucidated. All pure cultures capable of MTBE or TBA degradation isolated so far use oxygen as terminal electron acceptor. In general, compared with hydrocarbons present in gasoline, fuel oxygenates biodegrade much slower, if at all. The presence of MTBE and related compounds in groundwater therefore frequently limits the use of in situ biodegradation as remediation option at gasoline-contaminated sites. Though degradation of MTBE and TBA in field studies has been reported under oxic

  5. Visible light assisted photocatalytic degradation of methyl orange using Ag/N-TiO₂ photocatalysts.

    Science.gov (United States)

    Wu, Deyong; Long, Mingce

    2012-01-01

    For the sake of efficient utilization of sunlight, Ag nanoparticles loaded N-doped TiO₂ photocatalysts (Ag/N-TiO₂) were successfully fabricated via a two-step method to make the best use of the respective advantages of noble metal loading and nonmetal doping. Ag/N-TiO₂ was characterized using XRD, XPS and UV-Vis DRS. Compared to TiO₂, the dramatic enhancement of the visible-light-induced photocatalytic degradation efficiency of Ag/N-TiO₂ obtained for the degradation of methyl orange should be attributed to the synergistic effect of N-doping and Ag-loading, including the good visible light absorption and the effective electron-hole separations. This demonstrates Ag/N-TiO₂ is a promising photocatalytic material for organic pollutant degradation under visible light irradiation.

  6. Stereochemical dependence of 3JCH coupling constants in 2-substituted 4-t-butyl-cyclohexanone and their alcohol derivatives.

    Science.gov (United States)

    Favaro, Denize C; Ducati, Lucas C; dos Santos, Francisco P; Contreras, Rubén H; Tormena, Cláudio F

    2011-12-22

    Theoretical and experimental studies on (3)J(C2H6eq) NMR spin-spin coupling constants in both the 2-X-4-t-butyl-cyclohexanone (X = H, CH(3), F, Cl, and Br) and in their alcohol derivatives series are reported. Results thus found are rationalized in terms of the transmission of the Fermi contact contribution to such couplings. To this end, dependencies of (3)J(C2H6eq) couplings versus the C(2)-C(1)-C(6) angle are compared in both series for equatorial and axial X orientations. The main trend is described in terms of the rear lobes interaction. Besides, for X = halogen atom in equatorial orientation a rather strong interaction between oxygen and halogen lone pairs is observed, and its influence on (3)J(C2H6eq) couplings is discussed and rationalized in terms of different Fermi contact transmission pathways.

  7. Solubilities of benzene, toluene and diphenyl in the t-butyl alcohol + water mixtures and hydrophobic interaction

    Institute of Scientific and Technical Information of China (English)

    邹立壮; 杨冠英; 韩布兴; 刘瑞麟; 阎海科

    1999-01-01

    The solubilitices of benzene, toluene and diphenyl in mixed solvents of t-butyl alcohol (TBA) and water at 283.15, 288.15, 293.15 and 298.15 K have been determined by spectrophotometry. The mole fraction of TBA [x (TBA)] in the mixed solvent are 0.000, 0.010, 0.020, 0.030, 0.040, 0.045, 0.050, 0.060, 0.080 and 0.100, respectively. The standard Gibbs energies of solution of benzene, toluene and diphenyl in the mixed solvent have also been calculated based on the solubility data. The hydrophobic interactions (HI) for the pairs of benzene-benzene, methane-benzene and methane-methane in the mixed solvent were calculated and discussed.

  8. HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES:SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY

    Institute of Scientific and Technical Information of China (English)

    Qi-song Shi; Xiang Hao; Carl Redshaw; Wen-hua Sun

    2013-01-01

    A series of nickel halides bearing 2,4-di-t-butyl-6-(quinolin-8-yliminomethyl) phenolate ligands was synthesized and characterized by IR spectroscopy and elemental analysis.Molecular structures of C1 (R =H,X =Br) and C2 (R =H,X =Cl) were further confirmed by single-crystal X-ray crystallographic studies,and revealed a distorted square planar geometry at nickel.Upon activation with diethylaluminum chloride (Et2AlCl),all nickel pre-catalysts displayed good catalytic activity [up to 9.3 × 105 g mol-1(Ni) h-1] for ethylene oligomerization with major dimerization.In the presence of methylaluminoxane (MAO),the nickel complex C1 was capable of ethylene polymerization under 3 MPa,and produced polyethylene products with narrow polydispersity (1.16-1.73) and molecular weights in the range of 2.6-4.95 kg/mol.

  9. Photocatalytic degradation of methyl orange by PbXO4 (X=Mo, W).

    Science.gov (United States)

    Zhiyong, Yu; Chaonan, Dong; Ruiying, Qiu; Lijin, Xu; Aihua, Zheng

    2015-01-15

    PbMoO4 and PbWO4 are prepared by the simple precipitation method in this work, they show the photocatalytic activities for the degradation of methyl orange in water under the UV light illumination. In the above photocatalytic degradation processes, methyl orange concentration decreases quickly, the total organic carbon (TOC) decreases slowly; inorganic ions (SO4(2-), NO3(-), NO2(-), NH4(+)) can be formed and measured by the ion chromatograph; the pH value in the systems decreases gradually; a small quantity of HO˙(-)·can be generated and measured by the terephthalic acid (TA) indirectly. In order to estimate the roles of active species during the above photocatalytic degradation processes, isopropanol, (NH4)2C2O4, and 1,4-benzoquinone as the scavengers for HO˙, h(+), O2˙(-) are introduced into the systems, respectively. Isopropanol and (NH4)2C2O4 are effective scavengers for active species HO˙ and h(+) respectively, but 1,4-benzoquinone is not a satisfactory scavenger in all cases to capture O2˙(-), at least in this work. At last, PbMoO4 and PbWO4 are characterized by nitrogen sorption, DRS, SEM, TEM and XRD.

  10. An Efficient Photocatalytic Degradation of Methyl Blue Dye by using Synthesised PbO Nanoparticles

    OpenAIRE

    Ashok V. Borhade; Dipak R. Tope; Bhagwat K. Uphade

    2012-01-01

    We report here the synthesis of visible light sensitive PbO and Ni doped PbO nanoparticles by hydrothermal method and characterized by UV-DRS, photoluminescence spectroscopy (PL), FTIR, X-ray diffraction (XRD), SEM, EDAX and TGA. Further an efficient approach has been developed for degradation of methyl blue (MB) in aqueous medium. The photodegradation of dye was monitored as a function of dye concentration, pH and catalyst amount has been determined. The reduction in the chemical oxygen dema...

  11. An Efficient Photocatalytic Degradation of Methyl Blue Dye by using Synthesised PbO Nanoparticles

    Directory of Open Access Journals (Sweden)

    Ashok V. Borhade

    2012-01-01

    Full Text Available We report here the synthesis of visible light sensitive PbO and Ni doped PbO nanoparticles by hydrothermal method and characterized by UV-DRS, photoluminescence spectroscopy (PL, FTIR, X-ray diffraction (XRD, SEM, EDAX and TGA. Further an efficient approach has been developed for degradation of methyl blue (MB in aqueous medium. The photodegradation of dye was monitored as a function of dye concentration, pH and catalyst amount has been determined. The reduction in the chemical oxygen demand (COD revealed the mineralization of dye along with colour removal.

  12. Photo catalytic degradation of methyl tert-Butyl Ether (MTBE) from contaminated water: complete mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Eslami, A.; Nasseri, S.; Maleki, A.; Aghvami, T.

    2009-07-01

    Methyl tert-butyl ether (MTBE) has been commercially used as an octane enhancer to replace tetraethyl lead in gasoline since 1979. The high mobility, water solubility, and resistance to natural attenuation associated with MTBE may result in contamination of ground and surface waters. In this investigation the degradation of aqueous MTBE at relatively high concentrations was studied by UV-vis/TiO{sub 2}/O{sub 2} photo catalytic process. The effect of important operational parameters such as ph, oxygen flow, catalyst loading, and irradiation time were also studied. (Author)

  13. Silver di-t-butyl phosphate, a useful reagent in the synthesis of phospholipids. Synthesis of mixed-acid phosphatidic acid and phosphatidyl glycerolphosphate

    NARCIS (Netherlands)

    Bonsen, P.P.M.; Haas, Gerard H. de

    1967-01-01

    The synthesis of silver di-t-butyl phosphate is described. Using this reagent, mixed-acid phosphatidic acid with one unsaturated fatty acid could be prepared by means of a reaction with a 1,2-diacyl glycerol-3-iodohydrin. The blocking groups could be removed easily with dry hydrogen chloride at low

  14. Isolation, Identification and Growth Characteristics of Four Tribenuron-methyl Degrading Bacterias

    Directory of Open Access Journals (Sweden)

    TIAN Shuang

    2014-10-01

    Full Text Available Four bacterias named B1, B2, B3 and B4 which were able to degrade tribenuron-methyl, were isolated from the soil of long term applied with tribenuron-methyl by enrichment culture. Based on physiological and biochemical characteristics and 16S rDNA sequence anal-ysis, the strain B1 was identified preliminarily as Pseudomonas aeruginosa, the strain B2 was identified preliminarily as Delftia sp., the strain B3 was identified preliminarily as Microbacterium sp., and the strain B4 was identified preliminarily as Alcaligenes sp.The effect of tempera-ture, initial pH, inoculation amount, initial concentration of tribenuron-methyl, medium volume, nitrogen source, carbon source and Mg 2+concentration on growth efficiencies was studied. The results showed that B1 optimal temperature was 35 ℃, the rest were 30 ℃. B3 optimal initial pH was 8.0, the others were 7.0. B1 and B3 optimal inoculation amount were 15%, B2 and B4 optimal inoculation amount were 10%.B3 optimal initial concentration of tribenuron-methyl was 100 mg· L-1, the other three were 200 mg· L -1. The four bacterias optimal medium volume all were 75 mL, optimal nitrogen source were ammonium nitrate and optimal carbon source were glucose. B2 optimal Mg 2+ concentra-tion was 100 mg·L -1, the others were 200 mg·L v. B1 and B4 optimal sodium chloride concentration were 20 g· L -1 while B2 could grow well from 5 g·L -1 to 30 g·L-1, B3 optimal sodium chloride concentration was 50 g·L -1. The results provide theoretical basis for using bacterias in situ bioremediation of soil pollution of tribenuron-methyl.

  15. Catalytic Reductive Degradation of Methyl Orange Using Air Resilient Copper Nanostructures

    Directory of Open Access Journals (Sweden)

    Razium Ali Soomro

    2015-01-01

    Full Text Available The study describes the application of oxidation resistant copper nanostructures as an efficient heterogeneous catalyst for the treatment of organic dye containing waste waters. Copper nanostructures were synthesized in an aqueous environment using modified surfactant assisted chemical reduction route. The synthesized nanostructures have been characterized by UV-Vis, Fourier transform infrared spectroscopy FTIR spectroscopy, Atomic force microscopy (AFM, Scanning Electron Microscopy (SEM, and X-ray diffractometry (XRD. These surfactant capped Cu nanostructures have been used as a heterogeneous catalyst for the comparative reductive degradation of methyl orange (MO in the presence of sodium borohydride (NaBH4 used as a potential reductant. Copper nanoparticles (Cu NPs were found to be more efficient compared to copper nanorods (Cu NRds with the degradation reaction obeying pseudofirst order reaction kinetics. Shape dependent catalytic efficiency was further evaluated from activation energy (EA of reductive degradation reaction. The more efficient Cu NPs were further employed for reductive degradation of real waste water samples containing dyes collected from the drain of different local textile industries situated in Hyderabad region, Pakistan.

  16. [Biosynthetic schwertmannite as catalyst in Fenton-like reactions for degradation of methyl orange].

    Science.gov (United States)

    Wang, Kuai-Bing; Fang, Di; Xu, Zhi-Hui; Shi, Ying; Zheng, Guan-Yu; Zhou, Li-Xiang

    2015-03-01

    Biosynthesized schwertmannite was used as catalyst in photo-Fenton-like reaction to facilitate the degradation of methyl orange (MO). Schwertmannite was synthesized through the oxidation of FeSO4 by Acidithiobacillus ferrooxidans LX5 cell suspension at an initial pH 2.5 and 28 degress C for 3 days and characterized using X-ray diffraction spectroscopy and scanning electron microscope. The oxidative degradation of MO in the photo-Fenton-like reaction was studied at different initial pH values of suspension, concentrations of H2O2 and dosages of catalyst. The results suggested that the biosynthetic schwertmannite showed a good catalytic activity in the MO degradation via *OH radical mechanism. Considerable degradation efficiency of MO was still obtained in approximately neutral condition or in the presence of high concentrations of chloride, sulfate and nitrate. This work demonstrated that the heterogeneous photo-Fenton-like reaction catalyzed by the biosynthetic schwertmannite is a promising advanced oxidation technology for the treatment of wastewater containing MO.

  17. Photo-Fenton-like degradation of azo dye methyl orange using synthetic ammonium and hydronium jarosite

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zhihui [Department of Chemistry, College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Liang, Jianru [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Zhou, Lixiang, E-mail: lxzhou@njau.edu.cn [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China)

    2013-01-05

    Highlights: Black-Right-Pointing-Pointer Hydronium and ammonium jarosite could catalyze the oxidation of methyl orange in photo-Fenton-like process. Black-Right-Pointing-Pointer The oxidation process is essentially heterogeneous, not homogeneous. Black-Right-Pointing-Pointer Hydronium jarosite has stronger reactivity than ammonium jarosite. - Abstract: Ammonium and hydronium jarosite were prepared by hydrothermal method with urea as the homogeneous precipitant. X-ray diffraction, field-emission scanning electron microscope, X-ray photoelectron spectrum, UV-vis spectra and fourier transform infrared spectrum were used to characterize the resulting products. The photodegradation efficiency of the prepared ammonium and hydronium jarosite was studied in a photo-Fenton-like process using methyl orange (MO) as target pollutant. The photocatalytic degradation of MO over synthetic ammonium and hydronium jarosite under various conditions, such as catalysts loading, H{sub 2}O{sub 2} concentration and initial pH, has been investigated. Results show that ammonium and hydronium jarosite have satisfactory photocatalysis effect in degradation of MO azo dye, and that the reactivity of hydronium jarosite toward the mineralization of MO was higher than that of ammonium jarosite. The novel ammonium and hydronium jarosite catalysts would be important for industrial applications due to their high photoactivity, little iron leaching and low cost.

  18. Anatase TiO{sub 2} hierarchical nanospheres with enhanced photocatalytic activity for degrading methyl orange

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Liqin; Xu, Wence [School of Materials Science and Engineering, Tianjin University, Tianjin, 300072 (China); Zhu, Shengli, E-mail: slzhu@tju.edu.cn [School of Materials Science and Engineering, Tianjin University, Tianjin, 300072 (China); Tianjin Key Laboratory of Composite and Functional Materials, Tianjin, 300072 (China); Cui, Zhenduo [School of Materials Science and Engineering, Tianjin University, Tianjin, 300072 (China); Yang, Xianjin [School of Materials Science and Engineering, Tianjin University, Tianjin, 300072 (China); Tianjin Key Laboratory of Composite and Functional Materials, Tianjin, 300072 (China); Inoue, Akihisa [School of Materials Science and Engineering, Tianjin University, Tianjin, 300072 (China); International Institute of Green Materials, Josai International University, Togane, 283-8555 (Japan)

    2016-02-15

    Anatase TiO{sub 2} hierarchical nanospheres were synthesized through a simple way combining dealloying and hydrothermal methods. The photocatalytic activity of the obtained products and Degussa P25 were evaluated by the degradation of methyl orange (MO) aqueous solution at different initial pH values and concentrations. The anatase TiO{sub 2} hierarchical nanospheres exhibited excellent photocatalytic activity for the degradation of methyl orange under ultraviolet–visible light irradiation. The photocatalytic efficiency of the anatase TiO{sub 2} increased with the decrease of pH at first then decreased and it also decreased with the increase of MO concentration. The superior photocatalytic performance of anatase TiO{sub 2} hierarchical nanospheres is attributed to its crystal phase, microstructure, and particularly surface acidity. The enhancement of surface acidity reduces the electron–hole pair recombination, and further increases the photocatalytic efficiency. - Highlights: • Anatase TiO{sub 2} nanospheres was prepared by chemical dealloying method. • The anatase TiO{sub 2} nanospheres exhibited good photocatalytic activity. • Sulfate ions adsorbed on TiO{sub 2} was beneficial for the photocatalytic performance.

  19. Identification of a Marine Bacillus Strain C5 and Parathion-Methyl Degradation Characteristics of the Extracellular Esterase B1

    Directory of Open Access Journals (Sweden)

    Jianhua Hao

    2014-01-01

    Full Text Available A bacterial strain C5 that can produce new type of marine esterase was isolated and screened from marine sludge. According to 16S rRNA sequence analysis and physiological and biochemical experiments, the strain was identified as Bacillus subtilis. A single isozyme with a molecular weight of 86 kDa was observed by SDS-PAGE and native-PAGE. On this basis, the mechanism of esterase B1 secreted by strain C5 degrading parathion-methyl was explored, and the effects of temperature and pH on the degradation rate were investigated. From the results, p-nitrophenol was one of the degradation products of B1 degrading parathion-methyl, and the best degradation effect could be achieved at the temperature of 40°C and the neutral pH value.

  20. Biochemical Characterization of 3-Methyl-4-nitrophenol degradation in Burkholderia sp. Strain SJ98

    Directory of Open Access Journals (Sweden)

    Jun eMin

    2016-05-01

    Full Text Available Several strains have been reported to grow on 3-methyl-4-nitrophenol (3M4NP, the primary breakdown product of the excessively used insecticide fenitrothion. However, the microbial degradation of 3M4NP at molecular and biochemical levels remains unknown. Here, methyl-1,4-benzoquinone (MBQ and methylhydroquinone (MHQ,rather than catechol proposed previously, were identified as the intermediates before ring cleavage during 3M4NP degradation by Burkholderia sp. strain SJ98. Real-time quantitative PCR analysis indicated that the pnpABA1CDEF cluster involved in para-nitrophenol (PNP and 2-chloro-4-nitrophenol (2C4NP catabolism was also likely responsible for 3M4NP degradation in this strain. Purified PNP 4-monooxygenase (PnpA is able to catalyze the monooxygenation of 3M4NP to MBQ and exhibited an apparent Km value of 20.3±2.54 μM for 3M4NP, and pnpA is absolutely necessary for the catabolism of 3M4NP by gene knock-out and complementation. PnpB, a 1,4-benzoquinone reductase catalyzes the reduction of MBQ to MHQ, and also found to enhance PnpA activity in vitro in the conversion of 3M4NP to MBQ. By sequential catalysis assays, PnpCD, PnpE and PnpF were likely involved in the lower pathway of 3M4NP catabolism. Although NpcCD, NpcE and NpcF are able to catalyze the sequential conversion of MHQ in vitro, these enzymes are unlikely involved in 3M4NP catabolism because their coding genes were not upregulated by 3M4NP induction in vivo. These results revealed that the enzymes involved in PNP and 2C4NP catabolism were also responsible for 3M4NP degradation in strain SJ98. This fills a gap in our understanding of the microbial degradation of 3M4NP at molecular and biochemical levels and also provides another example to illustrate the adaptive flexibility in microbial catabolism for structurally similar compounds.

  1. Interfacial interaction between methyl parathion-degrading bacteria and minerals is important in biodegradation.

    Science.gov (United States)

    Zhao, Gang; Huang, Qiaoyun; Rong, Xingmin; Cai, Peng; Liang, Wei; Dai, Ke

    2014-02-01

    In the present study, the influence of kaolinite and goethite on microbial degradation of methyl parathion was investigated. We observed that the biodegradation process was improved by kaolinite and depressed by goethite. Calorimetric data further showed that the metabolic activities of degrading cells (Pseudomonas putida) were enhanced by the presence of kaolinite and depressed by the presence of goethite. A semipermeable membrane experiment was performed and results supported the above observations: the promotive effect of kaolinite and the inhibition of goethite for microbial degradation was not found when the bacteria was enclosed by semipermeable membrane and had no direct contact with these minerals, suggesting the important function of the contact of cellular surfaces with mineral particles. The relative larger particles of kaolinite were loosely attached to the bacteria. This attachment made the cells easy to use the sorbed substrate and then stimulated biodegradation. For goethite, small particles were tightly bound to bacterial cells and limited the acquisition of substrate and nutrients, thereby inhibiting biodegradation. These results indicated that interfacial interaction between bacterial cells and minerals significantly affected the biodegradation of pesticides.

  2. Study of Degradation Kinetics of Parathion Methyl On Mixed Nanocrystalline Titania-Zirconium and Titania-Cerium Oxides

    Science.gov (United States)

    Kuráň, Pavel; Pšenička, Martin; Šťastný, Martin; Benkocká, Monika; Janoš, Pavel

    2016-10-01

    The unique surface properties of some nanocrystalline metal oxides and their application for removal of various toxic compounds were reported in early 1990s. Recently, a reliable method for the preparation of reactive cerium dioxide sorbent and its application for degradation of the organophosphate pesticides, such as parathion methyl, chlorpyrifos, dichlofenthion, fenchlorphos, and prothiofos, as well as of some chemical warfare agents-nerve gases soman and O-ethyl S-[2-(diisopropylamino) ethyl] methylphosphonothioate (VX) was published. This paper reports on the kinetics study of degradation of parathion methyl as a representative organophosphate on nanocrystalline metal oxides TiO2, ZrO2, CeO2 and their mixtures in different molar ratios of particular elements. The tested sorbents except of CeO2 were prepared by different methods (e.g. sol-gel, precipitation) in cooperation with Institute of Inorganic Chemistry (Rez, Czech Republic). The degradation kinetics of parathion methyl on tested sorbents was followed by HPLC equipped with diode array detector. The basic kinetics parameters (half-lives of parathion methyl degradation, rate constants of degradation product formation) were calculated for each sorbent from Weber-Morris equation of 1st order diffusion kinetic model. The results proved the ability of prepared sorbents to degrade parathion methyl under formation of 4-nitrophenol as the main degradation product. The most efficient sorbents were TiCe (2:8), TiCe (1:1), TiCe (0:1) (50-70 %) followed by TiZr (1:1), TiCe (8:2), TiZr (8:2), TiZr (2:8) (20-30%) and TiO2, ZrO2 (less than 5 %).

  3. Sonocatalytic degradation of methyl orange in the presence of (nanometer and ordinary) anatase TiO2 powders

    Institute of Scientific and Technical Information of China (English)

    WANG Jun; GUO Bao-dong; ZHANG Zhao-hong; ZHANG Xiang-dong; WU Jing; LI Hong

    2005-01-01

    The nanometer and ordinary anatase titanium dioxide(TiO2 ) powders were adopted as the sonocatalysts for the degradation of methyl orange used as a model compound for the first time. It was found that the sonocatalytic degradation effect of methyl orange in the presence of TiO2 powder were much better than that without TiO2, but the sonocatalytic activity of the nanometer anatase TiO2 particle was obviously higher than that of ordinary anatase TiO2 particle. Although there are many factors influencing sonocatalytic degradation of methyl orange, the experimental results showed that the best degradation ratio of methyl orange could be obtained when the experimental conditions were: initial concentration 15 mg/L, nanometer anatase TiO2 adding amount 750 mg/L, ultrasonic frequency 40 kHz, output power 50 W, pH = 3.0 and temperature 40℃ within 150 min. In addition, the catalytic activity of reused nanometer anatase TiO2 catalyst was also studied and found to decline gradually comparing with initial nanometer anatase TiO2 catalyst. All experiments indicated that the method of the sonocatalytic degradation of organic pollutants in the presence of TiO2 powder was an advisable choice for non- or lowtransparent organic wastewaters.

  4. Twofold role of calcined hydrotalcites in the degradation of methyl parathion pesticide.

    Science.gov (United States)

    Sampieri, Alvaro; Fetter, Geolar; Villafuerte-Castrejon, María Elena; Tejeda-Cruz, Adriana; Bosch, Pedro

    2011-01-01

    Methyl parathion (MP) is a very toxic organophosphate pesticide used as a non-systematic insecticide and acaricide on many corps. As MP and its by-products are highly toxic, they have to be retained to avoid pollution of rivers and lakes. Highly efficient sorbents are hydrotalcites (HTs) (or anionic clays). We have correlated the degradation of an aqueous solution of MP at room temperature, with the basicity of the adsorbing materials. It was found that the metal composition of hydrotalcites determines both the surface electronic properties (basic or acidic) and the sorption capacity. Depending on the basic strength, some calcined hydrotalcites can catalyze the transformation of MP to p-nitrophenol (p-NP) and retain its by-products. Such a process has the advantage of being able to be carried out at room temperature and at the pH of the pesticide solution.

  5. Evaluation of integrated anaerobic-aerobic biofilm reactor for degradation of azo dye methyl orange.

    Science.gov (United States)

    Murali, V; Ong, Soon-An; Ho, Li-Ngee; Wong, Yee-Shian

    2013-09-01

    This study was to investigate the mineralization of wastewater containing methyl orange (MO) in integrated anaerobic-aerobic biofilm reactor with coconut fiber as bio-material. Different aeration periods (3h in phase 1 and 2; 3, 6 and 15 h in phase 3; 24 h in phase 4 and 5) in aerobic chamber were studied with different MO concentration 50, 100, 200, 200 and 300 mg/L as influent from phase 1-5. The color removals estimated from the standard curve of dye versus optical density at its maximum absorption wavelength were 97%, 96%, 97%, 97%, and 96% and COD removals were 75%, 72%, 63%, 81%, and 73% in phase 1-5, respectively. The MO decolorization and COD degradation followed first-order kinetic model and second-order kinetic model, respectively. GC-MS analysis indicated the symmetrical cleavage of azo bond and the reduction in aromatic peak ensured the partial mineralization of MO.

  6. Twofold role of calcined hydrotalcites in the degradation of methyl parathion pesticide

    Directory of Open Access Journals (Sweden)

    Alvaro Sampieri

    2011-02-01

    Full Text Available Methyl parathion (MP is a very toxic organophosphate pesticide used as a non-systematic insecticide and acaricide on many corps. As MP and its by-products are highly toxic, they have to be retained to avoid pollution of rivers and lakes. Highly efficient sorbents are hydrotalcites (HTs (or anionic clays. We have correlated the degradation of an aqueous solution of MP at room temperature, with the basicity of the adsorbing materials. It was found that the metal composition of hydrotalcites determines both the surface electronic properties (basic or acidic and the sorption capacity. Depending on the basic strength, some calcined hydrotalcites can catalyze the transformation of MP to p-nitrophenol (p-NP and retain its by-products. Such a process has the advantage of being able to be carried out at room temperature and at the pH of the pesticide solution.

  7. The thermal degradation of Poly(methyl methacrylate/silicon carbide nanocomposites

    Directory of Open Access Journals (Sweden)

    Popović Ivanka G.

    2002-01-01

    Full Text Available The thermal stability of poly(methyl methacrylate (PMMA and silicon carbide (SiC composites was studied by thermogravimetry. The influence of particle size, SiC structural modification and particle specific surface was analyzed. It was established that particle size had the greatest influence on PMMA/SiC thermal stability and that the most stable composites were those with the smallest particle diameter, i.e the largest particle specific surface. The values of the thermal degradation activation energy indicated that in some cases particle deagglomeration probably did occur which enabled polymer-filler nanoscale interaction and indicated that the system PMMA/SiC could form nanocomposites.

  8. Isolation and Initial Characterization of A Pure Cultures Capable to Degradation Methyl tert- Butyl Ether (MTBE

    Directory of Open Access Journals (Sweden)

    A Nikpey

    2006-07-01

    Full Text Available Methyl tert-butyl ether (MTBE, a gasoline octane enhancer, was introduced as a substitute for lead tetraethyl over 30 years ago. Widespread use of MTBE in gasoline, has introduced MTBE into the environment compartments, mostly into the under ground and surface water and water as a second most frequently detected contaminant. In this study, we have isolated pure cultures from bacterial consortium capable to use MTBE as a sole carbon and energy source. MTBE biodegradation rate was measured in headspace by gas chromatography. Initial liner rates of biodegradation by Pinpoint and white strains were found 2.9 mg and 3 mg MTBE hˉ1 gˉ1 wet biomass, respectively. The results of 16S rDNA PCR disclosed similarities in the banding patterns between the cultures, and the known degrading strain PM1. The results of this study suggest promising perspectives for engineering the in situ bioremediation of MTBE.

  9. Degradation of aqueous methyl tert-butyl ether by photochemical, biological, and their combined processes

    Directory of Open Access Journals (Sweden)

    Azadeh Asadi

    2006-01-01

    Full Text Available The degradation of aqueous methyl tert-butyl ether (MTBE at relatively high concentrations was investigated by various photo-induced oxidation processes such as UV/H2O2 and UV/TiO2 as well as biological processes and their combination. It was shown that the degradation of MTBE by UV/H2O2 and TiO2 photocatalytic followed a first-order model with apparent rate constant of 1.31×10−1 and 1.21×10−2 min-1, respectively. It was observed that UV/H2O2/TiO2 process did not have any advantages over each of the other processes alone. The biodegradation of methyl tert-butyl ether (MTBE was evaluated using aerobic mixed culture with three different approaches, including ultimate biological oxygen demand (BODU assessment, nonacclimated, and acclimated mixed cultures. The apparent rate constant for the biodegradation of MTBE by nonacclimated mixed culture was 4.36×10−2 day-1. It was shown that the acclimatization of the mixed cultures enhanced the rate of biodegradation of MTBE to 3.24×10−1mg L-1h-1. Finally, the effects of the photocatalytic pretreatment of aqueous MTBE on its subsequent biological treatment were studied. It was observed that the rate of bioreaction was not enhanced and the photocatalytic pretreatment had adverse effects on its biological treatment so that the apparent rate constant decreased to 2.83×10−1 mg L-1h-1.

  10. Rapid methyl orange degradation using porous ZnO spheres photocatalyst.

    Science.gov (United States)

    Tripathy, Nirmalya; Ahmad, Rafiq; Kuk, Hyeon; Lee, Dae Hoon; Hahn, Yoon-Bong; Khang, Gilson

    2016-08-01

    Porous zinc oxide (ZnO) spheres were synthesized by facile low temperature solution route. The as-synthesized porous ZnO spheres were characterized in detail in terms of their morphological, structural, optical and photocatalytic properties using field-emission scanning electron microscopy (FESEM, equipped with energy dispersive spectroscopy (EDS)), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), X-ray diffractometer (XRD), UV-visible spectroscopy and Raman-scattering measurements. Nitrogen adsorption-desorption analysis was performed to determine pore size distribution from the adsorption isotherm curves using the Barrett-Joyner-Halenda (BJH) method. Morphological and structural characterizations showed porous nature of ZnO spheres with high surface area, good crystallinity, wurtzite hexagonal phase and good optical features. Next, ZnO spheres were studied as photocatalyst for photodegradation of harmful dye, methyl orange (MO). Under ultraviolet light irradiation, the decrease in MO dye concentration was monitored by UV-visible spectroscopy at different time intervals until the dye was completely degraded to colorless end product. Rapid MO dye decomposition was observed with a degradation rate of ~96.3% within the initial 120min, which is attributed to the porous nature, large specific surface area (114.6m(2)g(-1)), narrow pore size distribution (~2.5 to 25nm) evaluated from N2 adsorption-desorption isotherms analysis and excellent electron accepting features of the engineered porous ZnO spheres. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Photocatalytic degradation of methyl orange over ITO/CdS/ZnO interface composite films

    Institute of Scientific and Technical Information of China (English)

    WEI Shouqiang; SHAO Zhongcai; LU Xudong; LIU Ying; CAO Linlin; HE Yan

    2009-01-01

    ITO/CdS/ZnO interface composite films were successfully prepared by subsequent electrodeposition of CdS and ZnO onto indium tin oxide (ITO) glass substrates. The obtained ITO/CdS/ZnO composite films were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-Vis spectroscopy. The photocatalytic activity of ITO/CdS/ZnO composite films were investigated using methyl orange (MO) as a model organic compound under UV light irradiation. The influence of operating parameters on MO degradation including initial concentration of MO, pH value of solution, and inorganic anion species over the composite films were examined. A blue shift of absorption threshold was observed for the ITO/CdS/ZnO film in comparison with ITO/ZnO film. ITO/CdS/ZnO composite films prepared under specific conditions showed a higher photocatalytic activity than that of ITO/ZnO films. It was also found that the photocatalytic degradation of MO on the composite filing followed pseudo-first order kinetics.

  12. Photocatalytic degradation of methyl orange over ITO/Cds/ZnO interface composite films.

    Science.gov (United States)

    Wei, Shouqiang; Shao, Zhongcai; Lu, Xudong; Liu, Ying; Cao, Linlin; He, Yan

    2009-01-01

    ITO/CdS/ZnO interface composite films were successfully prepared by subsequent electrodeposition of CdS and ZnO onto indium tin oxide (ITO) glass substrates. The obtained ITO/CdS/ZnO composite films were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-Vis spectroscopy. The photocatalytic activity of ITO/CdS/ZnO composite films were investigated using methyl orange (MO) as a model organic compound under UV light irradiation. The influence of operating parameters on MO degradation including initial concentration of MO, pH value of solution, and inorganic anion species over the composite films were examined. A blue shift of absorption threshold was observed for the ITO/CdS/ZnO film in comparison with ITO/ZnO film. ITO/CdS/ZnO composite films prepared under specific conditions showed a higher photocatalytic activity than that of ITO/ZnO films. It was also found that the photocatalytic degradation of MO on the composite films followed pseudo-first order kinetics.

  13. Repeated oxidative degradation of methyl orange through bio-electro-Fenton in bioelectrochemical system (BES).

    Science.gov (United States)

    Ling, Ting; Huang, Bin; Zhao, Mingxing; Yan, Qun; Shen, Wei

    2016-03-01

    Composite Fe2O3/ACF electrode facilitated methyl orange (MO) oxidative degradation using bio-electro-Fenton in bioelectrochemical system (BES) was investigated. Characterized by both XPS and FT-IR techniques, it was found that the composite Fe2O3/ACF electrode with highest Fe loading capacity of 11.02% could be prepared after the carbon felt was oxidized with nitric acid. Moreover, hydrogen peroxide production reached steadily at 88.63 μmol/L with the external resistance as 100 Ω, cathodic aeration rate at 750 mL/min, and the pH of the bio-electro-Fenton system adjusted to 2. Significantly, not only the electrochemical profiles of the BES reactor as electrochemical impedance spectroscopy (EIS) was bettered, but the MO oxidative degradation could be accomplished for eight repeated batches, with the MO removal efficiency varied slightly from 73.9% to 86.7%. It indicated that the bio-electro-Fenton might be a promising eco-friendly AOP method for Azo-dye wastewater treatment.

  14. Photocatalysis using zero-valent nano-copper for degrading methyl orange under visible light irradiation

    Science.gov (United States)

    Liú, Dan; Wang, Guoqiang; Liŭ, Dan; Lin, Junhong; He, Yingqiao; Li, Xiangru; Li, Ziheng

    2016-03-01

    As one of zero-valent transition metals, nano-copper was synthesized by a simple chemical reduction route and its photocatalytic activity was appraised by the degradation rate of methyl orange (MO) in aqueous solution under irradiation of a three-band fluorescent lamp. The results showed that nano-copper possessed visible-light photocatalytic activity. The finite-difference time-domain (FDTD) method was used to simulate the electric field distribution of nano-copper. From the results of simulation, it found that there was an enhancement electric field in course of light absorption on the surface of nano-copper, different morphology resulted in a diverse electric field distribution. Enhancement electric field intensity decided the visible-light photocatalytic activity of nano-copper. So the activity was affected by the morphology of nano-copper, as the size reduced and surface roughness increased, could be enhanced. It did be worth noting that the nanoscale of copper played the fatal decisive role for whether copper has the ability to degrade MO. So As-prepared nano-copper may be a novel visible-light photocatalytic material to treat organic pollution.

  15. Isolation of a selected microbial consortium capable of degrading methyl parathion and p-nitrophenol from a contaminated soil site.

    Science.gov (United States)

    Pino, Nancy J; Dominguez, Maria C; Penuela, Gustavo A

    2011-01-01

    A bacterial consortium with the ability to degrade methyl parathion and p-nitrophenol, using these compounds as the only carbon source, was obtained by selective enrichment in a medium with methyl parathion. Samples were taken from Moravia, Medellin; an area that is highly contaminated, owing to the fact that it was used as a garbage dump from 1974 to 1982. Acinetobacter sp, Pseudomonas putida, Bacillus sp, Pseudomonas aeruginosa Citrobacter freundii, Stenotrophomonas sp, Flavobacterium sp, Proteus vulgaris, Pseudomonas sp, Acinetobacter sp, Klebsiella sp and Proteus sp were the microorganisms identified within the consortium. In culture, the consortium was able to degrade 150 mg L⁻¹ of methyl-parathion and p-nitrophenol in 120 h, but after adding glucose or peptone to the culture, the time of degradation decreased to 24 h. In soil, the consortium was also able to degrade 150 mg L⁻¹ of methyl parathion in 120 h at different depths and also managed to decrease the toxicity.

  16. On the degelation of networks – Case of the radiochemical degradation of methyl methacrylate – ethylene glycol dimethacrylate copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Richaud, Emmanuel; Gilormini, Pierre; Verdu, Jacques [Arts et Métiers ParisTech, CNRS, PIMM UMR 8006, 151 bd de l’Hôpital, 75013 Paris (France)

    2016-05-18

    Methyl methacrylate networks were synthetized and submitted to radiochemical degradation. Ageing was monitored by means of sol-gel analysis and glass transition temperature measurements. Networks were shown to undergo exclusively chain scission process leading to the degelation of network. The critical conversion degree corresponding to degelation (loss of all elastically active chains) is discussed regarding a statistical theory.

  17. Degradation mechanism of Methyl Orange by electrochemical process on RuO(x)-PdO/Ti electrode.

    Science.gov (United States)

    Du, Lin; Wu, Jin; Qin, Song; Hu, Changwei

    2011-01-01

    The electrochemical degradation of Methyl Orange in 0.1 M NaCl solution over RuO(x)-PdO/Ti anode was investigated. Chemical oxygen demand (COD), ion chromatography (IC), Fourier Transform Infrared Spectroscopy (FTIR) and Gas chromatography-mass spectrometry (GC-MS) were employed to detect the intermediates formed during the electrochemical degradation. In the present reaction system, Methyl Orange could be effectively degraded. After 1 h treatment, the discoloration could reach 97.9% with COD removal of 57.6%. The results indicated that in the presence of chloride, the electrolysis was able to oxidise the dye with partial mineralisation of carbon, nitrogen and sulfur into CO(2), NO(-)(3) and SO(2-)(4), respectively. After 8 h electrolysis, 62% of sulfur contained in Methyl Orange was transformed to SO(4)(2-), and 17.6% of nitrogen changed to NO(3)(-). The intermediates during electroprocess were detected to be low molecular weight compounds, chlorinated compounds, derivatives of benzene and long chain alkanes. Based on these data, a possible degradation mechanism of Methyl Orange was proposed.

  18. Photocatalytic degradation of methyl orange by nano-TiO_2 thin films prepared by RF magnetron sputtering

    Institute of Scientific and Technical Information of China (English)

    Fanming Meng; Ling Cao; Xueping Song; Zhaoqi Sun

    2009-01-01

    Nano-TiO_2 thin films are deposited by radio frequency (RF) magnetron sputtering using TiO_2 ceramic target and characterized by X-ray diffractometer,atomic force microscope,and ultraviolet-visible spectrophotometer.The photocatalytic activity is evaluated by light-induced degradation of methyl orange solutions (5,10,and 20 ppm) using a high pressure mercury lamp as the light source.The film is amorphous,and its energy gap is 3.02 Ev.The photocatalytic degradation of methyl orange solution is the first-order reaction and the apparent reaction rate constants are 0.00369,0.0024,and 0.00151 for the methyl orange solution concentrations of 5,10,and 20 ppm,respectively.

  19. Influence of inorganic anions and organic additives on photocatalytic degradation of methyl orange with supported polyoxometalates as photocatalyst

    Institute of Scientific and Technical Information of China (English)

    WANG Yajun; LU Kecheng; FENG Changgen

    2013-01-01

    A novel supported polyoxometalate (POM),phosphotungstic acid immobilized into yttrium-doped TiO2 (HPW-Y-TiO2)nano photocatalyst was prepared via sol-gel and impregnation method.The samples were characterized using Fourier transform infrared spectroscopy (FT-IR),X-ray diffraction (XRD) and N2 absorption-desorption analysis.The results showed that the supported POM exhibited Keggin structure and anatase phase with large BET surface area.The influences of inorganic anions and organic additives on the photocatalytic degradation of azo dye methyl orange with HPW-Y-TiO2 as photocatalyst under UV light (λ≥365 um)were investigated.Results showed that inorganic anions Cl-,SO42-,CO32-and NO3-had inhibition effect on the degradation of methyl orange.A great enhancement of degradation rate was obtained while H2O2 and ethyl alcohol were applied.The degradation rates improved with the increase of H2O2 concentration.The optimum additive amount of ethyl alcohol was 0.5 mol/L.The possible mechanisms of the effects of additives on methyl orange degradation were discussed.

  20. Degradation of methyl orange by ozone in the presence of ferrous and persulfate ions in a rotating packed bed.

    Science.gov (United States)

    Ge, Deming; Zeng, Zequan; Arowo, Moses; Zou, Haikui; Chen, Jianfeng; Shao, Lei

    2016-03-01

    This work investigated the degradation of methyl orange by ozone in the presence of ferrous and persulfate ions (O3/Fe(2+)/S2O8(2-)) in a rotating packed bed. The effects of various operating parameters such as initial pH, rotational speed, gas-liquid ratio, ozone inlet concentration and reaction temperature on the degradation rate of methyl orange were studied with an aim to optimize the operation conditions. Results reveal that the degradation rate increased with an increase in rotational speed, gas-liquid ratio and ozone inlet concentration, and reached a maximum at 25 °C and initial pH 4. Contrast experiments involving ozone and ferrous ions (O3/Fe(2+)) were also carried out, and the results show approximately 10% higher degradation rate and COD removal in the O3/Fe(2+)/S2O8(2-) process than in the O3/Fe(2+) process. Additionally, the intermediates of the degradation process were analyzed to ascertain the degradation products.

  1. The degradation mechanism of methyl orange under photo-catalysis of TiO2.

    Science.gov (United States)

    Yu, Lihong; Xi, Jingyu; Li, Ming-De; Chan, Hung Tat; Su, Tao; Phillips, David Lee; Chan, Wai Kin

    2012-03-14

    The properties of photo-generated reactive species, holes and electrons in bulk TiO(2) (anatase) film and nano-sized TiO(2) were studied and their effects towards decomposing pollutant dye methyl orange (MO) were compared by transient absorption spectroscopies. The recombination of holes and electrons in nano-sized TiO(2) was found to be on the microsecond time scale consistent with previous reports in the literature. However, in bulk TiO(2) film, the holes and electrons were found to be on the order of picoseconds due to ultra fast free electrons. The time-correlated single-photon counting (TCSPC) technique combined with confocal fluorescence microscopy revealed that the fluorescence intensity of MO is at first enhanced noticeably by TiO(2) under UV excitation and soon afterwards weakened dramatically, with the lifetime prolonged. Photo-generated holes in nano-sized TiO(2) can directly oxidize MO on the time scale of nanoseconds, while free electrons photo-generated in bulk TiO(2) film can directly inject into MO on the order of picoseconds. Through cyclic voltammetry measurements, it was found that MO can be reduced at -0.28 V and oxidized at 1.4 V (vs. SCE) and this provides thermodynamic evidence for MO to be degraded by electrons and holes in TiO(2). Through comparison of the hole-scavenging effect of MO and water, it was found that in polluted water when MO is above 1.6 × 10(-4) M, the degradation is mainly due to a direct hole oxidation process, while below 1.6 × 10(-4) M, hydroxyl oxidation competes strongly and might exceed the hole oxidation.

  2. Degradation of methyl bromide and methyl chloride in soil microcosms: Use of stable C isotope fractionation and stable isotope probing to identify reactions and the responsible microorganisms

    Science.gov (United States)

    Miller, L.G.; Warner, K.L.; Baesman, S.M.; Oremland, R.S.; McDonald, I.R.; Radajewski, S.; Murrell, J.C.

    2004-01-01

    Bacteria in soil microcosm experiments oxidized elevated levels of methyl chloride (MeCl) and methyl bromide (MeBr), the former compound more rapidly than the latter. MeBr was also removed by chemical reactions while MeCl was not. Chemical degradation dominated the early removal of MeBr and accounted for more than half of its total loss. Fractionation of stable carbon isotopes during chemical degradation of MeBr resulted in a kinetic isotope effect (KIE) of 59 ?? 7???. Soil bacterial oxidation dominated the later removal of MeBr and MeCl and was characterized by different KIEs for each compound. The KIE for MeBr oxidation was 69 ?? 9??? and the KIE for MeCl oxidation was 49 ?? 3???. Stable isotope probing revealed that different populations of soil bacteria assimilated added 13C-labeled MeBr and MeCl. The identity of the active MeBr and MeCl degrading bacteria in soil was determined by analysis of 16S rRNA gene sequences amplified from 13C-DNA fractions, which identified a number of sequences from organisms not previously thought to be involved in methyl halide degradation. These included Burkholderia , the major clone type in the 13C-MeBr fraction, and Rhodobacter, Lysobacter and Nocardioides the major clone types in the 13C-MeCl fraction. None of the 16S rRNA gene sequences for methyl halide oxidizing bacteria currently in culture (including Aminobacter strain IMB-1 isolated from fumigated soil) were identified. Functional gene clone types closely related to Aminobacter spp. were identified in libraries containing the sequences for the cmuA gene, which codes for the enzyme known to catalyze the initial step in the oxidation of MeBr and MeCl. The cmuA gene was limited to members of the alpha-Proteobacteria whereas the greater diversity demonstrated by the 16S rRNA gene may indicate that other enzymes catalyze methyl halide oxidation in different groups of bacteria. Copyright ?? 2004 Elsevier Ltd.

  3. Response of anaerobes to methyl fluoride, 2-bromoethanesulfonate and hydrogen during acetate degradation

    Institute of Scientific and Technical Information of China (English)

    Liping Hao; Fan Lü; Lei Li; Liming Shao; Pinjing He

    2013-01-01

    To use the selective inhibition method for quantitative analysis of acetate metabolism in methanogenic systems,the responses of microbial communities and metabolic activities,which were involved in anaerobic degradation of acetate,to the addition of methyl fluoride (CH3F),2-bromoethanesulfonate (BES) and hydrogen were investigated in a thermophilic batch experiment.Both the methanogenic inhibitors,i.e.,CH3F and BES,showed their effectiveness on inhibiting CH4 production,whereas acetate metabolism other than acetoclastic methanogenesis was stimulated by BES,as reflected by the fluctuated acetate concentration.Syntrophic acetate oxidation was thermodynamically blocked by hydrogen (H2),while H2-utilizing reactions as hydrogenotrophic methanogencsis and homoacetogenesis were correspondingly promoted.Results of PCR-DGGE fingerprinting showed that,CH3F did not influence the microbial populations significantly.However,the BES and hydrogen notably altered the bacterial community structures and increased the diversity.BES gradually changed the methanogenic community structure by affecting the existence of different populations to different levels,whilst H2 greatly changed the abundance of different methanogenic populations,and induced growth of new species.

  4. Response of anaerobes to methyl fluoride, 2-bromoethanesulfonate and hydrogen during acetate degradation.

    Science.gov (United States)

    Hao, Liping; Lü, Fan; Li, Lei; Shao, Liming; He, Pinjing

    2013-05-01

    To use the selective inhibition method for quantitative analysis of acetate metabolism in methanogenic systems, the responses of microbial communities and metabolic activities, which were involved in anaerobic degradation of acetate, to the addition of methyl fluoride (CH3F), 2-bromoethanesulfonate (BES) and hydrogen were investigated in a thermophilic batch experiment. Both the methanogenic inhibitors, i.e., CH3F and BES, showed their effectiveness on inhibiting CH4 production, whereas acetate metabolism other than acetoclastic methanogenesis was stimulated by BES, as reflected by the fluctuated acetate concentration. Syntrophic acetate oxidation was thermodynamically blocked by hydrogen (H2), while H2-utilizing reactions as hydrogenotrophic methanogenesis and homoacetogenesis were correspondingly promoted. Results of PCR-DGGE fingerprinting showed that, CH3F did not influence the microbial populations significantly. However, the BES and hydrogen notably altered the bacterial community structures and increased the diversity. BES gradually changed the methanogenic community structure by affecting the existence of different populations to different levels, whilst H2 greatly changed the abundance of different methanogenic populations, and induced growth of new species.

  5. Magnetic Scanometric DNA Microarray Detection of Methyl Tertiary Butyl Ether Degrading Bacteria for Environmental Monitoring

    Science.gov (United States)

    Chan, Mei-Lin; Jaramillo, Gerardo; Hristova, Krassimira R.; Horsley, David A.

    2010-01-01

    A magnetoresistive biosensing platform based on a single magnetic tunnel junction (MTJ) scanning probe and DNA microarrays labeled with magnetic particles has been developed to provide an inexpensive, sensitive and reliable detection of DNA. The biosensing platform was demonstrated on a DNA microarray assay for quantifying bacteria capable of degrading methyl tertiary-butyl ether (MTBE), where concentrations as low as 10 pM were detectable. Synthetic probe bacterial DNA was immobilized on a microarray glass slide surface, hybridized with the 48 base pair long biotinylated target DNA and subsequently incubated with streptavidin-coated 2.8 μm diameter magnetic particles. The biosensing platform then makes use of a micron-sized MTJ sensor that was raster scanned across a 3 mm by 5 mm glass slide area to capture the stray magnetic field from the tagged DNA and extract two dimensional magnetic field images of the microarray. The magnetic field output is then averaged over each 100 μm diameter DNA array spot to extract the magnetic spot intensity, analogous to the fluorescence spot intensity used in conventional optical scanners. The magnetic scanning result is compared with results from a commercial laser scanner and particle coverage optical counting to demonstrate the dynamic range and linear sensitivity of the biosensing platform as a potentially inexpensive, sensitive and portable alternative for DNA microarray detection for field applications. PMID:20889328

  6. Enhanced cometabolic degradation of methyl tert-butyl ether by a Pseudomonas sp. strain grown on n-pentane

    Science.gov (United States)

    Li, S. S.; Wang, S.; Yan, W.

    2016-08-01

    When methyl tert-butyl ether (MTBE) is added as oxygenates it increases the octane number and decreases the release of nitric oxide from the incomplete combustion of reformulated gasoline. The extensive use of MTBE allowed it to be detectable as a pollutant in both ground-level and underground water worldwide. The present study focuses on the isolation and characterization of MTB-degrading microorganisms by cometabolism based on the results of growth on different carbon sources. It also focuses on the kinetic analysis and the continuous degradation of MTBE. A bacterial strain WL1 that can grow on both n-alkanes (C5-C8) and aromatics was isolated and named Pseudomonas sp. WL1 according to the 16S rDNA sequencing analysis. Strain WL1 could cometabolically degrade MTBE in the presence of n-alkanes with a desirable degradation rate. Diverse n-alkanes with different lengths of carbon chains showed significant influence on the degradation rate of MTBE and accumulation of tert-butyl alcohol (TBA). When strain WL1 cometabolically degraded MTBE in the presence of n-pentane, higher MTBE-degrading rate and lower TBA-accumulation were observed (Vmax = 38.1 nmol/min/mgprotei, Ks = 6.8 mmol/L). In the continuous degrading experiment, the removal efficiency of MTBE by Pseudomonas sp. WL1 did not show any obvious decrease after five subsequent additions.

  7. Photocatalytic degradating methyl orange in water phase by UV-irradiated CdS carried by carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new candidate for photocatalytic degradating organic dyes,CdS carried by car-bon nanotubes(CdS/CNTs) ,is reported. The degradation ratio curves of methyl orange in water phase show that the capability for degradating organic molecules of CdS/CNTs is obviously higher than that of separated CdS. The degradation ca-pability enhances as the increase of the amount of net CdS catalyst,the ratio of carbon nanotubes to CdS,and the area of the template,and is influenced by the pH value and the temperature of aqueous solution. These results suggest that the photocatalyst of CdS/CNTs is very suitable for potential applications in organic waste removal from water.

  8. Photocatalytic degradating methyl orange in water phase by UV-irradiated CdS carried by carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    LI ChenSha; TANG YaPing; KANG BoNan; WANG BinSong; ZHOU Feng; MA Qiang; XIAO Ji; WANG DaZhi; LIANG Ji

    2007-01-01

    A new candidate for photocatalytic degradating organic dyes, CdS carried by carbon nanotubes (CdS/CNTs), is reported. The degradation ratio curves of methyl orange in water phase show that the capability for degradating organic molecules of CdS/CNTs is obviously higher than that of separated CdS. The degradation capability enhances as the increase of the amount of net CdS catalyst, the ratio of carbon nanotubes to CdS, and the area of the template, and is influenced by the pH value and the temperature of aqueous solution. These results suggest that the photocatalyst of CdS/CNTs is very suitable for potential applications in organic waste removal from water.

  9. Photocatalytic degradation of methyl blue by silver ion-doped titania: Identification of degradation products by GC-MS and IC analysis.

    Science.gov (United States)

    Sahoo, Chittaranjan; Gupta, Ashok K

    2015-01-01

    An anionic triphenyl methane dye, methyl blue ((disodium;4-[4-[[4-(4-sulfonatoanilino)phenyl]-[4-(4-sulfonatophenyl)azaniumylidenecyclohexa-2,5-dien-1-ylidene]methyl]anilino]benzene sulfonate) was degraded photocatalytically with undoped micro-TiO2- and Ag(+)-doped micro TiO2 in a slurry-type batch reactor under UV irradiation and the efficiency was compared with that obtained using nano-TiO2- and Ag(+)-doped nano-TiO2. The influence of different parameters, i.e., photocatalyst loading, dye concentration, initial pH, temperature, depth of solution, interfering ions and electron acceptors on the dye degradation was investigated. The decolorization and mineralization efficiency was better for Ag(+)-doped micro-TiO2 than undoped micro-TiO2. Nano-TiO2 was more efficient than micro-TiO2, while Ag(+)-doped nano-TiO2 was the most efficient of all. Cost analysis showed degradation using micro-TiO2- and Ag(+)-doped micro-TiO2 are much cheaper than that using nano-TiO2 and Ag(+)-doped nano-TiO2. Therefore Ag(+)-doped micro-TiO2 was used for the detailed study. The degradation products formed were identified using GC-MS analysis after photocatalytic degradation for 180 min with Ag(+) -doped micro TiO2. Ion chromatography analysis was carried out for anions to identify the end products of degradation.

  10. Photocatalytic Degradation of Methyl Thionine Chloride in Aqueous Solution over Nanometer ( CdS/TiO2 )/MCM-41

    Institute of Scientific and Technical Information of China (English)

    XUE Hanling; LI Jianwei; GE Lingmei

    2006-01-01

    ( CdS / TiO2 )/MCM-41 loaded nanometer photocatalyst was prepared by the sol-gel method and dipping process, the photocatalytic degradation of methyl thionine chloride in water was investigated by using the photocatalyst. The experimental results show that the optimum concentration of CdS over TiO2 was 3% ( molar ratio ), the photocatalytic activity was enhanced when making TiO2 the anatase phase with a rise of the roasting temperature, and the carrier, mesoporous molecular sieve MCM- 41, was beneficial to improving the photocatalytic activity of TiO2 for photocatalytic degradation of methyl thionine chloride. The morphology and the crystalline phase of the photocatalyst were discussed by means of XRD and SEM techniques, and the reaction mechanism of catalytic properties was also discussed.

  11. Catalyzed oxidative degradation of methyl orange over Au catalyst prepared by ionic liquid-polymer modified silica

    Science.gov (United States)

    Wang, Y.; Guo, J. S.

    2015-07-01

    A new type of hybrid material was prepared by grafting an ionic liquid monomer, 1-(p-vinylbenzyl)-3-methylimidazolium chloride, on the surface of the porous silica which was synthesized via sodium silicate hydrolysis. The as-synthesized products were characterized by scanning electron microscope, nitrogen physisorption experiment, thermogravimetric analysis and Fourier transform infrared spectra. A catalyst with Au was prepared using the hybrid material as carrier. The experimental results show that the catalyst exhibits a better catalytic effect of hydrogen peroxide on the degradation of methyl orange. The reason may be that the metal component of the catalyst facilitated the dissociation of hydrogen peroxide to produce abundant highly active free radicals which can rapidly ruin the structure of methyl orange molecules in water. Finally, a probable catalytic degradation mechanism based on diffusion was discussed.

  12. In situ preparation of cubic Cu2O-RGO nanocomposites for enhanced visible-light degradation of methyl orange

    Science.gov (United States)

    Zhang, Wei; Li, Xiaolin; Yang, Zhi; Tang, Xuehui; Ma, Yujie; Li, Ming; Hu, Nantao; Wei, Hao; Zhang, Yafei

    2016-07-01

    There has been a growing interest in gathering together photocatalysis of semiconductors, like cuprous oxide (Cu2O), and the excellent electron transmittability of graphene to produce a graphene-based semiconductor for photocatalytic degradation. In this paper, a mild one-pot in situ synthesis of cubic cuprous oxide-reduced graphene oxide (Cu2O-RGO) nanocomposites has been proposed for the removal of methyl orange. In contrast to pure cubic Cu2O particles under similar preparation conditions, the cubic Cu2O-RGO nanocomposites demonstrate enhanced visible-light-driven photocatalytic activity for methyl orange dye with a 100% degradation rate in 100 min. The enhanced photocatalytic performance is mainly attributed to the increased charge transportation, effective separation of photoelectrons from vacancies, and the improved contact area.

  13. Enhanced ultrasound-assisted degradation of methyl orange and metronidazole by rectorite-supported nanoscale zero-valent iron.

    Science.gov (United States)

    Yuan, Na; Zhang, Gaoke; Guo, Sheng; Wan, Zhen

    2016-01-01

    In this study, the rectorite-supported nanoscale zero-valent iron (nZVI/R) was synthesized through a reduction method. X-ray diffraction analysis showed the existence of the nZVI in the nZVI/R composite and X-ray photoelectron spectroscopy analysis indicated that the nZVI particles were partly oxidized into iron oxide. Scanning electron microscopy analysis revealed that the nZVI particles were highly dispersed on the surface of the rectorite. The specific surface area of the nZVI/R composite is 21.43 m(2)/g, which was higher than that of rectorite (4.30 m(2)/g) and nZVI (17.97 m(2)/g). In the presence of ultrasound (US), the degradation of methyl orange and metronidazole by the nZVI/R composite was over 93% and 97% within 20 min, respectively, which is much higher than that by the rectorite and the nZVI. The degradation ratio of methyl orange and metronidazole by the nZVI/R composite under US was 1.7 and 1.8 times as high as that by the nZVI/R composite without US, respectively. The mechanism of the enhanced degradation of methyl orange and metronidazole under US irradiation was studied. These results indicate that the US/nZVI/R process has great potential application value for treatment of dye wastewater and medicine wastewater.

  14. Degradation of Triazine-2-(14C Metsulfuron-Methyl in Soil from an Oil Palm Plantation.

    Directory of Open Access Journals (Sweden)

    B S Ismail

    Full Text Available Triazine-2-(14C metsulfuron-methyl is a selective, systemic sulfonylurea herbicide. Degradation studies in soils are essential for the evaluation of the persistence of pesticides and their breakdown products. The purpose of the present study was to investigate the degradation of triazine-2-(14C metsulfuron-methyl in soil under laboratory conditions. A High Performance Liquid Chromatograph (HPLC equipped with an UV detector and an on-line radio-chemical detector, plus a Supelco Discovery column (250 x 4.6 mm, 5 μm, and PRP-1 column (305 x 7.0 mm, 10 μm was used for the HPLC analysis. The radioactivity was determined by a Liquid Scintillation Counter (LSC in scintillation fluid. The soil used was both sterilized and non-sterilized in order to observe the involvement of soil microbes. The estimated DT50 and DT90 values of metsulfuron-methyl in a non-sterile system were observed to be 13 and 44 days, whereas in sterilized soil, the DT50 and DT90 were 31 and 70 days, respectively. The principal degradation product after 60 days was CO2. The higher cumulative amount of (14CO2 in (14C-triazine in the non-sterilized soil compared to that in the sterile system suggests that biological degradation by soil micro-organisms significantly contributes to the dissipation of the compound. The major routes of degradation were O-demethylation, sulfonylurea bridge cleavage and the triazine "ring-opened."

  15. Degradation of Triazine-2-14C Metsulfuron–Methyl in Soil from an Oil Palm Plantation

    Science.gov (United States)

    B. S., Ismail

    2015-01-01

    Triazine-2-14C metsulfuron–methyl is a selective, systemic sulfonylurea herbicide. Degradation studies in soils are essential for the evaluation of the persistence of pesticides and their breakdown products. The purpose of the present study was to investigate the degradation of triazine-2-14C metsulfuron–methyl in soil under laboratory conditions. A High Performance Liquid Chromatograph (HPLC) equipped with an UV detector and an on-line radio-chemical detector, plus a Supelco Discovery column (250 x 4.6 mm, 5 μm), and PRP–1 column (305 x 7.0 mm, 10 μm) was used for the HPLC analysis. The radioactivity was determined by a Liquid Scintillation Counter (LSC) in scintillation fluid. The soil used was both sterilized and non-sterilized in order to observe the involvement of soil microbes. The estimated DT50 and DT90 values of metsulfuron-methyl in a non-sterile system were observed to be 13 and 44 days, whereas in sterilized soil, the DT50 and DT90 were 31 and 70 days, respectively. The principal degradation product after 60 days was CO2. The higher cumulative amount of 14CO2 in 14C- triazine in the non-sterilized soil compared to that in the sterile system suggests that biological degradation by soil micro-organisms significantly contributes to the dissipation of the compound. The major routes of degradation were O-demethylation, sulfonylurea bridge cleavage and the triazine “ring-opened.” PMID:26437264

  16. Photocatalytic degradation of methyl orange dye by pristine titanium dioxide, zinc oxide, and graphene oxide nanostructures and their composites under visible light irradiation

    National Research Council Canada - National Science Library

    Ramesh Raliya; Caroline Avery; Sampa Chakrabarti; Pratim Biswas

    2017-01-01

    .... Degradation of an azo dye, methyl orange (MO), was tested in simulated wastewater with different oxide nanomaterials acting as photocatalysts under visible light. Titanium dioxide (TiO2), zinc oxide (ZnO...

  17. Aerobic degradation of N-methyl-4-nitroaniline (MNA by Pseudomonas sp. strain FK357 isolated from soil.

    Directory of Open Access Journals (Sweden)

    Fazlurrahman Khan

    Full Text Available N-Methyl-4-nitroaniline (MNA is used as an additive to lower the melting temperature of energetic materials in the synthesis of insensitive explosives. Although the biotransformation of MNA under anaerobic condition has been reported, its aerobic microbial degradation has not been documented yet. A soil microcosms study showed the efficient aerobic degradation of MNA by the inhabitant soil microorganisms. An aerobic bacterium, Pseudomonas sp. strain FK357, able to utilize MNA as the sole carbon, nitrogen, and energy source, was isolated from soil microcosms. HPLC and GC-MS analysis of the samples obtained from growth and resting cell studies showed the formation of 4-nitroaniline (4-NA, 4-aminophenol (4-AP, and 1, 2, 4-benzenetriol (BT as major metabolic intermediates in the MNA degradation pathway. Enzymatic assay carried out on cell-free lysates of MNA grown cells confirmed N-demethylation reaction is the first step of MNA degradation with the formation of 4-NA and formaldehyde products. Flavin-dependent transformation of 4-NA to 4-AP in cell extracts demonstrated that the second step of MNA degradation is a monooxygenation. Furthermore, conversion of 4-AP to BT by MNA grown cells indicates the involvement of oxidative deamination (release of NH2 substituent reaction in third step of MNA degradation. Subsequent degradation of BT occurs by the action of benzenetriol 1, 2-dioxygenase as reported for the degradation of 4-nitrophenol. This is the first report on aerobic degradation of MNA by a single bacterium along with elucidation of metabolic pathway.

  18. Sonocatalytic degradation of methyl parathion in the presence of nanometer and ordinary anatase titanium dioxide catalysts and comparison of their sonocatalytic abilities.

    Science.gov (United States)

    Wang, Jun; Pan, Zhijun; Zhang, Zhaohong; Zhang, Xiangdong; Wen, Fuyu; Ma, Teng; Jiang, Yuefeng; Wang, Lei; Xu, Liang; Kang, Pingli

    2006-09-01

    The degradation of methyl parathion (O,O-dimethyl-O-(4-nitrophenyl)-phosphorothioate) using anatase titanium dioxide (TiO(2)) powder as heterogeneous sonocatalysts is reported. The influences of reaction parameters such as the species of TiO(2) sonocatalysts, methyl parathion concentrations, TiO(2) adding amount, pH, ultrasonic intensity, ultrasonic frequency and temperature have been investigated and the optimal conditions for eliminating methyl parathion have been identified. The efficiencies of sonocatalytic degradation in both nanometer and ordinary anatase systems are compared and the results indicate that the sonocatalytic activity of nanometer anatase TiO(2) powder is better than that of ordinary anatase TiO(2) powder. The primary degradation and the total mineralization of methyl parathion have been monitored by high performance liquid chromatography (HPLC) and UV-vis spectra, respectively. Methyl parathion got destroyed to some extent in both nanometer and ordinary anatase systems under ultrasonic irradiation. The kinetics for the degradation process of methyl parathion follows the first-order reaction. The degradation ratio of methyl parathion surpassed 90% within 50min in the optimal experiment conditions.

  19. Potassium channel antagonists 4-aminopyridine and the T-butyl carbamate derivative of 4-aminopyridine improve hind limb function in chronically non-ambulatory dogs; a blinded, placebo-controlled trial.

    Directory of Open Access Journals (Sweden)

    Ji-Hey Lim

    Full Text Available 4-Aminopyridine (4-AP blocks voltage gated potassium channels, restoring conduction to demyelinated axons and improving function in demyelinating conditions, but its use is associated with adverse effects and benefit in spinal cord injury is limited. Derivatives of 4-AP have been developed to improve clinical efficacy while reducing toxicity. We compared the therapeutic effects of orally administered 4-AP and its t-butyl carbamate derivative (t-butyl with placebo in dogs that had suffered an acute spinal cord injury that left them chronically paralyzed. Nineteen dogs were entered into the trial, conducted in two-week treatment blocks starting with placebo, followed by random assignment to 4-AP or t-butyl, a washout and then the opposite medication followed by placebo. Investigators and owners were blinded to treatment group. Primary outcome measures included open field gait score (OFS, and treadmill based stepping score and regularity index, with additional secondary measures also considered. Thirteen of 19 dogs completed the protocol. Two were euthanized due to unrelated heath problems, two developed side effects and two were unable to complete for unrelated reasons. Dogs showed significant improvement in supported stepping score (from 17.39 to 37.24% with 4-AP; 16.85 to 29.18% with t-butyl p<0.0001 and OFS (from 3.63 to 4.73 with 4-AP; 3.78 to 4.45 with t-butyl, p = 0.005. Response was individually variable and most dramatic in three dogs that were able to walk without support with treatment. No significant difference was found between 4-AP and t-butyl. No adverse effects were reported with t-butyl but gastrointestinal upset and seizures were observed in two dogs with 4-AP. In conclusion, both 4-AP and t-butyl significantly improved supported stepping ability in dogs with chronic spinal cord injury with no adverse effects noted with t-butyl. Drug response varied widely between individuals, highlighting the need to understand the factors

  20. Novel Oxidation of Cyclosporin A: Preparation of Cyclosporin Methyl Vinyl Ketone (Cs-MVK)

    Science.gov (United States)

    Cyclosporin A (CsA) was converted into cyclosporin methyl vinyl ketone (Cs-MVK) by either a biocatalytic method utilizing 1-hydroxybenzotriazole-mediated laccase oxidation or by a chemical oxidation using t-butyl hydroperoxide and potassium ­periodate as co-oxidants. Cs-MVK is a novel, versatile sy...

  1. Alternative natural dyes in water purification: Anthocyanin as TiO 2-sensitizer in methyl orange photo-degradation

    Science.gov (United States)

    Zyoud, Ahed; Zaatar, Nidal; Saadeddin, Iyad; Helal, Muath H.; Campet, Guy; Hakim, Moulki; Park, DaeHoon; Hilal, Hikmat S.

    2011-06-01

    Natural molecular dye, anthocyanin, is described here as safe sensitizer for TiO 2 particles in photo-degradation of organic contaminants in water. The dye is a promising replacement for the more costly and hazardous heavy metal based systems, such as CdS particles and Ru-compounds. TiO 2/anthocyanin effectively catalyzed the photo-degradation of methyl orange contaminant under solar simulator radiation. The new TiO 2/anthocyanin catalyst showed comparable efficiency to earlier systems, while avoiding their hazardous nature. When supported onto activated carbon (AC) particles, the resulting AC/TiO 2/anthocyanin system showed enhanced efficiency and ease of recovery from the catalytic reaction mixture. The natural dye molecules showed the tendency to degrade under photo-degradation conditions, just like earlier hazardous sensitizers. However, complete mineralization of anthocyanin occurred leaving no traces of organic species in solution. Sensitizer degradation caused deactivation of the supported catalyst on recovery. Such a shortcoming was overcome by re-treatment of the recovered catalysts with fresh dye. Effects of different reaction parameters on the catalyst efficiency were studied. A mechanism, similar to earlier CdS-sensitized catalyst systems, is proposed for the TiO 2/anthocyanin catalyst.

  2. Cerium dioxide as a new reactive sorbent for fast degradation of parathion methyl and some other organophosphates

    Institute of Scientific and Technical Information of China (English)

    Pavel Janos; Lubos Vrtoch; Pavel Kuran; Martin Kormunda; Vaclav Stengl; Tomas Matys Grygar; Marek Dosek; Martin Stastny; Jakub Ederer; Vera Pilarova

    2014-01-01

    Cerium dioxide was used for the first time as reactive sorbent for the degradation of the organophosphate pesticides para-thion methyl, chlorpyrifos, dichlofenthion, fenchlorphos, and prothiofos, as well as of some chemical warfare agents-nerve gases soman and O-ethyl S-[2-(diisopropylamino) ethyl] methylphosphonothioate (VX). CeO2 specimens were prepared by calcination of basic cerous carbonate obtained by precipitation from an aqueous solution. The CeO2 samples containing certain amounts (1 wt.%-5 wt.%) of the neighboring lanthanides (La, Pr, Nd) were prepared in a similar way from pure lanthanide salts. It was shown that ceria accelerated markedly the decomposition of parathion methyl causing the cleavage of the P-O-aryl bond in the pesticide molecule. A similar reaction mechanism was proposed for the degradation of other organophosphate pesticides and nerve agents. The degradation times (reaction half-times) were in an order of minutes in the presence of CeO2, compared to hours or days under common environ-mental conditions. The reaction in suitable organic solvents allowed conversions of about 90%for parathion methyl loading of 20 mg pesticide/g CeO2 within 2 h with a reactant half-life in the order of 0.1 min. The key parameter governing the degradation efficiency of CeO2 was the temperature during calcination. At optimum calcination temperature (about 773.15 K), the produced ceria retained a sufficiently high surface area, and attained an optimum degree of crystallinity (related to a number of crystal defects, and thus poten-tial reactive sites). The presence of other lanthanides somewhat decreased the reaction rate, but this effect was not detrimental and permitted the possible use of chemically impure ceria as a reactive sorbent. A fast organophosphate degradation was demonstrated not only in non-polar solvents (such as heptane), but also in polar aprotic solvents (acetonitrile, acetone) that are miscible with water. This opens new possibilities for

  3. Effect of reaction conditions on methyl red degradation mediated by boron and nitrogen doped TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Galenda, A., E-mail: galenda@ieni.cnr.it [CNR-IENI, Istituto per l’Energetica e le Interfasi, Corso Stati Uniti, 4 35127 Padova (Italy); Crociani, L.; Habra, N. El; Favaro, M. [CNR-IENI, Istituto per l’Energetica e le Interfasi, Corso Stati Uniti, 4 35127 Padova (Italy); Natile, M.M. [CNR-IENI, Istituto per l’Energetica e le Interfasi, Dipartimento di Scienze Chimiche, Università di Padova, via F. Marzolo, 1 35131 Padova (Italy); Rossetto, G. [CNR-IENI, Istituto per l’Energetica e le Interfasi, Corso Stati Uniti, 4 35127 Padova (Italy)

    2014-09-30

    Highlights: • Boron and/or nitrogen-doped TiO{sub 2} for photocatalytic wastewater treatment. • Methyl red degradation/mineralisation as a function of pH, acids and dopants. • Adsorption time influence on photocatalytic process. • Recovery of worn-out catalyst. - Abstract: Nowadays the employment of renewable and sustainable energy sources, and solar light as main option, becomes an urgent need. Photocatalytic processes received great attention in wastewater treatment due to their cheapness, environmental compatibility and optimal performances. Despite the general low selectivity of the photocatalysts, an accurate optimisation of the operational parameters needs to be carried out in order to maximise the process yield. Because of this reason, the present contribution aims to deepen either the knowledge in boron and/or nitrogen doped TiO{sub 2}-based systems and their employment in methyl red removal from aqueous solutions. The samples were obtained by coprecipitation and characterised by XRD, SEM, BET specific surface area, UV–vis and XPS techniques. The catalytic activity was for the first time carefully evaluated with respect to methyl red photodegradation in different conditions as a function of working pH, counter-ions and pre-adsorption time. An ad-hoc study was performed on the importance of the pre-adsorption of the dye, suggesting that an extended adsorption is useless for the catalyst photoactivity, while a partial coverage is preferable. The photocatalytic tests demonstrate the positive influence of boron doping in photo-activated reactions and the great importance of the operational parameters with respect to the simple methyl red bleaching rather than the overall pollutant mineralisation. It is proved, indeed, that different working pH, acidifying means and substrate pre-adsorption time can enhance or limit the catalyst performances with respect to the complete pollutant degradation rather than its partial breakage.

  4. Isolation and characterization of a novel 2-methyl-4-chlorophenoxyacetic acid-degrading Enterobacter sp. strain SE08.

    Science.gov (United States)

    Tan, Lin; Hu, Qiulong; Xiong, Xingyao; Su, Xiaojun; Huang, Yanning; Jiang, Ziwei; Zhou, Qingming; Zhao, Songyi; Zeng, Wei-ai

    2013-10-01

    A bacterial strain (SE08) capable of utilizing 2-methyl-4-chlorophenoxy acetic acid (MCPA) as the sole carbon and energy source for growth was isolated by continuous enrichment culturing in minimal salt medium (MSM) from a long term MCPA exposed soil. This bacterial strain was identified as Enterobacter sp. based on morphological, physiological and biochemical tests, as well as 16S rRNA sequence analysis. Its ability to degrade MCPA was determined using high performance liquid chromatography. The strain SE08 can tolerate unusually high MCPA concentrations (125-2000mg/L). The influences of culturing factors (initial concentration, pH, and temperature) on the bacterial growth and substrate degradation were studied. The results showed that the optimal MCPA degradation occurred at an MCPA concentration of 500mg/L, 30°C and pH 6.0. Under these conditions, 68.5 percent of MCPA in MSM was degraded by SE08, and the OD600nm reached 0.64 after culturing for 72h. The degradation of MCPA could be enhanced by addition of both carbon and nitrogen sources. At an initial MCPA concentration of 500mg/L, when 5g/L glucose and 2.5g/L yeast extract were added into the MSM media, the MCPA degradation was significantly increased to 83.8 percent, and OD600nm was increased to 1.09 after incubation at 30°C and pH 6.0 for 72h. This is the first study showing that an Enterobacter sp. strain is capable of degrading MCPA, which might provide a new approach for the remediation of MCPA contaminated soil and contribute to the limited knowledge about the function of Enterobacter species.

  5. Degradation of methyl and ethyl mercury into inorganic mercury by other reactive oxygen species besides hydroxyl radical

    Energy Technology Data Exchange (ETDEWEB)

    Suda, Ikuo; Takahashi, Hitoshi (Kumamoto Univ. Medical School (Japan). Inst. for Medical Immunology)

    1992-01-01

    Degradation of methyl mercury (MeHg) and ethyl Hg (EtHg) with reactive oxygens was studied in vitro by using peroxidase-hydrogen peroxide (H{sub 2}O{sub 2})-halide and rose bengal-ultraviolet light A systems. For this purpose, the direct determination method for inorganic Hg was employed. Both systems could effectively degrade EtHg, and MeHg to some extent. Degradation of MeHg and EtHg with the myeloperoxidase (MPO)-H{sub 2}O{sub 2}-chloride system was inhibited by MPO inhibitors (cyanide and azide), catalase, hypochlorous acid (HOCl) scavengers (glycine, alanine, serine and taurine), 1,4-diazabicyclo(2,2,2)octane and 2,5-dimethylfuran, but not by hydroxyl radical scavengers (ethanol and mannitol). Iodide was more effective than chloride as the halide component. Lactoperoxidase (LPO) could substitute for MPO in the iodide, but not the chloride system. With MPO-H{sub 2}O{sub 2}-chloride, MPO-H{sub 2}O{sub 2}-iodide and LPO-H{sub 2}O{sub 2}-iodide systems, we observed the increased degradation of EtHg in deuterium oxide (D{sub 2}O) medium better than that in H{sub 2}O medium. The D{sub 2}O effect upon MeHg degradation was extremely weak. These results suggested that HOCl (or HOI) might be also capable of degrading MeHg and EtHg, besides the hydroxyl radical already reported by us. Singlet oxygen could degrade EtHg but not MeHg. (orig.).

  6. Synthesis of TiO2 nano-particles and their photocatalytic activity for formaldehyde and methyl orange degradation

    Institute of Scientific and Technical Information of China (English)

    XIAO Xinyan; LIAO Dongliang; ZHANG Huiping; CHEN Huanqin

    2007-01-01

    TiO2 nano-particles were synthesized by sol-gel technique and characterized by X-ray diffractometer (XRD)and transmission electron microscope (TEM).Their photocatalytic activities for formaldehyde (FA) and methyl orange (MO) degradation were tested using degradation rate (η) as an evaluation index.Based on the orthogonal test results,the optimal condition for TiO2 preparation was obtained.Results showed that particle sizes were in the range of 10-40 nm,and that prepared TiO2 had better photocatalytic activity than P25.A simplified model was developed to evaluate the apparent quantum efficiency (Φapp) of this photocatalytic reaction system.

  7. Synthesis of allyl-glycidyl ether by the epoxidation of diallyl ether with t-butyl hydroperoxide over the Ti-MWW catalyst

    Directory of Open Access Journals (Sweden)

    Agnieszka Wróblewska

    2017-01-01

    Full Text Available In this paper, modified hydrothermal method for Ti-MWW catalyst preparation has been shown. Instrumental analysis of the zeolite material Ti-MWW has been performed by means of UV-vis spectrometry, infrared spectrometry (IR, scanning electron microscope (SEM, X-ray diffraction (XRD, and X-ray microanalysis. Moreover, the results of the epoxidation of diallyl ether (DAE over the titanium silicate catalyst Ti-MWW and in the presence of methanol have been presented. t-Butyl hydroperoxide have been applied for the first time as an oxidant for this process. The influence of temperature (20-130°C, DAE/TBHP molar ratio (1:1-3:1, methanol concentration (10-80 wt%, amount of catalyst (1-7 wt% and reaction time (60-1440 min. was studied. The main functions describing the process were determined on the basis of the results obtained from the gas chromatography method.

  8. Copolymerization of 1-hexene and 1-dodecene with 1,3-butadiene by a versatate/diisobutylaluminum hydride/t-butyl chloride catalyst system

    Directory of Open Access Journals (Sweden)

    Gustavo Monteiro da Silva

    2014-01-01

    Full Text Available The aim of this study was to incorporate an alpha-olefin (1-hexene or 1-dodecene in a high cis polybutadiene chain, using a neodymium versatate/diisobutylaluminum hydride/t-butyl chloride catalyst system. The influence of alpha-olefin on polymerization reaction and polymer characteristics, using different weight ratios of butadiene/α-olefin, was evaluated. The copolymers were characterized by SEC, FTIR, NMR, TGA and viscosimetric analysis. The thermal stability of the polymer tended to increase with incorporation of alpha-olefins, while its microstructure was not affected. The weight average molecular mass (Mw tended to increase and the polymerization conversion tended to decrease with increasing alpha-olefins content. The copolymers showed a lower intrinsic viscosity than for the homopolymer. The results indicated that the alpha-olefins were incorporated in the polybutadiene chain.

  9. Degradation of methyl orange using short-wavelength UV irradiation with oxygen microbubbles.

    Science.gov (United States)

    Tasaki, Tsutomu; Wada, Tsubasa; Fujimoto, Kanji; Kai, Shinji; Ohe, Kaoru; Oshima, Tatsuya; Baba, Yoshinari; Kukizaki, Masato

    2009-03-15

    A novel wastewater treatment technique using 8 W low-pressure mercury lamps in the presence of uniform-sized microbubbles (diameter = 5.79 microm) was investigated for the decomposition of methyl orange as a model compound in aqueous solution. Photodegradation experiments were conducted with a BLB black light blue lamp (365 nm), a UV-C germicidal lamp (254 nm) and an ozone lamp (185 nm+254 nm) both with and without oxygen microbubbles. The results show that the oxygen microbubbles accelerated the decolorization rate of methyl orange under 185+254 nm irradiation. In contrast, the microbubbles under 365 and 254 nm irradiation were unaffected on the decolorization of methyl orange. It was found that the pseudo-zero order decolorization reaction constant in microbubble system is 2.1 times higher than that in conventional large bubble system. Total organic carbon (TOC) reduction rate of methyl orange was greatly enhanced by oxygen microbubble under 185+254 nm irradiation, however, TOC reduction rate by nitrogen microbubble was much slower than that with 185+254 nm irradiation only. Possible reaction mechanisms for the decolorization and mineralization of methyl orange both with oxygen and nitrogen mirobubbles were proposed in this study.

  10. The efficient photocatalytic degradation of methyl tert-butyl ether under Pd/ZnO and visible light irradiation.

    Science.gov (United States)

    Seddigi, Zaki S; Ahmed, Saleh A; Bumajdad, Ali; Danish, Ekram Y; Shawky, Ahmed M; Gondal, Mohammed A; Soylak, Mustafa

    2015-01-01

    Methyl tert-butyl ether is a commonly used fuel oxygenate that is present in gasoline. It was introduced to eliminate the use of leaded gasoline and to improve the octane quality because it aids in the complete combustion of fuel by supplying oxygen during the combustion process. Over the past decade, the use of MTBE has increased tremendously worldwide. For obvious reasons relating to accidental spillage, MTBE started to appear as an environmental and human health threat because of its nonbiodegradable nature and carcinogenic potential, respectively. In this work, MTBE was degraded with the help of an advanced oxidation process through the use of zinc oxide as a photocatalyst in the presence of visible light. A mixture of 200 mg of zinc oxide in 350 mL of 50 ppm MTBE aqueous solution was irradiated with visible light for a given time. The complete degradation of MTBE was recorded, and approximately 99% photocatalytic degradation of 100 ppm MTBE solution was observed. Additionally, the photoactivity of 1% Pd-doped ZnO was tested under similar conditions to understand the effect of Pd doping on ZnO. Our results obtained under visible light irradiation are very promising, and they could be further explored for the degradation of several nondegradable environmental pollutants.

  11. Degradation of methyl and ethyl mercury by singlet oxygen generated from sea water exposed to sunlight or ultraviolet light.

    Science.gov (United States)

    Suda, I; Suda, M; Hirayama, K

    1993-01-01

    Photodegradation of methyl mercury (MeHg) and ethyl Hg (EtHg) in sea water was studied by sunlight or ultraviolet (UV) light exposure, and by determining inorganic Hg produced by degradation. Sea water containing 1 microM MeHg or EtHg was exposed to sunlight or UV light. N-Acetyl-L-cysteine was added to the solution for preventing Hg loss during the light exposure. MeHg and EtHg in sea water were degraded by sunlight (> 280 nm), UV light A (320-400 nm) and UV light B (280-320 nm), though the amounts of inorganic Hg produced from MeHg were 1/6th to 1/12th those from EtHg. Inorganic Hg production was greater with increasing concentration of sea water. Degradation of MeHg and EtHg by the UV light A exposure was inhibited by singlet oxygen (1O2) trappers such as NaN3, 1,4-diazabicyclo[2,2,2]octane, histidine, methionine and 2,5-dimethylfuran. On the other hand, inhibitors or scavengers of superoxide anion, hydrogen peroxide or hydroxyl radical did not inhibit the photodegradation of alkyl Hg. These results suggested that 1O2 generated from sea water exposed to sunlight, UV light A or UV light B was the reactive oxygen species mainly responsible for the degradation of MeHg and EtHg.

  12. The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRM.

    Science.gov (United States)

    Daugaard, Iben; Kjeldsen, Tina E; Hager, Henrik; Hansen, Lise Lotte; Wojdacz, Tomasz K

    2015-12-01

    Readily accessible formalin-fixed paraffin embedded (FFPE) tissues are a highly valuable source of genetic material for molecular analyses in both research and in vitro diagnostics but frequently genetic material in those samples is highly degraded. With locus-specific methylation changes being widely investigated for use as biomarkers in various aspects of clinical disease management, we aimed to evaluate to what extent standard laboratory procedures can approximate the quality of the DNA extracted from FFPE samples prior to methylation analyses. DNA quality in 107 FFPE non-small cell lung cancer (NSCLC) samples was evaluated using spectrophotometry and gel electrophoresis. Subsequently, the quality assessment results were correlated with the results of locus specific methylation assessment with methylation sensitive high resolution melting (MS-HRM). The correlation of template quality with PCR amplification performance and HRM based methylation detection indicated a significant influence of DNA quality on PCR amplification but not on methylation assessment. In conclusion, standard laboratory procedures fairly well approximate DNA degradation of FFPE samples and DNA degradation does not seem to considerably affect locus-specific methylation assessment by MS-HRM.

  13. Photo degradation of methyl orange an azo dye by advanced Fenton process using zero valent metallic iron: influence of various reaction parameters and its degradation mechanism.

    Science.gov (United States)

    Gomathi Devi, L; Girish Kumar, S; Mohan Reddy, K; Munikrishnappa, C

    2009-05-30

    Advanced Fenton process (AFP) using zero valent metallic iron (ZVMI) is studied as a potential technique to degrade the azo dye in the aqueous medium. The influence of various reaction parameters like effect of iron dosage, concentration of H(2)O(2)/ammonium per sulfate (APS), initial dye concentration, effect of pH and the influence of radical scavenger are studied and optimum conditions are reported. The degradation rate decreased at higher iron dosages and also at higher oxidant concentrations due to the surface precipitation which deactivates the iron surface. The rate constant for the processes Fe(0)/UV and Fe(0)/APS/UV is twice compared to their respective Fe(0)/dark and Fe(0)/APS/dark processes. The rate constant for Fe(0)/H(2)O(2)/UV process is four times higher than Fe(0)/H(2)O(2)/dark process. The increase in the efficiency of Fe(0)/UV process is attributed to the cleavage of stable iron complexes which produces Fe(2+) ions that participates in cyclic Fenton mechanism for the generation of hydroxyl radicals. The increase in the efficiency of Fe(0)/APS/UV or H(2)O(2) compared to dark process is due to continuous generation of hydroxyl radicals and also due to the frequent photo reduction of Fe(3+) ions to Fe(2+) ions. Though H(2)O(2) is a better oxidant than APS in all respects, but it is more susceptible to deactivation by hydroxyl radical scavengers. The decrease in the rate constant in the presence of hydroxyl radical scavenger is more for H(2)O(2) than APS. Iron powder retains its recycling efficiency better in the presence of H(2)O(2) than APS. The decrease in the degradation rate in the presence of APS as an oxidant is due to the fact that generation of free radicals on iron surface is slower compared to H(2)O(2). Also, the excess acidity provided by APS retards the degradation rate as excess H(+) ions acts as hydroxyl radical scavenger. The degradation of Methyl Orange (MO) using Fe(0) is an acid driven process shows higher efficiency at pH 3. The

  14. Protein Phosphatase Methyl-Esterase PME-1 Protects Protein Phosphatase 2A from Ubiquitin/Proteasome Degradation.

    Science.gov (United States)

    Yabe, Ryotaro; Miura, Akane; Usui, Tatsuya; Mudrak, Ingrid; Ogris, Egon; Ohama, Takashi; Sato, Koichi

    2015-01-01

    Protein phosphatase 2A (PP2A) is a conserved essential enzyme that is implicated as a tumor suppressor based on its central role in phosphorylation-dependent signaling pathways. Protein phosphatase methyl esterase (PME-1) catalyzes specifically the demethylation of the C-terminal Leu309 residue of PP2A catalytic subunit (PP2Ac). It has been shown that PME-1 affects the activity of PP2A by demethylating PP2Ac, but also by directly binding to the phosphatase active site, suggesting loss of PME-1 in cells would enhance PP2A activity. However, here we show that PME-1 knockout mouse embryonic fibroblasts (MEFs) exhibit lower PP2A activity than wild type MEFs. Loss of PME-1 enhanced poly-ubiquitination of PP2Ac and shortened the half-life of PP2Ac protein resulting in reduced PP2Ac levels. Chemical inhibition of PME-1 and rescue experiments with wild type and mutated PME-1 revealed methyl-esterase activity was necessary to maintain PP2Ac protein levels. Our data demonstrate that PME-1 methyl-esterase activity protects PP2Ac from ubiquitin/proteasome degradation.

  15. Photocatalytic Degradation of Methyl Orange over Metalloporphyrins Supported on TiO2 Degussa P25

    Directory of Open Access Journals (Sweden)

    Xing-Jiao Huang

    2012-01-01

    Full Text Available The photocatalytic activity of meso-tetraphenylporphyrins with different metal centers (Fe, Co, Mn and Cu adsorbed on TiO2 (Degussa P25 surface has been investigated by carrying out the photodegradation of methyl orange (MO under visible and ultraviolet light irradiation. The photocatalysts were characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, diffuse reflectance UV (DRS-UV-vis and infrared spectra. Copper porphyrin-sensitized TiO2 photocatalyst (CuP-TiO2 showed excellent activity for the photodegradation of MO whether under visible or ultraviolet light irradiation. Natural Bond Orbital (NBO charges analysis showed that methyl orange ion is adsorbed easier by CuP-TiO2 catalyst due to the increase of induced interactions.

  16. The different effects of oxygen and air DBD plasma byproducts on the degradation of methyl violet 5BN.

    Science.gov (United States)

    Chen, Guangliang; Zhou, Mingyan; Chen, Shihua; Chen, Wenxing

    2009-12-30

    Through a novel design of the dielectric barrier discharge (DBD) plasma plume used in fabric-fiber surface modification, its discharge byproducts mainly including downstream gases and ultraviolet light were used to treat the dye solution. The different influence of oxygen and air DBD plasmas on the degradation of methyl violet 5BN (MV-5BN), which is widely used in textile industry, was investigated in this paper. The results showed that the cooperation between ultraviolet light and active species generated by the DBD plasma can decolorize MV-5BN effectively, and the chromophore peaks attributed to the -NN- bonds in MV-5BN molecule disappeared entirely when the azo dye solutions were treated for 25 min by the air and oxygen DBD plasmas. The degradation reaction followed an exponential kinetics over time, and the peak of aromatic derivatives at 209 nm in UV-vis spectra increased nearly 2.7 times when the dye solution was treated for 30 min by air DBD plasma. However, the oxygen DBD plasma could deplete the aromatic derivatives entirely. It is found that the formation of O(3) and NO(x) in the downstream gases of air and oxygen plasmas may be responsible for the different effects on the azo dye degradation.

  17. Identification of dimethylamine monooxygenase in marine bacteria reveals a metabolic bottleneck in the methylated amine degradation pathway.

    Science.gov (United States)

    Lidbury, Ian; Mausz, Michaela A; Scanlan, David J; Chen, Yin

    2017-07-01

    Methylated amines (MAs) are ubiquitous in the marine environment and their subsequent flux into the atmosphere can result in the formation of aerosols and ultimately cloud condensation nuclei. Therefore, these compounds have a potentially important role in climate regulation. Using Ruegeria pomeroyi as a model, we identified the genes encoding dimethylamine (DMA) monooxygenase (dmmABC) and demonstrate that this enzyme degrades DMA to monomethylamine (MMA). Although only dmmABC are required for enzyme activity in recombinant Escherichia coli, we found that an additional gene, dmmD, was required for the growth of R. pomeroyi on MAs. The dmmDABC genes are absent from the genomes of multiple marine bacteria, including all representatives of the cosmopolitan SAR11 clade. Consequently, the abundance of dmmDABC in marine metagenomes was substantially lower than the genes required for other metabolic steps of the MA degradation pathway. Thus, there is a genetic and potential metabolic bottleneck in the marine MA degradation pathway. Our data provide an explanation for the observation that DMA-derived secondary organic aerosols (SOAs) are among the most abundant SOAs detected in fine marine particles over the North and Tropical Atlantic Ocean.

  18. Aerobic degradation of methyl tert-butyl ether by a Proteobacteria strain in a closed culture system

    Institute of Scientific and Technical Information of China (English)

    ZHONG Wei-hong; CHEN Jian-meng; LU Zheng; CHEN Dong-zhi; CHEN Xiao

    2007-01-01

    The contamination of methyl tert-butyl ether (MTBE) in underground waters has become a widely concerned problem all over the world. In this study, a novel closed culture system with oxygen supplied by H2O2 was introduced for MTBE aerobic biodegradation. After 7 d, almost all MTBE was degraded by a pure culture, a member of β-Proteobacteria named as PM1, in a closed system with oxygen supply, while only 40% MTBE was degraded in one without oxygen supply. Dissolved oxygen (DO) levels of the broth in closed systems respectively with and without H2O2 were about 5-6 and 4 mg/L. Higher DO may improve the activity of monooxygemase, which is the key enzyme of metabolic pathway from MTBE to tert-butyl alcohol and finally to CO2, and may result in the increase of the degrading activity of PM1 cell. The purge and trap GC-MS result of the broth in closed systems showed that tert-butyl alcohol,isopronol and acetone were the main intermediate products.

  19. Enhanced photocatalytic degradation of methyl orange by CdS quantum dots sensitized platelike WO3 photoelectrodes

    Institute of Scientific and Technical Information of China (English)

    文瑾; 刘灿军; 杜勇; 胡传跃; 田修营

    2015-01-01

    CdS quantum dots sensitized platelike WO3 photoelectrodes were successfully synthesized by a facile hydrothermal method and a modified chemical bath deposition (CBD) technique. To further improve the stability of the photoelectrodes in alkaline environment, the platelike WO3 films were treated with TiCl4 to form a nano-TiO2 buffer layer on the WO3 plate surface before loading CdS QDs. The resulting electrodes were characterized by using XRD, SEM, HR-TEM and UV-vis spectrum. The photocatalytic activity of the resulting electrodes was investigated by degradation of methyl orange (MO) in aqueous solution. The photoelectrochemical (PEC) property of the resulting electrodes was also characterized by the linear sweep voltammetry. The results of both the degradation of MO and photocurrent tests indicated that the as-prepared CdS QDs sensitized WO3 platelike photoelectrodes exhibit a significant improvement in photocatalytic degradation and PEC activity under visible light irradiation, compared with unsupported CdS QDs electrodes. Significantly, coating the WO3 plates with nano-TiO2 obviously facilitate the charge separation and retards the charge-pair recombination, and results in a highest activity for QDs CdS/TiO2/WO3photoelectrodes.

  20. Degradation of a recalcitrant xenobiotic compound: methyl tert-butyl ether (MTBE) metabolism by mycobacterium austroafricanum; Degradation d'un compose xenobiotique recalcitrant: metabolisme du methyl tert-butyl ether (MTBE) par mycobacterium austroafricanum IFP 2012

    Energy Technology Data Exchange (ETDEWEB)

    Francois, A.

    2002-11-01

    Methyl tert-butyl ether (MTBE) is introduced up to 15% (vol/vol) in gasoline in order to obtain a good octane number and to prevent carbon monoxide emissions. However, as a consequence of storage tanks leakage, MTBE became one of the major pollutants of aquifers because of its very low biodegradability. The present study aimed at investigating the biodegradation of MTBE by Mycobacterium austroafricanum IFP 2012. The MTBE metabolic pathway was partially elucidated owing to the identification of some intermediates (tert-butyl formate (TBF), tert-butyl alcohol (TBA), a-hydroxy-isobutyric acid and acetone) and some enzymatic activities (MTBE/TBA monooxygenase (non hemic and inducible), TBF esterase, 2-propanol: NDMA oxidoreductase and another monooxygenase involved in acetone degradation). The involvement of TBF and the requirement of cobalt could be explanations for the low natural attenuation of MTBE; whereas the methoxy group does not seem to be implicated. (author)

  1. 钛酸纳米管光催化降解甲基橙的研究%Study on Photocatalytic Degradation of Methyl Orange by Titanic Acid Nanotubes

    Institute of Scientific and Technical Information of China (English)

    孔德国; 张红美; 杨瑛; 罗华平

    2013-01-01

    在紫外灯照射下,以钛酸纳米管为催化剂对甲基橙溶液进行光催化降解.结果表明,甲基橙初始浓度、催化剂用量及光照时间均对甲基橙降解率有一定程度的影响,而pH则几乎无影响.在35 mL初始浓度为10 mg/L甲基橙溶液、30 mg催化剂、pH中性、紫外光照60 min条件下,甲基橙降解率达到99.6%.%Using titanic acid nanotubes as catalyst,methyl orange was degraded under UV radiation.The results indicated that the initial concentration of methyl orange,amount of catalyst and illuminative time had some effects on the degradation rate,while pH of the solution hadn't influence on the degradation of methyl orange.The optimal conditions was 30 mg catalyst that added into 35 mL,pH 7.0,10 mg/L methyl orange solution,UV radiation for 60 minutes,the degradation rate of methyl orange reached 99.6%.

  2. Study of photo catalytic degradation of an industrial dye Ujala Supreme and Methyl Orange using SnO2-rGO composites

    Science.gov (United States)

    Rambabu, P.; Srivastava, S. K.; Turpu, G. R.

    2016-05-01

    The photo degradation nature of Methyl Orange and Ujala Supreme dyes are studied using SnO2-rGO composites. Initially, the Graphene Oxide (GO) is prepared by modified Hummers method. Then SnO2-rGO composite is prepared solgel method by taking SnCl2 and GO as precursor materials. The obtained powders are annealed in N2 ambient for two hours in a quartz tube. The structure of the obtained powder composites shows high crystallinity from XRD measurements. The Raman studies also show the D and G bands for the GO. The degradation behaviour is studied for different times with the help of UV-Vis spectrometer. The absorbance graphs reveal that the Ujala Supreme dye is degraded much faster in presence of SnO2-rGO where as Methyl Orange has shown almost no effect on degradation in presence of SnO2-rGO composite.

  3. Improved production of raw starch degrading enzyme by Aspergillus oryzae F-30 using methyl glucoside sesqui-stearate.

    Science.gov (United States)

    Sun, Hai-Yan; Wang, Lu; Liu, Jian-Wen; Peng, Ming

    2009-10-01

    The effect of methyl glucoside sesqui-stearate (MGS) on the production of raw starch degrading enzyme (RSDE) by Aspergillus oryzae F-30 was studied in this paper. The activity of RSDE formed by Aspergillus oryzae F-30 was enhanced dramatically by the addition of MGS to the medium. As a result, with the addition of 1.5 g MGS in 1 L basal medium, RSDE activity and productivity were 107 U mL(-1) and 1.49 U mL(-1) h(-1), 4.3-fold and 7.1-fold greater than the values obtained in the basal medium, respectively. The effect of MGS on the synthesis of RSDE by Aspergillus oryzae F-30 was also studied on a molecular level. It was observed that the regulation of RSDE synthesis in Aspergillus oryzae F-30 occurs at both transcriptional and translational level and the enzyme synthesis was provoked by the addition of MGS at transcriptional level.

  4. Cube-like Cu2MoS4 photocatalysts for visible light-driven degradation of methyl orange

    Directory of Open Access Journals (Sweden)

    Ke Zhang

    2015-07-01

    Full Text Available Cube-like Cu2MoS4 nanoparticles with low-index facets and high crystallinity were fabricated via a hydrothermal method. The as-obtained nanocubes with an average size of 40-60 nm are composed of stacking-Cu2MoS4 layers separated by a weak Van der Waals gap of 0.5 nm. A strong absorption at visible light region is observed in the nanocube aqueous solution, indicating its optical-band gap of 1.78 eV. The photocatalytic measurements reveal that the nanocubes can thoroughly induce the degradation of methyl orange under visible light irradiation with good structural stability. Our finding may provide a way in design and fabrication of transition metal dichalcogenide nanostructures for practical applications.

  5. Degradation of Methyl Blue Using Fe-Tourmaline as a Novel Photocatalyst

    OpenAIRE

    Rong Ji; Jianqiu Chen; Xuesen Bian

    2013-01-01

    This study investigated the photocatalytic activity of tourmaline by itself. Under irradiation of a 13 W, 254 nm UV lamp, 50% of methyl blue disappeared in the presence of 130 mg·L−1 tourmaline. The reaction was inhibited by the addition of ethanol, Cl−, SO42− and Cu2+, and promoted a little by addition of 50 mg/L Mg2+, which supports the inference of involvement of •OH radicals. This is the first proposal of tourmaline as a single photocatalyst without the need to add any artificial chemical...

  6. Effect of reaction conditions on methyl red degradation mediated by boron and nitrogen doped TiO2

    Science.gov (United States)

    Galenda, A.; Crociani, L.; Habra, N. El; Favaro, M.; Natile, M. M.; Rossetto, G.

    2014-09-01

    Nowadays the employment of renewable and sustainable energy sources, and solar light as main option, becomes an urgent need. Photocatalytic processes received great attention in wastewater treatment due to their cheapness, environmental compatibility and optimal performances. Despite the general low selectivity of the photocatalysts, an accurate optimisation of the operational parameters needs to be carried out in order to maximise the process yield. Because of this reason, the present contribution aims to deepen either the knowledge in boron and/or nitrogen doped TiO2-based systems and their employment in methyl red removal from aqueous solutions. The samples were obtained by coprecipitation and characterised by XRD, SEM, BET specific surface area, UV-vis and XPS techniques. The catalytic activity was for the first time carefully evaluated with respect to methyl red photodegradation in different conditions as a function of working pH, counter-ions and pre-adsorption time. An ad-hoc study was performed on the importance of the pre-adsorption of the dye, suggesting that an extended adsorption is useless for the catalyst photoactivity, while a partial coverage is preferable. The photocatalytic tests demonstrate the positive influence of boron doping in photo-activated reactions and the great importance of the operational parameters with respect to the simple methyl red bleaching rather than the overall pollutant mineralisation. It is proved, indeed, that different working pH, acidifying means and substrate pre-adsorption time can enhance or limit the catalyst performances with respect to the complete pollutant degradation rather than its partial breakage.

  7. Adsorption of 2,6-di-t-butyl-p-hydroxytoluene (BHT) on gold nanoparticles: Assignment and interpretation of surface-enhanced Raman scattering

    Science.gov (United States)

    Sun, Ying-Ying; Xie, Yun-Fei; Wang, He-Ya; Qian, He; Yao, Wei-Rong

    2012-11-01

    2,6-Di-t-butyl-p-hydroxytoluene (BHT), a common antioxidant, has been implicated in oil foods and food packaging materials as a substance that could migrate into the food supply chain and cause suppression of human respiratory enzymes. In this study, BHT solutions in different solvents were measured by surface enhanced Raman spectroscopy (SERS) in combination with SERS-active substrates: gold colloidal nanoparticles. The limit of detection of BHT can reach the level of 10 μg/mL with SERS in methanol. The Raman peak at 766 cm-1 was used as the index of quantitative analysis and the correlation coefficient was 0.9761. These results demonstrated the applicability of utilizing SERS to detect low concentrations of BHT. By comparing the features of SERS peaks with the density functional theory (DFT)-calculated Raman spectrum, the adsorption behavior of BHT on the surface of gold nanoparticles was analyzed in detail and it was determined that the dominant contribution to the SERS signal in this case should be the electromagnetic enhancement mechanism. A charge-transfer mechanism also contributed to the SERS signal for BHT adsorbed on gold nanoparticles by the Phsbnd O(H) (Ph = phenyl) coalescent format.

  8. Electric response in the antiferroelectric crystal of 4,4‧-di-t-butyl-2,2‧-bipyridyl with chloranilic acid

    Science.gov (United States)

    Rok, M.; Piecha-Bisiorek, A.; Szklarz, P.; Bator, G.; Sobczyk, L.

    2015-05-01

    The electric response was analyzed in the vicinity of the structural phase transition at 412 K in the single crystals of 2,5-dichloro-3,6-dihydroxy-p-benzoquinone (chloranilic acid, CLA) with 4,4‧-di-t-butyl-2,2‧-bipyridyl (dtBBP). The dielectric permittivity of the complex measured along the b direction between 300 and 440 K and at frequencies ranging from 500 Hz to 2 MHz indicates two phenomena. At low frequencies, dielectric losses are ascribed to the electric conductivity of the crystal, while at high frequencies, to the dielectric relaxation described by means of the Cole-Cole relationship. The parameters of the dielectric response: the relaxation time, τ, the dielectric increment, εο - ε∞, and the distribution parameter of the relaxation time, α, were estimated and analyzed. The low-temperature structure of the crystals indicates the antiferroelectric arrangement of the supramolecular hydrogen bonds. The dielectric results also presented for the deuterated crystals of dtBBP·CLA proved that the dynamics of protons in the hydrogen bonds are responsible for the mechanism of phase transition.

  9. Mechanism of Hydrotropic Action of Hydrotrope Sodium Cumene Sulfonate on the Solubility of Di-t-Butyl-Methane: A Molecular Dynamics Simulation Study.

    Science.gov (United States)

    Das, Shubhadip; Paul, Sandip

    2016-01-14

    Hydrotropes are special class of amphiphilic molecules that have an ability to solubilize the insoluble or sparingly soluble molecules in water. To find out the mechanism of hydrotropic action of hydrotropes on hydrophobic molecules, we have carried out classical molecular dynamics simulation of hydrophobic solute di-t-butyl-methane (DTBM) and hydrotrope sodium cumene sulfonate (SCS) in water with a regime of SCS concentrations. Our study demonstrates that, above the minimum hydrotrope concentration (MHC), the self-aggregation of SCS starts, and it creates a micellar-like environment in which the hydrophobic tail part of SCS points inward while its hydrophilic sulfonate group points outward to make favorable contact with water molecules. The formation of the hydrophobic core of SCS cluster creates a hydrophobic environment where the hydrophobic DTBM molecules are encapsulated. Interestingly, the determination of average water-SCS hydrogen bonds further suggests that the aggregate formation of SCS molecules has a negligible influence on it. Moreover, the calculations of Flory-Huggins interaction parameters also reveal favorable interactions between hydrotrope SCS and solute DTBM molecules. The implications of these findings on the mechanism of hydrotrope assisted enhanced solubility of hydrophobic molecules are discussed.

  10. Degradation of methyl and ethyl mercury into inorganic mercury by hydroxyl radical produced from rat liver microsomes

    Energy Technology Data Exchange (ETDEWEB)

    Suda, Ikuo (Kumamoto Univ. (Japan). Dept. of Pharmacology); Hirayama, Kimiko (Kumamoto Univ. (Japan). Coll. of Medical Science)

    1992-07-01

    Liver microsomes were prepared from Wistar rat by the Ca{sup 2+} aggregation method. Under various conditions, ethyl mercury chloride (EtHgCl) or methyl mercury chloride (MeHgCl) was incubated with the microsomal preparations. After the incubation, the amounts of inorganic Hg and hydroxyl radical (.OH) in the preparations were determined. Although the preparations alone produced a small amount of inorganic Hg and .OH, the addition of NADPH to the preparations increased both inorganic Hg and .OH production, which were further accelerated by the addition of KCN. The addition of Fe(III)EDTA, a .OH formation promoter, to the microsome-NADPH-KCN system increased inorganic Hg production, whereas the addition of diethylenetriamine pentaacetic acid, a .OH formation inhibitor, decreased inorganic Hg production. When .OH scavengers such as mannitol and dimethyl sulfoxide were added to this system, the inorganic Hg production decreased. These results suggested that the .OH produced from liver microsomes was responsible for the degradation of MeHg and EtHg. Since both .OH and inorganic Hg production decreased with a concomitant decrease in NADPH-cytochrome P-450 reductase activities, it is suggested that this enzyme may be involved in the microsomal degradation of MeHg and EtHg. (orig.).

  11. Hydrothermal Synthesis of CdIn2S4 and Photocatalytic Degradation of Methyl Orange under Visible-light Irradiation

    Institute of Scientific and Technical Information of China (English)

    CHEN Zhi-Xin; REN Zhu-Yun; XU Jing-Jing; XIAO Guang-Can; HE Yun-Hui

    2012-01-01

    CdIn2S4 microspheres were synthesized by a facile hydrothermal method with the temperature ranging from 120 to 200 ℃. X-ray diffraction, UV-vis diffuse reflectance spectroscopy, nitrogen sorption analysis, X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy were used to characterize the products. It was found that the crystallographic structure and optical property of the products synthesized at different temperature were almost the same. The SBEX of CdIn2S4 products decreased when the synthesized temperature increased, and the largest SBET was 33.16 m2 g-1 (120 ℃ sample). The degradation of methyl orange (MO) under the visible-light irradiation had been used as a probe reaction to investigate the photocatalytic activity of the as-prepared CdIn2S4, which showed that the CdIn2S4 sample synthesized at 120 ℃ presented the best photocatalytic activity for MO degradation.

  12. Degradation of methyl blue using Fe-tourmaline as a novel photocatalyst.

    Science.gov (United States)

    Bian, Xuesen; Chen, Jianqiu; Ji, Rong

    2013-01-24

    This study investigated the photocatalytic activity of tourmaline by itself. Under irradiation of a 13 W, 254 nm UV lamp, 50% of methyl blue disappeared in the presence of 130 mg·L⁻¹ tourmaline. The reaction was inhibited by the addition of ethanol, Cl⁻, SO₄²⁻ and Cu²⁺, and promoted a little by addition of 50 mg/L Mg²⁺, which supports the inference of involvement of •OH radicals. This is the first proposal of tourmaline as a single photocatalyst without the need to add any artificial chemical products. Results from this study might contribute to the broadened usage of this mineral to approach the goals of saving energy and eliminate direct or indirect environmental pollution.

  13. Degradation of Methyl Blue Using Fe-Tourmaline as a Novel Photocatalyst

    Directory of Open Access Journals (Sweden)

    Rong Ji

    2013-01-01

    Full Text Available This study investigated the photocatalytic activity of tourmaline by itself. Under irradiation of a 13 W, 254 nm UV lamp, 50% of methyl blue disappeared in the presence of 130 mg·L−1 tourmaline. The reaction was inhibited by the addition of ethanol, Cl−, SO42− and Cu2+, and promoted a little by addition of 50 mg/L Mg2+, which supports the inference of involvement of •OH radicals. This is the first proposal of tourmaline as a single photocatalyst without the need to add any artificial chemical products. Results from this study might contribute to the broadened usage of this mineral to approach the goals of saving energy and eliminate direct or indirect environmental pollution.

  14. Microbial degradation and fate in the environment of methyl tert-butyl ether and related fuel oxygenates.

    Science.gov (United States)

    Fayolle, F; Vandecasteele, J P; Monot, F

    2001-08-01

    Oxygenates, mainly methyl tert-butyl ether (MTBE), are commonly added to gasoline to enhance octane index and improve combustion efficiency. Other oxygenates used as gasoline additives are ethers such as ethyl tert-butyl ether (ETBE), tert-amyl methyl ether (TAME), and alcohols such as tert-butyl alcohol (TBA). As a result of its wide use, MTBE has been detected, mainly in the USA, in groundwater and surface waters, and is a cause of concern because of its possible health effects and other undesirable consequences. MTBE is a water-soluble and mobile compound that generates long pollution plumes in aquifers impacted by gasoline releases from leaking tanks. Field observations concur in estimating that, because of recalcitrance to biodegradation, natural attenuation is slow (half-life of at least 2 years). However, quite significant advances have been made in recent years concerning the microbiology of the degradation of MTBE and other oxygenated gasoline additives. The recalcitrance of these compounds results from the presence in their structure of an ether bond and of a tertiary carbon structure. For the most part, only aerobic microbial degradation systems have been reported so far. Consortia capable of mineralizing MTBE have been selected. Multiple instances of the cometabolism of MTBE with pure strains or with microflorae, growing on n-alkanes, isoalkanes, cyclohexane or ethers (diethyl ether, ETBE), have been described. MTBE was converted into TBA in all cases and was sometimes further degraded, but it was not used as a carbon source by the pure strains. However, mineralization of MTBE and TBA by several pure bacterial strains using these compounds as sole carbon and energy source has recently been reported. The pathways of metabolism of MTBE involve the initial attack by a monooxygenase. In several cases, the enzyme was characterized as a cytochrome P-450. After oxygenation, the release of a C -unit as formaldehyde or formate leads to the production of TBA

  15. Formic acid enhanced effective degradation of methyl orange dye in aqueous solutions under UV-Vis irradiation.

    Science.gov (United States)

    Wang, Jingjing; Bai, Renbi

    2016-09-15

    Developing efficient technologies to treat recalcitrant organic dye wastewater has long been of great research and practical interest. In this study, a small molecule, formic acid (FA), was applied as a process enhancer for the degradation of methyl orange (MO) dye as a model recalcitrant organic pollutant in aqueous solutions under the condition of UV-Vis light irradiation and air aeration at the ambient temperature of 25 °C. It was found that the decolouration of the dye solutions can be rapidly achieved, reducing the time, for example, from around 17.6 h without FA to mostly about less than 2 h with the presence of FA. The mineralization rate of MO dye reached as high as 81.8% in 1.5 h in the case of initial MO dye concentration at 25 mg L(-1), which is in contrast to nearly no mineralization of the MO dye for a similar system without the FA added. The study revealed that the generation of the H2O2 species in the system was enhanced and the produced OH radicals effectively contributed to the degradation of the MO dye. Process parameters such as the initial concentration of MO dye, FA dosage and solution pH were all found to have some effect on the degradation efficiency under the same condition of UV-Vis light irradiation and air aeration. The MO dye degradation performance was found to follow a first-order reaction rate to the MO dye concentration in most cases and there existed a positive correlation between the reaction rate constant and the initial FA concentration. Compared to the traditional H2O2/UV-Vis oxidation system, the use of FA as a process-enhancing agent can have the advantages of low cost, easy availability, and safe to use. The study hence demonstrates a promising approach to use a readily available small molecule of FA to enhance the degradation of recalcitrant organic pollutants, such as MO dye, especially for their pre-treatment.

  16. Fatty acid methyl esters yield and phorbol esters degradation during transesterification of Jatropha curcas oil by alkaline, acid and enzyme catalyzed method

    Directory of Open Access Journals (Sweden)

    Tosa Koji

    2017-01-01

    Full Text Available Jatropha curcas has recently been the focus of intense research as a raw material of biomass fuel. However, the carcinogenesis promoter action of the phorbol esters in the Jatropha raises concerns for health and environmental risk. The purpose of the present study is to determine the relationship between the fatty acid methyl esters yield and the phorbol esters degradation ratio during the transesterification of the Jatropha oil by alkaline, acid and enzyme catalyzed method, respectively. The phorbol esters in Jatropha oil were degraded during the transesterification of the Jatropha curcas oil by alkaline and acid catalyzed methanol methods. The degradation ratio was significantly correlated with the fatty acid methyl esters yields in alkaline catalyzed transesterification. The results obtained in this study suggest that the health and environmental risk of the phorbol esters in a Jatropha BDF can be significantly reduced by a complete transesterification of the crude oil by controlling the transesterification condition appropriately.

  17. Assessment of microbial populations in methyl ethyl ketone degrading biofilters by denaturing gradient gel electrophoresis.

    Science.gov (United States)

    Li, C; Moe, W M

    2004-05-01

    Denaturing gradient gel electrophoresis (DGGE) analysis of polymerase chain reaction-amplified genes coding for 16S rRNA was used to assess differences in bacterial community structure as a function of spatial location along the height of two biofilters used to treat a model waste gas stream containing methyl ethyl ketone (MEK). One of the laboratory-scale biofilters was operated as a conventional continuous-flow biofilter (CFB) and the other was operated as a sequencing batch biofilter (SBB). Both biofilters, inoculated with an identical starting culture and operated over a period lasting more than 300 days, received the same influent MEK concentration and same mass of MEK on a daily basis. The systems differed, however, in terms of the fraction of time during which contaminated air was supplied and the overall operating strategy employed. DGGE analysis indicated that microbial community structures differed as a function of height in each of the biofilters. The DGGE banding patterns also differed between the two biofilters, suggesting that operating strategies imposed on the biofilters imparted a sufficiently large selective pressure to influence microbial community structures. This may explain, in part, the superior performance of the SBB over the CFB during model transient loading conditions, and it may open new possibilities for purposely manipulating the microbial populations in biofilters treating gas-phase contaminants in a manner that leads to more favorable treatment performance.

  18. Preparation, Characterization and Photocatalytic Activities of TiO2 towards Methyl Red Degradation

    Directory of Open Access Journals (Sweden)

    Aware Dinkar Vishwanath

    2017-02-01

    Full Text Available Highly efficient, photoactive, nanocrystalline TiO2 powder was prepared with the help of modified sol-gel method. The prepared nanomaterials were characterized by modern techniques such as, TG-DTA, XRD, FE-SEM, EDX, TEM, BET surface area and FT-IR analysis for the identification of phase structure, phase composition and morphology. Formation of thermally stable, nanocrystalline, highley photocatalytic active, tetragonal anatase Titania was confirmed by TGA-DTA, XRD and HR-TEM. Similarly, FE-SEM confirms spherical, cauliflower like morphology for all Titania samples prepared with different cationic surfactants. The presence of mesoporous Titania was also confirmed by N2 adsorption-desorption. The effect of addition of various surfactants significantly improves the photocatalytic activity. Prepared nanomaterials were successfully tested under UV-Vis light region for photodegradation of Methyl Red (MR dye material which is act as water pollutant. The C16TAB assisted Titania exhibits enhance photocatalytic efficiency as compared to industrially applied photocatalyst, Titania (Degussa P25 and zinc oxide under similar experimental condition.

  19. Enhanced Photocatalytic Activity for Degradation of Methyl Orange over Silica-Titania

    Directory of Open Access Journals (Sweden)

    Yaping Guo

    2011-01-01

    Full Text Available Silica-modified titania (SMT powders with different atomic ratios of silica to titanium (Rx were successfully synthesized by a simple ultrasonic irradiation technique. The prepared samples were characterized by X-ray diffraction (XRD, FT-IR spectroscopy, transmission electron microscopy (TEM, X-ray photoelectron spectroscopy (XPS, and ultraviolet visible spectroscopy. The specific surface area was measured according to BET theory. Results indicate that the addition of silica to titania can suppress the crystalline size growth and the transformation of anatase phase to rutile phase of titania, enlarge specific surface area of the titania particles, and result in a blue shift of absorption edge compared to pure titania. The photocatalytic activity of the SMT samples was evaluated by decolorizing methyl orange aqueous solutions under UV-visible light irradiation. It was found in our study that this activity was affected by silica content, calcination temperature, H2SO4, and oxidants such as KIO4, (NH42S2O8 and H2O2. The results reveal that the photocatalytic activity of 0.1-SMT catalyst is the best among all samples calcined at 550°C for 1 h and it is 1.56 times higher than that of Degussa P-25 titania, which is a widely used commercial TiO2 made by Germany Degussa company and has been most widely used in industry as photocatalyst, antiultraviolet product, and thermal stabilizer. The optimal calcination temperature for preparation was 550°C. The photocatalytic activity of SMT samples is significantly enhanced by H2SO4 solution treatment and oxidants.

  20. Cigarette smoke induces proteasomal-mediated degradation of DNA methyltransferases and methyl CpG-/CpG domain-binding proteins in embryonic orofacial cells.

    Science.gov (United States)

    Mukhopadhyay, Partha; Greene, Robert M; Pisano, M Michele

    2015-12-01

    Orofacial clefts, the most prevalent of developmental anomalies, occur with a frequency of 1 in 700 live births. Maternal cigarette smoking during pregnancy represents a risk factor for having a child with a cleft lip and/or cleft palate. Using primary cultures of first branchial arch-derived cells (1-BA cells), which contribute to the formation of the lip and palate, the present study addressed the hypothesis that components of cigarette smoke alter global DNA methylation, and/or expression of DNA methyltransferases (Dnmts) and various methyl CpG-binding proteins. Primary cultures of 1-BA cells, exposed to 80μg/mL cigarette smoke extract (CSE) for 24h, exhibited a >13% decline in global DNA methylation and triggered proteasomal-mediated degradation of Dnmts (DNMT-1 and -3a), methyl CpG binding protein 2 (MeCP2) and methyl-CpG binding domain protein 3 (MBD-3). Pretreatment of 1-BA cells with the proteasomal inhibitor MG-132 completely reversed such degradation. Collectively, these data allow the suggestion of a potential epigenetic mechanism underlying maternal cigarette smoke exposure-induced orofacial clefting. Copyright © 2015 Elsevier Inc. All rights reserved.

  1. Electric response in the antiferroelectric crystal of 4,4′-di-t-butyl-2,2′-bipyridyl with chloranilic acid

    Energy Technology Data Exchange (ETDEWEB)

    Rok, M., E-mail: magdalena.rok@chem.uni.wroc.pl; Piecha-Bisiorek, A.; Szklarz, P.; Bator, G.; Sobczyk, L.

    2015-05-01

    Highlights: • The semiconducting properties of the crystals were disclosed in the organic complex. • Dielectric relaxation and dc conductivity were investigated. • Activation energy for the thermally activated processes of the σ{sub dc} was estimated. • The effect of hydrogen bonds on the mechanism of the phase transition and the electric properties of the crystal was discussed. - Abstract: The electric response was analyzed in the vicinity of the structural phase transition at 412 K in the single crystals of 2,5-dichloro-3,6-dihydroxy-p-benzoquinone (chloranilic acid, CLA) with 4,4′-di-t-butyl-2,2′-bipyridyl (dtBBP). The dielectric permittivity of the complex measured along the b direction between 300 and 440 K and at frequencies ranging from 500 Hz to 2 MHz indicates two phenomena. At low frequencies, dielectric losses are ascribed to the electric conductivity of the crystal, while at high frequencies, to the dielectric relaxation described by means of the Cole–Cole relationship. The parameters of the dielectric response: the relaxation time, τ, the dielectric increment, ε{sub ο} − ε{sub ∞}, and the distribution parameter of the relaxation time, α, were estimated and analyzed. The low-temperature structure of the crystals indicates the antiferroelectric arrangement of the supramolecular hydrogen bonds. The dielectric results also presented for the deuterated crystals of dtBBP·CLA proved that the dynamics of protons in the hydrogen bonds are responsible for the mechanism of phase transition.

  2. Electroanalytical studies on cadmium(II) selective potentiometric sensors based on t-butyl thiacalix[4]arene and thiacalix[4]arene in poly(vinyl chloride)

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Vinod K. [Department of Chemistry, Indian Institute of Technology, Roorkee 247667, Uttaranchal (India)], E-mail: vinodfcy@iitr.ernet.in; Jain, Ajay K. [Department of Chemistry, Indian Institute of Technology, Roorkee 247667, Uttaranchal (India); Ludwig, Rainer [Institute for Inorganic and Analytical Chemistry, Freie Universitaet, Berlin 14195 (Germany); Maheshwari, Gaurav [Department of Chemistry, Indian Institute of Technology, Roorkee 247667, Uttaranchal (India)

    2008-01-01

    Cd{sup 2+}-selective sensors have been fabricated from poly(vinyl chloride) (PVC) matrix membranes containing t-butyl thiacalix[4]arene (I) and thiacalix[4]arene (II) as electroactive materials. The addition of sodium tetraphenylborate and the plasticizer 2-nitrophenyl octyl ether has been found to improve the performance of the sensors substantially. The membranes of various compositions of the two thiacalixarenes have been investigated and it was found that the best performance was obtained for the membrane of composition II:PVC:NaTPB:NPOE in the ratio 5:120:3:150. The sensor shows a linear potential response for Cd{sup 2+} over a wide activity range 3.2 x 10{sup -6} to 1.0 x 10{sup -1} M with Nernstian compliance (29.5 mV decade{sup -1} of activity) in pH range 4.5-6.5 and a fast response time of {approx}8 s. The potentiometric selectivity coefficient values determined by matched potential method indicate excellent selectivity for Cd{sup 2+} ions over mono-, di- and trivalent interfering cations. The sensor exhibits adequate shelf life ({approx}3 months) with good reproducibility (S.D. {+-}0.2 mV) and can also be used in partially non-aqueous media having up to 20% (v/v) methanol, ethanol or acetone content with no significant change in the value of slope or working activity range. The sensor has been used in the potentiometric titration of Cd{sup 2+} with EDTA. The sensor could be successfully used for the quantification of cadmium in river water samples.

  3. Fabrication of TiO2/MoS2@zeolite photocatalyst and its photocatalytic activity for degradation of methyl orange under visible light

    Science.gov (United States)

    Zhang, Weiping; Xiao, Xinyan; Zheng, Lili; Wan, Caixia

    2015-12-01

    TiO2/MoS2@zeolite composite photocatalysts with visible-light activity were fabricated via a simple ultrasonic-hydrothermal synthesis method, using TiCl4 as Ti source, MoS2 as a direct sensitizer, glycerol water solution with certain dispersion agent as hydrolytic agent, and zeolite as carrier. The structure, morphology, composition, optical properties, and specific surface area of the as-prepared photocatalysts were characterized by using XRD, FTIR, SEM-EDS, TEM, XPS, UV-vis, PL and BET analyzer, respectively. And the photocatalytic degradation of methyl orange (MO) in aqueous suspension has been employed to evaluate the photocatalytic activity and degradation kinetics of as-prepared photocatalysts with xenon lamp as irradiation source. The results indicate that: (1) TiO2/MoS2@zeolite composite photocatalysts exhibit enhanced photocatalytic activities for methyl orange (MO) degradation compared to Degussa P25; (2) photocatalytic degradation of MO obeys Langmuir-Hinshelwood kinetic model (pseudo-first order reaction), and its degradation rate constant (kapp) (2.304 h-1) is higher than that of Degussa P25 (0.768 h-1); (3) the heterostructure consisted of zeolite, MoS2 and TiO2 nanostructure could provide synergistic effect for degradation of MO due to the efficient electron transfer process and better absorption property of TiO2/MoS2@zeolite composite photocatalyst.

  4. ZrO2/MoS2 heterojunction photocatalysts for efficient photocatalytic degradation of methyl orange

    Science.gov (United States)

    Prabhakar Vattikuti, Surya Veerendra; Byon, Chan; Reddy, Chandragiri Venkata

    2016-10-01

    We report a simple solution-chemistry approach for the synthesis of ZrO2/MoS2 hybrid photocatalysts, which contain MoS2 as a cocatalyst. The material is usually obtained by a wet chemical method using ZrO(NO3)2 or (NH4)6Mo7O24·4H2O and C8H6S as precursors. The structural features of obtained materials were characterized by X-ray diffraction (XRD), highresolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), thermal analysis (TG-DTA), N2 adsorption-desorption, and photoluminescence (PL). The influence on the photocatalytic activity of the MoS2 cocatalyst concentration with ZrO2 nanoparticles was studied. The MZr-2 hybrid sample had the highest photocatalytic activity for the degradation of methyl orange (MO), which was 8.45 times higher than that of pristine ZrO2 ascribed to high specific surface area and absorbance efficiency. Recycling experiments revealed that the reusability of the MZr-2 hybrid was due to the low photocorrosive effect and good catalytic stability. PL spectra confirmed the electronic interaction between ZrO2 and MoS2. The photoinduced electrons could be easily transferred from CB of ZrO2 to the MoS2 cocatalyst, which facilitate effective charge separation and enhanced the photocatalytic degradation in the UV region. A photocatalytic mechanism is proposed. It is believed that the ZrO2/MoS2 hybrid structure has promise as a photocatalyst with low cost and high efficiency for photoreactions.

  5. Enhanced visible light photocatalytic activity of copper-doped titanium oxide-zinc oxide heterojunction for methyl orange degradation

    Science.gov (United States)

    Dorraj, Masoumeh; Alizadeh, Mahdi; Sairi, Nor Asrina; Basirun, Wan Jefrey; Goh, Boon Tong; Woi, Pei Meng; Alias, Yatimah

    2017-08-01

    A novel Cu-doped TiO2 coupled with ZnO nanoparticles (Cu-TiO2/ZnO) was prepared by sol-gel method and subsequent precipitation for methyl orange (MO) photodegradation under visible light irradiation. The compositions and shapes of the as-prepared Cu-TiO2/ZnO nanocomposites were characterized by photoluminescence spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, UV-vis diffuse reflectance spectra and Brunauer-Emmett-Teller adsorption isotherm techniques. The Cu-TiO2/ZnO nanocomposites showed considerably higher photocatalytic activity for MO removal from water under visible light irradiation than that of single-doped semiconductors. The effects of Cu-TiO2 and ZnO mass ratios on the photocatalytic reaction were also studied. A coupling percentage of 30% ZnO exhibited the highest photocatalytic activity. The enhanced photocatalytic activity of the Cu-TiO2/ZnO nanocomposites was mainly attributed to heterojunction formation, which allowed the efficient separation of photoinduced electron-hole pairs at the interface. Moreover, these novel nanocomposites could be recycled during MO degradation in a three-cycle experiment without evident deactivation, which is particularly important in environmental applications.

  6. Mercury Isotope Constraints on Depth of Methylation and Degree of Photo-Degradation of Methylmercury in the Central Pacific Ocean

    Science.gov (United States)

    Blum, J. D.; Popp, B. N.; Johnson, M. W.; Drazen, J. C.; Choy, C. A.

    2012-12-01

    with a 50% mixture of MMHg produced at depth with MMHg that was photo-degraded at the surface. This may explain, in part, the much lower total Hg concentration in near-surface fish feeding at the same trophic position as deeper feeding fish. The ratio of Δ199Hg to Δ201Hg in fish from this study is 1.20 (R2 = 0.998), which is identical to values for marine fish from the Gulf of Mexico and is similar to forage fish in the San Francisco Bay Estuary and the results of laboratory photochemical MMHg degradation experiments. Our results are consistent with deposition of Hg(II) from the atmosphere, methylation at depth in the marine water column (below the mixed layer in the oxygen minimum zone), and decreasing degrees of photodegradation of MMHg with depth in the water column.

  7. CCDC 1061305: Experimental Crystal Structure Determination : Dichloro-(P,P-di-t-butyl-N-(6-(1-methyl-1H-benzimidazol-2-yl)pyridin-2-yl)phosphinous amide)-cobalt dichloro-(P,P-di-t-butyl-N-(6-(1-methyl-1H-benzimidazol-2-yl)pyridin-2-yl)phosphinic amide)-(dimethylformamide)-cobalt dimethylformamide solvate

    KAUST Repository

    Liu, Wen

    2015-01-01

    An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

  8. Degradation of Kresoxim-Methyl in Water: Impact of Varying pH, Temperature, Light and Atmospheric CO2 Level.

    Science.gov (United States)

    Khandelwal, Ashish; Gupta, Suman; Gajbhiye, Vijay T; Varghese, Eldho

    2016-01-01

    In the present investigation, persistence of kresoxim-methyl (a broad spectrum strobilurin fungicide) was studied in water. Results revealed that kresoxim-methyl readily form acid metabolite. Therefore, residues of kresoxim-methyl were quantified on the basis of parent molecule alone and sum total of kresoxim-methyl and its acid metabolite. In water, influence of various abiotic factors like pH, temperature, light and atmospheric carbon dioxide level on dissipation of kresoxim-methyl was studied. The half life value for kresoxim-methyl and total residue varied from 1 to 26.1 and 6.1 to 94.0 days under different conditions. Statistical analysis revealed the significant effect of abiotic factors on the dissipation of kresoxim-methyl from water.

  9. Photocatalytic degradation of methyl green dye in aqueous solution over natural clay-supported ZnO–TiO2 catalysts

    OpenAIRE

    Bel Hadjltaief, Haithem; Ben Zina, Mourad; Galvez, Maria Elena; Da Costa, Patrick

    2016-01-01

    International audience; A ZnO–TiO2/clay photcatalyst was prepared using a natural Tunisian clay as support. Its activity was assayed in the photocatalytic degradation of methyl green in aqueous solutions, in the presence of UVA irradiation. The photocatalyst was synthesized using a metal organic chemical vapor deposition (MOCVD) with Ti (OPri)4 deposed on the natural Na+–clay, followed by a modified sol–gel synthesis method for introduction. The sample was then characterized by scanning elect...

  10. Photocatalytic degradation of Acephate, Omethoate, and Methyl parathion by Fe3O4@SiO2@mTiO2 nanomicrospheres.

    Science.gov (United States)

    Zheng, Lingling; Pi, Fuwei; Wang, Yifan; Xu, Hui; Zhang, Yinzhi; Sun, Xiulan

    2016-09-05

    A novel magnetic mesoporous nanomicrospheres Fe3O4@SiO2@mTiO2 were synthetized and characterized by a series of techniques including FE-TEM, EDS, FE-SEM, PXRD, XPS, BET, TGA as well as VSM, and subsequently tested as a photocatalyst for the degradation of Acephate, Omethoate, and Methyl parathion under UV irradiation. The well-designed nanomicrospheres exhibit a pure and highly crystalline anatase TiO2 layer, large specific surface area, and high-magnetic-response. Photocatalytic degradation of the three organophosphorus pesticides (OPPs) and the formation intermediates were identified using HPLC, TOC-Vcpn, IC, pH meter and GC-MS. Acephate, Omethoate, and Methyl parathion disappeared after 45min, 45min, and 80min UV illumination, respectively. At the end of the treatment, the total organic carbon (TOC) of the OPPs was reduced 80-85%. The main mineralization products were SO4(2-), NO3(-) and PO4(3-) and Omethoate additionally formed NO2(-). Based on the results, we proposed the photocatalytic degradation pathways for Acephate, Omethoate, and Methyl parathion.

  11. Fabrication of efficient visible light activated Cu-P25-graphene ternary composite for photocatalytic degradation of methyl blue

    Science.gov (United States)

    Jin, Zheng; Duan, Wubiao; Liu, Bo; Chen, Xidong; Yang, Feihua; Guo, Jianping

    2015-11-01

    Cu-P25-graphene nanocomposite was fabricated through hydrothermal method at relatively low temperature. The technique used is P25-graphene (PG) binary composite was firstly prepared by P25 and graphite oxide (GO), and then Cu2+ ions were impregnated into PG composite. The prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) spectrum respectively. As the results showed, the Cu-P25-graphene (CPG) nanocomposites possessed the extended light absorption in visible light and better charge separation capability as compared to the pure P25 and PG system. Moreover, CPG-4 (4 mM Cu(NO3)2) showed the highest degradation rate of methyl blue (MB) under the visible light, which the removal efficiency can reach 98% after 100 min. The corresponding hydrogen evolution rate of CPG-4 was 7.9 times than pure P25. It was concluded that the synergistic effects of Cu2+ ions and graphene narrowed the band gap of TiO2 and promoted charge separation, which played significant roles for the enhancement of photoactivity of CPG composite catalysts. In addition, it was observed that the photodegradation of MB followed the first order reaction kinetics. The effects of pH values of MB solution for photocatalysts had also been investigated. The result confirmed that the optimum values of pH were found to be 7. Finally, the stability test of photocatalysts was carried out and the photocatalytic mechanism was explained concretely.

  12. Chemically Methylated and Reduced Pectins: Preparation and Characterisation by 1H-NMR Spectroscopy, Enzymatic Degradation and Gelling Properties

    DEFF Research Database (Denmark)

    Rosenbohm, Christoph; Lundt, Inge; Christensen, T.M.I.E.;

    2003-01-01

    The gelling properties of pectin are known to be closely related to the degree of methylation (DM) and the distribution of the ester groups. In order to investigate this dependency, a natural citrus pectin (DM=64%) has been methylated to pectins with higher DM’s or saponified to achieve pectins...... than with unmodified pectin. The new reduced pectins exhibit high gelling properties. Keywords: Pectin; Methylation; Deesterification; Reduction; DM and DR by 1H-NMR spectroscopy; Reduced Pectin; Pectinases; Gelling properties....

  13. Sonochemical degradation of methyl orange in the presence of Bi2WO6: Effect of operating parameters and the generated reactive oxygen species.

    Science.gov (United States)

    He, Ling-Ling; Liu, Xian-Ping; Wang, Yong-Xia; Wang, Zhi-Xin; Yang, Yan-Jie; Gao, Yan-Ping; Liu, Bin; Wang, Xin

    2016-11-01

    The Bi2WO6 was prepared by the hydrothermal method and its sonocatalytic activity was studied in the degradation of methyl orange (MO) solutions. The effects of catalytic activity of Bi2WO6 on dye were inspected by the change in absorbance of dye with UV-vis spectrometer. The influences of operational parameters such as the addition amount of Bi2WO6, pH, the initial concentration of dyes, ultrasonic power and irradiation time on the degradation ratio were investigated. In addition, the obtained results indicated that the kinetics of sonochemical reactions of MO were consistent with the pseudo first-order kinetics and Bi2WO6 had excellent reusability and stability during the sonochemical degradation processes. The generation and kinds of reactive oxygen species (ROS) and their influence on the sonochemical degradation of MO were determined by the methods of oxidation-extraction spectrophotometry and ROS scavengers. The results indicate that the degradation of MO in the presence of Bi2WO6 under ultrasonic irradiation is related to the generation of ROS, in which both singlet molecular oxygen ((1)O2) and hydroxyl radical (OH) play important roles in the sonochemical degradation of MO. These experimental results provide a sound foundation for the further development of Bi2WO6 as a sonocatalyst in wastewater treatment.

  14. Impact of modified graphene and microwave irradiation on thermal stability and degradation mechanism of poly (styrene-co-methyl meth acrylate)

    Energy Technology Data Exchange (ETDEWEB)

    Zubair, Mukarram [Department of Environmental Engineering, University of Dammam, 31982 Dammam (Saudi Arabia); Shehzad, Farrukh [Department of Chemical Engineering, King Fahd University of Petroleum & Minerals, 31261 Dhahran, Saudi Arabia, (Saudi Arabia); Al-Harthi, Mamdouh A., E-mail: mamdouh@kfupm.edu.sa [Department of Chemical Engineering, King Fahd University of Petroleum & Minerals, 31261 Dhahran, Saudi Arabia, (Saudi Arabia); Center of Research Excellence in Nanotechnology, King Fahd University of Petroleum & Minerals, 31261 Dhahran (Saudi Arabia)

    2016-06-10

    Highlights: • Modified graphene imparts thermal stability to Poly (styrene-co-methyl methacrylate) [P(st-mma)]. • The thermal stability of P(st-mma) decreased with microwave irradiation. • The thermal stability of P(st-mma)/MG nanocomposites increased with irradiation time up to 10 min and decreased subsequently. • The degradation of P(st-mma) and P(st-mma)/MG is governed by random scission model. - Abstract: Poly (styrene-co-methyl methacrylate) [P(st-mma)] composite containing 0.1 wt% modified graphene (MG) was prepared via melt blending. MG was prepared by oxidation method using nitric acid. The P(st-mma) and P(st-mma)MG composite were irradiated using microwave radiation. The degradation mechanism and thermal stability of the irradiated and un-irradiated samples was analyzed by TGA. P(st-mma)MG showed high thermal stability. The average activation energy of thermal degradation was found to be 200 kJ/mol for P(st-mma), 214 kJ/mol for P(st-mma)MG. The activation energy was highest for 10 min irradiated nanocomposites indicating an improvement in stability. The degradation mechanism was investigated by comparing the master plots constructed using the experimental data with theoretical master plots of various kinetic models. The thermal degradation of P(st-mma) and P(st-mma)MG composite before and after irradiation governs the random scission mechanism. SEM and TEM micrographs showed improved interactions and degradation of composites after 10 min and 20 min irradiation respectively.

  15. Fabrication of TiO{sub 2}/MoS{sub 2}@zeolite photocatalyst and its photocatalytic activity for degradation of methyl orange under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Weiping; Xiao, Xinyan, E-mail: cexyxiao@scut.edu.cn; Zheng, Lili; Wan, Caixia

    2015-12-15

    Graphical abstract: A novel approach was developed for fabrication of TiO{sub 2}/MoS{sub 2}@zeolite photocatalyst using bulk MoS{sub 2} as a photosensitizer and zeolite as carrier. The as-prepared TiO{sub 2}/MoS{sub 2}@zeolite composite exhibited excellent photocatalytic performance for degradation of methyl orange under visible-light irradiation. - Highlights: • Ultrasound-exfoliation and hydrothermal reforming technique were employed for generating nano-MoS{sub 2} from micro-MoS{sub 2}. • The embedded sensitizer composite mode of (TiO{sub 2}/MoS{sub 2}/TiO{sub 2}) was used in the fabrication of TiO{sub 2}/MoS{sub 2}@zeolite composite photocatalyst. • The photocatalytic mechanism of TiO{sub 2}/MoS{sub 2}@zeolite photocatalyst was presented. - Abstract: TiO{sub 2}/MoS{sub 2}@zeolite composite photocatalysts with visible-light activity were fabricated via a simple ultrasonic-hydrothermal synthesis method, using TiCl{sub 4} as Ti source, MoS{sub 2} as a direct sensitizer, glycerol water solution with certain dispersion agent as hydrolytic agent, and zeolite as carrier. The structure, morphology, composition, optical properties, and specific surface area of the as-prepared photocatalysts were characterized by using XRD, FTIR, SEM–EDS, TEM, XPS, UV–vis, PL and BET analyzer, respectively. And the photocatalytic degradation of methyl orange (MO) in aqueous suspension has been employed to evaluate the photocatalytic activity and degradation kinetics of as-prepared photocatalysts with xenon lamp as irradiation source. The results indicate that: (1) TiO{sub 2}/MoS{sub 2}@zeolite composite photocatalysts exhibit enhanced photocatalytic activities for methyl orange (MO) degradation compared to Degussa P25; (2) photocatalytic degradation of MO obeys Langmuir–Hinshelwood kinetic model (pseudo-first order reaction), and its degradation rate constant (k{sub app}) (2.304 h{sup −1}) is higher than that of Degussa P25 (0.768 h{sup −1}); (3) the heterostructure

  16. Photo-degradation of Methyl Orange by Polysaccharides/LaFe0.8Cu0.2O3 Composite Films

    Directory of Open Access Journals (Sweden)

    Aojie Deng

    2014-03-01

    Full Text Available The objective of this work was to prepare a series of composite films (polysaccharides with LaFe0.8Cu0.2O3 for the degradation of methyl orange under ultraviolet irradiation. LaFe0.8Cu0.2O3 was prepared by a sol-gel method, and the composite films were obtained by cross-linking reactions between polysaccharides (xylan and chitosan and LaFe0.8Cu0.2O3. Physical and chemical properties of the composite films were investigated by XRD, FTIR, SEM, and BET. Moreover, the influence of the weight ratio of polysaccharide to LaFe0.8Cu0.2O3 on the methyl orange degradation reaction was also studied. Results showed that 67% of the degradation efficiency was achieved within 480 min using chitosan/LaFe0.8Cu0.2O3 (2:1 as photocatalysts, while 58% was for xylan/LaFe0.8Cu0.2O3 (1:1. The difference was due to the variety in the structure of chitosan and xylan.

  17. Visible light induced degradation of methyl orange using β-Ag0.333V2O5 nanorod catalysts by facile thermal decomposition method

    Directory of Open Access Journals (Sweden)

    R. Saravanan

    2015-09-01

    Full Text Available One dimensional nanorods of β-Ag0.333V2O5 have been synthesized by facile thermal decomposition method without using any additives. The prepared sample was characterized by different physical and chemical techniques such as XRD, FE-SEM, TEM, DRS and XPS. The photocatalytic activity of β-Ag0.333V2O5 catalyst was investigated by studying the degradation of methyl orange (MO in aqueous medium under visible light exposure. The result shows β-Ag0.333V2O5 exhibits outstanding photocatalytic activity under visible light illumination.

  18. A Facile Low-Temperature Hydrothermal Method to Prepare Anatase Titania/Cellulose Aerogels with Strong Photocatalytic Activities for Rhodamine B and Methyl Orange Degradations

    Directory of Open Access Journals (Sweden)

    Caichao Wan

    2015-01-01

    Full Text Available A facile low-temperature hydrothermal method for in situ preparation of anatase titania (TiO2 homogeneously dispersed in cellulose aerogels substrates was described. The formed anatase TiO2 aggregations composed of a mass of evenly dispersed TiO2 nanoparticles with sizes of 2−5 nm were embedded in the interconnected three-dimensional (3D architecture of the cellulose aerogels matrixes without large-scale reunion phenomenon; meanwhile, the obtained anatase titania/cellulose (ATC aerogels also had a high loading amount of TiO2 (ca. 35.7%. Furthermore, compared with commercially available Degussa P25, ATC aerogels displayed comparable photocatalytic activities for Rhodamine B and methyl orange degradations under UV radiation, which might be useful in the fields of catalysts, wastewater treatment, and organic pollutant degradation. Meanwhile, the photocatalytic reaction behaviors of ATC aerogels under UV irradiation were also illuminated.

  19. Changes in N-methyl-D-aspartate receptor 2A subunit expression caused by binocular form deprivation and chondroitin sulfate proteoglycan degradation

    Institute of Scientific and Technical Information of China (English)

    Mingming Liu; Wei Qin; Hanping Xie

    2011-01-01

    Light deprivation is known to induce a significant decrease in the percentage of N-methyl-D- aspartate receptor 2A subunit (NR2A)-expressing neurons during development. The purpose of this study was to investigate the effects of binocular form deprivation (BFD) and chondroitin sulfate proteoglycan (CSPG) degradation on NR2A expression via an immunohistochemical study, around the end of a critical developmental period. The results show that the positive staining of NR2A in the normal rat visual cortex increases gradually from postnatal 3-5 weeks (P 0.05). The positive staining of NR2A in the CSPG-treated group was insignificant compared with the BFD group at the same time point from 4 weeks to 7 weeks (P > 0.05). Thus, the effect of BFD on NR2A expression in the rat visual cortex was similar to that of CSPG degradation around the end of the critical developmental period.

  20. Zirconium and silver co-doped TiO2 nanoparticles as visible light catalyst for reduction of 4-nitrophenol, degradation of methyl orange and methylene blue

    Science.gov (United States)

    Naraginti, Saraschandra; Stephen, Finian Bernard; Radhakrishnan, Adhithya; Sivakumar, A.

    2015-01-01

    Catalytic activity of Zr and Ag co-doped TiO2 nanoparticles on the reduction of 4-nitrophenol, degradation of methylene blue and methyl orange was studied using sodium borohydride as reducing agent. The nanoparticles were characterized using X-ray diffraction, energy dispersive X-ray, high resolution transmission electron microscopy, selected area electron diffraction and UV-Vis spectroscopy. The rate of the reduction/degradation was found to increase with increasing amount of the photocatalyst which could be attributed to higher dispersity and small size of the nanoparticles. The catalytic activity of Zr and Ag co-doped TiO2 nanoparticles showed no significant difference even after recycling the catalyst four times indicating a promising potential for industrial application of the prepared photocatalyst.

  1. Zirconium and silver co-doped TiO2 nanoparticles as visible light catalyst for reduction of 4-nitrophenol, degradation of methyl orange and methylene blue.

    Science.gov (United States)

    Naraginti, Saraschandra; Stephen, Finian Bernard; Radhakrishnan, Adhithya; Sivakumar, A

    2015-01-25

    Catalytic activity of Zr and Ag co-doped TiO2 nanoparticles on the reduction of 4-nitrophenol, degradation of methylene blue and methyl orange was studied using sodium borohydride as reducing agent. The nanoparticles were characterized using X-ray diffraction, energy dispersive X-ray, high resolution transmission electron microscopy, selected area electron diffraction and UV-Vis spectroscopy. The rate of the reduction/degradation was found to increase with increasing amount of the photocatalyst which could be attributed to higher dispersity and small size of the nanoparticles. The catalytic activity of Zr and Ag co-doped TiO2 nanoparticles showed no significant difference even after recycling the catalyst four times indicating a promising potential for industrial application of the prepared photocatalyst.

  2. Selection and identification of bacterial strains with methyl-tert-butyl ether, ethyl-tert-butyl ether, and tert-amyl methyl ether degrading capacities.

    Science.gov (United States)

    Purswani, Jessica; Pozo, Clementina; Rodríguez-Díaz, Marina; González-López, Jesús

    2008-11-01

    Nine bacterial strains isolated from two hydrocarbon-contaminated soils were selected because of their capacity for growth in culture media amended with 200 mg/L of one of the following gasoline oxygenates: Methyl-tert-butyl ether (MTBE), ethyl-tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME). These strains were identified by amplification of their 16S rRNA gene, using fDl and rD1 primers, and were tested for their capacity to grow and biotransform these oxygenates in both mineral and cometabolic media. The isolates were classified as Bacillus simplex, Bacillus drentensis, Arthrobacter sp., Acinetobacter calcoaceticus, Acinetobacter sp., Gordonia amicalis (two strains), Nocardioides sp., and Rhodococcus ruber. Arthrobacter sp. (strain MG) and A. calcoaceticus (strain M10) consumed 100 (cometabolic medium) and 82 mg/L (mineral medium) of oxygenate TAME in 21 d, respectively, under aerobic conditions. Rhodococcus ruber (strain E10) was observed to use MTBE and ETBE as the sole carbon and energy source, whereas G. amicalis (strain T3) used TAME as the sole carbon and energy source for growth. All the bacterial strains transformed oxygenates better in the presence of an alternative carbon source (ethanol) with the exception of A. calcoaceticus (strain M10). The capacity of the selected strains to remove MTBE, ETBE, and TAME looks promising for application in bioremediation technologies.

  3. Degradation of Methyl Red in Water by Microwave Radiation and Hydrogen Peroxide%微波/过氧化氢降解水中甲基红

    Institute of Scientific and Technical Information of China (English)

    戴竹青; 王密华; 贾韧刃; 周盼

    2014-01-01

    The synergy effect of microwave/peroxide degradation to the methyl red in water was investigated.The initial concentration of substate,pH,the amount of hydrogen peroxide,reaction time,and temperature were examined respectively, and a mathematical model was established in order to study the degradation of methyl red.The results showed that the degradation was enhanced under alkaline conditions and a longer reaction time.If low residual concentration was demanded with high initial concentration,a high value Z ,the oxidation severity was required.The degradation of methyl red is a first order reaction,of which the reaction rate constant is 0.1 72 4 min-1 and the activation energy is 126.6 kJ/mol.The degradation rate can be as high as 78% in following conditions:initial mass concentration 130 mg/L,volume fraction of hydrogen peroxide 1.6%,reaction at 473 K for 12 min,pH=10.%研究了微波/过氧化氢协同作用下水中甲基红的降解。考察了甲基红初始质量浓度、pH、H 2 O 2加入量、反应时间、温度等因素对降解率和降解量的影响,并建立了甲基红降解的数学模型。结果表明,碱性条件下、反应时间延长有利于甲基红的降解,甲基红初始质量浓度越大,则氧化苛刻度 Z 值越大,甲基红降解反应动力学为一级反应,反应速率常数为0.1724 min-1,降解量的活化能126.6 kJ/mol。在 H 2 O 2加入体积分数为1.6%、甲基红初始质量浓度为130 mg/L、反应温度473 K、反应时间为12 min、pH=10的条件下,甲基红的降解率可达到78%。

  4. Photocatalytic Degradation of Methyl Orange on Bi2O3 and Ag2O-Bi2O3 Nano Photocatalysts

    Directory of Open Access Journals (Sweden)

    Seyed Ali Hosseini

    2017-04-01

    Full Text Available The photocatalytic activity of Bi2O3 and Ag2O-Bi2O3 was evaluated by degradation of aqueous methyl orange as a model dye effluent. Bi2O3 was synthesized using chemical precipitation method. Structural analysis revealed that Bi2O3 contain a unique well-crystallized phase and the average crystallite size of 22.4 nm. The SEM analysis showed that the size of Bi2O3 particles was mainly in the range of 16-22 nm. The most important variables affecting the photocatalytic degradation of dyes, namely reaction time, initial pH and catalyst dosage were studied, and their optimal amounts were found at 60 min, 5.58 and 0.025 g, respectively. A good correlation was found between experimental and predicted responses, confirming the reliability of the model. Incorporation of Ag2O in the structure of composite caused decreasing band gap and its response to visible light. Because a high percentage of sunlight is visible light, hence Ag2O-Bi2O3 nano-composite could be used as an efficient visible light driven photocatalyst for degradation of dye effluents by sunlight. Copyright © 2017 BCREC GROUP. All rights reserved Received: 15th August 2016; Revised: 20th December 2016; Accepted: 21st December 2016 How to Cite: Hosseini, S.A., Saeedi, R. (2017. Photocatalytic Degradation of Methyl Orange on Bi2O3 and Ag2O-Bi2O3 Nano Photocatalysts. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (1: 96-105 (doi:10.9767/bcrec.12.1.623.96-105 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.1.623.96-105

  5. CCDC 1477580: Experimental Crystal Structure Determination : bis(mu-(4-t-butyl-2-(((2-oxy-3,5-dimethylphenyl)sulfanyl)methyl)-6-(((2-oxy-3,5-dimethylphenyl)sulfanyl)methyl)phenolato))-di-iron

    KAUST Repository

    Monica, Francesco Della

    2016-01-01

    An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

  6. Degradation of Methyl Orange and Congo Red dyes by using TiO2 nanoparticles activated by the solar and the solar-like radiation.

    Science.gov (United States)

    Ljubas, Davor; Smoljanić, Goran; Juretić, Hrvoje

    2015-09-15

    In this study we used TiO2 nanoparticles as semiconductor photocatalysts for the degradation of Methyl Orange (MO) and Congo Red (CR) dyes in an aqueous solution. Since TiO2 particles become photocatalytically active by UV radiation, two sources of UV-A radiation were used - natural solar radiation which contains 3-5% UV-A and artificial, solar-like radiation, created by using a lamp. The optimal doses of TiO2 of 500 mg/L for the CR and 1500 mg/L for the MO degradation were determined in experiments with the lamp and were also used in degradation experiments with natural solar light. The efficiency of each process was determined by measuring the absorbance at two visible wavelengths, 466 nm for MO and 498 nm for CR, and the total organic carbon (TOC), i.e. decolorization and mineralization, respectively. In both cases, considerable potential for the degradation of CR and MO was observed - total decolorization of the solution was achieved within 30-60 min, while the TOC removal was in the range 60-90%. CR and MO solutions irradiated without TiO2 nanoparticles showed no observable changes in either decolorization or mineralization. Three different commercially available TiO2 nanoparticles were used: pure-phase anatase, pure-phase rutile, and mixed-phase preparation named Degussa P25. In terms of degradation kinetics, P25 TiO2 exhibited a photocatalytic activity superior to that of pure-phase anatase or rutile. The electric energy consumption per gram of removed TOC was determined. For nearly the same degradation effect, the consumption in the natural solar radiation experiment was more than 60 times lower than in the artificial solar-like radiation experiment.

  7. Spectrophotometric studies of visible light induced photocatalytic degradation of methyl orange using phthalocyanine-modified Fe-doped TiO2 nanocrystals.

    Science.gov (United States)

    Mesgari, Zohreh; Gharagozlou, Mehrnaz; Khosravi, Alireza; Gharanjig, Kamaladin

    2012-06-15

    In this paper, preparation and visible light induced photocatalytic activity of phthalocyanine-modified Fe-doped TiO(2) nanocrystals (Pc/Fe-TiO(2)) with different Fe doping content (0, 0.05, 0.5 and 3.0 mol% Fe) as photocatalysts for the degradation of methyl orange have been reported. The study carried out using XRD, FT-IR, EDX, BET, DRS, UV-Vis, SEM and TEM techniques. Results revealed that modified TiO(2) nanocrystals possessed only the anatase phase with crystal sizes of about 10-23 nm and high surface areas of 2.8-37.3 m(2)/g. It can be seen phthalocyanine and Fe(3+) ion exist in photocatalysts based on analysis of FT-IR and EDX. The doping amount of Fe remarkably affects the activity of modified TiO(2) nanocrystals as catalysts. The 0.5 mol% Fe doping exhibited enhanced photocatalytic activity in this work. It was found that phthalocyanine and Fe induced a shift in the energy band gap to lower energies, which changes from 3.26 to 2.26 eV for pure TiO(2) and Pc/3% Fe-TiO(2) nanocrystals, respectively. Results of the degradation of methyl orange revealed that modified TiO(2) nanocrystals showed much more photocatalytic activity than pure TiO(2) under visible light which makes the applicability of TiO(2) photocatalysts even more versatile.

  8. Biogenic synthesis of Fe3O4 magnetic nanoparticles using Pisum sativum peels extract and its effect on magnetic and Methyl orange dye degradation studies

    Science.gov (United States)

    Prasad, Cheera; Yuvaraja, Gutha; Venkateswarlu, Ponneri

    2017-02-01

    We have been developed facile and ecofriendly method for the synthesis of Fe3O4 magnetic nanoparticles (MNPs) using an aqueous extract of Pisum sativum peels (PS) is used as reducing and capping agent. The as synthesized PS-Fe3O4 MNPs are characterized by diverse techniques such as FTIR, powder XRD, TEM, BET and Raman spectroscopy measurements. The results show that the obtained Fe3O4 nanoparticles exhibits high specific surface area (∼17.6 m2/g) and agglomerated spherical in shape with the size range of 20-30 nm. The magnetic properties of PS-Fe3O4 MNPs sample clearly exhibits ferromagnetic nature with a saturation magnetization of 64.2 emu/g. Further, the catalytic properties of PS-Fe3O4 MNPs for degradation of Methyl orange (MO) dye in aqueous solution have been investigated by UV-visible spectroscopy. The results show that PS-Fe3O4 MNPs is an efficient catalyst for degradation of Methyl orange dye than previously reported ones.

  9. AgI/TiO2 nanocomposites: ultrasound-assisted preparation, visible-light induced photocatalytic degradation of methyl orange and antibacterial activity.

    Science.gov (United States)

    Xue, Bin; Sun, Tao; Wu, Ji-Kui; Mao, Fang; Yang, Wei

    2015-01-01

    AgI/TiO2 nanocomposites were prepared by an ultrasound-assisted precipitation process and subsequent low-temperature (350°C) calcination. The crystal phase, morphology and optical properties of the AgI/TiO2 nanocomposites were characterized by X-ray diffraction, transmission electron microscopy and UV-vis absorption spectroscopy. After calcination, the crystallite size of AgI nanoparticles in the AgI/TiO2 nanocomposites decreased, and visible light absorption intensity of the AgI/TiO2 nanocomposites was significantly enhanced. The AgI/TiO2 nanocomposites after calcination exhibited the superior photocatalytic activity for methyl orange degradation and killing of Escherichia coli under visible light irradiation. The improvement of photocatalytic activity could be attributed to two reasons, namely, reduced crystallite size and enhanced visible light absorption of AgI nanoparticles in calcined AgI/TiO2 nanocomposites. The trapping experiments demonstrated that superoxide radical (O2(-)) and holes (h(+)) were the main reactive species for the photodegradation of methyl orange under visible light irradiation. The ultrasound-assisted preparation approach is efficient and facile, which promotes large-scale production and application of AgI/TiO2 nanocomposites in photocatalytic degradation of organic pollutants, disinfection and other fields.

  10. Magnetic Mn substituted cobalt zinc ferrite systems: Structural, electrical and magnetic properties and their role in photo-catalytic degradation of methyl orange azo dye

    Science.gov (United States)

    Bhukal, Santosh; Bansal, S.; Singhal, Sonal

    2014-07-01

    The present work focuses on the effect of replacement of Fe3+ ions by the Mn3+ ions in cobalt zinc ferrites (Co0.6Zn0.4MnxFe2-xO4 (0.2, 0.4, 0.6, 0.8 and 1.0) on the structural, magnetic, electrical and catalytic properties. Powder X-ray diffraction studies confirmed that all the samples possessed cubic spinel structure with Fd-3m space groups. The saturation magnetization was found to decrease with increase in Mn3+ ions concentration. The drift mobility of all compositions was found to decrease with increase in temperature which could be attributed to the semiconductor nature of nanoferrites. The photo-catalytic activity of all the nanoferrites was evaluated by the degradation of methyl orange dye and it was observed that the degradation of methyl orange dye was enhanced with increase in Mn3+ ions concentration from 0.2 to 1.0. This might be due to the octahedral site preference and higher redox potential of manganese ion as compared those of iron.

  11. Magnetic Mn substituted cobalt zinc ferrite systems: Structural, electrical and magnetic properties and their role in photo-catalytic degradation of methyl orange azo dye

    Energy Technology Data Exchange (ETDEWEB)

    Bhukal, Santosh [Department of Environment Studies, Panjab University, Chandigarh 160014 (India); Bansal, S. [DST, New Delhi (India); Singhal, Sonal, E-mail: sonal1174@gmail.com [Department of Chemistry, Panjab University, Chandigarh 160014 (India)

    2014-07-15

    The present work focuses on the effect of replacement of Fe{sup 3+} ions by the Mn{sup 3+} ions in cobalt zinc ferrites (Co{sub 0.6}Zn{sub 0.4}Mn{sub x}Fe{sub 2−x}O{sub 4} (0.2, 0.4, 0.6, 0.8 and 1.0) on the structural, magnetic, electrical and catalytic properties. Powder X-ray diffraction studies confirmed that all the samples possessed cubic spinel structure with Fd-3m space groups. The saturation magnetization was found to decrease with increase in Mn{sup 3+} ions concentration. The drift mobility of all compositions was found to decrease with increase in temperature which could be attributed to the semiconductor nature of nanoferrites. The photo-catalytic activity of all the nanoferrites was evaluated by the degradation of methyl orange dye and it was observed that the degradation of methyl orange dye was enhanced with increase in Mn{sup 3+} ions concentration from 0.2 to 1.0. This might be due to the octahedral site preference and higher redox potential of manganese ion as compared those of iron.

  12. Successive ratio subtraction coupled with constant multiplication spectrophotometric method for determination of hydroquinone in complex mixture with its degradation products, tretinoin and methyl paraben

    Science.gov (United States)

    Elghobashy, Mohamed R.; Bebawy, Lories I.; Shokry, Rafeek F.; Abbas, Samah S.

    2016-03-01

    A sensitive and selective stability-indicating successive ratio subtraction coupled with constant multiplication (SRS-CM) spectrophotometric method was studied and developed for the spectrum resolution of five component mixture without prior separation. The components were hydroquinone in combination with tretinoin, the polymer formed from hydroquinone alkali degradation, 1,4 benzoquinone and the preservative methyl paraben. The proposed method was used for their determination in their pure form and in pharmaceutical formulation. The zero order absorption spectra of hydroquinone, tretinoin, 1,4 benzoquinone and methyl paraben were determined at 293, 357.5, 245 and 255.2 nm, respectively. The calibration curves were linear over the concentration ranges of 4.00-46.00, 1.00-7.00, 0.60-5.20, and 1.00-7.00 μg mL- 1 for hydroquinone, tretinoin, 1,4 benzoquinone and methyl paraben, respectively. The pharmaceutical formulation was subjected to mild alkali condition and measured by this method resulting in the polymerization of hydroquinone and the formation of toxic 1,4 benzoquinone. The proposed method was validated according to ICH guidelines. The results obtained were statistically analyzed and compared with those obtained by applying the reported method.

  13. 3-Methyl-2-butenal: an enzymatic degradation product of the cytokinin, N-6-(delta-2 isopentenyl)adenine.

    Science.gov (United States)

    Brownlee, B G; Hall, R H; Whitty, C D

    1975-01-01

    An enzyme preparation from immature corn kernels catalyzed cleavage of N-6-(delta-2-isopentenyl)adenine to give the aldehyde, 3-methyl-2-butenal, as the major side-chain derived product. This product, in the form of the semicarbazone, was identical with an authentic product by several criteria: chromatographic behavior, mass and ultraviolet spectra.

  14. Strecker degradation of phenylalanine initiated by 2,4-decadienal or methyl 13-oxooctadeca-9,11-dienoate in model systems.

    Science.gov (United States)

    Zamora, Rosario; Gallardo, Emerenciana; Hidalgo, Francisco J

    2007-02-21

    The reaction of 2,4-decadienal and methyl 13-oxooctadeca-9,11-dienoate with phenylalanine was studied to determine if alkadienals and ketodienes are able to produce the Strecker-type degradation of amino acids to the corresponding Strecker aldehydes. When reactions were carried out at 180 degrees C, both carbonyl compounds degraded phenylalanine to phenylacetaldehyde, among other compounds. The yield of the phenylacetaldehyde produced depended on the reaction pH and increased linearly with both the amount of the lipid and the reaction time. The yield of this conversion was approximately 8% when starting from decadienal and approximately 6% when starting from methyl 13-oxooctadeca-9,11-dienoate, and the reaction rate was lower for the ketone than for the aldehyde. Simultaneous to these reactions, the lipid was converted into pyrrole, pyridine, or aldehyde derivatives as a result of several competitive reactions. In particular, 9-14% of the decadienal was converted into hexanal under the assayed conditions. All these reactions are suggested to be produced as a consequence of the oxidation of the alkadienal or the ketodiene to the corresponding epoxyalkenal or unsaturated epoxyketone, which were identified in the reaction mixtures by GC-MS. All these results suggest that alkadienals and ketodienes, which are quantitatively important secondary lipid oxidation products, can degrade amino acids to their corresponding Strecker aldehydes. Therefore, under appropriate conditions, these products are not final products of the lipid oxidation and can participate in carbonyl-amine reactions analogously to other lipid oxidation products with two oxygenated functions.

  15. Hepatitis C virus core protein inhibits E6AP expression via DNA methylation to escape from ubiquitin-dependent proteasomal degradation.

    Science.gov (United States)

    Kwak, Juri; Shim, Joo Hee; Tiwari, Indira; Jang, Kyung Lib

    2016-09-28

    The E6-associated protein (E6AP) is a ubiquitin ligase that mediates ubiquitination and proteasomal degradation of hepatitis C virus (HCV) core protein. Given the role of HCV core protein as a major component of the viral nucleocapsid, as well as a multifunctional protein involved in viral pathogenesis and hepatocarcinogenesis, HCV has likely evolved a strategy to counteract the host anti-viral defense mechanism of E6AP and maximize its potential to produce infectious virus particles. In the present study, we found that HCV core protein derived from either ectopic expression or HCV infection inhibits E6AP expression via promoter hypermethylation in human hepatocytes. As a result, the potential of E6AP to ubiquitinate and degrade HCV core protein through the ubiquitin-proteasome system was severely impaired, which in turn led to stimulation of virus propagation. The effects of HCV core protein were almost completely abolished when the E6AP level was restored by ectopic expression of E6AP, treatment with a universal DNA methyltransferase (DNMT) inhibitor, 5-Aza-2'dC, or knock-down of DNMT1. In conclusion, HCV core protein inhibits E6AP expression via DNA methylation to protect itself from ubiquitin-dependent proteasomal degradation and stimulate virus propagation, providing a potential target for the development of anti-viral drugs against HCV.

  16. Optimization of photocatalytic degradation of methyl blue using silver ion doped titanium dioxide by combination of experimental design and response surface approach.

    Science.gov (United States)

    Sahoo, C; Gupta, A K

    2012-05-15

    Photocatalytic degradation of methyl blue (MYB) was studied using Ag(+) doped TiO(2) under UV irradiation in a batch reactor. Catalytic dose, initial concentration of dye and pH of the reaction mixture were found to influence the degradation process most. The degradation was found to be effective in the range catalytic dose (0.5-1.5g/L), initial dye concentration (25-100ppm) and pH of reaction mixture (5-9). Using the three factors three levels Box-Behnken design of experiment technique 15 sets of experiments were designed considering the effective ranges of the influential parameters. The results of the experiments were fitted to two quadratic polynomial models developed using response surface methodology (RSM), representing functional relationship between the decolorization and mineralization of MYB and the experimental parameters. Design Expert software version 8.0.6.1 was used to optimize the effects of the experimental parameters on the responses. The optimum values of the parameters were dose of Ag(+) doped TiO(2) 0.99g/L, initial concentration of MYB 57.68ppm and pH of reaction mixture 7.76. Under the optimal condition the predicted decolorization and mineralization rate of MYB were 95.97% and 80.33%, respectively. Regression analysis with R(2) values >0.99 showed goodness of fit of the experimental results with predicted values.

  17. Solar photocatalytic degradation of mono azo methyl orange and diazo reactive green 19 in single and binary dye solutions: adsorbability vs photodegradation rate.

    Science.gov (United States)

    Ong, Soon-An; Min, Ohm-Mar; Ho, Li-Ngee; Wong, Yee-Shian

    2013-05-01

    The objective of this study was to examine the effects of adsorbability and number of sulfonate group on solar photocatalytic degradation of mono azo methyl orange (MO) and diazo Reactive Green 19 (RG19) in single and binary dye solutions. The adsorption capacity of MO and RG19 onto the TiO₂ was 16.9 and 26.8 mg/g, respectively, in single dye solution, and reduced to 5.0 and 23.1 mg/g, respectively, in the binary dye solution. The data obtained for photocatalytic degradation of MO and RG19 in single and binary dye solution were well fitted with the Langmuir-Hinshelwood kinetic model. The pseudo-first-order rate constants of diazo RG19 were significant higher than the mono azo MO either in single or binary dye solutions. The higher number of sulfonate group in RG19 contributed to better adsorption capacity onto the surface of TiO₂ than MO indicating greater photocatalytic degradation rate.

  18. Solubilities of 1,2,3-trimethylbenzene and 1,2,4-trimethylbenzene and 1,3,5-trimethylbenzene in t-butyl alcohol + water mixtures and hydrophobic interaction

    Institute of Scientific and Technical Information of China (English)

    邹立壮; 杨冠英; 韩布兴; 刘瑞麟; 阎海科

    1999-01-01

    The solubilities of 1,2,3- trimethylbenzene, 1,2,4-trimethylbenzene and 1,3,5-trimethylbenzene in mixed solvents of t-butyl alcohol (TBA) and water at 283.15, 288.15, 293.15 and 298.15 K have been determined by spectrophotometry. The mole fractions of TBA [x(TBA)] in the mixed solvent are 0.000, 0.010, 0.020, 0.030, 0.040, 0.045, 0.050, 0.060, 0.080 and 0. 1000. The Gibbs energies of hydrophobie interaction (HI) for the aggregating process of three methane molecules with one benene molecule in the mixed solvent are studied, and the effect of solvent structure and solute aggregating state on the strength of HI is discussed.

  19. Identification of oxidative degradates of the thrombin inhibitor, 3-(2-phenethylamino)-6-methyl-1-(2-amino-6-methyl-5-methyleneca rboxamidomethylpyridinyl)pyrazinone, using liquid chromatography/mass spectrometry and liquid chromatography/tandem mass spectrometry.

    Science.gov (United States)

    Wu, Y; Chen, X; Gier, L; Almarsson, O; Ostovic, D; Loper, A E

    1999-07-01

    Liquid chromatography/mass spectrometry was used to identify reaction products from a solution of 3-(2-phenethylamino)-6-methyl-1-(2-amino-6-methyl-5-methyleneca rboxamidomethylpyridinyl)pyrazinone (L-375,378) and hydrogen peroxide, a system that generates high levels of the oxidative degradates which form in the tablets and intravenous (i.v.) solutions of L-375,378. Two major hydrogen peroxide reaction products of L-375,378 (m/z 407) with m/z values of 369 and 370 were separated and identified. Both compounds were products of ring opening with elimination of three carbon atoms from the center pyrazinone ring. The structural assignments for these two products were alpha-amidinoamide and alpha-diamide compounds, respectively. In addition, five products (m/z 423) with a molecular weight 16 Da greater than that for L-375,378 were separated. Further liquid chromatography/tandem mass spectrometry experiments indicated that three of these M + 16 products were phenolic derivatives of L-375,378. Among them, the para-hydroxy compound has been verified using an authentic standard. The other two phenolic compounds were believed to be the meta- and ortho-hydroxy derivatives of L-375,378. The fourth M + 16 product was derived from hydroxylation of the methyl group on the center pyrazinone ring. The fifth M + 16 product was derived from oxidation on the aminopyridine moiety, most likely N-oxide of the pyridine ring. Other minor hydrogen peroxide reaction products were not studied in detail because they did not appear in tablets or i.v. formulations.

  20. Synthesis of Ag-ZnO with multiple rods (multipods) morphology and its application in the simultaneous photo-catalytic degradation of methyl orange and methylene blue.

    Science.gov (United States)

    Arab Chamjangali, M; Bagherian, G; Javid, A; Boroumand, S; Farzaneh, N

    2015-11-05

    In this study, the photo-decolorization of a mixture of methylene blue (MB) and methyl orange (MO) was investigated using Ag-ZnO multipods. The photo-catalyst used, ZnO multipods, was successfully synthesized. The surface of ZnO microstructure was modified by deposition of different amounts of Ag nanoparticles (Ag NPs) using the photo-reduction method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis and atomic absorption spectroscopy. The photo-catalytic efficiency of Ag-ZnO is mainly controlled by the amount of Ag NPs deposited on the ZnO surface. The results obtained suggest that Ag-ZnO containing 6.5% Ag NPs, has the highest photo-catalytic performance in the simultaneous photo-degradation of dyes at a shorter time.

  1. PhotoCatalytic Degradation of Methyl Blue Dye and Enhanced Antibacterial Properties of Treated Wool with ZrCL4 and Dyeing with Madder

    Directory of Open Access Journals (Sweden)

    Arash Almasian

    2015-03-01

    Full Text Available This research aims to create the photo catalytic degradation of methyl blue dye and enhanced antibacterial properties on wool fabric using ZrCl4 particles. Wool fabrics were treated with different concentrations of zirconium salt in water solution including %1, %3, %6 and 9% o.w.f. and the dyeing process was carried out on the fabrics in the states before, simultaneously and after the mordanting with madder.Formic acid was used to generate acidic pH.The photo catalytic properties of the fabrics were examined through evaluating the color removal from the stained fabric with Methylene Blue. The antibacterial properties were determined by reduction growth of a Gram-negative bacterium E. coli and a Gram-positive bacterium Staphylococcus aureus. Furthermore, the FTIR spectrum of some samples was analyzed. The SEM pictures and EDX spectrums of some samples were also reported.

  2. Fabrication and characterization of CdS doped TiO2 nanotube composite and its photocatalytic activity for the degradation of methyl orange.

    Science.gov (United States)

    Chung, Jinwook; Kim, Seu-Run; Kim, Jong-Oh

    2015-01-01

    CdS doped TiO2 nanotube composite was fabricated by chemical bath deposition, and was characterized by the structural, spectral and photoelectrochemical properties. The results of the structural and spectral properties showed that CdS particles were successfully deposited onto the surface of TiO2 nanotube. It is demonstrated that CdS doped TiO2 nanotube composite improved the light harvesting ability. Power conversion efficiency of about 0.32% was observed. This value is about 2.9 times higher than that of pure TiO2 nanotube. The CdS doped TiO2 nanotube composite possesses relatively higher photocatalytic activity and photodegradation efficiency than that of pure TiO2 nanotube under UV light irradiation, and the degradation efficiency of methyl orange was about 42% at UV intensity of 32 W.

  3. Sono-chemical Synthesis Fe3O4-Mg(OH2 Nanocomposite and Its Photo-catalyst Investigation in Methyl Orange Degradation

    Directory of Open Access Journals (Sweden)

    G. Nabiyouni

    2014-10-01

    Full Text Available In this work firstly Fe3O4 nanoparticles were synthesized via a sono-chemical method. At the second step magnesium hydroxide shell was synthesized on the magnetite-core under ultrasonic waves. For preparation Fe3O4-MgO the product was calcinated at 400 ºC for 2h. Properties of the product were examined by X-ray diffraction pattern (XRD, scanning electron microscope (SEM and Fourier transform infrared (FT-IR spectroscopy. Vibrating sample magnetometer (VSM shows nanoparticles exhibit super-paramagnetic behavior. The photo-catalytic behavior of Fe3O4-Mg(OH2  nanocomposite was evaluated using the degradation of a methyl orange (MeO aqueous solution under ultraviolet (UV light irradiation. The results show that Fe3O4-Mg(OH2 nanocomposites have applicable magnetic and photo-catalytic performance.

  4. Synergistic effect of nanocavities in anatase TiO2 nanobelts for photocatalytic degradation of methyl orange dye in aqueous solution.

    Science.gov (United States)

    Praveen Kumar, D; Lakshmana Reddy, N; Karthikeyan, M; Chinnaiah, N; Bramhaiah, V; Durga Kumari, V; Shankar, M V

    2016-09-01

    Nanocavities are empty voids exposed on the surface of one dimensional TiO2 nanostructured material. Often, they exhibited beneficial optical and electrical properties that leads to efficient photocatalytic reactions. This study reports formation of nanocavities on anatase TiO2 nanobelts (TNB) through dehydroxylation of surface hydroxyl groups during calcination process (350-600°C). The morphological and crystal structure analysis of TNB-500, -550 and -600 displayed the nanobelts shape with high density of nano-size cavities and increase in average diameter with calcination temperature. The SAED patterns confirm the anatase TiO2 phase. The enhanced light absorption properties of biphasic anatase/TiO2-B and anatase TiO2 than H2Ti3O7 are attributed to transformation of crystal structure upon calcination process. The catalytic activity was evaluated for degradation of methyl orange dye in aqueous solution under solar light irradiation. The reaction variables such as calcination temperature, amount of catalyst and pH of the methyl orange dye solution were studied and discussed in detail. Under optimal experimental conditions TNB-550 photocatalyst displayed highest degradation performance about 8 folds higher than H2Ti3O7. The high performance is explained as due to synergistic properties of one dimensional anatase TiO2 with high density of nanocavities leading to one dimensional transfer of electrons and high absorption co-efficient in UV-A spectrum are suitable for efficient red-ox reactions. Copyright © 2016 Elsevier Inc. All rights reserved.

  5. Altered methylation and expression of ER-associated degradation factors in long-term alcohol and constitutive ER stress-induced murine hepatic tumors

    Directory of Open Access Journals (Sweden)

    Hui eHan

    2013-10-01

    Full Text Available Mortality from liver cancer in humans is increasingly attributable to heavy or long-term alcohol consumption. The mechanisms by which alcohol exerts its carcinogenic effect are not well understood. In this study, the role of alcohol-induced endoplasmic reticulum (ER stress response in liver cancer development was investigated using an animal model with a liver knockout of the chaperone BiP and under constitutive hepatic ER stress. Long-term alcohol and high fat diet (HFD feeding resulted in higher levels of serum alanine aminotransferase (ALT, impaired ER stress response, and higher incidence of liver tumor in older (aged 16 months knockout females than in either middle-aged (6 months knockouts or older (aged 16 months wild type females. In the older knockout females, stronger effects of the alcohol on methylation of CpG islands at promoter regions of genes involved in the ER associated degradation (ERAD were also detected. Altered expression of ERAD factors including derlin 3, Creld2 (cysteine-rich with EGF-like domains 2, Herpud1 (ubiquitin-like domain member, Wfs1 (wolfram syndrome gene, and Yod1 (deubiquinating enzyme 1 was co-present with decreased proteasome activities, increased estrogen receptor alpha variant (ERa36, and enhanced phosphorylations of ERK1/2 (extracellular signal-regulated protein kinases 1 and 2 and STAT3 (the signal transducers and activators of transcription in the older knockout female fed alcohol. Our results suggest that long-term alcohol consumption and ageing may promote liver tumorigenesis in females through interfering with DNA methylation and expression of genes involved in the ER associated degradation.

  6. Enhanced Photocatalytic Degradation of Methyl Orange Dye under the Daylight Irradiation over CN-TiO2 Modified with OMS-2

    Directory of Open Access Journals (Sweden)

    Mohamed Elfatih Hassan

    2014-12-01

    Full Text Available In this study, CN-TiO2 was modified with cryptomelane octahedral molecular sieves (OMS-2 by the sol-gel method based on the self-assembly technique to enhance its photocatalytic activity under the daylight irradiation. The synthesized samples were characterized by X-ray diffraction (XRD, UV-vis spectroscopy, Fourier transform infrared spectroscopy (FT-IR and porosimeter analysis. The results showed that the addition of OMS-2 in the sol lead to higher Brunauer-Emmett-Teller (BET surface area, pore volume, porosity of particle after heat treatment and the specific surface area, porosity, crystallite size and pore size distribution could be controlled by adjusting the calcination temperature. Compared to the CN-TiO2-400 sample, CN-TiO2/OMS-2-400 exhibited greater red shift in absorption edge of samples in visible region due to the OMS-2 coated. The enhancement of photocatalytic activity of CN-TiO2/OMS-2 composite photocatalyst was subsequently evaluated for the degradation of the methyl orange dye under the daylight irradiation in water. The results showed that the methyl orange dye degradation rate reach to 37.8% for the CN-TiO2/OMS-2-400 sample under the daylight irradiation for 5 h, which was higher than that of reference sample. The enhancement in daylight photocatalytic activities of the CN-TiO2/OMS samples could be attributed to the synergistic effects of OMS-2 coated, larger surface area and red shift in adsorption edge of the prepared sample.

  7. Residue and Degradation Analysis of Isofenphos-methyl in Soil%甲基异柳磷在土壤中的残留降解分析

    Institute of Scientific and Technical Information of China (English)

    费仁雷; 张滢; 张化平; 张雅静; 李婧

    2016-01-01

    该实验应用气相色谱法测定了土壤中的甲基异柳磷的残留降解情况,以丙酮-正己烷(2∶1,V/V)为提取剂,氮吹仪浓缩定容,经气相色谱外标法定量测定。结果表明,当添加水平为0.05mg/kg时,甲基异柳磷在土壤中的回收率为91.33%,添加水平为0.1mg/kg时回收率为100.5%;添加浓度0.1mg/kg的甲基异柳磷在土壤中半衰期为9.58~11.27d。%A experiment was conducted to reveal residual and degradation of Isofenphos-methyl in soil. The residues in the samples were extracted by mixture of acetone and hexane,then,samples were prepared after concentrition and constant volume,the target compounds were determined by GC as external standart. The spiked recoveries of Isofen⁃phos-methyl in soil were 91.33%at the spiked level of 0.05mg/kg and 100.5%at the spiked levels of 0.1mg/kg. The results showed that the half-live of Isofenphos-methyl in soil was 9.58~11.27d.

  8. Wavelength-sensitive photocatalytic degradation of methyl orange in aqueous suspension over iron(III)-doped TiO2 nanopowders under UV and visible light irradiation.

    Science.gov (United States)

    Wang, X H; Li, J-G; Kamiyama, H; Moriyoshi, Y; Ishigaki, T

    2006-04-06

    Well-crystallized iron(III)-doped TiO2 nanopowders with controlled Fe3+ doping concentration and uniform dopant distribution, have been synthesized with plasma oxidative pyrolysis. The photocatalytic reactivity of the synthesized TiO2 nanopowders with a mean particle size of 50-70 nm was quantified in terms of the degradation rates of methyl orange (MO) in aqueous TiO2 suspension under UV (mainly 365 and 316 nm) and visible light irradiation (mainly 405 and 436 nm). The photodecomposition of MO over TiO2 nanopowders followed a distinct two-stage pseudo first order kinetics. Interestingly, the photocatalytic reactivity depends not only on the iron doping concentration but also on the wavelength of the irradiating light. Under UV irradiation, nominally undoped TiO2 had much higher reactivity than Fe3+ -doped TiO2, suggesting that Fe3+ doping (> 0.05 at. %) in TiO2 with a mean particle size of approximately 60 nm was detrimental to the photocatalytic decomposition of methyl orange. Whereas, under visible light irradiation, the Fe3+ -doped TiO2 with an intermediate iron doping concentration of approximately 1 at. % had the highest photocatalytic reactivity due to the narrowing of band gap so that it could effectively absorb the light with longer wavelength. A strategy for improving the photocatalytic reactivity of Fe3+ -doped TiO2 used in the visible light region is also proposed.

  9. Photocatalytic degradation of methyl orange: influence of H2O2 in the TiO2-based system.

    Science.gov (United States)

    Andronic, Luminita; Manolache, Simona; Duta, Anca

    2008-02-01

    The purpose of this study was to investigate the photocatalytic oxidation of a reactive azo dye. The photocatalytic activity of the TiO2 was studied using a reactor equipped with UV-A sources, with maximum emission at 365 nm. The photocatalytic activity of the TiO2 powder (99.9% anatase) and thin films has been measured through the decomposition of methyl orange solutions. The thin film was prepared by doctor blade and spray pyrolysis deposition (SPD). The TiO2 suspensions were prepared at 1 g/L concentration, and the initial methyl orange concentration was fixed at 7.8125 mg/L. The influence of the TiO2 (powder or thin films) and/or O2 and H2O2 on the photobleaching rate, was tested under different experiments, at pH = 5. Thin films (doctor blade) of TiO2 formed of mezo-sized aggregates formed of nanosized anatase crystallites show better photobleaching efficiency than thin film (SPD) due to their large internal surface. The rate is even higher in H2O2 compared to oxygen environment.

  10. Lanthanum and boron co-doped BiVO4 with enhanced visible light photocatalytic activity for degradation of methyl orange

    Institute of Scientific and Technical Information of China (English)

    王敏; 车寅生; 牛超; 党明岩; 董多

    2013-01-01

    BiVO4 photocatalysts co-doped with La and B were prepared by sol-gel method using citric acid as chelate. The samples were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), Bru-mauer-Emmett-Teller (BET), UV-Vis diffuse reflectance spectra (DRS) and the photocatalytic activity was investigated by photo-catalytic degradation of methyl orange (MO). The results showed that boron and lanthanum ions incorporated into the lattice of BiVO4, and co-doping led to more surface oxygen vacancies, high specific surface areas, small crystallite size, narrow band gap and intense light absorbance in visible region. And the doped La(III) ions could help the separation of photogenerated electrons. Com-pared with BiVO4 and B-BiVO4, the photocatalytic activity of La-B co-doped BiVO4 was remarkably improved due to the synergistic effects of the co-doped ions. The degradation rate of MO in 60 min was 98.4%when La doping content was 0.05 mol.%, which was much higher than that of pure BiVO4(20%) and B-BiVO4(37%).

  11. Enhanced photocatalytic activity of nanocomposites of TiO2 doped with Zr, Y or Ce polyoxometalates for degradation of methyl orange dye.

    Science.gov (United States)

    Khoshnavazi, Roushan; Fereydouni, Shler; Bahrami, Leila

    2016-01-01

    The synergistic effect of polyoxometalate (POM) and metal-doped TiO2 (metal = Zr, Y and Ce) was examined, to fabricate nanocomposites with enhanced photocatalytic activities toward the degradation of methyl orange (MO), as a model textile dye. A series of new nanocomposites, containing different loading amounts of H9Na3[WZn3(H2O)2(ZnW9O34)2].24H2O (HZnW) (10-30%) on each of the metal-doped TiO2 nanoparticles, were synthesized using impregnation method. The morphology and crystal phase of the as-prepared nanocomposites were investigated by various characterization techniques: Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray analysis and diffuse reflectance spectroscopy, indicating that the HZnW and metal-doped TiO2 had been successfully incorporated into the nanocomposite structure. The effects of parameters such as loading amount of HZnW, catalyst dose, pH and initial concentration of dye solution were investigated on the degradation kinetics and it was interestingly found that the prepared nanocomposites could efficiently degrade the MO dye in 5-7 min under UV light irradiation. The best results were obtained for the HZnW-Zr-TiO2 among the different nanocomposites. Also, control studies showed the superior photocatalytic properties of composites compared to that of the individual components. The facile preparation and their improved photocatalytic activities suggest that these materials can have a promising future for water and wastewater purifications.

  12. Cellular uptake and degradation behaviour of biodegradable poly(ethylene glycol-graft-methyl methacrylate) nanoparticles crosslinked with dimethacryloyl hydroxylamine.

    Science.gov (United States)

    Scheler, Stefan; Kitzan, Martina; Fahr, Alfred

    2011-01-17

    Crosslinked polymers with hydrolytically cleavable linkages are highly interesting materials for the design of biodegradable drug carriers. The aim of this study was to investigate if nanoparticles made of such polymers have the potential to be used also for intracellular drug delivery. PEGylated nanoparticles were prepared by copolymerization of methacrylic acid esters and N,O-dimethacryloylhydroxylamine (DMHA). The particles were stable at pH 5.0. At pH 7.4 and 9.0 the degradation covered a time span of about 14 days, following first-order kinetics with higher crosslinked particles degrading slower. Cellular particle uptake and cytotoxicity were tested with L929 mouse fibroblasts. The particle uptake rate was found to correlate linearly with the surface charge and to increase as the zeta potential becomes less negative. Coating of the particle surface with polysorbate 80 drops the internalization rate close to zero and the charge dependence disappears. This indicates the existence of a second effect apart from surface charge. A similar pattern of correlation with zeta potential and coating was also found for the degree of membrane damage while there was no effect of polysorbate on the cell metabolism which increased as the negative charge decreased. It is discussed whether exocytotic processes may explain this behaviour.

  13. Bacterial degradation of tert-amyl alcohol proceeds via hemiterpene 2-methyl-3-buten-2-ol by employing the tertiary alcohol desaturase function of the Rieske nonheme mononuclear iron oxygenase MdpJ.

    Science.gov (United States)

    Schuster, Judith; Schäfer, Franziska; Hübler, Nora; Brandt, Anne; Rosell, Mònica; Härtig, Claus; Harms, Hauke; Müller, Roland H; Rohwerder, Thore

    2012-03-01

    Tertiary alcohols, such as tert-butyl alcohol (TBA) and tert-amyl alcohol (TAA) and higher homologues, are only slowly degraded microbially. The conversion of TBA seems to proceed via hydroxylation to 2-methylpropan-1,2-diol, which is further oxidized to 2-hydroxyisobutyric acid. By analogy, a branched pathway is expected for the degradation of TAA, as this molecule possesses several potential hydroxylation sites. In Aquincola tertiaricarbonis L108 and Methylibium petroleiphilum PM1, a likely candidate catalyst for hydroxylations is the putative tertiary alcohol monooxygenase MdpJ. However, by comparing metabolite accumulations in wild-type strains of L108 and PM1 and in two mdpJ knockout mutants of strain L108, we could clearly show that MdpJ is not hydroxylating TAA to diols but functions as a desaturase, resulting in the formation of the hemiterpene 2-methyl-3-buten-2-ol. The latter is further processed via the hemiterpenes prenol, prenal, and 3-methylcrotonic acid. Likewise, 3-methyl-3-pentanol is degraded via 3-methyl-1-penten-3-ol. Wild-type strain L108 and mdpJ knockout mutants formed isoamylene and isoprene from TAA and 2-methyl-3-buten-2-ol, respectively. It is likely that this dehydratase activity is catalyzed by a not-yet-characterized enzyme postulated for the isomerization of 2-methyl-3-buten-2-ol and prenol. The vitamin requirements of strain L108 growing on TAA and the occurrence of 3-methylcrotonic acid as a metabolite indicate that TAA and hemiterpene degradation are linked with the catabolic route of the amino acid leucine, including an involvement of the biotin-dependent 3-methylcrotonyl coenzyme A (3-methylcrotonyl-CoA) carboxylase LiuBD. Evolutionary aspects of favored desaturase versus hydroxylation pathways for TAA conversion and the possible role of MdpJ in the degradation of higher tertiary alcohols are discussed.

  14. Preparation, characterization of Y3+-doped TiO2 nanoparticles and their photocatalytic activities for methyl orange degradation

    Institute of Scientific and Technical Information of China (English)

    NIU Xinshu; LI Sujuan; CHU Huihui; ZHOU Jianguo

    2011-01-01

    A series of pure and Y3+-doped TiO2 nanoparticles with high photocatalytic activities were prepared by a sol-gel method using tetra-n-butyl titanate as precursor. The as-prepared catalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and diffuse reflectance spectroscopy (DRS). The results indicated that yttrium doping could effectively reduce the crystalline size, inhibit the anatase-to-tutile phase transformation and surppress the recombination of the photogenerated electron-hole pairs. The DRS results showed that the optical absorption edge shifted to red direction owing to yttrium ion doping. The photocatalytic activities of samples were evaluated by the photodegradation of methyl orange (MO) aqueous solution under 300 W high pressure mercury lamp irradiation. Photodegradation results revealed that Y3+ doping could greatly improve the photocatalytic activity of TiO2. In this experiment, the optimal dosage was 1 .5 mol.% when samples were calcined at 773 K for 2 h, which caused a MO photodegradation rate of 99.8% under UV irradiation for 70 min.

  15. Titanium Dioxide Supported on Different Porous Materials as Photocatalyst for the Degradation of Methyl Green in Wastewaters

    Directory of Open Access Journals (Sweden)

    Haithem Bel Hadjltaief

    2015-01-01

    Full Text Available TiO2 nanoparticles were immobilized on two porous materials used as catalyst supports, namely, activated carbon (AC and natural clay (NC, through an impregnation process using TiO2 (P25 as precursor. The so-prepared composite materials were characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, transition electron microscopy (TEM, and nitrogen physisorption, that is, Brunauer-Emmett-Teller (BET surface area determination. SEM and TEM observation evidenced that TiO2 was deposited on AC and NC surface. XRD results confirmed that TiO2 existed in a mixture of anatase and rutile phases. The specific surface area of photocatalysts decreased drastically in comparison with the original materials. The photocatalytic activity of these materials was assayed in the oxidation of Methyl Green (MG dye in aqueous medium under UV irradiation. TiO2/AC exhibited higher photocatalytic oxidation activity than TiO2 at neutral pH. Total mineralization of MG was confirmed by means of COD analysis, pointing to these materials as an efficient, cost-effective, and environment friendly alternative for water treatment.

  16. Remarkable catalytic activity of Bi2O3/TiO2 nanocomposites prepared by hydrothermal method for the degradation of methyl orange

    Science.gov (United States)

    Malligavathy, M.; Iyyapushpam, S.; Nishanthi, S. T.; Pathinettam Padiyan, D.

    2017-04-01

    Visible light Bi2O3/TiO2 nanocomposites are successfully prepared with different dosages of Bi2O3 by hydrothermal process. All the as-prepared samples are characterized by X-ray diffraction (XRD), scanning and transmission electron microscopes (SEM and TEM), Brunauer-Emmett-Teller analysis (BET), N2 adsorption-desorption measurement, and UV-Vis diffuse reflectance spectra (DRS). XRD and Raman spectra reveal the anatase phase of both TiO2 and Bi2O3/TiO2 nanocomposites. X-ray diffraction patterns demonstrate that the bismuth ions did not enter into the lattice of TiO2, and Bi2O3 is extremely dispersive on the surface of TiO2 nanoparticles. The incorporation of Bi2O3 in TiO2 leads to the spectral response of TiO2 in the visible light region and efficient separation of charge carriers. The enhanced visible light activity is tested by the photocatalytic degradation of methyl orange under light illumination, and the performance of Bi2O3/TiO2 nanocomposites are superior than that of pure TiO2 which is ascribed to the efficient charge separation and transfer across the Bi2O3/TiO2 junction. Bi2O3/TiO2 nanocomposite (20 mg) loaded with 0.25 of Bi2O3 dispersed in 50 ml of 5 ppm methyl orange solution exhibited the highest photocatalytic activity of 98.86% within 240 min of irradiation, which is attributed to the low band gap, high surface area, and the strong interaction between Bi2O3 and TiO2.

  17. Kinetic study of degradation of methyl orange on TiO_2 film%TiO_2薄膜降解甲基橙动力学研究

    Institute of Scientific and Technical Information of China (English)

    贾彩云; 吴迪

    2012-01-01

    采用450 W汞灯做光源,对TiO2薄膜光催化氧化甲基橙进行动力学研究。结果显示:TiO2薄膜光催化氧化甲基橙的动力学可用Langmuir-Hinshelwood(L-H)方程描述。甲基橙初始浓度≤20 mg/L时,TiO2薄膜光催化氧化甲基橙表现为一级反应;甲基橙初始浓度≥24 mg/L时,则表现为零级反应。%Using 450W mercury lamp as light source,the kinetics of degradation of methyl orange with TiO2 thin films were studied.The results showed that the degradation rate of methyl orange solution could be described by the Langmuir-Hinshelwood(L-H) kinetic equation.As the original concentration of methyl orange less than or equal to 20 mg/L,the photocatalytic oxidation of methyl orange on TiO2 films followed the first-order reaction kinetics;and after more than 24 mg/L,the methyl orange reaction turned to a zero-order reaction.

  18. Increase in in utero exposure to a migrant, 4,4'-butylidenebis(6-t-butyl-m-cresol), from nitrile-butadiene rubber gloves on brain aromatase activity in male rats.

    Science.gov (United States)

    Satoh, Kanako; Nonaka, Ryouichi; Nakae, Dai; Ogata, Akio

    2010-01-01

    4,4'-Butylidenebis(6-t-butyl-m-cresol) (BBBC) can be eluted from disposable gloves made of nitrile-butadiene rubber and possibly also detected in food. It has been reported that BBBC is an androgen and estrogen antagonist in vitro. Previously, BBBC (1.0 mg/kg body weight (bw)/d) was subcutaneously administered to pregnant rats from gestation days 11 through 18, and the effects on male offspring (postnatal day 102) were examined. Altered levels and turnover of the monoamines dopamine, serotonin, and noradrenalin as well as their metabolites were detected. This report measured the level of serum testosterone following prenatal exposure to BBBC (0.1, 1.0, 10 mg/kg bw/d) in male rats, and measured aromatase activity of the hypothalamus-preoptic area with a close connection to the sexual differentiation and sexual behavior of BBBC-treated rat brains. The serum testosterone level rose depending on exposure, and aromatase activity of the basomedial nucleus of amygdale region was increased in the BBBC-treated group compared with the control. These results suggested that prenatal exposure to BBBC affects the central nervous system of male rat offspring, and BBBC may be an endocrine disrupting-chemical during the fetal period, and might influence the functional development of the brain.

  19. Hydrogen bonded NHO chains formed by chloranilic acid (CLA) with 4,4‧-di-t-butyl-2,2‧-bipyridyl (dtBBP) in the solid state

    Science.gov (United States)

    Bator, G.; Sawka-Dobrowolska, W.; Sobczyk, L.; Owczarek, M.; Pawlukojć, A.; Grech, E.; Nowicka-Scheibe, J.

    2012-01-01

    In crystalline state 2,5-dichloro-3,6-dihydroxy-p-benzoquinone (chloranilic acid, CLA) forms with 4,4'-di-t-butyl-2,2'-bipyridyl (dtBBP) the hydrogen bonded chains along the b-axis. From one side of the CLA molecule the proton transfer takes place and the hydrogen bond length is very short (2.615 Å). A continuous infrared absorption is observed for dtBBP·CLA in the wavenumber range between 3100 and 800 cm -1 also indicating the strong hydrogen bonds. The DSC measurements show a weak, close to continuous, phase transition at 414 K. The complex dielectric permittivity for a single crystal sample was measured in the temperature range 100-440 K and at frequencies between 200 Hz and 2 MHz. The dielectric response is a combination of semiconducting properties and a relaxation process most probably connected with the proton dynamics in the hydrogen bonds. The mechanism of the structural phase transition is discussed.

  20. Photocatalytic degradation of Acephate, Omethoate, and Methyl parathion by Fe{sub 3}O{sub 4}@SiO{sub 2}@mTiO{sub 2} nanomicrospheres

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Lingling, E-mail: zllyslngj@126.com [State Key Laboratory of Food Science and Technology, School of Food Science of Jiangnan University, School of Food Science Synergetic Innovation Center of Food Safety and Quality Control, Wuxi, Jiangsu 214122 (China); Pi, Fuwei; Wang, Yifan [State Key Laboratory of Food Science and Technology, School of Food Science of Jiangnan University, School of Food Science Synergetic Innovation Center of Food Safety and Quality Control, Wuxi, Jiangsu 214122 (China); Xu, Hui [Key Laboratory of Healthy & Intelligent Kitchen System Integration, Ningbo, Zhejiang 315336 (China); Zhang, Yinzhi [State Key Laboratory of Food Science and Technology, School of Food Science of Jiangnan University, School of Food Science Synergetic Innovation Center of Food Safety and Quality Control, Wuxi, Jiangsu 214122 (China); Sun, Xiulan, E-mail: sxlzzz@jiangnan.edu.cn [State Key Laboratory of Food Science and Technology, School of Food Science of Jiangnan University, School of Food Science Synergetic Innovation Center of Food Safety and Quality Control, Wuxi, Jiangsu 214122 (China)

    2016-09-05

    Highlights: • An efficient photocatalyst Fe{sub 3}O{sub 4}@SiO{sub 2}@mTiO{sub 2} with high magnetic response and large specific surface area was synthesized. • Photocatalytic efficiency of Fe{sub 3}O{sub 4}@SiO{sub 2}@mTiO{sub 2} on Acephate, Omethoate, and Methyl Parathion was higher than TiO{sub 2} P-25. • Possible photocatalytic degradation mechanisms for the Acephate, Omethoate, and Methyl Parathion were proposed. - Abstract: A novel magnetic mesoporous nanomicrospheres Fe{sub 3}O{sub 4}@SiO{sub 2}@mTiO{sub 2} were synthetized and characterized by a series of techniques including FE-TEM, EDS, FE-SEM, PXRD, XPS, BET, TGA as well as VSM, and subsequently tested as a photocatalyst for the degradation of Acephate, Omethoate, and Methyl parathion under UV irradiation. The well-designed nanomicrospheres exhibit a pure and highly crystalline anatase TiO{sub 2} layer, large specific surface area, and high-magnetic-response. Photocatalytic degradation of the three organophosphorus pesticides (OPPs) and the formation intermediates were identified using HPLC, TOC-V{sub cpn}, IC, pH meter and GC–MS. Acephate, Omethoate, and Methyl parathion disappeared after 45 min, 45 min, and 80 min UV illumination, respectively. At the end of the treatment, the total organic carbon (TOC) of the OPPs was reduced 80–85%. The main mineralization products were SO{sub 4}{sup 2−}, NO{sub 3}{sup −} and PO{sub 4}{sup 3−} and Omethoate additionally formed NO{sub 2}{sup −}. Based on the results, we proposed the photocatalytic degradation pathways for Acephate, Omethoate, and Methyl parathion.

  1. CoFe2O4−Fe3O4 Magnetic Nanocomposites as Photocatalyst for the Degradation of Methyl Orange Dye

    Directory of Open Access Journals (Sweden)

    Debabrata Mishra

    2012-01-01

    Full Text Available We report the investigation of temperature-dependent magnetic properties and photocatalytic activity of CoFe2O4−Fe3O4 magnetic nanocomposites (MNCs synthesized by hydrothermal process. Room-temperature magnetic hysteresis (M-H loops result enhanced saturation magnetization of 90 emu/g and coercivity (HC of 530 Oe for CoFe2O4−Fe3O4 MNCs. With decreasing temperature to 20 K, HC increases from 500 Oe to 6800 Oe, and the M-H loops exhibit exchange coupling feature between CoFe2O4 and Fe3O4. Low- and high-temperature-dependent magnetization measurements confirm that the blocking temperature lies above 300 K and the presence of two magnetic phase transitions corresponding to CoFe2O4 and Fe3O4, respectively. The photocatalytic activity of the MNCs has been examined on the reduction of methyl orange (MO, a colored compound used in dyeing and printing textiles. The observed results suggest that the CoFe2O4−Fe3O4 MNCs act as an excellent photocatalyst on the degradation of organic contaminants and degrade 93% of MO in 5 hours of UV irradiation. The photocatalytic activity of MNCs is attributed to remarkably high band gap energy and small particle size. Also, the MNCs with a reproducible photocatalytic activity are well separable from water media by applying external magnetic field and acts as a promising catalyst for the remediation of textile wastewater.

  2. 树脂纳米零价铁催化过硫酸钠降解甲基橙的研究%Research on Degradation of Methyl Orange by Sodium Persulfate Activated with Resin Supported Nano Zero-valent Iron

    Institute of Scientific and Technical Information of China (English)

    崔广华; 程俊; 秦黎

    2012-01-01

      采用树脂负载零价纳米铁(NZVI-resin)作为铁源,活化过硫酸钠,产生硫酸根自由基氧化降解偶氮染料甲基橙.考察了温度、 NZVI-resin加入量、 pH值及过硫酸钠的浓度等因素对甲基橙降解率的影响,并对其降解动力学规律作了初步探讨.结果表明:降解反应遵循准一级反应动力学,在pH=3.0、 Fe0=0.2 g·L-1、 Na2S2O8=1.33 g·L-1的条件下,30 mg·L-1的甲基橙溶液降解率为99.7%.%  The article adopted the resin with nano zero-valent iron complex (NZVI-resin) as a source of iron to activate sodium persulfate and generate sulfate free radical which may oxidize degradation of methyl orange azo dye. The effects of temperature, the dosages of NZVI-resin, pH, the concentration of sodium persulfate on methyl orange degradation were also examined. In addition, its degradation kinetics was discussed. The results showed that the degradation of methyl orange followed the first order kinetics. And in the initial pH=3, Fe0=0.2 g·L-1, Na2S2O8=1.33 g·L-1, the degradation efficiency of methyl orange solution with a concentration of 30 mg·L-1could reach 99.7%.

  3. Influence of MnO2 on the photocatalytic activity of P-25 TiO2 in the degradation of methyl orange

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Influences of α-MnO2, β-MnO2, and δ-MnO2 on the photocatalytic activity of Degussa P-25 TiO2 have been investigated through the photocatalytic degradation of methyl orange. The TiO2 photocatalyst, before and after being contaminated by MnO2, was characterized by UV-visible diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). The results showed that photocatalytic activity of TiO2 could be inhibited significantly or completely deactivated due to the presence of even a small amount of MnO2 particles. It was found that the poisoning effect varied with the crystal phases of MnO2 and the effect was in the order δ-MnO2 >α-MnO2 >β-MnO2. The poisoning effect was attributed to the formation of heterojunctions between MnO2 and TiO2 particles. The heterojunctions changed the chemical state of Ti4+ and O2 sites in the crystalline phase of TiO2. MnO2 in contact with TiO2 particles also broadens the band-gap of TiO2, which decreases UV absorption of TiO2. It can also create some deep impurity energy levels serving as photoelec-tron-photohole recombination center, which accelerates the electron-hole recombination.

  4. Copper(II) coordination polymers: tunable structures and a different activation effect of hydrogen peroxide for the degradation of methyl orange under visible light irradiation.

    Science.gov (United States)

    Liu, Lu; Wu, Dongqing; Zhao, Bei; Han, Xiao; Wu, Jie; Hou, Hongwei; Fan, Yaoting

    2015-01-21

    By tuning the synthesis conditions, based on a conformation-sensitive ligand, 1,4-bis(1,2,4-triazole-1-methylene)-2,3,5,6-tetramethyl benzene (btmx) and Cu(NO3)2·3H2O/CuCl2·2H2O, we have obtained three Cu(ii) coordination polymers with diverse structures, namely, {[Cu(btmx)2(H2O)]·2NO3}n (), {[Cu(btmx)2(Cl)2]·5H2O}n () and [Cu(btmx)(Cl)2]n (). Complex exhibits a novel 2D → 3D interpenetrating structure with a point symbol of 6(3). Complex features an irregular 2D grid with (4(4)·6(2)) topology. The structure of complex is a 1D double chain structure. The ultraviolet-visible absorption spectra and TG curves of these complexes are also presented and discussed. Moreover, under visible light, the coordination polymers , , and display a different activation effect of hydrogen peroxide (H2O2) for the photocatalytic decomposition of methyl orange (MO), which indicates that the coordination polymers may have bright prospects in the field of photocatalytic degradation of dyes.

  5. Hydrothermal fabrication and visible-light-driven photocatalytic properties of bismuth vanadate with multiple morphologies and/or porous structures for methyl orange degradation.

    Science.gov (United States)

    Jiang, Haiyan; Dai, Hongxing; Meng, Xue; Zhang, Lei; Deng, Jiguang; Liu, Yuxi; Au, Chak Tong

    2012-01-01

    Monoclinic BiVO4 with multiple morphologies and/or porous structures were fabricated using the hydrothermal strategy. The materials were characterized by means of the XRD, Raman, TGA/DSC, SEM, XPS, and UV-Vis techniques. The photocatalytic activities of the BiVO4 materials were evaluated for the degradation of Methyl Orange under visible-light irradiation. It is observed that pH value and surfactant exerted a great effect on the morphology and pore structure of the BiVO4 product. Spherical BiVO4 with porous structures, flower-cluster-like BiVO4, and flower-bundle-like BiVO4 were generated hydrothermally at 100 degrees C with poly(vinyl pyrrolidone) (PVP) and urea (pH = 2) and at 160 degrees C with NaHCO3 (pH = 7 and 8), respectively. The PVP-derived BiVO4 showed much higher surface areas (5.0-8.4 m2/g) and narrower bandgap energies (2.45-2.49 eV). The best photocatalytic performance of the spherical BiVO4 material with a surface area of 8.4 m2/g was associated with its higher surface area, narrower bandgap energy, higher surface oxygen vacancy density, and unique porous architecture.

  6. Hydrothermal fabrication and visible-light-driven photocatalytic properties of bismuth vanadate with multiple morphologies and/or porous structures for Methyl Orange degradation

    Institute of Scientific and Technical Information of China (English)

    Haiyan Jiang; Hongxing Dai; Xue Meng; Lei Zhang; Jiguang Deng; Yuxi Liu; Chak Tong Au

    2012-01-01

    Monoclinic BiVO4 with multiple morphologies and/or porous structures were fabricated using the hydrothermal strategy.The materials were characterized by means of the XRD,Raman,TGA/DSC,SEM,XPS,and UV-Vis techniques.The photocatalytic activities of the BiVO4 materials were evaluated for the degradation of Methyl Orange under visible-light irradiation.It is observed that pH value and surfactant exerted a great effect on the morphology and pore structure of the BiVO4 product.Spherical BiV04 with porous structures,flower-cluster-like BiVO4,and flower-bundle-like BiVO4 were generated hydrothermally at lOO℃ with poly(vinyl pyrrolidone)(PVP)and urea(pH =2)and at 1600C with NaHCO3(pH =7 and 8),respectively.The PVP-derived BiVO4 showed much higher surface areas (5.0-8.4 m2/g)and narrower bandgap energies(2.45-2.49 eV).The best photocatalytic performance of the spherical BiVO4 material with a surface area of 8.4 m2/g was associated with its higher surface area,narrower bandgap energy,higher surface oxygen vacancy density,and unique porous architecture.

  7. Hierarchical structures constructed by BiOX (X = Cl, I) nanosheets on CNTs/carbon composite fibers for improved photocatalytic degradation of methyl orange

    Energy Technology Data Exchange (ETDEWEB)

    Weng, Baicheng, E-mail: baichengweng@gmail.com; Xu, Fenghua; Xu, Jianguang [Yancheng Institute of Technology, Materials Engineering Department (China)

    2014-12-15

    A hierarchical structure (CNTs/CFs-NSs) of BiOX (X = Cl, I) nanosheets (NSs) on carbon fibers (CFs) embedded with aligned carbon nanotubes (CNTs) with improved photocatalytic activities has been developed on a large scale. In the CNTs/CFs obtained by centrifugal spinning, CNTs align along the axis of the CFs, form π–π stacking interactions with CFs and strength the electrical conductivity of CFs, which favors the electron collection and transportation. Cross-flake BiOX NSs were uniformly grown on the surface of CNTs/CFs through a successive ionic layer adsorption and reaction process. The as-prepared BiOX NSs are less than 20 nm in thickness with dominant reactive (001) facets that are almost fully exposed, promoting the photocatalytic properties. The hierarchical CNTs/CFs-NSs show 3- and 2-fold improved photocatalytic activities for degradation of methyl orange for BiOCl and BiOI compared to corresponding neat NSs, respectively, given the synergistic effects of CNTs/CFs and NSs. Moreover, these novel hierarchical structures with stable performance enhance the recycled ability for the photocatalyst.

  8. Assessment of the UV/Cl2 advanced oxidation process for the degradation of the emerging contaminants amitriptyline hydrochloride, methyl salicylate and 2-phenoxyethanol in water systems.

    Science.gov (United States)

    Javier Benitez, F; Real, Francisco J; Acero, Juan L; Casas, Francisco

    2016-12-26

    Three emerging contaminants (amitriptyline hydrochloride (AH), methyl salicylate (MS) and 2-phenoxyethanol (PE)) frequently found in wastewaters were selected to be individually degraded in ultra-pure water by the advanced oxidation process (AOP) constituted by the combination of UV radiation and chlorine. The influence of pH, initial chlorine concentration and nature of the contaminants was firstly explored. The trend for the reactivity of the selected compounds was deduced: AH > MS > PE. A later kinetic study was carried out focused on the evaluation of the first-order rate constants and the determination of the partial contribution to the global reaction of the direct photochemical pathway and the radical pathway. In a second stage, the simultaneous oxidation of mixtures of the selected contaminants in several types of water was also performed by the same combination UV/Cl2. The efficiency of this combined system UV/Cl2 was compared to other oxidants such as the UV/[Formula: see text] and UV/H2O2 AOPs, and the influence of the operating variables was discussed. Results confirmed that the UV/Cl2 system provides higher elimination efficiencies among the AOPs tested. The presence of dissolved organic matter and bicarbonate ions in the water matrix caused a decrease in the treatment efficiency.

  9. CCDC 1024818: Experimental Crystal Structure Determination : 5-(((t-Butyl(dimethyl)silyl)oxy)(diphenyl)methyl)-2-phenyl-2,5,6,7-tetrahydro-3H-pyrrolo[2,1-c][1,2,4]triazole-3-selenone

    KAUST Repository

    Vummaleti, Sai V. C.

    2015-01-01

    An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

  10. Investigation into Degradation Property of Methyl Orange Solution by Fe-based Amorphous Powder%铁基非晶粉末对甲基橙溶液降解性能的影响

    Institute of Scientific and Technical Information of China (English)

    袁亚东; 彭程; 李维火; 方斌

    2016-01-01

    对铁基非晶粉末(Fe73.5Si13.5B9Nb3Cu1)进行等温退火和球磨处理,获得球磨的非晶粉末和球磨的退火非晶粉末。分析铁粉和3种非晶粉末对甲基橙溶液的降解率,研究铁基非晶粉末降解甲基橙溶液的能力,考察温度、溶液初始pH值、粉末投加量对铁基非晶粉末降解甲基橙溶液的影响。结果表明:与铁粉、球磨的非晶粉末和球磨的退火非晶粉末相比,铁基非晶粉末对甲基橙溶液的降解效果更好,质量浓度为10 mg/L的甲基橙溶液的降解率在23 h内可达97%;温度升高、甲基橙溶液初始pH值降低均有利于提高铁基非晶粉末对甲基橙溶液的降解率;粉末投加量对铁基非晶粉末降解甲基橙溶液有较大影响,本实验最佳铁基非晶粉末投加量为0.30 g(4.29 mg/mL),当粉末投加量增加为0.70 g(10 mg/mL)时,降解率下降。%Ball-milled amorphous powder and ball-milled annealed amorphous powder were obtained from Fe73.5Si13.5B9Nb3Cu1 amorphous powder, which were treated by isothermal anneal and ball milling. Comparing the degradation rates of iron powder and the 3 kinds of amorphous powder to methyl orange solution, the degradation property of methyl orange solution by Fe-based amorphous powder (Fe73.5Si13.5B9Nb3Cu1) was studied, and the effects of reaction temperature, initial pH value of methyl orange solution and powder dosage on methyl orange solution by Fe-based amorphous powder were also investigated. The results indicate that the Fe-based amorphous powder performs better on the degradation of methyl orange solution compared with iron powder, ball-milled amorphous powder and ball-milled annealed amorphous powder, which can degrade 10 mg/L methyl orange solution near 97% within 23 h; higher temperature and lower pH value of methyl orange solution lead to the increase of degradation efficiency of methyl orange solution. The amount of Fe-based amorphous powder has a significant influence on

  11. Photocatalytic Degradation of Methyl Orange on ZnCr Layered Double Hydroxides%锌铬水滑石可见光降解甲基橙的性能研究

    Institute of Scientific and Technical Information of China (English)

    薛源明; 樊丽辉; 刘东斌; 李士凤; 申延明

    2015-01-01

    采用共沉淀法制备n( Zn)/n( Cr)为2的ZnCr水滑石,采用X射线粉末衍射仪( XRD)、紫外-可见漫反射光谱仪( UV-Vis)等方法对催化剂的结构和性质进行表征.通过可见光下对甲基橙的催化降解表征催化剂的活性.结果表明:制备的样品具有水滑石的结构,对可见光具有吸收性能. ZnCr水滑石具有良好的催化降解甲基橙性能,适宜的降解条件是甲基橙初始质量浓度不超过80 mg/L,催化剂用量为1 g/L,此条件下光照180 min后甲基橙的降解率达到了93. 58 %.动力学研究表明:该催化降解过程在甲基橙质量浓度低(≤20 mg/L)的条件下符合1级反应动力学模型,而在甲基橙质量浓度高(≥40 mg/L)的条件下符合0. 5级反应动力学模型.%ZnCr Layered double hydroxides with n(Zn)/n(Cr) molar ratio of 2 was synthesized by the coprecipitation method. The photocatalyst was characterized by powder X-ray diffraction( XRD) and ul-traviolet-visible absorption spectroscopy ( UV-Vis ) . The photocatalyst was evaluated by photocatalytic degradation of methyl orange under visible-light irradiation. The results showed that the prepared sample had a layered double hydroxides structure and visible-light absorption ability. ZnCr layered double hydrox-ides had better performance in degradation of methyl orange. The suitable condition for degradation was the concentration of methyl orange was not more than 80 mg/L,and the amount of photocatalyst was 1. 0 g/L. The methyl orange degradation of 93. 58 % could be obtained after the irradiation of 180 min at the above condition. The kinetic results indicated that the degradation process followed first-order kinetics at lower methyl orange concentration(≤20 mg/L) ,and half order kinetics at higher methyl orange concen-tration(≥40 mg/L) .

  12. 利用电催化氧化技术降解甲基橙染料废水的研究%Study on Degradation of Methyl Orange Dye Wastewater by Electro-catalytic Oxidation Technology

    Institute of Scientific and Technical Information of China (English)

    马南; 王哲; 陈静

    2011-01-01

    [目的]研究电催化氧化技术降解甲基橙染料废水的工艺条件.[方法]以甲基橙为目标污染物,自制DSA电极和电催化反应装置,通过控制电极类型、电解质、电压和初始pH,比较分析甲基橙的去除效率.[结果]DSA电极比普通电极对甲基橙的去除率高;电压的增加和电解质的加入促进了电化学降解效率的提高;酸性条件下,DSA电极能够表现出对甲基橙较高的去除率.[结果]该研究为电催化氧化技术降解其他偶氮化合物提供技术依据.%[Objective] The research aimed to study the technological condition of methyl orange dye wastewater degradation by using the electro-catalytic oxidation technology. [Method] Methyl orange was theObjective pollutant. DSA electrode and electro-catalytic reaction equipment were self-made. By controlling electrode type, electrolyte, voltage and initial pH, the removal efficiency of methyl orange was contrasted and analyzed. [ Result] The removal efficiency of DSA electrode on methyl orange was higher than that of common electrode. The increase of voltage and addition of electrolyte promoted the improvement of electrochemical degradation efficiency. Under the acid condition, DSA electrode had high removal efficiency on methyl orange. [ Conclusion] The research provided the technology basis for degrading other azocompound by the electro-catalytic oxidation technology.

  13. The Nrf1 CNC/bZIP protein is a nuclear envelope-bound transcription factor that is activated by t-butyl hydroquinone but not by endoplasmic reticulum stressors.

    Science.gov (United States)

    Zhang, Yiguo; Lucocq, John M; Hayes, John D

    2009-03-01

    In rat liver RL-34 cells, endogenous Nrf1 (nuclear factor-erythroid 2 p45 subunit-related factor 1) is localized in the ER (endoplasmic reticulum) where it exists as a glycosylated protein. Electron microscopy has demonstrated that ectopic Nrf1 in COS-1 cells is located in the ER and the NE (nuclear envelope). Subcellular fractionation, together with a membrane proteinase protection assay, revealed that Nrf1 is an integral membrane protein with both luminal and cytoplasmic domains. The N-terminal 65 residues of Nrf1 direct its integration into the ER and NE membranes and tether it to a Triton X-100-resistant membrane microdomain that is associated with lipid rafts. The activity of Nrf1 was increased by the electrophile tBHQ (t-butyl hydroquinone) probably through an N-terminal domain-dependent process. We found that the NST (Asn/Ser/Thr-rich) domain, along with AD1 (acidic domain 1), contributes positively to the transactivation activity of full-length Nrf1. Furthermore, the NST domain contains seven putative -Asn-Xaa-Ser/Thr- glycosylation sites and, when glycosylation was prevented by replacing all of the seven asparagine residues with either glutamine (Nrf1(1-7xN/Q)) or aspartic acid (Nrf1(1-7xN/D)), the former multiple point mutant possessed less activity than the wild-type factor, whereas the latter mutant exhibited substantially greater activity. Lastly, the ER stressors tunicamycin, thapsigargin and Brefeldin A were found to inhibit basal Nrf1 activity by approximately 25%, and almost completely prevented induction of Nrf1-mediated transactivation by tBHQ. Collectively, these results suggest that the activity of Nrf1 critically depends on its topology within the ER, and that this is modulated by redox stressors, as well as by its glycosylation status.

  14. Catabolism of methyl ter-butyl ether (MTBE): characterization of the enzymes of Mycobacterium austroafricanum IFP 2012 involved in MTBE degradation; Catabolisme du methyl tert-butyl ether (MTBE): caracterisation des enzymes impliquees dans la degradation du MTBE chez Mycobacterium austroafricanum IFP 2012

    Energy Technology Data Exchange (ETDEWEB)

    Lopes Ferreira, N.

    2005-11-15

    Methyl tert-butyl ether (MTBE) is added to gasoline to meet the octane index requirement. its solubility in water and its poor biodegradability made the use of MTBE a great environmental concern, particularly regarding aquifers. We previously isolated M austroafricanum IFP 2012 able to use MTBE as a sole source of carbon and energy and the MTBE pathway was partially characterized. In the present study, which aimed at isolating the genes involved in MTBE biodegradation in order to use them for estimation of MTBE biodegradation capacities in contaminated environment, we isolated a new M. austroafricanum strain, IFP 2015. A new degradation intermediate, the 2-methyl 1,2-propane-diol (2-M1,2-PD), the product of tert-butanol (TBA) oxidation, was identified. We also determined the enzymes induced during growth of M. austroafricanum IFP 2012 on MTBF. Then, using the tools of protein analysis and of molecular biology, we isolated and cloned the mpd genes cluster in the plasmid pCL4D. Heterologous expression of the recombinant plasmid in M smegmatis tmc2 155, showed the involvement of an 2-M1,2-PD dehydrogenase (MpdB) and a hydroxy-iso-butyr-aldehyde dehydrogenase (MpdC), encoded by mpdB and mpdC, respectively. Both enzymes were responsible for the conversion of 2-M 1,2-PD to hydroxy-isobutyric acid (HIBA). A further survey of different M austroafricanum strains, including IFP 2012, IFP 2015 and JOBS (ex-M vaccae) showed the link between the ability to grow on C{sub 2} to C{sub 16} n-alkanes and the MTBE and TBA degradation capacities. The alkB gene was partially sequenced in all these strains. Expression of alkB was demonstrated in M. austroafricanum IFP 2012 after growth on propane, hexane, hexadecane and TBA. Finally, we identified 2-propanol as the intermediate of HIBA degradation. The gene encoding the 2-propanol:p-N,N'-dimethyl-4-nitroso-aniline (NDMA) oxidoreductase was detected M austroafricanum IFP 2012. (author)

  15. Weathering and Chemical Degradation of Methyl Eugenol and Raspberry Ketone Solid Dispensers for Detection, Monitoring, and Male Annihilation of Bactrocera dorsalis and Bactrocera cucurbitae (Diptera: Tephritidae) in Hawaii.

    Science.gov (United States)

    Vargas, Roger I; Souder, Steven K; Nkomo, Eddie; Cook, Peter J; Mackey, Bruce; Stark, John D

    2015-08-01

    Solid male lure dispensers containing methyl eugenol (ME) and raspberry ketone (RK), or mixtures of the lures (ME + RK), and dimethyl dichloro-vinyl phosphate (DDVP) were evaluated in area-wide pest management bucket or Jackson traps in commercial papaya (Carica papaya L.) orchards where both oriental fruit fly, Bactrocera dorsalis (Hendel), and melon fly, Bactrocera cucurbitae (Coquillett), are pests. Captures of B. dorsalis with fresh wafers in Jackson and bucket traps were significantly higher on the basis of ME concentration (Mallet ME [56%] > Mallet MR [31.2%] > Mallet MC [23.1%]). Captures of B. cucurbitae with fresh wafers in Jackson and bucket traps were not different regardless of concentration of RK (Mallet BR [20.1%] = Mallet MR [18.3%] = Mallet MC [15.9%]). Captures of B. dorsalis with fresh wafers, compared with weathered wafers, were significantly different after week 12; captures of B. cucurbitae were not significantly different after 16 wk. Chemical analyses revealed presence of RK in dispensers in constant amounts throughout the 16-wk trial. Degradation of both ME and DDVP over time was predicted with a high level of confidence by nonlinear asymptotic exponential decay curves. Results provide supportive data to deploy solid ME and RK wafers (with DDVP) in fruit fly traps for detection programs, as is the current practice with solid TML dispensers placed in Jackson traps. Wafers with ME and RK might be used in place of two separate traps for detection of both ME and RK responding fruit flies and could potentially reduce cost of materials and labor by 50%.

  16. 聚吡咯-碳酸银复合物的制备及光催化降解甲基橙的研究%Study on Preparation of Polypyrrole-Silver Carbonate Composites and Photocatalytic Degradation of Methyl Orange

    Institute of Scientific and Technical Information of China (English)

    彭望明

    2015-01-01

    在超声波作用下以硝酸银和碳酸钠制备超细碳酸银粉末,在冰浴条件下采用吡咯的原位聚合法,以过硫酸铵为氧化剂,制备聚吡咯-碳酸银复合材料,并以IR及激光粒度仪对复合材料进行了表征.将复合材料作为催化剂,模拟自然光照射下降解甲基橙水溶液,当复合材料用量为0.4 g,甲基橙溶液的pH为6.0,温度为40℃,甲基橙初始浓度为10 mg/L,降解时间为2.5 h时,甲基橙的降解率最高可达98.43%.%Silver carbonate ultrafine powder was prepared with silver nitrate and sodium carbonate under the condition of ultrasonic dispersion ,and polypyrrole- silver carbonate composites were sythsized with ammonium persulfate as the oxidant in situ polymerization. The performance of the composites were detected with IR ,XRD and Laser Particle Size Analyzer. Methyl orange was degraded with the composites as the catalyst under simulated natural light. When the dosage of the composites was 0. 4 g ,the initial concentration of methyl orange solution was 10 mg/L ,the degradation time was 2. 5 h ,the pH value of methyl orange solution was 6. 0,and temperature was 40℃,the degradation rate of methyl orange was up to 98. 43%.

  17. Study on Photocatalysis in Methyl Orange Degradation Using TiO_2 with Haydite as Carrier%TiO2/陶粒光催化降解甲基橙研究

    Institute of Scientific and Technical Information of China (English)

    张雷; 向龙玲; 郝慧聪; 王德英

    2011-01-01

    This paper presents the results of the photocatalysis degradation of methyl orange by nanosized TiO2 with haydite as carrier.Catalysts were prepared by sol-sel method and sintered in electrical resistance furnace.The XRD,TG-DTA,FT-IR were also used to characterize the catalysts.With methyl orange as target degradation product,the photocatalysis capability of the catalysts and influencing factors of photocatalysis degradation were studied,such as,sintering temperature,catalyst dosage and initial pH value of methyl orange.The results indicate that when the initial concentration of methyl orange was 100 mg/L,the optimal condition was initial pH=3,sintering temperature 700℃ and catalyst dosage 30 mg/L.%采用溶胶-凝胶法制备了以陶粒为载体的新型、高光催化活性的复合光催化剂TiO2/陶粒,使用XRD、TG-DTA、FT-IR进行表征;以甲基橙为目标降解物,考察了焙烧温度、催化剂投加量、初始pH值等因素对甲基橙去除效果的影响。结果表明:甲基橙初始浓度为100 mg/L时,最佳降解条件是pH=3,焙烧温度700℃,催化剂投加量30 g/L。

  18. Degradation of kresoxim-methyl in soil: impact of varying moisture, organic matter, soil sterilization, soil type, light and atmospheric CO2 level.

    Science.gov (United States)

    Khandelwal, Ashish; Gupta, Suman; Gajbhiye, Vijay T; Varghese, Eldho

    2014-09-01

    In the present investigation, persistence of kresoxim-methyl (a broad spectrum strobilurin fungicide) was studied in two different soil types of India namely Inceptisol and Ultisol. Results revealed that kresoxim-methyl readily form acid metabolite in soil. Therefore, residues of kresoxim-methyl were quantified on the basis of parent molecule alone and sum total of kresoxim-methyl and its acid metabolite. Among the two soil types, kresoxim-methyl and total residues dissipated at a faster rate in Inceptisol (T1/2 0.9 and 33.8d) than in Ultisol (T1/2 1.5 and 43.6d). Faster dissipation of kresoxim-methyl and total residues was observed in submerged soil conditions (T1/2 0.5 and 5.2d) followed by field capacity (T1/2 0.9 and 33.8d) and air dry (T1/2 2.3 and 51.0d) conditions. Residues also dissipated faster in 5% sludge amended soil (T1/2 0.7 and 21.1d) and on Xenon-light exposure (T1/2 0.5 and 8.0d). Total residues of kresoxim-methyl dissipated at a faster rate under elevated CO2 condition (∼550μLL(-)(1)) than ambient condition (∼385μLL(-)(1)). The study suggests that kresoxim-methyl alone has low persistence in soil. Because of the slow dissipation of acid metabolite, the total residues (kresoxim-methyl+acid metabolite) persist for a longer period in soil. Statistical analysis using SAS 9.3 software and Duncan's Multiple Range Test (DMRT) revealed the significant effect of moisture regime, organic matter, microbial population, soil type, light exposure and atmospheric CO2 level on the dissipation of kresoxim-methyl from soil (at 95% confidence level p<0.0001). Copyright © 2014 Elsevier Ltd. All rights reserved.

  19. 噻吩磺隆降解菌Bacillus subtilis LXL-7的分离与应用%Isolation and Utilization of a Thifensulfuron-methyl-degrading Bacterium,Bacillus subtilis LXL-7

    Institute of Scientific and Technical Information of China (English)

    李晓楼

    2016-01-01

    A strain LXL-7 isolated from soil highly degrades thifensulfuron-methyl,and was identified asBacillus subtilis. The degradation rate by LXL-7 reached 99.6% in mineral salt medium of thifensulfuron-methyl(100 mg/L)after 72 h. The optimal pH value and temperature were 7.5 and 30-35℃. The strain tolerated well to thifensulfuron-methyl and salt,at least to 400 mg/L of thifensulfuron-methyl and 4.0% NaCl. In addition,adding strain LXL-7 in the commercial preparation for soil amendment,a new multiple-function microbial preparation was developed,and it had an additional new function of degrading thifensulfuron-methyl residue in soil except original functions. Therefore, the strain LXL-7 could be considered for bioremediation of thifensulfuron-methyl pollution and development of microbial preparation.%从土壤中分离到一株能高效降解噻吩磺隆的细菌LXL-7,经鉴定LXL-7为枯草芽孢杆菌(Bacillus subtilis)。在含100 mg/L噻吩磺隆的培养基中,菌株LXL-7降解噻吩磺隆的72 h降解率可达99.6%以上。菌株LXL-7的最适pH为7.5,适宜温度为30-35℃,该菌还对噻吩磺隆和盐有很好的耐受性,至少能耐受400 mg/L的噻吩磺隆和4.0%的NaCl。另外,还通过在商品化的土壤微生物改良剂中添加菌株LXL-7开发了多功能微生物制剂,新制剂除原有功能外还增加了降解噻吩磺隆的新功能,故认为菌株LXL-7能够被用于噻吩磺隆污染的处理以及相关微生物制剂的开发。

  20. INFLUENCING FACTORS OF PHOTOCATALYTIC DEGRADATION OF METHYL ORANGE BY NANOMETER TITANIUM DIOXIDE IN AQUEOUS SOLUTIONS%水溶液中纳米二氧化钛光催化降解甲基橙的影响因素

    Institute of Scientific and Technical Information of China (English)

    张建民; 孙秀果; 高礼雄; 高俊刚

    2007-01-01

    用沸腾回流直接水解法制备了粒径为25~35 nm纯锐钛矿型纳米二氧化钛(TiO2).用X射线衍射和透射电镜表征材料的结构与形貌.用该催化剂催化降解甲基橙,研究了催化剂用量、甲基橙的起始浓度、溶液pH值、光强度、溶液中添加金属离子的影响.结果表明:在较强紫外光照射下,当甲基橙的起始浓度为0.02 g/L,TiO2用量为1.0g/L,光催化效率最高.酸性条件有利于光催化降解甲基橙.掺加Fe3+或Zn2+的光催化效率显著增加.掺加Mn2+或Ca2对光催化活性没有影响.在紫外光区域(366 nm),样品对催化降解水溶液中甲基橙的活性较高.%Pure anatase phase titanium dioxide(TiO2) with 25-35 nm grain size was prepared by direct hydrolysis under boiling reflux conditions. The structure and morphology of the materials were characterized by X-ray diffraction and transmission electron microscope. This catalyst was used for the photocatalytic degradation of methyl orange. The effects of the catalyst loading, initial concentration of methyl orange, pH value, light intensity, and addition of metal ions in solution were investigated. Experimental results indicate that the photocatalytic efficiency is best when the initial concentration of the methyl orange is 0.02 g/L, the loading concentration of TiO2 is 1.0 g/L and the UV irradiation is at a higher light intensity. Acidic medium accelerated the photocatalytic degradation rate of methyl orange. The degradation rate increased considerably with the addition of Fe3+ or Zn2+. The effects of the addition of Mn2+ and Ca2+ on the photocatalytic activity were not notable. The specimen showed good photoactivity upon the degradation of the methyl orange in aqueous solution in the ultraviolet range (366 nm).

  1. Treatment on Methyl Orange-Containing Simulation Wastewater by Ce3+ Ion Homogenous Electro-Catalytic Degradation Process%Ce3+电催化降解甲基橙模拟废水的研究

    Institute of Scientific and Technical Information of China (English)

    刘咏; 邹文慧; 廖洋; 操飞; 赵仕林

    2011-01-01

    Experiment of electro-catalytic degradation for treatment of wastewater containing methyl orange was carried out with Ce3 + as catalyst. The kinetics of electro-catalytic degradation wastewater in the Ce3+ system was investigated. In order to probe the decoloring mechanism of Ce3+ to the electro-catalytic degradation of methyl orange, a diaphragmless cell and a diaphragm cell were both filled with the wastewater respectively, and then electrolyzed in different conditions (concluding the dosing method, dosing position of Ce3+ and stirring mode). The changes of cerium concentration, methyl orange concentration, the chemical oxygen demand (COD), and UV-vis spectral in the electrolysis process were determined and analyzed. The results showed that the degradation of methyl orange in the Ce3 + system accorded with firstorder kinetics. The electro-catalytic degradation reaction of Ce3+ to the decolorization of methyl orange mainly happened in the cathode. The Ce3+ in wastewater mainly reduced H2O2 to ·OH, which had strong oxidizability, and could attack the azo bonds in the methyl orange and oxidize Ce3 + to Ce4+. Then the Ce4+ , complexed with the chromophore of methyl orange, was resulting in the blue shift of its absorption peaks to achieve the decolourization.%对添加Ce3+的甲基橙模拟废水进行了电催化处理实验,考察了Ce3+电催化降解甲基橙的反应动力学;为探讨Ce3+电催化降解甲基橙的脱色机理,将废水分别置入有隔膜和无隔膜电解槽中,在不同的条件(Ce3+的投加方式、位置和搅拌方式)下进行电解,测定分析了废水在电解过程中铈含量、甲基橙浓度、COD及体系紫外-可见吸收光谱图的变化.实验结果表明,Ce3+对甲基橙的电催化反应符合一级反应动力学;Ce3+对甲基橙脱色的电催化反应主要发生在阴极;加入废水中的Ce3+主要是通过将电解生成的H2O2还原为具有强氧化性的·OH进攻甲基橙分子中的偶氮键和Ce3+

  2. 复频超声降解甲基橙废水的实验研究%Experimental study on the degradation of methyl orange wastewater by multi-frequency ultrasonic

    Institute of Scientific and Technical Information of China (English)

    闫正; 程琛; 李文昭; 蒋保刚; 刘志强

    2013-01-01

    以甲基橙模拟废水为研究对象,用正交实验考察了影响复频超声降解甲基橙的因素.结果表明,正交因子影响权重:复频超声功率>超声作用时间>甲基橙初始浓度.最佳工艺条件:复频超声功率为150 W,超声作用时间为90 min,甲基橙初始质量浓度为10 mg/L,在此条件下,溶液脱色率为89.6%;当pH=2时,脱色率可达98%;添加CaCl2,脱色率和COD去除率均超过96%.总之,降低pH,提高温度,添加CaC12均能显著提高复频超声降解甲基橙废水的效果.%Taking simulated methyl orange wastewater as the research object, the effects of the influencing factors of multi-frequency ultrasonic on the degradation of methyl orange are investigated by orthogonal tests. The results show that the influence weights of orthogonal factors are as follows;the power of multi-frequency ultrasonic>ultrasonic reaction time>initial concentration of methyl orange. Under the following optimum process conditions: multi-frequency ultrasonic power is 150 W,reaction time of multi-frequency ultrasonic 90 min,and initial concentration of methyl orange 10 mg/L,the decolorization rate of the solution is 89.6%. When pH=2,the decolorization rate can reach 98%. When CaC2 is added,both the decolorization rate and COD removing rate of methyl orange are over 96%. In short, the degradation effectiveness of methyl orange wastewater by multi-frequency ultrasonic can significantly be improved by reducing pH, raising temperature and adding CaCl2.

  3. THE THERMAL AND ABLATIVE DEGRADATION OF SOME EPOXY RESINS CURED WITH METHYL BICYCLO(2.2.1)HEPTENE-2,3-DICARBOXYLIC ANHYDRIDE (NMA).

    Science.gov (United States)

    ABLATION), (* EPOXY RESINS , (*PYROLYSIS, EPOXY RESINS ), CYCLOALKENES, ANHYDRIDES, CATALYSTS, ADDITIVES, CROSSLINKING(CHEMISTRY), REACTION KINETICS, DEGRADATION, AGING(MATERIALS), INFRARED SPECTRA, CHROMATOGRAPHIC ANALYSIS.

  4. 超声波/紫外法处理甲基橙废水的实验研究%Study on the Degradation of Methyl Orange Wastewater by Ultrasound/UV-light

    Institute of Scientific and Technical Information of China (English)

    唐抒圆; 裴雪; 李欣; 龙海蛟; 孙磊

    2016-01-01

    以甲基橙废水为研究对象,考查超声波/紫外法对甲基橙废水的处理效果,及其影响因素与最佳处理条件。结果表明:甲基橙废水的最适反应时间为100min,最佳pH为3-7;US/UV法对10mg/L的甲基橙的COD去除效率为78.4%,脱色率为89.2%;US/UV法适用于低浓度的甲基橙废水处理,对于浓度高于10mg/L的甲基橙废水,处理效果欠佳。%[Abstract]Taking methyl orange wastewater as the research object,study on the effect,factor and best conditions about the degradation of methyl orange wastewater by ultrasound/UV-light.The results show that:the best reaction time is 100min,pH is 3-7;initial concentration of methyl orange is 10 mg/L,the removal efficiency of COD is 78.4%,the decolorization rate of the solution is 89.2%;US/UV is suitable for low concentration methyl orange wastewater,less effective when the initial concentration of methyl orange is more than 10 mg/L.

  5. Efecto del enriquecimiento con nutrientes en la degradación de clorpirifos, malatión y metil paratión Inorganic nutrients effect addition over the chlorpyrifos, malathion and methyl parathion degradation

    Directory of Open Access Journals (Sweden)

    S. A. Upegui

    2011-01-01

    Full Text Available Con el fin de evaluar el efecto del enriquecimiento con nutrientes (una sal de fósforo o un fertilizante comercial con N, P y K como alternativa para mejorar la capacidad de degradación de los microorganismos en una matriz sólida, contaminada con los pesticidas organofosforados: clorpirifos, malatión y metil paratión, se realizaron experimentos de cultivo bajo condiciones controladas de oscuridad, temperatura y humedad por 30 días. En todos los tratamientos hubo degradación de los pesticidas; sin embargo, en el tratamiento con fósforo los tiempos para degradar el clorpirifos y el metil paratión fueron mayores. La presencia de los pesticidas no generó efectos tóxicos detectables sobre la microflora en ninguno de los tratamientos evaluados. La actividad biológica de las matrices no presentó una relación directa con la capacidad de degradación.In order to evaluate the effect of inorganic nutrient addition (phosphorus or commercial fertilizer over the microbial degradation capacity present in a solid matrix contaminated with chlorpyrifos, malathion and methyl parathion, microcosms assays were held under controlled conditions of light, moisture and temperature for 30 days. Results showed that even though three treatments microorganisms were able to degrade the three organophosphorus pesticides, microorganisms of phosphorus-enrichment treatment were less efficient to degrade Chlorpyrifos and Methyl Parathion than microorganisms of Fertilizer-enrichment treatment. It was not observed a direct relation between mineralization and microbial pesticides degradation capacity. The microbial activity was not affected by the presence of organophosphorus pesticides.

  6. Photocatalytic degradation of methyl orange, methylene blue and rhodamine B with AgCl nanocatalyst synthesised from its bulk material in the ionic liquid [P6 6 6 14]Cl.

    Science.gov (United States)

    Rodríguez-Cabo, Borja; Rodríguez-Palmeiro, Iago; Corchero, Raquel; Rodil, Rosario; Rodil, Eva; Arce, Alberto; Soto, Ana

    2017-01-01

    The photocatalytic degradation of wastewater containing three industrial dyes belonging to different families, methyl orange (MO), methylene blue (MB) and Rhodamine B (RhB), was studied under UV-Vis irradiation using synthesised silver chloride nanoparticles. The nanocatalyst was prepared by a dissolution/reprecipitation method starting from the bulk powder and the ionic liquid trihexyl(tetradecyl)phosphonium chloride, [P6 6 6 14]Cl, without addition of other solvents. The obtained catalyst was characterised by UV-Vis absorbance, X-ray powder diffraction, transmission electron microscopy and scanning electron microscopy. The decolourisation of the samples was studied by UV-Vis absorbance at the corresponding wavelength. Starting from 10 ppm dye solutions and 1 g L(-1) of the synthesised AgCl nanoparticles, degradation efficiencies of 98.4% for MO, 98.6% for MB and 99.9% for RhB, were achieved in 1 h. The degradation mechanisms for the different dyes were studied. Comparison with other frequently used nanocatalysts, namely P-25 Degussa, TiO2 anatase, Ag and ZnO, highlights the strong catalytic activity of AgCl nanoparticles. Under the same experimental conditions, these nanoparticles led to higher (more than 10%) and faster degradations.

  7. Sb掺杂TiO2光催化降解甲基橙反应研究%Photo Catalysis Degradation of Methyl Orange over Sb Doped TiO2

    Institute of Scientific and Technical Information of China (English)

    黄文琼; 刘芳霞; 褚丽娟; 滕丹妮; 诸葛艳; 张雅; 宋丽; 赵松林

    2011-01-01

    The degradation of methyl orange (MO) catalyzed by Sb doped TiO2 catalyst under UV-light was conducted. Catalyst preparing and catalysis degradation conditions such as Sb contenting in TiO2, calcining temperature and time,catalyst amount, H2O2 dosage, reaction time, light conditions effecting on the degradation ratio of MO has been investigated. The results show that, 5wt% Sb contenting in TiO2 showed good catalytic activity. Under optimum conditions, degradation ratio of MO can be up to 100% in 240 min.%考察了Sb参杂TiO2催化剂光催化降解甲基橙(MO)反应性能.研究了催化剂制备条件、Sb负载量、催化剂用量、H2 O2用量、反应时间、光照等实验条件对MO降解率的影响.实验结果表明,Sb负载量为5%的TiO2表现出了良好的催化活性.在优化条件下,反应240 min可将浓度为100 mg/L的MO完全降解.

  8. Use of a hand-portable gas chromatograph-toroidal ion trap mass spectrometer for self-chemical ionization identification of degradation products related to O-ethyl S-(2-diisopropylaminoethyl) methyl phosphonothiolate (VX).

    Science.gov (United States)

    Smith, Philip A; Lepage, Carmela R Jackson; Savage, Paul B; Bowerbank, Christopher R; Lee, Edgar D; Lukacs, Michael J

    2011-04-01

    The chemical warfare agent O-ethyl S-(2-diisopropylaminoethyl) methyl phosphonothiolate (VX) and many related degradation products produce poorly diagnostic electron ionization (EI) mass spectra by transmission quadrupole mass spectrometry. Thus, chemical ionization (CI) is often used for these analytes. In this work, pseudomolecular ([M+H](+)) ion formation from self-chemical ionization (self-CI) was examined for four VX degradation products containing the diisopropylamine functional group. A person-portable toroidal ion trap mass spectrometer with a gas chromatographic inlet was used with EI, and both fixed-duration and feedback-controlled ionization time. With feedback-controlled ionization, ion cooling (reaction) times and ion formation target values were varied. Evidence for protonation of analytes was observed under all conditions, except for the largest analyte, bis(diisopropylaminoethyl)disulfide which yielded [M+H](+) ions only with increased fixed ionization or ion cooling times. Analysis of triethylamine-d(15) provided evidence that [M+H](+) production was likely due to self-CI. Analysis of a degraded VX sample where lengthened ion storage and feedback-controlled ionization time were used resulted in detection of [M+H](+) ions for VX and several relevant degradation products. Dimer ions were also observed for two phosphonate compounds detected in this sample.

  9. Study on photocatalytic degradation of methyl orange with modification of silver doped titania%改性掺银二氧化钛对甲基橙的光催化降解研究

    Institute of Scientific and Technical Information of China (English)

    吴静; 钱晓荣; 郁桂云

    2012-01-01

    采用钛酸四丁酯为主要原料,以溶胶-凝胶法制备TiO2及不同Ag含量的Ag-TiO2,通过X射线衍射仪及傅里叶红外光谱仪对其结构进行必要的表征.以高压汞灯为光源,研究了TiO2及Ag-TiO2对甲基橙的光催化降解情况.结果表明,掺杂Ag+的TiO2对甲基橙的光催化降解效果较好.%In this paper four butyl titanate is main raw material, prepared TiO2 and different Ag contents of the Ag-TiO2 by sol-gel method. By using X ray diffraction and Fu Liye infrared spectrometer its structure was characterized. Using a high pressure mercury lamp as light source,the initial concentration of methyl orange was degradated. The result indicated that the Ag+ doped TiO2 for methyl orange photocatalytic deg-radation effect is better than TiO2.

  10. Hydrothermal synthesis of TiO2 nanorod and Their Applicationinphotocatalytic Degradation of Methyl Orange%水热合成TiO2纳米棒及其光催化降解甲基橙研究

    Institute of Scientific and Technical Information of China (English)

    李家贵; 韦庆敏; 刘国聪

    2013-01-01

      The TiO2 nanorod photocatalysts was prepared by Hydrothermal synthesis with the materials of titanium dioxide powder,and the morphology of TiO2 nanorod was characterized by mean of XRD and TEM technique.Methyl orange were used to simulate dye wastewater.The effect factors of the amount of TiO2 nanorod,inatial concentration of Methyl orange,pH value of solution,reation time were studied with TiO2 nanorod as catalyst under ultraviolet light. The experimental results show that there is an optimal catalyst dossge of 0.2g/L;inatial concentration of Methyl orang of 10mg/L,pH=5~6;the degradation rate of Methyl orange reached to 96.5%under ultraviolet light irradiation after 3h;TiO2 nanorod photocatalyst after 5 times reuse and the degradation rate of Methyl orange is 85.6%.%  以锐钛矿TiO2粉末为原料,采用水热法合成了Ti02纳米棒,并利用X射线粉末衍射仪(XRD)、透射电子显微镜TEM等手段对产品进行了表征.以甲基橙为模拟染料废水,TiO2纳米棒为催化剂,在紫外光照条件下考察TiO2纳米棒的投加量、甲基橙的初始浓度、光照时间、溶液pH值及重复使用次数对甲基橙光降解效率的影响。实验结果表明:TiO2纳米棒的投加质量浓度为0.2g/L,甲基橙初始浓度为10mg/L,pH为5~6;光催化反应3h后,甲基橙的降解率可达96.5%;TiO2纳米棒重复使用5次后,甲基橙的降解率仍然可达85.6%.

  11. Weathering and chemical degradation of methyl eugenol and raspberry ketone solid dispensers for detection, monitoring and male annihilation of Bactrocera dorsalis and Bactrocera cucurbitae (Diptera: Tephritidae) in Hawaii

    Science.gov (United States)

    Solid male lure dispensers containing methyl eugenol (ME) and raspberry ketone (RK), or mixtures of the lures (ME + RK), and dimethyl dichloro-vinyl phosphate (DDVP) were evaluated in AWPM bucket or Jackson traps in commercial papaya (Carica papaya L.) orchards where both oriental fruit fly, Bactroc...

  12. Metabolic pathway involved in 2-methyl-6-ethylaniline degradation by Sphingobium sp. strain MEA3-1 and cloning of the novel flavin-dependent monooxygenase system meaBA.

    Science.gov (United States)

    Dong, Weiliang; Chen, Qiongzhen; Hou, Ying; Li, Shuhuan; Zhuang, Kai; Huang, Fei; Zhou, Jie; Li, Zhoukun; Wang, Jue; Fu, Lei; Zhang, Zhengguang; Huang, Yan; Wang, Fei; Cui, Zhongli

    2015-12-01

    2-Methyl-6-ethylaniline (MEA) is the main microbial degradation intermediate of the chloroacetanilide herbicides acetochlor and metolachlor. Sphingobium sp. strain MEA3-1 can utilize MEA and various alkyl-substituted aniline and phenol compounds as sole carbon and energy sources for growth. We isolated the mutant strain MEA3-1Mut, which converts MEA only to 2-methyl-6-ethyl-hydroquinone (MEHQ) and 2-methyl-6-ethyl-benzoquinone (MEBQ). MEA may be oxidized by the P450 monooxygenase system to 4-hydroxy-2-methyl-6-ethylaniline (4-OH-MEA), which can be hydrolytically spontaneously deaminated to MEBQ or MEHQ. The MEA microbial metabolic pathway was reconstituted based on the substrate spectra and identification of the intermediate metabolites in both the wild-type and mutant strains. Plasmidome sequencing indicated that both strains harbored 7 plasmids with sizes ranging from 6,108 bp to 287,745 bp. Among the 7 plasmids, 6 were identical, and pMEA02' in strain MEA3-1Mut lost a 37,000-bp fragment compared to pMEA02 in strain MEA3-1. Two-dimensional electrophoresis (2-DE) and protein mass fingerprinting (PMF) showed that MEA3-1Mut lost the two-component flavin-dependent monooxygenase (TC-FDM) MeaBA, which was encoded by a gene in the lost fragment of pMEA02. MeaA shared 22% to 25% amino acid sequence identity with oxygenase components of some TC-FDMs, whereas MeaB showed no sequence identity with the reductase components of those TC-FDMs. Complementation with meaBA in MEA3-1Mut and heterologous expression in Pseudomonas putida strain KT2440 resulted in the production of an active MEHQ monooxygenase.

  13. Simultaneous determination of methyl tert.-butyl ether and its degradation products, other gasoline oxygenates and benzene, toluene, ethylbenzene and xylenes in Catalonian groundwater by purge-and-trap-gas chromatography-mass spectrometry.

    Science.gov (United States)

    Rosell, Mònica; Lacorte, Sílvia; Ginebreda, Antoni; Barceló, Damià

    2003-05-02

    In Catalonia (northeast Spain), a monitoring program was carried out to determine methyl tert.-butyl ether (MTBE), its main degradation products, tert.-butyl alcohol (TBA), tert.-butyl formate (TBF), and other gasoline additives, the oxygenate dialkyl ethers ethyl tert.-butyl ether, tert.-amyl methyl ether and diisopropyl ether and the aromatic compounds benzene, toluene, ethylbenzene and xylene (BTEX) in 21 groundwater wells that were located near different gasoline point sources (a gasoline spill and underground storage tank leakage). Purge-and-trap coupled to gas chromatography-mass spectrometry was optimised for the simultaneous determination of the above mentioned compounds and enabled to detect concentrations at ng/l or sub-microg/l concentrations. Special attention was given to the determination of polar MTBE degradation products, TBA and TBF, since not much data on method performance and environmental levels are given on these compounds in groundwater. All samples analysed contained MTBE at levels between 0.3 and 70 microg/l. Seven contaminated hot spots were identified with levels up to US Environmental Protection Agency drinking water advisory (20-40 microg/l) and a maximum concentration of 670 microg/l (doubling the Danish suggested toxicity level of 350 microg/l). Samples with high levels of MTBE contained 0.1-60 microg/l of TBA, indicating (but not proving) in situ degradation of parent compound. In all cases, BTEX was at low concentrations or not detected showing less solubility and persistence than MTBE. This fact confirms the suitability of MTBE as a tracer or indicator of long-term gasoline contamination than the historically used BTEX.

  14. DNA methylation at the C-5 position of cytosine by methyl radicals: a possible role for epigenetic change during carcinogenesis by environmental agents.

    Science.gov (United States)

    Kasai, Hiroshi; Kawai, Kazuaki

    2009-06-01

    During carcinogenesis, methylation of the C-5 position of cytosines in the promoter region of tumor suppressor genes is often observed. Enzymatic DNA methylation is a widely accepted mechanism for this phenomenon. It is interesting to propose a free radical mechanism for 5-methyldeoxycytidine (m(5)dC) production, because the C-5 position of cytosine is an active site for free radical reactions. When deoxycytidine (dC) and cumene hydroperoxide (CuOOH), a tumor promoter and a methyl radical producer, were reacted in the presence of ferrous ion at pH 7.4, the formation of m(5)dC was observed. The same reaction also proceeded with t-butyl hydroperoxide (BuOOH). The formation of m(5)dC was also observed in DNA by the CuOOH treatment. This is the first report of chemical DNA methylation at cytosine C-5 by environmental tumor promoters. We propose here that this reaction is one of the important mechanisms of de novo DNA methylation during carcinogenesis, because methyl radicals are produced by the biotransformation of various endogenous and exogenous compounds.

  15. Development and Validation of a Stability Indicating RP-HPLC Method for Hydrocortisone Acetate Active Ingredient, Propyl Parahydroxybenzoate and Methyl Parahydroxybenzoate Preservatives, Butylhydroxyanisole Antioxidant, and Their Degradation Products in a Rectal Gel Formulation.

    Science.gov (United States)

    Ascaso, Magda; Pérez-Lozano, Pilar; García, Mireia; García-Montoya, Encarna; Miñarro, Montse; Ticó, Josep R; Fàbregas, Anna; Carrillo, Carolina; Sarrate, Rocío; Suñé-Negre, Josep M

    2015-01-01

    A stability indicating method was established through a stress study, wherein different methods of degradation (oxidation, hydrolysis, photolysis, and temperature) were studied simultaneously to determine the active ingredient hydrocortisone acetate, preservatives propyl parahydroxybenzoate, and methyl parahydroxybenzoate, antioxidant butylhydroxyanisole (BHA), and their degradation products in a semisolid dosage gel form. The proposed method was suitably validated using a Zorbax SB-Phenyl column and gradient elution. The mobile phase consisted of a mixture of methanol, acetonitrile, and water in different proportions according to a planned program at a flow rate of 1.5 mL/min. The diode array detector was set at 240 nm for the active substance and two preservatives, and 290 nm for BHA. The validation study was conducted according to International Conference on Harmonization guidelines for specificity, linearity, repeatability, precision, and accuracy. The method was used for QC of hydrocortisone acetate gel and for the stability studies with the aim of quantifying the active substance, preservatives, antioxidant, and degradation products. It has proved to be suitable as a fast and reliable method for QC.

  16. Optical Properties of ZnO Nanotubes and Their Photocatalytic Activity for Degradation of Methyl Orange%ZnO纳米管的光学性质及其对甲基橙降解的光催化活性

    Institute of Scientific and Technical Information of China (English)

    李长全; 罗来涛; 熊光伟

    2009-01-01

    以十二烷基硫酸钠为模板剂采用水热法合成了ZnO纳米管,以尿素和ZnSO_4为原料制备了ZnO纳米颗粒,并应用透射电镜、x射线衍射、光致发射光谱、拉曼光谱、比表面积测定、傅里叶红外光谱和紫外-可见漫反射光谱等技术对样品进行了表征.结果表明,ZnO纳米管的比表面积较大,在λ≈650nm的可见光波段ZnO纳米管开始出现吸收峰,而ZnO纳米颗粒在可见光波段几乎没有吸收.ZnO纳米管和纳米颗粒在紫外光照射下均对甲基橙有降解作用,其中ZnO纳米管的光催化活性较高.随着催化剂用量的增加和光照时间的延长,甲基橙降解率逐渐提高;甲基橙浓度的增大使甲基橙降解率降低.%ZnO nanotubes were synthesized by the hydrothermal method using sodium dodecyl sulfate as the template, and ZnO nanopar-tides were prepared with urea and ZnSO_4 as raw materials. The optical properties and photocatalytic activity of ZnO nanotubes and nanopar-ticles were studied, and the samples were characterized by transmission electron microscopy, X-ray diffraction, photoluminescence spec-troscopy, Raman spectroscopy, specific surface area determination, Fourier transform infrared spectroscopy, and ultraviolet-visual diffuse reflection spectroscopy. The ZnO nanotubes had larger specific surface area than the ZnO nanoparticles. The absorption peak of ZnO nanotubes began to appear atλ≈650 nm, but the ZnO nanoparticles nearly had no absorptive capacity in the visible band. ZnO nanotubes and nanoparticles can degradate methyl orange under ultraviolet light, and the catalytic activity of ZnO nanotubes was greater than that of ZnO nanoparticles. With the increase in the catalyst amount and illumination time, the degradation rate of methyl orange increased. Increasing the methyl orange concentration reduced the degradation rate.

  17. Cu2O/ZnO复合光催化剂的制备及对甲基蓝的降解%Preparation of Cu2O/ZnO composite photocatalyst and degradation of methyl blue

    Institute of Scientific and Technical Information of China (English)

    谷芳

    2013-01-01

    Cu2O was fixed by ZnO carrier,Cu2O/ZnO composite photocatalyst was prepared by dip-reduction-air oxidation process in this paper.Cu2O/ZnO composite photocatalyst had better light catalytic properties by controlling reactant ratio,drying temperature and drying time.The composite photocatalyst was used to degrade difficult degradation of acid dye methyl blue in the environment of the common.The influence factors of illumination time,catalyst dosing quantity,pH and initial concentration of solution were investigated.The results showed that the removal rate of methyl blue was 92% incandescent lamp irradiation 60 min.%以ZnO为载体,用其固定Cu2O,利用浸渍-还原-空气氧化法制备Cu2O/ZnO复合光催化剂.通过控制投料比、干燥温度和干燥时间等因素,得到了具有较好光催化性能的Cu2O/ZnO复合光催化剂.利用这种复合光催化剂对环境中常见的难降解的酸性染料甲基蓝进行降解,考察了光照时间、催化剂投加量、溶液pH值、溶液的初始质量浓度等因素对光催化性能的影响.结果表明,在白炽灯照射下反应60 min后,甲基蓝的去除率为92%.

  18. Single methyl group determines prion propagation and protein degradation activities of yeast heat shock protein (Hsp)-70 chaperones Ssa1p and Ssa2p.

    Science.gov (United States)

    Sharma, Deepak; Masison, Daniel C

    2011-08-16

    Organisms encode multiple homologous heat shock protein (Hsp)-70s, which are essential protein chaperones that play the major role in cellular protein "quality control." Although Hsp70s are functionally redundant and highly homologous, many possess distinct functions. A regulatory motif underlying such distinctions, however, is unknown. The 98% identical cytoplasmic Hsp70s Ssa1p and Ssa2p function differently with regard to propagation of yeast [URE3] prions and in the vacuolar-mediated degradation of gluconeogenesis enzymes, such as FBPase. Here, we show that the Hsp70 nucleotide binding domain (NBD) regulates these functional specificities. We find little difference in ATPase, protein refolding, and amyloid inhibiting activities of purified Ssa1p and Ssa2p, but show that interchanging NBD residue alanine 83 (Ssa1p) and glycine 83 (Ssa2p) switched functions of Ssa1p and Ssa2p in [URE3] propagation and FBPase degradation. Disrupting the degradation pathway did not affect prion propagation, however, indicating these are two distinct processes where Ssa1/2p chaperones function differently. Our results suggest that the primary evolutionary pressure for Hsp70 functional distinctions is not to specify interactions of Hsp70 with substrate, but to specify the regulation of this activity. Our data suggest a rationale for maintaining multiple Hsp70s and suggest that subtle differences among Hsp70s evolved to provide functional specificity without affecting overall enzymatic activity.

  19. Solar degradation of 5-amino-6-methyl-2-benzimidazolone by TiO{sub 2} and iron (III) catalyst with H{sub 2}O{sub 2} and O{sub 2} as electron acceptors

    Energy Technology Data Exchange (ETDEWEB)

    Sarria, V.; Peringer, P.; Pulgarin, C. [Swiss Federal Institute of Technology, Lausanne (Switzerland). Institute of Environmental Science and Technology, Laboratory for Environmental Biotechnology; Caceres, J.; Blanco, J.; Malato, S. [Plataforma Solar de Almeria, Tabernas (Spain)

    2004-05-01

    Wastewater containing mainly 5-amino-6-methyl-2-benzimidazolone (AMBI), used in the manufacture of dyes, was characterized as bio-recalcitrant by means of different biodegradability tests. In order to enhance the biodegradability of this important pollutant, solar photocatalytic degradation methods were explored. The systems light/TiO{sub 2}/O{sub 2}, light/TiO{sub 2}/H{sub 2}O{sub 2}, light/Fe{sup 3+}/O{sub 2} and lightFe{sup 3+}/H{sub 2}O{sub 2} were compared under direct sunlight at the Plataforma Solar de Almeria (Spain), using a Compound Parabolic Collector (CPC). The iron photo-assisted systems exhibited the most interesting behaviour, from the kinetic and engineering points of view, especially if their combination (as pre-treatment) with a biological process is considered. To compare the efficiency of these systems, the evolution of the following parameters were studied: (a) the dissolved organic carbon and initial compound concentration, (b) the toxicity, and (c) the biodegradability of treated solution. At lab scale, using a solar lamp, the degradation rate of the system light/Fe{sup 3+}/H{sub 2}O{sub 2} was two times higher than the system light/Fe{sup 3+}/O{sub 2} but this last system does not need H{sub 2}O{sub 2} addition, improving the economical requirements of the system. (author)

  20. Solar degradation of 5-amino-6-methyl-2-benzimidazolone by TiO{sub 2} and iron(III) catalyst with H{sub 2}O{sub 2} and O{sub 2} as electron acceptors

    Energy Technology Data Exchange (ETDEWEB)

    Sarria, Victor; Peringer, Paul; Caceres, Julia; Blanco, Julian; Malato, Sixto; Pulgarin, Cesar

    2004-05-01

    Wastewater containing mainly 5-amino-6-methyl-2-benzimidazolone (AMBI), used in the manufacture of dyes, was characterized as bio-recalcitrant by means of different biodegradability tests. In order to enhance the biodegradability of this important pollutant, solar photocatalytic degradation methods were explored. The systems light/TiO{sub 2}/O{sub 2}, light/TiO{sub 2}/H{sub 2}O{sub 2}, light/Fe{sup 3+}/O{sub 2} and light/Fe{sup 3+}/H{sub 2}O{sub 2} were compared under direct sunlight at the Plataforma Solar de Almeria (Spain), using a Compound Parabolic Collector (CPC). The iron photo-assisted systems exhibited the most interesting behaviour, from the kinetic and engineering points of view, especially if their combination (as pre-treatment) with a biological process is considered. To compare the efficiency of these systems, the evolution of the following parameters were studied: (a) the dissolved organic carbon and initial compound concentration, (b) the toxicity, and (c) the biodegradability of treated solution. At lab scale, using a solar lamp, the degradation rate of the system light/Fe{sup 3+}/H{sub 2}O{sub 2} was two times higher than the system light/Fe{sup 3+}/O{sub 2} but this last system does not need H{sub 2}O{sub 2} addition, improving the economical requirements of the system.

  1. Fabrication of highly active Melem/Zn0.25Cd0.75S composites for the degradation of bisphenol A and methyl orange under visible light irradiation

    Science.gov (United States)

    Wang, Xiaodong; Yan, Tao; Liu, Xiaohuan; Ji, Pengge; Sun, Meng; Wei, Dong; Yan, Liangguo; Du, Bin

    2016-11-01

    Metal-free polymeric catalyst hold great promise owing to their abundant sources, low-cost fabrication and easy processibility. Melem, an important intermediate during condensation of melamine rings to graphitic carbon nitride (g-C3N4), was synthesized by simple solid phase polymerization process. A novel Melem/Zn0.25Cd0.75S composite was fabricated through a facile one-step hydrothermal method. The as-products were characterized by X-ray diffraction (XRD), UV-vis DRS spectroscopy, fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM). The TEM and HRTEM results reveal that Zn0.25Cd0.75S nanoparticles and Melem closely contact with each other to form an intimate interface. The as-prepared composites exhibit significantly enhanced visible light photocatalytic performance for the degradation of Methyl orange (MO) and Bisphenol A (BPA), which could be attributed to the effective photo-induced charges transfer and separation in Melem/Zn0.25Cd0.75S composites. On the basis of radical scavenger experiments, superoxide radicals and holes are suggested to play a critical role in MO degradation over Melem/Zn0.25Cd0.75S heterojunctions. A possible mechanism for charge separation and transfer in the Melem/Zn0.25Cd0.75S composites was proposed to explain the enhanced photocatalytic performance.

  2. Unique cellular events occurring during the initial interaction of macrophages with matrix-retained or methylated aggregated low density lipoprotein (LDL). Prolonged cell-surface contact during which ldl-cholesteryl ester hydrolysis exceeds ldl protein degradation.

    Science.gov (United States)

    Buton, X; Mamdouh, Z; Ghosh, R; Du, H; Kuriakose, G; Beatini, N; Grabowski, G A; Maxfield, F R; Tabas, I

    1999-11-05

    A critical event in atherogenesis is the interaction of arterial wall macrophages with subendothelial lipoproteins. Although most studies have investigated this interaction by incubating cultured macrophages with monomeric lipoproteins dissolved in media, arterial wall macrophages encounter lipoproteins that are mostly bound to subendothelial extracellular matrix, and these lipoproteins are often aggregated or fused. Herein, we utilize a specialized cell-culture system to study the initial interaction of macrophages with aggregated low density lipoprotein (LDL) bound to extracellular matrix. The aggregated LDL remains extracellular for a relatively prolonged period of time and becomes lodged in invaginations in the surface of the macrophages. As expected, the degradation of the protein moiety of the LDL was very slow. Remarkably, however, hydrolysis of the cholesteryl ester (CE) moiety of the LDL was 3-7-fold higher than that of the protein moiety, in stark contrast to the situation with receptor-mediated endocytosis of acetyl-LDL. Similar results were obtained using another experimental system in which the degradation of aggregated LDL protein was delayed by LDL methylation rather than by retention on matrix. Additional experiments indicated the following properties of this interaction: (a) LDL-CE hydrolysis is catalyzed by lysosomal acid lipase; (b) neither scavenger receptors nor the LDL receptor appear necessary for the excess LDL-CE hydrolysis; and (c) LDL-CE hydrolysis in this system is resistant to cellular potassium depletion, which further distinguishes this process from receptor-mediated endocytosis. In summary, experimental systems specifically designed to mimic the in vivo interaction of arterial wall macrophages with subendothelial lipoproteins have demonstrated an initial period of prolonged cell-surface contact in which CE hydrolysis exceeds protein degradation.

  3. Isolation and Identification of Haloxyfop-R-methyl Degrading Bacteria%高效盖草能降解菌的分离与鉴定

    Institute of Scientific and Technical Information of China (English)

    张宇; 闫春秀; 王萌; 楚小强; 邓晓

    2011-01-01

    According to the potential carryover of long residual pesticide's residual to rotational crops,takingHaloxyfop-R-methyl as a model pollutant, three bacterial strains were isolated by selective enrichment from soil exposed to long residual herbicides, then the cultural characteristics and biochemical features of the three strains were determined and identified as HM1 ,HM2 and HM3,HM1 and HM2 were identified as Bacillus sp. , while HM3 was identified as Methyloeoccus sp. Then the effect of sugar content, temperature, pH value and initial concentration of haloxyfop-R-methyl on the growth of the three strains were studied,it was found out that the optimal sugar content for HM1 and HM3 was 0%,and HM2 was 0.5%; the optimal temperature range for HM3 and HM1 was 20 ℃ to 37 ℃ ,and HM2 was 25 ℃ to 41 ℃; the optimal range of pH for HM3 was 6.0 to 9.0 ,that for HM1 and HM2 was 6.0 to 8.0; the optimal initial concentration of Haloxyfop-R-methyl for HM3 was 200 mg/L,that for HM1 and HM2 was 100 mg/L.%针对海南地区长残效除草剂残留对后茬产生药害问题,以高效盖草能作为研究对象,采用富集培养的方法从长期施用长残效除草剂的土壤中分离到3株细菌,经过对这3株降解菌的培养特性及生理生化特征的测定试验,经传统鉴定方法对3种菌种进行鉴定,结果显示,HM1和HM2同为芽孢杆菌属(Bacillus sp.),HM3为甲基球菌属(Methyloeoccus sp.).并分别研究了培养含糖量、温度、pH和高效盖草能初始浓度对分离出的3株降解菌生长的影响,结果表明,HM1和HM3的最适含糖量是0.HM2的最适含糖量为0.5%;HM1和HM3的最适温度范围相同,为20~37℃,HM2的最造温度为25~41℃;HM1、HM2和HM3的最适生长温度分别是35、30和30℃;HM3的生长对酸碱度要求不严格,最适生长pH范围为6.0~9.0.HM1适宜在中性偏酸的条件下生长,而HM2则适宜在中性偏碱的条件下生长,其最适生长pH均为6.0~8.0;HM1和HM2生长的

  4. Photo catalytic degradation of organic dyes under solar irradiation: oxidation of Methyl-organe and orange II in aqueous suspension of titanium dioxide powder

    Energy Technology Data Exchange (ETDEWEB)

    Augugliaron, V.; Baiocchi, C.; Bianco Prevot, A.; Brussino, M. c.; Caceres Vazquez, J.; Garcia-Lopez, E.; Loddo, V.; Malato Rodriguez, S.; Marci, G.; Palmisano, L.; Pramauro, E.

    2001-07-01

    The photocatalytic oxidation of methyl-orange (C{sub 1}4H{sub 1}4N{sub 3}SO{sub 3}Na) and arange II (C{sub 1}6H{sub 1}1N{sub 2}SO{sub 4}Na) dyes was carried out in aqueous suspensions of polycrystalline TiO{sub 2} (anatase) irradiated by sunlight. The influence of th epresence of strong oxidant (H{sub 2}O{sub 2}S{sub 2}O{sub 8}''2) and ionic )Cl, SO{sub 4}''2) species on the process was studied. The dependende of dye photooxidation rate on the following parameters: (i) substrate concentration: (ii) catalyst amount: and (iii) pH was alos investigated. At the used experimental conditions the substrate photooxidation rate follows a pseudo-first order kinetics with respect to the substrate concentration. The presence of S{sub 2}O{sub 8}''2 enhances the reaction rate more that when H{sub 2}O{sub 2} was added. (Author) 20 refs.

  5. Synthesis and Characterization of Mn–C–Codoped TiO2 Nanoparticles and Photocatalytic Degradation of Methyl Orange Dye under Sunlight Irradiation

    Directory of Open Access Journals (Sweden)

    Wei Xin

    2012-01-01

    Full Text Available Novel visible-light-active Mn–C–TiO2 nanoparticles were synthesized by modified sol-gel method based on the self-assembly technique using polyoxyethylenes orbitan monooleate (Tween 80 as template and carbon precursor and manganese acetate as manganese precursor. The samples were characterized by XRD, FTIR, UV-vis diffuse reflectance, XPS, and laser particle size analysis. The XRD results showed that Mn–C–TiO2 sample exhibited anatase phase and no other crystal phase was identified. High specific surface area, small crystallite size, and small particle size distribution could be obtained by manganese and carbon codoped and Mn–C–TiO2 exhibited greater red shift in absorption edge of samples in visible region than that of C–TiO2 and pure TiO2. The photocatalytic activity of synthesized catalyst was evaluated by photocatalytic oxidation of methyl orange (MO solution under the sunlight irradiation. The results showed that Mn–C–TiO2 nanoparticles have higher activity than other samples under sunlight, which could be attributed to the high specific surface area, smaller particle size, and lower band gap energy.

  6. One step synthesis and characterization of copper doped sulfated titania and its enhanced photocatalytic activity in visible light by degradation of methyl orange

    Institute of Scientific and Technical Information of China (English)

    Radha Devi Chekuri; Siva Rao Tirukkovalluri

    2016-01-01

    This paper reports on the synthesis of copper doped sulfated titania nano-crystalline powders with varying (2.0%–10.0%, by mass) by single step sol gel method. The synthesized photo catalyst has been characterized by employing various techniques like X-ray Diffraction (XRD), Ultraviolet–Visible Diffuse Reflection Spectroscopy (UV–Vis DRS), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM), Energy Dispersive Spectrometry (EDS), Fourier Transform Infrared Spectroscopic Studies (FT-IR), and Transmission Electron Microscopy (TEM). From the XRD and TEM results, al the samples were reported in anatase phase with reduction in particle size in the range of 7 to 12 nm. SEM indicated the change in morphology of the particles. The presence of copper in titania lattice was evidenced by XPS. From UV–Vis DRS and FT-IR studies indicated that prominent absorption shift is observed towards visible region (red shift), the entry of Cu2+into TiO2 lattice as a substitution-al dopant and SO42− ions were covalently bonded with Ti4+ on the surface of the copper doped titania respectively. The photocatalytic activity studies were investigated by considering methyl orange (MO) as dye pol utant in the presence of the visible light. The effect of various parameters like effect of dosage of the catalyst, dopant concentration, pH of the solution, and concentration of the dye was studied in detail.

  7. Visible light-degradation of azo dye methyl orange using TiO2/β-FeOOH as a heterogeneous photo-Fenton-like catalyst.

    Science.gov (United States)

    Xu, Zhihui; Zhang, Ming; Wu, Jingyu; Liang, Jianru; Zhou, Lixiang; L, Bo

    2013-01-01

    In this study, a novel TiO2/β-FeOOH composite photocatalyst was synthesized by a hydrothermal method. X-ray diffraction, Fourier transform infrared spectrum, UV-vis diffuse reflectance spectra and scanning electron microscopy (SEM) were used to characterize the composite photocatalyst. The photocatalytic activity of the prepared composite photocatalyst was evaluated in a heterogeneous photo-Fenton-like process using methyl orange (MO) as target pollutant. The TiO2/β-FeOOH composites exhibited higher photocatalytic activity than pure β-FeOOH and TiO2 under visible-light irradiation. The enhanced photocatalytic activity can be ascribed to the formation of TiO2/β-FeOOH heterostructure, which plays an important role in expanding the photoactivity to the visible light region and in effectively prolonging the lifetime of photoinduced electrons and holes. Further investigation revealed that the 25TiO2/β-FeOOH composite synthesized with the TiO2/Fe(3+) in a mole ratio of 25:75 showed the highest catalytic activity.

  8. Photocatalytic degradation of methyl orange by CeO2 and Fe-doped CeO2 films under visible light irradiation.

    Science.gov (United States)

    Channei, D; Inceesungvorn, B; Wetchakun, N; Ukritnukun, S; Nattestad, A; Chen, J; Phanichphant, S

    2014-08-29

    Undoped CeO2 and 0.50-5.00 mol% Fe-doped CeO2 nanoparticles were prepared by a homogeneous precipitation combined with homogeneous/impreganation method, and applied as photocatalyst films prepared by a doctor blade technique. The superior photocatalytic performances of the Fe-doped CeO2 films, compared with undoped CeO2 films, was ascribed mainly to a decrease in band gap energy and an increase in specific surface area of the material. The presence of Fe(3+) as found from XPS analysis, may act as electron acceptor and/or hole donor, facilitating longer lived charge carrier separation in Fe-doped CeO2 films as confirmed by photoluminescence spectroscopy. The 1.50 mol% Fe-doped CeO2 film was found to be the optimal iron doping concentration for MO degradation in this study.

  9. Bi(1-x)Ni(x)VO(4-y) Solid Solution with a High Visible-Light Photocatalytic Activity for Degradation Methyl Orange.

    Science.gov (United States)

    Wang Jing; Wei, Yuelin; Huang, Yunfang; Wu, Jihuai; Dong, Qiang; Yin, Shu; Sato, Tsugio

    2015-09-01

    Particulate solid solutions Bi(1-x)Ni(x)VO(4-y) were synthesized by solid-state reaction at high temperature. The samples were characterized by X-ray Diffraction (XRD), Field-Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive Spectrometer (EDS), Brunauer-Emmett-Teller (BET) surface area and Ultraviolet-Visible spectroscopy (UV-Vis). The photocatalytic activity of BiVO4 for photocatalytic degradation of organic contaminants ability in visible light region could be improved by doping of Ni(2+). The high visible light photocatalytic activity of Bi(1-x)Ni(x)VO(4-y) solid solution might be due to the generation of a new band gap and expanding the range of visible light response. It was suggested that the Ni(2+) doping was beneficial to effective charge separation of Bi(1-x)Ni(x)VO(4-y) solid solution, thus improved the photocatalytic activity.

  10. CuO薄膜与过氧化氢协同光催化降解甲基橙%Cooperative Photocatalytic Degradation of Methyl Orange by H2O2 and CuO Thin Film

    Institute of Scientific and Technical Information of China (English)

    徐玲; 刘昌龄; 徐海燕; 吴世彪; 王峰; 李春艳

    2012-01-01

    In this study, we prepared CuO thin film from Cu(NO3)2 . 3H2O, ammonium hydroxide and NaOH by using chemical bath deposition (CBD) method. Structural characterization of the film has been made before and after photocatalytic reaction using XRD and SEM. CuO thin film was then applied to Methyl Orange solution containing H2O2. The reaction solution was collected for visible spectrophotome-try after certain periods of radiation under different light sources. Our experiments demonstrate that, opti-mal Methyl Orange degradation rate can be achieved with CuO film at surface area of 12. 50cm2, 40. OmL 3.0% H2O2 and pH=7 for the reaction system, under UV light. Under optimal conditions, 100. 0% deg-radation rate can be obtained in 10 min, whereas in 40 min in the absence of H2O2, indicating a cooperative effect on photocatalytic degradation of methyl orange by H2O2 and CuO thin film.%本文以Cu(NO3)2·3H2O为铜源,浓氨水为络合剂和NaOH调节溶液的pH,采用化学浴法(CBD)制备了CuO薄膜。通过X-射线衍射(XRD)和扫描电子显微镜(SEM)对其光催化前后的结构和形貌进行了表征。将CuO薄膜放在含有H2O2的甲基橙溶液中,经不同光源照射一定时间后,取其溶液进行可见分光光度分析来研究CuO薄膜的光催化性能。试验结果表明:紫外灯光源下,当催化剂CuO薄膜的表面积为12.50cm2、3.0%H2O2用量为40.0ml、pH=7时,降解甲基橙溶液的效果较好,光照10min后降解率就达到100.0%;不加H2O2时,需光照40min降解率才能达到100.0%,说明H2O2对CuO膜光催化降解甲基橙起到协同促进作用。

  11. Experimental Study of Degradation of Methyl Blue by Metal -ion-catalyzed Ozonation%金属离子催化臭氧降解甲基蓝染料的试验研究

    Institute of Scientific and Technical Information of China (English)

    程谣; 赵冬梅; 饶力; 郝小龙

    2013-01-01

      以甲基蓝为目标污染物,在常规臭氧氧化体系中引入了废水中常见的金属离子,如 Fe2+、Cu2+、Mn2+,形成均相臭氧催化体系进行试验,结果表明:能提高臭氧的氧化降解效率。在初始甲基蓝浓度为40 mg/L ,pH值为4~6的条件下,Fe2+、Mn2+和Cu2+3种离子的最佳投加量分别为0.1 mg/L、0.5 mg/L和1.0 mg/L ,3种离子的催化能力顺序为Fe2+≈ Mn2+﹥Cu2+。%  Taking methyl blue as model compounds ,this article introduces the common metal ions ,such as Fe 2+ 、Cu 2+ 、Mn 2+ ,into conventional ozone oxidation system to form homogeneous ozone catalytic system , and it can improve the efficiency of ozone degradation efficiency .When the initial concentration of methyl blue is 40 mg/L and pH value is in the range of 4~6 ,the optimal dosages of Fe 2+ ,Mn 2+ and Cu 2+ are respectively 0 .1mg/L ,0 .5 mg/L , 1 .0 mg/L ,and the order of catalytic abilities of three metal ions is Fe 2+ ≈Mn 2+﹥Cu 2+ .

  12. Synthesis and characterization of C-doped TiO2 thin films for visible-light-induced photocatalytic degradation of methyl orange

    Science.gov (United States)

    Hassan, Mohamed Elfatih; Cong, Longchao; Liu, Guanglong; Zhu, Duanwei; Cai, Jianbo

    2014-03-01

    C-TiO2 thin films were synthesized by a modified sol-gel route based on the self-assembly technique exploiting Tween80 (T80) as a pore directing agent and carbon source. The effect of calcination time on the photocatalytic activity of C-doped TiO2 catalyst was studied. The samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transforms infrared (FTIR), UV-vis diffuse reflectance spectroscopy, and photoluminescence spectra (PL). The XRD results showed that C-TiO2 sample calcined at 400 °C for various times exhibited anatase phase and no other crystal phase was identified. C-TiO2 exhibited a shift in an absorption edge of samples in the visible region than that of conventional or reference TiO2. The XPS results showed an existence of C in the TiO2 catalysts and C might be existed as Csbnd Osbnd Ti group. Moreover, the C-TiO2 thin film calcined at 400 °C for 30 min showed the lowest PL intensity due to a decrease in the recombination rate of photogenerated electrons and holes under UV light irradiation. Also the photocatalytic activity of synthesized catalyst was evaluated by decomposition of methyl orange (MO) under visible light irradiation. The results showed that the optimum preparations of C-TiO2 thin films were found to be under calcination temperature of 400, calcination time of 30 min, and with preparation 9 layers film.

  13. Optimization of protoplast fusion conditions of bacteria able to de-grade bensulfuron-methyl and butachlor%苄嘧磺隆和丁草胺降解菌原生质体融合条件优化

    Institute of Scientific and Technical Information of China (English)

    李春艳; 吴志洋; 冯丽萍; 熊明华; 成小松

    2014-01-01

    In this study, functional fusants with dual functions to simultaneously degrade bensulfuron-methyl and butachlor were constructed through protoplast fusion of Rhodococcus sp. BX2 and Acinetobacter sp.LYC-1. The protoplast fusion condition was optimized and finally the fusion frequency reached to 2.67 × 10-7 under the following condition:40%of PEG4000, 10 min, 35℃, 500μL of freshly-prepared calcium phosphate, pH 7.5. The fusant F1 was obtained with the use of penicillin G and fosfomycin as selection markers and determined to be able to pass more than eight generations stablely on the plates containing bensulfuron-methyl and butachlor. The fusant F1 had respective high degradation rate of 65.35%BSM and 62.41%butachlor in mineral medium supplemented by BSM 100 mg·L-1 and butachlor 100 mg·L-1.%研究以苄嘧磺隆降解菌Rhodococcus sp. BX2与丁草胺降解菌Acinetobacter sp. LYC-1为亲本,优化用于构建可同时降解苄嘧磺隆与丁草胺的融合子的原生质体融合条件。通过单因素试验和正交试验,确定原生质体融合的最佳条件:PEG400040%、35℃、10 min,500μL新生磷酸钙溶液,pH 7.5,此条件下融合频率达到2.67×10-7。以青霉素和磷霉素作为筛选的遗传标记,最终获得在含有上述两种除草剂的无机盐培养基中可稳定继代培养8代以上的融合子F1。该融合子在含有100 mg·mL-1苄嘧磺隆和100 mg·mL-1丁草胺的无机盐培养基中,F1的降解率分别为65.35%和62.41%。

  14. Analysis on the Influencing Factors of Photocatalytic Degradation of Methyl Orange by SnO2/Sodium Titanate Nanotubes%SnO2/钛酸钠纳米管降解甲基橙的影响因素分析

    Institute of Scientific and Technical Information of China (English)

    张红美; 孔德国; 杨瑛; 罗华平

    2013-01-01

    Methyl orange was photocatalytically degradated using SnO2/sodium titanate nanotubes.The effects of initial concentration of methyl orange,pH,light source,catalyst loading,cycle number and illuminative time on the degradation rate were studied.The results indicated that when the dosage of catalyst was 0.03 g in 50 mL of the 5 mg/L methyl orange with pH 5.15,the degradation rate of methyl orange reached 96.4% after UV radiation for 80 minutes.%以SnO2/钛酸钠纳米管为催化剂对甲基橙进行光催化降解,研究甲基橙浓度、溶液pH、光源、催化剂用量、循环次数及光照时间对降解率的影响.结果表明,在甲基橙浓度为5 mg/L、pH 5.15、溶液体积为50 mL时投加0.03 g的催化剂,紫外光照射80 min后,甲基橙的降解率达到96.4%.

  15. Synthesis and characterization of C-doped TiO{sub 2} thin films for visible-light-induced photocatalytic degradation of methyl orange

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, Mohamed Elfatih; Cong, Longchao; Liu, Guanglong, E-mail: liugl@mail.hzau.edu.cn; Zhu, Duanwei; Cai, Jianbo

    2014-03-01

    Graphical abstract: - Highlights: • C-TiO{sub 2} thin films were successfully synthesized by modified sol–gel method based on the self-assembly technique. • Tween 80, one kind of hydrocarbon surfactants, was used as template and carbon precursor. • A thorough material characterization was performed to determine the effect of calcination time on the structural and optical properties of the synthesized catalyst films. - Abstract: C-TiO{sub 2} thin films were synthesized by a modified sol–gel route based on the self-assembly technique exploiting Tween80 (T80) as a pore directing agent and carbon source. The effect of calcination time on the photocatalytic activity of C-doped TiO{sub 2} catalyst was studied. The samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transforms infrared (FTIR), UV–vis diffuse reflectance spectroscopy, and photoluminescence spectra (PL). The XRD results showed that C-TiO{sub 2} sample calcined at 400 °C for various times exhibited anatase phase and no other crystal phase was identified. C-TiO{sub 2} exhibited a shift in an absorption edge of samples in the visible region than that of conventional or reference TiO{sub 2}. The XPS results showed an existence of C in the TiO{sub 2} catalysts and C might be existed as C-O-Ti group. Moreover, the C-TiO{sub 2} thin film calcined at 400 °C for 30 min showed the lowest PL intensity due to a decrease in the recombination rate of photogenerated electrons and holes under UV light irradiation. Also the photocatalytic activity of synthesized catalyst was evaluated by decomposition of methyl orange (MO) under visible light irradiation. The results showed that the optimum preparations of C-TiO{sub 2} thin films were found to be under calcination temperature of 400, calcination time of 30 min, and with preparation 9 layers film.

  16. 纳米零价锌降解甲基橙效率探讨%Discussion on efficiency of methyl orange degradation by nanoscale zero-valent zinc particles

    Institute of Scientific and Technical Information of China (English)

    夏立珍; 王树林; 邱迎新; 赵立峰

    2014-01-01

    The ordinary zinc powder was milled for 1 3 h with roller vibration milling and produced irregular sheet nanoscale zero-valent zinc particles(NZVZ).The particle size was between 20 and 30 nm.This paper here was focused on the degradation of water soluble methyl orange(MO)by NZVZ,and rotation speed of magnetic stirrer,NZVZ dosage,initial MO concentration and NaCl dosage were studied systematically.It was found that the degradation of MO with 2 g/L of NZVZ was 98.5% in 60 min,which was 60.3% higher than that of using 4 g/L of ordinary zinc powder,the sulfanilic acid and 1 ,4-benzenediamine,N,N-dimethyl-as degradation pro-gress products were identified.Degradation was enhanced with increase of rotation speed and NZVZ dosage, while decreased with increase of initial MO concentration.Moreover,the existence of NaCl can promote the re-action procress and degradation increased with increase of NaCl dosage.Kinetic analyses based on the experi-mental data elucidated that the degradation process followed the pseudo first-order kinetic equation.%将普通零价锌在滚压振动磨中研磨13 h后,制备出不规则片状、粒径为20~30 nm的纳米零价锌(NZVZ)。采用所制备的 NZVZ 降解甲基橙,系统研究了搅拌速度、NZVZ 投入量、甲基橙初始浓度和NaCl的加入对甲基橙降解效率的影响。结果表明, NZVZ表面反应活性增高,反应60 min 时,2 g/L 的NZVZ对甲基橙降解率为98.5%,比4 g/L 的普通零价锌高60.3%,其中间降解产物有对氨基苯磺酸和对氨基二甲基苯胺。降解率随转速、NZVZ 投入量的增加而升高,随 MO 初始浓度的增加而降低;加入 NaCl能促进反应进行,且随着投入量增加降解率增加。通过对实验数据的分析,验证 NZVZ降解 MO 过程符合伪一级动力学方程式。

  17. Fabrication of highly active Melem/Zn{sub 0.25}Cd{sub 0.75}S composites for the degradation of bisphenol A and methyl orange under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiaodong [School of Civil Engineering and Architecture, University of Jinan, Jinan 250022 (China); Yan, Tao, E-mail: yantujn@163.com [School of Resources and Environment, University of Jinan, Jinan 250022 (China); Liu, Xiaohuan; Ji, Pengge [School of Civil Engineering and Architecture, University of Jinan, Jinan 250022 (China); Sun, Meng; Wei, Dong; Yan, Liangguo; Du, Bin [School of Resources and Environment, University of Jinan, Jinan 250022 (China)

    2016-11-30

    Highlights: • Novel Melem/Zn{sub 0.25}Cd{sub 0.75}S composite showed enhanced activity in MO degradation. • The composites with melem content of 30 wt.% exhibited the best activity. • The heterojunction was in situ fabricated between melem and Zn{sub 0.25}Cd{sub 0.75}S. • The Melem/Zn{sub 0.25}Cd{sub 0.75}S heterojunction facilitated the separation of electron-hole pairs. - Abstract: Metal-free polymeric catalyst hold great promise owing to their abundant sources, low-cost fabrication and easy processibility. Melem, an important intermediate during condensation of melamine rings to graphitic carbon nitride (g-C{sub 3}N{sub 4}), was synthesized by simple solid phase polymerization process. A novel Melem/Zn{sub 0.25}Cd{sub 0.75}S composite was fabricated through a facile one-step hydrothermal method. The as-products were characterized by X-ray diffraction (XRD), UV–vis DRS spectroscopy, fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM). The TEM and HRTEM results reveal that Zn{sub 0.25}Cd{sub 0.75}S nanoparticles and Melem closely contact with each other to form an intimate interface. The as-prepared composites exhibit significantly enhanced visible light photocatalytic performance for the degradation of Methyl orange (MO) and Bisphenol A (BPA), which could be attributed to the effective photo-induced charges transfer and separation in Melem/Zn{sub 0.25}Cd{sub 0.75}S composites. On the basis of radical scavenger experiments, superoxide radicals and holes are suggested to play a critical role in MO degradation over Melem/Zn{sub 0.25}Cd{sub 0.75}S heterojunctions. A possible mechanism for charge separation and transfer in the Melem/Zn{sub 0.25}Cd{sub 0.75}S composites was proposed to explain the enhanced photocatalytic performance.

  18. 三维电极反应器对甲基叔丁基醚降解性能的试验研究%Experiment on degradation of methyl tert-butylether by using 3D electrode reactor

    Institute of Scientific and Technical Information of China (English)

    徐苏云; 何传秋; 罗丽雯; 董亚楠; 王水寒

    2014-01-01

    Methyl tert-butyl ether ( MTBE) is a potential carcinogen pollutant.This article investigated the electrochemical degradation of MTBE in wastewater by using a novel three-dimensional electrode re-actor with granular activated carbon as particle electrode.The effects of electrolyte, voltage intensity and pH level on the degradation of MTBE were tested.Experiment results show that under the conditions of 25℃, electrolyte (Na2SO4) concentration of 0.2 mol, potential=10 V and pH=7.0, total organic car-bon ( TOC) of MTBE solution with initial concentration of 50 mmol is removed by 78% after 150 min. Compared to activated carbon adsorption and bipolar electrolysis, the three-dimensional electrode reac-tor can greatly improve the efficiency of MTBE degradation and carbonization.Therefor, the three-di-mensional electrode reactor is an effective technology to remove MTBE contamination in wastewater and has better application prospect.%甲基叔丁基醚( MTBE)是一种潜在的致癌污染物质,本文考察了以活性炭为粒子电极的三维电极反应器对水体中MTBE的降解性能。实验分别研究了电解质、电压强度和pH值对MTBE降解效果的影响。结果表明:当温度为25℃、电解质Na2 SO4浓度为0.2 mol、电压为10V、pH为7.0的条件下,初始浓度为50 mmol的MTBE溶液,在反应进行150 min后其总有机碳的去除率可达78%。与单纯活性炭吸附、两极电解对比,三维电极能大幅度提高MTBE的降解和碳化效率。因此三维电极反应器是一种能够有效去除废水中MTBE污染的技术方法,具备较好的应用前景。

  19. DNA Methylation

    OpenAIRE

    Alokail, Majed S.; Alenad, Amal M.

    2015-01-01

    The DNA of E. coli contains 19,120 6-methyladenines and 12,045 5-methylcytosines in addition to the four regular bases and these are formed by the postreplicative action of three DNA methyltransferases. The majority of the methylated bases are formed by the Dam and Dcm methyltransferases encoded by the dam (DNA adenine methyltransferase) and dcm (DNA cytosine methyltransferase) genes. Although not essential, Dam methylation is important for strand discrimination during repair of replication e...

  20. Application of response surface methodology for degradation of methyl orange with TiO{sub 2} sol-gel sulphated Ti; Aplicacion de metodologia de superficie de respuesta para la degradacion de naranja de metilo con TiO{sub 2} sol-gel sulfatado

    Energy Technology Data Exchange (ETDEWEB)

    Del Angel S, M. T.; Garcia A, R. [Instituto Tecnologico de Ciudad Madero, Av. 1o. de Mayo y Sor Juana I. de la Cruz, Col. Los Mangos, 89440 Ciudad Madero, Tamaulipas (Mexico); Garcia A, P.; Lagunes G, L. M. [Universidad Juarez Autonoma de Tabasco, Division Academica de Ciencias Agropecuarias, Av. Universidad s/n, Zona de la Cultura, Col. Magisterial, 86040 Villahermosa, Tabasco (Mexico); Cabrera C, E. G., E-mail: shish_kko@yahoo.com.mx [Instituto Tecnologico de Villahermosa, Carretera Villahermosa-Frontera Km. 3.5, Cd. Industrial, 86010 Villahermosa, Tabasco (Mexico)

    2015-06-01

    In this work we report the implementation of the response surface methodology for the optimization of photo catalytic degradation of methyl orange dye (MO) using as photo catalyst sulphated TiO{sub 2} prepared by sol-gel method. The variables studied were ph of the solution (3-11), catalyst concentration (0.1-1 g/L), and MO concentration (10-30 ppm). The effects of these parameters over the degradation of MO were evaluated according to a Box-Behnken design. The only crystal structure identified by X-ray diffraction was anatase phase. The optimum conditions for the photo catalytic degradation of MO according to the methodology applied were ph 6.0, 17.78 ppm MO concentration at each concentration level of the catalyst. (Author)

  1. Kinetics of the methylation of a platinum(II) diimine dithiolate complex

    Energy Technology Data Exchange (ETDEWEB)

    Stace, Justin J.; Ball, P. J.; Shingade, Vikas; Chatterjee, Sayandev; Shiveley, Amber; Fleeman, Wendi L.; Staniszewski, Aaron J.; Krause, Jeanette A.; Connick, William B.

    2016-06-01

    Pt(dbbpy)(bdt) and Pt(tmphen)(bdt) (dbbpy = 4,4'-di-t-butyl-2,2'-bipyridine; tmphen = 3,4,7,8-tetramethyl-1,10-phenanthroline; bdt2- = 1,2-benzenedithiolate) are reported. Pt(dbbpy)(bdt) reacts with one equivalent of methyl iodide to give the S-methylated product, [Pt(dbbpy)(CH3bdt)]I. The reaction follows second order kinetics with a rate constant of 1.3×10 2 M-1s-1 at 311 K. The accumulated data are consistent with direct nucleophilic attack by the coordinated bdt2- ligand sulfur atom on the carbon atom of the methyl iodide. Variable-temperature experiments yield an Arrhenius activation energy of 51 ± 3 kJ/mol. Activated complex reaction theory yields an enthalpy and entropy of activation of 48 ± 2 kJ/mol and 125 ± 7 J/(mol K), respectively, consistent with an SN2 reaction mechanism. The structure of the monosulfinate adduct, Pt(dbbpy)(bdtO2), also is reported. The fluid-solution luminescence of Pt(tmphen)(bdt) is concentration dependent and characterized by a 1591 ± 41 ns lifetime and 2.6 ± 0.2% quantum yield at infinite dilution.

  2. DNA methylation

    DEFF Research Database (Denmark)

    Williams, Kristine; Christensen, Jesper; Helin, Kristian

    2012-01-01

    DNA methylation is involved in key cellular processes, including X-chromosome inactivation, imprinting and transcriptional silencing of specific genes and repetitive elements. DNA methylation patterns are frequently perturbed in human diseases such as imprinting disorders and cancer. The recent...... discovery that the three members of the TET protein family can convert 5-methylcytosine (5mC) into 5-hydroxymethylcytosine (5hmC) has provided a potential mechanism leading to DNA demethylation. Moreover, the demonstration that TET2 is frequently mutated in haematopoietic tumours suggests that the TET...... proteins are important regulators of cellular identity. Here, we review the current knowledge regarding the function of the TET proteins, and discuss various mechanisms by which they contribute to transcriptional control. We propose that the TET proteins have an important role in regulating DNA methylation...

  3. TiO2/ACF的Sol-Gel法制备及其对甲基橙的去除历程%A new method of preparing TiO2/ACF via solgel and its degradation mechanism for methyl orange

    Institute of Scientific and Technical Information of China (English)

    孙剑; 刘守新

    2011-01-01

    采用溶胶-凝胶法制备了TiO2/ACF复合材料.采用SEM、低温液氮吸附对TiO2/ACF复合材料的结构进行表征.以甲基橙为模型物考察TiO2/ACF对液相有机污染物的去除性能.通过液相色谱-质谱联用技术(HPLC-MS)检测紫外光照射下TiO2/ACF和TiO2去除甲基橙过程中中间产物的种类与分布.结果表明:随着涂覆次数增加,复合材料比表面积下降,TiO2涂层变厚、开裂,部分TiO2脱落;煅烧温度决定TiO2晶型结构和晶粒尺寸.涂覆2次、煅烧温度450 ℃所得TiO2/ACF具有最高催化活性,100 min内对甲基橙的去除率高达100%,且循环使用5次后对甲基橙的去除率仍可达83.4%.ACF的负载减少了甲基橙去除过程中中间产物的种类和含量.在以TiO2为光催化剂时检测到3种中间产物,甲基橙主要经过中间产物的路径被降解;而在TiO2/ACF上以直接光催化降解为主,中间产物种类、数量均低于TiO2.%The present paper is to introduce a via sol-gel method of preparing TiO2/ACF composite and the degradation mechanism for methyl orange. In order to develop the method of preparing the composite, we adopted the scanning electronic microscopy (SEM), N2 (77 K) adsorption and X-ray diffraction to identify the characteristics of the composites and Methyl orange(MO) in addition to developing the compound model for testing the organic removal activity and HPLC-MS used for intermediate detection. The results of our study show that the calcination temperature and dip-coating times are the two principal influential factors on the activities of TiO2/ACF. With the increase of the dip-coating time length and the decrease of the surface area of TiO2/ACF as the TiO2 film turned to be thicker, then got split and eventually fell off. It was found that the complete anatase was formed into the sample calcinated at the temperature of 450 ℃ and the anatase phase transformation to rutile at 750 ℃. The crystal size of TiO2 was found to decrease

  4. Catalytic degradation of methyl orange using Fenton-like mesoporous Fe-MCM-41%类Fenton试剂MCM-41负载Fe催化降解甲基橙的研究

    Institute of Scientific and Technical Information of China (English)

    田志茗; 袁昊; 杜玺

    2015-01-01

    通过浸渍法制备了MCM-41负载铁催化剂Fe-MCM-41,采用XRD、UV-vis光谱、N2吸附-脱附分析和SEM等对Fe-MCM-41进行表征,结果表明,Fe-MCM-41具有载体MCM-41的介孔结构,孔道分布均匀,平均孔径1.88 nm.研究了以Fe-MCM-41为催化剂的类Fenton体系对甲基橙染料快速降解的方法,考察了分子筛中Fe含量、H2O2及甲基橙初始浓度、溶液pH和催化剂用量等条件对染料降解率的影响.当pH=3、H2O2及甲基橙初始浓度分别为30 mmol/L和20 mmol/L、催化剂用量为2 g/L、反应60 min时,甲基橙的降解率可达96.82%.动力学研究表明,采用Fe-MCM-41催化降解甲基橙遵循一级反应动力学模型(R=0.992),对应的速率常数为8.51×10-2 min-1.%Loaded catalyst of Fe- MCM- 41 was prepared by impregnation method and characterized by means of XRD, UV- vis, N2 adsorption- desorption and SEM. The results indicated that Fe- MCM- 41 had typi⁃cal mesoporous structure features with uniform pore size distribution. The average pore diameter was 1.88 nm. Rapid decolorization of methyl orange by Fenton- like mesoporous Fe- MCM- 41 as catalyst was investi⁃gated. The effects of various parameters such as initial pH, initial H2O2 concentration, dosage of catalyst and initial dye concentration on decolorization rate were studied. The optimum reaction conditions were initial pH=3, the initial concentration of H2O2 30 mmol/L, the initial concentration of methylene blue 20 mmol/L, the dos⁃age of catalyst 2 g/L. The removal rate of methyl orange was 96.82% under the optimum conditions after 60 min of degradation time. The kinetic models indicated that the first order kinetics fit wel with the data (R=0.992) and the corresponding rate constant was 8.51×10- 2 min- 1.

  5. Study on preparation of solid superacid SO2-4/Fe2O3 and photocatalytic degradation of methyl orange%SO2-4/Fe2O3固体超强酸的制备及光催化降解甲基橙的研究

    Institute of Scientific and Technical Information of China (English)

    王占领

    2011-01-01

    The SO 4 /Fe2O3 solid superacid catalyst was prepared by chemical precipitating and soaking method, and the effect of photocatalytic degradation to methyl orange was studied with the single-factor experiment method. The results showed that when the catalyst quantity is 2g·L-1, Ph value is 6, the first concentration of methyl orange is 10mg·L-1 and reactive time is 90min, the degradation ratio of methyl orange is over 90%.%采用沉淀-浸渍法制备SO2-4/Fe2O3固体超强酸催化剂.通过单因素实验考察了SO2-4/Fe2O3光降解甲基橙的效果.结果表明,固体超强酸SO2-4/Fe2O3光催化降解甲基橙的最优反应条件是:溶液pH值为6,催化用量2g·L-1,甲基橙溶液初始浓度10mg·L-1,反应时间90min.在最优反应条件下,甲基橙的降解率可达90%以上.

  6. TiO2纳米管阵列薄膜光电催化降解甲基橙染料废水%Photoelectrocatalytic Degradation of Methyl Orange in Aqueous Solution over TiO2 Nanotubes Array

    Institute of Scientific and Technical Information of China (English)

    周凝; 薛建军; 王玲; 凌世盛; 蔡燕华; 钱佳燕; 黄明喜

    2011-01-01

    The photoelectrocatalytic degradation of a model textile dye, methyl orange (MO), using titanium dioxide(TiO2) nanotubes array mesh as photocatalyst was investigated TiO2 nanotubes array mesh was prepared by electrochemical anodization technique, and was characterized by X-ray diffraction and FE-SEM microscopy. The differences between the photoiysis and photocatalysis as well as photo-elect-catalysis, and the effects of pH, external bias were examined. The first-order kinetic model was applied to describe the photoelectrocatalytic (PEC) oxidation as well It was found that the optimum conditions were pH = 3, bias 1. 5V in the PEC system, the degration rate can reach 100% after 80min later, in this condition. This investigation showed that PEC oxidation was a convenient way to mineralise the organic matters with high effciency.%采用电化学阳极氧化法在纯钛表面制备出TiO2纳米管阵列,应用FE-SEM和XRD表征其形貌.以该纳米管陈列薄膜为光阳极,比较了光解、光催化和光电催化对甲基橙溶液降解效率的差异,研究了pH值和外加偏压对甲基橙降解效率的影响,并建立了光电催化氧化反应的一级动力学模型来描述产生这种效果的主要因素.结果表明,在光电催化氧化体系中,TiO2纳米管阵列薄膜对甲基橙具有显著的降解作用;溶液中的电解质、溶液的pH值和外加偏压是影响光电催化效果的关键因素;最佳的降解条件为电解质存在下、pH值为3、外加偏压为1.5V,在该条件下紫外灯照射80min后降解率可达100%.

  7. Tris(Cyclopentadienyl)Uranium-t-Butyl: Synthesis, reactions, and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Weydert, M.

    1993-04-01

    Compounds (RC{sub 5}H{sub 4}){sub 3}U(t-Bu) were prepared for R = H, Me, Et. Their decomposition products in aromatic solvents are consistent with a radical decomposition pathway induced by solvent-assisted U-C bond homolysis. NMR was used to study the reactions of (RC{sub 5}H{sub 4}){sub 3}UCl with t-BuLi (R = t-Bu, Me{sub 3}Si). Reactions of (MeC{sub 5}H{sub 4}){sub 3}U(t-Bu) with Lewis bases and fluorocarbons were studied. Analogous reaction chemistry between (RC{sub 5}H{sub 4}){sub 3}ThX systems and t-BuLi was also studied, and reactivity differences between U and Th are discussed. Synthesis of sterically crowded (RC{sub 5}H{sub 4}){sub 4}U compounds is next considered. Reaction of the trivalent (RC{sub 5}H{sub 4}){sub 3}U with (RC{sub 5}H{sub 4}){sub 2}Hg results in formation of (RC{sub 5}H{sub 4}){sub 4}U. Steric congestion, cyclopentadienyl ligand exchange, and electron transfer are discussed. (DLC)

  8. Tris(Cyclopentadienyl)Uranium-t-Butyl: Synthesis, reactions, and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Weydert, M.

    1993-04-01

    Compounds (RC[sub 5]H[sub 4])[sub 3]U(t-Bu) were prepared for R = H, Me, Et. Their decomposition products in aromatic solvents are consistent with a radical decomposition pathway induced by solvent-assisted U-C bond homolysis. NMR was used to study the reactions of (RC[sub 5]H[sub 4])[sub 3]UCl with t-BuLi (R = t-Bu, Me[sub 3]Si). Reactions of (MeC[sub 5]H[sub 4])[sub 3]U(t-Bu) with Lewis bases and fluorocarbons were studied. Analogous reaction chemistry between (RC[sub 5]H[sub 4])[sub 3]ThX systems and t-BuLi was also studied, and reactivity differences between U and Th are discussed. Synthesis of sterically crowded (RC[sub 5]H[sub 4])[sub 4]U compounds is next considered. Reaction of the trivalent (RC[sub 5]H[sub 4])[sub 3]U with (RC[sub 5]H[sub 4])[sub 2]Hg results in formation of (RC[sub 5]H[sub 4])[sub 4]U. Steric congestion, cyclopentadienyl ligand exchange, and electron transfer are discussed. (DLC)

  9. Catalytic Potential of Nano-Magnesium Oxide on Degradation of Humic Acids From Aquatic Solutions

    Directory of Open Access Journals (Sweden)

    Ghorban Asgari

    2014-12-01

    Full Text Available Catalytic ozonation is a new and promising process used to remove the contaminants from drinking water and wastewater. This study aimed to evaluate the catalytic potential of nano-magnesium oxide (nano-MgO for the removal of humic acids (HA from water. Mg (NO32 solution was used to prepare MgO powder by the calcination method. In a semi-batch reactor, the catalytic ozonation was carried out. The effects of the various operating parameters, including pH, reaction time, T-butyl alcohol (TBA and phosphate on HA degradation were evaluated. Experimental results indicated that degradation of HA was increased as the pH solution and reaction time were increased. Maximum HA degradation was obtained at pH = 10 and the reaction time of 10 minutes in the catalytic process. The calculated catalytic potential of nano-MgO on ozonation of HA was 60%. Moreover, catalytic ozonation process was not affected by TBA and the main reaction on HA degradation HA have effect take place on MgO surface. According to the results of this study, the developed MgO catalyst is the active and proficient catalyst in HA degradation using the catalytic ozonation process.

  10. Methyl gallate

    Directory of Open Access Journals (Sweden)

    Silvina Pagola

    2009-02-01

    Full Text Available The crystal structure of the title compound (systematic name: methyl 3,4,5-trihydroxybenzoate, C8H8O5, is composed of essentially planar molecules [maximum departures from the mean carbon and oxygen skeleton plane of 0.0348 (10 Å]. The H atoms of the three hydroxyl groups, which function as hydrogen-bond donors and acceptors simultaneously, are oriented in the same direction around the aromatic ring. In addition to two intramolecular hydrogen bonds, each molecule is hydrogen bonded to six others, creating a three-dimensional hydrogen-bonded network.

  11. EFECTO DE LA CONCENTRACIÓN DEL METIL PARATIÓN Y EL EXTRACTO DE LEVADURA COMO FACTORES DE SELECCIÓN DE MICROORGANISMOS DEGRADADORES DEL PESTICIDA A PARTIR DE SUELOS CONTAMINADOS Effect of Methyl Parathion Concentration and Yeast Extract as Factors for Selecting Pesticide Degrading Microorganisms from Polluted Soils

    Directory of Open Access Journals (Sweden)

    L. R. Botero

    2011-12-01

    Full Text Available El aislamiento y cultivo de microorganismos con capacidades para degradar los contaminantes ambientales es importante para implementar planes de biorremediación. En este estudio se evaluó el efecto del extracto de levadura tanto en la capacidad de asimilación microbiana del pesticida organofosforado metil paratión, como en los procesos de aislamiento de microorganismos útiles para de degradar este pesticida. Los microorganismos evaluados fueron obtenidos de suelo fresco fumigado históricamente con este pesticida. Los ensayos se efectuaron con medios sólidos definidos enriquecidos con metil paratión (0-60 mg L-1 y extracto de levadura (0-0.5 g L -1. Se encontró que los microorganismos fueron capaces de asimilar hasta 5 mg L -1 del metil paratión en ausencia de extracto de levadura sin evidenciar efectos tóxicos. La capacidad de asimilación aumentó a 10 mg L-1 en los cultivos enriquecidos con 0.5 g L-1 de extracto de levadura. El extracto de levadura en las dosis usadas no afectó el aislamiento de microorganismos. Sin embargo, el aislamiento por siembra directa en medios enriquecidos con metil paratión como única fuente de carbono se dificultó por el aporte de la materia orgánica del suelo que permitió el crecimiento de cepas tolerantes sin capacidad para degradar el pesticida.Isolation and culture of microorganisms with capacity to degrade environmental pollutants are important for implementing bioremediation plans. This study is an evaluation of the yeast extract effect on both the microbial capacity to assimilate the organo-phosphorous pesticide methyl parathion and the isolation processes of microorganisms useful for degrading this pesticide. Microorganisms evaluated were obtained from fresh soil historically fumigate with this pesticide. Trials were conducted with defined solid means enriched with methyl parathion (0-60 mg L-1 and yeast extract (0-0.5 g L-1. It was found that microorganisms were able to assimilate up to 5

  12. Degradation of carbofuran by ozonation.

    Science.gov (United States)

    Suneethi, S; Joseph, Kurian

    2009-04-01

    Degradation of commercial grade carbofuran (2, 3 dihydro-2, 2-dimethyl-7 benzo furanyl-N-methyl carbamate) in aqueous solution by ozone oxidation was investigated using bench scale experiments. The degradation rate was strongly influenced by the ozone dosage, pH, initial concentration of carbofuran and contact time of ozonation. Carbofuran solution of 200ppm concentration was degraded by 79% within 10 minutes consuming 87 mg of ozone at pH 4. The associated TOC reduction was observed to be 53%. Ammonium (20 mg/L) and nitrate (30 mg/L) ions were detected in the effluent as degradation products of ozonation. The results support the effectiveness of ozonation for degradation of organic pesticides such as carbofuran.

  13. 两株分解除草剂丁·苄的双效菌株筛选、鉴定及其降解特性研究%A Study on Screening, Identification and Degradation Characteristics of Two Strains with Double Effects on Butachlor and Bensulfuron Methyl

    Institute of Scientific and Technical Information of China (English)

    刘军; 霍光华

    2011-01-01

    为了获得能同时分解丁草胺和苄嘧磺隆的菌株,从连续施用丁·苄3年以上的水稻田土壤中分离筛选出15株能以丁草胺和苄嘧磺隆为唯一碳源的菌株,进一步复筛获得了两株菌Dx9、Dx12.通过ITS序列分析确定Dx9与青霉属的Penicillium expansum Y2-08( GU134896),Dx12与曲霉属的Aspergillus fumigatus( FM999061)均有99%同源性.在底物浓度为100 mg/L(20%丁·苄500 mg/L),pH 7.0,培养温度为35℃,摇床转速为180 r/min的条件下,接种1.0 mL( 107 cfu/mL)培养72 h,Dx9对丁草胺和苄嘧磺隆的降解率分别为87.3%和95.6%,Dx12对丁草胺和苄嘧磺隆的降解率分别为92.1%和88.5%.由此可见,该两菌株对除草剂丁·苄污染的土壤具有较好地生物修复作用.%Two strains of fungi D×9 and D×l2 capable of simultaneously degrading butachlor and bensulfu-ron methyl were obtained from primarily screened fifteen strains which only degradate butachlor or bensulfuron methyl from paddy field soil which was applied with butachlor and bensulfuron methyl for over three years. Based on the phylogenetic analysis of ITS sequence, the strains D×9 and D×l2 were identified as 99% homologous with Penicillium expansum Y2-08( GU134896) and Aspergillus Jumigatus ( FM999061) respectively. The degradation rates of strain D×9 on butachlor and bensulfuron methyl were 87. 3% and 95. 6% , while the rates of strain D×l2 were 92. 1% and 88. 5% at the concentration of 100 mg/L(20% butachlor and bensulfuron methyl 500 mg/L) and under the condition of 30 ℃ , pH 7.0, 180 r/min, inoculation 1 x 107 cfu/mL and incubation 72 h. Judging from this, the strains D×9 and D×l2 are of good bioremediation function for soil polluted by herbicides of butachlor and bensulfuron methyl.

  14. Study on the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chloro-phenoxyacetic sodium (MCPA sodium) in natural agriculture-soils of Fuzhou, China using capillary electrophoresis.

    Science.gov (United States)

    Fu, Fengfu; Xiao, Linxia; Wang, Wei; Xu, Xueqin; Xu, Liangjun; Qi, Guomin; Chen, Guonan

    2009-03-01

    A new method of analyzing trace 2,4-Dichlorophenoxyacetic acid (2,4-D) and 2-methy-4-chloro-lphenoxyacetic sodium (MCPA sodium) in soils by capillary electrophoresis (CE) has been developed in this study. The optimum analytical conditions including chemical component and concentration of buffer solution, pH, separation voltage and sample injection time were studied in detail. Under the optimum conditions, 2,4-D and MCPA sodium in soils can be speedy separated and determined within 20 min with detection limits of 0.15 microg/g (2,4-D) and 0.25 microg/g (MCPA sodium) , a RSD (n=6)89%. With the help of analytical method developed in this study, the degradations of 2,4-D and MCPA sodium in natural agriculture-soils of Fuzhou were studied. The experimental results indicated that the degradations of 2,4-D and MCPA sodium follow first-order kinetics with degradation constants of 0.1509 day(-1) (2,4-D) and 0.2722 day(-1) (MCPA sodium) respectively. The degradation half-life were calculated to be 4.6 days (2,4-D) and 2.6 days (MCPA sodium) at 27 degrees C, implied that 2,4-D and MCPA sodium can be speedy degraded in natural agriculture-soils of Fuzhou, China.

  15. TiO2-SBA-15负载镧催化剂的制备、表征及光催化降解甲基橙%Preparation,Characterization and Photocatalytic Degradation Methylic Orange of TiO2-SBA-15 with Lanthanum Loading Catalyst

    Institute of Scientific and Technical Information of China (English)

    徐玲; 姜宇; 赵婷婷; 高晓杰; 任睿

    2016-01-01

    Using SBA-15 as carrier and tetrabutyl titanate as titanium source,the SBA-15 molecular sieve loaded with TiO 2 was prepared by sol-gel method. The different mass concentrations of lanthanum nitrate were loaded onto TiO 2-SBA-15 by impregnation method, and TiO 2-SDA-15 catalysts with different lanthanum loading were prepared by high temperature calcination method. The series of catalysts were characterized by X-ray diffraction (XRD),infrared spectrum (FT-IR), inductively coupled plasma (ICP)emission spectrum,transmission electron microscopy (TEM)and N2 adsorption-desorption isotherm.The TiO 2-SBA-15 catalysts with different La mass contents were used as photo-catalysts to degrade the solution of methyl orange.We investigated the effect of La loading mass content on the degradation rate of methyl orange.The experimental results show that the degradation rate of methyl orange is 100% when La loading mass content is 0.14% and UV lamp irradiation for 140 min.%以 SBA-15为载体,钛酸四丁酯为钛源,采用溶胶-凝胶法制备负载 TiO 2的 SBA-15分子筛,先通过浸渍法将不同质量浓度的硝酸镧负载到 TiO 2-SBA-15上,再用高温焙烧法制备不同镧负载量的 TiO 2-SBA-15催化剂.采用 X 射线衍射(XRD)、红外光谱(FT-IR)、电感耦合等离子体(ICP)发射光谱、透射电镜(TEM)及 N2吸附-脱附等温线对系列催化剂进行表征.用负载镧的 TiO 2-SBA-15催化剂对甲基橙溶液进行光降解,考察镧的负载量对甲基橙降解率的影响.实验结果表明:当镧的负载量为0.14%,紫外灯照射140 min 时,甲基橙的降解率为100%.

  16. A convenient method to generate methylated and un-methylated control DNA in methylation studies

    Directory of Open Access Journals (Sweden)

    Mehdi Manoochehri

    2013-09-01

    Full Text Available Methylated and un-methylated control DNA is an important part of DNA methylation studies. Although human and mouse DNA methylation control sets are commercially available, in case of methylation studies on other species such as animals, plants, and bacteria, control sets need to be prepared. In this paper a simple method of generating methylated and un-methylated control DNA is described. Whole genome amplification and enzymatic methylation were performed to generate un-methylated and methylated DNA. The generated DNA were confirmed using methylation sensitive/dependant enzymes, and methylation specific PCR. Control reaction assays confirmed the generated methylated and un-methylated DNA.

  17. LIQUID CULTURE FOR ISOLATING MICROORGANISMS WITH POTENTIAL TO DEGRADE METHYL PARATHION FROM AGRICULTURAL SOILS AND ORGANIC WASTE CULTIVO LÍQUIDO PARA AISLAR MICROORGANISMOS CON POTENCIAL PARA DEGRADAR METIL PARATIÓN A PARTIR DE SUELOS AGRÍCOLAS Y RESIDUOS ORGÁNICOS

    Directory of Open Access Journals (Sweden)

    L. R. Botero

    2012-12-01

    Full Text Available The search for microorganisms with high capacity for pesticide degradation is a very interesting attempt to approach bioremediation strategies in order to prevent contamination. This study evaluates the potential of agricultural soils and solid organic waste cultures microbial isolation as a strategy for screening microorganisms with potential for Methyl parathion (MP degradation. For the study, microbial consortia were recovered from the liquid fraction of suspension cultures of agricultural soils and solid organic waste. Then, the MP degradation ability and its toxic effect on microbial activity were determined during microbial incubations under laboratory controlled conditions. The results showed that it is not possible to recover the active microorganisms that have potential to degrade the MP from the agricultural soils. However, an active consortium that would degrade both MP and its degradation products was isolated from the organic solid waste.La búsqueda de microorganismos con alta capacidad de degradación de los plaguicidas es un intento muy interesante de acercarse a las estrategias de biorremediación con el fin de evitar la contaminación. Este estudio evalúa el potencial del cultivo de microorganismos de suelos agrícolas y de residuos sólidos orgánicos como una estrategia para la detección de microorganismos con potencial para el metil paratión (MP la degradación. Para el estudio, consorcios microbianos fueron recuperados de la fracción líquida de los cultivos en suspensión de los suelos agrícolas y los residuos sólidos orgánicos. La capacidad de degradación de la MP y su efecto tóxico sobre la actividad microbiana se determinó durante las incubaciones de los microorganismos en condiciones controladas de laboratorio. Los resultados mostraron que no es posible recuperar los microorganismos activos que tienen potencial para degradar el MP de los suelos agrícolas. Sin embargo, un consorcio activo que degradar

  18. The effect of natural iron oxide and oxalic acid on the photocatalytic degradation of isoproturon: a kinetics and analytical study.

    Science.gov (United States)

    Boucheloukh, H; Remache, W; Parrino, F; Sehili, T; Mechakra, H

    2017-03-27

    The photocatalytic degradation of isoproturon, a persistent toxic herbicide, was investigated in the presence of natural iron oxide and oxalic acid and under UV irradiation. The influence of the relevant parameters such as the pH and the iron oxide and oxalic acid concentrations has been studied. The presence of natural iron oxide and oxalic acid in the system effectively allow the degradation of isoproturon, whereas the presence of t-butyl alcohol adversely affects the phototransformation of the target pollutant, thus indicating that an OH radical initiated the degradation mechanism. The degradation mechanism of isoproturon was investigated by means of GC-MS analysis. Oxidation of both the terminal N-(CH3)2 and isopropyl groups is the initial process leading to N-monodemethylated (NHCH3), N-formyl (N(CH3)CHO), and CHCH3OH as the main intermediates. The substitution of the isopropyl group by an OH group is also observed as a side process.

  19. Dissociation dynamics of methylal

    Energy Technology Data Exchange (ETDEWEB)

    Beaud, P.; Frey, H.-M.; Gerber, T.; Mischler, B.; Radi, P.P.; Tzannis, A.-P. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    The dissociation of methylal is investigated using mass spectrometry, combined with a pyrolytic radical source and femtosecond pump probe experiments. Based on preliminary results two reaction paths of methylal dissociation are proposed and discussed. (author) 4 fig., 3 refs.

  20. Mutation of glutamic acid 103 of toluene o-xylene monooxygenase as a means to control the catabolic efficiency of a recombinant upper pathway for degradation of methylated aromatic compounds.

    Science.gov (United States)

    Cafaro, Valeria; Notomista, Eugenio; Capasso, Paola; Di Donato, Alberto

    2005-08-01

    Toluene o-xylene monooxygenase (ToMO) and phenol hydroxylase (PH) of Pseudomonas stutzeri OX1 act sequentially in a recombinant upper pathway for the degradation of aromatic hydrocarbons. The catalytic efficiency and regioselectivity of these enzymes optimize the degradation of growth substrates like toluene and o-xylene. For example, the sequential monooxygenation of o-xylene by ToMO and PH leads to almost exclusive production of 3,4-dimethylcatechol (3,4-DMC), the only isomer that can be further metabolized by the P. stutzeri meta pathway. We investigated the possibility of producing ToMO mutants with modified regioselectivity compared with the regioselectivity of the wild-type protein in order to alter the ability of the recombinant upper pathway to produce methylcatechol isomers from toluene and to produce 3,4-DMC from o-xylene. The combination of mutant (E103G)-ToMO and PH increased the production of 4-methylcatechol from toluene and increased the formation of 3,4-DMC from o-xylene. These data strongly support the idea that the products and efficiency of the metabolic pathway can be controlled not only through mutations that increase the catalytic efficiency of the enzymes involved but also through tuning the substrate specificity and regioselectivity of the enzymes. These findings are crucial for the development of future metabolic engineering strategies.

  1. 基于构建微生物传感器的甲基对硫磷降解菌的分离鉴定及其降解特性研究%Isolation and Characterization of Methyl Parathion-degrading Bacteria Based on Microbial Sensor Construction

    Institute of Scientific and Technical Information of China (English)

    耿芳芳; 王慧; 秦伟; 丁保君

    2014-01-01

    have been widely used for environmental analysis. In this paper, four novel bacterial strains capable of utilizing methyl parathion as the sole carbon source were isolated from pesticide contaminated soils. These four isolates were identified based on morphological characteristics and 16S rRNA gene sequences analysis, and their capability of degrading methyl parathion were investigated by high performance liquid chromatography. The highest degrading efficiency strain was selected for further study of degrading mechanism. The results indicated that degradation rate of these four strains were all over 78%after incubation at 30 ℃, pH 7.0 for 7 d with the original concentration of methyl parathion 50 mg·L-1. The highest degradation rate was up to 100%. 16S rRNA gene sequences indicated that strain MP-6 was affiliated into the genus klebsiella. The LC-MS results indicated that methyl parathion was hydrolyzed to dimethyl thiophosphoric acid and p-nitrophenol by MP-6. A little of p-nitrophenol molecules could be further metabolized to 4-nitrocatechol and 1, 2, 4-benzenetrio. The results indicated that based on detecting the potential signal of intermediate product p-nitrophenol, the strain MP-6 could be used to construct microbial sen-sors for determination of organophosphorus pesticides in environment.

  2. Electrolytic treatment of methyl orange in aqueous solution using three-dimensional electrode reactor coupling ultrasonics.

    Science.gov (United States)

    He, Pingting; Wang, Ling; Xue, Jianjun; Cao, Zhibin

    2010-04-01

    The treatment of wastewater containing methyl orange was investigated experimentally using a three-dimensional electrode reactor coupling ultrasonics and the effect of ultrasonics on the degradation was studied. The effects of cell voltage, original concentration of methyl orange, pH value and the concentration of electrolyte on the removal efficiency were considered. The experimental results indicated that the removal rate of methyl orange exceeded 99% and the removal of chemical oxygen demand (COD(Cr)) approached 84% under the optimum conditions. Using ultraviolet-visible spectrum analysis, a general degradation pathway for methyl orange was proposed based on the analysis of intermediate compounds. According to the ultraviolet-visible spectral changes during degradation of methyl orange, it can be presumed that the removal of COD(Cr) lags behind the removal of methyl orange because the structure of the benzene ring was more difficult to destroy compared with the azo double bonds.

  3. Enrichment of methylated DNA by methyl-CpG immunoprecipitation.

    Science.gov (United States)

    Sonnet, Miriam; Baer, Constance; Rehli, Michael; Weichenhan, Dieter; Plass, Christoph

    2013-01-01

    Normal DNA methylation is an epigenetic modification required for proper development. Aberrant DNA methylation, in contrast, is frequently observed in many different malignancies including leukemias and lymphomas. Global DNA methylation profiling addresses the methylated sequences (methylome) of patient genomes to identify disease-specific methylation patterns. Workload in methylome analyses can be considerably reduced by methylome enrichment using proteins or antibodies with high affinity to methylated DNA. Methyl-CpG Immunoprecipitation (MCIp) employs an immobilized recombinant human methyl-CpG binding domain protein 2, MBD2, which binds methylated CpGs in double-stranded DNA. Elution with increasing salt concentrations allows the fractionated enrichment of different degrees of methylation.

  4. Degradation and induction specificity in actinomycetes that degrade p-nitrophenol.

    OpenAIRE

    1993-01-01

    We have isolated two soil bacteria (identified as Arthrobacter aurescens TW17 and Nocardia sp. strain TW2) capable of degrading p-nitrophenol (PNP) and numerous other phenolic compounds. A. aurescens TW17 contains a large plasmid which correlated with the PNP degradation phenotype. Degradation of PNP by A. aurescens TW17 was induced by preexposure to PNP, 4-nitrocatechol, 3-methyl-4-nitrophenol, or m-nitrophenol, whereas PNP degradation by Nocardia sp. strain TW2 was induced by PNP, 4-nitroca...

  5. N、Zn共掺杂纳米TiO2光催化剂的制备及其光催化降解甲基橙应用研究%Preparation of N/Zn Co-doped Nano TiO2 and Its Application in Photocatalytic Degradation of Methyl Orange

    Institute of Scientific and Technical Information of China (English)

    陆茜

    2012-01-01

    N.Zn co-doped TiO2 nanometer photo-catalysts(NZT), which have photo-catalysis in invisible spectral rang, were prepared with TiOSO4 and ZnSO4·7H2O as raw materials, NH3·H2O as precipitant by co-precipitation method. It was characterized by XRD and UV-VIS. Photo-catalytic activities of N、Zn co-doped TiO2 catalysts under visible light irradiation by photo-degradation of methyl orange. Verification experiment in the optimum conditions showed that the degradation ratio of methyl reached 98.2%, under sunshine for 6h, with ultrasound dispersing and whipping, and it's still 74.2% four times reused.%以TiOSO4和ZnSO4·7H2O为原料,NH3·H2O为沉淀剂,采用超声波-微波化学共沉淀法制备具有可见光催化活性的N、Zn共掺杂纳米TiO2纳米粉体,并用XRD、UV-VIS对其进行了表征.在可见光下,考察了N、Zn共掺杂纳米TiO2光催化降解甲基橙的光催化性能.通过正交试验得出降解甲基橙的最佳工艺条件,并在最佳条件下做验证实验得出在太阳光下照射6h,光催化剂重复使用4次后降解率仍可到达74.2%,有超声分散、搅拌的条件下降解甲基橙降解率达到98.2%.

  6. ANTI-BIOFOULING BY DEGRADATION OF POLYMERS

    Institute of Scientific and Technical Information of China (English)

    Chun-feng Ma; Hong-jun Yang; Guang-zhao Zhang

    2012-01-01

    Copolymers of methyl methacrylate (MMA) and acrylate terminated poly(ethylene oxide-co-ethylene carbonate)(PEOC) macromonomer (PEOCA) were synthesized,and the degradation of the polymers was investigated by use of quartz crystal microbalance with dissipation (QCM-D).It is shown that the polymeric surface exhibits degradation in seawater depending on the content of the side chains.Field tests in seawater show that the surface constructed by the copolymer can effectively inhibit marine biofouling because it can be self-renewed due to degradation of the copolymer.

  7. Experimental and theoretical studies on stability of new stabilizers for N-methyl-P-nitroaniline derivative in CMDB propellants.

    Science.gov (United States)

    Tang, Qiufan; Fan, Xuezhong; Li, Jizhen; Bi, Fuqiang; Fu, Xiaolong; Zhai, Lianjie

    2017-04-05

    Although N-methyl-P-nitroaniline (MNA) was a quite effective stabilizer in composite modified double base (CMDB) propellants, it undergoes crystallization easily from nitroglycerin (NG) during storage. In order to improve its solubility in nitroglycerin (NG) and the stability in propellants, several new stabilizers including N-ethyl-p-nitroaniline (ENA), N-n-propyl-p-nitroaniline (n-PNA), N-i-propyl-p-nitroaniline (i-PNA), N-n-butyl-p-nitroaniline (n-BNA) and N-t-butyl-p-nitroaniline (t-BNA) were designed and synthesized to replace MNA by increasing the carbon chain length. The interaction between NG and different stabilizers was simulation by Materials Studio 5.5 and the stability and the high temperature stability performance of those new stabilizers in propellants were calculated by Gaussian 09. It was found that both the solubility of new stabilizers in NG and the stability and the high temperature stability performance of those in propellants were improved when the carbon chain length of substitution groups on nitrogen atom was increased. Thus, the n-BNA was a most potential stabilizer. Then all properties of the stabilizers were studied experimentally, which was agreement well with the theoretical analysis.

  8. [DNA methylation and epigenetics].

    Science.gov (United States)

    Vaniushin, B F

    2006-09-01

    In eukaryotic cells, nuclear DNA is subject to enzymatic methylation with the formation of 5-methylcytosine residues, mostly within the CG and CNG sequences. In plants and animals this DNA methylation is species-, tissue-, and organelle-specific. It changes (decreases) with age and is regulated by hormones. On the other hand, genome methylation can control hormonal signal. Replicative and post-replicative DNA methylation types are distinguished. They are mediated by multiple DNA methyltransferases with different site-specificity. Replication is accompanied by the appearance of hemimethylated DNA sites. Pronounced asymmetry of the DNA strand methylation disappears to the end of the cell cycle. A model of methylation-regulated DNA replication is proposed. DNA methylation controls all genetic processes in the cell (replication, transcription, DNA repair, recombination, and gene transposition). It is the mechanism of cell differentiation, gene discrimination and silencing. In animals, suppression of DNA methylation stops development (embryogenesis), switches on apoptosis, and is usually lethal. Disruption of DNA methylation pattern results in the malignant cell transformation and serves as one of the early diagnostic features of carcinogenesis. In malignant cell the pattern of DNA methylation, as well as the set of DNA methyltransferase activities, differs from that in normal cell. In plants inhibition of DNA methylation is accompanied by the induction of seed storage and florescence genes. In eukaryotes one and the same gene can be simultaneously methylated both at cytosine and adenine residues. It can be thus suggested, that the plant cell contains at least two different, and probably, interdependent systems of DNA methylation. The first eukaryotic adenine DNA methyltransferase was isolated from plants. This enzyme methylates DNA with the formation of N6-methyladenine residues in the sequence TGATCA (TGATCA-->TGm6ATCA). Plants possess AdoMet-dependent endonucleases

  9. Methyl vinyl glycolate as a diverse platform molecule

    DEFF Research Database (Denmark)

    Sølvhøj, Amanda Birgitte; Taarning, Esben; Madsen, Robert

    2016-01-01

    Methyl vinyl glycolate (methyl 2-hydroxybut-3-enoate, MVG) is available by zeolite catalyzed degradation of mono- and disaccharides and has the potential to become a renewable platform molecule for commercially relevant catalytic transformations. This is further illustrated here by the development...... and various long-chain terminal olefins give unsaturated α-hydroxy fatty acid methyl esters in good yields. [3,3]-Sigmatropic rearrangements of MVG also proceed in good yields to give unsaturated adipic acid derivatives. Finally, rearrangement of the allylic acetate of MVG proceeds in acceptable yield...

  10. Comparative analysis of rubber seed methyl ester with other methyl ...

    African Journals Online (AJOL)

    Comparative analysis of rubber seed methyl ester with other methyl esters. ... In order to achieve a two-step transesterification process was developed to convert rubber seed oil to its methyl esters. The first step, acid catalyzed ... Article Metrics.

  11. Polysaccharide Degradation

    Science.gov (United States)

    Stone, Bruce A.; Svensson, Birte; Collins, Michelle E.; Rastall, Robert A.

    An overview of current and potential enzymes used to degrade polysaccharides is presented. Such depolymerases are comprised of glycoside hydrolases, glycosyl transferases, phosphorylases and lyases, and their classification, active sites and action patterns are discussed. Additionally, the mechanisms that these enzymes use to cleave glycosidic linkages is reviewed as are inhibitors of depolymerase activity; reagents which react with amino acid residues, glycoside derivatives, transition state inhibitors and proteinaceous inhibitors. The characterization of various enzymes of microbial, animal or plant origin has led to their widespread use in the production of important oligosaccharides which can be incorporated into food stuffs. Sources of polysaccharides of particular interest in this chapter are those from plants and include inulin, dextran, xylan and pectin, as their hydrolysis products are purported to be functional foods in the context of gastrointestinal health. An alternative use of degraded polysaccharides is in the treatment of disease. The possibility exists to treat bacterial exopolysaccharide with lyases from bacteriophage to produce oligosaccharides exhibiting bioactive sequences. Although this area is currently in its infancy the knowledge is available to investigate further.

  12. 纳米复合材料ZnO/TiO_2-ZrO_2的制备及其微波辅助光催化降解甲基橙%Preparation of ZnO/TiO_2-ZrO_2 Nano-composites and the Activity of Microwave-assisted Photocatalytic Degradation of Methyl Orange

    Institute of Scientific and Technical Information of China (English)

    李莉; 陆丹; 赵月红; 李恩帅; 禚娜

    2011-01-01

    The three-component nano-composite ZnO/TiO2-ZrO2 was prepared by doping ZnO into binary-system TiO2-ZrO2 through calcined at 450℃ with a sol-gel-temperature solvothermal process in the presence of surfactant EO20PO70EO20(P123).The phase composition,structures and morphologies of as-prepared nanocomposites were characterized by XRD,transmission TEM,N2 adsorption-desorption tests and SEM assisted X-ray energy dispersive spectroscopy.The results showed that the material prepared possesses mesoporous structure,well distribution,regular morphologies,and existing titanium-zirconium oxide,and rough surface with some surface defects.Its behavior of microwave assisted photocatalytic degradation of methyl orange in aqueous solution was investigated.The results indicated that the methyl orange was degraded by 92.2% within 90 min,which means its photocatalytic activity is better than that of P25 and TiO2-ZrO2.%采用EO20PO70EO20(P123)作为模板剂,通过溶胶-凝胶-程序升温溶剂热一步法将金属氧化物ZnO掺杂到TiO2-ZrO2二元体系中,经过450℃煅烧,制备了三元纳米半导体复合材料ZnO/TiO2-ZrO2。通过X-射线衍射、氮气吸附-脱附测定、透射电子显微镜以及扫描电镜配合X-射线能量色散谱仪等测试手段对合成材料的组成、结构及形貌进行了表征。结果表明,该复合材料中存在钛锆氧化物,具有介孔结构。复合材料颗粒分布较均匀,结构较规整,表面具有一定的缺陷。以甲基橙为模型分子,探讨了所合成的复合材料的微波辅助光催化降解能力,发现其的光催化活性高于TiO2-ZrO2和市售P25,90 min内微波辅助光催化降解率可达92.2%。

  13. Citric Acid-Assisted Hydrothermal Synthesis of Bi2WO6 Nanosheets for Highly Efficient Degradation of Methyl Orange under Visible Light Irradiation%柠檬酸辅助水热法制备可见光高效去除甲基橙的Bi2WO6纳米片

    Institute of Scientific and Technical Information of China (English)

    陈渊; 刘国聪; 李志友; 黄苏萍; 周科朝

    2011-01-01

    Bi2WO6 nanosheets with highly efficient photocatalytic activity under visible light irradiation were prepared by a hydrothermal method using Bi(NO3)3·5H2O and Na2WO3·2H2O as starting materials and citric acid as the chelating agent. The properties of the as-prepared samples were investigated by X-ray diffraction, field emission high resolution transmission electron microscopy, Raman spec-troscopy, and UV-Vis diffusion reflectance spectroscopy. The photocatalytic properties of the Bi2WO6 catalyst were also investigated. The results show that Bi2WO6 nanosheets with orthorhombic structure can be obtained by adjusting the pH value of the reaction system. Compared with the Bi2WO6 catalyst prepared without citric acid, the Raman bands of the nanosheets assisted with citric acid present blue shift and show a significant red shift in the absorption band and its band gap was narrowed to 2.55 eV. The pH value of the reaction system is the main factor affecting the visible light-driven photocatalytic activity. The Bi2WO6 sample prepared at pH = 7.0 shows a higher photocatalytic activity. Over this catalyst, the 100% degradation of methyl orange solution (10 mg/L) is obtained after visible light irradiation for 15 min. In addition, after 5 recycles, there is no significant decrease in its photocatalytic activity, indicating that Bi2WO6 is a stable photocatalyst for degradation of methyl orange under visible light irradiation.%以Bi(NO3)3·5H2O和Na2WO3 ·2H2O为原料,以柠檬酸为络合剂,采用辅助水热法制备了Bi2WO6纳米片,运用X射线衍射、扫描电镜、场发射高分辨透射电镜、拉曼光谱、红外光谱和紫外-可见漫反射光谱等手段对样品进行了表征,并考察了该催化剂光催化去除甲基橙反应性能.结果表明,通过调节体系的pH值可制得结晶度良好的正交晶系钨铋矿型结构的Bi2WO6纳米片状晶体.柠檬酸的添加使得制备的Bi2WO6颗粒的拉曼光谱特征峰发生蓝移,紫外-可见

  14. Anaerobic Mercury Methylation and Demethylation by Geobacter bemidjiensis Bem.

    Science.gov (United States)

    Lu, Xia; Liu, Yurong; Johs, Alexander; Zhao, Linduo; Wang, Tieshan; Yang, Ziming; Lin, Hui; Elias, Dwayne A; Pierce, Eric M; Liang, Liyuan; Barkay, Tamar; Gu, Baohua

    2016-04-19

    Microbial methylation and demethylation are two competing processes controlling the net production and bioaccumulation of neurotoxic methylmercury (MeHg) in natural ecosystems. Although mercury (Hg) methylation by anaerobic microorganisms and demethylation by aerobic Hg-resistant bacteria have both been extensively studied, little attention has been given to MeHg degradation by anaerobic bacteria, particularly the iron-reducing bacterium Geobacter bemidjiensis Bem. Here we report, for the first time, that the strain G. bemidjiensis Bem can mediate a suite of Hg transformations, including Hg(II) reduction, Hg(0) oxidation, MeHg production and degradation under anoxic conditions. Results suggest that G. bemidjiensis utilizes a reductive demethylation pathway to degrade MeHg, with elemental Hg(0) as the major reaction product, possibly due to the presence of genes encoding homologues of an organomercurial lyase (MerB) and a mercuric reductase (MerA). In addition, the cells can strongly sorb Hg(II) and MeHg, reduce or oxidize Hg, resulting in both time and concentration-dependent Hg species transformations. Moderate concentrations (10-500 μM) of Hg-binding ligands such as cysteine enhance Hg(II) methylation but inhibit MeHg degradation. These findings indicate a cycle of Hg methylation and demethylation among anaerobic bacteria, thereby influencing net MeHg production in anoxic water and sediments.

  15. ENZYMOLOGY OF ARSENIC METHYLATION

    Science.gov (United States)

    Enzymology of Arsenic MethylationDavid J. Thomas, Pharmacokinetics Branch, Experimental Toxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park...

  16. Lysine methylation: beyond histones

    Institute of Scientific and Technical Information of China (English)

    Xi Zhang; Hong Wen; Xiaobing Shi

    2012-01-01

    Posttranslational modifications (PTMs) of histone proteins,such as acetylation,methylation,phosphorylation,and ubiquitylation,play essential roles in regulating chromatin dynamics.Combinations of different modifications on the histone proteins,termed 'histone code' in many cases,extend the information potential of the genetic code by regulating DNA at the epigenetic level.Many PTMs occur on non-histone proteins as well as histones,regulating protein-protein interactions,stability,localization,and/or enzymatic activities of proteins involved in diverse cellular processes.Although protein phosphorylation,ubiquitylation,and acetylation have been extensively studied,only a few proteins other than histones have been reported that can be modified by lysine methylation.This review summarizes the current progress on lysine methylation of nonhistone proteins,and we propose that lysine methylation,like phosphorylation and acetylation,is a common PTM that regulates proteins in diverse cellular processes.

  17. Degradation and induction specificity in actinomycetes that degrade p-nitrophenol

    Energy Technology Data Exchange (ETDEWEB)

    Hanne, L.F.; Kirk, L.L.; Appel, S.M.; Narayan, A.D.; Bains, K.K. (California State Univ., Chico, CA (United States))

    1993-10-01

    We have isolated two soil bacteria (identified as Arthrobacter aurescens TW17 and Nocardia sp. strain TW2) capable of degrading p-nitrophenol (PNP) and numerous other phenolic compounds. A. aurescens TW17 contains a large plasmid which correlated with the PNP degradation phenotype. Degradation of PNP by A. aurescens TW 17 was induced by preexposure to PNP, 4-nitrocatechol, 3-methyl-4-nitrophenol, or m-nitrophenol, whereas PNP degradation by Nocardia sp. strain TW2 was induced by PNP, 4-nitrocatechol, phenol, p-cresol, or m-nitrophenol. A. aurescens TW17 initially degraded PNP to hydroquinone and nitrite. Nocardia sp. strain TW2 initially converted PNP to hydroquinone or 4-nitrocatechol, depending upon the inducing compound.

  18. Characterization of Ni and B Doped Nanosized TiO2 supported on haydite and Its Appfication in Degradation of Methyl Orange%Ni、B共掺杂TiO2-陶粒表征及降解甲基橙研究

    Institute of Scientific and Technical Information of China (English)

    王德英; 相龙玲

    2011-01-01

    Ni2O3 and B doped nanosized TiO2 supported on haydite were prepared by sol-sel method and studied by X-ray diffraction spectrum(XRD) and FT-IR Spectrometer. The results shoved that B into the TiO2 lattice combined with. Ti ion and replaced the O ion position, Ni with a molecule Nigh floated free outside a metallic crystal lattice. Dopants of Ni and B made TiO2 in the Bx-TiO2-yNi2O3-haydite catalyst partible size smaller and specific surface larger, effectively prevented electron-hole pairs recombined and helped to separate charges in order to improve photocatalytic activity of the catalyst. Methyl orange was used as the target pollutant and discussed the rule that composite photocatalyst degraded COD. The photocatalysis capability of the catalysts and influencing factors of photocatalysis degradation were studied, such as the catalyst calcination temperature, dosage of Ni and B, dosage of catalyst, the initial pH value. The results indicated that when the catalyst was sintered at 600℃, it had the best property of photocatalysis;The best doping dosage of B and Ni was 3. 0%.Asdosage of catalyst and the initial pH value decreased, the degradation rate of COD increased.%陶粒负载Ni2O3和B元素共掺杂纳米TiO2可见光催化剂采用溶胶-凝胶法制备.经XRD和FT—IR表征分析。可得B离子的掺杂是以取代晶格中的O离子的形式存在,Ni是以Ni2O3形式游离于TiO2表面存在。通过实验分析可知:B、Ni的掺杂使Bx-TiO2-,Ni2O3/陶粒催化剂中TiO2粒径减小、比表面积增大,同时抑制电子与空穴对的复合。有利于电荷分离.从而使催化剂光催化活性提高.以甲基橙为目标污染物,探讨了复合光催化剂光催他氧化降解COD的规律,同时考察了催化剂的焙烧温度、Ni元素和B元素掺杂量、催化剂投加量、初始pH值等因素对甲基橙COD去除效果的影响。结果表明:在600℃温度下焙烧的催化剂具有最佳光催化活

  19. Treatment of methyl orange dye wastewater by cooperative electrochemical oxidation in anodic-cathodic compartment.

    Science.gov (United States)

    Pang, L; Wang, H; Bian, Z Y

    2013-01-01

    Electrochemical oxidation of methyl orange wastewater was studied using Ti/IrO(2)/RuO(2) anode and a self-made Pd/C O(2)-fed cathode in the divided cell with a terylene diaphragm. The result indicated that the appropriate rate of feeding air improved the methyl orange removal efficiency. The discoloration efficiency of methyl orange in the divided cell increased with increasing current density. The initial pH value had some effect on the discoloration of methyl orange, which became not obvious when the pH ranged from 2 to 10. However, the average removal efficiency of methyl orange wastewater in terms of total organic carbon (TOC) can reach 89.3%. The methyl orange structure had changed in the electrolytic process, and the characteristic absorption peak of methyl orange was about 470 nm. With the extension of electrolysis time, the concentration of methyl orange gradually reduced; wastewater discoloration rate increased gradually. The degradation of methyl orange was assumed to be cooperative oxidation by direct or indirect electrochemical oxidation at the anode and H(2)O(2), ·OH, O(2)(-)· produced by oxygen reduction at the cathode in the divided cell. Therefore, the cooperative electrochemical oxidation of methyl orange wastewater in the anodic-cathodic compartment had better degradation effects.

  20. The interaction of radiation-generated radicals with myoglobin in aqueous solution—V. The indirect action of 2-methyl-2-hydroxypropyl radicals on oxymyoglobin

    Science.gov (United States)

    Whitburn, Kevin D.; Hoffman, Morton Z.

    The interaction of radiation-generated 2-methyl-2-hydroxypropyl radicals (derived from t-butyl alcohol) with oxymyoglobin has been examined at pH 7.3. In N 2O-saturated solutions, oxymyoglobin is converted to the ferri and ferryl derivatives of myoglobin; the production of ferrylmyoglobin is essentially eliminated when catalase is present in solution during irradiation. In deaerated solutions containing catalase, oxymyoglobin is converted to both ferro- and ferrimyoglobin during irradiation. When added O 2 is initially present, all compositional changes occur after irradiation; the presence of catalase diminishes, but does not eliminate, the extent of these postirradiation conversions of oxymyoglobin to the ferri and ferryl derivatives. These observations are interpreted in terms of the scavenging of the 2-methyl-2-hydroxypropyl radicals by O 2 to generate their peroxy analogs, which causes a displacement of the equilibrium between oxy- and ferromyoglobin. The peroxy radicals decay to produce H 2O 2, an organic peroxide, and other products. These peroxides subsequently react with ferromyoglobin to produce the ferryl form; the rate of the reaction increases with decreasing [O 2] as [ferromyoglobin] increases. This reaction is sufficiently fast in deaerated solution that substantial conversion of ferromyoglobin to ferrylmyoglobin occurs during the time of irradiation. The formation of the ferryl derivative in the presence of unconverted ferromyoglobin drives a concurrent synproportion reaction which produces ferrimyoglobin. Overall, no direct interaction of 2-methyl-2-hydroxypropyl radicals, nor their peroxy analogs, with myoglobin is indicated; all reactivity is accountable by the peroxide products of these radicals.

  1. Rheological behavior, chemical and physical characterization of soybean and cottonseed methyl esters submitted to thermal oxidation process

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Adriano Sant' ana; Silva, Flavio Luiz Honorato da; Lima, Ezenildo Emanuel de; Carvalho, Maria Wilma N.C. [Universidade Federal de Campina Grande (CCT/UFCG), PB (Brazil). Centro de Ciencia e Tecnologia; Dantas, Hemeval Jales; Farias, Paulo de Almeida [Universidade Federal de Campina Grande (CTRN/UFCG), PB (Brazil). Centro de Tecnologia e Recursos Naturais

    2008-07-01

    In this study the effect of antioxidant terc-butylhydroxyanisol (BHA) on the oxidative stability of soybean and cottonseed methyl esters subjected to thermal degradation at 100 deg C was studied. Soybean and cottonseed methyl esters specific mass, dynamic viscosity and rheological behavior were evaluated. According to results, antioxidant degraded samples specific mass and dynamic viscosity did not showed alterations, remaining statistically equal. Soybean and cottonseed methyl esters showed a Newtonian rheological behavior and degraded samples without adding BHA showed rheological behavior alterations. (author)

  2. Rheological behavior, chemical and physical characterization of soybean and cottonseed methyl esters submitted to thermal oxidation process

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Adriano Sant' ana; Silva, Flavio Luiz Honorato da; Lima, Ezenildo Emanuel de; Carvalho, Maria Wilma N.C. [Universidade Federal de Campina Grande (CCT/UFCG), PB (Brazil). Centro de Ciencia e Tecnologia; Dantas, Hemeval Jales; Farias, Paulo de Almeida [Universidade Federal de Campina Grande (CTRN/UFCG), PB (Brazil). Centro de Tecnologia e Recursos Naturais

    2008-07-01

    In this study the effect of antioxidant terc-butylhydroxyanisol (BHA) on the oxidative stability of soybean and cottonseed methyl esters subjected to thermal degradation at 100 deg C was studied. Soybean and cottonseed methyl esters specific mass, dynamic viscosity and rheological behavior were evaluated. According to results, antioxidant degraded samples specific mass and dynamic viscosity did not showed alterations, remaining statistically equal. Soybean and cottonseed methyl esters showed a Newtonian rheological behavior and degraded samples without adding BHA showed rheological behavior alterations. (author)

  3. Engineering of bacterial methyl ketone synthesis for biofuels.

    Science.gov (United States)

    Goh, Ee-Been; Baidoo, Edward E K; Keasling, Jay D; Beller, Harry R

    2012-01-01

    We have engineered Escherichia coli to overproduce saturated and monounsaturated aliphatic methyl ketones in the C₁₁ to C₁₅ (diesel) range; this group of methyl ketones includes 2-undecanone and 2-tridecanone, which are of importance to the flavor and fragrance industry and also have favorable cetane numbers (as we report here). We describe specific improvements that resulted in a 700-fold enhancement in methyl ketone titer relative to that of a fatty acid-overproducing E. coli strain, including the following: (i) overproduction of β-ketoacyl coenzyme A (CoA) thioesters achieved by modification of the β-oxidation pathway (specifically, overexpression of a heterologous acyl-CoA oxidase and native FadB and chromosomal deletion of fadA) and (ii) overexpression of a native thioesterase (FadM). FadM was previously associated with oleic acid degradation, not methyl ketone synthesis, but outperformed a recently identified methyl ketone synthase (Solanum habrochaites MKS2 [ShMKS2], a thioesterase from wild tomato) in β-ketoacyl-CoA-overproducing strains tested. Whole-genome transcriptional (microarray) studies led to the discovery that FadM is a valuable catalyst for enhancing methyl ketone production. The use of a two-phase system with decane enhanced methyl ketone production by 4- to 7-fold in addition to increases from genetic modifications.

  4. DNA methylation in obesity

    Directory of Open Access Journals (Sweden)

    Małgorzata Pokrywka

    2014-11-01

    Full Text Available The number of overweight and obese people is increasing at an alarming rate, especially in the developed and developing countries. Obesity is a major risk factor for diabetes, cardiovascular disease, and cancer, and in consequence for premature death. The development of obesity results from the interplay of both genetic and environmental factors, which include sedentary life style and abnormal eating habits. In the past few years a number of events accompanying obesity, affecting expression of genes which are not directly connected with the DNA base sequence (e.g. epigenetic changes, have been described. Epigenetic processes include DNA methylation, histone modifications such as acetylation, methylation, phosphorylation, ubiquitination, and sumoylation, as well as non-coding micro-RNA (miRNA synthesis. In this review, the known changes in the profile of DNA methylation as a factor affecting obesity and its complications are described.

  5. Apoptosis and DNA Methylation

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Huan X.; Hackett, James A. [MRC Human Genetics Unit, IGMM, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Nestor, Colm [MRC Human Genetics Unit, IGMM, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Breakthrough Research Unit, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Dunican, Donncha S.; Madej, Monika; Reddington, James P. [MRC Human Genetics Unit, IGMM, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Pennings, Sari [Queen' s Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ (United Kingdom); Harrison, David J. [Breakthrough Research Unit, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Meehan, Richard R., E-mail: Richard.Meehan@hgu.mrc.ac.uk [MRC Human Genetics Unit, IGMM, Western General Hospital, Edinburgh EH4 2XU (United Kingdom); Breakthrough Research Unit, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU (United Kingdom)

    2011-04-01

    Epigenetic mechanisms assist in maintaining gene expression patterns and cellular properties in developing and adult tissues. The molecular pathology of disease states frequently includes perturbation of DNA and histone methylation patterns, which can activate apoptotic pathways associated with maintenance of genome integrity. This perspective focuses on the pathways linking DNA methyltransferases and methyl-CpG binding proteins to apoptosis, and includes new bioinformatic analyses to characterize the evolutionary origin of two G/T mismatch-specific thymine DNA glycosylases, MBD4 and TDG.

  6. Apoptosis and DNA Methylation

    Directory of Open Access Journals (Sweden)

    Richard R. Meehan

    2011-04-01

    Full Text Available Epigenetic mechanisms assist in maintaining gene expression patterns and cellular properties in developing and adult tissues. The molecular pathology of disease states frequently includes perturbation of DNA and histone methylation patterns, which can activate apoptotic pathways associated with maintenance of genome integrity. This perspective focuses on the pathways linking DNA methyltransferases and methyl-CpG binding proteins to apoptosis, and includes new bioinformatic analyses to characterize the evolutionary origin of two G/T mismatch-specific thymine DNA glycosylases, MBD4 and TDG.

  7. Degradation of methyl orange photocatalyzed by polyoxometalate-intercalated layered double hydroxide%杂多酸阴离子[Co2Bi2W20O70]10-柱撑水滑石光催化降解甲基橙

    Institute of Scientific and Technical Information of China (English)

    彭芋杰; 许林

    2012-01-01

    采用离子交换法合成了一种新型的杂多酸阴离子[C02Bi2W20O70]10-柱撑水滑石类层状化合物,利用X射线衍射仪和傅立叶变换红外光谱仪分析了其晶相结构;研究了[Co2 Bi2W20O70]10柱撑水滑石光催化降解甲基橙的活性.结果表明,合成的[Co2B12W20O70]10-杂多酸阴离子柱撑水滑石较好地保持了水滑石原有的晶体形貌,具有较高的离子交换度.与此同时,杂多酸阴离子替换NO3后,可以在一定程度上提高催化剂的催化活性.这主要归因于水滑石材料中杂多酸阴离子和水滑石层板之间的协同效应.%Polyoxometalate-intercalated layered double hydroxide (POM-LDH) was obtained by aqueous ion exchange of a Zn-Al LDH precursor in nitrate. The crystalline structure of result-ant POM-LDH with polyoxometalate anion [Co2Bi2W20O70]10-was analyzed by means of X-ray diffraction and Fourier transform infrared spectrometry. It has been found that as-synthesized POM-LDH well retains the crystalline morphology of hydrotalcite and possesses a high ion ex-change capacity. In the meantime, the intercalation of large cluster anion [Co2 Bi2 W20 O70 ]10 into LDH contributes to increase the catalytic activity to the degradation to cationic dye methyl orange. This is mainly attributed to the synergistic effect between the polyoxometalate anion [Co2Bi2 W20O70]10- and the layered structure of the hydrotalcite.

  8. 板式纳米碳纤维负载二氧化钛光催化复合材料的制备及降解甲基橙的研究%Preparation of TiO2/Platelet Carbon Their Photocatalytic Performance for Nanofiber Nanocomposites and Degradation of Methyl Orange

    Institute of Scientific and Technical Information of China (English)

    因博; 龙东辉; 徐伟; 许胜; 乔文明; 凌立成

    2012-01-01

    Platelet nanofibers (PCNF) pretreated by acidity oxidation treatment was employed as supports to prepare TiOJPCNF nanocomposites by a hydrothermal process with titanium (IV) isopropoxide as the precursor, its photocatalysis activity and recycle property were investigated. The TiO2 content of photocatalysts was turned by changing the precursor. The pure PCNF and the composites were characterized by Nitrogen adsorption, XRD, TGDSC, SEM and Energy disperse spectroscopy, and TEM. The results showed that anatase TiO2 nanoparticles could be highly dispersed on the surface of fibers, leading to the formation of high performance photocatalysts for degradation of methyl orange (MO) under UV irradiation. The MC promoted the dispersion of TiO2 in composite system and induced synergistic effects of adsorption and phtocatalytic degradation on the removal of MO. The highest MO remove rate could reach as high as 80.1% in 120 min for different TiOz content samples and 79.2% for different temperature under UV irradiation. After three cycle reaction, the MO remove rate could still reach 80.0%.%以板式纳米碳纤维为载体,采用酸性氧化法对载体进行预处理之后,使用钛酸异丙酯为钛源,高温水热法制备了二氧化钛/纳米碳纤维复合光催化剂,并考察了其对甲基橙的光催化去除能力及循环反应性能.复合材料中二氧化钛含量通过改变前驱体组成进行调节.材料的结构性能通过氮气吸附、X射线衍射(XRD)、能谱分析仪(EDS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、热重分析仪(TG—DSC)等测试技术进行了表征.结果表明,锐钛矿型的二氧化钛以纳米颗粒形式均匀分散在纳米碳纤维表面,从而形成了高度分散的二氧化钛/碳纤维纳米复合材料.另外,复合系统中中孔吸附作用的存在,与纳米二氧化钛的光催化产生协同作用,增强了复合材料在紫外光照射下对于

  9. Research on preparation of iron doped TiO2-SBA-1 5 catalyst and photocatalytic degradation of methyl orange%铁掺杂TiO2-SBA-15催化剂制备及光催化降解甲基橙研究

    Institute of Scientific and Technical Information of China (English)

    徐玲; 王丽丽; 刘建华; 吕茂萍

    2016-01-01

    采用溶胶-凝胶法,将TiO2负载到介孔分子筛 SBA-15上,再通过 FeCl3浸渍的方法,将不同量的铁掺杂到TiO2-SBA-15上.通过 FT-IR、XRD、N2吸附-脱附和 TEM等手段对铁掺杂TiO2-SBA-15催化剂进行表征.结果表明:负载TiO2后的 SBA-15依然为高度有序的二维六方结构,比表面积略有减小,说明 SBA-15的孔道结构有利于 TiO2的分散.掺铁后的TiO2-SBA-15的结构改变不大,且TiO2晶形仍为锐钛矿型.最后以光催化降解甲基橙探究不同铁掺杂量的TiO2-SBA-15催化活性.结果表明:铁离子掺杂量为0.035%(质量分数),紫外光照射200 min时,甲基橙降解率达最高值98.2%.%By sol-gel method TiO2 is loaded on mesoporous molecular sieve SBA-1 5 .The catalysts which have different contents of iron,are obtained by impregnating FeCl3 onto TiO2-SBA-1 5 .The catalysts are characterized by FT-IR,XRD,N2 adsorption-desorption and TEM.The characterization results indicate that the TiO2 loaded SBA-1 5 still has highly ordered 2-dimensional hexagonal structure and the BET surface area is slightly decreased,which demonstrate that the channel of SBA-1 5 is beneficial to the scatter of the TiO2 .The structure of TiO2-SBA-1 5 has not changed too much after doping with iron.The crystalline form of TiO2 is still anatase.The catalytic activity of iron doped TiO2-SBA-15 is investigated by photocatalytic degradation of methyl orange.The photo-catalysis results reveal that when the doped content of iron is 0.035% (the mass fraction)and UV radiation time is 200 min,the degradation rate can reach maximum of 98.2%.

  10. The potential role of DNA methylation in the pathogenesis of abdominal aortic aneurysm.

    Science.gov (United States)

    Toghill, Bradley J; Saratzis, Athanasios; Harrison, Seamus C; Verissimo, Ana R; Mallon, Eamonn B; Bown, Matthew J

    2015-07-01

    Abdominal aortic aneurysm (AAA) is characterised by the chronic degradation and gradual, irreversible dilation of the abdominal aorta. Smoking, genetics, male sex and increased age are major factors associated with developing AAA. Rupture contributes to around 2% of deaths in all Caucasians over 65, and there is no pharmaco-therapeutic treatment. Methylation is an epigenetic modification to DNA, where a methyl group is added to a cytosine base 5' to a guanine (CpG dinucleotide). Methylation patterns are long term, inherited signatures that can induce changes in gene transcription, and can be affected by both genetic and environmental factors. Methylation changes are involved in hypertension and atherosclerosis, both of which are risk factors of, and often coexist with AAA. Extra-cellular matrix degradation and inflammation, both important pathological hallmarks of AAA, are also promoted by changes in CpG methylation in other diseases. Additionally, the adverse effects of smoking and ageing take place largely through epigenetic manipulation of the genome. Every factor associated with AAA appears to be associated with DNA methylation, yet no direct evidence confirms this. Future work to identify a link between global methylation and AAA, and differentially methylated regions may reveal valuable insight. The identification of a common epigenetic switching process may also signify a promising future for AAA pharmaco-therapeutic strategies. Epigenetic therapies are being designed to target pathogenic CpG methylation changes in other diseases, and it is feasible that these therapies may also be applicable to AAA in the future.

  11. Methylated β-Cyclodextrins

    DEFF Research Database (Denmark)

    Schönbeck, Jens Christian Sidney; Westh, Peter; Madsen, Jens Christian

    2011-01-01

    groups at O2 promote complexation by extending the hydrophobic cavity. Like in the case of 2-hydroxypropylated cyclodextrins, the methyl substituents cause an increased release of ordered water from the hydration shell of the bile salts, resulting in a strong increase in both the enthalpy and the entropy...

  12. Methylated β-Cyclodextrins

    DEFF Research Database (Denmark)

    Schönbeck, Jens Christian Sidney; Westh, Peter; Madsen, Jens Christian

    2011-01-01

    groups at O2 promote complexation by extending the hydrophobic cavity. Like in the case of 2-hydroxypropylated cyclodextrins, the methyl substituents cause an increased release of ordered water from the hydration shell of the bile salts, resulting in a strong increase in both the enthalpy and the entropy...

  13. Architecture and spatial organization in a triple-species bacterial biofilm synergistically degrading the phenylurea herbicide linuron

    DEFF Research Database (Denmark)

    Breugelmans, Philip; Barken, Kim Bundvig; Tolker-Nielsen, Tim;

    2008-01-01

    Members of a triple-species 3-(3,4-dichlorophenyl)-1-methoxy-1-methyl urea (linuron)-mineralizing consortium, i.e. the linuron- and 3,4-dichloroaniline-degrading Variovorax sp. WDL1, the 3,4-dichloroaniline-degrading Comamonas testosteroni WDL7 and the N,O-dimethylhydroxylamine-degrading Hyphomic...

  14. O-Methyl cyclolaudenol

    Directory of Open Access Journals (Sweden)

    Nisar Hussain

    2009-06-01

    Full Text Available The title compound (systematic name: 3-methoxy-24-methyl-9,19-cyclolanost-25-ene, C32H54O, is a triterpenoid which has been isolated from Skimmia laureola. The three six-membered rings adopt chair, slightly distorted half-chair and distorted boat conformations, and the five-membered ring adopts an envelope conformation. All the rings are trans fused.

  15. Kaempferol Modulates DNA Methylation and Downregulates DNMT3B in Bladder Cancer

    Directory of Open Access Journals (Sweden)

    Wei Qiu

    2017-03-01

    Full Text Available Background: Genomic DNA methylation plays an important role in both the occurrence and development of bladder cancer. Kaempferol (Kae, a natural flavonoid that is present in many fruits and vegetables, exhibits potent anti-cancer effects in bladder cancer. Similar to other flavonoids, Kae possesses a flavan nucleus in its structure. This structure was reported to inhibit DNA methylation by suppressing DNA methyltransferases (DNMTs. However, whether Kae can inhibit DNA methylation remains unclear. Methods: Nude mice bearing bladder cancer were treated with Kae for 31 days. The genomic DNA was extracted from xenografts and the methylation changes was determined using an Illumina Infinium HumanMethylation 450 BeadChip Array. The ubiquitination was detected using immuno-precipitation assay. Results: Our data indicated that Kae modulated DNA methylation in bladder cancer, inducing 103 differential DNA methylation positions (dDMPs associated with genes (50 hyper-methylated and 53 hypo-methylated. DNA methylation is mostly relied on the levels of DNMTs. We observed that Kae specifically inhibited the protein levels of DNMT3B without altering the expression of DNMT1 or DNMT3A. However, Kae did not downregulate the transcription of DNMT3B. Interestingly, we observed that Kae induced a premature degradation of DNMT3B by inhibiting protein synthesis with cycloheximide (CHX. By blocking proteasome with MG132, we observed that Kae induced an increased ubiquitination of DNMT3B. These results suggested that Kae could induce the degradation of DNMT3B through ubiquitin-proteasome pathway. Conclusion: Our data indicated that Kae is a novel DNMT3B inhibitor, which may promote the degradation of DNMT3B in bladder cancer.

  16. Sinalbin degradation products in mild yellow mustard paste

    Directory of Open Access Journals (Sweden)

    Paunović Dragana

    2012-01-01

    Full Text Available Sinalbin degradation products in mild yellow mustard paste were investigated. The analyzed material consisted of a mild yellow mustard paste condiment and ground white mustard seeds which were originally used in the mustard paste production process. The samples were extracted in a Soxhlet extraction system and analyzed by gas chromatography - mass spectrometry (GC-MS technique. The only sinalbin degradation product in ground mustard seeds was 2-(4-hydroxyphenylacetonitrile. The most abundant sinalbin degradation product in yellow mustard paste was 4-(hydroxymethylphenol. Other compounds identified in this sample were: 4-methyl phenol, 4-ethyl phenol, 4-(2-hydroxyethylphenol and 2-(4-hydroxyphenyl ethanoic acid.

  17. Degradation of aromatic compounds and degradative pathway of 4-nitrocatechol by Ochrobactrum sp. B2.

    Science.gov (United States)

    Zhong, Qiuzan; Zhang, Haiyan; Bai, Wenqin; Li, Mei; Li, Baotong; Qiu, Xinghui

    2007-12-01

    The potential capacity of a soil methyl parathion-degrading bacterium strain, Ochrobactrum sp. B2, for degrading various aromatic compounds were investigated. The results showed B2 was capable of degrading diverse aromatic compounds, but amino-substituted benzene compounds, at a concentration up to 100 mg L(-1) in 4 days. B2 could use 4-nitrocatechol (4-NC) as a sole carbon and energy source with release of nitrite ion. The pathway for 4-NC degradation via 1,2,4-benzenetriol (BT) and hydroquinone (HQ) formation in B2 was proposed based on the identification and quantification of intermediates by gas chromatography-mass spectrometry (GC-MS), and high performance liquid chromatography (HPLC). Degradation studies carried out on a plasmid-cured derivative showed that the genes for 4-NC degradative pathway was plasmid-borne in B2, suggesting that B2 degrades both p-nitrophenol and 4-NC by enzymes encoded by genes on the same plasmid.

  18. Bound 14C-metsulfuron-methyl residue in soils

    Institute of Scientific and Technical Information of China (English)

    YE Qing-fu; DING Wei; WANG Hai-yan; HAN Ai-liang; SUN Jin-he

    2005-01-01

    Bound residue(BR) of 14 C-metsulfuron-methyl (14 C-BR) in seven kinds of soil was significantly negative-related to soil pH and positive-related to the clay content during the initial 20 d of incubation, but only was significantly negative-related to soil pH after 30 d incubation. Again, the soil pH was found to be the dominant factor affecting BR formation from 14 C-metsulfuron-methyl among the basic properties(soil pH, clay, OM and CEC etc.) of soil. The maximum content of 14C-BR in the 7 soils accounted for 19.3% -52.6% of applied amount. In addition, the composition of the 14 C-BR in fluvio marine yellow loamy(S7 ) at the 90 d of incubation was identified using the coupling technique of LC-MS and isotope tracing method. The results showed that the 14 C-[2-amino-4-hydroxyl-6-methyl-1, 3, 5]-triazine, 14 C-[2-amino-4-methoxy-6-methyl-1, 3, 5]-triazine and 14 C-metsulfuron-methyl parent compound constituted the main components of the BR derived from 14 C-metsulfuron-methyl in the S7. The relative percentage of the three compounds accounted for 41.4 %, 35.8 % and 19.3 % of total recovery radioactivity, respectively. The results also indicated that a non- radioactive component, 2-methylformate-benzenesulfonyl-isocyanate, one of the degraded products of metsulfuron-methyl in soil, was also found to be one of the components of the BR. The parent compound in BR can well explain the phytotoxic effect on substitution crops caused by the BR derived from metsulfuron-methyl in soil.

  19. Methylation in hepatocellular carcinoma

    Directory of Open Access Journals (Sweden)

    Regina M. Santella

    2007-02-01

    Full Text Available

    The development of HCC is a complex, multistep, multistage process. The molecular pathogenesis of HCC appears to involve multiple genetic aberrations in the molecular control of hepatocyte proliferation, differentiation and death and the maintenance of genomic integrity. This process is influenced by the cumulative activation and inactivation of oncogenes, tumor suppressor genes and other genes. p53, a tumor suppressor gene, is the most frequently mutated gene in human cancers. There is also a striking sequence specific binding and induction of mutations by AFB1 at codon 249 of p53 in HCC.

    Epigenetic alterations are also involved in cancer development and progression. Methylation of promoter CpG islands is associated with inhibition of transcriptional initiation and permanent silencing of downstream genes.

    It is now known that most important tumor suppressor genes are inactivated, not only by mutations and deletions but also by promoter methylation. Several studies indicated that p16, p15, RASSF1A, MGMT, and GSTP1 promoter hypermethylation are prevalent in HCC. In addition, geographic variation in the methylation status of tumor DNA indicates that environmental factors may influence the frequent and concordant degree of hypermethylation in multiple genes in HCC and that epigeneticenvironmental interactions may be involved in hepatocarcinogenesis. We have found significant relationships between promoter methylation and AFB1-DNA adducts confirming the impact of environmental exposures on gene methylation.

    DNA isolated from serum or plasma of cancer patients frequently contains the same genetic and

  20. PEM fuel cell degradation

    Energy Technology Data Exchange (ETDEWEB)

    Borup, Rodney L [Los Alamos National Laboratory; Mukundan, Rangachary [Los Alamos National Laboratory

    2010-01-01

    The durability of PEM fuel cells is a major barrier to the commercialization of these systems for stationary and transportation power applications. While significant progress has been made in understanding degradation mechanisms and improving materials, further improvements in durability are required to meet commercialization targets. Catalyst and electrode durability remains a primary degradation mode, with much work reported on understanding how the catalyst and electrode structure degrades. Accelerated Stress Tests (ASTs) are used to rapidly evaluate component degradation, however the results are sometimes easy, and other times difficult to correlate. Tests that were developed to accelerate degradation of single components are shown to also affect other component's degradation modes. Non-ideal examples of this include ASTs examining catalyst degradation performances losses due to catalyst degradation do not always well correlate with catalyst surface area and also lead to losses in mass transport.

  1. Methylation profiling using methylated DNA immunoprecipitation and tiling array hybridization.

    Science.gov (United States)

    Cheung, Hoi-Hung; Lee, Tin-Lap; Rennert, Owen M; Chan, Wai-Yee

    2012-01-01

    DNA methylation is an important epigenetic modification that regulates development and plays a role in the pathophysiology of many diseases. It is dynamically changed during germline development. Methylated DNA immunoprecipitation (MeDIP) is an efficient, cost-effective method for locus-specific and genome-wide analysis. Methylated DNA fragments are enriched by a 5-methylcytidine-recognizing antibody, therefore allowing the analysis of both CpG and non-CpG methylation. The enriched DNA fragments can be amplified and hybridized to tiling arrays covering CpG islands, promoters, or the entire genome. Comparison of different methylomes permits the discovery of differentially methylated regions that might be important in disease- or tissue-specific expression. Here, we describe an established MeDIP protocol and tiling array hybridization method for profiling methylation of testicular germ cells.

  2. Event extraction for DNA methylation

    Directory of Open Access Journals (Sweden)

    Ohta Tomoko

    2011-10-01

    Full Text Available Abstract Background We consider the task of automatically extracting DNA methylation events from the biomedical domain literature. DNA methylation is a key mechanism of epigenetic control of gene expression and implicated in many cancers, but there has been little study of automatic information extraction for DNA methylation. Results We present an annotation scheme for DNA methylation following the representation of the BioNLP shared task on event extraction, select a set of 200 abstracts including a representative sample of all PubMed citations relevant to DNA methylation, and introduce manual annotation for this corpus marking nearly 3000 gene/protein mentions and 1500 DNA methylation and demethylation events. We retrain a state-of-the-art event extraction system on the corpus and find that automatic extraction of DNA methylation events, the methylated genes, and their methylation sites can be performed at 78% precision and 76% recall. Conclusions Our results demonstrate that reliable extraction methods for DNA methylation events can be created through corpus annotation and straightforward retraining of a general event extraction system. The introduced resources are freely available for use in research from the GENIA project homepage http://www-tsujii.is.s.u-tokyo.ac.jp/GENIA.

  3. Inhibitors and pathways of hepatocytic protein degradation.

    Science.gov (United States)

    Seglen, P O; Gordon, P B; Grinde, B; Solheim, A; Kovács, A L; Poli, A

    1981-01-01

    On the basis of experiments using amino acids and various inhibitors (lysosomotropic amines, leupeptin, chymostatin, vanadate, vinblastine, anoxia, methylaminopurines), five different modes of endogenous protein degradation in isolated rat hepatocytes can be distinguished. The two non-lysosomal (amine-resistant) mechanisms preferentially degrade relatively labile (short-lived) proteins: one of these mechanisms is energy-dependent and chymostatin-sensitive, the other is not. Of the three lysosomal (amine-sensitive) mechanisms, one--quantitatively minor--is amino acid-resistant and preferentially degrades labile proteins. The two amino acid-sensitive mechanisms each seen account for about one-half of the degradation of relatively stable (long-lived) proteins; one of them is suppressed by leucine and apparently corresponds to the formation of electron microscopically visible autophagosomes; the other may represent a different type of autophagy, inhibited by asparagine and glutamine. A new class of inhibitors, the purine derivatives (methylated 6-aminopurines, and 6-mercaptopurines) appear to specifically suppress autophagic/lysosomal protein degradation, and may help to further elucidate the mechanisms of autophagy.

  4. 可见光下掺N附Ag纳米TiO2的光催化降解甲基橙%Photocatalytic degradation of methyl orange by N-doped and Ag-loaded nano-TiO2 under visible light

    Institute of Scientific and Technical Information of China (English)

    张鹏飞; 李晓维; 伍兴科

    2016-01-01

    electron and hole, so that it can promote the visible absorbance of TiO2. Ag0 loaded on TiO2 barely affects lattice parameters of TiO2, but significantly results in a strong surface plasmon absorbance band in the visible region of 450−580 nm, which can extend to near infrared region. The degradation rate is in the order of Ag/N-TiO2>Ag/TiO2>N-TiO2>TiO2(or Degussa P25). The degradation rate of methyl orange (MO) can reach 95% after visible light irradiation over Ag/N-TiO2 for 150 min.

  5. Sonolytic degradation of dimethoate: kinetics, mechanisms and toxic intermediates controlling.

    Science.gov (United States)

    Yao, Juan-Juan; Hoffmann, Michael R; Gao, Nai-Yun; Zhang, Zhi; Li, Lei

    2011-11-15

    The sonolytic degradation of aqueous solutions of dimethoate, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl]dithiophosphate, was examined. Optimal degradation rates were obtained at 619 kHz for continuous sonolysis and 406 kHz for pulse sonolysis. The primary pathways for degradation include hydroxyl radical oxidation, hydrolysis and pyrolysis on collapsing cavitation bubble interfaces. Reaction mechanisms coupled with the corresponding kinetic models are proposed to reproduce the observed concentration versus time profiles for dimethoate, omethoate and N-(methyl) mercaptoacetamide during sonolysis. The oxidation and hydrolysis of dimethoate and omethoate occurred at the water-bubble interface was the rate-determining step for sonolytic overall degradation of dimethoate. More than 90% toxicity of dimethoate was reduced within 45 min ultrasonic irradiation. Ferrous ion at micro molar level can significantly enhance the sonolytic degradation of dimethoate and effectively reduce the yields of toxic intermediate omethoate.

  6. Degradation of microbial polyesters.

    Science.gov (United States)

    Tokiwa, Yutaka; Calabia, Buenaventurada P

    2004-08-01

    Microbial polyhydroxyalkanoates (PHAs), one of the largest groups of thermoplastic polyesters are receiving much attention as biodegradable substitutes for non-degradable plastics. Poly(D-3-hydroxybutyrate) (PHB) is the most ubiquitous and most intensively studied PHA. Microorganisms degrading these polyesters are widely distributed in various environments. Although various PHB-degrading microorganisms and PHB depolymerases have been studied and characterized, there are still many groups of microorganisms and enzymes with varying properties awaiting various applications. Distributions of PHB-degrading microorganisms, factors affecting the biodegradability of PHB, and microbial and enzymatic degradation of PHB are discussed in this review. We also propose an application of a new isolated, thermophilic PHB-degrading microorganism, Streptomyces strain MG, for producing pure monomers of PHA and useful chemicals, including D-3-hydroxycarboxylic acids such as D-3-hydroxybutyric acid, by enzymatic degradation of PHB.

  7. [Monitoring the sewage degradation by analyzing optic fiber SPR spectrum character].

    Science.gov (United States)

    Zhang, Xiao-Li; Liang, Da-Kai; Zeng, Jie; Zhao, Zhi-Yuan; Zeng, Jian-Min

    2010-02-01

    The working principle of the optic fiber SPR sensor was discussed in the present paper at first. The feasibility of using it to monitor the degradation process of the environmental sewage represented by the methyl orange was studied. Finally, the optic fiber SPR sensor was adopted to monitor the change in degradation concentration represented by the original methyl orange solution on the base of 50 mL initial concentration 30 mg x L(-1), and the optic fiber SPR spectrum character of degradation process was analyzed in detail. Meanwhile the UV spectrophotometer was used to measure the change in concentration in the course of the degradation. The measurement data were analyzed and compared at large. The research work indicates that both the methods have consistent results, as the degradation time increases, the absorbance and concentration of the environmental sewage represented by the methyl orange solution decrease by and by, and the resonant wavelength of the optic fiber SPR sensor blue shifts step by step, as compared to the original standardization methyl orange solution resonant spectrum. It was shown that the methyl orange solution was degraded, and the rate of degradation was up to about 73 percent within two hours. The comparative results illustrate that it is feasible to use the optic fiber SPR sensor to monitor the environmental sewage degradation. The research result not only provides a new monitoring method for the degradation process of the environmental sewage, but also promotes the technique of the SPR sensor combined to the environment monitor by a long way.

  8. DNA methylation in metabolic disorders

    DEFF Research Database (Denmark)

    Barres, Romain; Zierath, Juleen R

    2011-01-01

    DNA methylation is a major epigenetic modification that controls gene expression in physiologic and pathologic states. Metabolic diseases such as diabetes and obesity are associated with profound alterations in gene expression that are caused by genetic and environmental factors. Recent reports...... have provided evidence that environmental factors at all ages could modify DNA methylation in somatic tissues, which suggests that DNA methylation is a more dynamic process than previously appreciated. Because of the importance of lifestyle factors in metabolic disorders, DNA methylation provides...... a mechanism by which environmental factors, including diet and exercise, can modify genetic predisposition to disease. This article considers the current evidence that defines a role for DNA methylation in metabolic disorders....

  9. DNA Methylation in Schizophrenia.

    Science.gov (United States)

    Pries, Lotta-Katrin; Gülöksüz, Sinan; Kenis, Gunter

    2017-01-01

    Schizophrenia is a highly heritable psychiatric condition that displays a complex phenotype. A multitude of genetic susceptibility loci have now been identified, but these fail to explain the high heritability estimates of schizophrenia. In addition, epidemiologically relevant environmental risk factors for schizophrenia may lead to permanent changes in brain function. In conjunction with genetic liability, these environmental risk factors-likely through epigenetic mechanisms-may give rise to schizophrenia, a clinical syndrome characterized by florid psychotic symptoms and moderate to severe cognitive impairment. These pathophysiological features point to the involvement of epigenetic processes. Recently, a wave of studies examining aberrant DNA modifications in schizophrenia was published. This chapter aims to comprehensively review the current findings, from both candidate gene studies and genome-wide approaches, on DNA methylation changes in schizophrenia.

  10. DNA methylation and carcinogenesis.

    Science.gov (United States)

    Lichtenstein, A V; Kisseljova, N P

    2001-03-01

    In the world of easy things truth is opposed to lie; in the world of complicated things one profound truth is opposed to another not less profound than the first. Neils Bohr The hypothesis of the exclusively genetic origin of cancer ("cancer is a disease of genes, a tumor without any damage to the genome does not exist") dominated in the oncology until recently. A considerable amount of data confirming this hypothesis was accumulated during the last quarter of the last century. It was demonstrated that the accumulation of damage of specific genes lies at the origin of a tumor and its following progression. The damage gives rise to structural changes in the respective proteins and, consequently, to inappropriate mitogenic stimulation of cells (activation of oncogenes) or to the inactivation of tumor suppressor genes that inhibit cell division, or to the combination of both (in most cases). According to an alternative (epigenetic) hypothesis that was extremely unpopular until recently, a tumor is caused not by a gene damage, but by an inappropriate function of genes ("cancer is a disease of gene regulation and differentiation"). However, recent studies led to the convergence of these hypotheses that initially seemed to be contradictory. It was established that both factors--genetic and epigenetic--lie at the origin of carcinogenesis. The relative contribution of each varies significantly in different human tumors. Suppressor genes and genes of repair are inactivated in tumors due to their damage or methylation of their promoters (in the latter case an "epimutation", an epigenetic equivalent of a mutation, occurs, producing the same functional consequences). It is becoming evident that not only the mutagens, but various factors influencing cell metabolism, notably methylation, should be considered as carcinogens.

  11. DNA Methylation in Thyroid Tumorigenesis

    Energy Technology Data Exchange (ETDEWEB)

    Stephen, Josena K., E-mail: jstephe2@hfhs.org [Department of Otolaryngology/Head and Neck Surgery, Henry Ford Hospital, Detroit, MI 48202 (United States); Chitale, Dhananjay [Department of Pathology, Henry Ford Hospital, Detroit, MI 48202 (United States); Narra, Vinod [Essex Surgical Associates, PC, Beverly, MA 01915 (United States); Chen, Kang Mei; Sawhney, Raja; Worsham, Maria J. [Department of Otolaryngology/Head and Neck Surgery, Henry Ford Hospital, Detroit, MI 48202 (United States)

    2011-03-29

    Thyroid cancer is the most common endocrine cancer with 1,690 deaths each year. There are four main types of which the papillary and follicular types together account for >90% followed by medullary cancers with 3% to 5% and anaplastic carcinomas making up <3%. Epigenetic events of DNA hypermethylation are emerging as promising molecular targets for cancer detection. Our immediate and long term goal is to identify DNA methylation markers for early detection of thyroid cancer. This pilot study comprised of 21 patients to include 11 papillary thyroid cancers (PTC), 2 follicular thyroid cancers (FTC), 5 normal thyroid cases, and 3 hyperthyroid cases. Aberrant promoter methylation was examined in 24 tumor suppressor genes using the methylation specific multiplex ligation-dependent probe amplification (MS-MLPA) assay and in the NIS gene using methylation-specific PCR (MSP). The frequently methylated genes were CASP8 (17/21), RASSF1 (16/21) and NIS (9/21). In the normal samples, CASP8, RASSF1 and NIS were methylated in 5/5, 4/5 and 1/5 respectively. In the hyperthyroid samples, CASP8, RASSF1 and NIS were methylated in 3/3, 2/3 and 1/3 respectively. In the thyroid cancers, CASP8, RASSF1, and NIS were methylated in 9/13, 10/13, and 7/13 respectively. CASP8, RASSF1 and NIS were also methylated in concurrently present normal thyroid tissue in 3/11, 4/11 and 3/11 matched thyroid cancer cases (matched for presence of both normal thyroid tissue and thyroid cancer), respectively. Our data suggests that aberrant methylation of CASP8, RASSF1, and NIS maybe an early change in thyroid tumorigenesis regardless of cell type.

  12. Bacterial Degradation of Pesticides

    DEFF Research Database (Denmark)

    Knudsen, Berith Elkær

    . Bioaugmentation i.e. addition of specific degrader organisms, has been suggested as an environmentally friendly and economically competitive strategy for cleaning polluted sites. Several organisms have been isolated, capable of degrading different compounds. However the capacity to degrade the desired compound...... SRS2, Variovorax SRS16 and Arthrobacter globiformis D47. The degradation capacity of each strain individually as well as two- and three-member consortia was studied in a sand column set up. Glass beads were added to the set up to create a dry patch, separating the organisms and the diuron-spiked sand...

  13. Degradation of phenazone in aqueous solution with ozone: influencing factors and degradation pathways.

    Science.gov (United States)

    Miao, Heng-Feng; Cao, Meng; Xu, Dan-Yao; Ren, Hong-Yan; Zhao, Ming-Xing; Huang, Zhen-Xing; Ruan, Wen-Quan

    2015-01-01

    Oxidation kinetics and degradation pathways of phenazone (an analgesic and antipyretic drug) upon reaction with O3 were investigated. Kinetic studies on degradation of phenazone were carried out under different operating conditions such as temperature, pH, anions and H2O2 addition. Results showed that the degradation followed the pseudo-first-order kinetic model. The reaction rate constant (kobs) of phenazone reached the maximum at 20 °C (9.653×10(-3) s(-1)). The presence of NO3(-) could enhance the degradation rate, while the addition of HCO3(-), SO4(2)(-), Cl(-) and the rise of pH showed negative effects on the ozonation of phenazone. H2O2 addition increased the phenazone degradation efficiency by 45.9% with the optimal concentration of 0.135 mM. Reaction by-products were evaluated by UPLC-Q-TOF-MS, which allowed the identification of a total of 10 by-products. The transformation pathways of phenazone ozonation consisted mainly of electrophilic addition and substitution, pyrazole ring opening, hydroxylation, dephenylization and coupling. The toxicity of these intermediate products showed that they are expected not to be more toxic than phenazone, with the exception of P7 (aniline) and P10 (1,5-dimethyl-4-((1-methyl-2-phenylhydrazinyl)methoxy)-2-phenyl-1H-pyrazol-3(2H)-one).

  14. Batteries: Imaging degradation

    Science.gov (United States)

    Shearing, Paul R.

    2016-11-01

    The degradation and failure of Li-ion batteries is strongly associated with electrode microstructure change upon (de)lithiation. Now, an operando X-ray tomography approach is shown to correlate changes in the microstructure of electrodes to cell performance, and thereby predict degradation pathways.

  15. Syntrophy in Methanogenic Degradation

    NARCIS (Netherlands)

    Worm, P.; Müller, N.; Plugge, C.M.; Stams, A.J.M.; Schink, B.

    2010-01-01

    This chapter deals with microbial communities of bacteria and archaea that closely cooperate in methanogenic degradation and perform metabolic functions in this community that neither one of them could carry out alone. The methanogenic degradation of fatty acids, alcohols, most aromatic compounds, a

  16. Rate of NDF degradation

    DEFF Research Database (Denmark)

    Weisbjerg, Martin Riis; Koukolová, V; Lund, Peter

    2007-01-01

    Degradation profiles for NDF were estimated for 83 samples of grass/grass-clover, 27 samples of cereal whole crop and 14 samples of maize whole crop.......Degradation profiles for NDF were estimated for 83 samples of grass/grass-clover, 27 samples of cereal whole crop and 14 samples of maize whole crop....

  17. Methylation-Specific PCR Unraveled

    Directory of Open Access Journals (Sweden)

    Sarah Derks

    2004-01-01

    Full Text Available Methylation‐specific PCR (MSP is a simple, quick and cost‐effective method to analyze the DNA methylation status of virtually any group of CpG sites within a CpG island. The technique comprises two parts: (1 sodium bisulfite conversion of unmethylated cytosine's to uracil under conditions whereby methylated cytosines remains unchanged and (2 detection of the bisulfite induced sequence differences by PCR using specific primer sets for both unmethylated and methylated DNA. This review discusses the critical parameters of MSP and presents an overview of the available MSP variants and the (clinical applications.

  18. Bisulfite Conversion of DNA: Performance Comparison of Different Kits and Methylation Quantitation of Epigenetic Biomarkers that Have the Potential to Be Used in Non-Invasive Prenatal Testing.

    Directory of Open Access Journals (Sweden)

    Chrysanthia A Leontiou

    Full Text Available Epigenetic alterations, including DNA methylation, play an important role in the regulation of gene expression. Several methods exist for evaluating DNA methylation, but bisulfite sequencing remains the gold standard by which base-pair resolution of CpG methylation is achieved. The challenge of the method is that the desired outcome (conversion of unmethylated cytosines positively correlates with the undesired side effects (DNA degradation and inappropriate conversion, thus several commercial kits try to adjust a balance between the two. The aim of this study was to compare the performance of four bisulfite conversion kits [Premium Bisulfite kit (Diagenode, EpiTect Bisulfite kit (Qiagen, MethylEdge Bisulfite Conversion System (Promega and BisulFlash DNA Modification kit (Epigentek] regarding conversion efficiency, DNA degradation and conversion specificity.Performance was tested by combining fully methylated and fully unmethylated λ-DNA controls in a series of spikes by means of Sanger sequencing (0%, 25%, 50% and 100% methylated spikes and Next-Generation Sequencing (0%, 3%, 5%, 7%, 10%, 25%, 50% and 100% methylated spikes. We also studied the methylation status of two of our previously published differentially methylated regions (DMRs at base resolution by using spikes of chorionic villus sample in whole blood.The kits studied showed different but comparable results regarding DNA degradation, conversion efficiency and conversion specificity. However, the best performance was observed with the MethylEdge Bisulfite Conversion System (Promega followed by the Premium Bisulfite kit (Diagenode. The DMRs, EP6 and EP10, were confirmed to be hypermethylated in the CVS and hypomethylated in whole blood.Our findings indicate that the MethylEdge Bisulfite Conversion System (Promega was shown to have the best performance among the kits. In addition, the methylation level of two of our DMRs, EP6 and EP10, was confirmed. Finally, we showed that bisulfite

  19. The thermal degradation of poly(iso-butyl methacrylate and poly(sec-butyl methacrylate

    Directory of Open Access Journals (Sweden)

    IVANKA G. POPOVIC

    2000-12-01

    Full Text Available The non-oxidative thermal degradation of poly(iso-butyl methacrylate and poly(sec-butyl methacrylate was investigated by studying changes in the polymer residue. Due to the different number of b-hydrogens in their ester substituents, these two polymeric isomers behave differently when subjected to elevated temperatures. Poly(iso-butyl methacrylate degrades quantitatively by depolymerisation with zip lengths of the same order of magnitude as those of poly(methyl methacrylate. Poly(sec-butyl methacrylate degrades by a combined degradation mechanism of depolymerisation and de-esterification. De-esterification becomes a significant thermolysis route at temperatures higher than 240°C.

  20. Intermittent degradation and schizotypy

    Directory of Open Access Journals (Sweden)

    Matthew W. Roché

    2015-06-01

    Full Text Available Intermittent degradation refers to transient detrimental disruptions in task performance. This phenomenon has been repeatedly observed in the performance data of patients with schizophrenia. Whether intermittent degradation is a feature of the liability for schizophrenia (i.e., schizotypy is an open question. Further, the specificity of intermittent degradation to schizotypy has yet to be investigated. To address these questions, 92 undergraduate participants completed a battery of self-report questionnaires assessing schizotypy and psychological state variables (e.g., anxiety, depression, and their reaction times were recorded as they did so. Intermittent degradation was defined as the number of times a subject’s reaction time for questionnaire items met or exceeded three standard deviations from his or her mean reaction time after controlling for each item’s information processing load. Intermittent degradation scores were correlated with questionnaire scores. Our results indicate that intermittent degradation is associated with total scores on measures of positive and disorganized schizotypy, but unrelated to total scores on measures of negative schizotypy and psychological state variables. Intermittent degradation is interpreted as potentially derivative of schizotypy and a candidate endophenotypic marker worthy of continued research.

  1. Silk structure and degradation.

    Science.gov (United States)

    Liu, Bin; Song, Yu-wei; Jin, Li; Wang, Zhi-jian; Pu, De-yong; Lin, Shao-qiang; Zhou, Chan; You, Hua-jian; Ma, Yan; Li, Jin-min; Yang, Li; Sung, K L Paul; Zhang, Yao-guang

    2015-07-01

    To investigate the structure of silk and its degradation properties, we have monitored the structure of silk using scanning electron microscopy and frozen sections. Raw silk and degummed raw silk were immersed in four types of degradation solutions for 156 d to observe their degradation properties. The subcutaneous implants in rats were removed after 7, 14, 56, 84, 129, and 145 d for frozen sectioning and subsequent staining with hematoxylin and eosin (H.E.), DAPI, Beta-actin and Collagen I immunofluorescence staining. The in vitro weight loss ratio of raw silk and degummed raw silk in water, PBS, DMEM and DMEM containing 10% FBS (F-DMEM) were, respectively, 14%/11%, 12.5%/12.9%, 11.1%/14.3%, 8.8%/11.6%. Silk began to degrade after 7 d subcutaneous implantation and after 145 d non-degraded silk was still observed. These findings suggest the immunogenicity of fibroin and sericin had no essential difference. In the process of in vitro degradation of silk, the role of the enzyme is not significant. The in vivo degradation of silk is related to phagocytotic activity and fibroblasts may be involved in this process to secrete collagen. This study also shows the developing process of cocoons and raw silk.

  2. Optimization of atmospheric air plasma for degradation of organic dyes in wastewater.

    Science.gov (United States)

    Sarangapani, Chaitanya; Dixit, Y; Milosavljevic, Vladimir; Bourke, Paula; Sullivan, Carl; Cullen, P J

    2017-01-01

    This study optimises the degradation of a cocktail of the dyes methyl orange and bromothymol blue by atmospheric air plasma. Response surface methodology (RSM) was employed to investigate the efficacy of the plasma process parameters on degradation efficiency. A Box-Behnken design (BBD) was employed to optimise the degradation of dyes by air plasma discharge. A second order polynomial equation was proposed to predict process efficiency. It was observed that the predicted values are significant (p degradation, pH value and ozone concentration, respectively. The analysis of variance results showed that the coefficients of the polynomials for the percentage degradation and ozone concentration responses indicated positive linear effects (p degradation efficiencies are achieved with an increase in treatment duration. This study showed that a BBD model and RSM could be employed to optimize the colour degradation parameters of non-thermal plasma treated model dyes while minimising the number of experiments required.

  3. Behavior of Thiophanate Methyl and Propiconazole in Grape and Mango Fruits Under the Egyptian Field Conditions.

    Science.gov (United States)

    Soliman, Amira Sh; Helmy, Rania M A; Nasr, Islam N; Abbas, Mohamed S; Mahmoud, Hend A; Jiang, Wayne

    2017-05-01

    This research aims at determining residues of thiophanate methyl and propiconazole in grape and mango fruits as an indication for their persistence in this environmental compartment. Fruit extracts were analyzed for thiophanate methyl using High Performance Liquid Chromatography and using Gas Chromatography Electron Capture Detector (GC/ECD), respectively. The results indicated that propiconazole had a less environmental impact since propiconazole had shorter residue half-lives which were 1.24 and 1.19 days in grape and mango fruits, respectively, while thiophanate methyl had half-lives of 2.49 and 2.64 days in mango and grape, respectively. The degradation rates of propiconazole in grape and mango fruits did not change significantly and neither did those of thiophanate methyl. According to the maximum residue level, the pre-harvest intervals of propiconazole were set to be 3 and 7 days for grape and mango fruits, respectively, and the pre-harvest intervals for thiophanate methyl were 15 days for both grape and mango fruits. Propiconazole was generally considered to be less hazardous to humans and will leave the environment less altered because of its faster degradation than that of thiophanate methyl.

  4. Metal Complexation Studies of 1-(4-Carboxy-3-hydroxy-N-methyl phenyl- amino methyl 2-methyl perimidine

    Directory of Open Access Journals (Sweden)

    Umang N. Patel

    2009-01-01

    Full Text Available Aminomethylation of 2-methyl perimidine was carried out by treating 2-methyl perimidine with formaldehyde and 4-aminosalicylic acid. The resultant compound was designed as 1-(4-caroxy-3-hydroxy-N-methyl phenylamino methyl2-methyl perimidine. The transition metal complexes of Cu2+, Co2+, Ni2+, Mn2+ and Zn2+ have been prepared and characterized by elemental analysis, spectral studies, magnetic moment determination, molar conductivity measurement and antimicrobial activity.

  5. Cigarette smoking and DNA methylation

    Science.gov (United States)

    Lee, Ken W. K.; Pausova, Zdenka

    2013-01-01

    DNA methylation is the most studied epigenetic modification, capable of controlling gene expression in the contexts of normal traits or diseases. It is highly dynamic during early embryogenesis and remains relatively stable throughout life, and such patterns are intricately related to human development. DNA methylation is a quantitative trait determined by a complex interplay of genetic and environmental factors. Genetic variants at a specific locus can influence both regional and distant DNA methylation. The environment can have varying effects on DNA methylation depending on when the exposure occurs, such as during prenatal life or during adulthood. In particular, cigarette smoking in the context of both current smoking and prenatal exposure is a strong modifier of DNA methylation. Epigenome-wide association studies have uncovered candidate genes associated with cigarette smoking that have biologically relevant functions in the etiology of smoking-related diseases. As such, DNA methylation is a potential mechanistic link between current smoking and cancer, as well as prenatal cigarette-smoke exposure and the development of adult chronic diseases. PMID:23882278

  6. SPECIFIC DEGRADATION OF WATERSHEDS

    Institute of Scientific and Technical Information of China (English)

    Boubacar KANE; Pierre Y.JULIEN

    2007-01-01

    An extensive database of reservoir sedimentation surveys throughout continental United States is compiled and analyzed to determine specific degradation SD relationships as function of mean annual rainfall R, drainage area A, and watershed slope S. The database contains 1463 field measurements and specific degradation relationships are defined as function of A, R and S. Weak trends and significant variability in the data are noticeable. Specific degradation measurements are log normally distributed with respect to R, A, and S and 95% confidence intervals are determined accordingly. The accuracy of the predictions does not significantly increase as more independent variables are added to the regression analyses.

  7. Construction of Differential-Methylation Subtractive Library

    Directory of Open Access Journals (Sweden)

    Wei Hu

    2014-01-01

    Full Text Available Stress-induced ROS changes DNA methylation patterns. A protocol combining methylation-sensitive restriction endonuclease (MS-RE digestion with suppression subtractive hybridization (SSH to construct the differential-methylation subtractive library was developed for finding genes regulated by methylation mechanism under cold stress. The total efficiency of target fragment detection was 74.64%. DNA methylation analysis demonstrated the methylation status of target fragments changed after low temperature or DNA methyltransferase inhibitor treatment. Transcription level analysis indicated that demethylation of DNA promotes gene expression level. The results proved that our protocol was reliable and efficient to obtain gene fragments in differential-methylation status.

  8. Thraustochytrid protists degrade hydrocarbons

    Digital Repository Service at National Institute of Oceanography (India)

    Raikar, M.T.; Raghukumar, S.; Vani, V.; David, J.J.; Chandramohan, D.

    Although thraustochytrid protists are known to be of widespread occurrence in the sea, their hydrocarbon-degrading abilities have never been investigated. We isolated thraustochytrids from coastal waters and sediments of Goa coast by enriching MPN...

  9. How do polymers degrade?

    Science.gov (United States)

    Lyu, Suping

    2011-03-01

    Materials derived from agricultural products such as cellulose, starch, polylactide, etc. are more sustainable and environmentally benign than those derived from petroleum. However, applications of these polymers are limited by their processing properties, chemical and thermal stabilities. For example, polyethylene terephthalate fabrics last for many years under normal use conditions, but polylactide fabrics cannot due to chemical degradation. There are two primary mechanisms through which these polymers degrade: via hydrolysis and via oxidation. Both of these two mechanisms are related to combined factors such as monomer chemistry, chain configuration, chain mobility, crystallinity, and permeation to water and oxygen, and product geometry. In this talk, we will discuss how these materials degrade and how the degradation depends on these factors under application conditions. Both experimental studies and mathematical modeling will be presented.

  10. Degradation of implant materials

    CERN Document Server

    Eliaz, Noam

    2012-01-01

    This book surveys the degradation of implant materials, reviewing in detail such failure mechanisms as corrosion, fatigue and wear, along with monitoring techniques. Surveys common implant biomaterials, as well as procedures for implant retrieval and analysis.

  11. Environmental degradation in biocomposites

    CSIR Research Space (South Africa)

    John, Maya J

    2017-06-01

    Full Text Available molecular chain scission, surface oxidation, and breakdown of molecules to form active radicals. The main degradation processes occurring by weathering includes photoradiation, thermal degradation, photooxidation, and hydrolysis [22,23]. The effect... which exhibits transitions from glassy stage to a rubbery stage at its glass transition temperature. ● Weathering Composites commonly used in automotive and aerospace applications are subjected to varying conditions of sunlight, rain, moisture...

  12. Bacteria and lignin degradation

    Institute of Scientific and Technical Information of China (English)

    Jing LI; Hongli YUAN; Jinshui YANG

    2009-01-01

    Lignin is both the most abundant aromatic (phenolic) polymer and the second most abundant raw material.It is degraded and modified by bacteria in the natural world,and bacteria seem to play a leading role in decomposing lignin in aquatic ecosystems.Lignin-degrading bacteria approach the polymer by mechanisms such as tunneling,erosion,and cavitation.With the advantages of immense environmental adaptability and biochemical versatility,bacteria deserve to be studied for their ligninolytic potential.

  13. Whole genome methylation profiling by immunoprecipitation of methylated DNA.

    Science.gov (United States)

    Sharp, Andrew J

    2012-01-01

    I provide a protocol for DNA methylation profiling based on immunoprecipitation of methylated DNA using commercially available monoclonal antibodies that specifically recognize 5-methylcytosine. Quantification of the level of enrichment of the resulting DNA enables DNA methylation to be assayed for any genomic locus, including entire chromosomes or genomes if appropriate microarray or high-throughput sequencing platforms are used. In previous studies (1, 2), I have used hybridization to oligonucleotide arrays from Roche Nimblegen Inc, which allow any genomic region of interest to be interrogated, dependent on the array design. For example, using modern tiling arrays comprising millions of oligonucleotide probes, several complete human chromosomes can be assayed at densities of one probe per 100 bp or greater, sufficient to yield high-quality data. However, other methods such as quantitative real-time PCR or high-throughput sequencing can be used, giving either measurement of methylation at a single locus or across the entire genome, respectively. While the data produced by single locus assays is relatively simple to analyze and interpret, global assays such as microarrays or high-throughput sequencing require more complex statistical approaches in order to effectively identify regions of differential methylation, and a brief outline of some approaches is given.

  14. Polyanhydride degradation and erosion.

    Science.gov (United States)

    Göpferich, A; Tessmar, J

    2002-10-16

    It was the intention of this paper to give a survey on the degradation and erosion of polyanhydrides. Due to the multitude of polymers that have been synthesized in this class of material in recent years, it was not possible to discuss all polyanhydrides that have gained in significance based on their application. It was rather the intention to provide a broad picture on polyanhydride degradation and erosion based on the knowledge that we have from those polymers that have been intensively investigated. To reach this goal this review contains several sections. First, the foundation for an understanding of the nomenclature are laid by defining degradation and erosion which was deemed necessary because many different definitions exist in the current literature. Next, the properties of major classes of anhydrides are reviewed and the impact of geometry on degradation and erosion is discussed. A complicated issue is the control of drug release from degradable polymers. Therefore, the aspect of erosion-controlled release and drug stability inside polyanhydrides are discussed. Towards the end of the paper models are briefly reviewed that describe the erosion of polyanhydrides. Empirical models as well as Monte-Carlo-based approaches are described. Finally it is outlined how theoretical models can help to answer the question why polyanhydrides are surface eroding. A look at the microstructure and the results from these models lead to the conclusion that polyanhydrides are surface eroding due to their fast degradation. However they switch to bulk erosion once the device dimensions drop below a critical limit.

  15. Controlled methyl-esterification of pectin catalyzed by cation exchange resin.

    Science.gov (United States)

    Peng, Xiaoxia; Yang, Guang; Fan, Xingchen; Bai, Yeming; Ren, Xiaomeng; Zhou, Yifa

    2016-02-10

    This study developed a new method to methyl-esterify pectin using a cation exchange resin. Homogalacturonan (HG)-type pectin (WGPA-3-HG) and rhamnogalacturonan (RG)-I-type pectin (AHP-RG) obtained from the roots of Panax ginseng and sunflower heads, respectively, were used as models. Compared to commonly used methyl-esterification methods that use either methyl iodide or acidified methanol, the developed method can methyl-esterify both HG- and RG-I-type pectins without degrading their structures via β-elimination or acid hydrolysis. In addition, by modifying reaction conditions, including the mass ratio of resin to pectin, reaction time, and temperature, the degree of esterification can be controlled. Moreover, the resin and methanol can be recycled to conserve resources, lower costs, and reduce environmental pollution. This new methodology will be highly useful for industrial esterification of pectin.

  16. Intermittent trickling bed filter for the removal of methyl ethyl ketone and methyl isobutyl ketone.

    Science.gov (United States)

    Farnazo, Danvir Mark C; Nisola, Grace M; Han, Mideok; Yoo, Namjong; Chung, Wook-Jin

    2012-05-01

    Biodegradations of methyl ethyl ketone and methyl isobutyl ketone were performed in intermittent biotrickling filter beds (ITBF) operated at two different trickling periods: 12 h/day (ITBF-12) and 30 min/day (ITBF-0.5). Ralstonia sp. MG1 was able to degrade both ketones as evidenced by growth kinetic experiments. Results show that trickling period is an important parameter to achieve high removal performance and to maintain the robustness of Ralstonia sp. MG1. Overall, ITBF-12 outperformed ITBF-0.5 regardless of the target compound. ITBF-12 had high performance recovery at various inlet gas concentrations. The higher carbon dioxide production rates in ITBF-12 suggest higher microbial activity than in ITBF-0.5. Additionally, lower concentrations of absorbed volatile organic compound (VOC) in trickling solutions of ITBF-12 systems also indicate VOC removal through biodegradation. Pressure drop levels in ITBF-12 were relatively higher than in ITBF-0.5 systems, which can be attributed to the decrease in packed bed porosity as Ralstonia sp. MG1 grew well in ITBF-12. Nonetheless, the obtained pressure drop levels did not have any adverse effect on the performance of ITBF-12. Biokinetic constants were also obtained which indicated that ITBF-12 performed better than ITBF-0.5 and other conventional biotrickling filter systems.

  17. DDE remediation and degradation.

    Science.gov (United States)

    Thomas, John E; Ou, Li-Tse; All-Agely, Abid

    2008-01-01

    DDT and its metabolites, DDD and DDE, have been shown to be recalcitrant to degradation. The parent compound, DDT, was used extensively worldwide starting in 1939 and was banned in the United States in 1973. The daughter compound, DDE, may result from aerobic degradation, abiotic dehydrochlorination, or photochemical decomposition. DDE has also occurred as a contaminant in commercial-grade DDT. The p,p'-DDE isomer is more biologically active than the o,p-DDE, with a reported half-life of -5.7 years. However, when DDT was repeatedly applied to the soil, the DDE concentration may remain unchanged for more than 20 yr. Remediation of DDE-contaminated soil and water may be done by several techniques. Phytoremediation involves translocating DDT, DDD, and DDE from the soil into the plant, although some aquatic species (duckweed > elodea > parrot feather) can transform DDT into predominantly DDD with some DDE being formed. Of all the plants that can uptake DDE, Cucurbita pepo has been the most extensively studied, with translocation values approaching "hyperaccumulation" levels. Soil moisture, temperature, and plant density have all been documented as important factors in the uptake of DDE by Cucurbita pepo. Uptake may also be influenced positively by amendments such as biosurfactants, mycorrhizal inoculants, and low molecular weight organic acids (e.g., citric and oxalic acids). DDE microbial degradation by dehalogenases, dioxygenases, and hydrolases occurs under the proper conditions. Although several aerobic degradation pathways have been proposed, none has been fully verified. Very few aerobic pure cultures are capable of fully degrading DDE to CO2. Cometabolism of DDE by Pseudomonas sp., Alicaligens sp., and Terrabacter sp. grown on biphenyl has been reported; however, not all bacterial species that produce biphenyl dioxygenase degraded DDE. Arsenic and copper inhibit DDE degradation by aerobic microorganisms. Similarly, metal chelates such as EDTA inhibit the

  18. In vitro evaluation of N-methyl amide tripeptidomimetics as substrates for the human intestinal di-/tri-peptide transporter hPEPT1

    DEFF Research Database (Denmark)

    Andersen, Rikke; Nielsen, Carsten Uhd; Begtrup, Mikael;

    2006-01-01

    application of N-methyl amide bioisosteres as peptide bond replacements in tripeptides in order to decrease degradation by peptidases and yet retain affinity for and transport via hPEPT1. Seven structurally diverse N-methyl amide tripeptidomimetics were selected based on a principal component analysis...... of structural properties of 6859 N-methyl amide tripeptidomimetics. In vitro extracellular degradation of the selected tripeptidomimetics as well as affinity for and transepithelial transport via hPEPT1 were investigated in Caco-2 cells. Decreased apparent degradation was observed for all tripeptidomimetics...... to be substrates for hPEPT1 than tripeptidomimetics with charged side chains. The results of the present study indicate that the N-methyl amide peptide bond replacement approach for increasing bioavailability of tripeptidomimetic drug candidates is not generally applicable to all tripeptides. Nevertheless...

  19. Drift Degradation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    D. Kicker

    2004-09-16

    Degradation of underground openings as a function of time is a natural and expected occurrence for any subsurface excavation. Over time, changes occur to both the stress condition and the strength of the rock mass due to several interacting factors. Once the factors contributing to degradation are characterized, the effects of drift degradation can typically be mitigated through appropriate design and maintenance of the ground support system. However, for the emplacement drifts of the geologic repository at Yucca Mountain, it is necessary to characterize drift degradation over a 10,000-year period, which is well beyond the functional period of the ground support system. This document provides an analysis of the amount of drift degradation anticipated in repository emplacement drifts for discrete events and time increments extending throughout the 10,000-year regulatory period for postclosure performance. This revision of the drift degradation analysis was developed to support the license application and fulfill specific agreement items between the U.S. Nuclear Regulatory Commission (NRC) and the U.S. Department of Energy (DOE). The earlier versions of ''Drift Degradation Analysis'' (BSC 2001 [DIRS 156304]) relied primarily on the DRKBA numerical code, which provides for a probabilistic key-block assessment based on realistic fracture patterns determined from field mapping in the Exploratory Studies Facility (ESF) at Yucca Mountain. A key block is defined as a critical block in the surrounding rock mass of an excavation, which is removable and oriented in an unsafe manner such that it is likely to move into an opening unless support is provided. However, the use of the DRKBA code to determine potential rockfall data at the repository horizon during the postclosure period has several limitations: (1) The DRKBA code cannot explicitly apply dynamic loads due to seismic ground motion. (2) The DRKBA code cannot explicitly apply loads due to thermal

  20. Microbial degradation of herbicides.

    Science.gov (United States)

    Singh, Baljinder; Singh, Kashmir

    2016-01-01

    Herbicides remain the most effective, efficient and economical way to control weeds; and its market continues to grow even with the plethora of generic products. With the development of herbicide-tolerant crops, use of herbicides is increasing around the world that has resulted in severe contamination of the environment. The strategies are now being developed to clean these substances in an economical and eco-friendly manner. In this review, an attempt has been made to pool all the available literature on the biodegradation of key herbicides, clodinafop propargyl, 2,4-dichlorophenoxyacetic acid, atrazine, metolachlor, diuron, glyphosate, imazapyr, pendimethalin and paraquat under the following objectives: (1) to highlight the general characteristic and mode of action, (2) to enlist toxicity in animals, (3) to pool microorganisms capable of degrading herbicides, (4) to discuss the assessment of herbicides degradation by efficient microbes, (5) to highlight biodegradation pathways, (6) to discuss the molecular basis of degradation, (7) to enlist the products of herbicides under degradation process, (8) to highlight the factors effecting biodegradation of herbicides and (9) to discuss the future aspects of herbicides degradation. This review may be useful in developing safer and economic microbiological methods for cleanup of soil and water contaminated with such compounds.

  1. Effect of salinity on mercury methylating benthic microbes and their activities in Great Salt Lake, Utah.

    Science.gov (United States)

    Boyd, Eric S; Yu, Ri-Qing; Barkay, Tamar; Hamilton, Trinity L; Baxter, Bonnie K; Naftz, David L; Marvin-DiPasquale, Mark

    2017-03-01

    Surface water and biota from Great Salt Lake (GSL) contain some of the highest documented concentrations of total mercury (THg) and methylmercury (MeHg) in the United States. In order to identify potential biological sources of MeHg and controls on its production in this ecosystem, THg and MeHg concentrations, rates of Hg(II)-methylation and MeHg degradation, and abundances and compositions of archaeal and bacterial 16 rRNA gene transcripts were determined in sediment along a salinity gradient in GSL. Rates of Hg(II)-methylation were inversely correlated with salinity and were at or below the limits of detection in sediment sampled from areas with hypersaline surface water. The highest rates of Hg(II)-methylation were measured in sediment with low porewater salinity, suggesting that benthic microbial communities inhabiting less saline environments are supplying the majority of MeHg in the GSL ecosystem. The abundance of 16S rRNA gene transcripts affiliated with the sulfate reducer Desulfobacterium sp. was positively correlated with MeHg concentrations and Hg(II)-methylation rates in sediment, indicating a potential role for this taxon in Hg(II)-methylation in low salinity areas of GSL. Reactive inorganic Hg(II) (a proxy used for Hg(II) available for methylation) and MeHg concentrations were inversely correlated with salinity. Thus, constraints imposed by salinity on Hg(II)-methylating populations and the availability of Hg(II) for methylation are inferred to result in higher MeHg production potentials in lower salinity environments. Benthic microbial MeHg degradation was also most active in lower salinity environments. Collectively, these results suggest an important role for sediment anoxia and microbial sulfate reducers in the production of MeHg in low salinity GSL sub-habitats and may indicate a role for salinity in constraining Hg(II)-methylation and MeHg degradation activities by influencing the availability of Hg(II) for methylation.

  2. Effect of salinity on mercury methylating benthic microbes and their activities in Great Salt Lake, Utah

    Science.gov (United States)

    Boyd, Eric S.; Yu, Ri-Qing; Barkay, Tamar; Hamilton, Trinity L.; Baxter, Bonnie K.; Naftz, David L.; Marvin-DiPasquale, Mark

    2017-01-01

    Surface water and biota from Great Salt Lake (GSL) contain some of the highest documented concentrations of total mercury (THg) and methylmercury (MeHg) in the United States. In order to identify potential biological sources of MeHg and controls on its production in this ecosystem, THg and MeHg concentrations, rates of Hg(II)-methylation and MeHg degradation, and abundances and compositions of archaeal and bacterial 16 rRNA gene transcripts were determined in sediment along a salinity gradient in GSL. Rates of Hg(II)-methylation were inversely correlated with salinity and were at or below the limits of detection in sediment sampled from areas with hypersaline surface water. The highest rates of Hg(II)-methylation were measured in sediment with low porewater salinity, suggesting that benthic microbial communities inhabiting less saline environments are supplying the majority of MeHg in the GSL ecosystem. The abundance of 16S rRNA gene transcripts affiliated with the sulfate reducer Desulfobacterium sp. was positively correlated with MeHg concentrations and Hg(II)-methylation rates in sediment, indicating a potential role for this taxon in Hg(II)-methylation in low salinity areas of GSL. Reactive inorganic Hg(II) (a proxy used for Hg(II) available for methylation) and MeHg concentrations were inversely correlated with salinity. Thus, constraints imposed by salinity on Hg(II)-methylating populations and the availability of Hg(II) for methylation are inferred to result in higher MeHg production potentials in lower salinity environments. Benthic microbial MeHg degradation was also most active in lower salinity environments. Collectively, these results suggest an important role for sediment anoxia and microbial sulfate reducers in the production of MeHg in low salinity GSL sub-habitats and may indicate a role for salinity in constraining Hg(II)-methylation and MeHg degradation activities by influencing the availability of Hg(II) for methylation.

  3. Histone Methylation by Temozolomide; A Classic DNA Methylating Anticancer Drug

    Science.gov (United States)

    Pickard, Amanda J.; Diaz, Anthony Joseph; Mura, Hugo; Nyuwen, Lila; Coello, Daniel; Sheva, Saif; Maria, Nava; Gallo, James M.; Wang, Tieli

    2017-01-01

    Background/Aim The alkylating agent, temozolomide (TMZ), is considered the standard-of-care for high-grade astrocytomas –known as glioblastoma multiforme (GBM)– an aggressive type of tumor with poor prognosis. The therapeutic benefit of TMZ is attributed to formation of DNA adducts involving the methylation of purine bases in DNA. We investigated the effects of TMZ on arginine and lysine amino acids, histone H3 peptides and histone H3 proteins. Materials and Methods Chemical modification of amino acids, histone H3 peptide and protein by TMZ was performed in phosphate buffer at physiological pH. The reaction products were examined by mass spectrometry and western blot analysis. Results Our results showed that TMZ following conversion to a methylating cation, can methylate histone H3 peptide and histone H3 protein, suggesting that TMZ exerts its anticancer activity not only through its interaction with DNA, but also through alterations of protein post-translational modifications. Conclusion The possibility that TMZ can methylate histones involved with epigenetic regulation of protein indicates a potentially unique mechanism of action. The study will contribute to the understanding the anticancer activity of TMZ in order to develop novel targeted molecular strategies to advance the cancer treatment. PMID:27354585

  4. Motor degradation prediction methods

    Energy Technology Data Exchange (ETDEWEB)

    Arnold, J.R.; Kelly, J.F.; Delzingaro, M.J.

    1996-12-01

    Motor Operated Valve (MOV) squirrel cage AC motor rotors are susceptible to degradation under certain conditions. Premature failure can result due to high humidity/temperature environments, high running load conditions, extended periods at locked rotor conditions (i.e. > 15 seconds) or exceeding the motor`s duty cycle by frequent starts or multiple valve stroking. Exposure to high heat and moisture due to packing leaks, pressure seal ring leakage or other causes can significantly accelerate the degradation. ComEd and Liberty Technologies have worked together to provide and validate a non-intrusive method using motor power diagnostics to evaluate MOV rotor condition and predict failure. These techniques have provided a quick, low radiation dose method to evaluate inaccessible motors, identify degradation and allow scheduled replacement of motors prior to catastrophic failures.

  5. Development of a sensor for polypropylene degradation products.

    Energy Technology Data Exchange (ETDEWEB)

    Sawyer, Patricia Sue; Howell, Stephen Wayne; Hochrein, James Michael; Dirk, Shawn M.; Bernstein, Robert; Washburn, Cody M.; Graf, Darin C.

    2009-04-01

    This paper presents the development of a sensor to detect the oxidative and radiation induced degradation of polypropylene. Recently we have examined the use of crosslinked assemblies of nanoparticles as a chemiresistor-type sensor for the degradation products. We have developed a simple method that uses a siloxane matrix to fabricate a chemiresistor-type sensor that minimizes the swelling transduction mechanism while optimizing the change in dielectric response. These sensors were exposed with the use of a gas chromatography system to three previously identified polypropylene degradation products including 4-methyl-2-pentanone, acetone, and 2-pentanone. The limits of detection 210 ppb for 4-methy-2-pentanone, 575 ppb for 2-pentanone, and the LoD was unable to be determined for acetone due to incomplete separation from the carbon disulfide carrier.

  6. Degradation of organic pollutants by Ag, Cu and Sn doped waste non-metallic printed circuit boards.

    Science.gov (United States)

    Ramaswamy, Kadari; Radha, Velchuri; Malathi, M; Vithal, Muga; Munirathnam, Nagegownivari R

    2017-02-01

    The disposal and reuse of waste printed circuit boards have been the major global concerns. Printed circuit boards, a form of Electronic waste (hereafter e-waste), have been chemically processed, doped with Ag(+), Cu(2+) and Sn(2+), and used as visible light photocatalysts against the degradation of methylene blue and methyl violet. The elemental analyses of pristine and metal doped printed circuit board were obtained using energy dispersive X-ray fluorescence (EDXRF) spectra and inductively coupled plasma optical emission spectroscopy (ICP-OES). The morphology of parent and doped printed circuit board was obtained from scanning electron microscopy (SEM) measurements. The photocatalytic activity of parent and metal doped samples was carried out for the decomposition of organic pollutants, methylene blue and methyl violet, under visible light irradiation. Metal doped waste printed circuit boards (WPCBs) have shown higher photocatalytic activity against the degradation of methyl violet and methylene blue under visible light irradiation. Scavenger experiments were performed to identify the reactive intermediates responsible for the degradation of methylene blue and methyl violet. The reactive species responsible for the degradation of MV and MB were found to be holes and hydroxyl radicals. A possible mechanism of degradation of methylene blue and methyl violet is given. The stability and reusability of the catalysts are also investigated.

  7. Antifoam degradation testing

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, D. P. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River Ecology Lab. (SREL); Zamecnik, J. R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River Ecology Lab. (SREL); Newell, D. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River Ecology Lab. (SREL); Williams, M. S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River Ecology Lab. (SREL)

    2015-08-20

    This report describes the results of testing to quantify the degradation products resulting from the dilution and storage of Antifoam 747. Antifoam degradation is of concern to the Defense Waste Processing Facility (DWPF) due to flammable decomposition products in the vapor phase of the Chemical Process Cell vessels, as well as the collection of flammable and organic species in the offgas condensate. The discovery that hexamethyldisiloxane is formed from the antifoam decomposition was the basis for a Potential Inadequacy in the Safety Analysis declaration by the DWPF.

  8. Photovoltaic Degradation Risk: Preprint

    Energy Technology Data Exchange (ETDEWEB)

    Jordan, D. C.; Kurtz, S. R.

    2012-04-01

    The ability to accurately predict power delivery over the course of time is of vital importance to the growth of the photovoltaic (PV) industry. Important cost drivers include the efficiency with which sunlight is converted into power, how this relationship changes over time, and the uncertainty in this prediction. An accurate quantification of power decline over time, also known as degradation rate, is essential to all stakeholders - utility companies, integrators, investors, and researchers alike. In this paper we use a statistical approach based on historical data to quantify degradation rates, discern trends and quantify risks related to measurement uncertainties, number of measurements and methodologies.

  9. HYDROCARBON-DEGRADING BACTERIA AND SURFACTANT ACTIVITY

    Energy Technology Data Exchange (ETDEWEB)

    Brigmon, R; Topher Berry, T; Grazyna A. Plaza, G; jacek Wypych, j

    2006-08-15

    Fate of benzene ethylbenzene toluene xylenes (BTEX) compounds through biodegradation was investigated using two different bacteria, Ralstonia picketti (BP-20) and Alcaligenes piechaudii (CZOR L-1B). These bacteria were isolated from extremely polluted petroleum hydrocarbon contaminated soils. PCR and Fatty Acid Methyl Ester (FAME) were used to identify the isolates. Biodegradation was measured using each organism individually and in combination. Both bacteria were shown to degrade each of the BTEX compounds. Alcaligenes piechaudii biodegraded BTEXs more efficiently while mixed with BP-20 and individually. Biosurfactant production was observed by culture techniques. In addition 3-hydroxy fatty acids, important in biosurfactant production, was observed by FAME analysis. In the all experiments toluene and m+p- xylenes were better growth substrates for both bacteria than the other BTEX compounds. In addition, the test results indicate that the bacteria could contribute to bioremediation of aromatic hydrocarbons (BTEX) pollution increase biodegradation through the action by biosurfactants.

  10. Degradation of parabens by Pseudomonas beteli and Burkholderia latens.

    Science.gov (United States)

    Amin, Aeshna; Chauhan, Sateesh; Dare, Manish; Bansal, Arvind Kumar

    2010-06-01

    p-Hydroxybenzoic acid esters (parabens) are commonly used antimicrobial preservatives in pharmaceutical formulations. Two microorganisms, isolated from non-sterile methyl paraben (MP) and propyl paraben (PP) solutions, were found to degrade the respective parabens. Identification by 16S rRNA partial gene sequencing revealed them to be Pseudomonas beteli and Burkholderia latens, respectively. The present work describes a previously unreported interaction of the parabens with P. beteli and B. latens. Degradation of MP at various concentrations by P. beteli, followed a logarithmic pattern, while that of PP by B. latens was found to be linear. It was subsequently observed that P. beteli could degrade only MP, while B. latens could degrade both the parabens. Absence of HPLC chromatogram peaks of expected degradation products indicated that the parabens were used up as a carbon source. The behaviour of pathogens (Pseudomonas aeruginosa, Staphylococcus aureus, Candida albicans and Aspergillus niger) of the pharmacopoeial preservative effectiveness test (PET), towards MP, showed that none had the ability to degrade the paraben. It was concluded that, for a paraben-preserved multi-dose ophthalmic formulation, the sole use of the four pathogens that are recommended by the pharmacopoeia for PET can falsely indicate the formulation to be effective against 'in-use' contamination.

  11. The preparation of nano-composite Ag-H6P2W18062/Ti02 and microwave assisted photocatalytic degradation of methyl orange%纳米复合材料Ag-H6P2W18O62/TiO2的制备与微波辅助光催化甲基橙

    Institute of Scientific and Technical Information of China (English)

    蒋新德; 邢北平; 计远; 张文治; 李莉

    2012-01-01

    The nano-composite material Ag-H6P2W18O62/TiO2 in this study was prepared by sol-gel method combined with temperature-programmed hydrothermal treatment. The phase structures, chemical composition, opticalabsorption properties and surface physicochemical properties were characterized via FTIR, ICP-AES, XRD, nitrogen adsorption/desorption and TEM. The results showed the basic structure of polyoxometaltes in the composites has been basicly matained. The composites Ag-H6P2W18O62/TiO2 are periodical mesoporous materials, and the silver species existing in the nano-composite Ag-H6P2W18O62/TiO2 was metallic Ag. The photocatalytic activities of the as-prepared material were studied by the microwave assisted photodegradation of methyl orange. The results showed that the photocatalytic activitiy of Ag-H6P2W18O62/TiO2 for methyl orange was higher.%采用溶胶一凝胶再结合程序升温溶剂热一步法制备了纳米复合光催化材料Ag-HeP2WtsOJTiO2,并采用傅立叶一红外光谱(FT-IR)、等离子原子反射光谱(ICP-AES)、氮气吸附一脱附测定和透射电子显微镜(TEM)等测试方法Ag-H6P2W18O62/TiO2合成材料的物理化学性质进行了表征。结果表明,复合材料中母体多酸的基本结构未发生明显变化,其Agl)J单质形式存在,且显示为介孔材料。在微波场作用下,复合材料Ag-H6P2W18O62/TiO2对甲基橙的降解表现了较高的催化活性。

  12. APPLICATION OF PHOTOCATALYTIC PROCESS FOR REMOVAL OF METHYL TERT-BUTYL ETHER FROM HIGHLYCONTAMINATED WATER

    Directory of Open Access Journals (Sweden)

    A. Mesdaghinia

    2007-09-01

    Full Text Available The oxygenate methyl tert-butyl ether is added to gasoline to increase the octane level and to reduce carbon monoxide and hydrocarbon emissions by vehicles. The high mobility, water solubility, and resistance to natural attenuation associated with methyl tert-butyl ether may result in contamination of ground and surface waters. In this research the degradation of aqueous methyl tert-butyl ether at relatively high concentrations was investigated by UV-vis/TiO2/H2O2 photocatalytic process. The effect of important operational parameters such as pH, amount of H2O2, catalyst loading, and irradiation time were also studied. Concentrations of methyl tert-butyl ether and intermediates such as tert-butyl formate and tert-butyl alcohol were measured over a 180 min period using a gas chromatograph equipped with flame ionization detector and combined with headspace sampler. Results showed that the time required for complete degradation increased from 30 to 180min, when the initial concentration was increased from 10 to 500mg/L. The first order rate constant for degradation of methyl tert-butyl ether from the hydroxyl radical was estimated to be 0.177 to 0.022 1/min as the concentration increased from 10 to 500mg/L. Study on the overall mineralization monitored by total organic carbon (TOC analysis showed that in the initial concentration of 100mg/L methyl tert-butyl ether, complete mineralization was obtained after 110min under UV-vis/TiO2/H2O2 photocatalytic process.

  13. Methyl 3-(4-methylbenzylidenecarbazate

    Directory of Open Access Journals (Sweden)

    Yu-Feng Li

    2010-06-01

    Full Text Available The title compound, C10H12N2O2, was prepared by the reaction of methyl carbazate and 4-methylbenzaldehyde. The dihedral angle between the benzene ring and the carbazate fragment is 20.86 (10°. In the crystal structure, molecules are linked by intermolecular N—H...O hydrogen bonds.

  14. Bacterial production of methyl ketones

    Energy Technology Data Exchange (ETDEWEB)

    Beller, Harry R.; Goh, Ee-Been

    2017-01-31

    The present invention relates to methods and compositions for increasing production of methyl ketones in a genetically modified host cell that overproduces .beta.-ketoacyl-CoAs through a re-engineered .beta.-oxidation pathway and overexpresses FadM.

  15. Water Column Methylation in Estuaries

    Science.gov (United States)

    Schartup, A. T.; Calder, R.; Soerensen, A. L.; Mason, R. P.; Balcom, P. H.; Sunderland, E. M.

    2014-12-01

    Methylmercury (MeHg) is a neurotoxin that bioaccumulates in aquatic food webs and affects humans and wildlife through fish consumption. Many studies have measured active methylation/demethylation in ocean margin sediments but few have reported similar rates for the marine water column. This presentation will review available evidence for water column methylation in estuaries, including new experimental measurements of methylation/demethylation rates from a deep subarctic fjord in Labrador Canada collected in Spring and Fall of 2012-2013. We used these and other data to construct a mass budget for MeHg in the estuary and show that water column methylation (with rates ranging from 1.5 to 2.8 % day-1), is the largest contributor, followed by inputs from rivers (4.9 mol year-1), to the in situ pool of MeHg available for uptake by biota. By contrast, the sediment in this system is a net sink for MeHg (-1.5 mol year-1). We discuss the relationship between observed MeHg and other ancillary environmental factors (organic carbon, sulfur and nutrients) as well as implications for the response time of fish to future changes in mercury inputs.

  16. Identification of body fluid-specific DNA methylation markers for use in forensic science.

    Science.gov (United States)

    Park, Jong-Lyul; Kwon, Oh-Hyung; Kim, Jong Hwan; Yoo, Hyang-Sook; Lee, Han-Chul; Woo, Kwang-Man; Kim, Seon-Young; Lee, Seung-Hwan; Kim, Yong Sung

    2014-11-01

    DNA methylation, which occurs at the 5'-position of the cytosine in CpG dinucleotides, has great potential for forensic identification of body fluids, because tissue-specific patterns of DNA methylation have been demonstrated, and DNA is less prone to degradation than proteins or RNA. Previous studies have reported several body fluid-specific DNA methylation markers, but DNA methylation differences are sometimes low in saliva and vaginal secretions. Moreover, specific DNA methylation markers in four types of body fluids (blood, saliva, semen, and vaginal secretions) have not been investigated with genome-wide profiling. Here, we investigated novel DNA methylation markers for identification of body fluids for use in forensic science using the Illumina HumanMethylation 450K bead array, which contains over 450,000 CpG sites. Using methylome data from 16 samples of blood, saliva, semen, and vaginal secretions, we first selected 2986 hypermethylated or hypomethylated regions that were specific for each type of body fluid. We then selected eight CpG sites as novel, forensically relevant DNA methylation markers: cg06379435 and cg08792630 for blood, cg26107890 and cg20691722 for saliva, cg23521140 and cg17610929 for semen, and cg01774894 and cg14991487 for vaginal secretions. These eight selected markers were evaluated in 80 body fluid samples using pyrosequencing, and all showed high sensitivity and specificity for identification of the target body fluid. We suggest that these eight DNA methylation markers may be good candidates for developing an effective molecular assay for identification of body fluids in forensic science.

  17. Biodegradation of the gasoline oxygenates methyl tert-butyl ether, ethyl tert-butyl ether, and tert-amyl methyl ether by propane-oxidizing bacteria.

    Science.gov (United States)

    Steffan, R J; McClay, K; Vainberg, S; Condee, C W; Zhang, D

    1997-11-01

    Several propane-oxidizing bacteria were tested for their ability to degrade gasoline oxygenates, including methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME). Both a laboratory strain and natural isolates were able to degrade each compound after growth on propane. When propane-grown strain ENV425 was incubated with 20 mg of uniformly labeled [14C]MTBE per liter, the strain converted > 60% of the added MTBE to 14CO2 in production of nearly stoichiometric amounts of tert-butyl alcohol (TBA), while the initial oxidation of TAME resulted in the production of tert-amyl alcohol. The methoxy methyl group of MTBE was oxidized to formaldehyde and ultimately to CO2. TBA was further oxidized to 2-methyl-2-hydroxy-1-propanol and then 2-hydroxy isobutyric acid; however, neither of these degradation products was an effective growth substrate for the propane oxidizers. Analysis of cell extracts of ENV425 and experiments with enzyme inhibitors implicated a soluble P-450 enzyme in the oxidation of both MTBE and TBA. MTBE was oxidized to TBA by camphor-grown Pseudomonas putida CAM, which produces the well-characterized P-450cam, but not by Rhodococcus rhodochrous 116, which produces two P-450 enzymes. Rates of MTBE degradation by propane-oxidizing strains ranged from 3.9 to 9.2 nmol/min/mg of cell protein at 28 degrees C, whereas TBA was oxidized at a rate of only 1.8 to 2.4 nmol/min/mg of cell protein at the same temperature.

  18. Bacterial Degradation of Pesticides

    DEFF Research Database (Denmark)

    Knudsen, Berith Elkær

    could potentially improve bioremediation of BAM. An important prerequisite for bioaugmentation is the potential to produce the degrader strain at large quantities within reasonable time. The aim of manuscript II, was to optimize the growth medium for Aminobacter MSH1 and to elucidate optimal growth...

  19. Research on N, Ni TiO2 light of the preparation of catalysts doped and the methyl violet degradation performance%N、Ni共掺杂TiO2光催化剂的制备及对亚甲基紫降解性能研究

    Institute of Scientific and Technical Information of China (English)

    马威; 高航; 张艳惠; 李松田

    2012-01-01

    以硫脲、硝酸镍、钛酸四丁酯为原料,用溶胶-凝胶法制备了纯TiO2和不同比例N、Ni掺杂的TiO2的光催化剂样品,用紫外-可见分光光度计进行了表征.结果表明,经过掺杂的TiO2光催化剂的吸收边向可见光方向移动,TiO2可见光催化活性提高,掺杂量为0.15g,pH =9,温度为30 ℃时,对亚甲基紫的脱色效果最好.%With thiourea, nitric acid nickel, tetra butyl titanate ester as raw material and using sol-gel process with different proportion of pure TiO2 and N, Ni TiO2 light catalysts doped samples. By UV-Vis spectra photometry instrument was characterized. Results showed that after doped the absorption of TiO2 light catalyst to visible direction, edge of TiO2 visible catalytic activity improved, doping quantity 0.15 g, pH =9 and for 30 ℃ the methyl violet decoloration rate the best effect.

  20. Multivariate optimization for electrochemical oxidation of methyl orange: Pathway identification and toxicity analysis.

    Science.gov (United States)

    Pillai, Indu M Sasidharan; Gupta, Ashok K; Tiwari, Manoj K

    2015-01-01

    Electrochemical oxidation of methyl orange (Sodium 4-[(4-dimethylamino) phenyldiazenyl] benzenesulfonate) with lead dioxide coated on mild steel was modelled using response surface methodology (RSM) to analyze the influence of pH, NaCl dose and current on color and chemical oxygen demand (COD) removal. Higher current, acidic pH and 0.8-1.2 g L(-1) NaCl dose had an enhancing effect on the removal efficiencies. Interaction effect of the variables highlights the action of (•)OH and HOCl in the oxidation of methyl orange, where HOCl has effect at lower current range. More than 90% COD removal efficiency and ∼100% color removal efficiency was obtained in 5 h at optimum conditions for an initial concentration of 50 mg L(-1). High performance liquid chromatography-mass spectroscopy (HPLC-MS) analysis carried out to identify degradation intermediates revealed the absence of chlorinated intermediates, which was further verified with Fourier transform infrared spectroscopy (FTIR) analysis. The postulated pathway of degradation indicated breakdown through dealkylation, deamination, desulfonation and cleavage of an azo bond and benzene ring. The degradation of methyl orange to smaller compounds was also confirmed by Ion Chromatography (IC). Cytotoxicity analysis on HaCaT cells revealed the intermediates to be more cytotoxic than the dye, possibly due to the aromatic amines and diazines formed during the degradation process.

  1. STUDY OF METHYL ORANGE PHOTODEGRADATION USING TiO2-MONTMORILLONITE COMPOSITE

    OpenAIRE

    2015-01-01

    Composite TiO2-montmorillonite (Ti-MMT) has been synthesized with the aim to improve the ability of TiO2 photocatalysts degrade methyl orange. Synthesis of composite made by mixing TiO2 and montmorillonite in ethanol solution, then heated using the furnace at a temperature of 450 °C for 5 hours. TiO2-MMT composites were characterized by FT-IR, XRD and SAA. Test photodegradation activity of TiO2-MMT composites made to dye Methyl Orange 8 mg / L with UV light irradiation time variation and mass...

  2. Electronic transport in methylated fragments of DNA

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, M. L. de; Oliveira, J. I. N.; Lima Neto, J. X.; Gomes, C. E. M.; Fulco, U. L., E-mail: umbertofulco@gmail.com; Albuquerque, E. L. [Departamento de Biofísica e Farmacologia, Universidade Federal do Rio Grande do Norte, 59072-970 Natal-RN (Brazil); Freire, V. N. [Departamento de Física, Universidade Federal do Ceará, 60455-760 Fortaleza, CE (Brazil); Caetano, E. W. S. [Instituto Federal de Educação, Ciência e Tecnologia do Ceará, 60040-531 Fortaleza, CE (Brazil); Moura, F. A. B. F. de; Lyra, M. L. [Instituto de Física, Universidade Federal de Alagoas, 57072-900 Maceió-AL (Brazil)

    2015-11-16

    We investigate the electronic transport properties of methylated deoxyribonucleic-acid (DNA) strands, a biological system in which methyl groups are added to DNA (a major epigenetic modification in gene expression), sandwiched between two metallic platinum electrodes. Our theoretical simulations apply an effective Hamiltonian based on a tight-binding model to obtain current-voltage curves related to the non-methylated/methylated DNA strands. The results suggest potential applications in the development of novel biosensors for molecular diagnostics.

  3. Adenine N6-methylation in diverse fungi.

    Science.gov (United States)

    Seidl, Michael F

    2017-05-26

    A DNA modification-methylation of cytosines and adenines-has important roles in diverse processes such as regulation of gene expression and genome stability, yet until recently adenine methylation had been considered to be only a hallmark of prokaryotes. A new study identifies abundant adenine methylation of transcriptionally active genes in early-diverging fungi that, together with recent other work, emphasizes the importance of adenine methylation in eukaryotes.

  4. DNA Methylation Signatures of the Plant Chromomethyltransferases

    OpenAIRE

    Gouil, Quentin; Baulcombe, David C

    2016-01-01

    DNA methylation in plants is traditionally partitioned into CG, CHG and CHH contexts (with H any nucleotide but G). By investigating DNA methylation patterns in trinucleotide contexts in four angiosperm species, we show that such a representation hides spatial and functional partitioning of different methylation pathways and is incomplete. CG methylation (mCG) is largely context-independent whereas, at CHG motifs, there is under-representation of mCCG in pericentric regions of A. thaliana and...

  5. Detection of pump degradation

    Energy Technology Data Exchange (ETDEWEB)

    Greene, R.H.; Casada, D.A.; Ayers, C.W. [and others

    1995-08-01

    This Phase II Nuclear Plant Aging Research study examines the methods of detecting pump degradation that are currently employed in domestic and overseas nuclear facilities. This report evaluates the criteria mandated by required pump testing at U.S. nuclear power plants and compares them to those features characteristic of state-of-the-art diagnostic programs and practices currently implemented by other major industries. Since the working condition of the pump driver is crucial to pump operability, a brief review of new applications of motor diagnostics is provided that highlights recent developments in this technology. The routine collection and analysis of spectral data is superior to all other technologies in its ability to accurately detect numerous types and causes of pump degradation. Existing ASME Code testing criteria do not require the evaluation of pump vibration spectra but instead overall vibration amplitude. The mechanical information discernible from vibration amplitude analysis is limited, and several cases of pump failure were not detected in their early stages by vibration monitoring. Since spectral analysis can provide a wealth of pertinent information concerning the mechanical condition of rotating machinery, its incorporation into ASME testing criteria could merit a relaxation in the monthly-to-quarterly testing schedules that seek to verify and assure pump operability. Pump drivers are not included in the current battery of testing. Operational problems thought to be caused by pump degradation were found to be the result of motor degradation. Recent advances in nonintrusive monitoring techniques have made motor diagnostics a viable technology for assessing motor operability. Motor current/power analysis can detect rotor bar degradation and ascertain ranges of hydraulically unstable operation for a particular pump and motor set. The concept of using motor current or power fluctuations as an indicator of pump hydraulic load stability is presented.

  6. Methylation of Gibberellins by Arabidopsis GAMT1 and GAMT2

    Energy Technology Data Exchange (ETDEWEB)

    Varbanova,M.; Yamaguchi, S.; Yang, Y.; McKelvey, K.; Hanada, A.; Borochov, R.; Yu, F.; Jikumaru, Y.; Ross, J.; et al

    2007-01-01

    Arabidopsis thaliana GAMT1 and GAMT2 encode enzymes that catalyze formation of the methyl esters of gibberellins (GAs). Ectopic expression of GAMT1 or GAMT2 in Arabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency and typical GA deficiency phenotypes, such as dwarfism and reduced fertility. GAMT1 and GAMT2 are both expressed mainly in whole siliques (including seeds), with peak transcript levels from the middle until the end of silique development. Within whole siliques, GAMT2 was previously shown to be expressed mostly in developing seeds, and we show here that GAMT1 expression is also localized mostly to seed, suggesting a role in seed development. Siliques of null single GAMT1 and GAMT2 mutants accumulated high levels of various GAs, with particularly high levels of GA1 in the double mutant. Methylated GAs were not detected in wild-type siliques, suggesting that methylation of GAs by GAMT1 and GAMT2 serves to deactivate GAs and initiate their degradation as the seeds mature. Seeds of homozygous GAMT1 and GAMT2 null mutants showed reduced inhibition of germination, compared with the wild type, when placed on plates containing the GA biosynthesis inhibitor ancymidol, with the double mutant showing the least inhibition. These results suggest that the mature mutant seeds contained higher levels of active GAs than wild-type seeds.

  7. NOVEL EMBEDDED CERAMIC ELECTRODE SYSTEM TO ACTIVATE NANOSTRUCTURED TITANIUM DIOXIDE FOR DEGRADATION OF MTBE

    Science.gov (United States)

    A novel reactor combining a flame-deposited nanostructured titanium dioxide film and a set of embedded ceramic electrodes was designed, developed and tested for degradation of methyl tert-butyl ether (MTBE) in water. On applying a voltage to the ceramic electrodes, a surface coro...

  8. Degradation of the herbicide mecoprop in an aerobic aquifer determined by laboratory batch studies

    DEFF Research Database (Denmark)

    Heron, Gorm; Christensen, Thomas Højlund

    1992-01-01

    The potential of a shallow aerobic aquifer to degrade the herbicide Mecoprop (2-(2-methyl-4-chlorophenoxy)propionic acid) was evaluated in the laboratory using groundwater and sediment suspension batches. Mecoprop was added to the batches to obtain concentrations of 65, 140, 400 and 1400 μg/l. Me...

  9. Microwave-assisted Fenton-like decolorization of methyl orange solution using chromium compounds

    Institute of Scientific and Technical Information of China (English)

    LIU Zuo-hua; TAO Chang-yuan; DU Jun; SUN Da-gui; LI Bai-zhan

    2008-01-01

    Azo dyes discharged in the environment are persistent organic pollutants (POPs), which are very difficult to remove. We developed a microwave-assisted Fenton-like process to degrade methyl orange (MO), an azo dye, with hydrogen peroxide (H2O2) catalyzed by chromium compounds coexisting with MO in the solution. Comparison between the Cr(III)-H2O2 and Cr(VI)-H2O2 systems shows that Cr(VI) has a stronger and more stable catalytical activity than Cr(III), and Cr(III) is more susceptible to a change in the acidity or alkalinity of the reaction system. With a Cr(VI) concentration of 10 mmol L-1 or a Cr(III) concentration of 12 mmol L-1 in the solution under the microwave irradiation of a power larger than 300 W for 3 min, 10 mmol L-1 H2O2 can degrade more than 95% of 1 000 mg L-1 methyl orange; when the microwave power is increased to 700 W, the same amount of H2O2 can degrade all methyl orange in the solution with the same amount of Cr(VI) catalyst. Ultraviolet-visible spectrography indicates the cleavage of the azo bond in methyl orange after treatment, suggesting the potential of this Fenton-like process to degrade azo dye POPs. Reusing waste chromium compounds coexisting with dyestuff in wastewater to catalyze the degradation of azo dyes could be a cost-effective technique for azo dyes and chromate manufacturers and/or users to treat their wastewater and prevent POPs from endangering the environment. This is of particular importance to controlling the water quality of the Three Gorges Reservoir.

  10. The role of methylation in urological tumours

    NARCIS (Netherlands)

    Heijden, A.G. van der

    2013-01-01

    Alterations in DNA methylation have been described in human cancer for more than thirty years now. Since the last decade DNA methylation gets more and more important in cancer research. In this review the different alterations of DNA methylation are discussed in testicular germ cell tumours, Wilms't

  11. Quantitative DNA Methylation Profiling in Cancer.

    Science.gov (United States)

    Ammerpohl, Ole; Haake, Andrea; Kolarova, Julia; Siebert, Reiner

    2016-01-01

    Epigenetic mechanisms including DNA methylation are fundamental for the regulation of gene expression. Epigenetic alterations can lead to the development and the evolution of malignant tumors as well as the emergence of phenotypically different cancer cells or metastasis from one single tumor cell. Here we describe bisulfite pyrosequencing, a technology to perform quantitative DNA methylation analyses, to detect aberrant DNA methylation in malignant tumors.

  12. Reduced methylation of PFKFB3 in cancer cells shunts glucose towards the pentose phosphate pathway.

    Science.gov (United States)

    Yamamoto, Takehiro; Takano, Naoharu; Ishiwata, Kyoko; Ohmura, Mitsuyo; Nagahata, Yoshiko; Matsuura, Tomomi; Kamata, Aki; Sakamoto, Kyoko; Nakanishi, Tsuyoshi; Kubo, Akiko; Hishiki, Takako; Suematsu, Makoto

    2014-03-17

    Haem oxygenase (HO)-1/carbon monoxide (CO) protects cancer cells from oxidative stress, but the gas-responsive signalling mechanisms remain unknown. Here we show using metabolomics that CO-sensitive methylation of PFKFB3, an enzyme producing fructose 2,6-bisphosphate (F-2,6-BP), serves as a switch to activate phosphofructokinase-1, a rate-limiting glycolytic enzyme. In human leukaemia U937 cells, PFKFB3 is asymmetrically di-methylated at R131 and R134 through modification by protein arginine methyltransferase 1. HO-1 induction or CO results in reduced methylation of PFKFB3 in varied cancer cells to suppress F-2,6-BP, shifting glucose utilization from glycolysis toward the pentose phosphate pathway. Loss of PFKFB3 methylation depends on the inhibitory effects of CO on haem-containing cystathionine β-synthase (CBS). CBS modulates remethylation metabolism, and increases NADPH to supply reduced glutathione, protecting cells from oxidative stress and anti-cancer reagents. Once the methylation of PFKFB3 is reduced, the protein undergoes polyubiquitination and is degraded in the proteasome. These results suggest that the CO/CBS-dependent regulation of PFKFB3 methylation determines directional glucose utilization to ensure resistance against oxidative stress for cancer cell survival.

  13. Degradation of environmental pollutants by Trametes trogii.

    Science.gov (United States)

    Haglund, C; Levín, L; Forchiassin, F; López, M; Viale, A

    2002-01-01

    The ability of the ligninolytic fungus Trametes trogii to degrade in vitro different xenobiotics (PCBs, PAHs and dyes) was evaluated. Either 200 ppm of a PCB mixture (Aroclor 1150) or 160 ppm of an industrial PAH mixture (10% V/V of PAHs, principal components hexaethylbenzene, naphthalene, 1-methyl naphthalene, acenaphthylene, anthracene, fluorene and phenanthrene), were added to trophophasic and idiophasic cultures growing in a nitrogen limited mineral medium (glucose/asparagine) and in a complex medium (malt extract/glucose). Gas-liquid chromatography proved that within 7 to 12 d more than 90% of the organopollutants added were removed. The decrease in absorbance at 620 nm demonstrated that cultures of this fungus were able to transform 80% of the dye Anthraquinone-blue (added at a concentration of 50 ppm) in 1.5 h. Enzyme estimations indicated high activity of laccase (up to 0.55 U/mL), as well as lower production of manganese-peroxidase. Laccase activity, detected in all the conditions assayed, could be implicated in the degradation of these organopollutants. Considering the results obtained, T. trogii seems promising for detoxification.

  14. Endocytic collagen degradation

    DEFF Research Database (Denmark)

    Madsen, Daniel H.; Jürgensen, Henrik J.; Ingvarsen, Signe;

    2012-01-01

    it crucially important to understand both the collagen synthesis and turnover mechanisms in this condition. Here we show that the endocytic collagen receptor, uPARAP/Endo180, is a major determinant in governing the balance between collagen deposition and degradation. Cirrhotic human livers displayed a marked......Fibrosis of the liver and its end-stage, cirrhosis, represent major health problems worldwide. In these fibrotic conditions, activated fibroblasts and hepatic stellate cells display a net deposition of collagen. This collagen deposition is a major factor leading to liver dysfunction, thus making...... up-regulation of uPARAP/Endo180 in activated fibroblasts and hepatic stellate cells located close to the collagen deposits. In a hepatic stellate cell line, uPARAP/Endo180 was shown to be active in, and required for, the uptake and intracellular degradation of collagen. To evaluate the functional...

  15. Nylon separators. [thermal degradation

    Science.gov (United States)

    Lim, H. S.

    1977-01-01

    A nylon separator was placed in a flooded condition in K0H solution and heated at various high temperatures ranging from 60 C to 110 C. The weight decrease was measured and the molecular weight and decomposition product were analyzed to determine: (1) the effect of K0H concentration on the hydrolysis rate; (2) the effect of K0H concentration on nylon degradation; (3) the activation energy at different K0H concentrations; and (4) the effect of oxygen on nylon degradation. The nylon hydrolysis rate is shown to increase as K0H concentration is decreased 34%, giving a maximum rate at about 16%. Separator hydrolysis is confirmed by molecular weight decrease in age of the batteries, and the reaction of nylon with molecular oxygen is probably negligible, compared to hydrolysis. The extrapolated rate value from the high temperature experiment correlates well with experimental values at 35 degrees.

  16. TALSPEAK Solvent Degradation

    Energy Technology Data Exchange (ETDEWEB)

    Leigh R. Martin; Bruce J. Mincher

    2009-09-01

    Understanding the radiolytic degradation behavior of organic molecules involved in new or existing schemes for the recycle of used nuclear fuels is of significant interest for sustaining a closed nuclear fuel cycle. Here we have conducted several lines of investigation to begin understanding the effects of radiolysis on the aqueous phase of the TALSPEAK process for the separation of the trivalent lanthanides from the trivalent actinides. Using the 60-Co irradiator at the INL, we have begun to quantify the effects of radiation on the aqueous phase complexants used in this separation technique, and how this will affect the actinide lanthanide separation factor. In addition we have started to develop methodologies for stable product identification, a key element in determining the degradation pathways. We have also introduced a methodology to investigate the effects of alpha radiolysis that has previously received limited attention.

  17. miRNAting control of DNA methylation

    Indian Academy of Sciences (India)

    Ashwani Jha; Ravi Shankar

    2014-06-01

    DNA methylation is a type of epigenetic modification where a methyl group is added to the cytosine or adenine residue of a given DNA sequence. It has been observed that DNA methylation is achieved by some collaborative agglomeration of certain proteins and non-coding RNAs. The assembly of IDN2 and its homologous proteins with siRNAs recruits the enzyme DRM2, which adds a methyl group at certain cytosine residues within the DNA sequence. In this study, it was found that de novo DNA methylation might be regulated by miRNAs through systematic targeting of the genes involved in DNA methylation. A comprehensive genome-wide and system-level study of miRNA targeting, transcription factors, DNA-methylation-causing genes and their target genes has provided a clear picture of an interconnected relationship of all these factors which regulate DNA methylation in Arabidopsis. The study has identified a DNA methylation system that is controlled by four different genes: IDN2, IDNl1, IDNl2 and DRM2. These four genes along with various critical transcription factors appear to be controlled by five different miRNAs. Altogether, DNA methylation appears to be a finely tuned process of opposite control systems of DNA-methylation-causing genes and certain miRNAs pitted against each other.

  18. Detection of pump degradation

    Energy Technology Data Exchange (ETDEWEB)

    Casada, D. [Oak Ridge National Lab., TN (United States)

    1995-04-01

    There are a variety of stressors that can affect the operation of centrifugal pumps. Although these general stressors are active in essentially all centrifugal pumps, the stressor level and the extent of wear and degradation can vary greatly. Parameters that affect the extent of stressor activity are manifold. In order to assure the long-term operational readiness of a pump, it is important to both understand the nature and magnitude of the specific degradation mechanisms and to monitor the performance of the pump. The most commonly applied method of monitoring the condition of not only pumps, but rotating machinery in general, is vibration analysis. Periodic or continuous special vibration analysis is a cornerstone of most pump monitoring programs. In the nuclear industry, non-spectral vibration monitoring of safety-related pumps is performed in accordance with the ASME code. Pump head and flow rate are also monitored, per code requirements. Although vibration analysis has dominated the condition monitoring field for many years, there are other measures that have been historically used to help understand pump condition; advances in historically applied technologies and developing technologies offer improved monitoring capabilities. The capabilities of several technologies (including vibration analysis, dynamic pressure analysis, and motor power analysis) to detect the presence and magnitude of both stressors and resultant degradation are discussed.

  19. Methods in DNA methylation profiling.

    Science.gov (United States)

    Zuo, Tao; Tycko, Benjamin; Liu, Ta-Ming; Lin, Juey-Jen L; Huang, Tim H-M

    2009-12-01

    Metastable and somatically heritable patterns of DNA methylation provide an important level of genomic regulation. In this article, we review methods for analyzing these genome-wide epigenetic patterns and offer a perspective on the ever-expanding literature, which we hope will be useful for investigators who are new to this area. The historical aspects that we cover will be helpful in interpreting this literature and we hope that our discussion of the newest analytical methods will stimulate future progress. We emphasize that no single approach can provide a complete view of the overall methylome, and that combinations of several modalities applied to the same sample set will give the clearest picture. Given the unexpected epigenomic patterns and new biological principles, as well as new disease markers, that have been uncovered in recent studies, it is likely that important discoveries will continue to be made using genome-wide DNA methylation profiling.

  20. DNA methylation in hepatocellular carcinoma

    Institute of Scientific and Technical Information of China (English)

    Iris Tischoff; Andrea Tannapfel

    2008-01-01

    As for many other tumors, development of hepatocellular carcinoma (HCC) must be understood as a multistep process with accumulation of genetic and epigenetic alterations in regulatory genes, leading to activation of oncogenes and inactivation or loss of tumor suppressor genes (TSG). In the last decades, in addition to genetic alterations, epigenetic inactivation of (tumor suppressor) genes by promoter hypermethylation has been recognized as an important and alternative mechanism in tumorigenesis. In HCC, aberrant methylation of promoter sequences occurs not only in advanced tumors, it has been also observed in premalignant conditions just as chronic viral hepatitis B or C and cirrhotic liver. This review discusses the epigenetic alterations in hepatocellular carcinoma focusing DNA methylation.

  1. Methylated genes as new cancer biomarkers.

    LENUS (Irish Health Repository)

    Duffy, M J

    2012-02-01

    Aberrant hypermethylation of promoter regions in specific genes is a key event in the formation and progression of cancer. In at least some situations, these aberrant alterations occur early in the formation of malignancy and appear to be tumour specific. Multiple reports have suggested that measurement of the methylation status of the promoter regions of specific genes can aid early detection of cancer, determine prognosis and predict therapy responses. Promising DNA methylation biomarkers include the use of methylated GSTP1 for aiding the early diagnosis of prostate cancer, methylated PITX2 for predicting outcome in lymph node-negative breast cancer patients and methylated MGMT in predicting benefit from alkylating agents in patients with glioblastomas. However, prior to clinical utilisation, these findings require validation in prospective clinical studies. Furthermore, assays for measuring gene methylation need to be standardised, simplified and evaluated in external quality assurance programmes. It is concluded that methylated genes have the potential to provide a new generation of cancer biomarkers.

  2. DNA methylation profiling of hematopoietic stem cells.

    Science.gov (United States)

    Begtrup, Amber Hogart

    2014-01-01

    DNA methylation is a key epigenetic mark that is essential for properly functioning hematopoietic stem cells. Determining where functionally relevant DNA methylation marks exist in the genome is crucial to understanding the role that methylation plays in hematopoiesis. This chapter describes a method to profile DNA methylation by selectively enriching methylated DNA sequences that are bound in vitro by methyl-binding domain (MBD) proteins. The MBD-pulldown approach selects for DNA sequences that have the potential to be "read" by the endogenous machinery involved in epigenetic regulation. Furthermore, this approach is feasible with very small quantities of DNA, and is compatible with the use of any downstream high-throughput sequencing approach. This technique offers a reliable, simple, and powerful tool for exploration of the role of DNA methylation in hematopoietic stem cells.

  3. Conventional and nanotechniques for DNA methylation profiling.

    Science.gov (United States)

    Shanmuganathan, Rajasree; Basheer, Nazeema B; Amirthalingam, Laxmi; Muthukumar, Harshiny; Kaliaperumal, Rajendran; Shanmugam, Kumaran

    2013-01-01

    DNA methylation is critical for gene silencing and is associated with the incidence of many diseases, including cancer. Underlying molecular mechanisms of human diseases and tissue-specific gene expression have been elucidated based on DNA methylation studies. This review highlights the advantages and drawbacks of various methylation screening techniques: blotting, genomic sequencing, bisulfite sequencing, methylation-specific PCR, methylated DNA immunoprecipitation, microarray analysis, matrix-assisted laser desorption ionization time-of-flight mass spectroscopy, nanowire transistor detection procedure, quantum dot-based nanoassay, single-molecule real-time detection, fluorimetric assay, electrochemical detection, and atomic force spectroscopy. The review provides insight for selecting a method or a combination of methods for DNA methylation analysis. Convergence of conventional and contemporary nanotechniques to enumerate methylation at specific CpG sites of oncogene would fill the gap in diagnosis of cancer.

  4. Biogeochemical Cycles in Degraded Lands

    Science.gov (United States)

    Davidson, Eric A.; Vieira, Ima Celia G.; ReisdeCarvalho, Claudio Jose; DeanedeAbreuSa, Tatiana; deSouzaMoutinho, Paulo R.; Figueiredo, Ricardo O.; Stone, Thomas A.

    2004-01-01

    The objectives of this project were to define and describe the types of landscapes that fall under the broad category of "degraded lands" and to study biogeochemical cycles across this range of degradation found in secondary forests. We define degraded land as that which has lost part of its capacity of renovation of a productive ecosystem, either in the context of agroecosystems or as native communities of vegetation. This definition of degradation permits evaluation of biogeochemical constraints to future land uses.

  5. Putting muscle in DNA methylation

    Institute of Scientific and Technical Information of China (English)

    James P Reddington; Richard R Meehan

    2011-01-01

    Over 25 years ago seminal experiments from the labs of Peter Jones and Harold Weintraub demonstrated that alteration in the DNA modification state underlie the myogenic conversion of fibroblast cell lines [1,2].This paved the way for the identification of myogenic helix-loop-helix (HLH) proteins in muscle differentiation,but the mechanism by which DNA methylation regulates muscle differentiation has remained elusive [3].

  6. Metal oxide semiconductors for dye degradation

    Energy Technology Data Exchange (ETDEWEB)

    Adhikari, Sangeeta; Sarkar, Debasish, E-mail: dsarkar@nitrkl.ac.in

    2015-12-15

    Highlights: • Hydrothermal synthesis of monoclinic and hexagonal WO{sub 3} nanostructures. • Nanocuboid and nanofiber growth using different structure directing agents. • WO{sub 3}–ZnO nanocomposites for dye degradation under UV and visible light. • High photocatalytic efficiency is achieved by 10 wt% monoclinic WO{sub 3}. • WO{sub 3} assists to trap hole in UV and arrests electron in visible light irradiation. - Abstract: Organic contaminants are a growing threat to the environment that widely demands their degradation by high efficient photocatalysts. Thus, the proposed research work primely focuses on the efficient degradation of methyl orange using designed WO{sub 3}–ZnO photocatalysts under both UV and visible light irradiation. Two different sets of WO{sub 3} nanostructures namely, monoclinic WO{sub 3} (m-WO{sub 3}) and hexagonal WO{sub 3} (h-WO{sub 3}) synthesizes in presence of a different structure directing agents. A specific dispersion technique allows the intimate contact of as-synthesized WO{sub 3} and ultra-violet active commercial ZnO photocatalyst in different weight variations. ZnO nanocrystal in presence of an optimum 10 wt% m-WO{sub 3} shows a high degree of photocatalytic activity under both UV and visible light irradiation compared to counterpart h-WO{sub 3}. Symmetrical monoclinic WO{sub 3} assists to trap hole in UV, but electron arresting mechanism predominates in visible irradiation. Coupling of monoclinic nanocuboid WO{sub 3} with ZnO proves to be a promising photocatalyst in both wavelengths.

  7. Ordered bulk degradation via autophagy

    DEFF Research Database (Denmark)

    Dengjel, Jörn; Kristensen, Anders Riis; Andersen, Jens S

    2008-01-01

    at proteasomal and lysosomal degradation ample cross-talk between the two degradation pathways became evident. Degradation via autophagy appeared to be ordered and regulated at the protein complex/organelle level. This raises several important questions such as: can macroautophagy itself be specific and what...

  8. Environmental occurrence and degradation of the herbicide n-chloridazon.

    Science.gov (United States)

    Buttiglieri, Gianluigi; Peschka, Manuela; Frömel, Tobias; Müller, Jutta; Malpei, Francesca; Seel, Peter; Knepper, Thomas P

    2009-06-01

    A sampling campaign was carried out for n-chloridazon (n-CLZ) and its degradation product desphenyl-chloridazon (DPC) in the Hesse region (Germany) during the year 2007: a total of 548 environmental samples including groundwater, surface water and wastewater treatment plant (WWTP) effluent were analysed. Furthermore, aerobic degradation of n-CLZ has been studied utilising a fixed bed bioreactor (FBBR). In surface water, n-CLZ was detected at low concentrations (average 0.01+/-0.06mugL(-1); maximum 0.89mugL(-1)) with a seasonal peak, whereas DPC was present throughout the year at much higher concentrations (average 0.72+/-0.81mugL(-1); maximum 7.4mugL(-1)). Higher n-CLZ concentrations were observed in the North compared with South Hesse, which is ascribed to a higher density of agricultural areas. Furthermore, methylated DPC (Me-DPC), another degradation product, was detected in surface water. In the degradation test, n-CLZ was completely converted to DPC at all concentrations tested (Me-DPC was not formed under the test conditions). DPC was resistant to further degradation during the whole experimental period of 98 days. The results obtained suggest persistence and high dispersion of DPC in the aquatic environment.

  9. Enhanced regeneration of degraded polymer solar cells by thermal annealing

    Science.gov (United States)

    Kumar, Pankaj; Bilen, Chhinder; Feron, Krishna; Zhou, Xiaojing; Belcher, Warwick J.; Dastoor, Paul C.

    2014-05-01

    The degradation and thermal regeneration of poly(3-hexylethiophene) (P3HT):[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) and P3HT:indene-C60 bisadduct (ICBA) polymer solar cells, with Ca/Al and Ca/Ag cathodes and indium tin oxide/poly(ethylene-dioxythiophene):polystyrene sulfonate anode have been investigated. Degradation occurs via a combination of three primary pathways: (1) cathodic oxidation, (2) active layer phase segregation, and (3) anodic diffusion. Fully degraded devices were subjected to thermal annealing under inert atmosphere. Degraded solar cells possessing Ca/Ag electrodes were observed to regenerate their performance, whereas solar cells having Ca/Al electrodes exhibited no significant regeneration of device characteristics after thermal annealing. Moreover, the solar cells with a P3HT:ICBA active layer exhibited enhanced regeneration compared to P3HT:PCBM active layer devices as a result of reduced changes to the active layer morphology. Devices combining a Ca/Ag cathode and P3HT:ICBA active layer demonstrated ˜50% performance restoration over several degradation/regeneration cycles.

  10. Degradation of herbicides in shallow Danish aquifers - an integrated laboratory and field study

    DEFF Research Database (Denmark)

    Albrechtsen, Hans-Jørgen; Mills, M.; Aamand, J.

    2001-01-01

    , results were compared. Some herbicides were degraded under aerobic conditions (some phenoxy acids, DNOC and glyphosate) and others under aerobic conditions (other phenoxy acids, DNOC; there was some indication of atrazine transformation). Certain pesticides were not degraded in any investigations......Degradation of pesticides in aquifers has been evaluated based on a number of co-ordinated field and laboratory studies carried out in Danish aquifers. These studies included investigations of vertical and horizontal variability in degradation rates from the vadose zone to an aquifer, the effects...... (dichlobenil, the dichlobenil metabolite 2,6-dichlorobenzamide (BAM), bentazone, isoproturon, metarnitron and metsulfuron-methyl). The spatial variability was substantial, since hardly any of the investigated pesticides were degraded in all comparable samples. This means that it is very difficult to claim...

  11. First evidence of DNA methylation in insect Tribolium castaneum: environmental regulation of DNA methylation within heterochromatin.

    Science.gov (United States)

    Feliciello, Isidoro; Parazajder, Josip; Akrap, Ivana; Ugarković, Durđica

    2013-05-01

    DNA methylation has been studied in many eukaryotic organisms, in particular vertebrates, and was implicated in developmental and phenotypic variations. Little is known about the role of DNA methylation in invertebrates, although insects are considered as excellent models for studying the evolution of DNA methylation. In the red flour beetle, Tribolium castaneum (Tenebrionidae, Coleoptera), no evidence of DNA methylation has been found till now. In this paper, a cytosine methylation in Tribolium castaneum embryos was detected by methylation sensitive restriction endonucleases and immuno-dot blot assay. DNA methylation in embryos is followed by a global demethylation in larvae, pupae and adults. DNA demethylation seems to proceed actively through 5-hydroxymethylcytosine, most probably by the action of TET enzyme. Bisulfite sequencing of a highly abundant satellite DNA located in pericentromeric heterochromatin revealed similar profile of cytosine methylation in adults and embryos. Cytosine methylation was not only restricted to CpG sites but was found at CpA, CpT and CpC sites. In addition, complete cytosine demethylation of heterochromatic satellite DNA was induced by heat stress. The results reveal existence of DNA methylation cycling in T. castaneum ranging from strong overall cytosine methylation in embryos to a weak DNA methylation in other developmental stages. Nevertheless, DNA methylation is preserved within heterochromatin during development, indicating its role in heterochromatin formation and maintenance. It is, however, strongly affected by heat stress, suggesting a role for DNA methylation in heterochromatin structure modulation during heat stress response.

  12. Statistical modeling for degradation data

    CERN Document Server

    Lio, Yuhlong; Ng, Hon; Tsai, Tzong-Ru

    2017-01-01

    This book focuses on the statistical aspects of the analysis of degradation data. In recent years, degradation data analysis has come to play an increasingly important role in different disciplines such as reliability, public health sciences, and finance. For example, information on products’ reliability can be obtained by analyzing degradation data. In addition, statistical modeling and inference techniques have been developed on the basis of different degradation measures. The book brings together experts engaged in statistical modeling and inference, presenting and discussing important recent advances in degradation data analysis and related applications. The topics covered are timely and have considerable potential to impact both statistics and reliability engineering.

  13. Bacterial degradation of detergent compounds.

    Science.gov (United States)

    Goodnow, R A; Harrison, A P

    1972-10-01

    A survey for surfactant degradation among aerobic bacteria has been undertaken. Tests have been made in peptone medium where such a degradation, if it occurs, will be gratuitous. Tallow-alkyl-sulfate, alkyl-ethoxylate-sulfate, and linear-alkyl-benzene-sulfonate were used. Forty-five strains of 34 species in 19 genera degrade one or more of these detergent compounds. With some species, the surfactant inhibits degradation without inhibiting growth, whereas with one species slight degradation took place even at a toxic concentration of surfactant.

  14. The Atmospheric Chemistry of Methyl Chavicol (Estragole)

    Science.gov (United States)

    Bloss, W. J.; Alam, M. S.; Rickard, A. R.; Hamilton, J. F.; Pereira, K. F.; Camredon, M.; Munoz, A.; Vazquez, M.; Alacreu, P.; Rodenas, M.; Vera, T.

    2012-12-01

    The oxidation of volatile organic compounds (VOCs) leads to formation of ozone and secondary organic aerosols (SOA), with consequences for health, air quality, crop yields, atmospheric chemistry and radiative transfer. It is estimated that ca. 90 % of VOC emissions to the atmosphere originate from biogenic sources (BVOC); such emissions may increase under future climates. Recent field observations have identified Methyl Chavicol ("MC" hereafter, also known as Estragole; 1-allyl-4-methoxybenzene, C10H12O) as a major BVOC above pine forests in the USA [Bouvier-Brown et al., 2009], and within an oil palm plantation in Malaysian Borneo, where it was found that MC could represent the highest single floral contribution of reactive carbon to the atmosphere [Misztal et al., 2010]. Palm oil cultivation, and hence emissions of MC, may be expected to increase with societal food and biofuel demand. We present the results of a series of simulation chamber experiments to assess the atmospheric fate of MC. Experiments were performed in the EUPHORE (European Photoreactor) facility in Valencia, Spain (200 m3 outdoor smog chamber), investigating the degradation of MC by reaction with OH, O3 and NO3. An extensive range of measurement instrumentation was used to monitor precursor and product formation, including stable species (FTIR, PTR-MS, GC-FID and GC-MS), radical intermediates (LIF), inorganic components (NOx, O3, HONO (LOPAP and aerosol production (SMPS) and composition (PILS and filters; analysed offline by LC-MS and FTICR-MS). Experiments were conducted at a range of NOx:VOC ratios, and in the presence and absence of radical (OH) scavenger compounds. This chamber dataset is used to determine the rate constants for reaction of MC with OH, O3 and NO3, the ozonolysis radical yields, and identify the primary degradation products for each initiation route, alongside the aerosol mass yields. Aerosol composition measurements are analysed to identify markers for MC contributions to

  15. Evolution of DNA Methylation across Insects.

    Science.gov (United States)

    Bewick, Adam J; Vogel, Kevin J; Moore, Allen J; Schmitz, Robert J

    2017-03-01

    DNA methylation contributes to gene and transcriptional regulation in eukaryotes, and therefore has been hypothesized to facilitate the evolution of plastic traits such as sociality in insects. However, DNA methylation is sparsely studied in insects. Therefore, we documented patterns of DNA methylation across a wide diversity of insects. We predicted that underlying enzymatic machinery is concordant with patterns of DNA methylation. Finally, given the suggestion that DNA methylation facilitated social evolution in Hymenoptera, we tested the hypothesis that the DNA methylation system will be associated with presence/absence of sociality among other insect orders. We found DNA methylation to be widespread, detected in all orders examined except Diptera (flies). Whole genome bisulfite sequencing showed that orders differed in levels of DNA methylation. Hymenopteran (ants, bees, wasps and sawflies) had some of the lowest levels, including several potential losses. Blattodea (cockroaches and termites) show all possible patterns, including a potential loss of DNA methylation in a eusocial species whereas solitary species had the highest levels. Species with DNA methylation do not always possess the typical enzymatic machinery. We identified a gene duplication event in the maintenance DNA methyltransferase 1 (DNMT1) that is shared by some Hymenoptera, and paralogs have experienced divergent, nonneutral evolution. This diversity and nonneutral evolution of underlying machinery suggests alternative DNA methylation pathways may exist. Phylogenetically corrected comparisons revealed no evidence that supports evolutionary association between sociality and DNA methylation. Future functional studies will be required to advance our understanding of DNA methylation in insects. © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

  16. Surface properties of Yarrowia lipolytica and their relevance to γ-decalactone formation from methyl ricinoleate

    OpenAIRE

    Aguedo, Mario; Waché, Y.; Belin, J.-M.; Teixeira, J. A

    2005-01-01

    The surface of the lipid-degrading yeast, Yarrowia lipolytica, was characterized by contact angle and zeta potential (ζ) measurements. The cells were mainly hydrophilic with a negative charge that was only affected from pH 2 to 4. To study the effects of the surface charges on the biotransformation of methyl ricinoleate into the aroma compound, γ-decalactone, the ζ values of the substrate droplets were modified by adding a cationic surfactant into the medium at concentrations that...

  17. Purification and sequence analysis of 4-methyl-5-nitrocatechol oxygenase from Burkholderia sp. strain DNT.

    OpenAIRE

    Haigler, B E; Suen, W C; Spain, J C

    1996-01-01

    4-Methyl-5-nitrocatechol (MNC) is an intermediate in the degradation of 2,4-dinitrotoluene by Burkholderia sp. strain DNT. In the presence of NADPH and oxygen, MNC monooxygenase catalyzes the removal of the nitro group from MNC to form 2-hydroxy-5-methylquinone. The gene (dntB) encoding MNC monooxygenase has been previously cloned and characterized. In order to examine the properties of MNC monooxygenase and to compare it with other enzymes, we sequenced the gene encoding the MNC monooxygenas...

  18. Photodegradation of methyl orange by BiOI-sensitized TiO_2

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    BiOI-sensitized titanium dioxide (TiO2) photocatalysts were prepared by a deposition method at room temperature and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller surface area measurements. The photocatalytic activities of the catalysts were evaluated for the degradation of methyl orange (MO) solution under UV and visible light irradiation. The effects of catalyst amount, initial pH value, initial concentration of MO, as well as KI amount were investigated. ...

  19. Degradation of copepod fecal pellets

    DEFF Research Database (Denmark)

    Poulsen, Louise K.; Iversen, Morten

    2008-01-01

    Copepod fecal pellets are often degraded at high rates within the upper part of the water column. However, the identity of the degraders and the processes governing the degradation remain unresolved. To identify the pellet degraders we collected water from Oresund (Denmark) approximately every...... second month from July 2004 to July 2005. These water samples were divided into 5 fractions (pellet degradation rate and species composition of the plankton from triplicate incubations of each fraction and a known, added...... amount of fecal pellets. The total degradation rate of pellets by the natural plankton community of Oresund followed the phytoplankton biomass, with maximum degradation rate during the spring bloom (2.5 +/- 0.49 d(-1)) and minimum (0.52 +/- 0.14 d(-1)) during late winter. Total pellet removal rate ranged...

  20. Photothermal degradation studies

    Science.gov (United States)

    Liang, R. H.

    1985-01-01

    Key reaction intermediates of photooxidation identified and characterized by laser flash Electron Spin Resonance (ESR) spectroscopy were discussed. Effects of temperature and ultraviolet intensity were studied in order to develop meaningful accelerated testing procedures for encapsulant evaluation. In a program to study the failure of Tedlar/ethylene vinyl acetate (EVA)/stainless steel modules, failure modes similar to those observed outdoors in real-time conditions were simulated in accelerated testing. An experimental technique was developed to quantitatively assess the extent of degradation.

  1. Fatty Acid Structure and Degradation Analysis in Fingerprint Residues

    Science.gov (United States)

    Pleik, Stefanie; Spengler, Bernhard; Schäfer, Thomas; Urbach, Dieter; Luhn, Steven; Kirsch, Dieter

    2016-09-01

    GC-MS investigations were carried out to elucidate the aging behavior of unsaturated fatty acids in fingerprint residues and to identify their degradation products in aged samples. For this purpose, a new sample preparation technique for fingerprint residues was developed that allows producing N-methyl- N-trimethylsilyl-trifluoroacetamide (MSTFA) derivatives of the analyzed unsaturated fatty acids and their degradation products. MSTFA derivatization catalyzed by iodotrimethylsilane enables the reliable identification of aldehydes and oxoacids as characteristic MSTFA derivatives in GCMS. The obtained results elucidate the degradation pathway of unsaturated fatty acids. Our study of aged fingerprint residues reveals that decanal is the main degradation product of the observed unsaturated fatty acids. Furthermore, oxoacids with different chain lengths are detected as specific degradation products of the unsaturated fatty acids. The detection of the degradation products and their chain length is a simple and effective method to determine the double bond position in unsaturated compounds. We can show that the hexadecenoic and octadecenoic acids found in fingerprint residues are not the pervasive fatty acids Δ9-hexadecenoic (palmitoleic acid) and Δ9-octadecenoic (oleic acid) acid but Δ6-hexadecenoic acid (sapienic acid) and Δ8-octadecenoic acid. The present study focuses on the structure identification of human sebum-specific unsaturated fatty acids in fingerprint residues based on the identification of their degradation products. These results are discussed for further investigations and method developments for age determination of fingerprints, which is still a tremendous challenge because of several factors affecting the aging behavior of individual compounds in fingerprints.

  2. Biodegradation of methyl parathion and p-nitrophenol by a newly isolated Agrobacterium sp. strain Yw12.

    Science.gov (United States)

    Wang, Shenghui; Zhang, Chen; Yan, Yanchun

    2012-02-01

    Strain Yw12, isolated from activated sludge, could completely degrade and utilize methyl parathion as the sole carbon, phosphorus and energy sources for growth in the basic salt media. It could also completely degrade and utilize p-nitrophenol as the sole carbon and energy sources for growth in the minimal salt media. Phenotypic features, physiological and biochemical characteristics, and phylogenetic analysis of 16S rRNA sequence showed that this strain belongs to the genus of Agrobacterium sp. Response surface methodology was used to optimize degradation conditions. Under its optimal degradation conditions, 50 mg l(-1) MP was completely degraded within 2 h by strain Yw12 and the degradation product PNP was also completely degraded within 6 h. Furthermore, strain Yw12 could also degrade phoxim, methamidophos, chlorpyrifos, carbofuran, deltamethrin and atrazine when provided as the sole carbon and energy sources. Enzymatic analysis revealed that the MP degrading enzyme of strain Yw12 is an intracellular enzyme and is expressed constitutively. These results indicated that strain Yw12 might be used as a potential and effective organophosphate pesticides degrader for bioremediation of contaminated sites.

  3. Preparation of TiO2 Nanoparticle Loaded MCM-41 and Study of Its Photo-Catalytic Activity Towards Decolorization of Methyl Orange.

    Science.gov (United States)

    Naik, Bhanudas; Hazra, Subhenjit; Dayananda, Desagani; Prasad, V S; Ghosh, Narendra Nath

    2015-09-01

    Here we report the synthesis of TiO2 nanoparticle loaded mesoporous MCM-41 photocatalysts for degradation of methyl orange dye in aqueous medium under sunlight exposure. TiO2 loaded MCM-41 was synthesized by impregnation method. Anatase form of TiO2 nanoparticles were formed in the porous matrix of the silicate MCM-41. The synthesized materials were characterized using powder X-ray diffraction method, surface area and porosimetry analysis; diffuse reflectance analysis, particle size analysis and transmission electron microscopy. The photocatalytic property of the synthesized materials were investigated towards the degradation of methyl orange under sunlight exposure and monitored by UV-visible spectrophotometer. Synthesized catalysts showed high photocatalytic activity for the degradation of methyl orange.

  4. Enhanced decolorization of methyl orange using zero-valent copper nanoparticles under assistance of hydrodynamic cavitation.

    Science.gov (United States)

    Li, Pan; Song, Yuan; Wang, Shuai; Tao, Zheng; Yu, Shuili; Liu, Yanan

    2015-01-01

    The rate of reduction reactions of zero-valent metal nanoparticles is restricted by their agglomeration. Hydrodynamic cavitation was used to overcome the disadvantage in this study. Experiments for decolorization of methyl orange azo dye by zero-valent copper nanoparticles were carried out in aqueous solution with and without hydrodynamic cavitation. The results showed that hydrodynamic cavitation greatly accelerated the decolorization rate of methyl orange. The size of nanoparticles was decreased after hydrodynamic cavitation treatment. The effects of important operating parameters such as discharge pressure, initial solution pH, and copper nanoparticle concentration on the degradation rates were studied. It was observed that there was an optimum discharge pressure to get best decolorization performance. Lower solution pH were favorable for the decolorization. The pseudo-first-order kinetic constant for the degradation of methyl orange increased linearly with the copper dose. UV-vis spectroscopic and Fourier transform infrared (FT-IR) analyses confirmed that many degradation intermediates were formed. The results indicated hydroxyl radicals played a key role in the decolorization process. Therefore, the enhancement of decolorization by hydrodynamic cavitation could due to the deagglomeration of nanoparticles as well as the oxidation by the in situ generated hydroxyl radicals. These findings greatly increase the potential of the Cu(0)/hydrodynamic cavitation technique for use in the field of treatment of wastewater containing hazardous materials.

  5. Rat myocardial protein degradation.

    Science.gov (United States)

    Steer, J H; Hopkins, B E

    1981-07-01

    1. Myocardial protein degradation rates were determined by following tyrosine release from rat isolated left hemi-atria in vitro. 2. After two 20 min preincubations the rate of tyrosine release from hemi-atria was constant for 4 h. 3. Skeletal muscle protein degradation was determined by following tyrosine release from rat isolated hemi-diaphragm (Fulks, Li & Goldberg, 1975). 4. Insulin (10(-7) M) inhibited tyrosine release from hemi-atria and hemi-diaphragm to a similar extent. A 48 h fast increased tyrosine release rate from hemi-diaphragm and decreased tyrosine release rate from hemi-atria. Hemi-diaphragm tyrosine release was inhibited by 15 mmol/l D-glucose but a variety of concentrations of D-glucose (0, 5, 15 mmol/l) had no effect on tyrosine release from hemi-atria. Five times the normal plasma levels of the branched-chain amino acids leucine, isoleucine and valine had no effect on tyrosine release from either hemi-atria or hemi-diaphragm.

  6. Degradability of dental ceramics.

    Science.gov (United States)

    Anusavice, K J

    1992-09-01

    The degradation of dental ceramics generally occurs because of mechanical forces or chemical attack. The possible physiological side-effects of ceramics are their tendency to abrade opposing dental structures, the emission of radiation from radioactive components, the roughening of their surfaces by chemical attack with a corresponding increase in plaque retention, and the release of potentially unsafe concentrations of elements as a result of abrasion and dissolution. The chemical durability of dental ceramics is excellent. With the exception of the excessive exposure to acidulated fluoride, ammonium bifluoride, or hydrofluoric acid, there is little risk of surface degradation of virtually all current dental ceramics. Extensive exposure to acidulated fluoride is a possible problem for individuals with head and/or neck cancer who have received large doses of radiation. Such fluoride treatment is necessary to minimize tooth demineralization when saliva flow rates have been reduced because of radiation exposure to salivary glands. Porcelain surface stains are also lost occasionally when abraded by prophylaxis pastes and/or acidulated fluoride. In each case, the solutes are usually not ingested. Further research that uses standardized testing procedures is needed on the chemical durability of dental ceramics. Accelerated durability tests are desirable to minimize the time required for such measurements. The influence of chemical durability on surface roughness and the subsequent effect of roughness on wear of the ceramic restorations as well as of opposing structures should also be explored on a standardized basis.

  7. The genetic basis for bacterial mercury methylation.

    Science.gov (United States)

    Parks, Jerry M; Johs, Alexander; Podar, Mircea; Bridou, Romain; Hurt, Richard A; Smith, Steven D; Tomanicek, Stephen J; Qian, Yun; Brown, Steven D; Brandt, Craig C; Palumbo, Anthony V; Smith, Jeremy C; Wall, Judy D; Elias, Dwayne A; Liang, Liyuan

    2013-03-15

    Methylmercury is a potent neurotoxin produced in natural environments from inorganic mercury by anaerobic bacteria. However, until now the genes and proteins involved have remained unidentified. Here, we report a two-gene cluster, hgcA and hgcB, required for mercury methylation by Desulfovibrio desulfuricans ND132 and Geobacter sulfurreducens PCA. In either bacterium, deletion of hgcA, hgcB, or both genes abolishes mercury methylation. The genes encode a putative corrinoid protein, HgcA, and a 2[4Fe-4S] ferredoxin, HgcB, consistent with roles as a methyl carrier and an electron donor required for corrinoid cofactor reduction, respectively. Among bacteria and archaea with sequenced genomes, gene orthologs are present in confirmed methylators but absent in nonmethylators, suggesting a common mercury methylation pathway in all methylating bacteria and archaea sequenced to date.

  8. An Integrated Workflow for DNA Methylation Analysis

    Institute of Scientific and Technical Information of China (English)

    Pingchuan Li; Feray Demirci; Gayathri Mahalingam; Caghan Demirci; Mayumi Nakano; Blake C.Meyers

    2013-01-01

    The analysis of cytosine methylation provides a new way to assess and describe epigenetic regulation at a whole-genome level in many eukaryotes.DNA methylation has a demonstrated role in the genome stability and protection,regulation of gene expression and many other aspects of genome function and maintenance.BS-seq is a relatively unbiased method for profiling the DNA methylation,with a resolution capable of measuring methylation at individual cytosines.Here we describe,as an example,a workflow to handle DNA methylation analysis,from BS-seq library preparation to the data visualization.We describe some applications for the analysis and interpretation of these data.Our laboratory provides public access to plant DNA methylation data via visualization tools available at our "Next-Gen Sequence" websites (http://mpss.udel.edu),along with small RNA,RNA-seq and other data types.

  9. Detection of DNA methylation in eucaryotic cells.

    Directory of Open Access Journals (Sweden)

    Lech Chyczewski

    2008-01-01

    Full Text Available The methods of molecular biology allow for analyzing the methylation pattern in the whole genome and in particular genes. We differentiate methylated sequences from unmethylated ones by means of cutting the genomic template with methylation-sensitive restriction enzymes or by sodium bisulfite DNA modification. Chemical modification precedes most quantitative and qualitative PCR techniques: MS-PCR, MS-nested PCR, Real-Time PCR, QAMA, HeavyMethyl, MSHRM. Restriction enzymes, on the other hand, may be used together with PCR or hybridisation methods (Southern blot and microarrays. PCRs are conducted with primers specific for methylated and unmethylated sequences and sometimes, similarly to hybridisation techniques, with specifically labeled probes or dyes intercalating to double-stranded nucleic acids. The most advanced methylation detection techniques (MALDI-TOF MS and HPLC significantly reduce the amount of biological material used for tests, but they require specialist equipment.

  10. Vibrational Spectroscopy of Methyl benzoate

    CERN Document Server

    Maiti, Kiran Sankar

    2014-01-01

    Methyl benzoate (MB) is studied as a model compound for the development of new IR pulse schemes with possible applicability to biomolecules. Anharmonic vibrational modes of MB are calculated on different level (MP2, SCS, CCSD(T) with varying basis sets) ab-initio PESs using the vibrational self-consistent field (VSCF) method and its correlation corrected extensions. Dual level schemes, combining different quantum chemical methods for diagonal and coupling potentials, are systematically studied and applied successfully to reduce the computational cost. Isotopic substitution of {\\beta}-hydrogen by deuterium is studied to obtain a better understanding of the molecular vibrational coupling topology.

  11. L-methionine degradation potentialities of cheese-ripening microorganisms.

    Science.gov (United States)

    Bonnarme, P; Lapadatescu, C; Yvon, M; Spinnler, H E

    2001-11-01

    Volatile sulphur compounds are major flavouring compounds in many traditional fermented foods including cheeses. These compounds are products of the catabolism of L-methionine by cheese-ripening microorganisms. The diversity of L-methionine degradation by such microorganisms, however, remains to be characterized. The objective of this work was to compare the capacities to produce volatile sulphur compounds by five yeasts, Geotrichum candidum, Yarrowia lipolytica, Kluyveromyces lactis, Debaryomyces hansenii, Saccharomyces cerevisiae and five bacteria, Brevibacterium linens, Corynebacterium glutamicum, Arthrobacter sp., Micrococcus lutens and Staphylococcus equorum of technological interest for cheese-ripening. The ability of whole cells of these microorganisms to generate volatile sulphur compounds from L-methionine was compared. The microorganisms produced a wide spectrum of sulphur compounds including methanethiol, dimethylsulfide, dimethyldisulfide, dimethyltrisulfide and also S-methylthioesters, which varied in amount and type according to strain. Most of the yeasts produced methanethiol, dimethylsulfide, dimethyldisulfide and dimethyltrisulfide but did not produce S-methylthioesters, apart from G. candidum that produced S-methyl thioacetate. Bacteria, especially Arth. sp. and Brevi. linens, produced the highest amounts and the greatest variety of volatile sulphur compounds includling methanethiol, sulfides and S-methylthioesters, e.g. S-methyl thioacetate, S-methyl thiobutyrate, S-methyl thiopropionate and S-methyl thioisovalerate. Cell-free extracts of all the yeasts and bacteria were examined for the activity of enzymes possibly involved in L-methionine catabolism, i.e. L-methionine demethiolase, L-methionine aminotransferase and L-methionine deaminase. They all possessed L-methionine demethiolase activity, while some (K. lactis, Deb. hansenii, Arth. sp., Staph. equorum) were deficient in L-methionine aminotransferase, and none produced L-methionine deaminase

  12. KINETICS STUDY ON NITRATION OF METHYL RICINOLEATE

    OpenAIRE

    Abdullah, Abdullah; Triyono, Triyono; Trisunaryanti, Wega; Haryadi, Winarto

    2012-01-01

    Kinetics parameter values of methyl ricinoleate nitration (rate constant, reaction order and the rate of reaction) have been determined. Nitration was carried out with both concentrations of HNO3 and acetic anhydride in excess to the concentration of methyl ricinoleate. Thus, the kinetics parameter value was only affected by the concentration of methyl ricinoleate. Based on kinetic study conducted, it could be concluded that the nitration follows pseudo first-order, and the reaction rate for ...

  13. Hypoxic radiosensitization by the antimicrobial methyl paraben

    Energy Technology Data Exchange (ETDEWEB)

    Jacobs, G.P.; Sade, N.

    1984-08-01

    The antimicrobial preservative, methyl paraben (methyl-4-hydroxybenzoate) sensitizes anoxic buffered suspensions of Staphylococcus aureus to gamma-radiation. The maximal response at an 0.5 mM concentration represents a 150 percent increase in response over that for deoxygenated suspensions without additive, and 80 percent of the response for aerated suspensions alone. Methyl paraben is not toxic to the test organism under the present test conditions.

  14. Distinct Methylation of IFNG in the Gut

    OpenAIRE

    Gonsky, Rivkah; Deem, Richard L; Targan, Stephan R.

    2009-01-01

    Mucosal expression of proinflammatory cytokines plays a pivotal role in inflammatory bowel disease (IBD) pathogenesis. Epigenetic remodeling of chromatin via DNA methylation regulates gene expression. In this study, IFNG DNA methylation was analyzed within the mucosal compartment in both normal and IBD populations and compared to its peripheral counterparts. Overall IFNG methylation (across eight CpG sites) was significantly lower in lamina propria (LP) T cells compared to peripheral blood (P...

  15. CCDC 1441885: Experimental Crystal Structure Determination : 5-t-butyl-2-(14-(4-t-butyl-2,6-diformylphenyl)-5,12-dimethyldibenzo[c,pqr]tetraphen-7-yl)isophthalaldehyde chloroform solvate

    KAUST Repository

    Zeng, Wangdong

    2016-01-01

    An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

  16. -coated nanostructures for dye photo-degradation in water

    Science.gov (United States)

    Scuderi, Viviana; Impellizzeri, Giuliana; Romano, Lucia; Scuderi, Mario; Nicotra, Giuseppe; Bergum, Kristin; Irrera, Alessia; Svensson, Bengt G.; Privitera, Vittorio

    2014-09-01

    The photocatalytic efficiency of a thin-film TiO2-coated nanostructured template is studied by dye degradation in water. The nanostructured template was synthesized by metal-assisted wet etching of Si and used as substrate for the deposition of a thin film of TiO2 (10 nm thick) by atomic layer deposition. A complete structural characterization was made by scanning and transmission electron microscopies. The significant photocatalytic performance was evaluated by the degradation of two dyes in water: methylene blue and methyl orange. The relevance of the reported results is discussed, opening the route toward the application of the synthesized nanostructured TiO2 for water purification.

  17. Research on Controllable Degradation of Novel Sulfonylurea Herbicides in Acidic and Alkaline Soils.

    Science.gov (United States)

    Zhou, Shaa; Hua, Xue-Wen; Wei, Wei; Gu, Yu-Cheng; Liu, Xiao-Qing; Chen, Jing-Huo; Chen, Ming-Gui; Xie, Yong-Tao; Zhou, Sha; Meng, Xiang-De; Zhang, Yan; Li, Yong-Hong; Wang, Bao-Lei; Song, Hai-Bin; Li, Zheng-Ming

    2017-09-06

    The degradation issue of sulfonylurea (SU) has become one of the biggest challenges that hamper the development and application of this class of herbicides, especially in the alkaline soils of northern China. On the basis of the previous discovery that some substituents on the fifth position of the benzene ring in Chlorsulfuron could hasten its degradation rate, apparently in acidic soil, this work on Metsulfuron-methyl showed more convincing results. Two novel compounds (I-1 and I-2) were designed and synthesized, and they still retained potent herbicidal activity in tests against both dicotyledons and monocotyledons. The half-lives of degradation (DT50) assay revealed that I-1 showed an accelerated degradation rate in acidic soil (pH 5.59). Moreover, we delighted to find that the degradation rate of I-1 was 9-10-fold faster than that of Metsulfuron-methyl and Chlorsulfuron when in alkaline soil (pH 8.46), which has more practical value. This research suggests that a modified structure that has potent herbicidal activity as well as accelerated degradation rate could be realized and this approach may provide a way to improve the residue problem of SUs in farmlands with alkaline soil.

  18. Synthesis and radiation degradation of vinyl polymers with fluorine: search for improved lithographic resists. [Gamma rays

    Energy Technology Data Exchange (ETDEWEB)

    Pittman, C.U. Jr. (Univ. of Alabama, University); Chen, C.Y.; Ueda, M.; Helbert, J.N.; Kwiatkowski, J.H.

    1980-12-01

    Homopolymers of methyl ..cap alpha..-fluoroacrylate (MFA), trifluoroethyl methacrylate (TFEM), and hexafluoroisopropyl methacrylate (HFIM) were prepared, as were their methyl methacrylate (MMA) copolymers. Copolymers of vinylidene fluoride (VDF) and chlorotrifluoroethylene (CTFE) with MMA were also prepared. The radiation susceptibilities of these polymers were measured by the /sup 60/Co ..gamma..-irradiation method, in which molecular weights were measured by membrane osmometry and gel permeation chromatography (GPC). All the copolymers degraded by predominant chain scission except poly(methyl ..cap alpha..-fluoroacrylate), (PMFA), which crosslinks even at low doses (ca. 1 Mrad). The G/sub s/-G/sub x/ and G/sub s/ values of the chain scissioning polymers and copolymers are higher than those of poly(methyl methacrylate) PMMA reference. The high susceptibility of PMFA homopolymer to crosslinking is in contrast to that of poly(methyl ..cap alpha..-chloroacrylate), as we reported earlier. This effect is interpreted as resulting from extensive hydrogen fluoride and polyenyl radical formation, which leads to facile crosslinking. However, incorporation of the MFA monomer unit causes the (22/78) MFA/MMA copolymer to degrade with a larger value of G/sub s/ that PMMA. Apparently a second-order process leads to crosslinking in PMFA and this is retarded in the copolymer. In the homopolymers of HFIM and TFEM and in the HFIM-MMA and TFEM-MMA copolymers the HFIM and TFEM components facilitate degradation with negligible crosslinking. The increased degradation susceptibility of VDF and CTFE copolymers with MMA over that of PMMA is attributed to processes at the VDF or CTFE components (present in smaller concentrations (3 to 5 mole %) than the threshold levels (25 to 50% necessary for significant crosslinking).

  19. Colorectal Cancer "Methylator Phenotype": Fact or Artifact?

    Directory of Open Access Journals (Sweden)

    Charles Anacleto

    2005-04-01

    Full Text Available It has been proposed that human colorectal tumors can be classified into two groups: one in which methylation is rare, and another with methylation of several loci associated with a "CpG island methylated phenotype (CIMP," characterized by preferential proximal location in the colon, but otherwise poorly defined. There is considerable overlap between this putative methylator phenotype and the well-known mutator phenotype associated with microsatellite instability (MSI. We have examined hypermethylation of the promoter region of five genes (DAPK, MGMT, hMLH1, p16INK4a, and p14ARF in 106 primary colorectal cancers. A graph depicting the frequency of methylated loci in the series of tumors showed a continuous, monotonically decreasing distribution quite different from the previously claimed discontinuity. We observed a significant association between the presence of three or more methylated loci and the proximal location of the tumors. However, if we remove from analysis the tumors with hMLH1 methylation or those with MSI, the significance vanishes, suggesting that the association between multiple methylations and proximal location was indirect due to the correlation with MSI. Thus, our data do not support the independent existence of the so-called methylator phenotype and suggest that it rather may represent a statistical artifact caused by confounding of associations.

  20. Flocculation of diatomite by methylated egg albumin.

    Science.gov (United States)

    Seki, Hideshi; Suzuki, Akira

    2003-07-01

    A common and inexpensive protein, egg albumin, was applied to the solid-liquid separation or flocculation of diatomite. Egg albumin was methylated in a 0.05 M HCl methyl alcohol solution at room temperature. About 90% of the carboxylic groups of egg albumin could be methylated within 24 h. The adsorption of egg albumin onto diatomite at pH 6.8 was remarkably enhanced by methylation. The adsorption constant of methylated egg albumin to diatomite at 30 degrees C was about 100-fold larger than that of native egg albumin; however, the adsorption constant of methylated egg albumin decreased to about 1/100 with temperature decreasing from 30 to 6 degrees C. The saturated adsorption amount of egg albumin was also increased by the methylation. The flocculating ability of methylated egg albumin was examined with a diatomite suspension at 6 and 30 degrees C in the pH range from pH 2 to 11. The diatomite suspension was effectively flocculated by the addition of small amounts of methylated egg albumin (only 0.5-1 wt% against diatomite) over a wide pH range from pH 3 to 10.

  1. Influence of DNA methylation on transgene expression

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    DNA methylation plays an important role in gene expression in eukaryote. But DNA methylation of transgene usually leads to target gene silencing in plant genetic engineering. In this research, reporter gene b-glu- curonidase (GUS) gene (uidA) was introduced into tobaccos via Agrobacterium-mediated transformation method, and the foreign uidA gene became inactive in some transgenic tobaccos. No mRNA of uidA was detected in these plants by Northern blotting analysis, and DNA methylation of promoter region was found. The results indicated that gene silencing might be caused by DNA methylation of promoter.

  2. Daylight-driven photocatalytic degradation of ionic dyes with negatively surface-charged In2S3 nanoflowers: dye charge-dependent roles of reactive species

    Science.gov (United States)

    Ge, Suxiang; Cai, Lejuan; Li, Dapeng; Fa, Wenjun; Zhang, Yange; Zheng, Zhi

    2015-12-01

    Even though dye degradation is a successful application of semiconductor photocatalysis, the roles of reactive species in dye degradation have not received adequate attention. In this study, we systematically investigated the degradation of two cationic dyes (rhodamine B and methylene blue) and two anionic dyes (methyl orange and orange G) over negatively surface-charged In2S3 nanoflowers synthesized at 80 °C under indoor daylight lamp irradiation. It is notable to find In2S3 nanoflowers were more stable in anionic dyes degradation compared to that in cationic dyes removal. The active species trapping experiments indicated photogenerated electrons were mainly responsible for cationic dyes degradation, but holes were more important in anionic dyes degradation. A surface-charge-dependent role of reactive species in ionic dye degradation was proposed for revealing such interesting phenomenon. This study would provide a new insight for preparing highly efficient daylight-driven photocatalyst for ionic dyes degradation.

  3. Kresoxim methyl dissipation kinetics and its residue effect on soil extra-cellular and intra-cellular enzymatic activity in four different soils of India.

    Science.gov (United States)

    Sabale, Rupali P; Shabeer T P, Ahammed; Utture, Sagar C; Banerjee, Kaushik; Oulkar, Dasharath P; Adsule, Pandurang G; Deshmukh, Madhukar B

    2015-01-01

    The rate of degradation of kresoxim methyl and its effect on soil extra-cellular (acid phosphatase, alkaline phosphatase and β-glucosidase) and intra-cellular (dehydrogenase) enzymes were explored in four different soils of India. In all the tested soils, the degradation rate was faster at the beginning, which slowed down with time indicating a non-linear pattern of degradation. Rate of degradation in black soil was fastest followed by saline, brown and red soils, respectively and followed 1st or 1st + 1st order kinetics with half-life ranging between 1-6 days for natural soil and 1-19 days for sterile soils. The rate of degradation in natural against sterilized soils suggests that microbial degradation might be the major pathway of residue dissipation. Although small changes in enzyme activities were observed, kresoxim methyl did not have any significant deleterious effect on the enzymatic activity of the various test soils in long run. Simple correlation studies between degradation percentage and individual enzyme activities did not establish any significant relationships. The pattern and change of enzyme activity was primarily due to the effect of the incubation period rather than the effect of kresoxim methyl itself.

  4. Methylation diet and methyl group genetics in risk for adenomatous polyp occurrence

    Directory of Open Access Journals (Sweden)

    Mark Lucock

    2015-06-01

    Conclusion: A methylation diet influences methyl group synthesis in the regulation of blood homocysteine level, and is modulated by genetic interactions. Methylation-related nutrients also interact with key genes to modify risk of AP, a precursor of colorectal cancer. Independent of diet, two methylation-related genes (A2756G-MS and A66G-MSR were directly associated with AP occurrence.

  5. Chiral methyl-branched pheromones.

    Science.gov (United States)

    Ando, Tetsu; Yamakawa, Rei

    2015-07-01

    Insect pheromones are some of the most interesting natural products because they are utilized for interspecific communication between various insects, such as beetles, moths, ants, and cockroaches. A large number of compounds of many kinds have been identified as pheromone components, reflecting the diversity of insect species. While this review deals only with chiral methyl-branched pheromones, the chemical structures of more than one hundred non-terpene compounds have been determined by applying excellent analytical techniques. Furthermore, their stereoselective syntheses have been achieved by employing trustworthy chiral sources and ingenious enantioselective reactions. The information has been reviewed here not only to make them available for new research but also to understand the characteristic chemical structures of the chiral pheromones. Since biosynthetic studies are still limited, it might be meaningful to examine whether the structures, particularly the positions and configurations of the branched methyl groups, are correlated with the taxonomy of the pheromone producers and also with the function of the pheromones in communication systems.

  6. Strategies to decolorize high concentrations of methyl orange using growing cells of Lactobacillus casei TISTR 1500.

    Science.gov (United States)

    Tantiwa, Nidtaya; Seesuriyachan, Phisit; Kuntiya, Ampin

    2013-01-01

    Batch, fed-batch, and continuous fermentation was used in the processing of methyl orange decolorization using growing cells of Lactobacillus casei TISTR 1500. This report presents the optimal conditions for methyl orange decolorization by the strain TISTR 1500 in modified MRS via a central composite design (CCD) experiment. In particular, the highest decolorization efficiencies were obtained with 13.41 g/L of meat extract, and with 10.89 g/L of yeast extract at pH 6.88 at 35 °C. Under the optimal conditions, the rate of decolorization increased to 322% of that obtained for un-optimized MRS medium. The high concentration of methyl orange (5 g/L) was completely degraded within 9 h in batch fermentation. The total methyl orange load with 8.075 g/L was also decolorized in fed-batch fermentation within 13 h, and the biomass of the strain dramatically decreased after an incubation time of 8 h due to a shortage of sucrose. In the continuous system with a dye-loading rate of 600 mg/L/h and a total of loaded azo dye of 7.2 g/L, high efficiency of methyl orange removal was significantly high, at 98%.

  7. Degradation mechanisms of geosmin and 2-MIB during UV photolysis and UV/chlorine reactions.

    Science.gov (United States)

    Kim, Tae-Kyoung; Moon, Bo-Ram; Kim, Taeyeon; Kim, Moon-Kyung; Zoh, Kyung-Duk

    2016-11-01

    We conducted chlorination, UV photolysis, and UV/chlorin reactions to investigate the intermediate formation and degradation mechanisms of geosmin and 2-methylisoborneol (2-MIB) in water. Chlorination hardly removed geosmin and 2-MIB, while the UV/chlorine reaction at 254 nm completely removed geosmin and 2-MIB within 40 min and 1 h, respectively, with lesser removals of both compounds during UV photolysis. The kinetics during both UV photolysis and UV/chlorine reactions followed a pseudo first-order reaction. Chloroform was found as a chlorinated intermediate during the UV/chlorine reaction of both geosmin and 2-MIB. The pH affected both the degradation and chloroform production during the UV/chlorine reaction. The open ring and dehydration intermediates identified during UV/chlorine reactions were 1,4-dimethyl-adamantane, and 1,3-dimethyl-adamantane from geosmin, 2-methylenebornane, and 2-methyl-2-bornene from 2-MIB, respectively. Additionally, 2-methyl-3-pentanol, 2,4-dimethyl-1-heptene, 4-methyl-2-heptanone, and 1,1-dichloro-2,4-dimethyl-1-heptane were newly identified intermediates from UV/chlorine reactions of both geosmin and 2-MIB. These intermediates were degraded as the reaction progressed. We proposed possible degradation pathways during the UV photolysis and UV/chlorine reactions of both compounds using the identified intermediates.

  8. Thermal battery degradation mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Missert, Nancy A. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Brunke, Lyle Brent [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2015-09-01

    Diffuse reflectance IR spectroscopy (DRIFTS) was used to investigate the effect of accelerated aging on LiSi based anodes in simulated MC3816 batteries. DRIFTS spectra showed that the oxygen, carbonate, hydroxide and sulfur content of the anodes changes with aging times and temperatures, but not in a monotonic fashion that could be correlated to phase evolution. Bands associated with sulfur species were only observed in anodes taken from batteries aged in wet environments, providing further evidence for a reaction pathway facilitated by H2S transport from the cathode, through the separator, to the anode. Loss of battery capacity with accelerated aging in wet environments was correlated to loss of FeS2 in the catholyte pellets, suggesting that the major contribution to battery performance degradation results from loss of active cathode material.

  9. A genome-wide methylation study on obesity Differential variability and differential methylation

    NARCIS (Netherlands)

    Xu, Xiaojing; Su, Shaoyong; Barnes, Vernon A.; De Miguel, Carmen; Pollock, Jennifer; Ownby, Dennis; Shi, Huidong; Zhu, Haidong; Snieder, Harold; Wang, Xiaoling

    2013-01-01

    Besides differential methylation, DNA methylation variation has recently been proposed and demonstrated to be a potential contributing factor to cancer risk. Here we aim to examine whether differential variability in methylation is also an important feature of obesity, a typical non-malignant common

  10. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Science.gov (United States)

    2010-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF...: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.2000 Vinylidene chloride/methyl acrylate/methyl methacrylate polymers. The vinylidene chloride/methyl...

  11. A genome-wide methylation study on obesity Differential variability and differential methylation

    NARCIS (Netherlands)

    Xu, Xiaojing; Su, Shaoyong; Barnes, Vernon A.; De Miguel, Carmen; Pollock, Jennifer; Ownby, Dennis; Shi, Huidong; Zhu, Haidong; Snieder, Harold; Wang, Xiaoling

    2013-01-01

    Besides differential methylation, DNA methylation variation has recently been proposed and demonstrated to be a potential contributing factor to cancer risk. Here we aim to examine whether differential variability in methylation is also an important feature of obesity, a typical non-malignant common

  12. New primers for methylation-specific polymerase chain reaction enhance specificity of detecting STAT1 methylation

    Directory of Open Access Journals (Sweden)

    Ming-Cheng Chang

    2012-03-01

    Conclusion: Specific primers for methylation-specific PCR are mandatory for the accurate detection of STAT1 gene methylation. Besides, specific primers can generate correct interpretation of STAT1 gene methylation, and its correlation with the clinicopathological characteristics and outcome of cancer patients.

  13. Structural analysis of the O-polysaccharide of the lipopolysaccharide from Azospirillum brasilense Jm6B2 containing 3-O-methyl-D-rhamnose (D-acofriose).

    Science.gov (United States)

    Boyko, Alevtina S; Dmitrenok, Andrey S; Fedonenko, Yuliya P; Zdorovenko, Evelina L; Konnova, Svetlana A; Knirel, Yuriy A; Ignatov, Vladimir V

    2012-07-01

    Two types of neutral O-polysaccharides were obtained by mild acid degradation of the lipopolysaccharide isolated by phenol-water extraction from the asymbiotic diazotrophic rhizobacterium Azospirillum brasilense Jm6B2. The following structure of the major O-polysaccharide was established by composition and methylation (ethylation) analyses, Smith degradation, and 1D and 2D (1)H and (13)C NMR spectroscopy: [structure: see text] where a non-stoichiometric (~60%) 3-O-methylation of D-rhamnose is indicated by italics.

  14. DEGRADATION OF SHAPE MEMORY EFFECT

    OpenAIRE

    VanderMeer, R.

    1982-01-01

    An important parameter for deciding whether or not a SME alloy is suitable for practical applications is the magnitude of the strain reversa1 accompanying martensite reversion. This research is concerned with elucidating metallurgical factors that cause degradation of this heat-activated recovery strain, ER. After explaining what is meant by degradation, two manifestations of degradation recently identified in near-monotectoid uranium-niobium alloys will be described. The first was associated...

  15. Synthesis of ribosomal proteins in developing Dictyostelium discoideum cells is controlled by the methylation of proteins S24 and S31.

    Science.gov (United States)

    Mangiarotti, Giorgio

    2002-01-01

    Ribosomal protein mRNAs left over from growth are selectively excluded from polyribosomes in the first half of Dictyostelium discoideum development. This is due to the fact that they are sequestered by a class of free 40S ribosomal subunits, characterized by possessing a methylated S24 protein. At the time of formation of tight cell aggregates, the methylated S24 is substituted by an unmethylated S24, while protein S31 of the same or other 40S subunits becomes methylated. This leads to a rapid degradation of the ribosomal protein mRNAs.

  16. Transcellular degradation of axonal mitochondria.

    Science.gov (United States)

    Davis, Chung-ha O; Kim, Keun-Young; Bushong, Eric A; Mills, Elizabeth A; Boassa, Daniela; Shih, Tiffany; Kinebuchi, Mira; Phan, Sebastien; Zhou, Yi; Bihlmeyer, Nathan A; Nguyen, Judy V; Jin, Yunju; Ellisman, Mark H; Marsh-Armstrong, Nicholas

    2014-07-01

    It is generally accepted that healthy cells degrade their own mitochondria. Here, we report that retinal ganglion cell axons of WT mice shed mitochondria at the optic nerve head (ONH), and that these mitochondria are internalized and degraded by adjacent astrocytes. EM demonstrates that mitochondria are shed through formation of large protrusions that originate from otherwise healthy axons. A virally introduced tandem fluorophore protein reporter of acidified mitochondria reveals that acidified axonal mitochondria originating from the retinal ganglion cell are associated with lysosomes within columns of astrocytes in the ONH. According to this reporter, a greater proportion of retinal ganglion cell mitochondria are degraded at the ONH than in the ganglion cell soma. Consistently, analyses of degrading DNA reveal extensive mtDNA degradation within the optic nerve astrocytes, some of which comes from retinal ganglion cell axons. Together, these results demonstrate that surprisingly large proportions of retinal ganglion cell axonal mitochondria are normally degraded by the astrocytes of the ONH. This transcellular degradation of mitochondria, or transmitophagy, likely occurs elsewhere in the CNS, because structurally similar accumulations of degrading mitochondria are also found along neurites in superficial layers of the cerebral cortex. Thus, the general assumption that neurons or other cells necessarily degrade their own mitochondria should be reconsidered.

  17. Aerobic degradation of polychlorinated biphenyls

    Energy Technology Data Exchange (ETDEWEB)

    Pieper, D.H. [Dept. of Environmental Microbiology, German Research Center for Biotechnology, Braunschweig (Germany)

    2005-04-01

    The microbial degradation of polychlorinated biphenyls (PCBs) has been extensively studied in recent years. The genetic organization of biphenyl catabolic genes has been elucidated in various groups of microorganisms, their structures have been analyzed with respect to their evolutionary relationships, and new information on mobile elements has become available. Key enzymes, specifically biphenyl 2,3-dioxygenases, have been intensively characterized, structure/sequence relationships have been determined and enzymes optimized for PCB transformation. However, due to the complex metabolic network responsible for PCB degradation, optimizing degradation by single bacterial species is necessarily limited. As PCBs are usually not mineralized by biphenyl-degrading organisms, and cometabolism can result in the formation of toxic metabolites, the degradation of chlorobenzoates has received special attention. A broad set of bacterial strategies to degrade chlorobenzoates has recently been elucidated, including new pathways for the degradation of chlorocatechols as central intermediates of various chloroaromatic catabolic pathways. To optimize PCB degradation in the environment beyond these metabolic limitations, enhancing degradation in the rhizosphere has been suggested, in addition to the application of surfactants to overcome bioavailability barriers. However, further research is necessary to understand the complex interactions between soil/sediment, pollutant, surfactant and microorganisms in different environments. (orig.)

  18. CCDC 900612: Experimental Crystal Structure Determination : (4,4'-Di-t-butyl-2,2'-bipyridine)-trifluoromethanethiolato-copper

    KAUST Repository

    Weng, Zhiqiang

    2013-01-01

    An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

  19. UV absorption spectra, kinetics and mechanism for alkyl and alkyl peroxy radicals originating from t-butyl alcohol

    DEFF Research Database (Denmark)

    Langer, S.; Ljungström, E.; Sehested, J.

    1994-01-01

    Alkyl and alkyl peroxy radicals from 1-butyl alcohol (TBA), HOC (CH3)2CH2. and HOC(CH3)2CH2O2. have been studied in the ps phase at 298 K. Two techniques were used: pulse radiolysis UV absorption to measure the spectra and kinetics, and long path-length Fourier transform infrared spectroscopy (FTIR......) to identify and quantify the reaction products. Absorption cross sections were quantified over the wavelength range 220-320 nm. At 240 nm, sigma(HOC(CH3)2CH2) = (2.4 +/- 0.3) x 10(-18) and sigma(HOC(CH3)2CH2O2) = (3.4 +/- 0.5) X 10(-18) cm2 molecule-1 have been obtained. Observed rate constants for the self...

  20. Contribution of ethylamine degrading bacteria to atrazine degradation in soils.

    Science.gov (United States)

    Smith, Daniel; Crowley, David E

    2006-11-01

    Bacterial communities that cooperatively degrade atrazine commonly consist of diverse species in which the genes for atrazine dechlorination and dealkylation are variously distributed among different species. Normally, the first step in degradation of atrazine involves dechlorination mediated by atzA, followed by stepwise dealkylation to yield either N-ethylammelide or N-isopropylammelide. As the liberated alkylamine moieties are constituents of many organic molecules other than atrazine, it is possible that a large number of alkylamine-degrading bacteria other than those previously described might contribute to this key step in atrazine degradation. To examine this hypothesis, we isolated 82 bacterial strains from soil by plating soil water extracts on agar media with ethylamine as a sole carbon source. Among the relatively large number of isolates, only 3 were able to degrade N-ethylammelide, and in each case were shown to carry the atzB gene and atzC genes. The isolates, identified as Rhizobium leguminosarum, Flavobacterium sp., and Arthrobacter sp., were all readily substituted into an atrazine-degrading consortium to carry out N-ethylammelide degradation. The distribution of these genes among many different species in the soil microbial population suggests that these genes are highly mobile and over time may lead to generation of various atrazine-degrading consortia.

  1. Methylation Linear Discriminant Analysis (MLDA for identifying differentially methylated CpG islands

    Directory of Open Access Journals (Sweden)

    Vass J Keith

    2008-08-01

    Full Text Available Abstract Background Hypermethylation of promoter CpG islands is strongly correlated to transcriptional gene silencing and epigenetic maintenance of the silenced state. As well as its role in tumor development, CpG island methylation contributes to the acquisition of resistance to chemotherapy. Differential Methylation Hybridisation (DMH is one technique used for genome-wide DNA methylation analysis. The study of such microarray data sets should ideally account for the specific biological features of DNA methylation and the non-symmetrical distribution of the ratios of unmethylated and methylated sequences hybridised on the array. We have therefore developed a novel algorithm tailored to this type of data, Methylation Linear Discriminant Analysis (MLDA. Results MLDA was programmed in R (version 2.7.0 and the package is available at CRAN 1. This approach utilizes linear regression models of non-normalised hybridisation data to define methylation status. Log-transformed signal intensities of unmethylated controls on the microarray are used as a reference. The signal intensities of DNA samples digested with methylation sensitive restriction enzymes and mock digested are then transformed to the likelihood of a locus being methylated using this reference. We tested the ability of MLDA to identify loci differentially methylated as analysed by DMH between cisplatin sensitive and resistant ovarian cancer cell lines. MLDA identified 115 differentially methylated loci and 23 out of 26 of these loci have been independently validated by Methylation Specific PCR and/or bisulphite pyrosequencing. Conclusion MLDA has advantages for analyzing methylation data from CpG island microarrays, since there is a clear rational for the definition of methylation status, it uses DMH data without between-group normalisation and is less influenced by cross-hybridisation of loci. The MLDA algorithm successfully identified differentially methylated loci between two classes of

  2. Methylation of inorganic mercury in polar marine waters

    Science.gov (United States)

    Lehnherr, Igor; St. Louis, Vincent L.; Hintelmann, Holger; Kirk, Jane L.

    2011-05-01

    Monomethylmercury is a neurotoxin that accumulates in marine organisms, with serious implications for human health. The toxin is of particular concern to northern Inuit peoples, for example, whose traditional diets are composed primarily of marine mammals and fish. The ultimate source of monomethylmercury to marine organisms has remained uncertain, although various potential sources have been proposed, including export from coastal and deep-sea sediments and major river systems, atmospheric deposition and water-column production. Here, we report results from incubation experiments in which we added isotopically labelled inorganic mercury and monomethylmercury to seawater samples collected from a range of sites in the Canadian Arctic Archipelago. Monomethylmercury formed from the methylation of inorganic mercury in all samples. Demethylation of monomethylmercury was also observed in water from all sites. We determined steady-state concentrations of monomethylmercury in marine waters by incorporating the rate constants for monomethylmercury formation and degradation derived from these experiments into a numerical model. We estimate that the conversion of inorganic mercury to monomethylmercury in the water column accounts for around 47% (+/-62%, standard deviation) of the monomethylmercury present in polar marine waters, with site-to-site differences in inorganic mercury and monomethylmercury levels accounting for most of the variability. We suggest that water-column methylation of inorganic mercury is a significant source of monomethylmercury in pelagic marine food webs in the Arctic, and possibly in the world's oceans in general.

  3. Numerical modelling of methyl iodide in the eastern tropical Atlantic

    Directory of Open Access Journals (Sweden)

    I. Stemmler

    2013-06-01

    Full Text Available Methyl iodide (CH3I is a volatile organic halogen compound that contributes significantly to the transport of iodine from the ocean to the atmosphere, where it plays an important role in tropospheric chemistry. CH3I is naturally produced and occurs in the global ocean. The processes involved in the formation of CH3I, however, are not fully understood. In fact, there is an ongoing debate whether production by phytoplankton or photochemical degradation of organic matter is the main source term. Here, both the biological and photochemical production mechanisms are considered in a biogeochemical module that is coupled to a one-dimensional water column model for the eastern tropical Atlantic. The model is able to reproduce observed subsurface maxima of CH3I concentrations. But, the dominating source process cannot be clearly identified as subsurface maxima can occur due to both direct biological and photochemical production. However, good agreement between the observed and simulated difference between surface and subsurface methyl iodide concentrations is achieved only when direct biological production is taken into account. Production rates for the biological CH3I source that were derived from published laboratory studies are shown to be inappropriate for explaining CH3I concentrations in the eastern tropical Atlantic.

  4. Regulation of small RNA stability: methylation and beyond

    Institute of Scientific and Technical Information of China (English)

    Lijuan Ji; Xuemei Chen

    2012-01-01

    As central components of RNA silencing,small RNAs play diverse and important roles in many biological processes in eukaryotes.Aberrant reduction or elevation in the levels of small RNAs is associated with many developmental and physiological defects.The in vivo levels of small RNAs are precisely regulated through modulating the rates of their biogenesis and turnover.2'-O-methylation on the 3' terminal ribose is a major mechanism that increases the stability of small RNAs.The small RNA methyltransferase HUA ENHANCER1 (HEN1) and its homologs methylate microRNAs and small interfering RNAs (siRNAs) in plants,Piwi-interacting RNAs (piRNAs) in animals,and siRNAs in Drosophila.3' nucleotide addition,especially uridylation,and 3'-5' exonucleolytic degradation are major mechanisms that turnover small RNAs.Other mechanisms impacting small RNA stability include complementary RNAs,cis-elements in small RNA sequences and RNA-binding proteins.Investigations are ongoing to further understand how small RNA stability impacts their accumulation in vivo in order to improve the utilization of RNA silencing in biotechnology and therapeutic applications.

  5. Research of Isolation and Degradation Conditions of Petroleum Degrading Marine

    Science.gov (United States)

    Fangrui, Guo

    2017-01-01

    A novel petroleum-degrading microbial strain was isolated from sediment samples in estuary of Bohai Sea estuary beaches. The strain was primarily identified as Alcanivorax sp. and named Alcanivorax sp. H34. Effect of PH values, temperature, nitrogen and phosphorus concentrations on degradation of H34 were investigated. The paraffinic components average degradation rate of H34 ungrowth cells under optimized conditions was studied. The results showed that the optimal growth conditions of H34 are were temperature of 30°C, initial PH of 7.0, nitrogen concentration of 3g/L, phosphorus concentration of 3g/L, and paraffinic components average degradation rates of H34 ungrowth cells was 41.6%, while total degradation rate was 45.5%.

  6. Electrochemical biosensing strategies for DNA methylation analysis.

    Science.gov (United States)

    Hossain, Tanvir; Mahmudunnabi, Golam; Masud, Mostafa Kamal; Islam, Md Nazmul; Ooi, Lezanne; Konstantinov, Konstantin; Hossain, Md Shahriar Al; Martinac, Boris; Alici, Gursel; Nguyen, Nam-Trung; Shiddiky, Muhammad J A

    2017-02-17

    DNA methylation is one of the key epigenetic modifications of DNA that results from the enzymatic addition of a methyl group at the fifth carbon of the cytosine base. It plays a crucial role in cellular development, genomic stability and gene expression. Aberrant DNA methylation is responsible for the pathogenesis of many diseases including cancers. Over the past several decades, many methodologies have been developed to detect DNA methylation. These methodologies range from classical molecular biology and optical approaches, such as bisulfite sequencing, microarrays, quantitative real-time PCR, colorimetry, Raman spectroscopy to the more recent electrochemical approaches. Among these, electrochemical approaches offer sensitive, simple, specific, rapid, and cost-effective analysis of DNA methylation. Additionally, electrochemical methods are highly amenable to miniaturization and possess the potential to be multiplexed. In recent years, several reviews have provided information on the detection strategies of DNA methylation. However, to date, there is no comprehensive evaluation of electrochemical DNA methylation detection strategies. Herein, we address the recent developments of electrochemical DNA methylation detection approaches. Furthermore, we highlight the major technical and biological challenges involved in these strategies and provide suggestions for the future direction of this important field.

  7. DNA Methylation Modulates Nociceptive Sensitization after Incision.

    Directory of Open Access Journals (Sweden)

    Yuan Sun

    Full Text Available DNA methylation is a key epigenetic mechanism controlling DNA accessibility and gene expression. Blockade of DNA methylation can significantly affect pain behaviors implicated in neuropathic and inflammatory pain. However, the role of DNA methylation with regard to postoperative pain has not yet been explored. In this study we sought to investigate the role of DNA methylation in modulating incisional pain and identify possible targets under DNA methylation and contributing to incisional pain. DNA methyltranferase (DNMT inhibitor 5-Aza-2'-deoxycytidine significantly reduced incision-induced mechanical allodynia and thermal sensitivity. Aza-2'-deoxycytidine also reduced hindpaw swelling after incision, suggesting an anti-inflammatory effect. Global DNA methylation and DNMT3b expression were increased in skin after incision, but none of DNMT1, DNMT3a or DNMT3b was altered in spinal cord or DRG. The expression of proopiomelanocortin Pomc encoding β-endorphin and Oprm1 encoding the mu-opioid receptor were upregulated peripherally after incision; moreover, Oprm1 expression was further increased under DNMT inhibitor treatment. Finally, local peripheral injection of the opioid receptor antagonist naloxone significantly exacerbated incision-induced mechanical hypersensitivity. These results suggest that DNA methylation is functionally relevant to incisional nociceptive sensitization, and that mu-opioid receptor signaling might be one methylation regulated pathway controlling sensitization after incision.

  8. Adenine N6-methylation in diverse fungi

    NARCIS (Netherlands)

    Seidl, Michael F.

    2017-01-01

    A DNA modification - methylation of cytosines and adenines - has important roles in diverse processes such as regulation of gene expression and genome stability, yet until recently adenine methylation had been considered to be only a hallmark of prokaryotes. A new study identifies abundant

  9. mCCG methylation in angiosperms.

    Science.gov (United States)

    Jeddeloh, J A; Richards, E J

    1996-05-01

    Two different methods were used to investigate the abundance of cytosine methylation at the outer (5') position in 5'-CCG-3' trinucleotides in angiosperm genomes. Mspl is unable to cut its target site if the outer cytosine is methylated (5'-mCCGG-3'). Using Mspl restriction analysis, it was shown that 5'-mCCG-3' is present in all angiosperm genomes examined, and that the amount of cytosine methylation at this site varies between species. Subsequently, direct measurements were made of the amount of methylation at both cytosines in a subset of 5'-CCG-3' trinucleotides in the Arabidopsis thaliana genome. Based upon these analyses, it was estimated that approximately 20-30% of 5'-CCG-3' trinucleotides in A. thaliana are methylated at the outer cytosine. Approximately 20% of the 5'-CCG-3' trinucleotides contain 5-methyl-cytosine at the inner cytosine position, which corresponds to a previous determination of 5'-mCG-3' methylation in A. thaliana. The implications of 5'-mCCG-3' methylation are discussed.

  10. Phytoestrogens in the environment, II: microbiological degradation of phytoestrogens and the response of fathead minnows to degradate exposure.

    Science.gov (United States)

    Kelly, Megan M; Fleischhacker, Nathan T; Rearick, Daniel C; Arnold, William A; Schoenfuss, Heiko L; Novak, Paige J

    2014-03-01

    Phytoestrogens are endocrine active compounds derived from plants, including the isoflavones genistein and daidzein, and their methylated derivatives biochanin A and formononetin. These compounds have been detected at the µg/L level in the effluents of plant-processing industries and municipal treatment plants and at the ng/L level in surface waters worldwide. The present study assessed the persistence of genistein and daidzein in natural aquatic systems, specifically riverine samples. Initial concentration, temperature, sample location, and time of sample collection varied. Genistein and daidzein were found to be readily biodegradable at all tested concentrations, at both 10 °C and 20 °C, in samples collected during different seasons, and in samples from 3 different rivers. In addition, organismal responses in larval and sexually mature fathead minnows (Pimephales promelas) were quantified following exposure to microbiologically degraded phytoestrogens (genistein, daidzein, and formononetin). Products of the microbiological degradation of parent phytoestrogens did not affect larval survival, growth, or predator avoidance. Female adult fathead minnows exposed to these degradation products produced significantly fewer eggs than those exposed to a control, but no other morphological, physiological, or behavioral changes were observed with male or female minnows. The present research suggests that although phytoestrogens are not likely to persist in aquatic systems, they may pseudo-persist if discharges are continuous; in addition, caution should be exercised with respect to high-concentration effluents because of the potentially antiestrogenic effects of phytoestrogen degradates.

  11. Enhanced photodegradation of methyl orange with TiO2 nanoparticles using a triboelectric nanogenerator

    Science.gov (United States)

    Su, Yuanjie; Yang, Ya; Zhang, Hulin; Xie, Yannan; Wu, Zhiming; Jiang, Yadong; Fukata, Naoki; Bando, Yoshio; Wang, Zhong Lin

    2013-07-01

    Methyl orange (MO) can be degraded by a photocatalytic process using TiO2 under UV irradiation. The photo-generated holes and electrons can migrate to the surface of TiO2 particles and serve as redox sources that react with adsorbed reactants, leading to the formation of superoxide radical anions, hydrogen peroxide and hydroxyl radicals involved in the oxidation of dye pollution. Here, we fabricated a polytetrafluoroethylene-Al based triboelectric nanogenerator (TENG) whose electric power output can be used for enhancing the photodegradation of MO with the presence of TiO2 nanoparticles, because the TENG generated electric field can effectively boost the separation and restrain the recombination of photo-generated electrons and holes. Due to the photoelectrical coupling, the degradation percentages of MO for 120 min with and without TENG assistance are 76% and 27%, respectively. The fabricated TENGs have potential applications in wastewater treatment, water splitting, and pollution degradation.

  12. Clay and Soil Photolysis of the Pesticides Mesotrione and Metsulfuron Methyl

    Directory of Open Access Journals (Sweden)

    Marie Siampiringue

    2014-01-01

    Full Text Available Photolysis may represent an important degradation process of pollutants at the surface of soil. In the present work, we report a detailed study on the degradation of two pesticides: mesotrione and metsulfuron methyl using a sunlight simulator. In a first step, we studied the photochemical behaviour at the surface of clays from the kinetic as well as from the analytical point of view. In both cases, the quantum yields were found to be higher when compared to those obtained in aqueous solutions. The effect of iron(III, water, and humic substances contents was studied. In the former cases, an increase of the degradation rate was observed while an inhibition was observed with the latter owing to a filter effect phenomenon. In a second step, we studied the photodegradation at the surface of natural soil and identified the generated byproducts. They appear to mainly arise from photohydrolysis process.

  13. Turning over DNA methylation in the mind

    Directory of Open Access Journals (Sweden)

    Ryan eLister

    2015-07-01

    Full Text Available Cytosine DNA methylation is a stable epigenetic modification with established roles in regulating transcription, imprinting, female X-chromosome inactivation, and silencing of transposons. Dynamic gain or loss of DNA methylation reshapes the genomic landscape of cells during early differentiation, and in post-mitotic mammalian brain cells these changes continue to accumulate throughout the phases of cortical maturation in childhood and adolescence. There is also evidence for dynamic changes in the methylation status of specific genomic loci during the encoding of new memories, and these epigenome dynamics could play a causal role in memory formation. However, the mechanisms that may dynamically regulate DNA methylation in neurons during memory formation and expression, and the function of such epigenomic changes in this context, are unclear. Here we discuss the possible roles of DNA methylation in encoding and retrieval of memory.

  14. CG methylation in DNA transcription

    Science.gov (United States)

    Chela-Flores, J.; Migoni, R. L.

    1990-08-01

    A simple model of DNA is considered in which the nucleotides cytosine (C) and guanine (G) are not assumed to be identical, and in which macroscopic thermodynamic quantities may be calculated exactly. The H bonds between the C and G nucleotides are assumed to be Morse potentials. We discuss the statistical mechanics of the DNA molecule in the configuration (5'...GGG ...3'; 3'...CCC ...5'), which may be copied by RNA polymerase into a messenger RNA (mRNA) strand (5'...CCC ...3'). This model suggests that replacements of C by 5-methylcytosine (5mC) may be a secondary effect in the inhibition of genetic expression, not interfering directly with the formation of an open state. An experimental test is suggested. The implications of this result are discussed for a related system, in which the enzyme methylase is known to methylate almost exclusively those Cs that are followed by Gs as a regulatory strategy employed by some eukaryotes.

  15. DNA sequence explains seemingly disordered methylation levels in partially methylated domains of Mammalian genomes.

    Directory of Open Access Journals (Sweden)

    Dimos Gaidatzis

    2014-02-01

    Full Text Available For the most part metazoan genomes are highly methylated and harbor only small regions with low or absent methylation. In contrast, partially methylated domains (PMDs, recently discovered in a variety of cell lines and tissues, do not fit this paradigm as they show partial methylation for large portions (20%-40% of the genome. While in PMDs methylation levels are reduced on average, we found that at single CpG resolution, they show extensive variability along the genome outside of CpG islands and DNase I hypersensitive sites (DHS. Methylation levels range from 0% to 100% in a roughly uniform fashion with only little similarity between neighboring CpGs. A comparison of various PMD-containing methylomes showed that these seemingly disordered states of methylation are strongly conserved across cell types for virtually every PMD. Comparative sequence analysis suggests that DNA sequence is a major determinant of these methylation states. This is further substantiated by a purely sequence based model which can predict 31% (R(2 of the variation in methylation. The model revealed CpG density as the main driving feature promoting methylation, opposite to what has been shown for CpG islands, followed by various dinucleotides immediately flanking the CpG and a minor contribution from sequence preferences reflecting nucleosome positioning. Taken together we provide a reinterpretation for the nucleotide-specific methylation levels observed in PMDs, demonstrate their conservation across tissues and suggest that they are mainly determined by specific DNA sequence features.

  16. Microbial surfactant mediated degradation of anthracene in aqueous phase by marine Bacillus licheniformis MTCC 5514

    Directory of Open Access Journals (Sweden)

    Sreethar Swaathy

    2014-12-01

    Full Text Available The present study emphasizes the biosurfactant mediated anthracene degradation by a marine alkaliphile Bacillus licheniformis (MTCC 5514. The isolate, MTCC 5514 degraded >95% of 300 ppm anthracene in an aqueous medium within 22 days and the degradation percentage reduced significantly when the concentration of anthracene increased to above 500 ppm. Naphthalene, naphthalene 2-methyl, phthalic acid and benzene acetic acid are the products of degradation identified based on thin layer chromatography, high performance liquid chromatography, gas chromatography and mass analyses. It has been observed that the degradation is initiated by the biosurfactant of the isolate for solubilization through micellation and then the alkali pH and intra/extra cellular degradative enzymes accomplish the degradation process. Encoding of genes responsible for biosurfactant production (licA3 as well as catabolic reactions (C23O made with suitable primers designed. The study concludes in situ production of biosurfactant mediates the degradation of anthracene by B. licheniformis.

  17. Binary metal oxide nanoparticle incorporated composite multilayer thin films for sono-photocatalytic degradation of organic pollutants

    Science.gov (United States)

    Gokul, Paramasivam; Vinoth, Ramalingam; Neppolian, Bernaurdshaw; Anandhakumar, Sundaramurthy

    2017-10-01

    We report reduced graphene oxide (rGO) supported binary metal oxide (CuO-TiO2/rGO) nanoparticle (NP) incorporated multilayer thin films based on Layer-by-Layer (LbL) assembly for enhanced sono-photocatalytic degradation of methyl orange under exposure to UV radiation. Multilayer thin films were fabricated on glass and quartz slides, and investigated using scanning electron microscopy and UV-vis spectroscopy. The loading of catalyst NPs on the film resulted in the change of morphology of the film from smooth to rough with uniformly distributed NPs on the surface. The growth of the control and NP incorporated films followed a linear regime as a function of number of layers. The%degradation of methyl orange as a function of time was investigated by UV-vis spectroscopy and total organic carbon (TOC) measurements. Complete degradation of methyl orange was achieved within 13 h. The amount of NP loading in the film significantly influenced the%degradation of methyl orange. Catalyst reusability studies revealed that the catalyst thin films could be repeatedly used for up to five times without any change in photocatalytic activity of the films. The findings of the present study support that the binary metal oxide catalyst films reported here are very useful for continuous systems, and thus, making it an option for scale up.

  18. Draft Genome Sequence of MCPA-Degrading Sphingomonas sp. Strain ERG5, Isolated from a Groundwater Aquifer in Denmark

    DEFF Research Database (Denmark)

    Nielsen, Tue Kjærgaard; Kot, Witold; Sørensen, Sebastian R

    2015-01-01

    Sphingomonas sp. strain ERG5 was isolated from a bacterial community, originating from a groundwater aquifer polluted with low pesticide concentrations. This bacterium degrades 2-methyl-4-chlorophenoxyacetic acid (MCPA) in a wide spectrum of concentrations and has been shown to function in bioaug...

  19. Installation of site-specific methylation into histones using methyl lysine analogs.

    Science.gov (United States)

    Simon, Matthew D

    2010-04-01

    Chromatin structure is influenced by post-translational modifications on histones, the principal basic protein component of chromatin. In order to study one of these modifications, lysine methylation, in the context of reconstituted chromatin, this unit describes the installation of analogs of methyl lysine residues into recombinant histones. The modification site is specified by mutating the lysine of interest to cysteine. The mutant histones are expressed and purified, and the cysteine residue alkylated to produce N-methyl aminoethylcysteine, an isosteric analog of methyl lysine. Using different alkylating reagents, it is possible to install analogs of mono-, di-, or trimethyl lysine. While these analogs are not identical to methyl lysine residues, they show similar biochemical properties to their natural counterparts. The ease of synthesis of methyl lysine analog (MLA) histones, especially on a large scale, makes them particularly useful reagents for studying the effects of histone lysine methylation on chromatin structure, biophysics and biochemistry. (c) 2010 by John Wiley & Sons, Inc.

  20. Whole-genome DNA methylation profiling using MethylCap-seq.

    Science.gov (United States)

    Brinkman, Arie B; Simmer, Femke; Ma, Kelong; Kaan, Anita; Zhu, Jingde; Stunnenberg, Hendrik G

    2010-11-01

    MethylCap-seq is a robust procedure for genome-wide profiling of DNA methylation. The approach consists of the capture of methylated DNA using the MBD domain of MeCP2, and subsequent next-generation sequencing of eluted DNA. Elution of the captured methylated DNA is done in steps using a salt gradient, which stratifies the genome into fractions with different CpG density. The enrichment reached within the individual eluates allows for cost-effective deep sequence coverage. The profiles together yield a detailed genome-wide map of methylated regions and readily allows detection of DNA methylation in known and novel regions. Here, we describe principles and details of the MethylCap-seq procedure using different sources of starting material. Copyright © 2010 Elsevier Inc. All rights reserved.

  1. DNA methylation profiling using the methylated-CpG island recovery assay (MIRA).

    Science.gov (United States)

    Rauch, Tibor A; Pfeifer, Gerd P

    2010-11-01

    The methylated-CpG island recovery assay (MIRA) exploits the intrinsic specificity and the high affinity of a methylated-CpG-binding protein complex (MBD2B and MBD3L1) to methylated CpG dinucleotides in genomic DNA. The MIRA approach works on double-stranded DNA and does not depend on the application of methylation-sensitive restriction enzymes. It can be performed on a few hundred nanograms of genomic DNA. Recently, the MIRA technique has been used to profile DNA methylation patterns at a resolution of 100 base pairs along the entire genome of normal human B-lymphocytes. The MIRA method is compatible with microarray and next generation DNA sequencing approaches. We describe the principles and details of this method applied for methylation profiling of genomes containing methylated CpG sequences.

  2. ASSAYING OF AUTOPHAGIC PROTEIN DEGRADATION

    NARCIS (Netherlands)

    C. Bauvy; A.J. Meijer; P. Codogno

    2009-01-01

    Macroautophagy is a three-step process: (1) autophagosomes form and mature, (2) the autophagosomes fuse with lysosomes, and (3) the autophagic cargo is degraded in the lysosomes. It is this lysosomal degradation of the autophagic cargo that constitutes the autophagic flux. As in the case of metaboli

  3. MOSFET Degradation Under RF Stress

    NARCIS (Netherlands)

    Sasse, G.T.; Kuper, F.G.; Schmitz, Jurriaan

    2008-01-01

    We report on the degradation of MOS transistors under RF stress. Hot-carrier degradation, negative-bias temperature instability, and gate dielectric breakdown are investigated. The findings are compared to established voltage- and field-driven models. The experimental results indicate that the

  4. Profiling genome-wide DNA methylation.

    Science.gov (United States)

    Yong, Wai-Shin; Hsu, Fei-Man; Chen, Pao-Yang

    2016-01-01

    DNA methylation is an epigenetic modification that plays an important role in regulating gene expression and therefore a broad range of biological processes and diseases. DNA methylation is tissue-specific, dynamic, sequence-context-dependent and trans-generationally heritable, and these complex patterns of methylation highlight the significance of profiling DNA methylation to answer biological questions. In this review, we surveyed major methylation assays, along with comparisons and biological examples, to provide an overview of DNA methylation profiling techniques. The advances in microarray and sequencing technologies make genome-wide profiling possible at a single-nucleotide or even a single-cell resolution. These profiling approaches vary in many aspects, such as DNA input, resolution, genomic region coverage, and bioinformatics analysis, and selecting a feasible method requires knowledge of these methods. We first introduce the biological background of DNA methylation and its pattern in plants, animals and fungi. We present an overview of major experimental approaches to profiling genome-wide DNA methylation and hydroxymethylation and then extend to the single-cell methylome. To evaluate these methods, we outline their strengths and weaknesses and perform comparisons across the different platforms. Due to the increasing need to compute high-throughput epigenomic data, we interrogate the computational pipeline for bisulfite sequencing data and also discuss the concept of identifying differentially methylated regions (DMRs). This review summarizes the experimental and computational concepts for profiling genome-wide DNA methylation, followed by biological examples. Overall, this review provides researchers useful guidance for the selection of a profiling method suited to specific research questions.

  5. Comparison of pH-sensitive degradability of maleic acid amide derivatives.

    Science.gov (United States)

    Kang, Sunyoung; Kim, Youngeun; Song, Youngjun; Choi, Jin Uk; Park, Euddeum; Choi, Wonmin; Park, Jeongseon; Lee, Yan

    2014-05-15

    We synthesized five maleic acid amide derivatives (maleic, citraconic, cis-aconitic, 2-(2'-carboxyethyl) maleic, 1-methyl-2-(2'-carboxyethyl) maleic acid amide), and compared their degradability for the future development of pH-sensitive biomaterials with tailored kinetics of the release of drugs, the change of charge density, and the degradation of scaffolds. The degradation kinetics was highly dependent upon the substituents on the cis-double bond. Among the maleic acid amide derivatives, 2-(2'-carboxyethyl) maleic acid amide with one carboxyethyl and one hydrogen substituent showed appropriate degradability at weakly acidic pH, and the additional carboxyl group can be used as a pH-sensitive linker.

  6. Degradation of the Pesticides Mecoprop and Atrazine in Unpolluted Sandy Aquifers

    DEFF Research Database (Denmark)

    Klint, Mikala; Arvin, Erik; Jensen, Bjørn K.

    1993-01-01

    The potential for biodegradation of the pesticides mecoprop ((+/-)-2-(4-chloro-2-methyl-phenoxy)propionic acid) and atrazine (2-chloro-4-ethylamino-6-isopropylamino-s-triazine) in an aerobic aquifer was investigated in laboratory batch experiments. The experiments were performed with groundwater...... and suspensions of groundwater and aquifer sediment collected from a pristine sandy aquifer. Following a lag period of 35 to 40 d, mecoprop in a concentration of 100 mu-g/L was degraded in 30 d in groundwater at 10 degree C. New additions of 100 to 140 mu-g mecoprop/L were degraded within a week. In suspensions...... of groundwater and aquifer sediment, mecoprop in the concentration range 75 to 300 mu-g/L was degraded in 15 d, following a lag period of less than 7 d. Experiments performed with sediments taken from different depths indicate that there was a considerable variation in the degradation potential within...

  7. Singlet oxygen mediated DNA degradation by copper nanoparticles: potential towards cytotoxic effect on cancer cells

    Science.gov (United States)

    2011-01-01

    The DNA degradation potential and anti-cancer activities of copper nanoparticles of 4-5 nm size are reported. A dose dependent degradation of isolated DNA molecules by copper nanoparticles through generation of singlet oxygen was observed. Singlet oxygen scavengers such as sodium azide and Tris [hydroxyl methyl] amino methane were able to prevent the DNA degradation action of copper nanoparticles confirming the involvement of activated oxygen species in the degradation process. Additionally, it was observed that the copper nanoparticles are able to exert cytotoxic effect towards U937 and Hela cells of human histiocytic lymphoma and human cervical cancer origins, respectively by inducing apoptosis. The growth characteristics of U937 and Hela cells were studied applying various concentrations of the copper nanoparticles. PMID:21439072

  8. Preparation and photocatalytic degradation performance of Ag3PO4 with a two-step approach

    Science.gov (United States)

    Li, Jiwen; Ji, Xiaojing; Li, Xian; Hu, Xianghua; Sun, Yanfang; Ma, Jingjun; Qiao, Gaowei

    2016-05-01

    Ag3PO4 photocatalysts were prepared via two and one-step through a facile ion-exchange route. The photocatalysts were then characterized through powder X-ray diffraction, scanning electron microscopy and UV-vis diffuse reflectance spectroscopy. The photocatalytic activity of the samples was evaluated on the basis of the photocatalytic degradation of methyl orange (MO) and methylene blue (MB) under solar irradiation. The MO degradation rate of the Photocatalyst synthesized by the two-step ion-exchange route was 89.18% in 60 min. This value was four times that of the Photocatalyst synthesized by the one-step approach.The MB degradation rate was 97% in 40 min. After six cycling runs were completed, the MO degradation rate was 73%

  9. Kinetics of sonophotocatalytic degradation of anionic dyes with Nano-TiO2.

    Science.gov (United States)

    Vinu, R; Madras, Giridhar

    2009-01-15

    The current research work focuses on the combination of photocatalytic and sonocatalytic (sonophotocatalytic) degradation of anionic dyes, viz., Orange G, Remazol Brilliant Blue R, Alizarin Red S, Methyl Blue, and Indigo Carmine, with solution combustion synthesized TiO2 (CS TiO2) and commercial Degussa P-25 TiO2 (DP-25). The rate of sonophotocatalytic degradation of all the dyes and the reduction of total organic carbon was higher compared to the individual photo- and sonocatalytic processes. The effect of dissolved gases and ultrasonic intensity on the sonophotocatalytic degradation of the dyes was evaluated. A dual-pathway network mechanism of sonophotocatalytic degradation was proposed for the first time, and the rate equations were modeled using the network reduction technique. The kinetic rate coefficients of the individual steps were evaluated for all the systems by fitting the model with experimental data.

  10. Fast degradation of dyes in water using manganese-oxide-coated diatomite for environmental remediation

    Science.gov (United States)

    Dang, Trung-Dung; Banerjee, Arghya Narayan; Tran, Quang-Tung; Roy, Sudipta

    2016-11-01

    By a simple wet-chemical procedure using a permanganate in the acidic medium, diatomite coated with amorphous manganese oxide nanoparticles was synthesized. The structural, microstructural and morphological characterizations of the as-synthesized catalysts confirmed the nanostructure of MnO2 and its stabilization on the support - diatomite. The highly efficient and rapid degradation of methylene blue and methyl orange over synthesized MnO2 coated Diatomite has been carried out. The results revealed considerably faster degradation of the dyes against the previously reported data. The proposed mechanism of the dye-degradation is considered to be a combinatorial effect of chemical, physicochemical and physical processes. Therefore, the fabricated catalysts have potential application in waste water treatment, and pollution degradation for environmental remediation.

  11. Preparation and Photocatalytic Performance of MWCNTs/TiO2 Nanocomposites for Degradation of Aqueous Substrate

    Directory of Open Access Journals (Sweden)

    Qiannan Duan

    2016-01-01

    Full Text Available In this study, multiwalled carbon nanotubes (MWCNTs/TiO2 nanocomposites were obtained by constant volumetric wet impregnation processes. The prepared catalysts were characterized by scanning electron microscopy (SEM and X-ray photoelectron spectroscopy (XPS. The effect of reaction conditions on photocatalytic performance of the catalysts was investigated by the degradation of methyl orange (MO under UV irradiation, in a new type of reactor with unique structure. The results showed that the prepared nanocomposite exhibited higher MO degradation efficiency than that of pure nano-TiO2. Besides, in batch experiments of influencing factors, including ionic strength, oxidant amount, and response times, the presence of H2O2 would contribute to increasing the MO degradation rate of MWCNTs/TiO2 samples. Ionic concentration and long reaction times are adverse to the MO degradation in the processes.

  12. Molecular analysis of methanogens involved in methanogenic degradation of tetramethylammonium hydroxide in full-scale bioreactors.

    Science.gov (United States)

    Whang, Liang-Ming; Hu, Tai-Ho; Liu, Pao-Wen Grace; Hung, Yu-Ching; Fukushima, Toshikazu; Wu, Yi-Ju; Chang, Shao-Hsiung

    2015-02-01

    This study investigated methanogenic communities involved in degradation of tetramethylammonium hydroxide (TMAH) in three full-scale bioreactors treating TMAH-containing wastewater. Based on the results of terminal-restriction fragment-length polymorphism (T-RFLP) and quantitative PCR analyses targeting the methyl-coenzyme M reductase alpha subunit (mcrA) genes retrieved from three bioreactors, Methanomethylovorans and Methanosarcina were the dominant methanogens involved in the methanogenic degradation of TMAH in the bioreactors. Furthermore, batch experiments were conducted to evaluate mcrA messenger RNA (mRNA) expression during methanogenic TMAH degradation, and the results indicated that a higher level of TMAH favored mcrA mRNA expression by Methansarcina, while Methanomethylovorans could only express considerable amount of mcrA mRNA at a lower level of TMAH. These results suggest that Methansarcina is responsible for methanogenic TMAH degradation at higher TMAH concentrations, while Methanomethylovorans may be important at a lower TMAH condition.

  13. Singlet oxygen mediated DNA degradation by copper nanoparticles: potential towards cytotoxic effect on cancer cells

    Directory of Open Access Journals (Sweden)

    Sengupta Tapas K

    2011-03-01

    Full Text Available Abstract The DNA degradation potential and anti-cancer activities of copper nanoparticles of 4-5 nm size are reported. A dose dependent degradation of isolated DNA molecules by copper nanoparticles through generation of singlet oxygen was observed. Singlet oxygen scavengers such as sodium azide and Tris [hydroxyl methyl] amino methane were able to prevent the DNA degradation action of copper nanoparticles confirming the involvement of activated oxygen species in the degradation process. Additionally, it was observed that the copper nanoparticles are able to exert cytotoxic effect towards U937 and Hela cells of human histiocytic lymphoma and human cervical cancer origins, respectively by inducing apoptosis. The growth characteristics of U937 and Hela cells were studied applying various concentrations of the copper nanoparticles.

  14. Enantioselective Degradation of Rac-Metolachlor and S-Metolachlor in Soil

    Institute of Scientific and Technical Information of China (English)

    MA Yun; LIU Wei-Ping; WEN Yue-Zhong

    2006-01-01

    Separation of chiral enantiomers and the dissipation of rac-metolachlor and S-metolachlor in soil were evaluated using achiral high-performance liquid chromatography (HPLC) and chiral gas chromatography (GC) methods. Under the experimental conditions the possible metabolite was considered to be N-(2-ethyl-6-methyl-phenyl)-2-hydroxy-acetamide.Because of the presence of two chiral elements (asymmetrically substituted carbon and chiral axis), the baseline separation of metolachlor enantiomers was not achieved. S-metolachlor degraded faster in soil than rac-metolachlor. After a 42-day incubation, 73.4% of rac-metolachlor and 90.0% of S-metolachlor were degraded. However, due to the absence of biological processes the degradation process in sterilized soil showed no enantioselectivity. The results indicated that enantioselective degradations could greatly affect the environmental fate of metolachlor and should be considered when the environmental behavior of these compounds was assessed.

  15. Free radical polymers with tunable and selective bio- and chemical degradability.

    Science.gov (United States)

    Paulusse, Jos M J; Amir, Roey J; Evans, Richard A; Hawker, Craig J

    2009-07-22

    A versatile synthetic strategy has been developed which enables the facile incorporation of cleavable functional groups, i.e., esters, thioesters, and disulfides, into the carbon-carbon backbone of vinyl-based polymers. Through the synthesis of novel cyclic monomers, RAFT-mediated radical ring-opening copolymerizations with traditional vinyl monomers such as methyl methacrylate, N,N-dimethylaminoethyl methacrylate, and 2-hydroxyethyl methacrylate lead to the introduction of controlled degradability into these widely used vinyl copolymer systems. An additional benefit of this strategy is the inherent versatility available through the incorporation of cyclic monomers containing diverse functional groups such as esters, thioesters, disulfides, and silyl ether units that allow degradation under basic/acidic, reductive, or enzymatic conditions. By integrating multiple, orthogonal cyclic monomers into linear copolymer backbones, well-defined systems with programmable degradation profiles are obtained which allows for tunable, selective, and stepwise degradation of the vinyl polymer backbones.

  16. Biodegradation of Methyl tert-Butyl Ether by Co-Metabolism with a Pseudomonas sp. Strain

    Directory of Open Access Journals (Sweden)

    Shanshan Li

    2016-09-01

    Full Text Available Co-metabolic bioremediation is supposed to be an impressive and promising approach in the elimination technology of methyl tert-butyl ether (MTBE, which was found to be a common pollutant worldwide in the ground or underground water in recent years. In this paper, bacterial strain DZ13 (which can co-metabolically degrade MTBE was isolated and named as Pseudomonas sp. DZ13 based on the result of 16S rRNA gene sequencing analysis. Strain DZ13 could grow on n-alkanes (C5-C8, accompanied with the co-metabolic degradation of MTBE. Diverse n-alkanes with different carbon number showed a significant influence on the degradation rate of MTBE and accumulation of tert-butyl alcohol (TBA. When Pseudomonas sp. DZ13 co-metabolically degraded MTBE with n-pentane as the growth substrate, a higher MTBE-degrading rate (Vmax = 38.1 nmol/min/mgprotein, Ks = 6.8 mmol/L and lower TBA-accumulation was observed. In the continuous degradation experiment, the removal efficiency of MTBE by Pseudomonas sp. Strain DZ13 did not show an obvious decrease after five times of continuous addition.

  17. Enzymatic degradation of endomorphins.

    Science.gov (United States)

    Janecka, Anna; Staniszewska, Renata; Gach, Katarzyna; Fichna, Jakub

    2008-11-01

    Centrally acting plant opiates, such as morphine, are the most frequently used analgesics for the relief of severe pain, even though their undesired side effects are serious limitation to their usefulness. The search for new therapeutics that could replace morphine has been mainly focused on the development of peptide analogs or peptidomimetics with high selectivity for one receptor type and high bioavailability, that is good blood-brain barrier permeability and enzymatic stability. Drugs, in order to be effective, must be able to reach the target tissue and to remain metabolically stable to produce the desired effects. The study of naturally occurring peptides provides a rational and powerful approach in the design of peptide therapeutics. Endogenous opioid peptides, endomorphin-1 and endomorphin-2, are two potent and highly selective mu-opioid receptor agonists, discovered only a decade ago, which display potent analgesic activity. However, extensive studies on the possible use of endomorphins as analgesics instead of morphine met with failure due to their instability. This review deals with the recent investigations that allowed determine degradation pathways of endomorphins in vitro and in vivo and propose modifications that will lead to more stable analogs.

  18. Bacterial degradation of aminopyrine.

    Science.gov (United States)

    Blecher, H; Blecher, R; Wegst, W; Eberspaecher, J; Lingens, F

    1981-11-01

    1. Four strains of bacteria growing with aminopyrine as sole source of carbon were isolated from soil and were identified as strains of Phenylobacterium immobilis. 2. Strain M13 and strain E, the type species of Phenylobacterium immobilis (DSM 1986), which had been isolated by enrichment with chloridazon (5-amino-4-chloro-2-phenyl-2H-pyridazin-3-one) were used to investigate the bacterial degradation of aminopyrine. 3. Three metabolites were isolated and identified as: 4-(dimethylamino)-1,2-dihydro-1,5-dimethyl-2-(2,3-dihydro-2,3-dihydroxy-4,6-cyc lohexadien-1-yl)-3H-pyrazol-3-one, 4-(dimethylamino)-1,2-dihydro-1,5-dimethyl-2-(2,3-dihydroxyphenyl)-3H-pyrazol-3 -one and 4-(dimethylamino)-1,2-dihydro-1,5-dimethyl-3H-pyrazol-3-one. 4. An enzyme extract from cells of strain m13 was shown to further metabolize the catechol derivative of aminopyrine, with the formation of 2-pyrone-6-carboxylic acid. 5. Results indicate that the benzene ring of aminopyrine is the principal site of microbial metabolism.

  19. Fabrication of Pentacene Thin-Film Transistors with Patterned Polyimide Photoresist as Gate Dielectrics and Research of Their Degradation

    Institute of Scientific and Technical Information of China (English)

    LIANG Yan; DONG Gui-Fang; HU Yuan-Chuan; HU Yan; WANG Li-Duo; QIU Yong

    2004-01-01

    @@ Pentacene organic thin-film transistors using commercial photoresist as gate dielectrics were fabricated. The photoresist was spin-coated and directly patterned by photolithography. As a result, the fabrication processes were greatly reduced. With the characteristics of the transistors measured, the degradation of the transistors was investigated. In the search for the factors causing degradation, a transistor using poly(methyl methacrylate)as the gate dielectric was also fabricated. It is regarded that the degradation is caused by the changes at the interface between photoresist and pentacene film.

  20. Activity, biomass and composition of microbial communities and their degradation pathways in exposed propazine soil.

    Science.gov (United States)

    Jiang, Chen; Lu, Yi Chen; Xu, Jiang Yan; Song, Yang; Song, Yue; Zhang, Shu Hao; Ma, Li Ya; Lu, Feng Fan; Wang, Ya Kun; Yang, Hong

    2017-11-01

    Propazine is a s-triazine herbicide widely used for controlling weeds for crop production. Its persistence and contamination in environment nagatively affect crop growth and food safety. Elimination of propazine residues in the environment is critical for safe crop production. This study identified a microbial community able to degrade propazine in a farmland soil. About 94% of the applied propazine was degraded within 11 days of incubation when soil was treated with 10mgkg(-1) propazine as the initial concentration. The process was accompanied by increased microbial biomass and activities of soil enzymes. Denaturing gradient gel electrophoresis (DGGE) revealed multiple bacterial strains in the community as well as dynamic change of the composition of microbial community with a reduced microbial diversity (H' from 3.325 to 2.78). Tracking the transcript level of degradative genes AtzB, AtzC and TrzN showed that these genes were induced by propazine and played important roles in the degradation process. The activities of catalase, dehydrogenase and phenol oxidase were stimulated by propazine exposure. Five degradation products (hydroxyl-, methylated-, dimeric-propazine, ammeline and ammelide) were characterized by UPLC-MS(2), revealing a biodegradation of propazine in soil. Several novel methylated and dimeric products of propazine were characterized in thepropazine-exposed soil. These data help understand the pathway, detailed mechanism and efficiency of propazine biodegradation in soil under realistic field condition. Copyright © 2017 Elsevier Inc. All rights reserved.